#description: "HPO annotations for rare diseases [8348: OMIM; 47: DECIPHER; 4316 ORPHANET]"
#version: 2025-10-22
#tracker: https://github.com/obophenotype/human-phenotype-ontology/issues
#hpo-version: http://purl.obolibrary.org/obo/hp/releases/2025-10-22/hp.json
database_id	disease_name	qualifier	hpo_id	reference	evidence	onset	frequency	sex	modifier	aspect	biocuration
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0011097	PMID:31675180	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0001518	PMID:31675180	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0032792	PMID:31675180	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0011451	PMID:31675180	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0010851	PMID:31675180	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0001789	PMID:31675180	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0200134	PMID:31675180	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0001522	PMID:31675180	PCS		1/2			C	HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0000006	PMID:31675180	PCS					I	HPO:probinson[2021-06-21];HPO:probinson[2021-06-21]
OMIM:619340	Developmental and epileptic encephalopathy 96		HP:0002643	PMID:31675180	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:609153	Pseudohyperkalemia, familial, 2, due to red cell leak		HP:0002378	PMID:2766660	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:609153	Pseudohyperkalemia, familial, 2, due to red cell leak		HP:0003324	PMID:2766660	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:609153	Pseudohyperkalemia, familial, 2, due to red cell leak		HP:0002153	OMIM:609153	TAS					P	HPO:lccarmody[2018-10-03];HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-14]
OMIM:609153	Pseudohyperkalemia, familial, 2, due to red cell leak		HP:0003394	PMID:2766660	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:609153	Pseudohyperkalemia, familial, 2, due to red cell leak		HP:0001878	PMID:24947683	PCS		0/2			P	HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-14]
OMIM:609153	Pseudohyperkalemia, familial, 2, due to red cell leak		HP:0003768	PMID:2766660	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:609153	Pseudohyperkalemia, familial, 2, due to red cell leak		HP:0000006	PMID:24947683	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-14]
OMIM:614102	Immunoglobulin kappa light chain deficiency		HP:0002014	OMIM:614102	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614102	Immunoglobulin kappa light chain deficiency		HP:6000261	PMID:26853951	PCS		1/1			P	HPO:probinson[2024-02-09]
OMIM:614102	Immunoglobulin kappa light chain deficiency		HP:0002719	PMID:3931219	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-22]
OMIM:614102	Immunoglobulin kappa light chain deficiency		HP:0011463	PMID:26853951	PCS		1/1			C	HPO:probinson[2023-01-22]
OMIM:614102	Immunoglobulin kappa light chain deficiency		HP:0000007	PMID:3931219	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614102	Immunoglobulin kappa light chain deficiency		HP:0002205	PMID:26853951	PCS		1/1			P	HPO:probinson[2023-01-22]
OMIM:614102	Immunoglobulin kappa light chain deficiency		HP:0002028	PMID:26853951	PCS		1/1			P	HPO:probinson[2023-01-22]
OMIM:619426	White-Kernohan syndrome		HP:0000286	PMID:33743206	PCS		3/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0010804	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0006989	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0001252	PMID:33743206	PCS		7/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0003196	PMID:33743206	PCS		4/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0003593	PMID:33743206	PCS		5/8			C	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000085	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0002020	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0012745	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000639	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0011463	PMID:33743206	PCS		1/8			C	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0020045	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000637	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000278	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0001249	PMID:33743206	PCS		8/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0020206	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0001385	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000574	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0002870	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000293	PMID:33743206	PCS		5/8			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0001382	PMID:33743206	PCS		4/8			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0011800	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0011330	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000601	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000403	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000527	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000400	PMID:33743206	PCS		5/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000006	PMID:33743206	TAS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000369	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000126	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000143	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000582	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000463	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0034003	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-10-03]
OMIM:619426	White-Kernohan syndrome		HP:0000739	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000219	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000537	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0001545	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000154	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0003621	PMID:33743206	PCS		2/8			C	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000430	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000072	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0005280	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0011228	PMID:33743206	PCS		3/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000506	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000821	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0000664	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0007018	PMID:33743206	PCS		1/8			P	HPO:probinson[2021-08-22]
OMIM:619426	White-Kernohan syndrome		HP:0001513	PMID:33743206	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:610370	Diarrhea 4, malabsorptive, congenital		HP:0002014	OMIM:610370	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610370	Diarrhea 4, malabsorptive, congenital		HP:0002013	OMIM:610370	IEA					P	HPO:iea[2009-02-17]
OMIM:610370	Diarrhea 4, malabsorptive, congenital		HP:0001508	OMIM:610370	IEA					P	HPO:iea[2009-02-17]
OMIM:610370	Diarrhea 4, malabsorptive, congenital		HP:0004918	OMIM:610370	IEA					P	HPO:iea[2009-02-17]
OMIM:610370	Diarrhea 4, malabsorptive, congenital		HP:0001944	OMIM:610370	IEA					P	HPO:iea[2009-02-17]
OMIM:610370	Diarrhea 4, malabsorptive, congenital		HP:0000007	OMIM:610370	IEA					I	HPO:iea[2009-02-17]
OMIM:610370	Diarrhea 4, malabsorptive, congenital		HP:0003623	OMIM:610370	IEA					C	HPO:iea[2009-02-17]
OMIM:609621	Short QT syndrome 2		HP:0012232	PMID:15890322	PCS					P	HPO:probinson[2013-01-09]
OMIM:609621	Short QT syndrome 2		HP:0001663	OMIM:609621	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:609621	Short QT syndrome 2		HP:0001662	OMIM:609621	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609621	Short QT syndrome 2		HP:0005110	PMID:15890322	PCS					P	HPO:probinson[2013-03-31]
OMIM:609621	Short QT syndrome 2		HP:0001279	PMID:15890322	PCS					P	HPO:probinson[2013-03-31]
OMIM:609621	Short QT syndrome 2		HP:0001645	PMID:15890322	PCS					P	HPO:probinson[2013-03-31]
OMIM:609621	Short QT syndrome 2		HP:0000006	PMID:15890322	PCS					I	HPO:probinson[2013-03-31]
OMIM:212790	Premature centromere division		HP:0001939	OMIM:212790	IEA					P	HPO:iea[2009-02-17]
OMIM:212790	Premature centromere division		HP:0000007	OMIM:212790	IEA					I	HPO:iea[2009-02-17]
OMIM:212790	Premature centromere division		HP:0003745	OMIM:212790	TAS					I	HPO:skoehler[2015-12-30]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0000143	PMID:19890111	PCS	HP:0003593	1/1	FEMALE		P	HPO:probinson[2013-03-12];HPO:probinson[2020-11-01]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0004387	PMID:19890111	PCS	HP:0003593	2/2			P	HPO:probinson[2013-03-12];HPO:probinson[2020-11-01]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0003593	PMID:21519361;PMID:19890111	PCS		3/3			C	HPO:probinson[2022-02-27]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0033279	PMID:19890111	PCS		1/2			P	HPO:probinson[2020-12-07]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0000007	PMID:19890111	PCS					I	HPO:probinson[2013-03-12];HPO:probinson[2020-11-01]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0033256	PMID:21519361	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0002837	PMID:21519361	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0009789	PMID:19890111	PCS	HP:0003593	1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2020-11-01]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0025084	PMID:19890111	PCS	HP:0003593	2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-11-01]
OMIM:612567	Inflammatory bowel disease 25, early onset, autosomal recessive		HP:0025084	PMID:21519361	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:613679	Congenital prothrombin deficiency		HP:0000132	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0003577	OMIM:613679	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0003010	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0031364	OMIM:613679	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613679	Congenital prothrombin deficiency		HP:0005261	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0008151	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0003828	OMIM:613679	TAS					M	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0000007	PMID:7740448	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2019-01-21]
OMIM:613679	Congenital prothrombin deficiency		HP:0000978	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0000421	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0002239	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0000225	OMIM:613679	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613679	Congenital prothrombin deficiency		HP:0003645	OMIM:613679	TAS					P	HPO:skoehler[2012-12-03]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0001265	OMIM:614116	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0003676	OMIM:614116	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0002059	OMIM:614116	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000365	OMIM:614116	TAS	HP:0011462	16/18			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-04-03]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0002354	OMIM:614116	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0001262	OMIM:614116	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0002460	PMID:21532572	PCS		2/18			P	HPO:probinson[2023-04-03]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0001251	PMID:21532572	PCS		4/18			P	HPO:probinson[2023-04-03]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0003380	OMIM:614116	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0031258	OMIM:614116	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0100710	OMIM:614116	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000737	OMIM:614116	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000407	OMIM:614116	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000726	PMID:21532572	PCS	HP:0003581	18/18			P	HPO:skoehler[2012-11-20]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000726	OMIM:614116	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0011462	PMID:21532572	PCS		18/18			C	HPO:probinson[2023-04-03]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000741	OMIM:614116	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000763	PMID:21532572	PCS		18/18			P	HPO:skoehler[2012-11-20]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0000006	PMID:21532572	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:614116	Neuropathy, hereditary sensory, type IE		HP:0002754	OMIM:614116	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0003596	PMID:18614783	PCS		5/11			C	HPO:probinson[2022-07-09]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0031295	PMID:18614783	PCS		7/11			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0011462	PMID:18614783	PCS		6/11			C	HPO:probinson[2022-07-09]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0005110	PMID:18614783	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-09]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0001712	PMID:18614783	PCS		0/11			P	HPO:probinson[2022-07-09]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0012664	PMID:18614783	PCS		0/11			P	HPO:probinson[2022-07-09]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0000006	PMID:18614783	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-07-09]
OMIM:612201	Atrial fibrillation, familial, 6		HP:0034307	PMID:18614783	PCS		5/11			P	HPO:probinson[2022-09-05]
OMIM:137580	Gilles de la tourette syndrome		HP:0010529	OMIM:137580	IEA					P	HPO:skoehler[2010-06-18]
OMIM:137580	Gilles de la tourette syndrome		HP:0000718	OMIM:137580	TAS					P	HPO:skoehler[2013-02-25]
OMIM:137580	Gilles de la tourette syndrome		HP:0000722	OMIM:137580	IEA					P	HPO:iea[2009-02-17]
OMIM:137580	Gilles de la tourette syndrome		HP:0100035	OMIM:137580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:137580	Gilles de la tourette syndrome		HP:0007018	OMIM:137580	IEA					P	HPO:iea[2009-02-17]
OMIM:137580	Gilles de la tourette syndrome		HP:0000006	OMIM:137580	IEA					I	HPO:iea[2009-02-17]
OMIM:137580	Gilles de la tourette syndrome		HP:0000742	OMIM:137580	IEA					P	HPO:iea[2009-02-17]
OMIM:137580	Gilles de la tourette syndrome		HP:0100034	OMIM:137580	TAS					P	HPO:skoehler[2015-01-21]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0003577	PMID:32500975	PCS		3/3			C	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000486	PMID:32500975	PCS		2/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000365	PMID:32500975	PCS	HP:0003577	3/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0009938	PMID:32500975	PCS		3/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0007618	PMID:32500975	PCS		3/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0001271	PMID:32500975	PCS		2/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000272	PMID:32500975	PCS		3/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0011344	PMID:32500975	PCS		2/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0100830	PMID:32500975	PCS		1/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0011343	PMID:32500975	PCS		1/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000729	PMID:32500975	PCS		2/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000519	PMID:32500975	PCS		3/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000007	PMID:32500975	PCS					I	HPO:probinson[2021-08-18];HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000664	PMID:32500975	PCS		1/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000322	PMID:32500975	PCS		2/3			P	HPO:probinson[2021-08-18]
OMIM:619354	Deafness, cataract, impaired intellectual development, and polyneuropathy		HP:0000336	PMID:32500975	PCS		3/3			P	HPO:probinson[2021-08-18]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0002025	PMID:25047197	PCS		1/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000286	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001374	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0005257	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000086	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0002020	OMIM:117650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000162	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000085	OMIM:117650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0410030	PMID:25047197	PCS		1/16			P	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0006593	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0008897	OMIM:117650	TAS					P	HPO:skoehler[2012-10-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000878	OMIM:117650	TAS		2/16			P	HPO:probinson[2015-02-21];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001643	OMIM:117650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0010290	OMIM:117650	TAS					P	HPO:skoehler[2010-06-18]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001249	PMID:25047197	PCS		3/15			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000358	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000252	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000175	PMID:25047197	PCS		10/15			P	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000494	PMID:25047197	PCS		3/16			P	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0004695	OMIM:117650	TAS					P	HPO:probinson[2015-02-21]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0030300	PMID:25047197	PCS		2/16			P	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0004209	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000405	PMID:25047197	PCS		6/16			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0002987	OMIM:117650	TAS					P	HPO:probinson[2015-02-21]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000201	PMID:25047197	PCS		14/16			P	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000006	PMID:25047197	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000369	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001611	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0004468	OMIM:117650	TAS					P	HPO:probinson[2015-12-21]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0003577	PMID:25047197	PCS		16/16			C	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000343	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001591	PMID:25047197	PCS		7/16			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000185	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0005792	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001629	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000218	PMID:25047197	PCS		5/15			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0030282	PMID:25047197	PCS		10/15			P	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0030280	OMIM:117650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001545	OMIM:117650	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001561	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000670	PMID:25047197	PCS		1/16			P	HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0002650	PMID:25047197	PCS		5/15			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0002132	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000272	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000107	OMIM:117650	TAS					P	HPO:skoehler[2014-01-28]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0001631	PMID:25047197	PCS		3/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000465	PMID:25047197	PCS		1/16			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-02]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0000347	OMIM:117650	TAS				HP:0012828	P	HPO:probinson[2012-04-30]
OMIM:117650	Cerebrocostomandibular syndrome		HP:0002643	OMIM:117650	TAS					P	HPO:probinson[2009-02-17]
OMIM:616067	46,xy sex reversal 9		HP:0003577	PMID:24549039	PCS		2/2			C	HPO:probinson[2022-11-27]
OMIM:616067	46,xy sex reversal 9		HP:0012245	PMID:24549039	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-27]
OMIM:616067	46,xy sex reversal 9		HP:0000133	PMID:24549039	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:616067	46,xy sex reversal 9		HP:0000062	PMID:24549039	PCS		1/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-11-27]
OMIM:616067	46,xy sex reversal 9		HP:0000729	OMIM:616067	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:616067	46,xy sex reversal 9		HP:0000063	PMID:24549039	PCS		1/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-11-27]
OMIM:616067	46,xy sex reversal 9		HP:0000006	PMID:24549039	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-27]
OMIM:108770	Atrial standstill 1		HP:0001706	OMIM:108770	PCS					P	HPO:probinson[2012-04-11]
OMIM:108770	Atrial standstill 1		HP:0025478	PMID:16188595	PCS	HP:0011463	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-04]
OMIM:108770	Atrial standstill 1		HP:0011705	OMIM:108770	PCS					P	HPO:probinson[2012-04-11]
OMIM:108770	Atrial standstill 1		HP:0200127	OMIM:108770	TAS					P	HPO:skoehler[2013-06-11]
OMIM:108770	Atrial standstill 1		HP:0005155	PMID:16188595	PCS	HP:0011463	1/1			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:108770	Atrial standstill 1		HP:0006699	OMIM:108770	PCS					P	HPO:probinson[2012-04-11]
OMIM:108770	Atrial standstill 1		HP:0004757	PMID:16188595	IEA	HP:0011463	1/1			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:108770	Atrial standstill 1		HP:0000006	OMIM:108770	PCS					I	HPO:probinson[2012-04-11]
OMIM:112700	Brachydactyly, type A3		HP:0009370	OMIM:112700	TAS					P	HPO:probinson[2009-02-17]
OMIM:112700	Brachydactyly, type A3		HP:0004220	OMIM:112700	TAS					P	HPO:probinson[2009-02-17]
OMIM:112700	Brachydactyly, type A3		HP:0004209	OMIM:112700	TAS					P	HPO:probinson[2009-02-17]
OMIM:112700	Brachydactyly, type A3		HP:0000006	OMIM:112700	TAS					I	HPO:probinson[2009-02-17]
OMIM:112700	Brachydactyly, type A3		HP:0010579	OMIM:112700	TAS					P	HPO:probinson[2009-02-17]
OMIM:112700	Brachydactyly, type A3		HP:0005910	OMIM:112700	TAS					P	HPO:probinson[2009-02-17]
OMIM:612229	Colorectal cancer, susceptibility to, 3		HP:0003003	PMID:18372901;PMID:17934461;PMID:18372905	PCS					P	HPO:curators[2010-07-08]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000175	PMID:21700882	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-04]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000054	OMIM:614880	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000939	PMID:21700882	PCS		2/7			P	HPO:probinson[2022-12-04]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000938	PMID:21700882	PCS		2/7			P	HPO:probinson[2022-12-04]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000458	PMID:21700882	PCS		7/7			P	HPO:probinson[2022-12-04]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0002857	PMID:21700882	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0012506	OMIM:614880	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0008734	OMIM:614880	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000006	PMID:21700882	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-12-04]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000028	OMIM:614880	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614880	Hypogonadotropic hypogonadism 15 with or without anosmia		HP:0000786	OMIM:614880	TAS					P	HPO:skoehler[2012-11-16]
OMIM:615546	Van maldergem syndrome 2		HP:0000286	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0010804	OMIM:615546	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615546	Van maldergem syndrome 2		HP:0000365	PMID:24056717	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000089	PMID:24056717;PMID:22469822	PCS		6/6			P	HPO:probinson[2023-02-12];HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0001252	PMID:22469822	PCS		2/2			P	HPO:probinson[2023-02-12];HPO:skoehler[2014-11-26];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0012745	OMIM:615546	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615546	Van maldergem syndrome 2		HP:0011220	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000316	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0002779	OMIM:615546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615546	Van maldergem syndrome 2		HP:0001249	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000054	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0002079	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0032409	OMIM:615546	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615546	Van maldergem syndrome 2		HP:0011968	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000293	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0001382	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0001263	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0010554	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0011800	OMIM:615546	TAS					P	HPO:skoehler[2015-11-15]
OMIM:615546	Van maldergem syndrome 2		HP:0009890	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000407	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0010044	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000327	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000007	PMID:24056717	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000689	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000405	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000048	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000047	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000960	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000402	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0004689	OMIM:615546	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615546	Van maldergem syndrome 2		HP:0000341	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0003577	PMID:22469822	PCS		1/1			C	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000023	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0001195	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000260	OMIM:615546	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615546	Van maldergem syndrome 2		HP:0000581	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0010621	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0002282	OMIM:615546	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615546	Van maldergem syndrome 2		HP:0040079	OMIM:615546	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615546	Van maldergem syndrome 2		HP:0000938	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0009487	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0008551	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0030043	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0030084	OMIM:615546	TAS					P	HPO:skoehler[2014-09-21]
OMIM:615546	Van maldergem syndrome 2		HP:0002714	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000218	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0002557	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000774	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000894	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000413	OMIM:615546	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615546	Van maldergem syndrome 2		HP:0001545	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0002652	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0002650	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0001762	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000431	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000272	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0045025	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0032388	PMID:24056717	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0010537	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0005280	PMID:22469822	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000508	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0001510	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615546	Van maldergem syndrome 2		HP:0000028	PMID:22469822	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:615546	Van maldergem syndrome 2		HP:0000347	OMIM:615546	TAS					P	HPO:skoehler[2014-01-28]
OMIM:116200	Cataract 1, multiple types		HP:0100018	PMID:10480374	PCS		10/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-11-27]
OMIM:116200	Cataract 1, multiple types		HP:0003577	PMID:10480374	PCS		10/10			C	HPO:probinson[2022-11-27]
OMIM:116200	Cataract 1, multiple types		HP:0010693	PMID:10480374	PCS	HP:0003577	10/10			P	HPO:probinson[2014-05-22];HPO:probinson[2022-11-27]
OMIM:116200	Cataract 1, multiple types		HP:0000482	OMIM:116200	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:116200	Cataract 1, multiple types		HP:0007787	OMIM:116200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:116200	Cataract 1, multiple types		HP:0000006	PMID:10480374	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-27]
OMIM:607624	Griscelli syndrome, type 2		HP:0002344	OMIM:607624	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:607624	Griscelli syndrome, type 2		HP:0002972	PMID:24134793	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0001250	PMID:10835631	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0002220	PMID:16517541;PMID:10835631	PCS		16/16			P	HPO:probinson[2020-11-06];HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0001010	PMID:24134793	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0003593	PMID:16517541;PMID:24134793	PCS		11/11			C	HPO:probinson[2022-05-30];HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0012156	PMID:16517541;PMID:10835631	PCS		16/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0003819	PMID:24134793	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0002718	PMID:24134793	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0000007	PMID:10835631	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0001008	PMID:24134793	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0002218	PMID:16517541;PMID:10835631	PCS		16/16			P	HPO:probinson[2020-11-06];HPO:iea[2009-02-17];HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0001945	PMID:16517541	PCS		1/1			P	HPO:probinson[2020-11-06]
OMIM:607624	Griscelli syndrome, type 2		HP:0001257	OMIM:607624	IEA					P	HPO:iea[2009-02-17]
OMIM:607624	Griscelli syndrome, type 2		HP:0001433	PMID:16517541	PCS		1/1			P	HPO:probinson[2020-11-06]
OMIM:192100	Uvula, bifid		HP:0000193	OMIM:192100	IEA					P	HPO:iea[2009-02-17]
OMIM:192100	Uvula, bifid		HP:0000006	OMIM:192100	IEA					I	HPO:iea[2009-02-17]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0002650	OMIM:615220	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0004322	OMIM:615220	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0001321	OMIM:615220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0001382	PMID:23499309	PCS		3/9			P	HP:probinson[2019-06-03]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0003023	PMID:23499309	PCS		9/9			P	HP:probinson[2019-06-03]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0000592	PMID:23499309	PCS		6/9			P	HPO:skoehler[2013-06-05];HP:probinson[2019-06-03]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0001263	PMID:23499309	PCS		1/9			P	HPO:skoehler[2013-06-05];HP:probinson[2019-06-03]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0010636	OMIM:615220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0012110	OMIM:615220	TAS					P	HPO:skoehler[2014-09-21]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0000926	OMIM:615220	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0000007	OMIM:615220	TAS					I	HPO:skoehler[2013-06-05]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0002757	PMID:23499309	PCS	HP:0003593	9/9			P	HP:probinson[2019-06-03]
OMIM:615220	Osteogenesis imperfecta, type XV		HP:0000883	OMIM:615220	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0025066	PMID:22031863	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0000980	PMID:22031863	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0002240	PMID:22031863	PCS		1/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0003593	PMID:22031863	PCS		2/3			C	HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0003281	PMID:22031863	PCS		3/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0012463	PMID:22031863	PCS		3/3			P	HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0012465	PMID:22031863	PCS		3/3			P	HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0001903	PMID:22031863	PCS		3/3		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0000957	PMID:22031863	PCS		1/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0011463	PMID:22031863	PCS		1/3			C	HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0032231	PMID:22031863	PCS		3/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0001924	PMID:22031863	PCS		1/3			P	HPO:probinson[2024-02-22]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0001510	PMID:22031863	PCS		1/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0000135	PMID:22031863	PCS		3/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0000006	PMID:22031863	PCS					I	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0001744	PMID:22031863	PCS		1/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0000027	PMID:22031863	PCS		2/2			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-30]
OMIM:615234	Anemia, hypochromic microcytic, with iron overload 2		HP:0004447	PMID:22031863	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:268000	Retinitis pigmentosa		HP:0001133	OMIM:268000	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2019-07-03]
OMIM:268000	Retinitis pigmentosa		HP:0000662	OMIM:268000	IEA					P	HPO:iea[2009-02-17]
OMIM:268000	Retinitis pigmentosa		HP:0031605	OMIM:268000	TAS					P	HPO:nvasilevsky[2019-03-07];HPO:nvasilevsky[2019-03-07]
OMIM:268000	Retinitis pigmentosa		HP:0001419	OMIM:268000	TAS					I	HPO:nvasilevsky[2019-03-07];HPO:nvasilevsky[2019-03-07];HPO:probinson[2019-07-03]
OMIM:268000	Retinitis pigmentosa		HP:0000007	OMIM:268000	TAS					I	HPO:nvasilevsky[2019-03-07];HPO:nvasilevsky[2019-03-07];HPO:probinson[2019-07-03]
OMIM:268000	Retinitis pigmentosa		HP:0000510	OMIM:268000	TAS		20/20			P	HPO:nvasilevsky[2019-03-07];HPO:iea[2009-02-17]
OMIM:268000	Retinitis pigmentosa		HP:0000006	OMIM:268000	TAS					I	HPO:nvasilevsky[2019-03-07];HPO:nvasilevsky[2019-03-07];HPO:probinson[2019-07-03]
OMIM:605027	Lymphoma, non-hodgkin, familial		HP:0002665	OMIM:605027	IEA					P	HPO:skoehler[2013-01-09]
OMIM:225100	Ectopia lentis		HP:0000007	OMIM:225100	IEA					I	HPO:iea[2009-02-17]
OMIM:225100	Ectopia lentis		HP:0001083	OMIM:225100	IEA					P	HPO:iea[2009-02-17]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0034804	PMID:10192395	PCS					P	HPO:probinson[2023-07-18]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0011463	PMID:10192395	PCS					C	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-07]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0001131	PMID:10192395	PCS	HP:0011463				P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-07]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0000613	PMID:10192395	PCS	HP:0011463				P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-07]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0000007	PMID:10192395	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-07]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0007663	PMID:10192395	PCS	HP:0011462				P	HPO:skoehler[2015-07-26];HPO:probinson[2022-11-07]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0000505	PMID:10192395	PCS	HP:0011462				P	HPO:skoehler[2013-08-12];HPO:probinson[2022-11-07]
OMIM:204870	Corneal dystrophy, gelatinous drop-like		HP:0000622	PMID:10192395	PCS	HP:0011463				P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-07]
OMIM:608265	Deafness, congenital neurosensory, autosomal recessive 39		HP:0000007	OMIM:608265	TAS					I	HPO:probinson[2009-02-17]
OMIM:608265	Deafness, congenital neurosensory, autosomal recessive 39		HP:0000399	OMIM:608265	TAS					P	HPO:probinson[2009-02-17]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001771	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000286	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002421	PMID:29868776	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0010804	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002188	PMID:29868776	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0004322	PMID:29868776	PCS		8/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001250	PMID:29868776	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000160	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0025586	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001251	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002020	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0003593	PMID:29868776	PCS		8/8			C	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0032794	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0012469	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000316	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000954	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001803	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0007325	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001643	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001007	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001249	PMID:29868776	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0009748	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001601	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0005469	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001344	PMID:29868776	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000496	PMID:29868776	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0003487	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000298	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0011968	PMID:29868776	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000293	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002395	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001263	PMID:29868776	PCS		8/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0011800	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0006380	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002509	PMID:29868776	PCS		8/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000646	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000448	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000007	PMID:29868776	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002705	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000527	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000565	PMID:29868776	PCS		2/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001257	PMID:29868776	PCS		2/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000369	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001336	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001655	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002169	PMID:29868776	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002521	PMID:29868776	PCS		2/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000340	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000463	PMID:29868776	PCS		2/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000540	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0010665	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002080	PMID:29868776	PCS		2/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001508	PMID:29868776	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000737	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0012450	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0008551	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000657	PMID:29868776	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001347	PMID:29868776	PCS		3/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0008936	PMID:29868776	PCS		8/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002179	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000076	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002650	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001321	PMID:29868776	PCS		0/6			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002013	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0005484	PMID:29868776	PCS		7/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0034295	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0002205	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0000664	PMID:29868776	PCS		1/8			P	HPO:probinson[2023-02-07]
OMIM:618076	Neurodevelopmental disorder with spasticity and poor growth		HP:0001510	PMID:29868776	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:613123	Brugada syndrome 8		HP:0012251	PMID:19165230	PCS		1/1			P	HPO:probinson[2013-06-02];HP:probinson[2019-04-19]
OMIM:613123	Brugada syndrome 8		HP:0011712	PMID:19165230	PCS		1/1			P	HP:probinson[2019-04-19]
OMIM:613123	Brugada syndrome 8		HP:0004756	PMID:19165230	PCS		1/1			P	HPO:probinson[2013-06-02];HP:probinson[2019-04-19]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0010628	OMIM:256850	TAS					P	HPO:skoehler[2013-05-03]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0000486	PMID:20949505	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003376	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003693	OMIM:256850	TAS					P	HPO:probinson[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003593	PMID:20949505	PCS		1/1			C	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002460	OMIM:256850	TAS					P	HPO:probinson[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002062	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003390	OMIM:256850	IEA					P	HPO:probinson[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001270	PMID:20949505	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0000639	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0000613	PMID:20949505	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0007002	OMIM:256850	IEA					P	HPO:probinson[2012-03-12]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002936	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003701	OMIM:256850	TAS					P	HPO:skoehler[2013-05-03]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001763	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0000256	PMID:20949505	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001249	OMIM:256850	IEA		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001347	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002212	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003621	OMIM:256850	TAS					C	HPO:probinson[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0006956	PMID:20949505	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001762	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002650	OMIM:256850	TAS					P	HPO:skoehler[2013-05-03]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002013	PMID:20949505	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001761	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001260	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001284	PMID:20949505	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003380	OMIM:256850	TAS					P	HPO:skoehler[2013-05-03]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001317	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0000007	PMID:11062483	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0007256	OMIM:256850	TAS					P	HPO:skoehler[2015-01-04]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0001258	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0003677	OMIM:256850	IEA					C	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002522	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:256850	Giant axonal neuropathy 1, autosomal recessive		HP:0002600	OMIM:256850	IEA					P	HPO:iea[2009-02-17]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0002256	OMIM:221400	IEA					P	HPO:iea[2009-02-17]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0002630	OMIM:221400	IEA					P	HPO:iea[2009-02-17]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0000407	OMIM:221400	TAS					P	HPO:probinson[2012-09-20]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0003075	OMIM:221400	TAS					P	HPO:probinson[2012-09-20]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0009830	OMIM:221400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0000007	OMIM:221400	IEA					I	HPO:iea[2009-02-17]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0001649	OMIM:221400	IEA					P	HPO:iea[2009-02-17]
OMIM:221400	Deafness, nerve type, with mesenteric diverticula of small bowel andprogressive sensory neuropathy		HP:0005229	OMIM:221400	IEA					P	HPO:iea[2009-02-17]
OMIM:615552	Episodic pain syndrome, familial, 3		HP:0012332	OMIM:615552	TAS		HP:0040282			P	HPO:skoehler[2014-11-26]
OMIM:615552	Episodic pain syndrome, familial, 3		HP:0012531	PMID:24207120	PCS				HP:0025303	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-25]
OMIM:615552	Episodic pain syndrome, familial, 3		HP:0003593	PMID:24207120	PCS					C	HPO:probinson[2023-01-25];HPO:probinson[2023-01-25]
OMIM:615552	Episodic pain syndrome, familial, 3		HP:0000006	PMID:24207120	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-01-25]
OMIM:191390	Inflammatory bowel disease 11		HP:0002014	OMIM:191390	IEA					P	HPO:iea[2009-02-17]
OMIM:191390	Inflammatory bowel disease 11		HP:0002037	OMIM:191390	TAS					P	HPO:probinson[2009-02-17]
OMIM:191390	Inflammatory bowel disease 11		HP:0002573	OMIM:191390	IEA					P	HPO:iea[2009-02-17]
OMIM:191390	Inflammatory bowel disease 11		HP:0001426	OMIM:191390	IEA					I	HPO:iea[2009-02-17]
OMIM:191390	Inflammatory bowel disease 11		HP:0001824	OMIM:191390	IEA					P	HPO:iea[2009-02-17]
OMIM:191390	Inflammatory bowel disease 11		HP:0002027	OMIM:191390	IEA					P	HPO:iea[2009-02-17]
OMIM:246470	Leukemia, acute myelocytic, with polyposis coli and colon cancer		HP:0005227	OMIM:246470	IEA					P	HPO:iea[2009-02-17]
OMIM:246470	Leukemia, acute myelocytic, with polyposis coli and colon cancer		HP:0003003	OMIM:246470	TAS					P	HPO:skoehler[2015-01-21]
OMIM:246470	Leukemia, acute myelocytic, with polyposis coli and colon cancer		HP:0004808	OMIM:246470	IEA					P	HPO:iea[2009-02-17]
OMIM:246470	Leukemia, acute myelocytic, with polyposis coli and colon cancer		HP:0000007	OMIM:246470	IEA					I	HPO:iea[2009-02-17]
OMIM:246470	Leukemia, acute myelocytic, with polyposis coli and colon cancer		HP:0000119	OMIM:246470	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0002321	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0001250	PMID:22009145	PCS		HP:0040284			P	HP:probinson[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0003394	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0001251	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0003470	PMID:28003083	PCS		HP:0040284			P	HPO:skoehler[2010-06-20]
OMIM:263800	Gitelman syndrome		HP:0001508	PMID:28003083	PCS		HP:0040284			P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0002917	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0001949	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0000934	PMID:28003083	PCS					P	HP:probinson[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0002615	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0001324	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0001962	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0030083	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0002019	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0003127	OMIM:263800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:263800	Gitelman syndrome		HP:0000017	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0004756	PMID:22009145	PCS		HP:0040284			P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0003324	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0003621	OMIM:263800	IEA					C	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0003401	PMID:28003083	PCS					P	HP:probinson[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0005567	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0003201	PMID:22009145	PCS		HP:0040284			P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0002013	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0001281	PMID:28003083	PCS					P	HP:probinson[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0012378	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0002829	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0000848	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0001959	PMID:28003083	PCS					P	HPO:skoehler[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0000805	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0000007	PMID:22009145	PCS					I	HP:probinson[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0001954	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0001657	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0000128	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0002900	OMIM:263800	IEA					P	HPO:iea[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0000823	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0000103	PMID:28003083	PCS					P	HP:probinson[2009-02-17]
OMIM:263800	Gitelman syndrome		HP:0001510	PMID:28003083	PCS					P	HP:probinson[2018-05-13]
OMIM:263800	Gitelman syndrome		HP:0002027	PMID:22009145	PCS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:263800	Gitelman syndrome		HP:0000622	PMID:22009145	PCS		HP:0040284			P	HP:probinson[2018-05-13]
OMIM:214450	Griscelli syndrome, type 1		HP:0001250	PMID:19318926;OMIM:214450	PCS		12/12			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0002220	PMID:9207796	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0001010	PMID:9207796;PMID:19318926;PMID:12897212	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0001252	PMID:9207796;PMID:19318926	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0001263	PMID:9207796;PMID:19318926	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0003593	PMID:9207796	PCS		3/3			C	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0011110	PMID:12897212	PCS		1/2			P	HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0000007	PMID:9207796	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0001008	PMID:19318926;OMIM:214450	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0002218	PMID:9207796;PMID:19318926;PMID:12897212	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0002227	PMID:12897212	PCS		2/2			P	HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0004527	PMID:19318926;PMID:12897212	PCS		4/4			P	HPO:probinson[2022-06-25]
OMIM:214450	Griscelli syndrome, type 1		HP:0001249	OMIM:214450	IEA					P	HPO:iea[2009-02-17]
OMIM:214450	Griscelli syndrome, type 1		HP:0002226	PMID:12897212	PCS		2/2			P	HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:611907	Episodic ataxia, type 7		HP:0002321	OMIM:611907	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611907	Episodic ataxia, type 7		HP:0002131	OMIM:611907	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611907	Episodic ataxia, type 7		HP:0001260	OMIM:611907	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611907	Episodic ataxia, type 7		HP:0001324	OMIM:611907	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611907	Episodic ataxia, type 7		HP:0000006	OMIM:611907	IEA					I	HPO:skoehler[2010-06-19]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000750	PMID:36103875	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0002650	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000343	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000431	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0001250	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0001252	PMID:36103875	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0003593	PMID:36103875	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0040183	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0012427	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0001270	PMID:36103875	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000609	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000639	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000958	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000729	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000733	PMID:36103875	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0000007	PMID:36103875	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0004209	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0008404	PMID:36103875	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0007018	PMID:36103875	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620502	Neurodevelopmental disorder with language delay and variable cognitive abnormalities		HP:0001249	PMID:36103875	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0009937	PMID:30520571;PMID:29808498	PCS		3/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000286	PMID:29808498	PCS		1/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0010804	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002389	PMID:30520571;PMID:29808498	PCS		4/8			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002540	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001371	PMID:29808498	PCS		1/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002066	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0003196	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001252	PMID:30520571;PMID:29808498	PCS		9/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0032794	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000280	PMID:30520571;PMID:29808498	PCS		7/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0010761	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0012471	PMID:29808498	PCS		1/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001845	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000316	PMID:30520571;PMID:29808498	PCS		3/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0003623	PMID:30520571	PCS					C	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001265	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0005469	PMID:29808498	PCS		2/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001583	PMID:29808498	PCS		2/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000574	PMID:29808498	PCS		2/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000331	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002079	PMID:29808498	PCS		2/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002750	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0011968	PMID:30520571;PMID:29808498	PCS		7/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002033	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001260	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001263	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0010557	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0009891	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000007	PMID:29808498	PCS					I	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000648	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000768	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000565	PMID:30520571	PCS		4/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001612	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000446	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000369	PMID:30520571;PMID:29808498	PCS		6/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000341	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000582	PMID:29808498	PCS		1/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000343	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000463	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002240	PMID:30520571;PMID:29808498	PCS		2/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0012450	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002119	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0009765	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000218	PMID:30520571;PMID:29808498	PCS		5/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001320	PMID:29808498	PCS		3/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000431	PMID:29808498	PCS		2/3			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002650	PMID:30520571;PMID:29808498	PCS		3/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002098	PMID:30520571;PMID:29808498	PCS		6/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000270	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000592	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001284	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0011344	PMID:30520571	PCS		5/5			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0012510	PMID:30520571	PCS		2/5			P	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000506	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001639	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000348	PMID:30520571	PCS		4/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0002205	PMID:30520571;PMID:29808498	PCS		4/9			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001357	PMID:30520571	PCS		1/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0007018	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0001631	PMID:30520571	PCS		2/6			P	HPO:probinson[2021-07-14]
OMIM:619383	Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities		HP:0000545	PMID:29808498	PCS		1/3			P	HPO:probinson[2021-07-14]
OMIM:613876	Cardiomyopathy, familial hypertrophic, 20		HP:0003621	PMID:20970104	PCS		1/6			C	HPO:probinson[2022-07-04]
OMIM:613876	Cardiomyopathy, familial hypertrophic, 20		HP:0001639	PMID:20970104	PCS		6/6			P	HPO:probinson[2022-07-04]
OMIM:613876	Cardiomyopathy, familial hypertrophic, 20		HP:0003581	PMID:20970104	PCS		5/6			C	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:613876	Cardiomyopathy, familial hypertrophic, 20		HP:0005110	PMID:20970104	PCS		1/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-04]
OMIM:613876	Cardiomyopathy, familial hypertrophic, 20		HP:0001712	PMID:20970104	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613876	Cardiomyopathy, familial hypertrophic, 20		HP:0012664	PMID:20970104	PCS		0/6			P	HPO:probinson[2022-07-04]
OMIM:613876	Cardiomyopathy, familial hypertrophic, 20		HP:0000006	PMID:20970104	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613862	Retinitis pigmentosa 38		HP:0001133	PMID:11062461	PCS		2/2			P	HPO:probinson[2022-11-20]
OMIM:613862	Retinitis pigmentosa 38		HP:0000662	PMID:11062461	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-11-20]
OMIM:613862	Retinitis pigmentosa 38		HP:0200070	OMIM:613862	TAS					P	HPO:skoehler[2013-05-31]
OMIM:613862	Retinitis pigmentosa 38		HP:0000529	PMID:11062461	PCS		2/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-11-20]
OMIM:613862	Retinitis pigmentosa 38		HP:0011463	PMID:11062461	PCS		2/2			C	HPO:probinson[2022-11-20]
OMIM:613862	Retinitis pigmentosa 38		HP:0000007	PMID:11062461	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2022-11-20]
OMIM:613862	Retinitis pigmentosa 38		HP:0007401	OMIM:613862	TAS					P	HPO:skoehler[2015-07-26]
OMIM:613862	Retinitis pigmentosa 38		HP:0000543	OMIM:613862	TAS					P	HPO:skoehler[2013-05-31]
OMIM:613862	Retinitis pigmentosa 38		HP:0000510	PMID:11062461	PCS		2/2			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-11-20]
OMIM:222690	Dibasic amino aciduria I		HP:0003268	OMIM:222690	IEA					P	HPO:iea[2009-02-17]
OMIM:222690	Dibasic amino aciduria I		HP:0003532	OMIM:222690	IEA					P	HPO:iea[2009-02-17]
OMIM:222690	Dibasic amino aciduria I		HP:0002024	OMIM:222690	IEA					P	HPO:iea[2009-02-17]
OMIM:222690	Dibasic amino aciduria I		HP:0003168	OMIM:222690	IEA					P	HPO:iea[2009-02-17]
OMIM:222690	Dibasic amino aciduria I		HP:0003297	OMIM:222690	IEA					P	HPO:iea[2009-02-17]
OMIM:222690	Dibasic amino aciduria I		HP:0000007	OMIM:222690	IEA					I	HPO:iea[2009-02-17]
OMIM:222690	Dibasic amino aciduria I		HP:0001249	OMIM:222690	IEA					P	HPO:iea[2009-02-17]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0002300	PMID:36401616	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0000365	PMID:36401616	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001252	PMID:36401616	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001251	PMID:36401616	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0003593	PMID:36401616	PCS		2/3			C	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0010665	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001270	PMID:36401616	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0033725	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0000718	PMID:36401616	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0000752	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0003623	PMID:36401616	PCS		1/3			C	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0002254	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001321	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0011968	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0002451	PMID:36401616	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001263	PMID:36401616	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001639	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0000729	PMID:36401616	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0000668	PMID:36401616	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0000007	PMID:36401616	PCS					I	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001511	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0005616	PMID:36401616	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001337	PMID:36401616	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620270	Neurodevelopmental disorder with absent speech and movement and behavioral abnormalities		HP:0001513	PMID:36401616	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0000750	OMIM:300425	IEA		HP:0040282			P	HPO:skoehler[2010-06-20]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0002353	OMIM:300425	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-01]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0002332	OMIM:300425	IEA					P	HPO:iea[2009-02-17]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0001250	OMIM:300425	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0003144	OMIM:300425	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0011463	PMID:12669065	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0000717	PMID:12669065	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-01]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0000723	OMIM:300425	TAS					P	HPO:skoehler[2013-06-04]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0000733	OMIM:300425	TAS					P	HPO:probinson[2009-02-17]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0000758	OMIM:300425	IEA					P	HPO:iea[2009-02-17]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0001417	PMID:12669065	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0000732	OMIM:300425	IEA					P	HPO:iea[2009-02-17]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0001249	OMIM:300425	IEA					P	HPO:iea[2009-02-17]
OMIM:300425	Autism susceptibility, X-linked 1		HP:0000721	OMIM:300425	IEA					P	HPO:iea[2009-02-17]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000486	PMID:30057029	PCS		8/8			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0004322	PMID:30057029	PCS		4/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0004442	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0003196	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002020	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0010296	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0012471	PMID:30057029	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000915	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000637	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000752	PMID:30057029	PCS		3/10			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002019	PMID:30057029	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000358	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002553	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000494	PMID:30057029	PCS		5/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000252	PMID:30057029	PCS		5/20			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000098	PMID:30057029	PCS		2/20			P	HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000490	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001065	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0033454	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001182	PMID:30057029	PCS		1/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0011003	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000403	PMID:30057029	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000527	PMID:30057029	PCS		5/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000400	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001852	PMID:30057029	PCS		3/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000520	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000006	PMID:30057029	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000248	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000369	PMID:30057029	PCS		2/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000343	PMID:30057029	PCS		2/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000463	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000337	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000975	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000736	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000219	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0030084	PMID:30057029	PCS		3/20			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000218	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000455	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000179	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000457	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002236	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001166	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000750	PMID:30057029	PCS		20/20			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0004279	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002376	PMID:30057029	PCS		2/17			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000232	PMID:30057029	PCS		1/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002013	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002099	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000193	PMID:30057029	PCS		1/20			P	HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0003100	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0010812	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0011229	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000629	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000348	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002007	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0009836	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000347	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0004942	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000286	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0010804	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001770	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001773	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001250	PMID:30057029	PCS		6/20			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0003396	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000160	PMID:30057029	PCS		1/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001252	PMID:30057029	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0410030	PMID:30057029	PCS		1/20			P	HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000280	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0045075	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001090	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000319	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000316	PMID:30057029	PCS		3/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000954	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0020045	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001769	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001763	PMID:30057029	PCS		2/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000278	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001007	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001249	PMID:30057029	PCS		20/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000175	PMID:30057029	PCS		1/20			P	HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002750	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000293	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001382	PMID:30057029	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001263	PMID:30057029	PCS		20/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0031354	PMID:30057029	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000729	PMID:30057029	PCS		8/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0011330	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000448	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0005617	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002107	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000322	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000325	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0010749	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0004467	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000540	PMID:30057029	PCS		2/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002719	PMID:30057029	PCS		6/20			P	HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000938	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0008551	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000414	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001869	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002714	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001500	PMID:30057029	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000411	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0009921	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000256	PMID:30057029	PCS		2/20			P	HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000154	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000431	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0031936	PMID:30057029	PCS		11/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000276	PMID:30057029	PCS		2/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0045025	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0011271	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000426	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000307	PMID:30057029	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002967	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001357	OMIM:618089	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0002205	PMID:30057029	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0200055	PMID:30057029	PCS		2/20			P	HPO:skoehler[2018-10-08]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001631	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000028	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000303	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0001513	PMID:30057029	PCS		5/20			P	HPO:probinson[2022-11-09]
OMIM:618089	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities		HP:0000786	PMID:30057029	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0000750	PMID:19914906	PCS					P	HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0001250	PMID:19914906	PCS		5/16			P	HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0001263	PMID:19914906	PCS					P	HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0000316	PMID:19914906	PCS					P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0008872	PMID:19914906	PCS		8/16			P	HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0011800	PMID:19914906	PCS					P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0000337	PMID:19914906	PCS					P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0001270	PMID:19914906	PCS		8/16			P	HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0001466	PMID:19914906	PCS					I	HPO:probinson[2017-06-21];HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0000256	PMID:19914906	PCS					P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:611913	Chromosome 16p11.2 deletion syndrome, 593-kb		HP:0000347	PMID:19914906	PCS					P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:127750	Dementia, lewy body		HP:0002367	OMIM:127750	IEA					P	HPO:iea[2009-02-17]
OMIM:127750	Dementia, lewy body		HP:0100315	OMIM:127750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:127750	Dementia, lewy body		HP:0001300	OMIM:127750	IEA					P	HPO:iea[2009-02-17]
OMIM:127750	Dementia, lewy body		HP:0000726	OMIM:127750	IEA					P	HPO:iea[2009-02-17]
OMIM:127750	Dementia, lewy body		HP:0000746	OMIM:127750	IEA					P	HPO:iea[2009-02-17]
OMIM:127750	Dementia, lewy body		HP:0007159	OMIM:127750	IEA					P	HPO:iea[2009-02-17]
OMIM:127750	Dementia, lewy body		HP:0000006	OMIM:127750	IEA					I	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0011939	PMID:11478532	PCS		1/8			P	HPO:probinson[2024-07-22]
OMIM:107480	Townes-Brocks syndrome 1		HP:0002025	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001177	OMIM:107480;PMID:11478532	PCS		11/18			P	HPO:probinson[2022-03-28];HPO:skoehler[2012-10-12]
OMIM:107480	Townes-Brocks syndrome 1		HP:0002023	PMID:9425907;PMID:22308078	PCS		105/158			P	HPO:probinson[2022-03-28];HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0002144	PMID:11478532	PCS		2/8			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000089	PMID:11478532	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000083	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0002020	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0010331	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000238	PMID:11478532	PCS		1/8			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0009944	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001249	OMIM:107480	IEA					P	HPO:skoehler[2019-04-18]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000252	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000453	PMID:11478532	PCS		1/8			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0004453	OMIM:107480	PCS					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001263	PMID:22308078	PCS		23/89			P	HPO:iea[2018-03-12]
OMIM:107480	Townes-Brocks syndrome 1		HP:0004692	PMID:11478532	PCS		1/8			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0004691	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0010711	PMID:11478532	PCS		1/8			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0010481	OMIM:107480	IEA					P	HPO:skoehler[2010-06-20]
OMIM:107480	Townes-Brocks syndrome 1		HP:0100015	OMIM:107480	IEA					P	HPO:skoehler[2010-06-18]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000407	PMID:9425907;PMID:9973281	PCS		17/21			P	HPO:probinson[2022-03-28];HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001537	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0009779	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000048	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000400	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000047	PMID:9973281	PCS		3/17			P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000003	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000006	PMID:9425907	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000567	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000143	PMID:9425907	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001199	PMID:9425907;PMID:9973281	PCS		9/21			P	HPO:probinson[2022-03-28];HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0003577	PMID:9425907	PCS		4/4			C	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0004467	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000384	OMIM:107480;PMID:9425907	PCS		13/14			P	HPO:probinson[2022-03-28];HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0030676	PMID:3180506	PCS					P	HPO:skoehler[2015-12-30]
OMIM:107480	Townes-Brocks syndrome 1		HP:0010743	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001629	PMID:11478532;PMID:9973281	PCS		3/25			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28];HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0008551	PMID:9425907	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0006179	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000136	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0009921	OMIM:107480	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001864	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000110	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0002575	PMID:11478532	PCS		1/8			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001440	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000076	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001883	PMID:11478532	PCS		1/8			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001360	PMID:11478532	PCS		1/8			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000394	PMID:9425907	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0004792	PMID:9425907	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0011304	PMID:9425907	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001518	PMID:9425907	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001636	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000821	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0001631	PMID:9425907	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:107480	Townes-Brocks syndrome 1		HP:0000028	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:107480	Townes-Brocks syndrome 1		HP:0002247	OMIM:107480	IEA					P	HPO:iea[2009-02-17]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000494	PMID:27049303	PCS					P	HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000431	PMID:27049303	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0002299	PMID:27049303	PCS		56/56			P	HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000968	PMID:27049303	PCS		11/56			P	HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0012471	PMID:27049303	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000294	PMID:27049303	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000316	PMID:27049303	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000007	PMID:27049303	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000653	PMID:27049303	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0005280	PMID:27049303	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0045074	PMID:27049303	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617392	Ectodermal dysplasia 13, Hair/tooth type		HP:0000677	PMID:27049303	PCS		56/56			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0031318	PMID:33974137	PCS		3/7			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0003687	PMID:33974137	PCS		3/7			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0003596	PMID:33974137	PCS		7/10			C	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0000365	PMID:33974137	PCS		0/10			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0008959	PMID:33974137	PCS		7/10			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0003691	PMID:33974137	PCS		5/10			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0012548	PMID:33974137	PCS		7/8			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0100303	PMID:33974137	PCS		4/7			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0009053	PMID:33974137	PCS		10/10			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0000518	PMID:33974137	PCS		0/10			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0001419	PMID:33974137	PCS					I	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0011462	PMID:33974137	PCS		3/10			C	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0003805	PMID:33974137	PCS		5/7			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0001638	PMID:33974137	PCS		0/9			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0002747	PMID:33974137	PCS		0/10			P	HPO:probinson[2022-06-13]
OMIM:301075	Myopathy, distal, 7, adult-onset, X-linked		HP:0003557	PMID:33974137	PCS		5/7			P	HPO:probinson[2022-06-13]
OMIM:122600	Spondylocostal dysostosis 5		HP:0003510	OMIM:122600	TAS					P	HPO:skoehler[2015-02-22]
OMIM:122600	Spondylocostal dysostosis 5		HP:0003521	PMID:23335591	PCS		3/3			P	HPO:probinson[2015-02-21];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0003577	PMID:25564734	PCS		23/23			C	HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0002650	PMID:23335591	PCS		3/3			P	HPO:probinson[2015-02-21];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0002650	PMID:25564734	PCS	HP:0003577	23/23			P	HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0003396	PMID:25564734	PCS		1/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0000470	OMIM:122600	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:122600	Spondylocostal dysostosis 5		HP:0000913	OMIM:122600	TAS					P	HPO:probinson[2009-02-17]
OMIM:122600	Spondylocostal dysostosis 5		HP:0002937	PMID:25564734;PMID:23335591	PCS		26/26			P	HPO:probinson[2022-08-03];HPO:probinson[2009-02-17];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0002948	PMID:23335591	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0003419	OMIM:122600	TAS					P	HPO:skoehler[2010-06-20]
OMIM:122600	Spondylocostal dysostosis 5		HP:0000921	PMID:25564734	PCS		15/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0000007	PMID:25564734	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0005815	OMIM:122600	TAS					P	HPO:skoehler[2017-07-13]
OMIM:122600	Spondylocostal dysostosis 5		HP:0000768	OMIM:122600	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:122600	Spondylocostal dysostosis 5		HP:0003316	PMID:25564734	PCS		5/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-03]
OMIM:122600	Spondylocostal dysostosis 5		HP:0000006	PMID:23335591	PCS					I	HPO:probinson[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000343	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0002980	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0004443	OMIM:207410	IEA					P	HPO:iea[2012-02-24]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000260	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0001371	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0003275	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0002781	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0003031	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0004440	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000063	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0012210	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000238	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000059	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000774	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000377	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0001249	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0001166	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000453	OMIM:207410	TAS					P	HPO:probinson[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000452	OMIM:207410	TAS					P	HPO:skoehler[2013-06-12]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000272	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0003041	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0011800	OMIM:207410	TAS					P	HPO:skoehler[2013-11-28]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0005280	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0012385	OMIM:207410	TAS					P	HPO:skoehler[2013-10-22]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0001838	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0002007	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000520	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0001631	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000248	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000402	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000006	OMIM:207410	TAS					I	HPO:skoehler[2019-04-18]
OMIM:207410	Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis		HP:0000148	OMIM:207410	IEA					P	HPO:iea[2009-02-17]
OMIM:609812	Maturity-Onset diabetes of the young, type 8, with exocrine dysfunction		HP:0001738	PMID:16369531	PCS					P	HPO:probinson[2023-03-08]
OMIM:609812	Maturity-Onset diabetes of the young, type 8, with exocrine dysfunction		HP:0011462	PMID:16369531	PCS					C	HPO:probinson[2023-03-08]
OMIM:609812	Maturity-Onset diabetes of the young, type 8, with exocrine dysfunction		HP:0004904	PMID:16369531	PCS					P	HPO:probinson[2013-03-31];HPO:probinson[2023-03-08]
OMIM:609812	Maturity-Onset diabetes of the young, type 8, with exocrine dysfunction		HP:0003074	PMID:16369531	PCS					P	HPO:probinson[2023-03-08]
OMIM:609812	Maturity-Onset diabetes of the young, type 8, with exocrine dysfunction		HP:0040217	PMID:16369531	PCS					P	HPO:probinson[2023-03-08]
OMIM:609812	Maturity-Onset diabetes of the young, type 8, with exocrine dysfunction		HP:0000006	PMID:16369531	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-03-08]
OMIM:609812	Maturity-Onset diabetes of the young, type 8, with exocrine dysfunction		HP:0002027	PMID:16369531	PCS					P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-08]
OMIM:126300	DISTICHIASIS		HP:0009743	OMIM:126300	IEA					P	HPO:iea[2009-02-17]
OMIM:126300	DISTICHIASIS		HP:0000006	OMIM:126300	IEA					I	HPO:iea[2009-02-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001771	PMID:22541562	PCS		2/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0003236	PMID:22541559	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000365	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000486	PMID:22541562;PMID:22541559	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0004322	PMID:22541562;PMID:22541559	PCS		8/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001250	PMID:22541562;PMID:36420349;PMID:22541559	PCS		2/15			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-06-18];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0002066	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001252	PMID:22541559	PCS		9/11			P	HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0003593	PMID:22541562	PCS		3/3			C	HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0002064	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0011463	PMID:36420349	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000319	PMID:22541559	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000717	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000316	OMIM:611091	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0008897	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001249	PMID:36420349;PMID:22541559	PCS		12/12			P	HPO:skoehler[2013-06-16];HPO:probinson[2022-06-18];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000252	PMID:36420349;PMID:22541559	PCS		9/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001344	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000574	PMID:22541559	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000331	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001260	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001263	PMID:36420349;OMIM:611091	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-07-14];HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0004692	PMID:22541562	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0033454	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000448	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000007	PMID:22541559	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000964	OMIM:611091	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000601	PMID:22541559	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000322	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001257	OMIM:611091	TAS	HP:0003584				P	HPO:skoehler[2012-11-28]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000049	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001276	PMID:22541562;PMID:22541559	PCS		11/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000581	OMIM:611091	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0008070	OMIM:611091	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0025435	PMID:22541562	PCS		2/2			P	HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000215	PMID:22541559	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001347	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0008936	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000275	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0002136	PMID:22541562	PCS		2/3			P	HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000750	OMIM:611091	TAS					P	HPO:skoehler[2014-11-26]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000431	OMIM:611091	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000276	PMID:22541559	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001761	PMID:22541562	PCS		2/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000430	PMID:22541559	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0003186	PMID:36420349	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0001518	OMIM:611091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000506	OMIM:611091	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000426	OMIM:611091	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000664	PMID:22541559	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-18]
OMIM:611091	Intellectual developmental disorder, autosomal recessive 5		HP:0000666	PMID:22541562	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0008715	PMID:34452636	PCS		3/3			P	HPO:probinson[2021-09-24]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0003487	PMID:17480217	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0001250	OMIM:300419	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0001252	PMID:17480217	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0000020	PMID:17480217	PCS		2/4			P	HPO:probinson[2021-09-24]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0001419	PMID:11971879	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2019-09-07]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0000407	PMID:17480217	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0000629	OMIM:300419	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0000637	OMIM:300419	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0002307	PMID:17480217	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0001763	PMID:17480217	PCS		3/4			P	HPO:probinson[2021-09-24]
OMIM:300419	Intellectual developmental disorder, X-linked 29		HP:0001249	PMID:11971879;PMID:17480217	PCS		14/14			P	HPO:probinson[2013-02-17];HPO:probinson[2019-09-07];HPO:probinson[2021-09-24]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0002025	PMID:18775957	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0003577	PMID:18775957;PMID:20087400	PCS		3/3			C	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0025660	PMID:18775957	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0001696	OMIM:613686	TAS					P	HPO:skoehler[2014-01-28]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0003310	OMIM:613686	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0004322	PMID:18775957;PMID:20087400	PCS		2/3			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0001651	OMIM:613686	TAS					P	HPO:skoehler[2014-01-28]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0001591	PMID:18775957	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0003298	PMID:20087400	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0010306	PMID:18775957	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0032341	PMID:20087400	PCS		1/1			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0002937	PMID:20087400	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0032342	PMID:20087400	PCS		1/1			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000238	PMID:18775957	PCS	HP:0034197	1/1			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0003305	OMIM:613686	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0003422	PMID:18775957;PMID:20087400	PCS		3/3			P	HPO:probinson[2023-02-10];HPO:probinson[2015-02-21];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000011	PMID:18775957	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0002650	PMID:20087400	PCS		1/2			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000475	PMID:20087400	PCS		1/2			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0030323	OMIM:613686	TAS					P	HPO:probinson[2015-04-19]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0002475	PMID:18775957	PCS		1/1			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0030322	PMID:20087400	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0004397	PMID:18775957	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000470	PMID:20087400	PCS		1/2			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0034566	PMID:20087400	PCS		2/2			P	HPO:probinson[2023-03-31]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0002091	PMID:20087400	PCS		1/1			P	HPO:probinson[2015-02-21];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000902	PMID:18775957;PMID:20087400	PCS		2/3			P	HPO:probinson[2023-02-10];HPO:probinson[2015-02-21];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0002948	PMID:18775957	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000767	PMID:20087400	PCS		1/2			P	HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000921	PMID:20087400	PCS		1/2			P	HPO:probinson[2015-02-21];HPO:probinson[2023-02-10]
OMIM:613686	Spondylocostal dysostosis 4, autosomal recessive		HP:0000007	PMID:18775957	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:303110	Xq21 deletion syndrome		HP:0001133	OMIM:303110	IEA					P	HPO:iea[2009-02-17]
OMIM:303110	Xq21 deletion syndrome		HP:0000365	PMID:3476958;PMID:20412083	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-27];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0000662	PMID:18487380	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0001263	PMID:20412083	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0000408	OMIM:303110	TAS					P	HPO:skoehler[2012-10-17]
OMIM:303110	Xq21 deletion syndrome		HP:0000529	OMIM:303110	IEA					P	HPO:iea[2009-02-17]
OMIM:303110	Xq21 deletion syndrome		HP:0001419	PMID:20412083	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0011373	PMID:20412083	PCS		2/2			P	HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0000405	PMID:20412083	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0200065	OMIM:303110	TAS					P	HPO:probinson[2009-02-17]
OMIM:303110	Xq21 deletion syndrome		HP:0001466	PMID:20412083	PCS					I	HPO:skoehler[2013-01-22];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0001139	PMID:3476958;PMID:18487380	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-27];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0001249	PMID:3476958	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-27]
OMIM:303110	Xq21 deletion syndrome		HP:0001513	OMIM:303110	IEA					P	HPO:iea[2009-02-17]
OMIM:303110	Xq21 deletion syndrome		HP:0000533	OMIM:303110	TAS					P	HPO:probinson[2009-02-17]
OMIM:258100	Oguchi disease 1		HP:0000007	PMID:7670478	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:258100	Oguchi disease 1		HP:0007642	PMID:7670478	PCS		6/6			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-22]
OMIM:258100	Oguchi disease 1		HP:0030824	PMID:7670478	PCS		6/6			P	HPO:probinson[2023-02-22]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001254	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0003577	PMID:22922874	PCS		1/2			C	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0000023	PMID:22922874	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001591	PMID:22922874	PCS		1/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001252	PMID:22922874	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002020	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002160	PMID:22922874	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0033443	PMID:22922874	PCS		1/1			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001508	PMID:22922874	PCS		2/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0000316	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002912	PMID:22922874	PCS		1/1			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0025116	PMID:22922874	PCS		1/3			P	HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0006610	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001643	PMID:22922874	PCS		1/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002533	PMID:22922874	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0003623	PMID:22922874	PCS		1/2			C	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0003524	OMIM:614857	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002059	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0003145	OMIM:614857	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002156	PMID:22922874	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002750	PMID:22922874	PCS		1/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0003223	OMIM:614857	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0011968	PMID:22922874	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001263	PMID:22922874	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001680	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002092	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0012120	PMID:22922874	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0000888	PMID:22922874	PCS		1/3			P	HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0000007	PMID:22922874	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001873	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0002789	PMID:22922874	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001895	PMID:22922874	PCS		2/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0003658	PMID:22922874	PCS		1/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001510	PMID:22922874	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001631	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0000347	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0000028	PMID:22922874	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:614857	Methylmalonic aciduria and homocystinuria, Cblj type		HP:0001875	PMID:22922874	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-06]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0002015	OMIM:211500	IEA					P	HPO:iea[2009-02-17]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0005951	OMIM:211500	IEA					P	HPO:iea[2009-02-17]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0001283	OMIM:211500	IEA					P	HPO:iea[2009-02-17]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0009113	OMIM:211500	IEA					P	HPO:iea[2009-02-17]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0000508	OMIM:211500	IEA					P	HPO:iea[2009-02-17]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0007034	OMIM:211500	IEA					P	HPO:iea[2009-02-17]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0000007	OMIM:211500	IEA					I	HPO:iea[2009-02-17]
OMIM:211500	Bulbar palsy, progressive, of childhood		HP:0001349	OMIM:211500	IEA					P	HPO:iea[2009-02-17]
OMIM:615591	Macular degeneration, age-related, 15, susceptibility to		HP:0000608	PMID:32246154	PCS					P	HPO:probinson[2022-08-10]
OMIM:615591	Macular degeneration, age-related, 15, susceptibility to		HP:0003581	PMID:32246154	PCS					C	HPO:probinson[2022-08-10]
OMIM:615591	Macular degeneration, age-related, 15, susceptibility to		HP:0000006	PMID:32246154	PCS					I	HPO:probinson[2022-08-10]
OMIM:616098	Immunodeficiency 37		HP:0004313	PMID:25365219	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0002133	PMID:25365219	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0410388	PMID:25365219	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0001250	PMID:25365219	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0002719	PMID:25365219	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0002583	PMID:25365219	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0002383	PMID:25365219	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0003593	PMID:25365219	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0000007	PMID:25365219	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-30]
OMIM:616098	Immunodeficiency 37		HP:0002721	PMID:25365219	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-30]
OMIM:616517	Achromatopsia 7		HP:0000639	PMID:26029869	PCS		4/6			P	HPO:probinson[2018-03-07]
OMIM:616517	Achromatopsia 7		HP:0007750	PMID:26029869	PCS		5/6			P	HPO:probinson[2018-03-07]
OMIM:616517	Achromatopsia 7		HP:0000613	PMID:26029869	PCS		5/6			P	HPO:probinson[2016-05-30]
OMIM:616517	Achromatopsia 7		HP:0007663	PMID:26029869	PCS		6/6			P	HPO:probinson[2018-03-07]
OMIM:616517	Achromatopsia 7		HP:0000007	PMID:26029869	PCS					I	HPO:probinson[2018-03-07]
OMIM:616517	Achromatopsia 7		HP:0000603	PMID:26029869	PCS		2/6			P	HPO:probinson[2018-03-07]
OMIM:616517	Achromatopsia 7		HP:0007401	PMID:26029869	PCS		5/6			P	HPO:probinson[2016-05-30]
OMIM:616517	Achromatopsia 7		HP:0011516	PMID:26029869	PCS		5/6			P	HPO:probinson[2018-03-07]
OMIM:616517	Achromatopsia 7		HP:0030825	PMID:26063662	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-10]
OMIM:108200	Arthrogryposis-Like hand anomaly and sensorineural deafness		HP:0005612	OMIM:108200	IEA					P	HPO:iea[2009-02-17]
OMIM:108200	Arthrogryposis-Like hand anomaly and sensorineural deafness		HP:0000407	OMIM:108200	IEA					P	HPO:iea[2009-02-17]
OMIM:108200	Arthrogryposis-Like hand anomaly and sensorineural deafness		HP:0002804	OMIM:108200	IEA					P	HPO:skoehler[2015-01-19]
OMIM:108200	Arthrogryposis-Like hand anomaly and sensorineural deafness		HP:0000006	OMIM:108200	IEA					I	HPO:iea[2009-02-17]
OMIM:617609	Nephrotic syndrome, type 15		HP:0003774	PMID:27932480	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617609	Nephrotic syndrome, type 15		HP:0003593	PMID:27932480	PCS		3/3			C	HPO:probinson[2023-02-10]
OMIM:617609	Nephrotic syndrome, type 15		HP:0003073	PMID:27932480	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617609	Nephrotic syndrome, type 15		HP:0000007	PMID:27932480	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:617609	Nephrotic syndrome, type 15		HP:0000093	PMID:27932480	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617609	Nephrotic syndrome, type 15		HP:0012588	PMID:27932480	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:617609	Nephrotic syndrome, type 15		HP:0012579	PMID:27932480	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001397	PMID:21963049	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0003235	PMID:21963049	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0002465	PMID:21963049	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001396	PMID:21963049	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0003676	PMID:21963049	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0003236	PMID:21963049	PCS		3/6			P	HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001250	PMID:21963049	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001252	PMID:21963049	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0003593	OMIM:614300	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0010841	PMID:21963049	PCS		2/2			P	HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0034731	PMID:21963049	PCS		6/6			P	HPO:probinson[2023-06-05]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0034730	PMID:21963049	PCS		5/6			P	HPO:probinson[2023-06-05]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0031964	PMID:21963049	PCS		6/6			P	HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0008151	PMID:21963049	PCS		4/5			P	HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001508	PMID:21963049	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0000316	PMID:21963049	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001786	OMIM:614300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001324	PMID:21963049	PCS		2/2			P	HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0000256	PMID:21963049	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001642	PMID:21963049	PCS		1/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0003623	PMID:21963049	PCS		2/2			C	HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0003202	PMID:21963049	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0002059	PMID:21963049	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0000750	PMID:21963049	PCS		2/2			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001684	PMID:21963049	PCS		2/6			P	HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0001680	PMID:21963049	PCS		1/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0012736	PMID:21963049	PCS		2/6			P	HPO:probinson[2022-11-25];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0011344	PMID:21963049	PCS		4/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0006580	PMID:21963049	PCS		1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0000407	PMID:21963049	PCS		2/6			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0002904	PMID:21963049	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0000007	PMID:21963049	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0002007	PMID:21963049	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:614300	Hypermethioninemia due to adenosine kinase deficiency		HP:0500210	PMID:21963049	PCS		2/2			P	HPO:probinson[2022-11-25]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0007957	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000343	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000463	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0012368	OMIM:602562	TAS					P	HPO:skoehler[2013-10-22]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000319	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0008551	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000316	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000239	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000656	OMIM:602562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000637	OMIM:602562	TAS					P	HPO:skoehler[2013-05-29]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0003745	OMIM:602562	TAS					I	HPO:skoehler[2015-12-30]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000311	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000358	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000677	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0001028	OMIM:602562	IEA					P	HPO:skoehler[2019-09-07]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000154	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000494	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000431	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000574	OMIM:602562	TAS					P	HPO:skoehler[2013-05-31]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000491	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0005321	OMIM:602562	IEA					P	HPO:skoehler[2015-01-27]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000509	OMIM:602562	TAS					P	HPO:skoehler[2013-05-31]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000403	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000664	OMIM:602562	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:602562	Mandibulofacial dysostosis with macroblepharon and macrostomia		HP:0000347	OMIM:602562	TAS					P	HPO:skoehler[2013-05-21]
OMIM:145300	Hypersensitivity pneumonitis, familial		HP:0006516	OMIM:145300	IEA					P	HPO:iea[2009-02-17]
OMIM:145300	Hypersensitivity pneumonitis, familial		HP:0000006	OMIM:145300	IEA					I	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0001177	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0008606	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000164	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000486	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000365	PMID:18423521	PCS		5/6			P	HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0001057	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002021	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000480	PMID:18423521	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0001250	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002020	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0010566	OMIM:113620	IEA					P	HPO:skoehler[2010-06-20]
OMIM:113620	Branchiooculofacial syndrome		HP:0000518	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000639	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0001804	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000316	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000954	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0003307	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0008897	PMID:18423521	PCS		2/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0009623	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002216	PMID:18423521	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0002335	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000358	OMIM:113620	TAS					P	HPO:iea[2015-03-21]
OMIM:113620	Branchiooculofacial syndrome		HP:0000175	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000252	OMIM:113620	TAS					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0004334	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0010517	OMIM:113620	TAS					P	HPO:iea[2015-03-21]
OMIM:113620	Branchiooculofacial syndrome		HP:0010751	PMID:18423521	PCS		2/6			P	HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0011323	PMID:18423521	PCS		1/6			P	HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0000528	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000407	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000568	PMID:18423521	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0004209	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000405	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002987	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000047	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0009778	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000006	PMID:18423521	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0000204	OMIM:113620	IEA					P	HPO:skoehler[2010-06-20]
OMIM:113620	Branchiooculofacial syndrome		HP:0000369	OMIM:113620	TAS					P	HPO:skoehler[2015-04-05]
OMIM:113620	Branchiooculofacial syndrome		HP:0001611	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0004467	PMID:18423521	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0000582	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0010628	PMID:18423521	PCS		1/6			P	HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0004785	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000420	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0025247	OMIM:113620	IEA					P	HPO:skoehler[2018-10-08]
OMIM:113620	Branchiooculofacial syndrome		HP:0004464	OMIM:113620	TAS					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002162	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0005473	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0008070	PMID:18423521	PCS		1/6			P	HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0008551	OMIM:113620	TAS					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000612	PMID:18423521	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0000579	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000455	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0006610	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002558	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0008559	OMIM:113620	TAS					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000396	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002211	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000196	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000350	OMIM:113620	TAS					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000272	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000470	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0005280	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0002808	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000506	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0009794	OMIM:113620	TAS					P	HPO:skoehler[2012-10-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000508	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000987	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000107	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000268	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0001511	PMID:18423521	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-19]
OMIM:113620	Branchiooculofacial syndrome		HP:0000028	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000347	OMIM:113620	TAS					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000545	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:113620	Branchiooculofacial syndrome		HP:0000104	OMIM:113620	IEA					P	HPO:iea[2009-02-17]
OMIM:142309	Hemoglobin-Variants for which the chain carrying the mutation isunknown or uncertain		HP:0004863	OMIM:142309	TAS					P	HPO:probinson[2009-02-17]
OMIM:142309	Hemoglobin-Variants for which the chain carrying the mutation isunknown or uncertain		HP:0004825	OMIM:142309	IEA					P	HPO:iea[2009-02-17]
OMIM:142309	Hemoglobin-Variants for which the chain carrying the mutation isunknown or uncertain		HP:0000006	OMIM:142309	IEA					I	HPO:iea[2009-02-17]
OMIM:613309	Diamond-blackfan anemia 10		HP:0003577	PMID:23812780	PCS		2/4			C	HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000365	PMID:23812780	PCS		2/4			P	HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0004322	PMID:23812780	PCS		2/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000086	PMID:23812780;OMIM:613309	PCS		3/14			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0003593	PMID:20116044	PCS		4/4			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0033074	PMID:20116044	IEA		3/8			P	HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0001629	PMID:23812780	PCS		2/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0001903	PMID:20116044	PCS		8/8			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-blackfan anemia 10		HP:0011463	PMID:23812780	PCS		2/4			C	HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0008551	PMID:23812780	PCS		2/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0001643	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000413	PMID:23812780	PCS		2/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000776	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000358	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000175	PMID:23812780	PCS		2/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000475	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000453	PMID:23812780	PCS		1/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0002098	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0005321	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000075	PMID:23812780	PCS		1/4			P	HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000272	PMID:23812780	PCS		2/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0025194	PMID:23812780	PCS		1/4			P	HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000405	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0005815	PMID:23812780	PCS		1/4			P	HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0001896	OMIM:613309	TAS					P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0001510	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0001972	PMID:23812780	PCS		4/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000006	PMID:20116044	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-13]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000369	OMIM:613309	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613309	Diamond-Blackfan anemia 10		HP:0000347	PMID:23812780	PCS		1/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-13]
OMIM:188400	Digeorge syndrome		HP:0000122	PMID:16208694	PCS	HP:0003577	5/78			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0004322	PMID:16208694	PCS		16/78			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0010769	PMID:16208694	PCS		5/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001250	PMID:16208694	PCS		31/78			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001051	PMID:16208694	PCS		27/78			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000083	PMID:16208694	PCS		8/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0002020	PMID:16208694	PCS		6/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0012745	OMIM:188400	TAS					P	HPO:skoehler[2014-03-24]
OMIM:188400	Digeorge syndrome		HP:0011611	OMIM:188400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:188400	Digeorge syndrome		HP:0008211	PMID:28740581	PCS					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-25]
OMIM:188400	Digeorge syndrome		HP:0001328	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000316	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0020046	OMIM:188400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:188400	Digeorge syndrome		HP:0006510	PMID:16208694	PCS		6/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001643	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001249	PMID:16208694	PCS		72/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001660	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000175	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000252	PMID:16208694	PCS		5/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000370	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001263	OMIM:188400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:188400	Digeorge syndrome		HP:0001061	OMIM:188400	TAS		18/78			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0100541	OMIM:188400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:188400	Digeorge syndrome		HP:0011840	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001537	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0002627	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000646	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0002705	OMIM:188400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:188400	Digeorge syndrome		HP:0000403	PMID:16208694	PCS		27/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000647	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0002901	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0002307	PMID:16208694	PCS		5/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000565	OMIM:188400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:188400	Digeorge syndrome		HP:0000322	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000369	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000006	OMIM:188400	IEA					I	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001611	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000126	OMIM:188400;PMID:16208694	PCS		16/88			P	HPO:probinson[2022-03-17];HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001397	PMID:16208694	PCS		5/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000860	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000023	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000581	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0100750	PMID:16208694	PCS		16/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001629	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0002719	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001903	PMID:16208694	PCS		9/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000778	PMID:16208694	PCS		8/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000777	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0002999	PMID:16208694	PCS		9/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000218	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0007302	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0006532	PMID:16208694	PCS		30/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001269	PMID:16208694	PCS		5/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001744	PMID:16208694	PCS		8/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000138	PMID:16208694	PCS		7/42			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000577	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000110	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0008419	PMID:16208694	PCS		6/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0002650	PMID:16208694	PCS		37/78			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000750	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000034	PMID:16208694	PCS		5/36			P	HPO:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0025312	OMIM:188400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:188400	Digeorge syndrome		HP:0031817	PMID:28740581	PCS					P	HPO:lccarmody[2018-09-25]
OMIM:188400	Digeorge syndrome		HP:0000193	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0002099	PMID:16208694	PCS		10/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001081	PMID:16208694	PCS		15/78			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001281	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0011108	PMID:16208694	PCS		9/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0100753	PMID:16208694	PCS		7/31			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000627	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001636	OMIM:188400	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0000821	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0007018	OMIM:188400	IEA					P	HPO:iea[2009-02-17]
OMIM:188400	Digeorge syndrome		HP:0001873	PMID:16208694	PCS		22/78			P	HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0001513	PMID:16208694	PCS		27/78			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:188400	Digeorge syndrome		HP:0000347	PMID:28740581	IEA					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-25]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0001278	OMIM:610600	IEA					P	HPO:iea[2009-02-17]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0002153	PMID:9625333	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0000848	OMIM:610600	IEA					P	HPO:iea[2009-02-17]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0001508	PMID:9625333	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0032362	PMID:1594605	PCS		1/1			P	HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0001944	OMIM:610600	IEA					P	HPO:iea[2009-02-17]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0002902	PMID:9625333	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0020200	PMID:1594605	PCS		1/1			P	HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0000007	PMID:1594605	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0004319	PMID:9625333	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0001510	PMID:9625333	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0000127	PMID:9625333	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-15]
OMIM:610600	Hypoaldosteronism, congenital, due to CMO II deficiency		HP:0003623	OMIM:610600	IEA					C	HPO:iea[2009-02-17]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0033606	PMID:25597511	PCS		1/1			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001892	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0003676	PMID:25597510	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001332	PMID:25597511;PMID:25597510	PCS		4/18			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001250	PMID:25597511;PMID:25597510	PCS		6/19			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001371	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001252	PMID:25597510	PCS	HP:0003623	8/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001252	PMID:25597511	PCS		3/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001251	PMID:25597510	PCS		3/13			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0003593	PMID:25597511	IEA		4/5			C	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0010920	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000639	PMID:25597510	PCS		2/14			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000518	PMID:25597511;PMID:25597510	PCS		7/15			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0011461	PMID:25597511	PCS		1/5			C	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001249	PMID:25597510	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000252	PMID:25597511;PMID:25597510	PCS		10/19			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000211	PMID:25597510	PCS		1/14			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001266	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0011968	PMID:25597510	PCS		5/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001260	PMID:25597510	PCS		1/13			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002151	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001263	PMID:25597511;PMID:25597510	PCS		15/15			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0033454	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000007	PMID:25597510	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001257	PMID:25597510	PCS		4/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001337	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001336	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002487	PMID:25597510	PCS		1/13			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001397	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0003577	OMIM:616271	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0008905	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001272	PMID:25597510	PCS		7/8			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0033229	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0008151	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002719	PMID:25597511;PMID:25597510	PCS		6/19			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001944	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000414	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0006532	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001347	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002179	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001561	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002059	PMID:25597511;PMID:25597510	PCS		8/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001882	PMID:25597511	PCS		2/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002376	PMID:25597511	PCS		1/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002098	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0002490	PMID:25597511	PCS		1/1			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000629	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001998	PMID:25597510	PCS	HP:0003623	4/14			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001558	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001635	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001319	PMID:25597510	PCS		8/14			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001511	PMID:25597510	PCS		3/14			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001873	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001510	PMID:25597511	PCS		2/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0000347	PMID:25597511	PCS		1/5			P	HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0001875	PMID:25597511;PMID:25597510	PCS		14/19			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:616271	3-Methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia		HP:0003535	PMID:25597511;PMID:25597510	PCS		17/17			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0009826	PMID:33058759	PCS		5/6			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0003577	PMID:33058759	PCS					C	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0001674	PMID:33058759	PCS	HP:0003577				P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0000276	PMID:33058759	PCS		1/2			P	HPO:probinson[2021-01-16];HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0002164	PMID:33058759	PCS		3/5			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0011800	PMID:33058759	PCS		1/2			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0011833	PMID:33058759	PCS		1/2			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0000191	PMID:33058759	PCS		2/2			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0100259	PMID:33058759	PCS		8/8			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0000327	PMID:33058759	PCS		1/2			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0006695	PMID:33058759	PCS	HP:0003577				P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0100818	PMID:33058759	PCS		2/3			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0002857	PMID:33058759	PCS		2/2			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0000322	PMID:33058759	PCS		1/2			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0000006	PMID:33058759	PCS					I	HPO:probinson[2021-01-16];HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0000699	PMID:33058759	PCS		1/3			P	HPO:probinson[2021-01-16]
OMIM:619142	Cardioacrofacial dysplasia 1		HP:0000698	PMID:33058759	PCS		1/3			P	HPO:probinson[2021-01-16]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0000011	PMID:22499348	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0002510	PMID:22499348	PCS		1/2			P	HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0001252	PMID:22499348	PCS		1/2			P	HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0001263	PMID:22499348	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0003593	PMID:22499348	PCS		2/2			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0001251	PMID:22499348	PCS		1/2			P	HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0000007	PMID:22499348	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0000648	PMID:22499348	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0011923	PMID:22499348	PCS		2/2			P	HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0001249	PMID:22499348	PCS		1/2			P	HPO:probinson[2022-10-06]
OMIM:618248	Mitochondrial complex I deficiency, nuclear type 27		HP:0000511	PMID:22499348	PCS		1/2			P	HPO:probinson[2022-10-06]
OMIM:158345	Multiple exostoses with spastic tetraparesis		HP:0002762	OMIM:158345	IEA					P	HPO:iea[2009-02-17]
OMIM:158345	Multiple exostoses with spastic tetraparesis		HP:0001285	OMIM:158345	IEA					P	HPO:iea[2009-02-17]
OMIM:158345	Multiple exostoses with spastic tetraparesis		HP:0000006	OMIM:158345	IEA					I	HPO:iea[2009-02-17]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0025066	PMID:19412178	PCS		11/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-01]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0012463	PMID:19412178	PCS		9/9			P	HPO:probinson[2022-09-01]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0001903	PMID:19412178	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0032231	OMIM:205950	IEA					P	HPO:skoehler[2019-02-22]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0003593	OMIM:205950	IEA					C	HPO:skoehler[2010-06-19]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0000007	PMID:19412178	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0001924	PMID:19412178	PCS					P	HPO:probinson[2022-09-01]
OMIM:205950	Anemia, sideroblastic, 2, pyridoxine-refractory		HP:0003281	PMID:19412178	PCS		14/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-01]
OMIM:616265	Peeling skin syndrome 3		HP:0001595	PMID:22289416	PCS		0/7			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-05-21]
OMIM:616265	Peeling skin syndrome 3		HP:0003621	PMID:22289416	PCS		7/7			C	HPO:probinson[2023-05-21]
OMIM:616265	Peeling skin syndrome 3		HP:0000007	PMID:22289416	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2023-05-21]
OMIM:616265	Peeling skin syndrome 3		HP:0000989	PMID:22289416	PCS		0/7			P	HPO:skoehler[2015-09-16];HPO:probinson[2023-05-21]
OMIM:616265	Peeling skin syndrome 3		HP:0010783	PMID:22289416	PCS		0/7			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-05-21]
OMIM:616265	Peeling skin syndrome 3		HP:0040190	PMID:22289416	PCS		7/7			P	HPO:skoehler[2015-09-16];HPO:probinson[2023-05-21]
OMIM:257970	Oculorenocerebellar syndrome		HP:0001264	OMIM:257970	IEA					P	HPO:iea[2009-02-17]
OMIM:257970	Oculorenocerebellar syndrome		HP:0000112	OMIM:257970	IEA					P	HPO:iea[2009-02-17]
OMIM:257970	Oculorenocerebellar syndrome		HP:0001266	OMIM:257970	IEA					P	HPO:iea[2009-02-17]
OMIM:257970	Oculorenocerebellar syndrome		HP:0001939	OMIM:257970	IEA					P	HPO:iea[2009-02-17]
OMIM:257970	Oculorenocerebellar syndrome		HP:0000096	OMIM:257970	IEA					P	HPO:iea[2009-02-17]
OMIM:257970	Oculorenocerebellar syndrome		HP:0000007	OMIM:257970	IEA					I	HPO:iea[2009-02-17]
OMIM:257970	Oculorenocerebellar syndrome		HP:0000546	OMIM:257970	IEA					P	HPO:iea[2009-02-17]
OMIM:257970	Oculorenocerebellar syndrome		HP:0001249	OMIM:257970	IEA					P	HPO:iea[2009-02-17]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0002089	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000463	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0003198	PMID:26004201	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001371	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001196	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0100295	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0010963	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0009760	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0009487	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-12-30]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0100602	PMID:26004201	PCS		1/4			H	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000316	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000219	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000775	OMIM:616503	TAS		HP:0040283			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001561	PMID:26004201	PCS		2/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0003687	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001762	PMID:26004201	PCS		3/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0031013	PMID:26004201	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001060	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001181	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0005280	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0034393	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0034197	PMID:26004201	PCS		1/4			C	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0034198	PMID:26004201	PCS		3/4			C	HPO:probinson[2023-04-20];HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0009473	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0002803	PMID:26004201	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001239	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001558	PMID:26004201	PCS		2/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000007	PMID:26004201	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0002804	PMID:26004201	PCS		4/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0006543	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0001511	PMID:26004201	PCS		2/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0005659	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000325	PMID:26004201	PCS		1/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000347	PMID:26004201	PCS		3/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0000369	PMID:26004201	PCS		2/4			P	HPO:skoehler[2015-08-05]
OMIM:616503	Lethal congenital contracture syndrome 9		HP:0003557	PMID:26004201	PCS		1/4			P	HPO:probinson[2023-04-20]
OMIM:619630	Immunodeficiency 88		HP:0001880	PMID:33296702	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619630	Immunodeficiency 88		HP:0002099	PMID:33296702	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619630	Immunodeficiency 88		HP:0020087	PMID:33296702	PCS	HP:0003593	1/1			P	HPO:probinson[2022-01-24]
OMIM:619630	Immunodeficiency 88		HP:0003593	PMID:33296702	PCS		1/1			C	HPO:probinson[2022-01-24]
OMIM:619630	Immunodeficiency 88		HP:0000007	PMID:33296702	PCS					I	HPO:probinson[2022-01-24]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0003477	OMIM:600361	TAS					P	HPO:skoehler[2012-11-20]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0001276	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0003431	OMIM:600361	PCS				HP:0012825	P	HPO:probinson[2012-03-12]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0001761	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0001288	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0003487	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0003693	OMIM:600361	TAS					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0003581	OMIM:600361	TAS					C	HPO:skoehler[2012-11-20]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0002460	OMIM:600361	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2012-09-18]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0012514	OMIM:600361	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0003690	OMIM:600361	TAS					P	HPO:skoehler[2012-11-20]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0001618	OMIM:600361	TAS					P	HPO:skoehler[2012-11-20]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0011463	OMIM:600361	TAS					C	HPO:skoehler[2012-11-20]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0009027	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0002936	OMIM:600361	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0007256	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0000763	OMIM:600361	TAS					P	HPO:skoehler[2015-01-21]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0002359	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0001257	OMIM:600361	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0003677	OMIM:600361	IEA					C	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0000006	OMIM:600361	IEA					I	HPO:probinson[2009-02-17]
OMIM:600361	Hereditary motor and sensory neuropathy V		HP:0001765	OMIM:600361	IEA					P	HPO:probinson[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0001682	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0000023	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0003344	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0200128	OMIM:250951	TAS					P	HPO:skoehler[2013-06-11]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0001263	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0001284	OMIM:250951	TAS					P	HPO:probinson[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0011344	OMIM:250951	TAS					P	HPO:skoehler[2013-05-29]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0007033	OMIM:250951	TAS					P	HPO:probinson[2013-11-24]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0000954	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0000007	OMIM:250951	IEA					I	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0001319	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0000028	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:250951	3-@methylglutaconic aciduria, type IV		HP:0002643	OMIM:250951	IEA					P	HPO:iea[2009-02-17]
OMIM:613453	Deafness, autosomal recessive 91		HP:0000007	OMIM:613453	TAS					I	HPO:probinson[2013-01-09]
OMIM:613453	Deafness, autosomal recessive 91		HP:0001730	OMIM:613453	TAS					P	HPO:probinson[2013-06-02]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0003577	PMID:10973238	PCS		7/7			C	HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0003241	OMIM:605231	TAS					P	HPO:skoehler[2014-11-26]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0000580	PMID:10973238	PCS		7/7			P	HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0000819	PMID:10973238	PCS		4/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0100259	PMID:10973238	PCS		7/7			P	HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0000107	PMID:10973238	PCS		2/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0000007	PMID:10973238	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0000510	PMID:10973238	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0001159	OMIM:605231	TAS					P	HPO:skoehler[2014-11-26]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0000047	PMID:10973238	PCS		1/3	MALE		P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0001249	PMID:10973238	PCS		6/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0001513	PMID:10973238	PCS		7/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-30]
OMIM:605231	Bardet-Biedl syndrome 6		HP:0000148	PMID:10973238	PCS		1/4	FEMALE		P	HPO:probinson[2022-09-30];HPO:probinson[2022-09-30]
OMIM:615022	Ichthyosis, congenital, autosomal recessive 7		HP:0008064	OMIM:615022	TAS		3/3			P	HPO:probinson[2015-05-10]
OMIM:615022	Ichthyosis, congenital, autosomal recessive 7		HP:0025114	OMIM:615022	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615022	Ichthyosis, congenital, autosomal recessive 7		HP:0025092	OMIM:615022	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615022	Ichthyosis, congenital, autosomal recessive 7		HP:0000007	OMIM:615022	TAS					I	HPO:probinson[2015-05-10]
OMIM:615022	Ichthyosis, congenital, autosomal recessive 7		HP:0001019	OMIM:615022	TAS		3/3			P	HPO:probinson[2015-05-10]
OMIM:615022	Ichthyosis, congenital, autosomal recessive 7		HP:0000982	OMIM:615022	TAS		3/3			P	HPO:probinson[2015-05-10]
OMIM:273150	Testes, rudimentary		HP:0000815	OMIM:273150	IEA					P	HPO:iea[2009-02-17]
OMIM:273150	Testes, rudimentary		HP:0000050	OMIM:273150	IEA					P	HPO:iea[2009-02-17]
OMIM:273150	Testes, rudimentary		HP:0000007	OMIM:273150	IEA					I	HPO:iea[2009-02-17]
OMIM:273150	Testes, rudimentary		HP:0008734	OMIM:273150	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0003236	PMID:15236414	PCS		2/2			P	HPO:probinson[2012-04-01];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0007759	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000486	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000485	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001250	PMID:15236414	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0006829	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001290	PMID:15236414	PCS	HP:0003577	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0003194	PMID:15236414	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000518	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000639	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000557	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000238	PMID:15236414	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001324	OMIM:253280	PCS					P	HPO:probinson[2012-04-01]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0003324	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000252	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0002353	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001263	PMID:15236414	PCS		2/2			P	HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0002350	OMIM:253280	TAS					P	HPO:skoehler[2012-11-20]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0003560	OMIM:253280	PCS					P	HPO:probinson[2012-04-01]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0011800	PMID:15236414	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0007033	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0008045	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000007	OMIM:253280	IEA					I	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000568	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000648	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001257	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001336	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0003577	OMIM:253280	IEA					C	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0007738	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0002365	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000980	OMIM:253280	TAS					P	HPO:skoehler[2012-11-20]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0007260	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0002119	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001302	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000654	OMIM:253280	PCS					P	HPO:probinson[2012-04-01]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001105	OMIM:253280	TAS					P	HPO:skoehler[2012-11-20]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000550	OMIM:253280	TAS					P	HPO:skoehler[2012-11-20]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0001321	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000232	PMID:15236414	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000272	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0011344	OMIM:253280	PCS					P	HPO:probinson[2012-04-01]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0007370	OMIM:253280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0007770	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000546	OMIM:253280	IEA					P	HPO:iea[2009-02-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0007973	OMIM:253280	TAS					P	HPO:skoehler[2012-11-20]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000589	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000501	PMID:15236414	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000347	PMID:15236414;OMIM:253280	PCS		12/12		HP:0012825	P	HPO:probinson[2021-05-09];HPO:probinson[2012-04-01]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0000545	PMID:15236414	PCS	HP:0003577	2/2		HP:0012828	P	HP:probinson[2018-07-08];HPO:probinson[2021-05-09]
OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3		HP:0002126	OMIM:253280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0007814	PMID:17516023	PCS		4/6			P	HPO:probinson[2024-03-09]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0000483	PMID:17516023	PCS		5/6			P	HPO:probinson[2024-03-09]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0001419	PMID:17516023	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2024-03-09]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0003593	PMID:17516023	PCS		1/1			C	HPO:probinson[2024-03-09]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0000646	PMID:17516023	PCS					P	HPO:probinson[2013-02-24];HPO:probinson[2024-03-09]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0007894	PMID:17516023	PCS		0/6			P	HPO:probinson[2013-02-24];HPO:probinson[2024-03-09]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0007663	PMID:17516023	PCS		6/6			P	HPO:probinson[2024-03-09]
OMIM:300814	Nystagmus 6, congenital, X-linked		HP:0000666	PMID:17516023	PCS		5/6			P	HPO:probinson[2013-02-24];HPO:probinson[2024-03-09]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0002168	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001298	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0003236	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001399	OMIM:607426	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0003652	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000100	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001250	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001272	PMID:16400613	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001252	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001251	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0003593	PMID:16400613	PCS		1/1			C	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001270	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000639	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000815	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001903	OMIM:607426	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001328	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000510	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001249	OMIM:607426	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0003128	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000572	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0003323	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0002015	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0002133	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0003200	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0002572	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001260	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001263	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000097	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000096	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0040293	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0002172	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000093	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0034369	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0012378	OMIM:607426	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000407	OMIM:607426	IEA					P	HPO:iea[2009-02-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001639	OMIM:607426	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0002506	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0000007	PMID:16400613	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0002505	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001337	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001876	OMIM:607426	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607426	Coenzyme Q10 deficiency, primary, 1		HP:0001336	PMID:16400613	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000286	PMID:30661772	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000243	PMID:30661772	PCS		1/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000463	PMID:30661772	PCS		3/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0002263	PMID:30661772	PCS		4/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001272	PMID:30661772	PCS		1/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0003196	PMID:30661772	PCS		1/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001290	PMID:30661772	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001629	PMID:30661772	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0012471	PMID:30661772	PCS		2/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000696	PMID:30661772	PCS		1/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000358	PMID:30661772	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001601	PMID:30661772	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001249	PMID:30661772	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000154	PMID:30661772	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0008936	PMID:30661772	PCS		1/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000252	PMID:30661772	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000750	PMID:30661772	PCS		4/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0031936	PMID:30661772	PCS		3/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0011968	PMID:30661772	PCS		2/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001285	PMID:30661772	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001263	PMID:30661772	PCS		4/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0100876	PMID:30661772	PCS		3/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0001838	PMID:30661772	PCS		1/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0004209	PMID:30661772	PCS		4/4			P	HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000369	PMID:30661772	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618506	Coffin-Siris syndrome 10		HP:0000006	PMID:30661772	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0003577	PMID:28119487	PCS		4/16			C	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001195	PMID:28119487	PCS		1/15			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001250	PMID:28119487	PCS		7/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0002020	PMID:28119487	PCS		9/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0003593	PMID:28119487	PCS		10/16			C	HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0045074	PMID:28119487	PCS		8/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001629	PMID:28119487	PCS	HP:0003577	1/17			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0002558	PMID:28119487	PCS		1/17			P	HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001249	PMID:28119487	PCS		17/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0003623	PMID:28119487	PCS		2/16			C	HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000154	PMID:28119487	PCS		13/17			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000252	PMID:28119487	PCS		3/17			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0002059	PMID:28119487	PCS		3/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000750	PMID:28119487	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0002650	PMID:28119487	PCS		2/17			P	HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001382	PMID:28119487	PCS		5/16			P	HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0011968	PMID:28119487	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000490	PMID:28119487	PCS		14/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001263	PMID:28119487	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001518	PMID:28119487	PCS		2/15			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0010880	PMID:28119487	PCS		1/15			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0007099	PMID:28119487	PCS		1/17			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000729	PMID:28119487	PCS		7/17			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000426	PMID:28119487	PCS		7/17			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001319	PMID:28119487	PCS	HP:0003623	4/17			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0001511	PMID:28119487	PCS		3/17			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0006304	PMID:28119487	PCS		4/17			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000028	PMID:28119487	PCS		2/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:617635	Intellectual developmental disorder, autosomal dominant 47		HP:0000006	PMID:28119487	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-08]
OMIM:620099	Cleidocranial dysplasia 2		HP:0003577	PMID:36241386	PCS		1/7			C	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000365	PMID:36241386	PCS		2/7			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000260	PMID:36241386	PCS		2/5			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000680	PMID:36241386	PCS		2/7			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0001508	PMID:36241386	PCS		1/8			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0011463	PMID:36241386	PCS		3/7			C	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0011220	PMID:36241386	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000938	PMID:36241386	PCS		1/8			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0011462	PMID:36241386	PCS		1/7			C	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0009882	PMID:36241386	PCS		3/3			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0002857	PMID:36241386	PCS		1/8			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0200021	PMID:36241386	PCS		2/7			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0001763	PMID:36241386	PCS		2/8			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000894	PMID:36241386	PCS		1/7			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0003621	PMID:36241386	PCS		2/7			C	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0002673	PMID:36241386	PCS		1/8			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0001263	PMID:36241386	PCS		3/6			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0011069	PMID:36241386	PCS		2/7			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0011304	PMID:36241386	PCS		2/8			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0006660	PMID:36241386	PCS		1/7			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000327	PMID:36241386	PCS		2/5			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0006585	PMID:36241386	PCS		5/7			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000307	PMID:36241386	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0001357	PMID:36241386	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0008788	PMID:36241386	PCS		2/6			P	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0000006	PMID:36241386	PCS					I	HPO:probinson[2023-03-04]
OMIM:620099	Cleidocranial dysplasia 2		HP:0001216	PMID:36241386	PCS		3/3			P	HPO:probinson[2023-03-04]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0002521	PMID:23934111	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0002376	PMID:23934111	PCS	HP:0011463	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0002079	PMID:23934111	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0001250	PMID:23934111	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0100704	PMID:23934111	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0001263	PMID:23934111	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0001252	PMID:23934111	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0003593	PMID:23934111	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0001251	PMID:23934111	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0200134	PMID:23934111	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617153	Epileptic encephalopathy, early infantile, 45		HP:0000006	PMID:23934111	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0001030	OMIM:176090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0010473	OMIM:176090	TAS					P	HPO:probinson[2014-01-04]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0001395	OMIM:176090	IEA					P	HPO:iea[2009-02-17]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0000998	OMIM:176090	IEA					P	HPO:iea[2009-02-17]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0000953	OMIM:176090	IEA					P	HPO:iea[2009-02-17]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0000964	OMIM:176090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0000006	OMIM:176090	IEA					I	HPO:iea[2009-02-17]
OMIM:176090	Porphyria cutanea tarda, type I		HP:0030955	OMIM:176090	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0006813	PMID:24623842	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0002133	PMID:24623842	PCS		3/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0002373	PMID:24623842	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0002384	PMID:24623842	PCS		4/4			P	HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0002121	PMID:24623842	PCS		3/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0010819	PMID:24623842	PCS		2/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0001263	PMID:24623842	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0003593	PMID:24623842	PCS		4/4			C	HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0032794	PMID:24623842	PCS		2/4			P	HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0010852	PMID:24623842	PCS		1/4			P	HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0010850	PMID:24623842	PCS		2/4			P	HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0200134	PMID:24623842	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0001249	PMID:24623842	PCS		3/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2021-10-21]
OMIM:615744	Epileptic encephalopathy, early infantile, 19		HP:0000006	PMID:24623842	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-21]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0001892	OMIM:277450	TAS	HP:0003623				P	HPO:probinson[2009-02-17]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0001342	PMID:9845520	PCS		1/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0005543	PMID:9845520	PCS		1/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0011858	PMID:9845520	PCS		4/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0003196	OMIM:277450	IEA					P	HPO:iea[2009-02-17]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0003593	PMID:9845520	PCS		1/4			C	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0031364	PMID:9845520	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0005261	PMID:9845520	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0010655	OMIM:277450	IEA					P	HPO:iea[2009-02-17]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0008151	PMID:9845520	PCS		4/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0008321	PMID:9845520	PCS		4/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0009882	OMIM:277450	IEA					P	HPO:iea[2009-02-17]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0008169	PMID:9845520	PCS		4/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0000007	PMID:9845520	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0000978	OMIM:277450	IEA					P	HPO:iea[2009-02-17]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0000421	OMIM:277450	IEA					P	HPO:iea[2009-02-17]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0002910	PMID:9845520	PCS		0/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0004855	PMID:9845520	PCS		4/4			P	HPO:probinson[2022-09-22]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0003645	OMIM:277450	IEA					P	HPO:iea[2009-02-17]
OMIM:277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1		HP:0003623	PMID:9845520	PCS		3/4			C	HPO:probinson[2022-09-22]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0002015	OMIM:615750	TAS		1/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0002571	PMID:24581742	PCS		9/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0002197	PMID:24581742	PCS		1/9			P	HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0002140	PMID:24581742	PCS		4/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0030880	PMID:24581742	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0003593	PMID:24581742	PCS		2/9			C	HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0011834	PMID:24581742	PCS		3/5			P	HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0033505	PMID:24581742	PCS		1/4			P	HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0011463	PMID:24581742	PCS		5/9			C	HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0000965	OMIM:615750	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0000822	PMID:24581742	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0000007	PMID:24581742	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0000802	OMIM:615750	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0001269	PMID:24581742	PCS		4/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0001873	PMID:24581742	PCS		1/4			P	HPO:probinson[2023-02-09]
OMIM:615750	Moyamoya disease 6 with achalasia		HP:0003623	PMID:24581742	PCS		2/9			C	HPO:probinson[2023-02-09]
OMIM:605543	Parkinson disease 4		HP:0100315	PMID:14593171	PCS					P	HPO:probinson[2012-07-19];HPO:probinson[2021-02-26]
OMIM:605543	Parkinson disease 4		HP:0001300	OMIM:605543	TAS					P	HPO:probinson[2009-02-17]
OMIM:605543	Parkinson disease 4		HP:0001278	OMIM:605543	TAS					P	HPO:probinson[2009-02-17]
OMIM:605543	Parkinson disease 4		HP:0003596	OMIM:605543	IEA					C	HPO:probinson[2009-02-17]
OMIM:605543	Parkinson disease 4		HP:0012332	OMIM:605543	TAS					P	HPO:probinson[2012-07-19]
OMIM:605543	Parkinson disease 4		HP:0000738	OMIM:605543	TAS					P	HPO:probinson[2009-02-17]
OMIM:605543	Parkinson disease 4		HP:0000726	OMIM:605543	TAS					P	HPO:probinson[2009-02-17]
OMIM:605543	Parkinson disease 4		HP:0011999	OMIM:605543	TAS					P	HPO:probinson[2012-07-21]
OMIM:605543	Parkinson disease 4		HP:0001824	OMIM:605543	TAS					P	HPO:probinson[2009-02-17]
OMIM:605543	Parkinson disease 4		HP:0000006	PMID:14593171	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:605543	Parkinson disease 4		HP:0003678	OMIM:605543	IEA					C	HPO:probinson[2009-02-17]
OMIM:615988	Bardet-Biedl syndrome 11		HP:0000077	OMIM:615988	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615988	Bardet-Biedl syndrome 11		HP:0003577	PMID:16606853	PCS					C	HPO:probinson[2022-07-01]
OMIM:615988	Bardet-Biedl syndrome 11		HP:0000007	PMID:16606853	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-01]
OMIM:615988	Bardet-Biedl syndrome 11		HP:0010442	PMID:16606853	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:615988	Bardet-Biedl syndrome 11		HP:0000488	PMID:16606853	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:615988	Bardet-Biedl syndrome 11		HP:0000135	PMID:16606853	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:615988	Bardet-Biedl syndrome 11		HP:0001513	PMID:16606853	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:144750	Hyperostosis, endosteal		HP:0000002	PMID:12579474	PCS		0/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:144750	Hyperostosis, endosteal		HP:0100861	OMIM:144750	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0100774	OMIM:144750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:144750	Hyperostosis, endosteal		HP:0100923	OMIM:144750	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0001507	OMIM:144750	IEA					P	HPO:iea[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0006174	OMIM:144750	IEA					P	HPO:iea[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0000407	OMIM:144750	IEA					P	HPO:iea[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0000935	OMIM:144750	IEA					P	HPO:iea[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0100789	PMID:12579474	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-04]
OMIM:144750	Hyperostosis, endosteal		HP:0008114	OMIM:144750	IEA					P	HPO:iea[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0000689	OMIM:144750	TAS					P	HPO:probinson[2012-04-28]
OMIM:144750	Hyperostosis, endosteal		HP:0000006	PMID:12579474	PCS					I	HPO:probinson[2012-04-28];HPO:probinson[2024-03-08]
OMIM:144750	Hyperostosis, endosteal		HP:0002644	OMIM:144750	IEA					P	HPO:iea[2009-02-17]
OMIM:144750	Hyperostosis, endosteal		HP:0004425	OMIM:144750	TAS					P	HPO:probinson[2012-04-28]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000044	PMID:18559922	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000054	OMIM:610628	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0001250	PMID:18559922	PCS		1/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0032466	PMID:18559922	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000819	PMID:18559922	PCS		1/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000939	PMID:18559922	PCS		2/8			P	HPO:probinson[2022-09-12];HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0008197	PMID:18559922	PCS		3/3			P	HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0003829	OMIM:610628	TAS					I	HPO:skoehler[2015-12-30]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000458	OMIM:610628	TAS		1/4			P	HPO:probinson[2013-04-01];HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0004409	PMID:18559922	PCS		2/4			P	HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0008734	OMIM:610628	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0001335	PMID:18559922	PCS		1/4			P	HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000006	PMID:18559922	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000028	PMID:18559922	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0001513	OMIM:610628	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:610628	Hypogonadotropic hypogonadism 4 with or without anosmia		HP:0000786	OMIM:610628	TAS					P	HPO:skoehler[2014-11-26]
OMIM:109650	Behcet syndrome		HP:0031615	OMIM:109650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:109650	Behcet syndrome		HP:0002232	OMIM:109650	IEA					P	HPO:iea[2009-02-17]
OMIM:109650	Behcet syndrome		HP:0000155	OMIM:109650	TAS					P	HPO:skoehler[2009-02-17]
OMIM:109650	Behcet syndrome		HP:0001101	OMIM:109650	IEA					P	HPO:iea[2009-02-17]
OMIM:109650	Behcet syndrome		HP:0000031	OMIM:109650	TAS					P	HPO:probinson[2009-02-17]
OMIM:109650	Behcet syndrome		HP:0030880	OMIM:109650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:109650	Behcet syndrome		HP:0001094	OMIM:109650	IEA					P	HPO:iea[2009-02-17]
OMIM:109650	Behcet syndrome		HP:0410060	PMID:29099052	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:109650	Behcet syndrome		HP:0012219	OMIM:109650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:109650	Behcet syndrome		HP:0010783	OMIM:109650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:109650	Behcet syndrome		HP:0012424	OMIM:109650	TAS					P	HPO:probinson[2015-07-19]
OMIM:109650	Behcet syndrome		HP:0000737	OMIM:109650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:109650	Behcet syndrome		HP:0002638	OMIM:109650	IEA					P	HPO:iea[2009-02-17]
OMIM:109650	Behcet syndrome		HP:0000007	PMID:12955762	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:109650	Behcet syndrome		HP:0001369	OMIM:109650	IEA					P	HPO:iea[2009-02-17]
OMIM:109650	Behcet syndrome		HP:0003249	OMIM:109650	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607432	Lissencephaly 1		HP:0008936	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0003577	PMID:11754098	PCS					C	HPO:probinson[2022-07-19]
OMIM:607432	Lissencephaly 1		HP:0001321	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0002365	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0032409	OMIM:607432	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607432	Lissencephaly 1		HP:0001250	OMIM:607432	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607432	Lissencephaly 1		HP:0001263	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0001285	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0005484	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0031882	OMIM:607432	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607432	Lissencephaly 1		HP:0002282	OMIM:607432	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607432	Lissencephaly 1		HP:0012520	OMIM:607432	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607432	Lissencephaly 1		HP:0001339	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0002119	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0001302	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0003745	OMIM:607432	IEA					I	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0002500	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607432	Lissencephaly 1		HP:0000006	OMIM:607432	IEA					I	HPO:skoehler[2019-04-18]
OMIM:607432	Lissencephaly 1		HP:0001249	OMIM:607432	IEA					P	HPO:skoehler[2010-06-19]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0001250	OMIM:618512	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0001273	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0003593	OMIM:618512	IEA					C	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0012448	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0001290	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000718	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0011220	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000739	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000256	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0006579	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000494	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000750	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0031936	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0002013	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0011968	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000293	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000490	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0001263	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0001182	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0012166	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0002808	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000629	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0001999	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0200134	OMIM:618512	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0100716	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000268	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0002500	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000028	OMIM:618512	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618512	O'donnell-Luria-Rodan syndrome		HP:0000006	PMID:31079897	PCS					I	HPO:probinson[2020-07-17]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0003212	PMID:22010916	PCS		2/2			P	HPO:probinson[2020-10-10];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0200039	PMID:22010916	PCS	HP:0003623	2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0025085	PMID:22010916	PCS	HP:0003623	2/2			P	HPO:probinson[2020-10-10];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0033117	PMID:22010916	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0033194	PMID:22010916	PCS		2/2			P	HPO:probinson[2020-10-12]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0033195	PMID:22010916	PCS		2/2			P	HPO:probinson[2020-10-12]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0001805	PMID:22010916	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0001508	PMID:22010916	PCS		1/2			P	HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0011473	PMID:22010916	PCS	HP:0011463	1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0001818	PMID:22010916	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0001019	PMID:22010916	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0000007	PMID:22010916	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0000498	PMID:22010916	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-10]
OMIM:614328	Inflammatory skin and bowel disease, neonatal, 1		HP:0410017	PMID:22010916	PCS	HP:0003593	2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-10-10]
OMIM:261540	Peters-plus syndrome		HP:0004325	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000365	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0000089	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0002263	PMID:12119218	PCS		48/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000480	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0010049	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000518	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000639	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0002937	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000238	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0008897	OMIM:261540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261540	Peters-plus syndrome		HP:0009623	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001169	PMID:12119218	PCS		49/49			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000358	OMIM:261540	IEA					P	HPO:skoehler[2019-09-07]
OMIM:261540	Peters-plus syndrome		HP:0000252	PMID:12119218	PCS		11/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000013	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000767	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000007	PMID:16909395	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0004209	PMID:12119218	PCS		45/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000369	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0000402	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000126	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000582	PMID:12119218	PCS		17/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000343	PMID:12119218	PCS		45/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0008905	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001156	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0001274	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000060	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0008873	PMID:16909395	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0008872	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000612	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000219	OMIM:261540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261540	Peters-plus syndrome		HP:0002119	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000059	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0006610	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001545	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0002996	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001561	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000475	PMID:12119218	PCS		36/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0002650	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0004279	PMID:12119218	PCS		49/49			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000233	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000073	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000470	OMIM:261540	IEA					P	HPO:skoehler[2019-04-18]
OMIM:261540	Peters-plus syndrome		HP:0000508	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0002007	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001159	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000465	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000501	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000347	PMID:12119218	PCS		22/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0002644	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001831	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0008726	OMIM:261540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261540	Peters-plus syndrome		HP:0001773	OMIM:261540	IEA					P	HPO:skoehler[2010-06-20]
OMIM:261540	Peters-plus syndrome		HP:0000200	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0003278	OMIM:261540	TAS					P	HPO:skoehler[2013-04-18]
OMIM:261540	Peters-plus syndrome		HP:0001250	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0011220	PMID:12119218	PCS		34/49			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0011065	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000316	PMID:12119218	PCS		37/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000954	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0005608	OMIM:261540	TAS					P	HPO:skoehler[2014-06-24]
OMIM:261540	Peters-plus syndrome		HP:0001769	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0002219	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001643	OMIM:261540	IEA					P	HPO:skoehler[2019-04-18]
OMIM:261540	Peters-plus syndrome		HP:0001642	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000311	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001540	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000175	PMID:16909395	PCS		7/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0003561	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001382	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001263	PMID:12119218	PCS		41/49			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000690	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0100336	PMID:16909395	PCS		3/20			P	HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000327	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0001537	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0008569	PMID:12119218	PCS		21/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000047	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000204	PMID:16909395	PCS		5/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000687	OMIM:261540	IEA					P	HPO:skoehler[2019-04-18]
OMIM:261540	Peters-plus syndrome		HP:0004467	PMID:12119218	PCS		18/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000260	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0010743	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001629	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000659	PMID:12119218;PMID:16909395	PCS		51/68			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0000411	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000256	PMID:12119218	PCS		4/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0002059	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001363	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000276	OMIM:261540	IEA					P	HPO:skoehler[2019-02-22]
OMIM:261540	Peters-plus syndrome		HP:0001761	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-Plus syndrome		HP:0045025	PMID:12119218	PCS		38/49			P	HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0001080	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0001511	PMID:12119218	PCS		43/49			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:261540	Peters-plus syndrome		HP:0001631	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000028	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:261540	Peters-plus syndrome		HP:0000545	OMIM:261540	IEA					P	HPO:iea[2009-02-17]
OMIM:112270	Bone pain, periodic		HP:0002653	OMIM:112270	TAS					P	HPO:probinson[2009-02-17]
OMIM:112270	Bone pain, periodic		HP:0000006	OMIM:112270	IEA					I	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0001034	PMID:35837079	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0001891	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0002584	PMID:35837079	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0032454	PMID:28445255;PMID:35837079;PMID:35782219;PMID:35919209	PCS		13/13			P	HP:probinson[2019-04-19];HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0010784	OMIM:175200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:175200	Peutz-Jeghers syndrome		HP:0025085	PMID:35919209	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0011463	PMID:35837079;PMID:35782219;PMID:35919209	PCS		3/3			C	HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0000138	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0002894	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0002576	PMID:35837079;PMID:35782219	PCS		2/2			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0002672	PMID:3587280	PCS		4/31			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:175200	Peutz-Jeghers syndrome		HP:0003002	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0002035	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0000771	OMIM:175200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0004394	PMID:35919209	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0100582	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0001080	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0004390	PMID:35782219	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0031261	OMIM:175200	TAS					P	HP:probinson[2019-04-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0100759	OMIM:175200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0034352	OMIM:175200	TAS					P	HPO:probinson[2022-09-05]
OMIM:175200	Peutz-Jeghers syndrome		HP:0032451	PMID:28445255;PMID:35782219;PMID:35919209	PCS		12/12			P	HP:probinson[2019-04-19];HPO:probinson[2022-08-20]
OMIM:175200	Peutz-Jeghers syndrome		HP:0001217	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0008204	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0000069	OMIM:175200	IEA					P	HPO:iea[2009-02-17]
OMIM:175200	Peutz-Jeghers syndrome		HP:0000006	PMID:28445255	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:175200	Peutz-Jeghers syndrome		HP:0002027	PMID:35837079;PMID:35919209	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002069	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0003577	PMID:35858628	PCS		4/5			C	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0000486	PMID:35858628	PCS		3/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002188	PMID:35858628	PCS		2/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002540	PMID:35858628	PCS		2/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001272	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002283	PMID:35858628	PCS		3/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001252	PMID:35858628	PCS		5/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0011577	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0033725	PMID:35858628	PCS		4/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0000639	PMID:35858628	PCS		3/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001629	PMID:35858628	PCS		2/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002719	PMID:35858628	PCS		3/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0100704	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001647	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002119	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001249	PMID:35858628	PCS					P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0003623	PMID:35858628	PCS		1/5			C	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0000252	PMID:35858628	PCS		5/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001344	PMID:35858628	PCS		4/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002078	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001684	PMID:35858628	PCS		2/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001640	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0011968	PMID:35858628	PCS		2/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0002197	PMID:35858628	PCS		2/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0010819	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0011705	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001263	PMID:35858628	PCS		5/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001680	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0005165	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0011003	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0005180	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0010880	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0006682	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0000007	PMID:35858628	PCS					I	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001635	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001659	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001631	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:620066	Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment		HP:0001653	PMID:35858628	PCS		1/5			P	HPO:probinson[2022-10-02]
OMIM:300633	Hypospadias 1, X-linked		HP:0003577	PMID:8097257	PCS		2/2			C	HPO:probinson[2023-06-10]
OMIM:300633	Hypospadias 1, X-linked		HP:0000051	PMID:8097257	PCS		2/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2023-06-10]
OMIM:300633	Hypospadias 1, X-linked		HP:0001419	PMID:8097257	PCS					I	HPO:skoehler[2012-10-16];HPO:probinson[2023-06-10]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001572	PMID:35047834	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000486	PMID:35047834	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001773	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0004322	PMID:35047834	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001250	PMID:35047834	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0012389	PMID:35047834	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0008770	PMID:35047834	PCS		4/10			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002816	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000717	PMID:35047834	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000316	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0003307	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0003701	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002019	PMID:35047834	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001763	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000358	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000252	PMID:35047834	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000175	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000574	PMID:35047834	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002750	PMID:35047834	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001263	PMID:35047834	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002194	PMID:35047834	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0012378	PMID:35047834	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000007	PMID:35047834	PCS					I	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000527	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001258	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000189	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000463	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002162	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0010862	PMID:35047834	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000938	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000739	PMID:35047834	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0009882	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000219	PMID:35047834	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0030084	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0008936	PMID:35047834	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002015	PMID:35047834	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000750	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002376	PMID:35047834	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0031936	PMID:35047834	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001761	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0003025	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000470	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0005280	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0010536	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0002808	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000508	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000348	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000307	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001511	PMID:35047834	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0007018	PMID:35047834	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000545	PMID:35047834	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0000303	PMID:35047834	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001238	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620700	Intellectual developmental disorder, autosomal recessive 81		HP:0001831	PMID:35047834	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:300155	Retinitis pigmentosa 24		HP:0008020	OMIM:300155	IEA			MALE		P	HPO:skoehler[2013-01-11]
OMIM:300155	Retinitis pigmentosa 24		HP:0001417	OMIM:300155	IEA					I	HPO:skoehler[2013-01-11]
OMIM:300155	Retinitis pigmentosa 24		HP:0000510	OMIM:300155	IEA	HP:0003621				P	HPO:skoehler[2013-01-09]
OMIM:615963	Vesicoureteral reflux 8		HP:0000010	PMID:23620400	PCS		8/8			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-02]
OMIM:615963	Vesicoureteral reflux 8		HP:0000076	PMID:23620400	PCS		5/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-02]
OMIM:615963	Vesicoureteral reflux 8		HP:0001382	PMID:23620400	PCS		2/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-02]
OMIM:615963	Vesicoureteral reflux 8		HP:0000081	PMID:23620400	PCS		5/9			P	HPO:skoehler[2014-10-06]
OMIM:615963	Vesicoureteral reflux 8		HP:0000006	PMID:23620400	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-02]
OMIM:620714	Deafness, autosomal recessive 122		HP:0000407	PMID:37943620	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620714	Deafness, autosomal recessive 122		HP:0003581	PMID:37943620	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620714	Deafness, autosomal recessive 122		HP:0000007	PMID:37943620	PCS					I	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001177	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0004322	PMID:35213692	PCS		3/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001156	PMID:35213692	PCS		4/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000160	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001252	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0012133	PMID:35213692	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001903	PMID:35213692	PCS		6/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000316	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001822	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0002857	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0007687	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000411	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001763	PMID:35213692	PCS		3/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000252	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001385	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000494	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0003764	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24];HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001684	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000293	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001182	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0011228	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0040023	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000349	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000965	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000007	PMID:35213692	PCS					I	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0002669	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0002967	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0002208	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001659	PMID:35213692	PCS		1/3			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001852	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000664	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001873	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000369	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0000347	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001513	PMID:35213692	PCS		4/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0001831	PMID:35213692	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620072	Diamond-Blackfan anemia 21		HP:0002028	PMID:35213692	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:302030	Calvarial hyperostosis		HP:0000463	PMID:24145306	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:302030	Calvarial hyperostosis		HP:0011463	PMID:24145306	PCS		3/3			C	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:302030	Calvarial hyperostosis		HP:0001419	PMID:24145306	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-09]
OMIM:302030	Calvarial hyperostosis		HP:0000348	PMID:24145306	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:302030	Calvarial hyperostosis		HP:0034975	PMID:24145306	PCS		2/3			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:302030	Calvarial hyperostosis		HP:0004490	PMID:24145306	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:302030	Calvarial hyperostosis		HP:0005280	PMID:24145306	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000286	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001396	OMIM:610199	TAS					P	HPO:probinson[2013-03-31]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0025484	PMID:16715098	PCS		3/3			P	HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000343	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0031507	PMID:16715098	PCS		3/3			P	HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0004442	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000260	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001395	PMID:16715098	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0002240	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000819	PMID:16715098	PCS	HP:0003623	6/6			P	HPO:probinson[2013-01-09];HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001409	OMIM:610199	TAS		12/20			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0002719	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000938	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000557	PMID:16715098	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000219	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000851	PMID:16715098	PCS	HP:0003623	6/6			P	HPO:probinson[2013-03-31];HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000113	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001744	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0003623	PMID:16715098	PCS		6/6			C	HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0002036	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000453	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0030423	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0025379	PMID:16715098	PCS		0/4			P	HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0002594	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0007906	PMID:16715098	PCS		2/4			P	HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001087	OMIM:610199	TAS					P	HPO:probinson[2013-03-31]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001263	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0005280	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0012115	OMIM:610199	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000407	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000107	PMID:16715098	PCS		2/6			P	HPO:probinson[2013-03-31];HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001537	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000007	PMID:16715098	PCS					I	HPO:probinson[2013-03-31];HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0002925	PMID:16715098	PCS		6/6			P	HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001737	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0002944	OMIM:610199	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0001511	PMID:16715098	PCS		6/6			P	HPO:probinson[2013-03-31];HPO:probinson[2023-03-27]
OMIM:610199	Diabetes mellitus, neonatal, with congenital hypothyroidism		HP:0000369	OMIM:610199	TAS					P	HPO:skoehler[2017-07-13]
OMIM:619803	Spermatogenic failure 67		HP:0003251	PMID:31985809	PCS		1/1			P	HPO:probinson[2022-05-04]
OMIM:619803	Spermatogenic failure 67		HP:0011462	PMID:31985809	PCS		1/1			C	HPO:probinson[2022-05-04]
OMIM:619803	Spermatogenic failure 67		HP:0000007	PMID:31985809	PCS					I	HPO:probinson[2022-05-04]
OMIM:619803	Spermatogenic failure 67		HP:0012205	PMID:31985809	PCS		1/1			P	HPO:probinson[2022-05-04]
OMIM:612956	Ventricular fibrillation, paroxysmal familial, 2		HP:0001663	PMID:19285295	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2020-09-20]
OMIM:612956	Ventricular fibrillation, paroxysmal familial, 2		HP:0006682	PMID:19285295	PCS					P	HPO:probinson[2020-09-20]
OMIM:612956	Ventricular fibrillation, paroxysmal familial, 2		HP:0001645	PMID:19285295	PCS	HP:0003581	HP:0040283			P	HPO:skoehler[2015-04-19];HPO:probinson[2020-09-20]
OMIM:612956	Ventricular fibrillation, paroxysmal familial, 2		HP:0000006	PMID:19285295	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-20]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0032967	PMID:12672469	PCS					P	HPO:probinson[2020-06-14]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0030169	PMID:7785020	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0033709	PMID:7785020	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0002110	PMID:7785020	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0001394	PMID:7785020	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0002094	OMIM:613490	TAS		29/130			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-06-14]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0012735	PMID:7785020	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0032025	PMID:7785020	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0030828	PMID:28203073	PCS		20/127			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0025708	PMID:7785020	PCS		1/1			C	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0000007	PMID:8831086	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-06-14]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0006510	OMIM:613490	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0002910	OMIM:613490	TAS					P	HPO:skoehler[2013-10-06]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0001744	PMID:7785020	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0004469	PMID:28203073	PCS		7/129			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0002105	PMID:7785020	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:613490	Alpha-1-Antitrypsin deficiency		HP:0001402	OMIM:613490	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0002069	PMID:27773430	PCS		1/13			P	HPO:probinson[2023-03-07]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0001355	OMIM:614499	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0000750	OMIM:614499	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0001250	OMIM:614499	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0040194	PMID:27773430	PCS		11/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0001339	OMIM:614499	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0000007	PMID:27773430	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-03-07]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0001302	OMIM:614499	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614499	Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly		HP:0001249	PMID:27773430	PCS		13/13			P	HPO:probinson[2013-08-10];HPO:probinson[2023-03-07]
OMIM:258470	Ophthalmoplegic neuromuscular disorder with abnormal mitochondria		HP:0000508	OMIM:258470	TAS		20/20			P	HPO:nvasilevsky[2019-02-28];HPO:iea[2009-02-17]
OMIM:258470	Ophthalmoplegic neuromuscular disorder with abnormal mitochondria		HP:0000602	OMIM:258470	IEA					P	HPO:iea[2009-02-17]
OMIM:258470	Ophthalmoplegic neuromuscular disorder with abnormal mitochondria		HP:0001427	OMIM:258470	TAS					I	HPO:nvasilevsky[2019-02-28]
OMIM:258470	Ophthalmoplegic neuromuscular disorder with abnormal mitochondria		HP:0000007	OMIM:258470	TAS					I	HPO:nvasilevsky[2019-02-28]
OMIM:258470	Ophthalmoplegic neuromuscular disorder with abnormal mitochondria		HP:0001291	OMIM:258470	IEA					P	HPO:iea[2009-02-17]
OMIM:258470	Ophthalmoplegic neuromuscular disorder with abnormal mitochondria		HP:0001324	OMIM:258470	IEA					P	HPO:iea[2009-02-17]
OMIM:258470	Ophthalmoplegic neuromuscular disorder with abnormal mitochondria		HP:0008316	OMIM:258470	IEA					P	HPO:iea[2009-02-17]
OMIM:605594	Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1		HP:0008619	OMIM:605594	TAS					P	HPO:skoehler[2009-02-17]
OMIM:605594	Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1		HP:0005101	OMIM:605594	TAS					P	HPO:skoehler[2009-02-17]
OMIM:605594	Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1		HP:0000360	OMIM:605594	TAS					P	HPO:skoehler[2009-02-17]
OMIM:605594	Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1		HP:0000703	OMIM:605594	TAS					P	HPO:skoehler[2009-02-17]
OMIM:605594	Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1		HP:0000006	OMIM:605594	TAS					I	HPO:skoehler[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0001276	PMID:22713811	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0002344	PMID:22713811	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0002100	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0000486	PMID:22713811	PCS		2/4			P	HPO:probinson[2023-01-23];HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0010307	PMID:22713811	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0002483	OMIM:230900	IEA					P	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0001250	OMIM:230900	IEA					P	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0002063	OMIM:230900	IEA					P	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0002020	PMID:22713811	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0002240	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0003593	PMID:22713811	PCS		2/2			C	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0011950	PMID:22713811	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0001508	PMID:22713811	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0001903	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0000657	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0001522	PMID:22713811	PCS		1/2			C	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0001744	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0001347	OMIM:230900	IEA					P	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0002059	OMIM:230900	IEA					P	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0002015	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0000211	OMIM:230900	IEA					P	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0011968	PMID:22713811	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0001263	PMID:22713811	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0012735	PMID:22713811	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0011590	PMID:22713811	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0000602	PMID:22713811	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0000007	OMIM:230900	IEA					I	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0001538	OMIM:230900	TAS					P	HPO:probinson[2012-07-25]
OMIM:230900	Gaucher disease, type II		HP:0000565	OMIM:230900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0001257	OMIM:230900	IEA					P	HPO:iea[2009-02-17]
OMIM:230900	Gaucher disease, type II		HP:0001873	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:230900	Gaucher disease, type II		HP:0002104	PMID:22713811	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:617190	Shashi-Pena syndrome		HP:0000286	PMID:27693232	PCS		3/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0003577	PMID:27693232	PCS		6/6			C	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000122	PMID:27693232	PCS	HP:0030674	1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001250	PMID:27693232	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0025104	PMID:27693232	PCS		2/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001252	PMID:27693232	PCS		6/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0010049	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0006191	PMID:27693232	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000939	PMID:27693232	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000316	PMID:27693232	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000998	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0008872	PMID:27693232	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001943	PMID:27693232	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0002119	PMID:27693232	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000219	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000455	PMID:27693232	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000378	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001643	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000256	PMID:27693232	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000278	PMID:27693232	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001249	PMID:27693232	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000358	PMID:27693232	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0002553	PMID:27693232	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000396	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000750	PMID:27693232	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0002650	PMID:27693232	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000276	PMID:27693232	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0002057	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0002373	PMID:27693232	PCS		3/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001263	PMID:27693232	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0010952	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0034295	PMID:27693232	PCS		2/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0012520	PMID:27693232	PCS		3/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0002808	PMID:27693232	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000508	PMID:27693232	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0002509	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000527	PMID:27693232	PCS		2/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0005616	PMID:27693232	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001511	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000664	PMID:27693232	PCS		2/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0007413	PMID:27693232	PCS		6/6			P	HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0001631	PMID:27693232	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000520	PMID:27693232	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000006	PMID:27693232	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0000369	PMID:27693232	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617190	Shashi-Pena syndrome		HP:0004602	PMID:27693232	PCS		1/6			P	HPO:probinson[2022-11-11]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0000365	PMID:17701900	PCS	HP:0003593	5/5			P	HPO:probinson[2019-04-20]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0001288	OMIM:311070	IEA					P	HPO:iea[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0001761	OMIM:311070	IEA					P	HPO:iea[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0003693	OMIM:311070	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0001271	OMIM:311070	IEA					P	HPO:skoehler[2015-12-30]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0003383	PMID:17701900	PCS					P	HPO:skoehler[2013-05-31];HPO:probinson[2019-04-20]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0002460	OMIM:311070	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0003481	PMID:17701900	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2019-04-20]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0001270	OMIM:311070	IEA					P	HPO:iea[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0032460	PMID:17701900	PCS		3/3			P	HPO:probinson[2019-04-20]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0000529	PMID:17701900	PCS	HP:0003621	5/5			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0011463	OMIM:311070	TAS					C	HPO:probinson[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0000407	OMIM:311070	IEA					P	HPO:iea[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0001419	PMID:17701900	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0003828	OMIM:311070	TAS					M	HPO:skoehler[2017-07-13]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0002936	PMID:17701900	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0000648	OMIM:311070	IEA					P	HPO:iea[2009-02-17]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0000510	OMIM:311070	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:311070	Charcot-Marie-Tooth disease, X-linked recessive, 5		HP:0002522	OMIM:311070	IEA					P	HPO:iea[2009-02-17]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0001265	PMID:27693233	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0003577	PMID:27693233	PCS		7/7			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0002540	PMID:27693233	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0001992	PMID:27693233	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0001250	PMID:27693233	PCS		2/7			P	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0011924	PMID:27693233	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0001290	PMID:27693233	PCS				HP:0012829	P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0002490	PMID:27693233	PCS		6/6			P	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0011923	PMID:27693233	PCS		3/4			P	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0009141	PMID:27693233	PCS		5/5			P	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0001639	PMID:27693233	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0008347	PMID:27693233	PCS		5/5			P	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0002747	PMID:27693233	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0003811	PMID:27693233	PCS		2/7			C	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0001522	PMID:27693233	PCS		3/7			C	HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0000006	PMID:27693233	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:617184	Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant		HP:0003128	PMID:27693233	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0002751	PMID:11992252	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0000473	PMID:11992252	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0001374	PMID:11992252	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0003236	PMID:11992252	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0003577	PMID:11992252	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0031936	PMID:11992252	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0020152	PMID:11992252	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0001252	PMID:11992252	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0003273	PMID:11992252	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0034677	PMID:11992252	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0034671	PMID:11992252	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0003749	PMID:11992252	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0030043	PMID:11992252	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0000007	PMID:11992252	PCS					I	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0003547	PMID:11992252	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0003722	PMID:11992252	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620728	Ullrich congenital muscular dystrophy 1C		HP:0003623	PMID:11992252	PCS		3/5			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:218040	Costello syndrome		HP:0000286	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001771	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0002862	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000486	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0004322	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0002021	OMIM:218040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:218040	Costello syndrome		HP:0002780	OMIM:218040	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218040	Costello syndrome		HP:0000083	OMIM:218040	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:218040	Costello syndrome		HP:0000280	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0006191	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001808	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001609	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000316	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0009588	OMIM:218040	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218040	Costello syndrome		HP:0002859	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000238	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0000953	OMIM:218040	IEA					P	HPO:skoehler[2013-08-09]
OMIM:218040	Costello syndrome		HP:0000956	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0002779	OMIM:218040	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218040	Costello syndrome		HP:0000158	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0003745	OMIM:218040	IEA					I	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001642	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001249	OMIM:218040	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218040	Costello syndrome		HP:0000358	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0000494	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001187	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0003764	OMIM:218040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:218040	Costello syndrome		HP:0002870	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000293	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0002033	OMIM:218040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:218040	Costello syndrome		HP:0001263	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0001816	OMIM:218040	TAS					P	HPO:iea[2013-08-09]
OMIM:218040	Costello syndrome		HP:0001814	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000768	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0002107	OMIM:218040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:218040	Costello syndrome		HP:0000006	OMIM:218040	IEA					I	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000369	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001699	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000463	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001552	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000260	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0011675	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0031842	OMIM:218040	IEA					P	HPO:skoehler[2018-10-08]
OMIM:218040	Costello syndrome		HP:0008070	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001508	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001629	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001548	OMIM:218040	TAS					P	HPO:skoehler[2013-05-31]
OMIM:218040	Costello syndrome		HP:0001943	OMIM:218040	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218040	Costello syndrome		HP:0001869	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0002119	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0002878	OMIM:218040	TAS					P	HPO:skoehler[2014-06-24]
OMIM:218040	Costello syndrome		HP:0000218	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000179	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000256	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0005989	OMIM:218040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:218040	Costello syndrome		HP:0002996	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001622	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0002212	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001561	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0002059	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001762	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000470	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0002093	OMIM:218040	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218040	Costello syndrome		HP:0005280	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001639	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0007099	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0000508	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0012081	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0000307	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218040	Costello syndrome		HP:0000465	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001598	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001631	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0001634	OMIM:218040	IEA					P	HPO:iea[2009-02-17]
OMIM:218040	Costello syndrome		HP:0000347	OMIM:218040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0001892	PMID:24325358	PCS		6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0003593	OMIM:187900	TAS					C	HPO:probinson[2009-02-17]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0003010	PMID:23927492	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0031364	OMIM:187900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0012526	PMID:24325358	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0040185	PMID:23927492;PMID:24325358	PCS		14/14			P	HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0011974	PMID:24325358	PCS		1/1			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0031965	PMID:23927492	PCS		8/8			P	HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0011890	PMID:23927492	PCS		8/8			P	HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0008320	PMID:23927492	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0000007	OMIM:187900	TAS					I	HPO:probinson[2012-05-30]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0000978	PMID:23927492	PCS	HP:0011463	8/8			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0000967	OMIM:187900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0008148	PMID:23927492	PCS		2/2			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0000421	PMID:23927492	PCS	HP:0011463	8/8			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0002239	OMIM:187900	TAS					P	HPO:skoehler[2014-02-25]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0001873	PMID:24325358	PCS		6/6			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0000006	PMID:24325358	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2022-09-22]
OMIM:187900	Bleeding disorder, platelet-type, 17		HP:0003337	OMIM:187900	TAS					P	HPO:probinson[2009-02-17]
OMIM:226810	Celiac disease, epilepsy and cerebral calcification syndrome		HP:0002608	OMIM:226810	IEA					P	HPO:skoehler[2015-01-27]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0003577	PMID:14675179;PMID:9185503	PCS		2/2			C	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0004399	PMID:9185503	PCS	HP:0003577	1/1			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0003341	PMID:14675179;PMID:9185503	PCS		2/2			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0008066	PMID:14675179;PMID:9185503	PCS		2/2			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0007385	PMID:9185503	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0010450	PMID:9185503	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0008551	PMID:14675179	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0000007	PMID:9185503	PCS					I	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0007589	PMID:9185503	PCS	HP:0003577	1/1			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0007589	PMID:14675179	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0003811	PMID:9185503	PCS		1/1			C	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0200097	PMID:14675179	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:619817	Epidermolysis bullosa, junctional 6, with pyloric atresia		HP:0020117	PMID:9185503	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0001058	PMID:34196201	PCS		1/4			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0001382	PMID:34196201	PCS		1/4			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0000639	PMID:35359234	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0001263	PMID:34196201;PMID:35359234	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0003593	PMID:34196201;PMID:35359234	PCS		5/5			C	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0000007	PMID:34196201	PCS					I	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0002317	PMID:35359234	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0012169	PMID:34196201	PCS		1/4			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0001249	PMID:34196201;PMID:35359234	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0002346	PMID:35359234	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:619988	Intellectual developmental disorder, autosomal recessive 77		HP:0001611	PMID:35359234	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001276	PMID:22492876	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0004446	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0002540	OMIM:608885	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0002188	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0004322	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001250	PMID:22492876	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001251	OMIM:608885	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0002240	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0003593	OMIM:608885	TAS					C	HPO:skoehler[2017-07-13]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0011972	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0000518	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0000639	PMID:22492876	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0032660	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0025116	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001249	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0000952	PMID:22492876	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001744	PMID:22492876	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001347	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0007229	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0003623	PMID:22492876	PCS		1/1			C	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0000252	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001561	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001344	OMIM:608885	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0002153	PMID:22492876	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001263	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0030948	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0100018	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0002908	PMID:22492876	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001878	PMID:22492876	PCS		1/1		HP:0025303	P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001510	OMIM:608885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0001257	OMIM:608885	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608885	Stomatin-deficient cryohydrocytosis with neurologic defects		HP:0000006	PMID:22492876	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-08]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000463	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0004322	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0002002	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0003593	PMID:33517393	PCS		1/1			C	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0010885	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0033332	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0011220	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000316	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000998	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0002716	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0006532	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000218	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000256	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000358	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000494	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0004313	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0002650	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0001442	PMID:33517393	PCS					I	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0002099	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000470	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0010614	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0005280	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0011227	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000821	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0001935	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000768	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0002967	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0001653	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0001433	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000006	PMID:33517393	PCS					I	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000303	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619750	Immunodeficiency 94 with autoinflammation and dysmorphic facies		HP:0000369	PMID:33517393	PCS		1/1			P	HPO:probinson[2022-04-17]
DECIPHER:16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0005403	DECIPHER:16	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0000750	DECIPHER:16	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0001627	DECIPHER:16	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0002901	DECIPHER:16	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0001611	DECIPHER:16	IEA					P	HPO:skoehler[2013-05-29]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000286	PMID:10590074;PMID:10753603	PCS		3/60			P	HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000486	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001894	PMID:7267232	PCS		21/38			P	HPO:skoehler[2010-06-18];HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000089	PMID:10590074	PCS		2/55			P	HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0004322	PMID:10590074;PMID:10753603;PMID:35923690	PCS		26/70			P	HPO:probinson[2019-07-18];HPO:skoehler[2010-06-18];HPO:probinson[2019-07-18];HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0003593	OMIM:105650	IEA					C	HPO:skoehler[2010-06-19]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0010446	PMID:10590074	PCS		2/55			P	HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0011463	PMID:35923690	PCS		2/10			C	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0011462	PMID:35923690	PCS		2/10			C	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000316	PMID:10753603;PMID:35923690	PCS		2/15			P	HPO:probinson[2019-07-18];HPO:skoehler[2010-06-18];HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000878	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0009944	OMIM:105650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000278	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001249	PMID:10590074	PCS		2/55			P	HPO:skoehler[2010-06-20];HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0003623	PMID:35923690	PCS		1/10			C	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000175	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000494	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000252	PMID:10590074	PCS		1/55			P	HPO:skoehler[2010-06-18];HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0003003	PMID:35923690	PCS		2/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0002671	PMID:35923690	PCS		1/10			P	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001263	PMID:35923690	PCS		1/10			P	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0009777	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0002669	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0030270	PMID:35923690	PCS		8/9			P	HPO:probinson[2015-01-31];HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0008007	PMID:10590074	PCS		2/55			P	HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001896	OMIM:105650	TAS					P	HPO:probinson[2009-02-17]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0008447	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0009778	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001972	PMID:35923690	PCS		8/10			P	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000006	OMIM:105650	IEA					I	HPO:iea[2009-02-17]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000204	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0002984	OMIM:105650	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0002863	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001199	PMID:10590074	PCS		2/55			P	HPO:skoehler[2010-06-18];HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0003577	PMID:35923690	PCS		5/10			C	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000980	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0003298	PMID:35923690	PCS		1/10			P	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001508	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001629	PMID:10590074	PCS		2/55			P	HPO:skoehler[2010-06-18];HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0008475	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000218	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0008437	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000774	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000457	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0004810	OMIM:105650	TAS					P	HPO:probinson[2009-02-17]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001622	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0002697	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001245	PMID:35923690	PCS		7/10			P	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000270	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0011904	PMID:35923690	PCS		6/9			P	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001680	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000470	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000946	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001635	OMIM:105650	IEA					P	HPO:iea[2009-02-17]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0005518	PMID:35923690	PCS		8/9			P	HPO:probinson[2023-06-10]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001511	OMIM:105650	TAS				HP:0012825	P	HPO:probinson[2010-06-20]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001631	PMID:10590074	PCS		2/55			P	HPO:skoehler[2010-06-18];HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001873	PMID:7267232	PCS		12/38			P	HPO:skoehler[2010-06-18];HPO:probinson[2019-07-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000465	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0000347	OMIM:105650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105650	Diamond-Blackfan anemia 1		HP:0001875	PMID:1918400	PCS		HP:0040284			P	HPO:skoehler[2010-06-20];HPO:probinson[2019-07-18]
OMIM:185050	Storage pool platelet disease		HP:0001892	OMIM:185050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:185050	Storage pool platelet disease		HP:0002488	OMIM:185050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:185050	Storage pool platelet disease		HP:0003010	OMIM:185050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:185050	Storage pool platelet disease		HP:0000006	OMIM:185050	IEA					I	HPO:iea[2009-02-17]
OMIM:185050	Storage pool platelet disease		HP:0002863	OMIM:185050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:185050	Storage pool platelet disease		HP:0005537	OMIM:185050	IEA					P	HPO:iea[2009-02-17]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0030799	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0003554	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0002521	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0002188	PMID:28733338	PCS		4/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0006829	PMID:28733338	PCS		5/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0000581	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0000262	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0010602	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0008872	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0001522	PMID:28733338	PCS		5/5			C	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0006610	PMID:28733338	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0003403	PMID:28733338	PCS		1/5			P	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0001166	PMID:28733338	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0011807	PMID:28733338	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0002059	PMID:28733338	PCS		5/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0001561	PMID:28733338	PCS	HP:0011461	2/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0001762	PMID:28733338	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0010516	PMID:28733338	PCS		1/4			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0010851	PMID:28733338	PCS		3/5			P	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0010310	PMID:28733338	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0002803	PMID:28733338	PCS	HP:0003577	3/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0000007	PMID:28733338	PCS					I	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0001558	PMID:28733338	PCS	HP:0011461	5/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0002643	PMID:28733338	PCS	HP:0003623	3/5			P	HPO:probinson[2020-11-29]
OMIM:619036	Myopathy, epilepsy, and progressive cerebral atrophy		HP:0000347	PMID:28733338	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002069	PMID:11359211	PCS		7/7			P	HPO:probinson[2021-07-02]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002123	OMIM:607208	IEA					P	HPO:iea[2009-02-17]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002384	PMID:11359211	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-06-28];HPO:probinson[2021-07-02]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002121	PMID:17347258	PCS	HP:0011463				P	HPO:iea[2009-02-17];HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002121	PMID:11359211	PCS		4/7			P	HPO:probinson[2021-07-02]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0001251	PMID:17347258;PMID:11359211	PCS		15/17			P	HPO:probinson[2021-07-02];HPO:iea[2009-02-17];HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0003593	PMID:11359211	PCS		7/7			C	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0032794	PMID:17347258	PCS	HP:0011463				P	HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0032794	PMID:11359211	PCS		7/7			P	HPO:probinson[2021-07-02]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0001270	OMIM:607208	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0100704	OMIM:607208	TAS					P	HPO:skoehler[2013-01-22]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0001268	OMIM:607208	IEA					P	HPO:iea[2009-02-17]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002059	OMIM:607208	TAS					P	HPO:skoehler[2013-01-22]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0006813	OMIM:607208	IEA					P	HPO:iea[2009-02-17]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002133	OMIM:607208	IEA					P	HPO:iea[2009-02-17]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002376	PMID:17347258	PCS	HP:0011463				P	HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0010819	PMID:17347258	PCS	HP:0011463				P	HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0001263	PMID:17347258	PCS					P	HPO:skoehler[2014-04-04];HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0005484	OMIM:607208	TAS					P	HPO:skoehler[2013-01-22]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0011169	PMID:11359211	PCS		2/7			P	HPO:probinson[2021-07-02]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0007256	PMID:17347258	PCS	HP:0011463				P	HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0200134	PMID:17347258	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0002349	PMID:11359211	PCS		1/7			P	HPO:probinson[2021-07-02]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0000006	PMID:11940708	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-06-28]
OMIM:607208	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)		HP:0020216	PMID:28042998	IEA					P	HPO:probinson[2020-06-28]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000384	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0001377	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003311	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000463	OMIM:272460	IEA					P	HPO:skoehler[2010-06-18]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0001156	OMIM:272460	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000023	OMIM:272460	IEA					P	HPO:skoehler[2019-04-18]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003196	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003691	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000283	OMIM:272460	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0010049	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000518	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0006297	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0006352	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000316	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003307	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002812	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0008456	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003305	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000455	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002656	OMIM:272460	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0009702	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000410	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0001763	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003865	OMIM:272460	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002677	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003521	OMIM:272460	IEA					P	HPO:skoehler[2010-06-18]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0003422	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0007703	PMID:14991055	PCS		HP:0040284			P	HPO:probinson[2017-12-03]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000175	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002650	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0001762	OMIM:272460	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002750	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0001241	PMID:14991055	PCS					P	HPO:probinson[2017-12-03]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000470	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002691	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002091	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000407	OMIM:272460	TAS					P	HPO:skoehler[2014-05-04]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002948	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000107	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000007	PMID:14991055	PCS					I	HPO:probinson[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0004209	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0008368	OMIM:272460	IEA					P	HPO:skoehler[2010-06-18]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0000768	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002007	OMIM:272460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:272460	Spondylocarpotarsal synostosis syndrome		HP:0002644	OMIM:272460	IEA					P	HPO:iea[2009-02-17]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0003577	PMID:30575854	PCS		4/4			C	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0001250	PMID:30575854	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0012196	PMID:30575854	PCS		1/4			P	HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0001252	PMID:30575854	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0002171	PMID:30575854	PCS		1/3			P	HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0000007	PMID:30575854	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0010851	PMID:30575854	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0200134	PMID:30575854	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0002878	PMID:30575854	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0002093	PMID:30575854	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0007305	PMID:30575854	PCS		1/3			P	HPO:probinson[2023-02-12]
OMIM:618328	Epileptic encephalopathy, early infantile, 71		HP:0009879	PMID:30575854	PCS		2/3			P	HPO:probinson[2023-02-12]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0004325	PMID:23832105	PCS		6/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0000252	PMID:23832105	PCS	HP:0003577	6/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0003577	PMID:23832105	PCS		6/6			C	HPO:probinson[2022-08-19]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0002650	PMID:23832105	PCS		1/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0004322	PMID:23832105	PCS		5/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0002750	PMID:23832105	PCS		1/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0000646	PMID:23832105	PCS		1/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0000752	PMID:23832105	PCS		1/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0200065	PMID:23832105	PCS		1/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0000006	PMID:23832105	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:616311	Intellectual developmental disorder, autosomal dominant 33		HP:0001249	PMID:23832105	PCS		6/6			P	HPO:skoehler[2015-09-16];HPO:probinson[2020-07-22]
OMIM:188560	Thyroid hormone plasma membrane transport defect		HP:0008247	OMIM:188560	TAS					P	HPO:skoehler[2009-02-17]
OMIM:188560	Thyroid hormone plasma membrane transport defect		HP:0000006	OMIM:188560	TAS					I	HPO:skoehler[2009-02-17]
OMIM:188560	Thyroid hormone plasma membrane transport defect		HP:0000853	OMIM:188560	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604715	Orthostatic intolerance		HP:0003345	PMID:10684912	PCS		2/2			P	HPO:probinson[2022-06-15]
OMIM:604715	Orthostatic intolerance		HP:0003621	PMID:10684912	PCS		2/2			C	HPO:probinson[2022-06-15]
OMIM:604715	Orthostatic intolerance		HP:0012173	PMID:10684912	PCS		2/2			P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-24];HPO:probinson[2022-06-15]
OMIM:604715	Orthostatic intolerance		HP:0000006	PMID:10684912	PCS					I	HPO:probinson[2013-02-24];HPO:probinson[2020-07-24]
OMIM:145260	Pseudohypoaldosteronism, type II		HP:0002153	OMIM:145260	IEA					P	HPO:iea[2009-02-17]
OMIM:145260	Pseudohypoaldosteronism, type II		HP:0008242	OMIM:145260	TAS					P	HPO:probinson[2012-07-17]
OMIM:145260	Pseudohypoaldosteronism, type II		HP:0000822	OMIM:145260	IEA					P	HPO:iea[2009-02-17]
OMIM:145260	Pseudohypoaldosteronism, type II		HP:0001995	OMIM:145260	IEA					P	HPO:iea[2009-02-17]
OMIM:145260	Pseudohypoaldosteronism, type II		HP:0007215	OMIM:145260	IEA					P	HPO:iea[2009-02-17]
OMIM:145260	Pseudohypoaldosteronism, type II		HP:0000006	OMIM:145260	IEA					I	HPO:iea[2009-02-17]
OMIM:617769	Spinocerebellar ataxia 45		HP:0003596	PMID:29053796	PCS		1/1			C	HPO:probinson[2023-02-20]
OMIM:617769	Spinocerebellar ataxia 45		HP:0001272	PMID:29053796	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617769	Spinocerebellar ataxia 45		HP:0001260	PMID:29053796	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617769	Spinocerebellar ataxia 45		HP:0002066	PMID:29053796	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617769	Spinocerebellar ataxia 45		HP:0002070	PMID:29053796	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617769	Spinocerebellar ataxia 45		HP:0000006	PMID:29053796	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-02-20]
OMIM:617769	Spinocerebellar ataxia 45		HP:0003677	PMID:29053796	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617769	Spinocerebellar ataxia 45		HP:0010545	PMID:29053796	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0001561	PMID:21856041	PCS	HP:0011461	9/9			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0002099	PMID:21856041	PCS		6/23			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0025092	PMID:21856041	PCS		10/10			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0012768	PMID:21856041	PCS		17/17			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0002293	PMID:21856041	PCS		2/23			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0003193	PMID:21856041	PCS		6/23			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0011971	PMID:21856041	PCS					P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0500093	PMID:21856041	PCS		6/23			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0025724	PMID:21856041	PCS		23/23			P	HPO:probinson[2022-02-03]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0000007	PMID:21856041	PCS					I	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0000953	PMID:21856041	PCS					P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0001019	PMID:21856041	PCS	HP:0003577	23/23			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0000989	PMID:21856041	PCS		23/23			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0007502	PMID:21856041	PCS		23/23			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0007503	PMID:21856041	PCS		23/23			P	HPO:probinson[2021-08-16]
OMIM:608649	Ichthyosis prematurity syndrome		HP:0001622	PMID:21856041	PCS	HP:0003577	23/23			P	HPO:probinson[2021-08-16]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0001254	OMIM:610006	IEA					P	HPO:iea[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0000252	OMIM:610006	IEA					P	HPO:iea[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0002045	OMIM:610006	IEA					P	HPO:iea[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0001250	OMIM:610006	IEA					P	HPO:iea[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0001252	PMID:11013134	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0001263	OMIM:610006	TAS					P	HPO:probinson[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0003593	OMIM:610006	IEA					C	HPO:iea[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0001270	PMID:11013134	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0033220	PMID:11013134	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0011463	PMID:11013134	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0001943	OMIM:610006	IEA					P	HPO:iea[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0000007	PMID:11013134	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0005949	OMIM:610006	IEA					P	HPO:iea[2009-02-17]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0003700	PMID:11013134	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:610006	2-Methylbutyryl-Coa dehydrogenase deficiency		HP:0000577	OMIM:610006	IEA					P	HPO:iea[2009-02-17]
OMIM:606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0003235	OMIM:606664	IEA					P	HPO:iea[2009-02-17]
OMIM:606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0002240	OMIM:606664	IEA					P	HPO:iea[2009-02-17]
OMIM:606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0000007	OMIM:606664	IEA					I	HPO:iea[2009-02-17]
OMIM:606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0002910	OMIM:606664	IEA					P	HPO:iea[2009-02-17]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003236	PMID:23352259	PCS		1/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003198	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003551	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003394	PMID:23352259	PCS		1/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003391	PMID:23352259	PCS		2/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0000716	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0011462	PMID:23352259	PCS		2/4			C	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003749	PMID:23352259	PCS		3/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003307	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003547	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0001324	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0000597	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003326	PMID:23352259	PCS		1/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003689	PMID:23352259	PCS		4/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003700	PMID:23352259	PCS		1/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0002875	PMID:23352259	PCS		2/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003546	PMID:23352259	PCS					P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0002870	PMID:23352259	PCS		1/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0001288	PMID:23352259	PCS		4/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0000590	PMID:23352259	PCS		4/4			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0004673	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003581	PMID:23352259	PCS		2/4			C	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0002094	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0000508	PMID:23352259	PCS		3/4		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0002527	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0001533	PMID:23352259	PCS		1/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0003677	PMID:23352259	PCS					C	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0000006	PMID:23352259	PCS					I	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-05]
OMIM:615156	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal dominant, 6		HP:0001655	PMID:23352259	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0001894	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0025043	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0003496	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0003073	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0012649	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0001903	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0002716	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0100727	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0001945	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0001824	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0001744	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0002039	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0003565	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0002014	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0002113	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0005661	OMIM:209950	IEA					P	HPO:iea[2009-02-17]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0030166	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0002090	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0025427	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0000007	PMID:7815885	PCS					I	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0002923	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0001433	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0003237	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0008802	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:209950	Immunodeficiency 27A, mycobacteriosis, AR		HP:0001974	PMID:7815885	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:112310	Boomerang dysplasia		HP:0003510	OMIM:112310	TAS					P	HPO:probinson[2009-02-17]
OMIM:112310	Boomerang dysplasia		HP:0000431	OMIM:112310	IEA					P	HPO:iea[2009-02-17]
OMIM:112310	Boomerang dysplasia		HP:0005104	OMIM:112310	TAS					P	HPO:probinson[2012-06-10]
OMIM:112310	Boomerang dysplasia		HP:0000430	OMIM:112310	TAS					P	HPO:probinson[2012-06-10]
OMIM:112310	Boomerang dysplasia		HP:0002990	OMIM:112310	TAS					P	HPO:probinson[2012-06-10]
OMIM:112310	Boomerang dysplasia		HP:0003811	OMIM:112310	TAS					C	HPO:probinson[2009-02-17]
OMIM:112310	Boomerang dysplasia		HP:0000006	OMIM:112310	IEA					I	HPO:iea[2009-02-17]
OMIM:112310	Boomerang dysplasia		HP:0003974	OMIM:112310	TAS					P	HPO:probinson[2009-02-17]
OMIM:112310	Boomerang dysplasia		HP:0008824	OMIM:112310	IEA					P	HPO:iea[2009-02-17]
OMIM:233400	Perrault syndrome 1		HP:0001265	OMIM:233400	TAS		HP:0040283			P	HPO:skoehler[2012-12-03]
OMIM:233400	Perrault syndrome 1		HP:0001264	OMIM:233400	TAS		HP:0040283			P	HPO:skoehler[2012-12-03]
OMIM:233400	Perrault syndrome 1		HP:0002650	OMIM:233400	TAS					P	HPO:skoehler[2012-12-03]
OMIM:233400	Perrault syndrome 1		HP:0001762	OMIM:233400	IEA					P	HPO:iea[2009-02-17]
OMIM:233400	Perrault syndrome 1		HP:0000133	PMID:20673864	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0001761	OMIM:233400	TAS					P	HPO:skoehler[2012-12-03]
OMIM:233400	Perrault syndrome 1		HP:0004322	PMID:20673864	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0001272	PMID:20673864	PCS		1/2			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0001260	PMID:20673864	PCS		1/2			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0002066	OMIM:233400	IEA					P	HPO:iea[2009-02-17]
OMIM:233400	Perrault syndrome 1		HP:0001284	OMIM:233400	TAS		HP:0040283			P	HPO:skoehler[2012-12-03]
OMIM:233400	Perrault syndrome 1		HP:0001251	PMID:20673864	PCS		1/2			P	HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0001270	OMIM:233400	TAS		HP:0040283			P	HPO:skoehler[2012-12-03]
OMIM:233400	Perrault syndrome 1		HP:0002080	PMID:20673864	PCS		1/2			P	HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0000939	OMIM:233400	IEA					P	HPO:iea[2009-02-17]
OMIM:233400	Perrault syndrome 1		HP:0000837	OMIM:233400	IEA					P	HPO:iea[2009-02-17]
OMIM:233400	Perrault syndrome 1		HP:0000639	OMIM:233400	IEA					P	HPO:iea[2009-02-17]
OMIM:233400	Perrault syndrome 1		HP:0007141	PMID:20673864	PCS		2/2			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0000407	PMID:20673864	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0000007	PMID:20673864	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:233400	Perrault syndrome 1		HP:0000218	OMIM:233400	TAS					P	HPO:skoehler[2012-12-03]
OMIM:233400	Perrault syndrome 1		HP:0007941	OMIM:233400	IEA					P	HPO:iea[2009-02-17]
OMIM:233400	Perrault syndrome 1		HP:0000786	OMIM:233400	IEA					P	HPO:iea[2009-02-17]
OMIM:300960	Mend syndrome		HP:0001650	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0001276	OMIM:300960	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300960	Mend syndrome		HP:0000582	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0001134	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0004322	OMIM:300960	TAS					P	HPO:skoehler[2015-10-05]
OMIM:300960	Mend syndrome		HP:0001250	OMIM:300960	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0001252	OMIM:300960	TAS		1/1			P	HPO:skoehler[2015-10-05]
OMIM:300960	Mend syndrome		HP:0010442	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0005590	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000518	OMIM:300960	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300960	Mend syndrome		HP:0001508	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0010055	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000319	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0001845	OMIM:300960	TAS		1/1			P	HPO:skoehler[2015-10-05]
OMIM:300960	Mend syndrome		HP:0000414	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0001305	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0000238	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0100807	OMIM:300960	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0007663	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000218	OMIM:300960	TAS		1/1			P	HPO:skoehler[2015-10-05]
OMIM:300960	Mend syndrome		HP:0004736	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000752	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0001104	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0005989	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0001249	OMIM:300960	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300960	Mend syndrome		HP:0000358	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000237	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0008936	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000396	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000472	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0001344	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0001263	OMIM:300960	TAS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:300960	Mend syndrome		HP:0004691	OMIM:300960	TAS					P	HPO:skoehler[2015-10-05]
OMIM:300960	Mend syndrome		HP:0045025	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0011800	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0010557	OMIM:300960	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0008064	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0002808	OMIM:300960	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300960	Mend syndrome		HP:0000308	OMIM:300960	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0001419	PMID:12503101	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000426	OMIM:300960	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:300960	Mend syndrome		HP:0000565	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000960	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:300960	Mend syndrome		HP:0000028	OMIM:300960	TAS					P	HPO:skoehler[2015-10-05]
OMIM:300960	Mend syndrome		HP:0000369	OMIM:300960	TAS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:300960	Mend syndrome		HP:0000347	PMID:12503101	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0008936	PMID:25817015	PCS		2/3			P	HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0002059	PMID:25817015	PCS		3/3		HP:0003676	P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0003577	PMID:25817015;OMIM:616339	PCS		11/13			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0000252	PMID:25817015	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0004322	PMID:25817015	PCS		2/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0002310	PMID:25817015	PCS		3/3			P	HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0002451	PMID:25817015	PCS		3/3			P	HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0001263	PMID:25817015	PCS		3/3		HP:0012829	P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0001284	PMID:25817015	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0003593	PMID:25817015	PCS		2/3			C	HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0002072	PMID:25817015	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0032794	PMID:25817015	PCS		3/3			P	HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0000639	PMID:25817015	PCS		1/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0001508	PMID:25817015	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0001838	PMID:25817015	PCS	HP:0003577	3/3			P	HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0002827	PMID:25817015	PCS	HP:0003577	2/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0009830	PMID:25817015	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0000007	PMID:25817015	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0200134	PMID:25817015	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0003429	PMID:25817015	PCS		2/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0001511	PMID:25817015	PCS		2/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0001257	PMID:25817015	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:616339	Epileptic encephalopathy, early infantile, 29		HP:0000643	PMID:25817015	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-24]
OMIM:109730	Aortic valve disease 1		HP:0001650	PMID:16025100	PCS		7/14			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0001629	PMID:16025100	PCS		2/14			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0001719	PMID:16025100	PCS	HP:0003577	1/14			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0001718	PMID:16025100	PCS		1/14			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0011560	PMID:16025100	PCS		1/14			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0001647	PMID:16025100	PCS	HP:0003577	9/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0001636	PMID:16025100	PCS		1/14			P	HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0004380	PMID:16025100	PCS		9/10			P	HPO:probinson[2022-12-02]
OMIM:109730	Aortic valve disease 1		HP:0000006	PMID:16025100	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2022-12-02]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0005942	OMIM:265120	IEA					P	HPO:skoehler[2012-07-16]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0006517	PMID:11207353;PMID:10378403	PCS		5/5			P	HPO:probinson[2021-05-05];HPO:skoehler[2014-06-24];HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0025179	PMID:15819986;PMID:10378403	PCS		12/15			P	HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0002094	OMIM:265120	TAS					P	HPO:probinson[2012-07-16]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0032981	PMID:15819986	PCS					P	HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0002092	PMID:10378403	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0030879	PMID:11373919	PCS		2/3			P	HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0001508	OMIM:265120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0033186	PMID:10378403	PCS		1/3			P	HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0001217	OMIM:265120	TAS					P	HPO:probinson[2009-02-17]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0000007	PMID:8163685	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0002878	OMIM:265120	TAS	HP:0003623				P	HPO:skoehler[2014-06-24]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0000961	OMIM:265120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0001522	PMID:10378403;PMID:15218289	PCS		12/15			C	HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0003811	PMID:10378403	PCS		3/5			C	HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0002789	OMIM:265120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0002104	PMID:10378403	PCS	HP:0003623	3/5			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0002643	PMID:11207353	PCS	HP:0003623				P	HPO:probinson[2021-05-05]
OMIM:265120	Surfactant metabolism dysfunction, pulmonary, 1		HP:0003623	PMID:10378403	PCS		5/5			C	HPO:probinson[2021-05-05]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0000121	PMID:30388404	PCS		0/3			P	HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0005567	PMID:30388404	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0002133	PMID:30388404	PCS		2/3		HP:0031796	P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0002197	PMID:30388404	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0001250	PMID:30388404	PCS		3/3			P	HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0001263	PMID:30388404	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0003593	PMID:30388404	PCS		2/3			C	HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0012169	PMID:30388404	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0002917	PMID:30388404	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0000128	PMID:30388404	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0002900	PMID:30388404	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0002119	PMID:30388404	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0000752	PMID:30388404	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0000103	PMID:30388404	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0000006	PMID:30388404	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-06]
OMIM:618314	Hypomagnesemia, seizures, and impaired intellectual development 2		HP:0003623	PMID:30388404	PCS		1/3			C	HPO:probinson[2022-10-06]
OMIM:617027	Hyperaldosteronism, familial, type IV		HP:0003621	PMID:25907736	PCS		3/5			C	HPO:probinson[2022-11-05]
OMIM:617027	Hyperaldosteronism, familial, type IV		HP:0000859	PMID:25907736	PCS		5/5			P	HPO:probinson[2022-11-05];HPO:probinson[2022-11-05]
OMIM:617027	Hyperaldosteronism, familial, type IV		HP:0011463	PMID:25907736	PCS		1/5			C	HPO:probinson[2022-11-05]
OMIM:617027	Hyperaldosteronism, familial, type IV		HP:0003593	PMID:25907736	PCS		1/5			C	HPO:probinson[2022-11-05]
OMIM:617027	Hyperaldosteronism, familial, type IV		HP:0000822	PMID:25907736	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-05]
OMIM:617027	Hyperaldosteronism, familial, type IV		HP:0000006	PMID:25907736	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-05]
OMIM:617027	Hyperaldosteronism, familial, type IV		HP:6000318	PMID:25907736	PCS		5/5			P	HPO:probinson[2024-02-27]
OMIM:228020	Fascial dystrophy, congenital		HP:0001376	OMIM:228020	IEA					P	HPO:iea[2009-02-17]
OMIM:228020	Fascial dystrophy, congenital		HP:0005750	OMIM:228020	IEA					P	HPO:iea[2009-02-17]
OMIM:228020	Fascial dystrophy, congenital		HP:0002086	OMIM:228020	IEA					P	HPO:iea[2009-02-17]
OMIM:228020	Fascial dystrophy, congenital		HP:0000007	OMIM:228020	IEA					I	HPO:iea[2009-02-17]
OMIM:228020	Fascial dystrophy, congenital		HP:0000765	OMIM:228020	IEA					P	HPO:iea[2009-02-17]
OMIM:228020	Fascial dystrophy, congenital		HP:0000951	OMIM:228020	IEA					P	HPO:iea[2009-02-17]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001396	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001399	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000662	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0005257	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0004322	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001156	OMIM:615630	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001591	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001395	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0002240	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0012622	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001629	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0010230	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000657	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000238	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0002119	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0002857	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000773	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001744	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001249	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001320	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0003026	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001162	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000090	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0040270	OMIM:615630	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000546	OMIM:615630	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000007	OMIM:615630	TAS					I	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0000202	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0006644	OMIM:615630	TAS					P	HPO:skoehler[2015-01-21]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001513	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		HP:0001952	OMIM:615630	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0031318	PMID:16236538;PMID:16712796	PCS		2/2			P	HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0003596	PMID:16236538	PCS		1/1			C	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0031319	PMID:16236538;PMID:16712796	PCS		2/2			P	HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0003584	PMID:16712796	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0034313	PMID:16236538	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0031992	PMID:16236538	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0002092	PMID:16236538	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0001639	PMID:16236538;PMID:16712796	PCS		2/2			P	HPO:probinson[2022-07-04];HPO:skoehler[2013-01-09];HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0001635	PMID:16236538;PMID:16712796	PCS		2/2			P	HPO:probinson[2022-07-04];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0006685	PMID:16236538	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0000006	PMID:16236538	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0032092	PMID:16236538;PMID:16712796	PCS		2/2			P	HPO:probinson[2022-07-04]
OMIM:613255	Cardiomyopathy, familial hypertrophic, 15		HP:0002875	PMID:16236538;PMID:16712796	PCS		2/2			P	HPO:probinson[2022-07-04]
OMIM:180100	Retinitis pigmentosa 1		HP:0001133	PMID:10391211	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0007737	PMID:10391211	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0003621	PMID:32565670	PCS		8/19			C	HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0000662	PMID:10391211;PMID:32565670	PCS		26/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01];HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0011463	PMID:32565670	PCS		3/19			C	HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0011462	PMID:32565670	PCS		8/19			C	HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0000007	PMID:10391211	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0007663	PMID:32565670	PCS		16/18			P	HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0000510	PMID:10391211	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0007688	OMIM:180100	IEA					P	HPO:iea[2009-02-17]
OMIM:180100	Retinitis pigmentosa 1		HP:0000543	PMID:10391211	PCS		1/1			P	HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0007843	PMID:10391211	PCS		10/10			P	HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0000575	PMID:32565670	PCS		5/18			P	HPO:probinson[2022-09-01]
OMIM:180100	Retinitis pigmentosa 1		HP:0000006	OMIM:180100	TAS					I	HPO:skoehler[2015-12-30]
OMIM:180100	Retinitis pigmentosa 1		HP:0000545	OMIM:180100	TAS				HP:0012826	P	HPO:skoehler[2017-07-13]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0002157	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000099	OMIM:104200	IEA					P	HPO:skoehler[2012-10-11]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000121	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0003774	OMIM:104200	TAS					P	HPO:skoehler[2012-11-26]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0003774	PMID:11044206	PCS	HP:0003581	2/7			P	HPO:probinson[2022-10-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0003676	OMIM:104200	IEA					C	HPO:skoehler[2012-10-11]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000123	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000365	PMID:11044206	PCS		1/7			P	HPO:probinson[2022-10-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0001134	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000100	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000083	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0030034	OMIM:104200	TAS					P	HPO:skoehler[2014-09-21]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000790	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0001142	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000093	PMID:11044206	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000407	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0002907	PMID:11044206	PCS		7/7			P	HPO:probinson[2022-10-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000822	PMID:11044206	PCS					P	HPO:skoehler[2012-10-11];HPO:probinson[2022-10-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000006	PMID:11044206	PCS					I	HPO:skoehler[2012-10-11];HPO:probinson[2022-10-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0002148	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0000545	OMIM:104200	IEA					P	HPO:iea[2009-02-17]
OMIM:104200	Alport syndrome 3, autosomal dominant		HP:0004722	OMIM:104200	IEA					P	HPO:skoehler[2012-10-11]
OMIM:610984	Complement factor I deficiency		HP:0000099	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0000010	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0003621	OMIM:610984	IEA					C	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0005369	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0006946	PMID:8613545	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0005356	PMID:8613545	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0005366	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0005421	PMID:8613545	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0000083	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0005376	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0001581	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:610984	Complement factor I deficiency		HP:0003593	PMID:8613545	IEA		1/2			C	HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0003095	PMID:8613545	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0005381	PMID:8613545	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0011108	PMID:8613545	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0012330	OMIM:610984	TAS					P	HPO:skoehler[2013-09-17]
OMIM:610984	Complement factor I deficiency		HP:0011463	PMID:8613545	PCS		1/2			C	HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0000007	PMID:8613545	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0000403	PMID:8613545	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0005416	PMID:8613545	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610984	Complement factor I deficiency		HP:0002633	OMIM:610984	IEA					P	HPO:iea[2009-02-17]
OMIM:149300	Koilonychia, hereditary		HP:0001598	OMIM:149300	IEA					P	HPO:iea[2009-02-17]
OMIM:149300	Koilonychia, hereditary		HP:0000006	OMIM:149300	IEA					I	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001771	PMID:17998446	PCS		2/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0009937	PMID:12624138	PCS		1/1			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0003676	OMIM:252940	IEA					C	HPO:skoehler[2010-06-19]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000365	PMID:17998446	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0010769	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0004322	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001250	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0003593	PMID:17998446	PCS		1/3			C	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000280	PMID:17998446;PMID:12624138	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0011463	PMID:17998446;PMID:12624138	PCS		3/4			C	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000718	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0011220	PMID:17998446	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0012471	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000316	PMID:12624138	PCS		1/1			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0003309	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000711	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000713	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002656	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000752	PMID:17998446	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000158	PMID:12624138	PCS		1/1			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001169	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001007	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001249	PMID:17998446	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001385	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001344	OMIM:252940	TAS					P	HPO:skoehler[2014-11-26]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000574	PMID:17998446	PCS		2/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001387	OMIM:252940	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000490	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001260	PMID:17998446	PCS		1/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001263	PMID:17998446	PCS		3/3			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0031354	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0033454	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:4000198	OMIM:252940	TAS					P	HPO:probinson[2024-01-06]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000007	PMID:12573255	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000403	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002307	PMID:17998446	PCS		2/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002788	PMID:17998446	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002987	PMID:17998446	PCS		2/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001653	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002943	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000369	PMID:17998446	PCS		1/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000187	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0003653	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000662	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000463	PMID:17998446	PCS		1/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000023	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001272	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0031849	PMID:17998446	PCS		2/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001670	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002240	PMID:17998446	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0010865	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001507	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0008479	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000256	PMID:12624138	PCS		1/1			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000179	OMIM:252940	IEA					P	HPO:skoehler[2010-06-18]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001348	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002159	PMID:17998446;PMID:12624138	PCS		4/4			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10];HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001744	PMID:17998446	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002014	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000154	PMID:17998446	PCS		1/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002015	PMID:17998446	PCS		2/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000750	PMID:17998446	PCS		3/3			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001288	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0001761	PMID:17998446	PCS		2/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000470	PMID:17998446	PCS		2/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0005280	PMID:17998446;PMID:12624138	PCS		3/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000943	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000505	PMID:17998446	PCS		1/3			P	HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002208	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000900	OMIM:252940	IEA					P	HPO:iea[2009-02-17]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0002007	PMID:12624138	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:252940	Mucopolysaccharidosis, type IIID		HP:0000664	PMID:17998446	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:156220	Meralgia paraesthetica, familial		HP:0000707	OMIM:156220	IEA					P	HPO:iea[2009-02-17]
OMIM:156220	Meralgia paraesthetica, familial		HP:0000006	OMIM:156220	IEA					I	HPO:iea[2009-02-17]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0003621	PMID:30471717	PCS		2/4			C	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0002257	PMID:30471717	PCS		4/4			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0003577	PMID:30471717	PCS		1/4			C	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0001696	PMID:30471717;PMID:30471718	PCS		7/9			P	HPO:probinson[2022-03-07];HPO:skoehler[2019-02-15];HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0033036	PMID:30471717	PCS		1/4			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0033158	PMID:30471717	PCS		1/4			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0012735	PMID:30471717	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0011109	PMID:30471717	PCS		4/4			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0031854	PMID:30471718	PCS		1/5			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0011579	PMID:30471717	PCS		1/4			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0012256	PMID:30471718	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0011463	PMID:30471717	PCS		1/4			C	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0011540	PMID:30471717	PCS		1/4			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0011671	PMID:30471718	PCS		1/5			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0012020	PMID:30471718	PCS		1/5			P	HPO:probinson[2022-03-07];HPO:probinson[2022-07-10]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0032342	PMID:30471717	PCS		1/4			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0000789	PMID:30471717	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0000007	PMID:30471717	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0006695	PMID:30471718	PCS		1/5			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0001643	PMID:30471718	PCS		1/5			P	HPO:probinson[2022-03-07]
OMIM:618300	Ciliary dyskinesia, primary, 40		HP:0000027	PMID:30471717	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-07]
OMIM:309950	Muscular dystrophy, hemizygous Lethal type		HP:0006785	OMIM:309950	TAS					P	HPO:probinson[2009-02-17]
OMIM:309950	Muscular dystrophy, hemizygous Lethal type		HP:0001423	OMIM:309950	TAS			MALE		I	HPO:nvasilevsky[2019-03-11]
OMIM:309950	Muscular dystrophy, hemizygous Lethal type		HP:0000006	OMIM:309950	TAS			FEMALE		I	HPO:nvasilevsky[2019-03-11]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000286	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000582	PMID:28942966	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0004322	PMID:28942966	PCS		4/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000160	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001290	PMID:28942966	PCS		5/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0012745	PMID:28942966	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001270	PMID:28942966	PCS		8/10			P	HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0010055	PMID:28942966	PCS		5/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000316	PMID:28942966	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001845	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0020045	PMID:28942966	PCS		1/10			P	HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000219	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000455	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001763	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001249	PMID:28942966	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000252	PMID:28942966	PCS		7/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000750	PMID:28942966	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001263	PMID:28942966	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0011229	PMID:28942966	PCS		2/10			P	HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0033142	PMID:28942966	PCS		2/10			P	HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000448	PMID:28942966	PCS		7/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0004209	PMID:28942966	PCS		3/10			P	HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001852	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0200055	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0002500	PMID:28942966	PCS		3/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000006	PMID:28942966	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0000347	PMID:28942966	PCS		3/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-13]
OMIM:617755	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies		HP:0001238	PMID:28942966	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:184400	Sprengel deformity		HP:0004632	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0002650	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0003298	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0002937	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0000912	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0008952	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0008984	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0003745	OMIM:184400	IEA					I	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0006655	OMIM:184400	IEA					P	HPO:iea[2009-02-17]
OMIM:184400	Sprengel deformity		HP:0000006	OMIM:184400	IEA					I	HPO:iea[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002168	OMIM:606658	TAS					P	HPO:skoehler[2010-06-18]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002345	OMIM:606658	IEA					P	HPO:iea[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0007979	OMIM:606658	TAS					P	HPO:skoehler[2010-06-18]
OMIM:606658	Spinocerebellar ataxia 15		HP:0000640	PMID:21367767;PMID:37154409	PCS		9/13			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0003596	PMID:21367767;PMID:37154409	PCS		8/14			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0001272	PMID:37154409	PCS		4/4			P	HPO:iea[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0031629	PMID:37154409	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002066	PMID:37154409	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002080	PMID:21367767	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0000639	PMID:37154409	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0011462	PMID:21367767	PCS		3/9			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0008278	PMID:21367767	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0001249	PMID:37154409	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0006855	PMID:21367767	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0001347	OMIM:606658	IEA					P	HPO:iea[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002136	PMID:37154409	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002015	PMID:21367767	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0000571	PMID:21367767	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0003621	OMIM:606658	TAS					C	HPO:skoehler[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002078	PMID:37154409	PCS		5/5			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0003487	PMID:21367767	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0001288	PMID:21367767;PMID:37154409	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0001260	PMID:21367767;PMID:37154409	PCS		8/14			P	ORCID:0000-0002-0736-9199[2024-07-17];HPO:iea[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0003584	PMID:21367767;PMID:37154409	PCS		3/14			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0003581	OMIM:606658	TAS					C	HPO:skoehler[2013-03-10]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002174	PMID:21367767	PCS		7/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002072	PMID:37154409	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0100021	PMID:21367767;PMID:37154409	PCS		0/14			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002070	OMIM:606658	TAS					P	HPO:skoehler[2010-06-18]
OMIM:606658	Spinocerebellar ataxia 15		HP:0012758	PMID:21367767;PMID:37154409	PCS		0/14			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0100660	PMID:37154409	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0007772	OMIM:606658	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606658	Spinocerebellar ataxia 15		HP:0002406	PMID:21367767;PMID:37154409	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0000641	OMIM:606658	TAS					P	HPO:skoehler[2010-06-18]
OMIM:606658	Spinocerebellar ataxia 15		HP:0001257	PMID:21367767	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0000006	PMID:37154409	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0007338	PMID:21367767	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0003677	OMIM:606658	IEA					C	HPO:iea[2009-02-17]
OMIM:606658	Spinocerebellar ataxia 15		HP:0001337	PMID:37154409	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:100700	Achard syndrome		HP:0001166	OMIM:100700	IEA					P	HPO:iea[2009-02-17]
OMIM:100700	Achard syndrome		HP:0001382	OMIM:100700	TAS					P	HPO:probinson[2009-02-17]
OMIM:100700	Achard syndrome		HP:0002682	OMIM:100700	IEA					P	HPO:iea[2009-02-17]
OMIM:100700	Achard syndrome		HP:0000006	OMIM:100700	IEA					I	HPO:iea[2009-02-17]
OMIM:100700	Achard syndrome		HP:0000248	OMIM:100700	IEA					P	HPO:iea[2009-02-17]
OMIM:100700	Achard syndrome		HP:0000347	OMIM:100700	IEA					P	HPO:iea[2009-02-17]
OMIM:603720	Deafness, autosomal recessive 16		HP:0000407	PMID:11687802	PCS		HP:0040280			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-19]
OMIM:603720	Deafness, autosomal recessive 16		HP:0000007	PMID:11687802	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-07-19]
OMIM:135750	Laurin-Sandrow syndrome		HP:0001199	OMIM:135750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135750	Laurin-Sandrow syndrome		HP:0001773	OMIM:135750	TAS					P	HPO:probinson[2013-04-08]
OMIM:135750	Laurin-Sandrow syndrome		HP:0000430	OMIM:135750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135750	Laurin-Sandrow syndrome		HP:0000271	OMIM:135750	IEA					P	HPO:iea[2009-02-17]
OMIM:135750	Laurin-Sandrow syndrome		HP:0001161	OMIM:135750	IEA					P	HPO:iea[2009-02-17]
OMIM:135750	Laurin-Sandrow syndrome		HP:0006443	OMIM:135750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135750	Laurin-Sandrow syndrome		HP:0001769	OMIM:135750	TAS					P	HPO:probinson[2013-04-08]
OMIM:135750	Laurin-Sandrow syndrome		HP:0009556	OMIM:135750	TAS					P	HPO:skoehler[2013-10-22]
OMIM:135750	Laurin-Sandrow syndrome		HP:0001159	OMIM:135750	IEA					P	HPO:iea[2009-02-17]
OMIM:135750	Laurin-Sandrow syndrome		HP:0010503	OMIM:135750	IEA					P	HPO:skoehler[2010-06-18]
OMIM:135750	Laurin-Sandrow syndrome		HP:0000006	OMIM:135750	IEA					I	HPO:iea[2009-02-17]
OMIM:135750	Laurin-Sandrow syndrome		HP:0003974	OMIM:135750	IEA					P	HPO:iea[2009-02-17]
OMIM:619793	Restrictive dermopathy 2		HP:0003577	PMID:15317753	PCS		1/2			C	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0002035	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0002692	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0011968	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0002098	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0002020	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0001072	PMID:15317753	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0006391	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0100324	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0000308	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0011461	PMID:15317753	PCS		1/2			C	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0001558	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0025116	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0001511	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0000961	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0000444	PMID:15317753	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0000894	PMID:15317753	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0000520	PMID:15317753	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:619793	Restrictive dermopathy 2		HP:0000006	PMID:15317753	PCS					I	HPO:probinson[2022-05-28]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0001265	OMIM:158580	IEA					P	HPO:iea[2009-02-17]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0030205	PMID:23141292	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0003621	PMID:23141292	PCS					C	HPO:probinson[2022-09-04]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0001288	OMIM:158580	TAS					P	HPO:skoehler[2013-06-05]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0001761	OMIM:158580	TAS					P	HPO:skoehler[2013-06-05]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0003693	OMIM:158580	TAS					P	HPO:skoehler[2009-02-17]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0002460	OMIM:158580	TAS					P	HPO:skoehler[2009-02-17]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0040131	PMID:23141292	PCS		0/14			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-08]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0009830	OMIM:158580	TAS					P	HPO:skoehler[2015-01-21]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0001605	OMIM:158580	TAS					P	HPO:skoehler[2015-01-21]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0001604	OMIM:158580	IEA					P	HPO:iea[2009-02-17]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0000006	PMID:23141292	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0003677	OMIM:158580	IEA					C	HPO:iea[2009-02-17]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0001337	OMIM:158580	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:158580	Neuronopathy, distal hereditary motor, type VIIA		HP:0003403	PMID:23141292	PCS		0/2			P	HPO:probinson[2024-03-08]
OMIM:178650	Pulmonic stenosis, atrial septal defect, and unique electrocardiographicabnormalities		HP:0003115	OMIM:178650	TAS					P	HPO:probinson[2013-03-12]
OMIM:178650	Pulmonic stenosis, atrial septal defect, and unique electrocardiographicabnormalities		HP:0001684	OMIM:178650	TAS					P	HPO:probinson[2013-03-12]
OMIM:178650	Pulmonic stenosis, atrial septal defect, and unique electrocardiographicabnormalities		HP:0001642	OMIM:178650	TAS					P	HPO:probinson[2009-02-17]
OMIM:178650	Pulmonic stenosis, atrial septal defect, and unique electrocardiographicabnormalities		HP:0000006	OMIM:178650	TAS					I	HPO:probinson[2009-02-17]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0033606	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0011919	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0001058	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0000089	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0003593	PMID:32325141	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0032299	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0034284	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0012311	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0001903	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0100806	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0200043	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0009789	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0000230	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0003261	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0002090	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0011108	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0032128	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0011107	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0011110	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0032154	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0000403	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0001873	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0000006	PMID:32325141	PCS					I	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0002149	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620674	Neutropenia, severe congenital, 11, autosomal dominant		HP:0001875	PMID:32325141	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0002553	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0000252	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0000750	PMID:21498477;PMID:34599609	PCS		9/9			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0000486	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0004322	PMID:21498477;PMID:34599609	PCS		9/9			P	HPO:probinson[2022-03-11];HPO:skoehler[2014-07-11];HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0031936	PMID:34599609	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0001263	PMID:21498477	PCS		7/7			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0001252	PMID:34599609	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0003593	PMID:21498477	PCS		7/7			C	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0010862	PMID:21498477	PCS		7/7			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0012736	PMID:34599609	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0034042	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0011220	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0000007	PMID:21498477	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0100716	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0000219	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0000455	PMID:34599609	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0001257	PMID:21498477	PCS		1/7			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0001249	PMID:21498477	PCS		7/7			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0000369	PMID:34599609	PCS		1/2			P	HPO:probinson[2022-03-11]
OMIM:615817	Intellectual developmental disorder, autosomal recessive 43		HP:0003623	PMID:34599609	PCS		2/2			C	HPO:probinson[2022-03-11]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001298	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000341	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000486	PMID:29307788	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000540	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002120	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001250	PMID:29307788	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0003396	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0003196	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002020	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0003593	PMID:29307788	PCS		2/2			C	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0012448	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002280	PMID:29307788	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000639	PMID:29307788	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0100704	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000817	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000414	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000637	PMID:29307788	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000219	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002119	PMID:29307788	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000218	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0009765	PMID:29307788	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002019	PMID:29307788	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001347	PMID:29307788	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0008936	PMID:29307788	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002553	PMID:29307788	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002751	PMID:29307788	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000253	OMIM:615803	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000252	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001344	PMID:29307788	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000431	PMID:29307788	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002079	PMID:29307788	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000430	PMID:29307788	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0011968	PMID:29307788	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001263	PMID:29307788	PCS		2/2		HP:0012829	P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000470	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001182	PMID:29307788	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0034295	PMID:29307788	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0002509	PMID:29307788	PCS		4/4			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000007	PMID:29307788	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000527	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000565	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000664	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001510	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000520	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0001257	PMID:29307788	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-30]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000028	OMIM:615803	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0009879	OMIM:615803	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615803	Pontocerebellar hypoplasia, type 10		HP:0000687	PMID:29307788	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:202150	Adrenal hypoplasia, congenital, with absent pituitary luteinizinghormone		HP:0000054	PMID:2906226	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:202150	Adrenal hypoplasia, congenital, with absent pituitary luteinizinghormone		HP:0030344	PMID:2906226	PCS		3/3			P	HPO:probinson[2022-07-03]
OMIM:202150	Adrenal hypoplasia, congenital, with absent pituitary luteinizinghormone		HP:0008244	PMID:2906226	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:202150	Adrenal hypoplasia, congenital, with absent pituitary luteinizinghormone		HP:0000007	PMID:2906226	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:202150	Adrenal hypoplasia, congenital, with absent pituitary luteinizinghormone		HP:0000028	PMID:2906226	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:202150	Adrenal hypoplasia, congenital, with absent pituitary luteinizinghormone		HP:0003623	PMID:2906226	PCS		3/3			C	HPO:probinson[2022-07-03]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0000670	PMID:7550320	PCS		1/1			P	HPO:probinson[2022-05-11];HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0008391	PMID:7550320	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0003577	PMID:9012408	PCS		2/2			C	HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0004552	PMID:9012408;PMID:7550320	PCS		3/3			P	HPO:probinson[2022-05-11];HPO:probinson[2022-05-11];HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0003341	PMID:7550320	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0008066	PMID:9012408;PMID:7550320	PCS		3/3			P	HPO:probinson[2022-05-11];HPO:probinson[2022-05-11];HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0000007	PMID:7550320	PCS					I	HPO:probinson[2022-05-11];HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0009722	PMID:7550320	PCS		1/1			P	HPO:probinson[2022-05-11];HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0007412	PMID:7550320	PCS		1/1			P	HPO:probinson[2022-05-11];HPO:probinson[2022-05-11]
OMIM:619787	Epidermolysis bullosa, junctional 4, intermediate		HP:0008404	PMID:9012408	PCS		2/2			P	HPO:probinson[2022-05-11]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0003676	PMID:34564892	PCS					C	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0003552	PMID:34825409	PCS		2/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0000750	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0031936	PMID:34564892	PCS		8/8			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0001321	PMID:34564892	PCS		1/7			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002365	PMID:34564892	PCS		1/7			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0003487	PMID:34825409	PCS		2/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002395	PMID:34825409	PCS		2/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0003593	PMID:34825409;PMID:34564892	PCS		10/10			C	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002061	PMID:34564892	PCS	HP:0011463	5/5			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002061	PMID:34825409	PCS		2/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0001270	PMID:34564892	PCS	HP:0003593	8/8			P	HPO:probinson[2023-02-06];HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0010871	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0033725	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0011448	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0007340	PMID:34825409	PCS		2/2			P	HPO:probinson[2023-02-06];HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0007002	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002936	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002317	PMID:34825409	PCS		2/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002119	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0007018	PMID:34825409	PCS		1/2			P	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0000006	PMID:34564892	PCS					I	HPO:probinson[2023-02-06]
OMIM:620106	Spastic paraplegia 88, autosomal dominant		HP:0002335	PMID:34564892	PCS		1/7			P	HPO:probinson[2023-02-06]
OMIM:618499	Noonan syndrome 11		HP:0007517	PMID:28289718	PCS		1/2			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0004322	PMID:31173466;PMID:28289718	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0001252	PMID:28289718	PCS		1/2			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0004482	PMID:31173466	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0012471	PMID:31173466	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000316	PMID:31173466	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000414	PMID:31173466	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0008872	PMID:31173466	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0001642	PMID:28289718	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000358	PMID:28289718	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000494	PMID:31173466	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0008619	PMID:31173466	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000750	PMID:31173466	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0031936	PMID:31173466	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000276	PMID:28289718	PCS		1/2			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0001263	PMID:31173466;PMID:28289718	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0005280	PMID:31173466	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0001639	PMID:31173466;PMID:28289718	PCS		2/3			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000508	PMID:28289718	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000767	PMID:28289718	PCS		1/2			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000348	PMID:28289718	PCS		1/2			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000307	PMID:28289718	PCS		1/2			P	HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0001631	PMID:28289718	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000006	PMID:31173466	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22]
OMIM:618499	Noonan syndrome 11		HP:0000369	PMID:31173466;PMID:28289718	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-22];HPO:probinson[2021-05-22]
OMIM:203500	Alkaptonuria		HP:0033704	PMID:12501223	PCS		58/58			P	HPO:probinson[2021-04-16];HPO:probinson[2021-04-16]
OMIM:203500	Alkaptonuria		HP:0003593	PMID:12501223	PCS		12/58			C	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0004382	OMIM:203500	IEA					P	HPO:iea[2009-02-17]
OMIM:203500	Alkaptonuria		HP:0033666	PMID:12501223	PCS					P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0004380	OMIM:203500	IEA					P	HPO:iea[2009-02-17]
OMIM:203500	Alkaptonuria		HP:0010501	PMID:12501223	PCS		7/58			P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0001507	OMIM:203500	IEA					P	HPO:iea[2009-02-17]
OMIM:203500	Alkaptonuria		HP:0040319	PMID:37395296	PCS		13/13			P	HPO:probinson[2024-01-06]
OMIM:203500	Alkaptonuria		HP:0001369	OMIM:203500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:203500	Alkaptonuria		HP:0008419	OMIM:203500	IEA					P	HPO:iea[2009-02-17]
OMIM:203500	Alkaptonuria		HP:0030764	PMID:12501223	PCS		58/58			P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:6000025	PMID:37395296	PCS		6/13			P	HPO:probinson[2024-01-06]
OMIM:203500	Alkaptonuria		HP:0003581	PMID:12501223	PCS		46/58			C	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:6000365	PMID:15249376	PCS					P	HPO:probinson[2024-02-27]
OMIM:203500	Alkaptonuria		HP:0003040	OMIM:203500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:203500	Alkaptonuria		HP:0004690	PMID:12501223	PCS		12/58			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0012213	PMID:12501223	PCS		1/58			P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0002829	PMID:37395296	PCS		6/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-01-06]
OMIM:203500	Alkaptonuria		HP:0001717	OMIM:203500	IEA					P	HPO:iea[2009-02-17]
OMIM:203500	Alkaptonuria		HP:0002808	PMID:12501223	PCS		31/58			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0002948	OMIM:203500	IEA					P	HPO:iea[2009-02-17]
OMIM:203500	Alkaptonuria		HP:0003419	PMID:12501223	PCS	HP:0003581	33/35			P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0000007	PMID:12501223	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0008800	PMID:12501223	PCS		33/58			P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0006467	PMID:12501223	PCS		2/58			P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0007832	OMIM:203500	IEA					P	HPO:iea[2009-02-17]
OMIM:203500	Alkaptonuria		HP:0000787	PMID:12501223	PCS		16/58			P	HPO:probinson[2021-03-12]
OMIM:203500	Alkaptonuria		HP:0004942	PMID:12501223	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-03-12]
OMIM:619977	Macular dystrophy, retinal, 4		HP:0003596	PMID:35331648	PCS		1/6			C	HPO:probinson[2022-08-17]
OMIM:619977	Macular dystrophy, retinal, 4		HP:0000662	PMID:35331648	PCS		6/6			P	HPO:probinson[2022-08-17]
OMIM:619977	Macular dystrophy, retinal, 4		HP:0011506	PMID:35331648	PCS		2/6			P	HPO:probinson[2022-08-17]
OMIM:619977	Macular dystrophy, retinal, 4		HP:0003584	PMID:35331648	PCS		5/6			C	HPO:probinson[2022-08-17]
OMIM:619977	Macular dystrophy, retinal, 4		HP:0007663	PMID:35331648	PCS		4/6			P	HPO:probinson[2022-08-17]
OMIM:619977	Macular dystrophy, retinal, 4		HP:0030619	PMID:35331648	PCS		5/6			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:619977	Macular dystrophy, retinal, 4		HP:0000006	PMID:35331648	PCS					I	HPO:probinson[2022-08-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000286	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0003016	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000343	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000463	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0010109	OMIM:239850	TAS					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0004540	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000280	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0010068	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000939	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0010055	OMIM:239850	TAS					P	HPO:probinson[2012-03-02]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0011220	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0001647	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0007665	OMIM:239850	TAS					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000774	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0001643	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000179	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000212	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000256	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0001004	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000215	OMIM:239850	TAS					P	HPO:probinson[2012-03-02]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0004634	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0004975	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0005129	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0001520	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0005445	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000431	OMIM:239850	TAS					P	HPO:probinson[2012-03-02]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0001640	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0002673	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0002750	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0003300	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0002690	OMIM:239850	TAS					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000470	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0005280	OMIM:239850	TAS					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000926	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0001537	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000527	OMIM:239850	TAS					P	HPO:probinson[2012-03-02]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0001698	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0008822	OMIM:239850	IEA					P	HPO:probinson[2009-02-17]
OMIM:239850	Hypertrichotic osteochondrodysplasia		HP:0000006	OMIM:239850	IEA					I	HPO:probinson[2009-02-17]
OMIM:207000	Anosmia for isobutyric acid		HP:0000007	OMIM:207000	IEA					I	HPO:iea[2009-02-17]
OMIM:207000	Anosmia for isobutyric acid		HP:0010633	OMIM:207000	TAS					P	HPO:probinson[2012-07-20]
OMIM:613282	Fatty liver disease, nonalcoholic, susceptibility to, 1		HP:0001397	OMIM:613282	TAS					P	HPO:skoehler[2013-06-11]
OMIM:613282	Fatty liver disease, nonalcoholic, susceptibility to, 1		HP:0001426	OMIM:613282	TAS					I	HPO:probinson[2022-09-01]
OMIM:139630	Hairy nose tip		HP:0001595	OMIM:139630	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002663	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0000121	PMID:8559248	PCS		9/28			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-11]
OMIM:300009	Dent disease 1		HP:0002982	OMIM:300009	TAS					P	HPO:probinson[2012-05-01]
OMIM:300009	Dent disease 1		HP:0003774	PMID:8559248	PCS		2/28			P	HPO:probinson[2021-07-11]
OMIM:300009	Dent disease 1		HP:0003013	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002980	OMIM:300009	TAS					P	HPO:probinson[2012-05-01]
OMIM:300009	Dent disease 1		HP:0003355	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0004322	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0000083	OMIM:300009	TAS	HP:0003581				P	HPO:probinson[2009-02-17]
OMIM:300009	Dent disease 1		HP:0003076	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0012622	OMIM:300009	TAS					P	HPO:probinson[2014-01-18]
OMIM:300009	Dent disease 1		HP:0010502	OMIM:300009	TAS					P	HPO:probinson[2012-05-01]
OMIM:300009	Dent disease 1		HP:0002979	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0000117	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0003109	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002757	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0000114	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002753	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0003029	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002653	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0003126	PMID:8559248	PCS		10/28			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-11]
OMIM:300009	Dent disease 1		HP:0002752	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0003025	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0003020	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002150	PMID:8559248	PCS		20/28			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-11]
OMIM:300009	Dent disease 1		HP:0031415	OMIM:300009	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300009	Dent disease 1		HP:0002907	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0001419	PMID:8559248	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-11]
OMIM:300009	Dent disease 1		HP:0002748	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002749	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0002148	OMIM:300009	IEA					P	HPO:iea[2009-02-17]
OMIM:300009	Dent disease 1		HP:0000787	PMID:8559248	PCS		9/28			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-11]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0002155	PMID:17332414	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0003141	PMID:17332414	PCS					P	HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0003581	PMID:17332414	PCS					C	HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0040270	OMIM:610947	IEA					P	HPO:skoehler[2019-04-18]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0005181	PMID:17332414	PCS					P	HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0000939	PMID:17332414	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0000822	PMID:17332414	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0001658	OMIM:610947	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0005978	PMID:17332414	PCS		11/15			P	HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0000006	PMID:17332414	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-30]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0001997	OMIM:610947	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0001645	OMIM:610947	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610947	Coronary artery disease, autosomal dominant 2		HP:0001952	OMIM:610947	TAS					P	HPO:skoehler[2013-11-18]
OMIM:179200	Radial heads, posterior dislocation of		HP:0005798	OMIM:179200	TAS	HP:0003577				P	HPO:probinson[2013-04-13]
OMIM:179200	Radial heads, posterior dislocation of		HP:0001377	OMIM:179200	IEA					P	HPO:iea[2009-02-17]
OMIM:179200	Radial heads, posterior dislocation of		HP:0009760	OMIM:179200	TAS					P	HPO:probinson[2013-04-13]
OMIM:179200	Radial heads, posterior dislocation of		HP:0000007	OMIM:179200	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:179200	Radial heads, posterior dislocation of		HP:0000006	OMIM:179200	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:247430	Lymphoblastic transformation, inhibition of		HP:0001939	OMIM:247430	IEA					P	HPO:iea[2009-02-17]
OMIM:247430	Lymphoblastic transformation, inhibition of		HP:0002728	OMIM:247430	IEA					P	HPO:iea[2009-02-17]
OMIM:247430	Lymphoblastic transformation, inhibition of		HP:0000007	OMIM:247430	IEA					I	HPO:iea[2009-02-17]
OMIM:134300	Facial spasm		HP:0001265	OMIM:134300	IEA					P	HPO:iea[2009-02-17]
OMIM:134300	Facial spasm		HP:0009916	OMIM:134300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:134300	Facial spasm		HP:0000006	OMIM:134300	IEA					I	HPO:iea[2009-02-17]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0003236	PMID:23453667	PCS		6/6			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0003577	PMID:23453667	PCS		4/7			C	HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000541	PMID:23453667	PCS		1/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0001321	PMID:23453667	PCS		1/7			P	HPO:skoehler[2014-04-22];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0002365	PMID:23453667	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0002352	PMID:23453667	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0001263	PMID:23453667	PCS		7/7		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0006829	PMID:23453667	PCS		4/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0002350	PMID:23453667	PCS		2/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0003560	PMID:23453667	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0003593	PMID:23453667	PCS		1/7			C	HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0012110	PMID:23453667	PCS		2/7			P	HPO:skoehler[2014-04-22];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000609	PMID:23453667	PCS		2/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0007260	PMID:23453667	PCS		4/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000518	PMID:23453667	PCS		1/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0011463	PMID:23453667	PCS		2/7			C	HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0007033	PMID:23453667	PCS		2/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000618	PMID:23453667	PCS		1/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000007	PMID:23453667	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000238	PMID:23453667	PCS		4/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000568	PMID:23453667	PCS		2/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0000545	PMID:23453667	PCS		1/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0002126	PMID:23453667	PCS		2/7			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-12]
OMIM:615181	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11)		HP:0001249	PMID:23453667	PCS		7/7			P	HPO:probinson[2022-06-12]
OMIM:130600	Elliptocytosis 2		HP:0004445	PMID:3597773	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-18]
OMIM:130600	Elliptocytosis 2		HP:0003265	PMID:27667160	PCS	HP:0003623				P	HPO:probinson[2019-07-18]
OMIM:130600	Elliptocytosis 2		HP:0001878	PMID:27667160	PCS					P	HPO:probinson[2019-07-18];HPO:probinson[2019-07-18]
OMIM:130600	Elliptocytosis 2		HP:0001923	PMID:29729090	PCS					P	HPO:probinson[2019-07-18]
OMIM:130600	Elliptocytosis 2		HP:0000006	PMID:3597773	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2019-07-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0001265	PMID:26005867	PCS		5/17			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0033748	PMID:26005867	PCS		6/14			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0012804	PMID:26005867	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0002495	PMID:26005867	PCS		1/14			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0010829	PMID:26005867	PCS		21/21			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0003593	PMID:26005867	PCS		17/18			C	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0001581	PMID:26005867	PCS		16/20			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0010831	PMID:26005867	PCS		1/14			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0011463	PMID:26005867	PCS		1/18			C	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0007021	PMID:26005867	PCS		21/21			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0000407	PMID:26005867	PCS		0/20			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0000007	PMID:26005867	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0004409	PMID:26005867	PCS		0/18			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0000559	PMID:26005867	PCS		15/20			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0000966	PMID:26005867	PCS		9/20			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0002579	PMID:26005867	PCS		0/18			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0000633	PMID:26005867	PCS		9/19			P	HPO:probinson[2022-05-18]
OMIM:616488	Neuropathy, hereditary sensory and autonomic, type VIII		HP:0001249	PMID:26005867	PCS		1/20			P	HPO:probinson[2022-05-18]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0005479	OMIM:606843	TAS				HP:0012828	P	HPO:probinson[2012-05-06]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0003496	OMIM:606843	IEA					P	HPO:iea[2009-02-17]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0002849	OMIM:606843	IEA					P	HPO:iea[2009-02-17]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0002959	OMIM:606843	TAS					P	HPO:probinson[2012-05-06]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0002718	OMIM:606843	TAS					P	HPO:probinson[2012-05-06]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0002847	OMIM:606843	IEA					P	HPO:iea[2009-02-17]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0000007	OMIM:606843	IEA					I	HPO:iea[2009-02-17]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0002720	OMIM:606843	TAS				HP:0012828	P	HPO:probinson[2012-05-06]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0001875	OMIM:606843	IEA					P	HPO:iea[2009-02-17]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0002721	OMIM:606843	TAS					P	HPO:probinson[2009-02-17]
OMIM:606843	Immunodeficiency with hyper-igm, type 3		HP:0004315	OMIM:606843	TAS				HP:0012828	P	HPO:probinson[2012-05-06]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000483	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0002188	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000486	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001250	PMID:28191889;PMID:28394464;PMID:23033978	PCS		2/7			P	HPO:probinson[2022-06-03];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001252	PMID:27824329;PMID:23033978	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0003593	PMID:28394464	PCS		1/1			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0011856	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0010722	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0008770	PMID:27824329	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000319	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0002938	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000316	PMID:28191889;PMID:28394464	PCS		2/6			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000752	PMID:28191889;PMID:27824329	PCS		2/6			P	HPO:probinson[2022-06-03];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001249	PMID:28191889;PMID:27824329;PMID:23033978	PCS		7/7			P	HPO:probinson[2022-06-03];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03];HPO:probinson[2022-06-03];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000252	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001344	PMID:23033978	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0011968	PMID:27824329;PMID:28394464	PCS		1/2			P	HPO:probinson[2022-06-03];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000490	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001263	PMID:28394464;PMID:23033978	PCS		2/2			P	HPO:probinson[2022-06-03];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001262	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000294	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000407	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000729	PMID:28191889;PMID:27824329	PCS		4/6			P	HPO:probinson[2022-06-03];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000448	PMID:23033978	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000768	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000444	PMID:23033978	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0008689	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000322	PMID:28394464;PMID:23033978	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000006	PMID:28191889	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0004602	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000369	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0003577	PMID:23033978	IEA		1/1			C	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000463	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000540	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0003691	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0002360	PMID:28191889;PMID:27824329	PCS		2/6			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0008071	PMID:23033978	PCS		1/1			H	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000737	PMID:28191889	PCS		2/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000739	PMID:27824329	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0012450	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000733	PMID:27824329	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0002714	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000218	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0006610	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000256	PMID:27824329	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001623	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0008936	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000750	PMID:27824329;PMID:23033978	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000194	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0005280	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0001518	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000426	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000821	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0025502	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000268	PMID:28191889	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0004626	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000664	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000028	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-03]
OMIM:617796	Intellectual developmental disorder, autosomal dominant 52		HP:0000666	PMID:28394464	PCS		1/1			P	HPO:probinson[2022-06-03]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0001331	OMIM:307000	TAS					P	HPO:probinson[2009-02-17]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0002410	PMID:1870106	PCS	HP:0003577	2/5	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-07]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0001419	PMID:1303258	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0001274	OMIM:307000	TAS					P	HPO:probinson[2009-02-17]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0000238	PMID:1303258;PMID:1870106	PCS		7/7	MALE		P	HPO:probinson[2022-03-07];HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0001181	PMID:1870106	PCS		1/5	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-07]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0009600	OMIM:307000	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0007016	OMIM:307000	IEA					P	HPO:iea[2009-02-17]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0001258	PMID:1870106	PCS		2/5	MALE		P	HPO:probinson[2012-07-20];HPO:probinson[2022-03-07]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0000256	OMIM:307000	IEA					P	HPO:iea[2009-02-17]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0001257	PMID:1870106	PCS		2/5	MALE		P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-07]
OMIM:307000	Hydrocephalus due to congenital stenosis of aqueduct of sylvius		HP:0001249	PMID:1870106	PCS		5/5	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-07]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0000076	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001385	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001762	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001344	OMIM:617219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0011968	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0002021	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001250	OMIM:617219	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0000072	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001263	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001290	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001182	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0003829	OMIM:617219	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0002617	OMIM:617219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0008897	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0004209	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0000787	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0000006	OMIM:617219	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617219	Chromosome 19q13.11 deletion syndrome, proximal		HP:0001249	OMIM:617219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:535000	Leber optic atrophy		HP:0000572	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0001112	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0001332	OMIM:535000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:535000	Leber optic atrophy		HP:0003198	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0001271	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0001251	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0002174	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0011675	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0003829	OMIM:535000	TAS					I	HPO:skoehler[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0001427	OMIM:535000	TAS					I	HPO:skoehler[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0000648	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0000576	OMIM:535000	IEA					P	HPO:iea[2009-02-17]
OMIM:535000	Leber optic atrophy		HP:0001138	OMIM:535000	IEA		HP:0040282			P	HPO:skoehler[2010-06-20]
OMIM:535000	Leber optic atrophy		HP:0007768	OMIM:535000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000483	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001770	PMID:31089205	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000582	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0004322	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001252	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001270	PMID:31089205	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0100704	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000319	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0002938	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0008454	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001847	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0007787	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0003701	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000677	PMID:31089205	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0002313	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000252	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000010	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001762	PMID:31089205	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0002079	PMID:31089205	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001382	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001260	PMID:31089205	PCS		1/3		HP:0012825	P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0012378	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0033044	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000646	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001537	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000007	PMID:31089205	PCS					I	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000821	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000824	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0003418	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0005617	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000823	PMID:31089205	PCS		2/3			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001510	PMID:31089205	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0001730	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619234	Short stature, oligodontia, dysmorphic facies, and motor delay		HP:0000520	PMID:31089205	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:229100	Formiminotransferase deficiency		HP:0003355	OMIM:229100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:229100	Formiminotransferase deficiency		HP:0001889	OMIM:229100	IEA					P	HPO:iea[2009-02-17]
OMIM:229100	Formiminotransferase deficiency		HP:0034742	OMIM:229100	TAS					P	HPO:probinson[2023-06-05]
OMIM:229100	Formiminotransferase deficiency		HP:0000007	OMIM:229100	IEA					I	HPO:iea[2009-02-17]
OMIM:229100	Formiminotransferase deficiency		HP:0001510	OMIM:229100	IEA					P	HPO:iea[2009-02-17]
OMIM:229100	Formiminotransferase deficiency		HP:0001249	OMIM:229100	IEA					P	HPO:iea[2009-02-17]
OMIM:229100	Formiminotransferase deficiency		HP:0003612	OMIM:229100	IEA					P	HPO:iea[2009-02-17]
OMIM:229100	Formiminotransferase deficiency		HP:0004821	OMIM:229100	IEA					P	HPO:iea[2009-02-17]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0000132	PMID:23364359	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0001022	OMIM:614076	IEA					P	HPO:probinson[2013-08-10]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0003540	PMID:12923531;PMID:23364359	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0003010	PMID:12923531	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0011891	PMID:23364359	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0000639	PMID:23364359	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0011463	PMID:23364359	PCS		1/1			C	HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0006298	PMID:23364359	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0000007	PMID:12923531	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0001107	PMID:12923531	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0007663	PMID:23364359	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0000978	PMID:12923531	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0000505	OMIM:614076	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0001934	PMID:23364359	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:614076	Hermansky-Pudlak syndrome 7		HP:0000421	PMID:23364359	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-05]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0003687	PMID:23092955	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0003577	PMID:23092955	PCS		3/3			C	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0003236	OMIM:615368	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001561	PMID:23092955	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0000573	PMID:23092955	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001371	PMID:23092955	PCS	HP:0003577	3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001252	PMID:23092955	PCS	HP:0003577	3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001284	PMID:23092955	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001290	OMIM:615368	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0010851	PMID:23092955	PCS		1/3			P	HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0002093	PMID:23092955	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001518	PMID:23092955	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0002803	PMID:23092955	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0000007	PMID:23092955	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001558	PMID:23092955	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0100309	PMID:23092955	PCS		1/3			P	HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0001522	PMID:23092955	PCS		3/3			C	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0000762	PMID:23092955	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-30]
OMIM:615368	Lethal congenital contracture syndrome 5		HP:0000883	PMID:23092955	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-30]
OMIM:260500	Papilloma of choroid plexus		HP:0025709	PMID:12085209	PCS		1/1			C	HPO:probinson[2022-12-13]
OMIM:260500	Papilloma of choroid plexus		HP:0002013	OMIM:260500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:260500	Papilloma of choroid plexus		HP:0001085	OMIM:260500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:260500	Papilloma of choroid plexus		HP:0001250	OMIM:260500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:260500	Papilloma of choroid plexus		HP:0000238	OMIM:260500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:260500	Papilloma of choroid plexus		HP:0002669	PMID:12085209	PCS	HP:0025709	1/1			P	HPO:probinson[2022-12-13]
OMIM:260500	Papilloma of choroid plexus		HP:0200022	PMID:12085209	PCS	HP:0025710	1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-13]
OMIM:260500	Papilloma of choroid plexus		HP:0002018	OMIM:260500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:260500	Papilloma of choroid plexus		HP:0002315	OMIM:260500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:260500	Papilloma of choroid plexus		HP:0000006	PMID:12085209	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2022-12-13]
OMIM:609741	Cataract 22, multiple types		HP:0100018	OMIM:609741	TAS	HP:0003577	6/6			P	HPO:probinson[2013-03-30];HPO:probinson[2023-03-13]
OMIM:609741	Cataract 22, multiple types		HP:0003577	PMID:15914629	PCS		6/6			C	HPO:probinson[2023-03-13]
OMIM:609741	Cataract 22, multiple types		HP:0000519	OMIM:609741	TAS					P	HPO:skoehler[2015-12-30]
OMIM:609741	Cataract 22, multiple types		HP:0000007	PMID:15914629	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-03-13]
OMIM:609741	Cataract 22, multiple types		HP:0000501	OMIM:609741	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:609741	Cataract 22, multiple types		HP:0000006	OMIM:609741	TAS					I	HPO:skoehler[2015-12-30]
OMIM:618880	Glaucoma, primary closed-angle		HP:0001123	PMID:30007336	PCS					P	HPO:probinson[2020-07-23]
OMIM:618880	Glaucoma, primary closed-angle		HP:0007906	PMID:30007336	PCS		5/10			P	HPO:probinson[2020-07-23]
OMIM:618880	Glaucoma, primary closed-angle		HP:0011483	PMID:30007336	PCS					P	HPO:probinson[2020-07-23]
OMIM:618880	Glaucoma, primary closed-angle		HP:0012109	PMID:30007336	PCS		2/10			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618880	Glaucoma, primary closed-angle		HP:0012796	PMID:30007336	PCS					P	HPO:probinson[2020-07-23]
OMIM:618880	Glaucoma, primary closed-angle		HP:0000006	PMID:30007336	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:610204	Pontocerebellar hypoplasia, type 5		HP:0006955	OMIM:610204	TAS				HP:0012828	P	HPO:skoehler[2009-02-17]
OMIM:610204	Pontocerebellar hypoplasia, type 5		HP:0000252	OMIM:610204	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610204	Pontocerebellar hypoplasia, type 5		HP:0003577	OMIM:610204	TAS					C	HPO:skoehler[2015-12-30]
OMIM:610204	Pontocerebellar hypoplasia, type 5		HP:0001250	OMIM:610204	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610204	Pontocerebellar hypoplasia, type 5		HP:0000007	OMIM:610204	TAS					I	HPO:skoehler[2009-02-17]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002983	OMIM:607778	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0001156	PMID:34530144	PCS		6/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0004322	PMID:34530144	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0003099	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0003097	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0005792	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0030033	OMIM:607778	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0004482	PMID:12624140	PCS					P	HPO:iea[2012-04-24]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0010049	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0100864	PMID:34530144	PCS		6/6			P	HPO:iea[2012-04-24];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0010230	PMID:12624140	PCS					P	HPO:iea[2012-04-24]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002938	PMID:34530144	PCS		4/6			P	HPO:iea[2012-04-24];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0009882	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0008873	PMID:12624140	PCS	HP:0011463				P	HPO:skoehler[2012-10-17];HPO:probinson[2024-08-03]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002812	PMID:12624140	PCS					P	HPO:iea[2012-04-24]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0006059	PMID:12624140	PCS					P	HPO:iea[2012-04-24]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0000774	PMID:34530144	PCS		3/6			P	HPO:iea[2012-04-24];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0000773	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0001821	PMID:34530144	PCS		4/4			P	HPO:iea[2012-04-24];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0001249	PMID:12624140	PCS		0/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-13]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0006216	PMID:34530144	PCS		2/2			P	HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0006438	PMID:12624140	PCS					P	HPO:iea[2012-04-24]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0009826	PMID:34530144	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002650	PMID:34530144	PCS		1/6			P	HPO:iea[2009-10-21];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0004279	OMIM:607778	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002970	PMID:12624140	PCS					P	HPO:iea[2012-04-24]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0003300	PMID:12624140	PCS					P	HPO:iea[2012-04-24]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0003022	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:6000884	PMID:12624140	PCS		1/4			P	HPO:probinson[2024-08-03]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0010575	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0010579	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0010017	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0010241	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0005819	PMID:34530144	PCS		6/6			P	HPO:iea[2009-10-21];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002869	PMID:12624140	PCS					P	HPO:iea[2012-05-28]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0000767	PMID:34530144	PCS		1/6			P	HPO:iea[2009-10-21];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0000007	PMID:12624140	PCS					I	HPO:probinson[2012-04-24];HPO:probinson[2024-08-03]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0000887	PMID:34530144	PCS		3/6			P	HPO:iea[2012-04-24];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0000768	PMID:34530144	PCS		1/6			P	HPO:iea[2012-04-24];HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0008789	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002986	PMID:34530144	PCS		3/6			P	HPO:probinson[2023-04-09]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002866	PMID:12624140	PCS					P	HPO:iea[2012-05-28]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0005736	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0001216	PMID:12624140	PCS		5/5			P	HPO:iea[2012-04-24];HPO:probinson[2024-08-03]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0002984	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0009638	PMID:12624140	PCS					P	HPO:iea[2009-10-21]
OMIM:607778	Acrocapitofemoral dysplasia		HP:0001799	PMID:34530144	PCS		4/4			P	HPO:probinson[2023-04-09]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001199	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001792	PMID:31155282	PCS		3/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001371	PMID:31155282	PCS					P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001290	PMID:31155282	PCS					P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000280	PMID:31155282	PCS		2/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0009882	PMID:31155282	PCS					P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0005807	PMID:31155282	PCS					P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000998	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001847	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001802	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0030084	PMID:31155282	PCS					P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0002219	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000218	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000455	PMID:31155282	PCS		3/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001643	PMID:31155282	PCS	HP:0003623	2/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000212	PMID:31155282	PCS		2/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000179	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001249	PMID:31155282	PCS					P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000574	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000431	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0100380	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000193	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0001263	PMID:31155282	PCS		3/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000294	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0010432	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0032524	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0100874	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0002808	PMID:31155282	PCS		1/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000527	PMID:31155282	PCS					P	HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000664	PMID:31155282	PCS		2/3			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618658	Zimmermann-Laband syndrome 3		HP:0000006	PMID:31155282	PCS					I	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:153600	Macroglobulinemia, Waldenstrom, somatic		HP:0001909	OMIM:153600	TAS		HP:0040283			P	HPO:probinson[2013-12-15]
OMIM:153600	Macroglobulinemia, Waldenstrom, somatic		HP:0001442	PMID:26244327	PCS					I	HPO:probinson[2020-07-20]
OMIM:153600	Macroglobulinemia, Waldenstrom, somatic		HP:0001271	OMIM:153600	TAS					P	HPO:iea[2009-02-17]
OMIM:153600	Macroglobulinemia, Waldenstrom, somatic		HP:0005508	OMIM:153600	IEA					P	HPO:iea[2009-02-17]
OMIM:153600	Macroglobulinemia, Waldenstrom, somatic		HP:0003459	OMIM:153600	IEA					P	HPO:iea[2009-02-17]
OMIM:153600	Macroglobulinemia, Waldenstrom, somatic		HP:0002665	OMIM:153600	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:153600	Macroglobulinemia, Waldenstrom, somatic		HP:0003347	OMIM:153600	IEA					P	HPO:iea[2009-02-17]
OMIM:604271	Growth hormone insensitivity, partial		HP:0004322	PMID:7565946	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:604271	Growth hormone insensitivity, partial		HP:0030353	PMID:7565946	PCS					P	HPO:probinson[2022-09-06]
OMIM:604271	Growth hormone insensitivity, partial		HP:0000006	PMID:7565946	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-06]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0003774	PMID:26740551	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0002202	PMID:26740551	PCS		1/1			P	HPO:probinson[2023-04-18]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0001541	PMID:26740551	PCS		1/1			P	HPO:probinson[2023-04-18]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0005565	PMID:26740551	PCS		1/1			P	HPO:probinson[2023-04-18]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0003077	OMIM:603278	IEA					P	HPO:skoehler[2013-01-11]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0000097	PMID:26740551	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-04-18]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0003073	OMIM:603278	IEA					P	HPO:skoehler[2013-01-11]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0000093	PMID:26740551	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-04-18]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0000969	OMIM:603278	IEA					P	HPO:skoehler[2013-01-11]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0001903	PMID:26740551	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0004719	PMID:26740551	PCS		1/1			P	HPO:probinson[2023-04-18]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0003829	OMIM:603278	TAS					I	HPO:skoehler[2017-07-13]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0000822	PMID:26740551	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0000006	PMID:10700177	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:603278	Focal segmental glomerulosclerosis 1		HP:0003677	PMID:26740551	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:157300	Migraine with or without aura, susceptibility to, 1		HP:0002013	OMIM:157300	IEA					P	HPO:iea[2009-02-17]
OMIM:157300	Migraine with or without aura, susceptibility to, 1		HP:0002077	OMIM:157300	IEA					P	HPO:iea[2009-02-17]
OMIM:157300	Migraine with or without aura, susceptibility to, 1		HP:0000613	OMIM:157300	IEA					P	HPO:iea[2009-02-17]
OMIM:157300	Migraine with or without aura, susceptibility to, 1		HP:0002083	OMIM:157300	IEA					P	HPO:iea[2009-02-17]
OMIM:157300	Migraine with or without aura, susceptibility to, 1		HP:0002183	OMIM:157300	IEA					P	HPO:iea[2009-02-17]
OMIM:157300	Migraine with or without aura, susceptibility to, 1		HP:0002018	OMIM:157300	IEA					P	HPO:iea[2009-02-17]
OMIM:157300	Migraine with or without aura, susceptibility to, 1		HP:0000006	OMIM:157300	IEA					I	HPO:iea[2009-02-17]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0007737	PMID:21070897	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0002166	PMID:21070897	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000662	PMID:21070897	PCS	HP:0011463				P	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000020	PMID:21070897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0001251	PMID:21070897	PCS	HP:0011463	10/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0002460	PMID:21070897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000580	PMID:21070897	PCS					P	HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0012785	PMID:21070897	PCS		1/14			P	HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000518	PMID:21070897	PCS		2/14			P	HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0011463	OMIM:609033	TAS					C	HPO:probinson[2012-04-25]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000618	OMIM:609033	TAS	HP:0003581				P	HPO:probinson[2012-04-25]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0003448	PMID:21070897	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000510	PMID:21070897	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0007843	PMID:21070897	PCS					P	HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0001249	OMIM:609033	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0003202	OMIM:609033	TAS					P	HPO:probinson[2012-04-25]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000550	OMIM:609033	IEA					P	HPO:iea[2009-02-17]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0002136	OMIM:609033	IEA					P	HPO:iea[2009-02-17]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000010	PMID:21070897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0002650	PMID:21070897	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0031936	PMID:21070897	PCS		1/14			P	HPO:skoehler[2019-02-22];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0002571	OMIM:609033	IEA	HP:0011463				P	HPO:iea[2009-02-17]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0001284	PMID:21070897	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0030529	PMID:21070897	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0010871	PMID:21070897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0040272	PMID:21070897	PCS					P	HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0010831	PMID:21070897	PCS		12/14			P	HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0012385	PMID:21070897	PCS		1/14			P	HPO:skoehler[2013-10-22];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0011096	PMID:21070897	PCS					P	HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0009473	OMIM:609033	IEA					P	HPO:iea[2009-02-17]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000007	PMID:21070897	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0000648	OMIM:609033	IEA					P	HPO:iea[2009-02-17]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0002403	OMIM:609033	IEA					P	HPO:iea[2009-02-17]
OMIM:609033	Ataxia, posterior column, with retinitis pigmentosa		HP:0003677	PMID:21070897	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0002783	PMID:25525876	PCS		4/4			P	HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0000265	PMID:25525876	PCS		1/4			P	HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0002110	PMID:25414442;PMID:25525876	PCS		3/6			P	HPO:probinson[2021-06-30];HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0003496	PMID:25414442	PCS		1/2			P	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0001890	PMID:25414442;PMID:25525876	PCS		5/6			P	HPO:probinson[2021-06-30];HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0001263	PMID:25525876	PCS		4/4			P	HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0003593	PMID:25525876	PCS		4/4			C	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0032247	PMID:25525876	PCS		2/4			P	HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0001904	PMID:25525876	PCS		3/4			P	HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0003819	PMID:25414442	PCS		1/2			C	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0011463	PMID:25414442	PCS		2/2			C	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0011342	PMID:25414442	PCS		1/2			P	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0040167	PMID:25414442	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0000007	PMID:25525876	PCS					I	HPO:probinson[2021-05-19];HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0000403	PMID:25525876	PCS		4/4			P	HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0002716	PMID:25414442	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0006268	PMID:25414442	PCS		1/2			P	HPO:probinson[2021-06-30]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0001973	PMID:25414442;PMID:25525876	PCS		5/6			P	HPO:probinson[2021-06-30];HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0410028	PMID:25525876	PCS		1/4			P	HPO:probinson[2021-05-19]
OMIM:619220	Immunodeficiency 78 with autoimmunity and developmental delay		HP:0003237	PMID:25414442	PCS		2/2			P	HPO:probinson[2021-06-30];HPO:probinson[2021-06-30]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0000044	PMID:25248098	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0010627	PMID:25248098	PCS		1/3			P	HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001321	PMID:25248098	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001332	PMID:25248098	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0004322	PMID:25248098	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001260	PMID:25248098	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001271	PMID:25248098	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001251	PMID:25248098	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001270	PMID:25248098	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0100651	PMID:25248098	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0011787	PMID:25248098	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0031097	PMID:25248098	PCS		0/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0011463	PMID:25248098	PCS		3/3			C	HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0000007	PMID:25248098	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001943	PMID:25248098	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0004408	PMID:25248098	PCS		0/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0008897	PMID:25248098	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0008734	PMID:25248098	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0040217	PMID:25248098	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:616113	Polyendocrine-polyneuropathy syndrome		HP:0001730	PMID:25248098	PCS		1/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:615432	Specific language impairment 5		HP:0002463	PMID:31664034	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2021-02-20]
OMIM:615432	Specific language impairment 5		HP:0000750	PMID:23810381	PCS		26/26			P	HPO:probinson[2021-02-20]
OMIM:615432	Specific language impairment 5		HP:0000729	PMID:31664034	TAS		4/15			P	HPO:skoehler[2013-11-18];HPO:probinson[2021-02-20]
OMIM:615432	Specific language impairment 5		HP:0001263	PMID:31664034	PCS		4/15			P	HPO:skoehler[2013-11-18];HPO:probinson[2021-02-20]
OMIM:615432	Specific language impairment 5		HP:0003829	PMID:31664034	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2021-02-20]
OMIM:615432	Specific language impairment 5		HP:0030890	PMID:23810381	PCS		22/31			P	HPO:probinson[2021-02-20]
OMIM:615432	Specific language impairment 5		HP:0000006	PMID:23810381	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2021-02-20]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002322	PMID:28137957	PCS		1/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0003477	PMID:28137957	PCS		4/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002067	PMID:28137957	PCS		1/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002120	PMID:28137957	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001272	PMID:28137957	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002066	PMID:28137957	PCS		3/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001251	PMID:27217339;PMID:28137957	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0000639	PMID:27217339	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0000738	PMID:28137957	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0000718	PMID:28137957	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002936	PMID:28137957	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002518	PMID:28137957	PCS		2/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001268	PMID:27217339	PCS		1/1			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0020049	PMID:27217339;PMID:28137957	PCS		2/6			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001347	PMID:28137957	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002510	PMID:27217339	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001300	PMID:28137957	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0000012	PMID:28137957	PCS		2/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001761	PMID:27217339;PMID:28137957	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0003487	PMID:28137957	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002495	PMID:28137957	PCS		3/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001260	PMID:28137957	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0003581	PMID:28137957	PCS		5/5			C	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0010830	PMID:28137957	PCS		3/5			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0000605	PMID:28137957	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0000726	PMID:28137957	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0000007	PMID:28137957	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0007256	PMID:28137957	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0002527	PMID:27217339	PCS		1/1			P	HPO:probinson[2021-02-13]
OMIM:617225	Spastic paraplegia 78, autosomal recessive		HP:0001258	PMID:27217339	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:618116	Bone marrow failure syndrome 4		HP:0004313	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0003577	OMIM:618116	IEA					C	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0000252	OMIM:618116	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618116	Bone marrow failure syndrome 4		HP:0008905	OMIM:618116	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618116	Bone marrow failure syndrome 4		HP:0001882	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0004322	OMIM:618116	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618116	Bone marrow failure syndrome 4		HP:0001263	OMIM:618116	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618116	Bone marrow failure syndrome 4		HP:0011800	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0000958	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0001903	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0001999	OMIM:618116	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0000964	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0000007	OMIM:618116	IEA					I	HPO:skoehler[2019-04-18]
OMIM:618116	Bone marrow failure syndrome 4		HP:0005528	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0002205	OMIM:618116	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618116	Bone marrow failure syndrome 4		HP:0001873	OMIM:618116	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618116	Bone marrow failure syndrome 4		HP:0000369	OMIM:618116	IEA					P	HPO:skoehler[2019-02-15]
OMIM:619208	Olmsted syndrome 2		HP:0002289	PMID:31361044	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0002224	PMID:30321533	PCS		2/4			P	HPO:probinson[2021-03-28];HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0001036	PMID:31361044	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0033707	PMID:30321533;PMID:31361044	PCS		5/5			P	HPO:probinson[2021-04-16]
OMIM:619208	Olmsted syndrome 2		HP:0003593	PMID:30321533	PCS		4/4			C	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0030044	PMID:31361044	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0025092	PMID:30321533;PMID:31361044	PCS		2/2			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0008070	PMID:31361044	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0100825	PMID:30321533	PCS		4/4			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0000989	PMID:31361044	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0000972	PMID:31361044	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0000982	PMID:30321533	PCS		4/4			P	HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0000006	PMID:30321533	PCS					I	HPO:probinson[2021-03-28];HPO:probinson[2021-03-28]
OMIM:619208	Olmsted syndrome 2		HP:0000962	PMID:30321533	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000286	PMID:16380919	PCS		12/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0004322	OMIM:601321	IEA		10/22			P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0002162	PMID:16380919	PCS		17/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0005272	OMIM:601321	IEA					P	HPO:iea[2009-02-17]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000917	OMIM:601321	TAS					P	HPO:skoehler[2013-05-03]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0012471	PMID:16380919	PCS		9/22			P	HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000915	OMIM:601321	IEA					P	HPO:skoehler[2019-02-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000316	PMID:16380919	PCS		20/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0001328	OMIM:601321;PMID:16380919	PCS		21/30			P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000997	PMID:16380919	PCS		16/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0007565	PMID:16380919	PCS		22/22			P	HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0001324	OMIM:601321	IEA					P	HPO:iea[2009-02-17]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000256	PMID:16380919	PCS		14/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0001642	PMID:16380919	PCS		4/22			P	HPO:skoehler[2010-06-20];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000358	PMID:16380919	PCS		22/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0001249	PMID:16380919	PCS		4/22			P	HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0003006	PMID:16380919	PCS		1/21			P	HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0001067	PMID:16380919	PCS		9/22			P	HPO:skoehler[2010-06-20];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000494	PMID:16380919	PCS		18/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000750	OMIM:601321	TAS					P	HPO:skoehler[2013-05-03]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0002650	PMID:16380919	PCS		9/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0001684	OMIM:601321	IEA					P	HPO:iea[2009-02-17]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0001263	OMIM:601321	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000272	PMID:16380919	PCS		5/22			P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000470	OMIM:601321	TAS					P	HPO:skoehler[2013-05-03]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0011800	OMIM:601321	TAS					P	HPO:skoehler[2013-11-28]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0005280	OMIM:601321	TAS					P	HPO:skoehler[2015-10-05]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000508	PMID:16380919	PCS		15/22			P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000767	PMID:16542390	PCS		4/8			P	HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0030052	PMID:16380919	PCS					P	HPO:skoehler[2014-09-21];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0002967	PMID:16380919	PCS		7/22			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0009732	PMID:16380919	PCS		1/22			P	HP:probinson[2019-01-22];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0009734	PMID:16380919	PCS		4/14			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000465	PMID:16380919	PCS		14/22			P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000006	PMID:16380919	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000028	PMID:16380919	PCS		1/12	MALE		P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0009737	PMID:16380919	PCS		12/20			P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:601321	Neurofibromatosis-Noonan syndrome		HP:0000369	PMID:16380919	PCS		22/22			P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0003577	PMID:10932188	PCS					C	HPO:probinson[2022-08-27]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000288	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0002164	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0010709	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0010621	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0410030	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0045075	OMIM:225060	TAS					P	HPO:probinson[2022-05-07]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0011359	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000975	PMID:25913853	PCS		0/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000972	PMID:25913853	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000411	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000653	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000674	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000175	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0001047	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0002299	OMIM:225060	IEA					P	HPO:skoehler[2018-10-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0002296	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000691	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000272	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0010554	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000968	PMID:25913853	PCS		1/1			P	HPO:iea[2015-01-14]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000668	PMID:25913853	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000007	PMID:10932188	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000204	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000369	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000347	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000325	OMIM:225060	IEA					P	HPO:iea[2009-02-17]
OMIM:225060	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0003777	PMID:25913853	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:618670	Spermatogenic failure 41		HP:0003251	PMID:31621862	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618670	Spermatogenic failure 41		HP:0032562	PMID:31621862	PCS		1/1			P	HPO:probinson[2020-07-11]
OMIM:618670	Spermatogenic failure 41		HP:0000007	PMID:31621862	PCS					I	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618670	Spermatogenic failure 41		HP:0012208	PMID:31621862	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618670	Spermatogenic failure 41		HP:0000798	PMID:31621862	PCS		1/1			P	HPO:probinson[2020-07-11]
OMIM:618670	Spermatogenic failure 41		HP:0032559	PMID:31621862	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:228550	Myofibromatosis, infantile, 1		HP:0003593	PMID:23731537	PCS					C	HPO:probinson[2022-10-23]
OMIM:228550	Myofibromatosis, infantile, 1		HP:0020135	PMID:23731537	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-23]
OMIM:228550	Myofibromatosis, infantile, 1		HP:0010614	PMID:23731537	PCS					P	HPO:skoehler[2013-10-07];HPO:probinson[2022-10-23]
OMIM:228550	Myofibromatosis, infantile, 1		HP:0000006	PMID:23731537	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-23]
OMIM:613731	Retinitis pigmentosa 4		HP:0007737	PMID:33777460	PCS		2/2			P	HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0000662	PMID:33777460	PCS	HP:0011463	2/2			P	HPO:probinson[2012-04-04];HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0001123	PMID:33777460	PCS		2/2			P	HPO:probinson[2012-04-04];HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0000580	OMIM:613731	IEA					P	HPO:probinson[2012-04-04]
OMIM:613731	Retinitis pigmentosa 4		HP:0000518	PMID:33777460	PCS		0/2			P	HPO:probinson[2012-04-04];HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0011463	PMID:33777460	PCS		2/2			C	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0000618	OMIM:613731	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613731	Retinitis pigmentosa 4		HP:0000007	OMIM:613731	IEA					I	HPO:probinson[2012-04-04]
OMIM:613731	Retinitis pigmentosa 4		HP:0007663	PMID:33777460	PCS	HP:0003581	2/2			P	HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0000510	PMID:33777460	PCS		2/2			P	HPO:probinson[2012-04-04];HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0007843	PMID:33777460	PCS		2/2			P	HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0000006	PMID:2137202	PCS					I	HPO:probinson[2012-04-04];HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0000512	PMID:33777460	PCS		2/2			P	HPO:probinson[2012-04-04];HPO:probinson[2022-11-07]
OMIM:613731	Retinitis pigmentosa 4		HP:0001105	PMID:33777460	PCS		2/2			P	HPO:probinson[2022-11-07]
OMIM:616649	Spherocytosis, type 2		HP:0005502	PMID:11703334	PCS		1/1			P	HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0004444	PMID:6215583;PMID:19538529	PCS		5/5			P	HPO:probinson[2019-11-28];HPO:probinson[2019-11-28];HPO:skoehler[2015-11-29];HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0002904	PMID:11703334	PCS		2/2			P	HPO:skoehler[2015-11-29];HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0001927	PMID:6215583	PCS		3/3			P	HPO:probinson[2019-11-28];HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0001878	PMID:11703334	PCS		2/2			P	HPO:skoehler[2015-11-29];HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0001923	PMID:11703334;PMID:19538529	PCS		12/12			P	HPO:probinson[2019-11-28];HPO:probinson[2019-11-28];HPO:skoehler[2015-11-29];HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0000952	PMID:11703334	TAS		2/2			P	HPO:skoehler[2015-11-29];HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0001744	PMID:11703334	TAS		2/2			P	HPO:skoehler[2015-11-29];HPO:probinson[2019-11-28]
OMIM:616649	Spherocytosis, type 2		HP:0000006	PMID:19538529	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-11-28]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0000175	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0001597	PMID:15106123	PCS		0/15			P	HPO:probinson[2018-03-07];HPO:probinson[2024-03-08]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0004322	OMIM:147891	TAS					P	HPO:probinson[2016-07-20]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0003097	OMIM:147891	TAS				HP:0012826	P	HPO:skoehler[2017-07-13]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0003065	PMID:15106123	PCS		15/15			P	HPO:probinson[2018-03-07];HPO:probinson[2024-03-08]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0005682	OMIM:147891	TAS					P	HPO:skoehler[2017-07-13]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0003370	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0008784	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0002999	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0006443	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0002812	OMIM:147891	TAS					P	HPO:probinson[2016-07-20]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0000218	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0008368	OMIM:147891	TAS					P	HPO:probinson[2016-07-20]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0001852	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0001763	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0000006	PMID:15106123	PCS					I	HPO:probinson[2018-03-07];HPO:probinson[2024-03-08]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0000347	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:147891	Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension		HP:0008801	OMIM:147891	TAS					P	HPO:probinson[2018-03-07]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001298	PMID:21057504	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001297	OMIM:611126	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0003577	PMID:21057504	PCS		4/4			C	HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001399	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001252	OMIM:611126	TAS					P	HPO:skoehler[2014-11-26]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001290	OMIM:611126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0002181	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0011923	PMID:21057504	PCS		4/4			P	HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0003819	PMID:21057504	PCS		2/4			C	HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001639	PMID:21057504	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0000007	PMID:21057504	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001635	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001943	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001324	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001522	PMID:21057504	PCS		1/4			C	HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0002910	OMIM:611126	TAS					P	HPO:probinson[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001873	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0003215	PMID:21057504	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001414	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0001644	OMIM:611126	IEA					P	HPO:iea[2009-02-17]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0003546	PMID:21057504	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-15]
OMIM:611126	Mitochondrial complex I deficiency, nuclear type 20		HP:0003128	PMID:21057504	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-15]
OMIM:265450	Pulmonary venoocclusive disease 1		HP:0006518	PMID:12446270	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-03-22]
OMIM:265450	Pulmonary venoocclusive disease 1		HP:0025180	PMID:12446270	PCS		1/1			P	HPO:probinson[2020-03-22]
OMIM:265450	Pulmonary venoocclusive disease 1		HP:0002092	PMID:16429395	PCS					P	HPO:skoehler[2013-05-29];HPO:probinson[2020-03-22]
OMIM:265450	Pulmonary venoocclusive disease 1		HP:0030848	PMID:12446270	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-03-22]
OMIM:265450	Pulmonary venoocclusive disease 1		HP:0031687	PMID:12446270	PCS		1/1			P	HPO:probinson[2020-03-22]
OMIM:265450	Pulmonary venoocclusive disease 1		HP:0030879	PMID:12446270	PCS		1/1			P	HPO:probinson[2020-03-22]
OMIM:265450	Pulmonary venoocclusive disease 1		HP:0000006	PMID:16429403	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2020-03-22]
OMIM:212800	Cephalin lipidosis		HP:0001939	OMIM:212800	IEA					P	HPO:iea[2009-02-17]
OMIM:212800	Cephalin lipidosis		HP:0000007	OMIM:212800	IEA					I	HPO:iea[2009-02-17]
OMIM:212800	Cephalin lipidosis		HP:0001249	OMIM:212800	IEA					P	HPO:iea[2009-02-17]
OMIM:212800	Cephalin lipidosis		HP:0001743	OMIM:212800	IEA					P	HPO:iea[2009-02-17]
OMIM:617557	Gabriele-De vries syndrome		HP:0000164	PMID:28575647	PCS		2/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0002188	PMID:28575647	PCS		1/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000486	PMID:28575647	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001332	PMID:28575647	PCS		2/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001252	PMID:28575647	PCS		3/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0045075	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0002539	PMID:28575647	PCS		1/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0100807	PMID:28575647	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001249	PMID:28575647	PCS		9/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000358	PMID:28575647	PCS		6/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0020206	PMID:28575647	PCS		7/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0031834	PMID:28575647	PCS		1/8			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000297	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000494	PMID:28575647	PCS		5/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0011968	PMID:28575647	PCS		9/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001263	PMID:28575647	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000729	PMID:28575647	PCS		2/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001852	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000201	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000006	PMID:28575647	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000369	PMID:28575647	PCS		1/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001337	PMID:28575647	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000324	PMID:28575647	PCS		7/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000126	PMID:28575647	PCS		2/8			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001655	PMID:28575647	PCS		1/8			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0003577	PMID:28575647	PCS		10/10			C	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001270	PMID:28575647	PCS		10/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0006094	PMID:28575647	PCS		2/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0002719	PMID:28575647	PCS		1/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000739	PMID:28575647	PCS		1/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000337	PMID:28575647	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001822	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0002999	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0002515	PMID:28575647	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000218	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000455	PMID:28575647	PCS		5/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000179	PMID:28575647	PCS		8/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0002236	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0006956	PMID:28575647	PCS		1/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000750	PMID:28575647	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0005684	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000272	PMID:28575647	PCS		8/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000074	PMID:28575647	PCS		1/8			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0011225	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000506	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000629	PMID:28575647	PCS		6/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000508	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000307	PMID:28575647	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0030051	PMID:28575647	PCS		1/9			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000268	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0001511	PMID:28575647	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0007018	PMID:28575647	PCS		1/10			P	HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000028	PMID:28575647	PCS		1/5	MALE		P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-22]
OMIM:617557	Gabriele-De vries syndrome		HP:0000347	PMID:28575647	PCS		1/7			P	HPO:probinson[2022-10-22]
OMIM:618664	Spermatogenic failure 40		HP:0032560	PMID:31413122	PCS					P	HPO:probinson[2020-06-23]
OMIM:618664	Spermatogenic failure 40		HP:0003251	PMID:31413122	PCS		3/3			P	HPO:probinson[2020-06-23]
OMIM:618664	Spermatogenic failure 40		HP:0000007	PMID:28552195	PCS					I	HPO:probinson[2020-11-26]
OMIM:618664	Spermatogenic failure 40		HP:0012208	PMID:31413122	PCS		3/3			P	HPO:probinson[2020-06-23]
OMIM:618664	Spermatogenic failure 40		HP:0000798	PMID:31413122	PCS		3/3			P	HPO:probinson[2020-06-23]
OMIM:618664	Spermatogenic failure 40		HP:0032558	PMID:31413122	PCS					P	HPO:probinson[2020-06-23]
OMIM:618664	Spermatogenic failure 40		HP:0032559	PMID:31413122	PCS					P	HPO:probinson[2020-06-23]
OMIM:600995	Nephrotic syndrome, type 2		HP:0003774	PMID:11729243	PCS		7/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-15]
OMIM:600995	Nephrotic syndrome, type 2		HP:0003621	OMIM:600995	IEA		2/9			C	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:600995	Nephrotic syndrome, type 2		HP:0000100	PMID:11729243	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:600995	Nephrotic syndrome, type 2		HP:0000969	OMIM:600995	IEA					P	HPO:iea[2009-02-17]
OMIM:600995	Nephrotic syndrome, type 2		HP:0003077	OMIM:600995	IEA					P	HPO:iea[2009-02-17]
OMIM:600995	Nephrotic syndrome, type 2		HP:0011463	PMID:11729243	PCS		7/9			C	HPO:probinson[2022-05-15]
OMIM:600995	Nephrotic syndrome, type 2		HP:0000097	PMID:11729243	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-15]
OMIM:600995	Nephrotic syndrome, type 2		HP:0003073	OMIM:600995	IEA					P	HPO:iea[2009-02-17]
OMIM:600995	Nephrotic syndrome, type 2		HP:0000007	PMID:10742096	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-15]
OMIM:600995	Nephrotic syndrome, type 2		HP:0000093	PMID:11729243	PCS		9/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-15]
OMIM:600995	Nephrotic syndrome, type 2		HP:0003678	PMID:11729243	PCS					C	HPO:skoehler[2013-05-31];HPO:probinson[2022-05-15]
OMIM:601453	Trichodental dysplasia		HP:0000252	OMIM:601453	TAS				HP:0012827	P	HPO:probinson[2009-02-17]
OMIM:601453	Trichodental dysplasia		HP:0002213	OMIM:601453	TAS					P	HPO:skoehler[2013-06-11]
OMIM:601453	Trichodental dysplasia		HP:0000694	OMIM:601453	IEA					P	HPO:iea[2009-02-17]
OMIM:601453	Trichodental dysplasia		HP:0002299	OMIM:601453	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601453	Trichodental dysplasia		HP:0000668	OMIM:601453	IEA					P	HPO:iea[2009-02-17]
OMIM:601453	Trichodental dysplasia		HP:0002217	OMIM:601453	IEA					P	HPO:iea[2009-02-17]
OMIM:601453	Trichodental dysplasia		HP:0000006	OMIM:601453	IEA					I	HPO:iea[2009-02-17]
OMIM:601453	Trichodental dysplasia		HP:0008070	OMIM:601453	IEA					P	HPO:iea[2009-02-17]
OMIM:601453	Trichodental dysplasia		HP:0000698	OMIM:601453	TAS					P	HPO:probinson[2009-02-17]
OMIM:615426	Amyotrophic lateral sclerosis 20		HP:0003155	PMID:23455423	PCS					P	HPO:probinson[2015-05-10]
OMIM:615426	Amyotrophic lateral sclerosis 20		HP:0003560	PMID:23455423	PCS	HP:0003584				P	HPO:probinson[2015-05-10]
OMIM:615426	Amyotrophic lateral sclerosis 20		HP:0007354	OMIM:615426	IEA					P	HPO:skoehler[2015-12-30]
OMIM:615426	Amyotrophic lateral sclerosis 20		HP:0003805	PMID:23455423	PCS					P	HPO:probinson[2015-05-10]
OMIM:615426	Amyotrophic lateral sclerosis 20		HP:0100299	PMID:23455423	PCS					P	HPO:probinson[2015-05-10]
OMIM:615426	Amyotrophic lateral sclerosis 20		HP:0000006	PMID:23455423	PCS					I	HPO:probinson[2015-05-10]
OMIM:605635	Hyperaldosteronism, familial, type II		HP:0003621	PMID:29403012	PCS		1/1			C	HPO:probinson[2022-11-10]
OMIM:605635	Hyperaldosteronism, familial, type II		HP:0000859	PMID:29403011	PCS					P	HPO:probinson[2022-11-10]
OMIM:605635	Hyperaldosteronism, familial, type II		HP:0003829	PMID:29403011	PCS					I	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-10]
OMIM:605635	Hyperaldosteronism, familial, type II		HP:0000822	PMID:29403012	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:605635	Hyperaldosteronism, familial, type II		HP:0002900	PMID:29403012	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-10]
OMIM:605635	Hyperaldosteronism, familial, type II		HP:0000006	PMID:29403011	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:219000	Fraser syndrome		HP:0002223	OMIM:219000	PCS					P	HPO:probinson[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000561	OMIM:219000	PCS					P	HPO:probinson[2012-03-02]
OMIM:219000	Fraser syndrome		HP:0007957	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000089	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0001250	PMID:16894541	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0008609	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0003191	OMIM:219000	TAS					P	HPO:probinson[2013-08-09]
OMIM:219000	Fraser syndrome		HP:0001607	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000316	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000678	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000238	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0001602	PMID:16894541	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0000636	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0001126	PMID:16894541	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0002536	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0001249	OMIM:219000	PCS					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000175	PMID:16894541	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0000252	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000054	OMIM:219000	PCS					P	HPO:probinson[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0004378	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000452	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0002475	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0010554	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000528	PMID:16894541	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0000007	PMID:12766769	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0000689	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0007993	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000405	PMID:16894541	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0007633	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000047	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000204	PMID:16894541	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0000369	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000445	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000324	PMID:16894541	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0001551	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0001792	PMID:16894541	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0002089	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0002244	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0005950	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000183	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0005352	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0002084	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:6000613	PMID:7747754	PCS	HP:0011461	1/1			P	HPO:probinson[2024-05-09]
OMIM:219000	Fraser syndrome		HP:0008750	OMIM:219000	TAS					P	HPO:skoehler[2014-06-24]
OMIM:219000	Fraser syndrome		HP:0000618	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000777	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0001627	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0009601	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000813	PMID:16894541	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:219000	Fraser syndrome		HP:0000378	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0006610	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0009767	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0008678	OMIM:219000	PCS					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000413	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0008559	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0006714	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0005325	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0007925	OMIM:219000	TAS					P	HPO:probinson[2012-06-10]
OMIM:219000	Fraser syndrome		HP:0000431	OMIM:219000	PCS					P	HPO:probinson[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000430	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0004112	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0001362	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0003183	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0005280	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0008665	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000028	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0002006	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:219000	Fraser syndrome		HP:0000148	OMIM:219000	IEA					P	HPO:iea[2009-02-17]
OMIM:254100	Muscular dystrophy, congenital, with rapid progression		HP:0003560	OMIM:254100	IEA					P	HPO:iea[2009-02-17]
OMIM:254100	Muscular dystrophy, congenital, with rapid progression		HP:0000007	OMIM:254100	IEA					I	HPO:iea[2009-02-17]
OMIM:254100	Muscular dystrophy, congenital, with rapid progression		HP:0001324	OMIM:254100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254100	Muscular dystrophy, congenital, with rapid progression		HP:0003678	OMIM:254100	IEA					C	HPO:iea[2009-02-17]
OMIM:620310	Congenital myopathy 20		HP:0000286	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0030674	PMID:31230720	PCS		1/2			C	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0001250	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003551	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003691	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0034675	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003391	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0030319	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0010942	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0009381	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0001508	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0009487	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0011220	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0009046	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0000337	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0000218	PMID:29498452;PMID:31230720	PCS		2/3			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003803	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003701	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0002359	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0000275	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003202	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003621	PMID:29498452	PCS		1/1			C	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003687	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0002650	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0000750	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0001762	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0031936	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0000592	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0001263	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0005280	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0002827	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0002803	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0000007	PMID:29498452	PCS					I	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0000347	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003798	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0034391	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0003557	PMID:29498452	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:620310	Congenital myopathy 20		HP:0002028	PMID:31230720	PCS		1/2			P	HPO:probinson[2023-07-11]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0003698	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0003076	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0001290	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0003074	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0001270	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0100651	PMID:16613899	IEA	HP:0003623	1/1			P	HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0012434	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0002919	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0011182	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0001518	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0000007	PMID:17668386	PCS					I	HPO:probinson[2020-11-26]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0001324	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0002305	PMID:16613899	PCS		1/1			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618857	Diabetes mellitus, permanent neonatal 3, with or without neurologic features		HP:0000006	PMID:16613899	PCS					I	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0003621	PMID:24648384	PCS		1/1			C	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0003016	OMIM:250400	TAS					P	HPO:probinson[2012-05-26]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0003498	OMIM:250400	IEA					P	HPO:iea[2009-02-17]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0004322	PMID:24648384	PCS		1/3			P	HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0006409	OMIM:250400	IEA					P	HPO:iea[2009-02-17]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0005871	OMIM:250400	TAS					P	HPO:probinson[2009-02-17]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0003593	PMID:19615667	PCS		1/1			C	HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0030839	PMID:24648384	PCS		2/3			P	HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0001270	OMIM:250400	IEA					P	HPO:iea[2009-02-17]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0100255	OMIM:250400	TAS		3/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0010886	PMID:24648384	PCS		1/3			P	HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0006385	OMIM:250400	IEA					P	HPO:iea[2009-02-17]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0002979	PMID:19615667	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0000007	PMID:19615667	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0002515	OMIM:250400	IEA					P	HPO:iea[2009-02-17]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0002857	OMIM:250400	IEA					P	HPO:iea[2009-02-17]
OMIM:250400	Metaphyseal chondrodysplasia, Spahr type		HP:0004979	OMIM:250400	TAS					P	HPO:probinson[2009-02-17]
OMIM:227850	Fanconi-Like syndrome		HP:0007606	OMIM:227850	IEA					P	HPO:iea[2009-02-17]
OMIM:227850	Fanconi-Like syndrome		HP:0002783	OMIM:227850	IEA					P	HPO:iea[2009-02-17]
OMIM:227850	Fanconi-Like syndrome		HP:0005939	OMIM:227850	IEA					P	HPO:iea[2009-02-17]
OMIM:227850	Fanconi-Like syndrome		HP:0000007	OMIM:227850	IEA					I	HPO:iea[2009-02-17]
OMIM:227850	Fanconi-Like syndrome		HP:0001876	OMIM:227850	IEA					P	HPO:iea[2009-02-17]
OMIM:227850	Fanconi-Like syndrome		HP:0002754	OMIM:227850	IEA					P	HPO:iea[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001254	OMIM:238970	TAS					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002168	PMID:11355015	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0006846	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002169	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001410	OMIM:238970	IEA					P	HPO:probinson[2012-04-04]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0200119	OMIM:238970	TAS					P	HPO:skoehler[2013-06-11]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001310	PMID:11355015	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002123	OMIM:238970	TAS					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002120	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001252	OMIM:238970	TAS					P	HPO:skoehler[2014-11-26]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002240	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0003593	PMID:11355015	PCS		1/2			C	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002064	PMID:11355015	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001270	PMID:11355015	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0012026	PMID:11355015	PCS		2/2			P	HPO:probinson[2012-07-26];HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001508	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0034464	PMID:11355015	PCS		2/2			P	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001328	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001987	PMID:11355015	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001249	OMIM:238970	TAS		HP:0040282			P	HPO:skoehler[2013-06-03]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002038	PMID:11355015	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002313	OMIM:238970	TAS					P	HPO:probinson[2012-07-21]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0000533	OMIM:238970	IEA		HP:0040284			P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001347	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002311	OMIM:238970	IEA					P	HPO:probinson[2012-07-21]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0003621	PMID:11355015	PCS		1/2			C	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001264	PMID:11355015	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001289	OMIM:238970	IEA					P	HPO:skoehler[2018-10-08]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002078	PMID:11355015	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002572	OMIM:238970	TAS					P	HPO:skoehler[2012-10-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002495	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001263	OMIM:238970	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:probinson[2012-04-04]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0002075	PMID:11355015	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0007256	PMID:11355015	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0000007	PMID:10369256	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0007894	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001258	PMID:11355015	PCS		2/2			P	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0000762	OMIM:238970	IEA					P	HPO:probinson[2009-02-17]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001257	OMIM:238970	TAS					P	HPO:probinson[2012-07-21]
OMIM:238970	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome		HP:0001259	OMIM:238970	TAS					P	HPO:probinson[2012-07-21]
OMIM:613916	Deafness, autosomal recessive 89		HP:0000407	PMID:23768514	PCS		13/13			P	HPO:probinson[2023-06-04]
OMIM:613916	Deafness, autosomal recessive 89		HP:0003593	PMID:23768514	PCS		13/13			C	HPO:probinson[2023-06-04]
OMIM:613916	Deafness, autosomal recessive 89		HP:0000007	PMID:23768514	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:613916	Deafness, autosomal recessive 89		HP:0001756	PMID:23768514	PCS		0/13			P	HPO:probinson[2023-06-04]
OMIM:163700	Nipples, supernumerary		HP:0000077	OMIM:163700	IEA					P	HPO:iea[2009-02-17]
OMIM:163700	Nipples, supernumerary		HP:0002558	OMIM:163700	IEA					P	HPO:iea[2009-02-17]
OMIM:163700	Nipples, supernumerary		HP:0000006	OMIM:163700	IEA					I	HPO:iea[2009-02-17]
OMIM:163700	Nipples, supernumerary		HP:0000765	OMIM:163700	IEA					P	HPO:iea[2009-02-17]
OMIM:619585	Spermatogenic failure 58		HP:0033393	PMID:33689014	PCS		2/2			P	HPO:probinson[2021-11-15]
OMIM:619585	Spermatogenic failure 58		HP:0034011	PMID:33689014	PCS		1/2			P	HPO:probinson[2021-11-15];HPO:probinson[2021-11-15]
OMIM:619585	Spermatogenic failure 58		HP:0003251	PMID:33689014	IEA		2/2			P	HPO:probinson[2021-11-15]
OMIM:619585	Spermatogenic failure 58		HP:0011462	PMID:33689014	PCS		2/2			C	HPO:probinson[2021-11-15]
OMIM:619585	Spermatogenic failure 58		HP:0000007	PMID:33689014	PCS					I	HPO:probinson[2021-11-15]
OMIM:619585	Spermatogenic failure 58		HP:0012208	PMID:33689014	PCS		1/2			P	HPO:probinson[2021-11-15]
OMIM:619585	Spermatogenic failure 58		HP:0000798	PMID:33689014	PCS		1/2			P	HPO:probinson[2021-11-15]
OMIM:619585	Spermatogenic failure 58		HP:0032559	PMID:33689014	PCS		2/2			P	HPO:probinson[2021-11-15]
OMIM:609796	Peeling skin syndrome 2		HP:0034838	PMID:16380904	PCS		1/1			P	HPO:probinson[2024-03-14];HPO:probinson[2024-03-14]
OMIM:609796	Peeling skin syndrome 2		HP:0001597	PMID:16380904	PCS		0/6			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609796	Peeling skin syndrome 2		HP:0040189	PMID:16380904	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-14]
OMIM:609796	Peeling skin syndrome 2		HP:0000007	PMID:16380904	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609796	Peeling skin syndrome 2		HP:0010783	PMID:16380904	PCS		6/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-14]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0002553	PMID:18179902	PCS		4/5			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000175	PMID:18179902	PCS		1/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0001660	PMID:18179902	PCS		1/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000430	PMID:18179902	PCS		4/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0004322	PMID:18179902	PCS		HP:0040282			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000490	PMID:18179902	PCS		3/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0001263	PMID:18179902	PCS		4/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000272	PMID:18179902	PCS		HP:0040282			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000708	PMID:18179902	PCS		2/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000319	PMID:18179902	PCS		6/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0030680	PMID:18179902	PCS		2/6			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000307	PMID:18179902	PCS		3/5			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0000219	PMID:18179902	PCS		HP:0040282			P	HPO:iea[2010-09-06]
OMIM:611867	Chromosome 22q11.2 deletion syndrome, distal		HP:0001511	PMID:18179902	PCS		5/6			P	HPO:iea[2010-09-06]
OMIM:167200	Pachyonychia congenita, type 1		HP:0001805	OMIM:167200	IEA					P	HPO:iea[2009-02-17]
OMIM:167200	Pachyonychia congenita, type 1		HP:0000972	PMID:7539673	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:167200	Pachyonychia congenita, type 1		HP:0008404	PMID:7539673	PCS		1/1			P	HPO:probinson[2022-09-01];HPO:probinson[2022-09-01]
OMIM:167200	Pachyonychia congenita, type 1		HP:0002745	PMID:7539673	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-01]
OMIM:167200	Pachyonychia congenita, type 1		HP:0007502	OMIM:167200	IEA					P	HPO:iea[2009-02-17]
OMIM:167200	Pachyonychia congenita, type 1		HP:0000006	PMID:7539673	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:620462	Cardiomyopathy, dilated, 2I		HP:0003621	PMID:30518548	PCS		1/2			C	HPO:probinson[2024-03-10]
OMIM:620462	Cardiomyopathy, dilated, 2I		HP:0011463	PMID:30518548	PCS		1/2			C	HPO:probinson[2024-03-10]
OMIM:620462	Cardiomyopathy, dilated, 2I		HP:0000007	PMID:30518548	PCS					I	HPO:probinson[2024-03-10]
OMIM:620462	Cardiomyopathy, dilated, 2I		HP:0012666	PMID:30518548	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:620462	Cardiomyopathy, dilated, 2I		HP:0004755	PMID:30518548	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:620462	Cardiomyopathy, dilated, 2I		HP:0001644	PMID:30518548;PMID:33083013	PCS		5/5			P	HPO:probinson[2024-03-10]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0000175	OMIM:243440	IEA					P	HPO:iea[2009-02-17]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0009892	OMIM:243440	TAS					P	HPO:skoehler[2013-05-31]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0008551	OMIM:243440	IEA					P	HPO:iea[2009-02-17]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0000932	OMIM:243440	IEA					P	HPO:iea[2009-02-17]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0000007	OMIM:243440	IEA					I	HPO:iea[2009-02-17]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0000238	OMIM:243440	IEA					P	HPO:iea[2009-02-17]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0000347	OMIM:243440	IEA					P	HPO:iea[2009-02-17]
OMIM:243440	Isotretinoin embryopathy-like syndrome		HP:0001710	OMIM:243440	IEA					P	HPO:iea[2009-02-17]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0000032	PMID:34202084	PCS		0/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0003251	PMID:34202084	PCS		2/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0012207	PMID:34202084	PCS		1/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0033525	PMID:34202084	PCS		2/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0032559	PMID:34202084	PCS		2/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0032560	PMID:34202084	PCS		2/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0034011	PMID:34202084	PCS		2/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0011462	PMID:34202084	PCS		2/2			C	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0032561	PMID:34202084	PCS		2/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0002837	PMID:34202084	PCS		0/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0000403	PMID:34202084	PCS		0/2			P	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0001417	PMID:34202084	PCS					I	HPO:probinson[2023-07-06]
OMIM:301101	Spermatogenic failure, X-linked, 6		HP:0006532	PMID:34202084	PCS		0/2			P	HPO:probinson[2023-07-06]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0003621	PMID:24292273	PCS		2/24			C	HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0003596	PMID:24292273	PCS		3/24			C	HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0006518	PMID:24292273	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0002094	PMID:24135949	PCS		4/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0025180	PMID:24292273	PCS		15/16			P	HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0012735	PMID:24135949	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0002092	PMID:24292273	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0045051	PMID:24292273;PMID:24135949	PCS		17/19			P	HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0100721	PMID:24292273	PCS		11/16			P	HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0012432	PMID:24135949	PCS		2/4			P	HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0011462	PMID:24292273	PCS		19/24			C	HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0000007	PMID:24292273	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2020-10-21]
OMIM:234810	Pulmonary venoocclusive disease 2		HP:0005954	PMID:24292273	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2020-10-21]
OMIM:613080	46XY sex reversal 5		HP:0000055	PMID:19361780	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-14]
OMIM:613080	46XY sex reversal 5		HP:0003577	PMID:19361780	PCS		1/1			C	HPO:probinson[2024-03-14]
OMIM:613080	46XY sex reversal 5		HP:0012245	PMID:19361780	PCS		1/1			P	HPO:probinson[2018-03-07];HPO:probinson[2024-03-14]
OMIM:613080	46XY sex reversal 5		HP:0030345	PMID:19361780	PCS		0/1			P	HPO:probinson[2015-12-30];HPO:probinson[2024-03-14]
OMIM:613080	46XY sex reversal 5		HP:0008232	PMID:19361780	PCS		1/1			P	HPO:probinson[2015-12-30];HPO:probinson[2024-03-14]
OMIM:613080	46XY sex reversal 5		HP:0000007	PMID:19361780	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-14]
OMIM:613080	46XY sex reversal 5		HP:0011731	PMID:19361780	PCS		0/1			P	HPO:probinson[2024-03-14]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0002069	PMID:21820099	PCS	HP:0011462	1/1			P	HPO:probinson[2022-09-24]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0002367	OMIM:162350	TAS					P	HPO:probinson[2012-06-11]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0001300	OMIM:162350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0001250	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0002074	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0001251	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0032794	PMID:21820099	PCS	HP:0011462	1/1			P	HPO:probinson[2022-09-24]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0002071	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0000716	PMID:21820099	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0000726	PMID:21820099	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0011462	PMID:21820099	PCS		1/1			C	HPO:probinson[2022-09-24]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0001317	OMIM:162350	IEA					P	HPO:skoehler[2018-10-08]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0003208	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0008765	OMIM:162350	TAS					P	HPO:probinson[2012-06-11]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0003657	PMID:21820099	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-24]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0003226	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0000006	PMID:21820099	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0003678	OMIM:162350	IEA					C	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0001336	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:162350	Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant		HP:0003205	OMIM:162350	IEA					P	HPO:iea[2009-02-17]
OMIM:614937	Myoclonus, familial cortical		HP:0034360	PMID:22926851	PCS		11/11			P	HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0002345	PMID:22926851	PCS		1/11			P	HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0100785	PMID:22926851	PCS		10/11			P	HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0003596	PMID:22926851	PCS		5/11			C	HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0003584	PMID:22926851	PCS		1/11			C	HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0011462	PMID:22926851	PCS		5/11			C	HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0001251	PMID:22926851	PCS		4/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0002359	PMID:22926851	PCS		8/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0000006	PMID:22926851	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0003677	PMID:22926851	PCS					C	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-11]
OMIM:614937	Myoclonus, familial cortical		HP:0001336	PMID:22926851	PCS					P	HPO:skoehler[2013-01-21];HPO:probinson[2023-03-11]
OMIM:615397	Meckel syndrome 11		HP:0001562	PMID:23349226	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-01-26]
OMIM:615397	Meckel syndrome 11		HP:0003577	PMID:23349226	PCS		1/1			C	HPO:probinson[2023-01-26]
OMIM:615397	Meckel syndrome 11		HP:0002085	PMID:23349226	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-01-26]
OMIM:615397	Meckel syndrome 11		HP:0000007	PMID:23349226	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-01-26]
OMIM:615397	Meckel syndrome 11		HP:0010442	PMID:23349226	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-01-26]
OMIM:615397	Meckel syndrome 11		HP:0000113	PMID:23349226	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-01-26]
OMIM:614089	Atrial septal defect 3		HP:0001684	PMID:15735645	PCS					P	HPO:probinson[2013-02-22]
OMIM:614089	Atrial septal defect 3		HP:0000006	PMID:15735645	PCS					I	HPO:probinson[2013-01-09]
OMIM:621032	Cerebral cavernous malformations 5		HP:0003621	PMID:33729480	PCS					C	HPO:probinson[2025-09-23]
OMIM:621032	Cerebral cavernous malformations 5		HP:0001442	PMID:33729480	PCS					I	HPO:probinson[2025-09-23]
OMIM:621032	Cerebral cavernous malformations 5		HP:0003581	PMID:33729480	PCS					C	HPO:probinson[2025-09-23]
OMIM:621032	Cerebral cavernous malformations 5		HP:0033522	PMID:33729480	PCS		43/43			P	HPO:probinson[2025-09-23]
OMIM:621032	Cerebral cavernous malformations 5		HP:0002170	PMID:33729480	PCS		11/43			P	HPO:probinson[2025-09-23]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003323	PMID:25938801	PCS					P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0001771	PMID:25938801	PCS					P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003202	PMID:25938801	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0001265	PMID:25938801	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0010628	PMID:25938801	PCS					P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003687	PMID:25938801	PCS					P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0002650	PMID:25938801	PCS		0/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003691	PMID:25938801	PCS		9/11			P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0001284	PMID:25938801	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003593	PMID:25938801	PCS					C	HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0031189	PMID:25938801	PCS		10/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0009130	PMID:25938801	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0009025	PMID:25938801	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0011462	PMID:25938801	PCS					C	HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0009027	PMID:25938801	PCS					P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003307	OMIM:616852	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0000006	PMID:25938801	PCS					I	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0001315	PMID:25938801	PCS					P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003798	PMID:25938801	PCS		0/5			P	HPO:probinson[2017-06-21];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003677	PMID:25938801	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-01]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003557	PMID:25938801	PCS					P	HPO:probinson[2017-06-21]
OMIM:616852	Myopathy, scapulohumeroperoneal		HP:0003722	PMID:25938801	PCS		12/12			P	HPO:probinson[2017-06-21]
OMIM:222900	Sucrase-isomaltase deficiency, congenital		HP:0002014	PMID:10903344	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:222900	Sucrase-isomaltase deficiency, congenital		HP:0002024	OMIM:222900	IEA					P	HPO:iea[2009-02-17]
OMIM:222900	Sucrase-isomaltase deficiency, congenital		HP:0003593	PMID:10903344	PCS		1/1			C	HPO:probinson[2021-01-30]
OMIM:222900	Sucrase-isomaltase deficiency, congenital		HP:0000007	PMID:8609217	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:222900	Sucrase-isomaltase deficiency, congenital		HP:0033597	OMIM:222900	TAS					P	HPO:probinson[2021-02-13]
OMIM:222900	Sucrase-isomaltase deficiency, congenital		HP:0000787	OMIM:222900	IEA					P	HPO:iea[2009-02-17]
OMIM:222900	Sucrase-isomaltase deficiency, congenital		HP:0002027	PMID:16329100	PCS					P	HPO:probinson[2021-01-30]
OMIM:400044	46XY sex reversal 1		HP:0000055	OMIM:400044	IEA					P	HPO:skoehler[2013-01-09]
OMIM:400044	46XY sex reversal 1		HP:0000032	OMIM:400044	IEA					P	HPO:skoehler[2013-01-09]
OMIM:400044	46XY sex reversal 1		HP:0000098	OMIM:400044	IEA					P	HPO:skoehler[2013-01-09]
OMIM:400044	46XY sex reversal 1		HP:0000133	OMIM:400044	IEA					P	HPO:skoehler[2013-01-09]
OMIM:400044	46XY sex reversal 1		HP:0000062	PMID:12793612	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2020-07-24]
OMIM:400044	46XY sex reversal 1		HP:0000150	OMIM:400044	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400044	46XY sex reversal 1		HP:0011969	PMID:2247151	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-08]
OMIM:400044	46XY sex reversal 1		HP:0001450	PMID:12793612	PCS					I	HPO:probinson[2020-07-24]
OMIM:400044	46XY sex reversal 1		HP:0000140	OMIM:400044	IEA					P	HPO:skoehler[2013-01-09]
OMIM:400044	46XY sex reversal 1		HP:0012245	PMID:2247151	PCS		1/1			P	HPO:skoehler[2013-04-04];HPO:probinson[2023-04-08]
OMIM:400044	46XY sex reversal 1		HP:0008187	OMIM:400044	IEA					P	HPO:skoehler[2013-01-09]
OMIM:400044	46XY sex reversal 1		HP:0000815	PMID:2247151	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:400044	46XY sex reversal 1		HP:0008232	PMID:2247151	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-08]
OMIM:400044	46XY sex reversal 1		HP:0008723	PMID:2247151	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:400044	46XY sex reversal 1		HP:0000037	OMIM:400044	IEA					P	HPO:skoehler[2013-01-09]
OMIM:400044	46XY sex reversal 1		HP:0000786	OMIM:400044	IEA		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-04-08]
OMIM:613094	Microphthalmia, isolated 4		HP:0100259	PMID:19129173	PCS		1/3			P	HPO:iea[2012-04-24]
OMIM:613094	Microphthalmia, isolated 4		HP:0000568	PMID:19129173	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:613094	Microphthalmia, isolated 4		HP:0000006	PMID:19129173	PCS					I	HPO:iea[2012-04-24]
OMIM:613094	Microphthalmia, isolated 4		HP:0010469	PMID:19129173	PCS					P	HPO:iea[2012-04-24]
OMIM:613094	Microphthalmia, isolated 4		HP:0000589	PMID:19129173	PCS		1/3			P	HPO:iea[2012-04-24]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0001410	OMIM:602199	IEA					P	HPO:iea[2009-02-17]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0002013	OMIM:602199	IEA					P	HPO:iea[2009-02-17]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0003201	OMIM:602199	IEA					P	HPO:iea[2009-02-17]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0001944	OMIM:602199	IEA					P	HPO:iea[2009-02-17]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0002913	OMIM:602199	IEA					P	HPO:iea[2009-02-17]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0000007	OMIM:602199	IEA					I	HPO:iea[2009-02-17]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0003811	OMIM:602199	IEA					C	HPO:iea[2009-02-17]
OMIM:602199	Medium chain 3-ketoacyl-coa thiolase deficiency		HP:0001942	OMIM:602199	IEA					P	HPO:iea[2009-02-17]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002069	PMID:36729635;PMID:22956686	PCS		4/19			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002463	PMID:36729635	PCS		17/17			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001332	PMID:36729635	PCS		2/10			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001250	PMID:36729635;PMID:22956686	PCS		11/25			P	HPO:skoehler[2013-01-11];HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001252	PMID:36729635	PCS		5/17			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001251	PMID:36729635	PCS		1/20			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0003593	PMID:22956686	PCS		4/6			C	ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0011182	PMID:36729635;PMID:22956686	PCS		17/24			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000518	PMID:22956686	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000958	PMID:36729635	PCS		2/17			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0011463	PMID:22956686	PCS		2/6			C	ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000718	PMID:36729635	PCS		8/18			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000717	PMID:36729635	PCS		11/19			P	HPO:skoehler[2013-01-09];HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000711	PMID:36729635	PCS		6/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000752	PMID:36729635	PCS		5/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001249	PMID:36729635;PMID:22956686	PCS		22/22			P	HPO:skoehler[2013-01-11];HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000253	PMID:36729635	PCS		17/20			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002312	PMID:36729635	PCS		12/15			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000252	PMID:22956686	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0011968	PMID:36729635	PCS		5/20			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000293	PMID:36729635	PCS		4/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002197	PMID:36729635	PCS		9/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001263	PMID:36729635;PMID:22956686	PCS		27/27			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0500194	PMID:36729635	PCS		20/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0011171	PMID:22956686	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0500190	PMID:36729635	PCS		19/21			P	HPO:probinson[2024-04-27];HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000407	PMID:36729635	PCS		3/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000729	PMID:36729635;PMID:22956686	PCS		20/25			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000007	PMID:22956686	PCS					I	ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0007359	PMID:36729635	PCS		1/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000126	PMID:36729635	PCS		1/17			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002487	PMID:36729635	PCS		1/20			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002123	PMID:36729635	PCS		1/18			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001271	PMID:36729635	PCS		2/17			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001270	PMID:36729635;PMID:22956686	PCS		26/26			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0011123	PMID:36729635	PCS		3/17			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000219	PMID:36729635	PCS		4/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0500188	PMID:36729635	PCS		20/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0500144	PMID:36729635;PMID:22956686	PCS		25/27			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0500143	PMID:36729635;PMID:22956686	PCS		26/27			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001347	PMID:36729635;PMID:22956686	PCS		7/19			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0005326	PMID:36729635	PCS		2/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002376	PMID:36729635	PCS		5/8			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000350	PMID:36729635	PCS		3/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0005484	PMID:36729635	PCS		16/20			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0011147	PMID:36729635	PCS		2/18			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0001999	PMID:36729635	PCS		10/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0002208	PMID:36729635	PCS		1/17			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0000422	PMID:36729635	PCS		2/21			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0007018	PMID:36729635	PCS		4/18			P	HPO:probinson[2024-04-27]
OMIM:614923	Branched-chain keto acid dehydrogenase kinase deficiency		HP:0500132	PMID:36729635;PMID:22956686	PCS		26/27			P	HPO:probinson[2024-04-27];ORCID:0000-0002-0736-9199[2024-04-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000750	PMID:17333282	PCS		1/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0001250	OMIM:309549	IEA		HP:0040283			P	HPO:skoehler[2013-01-09]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0001263	PMID:17333282	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0003593	PMID:15162322	PCS					C	HPO:probinson[2022-04-05]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0002194	PMID:17333282	PCS		1/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0005280	PMID:17333282	PCS		1/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0100753	PMID:15162322	PCS		1/14			P	HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0001419	PMID:15162322	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0011463	PMID:15162322	PCS					C	HPO:probinson[2022-04-05]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000718	PMID:15162322	PCS		5/14			P	HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000629	OMIM:309549	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000717	PMID:17333282	PCS	HP:0003593	1/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000739	PMID:15162322	PCS		2/14			P	HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0009882	PMID:17333282	PCS		1/3			P	HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000637	OMIM:309549	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000400	PMID:8288232	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0000179	OMIM:309549	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309549	Intellectual developmental disorder, X-linked 9		HP:0001249	PMID:15162322	PCS		14/14			P	HPO:probinson[2021-09-27]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0004313	PMID:37875108	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0020086	PMID:37875108	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0011463	PMID:37875108	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0001419	PMID:37875108	PCS					I	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0001263	PMID:37875108	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0002240	PMID:37875108	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0020087	PMID:37875108	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0003593	PMID:37875108	PCS		4/5			C	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0001954	PMID:37875108	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0002716	PMID:37875108	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0001744	PMID:37875108	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:301115	Immunodeficiency 118, mycobacteriosis		HP:0002754	PMID:37875108	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:615382	Nephronophthisis 16		HP:0001650	PMID:23793029	PCS		4/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0003774	PMID:23793029	PCS		6/7			P	HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0001396	PMID:23793029	PCS		1/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0003577	PMID:23793029	PCS		1/7			C	HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0003621	PMID:23793029	PCS		3/7			C	HPO:probinson[2022-09-27];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0001696	PMID:23793029	PCS		1/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0000083	PMID:23793029	PCS		7/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0003593	PMID:23793029	PCS		1/7			C	HPO:probinson[2022-09-27];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0000090	PMID:23793029	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0011463	PMID:23793029	PCS		2/7			C	HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0001639	PMID:23793029	PCS		1/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0001405	PMID:23793029	PCS		1/7			P	HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0000007	PMID:23793029	PCS					I	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0001643	PMID:23793029	PCS		1/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0000113	PMID:23793029	PCS		7/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0001642	PMID:23793029	PCS		1/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:615382	Nephronophthisis 16		HP:0000105	PMID:23793029	PCS		4/7			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-09-27]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0001254	OMIM:201100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0004322	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0003593	PMID:31987033	PCS		25/27			C	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0002240	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0001251	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0033194	PMID:31987033	PCS		2/2			P	HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0033195	PMID:31987033	PCS	HP:0011463	2/2			P	HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0001508	PMID:31987033	PCS		8/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0000958	PMID:31987033	PCS		2/2			P	HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0000737	OMIM:201100	TAS					P	HPO:probinson[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0011463	PMID:31987033	PCS		2/27			C	HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0000712	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0008734	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0000135	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0001744	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0002014	PMID:31987033	PCS		12/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0005401	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0004396	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0003282	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0040171	OMIM:201100	TAS			MALE		P	HP:probinson[2019-04-12]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0002293	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0011840	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0031831	PMID:31987033	PCS		19/24		HP:4000103	P	HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0001818	OMIM:201100	IEA					P	HPO:iea[2009-02-17]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0000007	PMID:12068297	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0000224	OMIM:201100	TAS					P	HPO:probinson[2012-07-16]
OMIM:201100	Acrodermatitis enteropathica, Zinc-Deficiency type		HP:0001337	OMIM:201100	TAS					P	HPO:probinson[2009-02-17]
OMIM:400045	46XX sex reversal 1		HP:0000098	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0012245	OMIM:400045	TAS					P	HPO:probinson[2013-04-04]
OMIM:400045	46XX sex reversal 1		HP:0000771	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0012861	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0011969	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0008232	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0000813	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0008665	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0001423	OMIM:400045	TAS					I	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0010459	OMIM:400045	TAS					P	HPO:probinson[2013-04-04]
OMIM:400045	46XX sex reversal 1		HP:0000047	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400045	46XX sex reversal 1		HP:0000027	OMIM:400045	IEA					P	HPO:skoehler[2019-09-07]
OMIM:177990	Pterygium colli, isolated		HP:0000286	OMIM:177990	IEA					P	HPO:iea[2009-02-17]
OMIM:177990	Pterygium colli, isolated		HP:0002162	OMIM:177990	IEA					P	HPO:iea[2009-02-17]
OMIM:177990	Pterygium colli, isolated		HP:0003196	OMIM:177990	IEA					P	HPO:iea[2009-02-17]
OMIM:177990	Pterygium colli, isolated		HP:0000411	OMIM:177990	IEA					P	HPO:iea[2009-02-17]
OMIM:177990	Pterygium colli, isolated		HP:0000465	OMIM:177990	IEA					P	HPO:iea[2009-02-17]
OMIM:177990	Pterygium colli, isolated		HP:0000006	OMIM:177990	IEA					I	HPO:iea[2009-02-17]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000582	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001531	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000486	PMID:28334855	PCS		3/3			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001332	PMID:28334855;PMID:34716203	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000089	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001970	PMID:28334855	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001195	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000083	PMID:28334855	PCS	HP:0011463	4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001274	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0003593	PMID:28334855	PCS		2/6			C	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0012625	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0012389	PMID:34716203	PCS		0/1			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0100595	PMID:28334855;PMID:34716203	PCS		6/7			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0011463	PMID:28334855	PCS		3/6			C	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0100702	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0011461	PMID:34716203	PCS		1/1			C	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0004719	PMID:28334855	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000657	PMID:28334855	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001302	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0008936	PMID:28334855;PMID:34716203	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000297	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0003621	PMID:28334855	PCS		1/6			C	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000252	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000750	PMID:28334855	PCS		6/6			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001266	PMID:28334855	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0002376	PMID:28334855	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001288	PMID:34716203	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0011968	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0002153	PMID:28334855	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001263	PMID:28334855	PCS		6/6			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0002070	PMID:28334855	PCS		6/6			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0011344	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0100660	PMID:28334855	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000408	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0032232	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0002509	PMID:28334855;PMID:34716203	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000508	PMID:28334855	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000822	PMID:28334855	PCS		4/4			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000007	PMID:28334855	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000527	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0000648	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001511	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0001510	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:617595	Birk-Landau-Perez syndrome		HP:0002643	PMID:34716203	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:205400	Tangier disease		HP:0003477	OMIM:205400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:205400	Tangier disease		HP:0007759	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0003233	PMID:10431236	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2022-10-10]
OMIM:205400	Tangier disease		HP:0003693	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0002164	OMIM:205400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:205400	Tangier disease		HP:0010829	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0002240	OMIM:205400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:205400	Tangier disease		HP:0031800	PMID:10431236	PCS					P	HPO:probinson[2022-10-10]
OMIM:205400	Tangier disease		HP:0000958	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0000656	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0001349	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0001744	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0007328	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0001265	OMIM:205400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:205400	Tangier disease		HP:0002155	PMID:10431236	PCS					P	HPO:probinson[2022-10-10]
OMIM:205400	Tangier disease		HP:0031799	PMID:10431236	PCS					P	HPO:probinson[2022-10-10]
OMIM:205400	Tangier disease		HP:0011096	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0025608	OMIM:205400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:205400	Tangier disease		HP:0001658	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0000007	PMID:10431236	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-10-10]
OMIM:205400	Tangier disease		HP:0001712	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0000505	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0008404	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0002621	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:205400	Tangier disease		HP:0001677	OMIM:205400	PCS					P	HPO:probinson[2012-04-11]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0000494	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0003577	PMID:36927955	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0001520	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0002343	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0002002	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0000490	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0002240	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0001548	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0001417	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0006610	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0000411	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0000256	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0001763	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0001744	PMID:36927955	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:301114	Lui-Jee-Baron syndrome		HP:0001249	PMID:36927955	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000286	OMIM:309548	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0002311	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000252	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000750	PMID:8651274	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0004322	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0100023	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0100710	OMIM:309548	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0012172	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0001419	PMID:8334699	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000718	PMID:8651274	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0001609	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0011341	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0012471	PMID:8651274	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000426	OMIM:309548	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000722	OMIM:309548	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000713	OMIM:309548	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0025116	PMID:8651274	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0000752	OMIM:309548	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0001511	PMID:8651274	PCS	HP:0011461	2/4			P	HPO:probinson[2021-10-02]
OMIM:309548	Intellectual developmental disorder, X-linked 109		HP:0001249	PMID:8334699;PMID:8651274	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:248500	Alpha-mannosidosis		HP:0000286	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0002980	OMIM:248500	TAS					P	HPO:skoehler[2013-10-22]
OMIM:248500	Alpha-mannosidosis		HP:0002066	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001252	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001290	OMIM:248500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:248500	Alpha-mannosidosis		HP:0000280	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000639	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000998	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001922	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000158	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001249	OMIM:248500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:248500	Alpha-mannosidosis		HP:0005469	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000574	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0003487	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001260	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001263	OMIM:248500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248500	Alpha-mannosidosis		HP:0000294	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0004570	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0011800	OMIM:248500	TAS					P	HPO:skoehler[2013-11-28]
OMIM:248500	Alpha-mannosidosis		HP:0002070	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000407	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0007232	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000007	OMIM:248500	IEA					I	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0005619	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000768	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000400	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001257	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000687	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000023	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0002684	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001272	PMID:33317989	IEA		8/13			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:248500	Alpha-mannosidosis		HP:0002120	PMID:33317989	PCS		8/13			P	HPO:probinson[2021-07-02]
OMIM:248500	Alpha-mannosidosis		HP:0002240	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0012448	OMIM:248500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:248500	Alpha-mannosidosis		HP:0002280	PMID:33317989	PCS		11/13			P	HPO:probinson[2021-07-02]
OMIM:248500	Alpha-mannosidosis		HP:0034712	OMIM:248500	TAS		20/20			P	HPO:probinson[2023-06-05];HPO:probinson[2024-01-06]
OMIM:248500	Alpha-mannosidosis		HP:4000190	OMIM:248500	TAS					P	HPO:probinson[2024-01-06]
OMIM:248500	Alpha-mannosidosis		HP:0002718	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001547	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000337	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000212	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000256	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000457	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001744	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0001347	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0004313	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0003302	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000272	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0002171	OMIM:248500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:248500	Alpha-mannosidosis		HP:0007371	PMID:33317989	PCS		3/13			P	HPO:probinson[2021-07-02]
OMIM:248500	Alpha-mannosidosis		HP:0000943	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0007772	OMIM:248500	IEA	HP:0003581				P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0007256	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000546	PMID:15534274	TAS	HP:0003581			HP:0003676	P	HP:probinson[2018-05-07]
OMIM:248500	Alpha-mannosidosis		HP:0002007	OMIM:248500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248500	Alpha-mannosidosis		HP:0001510	OMIM:248500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:248500	Alpha-mannosidosis		HP:0000303	OMIM:248500	IEA					P	HPO:iea[2009-02-17]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001254	PMID:23022099	PCS		2/5			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001397	OMIM:614922	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0003577	PMID:23022099	PCS		5/5			C	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0000365	OMIM:614922	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001410	OMIM:614922	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0000089	OMIM:614922	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001250	OMIM:614922	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0003198	OMIM:614922	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0002120	OMIM:614922	TAS					P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0000083	PMID:23022099	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0006829	OMIM:614922	TAS					P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0002240	OMIM:614922	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001290	PMID:23022099	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0012448	OMIM:614922	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001947	OMIM:614922	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0003826	PMID:23022099	PCS		1/5			C	HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001308	PMID:23022099	PCS		2/5			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0002878	PMID:23022099	PCS	HP:0003623	5/5			P	HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0003429	OMIM:614922	TAS					P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001302	OMIM:614922	TAS					P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001522	PMID:23022099;OMIM:614922	PCS		12/15			C	HPO:probinson[2023-06-04];HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0003128	PMID:23022099	PCS		4/4			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0000110	OMIM:614922	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001265	PMID:23022099	PCS		2/5			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001561	PMID:23022099	PCS		2/5			P	HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001344	OMIM:614922	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0002079	OMIM:614922	TAS					P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0011968	OMIM:614922	TAS					P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0002151	PMID:23022099	PCS		4/4			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001263	OMIM:614922	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001284	PMID:23022099	PCS		1/5			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0002490	OMIM:614922	TAS					P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0003819	PMID:23022099	PCS		1/5			C	HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0000107	OMIM:614922	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0009830	OMIM:614922	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0000007	PMID:23022099	PCS					I	HPO:skoehler[2012-11-25];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001638	OMIM:614922	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0003811	PMID:23022099	PCS		1/5			C	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:614922	Combined oxidative phosphorylation deficiency 11		HP:0001336	OMIM:614922	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:613095	Polycystic kidney disease 2		HP:0003774	PMID:35447873	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0003621	PMID:16430766	PCS		2/3			C	HPO:probinson[2022-03-16]
OMIM:613095	Polycystic kidney disease 2		HP:0003676	PMID:35447873	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0000010	OMIM:613095	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613095	Polycystic kidney disease 2		HP:0003596	PMID:16430766	PCS		1/3			C	HPO:probinson[2022-03-16]
OMIM:613095	Polycystic kidney disease 2		HP:0001696	PMID:35447873	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0001651	OMIM:613095	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613095	Polycystic kidney disease 2		HP:0003155	PMID:35447873	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0000083	OMIM:613095	TAS					P	HPO:probinson[2013-06-02]
OMIM:613095	Polycystic kidney disease 2		HP:0005562	PMID:35447873	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0002240	PMID:35447873	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0011800	OMIM:613095	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613095	Polycystic kidney disease 2		HP:0030948	PMID:35447873	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0011462	PMID:35447873	PCS		1/1			C	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0003829	OMIM:613095	TAS					I	HPO:skoehler[2017-07-13]
OMIM:613095	Polycystic kidney disease 2		HP:0006254	PMID:35447873	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0000822	PMID:16430766	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:613095	Polycystic kidney disease 2		HP:0001407	PMID:35447873;PMID:34749493;PMID:16430766	PCS		6/8			P	HPO:probinson[2022-03-16];HPO:probinson[2022-06-20];HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:613095	Polycystic kidney disease 2		HP:0002900	PMID:35447873	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0000113	PMID:34749493;PMID:16430766	PCS		7/7			P	HPO:probinson[2022-03-16];HPO:probinson[2013-06-02];HPO:probinson[2022-03-16]
OMIM:613095	Polycystic kidney disease 2		HP:0000006	PMID:8650545	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-03-16]
OMIM:613095	Polycystic kidney disease 2		HP:0003259	PMID:34749493;PMID:16430766	PCS		1/7			P	HPO:probinson[2022-03-16];HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:613095	Polycystic kidney disease 2		HP:0000952	PMID:35447873	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:613095	Polycystic kidney disease 2		HP:0000324	OMIM:613095	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614936	Keratoderma, palmoplantar, punctate type IB		HP:0007530	PMID:22972947	PCS					P	HPO:probinson[2021-07-13]
OMIM:614936	Keratoderma, palmoplantar, punctate type IB		HP:0000006	PMID:22972947	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2021-07-13]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0001133	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0002069	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000662	PMID:7977353	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0004322	PMID:7977353	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000580	PMID:7977353	PCS		2/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0031624	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000518	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0011463	PMID:7977353	PCS		5/5			C	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000618	PMID:7977353	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000510	PMID:7977353	PCS	HP:0003593	5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0007787	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0007843	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0005328	PMID:7977353	PCS		2/5			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0001249	PMID:7977353	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000550	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0001583	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000252	PMID:7977353	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0002099	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0001263	PMID:7977353	PCS		5/5			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000708	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0001419	PMID:16419135	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000505	PMID:7977353	PCS		5/5	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000648	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000666	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:300578	Chromosome xp11.3 deletion syndrome		HP:0000028	PMID:7977353	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002663	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002982	OMIM:241530	TAS					P	HPO:probinson[2012-05-01]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0003698	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0003013	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002980	OMIM:241530	TAS					P	HPO:probinson[2012-05-01]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0003155	PMID:16358215	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0004363	PMID:16358215	PCS		0/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0001252	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0003593	OMIM:241530	IEA					C	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0010502	OMIM:241530	TAS					P	HPO:probinson[2012-05-01]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0001508	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002979	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0000117	PMID:16358215	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002757	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0004912	PMID:16358215	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0001324	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002753	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0003029	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0005469	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002653	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002752	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0000893	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0001288	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0003025	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0031817	PMID:16358215	PCS		3/4			P	HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0003020	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002150	PMID:16358215	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0004492	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0031414	PMID:16358215	PCS		0/5			P	HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0031415	PMID:16358215	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002748	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0000007	PMID:16358215	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0000920	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002007	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0004724	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0001510	OMIM:241530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0000124	OMIM:241530	TAS					P	HPO:skoehler[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0000886	OMIM:241530	IEA					P	HPO:iea[2009-02-17]
OMIM:241530	Hypophosphatemic rickets with hypercalciuria, hereditary		HP:0002148	PMID:16358215	PCS		7/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-10]
OMIM:615396	Left ventricular noncompaction 10		HP:0003584	PMID:21551322	PCS		1/6			C	HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0011462	PMID:21551322	IEA		5/6			C	HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0030682	PMID:21551322	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0001635	PMID:21551322	PCS		1/6			P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0002092	PMID:21551322	PCS		1/6			P	HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0033755	PMID:21551322	PCS		1/6			P	HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0001279	PMID:21551322	PCS		1/6			P	HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0000006	PMID:21551322	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2022-07-04]
OMIM:615396	Left ventricular noncompaction 10		HP:0001644	OMIM:615396	TAS					P	HPO:skoehler[2013-09-30]
OMIM:305400	Aarskog-Scott syndrome		HP:0000486	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0001773	OMIM:305400	TAS					P	HPO:probinson[2013-04-08]
OMIM:305400	Aarskog-Scott syndrome		HP:0004322	PMID:20082460;PMID:11093277;PMID:23211637	PCS		16/16			P	ORCID:0000-0002-0736-9199[2024-08-13];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0003311	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0003196	PMID:20082460;PMID:11093277;PMID:23211637	PCS		14/16			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0004482	PMID:11093277	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0032277	PMID:8076412	PCS		3/5			P	HP:probinson[2019-02-12]
OMIM:305400	Aarskog-Scott syndrome		HP:0011463	PMID:11093277	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000954	PMID:20082460;PMID:11093277	PCS		6/13			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000316	PMID:20082460;PMID:11093277;PMID:23211637;PMID:34189097	PCS		17/17			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:probinson[2021-07-05];HPO:iea[2009-02-17];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0009466	OMIM:305400	IEA					P	HPO:iea[2009-02-17];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0001769	PMID:20082460	PCS		8/11			P	HPO:probinson[2013-04-08];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000311	PMID:34189097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0001763	PMID:34189097	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0001840	PMID:20082460;PMID:23211637	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0001169	PMID:20082460	PCS		22/22			P	HPO:probinson[2013-04-07];HP:probinson[2018-09-23];ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0009748	OMIM:305400	IEA					P	HPO:iea[2009-02-17];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0001249	PMID:23211637	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0003502	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0000252	PMID:11093277	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0001187	PMID:20082460;PMID:34189097	PCS		3/12			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0000494	PMID:20082460;PMID:11093277	PCS		7/14			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000175	OMIM:305400	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0002750	PMID:20082460;PMID:11093277	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0001382	PMID:34189097	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0011969	PMID:34189097	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0001263	PMID:20082460;PMID:23211637	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-08-13];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0011800	PMID:20082460	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0012774	OMIM:305400	TAS					P	HPO:skoehler[2014-04-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0012385	PMID:20082460	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0001419	OMIM:305400	IEA					I	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0001537	PMID:20082460;PMID:11093277	PCS		3/14			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000767	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0000327	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0000689	PMID:20082460	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0003318	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0004209	PMID:20082460	PCS		8/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000047	PMID:20082460	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000289	PMID:20082460;PMID:11093277	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HP:probinson[2018-09-23];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0008689	PMID:34189097	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0000204	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0000049	PMID:20082460	PCS	HP:0003577	10/11			P	HPO:iea[2009-02-17];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0000049	PMID:34189097	PCS	HP:0003577	1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0000049	PMID:11093277	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000049	PMID:23211637	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000384	PMID:20082460	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000343	PMID:20082460	PCS		9/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000023	PMID:20082460;PMID:11093277	PCS		4/14			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HP:probinson[2018-09-23];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000540	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0001156	PMID:11093277;PMID:34189097	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0000463	PMID:20082460;PMID:11093277;PMID:23211637	PCS		14/16			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0001508	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0008232	PMID:34189097	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0000218	PMID:23211637	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0001544	PMID:8076412	PCS		2/5			P	HPO:iea[2009-02-17];HP:probinson[2019-02-12]
OMIM:305400	Aarskog-Scott syndrome		HP:0000431	PMID:34189097	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0004279	PMID:20082460	PCS		11/11			P	HPO:probinson[2013-04-07];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0002650	OMIM:305400	IEA					P	HPO:iea[2009-02-17];HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0002055	PMID:20082460	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000470	PMID:20082460	PCS		11/11			P	HPO:probinson[2009-02-17];HP:probinson[2018-09-23];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0040171	PMID:34189097	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0000508	PMID:20082460;PMID:11093277;PMID:23211637	PCS		9/16			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000349	PMID:20082460;PMID:11093277	PCS		9/14			P	ORCID:0000-0002-0736-9199[2024-08-13];HPO:iea[2009-02-17];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000668	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0000029	PMID:34189097	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:305400	Aarskog-Scott syndrome		HP:0000307	PMID:11093277	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0009237	PMID:20082460	PCS		8/11			P	HP:probinson[2018-09-23]
OMIM:305400	Aarskog-Scott syndrome		HP:0000823	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0001159	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0002007	PMID:20082460	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0007018	OMIM:305400	IEA					P	HPO:iea[2009-02-17]
OMIM:305400	Aarskog-Scott syndrome		HP:0001513	PMID:20082460	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000347	PMID:23211637	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000028	PMID:20082460	PCS	HP:0003577	6/11			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-28]
OMIM:305400	Aarskog-Scott syndrome		HP:0000028	PMID:11093277	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:305400	Aarskog-Scott syndrome		HP:0000028	PMID:23211637	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0000670	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0000890	OMIM:244460	TAS					P	HPO:probinson[2012-05-27]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0001476	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0001773	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0004279	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0002750	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0001250	OMIM:244460	IEA					P	HPO:skoehler[2010-06-20]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0003561	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0003100	OMIM:244460	TAS					P	HPO:probinson[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0004331	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0005450	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0001281	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0002917	OMIM:244460	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0008198	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0001903	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0002718	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0000316	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0000007	OMIM:244460	IEA					I	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0003508	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0002901	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0001511	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0200055	OMIM:244460	TAS					P	HPO:skoehler[2012-10-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0000883	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:244460	Kenny-caffey syndrome, type 1		HP:0006645	OMIM:244460	IEA					P	HPO:iea[2009-02-17]
OMIM:620305	Neurooculorenal syndrome		HP:0000486	PMID:30692597;PMID:35227688	PCS		4/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000122	PMID:35227688	PCS		4/8			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001651	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0012624	PMID:35227688	PCS		3/8			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0033725	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0012110	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001607	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0004719	PMID:35227688	PCS		5/6			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000238	PMID:30692597;PMID:29194579;PMID:35227688	PCS		3/11			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0008897	PMID:35227688	PCS		3/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001249	PMID:35227688	PCS		4/5			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0002553	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0010958	PMID:29194579;PMID:35227688	PCS		4/11			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0005343	PMID:29194579	PCS		1/3			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001263	PMID:35227688	PCS		4/5			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0008163	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0002908	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0034198	PMID:29194579	PCS		2/3			C	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000407	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000007	PMID:29194579	PCS					I	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001338	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001335	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13];HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000289	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001655	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0003774	PMID:35227688	PCS		1/8			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0003577	PMID:30692597	PCS		1/1			C	HPO:probinson[2023-07-13];HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0010109	PMID:29194579	PCS		2/3			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000540	PMID:35227688	PCS		1/5			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001274	PMID:29194579;PMID:35227688	PCS		2/10			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0011755	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0011679	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0010034	PMID:29194579	PCS		1/3			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001988	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000337	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0002119	PMID:29194579;PMID:35227688	PCS		2/10			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000410	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001545	PMID:29194579	PCS		2/3			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001089	PMID:35227688	PCS		1/5			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0002410	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001320	PMID:35227688	PCS		2/7			P	HPO:probinson[2023-07-13];HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001762	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0011787	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0025700	PMID:29194579	PCS		2/3			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0002920	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0002126	PMID:29194579	PCS		1/3			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0002566	PMID:29194579	PCS		2/3			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000028	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0000347	PMID:30692597	PCS		1/1			P	HPO:probinson[2023-07-13]
OMIM:620305	Neurooculorenal syndrome		HP:0001634	PMID:35227688	PCS		1/7			P	HPO:probinson[2023-07-13]
OMIM:304050	Aicardi syndrome		HP:0002389	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0002188	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0030731	OMIM:304050	IEA					P	HPO:skoehler[2018-10-08]
OMIM:304050	Aicardi syndrome		HP:0001250	OMIM:304050	PCS					P	HPO:probinson[2012-03-17]
OMIM:304050	Aicardi syndrome		HP:0001252	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0010609	OMIM:304050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:304050	Aicardi syndrome		HP:0001290	OMIM:304050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:304050	Aicardi syndrome		HP:0012469	OMIM:304050	TAS					P	HPO:skoehler[2013-11-28]
OMIM:304050	Aicardi syndrome		HP:0007082	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000518	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000639	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0002937	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0012032	OMIM:304050	TAS					P	HPO:skoehler[2012-11-18]
OMIM:304050	Aicardi syndrome		HP:0009623	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0008897	OMIM:304050	PCS					P	HPO:probinson[2012-03-17]
OMIM:304050	Aicardi syndrome		HP:0002414	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0003305	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000951	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0002036	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000175	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000252	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0010759	OMIM:304050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:304050	Aicardi syndrome		HP:0000892	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0002190	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0011097	OMIM:304050	PCS					P	HPO:probinson[2012-03-17]
OMIM:304050	Aicardi syndrome		HP:0002308	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000921	OMIM:304050	PCS					P	HPO:probinson[2012-03-17]
OMIM:304050	Aicardi syndrome		HP:0000568	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0001338	OMIM:304050	PCS					P	HPO:probinson[2012-03-17]
OMIM:304050	Aicardi syndrome		HP:0000648	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0005815	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0003316	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000204	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000324	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0005338	OMIM:304050	TAS					P	HPO:skoehler[2012-11-18]
OMIM:304050	Aicardi syndrome		HP:0002884	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0007858	OMIM:304050	PCS					P	HPO:probinson[2012-04-07]
OMIM:304050	Aicardi syndrome		HP:0000541	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000463	OMIM:304050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:304050	Aicardi syndrome		HP:0002282	OMIM:304050	TAS					P	HPO:skoehler[2012-11-18]
OMIM:304050	Aicardi syndrome		HP:0001305	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0006532	OMIM:304050	PCS					P	HPO:probinson[2012-03-17]
OMIM:304050	Aicardi syndrome		HP:0001302	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0001423	OMIM:304050	IEA					I	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0001028	OMIM:304050	TAS					P	HPO:skoehler[2012-11-18]
OMIM:304050	Aicardi syndrome		HP:0001320	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0006956	OMIM:304050	TAS					P	HPO:probinson[2012-06-10]
OMIM:304050	Aicardi syndrome		HP:0002650	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000826	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0000902	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:304050	Aicardi syndrome		HP:0009792	OMIM:304050	TAS					P	HPO:skoehler[2012-11-18]
OMIM:304050	Aicardi syndrome		HP:0200059	OMIM:304050	TAS					P	HPO:skoehler[2012-11-18]
OMIM:304050	Aicardi syndrome		HP:0002126	OMIM:304050	TAS					P	HPO:skoehler[2012-11-18]
OMIM:304050	Aicardi syndrome		HP:0000588	OMIM:304050	IEA					P	HPO:iea[2009-02-17]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001254	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001298	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0003236	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0003234	PMID:11715001	PCS		5/5			P	HPO:skoehler[2015-12-23];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0003198	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001252	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0002240	PMID:11715001	PCS		1/5			P	HPO:iea[2015-12-23];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001290	OMIM:212140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0031964	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001508	OMIM:212140	TAS					P	HPO:skoehler[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001706	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0011463	PMID:11715001	PCS		5/5			C	HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0030362	OMIM:212140	TAS					P	HPO:probinson[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001988	PMID:11715001	PCS		1/5			P	HPO:skoehler[2015-12-23];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001944	PMID:11715001	PCS		2/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001987	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001946	PMID:11715001	PCS		0/5			P	HPO:skoehler[2015-12-23];HPO:probinson[2024-03-08]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0003701	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001324	PMID:11715001;OMIM:212140	PCS		11/15			P	HPO:iea[2015-12-23];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0002014	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0045061	OMIM:212140	TAS					P	HPO:skoehler[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0031956	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001289	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0002013	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001640	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0002098	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001263	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001262	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001639	OMIM:212140	TAS					P	HPO:skoehler[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001635	OMIM:212140	TAS					P	HPO:skoehler[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0000007	PMID:9916797	PCS					I	HPO:probinson[2015-12-23];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0005959	OMIM:212140	IEA					P	HPO:iea[2015-12-23]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001638	PMID:11715001	PCS		2/5			P	HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001653	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001414	PMID:11715001	PCS		1/5			P	HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0003215	PMID:11715001	PCS		1/5			P	HPO:skoehler[2015-12-23];HPO:probinson[2022-10-09]
OMIM:212140	Carnitine deficiency, systemic primary		HP:0001259	PMID:11715001	PCS		2/5			P	HPO:iea[2015-12-23];HPO:probinson[2022-10-09]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0001761	OMIM:309560	IEA					P	HPO:iea[2009-02-17]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0001419	OMIM:309560	TAS					I	HPO:skoehler[2013-10-06]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0001417	OMIM:309560	IEA					I	HPO:iea[2009-02-17]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0000218	OMIM:309560	TAS					P	HPO:skoehler[2013-10-06]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0000972	OMIM:309560	IEA					P	HPO:iea[2009-02-17]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0001258	OMIM:309560	IEA					P	HPO:iea[2009-02-17]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0001249	OMIM:309560	IEA					P	HPO:iea[2009-02-17]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0001348	OMIM:309560	TAS					P	HPO:skoehler[2013-10-06]
OMIM:309560	Impaired intellectual development with spastic paraplegia and palmoplantar hyperkeratosis		HP:0001337	OMIM:309560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277900	Wilson disease		HP:0001332	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0003355	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0001250	PMID:33879678	PCS	HP:0003621	1/14			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002063	PMID:31426520	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0003076	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0003073	PMID:35169583;PMID:33573009	PCS		2/2			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0003270	PMID:33573009	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0011463	PMID:33879678;PMID:8298639	PCS		5/29			C	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0011462	PMID:8298639	PCS		5/15			C	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0003109	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0006554	PMID:29914392	PCS		1/3			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000751	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0007327	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0000952	PMID:29914392;PMID:31426520;PMID:33573009	PCS		4/5			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2024-03-16]
OMIM:277900	Wilson disease		HP:0001402	OMIM:277900	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:277900	Wilson disease		HP:0002311	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0010838	PMID:29914392;PMID:35169583;PMID:31426520	PCS		4/4			P	HPO:probinson[2022-04-28];HPO:skoehler[2012-10-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0031956	PMID:33265091;PMID:29914392;PMID:33879678;PMID:32532881;PMID:33573009	PCS		17/18			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0010837	PMID:33265091;PMID:29914392;PMID:35169583;PMID:34345444;PMID:33879678;PMID:32532881;PMID:33573009	PCS		12/12			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001541	PMID:33573009	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001382	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0001260	PMID:33879678	PCS	HP:0003621	1/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:6000642	PMID:25609909	PCS					P	HPO:probinson[2024-04-03]
OMIM:277900	Wilson disease		HP:0010839	PMID:29914392;PMID:35169583;PMID:33573009	PCS		5/5			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002150	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0000093	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0002071	PMID:34345444	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0006580	PMID:35169583	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000969	PMID:29914392	PCS		3/3			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000726	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0002904	PMID:35169583;PMID:33573009	PCS		2/2			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0032254	PMID:32532881	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002749	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0004409	PMID:31426520	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000007	PMID:8298639	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002548	PMID:31426520	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002307	PMID:33879678	PCS	HP:0003621	1/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000124	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0200032	PMID:33265091;PMID:29914392;PMID:35169583;PMID:34345444;PMID:33879678;PMID:32532881;PMID:33573009	PCS		9/17			P	HPO:probinson[2022-04-28];HPO:skoehler[2010-06-24];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000762	PMID:33265091	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001337	PMID:33265091;PMID:35169583;PMID:31426520	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001259	OMIM:277900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277900	Wilson disease		HP:0001397	PMID:32532881	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0033748	PMID:29914392	PCS		1/3			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001399	PMID:29914392;PMID:33573009	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001271	OMIM:277900	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:277900	Wilson disease		HP:0002240	PMID:35169583;PMID:32532881	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001394	PMID:32532881;PMID:33573009	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0010741	PMID:35169583;PMID:33573009	PCS		2/2			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0003690	PMID:33265091	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002040	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0031964	PMID:33265091;PMID:29914392;PMID:33879678;PMID:32532881;PMID:33573009	PCS		16/18			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000939	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0100785	PMID:29914392	PCS		1/3			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0001903	PMID:33573009	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000934	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0002758	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0025710	PMID:31426520	PCS		1/1			C	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0200122	OMIM:277900	TAS					P	HPO:skoehler[2013-06-11]
OMIM:277900	Wilson disease		HP:0001744	PMID:32532881	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0003621	PMID:34345444;PMID:33879678;PMID:8298639	PCS		20/30			C	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002378	PMID:34345444	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002015	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0002375	PMID:31426520	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002013	PMID:29914392	PCS		1/3			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0002451	PMID:31426520	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0033834	PMID:34345444	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0025709	PMID:33265091;PMID:35169583	PCS		2/2			C	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000829	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0034254	PMID:35169583	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:277900	Wilson disease		HP:0001878	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:277900	Wilson disease		HP:0001873	PMID:31426520;PMID:33573009	PCS		1/2			P	HPO:probinson[2022-04-28];HPO:probinson[2024-03-09];HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0003537	PMID:33573009	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:277900	Wilson disease		HP:0000787	OMIM:277900	IEA					P	HPO:iea[2009-02-17]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0002069	PMID:15115830	PCS		1/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0002521	PMID:15115830	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0001993	PMID:15115830	PCS					P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0030795	PMID:15115830	PCS					P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0005487	PMID:15115830	PCS		1/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0001371	PMID:15115830	PCS		3/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0001263	PMID:15115830	PCS		4/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0032794	PMID:15115830	PCS		1/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0003074	PMID:15115830	PCS	HP:0003623				P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0100651	PMID:15115830	PCS	HP:0003623				P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0007334	PMID:15115830	PCS		1/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0002714	PMID:15115830	PCS		3/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0001488	PMID:15115830	PCS		3/13			P	HPO:probinson[2020-09-02]
OMIM:618856	Diabetes, permanent neonatal 2, with or without neurologic features		HP:0000006	PMID:15115830	PCS					I	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:620311	Premature ovarian failure 21		HP:0000869	PMID:36856110;PMID:35801529	PCS		10/15	FEMALE		P	HPO:probinson[2023-07-09]
OMIM:620311	Premature ovarian failure 21		HP:0011462	PMID:36856110;PMID:35801529	PCS		15/15	FEMALE		C	HPO:probinson[2023-07-09]
OMIM:620311	Premature ovarian failure 21		HP:0008232	PMID:36856110	PCS		11/11	FEMALE		P	HPO:probinson[2023-07-09]
OMIM:620311	Premature ovarian failure 21		HP:0010465	PMID:35801529	PCS		1/4	FEMALE		P	HPO:probinson[2023-07-09]
OMIM:620311	Premature ovarian failure 21		HP:0010464	PMID:35801529	PCS		3/4	FEMALE		P	HPO:probinson[2023-07-09]
OMIM:620311	Premature ovarian failure 21		HP:0008214	PMID:36856110	PCS		11/11	FEMALE		P	HPO:probinson[2023-07-09]
OMIM:620311	Premature ovarian failure 21		HP:0000006	PMID:30924587	PCS					I	HPO:probinson[2023-07-09]
OMIM:620311	Premature ovarian failure 21		HP:0000786	PMID:36856110;PMID:30924587;PMID:35801529	PCS		7/17	FEMALE		P	HPO:probinson[2023-07-09]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0004325	PMID:31564433	PCS		3/5			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000252	PMID:31564433	PCS		7/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0012809	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000750	PMID:31564433	PCS		6/6			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000343	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000486	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0001684	PMID:31564433	PCS	HP:0003577	1/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0001250	PMID:31564433	PCS		1/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0001290	PMID:31564433	PCS		1/5		HP:0012825	P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0012811	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0011833	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0012810	PMID:31564433	PCS		1/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000718	PMID:31564433	PCS		4/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000729	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000448	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000007	PMID:31564433	PCS					I	HPO:probinson[2020-06-25];HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000219	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000455	PMID:31564433	PCS		2/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000400	PMID:31564433	PCS		3/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0007018	PMID:31564433	PCS		3/7			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0001257	PMID:31564433	PCS		2/5			P	HPO:probinson[2020-06-25]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000369	PMID:31564433	PCS		2/7			P	HPO:probinson[2023-02-06]
OMIM:618665	Intellectual developmental disorder, autosomal recessive 72		HP:0000358	PMID:31564433	PCS		2/7			P	HPO:probinson[2023-02-06]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0002069	PMID:12243921	PCS		13/13			P	HPO:probinson[2023-02-19]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0002384	OMIM:607745	IEA		3/13			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0002372	PMID:12243921	PCS		6/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0003593	PMID:12243921	PCS		10/10			C	HPO:probinson[2023-02-19]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0007334	OMIM:607745	IEA					P	HPO:iea[2009-02-17]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0012759	PMID:12243921	PCS		0/13			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-19]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0000961	OMIM:607745	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0000006	PMID:12243921	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607745	Seizures, benign familial infantile, 3		HP:0002104	OMIM:607745	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0003577	PMID:26755636	PCS		5/5			C	HPO:probinson[2022-08-20]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0000407	PMID:26755636	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-20]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0001839	PMID:26755636	PCS		4/5			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0004692	PMID:26755636	PCS		1/5			P	HPO:probinson[2022-08-20]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0000007	PMID:26755636	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-20]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0001171	PMID:26755636	PCS		5/5			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0006159	PMID:26755636	PCS					P	HPO:probinson[2022-08-20]
OMIM:616890	Split-Foot malformation with mesoaxial polydactyly		HP:0010711	PMID:26755636	PCS		1/5			P	HPO:probinson[2022-08-20]
OMIM:616648	Optic atrophy 8		HP:0000572	OMIM:616648	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616648	Optic atrophy 8		HP:0030455	PMID:21349918	PCS					P	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0006958	PMID:21349918	IEA		3/5			P	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0000407	PMID:21349918	PCS					P	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0000648	PMID:21349918	PCS					P	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0000505	PMID:21349918	PCS					P	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0000603	PMID:21349918	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0007104	PMID:21349918	PCS					P	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0001653	OMIM:616648	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616648	Optic atrophy 8		HP:0000006	PMID:21349918	PCS					I	HPO:probinson[2017-06-17]
OMIM:616648	Optic atrophy 8		HP:0001634	PMID:21349918	PCS		3/5			P	HPO:probinson[2017-06-17]
OMIM:231000	Gaucher disease, type III		HP:0002344	OMIM:231000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:231000	Gaucher disease, type III		HP:0004325	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0000486	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0002123	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0002167	OMIM:231000	TAS					P	HPO:probinson[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0004322	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0007817	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0003581	PMID:33483255	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:231000	Gaucher disease, type III		HP:0001251	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0002240	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0001270	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0000716	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0000726	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0011463	PMID:33483255	PCS					C	HPO:probinson[2022-04-05]
OMIM:231000	Gaucher disease, type III		HP:0000007	OMIM:231000	IEA					I	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0004934	OMIM:231000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:231000	Gaucher disease, type III		HP:0001873	OMIM:231000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231000	Gaucher disease, type III		HP:0001744	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0001876	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0002313	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0001336	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:231000	Gaucher disease, type III		HP:0003656	OMIM:231000	IEA					P	HPO:iea[2009-02-17]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0003577	PMID:21109224	PCS		6/6			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0001321	PMID:21109224	PCS		1/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0001250	PMID:21109224	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0000086	PMID:21109224	PCS		2/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0001263	PMID:21109224	PCS				HP:0012829	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0002240	PMID:21109224	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0005484	PMID:21109224	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0000518	PMID:21109224	PCS	HP:0003577	6/6			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0001629	PMID:21109224	PCS		1/6			P	HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0000800	PMID:21109224	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0000007	PMID:21109224	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0000568	PMID:21109224	PCS		1/6			P	HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0002119	PMID:21109224	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0000543	PMID:21109224	PCS		1/6			P	HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0003811	PMID:21109224	PCS		2/6			C	HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0001522	PMID:21109224	PCS		1/6			C	HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0001257	PMID:21109224	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0000028	PMID:21109224	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts		HP:0001347	PMID:21109224	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000365	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0001252	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0001251	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0002240	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000580	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0003593	PMID:1531167	PCS		2/2			C	HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0100651	PMID:1531167	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000939	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0001508	PMID:1531167	PCS		2/2			P	HPO:probinson[2012-03-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000618	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0001944	PMID:1531167	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0001427	PMID:1531167	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000114	PMID:1531167	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000597	PMID:1531167	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0002014	PMID:1531167	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000550	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0002376	PMID:1531167	PCS		1/1			P	HPO:probinson[2012-03-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0002013	PMID:1531167	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0011421	PMID:1531167	PCS		1/2			C	HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0003819	PMID:1531167	PCS		1/2			C	HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000508	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0002748	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0007511	PMID:1531167	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0000103	PMID:1531167	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:560000	Renal tubulopathy, diabetes mellitus, and cerebellar ataxia		HP:0001336	PMID:1531167	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001298	OMIM:614739	TAS					P	HPO:skoehler[2015-01-21]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0002540	OMIM:614739	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0003256	OMIM:614739	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001332	PMID:22683713	PCS		14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001272	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001250	OMIM:614739	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001252	OMIM:614739	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001290	OMIM:614739	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0012444	PMID:22683713	PCS		8/11			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001508	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0002719	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001987	OMIM:614739	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001943	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0002977	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001249	OMIM:614739	TAS		14/14			P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0003128	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0003348	PMID:22683713	PCS		8/13			P	HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0000252	OMIM:614739	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001344	OMIM:614739	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0002376	PMID:22683713	PCS		15/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0011968	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001263	PMID:22683713	PCS		14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0002151	OMIM:614739	TAS		14/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0002071	OMIM:614739	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0040187	OMIM:614739	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0000407	PMID:22683713	PCS		13/14			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0000007	PMID:22683713	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0000648	OMIM:614739	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0001257	PMID:22683713	PCS		13/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:614739	3-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome		HP:0003535	PMID:22683713	PCS		14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:612348	Thrombophilia due to decreased release of tissue plasminogen		HP:0004850	OMIM:612348	TAS					P	HPO:probinson[2013-08-11]
OMIM:612348	Thrombophilia due to decreased release of tissue plasminogen		HP:0000006	OMIM:612348	TAS					I	HPO:probinson[2013-04-06]
OMIM:600994	Deafness, autosomal dominant nonsyndromic sensorineural 5		HP:0000408	OMIM:600994	TAS					P	HPO:skoehler[2010-06-20]
OMIM:600994	Deafness, autosomal dominant nonsyndromic sensorineural 5		HP:0000006	OMIM:600994	TAS					I	HPO:skoehler[2009-02-17]
OMIM:235500	Hemosiderosis, pulmonary, with deficiency of gamma-A globulin		HP:0002086	OMIM:235500	IEA					P	HPO:iea[2009-02-17]
OMIM:235500	Hemosiderosis, pulmonary, with deficiency of gamma-A globulin		HP:0000007	OMIM:235500	IEA					I	HPO:iea[2009-02-17]
OMIM:235500	Hemosiderosis, pulmonary, with deficiency of gamma-A globulin		HP:0002720	OMIM:235500	IEA					P	HPO:iea[2009-02-17]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0001276	PMID:28837161	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0000252	PMID:28837161	PCS		4/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0001344	PMID:28837161	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0011968	PMID:28837161	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0001250	PMID:28837161	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0001263	PMID:28837161	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0001350	PMID:28837161	PCS		2/5			P	HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0003593	PMID:28837161	PCS		5/5			C	HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0001270	PMID:28837161	PCS		5/5			P	HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0012760	PMID:28837161	PCS		5/5			P	HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0000718	PMID:28837161	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0000007	PMID:28837161	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-18]
OMIM:618103	Intellectual developmental disorder, autosomal recessive 64		HP:0001257	PMID:28837161	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:619209	Erythrokeratodermia variabilis et progressiva 7		HP:0002224	PMID:30321533	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619209	Erythrokeratodermia variabilis et progressiva 7		HP:0000970	PMID:30321533	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:619209	Erythrokeratodermia variabilis et progressiva 7		HP:0000007	PMID:30321533	PCS					I	HPO:probinson[2021-03-28];HPO:probinson[2021-03-28]
OMIM:619209	Erythrokeratodermia variabilis et progressiva 7		HP:0000972	PMID:30321533;PMID:31898316	PCS		4/4			P	HPO:probinson[2021-03-28];HPO:probinson[2021-03-28];HPO:probinson[2021-03-28]
OMIM:619209	Erythrokeratodermia variabilis et progressiva 7		HP:0001810	PMID:30321533	PCS		1/1			P	HPO:probinson[2021-03-28]
OMIM:106600	Tooth agenesis, selective, 1		HP:0011463	PMID:8696335	PCS					C	HPO:probinson[2022-08-17]
OMIM:106600	Tooth agenesis, selective, 1		HP:0000668	PMID:8696335	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-17]
OMIM:106600	Tooth agenesis, selective, 1		HP:0000006	PMID:8696335	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-17]
OMIM:618117	Ovarian dysgenesis 7		HP:0003621	PMID:29566152	PCS		4/4			C	HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0000013	PMID:29566152	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0002750	PMID:29566152	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0011969	PMID:29566152	PCS		3/4			P	HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0008232	PMID:29566152	PCS		3/4			P	HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0000007	PMID:29566152	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0000823	PMID:29566152	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0008214	PMID:29566152	PCS		3/4			P	HPO:probinson[2023-06-04]
OMIM:618117	Ovarian dysgenesis 7		HP:0000786	PMID:29566152	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-04]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0006988	PMID:22180640	PCS		1/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000286	PMID:22180640	PCS		8/14			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000486	PMID:22180640	PCS		6/14			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0001250	PMID:22180640	PCS		1/25			P	HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0001274	PMID:22180640	PCS		5/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0001252	PMID:22180640	PCS		12/15			P	HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000717	PMID:22180640	PCS		7/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000316	PMID:22180640	PCS		7/17			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000337	PMID:22180640	PCS		10/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0002119	PMID:22180640	PCS		3/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0009623	PMID:22180640	PCS		3/25			P	HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000218	PMID:22180640	PCS		7/10			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0008734	PMID:22180640	PCS		2/15			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000054	PMID:22180640	PCS		4/15			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000494	PMID:22180640	PCS		7/13			P	HPO:probinson[2023-04-22];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000750	PMID:22180640	PCS		15/17			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0001263	PMID:22180640	PCS		19/21			P	HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0002808	PMID:22180640	PCS		3/25			P	HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000508	PMID:22180640	PCS		4/11			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000268	PMID:22180640	PCS		2/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000400	PMID:22180640	PCS		5/15			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0001357	PMID:22180640	PCS		2/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0007018	PMID:22180640	PCS		8/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000322	PMID:22180640	PCS		6/6			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000006	PMID:22180640	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000248	PMID:22180640	PCS		3/25			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000028	PMID:22180640	PCS		7/15			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000369	PMID:22180640	PCS		4/15			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000545	PMID:22180640	PCS		4/8			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615433	Chromosome 3q13.31 deletion syndrome		HP:0000049	PMID:22180640	PCS		2/15			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-04-22]
OMIM:615355	Noonan syndrome 8		HP:0000286	PMID:23791108	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0007517	PMID:25124994;PMID:23791108	PCS		10/19			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0002202	PMID:23791108	PCS	HP:0011461	1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0004322	PMID:25124994;PMID:23791108	PCS		8/24			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0004482	PMID:25124994;PMID:23791108	PCS		25/33			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0001508	PMID:23791108	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0001629	PMID:25124994;PMID:23791108	PCS		10/16			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0000316	PMID:23791108	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000953	PMID:25124994;PMID:23791108	PCS		9/21			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0001643	PMID:25124994;PMID:23791108	PCS		4/28			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0001642	PMID:23791108	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000974	PMID:25124994;PMID:23791108	PCS		7/22			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0001249	PMID:25124994	PCS		4/18			P	HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0002212	PMID:25124994;PMID:23791108	PCS		21/35			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0000494	PMID:23791108	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0001561	PMID:23791108	PCS	HP:0011461	2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0001520	PMID:23791108	PCS	HP:0003577	3/5			P	HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0011968	PMID:23791108	PCS		2/4			P	HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000470	PMID:23791108	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0001639	PMID:23791108	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000508	PMID:23791108	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000766	PMID:25124994	PCS		5/19			P	HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0000964	PMID:23791108	PCS		1/5			P	HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0001712	PMID:25124994	PCS		14/23			P	HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0001631	PMID:25124994;PMID:23791108	PCS		11/16			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0001653	PMID:23791108	PCS		2/6			P	HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000465	PMID:25124994;PMID:23791108	PCS		17/25			P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0000006	PMID:23791108	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000028	PMID:25124994;PMID:23791108	PCS		10/15	MALE		P	HPO:probinson[2021-05-22];HPO:probinson[2017-05-31]
OMIM:615355	Noonan syndrome 8		HP:0000369	PMID:23791108	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:615355	Noonan syndrome 8		HP:0000962	PMID:23791108	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-22]
OMIM:186000	Synpolydactyly 1		HP:0011939	PMID:9758628	PCS		5/20			P	HPO:probinson[2024-07-22]
OMIM:186000	Synpolydactyly 1		HP:0003577	PMID:9758628	PCS					C	HPO:probinson[2022-12-02]
OMIM:186000	Synpolydactyly 1		HP:0004220	OMIM:186000	IEA					P	HPO:iea[2009-02-17]
OMIM:186000	Synpolydactyly 1		HP:0004692	PMID:9758628	PCS		8/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:186000	Synpolydactyly 1		HP:0008083	OMIM:186000	IEA					P	HPO:iea[2009-02-17]
OMIM:186000	Synpolydactyly 1		HP:0009185	OMIM:186000	IEA					P	HPO:iea[2009-02-17]
OMIM:186000	Synpolydactyly 1		HP:0010055	PMID:9758628	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-02]
OMIM:186000	Synpolydactyly 1		HP:0006042	OMIM:186000	IEA					P	HPO:iea[2009-02-17]
OMIM:186000	Synpolydactyly 1		HP:0006101	OMIM:186000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:186000	Synpolydactyly 1		HP:0004209	OMIM:186000	TAS					P	HPO:probinson[2012-06-04]
OMIM:186000	Synpolydactyly 1		HP:0006159	OMIM:186000	TAS					P	HPO:probinson[2012-06-04]
OMIM:186000	Synpolydactyly 1		HP:0001830	OMIM:186000	IEA					P	HPO:iea[2009-02-17]
OMIM:186000	Synpolydactyly 1		HP:0001841	OMIM:186000	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:186000	Synpolydactyly 1		HP:0000006	PMID:9758628	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-02]
OMIM:186000	Synpolydactyly 1		HP:0001501	OMIM:186000	TAS					P	HPO:iea[2009-02-17]
OMIM:602629	Dystonia 6, torsion		HP:0000473	PMID:19182804	PCS		17/29			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0002356	OMIM:602629	IEA					P	HPO:skoehler[2010-06-18]
OMIM:602629	Dystonia 6, torsion		HP:0003621	PMID:19182804	PCS		16/28			C	HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0001260	OMIM:602629	IEA					P	HPO:skoehler[2010-06-18]
OMIM:602629	Dystonia 6, torsion		HP:0002451	PMID:19182804	PCS		28/29			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0012048	PMID:19182804	PCS		14/29			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0012049	PMID:19182804	PCS		11/29			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0031008	PMID:19182804	PCS		11/29			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0001618	OMIM:602629	IEA					P	HPO:skoehler[2010-06-18]
OMIM:602629	Dystonia 6, torsion		HP:0011462	PMID:19182804	PCS		12/28			C	HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0003829	OMIM:602629	TAS					I	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0000006	PMID:19182804	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0001304	PMID:19182804	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:602629	Dystonia 6, torsion		HP:0001336	OMIM:602629	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0000473	PMID:16685654	PCS		1/1			P	HPO:probinson[2013-06-02]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0003621	PMID:16685654	PCS		1/1			C	HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0000365	PMID:16685654	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0003431	PMID:16685654	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0001332	PMID:16685654	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0002352	PMID:16685654	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0002495	PMID:16685654	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0034721	PMID:16685654	PCS		1/1			P	HPO:probinson[2023-06-05]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0002080	PMID:16685654	PCS		1/1			P	HPO:probinson[2013-06-02]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0000815	PMID:16685654	PCS		1/1			P	HPO:probinson[2013-06-02]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0012692	PMID:16685654	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0009830	PMID:16685654	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0000514	PMID:16685654	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0000007	PMID:16685654	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-21]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0004409	PMID:16685654	PCS		1/1			P	HPO:probinson[2013-06-02]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0002346	PMID:16685654	PCS		1/1			P	HPO:probinson[2013-06-02]
OMIM:613724	Leukoencephalopathy with dystonia and motor neuropathy		HP:0000027	PMID:16685654	PCS		1/1			P	HPO:probinson[2013-06-02]
OMIM:102300	Restless legs syndrome, susceptibility to, 1		HP:0003401	OMIM:102300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:102300	Restless legs syndrome, susceptibility to, 1		HP:0012452	OMIM:102300	TAS					P	HPO:skoehler[2013-11-24]
OMIM:102300	Restless legs syndrome, susceptibility to, 1		HP:0100785	OMIM:102300	TAS					P	HPO:skoehler[2014-06-24]
OMIM:102300	Restless legs syndrome, susceptibility to, 1		HP:0008991	OMIM:102300	TAS					P	HPO:iea[2009-02-17]
OMIM:102300	Restless legs syndrome, susceptibility to, 1		HP:0000006	OMIM:102300	TAS					I	HPO:iea[2009-02-17]
OMIM:102300	Restless legs syndrome, susceptibility to, 1		HP:0001336	OMIM:102300	TAS					P	HPO:iea[2009-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0003577	PMID:28250456	PCS		2/4			C	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0002650	PMID:28250456	PCS		3/4		HP:0003676	P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0000750	PMID:28250456	PCS		3/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0030301	PMID:28250456	PCS		3/3			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0007817	PMID:28250456	PCS		3/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001250	PMID:28250456	PCS		1/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001274	PMID:28250456	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001263	PMID:28250456	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001252	PMID:28250456	PCS		2/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0003593	PMID:28250456	PCS		1/4			C	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0010664	PMID:28250456	PCS		2/3			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0033646	PMID:28250456	PCS		3/3			P	HPO:probinson[2021-04-16]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0033645	PMID:28250456	PCS		3/3			P	HPO:probinson[2021-04-16]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0032327	PMID:28250456	PCS		2/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0012110	PMID:28250456	PCS		3/3			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0011461	PMID:28250456	PCS		1/4			C	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0000007	PMID:28250456	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0000238	PMID:28250456	PCS		1/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0002317	PMID:28250456	PCS		1/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001335	PMID:28250456	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001269	PMID:28250456	PCS		1/4			P	HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001249	PMID:28250456	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-17]
OMIM:617542	Gaze palsy, familial horizontal, with progressive scoliosis, 2		HP:0001347	PMID:28250456	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-17]
OMIM:614063	N-acetylaspartate deficiency		HP:0004325	OMIM:614063	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614063	N-acetylaspartate deficiency		HP:0002136	PMID:19807691	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:614063	N-acetylaspartate deficiency		HP:0000252	OMIM:614063	TAS					P	HPO:probinson[2013-08-10]
OMIM:614063	N-acetylaspartate deficiency		HP:0002078	PMID:19807691	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:614063	N-acetylaspartate deficiency		HP:0000023	OMIM:614063	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614063	N-acetylaspartate deficiency		HP:0004322	OMIM:614063	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614063	N-acetylaspartate deficiency		HP:0001250	PMID:19807691	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:614063	N-acetylaspartate deficiency		HP:0001263	PMID:19807691	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:614063	N-acetylaspartate deficiency		HP:0012708	PMID:19807691	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:614063	N-acetylaspartate deficiency		HP:0005484	PMID:19807691	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:614063	N-acetylaspartate deficiency		HP:0001290	OMIM:614063	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614063	N-acetylaspartate deficiency		HP:0011463	PMID:19807691	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:614063	N-acetylaspartate deficiency		HP:0000007	PMID:19807691	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-02-19]
OMIM:614063	N-acetylaspartate deficiency		HP:0000733	OMIM:614063	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614063	N-acetylaspartate deficiency		HP:0000736	OMIM:614063	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614063	N-acetylaspartate deficiency		HP:0002317	OMIM:614063	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614063	N-acetylaspartate deficiency		HP:0025336	PMID:19807691	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:614063	N-acetylaspartate deficiency		HP:0000742	OMIM:614063	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000286	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000483	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0002188	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000365	PMID:30639322	PCS		4/19			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001250	PMID:30639322	PCS		3/18			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0002263	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000160	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001252	PMID:30639322	PCS		10/16			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0003593	PMID:30639322	PCS					C	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0009381	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000319	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0010055	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000718	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000316	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0100807	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001643	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0002019	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001249	PMID:30639322	IEA		19/19			P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000297	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000494	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0002079	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001382	PMID:30639322	PCS		8/18			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001263	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0004691	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0011800	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001182	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0012585	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000729	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000646	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000767	PMID:30639322	PCS		1/17			P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000047	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000006	PMID:30639322	PCS					I	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000369	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000582	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000343	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001156	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001272	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001270	PMID:30639322	PCS		12/16			P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0008872	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001822	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0002119	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0009765	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0009921	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0009904	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000154	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0002059	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000076	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000431	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0002650	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000750	PMID:30639322	PCS		15/17			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0032388	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0010579	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000508	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000426	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001510	PMID:30639322	PCS		10/16			P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0007018	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000501	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000028	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000589	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0000347	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:618659	Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies		HP:0001831	PMID:30639322	PCS					P	HPO:probinson[2020-07-14]
OMIM:610205	Alagille syndrome 2		HP:0001396	OMIM:610205	TAS					P	HPO:probinson[2013-04-01]
OMIM:610205	Alagille syndrome 2		HP:0003189	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0000089	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0000083	PMID:16773578	PCS					P	HPO:probinson[2013-04-01]
OMIM:610205	Alagille syndrome 2		HP:0000790	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0000093	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0001947	OMIM:610205	TAS					P	HPO:probinson[2013-04-01]
OMIM:610205	Alagille syndrome 2		HP:0000627	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0001636	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0000822	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0000107	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0000337	PMID:16773578	PCS					P	HPO:probinson[2013-04-01]
OMIM:610205	Alagille syndrome 2		HP:0004969	OMIM:610205	TAS					P	HPO:probinson[2013-04-01]
OMIM:610205	Alagille syndrome 2		HP:0000307	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0001631	OMIM:610205	TAS					P	HPO:probinson[2013-04-01]
OMIM:610205	Alagille syndrome 2		HP:0001642	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610205	Alagille syndrome 2		HP:0000006	OMIM:610205	TAS					I	HPO:probinson[2013-01-09]
OMIM:610205	Alagille syndrome 2		HP:0000325	PMID:16773578	PCS					P	HPO:probinson[2013-04-01]
OMIM:610205	Alagille syndrome 2		HP:0002611	OMIM:610205	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107250	Anterior segment dysgenesis 1		HP:0007759	OMIM:107250	TAS					P	HPO:iea[2009-02-17]
OMIM:107250	Anterior segment dysgenesis 1		HP:0007906	OMIM:107250	IEA					P	HPO:skoehler[2018-10-08]
OMIM:107250	Anterior segment dysgenesis 1		HP:0000482	OMIM:107250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107250	Anterior segment dysgenesis 1		HP:0000659	OMIM:107250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107250	Anterior segment dysgenesis 1		HP:0001115	PMID:15286169;PMID:16636655;PMID:18989383	PCS		98/98			P	HPO:iea[2010-12-12]
OMIM:107250	Anterior segment dysgenesis 1		HP:0007700	PMID:15286169;PMID:18989383	PCS		12/60			P	HPO:iea[2010-12-12]
OMIM:107250	Anterior segment dysgenesis 1		HP:0000006	OMIM:107250	TAS					I	HPO:iea[2009-02-17]
OMIM:618881	Galactosemia IV		HP:0012024	PMID:30451973	PCS	HP:0003623	8/8			P	HPO:probinson[2020-06-14]
OMIM:618881	Galactosemia IV		HP:0000518	PMID:30451973	PCS		2/8			P	HPO:probinson[2020-06-14]
OMIM:618881	Galactosemia IV		HP:0001263	PMID:30451973	PCS		0/8			P	HPO:probinson[2020-06-14];HPO:probinson[2024-03-16]
OMIM:618881	Galactosemia IV		HP:0002240	PMID:30451973	PCS		0/8			P	HPO:probinson[2020-06-14];HPO:probinson[2024-03-16]
OMIM:618881	Galactosemia IV		HP:0000007	PMID:30451973	PCS					I	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618881	Galactosemia IV		HP:0006579	PMID:30451973	PCS	HP:0003623	1/8			P	HPO:probinson[2020-06-14]
OMIM:618881	Galactosemia IV		HP:0003623	PMID:30451973	PCS		8/8			C	HPO:probinson[2024-03-16]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0006846	PMID:32160317	PCS		3/3		HP:0025215	P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0003236	PMID:32160317	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0002076	PMID:32160317	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0032792	PMID:32160317	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0012707	PMID:32160317	PCS		2/2			P	HPO:probinson[2021-05-30]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0000007	PMID:32160317	PCS					I	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0003128	PMID:32160317	PCS		3/3			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619221	Sulfide:quinone oxidoreductase deficiency		HP:0001259	PMID:32160317	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:247800	Lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmunehemolytic anemia, and glomerulonephritis		HP:0000099	OMIM:247800	IEA					P	HPO:iea[2009-02-17]
OMIM:247800	Lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmunehemolytic anemia, and glomerulonephritis		HP:0001890	OMIM:247800	IEA					P	HPO:iea[2009-02-17]
OMIM:247800	Lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmunehemolytic anemia, and glomerulonephritis		HP:0000007	OMIM:247800	IEA					I	HPO:iea[2009-02-17]
OMIM:247800	Lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmunehemolytic anemia, and glomerulonephritis		HP:0001888	OMIM:247800	IEA					P	HPO:iea[2009-02-17]
OMIM:247800	Lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmunehemolytic anemia, and glomerulonephritis		HP:0030150	OMIM:247800	TAS					P	HPO:skoehler[2014-11-26]
OMIM:247800	Lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmunehemolytic anemia, and glomerulonephritis		HP:0002090	OMIM:247800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:247800	Lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmunehemolytic anemia, and glomerulonephritis		HP:0010702	OMIM:247800	IEA					P	HPO:iea[2009-02-17]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:6000132	PMID:2294991;PMID:12663448	PCS		3/3			P	HPO:probinson[2024-01-13];HPO:probinson[2024-02-04]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:0006904	OMIM:230450	IEA					P	HPO:iea[2009-02-17]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:0003198	PMID:2294991	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-04]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:0001271	PMID:2294991	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-04]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:0001878	PMID:2294991	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-04]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:0000007	PMID:2294991	PCS		1/1			I	HPO:iea[2009-02-17];HPO:probinson[2024-02-04]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:0001923	PMID:2294991	PCS		1/1			P	HPO:probinson[2024-02-04]
OMIM:230450	Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency		HP:0025435	PMID:2294991	PCS		1/1			P	HPO:probinson[2024-02-04]
OMIM:230450	Gamma-Glutamylcysteine synthetase deficiency, hemolytic anemia dueto		HP:6000834	PMID:17397529	PCS					P	HPO:probinson[2024-08-03]
OMIM:616106	Psoriasis 15, pustular, susceptibility to		HP:0008404	OMIM:616106	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616106	Psoriasis 15, pustular, susceptibility to		HP:0003765	OMIM:616106	IEA					P	HPO:skoehler[2015-01-27]
OMIM:616106	Psoriasis 15, pustular, susceptibility to		HP:0000006	PMID:24791904	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-28]
OMIM:600002	Eiken syndrome		HP:0002663	OMIM:600002	TAS					P	HPO:probinson[2012-07-28]
OMIM:600002	Eiken syndrome		HP:0004325	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0003038	OMIM:600002	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600002	Eiken syndrome		HP:0006429	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0002684	PMID:31297790;PMID:29987841	PCS		2/2			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0004322	PMID:31297790	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0003275	OMIM:600002	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600002	Eiken syndrome		HP:0003155	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0001571	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0001270	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0003071	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0011220	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0000316	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0001847	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0030084	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0006335	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0000179	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0000677	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0001249	PMID:29987841	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:600002	Eiken syndrome		HP:0002652	PMID:31297790	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0001783	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0002373	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0011800	PMID:31297790;PMID:29987841	PCS		2/2			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0032524	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0003180	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0009371	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0100512	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0010584	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0006283	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0005819	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0000706	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0008103	PMID:31297790;PMID:29987841	PCS		2/2			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0002308	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0000007	OMIM:600002	TAS					I	HPO:probinson[2009-02-17]
OMIM:600002	Eiken syndrome		HP:0000268	PMID:31297790;PMID:29987841	PCS		2/2			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0000322	PMID:29987841	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0001216	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:600002	Eiken syndrome		HP:0000885	PMID:31297790	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619553	Deafness, autosomal recessive 118, with cochlear aplasia		HP:0003577	PMID:32369452	PCS		3/3			C	HPO:probinson[2021-10-23]
OMIM:619553	Deafness, autosomal recessive 118, with cochlear aplasia		HP:0001751	PMID:32369452	PCS		0/3			P	HPO:probinson[2021-10-23]
OMIM:619553	Deafness, autosomal recessive 118, with cochlear aplasia		HP:0011375	PMID:32369452	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619553	Deafness, autosomal recessive 118, with cochlear aplasia		HP:0000007	PMID:32369452	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619553	Deafness, autosomal recessive 118, with cochlear aplasia		HP:0008527	PMID:32369452	PCS	HP:0003577	3/3			P	HPO:probinson[2021-10-23]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0002069	PMID:23708187	PCS		5/6			P	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0002133	PMID:23708187	PCS		2/6			P	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0002376	PMID:23708187	PCS		6/6			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0002123	PMID:23708187	PCS		6/6			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0002373	PMID:23708187	PCS		1/6			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0010819	PMID:23708187	PCS		3/6			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0002121	PMID:23708187	PCS		1/6			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0001263	PMID:23708187	PCS		6/6			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0003593	PMID:23708187	PCS		3/6			C	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0010841	PMID:23708187	PCS		4/6			P	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0031475	PMID:23708187	PCS		2/6			P	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0012000	PMID:23708187	PCS		4/6			P	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0012001	PMID:23708187	PCS		4/6			P	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0011463	PMID:23708187	PCS		3/6			C	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0000729	PMID:23708187	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0032792	PMID:23708187	PCS		3/6			P	HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0200134	PMID:23708187	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0000006	PMID:23708187	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0001249	PMID:23708187	PCS		6/6			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-06-26]
OMIM:615369	Develomental and epileptic encephalopathy 94		HP:0020216	PMID:23708187	PCS		3/6			P	HPO:probinson[2021-06-26]
OMIM:612406	Dystonia 17, torsion, autosomal recessive		HP:0000473	OMIM:612406	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612406	Dystonia 17, torsion, autosomal recessive		HP:0001618	OMIM:612406	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612406	Dystonia 17, torsion, autosomal recessive		HP:0001260	OMIM:612406	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612406	Dystonia 17, torsion, autosomal recessive		HP:0004373	OMIM:612406	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612406	Dystonia 17, torsion, autosomal recessive		HP:0000007	OMIM:612406	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613718	Deafness, autosomal recessive 74		HP:0003577	PMID:21185009	PCS					C	HPO:probinson[2022-09-24]
OMIM:613718	Deafness, autosomal recessive 74		HP:0000365	PMID:21185009	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-24]
OMIM:613718	Deafness, autosomal recessive 74		HP:0000007	PMID:21185009	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613718	Deafness, autosomal recessive 74		HP:0000510	PMID:21185009	PCS		0/6			P	HPO:probinson[2022-09-24]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0030139	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0003577	PMID:16385460	PCS		7/12			C	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000483	PMID:16385460	PCS		2/6			P	HPO:skoehler[2018-10-08]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0030138	PMID:16385460	PCS		2/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000540	PMID:16385460	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0031729	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0012805	PMID:16385460	PCS					P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0500041	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000639	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0008499	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000635	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0007663	PMID:16385460	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0001107	PMID:16385460	PCS		6/6			P	HPO:probinson[2013-08-10];HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0002218	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000978	PMID:16385460	PCS		2/6			P	HPO:probinson[2013-08-10]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000577	PMID:16385460	PCS		2/6			P	HPO:skoehler[2018-10-08]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000132	PMID:16385460	PCS		2/4	FEMALE		P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0001022	PMID:16385460	PCS		6/6			P	HPO:probinson[2013-08-10];HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0003540	PMID:16385460	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0011003	PMID:16385460	PCS		1/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0012043	PMID:16385460	PCS		5/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0007750	PMID:16385460	PCS		5/6			P	HPO:skoehler[2018-10-08]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000007	PMID:16385460	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000543	OMIM:614077	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000565	PMID:16385460	PCS		1/6			P	HPO:skoehler[2018-10-08]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0007513	PMID:16385460	PCS		4/6			P	HPO:probinson[2023-03-22]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000421	PMID:16385460	PCS		1/6			P	HPO:skoehler[2019-04-18]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000545	OMIM:614077	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000666	OMIM:614077	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614077	Hermansky-Pudlak syndrome 8		HP:0000225	OMIM:614077	IEA					P	HPO:skoehler[2019-04-18]
OMIM:160750	MYOSITIS		HP:0100614	OMIM:160750	TAS					P	HPO:probinson[2012-07-25]
OMIM:160750	MYOSITIS		HP:0003701	OMIM:160750	TAS					P	HPO:probinson[2009-02-17]
OMIM:160750	MYOSITIS		HP:0000006	OMIM:160750	TAS					I	HPO:probinson[2009-02-17]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0002169	OMIM:607584	IEA					P	HPO:iea[2009-02-17]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0003698	OMIM:607584	IEA					P	HPO:iea[2009-02-17]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0003593	OMIM:607584	IEA					C	HPO:iea[2009-02-17]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0000007	OMIM:607584	IEA					I	HPO:iea[2009-02-17]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0030051	OMIM:607584	IEA					P	HPO:iea[2009-02-17]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0001258	OMIM:607584	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0001257	OMIM:607584	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607584	Spastic paraplegia 24, autosomal recessive		HP:0001347	OMIM:607584	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0001265	OMIM:606842	TAS					P	HPO:probinson[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0005986	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0004575	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0001284	OMIM:606842	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0004571	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0002094	OMIM:606842	TAS					P	HPO:probinson[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0003690	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0005185	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0002093	OMIM:606842	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0008483	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0002936	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0001638	OMIM:606842	IEA					P	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0003745	OMIM:606842	IEA					I	HPO:iea[2009-02-17]
OMIM:606842	Cardioneuromyopathy with hyaline masses and nemaline rods		HP:0003798	OMIM:606842	IEA					P	HPO:skoehler[2010-06-20]
OMIM:616489	Silver-Russell syndrome 3		HP:0004325	PMID:26154720	PCS		4/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0003577	PMID:26154720	PCS		4/4			C	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0004322	PMID:26154720	PCS		4/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0000062	PMID:26154720	PCS		1/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0001252	PMID:26154720	PCS		1/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0004482	PMID:26154720	PCS		4/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0001270	OMIM:616489	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0012741	PMID:26154720	PCS		1/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0009760	PMID:26154720	PCS		1/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0011220	OMIM:616489	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0008897	PMID:26154720	PCS		4/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0001643	OMIM:616489	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0000278	PMID:26154720	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0000995	OMIM:616489	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0001562	PMID:26154720	PCS		1/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0002750	OMIM:616489	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0011968	PMID:26154720	PCS		2/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0001263	PMID:26154720	PCS		1/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0000808	PMID:26154720	PCS		1/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0001518	PMID:26154720	PCS		4/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0004209	PMID:26154720	PCS		2/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0001159	OMIM:616489	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616489	Silver-Russell syndrome 3		HP:0200055	PMID:26154720	PCS		1/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0002007	PMID:26154720	PCS		3/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0000325	PMID:26154720	PCS		3/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0000369	PMID:26154720	PCS		2/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0034391	PMID:26154720	PCS		1/4			P	HPO:probinson[2022-12-16]
OMIM:616489	Silver-Russell syndrome 3		HP:0000006	PMID:26154720	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-16]
OMIM:605387	Cataract 31, multiple types		HP:0100018	OMIM:605387	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605387	Cataract 31, multiple types		HP:0010923	OMIM:605387	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605387	Cataract 31, multiple types		HP:0007787	PMID:17701905	PCS					P	HPO:probinson[2013-02-18]
OMIM:605387	Cataract 31, multiple types		HP:0000006	PMID:17701905	PCS					I	HPO:probinson[2013-01-09]
OMIM:257150	Neutrophil actin dysfunction		HP:0001939	OMIM:257150	IEA					P	HPO:iea[2009-02-17]
OMIM:257150	Neutrophil actin dysfunction		HP:0002718	OMIM:257150	IEA					P	HPO:iea[2009-02-17]
OMIM:257150	Neutrophil actin dysfunction		HP:0000007	OMIM:257150	IEA					I	HPO:iea[2009-02-17]
OMIM:606856	Pancreatic cancer, susceptibility to, 1		HP:0006725	PMID:17194196	PCS					P	HPO:probinson[2020-06-28]
OMIM:606856	Pancreatic cancer, susceptibility to, 1		HP:0000006	PMID:17194196	PCS					I	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:617783	Nephrotic syndrome, type 16		HP:0000100	PMID:25961457	PCS	HP:0011463	3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:617783	Nephrotic syndrome, type 16		HP:0011463	PMID:25961457	PCS		3/3			C	HPO:probinson[2022-11-05]
OMIM:617783	Nephrotic syndrome, type 16		HP:0000790	PMID:25961457	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:617783	Nephrotic syndrome, type 16		HP:0000007	PMID:25961457	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-05]
OMIM:617783	Nephrotic syndrome, type 16		HP:0000093	PMID:25961457	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:617783	Nephrotic syndrome, type 16		HP:0012579	PMID:25961457	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:224800	Ectodermal dysplasia and neurosensory deafness		HP:0007529	OMIM:224800	IEA					P	HPO:iea[2009-02-17]
OMIM:224800	Ectodermal dysplasia and neurosensory deafness		HP:0000407	OMIM:224800	IEA					P	HPO:iea[2009-02-17]
OMIM:224800	Ectodermal dysplasia and neurosensory deafness		HP:0009473	OMIM:224800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:224800	Ectodermal dysplasia and neurosensory deafness		HP:0000007	OMIM:224800	IEA					I	HPO:iea[2009-02-17]
OMIM:224800	Ectodermal dysplasia and neurosensory deafness		HP:0002943	OMIM:224800	IEA					P	HPO:iea[2009-02-17]
OMIM:611494	Atrial fibrillation, familial, 5		HP:0005110	PMID:17603472	PCS					P	HPO:probinson[2017-06-21]
OMIM:611494	Atrial fibrillation, familial, 5		HP:0010982	PMID:17603472	PCS					I	HPO:probinson[2017-06-21]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001254	PMID:18054510	PCS		5/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0000750	PMID:18054510	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0002650	PMID:18054510	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001371	OMIM:201470	IEA					P	HPO:iea[2009-02-17]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0003198	PMID:18054510	PCS		4/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001250	PMID:18054510	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0011968	PMID:18054510	PCS		4/10			P	HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001263	PMID:18054510	PCS		8/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001252	PMID:18054510	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0003593	PMID:18054510	PCS		4/10			C	HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001251	PMID:18054510	PCS		1/8			P	HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0010695	PMID:18054510	PCS		1/10			P	HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0030319	PMID:18054510	PCS		3/10			P	HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0000709	PMID:18054510	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001508	OMIM:201470	IEA					P	HPO:skoehler[2010-06-20]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0011463	PMID:18054510	PCS		2/10			C	HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0000007	PMID:18054510	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0007256	PMID:18054510	PCS		3/7			P	HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0001638	PMID:18054510	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0003219	OMIM:201470	IEA					P	HPO:iea[2009-02-17]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0004911	OMIM:201470	IEA					P	HPO:iea[2009-02-17]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0002500	PMID:18054510	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0000544	PMID:18054510	PCS		1/10			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-22]
OMIM:201470	Acyl-Coa dehydrogenase, short-chain, deficiency of		HP:0003623	PMID:18054510	PCS		4/10			C	HPO:skoehler[2013-03-11];HPO:probinson[2022-12-22]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000286	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0009815	PMID:16826533	PCS		HP:0040280			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000046	PMID:3066902	PCS		1/3			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002980	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0001773	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0010769	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0001171	OMIM:276820	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0003070	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-22]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0009380	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0010173	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0001849	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000916	PMID:3066902	PCS		3/5			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002937	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0009104	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0001964	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002990	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0003041	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0008363	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002827	PMID:16826533	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000007	OMIM:276820	IEA					I	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0006585	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000768	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000884	PMID:3066902	PCS		2/3			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002986	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002987	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000047	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002984	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0006502	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000369	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000885	PMID:3066902	PCS		3/5			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0005613	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000189	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0001552	PMID:3066902	PCS		2/3			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0003498	OMIM:276820	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0005474	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0003252	PMID:3066902	PCS		4/5			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000218	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002436	OMIM:276820	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0002557	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0009767	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000377	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000475	PMID:3066902	PCS		3/5			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0009829	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000431	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0008817	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000276	PMID:3066902	PCS		2/3			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0003982	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0004231	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000151	OMIM:276820	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000470	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0400004	OMIM:276820	TAS					P	HPO:skoehler[2014-09-21]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0005914	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-23]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0000028	PMID:3066902	PCS		2/3			P	HPO:iea[2012-04-24]
OMIM:276820	Ulna and fibula, absence of, with severe limb deficiency		HP:0001798	OMIM:276820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249420	Frank-ter Haar syndrome		HP:0005731	OMIM:249420	IEA					P	HPO:iea[2009-02-17]
OMIM:249420	Frank-ter Haar syndrome		HP:0000485	PMID:20137777;PMID:34538861	PCS		16/17			P	HPO:probinson[2021-09-26];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0001252	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000280	PMID:34538861	PCS		1/1			P	HPO:skoehler[2015-10-16];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0001090	PMID:34538861	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0040016	PMID:20137777	PCS		12/15			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000957	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000916	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0011220	PMID:20137777;PMID:34538861	PCS		16/18			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-07-08];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000316	PMID:20137777;PMID:34538861	PCS		16/16			P	HPO:probinson[2021-09-26];HPO:iea[2009-02-17];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000557	PMID:34538861	PCS		1/1			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0001840	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0020206	PMID:15523657	PCS					P	HPO:probinson[2020-03-14]
OMIM:249420	Frank-ter Haar syndrome		HP:0003623	PMID:34538861	PCS		1/1			C	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0004611	OMIM:249420	IEA					P	HPO:iea[2009-02-17]
OMIM:249420	Frank-ter Haar syndrome		HP:0005469	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0002751	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000494	PMID:34538861	PCS		1/1			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0001385	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0002079	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000293	PMID:20137777;PMID:34538861	PCS		17/17			P	HPO:probinson[2021-09-26];HPO:iea[2009-02-17];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0001061	OMIM:249420	IEA					P	HPO:skoehler[2018-10-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0012385	PMID:20137777;PMID:34538861	PCS		10/18			P	HPO:probinson[2021-09-26];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000767	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0000007	PMID:20137777	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000689	OMIM:249420	IEA					P	HPO:iea[2009-02-17]
OMIM:249420	Frank-ter Haar syndrome		HP:0000520	PMID:20137777	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000248	PMID:20137777;PMID:34538861	PCS		14/18			P	HPO:probinson[2021-09-26];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000369	PMID:34538861	PCS		1/1			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0001776	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0001655	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000187	PMID:20137777	PCS		9/13			P	HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0003015	OMIM:249420	IEA					P	HPO:iea[2009-02-17]
OMIM:249420	Frank-ter Haar syndrome		HP:0000463	PMID:20137777;PMID:34538861	PCS		12/16			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-07-08];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000260	PMID:20137777;PMID:34538861	PCS		17/17			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-07-08];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0001270	PMID:20137777	PCS		12/13			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0002280	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000939	OMIM:249420	TAS					P	HPO:skoehler[2015-10-16]
OMIM:249420	Frank-ter Haar syndrome		HP:0001629	PMID:20137777	PCS		6/12			P	HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000938	OMIM:249420	TAS					P	HPO:skoehler[2015-10-16]
OMIM:249420	Frank-ter Haar syndrome		HP:0000219	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000218	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0000455	PMID:34538861	PCS		1/1			P	HPO:skoehler[2015-10-16];HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000411	PMID:20137777	PCS		8/12			P	HPO:skoehler[2015-10-09];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000212	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0005989	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0009803	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0003026	OMIM:249420	TAS					P	HPO:probinson[2012-05-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0000154	PMID:20137777	PCS		16/16			P	HPO:skoehler[2015-10-16];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0004279	PMID:20137777	PCS		11/16			P	HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0001762	PMID:20137777	PCS		7/15			P	HPO:skoehler[2015-10-16];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0001684	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0000270	OMIM:249420	IEA					P	HPO:iea[2009-02-17]
OMIM:249420	Frank-ter Haar syndrome		HP:0001087	PMID:20137777	PCS	HP:0003577	7/16			P	HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0005280	PMID:34538861	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:249420	Frank-ter Haar syndrome		HP:0002808	PMID:20137777	PCS		8/15			P	HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0001719	PMID:20137777	PCS		2/8			P	HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0006487	PMID:20137777	PCS		8/16			P	HPO:probinson[2012-05-08];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0002645	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0001631	PMID:20137777	PCS		1/12			P	HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0001510	OMIM:249420	TAS					P	HPO:skoehler[2015-10-09]
OMIM:249420	Frank-ter Haar syndrome		HP:0000347	PMID:20137777;PMID:34538861	PCS		16/18			P	HPO:probinson[2021-09-26];HPO:iea[2009-02-17];HPO:probinson[2021-07-08]
OMIM:249420	Frank-ter Haar syndrome		HP:0001634	PMID:20137777	PCS		1/12			P	HPO:probinson[2017-05-29];HPO:probinson[2021-07-08]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0002069	PMID:24784135	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000164	PMID:25823418	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0002188	PMID:25823418	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0004322	PMID:26050939	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001250	PMID:25804403	PCS		0/1			P	HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001252	PMID:25823418;PMID:26050939	PCS		2/3			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0003593	PMID:24482476	PCS		1/2			C	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0033128	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000639	PMID:25804403	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0011463	PMID:24482476	PCS		1/2			C	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0025336	PMID:24784135	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001642	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001249	PMID:24482476	PCS		1/2			P	HPO:skoehler[2015-01-19];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000556	PMID:26050939	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0002553	PMID:25823418	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0003202	PMID:24482476	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000252	PMID:24784135;PMID:26050939	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0006934	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001344	PMID:24784135	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0003487	PMID:24482476	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0002079	PMID:25823418	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0011968	PMID:25804403	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000490	PMID:25804403	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001263	PMID:25823418;PMID:24784135;PMID:26050939;PMID:24482476;PMID:25804403	PCS		8/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000294	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0100660	PMID:25823418	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000007	PMID:24482476	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000400	PMID:24784135;PMID:25804403	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001257	PMID:24482476	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001276	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27];HPO:probinson[2021-09-02]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000582	PMID:25804403	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0002121	PMID:24784135	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001274	PMID:24482476	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0002162	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001270	PMID:25823418;PMID:24784135	PCS		3/3			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001508	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0100704	PMID:25823418;PMID:25804403	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0006297	PMID:25804403	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000733	PMID:24784135	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001347	PMID:24482476	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001320	PMID:24482476	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000154	PMID:25823418	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0032989	PMID:26050939	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0008936	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0002059	PMID:24784135	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000395	PMID:25804403	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000750	PMID:25823418	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0031936	PMID:24784135;PMID:24482476;PMID:25804403	PCS		5/5			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001684	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000193	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000470	PMID:25823418	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0005280	PMID:24784135	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0100952	PMID:25823418;PMID:24482476	PCS		2/3			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0011471	PMID:25823418	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0000748	PMID:26050939	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0030691	PMID:25804403	PCS		1/1			P	HPO:probinson[2021-06-27]
OMIM:615802	Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities		HP:0001319	PMID:24784135	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-06-27]
OMIM:256500	Netherton syndrome		HP:0003577	PMID:19683336	PCS		9/9			C	HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0001036	OMIM:256500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:256500	Netherton syndrome		HP:0003212	OMIM:256500	TAS					P	HPO:probinson[2009-02-17]
OMIM:256500	Netherton syndrome		HP:0003193	OMIM:256500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:256500	Netherton syndrome		HP:0045075	OMIM:256500	IEA					P	HPO:probinson[2009-02-17]
OMIM:256500	Netherton syndrome		HP:0032061	OMIM:256500	IEA					P	HPO:skoehler[2019-04-18]
OMIM:256500	Netherton syndrome		HP:0100665	OMIM:256500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256500	Netherton syndrome		HP:0001508	PMID:19683336	PCS		3/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0011100	OMIM:256500	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:256500	Netherton syndrome		HP:0100806	PMID:19683336	PCS		5/9			P	HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0004779	OMIM:256500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:256500	Netherton syndrome		HP:0004315	OMIM:256500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:256500	Netherton syndrome		HP:0004798	PMID:19683336	PCS		6/9			P	HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0002257	PMID:19683336	PCS		6/9			P	HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0001025	OMIM:256500	IEA					P	HPO:probinson[2009-02-17]
OMIM:256500	Netherton syndrome		HP:0002299	OMIM:256500	TAS					P	HPO:probinson[2012-03-01]
OMIM:256500	Netherton syndrome		HP:0002099	OMIM:256500	IEA					P	HPO:probinson[2009-02-17]
OMIM:256500	Netherton syndrome		HP:0001263	OMIM:256500	IEA					P	HPO:probinson[2009-02-17]
OMIM:256500	Netherton syndrome		HP:0001581	PMID:19683336	PCS		9/9			P	HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0011473	OMIM:256500	TAS					P	HPO:probinson[2012-09-18]
OMIM:256500	Netherton syndrome		HP:0500093	PMID:19683336	PCS		7/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0004906	OMIM:256500	IEA		4/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0002209	OMIM:256500	TAS					P	HPO:probinson[2009-02-17]
OMIM:256500	Netherton syndrome		HP:0000007	PMID:10835624	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0000964	PMID:19683336	PCS		8/9			P	HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0001019	OMIM:256500	IEA					P	HPO:probinson[2009-02-17]
OMIM:256500	Netherton syndrome		HP:0007479	PMID:19683336	PCS		9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-07]
OMIM:256500	Netherton syndrome		HP:0002205	PMID:19683336	PCS		8/9			P	HPO:probinson[2023-06-07];HPO:probinson[2023-06-07]
OMIM:618498	Polydactyly, postaxial, type A10		HP:0003577	PMID:30982135	PCS					C	HPO:probinson[2023-06-10]
OMIM:618498	Polydactyly, postaxial, type A10		HP:0005696	PMID:30982135	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618498	Polydactyly, postaxial, type A10		HP:0001162	PMID:30982135	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618498	Polydactyly, postaxial, type A10		HP:0000007	OMIM:618498	IEA					I	HPO:skoehler[2019-09-07]
OMIM:618498	Polydactyly, postaxial, type A10		HP:0001830	PMID:30982135	IEA					P	HPO:nvasilevsky[2019-09-11]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000286	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0003577	PMID:36084634	PCS		4/4			C	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000582	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0001770	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000189	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000486	PMID:36084634	PCS		2/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0002000	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000160	PMID:36084634	PCS		2/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000185	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0002162	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0011235	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000180	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0010055	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000316	PMID:36084634	PCS		2/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000337	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000218	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0008577	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0002714	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000378	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000278	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0001249	PMID:36084634	PCS		0/3			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000456	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000670	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000494	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000431	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0009928	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000750	PMID:36084634	PCS		2/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000199	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000430	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0001162	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000691	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:6000569	PMID:36084634	PCS					P	HPO:probinson[2024-04-03]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0011823	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000191	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0009370	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000668	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000007	PMID:36084634	PCS					I	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000348	PMID:36084634	PCS		2/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0001830	PMID:36084634	PCS		4/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000268	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0002007	PMID:36084634	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:620107	Orofaciodigital syndrome XIX		HP:0000369	PMID:36084634	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:300752	Protoporphyria, erythropoietic, X-linked		HP:0012187	PMID:18760763	PCS					P	HPO:probinson[2013-08-11]
OMIM:300752	Protoporphyria, erythropoietic, X-linked		HP:0001891	OMIM:300752	TAS		HP:0040283			P	HPO:probinson[2013-12-15]
OMIM:300752	Protoporphyria, erythropoietic, X-linked		HP:0000992	PMID:18760763	PCS					P	HPO:probinson[2013-02-17]
OMIM:300752	Protoporphyria, erythropoietic, X-linked		HP:0011463	OMIM:300752	TAS					C	HPO:probinson[2013-12-15]
OMIM:300752	Protoporphyria, erythropoietic, X-linked		HP:0001081	OMIM:300752	TAS		HP:0040283			P	HPO:probinson[2013-12-15]
OMIM:300752	Protoporphyria, erythropoietic, X-linked		HP:0001423	PMID:18760763	PCS					I	HPO:probinson[2013-01-09]
OMIM:300752	Protoporphyria, erythropoietic, X-linked		HP:0002910	OMIM:300752	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0003577	PMID:11810295;PMID:10951251	IEA		2/2			C	HPO:probinson[2022-05-11]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0001597	PMID:11810295	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0003341	PMID:11810295	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0008066	PMID:11810295;PMID:8012393;PMID:10951251	PCS		3/3			P	HPO:probinson[2022-05-11]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0100613	PMID:8012393	PCS		1/1			C	HPO:probinson[2022-05-11]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0000007	PMID:8012393	PCS					I	HPO:probinson[2022-05-11]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0001522	PMID:11810295;PMID:10951251	PCS		2/2			C	HPO:probinson[2022-05-11]
OMIM:619786	Epidermolysis bullosa, junctional 3B, severe		HP:0200097	PMID:10951251	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:617973	Methemoglobinemia, Alpha type		HP:0003577	PMID:33251782	PCS					C	HPO:probinson[2021-02-19]
OMIM:617973	Methemoglobinemia, Alpha type		HP:0012119	PMID:33251782	PCS					P	HPO:probinson[2021-02-19]
OMIM:617973	Methemoglobinemia, Alpha type		HP:0000961	PMID:33251782	PCS					P	HPO:probinson[2021-02-19]
OMIM:617973	Methemoglobinemia, Alpha type		HP:0000006	PMID:33251782	PCS					I	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:178651	Pulmonic stenosis and deafness		HP:0000365	OMIM:178651	IEA					P	HPO:iea[2009-02-17]
OMIM:178651	Pulmonic stenosis and deafness		HP:0001714	OMIM:178651	TAS					P	HPO:skoehler[2009-02-17]
OMIM:178651	Pulmonic stenosis and deafness		HP:0001642	OMIM:178651	TAS					P	HPO:skoehler[2009-02-17]
OMIM:178651	Pulmonic stenosis and deafness		HP:0000006	OMIM:178651	IEA					I	HPO:iea[2009-02-17]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0004322	PMID:34694367	PCS		5/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001250	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001252	PMID:34694367	PCS		5/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000319	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0012471	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000998	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000316	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000879	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0009623	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0008897	PMID:34694367	PCS		5/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001643	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000278	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000358	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001249	PMID:34694367	PCS		5/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001344	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0002079	PMID:34694367	PCS		3/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0011968	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000729	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001338	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000007	PMID:34694367	PCS					I	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0004209	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000325	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000369	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001655	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000341	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0011918	PMID:34694367	PCS		3/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0010747	PMID:34694367	PCS		3/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001274	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001270	PMID:34694367	PCS		3/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001629	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0009487	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000414	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0004935	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000218	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001864	PMID:34694367	PCS		3/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001562	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0003189	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000750	PMID:34694367	PCS		5/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000276	PMID:34694367	PCS		4/5			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0030048	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0005484	PMID:34694367	PCS		4/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0045025	PMID:34694367	PCS		5/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0011229	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000348	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000307	PMID:34694367	PCS		3/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0000664	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0007413	PMID:34694367	PCS		1/5			P	HPO:probinson[2023-02-28]
OMIM:620113	Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities		HP:0001511	PMID:34694367	PCS		2/5			P	HPO:probinson[2023-02-28]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0003577	PMID:28556411	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0001561	PMID:28556411	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0001321	PMID:28556411	PCS		1/5			P	HPO:probinson[2022-10-07];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0001360	PMID:28556411	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0012444	PMID:28556411	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0012642	PMID:28556411	PCS		2/5			P	HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0001999	PMID:28556411	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0000007	PMID:28556411	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0001305	PMID:28556411	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0000238	PMID:28556411	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0002119	PMID:28556411	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0005989	PMID:28556411	PCS		1/5			P	HPO:probinson[2022-10-07]
OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		HP:0002324	PMID:28556411	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:228960	Flaujeac factor deficiency		HP:0000007	OMIM:228960	IEA					I	HPO:iea[2009-02-17]
OMIM:228960	Flaujeac factor deficiency		HP:0005527	OMIM:228960	IEA					P	HPO:iea[2009-02-17]
OMIM:228960	Flaujeac factor deficiency		HP:0003645	OMIM:228960	IEA					P	HPO:iea[2009-02-17]
OMIM:615816	Immunodeficiency 23		HP:0003212	PMID:24698316	PCS		9/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0020072	PMID:24589341	PCS		3/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002043	PMID:24589341	PCS		2/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0003474	OMIM:615816	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615816	Immunodeficiency 23		HP:0003496	PMID:24698316	PCS		3/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001252	PMID:24698316	PCS		3/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001251	PMID:24589341	PCS		7/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001290	OMIM:615816	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615816	Immunodeficiency 23		HP:0003193	PMID:24589341	PCS		5/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0010783	PMID:24589341	PCS		2/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001508	PMID:24698316	PCS		7/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0032163	PMID:24589341	PCS		1/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002616	PMID:24589341	PCS		1/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001888	PMID:24698316	PCS		2/9			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0000218	OMIM:615816	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615816	Immunodeficiency 23		HP:0001249	PMID:24589341;PMID:24698316	PCS		9/15			P	HPO:probinson[2020-08-26];HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0025615	PMID:24698316	PCS		7/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001265	OMIM:615816	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615816	Immunodeficiency 23		HP:0410323	PMID:24589341	PCS		3/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001880	PMID:24698316	PCS		9/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002650	PMID:24589341;PMID:24698316	PCS		5/17			P	HPO:probinson[2020-08-26];HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0000793	PMID:24589341	PCS		2/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001382	PMID:24698316	PCS		3/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002099	PMID:24589341	PCS		2/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002110	PMID:24589341;PMID:24698316	PCS		11/17			P	HPO:probinson[2020-08-26];HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001260	PMID:24589341	PCS		4/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0200029	OMIM:615816	TAS					P	HPO:skoehler[2015-01-28]
OMIM:615816	Immunodeficiency 23		HP:0001263	PMID:24698316	PCS		6/7			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0011400	PMID:24589341	PCS		4/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0032170	PMID:24698316	IEA		1/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0012189	PMID:24589341	PCS		2/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0040148	PMID:24589341	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0000407	PMID:24589341	PCS		4/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002728	PMID:24698316	PCS		4/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0500093	PMID:24589341	PCS		5/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001878	PMID:24589341	PCS		1/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002726	PMID:24698316	PCS		8/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0000007	PMID:24698316	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0000964	PMID:24698316	PCS		7/9			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0007499	PMID:24589341	PCS		5/8			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0000405	OMIM:615816	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615816	Immunodeficiency 23		HP:0002923	PMID:24589341	PCS		5/6			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002205	PMID:24698316	PCS		9/9			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0003237	PMID:24698316	PCS		3/9			P	HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0002721	OMIM:615816	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615816	Immunodeficiency 23		HP:0001875	PMID:24589341	PCS		2/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2020-08-26]
OMIM:615816	Immunodeficiency 23		HP:0001336	PMID:24589341	PCS		4/8			P	HPO:probinson[2020-08-26]
OMIM:165600	Orbital margin, hypoplasia of		HP:0000564	OMIM:165600	IEA					P	HPO:iea[2009-02-17]
OMIM:165600	Orbital margin, hypoplasia of		HP:0000652	OMIM:165600	IEA					P	HPO:iea[2009-02-17]
OMIM:165600	Orbital margin, hypoplasia of		HP:0000006	OMIM:165600	IEA					I	HPO:iea[2009-02-17]
OMIM:165600	Orbital margin, hypoplasia of		HP:0007647	OMIM:165600	IEA					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0000819	OMIM:209010	IEA					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0000112	OMIM:209010	TAS					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0000407	OMIM:209010	IEA					P	HPO:skoehler[2010-06-18]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0001317	OMIM:209010	IEA					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0000007	OMIM:209010	IEA					I	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0001327	OMIM:209010	IEA					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0007201	OMIM:209010	IEA					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0000093	OMIM:209010	IEA					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0001920	OMIM:209010	IEA					P	HPO:iea[2009-02-17]
OMIM:209010	Atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus,photomyoclonus, and degenerative neurologic disease		HP:0001677	OMIM:209010	IEA					P	HPO:skoehler[2010-06-20]
OMIM:128700	Preauricular fistulae, congenital		HP:0004467	OMIM:128700	TAS					P	HPO:probinson[2009-02-17]
OMIM:128700	Preauricular fistulae, congenital		HP:0000006	OMIM:128700	IEA					I	HPO:iea[2009-02-17]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001276	PMID:36917474	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002421	PMID:28051070	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0003577	PMID:36917474;PMID:28051070	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0000486	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001332	PMID:36917474;PMID:28051070	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0004322	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001250	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001272	PMID:36917474;PMID:28051070	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002066	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001252	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0003593	PMID:36917474	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0004482	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0033725	PMID:36917474;PMID:28051070	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0000518	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0000639	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0000737	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0007366	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002119	PMID:36917474;PMID:28051070	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0003429	PMID:36917474	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002415	PMID:36917474;PMID:28051070	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001249	PMID:36917474;PMID:28051070	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002599	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001347	PMID:36917474;PMID:28051070	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002059	PMID:36917474;PMID:28051070	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002650	PMID:36917474	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002078	PMID:36917474;PMID:28051070	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001344	PMID:36917474;PMID:28051070	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002376	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0003487	PMID:28051070	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0031936	PMID:28051070	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001761	PMID:28051070	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0011968	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001382	PMID:28051070	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001263	PMID:36917474;PMID:28051070	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0000605	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001518	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001998	PMID:36917474;PMID:28051070	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0000007	PMID:28051070	PCS					I	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0000648	PMID:36917474;PMID:28051070	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0002505	PMID:28051070	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620675	Leukodystrophy, hypomyelinating, 27		HP:0001257	PMID:36917474;PMID:28051070	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:601650	Paragangliomas 2		HP:0002664	OMIM:601650	TAS					P	HPO:iea[2009-02-17]
OMIM:601650	Paragangliomas 2		HP:0006824	OMIM:601650	TAS					P	HPO:probinson[2016-07-19]
OMIM:601650	Paragangliomas 2		HP:0006715	OMIM:601650	TAS					P	HPO:iea[2009-02-17]
OMIM:601650	Paragangliomas 2		HP:0008629	OMIM:601650	TAS					P	HPO:probinson[2016-07-22]
OMIM:601650	Paragangliomas 2		HP:0003001	OMIM:601650	TAS					P	HPO:iea[2009-02-17]
OMIM:601650	Paragangliomas 2		HP:0003581	OMIM:601650	TAS					C	HPO:iea[2009-02-17]
OMIM:601650	Paragangliomas 2		HP:0001609	OMIM:601650	TAS					P	HPO:probinson[2016-07-25]
OMIM:601650	Paragangliomas 2		HP:0001605	OMIM:601650	TAS					P	HPO:probinson[2009-02-17]
OMIM:601650	Paragangliomas 2		HP:0030074	OMIM:601650	TAS					P	HPO:skoehler[2015-01-20]
OMIM:601650	Paragangliomas 2		HP:0001686	OMIM:601650	TAS					P	HPO:iea[2009-02-17]
OMIM:601650	Paragangliomas 2		HP:0000006	OMIM:601650	TAS					I	HPO:iea[2009-02-17]
OMIM:601650	Paragangliomas 2		HP:0002886	OMIM:601650	TAS					P	HPO:iea[2009-02-17]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0003621	PMID:24388663	PCS		1/13			C	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0003552	PMID:24388663	PCS		5/10			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0002166	PMID:24388663	PCS		2/12			P	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0001761	PMID:24388663	PCS		3/14			P	HPO:skoehler[2014-02-25]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0003487	PMID:24388663	PCS		13/13			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0002395	PMID:24388663	PCS		14/14			P	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0001260	PMID:24388663	PCS		0/14			P	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0002064	PMID:24388663	PCS		14/14			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0001251	PMID:24388663	PCS		0/14			P	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0031993	PMID:24388663	PCS		2/8			P	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0011463	PMID:24388663	PCS		12/13			C	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0002839	OMIM:615625	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0000007	PMID:24388663	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0030051	PMID:24388663	PCS		4/10			P	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0001258	PMID:24388663	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0001257	PMID:24388663	PCS		13/14			P	HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0003677	PMID:24388663	PCS					C	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-02]
OMIM:615625	Spastic paraplegia 72, autosomal recessive		HP:0000006	PMID:24388663	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-02]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0003577	PMID:11545688	PCS					C	HPO:probinson[2022-03-24]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0000002	PMID:11545688	PCS		0/20			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-24]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0000364	PMID:11545688	PCS		1/20			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-24]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0001156	OMIM:186570	TAS					P	HPO:skoehler[2014-11-26]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0003041	OMIM:186579;PMID:11545688	PCS	HP:0011463	HP:0040283			P	HPO:iea[2012-07-31]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0009381	OMIM:186570	TAS					P	HPO:probinson[2012-07-22]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0010034	OMIM:186579;PMID:11545688	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0006152	OMIM:186579;PMID:11545688	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0009466	OMIM:186579;PMID:11545688	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0002967	OMIM:186570	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0008368	OMIM:186579;PMID:11545688	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0006147	OMIM:186570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0030084	OMIM:186570	TAS					P	HPO:skoehler[2014-09-21]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0009702	OMIM:186579;PMID:11545688	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0000006	PMID:11545688	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-24]
OMIM:186570	Tarsal-Carpal coalition syndrome		HP:0001204	OMIM:186579;PMID:11545688	PCS		HP:0040283			P	HPO:iea[2010-01-20]
OMIM:613254	Tuberous sclerosis-2		HP:0009717	PMID:11112665;PMID:29196670	PCS		60/67			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0009716	PMID:11112665;PMID:29196670	PCS		133/143			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0000365	PMID:31317616	PCS		1/1			P	HPO:probinson[2022-09-01]
OMIM:613254	Tuberous sclerosis-2		HP:0009719	PMID:11112665;PMID:29196670;PMID:31317616;PMID:8825048	PCS		131/138			P	HPO:probinson[2020-09-12];HPO:probinson[2022-09-01];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0009718	PMID:11112665	PCS		13/118			P	HPO:probinson[2020-09-12]
OMIM:613254	Tuberous sclerosis-2		HP:0001250	PMID:11112665;PMID:29196670	PCS		129/130			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0003593	PMID:31317616	PCS		1/1			C	HPO:probinson[2022-09-01]
OMIM:613254	Tuberous sclerosis-2		HP:0010762	OMIM:613254	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613254	Tuberous sclerosis-2		HP:0012469	PMID:14985384;PMID:29196670	PCS		43/76			P	ORCID:0000-0002-0736-9199[2024-06-06];HPO:skoehler[2013-11-28];HPO:probinson[2020-09-12]
OMIM:613254	Tuberous sclerosis-2		HP:0000957	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0000717	PMID:14985384;PMID:29196670	PCS		32/75			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0009720	PMID:31317616	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-01]
OMIM:613254	Tuberous sclerosis-2		HP:0001328	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0006772	PMID:29196670;PMID:31317616	PCS		4/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-01];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0009722	PMID:8825048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0009721	PMID:11112665;PMID:29196670;PMID:31317616	PCS		71/138			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12];HPO:probinson[2022-09-01];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0009724	PMID:11112665;PMID:31317616	PCS		27/129			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12];HPO:probinson[2022-09-01]
OMIM:613254	Tuberous sclerosis-2		HP:0002514	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0007206	PMID:22497611	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:613254	Tuberous sclerosis-2		HP:0001249	PMID:11112665;PMID:29196670;PMID:31317616	PCS		72/97			P	HPO:probinson[2022-09-01];ORCID:0000-0002-0736-9199[2024-06-06];HPO:skoehler[2012-11-18];HPO:probinson[2020-09-12]
OMIM:613254	Tuberous sclerosis-2		HP:0009727	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0010615	PMID:11112665;PMID:29196670	PCS		99/128			P	HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0001662	PMID:8825048	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0009729	PMID:11112665;PMID:8825048	PCS		59/119			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0005564	PMID:31317616	PCS		1/1			P	HPO:probinson[2022-09-01]
OMIM:613254	Tuberous sclerosis-2		HP:0005584	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0001482	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0012798	PMID:11112665;PMID:29196670	PCS		4/24			P	HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0011097	OMIM:613254	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613254	Tuberous sclerosis-2		HP:0009592	OMIM:613254	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613254	Tuberous sclerosis-2		HP:0000826	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0009594	PMID:11112665;PMID:29196670	PCS		35/124			P	HPO:probinson[2020-09-12];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0034198	PMID:8825048	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0001716	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0000107	PMID:11112665	PCS		54/122			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12]
OMIM:613254	Tuberous sclerosis-2		HP:0000821	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0000169	PMID:8825048	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-06-06]
OMIM:613254	Tuberous sclerosis-2		HP:0007018	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0002888	OMIM:613254	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613254	Tuberous sclerosis-2		HP:0009734	OMIM:613254	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613254	Tuberous sclerosis-2		HP:0000006	PMID:11112665	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-12]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000340	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0007759	OMIM:251290	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000343	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001410	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000463	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001332	PMID:20727516	PCS		2/5			P	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001250	PMID:20727516	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000083	OMIM:251290	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001252	PMID:20727516	PCS		3/5			P	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0003593	PMID:20727516	PCS		2/4			C	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0002240	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0410030	PMID:20727516	PCS		1/5			P	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000639	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001508	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000518	OMIM:251290	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0002119	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000218	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001302	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001643	PMID:20727516	PCS		2/5			P	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0002910	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0002514	PMID:20727516	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001744	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000952	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0003623	PMID:20727516	IEA		2/4			C	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001347	PMID:20727516	PCS		4/5			P	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0008936	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000252	OMIM:251290	IEA					P	HPO:skoehler[2010-06-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001321	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001263	PMID:20727516	PCS		5/5		HP:0012829	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000308	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001339	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001537	PMID:20727516	PCS		1/5			P	HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000007	PMID:20727516	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000967	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0002922	PMID:20727516	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-20]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001873	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001257	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0002126	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0000369	OMIM:251290	IEA					P	HPO:skoehler[2010-06-19]
OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria		HP:0001655	PMID:20727516	PCS		1/5			P	HPO:probinson[2022-03-20]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0001792	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0003771	OMIM:606895	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0000691	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0004253	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0011835	OMIM:606895	TAS					P	HPO:skoehler[2013-06-05]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0010259	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0001859	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0009882	OMIM:606895	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0005819	OMIM:606895	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0009843	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0000006	OMIM:606895	IEA					I	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0006106	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0009803	OMIM:606895	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0001204	OMIM:606895	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606895	Symphalangism, distal, with microdontia, dental pulp stones, and narrowedzygomatic arch		HP:0001798	OMIM:606895	IEA					P	HPO:iea[2009-02-17]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0003577	PMID:25845469	PCS		2/2			C	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001332	PMID:25845469	PCS		1/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0002187	PMID:30847200;PMID:25845469	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-04];HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0003593	PMID:25845469	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0033725	PMID:25845469	PCS		1/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0012110	PMID:25845469	PCS		2/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001629	PMID:25845469	PCS	HP:0003577	1/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0011463	PMID:30847200	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0000737	PMID:25845469	PCS	HP:0003593	2/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001249	PMID:21868677	PCS		5/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0008936	PMID:25845469	PCS		2/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0000252	PMID:30847200;PMID:21868677	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-06-04];HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001344	PMID:25845469	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0000750	PMID:30847200	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0002353	PMID:25845469	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0002474	PMID:25845469	PCS		2/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001266	PMID:25845469	PCS		1/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001288	PMID:30847200	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0011968	PMID:25845469	PCS	HP:0003593	2/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001263	PMID:30847200;PMID:25845469	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0100021	PMID:30847200;PMID:25845469	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0007030	PMID:25845469	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0000007	PMID:21868677;PMID:25845469	PCS		20/20			I	HPO:probinson[2013-08-10];HPO:probinson[2022-04-04];ORCID:0000-0002-0736-9199[2024-06-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001631	PMID:25845469	PCS	HP:0003577	1/2			P	HPO:probinson[2022-04-04]
OMIM:614249	Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy		HP:0001257	PMID:30847200;PMID:25845469	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-04];HPO:probinson[2022-04-04]
OMIM:165199	Optic atrophy, hearing loss, and peripheral neuropathy, autosomaldominant		HP:0002166	OMIM:165199	IEA					P	HPO:iea[2009-02-17]
OMIM:165199	Optic atrophy, hearing loss, and peripheral neuropathy, autosomaldominant		HP:0000408	OMIM:165199	IEA	HP:0003621				P	HPO:iea[2009-02-17]
OMIM:165199	Optic atrophy, hearing loss, and peripheral neuropathy, autosomaldominant		HP:0000505	OMIM:165199	IEA	HP:0003621				P	HPO:iea[2009-02-17]
OMIM:165199	Optic atrophy, hearing loss, and peripheral neuropathy, autosomaldominant		HP:0000648	OMIM:165199	IEA					P	HPO:iea[2009-02-17]
OMIM:165199	Optic atrophy, hearing loss, and peripheral neuropathy, autosomaldominant		HP:0000006	OMIM:165199	IEA					I	HPO:iea[2009-02-17]
OMIM:165199	Optic atrophy, hearing loss, and peripheral neuropathy, autosomaldominant		HP:0002522	OMIM:165199	IEA					P	HPO:iea[2009-02-17]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002542	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002067	PMID:21278747	PCS		1/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000365	PMID:21278747	PCS		1/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0003596	PMID:21278747	PCS		1/4			C	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001332	PMID:21278747	PCS		2/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002186	OMIM:615157	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002066	PMID:21278747	PCS		3/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002385	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001251	PMID:21278747	PCS		1/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0010521	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002180	OMIM:615157	TAS				HP:0003676	P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000716	OMIM:615157	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000639	PMID:21278747	PCS		2/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0011463	PMID:21278747	PCS		1/4			C	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000718	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0007289	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001324	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002311	PMID:21278747	PCS		1/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0003202	PMID:21278747	PCS		1/4			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000651	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0003487	PMID:21278747	PCS		1/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002871	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0011924	PMID:21278747	PCS		4/4			P	HPO:probinson[2023-03-22];HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001260	PMID:21278747	PCS		3/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001263	OMIM:615157	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002075	OMIM:615157	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002070	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001618	PMID:21278747	PCS		2/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000007	PMID:21278747	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000722	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001337	OMIM:615157	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001259	PMID:21278747	PCS		2/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000764	PMID:21278747	PCS		3/4			P	HPO:probinson[2023-03-22];HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002322	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001310	PMID:21278747	PCS		1/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001272	PMID:21278747	PCS		2/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002120	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0100543	PMID:21278747	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000738	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000739	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002313	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0001347	PMID:21278747	PCS		1/4			P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002059	OMIM:615157	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002015	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0003621	PMID:21278747	PCS		2/4			C	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0002650	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000709	OMIM:615157	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0012760	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0034332	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615157	Mitochondrial complex III deficiency, nuclear type 2		HP:0000745	PMID:21278747	PCS		1/4			P	HPO:probinson[2023-03-22]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0001792	OMIM:615631	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0000980	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0004322	OMIM:615631	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0002240	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0010972	PMID:23716552	PCS		3/3			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-05-28]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0011273	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0012132	OMIM:615631	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0001903	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0034278	PMID:23716552	PCS		3/3			P	HPO:probinson[2022-06-04]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0000007	PMID:23716552	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2022-05-28]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0001923	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0001159	OMIM:615631	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0001510	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0000952	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0001744	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615631	Anemia, congenital dyserythropoietic, type Ib		HP:0004447	OMIM:615631	TAS					P	HPO:skoehler[2014-02-25]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0000253	PMID:27392077	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0001265	PMID:27392077	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0003577	PMID:27392077	PCS		1/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0000486	PMID:27392077	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0002540	PMID:27392077	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0000750	PMID:27392077	PCS		4/4			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0003487	PMID:27392077	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0001321	PMID:27392077	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0002120	PMID:27392077	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0001250	PMID:27392077	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0001263	PMID:27392077	PCS		4/4			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0001252	PMID:27392077	PCS		2/4			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0003593	PMID:27392077	PCS		3/4			C	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0002194	PMID:27392077	PCS		3/4			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0010862	PMID:27392077	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0012510	PMID:27392077	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0033725	PMID:27392077	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0012110	PMID:27392077	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0034353	PMID:27392077	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0000737	PMID:27392077	PCS		2/3			P	HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0000007	PMID:25558065	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0001249	PMID:27392077	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617026	Pontocerebellar hypoplasia, type 2F		HP:0001347	PMID:27392077	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0003496	PMID:12958596	PCS		3/3			P	HPO:probinson[2012-06-08];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0200117	PMID:12958596	PCS		1/3			P	HPO:skoehler[2013-06-10];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0011463	PMID:12958596	PCS		2/2			C	HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0000031	PMID:12958596	PCS		1/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0002959	PMID:12958596	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0002718	PMID:12958596	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0000007	PMID:12958596	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0002716	PMID:12958596	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0002720	PMID:12958596	PCS		3/3			P	HPO:probinson[2012-06-08];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0002721	PMID:12958596	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-08]
OMIM:608106	Immunodeficiency with hyper IgM, type 5		HP:0004315	PMID:12958596	PCS		3/3			P	HPO:probinson[2012-06-08];HPO:probinson[2022-11-08]
OMIM:141749	Fetal hemoglobin quantitative trait locus 1		HP:0011904	OMIM:141749	TAS					P	HPO:probinson[2013-12-15]
OMIM:141749	Fetal hemoglobin quantitative trait locus 1		HP:0000006	OMIM:141749	TAS					I	HPO:probinson[2009-02-17]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000286	PMID:37963460	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0004325	PMID:37963460	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0010804	PMID:37963460	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0002023	PMID:37963460	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000486	PMID:37963460	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0004322	PMID:37963460	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001250	PMID:37963460	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001252	PMID:37963460	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0003593	PMID:37963460	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000319	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000718	PMID:37963460	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0012471	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000316	PMID:37963460	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000678	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000752	PMID:37963460	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001643	PMID:37963460	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0002536	PMID:37963460	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001763	PMID:37963460	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000278	PMID:37963460	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001249	PMID:37963460	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000252	PMID:37963460	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000175	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000494	PMID:37963460	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0006979	PMID:37963460	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001344	PMID:37963460	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0002079	PMID:37963460	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0011968	PMID:37963460	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001263	PMID:37963460	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0031510	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000407	PMID:37963460	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000729	PMID:37963460	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000007	PMID:37963460	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001852	PMID:37963460	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000322	PMID:37963460	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001653	PMID:37963460	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000047	PMID:37963460	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000520	PMID:37963460	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000402	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000369	PMID:37963460	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000126	PMID:37963460	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001776	PMID:37963460	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000341	PMID:37963460	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000582	PMID:37963460	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001274	PMID:37963460	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000262	PMID:37963460	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0011237	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001270	PMID:37963460	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0040080	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001629	PMID:37963460	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0008551	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000733	PMID:37963460	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0006695	PMID:37963460	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0002119	PMID:37963460	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000218	PMID:37963460	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000411	PMID:37963460	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001562	PMID:37963460	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0002213	PMID:37963460	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001561	PMID:37963460	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001363	PMID:37963460	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000750	PMID:37963460	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0005280	PMID:37963460	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001518	PMID:37963460	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000426	PMID:37963460	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0001631	PMID:37963460	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620852	Neurodevelopemental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities		HP:0000028	PMID:37963460	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:609218	Foveal hypoplasia 2		HP:0025551	OMIM:609218	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609218	Foveal hypoplasia 2		HP:0000483	PMID:24045842	PCS		9/9			P	HPO:probinson[2023-03-22]
OMIM:609218	Foveal hypoplasia 2		HP:0000486	PMID:24045842	PCS		6/9			P	HPO:probinson[2023-03-22]
OMIM:609218	Foveal hypoplasia 2		HP:0001492	OMIM:609218	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:609218	Foveal hypoplasia 2		HP:0003593	PMID:24045842	PCS		9/9			C	HPO:probinson[2023-03-22]
OMIM:609218	Foveal hypoplasia 2		HP:0000639	PMID:24045842	PCS	HP:0003593	9/9			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-22]
OMIM:609218	Foveal hypoplasia 2		HP:0000627	OMIM:609218	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:609218	Foveal hypoplasia 2		HP:0008001	OMIM:609218	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609218	Foveal hypoplasia 2		HP:0007750	PMID:24045842	PCS		9/9			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-22]
OMIM:609218	Foveal hypoplasia 2		HP:0000007	PMID:24045842	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-22]
OMIM:609218	Foveal hypoplasia 2		HP:0000568	OMIM:609218	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:609218	Foveal hypoplasia 2		HP:0007663	PMID:24045842	PCS	HP:0003593	9/9			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-22]
OMIM:609218	Foveal hypoplasia 2		HP:0001137	OMIM:609218	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0001055	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0002024	OMIM:214900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0003077	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0003155	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0001394	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0002240	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0002908	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0000007	OMIM:214900	IEA					I	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0006566	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0001004	OMIM:214900	TAS					P	HPO:skoehler[2010-06-18]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0002910	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0000952	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:214900	Cholestasis-Lymphedema syndrome		HP:0001744	OMIM:214900	IEA					P	HPO:iea[2009-02-17]
OMIM:263550	Polymyoclonus, infantile		HP:0007295	OMIM:263550	IEA					P	HPO:iea[2009-02-17]
OMIM:263550	Polymyoclonus, infantile		HP:0000737	OMIM:263550	IEA					P	HPO:iea[2009-02-17]
OMIM:263550	Polymyoclonus, infantile		HP:0001251	OMIM:263550	IEA					P	HPO:iea[2009-02-17]
OMIM:263550	Polymyoclonus, infantile		HP:0000007	OMIM:263550	IEA					I	HPO:iea[2009-02-17]
OMIM:263550	Polymyoclonus, infantile		HP:0001336	OMIM:263550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:615619	CHOLANGIOCARCINOMA		HP:0030153	OMIM:615619	IEA					P	HPO:skoehler[2015-01-27]
OMIM:266400	Reese retinal dysplasia		HP:0007968	OMIM:266400	TAS					P	HPO:probinson[2015-07-19]
OMIM:266400	Reese retinal dysplasia		HP:0000007	OMIM:266400	TAS					I	HPO:iea[2009-02-17]
OMIM:266400	Reese retinal dysplasia		HP:0007973	OMIM:266400	TAS					P	HPO:skoehler[2015-01-27]
OMIM:613268	Corneal dystrophy, Fuchs endothelial, 4		HP:0001131	PMID:18024964	PCS					P	HPO:skoehler[2013-01-09];HP:probinson[2019-02-24]
OMIM:613268	Corneal dystrophy, Fuchs endothelial, 4		HP:0000505	PMID:25007886	PCS	HP:0003584				P	HP:probinson[2019-02-24]
OMIM:613268	Corneal dystrophy, Fuchs endothelial, 4		HP:0012038	PMID:25007886	PCS		4/4			P	HP:probinson[2019-02-24]
OMIM:613268	Corneal dystrophy, Fuchs endothelial, 4		HP:0000006	PMID:18024964	PCS					I	HP:probinson[2019-02-24]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0003642	PMID:22305527	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0000486	PMID:22305527	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0001410	PMID:22305527	PCS		1/1			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0031936	PMID:22305527	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0001252	PMID:22305527	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0001263	PMID:22305527	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0003593	PMID:22305527	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0002020	PMID:22305527	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0001508	PMID:22305527	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0000938	PMID:22305527	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0012450	PMID:22305527	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0000007	PMID:22305527	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0005616	PMID:22305527	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:614507	Congenital disorder of glycosylation, type IR		HP:0410018	PMID:22305527	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-25]
OMIM:619745	Noonan syndrome 14		HP:0000286	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001377	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0004322	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001252	PMID:34626534	PCS		3/4			P	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0003593	PMID:34626534	PCS		1/3			C	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000280	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0045075	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0006191	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000958	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0012471	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000316	PMID:34626534	PCS		3/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001888	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001763	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001642	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000358	PMID:34626534	PCS		4/4			P	HPO:probinson[2023-02-06]
OMIM:619745	Noonan syndrome 14		HP:0000494	PMID:34626534	PCS		3/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001263	PMID:34626534	PCS		3/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0008081	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000767	PMID:34626534	PCS		4/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000007	PMID:34626534	PCS					I	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0002705	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001659	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000768	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0007678	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000325	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000369	PMID:34626534	PCS		4/4			P	HPO:probinson[2023-02-06]
OMIM:619745	Noonan syndrome 14		HP:0000341	PMID:34626534	PCS		4/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0003577	PMID:34626534	PCS		2/3			C	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000343	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0002162	PMID:34626534	PCS		4/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0003691	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0005272	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0008070	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000975	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000978	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0030084	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0002212	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000154	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0006956	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001561	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000470	PMID:34626534	PCS		4/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001639	PMID:34626534	PCS		3/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0002808	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000426	PMID:34626534	PCS		4/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000307	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0002967	PMID:34626534	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000465	PMID:34626534	PCS		4/4			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0000028	PMID:34626534	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:619745	Noonan syndrome 14		HP:0001634	PMID:34626534	PCS		1/4			P	HPO:probinson[2022-04-05]
OMIM:617768	Kleefstra syndrome 2		HP:0025352	PMID:29069077	PCS					I	HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0000252	OMIM:617768	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617768	Kleefstra syndrome 2		HP:0000750	PMID:29069077	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0002650	PMID:29069077	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0000574	OMIM:617768	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617768	Kleefstra syndrome 2		HP:0000232	PMID:29069077;OMIM:617768	IEA		11/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0001250	OMIM:617768	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617768	Kleefstra syndrome 2		HP:0000193	PMID:29069077	PCS		1/6			P	HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0001263	PMID:29069077	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0001252	PMID:29069077	PCS	HP:0011463	3/6			P	HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0001290	OMIM:617768	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617768	Kleefstra syndrome 2		HP:0011800	PMID:29069077	PCS		2/3			P	HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0002808	PMID:29069077	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0000729	PMID:29069077	PCS		3/6			P	HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0001999	OMIM:617768	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617768	Kleefstra syndrome 2		HP:0100716	PMID:29069077	IEA		1/6			P	HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0001357	PMID:29069077	PCS		1/6			P	HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0001510	OMIM:617768	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617768	Kleefstra syndrome 2		HP:0001249	PMID:29069077	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-04-16]
OMIM:617768	Kleefstra syndrome 2		HP:0000006	OMIM:617768	IEA					I	HPO:skoehler[2019-04-18]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0003577	PMID:23542699	PCS		10/10			C	HPO:skoehler[2013-10-06];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000340	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001792	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000365	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001156	OMIM:614261	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0004322	OMIM:614261	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0025104	PMID:23542699	PCS		10/10			P	HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001250	PMID:23542699	PCS	HP:0003593	10/10			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001250	OMIM:614261	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001252	OMIM:614261	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0003196	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0012448	OMIM:614261	TAS					P	HPO:skoehler[2013-11-28]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001290	OMIM:614261	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0010721	OMIM:614261	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0012469	PMID:23542699	PCS		4/9			P	HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001508	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001629	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0009882	OMIM:614261;PMID:23542699	PCS		19/20			P	HPO:probinson[2023-06-08];HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000316	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0030084	OMIM:614261	TAS					P	HPO:skoehler[2014-09-21]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0003429	PMID:23542699	PCS		5/8			P	HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0025517	PMID:23542699	PCS		6/7			P	HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001667	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000253	PMID:23542699	PCS		10/10			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0002059	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000175	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000076	OMIM:614261	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0002079	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001263	PMID:23542699	PCS		10/10			P	HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001285	PMID:23542699	PCS		8/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0011344	OMIM:614261	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0012510	PMID:23542699	PCS		9/9			P	HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001518	PMID:23542699	PCS		7/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000508	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000327	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000007	PMID:23542699	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000648	PMID:23542699	PCS		6/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001631	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000369	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001336	PMID:23542699	PCS		6/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0001655	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0009879	PMID:23542699	PCS		9/9			P	HPO:probinson[2023-06-08]
OMIM:614261	Microcephaly-Capillary malformation syndrome		HP:0000445	OMIM:614261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0002293	OMIM:125595	TAS					P	HPO:probinson[2009-02-17]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0000502	OMIM:125595	IEA					P	HPO:iea[2015-02-01]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0007455	PMID:16960809	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-25]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0007588	PMID:16960809	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-25]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0000966	PMID:16960809	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0000972	PMID:16960809	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-25]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0008404	OMIM:125595	TAS					P	HPO:skoehler[2013-05-03]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0000006	PMID:16960809	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-25]
OMIM:125595	Dermatopathia pigmentosa reticularis		HP:0012788	OMIM:125595	TAS					P	HPO:probinson[2015-02-01]
DECIPHER:17	Sotos syndrome		HP:0000098	DECIPHER:17	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:17	Sotos syndrome		HP:0005616	DECIPHER:17	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:17	Sotos syndrome		HP:0000256	DECIPHER:17	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:17	Sotos syndrome		HP:0001249	DECIPHER:17	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:17	Sotos syndrome		HP:0000303	DECIPHER:17	IEA					P	HPO:skoehler[2013-05-29]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0003026	PMID:31914175	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0002015	PMID:31914175	PCS		1/3			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0002650	PMID:31914175	PCS		1/6		HP:0012828	P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0005521	PMID:31914175	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0005257	PMID:31914175	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0002098	PMID:31914175	PCS		2/3			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0002092	PMID:31914175	PCS		1/3			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0001270	PMID:31914175	PCS		1/3			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0002280	PMID:31914175	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0011421	PMID:31914175	PCS		1/6			C	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0012385	PMID:31914175	PCS		2/6			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0011461	PMID:31914175	PCS		6/6			C	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0003826	PMID:31914175	PCS		1/6			C	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0000007	PMID:31914175	PCS					I	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0001635	PMID:31914175	PCS		1/3			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0000964	PMID:31914175	PCS		1/2			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0006487	PMID:31914175	PCS		5/6			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0001511	PMID:31914175	PCS		3/3			P	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0003811	PMID:31914175	PCS		3/6			C	HPO:probinson[2022-04-19]
OMIM:619751	Stuve-Wiedemann syndrome 2		HP:0001873	PMID:31914175	PCS		1/2			P	HPO:probinson[2022-04-19]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0004325	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002389	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000365	PMID:37075751	PCS		2/2			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0004322	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0008807	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0003196	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0003593	PMID:37075751	PCS		1/17			C	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0012469	PMID:37075751	PCS		1/18			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0034260	PMID:25913037	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000238	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000637	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001605	PMID:37075751	PCS		2/2			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000636	PMID:25913037;PMID:37075751	PCS		2/4			P	HPO:probinson[2022-09-24];ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001601	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0003623	PMID:37075751	PCS		1/17			C	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000494	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000252	PMID:25913037;PMID:37075751	PCS		6/16			P	ORCID:0000-0001-7941-2961[2024-04-01];HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0003764	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000490	PMID:37075751	PCS		2/2			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011800	PMID:25913037	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0034392	PMID:37075751	PCS		2/16			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000403	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0004209	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000400	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001059	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000006	PMID:25913037	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000369	PMID:37075751	PCS		6/17			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002786	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000126	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001336	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0003577	PMID:25913037;PMID:37075751	PCS		15/20			C	HPO:probinson[2022-09-24];ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000582	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011639	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000463	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001270	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0012049	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000337	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001305	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0004937	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002119	PMID:37075751	PCS		1/10			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000218	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0004415	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002410	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002015	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002650	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002376	PMID:37075751	PCS		1/16			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0010819	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0200128	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0012712	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011224	PMID:25913037	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011471	PMID:37075751	PCS		2/2			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000508	PMID:37075751	PCS		5/18			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0200134	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000347	PMID:25913037;PMID:37075751	PCS		9/21			P	ORCID:0000-0001-7941-2961[2024-04-01];HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0004942	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000286	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002980	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001250	PMID:37075751	PCS		5/5			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0003396	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001252	PMID:37075751	PCS		10/17			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002061	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0410030	PMID:37075751	PCS		2/17			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011577	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0040064	PMID:37075751	PCS		6/17			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0034185	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011463	PMID:37075751	PCS		3/17			C	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011342	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001647	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000316	PMID:37075751	PCS		9/16			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000954	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001800	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001643	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000278	PMID:25913037	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001249	PMID:37075751	PCS		0/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000175	PMID:25913037;PMID:37075751	PCS		6/20			P	ORCID:0000-0001-7941-2961[2024-04-01];HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000453	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000574	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001263	PMID:37075751	PCS		8/14			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0410263	PMID:37075751	PCS		5/12			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011443	PMID:37075751	PCS		1/16			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0030307	PMID:25913037	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011569	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0009892	PMID:25913037	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0011330	PMID:37075751	PCS		3/18			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000327	PMID:25913037	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0008689	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000324	PMID:37075751	PCS		3/18			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001655	PMID:37075751	PCS		4/14			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000023	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001508	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001629	PMID:37075751	PCS		3/14			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0008551	PMID:25913037;PMID:37075751	PCS		5/21			P	ORCID:0000-0001-7941-2961[2024-04-01];HPO:skoehler[2015-08-16];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0002835	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0009921	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000652	PMID:25913037	PCS		1/3			P	HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000256	PMID:37075751	PCS		0/13			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001363	PMID:37075751	PCS		0/15			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001362	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0005280	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0009110	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000668	PMID:37075751	PCS		2/7			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0001511	PMID:37075751	PCS		3/14			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0000028	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:616462	Acrofacial dysostosis, Cincinnati type		HP:0004502	PMID:37075751	PCS		1/1			P	ORCID:0000-0001-7941-2961[2024-04-01]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0003676	OMIM:151200	TAS					C	HPO:skoehler[2015-12-30]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0000582	OMIM:151200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001156	OMIM:151200	IEA					P	HPO:iea[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001376	PMID:24442880	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0004322	OMIM:151200	IEA					P	HPO:iea[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0000581	OMIM:151200	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001230	PMID:24442880	PCS		1/7			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0000482	OMIM:151200	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0002020	PMID:24442880	PCS		1/7			P	HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0010049	PMID:24442880	PCS		1/7			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0012745	PMID:24442880	PCS		7/7			P	HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0010743	OMIM:151200	TAS					P	HPO:skoehler[2013-07-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0002816	OMIM:151200	IEA					P	HPO:iea[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001822	OMIM:151200	TAS					P	HPO:probinson[2013-03-11]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001602	OMIM:151200	IEA					P	HPO:iea[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0009803	PMID:24442880	PCS		1/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001220	PMID:24442880	PCS		4/7			P	HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0004279	OMIM:151200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001387	PMID:24442880	PCS		4/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0001761	OMIM:151200	TAS					P	HPO:skoehler[2013-07-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0045025	PMID:24442880	PCS		7/7			P	HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0011304	OMIM:151200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0002829	PMID:24442880	PCS		5/7			P	HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0007311	OMIM:151200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0002967	OMIM:151200	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0006247	OMIM:151200	TAS					P	HPO:skoehler[2013-07-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0009778	OMIM:151200	TAS					P	HPO:skoehler[2013-07-17]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0000006	PMID:24442880	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:151200	Chromosome 8q22.1 duplication syndrome		HP:0004602	PMID:24442880	PCS		2/7			P	HPO:probinson[2022-03-20]
OMIM:255960	Myxoma, intracardiac		HP:0006691	OMIM:255960	TAS					P	HPO:iea[2009-02-17]
OMIM:255960	Myxoma, intracardiac		HP:0011672	OMIM:255960	TAS					P	HPO:probinson[2020-07-19]
OMIM:255960	Myxoma, intracardiac		HP:0006689	OMIM:255960	TAS					P	HPO:iea[2009-02-17]
OMIM:255960	Myxoma, intracardiac		HP:0000006	OMIM:255960	TAS					I	HPO:skoehler[2017-07-13]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000154	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0030799	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000286	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000252	PMID:35196516	PCS		4/10			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000494	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000750	PMID:35196516	PCS		10/10			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000365	PMID:35196516	PCS		6/8			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0004322	PMID:35196516	PCS		3/10			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0002373	PMID:35196516	PCS		6/11			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0002000	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0001263	PMID:35196516	PCS		12/12			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0001274	PMID:35196516	PCS		1/7			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0003593	PMID:35196516	PCS					C	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0045075	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0008070	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000319	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000508	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000316	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000007	PMID:35196516	PCS					I	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000219	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0002007	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0001249	PMID:35196516	PCS		12/12			P	HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000303	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619989	Neurodevelopmental disorder with speech delay and variable ocular anomalies		HP:0000369	PMID:35196516	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0002344	PMID:29618761	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0002421	PMID:29618761	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0003676	PMID:27623147	PCS					C	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0003577	PMID:27623147	PCS		2/2			C	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0002045	PMID:27623147	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001410	PMID:27485409	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001272	PMID:27485409;PMID:27623147	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001252	PMID:29618761	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0003593	PMID:27485409	PCS		2/2			C	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0003073	PMID:29618761	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001290	PMID:27485409;PMID:27623147	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0032794	PMID:27485409	PCS		1/2			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0008151	PMID:27485409	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001508	PMID:27485409	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001408	PMID:27485409	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0000817	PMID:29618761;PMID:27623147	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001943	PMID:29618761;PMID:27623147	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0002878	PMID:29618761	IEA		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0002910	PMID:27485409;PMID:29618761	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001403	PMID:27485409	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0003128	PMID:29618761;PMID:27623147	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001347	PMID:27485409	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0003348	PMID:27485409	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0008936	PMID:27623147	PCS		1/2			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001321	PMID:29618761	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0011968	PMID:27485409	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0002151	PMID:27485409	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001263	PMID:29618761;PMID:27623147	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0005484	PMID:27485409;PMID:27623147	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0030948	PMID:27485409	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0040031	PMID:29618761	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0002093	PMID:29618761	IEA		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0032988	PMID:27485409	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0000407	PMID:29618761;PMID:27623147	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001639	PMID:27485409	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0000007	PMID:27485409	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0000505	PMID:27485409	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0000648	PMID:29618761;PMID:27623147	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0001257	PMID:27485409	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-22]
OMIM:618329	Combined oxidative phosphorylation deficiency 37		HP:0003535	PMID:27485409;PMID:29618761;PMID:27623147	PCS		5/5			P	HPO:probinson[2021-09-22]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000121	PMID:8640224	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003158	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0004322	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003113	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001250	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003394	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003072	OMIM:601678	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002917	PMID:8640224	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000859	PMID:8640224	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001508	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000938	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0011461	PMID:8640224	PCS		5/5			C	HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001944	PMID:8640224	PCS	HP:0003623	5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002914	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003527	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000934	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001945	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002019	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002632	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001249	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001622	PMID:8640224	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002014	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001561	PMID:8640224	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003401	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003566	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003324	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001960	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002013	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000111	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001563	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001263	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002150	PMID:8640224	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001281	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0003081	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000848	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0001518	PMID:8640224	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000128	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000843	OMIM:601678	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000007	OMIM:601678	IEA					I	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0002900	PMID:8640224	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000103	OMIM:601678	IEA					P	HPO:iea[2009-02-17]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000127	OMIM:601678	TAS					P	HPO:skoehler[2013-10-06]
OMIM:601678	Bartter syndrome, type 1, antenatal		HP:0000841	PMID:8640224	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-01]
OMIM:118600	Chondrocalcinosis 2		HP:0005017	PMID:13130483	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:118600	Chondrocalcinosis 2		HP:0003581	PMID:13130483	PCS		11/11			C	HPO:skoehler[2012-11-16];HPO:probinson[2023-04-08]
OMIM:118600	Chondrocalcinosis 2		HP:0003040	PMID:13130483	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:118600	Chondrocalcinosis 2		HP:0002758	PMID:13130483	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:118600	Chondrocalcinosis 2		HP:0000006	PMID:12297987	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0001265	PMID:24234652	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0003577	PMID:24234652	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0001288	PMID:24234652	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0011968	PMID:24234652	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0000508	PMID:24234652	PCS		1/1		HP:0012825	P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0000007	PMID:24234652	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0003803	PMID:24234652	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0001324	PMID:24234652	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-05]
OMIM:616304	Myasthenic syndrome, congenital, 17		HP:0003403	PMID:24234652	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:155700	Melanoma, malignant familial intraocular		HP:0007716	OMIM:155700	TAS					P	HPO:probinson[2009-02-17]
OMIM:155700	Melanoma, malignant familial intraocular		HP:0000006	OMIM:155700	TAS					I	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000286	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000882	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001773	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000089	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000161	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0009381	OMIM:269860	TAS					P	HPO:skoehler[2015-02-22]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0002979	OMIM:269860	TAS					P	HPO:probinson[2012-06-03]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000316	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001405	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000238	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001769	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001643	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001169	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000358	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000695	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001541	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0011802	OMIM:269860	TAS					P	HPO:skoehler[2015-02-22]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000969	OMIM:269860	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0009099	OMIM:269860	TAS					P	HPO:probinson[2024-03-29]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000800	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000888	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000007	OMIM:269860	TAS					I	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001539	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001538	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000369	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001655	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0002323	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0002089	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001156	OMIM:269860	IEA					P	HPO:skoehler[2018-10-08]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000023	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000062	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0002240	OMIM:269860	TAS					P	HPO:skoehler[2015-02-22]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000180	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0100750	OMIM:269860	TAS					P	HPO:skoehler[2015-02-22]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0010306	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0012368	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001629	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0002557	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000774	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0006610	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000377	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000256	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000773	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001744	OMIM:269860	TAS					P	HPO:skoehler[2015-02-22]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0003026	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0009826	OMIM:269860	TAS					P	HPO:probinson[2012-06-03]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001561	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0004279	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001360	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000470	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0002093	OMIM:269860	TAS					P	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0000348	OMIM:269860	TAS					P	HPO:skoehler[2015-02-22]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0006488	OMIM:269860	TAS					P	HPO:probinson[2012-06-03]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001511	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0003811	OMIM:269860	TAS					C	HPO:probinson[2009-02-17]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0006644	OMIM:269860	IEA					P	HPO:skoehler[2015-01-27]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0002566	OMIM:269860	TAS					P	HPO:skoehler[2014-06-24]
OMIM:269860	Short-rib thoracic dysplasia 12		HP:0001831	OMIM:269860	TAS					P	HPO:skoehler[2015-02-22]
OMIM:620729	Hyperferritinemia		HP:0040133	PMID:37490907	PCS		12/12			P	HPO:probinson[2024-06-24];HPO:probinson[2024-06-24]
OMIM:620729	Hyperferritinemia		HP:0000007	PMID:37490907	PCS					I	HPO:probinson[2024-06-24]
OMIM:620729	Hyperferritinemia		HP:0040130	PMID:37490907	PCS		0/12			P	HPO:probinson[2024-06-24]
OMIM:620729	Hyperferritinemia		HP:0002910	PMID:37490907	PCS		0/12			P	HPO:probinson[2024-06-24]
OMIM:620729	Hyperferritinemia		HP:0031877	PMID:37490907	PCS		12/12			P	HPO:probinson[2024-06-24];HPO:probinson[2024-06-24]
OMIM:120200	Coloboma, ocular		HP:0000076	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0007968	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0007957	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0012521	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0000639	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0025514	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0007663	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0000568	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0000659	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0002119	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0001510	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0000006	PMID:12721955	PCS					I	HPO:probinson[2009-02-17]
OMIM:120200	Coloboma, ocular		HP:0000567	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:120200	Coloboma, ocular		HP:0000588	PMID:12721955	PCS					P	HPO:probinson[2017-12-13]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000286	OMIM:610832;PMID:17200672	PCS		11/11			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0003577	PMID:17200672	PCS		1/1			C	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0002023	PMID:17200671;PMID:17200672	PCS		2/8			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000122	PMID:17200671	PCS		1/7			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000086	PMID:17200672	PCS		1/1			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000085	PMID:17200671	PCS		1/7			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0001629	PMID:17200671	PCS		1/7			P	HPO:probinson[2013-04-01]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000957	OMIM:610832;PMID:17200672	PCS		11/11			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000316	OMIM:610832;PMID:17200672	PCS		11/11			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000953	PMID:17200671	PCS		1/7			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0008897	PMID:17200671	PCS		7/7			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0003006	PMID:17200671	PCS		1/7			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000252	OMIM:610832;PMID:17200671;PMID:17200672	PCS		16/18			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0003221	PMID:17200671;PMID:17200672	PCS		2/2			P	HPO:probinson[2024-03-19];HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000470	OMIM:610832;PMID:17200672	PCS		11/11			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0001915	OMIM:610832;PMID:17200672	PCS		11/11			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0001518	PMID:17200672	PCS		1/1			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0004808	PMID:17200671	PCS		2/7			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000007	PMID:17200671	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-24]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000568	PMID:17200671	PCS		3/7			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0009777	PMID:17200672	PCS		1/1			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0002667	PMID:17200671	PCS		3/7			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0000125	PMID:17200671	PCS		1/7			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0009778	PMID:17200671;PMID:17200672	PCS		3/8			P	HPO:probinson[2024-03-19];HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0001631	PMID:17200671	PCS		1/7			P	HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0002885	PMID:17200671	PCS		5/7			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-19]
OMIM:610832	Fanconi anemia, complementation group N		HP:0002984	PMID:17200671	PCS		2/7			P	HPO:probinson[2024-03-19]
OMIM:169600	Benign chronic pemphigus		HP:0010783	OMIM:169600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:169600	Benign chronic pemphigus		HP:0000006	OMIM:169600	IEA					I	HPO:iea[2009-02-17]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0003577	PMID:10792571;PMID:12485428	PCS		2/2			C	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0002221	PMID:10792571;PMID:12485428	PCS		1/2			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0003341	PMID:10792571	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0002293	PMID:10792571	PCS	HP:0011463	1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0002293	PMID:12485428	PCS		0/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0001805	PMID:12485428	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0008066	PMID:10792571	PCS	HP:0003577	1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0008066	PMID:12485428	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0008661	PMID:10792571	PCS	HP:0003621	1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0008400	PMID:12485428	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0000007	PMID:10792571	PCS					I	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0008404	PMID:10792571	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0006357	PMID:10792571	PCS	HP:0011462	1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0002555	PMID:10792571;PMID:12485428	PCS		1/2			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0034193	PMID:12485428	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619816	Epidermolysis bullosa, junctional 5A, intermediate		HP:0020117	PMID:10792571;PMID:12485428	PCS		2/2			P	HPO:probinson[2022-05-11]
OMIM:613485	Long QT syndrome 13		HP:0004754	PMID:20560207	PCS		3/11			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0001695	OMIM:613485	TAS					P	HPO:skoehler[2014-08-03]
OMIM:613485	Long QT syndrome 13		HP:0005184	PMID:20560207	PCS		5/10			P	HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0012664	PMID:20560207	PCS		0/9			P	HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0025708	PMID:20560207	PCS		1/2			C	HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0001635	PMID:20560207	PCS		3/9			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0001962	PMID:20560207	PCS		11/11			P	HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0001279	PMID:20560207	PCS		10/12			P	HPO:probinson[2013-06-02];HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0001664	PMID:20560207	PCS		1/11			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0000006	PMID:20560207	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0001678	PMID:20560207	PCS		1/9			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0002204	PMID:20560207	PCS		1/9			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-07-09]
OMIM:613485	Long QT syndrome 13		HP:0003623	PMID:20560207	PCS		1/2			C	HPO:probinson[2022-07-09]
OMIM:612943	Retinitis pigmentosa 42		HP:0500087	PMID:31856884	PCS		3/3			P	HPO:probinson[2022-12-21];HPO:probinson[2022-12-21]
OMIM:612943	Retinitis pigmentosa 42		HP:0003596	PMID:31856884	PCS		1/5			C	HPO:probinson[2022-12-21]
OMIM:612943	Retinitis pigmentosa 42		HP:0011462	PMID:31856884	PCS		4/5			C	HPO:probinson[2022-12-21]
OMIM:612943	Retinitis pigmentosa 42		HP:0007663	PMID:31856884	PCS		5/5			P	HPO:probinson[2022-12-21]
OMIM:612943	Retinitis pigmentosa 42		HP:0030629	PMID:31856884	PCS		3/3			P	HPO:probinson[2022-12-21];HPO:probinson[2022-12-21]
OMIM:612943	Retinitis pigmentosa 42		HP:0000510	PMID:31856884	PCS		5/5			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-12-21]
OMIM:612943	Retinitis pigmentosa 42		HP:0011505	PMID:31856884	PCS		4/5			P	HPO:probinson[2022-12-21]
OMIM:612943	Retinitis pigmentosa 42		HP:0000006	PMID:19520207	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:602588	Branchiootic syndrome 1		HP:0004467	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0000407	OMIM:602588	TAS					P	HPO:skoehler[2014-05-04]
OMIM:602588	Branchiootic syndrome 1		HP:0003828	OMIM:602588	IEA					M	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0009795	OMIM:602588	TAS					P	HPO:probinson[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0003829	OMIM:602588	IEA					I	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0008551	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0008554	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0008586	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0000378	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0000278	OMIM:602588	TAS					P	HPO:probinson[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0000410	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0000006	OMIM:602588	IEA					I	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0000369	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:602588	Branchiootic syndrome 1		HP:0004458	OMIM:602588	IEA					P	HPO:iea[2009-02-17]
OMIM:124700	Deafness, mid-tone neural		HP:0000407	OMIM:124700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:124700	Deafness, mid-tone neural		HP:0011463	OMIM:124700	IEA					C	HPO:iea[2012-07-28]
OMIM:124700	Deafness, mid-tone neural		HP:0001730	OMIM:124700	IEA					P	HPO:iea[2009-02-17]
OMIM:124700	Deafness, mid-tone neural		HP:0000006	OMIM:124700	IEA					I	HPO:iea[2009-02-17]
OMIM:217400	Corneal endothelial dystrophy and perceptive deafness		HP:0007759	OMIM:217400	IEA					P	HPO:iea[2009-02-17]
OMIM:217400	Corneal endothelial dystrophy and perceptive deafness		HP:0000407	PMID:17220209	PCS					P	HPO:probinson[2017-06-20]
OMIM:217400	Corneal endothelial dystrophy and perceptive deafness		HP:0001131	OMIM:217400	IEA					P	HPO:iea[2009-02-17]
OMIM:217400	Corneal endothelial dystrophy and perceptive deafness		HP:0011462	PMID:17220209	PCS					C	HPO:probinson[2020-09-08]
OMIM:217400	Corneal endothelial dystrophy and perceptive deafness		HP:0000007	PMID:11836359	PCS					I	HPO:iea[2009-02-17]
OMIM:217400	Corneal endothelial dystrophy and perceptive deafness		HP:0007663	PMID:17220209	PCS					P	HP:probinson[2019-02-24]
OMIM:217400	Corneal endothelial dystrophy and perceptive deafness		HP:0410280	PMID:17220209	PCS					C	HPO:probinson[2020-09-08]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001250	PMID:16055927	PCS		2/18			P	HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001251	PMID:16055927	PCS		10/18			P	HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0031964	PMID:16055927	PCS		8/18			P	HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001508	PMID:16055927	PCS		18/18			P	HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0008897	PMID:16055927	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0008734	OMIM:610198	PCS					P	HPO:probinson[2012-03-16]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001324	OMIM:610198	TAS					P	HPO:skoehler[2014-05-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0004856	PMID:16055927	PCS		12/18			P	HPO:probinson[2012-03-16];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001645	OMIM:610198	IEA					P	HPO:iea[2009-02-17]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001644	PMID:16055927	PCS		12/18			P	HPO:probinson[2012-03-16];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0031956	PMID:16055927	PCS		8/18			P	HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0003344	PMID:16055927	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0012817	OMIM:610198	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0002470	OMIM:610198	PCS					P	HPO:probinson[2012-03-16]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0009110	PMID:16055927	PCS		2/18			P	HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0000007	PMID:16055927	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001635	OMIM:610198	IEA					P	HPO:iea[2009-02-17]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001657	PMID:16055927	PCS		6/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0000648	PMID:16055927	PCS		4/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001511	PMID:16055927	PCS		8/18			P	HPO:probinson[2012-03-16];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0000047	PMID:16055927	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001631	PMID:16055927	PCS		1/18			P	HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0000028	PMID:16055927	PCS		9/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0001414	OMIM:610198	IEA					P	HPO:iea[2009-02-17]
OMIM:610198	3-methylglutaconic aciduria, type V		HP:0003535	PMID:16055927	PCS		18/18			P	HPO:probinson[2023-02-04]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0003651	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0004387	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002583	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001252	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001890	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0100721	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0012156	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001904	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001888	PMID:31554793;PMID:33054089	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002716	PMID:33054089	PCS		0/1			P	HPO:probinson[2022-06-20];HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0025435	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001945	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001742	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001744	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0040218	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0500266	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0004315	PMID:31554793;PMID:33054089	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0005425	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002014	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002850	PMID:31554793;PMID:33054089	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0000010	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0003621	PMID:31554793;PMID:33054089	PCS		2/2			C	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001880	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002851	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0004313	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002155	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001581	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0003281	PMID:33054089	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0011945	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0012312	PMID:31554793;PMID:33054089	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0012378	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0032252	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0000403	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0000964	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0000007	PMID:31554793	PCS					I	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001873	PMID:31554793;PMID:33054089	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0001433	PMID:33054089	PCS		0/1			P	HPO:probinson[2022-06-20];HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002720	PMID:31554793;PMID:33054089	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0002027	PMID:31554793	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:619802	Immunodeficiency 97 with autoinflammation		HP:0005415	PMID:31554793	IEA		1/1			P	HPO:probinson[2022-06-20]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0001276	PMID:27282648	PCS		1/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0003676	PMID:27282648	PCS					C	HPO:skoehler[2019-02-22];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002169	OMIM:614498	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002045	PMID:22279524	PCS		4/4			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002188	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0000023	OMIM:614498	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002123	PMID:27282648	PCS		1/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002063	PMID:22279524	PCS	HP:0003577	3/3			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0003593	PMID:27282648	PCS		1/2			C	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0033725	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0012332	OMIM:614498	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0100704	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0001522	PMID:22279524;PMID:27282648	PCS		5/6			C	HPO:probinson[2022-11-06];HPO:skoehler[2015-12-30];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0003688	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0003623	PMID:27282648	PCS		1/2			C	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0001347	OMIM:614498	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0000253	OMIM:614498	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0008936	PMID:27282648	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0000252	OMIM:614498	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0001662	PMID:22279524	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0003487	OMIM:614498	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0011968	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0001263	PMID:27282648	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002171	OMIM:614498	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0032663	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0010851	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0034392	PMID:27282648	PCS		2/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0031165	OMIM:614498	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002509	PMID:27282648	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002529	OMIM:614498	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0003739	PMID:22279524	PCS	HP:0030674	3/3			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0000007	PMID:22279524	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0000648	OMIM:614498	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0007359	PMID:22279524	PCS	HP:0003623	4/4			P	HPO:probinson[2022-11-06]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0000347	OMIM:614498	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:614498	Rigidity and multifocal seizure syndrome, lethal neonatal		HP:0002104	PMID:22279524;PMID:27282648	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:241120	Hypohidrosis with abnormal palmar dermal ridges		HP:0007608	OMIM:241120	IEA					P	HPO:iea[2009-02-17]
OMIM:241120	Hypohidrosis with abnormal palmar dermal ridges		HP:0000007	OMIM:241120	IEA					I	HPO:iea[2009-02-17]
OMIM:241120	Hypohidrosis with abnormal palmar dermal ridges		HP:0000966	OMIM:241120	IEA					P	HPO:iea[2009-02-17]
OMIM:241120	Hypohidrosis with abnormal palmar dermal ridges		HP:0001945	OMIM:241120	TAS					P	HPO:probinson[2009-02-17]
OMIM:241120	Hypohidrosis with abnormal palmar dermal ridges		HP:0007500	OMIM:241120	IEA					P	HPO:iea[2009-02-17]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003236	PMID:8069911;PMID:8538707	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003676	PMID:8538707	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003621	PMID:8069911;PMID:8538707	PCS		5/5			C	HPO:iea[2009-02-17];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003797	PMID:8538707	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0002650	OMIM:608099	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0001371	OMIM:608099	TAS					P	HPO:skoehler[2013-05-31]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003691	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003391	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0100297	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0008981	PMID:8069911;PMID:8538707	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0001635	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0000007	PMID:8069911	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0001638	PMID:8538707	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0002317	OMIM:608099	IEA					P	HPO:iea[2009-02-17]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0006466	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0006785	PMID:8069911	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003701	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003713	PMID:8069911	PCS		4/4			P	HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003325	PMID:8069911	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003557	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0003458	PMID:8538707	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:608099	Muscular dystrophy, limb-girdle, type 2D		HP:0001644	PMID:8538707	PCS		1/1			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:620715	Bleeding disorder, vascular-type		HP:0000132	PMID:35638551	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0011463	PMID:35638551	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0030880	PMID:35638551	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0006298	PMID:35638551	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0000007	PMID:35638551	PCS					I	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0040184	PMID:35638551	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0002239	PMID:35638551	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0000421	PMID:35638551	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:620715	Bleeding disorder, vascular-type		HP:0033505	PMID:35638551	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000286	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002188	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000122	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001134	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001252	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0003273	PMID:33159882	PCS		3/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000280	PMID:33159882	PCS		3/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000316	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002857	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000158	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000278	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001249	PMID:33159882	PCS		2/2			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000358	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000176	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0010958	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002079	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0011968	PMID:33159882	PCS		2/3			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001263	PMID:33159882	PCS		2/2			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000691	PMID:33159882	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0011927	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0010282	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0006380	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0009890	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000407	PMID:33159882	PCS		1/3			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000767	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000007	PMID:33159882	PCS					I	HPO:probinson[2021-03-30];HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0007676	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002987	PMID:33159882	PCS		3/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0009899	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000369	PMID:33159882	PCS		3/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001276	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000341	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000582	PMID:33159882	PCS		3/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0003577	PMID:33159882	PCS		4/4			C	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002002	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001274	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001270	PMID:33159882	PCS		2/2			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0003090	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0012450	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0008873	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000219	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000455	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002558	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0005306	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0001562	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000154	PMID:33159882	PCS		3/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000750	PMID:33159882	PCS		2/2			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002650	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000431	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000072	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0009907	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000470	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0002808	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000627	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0011232	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0010186	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000629	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000307	PMID:33159882	PCS		1/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0009836	PMID:33159882	PCS		2/4			P	HPO:probinson[2021-03-30]
OMIM:619194	Neurofacioskeletal syndrome with or without renal agenesis		HP:0000028	PMID:33159882	PCS		1/2			P	HPO:probinson[2021-03-30]
OMIM:133240	Esophageal ring, lower		HP:0002036	OMIM:133240	IEA					P	HPO:iea[2009-02-17]
OMIM:133240	Esophageal ring, lower		HP:0002015	OMIM:133240	IEA					P	HPO:iea[2009-02-17]
OMIM:133240	Esophageal ring, lower		HP:0000006	OMIM:133240	IEA					I	HPO:iea[2009-02-17]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0010804	PMID:29106825	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000582	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002188	PMID:29106825	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000486	PMID:29106825	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001332	PMID:29106825	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000540	PMID:29106825	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002365	PMID:29106825	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002066	PMID:29106825	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001252	PMID:29106825	PCS		4/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0003593	PMID:29106825	PCS		5/5			C	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0040082	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0033725	PMID:29106825	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000639	PMID:29106825	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000817	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001845	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000954	PMID:29106825	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000733	PMID:29106825	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002119	PMID:29106825	PCS		5/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001249	PMID:29106825	PCS		5/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001320	PMID:29106825	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000297	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002136	PMID:29106825	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001385	PMID:29106825	PCS		4/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000252	PMID:29106825	PCS		4/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000395	PMID:29106825	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001344	PMID:29106825	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002870	PMID:29106825	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0031936	PMID:29106825	PCS		4/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001288	PMID:29106825	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001761	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0011968	PMID:29106825	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002197	PMID:29106825	PCS		3/5			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001263	PMID:29106825	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002194	PMID:29106825	PCS		5/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001182	PMID:29106825	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0034295	PMID:29106825	PCS		5/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000648	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000505	PMID:29106825	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0004209	PMID:29106825	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0002307	PMID:29106825	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001257	PMID:29106825	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0000006	PMID:29106825	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter		HP:0001776	PMID:29106825	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0003577	PMID:23167593	PCS		2/2			C	HPO:probinson[2023-03-16]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000541	OMIM:212550	TAS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-03-16]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000518	OMIM:212550	IEA					P	HPO:iea[2009-02-17]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000639	OMIM:212550	IEA					P	HPO:iea[2009-02-17]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000616	OMIM:212550	IEA					P	HPO:iea[2009-02-17]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000007	PMID:23167593	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-16]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000557	PMID:23167593	PCS		1/2			P	HPO:probinson[2023-03-16]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000612	OMIM:212550	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000568	OMIM:212550	IEA	HP:0003577	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-16]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000559	PMID:23167593	PCS		1/2			P	HPO:probinson[2023-03-16]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0007401	OMIM:212550	IEA					P	HPO:skoehler[2018-10-08]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000567	OMIM:212550	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000501	OMIM:212550	TAS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-03-16]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000666	OMIM:212550	TAS					P	HPO:skoehler[2015-05-31]
OMIM:212550	Optic disc anomalies with retinal and/or macular dystrophy		HP:0000556	OMIM:212550	TAS					P	HPO:skoehler[2015-05-31]
OMIM:265900	Pyle disease		HP:0000670	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0003016	PMID:27355534	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0003621	PMID:27355534	PCS		2/4			C	HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0000684	PMID:27355534	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0001377	PMID:27355534	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0002650	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0002684	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0003581	PMID:27355534	PCS		1/4			C	HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0100255	PMID:27355534	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0002829	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0011463	PMID:27355534	PCS		1/4			C	HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0000926	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0000007	PMID:27355534	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0002738	OMIM:265900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:265900	Pyle disease		HP:0002967	PMID:27355534	PCS		1/4			P	HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0002857	PMID:27355534	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0002689	PMID:27355534	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0001324	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0006335	PMID:27355534	PCS		1/4			P	HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0000765	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0000303	OMIM:265900	IEA					P	HPO:iea[2009-02-17]
OMIM:265900	Pyle disease		HP:0004349	PMID:27355534	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:265900	Pyle disease		HP:0002753	PMID:27355534	PCS		4/4			P	HPO:probinson[2022-12-03];HPO:probinson[2022-12-03]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001773	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000486	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001250	PMID:31079900	PCS		3/5			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0012745	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000639	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0008450	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0010055	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000878	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001601	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001007	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000054	PMID:31079900	PCS		1/2			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001385	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0002079	PMID:31079900	PCS		3/5			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0002673	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0011968	PMID:31079900	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001263	PMID:31079900	PCS		5/5			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0008081	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0040022	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0004209	PMID:31079900	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000006	PMID:31079900	PCS					I	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000248	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000446	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000066	PMID:31079900	PCS		1/2			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000582	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0003577	PMID:31079900	PCS		5/5			C	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001156	PMID:31079900	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000540	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001274	PMID:31079900	PCS		1/5			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001629	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000733	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0009765	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0005824	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0001320	PMID:31079900	PCS		3/5			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000431	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0002650	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0004279	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0002373	PMID:31079900	PCS		1/5			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0005484	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000470	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0003183	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0005280	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0011304	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000826	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000506	PMID:31079900	PCS		1/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0200134	PMID:31079900	PCS		1/5			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0007018	PMID:31079900	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000028	PMID:31079900	PCS		1/2			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0000347	PMID:31079900	PCS		3/4			P	HPO:probinson[2022-12-04]
OMIM:620073	Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities		HP:0004227	PMID:31079900	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0003577	PMID:31844321	PCS		1/4			C	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0001682	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0030148	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0004970	PMID:31844321	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0025168	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0005176	PMID:31844321	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0010444	PMID:31844321	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0031664	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0033755	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0005180	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0034032	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0011463	PMID:31844321	PCS		3/4			C	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0004927	PMID:31844321	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0001647	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0000007	PMID:31844321	PCS					I	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0100749	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0001659	PMID:31844321	PCS		3/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0001962	PMID:31844321	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620067	Cardiac valvular dysplasia 2		HP:0001642	PMID:31844321	PCS		4/4			P	HPO:probinson[2022-10-02]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002069	PMID:16737835	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0001276	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003676	OMIM:252160	TAS					C	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000343	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0011935	PMID:16737835	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0011814	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0001250	OMIM:252160	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0001252	PMID:16737835	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003570	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003196	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0033725	PMID:16021469	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000639	PMID:16021469	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000737	PMID:16021469	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0012471	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000316	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002119	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000256	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003447	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003623	PMID:16737835	PCS		1/1			C	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002179	PMID:16021469	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002059	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000252	PMID:16021469	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002510	PMID:16021469	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002079	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000276	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0010934	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0011968	PMID:16737835	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000293	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003166	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0001263	PMID:16021469	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002171	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0011942	PMID:16737835	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0012019	OMIM:252160	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0001083	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0011096	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000804	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002506	PMID:16021469	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0000007	PMID:10053004	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003739	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0002007	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003811	PMID:16737835	PCS		1/1			C	HPO:probinson[2022-11-08]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0001510	OMIM:252160	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252160	Molybdenum cofactor deficiency, complementation group B		HP:0003537	PMID:16021469	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-08]
OMIM:220290	Deafness, autosomal recessive 1A		HP:0001751	OMIM:220290	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:220290	Deafness, autosomal recessive 1A		HP:0000407	OMIM:220290	TAS					P	HPO:skoehler[2012-10-14]
OMIM:220290	Deafness, autosomal recessive 1A		HP:0010984	PMID:19050930	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2021-06-21]
OMIM:220290	Deafness, autosomal recessive 1A		HP:0000007	PMID:9139825	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2022-08-13]
OMIM:180920	Aplasia of lacrimal and salivary glands		HP:0000670	OMIM:180920	IEA					P	HPO:iea[2009-02-17]
OMIM:180920	Aplasia of lacrimal and salivary glands		HP:0000217	OMIM:180920	IEA					P	HPO:iea[2009-02-17]
OMIM:180920	Aplasia of lacrimal and salivary glands		HP:0001092	OMIM:180920	IEA					P	HPO:iea[2009-02-17]
OMIM:180920	Aplasia of lacrimal and salivary glands		HP:0007732	OMIM:180920	IEA					P	HPO:iea[2012-04-01]
OMIM:180920	Aplasia of lacrimal and salivary glands		HP:0007656	OMIM:180920	IEA					P	HPO:iea[2009-02-17]
OMIM:180920	Aplasia of lacrimal and salivary glands		HP:0000006	OMIM:180920	IEA					I	HPO:iea[2009-02-17]
OMIM:312550	Retinal dysplasia, primary		HP:0001493	OMIM:312550	IEA					P	HPO:iea[2009-02-17]
OMIM:312550	Retinal dysplasia, primary		HP:0001417	OMIM:312550	IEA					I	HPO:iea[2009-02-17]
OMIM:312550	Retinal dysplasia, primary		HP:0007973	OMIM:312550	IEA					P	HPO:iea[2009-02-17]
OMIM:615962	Glucocorticoid resistance		HP:0003154	PMID:8445027	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:615962	Glucocorticoid resistance		HP:0030088	PMID:8445027	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:615962	Glucocorticoid resistance		HP:0012378	OMIM:615962	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615962	Glucocorticoid resistance		HP:0025380	PMID:8445027	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:615962	Glucocorticoid resistance		HP:0000858	OMIM:615962	TAS		1/1			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:615962	Glucocorticoid resistance		HP:0011462	PMID:8445027	PCS		1/1			C	HPO:probinson[2023-02-09]
OMIM:615962	Glucocorticoid resistance		HP:0000739	OMIM:615962	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615962	Glucocorticoid resistance		HP:0000822	OMIM:615962	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615962	Glucocorticoid resistance		HP:0000789	OMIM:615962	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615962	Glucocorticoid resistance		HP:0200114	OMIM:615962	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615962	Glucocorticoid resistance		HP:0001943	OMIM:615962	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615962	Glucocorticoid resistance		HP:0003118	PMID:8445027	PCS		3/3			P	HPO:probinson[2023-02-09]
OMIM:615962	Glucocorticoid resistance		HP:0000006	PMID:1704018	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-09]
OMIM:615962	Glucocorticoid resistance		HP:0001007	OMIM:615962	TAS					P	HPO:skoehler[2015-12-30]
OMIM:125350	Dental noneruption		HP:0006352	OMIM:125350	IEA					P	HPO:iea[2009-02-17]
OMIM:125350	Dental noneruption		HP:0000668	OMIM:125350	IEA					P	HPO:skoehler[2010-06-18]
OMIM:125350	Dental noneruption		HP:0006335	OMIM:125350	IEA					P	HPO:iea[2009-02-17]
OMIM:125350	Dental noneruption		HP:0000006	OMIM:125350	IEA					I	HPO:iea[2009-02-17]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0003577	PMID:33033404	PCS		6/6			C	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0000054	PMID:33033404	PCS		1/3			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0000750	PMID:33033404	PCS		4/4			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0031936	PMID:33033404	PCS		5/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0000243	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0001382	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0001263	PMID:33033404	PCS		6/6			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0001182	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0012510	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0009381	PMID:33033404	PCS		2/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0011451	PMID:33033404	IEA	HP:0003577	6/6			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0012450	PMID:33033404	PCS		2/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0030043	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0002119	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0004209	PMID:33033404	PCS		2/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0002307	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0001840	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0000006	PMID:33033404	PCS					I	HPO:probinson[2021-03-27];HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0000028	PMID:33033404	PCS		1/3			P	HPO:probinson[2021-03-27]
OMIM:619180	Microcephaly 27, primary, autosomal dominant		HP:0009879	PMID:33033404	PCS		1/5			P	HPO:probinson[2021-03-27]
OMIM:616258	Meckel syndrome 12		HP:0001562	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0010958	PMID:24128419	PCS		1/2			P	HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000252	PMID:24128419	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000340	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000013	PMID:24128419	PCS		2/2			P	HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000431	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000463	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0001321	PMID:24128419	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000089	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000193	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0001274	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0032464	PMID:24128419	PCS		2/4			P	HPO:probinson[2023-02-24];HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0009760	PMID:24128419	PCS		1/2			P	HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0001838	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0034198	PMID:24128419	PCS		2/2			C	HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0002804	PMID:24128419	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000007	PMID:24128419	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0006872	PMID:24128419	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0002139	PMID:24128419	PCS		1/2			P	HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0001511	PMID:24128419	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0002335	PMID:24128419	PCS		1/2			P	HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000369	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000347	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:616258	Meckel syndrome 12		HP:0000148	PMID:24128419	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-24]
OMIM:610629	Diamond-Blackfan anemia 3		HP:0011904	PMID:17186470	PCS					P	HPO:probinson[2013-04-01]
OMIM:610629	Diamond-Blackfan anemia 3		HP:0005518	PMID:17186470	PCS					P	HPO:probinson[2013-04-01]
OMIM:610629	Diamond-Blackfan anemia 3		HP:0001896	PMID:17186470	PCS					P	HPO:probinson[2013-04-01]
OMIM:610629	Diamond-Blackfan anemia 3		HP:0030270	PMID:17186470	PCS		10/10			P	HPO:probinson[2022-03-13]
OMIM:610629	Diamond-Blackfan anemia 3		HP:0001972	PMID:17186470	PCS					P	HPO:probinson[2013-01-09]
OMIM:610629	Diamond-Blackfan anemia 3		HP:0000465	PMID:17186470	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-13]
OMIM:610629	Diamond-Blackfan anemia 3		HP:0000006	PMID:17186470	PCS					I	HPO:probinson[2013-04-01]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0002421	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0003676	OMIM:617146	TAS					C	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0003236	PMID:27843126	PCS		1/5			P	HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0002540	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0004322	PMID:27843126	PCS		8/9			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001371	OMIM:617146	TAS	HP:0003577				P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0002020	PMID:27843126	PCS		2/11			P	HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001290	OMIM:617146	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001270	PMID:27843126	PCS	HP:0003593	10/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0003390	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0007340	PMID:27843126	PCS		8/9			P	HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0008872	PMID:27843126	PCS		2/11			P	HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0000219	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0000218	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001763	PMID:27843126	PCS		6/7			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001166	PMID:27843126	PCS		4/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0002058	PMID:27843126	PCS					P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0002136	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001385	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0003189	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0002650	PMID:27843126	PCS		10/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001762	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0000431	OMIM:617146	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0031936	OMIM:617146	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0003484	PMID:27843126	PCS		5/8			P	HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001260	PMID:27843126	PCS		7/7			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001263	PMID:27843126	PCS		3/9			P	HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001284	PMID:27843126	PCS		9/9			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0002093	PMID:27843126	PCS	HP:0003623	6/6			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0010871	OMIM:617146	TAS	HP:0003577				P	HPO:skoehler[2017-07-13]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0012385	PMID:27843126	PCS		6/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0007010	OMIM:617146	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0000007	PMID:27843126	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001319	PMID:27843126	PCS	HP:0003577	8/8			P	HP:probinson[2019-03-02]
OMIM:617146	Arthrogryposis, distal, with impaired proprioception and touch		HP:0001852	PMID:27843126	PCS		7/9			P	HPO:skoehler[2018-10-08];HP:probinson[2019-03-02]
OMIM:618275	Hypotrichosis 14		HP:0003577	PMID:30401459	PCS		2/2			C	HPO:probinson[2022-12-03]
OMIM:618275	Hypotrichosis 14		HP:0002221	PMID:30401459	PCS		4/6			P	HPO:probinson[2022-12-03]
OMIM:618275	Hypotrichosis 14		HP:0002231	PMID:30401459	PCS		2/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-03]
OMIM:618275	Hypotrichosis 14		HP:0010764	PMID:30401459	PCS		2/6			P	HPO:probinson[2022-12-03]
OMIM:618275	Hypotrichosis 14		HP:0000007	PMID:30401459	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-03]
OMIM:618275	Hypotrichosis 14		HP:0008070	PMID:30401459	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-03]
OMIM:618275	Hypotrichosis 14		HP:0002225	PMID:30401459	PCS		4/6			P	HPO:probinson[2022-12-03]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002663	PMID:24786642	PCS		4/4			P	HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002983	OMIM:613320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003577	PMID:24786642	PCS		4/4			C	HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0004565	PMID:24786642	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000463	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002002	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0004322	OMIM:613320	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0001591	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003177	PMID:24786642	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003196	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003175	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0011220	OMIM:613320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0008551	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0008455	OMIM:613320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000239	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002617	OMIM:613320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0008897	PMID:24786642	PCS		4/4			P	HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000774	PMID:24786642	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0001522	PMID:24786642	PCS		1/4			C	HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000311	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000773	PMID:24786642	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002657	OMIM:613320	IEA					P	HPO:skoehler[2015-12-30]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0008936	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003026	PMID:24786642	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002375	OMIM:613320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0001640	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002750	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0001263	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003021	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000470	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002092	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0005280	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003180	PMID:24786642	PCS		4/4			P	HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0003819	PMID:24786642	PCS		2/4			C	HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0001518	PMID:24786642	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000822	OMIM:613320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000007	PMID:24786642	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0006387	PMID:24786642	PCS		4/4			P	HPO:probinson[2023-05-18]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0008786	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002007	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002645	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0002789	OMIM:613320	TAS					P	HPO:skoehler[2015-06-22]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000369	OMIM:613320	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613320	Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type		HP:0000445	OMIM:613320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0003577	PMID:20827784;PMID:19797195	PCS		5/5			C	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0001162	PMID:20827784	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0000072	PMID:20827784	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0010442	PMID:19797195	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0031500	PMID:20827784	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0100543	OMIM:615989	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0000800	PMID:20827784	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0030010	PMID:20827784	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0000007	PMID:19797195	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0001830	PMID:20827784	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0000510	PMID:19797195	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0000135	PMID:19797195	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0001513	PMID:19797195	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0000126	PMID:20827784	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:615989	Bardet-Biedl syndrome 12		HP:0000148	PMID:20827784	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001298	PMID:24530203	PCS		1/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001254	PMID:24530203	PCS		3/4			P	HPO:skoehler[2014-10-06]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0033407	PMID:24530203	PCS		4/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001993	PMID:24530203	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0003572	PMID:24530203	PCS		1/3			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0002919	PMID:24530203	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0500163	PMID:24530203	PCS		1/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0011463	PMID:24530203	PCS		1/4			C	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0033111	PMID:24530203	PCS		4/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0040155	PMID:24530203	PCS		4/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001987	PMID:24530203	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001943	PMID:24530203	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0008358	PMID:24530203	PCS		4/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0003648	PMID:24530203	PCS		4/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0003228	PMID:24530203	PCS		1/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0000952	PMID:24530203	PCS		1/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001942	PMID:24530203	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0003348	PMID:24530203	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0003128	PMID:24530203	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0003623	PMID:24530203	PCS		3/4			C	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0005961	PMID:24530203	PCS		1/3			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0002572	PMID:24530203	PCS		1/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001263	OMIM:615751	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0002151	PMID:24530203	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0033213	PMID:24530203	PCS		3/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0500251	PMID:24530203	PCS		1/2			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0000007	PMID:24530203	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0003217	PMID:24530203	PCS		3/4			P	HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0001950	PMID:24530203	PCS		2/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-03]
OMIM:615751	Hyperammonemia due to carbonic anhydrase VA deficiency		HP:0002789	PMID:24530203	PCS		3/4		HP:0025303	P	HPO:skoehler[2014-10-06]
OMIM:114600	Canine teeth, absence of upper permanent		HP:0012738	OMIM:114600	TAS					P	HPO:probinson[2021-07-13]
OMIM:114600	Canine teeth, absence of upper permanent		HP:0000006	OMIM:114600	TAS					I	HPO:iea[2009-02-17]
OMIM:190500	Triphalangeal thumb with double phalanges		HP:0001199	OMIM:190500	IEA					P	HPO:iea[2009-02-17]
OMIM:190500	Triphalangeal thumb with double phalanges		HP:0009606	OMIM:190500	IEA					P	HPO:iea[2009-02-17]
OMIM:190500	Triphalangeal thumb with double phalanges		HP:0000006	OMIM:190500	IEA					I	HPO:iea[2009-02-17]
OMIM:614329	Intellectual developmental disorder, autosomal recessive 31		HP:0000007	PMID:21063731	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2025-09-26]
OMIM:614329	Intellectual developmental disorder, autosomal recessive 31		HP:0001249	PMID:21063731	PCS					P	HPO:skoehler[2013-06-16];HPO:probinson[2025-09-26]
OMIM:618513	Leber congenital amaurosis 19		HP:0000639	PMID:30573563	PCS		1/2			P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2019-09-15]
OMIM:618513	Leber congenital amaurosis 19		HP:0000007	PMID:30573563	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-15]
OMIM:618513	Leber congenital amaurosis 19		HP:0000546	PMID:30573563	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618513	Leber congenital amaurosis 19		HP:0000505	PMID:30573563	PCS	HP:0011463				P	HPO:nvasilevsky[2019-09-11]
OMIM:618513	Leber congenital amaurosis 19		HP:0000543	PMID:30573563	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-15]
OMIM:618513	Leber congenital amaurosis 19		HP:0007843	PMID:30573563	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618513	Leber congenital amaurosis 19		HP:0000654	PMID:30573563	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000341	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0002465	PMID:19716111	PCS		3/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0010747	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0002121	PMID:19716111	PCS	HP:0011463	4/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001252	PMID:19716111	PCS		3/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0002162	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0012704	PMID:19716111	PCS		2/6			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0100962	PMID:19716111	PCS		2/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000319	PMID:19716111	PCS		4/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001609	PMID:19716111	PCS		1/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0005709	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001423	PMID:19716111	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001763	PMID:19716111	PCS		3/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001249	PMID:19716111	PCS		12/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000358	PMID:19716111	PCS	HP:0003577	1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000396	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000494	PMID:19716111	PCS		2/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000750	PMID:19716111	PCS		12/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0002353	PMID:19716111	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000574	PMID:19716111	PCS		2/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000233	PMID:19716111	PCS		4/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001761	PMID:19716111	PCS		3/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000430	PMID:19716111	PCS		2/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001260	PMID:19716111	PCS		2/12			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0011800	PMID:19716111	PCS		2/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000826	PMID:19716111	PCS		7/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000426	PMID:19716111	PCS		3/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000268	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0002007	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000664	PMID:19716111	PCS		2/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0000322	PMID:19716111	PCS		3/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0006304	PMID:19716111	PCS		1/12			P	HPO:probinson[2022-10-02]
OMIM:300801	Chromosome xp11.23-p11.22 duplication syndrome		HP:0001611	PMID:19716111	PCS		1/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-02]
OMIM:601042	Dystonia 9		HP:0003401	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0000651	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0001266	OMIM:601042	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601042	Dystonia 9		HP:0001332	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0002131	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0002076	OMIM:601042	TAS					P	HPO:skoehler[2012-11-16]
OMIM:601042	Dystonia 9		HP:0001260	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0002062	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0100660	OMIM:601042	TAS					P	HPO:skoehler[2013-05-31]
OMIM:601042	Dystonia 9		HP:0100543	OMIM:601042	TAS					P	HPO:skoehler[2012-11-16]
OMIM:601042	Dystonia 9		HP:0007256	OMIM:601042	TAS					P	HPO:skoehler[2015-01-04]
OMIM:601042	Dystonia 9		HP:0001258	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0002315	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0000006	OMIM:601042	IEA					I	HPO:iea[2009-02-17]
OMIM:601042	Dystonia 9		HP:0001347	OMIM:601042	IEA					P	HPO:iea[2009-02-17]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000286	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001212	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001250	PMID:33077894	PCS		3/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0002263	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001252	PMID:33077894	PCS		5/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0410030	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0045075	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0009183	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000319	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0012471	PMID:33077894	PCS		5/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0011220	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000718	PMID:33077894	PCS		4/16			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000954	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000316	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000956	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000278	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001763	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001249	PMID:33077894	PCS		11/15			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000252	PMID:33077894	PCS		1/12			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000494	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000175	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000574	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001382	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000490	PMID:33077894	PCS		6/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001263	PMID:33077894	PCS		16/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0004691	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0011800	PMID:33077894	PCS		3/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0009890	PMID:33077894	PCS		6/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000729	PMID:33077894	PCS		9/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000722	PMID:33077894	PCS		3/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000568	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000322	PMID:33077894	PCS		3/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000325	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000369	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000006	PMID:33077894	PCS					I	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000582	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0002002	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000414	PMID:33077894	PCS		4/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000337	PMID:33077894	PCS		4/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000411	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0002558	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000256	PMID:33077894	PCS		2/12			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000336	PMID:33077894	PCS		3/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000431	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0002650	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0001288	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0003186	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0005280	PMID:33077894	PCS		4/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000709	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000508	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000307	PMID:33077894	PCS		2/32			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0000664	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0002007	PMID:33077894	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620098	Developmental delay with variable intellectual disability and dysmorphic facies		HP:0007018	PMID:33077894	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:600348	Band heterotopia		HP:0003577	PMID:28556411	PCS		1/1			C	HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0006956	PMID:28556411	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0032409	PMID:28556411;PMID:24859200	PCS		4/4			P	HPO:probinson[2023-02-10];HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0001250	PMID:28556411;PMID:24859200	PCS		4/5			P	HPO:probinson[2023-02-10];HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0001274	PMID:28556411;PMID:24859200	PCS		4/4			P	HPO:probinson[2023-02-10];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0001263	PMID:24859200	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0002282	PMID:28556411	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0012736	PMID:28556411	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0000708	OMIM:600348	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600348	Band heterotopia		HP:0000007	PMID:24859200	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0000238	PMID:24859200	PCS	HP:0003577	1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0000238	PMID:28556411	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0002119	PMID:24859200	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0001357	PMID:24859200	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0000256	PMID:24859200	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0001257	OMIM:600348	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600348	Band heterotopia		HP:0025517	PMID:24859200	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:600348	Band heterotopia		HP:0002126	PMID:28556411;PMID:24859200	PCS		4/4			P	HPO:probinson[2023-02-10];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:106210	Aniridia		HP:0003577	PMID:7550230	PCS		9/9			C	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0007759	OMIM:106210	IEA					P	HPO:iea[2009-02-17]
OMIM:106210	Aniridia		HP:0000486	PMID:16543198	PCS		4/10			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0010923	PMID:17148041	PCS		1/1			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0009918	PMID:17148041	PCS		1/1			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0031883	PMID:19034419	PCS					P	HPO:lccarmody[2018-09-25]
OMIM:106210	Aniridia		HP:0033743	PMID:7550230	PCS		1/9			P	HPO:probinson[2021-06-13]
OMIM:106210	Aniridia		HP:0012841	PMID:17148041	PCS		1/1			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0000518	PMID:7550230	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0000639	PMID:16543198	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0001488	PMID:17148041	PCS		1/1			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0200020	PMID:7550230	PCS		1/1			P	HPO:probinson[2021-03-23];HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0000577	PMID:17148041	PCS		1/1			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0002079	OMIM:106210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:106210	Aniridia		HP:0001083	PMID:16543198	PCS		1/9			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0040030	PMID:17148041	PCS		1/1			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0000609	OMIM:106210	IEA					P	HPO:iea[2009-02-17]
OMIM:106210	Aniridia		HP:0011496	PMID:16543198	PCS		5/10			P	HPO:probinson[2021-06-25]
OMIM:106210	Aniridia		HP:0000508	PMID:16543198	PCS		6/10			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0007750	PMID:16543198;PMID:17148041	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-23];HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0000526	PMID:16543198;PMID:7550230	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-23];HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0007676	PMID:17148041	PCS		1/1			P	HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0000006	PMID:7550230	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0000501	PMID:16543198;PMID:7550230	PCS		7/19			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-23];HPO:probinson[2021-03-23]
OMIM:106210	Aniridia		HP:0002126	OMIM:106210	TAS					P	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-09-25]
OMIM:106210	Aniridia		HP:0001952	PMID:19034419	PCS					P	HPO:lccarmody[2018-09-25]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0003577	PMID:23754960;PMID:23549421	PCS		6/6			C	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0025114	OMIM:615023	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0033252	PMID:23754960	PCS		5/5			P	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0012472	PMID:23549421	PCS		1/1			P	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0025092	PMID:23549421	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0000007	PMID:23549421	PCS					I	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0000656	PMID:23549421	PCS		1/1			P	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0001019	PMID:23754960;PMID:23549421	PCS		6/6			P	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0000966	PMID:23549421	PCS		1/1			P	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0040162	PMID:23549421	PCS		1/1			P	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0007479	PMID:23754960;PMID:23549421	PCS		6/6			P	HPO:probinson[2022-03-16]
OMIM:615023	Ichthyosis, congenital, autosomal recessive 9		HP:0000962	PMID:23754960	PCS		5/5			P	HPO:probinson[2022-03-16]
OMIM:154230	46,xy sex reversal 4		HP:0000582	PMID:15172006	PCS		2/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0003577	PMID:15172006	IEA		2/2			C	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0002023	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000343	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000463	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000243	PMID:15172006	PCS		2/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000815	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0008551	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0008633	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000218	PMID:15172006	PCS		2/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000059	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000457	PMID:15172006	PCS		2/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000110	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000175	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000013	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000133	PMID:15172006	PCS					P	HPO:probinson[2015-05-23];HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0001263	PMID:15172006	PCS		2/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000074	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0100263	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0012245	PMID:15172006	PCS		2/2			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000407	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000448	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000403	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000006	PMID:15172006	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0003259	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0003138	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000347	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:154230	46,xy sex reversal 4		HP:0000126	PMID:15172006	PCS		1/2			P	HPO:probinson[2022-03-24]
OMIM:227500	Factor VII deficiency		HP:0001892	OMIM:227500	IEA					P	HPO:iea[2009-02-17]
OMIM:227500	Factor VII deficiency		HP:0000132	PMID:8652821	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:227500	Factor VII deficiency		HP:0012233	OMIM:227500	TAS					P	HPO:skoehler[2013-05-31]
OMIM:227500	Factor VII deficiency		HP:0011463	PMID:8652821	PCS		1/1			C	HPO:probinson[2023-02-22]
OMIM:227500	Factor VII deficiency		HP:0008169	PMID:8652821	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:227500	Factor VII deficiency		HP:0006298	PMID:8652821	PCS		1/1			P	HPO:probinson[2023-02-22]
OMIM:227500	Factor VII deficiency		HP:0000007	PMID:8652821	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:227500	Factor VII deficiency		HP:0005261	PMID:8652821	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:227500	Factor VII deficiency		HP:0000978	PMID:8652821	PCS		1/1			P	HPO:probinson[2023-02-22]
OMIM:227500	Factor VII deficiency		HP:0002170	OMIM:227500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:227500	Factor VII deficiency		HP:0000421	PMID:8652821	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001332	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0000020	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001251	PMID:20855850	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0003593	PMID:20855850	PCS		7/10			C	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001270	OMIM:250950	IEA					P	HPO:skoehler[2010-06-18]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:6000577	PMID:3082934	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0100543	PMID:20855850	PCS					P	HPO:skoehler[2014-04-04];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001508	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0000736	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001942	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001347	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0002059	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0002510	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0000750	PMID:20855850	PCS		4/10			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0002373	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001260	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0002352	OMIM:250950	IEA					P	HPO:iea[2009-02-17]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001263	PMID:20855850	PCS		4/20			P	HPO:skoehler[2014-04-04];HPO:probinson[2020-09-19];HPO:skoehler[2019-02-22];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0003581	PMID:20855850	PCS		3/10			C	HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0000726	PMID:20855850	PCS	HP:0003581	2/10			P	HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0000007	PMID:20855850	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0000648	PMID:20855850	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0002305	PMID:20855850	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0001257	PMID:20855850	PCS		2/10			P	HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0002500	PMID:20855850	PCS		4/6			P	HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0003535	PMID:20855850	PCS		10/10			P	HPO:skoehler[2015-01-19];HPO:probinson[2020-09-19]
OMIM:250950	3-methylglutaconic aciduria, type I		HP:0000742	PMID:20855850	PCS		1/10			P	HPO:probinson[2020-09-19]
OMIM:615745	Atrial standstill 2		HP:0001297	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0001662	OMIM:615745	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615745	Atrial standstill 2		HP:0025478	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0001692	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0200127	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0002094	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0100699	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0033122	PMID:23275345	PCS					P	HPO:probinson[2020-10-12]
OMIM:615745	Atrial standstill 2		HP:0000007	PMID:23275345	PCS					I	HPO:skoehler[2015-12-30]
OMIM:615745	Atrial standstill 2		HP:0002617	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0001638	OMIM:615745	IEA					P	HPO:skoehler[2015-01-27]
OMIM:615745	Atrial standstill 2		HP:0001962	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0006698	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:615745	Atrial standstill 2		HP:0003238	PMID:23275345	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002421	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0000341	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001254	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0003676	OMIM:611523	TAS					C	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0003577	PMID:17847012	PCS		3/3			C	HPO:skoehler[2012-11-20];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0000189	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001250	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002120	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001272	PMID:17847012	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001252	OMIM:611523	TAS					P	HPO:skoehler[2014-11-26]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002020	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002061	OMIM:611523	TAS					P	HPO:skoehler[2012-11-20]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001290	PMID:17847012	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0012444	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001508	PMID:17847012	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0007366	OMIM:611523	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001347	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0000253	OMIM:611523	TAS					P	HPO:skoehler[2013-01-22]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001320	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0008936	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0000252	PMID:17847012	PCS		1/3			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002059	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001344	OMIM:611523	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001321	PMID:17847012	PCS		1/3			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002197	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0011968	PMID:17847012	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0011924	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002033	PMID:17847012	PCS		2/3			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0000490	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002151	PMID:17847012	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002490	PMID:17847012	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0012736	PMID:17847012	PCS		3/3			P	HPO:probinson[2022-10-21];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0011923	PMID:17847012	PCS		2/3			P	HPO:probinson[2022-10-21];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0003819	OMIM:611523	TAS					C	HPO:skoehler[2012-11-20]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0034353	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0000426	OMIM:611523	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0000007	PMID:17847012	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0008347	PMID:17847012	PCS		2/3			P	HPO:probinson[2022-10-21];HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0001257	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0006986	OMIM:611523	TAS					P	HPO:skoehler[2012-11-20]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0034391	PMID:17847012	PCS		1/3			P	HPO:probinson[2022-10-21]
OMIM:611523	Pontocerebellar hypoplasia, type 6		HP:0002104	PMID:17847012	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-21]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0001442	OMIM:607341	TAS					I	HPO:skoehler[2017-07-13]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0002384	OMIM:607341	TAS					P	HPO:probinson[2009-02-17]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0003581	OMIM:607341	IEA					C	HPO:iea[2009-02-17]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0003593	OMIM:607341	IEA					C	HPO:iea[2009-02-17]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0100543	OMIM:607341	TAS					P	HPO:probinson[2012-07-20]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0032051	PMID:25799227	PCS					P	HPO:nvasilevsky[2018-09-17]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0007042	OMIM:607341	IEA					P	HPO:iea[2009-02-17]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0002539	OMIM:607341	IEA					P	HPO:skoehler[2015-01-19]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0001269	OMIM:607341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0003745	OMIM:607341	TAS					I	HPO:iea[2009-02-17]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0001249	OMIM:607341	TAS					P	HPO:skoehler[2015-12-30]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0007206	PMID:22497611	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:607341	Focal cortical dysplasia of taylor		HP:0002446	OMIM:607341	TAS					P	HPO:probinson[2009-02-17]
OMIM:223000	Lactase deficiency, congenital		HP:0002014	PMID:16400612	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-23]
OMIM:223000	Lactase deficiency, congenital		HP:0025130	PMID:16400612	PCS	HP:0003577				P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:223000	Lactase deficiency, congenital		HP:0001944	PMID:16400612	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:223000	Lactase deficiency, congenital		HP:0000007	PMID:16400612	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:223000	Lactase deficiency, congenital		HP:0001942	PMID:16400612	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:223000	Lactase deficiency, congenital		HP:0004789	PMID:16400612	PCS					P	HPO:probinson[2013-03-10];HPO:probinson[2022-05-23]
OMIM:223000	Lactase deficiency, congenital		HP:0003623	PMID:16400612	PCS					C	HPO:probinson[2022-05-23]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0032170	PMID:28011864	PCS		1/4			P	HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0004313	PMID:28011864	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0005523	PMID:28011864	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0012189	PMID:28011863;PMID:28011864	PCS		4/5			P	HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0410297	PMID:28011864	PCS		2/3			P	HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0002719	PMID:28011864	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0000007	PMID:28011864	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0002716	PMID:28011863;PMID:28011864	PCS		11/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-10-26];HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0001954	PMID:28011863	PCS		1/1			P	HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0001433	PMID:28011863	PCS		1/1			P	HPO:probinson[2020-10-26]
OMIM:618261	Lymphoproliferative syndrome 3		HP:0040218	PMID:28011863	PCS		1/1			P	HPO:probinson[2020-10-26]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0000121	OMIM:614473	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0030149	PMID:16573612	PCS		2/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0001640	PMID:16573612	PCS		2/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0003593	PMID:16573612	PCS		2/2			C	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0030718	PMID:16573612	PCS		1/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0011703	PMID:16573612	PCS		1/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0012664	PMID:16573612	PCS		2/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0005180	PMID:16573612	PCS		1/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0001717	PMID:16573612	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0001658	PMID:16573612	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0000822	OMIM:614473	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0001635	PMID:16573612	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0000007	PMID:16573612	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0004912	OMIM:614473	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0001653	PMID:16573612	PCS		1/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:614473	Arterial calcification, generalized, of infancy, 2		HP:0003207	PMID:16573612	PCS		2/2			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:601718	Retinitis pigmentosa 19		HP:0001133	PMID:9070931	PCS					P	HPO:skoehler[2015-07-20]
OMIM:601718	Retinitis pigmentosa 19		HP:0007737	OMIM:601718	TAS					P	HPO:skoehler[2013-01-09]
OMIM:601718	Retinitis pigmentosa 19		HP:0000662	PMID:9070931	PCS	HP:0003621				P	HPO:skoehler[2015-07-20]
OMIM:601718	Retinitis pigmentosa 19		HP:0000007	PMID:9425888	PCS					I	HPO:probinson[2015-07-19]
OMIM:601718	Retinitis pigmentosa 19		HP:0007663	OMIM:601718	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601718	Retinitis pigmentosa 19		HP:0000505	PMID:9070931	PCS	HP:0003621				P	HPO:skoehler[2015-07-20]
OMIM:601718	Retinitis pigmentosa 19		HP:0000510	OMIM:601718	TAS					P	HPO:skoehler[2013-01-09]
OMIM:601718	Retinitis pigmentosa 19		HP:0000543	OMIM:601718	TAS					P	HPO:skoehler[2013-01-09]
OMIM:601718	Retinitis pigmentosa 19		HP:0007843	OMIM:601718	TAS					P	HPO:skoehler[2013-01-09]
OMIM:601718	Retinitis pigmentosa 19		HP:0007722	OMIM:601718	TAS					P	HPO:skoehler[2015-07-20]
OMIM:601718	Retinitis pigmentosa 19		HP:0000512	PMID:9070931	PCS					P	HPO:skoehler[2015-07-20]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0002069	PMID:30269351	PCS		12/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0002136	PMID:30269351	PCS		6/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0000252	PMID:30269351	PCS		3/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0000750	PMID:30269351	PCS		24/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0001332	PMID:30269351	PCS		3/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0002376	PMID:30269351	PCS		2/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0031936	PMID:30269351	PCS		8/22			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0001250	PMID:30269351	PCS		15/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0002121	PMID:30269351	PCS		5/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0001252	PMID:30269351	PCS		8/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0001263	PMID:30269351	PCS		24/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0003593	PMID:30269351	PCS					C	HPO:probinson[2021-03-06];HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0032794	PMID:30269351	PCS		7/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0011182	PMID:30269351	PCS		9/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0002719	PMID:30269351	PCS		2/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0011463	PMID:30269351	PCS					C	HPO:probinson[2021-03-06];HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0000718	PMID:30269351	PCS		4/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0000729	PMID:30269351	PCS		12/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0000964	PMID:30269351	PCS		3/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0007359	PMID:30269351	PCS		5/24			P	HPO:probinson[2021-03-06];HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0007018	PMID:30269351	PCS		4/24			P	HPO:probinson[2021-03-06]
OMIM:619157	Neurodevelopmental disorder with or without early-onset generalized epilepsy		HP:0000006	PMID:30269351	PCS					I	HPO:probinson[2021-03-06];HPO:probinson[2021-03-06]
OMIM:107640	Apnea, central sleep		HP:0000006	OMIM:107640	TAS					I	HPO:skoehler[2009-02-17]
OMIM:107640	Apnea, central sleep		HP:0010535	OMIM:107640	TAS					P	HPO:skoehler[2010-06-20]
OMIM:107640	Apnea, central sleep		HP:0001699	OMIM:107640	TAS					P	HPO:skoehler[2013-02-25]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002421	PMID:25901006	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002465	PMID:25901006	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0000365	PMID:25901006	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0001272	PMID:25901006	PCS		1/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002020	PMID:25901006	PCS		1/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0003593	PMID:25901006	PCS		2/2			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002061	PMID:25901006	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0001508	PMID:25901006	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0000817	PMID:25901006	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0000514	PMID:25901006	PCS		1/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0003348	PMID:25901006	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0008936	PMID:25901006	PCS		2/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002078	PMID:25901006	PCS		1/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0001266	PMID:25901006	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002197	PMID:25901006	PCS		1/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0001263	PMID:25901006	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002151	PMID:25901006	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0011923	PMID:25901006	PCS		2/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0100660	PMID:25901006	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0007256	PMID:25901006	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0000007	PMID:25901006	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0000648	PMID:25901006	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0002304	PMID:25901006	PCS		1/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0000543	PMID:25901006	PCS		2/2			P	HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0003677	PMID:25901006	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:618249	Mitochondrial complex I deficiency, nuclear type 28		HP:0001138	PMID:25901006	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-10]
OMIM:600360	Aplasia cutis congenita of limbs, recessive		HP:0007506	OMIM:600360	TAS					P	HPO:probinson[2009-02-17]
OMIM:600360	Aplasia cutis congenita of limbs, recessive		HP:0001057	OMIM:600360	TAS					P	HPO:probinson[2009-02-17]
OMIM:600360	Aplasia cutis congenita of limbs, recessive		HP:0000007	OMIM:600360	IEA					I	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001374	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003236	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002983	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003552	PMID:16927315	PCS		18/18			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0004322	PMID:16927315;PMID:11941538	PCS		17/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000160	PMID:11941538	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003273	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000482	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003593	PMID:16927315;PMID:11941538	PCS		8/21			C	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000518	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0011463	PMID:16927315;PMID:11941538	PCS		11/21			C	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0006473	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002938	PMID:11941538	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002979	PMID:16927315;PMID:11941538	PCS		5/21			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000316	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002812	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0008734	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001324	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001763	PMID:16927315;PMID:11941538	PCS		3/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001249	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001265	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002751	PMID:16927315;PMID:11941538	PCS		2/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003202	PMID:11941538	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002673	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002750	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000298	PMID:16927315	PCS		18/18			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000293	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002230	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003044	OMIM:255800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000926	OMIM:255800	IEA		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001537	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000007	PMID:11101850	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002947	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000205	PMID:11941538	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000768	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003712	PMID:11941538	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000369	PMID:11941538	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002047	OMIM:255800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003577	PMID:16927315	PCS		2/18			C	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003016	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003731	PMID:11941538	PCS		2/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0005830	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002002	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000023	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003177	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000581	PMID:11941538	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0010548	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0012368	OMIM:255800	TAS					P	HPO:skoehler[2013-10-22]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000939	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0011120	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0007740	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002515	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0006499	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000218	PMID:11941538	PCS		2/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001621	OMIM:255800	TAS					P	HPO:probinson[2013-04-12]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001620	OMIM:255800	TAS					P	HPO:probinson[2013-04-12]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000396	PMID:11941538	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0002650	PMID:16927315	PCS		10/18			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001762	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000272	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000470	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0100284	PMID:11941538	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0045025	PMID:11941538	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0009473	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000508	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0001239	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0006487	PMID:11941538	PCS		2/3			P	HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0003417	PMID:11941538	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000347	PMID:11941538	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:255800	Schwartz-jampel syndrome, type 1		HP:0000545	OMIM:255800	IEA					P	HPO:iea[2009-02-17]
OMIM:606711	Specific language impairment 1		HP:0000750	OMIM:606711	IEA					P	HPO:iea[2009-02-17]
OMIM:606711	Specific language impairment 1		HP:0002463	OMIM:606711	TAS					P	HPO:skoehler[2015-01-21]
OMIM:606711	Specific language impairment 1		HP:0001426	OMIM:606711	IEA					I	HPO:iea[2009-02-17]
OMIM:606711	Specific language impairment 1		HP:0002526	OMIM:606711	IEA					P	HPO:iea[2009-02-17]
OMIM:606711	Specific language impairment 1		HP:0002549	OMIM:606711	IEA					P	HPO:iea[2009-02-17]
OMIM:616502	Cone-rod dystrophy 21		HP:0000662	PMID:25983245	PCS		HP:0040283			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-04-22]
OMIM:616502	Cone-rod dystrophy 21		HP:0011462	PMID:25983245	PCS					C	HPO:probinson[2023-04-22]
OMIM:616502	Cone-rod dystrophy 21		HP:0000613	PMID:25983245	PCS		HP:0040283			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-04-22]
OMIM:616502	Cone-rod dystrophy 21		HP:0000007	PMID:25983245	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-22]
OMIM:616502	Cone-rod dystrophy 21		HP:0007663	PMID:25983245	PCS					P	HPO:skoehler[2015-08-05];HPO:probinson[2023-04-22]
OMIM:616502	Cone-rod dystrophy 21		HP:0007401	PMID:25983245	PCS					P	HPO:skoehler[2015-08-05];HPO:probinson[2023-04-22]
OMIM:616502	Cone-rod dystrophy 21		HP:0000556	PMID:25983245	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-22]
OMIM:218900	Crome syndrome		HP:0000252	PMID:14065995	PCS		2/2			P	HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0004322	PMID:14065995	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0000639	PMID:14065995	PCS	HP:0003593	1/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0001250	PMID:14065995	PCS	HP:0003593	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0008682	PMID:14065995	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0007033	PMID:14065995	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0000519	PMID:14065995	PCS	HP:0003577	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0000007	PMID:14065995	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0011344	PMID:14065995	PCS	HP:0003577	2/2			P	HPO:probinson[2020-02-23];HPO:probinson[2020-02-23]
OMIM:218900	Crome syndrome		HP:0001249	PMID:14065995	PCS	HP:0003593	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-23]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0002983	OMIM:608728	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0003016	PMID:15121775	PCS					P	HPO:probinson[2012-06-10];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, matrilin-3 related		HP:0003577	PMID:15121775	PCS		1/5			C	HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0001377	PMID:15121775	PCS		2/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0002980	PMID:15121775	PCS		1/5			P	HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0005257	PMID:15121775	PCS		1/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, matrilin-3 related		HP:0003375	PMID:15121775	PCS					P	HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, matrilin-3 related		HP:0003177	PMID:15121775	PCS					P	HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, matrilin-3 related		HP:0003593	PMID:15121775	PCS		4/5			C	HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0005054	PMID:15121775	PCS					P	HPO:probinson[2012-06-10];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0003173	PMID:15121775	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0010585	PMID:15121775	PCS					P	HPO:probinson[2012-06-18];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0012368	PMID:15121775	PCS		1/5			P	HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0008794	PMID:15121775	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0002938	PMID:15121775	PCS		4/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0008873	PMID:15121775	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0002979	PMID:15121775	PCS		4/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0002515	PMID:15121775	PCS		4/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0003026	PMID:15121775	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0002651	PMID:15121775	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0003300	PMID:15121775	PCS					P	HPO:probinson[2012-07-29]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0003180	PMID:15121775	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0010582	PMID:15121775	PCS					P	HPO:probinson[2012-06-18];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0000926	PMID:15121775	PCS					P	HPO:probinson[2012-07-29]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0000767	PMID:15121775	PCS		1/5			P	HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0000007	PMID:15121775	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:608728	Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type		HP:0000922	PMID:15121775	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-15]
OMIM:606705	Deafness, autosomal dominant 36		HP:0003621	PMID:11850618	PCS					C	HPO:probinson[2023-03-16]
OMIM:606705	Deafness, autosomal dominant 36		HP:0000407	PMID:11850618	PCS	HP:0003621				P	HPO:probinson[2013-02-23];HPO:probinson[2023-03-16]
OMIM:606705	Deafness, autosomal dominant 36		HP:0000360	OMIM:606705	TAS					P	HPO:skoehler[2015-04-05]
OMIM:606705	Deafness, autosomal dominant 36		HP:0000006	PMID:11850618	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-03-16]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0003236	OMIM:616516	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0003676	OMIM:616516	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0002155	OMIM:616516	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0002650	OMIM:616516	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0001288	PMID:10739764	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-04]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0003141	OMIM:616516	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0003560	OMIM:616516	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0011675	OMIM:616516	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0034392	PMID:10739764	PCS	HP:0003581	1/1			P	HPO:probinson[2022-11-04]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0011463	PMID:10739764	PCS		1/1			C	HPO:probinson[2022-11-04]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0000007	PMID:10739764	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0002505	PMID:10739764	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0001324	OMIM:616516	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0002987	OMIM:616516	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616516	Emery-Dreifuss muscular dystrophy 3, autosomal recessive		HP:0003700	PMID:10739764	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0003577	PMID:33058759	IEA		4/4			C	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0010804	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0001156	PMID:33058759	PCS		2/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0002002	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0002164	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0005274	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000316	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0006695	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000337	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0002857	PMID:33058759	PCS		2/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000774	PMID:33058759	PCS		2/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000698	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0009826	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000276	PMID:33058759	PCS		2/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0001162	PMID:33058759	PCS		4/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0005001	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0011565	PMID:33058759	PCS	HP:0003577	3/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000191	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0011670	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000668	PMID:33058759	PCS		2/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0001217	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0100818	PMID:33058759	PCS		2/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0004209	PMID:33058759	PCS		2/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0001830	PMID:33058759	PCS		3/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000322	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000006	PMID:33058759	PCS					I	HPO:probinson[2021-01-16];HPO:probinson[2021-01-16]
OMIM:619143	Cardioacrofacial dysplasia 2		HP:0000303	PMID:33058759	PCS		1/4			P	HPO:probinson[2021-01-16]
OMIM:616270	Amelogenesis imperfecta, type IF		HP:0011073	PMID:26502894	IEA		1/1			P	HPO:skoehler[2015-09-16];HPO:probinson[2021-02-20]
OMIM:616270	Amelogenesis imperfecta, type IF		HP:0000705	PMID:26502894;PMID:24858907	PCS		4/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2021-02-20];HPO:probinson[2021-02-20]
OMIM:616270	Amelogenesis imperfecta, type IF		HP:0006297	PMID:26502894;PMID:24858907	PCS		4/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2021-02-20];HPO:probinson[2021-02-20]
OMIM:616270	Amelogenesis imperfecta, type IF		HP:0003593	PMID:24858907	PCS					C	HPO:probinson[2021-02-20]
OMIM:616270	Amelogenesis imperfecta, type IF		HP:0000007	PMID:24858907	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2021-02-20]
OMIM:616270	Amelogenesis imperfecta, type IF		HP:0009722	PMID:24858907	PCS					P	HPO:skoehler[2015-09-16];HPO:probinson[2021-02-20]
OMIM:158350	Cowden syndrome 1		HP:0000365	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0030731	OMIM:158350	IEA					P	HPO:skoehler[2018-10-08]
OMIM:158350	Cowden syndrome 1		HP:0000221	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0001250	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000160	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0010609	OMIM:158350	TAS					P	HPO:skoehler[2010-06-20]
OMIM:158350	Cowden syndrome 1		HP:0200016	OMIM:158350	TAS					P	HPO:probinson[2017-05-17]
OMIM:158350	Cowden syndrome 1		HP:0001031	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0004481	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0002080	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0012871	OMIM:158350	TAS					P	HPO:skoehler[2014-06-24]
OMIM:158350	Cowden syndrome 1		HP:0000518	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0002719	OMIM:158350	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:158350	Cowden syndrome 1		HP:0000836	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0100646	OMIM:158350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158350	Cowden syndrome 1		HP:0002858	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000854	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0001888	OMIM:158350	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:158350	Cowden syndrome 1		HP:0000218	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000972	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0001249	OMIM:158350	TAS					P	HPO:skoehler[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000853	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000138	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0007206	PMID:22497611	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:158350	Cowden syndrome 1		HP:0025318	OMIM:158350	IEA					P	HPO:skoehler[2017-07-13]
OMIM:158350	Cowden syndrome 1		HP:0002597	OMIM:158350	TAS					P	HPO:probinson[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0004313	OMIM:158350	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:158350	Cowden syndrome 1		HP:0003002	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0002650	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0001102	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000771	OMIM:158350	TAS					P	HPO:skoehler[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000034	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0500009	OMIM:158350	IEA					P	HPO:skoehler[2017-07-13]
OMIM:158350	Cowden syndrome 1		HP:0002253	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0003581	OMIM:158350	TAS					C	HPO:skoehler[2013-12-21]
OMIM:158350	Cowden syndrome 1		HP:0001263	OMIM:158350	IEA					P	HPO:skoehler[2017-07-13]
OMIM:158350	Cowden syndrome 1		HP:0010619	OMIM:158350	TAS					P	HPO:skoehler[2015-08-05]
OMIM:158350	Cowden syndrome 1		HP:0004390	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0002808	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000767	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000327	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000821	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0006740	OMIM:158350	TAS					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000545	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000347	OMIM:158350	IEA					P	HPO:iea[2009-02-17]
OMIM:158350	Cowden syndrome 1		HP:0000006	OMIM:158350	IEA					I	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0001397	PMID:15384098	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0003774	PMID:15384098	PCS	HP:0011463	5/5			P	HPO:probinson[2014-01-18];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0002365	OMIM:243910	TAS					P	HPO:probinson[2014-03-12]
OMIM:243910	Arima syndrome		HP:0005576	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0012606	PMID:15384098	PCS		5/5			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0001395	PMID:15384098	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0001252	PMID:15384098	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0001251	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0002240	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0001394	PMID:15384098	PCS		3/4			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0001290	OMIM:243910	TAS					P	HPO:skoehler[2017-07-13]
OMIM:243910	Arima syndrome		HP:0002282	OMIM:243910	IEA					P	HPO:skoehler[2010-06-20]
OMIM:243910	Arima syndrome		HP:0002040	PMID:15384098	PCS					P	HPO:probinson[2022-10-06];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000639	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0001903	PMID:15384098	PCS		5/5			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000618	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0002419	PMID:15384098	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0002436	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0000113	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0002335	OMIM:243910	TAS					P	HPO:skoehler[2009-02-17]
OMIM:243910	Arima syndrome		HP:0000556	PMID:15384098	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000550	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0000154	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0001320	PMID:15384098	PCS		5/5			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0001162	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0002198	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0001263	OMIM:243910	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-06];HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0000790	PMID:15384098	PCS		1/3			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0002094	OMIM:243910	IEA					P	HPO:skoehler[2010-06-20]
OMIM:243910	Arima syndrome		HP:0000090	OMIM:243910	TAS	HP:0003621				P	HPO:probinson[2014-01-18]
OMIM:243910	Arima syndrome		HP:0000093	PMID:15384098	PCS		1/3			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000092	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0001959	PMID:15384098	PCS		3/3			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0002508	OMIM:243910	TAS					P	HPO:skoehler[2014-03-24]
OMIM:243910	Arima syndrome		HP:0000508	PMID:15384098	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000822	PMID:15384098	PCS		2/5			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000007	OMIM:243910	IEA					I	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0000648	PMID:15384098	PCS		3/5			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000108	PMID:15384098	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0001830	OMIM:243910	IEA					P	HPO:iea[2009-02-17]
OMIM:243910	Arima syndrome		HP:0000103	PMID:15384098	PCS		3/3			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0002789	OMIM:243910	IEA					P	HPO:skoehler[2010-06-20]
OMIM:243910	Arima syndrome		HP:0001510	PMID:15384098	PCS		4/5			P	HPO:probinson[2022-10-06]
OMIM:243910	Arima syndrome		HP:0000567	PMID:15384098	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:115250	Collagenoma, familial cutaneous		HP:0001089	OMIM:115250	IEA					P	HPO:iea[2009-02-17]
OMIM:115250	Collagenoma, familial cutaneous		HP:6000022	OMIM:115250	TAS					P	HPO:probinson[2024-01-06]
OMIM:115250	Collagenoma, familial cutaneous		HP:0000407	OMIM:115250	IEA					P	HPO:iea[2009-02-17]
OMIM:115250	Collagenoma, familial cutaneous		HP:0005110	OMIM:115250	IEA					P	HPO:iea[2009-02-17]
OMIM:115250	Collagenoma, familial cutaneous		HP:0001635	OMIM:115250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:115250	Collagenoma, familial cutaneous		HP:0001638	OMIM:115250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:115250	Collagenoma, familial cutaneous		HP:0008720	OMIM:115250	IEA					P	HPO:iea[2009-02-17]
OMIM:115250	Collagenoma, familial cutaneous		HP:0011663	OMIM:115250	TAS					P	HPO:skoehler[2013-06-11]
OMIM:115250	Collagenoma, familial cutaneous		HP:0007534	OMIM:115250	IEA					P	HPO:iea[2009-02-17]
OMIM:115250	Collagenoma, familial cutaneous		HP:0000006	OMIM:115250	IEA					I	HPO:iea[2009-02-17]
OMIM:115250	Collagenoma, familial cutaneous		HP:0005180	OMIM:115250	IEA					P	HPO:iea[2009-02-17]
OMIM:115250	Collagenoma, familial cutaneous		HP:0002633	OMIM:115250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0100512	OMIM:613308	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0003577	PMID:20116044	PCS		1/4			C	HPO:probinson[2022-11-08]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0003621	PMID:20116044	PCS		1/4			C	HPO:probinson[2022-11-08]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0001903	PMID:20116044	PCS		5/5			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-11-08]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0003593	PMID:20116044	PCS		2/4			C	HPO:probinson[2022-11-08]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0001510	OMIM:613308	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0000465	PMID:20116044	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:613308	Diamond-Blackfan anemia 9		HP:0000006	PMID:20116044	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0000486	PMID:18319072	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001272	PMID:18319072	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001250	OMIM:612016	TAS		2/2			P	HPO:skoehler[2012-11-28];HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001252	PMID:18319072	PCS		1/2			P	HPO:skoehler[2014-11-26]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001251	PMID:18319072	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0003593	PMID:18319072	PCS		1/2			C	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0032653	PMID:18319072	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0012847	PMID:18319072	PCS		2/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0011463	PMID:18319072	PCS		1/2			C	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0003701	PMID:18319072	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001249	OMIM:612016	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0003546	OMIM:612016	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001347	OMIM:612016	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0003128	OMIM:612016	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0008936	PMID:18319072	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001761	OMIM:612016	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0010818	PMID:18319072	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001263	OMIM:612016	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0002151	PMID:18319072	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0002490	PMID:18319072	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0034369	PMID:18319072	PCS					P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0012240	PMID:18319072	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0000508	PMID:18319072	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0007256	OMIM:612016	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0000007	PMID:18319072	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-29]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001337	OMIM:612016	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612016	Coenzyme Q10 deficiency, primary, 4		HP:0001336	OMIM:612016	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0001650	PMID:24702954	PCS		1/10			P	HPO:skoehler[2014-08-24]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0003577	PMID:24702954	PCS		10/10			C	HPO:probinson[2023-04-08]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0001629	PMID:24702954	PCS		1/10			P	HPO:skoehler[2014-08-24]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0001680	PMID:24702954	PCS		1/10			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-08]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0004383	PMID:24702954	PCS		1/10			P	HPO:skoehler[2014-08-24]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0001636	PMID:24702954	PCS		1/10			P	HPO:skoehler[2014-08-24]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0006695	PMID:24702954	PCS		6/10			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-08]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0000006	PMID:24702954	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-08]
OMIM:615779	Congenital heart defects, multiple types, 4		HP:0032092	PMID:24702954	PCS		2/10			P	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:191150	Tuftsin deficiency		HP:0002719	OMIM:191150	IEA					P	HPO:skoehler[2009-02-17]
OMIM:191150	Tuftsin deficiency		HP:0000006	OMIM:191150	IEA					I	HPO:iea[2009-02-17]
OMIM:191150	Tuftsin deficiency		HP:0001743	OMIM:191150	IEA					P	HPO:skoehler[2009-02-17]
OMIM:236800	Hydroxykynureninuria		HP:6000121	PMID:17334708	PCS		1/1			P	HPO:probinson[2024-02-09]
OMIM:236800	Hydroxykynureninuria		HP:0002013	PMID:17334708	PCS	HP:0003623	1/1			P	HPO:probinson[2022-06-23]
OMIM:236800	Hydroxykynureninuria		HP:6000265	PMID:17334708	PCS		1/1			P	HPO:probinson[2024-02-09]
OMIM:236800	Hydroxykynureninuria		HP:0000007	PMID:17334708	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:236800	Hydroxykynureninuria		HP:0000952	PMID:17334708	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:236800	HYDROXYKYNURENINURIA		HP:0003623	PMID:17334708	PCS		1/1			C	HPO:probinson[2022-06-23]
OMIM:611090	Intellectual developmental disorder, autosomal recessive 12		HP:0000007	OMIM:611090	TAS					I	HPO:probinson[2013-01-09]
OMIM:611090	Intellectual developmental disorder, autosomal recessive 12		HP:0001249	OMIM:611090	TAS					P	HPO:probinson[2013-04-01]
OMIM:301060	Azoospermia, obstructive, with nephrolithiasis		HP:0033808	PMID:31320686	PCS		3/3			P	HPO:probinson[2021-05-08]
OMIM:301060	Azoospermia, obstructive, with nephrolithiasis		HP:0001419	PMID:31320686	PCS					I	HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:301060	Azoospermia, obstructive, with nephrolithiasis		HP:0003251	PMID:31320686	PCS		9/9			P	HPO:probinson[2021-05-08]
OMIM:301060	Azoospermia, obstructive, with nephrolithiasis		HP:0011962	PMID:31320686	PCS		3/3			P	HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:301060	Azoospermia, obstructive, with nephrolithiasis		HP:0000787	PMID:31320686	PCS		3/3			P	HPO:probinson[2021-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0002224	PMID:24671081	PCS		2/7			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0002231	PMID:24671081	PCS		7/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0002209	PMID:24671081	PCS		7/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0009775	PMID:24671081	PCS					P	HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0000007	PMID:24671081	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0000653	PMID:24671081	PCS		7/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0000982	PMID:24671081	PCS		7/7			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0045075	PMID:24671081	PCS		7/7			P	HPO:probinson[2022-05-08]
OMIM:616099	Palmoplantar keratoderma and woolly hair		HP:0001820	PMID:24671081	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-08]
OMIM:245150	Keutel syndrome		HP:0000365	PMID:15810001	PCS		12/17			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0002002	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0010109	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0001250	PMID:15810001	PCS		5/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0005275	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0001629	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0001507	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0009882	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0002837	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0002514	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0001642	OMIM:245150	TAS					P	HPO:skoehler[2015-01-21]
OMIM:245150	Keutel syndrome		HP:0006536	OMIM:245150	IEA					P	HPO:skoehler[2018-10-08]
OMIM:245150	Keutel syndrome		HP:0006118	PMID:15810001	PCS		20/20			P	HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0000431	PMID:15810001	PCS		15/15			P	HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0005103	PMID:15810001	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0000276	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0005268	OMIM:245150	IEA					C	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0004971	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0001263	PMID:15810001	PCS		10/17			P	HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0002097	OMIM:245150	IEA					P	HPO:skoehler[2018-10-08]
OMIM:245150	Keutel syndrome		HP:0000272	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0011800	PMID:15810001	PCS		12/12		HP:0012825	P	HPO:skoehler[2013-11-28];HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0011109	OMIM:245150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245150	Keutel syndrome		HP:0005280	PMID:15810001	PCS		15/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0010655	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0006140	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0000822	OMIM:245150	IEA					P	HPO:skoehler[2018-10-08]
OMIM:245150	Keutel syndrome		HP:0000007	PMID:9916809	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0000403	PMID:15810001	PCS		12/16			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:245150	Keutel syndrome		HP:0004969	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0000400	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0000246	OMIM:245150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:245150	Keutel syndrome		HP:0009778	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0008747	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0006646	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0001611	OMIM:245150	IEA					P	HPO:iea[2009-02-17]
OMIM:245150	Keutel syndrome		HP:0002787	PMID:15810001	PCS					P	HPO:probinson[2023-03-28]
OMIM:208050	Arterial tortuosity syndrome		HP:0001650	PMID:17935213	PCS		7/15			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000483	PMID:17935213	PCS		5/15			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000563	PMID:17935213	PCS		3/14			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001371	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0001252	OMIM:208050	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:208050	Arterial tortuosity syndrome		HP:0002140	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0003593	PMID:17935213	PCS		5/16			C	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001290	OMIM:208050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:208050	Arterial tortuosity syndrome		HP:0012745	PMID:17935213	PCS		9/14			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0011463	PMID:17935213	PCS		1/16			C	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0011462	PMID:17935213	PCS		3/16			C	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000316	PMID:17935213	PCS		6/16			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0002616	PMID:17935213	PCS		2/16			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0004955	PMID:17935213	PCS		15/15			P	HPO:probinson[2012-06-10];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001249	OMIM:208050	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:208050	Arterial tortuosity syndrome		HP:0005328	PMID:17935213	PCS		7/14			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0003623	PMID:17935213	PCS		3/16			C	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0002036	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0000494	PMID:17935213	PCS		8/15			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001382	PMID:17935213	PCS		12/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001977	OMIM:208050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208050	Arterial tortuosity syndrome		HP:0000767	PMID:17935213	PCS		3/15			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001537	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0000007	OMIM:208050	IEA					I	HPO:iea[2009-02-17]
OMIM:208050	Arterial tortuosity syndrome		HP:0001659	OMIM:208050	IEA					P	HPO:iea[2009-02-17]
OMIM:208050	Arterial tortuosity syndrome		HP:0000768	PMID:17935213	PCS		2/15			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000444	PMID:17935213	PCS		8/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000400	PMID:17935213	PCS		7/15			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000963	PMID:17935213	PCS		4/13			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0003577	PMID:17935213;OMIM:208050	PCS		12/26			C	HPO:probinson[2023-01-23];HPO:skoehler[2010-06-19]
OMIM:208050	Arterial tortuosity syndrome		HP:0000343	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0000023	OMIM:208050	IEA		8/15			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000581	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0007421	OMIM:208050	IEA					P	HPO:iea[2009-02-17]
OMIM:208050	Arterial tortuosity syndrome		HP:0000978	OMIM:208050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208050	Arterial tortuosity syndrome		HP:0000218	PMID:17935213	PCS		5/13			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000977	PMID:17935213	PCS		7/15			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001027	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0000776	PMID:17935213	PCS		7/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0004415	PMID:17935213	PCS		5/16			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000974	PMID:17935213	PCS		7/14			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000973	PMID:17935213	PCS		5/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0001166	OMIM:208050	IEA		6/15			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0003621	PMID:17935213	PCS		2/16			C	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0002650	PMID:17935213	PCS		3/15			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000276	PMID:17935213	PCS		14/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000193	PMID:17935213	PCS		0/14			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000272	PMID:17935213	PCS		9/14			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0012158	PMID:17935213	PCS		1/16			P	HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000822	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0001714	OMIM:208050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208050	Arterial tortuosity syndrome		HP:0006687	PMID:17935213	PCS		14/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000347	PMID:17935213	PCS		5/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-23]
OMIM:208050	Arterial tortuosity syndrome		HP:0000545	PMID:17935213	PCS		6/15			P	HPO:probinson[2023-01-23]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0004325	PMID:22052668	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0003577	PMID:22052668	PCS		2/2			C	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0002980	PMID:22052668	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000365	PMID:22052668	PCS		0/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000343	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0004322	PMID:22052668	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0001252	OMIM:614856	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0001290	PMID:22052668	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0010501	PMID:22052668	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000939	PMID:22052668	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0011001	OMIM:614856	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0100625	PMID:22052668	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000337	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000637	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0002757	PMID:22052668	PCS		3/4			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000411	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0001249	PMID:22052668	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0001166	PMID:22052668	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0002751	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0003202	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0003863	PMID:22052668	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0002650	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000233	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0002230	PMID:22052668	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0001382	PMID:22052668	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000592	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0003183	PMID:22052668	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0002194	PMID:22052668	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0003083	OMIM:614856	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0010677	PMID:22052668	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000926	PMID:22052668	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0001537	PMID:22052668	PCS		4/4			P	HPO:probinson[2023-02-22];HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000007	PMID:22052668	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0006387	PMID:22052668	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000703	PMID:22052668	PCS		0/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000527	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000768	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0002645	PMID:22052668	PCS		2/2			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-22]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0000325	PMID:22052668	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:614856	Osteogenesis imperfecta, type XIII		HP:0004349	PMID:22052668	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0000044	PMID:22335740	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0003621	PMID:22335740	PCS		4/4			C	HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0000013	PMID:22335740	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0002750	PMID:22335740	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0030344	PMID:22335740	PCS		4/4			P	HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0030341	PMID:22335740	PCS		4/4			P	HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0000007	PMID:22335740	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0000458	PMID:22335740	PCS		0/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-09-29]
OMIM:614842	Hypogonadotropic hypogonadism 13 with or without anosmia		HP:0008214	PMID:22335740	PCS		4/4			P	HPO:probinson[2022-09-29]
OMIM:176250	Posterior column ataxia		HP:0002650	OMIM:176250	TAS					P	HPO:probinson[2009-02-17]
OMIM:176250	Posterior column ataxia		HP:0002495	OMIM:176250	TAS					P	HPO:probinson[2012-07-16]
OMIM:176250	Posterior column ataxia		HP:0001251	OMIM:176250	TAS					P	HPO:probinson[2009-02-17]
OMIM:176250	Posterior column ataxia		HP:0000006	OMIM:176250	TAS					I	HPO:probinson[2009-02-17]
OMIM:176250	Posterior column ataxia		HP:0001315	OMIM:176250	TAS					P	HPO:probinson[2012-07-16]
OMIM:176250	Posterior column ataxia		HP:0010831	OMIM:176250	TAS					P	HPO:probinson[2012-07-16]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0001891	PMID:35266071;PMID:34326534	PCS		3/4			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0001894	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0002583	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0005231	PMID:34326534	PCS		2/2			P	HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0030374	PMID:35266071	PCS		1/1			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0003593	PMID:35266071	IEA		1/1			C	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0011463	PMID:34326534	IEA		1/3			C	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0012450	PMID:35266071	PCS		1/1			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0001824	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0100827	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0001945	PMID:35266071	PCS		0/1			P	HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0009789	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0040218	PMID:35266071	PCS		1/1			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0001369	PMID:35266071	PCS		1/1			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0003565	PMID:34326534	PCS		2/3			P	HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0002014	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0003621	PMID:34326534	PCS		2/3			C	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0002037	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0000155	PMID:35266071;PMID:34326534	PCS		4/4			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0030783	PMID:35266071	PCS		1/1			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0011227	PMID:34326534	PCS		3/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0100633	PMID:34326534	PCS		1/2			P	HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0001419	PMID:34326534	PCS					I	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0001954	PMID:34326534	PCS		3/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0000988	PMID:35266071	PCS		1/1			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0002205	PMID:35266071	PCS		1/1			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0005218	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:301074	Autoinflammatory syndrome, familial, X-linked, Behcet-like 2		HP:0002027	PMID:34326534	PCS		1/3			P	HPO:probinson[2022-06-13]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0002421	PMID:28132692	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0002188	PMID:28132692	PCS		4/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001250	PMID:28132692	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001252	PMID:28132692	PCS		6/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0002020	PMID:28132692	PCS		1/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0003593	PMID:28132692	PCS		7/7			C	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0012469	PMID:28132692	PCS		4/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0000518	PMID:28132692	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001508	PMID:28132692	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0000737	PMID:28132692	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0000733	PMID:28132692	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0000455	PMID:28132692	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001249	PMID:28132692	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0002059	PMID:28132692	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001344	PMID:28132692	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0002650	PMID:28132692	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0002870	PMID:28132692	PCS		1/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001288	PMID:28132692	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0011968	PMID:28132692	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001263	PMID:28132692	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0005484	PMID:28132692	PCS		5/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0031951	PMID:28132692	PCS		1/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0034392	PMID:28132692	PCS		1/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0032792	PMID:28132692	PCS		2/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0001257	PMID:28132692	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0007359	PMID:28132692	PCS		1/7			P	HPO:probinson[2022-11-01]
OMIM:617393	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination		HP:0000006	PMID:28132692	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001374	PMID:10710233	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000365	OMIM:308050	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000882	OMIM:308050	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0004322	PMID:12668600	PCS		HP:0040283			P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000122	PMID:32819291	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001371	PMID:10710233	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0005650	PMID:33139364	PCS		1/1			P	HPO:probinson[2024-08-06]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000954	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0003826	OMIM:308050	TAS					C	HPO:iea[2009-10-24];HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000835	OMIM:308050	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0002977	OMIM:308050	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0009429	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0008417	PMID:10710233	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0003764	PMID:10710235	PCS		1/2			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0008839	OMIM:308050	PCS		12/20		HP:0012833;HP:0012833	P	HPO:iea[2009-10-26];HPO:probinson[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0004692	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0025092	PMID:10710235	PCS		1/2			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0010760	PMID:10710235	PCS		2/2			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0007431	PMID:12668600	PCS		HP:0040280		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001537	OMIM:308050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0009576	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0006101	PMID:32819291	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0008883	OMIM:308050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000204	OMIM:308050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000126	OMIM:308050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000962	PMID:10710235	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001671	OMIM:308050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0003577	PMID:33139364;PMID:10710235	PCS		3/3			C	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001792	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001036	PMID:33139364;PMID:10710235	PCS		2/3			P	HPO:iea[2009-10-26];HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0002089	PMID:12668600	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001596	PMID:12668600	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001750	OMIM:308050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0005990	OMIM:308050	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0010783	PMID:33139364	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0040162	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0009565	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001423	PMID:10710235	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000894	PMID:10710233	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000773	PMID:10710233	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0010816	PMID:10710235	PCS		1/2			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0002650	PMID:10710233	PCS		HP:0040283			P	HPO:iea[2009-10-26]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0003465	PMID:10710233	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0003462	PMID:10710233	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0005280	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0010655	PMID:12668600	PCS	HP:0003593	HP:0040281		HP:0012833	P	HPO:iea[2012-07-30]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0009438	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0001159	PMID:33139364	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:308050	Congenital hemidysplasia with ichthyosiform erythroderma and limb defects		HP:0000347	OMIM:308050	PCS		HP:0040283		HP:0012833	P	HPO:iea[2009-02-17]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0003422	PMID:16385447	PCS		1/1			P	HPO:probinson[2013-03-30];HPO:probinson[2022-09-25]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0003577	PMID:16385447	PCS		1/1			C	HPO:probinson[2022-09-25]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0004598	PMID:16385447	PCS		1/1			P	HPO:probinson[2013-03-30];HPO:probinson[2022-09-25]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0002650	PMID:16385447	PCS		1/1			P	HPO:probinson[2013-03-30];HPO:probinson[2022-09-25]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0004322	PMID:16385447	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0003311	OMIM:609813	IEA					P	HPO:skoehler[2019-04-18]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0009540	PMID:16385447	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0000902	OMIM:609813	IEA					P	HPO:skoehler[2019-04-18]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0002808	OMIM:609813	IEA					P	HPO:skoehler[2019-04-18]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0000007	PMID:16385447	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-09-25]
OMIM:609813	Spondylocostal dysostosis 3, autosomal recessive		HP:0001238	PMID:16385447	PCS	HP:0003577	1/1			P	HPO:probinson[2013-03-30];HPO:probinson[2022-09-25]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0000154	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0000582	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0004467	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0003057	OMIM:273390	IEA					P	HPO:skoehler[2015-01-27]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0001092	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0008070	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0000968	OMIM:273390	IEA					P	HPO:skoehler[2015-01-14]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0001939	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0001537	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0000007	OMIM:273390	IEA					I	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0000414	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0002705	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0002714	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0000960	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0002019	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0000028	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0001249	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:273390	Tetra-Amelia with ectodermal dysplasia and lacrimal duct abnormalities		HP:0007900	OMIM:273390	IEA					P	HPO:iea[2009-02-17]
OMIM:181800	Scoliosis, idiopathic, susceptibility to, 1		HP:0002650	OMIM:181800	IEA					P	HPO:iea[2009-02-17]
OMIM:181800	Scoliosis, idiopathic, susceptibility to, 1		HP:0000006	OMIM:181800	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:613693	Long QT syndrome 6		HP:0001663	PMID:10219239	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:613693	Long QT syndrome 6		HP:0001695	PMID:10219239	PCS		2/3			P	HPO:probinson[2022-07-09]
OMIM:613693	Long QT syndrome 6		HP:0003581	PMID:10219239	PCS		3/3			C	HPO:probinson[2022-07-09]
OMIM:613693	Long QT syndrome 6		HP:0001657	OMIM:613693	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613693	Long QT syndrome 6		HP:0005184	PMID:10219239	PCS		3/3			P	HPO:probinson[2022-07-09]
OMIM:613693	Long QT syndrome 6		HP:0001279	OMIM:613693	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613693	Long QT syndrome 6		HP:0001664	PMID:10219239	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:613693	Long QT syndrome 6		HP:0001645	OMIM:613693	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613693	Long QT syndrome 6		HP:0000006	PMID:10219239	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:300424	Retinitis pigmentosa 23		HP:0025573	PMID:10892847	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0001133	PMID:10892847	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0003621	PMID:10892847	PCS		1/2			C	HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0000551	PMID:10892847	PCS		1/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0001141	PMID:10892847	PCS		2/2			P	HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0030825	PMID:10892847	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0001419	PMID:22619378	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0011463	PMID:10892847	PCS		1/2			C	HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0000613	PMID:10892847	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0000510	PMID:10892847	PCS		2/2			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0007787	PMID:10892847	PCS		1/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0007722	PMID:10892847	PCS		2/2			P	HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0007843	PMID:10892847	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:300424	Retinitis pigmentosa 23		HP:0025549	PMID:10892847	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:613863	Generalized epilepsy with febrile seizures plus, type 7		HP:0002069	OMIM:613863	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613863	Generalized epilepsy with febrile seizures plus, type 7		HP:0002373	OMIM:613863	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613863	Generalized epilepsy with febrile seizures plus, type 7		HP:0002121	OMIM:613863	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613863	Generalized epilepsy with febrile seizures plus, type 7		HP:0010819	OMIM:613863	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613863	Generalized epilepsy with febrile seizures plus, type 7		HP:0003828	OMIM:613863	TAS					M	HPO:skoehler[2012-10-17]
OMIM:613863	Generalized epilepsy with febrile seizures plus, type 7		HP:0007359	OMIM:613863	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613863	Generalized epilepsy with febrile seizures plus, type 7		HP:0000006	OMIM:613863	TAS					I	HPO:skoehler[2012-10-17]
OMIM:605967	Acropectoral syndrome		HP:0001199	OMIM:605967	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605967	Acropectoral syndrome		HP:0100258	OMIM:605967	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605967	Acropectoral syndrome		HP:0000767	OMIM:605967	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605967	Acropectoral syndrome		HP:0000768	OMIM:605967	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605967	Acropectoral syndrome		HP:0009944	OMIM:605967	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605967	Acropectoral syndrome		HP:0000006	OMIM:605967	TAS					I	HPO:skoehler[2012-10-17]
OMIM:309400	Menkes disease		HP:0001276	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0002421	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0002521	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0003016	OMIM:309400	TAS					P	HPO:probinson[2012-06-10]
OMIM:309400	Menkes disease		HP:0002045	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0001596	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0004322	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0001250	PMID:34430447	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0001010	PMID:34430447	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0001252	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0003593	PMID:34430447	PCS		1/1			C	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0005054	OMIM:309400	TAS					P	HPO:probinson[2012-06-10]
OMIM:309400	Menkes disease		HP:0008070	OMIM:309400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:309400	Menkes disease		HP:0000939	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0001249	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0000973	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0010837	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0000252	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0003487	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0002299	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0002376	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0001382	PMID:34430447	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0002170	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0011097	PMID:34430447	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:309400	Menkes disease		HP:0003819	OMIM:309400	IEA					C	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0001419	OMIM:309400	IEA					I	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0001511	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0002645	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:309400	Menkes disease		HP:0000248	OMIM:309400	IEA					P	HPO:iea[2009-02-17]
OMIM:619396	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10		HP:0012302	PMID:31806906	PCS		5/5			P	HPO:probinson[2021-08-22]
OMIM:619396	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10		HP:0000006	PMID:31806906	PCS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0003676	PMID:30057031	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001310	PMID:30057031	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001332	PMID:30057031	PCS		4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001272	PMID:30057031	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001250	PMID:30057031	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001252	PMID:30057031	PCS					P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001251	PMID:30057031	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0003593	PMID:30057031	PCS		2/7			C	HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0030319	PMID:30057031	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0000639	PMID:30057031	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0011463	PMID:30057031	PCS		3/7			C	HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001249	PMID:30057031	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001347	PMID:30057031	PCS		1/5			P	HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0002059	PMID:30057031	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0002015	PMID:30057031	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0003621	PMID:30057031	PCS		2/7			C	HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001344	PMID:30057031	PCS		5/5			P	HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0003487	PMID:30057031	PCS		1/5			P	HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001266	PMID:30057031	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0002376	PMID:30057031	PCS		5/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001260	PMID:30057031	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001263	PMID:30057031	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0002371	PMID:30057031	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0007371	PMID:30057031	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0002505	PMID:30057031	PCS		6/7			P	HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0000565	PMID:30057031	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0002403	PMID:30057031	PCS		1/5			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0001257	PMID:30057031	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:618088	Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures		HP:0000006	PMID:30057031	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0003621	PMID:33465056	PCS		10/28			C	HPO:probinson[2022-08-27]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0011463	PMID:33465056	PCS		1/28			C	HPO:probinson[2022-08-27]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0011462	PMID:33465056	PCS		17/28			C	HPO:probinson[2022-08-27]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0020120	PMID:33465056	PCS					P	HPO:probinson[2021-07-16];HPO:probinson[2021-07-16]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0000007	PMID:33465056	PCS					I	HPO:probinson[2021-07-16];HPO:probinson[2022-08-27]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0007663	PMID:33465056	PCS					P	HPO:probinson[2021-07-16];HPO:probinson[2021-07-16]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0007763	PMID:33465056	PCS					P	HPO:probinson[2021-07-16];HPO:probinson[2021-07-16]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0000603	PMID:33465056	PCS		24/29			P	HPO:probinson[2021-07-16]
OMIM:619382	Leber hereditary optic neuropathy, autosomal recessive		HP:0007768	PMID:33465056	PCS					P	HPO:probinson[2021-07-16];HPO:probinson[2021-07-16]
OMIM:240000	Hyperuricemia, infantile, with abnormal behavior and normal hypoxanthineguanine phosphoribosyltransferase		HP:0000164	OMIM:240000	TAS					P	HPO:skoehler[2013-02-25]
OMIM:240000	Hyperuricemia, infantile, with abnormal behavior and normal hypoxanthineguanine phosphoribosyltransferase		HP:0001344	OMIM:240000	TAS					P	HPO:probinson[2009-02-17]
OMIM:240000	Hyperuricemia, infantile, with abnormal behavior and normal hypoxanthineguanine phosphoribosyltransferase		HP:0000717	OMIM:240000	TAS					P	HPO:skoehler[2013-02-25]
OMIM:240000	Hyperuricemia, infantile, with abnormal behavior and normal hypoxanthineguanine phosphoribosyltransferase		HP:0000007	OMIM:240000	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:240000	Hyperuricemia, infantile, with abnormal behavior and normal hypoxanthineguanine phosphoribosyltransferase		HP:0001249	OMIM:240000	TAS					P	HPO:probinson[2009-02-17]
OMIM:240000	Hyperuricemia, infantile, with abnormal behavior and normal hypoxanthineguanine phosphoribosyltransferase		HP:0000522	OMIM:240000	TAS					P	HPO:probinson[2009-02-17]
OMIM:240000	Hyperuricemia, infantile, with abnormal behavior and normal hypoxanthineguanine phosphoribosyltransferase		HP:0002149	OMIM:240000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0001397	PMID:21345103	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0001297	PMID:21345103	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0002155	PMID:21345103	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0005268	PMID:21345103	PCS		1/3			C	HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0100578	PMID:21345103	PCS		3/3			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0011462	PMID:21345103	PCS		3/3			C	HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0000855	PMID:21345103	PCS		3/3			P	HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0000822	PMID:21345103	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0000876	PMID:21345103	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0009125	PMID:21345103	PCS		3/3			P	HPO:probinson[2022-04-01];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0000956	PMID:21345103	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0003712	PMID:21345103	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0000831	PMID:21345103	PCS		2/3			P	HPO:probinson[2022-04-01]
OMIM:613877	Lipodystrophy, familial partial, type 4		HP:0000006	PMID:21345103	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-01]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0002421	PMID:17187373	PCS		7/7			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0003577	PMID:17187373;PMID:15236405;PMID:10508519	PCS		10/10			C	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0003324	PMID:15236405;PMID:10508519	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0002015	PMID:17187373	PCS		6/7			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0001662	PMID:17187373	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0011968	PMID:17187373;PMID:10508519	PCS		9/9			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0001252	PMID:15236405;PMID:10508519	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0001290	PMID:17187373	PCS		7/7			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0002093	PMID:10508519	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0030319	PMID:17187373	PCS		14/14			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0100297	PMID:15236405	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0008180	PMID:17187373	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0003819	PMID:17187373	PCS		1/7			C	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0000007	PMID:10508519	PCS					I	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0025336	PMID:17187373	PCS		7/7			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0003811	PMID:10508519	PCS		2/2			C	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0001522	PMID:17187373	PCS		4/7			C	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0003798	PMID:15236405;PMID:10508519	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0003557	PMID:15236405	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620265	Congenital myopathy 2B, severe infantile, autosomal recessive		HP:0004887	PMID:15236405	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0000365	PMID:32286009	PCS		2/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0004322	PMID:32286009	PCS		5/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0001250	PMID:32286009	PCS	HP:0003593	11/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0001272	PMID:32286009	PCS		4/10		HP:0012825	P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0012706	PMID:32286009	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0012708	PMID:32286009	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0410170	PMID:32286009	PCS		2/9			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0100502	PMID:32286009	PCS		3/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0011182	PMID:32286009	PCS		7/8			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0001508	PMID:32286009	PCS		6/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002719	PMID:32286009	PCS		6/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0100704	PMID:32286009	PCS		3/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0009125	PMID:32286009	PCS		2/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0003429	PMID:32286009	PCS		8/10			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002835	PMID:32286009	PCS					P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0001522	PMID:32286009	PCS		4/11			C	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0001249	PMID:32286009	PCS		11/11			P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0001347	PMID:32286009	PCS		4/6			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0008936	PMID:32286009	PCS		8/8			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0001561	PMID:32286009	PCS	HP:0030674	4/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0000252	PMID:32286009	PCS		8/8			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002015	PMID:32286009	PCS		4/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002059	PMID:32286009	PCS		8/10			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002133	PMID:32286009	PCS		4/8			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0000871	PMID:32286009	PCS		1/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002079	PMID:32286009	PCS		7/8			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0011344	PMID:32286009	PCS		11/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0011470	PMID:32286009	PCS		1/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002509	PMID:32286009	PCS		7/8			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0000007	PMID:32286009	PCS					I	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0000821	PMID:32286009	PCS		1/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0000824	PMID:32286009	PCS		1/11			P	HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0002643	PMID:32286009	PCS	HP:0003623	5/11			P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618922	Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities		HP:0000742	PMID:32286009	PCS		1/11			P	HPO:probinson[2020-08-31]
OMIM:607631	Epilepsy, juvenile absence		HP:0010849	PMID:17159113	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:607631	Epilepsy, juvenile absence		HP:0007193	PMID:17159113	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-19]
OMIM:607631	Epilepsy, juvenile absence		HP:0003621	PMID:17159113	PCS		2/2			C	HPO:probinson[2022-08-19]
OMIM:607631	Epilepsy, juvenile absence		HP:0002123	OMIM:607631	IEA					P	HPO:iea[2009-02-17]
OMIM:607631	Epilepsy, juvenile absence		HP:0002121	PMID:17159113	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:607631	Epilepsy, juvenile absence		HP:0000006	PMID:17159113	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000044	PMID:28067909	PCS		17/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000023	OMIM:603457	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0410030	PMID:28067909	PCS		2/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000518	PMID:28067909	PCS		9/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000316	OMIM:603457	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000458	PMID:28067909	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000218	PMID:28067909	PCS		27/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000059	OMIM:603457	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000377	PMID:28067909	PCS		1/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000413	PMID:28067909	PCS		2/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0001249	PMID:28067909	PCS		9/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000175	PMID:28067909	PCS		6/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000054	PMID:28067909	PCS			MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000453	OMIM:603457	TAS					P	HPO:skoehler[2015-01-21]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0009927	PMID:28067909	PCS	HP:0003577				P	HPO:skoehler[2015-01-21];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0011800	PMID:28067909	PCS		22/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0011268	PMID:28067909	PCS		1/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000689	PMID:28067909	PCS		3/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000568	OMIM:603457	TAS					P	HPO:skoehler[2015-01-21];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0006784	PMID:28067909	PCS		12/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000405	PMID:28067909	PCS		2/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000664	OMIM:603457	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000685	PMID:28067909	PCS		9/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000047	OMIM:603457	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000564	PMID:28067909	PCS		24/40			P	HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000006	PMID:28067909	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000589	PMID:28067909	PCS		19/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000028	PMID:28067909	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:603457	Bosma arhinia microphthalmia syndrome		HP:0000786	PMID:28067909	PCS			FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000044	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0002444	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0003577	PMID:15812812	PCS		9/9			C	HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0010627	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0004322	PMID:15812812	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001252	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001274	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001290	OMIM:206900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:206900	Microphthalmia, syndromic 3		HP:0012521	PMID:16145681	PCS		1/1			P	HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001629	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000518	PMID:15812812	PCS		1/9			P	HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0002937	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001328	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0008897	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001643	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0008417	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0002510	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001264	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000054	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000252	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0008619	PMID:16145681	PCS		1/1			P	HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0002079	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0002032	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0001263	PMID:16145681	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000609	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000407	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000902	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000528	PMID:16145681;PMID:15812812	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-24];HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0002948	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000921	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000568	PMID:15812812	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0005815	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000647	PMID:15812812	PCS		2/9			P	HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0002007	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0003316	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000047	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000028	OMIM:206900	IEA					P	HPO:iea[2009-02-17]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000589	PMID:15812812	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-24]
OMIM:206900	Microphthalmia, syndromic 3		HP:0000006	OMIM:206900	IEA					I	HPO:iea[2009-02-17]
OMIM:615235	Cardiomyopathy, dilated, 1JJ		HP:0003596	PMID:17646580	PCS		1/3			C	HPO:probinson[2022-07-03]
OMIM:615235	Cardiomyopathy, dilated, 1JJ		HP:0003584	PMID:17646580	PCS		1/3			C	HPO:probinson[2022-07-03]
OMIM:615235	Cardiomyopathy, dilated, 1JJ		HP:0011462	PMID:17646580	PCS		1/3			C	HPO:probinson[2022-07-03]
OMIM:615235	Cardiomyopathy, dilated, 1JJ		HP:0012664	PMID:17646580	PCS		3/3			P	HPO:probinson[2022-07-03]
OMIM:615235	Cardiomyopathy, dilated, 1JJ		HP:0000006	PMID:17646580	PCS					I	HPO:skoehler[2013-06-04];HPO:probinson[2022-07-03]
OMIM:615235	Cardiomyopathy, dilated, 1JJ		HP:0001644	PMID:17646580	PCS		3/3		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-07-03]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0000252	PMID:24031089	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0003577	PMID:24031089	PCS		8/8			C	HPO:probinson[2022-07-11]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0002650	PMID:24031089	PCS		1/8			P	HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0100490	PMID:24031089	PCS	HP:0003577	8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0008807	PMID:24031089	PCS	HP:0003577	8/8			P	HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0002121	PMID:24031089	PCS		2/8			P	HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0001263	PMID:24031089	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0001290	PMID:24031089	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0000308	PMID:24031089	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0000729	PMID:24031089	PCS		8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0002827	PMID:24031089	PCS	HP:0003577	8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0011461	PMID:24031089	PCS		8/8			C	HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0011153	PMID:24031089	PCS		4/8			P	HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0002804	PMID:24031089	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0000007	PMID:24031089	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0001249	PMID:24031089	PCS		5/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:615553	Arthrogryposis, impaired intellectual development, and seizures		HP:0004976	PMID:24031089	PCS		8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-26]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003431	PMID:10848494	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003376	PMID:10848494	PCS					P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003693	PMID:10848494	PCS					P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0002066	PMID:10848494	PCS					P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0002460	PMID:10848494	PCS					P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003690	OMIM:614895	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0001270	OMIM:614895	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0002280	PMID:10848494	PCS		2/2			P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0011463	PMID:10848494	PCS					C	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0002936	PMID:10848494	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0001604	OMIM:614895	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0008954	PMID:10848494	PCS					P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003400	OMIM:614895	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003202	OMIM:614895	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0002136	PMID:10848494	PCS					P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003387	OMIM:614895	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0002650	PMID:10848494	PCS		8/8			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0001288	PMID:10848494	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0001761	PMID:10848494	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003383	PMID:10848494	PCS		1/1			P	HPO:probinson[2022-11-04];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0001284	PMID:10848494	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003380	PMID:10848494	PCS					P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0010871	PMID:10848494	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0011096	PMID:10848494	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0000007	PMID:11157804	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0002505	PMID:10848494	PCS	HP:0003581	1/8			P	HPO:probinson[2022-11-04]
OMIM:614895	Charcot-Marie-Tooth disease, demyelinating, type 4F		HP:0003677	PMID:10848494	PCS					C	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-04]
OMIM:613122	Cardiomyopathy, dilated, 1cc		HP:0003596	PMID:19881492	PCS		7/9			C	HPO:probinson[2022-07-03]
OMIM:613122	Cardiomyopathy, dilated, 1cc		HP:0003584	PMID:19881492	PCS		1/9			C	HPO:probinson[2022-07-03]
OMIM:613122	Cardiomyopathy, dilated, 1cc		HP:0011462	PMID:19881492	PCS		1/9			C	HPO:probinson[2022-07-03]
OMIM:613122	Cardiomyopathy, dilated, 1cc		HP:0012664	PMID:19881492	PCS		7/7			P	HPO:probinson[2022-07-03]
OMIM:613122	Cardiomyopathy, dilated, 1cc		HP:0033755	PMID:19881492	PCS		8/8			P	HPO:probinson[2022-07-03]
OMIM:613122	Cardiomyopathy, dilated, 1cc		HP:0000006	PMID:19881492	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-03]
OMIM:613122	Cardiomyopathy, dilated, 1cc		HP:0001644	PMID:19881492	PCS	HP:0003581	9/9			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-07-03]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0003477	PMID:20074521	PCS		4/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0010628	PMID:20074521	PCS		3/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0030303	PMID:20074521	PCS		7/8			P	HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0002079	PMID:20074521	PCS		6/7			P	HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0100490	OMIM:600638	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0001491	PMID:20074521	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0001274	OMIM:600638	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0001263	PMID:20074521	PCS		4/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0025102	PMID:20074521	PCS		4/7			P	HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0012242	OMIM:600638	TAS					P	HPO:skoehler[2014-11-26]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0009473	OMIM:600638	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0012241	OMIM:600638	TAS					P	HPO:skoehler[2013-04-18]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0000508	OMIM:600638	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0000646	OMIM:600638	IEA					P	HPO:iea[2009-02-17]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0001328	OMIM:600638	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0001239	OMIM:600638	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0007831	OMIM:600638	IEA					P	HPO:iea[2009-02-17]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0001477	OMIM:600638	IEA					P	HPO:iea[2009-02-17]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0000006	PMID:20074521	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:600638	Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement		HP:0000577	OMIM:600638	IEA					P	HPO:iea[2009-02-17]
OMIM:618077	Inflammatory bowel disease 29		HP:0100279	PMID:21983784	PCS					P	HPO:probinson[2020-05-15]
OMIM:618077	Inflammatory bowel disease 29		HP:0100280	PMID:21983784	PCS					P	HPO:probinson[2020-05-15]
OMIM:618077	Inflammatory bowel disease 29		HP:0003829	PMID:21983784	PCS					I	HPO:probinson[2020-05-15]
OMIM:618077	Inflammatory bowel disease 29		HP:0000006	PMID:21983784	TAS					I	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:608264	Deafness, congenital neurosensory, autosomal recessive 40		HP:0000007	OMIM:608264	TAS					I	HPO:probinson[2009-02-17]
OMIM:608264	Deafness, congenital neurosensory, autosomal recessive 40		HP:0000399	OMIM:608264	TAS				HP:0012829	P	HPO:probinson[2009-02-17]
OMIM:619369	Lymphatic malformation 10		HP:0000034	PMID:32908006	PCS		4/5	MALE		P	HPO:probinson[2021-07-10]
OMIM:619369	Lymphatic malformation 10		HP:0003593	PMID:32908006	PCS		6/7			C	HPO:probinson[2021-07-10]
OMIM:619369	Lymphatic malformation 10		HP:0001004	PMID:32908006	PCS		7/7			P	HPO:probinson[2021-07-10]
OMIM:619369	Lymphatic malformation 10		HP:0000006	PMID:32908006	PCS					I	HPO:probinson[2021-07-10];HPO:probinson[2021-07-10]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0001696	PMID:29727692	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0001651	PMID:29727692	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0002110	OMIM:618063	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0033036	PMID:29727692	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0031245	PMID:29727692	PCS		3/3			P	HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0011109	OMIM:618063	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0012259	PMID:29727692	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0012384	OMIM:618063	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0012263	PMID:29727692	PCS		3/3			P	HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0000789	OMIM:618063	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0000007	PMID:29727692	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0000405	OMIM:618063	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0000389	OMIM:618063	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0002643	PMID:29727692	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:618063	Ciliary dyskinesia, primary, 38		HP:0003623	PMID:29727692	PCS		3/3			C	HPO:probinson[2023-02-18]
OMIM:306900	Hemophilia B		HP:0005542	OMIM:306900	IEA					P	HPO:iea[2009-02-17]
OMIM:306900	Hemophilia B		HP:0011858	PMID:34017743	PCS		31/31			P	HPO:probinson[2012-08-01];HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0000790	PMID:34017743	PCS		2/31			P	HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0005261	PMID:34017743	PCS		25/31			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0008151	PMID:34017743	PCS		0/31			P	HPO:probinson[2012-08-01];HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0001419	OMIM:306900	TAS					I	HPO:probinson[2009-02-17]
OMIM:306900	Hemophilia B		HP:0000967	PMID:34017743	PCS		2/31			P	HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0000978	PMID:34017743	PCS		29/31			P	HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0002758	OMIM:306900	IEA					P	HPO:iea[2009-02-17]
OMIM:306900	Hemophilia B		HP:0001934	PMID:34017743	PCS		27/31			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0002249	PMID:34017743	PCS		4/31			P	HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0002239	OMIM:306900	IEA					P	HPO:iea[2009-02-17]
OMIM:306900	Hemophilia B		HP:0000421	PMID:34017743	PCS		7/31			P	HPO:probinson[2024-03-09]
OMIM:306900	Hemophilia B		HP:0003645	OMIM:306900	TAS					P	HPO:probinson[2009-02-17]
OMIM:306900	Hemophilia B		HP:0002248	PMID:34017743	PCS		4/31			P	HPO:probinson[2024-03-09]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0002069	PMID:19710327	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0006813	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0002123	PMID:19710327	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0002373	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0001250	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0001263	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0003593	PMID:19710327	PCS		1/1			C	HPO:probinson[2023-02-26]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0001290	PMID:19710327	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0002070	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0007270	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0007281	OMIM:617350	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0003819	PMID:19710327	PCS		1/1			C	HPO:probinson[2023-02-26]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0000007	PMID:19710327	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0007256	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0200134	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617350	Epileptic encephalopathy, early infantile, 52		HP:0001257	OMIM:617350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000286	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001254	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000046	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001252	PMID:12217961	PCS		1/1			P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0003593	PMID:12217961	PCS		1/1			C	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001290	PMID:11983712	PCS		1/1			P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0020045	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001643	OMIM:607143	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0004315	PMID:11983712;PMID:12217961	PCS		2/2			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0003623	PMID:11983712	PCS		1/1			C	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000253	PMID:11983712	PCS		1/1			P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0003642	PMID:11983712;PMID:12217961	PCS		2/2			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000054	PMID:12217961	PCS		1/1	MALE		P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0011968	PMID:11983712;PMID:12217961	PCS		2/2			P	HPO:probinson[2017-06-24];HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0002033	PMID:11983712	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001263	PMID:11983712;PMID:12217961	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:skoehler[2018-10-08];HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0011800	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000969	OMIM:607143	IEA					P	HPO:skoehler[2019-09-07]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000407	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000007	PMID:11983712	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001976	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0002901	PMID:11983712	PCS		1/1			P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0003316	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0002788	PMID:11983712	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001852	PMID:12217961	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000047	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000322	PMID:12093361	PCS					P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0005736	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0002984	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000325	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001655	OMIM:607143	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000445	OMIM:607143	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000541	OMIM:607143	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0008905	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0003097	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0005792	OMIM:607143	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001508	PMID:11983712	PCS		1/1			P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001943	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000219	OMIM:607143	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0006532	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000377	PMID:12093361	PCS					P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000773	OMIM:607143	IEA					P	HPO:skoehler[2019-09-07]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0003645	PMID:12093361	PCS					P	HPO:probinson[2017-06-24]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0002850	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001561	OMIM:607143	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001762	PMID:12217961	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0002098	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0003186	PMID:12217961	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0001518	OMIM:607143	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0000028	PMID:12217961	PCS		1/1	MALE		P	HPO:skoehler[2019-04-18]
OMIM:607143	Congenital disorder of glycosylation, type Ig		HP:0002720	PMID:12217961	PCS		1/1			P	HPO:probinson[2023-04-10]
OMIM:611721	Combined saposin deficiency		HP:0002487	PMID:1371116	PCS		2/2			P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-21]
OMIM:611721	Combined saposin deficiency		HP:0003577	OMIM:611721	PCS					C	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0003487	OMIM:611721	PCS					P	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0002079	OMIM:611721	PCS					P	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0004343	OMIM:611721	PCS					P	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0011968	OMIM:611721	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611721	Combined saposin deficiency		HP:0001252	OMIM:611721	TAS					P	HPO:skoehler[2014-11-26]
OMIM:611721	Combined saposin deficiency		HP:0002240	PMID:1371116	PCS		2/2			P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-21]
OMIM:611721	Combined saposin deficiency		HP:0002380	OMIM:611721	PCS					P	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0011169	OMIM:611721	PCS					P	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0002518	OMIM:611721	PCS					P	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0000007	PMID:1371116	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2023-02-21]
OMIM:611721	Combined saposin deficiency		HP:0002529	OMIM:611721	PCS					P	HPO:probinson[2009-02-17]
OMIM:611721	Combined saposin deficiency		HP:0000648	OMIM:611721	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611721	Combined saposin deficiency		HP:0001522	PMID:1371116	PCS		2/2			C	HPO:probinson[2012-04-11];HPO:probinson[2023-02-21]
OMIM:611721	Combined saposin deficiency		HP:0007305	OMIM:611721	PCS					P	HPO:probinson[2012-04-11]
OMIM:611721	Combined saposin deficiency		HP:0001744	PMID:1371116	PCS		2/2			P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-21]
OMIM:611721	Combined saposin deficiency		HP:0001336	PMID:1371116	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:611721	Combined saposin deficiency		HP:0003623	PMID:1371116	PCS		2/2			C	HPO:probinson[2023-02-21]
OMIM:146350	Hypophosphatemic bone disease		HP:0002652	OMIM:146350	IEA					P	HPO:iea[2009-02-17]
OMIM:146350	Hypophosphatemic bone disease		HP:0004322	OMIM:146350	IEA					P	HPO:iea[2009-02-17]
OMIM:146350	Hypophosphatemic bone disease		HP:0002748	OMIM:146350	IEA		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:146350	Hypophosphatemic bone disease		HP:0002979	OMIM:146350	IEA					P	HPO:iea[2009-02-17]
OMIM:146350	Hypophosphatemic bone disease		HP:0002749	OMIM:146350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:146350	Hypophosphatemic bone disease		HP:0000006	OMIM:146350	IEA					I	HPO:iea[2009-02-17]
OMIM:146350	Hypophosphatemic bone disease		HP:0002148	OMIM:146350	IEA					P	HPO:iea[2009-02-17]
OMIM:615547	Schaaf-Yang syndrome		HP:0000288	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0001531	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0002540	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0001773	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0004322	PMID:24076603	PCS		2/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0001371	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0001250	OMIM:615547	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0002020	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0003593	OMIM:615547	TAS					C	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0012745	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0004283	PMID:24076603	PCS		1/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000280	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0002019	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0000278	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0001249	PMID:24076603	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0003623	PMID:24076603	PCS		1/4			C	HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000054	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0001344	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0000574	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0011968	PMID:24076603	PCS		3/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0002033	PMID:24076603	PCS		3/4			P	HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0001263	PMID:24076603	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0002591	OMIM:615547;PMID:24076603	PCS		12/14			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0001182	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0012385	PMID:24076603	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000729	PMID:24076603	PCS		4/4			P	HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000565	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0000006	PMID:24076603	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000369	OMIM:615547	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615547	Schaaf-Yang syndrome		HP:0001612	PMID:24076603	PCS		3/4			P	HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000341	PMID:24076603	PCS		1/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0003577	PMID:24076603	PCS		3/4			C	HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0001156	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0030084	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0001989	OMIM:615547	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0000135	PMID:24076603	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000750	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0002650	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0031936	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0000194	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0010535	PMID:24076603	PCS		2/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0100710	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0012166	PMID:24076603	PCS		2/4			P	HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0001838	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0002808	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0002804	OMIM:615547	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0001558	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0001319	PMID:24076603	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0002007	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0200055	PMID:24076603	PCS		1/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000028	PMID:24076603	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-30]
OMIM:615547	Schaaf-Yang syndrome		HP:0000303	OMIM:615547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615547	Schaaf-Yang syndrome		HP:0000545	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615547	Schaaf-Yang syndrome		HP:0001513	OMIM:615547	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0001288	PMID:22522442	PCS		3/3			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0001761	PMID:22522442	PCS		1/3			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0001618	PMID:22522442	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0011462	PMID:22522442	PCS		3/3			C	HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0001284	PMID:22522442	PCS		3/3			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0002460	PMID:22522442	PCS		3/3			P	HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0009027	PMID:22522442	PCS		3/3			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0000007	PMID:22522442	PCS					I	HPO:skoehler[2012-11-25];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0002936	PMID:22522442	PCS		0/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0007269	PMID:22522442	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0003677	PMID:22522442	PCS					C	HPO:skoehler[2012-11-25];HPO:probinson[2023-01-30]
OMIM:614881	Spinal muscular atrophy, distal, autosomal recessive, 5		HP:0008944	PMID:22522442	PCS		3/3			P	HPO:probinson[2023-01-30]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002188	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000486	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002144	PMID:26656649	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000463	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0004322	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0003396	PMID:26656649	PCS		1/1			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000041	PMID:26656649	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0001290	OMIM:616728	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0001270	OMIM:616728	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0012430	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0011220	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000657	PMID:26656649	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0001800	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000219	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002714	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0006895	PMID:26656649	PCS					P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002019	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000256	PMID:26656649	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002558	OMIM:616728	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0003468	PMID:26656649	PCS					P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000577	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002553	OMIM:616728	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000494	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000750	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000431	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002079	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0011968	PMID:26656649	PCS		1/2			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0001382	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000592	PMID:26656649	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0001263	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0001182	OMIM:616728	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000508	PMID:26656649	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0004209	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000664	OMIM:616728	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0002007	OMIM:616728	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0009778	OMIM:616728	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000006	PMID:26656649	PCS					I	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000248	PMID:26656649	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000028	PMID:26656649	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616728	Cleft palate, psychomotor retardation, and distinctive facial features		HP:0000687	PMID:26656649	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:610359	Retinitis pigmentosa 33		HP:0007737	PMID:19878916	PCS					P	HPO:probinson[2013-04-01]
OMIM:610359	Retinitis pigmentosa 33		HP:0000662	PMID:19878916	PCS					P	HPO:probinson[2013-04-01]
OMIM:610359	Retinitis pigmentosa 33		HP:0000505	PMID:19878916	PCS					P	HPO:probinson[2013-04-01]
OMIM:610359	Retinitis pigmentosa 33		HP:0000543	PMID:19878916	PCS					P	HPO:probinson[2013-04-01]
OMIM:610359	Retinitis pigmentosa 33		HP:0000510	OMIM:610359	IEA					P	HPO:skoehler[2015-01-27]
OMIM:610359	Retinitis pigmentosa 33		HP:0007843	PMID:19878916	PCS					P	HPO:probinson[2013-04-01]
OMIM:610359	Retinitis pigmentosa 33		HP:0007722	PMID:19878916	PCS					P	HPO:probinson[2013-04-01]
OMIM:610359	Retinitis pigmentosa 33		HP:0000006	PMID:19878916	PCS					I	HPO:probinson[2013-01-09]
OMIM:608516	Major depressive disorder		HP:0000716	OMIM:608516	TAS					P	HPO:probinson[2022-08-17]
OMIM:608516	Major depressive disorder		HP:0010982	OMIM:608516	TAS					I	HPO:probinson[2022-08-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0003651	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001332	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001250	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001791	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001791	PMID:11567215	PCS	HP:0011461	1/8			P	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0001252	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001251	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0002240	PMID:11567215	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0002185	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0011463	PMID:11567215	PCS		2/8			C	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0000733	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0002878	OMIM:607625	TAS					P	HPO:skoehler[2014-06-24]
OMIM:607625	Niemann-pick disease, type C2		HP:0003349	PMID:11567215	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0001522	PMID:11567215	PCS		4/8			C	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0001249	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0006579	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001744	PMID:11567215	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0000952	PMID:11567215	PCS		5/8			P	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0000511	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0003623	PMID:11567215	PCS		6/8			C	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0002015	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001561	PMID:11567215	PCS		1/8			P	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0003640	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001982	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0004333	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0030223	OMIM:607625	TAS					P	HPO:skoehler[2015-01-20]
OMIM:607625	Niemann-pick disease, type C2		HP:0001260	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001263	PMID:11567215	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0002371	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0002093	PMID:11567215	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0000709	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0003819	PMID:11567215	PCS		2/8			C	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0000726	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0000007	PMID:11567215	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0002524	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0001257	OMIM:607625	IEA					P	HPO:iea[2009-02-17]
OMIM:607625	Niemann-pick disease, type C2		HP:0002206	PMID:11567215	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:607625	Niemann-pick disease, type C2		HP:0002643	PMID:11567215	PCS	HP:0003623	1/8			P	HPO:probinson[2022-09-02]
OMIM:613678	Brachyolmia type 2		HP:0004322	OMIM:613678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613678	Brachyolmia type 2		HP:0000926	OMIM:613678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613678	Brachyolmia type 2		HP:0000007	OMIM:613678	TAS					I	HPO:skoehler[2012-10-17]
OMIM:191420	Ulna metaphyseal dysplasia syndrome		HP:0002673	OMIM:191420	IEA					P	HPO:iea[2009-02-17]
OMIM:191420	Ulna metaphyseal dysplasia syndrome		HP:0002750	OMIM:191420	IEA					P	HPO:iea[2009-02-17]
OMIM:191420	Ulna metaphyseal dysplasia syndrome		HP:0000925	OMIM:191420	IEA					P	HPO:iea[2009-02-17]
OMIM:191420	Ulna metaphyseal dysplasia syndrome		HP:0003072	OMIM:191420	TAS					P	HPO:probinson[2009-02-17]
OMIM:191420	Ulna metaphyseal dysplasia syndrome		HP:0030836	OMIM:191420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:191420	Ulna metaphyseal dysplasia syndrome		HP:0000006	OMIM:191420	IEA					I	HPO:iea[2009-02-17]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:4000148	PMID:29357359	PCS		1/2			P	HPO:probinson[2023-01-27]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0001541	PMID:29357359	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0011461	PMID:29357359	PCS		2/2			C	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0002240	PMID:29357359	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0000007	PMID:29357359	PCS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0001723	PMID:29357359	PCS	HP:0011461	2/2			P	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0001789	PMID:29357359	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0010444	PMID:29357359	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0001522	PMID:29357359	PCS		2/2			C	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0034548	PMID:29357359	PCS		1/2			P	HPO:probinson[2023-03-31]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0001642	PMID:29357359	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619433	Cardiomyopathy, familial restrictive, 6		HP:0005180	PMID:29357359	PCS		2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:609620	Short QT syndrome 1		HP:0012232	PMID:14676148	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-21]
OMIM:609620	Short QT syndrome 1		HP:0001695	PMID:14676148	PCS					P	HPO:probinson[2013-03-31];HPO:probinson[2020-07-21]
OMIM:609620	Short QT syndrome 1		HP:0001962	PMID:12925462	PCS					P	HPO:probinson[2013-03-31];HPO:probinson[2020-07-21]
OMIM:609620	Short QT syndrome 1		HP:0001279	PMID:12925462	PCS					P	HPO:probinson[2013-03-31];HPO:probinson[2020-07-21]
OMIM:609620	Short QT syndrome 1		HP:0004757	PMID:14676148	PCS					P	HPO:probinson[2020-07-21]
OMIM:609620	Short QT syndrome 1		HP:0000006	PMID:14676148	PCS					I	HPO:probinson[2013-03-31];HPO:probinson[2020-07-21]
OMIM:609620	Short QT syndrome 1		HP:0001645	PMID:14676148	PCS					P	HPO:probinson[2020-07-21]
OMIM:308905	Leber optic atrophy, susceptibility to		HP:0001112	OMIM:308905	IEA					P	HPO:skoehler[2015-12-30]
OMIM:308905	Leber optic atrophy, susceptibility to		HP:0000648	OMIM:308905	IEA					P	HPO:skoehler[2010-06-20]
OMIM:308905	Leber optic atrophy, susceptibility to		HP:0001417	OMIM:308905	IEA					I	HPO:iea[2009-02-17]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0001298	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003236	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0001399	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003256	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0012707	PMID:33169484	PCS		1/1			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0033444	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0033465	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0002181	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0012704	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0012444	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0012402	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0002919	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0012470	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0011461	PMID:33169484	PCS		1/2			C	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0001943	PMID:33169484	PCS	HP:0003623	2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0008872	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0008358	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0002119	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0001522	PMID:33169484	PCS		2/2			C	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0002910	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003348	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003623	PMID:33169484	PCS		1/2			C	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0002353	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003542	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0008160	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0000007	PMID:33169484	PCS					I	HPO:probinson[2021-06-21];HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0001635	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0001712	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0008347	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003219	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003217	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0001511	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0004900	PMID:33169484	PCS		2/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0008527	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:619355	Mitochondrial complex IV deficiency, nuclear type 22		HP:0003215	PMID:33169484	PCS		1/2			P	HPO:probinson[2021-06-21]
OMIM:143200	Wagner vitreoretinopathy		HP:0000572	OMIM:143200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:143200	Wagner vitreoretinopathy		HP:0001123	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0030663	PMID:18309337	TAS					P	HPO:skoehler[2015-12-30]
OMIM:143200	Wagner vitreoretinopathy		HP:0000518	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0007773	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0000648	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0007643	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0030490	OMIM:143200	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:143200	Wagner vitreoretinopathy		HP:0007722	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0000006	OMIM:143200	IEA					I	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0000501	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:143200	Wagner vitreoretinopathy		HP:0000545	OMIM:143200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:143200	Wagner vitreoretinopathy		HP:0000533	OMIM:143200	IEA					P	HPO:iea[2009-02-17]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000252	PMID:19914906	PCS		6/10			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000750	PMID:19914906	PCS		10/10			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0004322	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0001250	PMID:19755429;PMID:19914906	PCS		4/13			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000490	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0001270	PMID:19914906	PCS		6/10			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0045075	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0012368	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000319	PMID:19755429	PCS		2/3			P	HPO:probinson[2024-12-27];HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000717	PMID:19755429;PMID:19914906	PCS		3/13			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0008551	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000316	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000219	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0002007	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000653	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0001466	PMID:19914906	PCS					I	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0001249	PMID:19914906	PCS		10/10			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000776	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0001238	PMID:19755429	PCS		1/3			P	HPO:probinson[2024-12-27]
OMIM:614671	Chromosome 16p11.2 duplication syndrome		HP:0000006	PMID:19914906	PCS					I	HPO:probinson[2024-12-27]
OMIM:270100	Heterotaxy, visceral, 5		HP:0003577	PMID:19064609	PCS		14/14			C	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001750	PMID:19064609	PCS		7/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001651	PMID:19064609	PCS		5/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0000089	PMID:9354794	PCS		1/35			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001272	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0011699	PMID:19064609	PCS		2/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0011555	PMID:19064609	PCS		3/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0031565	PMID:9354794	PCS		17/35			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0010305	PMID:9354794	PCS		2/35			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0031348	PMID:19064609	PCS		10/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0011536	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001629	PMID:19064609	PCS		5/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001746	PMID:19064609	PCS		4/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0006695	PMID:19064609	PCS		2/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0004935	PMID:19064609	PCS		8/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001643	PMID:19064609	PCS		4/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0002059	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001321	PMID:9354794	PCS		1/35			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0003363	PMID:9354794	PCS	HP:0003577	3/18	FEMALE		P	HPO:iea[2009-02-17];HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0003363	PMID:19064609	PCS		5/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0000073	PMID:9354794	PCS		1/35			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0004970	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001680	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0000071	PMID:9354794	PCS		1/35			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0010773	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0005160	PMID:19064609	PCS		3/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0011861	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001719	PMID:19064609	PCS		3/14			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001511	OMIM:270100	IEA					P	HPO:iea[2009-02-17]
OMIM:270100	Heterotaxy, visceral, 5		HP:0001631	PMID:19064609	PCS		9/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0000006	PMID:19064609	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0002247	PMID:9354794	PCS		1/35			P	HPO:probinson[2021-09-18]
OMIM:270100	Heterotaxy, visceral, 5		HP:0002566	PMID:19064609	PCS		1/14			P	HPO:probinson[2021-09-18]
OMIM:614665	Meconium ileus		HP:0004401	PMID:22521417	PCS		11/15			P	HPO:skoehler[2013-05-29];HPO:probinson[2023-04-15]
OMIM:614665	Meconium ileus		HP:0003577	PMID:22521417	PCS		11/11			C	HPO:probinson[2023-04-15]
OMIM:614665	Meconium ileus		HP:0004388	OMIM:614665	TAS					P	HPO:skoehler[2013-06-11]
OMIM:614665	Meconium ileus		HP:0000007	PMID:22521417	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-15]
OMIM:614665	Meconium ileus		HP:0040128	PMID:22521417	PCS		0/15			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-15]
OMIM:614665	Meconium ileus		HP:0002028	PMID:22521417	PCS		2/15			P	HPO:probinson[2023-04-15]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0025484	PMID:7800007	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0000750	OMIM:609152	IEA					P	HPO:iea[2009-02-17]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0031506	PMID:7800007	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0025379	PMID:7800007	PCS		0/1			P	HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0200028	PMID:7800007	PCS		0/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0011788	PMID:7800007	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0032069	PMID:7800007	PCS		0/1			P	HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0001270	OMIM:609152	IEA					P	HPO:iea[2009-02-17]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0000836	PMID:7920658;PMID:7800007	PCS		11/11			P	HPO:probinson[2023-02-10];HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0001518	OMIM:609152	IEA					P	HPO:iea[2009-02-17]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0031098	PMID:7920658;PMID:7800007	PCS		11/11			P	HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0001649	PMID:7800007	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0005616	PMID:7800007	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0000752	PMID:7800007	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0003745	OMIM:609152	IEA					I	HPO:iea[2009-02-17]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0000520	PMID:7800007	PCS		0/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0008249	PMID:7800007	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0000006	PMID:7920658	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0000853	PMID:7920658;PMID:7800007	PCS		11/11			P	HPO:probinson[2023-02-10];HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0001249	PMID:7800007	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0003623	PMID:7800007	PCS		1/1			C	HPO:probinson[2023-02-10]
OMIM:609152	Hyperthyroidism, nonautoimmune		HP:0001622	PMID:7800007	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:151610	Levator-Medial rectus synkinesis		HP:0500043	OMIM:151610;PMID:3767680	IEA		20/20			P	HPO:lccarmody[2018-10-05];HPO:skoehler[2018-10-08]
OMIM:151610	Levator-Medial rectus synkinesis		HP:0000492	PMID:3767680	IEA					P	HPO:lccarmody[2018-10-05]
OMIM:151610	Levator-Medial rectus synkinesis		HP:0000508	PMID:3767680	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:151610	Levator-Medial rectus synkinesis		HP:0000006	OMIM:151610	IEA					I	HPO:iea[2009-02-17]
OMIM:151610	Levator-Medial rectus synkinesis		HP:0000478	OMIM:151610	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0001254	OMIM:274400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0000958	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0001537	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0000007	OMIM:274400	IEA					I	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0000821	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0000158	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0001510	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0002019	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0000853	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:274400	Thyroid hormonogenesis, genetic defect in, 1		HP:0001249	OMIM:274400	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003378	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0001265	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003477	PMID:30126838	PCS		2/2			P	HPO:probinson[2022-09-04]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0010628	PMID:30126838	PCS		1/2			P	HPO:probinson[2022-09-04]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003431	OMIM:118210	IEA				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003596	PMID:30126838	PCS		2/2			C	HPO:probinson[2022-09-04]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003376	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0001761	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003693	OMIM:118210	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003383	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0001284	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0002460	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003384	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003690	OMIM:118210	TAS					P	HPO:skoehler[2012-11-16]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003380	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0009027	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0009830	OMIM:118210	TAS					P	HPO:skoehler[2012-11-18]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0002936	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0000006	PMID:30126838	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0003677	OMIM:118210	IEA					C	HPO:iea[2009-02-17]
OMIM:118210	Charcot-Marie-Tooth disease, axonal, type 2A1		HP:0001765	OMIM:118210	IEA					P	HPO:iea[2009-02-17]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0002301	OMIM:609634	IEA					P	HPO:iea[2009-02-17]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0003621	PMID:16054936	PCS		16/17			C	HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0001250	OMIM:609634	IEA					P	HPO:iea[2009-02-17]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0002077	OMIM:609634	IEA		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0011462	PMID:16054936	PCS		1/17			C	HPO:probinson[2022-07-20]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0000618	OMIM:609634	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0000613	PMID:16054936	PCS		16/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0002183	PMID:16054936	PCS		16/17			P	HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0001269	OMIM:609634	IEA					P	HPO:iea[2009-02-17]
OMIM:609634	Migraine, familial hemiplegic, 3		HP:0000006	PMID:16054936	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0002069	OMIM:600176	IEA					P	HPO:iea[2009-02-17]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0007270	OMIM:600176	IEA					P	HPO:iea[2009-02-17]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0000924	OMIM:600176	IEA					P	HPO:iea[2009-02-17]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0001263	OMIM:600176	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0100702	OMIM:600176	TAS					P	HPO:skoehler[2013-05-31]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0000007	OMIM:600176	IEA					I	HPO:iea[2009-02-17]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0007069	OMIM:600176	IEA					P	HPO:iea[2009-02-17]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0001302	OMIM:600176	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600176	Pachygyria with impaired intellectual development, seizures, and arachnoid cysts		HP:0001249	OMIM:600176	IEA					P	HPO:skoehler[2010-06-18]
OMIM:614103	Lipedema		HP:0000969	OMIM:614103	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614103	Lipedema		HP:0100695	OMIM:614103	IEA					P	HPO:skoehler[2015-01-27]
OMIM:614103	Lipedema		HP:0000006	OMIM:614103	TAS					I	HPO:skoehler[2012-10-17]
OMIM:612572	Retinitis pigmentosa 46		HP:0001133	PMID:18806796	PCS		2/2			P	HPO:probinson[2013-04-06];HPO:probinson[2021-10-04]
OMIM:612572	Retinitis pigmentosa 46		HP:0000580	PMID:18806796	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:612572	Retinitis pigmentosa 46		HP:0000007	PMID:18806796	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612572	Retinitis pigmentosa 46		HP:0000505	PMID:18806796	PCS		2/2			P	HPO:probinson[2013-04-06];HPO:probinson[2021-10-04]
OMIM:612572	Retinitis pigmentosa 46		HP:0000510	PMID:18806796	PCS		2/2			P	HPO:probinson[2013-04-06];HPO:probinson[2021-10-04]
OMIM:612572	Retinitis pigmentosa 46		HP:0000543	PMID:18806796	PCS		2/2			P	HPO:probinson[2013-04-06];HPO:probinson[2021-10-04]
OMIM:612572	Retinitis pigmentosa 46		HP:0007787	PMID:18806796	PCS		1/2			P	HPO:probinson[2021-10-04]
OMIM:612572	Retinitis pigmentosa 46		HP:0007843	PMID:18806796	PCS		2/2			P	HPO:probinson[2013-04-06];HPO:probinson[2021-10-04]
OMIM:612572	Retinitis pigmentosa 46		HP:0000654	PMID:18806796	PCS		2/2			P	HPO:probinson[2013-04-06];HPO:probinson[2021-10-04]
OMIM:155310	Visceral myopathy 1		HP:0002014	OMIM:155310	TAS					P	HPO:skoehler[2014-06-24]
OMIM:155310	Visceral myopathy 1		HP:0002015	OMIM:155310	IEA					P	HPO:iea[2009-02-17]
OMIM:155310	Visceral myopathy 1		HP:0000021	OMIM:155310	TAS					P	HPO:skoehler[2014-01-28]
OMIM:155310	Visceral myopathy 1		HP:0001561	OMIM:155310	TAS					P	HPO:skoehler[2014-06-24]
OMIM:155310	Visceral myopathy 1		HP:0000076	OMIM:155310	IEA					P	HPO:iea[2009-02-17]
OMIM:155310	Visceral myopathy 1		HP:0030996	PMID:2806997	PCS		6/6			P	HPO:probinson[2021-06-27]
OMIM:155310	Visceral myopathy 1		HP:0004389	OMIM:155310	TAS					P	HPO:probinson[2017-05-29]
OMIM:155310	Visceral myopathy 1		HP:0004388	OMIM:155310	TAS					P	HPO:skoehler[2014-06-24]
OMIM:155310	Visceral myopathy 1		HP:0002013	OMIM:155310	TAS					P	HPO:skoehler[2014-06-24]
OMIM:155310	Visceral myopathy 1		HP:0002251	OMIM:155310	IEA					P	HPO:iea[2009-02-17]
OMIM:155310	Visceral myopathy 1		HP:0004395	OMIM:155310	TAS					P	HPO:skoehler[2014-06-24]
OMIM:155310	Visceral myopathy 1		HP:0003270	PMID:2806997	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:155310	Visceral myopathy 1		HP:6000072	OMIM:155310	TAS					P	HPO:probinson[2024-01-06]
OMIM:155310	Visceral myopathy 1		HP:0002019	PMID:2806997	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2021-06-27]
OMIM:155310	Visceral myopathy 1		HP:0002027	OMIM:155310	IEA					P	HPO:skoehler[2018-10-08]
OMIM:155310	Visceral myopathy 1		HP:0000006	OMIM:155310	TAS					I	HPO:iea[2009-02-17]
OMIM:155310	Visceral myopathy 1		HP:0001733	OMIM:155310	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:155310	Visceral myopathy 1		HP:0000126	OMIM:155310	TAS					P	HPO:skoehler[2014-06-24]
OMIM:155310	Visceral myopathy 1		HP:0000016	PMID:2806997	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:155310	Visceral myopathy 1		HP:0002578	PMID:2806997	PCS		1/6			P	HPO:probinson[2021-06-27]
OMIM:239500	Hyperprolinemia, type I		HP:0003137	PMID:11510941	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0002133	OMIM:239500	IEA					P	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0002353	OMIM:239500	IEA					P	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0000750	PMID:17412540	PCS		4/4			P	HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0001250	PMID:20524212	PCS		13/19			P	HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0001252	OMIM:239500	IEA					P	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0001263	PMID:17412540;PMID:20524212	PCS		14/23			P	HP:probinson[2019-03-02];HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0001251	PMID:17412540;PMID:20524212	PCS		7/23			P	HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0001290	OMIM:239500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:239500	Hyperprolinemia, type I		HP:0003080	OMIM:239500	IEA					P	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0100753	OMIM:239500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:239500	Hyperprolinemia, type I		HP:0000718	OMIM:239500	IEA					P	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0000729	PMID:20524212	PCS		3/19			P	HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0000007	OMIM:239500	IEA					I	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0000733	OMIM:239500	IEA					P	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0008358	PMID:17412540;PMID:20524212	PCS		14/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0000752	OMIM:239500	IEA					P	HPO:iea[2009-02-17]
OMIM:239500	Hyperprolinemia, type I		HP:0003108	PMID:23462603	PCS		2/3			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:239500	Hyperprolinemia, type I		HP:0001249	OMIM:239500	TAS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2013-03-24]
OMIM:614673	Microcephaly 8, primary, autosomal recessive		HP:0003577	PMID:22521416	PCS		2/2			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614673	Microcephaly 8, primary, autosomal recessive		HP:0000340	PMID:22521416	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614673	Microcephaly 8, primary, autosomal recessive		HP:0011451	PMID:22521416	PCS		2/2			P	HPO:probinson[2023-03-18]
OMIM:614673	Microcephaly 8, primary, autosomal recessive		HP:0000007	PMID:22521416	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614673	Microcephaly 8, primary, autosomal recessive		HP:0000278	OMIM:614673	TAS					P	HPO:skoehler[2012-10-17]
OMIM:226350	Eosinophilic fasciitis		HP:0045029	OMIM:226350	TAS					P	HPO:skoehler[2015-01-21]
OMIM:226350	Eosinophilic fasciitis		HP:0000007	OMIM:226350	IEA					I	HPO:iea[2009-02-17]
OMIM:601518	Prostate cancer, hereditary, 1		HP:0003581	PMID:11799394	PCS		11/11			C	HPO:probinson[2023-03-03]
OMIM:601518	Prostate cancer, hereditary, 1		HP:0012125	PMID:11799394	PCS		11/11			P	HPO:skoehler[2012-10-17]
OMIM:601518	Prostate cancer, hereditary, 1		HP:0000006	PMID:11799394	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-03-03]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0002421	PMID:23363473	PCS	HP:0003593	1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001332	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0002362	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:6000751	OMIM:618049	TAS					P	HPO:probinson[2024-08-03]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001252	PMID:23363473	PCS	HP:0003593	1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0003593	PMID:23363473	PCS		1/1			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001251	PMID:23363473	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:6000756	PMID:23363473	PCS		1/1			P	HPO:probinson[2024-06-29]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0011977	PMID:23363473	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0012332	PMID:23363473	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0000338	PMID:23363473	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0000975	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0025336	PMID:23363473	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0005968	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001347	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0002311	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0008936	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001300	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0031936	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001260	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001263	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0002075	PMID:23363473	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0010553	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0012378	PMID:23363473	PCS	HP:0003621	1/1			P	HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0000508	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0000007	PMID:23363473	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0025403	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001337	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-15]
OMIM:618049	Parkinsonism-dystonia, infantile, 2		HP:0001611	PMID:23363473	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-15]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0030667	OMIM:193235	IEA					P	HPO:skoehler[2015-12-30]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0007902	OMIM:193235	IEA					P	HPO:iea[2009-02-17]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0000541	OMIM:193235	IEA					P	HPO:iea[2009-02-17]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0000618	OMIM:193235	PCS		20/20			P	HPO:probinson[2012-04-07];HPO:iea[2009-02-17]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0007773	OMIM:193235	IEA					P	HPO:skoehler[2015-12-30]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0000554	OMIM:193235	PCS					P	HPO:probinson[2012-04-07]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0000006	OMIM:193235	PCS					I	HPO:probinson[2012-04-07]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0000512	OMIM:193235	PCS					P	HPO:probinson[2012-04-07]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0007778	OMIM:193235	IEA					P	HPO:skoehler[2015-12-30]
OMIM:193235	Vitreoretinopathy, neovascular inflammatory		HP:0007658	OMIM:193235	IEA					P	HPO:iea[2009-02-17]
OMIM:609622	Short QT syndrome 3		HP:0012232	PMID:22155372;PMID:15761194;PMID:23440193	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:609622	Short QT syndrome 3		HP:0003621	PMID:15761194	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:609622	Short QT syndrome 3		HP:0012663	PMID:22155372;PMID:15761194;PMID:23440193	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:609622	Short QT syndrome 3		HP:0031972	PMID:22155372;PMID:15761194;PMID:23440193	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:609622	Short QT syndrome 3		HP:0001962	PMID:22155372;PMID:15761194;PMID:23440193	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:609622	Short QT syndrome 3		HP:0004757	PMID:22155372;PMID:15761194;PMID:23440193	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:609622	Short QT syndrome 3		HP:0001645	PMID:22155372;PMID:15761194;PMID:23440193	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:609622	Short QT syndrome 3		HP:0000006	PMID:15761194	PCS					I	ORCID:0000-0002-0736-9199[2024-04-29]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0001562	PMID:24337657	PCS	HP:0011461	1/2			P	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0000021	PMID:24337657	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0003577	PMID:24337657	PCS		1/2			C	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0001399	PMID:24337657	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0004388	PMID:24337657	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0001409	PMID:24337657	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0000072	PMID:24337657	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0011461	PMID:24337657	PCS		1/2			C	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0000006	PMID:24337657	PCS					I	HPO:probinson[2021-08-22];HPO:probinson[2022-12-03]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0002566	PMID:24337657	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619431	Megacystis-microcolon-intestinal hypoperistalsis syndrome 5		HP:0000126	PMID:24337657	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:614115	Cortical malformations, occipital		HP:0000572	PMID:21572413	PCS		1/3		HP:0025303	P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0002069	PMID:21572413	PCS		3/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0003621	PMID:21572413	PCS		3/3			C	HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0002353	PMID:21572413	PCS					P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0001263	PMID:21572413	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0032909	PMID:21572413	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0000007	PMID:21572413	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0001302	PMID:21572413	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:614115	Cortical malformations, occipital		HP:0002126	PMID:21572413	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:614101	Plasma fibronectin deficiency		HP:0032463	PMID:2869211	PCS		8/8			P	HP:probinson[2019-04-19];HP:probinson[2019-04-19]
OMIM:614101	Plasma fibronectin deficiency		HP:0000006	PMID:2869211	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-04-19]
OMIM:617408	Diamond-Blackfan anemia 16		HP:0003577	PMID:25424902	PCS		1/1			C	HPO:probinson[2023-03-03]
OMIM:617408	Diamond-Blackfan anemia 16		HP:0001903	PMID:25424902	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:617408	Diamond-Blackfan anemia 16		HP:0001631	PMID:25424902	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:617408	Diamond-Blackfan anemia 16		HP:0001642	PMID:25424902	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:617408	Diamond-Blackfan anemia 16		HP:0000006	PMID:25424902	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:166900	Ovalocytosis, hereditary hemolytic		HP:0004445	PMID:5870194	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:166900	Ovalocytosis, hereditary hemolytic		HP:0001878	OMIM:166900	IEA					P	HPO:iea[2009-02-17]
OMIM:166900	Ovalocytosis, hereditary hemolytic		HP:0000006	OMIM:166900	IEA					I	HPO:iea[2009-02-17]
OMIM:609636	Alzheimer disease 10		HP:0002167	OMIM:609636	IEA					P	HPO:iea[2009-02-17]
OMIM:609636	Alzheimer disease 10		HP:0002354	OMIM:609636	IEA					P	HPO:iea[2009-02-17]
OMIM:609636	Alzheimer disease 10		HP:0002120	OMIM:609636	IEA					P	HPO:iea[2009-02-17]
OMIM:609636	Alzheimer disease 10		HP:0000726	OMIM:609636	IEA					P	HPO:iea[2009-02-17]
OMIM:609636	Alzheimer disease 10		HP:0000751	OMIM:609636	IEA					P	HPO:iea[2009-02-17]
OMIM:609636	Alzheimer disease 10		HP:0000006	OMIM:609636	IEA					I	HPO:iea[2009-02-17]
OMIM:609636	Alzheimer disease 10		HP:0002511	OMIM:609636	IEA					P	HPO:skoehler[2015-01-19]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0003577	PMID:26220973	PCS		4/4			C	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0004322	PMID:26220973	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0001250	PMID:26220973	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0005792	PMID:26220973	PCS		3/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0010544	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0100864	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0006150	PMID:26220973	PCS		1/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0032660	PMID:26220973	PCS		1/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0000519	PMID:26220973	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0002812	PMID:26220973	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0001324	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0001265	PMID:26220973	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0003202	PMID:26220973	PCS		3/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0000252	PMID:26220973	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0002136	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0001762	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0001761	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0003025	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0002099	PMID:26220973	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0001263	PMID:26220973	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0003021	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0005781	PMID:26220973	PCS		1/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0005041	PMID:26220973	PCS		1/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0011703	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0009830	PMID:26220973	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0000007	PMID:26220973	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0002868	PMID:26220973	PCS		1/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0002205	PMID:26220973	PCS		1/4			P	HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0002943	PMID:26220973	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0001510	PMID:26220973	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616716	Rhizomelic chondrodysplasia punctata, type 5		HP:0000666	PMID:26220973	PCS		1/4			P	HPO:probinson[2021-07-05]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0000572	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0003477	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0008209	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0001288	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0002120	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0001272	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0000141	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0001251	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0012108	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0000716	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0000739	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0000007	PMID:31778857	TAS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0000648	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619425	Mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)		HP:0002315	PMID:31778857	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000242	PMID:17850629	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000286	PMID:17850629	PCS		4/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001674	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000463	PMID:17850629	PCS		5/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001250	PMID:17850629	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001252	PMID:17850629	PCS		5/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0003593	PMID:17850629	PCS		1/5			C	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0410030	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001629	PMID:17850629	PCS		2/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001508	PMID:17850629	PCS		5/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0011461	PMID:17850629	PCS		2/5			C	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001647	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000218	PMID:17850629	PCS		1/4			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0030084	PMID:17850629	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001643	PMID:17850629	PCS		2/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001642	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001466	PMID:17850629	PCS					I	HPO:probinson[2022-09-04]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000358	PMID:17850629	PCS		5/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001007	PMID:17850629	PCS		4/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000456	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001644	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0003623	PMID:17850629	PCS		2/5			C	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000252	PMID:17850629	PCS		4/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000175	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000750	PMID:17850629	PCS		3/3			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0200128	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001263	PMID:17850629	PCS		5/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0011800	PMID:17850629	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0010773	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0011641	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0011229	PMID:17850629	PCS		4/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0012385	PMID:17850629	PCS		2/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001716	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000307	PMID:17850629	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0002007	PMID:17850629	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001631	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000369	PMID:17850629	PCS		5/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000347	PMID:17850629	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0000006	PMID:17850629	PCS					I	HPO:probinson[2022-09-04]
OMIM:619343	Chromosome 1p36 deletion syndrome, proximal		HP:0001655	PMID:17850629	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:606263	Paget disease of bone 4		HP:0002653	OMIM:606263	TAS					P	HPO:skoehler[2015-08-16]
OMIM:606263	Paget disease of bone 4		HP:0000365	OMIM:606263	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:606263	Paget disease of bone 4		HP:0003155	OMIM:606263	TAS					P	HPO:skoehler[2015-08-16]
OMIM:606263	Paget disease of bone 4		HP:0000006	OMIM:606263	TAS					I	HPO:skoehler[2015-12-30]
OMIM:606263	Paget disease of bone 4		HP:0002797	OMIM:606263	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613108	Candidiasis, familial, 4		HP:0000007	PMID:19864674	PCS					I	HPO:probinson[2013-01-09]
OMIM:613108	Candidiasis, familial, 4		HP:0012203	PMID:19864674	PCS					P	HPO:probinson[2013-03-12]
OMIM:613108	Candidiasis, familial, 4		HP:0012204	PMID:19864674	PCS					P	HPO:probinson[2013-03-12]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001177	OMIM:263630	IEA					P	HPO:iea[2009-02-17]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001561	OMIM:263630	IEA					P	HPO:iea[2009-02-17]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001792	OMIM:263630	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0000463	OMIM:263630	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001629	OMIM:263630	IEA					P	HPO:iea[2009-02-17]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0010066	OMIM:263630	TAS					P	HPO:skoehler[2013-03-15]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0000107	OMIM:263630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0000316	OMIM:263630	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001999	OMIM:263630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0003826	OMIM:263630	TAS		20/20			C	HPO:skoehler[2009-02-17];HPO:skoehler[2010-06-19]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0000007	OMIM:263630	IEA					I	HPO:iea[2009-02-17]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001407	OMIM:263630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001159	OMIM:263630	IEA					P	HPO:iea[2009-02-17]
OMIM:263630	Polysyndactyly with cardiac malformation		HP:0001631	OMIM:263630	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0008209	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000486	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000540	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000141	PMID:27081523	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000581	PMID:27081523;PMID:29339661	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000482	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000837	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000639	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000858	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000537	PMID:27081523;PMID:29339661	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000218	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000378	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0002553	OMIM:110100	TAS					P	HPO:probinson[2020-07-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000252	PMID:29339661	PCS		0/4			P	HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000013	OMIM:110100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000431	OMIM:110100	TAS					P	HPO:probinson[2012-05-01]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0045025	PMID:29339661	PCS		4/4			P	HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0005280	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000506	PMID:29339661	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0008222	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000508	PMID:27081523;PMID:29339661	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000568	OMIM:110100	IEA					P	HPO:iea[2009-02-17]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000769	PMID:27081523	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0000006	PMID:21325395	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-02-15]
OMIM:110100	Blepharophimosis, epicanthus inversus, and ptosis		HP:0002225	OMIM:110100	TAS					P	HPO:probinson[2020-07-17]
OMIM:608266	Parathyroid carcinoma		HP:0001442	PMID:14585940	PCS					I	HPO:probinson[2013-03-24]
OMIM:608266	Parathyroid carcinoma		HP:0006780	OMIM:608266	TAS					P	HPO:probinson[2013-01-09]
OMIM:608266	Parathyroid carcinoma		HP:0000843	OMIM:608266	TAS					P	HPO:probinson[2013-03-24]
OMIM:608266	Parathyroid carcinoma		HP:0003072	OMIM:608266	TAS					P	HPO:probinson[2013-03-24]
OMIM:608266	Parathyroid carcinoma		HP:0000006	PMID:14585940	PCS					I	HPO:probinson[2013-03-24]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0001771	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003236	OMIM:607155	TAS					P	HPO:probinson[2012-04-08]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003551	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003394	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003828	OMIM:607155	TAS					M	HPO:skoehler[2012-10-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0032341	OMIM:607155	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003749	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0002515	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003307	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0000158	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0002359	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003547	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003701	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0002877	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0001644	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003326	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0002650	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0001288	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003560	OMIM:607155	TAS					P	HPO:probinson[2012-04-08]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0005162	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0002091	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0002808	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0002948	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0008981	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0000007	OMIM:607155	IEA					I	HPO:probinson[2009-02-17]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0030051	OMIM:607155	TAS					P	HPO:skoehler[2014-11-27]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0008305	OMIM:607155	TAS		25%			P	HPO:probinson[2012-04-08]
OMIM:607155	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5		HP:0003733	OMIM:607155	IEA					P	HPO:probinson[2009-02-17]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0003621	PMID:11407343	PCS					C	HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0005165	PMID:11407343	PCS					P	HPO:probinson[2012-06-10];HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0001716	PMID:11748095;PMID:11407343	PCS		35/35			P	HPO:probinson[2021-09-23];HPO:skoehler[2015-01-21];HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0011463	PMID:11748095	PCS		3/3			C	HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0011462	PMID:11407343	PCS					C	HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0006684	PMID:11407343	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0004309	PMID:11748095;PMID:11407343	PCS		27/27			P	HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0004749	PMID:11748095	PCS		2/3			P	HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0001962	PMID:11407343	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0004757	PMID:11748095;PMID:11407343	PCS		15/34			P	HPO:probinson[2021-09-23];HPO:iea[2009-02-17];HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0006677	PMID:11407343	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0001279	PMID:11748095;PMID:11407343	PCS		14/26		HP:0031796;HP:0031796	P	HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0000006	PMID:11407343	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2021-09-23]
OMIM:194200	Wolff-Parkinson-White syndrome		HP:0001645	PMID:11407343	PCS		6/31			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-09-23]
OMIM:618075	Epilepsy, familial adult myoclonic, 7		HP:0001250	PMID:29507423	PCS		HP:0040283			P	HPO:probinson[2020-05-15]
OMIM:618075	Epilepsy, familial adult myoclonic, 7		HP:0033054	PMID:29507423	PCS					P	HPO:probinson[2020-08-13]
OMIM:618075	Epilepsy, familial adult myoclonic, 7		HP:0003581	PMID:29507423	PCS					C	HPO:probinson[2020-05-15]
OMIM:618075	Epilepsy, familial adult myoclonic, 7		HP:0000006	PMID:29507423	PCS					I	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:613120	Brugada syndrome 7		HP:0004754	PMID:21051419	PCS		2/3			P	HPO:probinson[2022-07-10]
OMIM:613120	Brugada syndrome 7		HP:0003596	PMID:21051419	PCS		1/3			C	HPO:probinson[2022-07-10]
OMIM:613120	Brugada syndrome 7		HP:0012251	OMIM:613120	TAS					P	HPO:probinson[2013-06-02]
OMIM:613120	Brugada syndrome 7		HP:0004749	OMIM:613120	TAS					P	HPO:probinson[2013-06-02]
OMIM:613120	Brugada syndrome 7		HP:0025710	PMID:21051419	PCS		2/3			C	HPO:probinson[2022-07-10]
OMIM:613120	Brugada syndrome 7		HP:0004757	PMID:21051419	PCS		1/3			P	HPO:probinson[2022-07-10]
OMIM:613120	Brugada syndrome 7		HP:0000006	PMID:21051419	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-10]
OMIM:613120	Brugada syndrome 7		HP:0034308	PMID:21051419	PCS		1/3			P	HPO:probinson[2022-09-05]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0000054	OMIM:614897	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0030344	PMID:22416012	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0030341	PMID:22416012	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0040171	PMID:22416012	PCS		2/2	MALE		P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0032466	PMID:22416012	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0025708	PMID:22416012	PCS		3/3			C	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0000458	PMID:22416012	PCS		1/3			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0004409	PMID:22416012	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0008214	PMID:22416012	PCS		1/1			P	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0008734	OMIM:614897	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0001335	PMID:22416012	PCS		0/3			P	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0000135	PMID:22416012	PCS		2/3			P	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0040326	PMID:22416012	PCS		2/3			P	HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0000028	PMID:22416012	PCS		1/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0000006	PMID:22416012	PCS					I	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0000027	OMIM:614897	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614897	Hypogonadotropic hypogonadism 16 with or without anosmia		HP:0000786	PMID:22416012	PCS		1/1			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-10-02]
OMIM:615551	Episodic pain syndrome, familial, 2		HP:0003581	PMID:23115331	PCS					C	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-02]
OMIM:615551	Episodic pain syndrome, familial, 2		HP:0000006	PMID:23115331	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-02]
OMIM:615551	Episodic pain syndrome, familial, 2		HP:0012534	PMID:23115331	PCS		3/3			P	HPO:probinson[2021-05-02]
OMIM:615237	Congenital short bowel syndrome		HP:0030897	OMIM:615237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615237	Congenital short bowel syndrome		HP:0003577	PMID:33384711	PCS		1/2			C	HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0002587	PMID:33384711	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0002013	PMID:31061750	PCS		1/1			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0002570	OMIM:615237	TAS					P	HPO:skoehler[2015-08-16]
OMIM:615237	Congenital short bowel syndrome		HP:0003593	PMID:33384711	PCS		1/2			C	HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0003270	PMID:31061750	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0030914	OMIM:615237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615237	Congenital short bowel syndrome		HP:0030889	PMID:33384711;PMID:35111702;PMID:31061750	PCS		5/5			P	HPO:probinson[2017-05-28];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0001508	PMID:33384711;PMID:31061750	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0011100	PMID:31061750	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0001944	PMID:31061750	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0000007	PMID:22155368	PCS					I	HPO:skoehler[2016-02-01];HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0001984	PMID:31061750	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0002566	PMID:33384711;PMID:35111702;PMID:31061750	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0001942	PMID:33384711;PMID:31061750	PCS		3/3			P	HPO:probinson[2022-02-27]
OMIM:615237	Congenital short bowel syndrome		HP:0002028	PMID:35111702;PMID:31061750	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:163850	Noduli cutanei, multiple, with urinary tract abnormalities		HP:0000081	OMIM:163850	IEA					P	HPO:iea[2009-02-17]
OMIM:163850	Noduli cutanei, multiple, with urinary tract abnormalities		HP:0000006	OMIM:163850	IEA					I	HPO:iea[2009-02-17]
OMIM:163850	Noduli cutanei, multiple, with urinary tract abnormalities		HP:0000126	OMIM:163850	IEA					P	HPO:iea[2009-02-17]
OMIM:163850	Noduli cutanei, multiple, with urinary tract abnormalities		HP:0000951	OMIM:163850	IEA					P	HPO:iea[2009-02-17]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0003577	PMID:20524213	PCS		1/1			C	HPO:probinson[2023-07-18]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0012120	PMID:20524213	TAS	HP:0003623	1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-07-24];HPO:probinson[2022-06-14]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0012120	PMID:22819238	PCS		1/1			P	HPO:probinson[2022-06-14]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0012120	PMID:20524213	PCS		1/1			P	HPO:probinson[2023-07-18]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0003593	PMID:22819238	PCS		1/1			C	HPO:probinson[2022-06-14]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0002160	PMID:22819238;PMID:20524213	PCS		1/2			P	HPO:probinson[2022-06-14]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0000007	PMID:20524213	TAS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-07-24]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0002912	PMID:22819238	PCS		1/1			P	HPO:probinson[2022-06-14]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0034985	PMID:20524213	PCS		4/4			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:613646	Methylmalonic aciduria, transient, due to transcobalamin receptor defect		HP:0003623	PMID:20524213	PCS		1/1			C	HPO:probinson[2022-06-14]
OMIM:614129	Perrault syndrome 3		HP:0000252	PMID:23541340	PCS		3/10			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0000013	PMID:23541340	PCS		3/9			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0004322	PMID:23541340	PCS		3/10			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0000815	PMID:23541340	PCS					P	HPO:probinson[2013-09-14];HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0001250	PMID:23541340	PCS		3/10			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0000407	PMID:23541340	PCS	HP:0003577	10/10			P	HPO:probinson[2013-09-14];HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0011969	PMID:23541340	PCS		7/8			P	HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0008232	PMID:23541340	PCS		8/8			P	HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0000007	PMID:23541340	PCS					I	HPO:probinson[2013-09-14];HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0010464	PMID:23541340	PCS		1/9			P	HPO:probinson[2023-02-11]
OMIM:614129	Perrault syndrome 3		HP:0000786	PMID:23541340	PCS		3/9			P	HPO:probinson[2013-09-14];HPO:probinson[2023-02-11]
OMIM:159500	Myelinated optic nerve fibers		HP:0000006	OMIM:159500	IEA					I	HPO:iea[2009-02-17]
OMIM:159500	Myelinated optic nerve fibers		HP:0000478	OMIM:159500	IEA					P	HPO:iea[2009-02-17]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000582	PMID:29961568	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000486	PMID:29961568	PCS		4/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0001250	PMID:29961568	PCS	HP:0011463	4/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0001290	PMID:29961568	PCS		4/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0008093	PMID:29961568	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000957	PMID:29961568	PCS		2/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0002816	PMID:29961568	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0012450	PMID:29961568	PCS		4/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0007663	PMID:29961568	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0002119	PMID:29961568	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0025336	PMID:29961568	PCS		2/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0006610	PMID:29961568	PCS		2/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0001763	PMID:29961568	PCS		3/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0002136	PMID:29961568	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000010	PMID:29961568	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000750	PMID:29961568	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0005643	PMID:29961568	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0002376	PMID:29961568	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0031936	PMID:29961568	PCS		5/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0001382	PMID:29961568	PCS		3/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0011968	PMID:29961568	PCS		3/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000490	PMID:29961568	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000592	PMID:29961568	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0003186	PMID:29961568	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0011800	PMID:29961568	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0001182	PMID:29961568	PCS		2/4			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0100716	PMID:29961568	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000520	PMID:29961568	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618707	Neurodevelopmental disorder with absent language and variable seizures		HP:0000006	PMID:29961568	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:613652	C1q deficiency		HP:0002960	OMIM:613652	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613652	C1q deficiency		HP:0005356	OMIM:613652	TAS					P	HPO:probinson[2013-12-15]
OMIM:613652	C1q deficiency		HP:0000793	OMIM:613652	TAS		HP:0040283			P	HPO:probinson[2013-12-15]
OMIM:613652	C1q deficiency		HP:0002719	OMIM:613652	TAS					P	HPO:probinson[2013-12-15]
OMIM:613652	C1q deficiency		HP:0000007	OMIM:613652	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613652	C1q deficiency		HP:0002725	OMIM:613652	TAS		HP:0040283			P	HPO:probinson[2013-12-15]
OMIM:228355	Fetal iodine deficiency disorder		HP:0001264	OMIM:228355	IEA					P	HPO:iea[2009-02-17]
OMIM:228355	Fetal iodine deficiency disorder		HP:0000365	OMIM:228355	IEA					P	HPO:iea[2009-02-17]
OMIM:228355	Fetal iodine deficiency disorder		HP:0008251	OMIM:228355	TAS					P	HPO:probinson[2009-02-17]
OMIM:228355	Fetal iodine deficiency disorder		HP:0001939	OMIM:228355	IEA					P	HPO:iea[2009-02-17]
OMIM:228355	Fetal iodine deficiency disorder		HP:0000007	OMIM:228355	IEA					I	HPO:iea[2009-02-17]
OMIM:228355	Fetal iodine deficiency disorder		HP:0000851	OMIM:228355	TAS					P	HPO:probinson[2009-02-17]
OMIM:228355	Fetal iodine deficiency disorder		HP:0001249	OMIM:228355	IEA					P	HPO:iea[2009-02-17]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0002652	OMIM:102510	IEA					P	HPO:iea[2009-02-17]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0001770	OMIM:102510	IEA					P	HPO:iea[2009-02-17]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0005048	OMIM:102510	IEA					P	HPO:iea[2009-02-17]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0001241	OMIM:102510	IEA					P	HPO:skoehler[2012-10-09]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0011304	OMIM:102510	TAS					P	HPO:probinson[2012-06-08]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0009467	OMIM:102510	TAS					P	HPO:probinson[2012-06-08]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0006101	OMIM:102510	IEA					P	HPO:skoehler[2010-06-20]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0009611	OMIM:102510	IEA					P	HPO:iea[2009-02-17]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0009778	OMIM:102510	TAS					P	HPO:probinson[2012-06-08]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0004614	OMIM:102510	TAS					P	HPO:probinson[2012-06-10]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0000006	OMIM:102510	IEA					I	HPO:iea[2009-02-17]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0000765	OMIM:102510	IEA					P	HPO:iea[2009-02-17]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0003468	OMIM:102510	IEA					P	HPO:skoehler[2012-10-09]
OMIM:102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0004601	OMIM:102510	TAS					P	HPO:probinson[2009-02-17]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001892	PMID:16896922	PCS		11/62			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000121	PMID:16896922	PCS		6/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000340	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0003577	PMID:16896922	PCS					C	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000365	PMID:16896922	PCS		4/62			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0003355	PMID:16896922	PCS		62/62			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001252	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001290	OMIM:208085	TAS					P	HPO:skoehler[2017-07-13]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0034714	OMIM:208085	TAS					P	HPO:probinson[2023-06-05]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0200084	PMID:16896922	PCS		12/16			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001508	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001629	PMID:16896922	PCS		2/62			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001947	PMID:16896922	PCS		62/62			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001944	OMIM:208085	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001522	PMID:16896922	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0002910	PMID:16896922	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001884	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000952	PMID:16896922	PCS		62/62			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001942	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001667	OMIM:208085	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0002611	PMID:16896922	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001562	PMID:16896922	PCS		10/62			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001385	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000252	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0005248	PMID:16896922	PCS		7/16			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000112	OMIM:208085	IEA					P	HPO:iea[2009-02-17]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0009806	OMIM:208085	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0005565	PMID:16896922	PCS		6/14			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001263	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0030948	PMID:16896922	PCS		0/62			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000092	PMID:16896922	PCS		2/16			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0002908	PMID:16896922	PCS		62/62			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0008064	PMID:16896922	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001518	PMID:16896922	PCS	HP:0003577	30/62			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001339	OMIM:208085	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0002804	PMID:16896922	PCS		60/62			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000007	PMID:15052268	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001631	OMIM:208085;PMID:16896922	PCS		12/72			P	HPO:probinson[2022-08-28];HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001873	PMID:16896922	PCS		7/62			P	HPO:probinson[2022-08-28]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000369	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0000347	OMIM:208085	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208085	Arthrogryposis, renal dysfunction, and cholestasis 1		HP:0001655	PMID:16896922	PCS		2/62			P	HPO:probinson[2022-08-28]
OMIM:271220	Spinal muscular atrophy, scapuloperoneal		HP:0009049	OMIM:271220	IEA					P	HPO:iea[2009-02-17]
OMIM:271220	Spinal muscular atrophy, scapuloperoneal		HP:0000007	OMIM:271220	IEA					I	HPO:iea[2009-02-17]
OMIM:271220	Spinal muscular atrophy, scapuloperoneal		HP:0007269	OMIM:271220	IEA					P	HPO:iea[2009-02-17]
OMIM:271220	Spinal muscular atrophy, scapuloperoneal		HP:0009060	OMIM:271220	IEA					P	HPO:iea[2009-02-17]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0008947	OMIM:614883	IEA					P	HPO:skoehler[2013-01-09]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0001410	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0000463	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0001250	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0000260	OMIM:614883	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0001263	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0005562	OMIM:614883	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0006829	OMIM:614883	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0005280	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0001508	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0000239	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0001339	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0100729	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0000107	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0000348	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0000007	OMIM:614883	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0003429	PMID:9194444	PCS					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0002910	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0002126	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0000325	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614883	Peroxisome biogenesis disorder 11A (Zellweger)		HP:0002104	OMIM:614883	IEA					P	HPO:skoehler[2013-01-11]
OMIM:223200	Disorganization, mouse, homolog of		HP:0001012	OMIM:223200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:223200	Disorganization, mouse, homolog of		HP:0012033	OMIM:223200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0000175	OMIM:223200	TAS					P	HPO:skoehler[2010-06-18]
OMIM:223200	Disorganization, mouse, homolog of		HP:0005765	OMIM:223200	IEA					P	HPO:iea[2009-02-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0100524	OMIM:223200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0000407	OMIM:223200	IEA					P	HPO:iea[2009-02-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0001161	OMIM:223200	IEA					P	HPO:iea[2009-02-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0002827	OMIM:223200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0000007	OMIM:223200	IEA					I	HPO:iea[2009-02-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0000204	OMIM:223200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:223200	Disorganization, mouse, homolog of		HP:0005217	OMIM:223200	IEA					P	HPO:iea[2009-02-17]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0003774	PMID:29706351	PCS		7/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0003676	PMID:29706351	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0000083	PMID:29706351	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0003581	PMID:29706351	PCS		22/22			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0000822	PMID:29706351	PCS		11/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0001407	PMID:29706351	PCS		9/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0012213	PMID:29706351	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0000113	PMID:29706351	PCS		20/21			P	HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0001997	PMID:29706351	PCS		2/23			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618061	Polycystic kidney disease 6 with or without polycystic liver disease		HP:0000006	PMID:29706351	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-02-18]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000286	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001034	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0003510	PMID:26248010	PCS		8/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0002650	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0011968	PMID:26248010	PCS					P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000085	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0004691	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001290	PMID:26248010	PCS		4/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001270	PMID:26248010	PCS		2/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001508	PMID:26248010	PCS	HP:0003593	8/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000957	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0003307	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0030084	PMID:26248010	PCS		2/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000268	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001511	PMID:26248010	PCS	HP:0030674				P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000278	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000358	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000325	PMID:26248010	PCS		1/8			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0000252	PMID:36965478	PCS		8/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0002059	PMID:36965478	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0004322	PMID:36965478	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0001288	PMID:36965478	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0001332	PMID:36965478	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0001272	PMID:36965478	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0001260	PMID:36965478	PCS		8/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0001285	PMID:36965478	PCS		6/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0003593	PMID:36965478	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0033044	PMID:36965478	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0011463	PMID:36965478	PCS		7/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0034332	PMID:36965478	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0000007	PMID:36965478	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0002307	PMID:36965478	PCS		7/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0001257	PMID:36965478	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620515	Neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction		HP:0001347	PMID:36965478	PCS		9/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0020072	PMID:22174160	PCS		3/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0002783	PMID:22294732;PMID:22174160	PCS		2/7			P	HPO:probinson[2023-06-18];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0001890	PMID:22174160	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0003593	PMID:22174160	PCS		1/4			C	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0032185	PMID:22174160	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0032163	PMID:22174160	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0011463	PMID:22294732;PMID:22174160	PCS		5/7			C	HPO:probinson[2023-06-17];HPO:probinson[2023-06-18];HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0002718	PMID:22294732	PCS		3/3			P	HPO:skoehler[2013-02-24];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0100806	PMID:22294732	PCS		2/3			P	HPO:probinson[2023-06-17];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0001888	PMID:22174160;OMIM:614868	PCS		11/14			P	HPO:probinson[2023-06-18];HPO:skoehler[2013-02-24]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0006532	PMID:22294732;PMID:22174160	PCS		3/7			P	HPO:probinson[2023-06-18];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0200043	PMID:22294732	PCS		3/3			P	HPO:skoehler[2013-02-24];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0005523	PMID:22174160	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0003621	PMID:22294732	PCS		1/3			C	HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0001684	PMID:22294732	PCS		2/3			P	HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0002110	PMID:22174160	PCS		3/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0001581	PMID:22294732;PMID:22174160	PCS		3/7			P	HPO:probinson[2023-06-18];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0011108	PMID:22294732;PMID:22174160	PCS		3/7			P	HPO:probinson[2023-06-18];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0011107	PMID:22174160	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0012189	PMID:22174160	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0002728	PMID:22294732	PCS		3/3			P	HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0000007	PMID:22294732	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0001954	PMID:22294732	PCS		1/3			P	HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0004429	PMID:22294732	PCS		3/3			P	HPO:skoehler[2013-02-24];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0002788	PMID:22294732	PCS		2/3			P	HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0002841	OMIM:614868	TAS					P	HPO:skoehler[2013-02-24]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0001875	PMID:22294732;PMID:22174160	PCS		5/7			P	HPO:probinson[2023-06-18];HPO:skoehler[2013-02-24]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0002721	PMID:22294732	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-06-17]
OMIM:614868	Immunodeficiency-110 with lymphoproliferation		HP:0001655	PMID:22294732	PCS		3/3			P	HPO:probinson[2023-06-17]
OMIM:613861	Retinitis pigmentosa 59		HP:0008936	OMIM:613861	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613861	Retinitis pigmentosa 59		HP:0001133	PMID:21295283	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:613861	Retinitis pigmentosa 59		HP:0003621	PMID:21295283	PCS		3/3			C	HPO:probinson[2022-12-14]
OMIM:613861	Retinitis pigmentosa 59		HP:0000054	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613861	Retinitis pigmentosa 59		HP:0000662	PMID:21295283	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:613861	Retinitis pigmentosa 59		HP:0011968	OMIM:613861	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613861	Retinitis pigmentosa 59		HP:0001250	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613861	Retinitis pigmentosa 59		HP:0000083	OMIM:613861	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613861	Retinitis pigmentosa 59		HP:0002240	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613861	Retinitis pigmentosa 59		HP:0011505	OMIM:613861	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613861	Retinitis pigmentosa 59		HP:0001508	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613861	Retinitis pigmentosa 59		HP:0000407	OMIM:613861	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613861	Retinitis pigmentosa 59		HP:0000007	PMID:21295283	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:613861	Retinitis pigmentosa 59		HP:0007663	PMID:21295283	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:613861	Retinitis pigmentosa 59		HP:0001511	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613861	Retinitis pigmentosa 59		HP:0000510	OMIM:613861	IEA		3/3			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-12-14]
OMIM:613861	Retinitis pigmentosa 59		HP:0002910	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613861	Retinitis pigmentosa 59		HP:0001257	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613861	Retinitis pigmentosa 59		HP:0000028	OMIM:613861	IEA					P	HPO:skoehler[2018-10-08]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001891	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001894	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001596	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0003256	OMIM:212750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0004322	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001250	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001271	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001251	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0003270	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0100651	OMIM:212750	TAS					P	HPO:skoehler[2013-03-14]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0000939	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0100502	OMIM:212750	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0008151	OMIM:212750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0000716	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001508	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0100646	OMIM:212750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0000739	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0006297	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001426	OMIM:212750	IEA					I	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0008897	OMIM:212750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0100507	OMIM:212750	TAS					P	HPO:skoehler[2013-09-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001824	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002514	OMIM:212750	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:skoehler[2010-06-18]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002910	OMIM:212750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0003645	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002014	OMIM:212750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002013	OMIM:212750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0004298	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002570	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0011107	OMIM:212750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0100512	OMIM:212750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0011892	OMIM:212750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0010280	OMIM:212750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002829	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002608	OMIM:212750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0000789	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002748	OMIM:212750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0000007	OMIM:212750	IEA					I	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0000964	OMIM:212750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0000823	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002901	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0001972	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002027	OMIM:212750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002665	OMIM:212750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212750	Celiac disease, susceptibility to, 1		HP:0002720	OMIM:212750	IEA					P	HPO:iea[2009-02-17]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0003621	PMID:28280076	PCS		3/7			C	HPO:probinson[2022-07-10]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0003596	PMID:28280076	PCS		2/7			C	HPO:probinson[2022-07-10]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0005133	PMID:28280076	PCS					P	HPO:probinson[2020-08-11]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0011462	PMID:28280076	PCS		2/7			C	HPO:probinson[2022-07-10]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0006682	PMID:28280076	PCS		2/7			P	HPO:probinson[2020-08-11]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0100749	PMID:28280076	PCS		4/7			P	HPO:probinson[2020-08-11]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0011713	PMID:28280076	PCS		4/7			P	HPO:probinson[2020-08-11]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0031972	PMID:28280076	PCS		2/7			P	HPO:probinson[2020-08-11]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0001962	PMID:28280076	PCS		7/7			P	HPO:probinson[2020-08-11]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0000006	PMID:28280076	PCS					I	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618920	Arrhythmogenic right ventricular dysplasia, familial, 14		HP:0004756	PMID:28280076	PCS		2/7			P	HPO:probinson[2020-08-11]
OMIM:185480	Suprabulbar paresis, congenital		HP:0000252	OMIM:185480	IEA					P	HPO:iea[2009-02-17]
OMIM:185480	Suprabulbar paresis, congenital		HP:0002353	OMIM:185480	IEA					P	HPO:iea[2009-02-17]
OMIM:185480	Suprabulbar paresis, congenital		HP:0001250	OMIM:185480	IEA					P	HPO:iea[2009-02-17]
OMIM:185480	Suprabulbar paresis, congenital		HP:0001260	OMIM:185480	IEA					P	HPO:iea[2009-02-17]
OMIM:185480	Suprabulbar paresis, congenital		HP:0002307	OMIM:185480	IEA					P	HPO:iea[2009-02-17]
OMIM:185480	Suprabulbar paresis, congenital		HP:0001324	OMIM:185480	IEA					P	HPO:skoehler[2010-06-20]
OMIM:185480	Suprabulbar paresis, congenital		HP:0000006	OMIM:185480	IEA					I	HPO:iea[2009-02-17]
OMIM:185480	Suprabulbar paresis, congenital		HP:0001249	OMIM:185480	IEA					P	HPO:iea[2009-02-17]
OMIM:621179	Diarrhea 15, congenital 		HP:0002014	PMID:40174224	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621179	Diarrhea 15, congenital 		HP:0003593	PMID:40174224	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621179	Diarrhea 15, congenital 		HP:0033994	PMID:40174224	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621179	Diarrhea 15, congenital 		HP:0000007	PMID:40174224	PCS					I	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:181180	Say syndrome		HP:0000175	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0000252	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0004322	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0009463	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0009882	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0000800	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0001182	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0000400	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0000006	OMIM:181180	IEA					I	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0000347	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0002049	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:181180	Say syndrome		HP:0000951	OMIM:181180	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0000164	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0001773	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0004322	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0001332	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0001250	PMID:34778139	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:312750	Rett syndrome		HP:0002120	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0005135	OMIM:312750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002066	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002020	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0010521	OMIM:312750	IEA					P	HPO:skoehler[2010-06-18]
OMIM:312750	Rett syndrome		HP:0011463	PMID:34778139	PCS		1/1			C	HPO:probinson[2022-09-26]
OMIM:312750	Rett syndrome		HP:0012171	PMID:9792883;PMID:34778139	PCS		3/3			P	HPO:probinson[2022-09-26]
OMIM:312750	Rett syndrome		HP:0001423	PMID:9792883	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:312750	Rett syndrome		HP:0004879	PMID:9792883	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:312750	Rett syndrome		HP:0002019	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0003202	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002333	PMID:9792883	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-26]
OMIM:312750	Rett syndrome		HP:0003763	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002078	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002650	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002353	OMIM:312750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002376	PMID:9792883;PMID:34778139	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:312750	Rett syndrome		HP:0005484	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0005184	OMIM:312750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002808	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0000729	OMIM:312750	TAS					P	HPO:skoehler[2014-04-04]
OMIM:312750	Rett syndrome		HP:0001257	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:312750	Rett syndrome		HP:0002104	OMIM:312750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:312750	Rett syndrome		HP:0004326	OMIM:312750	IEA					P	HPO:iea[2009-02-17]
OMIM:177170	Pseudoachondroplasia		HP:0002663	PMID:20301660	PCS					P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0003016	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0001377	PMID:27432013	PCS		3/6			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0001498	PMID:20301660	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0001156	PMID:27432013	PCS		6/6			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0003311	OMIM:177170	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0002341	OMIM:177170	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0004042	PMID:21599986	PCS					P	HPO:probinson[2015-03-21]
OMIM:177170	Pseudoachondroplasia		HP:0010049	PMID:20301660	PCS					P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0003093	PMID:20301660	PCS					P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0012307	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0010585	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0009487	OMIM:177170	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0002816	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0002938	PMID:20301660	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0009882	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0008873	PMID:20301660	PCS	HP:0011463				P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0002834	PMID:21599986	PCS					P	HPO:probinson[2015-03-21]
OMIM:177170	Pseudoachondroplasia		HP:0002515	PMID:20301660	PCS	HP:0011463				P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0002758	PMID:27432013;PMID:20301660	PCS		11/16			P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0002857	OMIM:177170	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0001249	PMID:27432013	PCS		0/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0004019	PMID:21599986	PCS					P	HPO:probinson[2015-03-21]
OMIM:177170	Pseudoachondroplasia		HP:0009803	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0003026	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0004236	PMID:20301660	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0003049	OMIM:177170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:177170	Pseudoachondroplasia		HP:0002650	PMID:27432013	PCS		6/6			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0002970	PMID:27432013	PCS		5/6			P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0003025	PMID:27432013	PCS		5/6			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0001382	PMID:20301660	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0010236	OMIM:177170	TAS					P	HPO:probinson[2015-03-08];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0005063	OMIM:177170	TAS					P	HPO:skoehler[2015-04-05]
OMIM:177170	Pseudoachondroplasia		HP:0011405	OMIM:177170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:177170	Pseudoachondroplasia		HP:0100168	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0002829	PMID:20301660	PCS	HP:0011463				P	HPO:probinson[2010-07-12];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0002808	OMIM:177170	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0010582	PMID:27432013	PCS		5/6			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0000926	PMID:27432013	PCS	HP:0011463	5/6			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0006467	PMID:27432013	PCS		2/6			P	HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0000763	OMIM:177170	TAS					P	HPO:probinson[2010-07-12];HPO:probinson[2024-03-08]
OMIM:177170	Pseudoachondroplasia		HP:0000006	OMIM:177170	TAS					I	HPO:probinson[2009-02-17]
OMIM:177170	Pseudoachondroplasia		HP:0004568	PMID:27432013	PCS		5/6			P	HPO:probinson[2012-07-28];HP:probinson[2019-03-01]
OMIM:177170	Pseudoachondroplasia		HP:0003414	OMIM:177170	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:620501	Ziegler-Huang syndrome		HP:0000054	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0010627	PMID:36821639	PCS		1/2			P	HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0002750	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0030674	PMID:36821639	PCS		2/2			C	HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0011904	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0031688	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0007099	PMID:36821639	PCS		1/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0008232	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0000007	PMID:36821639	PCS					I	HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0005528	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0001511	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0001510	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0000135	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0001972	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0000028	PMID:36821639	PCS		1/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0005548	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11];HPO:probinson[2024-03-11]
OMIM:620501	Ziegler-Huang syndrome		HP:0001875	PMID:36821639	PCS		2/2			P	HPO:probinson[2024-03-11]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001773	PMID:17236139	PCS		7/14			P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0004322	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001250	PMID:17236139	PCS	HP:0003593	8/11			P	HPO:probinson[2017-05-29]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0002066	PMID:17236139	PCS		6/12			P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001252	OMIM:300354	TAS					P	HPO:skoehler[2015-04-05]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0004482	OMIM:300354	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001290	OMIM:300354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000280	OMIM:300354	TAS					P	HPO:skoehler[2015-04-05]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0012743	PMID:26522830	PCS		15/19			P	HPO:skoehler[2015-01-20]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000718	PMID:17236139	PCS		12/15			P	HPO:probinson[2017-05-29]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000712	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0002539	OMIM:300354	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000158	OMIM:300354	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000752	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0008734	PMID:17236139	PCS		10/15			P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001763	PMID:17236139	PCS		1/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001249	PMID:17236139	PCS		18/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000054	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001344	OMIM:300354	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0002079	OMIM:300354	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000771	PMID:17236139	PCS		7/10			P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001382	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001065	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001419	PMID:17236139	PCS					I	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001852	OMIM:300354	IEA		11/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-20]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000047	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001337	OMIM:300354	PCS		11/13			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0002500	OMIM:300354	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001156	PMID:17273978	PCS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001270	PMID:17236139	PCS		5/5			P	HPO:probinson[2017-05-29]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000414	OMIM:300354	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0002119	OMIM:300354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000179	PMID:17236139	PCS		6/17			P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000135	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000377	OMIM:300354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0006855	OMIM:300354	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000154	OMIM:300354	TAS					P	HPO:skoehler[2015-04-05]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000750	PMID:17236139	PCS		18/18			P	HPO:probinson[2017-05-29]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0001761	OMIM:300354	IEA		7/8			P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0005280	OMIM:300354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0002808	PMID:17236139	PCS		3/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000348	OMIM:300354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000823	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0200055	OMIM:300354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0002126	OMIM:300354	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000303	OMIM:300354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0000028	OMIM:300354	IEA					P	HPO:iea[2009-02-17]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0009879	OMIM:300354	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300354	Intellectual developmental disorder, X-linked syndromic, Cabezas type		HP:0008944	PMID:17236139	PCS		7/12			P	HPO:probinson[2017-05-29]
OMIM:619380	Spermatogenic failure 55		HP:0003251	PMID:28548327	PCS		2/2			P	HPO:probinson[2021-07-12]
OMIM:619380	Spermatogenic failure 55		HP:0011462	PMID:28548327	PCS		2/2			C	HPO:probinson[2021-07-12]
OMIM:619380	Spermatogenic failure 55		HP:0000007	PMID:28548327	PCS					I	HPO:probinson[2021-07-12];HPO:probinson[2021-07-12]
OMIM:619380	Spermatogenic failure 55		HP:0012207	PMID:28548327	PCS		2/2			P	HPO:probinson[2021-07-12]
OMIM:201710	Lipoid congenital adrenal hyperplasia		HP:0000007	OMIM:201710	IEA					I	HPO:iea[2009-02-17]
OMIM:201710	Lipoid congenital adrenal hyperplasia		HP:0008258	OMIM:201710	IEA					P	HPO:skoehler[2015-01-27]
OMIM:201710	Lipoid congenital adrenal hyperplasia		HP:0000840	OMIM:201710	IEA					P	HPO:iea[2009-02-17]
OMIM:201710	Lipoid congenital adrenal hyperplasia		HP:0000047	OMIM:201710	IEA					P	HPO:iea[2009-02-17]
OMIM:201710	Lipoid congenital adrenal hyperplasia		HP:0000127	OMIM:201710	IEA					P	HPO:iea[2009-02-17]
OMIM:615592	Immunodeficiency 15		HP:0004313	PMID:24369075	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0004432	PMID:24369075	PCS		3/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0003593	PMID:24369075	PCS		4/4			C	HPO:skoehler[2014-02-06];HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0009098	PMID:24369075	PCS		4/4			P	HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0012311	PMID:24369075	PCS		2/4			P	HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0031381	PMID:24369075	PCS		2/4			P	HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0001508	PMID:24369075	PCS		3/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0002719	PMID:24369075	PCS		4/4			P	HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0000007	PMID:24369075	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0001522	PMID:24369075	PCS		2/4			C	HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0002028	PMID:24369075	PCS					P	HPO:skoehler[2014-02-06];HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0002721	PMID:24369075	PCS					P	HPO:skoehler[2015-01-26];HPO:probinson[2023-01-21]
OMIM:615592	Immunodeficiency 15		HP:0040218	PMID:24369075	PCS		3/4			P	HPO:probinson[2023-01-21]
OMIM:607196	Microcephaly, Amish type		HP:0008936	PMID:20583149	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0001320	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0000340	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0003577	OMIM:607196	TAS					C	HPO:skoehler[2012-10-17]
OMIM:607196	Microcephaly, Amish type		HP:0001321	OMIM:607196	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607196	Microcephaly, Amish type		HP:0001371	OMIM:607196	TAS					P	HPO:skoehler[2012-11-21]
OMIM:607196	Microcephaly, Amish type		HP:0002033	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0002240	OMIM:607196	TAS					P	HPO:skoehler[2012-11-21]
OMIM:607196	Microcephaly, Amish type		HP:0001508	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0034198	PMID:20583149	PCS		1/1			C	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0000737	PMID:20583149	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0100704	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0011451	PMID:12185364;PMID:20583149	PCS		11/11			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0002509	PMID:20583149	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0007750	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0001338	PMID:20583149	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0000007	PMID:12185364	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0000648	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0000237	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0000347	OMIM:607196	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607196	Microcephaly, Amish type		HP:0001336	PMID:20583149	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:607196	Microcephaly, Amish type		HP:0003128	PMID:20583149	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-25]
OMIM:120000	Coarctation of aorta		HP:0001680	OMIM:120000	IEA					P	HPO:iea[2009-02-17]
OMIM:120000	Coarctation of aorta		HP:0004383	OMIM:120000	IEA					P	HPO:iea[2009-02-17]
OMIM:120000	Coarctation of aorta		HP:0001426	OMIM:120000	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:120000	Coarctation of aorta		HP:0000006	OMIM:120000	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0000473	PMID:25039795	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0012760	PMID:25039795	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0010819	PMID:25039795	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0001263	PMID:25039795;PMID:17847003	PCS		7/8			P	HPO:probinson[2023-02-11];HPO:skoehler[2015-04-05];HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0003593	PMID:25039795	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0002174	PMID:25039795	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0030186	PMID:25039795	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0000007	PMID:17847003	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0001249	PMID:25039795;PMID:17847003	PCS		7/8			P	HPO:probinson[2023-02-11];HPO:probinson[2013-04-01];HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0004305	PMID:25039795	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-11]
OMIM:611092	Intellectual developmental disorder, autosomal recessive 6		HP:0001336	PMID:25039795	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-11]
OMIM:618908	Silver-Russell syndrome 5		HP:0002750	PMID:29655892	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0003561	PMID:28796236	IEA	HP:0003577	2/2			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0003561	PMID:29655892	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0001518	PMID:28796236	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0001518	PMID:29655892	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0011220	PMID:28796236;PMID:29655892	PCS		3/3			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0004482	PMID:28796236	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0008872	PMID:28796236	PCS	HP:0003593	2/2			P	HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0001511	PMID:28796236	PCS	HP:0030674	2/2			P	HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0000006	PMID:28796236	TAS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618908	Silver-Russell syndrome 5		HP:0000325	PMID:28796236;PMID:29655892	PCS		3/3			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001276	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000164	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000365	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000486	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0002188	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000463	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001250	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001252	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0002162	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000283	OMIM:179613	TAS					P	HPO:skoehler[2015-10-05]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001290	OMIM:179613	TAS					P	HPO:skoehler[2017-07-13]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001629	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000316	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000219	OMIM:179613	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0002119	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0008897	OMIM:179613	TAS					P	HPO:skoehler[2012-10-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0002714	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000119	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001643	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000212	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001642	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000179	OMIM:179613	TAS					P	HPO:skoehler[2012-10-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000358	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001249	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0002059	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0002650	OMIM:179613	IEA					P	HPO:skoehler[2010-06-20]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001263	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000272	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0005484	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0011800	OMIM:179613	TAS					P	HPO:skoehler[2013-11-28]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0005280	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0012385	OMIM:179613	TAS					P	HPO:skoehler[2013-10-22]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0100876	OMIM:179613	TAS					P	HPO:skoehler[2012-10-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0009473	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001719	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000767	OMIM:179613	IEA					P	HPO:skoehler[2010-06-20]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001636	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0004209	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001510	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0001631	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000006	OMIM:179613	IEA					I	HPO:skoehler[2010-06-19]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000028	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000248	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000347	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000369	OMIM:179613	IEA					P	HPO:iea[2009-02-17]
OMIM:179613	Recombinant chromosome 8 syndrome		HP:0000126	OMIM:179613	IEA					P	HPO:skoehler[2010-06-18]
OMIM:169400	Pelger-Huet anomaly		HP:0002069	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000164	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000486	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001250	PMID:14684694	PCS		2/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0010047	PMID:12118250;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0010442	OMIM:169400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:169400	Pelger-Huet anomaly		HP:0001629	PMID:12118250	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001508	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0011220	OMIM:169400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:169400	Pelger-Huet anomaly		HP:0002916	PMID:16007606;PMID:19468205	PCS		HP:0040281			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000316	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0009027	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001902	PMID:10457411	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0006895	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000256	PMID:14684694	PCS		2/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000212	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001249	PMID:16007606;PMID:14684694	PCS		4/12			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0003502	PMID:14684694	PCS		2/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0009824	PMID:10457411;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001761	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0002395	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001263	OMIM:169400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:169400	Pelger-Huet anomaly		HP:0005280	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0011447	OMIM:169400	TAS					P	HPO:skoehler[2015-01-21]
OMIM:169400	Pelger-Huet anomaly		HP:0010041	PMID:12118250;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0010044	PMID:12118250;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0009099	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0002808	PMID:10457411;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001537	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000403	PMID:16007606	PCS		1/1			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000964	PMID:10457411;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0002007	PMID:16007606;PMID:12118250	PCS		2/2			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001874	PMID:16007606;PMID:19468205	PCS		HP:0040280			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001873	PMID:10457411;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0000006	PMID:16007606;PMID:19468205	PCS					I	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:169400	Pelger-Huet anomaly		HP:0001875	PMID:10457411;PMID:14684694	PCS		1/11			P	ZFIN:bruef[2012-04-24]; HPO:sdoelken[2012-04-24]
OMIM:613685	Deafness, autosomal recessive 83		HP:0000007	PMID:19888295	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-09]
OMIM:613685	Deafness, autosomal recessive 83		HP:0000399	PMID:19888295	PCS					P	HP:probinson[2019-03-09]
OMIM:124500	Vohwinkel syndrome		HP:0000365	PMID:8673107	PCS		0/45			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-02]
OMIM:124500	Vohwinkel syndrome		HP:0007460	PMID:8673107	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:124500	Vohwinkel syndrome		HP:0011463	PMID:8673107	PCS					C	HPO:probinson[2021-05-02]
OMIM:124500	Vohwinkel syndrome		HP:0009775	PMID:8673107	PCS					P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-02]
OMIM:124500	Vohwinkel syndrome		HP:0032541	PMID:8673107	PCS					P	HPO:probinson[2021-05-02]
OMIM:124500	Vohwinkel syndrome		HP:0007465	PMID:8673107	PCS		45/45			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-02]
OMIM:124500	Vohwinkel syndrome		HP:0000006	PMID:8673107	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-05-02]
OMIM:217600	Corneal dystrophy, Central type		HP:0001131	OMIM:217600	IEA					P	HPO:skoehler[2015-01-19]
OMIM:217600	Corneal dystrophy, Central type		HP:0007881	OMIM:217600	IEA					P	HPO:iea[2009-02-17]
OMIM:217600	Corneal dystrophy, Central type		HP:0000007	OMIM:217600	IEA					I	HPO:iea[2009-02-17]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000244	OMIM:613849	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000684	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000365	PMID:20579626	PCS		0/1			P	HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0004322	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000160	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0003593	PMID:20579626	PCS		2/2			C	HPO:probinson[2022-11-06];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0040160	PMID:20579626	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0001270	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000939	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0011220	PMID:20579626	PCS		1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0002979	PMID:20579626	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0030680	OMIM:613849	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0002757	PMID:20579626	PCS	HP:0003593	1/1			P	HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000218	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000336	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0001187	PMID:20579626	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0002650	PMID:20579626	PCS		1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0005620	PMID:20579626	PCS		1/1			P	HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000592	PMID:20579626	PCS		0/1			P	HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000591	PMID:20579626	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0011800	PMID:20579626	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0005280	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000007	PMID:20579626	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000703	PMID:20579626	PCS		0/1			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0006487	PMID:20579626	PCS		1/1			P	HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000768	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0006488	PMID:20579626	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0002645	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000347	PMID:20579626	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613849	Osteogenesis imperfecta, type XII		HP:0000324	PMID:20579626	PCS		1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2024-03-14]
OMIM:213300	Joubert syndrome 1		HP:0000286	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0002421	PMID:29230161	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0000486	PMID:29230161	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0010808	OMIM:213300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:213300	Joubert syndrome 1		HP:0001252	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0001251	PMID:29230161;PMID:19668216	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0001290	PMID:29230161;PMID:19668216	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0011933	OMIM:213300	TAS					P	HPO:probinson[2012-06-10]
OMIM:213300	Joubert syndrome 1		HP:0000718	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0011220	OMIM:213300	PCS					P	HPO:probinson[2012-04-01]
OMIM:213300	Joubert syndrome 1		HP:0002419	PMID:19668216	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0025336	PMID:29230161	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0000752	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000158	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0002335	OMIM:213300	TAS					P	HPO:probinson[2012-06-10]
OMIM:213300	Joubert syndrome 1		HP:0001249	PMID:19668216	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0000556	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0002553	OMIM:213300	PCS					P	HPO:probinson[2012-04-01]
OMIM:213300	Joubert syndrome 1		HP:0000252	PMID:19668216	PCS		1/7			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0002871	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000570	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0002195	OMIM:213300	TAS					P	HPO:probinson[2012-06-10]
OMIM:213300	Joubert syndrome 1		HP:0001263	PMID:29230161;PMID:19668216	PCS		8/8			P	HPO:probinson[2012-04-01];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0002790	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0007271	OMIM:213300	PCS		HP:0040283			P	HPO:probinson[2012-04-01]
OMIM:213300	Joubert syndrome 1		HP:0002508	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000007	PMID:19668216	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0000567	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000369	PMID:29230161	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0000463	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0002365	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0001395	PMID:19668216	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0010828	OMIM:213300	TAS					P	HPO:skoehler[2013-05-31]
OMIM:213300	Joubert syndrome 1		HP:0000617	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000657	PMID:19668216	PCS		7/7			P	HPO:probinson[2012-04-01];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0030084	PMID:29230161	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0002876	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000256	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0001320	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000750	PMID:29230161	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0000112	PMID:29230161	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0031936	PMID:29230161	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0001162	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0100951	OMIM:213300	PCS					P	HPO:probinson[2012-04-01]
OMIM:213300	Joubert syndrome 1		HP:0000508	PMID:29230161	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0007772	OMIM:213300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:213300	Joubert syndrome 1		HP:0000107	OMIM:213300	PCS		HP:0040283			P	HPO:probinson[2012-04-01]
OMIM:213300	Joubert syndrome 1		HP:0007973	OMIM:213300	PCS		HP:0040283			P	HPO:probinson[2012-04-01]
OMIM:213300	Joubert syndrome 1		HP:0000543	PMID:19668216	PCS		1/7			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0001357	PMID:19668216	PCS		1/7			P	HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0001830	OMIM:213300	TAS		HP:0040283			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:213300	Joubert syndrome 1		HP:0000588	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0000742	OMIM:213300	IEA					P	HPO:iea[2009-02-17]
OMIM:213300	Joubert syndrome 1		HP:0200096	OMIM:213300	TAS					P	HPO:skoehler[2013-06-04]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0001662	OMIM:611938	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0001250	OMIM:611938	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0011463	PMID:16908766	PCS		2/2			C	HPO:probinson[2022-07-12]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0000007	PMID:11704930	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-12]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0001279	PMID:16908766	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-12]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0031677	PMID:16908766	PCS		2/2		HP:0025377	P	HPO:probinson[2022-07-12]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0004756	OMIM:611938	IEA					P	HPO:skoehler[2015-01-19]
OMIM:611938	Ventricular tachycardia, catecholaminergic polymorphic, 2		HP:0001699	OMIM:611938	TAS					P	HPO:skoehler[2012-10-17]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0002069	PMID:23708187	PCS		1/1			P	HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0000252	OMIM:617391	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0001344	OMIM:617391	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0002353	PMID:23708187	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0002376	PMID:23708187	PCS		1/1			P	HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0001250	OMIM:617391	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0010819	PMID:23708187	PCS		1/1			P	HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0001263	PMID:23708187	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0003593	PMID:23708187	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0012448	OMIM:617391	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0001290	OMIM:617391	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0031475	PMID:23708187	PCS		1/1			P	HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0007270	PMID:23708187	PCS		1/1			P	HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0032792	PMID:23708187	PCS		1/1			P	HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0200134	OMIM:617391	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0002119	OMIM:617391	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0000006	PMID:23708187	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0001249	PMID:23708187	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-28]
OMIM:617391	Epileptic encephalopathy, early infantile, 54		HP:0001336	PMID:23708187	PCS		1/1			P	HPO:probinson[2022-11-28]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0002069	PMID:26370147	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0000750	PMID:26370147	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0002033	PMID:26370147	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0011463	PMID:26370147	PCS		2/2			C	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0000717	PMID:26370147	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0000403	PMID:26370147	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0001417	PMID:26370147	PCS					I	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0011003	PMID:26370147	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0000752	PMID:26370147	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:301076	Intellectual developmental disorder, X-linked, syndromic, Pilorge type		HP:0000732	PMID:26370147	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0000044	PMID:19079066	IEA					P	HPO:probinson[2013-02-26]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0000054	OMIM:614840	TAS					P	HPO:skoehler[2013-11-18]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0008197	PMID:19079066	IEA					P	HPO:probinson[2013-02-26]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0000007	PMID:19079066	IEA					I	HPO:probinson[2013-01-09]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0030260	OMIM:614840	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0008734	OMIM:614840	TAS					P	HPO:skoehler[2013-11-18]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0000028	OMIM:614840	TAS					P	HPO:skoehler[2013-11-18]
OMIM:614840	Hypogonadotropic hypogonadism 11 with or without anosmia		HP:0000786	OMIM:614840	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0002389	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001671	OMIM:615009	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001176	OMIM:615009	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000486	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001195	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001250	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0002580	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001290	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000639	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000319	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000718	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000316	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001647	OMIM:615009	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000414	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000219	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0002714	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0006610	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001643	OMIM:615009	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001763	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0002019	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001249	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000699	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0002553	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000154	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000494	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000750	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001344	OMIM:615009	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001321	OMIM:615009	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0011968	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001263	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000294	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0011098	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000508	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001833	OMIM:615009	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000527	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000664	PMID:23159249	PCS				HP:0012825	P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000400	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000006	PMID:23159249	PCS					I	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000369	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000028	PMID:23159249	PCS					P	HPO:probinson[2015-05-10]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0000545	OMIM:615009	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615009	Schuurs-Hoeijmakers syndrome		HP:0001655	OMIM:615009	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616500	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3		HP:0003577	PMID:21457908	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:616500	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3		HP:0001639	PMID:21457908	PCS		2/2			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-11-08]
OMIM:616500	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3		HP:0031320	PMID:21457908	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:616500	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3		HP:0000007	PMID:21457908	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:616500	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3		HP:0008347	PMID:21457908	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:606713	Van der woude syndrome 2		HP:0000175	PMID:24360809	PCS		22/27			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-10]
OMIM:606713	Van der woude syndrome 2		HP:0003577	PMID:24360809	PCS		27/27			C	HPO:probinson[2022-12-10]
OMIM:606713	Van der woude syndrome 2		HP:0000668	PMID:24360809	PCS		1/27			P	HPO:probinson[2022-12-10];HPO:probinson[2022-12-10]
OMIM:606713	Van der woude syndrome 2		HP:0000689	PMID:24360809	PCS		2/27			P	HPO:probinson[2022-12-10]
OMIM:606713	Van der woude syndrome 2		HP:0000674	PMID:24360809	PCS		1/27			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-10]
OMIM:606713	Van der woude syndrome 2		HP:0100267	PMID:24360809	PCS		14/27			P	HPO:probinson[2022-12-10]
OMIM:606713	Van der woude syndrome 2		HP:0000006	PMID:24360809	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-10]
OMIM:606713	Van der woude syndrome 2		HP:0000204	PMID:24360809	PCS		15/27			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-10]
OMIM:262710	Pituitary dwarfism with large sella turcica		HP:0000839	OMIM:262710	IEA					P	HPO:iea[2009-02-17]
OMIM:262710	Pituitary dwarfism with large sella turcica		HP:0002690	OMIM:262710	IEA					P	HPO:iea[2009-02-17]
OMIM:262710	Pituitary dwarfism with large sella turcica		HP:0000007	OMIM:262710	IEA					I	HPO:iea[2009-02-17]
OMIM:262710	Pituitary dwarfism with large sella turcica		HP:0000821	OMIM:262710	IEA					P	HPO:iea[2009-02-17]
OMIM:262710	Pituitary dwarfism with large sella turcica		HP:0000824	OMIM:262710	TAS					P	HPO:iea[2015-04-18]
OMIM:262710	Pituitary dwarfism with large sella turcica		HP:0001510	OMIM:262710	IEA					P	HPO:iea[2009-02-17]
OMIM:619155	Nephrotic syndrome, type 22		HP:0003774	PMID:33523862	PCS	HP:0003621	1/1			P	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0000100	PMID:33523862	PCS		2/2			P	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0002907	PMID:33523862	PCS		2/2			P	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0003075	PMID:33523862	PCS		2/2			P	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0003593	PMID:33523862	PCS		1/2			C	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0007430	PMID:33523862	PCS		2/2			P	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0012593	PMID:33523862	PCS		2/2			P	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0000096	PMID:33523862	PCS		1/1			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0000007	PMID:33523862	PCS					I	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0031266	PMID:33523862	PCS		1/1			P	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0003623	PMID:33523862	PCS		1/2			C	HPO:probinson[2021-02-19]
OMIM:619155	Nephrotic syndrome, type 22		HP:0004722	PMID:33523862	PCS		1/1			P	HPO:probinson[2021-02-19]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0003577	PMID:25683120	PCS		14/14			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000343	PMID:25683120	PCS		7/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000486	PMID:25683120	PCS		7/13			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000463	PMID:25683120	PCS		12/14			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000023	PMID:25683120	PCS		8/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001272	PMID:25683120	PCS		3/10			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001250	PMID:25683120	PCS		2/14			P	HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002000	PMID:25683120	PCS		14/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0003273	PMID:25683120	PCS		9/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001252	PMID:25683120	PCS		7/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002020	PMID:25683120	PCS		9/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0005272	PMID:25683120	PCS		13/14			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001270	PMID:25683120	PCS		14/14			P	HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001848	PMID:25683120	PCS		3/14			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000878	PMID:25683120	PCS		1/14			P	HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001840	PMID:25683120	PCS		1/7			P	HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002019	PMID:25683120	PCS		5/6			P	HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002059	PMID:25683120	PCS		2/10			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000494	PMID:25683120	PCS		11/13			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000750	PMID:25683120	PCS		12/12			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002650	PMID:25683120	PCS		5/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001762	PMID:25683120	PCS		10/14			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000431	PMID:25683120	PCS		14/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000293	PMID:25683120	PCS		13/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001263	PMID:25683120	PCS		11/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000470	PMID:25683120	PCS		10/12			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001181	PMID:25683120	PCS		14/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0011824	PMID:25683120	PCS		8/14			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002093	PMID:25683120	PCS		7/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0012385	PMID:25683120	PCS		14/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0006380	PMID:25683120	PCS		9/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002803	PMID:25683120	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0001537	PMID:25683120	PCS		2/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000205	PMID:25683120	PCS		9/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0009931	PMID:25683120	PCS		14/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002307	PMID:25683120	PCS		4/4			P	HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000565	PMID:25683120	PCS		2/13			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002987	PMID:25683120	PCS		7/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000006	PMID:25683120	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0000347	PMID:25683120	PCS		13/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-08-17]
OMIM:616266	Congenital contractures of the limbs and face, hypotonia, and developmental delay		HP:0002643	PMID:25683120	PCS		9/11			P	HPO:probinson[2022-08-17]
OMIM:143000	Horner syndrome, congenital		HP:0001100	OMIM:143000	IEA					P	HPO:iea[2009-02-17]
OMIM:143000	Horner syndrome, congenital		HP:0006837	OMIM:143000	IEA					P	HPO:iea[2009-02-17]
OMIM:143000	Horner syndrome, congenital		HP:0000490	OMIM:143000	IEA					P	HPO:iea[2009-02-17]
OMIM:143000	Horner syndrome, congenital		HP:0007451	OMIM:143000	IEA					P	HPO:iea[2009-02-17]
OMIM:143000	Horner syndrome, congenital		HP:0003470	OMIM:143000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:143000	Horner syndrome, congenital		HP:0000006	OMIM:143000	IEA					I	HPO:iea[2009-02-17]
OMIM:270300	Peeling skin syndrome 1		HP:0034838	OMIM:270300	TAS					P	HPO:probinson[2023-07-18]
OMIM:270300	Peeling skin syndrome 1		HP:0001880	PMID:20691404	PCS		2/2			P	HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0004322	PMID:20691404	PCS		0/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0003212	PMID:20691404	PCS		2/2			P	HPO:probinson[2012-09-18];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0002299	PMID:20691404	PCS		2/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0002099	PMID:20691404	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0040189	PMID:20691404	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0001806	PMID:20691404	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0000007	PMID:20691404	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0001019	PMID:20691404	PCS		4/4			P	HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0007410	PMID:20691404	PCS		2/4			P	HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0000989	PMID:20691404	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0008404	PMID:20691404	PCS		1/4			P	HPO:probinson[2022-10-04];HPO:probinson[2022-10-04]
OMIM:270300	Peeling skin syndrome 1		HP:0003623	PMID:20691404	PCS		4/4			C	HPO:probinson[2022-10-04]
OMIM:614465	Joubert syndrome 16		HP:0000657	PMID:22282472	PCS		8/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0000107	PMID:22282472	PCS		2/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0000316	PMID:22282472	PCS		1/12			P	HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0000007	PMID:22282472	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0000090	PMID:22282472	PCS		1/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0001305	PMID:22282472	PCS	HP:0003577	1/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0002084	PMID:22282472	PCS		1/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0002419	PMID:22282472	PCS		12/12			P	HPO:skoehler[2013-11-28];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0010442	PMID:22282472	PCS	HP:0003577	1/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0000589	PMID:22282472	PCS		6/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:614465	Joubert syndrome 16		HP:0000556	PMID:22282472	PCS		3/11			P	HPO:skoehler[2012-11-28];HPO:probinson[2020-08-09]
OMIM:609352	Epidermolysis bullosa simplex 2E, with migratory circinate erythema		HP:0031180	PMID:12925204	PCS		9/9			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:609352	Epidermolysis bullosa simplex 2E, with migratory circinate erythema		HP:0008066	PMID:12925204	PCS		9/9			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:609352	Epidermolysis bullosa simplex 2E, with migratory circinate erythema		HP:0000006	PMID:12925204	PCS					I	HPO:probinson[2022-03-27]
OMIM:609352	Epidermolysis bullosa simplex 2E, with migratory circinate erythema		HP:0033802	PMID:12925204	PCS		9/9			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:609352	Epidermolysis bullosa simplex 2E, with migratory circinate erythema		HP:0003623	PMID:12925204	PCS					C	HPO:probinson[2022-03-27]
OMIM:126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0000006	OMIM:126840	IEA					I	HPO:iea[2009-02-17]
OMIM:126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0002588	OMIM:126840	IEA					P	HPO:iea[2009-02-17]
OMIM:126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0003238	OMIM:126840	IEA					P	HPO:iea[2009-02-17]
OMIM:126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0500167	OMIM:126840	TAS					P	HPO:lccarmody[2018-12-28]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0000708	PMID:27080313	PCS					P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0003596	PMID:27080313	PCS		16/19			C	HPO:probinson[2022-08-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0002145	PMID:27080313	PCS		2/13			P	HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0001260	PMID:27080313	PCS					P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0003584	PMID:27080313	PCS		3/9			C	HPO:probinson[2022-08-13]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0007354	PMID:27080313	PCS		9/13			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0002380	PMID:27080313	PCS					P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0003690	PMID:27080313	PCS					P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0001324	PMID:27080313	PCS					P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0000006	PMID:27080313	PCS					I	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619141	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5		HP:0010546	PMID:27080313	PCS					P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0002069	PMID:29939203	PCS		79/105			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0002123	OMIM:601068	TAS					P	HPO:iea[2009-02-17]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0001351	OMIM:601068	IEA					P	HPO:iea[2009-02-17]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0003581	PMID:29939203	PCS					C	HPO:probinson[2012-04-18];HPO:probinson[2021-02-06]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0003680	OMIM:601068	TAS					C	HPO:probinson[2012-04-18]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0001340	PMID:29939203	PCS		61/71			P	HPO:probinson[2012-04-18];HPO:probinson[2021-02-06]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0010852	OMIM:601068	TAS					P	HPO:probinson[2012-04-18]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0001312	OMIM:601068;PMID:29939203	PCS		74/82			P	HPO:iea[2012-04-18];HPO:probinson[2021-02-06]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0000006	PMID:29507423	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-02-06]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0001249	OMIM:601068	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0001337	PMID:29939203	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:601068	Epilepsy, familial adult myoclonic, 1		HP:0001326	OMIM:601068	TAS					P	HPO:probinson[2012-04-18]
OMIM:274600	Pendred syndrome		HP:0025484	PMID:9398842	PCS		11/14			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:274600	Pendred syndrome		HP:0001751	OMIM:274600	IEA					P	HPO:iea[2009-02-17]
OMIM:274600	Pendred syndrome		HP:0002890	OMIM:274600	IEA					P	HPO:iea[2009-02-17]
OMIM:274600	Pendred syndrome		HP:0008554	OMIM:274600	IEA					P	HPO:iea[2009-02-17]
OMIM:274600	Pendred syndrome		HP:0000007	PMID:9398842	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:274600	Pendred syndrome		HP:0008223	OMIM:274600	IEA					P	HPO:iea[2009-02-17]
OMIM:274600	Pendred syndrome		HP:0000853	PMID:9398842	PCS		14/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:274600	Pendred syndrome		HP:0001249	OMIM:274600	IEA					P	HPO:iea[2009-02-17]
OMIM:274600	Pendred syndrome		HP:0008527	OMIM:274600	IEA	HP:0003577	15/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001232	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0006548	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001694	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001250	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002140	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001394	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0007380	PMID:17219009	PCS		8/10			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001903	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0100869	PMID:17219009	PCS		8/10			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0006574	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001901	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000214	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000434	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002138	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001342	OMIM:600376	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0030049	OMIM:600376	TAS					P	HPO:skoehler[2014-09-21]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002573	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002076	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000471	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002094	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002092	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002390	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002629	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002707	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000822	OMIM:600376	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000228	PMID:17219009	PCS		6/10			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002408	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0001217	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000524	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000227	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0030491	OMIM:600376	TAS					P	HPO:skoehler[2015-07-26]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002604	OMIM:600376;PMID:17219009	PCS		12/20			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02];HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000961	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002249	PMID:17219009	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0004406	PMID:17219009	PCS	HP:0011463	10/10			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002326	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0000006	PMID:8640225	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0006107	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:600376	Telangiectasia, hereditary hemorrhagic, type 2		HP:0002248	OMIM:600376	IEA					P	HPO:iea[2009-02-17]
OMIM:614303	Edict syndrome		HP:0000483	PMID:21996275	PCS	HP:0003621	18/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-14]
OMIM:614303	Edict syndrome		HP:0000563	PMID:21996275	PCS	HP:0003621	18/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-14]
OMIM:614303	Edict syndrome		HP:0001134	PMID:21996275	PCS	HP:0011463	18/18			P	HPO:probinson[2023-01-14]
OMIM:614303	Edict syndrome		HP:0011463	PMID:21996275	PCS		18/18			C	HPO:probinson[2023-01-14]
OMIM:614303	Edict syndrome		HP:0000482	OMIM:614303	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614303	Edict syndrome		HP:0007663	OMIM:614303	TAS					P	HPO:skoehler[2015-07-26]
OMIM:614303	Edict syndrome		HP:0000505	OMIM:614303	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614303	Edict syndrome		HP:0007676	OMIM:614303	IEA					P	HPO:skoehler[2015-08-05]
OMIM:614303	Edict syndrome		HP:0000006	PMID:21996275	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-14]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0003676	OMIM:192315	TAS					C	HPO:skoehler[2012-10-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0001297	OMIM:192315	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0002186	OMIM:192315	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0001250	PMID:17660820	PCS		9/66			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0031987	OMIM:192315	IEA					P	HPO:skoehler[2018-10-08]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0001009	OMIM:192315	TAS					P	HPO:skoehler[2013-01-22]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0002518	OMIM:192315	TAS					P	HPO:probinson[2013-11-23]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0009763	OMIM:192315	IEA					P	HPO:skoehler[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0001269	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0002910	OMIM:192315	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0001147	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0002239	PMID:27604306	PCS		9/77			P	HPO:probinson[2022-08-27]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0007009	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0003565	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000573	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0002395	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0002076	PMID:17660820	PCS		28/53			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0001260	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0200029	OMIM:192315	TAS					P	HPO:probinson[2013-11-23]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0003581	PMID:17660820	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000790	OMIM:192315	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0030880	PMID:17660820	PCS		31/73			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000093	OMIM:192315	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000708	OMIM:192315	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0040049	OMIM:192315	TAS					P	HPO:skoehler[2014-11-26]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000969	OMIM:192315	TAS					P	HPO:skoehler[2013-01-22]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000529	OMIM:192315	TAS					P	HPO:skoehler[2013-05-31]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000726	PMID:17660820	PCS		33/70			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000505	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0007017	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0000006	PMID:17660820	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0001413	OMIM:192315	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:192315	Vasculopathy, retinal, with cerebral leukodystrophy		HP:0200030	OMIM:192315	IEA					P	HPO:iea[2009-02-17]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0000750	PMID:27993705	PCS		10/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0000276	PMID:27993705	PCS		4/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0000283	PMID:27993705	PCS		6/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0001270	PMID:27993705	PCS		4/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0011463	PMID:27993705	PCS					C	HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0000729	PMID:27993705	PCS		2/11			P	HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0011220	PMID:27993705	PCS		3/11			P	HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0001417	PMID:19377476	PCS					I	HPO:probinson[2013-02-17]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0000400	PMID:27993705	PCS		4/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0000664	PMID:27993705	PCS		3/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0001513	PMID:27993705	PCS		4/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:300803	Intellectual developmental disorder, X-linked 97		HP:0001249	PMID:27993705	PCS		11/11			P	HPO:probinson[2021-09-25]
OMIM:617622	Joubert syndrome 30		HP:0003577	PMID:28625504	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0001272	PMID:28625504	PCS		2/11			P	HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0001250	PMID:28625504	PCS		2/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0001274	PMID:28625504	PCS		0/11			P	HPO:probinson[2021-06-13]
OMIM:617622	Joubert syndrome 30		HP:0001252	PMID:28625504	PCS					P	HPO:probinson[2021-06-13]
OMIM:617622	Joubert syndrome 30		HP:0002282	PMID:28625504	PCS		3/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0010442	PMID:28625504	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0001305	PMID:28625504	PCS		1/11			P	HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0002419	PMID:28625504	PCS		11/11			P	HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0007663	PMID:28625504	PCS		1/11			P	HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0000219	PMID:28625504	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0002119	PMID:28625504	PCS		3/11			P	HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0000218	PMID:28625504	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0001249	PMID:28625504	PCS		11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0000556	PMID:28625504	PCS		2/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0000054	PMID:28625504	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0000750	PMID:28625504	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-13]
OMIM:617622	Joubert syndrome 30		HP:0000431	PMID:28625504	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0000496	PMID:28625504	PCS		9/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0001162	PMID:28625504	PCS		1/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0020185	PMID:28625504	PCS		11/11			P	HPO:probinson[2021-06-13]
OMIM:617622	Joubert syndrome 30		HP:0000193	PMID:28625504	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0001263	PMID:28625504	PCS		11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0004691	PMID:28625504	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0000609	PMID:28625504	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0000508	PMID:28625504	PCS		7/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0000007	PMID:28625504	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0002789	PMID:28625504	PCS		3/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0002104	PMID:28625504	PCS		3/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-30]
OMIM:617622	Joubert syndrome 30		HP:0000589	PMID:28625504	PCS		0/8			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0000347	PMID:28625504	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:617622	Joubert syndrome 30		HP:0002126	PMID:28625504	PCS		0/11			P	HPO:probinson[2021-06-13]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001770	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001773	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0004322	PMID:35174115	PCS		1/2			P	HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0010049	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0012745	OMIM:170390	TAS					P	HPO:skoehler[2014-03-24]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000716	OMIM:170390	TAS					P	HPO:skoehler[2015-12-30]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000836	PMID:35174115	PCS		1/2			P	HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000316	PMID:35174115	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001328	OMIM:170390	TAS		HP:0040283		HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000678	PMID:35174115	PCS		2/2			P	HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001962	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000677	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000175	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000252	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0005147	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0002750	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001382	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0005184	PMID:35174115	PCS		1/2			P	HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000327	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001657	OMIM:170390	TAS					P	HPO:skoehler[2015-01-21]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0002900	OMIM:170390	IEA					P	HPO:skoehler[2019-09-07]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0004209	PMID:35174115	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000006	PMID:11371347	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000369	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000325	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000324	OMIM:170390	TAS				HP:0012825	P	HPO:probinson[2012-04-11]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0004467	OMIM:170390	TAS					P	HPO:skoehler[2012-10-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0005478	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001156	OMIM:170390	TAS					P	HPO:skoehler[2014-11-26]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000581	OMIM:170390	TAS					P	HPO:probinson[2012-04-11]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0003691	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0030033	PMID:35174115	PCS		1/2			P	HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0010743	OMIM:170390	TAS					P	HPO:probinson[2012-04-11]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001507	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0008153	OMIM:170390	TAS					P	HPO:probinson[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0006297	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000337	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000414	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000219	OMIM:170390	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000218	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0006335	OMIM:170390	TAS					P	HPO:probinson[2012-04-11]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000696	OMIM:170390	TAS					P	HPO:probinson[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0003768	PMID:35174115	PCS		2/2			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0009803	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001864	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0003621	PMID:35174115	PCS		1/2			C	HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0002650	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0004279	OMIM:170390	TAS					P	HPO:probinson[2012-04-11]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0003100	OMIM:170390	TAS					P	HPO:probinson[2012-04-11]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000272	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0025072	OMIM:170390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0025708	PMID:35174115	PCS		1/2			C	HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0003778	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0200055	PMID:35174115	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0003779	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0001279	OMIM:170390	IEA					P	HPO:iea[2009-02-17]
OMIM:170390	Andersen cardiodysrhythmic periodic paralysis		HP:0000347	PMID:35174115	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0003676	PMID:31187503	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0003621	PMID:31187503	PCS		4/5			C	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0001761	PMID:31187503	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0000551	PMID:31187503	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0003484	PMID:31187503	PCS	HP:0025708	5/5			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0001284	PMID:31187503	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0034337	PMID:31187503	PCS		3/5			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0011463	PMID:31187503	PCS		1/5			C	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0007340	PMID:31187503	PCS		5/5			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0007210	PMID:31187503	PCS		5/5			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0000007	PMID:31187503	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0007663	PMID:31187503	PCS		2/2			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0000648	PMID:31187503	PCS	HP:0003581	5/5			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0000543	PMID:31187503	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0002403	PMID:31187503	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0006886	PMID:31187503	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0001765	PMID:31187503	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-06-04]
OMIM:618511	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy		HP:0007328	PMID:31187503	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0000098	OMIM:613444	TAS					P	HPO:probinson[2024-12-27]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0000122	OMIM:613444	TAS					P	HPO:probinson[2024-12-27]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0001263	OMIM:613444	TAS					P	HPO:probinson[2024-12-27]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0002251	OMIM:613444	TAS					P	HPO:probinson[2024-12-27]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0003745	OMIM:613444	TAS					I	HPO:probinson[2024-12-27]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0001466	OMIM:613444	TAS					I	HPO:probinson[2024-12-27]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0001513	OMIM:613444	TAS					P	HPO:probinson[2024-12-27]
OMIM:613444	Chromosome 16p11.2 deletion syndrome, 220kb		HP:0000006	OMIM:613444	TAS					I	HPO:probinson[2024-12-27]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0003477	OMIM:615035	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0003376	PMID:23188110	PCS		1/2			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0000486	OMIM:615035	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0002061	PMID:23188110	PCS		2/2			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0011399	PMID:23188110	PCS		1/1			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0100543	OMIM:615035	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0000639	OMIM:615035	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0007340	PMID:23188110	PCS		2/2			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0009027	PMID:23188110	PCS		1/2			P	HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0002936	OMIM:615035	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0007663	PMID:23188110	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0001249	OMIM:615035	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0001347	PMID:23188110	PCS		2/2			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0003621	PMID:23188110	PCS		2/2			C	HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0001762	OMIM:615035	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0003487	PMID:23188110	PCS		1/2			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0001288	OMIM:615035	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0002079	OMIM:615035	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0006937	PMID:23188110	PCS		2/2			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0001263	OMIM:615035	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0003383	PMID:23188110	PCS		1/2			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0011449	PMID:23188110	PCS		1/2			P	HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0007210	PMID:23188110	PCS		2/2			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0000007	PMID:23188110	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0000648	PMID:23188110	PCS		1/1			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0000603	PMID:23188110	PCS		2/2			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0001258	PMID:23188110	PCS		2/2			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-07]
OMIM:615035	Spastic paraplegia 55, autosomal recessive		HP:0006886	PMID:23188110	PCS		2/2			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:238350	HYPERLEXIA		HP:0000717	OMIM:238350	IEA					P	HPO:iea[2009-02-17]
OMIM:238350	HYPERLEXIA		HP:0000007	OMIM:238350	IEA					I	HPO:iea[2009-02-17]
OMIM:238350	HYPERLEXIA		HP:0001426	OMIM:238350	IEA					I	HPO:iea[2009-02-17]
OMIM:238350	HYPERLEXIA		HP:0003745	OMIM:238350	IEA					I	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0003038	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0001883	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0003022	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0000160	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0000171	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0001518	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0009486	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0000954	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0000007	OMIM:227270	IEA					I	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0030680	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0009237	OMIM:227270	TAS					P	HPO:probinson[2012-06-08]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0003811	OMIM:227270	IEA					C	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0000278	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0009778	OMIM:227270	TAS					P	HPO:probinson[2012-06-08]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0000347	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:227270	Faciocardiomelic dysplasia, lethal		HP:0002984	OMIM:227270	IEA					P	HPO:iea[2009-02-17]
OMIM:275250	Tongue, pigmented fungiform papillae of		HP:0000007	OMIM:275250	IEA					I	HPO:iea[2009-02-17]
OMIM:275250	Tongue, pigmented fungiform papillae of		HP:0000157	OMIM:275250	IEA					P	HPO:iea[2009-02-17]
OMIM:611521	Immunodeficiency 35		HP:0003212	PMID:17088085	PCS					P	HPO:probinson[2013-04-06]
OMIM:611521	Immunodeficiency 35		HP:0011274	PMID:17088085	PCS					P	HPO:probinson[2013-04-06]
OMIM:611521	Immunodeficiency 35		HP:0000007	PMID:17088085	PCS					I	HPO:probinson[2013-01-09]
OMIM:611521	Immunodeficiency 35		HP:0004429	PMID:17088085	PCS					P	HPO:probinson[2013-04-06]
OMIM:611521	Immunodeficiency 35		HP:0002205	OMIM:611521	TAS					P	HPO:skoehler[2014-10-06]
OMIM:611521	Immunodeficiency 35		HP:0002841	PMID:17088085	PCS					P	HPO:probinson[2013-04-06]
OMIM:611521	Immunodeficiency 35		HP:0002721	OMIM:611521	TAS					P	HPO:skoehler[2014-10-06]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0004325	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0003213	PMID:9579555	PCS					P	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000483	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0003079	OMIM:278760	TAS					P	HPO:skoehler[2012-10-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000365	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0004322	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0002860	PMID:9579555	PCS		2/18			P	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0001371	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0001251	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0031287	OMIM:278760	IEA					P	HPO:skoehler[2018-10-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0010783	PMID:9579555	PCS		14/14			P	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0012444	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0031525	PMID:9579555	PCS		3/18			P	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000639	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0011463	PMID:9579555	PCS		4/13			C	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0002977	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0007587	OMIM:278760	IEA					P	HPO:skoehler[2010-06-20]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0001249	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000252	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0003621	PMID:9579555	PCS		9/13			C	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000992	OMIM:278760	IEA					P	HPO:skoehler[2010-06-20]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0002650	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000490	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0002011	OMIM:278760	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0002671	PMID:9579555	PCS		9/18			P	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0001480	PMID:9579555	PCS		18/18			P	HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000726	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0008069	OMIM:278760	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0000007	PMID:8797827	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0200034	OMIM:278760	IEA					P	HPO:skoehler[2010-06-20]
OMIM:278760	Xeroderma pigmentosum, complementation group F		HP:0001337	OMIM:278760	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:178900	Pupillary membrane, persistence of		HP:0009917	OMIM:178900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:178900	Pupillary membrane, persistence of		HP:0000485	OMIM:178900	IEA					P	HPO:iea[2009-02-17]
OMIM:178900	Pupillary membrane, persistence of		HP:0000519	OMIM:178900	IEA					P	HPO:iea[2009-02-17]
OMIM:178900	Pupillary membrane, persistence of		HP:0000006	OMIM:178900	IEA					I	HPO:iea[2009-02-17]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0004325	PMID:27250695;PMID:29644084	PCS		14/22			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000286	PMID:29644084	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000341	OMIM:608716	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0003577	PMID:16673149	PCS		6/6			C	HPO:probinson[2012-07-24];HPO:probinson[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000340	PMID:16673149	PCS		6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-23]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000582	PMID:29644084	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000365	OMIM:608716	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0004322	PMID:27250695;PMID:29644084	PCS		16/22			P	HPO:probinson[2012-07-24];HPO:probinson[2024-07-02];ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0001250	PMID:27250695	PCS		1/21			P	HPO:probinson[2009-02-17];HPO:probinson[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0001274	OMIM:608716	TAS					P	HPO:probinson[2012-07-24]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0001270	PMID:29644084	PCS		1/1			P	HPO:probinson[2012-07-24];HPO:probinson[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000718	PMID:27250695	PCS		3/21			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0011461	PMID:29644084	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0002539	OMIM:608716	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0002119	OMIM:608716	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000218	PMID:29644084	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000752	PMID:27250695	PCS		7/20			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0001249	PMID:16673149;PMID:27250695;PMID:29644084	PCS		24/24			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-23];ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0005469	PMID:16673149	PCS		1/6			P	HPO:probinson[2022-06-23]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0002553	OMIM:608716	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0002179	PMID:29644084	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0006956	PMID:29644084	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000252	PMID:16673149;PMID:27250695;PMID:29644084	PCS		28/28			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-23];ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000750	PMID:29644084	PCS		1/1			P	HPO:probinson[2012-07-24];HPO:probinson[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0001321	OMIM:608716	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0002079	OMIM:608716	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0002472	OMIM:608716	TAS					P	HPO:probinson[2009-02-17]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000007	PMID:12355089	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-06-23]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0100716	PMID:27250695	PCS		2/21			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0007018	OMIM:608716	TAS					P	HPO:probinson[2012-07-24]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000520	OMIM:608716	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0000347	PMID:29644084	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:608716	Microcephaly 5, primary, autosomal recessive		HP:0009879	PMID:29644084	PCS		1/1			P	HPO:probinson[2012-07-24];HPO:probinson[2024-07-02]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000286	PMID:31124279	PCS		4/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001034	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000164	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000486	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0002384	PMID:31124279	PCS		1/12			P	HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001252	PMID:31124279	PCS		8/12			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0003593	PMID:31124279	PCS					C	HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000280	PMID:31124279	PCS		6/12			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001270	PMID:31124279	PCS		10/11			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000957	PMID:31124279	PCS		2/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0011220	PMID:31124279	PCS		5/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0012471	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000752	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0002557	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000311	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001169	PMID:31124279	PCS		4/11			P	HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000577	PMID:31124279	PCS		2/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001028	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000154	PMID:31124279	PCS		2/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000750	PMID:31124279	PCS		11/11			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000293	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001382	PMID:31124279	PCS		4/11			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000193	PMID:31124279	PCS		1/12			P	HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001263	PMID:31124279	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0005280	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000506	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000729	PMID:31124279	PCS		6/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0011098	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000767	PMID:31124279	PCS		2/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000426	PMID:31124279	PCS		4/12			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0004209	PMID:31124279	PCS		2/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000268	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000565	PMID:31124279	PCS		1/12			P	HPO:skoehler[2019-09-07]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000400	PMID:31124279	PCS		6/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0001159	PMID:31124279	PCS		4/12			P	HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000006	PMID:31124279	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000028	PMID:31124279	PCS		1/8	MALE		P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:618505	Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities		HP:0000303	PMID:31124279	PCS		3/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-20]
OMIM:619828	Spermatogenic failure 70		HP:0003251	PMID:29581481	PCS		3/3			P	HPO:probinson[2022-06-19]
OMIM:619828	Spermatogenic failure 70		HP:0011462	PMID:29581481	PCS		3/3			C	HPO:probinson[2022-06-19]
OMIM:619828	Spermatogenic failure 70		HP:0000007	PMID:29581481	PCS					I	HPO:probinson[2022-06-19]
OMIM:619828	Spermatogenic failure 70		HP:0012207	PMID:29581481	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:619828	Spermatogenic failure 70		HP:0000798	PMID:29581481	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:619828	Spermatogenic failure 70		HP:0000027	PMID:29581481	PCS		2/3			P	HPO:probinson[2022-06-19]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0008936	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0002510	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000054	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000252	PMID:35861243	PCS		3/3		HP:0012827	P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0001344	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0002540	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000365	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000574	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0003593	PMID:35861243	PCS		3/3			C	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0002072	PMID:35861243	PCS		2/2			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0033454	PMID:35861243	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0011800	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000081	PMID:35861243	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0011623	PMID:35861243	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0001508	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0033142	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000007	PMID:35861243	PCS					I	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000268	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0001972	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000028	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0000347	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620071	Neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss		HP:0006844	PMID:35861243	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:300624	Fragile X syndrome		HP:0002003	PMID:25875842	PCS		3/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0001250	OMIM:300624	TAS					P	HPO:skoehler[2012-12-03]
OMIM:300624	Fragile X syndrome		HP:0000280	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0012169	PMID:25875842	PCS		4/13			P	HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0011463	PMID:29083768	PCS					C	HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0000817	PMID:25875842	PCS		8/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0007165	OMIM:300624	TAS					P	HPO:probinson[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0000717	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0003829	OMIM:300624	IEA					I	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0006099	PMID:25875842	PCS		2/13			P	HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0000752	PMID:25875842	PCS		9/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0001423	OMIM:300624	IEA					I	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0000256	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0001763	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0002457	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0002650	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0000276	PMID:25875842	PCS		5/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0003564	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0001382	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0002050	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0100023	PMID:25875842	PCS		5/13			P	HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0008640	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0000767	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0000400	PMID:25875842	PCS		6/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300624	Fragile X syndrome		HP:0001634	OMIM:300624	IEA					P	HPO:iea[2009-02-17]
OMIM:300624	Fragile X syndrome		HP:0000303	PMID:25875842	PCS		6/13			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-25]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000110	OMIM:617805	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0003577	PMID:28739660	PCS		11/11			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-05]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000076	OMIM:617805	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000130	OMIM:617805	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000085	OMIM:617805	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0003829	PMID:28739660	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-05]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000003	OMIM:617805	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000006	PMID:28739660	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-12-05]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000126	OMIM:617805	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617805	Renal hypodysplasia/aplasia 3		HP:0000104	PMID:28739660	PCS		11/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-05]
OMIM:249230	Megaepiphyseal dwarfism		HP:0000286	OMIM:249230	IEA					P	HPO:iea[2009-02-17]
OMIM:249230	Megaepiphyseal dwarfism		HP:0003510	OMIM:249230	IEA					P	HPO:skoehler[2015-01-27]
OMIM:249230	Megaepiphyseal dwarfism		HP:0000175	OMIM:249230	IEA					P	HPO:iea[2009-02-17]
OMIM:249230	Megaepiphyseal dwarfism		HP:0004322	OMIM:249230	IEA					P	HPO:iea[2009-02-17]
OMIM:249230	Megaepiphyseal dwarfism		HP:0000924	OMIM:249230	IEA					P	HPO:iea[2009-02-17]
OMIM:249230	Megaepiphyseal dwarfism		HP:0008494	OMIM:249230	IEA					P	HPO:iea[2009-02-17]
OMIM:249230	Megaepiphyseal dwarfism		HP:0001999	OMIM:249230	IEA					P	HPO:iea[2009-02-17]
OMIM:249230	Megaepiphyseal dwarfism		HP:0000007	OMIM:249230	IEA					I	HPO:iea[2009-02-17]
OMIM:125420	Dentin dysplasia, type II		HP:0033790	PMID:12354781	PCS		1/1			P	HPO:probinson[2023-04-09]
OMIM:125420	Dentin dysplasia, type II		HP:0003771	OMIM:125420	TAS					P	HPO:skoehler[2009-02-17]
OMIM:125420	Dentin dysplasia, type II		HP:0003593	PMID:12354781	PCS		7/7			C	HPO:probinson[2023-04-09]
OMIM:125420	Dentin dysplasia, type II		HP:0011060	PMID:12354781	PCS		7/7			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-04-09]
OMIM:125420	Dentin dysplasia, type II		HP:0000006	PMID:12354781	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-04-09]
OMIM:615974	Deafness, autosomal recessive 102		HP:0003577	OMIM:615974	TAS					C	HPO:skoehler[2015-12-30]
OMIM:615974	Deafness, autosomal recessive 102		HP:0000007	PMID:24741995	PCS					I	HPO:probinson[2015-05-10]
OMIM:615974	Deafness, autosomal recessive 102		HP:0012715	PMID:24741995	PCS					P	HPO:probinson[2015-05-10]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0003510	PMID:18554279	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0002650	PMID:18554279	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0010627	PMID:18554279	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0011463	PMID:18554279	PCS		1/1			C	HPO:probinson[2023-03-07]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0000839	OMIM:173100	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0030353	PMID:18554279	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0000824	PMID:18554279	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:173100	Isolated growth hormone deficiency, type II		HP:0000006	PMID:18554279	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-03-07]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0002344	PMID:30737337	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0003477	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0000365	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0001332	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0012707	PMID:30737337	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0002151	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0001251	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0001270	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0011476	PMID:28887846	PCS	HP:0003593	2/2			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0100543	PMID:28887846	PCS		2/2			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0000529	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0000407	PMID:30737337	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0000007	PMID:28887846	PCS					I	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0007256	PMID:31116475;PMID:30737337	PCS		2/2			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0007103	PMID:28887846	PCS		2/2			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0002415	PMID:30737337	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619196	Deafness, congenital, and adult-onset progressive leukoencephalopathy		HP:0001268	PMID:31116475	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:619182	Gastric adenocarcinoma and proximal polyposis of the stomach		HP:0033770	PMID:27087319;PMID:27343414	PCS		17/32			P	HPO:probinson[2021-04-30]
OMIM:619182	Gastric adenocarcinoma and proximal polyposis of the stomach		HP:0002249	PMID:27343414	PCS		1/5			P	HPO:probinson[2021-04-30]
OMIM:619182	Gastric adenocarcinoma and proximal polyposis of the stomach		HP:0000006	PMID:27087319	PCS					I	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619182	Gastric adenocarcinoma and proximal polyposis of the stomach		HP:0033769	PMID:27087319;PMID:27343414	PCS		32/32			P	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619182	Gastric adenocarcinoma and proximal polyposis of the stomach		HP:0002027	PMID:27343414	PCS		2/5			P	HPO:probinson[2021-04-30]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0000175	PMID:32631816;PMID:30791088	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0003577	PMID:30791088	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001332	PMID:32631816	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0030674	PMID:32631816	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001263	PMID:32631816	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0410030	PMID:32631816;PMID:30791088	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0000280	PMID:32631816	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001171	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0010953	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001629	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0033132	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0009473	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0000007	PMID:30791088	PCS					I	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001769	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001334	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001169	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0001631	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0000003	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0000127	PMID:32631816	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:620703	Yuksel-Vogel-Bauser syndrome		HP:0000126	PMID:32631816;PMID:30791088	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0001320	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000486	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000750	OMIM:615960	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0002198	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0001252	OMIM:615960	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0002350	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0001290	OMIM:615960	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0002282	OMIM:615960	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0001270	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0030329	PMID:25105227	PCS					P	HPO:probinson[2015-04-19]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000639	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0007033	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0003828	OMIM:615960	TAS					M	HPO:skoehler[2015-12-30]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000646	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000657	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0002518	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000007	OMIM:615960	TAS					I	HPO:skoehler[2015-04-19]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000545	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0000556	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615960	Poretti-Boltshauser syndrome		HP:0001105	OMIM:615960	TAS					P	HPO:skoehler[2014-10-06]
OMIM:240200	Hypoadrenocorticism, familial		HP:0001000	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0002013	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0001250	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0002153	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0002902	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0000007	OMIM:240200	IEA					I	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0001943	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0008872	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0000835	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0000846	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0001626	OMIM:240200	IEA					P	HPO:iea[2009-02-17]
OMIM:240200	Hypoadrenocorticism, familial		HP:0000961	OMIM:240200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:240200	Hypoadrenocorticism, familial		HP:0002104	OMIM:240200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:209600	Atrioventricular dissociation		HP:0004752	OMIM:209600	IEA					P	HPO:iea[2009-02-17]
OMIM:209600	Atrioventricular dissociation		HP:0000007	OMIM:209600	IEA					I	HPO:iea[2009-02-17]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0000750	PMID:35907405	PCS		5/10			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0031936	PMID:35907405	PCS		3/7			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0000540	PMID:35907405	PCS		1/10			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0001250	PMID:35907405	PCS		2/9			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0001382	PMID:35907405	PCS		4/8			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0001263	PMID:35907405	PCS		9/10			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0001252	PMID:35907405	PCS		4/9			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0032388	PMID:35907405	PCS		1/5			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0000729	PMID:35907405	PCS		4/9			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0000733	PMID:35907405	PCS		2/8			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0025502	PMID:35907405	PCS		4/9			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0025336	PMID:35907405	PCS		4/7			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0007018	PMID:35907405	PCS		4/9			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0000256	PMID:35907405	PCS		4/6			P	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0000006	PMID:35907405	PCS					I	HPO:probinson[2022-11-26]
OMIM:620065	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders		HP:0001249	PMID:35907405	PCS		5/10			P	HPO:probinson[2022-11-26]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003554	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0010628	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000486	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003473	OMIM:608931	TAS		20/20		HP:0012837	P	HPO:probinson[2012-07-16];HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003199	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0001252	OMIM:608931	TAS					P	HPO:probinson[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003394	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003593	OMIM:608931	IEA					C	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0001290	OMIM:608931	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0001270	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003391	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0011463	PMID:8957026	PCS		1/1			C	HPO:probinson[2022-10-01]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003828	OMIM:608931	IEA					M	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000218	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000597	PMID:8957026	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003403	PMID:8957026	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003202	OMIM:608931	TAS					P	HPO:skoehler[2015-05-31]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0002015	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000276	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003388	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003443	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0011968	OMIM:608931	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0001260	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0003680	OMIM:608931	IEA					C	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000508	PMID:8957026	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000007	PMID:8957026	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000689	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0001558	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0002804	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0002747	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0000303	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:608931	Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency		HP:0001612	OMIM:608931	IEA					P	HPO:iea[2009-02-17]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0002179	PMID:27164704	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0008936	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0002421	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0000252	PMID:27164704	PCS		1/3			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0001662	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0001250	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0011968	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0003121	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0001252	PMID:27164704	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0002020	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0012736	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0011344	PMID:27164704	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0001709	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0000007	PMID:27164704	PCS					I	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0200134	PMID:27164704	PCS	HP:0003623	3/3			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0002104	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0003623	PMID:34611970;PMID:27164704	PCS		4/4			C	HPO:probinson[2022-05-14]
OMIM:619814	Developmental and epileptic encephalopathy 101		HP:0001336	PMID:34611970	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:617839	Amyotrophic lateral sclerosis 23		HP:0002015	PMID:28469040	PCS		6/12			P	HPO:probinson[2022-04-11]
OMIM:617839	Amyotrophic lateral sclerosis 23		HP:0003596	PMID:28469040	PCS		3/12			C	HPO:probinson[2022-04-11]
OMIM:617839	Amyotrophic lateral sclerosis 23		HP:0002398	PMID:28469040	PCS					P	HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:617839	Amyotrophic lateral sclerosis 23		HP:0000726	PMID:28469040	PCS		0/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:617839	Amyotrophic lateral sclerosis 23		HP:0003584	PMID:28469040	PCS		9/12			C	HPO:probinson[2022-04-11]
OMIM:617839	Amyotrophic lateral sclerosis 23		HP:0007354	PMID:28469040	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:617839	Amyotrophic lateral sclerosis 23		HP:0000006	PMID:28469040	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-11]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001410	OMIM:616299	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002188	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001332	PMID:24341803	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001272	PMID:24341803	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0003573	OMIM:616299	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001252	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0003593	PMID:24341803	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002119	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0008358	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0003648	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001522	OMIM:616299	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002910	OMIM:616299	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0003128	OMIM:616299	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0008936	OMIM:616299	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001662	OMIM:616299	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002376	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001263	OMIM:616299	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002151	PMID:24341803	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0001285	PMID:24341803	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0025376	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002092	OMIM:616299	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002071	OMIM:616299	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0000007	PMID:24341803	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0020078	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0003217	PMID:24341803	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:616299	Lipoyltransferase 1 deficiency		HP:0002500	OMIM:616299	TAS					P	HPO:skoehler[2015-12-30]
OMIM:617187	Spermatogenic failure 16		HP:0003251	PMID:27640305	PCS		8/8			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:617187	Spermatogenic failure 16		HP:0011462	PMID:27640305	PCS		8/8			C	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:617187	Spermatogenic failure 16		HP:0000007	PMID:27640305	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617187	Spermatogenic failure 16		HP:0012207	OMIM:617187	TAS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617187	Spermatogenic failure 16		HP:0012869	OMIM:617187	TAS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000243	PMID:24997988	PCS		1/1			P	HPO:skoehler[2014-10-06]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000480	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001290	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0410030	PMID:24997988	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0032118	OMIM:615948	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0010297	OMIM:615948	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0010055	PMID:24997988	PCS		2/2			P	HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0007165	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0002419	PMID:24997988	PCS		1/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0003429	PMID:24997988	PCS		1/1			P	HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001643	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000039	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000358	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000175	PMID:24997988	PCS		1/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000252	PMID:24997988	PCS		2/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000054	PMID:24997988	PCS		2/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001344	OMIM:615948	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000695	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0002079	OMIM:615948	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001263	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0011802	PMID:24997988	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0012583	PMID:24997988	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0100258	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000007	PMID:24997988	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001338	PMID:24997988	PCS		2/2			P	HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000369	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0003577	PMID:24997988	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000582	PMID:24997988	PCS		1/1			P	HPO:skoehler[2014-10-06]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0002085	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000180	PMID:24997988	PCS		1/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001629	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001305	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0008753	PMID:24997988	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000773	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001545	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001320	PMID:24997988	PCS		2/2			P	HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001321	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001360	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001162	PMID:24997988	PCS		2/2			P	HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0011069	PMID:24997988	PCS		1/1			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-29]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000308	PMID:24997988	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000506	PMID:24997988	PCS		1/1			P	HPO:skoehler[2014-10-06]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0001631	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000028	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000347	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0002126	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0000588	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615948	Orofaciodigital syndrome XIV		HP:0009879	OMIM:615948	IEA					P	HPO:skoehler[2019-09-07]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0002563	OMIM:208250	IEA					P	HPO:iea[2009-02-17]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0011909	OMIM:208250	TAS					P	HPO:probinson[2012-06-03]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0003040	OMIM:208250	IEA					P	HPO:iea[2009-02-17]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0005186	OMIM:208250	IEA					P	HPO:iea[2009-02-17]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0005197	OMIM:208250	IEA					P	HPO:iea[2009-02-17]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0000007	OMIM:208250	IEA					I	HPO:iea[2009-02-17]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0001239	OMIM:208250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0002812	OMIM:208250	IEA					P	HPO:iea[2009-02-17]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0005194	OMIM:208250	TAS					P	HPO:probinson[2012-06-03]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0005879	OMIM:208250	IEA					P	HPO:iea[2009-02-17]
OMIM:208250	Camptodactyly-Arthropathy-Coxa vara-pericarditis syndrome		HP:0001369	OMIM:208250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:605583	Deafness, autosomal dominant 25		HP:0001751	PMID:18674745	PCS		0/23			P	HPO:probinson[2021-06-25];HPO:probinson[2024-03-10]
OMIM:605583	Deafness, autosomal dominant 25		HP:0000407	PMID:18674745	PCS		23/23			P	HPO:skoehler[2013-01-09];HPO:probinson[2021-06-25];HPO:probinson[2024-03-10]
OMIM:605583	Deafness, autosomal dominant 25		HP:0003581	PMID:18674745	PCS					C	HPO:probinson[2024-03-10]
OMIM:605583	Deafness, autosomal dominant 25		HP:0000006	PMID:18674745	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2021-06-25]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001298	PMID:27666370	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002069	PMID:27666374	PCS		2/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0003236	PMID:27666374	PCS		4/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002540	PMID:27666370	PCS		4/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000486	PMID:27666370	PCS		1/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001250	PMID:27666370	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001252	PMID:27666370	PCS	HP:0011463	5/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001252	PMID:27666374	PCS		6/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0003593	PMID:27666374	PCS		6/8			C	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001251	PMID:27666374	PCS		2/6			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002061	PMID:27666370	PCS		7/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0045075	PMID:27666370	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000639	PMID:27666370	PCS		2/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000316	PMID:27666370	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0007366	PMID:27666370	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0003429	PMID:27666370	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001324	PMID:27666374	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002019	PMID:27666370	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001249	PMID:27666370	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0003202	PMID:27666374	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000252	PMID:27666370	PCS		4/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001344	PMID:27666370	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002079	PMID:27666370	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0011968	PMID:27666370	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000490	PMID:27666370	PCS		1/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001263	PMID:27666370	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0011097	PMID:27666374	PCS		1/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002506	PMID:27666370	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000007	PMID:27666370	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000648	PMID:27666374;PMID:27666370	PCS		10/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0006986	PMID:27666370	PCS		6/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000687	PMID:27666370	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000341	PMID:27666370	PCS		1/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000582	PMID:27666370	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0003577	PMID:27666374	PCS		2/8			C	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001272	PMID:27666370	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000020	PMID:27666374	PCS		2/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0012646	PMID:27666370	PCS		2/3	MALE		P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001308	PMID:27666374	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002119	PMID:27666370	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0009765	PMID:27666370	PCS		1/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001348	PMID:27666370	PCS		6/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002650	PMID:27666370	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000750	PMID:27666370	IEA		7/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002376	PMID:27666374	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0010818	PMID:27666374	PCS		4/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0005484	PMID:27666374	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002171	PMID:27666374	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002093	PMID:27666374;PMID:27666370	PCS		6/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-04];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002607	PMID:27666374	PCS		1/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002804	PMID:27666374	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002529	PMID:27666374	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0007179	PMID:27666374	PCS		8/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001357	PMID:27666370	PCS		1/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002007	PMID:27666370	PCS		1/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000664	PMID:27666370	PCS		1/7			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0002524	PMID:27666374	PCS		1/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0001510	PMID:27666374	PCS		6/8			P	HPO:probinson[2021-05-04]
OMIM:617193	Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum		HP:0000347	PMID:27666370	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-04]
OMIM:148800	Kleeblattschaedel syndrome		HP:0000495	OMIM:148800	IEA					P	HPO:iea[2009-02-17]
OMIM:148800	Kleeblattschaedel syndrome		HP:0001363	OMIM:148800	IEA					P	HPO:iea[2009-02-17]
OMIM:148800	Kleeblattschaedel syndrome		HP:0000238	OMIM:148800	IEA					P	HPO:iea[2009-02-17]
OMIM:148800	Kleeblattschaedel syndrome		HP:0003745	OMIM:148800	IEA					I	HPO:iea[2009-02-17]
OMIM:148800	Kleeblattschaedel syndrome		HP:0000520	OMIM:148800	IEA					P	HPO:iea[2009-02-17]
OMIM:148800	Kleeblattschaedel syndrome		HP:0003070	OMIM:148800	IEA					P	HPO:iea[2009-02-17]
OMIM:148800	Kleeblattschaedel syndrome		HP:0000006	OMIM:148800	IEA					I	HPO:iea[2009-02-17]
OMIM:148800	Kleeblattschaedel syndrome		HP:0002676	OMIM:148800	IEA					P	HPO:skoehler[2015-01-27]
OMIM:611284	Dystonia, focal, task-specific		HP:0002356	OMIM:611284	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611284	Dystonia, focal, task-specific		HP:0003581	OMIM:611284	IEA					C	HPO:skoehler[2010-06-19]
OMIM:611284	Dystonia, focal, task-specific		HP:0000006	OMIM:611284	IEA					I	HPO:skoehler[2010-06-19]
OMIM:258315	Omodysplasia 1		HP:0000286	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0003038	OMIM:258315	TAS					P	HPO:probinson[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0000343	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0008905	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0001377	OMIM:258315	TAS					P	HPO:skoehler[2010-06-18]
OMIM:258315	Omodysplasia 1		HP:0000581	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0003196	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0005792	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0012107	OMIM:258315	TAS					P	HPO:skoehler[2013-08-10]
OMIM:258315	Omodysplasia 1		HP:0005050	OMIM:258315	TAS					P	HPO:probinson[2013-04-13]
OMIM:258315	Omodysplasia 1		HP:0012368	OMIM:258315	TAS					P	HPO:skoehler[2013-10-22]
OMIM:258315	Omodysplasia 1		HP:0001629	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0008873	OMIM:258315	TAS					P	HPO:probinson[2013-03-20]
OMIM:258315	Omodysplasia 1		HP:0006376	OMIM:258315	TAS					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0004415	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0001028	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0000431	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0005025	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0003066	OMIM:258315	TAS					P	HPO:skoehler[2010-06-18]
OMIM:258315	Omodysplasia 1		HP:0000272	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0000470	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0045025	OMIM:258315	IEA					P	HPO:skoehler[2018-10-08]
OMIM:258315	Omodysplasia 1		HP:0005085	OMIM:258315	TAS					P	HPO:skoehler[2015-04-05]
OMIM:258315	Omodysplasia 1		HP:0001060	OMIM:258315	TAS					P	HPO:probinson[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0005280	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0005060	OMIM:258315	TAS					P	HPO:skoehler[2015-04-05]
OMIM:258315	Omodysplasia 1		HP:0001537	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0000007	OMIM:258315	IEA					I	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0006389	OMIM:258315	TAS					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0002007	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0008800	OMIM:258315	TAS					P	HPO:probinson[2012-07-19]
OMIM:258315	Omodysplasia 1		HP:0001631	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0005736	OMIM:258315	TAS					P	HPO:probinson[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0009756	OMIM:258315	TAS					P	HPO:iea[2012-07-19]
OMIM:258315	Omodysplasia 1		HP:0000028	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:258315	Omodysplasia 1		HP:0000347	OMIM:258315	IEA					P	HPO:iea[2009-02-17]
OMIM:612955	Long QT syndrome 12		HP:0001663	OMIM:612955	TAS					P	HPO:skoehler[2015-10-05]
OMIM:612955	Long QT syndrome 12		HP:0025708	PMID:18591664	PCS		1/1			C	HPO:probinson[2022-07-09]
OMIM:612955	Long QT syndrome 12		HP:0005184	PMID:18591664	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2022-07-09]
OMIM:612955	Long QT syndrome 12		HP:0001279	PMID:18591664	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2022-07-09]
OMIM:612955	Long QT syndrome 12		HP:0001664	PMID:10220144	PCS					P	HPO:probinson[2013-04-07]
OMIM:612955	Long QT syndrome 12		HP:0000006	PMID:18591664	PCS					I	HPO:probinson[2013-04-07]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0002850	PMID:16672701	PCS		3/4			P	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0003621	PMID:16672701	PCS		2/4			C	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0030388	PMID:16672701	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0005387	PMID:16672701	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0011839	PMID:16672701	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0003593	PMID:16672701	PCS		1/4			C	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0032134	PMID:16672701	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0011108	PMID:16672701	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0032139	PMID:16672701	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0010975	PMID:16672701	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0011463	PMID:16672701	PCS		1/4			C	HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0000509	PMID:16672701	PCS		1/4		HP:0031796	P	HPO:skoehler[2013-05-31];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0002718	PMID:16672701	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0000007	PMID:16672701	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0000403	PMID:16672701	PCS		4/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0002205	PMID:16672701	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:613493	Immunodeficiency, common variable, 3		HP:0002720	PMID:16672701	PCS		3/4			P	HPO:probinson[2021-05-09]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0001572	PMID:18184143	PCS		4/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0008391	PMID:18184143	PCS		4/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0100840	PMID:18184143	PCS		4/4			P	HPO:skoehler[2013-06-05];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0040079	PMID:18184143	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0002209	PMID:18184143	PCS		4/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0000007	PMID:18184143	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0200102	PMID:18184143	PCS		4/4			P	HPO:skoehler[2013-06-05];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0000966	PMID:18184143	PCS		0/4			P	HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0001810	PMID:18184143	PCS		4/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2024-03-10]
OMIM:602401	Ectodermal dysplasia 8, Hair/tooth/nail type		HP:0006349	PMID:18184143	PCS		4/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2024-03-10]
OMIM:618459	Immunodeficiency 62		HP:0002850	PMID:30521495	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0003621	PMID:30521495	PCS		2/2			C	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0002783	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0002110	PMID:30521495	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0005353	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0410295	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0030374	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0010976	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0032139	PMID:30521495	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0000007	PMID:30521495	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0030381	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0001973	PMID:30521495	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0002788	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0005428	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:618459	Immunodeficiency 62		HP:0004315	PMID:30521495	PCS		2/2			P	HPO:probinson[2022-10-23]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0003621	PMID:35044787	PCS					C	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0001663	PMID:35044787	PCS					P	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0011462	PMID:35044787	PCS					C	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0000007	PMID:35044787	PCS					I	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0001635	PMID:35044787	PCS		5/5			P	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0033534	PMID:35044787	PCS					P	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0033755	PMID:35044787	PCS					P	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0004756	PMID:35044787	PCS					P	HPO:probinson[2022-05-09];HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0012666	PMID:35044787	PCS					P	HPO:probinson[2022-05-09]
OMIM:619747	Cardiomyopathy, dilated, 2F		HP:0001644	PMID:35044787	PCS		5/5			P	HPO:probinson[2022-05-09]
OMIM:174900	Juvenile polyposis syndrome		HP:0002014	ISBN-10:0-19-262896-8	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0002576	OMIM:174900	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0002573	ISBN-10:0-19-262896-8	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0002035	ISBN-10:0-19-262896-8	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0003003	ISBN-10:0-19-262896-8	PCS		20%			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0004394	OMIM:174900	PCS		HP:0040282			P	HPO:iea[2010-06-08]
OMIM:174900	Juvenile polyposis syndrome		HP:0003073	OMIM:174900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0001508	OMIM:174900	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0001903	ISBN-10:0-19-262896-8	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0006771	ISBN-10:0-19-262896-8	PCS		HP:0040283			P	HPO:iea[2010-06-08]
OMIM:174900	Juvenile polyposis syndrome		HP:0001217	OMIM:174900	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0002900	OMIM:174900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0006753	ISBN-10:0-19-262896-8	PCS		HP:0040283			P	HPO:iea[2010-06-08]
OMIM:174900	Juvenile polyposis syndrome		HP:0000006	OMIM:174900	PCS					I	HPO:iea[2009-02-17]
OMIM:174900	Juvenile polyposis syndrome		HP:0002027	ISBN-10:0-19-262896-8	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0007759	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0003651	OMIM:230650	TAS					P	HPO:skoehler[2012-11-21]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001332	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0004322	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001250	PMID:8198123	PCS		0/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-16]
OMIM:230650	GM1-gangliosidosis, type III		HP:0010729	PMID:8198123	PCS		0/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-16]
OMIM:230650	GM1-gangliosidosis, type III		HP:0002240	PMID:8198123	PCS		0/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-16]
OMIM:230650	GM1-gangliosidosis, type III		HP:0003274	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001350	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001251	PMID:8198123	PCS		1/3			P	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0000280	PMID:8198123	PCS		0/3			P	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0011463	PMID:8198123	PCS		3/3			C	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0008430	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0002119	PMID:8198123	PCS		2/3			P	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001744	PMID:8198123	PCS		0/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-16]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001347	PMID:8198123	PCS					P	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0003202	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0002650	PMID:8198123	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0000750	PMID:8198123	PCS		3/3			P	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001761	PMID:8198123	PCS		1/3			P	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001260	PMID:8198123	PCS		2/3			P	HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0002808	PMID:8198123	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0008166	PMID:8198123	PCS		3/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0000926	PMID:8198123	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0002506	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0002869	OMIM:230650	IEA					P	HPO:iea[2009-02-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0000007	PMID:8198123	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:230650	GM1-gangliosidosis, type III		HP:0001336	PMID:8198123	PCS		0/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-16]
OMIM:612160	Histiocytoma, angiomatoid fibrous, somatic		HP:0001442	PMID:15884099	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:612160	Histiocytoma, angiomatoid fibrous, somatic		HP:0012315	PMID:15884099	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:617018	Spinocerebellar ataxia 43		HP:0001265	PMID:27583304	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0000571	PMID:27583304	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0003596	PMID:27583304	PCS		4/7			C	HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0001761	PMID:27583304	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0003693	PMID:27583304	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0001260	PMID:27583304	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0002066	PMID:27583304	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0003584	PMID:27583304	PCS		3/7			C	HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0002063	PMID:27583304	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0001251	PMID:27583304	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0012514	PMID:27583304	PCS		2/7			P	HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0002172	PMID:27583304	PCS		6/7			P	HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0002070	PMID:27583304	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0030902	PMID:27583304	PCS		1/7			P	HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0000639	PMID:27583304	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0007141	PMID:27583304	PCS		6/7			P	HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0002936	PMID:27583304	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0000768	PMID:27583304	PCS		4/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0000006	PMID:27583304	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0003677	PMID:27583304	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0001337	PMID:27583304	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-31]
OMIM:617018	Spinocerebellar ataxia 43		HP:0006855	PMID:27583304	PCS		2/7			P	HPO:probinson[2021-05-31]
OMIM:600202	Dyslexia, susceptibility to, 2		HP:0010522	OMIM:600202	IEA					P	HPO:iea[2009-02-17]
OMIM:600202	Dyslexia, susceptibility to, 2		HP:0000006	OMIM:600202	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:616460	Intellectual developmental disorder, autosomal recessive 50		HP:0001100	PMID:25701870	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:616460	Intellectual developmental disorder, autosomal recessive 50		HP:0000252	PMID:25701870	PCS		2/2			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-02-11]
OMIM:616460	Intellectual developmental disorder, autosomal recessive 50		HP:0000407	PMID:25701870	PCS		1/2			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-02-11]
OMIM:616460	Intellectual developmental disorder, autosomal recessive 50		HP:0011463	PMID:25701870	PCS		2/2			C	HPO:probinson[2023-02-11]
OMIM:616460	Intellectual developmental disorder, autosomal recessive 50		HP:0000007	PMID:25701870	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
DECIPHER:15	Nf1-Microdeletion syndrome		HP:0001067	DECIPHER:15	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:15	Nf1-Microdeletion syndrome		HP:0000957	DECIPHER:15	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:15	Nf1-Microdeletion syndrome		HP:0000316	DECIPHER:15	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:15	Nf1-Microdeletion syndrome		HP:0001627	DECIPHER:15	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:15	Nf1-Microdeletion syndrome		HP:0000280	DECIPHER:15	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:15	Nf1-Microdeletion syndrome		HP:0001249	DECIPHER:15	IEA					P	HPO:skoehler[2013-05-29]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0001595	PMID:27965375	PCS		0/4			P	HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0000164	PMID:27965375	PCS		0/4			P	HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0001387	PMID:27965375	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0001805	PMID:27965375	PCS		3/4			P	HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0011463	PMID:27965375	PCS		3/4			C	HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0003593	PMID:27965375	PCS		1/4			C	HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0000007	PMID:27965375	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0000972	PMID:27965375	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-18]
OMIM:617756	Erythrokeratodermia variabilis et progressiva 5		HP:0000962	PMID:27965375	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-18]
OMIM:300977	Scholte syndrome		HP:0000286	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0002751	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0031878	OMIM:300977	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300977	Scholte syndrome		HP:0000054	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0000582	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0001773	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0000232	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0001272	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0003065	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0001290	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0001419	OMIM:300977	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0000348	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0007256	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0003758	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0008734	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0000455	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0200055	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0000268	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300977	Scholte syndrome		HP:0000456	OMIM:300977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:231200	Bernard-Soulier syndrome		HP:0000132	PMID:9616133	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0001892	PMID:9616133	PCS	HP:0003577				P	HPO:probinson[2009-02-17];HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0003577	PMID:7633430	PCS		1/1			C	HPO:probinson[2022-03-11]
OMIM:231200	Bernard-Soulier syndrome		HP:0003010	PMID:9616133	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0040185	PMID:7633430	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:231200	Bernard-Soulier syndrome		HP:0011871	PMID:7633430;PMID:9616133	PCS		11/11			P	HP:probinson[2019-04-08];HPO:probinson[2022-03-11]
OMIM:231200	Bernard-Soulier syndrome		HP:0000979	PMID:9616133	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0006298	PMID:9616133	PCS					P	HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0000007	PMID:9616133	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0001902	PMID:9616133	PCS					P	HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0004846	PMID:9616133	PCS					P	HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0000421	PMID:9616133	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0001873	PMID:9616133	PCS				HP:0012825	P	HPO:probinson[2009-02-17];HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0001873	PMID:7633430	PCS	HP:0003577	1/1			P	HPO:probinson[2022-03-11]
OMIM:231200	Bernard-Soulier syndrome		HP:0002239	PMID:9616133	PCS					P	HP:probinson[2019-04-08]
OMIM:231200	Bernard-Soulier syndrome		HP:0000225	PMID:9616133	PCS					P	HP:probinson[2019-04-08]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0001265	OMIM:613530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003236	OMIM:613530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003687	OMIM:613530	TAS		HP:0040283			P	HPO:skoehler[2013-06-03]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003560	OMIM:613530	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003828	OMIM:613530	TAS					M	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0008981	OMIM:613530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0009025	OMIM:613530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003829	OMIM:613530	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0001324	OMIM:613530	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003701	OMIM:613530	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003724	OMIM:613530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0000006	OMIM:613530	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613530	Muscular dystrophy, limb-girdle, type 1H		HP:0003677	OMIM:613530	TAS					C	HPO:skoehler[2012-10-17]
OMIM:190310	Tremor, nystagmus, and duodenal ulcer		HP:0000639	OMIM:190310	IEA					P	HPO:skoehler[2010-06-18]
OMIM:190310	Tremor, nystagmus, and duodenal ulcer		HP:0001317	OMIM:190310	IEA					P	HPO:iea[2009-02-17]
OMIM:190310	Tremor, nystagmus, and duodenal ulcer		HP:0030186	OMIM:190310	TAS					P	HPO:skoehler[2017-07-13]
OMIM:190310	Tremor, nystagmus, and duodenal ulcer		HP:0000006	OMIM:190310	IEA					I	HPO:iea[2009-02-17]
OMIM:190310	Tremor, nystagmus, and duodenal ulcer		HP:0001337	OMIM:190310	TAS					P	HPO:skoehler[2009-02-17]
OMIM:190310	Tremor, nystagmus, and duodenal ulcer		HP:0002588	OMIM:190310	IEA					P	HPO:iea[2009-02-17]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0003577	PMID:7655856	PCS					C	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-08]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0002904	OMIM:235700	TAS					P	HPO:skoehler[2013-10-06]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0001081	OMIM:235700	IEA					P	HPO:iea[2009-02-17]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0000007	PMID:7655856	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0001082	OMIM:235700	IEA					P	HPO:iea[2009-02-17]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0001923	OMIM:235700	TAS					P	HPO:skoehler[2013-10-06]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0001895	OMIM:235700	IEA					P	HPO:iea[2009-02-17]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0000952	PMID:7655856	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0001744	OMIM:235700	IEA					P	HPO:iea[2009-02-17]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:6000559	PMID:7234862	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0001897	OMIM:235700	IEA					P	HPO:iea[2009-02-17]
OMIM:235700	Hemolytic anemia, nonspherocytic, due to hexokinase deficiency		HP:0001930	PMID:7655856	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:617030	Myopathy, distal, 5		HP:0003555	PMID:26506222	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0003621	PMID:26506222	PCS		4/4			C	HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0008959	PMID:26506222	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0009053	PMID:26506222	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0003693	PMID:26506222	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0003198	PMID:26506222	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0000007	PMID:26506222	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0003805	PMID:26506222	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0030319	PMID:26506222	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0003677	PMID:26506222	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0008180	PMID:26506222	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617030	Myopathy, distal, 5		HP:0002600	PMID:26506222	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:619009	Oocyte maturation defect 8		HP:0025132	PMID:32502391	PCS		0/4			P	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29];HPO:probinson[2024-03-16]
OMIM:619009	Oocyte maturation defect 8		HP:0008222	PMID:32502391	PCS		4/4			P	HPO:probinson[2020-11-29]
OMIM:619009	Oocyte maturation defect 8		HP:0000140	PMID:32502391	PCS		0/4			P	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29];HPO:probinson[2024-03-16]
OMIM:619009	Oocyte maturation defect 8		HP:0000007	PMID:32502391	PCS					I	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619009	Oocyte maturation defect 8		HP:0033336	PMID:32502391	IEA		4/4			P	HPO:probinson[2020-12-07]
OMIM:620850	Spermatogenic failure 94		HP:0034309	PMID:38441556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0034011	PMID:38441556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0032560	PMID:38441556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0003251	PMID:38441556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0011462	PMID:38441556	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0012207	PMID:38441556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0000007	PMID:38441556	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0032558	PMID:38441556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0000798	PMID:38441556	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620850	Spermatogenic failure 94		HP:0032559	PMID:38441556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:106400	Ankylosing vertebral hyperostosis with tylosisdiffuse idiopathic skeletal hyperostosis, included		HP:0007508	OMIM:106400	IEA					P	HPO:iea[2009-02-17]
OMIM:106400	Ankylosing vertebral hyperostosis with tylosisdiffuse idiopathic skeletal hyperostosis, included		HP:0008442	OMIM:106400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:106400	Ankylosing vertebral hyperostosis with tylosisdiffuse idiopathic skeletal hyperostosis, included		HP:0000006	OMIM:106400	IEA					I	HPO:iea[2009-02-17]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001396	PMID:15235028	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0003577	PMID:15235028	PCS		1/3			C	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001410	PMID:15235028	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000343	PMID:15235028	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0002243	PMID:12480927	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0031507	PMID:15235028	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001252	PMID:15235028	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0002240	PMID:12480927	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0003593	PMID:12480927	PCS		1/1			C	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0003073	PMID:15235028;PMID:12480927	PCS		4/4			P	HPO:probinson[2022-05-14];HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0003270	PMID:15235028	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001929	PMID:12480927	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001508	PMID:15235028	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001903	PMID:15235028	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0011682	PMID:15235028	PCS		1/3			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0011461	PMID:15235028	PCS		2/3			C	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000316	PMID:15235028	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000239	PMID:15235028	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001522	PMID:15235028	PCS		2/3			C	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001643	PMID:15235028	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0002014	PMID:12480927	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001562	PMID:15235028	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0003642	PMID:12480927	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001762	PMID:15235028	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001541	PMID:15235028;PMID:12480927	PCS		3/3			P	HPO:probinson[2022-05-14];HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0002013	PMID:15235028	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000470	PMID:15235028	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0012385	PMID:15235028	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000969	PMID:15235028;PMID:12480927	PCS		4/4			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000007	PMID:12480927	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001558	PMID:15235028	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000821	PMID:15235028	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001976	PMID:12480927	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001511	PMID:15235028	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0003811	PMID:15235028	PCS		1/3			C	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0001873	PMID:15235028	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000028	PMID:15235028	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0003259	PMID:15235028	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:608104	Congenital disorder of glycosylation, type Ih		HP:0000369	PMID:15235028	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0025573	PMID:27063057	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0000662	PMID:27063057	PCS	HP:0011463	3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0000540	PMID:27063057	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0000639	PMID:27063057	PCS		0/4			P	HPO:probinson[2023-02-04]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0011463	PMID:27063057	PCS		2/4			C	HPO:probinson[2023-02-04]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0003581	PMID:27063057	PCS		2/4			C	HPO:probinson[2023-02-04]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0000613	PMID:27063057	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617024	Night blindness, congenital stationary, type 1H		HP:0000007	PMID:27063057	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0002069	PMID:37541189	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0001276	PMID:37541189	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0002188	PMID:37541189	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0001252	PMID:37541189	PCS		7/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0003593	PMID:37541189	PCS		13/13			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0010862	PMID:37541189	PCS		11/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0040082	PMID:37541189	PCS		7/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0031987	PMID:37541189	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0100034	PMID:37541189	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000319	PMID:37541189	PCS		6/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000316	PMID:37541189	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000219	PMID:37541189	PCS		10/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000311	PMID:37541189	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000252	PMID:37541189	PCS		3/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000494	PMID:37541189	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000750	PMID:37541189	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0001344	PMID:37541189	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0002870	PMID:37541189	PCS		3/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0031936	PMID:37541189	PCS		8/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0011968	PMID:37541189	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000490	PMID:37541189	PCS		7/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0001263	PMID:37541189	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0002194	PMID:37541189	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0011147	PMID:37541189	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000448	PMID:37541189	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000601	PMID:37541189	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0001511	PMID:37541189	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000248	PMID:37541189	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620688	Intellectual developmental disorder, autosomal dominant 74		HP:0000006	PMID:37541189	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0003676	PMID:30460687	PCS		1/1			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0033748	PMID:30460687	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0003596	PMID:30460687	PCS		1/1			C	HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0002067	PMID:30460687	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001332	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001310	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0002461	PMID:29910000	PCS		12/12			P	HPO:probinson[2024-02-27]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001350	PMID:29910000;PMID:30460687	PCS		7/13			P	HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001251	PMID:29910000	PCS		5/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0025041	PMID:29910000;PMID:30460687	PCS		9/13			P	HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0012444	PMID:30460687	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001268	PMID:29910000;PMID:30460687	PCS		3/13			P	HPO:probinson[2022-12-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001347	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0002135	PMID:29910000	PCS		12/12			P	HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0000571	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0002015	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001300	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0002354	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0002076	PMID:29910000	PCS		2/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001260	PMID:30460687	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0003581	PMID:29910000	PCS		12/12			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0002072	PMID:29910000	PCS		1/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0000709	OMIM:618317	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0000007	PMID:29910000	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0007256	OMIM:618317	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618317	Basal ganglia calcification, idiopathic, 7, autosomal recessive		HP:0001315	PMID:30460687	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:227310	Factor V and factor VIII, combined deficiency of, with normal proteinc and protein C inhibitor		HP:0001892	OMIM:227310	IEA					P	HPO:iea[2009-02-17]
OMIM:227310	Factor V and factor VIII, combined deficiency of, with normal proteinc and protein C inhibitor		HP:0003125	OMIM:227310	IEA					P	HPO:iea[2009-02-17]
OMIM:227310	Factor V and factor VIII, combined deficiency of, with normal proteinc and protein C inhibitor		HP:0003225	OMIM:227310	IEA					P	HPO:iea[2009-02-17]
OMIM:227310	Factor V and factor VIII, combined deficiency of, with normal proteinc and protein C inhibitor		HP:0000007	OMIM:227310	IEA					I	HPO:iea[2009-02-17]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000121	OMIM:615633	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0003026	OMIM:615633	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0001561	OMIM:615633	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000750	OMIM:615633	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0001156	OMIM:615633	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0001591	OMIM:615633	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0002093	OMIM:615633	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0100259	OMIM:615633	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000888	OMIM:615633	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000007	OMIM:615633	TAS					I	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0002205	OMIM:615633	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000774	OMIM:615633	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000510	OMIM:615633	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0006644	OMIM:615633	IEA					P	HPO:skoehler[2015-01-27]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0000028	OMIM:615633	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615633	Short-Rib thoracic dysplasia 11 with or without polydactyly		HP:0001513	OMIM:615633	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615155	Steel syndrome		HP:0001377	PMID:24986830	PCS		1/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0002650	PMID:24986830	PCS		2/2			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0000431	OMIM:615155	TAS					P	HPO:skoehler[2013-04-18]
OMIM:615155	Steel syndrome		HP:0000463	PMID:24986830	PCS		2/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0001761	PMID:24986830	PCS		0/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0004322	PMID:24986830	PCS		2/2			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0001263	OMIM:615155	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:615155	Steel syndrome		HP:0003593	PMID:24986830	PCS		1/2			C	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0011800	PMID:24986830	PCS		2/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0003083	PMID:24986830	PCS		1/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0000407	OMIM:615155	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:615155	Steel syndrome		HP:0011463	PMID:24986830	PCS		1/2			C	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0002827	PMID:24986830	PCS		2/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0011220	OMIM:615155	TAS					P	HPO:skoehler[2013-04-18]
OMIM:615155	Steel syndrome		HP:0002938	PMID:24986830	PCS		1/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0000316	OMIM:615155	TAS					P	HPO:skoehler[2013-04-18]
OMIM:615155	Steel syndrome		HP:0000007	PMID:24986830	PCS					I	HPO:skoehler[2013-04-18];HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0002812	PMID:24986830	PCS		1/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0004209	PMID:24986830	PCS		2/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0009702	PMID:24986830	PCS		2/2			P	HPO:probinson[2023-04-03]
OMIM:615155	Steel syndrome		HP:0001763	PMID:24986830	PCS		1/2			P	HPO:probinson[2023-04-03]
OMIM:186200	Syndactyly, type IV		HP:0001199	PMID:18417549	PCS					P	HPO:iea[2009-02-17]
OMIM:186200	Syndactyly, type IV		HP:0100259	OMIM:186200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:186200	Syndactyly, type IV		HP:0010708	PMID:18417549	PCS					P	HPO:iea[2009-02-17]
OMIM:186200	Syndactyly, type IV		HP:0006088	OMIM:186200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:186200	Syndactyly, type IV		HP:0005917	OMIM:18417549	PCS					P	HPO:iea[2009-02-17]
OMIM:186200	Syndactyly, type IV		HP:0004691	OMIM:186200	IEA					P	HPO:iea[2012-04-24]
OMIM:186200	Syndactyly, type IV		HP:0010442	PMID:18417549	PCS					P	HPO:iea[2009-02-17]
OMIM:186200	Syndactyly, type IV		HP:0000006	PMID:18417549	PCS					I	HPO:iea[2009-02-17]
OMIM:186200	Syndactyly, type IV		HP:0001501	OMIM:186200	TAS					P	HPO:skoehler[2012-10-17]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0003431	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0001761	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0002450	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0002495	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0010829	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0003382	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0010831	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0007328	DECIPHER:29	IEA					P	HPO:skoehler[2013-05-29]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0003521	OMIM:271630	TAS					P	HPO:skoehler[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0003301	PMID:122434	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0002751	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0007759	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0008418	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0003310	PMID:122434	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0001288	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0006607	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0000470	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0012066	OMIM:271630	TAS					P	HPO:probinson[2012-08-04]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0100864	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0002938	PMID:122434	PCS		4/4			P	HPO:probinson[2024-03-09]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0000007	PMID:122434	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0003418	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0002945	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0006413	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:271630	Brachyolmia type 1, Toledo type		HP:0008922	OMIM:271630	IEA					P	HPO:iea[2009-02-17]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0001176	OMIM:102100	PCS					P	HPO:probinson[2012-03-17]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0000098	OMIM:102100	PCS					P	HPO:probinson[2012-03-17]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0030314	OMIM:102100	TAS					P	HPO:skoehler[2015-04-05]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0001833	OMIM:102100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0000977	OMIM:102100	IEA					P	HPO:iea[2009-02-17]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0010541	OMIM:102100	PCS					P	HPO:probinson[2012-03-17]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0000006	OMIM:102100	IEA					I	HPO:iea[2009-02-17]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0000303	OMIM:102100	PCS					P	HPO:probinson[2012-03-17]
OMIM:102100	Acromegaloid changes, cutis verticis gyrata, and corneal leukoma		HP:0000478	OMIM:102100	IEA					P	HPO:iea[2009-02-17]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0002465	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000582	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001212	PMID:24916641	PCS		2/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000260	PMID:24916641	PCS		2/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0100490	PMID:24916641	PCS		2/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0010808	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001252	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0002162	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0004482	PMID:24916641	PCS		2/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001629	PMID:24916641;PMID:21826058	PCS		3/7			P	HPO:probinson[2023-05-18];HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0010055	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0100702	PMID:21826058	PCS		1/5			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0009882	OMIM:300963	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000316	PMID:24916641;PMID:21826058	PCS		14/14			P	HPO:probinson[2023-05-18];HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001845	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000337	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001305	PMID:24916641;PMID:21826058	PCS		3/7			P	HPO:probinson[2023-05-18];HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0008897	PMID:24916641	PCS		2/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000218	PMID:21826058	PCS					P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001643	OMIM:300963	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001249	PMID:24916641;PMID:21826058	PCS		5/7			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000475	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0002650	OMIM:300963	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001321	PMID:21826058	PCS		1/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0031936	PMID:24916641	PCS		2/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0004971	PMID:21826058	PCS		1/5		HP:0012833	P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001263	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0012385	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001419	PMID:21826058	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0004209	PMID:24916641	PCS		2/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000444	PMID:21826058	PCS					P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001159	OMIM:300963	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0001631	PMID:21826058	PCS		1/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000322	PMID:24916641	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000028	PMID:24916641;PMID:21826058	PCS		4/7			P	HPO:probinson[2023-05-18];HPO:skoehler[2015-12-30];HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0000501	PMID:24916641	PCS		1/2			P	HPO:probinson[2023-05-18]
OMIM:300963	Ritscher-Schinzel syndrome 2		HP:0002566	PMID:21826058	PCS		1/5			P	HPO:probinson[2023-05-18]
OMIM:609597	Parietal foramina 2		HP:0002697	OMIM:609597	IEA					P	HPO:iea[2009-02-17]
OMIM:609597	Parietal foramina 2		HP:0002697	OMIM:609597	IEA	HP:0003577	6/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-06]
OMIM:609597	Parietal foramina 2		HP:0003577	PMID:11106354	PCS		6/6			C	HPO:probinson[2022-09-06]
OMIM:609597	Parietal foramina 2		HP:0007385	OMIM:609597	IEA					P	HPO:iea[2009-02-17]
OMIM:609597	Parietal foramina 2		HP:0000316	OMIM:609597	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:609597	Parietal foramina 2		HP:0012811	OMIM:609597	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:609597	Parietal foramina 2		HP:0002084	OMIM:609597	IEA					P	HPO:iea[2009-02-17]
OMIM:609597	Parietal foramina 2		HP:0005280	OMIM:609597	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:609597	Parietal foramina 2		HP:0000006	PMID:11106354	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:617971	Methemoglobinemia, Beta type		HP:0012119	OMIM:617971	TAS					P	HPO:probinson[2021-05-07];HPO:probinson[2021-05-07]
OMIM:617971	Methemoglobinemia, Beta type		HP:0000961	OMIM:617971	TAS	HP:0003593				P	HPO:probinson[2021-05-07]
OMIM:617971	Methemoglobinemia, Beta type		HP:0000006	OMIM:617971	TAS					I	HPO:probinson[2021-05-07];HPO:probinson[2021-05-07]
OMIM:300988	Immunodeficiency 50		HP:0000010	OMIM:300988	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300988	Immunodeficiency 50		HP:0004313	OMIM:300988	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300988	Immunodeficiency 50		HP:0001419	OMIM:300988	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300988	Immunodeficiency 50		HP:0001888	OMIM:300988	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300988	Immunodeficiency 50		HP:0000964	OMIM:300988	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300988	Immunodeficiency 50		HP:0002205	OMIM:300988	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300988	Immunodeficiency 50		HP:0001875	OMIM:300988	IEA					P	HPO:skoehler[2018-10-08]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0003577	PMID:8586427;PMID:7633458	PCS		2/2			C	HPO:probinson[2022-05-11]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0003819	PMID:8586427	PCS		1/1			C	HPO:probinson[2022-05-11]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0003341	PMID:7633458	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0008066	PMID:8586427;PMID:7633458	PCS		2/2			P	HPO:probinson[2022-05-11]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0000007	PMID:8586427	PCS					I	HPO:probinson[2022-05-11]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0001522	PMID:7633458	PCS		1/1			C	HPO:probinson[2022-05-11]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0200097	PMID:8586427;PMID:7633458	PCS		2/2			P	HPO:probinson[2022-05-11]
OMIM:619784	Epidermolysis bullosa, junctional 2B, severe		HP:0020117	PMID:7633458	PCS		1/1			P	HPO:probinson[2022-05-11]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0002169	OMIM:300750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0003487	OMIM:300750	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0002495	OMIM:300750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0010550	OMIM:300750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0001419	OMIM:300750	TAS					I	HPO:skoehler[2012-11-20]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0002064	OMIM:300750	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0001258	OMIM:300750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0003677	OMIM:300750	IEA					C	HPO:skoehler[2010-06-19]
OMIM:300750	Spastic paraplegia 34, X-linked		HP:0001347	OMIM:300750	IEA					P	HPO:skoehler[2010-06-19]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001773	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001377	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0004322	PMID:37352860	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000243	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001290	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0009380	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0009623	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001802	PMID:37352860	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001763	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001249	PMID:37352860	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000358	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002750	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0004570	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0003083	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0005180	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0040022	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0010760	PMID:37352860	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002827	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0040024	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000926	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000767	PMID:37352860	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000007	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0004209	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000768	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000400	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000520	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000369	PMID:37352860	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0008846	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000126	PMID:37352860	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001611	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0005019	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000220	PMID:37352860	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000341	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000582	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0003577	PMID:37352860	PCS		3/5			C	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001156	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0030674	PMID:37352860	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001270	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0010669	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0006094	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001629	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000938	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0009487	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0008551	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002999	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000218	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000076	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0009826	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0004279	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002650	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000750	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002099	PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0003184	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002092	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001159	PMID:37352860	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000268	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002645	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0002007	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0001631	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620663	Spondyloepimetaphyseal dysplasia, Guo-Campeau type		HP:0000347	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:109900	Blepharochalasis and double lip		HP:0010749	OMIM:109900	TAS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-06]
OMIM:109900	Blepharochalasis and double lip		HP:0040295	OMIM:109900	TAS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:109900	Blepharochalasis and double lip		HP:0000006	OMIM:109900	TAS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:109900	Blepharochalasis and double lip		HP:0000853	OMIM:109900	TAS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-06]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0003577	OMIM:610978	IEA					C	HPO:iea[2009-02-17]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0030830	PMID:28732825	PCS					P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0030874	PMID:28732825	PCS		5/6			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001332	OMIM:610978	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001252	PMID:9565498	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001251	PMID:9565498	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001290	OMIM:610978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001270	OMIM:610978	IEA					P	HPO:iea[2009-02-17]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0100750	PMID:28732825	PCS		2/13			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0032976	PMID:28732825	PCS		1/6			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0032977	PMID:28732825	PCS		3/6			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001629	PMID:24714694	PCS					P	HPO:probinson[2017-08-27]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0008213	PMID:30927038	PCS		1/2			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0000851	OMIM:610978	IEA					P	HPO:iea[2009-02-17]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0003623	PMID:9565498	PCS		1/1			C	HPO:probinson[2022-03-31]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002113	PMID:28732825	PCS		7/13			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002136	PMID:15289765	PCS		2/2			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001266	PMID:15289765	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0025394	PMID:28732825	PCS		1/13			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001288	OMIM:610978	TAS					P	HPO:probinson[2009-02-17]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002098	OMIM:610978	TAS	HP:0003623				P	HPO:skoehler[2013-06-06]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002099	OMIM:610978	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001260	PMID:15289765	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001263	PMID:9565498;PMID:15289765	PCS		3/3			P	HPO:probinson[2022-03-31];HPO:skoehler[2014-04-04];HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0025179	PMID:28732825	PCS		5/13			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0012735	PMID:28732825	PCS					P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0030828	PMID:28732825	PCS					P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0012418	PMID:28732825	PCS		6/7			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002091	PMID:28732825	PCS		2/5			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0032177	PMID:30927038	PCS		4/6			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0009797	PMID:28732825	PCS		2/16			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0008223	OMIM:610978	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002925	PMID:9565498;PMID:15289765	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31];HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0000824	PMID:30927038	PCS		1/2			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002205	PMID:9565498	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0001631	PMID:24714694	PCS					P	HPO:probinson[2017-08-27]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002206	PMID:28732825	PCS		1/16			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002789	PMID:28732825	PCS		10/16			P	HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0000006	PMID:15289765	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-05]
OMIM:610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress		HP:0002643	PMID:9565498;PMID:15289765	PCS	HP:0003623	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31];HPO:probinson[2021-05-05]
OMIM:161470	Nasal alar collapse, bilateral		HP:0000271	OMIM:161470	IEA					P	HPO:iea[2009-02-17]
OMIM:161470	Nasal alar collapse, bilateral		HP:0000006	OMIM:161470	IEA					I	HPO:iea[2009-02-17]
OMIM:604919	Becker nevus syndrome		HP:0000891	PMID:26564089	PCS					P	HPO:probinson[2020-04-27]
OMIM:604919	Becker nevus syndrome		HP:0003764	PMID:9024572	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-04-27]
OMIM:604919	Becker nevus syndrome		HP:0002650	PMID:26564089	PCS					P	HPO:probinson[2020-04-27]
OMIM:604919	Becker nevus syndrome		HP:0002937	PMID:26564089	PCS					P	HPO:probinson[2020-04-27]
OMIM:604919	Becker nevus syndrome		HP:0000767	PMID:26564089	IEA					P	HPO:probinson[2020-04-27]
OMIM:604919	Becker nevus syndrome		HP:0012813	PMID:9024572	PCS					P	HPO:probinson[2020-04-27]
OMIM:125540	Dermal ridges, patternless		HP:0000006	OMIM:125540	IEA					I	HPO:iea[2009-02-17]
OMIM:125540	Dermal ridges, patternless		HP:0000951	OMIM:125540	IEA					P	HPO:iea[2009-02-17]
OMIM:609583	Joubert syndrome 4		HP:0003774	PMID:15138899	PCS		1/2			P	HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0001320	PMID:15138899	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0000571	PMID:15138899	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0003577	PMID:15138899	PCS		1/1			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0000083	PMID:15138899	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0001252	PMID:15138899	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0001263	PMID:15138899	PCS		1/2			P	HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0001251	PMID:15138899	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0001290	OMIM:609583	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609583	Joubert syndrome 4		HP:0002172	PMID:15138899	PCS		1/2			P	HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0000090	OMIM:609583	IEA					P	HPO:iea[2009-02-17]
OMIM:609583	Joubert syndrome 4		HP:0002194	PMID:15138899	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0011933	OMIM:609583	TAS					P	HPO:probinson[2012-06-10]
OMIM:609583	Joubert syndrome 4		HP:0000639	PMID:15138899	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0100957	OMIM:609583	IEA					P	HPO:iea[2009-02-17]
OMIM:609583	Joubert syndrome 4		HP:0000657	OMIM:609583	IEA					P	HPO:iea[2009-02-17]
OMIM:609583	Joubert syndrome 4		HP:0002419	OMIM:609583	IEA					P	HPO:iea[2009-02-17]
OMIM:609583	Joubert syndrome 4		HP:0000007	PMID:15138899	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609583	Joubert syndrome 4		HP:0002404	PMID:15138899	PCS		1/2			P	HPO:probinson[2012-06-10];HPO:probinson[2022-09-02]
OMIM:617965	Spermatogenic failure 27		HP:0032560	PMID:29365104	PCS		2/2			P	HPO:probinson[2023-03-08]
OMIM:617965	Spermatogenic failure 27		HP:0003251	PMID:29365104	PCS		2/2			P	HPO:probinson[2023-03-08]
OMIM:617965	Spermatogenic failure 27		HP:0011462	PMID:29365104	PCS		2/2			C	HPO:probinson[2023-03-08]
OMIM:617965	Spermatogenic failure 27		HP:0000007	PMID:29365104	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-08]
OMIM:617965	Spermatogenic failure 27		HP:0012207	PMID:29365104	PCS		2/2			P	HPO:probinson[2023-03-08]
OMIM:617965	Spermatogenic failure 27		HP:0033525	PMID:29365104	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617965	Spermatogenic failure 27		HP:0032558	PMID:29365104	PCS		2/2			P	HPO:probinson[2023-03-08]
OMIM:617965	Spermatogenic failure 27		HP:0032559	PMID:29365104	PCS		2/2			P	HPO:probinson[2023-03-08]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0002465	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0002015	PMID:35148830	PCS		8/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0003236	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0000651	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0001260	PMID:35148830	PCS		9/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0002460	PMID:35148830	PCS		10/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0001284	PMID:35148830	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0002174	PMID:35148830	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0012548	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0030319	PMID:35148830	PCS		9/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0011462	PMID:35148830	PCS		2/2			C	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0000508	PMID:35148830	PCS		10/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0003805	PMID:35148830	PCS		10/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0003736	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0000218	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0000006	PMID:35148830	PCS					I	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0001337	PMID:35148830	PCS		1/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0000544	PMID:35148830	PCS		8/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0003458	PMID:35148830	PCS		10/10			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0001611	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:619790	Oculopharyngodistal myopathy 4		HP:0003557	PMID:35148830	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0003596	PMID:24627108	PCS		1/1			C	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0003431	PMID:32949214	PCS					P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0001288	PMID:32949214	PCS		4/4			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0001761	PMID:32949214	PCS		4/4			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0002460	PMID:32949214	PCS		4/5			P	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0003393	PMID:32949214	PCS		1/4			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0011463	PMID:32949214	PCS		1/3			C	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0011462	PMID:32949214	PCS		2/3			C	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0009830	PMID:24627108	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0002936	PMID:32949214	PCS		5/5			P	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0000006	PMID:24627108	PCS					I	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0002522	PMID:24627108	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620111	Charcot-Marie-Tooth disease, demyelinating, type 1J		HP:0001765	PMID:32949214	PCS		3/4			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0001298	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0000252	OMIM:615182	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0001321	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0010307	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0011968	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0001250	PMID:23561848	PCS		12/12			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-03-16]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:6000246	OMIM:615182	TAS					P	HPO:probinson[2024-05-09]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0001263	PMID:23561848	PCS		11/11			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-03-16]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0006829	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0001252	PMID:23561848	PCS		10/10			P	HPO:probinson[2023-03-16]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0002240	OMIM:615182	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0012448	OMIM:615182	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0002094	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0002093	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0012402	PMID:23561848	PCS		9/11			P	HPO:probinson[2023-03-16]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:6000509	OMIM:615182	TAS					P	HPO:probinson[2024-05-09]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0100704	OMIM:615182	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0000737	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0000817	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0040144	PMID:23561848	PCS		12/12			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-16]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0000007	PMID:23561848	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2023-03-16]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0002119	OMIM:615182	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0000256	OMIM:615182	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:615182	Combined D-2- and L-2-hydroxyglutaric aciduria		HP:0033092	PMID:23561848	PCS		7/8			P	HPO:probinson[2023-03-16]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001265	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0000970	PMID:16534117	TAS					P	HPO:probinson[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001069	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0002661	OMIM:201300	TAS					P	HPO:probinson[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001252	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001284	PMID:16534117	PCS					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0002020	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0003593	OMIM:201300	IEA					C	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001290	OMIM:201300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0003380	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0009771	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0007460	OMIM:201300	TAS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0008000	OMIM:201300	TAS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001939	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001818	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0006121	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0009830	OMIM:201300	IEA					P	HPO:skoehler[2015-01-27]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0000007	OMIM:201300	IEA					I	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0008872	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0003448	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0000224	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0000762	OMIM:201300	TAS					P	HPO:probinson[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0003677	OMIM:201300	PCS					C	HPO:iea[2009-02-17]
OMIM:201300	Neuropathy, hereditary sensory and autonomic, type II		HP:0001842	OMIM:201300	IEA					P	HPO:iea[2009-02-17]
OMIM:606840	Faciomandibular myoclonus, nocturnal		HP:0003763	OMIM:606840	TAS					P	HPO:probinson[2013-04-01]
OMIM:606840	Faciomandibular myoclonus, nocturnal		HP:0001336	OMIM:606840	TAS					P	HPO:skoehler[2009-02-17]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0001254	PMID:35321494	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0003236	PMID:35321494	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0002015	PMID:35321494	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0003577	PMID:35321494	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0000590	PMID:35321494	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0011924	PMID:35321494	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0001252	PMID:35321494	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0001263	PMID:35321494	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0001284	PMID:35321494	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0002194	PMID:35321494	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0011923	PMID:35321494	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0002919	PMID:35321494	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0001508	PMID:35321494	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0000508	PMID:35321494	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0012120	PMID:35321494	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0000007	PMID:35321494	PCS					I	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0002878	PMID:35321494	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0008347	PMID:35321494	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0003648	PMID:35321494	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0003803	PMID:35321494	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0003701	PMID:35321494	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:620139	Combined oxidative phosphorylation deficiency 56		HP:0003557	PMID:35321494	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-12]
OMIM:248700	Marden-Walker syndrome		HP:0000286	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000486	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001651	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000089	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0002021	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001250	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0003199	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000160	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001252	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001290	OMIM:248700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:248700	Marden-Walker syndrome		HP:0000316	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0008897	OMIM:248700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248700	Marden-Walker syndrome		HP:0005329	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001249	PMID:24726473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:248700	Marden-Walker syndrome		HP:0002974	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0002476	OMIM:248700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:248700	Marden-Walker syndrome		HP:0000175	PMID:24726473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:248700	Marden-Walker syndrome		HP:0000252	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000054	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0012385	OMIM:248700	TAS					P	HPO:skoehler[2013-10-22]
OMIM:248700	Marden-Walker syndrome		HP:0000766	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0002705	OMIM:248700	TAS					P	HPO:skoehler[2015-12-30]
OMIM:248700	Marden-Walker syndrome		HP:0000568	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000047	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000006	PMID:24726473	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-14]
OMIM:248700	Marden-Walker syndrome		HP:0000369	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0003577	PMID:24726473	PCS		1/1			C	HPO:probinson[2022-12-14]
OMIM:248700	Marden-Walker syndrome		HP:0000343	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0002089	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000463	OMIM:248700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:248700	Marden-Walker syndrome		HP:0002365	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000023	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000260	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0002044	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001274	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000581	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0007068	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001305	PMID:24726473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:248700	Marden-Walker syndrome		HP:0000218	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001166	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0002650	PMID:24726473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:248700	Marden-Walker syndrome		HP:0001762	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001321	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000470	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0009473	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0002808	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000508	PMID:24726473	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-12-14]
OMIM:248700	Marden-Walker syndrome		HP:0002803	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0001511	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000028	OMIM:248700	IEA					P	HPO:iea[2009-02-17]
OMIM:248700	Marden-Walker syndrome		HP:0000347	PMID:24726473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:602398	Desmosterolosis		HP:0034937	PMID:29175559	PCS		10/10			P	HPO:probinson[2023-07-18];HPO:probinson[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0000286	PMID:29175559	PCS		1/10			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000486	PMID:29175559	PCS		6/9			P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0004322	PMID:29175559	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0001250	PMID:29175559	PCS		5/8			P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0003196	OMIM:602398	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0004482	PMID:29175559	PCS		2/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0000639	PMID:29175559	PCS		6/9			P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0000238	OMIM:602398	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0003107	PMID:11519011	PCS		2/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001643	PMID:12457401	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000358	PMID:9450875	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000175	PMID:29175559	PCS		4/10			P	HPO:iea[2012-04-24];HPO:probinson[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0000494	PMID:29175559	PCS		4/10			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000252	PMID:29175559	PCS		5/10			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001263	PMID:29175559	PCS		9/9			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000007	PMID:11519011	PCS					I	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001338	OMIM:602398	TAS					P	HPO:skoehler[2013-06-05]
OMIM:602398	Desmosterolosis		HP:0000169	PMID:9450875	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001257	PMID:29175559	PCS		7/7			P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0000369	PMID:29175559	PCS		4/10			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001776	PMID:12457401	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000341	PMID:29175559	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0008905	PMID:29175559	PCS		2/5			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000463	OMIM:602398	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0000061	PMID:9450875	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001274	PMID:29175559	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0009085	PMID:9450875	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001508	PMID:29175559	PCS		8/9			P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0011001	PMID:29175559	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0002119	PMID:29175559	PCS		9/10			P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0000378	PMID:12457401	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000256	PMID:29175559	PCS		1/10			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000773	PMID:29175559	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0005789	PMID:9450875	PCS	HP:0003577	1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000033	PMID:12457401	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0001883	PMID:29175559	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0005684	PMID:29175559	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0000470	PMID:29175559	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0005281	PMID:9450875	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0005160	PMID:29175559	PCS		1/6			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0007370	PMID:29175559	PCS		2/2			P	HPO:iea[2012-04-24];HPO:probinson[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0034295	PMID:29175559	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0009473	PMID:12457401	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000506	PMID:29175559	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0002804	OMIM:602398	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602398	Desmosterolosis		HP:0000268	PMID:29175559	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:602398	Desmosterolosis		HP:0002007	PMID:29175559	PCS		1/9			P	HPO:iea[2012-04-24]
OMIM:602398	Desmosterolosis		HP:0000347	PMID:29175559	PCS		9/10			P	HPO:iea[2012-04-24]
OMIM:604931	Cortisone reductase deficiency 1		HP:0003621	PMID:18628520	PCS		1/4			C	HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0003596	PMID:18628520	PCS		1/4			C	HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0001596	PMID:18628520	PCS		1/4			P	HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0000826	PMID:18628520	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0003581	PMID:18628520	PCS		1/4			C	HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0000789	PMID:18628520	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0000876	PMID:18628520	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0000007	PMID:18628520	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0001061	PMID:18628520	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0025710	PMID:18628520	PCS		1/4			C	HPO:probinson[2022-09-11]
OMIM:604931	Cortisone reductase deficiency 1		HP:0001513	OMIM:604931	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604931	Cortisone reductase deficiency 1		HP:0001007	PMID:18628520	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:276822	Ulnar agenesis and endocardial fibroelastosis		HP:0003982	OMIM:276822	TAS					P	HPO:probinson[2012-07-17]
OMIM:276822	Ulnar agenesis and endocardial fibroelastosis		HP:0001706	OMIM:276822	IEA					P	HPO:iea[2009-02-17]
OMIM:276822	Ulnar agenesis and endocardial fibroelastosis		HP:0001789	OMIM:276822	IEA					P	HPO:iea[2009-02-17]
OMIM:276822	Ulnar agenesis and endocardial fibroelastosis		HP:0000007	OMIM:276822	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:276822	Ulnar agenesis and endocardial fibroelastosis		HP:0003811	OMIM:276822	IEA					C	HPO:iea[2009-02-17]
OMIM:276822	Ulnar agenesis and endocardial fibroelastosis		HP:0009380	OMIM:276822	IEA					P	HPO:iea[2009-02-17]
OMIM:113970	Burkitt lymphoma		HP:0001442	OMIM:113970	IEA					I	HPO:skoehler[2019-04-18]
OMIM:113970	Burkitt lymphoma		HP:0003745	OMIM:113970	TAS					I	HPO:skoehler[2015-12-30]
OMIM:113970	Burkitt lymphoma		HP:0030080	OMIM:113970	TAS					P	HPO:skoehler[2015-01-21]
OMIM:113970	Burkitt lymphoma		HP:0002721	OMIM:113970	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000286	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000582	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0010804	PMID:24726472	PCS		3/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0001212	PMID:24726472	PCS		2/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0001252	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0003593	PMID:24726472	PCS		4/4			C	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0001270	PMID:24726472	PCS		4/4		HP:0012825	P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0012368	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0002719	PMID:24726472	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0007021	PMID:24726472	PCS		3/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000817	PMID:24726472	PCS		3/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000718	PMID:24726472	PCS		3/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000717	PMID:24726472	PCS		3/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0005709	PMID:24726472	PCS		2/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000712	PMID:24726472	PCS		3/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000218	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000179	PMID:24726472	PCS		3/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0001249	PMID:24726472	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0002213	PMID:24726472	PCS		3/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0001288	PMID:24726472	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0002376	PMID:24726472	PCS		2/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0001382	PMID:24726472	PCS		2/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0001263	PMID:24726472	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0011228	PMID:24726472	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000349	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0002007	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000960	PMID:24726472	PCS		2/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000303	PMID:24726472	PCS		3/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000248	PMID:24726472	PCS		1/4			P	HPO:probinson[2023-01-26]
OMIM:615828	Vulto-van Silfout-de Vries syndrome		HP:0000006	PMID:24726472	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-26]
OMIM:136500	Focal facial dermal dysplasia 1, Brauer type		HP:0011336	PMID:19291768	PCS					P	HPO:probinson[2020-08-02]
OMIM:136500	Focal facial dermal dysplasia 1, Brauer type		HP:0009743	PMID:19291768	PCS					P	HPO:probinson[2020-08-02]
OMIM:136500	Focal facial dermal dysplasia 1, Brauer type		HP:0000006	PMID:19291768	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-08-02]
OMIM:136500	Focal facial dermal dysplasia 1, Brauer type		HP:0000369	PMID:19291768	PCS					P	HPO:probinson[2020-08-02]
OMIM:136500	Focal facial dermal dysplasia 1, Brauer type		HP:0005338	PMID:19291768	PCS					P	HPO:probinson[2020-08-02]
OMIM:617959	Spermatogenic failure 24		HP:0032560	PMID:29606301	PCS					P	HPO:probinson[2019-09-07]
OMIM:617959	Spermatogenic failure 24		HP:0032561	PMID:29606301	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-07]
OMIM:617959	Spermatogenic failure 24		HP:0032562	PMID:29606301	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-07]
OMIM:617959	Spermatogenic failure 24		HP:0000007	PMID:29606301	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:617959	Spermatogenic failure 24		HP:0012207	PMID:29606301	TAS		2/2			P	HPO:probinson[2019-06-13];HPO:probinson[2019-06-13]
OMIM:617959	Spermatogenic failure 24		HP:0032559	PMID:29606301	PCS					P	HPO:probinson[2019-09-07]
OMIM:617781	Retinitis pigmentosa 80		HP:0007737	PMID:26216056	PCS		1/1			P	HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0003621	PMID:26968735	PCS		3/8			C	HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0000662	PMID:26216056	PCS	HP:0011463	1/1			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0000529	PMID:26216056	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0011463	PMID:26216056;PMID:26968735	PCS		2/9			C	HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0001263	OMIM:617781	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617781	Retinitis pigmentosa 80		HP:0010230	OMIM:617781	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617781	Retinitis pigmentosa 80		HP:0011462	PMID:26968735	PCS		4/8			C	HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0000618	OMIM:617781	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617781	Retinitis pigmentosa 80		HP:0000007	PMID:26216056	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0007401	PMID:26968735	PCS		3/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617781	Retinitis pigmentosa 80		HP:0007843	PMID:26968735	PCS		3/8			P	HPO:probinson[2022-10-30]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001276	PMID:11845408	PCS		3/3			P	HPO:iea[2009-02-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0002136	OMIM:606854	IEA					P	HPO:iea[2009-02-17]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0003577	PMID:11845408	IEA		5/5			C	HPO:probinson[2021-05-02]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0002078	PMID:11845408	PCS		3/3			P	HPO:iea[2009-02-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0003487	OMIM:606854	IEA					P	HPO:iea[2009-02-17]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001321	OMIM:606854	IEA					P	HPO:iea[2009-02-17]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001310	PMID:11845408	PCS		3/3			P	HPO:skoehler[2018-10-08];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0002365	OMIM:606854	IEA					P	HPO:iea[2009-02-17]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001250	PMID:11845408	PCS		4/5			P	HPO:iea[2009-02-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001263	PMID:11845408	PCS		5/5			P	HPO:probinson[2012-04-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0011448	PMID:11845408	PCS		1/5			P	HPO:probinson[2012-04-17];HPO:probinson[2021-05-02]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0012110	PMID:11845408	PCS		2/2		HP:0012825	P	HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0012650	PMID:11845408	PCS		5/5			P	HPO:probinson[2021-05-02]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0000639	OMIM:606854	IEA					P	HPO:iea[2009-02-17]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0007266	OMIM:606854	TAS					P	HPO:probinson[2012-04-17]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001999	PMID:11845408	PCS		0/5			P	HP:probinson[2019-03-10];HPO:probinson[2024-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0000007	PMID:11845408	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0002119	PMID:11845408	PCS		2/2			P	HP:probinson[2019-03-10];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0000565	PMID:11845408	PCS		5/5			P	HPO:iea[2009-02-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001249	PMID:11845408	PCS		5/5			P	HPO:probinson[2012-04-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0006821	PMID:11845408	PCS		2/2			P	HPO:iea[2009-02-17];HP:probinson[2019-03-10]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0000577	OMIM:606854	IEA					P	HPO:iea[2009-02-17]
OMIM:606854	Polymicrogyria, bilateral frontoparietal		HP:0001347	PMID:11845408	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0033803	PMID:8618021	PCS					P	HPO:probinson[2022-08-15]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0003577	PMID:8618021	PCS					C	HPO:probinson[2022-08-15]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0001030	PMID:8618021	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-15]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0007383	PMID:8618021	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-15]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0008066	PMID:8618021	PCS					P	HPO:probinson[2022-08-15]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0008404	PMID:8618021	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2022-08-15]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0000006	PMID:8618021	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-15]
OMIM:132000	Epidermolysis bullosa with congenital localized absence of skin anddeformity of nails		HP:0200097	PMID:8618021	PCS					P	HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0011939	PMID:17546030	PCS		1/1			P	HPO:probinson[2024-07-22]
OMIM:305600	Focal dermal hypoplasia		HP:0001374	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001770	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000684	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000486	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0004322	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001010	PMID:17546030	PCS		1/1		HP:0025293	P	HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0000085	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0010049	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001171	PMID:17546030	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0003191	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0009380	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0009381	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001849	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000639	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001807	PMID:17546030	PCS		1/1			P	HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0001009	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000238	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001802	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001249	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000677	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001540	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002036	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000175	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000252	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0004334	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002232	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002475	OMIM:305600	TAS					P	HPO:skoehler[2014-04-04]
OMIM:305600	Focal dermal hypoplasia		HP:0001382	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000528	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0010044	PMID:17546030	PCS		1/1			P	HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0001817	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002308	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001537	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000689	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000568	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0007510	PMID:17546030	PCS		1/1			P	HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0001539	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000648	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000526	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0008404	OMIM:305600	TAS					P	HPO:skoehler[2015-12-30]
OMIM:305600	Focal dermal hypoplasia		HP:0000567	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000204	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000369	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000446	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000402	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000324	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000126	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000066	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0003577	PMID:17546030	PCS		1/1			C	HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0030037	OMIM:305600	TAS					P	HPO:skoehler[2014-09-21]
OMIM:305600	Focal dermal hypoplasia		HP:0001156	OMIM:305600	TAS					P	HPO:skoehler[2014-11-26]
OMIM:305600	Focal dermal hypoplasia		HP:0000023	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002164	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0006608	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0003298	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001274	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000060	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0010740	OMIM:305600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:305600	Focal dermal hypoplasia		HP:0008070	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0010743	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001829	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0006297	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000612	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0007663	OMIM:305600	TAS					P	HPO:skoehler[2015-07-26]
OMIM:305600	Focal dermal hypoplasia		HP:0007588	OMIM:305600	TAS					P	HPO:iea[2012-06-10]
OMIM:305600	Focal dermal hypoplasia		HP:0000455	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002557	OMIM:305600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001423	PMID:17546030	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0007546	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000410	OMIM:305600	TAS					P	HPO:probinson[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000773	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002558	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000776	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0009803	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001545	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0006638	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002650	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002299	OMIM:305600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001162	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000073	OMIM:305600	TAS					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0001083	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0033001	OMIM:305600	TAS					P	HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0001839	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000668	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000307	PMID:17546030	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-15]
OMIM:305600	Focal dermal hypoplasia		HP:0000505	OMIM:305600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:305600	Focal dermal hypoplasia		HP:0000028	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:305600	Focal dermal hypoplasia		HP:0002566	OMIM:305600	IEA					P	HPO:iea[2009-02-17]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0002465	OMIM:615419	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0003676	OMIM:615419	TAS					C	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0003577	PMID:23749988	PCS		2/2			C	HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0003431	OMIM:615419	TAS					P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000486	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0001250	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0003196	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0002020	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000639	OMIM:615419	TAS					P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000319	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000817	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0011220	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0008897	OMIM:615419	TAS				HP:0012828	P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000417	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000219	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0002019	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0001347	OMIM:615419	TAS					P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0008936	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0003202	OMIM:615419	TAS					P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000154	OMIM:615419	TAS					P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000252	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0002510	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0002650	PMID:23749988	PCS		1/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0001344	PMID:23749988	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0002376	PMID:23749988	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0011968	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0001263	PMID:23749988;OMIM:615419	PCS		12/12		HP:0012829	P	HPO:skoehler[2019-02-22];HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0034392	PMID:23749988	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0007256	OMIM:615419	TAS					P	HPO:skoehler[2015-01-04]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000007	PMID:23749988	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000648	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000768	PMID:23749988	PCS		1/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000400	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0001511	PMID:23749988	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000248	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000028	PMID:23749988	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000369	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000347	PMID:23749988	PCS		2/2			P	HPO:skoehler[2013-09-30]
OMIM:615419	Hypotonia, infantile, with psychomotor retardation and characteristic facies 1		HP:0000325	OMIM:615419	TAS					P	HPO:skoehler[2013-11-18]
OMIM:612376	Acute promyelocytic leukemia		HP:0012135	OMIM:612376	TAS					P	HPO:skoehler[2013-01-09]
OMIM:612376	Acute promyelocytic leukemia		HP:0001442	PMID:1652368	PCS					I	HPO:probinson[2013-12-15]
OMIM:612376	Acute promyelocytic leukemia		HP:0004836	OMIM:612376	TAS					P	HPO:skoehler[2013-01-10]
OMIM:613068	Neurodegeneration due to cerebral folate transport deficiency		HP:0002376	OMIM:613068	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613068	Neurodegeneration due to cerebral folate transport deficiency		HP:0001250	OMIM:613068	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613068	Neurodegeneration due to cerebral folate transport deficiency		HP:0000007	OMIM:613068	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613068	Neurodegeneration due to cerebral folate transport deficiency		HP:0002180	OMIM:613068	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613068	Neurodegeneration due to cerebral folate transport deficiency		HP:0001249	OMIM:613068	IEA					P	HPO:skoehler[2010-06-20]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0002014	OMIM:266600	TAS					P	HPO:iea[2009-02-17]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0002037	OMIM:266600	TAS					P	HPO:skoehler[2015-01-21]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0005214	OMIM:266600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0100279	OMIM:266600	TAS					P	HPO:skoehler[2015-01-21]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0100280	OMIM:266600	TAS					P	HPO:probinson[2020-07-07]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0032154	OMIM:266600	TAS					P	HPO:probinson[2020-07-07]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0010982	OMIM:266600	TAS					I	HPO:probinson[2025-06-05]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0001824	OMIM:266600	TAS					P	HPO:iea[2009-02-17]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0001510	OMIM:266600	TAS					P	HPO:skoehler[2015-01-21]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0002027	OMIM:266600	TAS					P	HPO:iea[2009-02-17]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0011107	OMIM:266600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:266600	Inflammatory bowel disease 1, Crohn disease		HP:0100819	OMIM:266600	TAS					P	HPO:probinson[2025-06-05]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0010628	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0003676	OMIM:614707	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0006824	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001992	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001252	OMIM:614707	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001251	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001290	OMIM:614707	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0003690	OMIM:614707	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001171	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0000639	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0007141	OMIM:614707	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0003828	OMIM:614707	TAS					M	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0000718	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001308	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0003700	OMIM:614707	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0002751	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0000572	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0002015	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0002312	OMIM:614707	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0002375	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0002650	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001283	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0001284	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0002093	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0000407	OMIM:614707	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0000007	OMIM:614707	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0000648	OMIM:614707	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614707	Brown-Vialetto-Van laere syndrome 2		HP:0000467	OMIM:614707	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619223	Immunodeficiency 77		HP:0008619	PMID:33224153	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0031292	PMID:33224153	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0032261	PMID:28422754	PCS		4/4			P	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0002110	PMID:28422754	PCS		4/4			P	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0003581	PMID:28422754	PCS		4/4			C	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0011110	PMID:33224153	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0100658	PMID:33224153	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0006510	PMID:28422754	PCS		1/4			P	HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0000006	PMID:28422754	PCS					I	HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:619223	Immunodeficiency 77		HP:0002578	PMID:33224153	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:619545	Hypoplastic femurs and pelvis		HP:0008839	PMID:34433009	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619545	Hypoplastic femurs and pelvis		HP:0003097	PMID:34433009	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619545	Hypoplastic femurs and pelvis		HP:0000006	PMID:34433009	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:618883	Hypoparathyroidism, familial isolated 2		HP:0002199	PMID:11602629;PMID:15863676	PCS		3/4			P	HPO:probinson[2021-07-04]
OMIM:618883	Hypoparathyroidism, familial isolated 2		HP:0031817	PMID:11602629;PMID:15863676	PCS		4/4			P	HPO:probinson[2021-07-04]
OMIM:618883	Hypoparathyroidism, familial isolated 2		HP:0002905	PMID:15863676	PCS		1/2			P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:618883	Hypoparathyroidism, familial isolated 2		HP:0000007	PMID:11602629	PCS					I	HPO:probinson[2021-07-04]
OMIM:618883	Hypoparathyroidism, familial isolated 2		HP:0002901	PMID:15863676	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:262300	Achromatopsia 3		HP:0007803	OMIM:262300	TAS					P	HPO:probinson[2009-02-17]
OMIM:262300	Achromatopsia 3		HP:0000639	PMID:10888875	PCS		3/3			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:262300	Achromatopsia 3		HP:0000518	OMIM:262300	TAS					P	HPO:probinson[2009-02-17]
OMIM:262300	Achromatopsia 3		HP:0001141	OMIM:262300	TAS					P	HPO:probinson[2012-08-01]
OMIM:262300	Achromatopsia 3		HP:0000613	PMID:10888875	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-19]
OMIM:262300	Achromatopsia 3		HP:0007641	PMID:10888875	PCS		1/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-19]
OMIM:262300	Achromatopsia 3		HP:0000007	PMID:10888875	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-19]
OMIM:262300	Achromatopsia 3		HP:0011003	OMIM:262300	TAS					P	HPO:probinson[2012-04-01]
OMIM:262300	Achromatopsia 3		HP:0011516	PMID:10888875	PCS		2/3			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-02-19]
OMIM:262300	Achromatopsia 3		HP:0007811	OMIM:262300	TAS					P	HPO:probinson[2012-04-01]
OMIM:262300	Achromatopsia 3		HP:0030515	PMID:10888875	PCS		3/3			P	HPO:probinson[2023-02-19]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0003577	PMID:19843503	PCS		2/4			C	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0002023	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000365	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000486	PMID:19843503	PCS		1/4			P	HPO:skoehler[2018-10-08]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0001195	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0012805	PMID:19843503	PCS		3/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0001010	PMID:33878481	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000020	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0003593	PMID:19843503	PCS		1/4			C	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0003010	PMID:19843503	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0031364	PMID:33878481	PCS		2/2			P	HPO:probinson[2022-04-05]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000639	PMID:19843503;PMID:33878481	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-05];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000613	PMID:33878481	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-05]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0001107	PMID:19843503	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0007443	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0007663	PMID:19843503	PCS		4/4			P	HPO:skoehler[2018-10-08]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000978	PMID:19843503;PMID:33878481	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-05];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0001104	OMIM:614075	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000011	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0001022	PMID:19843503	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0030127	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000010	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0001583	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0004871	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0001263	PMID:19843503	PCS		1/4			P	HPO:skoehler[2019-04-18]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0030825	PMID:19843503	PCS		1/4			P	HPO:skoehler[2018-10-08]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0011870	PMID:19843503	PCS		1/1			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0033263	PMID:19843503	PCS		3/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0002607	PMID:19843503	PCS		1/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0008320	PMID:19843503	PCS		1/1			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000646	PMID:33878481	PCS		2/2			P	HPO:probinson[2022-04-05]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000007	OMIM:614075	IEA					I	HPO:probinson[2013-08-10]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0002788	PMID:19843503	PCS		1/4			P	HPO:skoehler[2018-10-08]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000421	PMID:19843503	PCS		2/4			P	HPO:probinson[2013-08-10]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0002206	PMID:19843503	PCS		0/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0000666	PMID:19843503	PCS		2/4			P	HPO:probinson[2024-03-15]
OMIM:614075	Hermansky-Pudlak syndrome 6		HP:0004866	PMID:19843503	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:151000	Lentiginosis, centrofacial neurodysraphic		HP:0000006	OMIM:151000	IEA					I	HPO:iea[2009-02-17]
OMIM:151000	Lentiginosis, centrofacial neurodysraphic		HP:0001249	OMIM:151000	IEA					P	HPO:iea[2009-02-17]
OMIM:151000	Lentiginosis, centrofacial neurodysraphic		HP:0000951	OMIM:151000	IEA					P	HPO:iea[2009-02-17]
OMIM:222730	Dicarboxylicamino aciduria		HP:0003355	OMIM:222730	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222730	Dicarboxylicamino aciduria		HP:0000007	PMID:21123949	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-19]
OMIM:222730	Dicarboxylicamino aciduria		HP:0003162	OMIM:222730	IEA					P	HPO:iea[2009-02-17]
OMIM:222730	Dicarboxylicamino aciduria		HP:0032401	PMID:21123949	PCS		2/2			P	HP:probinson[2019-04-19];HP:probinson[2019-04-19]
OMIM:222730	Dicarboxylicamino aciduria		HP:0001249	OMIM:222730	IEA					P	HPO:iea[2009-02-17]
OMIM:222730	Dicarboxylicamino aciduria		HP:0000787	PMID:21123949	PCS	HP:0011462	1/2			P	HP:probinson[2019-04-19];HP:probinson[2019-04-19]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003555	OMIM:618129	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003236	PMID:27259757	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003621	PMID:27259757	PCS		1/29			C	HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003687	PMID:27259757	PCS					P	HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003596	PMID:27259757	PCS		8/29			C	HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0001288	OMIM:618129	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003198	PMID:27259757	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003584	PMID:27259757	PCS		1/29			C	HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003691	OMIM:618129	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0012548	PMID:27259757	PCS					P	HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0009023	OMIM:618129	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0011463	PMID:27259757	PCS		1/29			C	HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0011462	PMID:27259757	PCS		19/29			C	HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003307	OMIM:618129	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0007126	OMIM:618129	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003418	PMID:27259757	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003701	PMID:27259757	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0000006	OMIM:618129	IEA					I	HPO:skoehler[2019-04-18]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003326	PMID:27259757	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-13]
OMIM:618129	Muscular dystrophy, limb-girdle, autosomal dominant 4		HP:0003557	PMID:27259757	PCS					P	HPO:probinson[2022-12-13]
OMIM:118400	Cherubism		HP:0001133	PMID:12695257	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:0003621	PMID:16053841	PCS		17/24			C	HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0000189	PMID:16053841	PCS					P	HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:0030793	PMID:16053841	PCS		20/24			P	HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0001571	PMID:11113824	PCS					P	HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:6000715	PMID:29988246	PCS		1/1			P	HPO:probinson[2024-05-09]
OMIM:118400	Cherubism		HP:0030802	PMID:16053841	PCS		3/24			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0009085	PMID:16053841	PCS					P	HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0033176	PMID:16053841	PCS		10/24			P	HPO:probinson[2020-10-12]
OMIM:118400	Cherubism		HP:0011463	PMID:16053841	PCS		4/24			C	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0011462	PMID:16053841	PCS		3/24			C	HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0007663	PMID:12695257	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:0000689	PMID:16053841	PCS					P	HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:0000505	PMID:12695257	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:0200057	PMID:12695257	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:0200056	PMID:12695257	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2020-09-25]
OMIM:118400	Cherubism		HP:0000311	PMID:16053841	PCS		19/24			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0000520	OMIM:118400	IEA					P	HPO:iea[2009-02-17]
OMIM:118400	Cherubism		HP:0000006	PMID:16053841	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-23]
OMIM:118400	Cherubism		HP:0000677	OMIM:118400	IEA					P	HPO:iea[2009-02-17]
OMIM:118400	Cherubism		HP:0001138	PMID:12695257	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-25]
OMIM:155500	Macrodactyly, somatic		HP:0003577	PMID:23100325	PCS		6/6			C	HPO:probinson[2023-02-22]
OMIM:155500	Macrodactyly, somatic		HP:0001442	PMID:23100325	PCS		6/6			I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:155500	Macrodactyly, somatic		HP:0004099	PMID:23100325	PCS		6/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-22]
OMIM:127800	Dysplasia epiphysealis hemimelica		HP:0000924	OMIM:127800	IEA					P	HPO:iea[2009-02-17]
OMIM:127800	Dysplasia epiphysealis hemimelica		HP:0001548	OMIM:127800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:617232	Muscular dystrophy, limb-girdle, autosomal recessive 21		HP:0003202	PMID:27807076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0003236	PMID:27807076	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0003691	PMID:27807076	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0012548	PMID:27807076	PCS		4/4			P	HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0002093	OMIM:617232	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0002091	PMID:27807076	PCS		2/4			P	HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, autosomal recessive 21		HP:0030877	PMID:27807076	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0032341	PMID:27807076	PCS		2/4			P	HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0011462	PMID:27807076	PCS		4/4			C	HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0000007	PMID:27807076	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0006785	PMID:27807076	PCS		4/4			P	HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, autosomal recessive 21		HP:0002505	PMID:27807076	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0003677	PMID:27807076	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:617232	Muscular dystrophy, limb-girdle, type 2Z		HP:0006536	PMID:27807076	PCS		1/4			P	HPO:probinson[2023-02-12]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0005964	PMID:1677640	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001265	PMID:1677640	PCS		2/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0003577	PMID:1677640	PCS		6/6			C	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001278	PMID:1677640	PCS		6/6		HP:0012828	P	HPO:probinson[2013-08-09];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001156	PMID:1677640	PCS		2/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001250	PMID:1677640	PCS		2/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001382	PMID:1677640	PCS		3/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:6000234	PMID:11857564	PCS		2/2			P	HPO:probinson[2024-02-27]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:6000994	PMID:20301647	PCS					P	HPO:probinson[2024-08-04]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001252	PMID:1677640	PCS		2/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0005110	PMID:1677640	PCS		1/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0012877	PMID:1677640	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:6000556	PMID:11857564	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0030319	PMID:1677640	PCS		2/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0002917	PMID:1677640	PCS		2/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0000508	PMID:1677640	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0008202	PMID:1677640	PCS		4/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0000007	PMID:1677640	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001998	PMID:1677640	PCS		1/6			P	HPO:probinson[2013-08-09];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0000218	PMID:1677640	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0001742	PMID:1677640	PCS		3/6			P	HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0000017	PMID:1677640	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:223360	Orthostatic hypotension 1, due to DBH deficiency		HP:0003138	PMID:1677640	PCS		2/6			P	HPO:probinson[2022-05-31]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0008066	PMID:20164846	PCS	HP:0003593	1/1		HP:0031135	P	HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0008066	PMID:22113475	PCS		4/4			P	HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0001075	PMID:20164846	PCS		0/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0003593	PMID:22113475	PCS		1/1			C	HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0000007	PMID:20164846	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0008404	PMID:22113475	PCS		0/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0000972	PMID:22113475	PCS		0/1			P	HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0001810	PMID:20164846	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:615425	Epidermolysis bullosa simplex, autosomal recessive 2		HP:0032449	PMID:20164846;PMID:22113475	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0003621	PMID:22474227	PCS		1/7			C	HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0003596	PMID:22474227	PCS		1/7			C	HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0011463	PMID:22474227	PCS		3/7			C	HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0003584	PMID:22474227	PCS		1/7			C	HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0011462	PMID:22474227	PCS		1/7			C	HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0004890	PMID:22474227	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0003829	PMID:22474227	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0002094	OMIM:615343	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0002092	PMID:22474227	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0005317	PMID:22474227	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-18]
OMIM:615343	Pulmonary hypertension, primary, 3		HP:0000006	PMID:22474227	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-18]
OMIM:608474	Myopia 5		HP:0003577	PMID:12714612	PCS					C	HPO:probinson[2022-09-02]
OMIM:608474	Myopia 5		HP:0003621	PMID:12714612	PCS					C	HPO:probinson[2022-09-02]
OMIM:608474	Myopia 5		HP:0000541	OMIM:608474	IEA					P	HPO:iea[2009-02-17]
OMIM:608474	Myopia 5		HP:0011463	PMID:12714612	PCS					C	HPO:probinson[2022-09-02]
OMIM:608474	Myopia 5		HP:0011003	PMID:12714612	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608474	Myopia 5		HP:0000006	PMID:12714612	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:616892	Nephrotic syndrome, type 12		HP:0003774	OMIM:616892	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616892	Nephrotic syndrome, type 12		HP:0003676	OMIM:616892	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616892	Nephrotic syndrome, type 12		HP:0000097	OMIM:616892	PCS		5/5			P	HPO:probinson[2017-06-23]
OMIM:616892	Nephrotic syndrome, type 12		HP:0000790	OMIM:616892	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616892	Nephrotic syndrome, type 12		HP:0000007	PMID:26878725	PCS					I	HPO:probinson[2017-06-23]
OMIM:616892	Nephrotic syndrome, type 12		HP:0001967	OMIM:616892	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616892	Nephrotic syndrome, type 12		HP:0012588	OMIM:616892	PCS	HP:0011463	7/7			P	HPO:probinson[2017-06-23]
OMIM:618667	Hydrocephalus, congenital communicating, 1		HP:0001250	PMID:29983323	PCS		3/3			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618667	Hydrocephalus, congenital communicating, 1		HP:0012758	PMID:29983323	PCS		3/3			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618667	Hydrocephalus, congenital communicating, 1		HP:0002119	PMID:29983323	PCS		3/3			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618667	Hydrocephalus, congenital communicating, 1		HP:0001334	PMID:29983323	PCS	HP:0030674	3/3			P	HPO:probinson[2020-06-27]
OMIM:618667	Hydrocephalus, congenital communicating, 1		HP:0000006	PMID:29983323	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:601322	Porencephaly, cerebellar hypoplasia, and internal malformations		HP:0001696	OMIM:601322	IEA					P	HPO:iea[2009-02-17]
OMIM:601322	Porencephaly, cerebellar hypoplasia, and internal malformations		HP:0001321	OMIM:601322	IEA					P	HPO:iea[2009-02-17]
OMIM:601322	Porencephaly, cerebellar hypoplasia, and internal malformations		HP:0002132	OMIM:601322	TAS					P	HPO:probinson[2009-02-17]
OMIM:601322	Porencephaly, cerebellar hypoplasia, and internal malformations		HP:0001636	OMIM:601322	IEA					P	HPO:iea[2009-02-17]
OMIM:601322	Porencephaly, cerebellar hypoplasia, and internal malformations		HP:0000007	OMIM:601322	IEA					I	HPO:iea[2009-02-17]
OMIM:601322	Porencephaly, cerebellar hypoplasia, and internal malformations		HP:0001631	OMIM:601322	IEA					P	HPO:iea[2009-02-17]
OMIM:601322	Porencephaly, cerebellar hypoplasia, and internal malformations		HP:0002335	OMIM:601322	TAS					P	HPO:probinson[2012-07-25]
OMIM:611131	Retinitis pigmentosa 37		HP:0001133	PMID:17564971	PCS		11/14			P	HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0003621	PMID:17564971	PCS		12/13			C	HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0000662	PMID:17564971	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0000552	OMIM:611131	TAS					P	HPO:skoehler[2013-05-29]
OMIM:611131	Retinitis pigmentosa 37		HP:0000580	OMIM:611131	IEA					P	HPO:iea[2009-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0100018	PMID:17564971	PCS		2/14			P	HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0011462	PMID:17564971	PCS		1/13			C	HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0000613	PMID:17564971	PCS		4/13			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0000007	OMIM:611131	IEA					I	HPO:iea[2009-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0007663	PMID:17564971	PCS		14/14			P	HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0008028	PMID:17564971	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0007787	PMID:17564971	PCS		6/14			P	HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0000642	PMID:17564971	PCS					P	HPO:skoehler[2013-05-29];HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0000510	PMID:17564971	PCS		14/14			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0007688	PMID:17564971	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:611131	Retinitis pigmentosa 37		HP:0000006	PMID:17564971	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:617540	Pituitary adenoma 5, multiple types		HP:0002893	PMID:28413019	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:617540	Pituitary adenoma 5, multiple types		HP:0003581	PMID:28413019	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:617540	Pituitary adenoma 5, multiple types		HP:0003829	PMID:28413019	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:617540	Pituitary adenoma 5, multiple types		HP:0000006	PMID:28413019	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:614049	Atrial fibrillation, familial, 11		HP:0003596	PMID:23348765	PCS		3/3			C	HPO:probinson[2022-07-10]
OMIM:614049	Atrial fibrillation, familial, 11		HP:0005110	PMID:23348765;PMID:20818502;PMID:20650941	PCS		21/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:614049	Atrial fibrillation, familial, 11		HP:0012664	PMID:23348765	PCS		0/2			P	HPO:probinson[2022-07-10]
OMIM:614049	Atrial fibrillation, familial, 11		HP:0006677	PMID:23348765	PCS		1/3			P	HPO:probinson[2022-07-10]
OMIM:614049	Atrial fibrillation, familial, 11		HP:0000006	PMID:20818502	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-10]
OMIM:614049	Atrial fibrillation, familial, 11		HP:0034308	PMID:23348765	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0002465	OMIM:612438	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0003676	OMIM:612438	IEA					C	HPO:skoehler[2010-06-19]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001332	PMID:23582646	PCS		10/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0004322	OMIM:612438	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001272	PMID:23582646	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001250	PMID:23582646	PCS		1/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0002063	PMID:23582646	PCS		9/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001252	PMID:23582646	PCS		2/11			P	HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001251	PMID:23582646	PCS		8/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0006808	OMIM:612438	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0003593	PMID:23582646	PCS		2/11			C	HPO:probinson[2022-12-16];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001270	PMID:23582646	PCS		7/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000639	PMID:23582646	PCS		2/11			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0011463	PMID:23582646	PCS		9/11			C	HPO:probinson[2022-12-16];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001328	OMIM:612438	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000657	PMID:23582646	PCS		2/11			P	HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0003745	OMIM:612438	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0002415	PMID:23582646	PCS		11/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001249	PMID:23582646	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0008936	OMIM:612438	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000252	OMIM:612438	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000571	PMID:23582646	PCS		2/11			P	HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000750	PMID:23582646	PCS		6/11			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001266	PMID:23582646	PCS		5/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0002376	PMID:23582646	PCS		11/11			P	HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001260	PMID:23582646	PCS		11/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000648	OMIM:612438	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000505	PMID:23582646	PCS		1/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001257	PMID:23582646	PCS		11/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0000006	PMID:23582646	PCS					I	HPO:skoehler[2013-09-10];HPO:probinson[2022-12-16]
OMIM:612438	Leukodystrophy, hypomyelinating, 6		HP:0001337	PMID:23582646	PCS		8/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-16]
OMIM:615431	Myopia 23, autosomal recessive		HP:0000007	PMID:23830514	PCS					I	HPO:probinson[2015-05-08]
OMIM:615431	Myopia 23, autosomal recessive		HP:0007663	OMIM:615431	TAS					P	HPO:skoehler[2015-07-26]
OMIM:615431	Myopia 23, autosomal recessive		HP:0000505	PMID:23830514	PCS					P	HPO:probinson[2015-05-08]
OMIM:615431	Myopia 23, autosomal recessive		HP:0011003	PMID:23830514	PCS					P	HPO:probinson[2015-05-08]
OMIM:615431	Myopia 23, autosomal recessive		HP:0007800	PMID:23830514	PCS					P	HPO:probinson[2015-05-08]
OMIM:618115	Spermatogenic failure 32		HP:0011462	PMID:20506135	PCS		2/2			C	HPO:probinson[2023-01-30]
OMIM:618115	Spermatogenic failure 32		HP:0003251	PMID:20506135	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:618115	Spermatogenic failure 32		HP:0034299	PMID:20506135	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:618115	Spermatogenic failure 32		HP:0011961	PMID:20506135	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:618115	Spermatogenic failure 32		HP:0000006	PMID:20506135	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-30]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0001374	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0002021	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0005211	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000656	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0008897	OMIM:263750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000378	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0002558	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000698	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0002974	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000077	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0001760	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000054	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000175	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000494	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000453	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0003022	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000272	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000767	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0002946	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000007	OMIM:263750	IEA					I	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000405	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000625	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0001159	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0001510	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0009778	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000028	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000204	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000347	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0000369	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:263750	Postaxial acrofacial dysostosis		HP:0002984	OMIM:263750	IEA					P	HPO:iea[2009-02-17]
OMIM:616138	Perrault syndrome 5		HP:0001265	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0003236	PMID:25355836	PCS					P	HPO:probinson[2020-08-10]
OMIM:616138	Perrault syndrome 5		HP:0000133	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0003542	OMIM:616138	TAS				HP:0012825	P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0001761	OMIM:616138	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0001250	OMIM:616138	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0002151	OMIM:616138	TAS				HP:0012825	P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0001251	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0003390	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0000815	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0000639	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0000602	OMIM:616138	TAS				HP:0012825	P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0000007	PMID:25355836	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-10]
OMIM:616138	Perrault syndrome 5		HP:0000218	OMIM:616138	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0002403	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616138	Perrault syndrome 5		HP:0000786	OMIM:616138	TAS					P	HPO:skoehler[2015-01-04]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0002663	OMIM:600969	TAS					P	HPO:probinson[2009-02-17]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0003236	PMID:10655510	PCS				HP:0012825	P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0001377	PMID:10090888	PCS		2/8			P	HPO:probinson[2021-02-26]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0003066	PMID:10090888	PCS		4/8			P	HPO:probinson[2021-02-26]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0001384	OMIM:600969	TAS					P	HPO:probinson[2009-02-17]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0010049	OMIM:600969	TAS					P	HPO:probinson[2009-02-17]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0030839	PMID:10090888	PCS		6/8			P	HPO:probinson[2021-02-26]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0010585	OMIM:600969	TAS					P	HPO:probinson[2012-06-18]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0008180	OMIM:600969	TAS					P	HPO:skoehler[2015-12-30]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0010582	OMIM:600969	TAS					P	HPO:probinson[2012-06-18]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0002758	OMIM:600969	TAS					P	HPO:skoehler[2010-06-18]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0002656	OMIM:600969	TAS					P	HPO:probinson[2009-02-17]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0003701	PMID:10655510	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0000006	PMID:10090888	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:600969	Epiphyseal dysplasia, multiple, 3, with or without myopathy		HP:0003502	OMIM:600969	TAS					P	HPO:probinson[2009-02-17]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0002069	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0001298	PMID:37191094	PCS		8/8		HP:0033184	P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0003577	PMID:36935417	PCS		1/2			C	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0003621	PMID:37191094	PCS		1/8			C	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0002870	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0025313	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0011968	PMID:36935417	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0000160	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0002572	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0001252	PMID:36935417	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0003593	PMID:37191094	PCS		4/8			C	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0002093	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0032988	PMID:36935417	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0007281	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0000518	PMID:36935417	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0011463	PMID:37191094	PCS		3/8			C	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0000007	PMID:36935417	PCS					I	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0020221	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0002788	PMID:36935417	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620461	Encephalopathy, acute, infection-induced, susceptibility to, 12		HP:0007359	PMID:36935417	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:249620	Ohdo syndrome		HP:0000286	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000365	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000343	OMIM:249620	TAS					P	HPO:probinson[2012-05-01]
OMIM:249620	Ohdo syndrome		HP:0000046	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000463	OMIM:249620	TAS					P	HPO:probinson[2013-04-09]
OMIM:249620	Ohdo syndrome		HP:0004322	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0001250	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000160	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000581	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0001252	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0003196	OMIM:249620	TAS					P	HPO:probinson[2013-04-09]
OMIM:249620	Ohdo syndrome		HP:0001290	OMIM:249620	TAS					P	HPO:skoehler[2017-07-13]
OMIM:249620	Ohdo syndrome		HP:0045075	OMIM:249620	TAS					P	HPO:probinson[2022-05-07]
OMIM:249620	Ohdo syndrome		HP:0000319	OMIM:249620	TAS					P	HPO:probinson[2012-05-01]
OMIM:249620	Ohdo syndrome		HP:0008551	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0030680	OMIM:249620	TAS					P	HPO:probinson[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0008872	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0001249	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0001760	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000233	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000431	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0001382	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000093	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0005280	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000508	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0004209	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000685	OMIM:249620	IEA					P	HPO:skoehler[2015-12-30]
OMIM:249620	Ohdo syndrome		HP:0000006	OMIM:249620	IEA					I	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000028	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000347	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000402	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:249620	Ohdo syndrome		HP:0000687	OMIM:249620	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0006747	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0011979	OMIM:256700	TAS					P	HPO:probinson[2012-07-18]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0001251	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0011976	OMIM:256700	TAS					P	HPO:probinson[2012-07-18]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0010543	OMIM:256700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0011977	OMIM:256700	TAS					P	HPO:probinson[2012-07-18]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0011978	OMIM:256700	TAS					P	HPO:probinson[2012-07-18]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0031500	OMIM:256700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0033823	OMIM:256700	TAS					P	HPO:probinson[2022-06-14];HPO:probinson[2022-06-14]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0011281	OMIM:256700	TAS					P	HPO:probinson[2012-07-16]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0001508	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0001903	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0003829	OMIM:256700	IEA					I	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0001945	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0001824	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0003745	OMIM:256700	IEA					I	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0003006	OMIM:256700	TAS					P	HPO:probinson[2012-07-16]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0002014	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0002653	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0003005	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0002277	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0001442	OMIM:256700	IEA					I	HPO:skoehler[2019-04-18]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0002176	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0000822	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0200036	OMIM:256700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0002027	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0000006	OMIM:256700	IEA					I	HPO:iea[2009-02-17]
OMIM:256700	Neuroblastoma, susceptibility to		HP:0001336	OMIM:256700	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0000365	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0000486	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0002376	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0001272	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0001250	PMID:15548604	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0002352	PMID:15548604	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-01-16]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0002283	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0001285	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0003593	PMID:15548604	PCS		5/5			C	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0001251	PMID:15548604	PCS		5/5			P	HPO:probinson[2023-01-16]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0002171	OMIM:236792	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0002381	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0002062	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0002071	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0040147	OMIM:236792	IEA					P	HPO:skoehler[2015-01-27]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0007371	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0000639	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0040144	PMID:15548604	PCS		5/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-01-16]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0007256	OMIM:236792	TAS					P	HPO:skoehler[2015-01-04]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0000007	PMID:15548604	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0000648	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0007258	OMIM:236792	IEA					P	HPO:iea[2009-02-17]
OMIM:236792	L-2-hydroxyglutaric aciduria		HP:0001249	PMID:15548604	PCS		5/5			P	HPO:probinson[2023-01-16]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0000252	PMID:30723320	PCS		3/11			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0000054	PMID:30723320	PCS		1/6			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0003577	PMID:30723320	PCS		10/11			C	HPO:probinson[2022-04-30]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0000750	PMID:30723320	PCS		9/11			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0001596	PMID:30723320	PCS		11/11			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0031936	PMID:30723320	PCS					P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0002079	PMID:30723320	PCS		3/10			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0001250	PMID:30723320	PCS	HP:0003623	7/11			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0008064	PMID:30723320	PCS					P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0000729	PMID:30723320	PCS					P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0000007	PMID:30723320	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0001019	PMID:30723320	PCS					P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0000713	PMID:30723320	PCS		1/11			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0000047	PMID:30723320	PCS		2/6	MALE		P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0008689	PMID:30723320	PCS		1/6			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0001249	PMID:30723320	PCS		11/11			P	HPO:probinson[2020-07-23]
OMIM:618840	Alopecia-intellectual disability syndrome 4		HP:0003623	PMID:30723320	PCS		1/11			C	HPO:probinson[2022-04-30]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0012377	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0001250	PMID:11835386	PCS		1/5			P	HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0002352	PMID:11835386;PMID:21484434	PCS		3/3			P	HPO:probinson[2023-06-27];HPO:probinson[2023-06-27];HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0001260	PMID:11835386	PCS		1/5			P	HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0000869	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0007340	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0011462	PMID:21484434	PCS		1/1			C	HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0000007	PMID:11835386	PCS					I	HPO:probinson[2023-06-27]
OMIM:620313	Leukoencephalopathy with vanishing white matter 3, with or without ovarian failure		HP:0002505	PMID:11835386	PCS		4/5			P	HPO:probinson[2023-06-27]
OMIM:217990	Corpus callosum, agenesis of		HP:0012385	OMIM:217990	TAS					P	HPO:skoehler[2013-10-22]
OMIM:217990	Corpus callosum, agenesis of		HP:0000252	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0000384	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0009473	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0001274	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0011220	OMIM:217990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0000007	OMIM:217990	IEA					I	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0002007	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0000256	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0001510	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:217990	Corpus callosum, agenesis of		HP:0001249	OMIM:217990	IEA					P	HPO:iea[2009-02-17]
OMIM:216330	Cleidocranial dysplasia, recessive form		HP:0003510	OMIM:216330	IEA					P	HPO:iea[2009-02-17]
OMIM:216330	Cleidocranial dysplasia, recessive form		HP:0000007	OMIM:216330	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:216330	Cleidocranial dysplasia, recessive form		HP:0000248	OMIM:216330	IEA					P	HPO:iea[2009-02-17]
OMIM:128500	Ear folding		HP:0000598	OMIM:128500	IEA					P	HPO:iea[2009-02-17]
OMIM:128500	Ear folding		HP:0000006	OMIM:128500	IEA					I	HPO:iea[2009-02-17]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000286	PMID:30315159	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000582	PMID:30315159	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0003577	PMID:30315159	PCS		2/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000365	PMID:30315159	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0001250	PMID:30315159	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0003593	PMID:30315159;PMID:30733661	PCS		5/7			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0002061	PMID:30315159	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0011877	PMID:30315159	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0002282	PMID:30733661	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:4000170	PMID:30315159	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0032438	PMID:30315159	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0011342	PMID:30315159	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0008551	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0001845	PMID:30315159;PMID:30733661	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000414	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000219	PMID:30315159	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000218	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000455	PMID:30315159	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0001643	PMID:30315159	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000358	PMID:30315159;PMID:30733661	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000154	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000396	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0001561	PMID:30733661	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000431	PMID:30315159;PMID:30733661	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0005487	PMID:30733661	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000490	PMID:30315159;PMID:30733661	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0011800	PMID:30315159;PMID:30733661	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0011229	PMID:30315159	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0011228	PMID:30315159	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000506	PMID:30315159;PMID:30733661	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0001537	PMID:30315159;PMID:30733661	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000527	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000307	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0004308	PMID:30733661	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000664	PMID:30315159	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0001873	PMID:30315159	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000303	PMID:30315159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620475	Thrombocytopenia 8, with dysmorphic features and developmental delay		HP:0000006	PMID:30315159	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603284	Cerebral cavernous malformations 2		HP:0001342	OMIM:603284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603284	Cerebral cavernous malformations 2		HP:0001297	OMIM:603284	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603284	Cerebral cavernous malformations 2		HP:0001250	OMIM:603284	IEA					P	HPO:iea[2009-02-17]
OMIM:603284	Cerebral cavernous malformations 2		HP:0001009	OMIM:603284	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603284	Cerebral cavernous malformations 2		HP:0033522	PMID:21543988	PCS		3/3			P	HPO:probinson[2021-04-14]
OMIM:603284	Cerebral cavernous malformations 2		HP:0002315	OMIM:603284	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603284	Cerebral cavernous malformations 2		HP:0000006	PMID:9811928	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-04-14]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0001276	PMID:31724321	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0001583	PMID:22581968	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0003621	PMID:31724321	PCS		1/1			C	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000486	PMID:31724321	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0002353	PMID:22581968	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000034	OMIM:614920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0002076	PMID:31724321	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0001271	PMID:22581968	PCS					P	HPO:skoehler[2013-01-11]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000020	OMIM:614920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0001284	OMIM:614920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000639	PMID:31724321	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000958	OMIM:614920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0007099	PMID:22581968	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000519	PMID:31724321;PMID:22581968	PCS		2/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000007	PMID:22581968	PCS					I	HPO:skoehler[2013-01-09]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0002505	PMID:22581968	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0001324	OMIM:614920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0001730	PMID:22581968	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0000545	PMID:31724321	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0001249	PMID:31724321	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614920	Peroxisome biogenesis disorder 14B		HP:0002522	PMID:22581968	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002169	PMID:20952379	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0003577	PMID:18711368;PMID:23562994;PMID:20952379	PCS		5/5			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-12];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0000340	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001332	PMID:18711368;PMID:20952379	PCS		3/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002365	PMID:23562994	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001272	OMIM:612389	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001250	OMIM:612389;PMID:20952379	PCS		12/13			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001252	OMIM:612389	TAS					P	HPO:skoehler[2015-02-22]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0032794	PMID:23562994	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0100704	PMID:20952379	PCS		2/2			P	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0000954	PMID:23562994	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002119	OMIM:612389	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001522	PMID:20952379	PCS		1/3			C	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0008936	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001320	PMID:23562994	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002179	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0000253	PMID:20952379	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002059	OMIM:612389	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002015	PMID:20952379	PCS		2/3			P	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0007308	PMID:20952379	PCS		2/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0000252	PMID:18711368;PMID:23562994	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001561	PMID:18711368	PCS		0/1			P	HPO:probinson[2022-09-12];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0003487	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001321	PMID:23562994	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002079	OMIM:612389	TAS					P	HPO:skoehler[2015-02-22]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0011968	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002033	PMID:23562994	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002072	PMID:18711368	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0003819	PMID:20952379	PCS		2/3			C	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0032792	PMID:23562994	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0002509	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0000007	PMID:18711368	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0000505	PMID:18711368	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0001257	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:612389	Pontocerebellar hypoplasia, type 2B		HP:0009879	PMID:23562994	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-12]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0002014	OMIM:600955	IEA					P	HPO:iea[2009-02-17]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0000044	PMID:9207799	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-09]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0008163	PMID:9207799	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-09]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0002024	OMIM:600955	IEA					P	HPO:iea[2009-02-17]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0012051	OMIM:600955	TAS					P	HPO:probinson[2009-02-17]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0011463	PMID:9207799	PCS		1/1			C	HPO:probinson[2023-06-09]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0011473	OMIM:600955	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0000007	PMID:9207799	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-09]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0040216	PMID:9207799	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:6000419	PMID:9207799	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0001513	PMID:9207799	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-09]
OMIM:600955	Proprotein convertase 1/3 deficiency		HP:0000786	OMIM:600955	IEA					P	HPO:iea[2009-02-17]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0003581	PMID:14662268	PCS					C	HPO:probinson[2022-07-04]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0030682	OMIM:601493	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0001635	OMIM:601493	IEA					P	HPO:skoehler[2010-06-19]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0001712	PMID:14662268	PCS		8/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-04]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0006685	OMIM:601493	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0011713	PMID:14662268	PCS		1/13			P	HPO:probinson[2022-07-04]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0004308	OMIM:601493	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0033755	PMID:14662268	PCS		10/13			P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0000006	PMID:14662268	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-04]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0001645	PMID:14662268	PCS		3/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-04]
OMIM:601493	Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction		HP:0001644	PMID:14662268	PCS		13/13			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-07-04]
OMIM:301116	Intellectual developmental disorder, X-linked 113		HP:0000750	PMID:32816001	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:301116	Intellectual developmental disorder, X-linked 113		HP:0011463	PMID:32816001	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:301116	Intellectual developmental disorder, X-linked 113		HP:0001419	PMID:32816001	PCS					I	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:301116	Intellectual developmental disorder, X-linked 113		HP:0001270	PMID:32816001	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-26]
OMIM:117900	Cervical rib		HP:0000891	OMIM:117900	IEA					P	HPO:iea[2009-02-17]
OMIM:117900	Cervical rib		HP:0000707	OMIM:117900	IEA					P	HPO:iea[2009-02-17]
OMIM:117900	Cervical rib		HP:0000006	OMIM:117900	IEA					I	HPO:iea[2009-02-17]
OMIM:616851	Cataract 45		HP:0000519	PMID:25804400	PCS	HP:0003577				P	HPO:probinson[2017-06-23]
OMIM:616851	Cataract 45		HP:0000007	PMID:25804400	PCS					I	HPO:probinson[2017-06-23]
OMIM:129150	Echo virus 11 sensitivity		HP:0002715	OMIM:129150	IEA					P	HPO:iea[2009-02-17]
OMIM:129150	Echo virus 11 sensitivity		HP:0000006	OMIM:129150	IEA					I	HPO:iea[2009-02-17]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0003577	PMID:26148990	PCS		1/4			C	HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0001894	PMID:26148990	PCS		2/4			P	HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0002240	OMIM:616689	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0003593	PMID:26148990	PCS		1/4			C	HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0011463	PMID:26148990	PCS		2/4			C	HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0002904	OMIM:616689	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0001927	PMID:26148990	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0001878	PMID:26148990	PCS	HP:0003577	4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0025548	PMID:26148990	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0020122	PMID:26148990	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0005518	PMID:26148990	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0001923	PMID:26148990	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0004823	PMID:26148990	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0000006	PMID:26148990	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-08]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0000952	OMIM:616689	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616689	Dehydrated hereditary stomatocytosis 2		HP:0001744	PMID:26148990	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:400047	DEAFNESS, Y-LINKED 2		HP:0000407	OMIM:400047	IEA					P	HPO:skoehler[2019-09-07]
OMIM:400047	DEAFNESS, Y-LINKED 2		HP:0001450	PMID:30341416	TAS					I	HPO:nvasilevsky[2019-09-11]
OMIM:257350	Nuchal bleb, familial		HP:0003826	OMIM:257350	TAS					C	HPO:probinson[2014-01-01]
OMIM:257350	Nuchal bleb, familial		HP:0000007	OMIM:257350	TAS					I	HPO:skoehler[2009-02-17]
OMIM:257350	Nuchal bleb, familial		HP:0001789	OMIM:257350	TAS					P	HPO:skoehler[2009-02-17]
OMIM:257350	Nuchal bleb, familial		HP:0010878	OMIM:257350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:257350	Nuchal bleb, familial		HP:0000476	OMIM:257350	TAS					P	HPO:skoehler[2010-06-20]
OMIM:609965	Deafness, autosomal dominant 53		HP:0003621	PMID:15958501	PCS					C	HPO:probinson[2024-03-14];HPO:probinson[2024-03-14]
OMIM:609965	Deafness, autosomal dominant 53		HP:0001751	PMID:15958501	PCS		0/6			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-14]
OMIM:609965	Deafness, autosomal dominant 53		HP:0025708	PMID:15958501	PCS					C	HPO:probinson[2024-03-14];HPO:probinson[2024-03-14]
OMIM:609965	Deafness, autosomal dominant 53		HP:0000407	PMID:15958501	PCS	HP:0003621	16/16			P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:609965	Deafness, autosomal dominant 53		HP:0000006	PMID:15958501	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0002169	PMID:31855247	PCS		2/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0002015	PMID:31855247	PCS		4/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0000750	PMID:31855247	PCS		2/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0000486	PMID:31855247	PCS		3/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0002353	PMID:31855247	PCS		1/4			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0001332	PMID:31855247	PCS		2/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0003487	PMID:31855247	PCS		3/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0002373	PMID:31855247	PCS		1/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0001272	PMID:31855247	PCS		3/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0001260	PMID:31855247	PCS		4/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0000020	PMID:31855247	PCS		4/4			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0002073	PMID:31855247	PCS		4/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0033048	PMID:31855247	PCS		2/5			P	HPO:probinson[2020-08-13]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0033049	PMID:31855247	PCS		2/5			P	HPO:probinson[2020-08-13]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0002607	PMID:31855247	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0000514	PMID:31855247	PCS		4/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0000007	PMID:31855247	PCS					I	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0000648	PMID:31855247	PCS		4/4			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0001268	PMID:31855247	PCS		4/5			P	HPO:probinson[2020-07-10]
OMIM:618868	Neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline		HP:0006579	PMID:31855247	PCS	HP:0003623	2/5			P	HPO:probinson[2020-07-10]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0000473	OMIM:611694	IEA					P	HPO:iea[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0002015	OMIM:611694	IEA					P	HPO:iea[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0007979	OMIM:611694	TAS					P	HPO:skoehler[2013-05-31]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0001332	OMIM:611694	TAS					P	HPO:probinson[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0012179	OMIM:611694	TAS					P	HPO:probinson[2013-02-24]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0001272	OMIM:611694	IEA					P	HPO:iea[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0001618	OMIM:611694	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0001260	OMIM:611694	IEA					P	HPO:iea[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0000007	OMIM:611694	TAS					I	HPO:probinson[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0002073	OMIM:611694	IEA					P	HPO:iea[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0001348	OMIM:611694	IEA					P	HPO:iea[2009-02-17]
OMIM:611694	Dystonia with cerebellar atrophy		HP:0000478	OMIM:611694	IEA					P	HPO:iea[2009-02-17]
OMIM:620449	Immunodeficiency 112		HP:0002850	PMID:25406581;PMID:29230214	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0005403	PMID:25406581;PMID:29230214	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0002783	PMID:25406581	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0030388	PMID:25406581	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0020086	PMID:25406581;PMID:29230214	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0020087	PMID:25406581;PMID:29230214	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0003593	PMID:25406581	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0010976	PMID:25406581;PMID:29230214	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0500271	PMID:29230214	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0011463	PMID:25406581;PMID:29230214	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0002728	PMID:25406581	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0002718	PMID:25406581;PMID:29230214	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0100828	PMID:25406581;PMID:29230214	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0000007	PMID:25406581	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0004429	PMID:25406581;PMID:29230214	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0002720	PMID:25406581;PMID:29230214	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0004315	PMID:25406581;PMID:29230214	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0040218	PMID:25406581;PMID:29230214	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0005404	PMID:25406581;PMID:29230214	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620449	Immunodeficiency 112		HP:0002028	PMID:25406581	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614934	Deafness, autosomal recessive 70		HP:0000365	PMID:23084290	PCS	HP:0011463	3/3		HP:0012832	P	HPO:skoehler[2013-06-06];HPO:probinson[2020-08-09]
OMIM:614934	Deafness, autosomal recessive 70		HP:0001751	PMID:23084290	PCS		0/3			P	HPO:probinson[2020-08-09];HPO:probinson[2022-08-23]
OMIM:614934	Deafness, autosomal recessive 70		HP:0100543	PMID:23084290	PCS		0/3			P	HPO:probinson[2020-08-09];HPO:probinson[2022-08-23]
OMIM:614934	Deafness, autosomal recessive 70		HP:0011463	PMID:23084290	PCS		3/3			C	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:614934	Deafness, autosomal recessive 70		HP:0000007	PMID:23084290	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2020-08-09]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0033605	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:6000374	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0003493	PMID:38652464	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0003593	PMID:38630025	PCS		1/2			C	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0010783	PMID:38630025;PMID:38652464	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0032435	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0011897	PMID:38630025	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0012311	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0001945	PMID:38630025;PMID:38652464	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0012490	PMID:38630025	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0002615	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0004315	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0025615	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0003623	PMID:38630025;PMID:38652464	PCS		2/3			C	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0001880	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0002098	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0030783	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0012219	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0012115	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0011227	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0100584	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0000969	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0032252	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0100537	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0002923	PMID:38652464	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0001510	PMID:38652464	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0001873	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0002720	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0000006	PMID:38630025	PCS					I	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621030	Autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant		HP:0001974	PMID:38630025	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0001265	OMIM:607791	IEA					P	HPO:probinson[2009-02-17]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0003378	OMIM:607791	IEA					P	HPO:probinson[2009-02-17]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0003693	OMIM:607791	TAS					P	HPO:probinson[2009-02-17]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0003484	OMIM:607791	IEA					P	HPO:probinson[2012-03-13]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0001284	OMIM:607791	IEA					P	HPO:probinson[2009-02-17]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0002460	OMIM:607791	TAS					P	HPO:probinson[2013-12-15]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0002936	OMIM:607791	IEA					P	HPO:probinson[2009-02-17]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0003481	OMIM:607791	TAS					P	HPO:probinson[2014-01-01]
OMIM:607791	Charcot-Marie-Tooth disease, dominant intermediate D		HP:0000006	OMIM:607791	IEA					I	HPO:probinson[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001298	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001252	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001251	PMID:15122711	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0003593	PMID:15122711	PCS		1/3			C	HPO:probinson[2012-03-18];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001290	OMIM:203700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0003470	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001408	PMID:15122711	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0011463	PMID:15122711	PCS		2/3			C	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002779	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0012072	OMIM:203700	TAS					P	HPO:skoehler[2012-11-21]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0006554	PMID:15122711	PCS		2/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0000952	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0000572	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001541	PMID:15122711	PCS		2/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002791	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001263	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002151	PMID:15122711	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002273	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0031358	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0000649	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0000726	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0000007	PMID:15122711	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001414	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001413	PMID:15122711	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001336	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0003678	PMID:15122711	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001276	PMID:15122711	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001399	PMID:15122711	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001272	PMID:15122711	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002240	OMIM:203700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0012847	PMID:15122711	PCS		1/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0000939	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0001508	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0100704	PMID:15122711	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0011166	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0012050	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002910	PMID:15122711	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002059	PMID:15122711	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002650	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002133	PMID:15122711	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002376	OMIM:203700	PCS					P	HPO:probinson[2012-03-18]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002013	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0032860	PMID:15122711	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002171	PMID:15122711	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002529	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0003219	OMIM:203700	TAS					P	HPO:skoehler[2012-11-21]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002922	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0006964	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0003535	OMIM:203700	TAS					P	HPO:skoehler[2012-11-21]
OMIM:203700	Mitochondrial DNA depletion syndrome 4A (Alpers type)		HP:0002446	OMIM:203700	IEA					P	HPO:iea[2009-02-17]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0031956	PMID:23315540	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0001639	PMID:23315540	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0002151	PMID:23315540	PCS		1/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0003593	PMID:23315540	PCS		2/2			C	HPO:skoehler[2013-09-30];HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0000007	PMID:23315540	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0001522	PMID:23315540	PCS		1/2			C	HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0001414	PMID:23315540	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0031964	PMID:23315540	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:615395	Combined oxidative phosphorylation deficiency 16		HP:0003688	PMID:23315540	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0001696	PMID:23122589	PCS		2/6			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0002110	PMID:23122589	PCS		4/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0003251	PMID:23122589	PCS		5/5			P	HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0100582	PMID:23122589	PCS		2/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0011108	PMID:23122589	PCS		5/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0012259	PMID:23122589	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0200073	PMID:23122589	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0012265	PMID:23122589	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0012263	PMID:23122589;PMID:23891469	PCS		12/12			P	HPO:probinson[2013-04-07];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0012384	PMID:23122589	PCS		5/6		HP:0031796	P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0000007	PMID:23122589	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0000403	PMID:23122589	PCS		3/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0002205	PMID:23891469	PCS					P	HPO:skoehler[2012-12-02];HPO:probinson[2022-03-20]
OMIM:614935	Ciliary dyskinesia, primary, 19		HP:0004469	PMID:23122589	PCS		5/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-03-20]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:6000461	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0002312	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0002015	PMID:37143309	PCS		0/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0002133	PMID:37143309	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0001332	PMID:37143309	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0001250	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0002066	PMID:37143309	PCS		0/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0001260	PMID:37143309	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0001263	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0002063	PMID:37143309	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0003593	PMID:37143309	PCS		2/2			C	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0100710	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0000752	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0000256	PMID:37143309	PCS	HP:0003593	2/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0001257	PMID:37143309	PCS		0/2			P	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0000006	PMID:37143309	PCS					I	HPO:probinson[2024-03-02]
OMIM:620448	Megalencephalic leukoencephalopathy with subcortical cysts 4, remitting		HP:0001249	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0003577	PMID:16783569	PCS		2/3			C	HPO:probinson[2023-03-12];HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0000023	PMID:16783569	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0002783	PMID:16783569	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0001162	PMID:16783569	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0001263	PMID:16783569	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0001252	PMID:16783569	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0003593	PMID:16783569	PCS		1/3			C	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0011304	PMID:16783569	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0009381	PMID:16783569	PCS		2/3			P	HPO:probinson[2013-04-09]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0001419	PMID:16783569	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0002119	PMID:16783569	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0000218	PMID:16783569	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0002205	PMID:16783569	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0002788	PMID:16783569	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0000256	PMID:16783569	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0000369	PMID:16783569	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0002643	PMID:16783569	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:300209	Simpson-Golabi-Behmel syndrome, type 2		HP:0001513	PMID:16783569	PCS		1/3			P	HPO:skoehler[2019-04-18]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0000176	PMID:8793927	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0003621	PMID:8793927;PMID:21559944	PCS		3/4			C	HPO:probinson[2022-05-29];HPO:probinson[2022-03-31]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0004322	PMID:8793927	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0030840	PMID:21559944	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0000193	PMID:8793927	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0030839	PMID:21559944	PCS		3/3			P	HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0030838	PMID:21559944	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0005072	PMID:21559944	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0005280	PMID:8793927	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:6000969	PMID:8793927	PCS		1/1			P	HPO:probinson[2024-08-04]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0032072	PMID:8793927	PCS		1/1			P	HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0006094	PMID:21559944	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0100769	PMID:21559944	PCS		3/3			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0010485	PMID:21559944	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0011463	PMID:21559944	PCS		1/3			C	HPO:probinson[2022-05-29]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0033640	PMID:8793927	PCS		1/1			P	HPO:probinson[2021-04-16]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0000403	PMID:8793927	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0000007	PMID:10339581	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0000934	PMID:8793927	PCS		1/1			P	HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0020127	PMID:8793927	PCS		1/1			P	HPO:probinson[2021-02-19]
OMIM:601492	Mucopolysaccharidosis type IX		HP:0004626	PMID:21559944	PCS		1/3			P	HPO:probinson[2022-05-29]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001397	PMID:24499211;PMID:33342467	PCS		9/30			P	HPO:probinson[2021-10-17];HPO:skoehler[2014-07-11];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0002047	PMID:24499211	PCS		2/19			P	HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0003236	PMID:24499211;PMID:22492991;PMID:33342467	PCS		19/32			P	HPO:probinson[2021-10-17];HPO:skoehler[2012-11-25];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0031628	PMID:24499211	PCS		2/19			P	HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0004322	PMID:24499211	PCS		15/19			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0030353	PMID:33342467	PCS		3/9			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001252	PMID:33342467	PCS		3/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0002240	PMID:33342467	PCS		2/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001270	PMID:33342467	PCS		3/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0031964	PMID:33342467	PCS		11/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0008151	PMID:33342467	PCS		4/10			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001629	PMID:33342467	PCS		2/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001943	PMID:24499211;PMID:33342467	PCS		21/21		HP:0025303	P	HPO:probinson[2021-10-17];HPO:skoehler[2014-07-11];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001649	PMID:22492991	PCS		1/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0200123	PMID:22492991	PCS		1/2			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001406	PMID:24499211	PCS		2/19			P	HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001324	PMID:24499211	PCS		2/19			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0002910	PMID:24499211;PMID:22492991	PCS		21/21			P	HPO:probinson[2021-10-17];HPO:skoehler[2012-11-25];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001645	PMID:24499211	PCS		2/19			P	HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0005305	PMID:22492991	PCS		1/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001644	PMID:24499211;PMID:22492991	PCS		8/21			P	HPO:probinson[2021-10-17];HPO:skoehler[2012-11-25];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0003546	PMID:24499211;PMID:33342467	PCS		9/30			P	HPO:probinson[2021-10-17];HPO:skoehler[2014-07-11];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0003645	PMID:33342467	PCS		5/10			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000175	PMID:24499211;PMID:22492991;PMID:33342467	PCS		25/32			P	HPO:probinson[2021-10-17];HPO:skoehler[2012-11-25];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0031956	PMID:33342467	PCS		11/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0003201	PMID:24499211;PMID:33342467	PCS		7/30			P	HPO:probinson[2021-10-17];HPO:skoehler[2014-07-11];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001640	PMID:33342467	PCS		2/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0002013	PMID:33342467	PCS		1/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000193	PMID:24499211;PMID:33342467	PCS		17/30			P	HPO:probinson[2021-10-17];HPO:skoehler[2014-07-11];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000592	PMID:33342467	PCS		2/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001263	PMID:33342467	PCS		1/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001680	PMID:33342467	PCS		1/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0002094	PMID:22492991	PCS		1/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0002092	PMID:33342467	PCS		2/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0003160	PMID:24499211	PCS					P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0012378	PMID:22492991;PMID:33342467	PCS		3/13			P	HPO:probinson[2021-10-17];HPO:skoehler[2013-10-22];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0012115	PMID:33342467	PCS		2/11		HP:0011010	P	HPO:skoehler[2014-07-11];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000007	PMID:19625727	PCS					I	HPO:skoehler[2012-11-25];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000403	PMID:33342467	PCS		1/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001976	PMID:22492991;PMID:33342467	PCS		2/13			P	HPO:probinson[2021-10-17];HPO:skoehler[2012-11-25];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000823	PMID:24499211	PCS		2/19			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000201	PMID:24499211;PMID:22492991;PMID:33342467	PCS		16/32			P	HPO:probinson[2021-10-17];HPO:skoehler[2012-11-25];HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0001510	PMID:33342467	PCS		10/10			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0006568	PMID:24499211	PCS		2/19			P	HPO:probinson[2021-02-25]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000347	PMID:33342467	PCS		1/11			P	HPO:skoehler[2012-11-25];HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0002028	PMID:33342467	PCS		2/11			P	HPO:probinson[2021-10-17]
OMIM:614921	Congenital disorder of glycosylation, type It		HP:0000126	PMID:33342467	PCS		1/11			P	HPO:probinson[2021-10-17]
OMIM:603285	Cerebral cavernous malformations 3		HP:0001342	PMID:17041941	PCS		15/28			P	HPO:skoehler[2013-01-14];HPO:probinson[2022-01-23]
OMIM:603285	Cerebral cavernous malformations 3		HP:0003621	PMID:17041941	PCS					C	HPO:probinson[2022-01-23]
OMIM:603285	Cerebral cavernous malformations 3		HP:0001250	PMID:17041941	PCS		10/28			P	HPO:skoehler[2013-01-14];HPO:probinson[2022-01-23]
OMIM:603285	Cerebral cavernous malformations 3		HP:0003470	OMIM:603285	IEA		HP:0040282			P	HPO:skoehler[2013-01-14]
OMIM:603285	Cerebral cavernous malformations 3		HP:0033522	PMID:17041941	PCS					P	HPO:probinson[2022-01-23]
OMIM:603285	Cerebral cavernous malformations 3		HP:0002315	PMID:17041941	PCS		HP:0040282			P	HPO:skoehler[2013-01-14];HPO:probinson[2022-01-23]
OMIM:603285	Cerebral cavernous malformations 3		HP:0000006	PMID:17041941	PCS					I	HPO:probinson[2020-11-26];HPO:probinson[2022-01-23]
OMIM:303700	Blue cone monochromacy		HP:0000639	OMIM:303700	PCS		HP:0040282			P	HPO:probinson[2012-04-06]
OMIM:303700	Blue cone monochromacy		HP:0007939	OMIM:303700	PCS					P	HPO:probinson[2012-04-06]
OMIM:303700	Blue cone monochromacy		HP:0001419	OMIM:303700	PCS					I	HPO:probinson[2012-04-06]
OMIM:303700	Blue cone monochromacy		HP:0008002	OMIM:303700	PCS		HP:0040283			P	HPO:probinson[2012-04-06]
OMIM:303700	Blue cone monochromacy		HP:0012043	OMIM:303700	TAS					P	HPO:skoehler[2015-12-30]
OMIM:303700	Blue cone monochromacy		HP:0000613	OMIM:303700	PCS					P	HPO:probinson[2012-04-06]
OMIM:303700	Blue cone monochromacy		HP:0007663	OMIM:303700	TAS					P	HPO:skoehler[2015-07-26]
OMIM:303700	Blue cone monochromacy		HP:0000505	OMIM:303700	PCS					P	HPO:probinson[2012-04-06]
OMIM:303700	Blue cone monochromacy		HP:0000545	OMIM:303700	PCS					P	HPO:probinson[2012-04-06]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0003676	OMIM:613096	IEA					C	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0002166	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0000012	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0001761	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0003487	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0000020	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0002064	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0002061	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0011402	OMIM:613096	TAS					P	HPO:probinson[2012-04-25]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0007340	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0007220	OMIM:613096	TAS					P	HPO:probinson[2012-04-25]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0001258	OMIM:613096	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0000763	OMIM:613096	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0000006	OMIM:613096	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613096	Spastic paraplegia 36, autosomal dominant		HP:0001347	OMIM:613096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0001397	PMID:23770608	PCS		2/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000320	PMID:23770608	PCS		4/4			P	HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000160	OMIM:615381	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0002240	PMID:23770608	PCS		1/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0031964	PMID:23770608	PCS		3/4			P	HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000819	PMID:23770608	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000939	PMID:23770608	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000855	PMID:23770608	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000678	PMID:23770608	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0009125	PMID:23770608	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0002910	OMIM:615381	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0001620	PMID:23770608	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0004334	OMIM:615381	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0002155	PMID:23770608	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0002650	PMID:23770608	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0100585	PMID:23770608	PCS		4/4			P	HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0034392	PMID:23770608	PCS		4/4			P	HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0002808	PMID:23770608	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000407	PMID:23770608	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0100679	PMID:23770608	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000444	OMIM:615381	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0003635	PMID:23770608	PCS		4/4			P	HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000026	PMID:23770608	PCS		3/3			P	HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000520	OMIM:615381	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000006	PMID:23770608	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000028	PMID:23770608	PCS		3/3	MALE		P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:615381	Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome		HP:0000347	PMID:23770608	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-21]
OMIM:605192	Deafness, autosomal dominant 23		HP:0004467	OMIM:605192	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:605192	Deafness, autosomal dominant 23		HP:0000076	OMIM:605192	TAS					P	HPO:skoehler[2015-12-30]
OMIM:605192	Deafness, autosomal dominant 23		HP:0000407	PMID:10777717	PCS					P	HPO:probinson[2013-02-23]
OMIM:605192	Deafness, autosomal dominant 23		HP:0000405	PMID:10777717	PCS		HP:0040282			P	HPO:probinson[2013-02-23]
OMIM:605192	Deafness, autosomal dominant 23		HP:0000006	PMID:10777717	PCS					I	HPO:probinson[2013-01-09]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0001320	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0004467	OMIM:101805	TAS					P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000252	PMID:25945454	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000494	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000175	PMID:25945454	PCS		0/1			P	HPO:nvasilevsky[2019-09-09];HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000670	OMIM:101805	TAS					P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0004279	OMIM:101805	TAS					P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0004322	PMID:25945454	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0002079	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0001156	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0002120	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0003298	PMID:25945454	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0005321	OMIM:101805	IEA					P	HPO:skoehler[2019-09-07]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000272	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0002280	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000349	OMIM:101805	TAS					P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000954	PMID:25945454	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000448	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0001511	OMIM:101805	TAS					P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000465	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000047	OMIM:101805	TAS					P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000347	PMID:25945454	PCS		1/1			P	HPO:probinson[2024-03-06]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000028	OMIM:101805	TAS					P	HPO:skoehler[2017-07-13]
OMIM:101805	Acrofacial dysostosis, Catania type		HP:0000006	OMIM:101805	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001276	OMIM:616688	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003431	PMID:7964809	PCS		4/4			P	HPO:probinson[2022-07-17];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0000365	OMIM:616688	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003693	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002066	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001252	OMIM:616688	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003394	OMIM:616688	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0000020	OMIM:616688	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001251	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002460	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002380	OMIM:616688	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0031189	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001270	OMIM:616688	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001171	OMIM:616688	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0011462	PMID:7964809	PCS		2/4			C	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0009027	PMID:7964809	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002936	PMID:7964809	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0008954	PMID:7964809	PCS		2/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003701	OMIM:616688	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001620	OMIM:616688	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001763	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001265	PMID:7964809	PCS		2/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002311	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002312	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003621	PMID:7964809	PCS		2/4			C	HPO:probinson[2022-07-17];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002411	OMIM:616688	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0006858	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0002650	OMIM:616688	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003487	PMID:7964809	PCS		3/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001288	PMID:7964809	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001761	PMID:7964809	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0006937	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001263	OMIM:616688	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0001284	PMID:7964809	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0007078	PMID:7964809	PCS		4/4			P	HPO:probinson[2022-07-17];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0007256	OMIM:616688	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003438	PMID:7964809	PCS		1/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0006886	PMID:7964809	PCS		2/4			P	HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0000006	PMID:7964809	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-17]
OMIM:616688	Charcot-Marie-Tooth disease, axonal, type 2Z		HP:0003677	OMIM:616688	TAS					C	HPO:skoehler[2017-07-13]
OMIM:617596	Maleylacetoacetate isomerase deficiency		HP:0001410	PMID:27876694	PCS		0/3			P	HPO:probinson[2020-08-02];HPO:probinson[2024-03-15]
OMIM:617596	Maleylacetoacetate isomerase deficiency		HP:0000007	PMID:27876694	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:607785	Juvenile myelomonocytic leukemia		HP:0001442	OMIM:607785	TAS					I	HPO:probinson[2013-01-09]
OMIM:607785	Juvenile myelomonocytic leukemia		HP:0012209	PMID:25939664	PCS	HP:0003593				P	HPO:probinson[2013-03-12];HPO:probinson[2022-03-26]
OMIM:607785	Juvenile myelomonocytic leukemia		HP:0000006	PMID:25939664	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000024	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000365	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0004322	PMID:7189577	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0002383	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0011839	PMID:22351933	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0003095	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0003729	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0002718	OMIM:307200	TAS					P	HPO:probinson[2012-07-19]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000999	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0001287	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0002014	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000010	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0002750	PMID:7189577	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000031	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0002090	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0001419	PMID:7189577	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000509	PMID:22351933	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0030252	PMID:22351933	PCS		3/4			P	HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000403	PMID:22351933	IEA		2/4			P	HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000824	PMID:22351933	PCS		2/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000823	PMID:7189577	PCS		2/2			P	HPO:probinson[2021-07-15]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0000246	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0001412	OMIM:307200	IEA					P	HPO:iea[2009-02-17]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0002743	OMIM:307200	TAS					P	HPO:probinson[2012-07-19]
OMIM:307200	Isolated growth hormone deficiency, type III, with agammaglobulinemia		HP:0003139	PMID:22351933	PCS		3/4			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-15]
OMIM:142900	Holt-Oram syndrome		HP:0011939	PMID:10842287	PCS		1/3			P	HPO:probinson[2024-07-22]
OMIM:142900	Holt-Oram syndrome		HP:0000882	PMID:17534187;PMID:12789647	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0005773	PMID:16917909	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0031546	PMID:10077612	PCS		14/36			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0010567	PMID:18706711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0009460	PMID:10842287	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000914	PMID:18706711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0009623	PMID:17534187;PMID:18351627	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000878	PMID:17534187;PMID:20519243	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009622	PMID:22190901	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0040019	OMIM:142900	PCS		33/55			P	HPO:iea[2018-03-13]
OMIM:142900	Holt-Oram syndrome		HP:0200021	PMID:20519243	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001688	PMID:22190901;PMID:25216260;PMID:29755943	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0004058	PMID:20519243	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0005301	PMID:10077612;PMID:34490705;PMID:20519243;PMID:36444245	PCS		4/39			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0003363	PMID:12789647	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011927	PMID:8730285;PMID:16917909	PCS		31/58			P	HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0010035	PMID:34490705;PMID:16917909;PMID:18351627	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0100379	PMID:18351627	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000767	PMID:22190901;PMID:24408148;PMID:18706711;PMID:8730285	PCS		24/61			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009577	PMID:18351627	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0004209	PMID:12789647;PMID:18351627	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0002943	OMIM:142900	IEA					P	HPO:iea[2009-02-17]
OMIM:142900	Holt-Oram syndrome		HP:0000006	PMID:12789647;PMID:8730285	PCS		20/20			I	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2009-02-17]
OMIM:142900	Holt-Oram syndrome		HP:0004602	PMID:12789647	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0003577	PMID:10077612;PMID:27652283;PMID:30538526;PMID:27552067;PMID:18706711;PMID:27026770;PMID:36444245;PMID:28434921;PMID:26219450;PMID:33866394	PCS		51/52			C	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0010704	PMID:12789647;PMID:34490705;PMID:27552067;PMID:33866394	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001674	PMID:17534187;PMID:34490705;PMID:25216260;PMID:15710732;PMID:30538526;PMID:24408148;PMID:20519243;PMID:27026770;PMID:33866394;PMID:18351627;PMID:22190901;PMID:12789647;PMID:12818525;PMID:18828908;PMID:26401820;PMID:29755943;PMID:26219450;PMID:28434921;PMID:16917909;PMID:10842287	PCS		9/103			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000343	PMID:18828908	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000185	PMID:26219450	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0004383	OMIM:142900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:142900	Holt-Oram syndrome		HP:0100398	PMID:18351627	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011636	PMID:16917909	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011995	PMID:18706711	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0001709	PMID:33866394	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0010034	PMID:18351627	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0031297	PMID:25216260;PMID:15710732;PMID:24408148;PMID:27026770;PMID:18351627;PMID:27652283;PMID:26401820;PMID:29755943;PMID:26219450;PMID:16917909;PMID:10842287;PMID:10077612;PMID:17534187;PMID:34490705;PMID:30538526;PMID:18706711;PMID:20519243;PMID:33866394;PMID:22190901;PMID:12789647;PMID:12818525;PMID:18828908;PMID:27552067;PMID:36444245;PMID:28434921	PCS		1/153			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0030241	PMID:12818525	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001704	PMID:16917909	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000218	PMID:18706711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0009829	OMIM:142900	IEA					P	HPO:iea[2009-02-17]
OMIM:142900	Holt-Oram syndrome		HP:0003982	PMID:20519243;PMID:8730285	PCS		5/56			P	HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001684	PMID:17534187;PMID:34490705;PMID:25216260;PMID:15710732;PMID:30538526;PMID:24408148;PMID:20519243;PMID:18706711;PMID:27026770;PMID:33866394;PMID:18351627;PMID:12789647;PMID:27652283;PMID:27552067;PMID:26401820;PMID:8730285;PMID:36444245;PMID:29755943;PMID:26219450;PMID:28434921;PMID:16917909	PCS		47/130			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001162	PMID:18706711	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0000470	PMID:18706711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0002092	PMID:12789647;PMID:34490705;PMID:25216260;PMID:30538526;PMID:18706711;PMID:28434921;PMID:33866394;PMID:16917909	PCS		8/16			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011623	PMID:17534187;PMID:34490705;PMID:25216260;PMID:30538526;PMID:20519243;PMID:27026770;PMID:33866394;PMID:18351627;PMID:12789647;PMID:12818525;PMID:18828908;PMID:29755943;PMID:28434921;PMID:16917909;PMID:10842287	PCS		14/80			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001719	PMID:12789647	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001159	PMID:8730285	PCS		7/55			P	HPO:iea[2018-03-13]
OMIM:142900	Holt-Oram syndrome		HP:0003974	PMID:17534187;PMID:34490705;PMID:25216260;PMID:15710732;PMID:20519243;PMID:27026770;PMID:33866394;PMID:12789647;PMID:27652283;PMID:8730285;PMID:36444245;PMID:28434921;PMID:26219450;PMID:16917909	PCS		28/123			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000347	PMID:18828908;PMID:26219450	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001377	PMID:8730285;PMID:33866394	PCS		30/56			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2018-03-13]
OMIM:142900	Holt-Oram syndrome		HP:0004762	PMID:20519243	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0003031	PMID:10842287	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0010487	PMID:12789647	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0006394	PMID:16917909	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000954	PMID:22190901	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0006156	PMID:12789647	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009944	OMIM:142900	IEA					P	HPO:iea[2009-02-17]
OMIM:142900	Holt-Oram syndrome		HP:0001643	PMID:22190901;PMID:10077612;PMID:34490705;PMID:25216260;PMID:27552067;PMID:8730285;PMID:16917909	PCS		9/53			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001642	PMID:17534187	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0004756	PMID:20519243	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0002974	PMID:12789647	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009824	PMID:18706711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0003042	PMID:24408148	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011567	PMID:22190901	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011565	PMID:25216260;PMID:15710732;PMID:24408148;PMID:27026770;PMID:18351627;PMID:27652283;PMID:26401820;PMID:29755943;PMID:26219450;PMID:16917909;PMID:10842287;PMID:17534187;PMID:10077612;PMID:34490705;PMID:30538526;PMID:18706711;PMID:20519243;PMID:33866394;PMID:22190901;PMID:12789647;PMID:12818525;PMID:18828908;PMID:27552067;PMID:36444245;PMID:28434921	PCS		1/153			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0005180	PMID:34490705;PMID:27652283;PMID:26219450	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0034198	PMID:27026770	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0009777	PMID:17534187;PMID:10077612;PMID:34490705;PMID:25216260;PMID:15710732;PMID:30538526;PMID:24408148;PMID:20519243;PMID:18706711;PMID:27026770;PMID:33866394;PMID:18351627;PMID:12789647;PMID:12818525;PMID:27652283;PMID:26401820;PMID:8730285;PMID:36444245;PMID:29755943;PMID:28434921;PMID:26219450;PMID:16917909;PMID:10842287	PCS		59/186			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009535	PMID:12789647	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009812	PMID:10077612;PMID:17534187;PMID:15710732;PMID:34490705;PMID:25216260;PMID:30538526;PMID:24408148;PMID:20519243;PMID:18706711;PMID:27026770;PMID:33866394;PMID:18351627;PMID:22190901;PMID:12789647;PMID:12818525;PMID:27652283;PMID:18828908;PMID:27552067;PMID:26401820;PMID:29755943;PMID:28434921;PMID:26219450;PMID:10842287;PMID:16917909	PCS		1/151			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0002986	PMID:10842287	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001653	PMID:17534187;PMID:16917909	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000960	PMID:22190901	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009778	PMID:17534187;PMID:10077612;PMID:34490705;PMID:25216260;PMID:15710732;PMID:30538526;PMID:24408148;PMID:20519243;PMID:18706711;PMID:27026770;PMID:33866394;PMID:18351627;PMID:12789647;PMID:12818525;PMID:27652283;PMID:26401820;PMID:29755943;PMID:26219450;PMID:28434921;PMID:16917909;PMID:10842287	PCS		32/98			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0003834	PMID:33866394	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0002984	OMIM:142900;PMID:17534187;PMID:10077612;PMID:34490705;PMID:30538526;PMID:18706711;PMID:27026770;PMID:33866394;PMID:12789647;PMID:12818525;PMID:27552067;PMID:26219450;PMID:16917909	PCS		64/144			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001655	PMID:17534187;PMID:34490705;PMID:25216260;PMID:15710732;PMID:24408148;PMID:20519243;PMID:27026770;PMID:33866394;PMID:18351627;PMID:22190901;PMID:12789647;PMID:12818525;PMID:27652283;PMID:18828908;PMID:26401820;PMID:29755943;PMID:26219450;PMID:28434921;PMID:16917909;PMID:10842287	PCS		4/103			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009813	PMID:17534187;PMID:10077612;PMID:34490705;PMID:15710732;PMID:25216260;PMID:30538526;PMID:24408148;PMID:20519243;PMID:18706711;PMID:27026770;PMID:33866394;PMID:18351627;PMID:22190901;PMID:12789647;PMID:12818525;PMID:27652283;PMID:18828908;PMID:27552067;PMID:26401820;PMID:29755943;PMID:28434921;PMID:26219450;PMID:10842287;PMID:16917909	PCS		10/153			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001199	PMID:17534187;PMID:10077612;PMID:34490705;PMID:25216260;PMID:15710732;PMID:24408148;PMID:20519243;PMID:18706711;PMID:27026770;PMID:33866394;PMID:18351627;PMID:22190901;PMID:12789647;PMID:12818525;PMID:27652283;PMID:27552067;PMID:26401820;PMID:8730285;PMID:29755943;PMID:28434921;PMID:26219450;PMID:16917909;PMID:10842287	PCS		46/186			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001233	PMID:33866394	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0004220	PMID:17534187;PMID:18351627	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0005792	PMID:17534187;PMID:12789647;PMID:34490705;PMID:15710732;PMID:27652283;PMID:30538526;PMID:27552067;PMID:18706711;PMID:8730285;PMID:33866394;PMID:16917909	PCS		40/85			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001191	OMIM:142900;PMID:10077612;PMID:27026770	PCS		40/42			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2009-02-17]
OMIM:142900	Holt-Oram syndrome		HP:0030718	PMID:18706711	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0001629	PMID:17534187;PMID:10077612;PMID:34490705;PMID:15710732;PMID:24408148;PMID:20519243;PMID:18706711;PMID:27026770;PMID:22190901;PMID:12789647;PMID:27652283;PMID:27552067;PMID:26401820;PMID:8730285;PMID:36444245;PMID:26219450;PMID:16917909	PCS		56/125			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011682	PMID:17534187;PMID:34490705;PMID:25216260;PMID:30538526;PMID:20519243;PMID:27026770;PMID:33866394;PMID:18351627;PMID:12789647;PMID:12818525;PMID:18828908;PMID:29755943;PMID:28434921;PMID:16917909;PMID:10842287	PCS		9/80			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009486	PMID:26219450	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-20]
OMIM:142900	Holt-Oram syndrome		HP:0000774	PMID:12789647	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0000894	PMID:18828908;PMID:8730285	PCS		41/56			P	HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011709	PMID:16917909	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001245	OMIM:142900	PCS		42/55			P	HPO:iea[2018-03-13]
OMIM:142900	Holt-Oram syndrome		HP:0003022	PMID:12789647;PMID:34490705;PMID:30538526;PMID:8730285;PMID:33866394	PCS		25/82			P	ORCID:0000-0002-0736-9199[2024-07-20];HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011705	PMID:22190901;PMID:16917909	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0031134	PMID:34490705	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0011664	PMID:34490705;PMID:26401820;PMID:29755943;PMID:10842287	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0009751	PMID:8730285	PCS		34/55			P	HPO:iea[2009-02-17]
OMIM:142900	Holt-Oram syndrome		HP:0000268	PMID:22190901	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001631	PMID:17534187;PMID:10077612;PMID:12789647;PMID:25216260;PMID:12818525;PMID:18828908;PMID:20519243;PMID:29755943;PMID:33866394;PMID:16917909;PMID:10842287	PCS		50/52			P	ORCID:0000-0002-0736-9199[2024-07-20];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:142900	Holt-Oram syndrome		HP:0001634	PMID:16917909;PMID:18351627	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:135550	Fibromatosis, gingival, with progressive deafness		HP:0000408	OMIM:135550	IEA					P	HPO:iea[2009-02-17]
OMIM:135550	Fibromatosis, gingival, with progressive deafness		HP:0000169	OMIM:135550	IEA					P	HPO:iea[2009-02-17]
OMIM:135550	Fibromatosis, gingival, with progressive deafness		HP:0000006	OMIM:135550	IEA					I	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0003577	PMID:30642278	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:302350	Nance-Horan syndrome		HP:0000482	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0040080	PMID:30642278	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:302350	Nance-Horan syndrome		HP:0008031	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0000639	PMID:30642278	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0000717	OMIM:302350;PMID:30642278	PCS		10/12			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:302350	Nance-Horan syndrome		HP:0000519	OMIM:302350	TAS			MALE		P	HPO:skoehler[2013-01-22]
OMIM:302350	Nance-Horan syndrome		HP:0006332	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0001500	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0001423	OMIM:302350	IEA					I	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0000699	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0009803	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0000275	PMID:30642278	PCS		2/2			P	HPO:probinson[2012-05-01]
OMIM:302350	Nance-Horan syndrome		HP:0000572	OMIM:302350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:302350	Nance-Horan syndrome		HP:0000276	OMIM:302350	TAS					P	HPO:probinson[2012-05-01]
OMIM:302350	Nance-Horan syndrome		HP:0100018	PMID:30642278	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:302350	Nance-Horan syndrome		HP:0000426	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0000448	PMID:30642278	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0000689	PMID:30642278	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:302350	Nance-Horan syndrome		HP:0000568	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0000400	OMIM:302350	TAS					P	HPO:probinson[2009-02-17]
OMIM:302350	Nance-Horan syndrome		HP:0006346	PMID:29042737;PMID:30642278	PCS		3/3			P	HPO:iea[2009-02-17];HP:probinson[2019-01-23];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:302350	Nance-Horan syndrome		HP:0011092	PMID:29042737;PMID:30642278	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-28];HP:probinson[2019-01-23]
OMIM:302350	Nance-Horan syndrome		HP:0000501	OMIM:302350	IEA					P	HPO:iea[2009-02-17]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0002059	PMID:31944455	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0031936	PMID:31944455	PCS					P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0001250	PMID:31944455	PCS		2/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0001263	PMID:31944455	PCS	HP:0003593	2/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0002151	PMID:31944455	PCS		2/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0001350	PMID:31944455	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0001290	PMID:31944455	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0100660	PMID:31944455	PCS	HP:0011463	2/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0012751	PMID:31944455	PCS					P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0000639	PMID:31944455	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0001639	PMID:31944455	PCS	HP:0003621	1/3			P	HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0000007	PMID:31944455	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618855	Combined oxidative phosphorylation deficiency 44		HP:0002600	PMID:31944455	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:619593	Cataract 49		HP:0003621	PMID:30585370	PCS		3/7			C	HPO:probinson[2021-10-31];HPO:probinson[2021-10-31]
OMIM:619593	Cataract 49		HP:0010924	PMID:30585370	PCS		7/7			P	HPO:probinson[2021-10-31]
OMIM:619593	Cataract 49		HP:0000639	PMID:30585370	PCS		4/6			P	HPO:probinson[2021-10-31]
OMIM:619593	Cataract 49		HP:0011463	PMID:30585370	PCS		4/7			C	HPO:probinson[2021-10-31];HPO:probinson[2021-10-31]
OMIM:619593	Cataract 49		HP:0007663	PMID:30585370	PCS		6/6			P	HPO:probinson[2021-10-31]
OMIM:619593	Cataract 49		HP:0000006	PMID:30585370	TAS					I	HPO:probinson[2021-10-31];HPO:probinson[2021-10-31]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0008209	PMID:12707859	PCS		2/2			P	HPO:probinson[2023-06-27];HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0002354	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0000518	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0001260	PMID:12707859	PCS		1/2			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0000869	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0007340	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0002352	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0000007	PMID:11704758	PCS					I	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0002317	PMID:12707859	PCS	HP:0003621	1/2			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0002317	PMID:21484434	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0000648	PMID:12707859	PCS		0/2			P	HPO:probinson[2023-06-27]
OMIM:620312	Leukoencephalopathy with vanishing white matter 2, with or without ovarian failure		HP:0001257	PMID:12707859	PCS		2/2			P	HPO:probinson[2023-06-27]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0003236	PMID:26805782;PMID:26805781	PCS		14/14			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001695	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001332	OMIM:616878	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:6000476	PMID:26805782;PMID:26805781	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001250	PMID:26805781	PCS		9/12			P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002066	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001251	PMID:26805782;PMID:26805781	PCS		2/2			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0003593	PMID:26805782;PMID:26805781	PCS		5/15			C	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001290	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002061	PMID:26805782	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002180	OMIM:616878	TAS				HP:0003676	P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0012544	PMID:26805781	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0011463	PMID:26805782;PMID:26805781	PCS		8/15			C	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001324	PMID:26805781	PCS					P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001249	PMID:26805782;PMID:26805781	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-21];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0004756	PMID:26805782;PMID:26805781	PCS		4/12			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002311	PMID:26805781	PCS					P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0031956	PMID:26805782;PMID:26805781	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0000252	PMID:26805782;PMID:26805781	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-21];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001264	OMIM:616878	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002510	OMIM:616878	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001344	PMID:26805782	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001663	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0003487	PMID:26805781	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001662	PMID:26805781	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0003201	PMID:26805782;PMID:26805781	PCS		13/15			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001260	PMID:26805782;PMID:26805781	PCS		2/2			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001263	PMID:26805782;PMID:26805781	PCS		14/14			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002151	PMID:26805781	PCS		9/11			P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0045045	PMID:26805782	PCS					P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0005184	PMID:26805782;PMID:26805781	PCS		8/13			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0012411	OMIM:616878	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0010314	OMIM:616878	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0000407	OMIM:616878;PMID:26805782	PCS		3/11			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0000007	PMID:26805781	PCS					I	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0000648	OMIM:616878	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002307	PMID:26805781	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001259	PMID:26805782	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0006801	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002169	PMID:26805781	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001270	PMID:26805782	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0031964	PMID:26805782;PMID:26805781	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002919	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002913	PMID:26805782;PMID:26805781	PCS		2/2			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001987	PMID:26805781	PCS		9/11			P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001943	PMID:26805782;PMID:26805781	PCS		11/14			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001664	PMID:26805782;PMID:26805781	PCS		3/13			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001348	PMID:26805781	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001942	PMID:26805781	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0003128	PMID:26805782;PMID:26805781	PCS		12/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-21];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002058	PMID:26805781	PCS		4/4			P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002059	PMID:26805782;PMID:26805781	PCS		4/11			P	HPO:probinson[2017-06-20];ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0003621	PMID:26805781	PCS		2/12			C	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002133	PMID:26805782	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0002376	PMID:26805781	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001288	PMID:26805781	PCS					P	HPO:probinson[2017-06-20]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0001639	OMIM:616878	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0006682	PMID:26805781	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0200136	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0000821	OMIM:616878	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616878	Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration		HP:0008942	PMID:26805781	PCS					P	HPO:probinson[2017-06-20]
OMIM:210740	Bangstad syndrome		HP:0000275	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0003510	OMIM:210740	IEA					P	HPO:skoehler[2015-01-27]
OMIM:210740	Bangstad syndrome		HP:0002073	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0001090	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0008193	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0001518	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0000007	OMIM:210740	IEA					I	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0006872	OMIM:210740;PMID:2662702	PCS		20/20			P	HP:probinson[2019-02-18];HPO:probinson[2013-03-31]
OMIM:210740	Bangstad syndrome		HP:0000444	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0000278	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0000831	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0000853	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0001249	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:210740	Bangstad syndrome		HP:0001876	OMIM:210740	IEA					P	HPO:iea[2009-02-17]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0002015	PMID:35484142	PCS		9/9			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0003621	PMID:35484142	PCS		2/7			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0011968	PMID:35484142	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0003593	PMID:35484142	PCS		1/7			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0003690	PMID:35484142	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0001270	PMID:35484142	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0002093	PMID:35484142	PCS		9/9			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0034677	PMID:35484142	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0001618	PMID:35484142	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0011463	PMID:35484142	PCS		2/7			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0011462	PMID:35484142	PCS		2/7			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0000508	PMID:35484142	PCS		11/11			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0000602	PMID:35484142	PCS		11/11			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0002505	PMID:35484142	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0003701	PMID:35484142	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0003327	PMID:35484142	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0001324	PMID:35484142	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0000006	PMID:35484142	PCS					I	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620460	Oculopharyngeal muscular dystrophy 2		HP:0025406	PMID:35484142	PCS		7/7			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0000054	PMID:31883645	PCS		3/3	MALE		P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0003164	PMID:31883645	PCS		4/4			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0000458	PMID:31883645	PCS		4/4			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0040171	PMID:31883645	PCS		3/3	MALE		P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0008214	PMID:31883645	PCS		1/1	FEMALE		P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0000006	PMID:31883645	PCS					I	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0000028	PMID:31883645	PCS		3/3	MALE		P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0000786	PMID:31883645	PCS		1/1	FEMALE		P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618841	Hypogonadotropic hypogonadism 25 with anosmia		HP:0008724	PMID:31883645	PCS		1/1			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0031627	PMID:36443312	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0003596	PMID:36443312	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0001250	PMID:36443312	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0003165	PMID:36443312	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0001260	PMID:36443312	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0003493	PMID:36443312	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0004363	PMID:36443312	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0001251	PMID:36443312	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0012229	PMID:36443312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0025041	PMID:36443312	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0100543	PMID:36443312	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0007352	PMID:36443312	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0011462	PMID:36443312	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0000007	PMID:36443312	PCS					I	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0100529	PMID:36443312	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0002315	PMID:36443312	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0002401	PMID:36443312	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:621018	Basal ganglia calcification, idiopathic, 10, autosomal recessive		HP:0007229	PMID:36443312	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0002257	PMID:31630787	PCS		6/6			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0002783	PMID:31630787	PCS		6/6			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0003363	PMID:31630787	PCS		3/6			P	HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0002110	PMID:31630787	PCS		6/6			P	HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0031245	PMID:31630787	PCS		6/6			P	HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0002788	PMID:31630787	PCS		6/6			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0011109	PMID:31630787	PCS		6/6			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0000006	PMID:31630787	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0010953	PMID:31630787	PCS	HP:0003623	6/6			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618699	Ciliary dyskinesia, primary, 43		HP:0002643	PMID:31630787	PCS		4/6			P	HPO:probinson[2020-07-23]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0001254	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002089	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002384	PMID:35913762	PCS	HP:0003593	2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0001272	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0001250	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0030674	PMID:36562171	PCS		1/1			C	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0003097	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0003593	PMID:35913762	PCS		2/2			C	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002280	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0100704	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002119	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0005968	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0001347	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0008936	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0032989	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002059	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0010836	PMID:35913762	PCS		0/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0001762	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0000474	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0001640	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002098	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002151	PMID:35913762	PCS		2/2		HP:0012825	P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002490	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0034823	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-07-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0005180	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0032988	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0000807	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0033144	PMID:35913762	PCS		0/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002509	PMID:35913762	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0000007	PMID:35913762	PCS					I	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0005736	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620306	Neurodegeneration and seizures due to copper transport defect		HP:0002107	PMID:36562171	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001397	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002487	OMIM:615356	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002465	OMIM:615356	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0003236	PMID:23830518	PCS		8/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002540	OMIM:615356	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0000486	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001332	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0004322	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001272	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001250	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001252	PMID:23830518	PCS		1/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0003394	PMID:23830518	PCS		2/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001251	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002240	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001290	OMIM:615356	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0003391	OMIM:615356	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0000518	PMID:23830518	PCS		1/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0011463	PMID:23830518	PCS		3/3			C	HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0003307	OMIM:615356	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002515	OMIM:615356	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0003429	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0003701	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002910	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001249	PMID:23830518	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0003326	PMID:23830518	PCS		3/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002059	PMID:23830518	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001385	PMID:23830518	PCS		3/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0000252	PMID:23830518	PCS		4/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002353	OMIM:615356	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002650	PMID:23830518	PCS		3/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002078	PMID:23830518	PCS		5/8			P	HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001288	OMIM:615356	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002571	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0011968	OMIM:615356	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001260	OMIM:615356	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001263	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002072	PMID:23830518	PCS		5/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0100633	OMIM:615356	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0011098	OMIM:615356	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0000007	PMID:23830518	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0006785	PMID:23830518	PCS		8/8			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001511	OMIM:615356	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0002305	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0000545	PMID:23830518	PCS		2/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-04]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0001337	OMIM:615356	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615356	Muscular dystrophy, limb-girdle, autosomal recessive 18		HP:0000522	OMIM:615356	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0002024	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0004322	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0002783	PMID:27913302	PCS	HP:0003593	1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000460	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0002240	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0012302	PMID:27913302	PCS	HP:0011462	1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0040154	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0100806	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0001943	PMID:27913302	PCS	HP:0003623	1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000218	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0006579	PMID:27913302	PCS	HP:0003623	1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0003623	PMID:27913302	PCS		1/1			C	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000275	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0004313	PMID:27913302	PCS		0/1			P	HPO:probinson[2013-12-14];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000431	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0410300	PMID:27913302	PCS		1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0030388	PMID:27913302	PCS		1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0001581	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0011107	PMID:27913302	PCS		1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0012089	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0009890	PMID:27913302	PCS		1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000007	PMID:27913302	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000768	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0002788	PMID:27913302	PCS	HP:0003593	1/1			P	HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000300	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0000347	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0001238	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0002721	PMID:27913302	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-01-30]
OMIM:233600	Immunodeficiency 59 and hypoglycemia		HP:0002028	PMID:27913302	PCS		1/1			P	HPO:probinson[2022-01-30]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000582	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0002188	PMID:31201375	PCS		1/12			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000486	PMID:31201375	PCS		4/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000463	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000540	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0002162	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0001252	PMID:31201375	PCS		10/16			P	HPO:probinson[2022-06-03]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0003593	PMID:31201375	PCS					C	HPO:probinson[2022-06-03]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0010862	PMID:31201375	PCS					P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0002280	PMID:31201375	PCS		1/12			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000639	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0011220	PMID:31201375	PCS		5/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000316	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0008872	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0002714	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0001763	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000457	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0001249	PMID:31201375	PCS					P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0001385	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0031936	PMID:31201375	PCS		12/15			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0002079	PMID:31201375	PCS		2/12			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000490	PMID:31201375	PCS		4/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0001263	PMID:31201375	PCS					P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000272	PMID:31201375	PCS		4/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0002194	PMID:31201375	PCS					P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0001182	PMID:31201375	PCS		3/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0007074	PMID:31201375	PCS		1/12			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000407	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000729	PMID:31201375	PCS		7/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000601	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000648	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0004209	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000405	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000268	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0001357	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0200055	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000322	PMID:31201375	PCS		4/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000006	PMID:31201375	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000248	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000369	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000303	PMID:31201375	PCS		2/16			P	HPO:probinson[2020-07-23]
OMIM:618672	Intellectual developmental disorder with speech delay, autism, and dysmorphic facies		HP:0000269	PMID:31201375	PCS		1/16			P	HPO:probinson[2020-07-23]
OMIM:616887	Intellectual developmental disorder, autosomal recessive 52		HP:0001250	PMID:26566883	PCS	HP:0003593				P	HPO:probinson[2017-06-26]
OMIM:616887	Intellectual developmental disorder, autosomal recessive 52		HP:0001263	PMID:26566883	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-05]
OMIM:616887	Intellectual developmental disorder, autosomal recessive 52		HP:0000718	PMID:26566883	PCS		1/7			P	HPO:probinson[2022-09-05]
OMIM:616887	Intellectual developmental disorder, autosomal recessive 52		HP:0003593	PMID:26566883	PCS		14/14			C	HPO:probinson[2022-09-05];HPO:skoehler[2017-07-13];HPO:probinson[2022-09-05]
OMIM:616887	Intellectual developmental disorder, autosomal recessive 52		HP:0000007	PMID:26566883	PCS					I	HPO:probinson[2017-06-26]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0002069	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0008936	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0000252	OMIM:616139	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0002521	PMID:24272827	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001344	PMID:24272827	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001332	PMID:24272827	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001250	OMIM:616139	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0011968	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001252	PMID:24272827	PCS		1/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001263	PMID:24272827	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-18]
OMIM:616139	Epileptic encephalopathy, early infantile, 27		HP:0003593	PMID:24272827	PCS		2/2			C	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0032794	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0002072	OMIM:616139	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0040196	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0100660	OMIM:616139	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0012469	PMID:24272827	PCS		2/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0011097	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0000817	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0200134	PMID:24272827	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0025336	PMID:24272827	PCS		2/2			P	HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001257	OMIM:616139	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001249	OMIM:616139	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0000006	PMID:24272827	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-18]
OMIM:616139	Developmental and epileptic encephalopathy 27		HP:0001336	PMID:24272827	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:618114	Liddle syndrome 2		HP:0003621	PMID:7550319;PMID:17634077	PCS		3/7			C	HPO:probinson[2022-06-13];HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:618114	Liddle syndrome 2		HP:0011462	PMID:7550319	PCS		4/6			C	HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:618114	Liddle syndrome 2		HP:0003351	PMID:7550319;PMID:17634077	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:618114	Liddle syndrome 2		HP:0000822	PMID:7550319;PMID:17634077	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:618114	Liddle syndrome 2		HP:0200114	PMID:17634077	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-13]
OMIM:618114	Liddle syndrome 2		HP:0002900	PMID:7550319;PMID:17634077	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:618114	Liddle syndrome 2		HP:0004319	PMID:7550319;PMID:17634077	PCS		2/7			P	HPO:probinson[2022-06-13]
OMIM:618114	Liddle syndrome 2		HP:0000006	PMID:7550319	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-13]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001254	PMID:8486760	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001297	OMIM:237300	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0002013	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0005961	OMIM:237300	PCS					P	HPO:iea[2010-12-08]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001250	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0003572	OMIM:237300	PCS					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001263	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001251	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0002181	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001508	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0000737	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0000007	PMID:8486760	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001987	PMID:8486760	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001951	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001950	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001249	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0002038	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0001259	OMIM:237300	IEA					P	HPO:iea[2009-02-17]
OMIM:237300	Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to		HP:0003623	PMID:8486760	PCS		1/1			C	HPO:probinson[2022-05-30]
OMIM:613055	Atrial fibrillation 8, susceptibility to		HP:0003581	PMID:37449401	PCS					C	HPO:probinson[2024-03-12]
OMIM:613055	Atrial fibrillation 8, susceptibility to		HP:0005110	PMID:37449401	PCS					P	HPO:probinson[2024-03-12]
OMIM:613055	Atrial fibrillation 8, susceptibility to		HP:0000006	PMID:37449401	PCS					I	HPO:probinson[2024-03-12]
OMIM:180300	Rheumatoid arthritis		HP:0001386	PMID:27156434	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0003565	PMID:27156434	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0005764	PMID:28723028	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0001387	PMID:27156434	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0001370	PMID:28723028	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0012378	PMID:9652497	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0011227	PMID:27156434	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0012276	PMID:28723028	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0006150	PMID:28723028	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0002829	PMID:27156434	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0033034	PMID:28723028	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0006252	PMID:28723028	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0001945	PMID:9652497	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0001824	PMID:9652497	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0002923	PMID:28723028	PCS					P	HPO:probinson[2020-09-30]
OMIM:180300	Rheumatoid arthritis		HP:0002633	PMID:28723028	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-09-30]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0002058	PMID:23489661	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0003324	OMIM:605637	TAS					P	HPO:skoehler[2015-04-05]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0002015	PMID:23489661	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0003577	PMID:23489661	PCS		1/1			C	HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0002650	PMID:23489661	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0003198	PMID:23489661	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0003691	OMIM:605637	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0002460	OMIM:605637	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0001290	PMID:23489661	PCS	HP:0003577	1/1			P	HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0100299	OMIM:605637	IEA					P	HPO:skoehler[2013-01-09]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0000508	PMID:23489661	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0002803	OMIM:605637	IEA					P	HPO:skoehler[2015-12-30]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0000602	PMID:23489661	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0000007	OMIM:605637	IEA					I	HPO:skoehler[2013-01-09]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0002515	PMID:23489661	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0000218	PMID:23489661	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0003803	PMID:23489661	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0003701	OMIM:605637	TAS					P	HPO:skoehler[2015-04-05]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0000006	PMID:11114175	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-31]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0000467	OMIM:605637	TAS					P	HPO:skoehler[2015-04-05]
OMIM:605637	Myopathy, proximal, and ophthalmoplegia		HP:0003557	PMID:23489661	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:104000	Alopecia areata 1		HP:0002960	OMIM:104000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:104000	Alopecia areata 1		HP:0002289	OMIM:104000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:104000	Alopecia areata 1		HP:0007418	OMIM:104000	IEA					P	HPO:iea[2009-02-17]
OMIM:104000	Alopecia areata 1		HP:0002232	OMIM:104000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:104000	Alopecia areata 1		HP:0001426	OMIM:104000	IEA					I	HPO:iea[2009-02-17]
OMIM:104000	Alopecia areata 1		HP:0001803	OMIM:104000	IEA					P	HPO:iea[2009-02-17]
OMIM:104000	Alopecia areata 1		HP:0030804	OMIM:104000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0003236	PMID:20116073	PCS		5/5			P	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3		HP:0003687	PMID:20116073	PCS					P	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0003596	PMID:20116073	PCS		3/5			C	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0003198	PMID:20116073	PCS					P	HPO:skoehler[2015-08-29];HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0003155	PMID:20116073	PCS		3/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0100299	PMID:20116073	PCS		2/3			P	HPO:skoehler[2015-08-29];HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3		HP:0100297	PMID:20116073	PCS					P	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3		HP:0009023	PMID:20116073	PCS		5/5			P	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0011462	PMID:20116073	PCS		2/5			C	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0009027	PMID:20116073	PCS		5/5			P	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0003738	PMID:20116073	PCS		2/5			P	HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0003805	PMID:20116073	PCS		2/3			P	HPO:skoehler[2015-08-29];HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0006785	PMID:20116073	PCS					P	HPO:skoehler[2015-08-29];HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0002505	PMID:20116073	PCS	HP:0003596	3/5			P	HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3		HP:0000006	PMID:20116073	PCS					I	HPO:skoehler[2015-08-29];HPO:probinson[2022-04-11]
OMIM:615424	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3		HP:0003557	PMID:20116073	PCS					P	HPO:probinson[2022-04-11]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0000709	OMIM:277730	TAS					P	HPO:skoehler[2010-06-20]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0001289	OMIM:277730	IEA					P	HPO:iea[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0002354	OMIM:277730	TAS					P	HPO:skoehler[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0001271	OMIM:277730	IEA					P	HPO:iea[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0000508	OMIM:277730	IEA					P	HPO:iea[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0001251	OMIM:277730	IEA					P	HPO:iea[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0000602	OMIM:277730	IEA					P	HPO:iea[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0000007	OMIM:277730	IEA					I	HPO:iea[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0031258	OMIM:277730	IEA					P	HPO:skoehler[2018-10-08]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0000666	OMIM:277730	IEA					P	HPO:iea[2009-02-17]
OMIM:277730	Wernicke-Korsakoff syndrome		HP:0001259	OMIM:277730	TAS					P	HPO:skoehler[2009-02-17]
OMIM:149100	Knuckle pads		HP:0000924	OMIM:149100	IEA					P	HPO:iea[2009-02-17]
OMIM:149100	Knuckle pads		HP:0001482	OMIM:149100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:149100	Knuckle pads		HP:0000006	OMIM:149100	IEA					I	HPO:iea[2009-02-17]
OMIM:618666	Sitosterolemia 2		HP:0003124	PMID:11099417;PMID:20719861	PCS		11/11			P	HPO:probinson[2020-11-30]
OMIM:618666	Sitosterolemia 2		HP:0033341	PMID:11099417	PCS					P	HPO:probinson[2020-12-07]
OMIM:618666	Sitosterolemia 2		HP:0010874	PMID:11099417;PMID:20719861	PCS		11/11			P	HPO:probinson[2020-11-30]
OMIM:618666	Sitosterolemia 2		HP:0000007	PMID:11138003	PCS					I	HPO:probinson[2020-11-30];HPO:probinson[2020-11-30]
OMIM:618666	Sitosterolemia 2		HP:0005181	PMID:11099417	PCS					P	HPO:probinson[2020-11-30]
OMIM:616893	Nephrotic syndrome, type 13		HP:0003774	PMID:26878725	PCS					P	HPO:probinson[2017-06-23]
OMIM:616893	Nephrotic syndrome, type 13		HP:0000097	PMID:26878725	PCS					P	HPO:probinson[2017-06-23]
OMIM:616893	Nephrotic syndrome, type 13		HP:0000007	PMID:26878725	PCS					I	HPO:probinson[2017-06-23]
OMIM:616893	Nephrotic syndrome, type 13		HP:0012588	PMID:26878725	PCS					P	HPO:probinson[2017-06-23]
OMIM:615342	Pulmonary hypertension, primary, 2		HP:0003676	OMIM:615342	TAS					C	HPO:skoehler[2013-10-06]
OMIM:615342	Pulmonary hypertension, primary, 2		HP:0003621	PMID:19211612	PCS		1/1			C	HPO:probinson[2022-09-06]
OMIM:615342	Pulmonary hypertension, primary, 2		HP:0003829	PMID:19211612	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-06]
OMIM:615342	Pulmonary hypertension, primary, 2		HP:0002092	PMID:19211612	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-06]
OMIM:615342	Pulmonary hypertension, primary, 2		HP:0031687	PMID:19211612	PCS		1/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:615342	Pulmonary hypertension, primary, 2		HP:0005317	PMID:19211612	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-06]
OMIM:615342	Pulmonary hypertension, primary, 2		HP:0000006	PMID:19211612	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-06]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0000023	OMIM:600001	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0004388	OMIM:600001	TAS	HP:0030674	HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001250	OMIM:600001	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001195	PMID:24385578	PCS		1/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0003076	OMIM:600001	IEA					P	HPO:iea[2009-02-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0011611	PMID:22158542	PCS	HP:0030674	1/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0003074	OMIM:600001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0031369	PMID:22158542	PCS		1/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0000819	OMIM:600001	IEA					P	HPO:iea[2009-02-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0011581	PMID:22158542	PCS	HP:0030674	1/15			P	HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001508	OMIM:600001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001629	PMID:22158542	PCS		5/15			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0011682	PMID:22158542	PCS		1/15			P	HPO:skoehler[2013-05-31];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001669	OMIM:600001	IEA					P	HPO:iea[2009-02-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001643	OMIM:600001	IEA					P	HPO:iea[2009-02-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001643	PMID:24385578	PCS	HP:0003577	1/4			P	HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001642	OMIM:600001	IEA					P	HPO:iea[2009-02-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0000776	PMID:24385578	PCS	HP:0003577	3/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0004415	PMID:22158542	PCS	HP:0003577	3/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0000891	PMID:24385578	PCS	HP:0003577	1/4			P	HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0000252	OMIM:600001	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001660	PMID:22158542	PCS		1/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0011629	PMID:24385578	IEA	HP:0003577	1/4			P	HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0000073	PMID:24385578	PCS	HP:0003577	1/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0002594	OMIM:600001	IEA					P	HPO:iea[2009-02-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001263	PMID:22158542	PCS		7/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0011467	PMID:22158542	PCS		4/15			P	HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0011573	OMIM:600001	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0009112	PMID:22158542	PCS	HP:0030674	2/15			P	HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001636	PMID:22158542	PCS		3/15			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001636	PMID:24385578	PCS	HP:0003577	1/4			P	HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001537	PMID:22158542	PCS		1/15			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001511	OMIM:600001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001631	PMID:22158542	PCS	HP:0030674	6/15			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0005912	PMID:22158542	PCS		1/15			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0000006	PMID:22158542	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0002566	PMID:22158542	PCS		1/15			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-12]
OMIM:600001	Pancreatic agenesis and congenital heart defects		HP:0001655	PMID:22158542	PCS	HP:0003623	2/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610212	Deafness, autosomal recessive 66		HP:0003577	PMID:25601850	PCS		8/8			C	HPO:probinson[2022-12-05]
OMIM:610212	Deafness, autosomal recessive 66		HP:0000407	PMID:25601850	PCS		8/8		HP:0012829	P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-05]
OMIM:610212	Deafness, autosomal recessive 66		HP:0000007	PMID:25601850	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-05]
OMIM:151001	Lentiginosis, inherited patterned		HP:0001034	OMIM:151001	IEA					P	HPO:iea[2009-02-17]
OMIM:151001	Lentiginosis, inherited patterned		HP:0000006	OMIM:151001	IEA					I	HPO:iea[2009-02-17]
OMIM:181750	Scleroderma, familial progressive		HP:0003761	OMIM:181750	IEA					P	HPO:iea[2009-02-17]
OMIM:181750	Scleroderma, familial progressive		HP:0100324	OMIM:181750	IEA					P	HPO:iea[2009-02-17]
OMIM:181750	Scleroderma, familial progressive		HP:0003220	OMIM:181750	IEA					P	HPO:iea[2009-02-17]
OMIM:181750	Scleroderma, familial progressive		HP:0011838	OMIM:181750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181750	Scleroderma, familial progressive		HP:0040012	OMIM:181750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:181750	Scleroderma, familial progressive		HP:0001009	OMIM:181750	IEA					P	HPO:iea[2009-02-17]
OMIM:181750	Scleroderma, familial progressive		HP:0001438	OMIM:181750	IEA					P	HPO:iea[2009-02-17]
OMIM:181750	Scleroderma, familial progressive		HP:0000006	OMIM:181750	TAS					I	HPO:skoehler[2013-05-29]
OMIM:172800	Piebald trait		HP:0001100	OMIM:172800	IEA					P	HPO:iea[2009-02-17]
OMIM:172800	Piebald trait		HP:0002664	OMIM:172800	IEA					P	HPO:iea[2009-02-17]
OMIM:172800	Piebald trait		HP:0002211	OMIM:172800	TAS					P	HPO:skoehler[2009-02-17]
OMIM:172800	Piebald trait		HP:0002251	OMIM:172800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:172800	Piebald trait		HP:0007443	OMIM:172800	TAS					P	HPO:probinson[2012-07-16]
OMIM:172800	Piebald trait		HP:0007542	OMIM:172800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:172800	Piebald trait		HP:0007544	OMIM:172800	TAS					P	HPO:probinson[2012-07-16]
OMIM:172800	Piebald trait		HP:0000598	OMIM:172800	IEA					P	HPO:iea[2009-02-17]
OMIM:172800	Piebald trait		HP:0000006	OMIM:172800	IEA					I	HPO:iea[2009-02-17]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0000132	PMID:15296495	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0001022	OMIM:614074	TAS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0003621	PMID:15296495	PCS		1/4			C	HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0000486	PMID:15296495	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0012805	PMID:15296495	PCS		4/4			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0003593	PMID:15296495	PCS		2/4			C	HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0003010	PMID:12548288	PCS		1/1		HP:0012826	P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0000639	PMID:15296495	PCS		2/4			P	HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0033263	PMID:15296495	PCS		3/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0007750	OMIM:614074	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0100608	PMID:15296495	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0000007	PMID:12548288	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0001107	PMID:12548288	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0007663	PMID:15296495	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0000978	PMID:15296495;PMID:12548288	PCS		4/4			P	HPO:probinson[2022-09-08];HPO:probinson[2013-08-10];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0000421	PMID:15296495	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0001873	PMID:15296495	PCS		0/4		HP:0012825	P	HPO:probinson[2013-08-10];HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0000666	OMIM:614074	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0004866	PMID:12548288	PCS		1/1			P	HPO:probinson[2022-09-08]
OMIM:614074	Hermansky-Pudlak syndrome 5		HP:0003623	PMID:15296495	PCS		1/4			C	HPO:probinson[2022-09-08]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0009738	OMIM:274205	TAS					P	HPO:skoehler[2015-07-18]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0000365	OMIM:274205	TAS					P	HPO:skoehler[2010-06-20]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0000518	OMIM:274205	TAS					P	HPO:iea[2009-02-17]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0001263	OMIM:274205	TAS					P	HPO:iea[2009-02-17]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0000007	OMIM:274205	TAS					I	HPO:iea[2009-02-17]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0009778	OMIM:274205	TAS					P	HPO:iea[2009-02-17]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0000028	OMIM:274205	TAS					P	HPO:iea[2009-02-17]
OMIM:274205	Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix,and deafness		HP:0000567	OMIM:274205	TAS					P	HPO:probinson[2015-07-18]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0007109	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0000540	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0011968	PMID:25008109	PCS		1/1			P	HPO:skoehler[2015-01-04]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0011924	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0002151	PMID:25008109	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0001252	PMID:25008109	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0001263	PMID:25008109	PCS		1/1			P	HPO:skoehler[2015-01-04]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0002490	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0032653	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0001943	PMID:25008109	PCS		1/1			P	HPO:skoehler[2015-01-04]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0000007	PMID:25008109	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0008897	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0001324	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0004900	PMID:25008109	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0003623	PMID:25008109	PCS		1/1			C	HPO:probinson[2023-03-22]
OMIM:616111	Mitochondrial complex III deficiency, nuclear type 9		HP:0003128	PMID:25008109	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-03-22]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:6001187	PMID:29053785	PCS					P	HPO:probinson[2025-09-26]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0002123	PMID:22608501	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0001272	PMID:22608501	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0001250	PMID:22608501	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0001251	PMID:22608501	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0025709	PMID:22608501	PCS		2/2			C	HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0012001	PMID:22608501	PCS		2/2			P	HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0000007	PMID:22608501	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0000648	PMID:22608501	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0000505	PMID:22608501	PCS		2/2		HP:0003676	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0001268	PMID:22608501	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0000556	PMID:22608501	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614706	Ceroid lipofuscinosis, neuronal, 11		HP:0003678	PMID:22608501	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:133690	Exostoses with anetodermia and brachydactyly, type E		HP:0002762	OMIM:133690	IEA					P	HPO:iea[2009-02-17]
OMIM:133690	Exostoses with anetodermia and brachydactyly, type E		HP:0004334	OMIM:133690	IEA					P	HPO:skoehler[2010-06-20]
OMIM:133690	Exostoses with anetodermia and brachydactyly, type E		HP:0005863	OMIM:133690	IEA					P	HPO:iea[2009-02-17]
OMIM:133690	Exostoses with anetodermia and brachydactyly, type E		HP:0000006	OMIM:133690	IEA					I	HPO:iea[2009-02-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0001771	PMID:16155110	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003236	PMID:16155110	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0000518	PMID:22187496	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0001324	PMID:25732997;PMID:22187496	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0002315	PMID:16155110	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003688	PMID:22187496	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0002017	PMID:16155110	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003326	PMID:16155110	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003689	PMID:22187496	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003348	PMID:22187496	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003546	PMID:16155110;PMID:25732997	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003202	PMID:22187496	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003200	PMID:22187496	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0030148	PMID:16155110	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003388	PMID:16155110;PMID:22187496	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0002151	PMID:16155110;PMID:25732997	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0002094	PMID:25732997	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0002490	PMID:25732997	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0012378	PMID:25732997	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0001639	PMID:25732997;PMID:22187496	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0001712	PMID:16155110;PMID:22187496	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0000007	PMID:16155110	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0008347	PMID:22187496	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0004900	PMID:22187496	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003677	PMID:22187496	PCS					C	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0001513	PMID:22187496	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-10-17]
OMIM:615418	Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)		HP:0003458	PMID:22187496	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:236750	Hydrops fetalis, nonimmune		HP:0003577	OMIM:236750	TAS					C	HPO:skoehler[2017-07-13]
OMIM:236750	Hydrops fetalis, nonimmune		HP:0001903	OMIM:236750	TAS	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:236750	Hydrops fetalis, nonimmune		HP:0001790	OMIM:236750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236750	Hydrops fetalis, nonimmune		HP:0001635	OMIM:236750	TAS	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:236750	Hydrops fetalis, nonimmune		HP:0001789	OMIM:236750	TAS	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:236750	Hydrops fetalis, nonimmune		HP:0010982	OMIM:236750	TAS					I	HPO:probinson[2024-08-03]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0001276	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0006989	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0003577	PMID:14757859	PCS		1/1			C	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0000089	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0003355	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0001371	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0002240	PMID:14757859	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0001508	PMID:14757859	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0003648	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0000278	OMIM:604273	IEA		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0000154	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0000252	OMIM:604273	IEA		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0002033	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0011925	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0002151	OMIM:604273	IEA		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0002490	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0011344	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0012385	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0011273	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0001838	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0003819	PMID:14757859	PCS		1/1			C	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0000426	OMIM:604273	IEA		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0000007	PMID:14757859	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0000347	PMID:14757859	PCS		1/1			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:604273	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1		HP:0003535	PMID:14757859	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-21]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000341	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0002465	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001773	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0004322	PMID:20358602	PCS					P	HPO:probinson[2013-02-17]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000463	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001156	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001250	OMIM:300590	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0002020	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0100543	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000319	PMID:22106055	PCS					P	HPO:probinson[2013-02-17]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000219	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0002119	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0009623	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0008897	OMIM:300590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0002714	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000218	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0030084	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001423	OMIM:300590	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001249	PMID:20358602	PCS					P	HPO:probinson[2013-02-17]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001007	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0002996	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0002553	PMID:22106055	PCS					P	HPO:probinson[2013-02-17]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000252	PMID:20358602	PCS					P	HPO:probinson[2013-02-17]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000494	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000574	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001263	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000470	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000294	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001419	PMID:20358602	PCS					I	HPO:probinson[2013-01-09]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001639	OMIM:300590	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000508	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000426	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000965	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000527	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0001511	PMID:20358602	PCS					P	HPO:probinson[2013-02-17]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000664	PMID:22106055	PCS					P	HPO:probinson[2013-02-17]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0200055	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000248	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300590	Cornelia de Lange syndrome 2		HP:0000347	OMIM:300590	TAS					P	HPO:skoehler[2015-11-15]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0002014	PMID:24156255	PCS		2/8			P	HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0012594	PMID:24156255	PCS		3/8			P	HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0100502	PMID:24156255	PCS		8/8			P	HPO:probinson[2020-07-19];HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0000010	PMID:24156255	PCS		1/8			P	HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0001903	PMID:24156255	PCS		5/8			P	HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0011463	PMID:24156255	PCS		8/8			C	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0000083	PMID:24156255	PCS		0/8			P	HPO:probinson[2020-07-19];HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0001889	PMID:24156255	PCS		2/8			P	HPO:probinson[2020-07-19]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0000007	PMID:24156255	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0008454	PMID:24156255	PCS		1/8			P	HPO:probinson[2024-03-16]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0000093	PMID:24156255	PCS		7/8			P	HPO:probinson[2020-07-19]
OMIM:618882	Imerslund-Grasbeck syndrome 2		HP:0001510	PMID:24156255	PCS		1/8			P	HPO:probinson[2024-03-16]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0004322	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000122	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001250	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001252	PMID:16236740	PCS		1/1			P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04];HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0010862	PMID:16236740	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001508	PMID:16236740	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0011463	PMID:16236740	PCS		1/1			C	HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000739	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0012450	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000337	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000238	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0002119	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000218	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000455	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001643	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000256	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000699	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001320	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000396	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000750	PMID:16236740	PCS		1/1			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001288	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0002079	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0011968	PMID:16236740	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000490	OMIM:609757	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001263	PMID:16236740	PCS		1/1			P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04];HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0011228	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0001518	PMID:16236740	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000729	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0011098	PMID:16236740	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000965	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000348	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000824	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000527	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000389	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0007018	PMID:16236740	PCS		1/1			P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04];HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000322	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000006	PMID:16236740	PCS					I	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04];HPO:probinson[2022-12-12]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000248	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000028	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000347	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000324	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:609757	Williams-Beuren region duplication syndrome		HP:0000126	OMIM:609637	TAS					P	HPO:skoehler[2016-02-25];HP:probinson[2019-01-04]
OMIM:611497	Osteopetrosis, autosomal recessive 6		HP:0011002	PMID:17404618	PCS		2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2021-03-12]
OMIM:611497	Osteopetrosis, autosomal recessive 6		HP:0000007	PMID:17404618	PCS					I	HPO:probinson[2013-01-09]
OMIM:611497	Osteopetrosis, autosomal recessive 6		HP:0100959	PMID:17404618	PCS	HP:0003593				P	HPO:probinson[2013-04-01]
OMIM:611497	Osteopetrosis, autosomal recessive 6		HP:0033701	PMID:17404618	PCS		1/1			P	HPO:probinson[2021-04-16]
OMIM:611497	Osteopetrosis, autosomal recessive 6		HP:0004975	PMID:17404618	PCS	HP:0003621				P	HPO:probinson[2013-04-01]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0000572	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0002059	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0003621	OMIM:610951	IEA					C	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0000750	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0002353	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0002123	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0001272	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0001263	OMIM:610951	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0000580	PMID:19277732	PCS					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0001251	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0002180	OMIM:610951	IEA					P	HPO:skoehler[2010-06-18]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0000618	OMIM:610951	IEA					P	HPO:skoehler[2010-06-18]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0000007	OMIM:610951	IEA					I	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0000648	OMIM:610951	IEA					P	HPO:iea[2009-02-17]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0000488	OMIM:610951	TAS					P	HPO:skoehler[2015-07-26]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0001268	OMIM:610951	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610951	Ceroid lipofuscinosis, neuronal, 7		HP:0003678	OMIM:610951	TAS					C	HPO:skoehler[2013-05-31]
OMIM:615829	Xia-Gibbs syndrome		HP:0002421	PMID:29230160	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0005656	PMID:24791903	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000483	PMID:35716097;PMID:30729726	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000365	PMID:35716097;PMID:31182893;PMID:30152016	PCS		3/8			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001212	PMID:24791903	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000486	PMID:35716097;PMID:27148574;PMID:34950897;PMID:29696776;PMID:30152016;PMID:39359946;PMID:33372375	PCS		11/25			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001057	PMID:35716097;PMID:30152016	PCS		3/15			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0004443	PMID:38357260	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0004322	PMID:35716097;PMID:38357260;PMID:27148574;PMID:30622101;PMID:34950897;PMID:30152016;PMID:29696776;PMID:34073322;PMID:39359946;PMID:30729726;PMID:33372375	PCS		18/43			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0004442	PMID:27148574;PMID:29230160;PMID:31182893	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002781	PMID:30152016	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0004440	PMID:31182893	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0025267	PMID:31182893;PMID:24791903	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0003593	PMID:35716097;PMID:30622101;PMID:34229113;PMID:30152016;PMID:34073322;PMID:39359946;PMID:30729726;PMID:33372375	PCS		14/25			C	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:6000995	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0033725	PMID:27148574;PMID:34229113;PMID:29696776;PMID:30152016;PMID:34073322;PMID:39359946;PMID:24791903;PMID:33372375	PCS		12/17			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000639	PMID:27148574	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000914	PMID:24791903	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002938	PMID:30152016	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000637	PMID:30622101;PMID:34950897;PMID:30729726;PMID:32256298	PCS		1/11			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002416	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002779	PMID:29230160;PMID:24791903	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000752	PMID:33372375	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000234	PMID:30152016	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002019	PMID:24791903	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001601	PMID:29230160;PMID:24791903	PCS		3/5			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0003623	PMID:35716097;PMID:36157999;PMID:34229113;PMID:31182893;PMID:29230160;PMID:30152016	PCS		11/22			C	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0003763	PMID:38357260;PMID:24791903	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000494	PMID:35716097;PMID:38357260;PMID:30622101;PMID:34229113;PMID:29230160;PMID:34950897;PMID:31182893;PMID:29696776;PMID:30152016;PMID:32256298;PMID:30729726;PMID:24791903	PCS		4/39			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000252	PMID:38357260;PMID:34950897;PMID:33372375	PCS		4/10			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001344	PMID:35716097;PMID:38357260;PMID:27148574;PMID:30622101;PMID:34229113;PMID:29696776;PMID:30152016;PMID:32256298;PMID:24791903	PCS		12/34			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:5201016	PMID:34229113	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0003487	PMID:38357260	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000490	PMID:34229113;PMID:34950897;PMID:29696776;PMID:30152016;PMID:32256298;PMID:30729726	PCS		6/29			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0100021	PMID:38357260;PMID:36157999;PMID:27148574;PMID:30622101;PMID:34950897;PMID:30152016;PMID:34073322;PMID:39359946;PMID:30729726;PMID:35716097;PMID:31182893;PMID:29230160;PMID:34229113;PMID:29696776;PMID:32256298;PMID:33372375;PMID:24791903	PCS		1/65			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0033454	PMID:24791903	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0010674	PMID:30152016	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001182	PMID:38357260;PMID:39359946;PMID:24791903	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000646	PMID:30729726	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000767	PMID:35716097;PMID:39359946	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0004209	PMID:35716097;PMID:34950897;PMID:30152016	PCS		3/12			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000520	PMID:36157999;PMID:31182893;PMID:30152016;PMID:30729726;PMID:32256298	PCS		4/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000006	PMID:24791903	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-30]
OMIM:615829	Xia-Gibbs syndrome		HP:0000248	PMID:36157999;PMID:34950897;PMID:31182893;PMID:39359946;PMID:32256298	PCS		3/13			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000369	PMID:38357260;PMID:35716097;PMID:34229113;PMID:34950897;PMID:31182893;PMID:29696776;PMID:30152016;PMID:34073322;PMID:30729726;PMID:24791903	PCS		13/41			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001336	PMID:32256298	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001276	PMID:31182893;PMID:30152016	PCS		6/11			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000341	PMID:38357260;PMID:36157999;PMID:31182893;PMID:30152016;PMID:39359946;PMID:32256298	PCS		2/16			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0003577	PMID:35716097;PMID:38357260;PMID:30152016;PMID:24791903	PCS		8/21			C	HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000582	PMID:35716097;PMID:38357260;PMID:30622101;PMID:29230160;PMID:34229113;PMID:34950897;PMID:31182893;PMID:29696776;PMID:30152016;PMID:30729726;PMID:32256298;PMID:24791903	PCS		14/40			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000343	PMID:35716097;PMID:38357260;PMID:36157999;PMID:31182893;PMID:30152016;PMID:39359946;PMID:32256298;PMID:30729726	PCS		6/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000463	PMID:35716097;PMID:29230160;PMID:34229113;PMID:39359946;PMID:32256298;PMID:30729726;PMID:24791903	PCS		5/13			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001156	PMID:30729726	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002365	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002000	PMID:30152016;PMID:30729726	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001274	PMID:34229113	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001273	PMID:30152016	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002240	PMID:24791903	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001270	PMID:38357260;PMID:30622101;PMID:34229113;PMID:30152016	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0010821	PMID:24791903	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0100704	PMID:27148574;PMID:30152016;PMID:24791903	PCS		4/19			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000739	PMID:38357260;PMID:30622101;PMID:30152016	PCS		5/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0100702	PMID:27148574;PMID:30729726	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000337	PMID:35716097;PMID:38357260;PMID:36157999;PMID:30622101;PMID:31182893;PMID:34229113;PMID:34950897;PMID:30152016;PMID:29696776;PMID:30729726;PMID:32256298	PCS		21/35			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0006970	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000219	PMID:38357260;PMID:36157999;PMID:34950897;PMID:30152016;PMID:39359946;PMID:30729726;PMID:35716097;PMID:31182893;PMID:34229113;PMID:29230160;PMID:29696776;PMID:32256298;PMID:33372375	PCS		25/39			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002119	PMID:39359946	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0030084	PMID:24791903;PMID:33372375	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000218	PMID:35716097;PMID:38357260;PMID:36157999;PMID:39359946;PMID:30729726;PMID:33372375;PMID:24791903	PCS		6/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000977	PMID:30622101;PMID:30152016	PCS		3/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0007269	PMID:24791903	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000455	PMID:30152016;PMID:39359946	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0006610	PMID:24791903	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000577	PMID:27148574;PMID:34229113;PMID:34073322	PCS		4/12			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002136	PMID:27148574	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002015	PMID:32256298	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000750	PMID:38357260;PMID:30622101;PMID:27148574;PMID:34950897;PMID:30152016;PMID:34073322;PMID:39359946;PMID:30729726;PMID:35716097;PMID:34229113;PMID:29230160;PMID:29696776;PMID:32256298;PMID:24791903	PCS		40/40			P	HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002650	PMID:35716097;PMID:27148574;PMID:30622101;PMID:34229113;PMID:34950897;PMID:29696776;PMID:30152016;PMID:34073322;PMID:39359946;PMID:32256298;PMID:24791903	PCS		16/39			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002376	PMID:27148574	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000232	PMID:38357260;PMID:36157999;PMID:39359946;PMID:30729726	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001288	PMID:27148574;PMID:24791903	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0005001	PMID:35716097;PMID:30152016;PMID:39359946	PCS		3/12			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001285	PMID:35716097;PMID:38357260;PMID:27148574;PMID:30622101;PMID:29696776;PMID:34073322;PMID:39359946	PCS		1/31			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000470	PMID:35716097;PMID:39359946	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0011228	PMID:29230160;PMID:31182893;PMID:30152016;PMID:32256298;PMID:30729726;PMID:24791903	PCS		6/15			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0010535	PMID:27148574;PMID:34229113;PMID:34950897;PMID:29696776;PMID:34073322;PMID:39359946;PMID:32256298	PCS		9/29			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0100710	PMID:27148574;PMID:34229113;PMID:33372375	PCS		3/6			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0031061	PMID:27148574	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0034295	PMID:27148574;PMID:29230160;PMID:39359946;PMID:30729726	PCS		4/11			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000508	PMID:35716097;PMID:27148574;PMID:34229113;PMID:29230160;PMID:31182893;PMID:30152016;PMID:29696776;PMID:32256298;PMID:30729726;PMID:24791903	PCS		14/41		HP:0012825	P	HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000348	PMID:35716097	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0008347	PMID:27148574	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0100716	PMID:38357260;PMID:30622101;PMID:27148574;PMID:31182893;PMID:34229113;PMID:30152016;PMID:33372375	PCS		9/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002007	PMID:36157999;PMID:30152016;PMID:39359946;PMID:32256298	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000347	PMID:38357260;PMID:36157999;PMID:34229113;PMID:29230160;PMID:31182893;PMID:29696776;PMID:39359946;PMID:30729726;PMID:32256298;PMID:24791903	PCS		12/27			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002643	PMID:31182893	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002069	PMID:30622101	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000286	PMID:29230160;PMID:30729726	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0005216	PMID:24791903	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002465	PMID:27148574;PMID:29230160	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001374	PMID:38357260	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0010804	PMID:38357260;PMID:36157999;PMID:31182893;PMID:34229113;PMID:29230160;PMID:39359946;PMID:32256298;PMID:30729726;PMID:33372375;PMID:24791903	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002067	PMID:32256298	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002188	PMID:35716097;PMID:34229113;PMID:39359946;PMID:24791903	PCS		7/10			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001256	PMID:38357260;PMID:35716097;PMID:30622101;PMID:34229113;PMID:31182893;PMID:30152016;PMID:33372375;PMID:24791903	PCS		4/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002342	PMID:35716097;PMID:38357260;PMID:30622101;PMID:31182893;PMID:34229113;PMID:30152016;PMID:33372375;PMID:24791903	PCS		8/13			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001773	PMID:35716097;PMID:30622101;PMID:24791903	PCS		4/6			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001250	PMID:27148574;PMID:34229113;PMID:34950897;PMID:29696776;PMID:39359946;PMID:32256298;PMID:24791903	PCS		14/30			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002066	PMID:38357260;PMID:35716097;PMID:30622101;PMID:27148574;PMID:34229113	PCS		5/13			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000160	PMID:38357260;PMID:36157999;PMID:30622101;PMID:29230160;PMID:39359946;PMID:32256298;PMID:24791903	PCS		1/11			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:24791903	PCS	HP:0003577	4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:27148574	PCS		6/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:35716097	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:32256298	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:38357260	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:29696776	PCS		12/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:29230160	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:39359946	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:30152016	PCS		9/10			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:34229113	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:30729726	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:34950897	PCS		6/8			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001252	PMID:36157999	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001251	PMID:27148574;PMID:34950897;PMID:29696776;PMID:32256298	PCS		14/23			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0004482	PMID:24791903	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000280	PMID:38357260;PMID:36157999;PMID:34950897;PMID:31182893;PMID:39359946;PMID:32256298;PMID:30729726	PCS		2/15			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0011463	PMID:35716097;PMID:32256298	PCS		2/6			C	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000319	PMID:38357260;PMID:35716097;PMID:36157999;PMID:31182893;PMID:34073322;PMID:39359946;PMID:30729726;PMID:32256298;PMID:33372375	PCS		5/14			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000718	PMID:38357260;PMID:30622101;PMID:34229113;PMID:29696776;PMID:32256298;PMID:33372375	PCS		7/23			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000717	PMID:35716097;PMID:27148574;PMID:34950897;PMID:29696776;PMID:34073322	PCS		11/28			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000316	PMID:35716097;PMID:34950897;PMID:34229113;PMID:29230160;PMID:29696776;PMID:30729726;PMID:32256298;PMID:24791903	PCS		14/35			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000954	PMID:35716097;PMID:34229113;PMID:30729726	PCS		5/8			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0025336	PMID:36157999;PMID:34229113;PMID:29230160;PMID:30152016;PMID:30729726;PMID:24791903;PMID:33372375	PCS		11/12			P	HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0006951	PMID:27148574;PMID:34229113;PMID:24791903	PCS		4/15			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001763	PMID:35716097;PMID:38357260;PMID:34229113;PMID:33372375	PCS		3/11			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001249	PMID:35716097;PMID:27148574;PMID:30152016;PMID:39359946;PMID:32256298;PMID:24791903	PCS		19/19			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0020206	PMID:38357260;PMID:30152016;PMID:30729726	PCS		2/8			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0003323	PMID:24791903	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000175	PMID:38357260;PMID:36157999;PMID:34950897;PMID:39359946;PMID:32256298;PMID:30729726	PCS		1/16			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000054	PMID:24791903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002353	PMID:27148574	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002870	PMID:35716097;PMID:38357260;PMID:30152016;PMID:24791903	PCS		8/9			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000211	PMID:24791903	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002079	PMID:38357260;PMID:30152016;PMID:24791903	PCS		7/9			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000331	PMID:36157999;PMID:30152016;PMID:32256298;PMID:30729726	PCS		2/12			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0025335	PMID:29230160	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0011968	PMID:35716097;PMID:27148574;PMID:30152016;PMID:24791903	PCS		10/15			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001382	PMID:35716097;PMID:27148574;PMID:34229113;PMID:30152016;PMID:39359946	PCS		17/18			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001263	PMID:38357260;PMID:36157999;PMID:27148574;PMID:30622101;PMID:30152016;PMID:34073322;PMID:39359946;PMID:30729726;PMID:35716097;PMID:29230160;PMID:34229113;PMID:29696776;PMID:32256298;PMID:24791903;PMID:33372375	PCS		54/54			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0012418	PMID:29230160	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0011448	PMID:38357260;PMID:36157999	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000729	PMID:35716097;PMID:38357260;PMID:27148574;PMID:34229113;PMID:31182893;PMID:30152016;PMID:24791903	PCS		10/15			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0007112	PMID:29230160	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001539	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0007874	PMID:34950897;PMID:32256298	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000565	PMID:27148574;PMID:34229113;PMID:29696776;PMID:34073322;PMID:24791903	PCS		8/26			P	ORCID:0000-0002-0736-9199[2025-03-05];HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];HPO:probinson[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0007754	PMID:27148574	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000289	PMID:35716097;PMID:39359946	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0007359	PMID:35716097	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001653	PMID:38357260;PMID:31182893;PMID:34073322;PMID:33372375	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000322	PMID:35716097;PMID:38357260;PMID:36157999;PMID:31182893;PMID:30152016;PMID:39359946;PMID:30729726;PMID:32256298;PMID:33372375	PCS		3/17			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0004887	PMID:29230160	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000687	PMID:38357260;PMID:30152016;PMID:24791903	PCS		5/9			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000385	PMID:34229113;PMID:29230160;PMID:29696776;PMID:39359946;PMID:32256298;PMID:30729726;PMID:24791903	PCS		3/23			P	HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000540	PMID:35716097;PMID:34229113;PMID:34950897;PMID:34073322;PMID:39359946;PMID:24791903	PCS		13/21			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000023	PMID:30152016;PMID:39359946	PCS		3/9			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0006808	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0011313	PMID:24791903	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002280	PMID:34073322;PMID:39359946	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0011318	PMID:30152016	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0010864	PMID:35716097;PMID:38357260;PMID:30622101;PMID:31182893;PMID:34229113;PMID:30152016;PMID:34073322;PMID:33372375	PCS		6/15			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001508	PMID:27148574;PMID:30152016;PMID:24791903	PCS		9/15			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001629	PMID:38357260;PMID:35716097;PMID:31182893;PMID:30152016;PMID:34073322;PMID:24791903	PCS		2/12			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0008551	PMID:38357260;PMID:31182893;PMID:34950897	PCS		2/11			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0009765	PMID:30152016	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000378	PMID:35716097;PMID:38357260;PMID:30152016	PCS		2/11			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000411	PMID:34229113;PMID:29696776;PMID:39359946;PMID:30729726;PMID:32256298;PMID:24791903	PCS		5/22			P	HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000256	PMID:38357260;PMID:30622101;PMID:34229113;PMID:34950897	PCS		6/13			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000396	PMID:30152016;PMID:39359946;PMID:32256298;PMID:30729726	PCS		2/13			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000154	PMID:30622101	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0002059	PMID:30622101;PMID:30152016	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001363	PMID:30152016;PMID:34073322	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0006913	PMID:29230160	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001762	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000431	PMID:34950897;PMID:39359946;PMID:30729726;PMID:32256298	PCS		1/12			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0031936	PMID:38357260;PMID:35716097;PMID:27148574;PMID:34950897;PMID:29230160;PMID:34229113;PMID:30152016;PMID:29696776;PMID:34073322;PMID:30729726;PMID:24791903;PMID:33372375	PCS		35/40			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001761	PMID:38357260;PMID:27148574;PMID:34229113;PMID:39359946;PMID:33372375	PCS		6/16			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000430	PMID:30152016;PMID:39359946;PMID:30729726	PCS		3/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0009909	PMID:35716097;PMID:29230160;PMID:29696776;PMID:39359946;PMID:32256298;PMID:30729726;PMID:24791903;PMID:33372375	PCS		6/25			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-30];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0045025	PMID:30622101	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0012510	PMID:27148574	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0005280	PMID:31182893;PMID:34229113;PMID:29230160;PMID:29696776;PMID:34073322;PMID:39359946;PMID:32256298;PMID:30729726;PMID:24791903	PCS		14/26			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0011396	PMID:27148574	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0007334	PMID:34073322	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000389	PMID:24791903	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000268	PMID:38357260	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001511	PMID:35716097	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001357	PMID:35716097;PMID:30152016;PMID:24791903	PCS		4/12			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0200055	PMID:24791903	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000664	PMID:35716097;PMID:30152016;PMID:32256298	PCS		3/8			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0001631	PMID:35716097;PMID:38357260;PMID:27148574;PMID:31182893;PMID:30152016;PMID:34073322	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0000028	PMID:35716097;PMID:27148574	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:615829	Xia-Gibbs syndrome		HP:0009879	PMID:34229113;PMID:24791903	PCS		3/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30];HPO:probinson[2025-03-05];ORCID:0000-0002-0736-9199[2025-03-05]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0002067	PMID:22341972	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0001410	PMID:22341972	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0001300	OMIM:613280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0003376	OMIM:613280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0001332	PMID:22341972	PCS		14/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0025196	PMID:22341972	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0001260	PMID:22341972	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0002063	OMIM:613280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0001394	PMID:22341972	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0002240	PMID:22341972	PCS		5/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0002172	OMIM:613280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0002071	PMID:22341972	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0008282	PMID:22341972	PCS					P	HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0007141	OMIM:613280	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0032097	PMID:22341972	PCS		15/15			P	HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0007010	OMIM:613280	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0000007	PMID:22341972	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0001901	PMID:22341972	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0002910	PMID:22341972	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0002313	PMID:22341972	PCS		1/15			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-07-10]
OMIM:613280	Hypermanganesemia with dystonia 1		HP:0001337	OMIM:613280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619975	Tumor predisposition syndrome 2		HP:0005227	PMID:31322271	PCS	HP:0003596	1/1			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0005227	PMID:30049810	PCS		2/3			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0005227	PMID:35460607	PCS		7/7			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0003621	PMID:35460607	PCS		1/7			C	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0003596	PMID:31322271;PMID:35460607	PCS		4/9			C	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0007716	PMID:35460607	PCS		2/8			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0003003	PMID:31322271	PCS	HP:0003596	1/1			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0003003	PMID:35460607	PCS		1/8			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0004808	PMID:30049810	PCS	HP:0011462	3/3			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0004808	PMID:35460607	PCS		4/8			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0011462	PMID:30049810;PMID:35460607	PCS		7/10			C	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0100008	PMID:35460607	PCS		1/8			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0031919	PMID:35460607	PCS		1/4			P	HPO:probinson[2022-09-05];HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0002858	PMID:35460607	PCS		1/8			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0030075	PMID:35460607	PCS		1/4			P	HPO:probinson[2022-09-05]
OMIM:619975	Tumor predisposition syndrome 2		HP:0000006	PMID:31322271	PCS					I	HPO:probinson[2022-09-05]
OMIM:300779	Corneal dystrophy, endothelial, X-linked		HP:0007957	OMIM:300779	TAS	HP:0003577				P	HPO:skoehler[2014-01-28]
OMIM:300779	Corneal dystrophy, endothelial, X-linked		HP:0000585	OMIM:300779	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300779	Corneal dystrophy, endothelial, X-linked		HP:0001131	OMIM:300779	IEA					P	HPO:skoehler[2015-01-19]
OMIM:300779	Corneal dystrophy, endothelial, X-linked		HP:0001423	OMIM:300779	TAS					I	HPO:skoehler[2014-01-28]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0002960	OMIM:617780	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0000365	OMIM:617780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0001894	OMIM:617780	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0001250	PMID:21813566	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0003593	PMID:21813566	PCS		1/1			C	HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0003095	OMIM:617780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0002160	PMID:21813566	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0002719	OMIM:617780	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0001889	PMID:21813566	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0001888	PMID:21813566	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0006532	OMIM:617780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0025435	PMID:21813566	PCS		2/2			P	HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0025517	PMID:21813566	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0004313	PMID:21813566	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0003223	OMIM:617780	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0002013	OMIM:617780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0004430	PMID:21813566	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0010972	OMIM:617780	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0000007	PMID:21813566	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0000964	OMIM:617780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0001972	OMIM:617780	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0001876	PMID:21813566	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-15]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0025406	OMIM:617780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617780	Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia		HP:0004821	PMID:21813566	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:166450	OSTEOMESOPYKNOSIS		HP:0011001	OMIM:166450	TAS					P	HPO:probinson[2009-02-17]
OMIM:166450	OSTEOMESOPYKNOSIS		HP:0000789	OMIM:166450	IEA					P	HPO:iea[2009-02-17]
OMIM:166450	OSTEOMESOPYKNOSIS		HP:0003419	OMIM:166450	IEA					P	HPO:iea[2009-02-17]
OMIM:166450	OSTEOMESOPYKNOSIS		HP:0000006	OMIM:166450	IEA					I	HPO:iea[2009-02-17]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003202	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003621	PMID:34581780	PCS		1/7			C	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003236	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003687	PMID:35915960	PCS	HP:0003581	1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003201	PMID:35915960;PMID:34581780	PCS		5/8			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0008959	PMID:35915960	PCS	HP:0003581	1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003593	PMID:34581780	PCS		1/7			C	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0001270	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0100297	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0009073	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0011463	PMID:35915960;PMID:34581780	PCS		6/8			C	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003738	PMID:35915960;PMID:34581780	PCS		6/8			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0002913	PMID:35915960	PCS		0/1			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0000007	PMID:34581780	PCS					I	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0025435	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003701	PMID:34581780	PCS		5/7		HP:0012825	P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003713	PMID:34581780	PCS		2/2			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0002910	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003259	PMID:34581780	PCS	HP:0003581	7/7			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003710	PMID:35915960;PMID:34581780	PCS		3/8			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0008967	PMID:34581780	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003557	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620138	Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis		HP:0003546	PMID:35915960	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:207770	Aprosencephaly syndrome		HP:0002323	OMIM:207770	IEA					P	HPO:iea[2009-02-17]
OMIM:207770	Aprosencephaly syndrome		HP:0000007	OMIM:207770	IEA					I	HPO:iea[2009-02-17]
OMIM:207770	Aprosencephaly syndrome		HP:0007268	OMIM:207770	IEA					P	HPO:iea[2009-02-17]
OMIM:207770	Aprosencephaly syndrome		HP:0009380	OMIM:207770	IEA					P	HPO:iea[2009-02-17]
OMIM:251250	Microcephaly with cervical spine fusion anomalies		HP:0000252	OMIM:251250	IEA					P	HPO:iea[2009-02-17]
OMIM:251250	Microcephaly with cervical spine fusion anomalies		HP:0004322	OMIM:251250	IEA					P	HPO:iea[2009-02-17]
OMIM:251250	Microcephaly with cervical spine fusion anomalies		HP:0002176	OMIM:251250	IEA					P	HPO:iea[2009-02-17]
OMIM:251250	Microcephaly with cervical spine fusion anomalies		HP:0002948	OMIM:251250	IEA					P	HPO:iea[2009-02-17]
OMIM:251250	Microcephaly with cervical spine fusion anomalies		HP:0005881	OMIM:251250	IEA					P	HPO:iea[2009-02-17]
OMIM:251250	Microcephaly with cervical spine fusion anomalies		HP:0000007	OMIM:251250	IEA					I	HPO:iea[2009-02-17]
OMIM:251250	Microcephaly with cervical spine fusion anomalies		HP:0001249	OMIM:251250	IEA					P	HPO:iea[2009-02-17]
OMIM:118830	Chylomicronemia, familial, due to circulating inhibitor of lipoproteinlipase		HP:0100027	OMIM:118830	TAS					P	HPO:probinson[2012-07-19]
OMIM:118830	Chylomicronemia, familial, due to circulating inhibitor of lipoproteinlipase		HP:0010980	OMIM:118830	TAS					P	HPO:probinson[2012-07-19]
OMIM:118830	Chylomicronemia, familial, due to circulating inhibitor of lipoproteinlipase		HP:0000006	OMIM:118830	TAS					I	HPO:probinson[2009-02-17]
OMIM:118830	Chylomicronemia, familial, due to circulating inhibitor of lipoproteinlipase		HP:0001744	OMIM:118830	TAS					P	HPO:probinson[2009-02-17]
OMIM:118830	Chylomicronemia, familial, due to circulating inhibitor of lipoproteinlipase		HP:0002027	OMIM:118830	TAS					P	HPO:skoehler[2010-06-20]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001374	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000343	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000486	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000463	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000023	OMIM:219200	IEA					P	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001250	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000260	PMID:22773132	PCS		12/12			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-22]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000160	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001252	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0003196	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001290	OMIM:219200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001270	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0012368	OMIM:219200	TAS					P	HPO:skoehler[2013-10-22]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001508	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001305	OMIM:219200	TAS					P	HPO:skoehler[2013-04-02]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0008872	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0009125	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000218	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001302	OMIM:219200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001763	OMIM:219200	IEA					P	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001249	PMID:22773132	PCS		4/13			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-22]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000973	OMIM:219200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000670	OMIM:219200	IEA					P	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000494	OMIM:219200	IEA					P	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000252	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0002650	OMIM:219200	IEA					P	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0002299	OMIM:219200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001382	PMID:22773132	PCS		11/12			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-22]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0010719	OMIM:219200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001582	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000272	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0011800	OMIM:219200	TAS					P	HPO:skoehler[2013-11-28]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0003160	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0007392	PMID:22773132	PCS		13/13			P	HPO:probinson[2022-12-22]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000007	OMIM:219200	IEA					I	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0002208	OMIM:219200	TAS					P	HPO:skoehler[2013-04-02]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0002007	OMIM:219200	IEA					P	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0001511	OMIM:219200	IEA					P	HPO:iea[2009-02-17]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000369	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0000545	OMIM:219200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219200	Cutis laxa, autosomal recessive, type IIA		HP:0002126	OMIM:219200	TAS					P	HPO:skoehler[2013-04-02]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0003621	PMID:16917026	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0003388	OMIM:254300	IEA					P	HPO:iea[2009-02-17]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0003473	PMID:16917026	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0003693	OMIM:254300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0001283	OMIM:254300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0002792	PMID:16917026	PCS		4/10			P	HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0003394	OMIM:254300	IEA					P	HPO:iea[2009-02-17]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0003391	OMIM:254300	IEA					P	HPO:iea[2009-02-17]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0030319	PMID:16917026	PCS		19/19			P	HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0030208	PMID:16917026	PCS		0/19			P	HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0008180	OMIM:254300	IEA					P	HPO:iea[2009-02-17]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0012473	PMID:16917026	PCS		4/10			P	HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0011463	PMID:16917026	PCS					C	HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0000508	PMID:16917026	PCS		13/19			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0001558	OMIM:254300	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0000007	OMIM:254300	IEA					I	HPO:iea[2009-02-17]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0002515	OMIM:254300	IEA					P	HPO:iea[2009-02-17]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0002747	OMIM:254300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0007126	OMIM:254300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0003327	PMID:16917026	PCS		16/18			P	HPO:probinson[2022-07-01]
OMIM:254300	Myasthenia, limb-girdle, familial		HP:0000597	OMIM:254300	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:619949	Spermatogenic failure 75		HP:0003251	PMID:32741963	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:619949	Spermatogenic failure 75		HP:0011462	PMID:32741963	PCS		2/2			C	HPO:probinson[2022-08-20]
OMIM:619949	Spermatogenic failure 75		HP:0008232	PMID:32741963	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:619949	Spermatogenic failure 75		HP:0000007	PMID:32741963	PCS					I	HPO:probinson[2022-08-20]
OMIM:619949	Spermatogenic failure 75		HP:0011961	PMID:32741963	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:619949	Spermatogenic failure 75		HP:0031039	PMID:32741963	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001276	PMID:29186371	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0003577	PMID:29186371	PCS		1/4			C	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0000640	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0002188	PMID:29186371	PCS		4/4			P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001332	PMID:29186371	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001310	PMID:29186371	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0002362	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001250	PMID:29186371	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0002066	PMID:29186371	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001252	PMID:29186371	PCS		2/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001152	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0003593	PMID:29186371	PCS		3/4			C	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0010544	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0002080	PMID:29186371	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0000639	PMID:29186371	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001508	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0002415	PMID:29186371	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001249	PMID:29186371	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001348	PMID:29186371	PCS		2/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001347	PMID:29186371	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001583	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0002136	PMID:29186371	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0000750	PMID:29186371	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001344	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0002079	PMID:29186371	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0031936	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001266	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0011968	PMID:29186371	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001260	PMID:29186371	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0001263	PMID:29186371	PCS		2/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0000709	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0012043	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0007256	PMID:29186371	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0025403	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0000543	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0007811	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0000666	PMID:29186371	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617964	Leukodystrophy, hypomyelinating, 16		HP:0000006	PMID:29186371	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:163500	Night blindness, congenital stationary, autosomal dominant 2		HP:0001098	PMID:8075643	PCS		0/1			P	HPO:probinson[2015-06-02];HPO:probinson[2024-03-16]
OMIM:163500	Night blindness, congenital stationary, autosomal dominant 2		HP:0007663	PMID:8075643	PCS		0/1			P	HPO:probinson[2024-03-16]
OMIM:163500	Night blindness, congenital stationary, autosomal dominant 2		HP:0007642	OMIM:163500	TAS		1/1			P	HPO:probinson[2009-02-17]
OMIM:163500	Night blindness, congenital stationary, autosomal dominant 2		HP:0000006	PMID:8075643	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:163500	Night blindness, congenital stationary, autosomal dominant 2		HP:0031624	PMID:8075643	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0003577	PMID:15114530	PCS		1/1			C	HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000463	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0001250	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:6000752	PMID:15114530	PCS		1/1			P	HPO:probinson[2024-06-29]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0001252	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000063	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0011220	PMID:15114530	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0001943	PMID:15114530	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000219	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000154	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0001684	PMID:15114530	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0005487	PMID:15114530	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0034565	PMID:15114530	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0010781	PMID:15114530	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0002902	PMID:15114530	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000426	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000007	PMID:15114530	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000648	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0008665	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0007875	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0002007	OMIM:608688	IEA					P	HPO:iea[2009-02-17]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000565	PMID:15114530	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000248	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:608688	AICA-ribosiduria due to ATIC deficiency		HP:0000369	PMID:15114530	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0004840	PMID:1570328	PCS		1/1	MALE		P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0001419	PMID:1570328	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2022-08-21]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0011463	PMID:1570328	PCS		1/1			C	HPO:probinson[2022-08-21]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0010972	PMID:1570328	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-21]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0001924	PMID:1570328	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-21]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0001972	OMIM:300751	IEA			FEMALE		P	HPO:skoehler[2010-06-20]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0025406	PMID:1570328	PCS		1/1			P	HPO:probinson[2022-08-21]
OMIM:300751	Anemia, sideroblastic, X-linked		HP:0001017	PMID:1570328	PCS		1/1			P	HPO:probinson[2022-08-21]
OMIM:620104	Amelogenesis imperfecta, type IK		HP:0000705	PMID:32167558	PCS		10/10			P	HPO:probinson[2022-11-25]
OMIM:620104	Amelogenesis imperfecta, type IK		HP:0006297	PMID:32167558	PCS		10/10			P	HPO:probinson[2022-11-25]
OMIM:620104	Amelogenesis imperfecta, type IK		HP:0000006	PMID:32167558	PCS					I	HPO:probinson[2022-11-25]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0030666	PMID:12714659	PCS		3/10			P	HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0003621	PMID:21179233	PCS		2/2			C	HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0000551	PMID:12714659	PCS		4/8			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0030499	PMID:12714659	PCS		7/10			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0030631	PMID:12714659	PCS		2/3			P	HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0007663	PMID:12714659	PCS		4/8			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0000603	PMID:12714659	PCS		2/7			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0007722	PMID:12714659	PCS		6/10			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0000006	PMID:12714659	PCS					I	HPO:probinson[2017-06-23];HPO:probinson[2024-03-16]
OMIM:608850	Macular dystrophy, retinal, 3		HP:0000512	PMID:12714659	PCS		0/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-16]
OMIM:619785	Epidermolysis bullosa, junctional 3A, intermediate		HP:0003577	PMID:11564184	PCS		1/1			C	HPO:probinson[2022-05-11]
OMIM:619785	Epidermolysis bullosa, junctional 3A, intermediate		HP:0003341	PMID:11564184	IEA		1/1			P	HPO:probinson[2022-05-11]
OMIM:619785	Epidermolysis bullosa, junctional 3A, intermediate		HP:0008066	PMID:11564184;PMID:11810295	PCS		2/2			P	HPO:probinson[2022-05-11]
OMIM:619785	Epidermolysis bullosa, junctional 3A, intermediate		HP:0000007	PMID:11810295	PCS					I	HPO:probinson[2022-05-11];HPO:probinson[2022-05-11]
OMIM:619785	Epidermolysis bullosa, junctional 3A, intermediate		HP:0200097	PMID:11564184	PCS		0/1			P	HPO:probinson[2022-05-11]
OMIM:619785	Epidermolysis bullosa, junctional 3A, intermediate		HP:0020117	PMID:11564184;PMID:11810295	PCS		2/2			P	HPO:probinson[2022-05-11]
OMIM:300989	Meester-Loeys syndrome		HP:0001058	PMID:27632686	PCS		1/5			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0004322	PMID:27632686	PCS		5/11			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001156	PMID:27632686	PCS		3/7			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001373	PMID:27632686	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0004482	PMID:27632686	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0010646	PMID:27632686	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000998	PMID:27632686	PCS		2/3			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000316	PMID:27632686	PCS		8/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0002616	PMID:27632686	PCS		13/15			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0004937	PMID:27632686	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0002119	PMID:27632686	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000978	PMID:27632686	PCS		1/5			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000218	PMID:27632686	PCS		2/5			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001763	PMID:27632686	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000212	PMID:27632686	PCS		2/3			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001166	PMID:27632686	PCS		4/10			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000494	PMID:27632686	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001382	PMID:27632686	PCS		8/10			P	HPO:skoehler[2017-07-13]
OMIM:300989	Meester-Loeys syndrome		HP:0004970	PMID:27632686	PCS		2/5			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000193	PMID:27632686	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001065	PMID:27632686	PCS		4/9			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000272	PMID:27632686	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0012385	PMID:27632686	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0034392	PMID:27632686	PCS		4/7			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001537	PMID:27632686	PCS		1/6			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000766	PMID:27632686	PCS		4/10			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0002647	PMID:27632686	PCS		3/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001417	PMID:27632686	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0002007	PMID:27632686	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000268	PMID:27632686	PCS		4/7			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0000520	PMID:27632686	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0004944	PMID:27632686	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0009836	PMID:27632686	PCS		3/6			P	HPO:probinson[2023-02-22]
OMIM:300989	Meester-Loeys syndrome		HP:0001634	PMID:27632686	PCS		1/15			P	HPO:probinson[2023-02-22]
OMIM:617970	Rh-null disease, amorph type		HP:0005502	OMIM:617970	TAS					P	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:617970	Rh-null disease, amorph type		HP:0004446	OMIM:617970	TAS					P	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:617970	Rh-null disease, amorph type		HP:0011273	OMIM:617970	TAS					P	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:617970	Rh-null disease, amorph type		HP:0002904	OMIM:617970	TAS					P	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:617970	Rh-null disease, amorph type		HP:0001878	PMID:25413218	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:617970	Rh-null disease, amorph type		HP:0000007	PMID:9657769	PCS					I	HPO:probinson[2024-03-01]
OMIM:617970	Rh-null disease, amorph type		HP:0001923	OMIM:617970	TAS					P	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:167000	Ovarian cancer		HP:0003002	OMIM:167000	IEA					P	HPO:iea[2009-02-17]
OMIM:167000	Ovarian cancer		HP:0100621	OMIM:167000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:167000	Ovarian cancer		HP:0001442	OMIM:167000	IEA					I	HPO:skoehler[2019-04-18]
OMIM:167000	Ovarian cancer		HP:0006774	OMIM:167000	IEA					P	HPO:iea[2009-02-17]
OMIM:167000	Ovarian cancer		HP:0000006	OMIM:167000	IEA					I	HPO:iea[2009-02-17]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000286	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000483	PMID:36208065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0005930	PMID:28488351;PMID:37352860	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000486	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0004288	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0010049	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0010047	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0008093	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001849	PMID:28488351;PMID:37352860	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001804	PMID:28488351;PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0011463	PMID:37352860	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000717	PMID:36208065;PMID:28488351;PMID:37352860	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001845	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001802	PMID:28488351;PMID:37352860	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001769	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000358	PMID:36208065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001249	PMID:36208065;PMID:28488351;PMID:37352860	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0003468	PMID:28488351	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0002553	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0002750	PMID:37352860	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001263	PMID:36208065;PMID:28488351;PMID:37352860	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000294	PMID:28488351;PMID:37352860	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0004570	PMID:37352860	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0009890	PMID:28488351;PMID:37352860	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0002827	PMID:37352860	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000926	PMID:37352860	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000767	PMID:37352860	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000007	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001814	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000768	PMID:37352860	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0004209	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000960	PMID:36208065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000369	PMID:36208065;PMID:28488351;PMID:37352860	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000325	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000248	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000126	PMID:28488351;PMID:37352860	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0004689	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000341	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0003577	PMID:36208065;PMID:28488351;PMID:37352860	PCS		4/5			C	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:6000891	PMID:36208065	PCS		1/1			P	HPO:probinson[2024-08-04];HPO:probinson[2024-08-04]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001156	PMID:28488351;PMID:37352860	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000023	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000938	PMID:37352860	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0011682	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0008079	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0009882	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0002999	PMID:37352860	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000218	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000378	PMID:37352860	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000076	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000750	PMID:36208065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000431	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0002650	PMID:37352860	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0009909	PMID:37352860	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0009276	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000508	PMID:36208065;PMID:28488351	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000307	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000944	PMID:28488351;PMID:37352860	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0004704	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001159	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0002645	PMID:37352860	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000465	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0001631	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0000545	PMID:36208065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0009638	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0004425	PMID:28488351	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:620662	Hoxha-Aliu syndrome		HP:0004227	PMID:37352860	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-15]
OMIM:211890	Campomelia, Cumming type		HP:0004322	OMIM:211890	IEA					P	HPO:iea[2009-02-17]
OMIM:211890	Campomelia, Cumming type		HP:0000007	OMIM:211890	TAS					I	HPO:iea[2009-02-17]
OMIM:211890	Campomelia, Cumming type		HP:0001748	OMIM:211890	IEA					P	HPO:iea[2009-02-17]
OMIM:211890	Campomelia, Cumming type		HP:0006487	OMIM:211890	TAS					P	HPO:iea[2012-07-16]
OMIM:211890	Campomelia, Cumming type		HP:0001737	OMIM:211890	TAS					P	HPO:iea[2012-07-16]
OMIM:211890	Campomelia, Cumming type		HP:0000476	OMIM:211890	IEA					P	HPO:skoehler[2010-06-20]
OMIM:211890	Campomelia, Cumming type		HP:0001004	OMIM:211890	IEA					P	HPO:skoehler[2010-06-20]
OMIM:211890	Campomelia, Cumming type		HP:0000113	OMIM:211890	TAS					P	HPO:skoehler[2012-10-17]
OMIM:211890	Campomelia, Cumming type		HP:0006557	OMIM:211890	TAS					P	HPO:iea[2009-02-17]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0003621	PMID:24459106	PCS		2/6			C	HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0033748	PMID:24459106	PCS		4/5			P	HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0003390	PMID:24459106	PCS		4/4			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0041162	PMID:24459106	PCS		5/7			P	HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0009771	OMIM:615632	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0011462	PMID:24459106	PCS		4/6			C	HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0001822	PMID:24459106	PCS		6/7			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0002821	PMID:24459106	PCS		5/7			P	HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0000006	PMID:24459106	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0002600	PMID:24459106	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0002754	OMIM:615632	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0000962	OMIM:615632	TAS					P	HPO:skoehler[2014-02-25];HPO:probinson[2023-02-26]
OMIM:615632	Neuropathy, hereditary sensory, type IF		HP:0007328	PMID:24459106	PCS		6/7			P	HPO:probinson[2023-02-26]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0003621	PMID:18572189	IEA		2/4			C	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0001663	OMIM:613243	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0003596	PMID:11385718;PMID:18572189	PCS		2/5			C	HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0005157	PMID:11385718	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0200128	OMIM:613243	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0001681	PMID:18572189	PCS		2/4			P	HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0005110	PMID:11385718;PMID:18572189	PCS		1/5			P	HPO:probinson[2022-07-04];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0011711	PMID:11385718	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0002094	PMID:11385718	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0011712	PMID:11385718	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0012664	PMID:11385718	PCS		0/1			P	HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0001639	PMID:18572189	PCS		4/4			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0012250	OMIM:613243	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0011462	PMID:18572189	PCS		1/4			C	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0100749	PMID:18572189	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0001279	PMID:18572189	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-04]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0000006	OMIM:613243	TAS					I	HPO:skoehler[2017-07-13]
OMIM:613243	Cardiomyopathy, familial hypertrophic, 13		HP:0002875	PMID:11385718	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:600559	Hydrocephalus, endocardial fibroelastosis, and cataracts		HP:0001561	OMIM:600559	IEA					P	HPO:iea[2009-02-17]
OMIM:600559	Hydrocephalus, endocardial fibroelastosis, and cataracts		HP:0001706	OMIM:600559	IEA					P	HPO:iea[2009-02-17]
OMIM:600559	Hydrocephalus, endocardial fibroelastosis, and cataracts		HP:0000519	OMIM:600559	IEA					P	HPO:iea[2009-02-17]
OMIM:600559	Hydrocephalus, endocardial fibroelastosis, and cataracts		HP:0001522	OMIM:600559	IEA					C	HPO:iea[2009-02-17]
OMIM:600559	Hydrocephalus, endocardial fibroelastosis, and cataracts		HP:0001334	OMIM:600559	IEA					P	HPO:iea[2009-02-17]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002069	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000486	PMID:30526868	PCS		2/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002263	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0003196	PMID:30526868	PCS		8/10			P	HPO:probinson[2022-11-23];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0030451	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002020	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001290	PMID:30526868	PCS		2/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000319	PMID:30526868	PCS		1/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000316	PMID:30526868	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001845	PMID:30526868	PCS		2/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001328	PMID:30526868	PCS		10/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000998	PMID:30526868	PCS		10/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0100807	PMID:30526868	PCS		3/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0008577	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001643	PMID:30526868	PCS		3/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000358	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0009748	PMID:30526868	PCS		10/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002553	PMID:30526868	PCS		10/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000490	PMID:30526868	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001263	PMID:30526868	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0010511	PMID:30526868	PCS		2/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0010557	OMIM:618316	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0011571	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000448	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000767	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000007	PMID:30526868	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001539	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000047	PMID:30526868	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000322	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0007359	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000369	PMID:30526868	PCS		8/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000325	PMID:30526868	PCS		10/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001655	OMIM:618316	IEA		1/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0003577	PMID:30526868	PCS		10/10			C	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002089	OMIM:618316	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000343	PMID:30526868	PCS		7/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000463	PMID:30526868	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0012725	OMIM:618316	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001270	PMID:30526868	PCS		9/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001629	PMID:30526868	PCS		6/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000219	PMID:30526868	PCS		6/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0004935	PMID:30526868	PCS		1/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0006610	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000256	PMID:30526868	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000750	PMID:30526868	PCS		10/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002650	PMID:30526868	PCS		3/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000431	OMIM:618316	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0031936	PMID:30526868	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0005280	PMID:30526868	PCS		8/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001719	PMID:30526868	PCS		2/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0007099	PMID:30526868	PCS		1/7			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001636	PMID:30526868	PCS		2/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000307	PMID:30526868	PCS		10/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000664	PMID:30526868	PCS		10/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002205	PMID:30526868	PCS		2/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0001631	PMID:30526868	PCS		6/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000465	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000028	PMID:30526868	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0000545	PMID:30526868	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-23]
OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies		HP:0002566	PMID:30526868	PCS		1/10			P	HPO:probinson[2022-11-23]
OMIM:617025	Nevus comedonicus, somatic		HP:0001442	PMID:27153399	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-07]
OMIM:617025	Nevus comedonicus, somatic		HP:0020154	PMID:27153399	PCS					P	HPO:probinson[2019-09-07]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0002069	PMID:31257402	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0002268	PMID:31257402	PCS	HP:0011463	6/6		HP:0025377	P	HPO:probinson[2013-02-27];HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0002356	PMID:31257402	PCS		3/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0002378	PMID:31257402	PCS		5/6			P	HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0001260	PMID:31257402	PCS		2/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0003593	PMID:31257402	PCS		2/6			C	HPO:probinson[2009-02-17];HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0000639	PMID:31257402	PCS		3/6			P	HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0011463	PMID:31257402	PCS		4/6			C	HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0011153	PMID:31257402	PCS		6/6			P	HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0007332	OMIM:608105	TAS					P	HPO:probinson[2009-02-17]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0000007	PMID:31257402	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-10-23]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0007104	OMIM:608105	TAS					P	HPO:probinson[2009-02-17]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0000666	OMIM:608105	TAS					P	HPO:probinson[2009-02-17]
OMIM:608105	Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp		HP:0001336	OMIM:608105	IEA					P	HPO:skoehler[2019-09-07]
OMIM:273740	Thoracomelic dysplasia		HP:0001591	OMIM:273740	IEA					P	HPO:iea[2009-02-17]
OMIM:273740	Thoracomelic dysplasia		HP:0008873	OMIM:273740	IEA					P	HPO:iea[2009-02-17]
OMIM:273740	Thoracomelic dysplasia		HP:0000007	OMIM:273740	IEA					I	HPO:iea[2009-02-17]
OMIM:273740	Thoracomelic dysplasia		HP:0000773	OMIM:273740	IEA					P	HPO:iea[2009-02-17]
OMIM:620851	ReNU syndrome		HP:0001298	PMID:38991538	PCS		0/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002389	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0004322	PMID:38859706;PMID:38991538	PCS		38/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002020	PMID:38859706;PMID:38991538;PMID:39369315	PCS		26/55			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012506	PMID:38991538	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0006191	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000639	PMID:38991538;PMID:39369315	PCS		25/51			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0007165	PMID:38991538	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000879	PMID:38859706;PMID:38991538	PCS		6/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000873	PMID:38991538;PMID:39369315	PCS		12/53			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002019	PMID:38991538;PMID:39369315	PCS		35/55			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001048	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0033454	PMID:38859706;PMID:38991538;PMID:39369315	PCS		15/53			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0100021	PMID:38859706;PMID:38991538	PCS		9/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001182	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001181	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000767	PMID:39369315	PCS		0/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000403	PMID:39369315	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000527	PMID:38859706;PMID:38991538	PCS		4/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000768	PMID:39369315	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000400	PMID:38991538	PCS		3/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000189	PMID:39369315	PCS		7/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002002	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002360	PMID:38991538;PMID:39369315	PCS		5/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001270	PMID:39369315	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012169	PMID:38991538	PCS		11/48			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000737	PMID:38991538;PMID:39369315	PCS		4/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0100702	PMID:38991538	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000618	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000739	PMID:38991538	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0006970	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000733	PMID:38991538;PMID:39369315	PCS		11/16			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002119	PMID:38991538;PMID:39369315	PCS		8/55			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000736	PMID:39369315	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000179	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001166	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002015	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002136	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000750	PMID:38991538;PMID:39369315	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001288	PMID:38991538;PMID:39369315	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002376	PMID:39369315	PCS		0/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000194	PMID:38991538;PMID:39369315	PCS		13/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000193	PMID:38991538	PCS		1/40			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0032388	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0034323	PMID:38991538	PCS		11/33			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0031061	PMID:39369315	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0010782	PMID:38859706;PMID:38991538	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000506	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0034454	PMID:38991538	PCS		3/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0030890	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0100716	PMID:38991538	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0200096	PMID:38991538	PCS		1/40			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000286	PMID:38991538;PMID:39369315	PCS		13/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001250	PMID:38859706;PMID:38991538;PMID:39369315	PCS		45/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000160	PMID:38859706;PMID:38991538	PCS		2/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001252	PMID:38859706;PMID:38991538;PMID:39369315	PCS		42/48			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001251	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011856	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000718	PMID:38991538;PMID:39369315	PCS		3/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0007002	PMID:38991538	PCS		3/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000954	PMID:38859706;PMID:38991538;PMID:39369315	PCS		11/61			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000158	PMID:38859706;PMID:38991538	PCS		5/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000278	PMID:38991538	PCS		6/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001249	PMID:38991538;PMID:39369315	PCS		48/48			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000710	PMID:38991538	PCS		0/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0020206	PMID:38991538	PCS		1/40			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000297	PMID:38991538;PMID:39369315	PCS		9/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001264	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001266	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000293	PMID:38859706;PMID:38991538	PCS		5/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011968	PMID:38991538;PMID:39369315	PCS		23/25			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001263	PMID:38991538;PMID:39369315	PCS		16/16			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000609	PMID:38991538	PCS		8/37			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001816	PMID:38859706;PMID:38991538;PMID:39369315	PCS		2/21			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000729	PMID:38991538;PMID:39369315	PCS		18/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000722	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000601	PMID:38991538;PMID:39369315	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001257	PMID:39369315	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0030799	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000385	PMID:38991538;PMID:39369315	PCS		12/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000023	PMID:39369315	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012368	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000939	PMID:39369315	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002317	PMID:38859706;PMID:38991538	PCS		6/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0009765	PMID:38991538	PCS		3/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000378	PMID:38991538	PCS		3/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000396	PMID:38991538	PCS		5/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000154	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0033715	PMID:38991538	PCS		0/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000276	PMID:38859706;PMID:38991538	PCS		5/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011825	PMID:38859706;PMID:38991538;PMID:39369315	PCS		21/52			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001483	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0045025	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0005280	PMID:38991538;PMID:39369315	PCS		10/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0034494	PMID:38991538	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000821	PMID:38991538	PCS		2/33			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0009739	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000483	PMID:39369315	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000365	PMID:38991538	PCS		9/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002540	PMID:38859706;PMID:38991538	PCS		6/37			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000486	PMID:38991538;PMID:39369315	PCS		32/56			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001332	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0003196	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0033725	PMID:38991538	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012471	PMID:38859706;PMID:38991538;PMID:39369315	PCS		14/21			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002539	PMID:38991538	PCS		0/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0040019	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000358	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000253	PMID:39369315	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000494	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000252	PMID:38991538	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001344	PMID:38859706;PMID:38991538;PMID:39369315	PCS		49/59			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000490	PMID:38859706;PMID:38991538;PMID:39369315	PCS		3/61			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0031432	PMID:39369315	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0034397	PMID:39369315	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002308	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001339	PMID:38991538	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002307	PMID:38991538;PMID:39369315	PCS		15/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001334	PMID:38991538	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000248	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000369	PMID:38991538;PMID:39369315	PCS		5/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000006	PMID:38991538	PCS					I	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000341	PMID:38991538;PMID:39369315	PCS		5/60			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000340	PMID:38859706;PMID:38991538	PCS		2/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000582	PMID:38859706;PMID:38991538	PCS		1/41			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000463	PMID:38991538	PCS		4/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000460	PMID:38859706;PMID:38991538	PCS		2/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000581	PMID:38859706;PMID:38991538;PMID:39369315	PCS		15/52			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012444	PMID:38991538	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012446	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0004938	PMID:39369315	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000219	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0007302	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000218	PMID:38991538;PMID:39369315	PCS		10/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000455	PMID:38859706;PMID:38991538;PMID:39369315	PCS		7/61			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000456	PMID:38991538;PMID:39369315	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000472	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002650	PMID:39369315	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000232	PMID:38991538	PCS		0/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000474	PMID:39369315	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0005487	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000592	PMID:38859706;PMID:38991538;PMID:39369315	PCS		9/61			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0005484	PMID:38991538	PCS		8/39			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0003186	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000470	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001680	PMID:39369315	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011344	PMID:38859706;PMID:38991538	PCS		35/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011228	PMID:38991538;PMID:39369315	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012683	PMID:38991538	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0034295	PMID:38991538	PCS		4/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0007651	PMID:38859706;PMID:38991538	PCS		8/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000348	PMID:38859706;PMID:38991538;PMID:39369315	PCS		5/61			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002527	PMID:38991538	PCS		0/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0007655	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001555	PMID:39369315	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000347	PMID:38859706;PMID:38991538	PCS		3/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0010804	PMID:38991538;PMID:39369315	PCS		11/20			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002188	PMID:38859706;PMID:38991538;PMID:39369315	PCS		4/57			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0010808	PMID:38859706;PMID:38991538	PCS		3/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0010806	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012429	PMID:39369315	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001090	PMID:38859706;PMID:38991538	PCS		3/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011343	PMID:38859706;PMID:38991538	PCS		10/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011342	PMID:38859706;PMID:38991538	PCS		0/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000319	PMID:38859706;PMID:38991538	PCS		2/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011461	PMID:38859706	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000316	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001763	PMID:39369315	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0005469	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000692	PMID:38859706;PMID:38991538	PCS		2/41			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002079	PMID:38991538;PMID:39369315	PCS		9/55			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000331	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002871	PMID:38859706	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002194	PMID:38991538	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0030822	PMID:38991538	PCS		0/40			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:4000079	PMID:38991538	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0011451	PMID:38991538	PCS		20/39			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001537	PMID:39369315	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0007874	PMID:38859706;PMID:38991538	PCS		4/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000322	PMID:38991538	PCS		4/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000325	PMID:38991538;PMID:39369315	PCS		8/51			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002500	PMID:38991538	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000324	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002169	PMID:38991538	PCS		3/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000540	PMID:39369315	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002283	PMID:38991538;PMID:39369315	PCS		1/56			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002282	PMID:38991538	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0410170	PMID:38991538	PCS		3/45			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002280	PMID:38859706;PMID:38991538	PCS		9/46			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0040080	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0012531	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001508	PMID:38991538;PMID:39369315	PCS		37/54			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001629	PMID:39369315	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000414	PMID:38859706;PMID:38991538	PCS		2/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002837	PMID:39369315	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002714	PMID:38859706;PMID:38991538	PCS		2/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0006532	PMID:39369315	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000411	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002059	PMID:38991538	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000431	PMID:38859706;PMID:38991538	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0031936	PMID:38859706;PMID:38991538	PCS		46/47			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000430	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0030048	PMID:39369315	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:6000029	PMID:38991538	PCS		2/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002292	PMID:38991538	PCS		1/49			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0002171	PMID:38859706;PMID:38991538	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000426	PMID:38859706;PMID:38991538	PCS		2/50			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0001511	PMID:38991538	PCS		17/44			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:620851	ReNU syndrome		HP:0000545	PMID:39369315	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0001320	OMIM:610992	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0001276	PMID:17436247	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0011968	PMID:17436247	PCS		1/2			P	HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0001250	OMIM:610992	TAS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0500228	PMID:17436247	PCS		2/2			P	HPO:probinson[2022-09-28];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0001263	OMIM:610992	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0005484	OMIM:610992	IEA					P	HPO:iea[2009-02-17]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0012279	PMID:17436247	PCS		2/2			P	HPO:probinson[2013-04-07];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0012277	PMID:17436247	PCS		2/2			P	HPO:probinson[2013-04-07];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0200048	PMID:17436247	PCS		1/2			P	HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0000007	PMID:17436247	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0001522	PMID:17436247	PCS		1/2			C	HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0002104	PMID:17436247	PCS		1/2			P	HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0001336	PMID:17436247	PCS		1/2			P	HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0003623	PMID:17436247	PCS		2/2			C	HPO:probinson[2022-09-28];HPO:probinson[2022-09-28]
OMIM:610992	Phosphoserine aminotransferase deficiency		HP:0034390	PMID:17436247	PCS		2/2			P	HPO:probinson[2022-10-06]
OMIM:100070	Aortic aneurysm, abdominal		HP:0005112	PMID:7613891	PCS	HP:0003581				P	HPO:probinson[2009-02-17]
OMIM:100070	Aortic aneurysm, abdominal		HP:0000007	OMIM:100070	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:100070	Aortic aneurysm, abdominal		HP:0001426	OMIM:100070	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:100070	Aortic aneurysm, abdominal		HP:0000006	OMIM:100070	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:156550	Kniest dysplasia		HP:0002663	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0003037	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0003015	OMIM:156550	TAS					P	HPO:probinson[2012-05-26]
OMIM:156550	Kniest dysplasia		HP:0002982	PMID:7874117	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0003577	PMID:7874117	PCS		1/1			C	HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0000541	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0008905	PMID:7874117	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0000023	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0001376	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0003273	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0001270	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0008271	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0006172	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000518	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0006375	PMID:7874117	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0004619	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0200003	OMIM:156550	TAS					P	HPO:probinson[2012-05-26]
OMIM:156550	Kniest dysplasia		HP:0002812	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0002779	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000311	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0003521	OMIM:156550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:156550	Kniest dysplasia		HP:0000175	PMID:7874117	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0008839	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0001288	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0002970	PMID:7874117	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0002098	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000272	PMID:7874117	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0000470	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0011800	OMIM:156550	TAS					P	HPO:skoehler[2015-11-15]
OMIM:156550	Kniest dysplasia		HP:0005280	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000947	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0002827	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000926	PMID:7874117	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0000767	PMID:7874117	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0001537	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000403	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0003417	PMID:7874117	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:156550	Kniest dysplasia		HP:0000405	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000520	OMIM:156550	IEA					P	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000006	OMIM:156550	IEA					I	HPO:iea[2009-02-17]
OMIM:156550	Kniest dysplasia		HP:0000545	PMID:7874117	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:121900	Groenouw type I corneal dystrophy		HP:0007802	OMIM:121900	IEA					P	HPO:iea[2009-02-17]
OMIM:121900	Groenouw type I corneal dystrophy		HP:0000486	OMIM:121900	IEA					P	HPO:iea[2009-02-17]
OMIM:121900	Groenouw type I corneal dystrophy		HP:0007827	OMIM:121900	IEA					P	HPO:iea[2009-02-17]
OMIM:121900	Groenouw type I corneal dystrophy		HP:0000518	OMIM:121900	IEA					P	HPO:iea[2009-02-17]
OMIM:121900	Groenouw type I corneal dystrophy		HP:0007809	OMIM:121900	IEA					P	HPO:iea[2009-02-17]
OMIM:121900	Groenouw type I corneal dystrophy		HP:0000006	PMID:9054935	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-27]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000154	PMID:31031012	PCS		6/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0002069	PMID:31031012	PCS		1/9			P	HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0002136	PMID:31031012	PCS		2/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000252	PMID:31031012	PCS		2/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0001792	PMID:31031012	PCS		2/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0001344	PMID:31031012	PCS		8/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0002540	PMID:31031012	PCS		5/9			P	HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0002079	PMID:31031012	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0002283	PMID:31031012	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0001252	PMID:31031012	PCS		5/6			P	HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0003593	PMID:31031012	PCS		10/10			C	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0011344	PMID:31031012	PCS		10/10			P	HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0012469	PMID:31031012	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0011220	PMID:31031012	PCS		4/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000729	PMID:31031012	PCS		3/5			P	HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0009882	PMID:31031012	PCS		4/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000316	PMID:31031012	PCS		6/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000337	PMID:31031012	PCS		4/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000414	PMID:31031012	PCS		10/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000006	PMID:31031012	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:618470	Intellectual developmental disorder with severe speech and ambulation defects		HP:0000699	PMID:31031012	PCS		1/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-09]
OMIM:617743	Oocyte maturation defect 4		HP:0008222	PMID:28965844	PCS		4/4			P	HPO:probinson[2022-10-01]
OMIM:617743	Oocyte maturation defect 4		HP:0011462	PMID:28965844	PCS		4/4			C	HPO:probinson[2022-10-01]
OMIM:617743	Oocyte maturation defect 4		HP:0000007	PMID:28965844	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000365	PMID:22077973	PCS		9/19			P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000581	PMID:22077973	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0001252	PMID:22077973	PCS		16/19			P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0003593	PMID:22077973	PCS		19/19			C	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0001270	PMID:22077973	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000414	PMID:22077973	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0001847	PMID:22077973	PCS		10/19			P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000219	PMID:22077973	PCS					P	HPO:probinson[2023-01-23];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0002999	PMID:22077973	PCS					P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000537	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000358	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0001644	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000252	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000175	PMID:22077973	PCS		6/19			P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0011968	PMID:22077973	PCS		18/19			P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000691	PMID:22077973	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0005280	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0032524	PMID:22077973	PCS		10/19			P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000821	PMID:22077973	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000047	PMID:22077973	PCS		4/10			P	HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000006	PMID:22077973	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000028	PMID:22077973	PCS		8/9	MALE		P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000369	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000347	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603736	Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant		HP:0000269	OMIM:603736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000286	PMID:25792360	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002389	PMID:25792360	PCS		2/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0010804	OMIM:616449	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000486	PMID:25792360	PCS		1/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001250	PMID:25792360	PCS		3/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001252	PMID:25792360	PCS		4/5			P	HPO:skoehler[2015-07-26]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000482	PMID:25792360	PCS		2/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002020	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0003593	PMID:25792360	PCS		2/6			C	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000518	PMID:25792360	PCS		4/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0008499	PMID:25792360	PCS		1/6			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000316	PMID:25792360	PCS		2/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000954	PMID:25792360	PCS		2/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002019	PMID:25792360	PCS		2/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000278	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000175	PMID:25792360	PCS		2/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000494	PMID:25792360	PCS		3/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000252	OMIM:616449	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002079	PMID:25792360	PCS		3/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001263	PMID:25792360	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0004691	PMID:25792360	PCS		3/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000007	PMID:25792360	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000568	PMID:25792360	PCS		1/6			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000768	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000047	PMID:25792360	PCS		4/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000322	PMID:25792360	PCS		3/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001257	OMIM:616449	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000369	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000126	OMIM:616449	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0003577	PMID:25792360	PCS		4/6			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000463	PMID:25792360	PCS		2/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000221	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000023	PMID:25792360	PCS		1/6			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001274	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0008070	PMID:25792360	PCS		5/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001629	PMID:25792360	PCS		1/6			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002119	PMID:25792360	PCS		2/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000218	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0006532	PMID:25792360	PCS		2/6			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002059	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002650	PMID:25792360	PCS		1/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000232	OMIM:616449	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0009909	PMID:25792360	PCS		1/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002092	PMID:25792360	PCS		1/6			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002808	PMID:25792360	PCS		1/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000508	PMID:25792360	PCS		4/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0008665	PMID:25792360	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0007413	PMID:25792360	PCS		5/5			P	HPO:probinson[2023-03-04]
OMIM:616449	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001631	PMID:25792360	PCS		2/6			P	HPO:probinson[2023-03-04]
OMIM:618464	Paragangliomas 6		HP:0003334	PMID:29431636	IEA					P	HPO:probinson[2019-07-06]
OMIM:618464	Paragangliomas 6		HP:0000822	PMID:29431636	PCS					P	HPO:probinson[2019-07-06]
OMIM:618464	Paragangliomas 6		HP:0002668	PMID:29431636	PCS	HP:0003581	7/7			P	HPO:probinson[2019-07-06]
OMIM:618464	Paragangliomas 6		HP:0000006	PMID:29431636	PCS					I	HPO:probinson[2019-07-06];HPO:probinson[2019-07-06]
OMIM:617757	Joubert syndrome 32		HP:0000098	PMID:28965847	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0003577	PMID:28965847	PCS		4/4			C	HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001520	PMID:28965847	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001162	PMID:28965847	PCS		3/4			P	HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001260	OMIM:617757	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617757	Joubert syndrome 32		HP:0001263	PMID:28965847	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001252	PMID:28965847	PCS		3/4			P	HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001251	PMID:28965847	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0002280	PMID:28965847	PCS		1/2			P	HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0005280	PMID:28965847	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0000639	PMID:28965847	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001639	PMID:28965847	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001317	OMIM:617757	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617757	Joubert syndrome 32		HP:0000316	PMID:28965847	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0000657	PMID:28965847	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0000007	PMID:28965847	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0002419	PMID:28965847	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0002007	PMID:28965847	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0001830	PMID:28965847	PCS		2/4			P	HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0000256	PMID:28965847	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617757	Joubert syndrome 32		HP:0002126	PMID:28965847	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000252	PMID:30289604	PCS	HP:0003577	3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000431	PMID:21937992	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000750	PMID:30289604;PMID:26308914	PCS		4/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0031936	PMID:26308914	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001250	PMID:30289604	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001272	PMID:30289604	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001252	PMID:30289604	PCS		1/4			P	HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001263	PMID:21937992	PCS		3/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0003593	PMID:26308914	PCS		3/3			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0045025	PMID:26308914	PCS		2/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001270	PMID:30289604	PCS		1/4			P	HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0011229	PMID:26308914	PCS		2/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001518	PMID:30289604;PMID:26308914	PCS		3/7			P	HPO:probinson[2022-03-11];HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000327	PMID:26308914	PCS		3/5			P	HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0006970	PMID:30289604	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000238	PMID:30289604	PCS		1/4			P	HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000007	PMID:21937992	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000664	PMID:21937992	PCS		3/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0000411	PMID:26308914	PCS		2/5			P	HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001324	PMID:30289604	PCS		1/4			P	HPO:probinson[2022-03-11]
OMIM:618302	Intellectual developmental disorder, autosomal recessive 68		HP:0001763	PMID:30289604	PCS	HP:0003621	2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000044	PMID:20507343	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0008209	PMID:20507343	PCS		1/4	FEMALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000365	PMID:20507343	PCS		4/7			P	HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0001596	PMID:20507343	PCS		7/7			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0001332	PMID:20507343	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0005135	OMIM:241080	PCS					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0003077	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0030353	OMIM:241080	TAS					P	HPO:skoehler[2015-12-30]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0008070	OMIM:241080	PCS					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000819	PMID:20507343	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000738	OMIM:241080	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000815	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0008697	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0008734	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000411	OMIM:241080	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000674	OMIM:241080	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0001249	PMID:20507343	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0002213	OMIM:241080	PCS					P	HPO:iea[2012-03-01]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000054	PMID:20507343	PCS		1/3	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000013	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0001266	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0001260	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0040171	OMIM:241080	TAS					P	HPO:skoehler[2015-08-05]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0002071	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000709	OMIM:241080	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000407	OMIM:241080	PCS					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000426	OMIM:241080	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000007	PMID:19026396	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0002925	OMIM:241080	IEA					P	HPO:iea[2009-02-17]
OMIM:241080	Woodhouse-Sakati syndrome		HP:0000325	OMIM:241080	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609227	Griscelli syndrome, type 3		HP:0011463	PMID:12897212	PCS		2/2			C	HPO:probinson[2022-06-23]
OMIM:609227	Griscelli syndrome, type 3		HP:0000707	PMID:12897212	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-23]
OMIM:609227	Griscelli syndrome, type 3		HP:0000007	PMID:12897212	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-06-23]
OMIM:609227	Griscelli syndrome, type 3		HP:0002218	PMID:12897212	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-06-23]
OMIM:609227	Griscelli syndrome, type 3		HP:0004527	PMID:12897212	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-06-23]
OMIM:609227	Griscelli syndrome, type 3		HP:0002227	PMID:12897212	PCS		2/2			P	HPO:probinson[2013-12-17];HPO:probinson[2022-06-23]
OMIM:609227	Griscelli syndrome, type 3		HP:0002721	PMID:12897212	PCS		0/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-23]
OMIM:616307	Senior-Loken syndrome 8		HP:0003774	PMID:23559409	PCS		4/4			P	HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0003621	PMID:25726036	PCS		1/2			C	HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0000980	OMIM:616307	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616307	Senior-Loken syndrome 8		HP:0000090	PMID:23559409	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0033149	PMID:25726036;PMID:23559409	PCS		4/6			P	HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0010442	PMID:23559409	PCS		1/4			P	HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0033601	PMID:25726036	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0011463	PMID:25726036	PCS		1/2			C	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0007663	OMIM:616307	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616307	Senior-Loken syndrome 8		HP:0000007	PMID:23559409	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0002617	OMIM:616307	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616307	Senior-Loken syndrome 8		HP:0001407	PMID:23559409	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0001737	PMID:23559409	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0000505	OMIM:616307	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616307	Senior-Loken syndrome 8		HP:0007401	OMIM:616307	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616307	Senior-Loken syndrome 8		HP:0004737	PMID:25726036	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0000510	PMID:25726036	PCS		2/2			P	HPO:probinson[2022-07-19]
OMIM:616307	Senior-Loken syndrome 8		HP:0000556	PMID:23559409	PCS		1/4			P	HPO:probinson[2022-07-19]
OMIM:229300	Friedreich ataxia 1		HP:0003115	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0003232	OMIM:229300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:229300	Friedreich ataxia 1		HP:0002066	OMIM:229300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:229300	Friedreich ataxia 1		HP:0001251	OMIM:229300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:229300	Friedreich ataxia 1		HP:0000819	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0000639	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0007663	OMIM:229300	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:229300	Friedreich ataxia 1		HP:0003209	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0001626	OMIM:229300	TAS					P	HPO:skoehler[2014-03-24]
OMIM:229300	Friedreich ataxia 1		HP:0003448	PMID:6231891	PCS					P	HPO:probinson[2012-04-18]
OMIM:229300	Friedreich ataxia 1		HP:0003621	OMIM:229300	IEA					C	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0002650	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0001761	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0003487	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0001123	OMIM:229300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:229300	Friedreich ataxia 1		HP:0001260	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0002495	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0002070	OMIM:229300	TAS					P	HPO:skoehler[2012-11-22]
OMIM:229300	Friedreich ataxia 1		HP:0010831	OMIM:229300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:229300	Friedreich ataxia 1		HP:0001639	OMIM:229300	TAS					P	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0000649	OMIM:229300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:229300	Friedreich ataxia 1		HP:0007078	PMID:6231891	PCS					P	HPO:probinson[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0000007	OMIM:229300	IEA					I	HPO:iea[2009-02-17]
OMIM:229300	Friedreich ataxia 1		HP:0001635	OMIM:229300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:229300	Friedreich ataxia 1		HP:0000648	OMIM:229300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:229300	Friedreich ataxia 1		HP:0000505	OMIM:229300	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:229300	Friedreich ataxia 1		HP:0000763	OMIM:229300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:229300	Friedreich ataxia 1		HP:0002522	OMIM:229300	IEA					P	HPO:iea[2009-02-17]
DECIPHER:14	Prader-Willi syndrome (Type 1)		HP:0001252	DECIPHER:14	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:14	Prader-Willi syndrome (Type 1)		HP:0008872	DECIPHER:14	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:14	Prader-Willi syndrome (Type 1)		HP:0001956	DECIPHER:14	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:14	Prader-Willi syndrome (Type 1)		HP:0000135	DECIPHER:14	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:14	Prader-Willi syndrome (Type 1)		HP:0001249	DECIPHER:14	IEA					P	HPO:skoehler[2013-05-29]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0003621	PMID:25691535	PCS		2/2			C	HPO:probinson[2021-06-26]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0032705	PMID:25691535	PCS		1/2			P	HPO:probinson[2021-06-26]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0002384	OMIM:616461	TAS					P	HPO:skoehler[2015-08-02]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0002384	PMID:25691535	PCS	HP:0011462	2/2			P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0007334	PMID:25691535	PCS		2/2			P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0032785	PMID:25691535	PCS		1/2			P	HPO:probinson[2021-06-26]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0032864	PMID:25691535	PCS		1/2			P	HPO:probinson[2021-06-26]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0012005	PMID:25691535	PCS		2/2			P	HPO:probinson[2021-06-26]
OMIM:616461	Epilepsy, familial temporal lobe, 8		HP:0000006	PMID:25691535	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-26]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0003212	PMID:32207811	PCS		11/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002780	PMID:32207811	PCS		1/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0003593	PMID:32207811	PCS		2/11			C	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0032434	PMID:32207811	PCS		1/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0031292	PMID:32207811	PCS		4/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0011463	PMID:32207811	PCS		8/11			C	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0001888	PMID:32207811	PCS		1/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0006532	PMID:32207811	PCS		10/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0000218	PMID:32207811	PCS		3/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002659	PMID:32207811	PCS		4/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0006335	PMID:32207811	PCS		9/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0025419	PMID:32207811	PCS		6/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0004315	PMID:32207811	PCS		2/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0040218	PMID:32207811	PCS		2/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002850	PMID:32207811	PCS		2/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0003621	PMID:32207811	PCS		1/11			C	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0001047	PMID:32207811	PCS		8/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002650	PMID:32207811	PCS		6/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0001762	PMID:32207811	PCS		2/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0001382	PMID:32207811	PCS		7/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002099	PMID:32207811	PCS		8/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002110	PMID:32207811	PCS		6/10			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0001581	PMID:32207811	PCS		4/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0011069	PMID:32207811	PCS		3/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002728	PMID:32207811	PCS		1/11			P	HPO:probinson[2022-04-03];HPO:probinson[2022-07-10]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0500093	PMID:32207811	PCS		1/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002788	PMID:32207811	PCS		6/11			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0000006	PMID:32207811	PCS					I	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0002720	PMID:32207811	PCS		4/12			P	HPO:probinson[2022-04-03]
OMIM:619752	Hyper-IgE recurrent infection syndrome 4A, autosomal dominant		HP:0001875	PMID:32207811	PCS		1/12			P	HPO:probinson[2022-04-03]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0002267	PMID:15852396	PCS		22/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0003676	PMID:15852396	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0002650	PMID:15852396	PCS		14/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0002540	PMID:15852396	PCS		3/22			P	HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0001761	OMIM:609541	IEA					P	HPO:iea[2009-02-17]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0003487	PMID:15852396	PCS		2/22			P	HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0001371	PMID:15852396	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0003693	PMID:15852396	PCS	HP:0011462	19/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0001260	PMID:15852396	PCS	HP:0011462	19/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0003593	PMID:15852396	PCS		17/18			C	HPO:probinson[2022-02-15];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0003390	PMID:15852396	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0001270	PMID:15852396	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0011448	PMID:15852396	PCS		8/22			P	HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0000639	PMID:15852396	PCS		17/22			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0002808	PMID:15852396	PCS		14/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0007054	PMID:15852396	PCS		19/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0011463	PMID:15852396	PCS		1/18			C	HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0007002	PMID:15852396	PCS					P	HPO:iea[2012-03-12];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0000975	PMID:15852396	PCS		16/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0000007	PMID:26385635	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0000648	PMID:15852396	PCS		21/22			P	HPO:probinson[2012-04-07];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0001258	PMID:15852396	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0000543	PMID:15852396	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-15]
OMIM:609541	Spastic paraplegia, optic atrophy, and neuropathy		HP:0003438	PMID:15852396	PCS		14/22			P	HPO:probinson[2022-02-15]
OMIM:607578	Breath-Holding spells		HP:0000708	OMIM:607578	IEA					P	HPO:iea[2009-02-17]
OMIM:607578	Breath-Holding spells		HP:0001891	OMIM:607578	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607578	Breath-Holding spells		HP:0000980	OMIM:607578	TAS					P	HPO:iea[2009-02-17]
OMIM:607578	Breath-Holding spells		HP:0007185	OMIM:607578	IEA					P	HPO:iea[2009-02-17]
OMIM:607578	Breath-Holding spells		HP:0000961	OMIM:607578	TAS					P	HPO:iea[2009-02-17]
OMIM:607578	Breath-Holding spells		HP:0000006	OMIM:607578	IEA					I	HPO:iea[2009-02-17]
OMIM:618458	Knobloch syndrome 2		HP:0000541	PMID:33693784	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0001250	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0001195	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0002021	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0001263	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0033542	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0002084	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0011003	PMID:33693784	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0100832	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0012450	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0000717	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0006297	PMID:33693784	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0006530	PMID:33693784	PCS		2/2			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0007795	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0007773	PMID:33693784	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0002205	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0001643	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0000006	PMID:33693784	PCS					I	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0001249	PMID:33693784	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:618458	Knobloch syndrome 2		HP:0000347	PMID:33693784	PCS		2/2		HP:0012825	P	HPO:probinson[2022-08-20]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0025331	PMID:26633546	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0005743	PMID:26633546	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0003577	PMID:26633546	PCS		3/3			C	HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0001047	OMIM:614262	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0002021	PMID:26633546	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0000293	OMIM:614262	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0002099	PMID:26633546	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0012385	PMID:26633546	PCS		2/3			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0001629	PMID:26633546	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0001845	PMID:26633546	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0000007	PMID:26633546	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0002804	PMID:26633546	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0001631	PMID:26633546	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:614262	Arthrogryposis, perthes disease, and upward gaze palsy		HP:0001642	PMID:26633546	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0003550	OMIM:153400	TAS					P	HPO:probinson[2009-02-17]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0012804	OMIM:153400	TAS					P	HPO:skoehler[2015-01-20]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0003011	OMIM:153400	IEA					P	HPO:iea[2009-02-17]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0001790	PMID:11078474	PCS		2/43			P	HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0011675	OMIM:153400	IEA					P	HPO:iea[2009-02-17]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0001629	PMID:15523639	PCS		1/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0002619	OMIM:153400	TAS					P	HPO:probinson[2009-02-17]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000613	PMID:15523639;PMID:11078474	PCS		10/49			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000656	PMID:11078474	PCS		2/43			P	HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0009743	PMID:15523639;PMID:11078474	PCS		42/42			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0001643	OMIM:153400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0001004	PMID:15523639	PCS	HP:0003621				P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000476	PMID:11078474	PCS		2/43			P	HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000495	OMIM:153400	IEA					P	HPO:iea[2009-02-17]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000175	PMID:11078474	PCS		5/39			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0011367	OMIM:153400	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0010310	PMID:15523639	PCS		1/6			P	HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0002808	PMID:15523639	PCS		2/5			P	HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000509	OMIM:153400	TAS					P	HPO:iea[2009-02-17]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000508	PMID:11078474	PCS		2/39			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0100658	PMID:15523639	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0001636	PMID:11078474	PCS	HP:0003577	3/39			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000568	PMID:15523639	PCS		1/6			P	HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000465	PMID:11078474	PCS		6/43			P	HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000204	OMIM:153400	IEA					P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000006	PMID:11078474	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:153400	Lymphedema-Distichiasis syndrome		HP:0000347	PMID:15523639	PCS		2/5			P	HPO:probinson[2022-11-02]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0002212	PMID:17273967;PMID:18445049	PCS		4/4			P	HPO:probinson[2022-04-17];HPO:skoehler[2014-05-04];HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0007957	PMID:17273967	PCS		1/3			P	HPO:skoehler[2014-05-04]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0003577	PMID:17273967;PMID:18445049	PCS		4/4			C	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0001597	PMID:18445049	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-10]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0002299	PMID:17273967	PCS		3/3			P	HPO:skoehler[2015-08-16]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0002231	PMID:18445049	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0045075	PMID:17273967;PMID:18445049	PCS		4/4			P	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0008070	PMID:17273967;PMID:18445049	PCS		4/4			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0000613	PMID:17273967;PMID:18445049	PCS		3/4			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-04-17];HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0007431	PMID:17273967	PCS	HP:0003577	3/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0007431	PMID:18445049	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0000007	PMID:18445049	PCS					I	HPO:skoehler[2014-05-04]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0000989	PMID:17273967	PCS		3/3			P	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0000966	PMID:17273967	PCS		0/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0007665	PMID:17273967	PCS		3/3			P	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0000653	PMID:18445049	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0011082	PMID:17273967	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0000498	PMID:18445049	PCS		1/1			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0003777	PMID:17273967	PCS		3/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-04-17]
OMIM:602400	Ichthyosis, congenital, autosomal recessive 11		HP:0000962	OMIM:602400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:105120	Amyloidosis, Finnish type		HP:0030843	PMID:7836945	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0003774	PMID:8395367	PCS		2/2			P	HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0001278	PMID:7836945	PCS		9/28			P	HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0000100	PMID:8395367	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0001283	OMIM:105120	IEA					P	HPO:iea[2009-02-17]
OMIM:105120	Amyloidosis, Finnish type		HP:0001271	OMIM:105120	IEA					P	HPO:iea[2009-02-17]
OMIM:105120	Amyloidosis, Finnish type		HP:0000083	OMIM:105120	IEA					P	HPO:iea[2009-02-17]
OMIM:105120	Amyloidosis, Finnish type		HP:0003581	PMID:33499149	PCS		7/7			C	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0034368	PMID:33499149	PCS		2/7			P	HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0031861	PMID:7836945	PCS					P	HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0032614	PMID:8395367	PCS		2/2			P	HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0000518	PMID:33499149	PCS		2/7			P	HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0001638	PMID:33499149	PCS		1/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0000006	PMID:8395367	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0000973	PMID:33499149	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0003216	OMIM:105120	IEA					P	HPO:iea[2009-02-17]
OMIM:105120	Amyloidosis, Finnish type		HP:0001149	PMID:33499149	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:105120	Amyloidosis, Finnish type		HP:0001138	PMID:33499149	PCS		1/7			P	HPO:probinson[2024-03-06]
OMIM:604717	Deafness, autosomal dominant 20		HP:0008619	OMIM:604717	TAS					P	HPO:probinson[2009-02-17]
OMIM:604717	Deafness, autosomal dominant 20		HP:0000408	OMIM:604717	TAS					P	HPO:probinson[2009-02-17]
OMIM:604717	Deafness, autosomal dominant 20		HP:0011462	OMIM:604717	TAS					C	HPO:probinson[2012-07-16]
OMIM:604717	Deafness, autosomal dominant 20		HP:0000006	PMID:13680526	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-13]
OMIM:614504	Usher syndrome, type IIIB		HP:0007083	PMID:22279524	PCS		3/3			P	HPO:probinson[2023-05-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0000365	PMID:22279524	PCS		3/3			P	HPO:skoehler[2013-01-22]
OMIM:614504	Usher syndrome, type IIIB		HP:0002078	PMID:22279524	PCS		3/3		HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:614504	Usher syndrome, type IIIB		HP:0011463	PMID:22279524	PCS		3/3			C	HPO:probinson[2023-05-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0000613	PMID:22279524	PCS		3/3			P	HPO:skoehler[2012-10-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0000007	PMID:22279524	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0002194	PMID:22279524	PCS		3/3			P	HPO:skoehler[2012-10-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0000505	PMID:22279524	PCS		3/3			P	HPO:skoehler[2013-01-22]
OMIM:614504	Usher syndrome, type IIIB		HP:0000543	PMID:22279524	PCS		3/3			P	HPO:skoehler[2012-10-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0007843	PMID:22279524	PCS		3/3			P	HPO:probinson[2023-05-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0011504	PMID:22279524	PCS		3/3			P	HPO:probinson[2023-05-17]
OMIM:614504	Usher syndrome, type IIIB		HP:0000666	PMID:22279524	PCS		3/3			P	HPO:skoehler[2013-01-22]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0002421	PMID:8651643	PCS	HP:0003593	1/1			P	HPO:probinson[2022-10-18];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0010628	OMIM:616313	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003577	OMIM:616313	TAS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003555	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003198	PMID:8651643	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0001371	PMID:8651643	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003473	PMID:8872460	PCS	HP:0003577	1/1			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0001252	OMIM:616313	TAS	HP:0003623				P	HPO:skoehler[2015-05-31]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003690	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0000218	PMID:8651643	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0025336	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003803	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0001620	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003403	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003202	PMID:8651643	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0000275	OMIM:616313	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0000276	PMID:8651643	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003388	PMID:8651643	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0031936	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0002033	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0030208	PMID:8872460;PMID:8651643	PCS		0/2			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0006380	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0000508	PMID:8651643	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0000602	PMID:8651643	PCS	HP:0003621	1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0001319	OMIM:616313	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0000006	PMID:8872460	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-18]
OMIM:616313	Myasthenic syndrome, congenital, 2A, slow-channel		HP:0003557	PMID:8651643	PCS		1/1			P	HPO:probinson[2022-10-18]
OMIM:615785	White sponge nevus 2		HP:0000969	OMIM:615785	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615785	White sponge nevus 2		HP:0025092	OMIM:615785	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615785	White sponge nevus 2		HP:0000006	OMIM:615785	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615785	White sponge nevus 2		HP:0040009	OMIM:615785	TAS					P	HPO:skoehler[2014-11-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0009926	PMID:25676728	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0003621	PMID:25676728	PCS					C	HPO:probinson[2023-01-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0011463	PMID:25676728	PCS					C	HPO:probinson[2023-01-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0000613	PMID:25676728	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0200026	PMID:25676728	PCS					P	HPO:probinson[2023-01-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0000505	PMID:25676728	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0000006	PMID:25676728	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:122400	Epithelial recurrent erosion dystrophy		HP:0200020	PMID:25676728	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2023-01-26]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003236	PMID:19085932	PCS		3/3			P	HPO:skoehler[2010-06-20]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0010628	OMIM:612954	TAS					P	HPO:skoehler[2014-08-03]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003691	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0002460	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0011463	PMID:19085932	PCS		1/3			C	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0007340	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0032341	PMID:19085932	PCS		1/3			P	HPO:skoehler[2019-04-18]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0002936	OMIM:612954	TAS					P	HPO:skoehler[2014-08-03]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0001723	PMID:19085932	PCS		2/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0006597	PMID:19085932	PCS		1/3			P	HPO:skoehler[2010-06-19]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003327	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003701	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003306	PMID:19085932	PCS		2/3			P	HPO:skoehler[2012-10-17]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003447	OMIM:612954	TAS					P	HPO:skoehler[2014-08-03]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0007108	PMID:19085932	PCS		1/3			P	HPO:skoehler[2010-06-20]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003700	OMIM:612954	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0001265	OMIM:612954	TAS					P	HPO:skoehler[2014-08-03]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003324	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003621	PMID:19085932	PCS		2/3			C	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0002650	PMID:19085932	PCS		1/3			P	HPO:skoehler[2010-06-19]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003388	PMID:19085932	PCS		1/3			P	HPO:skoehler[2010-06-19]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0001761	OMIM:612954	TAS					P	HPO:skoehler[2014-08-03]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003560	OMIM:612954	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0002093	PMID:19085932	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0002091	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0008081	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0006380	OMIM:612954	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0001639	PMID:19085932	PCS		1/3			P	HPO:skoehler[2010-06-19]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003715	OMIM:612954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0030051	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0001653	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0002943	PMID:19085932	PCS		1/3			P	HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0000006	PMID:19085932	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003458	PMID:19085932	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-28]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0001611	PMID:19085932	PCS		1/3			P	HPO:skoehler[2010-06-19]
OMIM:612954	Myopathy, myofibrillar, 6		HP:0003678	OMIM:612954	IEA					C	HPO:skoehler[2010-06-19]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0003233	PMID:2506176	PCS					P	HPO:probinson[2022-10-03]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0003146	PMID:2506176	PCS					P	HPO:probinson[2022-10-03]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0001084	PMID:2506176	PCS					P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0011462	PMID:2506176	PCS					C	HPO:probinson[2022-10-03]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0012153	PMID:2506176	PCS					P	HPO:probinson[2022-10-03]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0005181	PMID:2506176	PCS					P	HPO:probinson[2022-10-03]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0000006	PMID:2506176	PCS					I	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620058	Familial apolipoprotein gene cluster deletion syndrome		HP:0031799	PMID:2506176	PCS					P	HPO:probinson[2022-10-03]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0004322	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0001260	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0001419	OMIM:300619	IEA					I	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0001252	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0001251	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0002174	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0001290	OMIM:300619	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0001324	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0007787	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:300619	Cataract, ataxia, short stature, and impaired intellectual development		HP:0001249	OMIM:300619	IEA					P	HPO:iea[2009-02-17]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001374	PMID:19576563;PMID:21487760	PCS		6/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0010648	PMID:21487760	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0003199	PMID:19576563	PCS		1/3			P	HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0002020	PMID:19576563	PCS		1/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0011220	OMIM:612940	TAS		5/5			P	HPO:skoehler[2013-08-11];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000316	PMID:19576563	PCS		2/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000239	PMID:19576563	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000238	PMID:19576563	PCS		2/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001763	PMID:21487760	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001249	PMID:21487760	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000494	PMID:19576563	PCS		2/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000252	PMID:19576563	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001382	PMID:21487760	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000490	PMID:19576563;PMID:21487760	PCS		4/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-10];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001263	PMID:19576563	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000691	PMID:21487760	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001582	OMIM:612940	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0011800	PMID:19576563	PCS		3/4			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0007392	PMID:19576563;PMID:21487760	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-06-28];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0034197	PMID:19576563	PCS		5/5			C	HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0034273	PMID:19576563	PCS		5/5			P	HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000767	PMID:19576563;PMID:21487760	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-06-28];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000007	PMID:19576563	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000601	OMIM:612940	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001015	PMID:19576563	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000369	PMID:21487760	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000963	PMID:21487760	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000325	PMID:19576563;PMID:21487760	PCS		6/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000343	PMID:19576563	PCS		1/3			P	HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000023	PMID:19576563	PCS		1/3			P	HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001274	PMID:19576563	PCS		2/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000460	PMID:21487760	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001270	PMID:21487760	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001508	PMID:19576563	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000418	PMID:19576563	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000938	OMIM:612940	TAS					P	HPO:skoehler[2013-05-03]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000337	PMID:19576563	PCS		5/5			P	HPO:skoehler[2013-08-11];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000414	PMID:19576563	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001822	PMID:21487760	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000978	PMID:19576563	PCS		2/2			P	HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000218	PMID:19576563;PMID:21487760	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-28];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000411	PMID:19576563	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000973	PMID:21487760	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0002650	PMID:19576563	PCS		2/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001762	PMID:21487760	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000592	PMID:19576563;PMID:21487760	PCS		5/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0000272	OMIM:612940	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0100679	PMID:19576563	PCS		5/5			P	HPO:probinson[2022-08-10]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0004948	PMID:19576563	PCS		0/5			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-16]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0006487	OMIM:612940	TAS					P	HPO:skoehler[2013-05-03]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0002007	OMIM:612940	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0001511	PMID:19576563;PMID:21487760	PCS		11/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-10];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:612940	Cutis laxa, autosomal recessive, type IIB		HP:0002645	PMID:19576563	PCS		1/2			P	HPO:probinson[2022-08-10]
OMIM:134510	Factor VIII and factor IX, combined deficiency of		HP:0003125	OMIM:134510	TAS					P	HPO:probinson[2012-05-26]
OMIM:134510	Factor VIII and factor IX, combined deficiency of		HP:0011858	OMIM:134510	TAS					P	HPO:probinson[2012-05-26]
OMIM:134510	Factor VIII and factor IX, combined deficiency of		HP:0000006	OMIM:134510	TAS					I	HPO:probinson[2009-02-17]
OMIM:612798	Question mark ears, isolated		HP:0000364	PMID:23315542	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-30]
OMIM:612798	Question mark ears, isolated		HP:0030022	PMID:23315542	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-01-30]
OMIM:612798	Question mark ears, isolated		HP:0000006	PMID:23315542	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-30]
OMIM:605582	Cardiomyopathy, dilated, 1K		HP:0003581	PMID:11085912	PCS					C	HPO:probinson[2022-07-04]
OMIM:605582	Cardiomyopathy, dilated, 1K		HP:0033113	PMID:11085912	PCS		3/9			P	HPO:probinson[2022-07-04]
OMIM:605582	Cardiomyopathy, dilated, 1K		HP:0001635	PMID:11085912	IEA		5/9			P	HPO:probinson[2022-07-04]
OMIM:605582	Cardiomyopathy, dilated, 1K		HP:0000006	PMID:11085912	PCS					I	HPO:probinson[2022-07-04]
OMIM:605582	Cardiomyopathy, dilated, 1K		HP:0001644	PMID:11085912	PCS					P	HPO:probinson[2022-07-04]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001298	PMID:27122014	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0000486	PMID:27616477	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001250	PMID:27616477	PCS		3/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0012706	PMID:27616477	PCS		1/1			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002063	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001252	PMID:27616477	PCS		7/12			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002283	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0003593	PMID:27122014;PMID:27616477	PCS		6/11			C	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001251	PMID:27616477	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0032794	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0030915	PMID:27616477	PCS		8/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002181	PMID:27616477	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0012444	PMID:27616477	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0000639	PMID:27616477	PCS		7/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0000737	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0011463	PMID:27616477	PCS		5/6			C	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0000711	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002119	PMID:27616477	PCS		3/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002878	PMID:27122014	PCS	HP:0011463	5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002318	PMID:27616477	PCS		2/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0006897	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0000511	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0200041	PMID:27616477	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0003128	PMID:27616477	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0000473	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002376	PMID:27122014;PMID:27616477	PCS		6/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002352	PMID:27616477	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001260	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002151	PMID:27616477	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001263	PMID:27616477	PCS					P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002273	PMID:27616477	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002196	PMID:27616477	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0002490	PMID:27616477	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0011922	PMID:27122014	PCS		0/5			P	HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0012378	PMID:27616477	PCS		1/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0012762	PMID:27616477	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0003819	PMID:27122014;PMID:27616477	PCS		10/11			C	HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0000007	PMID:27122014	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001337	PMID:27616477	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0003678	PMID:27122014	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0001259	PMID:27616477	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:617186	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1		HP:0046507	PMID:27616477	PCS		2/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:616298	Singleton-Merten syndrome 2		HP:0001650	PMID:25620203	PCS		1/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0000164	PMID:25620203	PCS		0/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0003621	PMID:25620203	PCS		4/11			C	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0002650	PMID:25620203	PCS		0/11			P	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0004322	PMID:25620203	PCS		2/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0011675	PMID:25620203	PCS		0/11			P	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0004380	PMID:25620203	PCS		5/7			P	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0009771	PMID:25620203	PCS		8/8			P	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0032153	PMID:25620203	PCS		1/11			P	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0011463	PMID:25620203	PCS		5/11			C	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0000938	PMID:25620203	PCS		1/8			P	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0011462	PMID:25620203	PCS		2/11			C	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0025526	PMID:25620203	PCS		7/11			P	HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0000006	PMID:25620203	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0000501	PMID:25620203	PCS		10/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-10]
OMIM:616298	Singleton-Merten syndrome 2		HP:0000962	PMID:25620203	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-10]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0000286	PMID:28306229	PCS					P	HPO:probinson[2019-05-22]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0001374	PMID:20847697	IEA		HP:0040284			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0001762	OMIM:130010	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0031869	PMID:11377605	PCS		3/4			P	HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0002761	OMIM:130010	IEA					P	HPO:skoehler[2019-09-07]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0001030	PMID:28306229	PCS					P	HP:probinson[2019-05-11]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0001382	PMID:11377605;PMID:28306229	PCS		14/14			P	HP:probinson[2019-05-11];HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0001073	PMID:28306229	PCS					P	HPO:probinson[2019-05-22]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0025014	PMID:11377605;PMID:28306229	PCS		12/14			P	HPO:probinson[2019-05-22];HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0001075	PMID:11377605	PCS		4/4			P	HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0100790	PMID:28306229	PCS					P	HP:probinson[2019-05-11];HP:probinson[2019-05-11]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0011108	PMID:4023980	PCS		2/6			P	HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0000978	PMID:28306229	PCS					P	HP:probinson[2019-05-11]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0000977	PMID:11377605	IEA		4/4			P	HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0001027	PMID:28306229	PCS					P	HP:probinson[2019-05-11];HP:probinson[2019-05-11]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0000993	PMID:11377605;PMID:28306229	PCS		12/14			P	HP:probinson[2019-05-11];HP:probinson[2019-05-11];HPO:probinson[2021-01-26]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0000006	PMID:9783710	PCS					I	HP:probinson[2019-05-11];HP:probinson[2019-05-11]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0000974	PMID:28306229	PCS					P	HP:probinson[2019-05-11]
OMIM:130010	Ehlers-Danlos syndrome, classic type, 2		HP:0002105	PMID:4023980	PCS		2/6			P	HPO:probinson[2021-01-26]
OMIM:615961	Acid-labile subunit, deficiency of		HP:0001530	PMID:21396577	PCS					P	HPO:skoehler[2015-09-15]
OMIM:615961	Acid-labile subunit, deficiency of		HP:0030353	PMID:21396577	PCS					P	HPO:skoehler[2015-09-15]
OMIM:615961	Acid-labile subunit, deficiency of		HP:0008189	PMID:21396577	PCS					P	HPO:skoehler[2015-09-15]
OMIM:615961	Acid-labile subunit, deficiency of		HP:0045046	PMID:14762184	PCS		1/1			P	HPO:skoehler[2015-09-15];HPO:probinson[2021-05-14]
OMIM:615961	Acid-labile subunit, deficiency of		HP:0000823	PMID:21396577	PCS					P	HPO:skoehler[2015-09-15]
OMIM:252605	Mucolipidosis III gamma		HP:0001650	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0007759	OMIM:252605	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252605	Mucolipidosis III gamma		HP:0004322	PMID:20034096	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0003333	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0003370	PMID:20034096	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0000280	PMID:20034096	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0034337	PMID:20034096	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0034681	PMID:20034096	PCS		3/3			P	HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0008155	PMID:20034096	PCS		0/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0003307	PMID:20034096	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0002857	PMID:20034096	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0001763	PMID:20034096	PCS		3/3			P	HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0001249	PMID:20034096	PCS		0/3			P	HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0003621	PMID:20034096	PCS		3/3			C	HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0002650	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0001387	PMID:20034096	PCS		3/3			P	HPO:skoehler[2013-06-06]
OMIM:252605	Mucolipidosis III gamma		HP:0000470	PMID:20034096	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0034665	PMID:20034096	PCS		3/3			P	HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0002829	PMID:20034096	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0002808	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0002869	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0000943	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0000007	PMID:20034096	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252605	Mucolipidosis III gamma		HP:0003538	OMIM:252605	TAS					P	HPO:skoehler[2017-07-13]
OMIM:252605	Mucolipidosis III gamma		HP:0000768	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0001659	OMIM:252605	IEA					P	HPO:iea[2009-02-17]
OMIM:252605	Mucolipidosis III gamma		HP:0000545	PMID:20034096	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-09]
OMIM:234580	Heimler syndrome 1		HP:0007814	PMID:26387595	PCS		7/12			P	HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0000705	PMID:26387595	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0000407	PMID:26387595	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0006297	PMID:26387595	PCS		14/14			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0003593	PMID:26387595	PCS		14/14			C	HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0000007	PMID:26387595	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0007754	PMID:26387595	PCS		2/12			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0041093	PMID:26387595	PCS		7/14			P	HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0001249	PMID:26387595	PCS		0/14			P	HPO:probinson[2023-04-14]
OMIM:234580	Heimler syndrome 1		HP:0001820	PMID:26387595	PCS		4/14			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-14]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0002135	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0003202	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0000750	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0001371	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0001890	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0002240	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0003593	PMID:30664889	IEA		1/1			C	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0001270	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0010783	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0009064	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0000969	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0033331	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0100614	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0000007	PMID:30664889	PCS					I	HPO:probinson[2021-04-03];HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0002716	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0001954	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0012490	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619183	Proteasome-associated autoinflammatory syndrome 4		HP:0001744	PMID:30664889	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000341	PMID:29100095	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0002069	PMID:29100095	PCS		7/10			P	HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0002540	PMID:29100095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000463	PMID:29100095	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001310	PMID:29100095	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0002186	PMID:29100095	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001272	PMID:29100095	PCS		9/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0002066	PMID:29100095	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0002121	PMID:29100095	PCS		1/10			P	HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001252	PMID:29100095	PCS		10/10			P	HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0003593	PMID:29100095	IEA					C	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0032794	PMID:29100095	PCS		4/10			P	HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000639	PMID:29100095	PCS		8/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000938	PMID:29100095	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0011220	PMID:29100095	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001249	PMID:29100095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001347	PMID:29100095	PCS		6/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000750	PMID:29100095	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0002353	PMID:29100095	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001321	PMID:29100095	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001260	PMID:29100095	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0010819	PMID:29100095	PCS		2/10			P	HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001263	PMID:29100095	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000007	PMID:29100095	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000648	PMID:29100095	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000505	PMID:29100095	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001257	PMID:29100095	PCS		4/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0000545	PMID:29100095	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:617810	Glycosylphosphatidylinositol biosynthesis defect 15		HP:0001337	PMID:29100095	PCS		5/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-05]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003554	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003577	PMID:10195214	PCS		2/2			C	HPO:probinson[2022-11-10]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0010628	OMIM:608930	TAS					P	HPO:skoehler[2015-05-31]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0001252	OMIM:608930	TAS					P	HPO:probinson[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003593	OMIM:608930	IEA					C	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003690	PMID:10195214	PCS		2/2			P	HPO:probinson[2022-11-10]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0001270	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003391	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0030319	PMID:10195214	PCS		2/2			P	HPO:probinson[2022-11-10]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000218	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000597	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003402	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003403	PMID:10195214	PCS		2/2			P	HPO:probinson[2022-11-10]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0002015	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003324	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0002650	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0003388	PMID:10195214	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0001283	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0001260	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0002033	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0030208	PMID:10195214	PCS		0/2			P	HPO:probinson[2022-11-10]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000508	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0002804	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000007	OMIM:608930	IEA					I	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0001319	OMIM:608930	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0002747	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000400	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000006	OMIM:608930	IEA					I	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000347	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0001612	OMIM:608930	IEA					P	HPO:iea[2009-02-17]
OMIM:608930	Myasthenic syndrome, congenital, 1B, fast-channel		HP:0000467	PMID:10195214	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-11-10]
OMIM:131440	Myeloproliferative disorder, chronic, with eosinophilia		HP:0001880	OMIM:131440	IEA					P	HPO:skoehler[2015-01-27]
OMIM:131440	Myeloproliferative disorder, chronic, with eosinophilia		HP:0006782	OMIM:131440	TAS					P	HPO:skoehler[2009-02-17]
OMIM:131440	Myeloproliferative disorder, chronic, with eosinophilia		HP:0000006	OMIM:131440	TAS					I	HPO:skoehler[2009-02-17]
OMIM:131440	Myeloproliferative disorder, chronic, with eosinophilia		HP:0005547	OMIM:131440	TAS					P	HPO:skoehler[2009-02-17]
OMIM:210350	Biemond syndrome II		HP:0001177	OMIM:210350	IEA					P	HPO:iea[2009-02-17]
OMIM:210350	Biemond syndrome II		HP:0000818	OMIM:210350	IEA					P	HPO:iea[2009-02-17]
OMIM:210350	Biemond syndrome II		HP:0004322	OMIM:210350	IEA					P	HPO:iea[2009-02-17]
OMIM:210350	Biemond syndrome II		HP:0000007	OMIM:210350	IEA					I	HPO:iea[2009-02-17]
OMIM:210350	Biemond syndrome II		HP:0000238	OMIM:210350	IEA					P	HPO:iea[2009-02-17]
OMIM:210350	Biemond syndrome II		HP:0000612	OMIM:210350	IEA					P	HPO:iea[2009-02-17]
OMIM:210350	Biemond syndrome II		HP:0001249	OMIM:210350	IEA					P	HPO:iea[2009-02-17]
OMIM:612968	Cataract 34, multiple types		HP:0007957	PMID:17893665	PCS					P	HPO:probinson[2025-10-03]
OMIM:612968	Cataract 34, multiple types		HP:0003577	PMID:17893665	PCS					C	HPO:probinson[2025-10-03]
OMIM:612968	Cataract 34, multiple types		HP:0000639	PMID:17893665	PCS					P	HPO:probinson[2025-10-03]
OMIM:612968	Cataract 34, multiple types		HP:0003593	PMID:17893665	PCS					C	HPO:probinson[2025-10-03]
OMIM:612968	Cataract 34, multiple types		HP:0000007	PMID:27218149	PCS					I	HPO:probinson[2025-10-03];HPO:probinson[2025-10-03]
OMIM:612968	Cataract 34, multiple types		HP:0010922	PMID:17893665	PCS					P	HPO:probinson[2025-10-03]
OMIM:612968	Cataract 34, multiple types		HP:0007787	PMID:17893665	PCS					P	HPO:probinson[2025-10-03]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000286	PMID:29100085	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000486	PMID:29100085	PCS		6/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001212	PMID:29100085	PCS		2/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0002540	PMID:29100085	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0002188	PMID:29100085	PCS		6/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001332	PMID:29100085	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001250	PMID:29100085	PCS		3/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0010808	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001252	PMID:29100085	PCS		12/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0003593	PMID:29100085	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001251	PMID:29100085	PCS		6/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0045074	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000319	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000957	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000954	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001763	PMID:29100085	PCS		3/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001169	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000358	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001249	PMID:29100085	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001265	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0003763	PMID:29100085	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000252	PMID:29100085	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000494	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001344	PMID:29100085	PCS		10/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001382	PMID:29100085	PCS		6/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0011968	PMID:29100085	PCS		9/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001263	PMID:29100085	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0002072	PMID:29100085	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001182	PMID:29100085	PCS		2/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000729	PMID:29100085	PCS		7/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000400	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0009899	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000963	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000369	PMID:29100085	PCS		1/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000006	PMID:29100085	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001272	PMID:29100085	PCS		3/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0012724	PMID:29100085	PCS		2/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0001270	PMID:29100085	PCS		12/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0002119	PMID:29100085	PCS		6/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0012171	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000218	PMID:29100085	PCS		1/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000274	PMID:29100085	PCS		3/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0002059	PMID:29100085	PCS		4/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0002650	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000750	PMID:29100085	PCS		12/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000276	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000232	PMID:29100085	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0031936	PMID:29100085	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000194	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0005280	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0032988	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0011304	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000349	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000348	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000664	PMID:29100085	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0000303	PMID:29100085	PCS		1/12			P	HPO:probinson[2022-12-17]
OMIM:617804	Neurodevelopmental disorder with severe motor impairment and absent language		HP:0004305	PMID:29100085	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000286	PMID:35482014	PCS		4/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0002069	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0004322	PMID:35482014	PCS		4/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001252	PMID:35482014	PCS		4/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0002020	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0032794	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0045075	PMID:35482014	PCS		4/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0011220	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000637	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001522	PMID:35482014	PCS		1/5			C	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001763	PMID:35482014	PCS		1/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0002510	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001344	PMID:35482014	PCS		4/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0002870	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0011968	PMID:35482014	PCS		4/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000490	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001263	PMID:35482014	PCS		4/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0011800	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0100021	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001182	PMID:35482014	PCS		4/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0011003	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0034353	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0002509	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001698	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000006	PMID:35482014	PCS					I	HPO:probinson[2022-12-04]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000341	PMID:35482014	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000582	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0003577	PMID:35482014	PCS		2/5			C	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0030674	PMID:35482014	PCS		3/5			C	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000020	PMID:35482014	PCS		2/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0002280	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0012444	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0009085	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000337	PMID:35482014	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0002714	PMID:35482014	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000218	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000653	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001320	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000670	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001561	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000431	PMID:35482014	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0011625	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001838	PMID:35482014	PCS		1/4			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0033044	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000348	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001558	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0001631	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0000347	PMID:35482014	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:620070	Neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties		HP:0004942	PMID:35482014	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:310350	Myelolymphatic insufficiency		HP:0001882	OMIM:310350	TAS					P	HPO:probinson[2012-04-25]
OMIM:310350	Myelolymphatic insufficiency		HP:0001419	OMIM:310350	TAS					I	HPO:probinson[2012-04-25]
OMIM:310350	Myelolymphatic insufficiency		HP:0002718	OMIM:310350	TAS					P	HPO:probinson[2012-04-25]
OMIM:310350	Myelolymphatic insufficiency		HP:0004429	OMIM:310350	TAS					P	HPO:probinson[2012-04-25]
OMIM:310350	Myelolymphatic insufficiency		HP:0011447	OMIM:310350	TAS					P	HPO:probinson[2012-04-25]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000582	OMIM:300143	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0010804	OMIM:300143	TAS					P	HPO:probinson[2012-07-24]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000486	PMID:21484992	PCS		2/5			P	HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0001250	PMID:21484992	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000194	OMIM:300143	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0001382	PMID:21484992	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0003196	OMIM:300143	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000053	PMID:21484992	PCS		1/4			P	HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0009909	OMIM:300143	TAS					P	HPO:probinson[2012-07-24]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0100710	PMID:21484992	PCS		2/5			P	HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0001419	PMID:21484992	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000717	OMIM:300143	TAS					P	HPO:probinson[2012-07-24]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000316	OMIM:300143	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000678	OMIM:300143	TAS					P	HPO:probinson[2012-07-24]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000664	PMID:21484992	PCS		3/5			P	HPO:probinson[2012-07-24];HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000752	OMIM:300143	TAS					P	HPO:probinson[2012-07-24]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0000303	PMID:21484992	PCS		4/5			P	HPO:probinson[2012-07-24];HPO:probinson[2019-12-10]
OMIM:300143	Intellectual developmental disorder, X-linked 21		HP:0001611	PMID:21484992	PCS		2/5			P	HPO:probinson[2019-12-10]
OMIM:150900	LENTIGINES		HP:0000639	OMIM:150900	IEA					P	HPO:iea[2009-02-17]
OMIM:150900	LENTIGINES		HP:0000006	OMIM:150900	IEA					I	HPO:iea[2009-02-17]
OMIM:150900	LENTIGINES		HP:0000951	OMIM:150900	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001596	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001251	OMIM:127550	IEA					P	HPO:skoehler[2010-06-18]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001394	PMID:11574891	PCS		2/12			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0008070	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0000939	OMIM:127550	IEA					P	HPO:skoehler[2010-06-18]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001903	PMID:11574891	PCS		6/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001807	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001328	OMIM:127550	IEA					P	HPO:skoehler[2010-06-18]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001888	OMIM:127550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0002639	PMID:11574891	PCS		1/12			P	HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001803	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0007588	PMID:11574891	PCS		10/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0005528	OMIM:127550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0002216	PMID:11574891	PCS		4/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0006515	PMID:11574891	PCS		1/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0000670	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0004334	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001321	OMIM:127550	IEA					P	HPO:skoehler[2010-06-18]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001882	PMID:11574891	PCS		7/12			P	HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0006739	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0002094	PMID:11574891	PCS		1/12			P	HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0006480	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001915	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0002605	PMID:11574891	PCS		1/12			P	HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0005518	PMID:11574891	PCS		11/12			P	HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0008404	PMID:11574891	PCS		8/10			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0002745	PMID:11574891	PCS		4/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0002206	PMID:11574891	PCS		3/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0001873	PMID:11574891	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0000006	PMID:11574891	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1		HP:0002863	OMIM:127550	IEA					P	HPO:iea[2009-02-17]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0002553	OMIM:609384	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0001491	OMIM:609384	TAS					P	HPO:probinson[2009-02-17]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0002808	OMIM:609384	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0009891	OMIM:609384	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0000767	OMIM:609384	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0000219	OMIM:609384	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0000006	OMIM:609384	IEA					I	HPO:iea[2009-02-17]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0001249	OMIM:609384	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0007867	OMIM:609384	IEA					P	HPO:iea[2009-02-17]
OMIM:609384	Fibrosis of extraocular muscles, congenital, 3B		HP:0007911	OMIM:609384	IEA					P	HPO:iea[2009-02-17]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001298	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002321	PMID:22152682	PCS					P	HPO:skoehler[2013-06-06];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001332	PMID:22152682	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001250	PMID:22152682	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002066	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001252	PMID:22152682	PCS		1/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002283	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0003593	PMID:22152682	PCS		2/5			C	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001251	PMID:22152682	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002061	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002080	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0012402	PMID:22152682	PCS		4/5			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0000639	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0011463	PMID:22152682	PCS		3/5			C	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0020221	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0003128	PMID:22152682	PCS		3/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0000252	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002078	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0000750	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001288	PMID:22152682	PCS		3/10			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002376	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002131	PMID:22152682	PCS		2/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001260	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002371	PMID:22152682	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002151	PMID:22152682	PCS		2/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001263	PMID:22152682	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0002490	PMID:22152682	PCS		2/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001618	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0000602	PMID:22152682	PCS		1/5			P	HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001712	PMID:22152682	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0000007	PMID:22152682	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614458	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)		HP:0001257	PMID:22152682	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:112500	Brachydactyly, type A1		HP:0004279	OMIM:112500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:112500	Brachydactyly, type A1		HP:0004322	ISBN-13:978-3437214301	PCS					P	HPO:iea[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0001156	OMIM:112500	IEA					P	HPO:skoehler[2015-01-19]
OMIM:112500	Brachydactyly, type A1		HP:0001032	OMIM:112500	PCS					P	HPO:iea[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0010049	ISBN-13:978-3437214301	PCS					P	HPO:iea[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0005194	ISBN-13:978-3437214301	PCS					P	HPO:skoehler[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0010107	ISBN-13:978-3437214301	PCS					P	HPO:iea[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0010194	ISBN-13:978-3437214301	PCS					P	HPO:iea[2009-10-20]
OMIM:112500	Brachydactyly, type A1		HP:0009462	OMIM:112500	TAS					P	HPO:iea[2009-10-20]
OMIM:112500	Brachydactyly, type A1		HP:0009882	OMIM:112500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:112500	Brachydactyly, type A1		HP:0006165	OMIM:112500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:112500	Brachydactyly, type A1		HP:0009467	OMIM:112500	TAS					P	HPO:iea[2009-10-20]
OMIM:112500	Brachydactyly, type A1		HP:0009279	OMIM:112500	TAS					P	HPO:iea[2009-10-20]
OMIM:112500	Brachydactyly, type A1		HP:0006146	OMIM:112500	TAS					P	HPO:skoehler[2013-04-14]
OMIM:112500	Brachydactyly, type A1		HP:0009843	ISBN-13:978-3437214301	PCS					P	HPO:iea[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0006213	OMIM:112500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:112500	Brachydactyly, type A1		HP:0004209	OMIM:112500	PCS					P	HPO:iea[2009-10-20]
OMIM:112500	Brachydactyly, type A1		HP:0006236	OMIM:112500	TAS					P	HPO:skoehler[2013-04-14]
OMIM:112500	Brachydactyly, type A1		HP:0001169	OMIM:112500	TAS					P	HPO:skoehler[2013-04-07]
OMIM:112500	Brachydactyly, type A1		HP:0009638	ISBN-13:978-3437214301	PCS					P	HPO:iea[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0000006	OMIM:112500	PCS					I	HPO:iea[2012-04-24]
OMIM:112500	Brachydactyly, type A1		HP:0001204	OMIM:112500	PCS					P	HPO:iea[2012-04-24]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000054	PMID:31079898	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000276	PMID:31079898	PCS		2/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000122	PMID:31079898	PCS		1/7			P	HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0001250	PMID:31079898	PCS		6/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000490	PMID:31079898	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0001263	PMID:31079898	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0004392	PMID:31079898	PCS	HP:0003577	2/7			P	HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0001090	PMID:31079898	PCS		1/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0011094	PMID:31079898	PCS		1/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0001629	PMID:31079898	PCS	HP:0003577	1/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0034454	PMID:31079898	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000007	PMID:31079898	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000733	PMID:31079898	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000400	PMID:31079898	PCS		2/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0007018	PMID:31079898	PCS		2/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000256	PMID:31079898	PCS		2/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0000028	PMID:31079898	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618504	Intellectual developmental disorder, autosomal recessive 71		HP:0001249	PMID:31079898	PCS		7/7			P	HPO:probinson[2022-12-03]
OMIM:617637	Deafness, autosomal recessive 106		HP:0000365	PMID:26282398	PCS	HP:0011463	2/2			P	HPO:probinson[2019-06-13]
OMIM:617637	Deafness, autosomal recessive 106		HP:0000007	PMID:26282398	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:610158	Corneal dystrophy, fuchs endothelial, 2		HP:0007705	OMIM:610158	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610158	Corneal dystrophy, fuchs endothelial, 2		HP:0000969	OMIM:610158	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610158	Corneal dystrophy, fuchs endothelial, 2		HP:0001131	OMIM:610158	IEA					P	HPO:skoehler[2015-01-19]
OMIM:610158	Corneal dystrophy, fuchs endothelial, 2		HP:0012038	OMIM:610158	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610158	Corneal dystrophy, fuchs endothelial, 2		HP:0000006	OMIM:610158	TAS					I	HPO:skoehler[2012-10-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000486	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0004322	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0001252	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0001274	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0001290	OMIM:109120	TAS					P	HPO:skoehler[2017-07-13]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0012368	OMIM:109120	TAS					P	HPO:skoehler[2013-10-22]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000316	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000558	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000238	OMIM:109120	IEA					P	HPO:skoehler[2015-12-30]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0002119	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0007886	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000256	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0001249	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0002673	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0006958	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0002690	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000272	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000925	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000407	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000506	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0002827	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000327	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0007873	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000520	OMIM:109120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000006	OMIM:109120	IEA					I	HPO:iea[2009-02-17]
OMIM:109120	Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities		HP:0000248	OMIM:109120	IEA					P	HPO:iea[2009-02-17]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0003676	PMID:20362274	PCS					C	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001250	PMID:20362274	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001271	PMID:20362274	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001252	PMID:20362274	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0003593	PMID:20362274	PCS		2/2			C	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0000737	PMID:20362274	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001308	PMID:20362274	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001324	PMID:20362274	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0003202	PMID:20362274	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001265	PMID:20362274	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0003200	PMID:20362274	PCS		1/1			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002375	PMID:20362274	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0003542	PMID:20362274	PCS		1/1			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002376	PMID:20362274	PCS	HP:0003593	2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002134	OMIM:300816	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002197	PMID:20362274	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002151	PMID:20362274	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001263	PMID:20362274	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001284	PMID:20362274	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002490	PMID:20362274	PCS		1/1			P	HPO:skoehler[2012-10-15];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0001419	PMID:20362274	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0007178	PMID:20362274	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0008347	PMID:20362274	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002747	PMID:20362274	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0002445	PMID:20362274	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:300816	Combined oxidative phosphorylation deficiency 6		HP:0004305	PMID:20362274	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-06-03]
OMIM:613451	Frontonasal dysplasia 2		HP:0000486	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0012745	OMIM:613451	TAS					P	HPO:skoehler[2015-05-31]
OMIM:613451	Frontonasal dysplasia 2		HP:0031585	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0010761	PMID:19692347	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0045075	OMIM:613451	TAS		20/20			P	HPO:probinson[2022-05-08];HPO:skoehler[2015-05-31]
OMIM:613451	Frontonasal dysplasia 2		HP:0003191	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0011220	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0011461	PMID:19692347	PCS		1/2			C	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000316	PMID:19692347	PCS		2/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000437	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0001249	OMIM:613451	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:613451	Frontonasal dysplasia 2		HP:0000633	OMIM:613451	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:613451	Frontonasal dysplasia 2		HP:0002335	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0001583	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0003764	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000252	PMID:19692347	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0002079	OMIM:613451	TAS					P	HPO:skoehler[2014-10-06]
OMIM:613451	Frontonasal dysplasia 2		HP:0001263	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0012811	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0011326	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000568	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000007	PMID:19692347	PCS					I	HPO:skoehler[2016-02-01];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000966	OMIM:613451	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:613451	Frontonasal dysplasia 2		HP:0000289	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0008689	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000369	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000248	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000687	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000582	OMIM:613451	TAS					P	HPO:skoehler[2014-10-06]
OMIM:613451	Frontonasal dysplasia 2		HP:0007418	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0003577	PMID:19692347	PCS		1/2			C	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000463	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000581	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0010544	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0002084	PMID:19692347	PCS		1/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0008070	PMID:19692347	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0010941	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000653	OMIM:613451	TAS					P	HPO:skoehler[2015-05-31]
OMIM:613451	Frontonasal dysplasia 2		HP:0000457	OMIM:613451	TAS					P	HPO:skoehler[2014-10-06]
OMIM:613451	Frontonasal dysplasia 2		HP:0000698	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000456	PMID:19692347	PCS		2/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0001562	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0001320	OMIM:613451	TAS					P	HPO:skoehler[2014-10-06]
OMIM:613451	Frontonasal dysplasia 2		HP:0002697	PMID:19692347	PCS		1/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0002213	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0001363	OMIM:613451	TAS					P	HPO:skoehler[2014-10-06]
OMIM:613451	Frontonasal dysplasia 2		HP:0000431	PMID:19692347	PCS		2/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0001362	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0005280	OMIM:613451	TAS					P	HPO:skoehler[2014-10-06]
OMIM:613451	Frontonasal dysplasia 2		HP:0000506	PMID:19692347	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0001511	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:613451	Frontonasal dysplasia 2		HP:0000666	PMID:19692347	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:612997	Spermatogenic failure 7		HP:0003251	PMID:19344877	PCS		2/2			P	HPO:probinson[2013-02-23];HPO:probinson[2022-12-14]
OMIM:612997	Spermatogenic failure 7		HP:0011462	PMID:19344877	PCS		2/2			C	HPO:probinson[2022-12-14]
OMIM:612997	Spermatogenic failure 7		HP:0000007	PMID:19344877	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-12-14]
OMIM:612997	Spermatogenic failure 7		HP:0012207	PMID:19344877	PCS		2/2			P	HPO:probinson[2013-03-12];HPO:probinson[2022-12-14]
OMIM:612997	Spermatogenic failure 7		HP:0012208	PMID:19344877	PCS		1/2			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-12-14]
OMIM:612997	Spermatogenic failure 7		HP:0000798	PMID:19344877	PCS		2/2			P	HPO:probinson[2013-02-23];HPO:probinson[2022-12-14]
OMIM:615034	Dystonia 24		HP:0000473	PMID:23200863	PCS		8/8			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0003621	PMID:23200863	PCS		1/8			C	HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0011462	PMID:23200863	PCS		7/8			C	HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0003829	PMID:23200863	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0031960	PMID:23200863	PCS		4/8			P	HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0012048	PMID:23200863	PCS		2/8			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0000006	PMID:23200863	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0002346	PMID:23200863	PCS		1/8			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0000643	PMID:23200863	PCS		1/8			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-11]
OMIM:615034	Dystonia 24		HP:0200085	PMID:23200863	PCS		7/8			P	HPO:probinson[2022-12-11]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0005203	OMIM:277320	IEA					P	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0001939	OMIM:277320	IEA					P	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0000508	OMIM:277320	IEA					P	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0004395	OMIM:277320	IEA					P	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0000602	OMIM:277320	IEA					P	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0009830	OMIM:277320	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0000007	OMIM:277320	IEA					I	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0002617	OMIM:277320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0003270	OMIM:277320	IEA					P	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0002027	OMIM:277320	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0002578	OMIM:277320	TAS					P	HPO:iea[2009-02-17]
OMIM:277320	Visceral myopathy, familial, with external ophthalmoplegia		HP:0000544	OMIM:277320	TAS					P	HPO:skoehler[2015-01-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0001265	PMID:18817903	PCS		8/8		HP:0025215	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0003236	PMID:18817903	PCS		8/8		HP:0025215	P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0003621	PMID:18817903	PCS		1/3			C	HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0002153	OMIM:268200	IEA					P	HPO:iea[2009-02-17]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0001284	PMID:18817903	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0001919	OMIM:268200	IEA					P	HPO:iea[2009-02-17]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0011463	PMID:18817903	PCS		7/8			C	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0002913	PMID:18817903	PCS		8/8		HP:0025215	P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0000007	PMID:18817903	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0001945	OMIM:268200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0025435	PMID:18817903	PCS		3/3		HP:0025215	P	HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0001324	PMID:18817903	PCS		8/8		HP:0025215	P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0008942	PMID:18817903	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-08-21]
OMIM:268200	Myoglobinuria, acute recurrent, autosomal recessive		HP:0003326	PMID:18817903	PCS		8/8		HP:0025215	P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0006944	PMID:35411967	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0002650	PMID:35411967	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000486	OMIM:608703	IEA					P	HPO:iea[2009-02-17]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000365	PMID:35411967	PCS		3/4			P	HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0003487	PMID:35411967	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0001761	PMID:35411967	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000012	PMID:35411967	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0002013	PMID:35411967	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0001272	PMID:35411967	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0001260	PMID:35411967	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0001251	PMID:35411967	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0011468	PMID:35411967	PCS		1/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0003380	PMID:35411967	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000639	PMID:35411967	PCS		7/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000657	PMID:35411967	PCS		1/11			P	HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0007663	OMIM:608703	TAS					P	HPO:skoehler[2015-07-26]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000505	OMIM:608703	IEA					P	HPO:iea[2009-02-17]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000317	OMIM:608703	IEA					P	HPO:iea[2009-02-17]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000763	PMID:35411967	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0002522	PMID:35411967	PCS		7/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0000006	PMID:35411967	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0002500	PMID:35411967	PCS		2/10			P	HPO:probinson[2022-08-21]
OMIM:608703	Spinocerebellar ataxia 25		HP:0007328	OMIM:608703	IEA					P	HPO:iea[2009-02-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0002059	OMIM:611252	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0001761	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0001288	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0003487	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0002079	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0001272	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0002064	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0002061	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0011448	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0007340	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0011463	OMIM:611252	TAS					C	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0000007	OMIM:611252	TAS					I	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0001258	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0003677	OMIM:611252	TAS					C	HPO:skoehler[2012-10-17]
OMIM:611252	Spastic paraplegia 32, autosomal recessive		HP:0001347	OMIM:611252	TAS					P	HPO:probinson[2012-04-17]
OMIM:300802	Intellectual developmental disorder, X-linked 96		HP:0001250	PMID:19377476	PCS		HP:0040283			P	HPO:skoehler[2012-11-16];HPO:probinson[2021-09-26]
OMIM:300802	Intellectual developmental disorder, X-linked 96		HP:0001419	PMID:19377476	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-26]
OMIM:300802	Intellectual developmental disorder, X-linked 96		HP:0001249	PMID:19377476	PCS		3/3			P	HPO:skoehler[2012-11-16];HPO:probinson[2021-09-26];HPO:probinson[2022-07-03]
OMIM:225300	Split-Hand/foot malformation 6		HP:0001770	PMID:18515319	PCS					P	HPO:iea[2010-04-23]
OMIM:225300	Split-Hand/foot malformation 6		HP:0001849	PMID:18515319	PCS					P	HPO:iea[2010-04-23]
OMIM:225300	Split-Hand/foot malformation 6		HP:0001839	PMID:18515319	PCS					P	HPO:iea[2009-02-17]
OMIM:225300	Split-Hand/foot malformation 6		HP:0003829	PMID:18515319	PCS					I	HPO:iea[2010-04-23]
OMIM:225300	Split-Hand/foot malformation 6		HP:0000007	PMID:18515319;OMIM:225300	PCS					I	HPO:iea[2012-04-24]
OMIM:225300	Split-Hand/foot malformation 6		HP:0006101	PMID:18515319	PCS					P	HPO:iea[2010-04-23]
OMIM:225300	Split-Hand/foot malformation 6		HP:0001171	PMID:18515319	PCS					P	HPO:iea[2010-04-23]
OMIM:225300	Split-Hand/foot malformation 6		HP:0009380	PMID:18515319	PCS					P	HPO:iea[2010-04-23]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0006989	PMID:30420557	PCS		5/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0003676	PMID:30420557	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0003577	PMID:30420557	PCS		1/13			C	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0002540	PMID:30420557	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0000486	PMID:30420557	PCS		8/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001332	PMID:30420557	PCS		4/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001272	PMID:30420557	PCS		13/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001252	PMID:30420557	PCS		13/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0002283	PMID:30420557	PCS		1/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001251	PMID:30420557	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0003593	PMID:30420557	PCS		11/13			C	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001270	PMID:30420557	PCS		13/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0011410	PMID:30420557	PCS		7/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0012110	PMID:30420557	PCS		1/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001508	PMID:30420557	PCS		3/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0000639	PMID:30420557	PCS		3/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0011463	PMID:30420557	PCS		1/13			C	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0000817	PMID:30420557	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0000514	PMID:30420557	PCS		2/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0007002	PMID:30420557	PCS		5/6			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001308	PMID:30420557	PCS		4/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0003803	PMID:30420557	PCS		2/3			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001324	PMID:30420557	PCS		13/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0003202	PMID:30420557	PCS		6/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0025331	PMID:30420557	PCS		2/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0000252	PMID:30420557	PCS		8/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001344	PMID:30420557	PCS		5/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0002376	PMID:30420557	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0011968	PMID:30420557	PCS		8/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001263	PMID:30420557	PCS		13/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0002273	PMID:30420557	PCS		5/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0000007	PMID:30420557	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0002747	PMID:30420557	PCS		4/13			P	HPO:probinson[2022-06-25]
OMIM:618276	Neurodegeneration, childhood-onset, with cerebellar atrophy		HP:0001257	PMID:30420557	PCS		6/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-25]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0003676	PMID:27545679	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0000365	PMID:27545679	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001310	PMID:29959261	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001332	PMID:27545679	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001288	PMID:27545679	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001272	PMID:27545679	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001260	PMID:27545679;PMID:29959261	PCS		20/20			P	HPO:probinson[2022-03-19];HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0002066	PMID:27545679	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0000020	PMID:27545679	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0002075	PMID:29959261	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001251	PMID:27545679;PMID:29959261	PCS		20/20			P	HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0002070	PMID:27545679	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0100660	PMID:29959261	PCS		4/11			P	HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0100543	PMID:29959261	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0000639	PMID:29959261	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0000815	PMID:29959261	PCS		2/2			P	HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0000657	PMID:27545679	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0007256	PMID:27545679	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0000007	PMID:27545679	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001268	PMID:27545679	PCS		8/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001337	PMID:27545679	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0001347	PMID:29959261	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:617145	Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset		HP:0000511	PMID:27545679;PMID:29959261	PCS		18/20			P	HPO:probinson[2022-03-19];HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0012650	PMID:24531968	PCS		5/5			P	HPO:skoehler[2015-09-13];HPO:probinson[2020-07-24];HPO:probinson[2024-03-15]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0002463	PMID:24531968	PCS		5/5			P	HPO:skoehler[2015-09-13];HPO:probinson[2020-07-24];HPO:probinson[2024-03-15]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0001250	PMID:24531968	PCS		5/5			P	HPO:skoehler[2015-09-13];HPO:probinson[2020-07-24];HPO:probinson[2024-03-15]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0003593	PMID:24531968	PCS					C	HPO:probinson[2020-07-24]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0000007	PMID:24531968	PCS					I	HPO:skoehler[2015-09-13];HPO:probinson[2020-07-24]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0001270	PMID:24531968	PCS		0/5			P	HPO:skoehler[2015-09-13];HPO:probinson[2020-07-24]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0001249	PMID:24531968	PCS		4/5			P	HPO:skoehler[2015-09-13];HPO:probinson[2020-07-24];HPO:probinson[2024-03-15]
OMIM:615752	Polymicrogyria, bilateral perisylvian		HP:0000577	PMID:24531968	PCS		1/5			P	HPO:probinson[2024-03-15]
OMIM:300194	AMME complex		HP:0004445	PMID:9598718	PCS		2/4			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0000483	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001212	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0000023	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001252	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0003593	PMID:9598718	PCS		2/4			C	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0012803	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0011463	PMID:9598718	PCS		1/4			C	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0000219	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001466	PMID:9598718	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0005824	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001249	PMID:9598718	PCS		2/4			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001540	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0000331	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001382	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0000790	PMID:9598718	PCS		4/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001263	PMID:9598718	PCS		2/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0003581	PMID:9598718	PCS		1/4			C	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0011800	PMID:9598718	PCS		2/4			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0005280	PMID:9598718	PCS		2/4			P	HPO:probinson[2022-06-01];HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0032988	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0000407	PMID:9598718	PCS		2/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001537	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001417	PMID:9598718	PCS					I	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001852	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:300194	AMME complex		HP:0001511	PMID:9598718	PCS		1/4			P	HPO:probinson[2022-06-01]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0031405	OMIM:224750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0001792	OMIM:224750	IEA					P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0002860	OMIM:224750	IEA					P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000320	OMIM:224750	IEA					P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0002671	OMIM:224750	IEA					P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0002231	PMID:19559398	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0011313	OMIM:224750	TAS					P	HPO:skoehler[2013-08-11]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0031454	OMIM:224750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0008070	PMID:19559398	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0034946	PMID:19559398	PCS		1/1			P	HPO:probinson[2023-07-18]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0001816	OMIM:224750	TAS					P	HPO:skoehler[2013-08-11]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000958	PMID:19559398	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000968	OMIM:224750	TAS					P	HPO:skoehler[2015-01-14]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0001807	OMIM:224750	IEA					P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0001806	OMIM:224750	IEA					P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000668	PMID:19559398	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000007	PMID:19559398	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0008404	PMID:19559398	PCS		1/1			P	HPO:probinson[2023-05-19];HPO:probinson[2023-05-19]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000982	PMID:19559398	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000962	PMID:19559398	PCS		1/1			P	HPO:probinson[2023-05-19];HPO:probinson[2023-05-19]
OMIM:224750	Schopf-Schulz-Passarge syndrome		HP:0000478	OMIM:224750	IEA					P	HPO:iea[2009-02-17]
OMIM:614464	Joubert syndrome 15		HP:0000054	OMIM:614464	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614464	Joubert syndrome 15		HP:0000062	OMIM:614464	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614464	Joubert syndrome 15		HP:0001263	PMID:22246503	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0001252	PMID:22246503	PCS		4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0001251	OMIM:614464	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614464	Joubert syndrome 15		HP:0001290	OMIM:614464	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614464	Joubert syndrome 15		HP:0000090	PMID:22246503	PCS		0/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0030769	PMID:22246503	PCS		1/5			P	HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0100258	PMID:22246503	PCS		1/5			P	HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0000657	PMID:22246503	PCS		3/4			P	HPO:skoehler[2012-11-28];HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0000007	PMID:22246503	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0002419	PMID:22246503	PCS		4/4			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0000488	PMID:22246503	PCS		0/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-04-06]
OMIM:614464	Joubert syndrome 15		HP:0001249	OMIM:614464	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614464	Joubert syndrome 15		HP:0000556	OMIM:614464	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614464	Joubert syndrome 15		HP:0000589	PMID:22246503	PCS		0/5			P	HPO:probinson[2023-04-06]
OMIM:269650	Secretory component deficiency		HP:0002254	OMIM:269650	TAS					P	HPO:probinson[2009-02-17]
OMIM:269650	Secretory component deficiency		HP:0004433	OMIM:269650	IEA					P	HPO:iea[2009-02-17]
OMIM:269650	Secretory component deficiency		HP:0005411	OMIM:269650	IEA					P	HPO:iea[2009-02-17]
OMIM:269650	Secretory component deficiency		HP:0000007	OMIM:269650	IEA					I	HPO:iea[2009-02-17]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0003256	OMIM:612015	TAS					P	HPO:probinson[2013-04-03]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0004322	OMIM:612015	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0002783	PMID:19701946	PCS		2/3			P	HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001250	PMID:19701946;PMID:18313027	PCS		4/4			P	HPO:probinson[2023-03-23];HPO:probinson[2013-04-03]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001252	PMID:19701946;PMID:18313027	PCS		4/4			P	HPO:probinson[2023-03-23];HPO:probinson[2013-04-03];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001251	OMIM:612015	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0002240	PMID:18313027	PCS		1/1			P	HPO:probinson[2013-04-03]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0003593	PMID:19701946	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001508	PMID:19701946	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0007663	PMID:19701946	PCS		3/3			P	HPO:skoehler[2015-08-16]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001347	OMIM:612015	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0003642	PMID:19701946	PCS		3/3			P	HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0000252	PMID:19701946	PCS		2/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0002059	PMID:19701946	PCS		1/3			P	HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0011968	PMID:19701946	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001263	PMID:18313027	PCS		1/1			P	HPO:probinson[2013-04-03];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0003186	PMID:19701946	PCS		2/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0000470	PMID:19701946	PCS		2/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001181	PMID:19701946	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0002093	PMID:19701946	PCS		2/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0008081	PMID:19701946	PCS		3/3			P	HPO:skoehler[2015-08-16]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0000407	PMID:19701946	PCS		3/3			P	HPO:skoehler[2015-08-16]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0000007	PMID:18313027	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001257	OMIM:612015	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0000347	PMID:19701946	PCS		2/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-23]
OMIM:612015	Congenital disorder of glycosylation, type In		HP:0001336	PMID:19701946	PCS		3/3			P	HPO:skoehler[2015-08-16]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0003202	PMID:21391237	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0001662	OMIM:614302	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0003581	PMID:21391237	PCS		2/2			C	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0003560	PMID:21391237	PCS					P	HPO:skoehler[2013-05-29];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0005110	PMID:21391237	PCS		1/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0007126	PMID:21391237	PCS		2/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0003701	PMID:21391237	PCS		2/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0003677	PMID:21391237	PCS					C	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0000006	PMID:21391237	PCS					I	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0000467	PMID:21391237	PCS		2/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-18]
OMIM:614302	Emery-Dreifuss muscular dystrophy 7, autosomal dominant		HP:0003557	PMID:21391237	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:616515	Deafness, autosomal recessive 104		HP:0003577	PMID:24958875	PCS		6/6			C	HPO:probinson[2022-05-14]
OMIM:616515	Deafness, autosomal recessive 104		HP:0001751	PMID:24958875	PCS		0/6			P	HPO:probinson[2022-05-14]
OMIM:616515	Deafness, autosomal recessive 104		HP:0000639	PMID:24958875	PCS		0/6			P	HPO:probinson[2022-05-14]
OMIM:616515	Deafness, autosomal recessive 104		HP:0004463	PMID:24958875	PCS		6/6			P	HPO:probinson[2022-05-14]
OMIM:616515	Deafness, autosomal recessive 104		HP:0001263	PMID:24958875	PCS		0/6			P	HPO:probinson[2022-05-14]
OMIM:616515	Deafness, autosomal recessive 104		HP:0000007	PMID:24958875	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-14]
OMIM:616515	Deafness, autosomal recessive 104		HP:0002403	PMID:24958875	PCS		0/6			P	HPO:probinson[2022-05-14]
OMIM:616515	Deafness, autosomal recessive 104		HP:0000399	PMID:24958875	PCS	HP:0003577	6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-14]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0003587	OMIM:600363	IEA					C	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0002169	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0003676	OMIM:600363	IEA					C	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0002166	OMIM:600363	TAS					P	HPO:probinson[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0000012	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0001761	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0003487	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0001250	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0000020	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0002064	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0002061	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0007340	OMIM:600363	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0003828	OMIM:600363	IEA					M	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0002839	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0001258	OMIM:600363	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0000006	OMIM:600363	IEA					I	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0001337	OMIM:600363	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0001347	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:600363	Spastic paraplegia 6, autosomal dominant		HP:0002314	OMIM:600363	IEA					P	HPO:iea[2009-02-17]
OMIM:606712	Specific language impairment 2		HP:0002474	OMIM:606712	IEA					P	HPO:iea[2009-02-17]
OMIM:606712	Specific language impairment 2		HP:0002463	OMIM:606712	IEA					P	HPO:skoehler[2015-01-27]
OMIM:606712	Specific language impairment 2		HP:0001426	OMIM:606712	IEA					I	HPO:iea[2009-02-17]
OMIM:606712	Specific language impairment 2		HP:0002526	OMIM:606712	IEA					P	HPO:iea[2009-02-17]
OMIM:606712	Specific language impairment 2		HP:0002549	OMIM:606712	IEA					P	HPO:iea[2009-02-17]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0003577	PMID:25339201	PCS		1/1			C	HPO:probinson[2022-03-26]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0002045	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0000331	PMID:25339201	PCS		1/1			P	HPO:skoehler[2015-08-05];HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0001252	PMID:25339201	PCS		1/1			P	HPO:skoehler[2015-08-05];HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0030682	PMID:25339201	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0012664	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0005180	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0001639	PMID:25339201	PCS		1/1			P	HPO:skoehler[2015-08-05];HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0000007	PMID:24549041	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-11]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0008347	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0001319	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0001659	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0001643	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0002789	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0001942	PMID:25339201	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:616501	Mitochondrial complex IV deficiency, nuclear type 13		HP:0003128	PMID:25339201	PCS		1/1			P	HPO:skoehler[2015-08-05];HPO:probinson[2021-07-05]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0031944	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0003565	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0003621	PMID:32238915	PCS		2/2			C	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0004840	PMID:32238915	PCS		2/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0002783	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0003212	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0100280	PMID:32238915	PCS		2/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0002099	PMID:32238915	PCS		2/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0002110	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0003493	PMID:32238915	PCS		1/1			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0032069	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0003261	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0032446	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0011227	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0034163	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-04-17]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0034174	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-04-17]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0034177	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-04-17]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0034165	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-04-17]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0034168	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-04-17]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0031891	PMID:32238915	PCS		2/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0000007	PMID:32238915	PCS					I	HPO:probinson[2022-01-29];HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0002923	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0003237	PMID:32238915	PCS		2/2			P	HPO:probinson[2022-01-29]
OMIM:619632	Immunodeficiency 89 and autoimmunity		HP:0034171	PMID:32238915	PCS		1/2			P	HPO:probinson[2022-04-17]
OMIM:118005	Cervical vertebral dysplasia		HP:0005678	OMIM:118005	TAS					P	HPO:probinson[2009-02-17]
OMIM:118005	Cervical vertebral dysplasia		HP:0008461	OMIM:118005	TAS					P	HPO:probinson[2009-02-17]
OMIM:118005	Cervical vertebral dysplasia		HP:0008469	OMIM:118005	TAS					P	HPO:probinson[2009-02-17]
OMIM:118005	Cervical vertebral dysplasia		HP:0000006	OMIM:118005	TAS					I	HPO:probinson[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0009937	OMIM:260660	IEA					P	HPO:skoehler[2010-06-18]
OMIM:260660	Cousin syndrome		HP:0000882	PMID:19068278	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000365	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000482	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0012745	OMIM:260660	TAS					P	HPO:skoehler[2014-03-24]
OMIM:260660	Cousin syndrome		HP:0011266	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0006077	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000316	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000238	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000358	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000175	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000890	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0002990	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000171	OMIM:260660	TAS					P	HPO:probinson[2012-07-16]
OMIM:260660	Cousin syndrome		HP:0000490	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0004692	OMIM:260660	TAS					P	HPO:probinson[2012-07-16]
OMIM:260660	Cousin syndrome		HP:0000294	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0004691	OMIM:260660	TAS					P	HPO:probinson[2012-07-16]
OMIM:260660	Cousin syndrome		HP:0003041	PMID:19068278	PCS	HP:0011463	2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0003083	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0012385	OMIM:260660	TAS					P	HPO:skoehler[2013-10-22]
OMIM:260660	Cousin syndrome		HP:0002827	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0008488	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000007	PMID:19068278	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000568	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0004209	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0002866	PMID:19068278	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000369	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000402	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000126	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0008905	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0003498	PMID:19068278	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0001591	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000061	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000581	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0003175	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0003173	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0009085	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0008472	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000256	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05];HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0000033	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0003027	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0001762	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000470	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0045025	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0009473	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0001239	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0002007	PMID:19068278	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:260660	Cousin syndrome		HP:0002324	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:260660	Cousin syndrome		HP:0000347	OMIM:260660	IEA					P	HPO:iea[2009-02-17]
OMIM:615008	Nephrotic syndrome, type 7		HP:0003774	PMID:23274426	PCS		4/9			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0003676	PMID:23274426	PCS					C	HPO:skoehler[2013-01-21];HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0003621	PMID:23274426	PCS		2/9			C	HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0000100	PMID:23274426	PCS					P	HPO:skoehler[2013-01-21];HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0000793	PMID:23274426	PCS		9/9			P	HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0005575	OMIM:615008	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:615008	Nephrotic syndrome, type 7		HP:0003593	PMID:23274426	PCS		1/9			C	HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0003073	PMID:23274426	PCS					P	HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0031266	PMID:23274426	PCS					P	HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0000093	PMID:23274426	PCS		9/9			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0001919	OMIM:615008	TAS					P	HPO:skoehler[2013-07-30]
OMIM:615008	Nephrotic syndrome, type 7		HP:0025708	PMID:23274426	PCS		1/9			C	HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0011463	PMID:23274426	PCS		5/9			C	HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0001878	OMIM:615008	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:615008	Nephrotic syndrome, type 7		HP:0000007	PMID:23274426	PCS					I	HPO:skoehler[2013-01-21];HPO:probinson[2023-05-08]
OMIM:615008	Nephrotic syndrome, type 7		HP:0001873	OMIM:615008	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:615008	Nephrotic syndrome, type 7		HP:0004722	PMID:23274426	PCS					P	HPO:skoehler[2013-01-21];HPO:probinson[2023-05-08]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0002960	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0005523	OMIM:614470	TAS					P	HPO:probinson[2013-01-09]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0001442	PMID:21079152	PCS					I	HPO:probinson[2020-07-20]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0002240	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0010702	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0001909	OMIM:614470	TAS					P	HPO:probinson[2013-08-10]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0012311	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0002719	OMIM:614470	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0002729	OMIM:614470	TAS					P	HPO:probinson[2013-08-10]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0001878	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0100827	OMIM:614470	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0001973	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0002205	OMIM:614470	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0002665	OMIM:614470	TAS					P	HPO:probinson[2013-08-10]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0001744	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0001876	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0002731	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0000006	OMIM:614470	TAS					I	HPO:skoehler[2015-12-30]
OMIM:614470	RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic		HP:0001875	OMIM:614470	TAS					P	HPO:skoehler[2015-01-04]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0000486	PMID:19372089	PCS		3/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0001156	PMID:19372089	PCS		3/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0001250	PMID:19372089	PCS		2/18			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0001252	PMID:19372089	PCS		9/18			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0008050	PMID:19372089	PCS		7/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0000708	PMID:19372089	PCS		10/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0003829	PMID:19898479	PCS		50%			I	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0001328	PMID:19372089	PCS		7/25			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0001999	PMID:19372089	PCS		HP:0040282			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0000316	PMID:19372089	PCS		3/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0030680	PMID:19372089	PCS		3/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0004209	PMID:19372089	PCS		4/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0000664	PMID:19372089	PCS		3/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0000377	PMID:19372089	PCS		6/19			P	HPO:iea[2010-11-18]
OMIM:612001	Chromosome 15q13.3 microdeletion syndrome		HP:0000006	OMIM:612001	TAS					I	HPO:iea[2010-11-18]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0003621	PMID:25728773	PCS		4/11			C	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0001332	PMID:25728773	PCS		8/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0003124	PMID:25728773	PCS		5/9			P	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0001272	PMID:25728773	PCS		11/11			P	HPO:skoehler[2015-05-31]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0002495	PMID:25728773	PCS		8/11			P	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0001284	PMID:25728773	PCS		11/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0001251	PMID:25728773	PCS		11/11			P	HPO:skoehler[2015-05-31]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0003073	PMID:25728773	PCS		6/9			P	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0100543	PMID:25728773	PCS		7/10			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0011463	PMID:25728773	PCS		7/11			C	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0006254	PMID:25728773	PCS		5/9			P	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0000657	PMID:25728773	PCS		11/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0009830	PMID:25728773	PCS		11/11			P	HPO:skoehler[2015-05-31]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0007256	PMID:25728773	PCS		2/11			P	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0007366	PMID:25728773	PCS		3/11			P	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0000007	PMID:25728773	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0001513	PMID:25728773	PCS		4/11			P	HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0002445	PMID:25728773	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-02]
OMIM:616267	Ataxia-oculomotor apraxia 4		HP:0003678	PMID:25728773	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-02]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0003730	PMID:18337100	PCS					P	HPO:probinson[2012-04-27];HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0003621	PMID:18337100	PCS					C	HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0003552	PMID:18337100	PCS		7/9			P	HPO:probinson[2012-04-27]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0003740	PMID:18337100	PCS		9/9			P	HPO:probinson[2012-04-27]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0002486	PMID:18337100	PCS		7/9			P	HPO:probinson[2012-04-27];HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0012899	PMID:18337100	PCS		5/9			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0010548	PMID:18337100	PCS		4/9			P	HPO:probinson[2012-04-27]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0025708	PMID:18337100	PCS					C	HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0011463	PMID:18337100	PCS					C	HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0003712	PMID:18337100	PCS		7/9			P	HPO:probinson[2012-04-27];HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0001324	PMID:18337100	PCS		0/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0025605	PMID:18337100	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0000006	PMID:18337100	PCS					I	HPO:probinson[2012-04-27];HPO:probinson[2022-07-19]
OMIM:160800	Myotonia congenita, autosomal dominant		HP:0003326	PMID:18337100	PCS		1/9			P	HPO:probinson[2012-04-27];HPO:probinson[2022-07-19]
OMIM:158810	Bethlem myopathy 1A		HP:0003115	PMID:30808312	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001374	PMID:17886299	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0003236	OMIM:158810	TAS				HP:0012825	P	HPO:probinson[2012-06-04]
OMIM:158810	Bethlem myopathy 1A		HP:0003198	OMIM:158810	IEA					P	HPO:iea[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0100490	OMIM:158810	TAS					P	HPO:probinson[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0003551	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0002460	PMID:30808312;PMID:17886299	PCS		3/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-07-24];ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0012548	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0033685	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0012587	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0011463	PMID:30808312	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0003701	PMID:30808312;PMID:17886299	PCS		4/4			P	HPO:skoehler[2010-06-20];ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001249	PMID:30808312	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0003202	OMIM:158810	TAS					P	HPO:skoehler[2017-07-13]
OMIM:158810	Bethlem myopathy 1A		HP:0003687	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0000010	PMID:30808312	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0000093	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0031910	PMID:30808312	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0002829	PMID:30808312	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0034671	PMID:17886299	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0000007	OMIM:158810	TAS					I	HPO:skoehler[2012-10-17]
OMIM:158810	Bethlem myopathy 1A		HP:0002747	OMIM:158810	IEA					P	HPO:iea[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0003713	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0000006	PMID:17886299	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0034391	PMID:17886299	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0003677	PMID:30808312	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001270	PMID:30808312	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0034677	PMID:30808312;PMID:17886299	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0034681	PMID:17886299	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0009046	PMID:30808312;PMID:17886299	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001626	OMIM:158810	IEA					P	HPO:iea[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0003327	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0007502	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0003724	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0005988	OMIM:158810	IEA					P	HPO:iea[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0003325	OMIM:158810	IEA					P	HPO:iea[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0000473	OMIM:158810	TAS	HP:0003577				P	HPO:skoehler[2013-11-28]
OMIM:158810	Bethlem myopathy 1A		HP:0002650	PMID:17886299	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001761	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001284	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0008180	PMID:30808312;PMID:17886299	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0032152	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0002808	PMID:17886299	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0002804	PMID:17886299	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001558	PMID:30808312	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0001319	OMIM:158810	IEA					P	HPO:iea[2009-02-17]
OMIM:158810	Bethlem myopathy 1A		HP:0000988	PMID:30808312	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0030051	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0040129	PMID:30808312	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0008944	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0003458	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:158810	Bethlem myopathy 1A		HP:0000467	PMID:30808312	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-24]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000121	PMID:17522105	IEA		2/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0002003	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001355	OMIM:611087	IEA					P	HPO:skoehler[2015-12-30]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000486	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0002540	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001250	OMIM:611087	TAS				HP:0031375	P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001252	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001290	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0012371	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000316	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0002119	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000873	PMID:17522105	IEA		2/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000256	PMID:17522105	IEA		15/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000179	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000215	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001249	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001622	PMID:17522105	IEA		15/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000154	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000297	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001561	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000431	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001344	OMIM:611087	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000276	PMID:17522105	IEA		16/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001288	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0011968	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000194	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001382	OMIM:611087	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001263	PMID:17522105	IEA					P	HPO:probinson[2013-01-09]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0000007	PMID:17522105	IEA					I	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001533	OMIM:611087	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0001631	PMID:17522105	IEA		4/16			P	HPO:probinson[2013-04-01]
OMIM:611087	Polyhydramnios, megalencephaly, and symptomatic epilepsy		HP:0002446	OMIM:611087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:142690	Acne inversa, familial		HP:0040154	OMIM:142690	IEA					P	HPO:skoehler[2015-08-05]
OMIM:142690	Acne inversa, familial		HP:0000987	OMIM:142690	IEA					P	HPO:iea[2009-02-17]
OMIM:142690	Acne inversa, familial		HP:0000006	OMIM:142690	IEA					I	HPO:iea[2009-02-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000341	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002982	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002983	OMIM:613848	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0006528	OMIM:613848	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0008905	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002761	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000023	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0004322	OMIM:613848	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0005257	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002021	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0005474	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0003097	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0001290	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0004482	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0010502	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000938	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0011220	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002857	OMIM:613848	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0006532	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000774	OMIM:613848	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002953	OMIM:613848	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0001620	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002753	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002650	OMIM:613848	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0001382	OMIM:613848	TAS				HP:0012837	P	HPO:skoehler[2013-06-06]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002098	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000592	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000272	OMIM:613848	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0011800	OMIM:613848	TAS					P	HPO:skoehler[2013-11-28]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0032988	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0034197	PMID:20188343	PCS		1/1			C	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0003819	PMID:20188343	PCS		1/1			C	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000926	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000007	PMID:20188343	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000348	OMIM:613848	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0006640	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0006487	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000703	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000586	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000883	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0002943	PMID:20188343	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000347	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000787	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000325	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613848	Osteogenesis imperfecta, type X		HP:0000885	PMID:20188343	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:613690	Cardiomyopathy, familial hypertrophic, 7		HP:0001716	PMID:9241277	PCS		3/6			P	HPO:probinson[2022-07-04]
OMIM:613690	Cardiomyopathy, familial hypertrophic, 7		HP:0001639	PMID:11815426	PCS		2/2			P	HPO:probinson[2022-07-04]
OMIM:613690	Cardiomyopathy, familial hypertrophic, 7		HP:0003581	PMID:11815426	IEA		6/6			C	HPO:probinson[2022-07-04]
OMIM:613690	Cardiomyopathy, familial hypertrophic, 7		HP:0005110	OMIM:613690	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613690	Cardiomyopathy, familial hypertrophic, 7		HP:0031992	PMID:9241277	PCS		3/6			P	HPO:probinson[2022-07-04]
OMIM:613690	Cardiomyopathy, familial hypertrophic, 7		HP:0001714	OMIM:613690	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613690	Cardiomyopathy, familial hypertrophic, 7		HP:0000006	PMID:9241277	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0000010	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0032139	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0041070	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0033050	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0041059	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0012476	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0002719	PMID:22035880	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0032132	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0000007	PMID:22035880	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0001945	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0002205	PMID:22035880	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0001744	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0002720	PMID:22035880	TAS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0003326	PMID:22035880	PCS		1/1			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:614699	Immunodeficiency, common variable, 7		HP:0002028	PMID:22035880	PCS		1/1			P	HPO:skoehler[2013-05-29];HPO:probinson[2021-05-09]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000044	OMIM:614841	TAS					P	HPO:probinson[2013-02-23]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000054	PMID:19535795	PCS			MALE		P	HPO:skoehler[2014-11-26]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000013	OMIM:614841	TAS					P	HPO:probinson[2017-05-29]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0040171	OMIM:614841	TAS					P	HPO:probinson[2017-05-29]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0030339	OMIM:614841	TAS					P	HPO:probinson[2017-05-29]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000458	OMIM:614841	TAS		HP:0040282			P	HPO:probinson[2013-02-23]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000007	PMID:19535795	PCS					I	HPO:skoehler[2015-12-30]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000823	OMIM:614841	TAS					P	HPO:probinson[2013-02-23]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0008214	OMIM:614841	TAS					P	HPO:probinson[2017-05-29]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0008734	OMIM:614841	TAS			MALE		P	HPO:skoehler[2014-11-26]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0002555	PMID:19535795	PCS					P	HPO:probinson[2017-05-29]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000028	OMIM:614841	TAS			MALE		P	HPO:skoehler[2014-11-26]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0008724	OMIM:614841	TAS					P	HPO:probinson[2017-05-29]
OMIM:614841	Hypogonadotropic hypogonadism 12 with or without anosmia		HP:0000786	OMIM:614841	TAS			FEMALE		P	HPO:skoehler[2014-11-26]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0011969	PMID:33963445	PCS		1/7			P	HPO:probinson[2022-06-15]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0003251	PMID:33963445	PCS		7/7			P	HPO:probinson[2022-06-15]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0011462	PMID:33963445	PCS		7/7			C	HPO:probinson[2022-06-15]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0008232	PMID:33963445	PCS		5/7			P	HPO:probinson[2022-06-15]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0040171	PMID:33963445	PCS		3/7			P	HPO:probinson[2022-06-15]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0040086	PMID:33963445	PCS		0/7			P	HPO:probinson[2022-06-15]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0001417	PMID:33963445	PCS					I	HPO:probinson[2022-06-15]
OMIM:301077	Spermatogenic failure, X-linked, 4		HP:0000027	PMID:33963445	PCS		5/7			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000286	PMID:16691587	PCS		3/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0001770	PMID:16691587	PCS		2/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000463	OMIM:146390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0001552	PMID:16691587	PCS		2/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0001332	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0004322	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0001252	PMID:16691587	PCS		6/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000316	PMID:16691587	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000338	PMID:16691587	PCS		3/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0009466	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0002812	PMID:16691587	PCS		1/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000218	PMID:16691587	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0008734	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0003745	OMIM:146390	IEA					I	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0006610	PMID:16691587	PCS		2/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0005989	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000311	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000457	PMID:16691587	PCS		6/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0001249	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000358	PMID:16691587	PCS		2/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000054	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000692	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000750	PMID:16691587	PCS		6/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000431	PMID:16691587	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000133	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0001263	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000470	PMID:16691587	PCS		3/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0001518	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000508	PMID:16691587	PCS		5/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0004209	PMID:16691587	PCS		2/7			P	HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000400	PMID:16691587	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000006	PMID:16691587	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-30]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000028	OMIM:146390	IEA					P	HPO:iea[2009-02-17]
OMIM:146390	Chromosome 18p deletion syndrome		HP:0000347	PMID:16691587	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-30]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0008936	PMID:28132689	PCS		1/6			P	HPO:lccarmody[2018-09-10];HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0001276	OMIM:617384	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0002136	OMIM:617384	IEA					P	HPO:skoehler[2017-07-13]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0000750	PMID:28132689	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0001300	PMID:28132689	PCS		1/6			P	HPO:lccarmody[2018-09-10];HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0002067	OMIM:617384	IEA					P	HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0001332	PMID:28132689	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0001263	PMID:28132689	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0001290	OMIM:617384	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0010553	PMID:28132689	PCS		1/6			P	HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0000639	PMID:28132689	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0002509	PMID:28132689	PCS		1/6			P	HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0000007	PMID:28132689	PCS					I	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-09-10]
OMIM:617384	Hyperphenylalaninemia, MILD, non-bh4-deficient		HP:0007018	PMID:28132689	PCS		1/5			P	HPO:lccarmody[2018-09-10]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0003477	PMID:31332438	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001771	PMID:31332438	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0003236	PMID:33206935	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0003551	PMID:33578420	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001252	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002460	PMID:33578420	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0010522	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0034337	PMID:33578420	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0007083	PMID:33578420	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0011463	PMID:31332438	PCS		3/11			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0011462	PMID:31332438	PCS		4/11			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0007002	PMID:33206935;PMID:31332438;PMID:33578420	PCS		9/9			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0009027	PMID:31332438	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0100807	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0012391	PMID:31332438	PCS		3/12			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001763	PMID:31332438	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001765	PMID:31332438	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0000098	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002312	PMID:31332438	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0003487	PMID:33578420	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001382	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0003484	PMID:31332438	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0033383	PMID:33578420	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0009053	PMID:31332438	PCS		11/11			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0000768	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002505	PMID:31332438	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0000006	PMID:31332438	PCS					I	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0025406	PMID:31332438	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0033748	PMID:31332438	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0000189	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0003376	PMID:31332438	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001270	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0012452	PMID:31332438	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001822	PMID:31332438	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002317	PMID:31332438	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0000218	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002359	PMID:31332438	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0009129	PMID:31332438	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002136	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0003621	PMID:33206935;PMID:31332438;PMID:33578420	PCS		6/13			C	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0000750	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001288	PMID:31332438	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0001761	PMID:31332438;PMID:33578420	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002495	PMID:31332438	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0012046	PMID:33578420	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0009830	PMID:33206935	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002522	PMID:31332438	PCS		3/7			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0002600	PMID:31332438	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620528	Neuronopathy, distal hereditary motor, autosomal dominant 11		HP:0008944	PMID:31332438;PMID:33578420	PCS		8/8			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:154780	Marshall syndrome		HP:0000286	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0006407	OMIM:154780	TAS					P	HPO:probinson[2013-04-09]
OMIM:154780	Marshall syndrome		HP:0000343	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000541	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000463	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0004322	PMID:9529347	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0002684	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0003196	PMID:9529347	PCS		9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0003031	OMIM:154780	TAS					P	HPO:skoehler[2010-06-20]
OMIM:154780	Marshall syndrome		HP:0100250	OMIM:154780	TAS					P	HPO:probinson[2012-07-26]
OMIM:154780	Marshall syndrome		HP:0006095	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000518	PMID:9529347	PCS		9/9			P	HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0000316	OMIM:154780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:154780	Marshall syndrome		HP:0006456	OMIM:154780	TAS					P	HPO:probinson[2013-04-09]
OMIM:154780	Marshall syndrome		HP:0000675	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000179	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000215	OMIM:154780	TAS					P	HPO:probinson[2012-07-26]
OMIM:154780	Marshall syndrome		HP:0000175	PMID:9529347	PCS		4/9			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0002673	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000193	PMID:9529347	PCS		4/9			P	HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0005462	PMID:9529347	PCS					P	HPO:probinson[2012-07-26];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0000272	OMIM:154780	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0012019	OMIM:154780	TAS					P	HPO:probinson[2012-07-26]
OMIM:154780	Marshall syndrome		HP:0011800	PMID:9529347	PCS		9/9			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0005086	PMID:9529347	PCS	HP:0003596				P	HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0005280	PMID:9529347	PCS		9/9			P	HPO:probinson[2012-07-26];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0040025	PMID:9529347	PCS		2/9			P	HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0025707	PMID:9529347	PCS					P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0000946	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0006361	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000407	PMID:9529347	PCS	HP:0011463	9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0012283	OMIM:154780	TAS					P	HPO:probinson[2013-04-09]
OMIM:154780	Marshall syndrome		HP:0012284	OMIM:154780	TAS					P	HPO:probinson[2013-04-09]
OMIM:154780	Marshall syndrome		HP:0000926	PMID:9529347	PCS		1/9		HP:0012825	P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0007773	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000403	PMID:9529347	PCS		4/9			P	HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0004209	PMID:9529347	PCS		2/9			P	HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0000565	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0002986	OMIM:154780	TAS					P	HPO:skoehler[2010-06-20]
OMIM:154780	Marshall syndrome		HP:0000201	PMID:9529347	PCS		4/9			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0000006	PMID:9529347	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0000501	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000369	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000347	OMIM:154780	TAS					P	HPO:probinson[2009-02-17]
OMIM:154780	Marshall syndrome		HP:0000545	PMID:9529347	PCS		9/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-23]
OMIM:154780	Marshall syndrome		HP:0002688	PMID:9529347	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-23]
OMIM:615593	Immunodeficiency 16		HP:0003621	OMIM:615593	TAS					C	HPO:skoehler[2017-07-13]
OMIM:615593	Immunodeficiency 16		HP:0100726	PMID:20156905	PCS	HP:0011463	3/3			P	HPO:probinson[2015-03-28]
OMIM:615593	Immunodeficiency 16		HP:0000007	PMID:23897980	PCS					I	HPO:probinson[2015-03-28]
OMIM:615593	Immunodeficiency 16		HP:0001744	PMID:20156905	PCS					P	HPO:probinson[2015-03-28]
OMIM:615593	Immunodeficiency 16		HP:0001876	PMID:20156905	PCS					P	HPO:probinson[2015-03-28]
OMIM:615593	Immunodeficiency 16		HP:0004844	PMID:20156905	PCS					P	HPO:probinson[2015-03-28]
OMIM:615593	Immunodeficiency 16		HP:0002721	OMIM:615593	IEA					P	HPO:skoehler[2015-07-29]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000286	PMID:17220215	PCS		1/4			P	HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0011917	PMID:15706485	PCS		3/3			P	HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0003577	PMID:17220215	PCS		2/4			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000189	OMIM:613684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0001212	PMID:15706485	PCS		2/3			P	HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000486	PMID:17220215;PMID:29506490	PCS		7/11			P	HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0004322	PMID:17220215	PCS		3/4			P	HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000160	PMID:29506490	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0003593	PMID:17220215	PCS		2/4			C	HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0001290	OMIM:613684	IEA					P	HPO:skoehler[2019-02-22]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0010105	PMID:15706485	PCS		3/3			P	HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0010055	PMID:15706485;PMID:29506490	PCS		8/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0100602	OMIM:613684	TAS		HP:0040283			H	HPO:skoehler[2017-07-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0011087	PMID:17220215;PMID:29506490	PCS		2/10			P	HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000678	PMID:29506490	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000218	PMID:29506490	PCS		6/8			P	HPO:skoehler[2012-10-17]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0009765	PMID:17220215;PMID:29506490	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-07-05];HPO:probinson[2022-10-13];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000752	PMID:17220215	PCS		2/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0003745	OMIM:613684	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000278	PMID:17220215	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0001007	PMID:29506490	PCS		3/9			P	HPO:skoehler[2019-04-18]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0001249	PMID:29506490	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000358	PMID:17220215;PMID:29506490	PCS		7/12			P	HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0002553	PMID:15706485	PCS		3/3			P	HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000670	PMID:17220215	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000494	PMID:17220215;PMID:15706485;PMID:29506490	PCS		11/15			P	HPO:probinson[2022-10-13];HPO:skoehler[2019-02-22];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000252	PMID:17220215;PMID:29506490	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000750	PMID:17220215;PMID:29506490	PCS		5/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0002650	PMID:29506490	PCS		0/9			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000574	PMID:17220215;PMID:29506490	PCS		8/12			P	ORCID:0000-0002-0736-9199[2024-07-05];HPO:probinson[2022-10-13];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0011968	PMID:17220215;PMID:29506490	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-05];HPO:probinson[2022-10-13];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0001263	PMID:29506490	PCS		4/7			P	HPO:skoehler[2012-10-17]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0002194	OMIM:613684	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0011304	PMID:15706485;PMID:29506490	PCS		11/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0011094	OMIM:613684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000729	PMID:29506490	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000448	PMID:17220215;PMID:29506490	PCS		10/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000689	PMID:17220215;PMID:29506490	PCS		5/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000527	PMID:17220215;PMID:29506490	PCS		9/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0008523	OMIM:613684	TAS					P	HPO:probinson[2017-05-25]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000444	PMID:17220215	PCS		1/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0001159	OMIM:613684	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000006	PMID:15706485	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000589	PMID:29506490	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0002566	OMIM:613684	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000369	PMID:29506490	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:613684	Rubinstein-Taybi syndrome 2		HP:0000347	PMID:29506490	PCS		2/9			P	HPO:skoehler[2012-10-17]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003555	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003236	PMID:27040688	PCS		3/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003676	OMIM:616924	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0002021	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003198	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003474	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003390	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0007141	OMIM:616924	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0007340	PMID:27040688	PCS		4/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003828	OMIM:616924	TAS					M	HPO:skoehler[2017-07-13]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003805	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0002936	OMIM:616924	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0002515	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003701	OMIM:616924	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0002359	OMIM:616924	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0009129	PMID:27040688	PCS		3/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0001265	OMIM:616924	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003445	PMID:27040688	PCS		4/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003200	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003487	PMID:27040688	PCS		4/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0001761	OMIM:616924	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003484	PMID:27040688	PCS		3/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0002495	PMID:27040688	PCS		2/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0007210	PMID:27040688	PCS		4/4			P	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0000006	PMID:27040688	PCS					I	HPO:probinson[2017-06-25]
OMIM:616924	Charcot-Marie-Tooth disease, axonal, type 2CC		HP:0003557	PMID:27040688	PCS					P	HPO:probinson[2017-06-25]
OMIM:150280	LARYNGOMALACIA		HP:0004886	OMIM:150280	TAS					P	HPO:skoehler[2015-05-23]
OMIM:150280	LARYNGOMALACIA		HP:0002098	OMIM:150280	TAS					P	HPO:probinson[2009-02-17]
OMIM:150280	LARYNGOMALACIA		HP:0002778	OMIM:150280	TAS					P	HPO:probinson[2015-05-23]
OMIM:150280	LARYNGOMALACIA		HP:0000006	OMIM:150280	TAS					I	HPO:probinson[2009-02-17]
OMIM:150280	LARYNGOMALACIA		HP:0001601	OMIM:150280	TAS					P	HPO:probinson[2009-02-17]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002421	PMID:30787422	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002069	PMID:36576126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002100	PMID:38083972;PMID:36576126	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000486	PMID:38083972	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002188	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002540	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0004322	PMID:38083972;PMID:36576126	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001250	PMID:38083972;PMID:36576126	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001272	PMID:36576126	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001252	PMID:30787422	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001251	PMID:36576126	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0012389	PMID:38083972	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0033725	PMID:30787422;PMID:38083972	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0007281	PMID:36576126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000639	PMID:38083972;PMID:36576126	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001508	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0011463	PMID:38083972	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0100702	PMID:36576126	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000316	PMID:30787422;PMID:38083972	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0025336	PMID:38083972	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001348	PMID:30787422	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001249	PMID:30787422	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0008936	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000252	PMID:30787422;PMID:38083972	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002059	PMID:36576126	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000750	PMID:38083972	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0025373	PMID:30787422;PMID:36576126	PCS		5/6			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001344	PMID:30787422;PMID:36576126	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0031936	PMID:38083972	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0003487	PMID:30787422	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002079	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002197	PMID:30787422	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0003121	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002572	PMID:36576126	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001263	PMID:38083972	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0002273	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0001141	PMID:36576126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0005484	PMID:36576126	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0033454	PMID:38083972;PMID:36576126	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0034353	PMID:38083972;PMID:36576126	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0011451	PMID:36576126	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000007	PMID:28097321	PCS					I	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000648	PMID:38083972;PMID:36576126	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000543	PMID:36576126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000248	PMID:38083972	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000347	PMID:30787422;PMID:38083972	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:621150	Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language		HP:0000369	PMID:36576126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-14]
OMIM:607829	Mitral valve prolapse, myxomatous 2		HP:0001653	OMIM:607829	IEA					P	HPO:iea[2009-02-17]
OMIM:607829	Mitral valve prolapse, myxomatous 2		HP:0000006	OMIM:607829	IEA					I	HPO:iea[2009-02-17]
OMIM:607829	Mitral valve prolapse, myxomatous 2		HP:0001634	OMIM:607829	IEA					P	HPO:iea[2009-02-17]
OMIM:607829	Mitral valve prolapse, myxomatous 2		HP:0003831	OMIM:607829	IEA					I	HPO:iea[2009-02-17]
OMIM:611093	Intellectual developmental disorder, autosomal recessive 7		HP:0000252	PMID:18452889	PCS		0/7			P	HPO:probinson[2022-06-14]
OMIM:611093	Intellectual developmental disorder, autosomal recessive 7		HP:0011463	PMID:18455129	PCS		2/2			C	HPO:probinson[2022-06-14]
OMIM:611093	Intellectual developmental disorder, autosomal recessive 7		HP:0001263	PMID:18455129	PCS		2/2			P	HPO:probinson[2022-06-14]
OMIM:611093	Intellectual developmental disorder, autosomal recessive 7		HP:0000007	PMID:18452889	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-06-14]
OMIM:611093	Intellectual developmental disorder, autosomal recessive 7		HP:0001249	PMID:18452889	PCS		7/7			P	HPO:probinson[2013-04-01];HPO:probinson[2022-06-14]
OMIM:613874	Cardiomyopathy, familial hypertrophic, 18		HP:0003596	PMID:12705874	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:613874	Cardiomyopathy, familial hypertrophic, 18		HP:0001639	PMID:12705874	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613874	Cardiomyopathy, familial hypertrophic, 18		HP:0005110	OMIM:613874	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613874	Cardiomyopathy, familial hypertrophic, 18		HP:0001712	PMID:12705874	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613874	Cardiomyopathy, familial hypertrophic, 18		HP:0100749	OMIM:613874	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613874	Cardiomyopathy, familial hypertrophic, 18		HP:0004757	PMID:12705874	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613874	Cardiomyopathy, familial hypertrophic, 18		HP:0000006	PMID:12705874	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:300433	Intellectual developmental disorder, X-linked 81		HP:0001419	OMIM:300433	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300433	Intellectual developmental disorder, X-linked 81		HP:0001249	OMIM:300433	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000486	PMID:16596670	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0010648	PMID:15731757;PMID:16928994	PCS		11/34			P	HPO:iea[2010-02-23];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0410151	PMID:23608731	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0010646	PMID:16928994	PCS		7/30			P	HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0012432	PMID:16596670	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0002616	PMID:29706644;PMID:15731757;PMID:16596670;PMID:16928994;PMID:31475485	PCS		39/40			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001647	PMID:29706644;PMID:15731757;PMID:16596670;PMID:31475485	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000316	PMID:15731757;PMID:16596670;PMID:16928994	PCS		31/37			P	HPO:probinson[2021-05-23];HPO:probinson[2024-03-29];HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0004959	PMID:29706644;PMID:15731757;PMID:16596670;PMID:31475485	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000238	PMID:15731757;PMID:16928994	PCS		6/34			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001643	PMID:15731757	PCS	HP:0003623	2/4			P	HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001643	PMID:16928994	PCS	HP:0003623	10/30			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001643	PMID:31475485	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001763	PMID:16596670	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000278	PMID:29706644;PMID:15731757;PMID:16596670;PMID:16928994;PMID:31475485	PCS		19/39			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001249	PMID:16928994	PCS					P	HPO:iea[2009-02-17]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000175	PMID:29706644;PMID:15731757;PMID:16596670;PMID:31475485	PCS		2/9			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000494	PMID:16596670	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0002870	PMID:16596670	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001382	PMID:15731757;PMID:16596670;PMID:16928994	PCS		25/37			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001263	PMID:29706644;PMID:15731757;PMID:16928994	PCS		4/36			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001065	PMID:29706644	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0005182	PMID:29706644;PMID:15731757;PMID:16596670;PMID:31475485	PCS		0/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0030745	PMID:15731757	PCS		0/3			P	HPO:probinson[2021-10-21]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0012385	PMID:15731757;PMID:16928994;PMID:31475485	PCS		12/36			P	HPO:skoehler[2013-10-22];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0100259	PMID:29706644;PMID:15731757	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0100775	PMID:31475485	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0002308	PMID:15731757;PMID:16928994	PCS		4/34			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000767	PMID:29706644	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000766	PMID:15731757;PMID:16928994	PCS		24/35			P	HPO:iea[2010-02-23];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000768	PMID:29706644;PMID:15731757;PMID:16596670	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0005815	PMID:16596670	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000520	PMID:15731757;PMID:16596670;PMID:16928994	PCS		6/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000006	PMID:16928994	PCS					I	HPO:iea[2009-02-17]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000369	PMID:16596670;PMID:31475485	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000324	PMID:16596670	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0005116	PMID:29706644;PMID:15731757;PMID:16928994	PCS		16/35			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0003577	PMID:16596670	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000023	PMID:16596670	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0009004	PMID:16596670	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0004937	PMID:29706644;PMID:15731757;PMID:16596670;PMID:31475485	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000218	PMID:29706644;PMID:16596670;PMID:31475485	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000977	PMID:15731757;PMID:16596670;PMID:16928994	PCS		12/35			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000411	PMID:16596670;PMID:31475485	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0004933	PMID:29706644;PMID:16596670;PMID:16928994;PMID:31475485	PCS		6/14			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000577	PMID:15731757	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001166	PMID:15731757;PMID:16596670;PMID:16928994	PCS		25/36			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001363	PMID:15731757;PMID:16596670;PMID:16928994;PMID:31475485	PCS		18/37			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0003302	PMID:16596670	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0002650	PMID:29706644;PMID:15731757;PMID:16596670;PMID:16928994	PCS		21/38			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001762	PMID:15731757;PMID:16928994	PCS		16/35			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001162	PMID:16928994	PCS					P	HPO:iea[2009-02-17]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000193	PMID:15731757;PMID:16928994;PMID:31475485	PCS		30/34			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0003581	PMID:31475485	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000592	PMID:15731757;PMID:16596670;PMID:16928994	PCS		14/36			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000272	PMID:15731757;PMID:16596670;PMID:16928994;PMID:31475485	PCS		23/38			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0034720	PMID:29706644;PMID:15731757	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001083	PMID:29706644;PMID:16596670;PMID:16928994	PCS		0/32			P	HPO:probinson[2018-06-26];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001519	PMID:15731757;PMID:16928994	PCS		7/35			P	HPO:iea[2010-02-23];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000508	PMID:16596670	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001631	PMID:15731757	PCS	HP:0003577	1/3			P	HPO:probinson[2021-05-23];HPO:probinson[2024-03-29]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001631	PMID:16928994	PCS		5/30			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001631	PMID:29706644	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001631	PMID:16596670	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001631	PMID:31475485	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0004944	OMIM:609192	IEA					P	HPO:iea[2009-02-17]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0000347	PMID:16596670;PMID:16928994;PMID:31475485	PCS		11/13			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:609192	Loeys-Dietz syndrome 1		HP:0001634	PMID:29706644;PMID:15731757;PMID:16596670;PMID:31475485	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:600808	Enuresis, nocturnal, 2		HP:0000006	OMIM:600808	IEA					I	HPO:iea[2009-02-17]
OMIM:600808	Enuresis, nocturnal, 2		HP:0010677	OMIM:600808	TAS					P	HPO:skoehler[2009-02-17]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0033605	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002583	PMID:33782605	PCS		4/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0003593	PMID:33782605	PCS		3/3			C	HPO:probinson[2022-08-15]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0003073	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0012191	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0003228	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0001369	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0040218	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0001386	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002110	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0200029	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0001581	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0005263	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0012387	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0032132	PMID:33782605	PCS		5/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002749	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0000403	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0000006	PMID:33782605	TAS					I	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0005218	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002588	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002027	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0033628	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0004464	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:6000257	PMID:33782605	PCS		1/6			P	HPO:probinson[2024-02-09]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002041	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002719	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0001903	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002716	PMID:33782605	PCS		3/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0001824	PMID:33782605	PCS		3/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0001744	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002039	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002754	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002850	PMID:33782605	PCS		4/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002014	PMID:33782605	PCS		5/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0005403	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002013	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0000155	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0100280	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0003460	PMID:33782605	PCS		3/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002090	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0010976	PMID:33782605	PCS		2/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0012115	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0011227	PMID:33782605	PCS		3/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0031381	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0011473	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002729	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0009797	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0001954	PMID:33782605	PCS		3/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0000988	PMID:33782605	PCS		3/6			P	HPO:probinson[2021-08-16]
OMIM:619381	Immunodeficiency 82 with systemic inflammation		HP:0002722	PMID:33782605	PCS		1/6			P	HPO:probinson[2021-08-16]
OMIM:620500	Spermatogenic failure 87		HP:0003251	PMID:37004249	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:620500	Spermatogenic failure 87		HP:0011462	PMID:37004249	PCS		2/2			C	HPO:probinson[2024-02-11]
OMIM:620500	Spermatogenic failure 87		HP:0000007	PMID:37004249	PCS					I	HPO:probinson[2024-02-11]
OMIM:620500	Spermatogenic failure 87		HP:6000501	PMID:37004249	PCS		2/2			P	HPO:probinson[2024-04-04]
OMIM:300355	Intellectual developmental disorder, X-linked 73		HP:0001419	OMIM:300355	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300355	Intellectual developmental disorder, X-linked 73		HP:0001417	OMIM:300355	IEA					I	HPO:skoehler[2013-01-11]
OMIM:300355	Intellectual developmental disorder, X-linked 73		HP:0000664	OMIM:300355	TAS					P	HPO:skoehler[2017-07-13]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000286	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000341	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000187	OMIM:314320	TAS					P	HPO:probinson[2022-02-01]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000431	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000023	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0004443	OMIM:314320	TAS					P	HPO:probinson[2013-03-11]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0004322	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000243	PMID:30797980	IEA		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-13]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0004442	OMIM:314320	TAS					P	HPO:probinson[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0001250	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0001263	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0005494	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0001629	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0001518	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0001419	PMID:30797980	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-01-13]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000601	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0004209	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000218	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000444	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0001249	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000369	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000358	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:314320	Trigonocephaly with short stature and developmental delay		HP:0000237	OMIM:314320	IEA					P	HPO:iea[2009-02-17]
OMIM:614869	Usher syndrome, type IJ		HP:0003577	OMIM:614869	TAS					C	HPO:skoehler[2012-11-16]
OMIM:614869	Usher syndrome, type IJ		HP:0001751	OMIM:614869	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614869	Usher syndrome, type IJ		HP:0000007	OMIM:614869	TAS					I	HPO:skoehler[2012-11-16]
OMIM:614869	Usher syndrome, type IJ		HP:0001270	OMIM:614869	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614869	Usher syndrome, type IJ		HP:0000510	OMIM:614869	TAS					P	HPO:skoehler[2012-11-16]
OMIM:242600	IMINOGLYCINURIA		HP:0003137	OMIM:242600	IEA					P	HPO:iea[2009-02-17]
OMIM:242600	IMINOGLYCINURIA		HP:0000007	OMIM:242600	IEA					I	HPO:iea[2009-02-17]
OMIM:242600	IMINOGLYCINURIA		HP:0003080	OMIM:242600	IEA					P	HPO:iea[2009-02-17]
OMIM:242600	IMINOGLYCINURIA		HP:0003108	OMIM:242600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:242600	IMINOGLYCINURIA		HP:0001249	OMIM:242600	IEA					P	HPO:iea[2009-02-17]
OMIM:242600	IMINOGLYCINURIA		HP:0000478	OMIM:242600	IEA					P	HPO:iea[2009-02-17]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0003565	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0005421	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0030783	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0003493	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0025289	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0031364	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0045042	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0032436	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0011463	PMID:37422272	PCS		1/1			C	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0001903	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0034751	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0033178	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0000967	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0000421	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0000006	PMID:37422272	PCS					I	HPO:probinson[2024-03-10]
OMIM:620514	Immune dysregulation, autoimmunity, and autoinflammation		HP:0000225	PMID:37422272	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0002840	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0002202	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0000100	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0004322	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0012203	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0002719	PMID:30361506	PCS					P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0001888	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0002716	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0012390	PMID:30361506	PCS		2/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0001945	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0006532	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0009789	PMID:30361506	PCS		2/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0001744	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0025615	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0003203	PMID:30361506	PCS		3/3			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0000155	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0100280	PMID:30361506	PCS		4/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0100279	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0032252	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0011110	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0001735	PMID:30361506	PCS		2/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0001878	PMID:30312704	PCS		1/1			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0000007	PMID:30361506	PCS					I	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0000964	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0002923	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31];HPO:probinson[2020-10-12]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0002206	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:618935	Chronic granulomatous disease 5, autosomal recessive		HP:0001433	PMID:30361506	PCS		1/8			P	HPO:probinson[2020-08-31]
OMIM:613860	Immunodeficiency due to ficolin 3 deficiency		HP:0002783	PMID:19535802	PCS					P	HPO:probinson[2013-02-23]
OMIM:613860	Immunodeficiency due to ficolin 3 deficiency		HP:0033165	PMID:20971976	PCS	HP:0003623	2/2			P	HPO:probinson[2020-10-13]
OMIM:613860	Immunodeficiency due to ficolin 3 deficiency		HP:0002726	PMID:20971976	PCS		1/2			P	HPO:probinson[2020-10-13]
OMIM:613860	Immunodeficiency due to ficolin 3 deficiency		HP:0000007	PMID:19535802	PCS					I	HPO:probinson[2013-01-09]
OMIM:613860	Immunodeficiency due to ficolin 3 deficiency		HP:0002722	PMID:19535802	PCS					P	HPO:probinson[2013-02-23]
OMIM:613860	Immunodeficiency due to ficolin 3 deficiency		HP:0200043	PMID:19535802	PCS					P	HPO:probinson[2013-02-23]
OMIM:246300	Leprosy, susceptibility to		HP:0002715	OMIM:246300	IEA					P	HPO:iea[2009-02-17]
OMIM:246300	Leprosy, susceptibility to		HP:0000006	OMIM:246300	TAS					I	HPO:skoehler[2012-10-17]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0006009	PMID:22652534	PCS		1/1			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0004325	OMIM:615222	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0006429	PMID:22652534	PCS		1/1		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0001377	PMID:22652534	PCS		4/4			P	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0001552	OMIM:615222	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0003311	PMID:22652534	PCS		1/1		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0004322	PMID:22652534	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0010049	PMID:22652534	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0000280	PMID:22652534	PCS		0/4			P	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0003071	PMID:22652534	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0012428	PMID:22652534	PCS		1/4			P	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0010743	PMID:22652534	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0011463	PMID:22652534	PCS		4/4			C	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0003307	PMID:22652534	PCS		4/4			P	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0002857	PMID:22652534	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0001763	PMID:22652534	PCS		1/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0001249	PMID:22652534	PCS		0/4			P	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0009803	PMID:22652534	PCS		1/1			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0008812	PMID:22652534	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0003521	OMIM:615222	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0001783	PMID:22652534	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0003025	PMID:22652534	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0000470	PMID:22652534	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0003180	PMID:22652534	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0000926	PMID:22652534	PCS		1/1			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0000007	PMID:22652534	PCS					I	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0000768	PMID:22652534	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0006247	PMID:22652534	PCS		4/4			P	HPO:probinson[2023-02-09]
OMIM:615222	Smith-Mccort dysplasia 2		HP:0000303	PMID:22652534	PCS		0/4			P	HPO:probinson[2023-02-09]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001133	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000286	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001531	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001252	PMID:27633801;PMID:29232904	PCS		3/3			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0003593	PMID:27633801	IEA		2/2			C	HPO:probinson[2022-04-24]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000639	PMID:29232904;PMID:30304524	PCS		7/8			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0100806	PMID:30304524	PCS		3/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0007401	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002611	PMID:30304524	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000252	PMID:30304524	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002474	PMID:30304524	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002155	PMID:27633801	PCS		2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002079	PMID:27633801	PCS		2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000293	PMID:27633801	PCS		2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002197	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001382	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000490	PMID:27633801;PMID:30304524	PCS		9/9			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002151	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002194	PMID:30304524	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0033454	PMID:29232904;PMID:30304524	PCS		8/8			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001738	PMID:30304524	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000007	PMID:27633801	PCS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001414	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001397	PMID:27633801;PMID:29232904	PCS		2/3			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000662	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001274	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001394	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002240	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0030319	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001508	PMID:27633801;PMID:29232904	PCS		2/3			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001629	PMID:30304524	PCS		1/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001903	PMID:30304524	PCS		3/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001943	PMID:30304524	PCS		5/7		HP:0012828	P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002716	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0005948	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001748	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002119	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001747	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000218	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0006577	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0006579	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001744	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001622	PMID:30304524	IEA	HP:0003577	3/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0008619	PMID:30304524	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000431	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0002013	PMID:27633801	PCS		2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0012715	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0005280	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0011232	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000308	PMID:27633801	PCS		1/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001998	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0001510	PMID:30304524	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619418	Infantile-onset multisystem neurologic, endocrine, and pancreatic disease 2		HP:0000786	PMID:29232904	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001396	PMID:15521008	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001036	OMIM:607626	IEA					P	HPO:iea[2009-02-17]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001399	PMID:15521008	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001596	PMID:15521008	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001395	PMID:15521008	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0030991	PMID:15521008	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0002240	PMID:15521008	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0040162	OMIM:607626	TAS					P	HPO:skoehler[2015-06-22]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0045075	PMID:15521008	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0008070	OMIM:607626	IEA					P	HPO:iea[2009-02-17]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001409	PMID:15521008	PCS		3/4			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0000958	OMIM:607626	IEA					P	HPO:iea[2009-02-17]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001408	PMID:15521008	PCS		2/3			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0006297	PMID:15521008	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0000653	PMID:15521008	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001744	PMID:15521008	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0000677	PMID:15521008	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0000952	PMID:15521008	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0001249	PMID:15521008	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0003623	PMID:15521008	PCS		4/4			C	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0005248	PMID:15521008	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0025092	OMIM:607626	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0100874	OMIM:607626	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0008064	PMID:15521008	PCS		4/4			P	HPO:probinson[2013-12-15];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0000668	PMID:15521008	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0000007	PMID:15521008	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607626	Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis		HP:0000989	PMID:15521008	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001276	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002067	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001773	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001332	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002340	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001272	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002384	PMID:26740508	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001250	OMIM:617435	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0003593	PMID:26740508	PCS		1/1			C	HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0000733	PMID:26740508	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002317	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0000713	PMID:26740508	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0006855	PMID:26740508	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001347	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0008936	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0003763	OMIM:617435	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002059	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002015	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001344	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002650	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002376	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0011968	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001263	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0011448	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0002808	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0007256	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0000007	PMID:26740508	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-20]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0200055	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001257	OMIM:617435	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0000545	OMIM:617435	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617435	Lopes-Maciel-Rodan syndrome		HP:0001337	PMID:26740508	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000486	PMID:29656859	PCS		6/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000540	PMID:29656859	PCS		2/13			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001250	PMID:29656859	PCS		9/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0003298	PMID:29656859	PCS	HP:0003577	1/16			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001251	PMID:29656859	PCS		4/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001290	PMID:29656859	PCS		7/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001270	PMID:29656859	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000639	PMID:29656859	PCS		1/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0012450	PMID:29656859	PCS		1/16			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0012076	PMID:29656859	PCS		1/16			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000657	PMID:29656859	PCS		1/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001249	PMID:29656859	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0002311	PMID:29656859	PCS		2/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0006879	PMID:29656859	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000750	PMID:29656859	PCS		10/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0002079	PMID:29656859	PCS		1/9			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0025097	PMID:29656859	PCS		1/16			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001321	PMID:29656859	PCS		2/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0031936	PMID:29656859	PCS	HP:0003593	8/12			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001263	PMID:29656859	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000729	PMID:29656859	PCS		5/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000646	PMID:29656859	PCS		1/13			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0007256	PMID:29656859	PCS		1/16			P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000565	PMID:29656859	PCS		2/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0001337	PMID:29656859	PCS		8/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000028	PMID:29656859	PCS		1/8	MALE		P	HPO:probinson[2020-08-08]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000006	PMID:29656859	PCS					I	HPO:probinson[2019-02-14]
OMIM:618060	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia		HP:0000126	PMID:29656859	PCS		1/16			P	HPO:probinson[2020-08-08]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0002344	PMID:15773042	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0003477	PMID:29995202	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0001265	PMID:15773042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0001276	PMID:29995202;PMID:15773042	PCS		2/2			P	HPO:probinson[2021-09-22];HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0002871	PMID:15773042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0011968	PMID:29995202	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0002283	PMID:15773042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0003593	PMID:15773042	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0002093	PMID:15773042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0031358	PMID:15773042	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0032792	PMID:29995202	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0030890	PMID:29995202	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0007266	PMID:15773042	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0000007	PMID:15773042	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0002119	PMID:29995202	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0002878	PMID:15773042	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0002922	PMID:29995202;PMID:15773042	PCS		2/2			P	HPO:probinson[2021-09-22];HPO:iea[2009-02-17];HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0001522	PMID:15773042	PCS		1/1			C	HPO:probinson[2021-09-22]
OMIM:611722	Krabbe disease, atypical, due to saposin A deficiency		HP:0001347	PMID:29995202	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0002521	PMID:24056535	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0000750	PMID:24056535	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0000486	PMID:24056535	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0001250	PMID:24056535	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0011342	PMID:24056535	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0003593	PMID:24056535	PCS		1/1			C	HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0011153	PMID:24056535	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0032388	PMID:24056535	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0000006	PMID:24056535	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-07]
OMIM:615544	Periventricular nodular heterotopia 6		HP:0012469	PMID:24056535	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000286	PMID:10958759	PCS					P	HPO:probinson[2018-01-25]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0008935	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000494	OMIM:614882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0001250	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0011968	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0002240	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0001284	OMIM:614882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0001290	OMIM:614882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0011344	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0010655	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000518	OMIM:614882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000316	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000448	OMIM:614882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000007	OMIM:614882	TAS					I	HPO:probinson[2013-01-09]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000348	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000337	OMIM:614882	TAS					P	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0001558	OMIM:614882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000218	OMIM:614882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0001522	OMIM:614882	TAS					C	HPO:probinson[2013-02-24]
OMIM:614882	Peroxisome biogenesis disorder 10A (Zellweger)		HP:0000347	OMIM:614882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002487	PMID:21112253	PCS		6/11			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0001276	PMID:19478460	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0003676	PMID:19478460	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002067	PMID:21112253	PCS		10/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0001332	PMID:21112253	PCS	HP:0003593	6/11			P	HPO:probinson[2022-04-09];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002063	PMID:21112253	PCS		10/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002020	PMID:21112253	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0003593	PMID:21112253	PCS		8/11			C	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002062	OMIM:613135	IEA					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0012048	PMID:21112253	PCS		11/11			P	HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0034201	PMID:19478460	PCS	HP:0003593	3/3			P	HPO:probinson[2022-04-15]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0000338	PMID:21112253	PCS		11/11			P	HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002019	PMID:21112253	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0003623	PMID:21112253	PCS		3/11			C	HPO:probinson[2022-04-09];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0008936	PMID:21112253	PCS		8/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0001300	PMID:21112253	PCS	HP:0003593	6/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0011968	PMID:21112253	PCS		6/11			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002451	OMIM:613135	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002396	PMID:21112253	PCS		4/11			P	HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0001263	PMID:19478460	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002072	PMID:21112253	PCS		5/11			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0002194	PMID:21112253	PCS		9/9			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0010553	PMID:21112253	PCS		2/11			P	HPO:probinson[2022-04-09];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0100660	PMID:21112253	PCS		5/11			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0031931	PMID:21112253	PCS		8/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0007256	PMID:21112253	PCS	HP:0003593	7/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0000007	PMID:19478460	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-04-09]
OMIM:613135	Parkinsonism-Dystonia, infantile, 1		HP:0001337	PMID:21112253	PCS		8/11			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-04-09]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0001199	PMID:23812780	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-01]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0003577	PMID:23812780	PCS		1/1			C	HPO:probinson[2023-03-01]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0001629	PMID:23812780	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0030270	PMID:23812780	PCS		1/1			P	HPO:probinson[2015-01-31]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0001896	PMID:23812780	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0001972	PMID:23812780	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0001895	PMID:23812780	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615550	Diamond-Blackfan anemia 12		HP:0000006	PMID:23812780	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-01]
OMIM:614896	Sinoatrial node dysfunction and deafness		HP:0003577	PMID:21131953	PCS		6/6			C	HPO:probinson[2022-07-02]
OMIM:614896	Sinoatrial node dysfunction and deafness		HP:0000365	PMID:21131953	PCS	HP:0003577	6/6			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-07-02]
OMIM:614896	Sinoatrial node dysfunction and deafness		HP:0001662	PMID:21131953	PCS		6/6			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-07-02]
OMIM:614896	Sinoatrial node dysfunction and deafness		HP:0000007	PMID:21131953	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-07-02]
OMIM:614896	Sinoatrial node dysfunction and deafness		HP:0031862	PMID:21131953	PCS		6/6			P	HPO:probinson[2022-07-02]
OMIM:614896	Sinoatrial node dysfunction and deafness		HP:0025074	PMID:21131953	PCS		0/6			P	HPO:probinson[2022-07-02]
OMIM:614896	Sinoatrial node dysfunction and deafness		HP:0001279	PMID:21131953	PCS		2/6			P	HPO:probinson[2022-07-02]
OMIM:133900	Hemifacial hyperplasia		HP:0000327	OMIM:133900	IEA					P	HPO:iea[2009-02-17]
OMIM:133900	Hemifacial hyperplasia		HP:0000689	OMIM:133900	IEA					P	HPO:iea[2009-02-17]
OMIM:133900	Hemifacial hyperplasia		HP:0000006	OMIM:133900	IEA					I	HPO:iea[2009-02-17]
OMIM:133900	Hemifacial hyperplasia		HP:0000324	OMIM:133900	IEA					P	HPO:iea[2009-02-17]
OMIM:618074	Epilepsy, familial adult myoclonic, 6		HP:0033054	PMID:29507423	PCS					P	HPO:probinson[2020-12-01]
OMIM:618074	Epilepsy, familial adult myoclonic, 6		HP:0003581	PMID:29507423	PCS					C	HPO:probinson[2020-12-01]
OMIM:618074	Epilepsy, familial adult myoclonic, 6		HP:0000006	PMID:29507423	PCS					I	HPO:probinson[2020-12-01];HPO:probinson[2022-12-03]
OMIM:616059	Mirror movements 3		HP:0001696	PMID:25098561	PCS		0/3			P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-12]
OMIM:616059	Mirror movements 3		HP:0000007	PMID:25098561	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616059	Mirror movements 3		HP:0001335	PMID:25098561	PCS					P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-12]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0003577	PMID:15877279	PCS		1/5			C	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0002202	PMID:15877279	PCS		2/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0003198	OMIM:261740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001250	PMID:15877279	PCS		1/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0034532	PMID:15877279	PCS		5/5			P	HPO:probinson[2023-03-31]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0033568	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0012398	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0000518	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0012250	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0012251	PMID:15877279	PCS		2/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0000238	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0012050	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0002615	PMID:15877279	PCS		2/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0000158	PMID:15877279	PCS		2/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0006677	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001623	PMID:15877279	PCS		2/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001663	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001541	PMID:15877279	PCS		1/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001662	PMID:15877279	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001640	PMID:15877279	PCS		3/5			P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0011968	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0002098	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0200128	PMID:15877279	PCS		1/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0005165	PMID:15877279	PCS		2/5			P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0010851	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0010872	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0100598	PMID:15877279	PCS		1/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0034197	PMID:15877279	PCS		1/5			C	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001639	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001635	PMID:15877279	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001998	OMIM:261740	IEA					P	HPO:iea[2009-02-17]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001638	PMID:15877279	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0000961	OMIM:261740	IEA					P	HPO:iea[2009-02-17]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0001698	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0002104	PMID:15877279	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0000006	PMID:15877279	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-23]
OMIM:261740	Glycogen storage disease of heart, lethal congenital		HP:0000105	PMID:15877279	PCS		2/5			P	HPO:probinson[2023-01-23]
OMIM:614128	Lactate dehydrogenase B deficiency		HP:0045041	PMID:2334429	PCS					P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-10]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0003676	PMID:24833714	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0003596	PMID:24833714	PCS		1/2			C	HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0001310	PMID:24833714	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0000020	PMID:24833714	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0002064	OMIM:613647	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0030891	PMID:24833714	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0003593	PMID:24833714	PCS		1/2			C	HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0001251	OMIM:613647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0002061	OMIM:613647	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0033725	PMID:24833714	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0007340	OMIM:613647	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0001268	OMIM:613647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0002313	PMID:24833714	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0001249	OMIM:613647	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0002136	PMID:24833714	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0001300	OMIM:613647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0002079	OMIM:613647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0001263	PMID:24833714	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0009830	OMIM:613647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0030890	PMID:24833714	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0000007	PMID:20613862	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0030051	PMID:24833714	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0001258	PMID:24833714	PCS		2/2			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-11]
OMIM:613647	Spastic paraplegia 48, autosomal recessive		HP:0000488	OMIM:613647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615236	Woods syndrome		HP:0011939	PMID:1640433	PCS		2/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0001377	PMID:1640433	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0000233	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0000431	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0011937	PMID:1640433	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0001263	PMID:1640433	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0011335	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0031008	PMID:1640433	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0001629	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0000954	PMID:1640433	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0000648	PMID:1640433	PCS		2/2			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0009765	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0001258	PMID:1640433	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0002558	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0001249	PMID:1640433	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0001821	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:615236	Woods syndrome		HP:0001347	PMID:1640433	PCS		1/3			P	HPO:probinson[2021-07-13]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0002169	PMID:23365102	PCS		12/12			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0010804	PMID:23365102	PCS		7/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0003236	PMID:23365102	PCS		10/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0010628	PMID:23365102	PCS		2/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0002240	PMID:32453731	PCS		4/4			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001290	PMID:32453731	PCS		4/4			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0030718	PMID:32453731	PCS		1/1			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0031295	PMID:32453731	PCS		1/1			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001723	PMID:23365102	PCS		2/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001522	PMID:23365102	PCS		13/13			C	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001644	PMID:23365102	PCS		7/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0003623	PMID:23365102;PMID:32453731	PCS		17/17			C	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0003324	PMID:23365102	PCS	HP:0003623	13/13		HP:0003676	P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0031318	PMID:23365102;PMID:32453731	PCS		11/11			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0030149	PMID:32453731	PCS		2/4			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001685	PMID:32453731	PCS		1/1			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0200128	PMID:32453731	PCS		1/1			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0011664	PMID:23365102	PCS		2/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001639	PMID:23365102	PCS		6/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0000508	PMID:23365102	PCS		1/13			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0000007	PMID:23365102	PCS					I	HPO:probinson[2021-10-11];HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0006543	PMID:32453731	PCS	HP:0003623	2/4			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001653	PMID:32453731	PCS		2/4			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0001337	PMID:23365102	PCS		12/12			P	HPO:probinson[2021-10-11]
OMIM:619424	Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy		HP:0003755	PMID:23365102	PCS		13/13			P	HPO:probinson[2021-10-11]
OMIM:609637	Holoprosencephaly 5		HP:0006988	PMID:19955556	PCS	HP:0003577	27/83			P	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000341	PMID:19955556	PCS		14/30			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0003577	PMID:11479728;PMID:30855487	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0000340	PMID:19955556	PCS		2/30			P	HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000582	PMID:19955556	PCS		29/30			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000463	PMID:19955556	PCS		22/30			P	HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0002002	PMID:19955556	PCS		14/30			P	HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000243	OMIM:609637	TAS					P	PATOC:GVG[2012-04-24]; PATOC:PS[2012-04-24]
OMIM:609637	Holoprosencephaly 5		HP:0001272	PMID:30855487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0001250	PMID:19955556	PCS					P	HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0100702	PMID:30855487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0011461	PMID:32695376	PCS		1/1			C	HPO:probinson[2022-02-05]
OMIM:609637	Holoprosencephaly 5		HP:0000316	OMIM:609637	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0006870	PMID:19955556	PCS	HP:0003577	10/83			P	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000337	PMID:19955556	PCS		2/30			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000238	PMID:19955556;PMID:30855487	PCS		12/94			P	PATOC:GVG[2012-04-24]; PATOC:PS[2012-04-24];HPO:probinson[2020-09-13];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0002119	PMID:30855487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0000218	PMID:19955556	PCS		12/69			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0001249	OMIM:609637	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609637	Holoprosencephaly 5		HP:0001347	PMID:30855487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0032549	PMID:30855487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0006956	PMID:32695376	PCS		1/1			P	HPO:probinson[2022-02-05]
OMIM:609637	Holoprosencephaly 5		HP:0000252	OMIM:609637;PMID:11479728	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-05-11];PATOC:GVG[2012-04-24]; PATOC:PS[2012-04-24]
OMIM:609637	Holoprosencephaly 5		HP:0025670	PMID:32695376	PCS		1/1			P	HPO:probinson[2022-02-05]
OMIM:609637	Holoprosencephaly 5		HP:0001360	PMID:19955556	PCS					P	PATOC:GVG[2012-04-24]; PATOC:PS[2012-04-24];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0001263	PMID:30855487	PCS		1/1			P	PATOC:GVG[2012-04-24]; PATOC:PS[2012-04-24];HPO:probinson[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0005280	PMID:19955556;PMID:11479728	PCS		11/31			P	ORCID:0000-0002-0736-9199[2024-05-11];HPO:skoehler[2012-11-18];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0012385	PMID:11479728	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0000348	PMID:19955556	PCS		5/30			P	HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000601	OMIM:609637	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0002507	PMID:19955556	PCS	HP:0003577	42/83			P	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0002507	PMID:11479728	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0002507	PMID:30855487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0000400	PMID:19955556	PCS		12/30			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000202	PMID:19955556	PCS		7/69			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000664	PMID:19955556	PCS		4/30			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000520	PMID:11479728	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:609637	Holoprosencephaly 5		HP:0000006	PMID:19955556	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-13]
OMIM:609637	Holoprosencephaly 5		HP:0000863	PMID:19955556	PCS					P	HPO:probinson[2020-09-13]
OMIM:108000	Arteries, anomalies of		HP:0001626	OMIM:108000	IEA					P	HPO:iea[2009-02-17]
OMIM:108000	Arteries, anomalies of		HP:0000006	OMIM:108000	IEA					I	HPO:iea[2009-02-17]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0001265	OMIM:600175	TAS					P	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0003577	PMID:20037588	PCS		20/20			C	HPO:probinson[2022-11-23]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0003236	OMIM:600175	TAS				HP:0012825	P	HPO:probinson[2018-03-07]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0002650	PMID:20037588	PCS		12/20			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-11-23]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0001762	OMIM:600175	IEA					P	HPO:iea[2018-03-07]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0003693	OMIM:600175	TAS					P	HPO:probinson[2018-03-07]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0003273	OMIM:600175	TAS					P	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0003680	OMIM:600175	TAS					C	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0001284	PMID:20037588	PCS		20/20			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-11-23]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0002460	OMIM:600175	TAS					P	HPO:probinson[2018-03-07]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0006380	OMIM:600175	TAS					P	HPO:probinson[2018-03-07]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0009053	PMID:20037588	PCS		20/20			P	HPO:probinson[2022-11-23]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0002808	OMIM:600175	TAS					P	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0003829	OMIM:600175	TAS					I	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0002804	PMID:20037588	PCS		15/20			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-11-23]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0001558	OMIM:600175	TAS					P	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0003307	OMIM:600175	TAS					P	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0007269	OMIM:600175	TAS					P	HPO:probinson[2018-03-07]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0002987	OMIM:600175	TAS					P	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0008964	OMIM:600175	IEA					P	HPO:iea[2018-03-07]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0001763	OMIM:600175	TAS					P	HPO:skoehler[2012-11-25]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0000006	PMID:20037588	PCS					I	HPO:iea[2018-03-07];HPO:probinson[2022-11-23]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0008956	PMID:20037588	PCS		0/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:600175	Neuronopathy, distal hereditary motor, type VIII		HP:0008944	PMID:20037588	PCS		20/20			P	HPO:probinson[2022-11-23]
OMIM:193220	Vitreoretinochoroidopathy		HP:0030666	OMIM:193220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:193220	Vitreoretinochoroidopathy		HP:0007902	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000662	OMIM:193220	PCS					P	HPO:probinson[2012-04-06]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000541	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000486	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000551	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000482	PMID:15452077	PCS	HP:0003577				P	HPO:probinson[2012-04-07];HPO:probinson[2022-11-07]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000580	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:193220	Vitreoretinochoroidopathy		HP:0030856	PMID:15452077	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000639	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:193220	Vitreoretinochoroidopathy		HP:0008043	OMIM:193220	PCS					P	HPO:probinson[2012-04-06]
OMIM:193220	Vitreoretinochoroidopathy		HP:0010693	OMIM:193220	PCS					P	HPO:probinson[2012-04-07]
OMIM:193220	Vitreoretinochoroidopathy		HP:0007661	OMIM:193220	IEA					P	HPO:iea[2012-04-06]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000618	OMIM:193220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000519	PMID:15452077	PCS	HP:0003577				P	HPO:probinson[2022-11-07]
OMIM:193220	Vitreoretinochoroidopathy		HP:0007641	OMIM:193220	PCS		HP:0040283			P	HPO:probinson[2012-04-07]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000568	PMID:15452077	PCS	HP:0003577	HP:0040283			P	HPO:probinson[2012-04-07];HPO:probinson[2022-11-07]
OMIM:193220	Vitreoretinochoroidopathy		HP:0007985	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000006	PMID:15452077	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-07]
OMIM:193220	Vitreoretinochoroidopathy		HP:0000501	OMIM:193220	IEA					P	HPO:iea[2009-02-17]
OMIM:617409	Diamond-Blackfan anemia 17		HP:0001903	PMID:25424902	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617409	Diamond-Blackfan anemia 17		HP:0000953	PMID:25424902	PCS					P	HP:probinson[2018-05-13]
OMIM:617409	Diamond-Blackfan anemia 17		HP:0000006	PMID:25424902	PCS					I	HPO:skoehler[2017-07-13]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0001166	OMIM:614100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0002827	OMIM:614100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0002097	OMIM:614100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0030680	OMIM:614100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0001627	OMIM:614100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0000776	OMIM:614100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0000006	OMIM:614100	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614100	Cutis laxa, neonatal, with marfanoid phenotype		HP:0000973	OMIM:614100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:145100	Hyperpigmentation of eyelids		HP:0007406	OMIM:145100	IEA					P	HPO:iea[2009-02-17]
OMIM:145100	Hyperpigmentation of eyelids		HP:0000006	OMIM:145100	IEA					I	HPO:iea[2009-02-17]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0003202	PMID:24119684	PCS		1/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0001562	PMID:24119684	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0003577	PMID:24119684	PCS		2/2			C	HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0000750	PMID:24119684	PCS		2/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0001310	PMID:24119684	PCS		1/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0002151	PMID:24119684	PCS		2/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0001252	PMID:24119684	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0010862	PMID:24119684	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0011923	PMID:24119684	PCS		2/2			P	HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0040014	PMID:24119684	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0012120	PMID:24119684	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0009046	PMID:24119684	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0000007	PMID:24119684	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0000505	PMID:24119684	PCS		2/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0001511	PMID:24119684	PCS		2/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0001972	PMID:24119684	PCS		1/2			P	HPO:skoehler[2014-02-25]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0001337	PMID:24119684	PCS		1/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0003128	PMID:24119684	PCS		2/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-03-18]
OMIM:615578	Combined oxidative phosphorylation deficiency 18		HP:0004821	PMID:24119684	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0001199	OMIM:141400	TAS					P	HPO:probinson[2009-02-17]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0000384	OMIM:141400	TAS					P	HPO:probinson[2012-03-31]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0004467	OMIM:141400	TAS					P	HPO:probinson[2012-03-31]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0000175	OMIM:141400	TAS					P	HPO:probinson[2012-03-31]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0100335	OMIM:141400	TAS					P	HPO:probinson[2012-03-31]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0011332	OMIM:141400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0008551	OMIM:141400	TAS					P	HPO:probinson[2012-03-31]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0000405	OMIM:141400	TAS					P	HPO:probinson[2009-02-17]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0003778	OMIM:141400	TAS					P	HPO:probinson[2009-02-17]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0000202	OMIM:141400	TAS					P	HPO:probinson[2012-07-27]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0009943	OMIM:141400	TAS					P	HPO:probinson[2009-02-17]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0000006	OMIM:141400	TAS					I	HPO:probinson[2009-02-17]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0000413	OMIM:141400	TAS					P	HPO:probinson[2009-02-17]
OMIM:141400	Hemifacial microsomia with radial defects		HP:0000324	OMIM:141400	TAS					P	HPO:probinson[2009-02-17]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0003577	PMID:26524591	PCS		1/1			C	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0001156	OMIM:618048	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0001250	PMID:29805043	PCS		1/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0003493	PMID:26524591;PMID:29805043	PCS		3/3			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0030374	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0001508	OMIM:618048	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0002718	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0002716	OMIM:618048	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0009125	PMID:26524591	PCS		1/1			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0030084	OMIM:618048	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0001945	PMID:26524591	PCS		1/1		HP:0031796	P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0003623	PMID:29805043	IEA		2/2			C	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0003565	PMID:26524591	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0025379	PMID:29805043	PCS		1/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0410243	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0001482	PMID:26524591	PCS		1/1			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0032069	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0003261	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0031234	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0010976	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0011227	PMID:26524591	PCS		1/1			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0002829	PMID:26524591	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0100539	OMIM:618048	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0034156	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0033221	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0000988	PMID:29805043	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0004429	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0001873	PMID:29805043	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0000006	PMID:26524591	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0025528	PMID:26524591	PCS		1/1			P	HPO:probinson[2022-04-19]
OMIM:618048	Proteasome-Associated autoinflammatory syndrome 2		HP:0003237	PMID:29805043	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:272700	TAURODONTISM		HP:0000679	OMIM:272700	IEA					P	HPO:iea[2009-02-17]
OMIM:272700	TAURODONTISM		HP:0000007	OMIM:272700	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0002069	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0002421	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0003577	PMID:33386993	PCS		2/2			C	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000463	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000160	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0003196	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000280	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0012553	PMID:33386993	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0001804	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0008398	PMID:33386993	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0009882	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0001800	PMID:33386993	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0005707	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000696	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0004379	PMID:33386993	PCS		0/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000252	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0001344	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000194	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0001263	PMID:33386993	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000691	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0200105	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0031061	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0012168	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000826	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000007	PMID:33386993	PCS					I	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0001857	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0001631	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619356	Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome		HP:0000347	PMID:33386993	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:614672	Cardiomyopathy, dilated, 2B		HP:0003596	PMID:21965549	PCS		2/2			C	HPO:probinson[2022-07-03]
OMIM:614672	Cardiomyopathy, dilated, 2B		HP:0005110	PMID:21965549	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-03]
OMIM:614672	Cardiomyopathy, dilated, 2B		HP:0001635	PMID:21965549	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:614672	Cardiomyopathy, dilated, 2B		HP:0000007	PMID:21965549	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:614672	Cardiomyopathy, dilated, 2B		HP:0012664	PMID:21965549	PCS		2/2			P	HPO:probinson[2022-07-03]
OMIM:614672	Cardiomyopathy, dilated, 2B		HP:0001644	PMID:21965549	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000286	PMID:12116237;PMID:24259107;PMID:21552266	PCS		5/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000365	PMID:12116237;PMID:21552266	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0004322	PMID:12116237;PMID:21552266	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0002101	PMID:21552266	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000160	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0003196	PMID:24259107	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001252	PMID:21552266	PCS		1/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0012745	PMID:21552266	PCS		1/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000957	PMID:21552266	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0011220	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000954	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001249	PMID:12116237	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000252	PMID:21552266	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000494	PMID:24259107	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0002750	PMID:12116237	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000490	PMID:24259107;PMID:21552266	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0032569	PMID:21552266	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000601	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000007	PMID:21552266	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0004209	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001659	PMID:12116237	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000325	PMID:24259107	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0008846	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000369	PMID:12116237;PMID:24259107	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0008905	PMID:12116237;PMID:24259107;PMID:21552266	PCS		3/6			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000581	PMID:24259107	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0008070	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0200040	PMID:12116237;PMID:21552266	PCS		2/5			P	HPO:skoehler[2014-02-06];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001629	PMID:12116237;PMID:21552266	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000414	PMID:12116237	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0030084	PMID:21552266	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001682	PMID:12116237;PMID:21552266	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001363	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000276	PMID:12116237	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001680	PMID:21552266	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0005280	OMIM:614114	TAS		2/4			P	HPO:skoehler[2012-11-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0010535	PMID:12116237;PMID:21552266	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0100830	PMID:24259107	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001518	PMID:24259107;PMID:21552266	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000821	PMID:12116237;PMID:21552266	PCS		3/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000824	PMID:12116237	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001511	PMID:21552266	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0002007	PMID:24259107	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000268	PMID:24259107	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001510	PMID:12116237;PMID:24259107;PMID:21552266	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0001631	PMID:21552266	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0000347	PMID:12116237;PMID:24259107	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:614114	Mosaic variegated aneuploidy syndrome 2		HP:0002247	PMID:21552266	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-18]
OMIM:276200	T-SUBSTANCE ANOMALY		HP:0001939	OMIM:276200	IEA					P	HPO:iea[2009-02-17]
OMIM:276200	T-SUBSTANCE ANOMALY		HP:0000007	OMIM:276200	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:276200	T-SUBSTANCE ANOMALY		HP:0001510	OMIM:276200	IEA					P	HPO:iea[2009-02-17]
OMIM:276200	T-SUBSTANCE ANOMALY		HP:0001249	OMIM:276200	IEA					P	HPO:iea[2009-02-17]
OMIM:604307	Cataract 2, multiple types		HP:0010926	PMID:10521291	PCS					P	HPO:probinson[2022-10-07]
OMIM:604307	Cataract 2, multiple types		HP:0100018	OMIM:604307	TAS					P	HPO:probinson[2013-02-19]
OMIM:604307	Cataract 2, multiple types		HP:0000639	OMIM:604307	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604307	Cataract 2, multiple types		HP:0000482	OMIM:604307	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:604307	Cataract 2, multiple types		HP:0000519	OMIM:604307	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604307	Cataract 2, multiple types		HP:0000646	OMIM:604307	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604307	Cataract 2, multiple types		HP:0000613	OMIM:604307	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:604307	Cataract 2, multiple types		HP:0010698	PMID:10521291	PCS					P	HPO:probinson[2022-10-07]
OMIM:604307	Cataract 2, multiple types		HP:0000505	OMIM:604307	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604307	Cataract 2, multiple types		HP:0000006	PMID:10521291	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-10-07]
OMIM:605019	Hypobetalipoproteinemia, familial, 2		HP:0003563	PMID:20942659	PCS					P	HPO:probinson[2013-01-09]
OMIM:605019	Hypobetalipoproteinemia, familial, 2		HP:0012153	PMID:20942659	PCS					P	HPO:probinson[2013-02-22]
OMIM:605019	Hypobetalipoproteinemia, familial, 2		HP:0000007	PMID:20942659	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2020-07-15]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0002069	OMIM:605021	TAS					P	HPO:probinson[2009-02-17]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0002123	OMIM:605021	TAS					P	HPO:probinson[2009-02-17]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0002373	OMIM:605021	IEA					P	HPO:iea[2009-02-17]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0031629	PMID:23517570	PCS		2/2			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0001250	PMID:23517570	PCS		4/4			P	HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0001260	PMID:23517570	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0002066	PMID:23517570	PCS		2/4			P	HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0001263	PMID:23517570	PCS		4/4			P	HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0001251	PMID:23517570	PCS		1/4			P	HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0003593	OMIM:605021	TAS		4/4			C	HPO:probinson[2013-12-15];HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0002070	PMID:23517570	PCS		1/4			P	HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0010546	PMID:23517570	PCS		1/4			P	HPO:probinson[2022-11-08]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0000007	OMIM:605021	IEA					I	HPO:iea[2009-02-17]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0007359	OMIM:605021	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605021	Myoclonic epilepsy, familial infantile		HP:0001249	PMID:23517570	PCS		4/4			P	HPO:probinson[2022-11-08]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0000021	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0009806	PMID:7524315	PCS					P	HPO:probinson[2013-12-15];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0004322	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0002013	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0001250	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0001508	PMID:7524315	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0001959	PMID:7524315	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0000737	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0001955	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0000007	PMID:7524315	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0008872	PMID:7524315	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0003228	PMID:7524315	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0000103	PMID:7524315	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0002019	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0000006	OMIM:125800	IEA					I	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0001986	PMID:7524315	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-10]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0001249	OMIM:125800	IEA					P	HPO:iea[2009-02-17]
OMIM:125800	Diabetes insipidus, nephrogenic, 2		HP:0003623	OMIM:125800	IEA					C	HPO:iea[2009-02-17]
OMIM:613643	Parkinson disease 5, susceptibility to		HP:0002067	PMID:9774100	PCS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:613643	Parkinson disease 5, susceptibility to		HP:0002063	PMID:9774100	PCS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:613643	Parkinson disease 5, susceptibility to		HP:0003829	PMID:9774100	IEA					I	HPO:probinson[2020-06-27]
OMIM:613643	Parkinson disease 5, susceptibility to		HP:0002172	PMID:9774100	PCS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:613643	Parkinson disease 5, susceptibility to		HP:0002548	PMID:9774100	PCS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:613643	Parkinson disease 5, susceptibility to		HP:0000006	PMID:9774100	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0004566	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0002023	OMIM:617425;PMID:28148688	PCS		3/12			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0010605	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001250	PMID:28132690	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0001252	PMID:28331220;PMID:28148688	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002063	PMID:28148688	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0003196	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0003593	PMID:28132690;PMID:28331220	PCS		4/11			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000280	PMID:28132690	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0100255	PMID:28132690	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0031545	PMID:28148688	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000639	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0011463	PMID:28132690	PCS		1/9			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0011462	PMID:28132690	PCS		2/9			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002938	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000316	PMID:28132690	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0100806	PMID:28148688	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000954	PMID:28132690	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001888	PMID:28132690	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002812	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001407	PMID:28132690;PMID:28331220;PMID:28148688	PCS		6/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001522	PMID:28132690	PCS		3/9			C	HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0002656	PMID:28132690	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001249	PMID:28132690	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0020206	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0004315	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0003623	PMID:28132690	PCS					C	HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0002751	PMID:28132690	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000253	PMID:28132690	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0001385	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000252	PMID:28132690;PMID:28331220	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002155	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0002673	PMID:28132690	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0004894	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000331	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000293	PMID:28132690	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002197	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0001263	PMID:28132690;PMID:28331220;PMID:28148688	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0003083	PMID:28132690	PCS		4/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000926	PMID:28132690;PMID:28331220;PMID:28148688	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000767	PMID:28132690;PMID:28148688	PCS		3/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000448	PMID:28132690	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000007	PMID:28132690;PMID:28148688	PCS		20/20			I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001019	OMIM:617425	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0005619	PMID:28132690;PMID:28331220;PMID:28148688	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0008445	PMID:28331220;PMID:28148688	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000960	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002943	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001216	PMID:28132690	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0030799	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002169	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0003577	PMID:28132690;PMID:28331220;PMID:28148688	PCS		14/15			C	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0003016	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000582	PMID:28132690;PMID:28148688	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000463	PMID:28331220	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001156	PMID:28132690;PMID:28331220;PMID:28148688	PCS		9/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0003498	PMID:28132690	PCS		6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0003375	OMIM:617425	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0005352	PMID:28132690;PMID:28148688	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001270	PMID:28132690	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0004060	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0003090	PMID:28132690	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0100865	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0001508	PMID:28148688	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0002719	PMID:28132690;PMID:28148688	PCS		4/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0007340	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0008873	PMID:28132690;PMID:28148688	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0025116	PMID:28148688	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0006532	PMID:28331220	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0000455	PMID:28132690	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0006610	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000498	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002676	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0001347	PMID:28148688	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0008936	PMID:28132690	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002850	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002179	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0001363	PMID:28148688	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0004313	PMID:28132690	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0001880	PMID:28132690	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0003621	PMID:28132690	PCS		3/9			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0009826	PMID:28132690;PMID:28331220;PMID:28148688	PCS		6/10			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0001561	PMID:28331220	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0004430	PMID:28132690;PMID:28148688	PCS		7/12			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2022-11-08]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002176	PMID:28331220;PMID:28148688	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0030320	PMID:28148688	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0005562	PMID:28132690	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0005280	PMID:28132690;PMID:28331220	PCS		11/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities		HP:0008462	OMIM:617425	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0034374	PMID:28148688	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0002007	PMID:28331220	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:617425	Immunoskeletal dysplasia with neurodevelopmental abnormalitie		HP:0000347	PMID:28331220;PMID:28148688	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:177820	Pseudo-Von willebrand disease		HP:0003010	OMIM:177820	IEA					P	HPO:iea[2009-02-17]
OMIM:177820	Pseudo-Von willebrand disease		HP:0000006	OMIM:177820	IEA					I	HPO:iea[2009-02-17]
OMIM:177820	Pseudo-Von willebrand disease		HP:0004854	OMIM:177820	IEA					P	HPO:iea[2009-02-17]
OMIM:168900	Patella, chondromalacia of		HP:0003045	OMIM:168900	IEA					P	HPO:skoehler[2009-02-17]
OMIM:168900	Patella, chondromalacia of		HP:0000006	OMIM:168900	IEA					I	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0002014	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0002013	OMIM:606528	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0002909	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0001508	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0002242	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0000007	OMIM:606528	IEA					I	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0001943	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0008872	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0000124	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0000842	OMIM:606528	TAS					P	HPO:probinson[2009-02-17]
OMIM:606528	Homozygous 11p15-p14 deletion syndrome		HP:0008527	OMIM:606528	IEA					P	HPO:iea[2009-02-17]
OMIM:617343	Hyperparathyroidism 4		HP:0000938	PMID:27745835	PCS		3/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:617343	Hyperparathyroidism 4		HP:0006780	PMID:27745835	PCS		1/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:617343	Hyperparathyroidism 4		HP:0008200	PMID:27745835	PCS		19/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:617343	Hyperparathyroidism 4		HP:0003581	PMID:27745835	PCS		19/19			C	HPO:probinson[2023-01-23]
OMIM:617343	Hyperparathyroidism 4		HP:0003072	PMID:27745835	PCS		19/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:617343	Hyperparathyroidism 4		HP:0000006	PMID:27745835	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:617343	Hyperparathyroidism 4		HP:0000787	PMID:27745835	PCS		4/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:615554	Multiple fibroadenomas of the breast		HP:0010619	PMID:18779591	PCS				HP:0030651	P	HP:probinson[2019-03-02]
OMIM:615554	Multiple fibroadenomas of the breast		HP:0000006	PMID:18779591	PCS					I	HPO:skoehler[2014-01-28];HP:probinson[2019-03-02]
OMIM:614892	Immunodeficiency 31A		HP:0003621	PMID:11452125	PCS		1/2			C	HPO:probinson[2023-02-09]
OMIM:614892	Immunodeficiency 31A		HP:0020086	PMID:11452125	PCS		1/2			P	HPO:probinson[2023-02-09]
OMIM:614892	Immunodeficiency 31A		HP:0011463	PMID:11452125	PCS		1/2			C	HPO:probinson[2023-02-09]
OMIM:614892	Immunodeficiency 31A		HP:0011275	PMID:11452125	PCS		1/2			P	HPO:probinson[2023-02-09]
OMIM:614892	Immunodeficiency 31A		HP:0003829	OMIM:614892	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614892	Immunodeficiency 31A		HP:0004429	PMID:11452125	PCS		1/2			P	HPO:probinson[2023-02-09]
OMIM:614892	Immunodeficiency 31A		HP:0012302	OMIM:614892	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614892	Immunodeficiency 31A		HP:0000006	PMID:11452125	PCS					I	HPO:skoehler[2015-08-23];HPO:probinson[2023-02-09]
OMIM:614892	Immunodeficiency 31A		HP:0002721	OMIM:614892	IEA					P	HPO:skoehler[2015-08-23]
OMIM:615540	Deafness, autosomal recessive 76		HP:0003577	PMID:23348741	PCS					C	HPO:probinson[2023-03-12]
OMIM:615540	Deafness, autosomal recessive 76		HP:0000408	PMID:23348741	PCS		6/6			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-03-12]
OMIM:615540	Deafness, autosomal recessive 76		HP:0011463	PMID:23348741	PCS					C	HPO:probinson[2023-03-12]
OMIM:615540	Deafness, autosomal recessive 76		HP:0003593	PMID:23348741	PCS					C	HPO:probinson[2023-03-12]
OMIM:615540	Deafness, autosomal recessive 76		HP:0000007	PMID:23348741	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-12]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0004325	OMIM:614886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0003455	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000286	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0030799	OMIM:614886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0003577	PMID:20683989	PCS		1/1			C	HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001476	OMIM:614886	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001399	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0004322	OMIM:614886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001250	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000260	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001252	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0100806	PMID:20683989	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000238	OMIM:614886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001643	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0002910	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0007305	OMIM:614886	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001348	PMID:20683989	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0003103	OMIM:614886	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0002059	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000252	OMIM:614886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000431	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0010759	PMID:20683989	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0002033	PMID:20683989	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001263	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001081	OMIM:614886	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0009553	OMIM:614886	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0010461	OMIM:614886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001719	OMIM:614886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0002904	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000629	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000448	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000007	PMID:9727033	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001558	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001631	PMID:20683989	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000267	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001510	OMIM:614886	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000124	OMIM:614886	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0000325	PMID:20683989	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-25]
OMIM:614886	Peroxisome biogenesis disorder 12A (Zellweger)		HP:0001612	PMID:20683989	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0000572	OMIM:611726	TAS		HP:0040283			P	HPO:skoehler[2012-12-03]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0003676	OMIM:611726	IEA					C	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0000252	PMID:22748208	PCS		2/2			P	HPO:skoehler[2012-12-03];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0002059	PMID:22748208	PCS		2/2			P	HPO:skoehler[2012-12-03];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0002078	PMID:17455289	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0001344	PMID:22748208	PCS		2/2			P	HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0002123	OMIM:611726	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0002079	PMID:22748208	PCS		1/2			P	HPO:skoehler[2012-12-03];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0002376	PMID:22748208	PCS	HP:0011463	2/2			P	HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0001272	PMID:22748208	PCS		2/2			P	HPO:skoehler[2012-12-03];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0001260	PMID:17455289	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0003593	PMID:22748208	PCS		2/2			C	HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0032794	PMID:17455289	PCS					P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0032667	PMID:17455289	PCS		1/3			P	HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0000007	PMID:17455289	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0003208	OMIM:611726	TAS					P	HPO:skoehler[2012-12-03]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0000648	PMID:22748208	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0007334	PMID:17455289	PCS		2/3			P	HPO:probinson[2021-06-26]
OMIM:611726	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions		HP:0001249	PMID:17455289	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:245180	Kifafa seizure disorder		HP:0001250	OMIM:245180	IEA					P	HPO:iea[2009-02-17]
OMIM:245180	Kifafa seizure disorder		HP:0000007	OMIM:245180	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:245180	Kifafa seizure disorder		HP:0001249	OMIM:245180	IEA					P	HPO:iea[2009-02-17]
OMIM:245180	Kifafa seizure disorder		HP:0006932	OMIM:245180	IEA					P	HPO:iea[2009-02-17]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0003510	PMID:29228025	PCS		2/2			P	HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000275	PMID:29228025	PCS		1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0005832	PMID:29228025	PCS		2/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0004325	PMID:29228025	PCS		2/2			P	HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000054	PMID:29228025	PCS		1/1	MALE		P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000252	PMID:29228025	IEA		2/2			P	HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000494	PMID:29228025	PCS		2/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0002650	PMID:29228025	PCS		1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000540	PMID:29228025	PCS		2/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0011968	PMID:29228025	PCS		1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000160	PMID:29228025	PCS		1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0001263	PMID:29228025	PCS					P	HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0002020	PMID:29228025	PCS		1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0003241	PMID:29228025	PCS					P	HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0001508	PMID:29228025	PCS	HP:0003593	1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0001804	PMID:29228025	PCS		1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0025515	PMID:29228025	PCS		1/1	FEMALE		P	HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000448	PMID:29228025	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000007	PMID:29228025	PCS					I	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0002857	PMID:29228025	PCS		1/2			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000823	PMID:29228025	PCS					P	HPO:probinson[2020-07-21]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0000444	PMID:29228025	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:618702	Short stature and microcephaly with genital anomalies		HP:0001741	PMID:29228025	PCS		1/1	MALE		P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:611040	Microphthalmia, isolated 5		HP:0007737	PMID:17167404	PCS		4/4			P	HPO:probinson[2012-07-26];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0000662	PMID:17167404	PCS		4/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0012426	PMID:17167404	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0011505	PMID:17167404	PCS		0/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0030823	PMID:17167404	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0000518	PMID:17167404	PCS		0/4			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0012152	PMID:17167404	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0011462	PMID:17167404	PCS		4/4			C	HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0008323	PMID:17167404	PCS		4/4			P	HPO:probinson[2012-07-26];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0000613	OMIM:611040	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:611040	Microphthalmia, isolated 5		HP:0008499	PMID:17167404	PCS		4/4			P	HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0000007	PMID:17167404	PCS					I	HPO:probinson[2012-07-26];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0000568	PMID:17167404	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0007663	PMID:17167404	PCS		8/8			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0000543	PMID:17167404	PCS		4/4			P	HPO:probinson[2023-02-17]
OMIM:611040	Microphthalmia, isolated 5		HP:0007722	PMID:17167404	PCS		1/1			P	HPO:probinson[2012-07-26];HPO:probinson[2023-02-17]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0003577	PMID:23160277	PCS		4/4			C	HPO:probinson[2022-07-03]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0001597	PMID:23160277	PCS		0/4			P	HPO:probinson[2022-07-03]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0001162	PMID:23160277	PCS		4/4			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-07-03]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0009374	PMID:23160277	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-03]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0006482	PMID:23160277	PCS		0/4			P	HPO:probinson[2022-07-03]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0000007	PMID:23160277	PCS					I	HPO:skoehler[2013-06-06];HPO:probinson[2022-07-03]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0001830	PMID:23160277	PCS		4/4			P	HPO:probinson[2022-07-03]
OMIM:615226	Polydactyly, postaxial, type A6		HP:0000971	PMID:23160277	PCS		0/4			P	HPO:probinson[2022-07-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0002014	OMIM:261750	TAS					P	HPO:probinson[2009-02-17]
OMIM:261750	Glycogen storage disease type IXb		HP:0004322	PMID:17689125	PCS		3/15			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:6000333	PMID:21634085	PCS					P	HPO:probinson[2024-02-27]
OMIM:261750	Glycogen storage disease type IXb		HP:0001252	PMID:17689125	PCS		2/15			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0002240	PMID:17689125	PCS		10/15			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0003593	PMID:17689125	PCS					C	HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0009051	OMIM:261750	TAS					P	HPO:probinson[2015-04-18]
OMIM:261750	Glycogen storage disease type IXb		HP:0011463	PMID:17689125	PCS					C	HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0000007	PMID:9215682	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0001943	PMID:17689125	PCS		10/15			P	HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0001324	OMIM:261750	TAS		3/15		HP:0012825	P	HPO:probinson[2015-04-18];HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0001510	PMID:17689125	PCS		7/15			P	HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0006568	OMIM:261750	TAS					P	HPO:probinson[2015-04-18]
OMIM:261750	Glycogen storage disease type IXb		HP:0001744	PMID:17689125	PCS		2/15			P	HPO:probinson[2022-12-03]
OMIM:261750	Glycogen storage disease type IXb		HP:0002149	PMID:17689125	PCS		1/5			P	HPO:probinson[2022-12-03]
OMIM:613657	D-2-hydroxyglutaric aciduria 2		HP:0040146	PMID:20847235	PCS		7/7			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:613657	D-2-hydroxyglutaric aciduria 2		HP:0012321	PMID:20847235	PCS		14/14			P	HPO:probinson[2013-08-11];HPO:probinson[2020-07-24]
OMIM:613657	D-2-hydroxyglutaric aciduria 2		HP:0001250	OMIM:613657	TAS					P	HPO:probinson[2013-08-11]
OMIM:613657	D-2-hydroxyglutaric aciduria 2		HP:0001263	OMIM:613657	TAS					P	HPO:probinson[2013-01-09]
OMIM:613657	D-2-hydroxyglutaric aciduria 2		HP:0001252	OMIM:613657	TAS					P	HPO:probinson[2013-08-11]
OMIM:613657	D-2-hydroxyglutaric aciduria 2		HP:0001638	OMIM:613657	TAS					P	HPO:probinson[2013-08-11]
OMIM:613657	D-2-hydroxyglutaric aciduria 2		HP:0000006	PMID:20847235	PCS					I	HPO:probinson[2013-08-11];HPO:probinson[2020-07-24]
OMIM:600165	Nanophthalmos 1		HP:0007633	OMIM:600165	IEA					P	HPO:iea[2009-02-17]
OMIM:600165	Nanophthalmos 1		HP:0000006	OMIM:600165	IEA					I	HPO:iea[2009-02-17]
OMIM:193230	Snowflake vitreoretinal degeneration		HP:0000541	PMID:14644728	PCS		3/14			P	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:193230	Snowflake vitreoretinal degeneration		HP:0000518	PMID:14644728	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-04-30]
OMIM:193230	Snowflake vitreoretinal degeneration		HP:0030663	OMIM:193230	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:193230	Snowflake vitreoretinal degeneration		HP:0011533	PMID:14644728	PCS		4/6			P	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:193230	Snowflake vitreoretinal degeneration		HP:0032027	OMIM:193230	TAS					P	HPO:skoehler[2019-09-07]
OMIM:193230	Snowflake vitreoretinal degeneration		HP:0012038	PMID:14644728	PCS		4/5			P	HPO:probinson[2021-04-30]
OMIM:193230	Snowflake vitreoretinal degeneration		HP:0000006	PMID:18179896	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-04-30]
OMIM:616707	Deafness, autosomal dominant 68		HP:0000407	PMID:25816005	PCS	HP:0003621	10/10			P	HP:probinson[2019-03-02]
OMIM:616707	Deafness, autosomal dominant 68		HP:0000006	PMID:25816005	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0000033	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0001595	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0000054	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0000818	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0032382	OMIM:264600	IEA					I	HPO:skoehler[2019-09-07]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0000051	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0001939	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0001608	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0000007	OMIM:264600	IEA					I	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0000048	OMIM:264600	IEA					P	HPO:iea[2009-02-17]
OMIM:264600	Pseudovaginal perineoscrotal hypospadias		HP:0000028	OMIM:264600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:108010	Arteriovenous malformation of the brain, somatic		HP:0001442	PMID:29298116	PCS					I	HPO:probinson[2020-07-17]
OMIM:108010	Arteriovenous malformation of the brain, somatic		HP:0002408	PMID:29298116	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-17]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001199	PMID:19061985	PCS		8/20			P	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0000175	PMID:19061985	PCS		HP:0040282			P	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0000193	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0011904	PMID:19061985	PCS		HP:0040282			P	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001629	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001508	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001636	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0000316	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0002779	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0005518	PMID:19061985	PCS					P	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001714	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001643	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001972	PMID:19061985	PCS					P	HPO:probinson[2013-01-09]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001631	PMID:19061985	PCS		3/20			P	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001653	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001510	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0009778	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0000278	OMIM:612561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0000204	PMID:19061985	PCS		HP:0040282			P	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0000347	PMID:19061985	PCS		HP:0040282			P	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0000006	PMID:19061985	PCS					I	HPO:probinson[2013-03-01]
OMIM:612561	Diamond-Blackfan anemia 6		HP:0001634	OMIM:612561	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602772	Retinitis pigmentosa 25		HP:0001133	PMID:18976725	PCS					P	HPO:probinson[2013-02-20]
OMIM:602772	Retinitis pigmentosa 25		HP:0000550	PMID:18976725	PCS					P	HPO:probinson[2013-02-20]
OMIM:602772	Retinitis pigmentosa 25		HP:0007737	PMID:18976725	PCS					P	HPO:probinson[2013-02-20]
OMIM:602772	Retinitis pigmentosa 25		HP:0000662	PMID:18976725	PCS					P	HPO:probinson[2013-02-20]
OMIM:602772	Retinitis pigmentosa 25		HP:0000613	OMIM:602772	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602772	Retinitis pigmentosa 25		HP:0000007	PMID:18976725	PCS					I	HPO:probinson[2013-01-09]
OMIM:602772	Retinitis pigmentosa 25		HP:0000510	PMID:18976725	PCS					P	HPO:probinson[2013-02-20]
OMIM:602772	Retinitis pigmentosa 25		HP:0000543	OMIM:602772	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602772	Retinitis pigmentosa 25		HP:0007787	OMIM:602772	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:602772	Retinitis pigmentosa 25		HP:0007843	PMID:18976725	PCS					P	HPO:probinson[2013-02-20]
OMIM:602772	Retinitis pigmentosa 25		HP:0000533	OMIM:602772	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001254	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0002883	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001250	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001252	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0002240	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0002094	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0034995	OMIM:229700	TAS		1/1			P	HPO:probinson[2024-01-06]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0040301	OMIM:229700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0000737	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0000007	PMID:7763253	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001943	PMID:7763253	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001649	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001946	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001945	OMIM:229700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001942	PMID:7763253	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0002104	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0001259	OMIM:229700	IEA					P	HPO:iea[2009-02-17]
OMIM:229700	Fructose-1,6-bisphosphatase deficiency		HP:0003623	PMID:7763253	PCS		1/1			C	HPO:probinson[2023-02-18]
OMIM:613119	Brugada syndrome 6		HP:0001663	PMID:19122847	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2020-07-22]
OMIM:613119	Brugada syndrome 6		HP:0001695	PMID:19122847	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2020-07-22]
OMIM:613119	Brugada syndrome 6		HP:0012251	PMID:19122847	PCS		4/4			P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-22]
OMIM:613119	Brugada syndrome 6		HP:0000006	PMID:19122847	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-07-22]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0031318	PMID:16651466	PCS		0/1			P	HPO:probinson[2022-07-04]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0001639	PMID:16651466	PCS		1/1			P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0003581	PMID:16651466	PCS					C	HPO:probinson[2022-07-04]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0005110	PMID:16651466	PCS		2/9			P	HPO:probinson[2022-07-04]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0001712	PMID:16651466	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0000006	PMID:16651466	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0001634	PMID:16651466	PCS		1/9			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-07-04]
OMIM:614676	Cardiomyopathy, familial hypertrophic, 21		HP:0001699	PMID:16651466	PCS		2/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-04]
OMIM:602014	Hypomagnesemia 1, intestinal		HP:0001250	PMID:12032570	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-16]
OMIM:602014	Hypomagnesemia 1, intestinal		HP:0002917	PMID:12032570	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-16]
OMIM:602014	Hypomagnesemia 1, intestinal		HP:0003394	OMIM:602014	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602014	Hypomagnesemia 1, intestinal		HP:0003593	PMID:12032570	PCS		5/5			C	HPO:iea[2009-02-17];HPO:probinson[2022-04-16]
OMIM:602014	Hypomagnesemia 1, intestinal		HP:0000007	PMID:12032570	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-16]
OMIM:602014	Hypomagnesemia 1, intestinal		HP:0001281	OMIM:602014	TAS					P	HPO:iea[2009-02-17]
OMIM:602014	Hypomagnesemia 1, intestinal		HP:0002901	OMIM:602014	IEA		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-16]
OMIM:260300	Parkinson disease 15, autosomal recessive		HP:0002322	PMID:25085748	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:260300	Parkinson disease 15, autosomal recessive		HP:0003621	PMID:25085748	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0002067	PMID:18513678;PMID:25085748	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0001300	PMID:18513678	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0001762	PMID:18513678	PCS	HP:0011463	10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0003487	PMID:18513678	PCS	HP:0011462	10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive		HP:0003487	PMID:25085748	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0001332	OMIM:260300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0001260	PMID:25085748;OMIM:260300	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2010-06-18]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0002063	PMID:18513678;PMID:25085748	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:260300	Parkinson disease 15, autosomal recessive		HP:0002141	PMID:25085748	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0002061	OMIM:260300	TAS	HP:0011462	10/10			P	HPO:skoehler[2013-03-31]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0002172	PMID:25085748;OMIM:260300	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:iea[2009-02-17]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0002071	OMIM:260300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0012407	PMID:18513678;PMID:25085748	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2013-11-18];HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0031435	PMID:18513678	PCS		2/9			P	HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0011463	PMID:18513678	PCS		10/10			C	HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0000338	PMID:18513678	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0000514	OMIM:260300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0000007	PMID:18513678	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0002548	PMID:18513678;PMID:25085748	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2010-06-20];HPO:probinson[2022-11-26]
OMIM:260300	Parkinson disease 15, autosomal recessive		HP:0001249	PMID:25085748	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0003677	OMIM:260300	IEA					C	HPO:skoehler[2010-06-19]
OMIM:260300	Parkinson disease 15, autosomal recessive early-onset		HP:0001347	PMID:18513678	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0000563	PMID:36613650	PCS		1/1			P	HPO:probinson[2023-06-10]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0000023	PMID:16252232	PCS		11/14			P	HPO:probinson[2013-03-26]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0009918	PMID:36613650	PCS		1/1			P	HPO:probinson[2023-06-10]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0001131	PMID:16252232;PMID:36613650	PCS		11/11			P	HPO:probinson[2013-03-26];HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0003581	PMID:36613650	PCS		1/1			C	HPO:probinson[2023-06-10]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0007663	PMID:36613650	PCS		1/1			P	HPO:probinson[2023-06-10]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0012038	PMID:16252232	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2023-06-10]
OMIM:609141	Corneal dystrophy, posterior polymorphous, 3		HP:0000006	PMID:16252232	PCS					I	HPO:probinson[2013-03-26];HPO:probinson[2020-07-22]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0002650	PMID:33783914	PCS		2/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0001310	PMID:33783914	PCS	HP:0011462	1/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0001260	PMID:33783914	PCS	HP:0011462	1/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0001252	PMID:33783914	PCS		4/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0001263	PMID:33783914	PCS		4/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0001251	PMID:33783914	PCS		4/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0002080	PMID:33783914	PCS		4/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0000639	PMID:33783914	PCS		1/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0010296	PMID:33783914	PCS		1/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0012450	PMID:33783914	PCS		1/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0011098	PMID:33783914	PCS		1/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0000565	PMID:33783914	PCS		3/4			P	HPO:probinson[2021-07-09]
OMIM:619352	Ataxia, intention tremor, and hypotonia syndrome, childhood-onset		HP:0000006	PMID:33783914	PCS					I	HPO:probinson[2021-07-09];HPO:probinson[2021-07-09]
OMIM:614662	Cortisone reductase deficiency 2		HP:0003621	PMID:21325058	PCS		2/2			C	HPO:probinson[2022-10-11]
OMIM:614662	Cortisone reductase deficiency 2		HP:6000185	PMID:21325058	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:614662	Cortisone reductase deficiency 2		HP:0000855	PMID:21325058	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-11]
OMIM:614662	Cortisone reductase deficiency 2		HP:6001080	PMID:21325058	PCS		2/2			P	HPO:probinson[2024-08-03]
OMIM:614662	Cortisone reductase deficiency 2		HP:0000956	PMID:21325058	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-11]
OMIM:614662	Cortisone reductase deficiency 2		HP:0005616	PMID:21325058	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-11]
OMIM:614662	Cortisone reductase deficiency 2		HP:0012411	PMID:21325058	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-11]
OMIM:614662	Cortisone reductase deficiency 2		HP:0000006	PMID:21325058	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-11]
OMIM:614662	Cortisone reductase deficiency 2		HP:0001513	PMID:21325058	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-11]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002069	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001531	OMIM:614104	TAS					P	HPO:probinson[2013-08-10]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0004322	PMID:23099646	PCS		4/6			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001250	PMID:23099646;PMID:25920557	PCS		14/16			P	HP:probinson[2019-02-24];HP:probinson[2019-02-24];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001251	PMID:26922654;PMID:23099646	PCS		4/8			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0003593	PMID:26922654;PMID:23099646	PCS		2/7			C	HPO:probinson[2022-05-30];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001290	PMID:23099646	PCS		1/1			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0033725	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000319	PMID:26922654;PMID:25920557	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-06-28];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000717	PMID:25920557	PCS		4/10			P	HPO:probinson[2013-08-10];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000752	PMID:23099646;PMID:25167861	PCS		2/3			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001643	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002311	PMID:25920557	PCS		6/9			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000494	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000252	PMID:23099646;PMID:25167861;PMID:25920557	PCS		17/17			P	HPO:probinson[2013-08-10];HP:probinson[2019-02-24];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0003561	PMID:23099646	PCS		5/5			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0011968	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000490	PMID:26922654;PMID:23099646;PMID:25920557	PCS		14/18			P	HPO:probinson[2013-08-10];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-06-28];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001263	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001182	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0011451	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002509	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000767	PMID:26922654;PMID:25167861	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-28];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000601	PMID:23099646	PCS		3/6			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000403	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000648	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000400	PMID:23099646;PMID:25920557	PCS		11/16			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000960	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000006	PMID:25920557	PCS					I	HPO:probinson[2013-01-09];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000369	PMID:26922654	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000126	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000687	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000341	PMID:26922654;OMIM:614104	PCS		12/12			P	HPO:probinson[2013-08-10];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0003577	PMID:26922654;PMID:23099646	PCS		5/7			C	HPO:probinson[2022-05-30];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002120	PMID:23099646	PCS		3/6			P	HPO:probinson[2013-08-10];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002280	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0040082	PMID:23099646	PCS		1/6			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002719	PMID:25920557	PCS		4/9			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0100703	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000414	PMID:26922654;PMID:23099646	PCS		2/3			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0008872	PMID:23099646;PMID:25920557	PCS		13/14			P	HP:probinson[2019-02-24];HPO:probinson[2022-05-30];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001822	OMIM:614104	TAS					P	HPO:probinson[2013-08-10]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000733	PMID:25920557	PCS		8/10			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000219	PMID:25920557	PCS		10/10			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002119	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002714	PMID:26922654	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0012171	PMID:26922654;PMID:23099646	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-28];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000179	PMID:23099646	PCS		3/6			P	HP:probinson[2019-02-24];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000750	PMID:26922654;PMID:23099646;PMID:25920557	PCS		17/17			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-06-28];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001288	PMID:26922654;PMID:23099646	PCS		4/8			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000276	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0002373	PMID:26922654	PCS		1/2			P	HPO:probinson[2013-08-10];HPO:probinson[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000391	PMID:23099646	PCS		1/1			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0005484	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0011344	PMID:23099646;PMID:25167861	PCS		8/8			P	HPO:probinson[2013-08-10];HP:probinson[2019-02-24];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000748	PMID:23099646	PCS		1/6			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001518	PMID:23099646	PCS		5/6			P	HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000426	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0001511	PMID:26922654;PMID:23099646	PCS		2/2			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000347	OMIM:614104;PMID:25920557	PCS		10/11			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-24];HP:probinson[2019-02-24]
OMIM:614104	Intellectual developmental disorder, autosomal dominant 7		HP:0000269	PMID:26922654	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001276	PMID:20729831	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002069	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000340	PMID:20890279	PCS		29/29			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0003577	PMID:20890279	PCS		29/29			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001250	PMID:20729831;PMID:20890279	PCS		2/38			P	HPO:probinson[2022-10-07];HPO:skoehler[2012-11-28];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0003551	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0003593	PMID:20729831	PCS		8/9			C	HPO:probinson[2022-10-07];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002282	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001270	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001508	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0011463	PMID:20729831	PCS		1/9			C	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000718	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000414	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001302	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000752	PMID:20729831	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001269	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001249	PMID:20890279	PCS		29/29			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001348	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001622	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001347	PMID:20729831	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000252	PMID:20729831;PMID:20890279	PCS		38/38			P	HPO:probinson[2022-10-07];HPO:skoehler[2013-06-12];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002353	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000750	PMID:20729831;PMID:20890279	PCS		31/38			P	HPO:probinson[2022-10-07];HPO:skoehler[2013-06-04];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002079	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002970	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002197	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001260	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001285	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001263	PMID:20729831	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0011344	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0010636	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0100710	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001339	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0001558	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000007	PMID:20890279	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002126	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000347	PMID:20729831	PCS		2/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000303	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000028	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0002269	OMIM:604317	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0009879	PMID:20890279	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-07]
OMIM:604317	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations		HP:0000742	PMID:20729831	PCS		1/9			P	HPO:probinson[2022-10-07]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0001792	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0002043	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0002165	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0001395	OMIM:224230	TAS					P	HPO:skoehler[2012-11-26]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000939	OMIM:224230	TAS					P	HPO:skoehler[2012-11-26]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000953	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000579	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0007588	PMID:17507419	PCS		3/3			P	HPO:probinson[2022-11-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0005528	PMID:17507419	PCS		1/3			P	HPO:skoehler[2012-11-26];HPO:probinson[2022-11-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000653	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000972	PMID:17507419	PCS		3/3			P	HPO:probinson[2022-11-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0001249	OMIM:224230	TAS					P	HPO:skoehler[2012-11-26]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0009926	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000670	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000252	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000691	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0001915	PMID:17507419	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0002209	OMIM:224230	IEA					P	HPO:iea[2009-02-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0000007	PMID:17507419	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0008404	PMID:17507419	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0002745	PMID:17507419	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0001059	OMIM:224230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0002206	OMIM:224230	TAS					P	HPO:skoehler[2012-11-26]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0001873	OMIM:224230	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224230	Dyskeratosis congenita, autosomal recessive 1		HP:0001876	PMID:17507419	PCS		1/3			P	HPO:probinson[2022-11-08]
OMIM:619420	Martsolf syndrome 2		HP:0004325	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0000044	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0000252	PMID:30730599;PMID:23420520	PCS		3/3			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0003577	PMID:23420520	PCS		2/2			C	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0006956	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0001264	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0004322	PMID:30730599;PMID:23420520	PCS		3/3			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0031936	PMID:23420520	PCS		2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0002079	PMID:30730599;PMID:23420520	PCS		2/3			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0100490	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0001263	PMID:23420520	PCS		2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0012444	PMID:23420520	PCS		1/2			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0012385	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0000518	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0000519	PMID:23420520	PCS	HP:0003577	2/2			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0001845	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0000007	PMID:23420520	PCS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0000400	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0000455	PMID:30730599	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:619420	Martsolf syndrome 2		HP:0001347	PMID:30730599;PMID:23420520	PCS		2/3			P	HPO:probinson[2021-08-22]
OMIM:158800	Muscular dystrophy, Barnes type		HP:0002486	OMIM:158800	TAS					P	HPO:probinson[2009-02-17]
OMIM:158800	Muscular dystrophy, Barnes type		HP:0003198	OMIM:158800	TAS					P	HPO:skoehler[2010-06-20]
OMIM:158800	Muscular dystrophy, Barnes type		HP:0003560	OMIM:158800	TAS					P	HPO:probinson[2009-02-17]
OMIM:158800	Muscular dystrophy, Barnes type		HP:0000006	OMIM:158800	TAS					I	HPO:probinson[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0006988	PMID:31282990;PMID:31846209	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002025	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0003510	PMID:25142838;PMID:32083401	PCS		11/13			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002023	PMID:31727177	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000365	PMID:25142838;PMID:24739679;PMID:27573763;PMID:29914387;PMID:31727177;PMID:27991736;PMID:20711175	PCS		22/43			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001212	PMID:25142838;PMID:24739679;PMID:29482518;PMID:27922244;PMID:31727177;PMID:24019847;PMID:27991736;PMID:31846209;PMID:32083401	PCS		31/39			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000486	PMID:24739679;PMID:31727177;PMID:25896430	PCS		6/24			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002024	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000089	PMID:35060672;PMID:27991736	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0004322	PMID:24739679;PMID:29914387;PMID:31727177;PMID:27991736	PCS		11/20			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000122	PMID:35060672;PMID:27991736	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002384	PMID:27922244	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0000480	PMID:35060672	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000083	PMID:32083401	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000086	PMID:24739679;PMID:29482518	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0003196	PMID:32083401	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002020	PMID:31949313;PMID:27991736;PMID:32083401	PCS		5/17			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000085	PMID:35060672;PMID:27991736	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0003593	PMID:29482518;PMID:27573763;PMID:31727177;PMID:25896430	PCS		5/17			C	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000081	PMID:27991736	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0033328	PMID:32083401	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0011381	PMID:27991736;PMID:32083401	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0006870	PMID:31846209	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000238	PMID:30509212;PMID:31727177	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0000637	PMID:24739679;PMID:30509212;PMID:29482518;PMID:29914387;PMID:27922244;PMID:31727177;PMID:24019847;PMID:25896430;PMID:31846209	PCS		27/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0008897	PMID:30509212;PMID:29482518;PMID:29914387;PMID:25896430;PMID:32083401	PCS		10/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0040019	PMID:24739679	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0009748	PMID:25142838	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000358	PMID:35060672;PMID:27991736;PMID:32083401	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0003623	PMID:35060672;PMID:29482518;PMID:31727177;PMID:27991736	PCS		6/13			C	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002553	PMID:24739679;PMID:29482518;PMID:29914387;PMID:31727177;PMID:24019847;PMID:25896430;PMID:31846209;PMID:32083401	PCS		22/30			P	HPO:probinson[2009-02-17];HPO:probinson[2024-05-17];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000494	PMID:27573763;PMID:27991736	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000252	PMID:31282990;PMID:31727177;PMID:24019847;PMID:25896430;PMID:31846209	PCS		7/18			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0011800	PMID:31282990	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0010314	OMIM:147920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:147920	Kabuki Syndrome 1		HP:0012584	PMID:32083401	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000407	PMID:35060672;PMID:27991736;PMID:32083401	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0032132	PMID:25142838	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002705	PMID:25142838	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000403	PMID:25142838;PMID:31727177;PMID:24019847	PCS		14/21			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000527	PMID:31727177;PMID:24019847	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0004209	PMID:29482518;PMID:27573763;PMID:31727177;PMID:25896430;PMID:32083401	PCS		6/20			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001973	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki syndrome 1		HP:0000400	PMID:24739679;PMID:35060672;PMID:29482518;PMID:29914387;PMID:31727177;PMID:25896430;PMID:31846209;PMID:32083401	PCS		24/30			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000125	PMID:35060672;PMID:27991736	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000003	PMID:24739679;PMID:35060672;PMID:27991736	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002943	PMID:31949313	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000006	PMID:20711175	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0000369	PMID:30509212;PMID:27991736;PMID:32083401	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0001612	PMID:30509212	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0000126	PMID:35060672;PMID:27922244;PMID:27991736	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0003577	PMID:35060672;PMID:29914387;PMID:27922244;PMID:24019847;PMID:31846209;PMID:32083401	PCS		9/10			C	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0000463	PMID:27991736	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001156	PMID:29482518;PMID:29914387;PMID:24019847	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0004383	PMID:25142838;PMID:24739679;PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		1/30			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001270	PMID:35060672;PMID:31949313;PMID:29482518;PMID:32083401	PCS		4/10			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0100272	PMID:32083401	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0008872	PMID:22126750	PCS		32/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0001943	PMID:31727177	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000579	PMID:35060672	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000219	PMID:29914387;PMID:31727177;PMID:27991736	PCS		7/10			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000218	PMID:30509212;PMID:27573763;PMID:27922244;PMID:27991736;PMID:31846209	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0000851	PMID:31949313	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0006335	PMID:32083401	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000179	PMID:29914387;PMID:27991736	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000457	PMID:31282990;PMID:32083401	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001667	PMID:25142838;PMID:35060672;PMID:31949313;PMID:27573763;PMID:24019847;PMID:27991736	PCS		1/29			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000215	PMID:31727177	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001545	PMID:32083401	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000110	PMID:35060672;PMID:27991736	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0003621	PMID:31727177;PMID:25896430	PCS		4/14			C	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0006956	PMID:30509212	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0001561	PMID:31282990	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000076	PMID:27991736	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000750	PMID:35060672;PMID:31949313;PMID:27573763;PMID:24019847;PMID:27991736;PMID:32083401	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002650	PMID:25142838;PMID:24739679;PMID:25896430;PMID:27991736	PCS		9/35			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000233	PMID:35060672;PMID:32083401	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001684	PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000073	PMID:24739679;PMID:27991736	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000193	PMID:27991736	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000592	PMID:24739679;PMID:25896430	PCS		7/17			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000075	PMID:24739679;PMID:27991736	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001680	PMID:25142838;PMID:24739679;PMID:35060672;PMID:27573763;PMID:31727177;PMID:24019847;PMID:27991736	PCS		4/36			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000074	PMID:27922244	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0002092	PMID:31949313	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0011626	PMID:25142838;PMID:24739679;PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		1/30			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000506	PMID:35060672	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0007099	PMID:24739679	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0011231	OMIM:147920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:147920	Kabuki Syndrome 1		HP:0001718	PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000508	PMID:24739679;PMID:25896430	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0009797	PMID:31727177	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000348	PMID:35060672;PMID:31727177;PMID:27991736;PMID:32083401	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0007655	PMID:24739679;PMID:30509212;PMID:29482518;PMID:27573763;PMID:31727177;PMID:24019847;PMID:31846209	PCS		19/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0008348	PMID:25142838	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000347	PMID:35060672;PMID:30509212;PMID:29482518;PMID:31727177;PMID:25896430	PCS		8/16			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0001650	PMID:25142838;PMID:24739679;PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		1/30			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000286	PMID:31727177	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000164	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki syndrome 1		HP:0001374	PMID:24739679;PMID:31727177;PMID:25896430	PCS		6/23			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0010804	PMID:32083401	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001256	PMID:24739679;PMID:35060672;PMID:31949313;PMID:27922244;PMID:32083401	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0002100	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000161	PMID:31282990	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001250	PMID:24739679;PMID:31727177;PMID:25896430;PMID:31846209	PCS		4/25			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001252	PMID:24739679;PMID:30509212;PMID:29482518;PMID:25896430;PMID:20711175;PMID:31846209	PCS		22/32			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0001373	PMID:22126750	PCS		13/40			P	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0030374	PMID:25142838	PCS		11/13			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0011611	PMID:25142838;PMID:24739679;PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		1/30			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0045075	PMID:30509212;PMID:27573763;PMID:31727177	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0000957	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0011463	PMID:31727177;PMID:25896430	PCS		6/14			C	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000319	PMID:27991736	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0011461	PMID:30509212	PCS		1/1			C	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0001647	PMID:25142838;PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000437	PMID:25142838;PMID:24739679;PMID:30509212;PMID:29482518;PMID:27573763;PMID:27922244;PMID:31727177;PMID:24019847;PMID:25896430;PMID:31846209;PMID:32083401	PCS		38/49			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0000316	PMID:31727177;PMID:32083401	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000954	PMID:29482518;PMID:27573763	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001643	PMID:25142838;PMID:24739679;PMID:35060672;PMID:31949313;PMID:27573763;PMID:31727177;PMID:24019847;PMID:27991736	PCS		5/45			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001488	PMID:27922244	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0000278	PMID:35060672	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001007	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki syndrome 1		HP:0001249	PMID:25142838;PMID:21671394;PMID:29482518;PMID:31727177;PMID:24019847;PMID:25896430	PCS		95/97			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000677	PMID:27991736	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000175	PMID:25142838;PMID:31282990;PMID:30509212;PMID:29914387;PMID:22126750;PMID:20711175;PMID:32083401	PCS		40/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0001385	PMID:30509212;PMID:27573763;PMID:31846209	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0000054	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000453	PMID:35060672;PMID:27991736;PMID:32083401	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002079	PMID:31727177	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0011968	PMID:31949313;PMID:29482518;PMID:31727177;PMID:25896430;PMID:31846209	PCS		8/25			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001382	PMID:24739679;PMID:29482518;PMID:25896430;PMID:27991736	PCS		5/19			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001260	PMID:27922244	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0001263	PMID:25142838;PMID:24739679;PMID:35060672;PMID:29482518;PMID:29914387;PMID:24019847;PMID:20711175;PMID:32083401	PCS		40/42			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000691	PMID:35060672;PMID:32083401	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0010751	PMID:35060672	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0031631	PMID:32083401	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0034198	PMID:31282990	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000689	PMID:32083401	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000601	PMID:31282990;PMID:31846209	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0003316	PMID:24019847	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000960	PMID:24739679;PMID:29482518	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0005218	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001655	PMID:25142838;PMID:35060672;PMID:31949313;PMID:27573763;PMID:31727177;PMID:24019847;PMID:27991736	PCS		5/35			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0005338	PMID:24739679;PMID:29482518;PMID:25896430;PMID:31846209	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000687	PMID:32083401	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000445	PMID:27573763	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0004467	PMID:27991736;PMID:20711175;PMID:32083401	PCS		6/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000023	PMID:31727177	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001750	PMID:35060672;PMID:27573763	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002561	PMID:31949313;PMID:32083401	PCS		5/12			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002162	PMID:29482518;PMID:31727177	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0012806	PMID:31282990	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0011950	PMID:31846209	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002719	PMID:24739679;PMID:31949313;PMID:29482518;PMID:25896430;PMID:22126750	PCS		40/64			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001629	PMID:25142838;PMID:24739679;PMID:35060672;PMID:27573763;PMID:31727177;PMID:24019847;PMID:27991736	PCS		5/36			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0008551	PMID:32083401	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0004736	OMIM:147920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000378	PMID:35060672;PMID:27991736;PMID:32083401	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002557	PMID:31949313;PMID:32083401	PCS		5/12			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000411	PMID:30509212;PMID:27922244;PMID:31846209	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0001741	PMID:35060672	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001744	PMID:35060672;PMID:27573763;PMID:31727177	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000396	PMID:35060672	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001363	PMID:29914387	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0000431	PMID:24739679;PMID:29914387;PMID:31727177	PCS		14/17			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000430	PMID:35060672;PMID:27991736;PMID:32083401	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0005280	PMID:31282990;PMID:32083401	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000829	PMID:32083401	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001878	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001636	PMID:25142838;PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		0/20			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000821	PMID:32083401	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0007334	PMID:27922244	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0000824	PMID:29914387	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0009237	PMID:25142838;PMID:27573763;PMID:27922244	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001511	PMID:31282990	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001631	PMID:25142838;PMID:24739679;PMID:31949313;PMID:31727177;PMID:27991736	PCS		6/15			P	ORCID:0000-0002-0736-9199[2024-05-17];HPO:iea[2009-02-17];HPO:probinson[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0001510	PMID:30509212;PMID:27922244	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki syndrome 1		HP:0000028	PMID:27922244	PCS		1/1	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:147920	Kabuki Syndrome 1		HP:0000028	PMID:31949313	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000028	PMID:29482518	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0000028	PMID:35060672	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0002720	PMID:25142838	PCS		4/13			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki syndrome 1		HP:0002566	OMIM:147920	IEA					P	HPO:iea[2009-02-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001513	PMID:29914387	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:147920	Kabuki Syndrome 1		HP:0001633	PMID:25142838;PMID:35060672;PMID:27573763;PMID:24019847;PMID:27991736	PCS		0/20			P	ORCID:0000-0002-0736-9199[2024-05-17]
OMIM:611097	Intellectual developmental disorder, autosomal recessive 11		HP:0000007	OMIM:611097	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616920	Heart and brain malformation syndrome		HP:0006801	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0000341	PMID:27018474	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0003577	PMID:27018474	PCS		3/3			C	HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0002188	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0000463	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0001250	PMID:27018474	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000260	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0100490	PMID:27018474	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0002283	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0002020	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0011611	PMID:27018474	PCS		1/3			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0410030	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0012444	PMID:27018474	PCS		1/3			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0001629	PMID:27018474	PCS		3/3			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0011220	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000316	PMID:27018474	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0001305	PMID:27018474	PCS		2/3			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000179	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000358	PMID:27018474	PCS		1/3			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0008936	PMID:27018474	PCS		11/13			P	HPO:probinson[2022-08-27];HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0001320	PMID:27018474	PCS		1/3			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0001188	PMID:27018474	PCS		11/12			P	HPO:probinson[2022-08-27];HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0002059	PMID:27018474	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000252	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0001561	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0000431	PMID:27018474	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000232	PMID:27018474	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0002079	PMID:27018474	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0005487	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0009907	PMID:27018474	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0001263	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0005280	PMID:27018474	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0002509	PMID:27018474	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000007	PMID:27018474	PCS					I	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0002705	PMID:27018474	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000568	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:616920	Heart and brain malformation syndrome		HP:0000505	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0001510	PMID:27018474	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000369	PMID:27018474	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616920	Heart and brain malformation syndrome		HP:0000269	PMID:27018474	PCS					P	HPO:probinson[2017-06-23]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0002069	PMID:15827091	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0003621	PMID:15827091	PCS		3/10			C	HPO:probinson[2022-09-02]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0002373	PMID:15827091	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0002121	PMID:15827091	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0011463	PMID:15827091	PCS		5/10			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0010818	PMID:15827091	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0003593	PMID:15827091	PCS		2/10			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:609800	Generalized epilepsy with febrile seizures plus, type 4		HP:0000006	PMID:15827091	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000220	PMID:23621916	PCS		1/4			P	HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000582	PMID:23621916	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0008209	PMID:23621916	PCS		1/4			P	HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0003577	PMID:23621916	PCS		2/4			C	HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000122	PMID:23621916	PCS		1/4			P	HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000085	PMID:23621916	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0003593	PMID:23621916	PCS		2/4			C	HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0012745	PMID:23621916	PCS		4/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0001629	PMID:23621916	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0009765	PMID:23621916	PCS		4/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0001643	PMID:23621916	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0001249	PMID:23621916	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000670	PMID:23621916	PCS		4/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0030127	PMID:23621916	PCS		1/4			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000252	PMID:23621916	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000010	PMID:23621916	PCS		2/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0003189	PMID:23621916	PCS		4/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000490	PMID:23621916	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0001263	PMID:23621916	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0009890	PMID:23621916	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000007	PMID:23621916	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000689	PMID:23621916	PCS		2/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000348	PMID:23621916	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000545	PMID:23621916	PCS		2/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-09-08]
OMIM:613680	Beaulieu-Boycott-Innes syndrome		HP:0000347	PMID:23621916	PCS		1/4			P	HPO:probinson[2022-09-08]
OMIM:115900	Cataract 42		HP:0003577	PMID:23508780	PCS		9/10			C	HPO:probinson[2023-02-17]
OMIM:115900	Cataract 42		HP:0000518	PMID:23508780	PCS		10/10			P	HPO:probinson[2023-02-17]
OMIM:115900	Cataract 42		HP:0011462	PMID:23508780	PCS		1/10			C	HPO:probinson[2023-02-17]
OMIM:115900	Cataract 42		HP:0000519	PMID:23508780	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-17]
OMIM:115900	Cataract 42		HP:0000006	PMID:23508780	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:115900	Cataract 42		HP:0000501	PMID:23508780	PCS		HP:0040283			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-17]
OMIM:115900	Cataract 42		HP:0000545	PMID:23508780	PCS		HP:0040283			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-17]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0030953	PMID:11115159	PCS		11/25			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002102	PMID:11115159	PCS		10/25			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0001055	PMID:23965844	PCS		7/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0003552	OMIM:142680	IEA					P	HPO:iea[2009-02-17]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0025289	PMID:23965844	PCS		41/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002240	PMID:23965844	PCS		9/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0040313	PMID:23965844	PCS		15/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0012450	PMID:23965844	PCS		21/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002315	PMID:11115159	PCS		17/25			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002239	PMID:23965844	PCS		3/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0003326	PMID:23965844;PMID:11115159	PCS		131/183			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0003565	OMIM:142680	IEA					P	HPO:iea[2009-02-17]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002653	PMID:23965844	PCS		6/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0005764	PMID:23965844	PCS		2/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002013	PMID:23965844	PCS		28/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:4000041	PMID:23965844	PCS	HP:0003581	16/158			P	HPO:probinson[2021-06-13]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002829	PMID:23965844;PMID:11115159	PCS		114/183			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0100539	PMID:23965844;PMID:11115159	PCS		43/183			P	HPO:probinson[2020-10-26];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0040186	PMID:23965844	PCS		41/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0000509	PMID:23965844	PCS		35/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0100614	PMID:23965844	PCS		3/158			P	HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0001954	PMID:23965844;PMID:11115159	PCS		157/183			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0012280	OMIM:142680	TAS					P	HPO:probinson[2013-04-07]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0000988	PMID:11115159	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0000006	PMID:10199409	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002027	PMID:23965844;PMID:11115159	PCS		132/183			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-26];HPO:probinson[2020-10-26]
OMIM:142680	Periodic fever, familial, autosomal dominant		HP:0002028	PMID:23965844	PCS		28/158			P	HPO:probinson[2020-10-26]
OMIM:258660	Nonarteritic anterior ischemic optic neuropathy, susceptibility to		HP:0000007	OMIM:258660	IEA					I	HPO:iea[2009-02-17]
OMIM:258660	Nonarteritic anterior ischemic optic neuropathy, susceptibility to		HP:0007634	OMIM:258660	IEA					P	HPO:iea[2009-02-17]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0000252	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0000054	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0000046	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001272	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0011968	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0002098	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001250	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001263	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001252	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0012345	PMID:23842455	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0003819	PMID:23842455	PCS		1/1			C	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001508	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0011461	PMID:23842455	PCS		1/1			C	HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0000007	PMID:23842455	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0000648	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001511	PMID:23842455	PCS	HP:0011461	1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001873	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0000028	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615597	Congenital disorder of glycosylation, type Ix		HP:0001249	PMID:23842455	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:614851	Seckel syndrome 7		HP:0003510	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0001385	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0000252	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0003577	PMID:22933543	PCS		2/2			C	HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0000013	PMID:22933543	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0002750	PMID:22933543	PCS	HP:0011463	2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0001250	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0003067	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0004220	PMID:22933543	PCS		1/2			P	HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0001191	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0011344	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0011787	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0008551	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0000448	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0000007	PMID:22933543	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0000601	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0004209	PMID:22933543	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0001511	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0004626	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-06];HPO:probinson[2023-02-12]
OMIM:614851	Seckel syndrome 7		HP:0000786	PMID:22933543	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000473	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000054	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0003764	OMIM:611929	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0006109	OMIM:611929	TAS					P	HPO:skoehler[2013-04-18]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0001245	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0002750	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0003298	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0001252	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0001263	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000272	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000470	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0001290	OMIM:611929	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0010487	OMIM:611929	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0012368	OMIM:611929	TAS					P	HPO:skoehler[2013-10-22]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0012385	OMIM:611929	TAS					P	HPO:skoehler[2013-10-22]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000506	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0009473	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000316	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0430007	OMIM:611929	TAS					P	HPO:skoehler[2015-12-30]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000278	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000377	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000465	OMIM:611929	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611929	Camptodactyly syndrome, Guadalajara, type III		HP:0000006	OMIM:611929	IEA					I	HPO:skoehler[2010-06-19]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0001396	PMID:27319779	PCS	HP:0003623	4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0003676	PMID:27319779	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0000076	PMID:27319779	PCS		1/4			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0000365	PMID:27319779	PCS		0/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0001399	PMID:27319779	PCS		4/4			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0001541	PMID:27469900	PCS		1/7			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0030991	PMID:27469900	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0030991	PMID:27319779	PCS	HP:0003623	4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0001394	PMID:27319779	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0002240	PMID:27469900	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0003593	PMID:27469900	PCS		5/7			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0030948	PMID:27469900	PCS		7/7			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0012852	PMID:27469900	PCS		4/7			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0011985	PMID:27319779;PMID:27469900	PCS		6/11			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0034294	PMID:27469900	PCS		4/7			P	HPO:probinson[2022-09-05]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0001409	PMID:27319779	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0006580	PMID:27319779	PCS		4/4			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0001408	PMID:27319779;PMID:27469900	PCS		6/11			P	HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0000007	PMID:27319779	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0000989	PMID:27469900	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0002613	PMID:27469900	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0000952	PMID:27469900	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0001744	PMID:27469900	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:617394	Sclerosing cholangitis, neonatal		HP:0003623	PMID:27319779;PMID:27469900	PCS		6/11			C	HPO:probinson[2022-06-14]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0003477	PMID:36331550;PMID:35150594	PCS		4/27			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0003577	PMID:35150594	PCS		4/22			C	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001332	PMID:36331550;PMID:35150594	PCS		2/28			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001250	PMID:36331550;PMID:35150594	PCS		4/28			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];HPO:probinson[2024-03-29];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001272	PMID:36331550	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0002064	PMID:36331550	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001251	PMID:36331550;PMID:35150594	PCS		14/28			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0000639	PMID:36331550	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0007340	PMID:36331550;PMID:35150594	PCS		16/21			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0011463	PMID:35150594	PCS		4/22			C	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0011462	PMID:35150594	PCS		2/22			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0007166	PMID:35150594	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001249	PMID:36331550;PMID:35150594	PCS		5/28			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0003202	PMID:36331550	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0000252	PMID:36331550;PMID:35150594	PCS		0/28			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0003621	PMID:36331550;PMID:35150594	PCS		15/25			C	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0002650	PMID:35150594	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001761	PMID:36331550;PMID:35150594	PCS		6/28			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2024-03-12];HPO:probinson[2024-03-29]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001288	PMID:35150594	PCS		15/15			P	HPO:probinson[2024-03-12]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0003487	PMID:36331550	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0003484	PMID:36331550	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001382	PMID:35150594	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0002495	PMID:36331550	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001260	PMID:35150594	PCS		1/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0009053	PMID:35150594	PCS		9/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0007256	PMID:35150594	PCS		19/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001258	PMID:36331550;PMID:35150594	PCS		21/28			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0000006	PMID:35150594	PCS					I	HPO:probinson[2024-03-12]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001138	PMID:35150594	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620538	Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia		HP:0001336	PMID:35150594	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:615583	Verheij syndrome		HP:0000341	PMID:27804958	PCS		3/5			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0003577	PMID:27804958	PCS		6/6			C	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000343	PMID:27804958	PCS		6/6			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000321	PMID:27804958	PCS		5/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000089	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615583	Verheij syndrome		HP:0004322	OMIM:615583;PMID:27804958	PCS		15/16			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000463	PMID:27804958	PCS		5/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0001250	PMID:24140112	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0003196	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615583	Verheij syndrome		HP:0001629	PMID:27804958	PCS		3/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0002937	PMID:24140112	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0011220	PMID:27804958	PCS		6/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000219	PMID:27804958	PCS		5/6			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0030084	OMIM:615583	TAS					P	HPO:skoehler[2014-09-21]
OMIM:615583	Verheij syndrome		HP:0000455	PMID:27804958	PCS		6/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000278	PMID:24140112	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0002059	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615583	Verheij syndrome		HP:0000252	PMID:24140112	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000175	PMID:24140112	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0001660	PMID:27804958	PCS		1/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0002650	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615583	Verheij syndrome		HP:0000431	PMID:27804958	PCS		4/6			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0011968	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615583	Verheij syndrome		HP:0000293	PMID:27804958	PCS		4/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0001382	PMID:27804958	PCS		5/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0001263	PMID:24140112;PMID:27804958	PCS		7/7			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000470	PMID:27804958	PCS		4/6			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000609	PMID:27804958	PCS		2/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0001518	PMID:24140112	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0002827	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615583	Verheij syndrome		HP:0002948	PMID:27804958	PCS		1/6			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000107	OMIM:615583	TAS					P	HPO:skoehler[2014-04-04]
OMIM:615583	Verheij syndrome		HP:0009796	PMID:27804958	PCS		2/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0009237	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615583	Verheij syndrome		HP:0001511	PMID:27804958	PCS		3/6			P	HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0001510	PMID:24140112	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000006	PMID:24140112	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000589	PMID:27804958	PCS		1/6			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-06-09]
OMIM:615583	Verheij syndrome		HP:0000104	OMIM:615583	TAS					P	HPO:skoehler[2014-02-06]
OMIM:614845	Nephronophthisis 15		HP:0001320	PMID:22863007	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0000639	PMID:22863007	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0001250	PMID:22863007	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0001263	PMID:22863007	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0000618	PMID:22863007	PCS		2/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0000007	PMID:22863007	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0000090	PMID:22863007	PCS		6/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0000546	PMID:22863007	PCS		6/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0010442	PMID:22863007	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0002910	PMID:22863007	PCS		1/7			P	HPO:probinson[2023-02-11]
OMIM:614845	Nephronophthisis 15		HP:0001513	PMID:22863007	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-11]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0003596	PMID:17186461	PCS		2/3			C	HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0011705	PMID:17186461	PCS		1/3			P	HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0001635	PMID:17186461	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0001712	PMID:17186461	PCS		2/3			P	HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0011713	PMID:17186461	PCS		1/3			P	HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0025710	PMID:17186461	PCS		1/3			C	HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0001279	PMID:17186461	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0033755	PMID:17186461	PCS		3/3			P	HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0000006	PMID:17186461	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0012666	PMID:17186461	PCS		3/3			P	HPO:probinson[2022-07-03]
OMIM:613694	Cardiomyopathy, dilated, 1U		HP:0001644	PMID:17186461	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002421	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000486	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0004322	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001250	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001252	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0003593	PMID:38622837	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0033128	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0031545	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0033207	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001727	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000316	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001888	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0410028	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0004315	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0003623	PMID:31775018	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0003565	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000175	PMID:35637269;PMID:38622837	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000252	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000331	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001263	PMID:35637269;PMID:31775018;PMID:38622837	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0030386	PMID:31775018	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0003160	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0032128	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0009098	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0033222	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000007	PMID:31775018	PCS					I	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000047	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0008843	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002028	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0003577	PMID:35637269	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0003212	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000023	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001392	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0011839	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002240	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0031402	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0040197	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001903	PMID:31775018;PMID:38622837	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001944	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0006532	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001269	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002633	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0030842	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0000750	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:6001197	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0031936	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0410242	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0410243	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002572	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0410240	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0410241	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002171	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0005086	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0010975	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0011227	PMID:31775018;PMID:38622837	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0012683	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0040089	PMID:35637269	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001954	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002329	PMID:38622837	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0001873	PMID:31775018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621140	Congenital disorder of glycosylation type 1EE with or without immunodeficiency		HP:0002721	PMID:35637269	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:609814	Complement factor H deficiency		HP:0003621	OMIM:609814	IEA					C	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0005369	OMIM:609814	IEA					P	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0005389	OMIM:609814	IEA					P	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0000790	OMIM:609814	IEA					P	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0002718	OMIM:609814	IEA					P	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0000007	OMIM:609814	IEA					I	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0004746	OMIM:609814	IEA					P	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0000006	OMIM:609814	IEA					I	HPO:iea[2009-02-17]
OMIM:609814	Complement factor H deficiency		HP:0012622	OMIM:609814	TAS					P	HPO:probinson[2014-01-18]
OMIM:609814	Complement factor H deficiency		HP:0004722	OMIM:609814	IEA					P	HPO:iea[2009-02-17]
OMIM:219600	Cystic disease of lung		HP:0002719	OMIM:219600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:219600	Cystic disease of lung		HP:0000007	OMIM:219600	TAS					I	HPO:skoehler[2009-02-17]
OMIM:219600	Cystic disease of lung		HP:0005948	OMIM:219600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:219600	Cystic disease of lung		HP:0004876	OMIM:219600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:254700	Myeloproliferative disease, autosomal recessive		HP:0004852	OMIM:254700	IEA					P	HPO:iea[2009-02-17]
OMIM:254700	Myeloproliferative disease, autosomal recessive		HP:0000007	OMIM:254700	IEA					I	HPO:iea[2009-02-17]
OMIM:254700	Myeloproliferative disease, autosomal recessive		HP:0005547	OMIM:254700	IEA					P	HPO:iea[2009-02-17]
OMIM:620276	Oocyte/zygote/embryo maturation arrest 14		HP:0034914	PMID:32666501	PCS		5/5			P	HPO:probinson[2023-07-18]
OMIM:620276	Oocyte/zygote/embryo maturation arrest 14		HP:0008222	PMID:32666501	PCS		5/5			P	HPO:probinson[2023-07-07]
OMIM:620276	Oocyte/zygote/embryo maturation arrest 14		HP:0011462	PMID:32666501	PCS		5/5			C	HPO:probinson[2023-07-07]
OMIM:620276	Oocyte/zygote/embryo maturation arrest 14		HP:0000007	PMID:32666501	PCS					I	HPO:probinson[2023-07-07]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002069	PMID:26467484	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0000341	PMID:30985297	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002345	PMID:26467484	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002067	PMID:26467484	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002188	PMID:30985297	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0010527	PMID:26467484	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002186	PMID:26467484	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001272	PMID:26467484	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0031629	PMID:26467484	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001250	PMID:30985297	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002063	PMID:26467484	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0003593	PMID:26467484	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001350	PMID:26467484	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0011812	PMID:26467484	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001270	PMID:15746149	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0033725	PMID:30985297	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0000338	PMID:26467484	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001249	PMID:26467484	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0003623	PMID:30985297	PCS		1/1			C	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001265	PMID:26467484	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002059	PMID:26467484;PMID:30985297	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0000750	PMID:15746149	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001300	PMID:26467484	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0003487	PMID:26467484	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001288	PMID:26467484	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002079	PMID:26467484	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001263	PMID:26467484	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001419	PMID:26467484	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002307	PMID:26467484	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0002527	PMID:26467484	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300423	Intellectual developmental disorder, X-linked syndromic, Hedera type		HP:0001257	PMID:30985297	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0001298	PMID:37656279	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000343	PMID:37656279	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0010946	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0001134	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0001250	PMID:37656279	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0030674	PMID:37656279	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0025664	PMID:37656279	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0002181	PMID:37656279	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0010783	PMID:37656279	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000958	PMID:37656279	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0008551	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0012472	PMID:37656279	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0500049	PMID:37656279	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000316	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000656	PMID:37656279	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0008897	PMID:37656279	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000278	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0001347	PMID:37656279	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000494	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0011968	PMID:37656279	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0005281	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0012382	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0001712	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000007	PMID:37656279	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0007479	PMID:37656279	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0001511	PMID:37656279	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0000586	PMID:37656279	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0001631	PMID:37656279	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620510	Xerosis and growth failure with immune and pulmonary dysfunction syndrome		HP:0004349	PMID:37656279	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0001133	PMID:17325280	PCS		1/1			P	HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0003621	PMID:17325280	PCS		1/1			C	HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0000662	PMID:17325280	PCS		1/1			P	HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0001761	OMIM:614879	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0001271	PMID:17325280	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0001251	OMIM:614879	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0002460	PMID:17325280	PCS		1/1			P	HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0010632	PMID:17325280	PCS		1/1			P	HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0008064	OMIM:614879	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0000518	OMIM:614879	TAS	HP:0003577				P	HPO:probinson[2013-02-24]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0000407	PMID:17325280	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0010571	PMID:17325280	PCS		1/1			P	HPO:probinson[2013-02-24]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0000458	OMIM:614879	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0000007	PMID:17325280	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0007663	PMID:17325280	PCS		1/1			P	HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0001638	PMID:17325280	PCS	HP:0003581	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0001324	OMIM:614879	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0000510	PMID:17325280	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2023-05-20]
OMIM:614879	Peroxisome biogenesis disorder 9B		HP:0001249	OMIM:614879	TAS					P	HPO:probinson[2013-02-24]
OMIM:163100	Nevus flammeus of nape of neck		HP:0007616	OMIM:163100	IEA					P	HPO:iea[2009-02-17]
OMIM:163100	Nevus flammeus of nape of neck		HP:0000006	OMIM:163100	IEA					I	HPO:iea[2009-02-17]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0002069	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0003577	PMID:36067010	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000023	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000260	PMID:36067010	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0003593	PMID:36067010	PCS		3/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0004383	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0033725	PMID:36067010	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0012469	PMID:36067010	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0012110	PMID:36067010	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0032660	PMID:36067010	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000954	PMID:36067010	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000316	PMID:36067010	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0100806	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000256	PMID:36067010	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0004415	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0003623	PMID:36067010	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000574	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0011968	PMID:36067010	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0200128	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0011800	PMID:36067010	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0011344	PMID:36067010	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0011703	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0034197	PMID:36067010	PCS		2/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0034198	PMID:36067010	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0031165	PMID:36067010	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0006682	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000822	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0001537	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000646	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000007	PMID:36067010	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000505	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000527	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0002007	PMID:36067010	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0002205	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0007359	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0002126	PMID:36067010	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000369	PMID:36067010	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000787	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000028	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620504	Developmental and epileptic encephalopathy 111		HP:0000666	PMID:36067010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0031417	OMIM:167400	IEA					P	HPO:skoehler[2019-04-18]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0001662	OMIM:167400	IEA					P	HPO:skoehler[2009-02-17]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0031284	PMID:17145499	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0200026	PMID:17145499	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-13]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0500005	PMID:17145499	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0200025	PMID:17145499	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-13]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0001649	OMIM:167400	IEA					P	HPO:skoehler[2009-02-17]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0000006	PMID:17145499	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-13]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0000632	OMIM:167400	IEA					P	HPO:skoehler[2009-02-17]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0007328	OMIM:167400	IEA					P	HPO:skoehler[2009-02-17]
OMIM:167400	Paroxysmal extreme pain disorder		HP:0003623	PMID:17145499	PCS					C	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-13]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0003577	PMID:9915973	PCS		1/1			C	HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000054	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0001795	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0002133	PMID:9915973	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0001371	PMID:9915973	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0003196	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0002251	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0001182	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0012332	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0001629	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000822	PMID:9915973	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000426	PMID:9915973	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000414	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0001649	PMID:9915973	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000713	PMID:9915973	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000378	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0001643	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0001631	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000006	PMID:9915973	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0000358	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613870	Hirschsprung disease, cardiac defects, and autonomic dysfunction		HP:0009626	PMID:9915973	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001397	PMID:19726876	PCS		1/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003236	PMID:19726876	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003552	OMIM:613327;PMID:19726876	PCS		11/14			P	HPO:probinson[2022-09-29];HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001371	PMID:19726876	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002021	OMIM:613327	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0005110	PMID:19726876	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002240	PMID:19726876	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003593	OMIM:613327	IEA					C	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0000939	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001508	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002719	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0000938	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0033794	PMID:19726876	PCS		2/5			P	HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0000855	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0009125	PMID:19726876	PCS		5/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002617	OMIM:613327	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0000956	PMID:19726876	PCS		0/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003307	PMID:19726876	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001649	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0006532	PMID:19726876	PCS		2/5			P	HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001544	PMID:19726876	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003701	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001324	PMID:19726876	PCS		3/5			P	HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002019	PMID:19726876	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002910	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003306	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001007	OMIM:613327	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001744	PMID:19726876	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003546	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003326	PMID:19726876	PCS		1/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002015	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003324	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003687	PMID:19726876	PCS		5/5			P	HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002155	PMID:19726876	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002595	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002650	PMID:19726876	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001662	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0011968	OMIM:613327	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003560	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003719	PMID:19726876	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0000007	PMID:19726876	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0001657	OMIM:613327	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003712	PMID:19726876	PCS		3/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0005616	PMID:19726876	PCS		1/5			P	HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0002720	OMIM:613327	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0000842	PMID:19726876	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-29]
OMIM:613327	Lipodystrophy, congenital generalized, type 4		HP:0003557	PMID:19726876	PCS		5/5			P	HPO:probinson[2022-09-29]
OMIM:617141	Aniridia 2		HP:0003577	PMID:21321669	PCS		5/5			C	HPO:probinson[2022-08-03]
OMIM:617141	Aniridia 2		HP:0001132	PMID:21321669	PCS		1/5			P	HPO:probinson[2022-08-03]
OMIM:617141	Aniridia 2		HP:0000518	PMID:21321669	PCS		2/5			P	HPO:probinson[2019-04-20];HPO:probinson[2022-08-03]
OMIM:617141	Aniridia 2		HP:0000646	PMID:21321669	PCS		2/5			P	HPO:probinson[2022-08-03]
OMIM:617141	Aniridia 2		HP:0000612	PMID:21321669	PCS		3/5			P	HPO:probinson[2022-08-03]
OMIM:617141	Aniridia 2		HP:0000648	PMID:21321669	PCS		2/5			P	HPO:probinson[2022-08-03]
OMIM:617141	Aniridia 2		HP:0000526	PMID:21321669	PCS		2/5		HP:0012832	P	HPO:probinson[2019-04-20];HPO:probinson[2022-08-03]
OMIM:617141	Aniridia 2		HP:0000006	PMID:21321669	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-03]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0003577	PMID:24676357	PCS		2/2			C	HPO:probinson[2023-03-29];HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0004467	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0001520	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000463	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000023	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0001442	PMID:24676357	PCS		2/2			I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000260	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0001263	PMID:24676357	PCS		1/2			P	HPO:skoehler[2019-04-18]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0032445	PMID:24676357	PCS		2/2			P	HPO:probinson[2023-03-29];HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0005280	PMID:24676357	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0002808	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000717	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000316	PMID:24676357	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0001548	PMID:24676357	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000767	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0001537	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0001538	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0002007	PMID:24676357	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0002667	PMID:24676357	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000256	PMID:24676357	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000960	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000105	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:618272	Global developmental delay, lung cysts, overgrowth, and wilms tumor		HP:0000347	PMID:24676357	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0002465	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001276	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0003698	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0002188	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0002024	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0000160	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001252	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0003076	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001394	PMID:26189817	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0012444	PMID:26189817	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001508	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0000737	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0011462	PMID:26189817	PCS		1/2			C	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001324	PMID:26189817	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0040217	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0003688	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0002017	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0003128	PMID:26189817	PCS		2/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001347	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0002875	PMID:26189817	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0003546	PMID:26189817	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0003623	PMID:26189817	PCS		1/2			C	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001265	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0003487	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0011968	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0011924	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0002151	PMID:26189817	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001263	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0000592	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0002094	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0004691	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0011923	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001639	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001738	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0009830	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0000007	PMID:26189817	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0008347	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001257	PMID:26189817	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0000124	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0000325	PMID:26189817	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001337	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616539	Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay		HP:0001952	PMID:26189817	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:192310	Vasculitis, lymphocytic, nodular		HP:0005300	OMIM:192310	IEA					P	HPO:iea[2009-02-17]
OMIM:192310	Vasculitis, lymphocytic, nodular		HP:0001939	OMIM:192310	IEA					P	HPO:iea[2009-02-17]
OMIM:192310	Vasculitis, lymphocytic, nodular		HP:0000006	OMIM:192310	IEA					I	HPO:iea[2009-02-17]
OMIM:109130	Axial osteomalacia		HP:0003236	OMIM:109130	TAS					P	HPO:probinson[2009-02-17]
OMIM:109130	Axial osteomalacia		HP:0003198	OMIM:109130	TAS					P	HPO:probinson[2009-02-17]
OMIM:109130	Axial osteomalacia		HP:0011001	OMIM:109130	TAS					P	HPO:probinson[2009-02-17]
OMIM:109130	Axial osteomalacia		HP:0000107	OMIM:109130	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109130	Axial osteomalacia		HP:0002749	OMIM:109130	TAS					P	HPO:probinson[2009-02-17]
OMIM:109130	Axial osteomalacia		HP:0003701	OMIM:109130	TAS					P	HPO:probinson[2009-02-17]
OMIM:109130	Axial osteomalacia		HP:0000006	OMIM:109130	TAS					I	HPO:probinson[2009-02-17]
OMIM:109130	Axial osteomalacia		HP:0006557	OMIM:109130	IEA					P	HPO:skoehler[2012-10-12]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0002135	PMID:23176821	PCS		3/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0003477	PMID:23176821	PCS		5/7			P	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0003577	PMID:23176821	PCS		1/7			C	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0003621	PMID:23176821	PCS		1/7			C	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0003487	PMID:23176821	PCS		7/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0031936	PMID:23176821	PCS		4/7			P	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0002079	PMID:23176821	PCS		3/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0001332	PMID:23176821	PCS		1/7			P	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0002395	PMID:23176821	PCS		7/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0003593	PMID:23176821	PCS		1/7			C	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0001270	PMID:23176821	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0100543	PMID:23176821	PCS		1/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0007350	PMID:23176821	PCS		4/7			P	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0011463	PMID:23176821	PCS		4/7			C	HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0000007	PMID:23176821	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0002317	PMID:23176821	PCS		2/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0030051	PMID:23176821	PCS		2/7			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0001258	PMID:23176821	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0002500	PMID:23176821	PCS		3/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-03]
OMIM:615030	Spastic paraplegia 56, autosomal recessive		HP:0001249	PMID:23176821	PCS		1/7			P	HPO:probinson[2022-03-03]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000286	PMID:24716670	PCS		3/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000684	OMIM:180700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0005852	PMID:24716670	PCS		2/6			P	HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000200	PMID:24716670	PCS		3/6			P	HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0004322	PMID:24716670	PCS	HP:0003593	6/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001052	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0003196	PMID:24716670	PCS		6/6			P	HPO:probinson[2013-04-09];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0010297	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000316	PMID:24716670	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000678	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0009466	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000637	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000158	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0010290	OMIM:180700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000278	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001249	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000358	PMID:24716670	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000494	PMID:24716670	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000054	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0002750	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001263	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0011800	OMIM:180700	TAS					P	HPO:skoehler[2013-11-28]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0003083	PMID:24716670	PCS		2/6			P	HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000767	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001537	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000527	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000207	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000202	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000520	PMID:24716670	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000960	PMID:24716670	PCS		3/6			P	HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000006	PMID:19918918	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000369	PMID:24716670	PCS		2/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001853	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000126	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0003577	PMID:24716670	PCS		6/6			C	HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000582	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000343	PMID:24716670	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000189	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0008905	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000463	PMID:24716670	PCS		3/6			P	HPO:probinson[2013-04-09];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001156	PMID:24716670	PCS		6/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000023	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0002164	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000260	PMID:24716670	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0004220	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000060	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0012368	PMID:24716670	PCS		3/6			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001705	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0009883	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000219	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0030084	OMIM:180700	TAS					P	HPO:skoehler[2014-09-21]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0002714	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000218	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000059	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0006335	PMID:24716670	PCS		2/6			P	HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000212	PMID:24716670	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000256	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0003026	PMID:24716670	PCS		5/6			P	HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0003027	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0004279	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000431	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000075	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000272	PMID:24716670	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000470	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0005280	PMID:24716670	PCS		3/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0011304	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0001837	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0002007	OMIM:180700	IEA					P	HPO:iea[2009-02-17]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0200055	OMIM:180700	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000028	PMID:24716670	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:180700	Robinow syndrome, autosomal dominant 1		HP:0000347	PMID:24716670	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:604129	Epidermolysis bullosa pruriginosa		HP:0001056	OMIM:604129	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604129	Epidermolysis bullosa pruriginosa		HP:0001030	OMIM:604129	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604129	Epidermolysis bullosa pruriginosa		HP:0002164	OMIM:604129	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604129	Epidermolysis bullosa pruriginosa		HP:0000007	OMIM:604129	IEA					I	HPO:skoehler[2010-06-19]
OMIM:604129	Epidermolysis bullosa pruriginosa		HP:0008404	OMIM:604129	TAS					P	HPO:skoehler[2013-05-03]
OMIM:604129	Epidermolysis bullosa pruriginosa		HP:0000006	PMID:9182828	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-07]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0003577	PMID:22246504	PCS		6/6			C	HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0025114	PMID:22246504	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0000007	PMID:22246504	PCS					I	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0001019	PMID:22246504	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0025080	PMID:22246504	PCS					P	HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0007479	PMID:22246504	PCS	HP:0003577	6/6			P	HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0000982	PMID:22246504	PCS		6/6			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0007503	PMID:22246504	PCS		6/6			P	HPO:probinson[2022-03-16]
OMIM:615024	Ichthyosis, congenital, autosomal recessive 10		HP:0000962	PMID:22246504	PCS					P	HPO:probinson[2022-03-16]
OMIM:268210	Rhabdomyosarcoma 1		HP:0000007	OMIM:268210	IEA					I	HPO:iea[2009-02-17]
OMIM:268210	Rhabdomyosarcoma 1		HP:0006743	OMIM:268210	IEA					P	HPO:iea[2009-02-17]
OMIM:104400	Amelia and terminal transverse hemimelia		HP:0009827	OMIM:104400	IEA					P	HPO:iea[2009-02-17]
OMIM:104400	Amelia and terminal transverse hemimelia		HP:0001426	OMIM:104400	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:104400	Amelia and terminal transverse hemimelia		HP:0000006	OMIM:104400	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:149500	Kyrle disease		HP:0007787	OMIM:149500	IEA					P	HPO:iea[2009-02-17]
OMIM:149500	Kyrle disease		HP:0000006	OMIM:149500	IEA					I	HPO:iea[2009-02-17]
OMIM:149500	Kyrle disease		HP:0000951	OMIM:149500	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0001382	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0001065	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0000987	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0000007	OMIM:225310	IEA					I	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0000967	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0000978	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0000963	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0000974	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:225310	Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality		HP:0001634	OMIM:225310	IEA					P	HPO:iea[2009-02-17]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0002015	PMID:28002403	PCS	HP:0003596	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0003676	PMID:28002403	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0006858	PMID:28002403	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0001310	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0001272	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0001260	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0002066	PMID:28002403	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0001284	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0002460	PMID:28002403	PCS	HP:0003596	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0002075	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0001152	PMID:28002403	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0002070	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0007141	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0000657	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0000007	PMID:28002403	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0002317	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0025710	PMID:28002403	PCS		1/1			C	HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0002403	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0006886	PMID:28002403	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0007338	PMID:28002403	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617633	Spinocerebellar ataxia, autosomal recessive 26		HP:0000666	PMID:28002403	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001331	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000286	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0003577	OMIM:618500	IEA		2/3			C	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000340	OMIM:618500	IEA		1/3			P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001234	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000343	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0002384	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001250	PMID:31006513	PCS		0/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001274	PMID:31006513	PCS		2/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001290	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0010669	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0100651	OMIM:618500	IEA		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0031964	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0008551	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0100801	PMID:31006513	PCS		3/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0006870	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000218	OMIM:618500	IEA		1/3			P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000873	OMIM:618500	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001324	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0003623	PMID:31006513	PCS		1/3			C	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000252	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0002079	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001263	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0011467	PMID:31006513	PCS		2/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0030948	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0005280	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001738	PMID:31006513	PCS		2/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000407	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001518	PMID:31006513	PCS		2/3			P	HPO:probinson[2023-03-16];HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000601	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0002507	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000405	OMIM:618500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001511	OMIM:618500	IEA		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0003811	PMID:31006513	PCS		1/3			C	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001510	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0001257	OMIM:618500	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000006	PMID:31006513	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-16]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000369	OMIM:618500	IEA		2/3			P	HPO:skoehler[2019-09-07]
OMIM:618500	Holoprosencephaly 12 with or without pancreatic agenesis		HP:0000269	PMID:31006513	PCS		1/3			P	HPO:probinson[2023-03-16]
OMIM:607346	Spinocerebellar ataxia 19		HP:0001265	PMID:23280837	PCS		6/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0002015	PMID:23280837	PCS		7/16			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0007979	OMIM:607346	IEA					P	HPO:iea[2009-02-17]
OMIM:607346	Spinocerebellar ataxia 19		HP:0003621	PMID:23280837	PCS		1/21			C	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0002078	OMIM:607346	IEA					P	HPO:iea[2009-02-17]
OMIM:607346	Spinocerebellar ataxia 19		HP:0003596	PMID:23280837	PCS		6/21			C	HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0001272	OMIM:607346	IEA		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0002396	OMIM:607346	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:607346	Spinocerebellar ataxia 19		HP:0001260	PMID:23280837	PCS		15/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0002066	PMID:23280837	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0003584	PMID:23280837	PCS		4/21			C	HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0002174	OMIM:607346	IEA					P	HPO:iea[2009-02-17]
OMIM:607346	Spinocerebellar ataxia 19		HP:0001152	PMID:23280837	PCS		12/21			P	HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0002073	OMIM:607346	IEA					P	HPO:iea[2009-02-17]
OMIM:607346	Spinocerebellar ataxia 19		HP:0002070	OMIM:607346	IEA					P	HPO:iea[2009-02-17]
OMIM:607346	Spinocerebellar ataxia 19		HP:0100543	OMIM:607346	IEA		HP:0040283			P	HPO:probinson[2012-04-01]
OMIM:607346	Spinocerebellar ataxia 19		HP:0000639	PMID:23280837	PCS		10/19			P	HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0011462	PMID:23280837	PCS		10/21			C	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0000006	PMID:23280837	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0003677	OMIM:607346	TAS					C	HPO:skoehler[2013-11-18]
OMIM:607346	Spinocerebellar ataxia 19		HP:0001347	PMID:23280837	PCS		5/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-12]
OMIM:607346	Spinocerebellar ataxia 19		HP:0007944	OMIM:607346	IEA					P	HPO:iea[2009-02-17]
OMIM:607346	Spinocerebellar ataxia 19		HP:0001336	OMIM:607346	IEA					P	HPO:iea[2009-02-17]
OMIM:184200	SPONDYLOLISTHESIS		HP:0008489	OMIM:184200	IEA					P	HPO:iea[2009-02-17]
OMIM:184200	SPONDYLOLISTHESIS		HP:0000006	OMIM:184200	IEA					I	HPO:iea[2009-02-17]
OMIM:184200	SPONDYLOLISTHESIS		HP:0003304	OMIM:184200	IEA					P	HPO:iea[2009-02-17]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0000340	PMID:30089828	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0001561	PMID:30089828	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0006956	PMID:30089828	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0002059	PMID:30089828	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0001762	PMID:30089828	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0002365	PMID:30089828	PCS		3/4			P	HPO:skoehler[2019-02-15]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0001321	PMID:30089828	PCS		4/4			P	HPO:skoehler[2019-02-15]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0010557	PMID:30089828	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0034392	PMID:30089828	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0034197	PMID:30089828	PCS		1/4			C	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0001838	PMID:30089828	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0034198	PMID:30089828	PCS		4/4			C	HPO:probinson[2023-03-21];HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0011451	PMID:30089828	PCS		4/4			P	HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0000007	PMID:30089828	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0006872	PMID:30089828	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0001522	PMID:30089828	PCS		1/1			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-21]
OMIM:618266	Pontocerebellar hypoplasia, type 12		HP:0000347	PMID:30089828	PCS		1/4			P	HPO:skoehler[2019-02-15]
OMIM:619178	Myofibrillar myopathy 11		HP:0003687	PMID:31852522	PCS		1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003577	PMID:33217308	PCS		2/10			C	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0002015	PMID:33217308	PCS		3/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003593	PMID:33217308	PCS		1/10			C	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0001680	PMID:33217308	PCS		2/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003391	PMID:31852522	PCS		1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0012378	PMID:33217308	PCS		2/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0034635	PMID:33217308	PCS		2/8			P	HPO:probinson[2023-03-31]
OMIM:619178	Myofibrillar myopathy 11		HP:0011463	PMID:33217308	IEA		7/10			C	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0032341	PMID:31852522	PCS		1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0008981	PMID:33217308	PCS		5/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0001558	PMID:31852522	PCS	HP:0030674	1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0008872	PMID:31852522	PCS	HP:0003593	1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0025502	PMID:31852522	PCS		1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003803	PMID:33217308	PCS		6/8			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003701	PMID:33217308	PCS		9/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003327	PMID:33217308	PCS		3/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0020203	PMID:31852522	PCS		1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003724	PMID:33217308	PCS		1/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0000006	PMID:31852522	PCS					I	HPO:probinson[2021-04-30];HPO:probinson[2021-05-18]
OMIM:619178	Myofibrillar myopathy 11		HP:0001611	PMID:31852522	PCS		1/1			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003557	PMID:33217308;PMID:31852522	PCS		5/9			P	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003700	PMID:33217308	PCS		1/10			P	HPO:probinson[2021-04-30]
OMIM:619178	Myofibrillar myopathy 11		HP:0003458	PMID:33217308	PCS		5/10			P	HPO:probinson[2021-04-30]
OMIM:100100	Prune belly syndrome		HP:0001562	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0001374	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0002023	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0010957	PMID:22077972	PCS		5/5			P	HPO:skoehler[2012-10-09];HPO:probinson[2023-02-21]
OMIM:100100	Prune belly syndrome		HP:0001762	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0000072	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0030211	PMID:22077972	PCS		6/6			P	HPO:probinson[2023-02-21]
OMIM:100100	Prune belly syndrome		HP:0005199	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0004392	PMID:22077972	PCS		2/5			P	HPO:skoehler[2012-10-09];HPO:probinson[2023-02-21]
OMIM:100100	Prune belly syndrome		HP:0000767	OMIM:100100	IEA					P	HPO:skoehler[2012-10-09]
OMIM:100100	Prune belly syndrome		HP:0000217	PMID:22077972	PCS		6/6			P	HPO:skoehler[2012-10-09];HPO:probinson[2023-02-21]
OMIM:100100	Prune belly syndrome		HP:0000007	PMID:22077972	PCS					I	HPO:skoehler[2012-10-09];HPO:probinson[2023-02-21]
OMIM:100100	Prune belly syndrome		HP:0000768	OMIM:100100	IEA					P	HPO:skoehler[2012-10-09]
OMIM:100100	Prune belly syndrome		HP:0001643	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0000028	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:100100	Prune belly syndrome		HP:0000126	OMIM:100100	IEA					P	HPO:iea[2009-02-17]
OMIM:610612	Leber congenital amaurosis 12		HP:0000639	OMIM:610612	IEA					P	HPO:skoehler[2013-01-10]
OMIM:610612	Leber congenital amaurosis 12		HP:0008002	OMIM:610612	IEA					P	HPO:skoehler[2013-01-10]
OMIM:610612	Leber congenital amaurosis 12		HP:0000007	OMIM:610612	TAS					I	HPO:skoehler[2015-12-30]
OMIM:610612	Leber congenital amaurosis 12		HP:0007875	OMIM:610612	IEA	HP:0003577				P	HPO:skoehler[2013-01-09]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0001332	PMID:29392776;PMID:32467598	PCS		4/4			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0001250	PMID:32196122	PCS	HP:0003621	2/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0003593	PMID:29392776;PMID:32196122	PCS		3/3			C	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0001251	PMID:32196122	PCS		1/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0100785	PMID:32196122	PCS		1/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0000718	PMID:32196122	PCS		1/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0007166	PMID:29392776;PMID:32467598	PCS		3/3			P	HPO:probinson[2021-03-05];HPO:probinson[2021-03-05];HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0000733	PMID:32196122	PCS		2/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0002119	PMID:32196122	PCS		1/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0002311	PMID:29392776	PCS		1/1			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0008936	PMID:32467598	PCS		2/3			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0003763	PMID:32196122	PCS		1/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0000252	PMID:32196122	PCS		1/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0002353	PMID:29392776	PCS		1/1			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0000750	PMID:29392776;PMID:32196122;PMID:32467598	PCS		5/5			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0002376	PMID:32196122;PMID:32467598	PCS		3/5			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0000273	PMID:29392776	PCS		1/1		HP:0025303	P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0001263	PMID:32196122;PMID:32467598	PCS		5/5			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0002072	PMID:29392776;PMID:32467598	PCS		4/4			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0032663	PMID:32467598	PCS		1/3			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0000748	PMID:32196122	PCS		1/2			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0000007	PMID:29392776	PCS					I	HPO:probinson[2021-03-05];HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0002527	PMID:29392776;PMID:32467598	PCS		2/4			P	HPO:probinson[2021-03-05]
OMIM:619150	Intellectual developmental disorder with paroxysmal dyskinesia or seizures		HP:0007359	PMID:29392776	PCS		1/1			P	HPO:probinson[2021-03-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001397	PMID:25574476	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001771	PMID:25574476	PCS		1/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0003676	OMIM:616263	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0003577	PMID:25574476	PCS		1/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0030951	PMID:25574476	PCS		1/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0004322	OMIM:616263	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001310	PMID:25574476	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001250	OMIM:616263	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001272	PMID:25574476	PCS		2/2		HP:0003676	P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001252	PMID:25574476	PCS	HP:0003623	1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001395	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0002240	PMID:25574476	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0002460	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001251	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0003593	PMID:25574476	PCS		1/2			C	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001270	PMID:25574476	PCS		2/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000819	OMIM:616263	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0009463	PMID:25574476	PCS		1/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001508	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0009464	PMID:25574476	PCS		1/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000316	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0100807	PMID:25574476	PCS		1/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000219	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0009623	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0008897	PMID:25574476	PCS		2/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001249	OMIM:616263	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000577	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0007108	PMID:25574476	PCS		2/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000253	OMIM:616263	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0002058	PMID:25574476	PCS		2/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001265	OMIM:616263	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001762	PMID:25574476	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001263	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0002570	OMIM:616263	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0005484	PMID:25574476	PCS		2/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0011800	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0100732	PMID:25574476	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000407	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001738	PMID:25574476	PCS		2/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0002827	PMID:25574476	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000821	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0001558	PMID:25574476	PCS		1/2			P	HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000007	PMID:25574476	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000823	OMIM:616263	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000248	PMID:25574476	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:616263	Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset		HP:0000049	PMID:25574476	PCS		1/1	MALE		P	HPO:skoehler[2015-04-05];HPO:probinson[2023-03-22]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002366	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0003236	PMID:9837826	PCS		7/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0030237	PMID:19344878	PCS		20/24			P	HPO:probinson[2022-03-14]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0003596	PMID:9837826	PCS		10/12			C	HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002483	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002460	PMID:9837826	PCS		12/12			P	HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0001609	OMIM:606070	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0011462	PMID:9837826	PCS		2/12			C	HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002936	OMIM:606070	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0003805	PMID:9837826	PCS		5/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002835	OMIM:606070	IEA					P	HPO:iea[2009-02-17]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0008756	OMIM:606070	IEA					P	HPO:iea[2009-02-17]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0003547	PMID:19344878;PMID:9837826	PCS		12/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-06-03];HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0001347	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002015	PMID:19344878	PCS		13/19			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0003687	PMID:9837826	PCS		3/6			P	HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0001283	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0001260	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0003581	OMIM:606070;PMID:19344878	PCS		34/34			C	HPO:probinson[2013-12-15];HPO:probinson[2022-03-14]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0009053	PMID:19344878	PCS		23/24			P	HPO:probinson[2022-03-14]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0000726	OMIM:606070	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0007354	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002747	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0000762	PMID:9837826	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-03]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0000006	PMID:19344878	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0002127	OMIM:606070	TAS					P	HPO:skoehler[2014-05-04]
OMIM:606070	Amyotrophic lateral sclerosis 21		HP:0003557	PMID:19344878	PCS		1/1			P	HPO:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001771	PMID:15691357;PMID:10939567	PCS		40/42			P	ORCID:0000-0002-0736-9199[2024-11-05];HPO:iea[2009-02-17];HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003236	PMID:10939567	PCS		13/13			P	HPO:probinson[2012-04-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003596	PMID:10939567	PCS		2/40			C	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003551	PMID:10939567	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003273	PMID:10939567	PCS		13/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003391	PMID:10939567	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0012664	PMID:15691357	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0009060	PMID:10939567	PCS		10/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0011463	PMID:10939567	PCS		25/40			C	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003707	PMID:10939567	PCS		3/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0011462	PMID:10939567	PCS		1/40			C	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0009027	PMID:15691357	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003307	PMID:10939567	PCS		1/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0007126	PMID:10939567	PCS		3/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003306	PMID:10939567	PCS		36/40			P	HPO:iea[2009-02-17]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001645	OMIM:181350	TAS					P	HPO:skoehler[2013-01-22]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001644	OMIM:181350	IEA					P	HPO:iea[2009-02-17]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003700	PMID:10939567	PCS		3/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003623	PMID:10939567	PCS		1/40			C	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0008959	PMID:10939567	PCS		17/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0025258	PMID:10939567	PCS		36/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0011727	PMID:15691357	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0012378	PMID:10939567	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0009053	PMID:10939567	PCS		21/40			P	HPO:probinson[2012-04-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0034671	PMID:10939567	PCS		4/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0006785	PMID:10939567	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0002505	PMID:10939567	PCS		4/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0002942	PMID:10939567	PCS		1/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0000006	PMID:10939567	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0034391	PMID:10939567	PCS		39/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003677	PMID:10939567	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0005997	OMIM:181350	IEA					P	HPO:iea[2009-02-17]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003697	PMID:10939567	PCS		13/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0031329	PMID:15691357	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003693	PMID:10939567	PCS		3/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0030234	PMID:10939567	PCS		16/31			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003691	PMID:10939567	PCS		1/41			P	HPO:skoehler[2012-10-17]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0011711	PMID:15691357	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003690	PMID:10939567	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0011675	PMID:10939567;OMIM:181350	PCS		33/33			P	ORCID:0000-0002-0736-9199[2024-11-05];HPO:probinson[2012-04-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0034681	PMID:10939567	PCS		2/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0009046	PMID:10939567	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0009049	PMID:15691357	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0002515	PMID:10939567	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0002359	PMID:10939567	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0009129	PMID:10939567	PCS		7/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003325	PMID:15691357	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0002875	PMID:15691357	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0003621	PMID:10939567	PCS		11/40			C	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0004631	OMIM:181350	IEA					P	HPO:iea[2009-02-17]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0002650	PMID:10939567	PCS		5/40			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001762	PMID:10939567	PCS		3/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001288	PMID:10939567	PCS		18/18			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001761	PMID:10939567	PCS		2/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0011705	PMID:15691357	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0005162	PMID:10939567	PCS		9/36			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0008180	OMIM:181350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0025708	PMID:15691357	PCS		1/1			C	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0007210	PMID:10939567	PCS		7/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001239	PMID:10939567	PCS		3/41			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0004308	PMID:10939567	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-11-05]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0001279	PMID:15691357	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:181350	Emery-Dreifuss muscular dystrophy 2, autosomal dominant		HP:0008944	OMIM:181350	TAS					P	HPO:probinson[2012-04-11]
OMIM:614474	Atrioventricular septal defect 5		HP:0003577	PMID:20581743	PCS		1/1			C	HPO:probinson[2022-10-11]
OMIM:614474	Atrioventricular septal defect 5		HP:0004383	PMID:20581743	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:614474	Atrioventricular septal defect 5		HP:0006695	PMID:20581743	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-11]
OMIM:614474	Atrioventricular septal defect 5		HP:0000006	PMID:20581743	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-11]
OMIM:614474	Atrioventricular septal defect 5		HP:0011623	PMID:20581743	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-10-11]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0002066	PMID:15918153	PCS					P	HPO:iea[2009-02-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0001508	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000718	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000717	PMID:15918153	PCS					P	HPO:iea[2009-02-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000739	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000733	PMID:15918153	PCS					P	HPO:iea[2010-09-13]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0100807	PMID:15918153	PCS					P	HPO:probinson[2013-04-09]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000219	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0003745	OMIM:609425	IEA					I	HPO:iea[2009-02-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000752	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000358	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0001249	PMID:15918153	PCS					P	HPO:probinson[2013-04-09]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000275	PMID:15918153	PCS					P	HPO:iea[2012-05-01]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000252	PMID:15918153	PCS					P	HPO:iea[2010-09-13]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000276	PMID:15918153	PCS					P	HPO:iea[2012-05-01]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0001263	PMID:15918153	PCS	HP:0003593				P	HPO:iea[2010-09-13]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0001182	PMID:15918153	PCS					P	HPO:probinson[2013-04-09]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000709	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0001518	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000426	PMID:15918153	PCS					P	HPO:iea[2009-02-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000767	PMID:15918153	PCS					P	HPO:iea[2009-02-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000768	PMID:15918153	PCS					P	HPO:iea[2009-02-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0004209	PMID:15918153	PCS					P	HPO:iea[2010-09-13]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000400	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000322	PMID:15918153	PCS					P	HPO:iea[2009-02-17]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000006	OMIM:609425	IEA					I	HPO:iea[2010-09-13]
OMIM:609425	Chromosome 3q29 deletion syndrome		HP:0000369	OMIM:609425	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619636	Acromesomelic dysplasia 4		HP:0006009	PMID:33106379	PCS		2/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0003015	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0008905	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0004322	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0003498	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0001252	PMID:34782440	PCS		0/1			P	HPO:probinson[2022-02-02];HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0003031	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0003890	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0010049	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0010743	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0009381	PMID:34782440;PMID:33106379	PCS		3/3			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0001709	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0011463	PMID:34782440	PCS		1/1			C	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0012450	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0002938	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000998	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0002857	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0001500	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0009803	PMID:33106379	PCS		2/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0003027	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000431	PMID:34782440;PMID:33106379	PCS		2/3			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000574	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0002970	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0003025	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0002230	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0004592	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0001837	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000926	PMID:34782440;PMID:33106379	PCS		3/3			P	HPO:probinson[2022-02-02];HPO:probinson[2022-02-02];HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0001537	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000007	PMID:34782440	PCS					I	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000920	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000307	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000664	PMID:34782440;PMID:33106379	PCS		2/3			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0005616	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0002986	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000884	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0001852	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0002943	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000303	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000369	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0000325	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0001831	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619636	Acromesomelic dysplasia 4		HP:0004568	PMID:33106379	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000341	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0003477	PMID:26168012	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001276	PMID:26168012	PCS		3/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0010804	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000189	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0003376	OMIM:616505	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000463	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001310	PMID:26168012	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001272	PMID:26168012	PCS		1/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001371	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0003693	PMID:26168012	PCS		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0002066	PMID:26168012	PCS		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001252	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001251	PMID:26168012	PCS		3/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001290	OMIM:616505	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0002080	PMID:26168012	PCS		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000639	PMID:26168012	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0003828	OMIM:616505	TAS					M	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000414	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0002936	OMIM:616505	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0002878	OMIM:616505	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001324	OMIM:616505	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000575	PMID:26168012	PCS		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000577	OMIM:616505	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001347	PMID:26168012	PCS		1/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001265	OMIM:616505	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0002135	PMID:26168012	IEA		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0002650	OMIM:616505	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000750	PMID:26168012	PCS		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0003487	PMID:26168012	PCS		1/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001761	PMID:26168012	PCS		1/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001263	PMID:26168012	PCS		3/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0003186	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001284	PMID:26168012	PCS		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001182	OMIM:616505	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0012698	PMID:26168012	PCS		1/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000529	OMIM:616505	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000007	PMID:26168012	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-26]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000648	PMID:26168012	PCS		3/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0000505	PMID:26168012	PCS		3/6			P	HPO:probinson[2021-07-03]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001337	OMIM:616505	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616505	Neuropathy, hereditary motor and sensory, type VIB		HP:0001336	OMIM:616505	IEA					P	HPO:skoehler[2018-10-08]
OMIM:185650	Symphalangism, c. s. Lewis type		HP:0000006	OMIM:185650	TAS					I	HPO:probinson[2009-02-17]
OMIM:185650	Symphalangism, c. s. Lewis type		HP:0009703	OMIM:185650	TAS					P	HPO:probinson[2009-02-17]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0031956	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0001396	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0002079	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0000463	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0002153	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0003573	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0002151	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0003593	PMID:27592148	PCS		1/1			C	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0002240	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0003073	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0003270	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0005280	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0033725	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0031964	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0002908	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0009141	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0006581	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0000007	PMID:27592148	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0001942	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0000952	PMID:27592148	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0004448	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:618528	Mitochondrial DNA depletion syndrome 16 (hepatic type)		HP:0001414	PMID:27592148	PCS		1/1			P	HPO:probinson[2023-06-09]
OMIM:616511	Maturity-onset diabetes of the young, type 14		HP:0000819	PMID:26073777	PCS					P	HPO:skoehler[2015-08-16];HPO:probinson[2023-03-05]
OMIM:616511	Maturity-onset diabetes of the young, type 14		HP:0003596	PMID:26073777	PCS		6/13			C	HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:616511	Maturity-onset diabetes of the young, type 14		HP:0011462	PMID:26073777	PCS		7/13			C	HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:616511	Maturity-onset diabetes of the young, type 14		HP:0004904	PMID:26073777	PCS		13/13			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-05]
OMIM:616511	Maturity-onset diabetes of the young, type 14		HP:0040217	PMID:26073777	PCS		5/13			P	HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:616511	Maturity-onset diabetes of the young, type 14		HP:0000006	PMID:26073777	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-05]
OMIM:600373	CODAS syndrome		HP:0002663	PMID:25808063	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001374	PMID:28148925;PMID:25808063	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-06-13];HPO:iea[2009-02-17];HPO:probinson[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0003112	PMID:28148925	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0002023	PMID:28148925;PMID:25574826;PMID:25808063	PCS		3/12			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0000684	PMID:25574826;PMID:25808063	PCS		3/7			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0003311	PMID:25574826	PCS		2/2			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0004322	PMID:28148925;PMID:25574826;PMID:25808063	PCS		7/12			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0002340	PMID:28148925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001250	PMID:25574826	PCS		1/4			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0001252	PMID:28148925;PMID:25808063	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-06-13];HPO:iea[2009-02-17];HPO:probinson[2024-06-13]
OMIM:600373	CODAS syndrome		HP:6000870	PMID:25808063	PCS					P	HPO:probinson[2024-08-03]
OMIM:600373	CODAS syndrome		HP:0001251	PMID:25808063	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0002020	PMID:25574826	PCS		2/4			P	HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0003593	PMID:25808063	PCS		4/7			C	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001290	PMID:25574826	PCS		4/4			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0002061	PMID:28148925;PMID:25808063	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0010049	OMIM:600373	IEA					P	HPO:iea[2009-02-17]
OMIM:600373	CODAS syndrome		HP:0100255	PMID:25574826	PCS		4/4			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0000518	PMID:25574826;PMID:25808063	PCS		11/11			P	HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0000519	OMIM:600373	IEA					P	HPO:iea[2009-02-17]
OMIM:600373	CODAS syndrome		HP:0009623	OMIM:600373	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:600373	CODAS syndrome		HP:0002857	PMID:25574826;PMID:25808063	PCS		9/10			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001604	PMID:25574826	PCS		3/4			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0001249	PMID:25574826;PMID:25808063	PCS		6/9			P	HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001601	PMID:25808063	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0009901	PMID:25574826;PMID:25808063	PCS		8/11			P	HP:probinson[2019-03-01];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001266	PMID:28148925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0002750	OMIM:600373	IEA					P	HPO:iea[2009-02-17]
OMIM:600373	CODAS syndrome		HP:0002079	OMIM:600373	TAS					P	HPO:skoehler[2015-02-22]
OMIM:600373	CODAS syndrome		HP:0001263	PMID:28148925;PMID:25808063	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-06-13];HPO:iea[2009-02-17];HPO:probinson[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0008081	PMID:25574826	PCS		2/2			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0000407	PMID:25574826;PMID:25808063	PCS		2/11			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001537	PMID:25808063	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0000007	PMID:25574826	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0001539	PMID:25574826	PCS		1/4			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0000405	PMID:25574826;PMID:25808063	PCS		3/10			P	HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001216	OMIM:600373	IEA					P	HPO:iea[2009-02-17]
OMIM:600373	CODAS syndrome		HP:0001655	PMID:25808063	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0000143	PMID:28148925;PMID:25574826;PMID:25808063	PCS		2/10			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0003577	PMID:28148925;PMID:25808063	PCS		4/8			C	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0000463	PMID:25574826	PCS		4/4			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0002761	OMIM:600373	IEA					P	HPO:skoehler[2019-02-22]
OMIM:600373	CODAS syndrome		HP:0002682	OMIM:600373	TAS					P	HPO:skoehler[2015-02-22]
OMIM:600373	CODAS syndrome		HP:0003177	OMIM:600373	IEA					P	HPO:iea[2009-02-17]
OMIM:600373	CODAS syndrome		HP:0005792	OMIM:600373	IEA					P	HPO:iea[2009-02-17]
OMIM:600373	CODAS syndrome		HP:0001270	PMID:28148925;PMID:25574826;PMID:25808063	PCS		10/11			P	HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0012368	PMID:25808063	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001629	OMIM:600373	TAS					P	HPO:skoehler[2015-02-22]
OMIM:600373	CODAS syndrome		HP:0006297	PMID:25574826	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0006695	OMIM:600373	TAS					P	HPO:skoehler[2015-02-22]
OMIM:600373	CODAS syndrome		HP:0008278	PMID:28148925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0002119	OMIM:600373	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600373	CODAS syndrome		HP:0009803	OMIM:600373	IEA					P	HPO:iea[2009-02-17]
OMIM:600373	CODAS syndrome		HP:0002015	PMID:28148925;PMID:25808063	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0001561	OMIM:600373	TAS					P	HPO:skoehler[2015-02-22]
OMIM:600373	CODAS syndrome		HP:0002650	PMID:25574826	PCS		4/4			P	HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0001321	PMID:25808063	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0003542	PMID:28148925	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0010818	PMID:28148925;PMID:25808063	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0010577	OMIM:600373	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600373	CODAS syndrome		HP:0005280	OMIM:600373	TAS					P	HPO:skoehler[2015-02-22]
OMIM:600373	CODAS syndrome		HP:0000508	PMID:25574826	PCS		4/4			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0003417	PMID:25574826;PMID:25808063	PCS		4/9			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0009556	PMID:25808063	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:600373	CODAS syndrome		HP:0004626	OMIM:600373	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600373	CODAS syndrome		HP:0001631	PMID:25574826	PCS		2/4			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:600373	CODAS syndrome		HP:0000028	PMID:25574826	PCS		1/2			P	HPO:skoehler[2015-02-22];HP:probinson[2019-03-01]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001561	PMID:28702509	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0000750	PMID:28702509	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0000640	PMID:16236810	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0000486	PMID:16236810	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001310	PMID:28702509	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001272	PMID:16236810	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001260	PMID:28702509	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0025312	PMID:16236810	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0002066	PMID:28702509	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001263	PMID:28702509;PMID:16236810	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001252	PMID:28702509;PMID:16236810	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001251	PMID:16236810	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001290	OMIM:614306	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0025162	PMID:28702509	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0000609	PMID:16236810	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0011463	PMID:28702509	PCS		1/2			C	HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0000646	PMID:16236810	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0007018	PMID:28702509;PMID:16236810	PCS		2/3			P	HPO:probinson[2022-08-27];HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0000006	PMID:16236810	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0001249	PMID:16236810	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-27]
OMIM:614306	Cognitive impairment with or without cerebellar ataxia		HP:0003623	PMID:28702509	PCS		1/2			C	HPO:probinson[2022-08-27]
OMIM:608049	Autism, susceptibility to, 3		HP:0000750	OMIM:608049	IEA					P	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0002353	OMIM:608049	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0001250	OMIM:608049	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0003144	OMIM:608049	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0002919	OMIM:608049	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608049	Autism, susceptibility to, 3		HP:0011463	OMIM:608049	IEA					C	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0000717	OMIM:608049	TAS					P	HPO:probinson[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0000728	OMIM:608049	IEA					P	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0000723	OMIM:608049	TAS					P	HPO:skoehler[2013-06-04]
OMIM:608049	Autism, susceptibility to, 3		HP:0001426	OMIM:608049	IEA					I	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0000733	OMIM:608049	TAS					P	HPO:probinson[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0000758	OMIM:608049	TAS					P	HPO:probinson[2012-07-16]
OMIM:608049	Autism, susceptibility to, 3		HP:0003745	OMIM:608049	IEA					I	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0000732	OMIM:608049	IEA					P	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0001249	OMIM:608049	IEA					P	HPO:iea[2009-02-17]
OMIM:608049	Autism, susceptibility to, 3		HP:0000721	OMIM:608049	IEA					P	HPO:iea[2009-02-17]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0002465	PMID:25753423	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000750	PMID:25753423	PCS		2/2		HP:0012828	P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000189	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000431	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000276	PMID:25753423	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0001156	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0001250	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0001263	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0003593	PMID:25753423	PCS		2/2			C	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0004482	PMID:25753423	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0002392	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0011463	PMID:33161245	PCS		1/1			C	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000448	PMID:25753423	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000007	PMID:25753423	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000752	PMID:25753423	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000268	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000256	PMID:33161245	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0000303	PMID:25753423	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:617169	Intellectual developmental disorder, autosomal recessive 74		HP:0001249	PMID:25753423;PMID:33161245	PCS		3/3			P	HPO:probinson[2022-03-07];HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:619144	Spermatogenic failure 49		HP:0032560	PMID:32791035	PCS		5/5			P	HPO:probinson[2021-01-08]
OMIM:619144	Spermatogenic failure 49		HP:0003251	PMID:32791035	PCS		5/5			P	HPO:probinson[2021-01-08]
OMIM:619144	Spermatogenic failure 49		HP:0003581	PMID:32791035	PCS					C	HPO:probinson[2021-01-08]
OMIM:619144	Spermatogenic failure 49		HP:0000007	PMID:32791035	PCS					I	HPO:probinson[2021-01-08];HPO:probinson[2021-01-08]
OMIM:619144	Spermatogenic failure 49		HP:0012207	PMID:32791035	PCS		5/5			P	HPO:probinson[2021-01-08]
OMIM:619144	Spermatogenic failure 49		HP:0032558	PMID:32791035	PCS		5/5			P	HPO:probinson[2021-01-08]
OMIM:619144	Spermatogenic failure 49		HP:0032559	PMID:32791035	PCS		5/5			P	HPO:probinson[2021-01-08]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0003577	PMID:25125611	PCS		2/2			C	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0000365	OMIM:616277	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001332	OMIM:616277	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001252	OMIM:616277	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0012707	PMID:25125611	PCS		2/2			P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0010544	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001290	PMID:25125611	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0012444	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0033725	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001629	PMID:25125611	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0000639	OMIM:616277	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0007366	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0002878	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001522	PMID:25125611	PCS		2/2			C	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001662	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0011968	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0002033	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0002151	PMID:25125611	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001263	OMIM:616277	TAS				HP:0012828	P	HPO:skoehler[2015-04-05]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0002490	PMID:25125611	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:6000469	PMID:29575569	PCS		4/4			P	HPO:probinson[2024-04-03]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0011344	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0002928	PMID:25125611	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001639	PMID:25125611	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0000007	PMID:25125611	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-26]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0001257	OMIM:616277	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616277	Mitochondrial short-chain enoyl-coa hydratase 1 deficiency		HP:0002104	PMID:25125611	PCS		2/2		HP:0025303	P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-26]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0005599	PMID:33878481	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000083	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0002583	OMIM:203300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0001010	PMID:33878481	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0003010	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0031364	PMID:33878481	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000639	PMID:33878481	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000618	OMIM:203300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000613	PMID:33878481	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0001107	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000978	PMID:33878481	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000995	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0007603	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0002037	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0001022	OMIM:203300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0002573	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0001480	OMIM:203300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0001141	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0002091	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000007	OMIM:203300	IEA					I	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0001638	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0002206	OMIM:203300	TAS					P	HPO:skoehler[2010-06-20]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000421	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0002027	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:203300	Hermansky-Pudlak syndrome 1		HP:0000225	OMIM:203300	IEA					P	HPO:iea[2009-02-17]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0000252	PMID:27677260	PCS		0/3			P	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0000750	PMID:27523599;PMID:27677260	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001344	PMID:27523599	PCS		2/5			P	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001662	PMID:27523599	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0011704	PMID:27523599	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001250	PMID:27523599	PCS		4/9			P	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001263	PMID:27523599	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001252	PMID:27523599	PCS		6/9			P	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0002020	PMID:27523599	PCS		5/8			P	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0003593	PMID:27523599	PCS		9/9			C	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001270	PMID:27677260	PCS		3/5			P	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0000639	PMID:27523599	PCS		6/7			P	HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0007010	PMID:27523599	PCS		1/9			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0000007	PMID:27523599	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0000752	PMID:27677260	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0007018	PMID:27677260	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001249	PMID:27523599;PMID:27677260	PCS		9/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11];HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:617182	Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia		HP:0001655	PMID:27523599	PCS		1/8			P	HPO:probinson[2022-10-11]
OMIM:207600	Takayasu arteritis		HP:0012089	OMIM:207600	TAS					P	HPO:probinson[2013-01-07]
OMIM:207600	Takayasu arteritis		HP:0000007	OMIM:207600	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:601086	Laterality defects, autosomal dominant		HP:0030853	OMIM:601086	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601086	Laterality defects, autosomal dominant		HP:0001696	OMIM:601086	IEA					P	HPO:iea[2009-02-17]
OMIM:601086	Laterality defects, autosomal dominant		HP:0001507	OMIM:601086	IEA					P	HPO:iea[2009-02-17]
OMIM:601086	Laterality defects, autosomal dominant		HP:0001746	OMIM:601086	IEA					P	HPO:iea[2009-02-17]
OMIM:601086	Laterality defects, autosomal dominant		HP:0000006	OMIM:601086	IEA					I	HPO:iea[2009-02-17]
OMIM:619805	Spermatogenic failure 68		HP:0003251	PMID:31985809	PCS		1/1			P	HPO:probinson[2022-05-04]
OMIM:619805	Spermatogenic failure 68		HP:0011462	PMID:31985809	PCS		1/1			C	HPO:probinson[2022-05-04]
OMIM:619805	Spermatogenic failure 68		HP:0000007	PMID:31985809	PCS					I	HPO:probinson[2024-08-03]
OMIM:619805	Spermatogenic failure 68		HP:0012205	PMID:31985809	PCS		1/1			P	HPO:probinson[2022-05-04]
OMIM:179400	Radius, aplasia of, with cleft lip/palate		HP:0000175	OMIM:179400	TAS					P	HPO:skoehler[2013-12-15]
OMIM:179400	Radius, aplasia of, with cleft lip/palate		HP:0000204	OMIM:179400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:179400	Radius, aplasia of, with cleft lip/palate		HP:0003974	OMIM:179400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608908	Myopia 6		HP:0003202	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0000365	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001250	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001098	PMID:25525168	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001252	PMID:23643385	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001251	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001270	PMID:23643385	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0011003	PMID:23643385;PMID:25525168	PCS		6/6			P	HPO:probinson[2022-10-18];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001508	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0011463	PMID:25525168	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001635	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0007663	PMID:25525168	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0002878	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001324	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0000006	PMID:23643385	PCS					I	HPO:skoehler[2013-07-30];HPO:probinson[2022-10-18]
OMIM:608908	Myopia 6		HP:0007800	PMID:25525168	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:608908	Myopia 6		HP:0001249	PMID:23643385;PMID:25525168	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:134500	Factor VIII deficiency		HP:0001892	OMIM:134500	IEA					P	HPO:iea[2009-02-17]
OMIM:134500	Factor VIII deficiency		HP:0003125	OMIM:134500	IEA					P	HPO:iea[2009-02-17]
OMIM:134500	Factor VIII deficiency		HP:0000006	OMIM:134500	IEA					I	HPO:iea[2009-02-17]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0000099	PMID:20237408	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0003774	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0410295	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0011839	PMID:20237408	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0002240	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0032134	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0012587	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0010975	PMID:20237408	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0033295	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0012476	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0002829	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0000979	PMID:20237408	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0012593	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0002718	OMIM:613496	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0000007	PMID:20237408	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0001973	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0002205	PMID:20237408	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0000105	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613496	Immunodeficiency, common variable, 6		HP:0000126	PMID:20237408	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:615959	Centronuclear myopathy 5		HP:0008936	PMID:25087613	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0003687	PMID:25087613	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0000160	PMID:25087613	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0000193	PMID:25087613	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0003273	PMID:25087613	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0003593	PMID:25087613	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0001284	PMID:25087613	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0001290	PMID:25087613	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0001270	PMID:25087613	PCS		3/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0002093	PMID:25087613	PCS				HP:0012828	P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0030319	PMID:25087613	PCS		2/3			P	HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0040081	PMID:25087613	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0000602	PMID:25087613	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0000007	PMID:25087613	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0000218	PMID:25087613	PCS		3/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0003701	PMID:25087613	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0003327	OMIM:615959	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615959	Centronuclear myopathy 5		HP:0001324	PMID:25087613	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0000278	PMID:25087613	PCS		2/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0001653	PMID:25087613	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0000347	PMID:25087613	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:615959	Centronuclear myopathy 5		HP:0001644	PMID:25087613	PCS		2/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-05]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000286	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0008947	PMID:9557891	PCS					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001058	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000023	PMID:9557891	PCS					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0004322	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0002783	PMID:4023980	PCS		5/10			P	HPO:probinson[2021-01-26]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001030	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001073	PMID:9557891;OMIM:130000	IEA		20/20			P	HPO:probinson[2017-06-16];HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001373	OMIM:130000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0010500	PMID:9557891	PCS					P	HPO:probinson[2017-06-16]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0002616	PMID:12180144	PCS		14/42			P	HPO:iea[2009-02-17];HP:probinson[2019-05-11]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000978	PMID:9557891	PCS					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0002758	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000977	PMID:9557891	PCS					P	HPO:skoehler[2010-06-18]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001763	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000993	PMID:9557891;PMID:9557891	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-01-11]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000974	PMID:9557891	PCS					P	HPO:probinson[2017-06-16]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0006316	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001187	PMID:9557891	PCS					P	HPO:probinson[2017-06-16]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001382	PMID:9557891	PCS					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0002010	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0005222	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000592	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000394	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0005100	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0025014	PMID:9557891	PCS					P	HPO:probinson[2017-06-16]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001083	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0011108	PMID:4023980	PCS		3/10			P	HPO:probinson[2021-01-26]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0010485	PMID:9557891	PCS					P	HPO:probinson[2017-06-16]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001537	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000767	PMID:4023980	PCS		2/10			P	HPO:probinson[2021-01-26]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000006	PMID:9557891	PCS					I	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0001634	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0000545	OMIM:130000	IEA					P	HPO:iea[2009-02-17]
OMIM:130000	Ehlers-danlos syndrome, type I		HP:0002105	PMID:4023980	PCS		1/10			P	HPO:probinson[2021-01-26]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0001012	PMID:8734663	PCS					P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0030436	PMID:18234728	PCS		75/89			P	HPO:skoehler[2015-08-05];HP:probinson[2019-01-25]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0003003	PMID:18234728	PCS		2/51			P	HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0030255	PMID:9835964	PCS					P	HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0005584	PMID:18234728	PCS		30/51			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0032227	PMID:18234728	PCS		4/51			P	HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0032228	PMID:18234728	PCS		9/51			P	HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0000107	OMIM:135150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0002108	PMID:18234728	IEA		27/51			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0007620	PMID:18234728	PCS		1/51			P	HP:probinson[2019-03-02]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0005948	PMID:28830849	PCS					P	HPO:probinson[2019-04-20]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0000006	PMID:18234728	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-01-25]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0009726	OMIM:135150	IEA					P	HPO:iea[2009-02-17]
OMIM:135150	Birt-Hogg-Dube syndrome		HP:0006755	PMID:18234728	PCS		1/51			P	HP:probinson[2019-03-02]
OMIM:300147	Prostate cancer, hereditary, X-linked 1		HP:0001417	OMIM:300147	IEA					I	HPO:skoehler[2013-01-11]
OMIM:300147	Prostate cancer, hereditary, X-linked 1		HP:0012125	OMIM:300147	IEA					P	HPO:skoehler[2013-01-09]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0003577	PMID:38141607	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0001162	PMID:38141607	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0001195	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0001263	PMID:38141607	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0004592	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000518	PMID:38141607	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000729	PMID:38141607	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000568	PMID:38141607	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0002119	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000768	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0001830	PMID:38141607	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0001631	PMID:38141607	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000047	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000256	PMID:38141607	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0009789	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0007898	PMID:38141607	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000567	PMID:38141607	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000006	PMID:38141607	PCS					I	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0000104	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620712	Polydactyly-macrocephaly syndrome		HP:0001655	PMID:38141607	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:146800	Ichthyosis, Bullous type		HP:0007475	OMIM:146800	TAS					P	HPO:probinson[2013-03-24]
OMIM:146800	Ichthyosis, Bullous type		HP:0000006	OMIM:146800	IEA					I	HPO:probinson[2009-02-17]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0000473	PMID:23424103	PCS		6/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0000275	OMIM:128101	TAS					P	HPO:skoehler[2013-07-17]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0002015	PMID:23424103	PCS		2/8			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0003621	PMID:23424103	PCS		3/8			C	HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0009938	OMIM:128101	TAS					P	HPO:skoehler[2014-05-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0002451	PMID:23424103	PCS		2/8			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0002066	OMIM:128101	TAS					P	HPO:skoehler[2014-05-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0032005	PMID:23424103	PCS		1/8			P	HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0001618	PMID:23424103	PCS		6/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0011462	PMID:23424103	PCS		5/8			C	HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0007325	PMID:23424103	PCS					P	HPO:skoehler[2013-07-17];HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0001533	OMIM:128101	IEA					P	HPO:skoehler[2019-04-18]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0000006	PMID:23424103	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-24]
OMIM:128101	Dystonia 4, torsion, autosomal dominant		HP:0001304	PMID:23424103	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-24]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0004325	PMID:29036432	PCS		2/2			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0000252	PMID:29036432	PCS		2/2			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0003676	PMID:29036432	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0003577	PMID:29036432	PCS		2/2			C	HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0001531	PMID:29036432	PCS		2/2			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0000002	PMID:29036432	PCS		0/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0002188	PMID:29036432	PCS		2/2			P	HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0002079	PMID:29036432	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0011344	PMID:29036432	PCS		2/2			P	HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0012510	PMID:29036432	PCS		2/2			P	HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0100704	PMID:29036432	PCS		2/2			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0000007	PMID:29036432	PCS					I	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0002119	PMID:29036432	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0001257	PMID:29036432	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-22]
OMIM:617800	Microcephaly 19, primary, autosomal recessive		HP:0009879	PMID:29036432	PCS		2/2			P	HPO:nvasilevsky[2019-02-26];HPO:probinson[2022-06-22]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0004313	PMID:20489057	PCS					P	HPO:probinson[2013-01-09]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0002037	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0002155	PMID:20489057	PCS		7/8			P	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0002583	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001581	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0002240	OMIM:300635	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0011900	PMID:20489057	PCS		7/8			P	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001061	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0012219	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0003281	PMID:20489057	PCS		7/8			P	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0012115	PMID:20489057	PCS		8/9			P	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0025084	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0012156	PMID:20489057	PCS		4/9			P	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001915	OMIM:300635	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0002719	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001419	OMIM:300635	IEA					I	HPO:skoehler[2019-04-18]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001954	OMIM:300635	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001945	PMID:20489057	PCS		9/10			P	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001417	PMID:20489057	PCS					I	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0002205	OMIM:300635	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001744	PMID:20489057	PCS		9/10			P	HPO:probinson[2013-02-17]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0001876	OMIM:300635	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:300635	Lymphoproliferative syndrome, X-linked, 2		HP:0002721	OMIM:300635	IEA					P	HPO:skoehler[2018-10-08]
OMIM:302803	Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia		HP:0001419	OMIM:302803	TAS					I	HPO:probinson[2012-04-18]
OMIM:302803	Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia		HP:0007385	OMIM:302803	TAS					P	HPO:probinson[2012-04-18]
OMIM:302803	Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia		HP:0001362	OMIM:302803	TAS		3/3			P	HPO:probinson[2012-04-18]
OMIM:302803	Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia		HP:0007002	OMIM:302803	TAS					P	HPO:probinson[2012-03-12]
OMIM:302803	Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia		HP:0003390	OMIM:302803	TAS					P	HPO:probinson[2012-03-12]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0001155	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002167	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002186	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002340	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0001250	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000020	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0010524	OMIM:221770	IEA					P	HPO:skoehler[2010-06-18]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0031844	OMIM:221770	IEA					P	HPO:skoehler[2018-10-08]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000719	OMIM:221770	IEA					P	HPO:skoehler[2018-10-08]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000718	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0011462	PMID:12370476	PCS		6/6			C	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000734	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000757	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002756	OMIM:221770	TAS					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000751	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0003447	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0001760	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002135	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002476	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002059	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0006956	PMID:12370476	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002353	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0003487	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0001288	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002079	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002354	OMIM:221770	IEA					P	HPO:skoehler[2010-06-20]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002352	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002171	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0011096	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0012062	PMID:12370476	PCS		6/6			P	HPO:probinson[2015-03-22];HPO:probinson[2022-04-30]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000727	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000726	PMID:12370476	PCS	HP:0011462	6/6			P	HPO:probinson[2022-04-30]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0000007	PMID:10888890	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-04-30]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0001257	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0002127	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:221770	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy		HP:0001336	OMIM:221770	IEA					P	HPO:iea[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0000343	PMID:25945256	PCS		1/3			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-06]
OMIM:273750	3-M syndrome 1		HP:0000463	OMIM:273750	TAS					P	HPO:skoehler[2010-06-18]
OMIM:273750	3-M syndrome 1		HP:0004322	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0003298	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0001373	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0003691	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0010306	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0008897	OMIM:273750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:273750	3-M syndrome 1		HP:0003307	PMID:25945256	PCS		1/3			P	HPO:probinson[2012-07-30];HPO:probinson[2021-07-06]
OMIM:273750	3-M syndrome 1		HP:0008734	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0001763	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0000773	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0000179	OMIM:273750	IEA					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0001249	PMID:25945256	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:273750	3-M syndrome 1		HP:0008839	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0000574	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0002750	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0001382	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0003100	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0000272	OMIM:273750	TAS					P	HPO:skoehler[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0000470	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0004570	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0005280	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0001518	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0002827	OMIM:273750	TAS					P	HPO:probinson[2012-07-30]
OMIM:273750	3-M syndrome 1		HP:0000767	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0000007	PMID:16142236	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-07-06]
OMIM:273750	3-M syndrome 1		HP:0000307	PMID:25945256	PCS		1/3			P	HPO:probinson[2012-07-30];HPO:probinson[2021-07-06]
OMIM:273750	3-M syndrome 1		HP:0004209	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0009237	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0000268	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0002007	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0001511	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0001511	PMID:25945256	PCS	HP:0003577	4/4			P	HPO:probinson[2021-07-06]
OMIM:273750	3-M syndrome 1		HP:0000047	OMIM:273750	TAS					P	HPO:probinson[2009-02-17]
OMIM:273750	3-M syndrome 1		HP:0001510	PMID:25945256	PCS		4/4			P	HPO:probinson[2021-07-06]
OMIM:273750	3-M syndrome 1		HP:0000303	OMIM:273750	TAS					P	HPO:skoehler[2010-06-20]
OMIM:273750	3-M syndrome 1		HP:0002643	OMIM:273750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:273750	3-M syndrome 1		HP:0000325	PMID:25945256	PCS		2/3			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-06]
OMIM:617035	Patent ductus arteriosus 2		HP:0003577	PMID:18752453	PCS		6/6			C	HPO:probinson[2022-09-12]
OMIM:617035	Patent ductus arteriosus 2		HP:0004209	PMID:18752453	PCS		0/6			P	HPO:probinson[2022-09-12]
OMIM:617035	Patent ductus arteriosus 2		HP:0001643	PMID:18752453	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-12]
OMIM:617035	Patent ductus arteriosus 2		HP:0000006	PMID:18752453	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-12]
OMIM:620699	Maple syrup urine disease, type II		HP:0001254	PMID:9621512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-16]
OMIM:620699	Maple syrup urine disease, type II		HP:0002179	PMID:9621512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-16]
OMIM:620699	Maple syrup urine disease, type II		HP:0001993	PMID:9621512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-16]
OMIM:620699	Maple syrup urine disease, type II		HP:0011463	PMID:9621512	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-16]
OMIM:620699	Maple syrup urine disease, type II		HP:0000007	PMID:9621512	PCS					I	ORCID:0000-0002-0736-9199[2024-06-16]
OMIM:620699	Maple syrup urine disease, type II		HP:0003623	PMID:9621512	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-16]
OMIM:608115	Ovarian hyperstimulation syndrome		HP:0001541	OMIM:608115	IEA					P	HPO:iea[2009-02-17]
OMIM:608115	Ovarian hyperstimulation syndrome		HP:0000119	OMIM:608115	IEA					P	HPO:iea[2009-02-17]
OMIM:608115	Ovarian hyperstimulation syndrome		HP:0002018	OMIM:608115	IEA					P	HPO:iea[2009-02-17]
OMIM:608115	Ovarian hyperstimulation syndrome		HP:0000006	OMIM:608115	IEA					I	HPO:iea[2009-02-17]
OMIM:608115	Ovarian hyperstimulation syndrome		HP:0002027	OMIM:608115	IEA					P	HPO:iea[2009-02-17]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0001265	PMID:15021985	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0003477	PMID:15021985	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0003444	PMID:15021985	PCS					P	HPO:probinson[2012-04-19];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0003621	PMID:15021985	PCS					C	HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0002650	PMID:15021985	PCS		3/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0003387	PMID:15021985	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0001761	PMID:15021985	PCS		14/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0003693	PMID:15021985	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0001284	PMID:15021985	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0002460	PMID:15021985	PCS					P	HPO:probinson[2012-07-16];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0011462	PMID:15021985	PCS					C	HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0007078	PMID:15021985	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0002936	PMID:15021985	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608673	Charcot-Marie-Tooth disease, axonal, type 2L		HP:0000006	PMID:15021985	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0010804	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0002144	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000486	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0004322	PMID:30609410	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000089	PMID:30609410	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0003196	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001252	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000639	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000557	PMID:30609410	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001888	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000559	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001128	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0002553	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000252	PMID:30609410	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001344	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0011649	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0011968	OMIM:618460	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001263	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0005180	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0100259	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0034392	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000407	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000007	PMID:30609410	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000207	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000960	PMID:30609410	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001655	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000126	PMID:30609410	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001276	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0003577	PMID:30609410	PCS		2/2			C	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001476	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000580	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001508	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001903	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0002119	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000659	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0030084	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001320	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000076	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0002015	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0002650	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0031936	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0030048	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000073	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0011225	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0010535	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0011668	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000107	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000505	PMID:30609410	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001511	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0002007	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000347	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0000501	PMID:30609410	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-18]
OMIM:618460	Khan-Khan-Katsanis syndrome		HP:0001875	PMID:30609410	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300972	Immunodeficiency 47		HP:0001397	PMID:32216104;PMID:27231034	PCS		5/10			P	HPO:probinson[2021-10-02];HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001396	PMID:32216104	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0000540	PMID:27231034	PCS		3/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001250	PMID:27231034	PCS		6/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001252	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001395	PMID:32216104	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0003593	PMID:27231034	PCS		6/10			C	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0002240	PMID:29396028;PMID:32216104;PMID:27231034	PCS		11/14			P	HPO:probinson[2021-10-02];HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001394	PMID:27231034	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0032134	PMID:27231034	PCS		9/10			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0012301	PMID:29396028	IEA		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0031964	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0012347	PMID:32216104;PMID:27231034	PCS		13/13			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0002719	PMID:29396028;PMID:32216104	PCS		1/3			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001508	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0011463	PMID:27231034	PCS		1/10			C	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0002718	PMID:27231034	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0100702	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001747	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001522	PMID:32216104	PCS		2/2			C	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0002910	PMID:32216104;PMID:27231034	PCS		13/13			P	HPO:probinson[2021-10-02];HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001744	PMID:29396028;PMID:32216104;PMID:27231034	PCS		8/14			P	HPO:probinson[2021-10-02];HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0006579	PMID:27231034	PCS	HP:0003623	5/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0006579	PMID:32216104	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0003623	PMID:27231034	PCS		3/10			C	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0000973	PMID:29396028;PMID:32216104	PCS		3/3			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0002850	PMID:27231034	PCS		5/8			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0031956	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0004313	PMID:32216104;PMID:27231034	PCS		11/13			P	HPO:probinson[2021-10-02];HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001882	PMID:27231034	PCS		6/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0003124	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001382	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001263	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0003460	PMID:29396028;PMID:27231034	PCS		5/9			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0011967	PMID:32216104;PMID:27231034	PCS		12/12			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0012852	PMID:27231034	PCS		1/8			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0005180	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0012358	PMID:32216104;PMID:27231034	PCS		11/13			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001419	PMID:27231034	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0000407	PMID:27231034	PCS		3/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001738	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0032132	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0000601	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0000348	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001873	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0001897	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:300972	Immunodeficiency 47		HP:0002028	PMID:29396028	PCS		1/1			P	HPO:probinson[2021-10-02]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0001650	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0007879	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0008209	OMIM:176690	TAS					P	HPO:skoehler[2017-07-13]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0004322	OMIM:176690	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0001054	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000041	OMIM:176690	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0003193	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000819	OMIM:176690	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0100785	OMIM:176690	IEA					P	HPO:skoehler[2018-10-08]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000518	OMIM:176690	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0040079	OMIM:176690	TAS					P	HPO:skoehler[2014-11-26]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0001647	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0001367	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0001620	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0001249	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000572	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0002013	OMIM:176690	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0005101	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0005320	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0004791	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0011840	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0001518	OMIM:176690	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000407	OMIM:176690	TAS					P	HPO:skoehler[2012-11-21]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000668	OMIM:176690	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000007	OMIM:176690	TAS					I	HPO:skoehler[2012-10-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000823	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0004429	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000047	OMIM:176690	TAS					P	HPO:probinson[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0002943	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0000006	OMIM:176690	IEA					I	HPO:iea[2009-02-17]
OMIM:176690	Progeroid short stature with pigmented nevi		HP:0002721	OMIM:176690	IEA					P	HPO:iea[2009-02-17]
DECIPHER:38	Pelizaeus-Merzbacher disease		HP:0000639	DECIPHER:38	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:38	Pelizaeus-Merzbacher disease		HP:0001252	DECIPHER:38	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:38	Pelizaeus-Merzbacher disease		HP:0011400	DECIPHER:38	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:38	Pelizaeus-Merzbacher disease		HP:0002415	DECIPHER:38	IEA					P	HPO:skoehler[2013-05-29]
OMIM:144150	Hyperkeratosis lenticularis perstans		HP:0007570	OMIM:144150	IEA					P	HPO:iea[2009-02-17]
OMIM:144150	Hyperkeratosis lenticularis perstans		HP:0003581	OMIM:144150	IEA					C	HPO:iea[2009-02-17]
OMIM:144150	Hyperkeratosis lenticularis perstans		HP:0000006	OMIM:144150	IEA					I	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000286	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000582	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0003577	PMID:15821734	PCS		77/77			C	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0000365	PMID:15821734	PCS		8/77			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0000463	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0005235	PMID:15821734	PCS		2/77			P	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0000581	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0012745	PMID:15821734	PCS		56/77			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0011611	PMID:15821734	PCS	HP:0003577	1/77			P	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0010446	PMID:15821734	PCS	HP:0003577	1/77			P	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0001629	PMID:15821734	PCS		2/77			P	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0011662	PMID:15821734	PCS		1/77			P	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0012471	OMIM:164280	TAS					P	HPO:skoehler[2014-11-26]
OMIM:164280	Feingold syndrome 1		HP:0001746	OMIM:164280	TAS	HP:0003577				P	HPO:skoehler[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000437	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001328	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001748	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001605	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001747	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000218	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001643	PMID:15821734	PCS		9/77			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0001249	OMIM:164280	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164280	Feingold syndrome 1		HP:0000358	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000237	OMIM:164280	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0002575	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000252	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001561	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000431	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000232	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0002032	OMIM:164280	IEA	HP:0003577	25/77			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0004692	PMID:15821734	PCS		58/77			P	HPO:probinson[2013-04-07];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0004691	PMID:15821734	PCS		57/77			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0045025	OMIM:164280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:164280	Feingold syndrome 1		HP:0005819	PMID:15821734	PCS		77/77			P	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0001734	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001558	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0009778	PMID:15821734	PCS		13/77			P	HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0000006	PMID:15821734	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0002247	OMIM:164280	IEA		24/77			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0000369	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000347	PMID:15821734	PCS		25/77			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:164280	Feingold syndrome 1		HP:0000325	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000324	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0000269	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0001831	OMIM:164280	IEA					P	HPO:iea[2009-02-17]
OMIM:164280	Feingold syndrome 1		HP:0002589	PMID:15821734	PCS	HP:0003577	42/77			P	HPO:probinson[2022-10-19]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0004754	PMID:12522251;PMID:19632626	PCS		18/22			P	HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0003621	PMID:19632626	PCS		1/6			C	HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0003596	PMID:19632626	PCS		1/6			C	HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0001727	OMIM:607554;PMID:19632626	PCS		11/16			P	HPO:probinson[2012-04-10];HPO:probinson[2022-07-10];HPO:iea[2009-02-17]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0011462	PMID:12522251;PMID:19632626	PCS		5/7			C	HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0005110	PMID:12522251	PCS					P	HPO:probinson[2012-04-10];HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0005184	PMID:12522251	PCS		9/16			P	HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0001279	PMID:12522251	PCS		2/16			P	HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0004757	PMID:19632626	PCS		4/6			P	HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0000006	PMID:12522251	PCS					I	HPO:probinson[2012-04-10];HPO:probinson[2022-07-10]
OMIM:607554	Atrial fibrillation, familial, 3		HP:0001645	PMID:12522251	PCS		0/16			P	HPO:probinson[2022-07-10]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0003510	PMID:13679528	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0006527	PMID:13679528	PCS	HP:0011463	1/1			P	HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0002098	PMID:13679528	IEA		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0001508	PMID:13679528	PCS	HP:0003593	1/1			P	HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0011220	PMID:13679528	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0011120	PMID:13679528	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0000007	PMID:13679528	PCS					I	HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0000824	PMID:13679528	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-12-02]
OMIM:245590	Growth hormone insensitivity with immune dysregulation 1, autosomal recessive		HP:0001620	PMID:13679528	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:109050	Auralcephalosyndactyly		HP:0001363	OMIM:109050	IEA					P	HPO:iea[2009-02-17]
OMIM:109050	Auralcephalosyndactyly		HP:0000365	OMIM:109050	IEA					P	HPO:iea[2009-02-17]
OMIM:109050	Auralcephalosyndactyly		HP:0002000	OMIM:109050	IEA					P	HPO:iea[2009-02-17]
OMIM:109050	Auralcephalosyndactyly		HP:0004692	OMIM:109050	IEA					P	HPO:iea[2009-02-17]
OMIM:109050	Auralcephalosyndactyly		HP:0030680	OMIM:109050	IEA					P	HPO:iea[2009-02-17]
OMIM:109050	Auralcephalosyndactyly		HP:0000006	OMIM:109050	IEA					I	HPO:iea[2009-02-17]
OMIM:616459	Al-Raqad syndrome		HP:0003577	PMID:25712129	PCS		6/6			C	HPO:probinson[2023-03-12];HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0000252	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-08-02]
OMIM:616459	Al-Raqad syndrome		HP:0001344	PMID:25712129	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0002540	PMID:25712129	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0000750	PMID:25712129	PCS		3/3			P	HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0001156	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:616459	Al-Raqad syndrome		HP:0031936	PMID:25712129	PCS		3/3			P	HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0001382	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:616459	Al-Raqad syndrome		HP:0001250	PMID:25712129	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0000490	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:616459	Al-Raqad syndrome		HP:0000160	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:616459	Al-Raqad syndrome		HP:0002066	PMID:25712129	PCS		1/3			P	HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0001263	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0001010	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:616459	Al-Raqad syndrome		HP:0001252	PMID:25712129	PCS	HP:0003577	3/3			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0003196	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:616459	Al-Raqad syndrome		HP:0012368	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0012450	PMID:25712129	PCS		3/3			P	HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0000007	PMID:25712129	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0000219	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0025336	PMID:25712129	PCS		3/3			P	HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0001852	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:616459	Al-Raqad syndrome		HP:0001631	PMID:25712129	PCS		3/3			P	HPO:probinson[2023-03-12]
OMIM:616459	Al-Raqad syndrome		HP:0000369	PMID:25712129	PCS		3/3			P	HPO:skoehler[2015-12-30]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000365	PMID:26637982	PCS		5/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000486	PMID:26637982	PCS		8/12			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001057	PMID:26637982	PCS		5/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001332	PMID:26637982	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001250	PMID:26637982	PCS		1/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001251	PMID:26637982	PCS		2/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002141	PMID:26637982	PCS		4/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002020	PMID:26637982	PCS		4/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001290	PMID:26637982	PCS		9/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0011410	PMID:26637982	PCS		6/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0040016	PMID:26637982	PCS		9/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000639	PMID:26637982	PCS		2/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0011220	PMID:26637982	PCS		5/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000437	PMID:26637982	PCS					P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000316	PMID:26637982	PCS		4/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0008897	PMID:26637982	PCS		8/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002019	PMID:26637982	PCS		6/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001007	PMID:26637982	PCS		3/12			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001249	PMID:26637982	PCS		10/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0005469	PMID:26637982	PCS		1/6			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000494	PMID:26637982	PCS		7/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001385	PMID:26637982	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000252	PMID:26637982	PCS		7/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001264	PMID:26637982	PCS		3/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0006979	PMID:26637982	PCS		3/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000496	PMID:26637982	PCS		3/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002079	PMID:26637982	PCS		6/7			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0004696	PMID:26637982	PCS		3/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001382	PMID:26637982	PCS		6/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000490	PMID:26637982	PCS		7/14			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001263	PMID:26637982	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0011927	PMID:26637982	PCS		3/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002194	PMID:26637982	PCS		10/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001419	PMID:26637982	PCS					I	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000729	PMID:26637982	PCS		7/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0009894	PMID:26637982	PCS		5/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000767	PMID:26637982	PCS		2/7			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000964	PMID:26637982	PCS		3/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002705	PMID:26637982	PCS		8/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000400	PMID:26637982	PCS					P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000520	PMID:26637982	PCS					P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000960	PMID:26637982	PCS		3/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001257	PMID:26637982	PCS		4/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000369	PMID:26637982	PCS		9/12			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001337	PMID:26637982	PCS		1/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0003577	PMID:26637982	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000343	PMID:26637982	PCS		7/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000463	PMID:26637982	PCS		8/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001272	PMID:26637982	PCS		4/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0008070	PMID:26637982	PCS		1/7			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0008472	PMID:26637982	PCS		10/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000938	PMID:26637982	PCS		2/4			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000739	PMID:26637982	PCS		4/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000414	PMID:26637982	PCS					P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000579	PMID:26637982	PCS		1/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000219	PMID:26637982	PCS		5/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002119	PMID:26637982	PCS		5/8		HP:0012825	P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000455	PMID:26637982	PCS					P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000411	PMID:26637982	PCS		11/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000336	PMID:26637982	PCS		7/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001320	PMID:26637982	PCS		3/6			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000750	PMID:26637982	PCS		8/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002650	PMID:26637982	PCS		4/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001321	PMID:26637982	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001288	PMID:26637982	PCS		4/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000276	PMID:26637982	PCS		7/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000391	PMID:26637982	PCS					P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000470	PMID:26637982	PCS		5/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0011822	PMID:26637982	PCS					P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0100797	PMID:26637982	PCS		4/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0002808	PMID:26637982	PCS		4/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000308	PMID:26637982	PCS		4/9			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0007375	PMID:26637982	PCS		1/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0200136	PMID:26637982	PCS		5/6			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000307	PMID:26637982	PCS		7/11			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000389	PMID:26637982	PCS		6/10			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001511	PMID:26637982	PCS		4/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000664	PMID:26637982	PCS		4/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0007018	PMID:26637982	PCS		2/8			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0000545	PMID:26637982	PCS		4/7			P	HPO:probinson[2017-06-17]
OMIM:300966	Intellectual developmental disorder, X-linked syndromic 33		HP:0001315	PMID:26637982	PCS		3/5			P	HPO:probinson[2017-06-17]
OMIM:609579	Familial scaphocephaly syndrome, Mcgillivray type		HP:0000268	OMIM:609579	IEA					P	HPO:skoehler[2015-01-21]
OMIM:609579	Familial scaphocephaly syndrome, Mcgillivray type		HP:0001249	OMIM:609579	IEA					P	HPO:skoehler[2015-01-21]
OMIM:156232	Mesomelic dysplasia, Kantaputra type		HP:0003027	OMIM:156232	IEA					P	HPO:iea[2009-02-17]
OMIM:156232	Mesomelic dysplasia, Kantaputra type		HP:0008368	OMIM:156232	TAS					P	HPO:probinson[2009-02-17]
OMIM:156232	Mesomelic dysplasia, Kantaputra type		HP:0002986	OMIM:156232	IEA					P	HPO:iea[2009-02-17]
OMIM:156232	Mesomelic dysplasia, Kantaputra type		HP:0009702	OMIM:156232	TAS					P	HPO:probinson[2009-02-17]
OMIM:156232	Mesomelic dysplasia, Kantaputra type		HP:0000006	OMIM:156232	IEA					I	HPO:iea[2009-02-17]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0003577	OMIM:617021	TAS					C	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001410	PMID:26537577	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0030674	PMID:26537577	PCS		1/1			C	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001250	PMID:26537577	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001790	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0003073	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0012132	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001629	PMID:26537577	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001903	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001924	OMIM:617021	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001643	PMID:26537577	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001942	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0003128	PMID:26537577	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001562	PMID:26537577	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0025671	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0002353	OMIM:617021	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001541	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0000790	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0002151	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0011706	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0002092	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0002093	OMIM:617021	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001518	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0000822	OMIM:617021	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0000007	PMID:26537577	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001978	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0005518	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001511	PMID:26537577	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0002623	PMID:26537577	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:617021	Hydrops, lactic acidosis, and sideroblastic anemia		HP:0001873	OMIM:617021	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618312	Diamond-Blackfan anemia 19		HP:0012133	PMID:28280134	PCS		2/2			P	HPO:probinson[2020-05-08]
OMIM:618312	Diamond-Blackfan anemia 19		HP:0033074	PMID:28280134	PCS	HP:0003593	1/2			P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:618312	Diamond-Blackfan anemia 19		HP:0001903	PMID:28280134	PCS	HP:0003593	2/2			P	HPO:probinson[2020-05-08]
OMIM:618312	Diamond-Blackfan anemia 19		HP:0000006	PMID:28280134	PCS					I	HPO:probinson[2020-05-08];HPO:probinson[2020-05-08]
OMIM:140450	Heart-hand syndrome, Spanish type		HP:0001156	OMIM:140450	IEA					P	HPO:iea[2009-02-17]
OMIM:140450	Heart-hand syndrome, Spanish type		HP:0011704	OMIM:140450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:140450	Heart-hand syndrome, Spanish type		HP:0009464	OMIM:140450	IEA					P	HPO:iea[2009-02-17]
OMIM:140450	Heart-hand syndrome, Spanish type		HP:0005819	OMIM:140450	TAS					P	HPO:skoehler[2009-02-17]
OMIM:140450	Heart-hand syndrome, Spanish type		HP:0001626	OMIM:140450	IEA					P	HPO:iea[2009-02-17]
OMIM:140450	Heart-hand syndrome, Spanish type		HP:0000006	OMIM:140450	IEA					I	HPO:iea[2009-02-17]
OMIM:137800	Glioma susceptibility 1		HP:0001442	OMIM:137800	TAS					I	HPO:skoehler[2013-01-21]
OMIM:137800	Glioma susceptibility 1		HP:0009592	OMIM:137800	TAS					P	HPO:skoehler[2013-01-22]
OMIM:137800	Glioma susceptibility 1		HP:0012174	OMIM:137800	TAS					P	HPO:probinson[2009-02-17]
OMIM:137800	Glioma susceptibility 1		HP:0002888	OMIM:137800	TAS					P	HPO:skoehler[2013-01-22]
OMIM:137800	Glioma susceptibility 1		HP:0000006	OMIM:137800	TAS					I	HPO:skoehler[2013-01-21]
OMIM:241090	Hypogonadism, primary, and partial alopecia		HP:0001596	OMIM:241090	TAS					P	HPO:skoehler[2010-06-20]
OMIM:241090	Hypogonadism, primary, and partial alopecia		HP:0000815	OMIM:241090	TAS					P	HPO:probinson[2009-02-17]
OMIM:241090	Hypogonadism, primary, and partial alopecia		HP:0000007	OMIM:241090	TAS					I	HPO:skoehler[2009-02-17]
OMIM:241090	Hypogonadism, primary, and partial alopecia		HP:0010464	OMIM:241090	TAS					P	HPO:probinson[2013-08-11]
OMIM:615636	Joubert syndrome 21		HP:0003577	OMIM:615636	TAS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0002089	PMID:24360808	PCS		4/19			P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0000486	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0002365	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0001591	PMID:24360808	PCS		4/19			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0001250	PMID:24360808	PCS		1/18			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0001252	OMIM:615636	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615636	Joubert syndrome 21		HP:0002085	OMIM:615636	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0001251	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0002084	PMID:24360808	PCS		1/18			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0011933	PMID:24360808	PCS		0/10			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0000639	PMID:24360808	PCS		6/18			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0004719	OMIM:615636	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0000657	PMID:24360808	PCS		4/18			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0000316	PMID:24360808	PCS		4/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0002878	PMID:24360808	PCS		2/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0000773	PMID:24360808	PCS		4/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0001249	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0001744	PMID:24360808	PCS		1/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0002015	PMID:24360808	PCS		1/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0002079	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0001263	PMID:24360808	PCS		19/19			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0002094	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0034302	PMID:24360808	PCS		1/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0011109	PMID:24360808	PCS		2/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0007291	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0000528	OMIM:615636	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0000407	PMID:24360808	PCS		2/19			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0000508	PMID:24360808	PCS		15/18			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0000107	OMIM:615636	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615636	Joubert syndrome 21		HP:0000007	PMID:24360808	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2023-03-28]
OMIM:615636	Joubert syndrome 21		HP:0000648	PMID:24360808	PCS		1/19			P	HPO:probinson[2023-06-04]
OMIM:615636	Joubert syndrome 21		HP:0000488	OMIM:615636	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0009932	OMIM:615636	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:615636	Joubert syndrome 21		HP:0002104	OMIM:615636	TAS					P	HPO:skoehler[2014-03-24]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003323	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003236	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003621	PMID:29361167	PCS		1/1			C	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003200	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0001288	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0011924	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003551	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0011923	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0000007	PMID:29361167	PCS					I	HPO:probinson[2020-12-02];HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0008347	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0008314	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02];HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003688	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003326	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:619024	Combined oxidative phosphorylation deficiency 49		HP:0003546	PMID:29361167	PCS		1/1			P	HPO:probinson[2020-12-02]
OMIM:614500	Cone-Rod dystrophy 16		HP:0007737	PMID:22177090	IEA		2/6			P	HPO:probinson[2017-05-30]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000662	PMID:22177090	PCS					P	HPO:probinson[2017-05-30]
OMIM:614500	Cone-Rod dystrophy 16		HP:0025147	PMID:22177090	PCS					P	HPO:probinson[2017-05-30]
OMIM:614500	Cone-Rod dystrophy 16		HP:0100259	PMID:22177090	PCS		2/6			P	HPO:skoehler[2012-11-18]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000529	PMID:22177090	PCS					P	HPO:probinson[2017-05-30]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000518	OMIM:614500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000613	PMID:22177090	PCS					P	HPO:probinson[2017-05-30]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000007	PMID:22177090	PCS					I	HPO:skoehler[2012-10-17]
OMIM:614500	Cone-Rod dystrophy 16		HP:0007663	PMID:22177090	PCS					P	HPO:probinson[2017-05-30]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000548	PMID:22177090	PCS					P	HPO:skoehler[2015-01-19]
OMIM:614500	Cone-Rod dystrophy 16		HP:0007401	PMID:22177090	PCS					P	HPO:skoehler[2015-07-26]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000543	PMID:22177090	PCS		3/6			P	HPO:skoehler[2012-11-18]
OMIM:614500	Cone-Rod dystrophy 16		HP:0000510	PMID:22177090	PCS					P	HPO:skoehler[2015-01-19]
OMIM:614500	Cone-Rod dystrophy 16		HP:0007843	PMID:22177090	PCS		4/6			P	HPO:probinson[2017-05-30]
OMIM:145500	Hypertension, essential		HP:0005117	OMIM:145500	IEA					P	HPO:iea[2009-02-17]
OMIM:145500	Hypertension, essential		HP:0004972	OMIM:145500	IEA					P	HPO:iea[2009-02-17]
OMIM:145500	Hypertension, essential		HP:0004421	OMIM:145500	IEA					P	HPO:iea[2009-02-17]
OMIM:145500	Hypertension, essential		HP:0001426	OMIM:145500	IEA					I	HPO:iea[2009-02-17]
OMIM:614266	Barrett esophagus		HP:0001442	OMIM:614266	TAS					I	HPO:probinson[2013-08-10]
OMIM:614266	Barrett esophagus		HP:0004791	PMID:14791960	PCS		HP:0040281			P	HPO:lccarmody[2018-10-04];HP:probinson[2019-01-03]
OMIM:614266	Barrett esophagus		HP:0002020	PMID:14791960	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:614266	Barrett esophagus		HP:0100580	OMIM:614266	TAS					P	HPO:probinson[2013-01-09]
OMIM:614266	Barrett esophagus		HP:0011459	OMIM:614266	TAS					P	HPO:probinson[2013-08-10]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0003510	PMID:12000367	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0000343	PMID:12000367	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0002750	PMID:12000367	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0000160	PMID:12000367	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0001263	PMID:12000367	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0001252	PMID:12000367	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0000407	PMID:12000367	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0000316	OMIM:613509	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0000337	OMIM:613509	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0006872	OMIM:613509	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0008897	OMIM:613509	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0002714	OMIM:613509	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0002007	OMIM:613509	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0003745	PMID:12000367	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0000268	PMID:12000367	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613509	Chromosome 4q21 deletion syndrome		HP:0000322	OMIM:613509	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001265	PMID:33417887	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0000252	PMID:33417887	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0000750	PMID:33417887	PCS		4/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0006858	PMID:33417887	PCS		1/2			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0002188	PMID:33417887	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0031936	PMID:33417887	PCS		3/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0003487	PMID:33417887	PCS		4/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001272	PMID:33417887	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001250	PMID:33417887	PCS		3/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001260	PMID:33417887	PCS		5/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001263	PMID:33417887	PCS		5/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001251	PMID:33417887	PCS		3/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0002064	PMID:33417887	PCS		4/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0003593	PMID:33417887	PCS		4/6			C	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0031058	PMID:33417887	PCS		4/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0011463	PMID:33417887	PCS		2/6			C	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0007099	PMID:33417887	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0002359	PMID:33417887	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001257	PMID:33417887	PCS		4/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0006886	PMID:33417887	PCS		1/2			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0000006	PMID:33417887	PCS					I	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001249	PMID:33417887	PCS		5/6			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0007108	PMID:33417887	PCS		5/6			P	HPO:probinson[2022-04-19]
OMIM:619742	Charcot-Marie-Tooth disease, demyelinating, type 1I		HP:0001347	PMID:33417887	PCS		3/6			P	HPO:probinson[2022-04-19]
OMIM:616471	Bethlem myopathy 2		HP:0003236	PMID:24334769	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0002650	PMID:24334604	PCS		0/1			P	HPO:skoehler[2015-09-17];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0031936	OMIM:616471	TAS					P	HPO:skoehler[2018-10-08]
OMIM:616471	Bethlem myopathy 2		HP:0001371	PMID:24334604	PCS		1/1			P	HPO:skoehler[2015-09-17];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0003198	PMID:24334604	PCS					P	HPO:skoehler[2015-09-17];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0020152	PMID:24334604	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0001252	PMID:24334604	PCS	HP:0003593	1/1			P	HPO:skoehler[2015-09-17];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0003691	PMID:24334769	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0001075	PMID:24334769	PCS		3/5			P	HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0001290	PMID:24334769	PCS	HP:0003593	1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0001270	PMID:24334604	PCS		1/1			P	HPO:skoehler[2015-09-17];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0002808	PMID:24334604	PCS		1/1			P	HPO:skoehler[2015-09-17];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0002827	PMID:24334769	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0009046	OMIM:616471	TAS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0025403	PMID:24334604	PCS	HP:0011463	1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0001324	PMID:24334769	PCS	HP:0011463	5/5			P	HPO:skoehler[2015-09-17];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0003701	PMID:24334769	PCS		5/5			P	HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0000006	PMID:24334604	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:616471	Bethlem myopathy 2		HP:0003557	PMID:24334604	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:141000	Hemangioma-Thrombocytopenia syndrome		HP:0001937	OMIM:141000	IEA					P	HPO:iea[2009-02-17]
OMIM:141000	Hemangioma-Thrombocytopenia syndrome		HP:0002153	OMIM:141000	IEA					P	HPO:iea[2009-02-17]
OMIM:141000	Hemangioma-Thrombocytopenia syndrome		HP:0004308	OMIM:141000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:141000	Hemangioma-Thrombocytopenia syndrome		HP:0001873	OMIM:141000	IEA					P	HPO:iea[2009-02-17]
OMIM:141000	Hemangioma-Thrombocytopenia syndrome		HP:0000006	OMIM:141000	IEA					I	HPO:iea[2009-02-17]
OMIM:141000	Hemangioma-Thrombocytopenia syndrome		HP:0001028	OMIM:141000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272300	SULFOCYSTEINURIA		HP:0002069	PMID:15952210	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0001276	OMIM:272300	IEA					P	HPO:iea[2009-02-17]
OMIM:272300	Sulfite oxidase deficiency		HP:0008947	OMIM:272300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:272300	SULFOCYSTEINURIA		HP:0000341	PMID:15952210	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0002301	OMIM:272300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272300	SULFOCYSTEINURIA		HP:0003236	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0000684	OMIM:272300	TAS					P	HPO:probinson[2013-12-18]
OMIM:272300	Sulfite oxidase deficiency		HP:0001251	OMIM:272300	IEA					P	HPO:iea[2009-02-17]
OMIM:272300	Sulfite oxidase deficiency		HP:0001290	OMIM:272300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0010841	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0100704	PMID:15952210	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0000713	PMID:31127934	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0001522	OMIM:272300	TAS					C	HPO:skoehler[2009-02-17]
OMIM:272300	Sulfite oxidase deficiency		HP:0007325	OMIM:272300	IEA					P	HPO:iea[2009-02-17]
OMIM:272300	SULFOCYSTEINURIA		HP:0001942	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0003623	PMID:15952210;PMID:31127934	PCS		2/2			C	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0008936	PMID:15952210	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0002213	OMIM:272300	IEA					P	HPO:iea[2009-02-17]
OMIM:272300	Sulfite oxidase deficiency		HP:0003643	PMID:15952210	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0000252	PMID:15952210;PMID:31127934	PCS		2/2			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0002059	PMID:15952210	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0001344	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0001266	OMIM:272300	IEA					P	HPO:iea[2009-02-17]
OMIM:272300	SULFOCYSTEINURIA		HP:0001321	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0000490	PMID:15952210	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0002572	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0001263	PMID:15952210	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0011942	OMIM:272300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272300	Sulfite oxidase deficiency		HP:0001083	OMIM:272300	IEA					P	HPO:iea[2009-02-17]
OMIM:272300	SULFOCYSTEINURIA		HP:0100660	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0032350	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	SULFOCYSTEINURIA		HP:0030890	PMID:31127934	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0000007	PMID:15952210	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0000964	OMIM:272300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272300	SULFOCYSTEINURIA		HP:0000400	PMID:15952210	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:272300	Sulfite oxidase deficiency		HP:0003359	OMIM:272300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0005543	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0000707	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0100724	OMIM:176860	IEA					P	HPO:skoehler[2015-01-27]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0002638	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0002625	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0001038	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0000006	OMIM:176860	IEA					I	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0000478	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0002204	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:176860	Thrombophilia, hereditary, due to protein C deficiency, autosomaldominant		HP:0005305	OMIM:176860	IEA					P	HPO:iea[2009-02-17]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0001342	PMID:20484936	PCS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0005521	PMID:20484936	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0004420	OMIM:614514	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0001250	PMID:20484936	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0001903	PMID:20484936	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0000979	PMID:20484936	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0000618	OMIM:614514	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0100724	PMID:20484936	PCS		1/1			P	HPO:skoehler[2015-01-27]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0002638	OMIM:614514	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0000007	PMID:20484936	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0004855	PMID:20484936	PCS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0005305	OMIM:614514	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0003623	PMID:20484936	PCS		1/1			C	HPO:probinson[2023-06-04]
OMIM:614514	Thrombophilia due to protein S deficiency, autosomal recessive		HP:0002204	OMIM:614514	TAS					P	HPO:skoehler[2012-10-17]
OMIM:276600	Tyrosine transaminase deficiency		HP:0003231	OMIM:276600	IEA					P	HPO:iea[2009-02-17]
OMIM:276600	Tyrosine transaminase deficiency		HP:0003161	OMIM:276600	IEA					P	HPO:iea[2009-02-17]
OMIM:276600	Tyrosine transaminase deficiency		HP:0000007	OMIM:276600	IEA					I	HPO:iea[2009-02-17]
OMIM:276600	Tyrosine transaminase deficiency		HP:6000479	PMID:20301688	PCS					P	HPO:probinson[2024-04-03]
OMIM:276600	Tyrosine transaminase deficiency		HP:0001510	OMIM:276600	IEA					P	HPO:iea[2009-02-17]
OMIM:276600	Tyrosine transaminase deficiency		HP:0001249	OMIM:276600	IEA					P	HPO:iea[2009-02-17]
OMIM:276600	Tyrosine transaminase deficiency		HP:0000951	OMIM:276600	IEA					P	HPO:iea[2009-02-17]
OMIM:276600	Tyrosine transaminase deficiency		HP:0007812	OMIM:276600	IEA					P	HPO:iea[2009-02-17]
OMIM:605419	Schizophrenia 10		HP:0005324	OMIM:605419	IEA					P	HPO:iea[2009-02-17]
OMIM:605419	Schizophrenia 10		HP:0000298	OMIM:605419	IEA					P	HPO:iea[2009-02-17]
OMIM:605419	Schizophrenia 10		HP:0100753	OMIM:605419	IEA					P	HPO:skoehler[2015-01-19]
OMIM:605419	Schizophrenia 10		HP:0000738	OMIM:605419	IEA					P	HPO:iea[2009-02-17]
OMIM:605419	Schizophrenia 10		HP:0000725	OMIM:605419	IEA					P	HPO:iea[2009-02-17]
OMIM:605419	Schizophrenia 10		HP:0000746	OMIM:605419	IEA					P	HPO:iea[2009-02-17]
OMIM:605419	Schizophrenia 10		HP:0000006	OMIM:605419	IEA					I	HPO:iea[2009-02-17]
OMIM:612165	Retinitis pigmentosa 29		HP:0000618	OMIM:612165	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612165	Retinitis pigmentosa 29		HP:0000007	OMIM:612165	TAS					I	HPO:skoehler[2014-01-28]
OMIM:612165	Retinitis pigmentosa 29		HP:0000510	OMIM:612165	TAS					P	HPO:skoehler[2014-01-28]
OMIM:612165	Retinitis pigmentosa 29		HP:0007843	OMIM:612165	TAS					P	HPO:skoehler[2014-01-28]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0003301	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0003521	OMIM:609223	TAS					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0002650	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0006429	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0002970	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0003370	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0003184	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0000926	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0002938	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0000007	OMIM:609223	IEA					I	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0000768	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0002857	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0002945	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0002942	OMIM:609223	IEA					P	HPO:iea[2009-02-17]
OMIM:609223	Spondyloepiphyseal dysplasia tarda, autosomal recessive, leroy-sprangertype		HP:0002655	OMIM:609223	TAS		20/20			P	HPO:iea[2009-02-17]
OMIM:620869	Immunodeficiency 122		HP:0410378	PMID:37030525;PMID:38099988	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0005359	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0410377	PMID:37030525;PMID:38099988	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0002783	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0001596	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0003212	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0002240	PMID:37030525	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0003593	PMID:37030525;PMID:38099988	PCS		2/2			C	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0001270	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0000958	PMID:37030525	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0006297	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0002718	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0002716	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0001744	PMID:37030525;PMID:38099988	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0040218	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0004315	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0005403	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0001880	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0011968	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0002110	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0004430	PMID:37030525;PMID:38099988	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0410243	PMID:37030525;PMID:38099988	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0001263	PMID:37030525;PMID:38099988	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0031430	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0032126	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0010975	PMID:37030525	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0000407	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0500093	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0001999	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0001019	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0000007	PMID:37030525	PCS					I	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0004429	PMID:38099988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0002788	PMID:37030525;PMID:38099988	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0002007	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620869	Immunodeficiency 122		HP:0008404	PMID:37030525;PMID:38099988	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0005667	OMIM:600561	TAS					P	HPO:probinson[2012-06-10]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0003467	OMIM:600561	TAS					P	HPO:probinson[2012-06-10]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0002750	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0004322	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0001283	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0001382	OMIM:600561	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0002273	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0003690	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0011448	OMIM:600561	TAS					P	HPO:probinson[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0003090	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0009130	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0002938	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0001308	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0002878	OMIM:600561	TAS					P	HPO:probinson[2014-05-29]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0008489	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0001269	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0000006	OMIM:600561	IEA					I	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0001348	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0002655	OMIM:600561	TAS					P	HPO:probinson[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0003304	OMIM:600561	TAS					P	HPO:probinson[2009-02-17]
OMIM:600561	Spondyloepiphyseal dysplasia with atlantoaxial instability		HP:0003414	OMIM:600561	IEA					P	HPO:iea[2009-02-17]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002421	OMIM:614299	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001254	PMID:21944046	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001250	PMID:21944046	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0003593	PMID:21944046	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002240	PMID:21944046	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001251	OMIM:614299	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001290	OMIM:614299	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0008972	OMIM:614299	TAS					P	HPO:skoehler[2013-05-29]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0000975	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002878	OMIM:614299	TAS					P	HPO:skoehler[2014-06-24]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0008314	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001324	OMIM:614299	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001522	PMID:21944046	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002415	OMIM:614299	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0003128	PMID:21944046	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001644	PMID:21944046	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002013	OMIM:614299	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002376	OMIM:614299	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002098	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0011924	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002154	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001263	PMID:21944046	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002093	OMIM:614299	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002071	OMIM:614299	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0011923	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:6000829	PMID:24334290	PCS					P	HPO:probinson[2024-08-03]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0500230	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002928	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001639	OMIM:614299	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0000007	PMID:21944046	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0000505	OMIM:614299	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0000648	OMIM:614299	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0200134	PMID:21944046	PCS		1/1			P	HPO:skoehler[2013-06-11];HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0002789	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001257	OMIM:614299	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614299	Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia		HP:0001336	OMIM:614299	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617948	Elliptocytosis-3		HP:0004445	PMID:9163587	PCS		3/3			P	HPO:probinson[2020-03-28]
OMIM:617948	Elliptocytosis-3		HP:0025066	PMID:9163587	PCS		1/3			P	HPO:probinson[2020-03-28]
OMIM:617948	Elliptocytosis-3		HP:0001046	PMID:3580577	PCS					P	HPO:probinson[2020-03-28]
OMIM:617948	Elliptocytosis-3		HP:0004870	PMID:9163587	PCS					P	HPO:probinson[2020-03-28];HPO:probinson[2020-03-28]
OMIM:617948	Elliptocytosis-3		HP:0004839	PMID:9075575	PCS					P	HPO:probinson[2020-03-28]
OMIM:617948	Elliptocytosis-3		HP:0000006	PMID:9163587	PCS					I	HPO:probinson[2020-03-28];HPO:probinson[2020-03-28]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0002100	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001250	PMID:33833240;PMID:34909687	PCS		7/7			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001272	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0003593	PMID:33833240	PCS		1/2			C	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0002020	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001251	PMID:34909687	PCS		5/5			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0000939	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0011462	PMID:34909687	PCS		1/5			C	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0002539	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0007366	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001249	PMID:34909687	PCS		5/5			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0003623	PMID:33833240	PCS		1/2			C	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0002510	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001561	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0003621	PMID:34909687	PCS		4/5			C	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0002254	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001321	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0011968	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0025357	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001263	PMID:33833240	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0004395	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0010851	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0011097	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0000007	PMID:33833240	PCS					I	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0007018	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0000303	PMID:34909687	PCS		4/4			P	HPO:probinson[2022-08-20]
OMIM:619971	Neurodevelopmental disorder with epilepsy and brain atrophy		HP:0001336	PMID:34909687	PCS		5/5			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:617784	Fanconi anemia, complementation group W		HP:0000252	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0003577	OMIM:617784	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617784	Fanconi anemia, complementation group W		HP:0000089	OMIM:617784	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617784	Fanconi anemia, complementation group W		HP:0011800	OMIM:617784	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617784	Fanconi anemia, complementation group W		HP:0031689	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0002308	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0000007	PMID:28691929	PCS					I	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0002518	OMIM:617784	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617784	Fanconi anemia, complementation group W		HP:0000824	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0001748	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0009777	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0002119	OMIM:617784	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617784	Fanconi anemia, complementation group W		HP:0006433	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0001511	OMIM:617784	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617784	Fanconi anemia, complementation group W		HP:0001510	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0002863	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0002984	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:617784	Fanconi anemia, complementation group W		HP:0002247	PMID:28691929	PCS		1/1			P	HPO:probinson[2018-04-13]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000494	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000185	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0001263	OMIM:606851	IEA		20/20			P	HPO:skoehler[2019-04-18];HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0010554	OMIM:606851	TAS					P	HPO:probinson[2012-07-25]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0001838	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000508	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000239	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000316	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000767	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000007	OMIM:606851	IEA					I	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000048	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000047	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000465	OMIM:606851	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000028	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000248	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000325	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000347	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000358	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000369	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0000589	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0001249	OMIM:606851	TAS					P	HPO:skoehler[2015-01-21]
OMIM:606851	Cree impaired intellectual development syndrome		HP:0006712	OMIM:606851	IEA					P	HPO:iea[2009-02-17]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0001541	OMIM:174050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0003155	OMIM:174050	TAS		HP:0040283		HP:0012825	P	HPO:skoehler[2009-02-17]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0003573	OMIM:174050	IEA					P	HPO:iea[2009-02-17]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0003581	PMID:12577059	PCS		6/6			C	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-08]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0000107	OMIM:174050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0002094	OMIM:174050	IEA					P	HPO:skoehler[2019-09-07]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0003270	OMIM:174050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0003418	OMIM:174050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0004944	PMID:12577059	PCS		0/6			P	HPO:probinson[2024-03-08]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0000006	PMID:12577059	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:174050	Polycystic liver disease 1 with or without kidney cysts		HP:0006557	PMID:12577059	PCS		6/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-08]
OMIM:615193	Bleeding disorder, platelet-type, 15		HP:0011877	PMID:23434115	PCS		13/13			P	HPO:skoehler[2013-05-07];HP:probinson[2019-05-27]
OMIM:615193	Bleeding disorder, platelet-type, 15		HP:0031126	PMID:23434115	PCS		0/1			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:615193	Bleeding disorder, platelet-type, 15		HP:0000421	PMID:23434115	PCS		2/13			P	HPO:skoehler[2013-05-07];HP:probinson[2019-05-27]
OMIM:615193	Bleeding disorder, platelet-type, 15		HP:0001873	PMID:23434115	PCS		13/13			P	HPO:skoehler[2013-05-07];HP:probinson[2019-05-27]
OMIM:615193	Bleeding disorder, platelet-type, 15		HP:0000006	PMID:23434115	PCS					I	HPO:skoehler[2013-05-07];HP:probinson[2019-05-27]
OMIM:615193	Bleeding disorder, platelet-type, 15		HP:0004866	PMID:23434115	PCS		0/6			P	HP:probinson[2019-05-27];HPO:probinson[2024-03-15]
OMIM:615193	Bleeding disorder, platelet-type, 15		HP:0032438	PMID:23434115	PCS		13/13			P	HP:probinson[2019-05-27];HP:probinson[2019-05-27]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000252	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000340	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0002650	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0001371	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0005432	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0003065	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0002719	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000007	OMIM:251240	IEA					I	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000400	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000411	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000444	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000135	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:251240	Microcephaly with chemotactic defect and transient hypogammaglobulinemia		HP:0000347	OMIM:251240	IEA					P	HPO:iea[2009-02-17]
OMIM:107900	Arms, malformation of		HP:0003022	OMIM:107900	TAS					P	HPO:probinson[2013-04-07]
OMIM:107900	Arms, malformation of		HP:0000006	OMIM:107900	TAS					I	HPO:probinson[2009-02-17]
OMIM:107900	Arms, malformation of		HP:0002984	OMIM:107900	TAS					P	HPO:probinson[2013-04-07]
OMIM:107900	Arms, malformation of		HP:0002974	OMIM:107900	TAS					P	HPO:probinson[2013-04-07]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0004754	PMID:15368194	PCS		1/10			P	HPO:lccarmody[2018-06-29]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0003596	PMID:15368194	PCS		3/4			C	HPO:probinson[2022-07-10]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0003584	PMID:15368194	PCS		1/4			C	HPO:probinson[2022-07-10]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0005110	PMID:15368194	PCS		9/9			P	HPO:probinson[2013-02-26];HP:probinson[2018-07-14]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0001962	PMID:15368194	PCS		9/10			P	HPO:lccarmody[2018-06-29]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0004757	PMID:15368194	PCS		3/10			P	HPO:lccarmody[2018-06-29]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0006699	PMID:15368194	PCS		10/10			P	HPO:lccarmody[2018-06-29]
OMIM:611493	Atrial fibrillation, familial, 4		HP:0000006	PMID:15368194	PCS					I	HPO:probinson[2013-01-09]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000494	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0003049	OMIM:601680	TAS					P	HPO:probinson[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0006109	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000343	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000431	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0001762	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0002650	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0004322	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000160	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0005684	OMIM:601680	TAS					P	HPO:probinson[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0100490	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0001193	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0005272	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0001838	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0001848	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0002804	OMIM:601680	IEA					P	HPO:skoehler[2015-01-19]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000218	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000598	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000465	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0001840	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000006	OMIM:601680	IEA					I	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000303	OMIM:601680	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000325	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:601680	Arthrogryposis, distal, type 2B		HP:0000347	OMIM:601680	IEA					P	HPO:iea[2009-02-17]
OMIM:175400	Polyposis, intestinal, scattered and discrete		HP:0005238	OMIM:175400	IEA					P	HPO:iea[2009-02-17]
OMIM:175400	Polyposis, intestinal, scattered and discrete		HP:0000006	OMIM:175400	IEA					I	HPO:iea[2009-02-17]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0001276	PMID:38013626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0003596	PMID:38014483	PCS		1/7			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0001272	PMID:38014483;PMID:36047608	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0001250	PMID:38013626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0002066	PMID:38014483;PMID:36047608	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0002061	PMID:38014483;PMID:36047608;PMID:38013626	PCS		12/15			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0100543	PMID:38014483;PMID:36047608;PMID:38013626	PCS		3/14			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0011463	PMID:38014483	PCS		1/7			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0011462	PMID:38014483;PMID:36047608;PMID:38013626	PCS		6/15			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0001320	PMID:38014483	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0033715	PMID:38013626	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0003621	PMID:38014483;PMID:36047608;PMID:38013626	PCS		7/15			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0003487	PMID:38014483;PMID:36047608;PMID:38013626	PCS		10/16			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0002395	PMID:38014483;PMID:36047608;PMID:38013626	PCS		14/16			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0001260	PMID:38014483;PMID:36047608;PMID:38013626	PCS		4/15			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0002174	PMID:36047608	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0002172	PMID:38013626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0002070	PMID:38014483;PMID:36047608	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0031993	PMID:38013626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0011449	PMID:38013626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0011448	PMID:38013626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0007350	PMID:36047608;PMID:38013626	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0000007	PMID:36047608	PCS					I	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0000505	PMID:38013626	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0002505	PMID:38013626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620666	Spastic ataxia 10, autosomal recessive		HP:0006986	PMID:36047608	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:138500	Glycinuria with or without oxalate urolithiasis		HP:0008672	OMIM:138500	TAS					P	HPO:probinson[2014-05-24]
OMIM:138500	Glycinuria with or without oxalate urolithiasis		HP:0003108	OMIM:138500	TAS					P	HPO:probinson[2009-02-17]
OMIM:138500	Glycinuria with or without oxalate urolithiasis		HP:0000006	OMIM:138500	TAS					I	HPO:probinson[2009-02-17]
OMIM:619781	Myopia 28, autosomal recessive		HP:0000541	PMID:33456446;PMID:26957899	PCS		2/3			P	HPO:probinson[2022-05-28]
OMIM:619781	Myopia 28, autosomal recessive		HP:0000518	PMID:33456446	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:619781	Myopia 28, autosomal recessive		HP:0011463	PMID:26957899	PCS		2/2			C	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:619781	Myopia 28, autosomal recessive		HP:0000007	PMID:26957899	PCS					I	HPO:probinson[2022-05-28]
OMIM:619781	Myopia 28, autosomal recessive		HP:0011003	PMID:33456446;PMID:26957899	PCS		3/3			P	HPO:probinson[2022-05-28]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0004322	PMID:32755715	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0002970	OMIM:617974	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0002750	PMID:32755715	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0003593	PMID:32755715	PCS		1/1			C	HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0100255	PMID:32755715	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0002829	OMIM:617974	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0000926	OMIM:617974	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0002979	PMID:32755715	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0002515	PMID:32755715	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0008833	PMID:32755715	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0004349	PMID:32755715	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0001216	OMIM:617974	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617974	Spondyloepimetaphyseal dysplasia, DI Rocco type		HP:0000006	PMID:32755715	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-03]
OMIM:619959	ACCES syndrome		HP:0003577	PMID:28110515;PMID:31587267;PMID:32758660	PCS		3/3			C	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000486	PMID:28110515;PMID:32758660	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000085	PMID:31587267	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0001270	PMID:28110515	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0001508	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0007385	PMID:28110515;PMID:31587267	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000411	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0002558	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000278	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0009921	PMID:28110515	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0002575	PMID:31587267	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0001385	PMID:28110515	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000750	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0011968	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0001263	PMID:31587267	PCS		0/1			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0100257	PMID:31587267	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0002827	PMID:28110515	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000729	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0001839	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0002209	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000348	PMID:28110515	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0004209	PMID:28110515	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0002205	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000369	PMID:32758660	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:619959	ACCES syndrome		HP:0000006	PMID:28110515	PCS					I	HPO:probinson[2022-08-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0005479	PMID:35382780	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000024	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000365	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002783	PMID:30072168	PCS		19/22			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002383	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0003593	PMID:33013854;PMID:35382780;PMID:33501616;PMID:30072168	PCS		27/44			C	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27];HPO:probinson[2022-03-27];HPO:probinson[2022-04-10];HPO:probinson[2022-04-04]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0003095	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002719	OMIM:300755	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0011463	PMID:33013854;PMID:35382780;PMID:30072168	PCS		13/43			C	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27];HPO:probinson[2022-04-10]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0001903	PMID:30072168	PCS		6/22			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0003729	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0100806	PMID:33013854	PCS		16/19			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000999	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0001648	OMIM:300755	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0006532	PMID:33013854;PMID:35382780	PCS		15/21			P	HPO:probinson[2022-03-27];HPO:probinson[2022-04-10]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0410303	PMID:33501616	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002732	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0003623	PMID:33013854	PCS		1/19			C	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0001402	PMID:33013854	PCS	HP:0011462	1/19			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0004315	PMID:35382780;PMID:33501616	PCS		2/3			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-04]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0001287	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002850	PMID:35382780;PMID:33501616	PCS		3/3			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-04]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0005403	PMID:33501616	PCS		0/1			P	HPO:probinson[2022-04-04]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000010	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0003621	PMID:33013854;PMID:30072168	PCS		3/41			C	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000750	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0004432	PMID:30072168	PCS		22/22			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0011946	PMID:35382780	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002110	PMID:33013854	PCS		11/19			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000031	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0030828	PMID:35382780	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0010976	PMID:33013854;PMID:35382780;PMID:33501616;PMID:30072168	PCS		44/44			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27];HPO:probinson[2022-03-27];HPO:probinson[2022-04-10];HPO:probinson[2022-04-04]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0011108	PMID:33013854	PCS		13/19			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0001419	PMID:7722175	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000509	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0000403	PMID:33013854;PMID:30072168	PCS		23/41			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0001412	OMIM:300755	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002720	PMID:35382780;PMID:33501616	PCS		2/3			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-04]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0002028	PMID:30072168	PCS		8/22			P	HPO:probinson[2022-03-27]
OMIM:300755	Agammaglobulinemia, X-linked		HP:0001875	PMID:30072168	PCS		9/22			P	HPO:probinson[2022-03-27]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001771	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0010628	OMIM:608840	IEA					P	HPO:iea[2009-02-17]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0003236	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0004322	OMIM:608840	IEA					P	HPO:iea[2009-02-17]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0002365	OMIM:608840	IEA					P	HPO:iea[2009-02-17]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001252	PMID:12966029	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0003593	PMID:12966029	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001290	OMIM:608840	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001270	OMIM:608840	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0002518	PMID:12966029	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0025336	PMID:12966029	PCS		1/1			P	HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0003701	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001302	PMID:12966029	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0000158	PMID:12966029	PCS		0/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0000654	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001321	OMIM:608840	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0003487	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0031936	PMID:12966029	PCS		1/1			P	HPO:probinson[2022-09-23];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0002395	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001263	PMID:12966029	PCS	HP:0003593	1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0003560	PMID:12966029	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0009473	OMIM:608840	IEA					P	HPO:iea[2009-02-17]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0008981	PMID:12966029	PCS		1/1			P	HPO:probinson[2022-09-23];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0000007	OMIM:608840	IEA					I	HPO:iea[2009-02-17]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0003712	PMID:12966029	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0001335	PMID:12966029	PCS		1/1			P	HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0002987	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0000666	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0002269	PMID:12966029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:608840	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6		HP:0003458	OMIM:608840	IEA					P	HPO:iea[2009-02-17]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0005864	PMID:32181939	PCS		2/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0000365	PMID:32181939	PCS		1/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0031429	PMID:32181939	PCS		1/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0004322	PMID:32181939	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0031936	PMID:32181939	PCS		2/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0003100	PMID:32181939	PCS		3/3			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0004363	PMID:32181939	PCS		0/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0011463	PMID:32181939	PCS		1/3			C	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0011461	PMID:32181939	PCS		2/3			C	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0000007	PMID:32181939	PCS					I	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0006487	PMID:32181939	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0000703	PMID:32181939	PCS		0/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0002757	PMID:32181939	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0100529	PMID:32181939	PCS		0/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0001511	PMID:32181939	PCS		2/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0002645	PMID:32181939	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0004349	PMID:32181939	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0002753	PMID:32181939	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0005877	PMID:32181939	PCS		1/3			P	HPO:probinson[2022-05-14]
OMIM:619795	Osteogenesis imperfecta, type XXII		HP:0005855	PMID:32181939	PCS		1/3			P	HPO:probinson[2022-05-14]
OMIM:617960	Spermatogenic failure 25		HP:0030974	PMID:26199321	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-25]
OMIM:617960	Spermatogenic failure 25		HP:0011462	PMID:26199321	PCS		3/3			C	HPO:probinson[2023-03-25]
OMIM:617960	Spermatogenic failure 25		HP:0003251	PMID:26199321	PCS		3/3			P	HPO:probinson[2023-03-25]
OMIM:617960	Spermatogenic failure 25		HP:0000007	PMID:26199321	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:617960	Spermatogenic failure 25		HP:0008734	PMID:26199321	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-25]
OMIM:617960	Spermatogenic failure 25		HP:0011961	PMID:26199321	PCS		2/3			P	HPO:probinson[2023-03-25]
OMIM:617960	Spermatogenic failure 25		HP:0031039	PMID:26199321	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0002267	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0002540	PMID:33704440	PCS		2/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0002188	PMID:33704440	PCS		1/4			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0000365	PMID:33704440	PCS		2/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0003596	PMID:33704440	PCS		1/4			C	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0001250	PMID:33704440	PCS		4/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0001252	PMID:33704440	PCS		3/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0002020	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0003593	PMID:33704440	PCS		1/4			C	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0012444	PMID:33704440	PCS		1/4			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0000716	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0100704	PMID:33704440	PCS		3/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0011463	PMID:33704440	PCS		1/4			C	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0012471	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0000675	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0001249	PMID:33704440	PCS		5/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0003623	PMID:33704440	PCS		1/4			C	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0001344	PMID:33704440	PCS		3/4			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0002079	PMID:33704440	PCS		1/4			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0011968	PMID:33704440	PCS		3/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0000194	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0011344	PMID:33704440	PCS		3/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0010536	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0002307	PMID:33704440	PCS		1/6			P	HPO:probinson[2023-01-19]
OMIM:620114	Neurodevelopmental disorder with speech impairment and with or without seizures		HP:0000006	PMID:33704440	PCS					I	HPO:probinson[2023-01-19]
OMIM:246700	Chylomicron retention disease		HP:0002014	PMID:2426307	PCS					P	HPO:skoehler[2010-06-20];HP:probinson[2019-05-23]
OMIM:246700	Chylomicron retention disease		HP:0003563	PMID:2426307	PCS					P	HPO:skoehler[2010-06-18];HP:probinson[2019-05-23]
OMIM:246700	Chylomicron retention disease		HP:0003146	PMID:2426307	PCS					P	HPO:skoehler[2010-06-18];HP:probinson[2019-05-23]
OMIM:246700	Chylomicron retention disease		HP:0002013	OMIM:246700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:246700	Chylomicron retention disease		HP:0002495	OMIM:246700	IEA					P	HPO:iea[2009-02-17]
OMIM:246700	Chylomicron retention disease		HP:0003593	OMIM:246700	IEA					C	HPO:skoehler[2010-06-19]
OMIM:246700	Chylomicron retention disease		HP:0004395	OMIM:246700	IEA					P	HPO:iea[2009-02-17]
OMIM:246700	Chylomicron retention disease		HP:0002570	PMID:2426307	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-05-23]
OMIM:246700	Chylomicron retention disease		HP:0003073	OMIM:246700	IEA					P	HPO:iea[2009-02-17]
OMIM:246700	Chylomicron retention disease		HP:0034787	PMID:2426307	PCS					P	HPO:probinson[2023-07-18]
OMIM:246700	Chylomicron retention disease		HP:0001508	OMIM:246700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:246700	Chylomicron retention disease		HP:0012153	PMID:2426307	PCS					P	HP:probinson[2019-05-23]
OMIM:246700	Chylomicron retention disease		HP:0000007	OMIM:246700	IEA					I	HPO:iea[2009-02-17]
OMIM:246700	Chylomicron retention disease		HP:0001510	OMIM:246700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:246700	Chylomicron retention disease		HP:0001249	OMIM:246700	IEA					P	HPO:iea[2009-02-17]
OMIM:246700	Chylomicron retention disease		HP:0001315	OMIM:246700	IEA					P	HPO:iea[2009-02-17]
OMIM:613737	Acne inversa, familial, 3		HP:0012322	OMIM:613737	TAS					P	HPO:probinson[2013-01-09]
OMIM:613737	Acne inversa, familial, 3		HP:0040154	PMID:20929727	PCS					P	HPO:skoehler[2015-08-05]
OMIM:613737	Acne inversa, familial, 3		HP:0011132	OMIM:613737	TAS					P	HPO:probinson[2013-08-11]
OMIM:613737	Acne inversa, familial, 3		HP:0100838	PMID:20929727	PCS					P	HPO:probinson[2013-08-11]
OMIM:613737	Acne inversa, familial, 3		HP:0000006	PMID:20929727	PCS					I	HPO:skoehler[2015-12-30]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001276	OMIM:261630	IEA					P	HPO:skoehler[2010-06-20]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0002344	OMIM:261630	IEA					P	HPO:skoehler[2010-06-20]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0000252	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0002015	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001266	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001332	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001250	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0003781	OMIM:261630	TAS					P	HPO:skoehler[2015-01-04]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001252	OMIM:261630	IEA					P	HPO:iea[2009-02-17]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001263	OMIM:261630	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0003593	OMIM:261630	IEA					C	HPO:skoehler[2010-06-19]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:6000966	PMID:7110817	PCS		2/2			P	HPO:probinson[2024-08-03]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0000737	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0003828	OMIM:261630	IEA					M	HPO:skoehler[2010-06-19]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0000007	OMIM:261630	IEA					I	HPO:iea[2009-02-17]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001954	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0004923	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0002514	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001249	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001337	OMIM:261630	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261630	Hyperphenylalaninemia, bh4-deficient, C		HP:0001336	OMIM:261630	IEA					P	HPO:iea[2009-02-17]
OMIM:615346	Precocious puberty, central, 2		HP:0012275	PMID:26431553	PCS					I	HPO:probinson[2019-09-07]
OMIM:615346	Precocious puberty, central, 2		HP:0005616	PMID:23738509	PCS					P	HPO:skoehler[2013-08-18];HPO:probinson[2019-09-07]
OMIM:615346	Precocious puberty, central, 2		HP:0012411	PMID:23738509	PCS					P	HPO:probinson[2019-09-07]
OMIM:615346	Precocious puberty, central, 2		HP:0010314	PMID:26431553	PCS			FEMALE		P	HPO:skoehler[2013-08-18];HPO:probinson[2019-09-07]
OMIM:618662	Diarrhea 11, malabsorptive, congenital		HP:0002014	PMID:31217582	IEA	HP:0003577	9/9			P	HPO:probinson[2020-07-20]
OMIM:618662	Diarrhea 11, malabsorptive, congenital		HP:0011473	PMID:31217582	PCS		3/9			P	HPO:probinson[2020-07-20]
OMIM:618662	Diarrhea 11, malabsorptive, congenital		HP:0000007	PMID:31217582	PCS					I	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:608471	Corneal dystrophy, lattice type IIIA		HP:0003584	PMID:9497262	PCS		9/9			C	HPO:probinson[2023-04-22]
OMIM:608471	Corneal dystrophy, lattice type IIIA		HP:0007663	OMIM:608471	TAS					P	HPO:skoehler[2015-07-26]
OMIM:608471	Corneal dystrophy, lattice type IIIA		HP:0000505	OMIM:608471	IEA					P	HPO:iea[2009-02-17]
OMIM:608471	Corneal dystrophy, lattice type IIIA		HP:0000006	PMID:9497262	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-22]
OMIM:608471	Corneal dystrophy, lattice type IIIA		HP:0200020	OMIM:608471	TAS					P	HPO:probinson[2012-07-16]
OMIM:608471	Corneal dystrophy, lattice type IIIA		HP:0001149	PMID:9497262	PCS		9/9			P	HPO:iea[2009-02-17]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0002265	OMIM:616897	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0005257	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001371	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0003196	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0100333	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0031107	OMIM:616897	TAS					P	HPO:probinson[2018-03-05]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0011220	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000316	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000358	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000252	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000054	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000175	OMIM:616897	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001541	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0004331	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001181	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000926	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000007	PMID:26365339	PCS					I	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000047	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000248	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000369	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000126	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0005855	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0003015	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0002202	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0002089	OMIM:616897	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000463	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001195	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0003097	OMIM:616897	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0012368	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001629	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000938	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001789	OMIM:616897	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0002119	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000773	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0009826	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001561	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000431	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001640	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001321	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000470	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001518	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000506	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001639	OMIM:616897	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0006640	PMID:26365339	PCS		20/20			P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0003978	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0001511	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0002645	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000465	OMIM:616897	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		HP:0000347	PMID:26365339	PCS					P	HPO:probinson[2017-06-26]
OMIM:617237	Immunodeficiency 49		HP:0003577	PMID:27959755	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0000582	OMIM:617237	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617237	Immunodeficiency 49		HP:0001250	PMID:27959755	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0001274	PMID:27959755	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0001252	PMID:27959755	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0001290	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0012745	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0031545	PMID:27959755	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0000316	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0001888	OMIM:617237	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617237	Immunodeficiency 49		HP:0001007	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0003347	PMID:27959755	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0001249	PMID:27959755	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0000358	OMIM:617237	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617237	Immunodeficiency 49		HP:0003765	PMID:27959755	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0004415	PMID:27959755	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0000973	OMIM:617237	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617237	Immunodeficiency 49		HP:0002058	OMIM:617237	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617237	Immunodeficiency 49		HP:0005403	PMID:27959755	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0001880	OMIM:617237	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617237	Immunodeficiency 49		HP:0002510	PMID:27959755	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0001344	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0000695	PMID:27959755	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0004430	PMID:27959755	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0001263	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0034295	PMID:27959755	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0001537	PMID:27959755	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0002645	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617237	Immunodeficiency 49		HP:0000322	OMIM:617237	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617237	Immunodeficiency 49		HP:0000006	PMID:27959755	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617237	Immunodeficiency 49		HP:0000347	OMIM:617237	TAS					P	HPO:skoehler[2017-07-13]
OMIM:116400	Cataract, nuclear total		HP:0100018	PMID:23531866	PCS	HP:0003577				P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-15]
OMIM:116400	Cataract, nuclear total		HP:0000006	PMID:23531866	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0000365	OMIM:601455	IEA					P	HPO:probinson[2009-02-17]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0003693	PMID:24136616	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0002460	PMID:24136616	PCS		2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0034337	PMID:24136616	PCS		2/3			P	HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0001270	PMID:24136616	PCS		2/2			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0011463	PMID:24136616	PCS		3/3			C	HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0002936	PMID:24136616	PCS		2/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0002317	PMID:24136616	PCS		1/2			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0002359	PMID:24136616	PCS		1/3			P	HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0003701	PMID:24136616	PCS		2/2			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0003447	OMIM:601455	IEA					P	HPO:probinson[2009-02-17]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0001765	PMID:24136616	PCS		2/3			P	HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0001265	OMIM:601455	IEA					P	HPO:probinson[2009-02-17]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0002751	PMID:24136616	PCS		1/2			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0006858	PMID:24136616	PCS		1/1			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0006958	OMIM:601455	TAS					P	HPO:probinson[2012-03-18]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0001288	PMID:24136616	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0001761	PMID:24136616	PCS		2/2			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0004696	OMIM:601455	IEA					P	HPO:probinson[2009-02-17]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0006937	PMID:24136616	PCS		1/1			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0006916	OMIM:601455	IEA					P	HPO:probinson[2009-02-17]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0003383	OMIM:601455	IEA					P	HPO:probinson[2009-02-17]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0001284	PMID:24136616	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0003481	OMIM:601455	TAS					P	HPO:probinson[2012-03-18]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0000649	OMIM:601455	TAS					P	HPO:probinson[2012-03-18]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0000407	PMID:24136616	PCS		3/3			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0000007	PMID:10831399	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0000762	PMID:24136616	PCS		2/2			P	HPO:probinson[2012-03-18];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0006886	PMID:24136616	PCS		1/1			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0000501	PMID:24136616	PCS		2/3			P	HPO:probinson[2023-05-10]
OMIM:601455	Charcot-Marie-Tooth disease, type 4D		HP:0000545	PMID:24136616	PCS		1/2			P	HPO:probinson[2023-05-10];HPO:probinson[2023-05-10]
OMIM:192700	Venular insufficiency, systemic		HP:0001626	OMIM:192700	IEA					P	HPO:iea[2009-02-17]
OMIM:192700	Venular insufficiency, systemic		HP:0000961	OMIM:192700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:192700	Venular insufficiency, systemic		HP:0000006	PMID:13561707;PMID:14117628	TAS		20/20			I	HPO:nvasilevsky[2019-03-12];HPO:nvasilevsky[2019-03-12];HPO:nvasilevsky[2019-03-12]
OMIM:615420	Myopia 22, autosomal dominant		HP:0007663	OMIM:615420	TAS		1/8			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-12]
OMIM:615420	Myopia 22, autosomal dominant		HP:0011003	PMID:23579484	PCS		8/8			P	HPO:probinson[2023-02-12]
OMIM:615420	Myopia 22, autosomal dominant		HP:0000006	PMID:23579484	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-12]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001276	PMID:12594532	PCS		1/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001254	PMID:12594532	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001289	OMIM:237310	IEA					P	HPO:iea[2009-02-17]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0002045	PMID:12594532	PCS		1/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0002013	OMIM:237310	TAS		1/3			P	HPO:skoehler[2009-02-17]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0003572	PMID:12594532	PCS		2/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0002098	PMID:12594532	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001250	PMID:12594532	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0100543	OMIM:237310	TAS					P	HPO:skoehler[2009-02-17]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001948	PMID:12594532	PCS		1/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001508	PMID:12594532	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0000718	OMIM:237310	IEA					P	HPO:iea[2009-02-17]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0000007	PMID:12594532	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0020221	PMID:12594532	PCS		1/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001987	PMID:12594532	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0500149	PMID:7623444	PCS		2/2			P	HPO:NicoleVasilevsky[2018-02-23];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0003217	PMID:12594532	PCS		3/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:6000161	PMID:12594532	PCS		1/1			P	HPO:probinson[2024-01-13];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0002789	PMID:12594532	PCS		1/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0002039	PMID:12594532	PCS		1/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0001259	PMID:12594532	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:237310	N-acetylglutamate synthase deficiency		HP:0003348	PMID:12594532	PCS		1/3			P	HPO:probinson[2024-01-13]
OMIM:237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0003623	PMID:12594532	PCS		3/3			C	HPO:probinson[2024-01-13]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000286	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0003577	PMID:17985375	PCS		20/20			C	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000189	OMIM:605627	TAS					P	HPO:skoehler[2013-08-18]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000343	PMID:17985375	PCS		11/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000463	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0001250	PMID:17985375	PCS		7/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0003196	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0012806	PMID:17985375	PCS		20/20			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0010806	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0002084	PMID:17985375	PCS		8/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0045075	PMID:17985375	PCS		20/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0011220	OMIM:605627	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000316	PMID:17985375	PCS		19/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000238	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000337	PMID:17985375	PCS		20/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000612	PMID:17985375	PCS		2/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0001305	PMID:17985375	PCS		1/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0008897	PMID:17985375	PCS		16/19			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0002119	PMID:17985375	PCS		16/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000218	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0002714	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000653	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000256	PMID:17985375	PCS		10/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0006315	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000358	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0001249	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0001320	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0001363	OMIM:605627	IEA		3/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000175	OMIM:605627	IEA		12/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0002079	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0001162	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000050	PMID:17985375	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0001263	PMID:17985375	PCS		20/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000272	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0032327	PMID:17985375	PCS		1/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0100259	PMID:17985375	PCS		1/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000609	PMID:17985375	PCS		6/7			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0009891	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000528	PMID:17985375	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000508	PMID:17985375	PCS		4/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000426	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000405	PMID:17985375	PCS		1/20			P	HPO:probinson[2022-05-08]
OMIM:605627	Cerebrooculonasal syndrome		HP:0002007	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000289	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000369	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000248	OMIM:605627	IEA					P	HPO:iea[2009-02-17]
OMIM:605627	Cerebrooculonasal syndrome		HP:0000006	OMIM:605627	IEA					I	HPO:iea[2009-02-17]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0001696	PMID:23849777	PCS		2/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0002110	PMID:23849777	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0033036	PMID:23849777	PCS		1/1			P	HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0012207	PMID:23849777	PCS		1/1			P	HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0031245	PMID:23849777	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0002719	PMID:23849777	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0011462	PMID:23849777	PCS		3/4			C	HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0000007	PMID:23849777	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0007663	PMID:23849777	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0007401	PMID:23849777	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0000543	PMID:23849777	PCS		1/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0007787	PMID:23849777	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0000510	PMID:23849777	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0001742	PMID:23849777	PCS		1/4			P	HPO:probinson[2023-03-21]
OMIM:615434	Retinitis pigmentosa with or without situs inversus		HP:0003623	PMID:23849777	PCS		1/4			C	HPO:probinson[2023-03-21]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000286	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000343	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000023	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000160	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000581	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0012745	OMIM:277720	TAS					P	HPO:skoehler[2014-03-24]
OMIM:277720	Whistling face syndrome, recessive form		HP:0009465	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000316	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000218	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0002751	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0001762	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000211	OMIM:277720	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000430	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0003044	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000171	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000272	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000470	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0011800	OMIM:277720	TAS					P	HPO:skoehler[2015-11-15]
OMIM:277720	Whistling face syndrome, recessive form		HP:0010751	OMIM:277720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277720	Whistling face syndrome, recessive form		HP:0012385	OMIM:277720	TAS					P	HPO:skoehler[2013-10-22]
OMIM:277720	Whistling face syndrome, recessive form		HP:0006380	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000506	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000508	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000426	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000007	OMIM:277720	IEA					I	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0002987	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000347	OMIM:277720	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277720	Whistling face syndrome, recessive form		HP:0000346	OMIM:277720	IEA					P	HPO:iea[2009-02-17]
OMIM:618110	Spermatogenic failure 30		HP:0030974	PMID:28536242	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:618110	Spermatogenic failure 30		HP:0003251	PMID:28536242	PCS		5/5			P	HPO:probinson[2023-02-25]
OMIM:618110	Spermatogenic failure 30		HP:0011462	PMID:28536242	PCS		5/5			C	HPO:probinson[2023-02-25];HPO:probinson[2023-02-25]
OMIM:618110	Spermatogenic failure 30		HP:0000007	PMID:28536242	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:618110	Spermatogenic failure 30		HP:0031038	PMID:28536242	PCS		3/3			P	HPO:probinson[2023-02-25]
OMIM:618110	Spermatogenic failure 30		HP:0000028	PMID:28536242	PCS		2/5			P	HPO:probinson[2023-02-25]
OMIM:618110	Spermatogenic failure 30		HP:0000027	PMID:28536242	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617223	Sudden cardiac failure, alcohol-induced		HP:0003621	PMID:27523597	PCS					C	HPO:probinson[2023-03-03]
OMIM:617223	Sudden cardiac failure, alcohol-induced		HP:0001685	PMID:27523597	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:617223	Sudden cardiac failure, alcohol-induced		HP:0000007	PMID:27523597	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:617223	Sudden cardiac failure, alcohol-induced		HP:0100749	PMID:27523597	PCS				HP:0025211	P	HPO:probinson[2023-03-03]
OMIM:225700	Encephalomalacia, multilocular		HP:0000252	OMIM:225700	IEA					P	HPO:iea[2009-02-17]
OMIM:225700	Encephalomalacia, multilocular		HP:0001264	OMIM:225700	IEA					P	HPO:iea[2009-02-17]
OMIM:225700	Encephalomalacia, multilocular		HP:0040197	OMIM:225700	IEA					P	HPO:skoehler[2015-12-30]
OMIM:225700	Encephalomalacia, multilocular		HP:0000007	OMIM:225700	IEA					I	HPO:iea[2009-02-17]
OMIM:225700	Encephalomalacia, multilocular		HP:0001249	OMIM:225700	IEA					P	HPO:iea[2009-02-17]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0002003	OMIM:600987	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000341	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0003577	PMID:25712757	PCS		1/1			C	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0010804	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000582	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0004322	OMIM:600987	TAS					P	HPO:probinson[2009-02-17]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0002020	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0012725	OMIM:600987	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0045075	OMIM:600987	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0012523	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0001629	OMIM:600987	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0010055	OMIM:600987	TAS					P	HPO:probinson[2012-06-08]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0033255	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0011682	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000219	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0001249	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0002553	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000175	PMID:25712757	PCS		1/1			P	HPO:probinson[2012-06-08];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000252	OMIM:600987	IEA					P	HPO:iea[2009-02-17]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0001684	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0002571	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0011968	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000490	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0001263	OMIM:600987	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0001680	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0004691	PMID:25712757	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0011344	PMID:25712757	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0011304	OMIM:600987	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0009890	OMIM:600987	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000729	PMID:25712757	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0011230	PMID:25712757	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0009237	OMIM:600987	TAS					P	HPO:probinson[2012-06-08]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0001852	PMID:25712757	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0001631	OMIM:600987	IEA					P	HPO:iea[2009-02-17]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0009536	OMIM:600987	TAS					P	HPO:probinson[2012-06-08]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000006	OMIM:600987	IEA					I	HPO:iea[2009-02-17]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000204	OMIM:600987	TAS					P	HPO:probinson[2009-02-17]
OMIM:600987	Cleft palate, cardiac defects, and impaired intellectual development		HP:0000369	OMIM:600987	IEA					P	HPO:skoehler[2019-09-07]
OMIM:611134	Meckel syndrome, type 4		HP:0000252	OMIM:611134	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0000175	OMIM:611134	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0002323	OMIM:611134	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0002079	PMID:17564974	PCS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0001162	OMIM:611134	TAS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0002084	OMIM:611134	TAS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0001629	PMID:17564974	PCS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0001408	OMIM:611134	TAS					P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0000107	OMIM:611134	TAS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0000007	PMID:17564974	PCS					I	HPO:probinson[2013-01-09]
OMIM:611134	Meckel syndrome, type 4		HP:0001305	PMID:17564974	PCS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0000568	OMIM:611134	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0000238	OMIM:611134	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0002419	OMIM:611134	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0006487	OMIM:611134	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0001511	OMIM:611134	TAS					P	HPO:skoehler[2015-04-26]
OMIM:611134	Meckel syndrome, type 4		HP:0001631	PMID:17564974	PCS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0002335	PMID:17564974	PCS					P	HPO:probinson[2013-04-01]
OMIM:611134	Meckel syndrome, type 4		HP:0002435	OMIM:611134	IEA					P	HPO:skoehler[2018-10-08]
OMIM:168860	Patella aplasia-hypoplasia		HP:0003065	OMIM:168860	IEA					P	HPO:iea[2009-02-17]
OMIM:168860	Patella aplasia-hypoplasia		HP:0006443	OMIM:168860	IEA					P	HPO:iea[2009-02-17]
OMIM:168860	Patella aplasia-hypoplasia		HP:0000006	OMIM:168860	IEA					I	HPO:iea[2009-02-17]
OMIM:168860	Patella aplasia-hypoplasia		HP:0000951	OMIM:168860	IEA					P	HPO:iea[2009-02-17]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003202	PMID:21109228	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003236	PMID:21109228	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003324	PMID:21109228	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0001371	PMID:21109228	PCS	HP:0003584				P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003551	PMID:21109228	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003560	PMID:21109228	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0001270	PMID:21109228	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003391	PMID:21109228	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0011463	PMID:21109228	PCS					C	HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0002938	PMID:21109228	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0000007	PMID:21109228	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003701	PMID:21109228	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:613723	Muscular dystrophy, limb-girdle, type 2Q		HP:0003678	PMID:21109228	PCS					C	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-23]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0003236	PMID:23768512	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0000252	PMID:23768512	PCS		2/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0003577	PMID:23768512	PCS		1/3			C	HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0001250	PMID:23768512	PCS		2/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0030046	PMID:23768512	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0001252	PMID:23768512	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0003560	PMID:23768512	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0001270	OMIM:615352	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0002093	PMID:23768512	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0000518	PMID:23768512	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0000639	PMID:23768512	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0011463	PMID:23768512	PCS		2/3			C	HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0000007	PMID:23768512	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0001638	PMID:23768512	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0003701	OMIM:615352	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0003325	PMID:23768512	PCS		3/3			P	HPO:probinson[2022-12-13]
OMIM:615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14		HP:0003546	PMID:23768512	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-13]
OMIM:221200	Deafness and myopia		HP:0003577	PMID:23543054	PCS		1/7			C	HPO:probinson[2023-02-06]
OMIM:221200	Deafness and myopia		HP:0000407	PMID:23543054	PCS		7/7			P	HPO:probinson[2023-02-06]
OMIM:221200	Deafness and myopia		HP:0003593	PMID:23543054	PCS		6/7			C	HPO:probinson[2023-02-06]
OMIM:221200	Deafness and myopia		HP:0000007	PMID:23543054	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-06]
OMIM:221200	Deafness and myopia		HP:0011003	PMID:23543054	PCS		7/7			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-06]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001342	PMID:31836668	PCS		2/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0002840	PMID:32092142	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001321	PMID:31836668	PCS		1/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001640	PMID:32092142	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001250	PMID:31836668	PCS		1/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001263	PMID:31836668	PCS		2/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0000093	PMID:31836668	PCS		2/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0003281	PMID:31836668	PCS					P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0002093	PMID:32092142	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0033106	PMID:31836668	PCS		2/2			P	HPO:probinson[2020-10-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001919	PMID:31836668	PCS		1/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001903	PMID:32092142	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001905	PMID:31836668	PCS	HP:0003577	1/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0000822	PMID:31836668	PCS					P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0000007	PMID:31836668	PCS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001954	PMID:31836668	PCS		1/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001522	PMID:31836668	PCS		2/2			C	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0002514	PMID:31836668;PMID:32092142	PCS		3/3			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0002104	PMID:31836668	PCS		2/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0002500	PMID:31836668	PCS		2/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001622	PMID:31836668	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-12]
OMIM:618886	Pseudo-Torch syndrome 3		HP:0001974	PMID:32092142	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:610202	Cataract 21, multiple types		HP:0007957	PMID:11772997	PCS		1/10			P	HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0003621	PMID:11772997	PCS		7/8			C	HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0003577	PMID:11772997	PCS		1/8			C	HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0000541	OMIM:610202	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:610202	Cataract 21, multiple types		HP:0007780	PMID:11772997	PCS	HP:0003621	7/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0000482	PMID:11772997	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0000612	PMID:11772997	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0000659	PMID:11772997	PCS		1/10			P	HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0011003	PMID:11772997	PCS		1/10			P	HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0001104	OMIM:610202	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:610202	Cataract 21, multiple types		HP:0000006	PMID:11772997	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-18]
OMIM:610202	Cataract 21, multiple types		HP:0007976	OMIM:610202	IEA					P	HPO:iea[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0000882	OMIM:269250	TAS					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0001156	OMIM:269250	IEA					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0005257	PMID:17952091	PCS		2/2			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0003196	PMID:17952091	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0001790	PMID:17952091	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0031026	PMID:17952091	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0008450	PMID:17952091	PCS		1/1			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0011461	PMID:17952091	PCS		2/2			C	HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0008873	OMIM:269250	TAS					P	HPO:iea[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0003826	OMIM:269250	TAS					C	HPO:skoehler[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0000895	OMIM:269250;PMID:27666822	PCS		20/20			P	HPO:lccarmody[2018-09-26];HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0000774	PMID:17952091	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0000256	OMIM:269250	TAS					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0000773	OMIM:269250	TAS					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0003026	PMID:17952091	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0000175	OMIM:269250	TAS					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0009826	PMID:17952091	PCS		2/2			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0001561	OMIM:269250	TAS					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0003025	OMIM:269250	IEA					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0003300	PMID:17952091	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0004233	OMIM:269250	IEA					P	HPO:iea[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0000272	OMIM:269250	TAS					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0000470	OMIM:269250	TAS					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0011800	PMID:17952091	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0003180	PMID:17952091	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0000907	OMIM:269250	TAS					P	HPO:iea[2012-07-29]
OMIM:269250	Schneckenbecken dysplasia		HP:0000947	OMIM:269250	IEA					P	HPO:probinson[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0000926	PMID:17952091	PCS		1/1			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0001537	PMID:17952091	PCS		1/1			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0000007	PMID:17952091	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0001538	PMID:17952091	PCS		1/1			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:269250	Schneckenbecken dysplasia		HP:0008108	OMIM:269250	IEA					P	HPO:iea[2009-02-17]
OMIM:269250	Schneckenbecken dysplasia		HP:0001776	PMID:17952091	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:312190	Radial aplasia, X-linked		HP:0002023	OMIM:312190	IEA					P	HPO:iea[2009-02-17]
OMIM:312190	Radial aplasia, X-linked		HP:0003244	OMIM:312190	IEA					P	HPO:iea[2009-02-17]
OMIM:312190	Radial aplasia, X-linked		HP:0000238	OMIM:312190	IEA					P	HPO:iea[2009-02-17]
OMIM:312190	Radial aplasia, X-linked		HP:0001417	OMIM:312190	IEA					I	HPO:iea[2009-02-17]
OMIM:312190	Radial aplasia, X-linked		HP:0003974	OMIM:312190	IEA					P	HPO:iea[2009-02-17]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0002465	OMIM:614702	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0003577	PMID:22608499	PCS		2/3			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0002202	PMID:22608499	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001332	OMIM:614702	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001250	OMIM:614702	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001252	PMID:22608499	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0003593	PMID:22608499	PCS		1/3			C	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001508	OMIM:614702	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001987	PMID:22608499	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001943	PMID:22608499	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001942	PMID:22608499	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0003348	OMIM:614702	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0003128	PMID:22608499	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001562	PMID:22608499	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001541	PMID:22608499	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001662	PMID:22608499	PCS		3/3			P	HPO:probinson[2023-02-21];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001640	PMID:22608499	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0011924	PMID:22608499	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0011968	PMID:22608499	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001263	OMIM:614702	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0002151	PMID:22608499	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001639	PMID:22608499	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001518	OMIM:614702	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0000007	PMID:22608499	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0000648	PMID:22608499	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001511	PMID:22608499	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001698	PMID:22608499	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:614702	Combined oxidative phosphorylation deficiency 10		HP:0001257	OMIM:614702	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003236	PMID:21953594;PMID:24957499	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-07];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0001250	PMID:21953594	PCS		4/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003551	PMID:21953594;PMID:24957499	PCS		3/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-07];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0001270	PMID:21953594	PCS		1/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003391	PMID:21953594;PMID:24957499	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-07];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:6000659	PMID:21953594	PCS					P	HPO:probinson[2024-04-03]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0007141	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0011463	PMID:21953594	PCS		1/5			C	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0040078	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0009046	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0008994	PMID:21953594;PMID:24957499	PCS		6/6			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0002515	PMID:21953594	PCS		1/5			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003722	PMID:21953594	PCS		1/5			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003621	PMID:21953594	PCS		1/5			C	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0031936	PMID:21953594	PCS		1/5			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003581	PMID:21953594	PCS		3/5			C	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0001284	PMID:24957499	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0031237	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0002808	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0008981	PMID:21953594	PCS		3/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0000007	PMID:21953594	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0000762	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0002987	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0002500	PMID:21953594;PMID:24957499	PCS		6/6			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003710	PMID:21953594	PCS		1/5			P	HPO:probinson[2021-02-07]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003677	PMID:21953594	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-21]
OMIM:618138	Muscular dystrophy, limb-girdle, autosomal recessive 23		HP:0003557	PMID:24957499	PCS		1/1			P	HPO:probinson[2021-02-07]
OMIM:616115	Familial cold autoinflammatory syndrome 4		HP:0001025	PMID:25385754	PCS				HP:0025206	P	HPO:probinson[2020-09-27]
OMIM:616115	Familial cold autoinflammatory syndrome 4		HP:0002829	PMID:25385754	PCS				HP:0025206	P	HPO:skoehler[2015-01-04];HPO:probinson[2020-09-27]
OMIM:616115	Familial cold autoinflammatory syndrome 4		HP:0003593	PMID:25385754	PCS					C	HPO:probinson[2020-09-27]
OMIM:616115	Familial cold autoinflammatory syndrome 4		HP:0001945	PMID:25385754	PCS				HP:0025206	P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-27]
OMIM:616115	Familial cold autoinflammatory syndrome 4		HP:0000006	PMID:25385754	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-27]
OMIM:619226	Blistering, acantholytic, of oral and laryngeal mucosa		HP:0000007	PMID:30528827	PCS					I	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619226	Blistering, acantholytic, of oral and laryngeal mucosa		HP:0031446	PMID:30528827	PCS	HP:0003577	1/1		HP:0031796	P	HPO:probinson[2021-05-29]
OMIM:619226	Blistering, acantholytic, of oral and laryngeal mucosa		HP:0200097	PMID:30528827	PCS	HP:0003577	1/1		HP:0031796	P	HPO:probinson[2021-05-29]
OMIM:232240	Glycogen storage disease Ic		HP:0002884	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0003077	OMIM:232240	TAS					P	HPO:probinson[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0000083	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0002240	PMID:9686363	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0410175	OMIM:232240	IEA					P	HPO:skoehler[2018-10-08]
OMIM:232240	Glycogen storage disease Ic		HP:0012522	OMIM:232240	TAS					P	HPO:probinson[2014-01-01]
OMIM:232240	Glycogen storage disease Ic		HP:0001943	PMID:9686363	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0001946	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0001942	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0001402	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0003128	PMID:9686363	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0003623	PMID:9686363	PCS		1/1			C	HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0002037	PMID:9686363	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0000991	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0000097	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0000790	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0000093	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0002092	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0012213	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0006280	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0040289	PMID:9686363	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0010280	PMID:9686363	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0000822	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0000007	OMIM:232240	IEA					I	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0000823	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0002788	PMID:9686363	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:232240	Glycogen storage disease Ic		HP:0001114	OMIM:232240	TAS					P	HPO:skoehler[2017-07-13]
OMIM:232240	Glycogen storage disease Ic		HP:0002723	PMID:9686363	PCS		0/1			P	HPO:probinson[2024-03-08]
OMIM:232240	Glycogen storage disease Ic		HP:0001997	OMIM:232240	IEA					P	HPO:iea[2009-02-17]
OMIM:232240	Glycogen storage disease Ic		HP:0002149	OMIM:232240	IEA					P	HPO:skoehler[2019-02-22]
OMIM:619232	Bile acid conjugation defect 1		HP:0003621	PMID:23415802	PCS		3/7			C	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0031956	PMID:23415802	PCS		3/7			P	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0001399	PMID:23415802	PCS		1/7			P	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0002908	PMID:23415802	PCS		1/7			P	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0011463	PMID:23415802	PCS		1/7			C	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0003593	PMID:23415802	PCS		3/7			C	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0002240	PMID:23415802	PCS		1/7			P	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0002748	PMID:23415802	PCS		2/7			P	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0000007	PMID:23415802	PCS					I	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0000952	PMID:23415802	PCS		7/7			P	HPO:probinson[2021-05-09]
OMIM:619232	Bile acid conjugation defect 1		HP:0031964	PMID:23415802	PCS		3/7			P	HPO:probinson[2021-05-09]
OMIM:609021	Peripheral cone dystrophy		HP:0007769	OMIM:609021	TAS					P	HPO:probinson[2012-04-28]
OMIM:609021	Peripheral cone dystrophy		HP:0000980	OMIM:609021	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609021	Peripheral cone dystrophy		HP:0007761	OMIM:609021	TAS		2/3			P	HPO:probinson[2012-04-28]
OMIM:609021	Peripheral cone dystrophy		HP:0000007	OMIM:609021	TAS					I	HPO:probinson[2012-04-28]
OMIM:609021	Peripheral cone dystrophy		HP:0000505	OMIM:609021	TAS					P	HPO:probinson[2012-04-28]
OMIM:609021	Peripheral cone dystrophy		HP:0000648	OMIM:609021	TAS		2/3			P	HPO:probinson[2012-04-28]
OMIM:609021	Peripheral cone dystrophy		HP:0000548	OMIM:609021	IEA					P	HPO:skoehler[2015-12-30]
OMIM:609021	Peripheral cone dystrophy		HP:0000543	OMIM:609021	TAS				HP:0012825	P	HPO:probinson[2012-04-28]
OMIM:609021	Peripheral cone dystrophy		HP:0030528	OMIM:609021	IEA					P	HPO:skoehler[2018-10-08]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0003027	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0003038	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0006439	OMIM:164900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0007759	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0000485	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0002673	OMIM:164900	TAS					P	HPO:probinson[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0003042	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0012478	OMIM:164900	TAS					P	HPO:skoehler[2013-11-28]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0000618	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0006055	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0006441	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0006169	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0002986	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0000006	OMIM:164900	IEA					I	HPO:iea[2009-02-17]
OMIM:164900	Ophthalmomandibulomelic dysplasia		HP:0000765	OMIM:164900	IEA					P	HPO:iea[2009-02-17]
OMIM:613079	Deafness, autosomal recessive 77		HP:0008619	PMID:19732867	PCS	HP:0011463	7/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-04-27]
OMIM:613079	Deafness, autosomal recessive 77		HP:0001751	PMID:19732867	PCS		0/7			P	HPO:probinson[2020-04-27];HPO:probinson[2024-03-14]
OMIM:613079	Deafness, autosomal recessive 77		HP:0000360	PMID:19732867	PCS		0/7			P	HPO:probinson[2020-04-27];HPO:probinson[2024-03-14]
OMIM:613079	Deafness, autosomal recessive 77		HP:0000007	PMID:19732867	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-04-27]
OMIM:618892	Harderoporphyria		HP:0033627	PMID:7757079;PMID:31085196	PCS		13/13			P	HPO:probinson[2021-02-13];HPO:probinson[2022-12-18]
OMIM:618892	Harderoporphyria		HP:0000992	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0002013	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0003265	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0002240	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0012217	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0003281	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0034472	PMID:7757079	PCS		3/3			P	HPO:probinson[2022-12-18]
OMIM:618892	Harderoporphyria		HP:0001878	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0000007	PMID:7757079	PCS					I	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24];HPO:probinson[2022-12-18]
OMIM:618892	Harderoporphyria		HP:0000953	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0001923	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0001744	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0006579	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618892	Harderoporphyria		HP:0040318	OMIM:618892	TAS					P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0004325	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0001561	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0008935	OMIM:300580	TAS					P	HPO:probinson[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0010628	OMIM:300580	TAS					P	HPO:skoehler[2015-04-26]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0003577	PMID:16173074	PCS					C	HPO:probinson[2022-09-02]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0004322	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0002098	OMIM:300580	TAS					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0003198	OMIM:300580	TAS					P	HPO:probinson[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0002033	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0004661	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0000508	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0002747	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0001423	PMID:16173074	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0001612	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0000347	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0003755	OMIM:300580	TAS					P	HPO:probinson[2009-02-17]
OMIM:300580	Myopathy, congenital, with fiber-type disproportion, X-linked		HP:0001644	OMIM:300580	IEA					P	HPO:iea[2009-02-17]
OMIM:617592	Spermatogenic failure 19		HP:0032560	PMID:28552195	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:617592	Spermatogenic failure 19		HP:0003251	PMID:28552195	PCS		3/3			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:617592	Spermatogenic failure 19		HP:0011462	PMID:28552195	PCS		3/3			C	HPO:probinson[2022-11-08]
OMIM:617592	Spermatogenic failure 19		HP:0000007	PMID:28552195	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-08]
OMIM:617592	Spermatogenic failure 19		HP:0012207	PMID:28552195	PCS		3/3			P	HPO:probinson[2022-11-08]
OMIM:617592	Spermatogenic failure 19		HP:0032558	PMID:28552195	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:617592	Spermatogenic failure 19		HP:0032559	PMID:28552195	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:616854	Even-Plus syndrome		HP:0003510	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0006989	PMID:26598328	PCS		1/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0002023	PMID:26598328	PCS		2/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0001057	PMID:26598328	PCS		2/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000089	OMIM:616854	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616854	Even-Plus syndrome		HP:0003196	OMIM:616854	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616854	Even-Plus syndrome		HP:0001274	OMIM:616854	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616854	Even-Plus syndrome		HP:0008070	OMIM:616854	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616854	Even-Plus syndrome		HP:0000518	PMID:26598328	PCS		0/3			P	HPO:probinson[2017-06-22];HPO:probinson[2024-03-15]
OMIM:616854	Even-Plus syndrome		HP:0008551	PMID:26598328	PCS		3/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000218	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0002656	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000457	PMID:26598328	PCS		3/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000456	PMID:26598328	PCS		3/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0002553	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0001562	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000076	PMID:26598328	PCS		1/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000010	OMIM:616854	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616854	Even-Plus syndrome		HP:0001047	OMIM:616854	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616854	Even-Plus syndrome		HP:0001263	PMID:26598328	PCS		1/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000470	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0011800	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0010575	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000668	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000007	PMID:26598328	PCS					I	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0003417	PMID:26598328	PCS		3/3			P	HPO:probinson[2017-06-22];HPO:probinson[2024-03-15]
OMIM:616854	Even-Plus syndrome		HP:0000664	PMID:26598328	PCS		3/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0001631	PMID:26598328	PCS		2/3			P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0000248	PMID:26598328	PCS		1/3			P	HPO:probinson[2017-06-22];HPO:probinson[2024-03-15]
OMIM:616854	Even-Plus syndrome		HP:0008428	PMID:26598328	PCS					P	HPO:probinson[2017-06-22]
OMIM:616854	Even-Plus syndrome		HP:0001655	PMID:26598328	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0001156	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0000276	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0001272	PMID:32220290	PCS		10/12			P	HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0001250	PMID:32220290	PCS		4/8			P	HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0003155	PMID:32220290	PCS		0/10			P	HPO:probinson[2020-06-17];HPO:probinson[2024-03-16]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0001263	PMID:32220290	PCS		12/12			P	HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0001251	PMID:32220290	PCS		5/12			P	HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0003593	PMID:32220290	PCS					C	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0001290	PMID:32220290	PCS		12/12			P	HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0003282	PMID:32220290	PCS		2/10			P	HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0041048	PMID:32220290	PCS					P	HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0009890	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0008593	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0011220	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0000007	PMID:32220290	TAS					I	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0000678	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0000219	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:618879	Neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures		HP:0005338	PMID:32220290	PCS					P	HPO:probinson[2020-06-17];HPO:probinson[2020-06-17]
OMIM:400042	Spermatogenic failure, Y-linked, 1		HP:0001450	PMID:19246359	PCS		1/1			I	HPO:probinson[2021-08-22]
OMIM:400042	Spermatogenic failure, Y-linked, 1		HP:0003251	PMID:19246359	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:400042	Spermatogenic failure, Y-linked, 1		HP:0011462	PMID:19246359	PCS		1/1			C	HPO:probinson[2022-08-03]
OMIM:400042	Spermatogenic failure, Y-linked, 1		HP:0012207	PMID:19246359	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:604288	Cardiomyopathy, dilated, 1H		HP:0003581	PMID:10486326	PCS					C	HPO:probinson[2022-07-04]
OMIM:604288	Cardiomyopathy, dilated, 1H		HP:0000006	PMID:10486326	PCS					I	HPO:probinson[2022-07-04]
OMIM:604288	Cardiomyopathy, dilated, 1H		HP:0001644	PMID:10486326	PCS					P	HPO:probinson[2022-07-04]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0009926	PMID:26749309	PCS	HP:0003577				P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0001089	OMIM:122000	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0007957	PMID:26749309	PCS	HP:0003593				P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0000585	PMID:26749309	PCS					P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0007915	PMID:26749309	PCS					P	HPO:probinson[2009-02-17]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0009918	OMIM:122000	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0011488	PMID:26749309	PCS					P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0031159	PMID:26749309	PCS		HP:0040283			P	HPO:probinson[2018-03-05]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0011490	PMID:26749309	PCS					P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0011483	PMID:26749309	PCS					P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0000613	PMID:26749309	PCS	HP:0003577				P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0025358	PMID:26749309	PCS					P	HPO:probinson[2017-06-14]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0000006	PMID:26749309	PCS					I	HPO:probinson[2009-02-17]
OMIM:122000	Corneal dystrophy, posterior polymorphous, 1		HP:0000501	PMID:26749309	PCS					P	HPO:probinson[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000286	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0003038	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0001970	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0004442	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0003071	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0012622	OMIM:218330	TAS					P	HPO:probinson[2014-01-18]
OMIM:218330	Cranioectodermal dysplasia		HP:0012623	PMID:20493458	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000639	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000954	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0001647	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0009466	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0001407	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0002217	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000674	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000556	PMID:20493458	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0001249	PMID:20493458	PCS		0/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0001382	PMID:22486404	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-03-14]
OMIM:218330	Cranioectodermal dysplasia		HP:0000293	OMIM:218330	IEA		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000691	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0001816	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000968	OMIM:218330	IEA					P	HPO:skoehler[2015-01-14]
OMIM:218330	Cranioectodermal dysplasia		HP:0000767	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000601	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0002705	OMIM:218330	TAS					P	HPO:skoehler[2015-12-30]
OMIM:218330	Cranioectodermal dysplasia		HP:0000007	PMID:22486404	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-03-14]
OMIM:218330	Cranioectodermal dysplasia		HP:0001538	PMID:20493458	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0002901	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000369	PMID:20493458	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000687	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0003774	PMID:20493458	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0030799	OMIM:218330	TAS					P	HPO:skoehler[2017-07-13]
OMIM:218330	Cranioectodermal dysplasia		HP:0003577	PMID:20493458	PCS		2/2			C	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0008905	PMID:20493458	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0001399	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000023	PMID:20493458	PCS		4/11			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0001156	PMID:20493458	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000463	OMIM:218330	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218330	Cranioectodermal dysplasia		HP:0001395	PMID:20493458	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0005792	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0002240	PMID:20493458	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0010306	PMID:20493458	PCS		11/11			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0032612	PMID:22486404	PCS		1/2			P	HPO:probinson[2020-03-14]
OMIM:218330	Cranioectodermal dysplasia		HP:0008070	PMID:20493458	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000939	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0009880	OMIM:218330	TAS					P	HPO:probinson[2012-06-10]
OMIM:218330	Cranioectodermal dysplasia		HP:0009882	OMIM:218330	TAS					P	HPO:probinson[2012-06-10]
OMIM:218330	Cranioectodermal dysplasia		HP:0006297	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000218	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0030084	OMIM:218330	TAS					P	HPO:skoehler[2015-12-30]
OMIM:218330	Cranioectodermal dysplasia		HP:0000411	PMID:20493458	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000774	PMID:20493458	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-03-14];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000773	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0005567	OMIM:218330	TAS					P	HPO:probinson[2014-01-18]
OMIM:218330	Cranioectodermal dysplasia		HP:0002213	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000431	PMID:20493458	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0000232	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000506	PMID:20493458	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0001837	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000668	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0006563	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000348	PMID:20493458	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0002205	PMID:20493458	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0002007	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000268	PMID:20493458	PCS		12/13			P	HPO:iea[2009-02-17];HPO:probinson[2020-03-14];HPO:probinson[2022-08-11];HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:218330	Cranioectodermal dysplasia		HP:0001799	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0000545	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:218330	Cranioectodermal dysplasia		HP:0001831	OMIM:218330	IEA					P	HPO:iea[2009-02-17]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0000089	PMID:19664745	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0005576	PMID:19664745	PCS	HP:0003621				P	HPO:probinson[2013-06-02];HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0001903	PMID:19664745	PCS	HP:0011463			HP:0012825	P	HPO:probinson[2013-06-02];HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0000097	PMID:19664745	PCS	HP:0003621				P	HPO:skoehler[2013-05-03];HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0004719	OMIM:613092	TAS					P	HPO:probinson[2013-06-02]
OMIM:613092	Hyperuricemic nephropathy, familial juvenile, 2		HP:0000093	PMID:19664745	PCS					P	HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0000092	PMID:19664745	PCS	HP:0003621			HP:0030650	P	HPO:probinson[2013-06-02];HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0000006	PMID:19664745	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0012622	PMID:19664745	PCS					P	HPO:probinson[2014-01-18];HPO:probinson[2022-04-05]
OMIM:613092	Tubulointerstitial kidney disease, autosomal dominant, 4		HP:0002149	PMID:19664745	PCS	HP:0011463				P	HPO:skoehler[2013-05-03];HPO:probinson[2022-04-05]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001770	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001377	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001476	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002980	PMID:12612583	PCS		11/18			P	HPO:probinson[2023-02-12]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0004322	PMID:12612583	PCS		5/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0010109	OMIM:311300	TAS					P	HPO:probinson[2012-06-08]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002164	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000160	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0003196	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001571	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001592	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0010047	OMIM:311300	TAS					P	HPO:probinson[2012-06-03]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0012368	OMIM:311300	TAS					P	HPO:skoehler[2013-10-22]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0005090	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0010055	OMIM:311300	TAS					P	HPO:probinson[2012-06-08]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0009882	OMIM:311300	TAS					P	HPO:probinson[2012-06-03]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002737	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000316	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0009642	OMIM:311300	TAS					P	HPO:probinson[2012-06-10]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001423	PMID:12612583	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000336	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001782	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000494	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000175	PMID:12612583	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000431	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002650	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0005048	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002673	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0004232	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001241	OMIM:311300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000272	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0003083	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0010041	OMIM:311300	TAS					P	HPO:probinson[2012-06-03]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0010044	OMIM:311300	TAS					P	HPO:probinson[2012-06-03]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002827	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0008089	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000767	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001539	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0008127	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0006389	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000405	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0001852	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0008404	OMIM:311300	TAS					P	HPO:skoehler[2013-05-03]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002007	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0009836	OMIM:311300	TAS					P	HPO:probinson[2012-06-03]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0000269	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:311300	Otopalatodigital syndrome, type I		HP:0002688	OMIM:311300	IEA					P	HPO:iea[2009-02-17]
OMIM:126500	Double nail for fifth toe		HP:0000924	OMIM:126500	IEA					P	HPO:iea[2009-02-17]
OMIM:126500	Double nail for fifth toe		HP:0000006	OMIM:126500	IEA					I	HPO:iea[2009-02-17]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000341	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000384	PMID:23315542;PMID:27007857	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0003577	PMID:35170830;PMID:23315542;PMID:27007857;PMID:23913798	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000040	PMID:23913798	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000160	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0001252	PMID:35170830	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0008070	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0011261	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0001508	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0012450	PMID:23913798	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0008897	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0002179	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0007628	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0002079	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0001140	PMID:23315542	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000293	PMID:27007857;PMID:23913798	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0011968	PMID:35170830;PMID:23913798	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0004451	PMID:23315542;PMID:27007857	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0030022	PMID:35170830;PMID:23315542;PMID:27007857;PMID:23913798	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0010536	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000506	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000729	PMID:23913798	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000007	PMID:23913798	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0001539	PMID:23315542;PMID:23913798	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0003319	PMID:23315542	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000664	PMID:27007857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000347	PMID:35170830;PMID:23315542;PMID:23913798	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0002643	PMID:23315542;PMID:23913798	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620458	Auriculocondylar syndrome 2B		HP:0000324	PMID:23315542	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0002751	PMID:35840571	PCS		4/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0000750	PMID:35840571	PCS		5/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0001344	PMID:35840571	PCS		1/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0001332	PMID:35840571	PCS		1/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0001250	PMID:35840571	PCS		3/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0011968	PMID:35840571	PCS		4/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0001263	PMID:35840571	PCS		8/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0003593	PMID:35840571	PCS					C	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0100021	PMID:35840571	PCS		1/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0410170	PMID:35840571	PCS		1/6			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0100035	PMID:35840571	PCS		1/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0033725	PMID:35840571	PCS		1/6			P	HPO:probinson[2023-07-07];HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0034295	PMID:35840571	PCS		3/6			P	HPO:probinson[2023-07-07];HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0007371	PMID:35840571	PCS		1/6			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0000729	PMID:35840571	PCS		4/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0000718	PMID:35840571	PCS		2/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0000739	PMID:35840571	PCS		7/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0000722	PMID:35840571	PCS		1/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0002119	PMID:35840571	PCS		1/6			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0002317	PMID:35840571	PCS		4/6			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0001417	PMID:35840571	PCS					I	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0000752	PMID:35840571	PCS		2/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0001257	PMID:35840571	PCS		2/8			P	HPO:probinson[2023-07-07]
OMIM:301107	Intellectual developmental disorder, X-linked 111		HP:0001249	PMID:35840571	PCS		8/8			P	HPO:probinson[2023-07-07]
OMIM:179010	Pyloric stenosis, infantile hypertrophic 1		HP:0002587	OMIM:179010	IEA					P	HPO:skoehler[2010-06-20]
OMIM:179010	Pyloric stenosis, infantile hypertrophic 1		HP:0001508	OMIM:179010	IEA					P	HPO:iea[2009-02-17]
OMIM:179010	Pyloric stenosis, infantile hypertrophic 1		HP:0002021	OMIM:179010	TAS					P	HPO:probinson[2009-02-17]
OMIM:179010	Pyloric stenosis, infantile hypertrophic 1		HP:0001426	OMIM:179010	IEA					I	HPO:iea[2009-02-17]
OMIM:179010	Pyloric stenosis, infantile hypertrophic 1		HP:0000006	OMIM:179010	IEA					I	HPO:iea[2009-02-17]
OMIM:179010	Pyloric stenosis, infantile hypertrophic 1		HP:0005977	OMIM:179010	TAS					P	HPO:probinson[2009-02-17]
OMIM:215600	Cirrhosis, familial		HP:0001254	OMIM:215600	IEA					P	HPO:iea[2009-02-17]
OMIM:215600	Cirrhosis, familial		HP:0004787	PMID:9011570	PCS		1/5			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:215600	Cirrhosis, familial		HP:0410069	PMID:3426740	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:215600	Cirrhosis, familial		HP:0001541	PMID:9011570	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:215600	Cirrhosis, familial		HP:0410067	PMID:2311216	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:215600	Cirrhosis, familial		HP:0003584	PMID:9011570	PCS		1/1			C	HPO:probinson[2022-08-28]
OMIM:215600	Cirrhosis, familial		HP:0001394	PMID:9011570	PCS		3/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:215600	Cirrhosis, familial		HP:0002040	PMID:9011570	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:215600	Cirrhosis, familial		HP:0002092	OMIM:215600	IEA					P	HPO:skoehler[2015-01-21]
OMIM:215600	Cirrhosis, familial		HP:0003270	OMIM:215600	IEA					P	HPO:iea[2009-02-17]
OMIM:215600	Cirrhosis, familial		HP:0000822	OMIM:215600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:215600	Cirrhosis, familial		HP:0000007	PMID:9011570	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-08-28]
OMIM:215600	Cirrhosis, familial		HP:0001945	OMIM:215600	IEA					P	HPO:iea[2009-02-17]
OMIM:215600	Cirrhosis, familial		HP:0002613	PMID:9011570	PCS		1/5			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:215600	Cirrhosis, familial		HP:0000952	OMIM:215600	IEA					P	HPO:iea[2009-02-17]
OMIM:215600	Cirrhosis, familial		HP:0001413	OMIM:215600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0003577	PMID:8789451	IEA		2/2			C	HPO:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0003198	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0001252	PMID:10449925	PCS		2/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0001290	PMID:8789451	PCS		2/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0012741	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0100750	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0011461	PMID:10449925	PCS		2/2			C	HPO:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000218	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0001522	PMID:8789451	PCS		2/2			C	HPO:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000278	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000033	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0001265	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0003687	PMID:8789451	PCS		2/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000054	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0001561	PMID:10449925	PCS	HP:0011461	2/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0003244	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0001382	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0002098	PMID:10449925;PMID:8789451	PCS		2/4			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0011968	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000807	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0001558	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000048	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0003811	PMID:10449925	IEA		2/2			C	HPO:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000047	PMID:8789451	PCS		2/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000883	PMID:8789451	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0008689	PMID:10449925	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:300219	Myotubular myopathy with abnormal genital development		HP:0000006	PMID:8789451	PCS					I	HPO:probinson[2021-10-22];HPO:probinson[2021-10-22]
OMIM:613086	Glaucoma 3, primary congenital, D		HP:0007957	OMIM:613086	TAS					P	HPO:probinson[2013-06-02]
OMIM:613086	Glaucoma 3, primary congenital, D		HP:0000613	OMIM:613086	TAS					P	HPO:probinson[2013-06-02]
OMIM:613086	Glaucoma 3, primary congenital, D		HP:0000007	OMIM:613086	TAS					I	HPO:probinson[2013-06-02]
OMIM:613086	Glaucoma 3, primary congenital, D		HP:0001083	OMIM:613086	TAS		1/8			P	HPO:probinson[2013-06-02]
OMIM:613086	Glaucoma 3, primary congenital, D		HP:0008007	OMIM:613086	TAS					P	HPO:probinson[2013-06-02]
OMIM:614931	Ectodermal dysplasia 9, hair/nail type		HP:0002223	PMID:28403827	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000561	PMID:28403827;PMID:23063621	PCS		4/4			P	HPO:probinson[2019-07-14];HPO:probinson[2024-03-15];ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000164	PMID:28403827;PMID:23063621	PCS		0/6			P	HPO:probinson[2019-07-14];HPO:probinson[2024-03-15];ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, hair/nail type		HP:0003577	PMID:28403827;PMID:23063621	PCS		6/6			C	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, hair/nail type		HP:0001792	PMID:23063621	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0002298	PMID:23315978	PCS	HP:0003577	1/1			P	HPO:probinson[2019-07-14]
OMIM:614931	Ectodermal dysplasia 9, hair/nail type		HP:0000023	PMID:28403827;PMID:23063621	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0032226	PMID:23063621	PCS		0/3			P	HPO:probinson[2019-07-14];HPO:probinson[2024-03-15]
OMIM:614931	Ectodermal dysplasia 9, hair/nail type		HP:0012741	PMID:28403827;PMID:23063621	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0008070	OMIM:614931	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614931	Ectodermal dysplasia 9, hair/nail type		HP:0040039	PMID:28403827;PMID:23063621	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0500262	PMID:28403827;PMID:23063621	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-15];ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000924	PMID:23063621	PCS		0/3			P	HPO:probinson[2019-07-14];HPO:probinson[2024-03-15]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000968	PMID:23063621	PCS		3/3			P	HPO:skoehler[2015-01-14];HPO:probinson[2019-07-14];HPO:probinson[2024-03-15]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000707	PMID:23063621	PCS		0/3			P	HPO:probinson[2019-07-14];HPO:probinson[2024-03-15]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000007	PMID:23063621	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2019-07-14]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0008404	PMID:23063621	PCS		3/3			P	HPO:skoehler[2013-05-03];HPO:probinson[2019-07-14];HPO:probinson[2024-03-15]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0008404	PMID:23315978	PCS	HP:0003577	1/1			P	HPO:probinson[2019-07-14]
OMIM:614931	Ectodermal dysplasia 9, hair/nail type		HP:0008404	PMID:28403827	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000971	PMID:23063621	PCS		0/3			P	HPO:probinson[2019-07-14];HPO:probinson[2024-03-15]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0001598	PMID:23315978	TAS					P	HPO:skoehler[2012-11-20];HPO:probinson[2019-07-14]
OMIM:614931	Ectodermal dysplasia 9, Hair/nail type		HP:0000478	PMID:23063621	IEA		0/3			P	HPO:probinson[2019-07-14];HPO:probinson[2024-03-15]
OMIM:258700	Opticocochleodentate degeneration		HP:0000572	OMIM:258700	IEA					P	HPO:iea[2009-02-17]
OMIM:258700	Opticocochleodentate degeneration		HP:0002510	OMIM:258700	IEA					P	HPO:iea[2009-02-17]
OMIM:258700	Opticocochleodentate degeneration		HP:0000365	OMIM:258700	IEA					P	HPO:iea[2009-02-17]
OMIM:258700	Opticocochleodentate degeneration		HP:0001344	OMIM:258700	IEA					P	HPO:iea[2009-02-17]
OMIM:258700	Opticocochleodentate degeneration		HP:0005102	OMIM:258700	IEA					P	HPO:iea[2009-02-17]
OMIM:258700	Opticocochleodentate degeneration		HP:0000007	OMIM:258700	IEA					I	HPO:iea[2009-02-17]
OMIM:258700	Opticocochleodentate degeneration		HP:0000648	OMIM:258700	IEA					P	HPO:iea[2009-02-17]
OMIM:258700	Opticocochleodentate degeneration		HP:0001268	OMIM:258700	IEA					P	HPO:iea[2009-02-17]
OMIM:613938	Parasomnia, Sleepwalking type		HP:0030765	OMIM:613938	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613938	Parasomnia, Sleepwalking type		HP:0000006	OMIM:613938	TAS					I	HPO:skoehler[2012-10-17]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0002322	PMID:26942284	PCS		3/3			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0003676	PMID:26942284	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0031825	PMID:26942284	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0003596	PMID:26942284	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0002120	PMID:26942284	PCS		1/3			P	HPO:skoehler[2017-07-13]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0002063	PMID:26942284	PCS		3/3			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0000020	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0002185	PMID:26942284	PCS		1/1			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0001350	PMID:26942284	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0012332	PMID:26942284	PCS		2/3			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0000716	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0000738	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0011462	PMID:26942284	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0001268	PMID:26942284	PCS		3/3			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0001347	PMID:26942284	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0002015	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0001289	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0002451	PMID:26942284	PCS		2/3			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0002172	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0100315	PMID:26942284	PCS		1/1			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0000726	PMID:26942284	PCS		3/3			P	HPO:skoehler[2017-07-13]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0007256	PMID:26942284	PCS		1/3			P	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0000007	PMID:26942284	PCS					I	HPO:probinson[2017-06-20]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0002529	PMID:26942284	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0002548	PMID:26942284	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0002527	PMID:26942284	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0002505	PMID:26942284	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0002304	PMID:26942284	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0000741	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:616840	Parkinson disease 23, autosomal recessive early-onset		HP:0001257	PMID:26942284	PCS		1/3			P	HPO:skoehler[2017-07-13]
OMIM:616840	Parkinson disease 23, autosomal recessive, early onset		HP:0004326	PMID:26942284	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:243320	Intrinsic factor and R binder, combined congenital deficiency of		HP:0000707	OMIM:243320	IEA					P	HPO:iea[2009-02-17]
OMIM:243320	Intrinsic factor and R binder, combined congenital deficiency of		HP:0001939	OMIM:243320	IEA					P	HPO:iea[2009-02-17]
OMIM:243320	Intrinsic factor and R binder, combined congenital deficiency of		HP:0001889	OMIM:243320	IEA					P	HPO:iea[2009-02-17]
OMIM:243320	Intrinsic factor and R binder, combined congenital deficiency of		HP:0000007	OMIM:243320	IEA					I	HPO:iea[2009-02-17]
OMIM:243320	Intrinsic factor and R binder, combined congenital deficiency of		HP:0001510	OMIM:243320	IEA					P	HPO:iea[2009-02-17]
OMIM:243320	Intrinsic factor and R binder, combined congenital deficiency of		HP:0005219	OMIM:243320	IEA					P	HPO:iea[2009-02-17]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0002037	PMID:26358773	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0001561	PMID:26358773	PCS		7/7			P	HPO:probinson[2017-06-20]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0030674	PMID:26358773	PCS		7/7			C	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0033994	PMID:26358773	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0032024	PMID:26358773	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0032487	PMID:26358773	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0003270	PMID:26358773	PCS		7/7			P	HPO:probinson[2017-06-20]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0032489	PMID:26358773	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0010931	PMID:26358773	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0034470	PMID:26358773	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0032484	PMID:26358773	PCS		6/7			P	HPO:probinson[2019-09-07]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0011473	PMID:26358773	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0000007	PMID:26358773	PCS					I	HPO:probinson[2017-06-20]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0008897	PMID:26358773	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:616868	Diarrhea 8, secretory sodium, congenital		HP:0005208	PMID:26358773	PCS	HP:0003577	7/7			P	HPO:probinson[2017-06-20]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0003026	PMID:31883644	PCS					P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0003422	PMID:31883644	PCS					P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0010958	PMID:31883644	PCS		1/5			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0001762	PMID:31883644	PCS		1/5			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0011638	PMID:31883644	PCS		1/3			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0000122	PMID:31883644	PCS		1/5			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0004383	PMID:31883644	IEA		1/3			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0010306	PMID:31883644	PCS					P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0001719	PMID:31883644	PCS		1/3			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0002948	PMID:31883644	PCS					P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0001647	PMID:31883644	PCS		1/3			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0000007	PMID:31883644	PCS					I	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0001643	PMID:31883644	PCS		1/3			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0001522	PMID:31883644	PCS					C	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0000960	PMID:31883644	PCS		2/5			P	HPO:probinson[2020-07-15]
OMIM:618845	Vertebral, cardiac, renal, and limb defects syndrome 3		HP:0005999	PMID:31883644	PCS		1/5		HP:0012833	P	HPO:probinson[2020-07-15]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0003235	PMID:11281457	PCS		3/3			P	HPO:probinson[2012-07-16];HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0003233	OMIM:605814	TAS					P	HPO:probinson[2012-07-16]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0003354	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0003231	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0003155	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0001394	OMIM:605814	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0002161	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0012202	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0031964	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0001508	OMIM:605814	TAS					P	HPO:probinson[2012-07-16]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0001406	OMIM:605814	TAS					P	HPO:probinson[2012-07-16]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0001403	PMID:11281457	PCS		1/1			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0003623	PMID:11281457	PCS		3/3			C	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0031956	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0002155	OMIM:605814	TAS					P	HPO:probinson[2012-07-16]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0003124	OMIM:605814	TAS					P	HPO:probinson[2012-07-16]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0011966	PMID:11281457	PCS		3/3			P	HPO:probinson[2012-07-18];HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0030948	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0002908	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0500153	PMID:11281457	PCS		3/3			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0006580	PMID:11281457	PCS		1/1			P	HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0002904	PMID:11281457	PCS		3/3			P	HPO:probinson[2012-07-16];HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0000007	PMID:11281457	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-03-11]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0001510	OMIM:605814	TAS					P	HPO:probinson[2012-07-16]
OMIM:605814	Citrullinemia, type II, neonatal-onset		HP:0001414	PMID:11281457	PCS		1/1			P	HPO:probinson[2023-03-11]
OMIM:314250	Dystonia 3, torsion, X-linked		HP:0001419	OMIM:314250	TAS					I	HPO:probinson[2009-02-17]
OMIM:314250	Dystonia 3, torsion, X-linked		HP:0003581	OMIM:314250	TAS					C	HPO:probinson[2012-07-19]
OMIM:314250	Dystonia 3, torsion, X-linked		HP:0002072	OMIM:314250	TAS					P	HPO:probinson[2009-02-17]
OMIM:314250	Dystonia 3, torsion, X-linked		HP:0002548	OMIM:314250	TAS					P	HPO:probinson[2009-02-17]
OMIM:314250	Dystonia 3, torsion, X-linked		HP:0001304	OMIM:314250	TAS					P	HPO:probinson[2009-02-17]
OMIM:314250	Dystonia 3, torsion, X-linked		HP:0001337	OMIM:314250	TAS					P	HPO:skoehler[2010-06-20]
OMIM:314250	Dystonia 3, torsion, X-linked		HP:0001336	OMIM:314250	TAS					P	HPO:probinson[2009-02-17]
OMIM:154800	Mastocytosis, cutaneous		HP:0001034	OMIM:154800	TAS					P	HPO:probinson[2009-02-17]
OMIM:154800	Mastocytosis, cutaneous		HP:0001025	OMIM:154800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:154800	Mastocytosis, cutaneous		HP:0000969	OMIM:154800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:154800	Mastocytosis, cutaneous		HP:0007583	OMIM:154800	IEA					P	HPO:iea[2009-02-17]
OMIM:154800	Mastocytosis, cutaneous		HP:0010783	OMIM:154800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:154800	Mastocytosis, cutaneous		HP:0000006	OMIM:154800	IEA					I	HPO:iea[2009-02-17]
OMIM:154800	Mastocytosis, cutaneous		HP:0200151	OMIM:154800	TAS					P	HPO:skoehler[2013-06-16]
OMIM:103780	Alcohol dependence		HP:0001426	OMIM:103780	TAS					I	HPO:probinson[2020-06-27]
OMIM:103780	Alcohol dependence		HP:0030955	OMIM:103780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000286	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0010529	PMID:8957962	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000486	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000365	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0002020	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0010049	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000518	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0009102	PMID:16953888	PCS	HP:0003621				P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000718	PMID:11869383	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000717	PMID:18564888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000316	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000954	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0003745	ISBN-13:978-0721606156	PCS					I	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0002216	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000752	PMID:16953888;PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000311	PMID:16953888;ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001763	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001840	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001249	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001540	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0002795	PMID:20038906	PCS	HP:0003623				P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000252	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000494	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0100024	PMID:8957962	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0100025	PMID:8957962	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000648	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000202	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000047	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000322	PMID:16953888	PCS	HP:0003621				P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000369	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000402	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000324	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001276	PMID:20038906	PCS	HP:0003621				P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000384	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000023	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0010865	PMID:8957962	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0010743	PMID:16953888	PCS	HP:0003621				P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000739	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0030680	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0008872	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000733	PMID:11869383	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0200046	PMID:1695388	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000736	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0002714	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000218	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000377	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000179	PMID:16953888	PCS	HP:0003621				P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000336	PMID:16953888	PCS	HP:0003621				P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000077	PMID:16953888;PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000275	PMID:16953888	PCS	HP:0003621				P	HPO:iea[2012-05-01]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000431	PMID:1695388	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0002650	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000750	PMID:10355811	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001288	PMID:8957962	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000276	PMID:16953888	PCS	HP:0003621				P	HPO:iea[2012-05-01]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000193	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000273	PMID:8957962	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001042	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000470	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001518	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000308	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0010780	PMID:20038906	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001319	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001159	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0001510	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000028	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000545	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0005437	PMID:16953888	PCS					P	HPO:iea[2012-04-24]
OMIM:123450	Cri-Du-Chat syndrome		HP:0000742	PMID:8957962	PCS					P	HPO:iea[2012-04-24]
OMIM:119900	Digital clubbing, isolated congenital		HP:0003577	PMID:18805827	PCS					C	HPO:probinson[2022-03-15]
OMIM:119900	Digital clubbing, isolated congenital		HP:0001217	PMID:18805827	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-07-17]
OMIM:119900	Digital clubbing, isolated congenital		HP:0000007	PMID:18805827	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-17]
OMIM:620470	Congenital smooth muscle hamartoma with or without hemihypertrophy		HP:0001442	PMID:32170967	PCS		1/1			I	HPO:probinson[2024-03-10]
OMIM:620470	Congenital smooth muscle hamartoma with or without hemihypertrophy		HP:0003593	PMID:32170967	PCS		1/1			C	HPO:probinson[2024-03-10]
OMIM:620470	Congenital smooth muscle hamartoma with or without hemihypertrophy		HP:0000998	PMID:32170967	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620470	Congenital smooth muscle hamartoma with or without hemihypertrophy		HP:0010566	PMID:32170967	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620470	Congenital smooth muscle hamartoma with or without hemihypertrophy		HP:0001528	PMID:32170967	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:611875	Brugada syndrome 3		HP:0012232	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:611875	Brugada syndrome 3		HP:0012272	PMID:17224476	PCS					P	HPO:probinson[2013-04-07]
OMIM:611875	Brugada syndrome 3		HP:0005110	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:611875	Brugada syndrome 3		HP:0004308	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:611875	Brugada syndrome 3		HP:0001279	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:611875	Brugada syndrome 3		HP:0000006	PMID:17224476	PCS					I	HPO:probinson[2013-04-03]
OMIM:611875	Brugada syndrome 3		HP:0001645	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0002521	PMID:36283405	PCS		2/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0000483	PMID:36283405	PCS		1/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0000540	PMID:36283405	PCS		1/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001250	PMID:36283405	PCS	HP:0003593	6/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0002263	PMID:36283405	PCS		6/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001252	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001274	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0025102	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0003593	PMID:36283405	PCS		7/7			C	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0100704	PMID:36283405	PCS		6/6			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0000218	PMID:36283405	PCS		4/5			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0030084	PMID:36283405	PCS		2/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001302	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001347	PMID:36283405	PCS		6/6			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0000431	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0005445	PMID:36283405	PCS		2/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0002650	PMID:36283405	PCS		1/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0003487	PMID:36283405	PCS		2/3			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001321	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0011968	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0005487	PMID:36283405	PCS		5/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001263	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0010851	PMID:36283405	PCS		1/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0100541	PMID:36283405	PCS		1/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0003819	PMID:36283405	PCS		1/7			C	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0002509	PMID:36283405	PCS		5/6			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0001339	PMID:36283405	PCS		7/7			P	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0000007	PMID:36283405	PCS					I	HPO:probinson[2023-07-11]
OMIM:620316	Cortical dysplasia, complex, with other brain malformations 12		HP:0000028	PMID:36283405	PCS		2/5	MALE		P	HPO:probinson[2023-07-11];HPO:probinson[2023-07-11]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0002587	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0003236	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0002188	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0011924	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0008807	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0002151	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0002020	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0011923	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0001518	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0000007	PMID:30452684	PCS					I	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0008872	PMID:30452684	PCS	HP:0003593	1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0001319	PMID:30452684	PCS	HP:0003623	1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0008347	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618851	Combined oxidative phosphorylation deficiency 43		HP:0001511	PMID:30452684	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:138070	GLUCOGLYCINURIA		HP:0003076	OMIM:138070	IEA					P	HPO:skoehler[2010-06-20]
OMIM:138070	GLUCOGLYCINURIA		HP:0003108	OMIM:138070	IEA					P	HPO:iea[2009-02-17]
OMIM:138070	GLUCOGLYCINURIA		HP:0000006	OMIM:138070	IEA					I	HPO:iea[2009-02-17]
OMIM:204730	Amino aciduria with mental deficiency, dwarfism, muscular dystrophy,osteoporosis, and acidosis		HP:0003510	OMIM:204730	IEA					P	HPO:iea[2009-02-17]
OMIM:204730	Amino aciduria with mental deficiency, dwarfism, muscular dystrophy,osteoporosis, and acidosis		HP:0000939	OMIM:204730	IEA					P	HPO:iea[2009-02-17]
OMIM:204730	Amino aciduria with mental deficiency, dwarfism, muscular dystrophy,osteoporosis, and acidosis		HP:0003355	OMIM:204730	IEA					P	HPO:iea[2009-02-17]
OMIM:204730	Amino aciduria with mental deficiency, dwarfism, muscular dystrophy,osteoporosis, and acidosis		HP:0003560	OMIM:204730	IEA					P	HPO:iea[2009-02-17]
OMIM:204730	Amino aciduria with mental deficiency, dwarfism, muscular dystrophy,osteoporosis, and acidosis		HP:0000007	OMIM:204730	IEA					I	HPO:iea[2009-02-17]
OMIM:204730	Amino aciduria with mental deficiency, dwarfism, muscular dystrophy,osteoporosis, and acidosis		HP:0001249	OMIM:204730	TAS					P	HPO:skoehler[2009-02-17]
OMIM:204730	Amino aciduria with mental deficiency, dwarfism, muscular dystrophy,osteoporosis, and acidosis		HP:0001941	OMIM:204730	IEA					P	HPO:iea[2009-02-17]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0001399	OMIM:177000	IEA					P	HPO:iea[2009-02-17]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0002155	OMIM:177000	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0000969	OMIM:177000	IEA					P	HPO:iea[2009-02-17]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0011463	OMIM:177000	TAS				HP:0012825	C	HPO:probinson[2012-05-05]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:6000697	PMID:8571955	PCS					P	HPO:probinson[2024-05-09]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0001878	OMIM:177000	IEA					P	HPO:iea[2009-02-17]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0001081	OMIM:177000	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0000007	OMIM:177000	IEA					I	HPO:iea[2009-02-17]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0000964	OMIM:177000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0000989	OMIM:177000	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:177000	Protoporphyria, erythropoietic, 1		HP:0010783	OMIM:177000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:256710	Elejalde disease		HP:0001250	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0002220	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001010	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001252	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001263	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001251	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0003593	OMIM:256710	IEA					C	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001290	OMIM:256710	TAS					P	HPO:skoehler[2017-07-13]
OMIM:256710	Elejalde disease		HP:0000639	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0003819	OMIM:256710	IEA					C	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0000007	OMIM:256710	IEA					I	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001008	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0002218	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001257	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0001249	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:256710	Elejalde disease		HP:0000577	OMIM:256710	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0001760	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0007715	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000431	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000574	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0004322	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0004661	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000581	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0025586	OMIM:210745	IEA					P	HPO:skoehler[2018-10-08]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0010554	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000508	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000007	OMIM:210745	IEA					I	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000458	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000565	OMIM:210745	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000664	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000179	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:210745	Blepharophimosis with ptosis, syndactyly, and short stature		HP:0000303	OMIM:210745	IEA					P	HPO:iea[2009-02-17]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0010913	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0000007	PMID:25653144	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0002922	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0031993	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0002315	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0010911	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0010910	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0031964	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618850	Hypervalinemia or hyperleucine-isoleucinemia		HP:0001348	PMID:25653144	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:309200	Major affective disorder 2		HP:0003593	OMIM:309200	IEA					C	HPO:iea[2009-02-17]
OMIM:309200	Major affective disorder 2		HP:0007302	OMIM:309200	IEA					P	HPO:iea[2009-02-17]
OMIM:309200	Major affective disorder 2		HP:0001423	OMIM:309200	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0002421	PMID:31587869	PCS	HP:0003593	2/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0002188	PMID:31587869	PCS		4/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0031936	PMID:31587869	PCS		4/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0003487	PMID:31587869	PCS		1/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0001310	PMID:31587869	PCS		1/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0001251	PMID:31587869	PCS		2/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0001290	PMID:31587869	PCS		1/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0002080	PMID:31587869	PCS		1/4			P	HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0012043	PMID:31587869	PCS	HP:0003623	4/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0001328	PMID:31587869	PCS		1/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0000648	PMID:31587869	PCS		1/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0002415	PMID:31587869	PCS					P	HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0000047	PMID:31587869	PCS		1/3	MALE		P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0000006	PMID:31587869	PCS					I	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0000545	PMID:31587869	PCS		3/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618688	Leukodystrophy, hypomyelinating, 19, transient infantile		HP:0002599	PMID:31587869	PCS		2/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0002069	PMID:34585293	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0003577	PMID:34585293	PCS		1/1			C	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0006989	PMID:35790048	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000340	PMID:35790048	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0002188	PMID:34585293	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0002540	PMID:34585293	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0001250	PMID:35790048	PCS		0/4			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0001252	PMID:35790048	PCS		2/4			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0001251	PMID:35790048	PCS		1/4			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0003593	PMID:35790048	PCS		4/4			C	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000637	PMID:35790048	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0002317	PMID:35790048	PCS		1/4			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0001249	PMID:35790048	PCS		4/4			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0009748	PMID:35790048	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0001344	PMID:34585293	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000750	PMID:35790048	PCS		4/4			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0002352	PMID:35790048	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0001263	PMID:34585293;PMID:35790048	PCS		5/5			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0005484	PMID:34585293	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0034295	PMID:35790048	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000729	PMID:35790048	PCS		2/4			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0030890	PMID:35790048	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000426	PMID:35790048	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000448	PMID:35790048	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000007	PMID:34585293	PCS					I	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0000664	PMID:35790048	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620317	Neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities		HP:0001257	PMID:35790048	PCS		0/4			P	HPO:probinson[2023-07-09]
OMIM:619582	Joubert syndrome 40		HP:0100259	PMID:33531668;PMID:34539760	PCS		5/5			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0000609	PMID:33531668	PCS		2/4			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0003577	PMID:34539760	PCS		1/1			C	HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0001263	PMID:33531668;PMID:34539760	PCS		5/5			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0001252	PMID:33531668;PMID:34539760	PCS		5/5			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0000657	PMID:33531668	PCS		3/4			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0000007	PMID:33531668	PCS					I	HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0002419	PMID:33531668;PMID:34539760	PCS		5/5			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0001270	PMID:34539760	PCS		1/1			P	HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0007874	PMID:34539760	PCS		1/1			P	HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0005280	PMID:34539760	PCS		1/1			P	HPO:probinson[2021-12-18]
OMIM:619582	Joubert syndrome 40		HP:0001249	PMID:33531668	PCS		4/4			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0010627	PMID:28402530	PCS		4/5			P	HPO:probinson[2023-07-18]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0000486	PMID:28402530	PCS		3/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0010626	PMID:28402530	PCS		1/5			P	HPO:probinson[2023-07-18]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0000540	PMID:28402530	PCS		2/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0004322	PMID:28402530	PCS		5/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0030344	PMID:28402530	PCS		1/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0030353	PMID:28402530	PCS		5/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0030341	PMID:28402530	PCS		1/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0011755	PMID:28402530	PCS		1/5			P	HPO:probinson[2023-07-18]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0034323	PMID:28402530	PCS		5/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0034976	PMID:28402530	PCS		2/5			P	HPO:probinson[2023-07-18]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0034978	PMID:28402530	PCS		3/5			P	HPO:probinson[2023-07-18]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0031098	PMID:28402530	PCS		2/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0000508	PMID:28402530	PCS		1/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0002920	PMID:28402530	PCS		1/5			P	HPO:probinson[2023-07-13]
OMIM:620303	Pituitary hormone deficiency, combined or isolated, 8		HP:0000006	PMID:28402530	PCS					I	HPO:probinson[2023-07-13]
OMIM:304730	Dermoids of cornea		HP:0007957	OMIM:304730	TAS					P	HPO:skoehler[2015-01-21]
OMIM:304730	Dermoids of cornea		HP:0001417	OMIM:304730	IEA					I	HPO:iea[2009-02-17]
OMIM:304730	Dermoids of cornea		HP:0000478	OMIM:304730	IEA					P	HPO:iea[2009-02-17]
OMIM:240600	Glycogen storage disease 0, liver		HP:0001250	OMIM:240600	IEA					P	HPO:iea[2009-02-17]
OMIM:240600	Glycogen storage disease 0, liver		HP:0002151	OMIM:240600	TAS					P	HPO:probinson[2009-02-17]
OMIM:240600	Glycogen storage disease 0, liver		HP:0000007	OMIM:240600	IEA					I	HPO:iea[2009-02-17]
OMIM:240600	Glycogen storage disease 0, liver		HP:0001998	OMIM:240600	IEA					P	HPO:iea[2009-02-17]
OMIM:240600	Glycogen storage disease 0, liver		HP:0011998	OMIM:240600	TAS					P	HPO:probinson[2009-02-17]
OMIM:240600	Glycogen storage disease 0, liver		HP:0003162	OMIM:240600	IEA					P	HPO:iea[2009-02-17]
OMIM:240600	Glycogen storage disease 0, liver		HP:0001946	OMIM:240600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0008749	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001671	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000463	OMIM:217980	IEA					P	HPO:skoehler[2010-06-18]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001156	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000260	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000581	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001252	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001274	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0003196	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0012745	OMIM:217980	TAS					P	HPO:skoehler[2014-03-24]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0100790	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001290	OMIM:217980	TAS					P	HPO:skoehler[2017-07-13]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000316	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0030680	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0002779	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0009623	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0002714	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0030084	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001643	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000774	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0002777	OMIM:217980	TAS	HP:0003577				P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000377	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0005989	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001249	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001600	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001545	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000252	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000175	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0004279	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001321	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000293	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0002098	OMIM:217980	TAS	HP:0003623				P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000470	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0005280	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000506	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000508	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000007	OMIM:217980	IEA					I	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001638	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0001159	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000201	OMIM:217980	IEA					P	HPO:iea[2009-02-17]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000047	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000028	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0000347	OMIM:217980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:217980	Corpus callosum, agenesis of, with facial anomalies and Robin sequence		HP:0002643	OMIM:217980	TAS					P	HPO:skoehler[2017-07-13]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0002069	PMID:36074901	PCS		13/13			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0003621	PMID:36074901	PCS		2/18			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0000750	PMID:36074901	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0001344	PMID:36074901	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0002376	PMID:36074901	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0002373	PMID:36074901	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0002384	PMID:36074901	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0002121	PMID:36074901	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0010819	PMID:36074901	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0001263	PMID:36074901	PCS		21/23			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0003593	PMID:36074901	PCS		8/18			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0032794	PMID:36074901	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0012469	PMID:36074901	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0011463	PMID:36074901	PCS		8/18			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0032792	PMID:36074901	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0031165	PMID:36074901	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0007334	PMID:36074901	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0007359	PMID:36074901	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0001249	PMID:36074901	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620465	Epilepsy, early-onset, 3, with or without developmental delay		HP:0000006	PMID:36074901	PCS					I	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:244300	Kapur-Toriello syndrome		HP:0000384	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0001250	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000480	PMID:20358618	PCS					P	HPO:probinson[2017-12-13]
OMIM:244300	Kapur-Toriello syndrome		HP:0100490	OMIM:244300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0002162	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000518	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0001629	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000954	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000414	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000612	PMID:1776630	PCS					P	HPO:probinson[2017-12-13]
OMIM:244300	Kapur-Toriello syndrome		HP:0009765	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000059	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0001302	OMIM:244300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:244300	Kapur-Toriello syndrome		HP:0001643	OMIM:244300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:244300	Kapur-Toriello syndrome		HP:0002019	OMIM:244300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:244300	Kapur-Toriello syndrome		HP:0001864	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000175	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000054	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000079	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0002650	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000470	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0010557	OMIM:244300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:244300	Kapur-Toriello syndrome		HP:0009473	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000007	OMIM:244300	IEA					I	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000568	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0007598	OMIM:244300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000405	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0001511	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0001631	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0009778	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000204	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000028	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0002566	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0000369	OMIM:244300	IEA					P	HPO:iea[2009-02-17]
OMIM:244300	Kapur-Toriello syndrome		HP:0002126	OMIM:244300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:119915	Cluster headache, familial		HP:0012199	OMIM:119915	TAS					P	HPO:probinson[2013-03-12]
OMIM:119915	Cluster headache, familial		HP:0031417	OMIM:119915	IEA					P	HPO:skoehler[2018-10-08]
OMIM:119915	Cluster headache, familial		HP:0012531	OMIM:119915	TAS					P	HPO:skoehler[2015-12-30]
OMIM:119915	Cluster headache, familial		HP:0000969	OMIM:119915	IEA					P	HPO:skoehler[2010-06-20]
OMIM:119915	Cluster headache, familial		HP:0000616	OMIM:119915	IEA					P	HPO:skoehler[2012-11-16]
OMIM:119915	Cluster headache, familial		HP:0000508	OMIM:119915	IEA					P	HPO:skoehler[2012-11-16]
OMIM:119915	Cluster headache, familial		HP:0000975	OMIM:119915	IEA					P	HPO:skoehler[2012-11-16]
OMIM:119915	Cluster headache, familial		HP:0000713	OMIM:119915	IEA					P	HPO:iea[2009-02-17]
OMIM:119915	Cluster headache, familial		HP:0000006	OMIM:119915	IEA					I	HPO:iea[2009-02-17]
OMIM:202355	Adrenocortical unresponsiveness to acth with postreceptor defect		HP:0003154	OMIM:202355	IEA					P	HPO:iea[2009-02-17]
OMIM:202355	Adrenocortical unresponsiveness to acth with postreceptor defect		HP:0000007	OMIM:202355	IEA					I	HPO:iea[2009-02-17]
OMIM:202355	Adrenocortical unresponsiveness to acth with postreceptor defect		HP:0000953	OMIM:202355	IEA					P	HPO:iea[2009-02-17]
OMIM:189490	Tooth malformation		HP:0000692	OMIM:189490	IEA					P	HPO:iea[2009-02-17]
OMIM:189490	Tooth malformation		HP:0003828	OMIM:189490	IEA					M	HPO:skoehler[2010-06-19]
OMIM:189490	Tooth malformation		HP:0003829	OMIM:189490	IEA					I	HPO:skoehler[2010-06-19]
OMIM:189490	Tooth malformation		HP:0000668	OMIM:189490	IEA					P	HPO:iea[2009-02-17]
OMIM:189490	Tooth malformation		HP:0000006	OMIM:189490	IEA					I	HPO:iea[2009-02-17]
OMIM:613087	Atrial septal defect 6		HP:0003577	PMID:18830233	PCS		3/3			C	HPO:probinson[2023-02-10]
OMIM:613087	Atrial septal defect 6		HP:0001662	OMIM:613087	TAS		HP:0040283			P	HPO:skoehler[2013-06-03]
OMIM:613087	Atrial septal defect 6		HP:0005110	OMIM:613087	TAS		HP:0040283			P	HPO:skoehler[2013-06-03]
OMIM:613087	Atrial septal defect 6		HP:0001631	OMIM:613087	TAS	HP:0003577	3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-10]
OMIM:613087	Atrial septal defect 6		HP:0000006	PMID:18830233	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2023-02-10]
OMIM:300218	Syndromic X-linked intellectual disability 7		HP:0001249	OMIM:300218	IEA					P	HPO:skoehler[2015-01-27]
OMIM:301106	Spermatogenic failure, X-linked, 7		HP:0034309	PMID:36481789	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:301106	Spermatogenic failure, X-linked, 7		HP:0003251	PMID:36481789	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:301106	Spermatogenic failure, X-linked, 7		HP:0011462	PMID:36481789	PCS		2/2			C	HPO:probinson[2023-06-18]
OMIM:301106	Spermatogenic failure, X-linked, 7		HP:0034795	PMID:36481789	PCS		2/2			P	HPO:probinson[2023-07-18]
OMIM:301106	Spermatogenic failure, X-linked, 7		HP:0012207	PMID:36481789	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:301106	Spermatogenic failure, X-linked, 7		HP:0001417	PMID:36481789	PCS					I	HPO:probinson[2023-06-18]
OMIM:301106	Spermatogenic failure, X-linked, 7		HP:0012205	PMID:36481789	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:248260	Magnesium, elevated red cell		HP:0001939	OMIM:248260	IEA					P	HPO:iea[2009-02-17]
OMIM:248260	Magnesium, elevated red cell		HP:0000007	OMIM:248260	IEA					I	HPO:iea[2009-02-17]
OMIM:400043	DEAFNESS, Y-LINKED 1		HP:0000407	OMIM:400043	IEA					P	HPO:skoehler[2010-06-20]
OMIM:400043	DEAFNESS, Y-LINKED 1		HP:0001450	OMIM:400003	IEA					I	HPO:skoehler[2010-06-20]
OMIM:400043	DEAFNESS, Y-LINKED 1		HP:0000360	OMIM:400043	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:176450	Currarino syndrome		HP:0002025	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0000143	PMID:10749657	PCS			FEMALE		P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-12]
OMIM:176450	Currarino syndrome		HP:0003577	PMID:10749657	PCS		22/22			C	HPO:probinson[2022-08-12]
OMIM:176450	Currarino syndrome		HP:0002023	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0002144	PMID:10749657	PCS		4/22			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-12]
OMIM:176450	Currarino syndrome		HP:0001153	OMIM:176450	TAS			FEMALE		P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0000020	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0000085	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0003270	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0010305	PMID:10749657	PCS		1/22			P	HPO:probinson[2022-08-12]
OMIM:176450	Currarino syndrome		HP:0010447	OMIM:176450	TAS					P	HPO:skoehler[2010-06-18]
OMIM:176450	Currarino syndrome		HP:0012450	OMIM:176450	TAS					P	HPO:skoehler[2013-11-28]
OMIM:176450	Currarino syndrome		HP:0003829	OMIM:176450	TAS					I	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0100806	OMIM:176450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:176450	Currarino syndrome		HP:0002617	OMIM:176450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:176450	Currarino syndrome		HP:0000813	OMIM:176450	TAS			FEMALE		P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0009789	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0000011	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0000010	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0000076	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0004796	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0001263	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0007293	OMIM:176450	TAS					P	HPO:probinson[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0009791	OMIM:176450	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-12]
OMIM:176450	Currarino syndrome		HP:0009790	PMID:9843207	PCS	HP:0003577	21/22			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-12]
OMIM:176450	Currarino syndrome		HP:0009793	OMIM:176450	TAS					P	HPO:skoehler[2009-02-17]
OMIM:176450	Currarino syndrome		HP:0000006	PMID:9843207	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-12]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000286	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000684	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000365	PMID:22464252	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000486	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0001530	OMIM:101800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0004322	PMID:21651393;PMID:22464252;PMID:22464250	PCS		9/10		HP:0012825	P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000122	PMID:21651393	PCS		1/3			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0010049	PMID:22464250	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0008450	PMID:21651393	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0011342	PMID:22464252	PCS		2/2			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000635	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000316	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000238	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0001847	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0001169	OMIM:101800	TAS					P	HPO:probinson[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0001249	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000995	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0003165	PMID:21651393;PMID:22464250	PCS		8/8			P	HPO:probinson[2020-12-14];HPO:skoehler[2012-10-09];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0011800	PMID:22464252	PCS		2/2			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0004490	OMIM:101800	TAS					P	HPO:probinson[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0003083	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0033579	PMID:21651393	PCS		2/2			P	HPO:probinson[2021-02-13]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0002905	PMID:21651393	PCS		3/3			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000327	PMID:21651393	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000689	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000648	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0005616	PMID:21651393	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000006	PMID:21651393	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000248	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000463	OMIM:101800	TAS					P	HPO:probinson[2012-05-01]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0001156	PMID:21651393;PMID:22464250	PCS		8/8		HP:0012828;HP:0012828	P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0010743	PMID:22464250	IEA		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000858	OMIM:101800	TAS					P	HPO:probinson[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0010230	PMID:22464250	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0008873	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0008479	OMIM:101800	IEA					P	HPO:skoehler[2012-10-09]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0003528	PMID:21651393	PCS		2/2			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000455	OMIM:101800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000851	PMID:22464252	PCS	HP:0003577	1/2			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000135	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0009803	PMID:22464250	PCS		5/5			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0002650	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0004279	PMID:22464252	PCS		2/2			P	HPO:probinson[2012-07-29];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0005280	OMIM:101800;PMID:22464250	PCS		12/15			P	HPO:probinson[2012-05-01];HPO:probinson[2020-12-14];HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0010655	PMID:21651393	PCS		3/3			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0001518	PMID:21651393	PCS	HP:0003577	1/3			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000668	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0002925	PMID:21651393;PMID:22464250	PCS		6/8			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0001511	PMID:22464250	PCS	HP:0011461	1/5			P	HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0003416	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000028	PMID:21651393;PMID:22464252	PCS		3/4	MALE	HP:0012833	P	HPO:probinson[2020-12-14];HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0000303	PMID:22464250	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-14]
OMIM:101800	Acrodysostosis 1, with or without hormone resistance		HP:0005756	OMIM:101800	IEA					P	HPO:iea[2009-02-17]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0025352	PMID:32197074	PCS					I	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0002067	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0000750	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0000012	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0031936	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0001260	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0001252	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0000739	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0003593	PMID:32197074	PCS		1/1			C	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0002061	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0007018	PMID:32197074	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:618878	Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome		HP:0000006	PMID:32197074	PCS					I	HPO:probinson[2022-09-04]
OMIM:617593	Spermatogenic failure 20		HP:0032560	PMID:28552195	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-08]
OMIM:617593	Spermatogenic failure 20		HP:0003251	PMID:28552195	PCS		1/1			P	HPO:probinson[2022-09-08]
OMIM:617593	Spermatogenic failure 20		HP:0011462	PMID:28552195	PCS		1/1			C	HPO:probinson[2022-09-08]
OMIM:617593	Spermatogenic failure 20		HP:0000007	PMID:28552195	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-08]
OMIM:617593	Spermatogenic failure 20		HP:0032558	PMID:28552195	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-08]
OMIM:617593	Spermatogenic failure 20		HP:0032559	PMID:28552195	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-08]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0011968	PMID:11489939	PCS	HP:0003623	1/1			P	HPO:probinson[2022-09-02]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0000825	PMID:11489939;PMID:14693719	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0002173	PMID:11489939	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0002173	PMID:14693719	PCS		1/2			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0001252	PMID:14693719	PCS		1/2			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0000007	PMID:11489939	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0001249	OMIM:609975	IEA					P	HPO:iea[2009-02-17]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0001325	OMIM:609975	IEA					P	HPO:iea[2009-02-17]
OMIM:609975	Hyperinsulinemic hypoglycemia, familial, 4		HP:0003623	PMID:11489939;PMID:14693719	PCS		3/3			C	HPO:probinson[2022-09-02]
OMIM:620459	Birt-Hogg-Dube syndrome 2		HP:0001012	PMID:36440963	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620459	Birt-Hogg-Dube syndrome 2		HP:0030436	PMID:36440963	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620459	Birt-Hogg-Dube syndrome 2		HP:0011462	PMID:36440963	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620459	Birt-Hogg-Dube syndrome 2		HP:0006770	PMID:36440963	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620459	Birt-Hogg-Dube syndrome 2		HP:0032225	PMID:36440963	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620459	Birt-Hogg-Dube syndrome 2		HP:0032445	PMID:36440963	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620459	Birt-Hogg-Dube syndrome 2		HP:0000006	PMID:36440963	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:172150	6-@phosphogluconolactonase deficiency		HP:0001878	OMIM:172150	IEA					P	HPO:iea[2009-02-17]
OMIM:172150	6-@phosphogluconolactonase deficiency		HP:0000006	OMIM:172150	IEA					I	HPO:iea[2009-02-17]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002421	PMID:22492562	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001396	OMIM:614924	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0006989	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002067	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002188	PMID:22492562	PCS		7/8			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001332	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001250	PMID:22492562	PCS		6/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001252	PMID:22492562	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001274	PMID:22492562	PCS		3/11			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002240	OMIM:614924	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0003593	PMID:22492562	PCS		1/1			C	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0031964	PMID:22492562	PCS		1/1			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001508	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0006254	PMID:22492562	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001403	OMIM:614924	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0003128	PMID:22492562	PCS		1/1			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0008936	PMID:22492562	PCS		5/12			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0000175	OMIM:614924	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0031956	PMID:22492562	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001344	PMID:22492562	PCS		7/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0003200	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002376	PMID:22492562	PCS		10/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002079	PMID:22492562	PCS		6/11			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0003487	PMID:22492562	PCS		4/12			P	HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0011924	PMID:22492562	PCS		1/1			P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0011968	PMID:22492562	PCS		3/12			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002352	PMID:22492562	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001263	PMID:22492562	PCS		10/11			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0002151	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001285	PMID:22492562	PCS		9/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0011923	PMID:22492562	PCS		1/1			P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0000508	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0000602	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0000007	PMID:22492562	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0008347	PMID:22492562	PCS		1/1			P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0001319	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614924	Combined oxidative phosphorylation deficiency 12		HP:0000505	OMIM:614924	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613093	Cone dystrophy 4		HP:0000639	PMID:19615668	PCS		7/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0030465	PMID:19615668	PCS		5/6			P	HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0011463	PMID:19615668	PCS		7/7			C	HPO:probinson[2023-01-15];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0000613	PMID:19615668	PCS		5/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0000007	PMID:19615668	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0007663	PMID:19615668	PCS		7/7			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0007641	PMID:19615668	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0000505	PMID:19615668	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0000548	PMID:19615668	PCS					P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-15]
OMIM:613093	Cone dystrophy 4		HP:0030825	PMID:19615668	PCS		5/7			P	HPO:probinson[2023-01-15]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0000252	PMID:19409520	PCS	HP:0003577	1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0004313	PMID:19409520	PCS		0/1			P	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21];HPO:probinson[2024-03-14]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0000540	PMID:19409520	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0004322	PMID:19409520	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0000320	PMID:19409520	IEA	HP:0003577	1/1			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0001251	PMID:19409520	PCS		1/1		HP:0012825	P	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0000007	PMID:19409520	PCS					I	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0001257	PMID:19409520	PCS	HP:0003577	1/1		HP:0012825	P	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0001510	PMID:19409520	PCS		1/1			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0001249	PMID:19409520	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21]
OMIM:613078	Nijmegen breakage syndrome-like disorder		HP:0010997	PMID:19409520	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2020-07-21]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002783	PMID:29729943	PCS		48/131			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002582	PMID:29729943	PCS		8/133			P	HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0001890	PMID:25329329	PCS		4/14			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002240	PMID:29729943	PCS		17/130			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0032216	PMID:25213377	IEA					P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0012393	PMID:25213377	PCS		2/6			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0003829	PMID:29729943	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0100806	PMID:29729943	PCS		10/128			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0001888	PMID:25329329;PMID:25213377	PCS		18/19			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002716	PMID:29729943	PCS		43/130			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0001744	PMID:25329329	PCS		6/12			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0003765	PMID:25329329	PCS		3/14			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0001369	PMID:25329329	PCS		2/14			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0004315	PMID:29729943	PCS		42/116			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002014	PMID:29729943	PCS		51/133			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002850	PMID:29729943	PCS		30/118			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0004313	PMID:29729943	PCS		65/120			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0100280	PMID:29729943	PCS		7/132			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002110	PMID:29729943	PCS		20/124			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0000964	PMID:25213377	PCS		1/6			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002788	PMID:29729943	PCS		41/132			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0001973	PMID:25329329	PCS		5/14			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0000006	PMID:25329329	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002720	PMID:29729943	PCS		53/119			P	HPO:probinson[2020-04-24]
OMIM:616100	Autoimmune lymphoproliferative syndrome, type V		HP:0002721	PMID:25329329	PCS					P	HPO:probinson[2020-04-24]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001276	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0003676	OMIM:610217	IEA					C	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002067	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001310	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001332	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001250	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001272	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002066	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002185	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002180	OMIM:610217	TAS					P	HPO:skoehler[2015-01-21]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002080	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0000639	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0011463	OMIM:610217	TAS					C	HPO:skoehler[2015-12-30]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0000712	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0000736	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0000752	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001268	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001884	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002015	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002059	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0000750	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0003487	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0011968	OMIM:610217	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001260	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002075	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0002072	OMIM:610217	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0100710	OMIM:610217	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0100315	OMIM:610217	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0007772	OMIM:610217	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0000007	OMIM:610217	IEA					I	HPO:skoehler[2010-06-19]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0000648	OMIM:610217	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610217	Neurodegeneration with brain iron accumulation 2B		HP:0001257	OMIM:610217	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300581	FG syndrome 5		HP:0000286	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0000582	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0000343	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0000486	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0000243	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0000463	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0001252	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0003196	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0005280	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0040082	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0011330	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0012450	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0001417	PMID:16283679	PCS					I	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0000047	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0000699	PMID:16283679	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:300581	FG syndrome 5		HP:0003623	PMID:16283679	PCS		1/1			C	HPO:probinson[2023-07-07]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0003577	PMID:10234505;PMID:10383750;PMID:10730767	PCS		13/13			C	HPO:probinson[2021-12-18];HPO:probinson[2022-05-16];HPO:probinson[2021-12-18];HPO:probinson[2022-03-01]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0034067	PMID:10383750;PMID:10730767	PCS		2/2			P	HPO:probinson[2022-02-03];HPO:probinson[2022-05-16];HPO:probinson[2022-03-01]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0008066	PMID:10234505;PMID:8757772;PMID:10383750;PMID:10730767	PCS		14/14			P	HPO:probinson[2021-12-18];HPO:probinson[2022-05-16];HPO:probinson[2021-12-18];HPO:probinson[2022-03-01]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0000972	PMID:10234505	PCS					P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0007446	PMID:10383750	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0033802	PMID:10234505	PCS					P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0200097	PMID:10234505;PMID:8757772;PMID:10383750;PMID:10730767	PCS		14/14			P	HPO:probinson[2021-12-18];HPO:probinson[2022-05-16];HPO:probinson[2021-12-18];HPO:probinson[2022-03-01]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0000006	PMID:1372711	PCS					I	HPO:probinson[2021-12-18]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0034193	PMID:10730767	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:619555	Epidermolysis bullosa simplex 2A, generalized severe		HP:0003623	PMID:8757772	PCS		1/1			C	HPO:probinson[2021-12-18]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0000110	PMID:26235987	PCS		1/12			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0003621	PMID:26235987	PCS		5/12			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0003596	PMID:26235987	PCS		2/12			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0000089	PMID:26235987	PCS		1/12			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0030157	PMID:26235987	PCS		3/12			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0000083	PMID:26235987	PCS		2/12			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0000072	PMID:26235987	PCS		1/12			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0000074	PMID:26235987	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0011463	PMID:26235987	PCS		1/12			C	HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0011462	PMID:26235987	PCS		1/12			C	HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0004719	PMID:26235987	PCS		1/12			P	HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0011461	PMID:26235987	PCS		3/12			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0008676	PMID:26235987	PCS		1/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0003418	PMID:26235987	PCS		1/12			P	HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0000006	PMID:26235987	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:143400	Congenital anomalies of kidney and urinary tract 2		HP:0000126	PMID:26235987	PCS	HP:0011461	2/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0003477	PMID:19805727	PCS		5/9			P	HPO:probinson[2012-04-28]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0002169	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0003676	OMIM:270700	IEA					C	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0003693	OMIM:270700	PCS					P	HPO:probinson[2012-04-06]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000020	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0002064	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0001251	OMIM:270700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0002061	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000639	PMID:19805727	PCS		4/10			P	HPO:probinson[2012-04-28]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0010550	OMIM:270700	PCS					P	HPO:probinson[2012-04-28]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0007340	OMIM:270700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0002839	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000712	OMIM:270700	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0007663	OMIM:270700	TAS					P	HPO:skoehler[2015-07-26]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0001249	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0001347	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000012	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0001761	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0003487	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0002079	OMIM:270700	PCS					P	HPO:probinson[2012-04-06]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0001260	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000709	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0002607	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000608	OMIM:270700	PCS					P	HPO:probinson[2012-04-06]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0001317	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000007	OMIM:270700	IEA					I	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000546	PMID:19805727	PCS		3/7			P	HPO:probinson[2012-04-28]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0000505	OMIM:270700	IEA					P	HPO:iea[2009-02-17]
OMIM:270700	Spastic paraplegia 15, autosomal recessive		HP:0001258	OMIM:270700	PCS					P	HPO:probinson[2012-04-06]
OMIM:614065	Myopathy, distal, 4		HP:0001430	OMIM:614065	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614065	Myopathy, distal, 4		HP:0003202	OMIM:614065	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-29]
OMIM:614065	Myopathy, distal, 4		HP:0001265	OMIM:614065	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614065	Myopathy, distal, 4		HP:0003198	PMID:21620354	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-29]
OMIM:614065	Myopathy, distal, 4		HP:0008180	PMID:21620354	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-29]
OMIM:614065	Myopathy, distal, 4		HP:0011462	PMID:21620354	PCS					C	HPO:probinson[2022-09-29]
OMIM:614065	Myopathy, distal, 4		HP:0001638	OMIM:614065	TAS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-29];HPO:probinson[2022-09-29]
OMIM:614065	Myopathy, distal, 4		HP:0001324	OMIM:614065	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614065	Myopathy, distal, 4		HP:0007149	OMIM:614065	TAS					P	HPO:skoehler[2012-11-19]
OMIM:614065	Myopathy, distal, 4		HP:0003701	OMIM:614065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614065	Myopathy, distal, 4		HP:0003427	PMID:21620354	PCS					P	HPO:probinson[2022-09-29];HPO:probinson[2022-09-29]
OMIM:614065	Myopathy, distal, 4		HP:0000006	PMID:21620354	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614065	Myopathy, distal, 4		HP:0003677	OMIM:614065	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614065	Myopathy, distal, 4		HP:0008944	OMIM:614065	TAS					P	HPO:skoehler[2012-11-18]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002069	PMID:25361775	PCS		2/2			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0000365	PMID:25361775	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001332	PMID:25787132	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002120	PMID:25787132	PCS		1/1			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001272	PMID:25787132	PCS		1/1			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0006829	OMIM:616672	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001252	PMID:25787132	PCS		1/1			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002283	PMID:25361775	PCS		1/2			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0003593	PMID:25787132	PCS		1/1			C	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0010841	OMIM:616672	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0033725	PMID:25787132	PCS		1/1			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001508	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001987	PMID:25361775	PCS		2/2			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001268	PMID:25361775	PCS		2/2			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002179	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0000252	OMIM:616672	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0003621	PMID:25361775	PCS		2/2			C	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002059	OMIM:616672	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002133	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002079	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001321	OMIM:616672	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0011968	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0011924	PMID:25787132	PCS		1/1			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002151	PMID:25361775	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001263	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002273	PMID:25361775	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0005484	OMIM:616672	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001284	OMIM:616672	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0002072	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0011923	PMID:25787132	PCS		1/1			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0000007	PMID:25361775	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0000505	PMID:25361775	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0200134	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0008347	PMID:25787132	PCS		1/1			P	HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001414	PMID:25787132	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23]
OMIM:616672	Combined oxidative phosphorylation deficiency 27		HP:0001336	PMID:25787132;PMID:25361775	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-23];HPO:probinson[2022-05-23]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0004467	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000384	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0004322	PMID:33276377	PCS		3/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000122	PMID:33276377	PCS		1/9			P	HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0003298	PMID:33276377	PCS		1/6			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0002162	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000957	PMID:33276377	PCS		1/9			P	HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000998	PMID:33276377	PCS		1/9			P	HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000337	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000912	PMID:33276377	PCS		4/9			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000278	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0002575	PMID:33276377	PCS		6/12			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000176	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000252	PMID:33276377	PCS		1/9			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000453	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0002032	PMID:33276377	PCS		6/12			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0001263	PMID:33276377	PCS		3/9			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0011623	PMID:33276377	PCS		2/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0002949	PMID:33276377	PCS		2/6			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000767	PMID:33276377	PCS		1/7			P	HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0003316	PMID:33276377	PCS		3/6			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0001357	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0007018	PMID:33276377	PCS		2/9			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000465	PMID:33276377	PCS		1/11		HP:0012825	P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000006	PMID:33276377	PCS					I	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0002247	PMID:33276377	PCS		2/12			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000369	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000445	PMID:33276377	PCS		1/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:619227	Vertebral, cardiac, tracheoesophageal, renal, and limb defects		HP:0000104	PMID:33276377	IEA		2/9			P	HPO:probinson[2021-05-27]
OMIM:274200	Thumb, distal hyperextensibility of		HP:0005722	OMIM:274200	IEA					P	HPO:iea[2009-02-17]
OMIM:274200	Thumb, distal hyperextensibility of		HP:0000007	OMIM:274200	IEA					I	HPO:iea[2009-02-17]
OMIM:600776	Fryns microphthalmia syndrome		HP:0100336	OMIM:600776	TAS					P	HPO:probinson[2024-03-08]
OMIM:600776	Fryns microphthalmia syndrome		HP:0100337	OMIM:600776	TAS					P	HPO:probinson[2024-03-08]
OMIM:600776	Fryns microphthalmia syndrome		HP:0000528	OMIM:600776	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600776	Fryns microphthalmia syndrome		HP:0045005	OMIM:600776	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600776	Fryns microphthalmia syndrome		HP:0000007	OMIM:600776	IEA					I	HPO:iea[2009-02-17]
OMIM:600776	Fryns microphthalmia syndrome		HP:0000568	OMIM:600776	IEA					P	HPO:skoehler[2015-01-21]
OMIM:600776	Fryns microphthalmia syndrome		HP:0031909	OMIM:600776	TAS					P	HPO:probinson[2024-03-08]
OMIM:600776	Fryns microphthalmia syndrome		HP:0000400	OMIM:600776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600776	Fryns microphthalmia syndrome		HP:0002006	OMIM:600776	IEA					P	HPO:skoehler[2010-06-20]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001792	PMID:20080219	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0010804	OMIM:239300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000582	PMID:20080219	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000365	OMIM:239300	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001795	OMIM:239300	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0002120	OMIM:239300	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001250	PMID:20080219	PCS		3/5			P	HPO:iea[2009-02-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0003155	PMID:20080219	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001252	PMID:20080219	PCS	HP:0003593	5/5			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0003196	OMIM:239300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001290	OMIM:239300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0012448	PMID:17351347	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001090	PMID:20080219	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0012210	OMIM:239300	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0009882	PMID:20080219	PCS		7/7			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000316	PMID:20080219	PCS		6/7			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000238	PMID:20080219	PCS		1/3			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001627	OMIM:239300	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000637	PMID:20080219	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000219	PMID:20080219	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0002714	PMID:20080219	PCS		6/7			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000455	PMID:20080219	PCS		6/7			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0002019	PMID:20080219	PCS		2/5			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001249	PMID:20080219	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000358	PMID:20080219	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001545	PMID:20080219	PCS		2/5			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0002553	OMIM:239300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000175	PMID:20080219	TAS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-07-03]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0002034	PMID:20080219	TAS		4/7			P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001344	PMID:20080219	TAS		6/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2019-07-03]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000750	OMIM:239300	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000431	PMID:20080219	PCS		6/7			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0011968	OMIM:239300	TAS		HP:0040283			P	HPO:nvasilevsky[2019-03-29];HPO:nvasilevsky[2019-03-29];HPO:probinson[2019-07-03]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001263	PMID:20080219	TAS		7/7			P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0002251	PMID:20080219	PCS		1/7			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000272	OMIM:239300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0011800	OMIM:239300	TAS					P	HPO:skoehler[2013-11-28]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001182	OMIM:239300	TAS					P	HPO:skoehler[2013-05-31]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000407	PMID:20080219	PCS		2/3			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000007	PMID:20080219	PCS					I	HPO:iea[2009-02-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001357	OMIM:239300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0002305	OMIM:239300	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000322	OMIM:239300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000204	PMID:20080219	PCS		1/7			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001216	PMID:20080219	PCS		2/3			P	HPO:iea[2010-02-15]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0000303	OMIM:239300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239300	Hyperphosphatasia with impaired intellectual development syndrome 1		HP:0001831	OMIM:239300	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:617222	Sudden cardiac failure, infantile		HP:0012819	PMID:27523598	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001685	PMID:27523598	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001662	PMID:27523598	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001250	OMIM:617222	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001639	PMID:27523598	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0011463	PMID:27523598	PCS		5/7			C	HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001252	PMID:27523598	PCS		1/7			P	HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0003593	PMID:27523598	PCS		2/7			C	HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0000007	PMID:27523598	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001635	OMIM:617222	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001942	OMIM:617222	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617222	Sudden cardiac failure, infantile		HP:0001645	PMID:27523598	PCS		7/7			P	HPO:probinson[2022-09-24]
OMIM:223370	Dubowitz syndrome		HP:0000286	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000486	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000684	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0004322	PMID:18990984	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0000485	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0001252	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0003593	PMID:18990984	PCS		1/1			C	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0002020	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0012745	OMIM:223370	TAS					P	HPO:skoehler[2014-03-24]
OMIM:223370	Dubowitz syndrome		HP:0001290	OMIM:223370	TAS					P	HPO:skoehler[2017-07-13]
OMIM:223370	Dubowitz syndrome		HP:0012471	PMID:18990984	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0000954	PMID:18990984	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0008897	OMIM:223370	PCS					P	HPO:probinson[2012-03-16]
OMIM:223370	Dubowitz syndrome		HP:0000510	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000752	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0001763	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0001249	OMIM:223370	PCS					P	HPO:probinson[2012-03-16];HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0004315	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000176	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000252	PMID:18990984	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0002750	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0001263	PMID:18990984	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0009891	OMIM:223370	TAS					P	HPO:probinson[2012-03-16]
OMIM:223370	Dubowitz syndrome		HP:0000568	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000964	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000007	OMIM:223370	IEA					I	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0007676	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0004209	PMID:18990984	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0000960	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000047	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000325	PMID:18990984	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0002665	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000369	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0005338	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000324	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0002028	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0006349	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000220	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000340	OMIM:223370	TAS					P	HPO:probinson[2012-05-01]
OMIM:223370	Dubowitz syndrome		HP:0000023	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000540	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000581	OMIM:223370	PCS		20/20			P	HPO:probinson[2012-03-16];HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0002719	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000612	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0008872	PMID:18990984	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0000736	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000218	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000411	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000455	PMID:18990984	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0001620	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0003006	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000274	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000670	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000431	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000750	OMIM:223370	TAS					P	HPO:probinson[2012-03-16]
OMIM:223370	Dubowitz syndrome		HP:0003146	PMID:18990984	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0002572	OMIM:223370	TAS					P	HPO:skoehler[2013-05-29]
OMIM:223370	Dubowitz syndrome		HP:0001915	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000506	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000508	PMID:18990984	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0002209	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000426	PMID:18990984	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:223370	Dubowitz syndrome		HP:0000348	OMIM:223370	TAS					P	HPO:probinson[2012-05-01]
OMIM:223370	Dubowitz syndrome		HP:0001159	OMIM:223370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:223370	Dubowitz syndrome		HP:0001511	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000388	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0006721	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000347	OMIM:223370	PCS					P	HPO:probinson[2012-03-16]
OMIM:223370	Dubowitz syndrome		HP:0002720	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:223370	Dubowitz syndrome		HP:0000028	OMIM:223370	IEA					P	HPO:iea[2009-02-17]
OMIM:138930	Grant syndrome		HP:0002982	OMIM:138930	IEA					P	HPO:skoehler[2010-06-20]
OMIM:138930	Grant syndrome		HP:0000592	OMIM:138930	IEA					P	HPO:iea[2009-02-17]
OMIM:138930	Grant syndrome		HP:0002645	OMIM:138930	IEA					P	HPO:skoehler[2010-06-20]
OMIM:138930	Grant syndrome		HP:0200021	OMIM:138930	IEA					P	HPO:iea[2009-02-17]
OMIM:138930	Grant syndrome		HP:0000006	OMIM:138930	IEA					I	HPO:iea[2009-02-17]
OMIM:138930	Grant syndrome		HP:0000347	OMIM:138930	IEA					P	HPO:iea[2009-02-17]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0008936	PMID:20833646	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0011097	PMID:20833646	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0002069	PMID:20833646	PCS	HP:0011463	1/1			P	HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0002521	PMID:20833646	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0002376	PMID:20833646	PCS	HP:0011463	1/1			P	HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0032792	PMID:20833646	PCS	HP:0011463	1/1			P	HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0003593	PMID:20833646	PCS		1/1			C	HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0000007	PMID:20833646	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0200134	PMID:20833646	PCS		1/1			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0007359	PMID:20833646	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0001257	PMID:20833646	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-25]
OMIM:613722	Developmental and epileptic encephalopathy 12		HP:0001347	OMIM:613722	TAS					P	HPO:skoehler[2012-10-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0001254	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0002024	OMIM:238750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0003168	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0003297	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0001987	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0002161	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0000007	OMIM:238750	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0001510	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0001249	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:238750	Hyperlysinuria with hyperammonemia		HP:0001259	OMIM:238750	IEA					P	HPO:iea[2009-02-17]
OMIM:616882	Advanced sleep phase syndrome, familial, 3		HP:0000716	PMID:26903630	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-21]
OMIM:616882	Advanced sleep phase syndrome, familial, 3		HP:0031873	PMID:26903630	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:616882	Advanced sleep phase syndrome, familial, 3		HP:0000006	PMID:26903630	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-21]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0001276	PMID:31585108	PCS		4/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0002521	PMID:31585108	PCS		1/9			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0002510	PMID:31585108	PCS		3/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0000750	PMID:31585108	PCS		11/11			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0002079	PMID:31585108	PCS		11/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0001321	PMID:31585108	PCS		2/12		HP:0012825	P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0002365	PMID:31585108	PCS		2/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0002197	PMID:31585108	PCS		7/8			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0001263	PMID:31585108	PCS					P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0001252	PMID:31585108	PCS		10/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0003593	PMID:31585108	PCS					C	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0032794	PMID:31585108	PCS		7/8			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0002194	PMID:31585108	PCS		12/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0010862	PMID:31585108	PCS		12/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0012434	PMID:31585108	PCS		12/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0012469	PMID:31585108	PCS		1/8			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0032390	PMID:31585108	PCS		5/9			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0012110	PMID:31585108	PCS		2/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0006891	PMID:31585108	PCS					P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0001339	PMID:31585108	PCS		12/12			P	HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0000007	PMID:31585108	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618677	Cortical dysplasia, complex, with other brain malformations 10		HP:0002119	PMID:31585108	PCS		12/12			P	HPO:probinson[2020-07-23]
OMIM:182260	Slipped femoral capital epiphyses		HP:0006461	OMIM:182260	TAS					P	HPO:skoehler[2009-02-17]
OMIM:182260	Slipped femoral capital epiphyses		HP:0008843	OMIM:182260	TAS					P	HPO:skoehler[2009-02-17]
OMIM:182260	Slipped femoral capital epiphyses		HP:0000006	OMIM:182260	TAS					I	HPO:skoehler[2012-07-28]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0003202	PMID:26561570	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0002179	PMID:26561570	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0001276	PMID:26561570	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0008936	PMID:26561570	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0003577	PMID:26561570	PCS		2/2			C	HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0002151	PMID:26561570	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0002490	PMID:26561570	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0012736	PMID:26561570	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0011410	PMID:26561570	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0011923	PMID:26561570	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0009141	PMID:26561570	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0000407	PMID:26561570	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0001639	PMID:26561570	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0000546	PMID:26561570	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0008872	PMID:26561570	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0000007	PMID:26561570	PCS					I	HPO:probinson[2017-06-23]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0008347	PMID:26561570	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0000648	PMID:26561570	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0001612	PMID:26561570	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0001623	PMID:26561570	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0002104	PMID:26561570	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2024-03-15]
OMIM:616896	Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)		HP:0003348	PMID:26561570	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0007759	PMID:16606891	PCS		2/2			P	HPO:probinson[2013-02-22];HPO:probinson[2021-10-24]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0007957	PMID:9727509	PCS		7/7			P	HP:probinson[2021-10-24]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0000486	OMIM:608470	TAS					P	HPO:probinson[2013-02-22]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0001131	PMID:9727509;PMID:16606891	PCS		9/9			P	HP:probinson[2021-10-24];HPO:probinson[2013-01-09];HPO:probinson[2021-10-24]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0003593	PMID:16606891	PCS		2/2			C	HPO:probinson[2021-10-24]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0000613	PMID:16606891	PCS		1/2			P	HPO:probinson[2013-02-22];HPO:probinson[2021-10-24]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0007663	PMID:9727509	PCS		3/7			P	HP:probinson[2021-10-24]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0200020	PMID:16606891	PCS		2/2			P	HPO:probinson[2013-02-22];HPO:probinson[2021-10-24]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0000006	PMID:9054935	PCS					I	HPO:probinson[2013-02-22]
OMIM:608470	Corneal dystrophy, Reis-Bucklers type		HP:0100540	PMID:16606891	PCS		1/2			P	HPO:probinson[2021-10-24]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0002058	PMID:31688942	PCS		4/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0000286	PMID:31688942	PCS		6/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0003577	PMID:31688942	PCS					C	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0000494	PMID:31688942	PCS		6/6		HP:0012825	P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0002266	PMID:31688942	PCS		2/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0000350	PMID:31688942	PCS		4/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0006829	PMID:31688942	PCS		6/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0001263	PMID:31688942	PCS		6/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0032794	PMID:31688942	PCS		3/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0010851	PMID:31688942	PCS		6/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0012469	PMID:31688942	PCS		5/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0000407	PMID:31688942	PCS		5/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0032792	PMID:31688942	PCS		3/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0011120	PMID:31688942	PCS		4/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0009830	PMID:31688942	PCS		5/5			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0000007	PMID:31688942	PCS					I	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0000218	PMID:31688942	PCS		4/6			P	HPO:probinson[2020-07-20]
OMIM:618663	Epileptic encephalopathy, early infantile, 81		HP:0000268	PMID:31688942	PCS		2/6			P	HPO:probinson[2020-07-20]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0001056	PMID:11710919	PCS		0/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-16]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0034194	PMID:11710919	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0008066	PMID:11710919	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-16]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0003593	PMID:11710919	PCS					C	HPO:probinson[2022-03-16]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0000972	PMID:11710919	PCS		2/5			P	HPO:skoehler[2010-06-18];HP:probinson[2019-03-03];HPO:probinson[2022-03-16]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0008404	PMID:11710919	PCS		0/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-03-16]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0000006	PMID:7682883	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-03]
OMIM:131900	Epidermolysis bullosa simplex 1B, generalized intermediate		HP:0200097	PMID:11710919	PCS		0/5			P	HP:probinson[2019-03-03];HPO:probinson[2022-03-16]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0003577	PMID:20814945	PCS		4/4			C	HPO:probinson[2022-05-08]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0001596	PMID:20814945	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0002231	PMID:20814945	PCS		3/4			P	HPO:iea[2012-03-01];HPO:probinson[2022-05-08]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0030056	PMID:20814945	PCS		1/1			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0002209	PMID:20814945	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0000653	PMID:20814945	PCS					P	HPO:iea[2012-03-01];HPO:probinson[2022-05-08]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0045075	PMID:20814945	PCS	HP:0003577	4/4			P	HPO:probinson[2022-05-08]
OMIM:146550	Marie unna hereditary hypotrichosis 1		HP:0000006	PMID:19122663	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0003621	PMID:21412258	PCS		3/3			C	HPO:probinson[2023-04-19]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0012322	OMIM:613736	IEA					P	HPO:probinson[2013-01-09]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0002860	OMIM:613736	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0040154	PMID:21412258	PCS		3/3			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-04-19]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0011132	PMID:21412258	PCS		3/3			P	HPO:probinson[2013-08-11];HPO:probinson[2023-04-19]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0100838	PMID:21412258	PCS		3/3			P	HPO:probinson[2013-08-11];HPO:probinson[2023-04-19]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0007502	OMIM:613736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613736	Acne inversa, familial, 2, with or without dowling-degos disease		HP:0000006	PMID:20929727	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-19]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001166	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0002058	OMIM:609008	TAS					P	HPO:probinson[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001132	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001187	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001696	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0002650	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0002870	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0000276	OMIM:609008	TAS					P	HPO:probinson[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0005301	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001519	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0002808	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0002816	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0002616	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0000768	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001659	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0003745	OMIM:609008	IEA					I	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001642	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0000303	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0000545	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:609008	Marfanoid habitus with situs inversus		HP:0001634	OMIM:609008	IEA					P	HPO:iea[2009-02-17]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0012047	PMID:27588451	PCS	HP:0011462	1/3			P	HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0000639	PMID:27588451	PCS	HP:0003581	1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0000407	PMID:27588451	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0011463	PMID:27588451	PCS		2/3			C	HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0000608	PMID:27588451	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0011462	PMID:27588451	PCS		1/3			C	HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0000613	PMID:27588451	PCS	HP:0003581	1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0000007	PMID:27588451	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0007641	PMID:27588451	PCS		1/3			P	HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0000505	PMID:27588451	PCS		3/3			P	HPO:probinson[2020-12-02]
OMIM:617236	Cone-rod dystrophy and hearing loss		HP:0001105	PMID:27588451	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-02]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0000175	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0001795	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0000162	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0009882	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0000348	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0001182	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0001417	OMIM:311895	IEA					I	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0004209	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0002007	OMIM:311895	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0000201	OMIM:311895	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0005747	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:311895	Pierre Robin sequence with facial and digital anomalies		HP:0000347	OMIM:311895	IEA					P	HPO:iea[2009-02-17]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0002384	PMID:34185323	PCS		5/11			P	HPO:probinson[2023-02-06];HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0010819	PMID:34185323	PCS		5/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0002121	PMID:34185323	PCS		7/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0003593	PMID:34185323	PCS		7/11			C	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0032794	PMID:34185323	PCS		5/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0025190	PMID:34185323	PCS		6/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0032663	PMID:34185323	PCS		1/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0012506	PMID:34185323	PCS		4/5			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0033725	PMID:34185323	PCS		3/5			P	HPO:probinson[2023-02-06];HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0011463	PMID:34185323	PCS		4/11			C	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0032792	PMID:34185323	PCS		6/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0032660	PMID:34185323	PCS		2/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0007334	PMID:34185323	PCS		1/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0200134	PMID:34185323	PCS		11/11			P	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0000006	PMID:34185323	PCS					I	HPO:probinson[2023-02-06]
OMIM:620115	Developmental and epileptic encephalopathy 108		HP:0001249	PMID:34185323	PCS		11/11			P	HPO:probinson[2023-02-06]
OMIM:617961	Spermatogenic failure 26		HP:0003251	PMID:28905369	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:617961	Spermatogenic failure 26		HP:0011462	PMID:28905369	PCS		1/1			C	HPO:probinson[2023-02-07]
OMIM:617961	Spermatogenic failure 26		HP:0000007	PMID:28905369	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:617961	Spermatogenic failure 26		HP:0012869	PMID:28905369	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000286	PMID:25846674	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000365	PMID:25316788	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0004322	PMID:25846674	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001250	PMID:26290468;PMID:25316788	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0002066	PMID:26290468	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000160	PMID:25846674	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001252	PMID:25316788	PCS		3/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001251	PMID:25846674	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0002020	PMID:25316788;PMID:25846674	PCS		4/7			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02];HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0030891	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001290	PMID:25846674	PCS	HP:0003623	1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0009381	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0009540	PMID:25316788	PCS		1/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000319	PMID:26290468	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0011461	PMID:25846674	PCS		3/4			C	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000954	PMID:25316788;PMID:25846674	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000678	PMID:25316788	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001769	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0008734	PMID:25846674	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000510	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001249	PMID:25846674	PCS		4/4			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001601	PMID:25316788	PCS		1/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0002655	PMID:26290468	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000252	PMID:25316788;PMID:25846674	PCS		5/7			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001263	PMID:25846674	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001182	PMID:25316788	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0011003	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001419	PMID:25316788	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0004209	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0008689	PMID:25846674	PCS		2/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000047	PMID:25316788	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001337	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0003577	PMID:25846674	PCS		1/4			C	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000343	PMID:26290468	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000540	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000023	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0010621	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0011234	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000939	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0034042	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0002719	PMID:25316788	PCS		3/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001629	PMID:25316788	PCS		1/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0005709	PMID:25316788	PCS		2/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0008872	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000219	PMID:25316788	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0002359	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000411	PMID:26290468;PMID:25316788;PMID:25846674	PCS		4/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0004415	PMID:25316788	PCS		1/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001622	PMID:25316788	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001561	PMID:25846674	PCS	HP:0011461	3/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000750	PMID:26290468;PMID:25846674	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0002650	PMID:26290468	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000431	PMID:25846674	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001321	PMID:26290468	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0031936	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0002373	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0011787	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0012520	PMID:25846674	PCS		1/4			P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000308	PMID:26290468	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001319	PMID:26290468	PCS	HP:0003623	1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000268	PMID:26290468	PCS		3/4			P	HPO:probinson[2021-10-02];HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001511	PMID:26290468	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0004626	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001631	PMID:25316788	PCS		1/3			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0001510	PMID:26290468;PMID:25316788	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000028	PMID:25316788	PCS		3/3	MALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000028	PMID:26290468	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:300998	Intellectual developmental disorder, X-linked syndromic 35		HP:0000303	PMID:25316788	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:212350	Sengers syndrome		HP:0008209	PMID:22277967	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0000486	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0001695	PMID:22277967	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0003198	OMIM:212350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212350	Sengers syndrome		HP:0001252	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0003593	PMID:22277967	PCS		1/2			C	HPO:skoehler[2010-06-19]
OMIM:212350	Sengers syndrome		HP:0001290	OMIM:212350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:212350	Sengers syndrome		HP:0001270	PMID:22277967	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0009141	PMID:22277967	PCS		2/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0000518	PMID:22277967	PCS		2/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0000639	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0000938	PMID:22277967	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0000519	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0001324	OMIM:212350	IEA					P	HPO:skoehler[2010-06-18]
OMIM:212350	Sengers syndrome		HP:0001268	PMID:22277967	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0001645	PMID:22277967	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0003546	OMIM:212350	IEA					P	HPO:skoehler[2010-06-18]
OMIM:212350	Sengers syndrome		HP:0003128	PMID:22277967	PCS		2/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0003623	PMID:22277967	PCS		1/2			C	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0003324	PMID:22277967	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0003388	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0011924	PMID:22277967	PCS		2/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0002151	OMIM:212350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212350	Sengers syndrome		HP:0002092	PMID:22277967	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0011923	PMID:22277967	PCS		2/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0002093	PMID:22277967	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0012378	OMIM:212350	TAS					P	HPO:skoehler[2013-10-22]
OMIM:212350	Sengers syndrome		HP:0001639	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0000007	PMID:22277967	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0008347	PMID:22277967	PCS		2/2			P	HPO:probinson[2023-04-04]
OMIM:212350	Sengers syndrome		HP:0003737	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0004901	OMIM:212350	IEA					P	HPO:iea[2009-02-17]
OMIM:212350	Sengers syndrome		HP:0001510	OMIM:212350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212350	Sengers syndrome		HP:0001873	PMID:22277967	PCS		1/2			P	HPO:skoehler[2012-11-18]
OMIM:212350	Sengers syndrome		HP:0000501	PMID:22277967	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:212350	Sengers syndrome		HP:0000545	OMIM:212350	IEA					P	HPO:skoehler[2010-06-18]
OMIM:212350	Sengers syndrome		HP:0003535	OMIM:212350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002751	PMID:20362275	PCS	HP:0011463	19/19			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002751	PMID:22107750	PCS		3/3			P	HPO:probinson[2024-03-14]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000365	PMID:20362275	PCS		0/19			P	HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002650	OMIM:610968	IEA					P	HPO:iea[2009-02-17]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0004586	OMIM:610968	IEA					P	HPO:iea[2009-02-17]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0003179	OMIM:610968	IEA					P	HPO:iea[2009-02-17]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0004322	OMIM:610968	IEA		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0001382	OMIM:610968	IEA		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0003155	PMID:20362275	PCS		2/19			P	HPO:probinson[2012-07-22];HPO:probinson[2024-03-14]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000592	PMID:20362275	PCS		0/19			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000592	PMID:22107750	PCS	HP:0011463	3/3			P	HPO:probinson[2024-03-14]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0003593	PMID:20362275	PCS		19/19			C	HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000938	PMID:20362275	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0008422	PMID:20362275	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000007	PMID:20362275	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002812	PMID:20362275	PCS		3/19			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000703	PMID:22107750;PMID:20362275	PCS		3/22			P	HPO:probinson[2024-03-14];HPO:skoehler[2013-01-22];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002757	PMID:20362275	PCS		19/19			P	HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002659	PMID:22107750	PCS		3/3			P	HPO:probinson[2012-07-22];HPO:probinson[2024-03-14]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002953	OMIM:610968	IEA					P	HPO:iea[2009-02-17]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0002645	PMID:20362275	PCS		3/19			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-06-05]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000248	OMIM:610968	TAS					P	HPO:skoehler[2015-02-22]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000325	OMIM:610968	TAS					P	HPO:skoehler[2015-02-22]
OMIM:610968	Osteogenesis imperfecta, type XI		HP:0000951	PMID:20362275	PCS		0/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001377	PMID:7815423	PCS		94/109			P	HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0100490	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		10/14			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0003273	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:7815423;PMID:30147916;PMID:9714438	PCS		32/121			P	HPO:probinson[2009-02-17];HPO:probinson[2021-05-27];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0008453	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0009465	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0002616	PMID:8900230;PMID:10797416;PMID:9106527;OMIM:121050;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		11/22			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001647	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001643	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001840	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0009901	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:27625873;PMID:9737771;PMID:9199560;PMID:11754102;PMID:7815423;PMID:30147916;PMID:9714438	PCS		90/119			P	HPO:probinson[2010-06-20];HPO:probinson[2021-05-27];HPO:probinson[2021-05-27];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0002751	PMID:7815423	PCS	HP:0003577	48/105			P	HPO:probinson[2012-09-18];HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0003042	PMID:8900230;PMID:10797416;PMID:9106527;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001181	PMID:7815423	PCS		42/90			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0012774	PMID:27625873	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0012385	PMID:27625873;PMID:7815423	PCS		86/110			P	HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0006380	PMID:27625873	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0034671	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		7/14			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000767	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0008962	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000768	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		4/14			P	HPO:iea[2009-02-17];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0002987	PMID:27625873	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001653	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000006	PMID:11754102	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-09-04]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000248	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0034391	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		10/14			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0030799	PMID:7815423	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0003577	PMID:8900230;PMID:9106527;PMID:11754102;PMID:30147916;PMID:9714438	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2022-03-15]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001270	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001629	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000938	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0002999	PMID:11754102	PCS		2/20			P	HPO:iea[2009-02-17];HPO:probinson[2019-09-04]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000218	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:7815423;PMID:30147916;PMID:9714438	PCS		30/102			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-27];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001166	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:27625873;PMID:9737771;PMID:9199560;PMID:11754102;PMID:7815423;PMID:30147916;PMID:9714438	PCS		104/124			P	HPO:iea[2009-02-17];HPO:probinson[2019-09-04];HPO:probinson[2021-05-27];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0002650	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:27625873;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		11/15			P	HPO:probinson[2021-05-27];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001762	PMID:27625873;PMID:7815423	PCS		29/102			P	HPO:probinson[2021-05-27];HPO:probinson[2009-02-17];HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0003066	PMID:7815423	PCS		38/45			P	HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0005684	OMIM:121050	IEA					P	HPO:skoehler[2015-01-21]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000470	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0010499	PMID:8900230;PMID:10797416;PMID:9106527;OMIM:121050;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		12/22			P	HPO:skoehler[2010-06-18];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001083	PMID:16740166	PCS		HP:0040284			P	HPO:iea[2009-02-17];HPO:probinson[2019-09-04]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001519	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001239	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:27625873;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		3/15			P	HPO:probinson[2021-05-27];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0006487	PMID:7815423	PCS		25/79			P	HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001836	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000268	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0002007	PMID:7815423	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001631	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0005879	PMID:27625873	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000347	PMID:8900230;PMID:10797416;PMID:9106527;PMID:7493032;PMID:27625873;PMID:9737771;PMID:9199560;PMID:11754102;PMID:7815423;PMID:30147916;PMID:9714438	PCS		26/94			P	HPO:probinson[2021-05-27];HPO:probinson[2009-02-17];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0001634	PMID:8900230;PMID:10797416;PMID:9106527;OMIM:121050;PMID:9737771;PMID:9199560;PMID:11754102;PMID:30147916;PMID:9714438	PCS		11/22			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:121050	Contractural arachnodactyly, congenital		HP:0000545	OMIM:121050	IEA					P	HPO:iea[2009-02-17]
OMIM:152900	Lymphedema and cerebral arteriovenous anomaly		HP:0100659	OMIM:152900	TAS					P	HPO:probinson[2009-02-17]
OMIM:152900	Lymphedema and cerebral arteriovenous anomaly		HP:0002092	OMIM:152900	TAS					P	HPO:skoehler[2010-06-20]
OMIM:152900	Lymphedema and cerebral arteriovenous anomaly		HP:0001004	OMIM:152900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:152900	Lymphedema and cerebral arteriovenous anomaly		HP:0000006	OMIM:152900	TAS					I	HPO:probinson[2009-02-17]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0000011	PMID:33855352	PCS		4/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0003621	PMID:33855352	PCS		3/7			C	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0002015	PMID:33855352	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0004389	PMID:33855352	PCS		7/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0001310	PMID:33855352	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0001272	PMID:33855352	PCS		4/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0033725	PMID:33855352	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0025708	PMID:33855352	PCS		2/7			C	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0002719	PMID:33855352	PCS		2/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0000518	PMID:33855352	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0011463	PMID:33855352	PCS		2/7			C	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0000608	PMID:33855352	PCS		3/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0000007	PMID:33855352	PCS					I	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0007256	PMID:33855352	PCS		3/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0006994	PMID:33855352	PCS		6/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0002315	PMID:33855352	PCS		5/5			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0001268	PMID:33855352	PCS		2/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0002401	PMID:33855352	PCS		2/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0004305	PMID:33855352	PCS		2/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0001336	PMID:33855352	PCS		2/7			P	HPO:probinson[2022-05-29]
OMIM:619780	Mitochondrial DNA depletion syndrome 20 (MNGIE type)		HP:0003689	PMID:33855352	PCS		3/3			P	HPO:probinson[2022-05-29]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0002069	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0032989	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0002521	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0000750	PMID:33833240	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0031936	PMID:33833240	PCS		2/2			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0002384	PMID:33833240	PCS		2/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0001250	PMID:33833240	PCS		2/2			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0002033	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0001263	PMID:33833240	PCS		2/2			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0003593	PMID:33833240	PCS		2/2			C	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0011097	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0000729	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0032792	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0020221	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0100716	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0000505	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0000713	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0000752	PMID:33833240	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0000006	PMID:33833240	PCS					I	HPO:probinson[2022-08-20]
OMIM:619970	Developmental and epileptic encephalopathy 104		HP:0001249	PMID:33833240	PCS		2/2			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:245552	Lambotte syndrome		HP:0000252	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000486	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000160	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0001629	OMIM:245552	TAS					P	HPO:skoehler[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000506	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000316	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000007	OMIM:245552	IEA					I	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0002507	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000400	OMIM:245552	TAS					P	HPO:skoehler[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0001511	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0001841	OMIM:245552	TAS		20/20			P	HPO:probinson[2013-12-21];HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000444	OMIM:245552	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245552	Lambotte syndrome		HP:0000278	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0007700	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:245552	Lambotte syndrome		HP:0000413	OMIM:245552	IEA					P	HPO:iea[2009-02-17]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0003676	PMID:19646678	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0003577	PMID:19646678	PCS		1/2			C	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0003693	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002120	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001252	PMID:19646678	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001251	PMID:19646678	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002380	PMID:19646678	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001270	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002280	PMID:19646678	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0012110	PMID:19646678	PCS		1/2			P	HPO:probinson[2014-04-22];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0007141	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0011461	PMID:19646678	IEA		1/2			C	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0200147	OMIM:607596	TAS					P	HPO:skoehler[2013-06-13]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0008872	OMIM:607596	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001308	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0006850	OMIM:607596	IEA					P	HPO:iea[2009-02-17]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0007269	OMIM:607596	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001324	OMIM:607596	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0004878	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001249	OMIM:607596	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001348	PMID:19646678	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001347	OMIM:607596	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0007108	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0006999	OMIM:607596	TAS					P	HPO:probinson[2013-12-20]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001760	OMIM:607596	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0000252	PMID:19646678	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002378	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0003445	OMIM:607596	IEA					P	HPO:iea[2009-02-17]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002015	PMID:19646678	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0006956	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001762	PMID:19646678	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002398	OMIM:607596	IEA					P	HPO:iea[2009-02-17]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001321	PMID:19646678	PCS		2/2			P	HPO:probinson[2014-04-22];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002033	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0001263	OMIM:607596;PMID:19646678	PCS		11/12			P	HPO:skoehler[2019-02-22];HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002070	PMID:19646678	PCS		1/2			P	HPO:probinson[2022-05-14]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002093	OMIM:607596	IEA					P	HPO:iea[2009-02-17]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0002803	OMIM:607596	IEA					P	HPO:iea[2009-02-17]
OMIM:607596	Pontocerebellar hypoplasia type 1A		HP:0000007	PMID:19646678	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0001298	PMID:9266722	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0003596	PMID:9266722	PCS		8/9			C	HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0001300	PMID:9266722	PCS		6/9			P	HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0002354	PMID:9266722	PCS		3/9			P	HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0002185	PMID:9266722	PCS		0/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0002171	PMID:9266722	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0000726	PMID:9266722	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0006790	PMID:9266722	PCS		3/3			P	HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0000718	PMID:9266722	PCS		4/9			P	HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0025710	PMID:9266722	PCS		1/9			C	HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0000751	PMID:9266722	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0000006	PMID:9266722	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:606688	Spongiform encephalopathy with neuropsychiatric features		HP:0000710	PMID:9266722	PCS		5/9			P	HPO:probinson[2023-02-21]
OMIM:120400	Coloboma of macula with type B brachydactyly		HP:0005831	OMIM:120400	IEA					P	HPO:iea[2009-02-17]
OMIM:120400	Coloboma of macula with type B brachydactyly		HP:0005807	OMIM:120400	TAS					P	HPO:probinson[2009-02-17]
OMIM:120400	Coloboma of macula with type B brachydactyly		HP:0009642	OMIM:120400	TAS					P	HPO:probinson[2012-06-09]
OMIM:120400	Coloboma of macula with type B brachydactyly		HP:0009611	OMIM:120400	TAS					P	HPO:skoehler[2012-11-16]
OMIM:120400	Coloboma of macula with type B brachydactyly		HP:0000006	OMIM:120400	IEA					I	HPO:iea[2009-02-17]
OMIM:120400	Coloboma of macula with type B brachydactyly		HP:0000589	OMIM:120400	TAS					P	HPO:probinson[2009-02-17]
OMIM:120400	Coloboma of macula with type B brachydactyly		HP:0000104	OMIM:120400	TAS					P	HPO:probinson[2009-02-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000483	OMIM:610954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000486	PMID:17436255;PMID:17436254	PCS		6/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001212	PMID:17436255	PCS		2/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001250	PMID:17436254	PCS	HP:0011463	3/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001250	PMID:17436255	PCS	HP:0003621	2/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002066	OMIM:610954	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001252	PMID:17436255	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002020	PMID:17436254	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000280	PMID:17436254	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0011463	PMID:17436255	PCS		1/5			C	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000954	PMID:17436254	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001845	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0004879	PMID:17436255;PMID:17436254	PCS		9/10			P	HPO:probinson[2022-09-11];HPO:skoehler[2015-01-21];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001763	PMID:17436254	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002019	PMID:17436255;PMID:17436254	PCS		6/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002311	OMIM:610954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000054	PMID:17436254	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000252	PMID:17436255	PCS		4/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001344	PMID:17436255;PMID:17436254	PCS		9/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-11];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002079	PMID:17436255	PCS		3/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000293	OMIM:610954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000490	PMID:17436254	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001182	OMIM:610954	TAS					P	HPO:skoehler[2013-05-31]
OMIM:610954	Pitt-Hopkins syndrome		HP:0008081	OMIM:610954	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001217	PMID:17436254	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0025325	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000322	OMIM:610954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000960	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000006	PMID:17436254	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000687	PMID:17436254	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0004689	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000341	OMIM:610954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000582	OMIM:610954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001795	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002002	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001270	PMID:17436255	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000733	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002119	PMID:17436255	PCS		1/5			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0030084	OMIM:610954	TAS					P	HPO:skoehler[2014-09-21]
OMIM:610954	Pitt-Hopkins syndrome		HP:0001786	PMID:17436255	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000378	OMIM:610954	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002558	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000454	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0025517	PMID:17436255	PCS		3/5			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002236	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000154	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0003621	PMID:17436255	PCS		4/5			C	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000431	OMIM:610954	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610954	Pitt-Hopkins syndrome		HP:0004279	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0002650	PMID:17436255;PMID:17436254	PCS		3/10		HP:0012825	P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000194	PMID:17436255	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000391	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000470	OMIM:610954	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610954	Pitt-Hopkins syndrome		HP:0005484	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0011300	PMID:17436255	PCS		2/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0034250	PMID:17436254	PCS		1/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0100716	PMID:17436255	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0004704	PMID:17436255	PCS		2/6			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0200055	PMID:17436254	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000545	OMIM:610954	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610954	Pitt-Hopkins syndrome		HP:0000028	PMID:17436254	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:620897	Ovarian dysgenesis 11		HP:0003621	PMID:38105698	PCS		2/2			C	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0025708	PMID:34707299	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0010463	PMID:38105698	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0011969	PMID:38105698	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0008232	PMID:34707299;PMID:38105698	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0012569	PMID:34707299;PMID:38105698	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0000007	PMID:34707299	PCS					I	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0000823	PMID:34707299	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0008214	PMID:34707299	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0031103	PMID:38105698	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620897	Ovarian dysgenesis 11		HP:0000786	PMID:34707299;PMID:38105698	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0001891	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003453	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003454	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003496	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0001890	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003493	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002240	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0001904	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0001744	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002731	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002633	OMIM:601859	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002853	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0001880	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002730	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002851	OMIM:601859	TAS					P	HPO:probinson[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002972	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0001025	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003262	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003261	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002729	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0002923	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0001973	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003613	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0000006	OMIM:601859	IEA					I	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0003237	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:601859	Autoimmune lymphoproliferative syndrome		HP:0004844	OMIM:601859	IEA					P	HPO:iea[2009-02-17]
OMIM:613285	Deafness, autosomal recessive 25		HP:0003577	PMID:20137778	PCS		10/10			C	HPO:probinson[2024-03-14]
OMIM:613285	Deafness, autosomal recessive 25		HP:0000365	PMID:20137778	TAS		10/10			P	HPO:skoehler[2015-01-21];HPO:lccarmody[2018-10-04];HP:probinson[2019-01-03];HPO:probinson[2024-03-14]
OMIM:613285	Deafness, autosomal recessive 25		HP:0001751	PMID:20137778	PCS		0/4			P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-14]
OMIM:613285	Deafness, autosomal recessive 25		HP:0000408	PMID:20137778	TAS		3/10			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-14]
OMIM:613285	Deafness, autosomal recessive 25		HP:0000007	OMIM:613285	IEA					I	HPO:skoehler[2013-01-10]
OMIM:124100	Danubian endemic familial nephropathy		HP:0000112	OMIM:124100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217200	Convulsive disorder, familial, with prenatal or early onset		HP:0001250	OMIM:217200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217200	Convulsive disorder, familial, with prenatal or early onset		HP:0000007	OMIM:217200	IEA					I	HPO:iea[2009-02-17]
OMIM:217200	Convulsive disorder, familial, with prenatal or early onset		HP:0001522	OMIM:217200	IEA					C	HPO:iea[2009-02-17]
OMIM:217200	Convulsive disorder, familial, with prenatal or early onset		HP:0001249	OMIM:217200	IEA					P	HPO:iea[2009-02-17]
OMIM:217200	Convulsive disorder, familial, with prenatal or early onset		HP:0001336	OMIM:217200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001298	PMID:26912632	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001254	OMIM:615838	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003676	PMID:26912632	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001272	PMID:26912632	PCS		0/7			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0012707	PMID:26912632	PCS		3/4			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002283	PMID:24014394	PCS		1/1			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001251	PMID:26912632	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003593	PMID:26912632	PCS		2/6			C	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001290	PMID:24014394	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0033725	PMID:24014394	PCS		1/1			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0040081	PMID:26912632	PCS		0/4			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001508	PMID:26912632	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0000639	PMID:26912632	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001903	PMID:24014394	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0011463	PMID:24014394;PMID:26912632	PCS		2/7			C	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002518	PMID:26912632	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0007366	PMID:26912632	PCS		0/7			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002878	PMID:24014394	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001324	PMID:26912632	PCS		4/6			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001348	PMID:26912632	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001249	PMID:26912632	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0000577	PMID:26912632	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003348	PMID:26912632	PCS		2/7			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003128	PMID:24014394	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0008936	PMID:26912632	PCS		3/7			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002059	PMID:26912632	PCS		2/7			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003621	PMID:26912632	PCS		3/6			C	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003487	PMID:26912632	PCS		6/6			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002376	PMID:24014394;PMID:26912632	PCS		6/8			P	HPO:probinson[2022-09-22];HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001288	PMID:26912632	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0011924	PMID:26912632	PCS		3/6			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001260	PMID:26912632	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001263	PMID:26912632	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002151	PMID:24014394	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001285	PMID:24014394	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002490	PMID:26912632	PCS		2/2			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0045045	PMID:26912632	PCS		0/3			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003819	PMID:24014394	PCS		1/1			C	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0000508	PMID:26912632	PCS		2/7			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0000007	PMID:24014394	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0000505	PMID:26912632	PCS		5/7			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002505	PMID:24014394	PCS		1/1			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0000543	PMID:26912632	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001257	PMID:26912632	PCS		6/6			P	HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0002789	PMID:24014394	PCS		1/1			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0001259	PMID:24014394	PCS		1/1			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0000544	PMID:26912632	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:615838	Mitochondrial complex III deficiency, nuclear type 8		HP:0003678	OMIM:615838	TAS					C	HPO:skoehler[2015-12-30]
OMIM:251255	Jawad syndrome		HP:0003577	PMID:18071751	PCS		7/7			C	HPO:probinson[2022-08-06]
OMIM:251255	Jawad syndrome		HP:0000340	PMID:18071751	PCS	HP:0003577	7/7			P	HPO:probinson[2022-08-06]
OMIM:251255	Jawad syndrome		HP:0001263	PMID:21998596	PCS					P	HP:probinson[2019-03-02]
OMIM:251255	Jawad syndrome		HP:0004220	OMIM:251255	TAS					P	HPO:probinson[2009-02-17]
OMIM:251255	Jawad syndrome		HP:0004692	OMIM:251255	TAS					P	HPO:probinson[2009-02-17]
OMIM:251255	Jawad syndrome		HP:0005780	OMIM:251255	TAS					P	HPO:probinson[2009-02-17]
OMIM:251255	Jawad syndrome		HP:0100259	PMID:18071751	PCS					P	HPO:probinson[2022-08-06]
OMIM:251255	Jawad syndrome		HP:0000718	OMIM:251255	TAS					P	HPO:skoehler[2013-07-30]
OMIM:251255	Jawad syndrome		HP:0011451	PMID:18071751	PCS	HP:0003577	7/7			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-02];HPO:probinson[2022-08-06]
OMIM:251255	Jawad syndrome		HP:0000448	PMID:21998596	PCS					P	HPO:skoehler[2013-07-30];HP:probinson[2019-03-02]
OMIM:251255	Jawad syndrome		HP:0000007	PMID:21998596	PCS					I	HPO:probinson[2009-02-17];HP:probinson[2019-03-02]
OMIM:251255	Jawad syndrome		HP:0001822	OMIM:251255	TAS					P	HPO:probinson[2009-02-17]
OMIM:251255	Jawad syndrome		HP:0000278	OMIM:251255	TAS					P	HPO:skoehler[2013-07-30]
OMIM:251255	Jawad syndrome		HP:0002943	OMIM:251255	TAS					P	HPO:skoehler[2013-07-30]
OMIM:251255	Jawad syndrome		HP:0001249	PMID:18071751	PCS		7/7			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-02];HPO:probinson[2022-08-06]
OMIM:251255	Jawad syndrome		HP:0006216	OMIM:251255	TAS					P	HPO:probinson[2009-02-17]
OMIM:251255	Jawad syndrome		HP:0001798	PMID:18071751	PCS		7/7			P	HPO:probinson[2022-08-06]
OMIM:613291	Bile acid malabsorption, primary		HP:0002630	PMID:9109432	PCS		1/1			P	HPO:probinson[2013-02-19];HPO:probinson[2021-10-05]
OMIM:613291	Bile acid malabsorption, primary		HP:0034043	PMID:9109432	PCS		1/1			P	HPO:probinson[2022-02-03]
OMIM:613291	Bile acid malabsorption, primary		HP:0001508	OMIM:613291	TAS					P	HPO:skoehler[2013-06-23]
OMIM:613291	Bile acid malabsorption, primary		HP:0002570	PMID:9109432	PCS	HP:0003623	1/1			P	HPO:skoehler[2013-06-23];HPO:probinson[2021-10-05]
OMIM:613291	Bile acid malabsorption, primary		HP:0000007	PMID:9109432	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2021-10-05]
OMIM:613291	Bile acid malabsorption, primary		HP:0001510	OMIM:613291	TAS					P	HPO:skoehler[2013-06-23]
OMIM:613291	Bile acid malabsorption, primary		HP:0002028	PMID:9109432	PCS	HP:0003623	1/1			P	HPO:probinson[2013-02-19];HPO:probinson[2021-10-05]
OMIM:613291	Bile acid malabsorption, primary		HP:0003623	PMID:9109432	PCS		1/1			C	HPO:probinson[2021-10-05]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002463	PMID:4045952;PMID:11050011;PMID:34354969	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000486	PMID:22398176;PMID:4045952	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0004840	PMID:4045952;PMID:11050011	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0004322	PMID:11050011;PMID:34354969	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001250	PMID:34354969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001252	PMID:26242992;PMID:34354969	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001251	PMID:11118249;PMID:34354969	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0003593	PMID:4045952	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0012751	PMID:34354969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000716	PMID:26242992	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000639	PMID:11118249;PMID:26242992;PMID:11050011;PMID:34354969	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0011463	PMID:22398176;PMID:4045952;PMID:34354969	PCS		3/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000717	PMID:34354969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001924	PMID:4045952;PMID:11050011	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0020081	PMID:11118249;PMID:22398176	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0025373	PMID:34354969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0003487	PMID:4045952	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001260	PMID:11118249;PMID:22398176;PMID:26242992;PMID:4045952;PMID:11050011;PMID:34354969	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001263	PMID:11118249;PMID:26242992;PMID:4045952;PMID:11050011;PMID:34354969	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002470	PMID:26242992;PMID:4045952;PMID:11050011	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002075	PMID:11118249;PMID:4045952;PMID:11050011	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0100022	PMID:11118249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0012187	PMID:11118249;PMID:22398176;PMID:4045952;PMID:11050011	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001618	PMID:26242992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000726	PMID:11118249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001419	PMID:10196363	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000602	PMID:26242992	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001336	PMID:26242992	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0004447	PMID:22398176;PMID:4045952	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002169	PMID:4045952	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0003577	PMID:4045952;PMID:11050011	PCS		3/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001310	PMID:4045952	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000980	PMID:11050011	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001992	PMID:34354969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001272	PMID:11118249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002363	PMID:11118249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002080	PMID:4045952	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0012132	PMID:4045952	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0100543	PMID:11050011	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001903	PMID:11118249;PMID:4045952;PMID:34354969	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001824	PMID:11050011;PMID:34354969	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0006897	PMID:11118249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001347	PMID:11118249;PMID:4045952	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0034280	PMID:11118249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0006999	PMID:34354969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001321	PMID:26242992;PMID:11050011	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001288	PMID:11118249;PMID:22398176;PMID:4045952;PMID:34354969	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002172	PMID:11118249;PMID:22398176;PMID:26242992;PMID:34354969	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0011273	PMID:11118249;PMID:22398176;PMID:4045952	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0100753	PMID:11118249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0031020	PMID:4045952	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0032550	PMID:11118249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001511	PMID:4045952;PMID:11050011;PMID:34354969	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0002403	PMID:4045952	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0001315	PMID:11050011;PMID:34354969	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301310	Anemia, sideroblastic, and spinocerebellar ataxia		HP:0000028	PMID:34354969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0002850	OMIM:610798	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0006538	OMIM:610798	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0004322	OMIM:610798	TAS					P	HPO:probinson[2009-02-17]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0001010	OMIM:610798	TAS					P	HPO:probinson[2009-02-17]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0000007	OMIM:610798	TAS					I	HPO:probinson[2009-02-17]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0000280	OMIM:610798	TAS					P	HPO:probinson[2009-02-17]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0002721	OMIM:610798	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610798	Immunodeficiency due to defect in mapbp-interacting protein		HP:0001875	OMIM:610798	TAS					P	HPO:probinson[2012-07-25]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0100291	PMID:10775536	PCS					P	HPO:probinson[2010-09-07]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001272	PMID:33655933	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001250	PMID:10775536	PCS					P	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001251	PMID:10775536	PCS					P	HPO:probinson[2010-08-30]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:6001007	PMID:20301583	PCS					P	HPO:probinson[2024-08-04]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0010845	PMID:33655933	PCS		1/1			P	HPO:probinson[2010-09-07];HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0031290	OMIM:213700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000939	OMIM:213700	IEA					P	HPO:iea[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000518	PMID:10775536	PCS					P	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000738	OMIM:213700	TAS					P	HPO:probinson[2012-07-18]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0007340	PMID:33655933	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0007024	OMIM:213700	IEA					P	HPO:iea[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0002518	PMID:10775536	PCS					P	HPO:probinson[2010-09-07]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0025710	PMID:33655933	PCS		1/1			C	HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0003107	OMIM:213700	TAS					P	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001249	OMIM:213700	IEA					P	HPO:iea[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0002014	PMID:10775536	PCS					P	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0002059	PMID:33655933	PCS		1/1			P	HPO:probinson[2010-08-30];HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0003487	PMID:33655933	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001288	PMID:33655933	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000991	PMID:33655933	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001681	OMIM:213700	TAS					P	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0003482	PMID:10775536	PCS					P	HPO:probinson[2010-09-07]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001081	PMID:20301583	PCS					P	HPO:probinson[2010-09-07];HPO:probinson[2024-02-09]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0010874	PMID:10775536	PCS					P	HPO:probinson[2010-08-30]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:6000821	PMID:20301583	PCS					P	HPO:probinson[2024-08-04]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:6000203	PMID:33509302	PCS		2/2			P	HPO:probinson[2024-02-09]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0002093	OMIM:213700	IEA					P	HPO:iea[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0100321	PMID:10775536	PCS					P	HPO:probinson[2010-09-07]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0011448	PMID:33655933	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000726	PMID:10775536	PCS					P	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001658	OMIM:213700	IEA					P	HPO:iea[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0009830	PMID:10775536	PCS					P	HPO:probinson[2010-08-30]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0007256	PMID:10775536	PCS					P	HPO:probinson[2010-09-07]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000007	OMIM:213700	TAS					I	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000746	OMIM:213700	TAS					P	HPO:probinson[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0000543	PMID:11804206	PCS					P	HPO:probinson[2010-09-07]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001257	OMIM:213700	IEA					P	HPO:iea[2009-02-17]
OMIM:213700	Cerebrotendinous xanthomatosis		HP:0001114	OMIM:213700	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-02-09]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002069	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0008936	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002521	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001344	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010819	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0032792	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001263	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0003593	PMID:31678406	PCS		1/1			C	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010841	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0032794	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000006	PMID:31678406	PCS					I	HPO:probinson[2022-08-20]
OMIM:619964	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012469	PMID:31678406	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0002366	OMIM:614298	TAS	HP:0003584				P	HPO:skoehler[2013-07-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0003236	OMIM:614298	TAS				HP:0012825	P	HPO:skoehler[2014-01-28]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0003676	OMIM:614298	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001332	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001272	OMIM:614298	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0003693	OMIM:614298	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0003691	OMIM:614298	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001251	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0002460	OMIM:614298	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0002180	PMID:21981780	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0012048	PMID:21981780	PCS		10/24			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000716	OMIM:614298	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0011463	PMID:21981780	PCS		3/24			C	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0011462	PMID:21981780	PCS		2/24			C	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000712	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0007002	PMID:21981780	PCS		8/18			P	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0007325	PMID:21981780	PCS		15/23			P	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001268	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001347	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001265	OMIM:614298	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0002454	PMID:21981780	PCS		1/24			P	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0003621	PMID:21981780	PCS		19/24			C	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000750	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001300	PMID:21981780	PCS		13/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0003487	PMID:21981780	PCS		14/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001288	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001761	OMIM:614298	TAS					P	HPO:skoehler[2014-01-28]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001260	PMID:21981780	PCS		17/24			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001263	OMIM:614298	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0002071	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0100710	PMID:21981780	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0100315	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000529	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000726	OMIM:614298	TAS					P	HPO:skoehler[2013-07-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000007	PMID:21981780	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0007256	PMID:21981780	PCS		18/24			P	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000648	PMID:21981780	PCS		20/23			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0002505	PMID:21981780	PCS	HP:0011462	8/24			P	HPO:probinson[2022-05-26]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001257	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0000006	OMIM:614298	IEA					I	HPO:skoehler[2019-09-07]
OMIM:614298	Neurodegeneration with brain iron accumulation 4		HP:0001337	OMIM:614298	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604060	Deafness, autosomal recessive 20		HP:0000365	OMIM:604060	IEA	HP:0003593				P	HPO:skoehler[2013-01-09]
OMIM:604060	Deafness, autosomal recessive 20		HP:0000407	OMIM:604060	TAS					P	HPO:skoehler[2015-12-30]
OMIM:604060	Deafness, autosomal recessive 20		HP:0000007	OMIM:604060	TAS					I	HPO:skoehler[2015-12-30]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0002069	PMID:22424600	PCS		1/4			P	HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0002059	OMIM:226750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0002521	OMIM:226750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0000252	PMID:22424600	PCS		1/4		HP:0012825	P	HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0000750	PMID:22424600	PCS		4/4			P	HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0001321	OMIM:226750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0002376	PMID:22424600	PCS		3/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0031936	PMID:22424600	PCS		4/4			P	HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0001250	PMID:22424600	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0001263	OMIM:226750	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0001251	OMIM:226750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0032794	PMID:22424600	PCS		1/4			P	HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0000705	OMIM:226750	IEA					P	HPO:iea[2009-02-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0000726	OMIM:226750	IEA					P	HPO:iea[2009-02-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0006297	PMID:22424600	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0000007	PMID:22424600	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0200134	OMIM:226750	TAS					P	HPO:skoehler[2013-06-11]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0002119	OMIM:226750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0001257	OMIM:226750	IEA					P	HPO:iea[2009-02-17]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0007359	PMID:22424600	PCS		1/4			P	HPO:probinson[2023-03-23]
OMIM:226750	Kohlschutter-Tonz syndrome		HP:0001249	OMIM:226750	IEA					P	HPO:iea[2009-02-17]
OMIM:618449	Ciliary dyskinesia, primary, 41		HP:0031603	PMID:30665704	PCS					P	HPO:probinson[2019-07-07]
OMIM:618449	Ciliary dyskinesia, primary, 41		HP:0002110	PMID:30665704	PCS					P	HPO:probinson[2019-07-07]
OMIM:618449	Ciliary dyskinesia, primary, 41		HP:0000789	OMIM:618449	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618449	Ciliary dyskinesia, primary, 41		HP:0000007	PMID:30665704	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618449	Ciliary dyskinesia, primary, 41		HP:0000403	PMID:30665704	IEA					P	HPO:probinson[2019-07-07]
OMIM:618449	Ciliary dyskinesia, primary, 41		HP:0012208	PMID:30665704	IEA			MALE		P	HPO:probinson[2019-07-07]
OMIM:618449	Ciliary dyskinesia, primary, 41		HP:0011108	PMID:30665704	PCS					P	HPO:probinson[2019-07-07]
OMIM:610015	Glutamine deficiency, congenital		HP:0001298	PMID:21353613	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0002983	PMID:16267323	PCS	HP:0030674	1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0000463	PMID:16267323	PCS		1/2			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0001250	PMID:25970099;PMID:21353613	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0001371	PMID:25970099	PCS	HP:0003577	1/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0030674	PMID:21353613	IEA					C	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0003196	PMID:16267323	PCS		1/2			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0001252	PMID:16267323	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0001290	PMID:21353613	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0010783	PMID:16267323	PCS		1/2			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0012444	PMID:21353613	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0500147	PMID:16267323	PCS		2/2			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0001987	PMID:21353613	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0002416	PMID:16267323	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0003429	PMID:21353613	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0006956	PMID:16267323	PCS	HP:0030674	1/2			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0000431	PMID:16267323	TAS	HP:0003577	1/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0000233	PMID:16267323	PCS		1/2			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0002079	PMID:21353613	TAS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0001662	PMID:21353613	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0002395	PMID:21353613	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0011344	PMID:21353613	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0005280	PMID:16267323	PCS	HP:0003577	1/2			P	HPO:skoehler[2012-11-26];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0012385	PMID:16267323	PCS	HP:0003577	1/2			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0000007	PMID:16267323	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0002205	PMID:21353613	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0003811	PMID:16267323	PCS		2/2			C	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0500198	PMID:16267323;PMID:21353613	PCS		3/3			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0002643	PMID:16267323	PCS	HP:0003623	2/2			P	HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0000369	PMID:25970099	PCS	HP:0003577	2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610015	Glutamine deficiency, congenital		HP:0002104	PMID:21353613	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0001639	PMID:17273968	PCS					P	HPO:probinson[2013-04-01]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0001252	PMID:17273968	PCS					P	HPO:probinson[2013-04-01]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0012087	PMID:17273968	PCS					P	HPO:probinson[2013-04-01]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0000007	PMID:17273968	PCS					I	HPO:probinson[2013-04-01]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0002093	PMID:17273968	PCS					P	HPO:probinson[2013-04-01]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0000961	PMID:17273968	PCS	HP:0003623				P	HPO:probinson[2013-01-09]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0001942	PMID:17273968	PCS	HP:0003623				P	HPO:probinson[2013-04-01]
OMIM:610773	Mitochondrial phosphate carrier deficiency		HP:0003128	PMID:17273968	PCS	HP:0003623				P	HPO:probinson[2013-04-01]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0001344	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0002188	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0001250	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0001263	PMID:30221345	PCS	HP:0003593	2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0003593	PMID:30221345	PCS		2/2			C	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0000280	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0012469	PMID:30221345	PCS	HP:0003593	2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0000718	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0000717	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0000739	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0000007	PMID:30221345	TAS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0100716	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0000752	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619031	Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies		HP:0000303	PMID:30221345	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:609222	Dandy-Walker malformation with occipital cephalocele, autosomal dominant		HP:0004488	OMIM:609222	TAS					P	HPO:probinson[2009-02-17]
OMIM:609222	Dandy-Walker malformation with occipital cephalocele, autosomal dominant		HP:0003829	OMIM:609222	TAS					I	HPO:probinson[2009-02-17]
OMIM:609222	Dandy-Walker malformation with occipital cephalocele, autosomal dominant		HP:0001305	OMIM:609222	TAS					P	HPO:probinson[2009-02-17]
OMIM:609222	Dandy-Walker malformation with occipital cephalocele, autosomal dominant		HP:0004470	OMIM:609222	TAS					P	HPO:probinson[2012-07-16]
OMIM:609222	Dandy-Walker malformation with occipital cephalocele, autosomal dominant		HP:0000006	OMIM:609222	TAS					I	HPO:probinson[2009-02-17]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002069	PMID:18469812	PCS		2/5			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002521	OMIM:612164	PCS					P	HPO:probinson[2012-04-11]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002188	PMID:18469812	PCS		2/5			P	HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002123	OMIM:612164	PCS					P	HPO:probinson[2012-04-11]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0001151	OMIM:612164	PCS					P	HPO:probinson[2012-04-11]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0001252	OMIM:612164;PMID:18469812	PCS		12/15			P	HPO:probinson[2022-12-13];HPO:skoehler[2014-11-26]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0006808	OMIM:612164	PCS					P	HPO:probinson[2012-04-11]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0003593	PMID:18469812	PCS		4/5			C	HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0007105	OMIM:612164	PCS					P	HPO:probinson[2012-04-11]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0003623	PMID:18469812	PCS		1/5			C	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002059	PMID:18469812	PCS		4/5			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002510	PMID:18469812	PCS		4/5			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0001344	PMID:18469812	PCS		2/5			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002133	OMIM:612164	TAS					P	HPO:skoehler[2014-10-06]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002376	OMIM:612164	TAS					P	HPO:skoehler[2014-10-06]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0002079	PMID:18469812	PCS		1/5			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0001266	PMID:18469812	PCS		1/5			P	HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0010818	OMIM:612164	PCS					P	HPO:probinson[2012-04-11]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0010851	PMID:18469812	PCS		5/5			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0011344	PMID:18469812	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0011097	PMID:18469812	PCS		4/5			P	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0200134	PMID:18469812	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0001258	OMIM:612164	PCS					P	HPO:probinson[2012-04-11]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0000006	PMID:18469812	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-12-13]
OMIM:612164	Developmental and epileptic encephalopathy 4		HP:0001337	OMIM:612164	TAS					P	HPO:skoehler[2013-05-03]
OMIM:221995	Nephrogenic diabetes insipidus - intracranial calcification		HP:0003510	OMIM:221995	TAS					P	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:221995	Nephrogenic diabetes insipidus - intracranial calcification		HP:0009806	OMIM:221995	TAS					P	HPO:skoehler[2015-01-27]
OMIM:221995	Nephrogenic diabetes insipidus - intracranial calcification		HP:0001263	OMIM:221995	TAS					P	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:221995	Nephrogenic diabetes insipidus - intracranial calcification		HP:0002514	OMIM:221995	TAS					P	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001650	PMID:34570759	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000486	PMID:34570759	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0002263	PMID:34570759	PCS		35/35			P	HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001250	PMID:22279524;PMID:34570759	PCS		37/37			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001252	PMID:34570759	PCS		35/35			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0012802	PMID:22279524	PCS		2/2			P	HPO:skoehler[2014-06-24]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001607	OMIM:614501	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001647	PMID:34570759	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000414	PMID:22279524	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001943	PMID:34570759	PCS		7/35			P	HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0002119	PMID:22279524	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0003429	PMID:22279524	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000218	PMID:34570759	PCS		35/35			P	HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000158	OMIM:614501	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001601	PMID:34570759	PCS		26/35			P	HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001265	PMID:34570759	PCS		35/35			P	HPO:skoehler[2012-10-17]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000154	PMID:22279524;PMID:34570759	PCS		37/37			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0002353	PMID:34570759	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0004279	PMID:34570759	PCS		18/35			P	HPO:skoehler[2012-10-17]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001762	PMID:34570759	PCS		5/35			P	HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0002079	PMID:22279524	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0011968	PMID:34570759	PCS	HP:0003623	35/35			P	HPO:skoehler[2012-11-20]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001182	PMID:22279524;PMID:34570759	PCS		20/37			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0011344	PMID:22279524;PMID:34570759	PCS		37/37			P	HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0011304	PMID:22279524	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001518	PMID:34570759	PCS		18/35			P	HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0001537	PMID:34570759	PCS		7/35			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000007	PMID:22279524	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0002500	PMID:34570759	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000666	PMID:34570759	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614501	Psychomotor retardation, epilepsy, and craniofacial dysmorphism		HP:0000347	PMID:34570759	PCS		10/35			P	HPO:probinson[2023-03-04]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0002015	PMID:23836506	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0000252	PMID:23836506	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0001264	OMIM:617008	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0002510	OMIM:617008	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0000486	OMIM:617008	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0000750	PMID:23836506	PCS		2/4			P	HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0001250	PMID:23836506	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0001260	PMID:23836506	PCS		1/4			P	HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0001263	PMID:23836506	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0003593	PMID:23836506	PCS		3/3			C	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0002282	PMID:23836506	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0100543	OMIM:617008	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0000639	OMIM:617008	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0000605	OMIM:617008	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0003828	OMIM:617008	TAS					M	HPO:skoehler[2017-07-13]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0007256	PMID:23836506	TAS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0000007	PMID:23836506	TAS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0025711	PMID:23836506	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0001257	PMID:23836506	PCS		4/4			P	HPO:probinson[2021-09-20]
OMIM:617008	Cerebral palsy, spastic quadriplegic, 3		HP:0000577	PMID:23836506	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-20]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0032989	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0002421	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0001385	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0000252	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0002015	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0031936	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0004322	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0001263	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0003593	PMID:31039582	PCS		1/1			C	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0001270	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0033128	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0000007	PMID:31039582	PCS					I	HPO:probinson[2020-11-30];HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0001338	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0000846	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0008347	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0001511	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0007325	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619025	Combined oxidative phosphorylation deficiency 50		HP:0001348	PMID:31039582	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0002751	PMID:24334604	PCS		1/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0010628	PMID:24334604	PCS		1/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0001371	PMID:24334604	PCS		3/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0001382	PMID:24334604	PCS		3/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0001284	PMID:24334604	PCS		2/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0003560	PMID:24334604	PCS					P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0003593	PMID:24334604	PCS		1/3			C	HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0001270	PMID:24334604	PCS		3/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0000007	PMID:24334604	PCS					I	HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0001319	PMID:24334604	PCS	HP:0003623	2/3			P	HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0000218	PMID:24334604	PCS		2/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0002877	PMID:24334604	PCS		1/3			P	HPO:probinson[2021-02-28];HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0000006	PMID:24334604	PCS					I	HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0003623	PMID:24334604	IEA		2/3			C	HPO:probinson[2021-02-28]
OMIM:616470	Ullrich congenital muscular dystrophy 2		HP:0003557	PMID:24334604	PCS		3/3			P	HPO:probinson[2021-02-28]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000286	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0003236	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000486	PMID:33602924	PCS		2/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0003596	PMID:33602924	PCS		2/8			C	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0004322	PMID:33602924	PCS		4/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0003198	PMID:33602924	PCS		3/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0012707	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001252	PMID:33602924	PCS		4/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0003593	PMID:33602924	IEA		2/8			C	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0012625	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0010602	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0033725	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0011342	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0011463	PMID:33602924	PCS		3/8			C	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0011462	PMID:33602924	PCS		1/8			C	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000954	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0004912	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001324	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0003701	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000114	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001488	PMID:33602924	PCS		2/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0002019	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001249	PMID:33602924	PCS		3/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0003202	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000252	PMID:33602924	PCS		2/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001344	PMID:33602924	PCS		2/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0005101	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001263	PMID:33602924	PCS		3/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0002151	PMID:33602924	PCS		2/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000805	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000007	PMID:33602924	PCS					I	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000601	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0007359	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000006	PMID:33602924	PCS					I	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0002148	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000463	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001992	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0012408	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0002917	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001903	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0002119	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000218	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000577	PMID:33602924	PCS		2/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000750	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001762	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0002970	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000194	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000590	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0000592	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0011344	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0005280	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0008180	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001994	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:619743	Combined oxidative phosphorylation deficiency 55		HP:0001873	PMID:33602924	PCS		1/8			P	HPO:probinson[2022-04-19]
OMIM:188201	Thumbs, stiff, with brachydactyly type A1 and developmental delay		HP:0009371	OMIM:188201	TAS					P	HPO:skoehler[2009-02-17]
OMIM:188201	Thumbs, stiff, with brachydactyly type A1 and developmental delay		HP:0001263	OMIM:188201	IEA					P	HPO:skoehler[2015-12-30]
OMIM:188201	Thumbs, stiff, with brachydactyly type A1 and developmental delay		HP:0000006	OMIM:188201	TAS					I	HPO:skoehler[2009-02-17]
OMIM:188201	Thumbs, stiff, with brachydactyly type A1 and developmental delay		HP:0001249	OMIM:188201	TAS					P	HPO:skoehler[2009-02-17]
OMIM:162800	Cyclic neutropenia		HP:0040289	PMID:10581030	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:162800	Cyclic neutropenia		HP:0000155	PMID:10581030	PCS					P	HPO:probinson[2023-02-12]
OMIM:162800	Cyclic neutropenia		HP:0001945	PMID:10581030	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-12]
OMIM:162800	Cyclic neutropenia		HP:0000006	PMID:10581030	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:162800	Cyclic neutropenia		HP:0033834	PMID:10581030	PCS					P	HPO:probinson[2023-02-12]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0001022	PMID:23395477	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-20]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0000639	PMID:23395477	PCS		9/9			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-03-20]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0012805	PMID:23395477	PCS		9/9			P	HPO:probinson[2023-03-20]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0000613	OMIM:615179	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0008499	PMID:23395477	PCS		4/9			P	HPO:probinson[2023-03-20]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0000007	PMID:23395477	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2023-03-20]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0007663	PMID:23395477	PCS		9/9			P	HPO:probinson[2023-03-20]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0000565	PMID:23395477	PCS		2/9			P	HPO:probinson[2023-03-20]
OMIM:615179	Albinism, oculocutaneous, type V		HP:0000577	PMID:23395477	PCS		1/9			P	HPO:probinson[2023-03-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0006989	PMID:26571461;PMID:27329731	PCS		2/4			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0011819	PMID:26571461	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000486	PMID:26571461	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001250	PMID:26571461	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000160	PMID:26571461	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001252	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001251	PMID:27329731	PCS		1/1			P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002020	PMID:26571461	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0004482	PMID:27550220	PCS		2/3			P	HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001290	PMID:27329731	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0011342	PMID:27329731	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000718	PMID:27329731	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000717	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000678	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001643	PMID:27550220	PCS	HP:0003623	2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001763	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001249	PMID:27550220;PMID:27329731	PCS		11/11			P	HPO:probinson[2017-06-17];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002751	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0004411	PMID:26571461	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0030223	PMID:27329731	PCS		1/1			P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001382	PMID:27329731	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001263	PMID:27550220;PMID:27329731	PCS		11/11			P	HPO:probinson[2017-06-17];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0040194	PMID:27329731	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0007074	PMID:26571461	PCS		2/3			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001419	PMID:27550220	PCS					I	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0011098	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000448	PMID:27329731	TAS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002705	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002307	PMID:26571461	PCS		3/3			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001533	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000322	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001337	PMID:27329731	PCS		1/1			P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000446	PMID:26571461	PCS		3/3			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000687	PMID:27550220	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001655	PMID:27550220	PCS	HP:0003623	1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001611	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000582	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002684	PMID:27329731	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001270	PMID:27329731	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001629	PMID:27550220	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0009640	PMID:26571461	PCS		3/3			P	HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001822	PMID:27329731	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000256	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001667	PMID:27550220	PCS	HP:0003623	1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000154	PMID:27329731	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0008936	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002650	PMID:26571461	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000750	PMID:26571461	PCS		3/3			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000276	PMID:26571461;PMID:27329731	PCS		4/4			P	HPO:probinson[2021-02-20];HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0031936	PMID:26571461;PMID:27329731	PCS		4/4			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001640	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001321	PMID:26571461	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000194	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0030682	PMID:27550220	PCS					P	HPO:probinson[2017-06-17]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000272	PMID:26571461	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0011664	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0032988	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0100710	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0012683	PMID:27329731	PCS		1/1			P	HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002808	PMID:26571461	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001319	PMID:26571461	PCS	HP:0003623	2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000823	PMID:26571461	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0002007	PMID:27550220	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0001631	PMID:27550220	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000545	PMID:26571461	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:300967	Intellectual developmental disorder, X-linked syndromic 34		HP:0000028	PMID:26571461	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:167950	Papillomatosis, florid, of nipple		HP:0000006	OMIM:167950	IEA					I	HPO:iea[2009-02-17]
OMIM:167950	Papillomatosis, florid, of nipple		HP:0000951	OMIM:167950	IEA					P	HPO:iea[2009-02-17]
OMIM:618475	Paragangliomas 7		HP:0003581	PMID:30929736	PCS		8/8			C	HPO:probinson[2022-12-22]
OMIM:618475	Paragangliomas 7		HP:0003829	PMID:30929736	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-22]
OMIM:618475	Paragangliomas 7		HP:0002668	PMID:30929736	PCS		6/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-22]
OMIM:618475	Paragangliomas 7		HP:0000006	PMID:30929736	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-22]
OMIM:618475	Paragangliomas 7		HP:0002666	PMID:30929736	PCS		3/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-22]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0001540	PMID:27476657	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0000572	PMID:27476657	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0003676	PMID:27476657	PCS					C	HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0003155	PMID:27476657	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0410276	PMID:27476657	PCS		8/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:4000093	PMID:27476657	PCS		8/8			P	HPO:probinson[2023-01-27]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0001537	PMID:27476657	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0000007	PMID:27476657	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0002516	PMID:27476657	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0000520	PMID:27476657	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0001931	PMID:27476657	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0000324	PMID:27476657	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:606893	Vascular malformation, primary intraosseous		HP:0000225	PMID:27476657	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000365	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0002023	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000160	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0005650	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0002020	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000316	PMID:28369379	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0100807	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000636	PMID:28369379	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001643	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0009901	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0005469	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000453	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0010715	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0002230	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001263	PMID:28369379	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000294	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0011800	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0009099	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000322	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0008689	PMID:28369379	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000369	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000248	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000006	PMID:28369379	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001655	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001776	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000220	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001792	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0003577	PMID:28369379	PCS		2/2			C	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000260	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0002000	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0010709	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0009882	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0008551	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001746	PMID:28369379	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0009765	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000218	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000774	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000378	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000455	PMID:28369379	PCS		2/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000894	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000396	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001561	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000431	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000750	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000475	PMID:28369379	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000430	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0001321	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0005487	PMID:28369379	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0009909	PMID:28369379	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000349	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617746	Sweeney-Cox syndrome		HP:0000347	PMID:28369379	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:267730	Reticulum cell sarcoma		HP:0002664	OMIM:267730	IEA					P	HPO:iea[2009-02-17]
OMIM:267730	Reticulum cell sarcoma		HP:0000007	OMIM:267730	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:267730	Reticulum cell sarcoma		HP:0100242	OMIM:267730	IEA					P	HPO:skoehler[2015-01-27]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0003621	PMID:14567970	PCS		1/1			C	HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0031318	PMID:17097056	PCS		1/2			P	HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0031319	PMID:17097056	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0001695	OMIM:612158	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0005110	OMIM:612158	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0030682	OMIM:612158	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0011421	PMID:14567970	PCS		1/1			C	HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0001706	PMID:14567970	PCS		1/1			P	HPO:probinson[2013-04-04];HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0001639	PMID:17097056	PCS		3/3			P	HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0011462	PMID:17097056	PCS		3/3			C	HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0001712	OMIM:612158	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0006685	PMID:17097056	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0000006	PMID:14567970	PCS					I	HPO:probinson[2013-04-04]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0001678	OMIM:612158	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0001644	PMID:14567970	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2022-07-03]
OMIM:612158	Cardiomyopathy, dilated, 1AA, with or without LVNC		HP:0004755	OMIM:612158	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0002069	PMID:24239382	PCS		3/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0030799	PMID:24239382	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0001212	PMID:24239382	PCS		2/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0002121	PMID:24239382	PCS		2/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0001252	PMID:24239382	PCS		6/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0002240	PMID:24239382	PCS		1/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0001270	PMID:25847626	PCS		1/2			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0011463	PMID:25847626	IEA		1/2			C	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0011220	PMID:25847626	PCS		2/2			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000739	PMID:25847626;PMID:24239382	PCS		9/11			P	HPO:probinson[2022-06-16];HPO:skoehler[2014-03-24];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000316	PMID:24239382	PCS		2/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000733	PMID:25847626;PMID:24239382	PCS		6/11			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-06-16];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0002119	PMID:24239382	PCS		1/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000218	PMID:25847626	PCS		2/2			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0006532	PMID:24239382	PCS		2/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000455	OMIM:615637	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000256	PMID:25847626;PMID:24239382	PCS		9/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-16];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000278	PMID:25847626	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0001249	PMID:25847626;PMID:24239382	PCS		10/11			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-06-16];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0001744	PMID:24239382	PCS		2/9			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000494	OMIM:615637	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0003621	PMID:25847626	PCS		1/2			C	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000750	PMID:25847626;PMID:24239382	PCS		10/11			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0002197	PMID:25847626	PCS		1/2			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0001263	PMID:25847626	PCS		1/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000729	PMID:25847626	PCS		1/2			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000007	PMID:24239382	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0100716	PMID:25847626	PCS		1/2			P	HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0004209	PMID:24239382	PCS		3/9			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000268	OMIM:615637	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0002007	PMID:24239382	PCS		9/9			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-06-16]
OMIM:615637	Intellectual developmental disorder, autosomal recessive 41		HP:0000303	PMID:24239382	PCS		5/9			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-06-16]
OMIM:114000	Caffey disease		HP:0002982	OMIM:114000	TAS					P	HPO:probinson[2012-07-16]
OMIM:114000	Caffey disease		HP:0005731	OMIM:114000	TAS					P	HPO:probinson[2012-08-03]
OMIM:114000	Caffey disease		HP:0001382	PMID:15864348	PCS					P	HPO:probinson[2022-04-23]
OMIM:114000	Caffey disease		HP:0031485	PMID:15864348	PCS		3/3			P	HPO:probinson[2022-04-23]
OMIM:114000	Caffey disease		HP:6000811	PMID:24390061	PCS					P	HPO:probinson[2024-08-03]
OMIM:114000	Caffey disease		HP:0004490	OMIM:114000	TAS	HP:0003593				P	HPO:probinson[2012-07-30]
OMIM:114000	Caffey disease		HP:6000936	PMID:24390061	PCS					P	HPO:probinson[2024-08-03]
OMIM:114000	Caffey disease		HP:6000812	PMID:24390061	PCS					P	HPO:probinson[2024-08-03]
OMIM:114000	Caffey disease		HP:6000937	PMID:24390061	PCS					P	HPO:probinson[2024-08-03]
OMIM:114000	Caffey disease		HP:6000809	PMID:21249479	PCS					P	HPO:probinson[2024-08-03]
OMIM:114000	Caffey disease		HP:0002979	OMIM:114000	TAS	HP:0003577			HP:0012825	P	HPO:probinson[2012-07-30]
OMIM:114000	Caffey disease		HP:0006465	PMID:15864348	PCS	HP:0003593	3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-23]
OMIM:114000	Caffey disease		HP:0001945	OMIM:114000	TAS					P	HPO:probinson[2009-02-17]
OMIM:114000	Caffey disease		HP:0000006	PMID:15864348	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-04-23]
OMIM:190300	Tremor, hereditary essential, 1		HP:0003676	OMIM:190300	IEA					C	HPO:iea[2009-02-17]
OMIM:190300	Tremor, hereditary essential, 1		HP:0002345	OMIM:190300	TAS					P	HPO:probinson[2013-04-02]
OMIM:190300	Tremor, hereditary essential, 1		HP:0002378	OMIM:190300	TAS					P	HPO:probinson[2013-04-02]
OMIM:190300	Tremor, hereditary essential, 1		HP:0001260	OMIM:190300	TAS					P	HPO:probinson[2009-02-17]
OMIM:190300	Tremor, hereditary essential, 1		HP:0002174	OMIM:190300	TAS					P	HPO:probinson[2013-04-02]
OMIM:190300	Tremor, hereditary essential, 1		HP:0000006	OMIM:190300	IEA					I	HPO:iea[2009-02-17]
OMIM:618313	Diamond-Blackfan anemia 20		HP:0012133	PMID:27909223	PCS					P	HPO:probinson[2019-06-13]
OMIM:618313	Diamond-Blackfan anemia 20		HP:0008807	PMID:27909223	PCS		1/3			P	HPO:probinson[2019-06-13]
OMIM:618313	Diamond-Blackfan anemia 20		HP:0001903	PMID:27909223	PCS	HP:0003593	3/3			P	HPO:probinson[2019-06-13]
OMIM:618313	Diamond-Blackfan anemia 20		HP:0005160	PMID:27909223	PCS	HP:0003577	1/3			P	HPO:probinson[2019-06-13]
OMIM:618313	Diamond-Blackfan anemia 20		HP:0000006	PMID:27909223	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0008936	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0002521	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0002133	PMID:27270415	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0002376	PMID:25558065	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0001332	PMID:27270415	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0002033	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0001251	PMID:25558065	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0002020	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0003593	PMID:27270415;PMID:25558065	PCS		4/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0012736	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0000737	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0002509	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0031165	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0008499	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0000007	PMID:25558065	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0200134	PMID:25558065	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0002835	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0007843	PMID:27270415	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:617020	Epileptic encephalopathy, early infantile, 38		HP:0000556	PMID:27270415	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:262890	Scott syndrome		HP:0001892	OMIM:262890	TAS					P	HPO:skoehler[2013-03-15]
OMIM:262890	Scott syndrome		HP:0008354	OMIM:262890	TAS					P	HPO:probinson[2009-02-17]
OMIM:262890	Scott syndrome		HP:0000007	OMIM:262890	TAS					I	HPO:probinson[2009-02-17]
OMIM:611451	Deafness, autosomal recessive 63		HP:0003577	PMID:17211611	PCS		8/8			C	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-14]
OMIM:611451	Deafness, autosomal recessive 63		HP:0001751	PMID:17211611	PCS		0/4			P	HPO:probinson[2017-06-17];HPO:probinson[2024-03-14]
OMIM:611451	Deafness, autosomal recessive 63		HP:0001098	PMID:18953341	PCS		0/4			P	HPO:probinson[2024-03-14]
OMIM:611451	Deafness, autosomal recessive 63		HP:0000007	PMID:18794526	PCS					I	HPO:probinson[2017-06-17]
OMIM:611451	Deafness, autosomal recessive 63		HP:0008527	PMID:18794526	PCS	HP:0003577				P	HPO:probinson[2017-06-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0002345	PMID:38527963	PCS		4/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0003236	PMID:38527963	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0002064	PMID:38527963	PCS		8/8			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0002061	PMID:38527963	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0012548	PMID:38527963	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001270	PMID:38527963	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0011463	PMID:38527963	PCS		9/13			C	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0009027	PMID:38527963	PCS		11/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0007002	PMID:38527963	PCS		11/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0003307	PMID:38527963	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0002359	PMID:38527963	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0007149	PMID:38527963	PCS		11/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001763	PMID:38527963	PCS		9/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001249	PMID:38527963	PCS		0/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001347	PMID:38527963	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001765	PMID:38527963	PCS		6/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0003621	PMID:38527963	PCS		4/13			C	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001288	PMID:38527963	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0008959	PMID:38527963	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0000012	PMID:38527963	PCS		2/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0003487	PMID:38527963	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001761	PMID:38527963	PCS		4/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0031936	PMID:38527963	PCS		2/11			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0001283	PMID:38527963	PCS		0/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0009053	PMID:38527963	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0009077	PMID:38527963	PCS		10/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0000007	PMID:38527963	PCS					I	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0030051	PMID:38527963	PCS		8/8			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0003438	PMID:38527963	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620854	Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity		HP:0008944	PMID:38527963	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:119530	Orofacial cleft 1		HP:0000175	OMIM:119530	TAS					P	HPO:skoehler[2010-06-20]
OMIM:119530	Orofacial cleft 1		HP:0003577	OMIM:119530	TAS					C	HPO:probinson[2022-09-02]
OMIM:119530	Orofacial cleft 1		HP:0000006	OMIM:119530	TAS					I	HPO:probinson[2009-02-17]
OMIM:119530	Orofacial cleft 1		HP:0000204	OMIM:119530	TAS					P	HPO:probinson[2009-02-17]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0010280	PMID:22850876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-26]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0001041	PMID:22850876	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-26]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0011463	PMID:22850876	PCS		2/2			C	HPO:probinson[2023-01-26]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0002097	PMID:22850876	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-26]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0000007	PMID:22850876	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-26]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0032215	PMID:22850876	PCS		2/2			P	HPO:probinson[2023-01-26]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0030080	PMID:22850876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-26]
OMIM:618307	Epidermodysplasia verruciformis, susceptibility to, 4		HP:0031514	PMID:22850876	PCS		2/2			P	HPO:probinson[2023-01-26]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0001254	PMID:14742428	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0002179	PMID:2022752	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0010913	PMID:14742428	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0011968	PMID:2022752;PMID:14742428	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0001250	PMID:14742428	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0003593	PMID:14742428	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0000007	PMID:2022752	PCS					I	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0010911	PMID:2022752;PMID:14742428	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0010910	PMID:14742428	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620698	Maple syrup urine disease, type Ib		HP:0003623	PMID:2022752	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:620840	Premature ovarian failure 24		HP:0033085	PMID:32303603	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0000869	PMID:32303603	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0011969	PMID:32303603	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0008222	PMID:32303603	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0011462	PMID:32303603	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0008232	PMID:32303603	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0000876	PMID:32303603	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0000007	PMID:32303603	PCS					I	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0031103	PMID:32303603	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620840	Premature ovarian failure 24		HP:0008214	PMID:32303603	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003676	OMIM:603041	TAS					C	HPO:skoehler[2012-10-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002024	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002460	PMID:14757860;OMIM:603041	PCS		11/11			P	HPO:probinson[2022-05-18];HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0033842	PMID:10852545	PCS		14/15			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002936	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002579	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002019	OMIM:603041	TAS					P	HPO:skoehler[2013-01-22]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003548	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0000597	PMID:10852545	PCS		35/35			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0001249	PMID:10852545	PCS		1/35			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002578	PMID:10852545	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003200	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0000651	PMID:14757860	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002352	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0030143	PMID:10852545	PCS		24/25			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0012533	PMID:14757860	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0034276	PMID:14757860	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0000407	PMID:10852545	PCS		14/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0000726	PMID:10852545	PCS		0/35			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0100613	OMIM:603041	TAS					C	HPO:skoehler[2013-01-22]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0034277	PMID:14757860	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0000007	PMID:9924029	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0001533	OMIM:603041	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002027	PMID:10852545	PCS		17/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0004326	OMIM:603041	TAS					P	HPO:skoehler[2013-01-22]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0033748	PMID:14757860	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0004389	PMID:10852545	PCS		11/17			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:6000570	PMID:10852545	PCS		16/16			P	HPO:probinson[2024-04-03]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003693	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0031368	OMIM:603041	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0007141	PMID:14757860	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0007103	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0001824	PMID:10852545;PMID:14757860	PCS		20/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-18];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003688	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003128	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003689	PMID:14757860	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002014	PMID:10852545	PCS		27/29			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002015	PMID:10852545	PCS		12/28			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003621	PMID:14757860	PCS		1/1			C	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002254	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002013	PMID:10852545;PMID:14757860	PCS		24/32			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0000590	PMID:14757860;OMIM:603041	PCS		11/11			P	HPO:probinson[2022-05-18];HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002253	PMID:10852545	PCS		16/24			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0001284	PMID:10852545	PCS		27/33			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0004395	OMIM:603041	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0000508	PMID:10852545;PMID:14757860	PCS		35/35			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18];HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0032155	PMID:10852545	PCS		25/28			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0009830	PMID:10852545	PCS		34/34			P	HPO:probinson[2022-05-18]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0003737	OMIM:603041	IEA					P	HPO:iea[2009-02-17]
OMIM:603041	Mitochondrial DNA depletion syndrome 1 (MNGIE type)		HP:0002522	PMID:14757860	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:227300	Factor V and factor VIII, combined deficiency of		HP:0001892	OMIM:227300	IEA					P	HPO:iea[2009-02-17]
OMIM:227300	Factor V and factor VIII, combined deficiency of		HP:0003125	OMIM:227300	IEA					P	HPO:iea[2009-02-17]
OMIM:227300	Factor V and factor VIII, combined deficiency of		HP:0003225	OMIM:227300	IEA					P	HPO:iea[2009-02-17]
OMIM:227300	Factor V and factor VIII, combined deficiency of		HP:0000007	OMIM:227300	IEA					I	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0001385	OMIM:302802	IEA					P	HPO:skoehler[2019-04-18]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0003376	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0002650	OMIM:302802	IEA					P	HPO:skoehler[2019-04-18]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0001761	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0003693	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0003484	OMIM:302802	IEA					P	HPO:probinson[2012-03-13]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0002385	OMIM:302802	IEA					P	HPO:skoehler[2018-10-08]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0003482	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0001284	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0002460	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0001419	OMIM:302802	IEA					I	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0009027	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0002936	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:302802	Charcot-Marie-Tooth disease, X-linked recessive, 3		HP:0000762	OMIM:302802	IEA					P	HPO:iea[2009-02-17]
OMIM:613252	Cardiomyopathy, dilated, 1EE		HP:0003596	PMID:15998695	PCS		3/3			C	HPO:probinson[2022-07-04]
OMIM:613252	Cardiomyopathy, dilated, 1EE		HP:0001635	PMID:15998695	PCS		3/3			P	HPO:probinson[2022-07-04]
OMIM:613252	Cardiomyopathy, dilated, 1EE		HP:0012664	PMID:15998695	PCS		3/3			P	HPO:probinson[2022-07-04]
OMIM:613252	Cardiomyopathy, dilated, 1EE		HP:0033755	PMID:15998695	PCS		3/3			P	HPO:probinson[2022-07-04]
OMIM:613252	Cardiomyopathy, dilated, 1EE		HP:0000006	PMID:15998695	PCS					I	HPO:probinson[2022-07-04]
OMIM:613252	Cardiomyopathy, dilated, 1EE		HP:0001644	PMID:15998695	PCS		3/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-07-04]
DECIPHER:39	8p23.1 deletion syndrome		HP:0006695	DECIPHER:39	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:39	8p23.1 deletion syndrome		HP:0001627	DECIPHER:39	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:39	8p23.1 deletion syndrome		HP:0000752	DECIPHER:39	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:39	8p23.1 deletion syndrome		HP:0001631	DECIPHER:39	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:39	8p23.1 deletion syndrome		HP:0001249	DECIPHER:39	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:39	8p23.1 deletion syndrome		HP:0000028	DECIPHER:39	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:39	8p23.1 deletion syndrome		HP:0000776	DECIPHER:39	IEA					P	HPO:skoehler[2013-05-29]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0003577	PMID:22766609	PCS		2/2			C	HPO:probinson[2023-03-02]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000750	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000343	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000541	OMIM:615145	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0001263	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000482	PMID:22766609	PCS		2/2			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-02]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0045025	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0012043	OMIM:615145	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000508	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000316	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000007	PMID:22766609	PCS					I	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-02]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000612	PMID:22766609	PCS		2/2			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-02]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000568	PMID:22766609	PCS		2/2			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-02]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0007663	PMID:22766609	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-02]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000505	PMID:22766609	PCS		2/2			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-02]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000647	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000565	OMIM:615145	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000400	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0007700	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0001249	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0000369	OMIM:615145	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615145	Microphthalmia, isolated, with coloboma 9		HP:0001116	PMID:22766609	PCS		1/2			P	HPO:probinson[2023-03-02]
OMIM:617752	Clark-Baraitser syndrome		HP:0000286	PMID:27848077;PMID:28251352	PCS		4/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000582	OMIM:617752	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617752	Clark-Baraitser syndrome		HP:0000340	PMID:28251352	PCS		1/9			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000486	OMIM:617752	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617752	Clark-Baraitser syndrome		HP:0000343	PMID:27848077;PMID:28251352	PCS		2/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000463	PMID:27848077;PMID:28251352	PCS		2/16			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0001250	PMID:27848077;PMID:28251352	PCS		4/19			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0002263	PMID:27848077;PMID:28251352	PCS		4/16			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0003196	PMID:27848077;PMID:28251352	PCS		2/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0001252	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0001270	PMID:28251352	PCS		7/8			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000319	PMID:27848077	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000718	PMID:28251352	PCS		3/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000739	PMID:28251352	PCS		1/9			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000316	PMID:27848077;PMID:28251352	PCS		2/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000219	PMID:27848077;PMID:28251352	PCS		3/16			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0009765	PMID:27848077;PMID:28251352	PCS		4/16			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000218	OMIM:617752	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617752	Clark-Baraitser syndrome		HP:0002714	PMID:28251352	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0030084	OMIM:617752	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617752	Clark-Baraitser syndrome		HP:0000752	PMID:28251352	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0009748	PMID:27848077;PMID:28251352	PCS		6/16			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0001249	PMID:27479843;PMID:27848077;PMID:28251352	PCS		22/22			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000154	PMID:27848077;PMID:28251352	PCS		6/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000252	PMID:27848077;PMID:28251352	PCS		2/17			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000750	PMID:27479843;PMID:27848077;PMID:28251352	PCS		19/21			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0001263	PMID:27848077;PMID:28251352	PCS		20/20			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0045025	PMID:28251352	PCS		4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0005280	PMID:27848077;PMID:28251352	PCS		1/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000729	PMID:28251352	PCS		6/8			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000307	PMID:28251352	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0001852	OMIM:617752	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617752	Clark-Baraitser syndrome		HP:0000268	PMID:28251352	PCS		1/9			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000322	PMID:28251352	PCS		1/8			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0001513	PMID:27848077;PMID:28251352	PCS		6/18			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000369	PMID:27848077;PMID:28251352	PCS		3/16			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000248	PMID:28251352	PCS		1/9			P	HPO:probinson[2022-07-20]
OMIM:617752	Clark-Baraitser syndrome		HP:0000006	PMID:27479843	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-07-20]
OMIM:607541	Corneal dystrophy, Avellino type		HP:0003621	PMID:9727418	PCS		4/5			C	HPO:probinson[2023-02-09]
OMIM:607541	Corneal dystrophy, Avellino type		HP:0011463	PMID:9727418	PCS		1/5			C	HPO:probinson[2023-02-09]
OMIM:607541	Corneal dystrophy, Avellino type		HP:0007663	PMID:9727418	PCS		5/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-09]
OMIM:607541	Corneal dystrophy, Avellino type		HP:0000505	PMID:9727418	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-09]
OMIM:607541	Corneal dystrophy, Avellino type		HP:0000006	PMID:9054935	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-09]
OMIM:607541	Corneal dystrophy, Avellino type		HP:0001149	PMID:9727418	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-09]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003774	PMID:28392951	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003577	PMID:17413422	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000100	PMID:28392951	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003077	OMIM:256300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0002021	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000083	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003075	PMID:28392951	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0002020	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003073	PMID:28392951	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-02]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003270	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0002719	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0008677	PMID:17413422	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:256300	Nephrotic syndrome, type 1		HP:0012050	PMID:28392951	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:256300	Nephrotic syndrome, type 1		HP:0001967	OMIM:256300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003124	PMID:28392951	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-02]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000096	OMIM:256300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000093	PMID:28392951	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000092	OMIM:256300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000969	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0001518	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000007	PMID:9660941	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:256300	Nephrotic syndrome, type 1		HP:0000821	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0001510	OMIM:256300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0002643	OMIM:256300	IEA					P	HPO:iea[2009-02-17]
OMIM:256300	Nephrotic syndrome, type 1		HP:0003678	OMIM:256300	TAS					C	HPO:skoehler[2012-10-17]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0003577	PMID:18219278;PMID:19474805;PMID:16505000	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0025114	PMID:16505000	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0005595	PMID:16505000	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0025092	PMID:18219278;PMID:19474805;PMID:16505000	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0031288	PMID:16505000	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0040162	PMID:18219278	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0034703	PMID:16505000	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0008066	PMID:18219278;PMID:19474805;PMID:16505000	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0004906	PMID:18219278;PMID:19474805;PMID:16505000	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0001019	PMID:18219278;PMID:16505000	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0000007	PMID:16505000	PCS					I	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0007479	PMID:18219278;PMID:19474805;PMID:16505000	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620707	Epidermolytic hyperkeratosis 2B, autosomal recessive		HP:0000982	PMID:18219278;PMID:19474805;PMID:16505000	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0002421	PMID:30256902	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0000252	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0002521	PMID:30256902	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0001561	PMID:30256902	PCS	HP:0011461	1/2			P	HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0002650	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0002188	PMID:30256902	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0001250	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0001371	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0002120	PMID:30256902	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0000160	PMID:30256902	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0001285	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0001252	PMID:30256902	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0011344	PMID:23033978	PCS		1/1			P	HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0011097	PMID:30256902	PCS	HP:0003593	2/2			P	HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0032792	PMID:30256902	PCS	HP:0003593	2/2			P	HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0000729	PMID:30256902	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0000316	PMID:30256902	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0002119	PMID:30256902	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0200134	PMID:30256902	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0000369	PMID:30256902	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0000028	PMID:30256902	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0000006	PMID:30256902	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-25]
OMIM:618298	Developmental and epileptic encephalopathy 70		HP:0001249	PMID:30256902	PCS		2/2			P	HPO:probinson[2021-04-25]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000484	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0007759	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001498	OMIM:252600	TAS					P	HPO:probinson[2012-05-05]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001376	PMID:16094673	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0004322	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000243	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003593	PMID:30208878	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0034337	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000280	PMID:16094673;PMID:30208878	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09];ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0012666	PMID:15633164	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0011463	PMID:19659762;PMID:16094673	PCS		2/5			C	HPO:probinson[2022-05-08];HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0012471	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0011462	PMID:15633164	PCS		1/1			C	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001328	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003307	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001249	PMID:16094673	PCS		0/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000252	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003320	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001263	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0006380	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0012185	PMID:16094673	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000007	PMID:15633164	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001659	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000768	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000488	OMIM:252600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000763	PMID:15633164	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000520	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000369	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000885	OMIM:252600	TAS					P	HPO:probinson[2012-05-05]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001276	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003333	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000023	PMID:19197337;PMID:30208878	PCS		6/10			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09];ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0002240	PMID:19197337;PMID:30208878	PCS		6/13			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09];ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0002680	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001072	OMIM:252600	TAS					P	HPO:probinson[2012-05-05]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001508	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0008155	PMID:3777077;PMID:16094673;PMID:30208878	PCS		1/10			P	HPO:probinson[2024-03-09];HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09];ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000773	OMIM:252600	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0008439	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001744	PMID:30208878	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003026	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001363	PMID:30208878	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0004236	OMIM:252600	TAS					P	HPO:probinson[2012-05-05]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003621	PMID:19659762	PCS		3/4			C	HPO:probinson[2022-05-08]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003302	PMID:16094673	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0002650	PMID:16094673	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003264	PMID:15633164	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003182	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0005280	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0006162	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0002808	PMID:16094673	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001518	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000943	PMID:16094673	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0007178	PMID:15633164	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000546	PMID:20301730	TAS					P	HPO:skoehler[2010-06-20]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001638	PMID:15633164	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0003538	PMID:30208878	PCS		1/1			P	HPO:skoehler[2010-06-18]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0001357	PMID:30208878	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-27]
OMIM:252600	Mucolipidosis III alpha/beta		HP:0000303	OMIM:252600	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000286	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000164	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000486	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000023	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0001252	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0001290	OMIM:309610	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309610	Prieto syndrome		HP:0000939	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000639	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000316	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0009466	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0002999	PMID:3121220	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:309610	Prieto syndrome		HP:0000878	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0030084	PMID:3121220	PCS					P	HPO:skoehler[2014-09-21];HPO:probinson[2020-09-13]
OMIM:309610	Prieto syndrome		HP:0000278	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0001249	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0002059	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0001762	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0002673	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0010499	OMIM:309610	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309610	Prieto syndrome		HP:0001419	PMID:3121220	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:309610	Prieto syndrome		HP:0010781	PMID:3121220	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-13]
OMIM:309610	Prieto syndrome		HP:0000508	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000448	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000348	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000028	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:309610	Prieto syndrome		HP:0000369	OMIM:309610	IEA					P	HPO:iea[2009-02-17]
OMIM:161500	Nasal groove, familial transverse		HP:0000271	OMIM:161500	IEA					P	HPO:iea[2009-02-17]
OMIM:161500	Nasal groove, familial transverse		HP:0000006	OMIM:161500	IEA					I	HPO:iea[2009-02-17]
OMIM:615970	Alpha-Fetoprotein, hereditary persistence of		HP:0006254	PMID:14699509	PCS					P	HPO:probinson[2017-05-28]
OMIM:615970	Alpha-Fetoprotein, hereditary persistence of		HP:0000006	PMID:14699509	PCS					I	HPO:probinson[2017-05-28]
OMIM:165000	Ophthalmoplegia, familial static		HP:0009916	OMIM:165000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:165000	Ophthalmoplegia, familial static		HP:0000639	OMIM:165000	TAS					P	HPO:probinson[2009-02-17]
OMIM:165000	Ophthalmoplegia, familial static		HP:0000508	OMIM:165000	IEA					P	HPO:iea[2009-02-17]
OMIM:165000	Ophthalmoplegia, familial static		HP:0000602	OMIM:165000	IEA					P	HPO:iea[2009-02-17]
OMIM:165000	Ophthalmoplegia, familial static		HP:0000006	OMIM:165000	IEA					I	HPO:iea[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001276	PMID:18477710	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0010628	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0002540	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0003596	PMID:19955557	PCS		1/1			C	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001272	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001252	OMIM:128100	IEA					P	HPO:iea[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001290	OMIM:128100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001270	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0012048	PMID:19955557	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0000716	OMIM:128100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0003829	OMIM:128100	TAS					I	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0003307	OMIM:128100	IEA					P	HPO:iea[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0007325	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0002533	OMIM:128100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001304	OMIM:128100	TAS					P	HPO:probinson[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001347	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0003623	PMID:18477710	PCS		1/1			C	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0000473	OMIM:128100	IEA					P	HPO:iea[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0002015	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0002356	OMIM:128100	IEA					P	HPO:iea[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0002650	OMIM:128100	IEA					P	HPO:iea[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0003487	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001260	PMID:18477710	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0002808	OMIM:128100	IEA					P	HPO:iea[2009-02-17]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0002828	PMID:18477710	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0003438	PMID:19955557	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0000006	PMID:9288096	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0001337	PMID:19955557	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:128100	Dystonia 1, torsion, autosomal dominant		HP:0000643	OMIM:128100	IEA					P	HPO:iea[2009-02-17]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000286	PMID:36044892	PCS		9/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0010804	PMID:36044892	PCS		11/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000343	PMID:36044892	PCS		11/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0002188	PMID:36044892	PCS					P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0001252	PMID:36044892	PCS		3/23			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0001270	PMID:36044892	PCS		23/23			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000280	PMID:36044892	PCS		15/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0045075	PMID:36044892	PCS		8/44			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0012104	PMID:36044892	PCS		2/18			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0008070	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0033725	PMID:36044892	PCS		10/18			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000319	PMID:36044892	PCS		9/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000718	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0011220	PMID:36044892	PCS		12/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000739	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000316	PMID:36044892	PCS		3/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000954	PMID:36044892	PCS		3/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000219	PMID:36044892	PCS		5/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000752	PMID:36044892	PCS		6/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000179	PMID:36044892	PCS		1/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0001249	PMID:36044892	PCS		21/21			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000154	PMID:36044892	PCS		7/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0002212	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0002751	PMID:36044892	PCS		1/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000494	PMID:36044892	PCS		4/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0006956	PMID:36044892	PCS		3/18			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0001344	PMID:36044892	PCS		8/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000750	PMID:36044892	PCS		23/23			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0031936	PMID:36044892	PCS		21/21			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000276	PMID:36044892	PCS		4/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000232	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0005280	PMID:36044892	PCS		9/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0011447	PMID:36044892	PCS					P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0034295	PMID:36044892	PCS		1/18			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000407	PMID:36044892	PCS		1/23			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0032792	PMID:36044892	PCS		2/23			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000007	PMID:36044892	PCS					I	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0100716	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0004209	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0001335	PMID:36044892	PCS		1/23			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000664	PMID:36044892	PCS		7/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0001631	PMID:36044892	PCS		1/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0000369	PMID:36044892	PCS		1/22			P	HPO:probinson[2022-12-04]
OMIM:620075	Neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-Pelger-Huet anomaly		HP:0001655	PMID:36044892	PCS		2/22			P	HPO:probinson[2022-12-04]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0002465	PMID:19525954	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0000252	PMID:19525954	PCS		2/7			P	HPO:probinson[2012-04-11];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0000750	PMID:19525954	PCS		7/7			P	HPO:probinson[2012-04-11];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0001332	PMID:19525954	PCS		1/7			P	HPO:probinson[2012-04-11];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0001250	PMID:19525954	PCS		5/7			P	HPO:probinson[2012-04-11];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0002352	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0000295	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0001263	PMID:19525954	PCS		7/7			P	HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0001251	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0003593	PMID:19525954	PCS		7/7			C	HPO:probinson[2012-04-11];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0011400	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0011344	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0007042	OMIM:612951	TAS					P	HPO:skoehler[2013-01-22]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0000639	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0000407	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0000007	PMID:19525954	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0002119	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0002305	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0002514	OMIM:612951	IEA		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0001257	PMID:19525954	PCS		6/7			P	HPO:probinson[2012-04-11];HPO:probinson[2022-11-06]
OMIM:612951	Leukoencephalopathy, cystic, without megalencephaly		HP:0003677	OMIM:612951	TAS					C	HPO:skoehler[2013-01-22]
OMIM:261590	Phenformin 4-hydroxylation		HP:0000007	OMIM:261590	IEA					I	HPO:iea[2009-02-17]
OMIM:261590	Phenformin 4-hydroxylation		HP:0003128	OMIM:261590	IEA					P	HPO:iea[2009-02-17]
OMIM:612789	Deafness, autosomal recessive 71		HP:0000007	PMID:19229252	PCS					I	HPO:probinson[2017-06-25]
OMIM:612789	Deafness, autosomal recessive 71		HP:0000399	PMID:19229252	PCS					P	HPO:probinson[2017-06-25]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001254	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001344	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0002353	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0002540	OMIM:617829	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001288	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001332	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0011968	OMIM:617829	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001250	PMID:29100083	PCS		11/11			P	HPO:skoehler[2018-10-08];HP:probinson[2019-04-21]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001263	PMID:29100083	PCS		10/11			P	HPO:skoehler[2018-10-08];HP:probinson[2019-04-21]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001251	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0005484	PMID:29100083	PCS		6/11			P	HP:probinson[2019-04-21]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0100660	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0100704	OMIM:617829	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0003828	OMIM:617829	IEA					M	HPO:skoehler[2019-09-07]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0200134	PMID:29100083	PCS		11/11			P	HPO:skoehler[2018-10-08];HP:probinson[2019-04-21]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001257	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0000006	PMID:29100083	PCS					I	HPO:skoehler[2019-04-18];HP:probinson[2019-04-21]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001249	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617829	Epileptic encephalopathy, infantile or early childhood, 2		HP:0001336	OMIM:617829	IEA					P	HPO:skoehler[2018-10-08]
OMIM:160150	Centronuclear myopathy 1		HP:0001771	PMID:24465259	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003577	PMID:35081925;PMID:32826616	PCS		2/3			C	HPO:probinson[2022-05-14]
OMIM:160150	Centronuclear myopathy 1		HP:0003236	PMID:24465259	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0010628	PMID:22396310	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0005335	OMIM:160150	IEA					P	HPO:iea[2009-02-17]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0008948	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0001371	PMID:22396310	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:160150	Centronuclear myopathy 1		HP:0002460	PMID:24465259	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003593	PMID:35081925	PCS		1/2			C	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0001290	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0001270	OMIM:160150	IEA					P	HPO:iea[2009-02-17]
OMIM:160150	Centronuclear myopathy 1		HP:0030319	PMID:24465259	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0010546	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Centronuclear myopathy 1		HP:0011463	PMID:24465259	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Centronuclear myopathy 1		HP:0002938	PMID:24465259	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003307	PMID:22396310	PCS					P	HP:probinson[2019-03-01]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0007126	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003803	PMID:22396310	PCS					P	HP:probinson[2019-03-01]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003701	PMID:24465259	PCS		3/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-07-05]
OMIM:160150	Centronuclear myopathy 1		HP:0000597	PMID:24465259	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0030007	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003687	PMID:24465259;PMID:22396310;PMID:32826616	PCS		5/6			P	HPO:probinson[2022-05-14];HPO:skoehler[2010-06-20];HP:probinson[2019-03-01];HPO:probinson[2022-05-14];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Centronuclear myopathy 1		HP:0003621	PMID:24465259	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003388	OMIM:160150	IEA					P	HPO:iea[2009-02-17]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0001284	PMID:24465259;PMID:22396310	PCS		13/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0100284	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0008180	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0009053	PMID:32826616	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0000508	PMID:24465259;PMID:22396310	PCS		12/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Centronuclear myopathy 1		HP:0002505	PMID:24465259	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003712	PMID:32826616	PCS		0/1			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];HPO:probinson[2022-05-14]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0000006	PMID:22396310	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003677	OMIM:160150	IEA					C	HPO:iea[2009-02-17]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0003458	PMID:22396310	PCS					P	HP:probinson[2019-03-01]
OMIM:160150	Myopathy, centronuclear, autosomal dominant		HP:0000544	PMID:22396310	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:160150	Centronuclear myopathy 1		HP:0000467	PMID:24465259	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-05]
OMIM:619804	Deafness, autosomal dominant 82		HP:0003577	PMID:30535804	PCS		1/11			C	HPO:probinson[2022-05-14]
OMIM:619804	Deafness, autosomal dominant 82		HP:0003621	PMID:30535804	PCS		1/11			C	HPO:probinson[2022-05-14]
OMIM:619804	Deafness, autosomal dominant 82		HP:0003596	PMID:30535804	PCS		1/11			C	HPO:probinson[2022-05-14]
OMIM:619804	Deafness, autosomal dominant 82		HP:0011463	PMID:30535804	IEA		8/11			C	HPO:probinson[2022-05-14]
OMIM:619804	Deafness, autosomal dominant 82		HP:0000407	PMID:30535804	PCS		11/11			P	HPO:probinson[2022-05-14]
OMIM:619804	Deafness, autosomal dominant 82		HP:0000360	PMID:30535804	PCS		2/11			P	HPO:probinson[2022-05-14]
OMIM:619804	Deafness, autosomal dominant 82		HP:0000006	PMID:30535804	PCS					I	HPO:probinson[2022-05-14]
OMIM:245340	Erythrocyte lactate transporter defect		HP:0003236	PMID:10590411	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-07]
OMIM:245340	Erythrocyte lactate transporter defect		HP:0009020	PMID:10590411	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-07]
OMIM:245340	Erythrocyte lactate transporter defect		HP:0000006	PMID:10590411	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-07]
OMIM:245340	Erythrocyte lactate transporter defect		HP:0003710	PMID:10590411	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-07]
OMIM:245340	Erythrocyte lactate transporter defect		HP:0008967	PMID:10590411	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-07]
OMIM:245340	Erythrocyte lactate transporter defect		HP:0003457	PMID:10590411	PCS		0/5			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-11-07]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0000818	OMIM:129550	IEA					P	HPO:iea[2009-02-17]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0000684	OMIM:129550	IEA					P	HPO:iea[2009-02-17]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0002164	OMIM:129550	IEA					P	HPO:iea[2009-02-17]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0003187	OMIM:129550	IEA					P	HPO:iea[2009-02-17]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0000968	OMIM:129550	IEA					P	HPO:skoehler[2015-01-14]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0000966	OMIM:129550	IEA					P	HPO:iea[2009-02-17]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0002557	OMIM:129550	IEA					P	HPO:iea[2009-02-17]
OMIM:129550	Ectodermal dysplasia with adrenal cyst		HP:0000006	OMIM:129550	IEA					I	HPO:iea[2009-02-17]
OMIM:616289	Optic atrophy 9		HP:0003621	PMID:25351951	PCS		1/2			C	HPO:probinson[2022-10-11]
OMIM:616289	Optic atrophy 9		HP:0011463	PMID:25351951	PCS		1/2			C	HPO:probinson[2022-10-11]
OMIM:616289	Optic atrophy 9		HP:0007663	PMID:25351951	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-10-11]
OMIM:616289	Optic atrophy 9		HP:0000007	OMIM:616289	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616289	Optic atrophy 9		HP:0000505	PMID:25351951	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-11]
OMIM:616289	Optic atrophy 9		HP:0000648	PMID:25351951	PCS	HP:0011462	2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-11]
OMIM:616289	Optic atrophy 9		HP:0000642	PMID:25351951	PCS	HP:0011462	2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-11]
OMIM:616289	Optic atrophy 9		HP:0030528	PMID:25351951	PCS	HP:0011462	2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-10-11]
OMIM:616289	Optic atrophy 9		HP:0000543	PMID:25351951	PCS	HP:0011463	2/2			P	HPO:probinson[2022-10-11]
OMIM:615780	Retinitis pigmentosa 69		HP:0001133	PMID:24680887	PCS		2/3			P	HPO:probinson[2015-07-19];HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0000550	OMIM:615780	TAS	HP:0003596	1/3			P	HPO:probinson[2015-07-19];HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0034272	PMID:24680887	PCS		1/1			P	HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0003621	PMID:24680887	PCS		3/3			C	HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0000662	PMID:24680887	PCS		3/3			P	HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0000580	PMID:24680887	PCS		3/3			P	HPO:skoehler[2015-07-19];HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0000007	PMID:24680887	PCS					I	HPO:probinson[2015-07-19];HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0007663	PMID:24680887	PCS		2/3			P	HPO:probinson[2023-02-08]
OMIM:615780	Retinitis pigmentosa 69		HP:0000510	PMID:24680887	PCS		3/3			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-08]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0008066	OMIM:113800	TAS					P	HPO:probinson[2013-08-12]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0040189	OMIM:113800	TAS					P	HPO:skoehler[2015-10-05]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0007475	OMIM:113800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0025092	OMIM:113800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0001019	OMIM:113800	TAS					P	HPO:probinson[2009-02-17]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0000007	OMIM:113800	TAS					I	HPO:skoehler[2017-07-13]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0000972	OMIM:113800	TAS					P	HPO:skoehler[2013-05-03]
OMIM:113800	Epidermolytic hyperkeratosis		HP:0000006	OMIM:113800	IEA					I	HPO:iea[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0003577	PMID:27081549;PMID:8872475	PCS		8/8			C	HPO:probinson[2024-03-10];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0003016	PMID:27081549	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000541	PMID:15286167	PCS		17/31			P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-06]
OMIM:604841	Stickler syndrome, type II		HP:0000463	PMID:27081549;PMID:28971234	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2024-05-21];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:6000015	PMID:32901364	PCS		16/65			P	HPO:probinson[2024-01-06]
OMIM:604841	Stickler syndrome, type II		HP:0001252	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0003593	PMID:28971234	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0030839	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0012109	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000518	OMIM:604841	TAS					P	HPO:probinson[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0100807	OMIM:604841	TAS					P	HPO:probinson[2012-07-26]
OMIM:604841	Stickler syndrome, type II		HP:0003508	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0002757	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0007964	PMID:27081549	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0002655	OMIM:604841	TAS				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0001166	OMIM:604841	IEA					P	HPO:probinson[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0000175	PMID:15286167;PMID:27081549;PMID:28971234	PCS		8/33			P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-06];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0007968	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0030840	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0001382	PMID:15286167;PMID:28971234	PCS		9/32			P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-06];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000193	PMID:15286167;PMID:28971234	PCS		1/32			P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-06];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000272	OMIM:604841	TAS					P	HPO:probinson[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0003040	OMIM:604841	TAS					P	HPO:probinson[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0011800	PMID:15286167;PMID:28971234	PCS		19/32			P	HPO:skoehler[2015-11-15];HPO:probinson[2019-07-06];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0011003	PMID:8872475	PCS		7/7			P	HPO:probinson[2024-03-10]
OMIM:604841	Stickler syndrome, type II		HP:0005280	PMID:27081549;PMID:28971234	PCS		1/2			P	HPO:probinson[2012-07-26];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0034770	PMID:27081549	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000407	PMID:28971234;PMID:8872475	PCS		7/8			P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-06];HPO:probinson[2024-03-10];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0002705	PMID:15286167	PCS		3/31			P	HPO:probinson[2019-07-06]
OMIM:604841	Stickler syndrome, type II		HP:0007973	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000201	PMID:28971234	PCS		0/1			P	HPO:probinson[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0000586	PMID:27081549;PMID:28971234	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0004327	PMID:8872475	PCS		7/7			P	HPO:probinson[2012-07-26];HPO:probinson[2024-03-10]
OMIM:604841	Stickler syndrome, type II		HP:0000006	PMID:15286167	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2019-07-06]
OMIM:604841	Stickler syndrome, type II		HP:0000501	OMIM:604841	TAS					P	HPO:probinson[2009-02-17]
OMIM:604841	Stickler syndrome, type II		HP:0000347	PMID:28971234	PCS		0/1			P	HPO:probinson[2009-02-17];HPO:probinson[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000545	PMID:15286167	PCS	HP:0011463	27/31			P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-06]
OMIM:604841	Stickler syndrome, type II		HP:0000545	PMID:27081549	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:604841	Stickler syndrome, type II		HP:0000545	PMID:28971234	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:277480	von Willebrand disease, type 3		HP:0000132	OMIM:277480	TAS					P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0001892	OMIM:277480	TAS					P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0003125	PMID:2297569	PCS		1/1			P	HPO:probinson[2013-12-16];HPO:probinson[2023-02-18]
OMIM:277480	von Willebrand disease, type 3		HP:0003540	OMIM:277480	IEA					P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0003010	OMIM:277480	TAS					P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0005261	OMIM:277480	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0008330	PMID:2297569	PCS		1/1			P	HPO:probinson[2013-12-16];HPO:probinson[2023-02-18]
OMIM:277480	von Willebrand disease, type 3		HP:0000007	PMID:2297569	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-18]
OMIM:277480	von Willebrand disease, type 3		HP:0000978	OMIM:277480	TAS					P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0001934	OMIM:277480	TAS					P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0004846	OMIM:277480	IEA					P	HPO:skoehler[2018-10-08]
OMIM:277480	von Willebrand disease, type 3		HP:0000421	OMIM:277480	TAS					P	HPO:probinson[2009-02-17]
OMIM:277480	von Willebrand disease, type 3		HP:0001873	OMIM:277480	TAS					P	HPO:probinson[2009-02-17]
OMIM:617183	Harel-Yoon syndrome		HP:0003477	PMID:27640307	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000582	PMID:27640307	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0007957	PMID:27640307	PCS		1/8			P	HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0002540	PMID:27640307	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001332	PMID:27640307	PCS		1/8			P	HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001772	PMID:27640307	PCS		1/8			P	HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001272	PMID:27640307	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0003693	PMID:27640307	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0002121	PMID:27640307	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0003196	PMID:27640307	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001252	PMID:27640307	PCS		8/8			P	HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001251	PMID:27640307	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0003593	PMID:27640307	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0012708	PMID:27640307	PCS		2/3			P	HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000639	PMID:27640307	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000519	PMID:27640307	PCS	HP:0030674	2/8			P	HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001249	PMID:27640307	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0008936	PMID:27640307	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001385	PMID:27640307	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000750	PMID:27640307	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0002650	PMID:27640307	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000276	PMID:27640307	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0011968	PMID:27640307	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000490	PMID:27640307	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001263	PMID:27640307	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0002151	PMID:27640307	PCS		4/5			P	HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001639	PMID:27640307	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000007	PMID:27640307	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000348	PMID:27640307	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000648	PMID:27640307	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000768	PMID:27640307	PCS		2/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000565	PMID:27640307	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0002007	PMID:27640307	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0001257	PMID:27640307	PCS		5/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000006	PMID:27640307	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000303	PMID:27640307	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000347	PMID:27640307	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:617183	Harel-Yoon syndrome		HP:0000545	PMID:27640307	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-22]
OMIM:253250	Mulibrey nanism		HP:0000483	OMIM:253250	TAS					P	HPO:probinson[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0000486	PMID:7726235	PCS		6/42			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0004322	PMID:7726235	IEA		41/42			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0002783	PMID:7726235	PCS		13/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001052	PMID:7726235	PCS		21/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001252	PMID:7726235	PCS		31/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001131	PMID:7726235	PCS		4/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0002240	PMID:7726235	PCS		37/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0002680	PMID:7726235	PCS	HP:0011461	38/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0005132	PMID:7726235	PCS		31/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000580	PMID:7726235	PCS					P	HPO:probinson[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0003593	PMID:7726235	PCS		3/3			C	HPO:probinson[2022-03-25]
OMIM:253250	Mulibrey nanism		HP:0000935	PMID:7726235	PCS		8/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0006297	PMID:7726235	PCS		1/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000316	OMIM:253250	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000954	PMID:7726235	PCS		2/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000678	OMIM:253250	IEA					P	HPO:iea[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0002738	OMIM:253250	TAS					P	HPO:probinson[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0000612	PMID:7726235	PCS		1/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001789	PMID:7726235	PCS		1/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0002119	PMID:7726235	PCS		6/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001621	PMID:7726235	PCS		36/42			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001620	OMIM:253250	TAS					P	HPO:probinson[2013-04-12]
OMIM:253250	Mulibrey nanism		HP:0001685	OMIM:253250	IEA					P	HPO:iea[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0000431	OMIM:253250	TAS					P	HPO:probinson[2012-04-24]
OMIM:253250	Mulibrey nanism		HP:0001541	PMID:7726235	PCS		11/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001640	PMID:7726235	PCS		9/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001260	OMIM:253250	IEA					P	HPO:iea[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0000171	OMIM:253250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253250	Mulibrey nanism		HP:0005280	PMID:7726235	PCS		38/42			P	HPO:probinson[2012-04-24];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000668	OMIM:253250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253250	Mulibrey nanism		HP:0000007	PMID:10888877	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001635	OMIM:253250	IEA					P	HPO:iea[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0000689	PMID:7726235	PCS		19/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000268	OMIM:253250	IEA					P	HPO:iea[2009-02-17]
OMIM:253250	Mulibrey nanism		HP:0002007	PMID:7726235	PCS		36/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0002667	OMIM:253250;PMID:7726235	PCS		11/52			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001511	PMID:7726235	PCS	HP:0011461	14/38			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0001510	PMID:7726235	PCS		41/42			P	HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000325	PMID:7726235	PCS		41/42			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0002688	PMID:7726235	PCS		14/42			P	HPO:probinson[2012-06-10];HPO:probinson[2021-06-26]
OMIM:253250	Mulibrey nanism		HP:0000445	PMID:7726235	PCS		38/42			P	HPO:probinson[2021-06-26]
OMIM:619810	Deafness, autosomal dominant 84		HP:0003621	PMID:35278131	PCS					C	HPO:probinson[2022-04-16]
OMIM:619810	Deafness, autosomal dominant 84		HP:0003676	PMID:35278131	PCS					C	HPO:probinson[2022-04-16]
OMIM:619810	Deafness, autosomal dominant 84		HP:0000407	PMID:35278131	PCS					P	HPO:probinson[2022-04-16]
OMIM:619810	Deafness, autosomal dominant 84		HP:0011463	PMID:35278131	PCS					C	HPO:probinson[2022-04-16]
OMIM:619810	Deafness, autosomal dominant 84		HP:0011462	PMID:35278131	PCS					C	HPO:probinson[2022-04-16]
OMIM:619810	Deafness, autosomal dominant 84		HP:0000006	PMID:35278131	PCS					I	HPO:probinson[2022-04-16]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0004787	PMID:6306053	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002961	PMID:20926771	PCS		46/91			P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001399	PMID:6306053	PCS		1/6			P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0003496	OMIM:308240	IEA					P	HPO:iea[2009-02-17]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0011839	PMID:15761493	PCS		0/13			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002383	OMIM:308240	IEA					P	HPO:iea[2009-02-17]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002240	PMID:29649976;PMID:6306053	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-29];HPO:probinson[2022-08-07]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0003073	PMID:29649976	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002480	OMIM:308240	IEA					P	HPO:iea[2009-02-17]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0012177	PMID:29649976	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2022-08-07]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0012156	PMID:29649976;PMID:31754776;PMID:20926771;PMID:15761493	PCS		39/118			P	HPO:probinson[2022-08-07];HPO:probinson[2024-03-09];HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0011463	PMID:29649976	PCS		1/1			C	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0031693	PMID:20926771;PMID:15761493;PMID:6306053	PCS		16/110		HP:0033185	P	HPO:probinson[2024-03-09];HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002716	PMID:6306053	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0100827	OMIM:308240	IEA					P	HPO:skoehler[2018-10-08]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001744	PMID:6306053	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0004315	PMID:15761493	PCS		8/13			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002633	PMID:20926771	PCS		2/91			P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0030080	PMID:31754776	PCS		2/13		HP:0033185	P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001287	PMID:6306053	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0004313	PMID:31754776	PCS		10/13			P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0010975	PMID:31754776	PCS		0/7			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-09]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0011227	PMID:29649976	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0100776	OMIM:308240	TAS					P	HPO:probinson[2009-02-17]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001915	PMID:20926771	PCS		3/91			P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001419	PMID:9771704	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-22]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001954	PMID:29649976	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002205	PMID:6306053	PCS		2/6			P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001873	OMIM:308240	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002665	PMID:20926771;PMID:15761493	PCS		25/104			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-29];HPO:probinson[2024-03-09]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001876	PMID:29649976	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0001875	PMID:20926771	IEA		12/57			P	HPO:probinson[2020-10-29]
OMIM:308240	Lymphoproliferative syndrome, X-linked, 1		HP:0002721	PMID:31754776	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-29]
OMIM:620049	Nephrotic syndrome, type 26		HP:0003774	PMID:29534211	PCS		1/6			P	HPO:probinson[2022-10-02]
OMIM:620049	Nephrotic syndrome, type 26		HP:0000100	PMID:29534211	PCS	HP:0011463	6/6			P	HPO:probinson[2022-10-02]
OMIM:620049	Nephrotic syndrome, type 26		HP:0011463	PMID:29534211	PCS		6/6			C	HPO:probinson[2022-10-02]
OMIM:620049	Nephrotic syndrome, type 26		HP:0000097	PMID:29534211	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620049	Nephrotic syndrome, type 26		HP:0000007	PMID:29534211	PCS					I	HPO:probinson[2022-10-02]
OMIM:620049	Nephrotic syndrome, type 26		HP:0012588	PMID:29534211	PCS		2/6			P	HPO:probinson[2022-10-02]
OMIM:612776	Hypoglossia with situs inversus		HP:0003577	OMIM:612776	IEA					C	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0000750	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0001696	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0002098	OMIM:612776	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612776	Hypoglossia with situs inversus		HP:0000160	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0000171	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0002781	OMIM:612776	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612776	Hypoglossia with situs inversus		HP:0004395	OMIM:612776	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612776	Hypoglossia with situs inversus		HP:0000668	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0001746	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0008872	OMIM:612776	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612776	Hypoglossia with situs inversus		HP:0001748	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0000218	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0003745	OMIM:612776	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0000347	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612776	Hypoglossia with situs inversus		HP:0000369	OMIM:612776	IEA					P	HPO:skoehler[2010-06-19]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001133	PMID:15249642	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001250	PMID:10655068	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001392	PMID:10655068	PCS		0/2			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0000580	PMID:10655068	PCS		1/2			P	HPO:skoehler[2012-11-28];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001251	OMIM:614307	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:6000134	PMID:10655068	PCS		3/3			P	HPO:probinson[2024-01-13]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0033643	PMID:10655068	PCS		0/3			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0002080	PMID:15249642	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0007141	PMID:10655068	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0000815	OMIM:614307	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0000716	PMID:15249642	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0000518	PMID:15249642	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0011462	PMID:15249642	PCS		1/1			C	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0010571	PMID:10655068	PCS		3/3			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0000510	PMID:15249642	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001269	PMID:15249642	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001347	PMID:15249642	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0002133	OMIM:614307	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0002076	PMID:15249642	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001260	OMIM:614307	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0034449	PMID:31822849	PCS					P	HPO:probinson[2022-12-18]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0000007	PMID:10655068	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0000505	PMID:10655068	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001257	PMID:10655068	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0007359	PMID:15249642	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:614307	Alpha-methylacyl-CoA racemase deficiency		HP:0001337	PMID:15249642	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-12]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0005502	OMIM:266200	IEA					P	HPO:iea[2009-02-17]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0020181	PMID:35154711	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0003577	PMID:35168679	PCS		1/1			C	HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0020062	PMID:35168679;PMID:35154711	PCS		2/2			P	HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0000980	PMID:35154711	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0004870	OMIM:266200	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0001790	OMIM:266200	IEA		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0002240	PMID:35168679;PMID:35154711	PCS		2/2			P	HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0001081	OMIM:266200	IEA					P	HPO:iea[2009-02-17]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0001082	OMIM:266200	IEA					P	HPO:iea[2009-02-17]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0008282	OMIM:266200	TAS					P	HPO:probinson[2012-06-03]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0012132	PMID:35168679;PMID:35154711	PCS		2/2			P	HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0011463	PMID:35154711	IEA		1/1			C	HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0000007	PMID:1896471	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0001923	PMID:35154711	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0001511	OMIM:266200	IEA		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0001744	PMID:35168679;PMID:35154711	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02];HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0000952	PMID:35154711	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:266200	Pyruvate kinase deficiency of red cells		HP:0025109	PMID:35168679	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0002322	PMID:24700542	PCS		1/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001332	PMID:24700542	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001252	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0003593	PMID:24700542	PCS		1/2			C	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001270	PMID:24700542	PCS		1/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0100595	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0007166	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0000739	OMIM:606703	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0000317	PMID:24700542	PCS		1/2			P	HPO:probinson[2013-03-30];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0025336	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001347	PMID:24700542	PCS		1/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001644	OMIM:606703	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0008936	PMID:24700542	PCS		1/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0003621	PMID:24700542	PCS		1/2			C	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0003324	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0031936	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001266	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001260	PMID:24700542	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0002072	PMID:24700542	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0100660	PMID:24700542	PCS		1/2			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0002509	PMID:24700542	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001635	OMIM:606703	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0004305	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0000006	PMID:22782511	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0000467	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:606703	Dyskinesia, familial, with facial myokymia		HP:0001336	PMID:24700542	PCS		1/2			P	HPO:probinson[2022-08-18]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002069	PMID:25658047;PMID:26185144	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0000286	PMID:22368301	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0003236	PMID:25658047	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0000365	PMID:25658047;PMID:31396399;PMID:26185144;PMID:30659264	PCS		10/14			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001332	PMID:30659264	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002384	PMID:30659264	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0003198	PMID:31396399	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001250	PMID:25658047;PMID:30659264;PMID:31396399	PCS		10/13			P	ORCID:0000-0002-0736-9199[2024-10-08];HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0025664	PMID:25658047;PMID:26185144	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0012707	PMID:31396399	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001252	PMID:22368301	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-11-10]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001252	PMID:25658047	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001252	PMID:31396399	PCS		7/11			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001252	PMID:26185144	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001252	PMID:33704555	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001251	PMID:33704555;PMID:25658047	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0003593	PMID:25658047;PMID:31396399	PCS		8/16			C	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0032278	PMID:25658047;PMID:26185144	PCS		4/10			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0000280	PMID:22368301	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0011410	PMID:26185144	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0012666	PMID:25658047	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0033725	PMID:33704555;PMID:25658047;PMID:31396399	PCS		8/12			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0000639	PMID:30659264	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0011463	PMID:33704555	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0011461	PMID:25658047	PCS		3/5			C	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0007325	PMID:31396399	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001324	PMID:22368301	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001643	PMID:25658047	PCS		0/2			P	HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0003623	PMID:31396399;PMID:30659264	PCS		5/13			C	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0006813	PMID:33704555;PMID:25658047;PMID:26185144	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001662	PMID:25658047	PCS		1/3			P	HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001063	PMID:25658047	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0011924	PMID:33704555;PMID:30659264;PMID:26185144	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0011968	PMID:33704555;PMID:31396399;PMID:30659264;PMID:26185144	PCS		10/15			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001263	PMID:25658047;PMID:30659264;PMID:31396399	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002151	PMID:25658047;PMID:31396399;PMID:26185144;PMID:30659264	PCS		20/24			P	ORCID:0000-0002-0736-9199[2024-10-08];HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0000007	PMID:22368301	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-10]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0025722	PMID:31396399	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002505	PMID:31396399	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001257	PMID:33704555;PMID:25658047;PMID:31396399	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002104	PMID:25658047	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0003577	PMID:25658047;PMID:22368301;PMID:31396399;PMID:26185144	PCS		9/23			C	HPO:probinson[2022-11-10];ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001310	PMID:33704555	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001272	PMID:33704555;PMID:25658047;PMID:31396399	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001271	PMID:31396399	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0004383	OMIM:616276	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001270	PMID:33704555;PMID:25658047	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001508	PMID:30659264	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001629	PMID:22368301	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0100704	PMID:31396399	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001987	PMID:30659264	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0008314	PMID:33704555;PMID:30659264;PMID:26185144	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002910	PMID:25658047	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002059	PMID:31396399	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002015	PMID:25658047;PMID:26185144	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-10-08];HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0003621	PMID:33704555	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002650	PMID:25658047	PCS		1/1			P	HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001321	PMID:33704555;PMID:25658047;PMID:31396399;PMID:26185144	PCS		11/18			P	ORCID:0000-0002-0736-9199[2024-10-08];HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0005684	PMID:25658047	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001284	PMID:33704555;PMID:25658047	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0010851	PMID:33704555	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002172	PMID:25658047	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0034369	PMID:25658047;PMID:26185144	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002093	PMID:25658047	PCS	HP:0003623	3/3			P	HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002093	PMID:30659264	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0002093	PMID:26185144	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001639	PMID:25658047;PMID:30659264;PMID:31396399	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-10-08];HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0200134	PMID:25658047	PCS		1/3			P	HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0001511	PMID:25658047;PMID:26185144	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-10-08];HPO:skoehler[2015-04-19];HPO:probinson[2024-10-08]
OMIM:616276	Coenzyme Q10 deficiency, primary, 7		HP:0003259	PMID:25658047;PMID:30659264	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-10-08]
OMIM:619145	Spermatogenic failure 50		HP:0003251	PMID:30042186	PCS	HP:0003581	2/2			P	HPO:probinson[2021-01-01]
OMIM:619145	Spermatogenic failure 50		HP:0003251	PMID:30489636	PCS		1/1			P	HPO:probinson[2021-01-01]
OMIM:619145	Spermatogenic failure 50		HP:0000007	PMID:30042186	PCS					I	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619145	Spermatogenic failure 50		HP:0008734	PMID:30042186	PCS	HP:0003621	2/2			P	HPO:probinson[2021-01-01]
OMIM:619145	Spermatogenic failure 50		HP:0031038	PMID:30042186	PCS		2/2			P	HPO:probinson[2021-01-01]
OMIM:619145	Spermatogenic failure 50		HP:0000027	PMID:30042186;PMID:30489636	PCS		3/3			P	HPO:probinson[2021-01-01]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0003596	PMID:26838787	PCS		4/10			C	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0005113	PMID:26838787	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0012727	PMID:26838787	PCS		2/10			P	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0005112	OMIM:617168	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0031643	PMID:26838787	PCS		1/10			P	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0011462	PMID:26838787	PCS		4/10			C	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0002616	PMID:26838787	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0001647	PMID:26838787	PCS		3/10			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0000678	OMIM:617168	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0000218	PMID:26838787	PCS		1/10			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0004933	PMID:26838787	PCS		2/10			P	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0003621	PMID:26838787	PCS		2/10			C	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0002650	PMID:26838787	PCS		1/10			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0004970	PMID:26838787	PCS		3/10			P	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0001382	PMID:26838787	PCS		3/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0003584	PMID:26838787	PCS		2/10			C	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0001065	PMID:26838787	PCS		1/10			P	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0100775	PMID:26838787	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0001519	PMID:26838787	PCS		1/10			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0000767	PMID:26838787	PCS		1/10			P	HPO:skoehler[2019-04-18]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0001712	PMID:26838787	PCS		1/10			P	HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0001653	PMID:26838787	PCS		1/10			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0000006	PMID:26838787	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0000545	OMIM:617168	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617168	Aortic aneurysm, familial thoracic 10		HP:0001677	PMID:26838787	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0004322	PMID:11567216	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2020-07-15]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0010538	PMID:11567216	PCS		4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-07-15]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0000839	OMIM:262700	IEA					P	HPO:iea[2009-02-17]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0000821	OMIM:262700	IEA					P	HPO:iea[2009-02-17]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0001943	OMIM:262700	IEA					P	HPO:iea[2009-02-17]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0008850	OMIM:262700	IEA					P	HPO:iea[2009-02-17]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0031079	PMID:17065149	PCS					P	HPO:probinson[2020-07-15]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0000846	OMIM:262700	IEA					P	HPO:iea[2009-02-17]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0000006	PMID:11567216	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2020-07-15]
OMIM:262700	Pituitary hormone deficiency, combined, 4		HP:0003799	OMIM:262700	IEA					P	HPO:iea[2009-02-17]
OMIM:614475	Atrial septal defect 9		HP:0003577	PMID:20631719	PCS		2/2			C	HPO:probinson[2022-10-01]
OMIM:614475	Atrial septal defect 9		HP:0001684	PMID:20631719	PCS		2/4			P	HPO:skoehler[2013-06-11];HPO:probinson[2022-10-01]
OMIM:614475	Atrial septal defect 9		HP:0001647	PMID:20631719	PCS		1/4			P	HPO:probinson[2022-10-01]
OMIM:614475	Atrial septal defect 9		HP:0002092	PMID:20631719	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-01]
OMIM:614475	Atrial septal defect 9		HP:0000006	PMID:20631719	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-01]
OMIM:103420	Alacrima, congenital		HP:0000584	OMIM:103420	IEA					P	HPO:iea[2009-02-17]
OMIM:103420	Alacrima, congenital		HP:0000613	OMIM:103420	IEA					P	HPO:iea[2009-02-17]
OMIM:103420	Alacrima, congenital		HP:0007732	OMIM:103420	IEA					P	HPO:iea[2009-02-17]
OMIM:103420	Alacrima, congenital		HP:0007820	OMIM:103420	IEA					P	HPO:iea[2009-02-17]
OMIM:103420	Alacrima, congenital		HP:0000006	OMIM:103420	IEA					I	HPO:iea[2009-02-17]
OMIM:103420	Alacrima, congenital		HP:0000633	OMIM:103420	PCS					P	HPO:probinson[2012-04-01]
OMIM:103420	Alacrima, congenital		HP:0000522	OMIM:103420	PCS					P	HPO:probinson[2012-04-01]
OMIM:612004	Thrombocytopenia 4		HP:0011876	PMID:18345000	PCS		0/29			P	HPO:probinson[2022-07-20]
OMIM:612004	Thrombocytopenia 4		HP:0001873	OMIM:612004	TAS		29/29			P	HPO:probinson[2013-04-03];HPO:probinson[2022-07-20]
OMIM:612004	Thrombocytopenia 4		HP:0000006	PMID:18345000	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-07-20]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0003577	PMID:20037588	PCS		25/41			C	HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0010307	OMIM:606071	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0004322	OMIM:606071	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0008948	PMID:20037588	PCS		16/42			P	HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0000020	OMIM:606071	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0012246	OMIM:606071	TAS					P	HPO:probinson[2013-04-02]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0011463	PMID:20037588	PCS		10/41			C	HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0011462	PMID:20037588	PCS		6/41			C	HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0003829	OMIM:606071	TAS					I	HPO:skoehler[2012-10-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0009027	OMIM:606071	IEA					P	HPO:iea[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0002936	PMID:20037588	PCS		7/42			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0002878	OMIM:606071	TAS					P	HPO:probinson[2014-05-29]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0001604	PMID:20037588	PCS		11/42			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0007149	PMID:20037588	PCS		14/42			P	HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0003724	OMIM:606071	IEA					P	HPO:iea[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0004878	OMIM:606071	IEA					P	HPO:iea[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0200021	OMIM:606071	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0006897	OMIM:606071	TAS					P	HPO:probinson[2013-03-12]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0001765	OMIM:606071	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0001265	OMIM:606071	IEA					P	HPO:iea[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0002650	OMIM:606071	TAS		26/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0002870	OMIM:606071	IEA					P	HPO:iea[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0000012	OMIM:606071	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0001761	OMIM:606071	IEA					P	HPO:iea[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0008959	PMID:20037588	PCS		14/42			P	HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0001284	PMID:20037588	PCS		40/42			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0009130	OMIM:606071	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0009053	PMID:20037588	PCS		39/42			P	HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0000407	OMIM:606071	TAS					P	HPO:skoehler[2012-11-21]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0007230	OMIM:606071	IEA					P	HPO:iea[2009-02-17]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0009113	OMIM:606071	TAS					P	HPO:probinson[2014-05-29]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0000763	OMIM:606071	IEA					P	HPO:skoehler[2015-12-30]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0000006	PMID:20037588P	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606071	Hereditary motor and sensory neuropathy, type IIC		HP:0008944	PMID:20037588	PCS		39/42			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:151400	Leukemia, chronic lymphocytic		HP:0001442	OMIM:151400	TAS		20/20			I	HPO:iea[2009-02-17];HPO:skoehler[2012-10-17]
OMIM:151400	Leukemia, chronic lymphocytic		HP:0005550	OMIM:151400	IEA					P	HPO:iea[2009-02-17]
OMIM:151400	Leukemia, chronic lymphocytic		HP:0005374	OMIM:151400	IEA					P	HPO:iea[2015-05-23]
OMIM:126850	Duodenal ulcer, hyperpepsinogenemic I		HP:0000006	OMIM:126850	IEA					I	HPO:iea[2009-02-17]
OMIM:126850	Duodenal ulcer, hyperpepsinogenemic I		HP:0002588	OMIM:126850	IEA					P	HPO:iea[2009-02-17]
OMIM:126850	Duodenal ulcer, hyperpepsinogenemic I		HP:0003238	OMIM:126850	IEA					P	HPO:iea[2009-02-17]
OMIM:619151	AMED syndrome, digenic		HP:0000252	PMID:33355142	PCS		6/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0000013	PMID:33355142	PCS		1/6	FEMALE		P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0004322	PMID:33355142	PCS		7/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0005301	PMID:33355142	PCS		1/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0001882	PMID:33355142	PCS		4/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0010984	PMID:33355142	PCS					I	HPO:probinson[2021-03-05];HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0032524	PMID:33355142	PCS		1/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0001508	PMID:33355142	PCS		3/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0033044	PMID:33355142	PCS		4/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0000506	PMID:33355142	PCS		3/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0001903	PMID:33355142	PCS		6/6			P	HPO:probinson[2021-03-05];HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0004808	PMID:33355142	PCS		1/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0000729	PMID:33355142	PCS		1/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0000953	PMID:33355142	PCS		4/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0000835	PMID:33355142	PCS		1/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0000268	PMID:33355142	PCS		1/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0005528	PMID:33355142	PCS					P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0007018	PMID:33355142	PCS		1/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0001873	PMID:33355142	PCS		6/6			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0002863	PMID:33355142	PCS		6/7			P	HPO:probinson[2021-03-05]
OMIM:619151	AMED syndrome, digenic		HP:0001249	PMID:33355142	PCS		6/6			P	HPO:probinson[2021-03-05]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000164	PMID:29276006	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0003577	PMID:29276006	PCS		3/3			C	HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000343	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0001212	PMID:29276006	PCS		2/3			P	HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000463	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0001156	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0004322	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0003196	PMID:29276006	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000185	PMID:29276006	PCS		1/3			P	HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0004482	PMID:29276006	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0010292	PMID:29276006	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0010055	PMID:29276006	PCS		3/3			P	HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0001647	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000316	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0002933	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0030084	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000455	PMID:29276006	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000212	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000358	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0003027	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000750	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000431	PMID:29276006	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0001263	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0011800	PMID:29276006	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0011304	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0012385	PMID:29276006	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000007	PMID:29276006	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000348	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000527	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0001539	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000207	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0002007	PMID:29276006	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0001852	PMID:29276006	PCS		1/3			P	HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000520	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000369	PMID:29276006	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:618529	Robinow syndrome, autosomal recessive 2		HP:0000347	PMID:29276006	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-26]
OMIM:619637	Dystonia 32		HP:0000473	PMID:33452836	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0002015	PMID:33452836	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0002395	PMID:33452836	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0002451	PMID:33452836	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0001260	PMID:33452836	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0011462	PMID:33452836	PCS		1/1			C	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0000007	PMID:33452836	PCS					I	HPO:probinson[2022-01-24];HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0012444	PMID:33452836	PCS		1/1		HP:0012825	P	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0012049	PMID:33452836	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:619637	Dystonia 32		HP:0012753	PMID:33452836	PCS		1/1			P	HPO:probinson[2022-01-24]
OMIM:118000	Cervical vertebral bridge		HP:0000925	OMIM:118000	IEA					P	HPO:iea[2009-02-17]
OMIM:118000	Cervical vertebral bridge		HP:0000006	OMIM:118000	IEA					I	HPO:iea[2009-02-17]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0001892	OMIM:155100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0000077	PMID:10973259	PCS		0/10			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0000132	OMIM:155100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0003577	PMID:16969870	IEA		1/1			C	HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0003010	OMIM:155100	IEA					P	HPO:iea[2009-02-17]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0040185	PMID:15613099;PMID:16969870	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0031689	PMID:16969870	PCS		1/1			P	HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0040235	PMID:10973259	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0008264	PMID:10973259	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0000407	PMID:10973259;PMID:16969870	PCS		1/11			P	HPO:probinson[2022-04-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0001977	OMIM:155100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0001658	OMIM:155100	IEA					P	HPO:iea[2009-02-17]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0000978	OMIM:155100	TAS					P	HPO:probinson[2009-02-17]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0001902	PMID:10973259	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0008148	PMID:16969870	PCS		1/1			P	HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0000421	OMIM:155100	TAS					P	HPO:probinson[2009-02-17]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0001873	PMID:10973259	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0000006	PMID:10973259	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:155100	Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss		HP:0004866	PMID:16969870	PCS		1/1			P	HPO:probinson[2022-04-19]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0004322	OMIM:239710	TAS					P	HPO:probinson[2012-05-01]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000260	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0010055	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000316	OMIM:239710	TAS					P	HPO:probinson[2012-05-01]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000337	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000218	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0005989	OMIM:239710	TAS					P	HPO:skoehler[2015-01-20]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000358	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000396	OMIM:239710	PCS					P	HPO:iea[2011-12-18]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000494	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000252	OMIM:239710	TAS					P	HPO:probinson[2012-05-01]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000474	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0001161	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0011304	OMIM:239710	TAS					P	HPO:probinson[2012-05-01]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000508	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000349	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000007	OMIM:239710	IEA					I	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000048	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0001159	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000047	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000520	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000960	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000369	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000248	OMIM:239710	TAS					P	HPO:probinson[2012-05-01]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000049	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:239710	Acrofrontofacionasal dysostosis 2		HP:0000445	OMIM:239710	IEA					P	HPO:iea[2009-02-17]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0008936	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0008936	PMID:23339110	PCS	HP:0011463	3/3			P	HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0002540	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0000486	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0001344	PMID:23339110	PCS		3/3			P	HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0000496	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0001310	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0001250	PMID:23339110	PCS	HP:0003593	3/3			P	HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0001260	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0002066	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0001251	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0003593	OMIM:618501	IEA					C	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0002072	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0001290	PMID:23339110	PCS	HP:0003623	3/3			P	HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0012736	PMID:23339110	PCS		3/3			P	HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0000639	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0000817	OMIM:618501;PMID:23339110	PCS		13/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0001999	PMID:23339110	PCS		0/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0000007	PMID:23339110	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-27]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0200134	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0006855	OMIM:618501	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618501	Cerebellar atrophy with seizures and variable developmental delay		HP:0003623	PMID:23339110	PCS		3/3			C	HPO:probinson[2022-11-27]
OMIM:300813	Sarcoma, synovial		HP:0001442	OMIM:300813	IEA					I	HPO:probinson[2014-01-08]
OMIM:300813	Sarcoma, synovial		HP:0012570	OMIM:300813	IEA					P	HPO:probinson[2014-01-08]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0003202	PMID:23141294	PCS		8/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0001265	PMID:23141294	PCS		8/8			P	HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0003621	PMID:23141294	PCS		2/8			C	HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0001288	PMID:23141294	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0009053	PMID:23141294	PCS		8/8			P	HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0001761	PMID:23141294	PCS		8/8			P	HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0003474	PMID:23141294	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0011462	PMID:23141294	PCS		6/8			C	HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0006886	PMID:23141294	PCS		7/8			P	HPO:probinson[2022-03-20]
OMIM:615025	Charcot-Marie-Tooth disease, axonal, type 2Q		HP:0000006	PMID:23141294	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-20]
OMIM:613454	Rett syndrome, congenital variant		HP:0030215	PMID:21441262	PCS		6/10			P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0002188	PMID:28851325	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0001332	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0002186	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0001250	PMID:21441262	PCS		8/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0001252	PMID:28851325	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0002020	PMID:21441262	PCS		9/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0003593	PMID:28851325	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0001290	PMID:21441262	PCS		10/10			P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0025336	PMID:21441262;PMID:28851325	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0003745	OMIM:613454	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613454	Rett syndrome, congenital variant		HP:0002019	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0001763	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0003623	PMID:28851325	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0003763	PMID:21441262;PMID:28851325	PCS		8/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0000253	PMID:21441262	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0001344	PMID:21441262	PCS		11/11			P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0002353	PMID:28851325	PCS		3/4			P	HPO:skoehler[2014-05-04];HPO:probinson[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0002079	PMID:21441262;PMID:28851325	PCS		13/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0011968	PMID:21441262;PMID:28851325	PCS		12/15			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0001263	PMID:21441262;PMID:28851325	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0002072	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0011800	PMID:21441262	PCS					P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0100660	PMID:21441262	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0002307	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0002305	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0007359	PMID:28851325	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0001257	PMID:21441262	PCS		7/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0000006	PMID:21441262	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0001270	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0100703	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0000737	PMID:21441262	PCS		5/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0000817	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0000414	PMID:21441262	PCS					P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0000733	PMID:21441262;PMID:28851325	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0000219	PMID:21441262	PCS					P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0002835	PMID:21441262	PCS		6/10			P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0001302	PMID:21441262	PCS		3/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0000411	PMID:21441262	PCS					P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0000750	PMID:28851325	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0002650	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0001762	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0031936	PMID:21441262;PMID:28851325	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0002376	PMID:21441262;PMID:28851325	PCS		11/14			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2018-10-08];HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0005280	PMID:21441262	PCS					P	HPO:probinson[2021-02-07]
OMIM:613454	Rett syndrome, congenital variant		HP:0012760	PMID:21441262	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0002808	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0007333	PMID:28851325	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:613454	Rett syndrome, congenital variant		HP:0001319	OMIM:613454	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613454	Rett syndrome, congenital variant		HP:0009879	PMID:21441262	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-07]
OMIM:238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001250	OMIM:238340	IEA					P	HPO:iea[2009-02-17]
OMIM:238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001508	OMIM:238340	IEA					P	HPO:iea[2009-02-17]
OMIM:238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0000407	OMIM:238340	IEA					P	HPO:iea[2009-02-17]
OMIM:238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001939	OMIM:238340	IEA					P	HPO:iea[2009-02-17]
OMIM:238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0000007	OMIM:238340	IEA					I	HPO:iea[2009-02-17]
OMIM:238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0000546	OMIM:238340	IEA					P	HPO:iea[2009-02-17]
OMIM:238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001249	OMIM:238340	IEA					P	HPO:iea[2009-02-17]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0000286	PMID:21931173	PCS		8/13			P	HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0002023	PMID:2596524	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0008509	PMID:21931173	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0000294	PMID:21931173	PCS		16/19			P	HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0011336	PMID:21931173	PCS	HP:0003577	23/23			P	HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0011823	PMID:21931173	PCS		5/12			P	HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0005280	PMID:21931173	PCS		18/21			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0008070	PMID:21931173	PCS					P	HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0000629	PMID:21931173	PCS		23/23			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0000007	PMID:21931173	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0000414	PMID:21931173	PCS		17/19			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0009743	PMID:21931173	PCS		19/21			P	HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0000215	PMID:21931173	PCS		21/23			P	HPO:probinson[2020-02-15]
OMIM:227260	Focal facial dermal dysplasia 3, Setleis type		HP:0007646	PMID:2596524	PCS					P	HPO:probinson[2020-02-15]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000341	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000582	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0006989	PMID:32910914	PCS		2/6			P	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000343	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000243	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0004322	PMID:32910914	PCS		6/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0001250	PMID:33033404;PMID:32910914	PCS		7/13			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0030674	PMID:32910914	PCS		4/6			C	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0010808	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0003196	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0003593	PMID:32910914	PCS		2/6			C	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0001508	PMID:33033404	PCS		2/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0100704	PMID:32910914	PCS		3/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0012450	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000316	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0002119	PMID:33033404	PCS		1/3			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000637	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0006532	PMID:32910914	PCS		3/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0012171	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0001302	PMID:32910914	PCS		1/6			P	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000212	PMID:32910914	PCS		2/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0008936	PMID:32910914	PCS		2/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000252	PMID:33033404;PMID:32910914	PCS		13/13			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0002650	PMID:32910914	PCS		4/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0001344	PMID:32910914	PCS		2/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000750	PMID:33033404	PCS		5/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000431	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0002079	PMID:32910914	PCS		1/6			P	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0031936	PMID:33033404	PCS		3/3			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0011968	PMID:32910914	PCS		5/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0002373	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0001285	PMID:32910914	PCS		2/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0001263	PMID:33033404;PMID:32910914	PCS		13/13			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0012510	PMID:33033404	PCS		1/3			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0011231	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000426	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000307	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000006	PMID:32910914	PCS					I	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0009879	PMID:33033404;PMID:32910914	PCS		4/9			P	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0001655	PMID:32910914	PCS		1/7			P	HPO:probinson[2021-03-14]
OMIM:619179	Microcephaly 26, primary, autosomal dominant		HP:0000126	PMID:33033404	PCS		1/6			P	HPO:probinson[2021-03-14]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0003621	PMID:30068544	PCS		6/23			C	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0002860	PMID:30068544	PCS		14/21			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0002671	PMID:30068544	PCS		3/24			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0011463	PMID:30068544	PCS		16/23			C	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0011462	PMID:30068544	PCS		1/23			C	HPO:probinson[2023-02-19]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0025092	PMID:30068544	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0010610	OMIM:618267	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0000007	PMID:30068544	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618267	Epidermodysplasia verruciformis, susceptibility to, 3		HP:0200043	PMID:30068544	PCS		24/24			P	HPO:probinson[2023-02-19]
OMIM:275240	Tinea imbricata, susceptibility to		HP:0001939	OMIM:275240	IEA					P	HPO:iea[2009-02-17]
OMIM:275240	Tinea imbricata, susceptibility to		HP:0000007	OMIM:275240	IEA					I	HPO:iea[2009-02-17]
OMIM:275240	Tinea imbricata, susceptibility to		HP:0000951	OMIM:275240	IEA					P	HPO:iea[2009-02-17]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0001320	PMID:30449657	PCS		3/6			P	HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0002540	PMID:30449657	PCS		3/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0001344	PMID:30449657	PCS		5/6			P	HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0002078	PMID:30449657	PCS		1/6			P	HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0001321	PMID:30449657	PCS		5/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0002365	PMID:30449657	PCS		4/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0004322	PMID:30449657	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0001250	PMID:30449657	PCS		2/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0001263	PMID:30449657	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0003593	PMID:30449657	PCS		6/6			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0001290	PMID:30449657	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0007074	PMID:30449657	PCS		6/6			P	HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0007165	PMID:30449657	PCS		1/6			P	HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0000657	PMID:30449657	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0002317	PMID:30449657	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0002119	PMID:30449657	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0000006	PMID:30449657	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0001249	PMID:30449657	PCS		3/3			P	HPO:probinson[2023-01-15]
OMIM:618273	Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		HP:0009879	PMID:30449657	PCS		4/6			P	HPO:probinson[2023-01-15]
OMIM:617140	Zttk syndrome		HP:0000286	PMID:27545676;PMID:27256762	PCS		4/8			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000164	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0006989	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001773	PMID:27545680	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000486	PMID:27545680	PCS		11/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0004322	PMID:27545680	PCS		10/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000122	PMID:27545676	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001371	PMID:27545680	PCS		2/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001250	PMID:27545680	PCS		11/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000160	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0001252	PMID:27545676;PMID:27545680	PCS		20/26			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0003196	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000085	PMID:27545680	PCS		2/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0003593	PMID:25590979	PCS		1/1			C	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0004482	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0033128	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0045075	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0011100	PMID:25590979	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002937	PMID:27545680	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0011220	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0025336	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001643	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001249	PMID:27545680	PCS		20/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000176	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000891	PMID:27545676	PCS		2/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000494	PMID:27545676	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002079	PMID:27545676	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0011968	PMID:27545676	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000293	PMID:27545676;PMID:27256762	PCS		2/8			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001382	PMID:27545676	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000490	PMID:27545676	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001263	PMID:27545676;PMID:27256762;PMID:25590979	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0011800	PMID:27545676	PCS		6/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0030707	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000729	PMID:27545676	IEA		3/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000327	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000648	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0001659	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000322	PMID:27545676	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001257	PMID:27545676	PCS		1/6			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002500	PMID:27545680	PCS		4/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000006	PMID:27545680	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000369	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0000324	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0002028	PMID:27545676	PCS		2/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000341	PMID:27545676	PCS		2/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000540	PMID:27545680	PCS		6/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001508	PMID:27545676	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001629	PMID:27545676;PMID:25590979	PCS		2/8			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0100704	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0100702	PMID:27545676	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0008872	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0006970	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002119	PMID:27545680	PCS		14/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002714	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000218	OMIM:617140	TAS	HP:0003577				P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0000411	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000256	PMID:25590979	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001623	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000974	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002212	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0032989	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001363	PMID:27545680	PCS		3/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002650	PMID:27545676	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002133	PMID:27545680	PCS		1/20			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000233	PMID:27545676	PCS		5/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000431	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0001321	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0031936	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002376	PMID:27545676	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000193	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0011467	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0011229	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0005280	PMID:27256762	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002808	OMIM:617140	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617140	Zttk syndrome		HP:0000902	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001319	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0002007	PMID:27545676	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001511	PMID:27545676	PCS	HP:0011461	5/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0000103	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0200055	PMID:27545680	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001631	PMID:27545676	PCS		1/7			P	HPO:probinson[2021-05-01]
OMIM:617140	Zttk syndrome		HP:0001510	PMID:27256762	PCS		1/1			P	HPO:probinson[2021-05-01]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0002069	PMID:23176824	PCS		2/5			P	HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0001310	PMID:23176824	PCS					P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0004322	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0002066	PMID:23176824	PCS		4/4			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0001252	PMID:23176824	PCS		5/5			P	HPO:skoehler[2014-11-26]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0002020	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0002064	PMID:23176824	PCS		4/4			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0011463	PMID:23176824	PCS		5/5			C	HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000338	PMID:23176824	PCS		5/5			P	HPO:skoehler[2017-07-13]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000678	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000311	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0001249	PMID:23176824	PCS		5/5			P	HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0002059	PMID:23176824	PCS		2/2			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000252	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000475	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-08-11]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0002871	PMID:23176824	PCS		5/5		HP:0025303	P	HPO:skoehler[2013-06-06]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0002079	PMID:23176824	PCS		2/2			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0001260	PMID:23176824	PCS					P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0001263	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0001284	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000294	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000470	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-08-11]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000007	PMID:23176824	PCS					I	HPO:skoehler[2013-03-08];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0001258	PMID:23176824	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-05-20]
OMIM:615031	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay		HP:0000248	PMID:23176824	PCS		5/5			P	HPO:skoehler[2013-03-08]
OMIM:610149	Macular degeneration, age-related, 7		HP:0000608	OMIM:610149	TAS					P	HPO:probinson[2023-04-09]
OMIM:610149	Macular degeneration, age-related, 7		HP:0010982	OMIM:610149	TAS					I	HPO:probinson[2023-04-09]
OMIM:617626	Fibromatosis, gingival, 5		HP:0003621	PMID:28686854	PCS		2/8			C	HPO:probinson[2023-02-22]
OMIM:617626	Fibromatosis, gingival, 5		HP:0011463	PMID:28686854	PCS		6/8			C	HPO:probinson[2023-02-22]
OMIM:617626	Fibromatosis, gingival, 5		HP:0000766	PMID:28686854	PCS		3/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:617626	Fibromatosis, gingival, 5		HP:0000169	PMID:28686854	PCS		9/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:617626	Fibromatosis, gingival, 5		HP:0000006	PMID:28686854	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002421	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0003236	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0001252	OMIM:616538	TAS					P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0003593	PMID:24052401	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0001290	PMID:24052401	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0031882	OMIM:616538	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000518	PMID:24052401	PCS		1/2			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-03-01]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000557	PMID:24052401	PCS		1/2			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-03-01]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000238	OMIM:616538	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002878	OMIM:616538	TAS					P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002119	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002514	OMIM:616538	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002415	PMID:24052401	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000256	OMIM:616538	TAS					P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000556	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0001320	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0001344	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002079	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0001263	PMID:24052401	PCS		2/2		HP:0012828	P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002350	OMIM:616538	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0003560	OMIM:616538	TAS					P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0011003	PMID:24052401	PCS		1/2			P	HPO:probinson[2023-03-01];HPO:probinson[2023-03-01]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000007	PMID:24052401	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000568	OMIM:616538	TAS					P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0000501	OMIM:616538	TAS					P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0002126	PMID:24052401	PCS		2/2			P	HPO:skoehler[2015-10-05]
OMIM:616538	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9		HP:0003557	PMID:24052401	PCS		2/2			P	HPO:probinson[2023-03-01]
OMIM:243080	Inosine phosphorylase deficiency, immune defect due to		HP:0001939	OMIM:243080	IEA					P	HPO:iea[2009-02-17]
OMIM:243080	Inosine phosphorylase deficiency, immune defect due to		HP:0002715	OMIM:243080	IEA					P	HPO:iea[2009-02-17]
OMIM:243080	Inosine phosphorylase deficiency, immune defect due to		HP:0000007	OMIM:243080	IEA					I	HPO:iea[2009-02-17]
OMIM:300807	Thrombophilia, X-linked, due to factor IX defect		HP:0033061	PMID:19846852	PCS		1/1			P	HPO:probinson[2020-08-13]
OMIM:300807	Thrombophilia, X-linked, due to factor IX defect		HP:0001419	PMID:19846852	PCS					I	HPO:probinson[2020-07-24]
OMIM:300807	Thrombophilia, X-linked, due to factor IX defect		HP:0100724	PMID:19846852	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-08-13]
OMIM:300807	Thrombophilia, X-linked, due to factor IX defect		HP:0002625	PMID:19846852	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0005600	OMIM:137550	TAS					P	HPO:probinson[2012-08-01]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0003577	OMIM:137550	TAS					C	HPO:skoehler[2015-12-30]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000343	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0010759	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0002002	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000232	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000463	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0001442	PMID:23392294	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2020-07-20]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000293	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000194	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0025510	OMIM:137550	IEA					P	HPO:skoehler[2019-04-18]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0003196	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0012056	OMIM:137550	TAS					P	HPO:probinson[2012-08-01]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000418	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0011220	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000629	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000316	OMIM:137550	IEA					P	HPO:skoehler[2018-10-08]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000337	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000455	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:137550	Melanocytic nevus syndrome, congenital		HP:0000311	OMIM:137550	TAS					P	HPO:skoehler[2014-08-24]
OMIM:140900	Hemangiomas of small intestine		HP:0001048	OMIM:140900	TAS					P	HPO:iea[2009-02-17]
OMIM:140900	Hemangiomas of small intestine		HP:0000006	OMIM:140900	IEA					I	HPO:iea[2009-02-17]
OMIM:609197	Glucocorticoid deficiency 3		HP:0008163	PMID:12384787	PCS		10/10			P	HPO:probinson[2024-03-14]
OMIM:609197	Glucocorticoid deficiency 3		HP:0003154	PMID:12384787	PCS		8/8			P	HPO:probinson[2024-03-14];HPO:probinson[2024-03-14]
OMIM:609197	Glucocorticoid deficiency 3		HP:0001988	PMID:12384787	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609197	Glucocorticoid deficiency 3		HP:0040084	PMID:12384787	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-14]
OMIM:609197	Glucocorticoid deficiency 3		HP:0000007	PMID:12384787	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609197	Glucocorticoid deficiency 3		HP:0000953	PMID:12384787	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609197	Glucocorticoid deficiency 3		HP:0004319	PMID:12384787	PCS		2/3			P	HPO:probinson[2024-03-14]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0002850	PMID:23000145	PCS		2/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0006515	PMID:23000145	PCS		2/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0005425	PMID:23000145	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0004387	PMID:23000145	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0030388	PMID:23000145	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0003593	PMID:23000145	PCS		2/2			C	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0010783	PMID:23000145	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0011950	PMID:23000145	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0100279	PMID:23000145	PCS		1/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0002829	PMID:23000145	PCS		2/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0000518	PMID:23000145	PCS		1/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0100658	PMID:23000145	PCS		2/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0002958	PMID:23000145	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0000006	PMID:23000145	PCS					I	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0200020	PMID:23000145	PCS		1/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:614878	Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated		HP:0002720	PMID:23000145	PCS		2/2			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-08-27]
OMIM:300436	Intellectual developmental disorder, X-linked 46		HP:0000407	OMIM:300436	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:300436	Intellectual developmental disorder, X-linked 46		HP:0001419	OMIM:300436	TAS					I	HPO:probinson[2009-02-17]
OMIM:300436	Intellectual developmental disorder, X-linked 46		HP:0001249	OMIM:300436	TAS					P	HPO:probinson[2009-02-17]
OMIM:618924	Episodic ataxia, type 9		HP:0002069	PMID:26645390	PCS	HP:0003623	3/4			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0002069	PMID:27159988	PCS		1/1			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0001298	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0002133	PMID:27159988	PCS		1/1			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0002013	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0001332	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0002321	PMID:27159988	PCS		1/1			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0025335	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0001250	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0002131	PMID:27159988	PCS		1/1			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0010532	PMID:26645390	PCS		2/4			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0030915	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0000639	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0032792	PMID:26645390	PCS	HP:0003623	1/4			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0032792	PMID:27159988	PCS		1/1			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0100702	PMID:27328862	PCS		1/1			P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0020221	PMID:26645390	PCS	HP:0003623	1/4			P	HPO:probinson[2020-09-02]
OMIM:618924	Episodic ataxia, type 9		HP:0000006	PMID:26645390	PCS					I	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:620277	Spermatogenic failure 81		HP:0034011	PMID:36708031	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620277	Spermatogenic failure 81		HP:0003251	PMID:36708031	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620277	Spermatogenic failure 81		HP:0000007	PMID:36708031	PCS					I	HPO:probinson[2023-07-07]
OMIM:620277	Spermatogenic failure 81		HP:0006321	PMID:36708031	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620277	Spermatogenic failure 81		HP:0000798	PMID:36708031	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620277	Spermatogenic failure 81		HP:0034913	PMID:36708031	PCS		2/2			P	HPO:probinson[2023-07-18]
OMIM:300422	Fg syndrome 4		HP:0000431	PMID:19200522	PCS					P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0002650	PMID:19200522	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0001250	PMID:19200522	PCS		5/8			P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0000407	PMID:19200522	PCS		4/6			P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0001263	PMID:19200522	PCS					P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0011220	PMID:19200522	PCS		3/8			P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0000316	PMID:19200522	PCS					P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0008872	PMID:19200522	PCS		5/8			P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0001319	PMID:19200522	PCS		6/8			P	HPO:probinson[2013-02-17]
OMIM:300422	Fg syndrome 4		HP:0001417	PMID:19200522	PCS					I	HPO:probinson[2013-01-09]
OMIM:300422	Fg syndrome 4		HP:0001249	PMID:19200522	PCS					P	HPO:probinson[2013-02-17]
OMIM:613865	Deafness, autosomal recessive 61		HP:0000407	PMID:12719379	PCS	HP:0003577				P	HPO:probinson[2013-02-18]
OMIM:613865	Deafness, autosomal recessive 61		HP:0000007	PMID:12719379	PCS					I	HPO:probinson[2013-02-18]
OMIM:204650	Amelogenesis imperfecta, type IC		HP:0000705	PMID:14684688	PCS		3/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:204650	Amelogenesis imperfecta, type IC		HP:0006285	PMID:14684688	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:204650	Amelogenesis imperfecta, type IC		HP:0009102	PMID:14684688	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:204650	Amelogenesis imperfecta, type IC		HP:0006286	PMID:14684688	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:204650	Amelogenesis imperfecta, type IC		HP:0000679	PMID:14684688	PCS		0/3			P	HPO:probinson[2022-09-02]
OMIM:204650	Amelogenesis imperfecta, type IC		HP:0000007	PMID:14684688	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001276	PMID:32730804	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000286	PMID:32730804;PMID:36333968	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0003577	PMID:32730804	PCS		1/9			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0002144	PMID:37394306;PMID:32730804	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0002023	PMID:32730804	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000343	PMID:36333968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000122	PMID:32730804	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001250	PMID:37394306;PMID:32730804;PMID:36333968	PCS		7/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001272	PMID:37394306;PMID:32730804;PMID:36333968	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001252	PMID:32730804	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0003593	PMID:32730804;PMID:36333968	PCS		9/10			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0012304	PMID:32730804	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001629	PMID:32730804	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0011463	PMID:37394306	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000718	PMID:32730804;PMID:36333968	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001647	PMID:32730804	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001822	PMID:32730804;PMID:36333968	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0020045	PMID:36333968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000414	PMID:36333968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000218	PMID:36333968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001763	PMID:36333968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001249	PMID:37394306;PMID:36333968	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0002435	PMID:37394306;PMID:32730804;PMID:36333968	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0002575	PMID:32730804	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000252	PMID:32730804;PMID:36333968	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000750	PMID:32730804;PMID:36333968	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0002650	PMID:32730804;PMID:36333968	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0031936	PMID:32730804;PMID:36333968	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0002079	PMID:37394306;PMID:32730804;PMID:36333968	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0011968	PMID:36333968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001382	PMID:36333968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001263	PMID:37394306;PMID:32730804;PMID:36333968	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0002808	PMID:32730804;PMID:36333968	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000729	PMID:32730804;PMID:36333968	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000767	PMID:32730804;PMID:36333968	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0100716	PMID:32730804;PMID:36333968	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000003	PMID:32730804	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0001513	PMID:32730804;PMID:36333968	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000006	PMID:32730804	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620511	Fliedner-Zweier syndrome		HP:0000126	PMID:32730804	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614844	Nephronophthisis 14		HP:0001320	OMIM:614844	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614844	Nephronophthisis 14		HP:0001696	OMIM:614844	TAS		HP:0040283			P	HPO:skoehler[2012-12-02]
OMIM:614844	Nephronophthisis 14		HP:0000090	OMIM:614844	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614844	Nephronophthisis 14		HP:0000546	OMIM:614844	TAS		HP:0040283			P	HPO:skoehler[2012-12-02]
OMIM:614844	Nephronophthisis 14		HP:0000007	OMIM:614844	TAS					I	HPO:skoehler[2012-12-02]
OMIM:614844	Nephronophthisis 14		HP:0000113	OMIM:614844	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614844	Nephronophthisis 14		HP:0000006	OMIM:614844	TAS					I	HPO:skoehler[2012-12-02]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0010804	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001531	PMID:23824657	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0004322	PMID:25835445	PCS		1/43			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001052	PMID:23824657	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0003199	PMID:23824657	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001252	PMID:24798638;PMID:23824657	PCS		2/2			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000283	PMID:24798638	PCS		1/1			P	HPO:skoehler[2015-10-05];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0410151	PMID:23608731	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0010646	PMID:25835445	PCS		1/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000319	PMID:24798638	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000316	PMID:25835445;PMID:24798638;PMID:23824657	PCS		16/45			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0002616	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000637	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000278	PMID:23824657	PCS		1/1		HP:0012825	P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001763	PMID:25835445;PMID:23824657	PCS		15/44			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0002751	PMID:25835445;PMID:24798638	PCS		12/44			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0002036	PMID:25835445	PCS		3/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000098	PMID:25835445	PCS		12/43			P	HPO:skoehler[2015-07-26]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000494	PMID:24798638	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000175	PMID:25835445	PCS		5/43			P	HPO:skoehler[2015-07-26]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001382	PMID:25835445;PMID:24798638;PMID:23824657	PCS		11/45			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0011800	PMID:24798638	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0002194	PMID:23824657	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000767	PMID:25835445;PMID:24798638;PMID:23824657	PCS		13/45		HP:0012825	P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0003758	PMID:24798638;PMID:23824657	PCS		2/2			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000768	PMID:25835445	PCS					P	HPO:skoehler[2015-07-26]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000520	PMID:23824657	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001653	PMID:25835445	PCS		4/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000248	PMID:24798638	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000006	PMID:25835445	PCS					I	HPO:skoehler[2014-01-28]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001655	PMID:25835445	PCS		1/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0005830	PMID:23824657	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000023	PMID:25835445	PCS		4/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0003691	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000185	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0010665	PMID:25835445;PMID:23824657	PCS		2/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0011833	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0012771	PMID:25835445	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001629	PMID:25835445	PCS		1/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001548	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000978	PMID:25835445	PCS		4/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0002758	PMID:25835445	PCS		2/43			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000218	PMID:25835445	PCS		4/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0004933	PMID:25835445	PCS		3/43			P	HP:probinson[2018-07-07]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000396	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001166	PMID:25835445;PMID:24798638	PCS		17/44			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0003302	PMID:25835445	PCS		1/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001762	PMID:25835445	PCS		1/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000276	PMID:25835445	PCS		4/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000193	PMID:25835445;PMID:24798638;PMID:23824657	PCS		13/45			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000592	PMID:23824657	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000508	PMID:24798638	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000426	PMID:24798638	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001319	PMID:23824657	PCS		1/1			P	HP:probinson[2018-05-03];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0000268	PMID:25835445	PCS		3/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001510	PMID:23824657	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0005879	PMID:23824657	PCS		1/1			P	HPO:probinson[2021-05-23]
OMIM:615582	Loeys-Dietz syndrome 5		HP:0001631	PMID:25835445	PCS		1/43			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-05-23]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000365	PMID:24259288;PMID:34875027	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001399	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001250	PMID:24259288;PMID:34875027	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001272	PMID:24259288;PMID:34875027	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001371	PMID:24259288;PMID:34875027	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0003452	PMID:24259288;PMID:34875027	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0003155	PMID:34875027	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001051	PMID:24259288;PMID:34875027	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001252	PMID:24259288;PMID:34875027	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001394	PMID:24259288;PMID:34875027	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0002240	PMID:24259288;PMID:34875027	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001251	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0003593	PMID:24259288;PMID:34875027	PCS		6/6			C	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000280	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0100704	PMID:24259288;PMID:34875027	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001548	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0006895	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000212	PMID:24259288;PMID:34875027	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001744	PMID:24259288;PMID:34875027	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001347	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0003700	PMID:24259288;PMID:34875027	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0500200	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0008936	PMID:24259288	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0002059	PMID:24259288;PMID:34875027	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000252	PMID:24259288;PMID:34875027	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0002133	PMID:24259288;PMID:34875027	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0002650	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001344	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0003487	PMID:24259288;PMID:34875027	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0002376	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001263	PMID:24259288;PMID:34875027	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000691	PMID:24259288;PMID:34875027	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0002174	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001182	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0003281	PMID:24259288;PMID:34875027	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0031876	PMID:34875027	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0012463	PMID:24259288;PMID:34875027	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0008064	PMID:24259288;PMID:34875027	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0012465	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001419	PMID:24259288	PCS					I	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001357	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001257	PMID:24259288;PMID:34875027	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000047	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001873	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000028	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0000687	PMID:24259288;PMID:34875027	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:301072	Neurodevelopmental disorder with epilepsy and hemochromatosis		HP:0001336	PMID:24259288;PMID:34875027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0002510	PMID:24784932	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0010837	PMID:24784932	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0002079	PMID:24784932	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0001263	PMID:24784932	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0001252	PMID:24784932	PCS		0/1			P	HPO:probinson[2022-10-31];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0010818	PMID:24784932	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0003593	PMID:24784932	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0005484	PMID:24784932	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0012506	PMID:24784932	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0011967	PMID:24784932	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0012345	PMID:24784932	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0002506	PMID:24784932	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0000007	PMID:24784932	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:617395	Congenital disorder of glycosylation, type IIq		HP:0002910	PMID:24784932	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-31]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000286	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0010803	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0001212	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0002442	PMID:30150678	PCS		4/15			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0010522	PMID:30150678	PCS		6/15			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0002282	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0011182	PMID:29738522	PCS		3/5			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0011342	PMID:29738522	PCS		5/10			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0008551	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000954	PMID:31317654	PCS		1/1		HP:0012833	P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0030084	PMID:29738522	PCS		1/5			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000218	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000212	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000358	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0001007	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0001249	PMID:31317654;PMID:30150678	PCS		12/16			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0005326	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000252	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0002136	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000750	PMID:31317654;PMID:29738522	PCS		2/6			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0002079	PMID:31317654;PMID:29738522	PCS		4/6			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0001761	PMID:29738522	PCS		1/5			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0030026	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0005487	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0001263	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0032388	PMID:30150678;PMID:29738522	PCS		13/20			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0001182	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000729	PMID:30150678	PCS		4/15			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000722	PMID:30150678	PCS		2/15			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0004209	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000664	PMID:31317654	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0007359	PMID:29738522	PCS	HP:0011463	2/5			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0007018	PMID:31317654;PMID:30150678	PCS		6/16			P	HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0000006	PMID:29738522	PCS					I	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618918	Periventricular nodular heterotopia 9		HP:0002126	PMID:29738522	PCS		3/5			P	HPO:probinson[2020-08-11]
OMIM:205200	Amyotrophic lateral sclerosis, juvenile, with dementia		HP:0003693	OMIM:205200	IEA					P	HPO:iea[2009-02-17]
OMIM:205200	Amyotrophic lateral sclerosis, juvenile, with dementia		HP:0000726	OMIM:205200	IEA					P	HPO:iea[2009-02-17]
OMIM:205200	Amyotrophic lateral sclerosis, juvenile, with dementia		HP:0007354	OMIM:205200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:205200	Amyotrophic lateral sclerosis, juvenile, with dementia		HP:0000007	OMIM:205200	IEA					I	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0003651	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001332	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001250	PMID:11182931	PCS		12/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:257220	Niemann-pick disease, type C1		HP:0002066	PMID:12408188	PCS		4/4			P	HPO:probinson[2021-09-24]
OMIM:257220	Niemann-pick disease, type C1		HP:6000158	PMID:25665455	PCS					P	HPO:probinson[2024-01-13]
OMIM:257220	Niemann-pick disease, type C1		HP:0001791	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001252	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0002185	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001251	PMID:11182931	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:257220	Niemann-pick disease, type C1		HP:0002240	PMID:11182931	PCS		7/13			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:257220	Niemann-pick disease, type C1		HP:0001290	OMIM:257220	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257220	Niemann-pick disease, type C1		HP:0011462	PMID:12408188	PCS		1/4			C	HPO:probinson[2021-09-24]
OMIM:257220	Niemann-pick disease, type C1		HP:0003349	PMID:3378364;PMID:12408188	PCS		13/13			P	HPO:iea[2009-02-17];HP:probinson[2019-01-23];HPO:probinson[2021-09-24];HPO:probinson[2021-09-24]
OMIM:257220	Niemann-pick disease, type C1		HP:0006579	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001744	PMID:11182931	PCS		4/13			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:257220	Niemann-pick disease, type C1		HP:0001249	PMID:12408188	PCS	HP:0003621	4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-24]
OMIM:257220	Niemann-pick disease, type C1		HP:0000511	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0002015	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0003621	PMID:12408188	PCS		3/4			C	HPO:probinson[2021-09-24]
OMIM:257220	Niemann-pick disease, type C1		HP:0003640	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001982	PMID:12408188	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-24]
OMIM:257220	Niemann-pick disease, type C1		HP:0004333	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001260	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0002371	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001263	PMID:11182931	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:257220	Niemann-pick disease, type C1		HP:0000709	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0000726	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0006583	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0002529	OMIM:257220	IEA					P	HPO:skoehler[2010-06-20]
OMIM:257220	Niemann-pick disease, type C1		HP:0000007	PMID:11182931	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:257220	Niemann-pick disease, type C1		HP:0002524	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:257220	Niemann-pick disease, type C1		HP:0001257	OMIM:257220	IEA					P	HPO:iea[2009-02-17]
OMIM:248300	Meleda disease		HP:0033194	PMID:11285253	PCS					P	HPO:probinson[2021-03-13]
OMIM:248300	Meleda disease		HP:0001808	OMIM:248300	TAS					P	HPO:probinson[2009-02-17]
OMIM:248300	Meleda disease		HP:0001156	PMID:11285253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:248300	Meleda disease		HP:0008064	PMID:11285253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:248300	Meleda disease		HP:0003593	OMIM:248300	IEA					C	HPO:iea[2009-02-17]
OMIM:248300	Meleda disease		HP:0000007	PMID:14674887	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:248300	Meleda disease		HP:0000975	PMID:11285253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:248300	Meleda disease		HP:0007553	PMID:11285253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:613695	Long QT syndrome 5		HP:0001663	PMID:20823649	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:613695	Long QT syndrome 5		HP:0025708	PMID:20823649	PCS		2/2			C	HPO:probinson[2022-07-09]
OMIM:613695	Long QT syndrome 5		HP:0005184	PMID:9354802;PMID:20823649	PCS		6/7			P	HPO:probinson[2022-07-09]
OMIM:613695	Long QT syndrome 5		HP:0001279	OMIM:613695	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613695	Long QT syndrome 5		HP:0001664	OMIM:613695	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613695	Long QT syndrome 5		HP:0000006	PMID:9354802	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:613695	Long QT syndrome 5		HP:0001645	OMIM:613695	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613695	Long QT syndrome 5		HP:0001688	PMID:20823649	PCS		2/2			P	HPO:probinson[2022-07-09]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0001199	PMID:20577005	PCS		1/4			P	HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0011939	PMID:21654727	IEA		2/2			P	HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0003577	PMID:20577005;PMID:21654727	PCS		5/6			C	HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0001762	PMID:20577005	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0004322	PMID:20577005	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0011463	PMID:20577005	PCS		1/4			C	HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0012043	PMID:20577005	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0009777	PMID:20577005	PCS		1/4			P	HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0009778	PMID:20577005	PCS		1/4			P	HPO:probinson[2022-03-27]
OMIM:613681	Chromosome 2q31.1 duplication syndrome		HP:0000006	PMID:20577005	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0002487	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0008936	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0002310	OMIM:616921	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0001250	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0011968	OMIM:616921	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0001260	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0003593	OMIM:616921	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0002072	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0001270	OMIM:616921	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0100660	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0100248	OMIM:616921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0000007	PMID:27058446	PCS					I	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0002317	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0002307	PMID:27058446	PCS					P	HPO:probinson[2017-06-23]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0002359	OMIM:616921	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616921	Dyskinesia, limb and orofacial, infantile-onset		HP:0001337	OMIM:616921	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611096	Intellectual developmental disorder, autosomal recessive 10		HP:0001250	OMIM:611096	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611096	Intellectual developmental disorder, autosomal recessive 10		HP:0000007	OMIM:611096	TAS					I	HPO:skoehler[2017-07-13]
OMIM:611096	Intellectual developmental disorder, autosomal recessive 10		HP:0001270	OMIM:611096	TAS					P	HPO:skoehler[2017-07-13]
OMIM:301700	ANOSMIA		HP:0000458	OMIM:301700	IEA					P	HPO:iea[2009-02-17]
OMIM:301700	ANOSMIA		HP:0001417	OMIM:301700	IEA					I	HPO:iea[2009-02-17]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000286	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000486	PMID:31833172;PMID:30595499	PCS		3/7			P	HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001377	PMID:30595499	PCS		1/4			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001250	PMID:30595499	PCS		4/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001252	PMID:31833172	PCS		2/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001010	PMID:31833172;PMID:30595499	PCS		6/7		HP:0025293	P	HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0410030	PMID:30595499	PCS		1/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000280	PMID:31833172;PMID:30595499	PCS		6/7			P	HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0500041	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0012471	PMID:30595499	PCS		2/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000718	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000316	PMID:30595499	PCS		4/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0003307	PMID:30595499	PCS		2/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000956	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0002857	PMID:30595499	PCS		1/4			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001763	PMID:30595499	PCS		3/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000358	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001249	PMID:31833172	PCS		2/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001385	PMID:30595499	PCS		1/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000494	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000175	PMID:30595499	PCS		1/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001344	PMID:31833172	PCS		2/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000293	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0011803	PMID:30595499	PCS		1/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001263	PMID:31833172;PMID:30595499	PCS		12/12			P	HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001182	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0012016	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0012017	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0002827	PMID:30595499	PCS		1/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000729	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0031165	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001537	PMID:31833172;PMID:30595499	PCS		3/7			P	HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000646	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000403	PMID:31833172	PCS		2/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001417	PMID:30595499	PCS					I	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000885	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001230	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0002240	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0012014	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0006371	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0012450	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000733	PMID:31833172	PCS		2/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001943	PMID:30595499	PCS	HP:0003623	2/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000736	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000256	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001762	PMID:30595499	PCS		1/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000750	PMID:30595499	PCS					P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000232	PMID:31833172	PCS		2/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0002376	PMID:30595499	PCS		1/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000194	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000272	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001081	PMID:31833172	PCS		2/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001082	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0005280	PMID:30595499	PCS		3/5			P	HPO:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000826	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000508	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000664	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001433	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0001513	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:301066	Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies		HP:0000545	PMID:31833172	PCS		1/2			P	HP:probinson[2021-10-31]
OMIM:108950	Atrial tachyarrhythmia with short pr interval		HP:0004754	OMIM:108950	PCS					P	HPO:probinson[2012-04-09]
OMIM:108950	Atrial tachyarrhythmia with short pr interval		HP:0006671	OMIM:108950	PCS					P	HPO:probinson[2012-04-09]
OMIM:108950	Atrial tachyarrhythmia with short pr interval		HP:0005165	OMIM:108950	PCS					P	HPO:probinson[2012-04-09]
OMIM:108950	Atrial tachyarrhythmia with short pr interval		HP:0004757	OMIM:108950	PCS					P	HPO:probinson[2012-04-09]
OMIM:108950	Atrial tachyarrhythmia with short pr interval		HP:0000006	OMIM:108950	PCS					I	HPO:probinson[2012-04-09]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0005216	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0030975	OMIM:614688	TAS					P	HPO:probinson[2018-03-05]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0010628	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0000486	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001310	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001250	OMIM:614688	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001252	OMIM:614688	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001251	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001290	OMIM:614688	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0012155	OMIM:614688	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001508	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0000639	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0002937	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0000657	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0002835	OMIM:614688	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0003745	OMIM:614688	TAS					I	HPO:skoehler[2015-12-30]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0002599	OMIM:614688	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001249	OMIM:614688	TAS		HP:0040281			P	HPO:skoehler[2012-11-20]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001347	PMID:21651769	PCS		3/3			P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0002015	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001344	OMIM:614688	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0002650	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0000496	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0002079	OMIM:614688	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0011968	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0001263	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0011448	OMIM:614688	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0000902	OMIM:614688	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0000407	OMIM:614688	TAS					P	HPO:iea[2017-05-27]
OMIM:614688	Pontine tegmental cap dysplasia		HP:0000508	OMIM:614688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0002663	PMID:7670472	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0003301	OMIM:132400	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0003510	OMIM:132400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0005743	OMIM:132400	TAS					P	HPO:probinson[2012-07-28]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0006429	OMIM:132400	TAS					P	HPO:probinson[2012-06-08]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0002761	OMIM:132400	TAS					P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0001387	OMIM:132400	TAS					P	HPO:skoehler[2010-06-20]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0003300	OMIM:132400	TAS					P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0030840	PMID:7670472	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0010049	OMIM:132400	TAS					P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0010585	OMIM:132400	TAS					P	HPO:probinson[2012-06-18]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0100864	OMIM:132400	TAS					P	HPO:probinson[2012-06-08]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0010582	PMID:7670472	PCS		1/1			P	HPO:probinson[2012-06-18];HPO:probinson[2022-08-07]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0008873	OMIM:132400	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0002515	OMIM:132400	TAS					P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0002857	OMIM:132400	TAS					P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0002656	PMID:7670472	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0008800	PMID:7670472	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0008843	OMIM:132400	TAS					P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0001763	PMID:7670472	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0000006	PMID:7670472	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0009803	OMIM:132400	TAS					P	HPO:probinson[2009-02-17]
OMIM:132400	Epiphyseal dysplasia, multiple, 1		HP:0003502	PMID:7670472	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:614850	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6		HP:0011463	PMID:22105173	PCS		3/3			C	HPO:probinson[2023-04-22];HPO:probinson[2023-04-22]
OMIM:614850	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6		HP:0003829	PMID:22105173	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-22]
OMIM:614850	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6		HP:0000007	PMID:22105173	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-04-22]
OMIM:614850	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6		HP:0012302	PMID:22105173	PCS		3/5			P	HPO:probinson[2013-08-10];HPO:probinson[2023-04-22]
OMIM:614850	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6		HP:0012302	PMID:26513235	PCS	HP:0003584	2/2			P	HPO:probinson[2023-04-22]
OMIM:614850	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6		HP:0000006	PMID:22105173	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-04-22]
OMIM:614850	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 6		HP:0011107	PMID:22105173	PCS		3/5			P	HPO:probinson[2023-04-22]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0000252	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0011968	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0001508	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0001272	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0001250	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0001263	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0001252	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0003593	PMID:23842455	PCS		2/2			C	HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0000007	PMID:23842455	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0012345	PMID:23842455	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-27]
OMIM:615596	Congenital disorder of glycosylation, type Iw		HP:0001249	PMID:23842455	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-27]
OMIM:141405	Hemifacial spasm, familial		HP:0000707	OMIM:141405	IEA					P	HPO:iea[2009-02-17]
OMIM:141405	Hemifacial spasm, familial		HP:0010828	OMIM:141405	TAS					P	HPO:skoehler[2012-10-17]
OMIM:141405	Hemifacial spasm, familial		HP:0000006	OMIM:141405	IEA					I	HPO:iea[2009-02-17]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000286	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0010804	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0007814	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000343	OMIM:614105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0002188	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0001332	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000463	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0003196	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0001252	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0003593	PMID:23835272	PCS		1/1			C	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0045034	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0033725	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0008070	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:6000219	PMID:23835272	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000518	OMIM:614105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0010055	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0007165	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0040155	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000954	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000316	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000414	OMIM:614105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0002912	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000218	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0001942	OMIM:614105	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000252	OMIM:614105	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000494	OMIM:614105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0006956	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0002079	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0011968	OMIM:614105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0002151	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0001263	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0005280	OMIM:614105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:6000607	PMID:21863277	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0012120	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0020079	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000568	OMIM:614105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000348	PMID:23835272	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000007	PMID:23835272	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0002007	PMID:23835272	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:614105	Methylmalonate semialdehyde dehydrogenase deficiency		HP:0000322	PMID:23835272	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:614111	Pyruvate dehydrogenase E1-beta deficiency		HP:0001265	PMID:15138885	PCS		1/2			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:614111	Pyruvate dehydrogenase E1-beta deficiency		HP:0001274	PMID:15138885	PCS		1/2			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:614111	Pyruvate dehydrogenase E1-beta deficiency		HP:0001263	PMID:15138885	PCS					P	HPO:probinson[2020-07-20]
OMIM:614111	Pyruvate dehydrogenase E1-beta deficiency		HP:0001290	PMID:15138885	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:614111	Pyruvate dehydrogenase E1-beta deficiency		HP:0000007	PMID:15138885	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:614111	Pyruvate dehydrogenase E1-beta deficiency		HP:0001987	PMID:15138885	PCS					P	HPO:probinson[2020-07-20]
OMIM:614111	Pyruvate dehydrogenase E1-beta deficiency		HP:0003128	PMID:15138885	PCS	HP:0003623	2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0002069	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000486	PMID:33894126	PCS		5/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0004322	PMID:33894126	PCS		3/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001252	PMID:33894126	PCS		8/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001251	PMID:33894126	PCS		3/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0025101	PMID:33894126	PCS		2/3			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0004283	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0008491	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000718	PMID:33894126	PCS		4/7			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0012471	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000316	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0025336	PMID:33894126	PCS		8/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001385	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000054	PMID:33894126	PCS		2/3	MALE		P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000494	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001344	PMID:33894126	PCS		6/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001382	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000490	PMID:33894126	PCS		2/6			P	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0002072	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001182	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0010952	PMID:33894126	PCS	HP:0011461	1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000729	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0002827	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000601	PMID:33894126	PCS		2/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000400	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0002305	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0007359	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000322	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000520	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000006	PMID:33894126	PCS					I	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000248	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000189	PMID:33894126	PCS		2/6			P	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001274	PMID:33894126	PCS		8/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0009487	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000733	PMID:33894126	PCS		2/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001305	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000218	PMID:33894126	PCS		2/6			P	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000154	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0002212	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0002015	PMID:33894126	PCS		6/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0002650	PMID:33894126	PCS		5/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000431	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0031936	PMID:33894126	PCS		8/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001321	PMID:33894126	PCS		6/7			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0003066	PMID:33894126	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0011344	PMID:33894126	PCS		8/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0100710	PMID:33894126	PCS		1/7			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0031061	PMID:33894126	PCS		8/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001558	PMID:33894126	PCS	HP:0011461	2/8			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0001357	PMID:33894126	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619435	Ritscher-Schinzel syndrome 4		HP:0000028	PMID:33894126	PCS		1/3	MALE		P	HPO:probinson[2021-08-21]
OMIM:179830	Renal tubular acidosis, proximal		HP:0004322	PMID:888846	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:179830	Renal tubular acidosis, proximal		HP:0002748	PMID:888846	PCS		0/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:179830	Renal tubular acidosis, proximal		HP:0002150	PMID:888846	PCS		0/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:179830	Renal tubular acidosis, proximal		HP:0002749	PMID:888846	PCS		0/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:179830	Renal tubular acidosis, proximal		HP:0001995	PMID:888846	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:179830	Renal tubular acidosis, proximal		HP:0002049	PMID:888846	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:179830	Renal tubular acidosis, proximal		HP:0000006	PMID:888846	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2024-03-08]
OMIM:179830	Renal tubular acidosis, proximal		HP:0003259	PMID:888846	PCS		0/9			P	HPO:probinson[2024-03-08]
OMIM:610377	Mevalonic aciduria		HP:0003236	PMID:2850914;PMID:12563048	PCS		4/4			P	HPO:probinson[2020-11-01];HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0032638	PMID:2850914;PMID:12563048;PMID:8352861	PCS		7/7			P	HPO:probinson[2020-11-01];HPO:probinson[2020-03-14];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001531	PMID:8352861	PCS	HP:0003593	3/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0004322	PMID:12563048	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001252	PMID:12563048	PCS		2/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001252	PMID:2850914	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001251	PMID:2850914;PMID:12563048	PCS		4/4			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0003593	PMID:8352861	PCS		3/3			C	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001290	PMID:12563048	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000518	PMID:8352861	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000639	OMIM:610377	TAS					P	HPO:iea[2009-02-17]
OMIM:610377	Mevalonic aciduria		HP:0000239	PMID:16722536	PCS	HP:0003577				P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0007843	PMID:12563048	PCS		3/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002335	OMIM:610377	TAS					P	HPO:iea[2009-02-17]
OMIM:610377	Mevalonic aciduria		HP:0000358	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0003565	PMID:12563048	PCS		2/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002751	PMID:12563048	PCS		2/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000494	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000252	PMID:8352861	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001260	PMID:12563048	PCS		1/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001263	PMID:12563048;PMID:8352861	PCS		16/16			P	HPO:skoehler[2019-02-22];HPO:probinson[2020-11-01];HPO:probinson[2020-11-01];HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002073	OMIM:610377	TAS	HP:0011463				P	HPO:iea[2009-02-17]
OMIM:610377	Mevalonic aciduria		HP:6000606	OMIM:610377	TAS					P	HPO:probinson[2024-05-09]
OMIM:610377	Mevalonic aciduria		HP:0100018	PMID:12563048	PCS		2/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002829	PMID:12563048	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000969	PMID:12563048	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000007	PMID:16835861	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0006268	OMIM:610377	TAS					P	HPO:iea[2009-02-17]
OMIM:610377	Mevalonic aciduria		HP:0000369	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000325	PMID:8352861	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001974	PMID:12563048	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001272	PMID:12563048	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001508	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002719	PMID:8352861	PCS		3/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001903	PMID:8352861	PCS		3/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0004819	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002716	PMID:12563048	PCS		2/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0025435	PMID:2850914	PCS		1/1			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002910	PMID:2850914	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002014	PMID:12563048	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0410246	PMID:12563048	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002059	PMID:8352861	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000430	PMID:8352861	PCS		2/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0002013	PMID:12563048	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000592	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0011227	PMID:12563048	PCS		2/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0012282	PMID:16722536	PCS					P	HPO:skoehler[2013-04-18];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0006564	OMIM:610377	TAS					P	HPO:iea[2009-02-17]
OMIM:610377	Mevalonic aciduria		HP:0000988	PMID:12563048	PCS		2/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000268	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0000543	PMID:12563048	PCS		1/3			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001433	PMID:12563048;PMID:8352861	PCS		5/6			P	HPO:probinson[2020-11-01]
OMIM:610377	Mevalonic aciduria		HP:0001873	PMID:16722536	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-01]
OMIM:166910	Ovalocytosis, hereditary hemolytic, with defective erythropoiesis		HP:0004445	OMIM:166910	TAS					P	HPO:probinson[2009-02-17]
OMIM:166910	Ovalocytosis, hereditary hemolytic, with defective erythropoiesis		HP:0001878	OMIM:166910	TAS					P	HPO:probinson[2009-02-17]
OMIM:166910	Ovalocytosis, hereditary hemolytic, with defective erythropoiesis		HP:0010972	OMIM:166910	TAS					P	HPO:probinson[2009-02-17]
OMIM:166910	Ovalocytosis, hereditary hemolytic, with defective erythropoiesis		HP:0000006	OMIM:166910	TAS					I	HPO:probinson[2009-02-17]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0003593	OMIM:147060	IEA					C	HPO:iea[2009-02-17]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002020	PMID:28803389	PCS		29/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0410151	PMID:28803389	PCS		11/17			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000280	OMIM:147060	IEA					P	HPO:iea[2009-02-17]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0033842	PMID:28803389	PCS		7/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0031984	PMID:28803389	PCS		9/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0032043	PMID:28803389	PCS		4/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0011220	PMID:18978467	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-26]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000316	OMIM:147060	IEA					P	HPO:iea[2009-02-17]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002018	PMID:28803389	PCS		13/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002019	PMID:28803389	PCS		10/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0005425	OMIM:147060	TAS					P	HPO:probinson[2009-02-17]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0410147	PMID:28803389	PCS		7/14			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002035	PMID:28803389	PCS		2/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0001382	PMID:17676033;PMID:33717144;PMID:20159255	PCS		39/90			P	HPO:iea[2009-02-17];HP:probinson[2019-04-08];HPO:probinson[2024-03-18];HPO:probinson[2022-04-01];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002592	PMID:28803389	PCS		4/23			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0032445	PMID:20159255	PCS		47/63			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0009098	PMID:20159255	PCS		25/58			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000964	PMID:17676033;PMID:33717144;PMID:20159255	PCS		76/99			P	HPO:probinson[2022-04-01];HPO:probinson[2024-03-18];HPO:probinson[2009-02-17];HP:probinson[2019-04-08];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002788	PMID:20159255	PCS		27/59			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000006	PMID:17881745	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002027	PMID:28803389	PCS		17/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002588	PMID:28803389	PCS		3/23			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000445	PMID:17676033	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0011919	PMID:33717144	PCS		3/27			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0003212	PMID:17676033;PMID:33717144;PMID:28803389	PCS		99/105			P	HPO:probinson[2012-06-08];HP:probinson[2019-04-08];HPO:probinson[2024-03-18];HPO:probinson[2022-04-01];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002043	PMID:28803389	PCS		2/23			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0010783	OMIM:147060	IEA					P	HPO:skoehler[2018-10-08]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0031368	PMID:28803389	PCS		4/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0031292	PMID:17676033;PMID:33717144	PCS		29/35		HP:0031796	P	HPO:probinson[2022-04-01];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0033351	PMID:28803389	PCS		4/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000938	OMIM:147060	IEA					P	HPO:iea[2009-02-17]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002757	PMID:20159255	PCS		27/59			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0100749	PMID:28803389	PCS		6/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0100628	PMID:28803389	PCS		2/23			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000218	PMID:17676033;PMID:20159255	PCS		31/61			P	HPO:probinson[2024-03-18];HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0006532	PMID:17676033;PMID:20159255	PCS		68/72			P	HP:probinson[2019-04-08];HPO:probinson[2024-03-18];HPO:probinson[2022-04-01]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0006335	PMID:17676033;PMID:20159255	PCS		47/63			P	HPO:probinson[2024-03-18];HPO:probinson[2012-06-08];HP:probinson[2019-04-08];HPO:probinson[2022-04-01]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002014	PMID:28803389	PCS		5/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0001363	PMID:18978467	PCS		HP:0040283			P	HPO:probinson[2009-02-17];HP:probinson[2019-04-08]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0001880	PMID:17676033;PMID:33717144;PMID:20159255	PCS		65/93			P	HPO:iea[2009-02-17];HP:probinson[2019-04-08];HPO:probinson[2024-03-18];HPO:probinson[2022-04-01];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002015	PMID:28803389	PCS		22/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002650	PMID:17676033;PMID:33717144;PMID:20159255	PCS		17/85			P	HPO:iea[2009-02-17];HP:probinson[2019-04-08];HPO:probinson[2022-04-01];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0031858	PMID:28803389	PCS		1/23			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002253	PMID:28803389	PCS		2/70			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0004791	PMID:28803389	PCS		6/23			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0031141	PMID:28803389	PCS		6/25			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002728	PMID:17676033;PMID:33717144	PCS		17/35			P	HP:probinson[2019-04-08];HPO:probinson[2022-04-01];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002726	PMID:17881745	PCS					P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-08]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0000988	PMID:20159255	PCS	HP:0003623	37/57			P	HP:probinson[2019-04-08];HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0100838	PMID:20159255	PCS		58/64			P	HPO:probinson[2024-03-18]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002007	OMIM:147060	IEA					P	HPO:iea[2009-02-17]
OMIM:147060	Hyper-IgE recurrent infection syndrome		HP:0002841	OMIM:147060	TAS					P	HPO:probinson[2012-06-08]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0000252	PMID:11889465	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0000750	PMID:11889465	PCS		6/8			P	HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0011463	PMID:11889465	PCS					C	HPO:probinson[2021-08-30];HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0000729	PMID:11889465	PCS		1/8			P	HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0000729	PMID:12525535	PCS		1/4	MALE		P	HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0001252	PMID:11889465	PCS	HP:0011463	2/8			P	HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0000739	PMID:11889465	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0001423	PMID:11889465	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0001249	PMID:11889465	PCS		8/8			P	HPO:probinson[2013-02-24];HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0001249	PMID:12525535	PCS		4/4	MALE		P	HPO:probinson[2021-08-30]
OMIM:300387	Intellectual developmental disorder, X-linked 63		HP:0001347	PMID:11889465	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-30]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0033393	PMID:36796361	PCS		5/5			P	HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0034011	PMID:36796361	PCS		6/6			P	HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0032560	PMID:36796361	PCS		5/5			P	HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0003251	PMID:36796361	PCS		6/6			P	HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0011462	PMID:36796361	PCS		6/6			C	HPO:probinson[2023-06-17];HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0012207	PMID:36796361	PCS		6/6			P	HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0001417	PMID:36796361	PCS					I	HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0032558	PMID:36796361	PCS		3/5			P	HPO:probinson[2023-06-17];HPO:probinson[2023-06-17]
OMIM:301099	Spermatogenic failure, X-linked, 5		HP:0032559	PMID:36796361	PCS		5/5			P	HPO:probinson[2023-06-17]
OMIM:609140	Corneal dystrophy, posterior polymorphous, 2		HP:0007957	OMIM:609140	TAS					P	HPO:probinson[2013-03-26]
OMIM:609140	Corneal dystrophy, posterior polymorphous, 2		HP:0001131	OMIM:609140	TAS					P	HPO:probinson[2013-03-26]
OMIM:609140	Corneal dystrophy, posterior polymorphous, 2		HP:0000006	OMIM:609140	TAS					I	HPO:probinson[2013-01-09]
OMIM:613118	Antithrombin III deficiency		HP:0040226	PMID:6582486	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:613118	Antithrombin III deficiency		HP:0025324	OMIM:613118	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613118	Antithrombin III deficiency		HP:0000007	PMID:6582486	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613118	Antithrombin III deficiency		HP:0001976	PMID:3055413	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613118	Antithrombin III deficiency		HP:0002625	PMID:3055413	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613118	Antithrombin III deficiency		HP:0004419	PMID:6582486	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-19]
OMIM:613118	Antithrombin III deficiency		HP:0000006	PMID:3055413	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613118	Antithrombin III deficiency		HP:0005305	OMIM:613118	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613118	Antithrombin III deficiency		HP:0002204	OMIM:613118	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0002421	PMID:29727687	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000286	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0003676	PMID:29727687	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0003577	PMID:29727687	IEA		2/3			C	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000640	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001250	PMID:29727687	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001371	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0002120	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001272	PMID:29727687	PCS		1/3		HP:0003676	P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001290	PMID:29727687	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0002380	PMID:29727687	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0012389	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001508	PMID:29727687	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0011461	PMID:29727687	PCS		1/3			C	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0007002	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000316	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001308	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000218	PMID:29727687	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0025116	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001324	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001348	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001347	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0003700	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001562	OMIM:618065	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001265	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0008936	PMID:29727687	PCS		2/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000252	PMID:29727687	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0003324	PMID:29727687	PCS		2/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0006934	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0002059	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0011968	PMID:29727687	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001263	PMID:29727687	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000470	OMIM:618065	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0002093	PMID:29727687	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001181	PMID:29727687	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0002828	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0200136	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001999	OMIM:618065	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001558	PMID:29727687	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000007	PMID:29727687	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0002205	PMID:29727687	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001511	OMIM:618065	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000565	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001257	PMID:29727687	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0001612	PMID:29727687	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-26]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000369	OMIM:618065	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618065	Pontocerebellar hypoplasia, type 1D		HP:0000666	PMID:29727687	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0003577	PMID:15146459	PCS		1/1			C	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0001476	OMIM:614887	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0001250	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0001252	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0002240	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0003593	PMID:15146459;PMID:18285423	PCS		2/2			C	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0001290	PMID:18285423	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0002282	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0033643	PMID:15146459	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0031964	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0006571	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000239	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0001406	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000952	PMID:18285423	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0008936	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0005469	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0031956	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000431	PMID:15146459	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0011968	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0001284	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0005280	PMID:15146459	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0002908	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000627	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000007	PMID:15146459	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000348	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000268	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0003811	PMID:15146459	PCS		1/1			C	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0003215	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000347	PMID:15146459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0002126	PMID:18285423	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:614887	Peroxisome biogenesis disorder 13A (Zellweger)		HP:0000325	PMID:15146459	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-06]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0002751	PMID:23956177	PCS		3/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000252	PMID:23956177	PCS		3/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000340	PMID:23956177	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000750	PMID:23956177	PCS		3/3		HP:0012828	P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000486	OMIM:615541	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0004322	PMID:23956177	PCS		3/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0031936	PMID:23956177	PCS		3/3			P	HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000490	PMID:23956177	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0001263	PMID:23956177	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0003593	PMID:23956177	PCS					C	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0040080	PMID:23956177	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000718	PMID:23956177	PCS		3/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000448	PMID:23956177	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000007	PMID:21937992	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000733	PMID:23956177	PCS		3/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000689	PMID:23956177	PCS		2/3			P	HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0001822	PMID:23956177	PCS		1/3			P	HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000752	PMID:23956177	PCS		3/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000400	PMID:23956177	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:615541	Intellectual developmental disorder, autosomal recessive 39		HP:0000664	PMID:23956177	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2022-02-24]
OMIM:613656	Migraine, with or without aura, susceptibility to, 13		HP:0002077	PMID:20871611	PCS					P	HPO:probinson[2020-07-11]
OMIM:613656	Migraine, with or without aura, susceptibility to, 13		HP:0002083	PMID:20871611	PCS					P	HPO:probinson[2020-07-11]
OMIM:613656	Migraine, with or without aura, susceptibility to, 13		HP:0000006	PMID:20871611	PCS					I	HPO:probinson[2020-07-11];HPO:probinson[2022-12-03]
OMIM:278200	Woolly hair, hypotrichosis, everted lower lip, and outstanding ears		HP:0002224	OMIM:278200	TAS					P	HPO:skoehler[2010-06-18]
OMIM:278200	Woolly hair, hypotrichosis, everted lower lip, and outstanding ears		HP:0000232	OMIM:278200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:278200	Woolly hair, hypotrichosis, everted lower lip, and outstanding ears		HP:0000007	OMIM:278200	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:278200	Woolly hair, hypotrichosis, everted lower lip, and outstanding ears		HP:0000411	OMIM:278200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:278200	Woolly hair, hypotrichosis, everted lower lip, and outstanding ears		HP:0008070	OMIM:278200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0030149	PMID:20551992	PCS		4/15			P	HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0034197	PMID:20551992	PCS		3/15			C	HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0002098	PMID:20551992	PCS		14/15			P	HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0003593	PMID:20551992	PCS		12/15			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0030682	PMID:20551992	PCS		7/15			P	HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0000007	PMID:20551992	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0001635	PMID:20551992	PCS		11/15			P	HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0008314	PMID:20551992	PCS		3/3			P	HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0012664	PMID:20551992	PCS		15/15			P	HPO:probinson[2022-07-03]
OMIM:613642	Cardiomyopathy, dilated, 1GG		HP:0001644	PMID:20551992	PCS		15/15			P	HPO:probinson[2013-06-02];HPO:probinson[2022-07-03]
OMIM:154020	Hypomagnesemia 2, renal		HP:0005567	PMID:25765846	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:154020	Hypomagnesemia 2, renal		HP:0003324	OMIM:154020	TAS					P	HPO:skoehler[2017-07-13]
OMIM:154020	Hypomagnesemia 2, renal		HP:0001250	OMIM:154020	IEA					P	HPO:iea[2009-02-17]
OMIM:154020	Hypomagnesemia 2, renal		HP:0002917	PMID:25765846	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:154020	Hypomagnesemia 2, renal		HP:0000083	OMIM:154020	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:154020	Hypomagnesemia 2, renal		HP:0002900	PMID:25765846	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-14]
OMIM:154020	Hypomagnesemia 2, renal		HP:0000934	OMIM:154020	TAS					P	HPO:skoehler[2017-07-13]
OMIM:154020	Hypomagnesemia 2, renal		HP:0000006	PMID:11062458	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-14]
OMIM:154020	Hypomagnesemia 2, renal		HP:0003127	PMID:25765846	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-14]
OMIM:615233	Retinitis pigmentosa 66		HP:0001133	PMID:19074801	PCS		2/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0007737	PMID:19074801	PCS		2/2			P	HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0000662	PMID:19074801	PCS	HP:0003581	1/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0003581	PMID:19074801	PCS		4/4			C	HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0000007	PMID:19074801	PCS					I	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0007663	PMID:19074801	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0000505	PMID:19074801	PCS		2/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0000603	PMID:19074801	PCS		2/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0000543	PMID:19074801	PCS		1/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0007787	PMID:19074801	PCS		2/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-31]
OMIM:615233	Retinitis pigmentosa 66		HP:0000510	PMID:19074801	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-31]
OMIM:614893	Immunodeficiency 32A		HP:0002840	PMID:21524210	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:614893	Immunodeficiency 32A		HP:0020086	PMID:21524210	PCS		2/2			P	HPO:probinson[2022-11-11]
OMIM:614893	Immunodeficiency 32A		HP:0002719	PMID:21524210	PCS					P	HPO:probinson[2017-06-21]
OMIM:614893	Immunodeficiency 32A		HP:0011463	PMID:21524210	PCS		2/2			C	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614893	Immunodeficiency 32A		HP:0032252	PMID:21524210	PCS		2/2			P	HPO:probinson[2022-11-11]
OMIM:614893	Immunodeficiency 32A		HP:0002716	PMID:21524210	PCS		2/2			P	HPO:probinson[2017-06-21];HPO:probinson[2022-11-11]
OMIM:614893	Immunodeficiency 32A		HP:0001945	PMID:21524210	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:614893	Immunodeficiency 32A		HP:0000006	PMID:21524210	PCS					I	HPO:probinson[2017-06-21]
OMIM:614893	Immunodeficiency 32A		HP:0002721	PMID:21524210	PCS					P	HPO:probinson[2017-06-21]
OMIM:615555	Hyperprolactinemia		HP:0000132	PMID:24195502	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-25]
OMIM:615555	Hyperprolactinemia		HP:0031109	OMIM:615555	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:615555	Hyperprolactinemia		HP:0000870	PMID:24195502	PCS		3/3			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-25]
OMIM:615555	Hyperprolactinemia		HP:0008222	PMID:24195502	PCS		1/3			P	HPO:probinson[2023-02-25]
OMIM:615555	Hyperprolactinemia		HP:0011462	PMID:24195502	PCS		3/3			C	HPO:probinson[2023-02-25]
OMIM:615555	Hyperprolactinemia		HP:0000876	PMID:24195502	PCS		2/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-25]
OMIM:615555	Hyperprolactinemia		HP:0100829	PMID:24195502	PCS		1/3			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615555	Hyperprolactinemia		HP:0000007	OMIM:615555	TAS					I	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-25]
OMIM:615555	Hyperprolactinemia		HP:0000006	PMID:24195502	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-25]
OMIM:186600	Syringomas, multiple		HP:0000006	OMIM:186600	IEA					I	HPO:iea[2009-02-17]
OMIM:186600	Syringomas, multiple		HP:0000951	OMIM:186600	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000286	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0004322	PMID:21378989	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000160	PMID:21378989	PCS		9/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000280	OMIM:102500	TAS					P	HPO:skoehler[2013-11-18]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000316	PMID:21378989	PCS		9/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000238	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0002857	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001643	PMID:21378989	PCS		2/9			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000113	PMID:21378989	PCS		2/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001007	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001249	PMID:21378989	PCS		0/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0009748	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001842	PMID:21378989	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0002751	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000494	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000574	PMID:21378989	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000293	OMIM:102500	TAS					P	HPO:skoehler[2013-11-18]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001382	PMID:21378989	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0005463	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001263	PMID:21378989	PCS		0/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0003083	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0006180	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0009771	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001537	PMID:21378989	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000689	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000527	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000405	PMID:21378989	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000047	PMID:21378989	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000006	PMID:21378989	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000369	PMID:21378989	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000445	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000343	OMIM:102500	IEA		9/9			P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000463	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0004586	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000023	PMID:21378989	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0010502	PMID:21378989	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000939	PMID:21378989	PCS		7/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001508	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001629	PMID:21378989	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000938	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000612	PMID:21378989	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000218	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0002953	PMID:21378989	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0002756	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000272	PMID:21378989	PCS		9/9			P	HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000470	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0006480	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0008462	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000506	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000107	OMIM:102500	IEA					P	HPO:skoehler[2012-10-09]
OMIM:102500	Hajdu-Cheney syndrome		HP:0008421	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000664	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0002645	PMID:21378989	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0005758	PMID:21378989	PCS		5/9			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000028	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0002566	OMIM:102500	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:102500	Hajdu-Cheney syndrome		HP:0000347	PMID:21378989	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:102500	Hajdu-Cheney syndrome		HP:0001799	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:102500	Hajdu-Cheney syndrome		HP:0002688	OMIM:102500	IEA					P	HPO:iea[2009-02-17]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0001561	OMIM:613124	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0002089	OMIM:613124	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0000463	OMIM:613124	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0005257	OMIM:613124	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0001790	OMIM:613124	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0000007	OMIM:613124	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0001789	OMIM:613124	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0000835	OMIM:613124	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613124	Hydrops fetalis, nonimmune, with gracile bones and dysmorphic features		HP:0009824	OMIM:613124	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607151	Moyamoya disease 2, susceptibility to		HP:0000007	PMID:22931863	PCS					I	HPO:probinson[2020-12-04]
OMIM:607151	Moyamoya disease 2, susceptibility to		HP:0011834	PMID:21799892	PCS	HP:0003621	4/4			P	HPO:probinson[2020-12-04];HPO:probinson[2020-12-04]
OMIM:607151	Moyamoya disease 2, susceptibility to		HP:0011834	PMID:22931863	PCS					P	HPO:probinson[2020-12-04]
OMIM:607151	Moyamoya disease 2, susceptibility to		HP:0002326	PMID:22931863	PCS					P	HPO:probinson[2020-12-04]
OMIM:607151	Moyamoya disease 2, susceptibility to		HP:0000006	PMID:21799892	PCS					I	HPO:probinson[2020-12-04];HPO:probinson[2020-12-04]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0000252	PMID:28257693	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0002188	PMID:28257693	PCS		1/2			P	HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0002750	PMID:28257693	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0004322	PMID:28257693	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0001518	PMID:28257693	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0001263	PMID:28257693	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0003593	PMID:28257693	PCS		4/4			C	HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0000007	PMID:28257693	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:617432	Intellectual developmental disorder, autosomal recessive 60		HP:0000823	PMID:28257693	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:150250	Larsen syndrome		HP:0003994	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0007957	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000365	PMID:16801345	PCS		4/19			P	HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0004322	PMID:16801345	PCS		14/20			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0001772	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0002780	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0010049	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0011220	OMIM:150250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:150250	Larsen syndrome		HP:0000316	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0002779	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0002777	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0001249	PMID:16801345	PCS		3/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0003304	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000175	PMID:16801345	PCS		3/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0001222	PMID:16801345	PCS		17/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0003883	PMID:16801345	PCS		3/16			P	HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0001382	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0003042	PMID:16801345	PCS	HP:0003577	13/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0011800	PMID:16801345	PCS		19/20			P	HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0002827	PMID:16801345	PCS	HP:0003577	16/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0002948	PMID:16801345	PCS		8/16			P	HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0006067	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000767	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0002947	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0008127	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000405	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000768	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000006	PMID:14991055	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0000204	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0004568	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0003298	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0012368	OMIM:150250	TAS					P	HPO:skoehler[2013-10-22]
OMIM:150250	Larsen syndrome		HP:0010743	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0001629	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0008434	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0004976	PMID:16801345	PCS	HP:0003577	16/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0002650	PMID:16801345	PCS		12/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0001762	PMID:16801345	PCS		15/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-27]
OMIM:150250	Larsen syndrome		HP:0004232	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0002176	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000272	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0005280	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000668	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0002007	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0001511	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0001631	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000586	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0000028	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0001799	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:150250	Larsen syndrome		HP:0004942	OMIM:150250	IEA					P	HPO:iea[2009-02-17]
OMIM:310800	Nystagmus, myoclonic		HP:0000639	OMIM:310800	IEA					P	HPO:iea[2009-02-17]
OMIM:310800	Nystagmus, myoclonic		HP:0001423	OMIM:310800	IEA					I	HPO:iea[2009-02-17]
OMIM:310800	Nystagmus, myoclonic		HP:0001336	OMIM:310800	IEA					P	HPO:iea[2009-02-17]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0002257	PMID:23349227	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0001036	OMIM:615225	TAS					P	HPO:skoehler[2013-06-06]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0000343	PMID:23349227	PCS		1/1			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0030731	OMIM:615225	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0002860	OMIM:615225	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0000470	PMID:23349227	PCS		1/1			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0025092	OMIM:615225	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0032347	OMIM:615225	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0032107	OMIM:615225	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0006094	PMID:23349227	PCS		1/1			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0032152	OMIM:615225	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0011496	PMID:23349227	PCS		1/1			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0000968	OMIM:615225	IEA					P	HPO:skoehler[2015-01-14]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0011034	OMIM:615225	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0011463	PMID:23349227	PCS		1/1			C	HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0000505	PMID:23349227	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0008404	PMID:23349227	PCS		1/1			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0000982	PMID:23349227	PCS		1/1			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0007502	OMIM:615225	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615225	Palmoplantar carcinoma, multiple self-healing		HP:0000006	PMID:23349227	PCS					I	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:605750	Exudative vitreoretinopathy 3		HP:0000541	OMIM:605750	TAS					P	HPO:skoehler[2015-08-16]
OMIM:605750	Exudative vitreoretinopathy 3		HP:0008052	OMIM:605750	TAS					P	HPO:skoehler[2015-08-16]
OMIM:605750	Exudative vitreoretinopathy 3		HP:0011530	OMIM:605750	TAS					P	HPO:skoehler[2015-10-09]
OMIM:605750	Exudative vitreoretinopathy 3		HP:0007663	OMIM:605750	TAS					P	HPO:skoehler[2015-08-16]
OMIM:605750	Exudative vitreoretinopathy 3		HP:0030490	OMIM:605750	IEA					P	HPO:skoehler[2015-12-30]
OMIM:605750	Exudative vitreoretinopathy 3		HP:0001147	OMIM:605750	TAS					P	HPO:skoehler[2015-08-16]
OMIM:605750	Exudative vitreoretinopathy 3		HP:0000006	OMIM:605750	TAS					I	HPO:skoehler[2015-12-30]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0000572	PMID:9480815	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-29]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0003323	OMIM:614885	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0000365	PMID:9480815	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-29]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0011968	PMID:9480815	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-29]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0000518	OMIM:614885	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0011947	OMIM:614885	IEA					P	HPO:skoehler[2013-01-09]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0011463	PMID:9480815	PCS		1/1			C	HPO:probinson[2023-03-29]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0001252	PMID:9480815	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-29]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0000007	PMID:10441568	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-29]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0001324	PMID:9480815	PCS		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-29]
OMIM:614885	Peroxisome biogenesis disorder 11B		HP:0001433	PMID:9480815	PCS		0/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-29]
OMIM:619379	Spermatogenic failure 54		HP:0030974	PMID:32503832	PCS		1/4			P	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0032560	PMID:32503832	PCS		2/2			P	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0003251	PMID:32503832	PCS		4/4			P	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0011462	PMID:32503832	PCS		4/4			C	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0032562	PMID:32503832	PCS		2/2			P	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0000007	PMID:32503832	PCS					I	HPO:probinson[2021-07-12];HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0012207	PMID:32503832	PCS		4/4			P	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0033524	PMID:32503832	PCS		2/2			P	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0000798	PMID:32503832	PCS		3/4			P	HPO:probinson[2021-07-12]
OMIM:619379	Spermatogenic failure 54		HP:0032559	PMID:32503832	PCS		2/2			P	HPO:probinson[2021-07-12]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0007817	PMID:18412118	PCS					P	HPO:probinson[2020-11-30]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0001250	PMID:18412118	PCS		5/29			P	HPO:probinson[2020-11-30]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0000407	PMID:18412118	PCS		26/29			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-11-30]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0007110	PMID:18412118	PCS		11/29			P	HPO:probinson[2020-11-30]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0002194	PMID:18412118	PCS		21/29			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-11-30]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0000007	PMID:18412118	PCS					I	HPO:probinson[2020-11-30]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0009921	PMID:18412118	PCS					P	HPO:probinson[2020-11-30]
OMIM:601536	Athabaskan brainstem dysgenesis syndrome		HP:0005290	PMID:18412118	PCS		3/4			P	HPO:probinson[2020-11-30]
OMIM:108985	Sveinsson chorioretinal atrophy		HP:0000483	OMIM:108985	IEA					P	HPO:skoehler[2010-06-20]
OMIM:108985	Sveinsson chorioretinal atrophy		HP:0007950	OMIM:108985	IEA					P	HPO:iea[2009-02-17]
OMIM:108985	Sveinsson chorioretinal atrophy		HP:0000006	OMIM:108985	IEA					I	HPO:iea[2009-02-17]
OMIM:108985	Sveinsson chorioretinal atrophy		HP:0000545	OMIM:108985	TAS					P	HPO:probinson[2009-02-17]
OMIM:108985	Sveinsson chorioretinal atrophy		HP:0003677	OMIM:108985	IEA					C	HPO:iea[2009-02-17]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0002069	PMID:29656858	PCS		6/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000483	PMID:29656858	PCS		4/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000486	PMID:29656858	PCS		3/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001651	PMID:29656858	PCS		1/14			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0002266	PMID:29656858	PCS		2/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000540	PMID:29656858	PCS		2/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001250	PMID:29656858	PCS		14/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001252	PMID:29656858	PCS		7/11			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0003593	PMID:29656858	PCS		2/14			C	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0032794	PMID:29656858	PCS		1/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000280	PMID:29656858	PCS		1/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0002280	PMID:29656858	PCS		8/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0011167	PMID:29656858	PCS		2/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000639	PMID:29656858	PCS		3/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001629	PMID:29656858	PCS		1/14			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001903	PMID:29656858	PCS		4/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000316	PMID:29656858	PCS		7/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0020221	PMID:29656858	PCS		2/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000733	PMID:29656858	PCS		6/14			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000219	PMID:29656858	PCS		12/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0002714	PMID:29656858	PCS		9/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000675	PMID:29656858	PCS		3/9			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001249	PMID:29656858	PCS		14/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0003623	PMID:29656858	PCS		12/14			C	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001320	PMID:29656858	PCS		4/14			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000154	PMID:29656858	PCS		9/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0002136	PMID:29656858	PCS		2/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000494	PMID:29656858	PCS		8/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000750	PMID:29656858	PCS		13/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0002133	PMID:29656858	PCS		2/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000431	PMID:29656858	PCS		10/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0031936	PMID:29656858	PCS		8/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000232	PMID:29656858	PCS		5/9			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0010818	PMID:29656858	PCS		1/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001263	PMID:29656858	PCS		14/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000729	PMID:29656858	PCS		4/14			P	HPO:skoehler[2018-10-08]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0032792	PMID:29656858	PCS		2/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0007334	PMID:29656858	PCS		2/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0200134	PMID:29656858	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0004209	PMID:29656858	PCS		3/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000664	PMID:29656858	PCS		4/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001631	PMID:29656858	PCS		1/14			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0007359	PMID:29656858	PCS		4/13			P	HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000006	PMID:29656858	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000028	PMID:29656858	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000545	PMID:29656858	PCS		3/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0001875	PMID:29656858	PCS		2/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:618067	Epileptic encephalopathy, early infantile, 66		HP:0000687	PMID:29656858	PCS		3/9			P	HPO:probinson[2023-03-19]
OMIM:119650	Cleidorhizomelic syndrome		HP:0008905	OMIM:119650	TAS					P	HPO:probinson[2009-02-17]
OMIM:119650	Cleidorhizomelic syndrome		HP:0004220	OMIM:119650	TAS					P	HPO:probinson[2009-02-17]
OMIM:119650	Cleidorhizomelic syndrome		HP:0000889	OMIM:119650	TAS					P	HPO:probinson[2009-02-17]
OMIM:119650	Cleidorhizomelic syndrome		HP:0004209	OMIM:119650	IEA					P	HPO:iea[2009-02-17]
OMIM:119650	Cleidorhizomelic syndrome		HP:0000006	OMIM:119650	IEA					I	HPO:iea[2009-02-17]
OMIM:614891	Immunodeficiency 30		HP:0002719	OMIM:614891	TAS					P	HPO:probinson[2015-05-10]
OMIM:614891	Immunodeficiency 30		HP:0011274	OMIM:614891	TAS					P	HPO:probinson[2015-05-10]
OMIM:614891	Immunodeficiency 30		HP:0000007	OMIM:614891	TAS					I	HPO:probinson[2015-05-10]
OMIM:614891	Immunodeficiency 30		HP:0002721	OMIM:614891	TAS					P	HPO:probinson[2015-05-10]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0003577	OMIM:267450	IEA					C	HPO:skoehler[2010-06-19]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0100598	OMIM:267450	IEA					P	HPO:skoehler[2015-01-26]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0005521	OMIM:267450	IEA					P	HPO:iea[2009-02-17]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0000969	OMIM:267450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0002098	OMIM:267450	IEA					P	HPO:skoehler[2015-01-21]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0002094	OMIM:267450	IEA					P	HPO:skoehler[2010-06-18]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0001426	OMIM:267450	IEA					I	HPO:skoehler[2010-06-19]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0003745	OMIM:267450	IEA					I	HPO:skoehler[2010-06-19]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0100750	OMIM:267450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0002789	OMIM:267450	IEA					P	HPO:skoehler[2010-06-18]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0002643	OMIM:267450	IEA					P	HPO:iea[2009-02-17]
OMIM:267450	Respiratory distress syndrome in premature infants		HP:0001622	OMIM:267450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0003621	PMID:23658386	PCS		2/2			C	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0000970	PMID:20920666	TAS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0003596	PMID:20920666	PCS		1/4			C	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0002166	PMID:23658386	PCS		2/2			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0003431	PMID:23658386	PCS		2/2			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0008959	PMID:23658386	PCS		2/2			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0002460	PMID:20920666	PCS		4/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0012534	PMID:20920666	PCS		1/5			P	HPO:skoehler[2014-02-06];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0009053	PMID:23658386	PCS		2/2		HP:0012828	P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0007141	PMID:20920666	PCS		5/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0007460	PMID:20920666	PCS		1/5			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0033660	PMID:23658386	PCS		1/2			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0007350	PMID:23658386	PCS		2/2			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0011463	PMID:20920666	PCS		1/4			C	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0011462	PMID:20920666	PCS		2/4			C	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0002936	PMID:20920666	PCS		5/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0003409	PMID:20920666	PCS		1/5			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0000006	PMID:20920666	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0200042	PMID:20920666;PMID:23658386	PCS		4/7			P	HPO:probinson[2021-11-24];HPO:skoehler[2012-11-21];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0002754	PMID:20920666	PCS		3/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0007328	PMID:23658386	PCS		2/2			P	HPO:probinson[2021-11-24]
OMIM:613640	Neuropathy, hereditary sensory and autonomic, type IC		HP:0002600	PMID:23658386	PCS		2/2			P	HPO:probinson[2021-11-24]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0000175	PMID:26581901	PCS		1/3			P	HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0000034	PMID:26581901	PCS		1/1	MALE		P	HPO:probinson[2017-06-17];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0010557	PMID:26581901	PCS		1/3			P	HPO:probinson[2017-06-17];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0009295	PMID:26581901	PCS		1/3			P	HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0000407	PMID:26581901	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0001903	PMID:26581901	PCS	HP:0003577	2/3			P	HPO:probinson[2017-06-17];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0006394	PMID:26581901	PCS					P	HPO:probinson[2017-06-17];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0001905	PMID:26581901	PCS	HP:0003577	2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0001789	PMID:26581901	PCS	HP:0011461	1/3			P	HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0001873	PMID:26581901	PCS					P	HPO:probinson[2017-06-17];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0001433	PMID:20091385	PCS		0/1			P	HPO:probinson[2017-06-17];HPO:probinson[2024-03-15]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0000006	PMID:26581901	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0002974	PMID:26581901	PCS		3/3			P	HPO:probinson[2017-06-17];HPO:probinson[2020-11-28]
OMIM:616738	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2		HP:0001875	PMID:26581901	PCS	HP:0003577	1/3			P	HPO:probinson[2017-06-17];HPO:probinson[2020-11-28]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0011939	PMID:18493797	PCS		2/9			P	HPO:probinson[2024-07-22]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0003577	PMID:18493797	PCS		9/9			C	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0001762	PMID:18493797	PCS		2/9			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0001156	PMID:18493797	PCS		3/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0010049	PMID:18493797	PCS		1/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0001171	PMID:18493797	PCS		4/9			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0012385	PMID:18493797	PCS		1/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0012165	PMID:18493797	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0012386	PMID:18493797	PCS		2/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0100257	PMID:18493797	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0009471	PMID:18493797	PCS		2/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0010760	PMID:18493797	PCS		1/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0009276	PMID:18493797	PCS		3/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0009700	PMID:18493797	PCS		1/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0009556	PMID:18493797	PCS		1/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0005736	PMID:18493797	PCS		3/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0000006	PMID:18493797	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0009803	PMID:18493797	PCS		1/9			P	HPO:probinson[2022-10-08]
OMIM:612576	Chromosome 17p13.3, telomeric, duplication syndrome		HP:0001831	PMID:18493797	PCS		1/9			P	HPO:probinson[2022-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0003577	PMID:23240096	PCS		2/4			C	HPO:skoehler[2013-06-05];HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000486	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001250	PMID:23240096	PCS		2/4			P	HPO:skoehler[2013-06-05]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001274	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001252	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0002282	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0030718	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001270	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000414	OMIM:615219	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000238	PMID:23240096	PCS		4/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000612	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0002119	PMID:23240096	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001104	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000256	PMID:23240096	PCS		2/4			P	HPO:skoehler[2015-02-22]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001249	OMIM:615219	TAS					P	HPO:probinson[2015-02-22]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000358	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000494	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000252	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001583	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0030048	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0034197	PMID:23240096	PCS		2/4			C	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000407	OMIM:615219	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001999	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001339	OMIM:615219	IEA		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000007	PMID:23240096	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000648	OMIM:615219	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000505	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001137	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0002007	OMIM:615219	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001631	PMID:23240096	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0001334	OMIM:615219	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0000567	PMID:23240096	PCS		2/4			P	HPO:probinson[2023-06-09]
OMIM:615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies		HP:0009879	OMIM:615219	TAS					P	HPO:probinson[2015-02-22]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000343	OMIM:604314	TAS					P	HPO:probinson[2012-05-01]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000189	OMIM:604314	TAS					P	HPO:skoehler[2013-08-18]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000243	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001250	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000160	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000581	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001252	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0002162	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001290	OMIM:604314	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0006191	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000319	OMIM:604314	TAS					P	HPO:probinson[2012-05-01]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000437	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000414	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0008872	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0009623	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000218	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000059	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0002558	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0005989	OMIM:604314	TAS					P	HPO:skoehler[2015-01-20]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000278	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000311	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000996	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001249	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001601	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000358	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000395	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000252	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001762	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000474	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000391	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000272	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000294	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0011800	OMIM:604314	TAS					P	HPO:skoehler[2013-11-28]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001181	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000807	OMIM:604314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000407	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000506	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001518	OMIM:604314	IEA					P	HPO:skoehler[2019-04-18]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000508	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000007	OMIM:604314	IEA					I	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000403	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000527	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0004209	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000047	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000369	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0001810	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000049	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:604314	Blepharophimosis with facial and genital anomalies and impaired intellectual development		HP:0000269	OMIM:604314	IEA					P	HPO:iea[2009-02-17]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0001276	PMID:20950787	PCS		5/5			P	HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0002169	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0002015	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0002521	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0003676	PMID:20950787	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0002188	PMID:20950787	PCS		5/5			P	HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0002365	PMID:20950787	PCS		5/5			P	HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0011968	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0001250	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0001263	PMID:20950787	PCS		5/5		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0005484	PMID:20950787	PCS		5/5			P	HPO:skoehler[2015-01-27]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0003593	PMID:20950787	PCS		5/5			C	HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0012695	PMID:20950787	PCS		5/5			P	HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0001508	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0002506	PMID:20950787	PCS		5/5		HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0000007	PMID:20950787	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0001257	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-21]
OMIM:613668	Microcephaly, postnatal progressive, with seizures and brain atrophy		HP:0001347	PMID:20950787	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:147710	INTUSSUSCEPTION		HP:0002576	OMIM:147710	IEA					P	HPO:iea[2009-02-17]
OMIM:147710	INTUSSUSCEPTION		HP:0000006	OMIM:147710	IEA					I	HPO:iea[2009-02-17]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003577	PMID:34038740	PCS		2/10			C	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0006989	PMID:34038740	PCS		8/10			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0004840	PMID:34038740	PCS		4/4			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0004322	PMID:34038740	PCS		7/7			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001250	PMID:34038740	PCS		11/11			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001263	PMID:34038740	PCS		12/12			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001252	PMID:34038740	PCS		9/11			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003593	PMID:34038740	PCS		6/10			C	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0005484	PMID:34038740	PCS		9/10			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0002240	PMID:34038740	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003095	PMID:34038740	PCS		2/9			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003270	PMID:34038740	PCS		4/8			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0011227	PMID:34038740	PCS		5/8			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001508	PMID:34038740	PCS		9/9			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003819	PMID:34038740	PCS		2/12			C	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0000007	PMID:34038740	PCS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001954	PMID:34038740	PCS		8/9			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003429	PMID:34038740	PCS		6/7			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001522	PMID:34038740	PCS		7/12			C	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001257	PMID:34038740	PCS		4/7			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003623	PMID:34038740	PCS		2/10			C	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0001369	PMID:34038740	PCS		3/9			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0002754	PMID:34038740	PCS		2/8			P	HPO:probinson[2021-08-22]
OMIM:619423	Combined oxidative phosphorylation deficiency 53		HP:0003700	PMID:34038740	PCS		8/8			P	HPO:probinson[2021-08-22]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0002322	PMID:12244316	PCS		10/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0002067	PMID:12244316	PCS		10/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0001278	PMID:12244316	PCS		2/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0003596	PMID:12244316	PCS		5/12			C	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0001288	PMID:12244316	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0003584	PMID:12244316	PCS		7/12			C	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0002063	PMID:12244316	PCS		10/12			P	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0002172	PMID:12244316	PCS		6/12			P	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0012452	PMID:12244316	PCS		0/12			P	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0000716	PMID:12244316	PCS		1/12			P	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0000738	PMID:12244316	PCS		0/12			P	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0000726	PMID:12244316	PCS		0/12			P	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0002548	PMID:12244316	PCS		8/12			P	HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0002019	PMID:12244316	PCS		6/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0000006	PMID:12244316	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-05-21]
OMIM:616710	Parkinson disease 22, autosomal dominant		HP:0001347	PMID:12244316	PCS		4/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0003577	OMIM:611719	TAS					C	HPO:probinson[2012-05-05]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0030674	OMIM:611719	TAS					C	HPO:skoehler[2017-07-13]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001250	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001252	OMIM:611719	IEA					P	HPO:iea[2009-02-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0012448	OMIM:611719	TAS					P	HPO:skoehler[2013-11-28]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001290	PMID:17873122	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001987	PMID:17873122	PCS		3/3			P	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001522	OMIM:611719	TAS					C	HPO:probinson[2012-05-05]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0005989	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0000278	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001942	OMIM:611719	TAS				HP:0012828	P	HPO:probinson[2012-05-05]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0000358	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0003128	PMID:17873122	PCS		3/3			P	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0008936	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0025672	PMID:17873122	PCS	HP:0034197	3/3			P	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0000252	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0002510	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001541	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0002079	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0011924	PMID:17873122	PCS		1/1			P	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0002352	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0011925	PMID:17873122	PCS		1/1			P	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001263	OMIM:611719	IEA					P	HPO:skoehler[2019-09-07]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0002151	OMIM:611719	IEA					P	HPO:iea[2009-02-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0000091	OMIM:611719	IEA					P	HPO:iea[2009-02-17]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0011923	PMID:17873122	PCS		1/1			P	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0034197	PMID:17873122	PCS		3/3			C	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0000969	OMIM:611719	TAS					P	HPO:probinson[2012-05-05]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001639	OMIM:611719	IEA		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0000007	PMID:17873122	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0008347	PMID:17873122	PCS		1/1			P	HPO:probinson[2023-02-22]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0001510	OMIM:611719	TAS					P	HPO:skoehler[2013-05-31]
OMIM:611719	Combined oxidative phosphorylation deficiency 5		HP:0000369	OMIM:611719	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0003510	PMID:33252156	PCS		5/5			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0002650	PMID:33252156	PCS		3/3			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0001288	PMID:33252156	PCS		5/6			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0003593	PMID:33252156	PCS		6/6			C	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0000280	PMID:33252156	PCS					P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0033985	PMID:33252156	PCS		1/3			P	HPO:probinson[2021-07-16]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0003270	PMID:33252156	PCS		5/6			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0003180	PMID:33252156	PCS		1/3			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0033725	PMID:33252156	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0002937	PMID:33252156	PCS		1/3			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0002827	PMID:33252156	PCS		1/3			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0000943	PMID:33252156	PCS		3/3			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0000007	PMID:33252156	PCS					I	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0002866	PMID:33252156	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0006633	PMID:33252156	PCS		1/3			P	HPO:probinson[2021-06-28]
OMIM:619345	Dysostosis multiplex, Ain-Naz type		HP:0003886	PMID:33252156	PCS		1/3			P	HPO:probinson[2021-06-28]
OMIM:262500	Laron syndrome		HP:0003026	OMIM:262500	TAS	HP:0003593				P	HPO:probinson[2013-12-15]
OMIM:262500	Laron syndrome		HP:0003510	PMID:33912130;PMID:31883394	PCS		4/5			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-06-11];HPO:probinson[2022-06-11]
OMIM:262500	Laron syndrome		HP:0000274	OMIM:262500	IEA					P	HPO:iea[2009-02-17]
OMIM:262500	Laron syndrome		HP:0009826	OMIM:262500	IEA					P	HPO:skoehler[2019-02-22]
OMIM:262500	Laron syndrome		HP:0002750	PMID:33912130	PCS		4/4			P	HPO:probinson[2013-12-15];HPO:probinson[2022-06-11]
OMIM:262500	Laron syndrome		HP:0011463	PMID:31883394	PCS		1/1			C	HPO:probinson[2022-06-11]
OMIM:262500	Laron syndrome		HP:0000592	OMIM:262500	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:262500	Laron syndrome		HP:0030353	PMID:33912130	PCS		4/4			P	HPO:probinson[2022-06-11]
OMIM:262500	Laron syndrome		HP:0012569	OMIM:262500	TAS					P	HPO:probinson[2014-01-08]
OMIM:262500	Laron syndrome		HP:0000007	OMIM:262500	TAS					I	HPO:probinson[2009-02-17]
OMIM:262500	Laron syndrome		HP:0001367	OMIM:262500	IEA					P	HPO:iea[2009-02-17]
OMIM:262500	Laron syndrome		HP:0001620	OMIM:262500	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0001795	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000199	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0001162	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000193	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000691	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0011069	OMIM:258850	TAS					P	HPO:probinson[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0002808	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0010297	OMIM:258850	TAS					P	HPO:skoehler[2017-07-13]
OMIM:258850	Orofaciodigital syndrome III		HP:0000316	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000767	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000007	OMIM:258850	IEA					I	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000414	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000879	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0001830	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0000369	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0001249	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:258850	Orofaciodigital syndrome III		HP:0001336	OMIM:258850	IEA					P	HPO:iea[2009-02-17]
OMIM:614675	Bone marrow failure syndrome 1		HP:0001915	PMID:22541560	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-17]
OMIM:614675	Bone marrow failure syndrome 1		HP:0000407	PMID:22541560	PCS	HP:0003577	4/6			P	HPO:probinson[2022-12-17]
OMIM:614675	Bone marrow failure syndrome 1		HP:0005528	PMID:22541560	PCS		4/6			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-17]
OMIM:614675	Bone marrow failure syndrome 1		HP:0002863	PMID:22541560	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-17]
OMIM:614675	Bone marrow failure syndrome 1		HP:0001876	PMID:22541560	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-17]
OMIM:614675	Bone marrow failure syndrome 1		HP:0000006	PMID:22541560	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-17]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0001562	PMID:25407000;PMID:31427716	PCS		4/4			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0002586	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0000021	PMID:25407000;PMID:29575632	PCS		2/2			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0002089	PMID:25407000	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0010956	PMID:25407000;PMID:29575632;PMID:31427716	PCS		5/5			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0004388	PMID:25407000;PMID:29575632	PCS		2/2			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0002780	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0012727	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0004890	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0004392	PMID:25407000	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0011499	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0003270	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0011102	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0012330	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0033132	PMID:25407000	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0002719	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0000407	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0012383	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0011461	PMID:25407000;PMID:29575632;PMID:31427716	PCS		5/5			C	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0000007	PMID:25407000	PCS					I	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0100519	PMID:25407000	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0001643	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:619351	Megacystis-microcolon-intestinal hypoperistalsis syndrome 2		HP:0004887	PMID:29575632	PCS		1/1			P	HPO:probinson[2021-06-28]
OMIM:151600	Nail disorder, nonsyndromic congenital, 3		HP:0001595	PMID:21665001	PCS		0/25			P	HPO:probinson[2022-11-10]
OMIM:151600	Nail disorder, nonsyndromic congenital, 3		HP:0003577	PMID:21665001	PCS		25/25			C	HPO:probinson[2022-11-10];HPO:probinson[2022-11-10]
OMIM:151600	Nail disorder, nonsyndromic congenital, 3		HP:0011121	PMID:21665001	PCS		0/25			P	HPO:probinson[2022-11-10]
OMIM:151600	Nail disorder, nonsyndromic congenital, 3		HP:0000007	PMID:21665001	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:151600	Nail disorder, nonsyndromic congenital, 3		HP:0001598	OMIM:151600	IEA					P	HPO:iea[2009-02-17]
OMIM:151600	Nail disorder, nonsyndromic congenital, 3		HP:0000006	PMID:21665001	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:151600	Nail disorder, nonsyndromic congenital, 3		HP:0001820	PMID:21665001	PCS		25/25			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-10]
OMIM:183020	Spinal muscular atrophy, segmental		HP:0006802	OMIM:183020	IEA					P	HPO:iea[2009-02-17]
OMIM:183020	Spinal muscular atrophy, segmental		HP:0009130	OMIM:183020	IEA					P	HPO:iea[2009-02-17]
OMIM:183020	Spinal muscular atrophy, segmental		HP:0009037	OMIM:183020	IEA					P	HPO:iea[2009-02-17]
OMIM:183020	Spinal muscular atrophy, segmental		HP:0000006	OMIM:183020	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:618729	Liang-Wang syndrome		HP:0000486	PMID:31152168	PCS		3/9			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000485	PMID:31152168	PCS		1/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0001332	PMID:31152168	PCS		1/8			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0001272	PMID:31152168	PCS		3/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0002121	PMID:31152168	PCS		2/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0001251	PMID:31152168	PCS		3/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0003593	PMID:31152168	PCS					C	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000639	PMID:31152168	PCS		1/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000316	PMID:31152168	PCS		4/5			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000219	PMID:31152168	PCS		4/5			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0002714	PMID:31152168	PCS		4/9			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000158	PMID:31152168	PCS		3/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000675	PMID:31152168	PCS		1/3			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000212	PMID:31152168	PCS		3/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0001601	PMID:31152168	PCS		1/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000699	PMID:31152168	PCS		1/3			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000154	PMID:31152168	PCS		2/5			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0008936	PMID:31152168	PCS		5/8			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000494	PMID:31152168	PCS		4/5			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0002059	PMID:31152168	PCS		2/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000750	PMID:31152168	PCS		7/7			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000431	PMID:31152168	PCS		4/5			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0002133	PMID:31152168	PCS		1/9			P	HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000232	PMID:31152168	PCS		2/4			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000664	PMID:31152168	PCS		1/5			P	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:618729	Liang-Wang syndrome		HP:0000006	PMID:31152168	PCS					I	HPO:probinson[2020-04-28];HPO:probinson[2020-04-28]
OMIM:600166	Hyperparathyroidism, primary, caused by water clear cell hyperplasia		HP:0008200	OMIM:600166	IEA					P	HPO:iea[2009-02-17]
OMIM:600166	Hyperparathyroidism, primary, caused by water clear cell hyperplasia		HP:0000006	OMIM:600166	IEA					I	HPO:iea[2009-02-17]
OMIM:619437	Immunodeficiency 84		HP:0020072	PMID:34155405	PCS		1/3			P	HPO:probinson[2021-08-21]
OMIM:619437	Immunodeficiency 84		HP:0002718	PMID:34155405	PCS		2/3			P	HPO:probinson[2021-08-21]
OMIM:619437	Immunodeficiency 84		HP:0012191	PMID:34155405	PCS	HP:0011462	2/3			P	HPO:probinson[2021-08-21]
OMIM:619437	Immunodeficiency 84		HP:0009789	PMID:34155405	PCS	HP:0011463	1/3			P	HPO:probinson[2021-08-21]
OMIM:619437	Immunodeficiency 84		HP:0010976	PMID:34155405	PCS		3/3			P	HPO:probinson[2021-08-21]
OMIM:619437	Immunodeficiency 84		HP:0000006	PMID:34155405	PCS					I	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619437	Immunodeficiency 84		HP:0001744	PMID:34155405	PCS	HP:0003581	1/3			P	HPO:probinson[2021-08-21]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003431	PMID:7693129	PCS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003376	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0001178	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003693	OMIM:118200;PMID:7693129	PCS		30/30			P	HPO:probinson[2009-02-17];HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0002460	PMID:7693129	PCS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003690	OMIM:118200	TAS					P	HPO:skoehler[2012-11-16]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0001171	OMIM:118200	TAS					P	HPO:skoehler[2015-12-30]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0012074	OMIM:118200	TAS					P	HPO:skoehler[2013-02-25]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0009027	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0002936	PMID:7693129	PCS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003449	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0001765	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0001265	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0002751	OMIM:118200	PCS		HP:0040282			P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0004336	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003587	OMIM:118200	IEA					C	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003621	OMIM:118200	PCS					C	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0001761	PMID:7693129	PCS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003383	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0001284	OMIM:118200;PMID:7693129	TAS		30/30			P	HPO:probinson[2022-05-29];HPO:skoehler[2012-10-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003382	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003380	OMIM:118200	IEA					P	HPO:probinson[2009-02-17]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0011096	OMIM:118200	PCS		HP:0040282			P	HPO:probinson[2012-04-11]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0009830	OMIM:118200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0000006	PMID:7693129	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-15];HPO:probinson[2022-05-29]
OMIM:118200	Charcot-Marie-Tooth disease, type 1B		HP:0003677	OMIM:118200	IEA					C	HPO:probinson[2009-02-17]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0025342	OMIM:107320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0025188	OMIM:107320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0000572	OMIM:107320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0000541	OMIM:107320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0001101	OMIM:107320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0004420	OMIM:107320	IEA					P	HPO:iea[2009-02-17]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0000491	OMIM:107320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0025343	OMIM:107320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0011531	OMIM:107320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0100532	OMIM:107320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0004936	OMIM:107320	IEA					P	HPO:iea[2009-02-17]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0001973	OMIM:107320	IEA					P	HPO:iea[2009-02-17]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0000006	OMIM:107320	IEA					I	HPO:iea[2009-02-17]
OMIM:107320	Antiphospholipid syndrome, familial		HP:0000622	OMIM:107320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:239510	Hyperprolinemia, type II		HP:0003137	OMIM:239510	IEA					P	HPO:iea[2009-02-17]
OMIM:239510	Hyperprolinemia, type II		HP:0001250	OMIM:239510	IEA					P	HPO:skoehler[2010-06-20]
OMIM:239510	Hyperprolinemia, type II		HP:6000620	PMID:9700195	PCS					P	HPO:probinson[2024-04-03]
OMIM:239510	Hyperprolinemia, type II		HP:6000694	OMIM:239510	TAS					P	HPO:probinson[2024-08-04]
OMIM:239510	Hyperprolinemia, type II		HP:6000695	PMID:2624476	PCS		5/5			P	HPO:probinson[2024-05-09]
OMIM:239510	Hyperprolinemia, type II		HP:0000007	OMIM:239510	IEA					I	HPO:iea[2009-02-17]
OMIM:239510	Hyperprolinemia, type II		HP:0008358	OMIM:239510	IEA					P	HPO:iea[2009-02-17]
OMIM:239510	Hyperprolinemia, type II		HP:0003080	OMIM:239510	IEA					P	HPO:iea[2009-02-17]
OMIM:239510	Hyperprolinemia, type II		HP:0003108	OMIM:239510	IEA					P	HPO:iea[2009-02-17]
OMIM:239510	Hyperprolinemia, type II		HP:0001249	OMIM:239510	IEA					P	HPO:iea[2009-02-17]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001199	PMID:19061985	PCS					P	HPO:probinson[2013-03-01]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000365	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000085	PMID:19061985	PCS		HP:0040283			P	HPO:probinson[2013-03-01]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0010487	PMID:19061985	PCS					P	HPO:probinson[2013-03-01]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000939	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001629	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0002719	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000938	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000912	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0025116	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001643	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000413	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000076	PMID:19061985	PCS		HP:0040283			P	HPO:probinson[2013-03-01]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000175	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001561	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000453	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0002650	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001684	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0100512	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0100633	OMIM:612562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001636	PMID:19061985	PCS		HP:0040283			P	HPO:probinson[2013-03-01]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000403	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0005518	PMID:19061985	PCS					P	HPO:probinson[2013-03-01]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001511	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001972	PMID:19061985	PCS					P	HPO:probinson[2013-01-09]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001510	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0009778	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0000006	PMID:19061985	PCS					I	HPO:probinson[2013-03-01]
OMIM:612562	Diamond-Blackfan anemia 7		HP:0001875	OMIM:612562	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0002421	PMID:11528383	PCS		10/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0004325	PMID:11528383	PCS		16/17			P	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0010628	PMID:11528383	PCS		15/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003577	PMID:11528383	PCS		3/17			C	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0004322	PMID:11528383	PCS		16/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001371	OMIM:602771	IEA					P	HPO:iea[2009-02-17]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001252	OMIM:602771	IEA					P	HPO:iea[2009-02-17]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0005991	PMID:11528383	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003593	PMID:11528383	PCS		11/17			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001290	OMIM:602771	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001270	PMID:11528383	PCS		5/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0100297	PMID:11528383	PCS		8/8			P	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001508	PMID:11528383	PCS		16/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001547	OMIM:602771	IEA					P	HPO:iea[2009-02-17]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0000218	OMIM:602771	IEA					P	HPO:iea[2009-02-17]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003803	PMID:11528383	PCS		8/8			P	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003327	OMIM:602771	IEA					P	HPO:iea[2009-02-17]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003789	PMID:11528383	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001620	PMID:11528383	PCS					P	HPO:probinson[2013-04-12];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0002877	PMID:11528383	PCS		10/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003306	PMID:11528383	PCS		7/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003787	PMID:11528383	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001249	PMID:11528383	PCS		0/17			P	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003700	OMIM:602771	IEA					P	HPO:iea[2009-02-17]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003623	PMID:11528383	PCS		3/17			C	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003722	PMID:11528383	PCS		17/17			P	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003324	OMIM:602771	IEA					P	HPO:iea[2009-02-17]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003687	PMID:11528383	PCS		8/8			P	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0002650	PMID:11528383	PCS		16/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0031936	PMID:11528383	PCS		4/17			P	HPO:probinson[2022-09-09];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0002792	PMID:11528383	PCS		14/14			P	HPO:probinson[2013-12-19];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003560	PMID:11528383	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0002091	PMID:11528383	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0000007	PMID:11528383	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0002505	PMID:11528383	PCS		1/17			P	HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0003557	PMID:11528383	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-09]
OMIM:602771	Rigid spine muscular dystrophy 1		HP:0001611	OMIM:602771	TAS					P	HPO:probinson[2013-04-12]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0001212	PMID:18060736	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0000750	PMID:18060736	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0001344	PMID:18060736	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0001250	PMID:18060736	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0000490	PMID:18060736	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0011463	PMID:18060736	PCS		2/2			C	HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0001263	PMID:18060736	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0009797	PMID:18060736	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0011800	PMID:18060736	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0000336	PMID:18060736	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0001249	PMID:18060736	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-06-18]
OMIM:614113	Intellectual developmental disorder, autosomal dominant 2		HP:0000006	PMID:18060736	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-06-18]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0003596	PMID:17186461	PCS		19/23			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0011705	PMID:17186461	PCS		2/18			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0003584	PMID:17186461	PCS		3/13			C	HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0005110	PMID:17186461	PCS		1/18			P	HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0011713	PMID:17186461	PCS		1/18			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0012664	PMID:17186461	PCS		5/18			P	HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0033755	PMID:17186461	PCS		5/18			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0000726	PMID:17186461	PCS		1/18			P	HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0001635	PMID:17186461	PCS		3/18			P	HPO:probinson[2012-07-16];HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0001712	PMID:17186461	PCS		2/18			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0025710	PMID:17186461	PCS		1/13			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0001279	PMID:17186461	PCS		1/18			P	HPO:probinson[2012-07-16];HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0000006	PMID:17186461	PCS					I	HPO:probinson[2012-07-16];HPO:probinson[2022-07-03]
OMIM:613697	Cardiomyopathy, dilated, 1V		HP:0001644	PMID:17186461	PCS		5/16			P	HPO:probinson[2012-07-16];HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:616937	Thrombocytopenia 6		HP:0001892	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0002003	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0000939	OMIM:616937	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616937	Thrombocytopenia 6		HP:0031020	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0000490	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0000601	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0004406	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0001873	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0000006	PMID:26936507	PCS					I	HPO:probinson[2017-06-25]
OMIM:616937	Thrombocytopenia 6		HP:0011974	PMID:26936507	PCS					P	HPO:probinson[2017-06-25]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001254	OMIM:617397	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002202	PMID:27325888	PCS		1/5			P	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001250	PMID:27325888;PMID:31940699	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002240	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001290	OMIM:617397	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002282	PMID:27325888	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0011461	PMID:27325888	PCS		3/5			C	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002119	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0025116	PMID:31940699	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001643	PMID:27325888	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002910	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002514	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0003623	PMID:27325888	PCS		2/5			C	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0003128	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001342	PMID:27325888;PMID:31940699	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0000252	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0006956	PMID:31940699	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001684	PMID:27325888	PCS		1/5			P	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001321	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001662	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001541	PMID:27325888	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0033677	PMID:31940699	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002093	PMID:27325888	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0000007	PMID:27325888	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0000967	PMID:27325888	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0001873	PMID:27325888	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0000883	PMID:27325888	PCS		1/5			P	HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0002126	PMID:27325888	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-23]
OMIM:617397	Pseudo-Torch syndrome 2		HP:0005932	PMID:27325888	PCS		1/5			P	HPO:probinson[2022-03-23]
OMIM:129750	Ectopia pupillae		HP:0009918	OMIM:129750	IEA					P	HPO:skoehler[2015-01-21]
OMIM:129750	Ectopia pupillae		HP:0000006	OMIM:129750	IEA					I	HPO:iea[2009-02-17]
OMIM:614846	Tetrasomy 15q26		HP:0001166	PMID:22653535	PCS		10/12			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0002751	PMID:22653535	PCS		6/11			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000494	PMID:22653535	PCS		8/12			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0003396	PMID:22653535	PCS		1/7			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0001263	PMID:22653535	PCS		7/7			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0001252	PMID:22653535	PCS		4/4			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000085	PMID:22653535	PCS		2/9			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0012304	PMID:22653535	PCS		1/14			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0012385	PMID:22653535	PCS		7/12			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000308	PMID:22653535	PCS		8/11			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000316	PMID:22653535	PCS		8/12			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000238	PMID:22653535	PCS		2/7			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0001305	PMID:22653535	PCS		1/7			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000218	PMID:22653535	PCS		8/8			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0001511	PMID:22653535	PCS		2/14			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000378	PMID:22653535	PCS		1/12			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0001643	PMID:22653535	PCS		1/14			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0001631	PMID:22653535	PCS		1/14			P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000369	PMID:22653535	PCS		7/12			P	HPO:probinson[2023-07-16]
OMIM:614846	Tetrasomy 15q26		HP:0000126	PMID:22653535	PCS		4/9			P	HPO:probinson[2023-07-16]
OMIM:257550	Ocular motor apraxia		HP:0000657	OMIM:257550	IEA					P	HPO:iea[2009-02-17]
OMIM:257550	Ocular motor apraxia		HP:0000007	OMIM:257550	IEA					I	HPO:iea[2009-02-17]
OMIM:257550	Ocular motor apraxia		HP:0008026	OMIM:257550	IEA					P	HPO:iea[2009-02-17]
OMIM:257550	Ocular motor apraxia		HP:0000090	OMIM:257550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257550	Ocular motor apraxia		HP:0006961	OMIM:257550	IEA					P	HPO:iea[2009-02-17]
OMIM:220900	Deafness, congenital, with total albinism		HP:0001022	OMIM:220900	IEA					P	HPO:iea[2009-02-17]
OMIM:220900	Deafness, congenital, with total albinism		HP:0000365	OMIM:220900	IEA					P	HPO:iea[2009-02-17]
OMIM:220900	Deafness, congenital, with total albinism		HP:0000007	OMIM:220900	IEA					I	HPO:iea[2009-02-17]
OMIM:220900	Deafness, congenital, with total albinism		HP:0000135	OMIM:220900	IEA					P	HPO:iea[2009-02-17]
OMIM:220900	Deafness, congenital, with total albinism		HP:0001249	OMIM:220900	IEA					P	HPO:iea[2009-02-17]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0100710	PMID:20598275	PCS		3/3			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0000252	PMID:20598275;PMID:22775483	PCS		5/5			P	HPO:probinson[2022-10-08];HPO:skoehler[2013-06-12];HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0001250	PMID:20598275	PCS		0/3			P	HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0000718	PMID:20598275	PCS		3/3			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0000007	PMID:20598275	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0000722	PMID:20598275	PCS		1/3			P	HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0100716	PMID:22775483	PCS		2/2			P	HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0001335	PMID:20598275	PCS	HP:0003593	3/3			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-10-08]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0009879	PMID:20598275;OMIM:614852	PCS		11/11			P	HPO:probinson[2022-10-08];HPO:skoehler[2014-11-26]
OMIM:614852	Microcephaly 9, primary, autosomal recessive		HP:0100034	PMID:20598275	PCS		1/3			P	HPO:probinson[2022-10-08]
OMIM:617383	Avascular necrosis of femoral head, primary, 2		HP:0005743	PMID:27330106	PCS		4/4			P	HP:probinson[2019-03-09]
OMIM:617383	Avascular necrosis of femoral head, primary, 2		HP:0004322	PMID:27330106	PCS		0/4			P	HP:probinson[2019-03-09];HPO:probinson[2024-03-15]
OMIM:617383	Avascular necrosis of femoral head, primary, 2		HP:0011462	PMID:27330106	PCS		4/4			C	HPO:probinson[2024-03-15]
OMIM:617383	Avascular necrosis of femoral head, primary, 2		HP:0000926	PMID:27330106	PCS		0/4			P	HP:probinson[2019-03-09];HPO:probinson[2024-03-15]
OMIM:617383	Avascular necrosis of femoral head, primary, 2		HP:0000006	PMID:27330106	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0006209	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0001162	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0008079	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0000954	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0004251	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0006210	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0010046	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0001830	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0002986	OMIM:176240	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0000006	OMIM:176240	IEA					I	HPO:iea[2009-02-17]
OMIM:176240	Postaxial oligodactyly, tetramelic		HP:0010579	OMIM:176240	IEA					P	HPO:iea[2009-02-17]
OMIM:156190	Mental and growth retardation with amblyopia		HP:0000646	OMIM:156190	TAS					P	HPO:probinson[2009-02-17]
OMIM:156190	Mental and growth retardation with amblyopia		HP:0001510	OMIM:156190	TAS					P	HPO:probinson[2009-02-17]
OMIM:156190	Mental and growth retardation with amblyopia		HP:0000006	OMIM:156190	TAS					I	HPO:probinson[2009-02-17]
OMIM:156190	Mental and growth retardation with amblyopia		HP:0001249	OMIM:156190	TAS					P	HPO:probinson[2009-02-17]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0003236	PMID:10735275	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0001288	PMID:10735275	PCS		2/2			P	HPO:probinson[2013-02-16];HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0003551	PMID:10735275	PCS		2/2			P	HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0011463	PMID:10735275	PCS		2/2			C	HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0003691	PMID:10735275	PCS		1/1			P	HPO:probinson[2013-02-16];HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0008981	OMIM:601287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0003560	PMID:10735275	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0000007	PMID:8841194	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0007126	PMID:10735275	PCS		1/1			P	HPO:probinson[2013-02-16];HPO:probinson[2022-08-16]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0001714	OMIM:601287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0003391	OMIM:601287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601287	Muscular dystrophy, limb-girdle, type 2F		HP:0003701	PMID:10735275	PCS		1/1			P	HPO:probinson[2013-02-16];HPO:probinson[2022-08-16]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0001771	PMID:22371254	PCS	HP:0011462	3/4			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003236	PMID:29128256	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003577	PMID:36349186	PCS		1/1			C	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003551	PMID:29128256	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0001252	PMID:22371254	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003593	PMID:22371254	PCS		4/4			C	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0012548	PMID:22371254;PMID:29128256	PCS		4/4			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003690	PMID:29128256;PMID:27460346	PCS		2/2			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0001270	PMID:27460346;PMID:36349186	PCS		0/2			P	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0030319	PMID:22371254;PMID:29128256	PCS		5/5			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0100297	PMID:22371254	PCS		3/3			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0040081	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0011463	PMID:29128256;PMID:27460346	PCS		2/2			C	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0032341	PMID:29128256	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003805	PMID:22371254	PCS		0/3			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0002878	PMID:29128256;PMID:27460346	PCS		2/2			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003307	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0000218	PMID:29128256	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0006532	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003327	PMID:22371254	PCS		4/4			P	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003701	PMID:22371254	PCS		4/4			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003789	PMID:27460346	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003787	PMID:22371254	PCS		3/3			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0001249	PMID:27460346;PMID:36349186	PCS		0/2			P	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003722	PMID:29128256	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0008936	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003323	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0000175	PMID:22371254;PMID:36349186	PCS		2/4			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0002015	PMID:29128256;PMID:36349186	PCS		2/2			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003324	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0002650	PMID:22371254	PCS	HP:0011463	4/4			P	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0002650	PMID:27460346	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0002650	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003200	PMID:22371254	PCS		0/3			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0001288	PMID:29128256	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0001284	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0008180	PMID:22371254	PCS		4/4			P	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0034671	PMID:22371254	PCS	HP:0011462	3/4			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0009055	PMID:29128256	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0000007	PMID:22371254	PCS					I	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0034391	PMID:22371254	PCS	HP:0011462	3/4			P	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0034391	PMID:36349186	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0000467	PMID:22371254	PCS	HP:0003593	4/4			P	HPO:probinson[2023-06-25];HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0000467	PMID:22371254	PCS		1/4			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0000467	PMID:27460346	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0001611	PMID:22371254;PMID:29128256	PCS		4/4			P	HPO:probinson[2023-06-25]
OMIM:620249	Congenital myopathy 10B, mild variant		HP:0003557	PMID:27460346	PCS		1/1			P	HPO:probinson[2023-06-25]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0000286	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0003763	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0000252	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0000486	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0001762	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0001773	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0002650	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0001344	OMIM:300434	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0004322	OMIM:300434	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0001250	OMIM:300434	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0001263	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0002020	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0005280	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0002808	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0002827	OMIM:300434	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0000316	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0001417	OMIM:300434	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0000752	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0200055	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300434	Intellectual developmental disorder, X-linked, syndromic, Stocco dos Santos type		HP:0001007	OMIM:300434	TAS					P	HPO:skoehler[2017-07-13]
OMIM:256100	Nephronophthisis 1		HP:0003158	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0003774	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0005576	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0005583	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0000090	PMID:9361039	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-03]
OMIM:256100	Nephronophthisis 1		HP:0000092	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0001959	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0001903	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0000822	OMIM:256100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256100	Nephronophthisis 1		HP:0000007	PMID:9361039	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-03]
OMIM:256100	Nephronophthisis 1		HP:0000108	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0000103	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:256100	Nephronophthisis 1		HP:0001510	OMIM:256100	IEA					P	HPO:iea[2009-02-17]
OMIM:125630	Dermodistortive urticaria		HP:0001025	PMID:26841242	PCS		9/9			P	HPO:skoehler[2012-07-19];HPO:probinson[2024-03-08]
OMIM:125630	Dermodistortive urticaria		HP:0001041	PMID:26841242	PCS		9/9			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-08]
OMIM:125630	Dermodistortive urticaria		HP:0031284	PMID:26841242	PCS		9/9			P	HPO:probinson[2018-03-05]
OMIM:125630	Dermodistortive urticaria		HP:0011971	PMID:26841242	PCS		0/9			P	HPO:probinson[2018-03-05];HPO:probinson[2024-03-08]
OMIM:125630	Dermodistortive urticaria		HP:0000006	PMID:26841242	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0001685	OMIM:613873	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0001639	PMID:17509612	PCS		3/3			P	HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0011462	PMID:17509612	PCS		3/3			C	HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0001681	PMID:17509612	PCS		1/3			P	HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0005110	PMID:17509612	PCS		0/3			P	HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0002094	PMID:17509612	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0001712	PMID:17509612	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0001962	PMID:17509612	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0000006	PMID:17509612	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613873	Cardiomyopathy, familial hypertrophic, 17		HP:0004756	OMIM:613873	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0002136	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0002015	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0003236	PMID:29290614	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0000651	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0001310	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0001272	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0000590	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0001260	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0003584	PMID:29290614	PCS		1/1			C	HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0001251	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0011675	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0011469	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0012663	PMID:29290614	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0000407	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0000508	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0000007	PMID:29290614	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0003701	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0000763	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0003546	PMID:29290614	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618098	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5		HP:0003722	PMID:29290614	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0003577	PMID:36689511;PMID:37212630	PCS		8/8			C	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0001036	PMID:37212630	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0025092	PMID:36689511	PCS					P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0010783	PMID:37212630	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0040189	PMID:36689511	PCS					P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0007431	PMID:36689511	PCS	HP:0003577				P	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0007431	PMID:37212630	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0001019	PMID:37212630	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0001803	PMID:36689511;PMID:37212630	PCS		2/8			P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0000989	PMID:36689511	PCS					P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0000972	PMID:36689511;PMID:37212630	PCS		11/11			P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0007447	PMID:37212630	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0000982	PMID:36689511	PCS					P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0000006	PMID:36689511	PCS					I	HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0000962	PMID:36689511	PCS					P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:620507	Ichthyosis with erythrokeratoderma		HP:0001820	PMID:36689511;PMID:37212630	PCS		2/8			P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0004322	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001332	OMIM:300352	TAS					P	HPO:skoehler[2013-09-10]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001250	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001252	PMID:27408820	PCS		1/3			P	HP:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0003593	OMIM:300352;PMID:27408820	PCS		13/13			C	HPO:probinson[2022-03-09];HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000718	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0002019	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001249	PMID:27408820;PMID:11326334	PCS		3/3			P	HP:probinson[2022-03-09];HPO:probinson[2022-03-09];HPO:skoehler[2012-10-17];HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000098	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000252	PMID:27408820	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0002595	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0002079	OMIM:300352	TAS					P	HPO:skoehler[2013-09-10]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001382	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001263	PMID:27408820;PMID:11326334	PCS		4/4			P	HP:probinson[2022-03-09];HPO:skoehler[2014-04-04];HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0011800	OMIM:300352	TAS					P	HPO:skoehler[2013-11-28]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:6000127	OMIM:300352	TAS					P	HPO:probinson[2024-01-06]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0025051	PMID:27408820;PMID:11326334	PCS		4/4			P	HP:probinson[2022-03-09];HP:probinson[2019-01-27];HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001419	PMID:11326334	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0011098	PMID:27408820	PCS		2/3			P	HP:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001657	PMID:34050321	PCS		7/18			P	HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001257	OMIM:300352	TAS					P	HPO:skoehler[2013-09-10]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001276	PMID:27408820	PCS		1/3			P	HP:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000540	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0012448	OMIM:300352	TAS					P	HPO:skoehler[2013-11-28]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001270	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001508	PMID:27408820	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000733	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0008872	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000337	OMIM:300352	TAS					P	HPO:skoehler[2013-09-10]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000577	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000275	OMIM:300352	TAS					P	HPO:probinson[2012-05-01]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0002058	OMIM:300352	TAS					P	HPO:skoehler[2013-09-10]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0008936	PMID:27408820	PCS		1/3			P	HP:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0002136	PMID:27408820	PCS		1/3			P	HP:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000750	PMID:27408820;PMID:11326334	PCS		2/4			P	HP:probinson[2022-03-09];HPO:iea[2009-02-17];HPO:probinson[2022-03-09]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0002013	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001761	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000276	OMIM:300352	TAS					P	HPO:probinson[2012-05-01]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001288	OMIM:300352	TAS					P	HPO:skoehler[2013-09-10]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000272	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0002251	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0012760	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0008583	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000508	OMIM:300352	TAS					P	HPO:skoehler[2013-09-10]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0007057	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0001319	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0007018	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0000303	OMIM:300352	IEA					P	HPO:iea[2009-02-17]
OMIM:300352	Cerebral creatine deficiency syndrome 1		HP:0034291	PMID:11326334	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0003676	PMID:23746551	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001310	PMID:23746551	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001332	PMID:23746551	PCS		4/18			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0002120	PMID:23746551	PCS		2/10			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001251	PMID:23746551	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0003593	PMID:23746551	PCS		8/18			C	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0002064	OMIM:609195	IEA					P	HPO:iea[2009-02-17]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0002061	PMID:23746551	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0000639	PMID:23746551	PCS		3/18			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0011463	PMID:23746551	PCS		9/18			C	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0007340	PMID:23746551	PCS		14/15			P	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0000712	OMIM:609195	IEA					P	HPO:iea[2009-02-17]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0002359	PMID:23746551	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001347	PMID:23746551	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001265	PMID:23746551	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0002650	PMID:23746551	PCS		10/15			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0003487	PMID:23746551	PCS		14/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001288	PMID:23746551	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001761	PMID:23746551	PCS		9/17			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0000012	OMIM:609195	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0003484	PMID:23746551	PCS		2/15			P	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001260	PMID:23746551	PCS		9/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0002495	PMID:23746551	PCS		8/15			P	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0100020	PMID:23746551	PCS		3/18			P	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0040171	PMID:23746551	PCS		3/13			P	HPO:skoehler[2015-08-05]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0100660	PMID:23746551	PCS		1/18			P	HPO:skoehler[2013-10-06]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0025708	PMID:23746551	PCS		1/18			C	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0000007	PMID:23746551	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0030051	OMIM:609195	TAS					P	HPO:skoehler[2014-11-27]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0001258	PMID:23746551	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0006986	PMID:23746551	PCS		5/15			P	HPO:probinson[2023-03-07]
OMIM:609195	Spastic paraplegia 26, autosomal recessive		HP:0008944	PMID:23746551	PCS		11/18			P	HPO:probinson[2023-03-07]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001254	PMID:33457206;PMID:24498631	PCS		6/6			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001397	PMID:24498631	PCS		2/2			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0003236	PMID:24498631	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0003355	PMID:33457206	PCS		2/2			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001250	PMID:33457206;PMID:24498631	PCS		2/5			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0000083	PMID:24498631	PCS		2/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001252	PMID:33457206;PMID:24498631	PCS		6/6			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0031964	PMID:33457206	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001943	PMID:33457206;PMID:24498631	PCS		4/6			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0002878	PMID:33457206;PMID:24498631	PCS		4/6			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0008314	PMID:24498631	PCS					P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0003648	PMID:33457206	PCS		2/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001522	PMID:24498631	PCS		2/3			C	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001942	PMID:24498631	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0002039	PMID:24498631	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0003348	PMID:33457206	PCS		2/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0031956	PMID:24498631	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0410288	PMID:33457206;PMID:24498631	PCS		1/5			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0005521	PMID:33457206;PMID:24498631	PCS		4/5			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0011924	PMID:24498631	PCS					P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0002154	PMID:33457206	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0002151	PMID:33457206;PMID:24498631	PCS		6/6			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001639	PMID:33457206	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0000007	PMID:24498631	PCS					I	HPO:probinson[2021-07-08];HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0000846	PMID:33457206	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:619386	Combined oxidative phosphorylation deficiency 52		HP:0001733	PMID:24498631	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0002653	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0002592	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0000280	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0010541	OMIM:161700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0008074	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0006051	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0001805	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0002829	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0009771	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0006175	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0000508	OMIM:161700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0000975	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0001217	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0006465	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0001626	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0000006	OMIM:161700	IEA					I	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0005207	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0001369	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:161700	Necrotizing encephalomyelopathy, subacute, of leigh, adult		HP:0001842	OMIM:161700	IEA					P	HPO:iea[2009-02-17]
OMIM:136880	Fundus albipunctatus		HP:0012045	OMIM:136880	TAS					P	HPO:probinson[2012-09-16]
OMIM:136880	Fundus albipunctatus		HP:0000662	OMIM:136880	TAS					P	HPO:probinson[2009-02-17]
OMIM:136880	Fundus albipunctatus		HP:0030642	OMIM:136880	TAS					P	HPO:skoehler[2017-07-13]
OMIM:136880	Fundus albipunctatus		HP:0000007	OMIM:136880	TAS					I	HPO:skoehler[2017-07-13]
OMIM:136880	Fundus albipunctatus		HP:0000006	OMIM:136880	TAS					I	HPO:probinson[2012-09-16]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002069	PMID:33245860	PCS		4/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002521	PMID:33245860	PCS		3/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002059	PMID:33245860	PCS					P	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0003487	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002376	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0010945	PMID:33245860	PCS	HP:0011461	1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002384	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0001252	PMID:33245860	PCS		2/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0003593	PMID:33245860	PCS		4/7			C	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0010851	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0012736	PMID:33245860	PCS		2/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0011344	PMID:33245860	PCS		5/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0011448	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0001419	PMID:33245860	PCS					I	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0000729	PMID:33245860	PCS		4/7			P	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002509	PMID:33245860	PCS		3/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0000821	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0005949	PMID:33245860	PCS	HP:0003623	5/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0007359	PMID:33245860	PCS		6/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002019	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0001631	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0002027	PMID:33245860	PCS		1/7			P	HPO:probinson[2021-04-27]
OMIM:301058	Developmental and epileptic encephalopathy 90		HP:0003623	PMID:33245860	PCS		3/7			C	HPO:probinson[2021-04-27]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002982	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001374	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001770	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002980	PMID:17264970	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0004322	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000160	PMID:17264970	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0003031	PMID:17264970	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000283	OMIM:304120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0010049	OMIM:304120	TAS					P	HPO:iea[2012-06-03]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000518	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0010055	OMIM:304120	TAS					P	HPO:probinson[2012-06-08]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0011220	OMIM:304120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000316	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0009467	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0003826	OMIM:304120	IEA					C	HPO:skoehler[2010-06-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000238	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0008897	OMIM:304120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002414	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001249	PMID:17264970	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000358	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0003304	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001782	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002751	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000175	PMID:17264970	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000494	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0011800	OMIM:304120	TAS					P	HPO:skoehler[2013-11-28]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0010559	OMIM:304120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0010557	OMIM:304120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0011645	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0006381	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0008087	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0100857	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0010560	OMIM:304120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000926	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000767	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001537	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001539	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000405	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002986	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000047	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0009778	OMIM:304120	IEA					P	HPO:iea[2012-06-08]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000369	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0034391	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000126	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0003577	PMID:17264970	PCS		1/1			C	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001476	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0010109	OMIM:304120	TAS					P	HPO:probinson[2012-06-08]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000260	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0010743	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002878	OMIM:304120	TAS					P	HPO:skoehler[2014-06-24]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000774	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001423	PMID:12612583	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000773	OMIM:304120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002694	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001162	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000272	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000470	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002093	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0005280	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0011304	OMIM:304120	IEA					P	HPO:iea[2012-06-08]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0006160	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001838	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000946	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000349	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0006487	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002007	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0002645	PMID:17264970	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0001631	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000028	OMIM:304120	IEA					P	HPO:iea[2009-02-17]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000347	PMID:17264970	PCS		2/2		HP:0012828	P	HPO:probinson[2012-04-30];HPO:probinson[2022-12-20];HPO:probinson[2022-12-20]
OMIM:304120	Otopalatodigital syndrome, type II		HP:0000501	PMID:17264970	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0005336	OMIM:607812	IEA					P	HPO:iea[2009-02-17]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0003577	PMID:16980979	PCS		4/4			C	HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0001476	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000684	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000343	PMID:16980979	PCS		4/4			P	HPO:probinson[2012-05-01];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000463	OMIM:607812	TAS					P	HPO:skoehler[2013-06-05]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0004322	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0008808	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000260	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0002020	OMIM:607812	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0008070	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0008031	PMID:16980979	PCS		4/4			P	HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000319	PMID:16980979	PCS		4/4			P	HPO:probinson[2012-05-01];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000938	OMIM:607812	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000316	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000219	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000218	PMID:16980979	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000774	PMID:16980979	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000256	OMIM:607812	TAS					P	HPO:skoehler[2013-06-05]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0001763	PMID:16980979	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0005306	OMIM:607812	IEA					P	HPO:iea[2009-02-17]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000336	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0007648	OMIM:607812	IEA					P	HPO:iea[2009-02-17]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000154	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000670	OMIM:607812;PMID:16980979	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000175	OMIM:607812	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0002650	PMID:16980979	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000431	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0002299	PMID:16980979	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0001382	PMID:16980979	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000193	OMIM:607812	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000272	OMIM:607812	IEA					P	HPO:iea[2009-02-17]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0011800	PMID:16980979	PCS		4/4			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0008444	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000426	PMID:16980979	PCS		4/4			P	HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000007	PMID:16980979	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000648	OMIM:607812	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0002208	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0002868	PMID:16980979	PCS		4/4			P	HPO:probinson[2012-05-28];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000565	OMIM:607812	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0002007	PMID:16980979	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000685	OMIM:607812	IEA					P	HPO:iea[2009-02-17]
OMIM:607812	Craniolenticulosutural dysplasia		HP:0000028	PMID:16980979	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:128300	Ear exostoses		HP:0030788	PMID:25459316	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:128300	Ear exostoses		HP:0100777	PMID:25459316	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:128300	Ear exostoses		HP:0000365	PMID:25459316	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:128300	Ear exostoses		HP:0000006	OMIM:128300	IEA					I	HPO:iea[2009-02-17]
OMIM:128300	Ear exostoses		HP:0004459	OMIM:128300	IEA					P	HPO:iea[2009-02-17]
OMIM:128300	Ear exostoses		HP:0410017	PMID:25459316	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0000023	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0001252	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07];HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0002063	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0012707	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0002020	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0003593	PMID:36030551	PCS		1/2			C	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0003270	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0010548	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0012444	PMID:36030551	PCS		2/2			P	HPO:probinson[2023-07-07];HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0001943	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0020221	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0025116	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0001522	PMID:36030551	PCS		2/2			C	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0001348	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0003623	PMID:36030551	PCS		1/2			C	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0000252	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0011968	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0002791	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0002151	PMID:36030551	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0002490	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0100660	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0034671	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0000407	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0001537	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0000007	PMID:36030551	PCS					I	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0000505	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0001511	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0007359	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0003798	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620275	Mitochondrial complex IV deficiency, nuclear type 23		HP:0034391	PMID:36030551	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0004325	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000175	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0001363	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000076	PMID:29432562	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0003577	PMID:29432562	PCS		1/2			C	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0001156	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0004322	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000243	PMID:29432562	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0002197	PMID:29432562	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0003100	PMID:29432562	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0001263	PMID:29432562	PCS		2/2			P	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0005474	PMID:29432562	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0001790	PMID:29432562	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0034197	PMID:29432562	PCS		1/2			C	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0002804	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0001357	PMID:29432562	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000883	PMID:29432562	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000278	PMID:29432562	PCS		2/2			P	HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000006	PMID:29432562	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0001249	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000347	PMID:29432562	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:618265	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development		HP:0000126	PMID:29432562	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001254	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003235	PMID:27448789	PCS		2/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003676	PMID:27448789	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001396	PMID:27448789	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001399	PMID:27448789	PCS		2/2		HP:0003676	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003231	PMID:27448789	PCS		2/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003155	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001394	PMID:27448789	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003073	PMID:27448789	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003270	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0009141	PMID:27448789	PCS		1/1			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001508	PMID:27448789	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001943	PMID:27448789	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003607	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001522	PMID:27448789	PCS		2/2			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0002910	PMID:27448789	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0000952	PMID:27448789	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003623	PMID:27448789	PCS		2/2			C	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001561	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001541	PMID:27448789	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0002098	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0003161	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0002908	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0002904	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001635	PMID:27448789	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0000007	PMID:27448789	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001511	PMID:27448789	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617156	Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)		HP:0001414	PMID:27448789	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-19]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0001561	PMID:25055871	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0030674	PMID:25055871	PCS		3/3			C	HPO:probinson[2022-12-20]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0002803	PMID:25055871	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-20]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0001558	PMID:25055871	PCS		3/3			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-12-20]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0000007	PMID:25055871	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-20]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0002804	PMID:25055871	PCS		3/3			P	HPO:probinson[2022-12-20]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0000256	PMID:25055871	PCS		1/3			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-12-20]
OMIM:616248	Lethal congenital contracture syndrome 6		HP:0010963	PMID:25055871	PCS		3/3			P	HPO:probinson[2022-12-20]
OMIM:605552	Abdominal obesity-metabolic syndrome 1		HP:0000822	OMIM:605552	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605552	Abdominal obesity-metabolic syndrome 1		HP:0012743	OMIM:605552	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605552	Abdominal obesity-metabolic syndrome 1		HP:0000006	OMIM:605552	TAS					I	HPO:skoehler[2017-07-13]
OMIM:142330	Hepatic adenomas, familial		HP:0004904	OMIM:142330	IEA					P	HPO:iea[2009-02-17]
OMIM:142330	Hepatic adenomas, familial		HP:0000147	OMIM:142330	IEA					P	HPO:iea[2009-02-17]
OMIM:142330	Hepatic adenomas, familial		HP:0000006	OMIM:142330	IEA					I	HPO:iea[2009-02-17]
OMIM:142330	Hepatic adenomas, familial		HP:0012028	OMIM:142330	TAS					P	HPO:probinson[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0003577	OMIM:302960	IEA					C	HPO:skoehler[2010-06-19]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000365	PMID:10391218	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0008905	PMID:10391218	PCS		5/8			P	HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0004241	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0012368	OMIM:302960	TAS					P	HPO:skoehler[2013-10-22]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0045075	OMIM:302960	TAS					P	HPO:probinson[2022-05-08]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0008070	OMIM:302960	IEA					P	HPO:skoehler[2010-06-20]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000518	PMID:10391218	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0001508	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000639	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0008131	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002937	PMID:10391218	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0011120	OMIM:302960	TAS					P	HPO:skoehler[2012-10-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0001305	PMID:10391218	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002999	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0008897	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002119	PMID:10391218	PCS		1/8			P	HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002832	PMID:10391218	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000653	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002777	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0001423	PMID:10391218	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000377	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002751	PMID:10391218	PCS		1/8			P	HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000494	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0001561	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002650	PMID:10391218	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002232	PMID:10391218	PCS		7/8			P	HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0003465	OMIM:302960	IEA					P	HPO:skoehler[2010-06-18]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0003462	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000272	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000470	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0010655	PMID:10391218	PCS		5/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0100556	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0100259	PMID:10391218	PCS		1/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000969	OMIM:302960	IEA					P	HPO:skoehler[2010-06-18]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0008420	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0007431	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0001019	PMID:10391218	PCS		6/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000568	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002007	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0007479	PMID:10391218	PCS		1/8			P	HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000765	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000501	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002644	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0001776	PMID:10391218	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0000126	PMID:10391218	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		HP:0002787	OMIM:302960	IEA					P	HPO:iea[2009-02-17]
OMIM:615999	Familial dysalbuminemic hyperthyroxinemia		HP:0033076	PMID:8064810	PCS		0/2			P	HPO:probinson[2021-06-14];HPO:probinson[2021-06-14]
OMIM:615999	Familial dysalbuminemic hyperthyroxinemia		HP:0033077	PMID:29676214	PCS		1/1			P	HPO:probinson[2021-06-14]
OMIM:615999	Familial dysalbuminemic hyperthyroxinemia		HP:0031097	PMID:29676214	PCS		0/1			P	HPO:probinson[2021-06-14]
OMIM:615999	Familial dysalbuminemic hyperthyroxinemia		HP:0000007	PMID:29676214	PCS					I	HPO:probinson[2021-06-14]
OMIM:615999	Familial dysalbuminemic hyperthyroxinemia		HP:0008247	PMID:29676214;PMID:8064810	PCS		3/3			P	HPO:probinson[2021-06-14];HPO:probinson[2021-06-14];HPO:probinson[2021-06-14]
OMIM:615999	Familial dysalbuminemic hyperthyroxinemia		HP:0000006	PMID:8064810	PCS					I	HPO:probinson[2021-06-14];HPO:probinson[2021-06-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0003577	PMID:20004766	PCS		3/3			C	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0001371	OMIM:613330	TAS					P	HPO:skoehler[2015-08-16]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0004288	PMID:20004766	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0001270	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0100255	PMID:20004766	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0031096	PMID:20004766	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000316	OMIM:613330	TAS					P	HPO:skoehler[2015-08-16]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000238	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0002812	PMID:20004766	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0001847	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0009623	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0002857	OMIM:613330	TAS					P	HPO:skoehler[2015-08-16]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000256	OMIM:613330	TAS					P	HPO:skoehler[2015-08-16]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000773	OMIM:613330	TAS					P	HPO:probinson[2013-06-02]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0003521	PMID:20004766	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0002751	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000252	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0002650	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0001762	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0001288	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0002970	OMIM:613330	TAS					P	HPO:probinson[2013-06-02]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0003025	PMID:20004766	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000470	PMID:20004766	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0010580	OMIM:613330	TAS					P	HPO:skoehler[2015-08-16]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000946	OMIM:613330	TAS					P	HPO:skoehler[2015-08-16]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0001518	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0002827	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000007	PMID:20004766	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0003418	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0000768	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0001538	OMIM:613330	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0003316	PMID:20004766	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0008788	PMID:20004766	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0005659	PMID:20004766	PCS		1/3			P	HPO:probinson[2022-12-14]
OMIM:613330	Spondylo-megaepiphyseal-metaphyseal dysplasia		HP:0002866	PMID:20004766	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:613456	Frontonasal dysplasia 3		HP:0002223	OMIM:613456	TAS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000175	OMIM:613456	TAS					P	HPO:probinson[2013-06-02]
OMIM:613456	Frontonasal dysplasia 3		HP:0000431	OMIM:613456	TAS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0002057	OMIM:613456	TAS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000430	OMIM:613456	TAS					P	HPO:probinson[2013-06-02]
OMIM:613456	Frontonasal dysplasia 3		HP:0000316	OMIM:613456	TAS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000007	PMID:20451171	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000568	OMIM:613456	TAS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000636	OMIM:613456	TAS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000653	OMIM:613456	TAS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000248	OMIM:613456	TAS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0001249	OMIM:613456	TAS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000369	PMID:20451171	PCS		3/3			P	HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0000358	PMID:20451171	PCS		3/3			P	HPO:probinson[2023-02-20]
OMIM:613456	Frontonasal dysplasia 3		HP:0002006	OMIM:613456	TAS					P	HPO:probinson[2013-06-02]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001397	PMID:27876313	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0003233	PMID:8254026	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001399	PMID:31230978	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001971	PMID:31230978	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001395	PMID:27876313	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0002240	PMID:31230978;PMID:27876313;PMID:8254026	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-30];HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001394	PMID:31230978;PMID:27876313	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0003593	PMID:21963785;PMID:31230978;PMID:27876313	PCS		4/6			C	HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0002040	PMID:31230978	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0031205	PMID:21963785;PMID:31230978;PMID:27876313;PMID:8254026	PCS		7/7			P	HPO:probinson[2021-06-30];HPO:probinson[2021-06-30];HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0031964	PMID:31230978;PMID:27876313	PCS		5/5			P	HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001409	PMID:31230978	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001508	PMID:21963785	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001903	PMID:31230978	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001405	PMID:27876313	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0025435	PMID:27876313	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0006554	PMID:21963785	PCS		1/1			P	HPO:probinson[2021-06-30];HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001522	OMIM:278000	IEA					C	HPO:iea[2009-02-17]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001744	PMID:31230978;PMID:8254026	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-30];HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0002014	PMID:27876313	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0031956	PMID:31230978;PMID:27876313	PCS		4/5			P	HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0003621	PMID:27876313	PCS		2/4			C	HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0002155	PMID:31230978;PMID:27876313;PMID:8254026	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-30];HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0003124	PMID:31230978;PMID:27876313;PMID:8254026	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-30];HPO:probinson[2021-06-30];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001882	PMID:31230978	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0002013	PMID:27876313	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0005521	PMID:21963785	PCS		1/1			P	HPO:probinson[2021-06-30];HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0004333	OMIM:278000	IEA					P	HPO:iea[2009-02-17]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0003141	PMID:8254026	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0002570	OMIM:278000	IEA					P	HPO:iea[2009-02-17]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0003282	PMID:27876313	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0030948	PMID:27876313	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0034029	PMID:27876313	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0012852	PMID:27876313	PCS		1/4			P	HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0010512	PMID:21963785;PMID:27876313;PMID:8254026	PCS		2/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-06-30];HPO:probinson[2021-09-24];HPO:probinson[2021-06-30];HPO:probinson[2024-03-09]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0031141	PMID:31230978	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0000007	PMID:21963785	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0000846	PMID:21963785	PCS		1/1			P	HPO:probinson[2021-06-30];HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001538	PMID:27876313	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-24]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001873	PMID:31230978	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:278000	Lysosomal acid lipase deficiency		HP:0001433	PMID:21963785	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-30]
OMIM:608710	Granulomatosis with polyangiitis		HP:0002102	PMID:26684637	IEA					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0032979	PMID:28410589	PCS					P	HPO:probinson[2020-07-08];HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0003596	PMID:26684637	PCS					C	HPO:probinson[2020-08-26];HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0025420	PMID:25149391	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0010982	PMID:22808956	PCS					I	HPO:probinson[2020-06-14]
OMIM:608710	Granulomatosis with polyangiitis		HP:0032018	PMID:25149391	PCS					P	HPO:probinson[2020-07-08];HPO:probinson[2023-07-18]
OMIM:608710	Granulomatosis with polyangiitis		HP:0032977	PMID:21885400	PCS					P	HPO:probinson[2020-06-14]
OMIM:608710	Granulomatosis with polyangiitis		HP:0001607	PMID:31199488;PMID:26684637	PCS		105/972	FEMALE		P	HPO:probinson[2020-07-08];HPO:probinson[2020-08-26];HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0011120	PMID:25149391	IEA					P	HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0002955	PMID:22808956	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-06-14]
OMIM:608710	Granulomatosis with polyangiitis		HP:0001945	PMID:25149391	PCS					P	HPO:probinson[2020-07-08];HPO:probinson[2023-07-18]
OMIM:608710	Granulomatosis with polyangiitis		HP:0001824	PMID:25149391	PCS					P	HPO:probinson[2020-07-08];HPO:probinson[2023-07-18]
OMIM:608710	Granulomatosis with polyangiitis		HP:0000554	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0002777	PMID:25630847	PCS		6/35			P	HPO:probinson[2020-07-08];HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0200042	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0003326	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0002113	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0031417	PMID:25149391	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0000155	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0000573	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0000491	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0012735	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0410280	PMID:19877069	PCS					C	HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0034920	PMID:2001873	PCS		7/17			P	HPO:probinson[2023-07-18]
OMIM:608710	Granulomatosis with polyangiitis		HP:0002093	PMID:25149391	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0012378	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0032229	PMID:27428559	PCS		33/321			P	HPO:probinson[2020-07-08];HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0100534	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0100758	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0032230	PMID:27428559;PMID:22808956	PCS		283/331			P	HP:probinson[2019-04-19];HPO:probinson[2020-06-14];HPO:probinson[2020-07-08];HPO:probinson[2020-08-26]
OMIM:608710	Granulomatosis with polyangiitis		HP:0032990	PMID:25149391	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0000509	PMID:26684637	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0000246	PMID:25149391	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0000389	PMID:25149391	PCS					P	HPO:probinson[2020-07-08]
OMIM:608710	Granulomatosis with polyangiitis		HP:0025406	PMID:25149391	PCS					P	HPO:probinson[2020-07-08];HPO:probinson[2023-07-18]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0003774	PMID:31481669	PCS	HP:0003593	3/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0001166	PMID:31481669	PCS		2/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0003577	PMID:31481669	PCS		1/3			C	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0000252	PMID:31481669	PCS		3/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0002059	PMID:31481669	PCS		1/2			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0002188	PMID:31481669	PCS		2/2			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0001272	PMID:31481669	PCS		1/2			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0001252	PMID:31481669	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0003593	PMID:31481669	PCS		2/3			C	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0005484	PMID:31481669	PCS		2/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0031266	PMID:31481669	PCS		1/2			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0000093	PMID:31481669	PCS		3/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0011451	PMID:31481669	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0000007	PMID:31481669	PCS					I	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0001967	PMID:31481669	PCS		2/2			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0000851	PMID:31481669	PCS	HP:0003577	3/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0001336	PMID:31481669	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:619609	Galloway-Mowat syndrome 10		HP:0009879	PMID:31481669	PCS		1/2			P	HPO:probinson[2022-02-01]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001254	PMID:3812589	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0004322	PMID:9683607	PCS		3/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001250	PMID:9683607	PCS		2/4			P	HPO:probinson[2024-03-09];HPO:skoehler[2013-10-06]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001252	PMID:9683607;PMID:3812589	PCS		3/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0003593	PMID:9683607;PMID:3812589	PCS		2/4			C	HPO:probinson[2024-03-09];HPO:skoehler[2013-10-06]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002160	PMID:9683607	PCS		3/3			P	HPO:skoehler[2013-10-06]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0000639	OMIM:250940;PMID:9683607	PCS		5/13			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09];HPO:skoehler[2013-10-06]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001508	PMID:9683607	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0000618	OMIM:250940	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001889	PMID:9683607;PMID:3812589	PCS		4/4			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09];HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002878	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001763	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0000952	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001249	OMIM:250940	IEA					P	HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0003623	PMID:9683607;PMID:9453374	PCS		3/4			C	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0003524	PMID:9453374;PMID:3812589	PCS		2/2			P	HPO:probinson[2024-03-09];HPO:skoehler[2015-01-21]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002311	OMIM:250940	IEA					P	HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002014	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001583	PMID:9683607	PCS		2/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0000252	PMID:9683607	PCS		2/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002059	OMIM:250940	IEA					P	HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002013	PMID:3812589	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002156	PMID:9683607;PMID:9453374;PMID:3812589	PCS		3/3			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09];HPO:probinson[2024-03-09];HPO:skoehler[2013-10-06]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001288	OMIM:250940	TAS					P	HPO:skoehler[2013-10-06]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0003223	OMIM:250940	IEA					P	HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002098	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0002197	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0011968	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001263	PMID:9683607	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0011344	PMID:9683607	PCS		2/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0040126	PMID:3812589	PCS		0/1			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0040087	PMID:3812589	PCS		0/1			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0012120	PMID:9683607;PMID:3812589	PCS		0/4			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09];HPO:skoehler[2013-05-30];HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0000007	PMID:12068375	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001257	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0003658	PMID:9683607;PMID:9453374;PMID:3812589	PCS		5/5			P	HPO:probinson[2024-03-09];HPO:iea[2009-02-17]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001510	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001238	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:250940	Homocystinuria-megaloblastic anemia, cblG complementation type		HP:0001875	PMID:9683607	PCS		1/3			P	HPO:probinson[2024-03-09]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0003676	OMIM:615033	TAS					C	HPO:skoehler[2013-06-05]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0000486	PMID:23176823	PCS		9/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0004322	OMIM:615033	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0003396	PMID:23176823	PCS		2/4			P	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0000020	PMID:23176823	PCS		4/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0002063	PMID:23176823	PCS		2/12			P	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0030891	PMID:23176823	PCS		11/11			P	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0007340	OMIM:615033	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0011463	PMID:23176823	PCS					C	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0000338	PMID:23176823	PCS		3/12			P	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0000218	OMIM:615033	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0002019	PMID:23176823	PCS		7/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0001249	OMIM:615033	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0001347	PMID:23176823	PCS		12/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0002015	PMID:23176823	PCS		6/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0003487	OMIM:615033	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0002079	PMID:23176823	PCS		11/11			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0008959	PMID:23176823	PCS		3/12			P	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0001761	PMID:23176823	PCS		2/12			P	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0001260	PMID:23176823	PCS		9/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0001263	PMID:23176823	PCS		12/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0000609	PMID:23176823	PCS		3/5			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0009053	PMID:23176823	PCS		9/12			P	HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0000506	OMIM:615033	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0002607	PMID:23176823	PCS		3/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0000007	PMID:23176823	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0001258	PMID:23176823	PCS		12/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:615033	Spastic paraplegia 54, autosomal recessive		HP:0006986	PMID:23176823	PCS		5/12			P	HPO:probinson[2022-11-06]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0003048	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0000430	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0005880	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0010049	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0009843	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0008368	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0009702	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0000006	OMIM:186400	IEA					I	HPO:iea[2009-02-17]
OMIM:186400	Synostoses, tarsal, carpal, and digital		HP:0001798	OMIM:186400	IEA					P	HPO:iea[2009-02-17]
OMIM:144755	Hyperostosis cranialis interna		HP:0009926	OMIM:144755	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:144755	Hyperostosis cranialis interna		HP:0010628	PMID:20140965	PCS		9/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0003621	PMID:20140965	PCS					C	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0001751	PMID:20140965	PCS		10/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0000265	OMIM:144755	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:144755	Hyperostosis cranialis interna		HP:0007906	PMID:20140965	PCS		1/13			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0000360	PMID:20140965	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0005890	PMID:20140965	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0004490	PMID:20140965	PCS		13/13			P	HPO:probinson[2014-04-22];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0000407	PMID:20140965	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0007099	PMID:20140965	PCS		1/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0011462	PMID:20140965	PCS					C	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0200026	OMIM:144755	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:144755	Hyperostosis cranialis interna		HP:0004409	OMIM:144755	IEA					P	HPO:skoehler[2019-09-07]
OMIM:144755	Hyperostosis cranialis interna		HP:0007663	OMIM:144755	IEA					P	HPO:skoehler[2018-10-08]
OMIM:144755	Hyperostosis cranialis interna		HP:0000458	PMID:20140965	PCS	HP:0011462	6/13			P	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0000648	OMIM:144755	IEA					P	HPO:skoehler[2018-10-08]
OMIM:144755	Hyperostosis cranialis interna		HP:0002315	PMID:20140965	PCS	HP:0011462	5/10			P	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0000520	OMIM:144755	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:144755	Hyperostosis cranialis interna		HP:0000006	PMID:29621230	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:144755	Hyperostosis cranialis interna		HP:0005746	PMID:20140965	PCS		13/13			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-01]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0005359	PMID:28823388	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0003212	OMIM:102700	TAS					P	HPO:probinson[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001890	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002240	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0003593	PMID:28823388	IEA		1/1			C	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001270	PMID:28823388	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001508	PMID:16724639;PMID:28823388	PCS		2/2			P	HPO:probinson[2022-05-14];HPO:probinson[2009-02-17];HPO:probinson[2022-03-31]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0011123	PMID:28823388	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002718	OMIM:102700	TAS					P	HPO:probinson[2012-04-26]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0012191	OMIM:102700	TAS					P	HPO:probinson[2010-06-20]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001888	PMID:16724639;PMID:28823388	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31];HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001967	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0006532	PMID:16724639;PMID:28823388	PCS		2/2			P	HPO:probinson[2022-05-14];HPO:probinson[2022-03-31]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001744	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0003623	PMID:28823388	PCS		1/1			C	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002850	OMIM:102700	TAS					P	HPO:probinson[2015-02-15]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002014	PMID:16724639	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0005424	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001880	PMID:28823388	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0034829	PMID:4014441	PCS		6/8			P	HPO:probinson[2023-07-18]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001442	OMIM:102700	IEA					I	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002099	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0004430	PMID:16724639;PMID:28823388	PCS		2/2			P	HPO:probinson[2022-05-14];HPO:probinson[2012-04-26];HPO:probinson[2022-03-31]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0031233	PMID:28823388	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002090	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0010976	OMIM:102700	TAS		20/20		HP:0012828	P	HPO:probinson[2009-02-17];HPO:skoehler[2012-10-09]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0000907	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0031164	OMIM:102700	IEA					P	HPO:skoehler[2019-09-07]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002728	PMID:28823388	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0000926	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001954	PMID:28823388	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0030273	PMID:28823388	PCS		1/1			P	HPO:probinson[2015-02-15];HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0000007	PMID:3007108	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-31];HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0004429	OMIM:102700	TAS					P	HPO:probinson[2012-04-26]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0000988	PMID:28823388	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0001973	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0000246	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0008348	OMIM:102700	TAS					P	HPO:probinson[2015-02-15]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002720	OMIM:102700	TAS					P	HPO:probinson[2015-02-15]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002841	OMIM:102700	TAS					P	HPO:probinson[2012-04-26]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002644	OMIM:102700	IEA					P	HPO:iea[2009-02-17]
OMIM:102700	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency		HP:0002028	PMID:16724639;PMID:28823388	PCS		2/2			P	HPO:probinson[2022-05-14];HPO:probinson[2022-03-31]
OMIM:617142	Aniridia 3		HP:0003577	PMID:26394807	PCS		8/8			C	HPO:probinson[2023-05-19]
OMIM:617142	Aniridia 3		HP:0000518	PMID:26394807	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-19]
OMIM:617142	Aniridia 3		HP:0000639	PMID:26394807	PCS		0/8			P	HPO:probinson[2023-05-19]
OMIM:617142	Aniridia 3		HP:0007663	PMID:26394807	PCS		8/8			P	HPO:probinson[2023-05-19]
OMIM:617142	Aniridia 3		HP:0000526	PMID:26394807	PCS	HP:0003577	8/8			P	HPO:probinson[2023-05-19]
OMIM:617142	Aniridia 3		HP:0000501	PMID:26394807	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-19]
OMIM:617142	Aniridia 3		HP:0000006	PMID:26394807	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-19]
OMIM:601708	Superior transverse scapular ligament, calcification of, familial		HP:0011989	OMIM:601708	TAS					P	HPO:probinson[2012-07-25]
OMIM:601708	Superior transverse scapular ligament, calcification of, familial		HP:0000006	OMIM:601708	TAS					I	HPO:skoehler[2009-02-17]
OMIM:601708	Superior transverse scapular ligament, calcification of, familial		HP:0012216	OMIM:601708	TAS					P	HPO:probinson[2013-03-14]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001276	PMID:30715177	PCS		1/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0003577	PMID:30715177	PCS		7/7			C	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000343	PMID:25330800	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0004840	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001250	PMID:30715177	PCS		7/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000083	PMID:30715177	PCS		2/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000160	PMID:25330800	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001252	PMID:25330800;PMID:30715177	PCS		6/8			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0012595	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000639	PMID:30715177	PCS		6/6			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001508	PMID:25330800	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001903	PMID:30715177	PCS		3/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0008972	PMID:25330800	IEA		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001946	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002514	PMID:30715177;PMID:21427441	PCS		8/8			P	HPO:probinson[2021-05-30];HPO:probinson[2023-08-22];HPO:probinson[2023-08-22]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0003348	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002510	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000252	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001344	PMID:30715177	PCS		6/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0003542	PMID:30715177	PCS		2/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002376	PMID:30715177	PCS		5/5		HP:0025215	P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0031936	PMID:30715177	PCS		7/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002013	PMID:25330800	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002750	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002352	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002151	PMID:25330800;PMID:30715177	PCS		4/8			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001263	PMID:25330800;PMID:21427441	PCS		2/2			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0010818	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0011344	PMID:30715177	PCS		7/7			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0003819	PMID:30715177	PCS		2/7			C	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001518	PMID:25330800	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000407	PMID:25330800;PMID:21427441	PCS		2/2			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000821	PMID:25330800	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0040209	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0000007	PMID:21427441	PCS					I	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0002304	PMID:21427441	PCS		1/1			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0001510	PMID:25330800	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619147	Leukoencephalopathy, progressive, infantile-onset, with or without deafness		HP:0008527	PMID:30715177	PCS	HP:0003577	7/7			P	HPO:probinson[2021-05-30]
OMIM:107650	Apnea, obstructive sleep		HP:0002870	OMIM:107650	TAS					P	HPO:probinson[2009-02-17]
OMIM:107650	Apnea, obstructive sleep		HP:0002384	OMIM:107650	TAS					P	HPO:probinson[2009-02-17]
OMIM:107650	Apnea, obstructive sleep		HP:0025267	OMIM:107650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:107650	Apnea, obstructive sleep		HP:0001262	OMIM:107650	TAS					P	HPO:skoehler[2010-06-20]
OMIM:107650	Apnea, obstructive sleep		HP:0000458	OMIM:107650	TAS					P	HPO:probinson[2009-02-17]
OMIM:107650	Apnea, obstructive sleep		HP:0000006	OMIM:107650	TAS					I	HPO:probinson[2009-02-17]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0009161	OMIM:609432	TAS					P	HPO:probinson[2012-07-16]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0003577	PMID:25466284	PCS					C	HPO:probinson[2024-07-22]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0009177	OMIM:609432	IEA					P	HPO:iea[2009-02-17]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0008362	OMIM:609432	IEA					P	HPO:iea[2009-02-17]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0006097	PMID:25466284	PCS					P	HPO:probinson[2012-07-16];HPO:probinson[2024-07-22]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0010064	OMIM:609432	TAS					P	HPO:probinson[2009-02-17]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0000954	OMIM:609432	TAS				HP:0012832	P	HPO:probinson[2009-02-17]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0000007	PMID:25466284	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-07-22]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0009601	OMIM:609432	TAS					P	HPO:probinson[2009-02-17]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0009568	OMIM:609432	TAS					P	HPO:probinson[2012-07-16]
OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		HP:0004209	OMIM:609432	TAS					P	HPO:probinson[2009-02-17]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0001276	PMID:34415322	PCS		2/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0008969	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0003273	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0003593	PMID:34415322	PCS		1/2			C	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0100543	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0000639	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0007340	PMID:34415322	PCS		2/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0100702	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0002359	PMID:34415322	PCS		2/2			P	HPO:probinson[2022-01-31];HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0001347	PMID:34415322	PCS		2/2			P	HPO:probinson[2022-01-31];HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0003621	PMID:34415322	PCS		1/2			C	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0003487	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0001288	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0001761	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0000012	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0100280	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0002495	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0010873	PMID:34415322	PCS		2/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0031993	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0011448	PMID:34415322	PCS		2/2			P	HPO:probinson[2022-01-31];HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0006380	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0000007	PMID:34415322	PCS					I	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0006466	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0030051	PMID:34415322	PCS		1/2			P	HPO:probinson[2022-01-31]
OMIM:619621	Spastic paraplegia 84, autosomal recessive		HP:0001258	PMID:34415322	PCS		2/2			P	HPO:probinson[2022-01-31];HPO:probinson[2022-01-31]
OMIM:610163	Immunodeficiency 25		HP:0005403	PMID:16672702	PCS		1/1			P	HPO:probinson[2013-03-12];HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0001880	PMID:16672702	PCS	HP:0003593	1/1			P	HPO:probinson[2013-03-12];HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0005401	PMID:16672702	PCS		1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0003212	PMID:16672702	PCS		1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0003496	PMID:16672702	PCS		1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0030167	PMID:1635567	PCS		1/2			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0004385	PMID:16672702	PCS	HP:0003593	1/1			P	HPO:probinson[2013-03-12];HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0005353	PMID:16672702	PCS	HP:0011463	1/1			P	HPO:probinson[2013-03-12];HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0410295	PMID:16672702	PCS		1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0003262	PMID:1635567	PCS		1/2			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0001890	PMID:1635567	PCS		1/2			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0003593	PMID:16672702	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0003261	PMID:16672702	PCS		1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0000007	PMID:16672702	PCS					I	HPO:probinson[2013-01-09]
OMIM:610163	Immunodeficiency 25		HP:0001019	PMID:16672702	PCS	HP:0003593	1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0006532	PMID:16672702	PCS		1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0008348	PMID:1635567	PCS		2/2			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0003237	PMID:16672702	PCS		1/1			P	HPO:probinson[2020-11-03]
OMIM:610163	Immunodeficiency 25		HP:0002721	PMID:16672702	PCS					P	HPO:probinson[2013-03-12]
OMIM:604116	Cone-rod dystrophy 3		HP:0000572	PMID:12037008	PCS					P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0003621	PMID:12037008	PCS		10/12			C	HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0000551	PMID:12037008	PCS		10/10			P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0000580	PMID:12796258	PCS					P	HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0011504	PMID:12037008	PCS		4/12			P	HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0011463	PMID:12037008	PCS		1/12			C	HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0011462	PMID:12037008	PCS		1/12			C	HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0000007	PMID:12796258	PCS					I	HPO:nvasilevsky[2019-03-11];HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0007994	PMID:12796258	PCS		10/16			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0000548	PMID:12796258	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0000603	PMID:12796258;PMID:12037008	PCS		17/28			P	HPO:probinson[2020-07-20];HPO:skoehler[2013-01-10];HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0007984	PMID:12796258	PCS					P	HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0000543	PMID:12796258	PCS					P	HPO:probinson[2020-07-20]
OMIM:604116	Cone-rod dystrophy 3		HP:0007843	PMID:12796258	PCS					P	HPO:probinson[2020-07-20]
OMIM:614305	Sclerosteosis 2		HP:0010628	PMID:21471202	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0000365	PMID:21471202	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0002321	PMID:21471202	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0002684	PMID:21471202	PCS		2/2			P	HPO:probinson[2023-02-21];HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0002497	PMID:21471202	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0001288	PMID:21471202	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0002164	PMID:21471202	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0001293	PMID:21471202	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0002273	OMIM:614305	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614305	Sclerosteosis 2		HP:0010554	PMID:21471202	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0009381	OMIM:614305	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614305	Sclerosteosis 2		HP:0000316	OMIM:614305	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614305	Sclerosteosis 2		HP:0000007	PMID:21471202	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0002007	OMIM:614305	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614305	Sclerosteosis 2		HP:0000256	OMIM:614305	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614305	Sclerosteosis 2		HP:0000303	OMIM:614305	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614305	Sclerosteosis 2		HP:0000006	PMID:21471202	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614305	Sclerosteosis 2		HP:0000324	PMID:21471202	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:187050	Teeth present at birth		HP:0000695	OMIM:187050	IEA					P	HPO:iea[2009-02-17]
OMIM:187050	Teeth present at birth		HP:0000006	OMIM:187050	IEA					I	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0004322	OMIM:270460	IEA					P	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0001629	OMIM:270460	IEA					P	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0000160	OMIM:270460	IEA					P	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0001042	OMIM:270460	IEA					P	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0000007	OMIM:270460	IEA					I	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0000311	OMIM:270460	IEA					P	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0005280	OMIM:270460	IEA					P	HPO:iea[2009-02-17]
OMIM:270460	Sonoda syndrome		HP:0001249	OMIM:270460	IEA					P	HPO:iea[2009-02-17]
OMIM:616260	Tenorio syndrome		HP:0002003	PMID:25196541	PCS		2/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0002389	PMID:25196541	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000463	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0002120	PMID:25196541	PCS		2/4			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001250	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001252	PMID:25196541	PCS		4/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0002020	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001097	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001270	PMID:25196541	PCS		1/6			P	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000938	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000739	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000712	PMID:25196541	PCS		1/6			P	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000998	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000238	PMID:25196541	PCS		1/4		HP:0012825	P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001943	PMID:25196541	PCS		3/4			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001528	PMID:25196541	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0002119	PMID:25196541	PCS		2/4			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0006532	PMID:25196541	PCS		1/6			P	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000158	PMID:25196541	PCS		2/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0040216	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000256	PMID:25196541	PCS		6/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001249	PMID:25196541	PCS		5/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0003623	PMID:25196541	PCS		5/5			C	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000154	PMID:25196541	PCS		1/6			P	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0002312	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000750	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0002650	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000574	OMIM:616260	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616260	Tenorio syndrome		HP:0001288	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001382	PMID:25196541	PCS		1/6			P	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000270	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001263	PMID:25196541	PCS					P	HPO:skoehler[2019-02-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0030880	PMID:25196541	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0100021	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0011107	PMID:25196541	PCS		1/6			P	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000506	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000805	PMID:25196541	PCS		1/6			P	HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0001279	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0002104	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000006	PMID:25196541	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000303	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:616260	Tenorio syndrome		HP:0000445	PMID:25196541	PCS		1/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-01-16]
OMIM:307830	Hypouricemia, familial renal, due to tubular hypersecretion		HP:0001419	OMIM:307830	TAS					I	HPO:probinson[2009-02-17]
OMIM:307830	Hypouricemia, familial renal, due to tubular hypersecretion		HP:0003537	OMIM:307830	TAS					P	HPO:probinson[2009-02-17]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0003477	PMID:23176821	PCS		1/3			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-07-10]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0003621	PMID:23176821	PCS		2/3			C	HPO:iea[2009-02-17];HPO:probinson[2022-03-03]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0002650	OMIM:609340	IEA					P	HPO:iea[2009-02-17]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0001761	OMIM:609340	IEA					P	HPO:iea[2009-02-17]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0001288	PMID:23176821	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-03]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0003487	OMIM:609340	IEA					P	HPO:iea[2009-02-17]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0003593	PMID:23176821	PCS		1/3			C	HPO:probinson[2022-03-03]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0002061	PMID:23176821	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-03]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0007340	OMIM:609340	IEA					P	HPO:iea[2009-02-17]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0000007	PMID:23176821	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-03]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0002936	OMIM:609340	IEA					P	HPO:iea[2009-02-17]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0001258	PMID:23176821	PCS		1/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-03]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0003677	OMIM:609340	IEA					C	HPO:iea[2009-02-17]
OMIM:609340	Spastic paraplegia 28, autosomal recessive		HP:0001347	PMID:23176821	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-03]
OMIM:259780	Otoonychoperoneal syndrome		HP:0001597	OMIM:259780	IEA					P	HPO:iea[2009-02-17]
OMIM:259780	Otoonychoperoneal syndrome		HP:0003273	OMIM:259780	TAS					P	HPO:probinson[2012-07-16]
OMIM:259780	Otoonychoperoneal syndrome		HP:0011247	OMIM:259780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259780	Otoonychoperoneal syndrome		HP:0001270	OMIM:259780	IEA					P	HPO:iea[2009-02-17]
OMIM:259780	Otoonychoperoneal syndrome		HP:0006380	OMIM:259780	TAS					P	HPO:probinson[2012-07-16]
OMIM:259780	Otoonychoperoneal syndrome		HP:0006492	OMIM:259780	TAS					P	HPO:probinson[2010-06-18]
OMIM:259780	Otoonychoperoneal syndrome		HP:0000007	OMIM:259780	IEA					I	HPO:iea[2009-02-17]
OMIM:259780	Otoonychoperoneal syndrome		HP:0006466	OMIM:259780	TAS					P	HPO:probinson[2012-07-16]
OMIM:259780	Otoonychoperoneal syndrome		HP:0006587	OMIM:259780	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:259780	Otoonychoperoneal syndrome		HP:0000598	OMIM:259780	IEA					P	HPO:iea[2009-02-17]
OMIM:259780	Otoonychoperoneal syndrome		HP:0000400	OMIM:259780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259780	Otoonychoperoneal syndrome		HP:0000268	OMIM:259780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259780	Otoonychoperoneal syndrome		HP:0000047	OMIM:259780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259780	Otoonychoperoneal syndrome		HP:0000369	OMIM:259780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259780	Otoonychoperoneal syndrome		HP:0000358	OMIM:259780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:550500	Myoglobinuria, recurrent		HP:0003200	OMIM:550500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:550500	Myoglobinuria, recurrent		HP:0003652	OMIM:550500	TAS					P	HPO:skoehler[2015-01-21]
OMIM:550500	Myoglobinuria, recurrent		HP:0001427	OMIM:550500	TAS					I	HPO:skoehler[2009-02-17]
OMIM:550500	Myoglobinuria, recurrent		HP:0008305	OMIM:550500	TAS					P	HPO:probinson[2013-03-30]
OMIM:276950	Vacterl association with hydrocephalus		HP:0002410	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0002023	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0000089	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0002093	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0000925	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0003826	OMIM:276950	TAS					C	HPO:probinson[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0000238	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0030680	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0000007	OMIM:276950	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:276950	Vacterl association with hydrocephalus		HP:0009777	OMIM:276950	IEA					P	HPO:iea[2009-02-17]
OMIM:276950	Vacterl association with hydrocephalus		HP:0002878	OMIM:276950	TAS					P	HPO:skoehler[2014-06-24]
OMIM:276950	Vacterl association with hydrocephalus		HP:0001627	OMIM:276950	TAS					P	HPO:skoehler[2015-12-30]
OMIM:276950	Vacterl association with hydrocephalus		HP:0006433	OMIM:276950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:276950	Vacterl association with hydrocephalus		HP:0003468	OMIM:276950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619806	Spinocerebellar ataxia 49		HP:0003621	PMID:35310830	PCS		2/9			C	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0003596	PMID:35310830	PCS		6/9			C	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0000640	PMID:35310830	PCS	HP:0003596	9/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0000651	PMID:35310830	PCS		4/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0000486	PMID:35310830	PCS		2/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0003487	PMID:35310830	PCS		2/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0001310	PMID:35310830	PCS		7/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0001761	PMID:35310830	PCS		1/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0001272	PMID:35310830	PCS		5/5			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0001260	PMID:35310830	PCS		5/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0001251	PMID:35310830	PCS		7/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0002075	PMID:35310830	PCS		1/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0003390	PMID:35310830	PCS		5/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0002071	PMID:35310830	PCS		0/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0000726	PMID:35310830	PCS		0/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0002317	PMID:35310830	PCS					P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0025710	PMID:35310830	PCS		1/9			C	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0002505	PMID:35310830	PCS	HP:0003584	2/9			P	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0000006	PMID:35310830	PCS					I	HPO:probinson[2022-06-14]
OMIM:619806	Spinocerebellar ataxia 49		HP:0001347	PMID:35310830	PCS		9/9			P	HPO:probinson[2022-06-14]
OMIM:169610	Pemphigus vulgaris, familial		HP:0002960	OMIM:169610	TAS					P	HPO:probinson[2009-02-17]
OMIM:169610	Pemphigus vulgaris, familial		HP:0030057	OMIM:169610	TAS					P	HPO:probinson[2009-02-17]
OMIM:169610	Pemphigus vulgaris, familial		HP:0008066	OMIM:169610	TAS					P	HPO:skoehler[2013-06-05]
OMIM:169610	Pemphigus vulgaris, familial		HP:0000006	OMIM:169610	TAS					I	HPO:skoehler[2013-05-29]
OMIM:169610	Pemphigus vulgaris, familial		HP:0200097	OMIM:169610	TAS					P	HPO:probinson[2015-06-04]
OMIM:205000	Amyotonia congenita		HP:0003202	OMIM:205000	IEA					P	HPO:iea[2009-02-17]
OMIM:205000	Amyotonia congenita		HP:0000007	OMIM:205000	IEA					I	HPO:iea[2009-02-17]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0011463	PMID:20038800	PCS		1/1			C	HPO:probinson[2021-05-09]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0005387	PMID:20038800	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0003493	PMID:20038800	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0002718	OMIM:613495	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0011839	PMID:20038800	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0032134	PMID:20038800	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0000007	PMID:20038800	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0002205	PMID:20038800	PCS	HP:0011463	1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:613495	Immunodeficiency, common variable, 5		HP:0010975	PMID:20038800	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002322	PMID:18570303	PCS		1/2			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0003236	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002067	PMID:18570303	PCS		3/3			P	HPO:probinson[2013-04-07];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001332	PMID:18570303	PCS		3/3			P	HPO:probinson[2013-04-07];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002145	OMIM:612953	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002283	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002063	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0025387	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000716	PMID:18570303	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000639	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000718	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0011462	PMID:18570303	PCS		2/3			C	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0006892	OMIM:612953	TAS					P	HPO:probinson[2013-04-07]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000338	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000658	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001269	PMID:18570303	PCS		1/2			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001268	PMID:18570303	PCS		2/2			P	HPO:probinson[2013-04-07];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000751	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001348	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000017	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001347	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000511	PMID:18570303	PCS		1/2			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002312	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002378	PMID:18570303	PCS		1/2			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0003621	PMID:18570303	PCS		1/3			C	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001300	PMID:18570303	PCS		3/3			P	HPO:probinson[2013-04-07];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002530	PMID:18570303	PCS		1/2			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0025097	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001260	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0011468	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002172	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0011448	PMID:18570303	PCS		2/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0100660	PMID:18570303	PCS		2/2			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0031833	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0007351	PMID:18570303	PCS		1/2			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0000007	PMID:18570303	PCS					I	HPO:probinson[2013-04-07];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0002505	PMID:18570303	PCS		1/3			P	HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001257	PMID:18570303	PCS		1/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0001337	PMID:18570303	PCS		2/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:612953	Parkinson disease 14, autosomal recessive		HP:0003678	PMID:18570303	PCS					C	HPO:skoehler[2013-05-03];HPO:probinson[2022-06-26]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0031834	PMID:20413652	PCS		1/5			P	HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001674	OMIM:208530	IEA					P	HPO:iea[2009-02-17]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001696	PMID:20413652	PCS		2/5			P	HPO:skoehler[2013-09-30];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0002101	OMIM:208530	TAS					P	HPO:probinson[2013-04-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001651	PMID:20413652	PCS		2/5			P	HPO:skoehler[2013-09-30];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001750	PMID:20413652	PCS					P	HPO:skoehler[2018-10-08];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0000023	PMID:28991257	PCS		2/10			P	HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001274	OMIM:208530	IEA					P	HPO:iea[2009-02-17]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0011565	PMID:20413652	PCS		5/5			P	HPO:skoehler[2013-09-30];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0031565	PMID:17924340	PCS					P	HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0005160	PMID:20413652	PCS	HP:0003577	5/5			P	HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0011536	PMID:20413652	PCS					P	HPO:skoehler[2013-09-30];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001629	OMIM:208530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001746	PMID:20413652	PCS		5/5			P	HPO:skoehler[2009-02-17];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001669	PMID:28991257	PCS		7/10			P	HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001636	PMID:28991257	PCS	HP:0003577	2/10			P	HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0000007	PMID:20413652	PCS					I	HPO:skoehler[2013-09-30];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001748	OMIM:208530	IEA					P	HPO:iea[2009-02-17]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0004935	PMID:20413652	PCS					P	HPO:skoehler[2013-09-30];HP:probinson[2019-03-01]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001642	OMIM:208530	IEA					P	HPO:iea[2009-02-17]
OMIM:208530	Right atrial isomerism (Ivemark)		HP:0001631	OMIM:208530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:136300	Flynn-Aird syndrome		HP:0002751	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0005700	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000670	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0004334	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0001387	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0001596	OMIM:136300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0001250	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0001251	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0002381	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0002293	OMIM:136300	TAS					P	HPO:skoehler[2015-12-30]
OMIM:136300	Flynn-Aird syndrome		HP:0000939	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000408	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000518	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000726	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0011001	OMIM:136300	IEA					P	HPO:iea[2012-08-03]
OMIM:136300	Flynn-Aird syndrome		HP:0009830	OMIM:136300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:136300	Flynn-Aird syndrome		HP:0002922	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000510	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000006	OMIM:136300	IEA					I	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000545	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:136300	Flynn-Aird syndrome		HP:0000962	OMIM:136300	IEA					P	HPO:iea[2009-02-17]
OMIM:610188	Joubert syndrome 5		HP:0003774	PMID:16682973	PCS	HP:0003621	11/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0000480	PMID:16682973	PCS	HP:0003577	2/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0001252	OMIM:610188	IEA		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0002085	PMID:16682973	PCS		2/10			P	HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0001251	PMID:16682973;PMID:16682970	PCS		19/19			P	HPO:probinson[2022-09-29];HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0001290	OMIM:610188	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610188	Joubert syndrome 5		HP:0000639	PMID:16682973;PMID:16682970	PCS		11/21			P	HPO:probinson[2022-09-29];HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0000718	PMID:16682970	PCS		1/9			P	HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0000657	OMIM:610188	IEA		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0002419	PMID:16682970	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0007663	PMID:16682970	PCS					P	HPO:probinson[2022-09-29];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0002876	OMIM:610188	IEA					P	HPO:iea[2009-02-17]
OMIM:610188	Joubert syndrome 5		HP:0000510	PMID:16682970	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0002335	PMID:16682973	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0001249	PMID:16682973;PMID:16682970	PCS		15/17			P	HPO:probinson[2022-09-29];HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0000175	PMID:16682970	PCS		1/9			P	HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0002871	OMIM:610188	IEA					P	HPO:iea[2009-02-17]
OMIM:610188	Joubert syndrome 5		HP:0005565	PMID:16682970	PCS		1/8			P	HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0006817	PMID:16682973	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0001263	PMID:16682970	PCS		9/9			P	HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0002790	OMIM:610188	IEA					P	HPO:iea[2009-02-17]
OMIM:610188	Joubert syndrome 5		HP:0000090	OMIM:610188	IEA					P	HPO:iea[2009-02-17]
OMIM:610188	Joubert syndrome 5		HP:0000803	PMID:16682970	PCS		4/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0000508	PMID:16682970	PCS		1/9			P	HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0000007	PMID:16682973	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0004727	OMIM:610188	IEA					P	HPO:iea[2009-02-17]
OMIM:610188	Joubert syndrome 5		HP:0007875	PMID:16682973;PMID:16682970	PCS	HP:0003577	11/19			P	HPO:probinson[2022-09-29];HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:610188	Joubert syndrome 5		HP:0002404	OMIM:610188	TAS					P	HPO:probinson[2012-06-10]
OMIM:301500	Fabry disease		HP:0001155	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001014	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001250	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0000083	PMID:19473999	PCS	HP:0011462	134/699	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0000083	PMID:19473999	PCS	HP:0011462	21/754	FEMALE		P	HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0001131	OMIM:301500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301500	Fabry disease		HP:0003394	OMIM:301500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:301500	Fabry disease		HP:0002380	OMIM:301500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:301500	Fabry disease		HP:0012702	OMIM:301500	TAS					P	HPO:skoehler[2014-03-24]
OMIM:301500	Fabry disease		HP:0011675	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001071	PMID:8993949	PCS					P	HPO:probinson[2022-11-10]
OMIM:301500	Fabry disease		HP:0012332	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001903	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0033595	PMID:17073606	PCS					P	HPO:probinson[2021-02-13]
OMIM:301500	Fabry disease		HP:0002018	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001004	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0006536	OMIM:301500	IEA				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:301500	Fabry disease		HP:0002014	OMIM:301500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301500	Fabry disease		HP:0003621	OMIM:301500	IEA					C	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0003401	OMIM:301500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301500	Fabry disease		HP:0002013	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001681	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0005144	PMID:19473999	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0000093	PMID:19473999	PCS		332/699	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0000093	PMID:19473999	PCS		246/754	FEMALE		P	HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0034864	OMIM:301500	TAS					P	HPO:probinson[2024-02-27]
OMIM:301500	Fabry disease		HP:0032567	PMID:26124059	PCS					P	HPO:probinson[2019-09-07]
OMIM:301500	Fabry disease		HP:0032568	PMID:28593486	PCS	HP:0003584				P	HPO:probinson[2019-09-07]
OMIM:301500	Fabry disease		HP:0001419	PMID:19473999	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0000822	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001658	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001635	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0001712	PMID:19473999	PCS		284/699	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0001712	PMID:19473999	PCS		180/754	FEMALE		P	HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0000823	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0000966	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:301500	Fabry disease		HP:0002326	PMID:19473999	PCS	HP:0003596	60/699	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0002326	PMID:19473999	PCS		46/754	FEMALE		P	HPO:probinson[2022-03-30]
OMIM:301500	Fabry disease		HP:0002027	OMIM:301500	IEA					P	HPO:iea[2009-02-17]
OMIM:132600	Pilomatrixoma, somatic		HP:0030434	PMID:10192393	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2020-07-20]
OMIM:132600	Pilomatrixoma, somatic		HP:0001442	PMID:10192393	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-07-20]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0030731	OMIM:305000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000486	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0004322	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002860	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0005212	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001251	OMIM:305000	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000085	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001809	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000518	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001807	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000953	OMIM:305000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0005528	OMIM:305000	TAS					P	HPO:skoehler[2013-09-30]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0008734	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002216	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001249	OMIM:305000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0009926	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000252	OMIM:305000	TAS					P	HPO:skoehler[2013-09-30]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0004334	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001263	PMID:33165394	PCS		0/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0012189	OMIM:305000	TAS					P	HPO:skoehler[2014-01-28]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001419	PMID:9590285	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0004808	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000648	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0012182	PMID:33165394	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0008404	PMID:33165394	PCS		3/3			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000047	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002745	PMID:33165394	PCS	HP:0025708	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001059	OMIM:305000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002863	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001596	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002043	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002165	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001394	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000939	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001903	OMIM:305000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000975	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000653	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000498	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001741	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0007427	PMID:33165394	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000670	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0003621	PMID:33165394	PCS		3/3			C	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001321	OMIM:305000	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001882	OMIM:305000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002091	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0006480	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000509	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0008661	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001511	OMIM:305000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002206	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001873	PMID:33165394	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0000028	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0001876	OMIM:305000	IEA					P	HPO:iea[2009-02-17]
OMIM:305000	Dyskeratosis congenita, X-linked		HP:0002721	OMIM:305000	TAS					P	HPO:skoehler[2013-09-30]
OMIM:137750	Glaucoma 1, open angle, A		HP:0007905	OMIM:137750	IEA					P	HPO:iea[2009-02-17]
OMIM:137750	Glaucoma 1, open angle, A		HP:0000006	OMIM:137750	IEA					I	HPO:iea[2009-02-17]
OMIM:137750	Glaucoma 1, open angle, A		HP:0000501	OMIM:137750	IEA					P	HPO:iea[2009-02-17]
OMIM:137750	Glaucoma 1, open angle, A		HP:0000545	OMIM:137750	IEA					P	HPO:iea[2009-02-17]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000483	PMID:33308444	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000486	PMID:33308444	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001156	PMID:33308444	PCS		12/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0030674	PMID:33308444	PCS		8/11			C	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001252	PMID:33308444	PCS		2/14			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0011675	PMID:33308444	PCS		1/14			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0011318	PMID:33308444	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0011062	PMID:33308444	PCS		3/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000639	PMID:33308444	PCS		2/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0012471	PMID:33308444	PCS		7/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0006297	PMID:33308444	PCS		4/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000678	PMID:33308444	PCS		12/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0008897	PMID:33308444	PCS		15/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000878	PMID:33308444	PCS		4/13			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001249	PMID:33308444	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000677	PMID:33308444	PCS		2/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0003026	PMID:33308444	PCS		6/11			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000252	PMID:33308444	PCS		9/13			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000175	PMID:33308444	PCS		1/14			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0003189	PMID:33308444	PCS		13/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0004279	PMID:33308444	PCS		12/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0002650	PMID:33308444	PCS		6/13			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000276	PMID:33308444	PCS		14/14			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000331	PMID:33308444	PCS		14/14			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001387	PMID:33308444	PCS		3/8			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0002299	PMID:33308444	PCS		2/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001382	PMID:33308444	PCS		2/8			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001263	PMID:33308444	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000426	PMID:33308444	PCS		13/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000668	PMID:33308444	PCS		2/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0200136	PMID:33308444	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000007	PMID:33308444	PCS					I	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000348	PMID:33308444	PCS		15/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000307	PMID:33308444	PCS		11/13			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001511	PMID:33308444	PCS		8/11			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000201	PMID:33308444	PCS		2/14			P	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001631	PMID:33308444	PCS		2/14			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000047	PMID:33308444	PCS		1/8	MALE		P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000325	PMID:33308444	PCS		14/14			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0002786	PMID:33308444	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619184	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001655	PMID:33308444	PCS		1/14			P	HPO:probinson[2021-04-27]
OMIM:608089	Endometrial carcinoma, somatic		HP:0001442	OMIM:608089	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:608089	Endometrial carcinoma, somatic		HP:0012114	OMIM:608089	TAS					P	HPO:skoehler[2013-01-09]
OMIM:608089	Endometrial carcinoma, somatic		HP:0000006	OMIM:608089	TAS					I	HPO:probinson[2020-07-17]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000343	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0002783	OMIM:615966	TAS				HP:0031796	P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0001250	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0003593	PMID:19075392	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0012444	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0012176	PMID:19075392	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-11]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0011220	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000219	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0003429	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0001302	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0001320	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0005403	PMID:19075392	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000252	OMIM:615966	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000054	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000431	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0002079	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000331	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000490	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0004430	PMID:19075392	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-11]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0010976	PMID:19075392	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0010557	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0011107	OMIM:615966	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000407	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000007	PMID:19075392	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000505	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0001511	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0000369	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		HP:0009879	OMIM:615966	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:300636	Immunodeficiency 33		HP:0002850	PMID:15833888	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:300636	Immunodeficiency 33		HP:0000684	PMID:18179816	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-16]
OMIM:300636	Immunodeficiency 33		HP:0032283	PMID:16818673	PCS					P	HPO:probinson[2020-07-25]
OMIM:300636	Immunodeficiency 33		HP:0001419	PMID:16818673	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-25]
OMIM:300636	Immunodeficiency 33		HP:0002718	PMID:15833888	PCS		2/2			P	HPO:skoehler[2015-08-22];HPO:probinson[2020-07-25]
OMIM:300636	Immunodeficiency 33		HP:0003593	PMID:18179816	PCS		1/1			C	HPO:probinson[2022-08-16]
OMIM:300636	Immunodeficiency 33		HP:0000668	PMID:15833888;PMID:18179816	PCS		1/3			P	HPO:probinson[2022-08-16];HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:300636	Immunodeficiency 33		HP:0003261	PMID:15833888	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:300636	Immunodeficiency 33		HP:0020102	PMID:18179816	PCS		1/1			P	HPO:probinson[2022-08-16];HPO:probinson[2022-08-16]
OMIM:300636	Immunodeficiency 33		HP:0002721	PMID:18179816	PCS		1/1			P	HPO:skoehler[2015-08-22];HPO:probinson[2022-08-16]
OMIM:300636	Immunodeficiency 33		HP:0000698	PMID:15833888;PMID:16818673	PCS		4/5			P	HPO:probinson[2020-07-25];HPO:skoehler[2017-07-13];HPO:probinson[2020-07-25]
OMIM:300622	Tn polyagglutination syndrome		HP:0002960	OMIM:300622	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300622	Tn polyagglutination syndrome		HP:0001442	OMIM:300622	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:300622	Tn polyagglutination syndrome		HP:0001877	OMIM:300622	IEA					P	HPO:skoehler[2013-01-11]
OMIM:200150	Choreoacanthocytosis		HP:0002069	PMID:28446873	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0003477	PMID:28446873	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0003236	PMID:28446873	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0003676	OMIM:200150	TAS					C	HPO:skoehler[2012-10-17]
OMIM:200150	Choreoacanthocytosis		HP:0003596	PMID:28446873	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0001332	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0002340	PMID:28446873	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0001250	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0001252	PMID:28446873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0003690	OMIM:200150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200150	Choreoacanthocytosis		HP:0100033	OMIM:200150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200150	Choreoacanthocytosis		HP:0000716	PMID:28446873	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0000718	OMIM:200150	TAS					P	HPO:skoehler[2013-02-25]
OMIM:200150	Choreoacanthocytosis		HP:0011462	PMID:28446873	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0001927	PMID:28446873	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0000739	PMID:28446873	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0000734	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0000712	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0025435	PMID:28446873	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0000751	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0007326	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0003763	PMID:28446873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0001265	PMID:28446873	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0003202	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0002015	PMID:28446873	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0006956	PMID:28446873	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0001300	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0002310	PMID:28446873	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0001761	OMIM:200150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200150	Choreoacanthocytosis		HP:0001260	PMID:28446873	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0001284	PMID:28446873	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:200150	Choreoacanthocytosis		HP:0002072	PMID:28446873	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0000709	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0000726	OMIM:200150	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0000007	PMID:28446873	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0002307	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:200150	Choreoacanthocytosis		HP:0000741	PMID:28446873	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0008767	PMID:28446873	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-10]
OMIM:200150	Choreoacanthocytosis		HP:0000763	OMIM:200150	IEA					P	HPO:iea[2009-02-17]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002300	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002067	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0003596	PMID:27423618	PCS		1/3			C	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002186	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002362	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0001250	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0003474	PMID:27423618	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002063	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002283	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0033051	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0034381	PMID:27423618	PCS					P	HPO:probinson[2022-09-05];HPO:probinson[2022-09-05]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0000716	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0025710	PMID:27423618	PCS		2/3			C	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0001268	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0007305	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0001347	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002015	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0001300	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002354	PMID:27423618	PCS		3/3			P	HPO:probinson[2012-07-18];HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0001288	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002352	OMIM:221820	IEA					P	HPO:skoehler[2015-01-27]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0001260	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0003581	OMIM:221820	TAS					C	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002171	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002172	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0000708	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0007371	PMID:27423618	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0000727	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002529	OMIM:221820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0008765	PMID:27423618	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0000746	PMID:27423618	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0001257	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0002500	OMIM:221820	TAS					P	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0000006	OMIM:221820	TAS					I	HPO:probinson[2012-07-18]
OMIM:221820	Leukoencephalopathy, diffuse hereditary, with spheroids		HP:0003678	OMIM:221820	TAS					C	HPO:skoehler[2012-10-17]
OMIM:615972	Nanophthalmos 4		HP:0003577	PMID:21345985	PCS		9/9			C	HPO:probinson[2022-11-01]
OMIM:615972	Nanophthalmos 4		HP:0000540	PMID:21345985	PCS		9/9			P	HPO:probinson[2022-11-01]
OMIM:615972	Nanophthalmos 4		HP:0012426	OMIM:615972	TAS		HP:0040283			P	HPO:skoehler[2014-09-21]
OMIM:615972	Nanophthalmos 4		HP:0000568	PMID:21345985	PCS	HP:0003577	9/9			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-11-01]
OMIM:615972	Nanophthalmos 4		HP:0007663	PMID:21345985	PCS		9/9			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-11-01]
OMIM:615972	Nanophthalmos 4		HP:0012109	PMID:21345985	PCS	HP:0003596	3/9			P	HPO:probinson[2022-11-01]
OMIM:615972	Nanophthalmos 4		HP:0000006	PMID:21345985	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-01]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0003577	PMID:27558376	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0003621	PMID:34089223	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0000365	PMID:27558376	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0031936	PMID:27558376	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0001272	PMID:27558376	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0002186	PMID:27558376	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0001251	PMID:27558376	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0002490	PMID:27558376	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0100543	PMID:27558376;PMID:34089223	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0007141	PMID:27558376;PMID:34089223	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0000639	PMID:27558376	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0000529	PMID:27558376	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0011463	PMID:27558376	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0000007	PMID:27558376	PCS					I	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0000648	PMID:27558376	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0002317	PMID:34089223	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0002505	PMID:27558376	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620711	Leukoencephalopathy, porphyria-related		HP:0002313	PMID:27558376;PMID:34089223	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:148190	Keratitis, hereditary		HP:0007759	OMIM:148190	IEA					P	HPO:iea[2009-02-17]
OMIM:148190	Keratitis, hereditary		HP:0000491	OMIM:148190	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148190	Keratitis, hereditary		HP:0000006	OMIM:148190	IEA					I	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0000132	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0030138	PMID:8282784	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0003540	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0003010	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0031364	PMID:8282784	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0002170	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0031126	PMID:2014236	PCS		12/12			P	HP:probinson[2019-01-22];HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0011873	PMID:8282784	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0011871	PMID:8282784	PCS		0/1			P	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0000979	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0008320	PMID:8282784	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0000007	OMIM:273800	TAS					I	HPO:probinson[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0100309	PMID:8282784	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0000978	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0008148	PMID:8282784	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0002239	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:273800	Glanzmann thrombasthenia		HP:0000421	PMID:8282784	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0004866	PMID:8282784;PMID:2014236	PCS		13/13			P	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0001975	PMID:2014236	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0003623	PMID:8282784	PCS		1/1			C	HPO:probinson[2022-04-30]
OMIM:273800	Glanzmann thrombasthenia		HP:0000225	OMIM:273800	IEA					P	HPO:iea[2009-02-17]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000343	PMID:26908619	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000189	PMID:26908619	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0002089	PMID:26908619	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0002980	PMID:26908619	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0030674	PMID:26908619	PCS		5/5			C	HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001629	PMID:26908619	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000778	PMID:26908619	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001789	PMID:26908619	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001989	PMID:26908619	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000218	PMID:26908619	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000774	PMID:26908619	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000158	PMID:26908619	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001562	PMID:26908619	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000473	PMID:26908619	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0003026	PMID:26908619	PCS		4/4			P	HPO:probinson[2022-11-24];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000494	PMID:26908619	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001762	PMID:26908619	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001640	PMID:26908619	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0025258	PMID:26908619	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000470	PMID:26908619	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001181	PMID:26908619	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0010557	PMID:26908619	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000007	PMID:26908619	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001539	PMID:26908619	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0001511	PMID:26908619	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0002623	PMID:26908619	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000444	PMID:26908619	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0002943	PMID:26908619	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000347	PMID:26908619	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000369	PMID:26908619	PCS		1/4			P	HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0000885	PMID:26908619	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-24]
OMIM:617022	Lethal congenital contracture syndrome 10		HP:0003557	PMID:26908619	PCS		1/3			P	HPO:probinson[2022-11-24]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0008936	PMID:27164683	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0000253	PMID:27164683	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0002510	OMIM:251280	IEA					P	HPO:iea[2009-02-17]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0002521	PMID:27164683	PCS		1/3			P	HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0001332	PMID:27164683	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0002123	OMIM:251280	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0002266	PMID:27164683	PCS		3/3			P	HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0001250	PMID:27164683	PCS		3/3			P	HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0030674	PMID:27164683	PCS		6/6			C	HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0001263	PMID:27164683	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0003593	OMIM:251280	IEA					C	HPO:iea[2009-02-17]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0012469	PMID:27164683	PCS		1/3			P	HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0032792	PMID:27164683	PCS		1/3			P	HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0011451	PMID:27164683	PCS		6/6			P	HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0000007	PMID:27164683	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0000505	PMID:27164683	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0001511	PMID:27164683	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-07]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0001347	OMIM:251280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251280	Microcephaly, seizures, spasticity, and brain calcifications		HP:0001622	PMID:27164683	PCS		2/6			P	HPO:probinson[2023-06-07]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0005227	PMID:16951683	PCS		1/10			P	HPO:probinson[2022-06-05]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0003596	PMID:16951683	PCS		2/4			C	HPO:probinson[2022-06-05]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0006716	PMID:16951683	PCS					P	HPO:skoehler[2013-01-10];HPO:probinson[2022-06-05]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0003003	PMID:16951683	PCS		2/10			P	HPO:probinson[2022-06-05]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0003584	PMID:16951683	PCS		1/4			C	HPO:probinson[2022-06-05]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0025710	PMID:16951683	PCS		1/4			C	HPO:probinson[2022-06-05];HPO:probinson[2022-06-05]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0012114	PMID:16951683	PCS		1/9			P	HPO:probinson[2022-06-05]
OMIM:613244	Colorectal cancer, hereditary nonpolyposis, type 8		HP:0000006	PMID:16951683	PCS					I	HPO:probinson[2022-06-05]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003445	OMIM:271150	IEA					P	HPO:iea[2009-02-17]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0002378	PMID:7658877	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003687	PMID:7658877	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0002398	OMIM:271150	IEA					P	HPO:iea[2009-02-17]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0009050	PMID:7658877	PCS		5/6			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0034045	PMID:7658877	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0011462	PMID:7658877	PCS		6/6			C	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0008981	PMID:7658877	PCS		3/6			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0000007	PMID:7658877	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003805	PMID:7658877	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0001308	PMID:7658877	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0002515	PMID:7658877	PCS		3/6			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0007126	OMIM:271150	IEA					P	HPO:iea[2009-02-17]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0007269	PMID:7658877	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003803	PMID:7658877	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003701	PMID:7658877	PCS		6/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003713	PMID:7658877	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0002522	OMIM:271150	IEA					P	HPO:iea[2009-02-17]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003677	PMID:7658877	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:271150	Spinal muscular atrophy, type IV		HP:0003557	PMID:7658877	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:102660	Adamantinoma of long bones		HP:0002664	OMIM:102660	IEA					P	HPO:iea[2009-02-17]
OMIM:102660	Adamantinoma of long bones		HP:0000006	OMIM:102660	IEA					I	HPO:iea[2009-02-17]
OMIM:618477	URIDINE-CYTIDINEURIA		HP:0032573	PMID:30847922	PCS					P	HPO:probinson[2020-03-14]
OMIM:618477	URIDINE-CYTIDINEURIA		HP:0032574	PMID:30847922	PCS					P	HPO:probinson[2020-03-14]
OMIM:618477	URIDINE-CYTIDINEURIA		HP:0000007	PMID:30847922	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2020-03-14]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0004322	PMID:29018201	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0002783	PMID:29018201	PCS		4/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0003593	PMID:29018201	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001508	PMID:29018201	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0011342	PMID:29018201	PCS		4/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001609	PMID:29018201	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001647	PMID:29018201	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0020222	PMID:29018201	PCS		3/4			P	HPO:probinson[2022-10-06]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001324	PMID:29018201	PCS		2/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0002315	PMID:29018201	PCS		2/3			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0004313	PMID:29018201	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0000750	PMID:29018201	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0003388	PMID:29018201	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0002750	PMID:29018201	PCS		2/3			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0011968	PMID:29018201	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0002352	PMID:29018201	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001581	PMID:29018201	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0012101	PMID:29018201	PCS		4/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0500152	PMID:29018201	PCS		2/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001511	PMID:29018201	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001510	PMID:29018201	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001631	PMID:29018201	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0001337	PMID:29018201	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0002720	PMID:29018201	PCS		1/4			P	HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0000006	PMID:29018201	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-04]
OMIM:617744	Immunodeficiency, developmental delay, and hypohomocysteinemia		HP:0002721	PMID:29018201	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0003577	PMID:31645653	PCS		1/1			C	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0000483	PMID:34515416	PCS		3/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001250	PMID:34515416	PCS		2/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001252	PMID:31645653	PCS		1/1			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0002020	PMID:34515416	PCS		4/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001270	PMID:34515416	PCS		9/11			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0040261	PMID:34515416	PCS		12/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001629	PMID:34515416	PCS		1/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0011220	PMID:31645653	PCS		1/1			P	HPO:probinson[2022-04-02];HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0000678	PMID:34515416	PCS		5/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0006532	PMID:34515416	PCS		3/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0006335	PMID:34515416	PCS		1/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001643	PMID:31645653	PCS	HP:0003623	1/1			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001643	PMID:34515416	PCS		1/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0000256	PMID:34515416;PMID:31645653	PCS		12/13			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001249	PMID:34515416;PMID:31645653	PCS		13/13			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001601	PMID:34515416	PCS		2/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0002036	PMID:34515416	PCS		1/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0025352	PMID:31645653	PCS					I	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0000750	PMID:34515416;PMID:31645653	PCS		10/13			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0011968	PMID:34515416	PCS		1/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0011904	PMID:34515416	PCS		4/5			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001263	PMID:31645653	PCS		1/1			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0010535	PMID:31645653	PCS	HP:0003593	1/1			P	HPO:probinson[2022-04-02];HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0010535	PMID:34515416	PCS		9/11			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0000729	PMID:34515416	PCS		7/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001537	PMID:31645653	PCS	HP:0003577	1/1			P	HPO:probinson[2022-04-02];HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001537	PMID:34515416	PCS		3/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0025502	PMID:34515416	PCS		7/10			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0002788	PMID:34515416	PCS		10/11			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0001631	PMID:34515416	PCS		2/12			P	HPO:probinson[2022-04-02]
OMIM:619769	Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin		HP:0000006	PMID:34515416	PCS					I	HPO:probinson[2022-04-02];HPO:probinson[2022-04-02]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0007957	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0010804	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0011819	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0002188	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0002263	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001252	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0012745	PMID:15057987;PMID:11337748	PCS		3/4			P	HPO:probinson[2022-02-09];HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0045074	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0009381	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000639	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000319	PMID:15057987;PMID:11337748	PCS		3/4			P	HPO:probinson[2022-02-09];HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000957	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0011341	PMID:15057987	PCS		2/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0011461	PMID:15057987	PCS		2/2			C	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000316	PMID:15057987;PMID:11337748	PCS		3/4			P	HPO:probinson[2022-02-09];HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000996	PMID:11337748	PCS		1/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001249	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000358	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000677	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000175	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000252	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000171	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0100380	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001263	PMID:15057987	PCS		2/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0005144	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0011927	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0010752	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000407	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000568	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000007	PMID:15057987	PCS					I	HPO:probinson[2024-08-03]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0004209	PMID:15057987;PMID:11337748	PCS		3/4			P	HPO:probinson[2022-02-09];HPO:probinson[2022-02-09];HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000201	PMID:15057987;PMID:11337748	PCS		4/4			P	HP:probinson[2022-02-09];HPO:probinson[2022-02-09];HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000369	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0003577	PMID:11337748	PCS		2/2			C	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001792	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000343	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0002000	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001629	PMID:11337748	PCS		1/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001508	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000414	PMID:15057987;PMID:11337748	PCS		3/4			P	HPO:probinson[2022-02-09];HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0009246	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000337	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000218	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0002711	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001562	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000750	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000430	PMID:15057987;PMID:11337748	PCS		4/4			P	HPO:probinson[2022-02-09];HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000232	PMID:15057987	PCS		2/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0005487	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000506	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000426	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000664	PMID:11337748	PCS		2/2			P	HPO:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0001511	PMID:15057987	PCS		1/2			P	HP:probinson[2022-02-09]
OMIM:608670	Robin sequence, distinctive facial appearance, and brachydactyly		HP:0000347	PMID:15057987;PMID:11337748	PCS		4/4			P	HPO:probinson[2022-02-09];HP:probinson[2022-02-09]
OMIM:618463	Hypoalphalipoproteinemia, primary, 2		HP:0003233	PMID:8282791	PCS		5/5			P	HPO:probinson[2022-05-10]
OMIM:618463	Hypoalphalipoproteinemia, primary, 2		HP:0000518	PMID:8282791	PCS		1/5			P	HPO:probinson[2022-05-10]
OMIM:618463	Hypoalphalipoproteinemia, primary, 2		HP:0001084	PMID:8282791	PCS		1/5			P	HPO:probinson[2022-05-10]
OMIM:618463	Hypoalphalipoproteinemia, primary, 2		HP:0011462	PMID:8282791	PCS		5/5			C	HPO:probinson[2022-05-10]
OMIM:618463	Hypoalphalipoproteinemia, primary, 2		HP:0010874	PMID:8282791	PCS		1/5			P	HPO:probinson[2022-05-10]
OMIM:618463	Hypoalphalipoproteinemia, primary, 2		HP:0000007	PMID:8282791	IEA					I	HPO:probinson[2022-05-10]
OMIM:618463	Hypoalphalipoproteinemia, primary, 2		HP:0005181	PMID:8282791	PCS		2/5			P	HPO:probinson[2022-05-10]
OMIM:146750	Ichthyosis, lamellar, autosomal dominant		HP:0000989	OMIM:146750	IEA					P	HPO:iea[2009-02-17]
OMIM:146750	Ichthyosis, lamellar, autosomal dominant		HP:0007479	OMIM:146750	TAS					P	HPO:skoehler[2012-09-10]
OMIM:146750	Ichthyosis, lamellar, autosomal dominant		HP:0000006	OMIM:146750	IEA					I	HPO:iea[2009-02-17]
OMIM:146750	Ichthyosis, lamellar, autosomal dominant		HP:0000962	OMIM:146750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002069	PMID:26675814	PCS		1/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002540	PMID:29449720	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001332	PMID:29449720	PCS		0/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002066	PMID:29449720	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001252	PMID:26675814	PCS		2/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0003196	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002460	PMID:29449720	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0003593	PMID:29449720	PCS		3/3			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0033048	PMID:26675814	PCS		3/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0033049	PMID:26675814	PCS		3/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0045075	PMID:29449720	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000518	PMID:26675814	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0011463	PMID:26675814	PCS		3/3			C	HPO:probinson[2022-09-07];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001324	PMID:26675814	PCS		2/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001249	PMID:26675814	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001188	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000252	PMID:29449720	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001266	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002079	PMID:29449720	PCS		2/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001387	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001382	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001263	PMID:26675814	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0034353	PMID:29449720	PCS		1/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000007	PMID:26675814	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000648	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000768	PMID:26675814	PCS		1/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000207	PMID:29449720	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000369	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001337	PMID:26675814	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000341	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001310	PMID:26675814	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001270	PMID:29449720	PCS		3/3		HP:0012828	P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0008070	PMID:29449720	PCS		1/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001508	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001305	PMID:29449720	PCS		1/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000411	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000653	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001348	PMID:29449720	PCS		2/2			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0006855	PMID:26675814	PCS		3/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002136	PMID:26675814	PCS		3/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002213	PMID:26675814	PCS		3/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002650	PMID:26675814;PMID:29449720	PCS		5/6			P	HPO:probinson[2022-09-07];HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0001762	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002299	PMID:26675814	PCS		3/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0011344	PMID:29449720	PCS		3/3			P	HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0005280	PMID:29449720	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0002808	PMID:29449720	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000505	PMID:29449720	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:617988	Jaberi-Elahi syndrome		HP:0000545	PMID:26675814	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0001561	PMID:27120771	PCS					P	HPO:probinson[2017-06-25]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0003113	OMIM:300971	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0001563	OMIM:300971	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0012408	PMID:27120771	PCS					P	HPO:probinson[2017-06-25]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0000848	OMIM:300971	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0001419	PMID:27120771	PCS					I	HPO:probinson[2017-06-25]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0002902	OMIM:300971	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0002150	PMID:27120771	PCS					P	HPO:probinson[2017-06-25]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0002900	OMIM:300971	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0000103	PMID:27120771	PCS					P	HPO:probinson[2017-06-25]
OMIM:300971	Bartter syndrome, type 5, antenatal, transient		HP:0001622	OMIM:300971	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0000662	PMID:9888420	PCS	HP:0011463	2/2			P	HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0000552	PMID:9888420	PCS		2/2			P	HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0000482	OMIM:615147	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0030825	PMID:9888420	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0200070	OMIM:615147	TAS					P	HPO:skoehler[2013-05-31]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0040137	PMID:9888420	PCS		2/2			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0011463	PMID:9888420	PCS		2/2			C	HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0031032	PMID:9888420	PCS		2/2			P	HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0000007	OMIM:615147	TAS					I	HPO:skoehler[2013-05-07]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0000612	PMID:9888420	PCS		2/2			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0007663	PMID:9888420	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0000505	OMIM:615147	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0001643	OMIM:615147	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0007502	PMID:9888420	PCS		2/2			P	HPO:probinson[2023-03-12]
OMIM:615147	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome		HP:0000556	OMIM:615147	TAS					P	HPO:skoehler[2013-06-06]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001771	PMID:21282593	PCS		5/8			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0030237	PMID:21282593	PCS		2/8			P	HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0003431	PMID:21282593	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001310	OMIM:302800	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001272	OMIM:302800	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002385	OMIM:302800	IEA					P	HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002460	OMIM:302800	TAS		20/20			P	HPO:skoehler[2012-11-21];HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001270	PMID:21282593	PCS		3/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0000639	OMIM:302800	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0040078	OMIM:302800	TAS					P	HPO:skoehler[2014-11-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0003829	OMIM:302800	IEA					I	HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002936	PMID:21282593	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001423	PMID:8266101	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002359	PMID:21282593	PCS		4/8			P	HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0007149	PMID:21282593	PCS		5/8			P	HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001265	OMIM:302800	IEA					P	HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002311	OMIM:302800	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002015	OMIM:302800	IEA					P	HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002378	PMID:21282593	PCS		3/8			P	HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0003487	OMIM:302800	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001288	PMID:21282593;OMIM:302800	PCS		16/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-26];HPO:skoehler[2012-11-21]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001761	PMID:21282593	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002395	OMIM:302800	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001260	OMIM:302800	IEA					P	HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0003383	PMID:21282593	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0003380	PMID:21282593	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0009053	PMID:21282593	PCS		6/8			P	HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0000407	OMIM:302800	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0009830	OMIM:302800	TAS					P	HPO:skoehler[2012-11-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002427	OMIM:302800	IEA					P	HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0030051	PMID:21282593	PCS		3/8			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0000763	OMIM:302800	IEA					P	HPO:skoehler[2015-01-21]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0003438	PMID:21282593	PCS		7/8			P	HPO:probinson[2021-02-26]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0002500	OMIM:302800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0003677	OMIM:302800	TAS					C	HPO:skoehler[2014-02-25]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0001337	OMIM:302800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0000764	OMIM:302800	IEA					P	HPO:iea[2009-02-17]
OMIM:302800	Charcot-Marie-Tooth neuropathy, X-linked dominant, 1		HP:0008944	PMID:21282593	PCS		4/8			P	HPO:probinson[2021-02-26]
OMIM:180105	Retinitis pigmentosa 10		HP:0001133	PMID:26720483	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0007737	PMID:26720483	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0000662	PMID:26720483	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0031609	OMIM:180105	IEA					P	HPO:skoehler[2019-09-07]
OMIM:180105	Retinitis pigmentosa 10		HP:0003593	OMIM:180105	IEA					C	HPO:iea[2009-02-17]
OMIM:180105	Retinitis pigmentosa 10		HP:0011504	PMID:26720483	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0011463	PMID:26720483	PCS		1/1			C	HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0007663	PMID:26720483	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0000543	PMID:26720483	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0007787	OMIM:180105	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:180105	Retinitis pigmentosa 10		HP:0000510	PMID:26720483	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0007688	OMIM:180105	IEA					P	HPO:iea[2009-02-17]
OMIM:180105	Retinitis pigmentosa 10		HP:0007843	PMID:26720483	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:180105	Retinitis pigmentosa 10		HP:0000006	PMID:11875050	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-29]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0005037	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0003031	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0003182	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0001915	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0000407	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0000979	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0006394	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0002827	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0001905	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0000967	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0004859	OMIM:605432	IEA					P	HPO:skoehler[2015-12-30]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0004209	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0001159	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0002986	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0000006	OMIM:605432	IEA					I	HPO:iea[2009-02-17]
OMIM:605432	Radioulnar synostosis with amegakaryocytic thrombocytopenia		HP:0005548	OMIM:605432	IEA					P	HPO:iea[2009-02-17]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000286	PMID:28781842;PMID:17273969	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0002465	OMIM:610759	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001770	PMID:25655089	PCS		4/14			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000365	PMID:25655089	PCS		7/13			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001773	PMID:25655089;PMID:17273969	PCS		12/14			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0004322	PMID:17273969	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001052	PMID:25655089	PCS		1/12			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001250	PMID:25655089	PCS		3/12			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0002020	PMID:25655089;PMID:17273969	PCS		11/16			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0003593	PMID:28781842	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0010047	PMID:28781842	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0011463	PMID:28781842	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000319	PMID:25655089	PCS		10/15			P	HPO:skoehler[2018-10-08];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001647	PMID:25655089	PCS		2/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000954	PMID:25655089	PCS		5/14			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0009623	PMID:25655089	PCS	HP:0003577	12/16			P	HPO:probinson[2013-04-01];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0009623	PMID:28781842	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0009623	PMID:17273969	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001643	PMID:25655089	PCS	HP:0003577	1/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001642	PMID:25655089	PCS		4/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-19]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000278	PMID:28781842;PMID:17273969	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001007	PMID:28781842;PMID:25655089;PMID:17273969	PCS		16/18			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19];HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001249	PMID:25655089;PMID:17273969	PCS		14/14			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000358	PMID:25655089	PCS		3/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0002553	PMID:28781842;PMID:25655089;PMID:17273969	PCS		17/18			P	HPO:probinson[2013-01-09];HPO:probinson[2022-03-19];HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000175	PMID:25655089	PCS		1/14			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0030820	PMID:25655089	PCS		2/13			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000252	PMID:28781842;PMID:17273969	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000574	PMID:28781842;PMID:25655089;PMID:17273969	PCS		11/16			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000331	PMID:28781842;PMID:17273969	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0011968	PMID:28781842	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001263	PMID:28781842;PMID:17273969	PCS		3/3			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000691	PMID:25655089	PCS		2/9			P	HP:probinson[2019-02-20];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000294	PMID:28781842;PMID:25655089;PMID:17273969	PCS		9/17			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0004691	PMID:28781842	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0002194	PMID:28781842;PMID:17273969	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0010750	PMID:28781842;PMID:17273969	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0010044	PMID:28781842	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0011451	PMID:25655089	PCS	HP:0003577	5/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000965	PMID:28781842;PMID:25655089;PMID:17273969	PCS		6/16			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000527	PMID:28781842;PMID:25655089;PMID:17273969	PCS		18/19			P	HPO:probinson[2013-04-01];HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0004209	PMID:28781842;PMID:25655089;PMID:17273969	PCS		11/17			P	HPO:probinson[2013-04-01];HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000006	PMID:28781842;PMID:25655089	PCS		20/20			I	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000248	PMID:25655089	PCS		11/15			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000369	PMID:28781842;PMID:17273969	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000324	PMID:25655089	PCS		1/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001655	PMID:28781842	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000687	PMID:28781842	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000341	PMID:28781842;PMID:17273969	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001476	PMID:25655089	PCS		1/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000343	PMID:25655089	PCS		10/15			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000463	PMID:28781842;PMID:25655089;PMID:17273969	PCS		9/17			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001156	OMIM:610759	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0012368	PMID:25655089	PCS		1/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0012210	PMID:28781842	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0100543	OMIM:610759	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001508	PMID:28781842;PMID:17273969	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001629	PMID:25655089	PCS	HP:0003577	2/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000414	PMID:25655089	PCS		12/14			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0008872	PMID:28781842;PMID:25655089;PMID:17273969	PCS		11/16			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19];HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000579	PMID:25655089	PCS		4/12			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000219	PMID:25655089	PCS		13/16			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0007665	PMID:28781842	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0002714	PMID:28781842;PMID:25655089;PMID:17273969	PCS		10/18			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000218	PMID:28781842;PMID:25655089;PMID:17273969	PCS		7/14			P	HPO:probinson[2013-04-01];HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000455	PMID:28781842;PMID:17273969	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0002996	PMID:25655089;PMID:17273969	PCS		6/12			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000233	PMID:17273969	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000072	PMID:25655089	PCS		1/16			P	HP:probinson[2019-02-20];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0005484	PMID:25655089	PCS		12/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000470	PMID:28781842;PMID:25655089;PMID:17273969	PCS		7/16			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0005280	PMID:28781842;PMID:25655089;PMID:17273969	PCS		8/18			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0100874	OMIM:610759	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0011230	PMID:25655089	PCS		1/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000508	PMID:28781842;PMID:25655089;PMID:17273969	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-05-05];HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000426	PMID:17273969	PCS	HP:0003577	1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-19]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000426	PMID:28781842	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0009237	PMID:28781842;PMID:25655089	PCS		11/15			P	HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0002007	PMID:25655089	PCS		1/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001357	PMID:25655089	PCS		1/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0200055	PMID:25655089	PCS		11/14			P	HPO:probinson[2013-04-01];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000664	PMID:28781842;PMID:25655089;PMID:17273969	PCS		14/18			P	HPO:probinson[2013-04-01];HP:probinson[2019-02-20];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0001631	PMID:25655089	PCS	HP:0003577	4/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000028	PMID:25655089	PCS		2/16			P	HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000347	PMID:25655089	PCS		6/15			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-20]
OMIM:610759	Cornelia de Lange syndrome 3		HP:0000545	PMID:25655089	PCS		5/11			P	HPO:probinson[2013-04-01];HP:probinson[2019-02-20]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0002366	OMIM:607225	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0001771	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0005216	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0003676	PMID:12145748	PCS					C	HPO:skoehler[2014-04-13];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0000020	OMIM:607225	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0003593	PMID:12145748	PCS		6/15			C	HPO:probinson[2009-02-17];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0001270	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0011463	PMID:12145748	PCS		9/15			C	HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0000514	PMID:12145748;OMIM:607225	PCS		25/25			P	HPO:probinson[2021-11-11];HPO:skoehler[2015-12-30]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0001324	PMID:12145748	PCS	HP:0003621	15/15			P	HPO:skoehler[2014-04-13];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0000478	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0001347	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0002015	PMID:12145748	PCS	HP:0003621	15/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0002510	PMID:12145748	PCS	HP:0003621	15/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0002650	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0003487	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0001761	OMIM:607225	TAS					P	HPO:skoehler[2014-04-13]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0000271	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0001260	OMIM:607225	IEA					P	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0002492	OMIM:607225	TAS	HP:0003593				P	HPO:probinson[2013-11-23]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0000007	PMID:12145748	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0002425	PMID:12145748	PCS	HP:0003621	15/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0001258	PMID:12145748	PCS	HP:0011463	15/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-11]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0003677	OMIM:607225	IEA					C	HPO:iea[2009-02-17]
OMIM:607225	Spastic paralysis, infantile-onset ascending		HP:0002445	OMIM:607225	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609220	Bruck syndrome 2		HP:0002980	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0001762	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:6001098	PMID:15523624	PCS					P	HPO:probinson[2024-12-14]
OMIM:609220	Bruck syndrome 2		HP:0000023	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0004322	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0001371	OMIM:609220	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609220	Bruck syndrome 2		HP:0003080	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:6000807	PMID:31472299	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:609220	Bruck syndrome 2		HP:0006380	OMIM:609220	TAS	HP:0003577				P	HPO:probinson[2013-03-12]
OMIM:609220	Bruck syndrome 2		HP:0000938	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0000926	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0000007	OMIM:609220	IEA					I	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0002659	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0000768	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0002645	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:609220	Bruck syndrome 2		HP:0002987	OMIM:609220	TAS	HP:0003577				P	HPO:probinson[2013-03-12]
OMIM:609220	Bruck syndrome 2		HP:0001059	OMIM:609220	IEA					P	HPO:iea[2009-02-17]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0003038	PMID:25361962	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0003577	PMID:25361962	PCS		2/2			C	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0008905	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0002089	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0002023	OMIM:616300	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000089	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0001591	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000062	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0003177	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0003375	PMID:25361962	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0004482	PMID:25361962	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0002084	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0410030	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000280	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000180	PMID:25361962	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0045075	PMID:25361962	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0011315	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0010297	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0011340	PMID:25361962	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0003826	PMID:25361962	PCS		1/2			C	HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000316	PMID:25361962	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0002419	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0001305	PMID:25361962	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0001643	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000774	PMID:25361962	PCS		2/2			P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000773	PMID:25361962	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0003026	PMID:25361962	PCS		2/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000175	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000695	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0008839	PMID:25361962	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0001321	PMID:25361962	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0002692	OMIM:616300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0011800	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0002093	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0011802	PMID:25361962	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0003180	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0100259	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0100258	PMID:25361962	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000308	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000107	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000448	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000888	PMID:25361962	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000568	OMIM:616300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000007	PMID:25361962	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0001539	PMID:25361962	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000400	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0005736	PMID:25361962	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		HP:0000028	OMIM:616300	TAS					P	HPO:skoehler[2015-05-31]
OMIM:619033	Vissers-Bodmer syndrome		HP:0004325	PMID:32553196	PCS		6/31			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0000098	PMID:32553196	PCS		2/33			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0000750	PMID:32553196	PCS		29/35			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0004322	PMID:32553196	PCS		18/33			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001250	PMID:32553196	PCS		9/36			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001360	PMID:32553196	PCS		4/31			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001260	PMID:32553196	PCS		10/29			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001263	PMID:32553196	PCS		34/37			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001290	PMID:32553196	PCS		26/35			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001270	PMID:32553196	PCS		29/35			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001182	PMID:32553196	PCS		3/35			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0040195	PMID:32553196	PCS		7/34			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001999	PMID:32553196	PCS					P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001511	PMID:32553196	PCS		8/35			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0000006	PMID:32553196	PCS					I	HPO:probinson[2020-12-04];HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001249	PMID:32553196	PCS		23/32			P	HPO:probinson[2020-12-04]
OMIM:619033	Vissers-Bodmer syndrome		HP:0001622	PMID:32553196	PCS		6/38			P	HPO:probinson[2020-12-04]
OMIM:610017	Multiple synostoses syndrome 2		HP:0001762	OMIM:610017	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610017	Multiple synostoses syndrome 2		HP:0001156	OMIM:610017	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610017	Multiple synostoses syndrome 2		HP:0002948	PMID:16532400	PCS					P	HPO:probinson[2013-03-31]
OMIM:610017	Multiple synostoses syndrome 2		HP:0003041	OMIM:610017	TAS					P	HPO:probinson[2013-01-09]
OMIM:610017	Multiple synostoses syndrome 2		HP:0009700	PMID:16532400	PCS					P	HPO:probinson[2013-03-31]
OMIM:610017	Multiple synostoses syndrome 2		HP:0008368	PMID:16532400	PCS					P	HPO:probinson[2013-03-31]
OMIM:610017	Multiple synostoses syndrome 2		HP:0009702	PMID:16532400	PCS					P	HPO:probinson[2013-03-31]
OMIM:610017	Multiple synostoses syndrome 2		HP:0000006	PMID:16532400	PCS					I	HPO:probinson[2013-03-31]
OMIM:610017	Multiple synostoses syndrome 2		HP:0100264	OMIM:610017	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610017	Multiple synostoses syndrome 2		HP:0000445	PMID:16532400	PCS					P	HPO:probinson[2013-03-31]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0001385	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0009804	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0002136	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0004279	PMID:20358595	PCS				HP:0012825	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0002970	PMID:20358595	PCS		1/4			P	HPO:probinson[2012-07-17];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0005086	PMID:20358595	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0030839	PMID:20358595	PCS		3/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0011800	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0003071	PMID:20358595	PCS					P	HPO:skoehler[2013-04-14];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0010585	PMID:20358595	PCS					P	HPO:probinson[2016-02-01];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0012378	PMID:20358595	PCS		2/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0010886	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0100694	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0011463	PMID:20358595	PCS		4/4			C	HPO:probinson[2016-02-01];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0010582	PMID:20358595	PCS					P	HPO:probinson[2012-07-28];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0002515	PMID:20358595	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0025238	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0002656	PMID:20358595	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0005715	PMID:8528240	PCS					P	HPO:probinson[2021-02-26]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0002007	PMID:20358595	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0000006	PMID:8528240	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:600204	Epiphyseal dysplasia, multiple, 2		HP:0003502	PMID:20358595	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-08]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0003621	PMID:35066646	PCS		1/1			C	HPO:probinson[2022-04-09]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0030344	PMID:35066646	PCS		1/1			P	HPO:probinson[2022-04-09]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0008197	PMID:35066646	PCS		1/1			P	HPO:probinson[2022-04-09]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0030341	PMID:35066646	PCS		1/1			P	HPO:probinson[2022-04-09]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0000007	PMID:35066646	PCS					I	HPO:probinson[2022-04-09]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0000458	PMID:35066646	PCS		0/1			P	HPO:probinson[2022-04-09];HPO:probinson[2024-03-15]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0020159	PMID:35066646	PCS		1/1			P	HPO:probinson[2022-04-09]
OMIM:619755	Hypogonadotropic hypogonadism 27 without anosmia		HP:0001513	PMID:35066646	PCS		1/1			P	HPO:probinson[2022-04-09]
OMIM:207950	Chiari malformation type II		HP:0002179	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0005348	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0002015	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0002475	OMIM:207950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:207950	Chiari malformation type II		HP:0002483	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0011968	OMIM:207950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:207950	Chiari malformation type II		HP:0003396	OMIM:207950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:207950	Chiari malformation type II		HP:0001252	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0001274	OMIM:207950	IEA		HP:0040282			P	HPO:skoehler[2010-06-20]
OMIM:207950	Chiari malformation type II		HP:0001251	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0001290	OMIM:207950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:207950	Chiari malformation type II		HP:0002282	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0003690	OMIM:207950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:207950	Chiari malformation type II		HP:0012318	OMIM:207950	TAS					P	HPO:probinson[2013-08-10]
OMIM:207950	Chiari malformation type II		HP:0000639	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0002308	OMIM:207950	TAS					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0000238	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0001426	OMIM:207950	IEA					I	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0002318	OMIM:207950	IEA					P	HPO:iea[2009-02-17]
OMIM:207950	Chiari malformation type II		HP:0000961	OMIM:207950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:207950	Chiari malformation type II		HP:0002414	OMIM:207950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0002014	OMIM:614265	TAS					P	HPO:probinson[2013-08-10]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0001993	OMIM:614265	TAS					P	HPO:probinson[2013-08-10]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0002013	OMIM:614265	TAS					P	HPO:probinson[2013-08-10]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0001508	OMIM:614265	TAS					P	HPO:probinson[2013-08-10]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0001263	OMIM:614265	TAS					P	HPO:probinson[2013-08-10]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0012120	PMID:21841779	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0001944	OMIM:614265	TAS					P	HPO:probinson[2013-08-10]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0000007	PMID:21841779	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614265	Combined malonic and methylmalonic aciduria		HP:0011169	OMIM:614265	TAS					P	HPO:probinson[2013-08-10]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0002069	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0002312	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0002059	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0002353	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0001272	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0002384	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0002074	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0000737	OMIM:610003	TAS					P	HPO:probinson[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0000007	OMIM:610003	IEA					I	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0000711	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0001268	OMIM:610003	TAS					P	HPO:probinson[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0001249	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0003677	OMIM:610003	IEA					C	HPO:iea[2009-02-17]
OMIM:610003	Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant		HP:0003205	OMIM:610003	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0002983	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003577	PMID:14729840	PCS		2/2			C	HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0002089	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0008905	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0004565	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0001156	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0005257	PMID:14729840	PCS		2/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0005451	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003175	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003173	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000280	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0012368	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0200083	PMID:14729840	PCS		2/2			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0008452	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003826	PMID:14729840	PCS		1/2			C	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000774	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000256	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000773	OMIM:151210	TAS					P	HPO:probinson[2012-05-27]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003026	PMID:14729840	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0009826	PMID:14729840	PCS		2/2		HP:0012828	P	HPO:probinson[2012-05-05];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0001561	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003025	PMID:14729840	PCS		2/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003300	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0002098	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003021	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000470	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0002194	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0004591	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0011800	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0005280	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0003180	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000947	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000946	PMID:14729840	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0005619	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0005716	OMIM:151210	TAS					P	HPO:probinson[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0001538	PMID:14729840	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0008921	OMIM:151210	IEA					P	HPO:iea[2009-02-17]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0002986	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000883	OMIM:151210	TAS					P	HPO:probinson[2012-05-27]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000006	PMID:14729840	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:151210	Platyspondylic lethal skeletal dysplasia, Torrance type		HP:0000369	PMID:14729840	PCS		1/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:606661	Melanoma, uveal, susceptibility to, 2		HP:0007716	PMID:32002398	PCS					P	HPO:probinson[2022-08-28]
OMIM:606661	Melanoma, uveal, susceptibility to, 2		HP:0003581	PMID:32002398	PCS					C	HPO:probinson[2022-08-28]
OMIM:606661	Melanoma, uveal, susceptibility to, 2		HP:0000006	PMID:32002398	PCS					I	HPO:probinson[2022-08-28]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0003577	PMID:10562302	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0011968	PMID:10562302	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0003198	OMIM:616314	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0001252	OMIM:616314	TAS	HP:0003623				P	HPO:skoehler[2015-05-31]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0000007	PMID:10562302	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0001319	OMIM:616314	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0002093	PMID:10562302	PCS		3/3		HP:0025303	P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0001324	OMIM:616314	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0030208	PMID:10562302	PCS		0/1			P	HPO:probinson[2023-02-12]
OMIM:616314	Myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency		HP:0003403	PMID:10562302	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002389	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0007957	PMID:22742195	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001498	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002188	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002980	PMID:32227665	PCS		2/26			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0030137	PMID:14598347	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000486	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0006507	ISBN-13:978-3-7945-2657-4;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		50%			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0004322	ISBN-13:978-3-7945-2657-4	TAS		7%			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001250	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0005773	PMID:14598347	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0003396	PMID:32227665	PCS		1/26			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001051	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0003031	PMID:31579100	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000085	PMID:12471199;PMID:32227665	PCS		6/60			P	HPO:probinson[2022-07-01];HPO:skoehler[2012-11-16];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0100694	ISBN-13:978-0-12-383834-6;ISBN-13:978-3-7945-2657-4	PCS		4/20			P	HPO:iea[2018-03-13];HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000518	PMID:22742195	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0100327	PMID:12471199;PMID:32227665	PCS		17/49			P	HPO:probinson[2022-07-01];HPO:iea[2010-09-16];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0004717	OMIM:274000	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0009702	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001522	OMIM:274000;ISBN-13:978-3-7945-2657-4	TAS		40%			C	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001643	PMID:12471199	PCS		1/34			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002414	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000996	PMID:12471199	PCS		8/34			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001249	PMID:12471199	PCS		1/34			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0004712	PMID:14598347	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000891	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000175	PMID:12471199	PCS		1/34			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002673	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002990	PMID:32227665	PCS		1/26			P	HPO:iea[2010-10-01];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001263	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0003043	ISBN-13:978-3-7945-2657-4;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001181	PMID:14598347	PCS		1/1			P	HPO:iea[2010-09-16];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002827	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002949	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000007	PMID:32227665	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0006101	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0009777	PMID:32227665;PMID:22742195	PCS		0/27			P	HPO:probinson[2022-07-01];HPO:iea[2010-09-16];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001737	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0004209	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0009778	PMID:17236129	PCS		25/26			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000248	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0007514	PMID:32227665	PCS		1/26			P	HPO:iea[2010-10-01];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002984	PMID:32227665	PCS		8/26			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001974	ISBN-13:978-3-7945-2657-4	TAS		62%			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002245	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0003577	PMID:31579100;PMID:14598347;PMID:22742195;PMID:35463560	PCS		4/4			C	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0010946	PMID:12471199	PCS		1/34			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000463	OMIM:274000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001270	OMIM:274000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001629	PMID:12471199;PMID:14598347;PMID:17236129	PCS		5/61			P	HPO:probinson[2022-07-01];HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001903	PMID:35463560	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0009487	PMID:31579100	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0012098	PMID:32227665	PCS		1/26			P	HPO:iea[2012-08-20];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0009486	PMID:14598347	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0006695	PMID:12471199	PCS		1/34			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002999	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0008952	OMIM:274000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000895	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0004977	PMID:12471199;PMID:31579100;PMID:22742195;PMID:35463560;PMID:17236129	PCS		67/67			P	HPO:probinson[2022-07-01];HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0009803	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001320	PMID:14598347	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0004313	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001880	ISBN-13:978-3-7945-2657-4	TAS		HP:0040282			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000076	PMID:35463560	PCS		1/1			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0009829	ISBN-13:978-3-7945-2657-4;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001762	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001321	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0002970	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0003022	PMID:32227665	PCS		4/26			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000073	PMID:12471199	PCS		1/34			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000151	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001680	PMID:14598347	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000272	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0011304	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282			P	HPO:iea[2010-09-16]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000508	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001636	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0006443	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0007413	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001631	PMID:12471199	PCS		1/34			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001433	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-10-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0001873	PMID:12471199;PMID:31579100;PMID:14598347;PMID:32227665;PMID:22742195;PMID:35463560;PMID:17236129	PCS		78/82			P	HPO:probinson[2022-07-01];HPO:iea[2009-02-17]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0003974	PMID:32227665	PCS		21/26			P	HPO:probinson[2022-07-01]
OMIM:274000	Thrombocytopenia-absent radius syndrome		HP:0000347	OMIM:274000	TAS					P	HPO:skoehler[2012-11-16]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0003621	PMID:32707086	PCS		5/5			C	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0003676	PMID:32707086	PCS		5/5			C	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0003401	PMID:32707086	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0002015	PMID:32707086	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0003487	PMID:32707086	PCS		3/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0000012	PMID:32707086	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0002395	PMID:32707086	PCS		5/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0002066	PMID:32707086	PCS		2/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0003394	PMID:32707086	PCS		3/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0000007	PMID:32707086	PCS					I	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0002317	PMID:32707086	PCS	HP:0003621	5/5			P	HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0001258	PMID:32707086	PCS	HP:0003621	5/5			P	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619027	Spastic paraplegia 83, autosomal recessive		HP:0003326	PMID:32707086	PCS		1/5			P	HPO:probinson[2020-11-29]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0008936	PMID:30239721	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0002751	PMID:30239721	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0002188	PMID:30239721	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0001036	PMID:30239721	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0001263	PMID:30239721	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0003593	PMID:30239721	PCS		1/1			C	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0005484	PMID:30239721	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0001482	PMID:30239721	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0000817	PMID:30239721	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0100716	PMID:30239721	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0000713	PMID:30239721	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0000006	PMID:30239721	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:618339	Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development		HP:0000962	PMID:30239721	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:602361	Gracile bone dysplasia		HP:0003015	OMIM:602361	TAS					P	HPO:skoehler[2013-09-17]
OMIM:602361	Gracile bone dysplasia		HP:0000054	PMID:23684011	PCS		3/5			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0003577	PMID:23684011	PCS		5/5			C	HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0001541	OMIM:602361	TAS					P	HPO:skoehler[2013-09-17]
OMIM:602361	Gracile bone dysplasia		HP:0001156	OMIM:602361	TAS					P	HPO:skoehler[2014-11-26]
OMIM:602361	Gracile bone dysplasia		HP:0004322	PMID:23684011	PCS		5/5			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0001250	PMID:23684011	PCS		1/5			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0004331	OMIM:602361	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:602361	Gracile bone dysplasia		HP:0003100	PMID:23684011	TAS					P	HPO:skoehler[2015-03-21]
OMIM:602361	Gracile bone dysplasia		HP:0001263	PMID:23684011	PCS		1/1			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0006270	OMIM:602361	TAS					P	HPO:skoehler[2013-09-17]
OMIM:602361	Gracile bone dysplasia		HP:0001508	PMID:23684011	PCS		1/5		HP:0012828	P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0010296	OMIM:602361	TAS					P	HPO:skoehler[2013-09-17]
OMIM:602361	Gracile bone dysplasia		HP:0011220	OMIM:602361	TAS					P	HPO:skoehler[2013-09-17]
OMIM:602361	Gracile bone dysplasia		HP:0001746	PMID:23684011	PCS		1/5			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0000238	PMID:23684011	PCS		2/5			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0000568	PMID:23684011	PCS		1/5			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0000526	OMIM:602361	TAS					P	HPO:skoehler[2013-09-17]
OMIM:602361	Gracile bone dysplasia		HP:0002901	PMID:23684011	PCS		5/5			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0001522	PMID:23684011	PCS		4/5			C	HPO:probinson[2022-11-27]
OMIM:602361	Gracile bone dysplasia		HP:0000883	OMIM:602361	IEA					P	HPO:skoehler[2019-09-07]
OMIM:602361	Gracile bone dysplasia		HP:0000006	PMID:23684011	PCS					I	HPO:skoehler[2013-09-17];HPO:probinson[2022-11-27]
OMIM:239100	van Buchem disease		HP:0006824	OMIM:239100	IEA					P	HPO:iea[2009-02-17]
OMIM:239100	van Buchem disease		HP:0000365	OMIM:239100	IEA					P	HPO:iea[2009-02-17]
OMIM:239100	van Buchem disease		HP:0007958	OMIM:239100	IEA					P	HPO:iea[2009-02-17]
OMIM:239100	van Buchem disease		HP:0000935	OMIM:239100	IEA					P	HPO:iea[2009-02-17]
OMIM:239100	van Buchem disease		HP:0003155	OMIM:239100	IEA					P	HPO:iea[2009-02-17]
OMIM:239100	van Buchem disease		HP:0011001	OMIM:239100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239100	van Buchem disease		HP:0000007	OMIM:239100	IEA					I	HPO:iea[2009-02-17]
OMIM:239100	van Buchem disease		HP:0002315	OMIM:239100	IEA					P	HPO:iea[2009-02-17]
OMIM:239100	van Buchem disease		HP:6000749	PMID:23074140	PCS					P	HPO:probinson[2024-06-29]
OMIM:239100	van Buchem disease		HP:0004437	OMIM:239100	IEA					P	HPO:iea[2009-02-17]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0003487	OMIM:258501	IEA					P	HPO:iea[2009-02-17]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0003344	PMID:11668429	PCS		10/10			P	HPO:probinson[2020-10-20];HPO:probinson[2020-10-20]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0001260	OMIM:258501	IEA					P	HPO:iea[2009-02-17]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0001251	PMID:11668429	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0002072	OMIM:258501	IEA					P	HPO:iea[2009-02-17]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0002071	PMID:11668429	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0100543	OMIM:258501	IEA					P	HPO:iea[2009-02-17]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0000007	PMID:11668429	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0007663	OMIM:258501	TAS					P	HPO:skoehler[2015-07-26]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0000505	OMIM:258501	IEA					P	HPO:iea[2009-02-17]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0000648	PMID:11668429	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0001257	PMID:11668429	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0001347	OMIM:258501	IEA					P	HPO:iea[2009-02-17]
OMIM:258501	3-methylglutaconic aciduria, type III		HP:0003535	PMID:11668429	PCS		10/10			P	HPO:skoehler[2015-01-19];HPO:probinson[2020-10-20]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002301	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0003676	OMIM:612199	IEA					C	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002584	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001332	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0004322	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0010648	PMID:22267198	PCS		2/13			P	HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002164	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001250	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001251	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0003593	OMIM:612199	IEA					C	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002062	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0008070	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0100864	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0000939	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001903	PMID:22267198	PCS		5/13			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0000938	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0000618	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0008897	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0007763	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002857	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002659	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0004979	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0005528	OMIM:612199	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002216	PMID:22267198	PCS		3/12			P	HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002514	PMID:22267198	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002415	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001268	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002756	PMID:22267198	PCS		8/12			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002213	PMID:22267198	PCS		2/13			P	HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002650	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001260	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002352	PMID:22267198	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002071	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0007256	OMIM:612199	TAS					P	HPO:skoehler[2015-01-04]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0000007	PMID:22267198	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0006487	OMIM:612199	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0000648	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002604	PMID:22267198	PCS		6/13			P	HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001511	PMID:22267198	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0008404	PMID:22267198	PCS		5/13			P	HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0007898	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002745	OMIM:612199	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001257	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001873	OMIM:612199	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0002206	PMID:22267198	PCS		1/13			P	HPO:probinson[2023-02-18]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0000963	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:612199	Cerebroretinal microangiopathy with calcifications and cysts 1		HP:0001337	OMIM:612199	IEA					P	HPO:iea[2009-02-17]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0003202	PMID:20045102	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0003477	OMIM:613287	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0001265	PMID:22206013	PCS		3/7			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0003621	PMID:20045102	IEA		3/17			C	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0003596	PMID:20045102	PCS		2/17			C	HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0003431	OMIM:613287	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0001761	PMID:22009580	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0002460	PMID:20045102	PCS		15/15			P	HPO:skoehler[2013-05-29];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0001284	PMID:20045102	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0000407	OMIM:613287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0007340	PMID:22206013	PCS		4/7			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0011462	PMID:20045102	PCS		12/17			C	HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0009027	PMID:22009580	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0002936	PMID:22206013;PMID:20045102	PCS		17/22			P	HPO:probinson[2022-03-21];HPO:skoehler[2012-10-17];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0003438	PMID:22206013	IEA		4/7			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0000006	PMID:20045102	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0001765	PMID:22009580	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-21]
OMIM:613287	Charcot-Marie-Tooth disease, axonal, type 2N		HP:0008944	PMID:22206013	PCS		4/7			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:300018	Dosage-Sensitive sex reversal		HP:0012245	OMIM:300018	TAS					P	HPO:probinson[2013-04-02]
OMIM:300018	Dosage-Sensitive sex reversal		HP:0001417	OMIM:300018	TAS					I	HPO:probinson[2009-02-17]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0010628	OMIM:611490	TAS					P	HPO:probinson[2013-04-01]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0004576	OMIM:611490	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0003593	PMID:17033731	PCS		1/2			C	HPO:probinson[2022-10-10];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0002240	PMID:17033731	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0011002	PMID:11207362	PCS	HP:0003623	1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0011002	PMID:17033731	PCS		2/2			P	HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0011001	PMID:17033731	PCS		2/2			P	HPO:probinson[2022-10-10];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0011463	PMID:17033731	PCS		1/2			C	HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0001903	PMID:11207362	PCS	HP:0003623	1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0001903	PMID:17033731	PCS		1/1			P	HPO:probinson[2022-10-10];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0000007	PMID:11207362	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0000505	OMIM:611490	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0002757	OMIM:611490	TAS					P	HPO:probinson[2013-04-01]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0000967	PMID:17033731	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0000648	PMID:17033731	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0001923	OMIM:611490	TAS					P	HPO:probinson[2013-04-01]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0000543	PMID:17033731;OMIM:611490	PCS		11/12			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0001873	PMID:17033731	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0001510	OMIM:611490	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0001744	PMID:17033731	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:611490	Osteopetrosis, autosomal recessive 4		HP:0003623	PMID:11207362	PCS		1/1			C	HPO:probinson[2022-10-10]
OMIM:245550	Lambert syndrome		HP:0000154	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0000384	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0005248	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0001762	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0000023	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0000272	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0000007	OMIM:245550	IEA					I	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0000047	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:245550	Lambert syndrome		HP:0000952	OMIM:245550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:245550	Lambert syndrome		HP:0001249	OMIM:245550	IEA					P	HPO:iea[2009-02-17]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0032989	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0006956	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0010804	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0000343	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0000750	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0001762	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0001263	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0003593	PMID:29648665	PCS		1/1			C	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0002191	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0011344	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0040010	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0000508	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0000007	PMID:29648665	PCS					I	HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0200012	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0025336	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0001249	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619972	Neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy		HP:0000248	PMID:29648665	PCS		1/1			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:232900	Glycoprotein storage disease		HP:0000007	OMIM:232900	IEA					I	HPO:iea[2009-02-17]
OMIM:232900	Glycoprotein storage disease		HP:0001744	OMIM:232900	IEA					P	HPO:iea[2009-02-17]
OMIM:232900	Glycoprotein storage disease		HP:0001997	OMIM:232900	IEA					P	HPO:iea[2009-02-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002014	OMIM:607594	IEA					P	HPO:iea[2009-02-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002850	PMID:15507387	PCS		2/5			P	HPO:probinson[2009-02-17];HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0030388	PMID:12577056	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002110	OMIM:607594	IEA					P	HPO:iea[2009-02-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002240	OMIM:607594	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0011839	PMID:12577056	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-13]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002090	OMIM:607594	IEA					P	HPO:iea[2009-02-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0011840	OMIM:607594	IEA					P	HPO:iea[2009-02-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0010976	PMID:12577056	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0011108	OMIM:607594	IEA					P	HPO:iea[2012-05-06]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0001904	OMIM:607594	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0011463	PMID:15507387	PCS		2/5			C	HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0000509	OMIM:607594	TAS					P	HPO:probinson[2009-02-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0011462	PMID:15507387	PCS		3/5			C	HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002718	PMID:12577056	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0000007	PMID:12577056	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002716	OMIM:607594	IEA					P	HPO:iea[2009-02-17]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0000403	OMIM:607594	TAS					P	HPO:probinson[2012-05-06]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002837	OMIM:607594	TAS					P	HPO:skoehler[2012-11-21]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0006532	OMIM:607594	TAS					P	HPO:skoehler[2012-11-21]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002720	PMID:15507387	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0001744	PMID:12577056	PCS		0/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-13]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0004315	PMID:15507387	TAS		5/5			P	HPO:probinson[2012-05-06];HPO:probinson[2021-05-09]
OMIM:607594	Immunodeficiency, common variable, 1		HP:0002721	OMIM:607594	IEA					P	HPO:skoehler[2015-01-21]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0000750	PMID:29656860	PCS		2/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0001250	PMID:29656860	PCS		6/26			P	HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0011968	PMID:29656860	PCS		8/14			P	HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0000729	PMID:29656860	PCS		24/27			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0001263	PMID:29656860	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0000733	PMID:29656860	PCS		1/32			P	HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0001270	PMID:29656860	PCS		31/32			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0007018	PMID:29656860	PCS		1/28			P	HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0001249	PMID:29656860	PCS		23/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-07]
OMIM:617787	Intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities		HP:0000006	PMID:29656860	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2021-07-07]
OMIM:260920	Hyper-Igd syndrome		HP:0002840	PMID:32822427	PCS		8/10			P	HPO:probinson[2020-08-24];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0032638	PMID:21708801	PCS		33/33			P	HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0025143	PMID:8190036	PCS		38/50			P	HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0000662	PMID:16435210	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0002321	OMIM:260920	TAS					P	HPO:skoehler[2009-02-17]
OMIM:260920	Hyper-Igd syndrome		HP:0003593	PMID:21708801	PCS		30/50			C	HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0011897	PMID:8190036	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0045073	PMID:8190036	PCS		3/50			P	HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0032163	PMID:32822427	PCS		1/10			P	HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0002719	PMID:21708801	PCS		13/50			P	HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0002716	PMID:8190036;PMID:21708801	PCS		82/100			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-24];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0006772	PMID:21708801	PCS		3/50			P	HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0002315	PMID:8190036	PCS		26/50			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0000510	PMID:16435210	PCS		HP:0040283			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0001744	PMID:8190036;PMID:21708801	PCS		42/60			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-02];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0001369	PMID:8190036;PMID:32822427	PCS		40/60			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-24];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0003326	PMID:32822427	PCS		8/10			P	HPO:probinson[2020-08-24];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0003565	PMID:32822427	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0410246	PMID:8190036;PMID:32822427	PCS		53/60			P	HPO:probinson[2020-10-02];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0002014	PMID:8190036	PCS		41/50			P	HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0002013	PMID:8190036;PMID:32822427	PCS		31/60			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-24];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0000155	PMID:32822427	PCS		6/10			P	HPO:probinson[2020-08-24];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0002373	PMID:32822427	PCS		2/10			P	HPO:probinson[2020-08-24];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0003261	PMID:32822427;PMID:21708801	PCS		26/40			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-24];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0009098	PMID:32822427	PCS		2/10			P	HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0002829	PMID:21708801	PCS		33/50			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0000007	PMID:32822427	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0001954	PMID:8190036	PCS		50/50			P	HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0000988	PMID:32822427;PMID:16435210	PCS		20/20			P	HPO:probinson[2020-08-24];HPO:probinson[2020-08-24];HPO:skoehler[2009-02-17];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0000543	PMID:16435210	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0001433	PMID:32822427	PCS		10/10			P	HPO:probinson[2020-08-24];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0002027	PMID:8190036;PMID:32822427;PMID:21708801	PCS		74/110			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-24];HPO:probinson[2020-10-02];HPO:probinson[2020-08-24]
OMIM:260920	Hyper-Igd syndrome		HP:0001974	PMID:8190036	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2020-10-02]
OMIM:260920	Hyper-Igd syndrome		HP:0002028	PMID:32822427;PMID:21708801	PCS		44/60			P	HPO:probinson[2020-08-24];HPO:probinson[2020-08-24];HPO:probinson[2020-08-24]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0000252	OMIM:615190	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0004313	OMIM:615190	TAS					P	HPO:skoehler[2015-09-11]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0001321	OMIM:615190	TAS		HP:0040281			P	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0001882	OMIM:615190	TAS					P	HPO:skoehler[2015-09-11]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0002583	OMIM:615190	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0001263	OMIM:615190	TAS		HP:0040281			P	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0010450	OMIM:615190	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0003828	OMIM:615190	TAS					M	HPO:skoehler[2015-12-30]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0000007	OMIM:615190	TAS					I	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0008897	OMIM:615190	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0001511	OMIM:615190	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0005528	OMIM:615190	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0008404	OMIM:615190	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0000006	OMIM:615190	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615190	Dyskeratosis congenita, autosomal recessive 5		HP:0002721	OMIM:615190	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0003236	PMID:16793013	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0003596	PMID:16793013;PMID:16483541	PCS		2/2			C	HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0000518	PMID:16793013	PCS		0/1			P	HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0001653	PMID:16793013	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0033755	PMID:16793013	IEA		1/1			P	HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0012665	PMID:16793013	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0000006	PMID:16483541	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0004756	PMID:16483541	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:615184	Cardiomyopathy, dilated, 1II		HP:0001644	PMID:16793013;PMID:16483541	PCS		2/2		HP:0012825	P	HPO:probinson[2022-07-04];HPO:skoehler[2013-06-06];HPO:probinson[2022-07-04]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0000750	PMID:35718349	PCS		1/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0000486	PMID:35718349	PCS		1/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0003487	PMID:35718349	PCS		5/5			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0001332	PMID:35718349	PCS		0/5			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0002395	PMID:35718349	PCS		7/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0001260	PMID:35718349	PCS		0/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0003593	PMID:35718349	PCS		5/7			C	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0002064	PMID:35718349	PCS		7/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0002061	PMID:35718349	PCS		7/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0002194	PMID:35718349	PCS		7/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0000639	PMID:35718349	PCS		1/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0007350	PMID:35718349	PCS		0/5			P	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0011463	PMID:35718349	PCS		2/7			C	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0002938	PMID:35718349	PCS		4/7			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0000007	PMID:35718349	PCS					I	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0006986	PMID:35718349	PCS		0/5			P	HPO:probinson[2022-08-20]
OMIM:619966	Spastic paraplegia 87, autosomal recessive		HP:0001347	PMID:35718349	PCS		7/7			P	HPO:probinson[2022-08-20]
OMIM:185900	Chromosome 2q35 duplication syndrome		HP:0011939	PMID:21167467	PCS					P	HPO:probinson[2024-07-22]
OMIM:185900	Chromosome 2q35 duplication syndrome		HP:0003577	PMID:21167467	PCS					C	HPO:probinson[2024-07-22]
OMIM:185900	Chromosome 2q35 duplication syndrome		HP:0004442	PMID:21167467	PCS		HP:0040283			P	HPO:skoehler[2013-09-30];HPO:probinson[2024-07-22]
OMIM:185900	Chromosome 2q35 duplication syndrome		HP:0004691	PMID:21167467	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-07-22]
OMIM:185900	Chromosome 2q35 duplication syndrome		HP:0000006	PMID:21167467	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-07-22]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0030843	PMID:22693999	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0001278	PMID:22693999	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0000969	PMID:22693999	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0100292	PMID:22693999	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0001271	PMID:22693999	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0012450	PMID:22693999	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0002094	PMID:22693999	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0012280	PMID:22693999	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0001824	PMID:22693999	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0000006	PMID:22693999	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620659	Amyloidosis, hereditary systemic 6		HP:0002028	PMID:22693999	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:177200	Liddle syndrome 1		HP:0003621	PMID:8524790	PCS		1/3			C	HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0000083	PMID:8524790	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0011463	PMID:8524790	PCS		2/3			C	HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0001949	PMID:8524790	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0003351	PMID:8524790	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0000822	PMID:8524790	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0002900	PMID:8524790	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0004319	PMID:8524790	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:177200	Liddle syndrome 1		HP:0000006	PMID:8524790	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0001297	PMID:24827035	PCS		3/27			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0002155	PMID:24827035	PCS		5/27			P	HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0003596	PMID:24827035	PCS		22/27			C	HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0003124	PMID:24827035	PCS		11/27			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0005145	PMID:24827035	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0003141	PMID:24827035	PCS		10/27			P	HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0003074	PMID:24827035	PCS		5/27			P	HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0012743	PMID:24827035	PCS		26/26			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0011462	PMID:24827035	PCS		5/27			C	HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0000822	PMID:24827035	PCS		27/27		HP:0012828	P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0001658	PMID:24827035	PCS		23/27			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0001956	PMID:24827035	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0005978	PMID:24827035	PCS		25/27			P	HPO:probinson[2023-01-19]
OMIM:615812	Abdominal obesity-metabolic syndrome 3		HP:0000006	PMID:24827035	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-19]
OMIM:173700	Poikiloderma, hereditary sclerosing		HP:0007618	OMIM:173700	TAS					P	HPO:iea[2009-02-17]
OMIM:173700	Poikiloderma, hereditary sclerosing		HP:0100759	OMIM:173700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:173700	Poikiloderma, hereditary sclerosing		HP:0001217	OMIM:173700	TAS					P	HPO:iea[2009-02-17]
OMIM:173700	Poikiloderma, hereditary sclerosing		HP:0000006	OMIM:173700	TAS					I	HPO:iea[2009-02-17]
OMIM:173700	Poikiloderma, hereditary sclerosing		HP:0001029	OMIM:173700	TAS					P	HPO:iea[2012-07-20]
OMIM:309000	Lowe syndrome		HP:0003236	PMID:27011217	PCS	HP:0003577				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0003355	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0004322	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001250	PMID:27011217	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0100490	OMIM:309000	TAS					P	HPO:probinson[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0000083	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001252	PMID:27011217	PCS	HP:0003577				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0000718	OMIM:309000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:309000	Lowe syndrome		HP:0000519	PMID:27011217	PCS	HP:0030674				P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0004639	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0003109	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0008897	PMID:27011217	PCS	HP:0003593				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0002857	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0000559	PMID:27011217	PCS	HP:0011463				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0002019	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001249	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0007109	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0003126	PMID:27011217	PCS	HP:0003577				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0025131	OMIM:309000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309000	Lowe syndrome		HP:0007948	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0003124	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001382	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001263	PMID:27011217	PCS	HP:0003593				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0010562	PMID:27011217	PCS	HP:0011463				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0001419	OMIM:309000	IEA					I	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0002827	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0000926	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0002748	OMIM:309000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:309000	Lowe syndrome		HP:0000568	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0002749	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0003774	PMID:27011217	PCS	HP:0003581				P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0003577	PMID:27011217	PCS					C	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0011432	PMID:27011217	PCS	HP:0030674				H	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:6000615	PMID:20301653	PCS					P	HPO:probinson[2024-04-03]
OMIM:309000	Lowe syndrome		HP:0001508	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0006297	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0000733	OMIM:309000	IEA	HP:0030674				P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0007663	OMIM:309000	TAS					P	HPO:skoehler[2015-07-26]
OMIM:309000	Lowe syndrome		HP:0002119	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0025435	PMID:27011217	PCS					P	HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0003646	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001225	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0002756	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0003148	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0002650	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001284	PMID:27011217	PCS	HP:0003577				P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0001482	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0009473	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0002808	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001319	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0000505	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0001994	PMID:27011217	PCS	HP:0003593				P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:309000	Lowe syndrome		HP:0000028	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0000501	OMIM:309000	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:309000	Lowe syndrome		HP:0002049	OMIM:309000	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002069	PMID:11181577	PCS		1/1			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001254	PMID:10944442	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002421	OMIM:252010	IEA					P	HPO:skoehler[2019-02-22]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000486	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001252	PMID:11181577;PMID:10944442	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001251	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003593	PMID:10944442	PCS		2/2			C	HPO:skoehler[2019-02-22];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0004481	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002181	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000639	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001522	PMID:10944442	PCS		2/2			C	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001324	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002415	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0007965	PMID:10944442	PCS		2/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003546	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003348	PMID:10944442	PCS		2/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001265	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003202	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000252	PMID:10944442	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003200	PMID:11181577;PMID:10944442	PCS		1/3			P	HPO:probinson[2021-08-18];HPO:probinson[2021-08-18];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003487	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000331	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0011924	PMID:10944442	PCS		2/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002352	OMIM:252010	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001263	PMID:11181577	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0011923	PMID:11181577;PMID:10944442	PCS		3/3			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0100660	OMIM:252010	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0008160	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000407	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000007	OMIM:252010	IEA					I	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000961	PMID:11181577	PCS		1/1			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000047	PMID:10944442	PCS		1/1	MALE		P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001257	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002104	PMID:11181577	PCS		1/1			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001259	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001138	OMIM:252010	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000582	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001399	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001272	OMIM:252010	TAS					P	HPO:skoehler[2012-10-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0005157	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002240	PMID:10944442	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0032653	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0007183	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001508	PMID:11181577;PMID:10944442	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000817	PMID:10944442	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000618	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001427	OMIM:252010	IEA					I	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0008872	PMID:10944442	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001943	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003648	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002878	PMID:10944442	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001308	PMID:11181577	PCS		1/1			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001744	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001347	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0003128	PMID:10944442	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002376	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002013	PMID:11181577	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002490	PMID:10944442	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002093	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0012752	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001639	PMID:11181577	PCS		1/1			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0012240	PMID:11181577;PMID:10944442	PCS		2/3			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000508	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0002922	PMID:10944442	PCS		1/2			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0000543	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0001510	OMIM:252010	TAS					P	HPO:skoehler[2012-10-17]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0004900	PMID:11181577	PCS		1/1			P	HPO:probinson[2021-08-18]
OMIM:252010	Mitochondrial complex I deficiency, nuclear type 1		HP:0006965	OMIM:252010	IEA					P	HPO:iea[2009-02-17]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0003676	PMID:28503735	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0002540	PMID:28503735	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0001250	PMID:28503735	PCS		5/6			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0030674	PMID:28503735	PCS		1/6			C	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0001252	PMID:28503735	PCS		3/6			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0003593	PMID:28503735	PCS		3/6			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0011167	PMID:28503735	PCS		1/6			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0002119	PMID:28503735	PCS		7/11			P	HPO:probinson[2022-10-30];HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0006872	PMID:28503735	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0003623	PMID:28503735	PCS		2/6			C	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0002751	PMID:28503735	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0008936	PMID:28503735	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0002510	PMID:28503735	PCS		5/6			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0000252	PMID:28503735	PCS		4/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0001344	PMID:28503735	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0002079	PMID:28503735	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0002098	PMID:28503735	PCS		1/6			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0001263	PMID:28503735	PCS		9/12			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0034392	PMID:28503735	PCS		5/6			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0034295	PMID:28503735	PCS		5/5			P	HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0000007	PMID:28503735	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0000505	PMID:28503735	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0001258	PMID:28503735	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617977	Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures		HP:0001257	PMID:28503735	PCS		1/6			P	HPO:probinson[2022-10-30]
OMIM:620103	Spermatogenic failure 77		HP:0034309	PMID:36150389	PCS		3/4			P	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0030345	PMID:36150389	PCS		0/6			P	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0011462	PMID:36150389	PCS		6/6			C	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0003251	PMID:36150389	PCS		6/6			P	HPO:probinson[2022-11-24];HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0008232	PMID:36150389	PCS		6/6			P	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0030087	PMID:36150389	PCS		0/6			P	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0000007	PMID:36150389	PCS					I	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0000798	PMID:36150389	PCS		5/6			P	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0000028	PMID:36150389	PCS		2/6			P	HPO:probinson[2022-11-24]
OMIM:620103	Spermatogenic failure 77		HP:0000027	PMID:36150389	PCS		1/6			P	HPO:probinson[2022-11-24]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0011904	PMID:15977037	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0002240	PMID:15977037	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0045048	PMID:15977037	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0025547	PMID:15977037	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0001935	PMID:15977037	PCS		1/1		HP:0012825	P	HPO:probinson[2021-10-22]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0000006	PMID:15977037	PCS					I	HPO:probinson[2021-10-22];HPO:probinson[2021-10-22]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0001744	PMID:15977037	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:603902	Thalassemia-beta, dominant inclusion-body		HP:0020080	PMID:15977037	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:240400	HYPOASCORBEMIA		HP:0001939	OMIM:240400	IEA					P	HPO:iea[2009-02-17]
OMIM:240400	HYPOASCORBEMIA		HP:0000007	OMIM:240400	IEA					I	HPO:iea[2009-02-17]
OMIM:132990	Erythema nodosum, familial		HP:0012219	OMIM:132990	IEA					P	HPO:skoehler[2015-01-27]
OMIM:132990	Erythema nodosum, familial		HP:0010783	OMIM:132990	IEA					P	HPO:skoehler[2010-06-20]
OMIM:132990	Erythema nodosum, familial		HP:0000006	OMIM:132990	IEA					I	HPO:iea[2009-02-17]
OMIM:300030	Deafness, X-linked 3		HP:0001419	OMIM:300030	TAS				HP:0012828	I	HPO:probinson[2012-07-16]
OMIM:300030	Deafness, X-linked 3		HP:0008527	OMIM:300030	TAS				HP:0012828	P	HPO:probinson[2009-02-17]
OMIM:128710	Ear pits, posterior helical		HP:0008523	OMIM:128710	TAS					P	HPO:probinson[2009-02-17]
OMIM:128710	Ear pits, posterior helical		HP:0000006	OMIM:128710	TAS					I	HPO:probinson[2009-02-17]
OMIM:244100	Jumping frenchman of maine		HP:0000707	OMIM:244100	IEA					P	HPO:iea[2009-02-17]
OMIM:244100	Jumping frenchman of maine		HP:0000007	OMIM:244100	IEA					I	HPO:iea[2009-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0001332	PMID:12742592	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0002079	OMIM:613720	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0001250	PMID:12742592	PCS		1/1			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0001263	PMID:12742592	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0001285	OMIM:613720	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0001252	PMID:12742592	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0003593	OMIM:613720	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0010851	PMID:12742592	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0200134	PMID:12742592	PCS		1/1			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0000006	PMID:12742592	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0001249	OMIM:613720	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613720	Epileptic encephalopathy, early infantile, 7		HP:0003623	PMID:12742592	PCS		1/1			C	HPO:probinson[2023-02-17]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001276	PMID:23768512	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0002421	PMID:23768512	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0003577	PMID:23768512	PCS		1/4			C	HPO:probinson[2022-11-05];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0003236	PMID:23768512	PCS		4/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0000486	PMID:23768512	PCS		3/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001250	PMID:23768512	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001252	PMID:23768512	PCS		2/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0003593	PMID:23768512	PCS		2/4			C	HPO:probinson[2022-11-05];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001270	PMID:23768512	PCS		2/8			P	HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0000518	PMID:23768512	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0000639	PMID:23768512	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001324	PMID:23768512	PCS		4/4		HP:0012828	P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001249	PMID:23768512	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0003623	PMID:23768512	PCS		1/4			C	HPO:probinson[2022-11-05];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0002058	PMID:23768512	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0000252	PMID:23768512	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001321	PMID:23768512	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0011968	PMID:23768512	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0030046	PMID:23768512	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001263	PMID:23768512	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0003560	PMID:23768512	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0011102	PMID:23768512	PCS		1/4			P	HPO:probinson[2022-11-05];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0034392	PMID:23768512	PCS					P	HPO:probinson[2022-11-05];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0009055	PMID:23768512	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0000508	PMID:23768512	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0000007	PMID:23768512	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001558	PMID:23768512	PCS		3/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:615351	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 14		HP:0001657	PMID:23768512	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-05]
OMIM:114200	Camptodactyly 1		HP:0100490	OMIM:114200	TAS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2013-08-10]
OMIM:114200	Camptodactyly 1		HP:0003166	OMIM:114200	TAS					P	HPO:probinson[2013-08-10]
OMIM:114200	Camptodactyly 1		HP:0032153	OMIM:114200	IEA					P	HPO:skoehler[2019-09-07]
OMIM:114200	Camptodactyly 1		HP:0000006	OMIM:114200	IEA					I	HPO:iea[2009-02-17]
OMIM:114200	Camptodactyly 1		HP:0004976	OMIM:114200	IEA					P	HPO:iea[2013-08-10]
OMIM:190100	Geniospasm 1		HP:0012462	OMIM:190100	TAS					P	HPO:skoehler[2013-11-28]
OMIM:190100	Geniospasm 1		HP:0000739	OMIM:190100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:190100	Geniospasm 1		HP:0000006	OMIM:190100	TAS					I	HPO:skoehler[2009-02-17]
OMIM:618113	Encephalitis/encephalopathy, mild, with reversible myelin vacuolization		HP:0003621	PMID:29265453	PCS		6/9			C	HPO:probinson[2022-12-21]
OMIM:618113	Encephalitis/encephalopathy, mild, with reversible myelin vacuolization		HP:0006846	PMID:29265453	PCS		9/9			P	HPO:probinson[2022-12-21]
OMIM:618113	Encephalitis/encephalopathy, mild, with reversible myelin vacuolization		HP:0001250	PMID:29265453	PCS		9/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-21]
OMIM:618113	Encephalitis/encephalopathy, mild, with reversible myelin vacuolization		HP:0011463	PMID:29265453	PCS		3/9			C	HPO:probinson[2022-12-21]
OMIM:618113	Encephalitis/encephalopathy, mild, with reversible myelin vacuolization		HP:0000006	PMID:29265453	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000286	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001055	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000684	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001773	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001530	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001250	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000160	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0004440	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000086	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000085	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0003073	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000319	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0011065	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000316	PMID:19935664	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000752	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001004	PMID:19935664	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000278	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001007	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001249	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000677	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002750	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002035	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002593	PMID:19935664	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001263	PMID:19935664	PCS		1/7			P	HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0010554	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002194	PMID:19935664	PCS		1/7			P	HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0005183	OMIM:235510	TAS					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0012385	OMIM:235510	TAS					P	HPO:skoehler[2013-10-22]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0100539	OMIM:235510	TAS					P	HPO:skoehler[2012-10-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000407	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000767	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001537	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000007	PMID:19935664	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0007598	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000405	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001698	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002866	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000369	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000126	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002202	OMIM:235510	TAS					P	HPO:probinson[2012-05-01]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000189	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002243	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0003298	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001790	PMID:19935664	PCS		1/7			P	HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0012368	PMID:19935664	PCS		7/7			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001629	PMID:19935664	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000337	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0006531	PMID:19935664	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001302	OMIM:235510	IEA					P	HPO:skoehler[2010-06-20]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000212	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000076	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000431	OMIM:235510	TAS					P	HPO:probinson[2012-05-01]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0002650	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0004279	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001762	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000272	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0005280	PMID:19935664	PCS		7/7			P	HPO:probinson[2012-05-01]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0009473	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0006521	PMID:19935664	PCS		6/7			P	HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0200055	OMIM:235510	TAS					P	HPO:skoehler[2012-10-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0001631	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000028	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0000501	PMID:19935664	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:235510	Hennekam lymphangiectasia-lymphedema syndrome		HP:0008229	OMIM:235510	IEA					P	HPO:iea[2009-02-17]
OMIM:617234	Preimplantation embryonic lethality 2		HP:0000789	OMIM:617234	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617234	Preimplantation embryonic lethality 2		HP:0000007	PMID:27545678	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-04-20]
OMIM:617234	Preimplantation embryonic lethality 2		HP:0032479	PMID:27545678	PCS					P	HPO:probinson[2019-04-20]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0004322	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0002750	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0000958	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0001609	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0000821	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0000007	OMIM:275120	TAS					I	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0008237	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0001324	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0002019	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:275120	Thyrotropin-Releasing hormone deficiency		HP:0001249	OMIM:275120	TAS					P	HPO:probinson[2012-04-11]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0000230	PMID:27291868	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0002684	PMID:27291868	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0002240	PMID:27291868	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0012378	PMID:27291868	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0006480	PMID:27291868	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0001903	PMID:27291868	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0011463	PMID:17997709	PCS		1/1			C	HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0000938	PMID:17997709	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0000843	PMID:27291868	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0002757	PMID:27291868	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0000768	PMID:27291868	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0000006	PMID:17997709	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0001744	PMID:27291868	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-08]
OMIM:618107	Osteopetrosis, autosomal dominant 3		HP:0025406	PMID:27291868	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000286	PMID:26924530	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000365	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0004322	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0003196	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0410030	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0010297	PMID:26924530	PCS		3/3			P	HPO:probinson[2021-01-09]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000316	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0001643	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000175	PMID:26924530	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000054	PMID:26924530	PCS		1/1	MALE		P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0011800	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0010954	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0005180	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0012385	PMID:26924530	PCS		1/4			P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000689	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000527	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0001539	PMID:26924530	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000207	PMID:26924530	PCS		1/4			P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000520	PMID:26924530	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000960	PMID:26924530	PCS		1/4			P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000006	PMID:26924530	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000369	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0006349	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0001655	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000582	PMID:26924530	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000343	PMID:26924530	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000463	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0001156	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000060	PMID:26924530	PCS		1/3	FEMALE		P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0001629	PMID:26924530	PCS	HP:0003577	2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0030084	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0002714	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0004935	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000212	PMID:26924530	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000256	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0009803	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0001545	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0003027	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000076	PMID:26924530	PCS		1/4			P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0002650	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000431	PMID:26924530	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000592	PMID:26924530	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000470	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0005280	PMID:26924530	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0011304	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0002808	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000506	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000348	PMID:26924530	PCS		1/4			P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0002007	PMID:26924530	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0001159	PMID:26924530	PCS		1/4			P	HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000465	PMID:26924530	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000028	PMID:26924530	PCS		1/1	MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:616894	Robinow syndrome, autosomal dominant 3		HP:0000347	PMID:26924530	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-03]
OMIM:223400	Duodenal atresia		HP:0000007	OMIM:223400	IEA					I	HPO:iea[2009-02-17]
OMIM:223400	Duodenal atresia		HP:0002247	OMIM:223400	IEA					P	HPO:iea[2009-02-17]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0001892	PMID:12664304	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0000132	PMID:12664304	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0001022	PMID:12664304	PCS		7/7			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0002091	PMID:12664304	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0033263	PMID:12664304	PCS		7/7			P	HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0007750	OMIM:614073	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0000007	PMID:12664304	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0001107	OMIM:614073	IEA					P	HPO:probinson[2013-08-10]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0007663	PMID:12664304	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0000978	PMID:12664304	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0002206	PMID:12664304	PCS		1/7			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0000421	PMID:12664304	PCS		5/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:614073	Hermansky-Pudlak syndrome 4		HP:0000666	OMIM:614073	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003236	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0030234	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001252	OMIM:251900	IEA					P	HPO:iea[2009-02-17]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003394	OMIM:251900	IEA		1/1			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0002240	OMIM:251900	IEA					P	HPO:iea[2009-02-17]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001290	OMIM:251900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001270	OMIM:251900	IEA					P	HPO:iea[2009-02-17]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003391	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0002919	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0000639	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0007141	OMIM:251900	IEA					P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0007340	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001427	OMIM:251900	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0002913	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0008314	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0002515	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0000158	OMIM:251900	IEA					P	HPO:iea[2009-02-17]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001324	OMIM:251900	IEA					P	HPO:iea[2009-02-17]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003701	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003325	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001347	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003128	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003326	OMIM:251900	IEA		1/1			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001265	OMIM:251900	IEA					P	HPO:iea[2009-02-17]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003621	PMID:24281368	PCS		1/1			C	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001288	OMIM:251900	IEA					P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001761	OMIM:251900	IEA					P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003201	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0002151	PMID:24281368	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0002094	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0000508	OMIM:251900	IEA					P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0000007	PMID:24281368	PCS					I	HPO:nvasilevsky[2019-03-11];HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0000821	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001935	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0000648	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0000505	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003737	OMIM:251900	IEA					P	HPO:iea[2009-02-17]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001257	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0003535	PMID:24281368	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:251900	Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy		HP:0001875	OMIM:251900	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001531	PMID:30824121	PCS		2/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002188	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001332	PMID:30824121	PCS		1/4		HP:0012825	P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0004322	PMID:30824121	PCS		2/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001250	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001371	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0004684	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001252	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000041	PMID:30824121	PCS					P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000716	PMID:30824121	PCS		1/4		HP:0012825	P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002616	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002311	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000176	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000252	PMID:30824121	PCS		2/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002079	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001260	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000490	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002075	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002194	PMID:30824121	PCS		4/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0011448	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0009055	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000007	PMID:30824121	PCS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000722	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0005978	PMID:30824121	PCS		2/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000047	PMID:30824121	PCS					P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000341	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001272	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000460	PMID:30824121	PCS		2/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0010862	PMID:30824121	PCS		4/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0008070	PMID:30824121	PCS					P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000737	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0008872	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001348	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002059	PMID:30824121	PCS	HP:0011462	1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002136	PMID:30824121	PCS		2/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002213	PMID:30824121	PCS		3/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000750	PMID:30824121	PCS		4/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002133	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001761	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0002299	PMID:30824121	PCS					P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001518	PMID:30824121	PCS	HP:0003577	1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0012043	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0007256	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000348	PMID:30824121	IEA		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0000823	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001511	PMID:30824121	PCS	HP:0030674	2/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0007018	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618891	Microcephaly, developmental delay, and brittle hair syndrome		HP:0001631	PMID:30824121	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:619557	SIMHA syndrome		HP:0000286	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000387	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000365	PMID:24907849	PCS		0/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0001212	PMID:24907849	PCS		1/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000486	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0004322	PMID:24907849	PCS		1/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0001252	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0003593	PMID:24907849	PCS		2/2			C	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0001845	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0030043	PMID:24907849	PCS		1/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000219	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0002714	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000411	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0001488	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000750	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0002650	PMID:24907849	PCS		0/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0031936	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0025335	PMID:24907849	PCS		1/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0001263	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0011800	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0002808	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000007	PMID:24907849	PCS					I	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0005617	PMID:24907849	PCS		1/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0000664	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0001510	PMID:24907849	PCS		2/2			P	HPO:probinson[2022-01-23]
OMIM:619557	SIMHA syndrome		HP:0004689	PMID:24907849	PCS		1/2			P	HPO:probinson[2022-01-23]
OMIM:301845	Bazex syndrome		HP:0001056	OMIM:301845	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301845	Bazex syndrome		HP:0003764	OMIM:301845	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301845	Bazex syndrome		HP:0001047	OMIM:301845	IEA					P	HPO:skoehler[2010-06-18]
OMIM:301845	Bazex syndrome		HP:0000430	OMIM:301845	IEA					P	HPO:iea[2009-02-17]
OMIM:301845	Bazex syndrome		HP:0000221	OMIM:301845	TAS					P	HPO:probinson[2022-09-11]
OMIM:301845	Bazex syndrome		HP:0001382	OMIM:301845	IEA					P	HPO:iea[2009-02-17]
OMIM:301845	Bazex syndrome		HP:0002671	OMIM:301845	IEA					P	HPO:iea[2009-02-17]
OMIM:301845	Bazex syndrome		HP:0025367	OMIM:301845	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:301845	Bazex syndrome		HP:0003593	OMIM:301845	IEA					C	HPO:iea[2009-02-17]
OMIM:301845	Bazex syndrome		HP:0008070	OMIM:301845	IEA					P	HPO:iea[2009-02-17]
OMIM:301845	Bazex syndrome		HP:0040154	OMIM:301845	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:301845	Bazex syndrome		HP:0032152	OMIM:301845	IEA					P	HPO:skoehler[2019-02-22]
OMIM:301845	Bazex syndrome		HP:0000418	OMIM:301845	IEA					P	HPO:iea[2009-02-17]
OMIM:301845	Bazex syndrome		HP:0000953	OMIM:301845	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301845	Bazex syndrome		HP:0000964	OMIM:301845	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:301845	Bazex syndrome		HP:0000966	OMIM:301845	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301845	Bazex syndrome		HP:0002208	OMIM:301845	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301845	Bazex syndrome		HP:0009886	OMIM:301845	IEA					P	HPO:skoehler[2010-06-18]
OMIM:301845	Bazex syndrome		HP:0009765	OMIM:301845	TAS					P	HPO:skoehler[2017-07-13]
OMIM:301845	Bazex syndrome		HP:0001423	OMIM:301845	IEA					I	HPO:iea[2009-02-17]
OMIM:301845	Bazex syndrome		HP:0003777	OMIM:301845	IEA					P	HPO:iea[2009-02-17]
OMIM:612370	Hypogonadotropic hypogonadism 5 with or without anosmia		HP:0000044	PMID:18834967	PCS					P	HPO:probinson[2013-02-19]
OMIM:612370	Hypogonadotropic hypogonadism 5 with or without anosmia		HP:0000175	OMIM:612370	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612370	Hypogonadotropic hypogonadism 5 with or without anosmia		HP:0000407	OMIM:612370	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612370	Hypogonadotropic hypogonadism 5 with or without anosmia		HP:0000458	PMID:18834967	PCS		HP:0040282			P	HPO:probinson[2013-02-19]
OMIM:612370	Hypogonadotropic hypogonadism 5 with or without anosmia		HP:0410030	OMIM:612370	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612370	Hypogonadotropic hypogonadism 5 with or without anosmia		HP:0000006	PMID:18834967	PCS					I	HPO:probinson[2013-01-09]
OMIM:612370	Hypogonadotropic hypogonadism 5 with or without anosmia		HP:0000028	OMIM:612370	TAS					P	HPO:skoehler[2017-07-13]
OMIM:145701	Hypertrichosis universalis congenita, Ambras type		HP:0004540	OMIM:145701	TAS					P	HPO:skoehler[2015-01-21]
OMIM:145701	Hypertrichosis universalis congenita, Ambras type		HP:0000006	OMIM:145701	IEA					I	HPO:iea[2009-02-17]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000220	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000582	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000343	PMID:31334757;PMID:22633399;PMID:32696056	PCS		4/6			P	HPO:probinson[2021-10-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0001156	PMID:22633399	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0004322	OMIM:614701	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000463	PMID:31334757;PMID:22633399	PCS		2/5			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000381	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0001250	PMID:31334757	PCS		1/3			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0003196	PMID:31334757	PCS		1/3			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002020	PMID:31334757;PMID:22633399	PCS		2/5			P	HPO:probinson[2021-10-19];HPO:skoehler[2012-11-18];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0033785	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0012368	PMID:32696056	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0100864	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000319	PMID:22633399;PMID:32696056	PCS		2/3			P	HPO:probinson[2021-10-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002937	OMIM:614701	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0011461	PMID:32696056	PCS		1/1			C	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000954	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000316	PMID:31334757	PCS		1/3			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0006870	PMID:32696056	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000219	PMID:22633399	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002812	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002119	PMID:32696056	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002678	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0001488	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002974	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002553	PMID:22633399	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000176	PMID:31334757;PMID:22633399	PCS		2/5			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000175	OMIM:614701	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000252	PMID:31334757;PMID:22633399	PCS		4/4			P	HPO:probinson[2021-10-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000574	PMID:31334757;PMID:22633399	PCS		3/5			P	HPO:skoehler[2013-01-22];HPO:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000431	PMID:22633399;PMID:32696056	PCS		3/3			P	HPO:probinson[2021-10-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000233	PMID:31334757;PMID:32696056	PCS		2/4			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0001263	PMID:31334757;PMID:22633399	PCS		5/5			P	HPO:skoehler[2013-01-22];HPO:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0004691	PMID:22633399	PCS		2/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0100777	OMIM:614701	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000965	PMID:22633399	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0001636	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000601	PMID:31334757;PMID:32696056	PCS		2/4			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0004209	PMID:31334757;PMID:22633399	PCS		2/5			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000768	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0001159	OMIM:614701	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000664	PMID:31334757;PMID:22633399	PCS		3/5			P	HPO:probinson[2021-10-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000006	PMID:22633399	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0008428	PMID:22633399	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0002566	PMID:22633399	PCS		1/2			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000248	PMID:31334757	PCS		1/3			P	HPO:probinson[2021-10-19]
OMIM:614701	Cornelia de Lange syndrome 4		HP:0000369	PMID:31334757	PCS		1/3			P	HPO:probinson[2021-10-19]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001650	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000483	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0004322	PMID:12525539;PMID:23897642	PCS		11/11			P	HPO:probinson[2021-05-27];HPO:probinson[2021-05-26]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0010049	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0100693	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0009381	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0011222	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000518	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0002938	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0003508	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001643	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001642	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001169	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000692	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001387	PMID:12525539	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-26]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0002750	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001783	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001065	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0012019	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0011003	PMID:12525539;PMID:23897642	PCS		11/11			P	HPO:probinson[2021-05-27];HPO:iea[2009-02-17];HPO:probinson[2021-05-26]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001537	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000327	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001538	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001653	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0002987	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000248	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000006	PMID:12525539	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-26]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000885	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000189	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0005830	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001156	PMID:12525539	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-26]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0002682	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001230	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001072	OMIM:608328	IEA					P	HPO:skoehler[2019-04-18]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0010743	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001629	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000618	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000218	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0009768	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0004933	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0002753	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000594	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0002650	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0030961	PMID:12525539	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-26]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000391	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001083	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0005280	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0006482	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0100679	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0001635	PMID:23897642	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0003416	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000586	OMIM:608328	IEA					P	HPO:iea[2009-02-17]
OMIM:608328	Weill-Marchesani syndrome 2, dominant		HP:0000501	PMID:12525539	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-26]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0002465	PMID:25125150	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000286	PMID:25125150	PCS		1/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000486	PMID:25125150	PCS		2/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0004322	PMID:25125150	PCS		4/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001250	PMID:25125150	PCS		5/8			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001252	PMID:25125150	PCS		5/8			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001251	PMID:25125150	PCS		1/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0003593	PMID:25125150	PCS		1/8			C	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0010862	PMID:25125150	PCS		5/5			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000639	PMID:25125150	PCS		1/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0011463	PMID:25125150	PCS		7/8			C	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000718	PMID:25125150	PCS		5/8			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0002119	PMID:25125150	PCS		1/5			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000713	PMID:25125150	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000411	PMID:25125150	PCS		1/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001763	PMID:25125150	PCS		2/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001249	PMID:25125150	PCS		8/8			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001520	PMID:25125150	PCS		3/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000750	PMID:25125150	PCS		8/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001263	PMID:25125150	PCS		8/8			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0002194	PMID:25125150	PCS		8/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000007	PMID:25125150	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0100716	PMID:25125150	PCS		3/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000664	PMID:25125150	PCS		1/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0001510	PMID:25125150	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000303	PMID:25125150	PCS		1/8			P	HPO:probinson[2022-06-15]
OMIM:616116	Intellectual developmental disorder, autosomal recessive 46		HP:0000687	PMID:25125150	PCS		1/8			P	HPO:probinson[2022-06-15]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000483	PMID:32293671	PCS		1/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0001891	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0010804	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0003233	PMID:32293671	PCS		2/6			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0001773	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0004322	PMID:32293671	PCS		2/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0001250	PMID:32293671	PCS		6/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000020	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0001290	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0100785	PMID:32293671	PCS		6/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000639	PMID:32293671	PCS		1/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000817	PMID:32293671	PCS		5/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0012471	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0012153	PMID:32293671	PCS		2/6			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000316	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0025336	PMID:32293671	PCS	HP:0003593	3/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0002019	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000358	PMID:32293671	PCS		7/7			P	HPO:probinson[2023-02-06]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000494	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000252	PMID:32293671	PCS		2/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000750	PMID:32293671	PCS	HP:0003593				P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0031936	PMID:32293671	PCS	HP:0003593	5/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000276	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0031717	PMID:32293671	PCS		1/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0011968	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0001263	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0002194	PMID:32293671	PCS		5/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0012358	PMID:32293671	PCS		7/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0100512	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0012683	PMID:32293671	PCS		2/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0012101	PMID:32293671	PCS		6/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000729	PMID:32293671	PCS		6/7			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0031165	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000426	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000007	PMID:32293671	PCS					I	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000348	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000405	PMID:32293671	PCS		1/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0001852	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0200055	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000322	PMID:32293671	PCS					P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0002500	PMID:32293671	PCS		6/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000248	PMID:32293671	PCS		2/7			P	HPO:probinson[2020-06-23]
OMIM:618885	Congenital disorder of glycosylation, type IIt		HP:0000369	PMID:32293671	PCS		7/7			P	HPO:probinson[2023-02-06]
OMIM:619543	Boudin-Mortier syndrome		HP:0001166	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0000098	PMID:30032985	PCS		4/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0010639	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0001288	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0001382	PMID:30032985	PCS		3/4			P	HP:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0030771	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0000272	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0010511	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0032524	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0010264	PMID:30032985	PCS		4/4			P	HP:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0010275	PMID:30032985	PCS		4/4			P	HP:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0010022	PMID:30032985	PCS		4/4			P	HP:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0002616	PMID:30032985	PCS		2/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0000767	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0000007	PMID:30032985	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0100807	PMID:30032985	PCS		2/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0001847	PMID:30032985	PCS		2/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0030084	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0001763	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0001634	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:619543	Boudin-Mortier syndrome		HP:0000545	PMID:30032985	PCS		1/4			P	HP:probinson[2021-10-23]
OMIM:214290	Cervical vertebrae, agenesis of		HP:0000464	OMIM:214290	IEA					P	HPO:iea[2009-02-17]
OMIM:214290	Cervical vertebrae, agenesis of		HP:0000007	OMIM:214290	IEA					I	HPO:iea[2009-02-17]
OMIM:214290	Cervical vertebrae, agenesis of		HP:0008459	OMIM:214290	IEA					P	HPO:iea[2009-02-17]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0003477	PMID:21194679	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0003676	PMID:21194679	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0003401	PMID:21194679	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0001761	PMID:21194679	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0007460	PMID:21194679	PCS					P	HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0011462	PMID:21194679	PCS					C	HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0009830	PMID:21194679	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0002936	PMID:21194679	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0003409	PMID:21194679	PCS					P	HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0008404	PMID:21194679	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0000006	PMID:21194679	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0001347	PMID:21194679	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0002754	PMID:21194679	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-11-24]
OMIM:613708	Neuropathy, hereditary sensory, type ID		HP:0008944	PMID:21194679	PCS					P	HPO:probinson[2021-11-24]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001276	PMID:21620353	PCS	HP:0011463	3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0004322	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001371	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001252	PMID:21620353	PCS		3/3			P	HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000280	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0100962	PMID:21620353	PCS		3/3			P	HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0012471	OMIM:614067	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000316	OMIM:614067	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000414	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000218	OMIM:614067	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001347	PMID:21620353	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0003623	PMID:21620353	PCS		3/3			C	HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0008936	OMIM:614067	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000297	OMIM:614067	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000154	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000252	PMID:21620353	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001762	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000431	OMIM:614067	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0003487	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0031936	PMID:21620353	PCS		3/3			P	HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0002373	OMIM:614067	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001263	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0100021	OMIM:614067	IEA					P	HPO:skoehler[2015-01-21]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000448	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000007	PMID:21620353	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0002505	OMIM:614067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0002307	PMID:21620353	PCS		3/3			P	HPO:probinson[2023-06-09]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001258	OMIM:614067	IEA					P	HPO:skoehler[2015-01-21]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0007359	OMIM:614067	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0000322	OMIM:614067	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614067	Spastic paraplegia 52, autosomal recessive		HP:0001257	PMID:21620353	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:115650	Cataract, anterior polar, 1		HP:0001134	OMIM:115650	TAS					P	HPO:iea[2009-02-17]
OMIM:115650	Cataract, anterior polar, 1		HP:0000006	OMIM:115650	TAS					I	HPO:iea[2009-02-17]
OMIM:135580	Fibromuscular dysplasia of arteries		HP:0001297	OMIM:135580	TAS					P	HPO:iea[2009-02-17]
OMIM:135580	Fibromuscular dysplasia of arteries		HP:0005313	OMIM:135580	TAS					P	HPO:iea[2009-02-17]
OMIM:135580	Fibromuscular dysplasia of arteries		HP:0001658	OMIM:135580	TAS					P	HPO:iea[2009-02-17]
OMIM:135580	Fibromuscular dysplasia of arteries		HP:0100817	OMIM:135580	TAS					P	HPO:iea[2009-02-17]
OMIM:135580	Fibromuscular dysplasia of arteries		HP:0002647	OMIM:135580	TAS					P	HPO:iea[2009-02-17]
OMIM:135580	Fibromuscular dysplasia of arteries		HP:0004417	OMIM:135580	TAS					P	HPO:probinson[2013-03-12]
OMIM:135580	Fibromuscular dysplasia of arteries		HP:0000006	OMIM:135580	TAS					I	HPO:iea[2009-02-17]
OMIM:191550	Ureter, bifid or double		HP:0000073	OMIM:191550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:191550	Ureter, bifid or double		HP:0000006	OMIM:191550	IEA					I	HPO:iea[2009-02-17]
OMIM:612416	Factor XI deficiency		HP:0001892	OMIM:612416	TAS					P	HPO:probinson[2013-04-06]
OMIM:612416	Factor XI deficiency		HP:0001929	OMIM:612416	TAS					P	HPO:probinson[2013-04-06]
OMIM:612416	Factor XI deficiency		HP:0000007	OMIM:612416	TAS					I	HPO:probinson[2013-01-09]
OMIM:612416	Factor XI deficiency		HP:0000006	OMIM:612416	TAS					I	HPO:probinson[2013-04-06]
OMIM:612416	Factor XI deficiency		HP:0003645	OMIM:612416	TAS					P	HPO:probinson[2013-04-06]
OMIM:617585	Immunodeficiency 53		HP:0000010	PMID:26385063	PCS		1/3			P	HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0001508	PMID:26385063	PCS		1/3			P	HPO:skoehler[2019-04-18]
OMIM:617585	Immunodeficiency 53		HP:0002099	PMID:26385063	PCS		1/3			P	HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0003593	PMID:26385063	PCS		3/3			C	HPO:probinson[2023-05-19];HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0000007	PMID:26385063	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0000403	PMID:26385063	PCS		2/3			P	HPO:skoehler[2019-04-18]
OMIM:617585	Immunodeficiency 53		HP:0034315	PMID:26385063	PCS		3/3			P	HPO:probinson[2023-05-19];HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0006532	PMID:26385063	PCS		3/3			P	HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0000988	PMID:26385063	PCS		1/3			P	HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0002788	PMID:26385063	PCS		1/3			P	HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0003347	PMID:26385063	PCS		3/3			P	HPO:probinson[2023-05-19]
OMIM:617585	Immunodeficiency 53		HP:0011897	PMID:26385063	PCS		3/3			P	HPO:probinson[2023-05-19];HPO:probinson[2023-05-19]
OMIM:616843	Lymphedema, hereditary, III		HP:0000286	PMID:26333996	PCS		3/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0002202	PMID:26333996	PCS		1/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0000365	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0004322	PMID:26333996	PCS		1/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0000282	PMID:26333996	PCS					P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0002020	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0001790	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0031188	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0002619	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0000378	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0001004	PMID:26333996	PCS					P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0000377	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0001744	PMID:26333996	PCS		11/20			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0001561	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0002650	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0001541	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0000034	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0002593	PMID:26333996	PCS		1/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0001263	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0004392	PMID:26333996	PCS		1/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0010310	PMID:26333996	PCS		2/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0000969	PMID:26333996	PCS					P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0100539	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0100658	PMID:26333996	PCS		4/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0007430	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0000767	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0000007	PMID:26333996	PCS					I	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0000821	OMIM:616843	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616843	Lymphedema, hereditary, III		HP:0002625	PMID:26333996	PCS		1/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0001631	PMID:26333996	PCS		1/10			P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0000465	PMID:26333996	PCS					P	HPO:probinson[2017-06-23]
OMIM:616843	Lymphedema, hereditary, III		HP:0000347	PMID:26333996	PCS		1/10			P	HPO:probinson[2017-06-23]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000286	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0001762	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0002079	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0004322	PMID:4075567	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000243	PMID:4075567	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0012815	PMID:4075567	PCS		1/3			P	HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0001250	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0001040	PMID:4075567	PCS		1/3			P	HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000160	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000272	PMID:4075567	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0012368	OMIM:177980	TAS					P	HPO:skoehler[2013-10-22]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000308	PMID:4075567	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0011220	PMID:4075567	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000767	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0002007	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0002557	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0002536	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000377	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000047	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0001059	OMIM:177980	TAS					P	HPO:probinson[2012-07-22]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0000006	PMID:4075567	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:177980	Pterygia, impaired intellectual development, and distinctive craniofacial features		HP:0001249	OMIM:177980	IEA					P	HPO:iea[2009-02-17]
OMIM:169200	Pechet factor deficiency		HP:0001892	OMIM:169200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:169200	Pechet factor deficiency		HP:0000006	OMIM:169200	IEA					I	HPO:iea[2009-02-17]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0009804	PMID:18657636	PCS			MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0011051	PMID:16583127	PCS	HP:0003621	9/10	MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0002046	PMID:18657636	PCS		0/5	MALE		P	HPO:lccarmody[2018-06-13];HPO:probinson[2024-03-09]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0011947	PMID:18657636	PCS		0/5	MALE		P	HPO:lccarmody[2018-06-13];HPO:probinson[2024-03-09]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0001592	PMID:18657636	PCS			MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0011054	PMID:16583127	PCS		9/10	MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0000668	PMID:18657636	PCS		5/5	MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0001423	PMID:18657636	PCS					I	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0200153	PMID:18657636	PCS		5/5	MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0000674	PMID:18657636	PCS			MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0000677	PMID:18657636	PCS			MALE		P	HPO:lccarmody[2018-06-13]
OMIM:313500	Tooth agenesis, selective, X-linked, 1		HP:0010667	PMID:18657636	PCS		5/5	MALE		P	HPO:lccarmody[2018-06-13]
OMIM:124300	Darwinian point of pinna		HP:0011261	OMIM:124300	TAS					P	HPO:probinson[2022-08-26]
OMIM:124300	Darwinian tubercle of pinna		HP:0000006	OMIM:124300	TAS					I	HPO:iea[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0001014	OMIM:248510	TAS					P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0000365	OMIM:248510	TAS					P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0002167	OMIM:248510	TAS					P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0001250	OMIM:248510	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0001252	OMIM:248510	TAS					P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0003593	PMID:18565776	PCS		1/1			C	HPO:probinson[2022-07-01]
OMIM:248510	Mannosidosis, beta		HP:0001290	OMIM:248510	TAS					P	HPO:skoehler[2017-07-13]
OMIM:248510	Mannosidosis, beta		HP:0034367	PMID:18565776	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:248510	Mannosidosis, beta		HP:0012066	OMIM:248510	TAS					P	HPO:probinson[2012-08-04]
OMIM:248510	Mannosidosis, beta		HP:0002719	OMIM:248510	TAS					P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0000718	OMIM:248510	TAS					P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0001999	OMIM:248510	TAS		HP:0040283		HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0000503	OMIM:248510	TAS					P	HPO:probinson[2009-02-17]
OMIM:248510	Mannosidosis, beta		HP:0000007	PMID:9384606	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-07-01]
OMIM:248510	Mannosidosis, beta		HP:0000752	PMID:18565776	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-01]
OMIM:248510	Mannosidosis, beta		HP:0001249	PMID:18565776	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-01]
OMIM:248510	Mannosidosis, beta		HP:4000205	PMID:18565776	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:248510	Mannosidosis, beta		HP:0007108	OMIM:248510	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0001265	PMID:23084291	PCS		1/1			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0003202	PMID:23084291	PCS		1/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0008936	PMID:23084291	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0001298	PMID:23084291	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0002421	PMID:23084291	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0001344	PMID:23084291	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0000496	OMIM:614932	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0001266	PMID:23084291	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0001332	PMID:23084291	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0006829	PMID:23084291	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0002151	PMID:23084291	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0003593	PMID:23084291	PCS		2/2			C	HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0002490	PMID:23084291	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0100660	PMID:23084291	PCS		1/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0000518	OMIM:614932	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0000639	OMIM:614932	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0000407	OMIM:614932	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0000007	PMID:23084291	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0008872	PMID:23084291	PCS		1/2			P	HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0000762	PMID:23084291	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-10]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0001510	OMIM:614932	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0002415	OMIM:614932	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614932	Combined oxidative phosphorylation deficiency 13		HP:0006558	PMID:23084291	PCS		1/2			P	HPO:probinson[2021-07-10]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0003038	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0003016	OMIM:613091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0002980	OMIM:613091	TAS					P	HPO:skoehler[2013-10-22]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0002023	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0005257	OMIM:613091	TAS					P	HPO:probinson[2013-06-02]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0001156	OMIM:613091	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0004322	OMIM:613091	TAS					P	HPO:probinson[2015-02-22]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000062	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0001274	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0005054	OMIM:613091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0010984	OMIM:613091	TAS					I	HPO:probinson[2015-02-22]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0010297	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000895	OMIM:613091;PMID:23456818	PCS		12/20			P	HPO:lccarmody[2018-09-26];HPO:lccarmody[2018-09-26];HPO:skoehler[2015-02-22]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000773	OMIM:613091	TAS					P	HPO:probinson[2013-06-02]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000113	OMIM:613091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0003026	OMIM:613091	TAS					P	HPO:probinson[2013-06-02]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000110	OMIM:613091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000054	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000175	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0002650	OMIM:613091	TAS					P	HPO:skoehler[2013-06-03]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0001762	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0003022	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0011927	OMIM:613091	TAS					P	HPO:probinson[2013-06-02]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0002350	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0010454	OMIM:613091	TAS					P	HPO:skoehler[2013-06-03]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0011802	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0010579	OMIM:613091	TAS					P	HPO:skoehler[2013-06-03]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0100259	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0100258	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000888	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000007	OMIM:613091	TAS					I	HPO:probinson[2013-06-02]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0009556	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0002566	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000105	OMIM:613091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613091	Asphyxiating thoracic dystrophy 3		HP:0000204	OMIM:613091	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:217000	Complement component 2 deficiency		HP:0000979	OMIM:217000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217000	Complement component 2 deficiency		HP:0000007	OMIM:217000	IEA					I	HPO:iea[2009-02-17]
OMIM:217000	Complement component 2 deficiency		HP:0002725	OMIM:217000	IEA					P	HPO:iea[2009-02-17]
OMIM:614926	Perrault syndrome 2		HP:0000407	PMID:21464306	PCS		5/5			P	HPO:skoehler[2012-12-02];HPO:probinson[2020-08-10]
OMIM:614926	Perrault syndrome 2		HP:0000141	PMID:21464306	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-08-10]
OMIM:614926	Perrault syndrome 2		HP:0000007	PMID:21464306	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2020-08-10]
OMIM:614926	Perrault syndrome 2		HP:0010464	PMID:21464306	PCS		3/3	FEMALE		P	HPO:probinson[2020-08-10]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0003498	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0005575	PMID:36599939	PCS	HP:0003623	1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0005575	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0003593	PMID:37216524	PCS		2/2			C	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0005272	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0012596	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0002719	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001903	PMID:36599939	PCS	HP:0003623	1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001903	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0004719	PMID:36599939	PCS		1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001888	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0002714	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0000278	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0000358	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0004798	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0020181	PMID:36599939	PCS		1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0003026	PMID:36599939	PCS	HP:0030674	1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0003026	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0000431	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001882	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001981	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0002197	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001263	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0000093	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001419	PMID:36599939	PCS					I	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001878	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0000348	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0000527	PMID:36599939	PCS	HP:0003577	1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0000322	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001873	PMID:36599939	PCS	HP:0003623	1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001873	PMID:37216524	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0003259	PMID:36599939	PCS		1/1			P	HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001875	PMID:36599939	PCS	HP:0003623	1/1			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:301110	Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature		HP:0001875	PMID:37216524	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0004313	PMID:8890099	PCS		7/7			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0004432	PMID:8890099	PCS		1/7			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0005224	PMID:8890099	PCS		1/7			P	HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0002110	PMID:12370281	PCS		3/19			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0003593	PMID:12370281	PCS		12/19			C	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0010976	PMID:8890099	PCS		7/7			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0011108	PMID:12370281	PCS		3/19			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0001508	PMID:12370281	PCS		4/19			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0011463	PMID:12370281	PCS		7/19			C	HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0000509	PMID:12370281	PCS		3/19			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0002718	PMID:12370281	PCS					P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0000403	PMID:8890099	PCS		2/7			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0000007	PMID:8890099	PCS					I	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0006532	PMID:12370281	PCS		10/19			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0002205	PMID:12370281	PCS					P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0001875	PMID:12370281	PCS		6/19			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0002743	PMID:8890099;PMID:12370281	PCS		9/26			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-03-03];HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0003139	PMID:8890099	PCS		7/7			P	HPO:probinson[2022-03-03]
OMIM:601495	Agammaglobulinemia 1, autosomal recessive		HP:0002028	PMID:12370281	PCS		4/19			P	HPO:probinson[2022-03-03]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001371	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0002240	OMIM:617591	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0010702	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001508	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0002719	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001903	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001888	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0002716	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0009125	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0000956	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0012490	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0002910	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001744	OMIM:617591	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001369	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0003565	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0002155	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0025131	OMIM:617591	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0002829	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0100539	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0000509	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0100614	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001954	PMID:26524591	PCS					P	HP:probinson[2019-02-17]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0000007	OMIM:617591	IEA					I	HPO:skoehler[2019-04-18]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0000988	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0000246	OMIM:617591	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617591	Proteasome-Associated autoinflammatory syndrome 3		HP:0001873	OMIM:617591	IEA					P	HPO:skoehler[2019-02-15]
OMIM:213500	Cerebral angiopathy, dysphoric		HP:0000707	OMIM:213500	IEA					P	HPO:iea[2009-02-17]
OMIM:213500	Cerebral angiopathy, dysphoric		HP:0000007	OMIM:213500	IEA					I	HPO:iea[2009-02-17]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0000571	PMID:23236289	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0000750	PMID:23236289	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0001310	PMID:23236289	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0001272	PMID:23236289	PCS		2/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0002066	OMIM:615386	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0001263	PMID:23236289	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0002075	PMID:23236289	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0003593	PMID:23236289	PCS		3/3			C	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0001270	PMID:23236289	PCS		3/3			P	HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0002080	OMIM:615386	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0000639	PMID:23236289	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0008003	PMID:23236289	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0000007	PMID:23236289	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0002317	PMID:23236289	PCS		3/3			P	HPO:probinson[2023-02-19]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0001257	OMIM:615386	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0003677	OMIM:615386	TAS					C	HPO:skoehler[2013-10-06]
OMIM:615386	Spinocerebellar ataxia, autosomal recessive 14		HP:0001347	OMIM:615386	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:229850	Fryns syndrome		HP:0009937	OMIM:229850	TAS					P	HPO:probinson[2013-08-11]
OMIM:229850	Fryns syndrome		HP:0007759	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0010804	OMIM:229850	TAS					P	HPO:skoehler[2014-11-26]
OMIM:229850	Fryns syndrome		HP:0001212	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0002023	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0005257	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001250	OMIM:229850	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229850	Fryns syndrome		HP:0000280	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000316	OMIM:229850	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229850	Fryns syndrome		HP:0000954	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0003826	OMIM:229850	IEA					C	HPO:skoehler[2010-06-20]
OMIM:229850	Fryns syndrome		HP:0006278	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0009623	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0002139	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001249	OMIM:229850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000175	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0002032	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0010310	OMIM:229850	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229850	Fryns syndrome		HP:0012385	OMIM:229850	TAS					P	HPO:skoehler[2013-10-22]
OMIM:229850	Fryns syndrome		HP:0000007	OMIM:229850	IEA					I	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000568	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0007036	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001539	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000048	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000047	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000883	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0009778	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000204	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000369	OMIM:229850	TAS					P	HPO:skoehler[2010-06-18]
OMIM:229850	Fryns syndrome		HP:0000126	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000885	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000049	OMIM:229850	TAS					P	HPO:skoehler[2013-07-17]
OMIM:229850	Fryns syndrome		HP:0002245	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001792	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000343	OMIM:229850	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229850	Fryns syndrome		HP:0002089	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000463	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000581	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001274	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0011039	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001629	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0009882	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001305	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000813	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001748	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000154	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001561	OMIM:229850	IEA		14%			P	HPO:skoehler[2010-06-20]
OMIM:229850	Fryns syndrome		HP:0000431	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000475	OMIM:229850	TAS		20/20			P	HPO:skoehler[2010-06-20];HPO:skoehler[2013-08-11]
OMIM:229850	Fryns syndrome		HP:0001520	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000073	OMIM:229850	TAS					P	HPO:probinson[2013-08-11]
OMIM:229850	Fryns syndrome		HP:0002251	OMIM:229850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000470	OMIM:229850	TAS					P	HPO:skoehler[2013-08-11]
OMIM:229850	Fryns syndrome		HP:0045025	OMIM:229850	IEA					P	HPO:skoehler[2018-10-08]
OMIM:229850	Fryns syndrome		HP:0007096	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001838	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000308	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0009473	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0009112	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000107	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001631	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000028	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0002247	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0002566	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0000104	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:229850	Fryns syndrome		HP:0001798	OMIM:229850	IEA					P	HPO:iea[2009-02-17]
OMIM:241520	Hypophosphatemic rickets, autosomal recessive		HP:0001363	OMIM:241520	IEA					P	HPO:iea[2009-02-17]
OMIM:241520	Hypophosphatemic rickets, autosomal recessive		HP:0000407	OMIM:241520	IEA					P	HPO:iea[2009-02-17]
OMIM:241520	Hypophosphatemic rickets, autosomal recessive		HP:0011001	OMIM:241520	IEA					P	HPO:iea[2009-02-17]
OMIM:241520	Hypophosphatemic rickets, autosomal recessive		HP:0002748	OMIM:241520	IEA					P	HPO:skoehler[2010-06-20]
OMIM:241520	Hypophosphatemic rickets, autosomal recessive		HP:0000007	OMIM:241520	IEA					I	HPO:iea[2009-02-17]
OMIM:241520	Hypophosphatemic rickets, autosomal recessive		HP:0004912	OMIM:241520	TAS					P	HPO:probinson[2009-02-17]
OMIM:241520	Hypophosphatemic rickets, autosomal recessive		HP:0002148	OMIM:241520	IEA					P	HPO:skoehler[2010-06-18]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001276	PMID:25620207	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0003577	PMID:25620207	PCS		3/3			C	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0010804	OMIM:614098	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001371	PMID:25620207	PCS		1/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001250	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0002781	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0003292	PMID:25620207	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001090	OMIM:614098	TAS					P	HPO:skoehler[2013-10-13]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0009064	PMID:25620207	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001508	OMIM:614098	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0007485	PMID:25620207	PCS		1/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000218	PMID:25620207	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0006532	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000212	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0005328	OMIM:614098	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001347	OMIM:614098	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0002179	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0006956	PMID:25620207	PCS		2/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000252	OMIM:614098	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001561	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0002650	PMID:25620207	PCS		4/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-05];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000430	PMID:25620207	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0002373	PMID:25620207	PCS		1/3			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000194	PMID:25620207	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001263	PMID:25620207	PCS		2/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0005320	PMID:25620207	PCS		2/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0001285	PMID:25620207	PCS		1/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0002093	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0009933	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000520	PMID:25620207	PCS		2/3			P	HPO:skoehler[2013-10-13];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000586	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000322	OMIM:614098	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000006	PMID:25620207	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000347	PMID:25620207	PCS		1/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-05]
OMIM:614098	Keppen-Lubinsky syndrome		HP:0000446	PMID:25620207	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0002344	PMID:17646634	PCS		4/4			P	HPO:probinson[2023-06-27];HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0007082	PMID:17646634	PCS		1/4			P	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0006956	PMID:17646634	PCS		1/4			P	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0001355	PMID:17646634	PCS		3/4			P	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0011463	PMID:17646634	PCS		3/4			C	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0003593	PMID:17646634	PCS		1/4			C	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:6000447	PMID:18519871	PCS		7/7			P	HPO:probinson[2024-04-03]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0000007	PMID:11704758	PCS					I	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0002505	PMID:17646634	PCS		1/4			P	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0002500	PMID:17646634	PCS		1/4			P	HPO:probinson[2023-06-27]
OMIM:620315	Leukoencephalopathy with vanishing white matter 5, with or without ovarian failure		HP:0001259	PMID:17646634	PCS		3/4			P	HPO:probinson[2023-06-27]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0000155	PMID:31827281	PCS		8/14			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0011110	PMID:31827281	PCS		3/7			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0003493	PMID:31827281	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0002240	PMID:31827280;PMID:31827281	PCS		3/12			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0001954	PMID:31827280;PMID:31827281	PCS		11/12			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0002716	PMID:31827280;PMID:31827281	PCS		11/12			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0001935	PMID:31827280	PCS		5/5			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0002923	PMID:31827281	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0000006	PMID:31827281	PCS					I	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0001744	PMID:31827280;PMID:31827281	PCS		7/12			P	HPO:probinson[2020-07-01]
OMIM:618852	Autoinflammation with episodic fever and lymphadenopathy		HP:0002027	PMID:31827280;PMID:31827281	PCS		5/12			P	HPO:probinson[2020-07-01]
OMIM:619594	Epidermolysis bullosa simplex 2C, localized		HP:0025088	PMID:28425111	PCS		1/1			P	HPO:probinson[2021-11-15]
OMIM:619594	Epidermolysis bullosa simplex 2C, localized		HP:0003577	PMID:28425111	PCS		1/1			C	HPO:probinson[2022-03-27]
OMIM:619594	Epidermolysis bullosa simplex 2C, localized		HP:0007446	PMID:28425111;PMID:7688477	PCS		21/21			P	HPO:probinson[2021-11-15]
OMIM:619594	Epidermolysis bullosa simplex 2C, localized		HP:0000006	PMID:7688477	TAS					I	HPO:probinson[2021-11-15]
OMIM:619594	Epidermolysis bullosa simplex 2C, localized		HP:0001810	PMID:28425111	PCS		1/1			P	HPO:probinson[2021-11-15]
OMIM:261800	Pierre Robin syndrome		HP:0000175	OMIM:261800	IEA					P	HPO:iea[2009-02-17]
OMIM:261800	Pierre Robin syndrome		HP:0002781	OMIM:261800	IEA					P	HPO:iea[2009-02-17]
OMIM:261800	Pierre Robin syndrome		HP:0000162	OMIM:261800	IEA					P	HPO:iea[2009-02-17]
OMIM:261800	Pierre Robin syndrome		HP:0000007	OMIM:261800	IEA					I	HPO:iea[2009-02-17]
OMIM:261800	Pierre Robin syndrome		HP:0008872	OMIM:261800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:261800	Pierre Robin syndrome		HP:0001648	OMIM:261800	IEA					P	HPO:iea[2009-02-17]
OMIM:261800	Pierre Robin syndrome		HP:0000201	OMIM:261800	TAS					P	HPO:skoehler[2009-02-17]
OMIM:261800	Pierre Robin syndrome		HP:0000347	OMIM:261800	IEA					P	HPO:iea[2009-02-17]
OMIM:261800	Pierre Robin syndrome		HP:0002643	OMIM:261800	IEA					P	HPO:iea[2009-02-17]
OMIM:611876	Brugada syndrome 4		HP:0012232	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:611876	Brugada syndrome 4		HP:0005110	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:611876	Brugada syndrome 4		HP:0001279	PMID:17224476	PCS					P	HPO:probinson[2013-04-03]
OMIM:611876	Brugada syndrome 4		HP:0000006	PMID:17224476	PCS					I	HPO:probinson[2013-01-09]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002188	PMID:27102849	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0003311	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0004322	PMID:27102849	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0001371	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0001250	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0001251	PMID:27102849	PCS		7/7			P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000280	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0003071	OMIM:300232	TAS		20/20			P	HPO:probinson[2013-04-08];HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0012704	OMIM:300232	TAS					P	HPO:skoehler[2014-04-04]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0009381	OMIM:300232	TAS					P	HPO:probinson[2012-06-10]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000639	PMID:27102849	PCS		7/7			P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0011463	PMID:27102849	PCS		7/7			C	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000316	PMID:27102849	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002812	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0001769	OMIM:300232	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0001169	OMIM:300232	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0003202	PMID:27102849	PCS		7/7		HP:0003676	P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002751	PMID:27102849	PCS		4/4			P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000574	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002750	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002079	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0003487	PMID:27102849	PCS		2/4			P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000294	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002273	PMID:27102849	PCS		4/4			P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0011800	PMID:27102849	PCS		4/4			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0001419	PMID:27102849	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000926	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002869	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0006423	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000884	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002942	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0006028	OMIM:300232	TAS					P	HPO:probinson[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000883	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000369	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0003016	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0001156	PMID:27102849	PCS		4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000463	PMID:27102849	PCS		4/4			P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0010585	OMIM:300232	TAS					P	HPO:probinson[2013-04-08]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0100864	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000218	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000455	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002651	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002376	PMID:27102849	PCS	HP:0011463	7/7			P	HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000272	PMID:27102849	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000470	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0005280	PMID:27102849	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000907	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0008789	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0000543	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:300232	Spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration		HP:0002645	OMIM:300232	IEA					P	HPO:iea[2009-02-17]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0000100	OMIM:613913	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0000793	OMIM:613913	TAS		26%			P	HPO:skoehler[2012-11-18]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0005421	OMIM:613913	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0002719	OMIM:613913	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0009056	OMIM:613913	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0000292	OMIM:613913	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0000790	OMIM:613913	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0009125	OMIM:613913	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0000093	OMIM:613913	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0003745	OMIM:613913	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613913	Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis		HP:0009019	OMIM:613913	TAS					P	HPO:skoehler[2012-10-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000286	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0002047	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0002089	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001371	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001373	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0009381	OMIM:312150	TAS				HP:0012828	P	HPO:probinson[2012-06-10]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000316	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0005905	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001989	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0002659	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000476	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001961	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000457	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000175	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001561	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001040	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000969	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0002948	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001999	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001417	OMIM:312150	TAS					I	HPO:skoehler[2013-05-29]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0001511	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000883	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000204	OMIM:312150	TAS					P	HPO:probinson[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000347	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0000369	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:312150	Multiple pterygium syndrome, X-linked		HP:0003634	OMIM:312150	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0000121	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002663	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002982	OMIM:300554	TAS					P	HPO:probinson[2012-05-01]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0003013	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002980	OMIM:300554	TAS					P	HPO:probinson[2012-05-01]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0004322	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0000083	OMIM:300554	TAS	HP:0003581				P	HPO:probinson[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0010502	OMIM:300554	TAS					P	HPO:probinson[2012-05-01]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0012622	OMIM:300554	TAS					P	HPO:probinson[2014-01-18]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002979	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0000117	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002757	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0000114	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0004912	OMIM:300554	TAS					P	HPO:probinson[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002753	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0003029	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002653	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002752	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0003126	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0003025	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0003020	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002150	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0031415	OMIM:300554	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0001419	OMIM:300554	IEA					I	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002748	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002749	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0000787	OMIM:300554	IEA					P	HPO:iea[2009-02-17]
OMIM:300554	Hypophosphatemic rickets, X-linked recessive		HP:0002148	OMIM:300554	IEA					P	HPO:skoehler[2010-06-18]
OMIM:618846	Diets-Jongmans syndrome		HP:0030853	PMID:30929739	PCS	HP:0003577	1/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000365	PMID:30929739	PCS		4/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000023	PMID:30929739	PCS	HP:0003577	2/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0004322	PMID:30929739	PCS		8/16			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001250	PMID:30929739	PCS		3/15			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001290	PMID:30929739	PCS	HP:0011463	5/13			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001270	PMID:30929739	PCS		14/16			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001629	PMID:30929739	PCS		1/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000718	PMID:30929739	PCS		1/15			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0008872	PMID:30929739	PCS	HP:0003623	9/15			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000219	PMID:30929739	PCS		12/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0009765	PMID:30929739	PCS		6/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000455	PMID:30929739	PCS		14/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001623	PMID:30929739	PCS		4/14			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001249	PMID:30929739	PCS					P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000776	PMID:30929739	PCS	HP:0003577	2/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000154	PMID:30929739	PCS		12/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001561	PMID:30929739	PCS		1/14			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001385	PMID:30929739	PCS	HP:0003577	1/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000750	PMID:30929739	PCS		16/16			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0031936	PMID:30929739	PCS		5/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001382	PMID:30929739	PCS		5/16			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0002171	PMID:30929739	PCS		1/12			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0400004	PMID:30929739	PCS		9/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0007074	PMID:30929739	PCS		1/12			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000729	PMID:30929739	PCS		3/15			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0011671	PMID:30929739	PCS	HP:0003577	1/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0001537	PMID:30929739	PCS	HP:0003577	2/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000307	PMID:30929739	PCS		12/17			P	HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0007018	PMID:30929739	PCS		4/15			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000047	PMID:30929739	PCS	HP:0003577	1/8	MALE		P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000006	PMID:30929739	PCS					I	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0002247	PMID:30929739	PCS	HP:0003577	1/16			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618846	Diets-Jongmans syndrome		HP:0000028	PMID:30929739	PCS		1/8	MALE		P	HPO:probinson[2020-06-28]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002069	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001298	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0010529	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002188	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000365	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002540	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000486	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002384	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002066	PMID:34375587;PMID:28180184	PCS		4/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0010808	PMID:28180184	PCS		1/1			P	HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001252	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001251	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001290	PMID:34375587;PMID:28180184	PCS		2/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0032794	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0033725	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000718	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000712	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0003429	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0025336	PMID:34375587;PMID:28180184	PCS		2/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001249	PMID:34375587;PMID:28180184	PCS		8/8			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0003623	PMID:28180184	PCS		1/1			C	HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001188	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0006934	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000252	PMID:28180184	PCS		1/1			P	HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001344	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001266	PMID:28180184	PCS		1/1			P	HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001263	PMID:34375587;PMID:28180184	PCS		12/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0100023	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0011097	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000729	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002509	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002307	PMID:28180184	PCS		1/1			P	HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000961	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002104	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000006	PMID:28180184	PCS					I	HPO:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0007859	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001272	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0001270	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0040082	PMID:34375587;PMID:28180184	PCS		3/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0100703	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0100704	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000739	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0020221	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000733	PMID:28180184	PCS		1/1			P	HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000736	PMID:34375587;PMID:28180184	PCS		2/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002119	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0008936	PMID:34375587	PCS		3/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0002179	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000750	PMID:34375587;PMID:28180184	PCS		9/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0031936	PMID:34375587;PMID:28180184	PCS		5/12			P	HP:probinson[2021-11-10];HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0012510	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0100710	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0000749	PMID:28180184	PCS		1/1			P	HPO:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0032792	PMID:34375587	PCS		2/11			P	HP:probinson[2021-11-10]
OMIM:619580	Neurodevelopmental disorder with impaired language and ataxia and with or without seizures		HP:0007018	PMID:34375587	PCS		1/11			P	HP:probinson[2021-11-10]
OMIM:611863	Microtia - eye coloboma - imperforation of the nasolacrimal duct		HP:0008551	OMIM:611863	IEA					P	HPO:skoehler[2015-01-27]
OMIM:611863	Microtia - eye coloboma - imperforation of the nasolacrimal duct		HP:0000006	OMIM:611863	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003236	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0010628	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003731	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003391	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003707	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0011462	PMID:11822024	PCS		2/2			C	HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003749	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0002515	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0007126	PMID:11822024	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003547	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003701	PMID:11822024	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003724	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003722	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0001265	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003687	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003401	PMID:11822024	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0001284	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003560	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003738	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0000007	PMID:11822024	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0002505	PMID:11822024	PCS	HP:0003584	1/2			P	HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003677	PMID:11822024	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003458	PMID:11822024	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0003557	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:254110	Muscular dystrophy, limb-girdle, type 2H		HP:0008988	OMIM:254110	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0001342	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0003345	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0002664	OMIM:171300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0003574	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0001095	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0000093	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0003072	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0000957	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0000519	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0000975	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0001635	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0001649	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0000006	OMIM:171300	IEA					I	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0000875	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0001920	OMIM:171300	IEA					P	HPO:iea[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0001028	OMIM:171300	TAS					P	HPO:probinson[2009-02-17]
OMIM:171300	PHEOCHROMOCYTOMA		HP:0002666	OMIM:171300	TAS					P	HPO:probinson[2009-02-17]
OMIM:618847	Immunodeficiency 66		HP:0001287	PMID:26224645	PCS		1/1			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618847	Immunodeficiency 66		HP:0200039	PMID:26224645	PCS		1/1			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618847	Immunodeficiency 66		HP:0001581	PMID:26224645	PCS		1/1			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618847	Immunodeficiency 66		HP:0100806	PMID:26224645	PCS		1/1			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618847	Immunodeficiency 66		HP:0000007	PMID:26224645	TAS					I	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618847	Immunodeficiency 66		HP:0031379	PMID:26224645	PCS		1/1			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618847	Immunodeficiency 66		HP:0410017	PMID:26224645	PCS		1/1			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0002069	PMID:19699128	PCS		1/5			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0003236	PMID:19699128	PCS		1/3			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0003652	PMID:12754706	PCS		15/15			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001250	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0003593	PMID:19699128;PMID:12754706	PCS		2/20			C	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0031964	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0011463	PMID:19699128;PMID:12754706	PCS		10/20			C	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0002913	PMID:19699128	PCS		1/5			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001943	PMID:19699128;PMID:12754706;PMID:19880769	PCS		10/21			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001987	PMID:19699128	PCS		2/5			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0002615	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001522	PMID:19699128	PCS		1/5			C	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001942	PMID:19699128;PMID:19880769	PCS		3/6			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001644	PMID:19699128;PMID:12754706	PCS		7/20			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0003623	PMID:19699128;PMID:12754706;PMID:19880769	PCS		8/21			C	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0003326	PMID:19699128	PCS		1/3			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001342	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0031956	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0003621	PMID:19699128	PCS		1/5			C	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0002151	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001263	PMID:19699128	PCS		2/3			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:4000141	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0005180	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0031185	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0009830	PMID:12754706	PCS		7/13			P	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0000007	PMID:8651282	PCS					I	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0003811	PMID:19699128	PCS		1/5			C	HPO:probinson[2023-07-03]
OMIM:620300	Mitochondrial trifunctional protein deficiency 2		HP:0001653	PMID:19880769	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:300555	Dent disease 2		HP:0000121	PMID:15627218	PCS		1/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0003236	PMID:15627218	PCS		2/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0003126	PMID:15627218	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0031956	PMID:15627218	PCS		2/5			P	HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0003355	PMID:15627218	PCS		2/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0004322	PMID:15627218	PCS		1/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0002150	PMID:15627218	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0012622	OMIM:300555	TAS					P	HPO:skoehler[2014-01-18]
OMIM:300555	Dent disease 2		HP:0031964	PMID:15627218	PCS		2/5			P	HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0100543	OMIM:300555	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300555	Dent disease 2		HP:0011463	OMIM:300555	TAS					C	HPO:skoehler[2012-10-14]
OMIM:300555	Dent disease 2		HP:0001419	PMID:15627218	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0011342	PMID:15627218	PCS		3/4			P	HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0001537	OMIM:300555	TAS		HP:0040283			P	HPO:skoehler[2012-11-28]
OMIM:300555	Dent disease 2		HP:0025435	PMID:15627218	PCS		2/5			P	HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0000114	PMID:15627218	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2021-07-10]
OMIM:300555	Dent disease 2		HP:0002148	PMID:15627218	PCS		3/5			P	HPO:probinson[2021-07-10]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0000252	OMIM:236795	IEA					P	HPO:iea[2009-02-17]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0005974	OMIM:236795	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0001993	OMIM:236795	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0003355	OMIM:236795	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0001508	OMIM:236795	IEA					P	HPO:iea[2009-02-17]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0006906	OMIM:236795	IEA					P	HPO:iea[2009-02-17]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0001999	OMIM:236795	IEA					P	HPO:iea[2009-02-17]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0000007	OMIM:236795	IEA					I	HPO:iea[2009-02-17]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0002269	OMIM:236795	IEA					P	HPO:iea[2009-02-17]
OMIM:236795	3-hydroxyisobutyric aciduria		HP:0003128	OMIM:236795	IEA					P	HPO:iea[2009-02-17]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0002223	PMID:28285769	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000561	PMID:28285769	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0004322	PMID:28285769	PCS		6/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000085	PMID:28285769	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0010049	PMID:28285769	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0010761	PMID:28285769	PCS					P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0100255	OMIM:250410	TAS					P	HPO:skoehler[2010-06-18]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0045075	PMID:28285769	IEA		2/10			P	HPO:probinson[2019-09-02];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000957	PMID:28285769	PCS		2/10			P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0011463	PMID:28285769	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0012471	PMID:28285769	PCS					P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000510	PMID:28285769	PCS		6/10			P	HPO:iea[2009-02-17];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001763	PMID:28285769	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001249	PMID:28285769	PCS		4/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000494	PMID:28285769	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0011968	PMID:28285769	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001263	PMID:28285769	PCS		4/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0033379	PMID:28285769	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0009890	PMID:28285769	PCS					P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0002308	PMID:28285769	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000007	PMID:28285769	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0007994	PMID:28285769	IEA					P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000400	PMID:28285769	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000369	PMID:28285769	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0003577	PMID:28285769	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001792	PMID:28285769	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000662	PMID:28285769	PCS	HP:0003621	3/3			P	HPO:probinson[2019-09-02];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001596	PMID:28285769	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001156	PMID:28285769	PCS		9/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0030674	PMID:28285769	PCS		2/8			C	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0002120	PMID:28285769	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0005871	OMIM:250410	TAS					P	HPO:skoehler[2009-02-17];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0008070	PMID:28285769	PCS		2/10			P	HPO:probinson[2019-09-02];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001629	PMID:28285769	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0009882	PMID:28285769	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001822	PMID:28285769	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000653	PMID:28285769	IEA		2/10			P	HPO:probinson[2019-09-02];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000256	PMID:10420199	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001363	PMID:28285769	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0003621	PMID:28285769	PCS		4/8			C	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000750	PMID:28285769	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0031936	PMID:28285769	PCS		3/10			P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:6000460	PMID:28285769	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000430	PMID:28285769	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0025159	PMID:28285769	PCS					P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0008064	PMID:28285769	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000107	PMID:28285769	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000546	PMID:28285769	PCS		9/10			P	HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0002007	PMID:28285769	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0001511	PMID:28285769	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-05-26]
OMIM:250410	Retinitis pigmentosa with or without skeletal anomalies		HP:0000347	PMID:28285769	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-02]
OMIM:613912	Complement factor D deficiency		HP:0002718	PMID:11457876	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613912	Complement factor D deficiency		HP:0000007	PMID:11457876	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613912	Complement factor D deficiency		HP:0008338	PMID:11457876	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0004303	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003236	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-18]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003750	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003198	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003394	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003560	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0012378	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0009071	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003737	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0000006	OMIM:123320	IEA					I	HPO:iea[2009-02-17]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003710	OMIM:123320	IEA					P	HPO:iea[2009-02-17]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003458	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:123320	Creatine phosphokinase, elevated serum		HP:0003326	PMID:9660505	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000286	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000486	PMID:33909990	PCS		3/30			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000343	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0004322	PMID:33909990	PCS		0/30			P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000540	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0001250	PMID:33909990	PCS		3/32			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0001252	PMID:33909990	PCS		18/30			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0003593	PMID:33909990	PCS					C	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0002020	PMID:33909990	PCS	HP:0003593				P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0011220	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000219	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000411	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000256	PMID:33909990	PCS		2/29			P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000278	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0001249	PMID:33909990	PCS		22/29			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000154	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000252	PMID:33909990	PCS		1/29			P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000750	PMID:33909990	PCS		28/30			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000431	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0002750	PMID:33909990	PCS		0/30			P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000276	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000232	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0001382	PMID:33909990	PCS		17/32			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0045025	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000709	PMID:33909990	PCS		4/30			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000708	PMID:33909990	PCS		18/30			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000729	PMID:33909990	PCS		12/29			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000629	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000007	PMID:33909990	PCS					I	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000545	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000028	PMID:33909990	PCS		1/17			P	HPO:probinson[2022-02-04]
OMIM:619595	Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities		HP:0000303	PMID:33909990	PCS					P	HPO:probinson[2022-02-04]
OMIM:618853	Anauxetic dysplasia 3		HP:0003510	PMID:31250547	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0001792	PMID:31250547	PCS		1/1			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0002980	PMID:31250547	PCS		3/4			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0001156	PMID:31250547	PCS		4/4			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000260	PMID:31250547	PCS		2/4			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0003177	PMID:31250547	PCS		3/4			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0002020	PMID:31250547	PCS		3/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0001290	PMID:31250547	PCS		4/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0010049	PMID:31250547	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0001270	PMID:31250547	PCS		4/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0004060	PMID:31250547	PCS		3/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0030043	PMID:31250547	PCS		1/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0002857	PMID:31250547	PCS		1/1			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000774	PMID:31250547	PCS		2/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000278	PMID:31250547	PCS		1/1			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0009844	PMID:31250547	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000677	PMID:31250547	PCS		1/2			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000973	PMID:31250547	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0003423	PMID:31250547	PCS		2/2			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0011968	PMID:31250547	PCS		2/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0001382	PMID:31250547	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0002176	PMID:31250547	PCS		1/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0001263	PMID:31250547	PCS		4/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0003021	PMID:31250547	PCS		4/4			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0011800	PMID:31250547	PCS		2/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0011229	PMID:31250547	PCS		3/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0005280	PMID:31250547	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0009890	PMID:31250547	PCS		3/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000926	PMID:31250547	PCS		4/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0005819	PMID:31250547	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0002209	PMID:31250547	PCS		3/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000767	PMID:31250547	PCS		3/3			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0000007	PMID:31250547	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0002205	PMID:31250547	PCS		2/5			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0001357	PMID:31250547	PCS		2/2			P	HPO:probinson[2020-06-27]
OMIM:618853	Anauxetic dysplasia 3		HP:0004568	PMID:31250547	PCS		2/5			P	HPO:probinson[2020-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0003621	PMID:12707859	PCS		1/2			C	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0031936	PMID:12707859	PCS		1/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0002120	PMID:12707859	PCS		2/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0002352	PMID:11835386;PMID:12707859	PCS		4/4			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0001260	PMID:12707859	PCS		1/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0007371	PMID:12707859	PCS		2/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0011463	PMID:12707859	PCS		1/2			C	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0000869	PMID:12707859	PCS		1/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0000007	PMID:11835386	PCS					I	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0002317	PMID:12707859	PCS		1/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0000648	PMID:12707859	PCS		2/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0002119	PMID:12707859	PCS		2/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0001257	PMID:12707859	PCS		2/2			P	HPO:probinson[2023-06-27]
OMIM:620314	Leukoencephalopathy with vanishing white matter 4, with or without ovarian failure		HP:0000786	PMID:12707859	PCS		1/2			P	HPO:probinson[2023-06-27]
OMIM:167210	Pachyonychia congenita 2		HP:0000695	PMID:7539673	PCS	HP:0003577	1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:167210	Pachyonychia congenita 2		HP:0002164	OMIM:167210	IEA					P	HPO:iea[2009-02-17]
OMIM:167210	Pachyonychia congenita 2		HP:0045075	OMIM:167210	TAS					P	HPO:probinson[2022-05-07]
OMIM:167210	Pachyonychia congenita 2		HP:0025084	OMIM:167210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:167210	Pachyonychia congenita 2		HP:0030318	PMID:7539673	PCS					P	HPO:probinson[2022-09-02]
OMIM:167210	Pachyonychia congenita 2		HP:0011359	OMIM:167210	IEA					P	HPO:iea[2012-03-01]
OMIM:167210	Pachyonychia congenita 2		HP:0008392	OMIM:167210	IEA					P	HPO:iea[2012-03-01]
OMIM:167210	Pachyonychia congenita 2		HP:0200040	PMID:7539673	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-09-02]
OMIM:167210	Pachyonychia congenita 2		HP:0012035	PMID:9618173	PCS					P	HPO:probinson[2012-07-27]
OMIM:167210	Pachyonychia congenita 2		HP:0001609	PMID:7539673	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:167210	Pachyonychia congenita 2		HP:0002209	OMIM:167210	IEA					P	HPO:iea[2009-02-17]
OMIM:167210	Pachyonychia congenita 2		HP:0007410	OMIM:167210	IEA					P	HPO:iea[2009-02-17]
OMIM:167210	Pachyonychia congenita 2		HP:0000972	PMID:7539673	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:167210	Pachyonychia congenita 2		HP:0008404	PMID:7539673	PCS		4/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-02]
OMIM:167210	Pachyonychia congenita 2		HP:0002745	PMID:7539673	PCS		0/4			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-09-02]
OMIM:167210	Pachyonychia congenita 2		HP:0000006	PMID:7539673	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:178330	Ptosis, strabismus, and ectopic pupils		HP:0000486	OMIM:178330	IEA					P	HPO:iea[2009-02-17]
OMIM:178330	Ptosis, strabismus, and ectopic pupils		HP:0000508	OMIM:178330	IEA					P	HPO:iea[2009-02-17]
OMIM:178330	Ptosis, strabismus, and ectopic pupils		HP:0000006	OMIM:178330	IEA					I	HPO:iea[2009-02-17]
OMIM:231950	Glutathioninuria		HP:0002345	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0000486	OMIM:231950	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:231950	Glutathioninuria		HP:0002099	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0001274	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0001263	PMID:29483667	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0000020	PMID:29483667	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0002075	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0003593	PMID:29483667	PCS		2/2			C	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0034445	PMID:29483667	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0002282	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:6000578	PMID:29483667	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:231950	Glutathioninuria		HP:0034586	PMID:29483667	PCS		2/2			P	HPO:probinson[2023-03-31]
OMIM:231950	Glutathioninuria		HP:0000007	PMID:29483667	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0000964	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0000601	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0002019	PMID:29483667	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0001249	OMIM:231950	IEA		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-06]
OMIM:231950	Glutathioninuria		HP:0001337	OMIM:231950	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:231950	Glutathioninuria		HP:0001347	PMID:29483667	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002982	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0005897	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000365	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0004586	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0003179	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000260	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0005474	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:6000871	PMID:18798308	PCS		13/25			P	HPO:probinson[2024-08-03]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0008873	OMIM:259420	TAS					P	HPO:probinson[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002757	OMIM:259420	TAS					P	HPO:probinson[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002650	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0003023	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0003100	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000592	OMIM:259420	TAS	HP:0003577				P	HPO:probinson[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002691	OMIM:259420	TAS					P	HPO:probinson[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002092	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002808	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000703	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002007	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0008921	OMIM:259420	TAS					P	HPO:probinson[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0002645	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0005758	OMIM:259420	TAS					P	HPO:skoehler[2013-10-22]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000883	OMIM:259420	TAS					P	HPO:probinson[2020-07-19]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000006	OMIM:259420	IEA					I	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000347	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0000325	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:259420	Osteogenesis imperfecta, type III		HP:0005855	OMIM:259420	IEA					P	HPO:iea[2009-02-17]
OMIM:610599	Retinitis pigmentosa 36		HP:0000550	OMIM:610599	TAS					P	HPO:probinson[2013-02-28]
OMIM:610599	Retinitis pigmentosa 36		HP:0007737	PMID:20507925	PCS					P	HPO:probinson[2013-02-28];HPO:probinson[2020-07-24]
OMIM:610599	Retinitis pigmentosa 36		HP:0000608	OMIM:610599	TAS					P	HPO:probinson[2013-02-28]
OMIM:610599	Retinitis pigmentosa 36		HP:0000007	PMID:20507925	PCS					I	HPO:probinson[2013-02-28];HPO:probinson[2020-07-24]
OMIM:610599	Retinitis pigmentosa 36		HP:0000510	OMIM:610599	TAS					P	HPO:probinson[2013-02-28]
OMIM:610599	Retinitis pigmentosa 36		HP:0000543	OMIM:610599	TAS					P	HPO:probinson[2013-02-28]
OMIM:610599	Retinitis pigmentosa 36		HP:0007843	OMIM:610599	TAS					P	HPO:probinson[2013-02-28]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0003621	PMID:11106718	PCS		1/8			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0003596	PMID:20083571;PMID:11106718	PCS		4/12			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0003593	PMID:20083571;PMID:11106718	PCS		3/12			C	HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0005110	PMID:20083571	PCS		0/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0030682	PMID:20083571	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0033534	PMID:20083571	PCS		2/2			P	HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:6000313	PMID:11684629	PCS		2/20			P	HPO:probinson[2024-02-27]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0012664	PMID:20083571;PMID:11684629	PCS		16/23			P	HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0033755	PMID:20083571;PMID:11106718	PCS		7/7			P	HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0011462	PMID:20083571;PMID:11106718	PCS		3/12			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0011461	PMID:20083571	PCS		1/4			C	HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0001712	OMIM:601494	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0001635	PMID:20083571;PMID:11684629;PMID:11106718	PCS		19/32			P	HPO:probinson[2022-07-03];HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0001657	PMID:11684629	PCS		3/20			P	HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0000006	PMID:11106718	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0001645	PMID:11106718	PCS		5/13			P	HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0001644	PMID:11684629;PMID:11106718	PCS		24/30			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03];HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:601494	Cardiomyopathy, dilated, 1D		HP:0001688	PMID:11684629	PCS		2/20			P	HPO:probinson[2022-07-03]
OMIM:243450	Isovaleric acid, inability to smell		HP:0000007	OMIM:243450	IEA					I	HPO:iea[2009-02-17]
OMIM:243450	Isovaleric acid, inability to smell		HP:0000458	OMIM:243450	TAS					P	HPO:probinson[2009-02-17]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0010946	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0004322	PMID:36586412	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002046	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000062	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002580	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000086	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002020	PMID:36586412	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000085	PMID:24721225	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0003593	PMID:24721225	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0001270	PMID:36586412	PCS		18/26			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0012330	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0012531	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0001647	PMID:24721225	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0001627	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002579	PMID:36586412	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000378	PMID:24721225	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0001423	PMID:24721225	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002019	PMID:36586412	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0001249	PMID:36586412	PCS		17/20			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0003502	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002751	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000076	PMID:36586412	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000252	PMID:36586412	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000750	PMID:36586412	PCS		26/26			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002650	PMID:36586412	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0001382	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0003067	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0012378	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0010677	PMID:24721225	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000708	PMID:36586412	PCS		5/8			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0002808	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000729	PMID:36586412	PCS		15/21			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0012020	PMID:24721225	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000805	PMID:36586412	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000107	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0001737	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000488	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000047	PMID:36586412;PMID:24721225	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0007018	PMID:24721225	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000028	PMID:36586412	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:301111	Intellectual developmental disorder, X-linked 112		HP:0000545	PMID:36586412	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:614927	Ectodermal dysplasia 5, Hair/nail type		HP:0008391	PMID:15675952	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2024-06-25]
OMIM:614927	Ectodermal dysplasia 5, Hair/nail type		HP:0003577	PMID:15675952	PCS					C	HPO:probinson[2024-06-25]
OMIM:614927	Ectodermal dysplasia 5, Hair/nail type		HP:0002209	PMID:15675952	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2024-06-25]
OMIM:614927	Ectodermal dysplasia 5, Hair/nail type		HP:0000007	PMID:15675952	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2024-06-25]
OMIM:614927	Ectodermal dysplasia 5, Hair/nail type		HP:0001802	PMID:15675952	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2024-06-25]
OMIM:614927	Ectodermal dysplasia 5, Hair/nail type		HP:0000653	PMID:15675952	PCS					P	HPO:probinson[2024-06-25]
OMIM:614927	Ectodermal dysplasia 5, Hair/nail type		HP:0045075	PMID:15675952	PCS					P	HPO:probinson[2024-06-25]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0003577	OMIM:613090	IEA					C	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0003113	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0000083	OMIM:613090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001252	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001290	OMIM:613090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0010984	OMIM:613090	TAS					I	HPO:probinson[2024-08-03]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001270	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0012605	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001508	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0000859	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0002914	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001249	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001622	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001265	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001561	OMIM:613090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0001563	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0012213	OMIM:613090	TAS					P	HPO:skoehler[2013-03-15]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0003081	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0000969	OMIM:613090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0004909	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0000407	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0002902	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0002900	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0000103	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613090	Bartter syndrome, type 4B, neonatal, with sensorineural deafness		HP:0000127	OMIM:613090	IEA					P	HPO:skoehler[2010-06-19]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0030799	PMID:21378380	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0003774	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0008905	PMID:21378380	PCS		2/2			P	HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0001156	PMID:21378380	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0004322	PMID:21378380	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0004442	PMID:21378380	PCS		1/2			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0001394	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0008070	PMID:21378380	PCS		1/2			P	HPO:skoehler[2013-08-10];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000958	OMIM:614099	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000774	PMID:21378380	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000256	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0001821	PMID:21378380	PCS		2/2			P	HPO:skoehler[2013-08-10];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000973	OMIM:614099	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0002213	OMIM:614099	TAS					P	HPO:skoehler[2013-08-10]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000232	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0010714	PMID:21378380	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0001382	PMID:21378380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0004691	PMID:21378380	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000090	PMID:21378380	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0100259	PMID:21378380	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000968	OMIM:614099	IEA					P	HPO:skoehler[2015-01-14]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000506	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000007	PMID:21378380	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0004969	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000268	OMIM:614099	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0002007	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0001852	PMID:21378380	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000685	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000347	PMID:21378380	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0001799	PMID:21378380	PCS		2/2			P	HPO:skoehler[2013-08-10];HPO:probinson[2023-03-29]
OMIM:614099	Cranioectodermal dysplasia 3		HP:0000687	PMID:21378380	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0002960	PMID:21206088	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0002014	PMID:21206088	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0001045	PMID:21206088	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0002232	PMID:21206088	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0020072	PMID:21206088	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0001890	PMID:21206088	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0003593	PMID:21206088	PCS		1/2			C	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0002240	PMID:21206088	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0032170	PMID:21206088	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0032061	PMID:21206088	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0009098	PMID:21206088	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0001508	PMID:21206088	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0011463	PMID:21206088	PCS		1/2			C	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0000007	PMID:21206088	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0002716	PMID:21206088	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0000403	PMID:21206088	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0002205	PMID:21206088	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0001744	PMID:21206088	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615387	Immunodeficiency 7, TCR-alpha/beta deficient		HP:0001875	PMID:21206088	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0003577	PMID:11286616	PCS		5/5			C	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0001030	PMID:11286616	PCS		0/5			P	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0008066	PMID:11286616	PCS		0/5			P	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0040189	PMID:11286616	PCS		0/5			P	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0045059	PMID:11286616	PCS		5/5			P	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0009775	PMID:11286616	PCS		2/5			P	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0032541	PMID:11286616	PCS		5/5			P	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0000982	PMID:11286616	PCS		5/5			P	HPO:probinson[2023-03-25]
OMIM:146590	Ichthyosis hystrix, Curth-Macklin type		HP:0000006	PMID:11286616	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0002078	PMID:26812546	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0001321	PMID:26812546	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0031936	PMID:26812546	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0001310	PMID:26812546	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0003487	PMID:26812546	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0001260	PMID:26812546	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0001263	PMID:26812546	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0003680	PMID:26812546	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0001251	OMIM:617584	TAS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0003593	PMID:26812546	PCS		2/2			C	HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0000007	PMID:26812546	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0000666	PMID:26812546	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25		HP:0001348	PMID:26812546	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0006934	OMIM:183800	IEA					P	HPO:skoehler[2015-01-27]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0000486	OMIM:183800	IEA					P	HPO:iea[2009-02-17]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0004058	OMIM:183800	IEA					P	HPO:iea[2009-02-17]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0000518	OMIM:183800	IEA					P	HPO:iea[2009-02-17]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0000639	PMID:9450888	PCS					P	HPO:probinson[2009-02-17]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0001839	OMIM:183800	IEA					P	HPO:iea[2009-02-17]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0001171	OMIM:183800	IEA					P	HPO:iea[2009-02-17]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0000488	OMIM:183800	TAS					P	HPO:skoehler[2015-07-26]
OMIM:183800	Split-Hand with congenital nystagmus, fundal changes, and cataracts		HP:0000006	OMIM:183800	IEA					I	HPO:iea[2009-02-17]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0008969	OMIM:108600	IEA					P	HPO:iea[2009-02-17]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0002015	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0003621	PMID:22958904	PCS					C	HPO:probinson[2022-09-29]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0002354	OMIM:108600	IEA					P	HPO:iea[2009-02-17]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0002497	OMIM:108600	IEA					P	HPO:iea[2009-02-17]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0000496	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0001332	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0001288	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0001761	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0001260	OMIM:108600	IEA					P	HPO:iea[2009-02-17]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0000605	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0011462	PMID:22958904	PCS					C	HPO:probinson[2022-09-29]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0000508	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0000514	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0001258	OMIM:108600	IEA					P	HPO:iea[2009-02-17]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0000006	PMID:22958904	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:108600	Spastic ataxia 1, autosomal dominant		HP:0001347	OMIM:108600	TAS					P	HPO:skoehler[2014-07-11]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0004763	OMIM:616117	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0001695	OMIM:616117	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0001692	PMID:24925317	IEA					P	HPO:probinson[2015-03-28]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0005110	OMIM:616117	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0011711	PMID:24925317	IEA					P	HPO:probinson[2015-03-28]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0011712	OMIM:616117	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0005184	OMIM:616117	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0006682	OMIM:616117	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0001635	OMIM:616117	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0004749	OMIM:616117	TAS					P	HPO:skoehler[2015-08-16]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0001649	OMIM:616117	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0000006	PMID:24925317	IEA					I	HPO:probinson[2015-03-28]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0001644	PMID:24925317	IEA					P	HPO:probinson[2015-03-28]
OMIM:616117	Cardiac conduction disease with or without dilated cardiomyopathy		HP:0001688	OMIM:616117	IEA					P	HPO:skoehler[2019-09-07]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0002421	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0003577	PMID:27159321	IEA		1/5			C	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0001332	PMID:27159321	PCS		2/5			P	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0001371	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0001252	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0012707	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0003593	PMID:27159321	PCS		2/5			C	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0001251	PMID:27159321	PCS		2/3			P	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0001290	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0012402	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0000737	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0011463	PMID:22972948;PMID:27159321	PCS		3/6			C	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0008872	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0008314	PMID:22972948	IEA		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0025336	PMID:27159321	PCS		1/5			P	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0002415	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0001347	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0008936	PMID:27159321	PCS		4/5			P	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0000252	PMID:27159321	PCS		1/5			P	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0000750	PMID:27159321	PCS		1/5			P	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0031936	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0003542	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0002376	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0025335	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0002373	PMID:27159321	PCS		1/5			P	HPO:probinson[2022-04-04]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0002151	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0030890	PMID:26925370	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0000007	PMID:22972948	PCS					I	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0002527	PMID:22972948	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:619224	Mitochondrial complex II deficiency, nuclear type 4		HP:0001257	PMID:27159321	PCS		4/5			P	HPO:probinson[2022-04-04]
OMIM:600775	Craniosynostosis 4		HP:0000750	PMID:26097063	PCS		1/2			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0004443	PMID:23354439	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0004442	PMID:23354439	PCS		7/8			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0004440	PMID:23354439	PCS		3/8			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0000272	PMID:23354439;PMID:26097063	PCS		5/28			P	HPO:probinson[2022-03-07];HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0003593	PMID:26097063	PCS		1/2			C	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0011755	PMID:26097063	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0011325	PMID:26097063	PCS		1/2			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0011800	PMID:23354439	PCS		4/26			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0011318	PMID:26097063	PCS		1/2			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0005280	PMID:26097063	PCS		1/2			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0031987	PMID:23354439	PCS		5/26			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0000609	PMID:26097063	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0011463	PMID:26097063	PCS		1/2			C	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0007099	PMID:23354439	PCS		4/26			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0011220	PMID:23354439	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0011330	PMID:23354439;PMID:26097063	PCS		2/10			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0000316	PMID:23354439;PMID:26097063	PCS		16/28			P	HPO:probinson[2022-03-07];HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0002516	PMID:23354439	PCS		9/26			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0000256	PMID:23354439	PCS		7/26			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0000278	PMID:26097063	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0000520	PMID:23354439;PMID:26097063	PCS		7/28			P	HPO:probinson[2022-03-07]
OMIM:600775	Craniosynostosis 4		HP:0000006	PMID:23354439	PCS					I	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0006528	PMID:22608502	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002582	PMID:22608502	PCS		1/5			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002583	PMID:22608502	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001890	PMID:22981790;PMID:22608502;PMID:26206937	PCS		8/15			P	HPO:probinson[2020-11-27];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27];HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0410252	PMID:22981790	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0100651	PMID:26206937	PCS		3/9			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0032140	PMID:26206937	PCS		6/8			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001508	PMID:22608502	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002719	PMID:22981790	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0100646	PMID:26206937	PCS		1/9			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0100806	PMID:22981790	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002716	PMID:22608502	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0006532	PMID:22721650	PCS		1/5			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0000554	PMID:26206937	PCS		2/9			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001744	PMID:22981790;PMID:26206937	PCS		9/10			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001369	PMID:22608502;PMID:26206937	PCS		2/14			P	HPO:probinson[2020-11-27];HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0004315	PMID:22608502;PMID:26206937	PCS		10/14			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002850	PMID:22608502	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001045	PMID:26206937	PCS		1/9			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002037	PMID:22608502	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0005523	PMID:22721650	PCS		1/5		HP:0033185	P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0030388	PMID:22608502	PCS		4/4			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002099	PMID:22608502	PCS	HP:0011463	1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002110	PMID:22608502	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0012219	PMID:22981790	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002090	PMID:22608502	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0011108	PMID:22608502	PCS		1/5			P	HPO:skoehler[2012-11-20];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0010976	PMID:26206937	PCS		5/9			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0100759	PMID:22608502	PCS		1/5			P	HPO:skoehler[2012-11-20];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0000509	PMID:22608502	PCS		1/5			P	HPO:skoehler[2012-11-20];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0011473	PMID:22721650;PMID:22981790	PCS		4/6			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0025526	PMID:26206937	PCS		2/9			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0000007	PMID:22608502	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0000821	PMID:22608502	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0000403	PMID:22721650;PMID:22608502	PCS		3/10			P	HPO:skoehler[2012-11-20];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0008940	PMID:22981790	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001973	PMID:22721650;PMID:22608502;PMID:26206937	PCS		10/19			P	HPO:probinson[2020-11-27];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002205	PMID:22608502	PCS		5/5			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001510	PMID:22981790;PMID:22608502	PCS		2/6			P	HPO:probinson[2020-11-27];HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001873	PMID:22981790	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002720	PMID:22608502;PMID:26206937	PCS		7/9			P	HPO:probinson[2020-11-27];HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0001876	PMID:22721650	PCS		1/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002665	PMID:26206937	PCS		1/9			P	HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002028	PMID:22721650;PMID:22981790;PMID:22608502	PCS		7/11			P	HPO:probinson[2020-11-27];HPO:skoehler[2013-05-29];HPO:probinson[2020-11-27]
OMIM:614700	Immunodeficiency, common variable, 8, with autoimmunity		HP:0002721	PMID:22608502	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-11-27]
OMIM:145700	Hypertrichosis universalis		HP:0004540	OMIM:145700	IEA					P	HPO:iea[2009-02-17]
OMIM:145700	Hypertrichosis universalis		HP:0010730	OMIM:145700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:145700	Hypertrichosis universalis		HP:0000006	OMIM:145700	IEA					I	HPO:iea[2009-02-17]
OMIM:615378	Atrial fibrillation, familial, 14		HP:0003596	PMID:19808477	PCS		2/2			C	HPO:probinson[2022-07-10]
OMIM:615378	Atrial fibrillation, familial, 14		HP:0012251	PMID:19808477	PCS		2/2			P	HPO:probinson[2015-05-10]
OMIM:615378	Atrial fibrillation, familial, 14		HP:0000822	PMID:19808477	PCS		1/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-07-10]
OMIM:615378	Atrial fibrillation, familial, 14		HP:0004757	PMID:19808477	PCS		2/2			P	HPO:probinson[2015-05-10]
OMIM:615378	Atrial fibrillation, familial, 14		HP:0000006	PMID:19808477	PCS					I	HPO:probinson[2015-05-10]
OMIM:615378	Atrial fibrillation, familial, 14		HP:0012248	PMID:19808477	PCS		1/2			P	HPO:probinson[2015-05-10]
OMIM:188000	Thrombocytopenia 2		HP:0034010	PMID:10891439	PCS		2/2			P	HPO:probinson[2021-10-03]
OMIM:188000	Thrombocytopenia 2		HP:0011876	PMID:10891439	PCS		0/13			P	HPO:probinson[2021-08-27];HPO:probinson[2024-03-08]
OMIM:188000	Thrombocytopenia 2		HP:0000978	PMID:10891439	PCS		20/20			P	HPO:probinson[2021-08-27];HPO:iea[2009-02-17];HPO:probinson[2021-08-27]
OMIM:188000	Thrombocytopenia 2		HP:0001873	PMID:10891439;PMID:21211618	PCS		48/48			P	HPO:probinson[2021-08-27];HPO:iea[2009-02-17];HPO:probinson[2021-08-27]
OMIM:188000	Thrombocytopenia 2		HP:0000006	PMID:21211618	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-08-27]
OMIM:188000	Thrombocytopenia 2		HP:0012524	PMID:10891439	PCS		0/13			P	HPO:probinson[2021-08-27];HPO:probinson[2024-03-08]
OMIM:188000	Thrombocytopenia 2		HP:0001974	PMID:10891439	PCS					P	HPO:probinson[2021-08-27]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000341	OMIM:614066	TAS					P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001276	PMID:21620353	PCS	HP:0011463	3/3			P	HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0003577	OMIM:614066	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0002540	PMID:21620353	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0004322	OMIM:614066	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001332	OMIM:614066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001250	OMIM:614066	TAS					P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001371	OMIM:614066	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0008807	OMIM:614066	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000280	OMIM:614066	TAS					P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0100962	PMID:21620353	PCS		2/3			P	HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0002816	OMIM:614066	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000414	OMIM:614066	TAS					P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0002518	OMIM:614066	TAS					P	HPO:skoehler[2013-06-05]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0002515	OMIM:614066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0002119	OMIM:614066	TAS					P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000218	OMIM:614066	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001763	OMIM:614066	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001347	PMID:21620353	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000154	OMIM:614066	TAS					P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000252	PMID:21620353	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000431	OMIM:614066	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001762	OMIM:614066	TAS		HP:0040283			P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000750	OMIM:614066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0002079	OMIM:614066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0003487	PMID:21620353	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0031936	PMID:21620353	PCS		3/3			P	HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001260	OMIM:614066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001263	OMIM:614066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000007	PMID:21620353	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001319	PMID:21620353	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0025502	PMID:21620353	PCS		2/3			P	HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0002307	PMID:21620353	PCS		1/3			P	HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001258	OMIM:614066	IEA					P	HPO:skoehler[2015-01-27]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0001257	PMID:21620353	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0000322	OMIM:614066	TAS					P	HPO:skoehler[2015-10-16]
OMIM:614066	Spastic paraplegia 47, autosomal recessive		HP:0003677	OMIM:614066	TAS					C	HPO:skoehler[2012-10-17]
OMIM:619542	King-Denborough syndrome		HP:0030799	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0002047	PMID:18765655;PMID:21514828;PMID:27918309	PCS		2/6			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0003236	PMID:18765655;PMID:21514828	PCS		3/5			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0002002	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0004322	PMID:21514828	PCS		2/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001252	PMID:18765655;PMID:21514828;PMID:27918309	PCS		5/6			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0100295	PMID:21514828	PCS		4/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001270	PMID:21514828	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0030319	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001508	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001629	PMID:27918309	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0011463	PMID:21514828	PCS		1/4			C	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0002938	PMID:18765655;PMID:21514828	PCS		4/5			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0011461	PMID:18765655	PCS		1/1			C	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000316	PMID:21514828	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0009765	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000218	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0003803	PMID:18765655;PMID:21514828	PCS		3/5			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000455	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0003701	PMID:18765655;PMID:21514828	PCS		5/5			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0003789	PMID:21514828	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001488	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001623	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0002058	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0002751	PMID:21514828	PCS		4/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000494	PMID:21514828	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0003687	PMID:21514828	PCS		2/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0003621	PMID:21514828	PCS		3/4			C	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0002650	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0031936	PMID:27918309	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001382	PMID:21514828	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000470	PMID:21514828	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0011800	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000508	PMID:21514828;PMID:27918309	PCS		4/5			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0003738	PMID:21514828	PCS		1/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0001558	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0002942	PMID:18765655	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000465	PMID:18765655;PMID:21514828	PCS		3/5			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0008689	PMID:27918309	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000006	PMID:18765655	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2022-01-23]
OMIM:619542	King-Denborough syndrome		HP:0000369	PMID:21514828	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:619542	King-Denborough syndrome		HP:0000028	PMID:21514828	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:141200	Hematuria, benign familial		HP:0000790	OMIM:141200	IEA					P	HPO:iea[2009-02-17]
OMIM:141200	Hematuria, benign familial		HP:0003680	OMIM:141200	TAS					C	HPO:skoehler[2012-10-17]
OMIM:141200	Hematuria, benign familial		HP:0012577	OMIM:141200	TAS					P	HPO:skoehler[2014-01-28]
OMIM:141200	Hematuria, benign familial		HP:0000006	OMIM:141200	IEA					I	HPO:iea[2009-02-17]
OMIM:618884	Proteinuria, chronic benign		HP:0000083	PMID:31613795	PCS		0/39			P	HPO:probinson[2020-07-11];HPO:probinson[2022-06-11]
OMIM:618884	Proteinuria, chronic benign		HP:0012592	PMID:31613795	PCS	HP:0011463	39/39			P	HPO:probinson[2020-07-11];HPO:probinson[2022-06-11]
OMIM:618884	Proteinuria, chronic benign		HP:0000007	PMID:31613795	PCS					I	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618884	Proteinuria, chronic benign		HP:0000093	PMID:31613795	PCS	HP:0011463	39/39			P	HPO:probinson[2020-07-11];HPO:probinson[2022-06-11]
OMIM:300582	Short stature, idiopathic familial		HP:0004322	PMID:19578035	PCS					P	HPO:probinson[2013-02-17]
OMIM:300582	Short stature, idiopathic familial		HP:0001417	PMID:19578035	PCS					I	HPO:probinson[2013-01-09]
OMIM:618648	Immunodeficiency 65, susceptibility to viral infections		HP:0000230	PMID:30826365	PCS					P	HPO:probinson[2020-07-19]
OMIM:618648	Immunodeficiency 65, susceptibility to viral infections		HP:0010280	PMID:30826365	PCS					P	HPO:probinson[2020-07-19]
OMIM:618648	Immunodeficiency 65, susceptibility to viral infections		HP:0002110	PMID:30826365	PCS					P	HPO:probinson[2020-07-19]
OMIM:618648	Immunodeficiency 65, susceptibility to viral infections		HP:0000007	PMID:30826365	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:618648	Immunodeficiency 65, susceptibility to viral infections		HP:0031123	PMID:30826365	PCS					P	HPO:probinson[2020-07-19]
OMIM:618648	Immunodeficiency 65, susceptibility to viral infections		HP:0004429	PMID:30826365	PCS	HP:0003593				P	HPO:probinson[2020-07-19]
OMIM:601319	Odontomicronychial dysplasia		HP:0008383	OMIM:601319	PCS					P	HPO:probinson[2009-02-17]
OMIM:601319	Odontomicronychial dysplasia		HP:0001816	OMIM:601319	PCS					P	HPO:probinson[2012-03-03]
OMIM:601319	Odontomicronychial dysplasia		HP:0000007	OMIM:601319	IEA					I	HPO:iea[2009-02-17]
OMIM:601319	Odontomicronychial dysplasia		HP:0006337	OMIM:601319	IEA					P	HPO:iea[2009-02-17]
OMIM:601319	Odontomicronychial dysplasia		HP:0001799	OMIM:601319	PCS					P	HPO:probinson[2012-03-03]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000341	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001276	PMID:34314705	PCS		2/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000483	PMID:34314705	PCS		4/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000343	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0002265	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000486	PMID:34314705	PCS		7/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0002540	PMID:34314705	PCS		3/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0002188	PMID:34314705	PCS				HP:0012825	P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000540	PMID:34314705	PCS		4/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001250	PMID:34314705	PCS		6/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001252	PMID:34314705	PCS		11/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0003593	PMID:34314705	PCS					C	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001251	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000280	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001508	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0002119	PMID:34314705	PCS				HP:0012825	P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000278	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001249	PMID:34314705	PCS		9/9			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0002058	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000252	PMID:34314705	PCS		5/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000750	PMID:34314705	PCS		15/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000431	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001344	PMID:34314705	PCS		4/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000232	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001321	PMID:34314705	PCS		3/13			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0011968	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001263	PMID:34314705	PCS		15/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000729	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000426	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000322	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0007018	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000006	PMID:34314705	PCS					I	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0000545	PMID:34314705	PCS		4/15			P	HPO:probinson[2022-01-23]
OMIM:619556	Intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies		HP:0001337	PMID:34314705	PCS					P	HPO:probinson[2022-01-23]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0001298	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0001276	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0008936	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0002521	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0006956	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0000252	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0002079	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0002033	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0032794	PMID:29090338	PCS	HP:0003593	1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0012736	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0012469	PMID:29090338	PCS	HP:0003593	1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0011471	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0007281	PMID:29090338	PCS	HP:0003593	1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0000609	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0032792	PMID:29090338	PCS	HP:0003593	1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0011153	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0000007	PMID:29090338	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0025404	PMID:29090338	PCS	HP:0003623	1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0001257	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618890	Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity		HP:0001623	PMID:29090338	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0001892	PMID:34608437;PMID:11455388	PCS		11/11			P	HPO:probinson[2013-08-10];HPO:probinson[2020-06-28];HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0001022	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0006934	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0003621	PMID:34608437	PCS		1/1			C	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0005599	PMID:11455388	PCS				HP:0012825	P	HPO:probinson[2020-06-28]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0003540	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0001010	PMID:11455388	PCS				HP:0012825	P	HPO:probinson[2020-06-28]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0012530	PMID:11455388	PCS					P	HPO:probinson[2020-06-28]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0000639	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0000007	PMID:11455388	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-06-28]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0007663	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0000978	PMID:34608437	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0000505	PMID:11455388	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-06-28]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0000565	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0004406	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0000666	PMID:11455388	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-06-28]
OMIM:614072	Hermansky-Pudlak syndrome 3		HP:0000225	PMID:34608437	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:220120	D-glyceric aciduria		HP:0002069	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001298	PMID:1909405;PMID:20949620	PCS		11/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25];HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0002521	OMIM:220120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220120	D-glyceric aciduria		HP:0002188	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:6000371	PMID:1909405	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0003355	OMIM:220120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:220120	D-glyceric aciduria		HP:0002266	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:6000372	PMID:1909405	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0002120	PMID:20949620	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001250	PMID:1909405	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0001252	PMID:20949620	PCS		3/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0002020	PMID:20949620	PCS		2/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0003593	PMID:1909405	PCS		1/1			C	HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0001508	PMID:20949620	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0100703	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0000954	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001943	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001643	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001348	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001249	PMID:20949620	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001942	PMID:20949620	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001347	OMIM:220120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220120	D-glyceric aciduria		HP:0003623	PMID:20949620	PCS		3/3			C	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0008936	PMID:1909405	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:220120	D-glyceric aciduria		HP:0002179	PMID:1909405	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:220120	D-glyceric aciduria		HP:0034706	PMID:2537226	PCS		1/1			P	HPO:probinson[2023-06-05]
OMIM:220120	D-glyceric aciduria		HP:0000252	PMID:1909405;PMID:20949620	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25];HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0000054	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0002510	PMID:1909405	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:220120	D-glyceric aciduria		HP:0002133	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001662	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0000490	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001263	PMID:1909405;PMID:20949620	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25];HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0000609	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0034353	PMID:1909405	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0000407	OMIM:220120	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:220120	D-glyceric aciduria		HP:0008288	OMIM:220120	IEA					P	HPO:iea[2009-02-17]
OMIM:220120	D-glyceric aciduria		HP:0000007	PMID:20949620	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001319	OMIM:220120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220120	D-glyceric aciduria		HP:0001510	PMID:1909405;PMID:20949620	PCS		11/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25];HPO:probinson[2024-02-27]
OMIM:220120	D-glyceric aciduria		HP:0001257	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0002643	PMID:20949620	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:220120	D-glyceric aciduria		HP:0001336	OMIM:220120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614714	Porokeratosis 7, multiple types		HP:0001036	PMID:22983302	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-13]
OMIM:614714	Porokeratosis 7, multiple types		HP:0200044	PMID:22983302	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2021-07-13]
OMIM:614714	Porokeratosis 7, multiple types		HP:0000006	PMID:22983302	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2021-07-13]
OMIM:181030	Salivary gland adenoma, pleomorphic		HP:0001442	OMIM:181030	TAS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:181030	Salivary gland adenoma, pleomorphic		HP:0100684	OMIM:181030	TAS					P	HPO:iea[2015-05-12]
OMIM:181030	Salivary gland adenoma, pleomorphic		HP:0000006	OMIM:181030	TAS					I	HPO:iea[2009-02-17]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0003202	PMID:11891683	PCS					P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0003687	PMID:23455423	PCS		2/2			P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0003236	PMID:11891683	PCS					P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0002145	PMID:11891683	PCS					P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0003198	PMID:23455423	PCS		5/5			P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0003155	PMID:11891683	PCS					P	HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0100295	PMID:23455423	PCS					P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0034159	PMID:23455423	PCS		5/5			P	HPO:probinson[2022-04-15]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0000708	PMID:23455423	PCS		1/5			P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0100543	PMID:23455423	PCS		2/5			P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0100614	PMID:11891683	PCS					P	HPO:skoehler[2015-08-29];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0003805	PMID:23455423	PCS		2/2			P	HPO:probinson[2022-02-09];HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0001324	PMID:23455423	PCS					P	HPO:probinson[2022-02-09]
OMIM:615422	Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2		HP:0000006	PMID:23455423	PCS					I	HPO:probinson[2022-02-09]
OMIM:204900	Amyloidosis, cutaneous bullous		HP:0011034	OMIM:204900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:204900	Amyloidosis, cutaneous bullous		HP:0000007	OMIM:204900	IEA					I	HPO:iea[2009-02-17]
OMIM:204900	Amyloidosis, cutaneous bullous		HP:0000951	OMIM:204900	IEA					P	HPO:iea[2009-02-17]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0000011	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0003577	PMID:33568816	PCS		1/1			C	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0000252	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0000010	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0001770	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0000750	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0030884	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0002365	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0001382	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0001252	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0001290	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0012642	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0032988	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0033977	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-07-16]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0009460	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0031260	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0001508	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0011167	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0001537	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0000007	PMID:33568816	PCS					I	HPO:probinson[2021-05-18];HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0000126	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619218	ENDOVE syndrome, limb-brain type		HP:0002754	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0001287	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0002014	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0005403	OMIM:601457	IEA				HP:0012828	P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0000265	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0004430	OMIM:601457	TAS					P	HPO:probinson[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0002090	OMIM:601457	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0010976	OMIM:601457	TAS				HP:0012828	P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0005390	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0040334	OMIM:601457	IEA					P	HPO:skoehler[2019-04-18]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0001508	OMIM:601457	TAS					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0000509	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0000007	OMIM:601457	IEA					I	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0008866	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0000388	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0001369	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:601457	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive		HP:0003139	OMIM:601457	IEA					P	HPO:iea[2009-02-17]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0002465	OMIM:618106	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000486	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0004322	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000023	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001250	PMID:29688601	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0010808	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001252	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0011937	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0003593	PMID:29688601	PCS					C	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0012471	PMID:29688601	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000954	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000316	PMID:29688601	PCS		2/5			P	HPO:nvasilevsky[2019-02-26];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000678	PMID:29688601	PCS		1/5			P	HPO:nvasilevsky[2019-02-26];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000218	PMID:29688601	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000455	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000358	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001249	PMID:29688601	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001348	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000154	PMID:29688601	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000176	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0002311	PMID:29688601	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000297	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0008936	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000252	OMIM:618106	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0007429	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000494	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000431	PMID:29688601	PCS		1/5			P	HPO:nvasilevsky[2019-02-26];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000750	PMID:29688601	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000331	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0031936	PMID:29688601	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001382	PMID:29688601	PCS		1/5			P	HPO:nvasilevsky[2019-02-26];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0011968	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001263	PMID:29688601	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0003186	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000307	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0002527	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001357	PMID:29688601	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000400	OMIM:618106	TAS					P	HPO:nvasilevsky[2019-02-26]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000006	PMID:29688601	PCS					I	HPO:nvasilevsky[2019-02-26];HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0001611	PMID:29688601	PCS		1/5			P	HPO:probinson[2022-06-01]
OMIM:618106	Intellectual developmental disorder, autosomal dominant 58		HP:0000324	PMID:29688601	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-01];HPO:probinson[2022-06-01]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0003577	PMID:27463701	PCS		2/2			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0002015	PMID:27463701	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0000252	PMID:27463701	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0002188	PMID:27463701;PMID:27414745	PCS		2/3			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0002079	PMID:27414745	PCS		1/1			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0011968	PMID:27463701	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0002033	PMID:27463701	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0001252	PMID:27463701;PMID:27414745	PCS		3/3			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0001263	PMID:27463701	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0002072	PMID:27463701	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0031146	PMID:27463701	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0100704	PMID:27463701	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0000508	PMID:27463701	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0006980	PMID:27414745	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0020221	PMID:27414745	PCS	HP:0003623	1/1			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0001305	PMID:27414745	PCS		1/1			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0000543	PMID:27463701	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0002305	PMID:27463701	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0002104	PMID:27463701	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0000006	PMID:27463701	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0000666	PMID:27463701	PCS		1/2			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0001336	PMID:27463701;PMID:27414745	PCS		3/3			P	HPO:probinson[2023-01-30];HPO:skoehler[2018-10-08];HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0003557	PMID:27463701	PCS		1/1			P	HPO:probinson[2023-01-30]
OMIM:617235	Myoclonus, intractable, neonatal		HP:0003623	PMID:27414745	PCS		1/1			C	HPO:probinson[2023-01-30]
OMIM:620499	Spermatogenic failure 86		HP:0003251	PMID:32923619	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:620499	Spermatogenic failure 86		HP:0011462	PMID:34727571;PMID:32923619	PCS		3/3			C	HPO:probinson[2024-02-11]
OMIM:620499	Spermatogenic failure 86		HP:0000007	PMID:32923619	PCS					I	HPO:probinson[2024-02-11]
OMIM:620499	Spermatogenic failure 86		HP:0012869	PMID:34727571	PCS		1/1			P	HPO:probinson[2024-02-11]
OMIM:620499	Spermatogenic failure 86		HP:6000501	PMID:32923619	PCS		2/2			P	HPO:probinson[2024-04-04]
OMIM:620499	Spermatogenic failure 86		HP:0034913	PMID:34727571	PCS		1/1			P	HPO:probinson[2024-02-11]
OMIM:620499	Spermatogenic failure 86		HP:0012865	PMID:32923619	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:618660	Hemolytic anemia due to glutathione reductase deficiency		HP:0000518	PMID:17185460	PCS	HP:0003581	3/3			P	HPO:probinson[2020-03-28]
OMIM:618660	Hemolytic anemia due to glutathione reductase deficiency		HP:0002904	PMID:17185460	PCS					P	HPO:probinson[2020-03-28]
OMIM:618660	Hemolytic anemia due to glutathione reductase deficiency		HP:0000007	PMID:17185460	PCS					I	HPO:probinson[2020-03-28];HPO:probinson[2020-03-28]
OMIM:618660	Hemolytic anemia due to glutathione reductase deficiency		HP:6000525	PMID:17185460	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:618660	Hemolytic anemia due to glutathione reductase deficiency		HP:0004814	PMID:17185460	PCS					P	HPO:probinson[2020-03-28]
OMIM:601331	Renal dysplasia, cystic, susceptibility to		HP:0000110	OMIM:601331	TAS					P	HPO:probinson[2009-02-17]
OMIM:601331	Renal dysplasia, cystic, susceptibility to		HP:0000076	OMIM:601331	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:601331	Renal dysplasia, cystic, susceptibility to		HP:0030674	PMID:23374899	PCS					C	HPO:probinson[2020-07-17]
OMIM:601331	Renal dysplasia, cystic, susceptibility to		HP:0000083	OMIM:601331	TAS					P	HPO:probinson[2014-01-18]
OMIM:601331	Renal dysplasia, cystic, susceptibility to		HP:0004719	OMIM:601331	TAS					P	HPO:skoehler[2013-04-18]
OMIM:601331	Renal dysplasia, cystic, susceptibility to		HP:0000800	OMIM:601331	TAS					P	HPO:probinson[2014-01-18]
OMIM:601331	Renal dysplasia, cystic, susceptibility to		HP:0000006	OMIM:601331	TAS					I	HPO:skoehler[2012-10-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0004963	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0007759	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0000486	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0001640	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0001761	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0001250	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0002240	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0004382	PMID:1333717	PCS					P	HPO:probinson[2017-12-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0004380	OMIM:231005	PCS					P	HPO:probinson[2017-12-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0001718	OMIM:231005	IEA					P	HPO:skoehler[2018-10-08]
OMIM:231005	Gaucher disease, type IIIC		HP:0000007	OMIM:231005	IEA					I	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0000238	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0000623	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0007885	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0007975	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0000666	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0001744	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:231005	Gaucher disease, type IIIC		HP:0001876	OMIM:231005	IEA					P	HPO:iea[2009-02-17]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0003676	PMID:23883380	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0003621	PMID:23883380	PCS		1/7			C	HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0003596	PMID:23883380	PCS		1/7			C	HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0011705	PMID:23883380	PCS		1/9			P	HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0004890	PMID:23883380	PCS		7/9			P	HPO:skoehler[2015-08-28];HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0011712	PMID:23883380	PCS		2/9			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0002092	PMID:23883380	PCS		7/9			P	HPO:skoehler[2015-08-28];HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0033424	PMID:23883380	PCS		5/5			P	HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0001907	PMID:23883380	PCS		0/9			P	HPO:skoehler[2015-08-28];HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0011462	PMID:23883380	PCS		5/7			C	HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0004749	PMID:23883380	PCS		1/9			P	HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0000006	PMID:23883380	PCS					I	HPO:skoehler[2015-08-28];HPO:probinson[2022-03-20]
OMIM:615344	Pulmonary hypertension, primary, 4		HP:0005317	PMID:23883380	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-20]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000582	PMID:24462883	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000463	PMID:24462883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000023	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000089	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0001250	PMID:24462883	PCS		0/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0003396	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000160	OMIM:613735	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0001274	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0001252	PMID:24462883	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0003196	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000283	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0003593	PMID:24462883	PCS		1/1			C	HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0010862	PMID:24462883	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0100543	OMIM:613735	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0001508	PMID:24462883	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000337	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000219	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0002119	PMID:24462883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0003745	OMIM:613735	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000256	PMID:24462883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0001249	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000396	PMID:24462883	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000076	OMIM:613735	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0002079	PMID:24462883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000331	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0001263	PMID:24462883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0002194	PMID:24462883	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0007099	PMID:24462883	PCS		0/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0011330	PMID:24462883	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000965	PMID:24462883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000006	PMID:24462883	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000369	OMIM:613735	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613735	Brain malformations with or without urinary tract defects		HP:0000126	PMID:24462883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0002421	PMID:23768512	PCS		2/8			P	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0003577	PMID:23768512	PCS		3/8			C	HPO:skoehler[2013-10-06]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0003236	PMID:23768512	PCS		8/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0002540	PMID:23768512	PCS		2/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001250	PMID:23768512	PCS		4/8			P	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0003551	PMID:23768512	PCS		1/8			P	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001252	PMID:23768512	PCS		2/8			P	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001251	PMID:23768512	PCS		1/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0003593	PMID:23768512	PCS		2/8			C	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0012110	PMID:23768512	PCS		1/7			P	HPO:skoehler[2014-09-21];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0000518	PMID:23768512	PCS		3/8			P	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0011463	PMID:23768512	PCS		2/8			C	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001324	PMID:23768512	PCS		8/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001249	PMID:23768512	PCS		7/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0003623	PMID:23768512	PCS		1/8			C	HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001562	PMID:23768512	PCS		1/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0000175	PMID:23768512	PCS		1/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0000252	PMID:23768512	PCS		4/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001344	PMID:23768512	PCS		1/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001321	PMID:23768512	PCS		3/7			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0011968	PMID:23768512	PCS		2/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0030046	PMID:23768512	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001263	PMID:23768512	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0003560	PMID:23768512	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0000407	PMID:23768512	PCS		1/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0000007	PMID:23768512	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615350	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14		HP:0001558	PMID:23768512	PCS		3/8			P	HPO:probinson[2023-05-17]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0002069	OMIM:613721	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0002487	PMID:15028761	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0002510	OMIM:613721	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0002133	OMIM:613721	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0002283	PMID:15028761	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0001263	OMIM:613721	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0003593	OMIM:613721	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0011344	PMID:15028761	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0011463	PMID:15028761	PCS		1/1			C	HPO:probinson[2023-04-02]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0000717	PMID:15028761	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0007334	PMID:15028761	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0200134	PMID:15028761	PCS		1/1			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-04-02]
OMIM:613721	Epileptic encephalopathy, early infantile, 11		HP:0000006	PMID:15028761	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-02]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0002267	PMID:26545878	PCS		1/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0001276	PMID:26545878	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0002169	PMID:26545878	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0004466	PMID:26545878	PCS		1/1			P	HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0002188	PMID:26545878	PCS		6/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0001251	PMID:26545878	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0003593	PMID:26545878	PCS		6/6			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0002061	PMID:26545878	PCS		3/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0001508	PMID:26545878	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0000639	PMID:26545878	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0000737	PMID:26545878	PCS		3/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0002518	PMID:26545878	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0002415	PMID:26545878	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0001347	PMID:26545878	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0008936	PMID:26545878	PCS		1/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0001344	PMID:26545878	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0002013	PMID:26545878	PCS		1/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0011968	PMID:26545878	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0001263	PMID:26545878	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0005484	PMID:26545878	PCS		5/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0034392	PMID:26545878	PCS		2/6			P	HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0000007	PMID:26545878	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0000648	PMID:26545878	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0000505	PMID:26545878	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:616881	Leukodystrophy, hypomyelinating, 13		HP:0001257	PMID:26545878	PCS		3/6			P	HPO:skoehler[2017-07-13]
OMIM:618674	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 5		HP:0005528	PMID:31488579	PCS	HP:0003581				P	HPO:probinson[2020-07-19]
OMIM:618674	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 5		HP:0002206	PMID:31488579	PCS	HP:0003581				P	HPO:probinson[2020-07-19]
OMIM:618674	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 5		HP:0031413	PMID:31488579	PCS					P	HPO:probinson[2020-07-19]
OMIM:618674	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 5		HP:0000006	PMID:31488579	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0007814	PMID:26294103	PCS		3/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0007737	PMID:26294103	PCS		2/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0003621	PMID:26294103	PCS		1/3			C	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0000662	OMIM:617547	IEA		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0004322	PMID:26294103	PCS		1/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0030856	PMID:26294103	PCS		3/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0100018	OMIM:617547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0011463	PMID:26294103	PCS		2/3			C	HPO:probinson[2023-02-16];HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0000613	OMIM:617547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0007663	PMID:26294103	PCS		2/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0000007	PMID:26294103	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0001956	PMID:26294103	PCS		1/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0000603	OMIM:617547	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0007787	PMID:26294103	PCS		1/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0007843	PMID:26294103	PCS		3/3			P	HPO:probinson[2023-02-16]
OMIM:617547	Retinal dystrophy with or without macular staphyloma		HP:0000556	PMID:26294103	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-16]
OMIM:139393	Neuropathy, inflammatory demyelinating		HP:0007131	PMID:12439896	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-24]
OMIM:139393	Neuropathy, inflammatory demyelinating		HP:0000006	PMID:12439896	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2020-07-24]
OMIM:618112	Spermatogenic failure 31		HP:0003251	PMID:30032984	PCS		5/5	MALE		P	HPO:probinson[2019-10-04]
OMIM:618112	Spermatogenic failure 31		HP:0003251	PMID:30298696	PCS		2/2			P	HPO:probinson[2019-10-04]
OMIM:618112	Spermatogenic failure 31		HP:0000007	PMID:30032984	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-10-04]
OMIM:618112	Spermatogenic failure 31		HP:0012869	PMID:30032984	PCS		5/5	MALE		P	HPO:probinson[2019-10-04]
OMIM:618112	Spermatogenic failure 31		HP:0012869	PMID:30298696	PCS		2/2			P	HPO:probinson[2019-10-04]
OMIM:614728	Seckel syndrome 6		HP:0003577	PMID:21983783	PCS		3/3			C	HPO:probinson[2022-11-02]
OMIM:614728	Seckel syndrome 6		HP:0000750	PMID:21983783	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-02]
OMIM:614728	Seckel syndrome 6		HP:0004322	PMID:21983783	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-02]
OMIM:614728	Seckel syndrome 6		HP:0011451	PMID:21983783	PCS	HP:0003577	3/3			P	HPO:probinson[2022-11-02]
OMIM:614728	Seckel syndrome 6		HP:0000007	PMID:21983783	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-11-02]
OMIM:614728	Seckel syndrome 6		HP:0001249	PMID:21983783	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-02]
OMIM:615436	Aortic aneurysm, familial thoracic 8		HP:0006702	PMID:23910461	PCS		1/31			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:615436	Aortic aneurysm, familial thoracic 8		HP:0005112	PMID:23910461	PCS		12/37			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-01]
OMIM:615436	Aortic aneurysm, familial thoracic 8		HP:0030882	PMID:23910461	PCS		1/31			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-01]
OMIM:615436	Aortic aneurysm, familial thoracic 8		HP:0003581	PMID:23910461	PCS					C	HPO:probinson[2021-05-01];HPO:probinson[2021-05-02]
OMIM:615436	Aortic aneurysm, familial thoracic 8		HP:0012499	PMID:23910461	PCS		6/31			P	HPO:probinson[2021-05-01]
OMIM:615436	Aortic aneurysm, familial thoracic 8		HP:0004933	PMID:23910461	PCS		11/31			P	HPO:probinson[2021-05-01]
OMIM:615436	Aortic aneurysm, familial thoracic 8		HP:0000006	PMID:23910461	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-01]
OMIM:603903	Sickle cell anemia		HP:0001297	OMIM:603903	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603903	Sickle cell anemia		HP:0001640	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0000083	OMIM:603903	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603903	Sickle cell anemia		HP:0000790	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0002240	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0001081	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0012418	OMIM:603903	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603903	Sickle cell anemia		HP:0034336	PMID:22084706	PCS					P	HPO:probinson[2022-10-06]
OMIM:603903	Sickle cell anemia		HP:0002718	OMIM:603903	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603903	Sickle cell anemia		HP:0001878	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0000822	OMIM:603903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603903	Sickle cell anemia		HP:0000007	OMIM:603903	TAS					I	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0008346	OMIM:603903	TAS					P	HPO:skoehler[2013-01-09]
OMIM:603903	Sickle cell anemia		HP:0200023	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0000488	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0000952	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0001744	OMIM:603903	TAS					P	HPO:skoehler[2013-02-21]
OMIM:603903	Sickle cell anemia		HP:0002027	OMIM:603903	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603903	Sickle cell anemia		HP:0001974	OMIM:603903	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603903	Sickle cell anemia		HP:0034280	PMID:27372866	PCS					P	HPO:probinson[2022-06-04]
OMIM:620102	Retinitis pigmentosa 95		HP:0001133	PMID:30377383	PCS		5/5			P	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0007737	PMID:30377383	PCS		4/6			P	HPO:probinson[2022-11-25];HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0003596	PMID:30377383	PCS		3/6			C	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0011463	PMID:30377383	PCS		1/6			C	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0000007	PMID:30377383	PCS					I	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0007663	PMID:30377383	PCS		6/6			P	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0030629	PMID:30377383	PCS		2/6			P	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0025710	PMID:30377383	PCS		2/6			C	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0000543	PMID:30377383	PCS		5/6			P	HPO:probinson[2022-11-25]
OMIM:620102	Retinitis pigmentosa 95		HP:0007843	PMID:30377383	PCS		6/6			P	HPO:probinson[2022-11-25]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0003445	OMIM:158590	IEA					P	HPO:iea[2009-02-17]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0009053	OMIM:158590	TAS					P	HPO:skoehler[2009-02-17]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0002460	OMIM:158590	IEA					P	HPO:iea[2009-02-17]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0003470	OMIM:158590	IEA					P	HPO:skoehler[2018-10-08]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0002601	OMIM:158590	IEA					P	HPO:iea[2009-02-17]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0000006	OMIM:158590	IEA					I	HPO:iea[2009-02-17]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0002522	OMIM:158590	IEA					P	HPO:iea[2009-02-17]
OMIM:158590	Neuronopathy, distal hereditary motor, type IIA		HP:0002600	OMIM:158590	TAS					P	HPO:skoehler[2013-03-27]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002069	PMID:28422131	PCS		3/3			P	HPO:probinson[2023-01-22];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002421	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002540	PMID:28422131	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000343	PMID:28422131	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000486	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002123	PMID:28422131	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002120	PMID:28422131	PCS		0/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0001250	PMID:28422131	PCS		3/3		HP:0031375	P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0001252	PMID:28422131	PCS		3/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0003593	PMID:28422131	PCS		3/3			C	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0032794	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002719	PMID:28422131	PCS		2/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000316	PMID:28422131	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0001845	PMID:28422131	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000414	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000219	PMID:28422131	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0001249	PMID:28422131	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002553	PMID:28422131	PCS		2/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000175	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0001344	PMID:28422131	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000574	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0031936	PMID:28422131	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0011968	PMID:28422131	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0002197	PMID:28422131	PCS		2/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0010818	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0001263	PMID:28422131	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0100021	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0011800	PMID:28422131	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0033258	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0011097	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0011198	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000007	PMID:26539891	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0200134	PMID:28422131	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617976	Epileptic encephalopathy, early infantile, 63		HP:0000405	PMID:28422131	PCS		1/3			P	HPO:probinson[2023-01-22]
OMIM:619783	Epidermolysis bullosa, junctional 2A, intermediate		HP:0033804	PMID:11810295	PCS		1/2			P	HPO:probinson[2022-05-11]
OMIM:619783	Epidermolysis bullosa, junctional 2A, intermediate		HP:0003577	PMID:11810295	PCS		2/2			C	HPO:probinson[2022-05-11]
OMIM:619783	Epidermolysis bullosa, junctional 2A, intermediate		HP:0008066	PMID:11810295	PCS		2/2			P	HPO:probinson[2022-05-11]
OMIM:619783	Epidermolysis bullosa, junctional 2A, intermediate		HP:0000007	PMID:11810295	PCS					I	HPO:probinson[2022-05-11]
OMIM:619783	Epidermolysis bullosa, junctional 2A, intermediate		HP:0200097	PMID:11810295	PCS		1/2			P	HPO:probinson[2022-05-11]
OMIM:267900	Retinal telangiectasia and hypogammaglobulinemia		HP:0002972	OMIM:267900	IEA					P	HPO:iea[2009-02-17]
OMIM:267900	Retinal telangiectasia and hypogammaglobulinemia		HP:0000007	OMIM:267900	IEA					I	HPO:iea[2009-02-17]
OMIM:267900	Retinal telangiectasia and hypogammaglobulinemia		HP:0007763	OMIM:267900	IEA					P	HPO:iea[2009-02-17]
OMIM:267900	Retinal telangiectasia and hypogammaglobulinemia		HP:0004315	OMIM:267900	IEA					P	HPO:iea[2009-02-17]
OMIM:615807	Seckel syndrome 8		HP:0002751	PMID:24389050	PCS		1/2		HP:0012828	P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0000252	PMID:24389050	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0003577	PMID:24389050	PCS		2/2			C	HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0004322	PMID:24389050	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0002176	PMID:24389050	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0000086	PMID:24389050	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0001263	PMID:24389050	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0000007	PMID:24389050	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0000444	PMID:24389050	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0001249	PMID:24389050	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:615807	Seckel syndrome 8		HP:0000347	PMID:24389050	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-06]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0001419	PMID:12200364	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-26]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0003010	OMIM:314050	IEA					P	HPO:iea[2009-02-17]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0001878	OMIM:314050	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0011877	PMID:17209061	PCS		3/3			P	HPO:probinson[2023-03-26]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0000967	PMID:17209061	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-26]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0000978	PMID:17209061	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-26]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0001923	OMIM:314050	IEA					P	HPO:iea[2009-02-17]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0033536	PMID:17209061	PCS		3/3			P	HPO:probinson[2023-03-26]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0000421	PMID:17209061	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-26]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0001873	PMID:17209061	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-26]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0001744	OMIM:314050	IEA					P	HPO:iea[2009-02-17]
OMIM:314050	Thrombocytopenia with beta-thalassemia, X-linked		HP:0031965	PMID:17209061	PCS		3/3			P	HPO:probinson[2023-03-26]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0003456	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000684	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0001156	PMID:2109828	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-30]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0004322	PMID:2109828	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0002684	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0001250	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0003472	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0003593	PMID:2109828	PCS		1/1			C	HPO:probinson[2022-05-30]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0010049	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0010743	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000939	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0009381	OMIM:103580	TAS					P	HPO:probinson[2012-06-10]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0034282	PMID:2109828	PCS		2/2			P	HPO:probinson[2022-06-04]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0100543	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000518	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000639	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0006297	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000135	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000311	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0001249	OMIM:103580	IEA					P	HPO:skoehler[2012-10-11]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000852	PMID:2109828	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0002135	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0003165	PMID:2109828	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000293	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000470	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0005280	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0002905	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000821	PMID:2109828	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0006960	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0000006	PMID:2109828	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0001513	OMIM:103580	IEA					P	HPO:iea[2009-02-17]
OMIM:103580	Pseudohypoparathyroidism, type IA		HP:0001831	OMIM:103580	TAS					P	HPO:probinson[2012-06-10]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0002850	PMID:28782633	PCS		7/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0410302	PMID:28782633	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0005215	PMID:28782633	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0003621	PMID:28782633	PCS		2/10			C	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0410299	PMID:28782633	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0002783	PMID:28782633	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0410297	PMID:28782633	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0410295	PMID:28782633	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0003593	PMID:28782633	PCS		4/10			C	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0030880	PMID:28782633	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0011108	PMID:28782633	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0001903	PMID:28782633	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0011463	PMID:28782633	PCS		4/10			C	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0011110	PMID:28782633	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0100806	PMID:28782633	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0002837	PMID:28782633	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0000403	PMID:28782633	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0000006	PMID:28782633	PCS					I	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0002720	PMID:28782633	PCS		8/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0003259	PMID:28782633	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620670	Immunodeficiency, common variable, 15		HP:0004315	PMID:28782633	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001332	OMIM:252011	IEA					P	HPO:skoehler[2010-06-18]
OMIM:252011	Mitochondrial complex II deficiency		HP:0004322	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001371	OMIM:252011	TAS					P	HPO:skoehler[2013-06-05]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001250	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001251	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0003593	PMID:10746566	PCS		1/1			C	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0000580	OMIM:252011	TAS					P	HPO:skoehler[2015-11-15]
OMIM:252011	Mitochondrial complex II deficiency		HP:0032653	PMID:10746566	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0100543	OMIM:252011	TAS					P	HPO:skoehler[2014-04-04]
OMIM:252011	Mitochondrial complex II deficiency		HP:0000639	OMIM:252011	TAS					P	HPO:skoehler[2015-08-05]
OMIM:252011	Mitochondrial complex II deficiency		HP:0008314	PMID:7550341;PMID:10746566	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-11];HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0008316	OMIM:252011	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001324	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001644	OMIM:252011	TAS					P	HPO:skoehler[2013-06-05]
OMIM:252011	Mitochondrial complex II deficiency		HP:0003546	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001347	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0004897	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0003200	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0002078	PMID:10746566	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0003487	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0002376	PMID:10746566	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0002352	OMIM:252011	TAS					P	HPO:probinson[2012-07-15]
OMIM:252011	Mitochondrial complex II deficiency		HP:0002151	PMID:10746566	PCS		1/1		HP:0012825	P	HPO:probinson[2012-04-28];HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001263	PMID:10746566	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0030682	OMIM:252011	TAS					P	HPO:skoehler[2015-12-30]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001639	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0012240	OMIM:252011	TAS					P	HPO:probinson[2013-04-01]
OMIM:252011	Mitochondrial complex II deficiency		HP:0000508	OMIM:252011	TAS					P	HPO:skoehler[2015-11-15]
OMIM:252011	Mitochondrial complex II deficiency		HP:0000602	OMIM:252011	TAS					P	HPO:skoehler[2015-11-15]
OMIM:252011	Mitochondrial complex II deficiency		HP:0006980	OMIM:252011	TAS					P	HPO:skoehler[2012-10-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0000007	PMID:7550341	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-11]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001319	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0000648	OMIM:252011	TAS					P	HPO:skoehler[2015-11-15]
OMIM:252011	Mitochondrial complex II deficiency		HP:0000505	OMIM:252011	TAS					P	HPO:skoehler[2015-08-05]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001257	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:252011	Mitochondrial complex II deficiency		HP:0001336	OMIM:252011	IEA					P	HPO:iea[2009-02-17]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000483	PMID:33537682	PCS		2/4			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001374	PMID:33537682	PCS		2/4			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001476	PMID:33537682	PCS		2/3			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000684	PMID:33537682	PCS		2/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001272	PMID:33537682	PCS		1/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001250	PMID:33537682	PCS		3/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001252	PMID:33537682	PCS		6/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0003593	PMID:33537682	PCS		3/6			C	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0033725	PMID:33537682	PCS		1/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0012469	PMID:33537682	PCS		1/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0011463	PMID:33537682	PCS		1/6			C	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000316	PMID:33537682	PCS		4/5			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000637	PMID:33537682	PCS		5/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002119	PMID:33537682	PCS		2/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001643	PMID:33537682	PCS		1/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000179	PMID:33537682	PCS		5/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002236	PMID:33537682	PCS		3/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0003623	PMID:33537682	PCS		2/6			C	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002059	PMID:33537682	PCS		1/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001187	PMID:33537682	PCS		3/4			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001344	PMID:33537682	PCS		3/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000750	PMID:33537682	PCS		6/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002650	PMID:33537682	PCS		3/5			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0031936	PMID:33537682	PCS		5/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0011968	PMID:33537682	PCS		5/5			P	HPO:probinson[2022-05-09];HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0001263	PMID:33537682	PCS		6/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002808	PMID:33537682	PCS		2/5			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002827	PMID:33537682	PCS		2/4			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000646	PMID:33537682	PCS		1/4			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002307	PMID:33537682	PCS		6/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000768	PMID:33537682	PCS		1/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000400	PMID:33537682	PCS		3/5			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000006	PMID:33537682	PCS					I	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000028	PMID:33537682	PCS		1/4			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0002104	PMID:33537682	PCS		2/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000126	PMID:33537682	PCS		1/6			P	HPO:probinson[2022-05-09]
OMIM:619797	Neurodevelopmental disorder with central hypotonia and dysmorphic facies		HP:0000687	PMID:33537682	PCS		4/5			P	HPO:probinson[2022-05-09]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001561	PMID:23933735	PCS		0/8			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0011968	PMID:23933735	PCS		5/7			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001252	PMID:23933735	PCS		8/8		HP:0012828	P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001284	PMID:23933735	PCS		8/8			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001270	PMID:23933735	PCS		5/5			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0011922	PMID:23933735	PCS		0/1			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0003391	PMID:23933735	PCS		5/5			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0030319	PMID:23933735	PCS		4/5			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0040081	PMID:23933735	PCS		0/8			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0000007	PMID:23933735	PCS					I	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0005949	PMID:23933735	PCS		3/7			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001558	PMID:23933735	PCS		0/8			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0002515	PMID:23933735	PCS		5/5			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001643	PMID:23933735	PCS		1/8			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0002910	PMID:23933735	PCS		0/8			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001631	PMID:23933735	PCS		1/8			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001623	PMID:23933735	PCS		3/7			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0002643	PMID:23933735	PCS	HP:0003623	1/7			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001612	PMID:23933735	PCS		7/7			P	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0003623	PMID:23933735	PCS		8/8			C	HPO:probinson[2022-08-22]
OMIM:619967	Myopathy, congenital, nonprogressive		HP:0001655	PMID:23933735	PCS		1/8			P	HPO:probinson[2022-08-22]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0001265	PMID:23434117	PCS					P	HPO:skoehler[2013-05-21];HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0003621	PMID:23434117	PCS		4/7			C	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0003376	PMID:23434117	PCS		4/7			P	HPO:skoehler[2013-05-21];HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0003596	PMID:23434117	PCS		1/7			C	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0001761	OMIM:615185	TAS					P	HPO:skoehler[2013-05-21]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0008959	PMID:23434117	PCS		1/7			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0002495	PMID:23434117	PCS		5/7			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0003383	PMID:23434117	PCS		2/2			P	HPO:skoehler[2013-05-21];HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0003450	OMIM:615185	TAS					P	HPO:skoehler[2013-05-21]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0011096	PMID:23434117	PCS		2/2			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0009053	PMID:23434117	PCS		7/7			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0011462	PMID:23434117	PCS		2/7			C	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0002936	OMIM:615185	TAS					P	HPO:skoehler[2013-05-21]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0007149	PMID:23434117	PCS		2/7			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0003438	PMID:23434117	PCS		6/7			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0000006	PMID:23434117	PCS					I	HPO:skoehler[2013-05-21];HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0003677	PMID:23434117	PCS					C	HPO:skoehler[2013-05-21];HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0001765	PMID:23434117	PCS		1/1			P	HPO:skoehler[2013-05-21];HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0008944	PMID:23434117	PCS		7/7			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0007328	PMID:23434117	PCS		5/7			P	HPO:probinson[2023-03-29]
OMIM:615185	Charcot-Marie-Tooth disease, dominant intermediate F		HP:0006844	PMID:23434117	PCS		6/7			P	HPO:probinson[2023-03-29]
OMIM:226960	Lowry-Wood syndrome		HP:0000340	PMID:29265708	PCS		3/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0000662	PMID:29265708	PCS		1/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0001377	PMID:30368667	PCS		1/2			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0004322	PMID:29265708	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0001156	PMID:29265708;PMID:30368667	PCS		3/5			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0003177	PMID:1183069	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0000580	PMID:29265708	PCS		1/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0010585	PMID:30368667	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0000639	PMID:1183069	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0012095	PMID:30368667	PCS		1/2			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0012471	PMID:29265708	PCS		3/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0002654	PMID:29265708	PCS		3/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0000252	PMID:29265708;PMID:30368667	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0001263	PMID:30368667	PCS		1/2			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0003182	PMID:29265708	PCS					P	HPO:probinson[2012-07-28];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0002091	PMID:29265708	PCS		1/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0001518	PMID:29265708	PCS	HP:0003577	3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0010582	PMID:1183069	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0002827	PMID:29265708	PCS		2/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0000448	PMID:29265708	PCS		3/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0000007	PMID:29265708	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0007994	PMID:29265708	PCS		1/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0004209	PMID:29265708	PCS		3/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0001511	PMID:29265708	PCS	HP:0030674	3/3			P	HPO:probinson[2020-09-15]
OMIM:226960	Lowry-Wood syndrome		HP:0002987	PMID:29265708	PCS		2/3			P	HPO:probinson[2020-09-15]
OMIM:122200	Corneal dystrophy, lattice type I		HP:0000495	OMIM:122200	IEA					P	HPO:iea[2009-02-17]
OMIM:122200	Corneal dystrophy, lattice type I		HP:0000529	OMIM:122200	IEA					P	HPO:iea[2009-02-17]
OMIM:122200	Corneal dystrophy, lattice type I		HP:0000006	OMIM:122200	IEA					I	HPO:iea[2009-02-17]
OMIM:122200	Corneal dystrophy, lattice type I		HP:0001149	OMIM:122200	TAS					P	HPO:probinson[2009-02-17]
OMIM:239840	Hypertrichosis, congenital anterior cervical, with peripheral sensory		HP:0007178	OMIM:239840	PCS					P	HPO:probinson[2012-03-12]
OMIM:239840	Hypertrichosis, congenital anterior cervical, with peripheral sensory		HP:0000007	OMIM:239840	IEA					I	HPO:iea[2009-02-17]
OMIM:239840	Hypertrichosis, congenital anterior cervical, with peripheral sensory		HP:0000763	OMIM:239840	PCS					P	HPO:probinson[2012-03-12]
OMIM:239840	Hypertrichosis, congenital anterior cervical, with peripheral sensory		HP:0002754	OMIM:239840	IEA					P	HPO:iea[2009-02-17]
OMIM:239840	Hypertrichosis, congenital anterior cervical, with peripheral sensory		HP:0004535	OMIM:239840	PCS					P	HPO:probinson[2012-03-12]
OMIM:311100	Optic atrophy--spastic paraplegia syndrome		HP:0000648	OMIM:311100	IEA					P	HPO:iea[2009-02-17]
OMIM:311100	Optic atrophy--spastic paraplegia syndrome		HP:0001417	OMIM:311100	IEA					I	HPO:iea[2009-02-17]
OMIM:311100	Optic atrophy--spastic paraplegia syndrome		HP:0004924	OMIM:311100	IEA					P	HPO:iea[2009-02-17]
OMIM:311100	Optic atrophy--spastic paraplegia syndrome		HP:0001258	OMIM:311100	IEA					P	HPO:iea[2009-02-17]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002960	PMID:34363755	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0001894	PMID:34363755	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0004322	PMID:34363755	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0000100	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0001250	PMID:34363755	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0003593	PMID:34363755	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0003271	PMID:34363755	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0001270	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0012444	PMID:34363755	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0012302	PMID:34363755	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0011123	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0008873	PMID:34363755	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002716	PMID:34363755	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002119	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0001369	PMID:34363755	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002633	PMID:34363755	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002754	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0000010	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002133	PMID:34363755	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0000750	PMID:34363755	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0011968	PMID:34363755	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0200029	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0001263	PMID:34363755	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0034786	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0011108	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0011110	PMID:34363755	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0000509	PMID:34363755	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0011473	PMID:34363755	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:4000054	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002608	PMID:34363755	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0001954	PMID:34363755	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0000007	PMID:34363755	PCS					I	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0001935	PMID:34363755	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0025722	PMID:34363755	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002027	PMID:34363755	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620880	Autoinflammation with arthritis and vasculitis		HP:0002721	PMID:34363755	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:126700	Basal laminar drusen		HP:0003596	PMID:18252232	PCS		18/24			C	HPO:probinson[2023-02-25]
OMIM:126700	Basal laminar drusen		HP:0000529	PMID:18252232	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:126700	Basal laminar drusen		HP:0003584	PMID:18252232	PCS		5/24			C	HPO:probinson[2023-02-25]
OMIM:126700	Basal laminar drusen		HP:0011510	PMID:18252232	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:126700	Basal laminar drusen		HP:0025710	PMID:18252232	PCS		1/24			C	HPO:probinson[2023-02-25]
OMIM:126700	Basal laminar drusen		HP:0000006	PMID:18252232	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0003774	PMID:12675840;PMID:10534505;PMID:11849445	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0003596	PMID:10534505	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0010637	PMID:12360495	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0000083	PMID:12675840;PMID:10534505;PMID:11849445	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0001097	PMID:11849445	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0000093	PMID:12675840;PMID:12360495	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0011034	PMID:12360495	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0001903	PMID:10534505	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0001917	PMID:12675840;PMID:10534505	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0011462	PMID:12675840	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0000822	PMID:12675840;PMID:10534505	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0009830	PMID:12360495	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0001635	PMID:10534505;PMID:12360495;PMID:11849445	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0000967	PMID:12675840	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0012280	PMID:10534505;PMID:11849445	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620658	Amyloidosis, hereditary systemic 5		HP:0000006	PMID:10534505	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:601682	Glaucoma 1, primary open angle, C		HP:0007906	OMIM:601682	IEA					P	HPO:iea[2009-02-17]
OMIM:601682	Glaucoma 1, primary open angle, C		HP:0000006	OMIM:601682	IEA					I	HPO:iea[2009-02-17]
OMIM:601682	Glaucoma 1, primary open angle, C		HP:0000501	OMIM:601682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:215400	Chordoma, susceptibility to		HP:0003621	PMID:19801981	PCS		3/16			C	HPO:probinson[2022-07-01]
OMIM:215400	Chordoma, susceptibility to		HP:0003596	PMID:19801981	PCS		4/16			C	HPO:probinson[2022-07-01]
OMIM:215400	Chordoma, susceptibility to		HP:0009592	PMID:19801981	PCS		1/16			P	HPO:probinson[2022-07-01]
OMIM:215400	Chordoma, susceptibility to		HP:0003584	PMID:19801981	PCS		1/16			C	HPO:probinson[2022-07-01]
OMIM:215400	Chordoma, susceptibility to		HP:0011462	PMID:19801981	PCS		8/16			C	HPO:probinson[2022-07-01]
OMIM:215400	Chordoma, susceptibility to		HP:0010762	PMID:19801981	PCS		15/16			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-07-01]
OMIM:215400	Chordoma, susceptibility to		HP:0000006	PMID:19801981	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0003621	PMID:35840178	PCS		1/2			C	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0001685	PMID:35840178;PMID:38436102	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0002094	PMID:38436102	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0012665	PMID:38436102	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0012666	PMID:35840178;PMID:38436102	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0012663	PMID:38436102	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0031185	PMID:35840178	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0011462	PMID:35840178;PMID:38436102	PCS		3/4			C	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0006682	PMID:38436102	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0001635	PMID:35840178	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0000007	PMID:35840178	PCS					I	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0001962	PMID:38436102	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0004756	PMID:35840178;PMID:38436102	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:620894	Cardiomyopathy, dilated, 2K		HP:0001644	PMID:35840178;PMID:38436102	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-02-17]
OMIM:262850	Plasmin inhibitor deficiency		HP:0012151	OMIM:262850	TAS					P	HPO:probinson[2012-09-16]
OMIM:262850	Plasmin inhibitor deficiency		HP:0000007	OMIM:262850	TAS					I	HPO:probinson[2009-02-17]
OMIM:262850	Plasmin inhibitor deficiency		HP:0000978	OMIM:262850	TAS					P	HPO:probinson[2009-02-17]
OMIM:262850	Plasmin inhibitor deficiency		HP:0005261	OMIM:262850	TAS					P	HPO:probinson[2009-02-17]
OMIM:262850	Plasmin inhibitor deficiency		HP:0001934	OMIM:262850	TAS					P	HPO:probinson[2009-02-17]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0003621	PMID:19590045	PCS		3/5			C	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0003596	PMID:19590045	PCS		1/5			C	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0011462	PMID:19590045	PCS		1/5			C	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0001635	PMID:19590045	PCS		4/4			P	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0033764	PMID:19590045	PCS		1/5			C	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0033755	PMID:19590045	PCS		5/5			P	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0000006	PMID:19590045	PCS					I	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0012666	PMID:19590045	PCS		4/5			P	HPO:probinson[2022-07-04]
OMIM:613286	Cardiomyopathy, dilated, 1FF		HP:0001644	PMID:19590045	PCS		2/2			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-07-04]
OMIM:612198	Diastasis recti and weakness of the linea alba		HP:0001540	OMIM:612198	TAS					P	HPO:probinson[2009-02-17]
OMIM:612198	Diastasis recti and weakness of the linea alba		HP:0009023	OMIM:612198	TAS					P	HPO:probinson[2012-07-16]
OMIM:612198	Diastasis recti and weakness of the linea alba		HP:0002019	OMIM:612198	TAS					P	HPO:probinson[2009-02-17]
OMIM:612198	Diastasis recti and weakness of the linea alba		HP:0000006	OMIM:612198	TAS					I	HPO:probinson[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001397	PMID:4022672	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001254	PMID:4022672	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0002069	PMID:4022672	PCS		1/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0003236	OMIM:201475	TAS					P	HPO:skoehler[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0003552	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0003234	PMID:4022672	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001252	PMID:4022672	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0002240	PMID:4022672	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0002020	PMID:4022672	PCS		1/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0003593	PMID:4022672	PCS		1/3			C	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0012664	PMID:4022672	PCS		1/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0009045	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001405	PMID:4022672	PCS		1/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001404	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001987	PMID:4022672	PCS		3/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001324	OMIM:201475	TAS					P	HPO:probinson[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001522	PMID:4022672	PCS		1/3			C	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001645	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0003623	PMID:4022672	PCS		2/3			C	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0005943	PMID:4022672	PCS		2/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0000252	PMID:4022672	PCS		2/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001640	PMID:4022672	PCS		2/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0002572	PMID:4022672	PCS		3/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:6000860	OMIM:201475	TAS					P	HPO:probinson[2024-08-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0033165	PMID:4022672	PCS		1/3			P	HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001639	PMID:4022672	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0001958	PMID:4022672	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0003738	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0000007	PMID:7668252	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0008305	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0002789	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:201475	Very long-chain acyl-CoA dehydrogenase deficiency		HP:0003215	OMIM:201475	IEA					P	HPO:iea[2009-02-17]
OMIM:258500	Optic atrophy 6		HP:0000639	PMID:14508503	PCS		0/4			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0011463	PMID:14508503	PCS		4/4			C	HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0000613	PMID:14508503	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0000007	PMID:14508503	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0000546	PMID:14508503	PCS		0/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0000505	PMID:14508503	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0000648	PMID:14508503	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0000642	PMID:14508503	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-09]
OMIM:258500	Optic atrophy 6		HP:0003677	PMID:14508503	PCS					C	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-09]
OMIM:615191	Lissencephaly 5		HP:0003676	OMIM:615191	TAS					C	HPO:skoehler[2017-07-13]
OMIM:615191	Lissencephaly 5		HP:0000365	OMIM:615191	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615191	Lissencephaly 5		HP:0002365	PMID:23472759	PCS		4/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0001250	PMID:23472759	PCS		4/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0002085	PMID:23472759	PCS		3/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0001252	PMID:23472759	PCS		3/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0002282	PMID:23472759	TAS					P	HPO:probinson[2015-02-22]
OMIM:615191	Lissencephaly 5		HP:0001270	PMID:23472759	PCS		4/4			P	HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0007260	PMID:23472759	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0100307	PMID:23472759	PCS		4/4			P	HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0000518	OMIM:615191	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615191	Lissencephaly 5		HP:0000238	PMID:23472759	PCS		4/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0000256	OMIM:615191	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615191	Lissencephaly 5		HP:0001249	PMID:23472759	PCS		4/4		HP:0003676	P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0001320	PMID:23472759	PCS		4/4			P	HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0032409	OMIM:615191	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615191	Lissencephaly 5		HP:0002079	PMID:23472759	PCS		3/4			P	HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0002132	OMIM:615191	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615191	Lissencephaly 5		HP:0002352	OMIM:615191	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615191	Lissencephaly 5		HP:0001263	OMIM:615191	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615191	Lissencephaly 5		HP:0011344	OMIM:615191	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615191	Lissencephaly 5		HP:0000007	PMID:23472759	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0000648	PMID:23472759	PCS		2/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-02-23]
OMIM:615191	Lissencephaly 5		HP:0001258	OMIM:615191	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615191	Lissencephaly 5		HP:0002500	PMID:23472759	PCS		4/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-02-23]
OMIM:606660	Uveal melanoma, susceptibility to, 1		HP:0007716	PMID:32239153	PCS					P	HPO:probinson[2022-08-28]
OMIM:606660	Uveal melanoma, susceptibility to, 1		HP:0003581	PMID:32239153	PCS					C	HPO:probinson[2022-08-28]
OMIM:606660	Uveal melanoma, susceptibility to, 1		HP:0000006	PMID:32239153	PCS					I	HPO:probinson[2022-08-28]
OMIM:608895	Macular degeneration, age-related, 3		HP:0003477	PMID:21576112	PCS		18/18			P	HPO:skoehler[2015-12-30]
OMIM:608895	Macular degeneration, age-related, 3		HP:0011808	PMID:21576112	PCS		18/23			P	HPO:probinson[2017-07-02]
OMIM:608895	Macular degeneration, age-related, 3		HP:0003596	PMID:21576112	PCS		4/18			C	HPO:probinson[2022-05-14]
OMIM:608895	Macular degeneration, age-related, 3		HP:0011506	PMID:21576112	PCS					P	HPO:probinson[2013-03-12]
OMIM:608895	Macular degeneration, age-related, 3		HP:0001761	PMID:21576112	PCS					P	HPO:probinson[2017-07-02]
OMIM:608895	Macular degeneration, age-related, 3		HP:0001382	PMID:21576112	PCS		2/18			P	HPO:skoehler[2015-12-30]
OMIM:608895	Macular degeneration, age-related, 3		HP:0003693	PMID:21576112	PCS		18/22			P	HPO:probinson[2017-07-02]
OMIM:608895	Macular degeneration, age-related, 3		HP:0003584	PMID:21576112	PCS		7/18			C	HPO:probinson[2022-05-14]
OMIM:608895	Macular degeneration, age-related, 3		HP:0002460	PMID:21576112	PCS		18/22			P	HPO:probinson[2017-07-02]
OMIM:608895	Macular degeneration, age-related, 3		HP:0011510	PMID:15269314	PCS					P	HPO:probinson[2013-01-09]
OMIM:608895	Macular degeneration, age-related, 3		HP:0011463	PMID:21576112	IEA		2/18			C	HPO:probinson[2022-05-14]
OMIM:608895	Macular degeneration, age-related, 3		HP:0000608	PMID:15269314	PCS	HP:0003584	9/19			P	HPO:probinson[2013-03-12]
OMIM:608895	Macular degeneration, age-related, 3		HP:0011462	PMID:21576112	PCS		5/18			C	HPO:probinson[2022-05-14]
OMIM:608895	Macular degeneration, age-related, 3		HP:0002936	PMID:21576112	PCS		HP:0040281			P	HPO:skoehler[2015-12-30]
OMIM:608895	Macular degeneration, age-related, 3		HP:0000762	OMIM:608895	TAS		HP:0040283			P	HPO:probinson[2017-08-09]
OMIM:608895	Macular degeneration, age-related, 3		HP:0000974	PMID:21576112	PCS		4/18			P	HPO:skoehler[2015-12-30]
OMIM:608895	Macular degeneration, age-related, 3		HP:0000006	OMIM:608895	TAS					I	HPO:skoehler[2017-08-09]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0001010	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0000007	OMIM:257800	IEA					I	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0001305	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0002218	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0001257	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0001510	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0002305	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0001249	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:257800	Oculocerebral syndrome with hypopigmentation		HP:0000478	OMIM:257800	IEA					P	HPO:iea[2009-02-17]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0003577	PMID:32707086	PCS		2/12			C	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0003676	PMID:32707086	PCS		11/12			C	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0003431	PMID:32707086	PCS		1/8			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0001531	PMID:32707086	PCS		3/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000343	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000463	PMID:32707086	PCS		2/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0001371	PMID:32707086	PCS		5/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0001250	PMID:32707086	PCS		9/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0012707	PMID:32707086	PCS		3/4			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0003593	PMID:32707086	PCS		8/12			C	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0001270	PMID:32707086	PCS		12/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000639	PMID:32707086	PCS		2/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0011463	PMID:32707086	PCS		1/12			C	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000316	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0020045	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000218	PMID:32707086	PCS		2/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0003448	PMID:32707086	PCS		3/8			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0020049	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000278	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0001249	PMID:32707086	PCS		12/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0003623	PMID:32707086	PCS		1/12			C	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000252	PMID:32707086	PCS		9/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002650	PMID:32707086	PCS		2/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002376	PMID:32707086	PCS		6/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002079	PMID:32707086	PCS		7/11			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002530	PMID:32707086	PCS		2/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002151	PMID:32707086	PCS		6/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000470	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002490	PMID:32707086	PCS		7/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000007	PMID:32707086	PCS					I	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000527	PMID:32707086	PCS		2/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000505	PMID:32707086	PCS		8/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002307	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000565	PMID:32707086	PCS		2/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0001258	PMID:32707086	PCS		12/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0001510	PMID:32707086	PCS		4/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0002500	PMID:32707086	PCS		12/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0000544	PMID:32707086	PCS		1/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0004887	PMID:32707086	PCS		5/12			P	HPO:probinson[2020-11-29]
OMIM:619026	Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities		HP:0003557	PMID:32707086	PCS		3/5			P	HPO:probinson[2020-11-29]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0000639	PMID:23364476	PCS		1/1		HP:0012825	P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0002286	PMID:23364476	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0007750	PMID:23364476	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0000613	PMID:23364476	PCS		1/1		HP:0012825	P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0000007	PMID:23364476	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0007663	PMID:23364476	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-12]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0000505	PMID:23364476	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-12]
OMIM:113750	Albinism, oculocutaneous, type VI		HP:0007513	PMID:23364476	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0025484	PMID:2510172	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0000750	PMID:2510172	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0033077	PMID:2510172	PCS		2/2			P	HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0011463	PMID:2510172	PCS		2/2			C	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0011788	OMIM:188570	TAS		2/2			P	HPO:probinson[2013-03-12];HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0007018	PMID:2510172	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0000853	PMID:2510172	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0000006	PMID:2510172	PCS					I	HPO:probinson[2013-03-12];HPO:probinson[2022-05-14]
OMIM:188570	Thyroid hormone resistance, generalized, autosomal dominant		HP:0002930	PMID:2510172	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0004325	PMID:26235985	PCS		12/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000365	PMID:26235985	PCS		3/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000486	PMID:26235985	PCS		2/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000463	PMID:26235985	PCS			FEMALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001250	PMID:26235985	PCS		6/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001252	PMID:26235985	PCS		29/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0003593	PMID:26235985	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000718	PMID:26235985	PCS		HP:0040283			P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000316	PMID:26235985	PCS			FEMALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000414	PMID:26235985	PCS			FEMALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0002119	PMID:26235985	PCS		13/37	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000752	PMID:26235985	PCS		HP:0040283			P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001423	PMID:26235985	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001249	PMID:26235985	PCS		38/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001249	PMID:26235985	IEA		5/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000252	PMID:26235985	PCS		12/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000252	PMID:26235985	PCS		2/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000175	PMID:26235985	PCS		3/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0002136	PMID:26235985	PCS		17/38			P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0002650	PMID:26235985	PCS		4/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000431	PMID:26235985	PCS			FEMALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0002079	PMID:26235985	PCS		13/37	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000276	PMID:26235985	PCS			FEMALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000193	PMID:26235985	PCS		1/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0005164	PMID:26235985	PCS		1/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0100660	PMID:26235985	PCS		HP:0040283			P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000708	PMID:26235985	PCS		1/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000826	PMID:26235985	PCS		5/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001419	PMID:26235985	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001257	PMID:26235985	PCS		17/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0001257	PMID:26235985	PCS		3/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000204	PMID:26235985	PCS		3/38	FEMALE		P	HPO:skoehler[2015-10-05];HPO:probinson[2020-09-02]
OMIM:300958	Intellectual developmental disorder, X-linked, syndrome, snijders Blok type		HP:0000248	PMID:26235985	PCS		3/5	MALE		P	HPO:probinson[2020-09-02]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003323	PMID:10952871	PCS		6/6			P	HPO:probinson[2012-06-05];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003198	PMID:10952871	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003044	PMID:10952871	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-20]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003273	PMID:10952871	PCS		6/6			P	HPO:probinson[2012-06-05];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003184	PMID:10952871	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0002194	PMID:10952871	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0002093	PMID:10952871	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-20]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0000007	PMID:10952871	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0000768	PMID:10952871	PCS				HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-20]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0007126	PMID:10952871	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003803	PMID:10952871	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0020203	PMID:10952871	PCS		4/4			P	HPO:probinson[2020-10-20]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0001249	PMID:10952871	PCS		0/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003798	PMID:10952871	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0001337	PMID:10952871	PCS	HP:0003623	6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-20];HPO:probinson[2024-03-10]
OMIM:605355	Nemaline myopathy 5, Amish type		HP:0003623	PMID:10952871	PCS		6/6			C	HPO:probinson[2020-10-20]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001250	PMID:28886345	PCS		3/7			P	HPO:probinson[2018-05-23];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001252	PMID:28886345	PCS		4/7			P	HPO:probinson[2018-05-23];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0003593	PMID:28886345	PCS		1/7			C	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0011463	PMID:28886345	PCS		1/7			C	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0011461	PMID:28886345	PCS		3/7			C	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001647	PMID:28886345	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000637	PMID:28886345	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001643	PMID:28886345	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000752	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001249	PMID:28886345	PCS		7/7			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0003623	PMID:28886345	PCS		2/7			C	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002553	PMID:28886345	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000252	PMID:28886345	PCS		4/7			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001344	PMID:28886345	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002079	PMID:28886345	PCS		4/6			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001382	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002198	PMID:28886345	PCS		1/6			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002195	PMID:28886345	PCS		1/6			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000407	PMID:28886345	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0007033	PMID:28886345	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000729	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001537	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000964	PMID:28886345	PCS		2/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000403	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000047	PMID:28886345	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000006	PMID:28886345	PCS					I	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000369	PMID:28886345	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002786	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000463	PMID:28886345	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002365	PMID:28886345	PCS		2/6			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002280	PMID:28886345	PCS		6/12			P	HPO:probinson[2018-05-23];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0010942	PMID:28886345	PCS	HP:0011461	1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001629	PMID:28886345	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0008872	PMID:28886345	PCS		3/6			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000733	PMID:28886345	PCS		2/7			P	HPO:probinson[2018-05-23];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0009765	PMID:28886345	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0006532	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000256	PMID:28886345	PCS		2/7			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001320	PMID:28886345	PCS		1/6			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0006956	PMID:28886345	PCS		2/6			P	HPO:probinson[2018-05-23]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002650	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001321	PMID:28886345	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000194	PMID:28886345	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000426	PMID:28886345	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001357	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0000664	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0001511	PMID:28886345	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:617751	Intellectual developmental disorder, autosomal dominant 48		HP:0002126	PMID:28886345	PCS		1/6			P	HPO:probinson[2018-05-23];HPO:probinson[2022-06-12]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0030138	PMID:30213874	PCS		2/2			P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0011870	PMID:30213874	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0011871	PMID:30213874	PCS		0/2			P	HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0011463	PMID:30213874	PCS		1/1			C	HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0008320	PMID:30213874	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0001933	PMID:30213874	TAS		2/2			P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0000007	PMID:30213874	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0011889	PMID:30213874	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0002239	PMID:30213874	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0001873	PMID:30213874	PCS		1/2		HP:0012825	P	HPO:probinson[2024-03-15]
OMIM:618462	Bleeding disorder, platelet-type, 22		HP:0004866	PMID:30213874	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0005458	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001276	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0003015	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0004325	OMIM:610758	IEA					P	HPO:skoehler[2013-01-09]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0003577	PMID:17273966	PCS		1/1			C	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0005830	OMIM:610758	IEA					P	HPO:skoehler[2013-01-09]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001531	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0004322	OMIM:610758	IEA					P	HPO:skoehler[2013-01-09]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0100490	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000581	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0003593	PMID:23623389	PCS		1/1			C	HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000639	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001627	PMID:17273966	PCS		0/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001348	PMID:23623389	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000479	PMID:17273966	PCS		0/1			P	HPO:skoehler[2015-07-19];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000358	PMID:17273966	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001347	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0002751	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000252	PMID:23623389;PMID:17273966	PCS		2/2			P	HPO:probinson[2022-04-05];HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0002353	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001321	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000078	PMID:17273966	PCS		0/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0003100	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000490	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001263	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0010455	PMID:23623389	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0003083	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001181	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0006380	PMID:23623389	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001838	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0003819	PMID:17273966	PCS		1/1			C	HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000925	PMID:17273966	PCS		0/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0002827	PMID:17273966	PCS	HP:0003577	1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000426	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001239	PMID:23623389	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000007	PMID:17273966	PCS					I	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0002804	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0001511	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0007633	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000322	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0002987	PMID:23623389	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0002126	PMID:23623389	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000347	PMID:23623389;PMID:17273966	PCS		2/2			P	HPO:probinson[2022-04-05];HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0000369	PMID:17273966	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:610758	Cerebrooculofacioskeletal syndrome 4		HP:0009879	PMID:17273966	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-04-05]
OMIM:109720	Biliary cirrhosis, primary		HP:0002613	OMIM:109720	TAS					P	HPO:skoehler[2009-02-17]
OMIM:109720	Biliary cirrhosis, primary		HP:0000006	OMIM:109720	TAS					I	HPO:skoehler[2009-02-17]
OMIM:116600	Cataract, posterior polar, 1 ctpa cataract, congenital total, included		HP:0000519	PMID:19306328	PCS					P	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:116600	Cataract, posterior polar, 1 ctpa cataract, congenital total, included		HP:0001115	PMID:19005574	PCS		12/12			P	HPO:iea[2009-02-17]
OMIM:116600	Cataract, posterior polar, 1 ctpa cataract, congenital total, included		HP:0000006	PMID:19005574	PCS					I	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:116600	Cataract, posterior polar, 1 ctpa cataract, congenital total, included		HP:0000545	OMIM:116600	PCS					P	HPO:iea[2009-02-17]
OMIM:116600	Cataract, posterior polar, 1 ctpa cataract, congenital total, included		HP:0001139	OMIM:116600	PCS					P	HPO:iea[2009-02-17]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0045081	PMID:15784703	PCS		0/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0030795	PMID:15784703	PCS		1/4			P	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0003593	PMID:15784703	PCS		1/4			C	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0003074	PMID:15784703	PCS		1/4			P	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0000819	PMID:15784703	PCS		1/4			P	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0025709	PMID:15784703	PCS		1/4			C	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0011463	PMID:15784703	PCS		1/4			C	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0004904	PMID:15784703	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0025710	PMID:15784703	PCS		1/4			C	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0040217	PMID:15784703	PCS		3/4			P	HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0009800	PMID:15784703	PCS		1/4			H	HPO:skoehler[2015-04-26];HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0000006	PMID:15784703	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-04]
OMIM:616329	Maturity-onset diabetes of the young, type 13		HP:0025329	PMID:15784703	PCS		1/4			P	HPO:probinson[2023-04-04]
OMIM:192500	Long QT syndrome 1		HP:0001663	PMID:30008122	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-06]
OMIM:192500	Long QT syndrome 1		HP:0000364	PMID:26344792	PCS		0/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06];HPO:probinson[2024-03-08]
OMIM:192500	Long QT syndrome 1		HP:0011463	PMID:30008122	PCS		1/1			C	HPO:probinson[2022-07-09]
OMIM:192500	Long QT syndrome 1		HP:0001657	PMID:8528244	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-06]
OMIM:192500	Long QT syndrome 1		HP:0005184	PMID:30008122;PMID:26344792	PCS		5/9			P	HPO:probinson[2021-09-06]
OMIM:192500	Long QT syndrome 1		HP:0001279	PMID:30008122;PMID:26344792	PCS		6/9		HP:0025377;HP:0025377	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-06];HPO:probinson[2021-09-06]
OMIM:192500	Long QT syndrome 1		HP:0001664	PMID:26344792	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-06]
OMIM:192500	Long QT syndrome 1		HP:0000006	PMID:8528244	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-06]
OMIM:192500	Long QT syndrome 1		HP:0001645	PMID:26344792	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-06]
OMIM:186575	Synovial chondromatosis, familial, with dwarfism		HP:0003510	PMID:1733839	PCS					P	HPO:iea[2009-02-17]
OMIM:186575	Synovial chondromatosis, familial, with dwarfism		HP:0002829	OMIM:186575	TAS					P	HPO:skoehler[2009-02-17]
OMIM:186575	Synovial chondromatosis, familial, with dwarfism		HP:0000006	OMIM:186575	IEA					I	HPO:iea[2009-02-17]
OMIM:180104	Retinitis pigmentosa 9		HP:0001133	OMIM:180104	TAS					P	HPO:probinson[2009-02-17]
OMIM:180104	Retinitis pigmentosa 9		HP:0007737	OMIM:180104	TAS					P	HPO:probinson[2009-02-17]
OMIM:180104	Retinitis pigmentosa 9		HP:0000662	OMIM:180104	TAS					P	HPO:probinson[2009-02-17]
OMIM:180104	Retinitis pigmentosa 9		HP:0040049	OMIM:180104	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:180104	Retinitis pigmentosa 9		HP:0000518	OMIM:180104	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:180104	Retinitis pigmentosa 9		HP:0007401	OMIM:180104	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:180104	Retinitis pigmentosa 9		HP:0000510	OMIM:180104	TAS					P	HPO:probinson[2009-02-17]
OMIM:180104	Retinitis pigmentosa 9		HP:0007688	OMIM:180104	TAS					P	HPO:probinson[2009-02-17]
OMIM:180104	Retinitis pigmentosa 9		HP:0000006	PMID:12032732	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2022-10-01]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0001639	PMID:15998695;PMID:11815426	PCS		2/2			P	HPO:probinson[2022-07-04];HPO:skoehler[2013-01-09];HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0003584	PMID:11815426	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0011462	PMID:15998695	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0001712	PMID:11815426	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0001635	PMID:15998695	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0011712	PMID:15998695	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0033764	PMID:15998695	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0000006	PMID:11815426	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0004756	PMID:15998695	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0012666	PMID:15998695	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:613251	Cardiomyopathy, familial hypertrophic, 14		HP:0032092	PMID:11815426	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0003431	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0003376	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0001761	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0003693	OMIM:302901	IEA		HP:0040283			P	HPO:probinson[2012-03-13]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0003484	OMIM:302901	IEA					P	HPO:probinson[2012-03-13]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0003482	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0001284	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0002460	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0003593	OMIM:302801	IEA					C	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0001419	OMIM:302801	IEA					I	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0009027	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0009830	OMIM:302801	IEA					P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0002936	OMIM:302801	IEA				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:302801	Charcot-Marie-Tooth disease, X-linked recessive, 2		HP:0001249	OMIM:302901	IEA		HP:0040283			P	HPO:probinson[2012-03-13]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000561	PMID:29462647	PCS		1/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002223	PMID:29462647	PCS		1/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000286	PMID:29462647	PCS		3/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001374	PMID:20113479	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000684	PMID:29462647;PMID:20113479	PCS		42/42			P	HPO:probinson[2021-02-25];HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001773	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000486	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0004322	PMID:29462647;PMID:20113479	PCS		13/13			P	HPO:probinson[2021-02-25];HPO:probinson[2021-02-25];HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002860	PMID:20113479	PCS	HP:0003581				P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000482	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0003196	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0045075	PMID:29462647	PCS		2/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0010920	PMID:20113479	PCS	HP:0003621				P	HP:probinson[2018-09-02]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000518	PMID:11471165	PCS		2/41			P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001009	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000316	PMID:29462647	PCS		3/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0008577	PMID:29462647	PCS		1/2			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002216	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001249	PMID:20113479	PCS		13/41			P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002751	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0004334	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002671	PMID:20113479	PCS	HP:0003581				P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000691	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001734	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000007	PMID:10319867	PCS					I	HP:probinson[2018-07-04];HP:probinson[2018-07-14]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000568	PMID:29462647;PMID:20113479	PCS		13/13			P	HPO:probinson[2021-02-25];HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002669	PMID:11471165	PCS	HP:0011463	13/41			P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0008404	PMID:20113479	PCS		HP:0040282			P	HP:probinson[2018-07-04];HP:probinson[2018-07-14]
OMIM:268400	Rothmund-Thomson syndrome		HP:0009778	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000685	PMID:29462647	PCS		2/2			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0006349	PMID:29462647;PMID:20113479	PCS		3/43			P	HPO:probinson[2021-02-25];HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001596	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0008070	PMID:20113479	PCS		50%			P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000939	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000218	PMID:29462647	PCS		1/1			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000653	PMID:29462647	PCS		2/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000135	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001029	PMID:11471165	PCS	HP:0003593	41/41			P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001029	PMID:29462647	PCS		3/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001545	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000396	PMID:29462647	PCS		1/2			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000395	PMID:29462647	PCS		2/2			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000992	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0004279	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001762	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0045025	PMID:29462647	PCS		3/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0011069	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0005280	PMID:29462647	PCS		3/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0001518	PMID:20113479	PCS		HP:0040282			P	HP:probinson[2018-07-04];HP:probinson[2018-07-14]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002209	PMID:29462647	PCS		3/3			P	HPO:probinson[2021-02-25]
OMIM:268400	Rothmund-Thomson syndrome		HP:0006368	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0002007	PMID:29462647;PMID:20113479	PCS		12/13			P	HPO:probinson[2021-02-25];HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0200055	PMID:29462647;PMID:20113479	PCS		12/12			P	HPO:probinson[2021-02-25];HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000028	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000501	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000303	PMID:20113479	PCS					P	HP:probinson[2018-07-04]
OMIM:268400	Rothmund-Thomson syndrome		HP:0000347	PMID:29462647	PCS		3/3			P	HPO:probinson[2021-02-25]
OMIM:200970	Ackerman syndrome		HP:0000679	OMIM:200970	IEA					P	HPO:iea[2009-02-17]
OMIM:200970	Ackerman syndrome		HP:0000007	OMIM:200970	IEA					I	HPO:iea[2009-02-17]
OMIM:200970	Ackerman syndrome		HP:0000289	OMIM:200970	TAS					P	HPO:probinson[2013-03-24]
OMIM:200970	Ackerman syndrome		HP:0000501	OMIM:200970	TAS					P	HPO:skoehler[2009-02-17]
OMIM:617023	Retinitis pigmentosa 75		HP:0003621	PMID:26720455	PCS		3/3			C	HPO:probinson[2022-10-08]
OMIM:617023	Retinitis pigmentosa 75		HP:0007737	PMID:26720455	PCS		3/3			P	HPO:probinson[2022-10-08]
OMIM:617023	Retinitis pigmentosa 75		HP:0000662	OMIM:617023	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617023	Retinitis pigmentosa 75		HP:0000980	OMIM:617023	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617023	Retinitis pigmentosa 75		HP:0031790	PMID:26720455	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-08]
OMIM:617023	Retinitis pigmentosa 75		HP:0000007	PMID:26720455	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-08]
OMIM:617023	Retinitis pigmentosa 75		HP:0007994	OMIM:617023	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617023	Retinitis pigmentosa 75		HP:0000510	PMID:26355662	PCS		3/3			P	HPO:probinson[2022-10-08]
OMIM:617023	Retinitis pigmentosa 75		HP:0007843	PMID:26720455	PCS		3/3			P	HPO:probinson[2022-10-08]
OMIM:617023	Retinitis pigmentosa 75		HP:0000545	PMID:26720455	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-08]
OMIM:618310	Diamond-Blackfan anemia 18		HP:0012133	PMID:28280134	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:618310	Diamond-Blackfan anemia 18		HP:0033074	PMID:28280134	PCS	HP:0003593	2/2			P	HPO:probinson[2020-10-13]
OMIM:618310	Diamond-Blackfan anemia 18		HP:0000006	PMID:28280134	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-13]
OMIM:618310	Diamond-Blackfan anemia 18		HP:0001875	PMID:28280134	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-10-13]
OMIM:618310	Diamond-Blackfan anemia 18		HP:0012139	PMID:28280134	PCS		2/2			P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000684	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0002164	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0008873	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0001305	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0006035	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0002857	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0006477	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000774	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000773	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000039	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0001249	OMIM:225500	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0003026	OMIM:225500	TAS					P	HPO:probinson[2012-05-08]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000695	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0001762	OMIM:225500	TAS					P	HPO:probinson[2012-06-04]
OMIM:225500	Ellis-Van creveld syndrome		HP:0001162	OMIM:225500	TAS					P	HPO:probinson[2012-06-04]
OMIM:225500	Ellis-Van creveld syndrome		HP:0001241	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0011565	OMIM:225500	TAS					P	HPO:probinson[2015-02-22]
OMIM:225500	Ellis-Van creveld syndrome		HP:0010454	OMIM:225500	TAS					P	HPO:probinson[2015-02-22]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000968	OMIM:225500	TAS					P	HPO:skoehler[2015-01-14]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000668	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000888	ISBN:3642035590	TAS					P	HPO:probinson[2015-02-28]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000007	OMIM:225500	TAS					I	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000768	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0008921	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0001830	OMIM:225500	TAS					P	HPO:probinson[2012-06-04]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000047	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0001631	OMIM:225500	TAS					P	HPO:probinson[2015-02-22]
OMIM:225500	Ellis-Van creveld syndrome		HP:0002866	OMIM:225500	TAS					P	HPO:probinson[2015-02-22]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000028	OMIM:225500	TAS					P	HPO:probinson[2009-02-17]
OMIM:225500	Ellis-Van creveld syndrome		HP:0000204	OMIM:225500	TAS					P	HPO:skoehler[2010-06-20]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0000271	OMIM:601127	IEA					P	HPO:iea[2009-02-17]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0001508	OMIM:601127	IEA					P	HPO:iea[2009-02-17]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0001629	OMIM:601127	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0001719	OMIM:601127	IEA					P	HPO:iea[2009-02-17]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0001636	OMIM:601127	IEA					P	HPO:iea[2009-02-17]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0000007	OMIM:601127	IEA					I	HPO:iea[2009-02-17]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0001642	OMIM:601127	IEA					P	HPO:iea[2009-02-17]
OMIM:601127	Fallot complex with severe mental and growth retardation		HP:0001249	OMIM:601127	IEA					P	HPO:iea[2009-02-17]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000286	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002300	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002465	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0003676	PMID:30982609	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0010804	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001250	PMID:30982609	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0003034	PMID:30982609	PCS		4/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002063	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001251	PMID:30982609	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002180	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000639	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0011463	PMID:30982609	PCS					C	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0007165	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000238	PMID:30982609	PCS	HP:0003577	2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001249	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002510	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0005464	PMID:30982609	PCS		2/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001260	PMID:30982609	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001263	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0004330	PMID:30982609	PCS		4/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0100861	PMID:30982609	PCS		2/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000926	PMID:30982609	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000007	PMID:30982609	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000527	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000648	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002901	OMIM:618476	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000768	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0007359	PMID:30982609	PCS		2/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001257	PMID:30982609	PCS		3/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0003016	PMID:30982609	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0003577	PMID:30982609	PCS					C	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001591	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001274	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002280	PMID:30982609	PCS		2/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0100543	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0011002	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000414	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001305	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002119	PMID:30982609	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002514	PMID:30982609	PCS		4/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000256	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001268	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0004975	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001347	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0003621	PMID:30982609	PCS					C	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001321	OMIM:618476	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0001288	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000748	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0002808	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0007099	PMID:30982609	PCS		1/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0030890	PMID:30982609	PCS		2/4			P	HPO:probinson[2022-11-07]
OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		HP:0000505	PMID:30982609	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:254500	Multiple myeloma		HP:0001442	OMIM:254500	TAS					I	HPO:skoehler[2012-10-17]
OMIM:254500	Multiple myeloma		HP:0011034	OMIM:254500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:254500	Multiple myeloma		HP:0003581	PMID:23502783	PCS					C	HPO:probinson[2022-06-16]
OMIM:254500	Multiple myeloma		HP:0031047	OMIM:254500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254500	Multiple myeloma		HP:0006775	OMIM:254500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002421	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000340	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0003676	PMID:29691655	PCS					C	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0003577	PMID:30275004;PMID:29691655	PCS		3/4			C	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002540	OMIM:617802	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002783	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001250	PMID:30275004;PMID:29691655;PMID:26539891	PCS		4/7			P	HPO:probinson[2022-08-14];HPO:skoehler[2018-10-08];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002120	PMID:26539891	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001272	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0003196	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002283	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001252	PMID:30275004	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002580	PMID:30275004	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0003593	PMID:29691655	PCS		1/2			C	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001290	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001270	PMID:29691655	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0500041	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0011182	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000733	PMID:30275004	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0008513	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000237	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001249	PMID:30275004	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001623	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001622	PMID:30275004	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000253	PMID:29691655	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000252	PMID:30275004;PMID:29691655;PMID:26539891	PCS		7/7			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002015	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002059	PMID:29691655	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002133	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001344	PMID:30275004	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000695	PMID:30275004	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0002079	PMID:29691655	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001263	PMID:29691655;PMID:26539891	PCS		4/5			P	HPO:probinson[2022-08-14];HPO:skoehler[2018-10-08];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0005280	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000007	PMID:26539891	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000527	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0006466	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0007359	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0001612	PMID:29691655	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000545	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000347	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:617802	Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy		HP:0000369	PMID:29691655	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0003577	PMID:33242826	PCS		3/3			C	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0002980	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0005474	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0003031	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0002240	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0003274	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0004482	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0010034	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000938	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0009487	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000879	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0006610	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000476	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000773	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0003865	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000054	PMID:33242826	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0001762	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000474	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000470	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0005280	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0006385	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000926	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000007	PMID:33242826	PCS					I	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0002804	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0003417	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0003316	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0001511	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000465	PMID:33242826	PCS		2/3			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0001631	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000883	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0002866	PMID:33242826	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0005736	PMID:33242826	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:620076	Bent bone dysplasia syndrome 2		HP:0000049	PMID:33242826	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002322	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002345	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0008209	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002067	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000365	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001310	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001272	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0031629	OMIM:300623	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002066	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000020	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001152	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002080	PMID:11445641	PCS		5/5			P	HPO:probinson[2012-04-30];HPO:probinson[2022-08-13]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000716	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000639	OMIM:300623	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0008770	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000739	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000734	OMIM:300623	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001423	PMID:11445641	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-13]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001268	PMID:11445641	PCS		5/5			P	HPO:probinson[2012-04-30];HPO:probinson[2022-08-13]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0003326	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001265	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001300	PMID:11445641	PCS		5/5			P	HPO:probinson[2012-04-30];HPO:probinson[2022-08-13]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000298	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002354	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0001260	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0003584	PMID:11445641	PCS		5/5			C	HPO:probinson[2022-08-13]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002075	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002174	OMIM:300623	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000726	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0007010	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002607	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0002506	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0009830	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000821	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0000802	PMID:11445641	PCS		5/5			P	HPO:probinson[2012-04-30];HPO:probinson[2022-08-13]
OMIM:300623	Fragile X tremor/ataxia syndrome		HP:0006886	OMIM:309550	TAS					P	HPO:probinson[2012-04-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0002069	PMID:33085104	PCS		5/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0003621	PMID:33085104	PCS		4/6			C	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0001310	PMID:33085104	PCS		3/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0001288	PMID:33085104	PCS		6/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0001260	PMID:33085104	PCS		4/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0001251	PMID:33085104	PCS		6/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0000716	PMID:33085104	PCS		2/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0011462	PMID:33085104	PCS		2/6			C	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0000739	PMID:33085104	PCS		1/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0000007	PMID:33085104	PCS					I	HPO:probinson[2021-03-30];HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0001268	PMID:33085104	PCS		3/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0007018	PMID:33085104	PCS		1/6			P	HPO:probinson[2021-03-30]
OMIM:619191	Epilepsy, progressive myoclonic, 12		HP:0001336	PMID:33085104	PCS		6/6			P	HPO:probinson[2021-03-30];HPO:probinson[2021-03-30]
OMIM:615973	Cone-Rod dystrophy 20		HP:0001133	PMID:25018096	PCS		4/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0007737	PMID:25018096	PCS		2/4			P	HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0000552	PMID:25018096	PCS		2/3			P	HPO:probinson[2022-10-18];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0003593	PMID:25018096	PCS		1/2			C	HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0011003	PMID:25018096	PCS		1/4			P	HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0000639	PMID:25018096	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0011463	PMID:25018096	PCS		1/2			C	HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0007663	PMID:25018096	PCS		4/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0000007	PMID:25018096	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0000505	PMID:25018096	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0000548	PMID:25018096	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0000603	PMID:25018096	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-18]
OMIM:615973	Cone-Rod dystrophy 20		HP:0000543	PMID:25018096	PCS		1/4			P	HPO:probinson[2022-10-18]
OMIM:620704	Encephalopathy, porphyria-related		HP:0003577	PMID:14970743	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0000343	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0002188	PMID:15534187	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0010808	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0002240	PMID:14970743;PMID:15534187;PMID:1577472	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0001251	PMID:14970743;PMID:1577472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:6000536	PMID:14970743;PMID:15534187	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0000280	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0002080	PMID:14970743;PMID:1577472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0000518	PMID:14970743;PMID:15534187;PMID:1577472	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0007141	PMID:15534187	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0001903	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0011463	PMID:1577472	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0031890	PMID:14970743;PMID:15534187;PMID:1577472	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0008897	PMID:14970743;PMID:1577472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0001744	PMID:14970743;PMID:15534187;PMID:1577472	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0040318	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0002951	PMID:14970743;PMID:1577472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0003623	PMID:15534187	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0001265	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0008936	PMID:15534187	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0003487	PMID:15534187	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0002373	PMID:14970743;PMID:1577472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0001263	PMID:14970743;PMID:15534187;PMID:1577472	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0032002	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0000609	PMID:1577472	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:4000199	PMID:14970743;PMID:15534187;PMID:1577472	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0002808	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0002904	PMID:14970743;PMID:15534187;PMID:1577472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0006286	PMID:14970743;PMID:1577472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0000508	PMID:15534187	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:620704	Encephalopathy, porphyria-related		HP:0000007	PMID:1577472	PCS					I	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0000407	OMIM:608088	IEA					P	HPO:iea[2009-02-17]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0001609	OMIM:608088	IEA					P	HPO:iea[2009-02-17]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0002020	OMIM:608088	IEA					P	HPO:iea[2009-02-17]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0002936	OMIM:608088	IEA					P	HPO:iea[2009-02-17]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0012735	OMIM:608088	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0000802	OMIM:608088	IEA					P	HPO:iea[2009-02-17]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0003390	OMIM:608088	IEA					P	HPO:iea[2009-02-17]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0001279	OMIM:608088	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0000006	OMIM:608088	IEA					I	HPO:iea[2009-02-17]
OMIM:608088	Neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux		HP:0000522	OMIM:608088	IEA					P	HPO:iea[2009-02-17]
OMIM:619185	Joubert syndrome 37		HP:0025186	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000463	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0004322	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0002240	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0003593	PMID:32453716	PCS		4/5			C	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0001290	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0008070	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0002938	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0011461	PMID:32453716	PCS		1/5			C	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000316	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000657	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0002419	PMID:32453716	PCS		4/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000218	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0006610	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0008734	PMID:32453716	PCS		2/4			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000358	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0001320	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000054	PMID:32453716	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000431	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000475	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0001344	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0002079	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0005487	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0001382	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000490	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0001263	PMID:32453716	PCS		4/4			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0100259	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000729	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000508	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000007	PMID:32453716	PCS					I	HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000568	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0002007	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000369	PMID:32453716	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000028	PMID:32453716	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0001513	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000445	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:619185	Joubert syndrome 37		HP:0000126	PMID:32453716	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0002465	PMID:27694521	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0031936	PMID:27694521	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0001250	PMID:27694521	PCS	HP:0003593	3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0003155	PMID:27694521	PCS		0/3			P	HPO:nvasilevsky[2019-03-27];HPO:probinson[2024-03-15]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0001263	PMID:27694521	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0003593	PMID:27694521	PCS		3/3			C	HPO:probinson[2024-03-15]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0000007	PMID:27694521	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:617816	Glycosylphosphatidylinositol biosynthesis defect 16		HP:0001249	PMID:27694521	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:167600	Palmaris longus muscle, absence of		HP:0000924	OMIM:167600	IEA					P	HPO:iea[2009-02-17]
OMIM:167600	Palmaris longus muscle, absence of		HP:0000006	OMIM:167600	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0000252	PMID:32576952	PCS		2/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0001156	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0000034	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0004322	PMID:32576952	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0001263	PMID:32576952	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0003593	PMID:32576952	PCS		3/3			C	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0002194	PMID:32576952	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0010862	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0001181	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0012413	PMID:32576952	PCS		1/1			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0011623	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0009890	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0011220	PMID:32576952	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0002209	PMID:32576952	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0000954	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0000007	PMID:32576952	PCS					I	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0000256	PMID:32576952	PCS		1/3			P	HPO:probinson[2022-10-02]
OMIM:620062	Developmental delay with short stature, dysmorphic facial features, and sparse hair 2		HP:0000369	PMID:32576952	PCS		3/3			P	HPO:probinson[2022-10-02]
OMIM:610189	Senior-Loken syndrome 6		HP:0003774	PMID:16682973	PCS	HP:0003621	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:610189	Senior-Loken syndrome 6		HP:0006817	PMID:16682973	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-14]
OMIM:610189	Senior-Loken syndrome 6		HP:0011463	PMID:16682973	PCS		2/2			C	HPO:probinson[2023-02-20]
OMIM:610189	Senior-Loken syndrome 6		HP:0000007	PMID:16682973	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:610189	Senior-Loken syndrome 6		HP:0007663	PMID:16682973	PCS	HP:0011463	2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-20]
OMIM:610189	Senior-Loken syndrome 6		HP:0000505	PMID:16682973	PCS	HP:0011463	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:610189	Senior-Loken syndrome 6		HP:0000510	PMID:16682973	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0003577	PMID:34115842	PCS		1/10			C	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0410253	PMID:34115842	PCS		10/10			P	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0001250	PMID:34115842	PCS		2/10			P	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0000518	PMID:34115842	PCS		2/10			P	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0011463	PMID:34115842	PCS		4/10			C	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0001263	PMID:34115842	PCS		1/10			P	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0003593	PMID:34115842	PCS		5/10			C	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0000006	PMID:34115842	PCS					I	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0001744	PMID:34115842	PCS		2/10			P	HPO:probinson[2022-06-27]
OMIM:619813	Neutropenia, severe congenital, 9, autosomal dominant		HP:0003535	PMID:34115842	PCS		0/5			P	HPO:probinson[2022-06-27]
OMIM:612946	Hadziselimovic syndrome		HP:0000286	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000486	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0002023	OMIM:612946	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612946	Hadziselimovic syndrome		HP:0000089	OMIM:612946	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612946	Hadziselimovic syndrome		HP:0000463	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0004322	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001252	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0010806	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001290	OMIM:612946	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612946	Hadziselimovic syndrome		HP:0001508	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001629	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000218	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0004935	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000179	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001620	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000358	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001249	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000252	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001344	OMIM:612946	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612946	Hadziselimovic syndrome		HP:0001321	OMIM:612946	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612946	Hadziselimovic syndrome		HP:0002750	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0002079	OMIM:612946	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612946	Hadziselimovic syndrome		HP:0001263	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000294	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000508	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000426	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001636	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000007	OMIM:612946	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000601	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001714	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0001631	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612946	Hadziselimovic syndrome		HP:0000369	OMIM:612946	IEA					P	HPO:skoehler[2010-06-19]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0000011	PMID:31708116	PCS		2/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0000076	PMID:31708116	PCS		2/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0000010	PMID:31708116	PCS		2/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0001278	PMID:31708116	PCS		1/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0001508	PMID:31708116	PCS		1/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0030211	PMID:31708116	PCS		4/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0002020	PMID:31708116	PCS		1/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0012624	PMID:31708116	PCS		2/5			P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0000007	PMID:31708116	PCS					I	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0000047	PMID:31708116	PCS		1/3	MALE		P	HPO:probinson[2020-07-26]
OMIM:191800	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT		HP:0000126	PMID:31708116	PCS		2/5			P	HPO:probinson[2020-07-26]
OMIM:613480	Lymphatic malformation 3		HP:0003621	PMID:20537300	PCS		17/28			C	HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0011463	PMID:20537300	PCS		2/28			C	HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0011462	PMID:20537300	PCS		3/28			C	HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0003829	PMID:20537300	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0100658	PMID:20537300	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0001581	PMID:20537300	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0003593	PMID:20537300	PCS		6/28			C	HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0001004	PMID:20537300	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-01-30]
OMIM:613480	Lymphatic malformation 3		HP:0000006	PMID:20537300	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:617180	Chitayat syndrome		HP:0000341	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0003577	PMID:27738187	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0000343	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0000463	PMID:27738187;PMID:30569521	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-05-28];HPO:skoehler[2017-07-13];HPO:probinson[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0001156	PMID:27738187	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0004322	PMID:27738187	PCS	HP:0011463				P	HPO:probinson[2019-05-01];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0002780	PMID:27738187;PMID:30569521	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-28];HPO:skoehler[2017-07-13];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0002000	OMIM:617180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617180	Chitayat syndrome		HP:0001252	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0004220	PMID:27738187;PMID:30569521	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0002020	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0001290	PMID:27738187	PCS		1/5			P	HPO:skoehler[2017-07-13]
OMIM:617180	Chitayat syndrome		HP:0001270	PMID:27738187;PMID:30569521	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0010107	PMID:27738187	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0012471	PMID:27738187	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617180	Chitayat syndrome		HP:0000316	PMID:27738187;PMID:30569521	PCS		5/5			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0001822	PMID:27738187	PCS		5/5			P	HPO:probinson[2019-05-01];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0002779	PMID:27738187;PMID:30569521	PCS		1/6			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0001643	PMID:27738187;PMID:30569521	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0003623	PMID:30569521	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0005469	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0000396	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0001561	PMID:27738187;PMID:30569521	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-05-28];HPO:skoehler[2017-07-13];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0000750	PMID:27738187	PCS		1/5			P	HPO:probinson[2019-05-01];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0000431	PMID:27738187;PMID:30569521	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0030367	PMID:27738187;PMID:30569521	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0002098	PMID:27738187;PMID:30569521	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-28];HPO:skoehler[2018-10-08];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0001263	PMID:30569521	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0005280	PMID:27738187;PMID:30569521	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-28];HPO:skoehler[2017-07-13];HPO:probinson[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0032965	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0034197	PMID:27738187	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0009110	PMID:27738187;PMID:30569521	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0000767	PMID:27738187;PMID:30569521	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-05-28];HPO:skoehler[2019-04-18];HPO:probinson[2019-05-01]
OMIM:617180	Chitayat syndrome		HP:0009577	PMID:27738187;PMID:30569521	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0004209	PMID:27738187;PMID:30569521	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0002205	PMID:27738187;PMID:30569521	PCS		3/6			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0000520	PMID:27738187;PMID:30569521	PCS		2/6			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0009536	PMID:27738187	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-28]
OMIM:617180	Chitayat syndrome		HP:0000006	PMID:27738187	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-05-01]
OMIM:166250	Osteoglophonic dysplasia		HP:0003510	PMID:16470795;PMID:15625620	PCS		7/7			P	HPO:probinson[2023-06-08];HPO:probinson[2023-06-08];HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0001773	OMIM:166250	TAS					P	HPO:probinson[2013-04-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000882	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000684	PMID:15625620	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0100490	PMID:15625620	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0003196	PMID:15625620	PCS		1/5			P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0003593	PMID:16470795	PCS		1/2			C	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000041	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0010049	OMIM:166250	TAS					P	HPO:probinson[2012-06-03]
OMIM:166250	Osteoglophonic dysplasia		HP:0011463	PMID:16470795	PCS		1/2			C	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000316	PMID:16470795	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0001800	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0002659	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0001769	OMIM:166250	TAS					P	HPO:probinson[2013-04-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0001169	OMIM:166250	TAS					P	HPO:probinson[2013-04-07]
OMIM:166250	Osteoglophonic dysplasia		HP:0005864	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000494	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000453	PMID:15625620	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0001783	OMIM:166250	TAS					P	HPO:probinson[2012-05-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0011800	PMID:16470795;PMID:15625620	PCS		6/7			P	HPO:probinson[2023-06-08];HPO:skoehler[2013-11-28];HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000926	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000767	PMID:15625620	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000327	PMID:15625620	PCS		3/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0009778	PMID:15625620	PCS		2/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000520	PMID:15625620	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000047	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000369	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000006	PMID:15625620	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0006009	OMIM:166250	TAS					P	HPO:probinson[2013-04-07]
OMIM:166250	Osteoglophonic dysplasia		HP:0008905	PMID:16470795;PMID:15625620	PCS		2/7			P	HPO:probinson[2023-06-08];HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000343	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000023	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0001156	PMID:15625620	PCS		2/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000463	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0001230	OMIM:166250	TAS					P	HPO:probinson[2012-06-03]
OMIM:166250	Osteoglophonic dysplasia		HP:0010743	OMIM:166250	TAS					P	HPO:probinson[2012-05-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0001508	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000938	PMID:15625620	PCS		2/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000218	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0001742	OMIM:166250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0009803	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000336	PMID:15625620	PCS		3/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0002676	OMIM:166250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:166250	Osteoglophonic dysplasia		HP:0009826	OMIM:166250	TAS					P	HPO:probinson[2012-05-27]
OMIM:166250	Osteoglophonic dysplasia		HP:0001363	PMID:16470795;PMID:15625620	PCS		7/7			P	HPO:probinson[2023-06-08];HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0004279	OMIM:166250	TAS					P	HPO:probinson[2013-04-07]
OMIM:166250	Osteoglophonic dysplasia		HP:0000750	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0002098	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000470	PMID:15625620	PCS		2/5			P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000272	PMID:15625620	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0005280	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0011304	PMID:15625620	PCS		2/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000506	PMID:15625620	PCS		3/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000706	PMID:16470795;PMID:15625620	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-08];HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0006487	OMIM:166250	TAS					P	HPO:probinson[2012-05-27]
OMIM:166250	Osteoglophonic dysplasia		HP:0002007	PMID:16470795	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000586	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0001510	PMID:15625620	PCS		4/5			P	HPO:probinson[2023-06-08]
OMIM:166250	Osteoglophonic dysplasia		HP:0000303	PMID:16470795	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:166250	Osteoglophonic dysplasia		HP:0000028	OMIM:166250	IEA					P	HPO:iea[2009-02-17]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0001561	PMID:27616481	PCS		6/6			P	HPO:skoehler[2019-09-07]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0003577	PMID:27616481	PCS		1/6			C	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0002089	PMID:27616481	PCS		5/6			P	HPO:skoehler[2017-07-13]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0001371	PMID:27616481	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0005684	PMID:27616481	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0012785	PMID:27616481	PCS		2/6			P	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0012385	PMID:27616481	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0034197	PMID:27616481	PCS		5/6			C	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0000308	PMID:27616481	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0001558	PMID:27616481	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0000007	PMID:27616481	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0001511	PMID:27616481	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0000278	PMID:27616481	PCS		1/6			P	HPO:skoehler[2017-07-13]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0002987	PMID:27616481	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:617194	Lethal congenital contracture syndrome 11		HP:0001776	PMID:27616481	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:218050	Cramps, familial adolescent		HP:0003236	OMIM:218050	IEA					P	HPO:iea[2009-02-17]
OMIM:218050	Cramps, familial adolescent		HP:0003011	OMIM:218050	IEA					P	HPO:iea[2009-02-17]
OMIM:218050	Cramps, familial adolescent		HP:0000007	OMIM:218050	IEA					I	HPO:iea[2009-02-17]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0003577	PMID:19525956	PCS		1/16			C	HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0030356	PMID:19525956	PCS		8/8			P	HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0001371	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0030674	PMID:19525956	PCS		1/16			C	HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0003593	PMID:19525956	PCS		11/16			C	HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0000958	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0000737	PMID:19525956	PCS		3/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0011463	PMID:19525956	PCS		2/16			C	HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0007321	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0008872	PMID:19525956	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0002415	PMID:19525956	PCS		17/18			P	HPO:probinson[2013-04-07];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0003623	PMID:19525956	PCS		1/16			C	HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0007229	PMID:19525956	PCS		12/19			P	HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0008936	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0002135	PMID:19525956	PCS		15/19			P	HPO:probinson[2013-04-07];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0000252	OMIM:612952	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0002352	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0200149	PMID:19525956	PCS		9/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0001263	PMID:19525956	PCS		14/14			P	HPO:probinson[2013-04-07];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0003040	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0040189	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0000007	PMID:19525956	PCS					I	HPO:probinson[2013-04-07];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0009710	PMID:19525956	PCS		8/14			P	HPO:probinson[2013-04-07];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0001257	PMID:19525956	PCS		5/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:612952	Aicardi-Goutieres syndrome 5		HP:0001873	OMIM:612952	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0002850	PMID:19666484	PCS		2/2			P	HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0410300	PMID:19666484	PCS		2/2			P	HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0005387	PMID:19666484	PCS		2/2			P	HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0003581	PMID:19666484	PCS		2/2			C	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0002718	OMIM:613494	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0011839	PMID:19666484	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0000007	PMID:19666484	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0006532	PMID:19666484	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0011108	PMID:19666484	PCS		1/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-05-09]
OMIM:613494	Immunodeficiency, common variable, 4		HP:0004315	PMID:19666484	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:251450	Desbuquois dysplasia 1		HP:0003510	OMIM:251450	TAS	HP:0003577				P	HPO:skoehler[2012-11-21]
OMIM:251450	Desbuquois dysplasia 1		HP:0006429	OMIM:251450	TAS					P	HPO:skoehler[2012-11-21]
OMIM:251450	Desbuquois dysplasia 1		HP:0000160	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0001373	OMIM:251450	TAS					P	HPO:probinson[2012-07-30]
OMIM:251450	Desbuquois dysplasia 1		HP:0001252	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0003196	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0001290	OMIM:251450	TAS					P	HPO:skoehler[2017-07-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0003071	OMIM:251450	TAS					P	HPO:skoehler[2013-04-18]
OMIM:251450	Desbuquois dysplasia 1		HP:0000319	PMID:7977470	PCS		4/7			P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0003828	OMIM:251450	TAS					M	HPO:skoehler[2012-11-21]
OMIM:251450	Desbuquois dysplasia 1		HP:0010097	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0009467	PMID:7977470	PCS		6/7			P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0002812	PMID:14679587	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0003307	PMID:14679587	PCS		4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001763	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0000311	PMID:7977470	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001249	PMID:14679587	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0002673	PMID:14679587	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001382	PMID:7977470	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0005067	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0011800	OMIM:251450	TAS					P	HPO:skoehler[2013-11-28]
OMIM:251450	Desbuquois dysplasia 1		HP:0008082	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0000926	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0000007	OMIM:251450	IEA					I	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0009774	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0009611	PMID:14679587	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001852	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0000520	OMIM:251450	TAS					P	HPO:probinson[2012-07-30]
OMIM:251450	Desbuquois dysplasia 1		HP:0003016	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0000343	PMID:7977470	PCS		4/7			P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001156	OMIM:251450	TAS					P	HPO:skoehler[2014-11-26]
OMIM:251450	Desbuquois dysplasia 1		HP:0033102	PMID:7977470	PCS					P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001270	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0010068	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0010743	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0100864	OMIM:251450	TAS					P	HPO:skoehler[2012-11-22]
OMIM:251450	Desbuquois dysplasia 1		HP:0000939	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0010034	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0011120	PMID:7977470	PCS		5/7			P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0008873	PMID:7977470	PCS	HP:0003577	7/7		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0002515	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0002758	OMIM:251450	TAS					P	HPO:skoehler[2012-11-21]
OMIM:251450	Desbuquois dysplasia 1		HP:0000774	PMID:7977470	PCS		5/7			P	HPO:probinson[2012-07-30];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0006439	OMIM:251450	TAS					P	HPO:probinson[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0002650	PMID:14679587	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001762	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0002970	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0004233	PMID:14679587	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001087	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0000272	PMID:7977470	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0000470	PMID:7977470	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0005280	OMIM:251450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0003180	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:6000868	PMID:14679586	PCS		5/25			P	HPO:probinson[2024-08-03]
OMIM:251450	Desbuquois dysplasia 1		HP:0002808	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0000308	PMID:7977470	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0006243	OMIM:251450	TAS					P	HPO:probinson[2009-02-17]
OMIM:251450	Desbuquois dysplasia 1		HP:0001511	PMID:7977470	PCS	HP:0003577	7/7			P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0001510	PMID:7977470	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0000545	OMIM:251450	TAS	HP:0003584				P	HPO:skoehler[2012-11-21]
OMIM:251450	Desbuquois dysplasia 1		HP:0001513	PMID:14679587	PCS	HP:0003581	4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0002643	PMID:7977470	PCS		3/9			P	HPO:probinson[2020-10-13]
OMIM:251450	Desbuquois dysplasia 1		HP:0008108	OMIM:251450	IEA					P	HPO:iea[2009-02-17]
OMIM:611283	Isobutyryl-CoA dehydrogenase deficiency		HP:0003234	OMIM:611283	TAS					P	HPO:probinson[2013-04-01]
OMIM:611283	Isobutyryl-CoA dehydrogenase deficiency		HP:0001903	OMIM:611283	TAS					P	HPO:probinson[2013-04-01]
OMIM:611283	Isobutyryl-CoA dehydrogenase deficiency		HP:0001252	OMIM:611283	TAS					P	HPO:probinson[2013-04-01]
OMIM:611283	Isobutyryl-CoA dehydrogenase deficiency		HP:0000007	OMIM:611283	TAS					I	HPO:probinson[2013-04-01]
OMIM:611283	Isobutyryl-CoA dehydrogenase deficiency		HP:0001644	OMIM:611283	TAS					P	HPO:probinson[2013-01-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0000364	PMID:26027498	PCS		0/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0004322	PMID:26027498	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0003396	PMID:26027498	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0003199	PMID:26027498	PCS		1/2			P	HPO:skoehler[2015-08-16]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0001252	PMID:26027498	PCS		1/2			P	HPO:skoehler[2015-08-16]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0003593	PMID:26027498	PCS		1/2			C	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0000939	PMID:26027498	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0006470	PMID:26027498	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0011463	PMID:26027498	PCS		1/2			C	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0002757	PMID:26027498	PCS		2/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0000977	PMID:26027498	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0001324	PMID:26027498	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0002953	PMID:26027498	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0003865	PMID:26027498	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0002751	PMID:26027498	PCS		2/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0000750	PMID:26027498	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0001382	PMID:26027498	PCS		2/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0002194	PMID:26027498	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0030746	PMID:26027498	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0006086	PMID:26027498	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0002827	PMID:26027498	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0000926	PMID:26027498	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0000007	PMID:26027498	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0000703	PMID:26027498	PCS		0/2			P	HPO:probinson[2023-04-09]
OMIM:616507	Osteogenesis imperfecta, type XVII		HP:0004349	PMID:26027498	PCS		2/2			P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:229500	Fructose and galactose intolerance		HP:0005973	OMIM:229500	IEA					P	HPO:iea[2009-02-17]
OMIM:229500	Fructose and galactose intolerance		HP:0001250	OMIM:229500	IEA					P	HPO:iea[2009-02-17]
OMIM:229500	Fructose and galactose intolerance		HP:0004919	OMIM:229500	TAS					P	HPO:probinson[2009-02-17]
OMIM:229500	Fructose and galactose intolerance		HP:0000007	OMIM:229500	IEA					I	HPO:iea[2009-02-17]
OMIM:229500	Fructose and galactose intolerance		HP:0001943	OMIM:229500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0003236	PMID:20096397	PCS		12/12			P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0003731	PMID:20096397	PCS		5/12			P	HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0003596	PMID:20096397	PCS		6/12			C	HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0009053	PMID:20096397	PCS		7/12			P	HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0008959	PMID:20096397	PCS		0/12			P	HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0003551	PMID:20096397	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0008981	PMID:20096397	PCS		4/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0011462	PMID:20096397	PCS		6/12			C	HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0009046	PMID:20096397	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0003560	PMID:20096397	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0000007	PMID:20096397	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2023-02-18]
OMIM:613319	Miyoshi muscular dystrophy 3		HP:0009050	PMID:20096397	PCS		7/12			P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-18]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0003676	OMIM:615768	TAS					C	HPO:skoehler[2015-12-30]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0002078	PMID:24312598	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0001321	OMIM:615768	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0003487	PMID:24312598	PCS		3/6			P	HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0001272	PMID:24312598	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0001260	PMID:24312598	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0002070	PMID:24312598	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0011448	OMIM:615768	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0100543	PMID:24312598	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0000639	PMID:24312598	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0000007	PMID:24312598	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0002317	OMIM:615768	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0000135	OMIM:615768	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0001257	OMIM:615768	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0001337	OMIM:615768	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0000544	PMID:24312598	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-06-25]
OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16		HP:0001347	PMID:24312598	PCS		4/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-06-25]
OMIM:260100	Pa polymorphism of alpha-2-globulin		HP:0000007	OMIM:260100	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:260100	Pa polymorphism of alpha-2-globulin		HP:0010701	OMIM:260100	IEA					P	HPO:skoehler[2009-02-17]
OMIM:606072	Rippling muscle disease		HP:0003236	PMID:9537420	PCS		8/8			P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-19];HPO:probinson[2023-01-14]
OMIM:606072	Rippling muscle disease		HP:0003621	PMID:9537420	PCS		8/8			C	HPO:probinson[2023-01-14]
OMIM:606072	Rippling muscle disease		HP:0003760	OMIM:606072	IEA					P	HPO:iea[2009-02-17]
OMIM:606072	Rippling muscle disease		HP:0003391	PMID:9537420	PCS	HP:0003581	4/4			P	HPO:probinson[2023-01-14]
OMIM:606072	Rippling muscle disease		HP:0008981	PMID:9537420	PCS		8/8			P	HPO:probinson[2023-01-14]
OMIM:606072	Rippling muscle disease		HP:0003719	OMIM:606072	IEA					P	HPO:iea[2009-02-17]
OMIM:606072	Rippling muscle disease		HP:0003738	OMIM:606072	IEA					P	HPO:iea[2009-02-17]
OMIM:606072	Rippling muscle disease		HP:0003712	OMIM:606072	IEA					P	HPO:iea[2009-02-17]
OMIM:606072	Rippling muscle disease		HP:0003701	PMID:9537420	PCS		8/8			P	HPO:probinson[2023-01-14]
OMIM:606072	Rippling muscle disease		HP:0003559	OMIM:606072	IEA					P	HPO:iea[2009-02-17]
OMIM:606072	Rippling muscle disease		HP:0000006	PMID:9537420	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-02-19];HPO:probinson[2023-01-14]
OMIM:606072	Rippling muscle disease		HP:0003457	OMIM:606072	IEA					P	HPO:iea[2009-02-17]
OMIM:606072	Rippling muscle disease		HP:0003710	PMID:9537420	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-14]
OMIM:606072	Rippling muscle disease		HP:0008967	OMIM:606072	IEA					P	HPO:iea[2009-02-17]
OMIM:601709	Quebec platelet disorder		HP:0000132	OMIM:601709	TAS					P	HPO:probinson[2009-02-17]
OMIM:601709	Quebec platelet disorder		HP:0000978	OMIM:601709	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601709	Quebec platelet disorder		HP:0005261	OMIM:601709	TAS					P	HPO:probinson[2013-08-10]
OMIM:601709	Quebec platelet disorder		HP:0008148	OMIM:601709	IEA					P	HPO:iea[2009-02-17]
OMIM:601709	Quebec platelet disorder		HP:0000421	OMIM:601709	TAS					P	HPO:probinson[2009-02-17]
OMIM:601709	Quebec platelet disorder		HP:0001873	OMIM:601709	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601709	Quebec platelet disorder		HP:0000006	PMID:20007542	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-20]
OMIM:619146	Premature ovarian failure 17		HP:0008209	PMID:30489636	PCS		1/1			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619146	Premature ovarian failure 17		HP:0011969	PMID:30489636	PCS		1/1			P	HPO:probinson[2021-01-01]
OMIM:619146	Premature ovarian failure 17		HP:0011462	PMID:30489636	PCS		1/1			C	HPO:probinson[2021-01-01]
OMIM:619146	Premature ovarian failure 17		HP:0008232	PMID:30489636	PCS		1/1			P	HPO:probinson[2021-01-01]
OMIM:619146	Premature ovarian failure 17		HP:0031100	PMID:30489636	PCS		1/1			P	HPO:probinson[2021-01-01]
OMIM:619146	Premature ovarian failure 17		HP:0000007	PMID:30489636	PCS					I	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619146	Premature ovarian failure 17		HP:0008214	PMID:30489636	PCS		1/1			P	HPO:probinson[2021-01-01]
OMIM:619146	Premature ovarian failure 17		HP:0031103	PMID:30489636	PCS		1/1			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001298	OMIM:614462	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001250	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001252	PMID:22152680	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001290	OMIM:614462	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001270	PMID:22152680	PCS		1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002181	PMID:22152680	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002415	OMIM:614462	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0003128	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0003623	PMID:22152680	PCS		1/1			C	HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002059	OMIM:614462	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0000252	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002510	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0011968	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001263	PMID:22152680	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002151	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002093	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:6000829	PMID:24334290	PCS		2/2			P	HPO:probinson[2024-08-03]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0034392	PMID:22152680	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002928	PMID:22152680	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001639	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0000007	PMID:22152680	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001510	PMID:22152680	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0002104	OMIM:614462	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614462	Hyperglycinemia, lactic acidosis, and seizures		HP:0001336	OMIM:614462	TAS					P	HPO:skoehler[2017-07-13]
OMIM:153200	Lymphedema, hereditary, II		HP:0000175	OMIM:153200	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:153200	Lymphedema, hereditary, II		HP:0003550	OMIM:153200	TAS					P	HPO:probinson[2009-02-17]
OMIM:153200	Lymphedema, hereditary, II		HP:0000282	OMIM:153200	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:153200	Lymphedema, hereditary, II		HP:0011367	OMIM:153200	TAS		HP:0040283			P	HPO:probinson[2012-07-16]
OMIM:153200	Lymphedema, hereditary, II		HP:0003759	OMIM:153200	TAS					P	HPO:probinson[2009-02-17]
OMIM:153200	Lymphedema, hereditary, II		HP:0000006	OMIM:153200	TAS					I	HPO:probinson[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0001683	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0000175	OMIM:313850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0002323	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0002089	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0001669	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0000238	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0001539	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0002933	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0001417	OMIM:313850	IEA					I	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0001643	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0000047	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0000476	OMIM:313850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0000204	OMIM:313850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0000776	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:313850	Thoracoabdominal syndrome		HP:0000104	OMIM:313850	IEA					P	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0006956	OMIM:602200	IEA					P	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0000073	OMIM:602200	IEA					P	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0000086	OMIM:602200	IEA					P	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0000085	OMIM:602200	IEA					P	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0000007	OMIM:602200	IEA					I	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0000238	OMIM:602200	TAS					P	HPO:probinson[2012-06-03]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0002617	OMIM:602200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0002119	OMIM:602200	TAS					P	HPO:probinson[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0009777	OMIM:602200	IEA					P	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0003956	OMIM:602200	TAS					P	HPO:probinson[2012-06-03]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0009821	OMIM:602200	TAS					P	HPO:probinson[2012-06-03]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0003974	OMIM:602200	IEA					P	HPO:iea[2009-02-17]
OMIM:602200	Ventriculomegaly with defects of the radius and kidney		HP:0000104	OMIM:602200	IEA					P	HPO:iea[2009-02-17]
OMIM:612775	Cone-Rod dystrophy 9		HP:0000007	OMIM:612775	TAS					I	HPO:probinson[2013-04-07]
OMIM:612775	Cone-Rod dystrophy 9		HP:0000505	OMIM:612775	TAS	HP:0011463				P	HPO:probinson[2013-04-07]
OMIM:612775	Cone-Rod dystrophy 9		HP:0000548	OMIM:612775	TAS					P	HPO:probinson[2013-04-07]
OMIM:603678	Deafness, autosomal recessive 14		HP:0000407	PMID:9887371	PCS	HP:0003593				P	HPO:lccarmody[2019-01-29];HPO:lccarmody[2019-01-29]
OMIM:603678	Deafness, autosomal recessive 14		HP:0000007	OMIM:603678	TAS					I	HPO:skoehler[2017-07-13]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0001595	PMID:8673107	PCS		0/11			P	HPO:skoehler[2015-06-22];HPO:probinson[2024-03-10]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0001036	OMIM:604117	TAS					P	HPO:skoehler[2015-06-22]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0025114	OMIM:604117	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0009775	PMID:8673107	PCS		11/11			P	HPO:probinson[2022-12-15]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0007465	PMID:8673107	PCS		11/11			P	HPO:probinson[2022-12-15];HPO:probinson[2024-03-10]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0040162	OMIM:604117	TAS					P	HPO:skoehler[2015-06-22]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0000006	PMID:8673107	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-15]
OMIM:604117	Vohwinkel syndrome, variant form		HP:0000962	PMID:8673107	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2024-03-10]
OMIM:157700	Mitral valve prolapse 1		HP:0001519	OMIM:157700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:157700	Mitral valve prolapse 1		HP:0001065	OMIM:157700	TAS					P	HPO:probinson[2012-05-05]
OMIM:157700	Mitral valve prolapse 1		HP:0008433	OMIM:157700	IEA					P	HPO:iea[2009-02-17]
OMIM:157700	Mitral valve prolapse 1		HP:0000767	OMIM:157700	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:157700	Mitral valve prolapse 1		HP:0002705	OMIM:157700	TAS					P	HPO:skoehler[2015-12-30]
OMIM:157700	Mitral valve prolapse 1		HP:0000218	OMIM:157700	IEA					P	HPO:iea[2009-02-17]
OMIM:157700	Mitral valve prolapse 1		HP:0001653	OMIM:157700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:157700	Mitral valve prolapse 1		HP:0000006	OMIM:157700	IEA					I	HPO:iea[2009-02-17]
OMIM:157700	Mitral valve prolapse 1		HP:0001634	OMIM:157700	IEA					P	HPO:iea[2009-02-17]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0010529	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001256	PMID:34415117;PMID:30631761;PMID:31001818;PMID:27595554;PMID:31980904;PMID:26789910;PMID:31721432;PMID:38441608;PMID:24998929	PCS		14/44			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002342	PMID:34415117;PMID:30631761;PMID:31001818;PMID:27595554;PMID:31980904;PMID:26789910;PMID:24998929;PMID:38441608;PMID:31721432	PCS		14/43			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002021	PMID:31721432	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001250	PMID:30631761;PMID:31001818;PMID:31980904;PMID:24998929;PMID:32309624	PCS		7/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002187	PMID:30631761;PMID:34415117;PMID:31001818;PMID:27595554;PMID:31980904;PMID:26789910;PMID:24998929;PMID:31721432;PMID:38441608	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001252	PMID:34415117;PMID:31001818;PMID:31980904;PMID:26789910;PMID:24998929;PMID:31721432	PCS		9/39			P	HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0003593	PMID:30631761;PMID:34415117;PMID:31980904;PMID:26789910;PMID:38441608;PMID:32309624	PCS		7/12			C	HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0011856	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0003270	PMID:31980904;PMID:24998929	PCS		1/16			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0011410	PMID:31980904;PMID:24998929	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000716	PMID:31001818;PMID:24998929	PCS		2/24			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000957	PMID:31721432	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0011463	PMID:34415117;PMID:27595554	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000319	PMID:32309624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0011462	PMID:38441608	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000717	PMID:34415117;PMID:31001818;PMID:31980904;PMID:26789910;PMID:24998929;PMID:31721432;PMID:38441608	PCS		33/43			P	HPO:probinson[2022-08-13];HPO:probinson[2017-06-25];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0011461	PMID:31980904	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000316	PMID:34415117;PMID:31980904;PMID:24998929;PMID:38441608	PCS		11/18			P	HPO:probinson[2017-06-25];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0007325	PMID:34415117;PMID:38441608	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002019	PMID:31001818;PMID:27595554;PMID:31980904;PMID:24998929	PCS		12/28			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001763	PMID:24998929;PMID:31721432	PCS		4/19			P	HPO:probinson[2017-06-25];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000278	PMID:31721432	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001249	PMID:24998929;PMID:31721432;PMID:32309624	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000358	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002312	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000494	PMID:34415117;PMID:24998929;PMID:38441608;PMID:32309624	PCS		8/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002037	PMID:31980904;PMID:24998929	PCS		1/16			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000098	PMID:30631761;PMID:31001818;PMID:31980904;PMID:24998929;PMID:31721432;PMID:38441608	PCS		22/38			P	HPO:skoehler[2017-07-18];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002356	PMID:34415117;PMID:38441608	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0011968	PMID:34415117;PMID:38441608	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001263	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000053	PMID:31980904	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001065	PMID:31721432	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0100021	PMID:24998929;PMID:32309624	PCS		1/16			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0031354	PMID:31001818;PMID:27595554;PMID:24998929	PCS		11/24			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0031874	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:4000081	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0100023	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002904	PMID:31001818	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0032012	PMID:31001818;PMID:31980904	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0004209	PMID:31721432	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000565	PMID:31721432	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000400	PMID:31980904;PMID:31721432	PCS		5/14			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000006	PMID:24998929	PCS					I	HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000445	PMID:31980904;PMID:24998929;PMID:32309624	PCS		15/15			P	HPO:probinson[2017-06-25];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0006889	PMID:30631761;PMID:34415117;PMID:31001818;PMID:27595554;PMID:31980904;PMID:26789910;PMID:38441608;PMID:24998929	PCS		5/37			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:5200018	PMID:31980904	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000343	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002360	PMID:31980904;PMID:24998929	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001270	PMID:34415117;PMID:31001818;PMID:31980904;PMID:26789910;PMID:32309624	PCS		15/18			P	HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:4000073	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0100033	PMID:24998929	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0010864	PMID:30631761;PMID:34415117;PMID:31001818;PMID:27595554;PMID:31980904;PMID:26789910;PMID:38441608;PMID:31721432;PMID:24998929	PCS		6/43			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000739	PMID:31001818;PMID:31980904;PMID:26789910;PMID:24998929;PMID:38441608	PCS		11/30			P	HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000337	PMID:31980904	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000736	PMID:30631761;PMID:24998929	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002119	PMID:34415117;PMID:31001818;PMID:31980904;PMID:38441608	PCS		4/16			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0012171	PMID:31980904;PMID:26789910	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000256	PMID:34415117;PMID:30631761;PMID:31001818;PMID:31980904;PMID:26789910;PMID:24998929;PMID:31721432;PMID:38441608;PMID:32309624	PCS		33/46			P	HPO:probinson[2022-08-13];HPO:probinson[2017-06-25];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000336	PMID:34415117;PMID:31001818;PMID:31980904;PMID:24998929;PMID:31721432;PMID:38441608;PMID:32309624	PCS		29/40			P	HPO:probinson[2017-06-25];HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0006855	PMID:34415117;PMID:38441608	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002014	PMID:27595554;PMID:31980904;PMID:24998929	PCS		4/17			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0001561	PMID:31721432	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0025352	PMID:24998929	PCS					I	HPO:probinson[2017-06-25];HPO:probinson[2020-11-28]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000750	PMID:30631761;PMID:31001818;PMID:27595554;PMID:31980904;PMID:26789910;PMID:32309624	PCS		15/17			P	HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000431	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002376	PMID:31980904;PMID:26789910;PMID:24998929	PCS		10/20			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002373	PMID:24998929	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000194	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002451	PMID:34415117;PMID:38441608	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0400000	PMID:34415117;PMID:31980904;PMID:32309624	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000709	PMID:27595554;PMID:24998929;PMID:31721432	PCS		3/26			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0012760	PMID:31001818;PMID:31721432	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0002808	PMID:31721432	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000508	PMID:26789910	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000821	PMID:31001818	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0025502	PMID:30631761;PMID:31980904;PMID:24998929;PMID:38441608	PCS		3/20			P	HPO:probinson[2020-11-28];ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000307	PMID:26789910;PMID:24998929	PCS		11/11			P	HPO:probinson[2022-08-13];HPO:probinson[2017-06-25]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0100716	PMID:31001818;PMID:31980904	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0007018	PMID:31001818;PMID:31721432;PMID:24998929	PCS		7/33			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:615032	Intellectual developmental disorder with autism and macrocephaly		HP:0000303	PMID:34415117;PMID:38441608;PMID:32309624	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-08-20]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000582	PMID:19592390	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0002540	PMID:19592390	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000463	OMIM:613443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0001250	PMID:19592390	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0001252	PMID:19592390	PCS		5/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0003196	PMID:19592390	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0003593	PMID:19592390	PCS					C	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0001270	PMID:19592390	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000180	PMID:19592390	PCS		1/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000817	PMID:19592390	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000316	OMIM:613443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000954	PMID:19592390	PCS		1/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0002518	OMIM:613443	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000337	PMID:19592390	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000733	PMID:19592390	PCS		3/6			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0002119	PMID:19592390	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000219	PMID:19592390	PCS		1/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0002714	OMIM:613443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0025336	PMID:19592390	PCS		6/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0003745	OMIM:613443	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0006956	PMID:19592390	PCS		1/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0001344	PMID:19592390	PCS		6/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000331	PMID:19592390	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0031936	PMID:19592390	PCS		6/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0011968	PMID:19592390	PCS		1/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000490	PMID:19592390	PCS		2/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0002198	PMID:19592390	PCS		2/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0004691	PMID:19592390	PCS		2/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0005280	OMIM:613443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0200134	OMIM:613443	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0004209	PMID:19592390	PCS		1/6			P	HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000322	PMID:19592390	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0002500	OMIM:613443	TAS					P	HPO:skoehler[2013-03-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000006	PMID:19592390	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-08]
OMIM:613443	Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language		HP:0000369	OMIM:613443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308280	Impacted teeth, multiple		HP:0001571	OMIM:308280	IEA					P	HPO:iea[2009-02-17]
OMIM:308280	Impacted teeth, multiple		HP:0001417	OMIM:308280	IEA					I	HPO:iea[2009-02-17]
OMIM:308280	Impacted teeth, multiple		HP:0011069	OMIM:308280	IEA					P	HPO:iea[2009-02-17]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0002487	PMID:36055214	PCS		4/12			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000341	PMID:36055214	PCS		1/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0033407	PMID:36055214	PCS		1/11			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001250	PMID:36055214	PCS		10/15			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001272	PMID:36055214	PCS		1/6			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0002066	PMID:36055214	PCS		3/9			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001252	PMID:36055214	PCS		11/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0003593	PMID:36055214	PCS		14/18			C	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001251	PMID:36055214	PCS		7/9			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000639	PMID:36055214	PCS		7/13			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000518	PMID:36055214	PCS		5/11			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0011463	PMID:36055214	PCS		4/18			C	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0410309	PMID:36055214	PCS		1/11			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000218	PMID:36055214	PCS		1/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001249	PMID:36055214	PCS		7/8			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001348	PMID:36055214	PCS		4/10			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0003202	PMID:36055214	PCS		7/10			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001320	PMID:36055214	PCS		2/6			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0008619	PMID:36055214	PCS		11/14			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0002376	PMID:36055214	PCS		9/13			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0003487	PMID:36055214	PCS		4/9			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000276	PMID:36055214	PCS		1/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001263	PMID:36055214	PCS		17/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0002151	PMID:36055214	PCS		8/12			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0034008	PMID:36055214	PCS		4/6			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0009830	PMID:36055214	PCS		3/9			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000007	PMID:36055214	PCS					I	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000505	PMID:36055214	PCS		10/10			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000648	PMID:36055214	PCS		5/6			P	HPO:probinson[2022-11-25];HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001638	PMID:36055214	PCS		5/14			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0002505	PMID:36055214	PCS		6/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001698	PMID:36055214	PCS		3/11			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0001257	PMID:36055214	PCS		8/15			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000347	PMID:36055214	PCS		2/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0000369	PMID:36055214	PCS		1/18			P	HPO:probinson[2022-11-25]
OMIM:620089	Neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction		HP:0003535	PMID:36055214	PCS		5/11			P	HPO:probinson[2022-11-25]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0003577	PMID:33139725	PCS		1/3			C	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0001696	PMID:33139725	PCS		3/3			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0033036	PMID:33139725	PCS		0/2			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0010445	PMID:33139725	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0011577	PMID:33139725	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0011109	PMID:33139725	PCS		2/2			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0031590	PMID:33139725	PCS		1/1	MALE		P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0034011	PMID:33139725	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0000007	PMID:33139725	PCS					I	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0001748	PMID:33139725	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0000389	PMID:33139725	PCS		2/3			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0002247	PMID:33139725	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:619608	Heterotaxy, visceral, 11, autosomal, with male infertility		HP:0002566	PMID:33139725	PCS		1/3			P	HPO:probinson[2022-02-01]
OMIM:300804	Joubert syndrome 10		HP:0000286	OMIM:300804	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300804	Joubert syndrome 10		HP:0004325	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0003577	PMID:19800048	PCS		8/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0004322	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0001310	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0002002	PMID:19800048	PCS					P	HPO:probinson[2013-02-19]
OMIM:300804	Joubert syndrome 10		HP:0001156	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0001252	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0001270	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0002280	OMIM:300804	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300804	Joubert syndrome 10		HP:0025161	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0002719	PMID:19800048	PCS		9/9			P	HPO:probinson[2013-02-19]
OMIM:300804	Joubert syndrome 10		HP:0012471	OMIM:300804;PMID:19800048	PCS		12/12			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0002419	PMID:19800048	PCS		3/3			P	HPO:probinson[2013-02-19]
OMIM:300804	Joubert syndrome 10		HP:0008872	PMID:19800048	PCS					P	HPO:probinson[2013-02-19]
OMIM:300804	Joubert syndrome 10		HP:0000510	PMID:19800048	PCS		3/8			P	HPO:probinson[2013-02-19]
OMIM:300804	Joubert syndrome 10		HP:0000256	OMIM:300804	TAS		1/9			P	HPO:skoehler[2017-07-13]
OMIM:300804	Joubert syndrome 10		HP:0001007	PMID:19800048	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-24]
OMIM:300804	Joubert syndrome 10		HP:0001320	PMID:19800048	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:300804	Joubert syndrome 10		HP:0001561	PMID:19800048	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0000252	PMID:19800048	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0000494	OMIM:300804	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300804	Joubert syndrome 10		HP:0000431	PMID:19800048	PCS		1/1			P	HPO:probinson[2013-02-19]
OMIM:300804	Joubert syndrome 10		HP:0001344	PMID:19800048	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0001162	PMID:19800048	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0002591	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0001263	OMIM:300804	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300804	Joubert syndrome 10		HP:0033454	PMID:19800048	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0001419	PMID:19800048	PCS					I	HPO:probinson[2013-01-09]
OMIM:300804	Joubert syndrome 10		HP:0001954	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0000405	PMID:19800048	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0001830	PMID:19800048	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0002007	OMIM:300804	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300804	Joubert syndrome 10		HP:0001510	PMID:19800048	PCS					P	HPO:probinson[2013-02-19]
OMIM:300804	Joubert syndrome 10		HP:0001513	PMID:19800048	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300804	Joubert syndrome 10		HP:0000369	PMID:19800048	PCS		2/2			P	HPO:probinson[2013-02-19]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000286	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0002047	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0002089	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001371	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001373	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0009381	OMIM:253290	IEA				HP:0012828	P	HPO:probinson[2012-06-10]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000316	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0005905	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001989	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0002659	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000476	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001961	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000457	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000175	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001561	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001040	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000969	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0002948	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001999	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000007	OMIM:253290	TAS					I	HPO:skoehler[2012-10-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0001511	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0002304	OMIM:253290	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000883	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000347	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0000369	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:253290	Multiple pterygium syndrome, Lethal type		HP:0003634	OMIM:253290	IEA					P	HPO:iea[2009-02-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0010628	PMID:27569547	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0003577	PMID:27569547	PCS		4/5			C	HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0010307	PMID:27569547	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0003473	PMID:27569547	PCS		3/5			P	HPO:probinson[2022-10-17];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0001252	PMID:27569547	PCS		2/5			P	HPO:probinson[2022-10-17];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0003593	PMID:27569547	PCS		1/5			C	HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0001270	PMID:27569547	PCS		5/5			P	HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0001324	PMID:27569547	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0003701	PMID:27569547	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0000597	PMID:27569547	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0001763	PMID:27569547	PCS		1/5			P	HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0001249	PMID:27569547	PCS		3/5			P	HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0003202	PMID:27569547	PCS		1/5			P	HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0002015	PMID:27569547	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0002650	PMID:27569547	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0031936	PMID:27569547	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0001283	PMID:27569547	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0011968	PMID:27569547	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0002791	PMID:27569547	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0002033	PMID:27569547	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0001618	PMID:27569547	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0002808	PMID:27569547	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0000508	PMID:27569547	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0002804	PMID:27569547	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0000007	PMID:27569547	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0002104	PMID:27569547	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-17]
OMIM:617143	Myasthenic syndrome, congenital, 20, presynaptic		HP:0000467	PMID:27569547	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-17]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0000076	PMID:28381549	PCS		4/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0003577	PMID:28381549	PCS		1/7			C	HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0003621	PMID:28381549	PCS		1/7			C	HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0000089	PMID:28381549	PCS		2/7			P	HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0030674	PMID:28381549	PCS		2/7			C	HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0011463	PMID:28381549	PCS		2/7			C	HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0003584	PMID:28381549	PCS		1/7			C	HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0000086	PMID:28381549	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0003829	PMID:28381549	PCS					I	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0000003	PMID:28381549	PCS		1/7			P	HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0000006	PMID:28381549	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-06]
OMIM:618270	Congenital anomalies of kidney and urinary tract 3		HP:0000126	PMID:28381549	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:613325	Rhabdoid tumor predisposition syndrome 2		HP:0003593	PMID:20137775	PCS		2/2			C	HPO:probinson[2022-11-04]
OMIM:613325	Rhabdoid tumor predisposition syndrome 2		HP:0034401	PMID:10739764	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:613325	Rhabdoid tumor predisposition syndrome 2		HP:0034402	PMID:10739764	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:613325	Rhabdoid tumor predisposition syndrome 2		HP:0000006	PMID:20137775	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-04]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002982	OMIM:277440	TAS					P	HPO:probinson[2012-05-01]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002663	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002289	PMID:17970811	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:277440	Vitamin d-dependent rickets, type 2A		HP:0000286	PMID:17970811	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003698	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002980	OMIM:277440	TAS					P	HPO:probinson[2012-05-01]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000684	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003013	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Vitamin d-dependent rickets, type 2A		HP:0000365	PMID:17970811	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003155	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0001252	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003593	OMIM:277440	IEA					C	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0001290	OMIM:277440	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0001270	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0010502	OMIM:277440	TAS					P	HPO:probinson[2012-05-01]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0001508	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0009023	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000737	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0006297	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002979	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002757	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002753	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003106	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003029	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000951	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Vitamin d-dependent rickets, type 2A		HP:0003623	PMID:17970811	PCS		1/1			C	HPO:probinson[2022-03-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0005469	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002752	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000670	OMIM:277440	TAS					P	HPO:probinson[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002653	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002199	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000893	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Vitamin d-dependent rickets, type 2A		HP:0000431	PMID:17970811	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003025	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0001288	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003165	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0003020	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0004492	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0031415	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002748	PMID:17970811	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000007	PMID:17970811	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000867	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0001538	OMIM:277440	TAS					P	HPO:probinson[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002007	PMID:17970811	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0001510	OMIM:277440	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0002148	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:277440	Rickets, vitamin D-resistant, type IIA		HP:0000886	OMIM:277440	IEA					P	HPO:iea[2009-02-17]
OMIM:616249	Long QT syndrome 15		HP:0003621	PMID:24917665	PCS		1/5			C	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0001663	PMID:24917665;PMID:23388215	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0001662	PMID:24917665;PMID:23388215	PCS		4/6			P	HPO:probinson[2022-07-09];HPO:skoehler[2015-03-22];HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0001695	PMID:24917665;PMID:23388215	PCS		3/6			P	HPO:probinson[2022-07-09];HPO:skoehler[2015-03-22];HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0001250	PMID:24917665	PCS		1/5			P	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0030682	PMID:24917665	PCS		1/5			P	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0005184	PMID:24917665;PMID:23388215	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0034306	PMID:23388215	PCS		1/5			P	HPO:probinson[2022-09-05];HPO:probinson[2022-09-05]
OMIM:616249	Long QT syndrome 15		HP:0031677	PMID:24917665	PCS		1/5			P	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0034305	PMID:23388215	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:616249	Long QT syndrome 15		HP:0011463	PMID:24917665	PCS		3/5			C	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0011461	PMID:23388215	IEA		1/1			C	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0006682	PMID:24917665	PCS		2/5			P	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0001279	PMID:24917665	PCS		4/5			P	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0000006	PMID:23388215	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0001688	PMID:23388215	PCS		1/1			P	HPO:probinson[2022-07-09]
OMIM:616249	Long QT syndrome 15		HP:0003623	PMID:24917665	PCS		1/5			C	HPO:probinson[2022-07-09]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000286	PMID:26437029	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000483	PMID:26437029	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000486	PMID:26437029	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0002144	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0002188	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000089	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0004322	PMID:26437029	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001252	PMID:26437029	PCS		5/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0003196	PMID:26437029	PCS		3/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0002020	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0010049	PMID:26437029	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0012745	PMID:26437029	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0011335	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0011220	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000316	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000678	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000278	OMIM:617157	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001249	PMID:26437029	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001601	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000252	PMID:26437029	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000010	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0002035	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0011968	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000490	PMID:27718516	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001263	PMID:26437029	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0009891	PMID:27718516	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000007	PMID:26437029	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000964	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0009933	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0007359	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000960	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000248	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000384	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0003577	PMID:27718516	PCS		1/1			C	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000343	PMID:27718516	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000463	PMID:27718516;PMID:26437029	PCS		4/7			P	HPO:probinson[2023-02-23];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001156	PMID:26437029	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0008070	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0010743	PMID:26437029	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001508	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0009882	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000736	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000218	OMIM:617157	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000977	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000455	PMID:26437029	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0005989	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000852	PMID:26437029	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001561	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000750	PMID:26437029	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000233	PMID:27718516	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000431	PMID:26437029	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0031936	PMID:26437029	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0010819	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000272	PMID:26437029	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000470	PMID:27718516	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0011147	PMID:26437029	PCS		2/6			P	HPO:probinson[2023-02-23];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0011344	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0005280	PMID:27718516;PMID:26437029	PCS		2/7			P	HPO:probinson[2023-02-23];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000508	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0002967	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0002007	OMIM:617157	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001511	PMID:27718516	PCS		1/1			P	HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0001513	PMID:26437029	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617157	Short stature, brachydactyly, intellectual developmental disability, and seizures		HP:0000588	PMID:26437029	PCS		1/6			P	HPO:probinson[2023-02-23]
OMIM:618264	Mirror movements 4		HP:0001335	PMID:28945198	PCS					P	HPO:probinson[2019-06-13]
OMIM:618264	Mirror movements 4		HP:0000006	PMID:28945198	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:265050	3MC syndrome 2		HP:0003577	PMID:21258343	PCS		10/10			C	HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000365	PMID:21258343	PCS		6/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000486	OMIM:265050	IEA					P	HPO:iea[2009-02-17]
OMIM:265050	3MC syndrome 2		HP:0000581	OMIM:265050	IEA					P	HPO:iea[2009-02-17]
OMIM:265050	3MC syndrome 2		HP:0000085	OMIM:265050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:265050	3MC syndrome 2		HP:0000437	OMIM:265050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:265050	3MC syndrome 2		HP:0000316	PMID:21258343	PCS		10/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000337	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0009004	OMIM:265050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:265050	3MC syndrome 2		HP:0008897	PMID:21258343	PCS		7/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0002714	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0000537	OMIM:265050	IEA					P	HPO:iea[2009-02-17]
OMIM:265050	3MC syndrome 2		HP:0000218	PMID:21258343	PCS		2/10			P	HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0002678	PMID:21258343	PCS		6/10			P	HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0003468	OMIM:265050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:265050	3MC syndrome 2		HP:0001249	PMID:21258343	PCS		7/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0002996	PMID:21258343	PCS		4/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0002974	PMID:21258343	PCS		4/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0001540	PMID:21258343	PCS		4/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0002553	PMID:21258343	PCS		10/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000473	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0000175	PMID:21258343	PCS		4/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0001363	PMID:21258343	PCS		6/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000494	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0010759	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0000431	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0001382	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0001263	OMIM:265050	IEA					P	HPO:iea[2009-02-17]
OMIM:265050	3MC syndrome 2		HP:0005243	OMIM:265050	IEA					P	HPO:iea[2009-02-17]
OMIM:265050	3MC syndrome 2		HP:0000925	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0002827	OMIM:265050	IEA					P	HPO:iea[2009-02-17]
OMIM:265050	3MC syndrome 2		HP:0000508	PMID:21258343	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0002825	PMID:21258343	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000426	OMIM:265050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265050	3MC syndrome 2		HP:0000007	PMID:21258343	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000289	OMIM:265050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:265050	3MC syndrome 2		HP:0000047	OMIM:265050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:265050	3MC syndrome 2		HP:0000204	PMID:21258343	PCS		4/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-27]
OMIM:265050	3MC syndrome 2		HP:0000028	OMIM:265050	IEA					P	HPO:iea[2009-02-17]
OMIM:615026	Riboflavin deficiency		HP:0001254	PMID:29122468	PCS	HP:0003623	1/1			P	HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0002045	PMID:29122468	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0002033	OMIM:615026	IEA					P	HPO:skoehler[2015-08-23]
OMIM:615026	Riboflavin deficiency		HP:0001252	PMID:29122468	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0100504	PMID:29122468	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0001943	OMIM:615026	IEA					P	HPO:skoehler[2015-08-23]
OMIM:615026	Riboflavin deficiency		HP:0045045	PMID:29122468	PCS		1/1			P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0000006	PMID:29122468	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0003215	PMID:29122468	PCS		1/1			P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0001942	PMID:29122468	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-11]
OMIM:615026	Riboflavin deficiency		HP:0003128	PMID:29122468	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:261550	Persistent mullerian duct syndrome, types I and II		HP:0003577	PMID:11760020	PCS		2/2			C	HPO:probinson[2022-08-19]
OMIM:261550	Persistent mullerian duct syndrome, types I and II		HP:0000023	OMIM:261550	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-19]
OMIM:261550	Persistent mullerian duct syndrome, types I and II		HP:0003251	PMID:11760020	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-19]
OMIM:261550	Persistent mullerian duct syndrome, types I and II		HP:0000007	PMID:8162013	PCS					I	HPO:iea[2012-04-24]
OMIM:261550	Persistent mullerian duct syndrome, types I and II		HP:0031103	PMID:11760020	PCS		2/2			P	HPO:probinson[2022-08-19];HPO:probinson[2022-08-19]
OMIM:261550	Persistent mullerian duct syndrome, types I and II		HP:0008689	PMID:11760020	PCS		2/2	MALE		P	HPO:iea[2012-04-24];HPO:probinson[2022-08-19]
OMIM:614338	Pancreatic lipase deficiency		HP:0002630	PMID:24262094	PCS		2/2			P	HPO:probinson[2013-02-23];HPO:probinson[2023-04-18]
OMIM:614338	Pancreatic lipase deficiency		HP:0003146	PMID:24262094	PCS		2/2		HP:0012825	P	HPO:probinson[2023-04-18]
OMIM:614338	Pancreatic lipase deficiency		HP:0002570	PMID:24262094	PCS	HP:0003623	2/2			P	HPO:probinson[2013-02-23];HPO:probinson[2023-04-18]
OMIM:614338	Pancreatic lipase deficiency		HP:0000007	PMID:24262094	PCS					I	HPO:probinson[2012-10-17];HPO:probinson[2023-04-18]
OMIM:614338	Pancreatic lipase deficiency		HP:0012236	PMID:24262094	PCS		0/2			P	HPO:probinson[2023-04-18]
OMIM:614338	Pancreatic lipase deficiency		HP:0003623	PMID:24262094	PCS		2/2			C	HPO:probinson[2023-04-18]
OMIM:216900	Achromatopsia 2		HP:0000662	PMID:35456423	PCS		0/2			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0030465	PMID:35456423	PCS		2/2			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0011516	PMID:17265047	PCS		15/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0030825	PMID:17265047	PCS		1/16			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0030329	PMID:35456423	PCS		1/2			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0500041	PMID:35456423	PCS		2/2			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0500087	PMID:35456423	PCS		1/2			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0034362	PMID:17265047	PCS		6/16			P	HPO:probinson[2022-09-05]
OMIM:216900	Achromatopsia 2		HP:0012047	PMID:35456423	PCS		2/2			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0000639	PMID:35456423	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0011463	PMID:35456423	PCS		2/2			C	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0012043	PMID:17265047	PCS		4/16			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0000613	PMID:35456423	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0007750	PMID:17265047	PCS		5/16			P	HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0000007	PMID:9662398	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:216900	Achromatopsia 2		HP:0007663	PMID:17265047;PMID:35456423	PCS		17/17			P	HPO:probinson[2022-06-09]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002421	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000286	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002540	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002188	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001250	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000160	OMIM:613457	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0003196	PMID:33282601	PCS		1/9			P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001252	PMID:33282601	PCS		4/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0003593	PMID:33282601	PCS		1/9			C	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002020	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0012745	OMIM:613457	TAS					P	HPO:skoehler[2014-03-24]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0012741	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0033725	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000639	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000316	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0003508	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0003745	PMID:33282601	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001643	OMIM:613457	TAS		1/9			P	HPO:skoehler[2012-11-18]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000158	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0003623	PMID:33282601	PCS		9/9			C	HPO:probinson[2023-03-11];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000252	PMID:33282601	PCS		3/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001344	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002079	PMID:33282601	PCS		1/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002750	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002197	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0011968	PMID:33282601	PCS		3/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000490	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001263	PMID:33282601	PCS		3/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000648	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001257	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0008689	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000325	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000369	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001655	OMIM:613457	TAS		2/9			P	HPO:skoehler[2012-11-18]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001276	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000343	PMID:33282601	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0010627	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000023	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000540	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000581	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001274	PMID:33282601	PCS		3/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0010544	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001629	OMIM:613457	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001508	PMID:33282601	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001947	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0100704	PMID:33282601	PCS		1/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000817	OMIM:613457;PMID:33282601	PCS		11/19			P	HPO:probinson[2023-03-11];HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0030043	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000218	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001302	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001347	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0003027	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000431	PMID:33282601	PCS		2/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0005487	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0011344	PMID:33282601	PCS		3/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0100960	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0005280	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0002925	PMID:33282601	PCS		1/9			P	HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001319	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001357	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0001510	PMID:33282601	PCS		1/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000347	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613457	Chromosome 14q11-q22 deletion syndrome		HP:0000028	OMIM:613457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:115080	Cardiac conduction defectsudden cardiac death, included		HP:0011675	OMIM:115080	TAS					P	HPO:probinson[2009-02-17]
OMIM:115080	Cardiac conduction defectsudden cardiac death, included		HP:0001279	OMIM:115080	TAS					P	HPO:probinson[2009-02-17]
OMIM:115080	Cardiac conduction defectsudden cardiac death, included		HP:0000006	OMIM:115080	TAS					I	HPO:probinson[2009-02-17]
OMIM:115080	Cardiac conduction defectsudden cardiac death, included		HP:0001699	OMIM:115080	TAS					P	HPO:probinson[2009-02-17]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0033393	PMID:33472045	PCS		4/4			P	HPO:probinson[2021-04-27]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0001419	PMID:33472045	PCS					I	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0032560	PMID:33472045	PCS		4/4			P	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0003251	PMID:33472045	PCS		4/4			P	HPO:probinson[2021-04-27]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0012207	PMID:33472045	PCS		4/4			P	HPO:probinson[2021-04-27]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0032558	PMID:33472045	PCS		4/4			P	HPO:probinson[2021-04-27]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0000798	PMID:33472045	PCS		4/4			P	HPO:probinson[2021-04-27]
OMIM:301059	Spermatogenic failure, X-linked, 3		HP:0032559	PMID:33472045	PCS		4/4			P	HPO:probinson[2021-04-27]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001276	PMID:11733564	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000242	PMID:11733564	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0002521	PMID:11733564	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000486	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0003256	OMIM:609180	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001371	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001250	PMID:11733564	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000260	PMID:11733564	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001252	PMID:11733564	PCS		2/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001251	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0003593	PMID:11733564	PCS		1/3			C	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000958	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001508	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000639	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0002119	PMID:11733564	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001522	PMID:11733564	PCS		1/3			C	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0003623	PMID:11733564	PCS		2/3			C	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0002059	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000252	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001344	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000233	PMID:11733564	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0011968	PMID:11733564	PCS		1/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0011344	PMID:11733564	PCS		3/3			P	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000803	PMID:11733564	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0040189	OMIM:609180	TAS					P	HPO:skoehler[2015-10-05]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000007	PMID:11733564	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-26]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0001019	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000648	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:609180	Congenital disorder of glycosylation, type IF		HP:0000962	OMIM:609180	TAS					P	HPO:skoehler[2015-08-16]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0001760	PMID:32094424	PCS		1/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0003621	PMID:32094424	PCS		1/5			C	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0003401	PMID:32094424	PCS		1/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0002650	PMID:32094424	PCS		1/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0001288	PMID:32094424	PCS		5/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0003487	PMID:32094424	PCS		2/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0003484	PMID:32094424	PCS		0/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0001250	PMID:32094424	PCS		0/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0000020	PMID:32094424	PCS		0/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0002061	PMID:32094424	PCS		5/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0011448	PMID:32094424	PCS		4/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0007340	PMID:32094424	PCS		5/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0011462	PMID:32094424	PCS		4/5			C	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0002505	PMID:32094424	PCS	HP:0003584	2/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0000006	PMID:32094424	PCS					I	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0006986	PMID:32094424	PCS		0/5			P	HPO:probinson[2024-03-12]
OMIM:620512	Spastic paraplegia 18A, autosomal dominant		HP:0001249	PMID:32094424	PCS		0/5			P	HPO:probinson[2024-03-12]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001773	PMID:18413476	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001156	OMIM:275900	TAS					P	HPO:skoehler[2014-11-26]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001310	PMID:18413476	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0004322	OMIM:275900	TAS					P	HPO:probinson[2012-04-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001272	OMIM:275900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0003693	PMID:18413476	PCS		2/2			P	HPO:probinson[2012-04-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001371	OMIM:275900	IEA					P	HPO:iea[2009-02-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0002064	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0002061	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001270	PMID:18413476	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0000639	PMID:18413476	PCS		0/2			P	HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0011463	PMID:18413476	PCS		2/2			C	HPO:probinson[2012-04-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0012371	OMIM:275900	TAS					P	HPO:skoehler[2013-05-31]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0007340	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0009487	PMID:18413476	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0012450	PMID:18413476	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0000712	OMIM:275900	IEA					P	HPO:iea[2009-02-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0000316	OMIM:275900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0030084	OMIM:275900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0002313	OMIM:275900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001765	OMIM:275900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001347	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0002751	PMID:18413476	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0002015	PMID:18413476	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0003487	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001288	OMIM:275900	TAS					P	HPO:probinson[2012-04-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001761	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0000012	PMID:20301556	TAS					P	HPO:probinson[2023-04-09]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001260	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0006938	PMID:18413476	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001263	OMIM:275900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0011449	OMIM:275900	TAS					P	HPO:probinson[2012-04-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0011448	OMIM:275900	TAS					P	HPO:probinson[2012-04-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0012385	OMIM:275900	TAS					P	HPO:skoehler[2013-10-22]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001317	OMIM:275900	IEA					P	HPO:iea[2009-02-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0000007	PMID:18413476	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0002307	OMIM:275900	IEA					P	HPO:iea[2009-02-17]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0005639	PMID:18413476	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0001258	PMID:18413476	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:275900	Spastic paraplegia 20, autosomal recessive		HP:0006986	OMIM:275900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:202550	Aganglionosis, total intestinal		HP:0005241	OMIM:202550	IEA					P	HPO:iea[2009-02-17]
OMIM:202550	Aganglionosis, total intestinal		HP:0000007	OMIM:202550	IEA					I	HPO:iea[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000483	OMIM:203100	TAS					P	HPO:skoehler[2010-06-20]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0003577	OMIM:203100	TAS					C	HPO:skoehler[2012-10-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0001022	OMIM:203100	IEA					P	HPO:skoehler[2015-01-27]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0005599	OMIM:203100	TAS					P	HPO:probinson[2013-02-25]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000486	OMIM:203100	TAS					P	HPO:skoehler[2013-02-25]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000639	OMIM:203100	TAS					P	HPO:probinson[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0011364	OMIM:203100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000539	OMIM:203100	TAS					P	HPO:probinson[2013-02-25]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000613	OMIM:203100	TAS					P	HPO:probinson[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000635	OMIM:203100	TAS					P	HPO:probinson[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0007750	OMIM:203100	TAS					P	HPO:iea[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000007	OMIM:203100	TAS					I	HPO:skoehler[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0001107	OMIM:203100	TAS					P	HPO:probinson[2012-07-19]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0007663	OMIM:203100	TAS					P	HPO:skoehler[2015-07-26]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000505	OMIM:203100	TAS					P	HPO:probinson[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0200098	OMIM:203100	TAS					P	HPO:skoehler[2013-06-05]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000545	OMIM:203100	TAS					P	HPO:probinson[2009-02-17]
OMIM:203100	Albinism, oculocutaneous, type IA		HP:0000577	OMIM:203100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0002919	PMID:16697227	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0001508	PMID:16697227	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0012120	PMID:16697227;PMID:16752391	PCS		2/2		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0003593	PMID:16697227;PMID:16752391	PCS		2/2			C	HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0002020	PMID:16697227	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0001944	PMID:16697227	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0002160	PMID:16697227	PCS		0/1			P	HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0000007	PMID:16752391	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0001270	PMID:16752391	PCS		1/1			P	HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0031544	PMID:16752391	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0001257	PMID:16752391	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:251120	Methylmalonyl-Coa epimerase deficiency		HP:0001942	PMID:16697227	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:604498	Amegakaryocytic thrombocytopenia, congenital		HP:0001320	OMIM:604498	TAS					P	HPO:probinson[2009-02-17]
OMIM:604498	Amegakaryocytic thrombocytopenia, congenital		HP:0000007	OMIM:604498	TAS					I	HPO:probinson[2009-02-17]
OMIM:604498	Amegakaryocytic thrombocytopenia, congenital		HP:0004859	OMIM:604498	TAS					P	HPO:probinson[2009-02-17]
OMIM:604498	Amegakaryocytic thrombocytopenia, congenital		HP:0001873	OMIM:604498	IEA					P	HPO:probinson[2009-02-17]
OMIM:604498	Amegakaryocytic thrombocytopenia, congenital		HP:0001876	OMIM:604498	TAS					P	HPO:probinson[2009-02-17]
OMIM:604498	Amegakaryocytic thrombocytopenia, congenital		HP:0005548	OMIM:604498	TAS					P	HPO:probinson[2009-02-17]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002421	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0010307	PMID:23814038	PCS		2/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0030774	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001252	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0012707	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002240	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002020	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0031964	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001508	PMID:23814038	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0003648	PMID:23814038	PCS		2/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001946	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001942	PMID:23814038	PCS		2/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001403	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0003623	PMID:23814038	PCS		2/2			C	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0003128	PMID:23814038	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0031956	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002098	PMID:23814038	PCS	HP:0003623	2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002098	PMID:23814038	PCS		2/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002395	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0011968	PMID:23814038	PCS		1/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002033	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0002490	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0030948	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0032988	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0000007	PMID:23814038	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001319	PMID:23814038	PCS					P	HPO:skoehler[2014-02-06];HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001612	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0001414	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:615595	Combined oxidative phosphorylation deficiency 19		HP:0003557	PMID:23814038	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:616922	Striatal degeneration, autosomal dominant 2		HP:0001300	PMID:27058447	PCS					P	HPO:probinson[2017-06-23]
OMIM:616922	Striatal degeneration, autosomal dominant 2		HP:0003680	OMIM:616922	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616922	Striatal degeneration, autosomal dominant 2		HP:0002072	PMID:27058447	PCS					P	HPO:probinson[2017-06-23]
OMIM:616922	Striatal degeneration, autosomal dominant 2		HP:0010994	PMID:27058447	PCS					P	HPO:probinson[2017-06-23]
OMIM:616922	Striatal degeneration, autosomal dominant 2		HP:0001268	PMID:27058447	PCS					P	HPO:probinson[2017-06-23]
OMIM:616922	Striatal degeneration, autosomal dominant 2		HP:0000006	PMID:27058447	PCS					I	HPO:probinson[2017-06-23]
OMIM:616922	Striatal degeneration, autosomal dominant 2		HP:0001249	PMID:27058447	PCS					P	HPO:probinson[2017-06-23]
OMIM:611095	Intellectual developmental disorder, autosomal recessive 9/26		HP:0000007	OMIM:611095	TAS					I	HPO:probinson[2015-05-10]
OMIM:611095	Intellectual developmental disorder, autosomal recessive 9/26		HP:0001270	OMIM:611095	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611095	Intellectual developmental disorder, autosomal recessive 9/26		HP:0001510	OMIM:611095	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611095	Intellectual developmental disorder, autosomal recessive 9/26		HP:0001257	OMIM:611095	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611095	Intellectual developmental disorder, autosomal recessive 9/26		HP:0001249	OMIM:611095	TAS					P	HPO:probinson[2015-05-10]
OMIM:311510	Waisman syndrome		HP:0002465	OMIM:311510	TAS					P	HPO:skoehler[2015-02-22]
OMIM:311510	Waisman syndrome		HP:0002322	PMID:26399558	PCS		6/7			P	HPO:probinson[2012-07-18];HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0002067	PMID:26399558	PCS		7/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0001355	OMIM:311510	TAS					P	HPO:probinson[2009-02-17]
OMIM:311510	Waisman syndrome		HP:0003596	PMID:26399558	PCS		5/7			C	HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0001300	PMID:26399558	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0001250	OMIM:311510	TAS					P	HPO:probinson[2009-02-17]
OMIM:311510	Waisman syndrome		HP:0002362	OMIM:311510	TAS					P	HPO:probinson[2009-02-17]
OMIM:311510	Waisman syndrome		HP:0002396	OMIM:311510	TAS					P	HPO:probinson[2009-02-17]
OMIM:311510	Waisman syndrome		HP:0001260	OMIM:311510	TAS					P	HPO:skoehler[2015-02-22]
OMIM:311510	Waisman syndrome		HP:0001263	OMIM:311510	TAS					P	HPO:skoehler[2015-02-22]
OMIM:311510	Waisman syndrome		HP:0002063	PMID:26399558	PCS		7/7			P	HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0002172	PMID:26399558	PCS		5/7			P	HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0100660	OMIM:311510	TAS					P	HPO:skoehler[2015-02-22]
OMIM:311510	Waisman syndrome		HP:0100315	OMIM:311510	IEA					P	HPO:skoehler[2018-10-08]
OMIM:311510	Waisman syndrome		HP:0000726	OMIM:311510	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:311510	Waisman syndrome		HP:0001419	PMID:26399558	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0011462	PMID:26399558	PCS		2/7			C	HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0002548	PMID:26399558	PCS		6/6			P	HPO:probinson[2022-11-10]
OMIM:311510	Waisman syndrome		HP:0002007	OMIM:311510	TAS					P	HPO:probinson[2009-02-17]
OMIM:311510	Waisman syndrome		HP:0000256	OMIM:311510	TAS					P	HPO:skoehler[2015-02-22]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0002023	PMID:14872406	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0002089	OMIM:273395	IEA					P	HPO:iea[2009-02-17]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0003057	PMID:14872406	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000068	PMID:14872406	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000782	PMID:14872406	PCS		0/3			P	HPO:probinson[2024-03-09]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0001195	PMID:14872406	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000042	PMID:14872406	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000518	PMID:14872406	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0011461	PMID:14872406	PCS		4/4			C	HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0001746	PMID:14872406	PCS		1/3			P	HPO:probinson[2014-05-24];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0008697	PMID:14872406	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000238	OMIM:273395	IEA					P	HPO:iea[2009-02-17]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0001543	PMID:14872406	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000776	PMID:14872406	PCS		1/3			P	HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000175	PMID:14872406	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000453	PMID:14872406	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0008839	PMID:14872406	PCS		2/3			P	HPO:probinson[2014-05-24];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0011743	PMID:14872406	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000007	PMID:14872406	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000568	PMID:14872406	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000889	PMID:14872406	PCS		0/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-09]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0009932	PMID:14872406	PCS		1/3			P	HPO:probinson[2014-05-24];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000204	PMID:14872406	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000369	OMIM:273395	IEA					P	HPO:iea[2009-02-17]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000347	OMIM:273395	IEA					P	HPO:iea[2009-02-17]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0005316	OMIM:273395	IEA					P	HPO:iea[2009-02-17]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000104	PMID:14872406	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:273395	Tetraamelia, autosomal recessive		HP:0000148	PMID:14872406	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-25]
OMIM:179600	Raynaud disease		HP:0000924	OMIM:179600	IEA					P	HPO:iea[2009-02-17]
OMIM:179600	Raynaud disease		HP:0030880	OMIM:179600	TAS					P	HPO:skoehler[2017-07-13]
OMIM:179600	Raynaud disease		HP:0000006	OMIM:179600	IEA					I	HPO:iea[2009-02-17]
OMIM:303100	Choroideremia		HP:0001133	PMID:17698759	PCS	HP:0003596	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0003621	PMID:17698759;PMID:24913019	PCS		4/10			C	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0007737	PMID:24913019	PCS		3/6			P	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0007814	PMID:24913019	PCS		1/6			P	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0000662	PMID:17698759;PMID:24913019	PCS		10/10			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0000580	PMID:17698759	PCS		4/4			P	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0030505	PMID:17698759	PCS		1/4			P	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0000529	PMID:17698759	PCS	HP:0003596	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0011463	PMID:17698759;PMID:24913019	PCS		6/10			C	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0007793	PMID:17698759	PCS		1/4			P	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0007894	PMID:17698759	PCS		4/4			P	HPO:probinson[2022-03-16];HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0000505	PMID:17698759;PMID:24913019	PCS		10/10			P	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0001417	PMID:1598901	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0200065	PMID:17698759	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0007843	PMID:24913019	PCS		4/6			P	HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0001139	PMID:17698759	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:303100	Choroideremia		HP:0000533	PMID:17698759	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-16]
OMIM:614847	Epilepsy, idiopathic generalized, susceptibility to, 12		HP:0002069	OMIM:614847	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614847	Epilepsy, idiopathic generalized, susceptibility to, 12		HP:0003828	OMIM:614847	TAS					M	HPO:skoehler[2017-07-13]
OMIM:614847	Epilepsy, idiopathic generalized, susceptibility to, 12		HP:0003829	OMIM:614847	TAS					I	HPO:skoehler[2012-11-16]
OMIM:614847	Epilepsy, idiopathic generalized, susceptibility to, 12		HP:0000006	OMIM:614847	TAS					I	HPO:skoehler[2012-11-16]
OMIM:614847	Epilepsy, idiopathic generalized, susceptibility to, 12		HP:0001249	OMIM:614847	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:301071	Thrombophilia 13, X-linked, due to factor VIII defect		HP:0003581	PMID:33275657	PCS		7/7			C	HPO:probinson[2022-03-28]
OMIM:301071	Thrombophilia 13, X-linked, due to factor VIII defect		HP:0002625	PMID:33275657	PCS		7/7			P	HPO:probinson[2022-03-28]
OMIM:301071	Thrombophilia 13, X-linked, due to factor VIII defect		HP:0001423	PMID:33275657	PCS					I	HPO:probinson[2022-03-28]
OMIM:301071	Thrombophilia 13, X-linked, due to factor VIII defect		HP:0030977	PMID:33275657	PCS		7/7			P	HPO:probinson[2022-04-10]
OMIM:301071	Thrombophilia 13, X-linked, due to factor VIII defect		HP:0002204	PMID:33275657	PCS		4/7			P	HPO:probinson[2022-03-28]
OMIM:130200	Electroencephalographic peculiarity: 14 and 6 per sec. positive spikephenomenon		HP:0002353	OMIM:130200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:130200	Electroencephalographic peculiarity: 14 and 6 per sec. positive spikephenomenon		HP:0000006	OMIM:130200	IEA					I	HPO:iea[2009-02-17]
OMIM:617396	Anauxetic dysplasia 2		HP:0001792	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0003577	PMID:21455487	PCS		2/2			C	HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0001156	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0004322	OMIM:617396	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617396	Anauxetic dysplasia 2		HP:0001371	OMIM:617396	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617396	Anauxetic dysplasia 2		HP:0002164	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0002680	PMID:21455487	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0004482	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0100255	PMID:21455487	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0010646	PMID:21455487	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0008070	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0100864	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0000914	OMIM:617396	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617396	Anauxetic dysplasia 2		HP:0002812	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0003307	OMIM:617396	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617396	Anauxetic dysplasia 2		HP:0000158	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0003423	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0002673	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0002750	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0003300	PMID:21455487	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0000470	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0011800	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0000668	OMIM:617396	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0008444	PMID:21455487	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0000007	PMID:21455487	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0002967	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0001511	PMID:21455487	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:617396	Anauxetic dysplasia 2		HP:0008802	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617396	Anauxetic dysplasia 2		HP:0008824	OMIM:617396	TAS					P	HPO:skoehler[2017-07-13]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000121	PMID:23434854	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-22]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000705	PMID:21549343	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-22]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000083	OMIM:204690	IEA					P	HPO:iea[2009-02-17]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000805	OMIM:204690	IEA					P	HPO:iea[2009-02-17]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0001548	OMIM:204690	IEA					P	HPO:skoehler[2010-06-20]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000007	PMID:21549343	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-22]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0004727	OMIM:204690	IEA					P	HPO:iea[2009-02-17]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000103	OMIM:204690	IEA					P	HPO:iea[2009-02-17]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0006302	OMIM:204690	IEA					P	HPO:iea[2009-02-17]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000169	PMID:21549343	PCS		4/4			P	HPO:probinson[2022-06-22]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000696	PMID:21549343	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-22]
OMIM:204690	Amelogenesis imperfecta, type IG (enamel-renal syndrome)		HP:0000212	PMID:21990045	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-22]
OMIM:148350	Keratoderma, palmoplantar, with deafness		HP:0000365	OMIM:148350	IEA	HP:0011463				P	HPO:skoehler[2010-06-20]
OMIM:148350	Keratoderma, palmoplantar, with deafness		HP:0000972	OMIM:148350	IEA					P	HPO:iea[2009-02-17]
OMIM:148350	Keratoderma, palmoplantar, with deafness		HP:0000006	OMIM:148350	IEA					I	HPO:iea[2009-02-17]
OMIM:616063	Porokeratosis 8, disseminated superficial Actinic type		HP:0003621	PMID:25180256	PCS					C	HPO:probinson[2022-04-12]
OMIM:616063	Porokeratosis 8, disseminated superficial Actinic type		HP:0011462	PMID:25180256	PCS					C	HPO:probinson[2022-04-12]
OMIM:616063	Porokeratosis 8, disseminated superficial Actinic type		HP:0200034	PMID:25180256	PCS					P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616063	Porokeratosis 8, disseminated superficial Actinic type		HP:0200044	PMID:25180256	PCS					P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616063	Porokeratosis 8, disseminated superficial Actinic type		HP:0000006	PMID:25180256	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:619350	Visceral myopathy 2		HP:0002036	PMID:31389005	PCS		5/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0000021	PMID:31389005	PCS		5/7			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0002015	PMID:31389005	PCS		3/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0030996	PMID:31389005	PCS		1/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0031857	PMID:31389005	PCS		2/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0005214	PMID:31389005	PCS		1/7			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0004389	PMID:31389005	PCS		1/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0002035	PMID:31389005	PCS		1/7			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0002043	PMID:31389005	PCS		1/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0002580	PMID:31389005	PCS		1/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0002020	PMID:31389005	PCS		5/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0100580	PMID:31389005	PCS		1/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0100633	PMID:31389005	PCS		5/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0033165	PMID:31389005	PCS		1/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0012450	PMID:31389005	PCS		1/8			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0000006	PMID:31389005	PCS					I	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0002566	PMID:31389005	PCS		1/7			P	HPO:probinson[2021-06-28]
OMIM:619350	Visceral myopathy 2		HP:0002578	PMID:31389005	PCS		2/8			P	HPO:probinson[2021-06-28]
OMIM:605779	Nail disorder, nonsyndromic congenital, 7		HP:0002164	OMIM:605779	TAS					P	HPO:probinson[2009-02-17]
OMIM:605779	Nail disorder, nonsyndromic congenital, 7		HP:0030803	OMIM:605779	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605779	Nail disorder, nonsyndromic congenital, 7		HP:0001598	OMIM:605779	TAS					P	HPO:probinson[2009-02-17]
OMIM:605779	Nail disorder, nonsyndromic congenital, 7		HP:0000006	OMIM:605779	IEA					I	HPO:iea[2009-02-17]
OMIM:614674	Periodic fever, menstrual cycle-dependent		HP:0002076	OMIM:614674	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614674	Periodic fever, menstrual cycle-dependent		HP:0200067	OMIM:614674	TAS		HP:0040283			H	HPO:skoehler[2013-05-31]
OMIM:614674	Periodic fever, menstrual cycle-dependent		HP:0001945	OMIM:614674	IEA					P	HPO:skoehler[2015-08-05]
OMIM:614674	Periodic fever, menstrual cycle-dependent		HP:0003118	OMIM:614674	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614674	Periodic fever, menstrual cycle-dependent		HP:0000006	OMIM:614674	TAS					I	HPO:skoehler[2012-10-17]
OMIM:105250	Amyloidosis, primary localized cutaneous, 1		HP:0000958	OMIM:105250	TAS					P	HPO:skoehler[2018-10-08]
OMIM:105250	Amyloidosis, primary localized cutaneous, 1		HP:0100725	PMID:18179886	PCS	HP:0011463	16/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-06]
OMIM:105250	Amyloidosis, primary localized cutaneous, 1		HP:0012309	PMID:18179886	PCS		16/16			P	HPO:probinson[2024-03-06]
OMIM:105250	Amyloidosis, primary localized cutaneous, 1		HP:0011463	PMID:18179886	PCS		16/16			C	HPO:probinson[2024-03-06]
OMIM:105250	Amyloidosis, primary localized cutaneous, 1		HP:0040189	OMIM:105250	TAS					P	HPO:skoehler[2018-10-08]
OMIM:105250	Amyloidosis, primary localized cutaneous, 1		HP:0000989	OMIM:105250	TAS		16/16			P	HPO:probinson[2009-02-17]
OMIM:105250	Amyloidosis, primary localized cutaneous, 1		HP:0000006	PMID:18179886	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-06]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0000431	OMIM:612563	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0004322	OMIM:612563	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0003196	OMIM:612563	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0000316	OMIM:612563	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0005518	PMID:19061985	PCS		1/1			P	HPO:probinson[2013-03-01]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0001972	PMID:19061985	PCS		1/1			P	HPO:probinson[2013-03-01]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0001510	OMIM:612563	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0000006	PMID:19061985	PCS		1/1			I	HPO:probinson[2013-01-09]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0000215	OMIM:612563	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612563	Diamond-Blackfan anemia 8		HP:0001875	OMIM:612563	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000286	PMID:14598339	PCS		1/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001770	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001374	PMID:14598339	PCS		1/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001377	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000046	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000486	PMID:14598339	PCS		5/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001212	PMID:14598339	PCS		1/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0004322	PMID:14598339	PCS		7/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001250	PMID:14598339	PCS		4/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001252	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001290	OMIM:609625	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000319	PMID:14598339	PCS		2/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000718	PMID:14598339	PCS		4/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0002938	PMID:14598339	PCS		1/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000316	PMID:14598339	PCS		2/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001328	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000954	PMID:14598339	PCS		3/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0009466	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0008897	OMIM:609625	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000752	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001643	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0003745	OMIM:609625	IEA					I	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001249	OMIM:609625	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000494	PMID:14598339	PCS		1/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000252	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000054	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001263	PMID:14598339	PCS		7/15			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000407	OMIM:609625	TAS					P	HPO:skoehler[2015-12-30]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000448	PMID:14598339	PCS		10/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000767	PMID:14598339	PCS		1/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001539	PMID:14598339	PCS		1/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0004209	PMID:14598339	PCS		7/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000444	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001852	PMID:14598339	PCS		2/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000006	PMID:14598339	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000369	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000325	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000324	OMIM:609625	IEA		8/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001792	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000582	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000343	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0002162	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0003691	PMID:14598339	PCS		1/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001270	PMID:14598339	PCS		9/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0005709	PMID:14598339	PCS		3/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000736	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000219	PMID:14598339	PCS		6/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000218	PMID:14598339	PCS		1/15			P	HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000411	PMID:14598339	PCS		4/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0006610	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000454	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0002136	OMIM:609625	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001363	OMIM:609625	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000076	PMID:14598339	PCS		2/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000750	PMID:14598339	PCS		8/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000431	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000470	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001518	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000268	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0002007	OMIM:609625	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0001631	PMID:14598339	PCS		2/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000465	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000028	PMID:14598339	PCS		2/2	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:609625	Chromosome 10q26 deletion syndrome		HP:0000347	OMIM:609625	IEA					P	HPO:iea[2009-02-17]
OMIM:616705	Deafness, autosomal recessive 97		HP:0000407	PMID:25941349	PCS	HP:0003593	9/9			P	HP:probinson[2019-03-02]
OMIM:616705	Deafness, autosomal recessive 97		HP:0000007	PMID:25941349	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0012265	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0000365	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0002110	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0032341	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0032342	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0000007	PMID:28543983	PCS					I	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0000403	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0012207	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0006532	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619436	Ciliary dyskinesia, primary, 46		HP:0011108	PMID:28543983	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0003510	PMID:31630789	PCS		4/4			P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0003026	PMID:31630789	PCS		4/4			P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0002650	PMID:31630789	PCS		1/4			P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0002970	PMID:31630789	PCS		4/4			P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0003850	PMID:31630789	PCS					P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0003051	PMID:31630789	PCS					P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0006361	PMID:31630789	PCS					P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0001903	PMID:31630789	PCS		0/4			P	HPO:probinson[2020-04-24];HPO:probinson[2024-03-16]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0000926	PMID:31630789	PCS		4/4			P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0008897	PMID:31630789	PCS	HP:0003593				P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0002812	PMID:31630789	PCS		4/4			P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0030291	PMID:31630789	PCS					P	HPO:probinson[2020-04-24]
OMIM:618728	Spondyloepimetaphyseal dysplasia, Isidor-Toutain type		HP:0000006	PMID:31630789	PCS					I	HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:610374	Diabetes mellitus, transient neonatal 2		HP:0008255	PMID:16885549	PCS	HP:0003623				P	HPO:probinson[2013-01-09]
OMIM:610374	Diabetes mellitus, transient neonatal 2		HP:0005978	PMID:16885549	PCS	HP:0003581	2/7			P	HPO:probinson[2013-04-01]
OMIM:610374	Diabetes mellitus, transient neonatal 2		HP:0000006	PMID:16885549	PCS					I	HPO:probinson[2013-04-01]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001298	PMID:34161705	PCS		3/10			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000486	PMID:34161705	PCS		7/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001332	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001250	PMID:34161705	PCS		2/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001251	PMID:34161705	PCS		11/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0003593	PMID:34161705	PCS					C	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000319	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0004619	PMID:34161705	PCS		1/10			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000218	PMID:34161705	PCS		3/12			P	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001324	PMID:34161705	PCS		5/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000212	PMID:34161705	PCS		2/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000278	PMID:34161705	PCS		2/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0008936	PMID:34161705	PCS		4/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0003763	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0002015	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0002059	PMID:34161705	PCS		4/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001344	PMID:34161705	PCS		2/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000750	PMID:34161705	PCS		4/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0008619	PMID:34161705	PCS		2/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0031936	PMID:34161705	PCS		10/10			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000276	PMID:34161705	PCS		3/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001761	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001266	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001321	PMID:34161705	PCS		7/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0011968	PMID:34161705	PCS		1/12		HP:0012828	P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001260	PMID:34161705	PCS		3/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0034007	PMID:34161705	PCS		7/12			P	HPO:probinson[2021-10-03]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0100660	PMID:34161705	PCS		2/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0100753	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0003819	PMID:34161705	PCS		1/12			C	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000729	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000508	PMID:34161705	PCS		2/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000767	PMID:34161705	PCS		2/10			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000007	PMID:34161705	TAS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000648	PMID:34161705	PCS		7/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0004209	PMID:34161705	PCS		3/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000488	PMID:34161705	PCS		2/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001510	PMID:34161705	PCS		3/8			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001337	PMID:34161705	PCS		8/11			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0001611	PMID:34161705	PCS		2/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000544	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:619422	Spinocerebellar ataxia, autosomal recessive 31		HP:0000742	PMID:34161705	PCS		1/12			P	HPO:probinson[2021-08-22]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0003577	PMID:20381006	PCS		12/12			C	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000089	PMID:20381006	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000086	PMID:20381006	PCS		2/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0010055	PMID:20381006	PCS		1/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0011220	PMID:20381006	PCS		9/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0002937	PMID:20381006	PCS		1/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0006297	PMID:20381006	PCS		2/10			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000316	PMID:20381006	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0006357	PMID:20381006	PCS		2/7			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0009701	PMID:20381006	PCS		11/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0001642	PMID:20381006	PCS		1/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0002974	PMID:20381006	PCS		7/10			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000494	PMID:20381006	PCS		4/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0002650	PMID:20381006	PCS		1/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0003022	PMID:20381006	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000272	PMID:20381006	PCS		7/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0002194	PMID:20381006	PCS		1/10			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000668	PMID:20381006	PCS		1/10			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000767	PMID:20381006	PCS		1/12			P	HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000007	PMID:20381006	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0001159	PMID:20381006	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000347	PMID:20381006	PCS		6/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0002984	PMID:20381006	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0000104	PMID:20381006	PCS		4/12			P	HPO:skoehler[2013-04-18];HPO:probinson[2022-12-15]
OMIM:212780	Cenani-Lenz syndactyly syndrome		HP:0001798	PMID:20381006	PCS		11/12			P	HPO:probinson[2022-12-15]
OMIM:245800	Laurence-Moon syndrome		HP:0001155	OMIM:245800	IEA					P	HPO:iea[2009-02-17]
OMIM:245800	Laurence-Moon syndrome		HP:0000054	OMIM:245800	IEA					P	HPO:iea[2009-02-17]
OMIM:245800	Laurence-Moon syndrome		HP:0000046	OMIM:245800	IEA					P	HPO:iea[2009-02-17]
OMIM:245800	Laurence-Moon syndrome		HP:0004322	PMID:25480986	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0000580	OMIM:245800	IEA					P	HPO:iea[2009-02-17]
OMIM:245800	Laurence-Moon syndrome		HP:0001251	PMID:25480986	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0010442	PMID:25480986	PCS		0/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0000639	PMID:25480986	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0009830	PMID:25480986	PCS		3/4			P	HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0000007	PMID:25480986	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0001258	OMIM:245800	IEA					P	HPO:iea[2009-02-17]
OMIM:245800	Laurence-Moon syndrome		HP:0001249	PMID:25480986	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0001513	PMID:25480986	PCS		1/4			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-12-18]
OMIM:245800	Laurence-Moon syndrome		HP:0000533	PMID:25480986	PCS		3/4			P	HPO:probinson[2022-12-18]
OMIM:260470	Panencephalitis, subacute sclerosing		HP:0002383	OMIM:260470	IEA					P	HPO:skoehler[2009-02-17]
OMIM:260470	Panencephalitis, subacute sclerosing		HP:0000007	OMIM:260470	IEA					I	HPO:iea[2009-02-17]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0003202	PMID:19118816	PCS					P	HPO:probinson[2013-04-06]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0002483	PMID:19118816	PCS		6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-16]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0003474	PMID:19118816	PCS		0/9			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-16]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0003581	PMID:19118816	PCS		9/9			C	HPO:probinson[2022-06-16]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0002493	PMID:19118816	PCS					P	HPO:probinson[2013-04-06]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0007354	PMID:19118816	PCS		9/9			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-16]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0000762	PMID:19118816	PCS		0/9			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-16]
OMIM:612577	Amyotrophic lateral sclerosis 11		HP:0000006	PMID:19118816	PCS					I	HPO:probinson[2013-01-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000486	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0002540	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0004322	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0002783	PMID:22563157	PCS		2/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0001332	OMIM:208900	TAS					P	HPO:skoehler[2012-11-25]
OMIM:208900	Ataxia-telangiectasia		HP:0001250	PMID:22563157	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0001251	PMID:17628218	PCS		104/104			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000639	PMID:22563157	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0011463	PMID:22563157	PCS		2/2			C	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000957	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0001888	OMIM:208900	TAS					P	HPO:probinson[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0004315	OMIM:208900	IEA					P	HPO:iea[2012-05-06]
OMIM:208900	Ataxia-telangiectasia		HP:0000252	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000134	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0001266	PMID:17628218	PCS		81/93			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0001260	PMID:17628218	PCS		104/104			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0002110	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0002075	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0002073	PMID:22563157	PCS		2/2			P	HPO:probinson[2022-05-09];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0012539	OMIM:208900	TAS					P	HPO:skoehler[2014-01-28]
OMIM:208900	Ataxia-telangiectasia		HP:0012189	OMIM:208900	TAS					P	HPO:skoehler[2014-01-28]
OMIM:208900	Ataxia-telangiectasia		HP:0000524	PMID:22563157	PCS	HP:0011463	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000007	PMID:7792600	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000246	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0001337	OMIM:208900	TAS					P	HPO:skoehler[2012-11-25]
OMIM:208900	Ataxia-telangiectasia		HP:0002665	OMIM:208900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208900	Ataxia-telangiectasia		HP:0001336	OMIM:208900	TAS					P	HPO:skoehler[2012-11-25]
OMIM:208900	Ataxia-telangiectasia		HP:0002028	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0001595	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0005357	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0001350	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0002080	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000819	OMIM:208900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:208900	Ataxia-telangiectasia		HP:0001909	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0001508	PMID:17628218	PCS		39/104			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0000778	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0006254	PMID:22563157	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0002837	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0005403	OMIM:208900	TAS					P	HPO:probinson[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0000750	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0010975	PMID:22563157	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:208900	Ataxia-telangiectasia		HP:0000823	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0008348	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0006721	PMID:22563157	PCS		1/2			P	HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0001315	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0002720	PMID:22563157	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-09]
OMIM:208900	Ataxia-telangiectasia		HP:0001952	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:208900	Ataxia-telangiectasia		HP:0008669	OMIM:208900	IEA					P	HPO:iea[2009-02-17]
OMIM:142669	Hip dysplasia, Beukes type		HP:0001385	OMIM:142669	TAS					P	HPO:probinson[2009-02-17]
OMIM:142669	Hip dysplasia, Beukes type		HP:0005743	OMIM:142669	TAS					P	HPO:probinson[2013-04-07]
OMIM:142669	Hip dysplasia, Beukes type		HP:0006429	OMIM:142669	TAS					P	HPO:probinson[2009-02-17]
OMIM:142669	Hip dysplasia, Beukes type		HP:0011463	OMIM:142669	TAS					C	HPO:probinson[2012-07-28]
OMIM:142669	Hip dysplasia, Beukes type		HP:0008783	OMIM:142669	TAS					P	HPO:probinson[2009-02-17]
OMIM:142669	Hip dysplasia, Beukes type		HP:0003370	OMIM:142669	TAS					P	HPO:probinson[2015-02-28]
OMIM:142669	Hip dysplasia, Beukes type		HP:0005041	OMIM:142669	TAS					P	HPO:probinson[2015-02-28]
OMIM:142669	Hip dysplasia, Beukes type		HP:0003182	OMIM:142669	TAS					P	HPO:probinson[2009-02-17]
OMIM:142669	Hip dysplasia, Beukes type		HP:0002758	OMIM:142669	TAS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:142669	Hip dysplasia, Beukes type		HP:0000006	OMIM:142669	TAS					I	HPO:probinson[2009-02-17]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0002750	OMIM:229070	TAS					P	HPO:skoehler[2015-05-31]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0003199	OMIM:229070	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0011969	PMID:9280841;PMID:9271483	PCS		2/2			P	HPO:probinson[2022-03-20]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0011462	PMID:9280841	PCS		1/1			C	HPO:probinson[2022-03-20]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0030341	PMID:9280841;PMID:9271483	PCS		2/2			P	HPO:probinson[2022-03-20]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0000789	PMID:9280841	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-20]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0000007	PMID:8220432	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0004408	PMID:8220432	PCS		0/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2024-03-08]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0008734	OMIM:229070	TAS					P	HPO:skoehler[2015-05-31]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0000135	OMIM:229070	IEA					P	HPO:skoehler[2018-10-08]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0000786	PMID:9271483;PMID:8220432	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:229070	Hypogonadotropic hypogonadism 24 without anosmia		HP:0000027	OMIM:229070	IEA					P	HPO:skoehler[2018-10-08]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0000494	OMIM:106995	TAS					P	HPO:skoehler[2012-11-20]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0000430	OMIM:106995	TAS					P	HPO:skoehler[2012-11-16]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0002164	OMIM:106995	IEA					P	HPO:iea[2009-02-17]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0005793	OMIM:106995	IEA					P	HPO:iea[2009-02-17]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0000426	OMIM:106995	TAS					P	HPO:skoehler[2012-11-16]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0000448	OMIM:106995	TAS					P	HPO:skoehler[2012-11-16]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0009237	OMIM:106995	IEA					P	HPO:iea[2009-02-17]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0000218	OMIM:106995	TAS					P	HPO:skoehler[2012-11-16]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0008404	OMIM:106995	TAS					P	HPO:skoehler[2013-05-03]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0009943	OMIM:106995	IEA					P	HPO:iea[2009-02-17]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0000322	OMIM:106995	TAS					P	HPO:skoehler[2012-11-16]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0000006	OMIM:106995	IEA					I	HPO:iea[2009-02-17]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0001798	OMIM:106995	IEA					P	HPO:iea[2009-02-17]
OMIM:106995	Anonychia-Onychodystrophy with hypoplasia or absence of distal phalanges		HP:0006118	OMIM:106995	TAS					P	HPO:probinson[2012-06-11]
OMIM:611718	Hypomagnesemia 4, renal		HP:0002917	PMID:17671655	PCS		2/2			P	HPO:probinson[2013-04-01]
OMIM:611718	Hypomagnesemia 4, renal		HP:0001250	PMID:17671655	PCS		2/2			P	HPO:probinson[2013-04-01]
OMIM:611718	Hypomagnesemia 4, renal		HP:0001263	PMID:17671655	PCS		2/2			P	HPO:probinson[2013-04-01]
OMIM:611718	Hypomagnesemia 4, renal		HP:0000007	PMID:17671655	PCS					I	HPO:probinson[2013-01-09]
OMIM:108760	Atresia of external auditory canal and conduction deafness		HP:0005906	OMIM:108760	IEA					P	HPO:iea[2009-02-17]
OMIM:108760	Atresia of external auditory canal and conduction deafness		HP:0008773	OMIM:108760	IEA					P	HPO:iea[2009-02-17]
OMIM:108760	Atresia of external auditory canal and conduction deafness		HP:0000405	OMIM:108760	IEA					P	HPO:iea[2009-02-17]
OMIM:108760	Atresia of external auditory canal and conduction deafness		HP:0000006	OMIM:108760	IEA					I	HPO:iea[2009-02-17]
OMIM:108760	Atresia of external auditory canal and conduction deafness		HP:0000402	OMIM:108760	PCS					P	HPO:probinson[2012-03-31]
OMIM:108760	Atresia of external auditory canal and conduction deafness		HP:0000413	OMIM:108760	PCS					P	HPO:probinson[2012-03-31]
OMIM:614890	Immunodeficiency 29		HP:0020086	PMID:9854038	PCS	HP:0003593	1/1			P	HPO:probinson[2022-04-10]
OMIM:614890	Immunodeficiency 29		HP:0003593	PMID:9854038	PCS		1/1			C	HPO:probinson[2022-04-10]
OMIM:614890	Immunodeficiency 29		HP:0000007	PMID:9854038	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-10]
OMIM:614890	Immunodeficiency 29		HP:0002721	PMID:9854038	PCS					P	HPO:skoehler[2015-08-23];HPO:probinson[2022-04-10]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0002166	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0000012	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0003487	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0000020	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0002064	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0002061	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0011449	OMIM:607152	TAS					P	HPO:probinson[2012-04-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0011448	OMIM:607152	TAS					P	HPO:probinson[2012-04-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0007340	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0002839	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0001258	OMIM:607152	TAS					P	HPO:probinson[2012-04-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0000006	OMIM:607152	IEA					I	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0003677	OMIM:607152	IEA					C	HPO:iea[2009-02-17]
OMIM:607152	Spastic paraplegia 19, autosomal dominant		HP:0001347	OMIM:607152	IEA					P	HPO:iea[2009-02-17]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0003621	PMID:27432940	PCS		1/2			C	HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001332	PMID:27432940	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001395	PMID:27432940	PCS		2/2			P	HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001251	PMID:27432940	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0002040	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0031545	PMID:27432940	PCS		2/2			P	HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001409	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0011463	PMID:27432940	PCS		1/2			C	HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0033044	PMID:27432940	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0000938	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0000007	PMID:27432940	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0007763	PMID:27432940	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001511	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0002216	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0005528	PMID:27432940	PCS		2/2			P	HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0002239	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001510	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001257	PMID:27432940	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617341	Cerebroretinal microangiopathy with calcifications and cysts 2		HP:0001876	PMID:27432940	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:616739	Intellectual developmental disorder, autosomal recessive 51		HP:0000252	OMIM:616739	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616739	Intellectual developmental disorder, autosomal recessive 51		HP:0000750	PMID:26206890	PCS					P	HPO:probinson[2017-06-17]
OMIM:616739	Intellectual developmental disorder, autosomal recessive 51		HP:0001263	PMID:26206890	PCS					P	HPO:probinson[2017-06-17]
OMIM:616739	Intellectual developmental disorder, autosomal recessive 51		HP:0003593	OMIM:616739	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616739	Intellectual developmental disorder, autosomal recessive 51		HP:0000007	PMID:26206890	PCS					I	HPO:probinson[2017-06-17]
OMIM:616739	Intellectual developmental disorder, autosomal recessive 51		HP:0001270	OMIM:616739	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616739	Intellectual developmental disorder, autosomal recessive 51		HP:0001249	PMID:26206890	PCS					P	HPO:probinson[2017-06-17]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0003148	PMID:12579474	PCS		0/10			P	HPO:probinson[2013-12-15];HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0002684	OMIM:607634	IEA					P	HPO:iea[2009-02-17]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0005450	PMID:12579474	PCS		3/10			P	HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0000925	OMIM:607634	IEA					P	HPO:iea[2009-02-17]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0011002	PMID:12579474	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0000935	PMID:12579474	PCS		4/10			P	HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0100789	PMID:12579474	PCS		3/10			P	HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0200025	PMID:12579474	PCS		1/10			P	HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0002757	PMID:12579474	PCS		0/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0000405	OMIM:607634	IEA					P	HPO:iea[2009-02-17]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0002315	PMID:12579474	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0000006	PMID:12579474	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0002644	OMIM:607634	IEA					P	HPO:iea[2009-02-17]
OMIM:607634	Osteopetrosis, autosomal dominant 1		HP:0005789	OMIM:607634	IEA					P	HPO:iea[2009-02-17]
OMIM:240950	Hypogonadism-Cataract syndrome		HP:0000518	OMIM:240950	IEA					P	HPO:iea[2009-02-17]
OMIM:240950	Hypogonadism-Cataract syndrome		HP:0008232	OMIM:240950	TAS					P	HPO:iea[2012-07-18]
OMIM:240950	Hypogonadism-Cataract syndrome		HP:0000789	OMIM:240950	IEA					P	HPO:iea[2009-02-17]
OMIM:240950	Hypogonadism-Cataract syndrome		HP:0000007	OMIM:240950	IEA					I	HPO:iea[2009-02-17]
OMIM:240950	Hypogonadism-Cataract syndrome		HP:0000026	OMIM:240950	TAS					P	HPO:iea[2009-02-17]
OMIM:240950	Hypogonadism-Cataract syndrome		HP:0000135	OMIM:240950	IEA					P	HPO:skoehler[2010-06-18]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0001265	OMIM:613641	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0003376	OMIM:613641	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0033383	PMID:20920668	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0001761	OMIM:613641	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0001263	PMID:20920668	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0001284	OMIM:613641	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0009588	PMID:20920668	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0009027	OMIM:613641	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0000007	PMID:20920668	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0002936	OMIM:613641	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613641	Charcot-marie-tooth disease, recessive intermediate B		HP:0100716	PMID:20920668	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:237500	DUBIN-JOHNSON syndrome		HP:0002908	OMIM:237500	IEA					P	HPO:iea[2009-02-17]
OMIM:237500	DUBIN-JOHNSON syndrome		HP:0000007	OMIM:237500	IEA					I	HPO:iea[2009-02-17]
OMIM:237500	DUBIN-JOHNSON syndrome		HP:0001080	OMIM:237500	IEA					P	HPO:iea[2009-02-17]
OMIM:237500	DUBIN-JOHNSON syndrome		HP:0000952	OMIM:237500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0002025	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0002023	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000486	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000485	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0009918	PMID:8944018	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000482	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0003828	OMIM:180500	IEA					M	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000558	OMIM:180500	TAS					P	HPO:probinson[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000219	OMIM:180500	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000336	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000677	PMID:8944018	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000431	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000691	PMID:8944018	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0011500	OMIM:180500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000627	PMID:8944018	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-02]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000668	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000327	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0007873	OMIM:180500	TAS					P	HPO:probinson[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000824	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000526	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0007676	PMID:8944018	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000047	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000322	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000006	PMID:8944018	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:180500	Axenfeld-Rieger syndrome, type 1		HP:0000501	OMIM:180500	IEA					P	HPO:iea[2009-02-17]
OMIM:615224	Advanced sleep phase syndrome, familial, 2		HP:0006979	PMID:15800623	PCS					P	HPO:lccarmody[2018-09-19]
OMIM:615224	Advanced sleep phase syndrome, familial, 2		HP:0002076	OMIM:615224;PMID:23636092	PCS		20/20		HP:0011010	P	HPO:lccarmody[2018-09-19];HPO:lccarmody[2018-09-19];HP:probinson[2019-01-03];HPO:skoehler[2018-10-08]
OMIM:615224	Advanced sleep phase syndrome, familial, 2		HP:0002077	PMID:23636092	PCS					P	HPO:lccarmody[2018-09-19]
OMIM:615224	Advanced sleep phase syndrome, familial, 2		HP:0002083	PMID:23636092	PCS					P	HPO:lccarmody[2018-09-19]
OMIM:615224	Advanced sleep phase syndrome, familial, 2		HP:0031873	OMIM:615224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615224	Advanced sleep phase syndrome, familial, 2		HP:0000006	OMIM:615224	TAS					I	HPO:skoehler[2013-06-06]
OMIM:149700	Lacrimal duct defect		HP:0009926	PMID:24372406	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-07-15]
OMIM:149700	Lacrimal duct defect		HP:0030752	PMID:24372406	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-15]
OMIM:149700	Lacrimal duct defect		HP:0100539	OMIM:149700	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:149700	Lacrimal duct defect		HP:0000509	OMIM:149700	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:149700	Lacrimal duct defect		HP:0000007	PMID:24372406	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-07-15]
OMIM:149700	Lacrimal duct defect		HP:0000246	OMIM:149700	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:149700	Lacrimal duct defect		HP:0000620	OMIM:149700	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:149700	Lacrimal duct defect		HP:0000564	OMIM:149700	IEA					P	HPO:iea[2009-02-17]
OMIM:617433	Retinitis pigmentosa 78		HP:0000662	PMID:28132693	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:617433	Retinitis pigmentosa 78		HP:0030786	PMID:28132693	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:617433	Retinitis pigmentosa 78		HP:0001123	PMID:28132693	PCS		3/3			P	HPO:skoehler[2017-07-13]
OMIM:617433	Retinitis pigmentosa 78		HP:0011462	PMID:28132693	PCS		3/3			C	HPO:probinson[2023-06-10]
OMIM:617433	Retinitis pigmentosa 78		HP:0000007	PMID:28132693	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:617433	Retinitis pigmentosa 78		HP:0007663	PMID:28132693	PCS		3/3			P	HPO:skoehler[2017-07-13]
OMIM:617433	Retinitis pigmentosa 78		HP:0011505	PMID:28132693	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:617433	Retinitis pigmentosa 78		HP:0000543	PMID:28132693	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001650	PMID:9823488	PCS					P	HPO:probinson[2017-06-16]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001792	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001770	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001596	OMIM:100300	TAS					P	HPO:probinson[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001156	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001250	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001252	OMIM:100300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:100300	Adams-Oliver syndrome 1		HP:0030011	OMIM:100300	TAS					P	HPO:probinson[2017-06-16]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001290	OMIM:100300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:100300	Adams-Oliver syndrome 1		HP:0004383	PMID:9823488	PCS					P	HPO:probinson[2017-06-16]
OMIM:100300	Adams-Oliver syndrome 1		HP:0002084	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001629	OMIM:100300	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0002539	OMIM:100300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001647	PMID:9823488	PCS					P	HPO:probinson[2017-06-16]
OMIM:100300	Adams-Oliver syndrome 1		HP:0006970	OMIM:100300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:100300	Adams-Oliver syndrome 1		HP:0002119	OMIM:100300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:100300	Adams-Oliver syndrome 1		HP:0007589	OMIM:100300	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001302	OMIM:100300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001642	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0002558	OMIM:100300	TAS		20/20			P	HPO:probinson[2017-06-16];HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001249	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0004415	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000175	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000252	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001762	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0002079	OMIM:100300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001362	OMIM:100300	TAS	HP:0003577				P	HPO:probinson[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001263	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0002092	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:6000946	OMIM:100300	TAS					P	HPO:probinson[2024-08-04]
OMIM:100300	Adams-Oliver syndrome 1		HP:0007590	PMID:1424238	PCS					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000965	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000822	OMIM:100300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001636	PMID:9823488	PCS					P	HPO:probinson[2017-06-16]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000568	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000565	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0001631	OMIM:100300	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000204	OMIM:100300	IEA					P	HPO:iea[2009-02-17]
OMIM:100300	Adams-Oliver syndrome 1		HP:0002126	OMIM:100300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:100300	Adams-Oliver syndrome 1		HP:0000006	PMID:9823488	PCS					I	HPO:iea[2009-02-17]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0002069	PMID:15144424	PCS		46/60			P	HPO:probinson[2022-11-01];HPO:probinson[2024-03-10]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0002076	PMID:15144424	PCS		6/67			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-11-01];HPO:probinson[2024-03-10]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0002384	PMID:15144424	PCS		21/60			P	HPO:probinson[2022-11-01];HPO:probinson[2024-03-10]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0002373	PMID:15144424	PCS		2/60			P	HPO:probinson[2024-03-10]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0003829	PMID:15144424	PCS					I	HPO:skoehler[2012-11-25];HPO:probinson[2022-11-01]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0003593	PMID:15144424	PCS		67/67			C	HPO:probinson[2022-11-01];HPO:probinson[2024-03-10]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0012759	PMID:15144424	PCS		0/67			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-11-01];HPO:probinson[2024-03-10]
OMIM:605751	Seizures, benign familial infantile, 2		HP:0000006	PMID:22243967	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-01]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0003477	PMID:16333315	PCS					P	HPO:probinson[2012-03-12];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0001760	PMID:16333315	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0002169	PMID:16333315	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0003431	PMID:16333315	PCS					P	HPO:probinson[2012-03-12];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0003487	PMID:16333315	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0006827	PMID:16333315	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0003693	PMID:16333315	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0002064	PMID:16333315	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0002061	PMID:16333315	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0034075	PMID:16333315	PCS		2/2			P	HPO:probinson[2022-02-03]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0011463	PMID:16333315	PCS		4/4			C	HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0006121	PMID:16333315	PCS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0007078	PMID:16333315	PCS		4/4			P	HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0012153	PMID:16333315	PCS		2/2			P	HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0000007	PMID:16399879	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0002936	PMID:16333315	PCS					P	HPO:probinson[2012-03-12];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0003409	PMID:16333315	PCS		4/4			P	HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0001258	PMID:16333315	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0001347	PMID:16333315	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:256840	Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive		HP:0001886	PMID:16333315	PCS		1/4			P	HPO:probinson[2021-11-24]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0008715	PMID:21220346	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0003577	PMID:21220346	PCS		3/3			C	HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0000023	PMID:21220346	PCS		3/3			P	HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0000062	PMID:21220346	PCS		2/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0000051	PMID:21220346	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0002926	PMID:21220346	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0001636	PMID:21220346	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:4000094	PMID:21220346	PCS		1/3			P	HPO:probinson[2023-01-27]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0030260	PMID:21220346	PCS		1/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0000006	PMID:21220346	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-16]
OMIM:615542	Testicular anomalies with or without congenital heart disease		HP:0000028	PMID:21220346	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-16]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0001250	OMIM:300491	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0001419	OMIM:300491	TAS					I	HPO:skoehler[2009-02-17]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0000718	OMIM:300491	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0000729	OMIM:300491	TAS					P	HPO:skoehler[2013-05-31]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0001328	OMIM:300491	IEA					P	HPO:skoehler[2009-02-17]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0001423	OMIM:300491	TAS					I	HPO:skoehler[2013-05-29]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0000256	OMIM:300491	IEA		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:300491	Epilepsy, X-linked, with variable learning disabilities and behavior disorders		HP:0007359	OMIM:300491	TAS					P	HPO:probinson[2013-12-15]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000341	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0002421	PMID:28318499	PCS	HP:0003593	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0002069	PMID:28318499	PCS		1/1			P	HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0002089	PMID:28318499	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000486	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0001371	PMID:28318499	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0002384	PMID:28318499	PCS		1/1			P	HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0003273	PMID:28318499	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0003691	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0001252	PMID:28318499	PCS		1/1			P	HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0011461	PMID:28318499	PCS		9/9			C	HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0003826	PMID:28318499	PCS		2/9			C	HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000678	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0001989	PMID:28318499	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000218	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000411	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000278	PMID:28318499	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0006659	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0001762	PMID:28318499	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0005684	PMID:28318499	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0001284	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0012385	PMID:28318499	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0006380	PMID:28318499	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000508	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0002804	PMID:28318499	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000007	PMID:28318499	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0001558	PMID:28318499	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0006466	PMID:28318499	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000565	PMID:28318499	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0002987	PMID:28318499	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:617468	Arthrogryposis multiplex congenita, neurogenic, with myelin defect		HP:0000347	PMID:28318499	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0002013	PMID:29282386	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0002110	PMID:24726755	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0011947	PMID:24726755	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0000938	PMID:24726755	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0011473	PMID:29282386;PMID:24726755	PCS		2/2			P	HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0033994	PMID:30909251	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0000007	PMID:24726755	PCS					I	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0033996	PMID:30909251	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0003270	PMID:29282386	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0033995	PMID:30909251	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0005208	PMID:29282386;PMID:24726755	PCS		2/2			P	HPO:probinson[2021-08-21]
OMIM:619445	Diarrhea 12, with microvillus atrophy		HP:0001942	PMID:29282386;PMID:24726755	PCS		2/2			P	HPO:probinson[2021-08-21]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000365	PMID:22426308;PMID:23906836	PCS		1/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000684	PMID:22426308	PCS		2/2			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000486	PMID:23906836	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0004322	PMID:22426308	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001250	PMID:22426308;PMID:23906836	PCS		1/3			P	HPO:probinson[2022-07-02];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001252	PMID:22426308;PMID:23906836	PCS		3/4			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000280	PMID:22426308;PMID:23906836	PCS		4/4			P	HPO:probinson[2022-07-02];HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0012471	PMID:22426308	PCS		3/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000158	PMID:22426308;PMID:23906836	PCS		1/4			P	HPO:probinson[2022-07-02];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000752	PMID:23906836	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001249	PMID:23906836	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001007	PMID:22426308	PCS		3/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000252	PMID:22426308	PCS		1/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000175	PMID:22426308	PCS	HP:0003577	2/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000175	PMID:23906836	PCS		0/1			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000574	PMID:22426308;PMID:23906836	PCS		3/4			P	HPO:probinson[2022-07-02];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0002750	PMID:22426308;PMID:23906836	PCS		2/3			P	HPO:probinson[2022-07-02];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0011968	PMID:22426308	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0002033	PMID:22426308	PCS		3/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0200105	PMID:22426308	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001263	PMID:22426308	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000294	PMID:23906836	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0200104	PMID:22426308	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000527	PMID:22426308;PMID:23906836	PCS		4/4			P	HPO:probinson[2022-07-02];HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001852	PMID:23906836	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000322	PMID:22426308;PMID:23906836	PCS		2/4			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000006	PMID:22426308	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000445	PMID:22426308;PMID:23906836	PCS		3/4			P	HPO:probinson[2022-07-02];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001792	PMID:22426308;PMID:23906836	PCS		4/4			P	HPO:probinson[2022-07-02];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000343	PMID:22426308;PMID:23906836	PCS		1/4			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000463	PMID:23906836	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001156	OMIM:614607	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000023	PMID:22426308	PCS		1/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001273	OMIM:614607	TAS		3/3			P	HPO:probinson[2013-08-10]
OMIM:614607	Coffin-Siris syndrome 2		HP:0002719	PMID:22426308;PMID:23906836	PCS		3/4			P	HPO:probinson[2022-07-02];HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0009882	PMID:23906836	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001305	PMID:22426308	PCS	HP:0003577	1/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001627	PMID:23906836	PCS		0/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000218	PMID:22426308	PCS		2/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000377	PMID:23906836	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000179	PMID:23906836	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000154	PMID:22426308;PMID:23906836	PCS		4/4			P	HPO:probinson[2022-07-02];HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000750	PMID:23906836	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001321	PMID:22426308	PCS		1/2			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0005280	PMID:22426308;PMID:23906836	PCS		3/4			P	HPO:probinson[2022-07-02];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000508	PMID:23906836	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0002209	PMID:22426308	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000505	PMID:22426308	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0001511	PMID:22426308	PCS		1/3			P	HPO:probinson[2022-07-02]
OMIM:614607	Coffin-Siris syndrome 2		HP:0000028	PMID:23906836	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0008936	PMID:32623794	PCS		1/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0030215	PMID:32623794	PCS		1/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0005830	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0002376	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0001250	PMID:32623794	PCS		4/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0001272	PMID:32623794	PCS		1/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0002066	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0100490	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0030793	PMID:32623794	PCS		3/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0001350	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0000280	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0033720	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01];HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0011463	PMID:32623794	PCS		3/3			C	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0000748	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0011198	PMID:32623794	PCS		1/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0000007	PMID:32623794	PCS					I	HPO:probinson[2021-07-01];HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0002119	PMID:32623794	PCS		1/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0000648	PMID:32623794	PCS		2/4			P	HPO:probinson[2021-07-01]
OMIM:619323	Neurodevelopmental disorder with seizures and gingival overgrowth		HP:0000212	PMID:32623794	PCS		3/4			P	HPO:probinson[2021-07-01]
OMIM:606217	Atrioventricular septal defect, partial, with heterotaxy syndrome		HP:0003577	PMID:12632326	PCS		3/3			C	HPO:probinson[2022-09-02];HPO:probinson[2024-07-21]
OMIM:606217	Atrioventricular septal defect, partial, with heterotaxy syndrome		HP:0001651	PMID:12632326	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-21]
OMIM:606217	Atrioventricular septal defect, partial, with heterotaxy syndrome		HP:0003829	PMID:12632326	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-07-21]
OMIM:606217	Atrioventricular septal defect, partial, with heterotaxy syndrome		HP:0002627	PMID:12632326	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-21]
OMIM:606217	Atrioventricular septal defect, partial, with heterotaxy syndrome		HP:0011577	PMID:12632326	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:606217	Atrioventricular septal defect, partial, with heterotaxy syndrome		HP:0004935	PMID:12632326	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:606217	Atrioventricular septal defect, partial, with heterotaxy syndrome		HP:0000006	PMID:12632326	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-07-21]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000939	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000716	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000938	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0011462	PMID:16767104	PCS		3/4			C	HPO:probinson[2022-09-04]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000739	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000712	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000978	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000713	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000311	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0001268	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000138	PMID:16767104	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0003466	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0003621	PMID:16767104	PCS		1/4			C	HPO:probinson[2022-09-04]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0001580	PMID:16767104	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0001065	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000709	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0002808	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000822	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0001956	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0003118	OMIM:610475	IEA		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0002920	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000963	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0001579	OMIM:610475	IEA					P	HPO:iea[2009-02-17]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0000006	PMID:16767104	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:610475	Pigmented nodular adrenocortical disease, primary, 2		HP:0001733	PMID:16767104	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:600666	Polycystic kidney disease 3		HP:0003621	PMID:27259053	PCS		2/20			C	HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0001410	OMIM:600666	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:600666	Polycystic kidney disease 3		HP:0003596	PMID:27259053	PCS		14/20			C	HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0003584	PMID:27259053	PCS		2/20			C	HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0011462	PMID:27259053	PCS		2/20			C	HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0000822	PMID:27259053	PCS		6/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0001407	PMID:27259053	PCS		15/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0004944	PMID:27259053	PCS		2/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0000113	PMID:27259053	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:600666	Polycystic kidney disease 3		HP:0000006	PMID:27259053	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-21]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0003577	PMID:22464250	PCS		4/4			C	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000463	OMIM:614613	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0001156	PMID:22464250	PCS		4/4		HP:0012828	P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0002286	OMIM:614613	TAS					P	HPO:skoehler[2014-05-04]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0003196	PMID:22464250	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0010049	PMID:22464250	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0010743	PMID:22464250	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000819	OMIM:614613	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000717	OMIM:614613	TAS					P	HPO:skoehler[2014-05-04]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000635	OMIM:614613	TAS					P	HPO:skoehler[2014-05-04]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0002516	PMID:22464250	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000851	OMIM:614613	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000752	OMIM:614613	TAS					P	HPO:skoehler[2014-05-04]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000311	OMIM:614613	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0001249	PMID:22464250	PCS		4/4			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0009803	PMID:22464250	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0003502	OMIM:614613	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000750	PMID:22464250	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0004233	PMID:22464250	PCS					P	HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0002297	OMIM:614613	TAS					P	HPO:skoehler[2014-05-04]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0001263	OMIM:614613	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000272	OMIM:614613	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0011800	OMIM:614613	TAS					P	HPO:skoehler[2013-11-28]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0005280	PMID:22464250	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0010579	PMID:22464250	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0001511	PMID:22464250	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000047	OMIM:614613	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0003416	OMIM:614613	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000006	PMID:22464250	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000028	OMIM:614613	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0000303	PMID:22464250	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:614613	Acrodysostosis 2 with or without hormone resistance		HP:0001513	OMIM:614613	TAS					P	HPO:skoehler[2013-04-02]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0011462	PMID:18313022	PCS					C	HPO:probinson[2022-07-10]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0006682	PMID:18313022	PCS					P	HPO:probinson[2013-02-18]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0001635	OMIM:604400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0100749	OMIM:604400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0011663	PMID:18313022	PCS					P	HPO:probinson[2013-03-11]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0031972	OMIM:604400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0001962	OMIM:604400	TAS					P	HPO:skoehler[2013-06-06]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0006677	PMID:18313022	PCS					P	HPO:probinson[2013-02-18]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0000006	PMID:18313022	PCS					I	HPO:probinson[2013-01-09]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0004756	PMID:18313022	PCS					P	HPO:probinson[2013-02-18]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0001645	PMID:18313022	PCS					P	HPO:probinson[2013-02-18]
OMIM:604400	Arrhythmogenic right ventricular dysplasia, familial, 5		HP:0100660	OMIM:604400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:122850	Cranioacrofacial syndrome		HP:0000275	OMIM:122850	TAS					P	HPO:probinson[2013-04-08]
OMIM:122850	Cranioacrofacial syndrome		HP:0001629	OMIM:122850	IEA					P	HPO:iea[2009-02-17]
OMIM:122850	Cranioacrofacial syndrome		HP:0001642	OMIM:122850	IEA					P	HPO:iea[2009-02-17]
OMIM:122850	Cranioacrofacial syndrome		HP:0000006	OMIM:122850	IEA					I	HPO:iea[2009-02-17]
OMIM:122850	Cranioacrofacial syndrome		HP:0005922	OMIM:122850	TAS					P	HPO:probinson[2013-04-08]
OMIM:122850	Cranioacrofacial syndrome		HP:0005679	OMIM:122850	IEA					P	HPO:iea[2009-02-17]
OMIM:602071	Broad terminal phalanges, familial		HP:0010186	OMIM:602071	TAS					P	HPO:probinson[2012-06-09]
OMIM:602071	Broad terminal phalanges, familial		HP:0000006	OMIM:602071	TAS					I	HPO:probinson[2009-02-17]
OMIM:602071	Broad terminal phalanges, familial		HP:0009836	OMIM:602071	TAS					P	HPO:probinson[2012-06-09]
OMIM:614175	Meckel syndrome, type 10		HP:0000286	OMIM:614175	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614175	Meckel syndrome, type 10		HP:0002323	PMID:21763481	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0001250	OMIM:614175	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614175	Meckel syndrome, type 10		HP:0002085	PMID:21763481	PCS	HP:0011461	2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0009487	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0011461	PMID:31411728;PMID:21763481	PCS		3/3			C	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0002419	OMIM:614175	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614175	Meckel syndrome, type 10		HP:0001305	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0000377	OMIM:614175	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614175	Meckel syndrome, type 10		HP:0000054	PMID:31411728	PCS		1/1	MALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0000175	OMIM:614175	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614175	Meckel syndrome, type 10		HP:0001321	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0001162	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0002198	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0000193	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0045025	OMIM:614175	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614175	Meckel syndrome, type 10		HP:0100259	PMID:21763481	PCS	HP:0011461	2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0012385	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0000508	OMIM:614175	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614175	Meckel syndrome, type 10		HP:0000107	PMID:21763481	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0006563	PMID:21763481	PCS		2/2			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0000007	PMID:21763481	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0001830	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:614175	Meckel syndrome, type 10		HP:0002007	OMIM:614175	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614175	Meckel syndrome, type 10		HP:0000960	OMIM:614175	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614175	Meckel syndrome, type 10		HP:0000047	PMID:31411728	PCS		1/1	MALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-23]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0001377	PMID:16782820	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0011968	PMID:16782820	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0025278	PMID:16782820	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0004691	PMID:16782820	PCS		1/1			P	HPO:probinson[2013-04-12];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0030319	PMID:16782820	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0007141	PMID:16782820	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0002938	PMID:16782820	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0000007	PMID:16782820	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0002944	PMID:16782820	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0000218	PMID:16782820	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0002967	PMID:16782820	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0030084	PMID:16782820	PCS		1/1			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-10-24]
OMIM:610313	Cold-Induced sweating syndrome 2		HP:0000411	PMID:16782820	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:151100	Leopard syndrome 1		HP:0000286	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000242	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000486	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0001674	PMID:12058348	PCS		1/9			P	HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0004322	PMID:12058348	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000122	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0003298	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0003691	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0012569	OMIM:151100	TAS					P	HPO:probinson[2014-01-08]
OMIM:151100	Leopard syndrome 1		HP:0011710	OMIM:151100	TAS					P	HPO:probinson[2012-07-19]
OMIM:151100	Leopard syndrome 1		HP:0001709	OMIM:151100	TAS					P	HPO:probinson[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000957	PMID:12058348	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000316	PMID:12058348	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000411	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0001642	OMIM:151100	TAS		3/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000256	PMID:12058348	PCS		7/9			P	HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000457	OMIM:151100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:151100	Leopard syndrome 1		HP:0000358	PMID:12058348	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0002996	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0002751	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000175	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000054	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0001682	PMID:12058348	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0001003	PMID:12058348	PCS		9/9			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000470	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0010463	OMIM:151100	TAS					P	HPO:skoehler[2014-03-24]
OMIM:151100	Leopard syndrome 1		HP:0001639	PMID:12058348	PCS		3/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000407	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000508	PMID:12058348	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000921	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000767	PMID:12058348	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0004409	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0002967	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000823	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000768	PMID:12058348	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000047	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000465	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000006	PMID:12058348	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0000028	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000369	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000303	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0000325	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:151100	Leopard syndrome 1		HP:0001634	PMID:12058348	PCS		1/9			P	HPO:probinson[2023-02-20]
OMIM:151100	Leopard syndrome 1		HP:0008724	OMIM:151100	IEA					P	HPO:iea[2009-02-17]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0003577	PMID:33991472	PCS		5/8			C	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000343	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000365	PMID:33991472	PCS		3/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000023	PMID:33991472	PCS		5/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0004322	PMID:33991472	PCS		8/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0001156	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0003593	PMID:33991472	PCS		2/8			C	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000280	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0005272	PMID:33991472	PCS		6/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0010306	PMID:33991472	PCS		1/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0006191	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0002938	PMID:33991472	PCS		1/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0001328	PMID:33991472	PCS		3/7			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000218	PMID:33991472	PCS		5/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000455	PMID:33991472	PCS		8/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000179	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000973	PMID:33991472	PCS		8/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0003623	PMID:33991472	PCS		1/8			C	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0002553	PMID:33991472	PCS		6/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000494	PMID:33991472	PCS		5/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0001363	PMID:33991472	PCS		6/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000431	PMID:33991472	PCS		8/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0002650	PMID:33991472	PCS		2/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0002970	PMID:33991472	PCS		3/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0003300	PMID:33991472	PCS		1/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0001382	PMID:33991472	PCS		4/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0011968	PMID:33991472	PCS		3/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0034271	PMID:33991472	PCS		8/8			P	HPO:probinson[2022-09-05]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0034273	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-06-04]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0002827	PMID:33991472	PCS		1/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000767	PMID:33991472	PCS		1/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000007	PMID:33991472	PCS					I	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000527	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0004209	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000444	PMID:33991472	PCS		7/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0001159	PMID:33991472	PCS		5/8			P	HPO:probinson[2022-04-27]
OMIM:619451	Cutis laxa, autosomal recessive, type IIE		HP:0000520	PMID:33991472	PCS		6/8			P	HPO:probinson[2022-04-27]
OMIM:618767	Meesmann corneal dystrophy 2		HP:0000495	PMID:26788030	PCS					P	HPO:probinson[2020-04-29]
OMIM:618767	Meesmann corneal dystrophy 2		HP:0009926	PMID:26788030	PCS					P	HPO:probinson[2020-04-29]
OMIM:618767	Meesmann corneal dystrophy 2		HP:0000613	PMID:26788030	PCS					P	HPO:probinson[2020-04-29]
OMIM:618767	Meesmann corneal dystrophy 2		HP:0000006	PMID:26788030	PCS					I	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:106070	Angioma, hereditary neurocutaneousspinal arterial venous malformations with cutaneous hemangiomas, included		HP:0002277	OMIM:106070	IEA					P	HPO:iea[2009-02-17]
OMIM:106070	Angioma, hereditary neurocutaneousspinal arterial venous malformations with cutaneous hemangiomas, included		HP:0000790	OMIM:106070	IEA					P	HPO:skoehler[2010-06-20]
OMIM:106070	Angioma, hereditary neurocutaneousspinal arterial venous malformations with cutaneous hemangiomas, included		HP:0001269	OMIM:106070	IEA					P	HPO:iea[2009-02-17]
OMIM:106070	Angioma, hereditary neurocutaneousspinal arterial venous malformations with cutaneous hemangiomas, included		HP:0002239	OMIM:106070	IEA					P	HPO:iea[2009-02-17]
OMIM:106070	Angioma, hereditary neurocutaneousspinal arterial venous malformations with cutaneous hemangiomas, included		HP:0000006	OMIM:106070	IEA					I	HPO:iea[2009-02-17]
OMIM:106070	Angioma, hereditary neurocutaneousspinal arterial venous malformations with cutaneous hemangiomas, included		HP:0001028	OMIM:106070	IEA					P	HPO:skoehler[2010-06-20]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000200	PMID:29138412	PCS		1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000343	PMID:29138412	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0005257	PMID:29138412	PCS		4/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0001156	PMID:29138412	PCS		4/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0001371	PMID:29138412	PCS		2/3			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0001252	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0005792	PMID:29138412	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0012506	PMID:29138412	PCS		2/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0012368	PMID:29138412	PCS		3/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0034044	PMID:31816441;PMID:29138412	PCS		2/5			P	HPO:probinson[2022-02-03]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0011461	PMID:29138412	PCS		1/4			C	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0008873	PMID:29138412;PMID:31816441	PCS		5/5			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000998	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0002419	PMID:29138412;PMID:31816441	PCS		2/5			P	HPO:probinson[2021-10-09];HPO:probinson[2021-10-09];HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0002119	PMID:29138412	PCS		1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000774	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000358	PMID:29138412	PCS		1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0003865	PMID:29138412	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0003026	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0006956	PMID:29138412	PCS		2/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000054	PMID:29138412	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000750	PMID:29138412	PCS		3/3			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000431	PMID:29138412	PCS		1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0002079	PMID:29138412	PCS		2/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0011968	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0002195	PMID:29138412	PCS		3/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000691	PMID:29138412	PCS		2/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0002194	PMID:29138412	PCS		3/3			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0033454	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0005280	PMID:29138412	PCS		2/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000007	PMID:29138412	PCS					I	HPO:probinson[2021-10-09];HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0001538	PMID:29138412	PCS		3/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0002007	PMID:29138412	PCS		3/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000047	PMID:29138412	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000369	PMID:29138412	PCS		2/4			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0002643	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:619479	Short-rib thoracic dysplasia 21 without polydactyly		HP:0000687	PMID:31816441	PCS		1/1			P	HPO:probinson[2021-10-09]
OMIM:192605	Ventricular tachycardia, familial		HP:0004751	PMID:9637720	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-04]
OMIM:192605	Ventricular tachycardia, familial		HP:0001442	PMID:9637720	PCS					I	HPO:probinson[2022-10-04]
OMIM:192605	Ventricular tachycardia, familial		HP:0003581	PMID:9637720	PCS		1/1			C	HPO:probinson[2022-10-04]
OMIM:192605	Ventricular tachycardia, familial		HP:0011712	OMIM:192605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:192605	Ventricular tachycardia, familial		HP:0001638	PMID:9637720	PCS		0/1			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-10-04]
OMIM:192605	Ventricular tachycardia, familial		HP:0000006	PMID:9637720	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-04]
OMIM:192605	Ventricular tachycardia, familial		HP:0001645	OMIM:192605	IEA					P	HPO:iea[2009-02-17]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0002014	PMID:29751004	PCS		3/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0025452	PMID:29751004	PCS		2/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0002110	PMID:29751004	PCS		3/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0010976	PMID:29751004	PCS		6/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0011107	PMID:29751004	PCS		4/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0009098	PMID:29751004	PCS		1/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0002719	PMID:29751004	PCS		6/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0031394	PMID:29751004	PCS		2/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0001328	PMID:29751004	PCS					P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0001954	PMID:29751004	PCS		2/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0000007	PMID:29751004	PCS					I	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0002716	PMID:29751004	PCS		2/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0006532	PMID:29751004	PCS		4/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0001744	PMID:29751004	PCS		1/6			P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0001875	OMIM:150550	TAS					P	HPO:skoehler[2010-06-20]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0025615	PMID:29751004	PCS					P	HPO:probinson[2020-08-26]
OMIM:150550	Periodic fever, immunodeficiency, and thrombocytopenia syndrome		HP:0004854	PMID:29751004	PCS		2/6			P	HPO:probinson[2020-08-26]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0003577	PMID:17436019	PCS		2/2			C	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0003236	PMID:17436019	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0001371	OMIM:613154	TAS					P	HPO:skoehler[2013-05-31]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0006829	OMIM:613154	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0000580	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0001290	PMID:17436019	PCS		2/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0100297	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0007082	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0012110	OMIM:613154	TAS					P	HPO:skoehler[2014-09-21]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0007260	OMIM:613154	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0007063	PMID:17436019	PCS		2/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0011484	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0000519	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0001305	PMID:17436019	PCS		1/2			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0000238	PMID:17436019	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0002119	OMIM:613154	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0025435	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0001249	OMIM:613154	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0031956	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0006956	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0001321	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0001263	PMID:17436019	PCS		2/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0001284	PMID:17436019	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0003560	PMID:17436019	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0008081	PMID:17436019	PCS		1/2			P	HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0000007	PMID:17436019	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0000648	PMID:17436019	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:613154	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6		HP:0007973	PMID:17436019	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:231670	Glutaric acidemia I		HP:0001298	PMID:32777384	PCS		32/53			P	HPO:probinson[2022-10-13]
OMIM:231670	Glutaricaciduria, type I		HP:0006846	PMID:27672653	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaricaciduria, type I		HP:0002540	PMID:27672653	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0003530	OMIM:231670	IEA					P	HPO:skoehler[2015-01-27]
OMIM:231670	Glutaric acidemia I		HP:0001332	PMID:27672653;OMIM:231670	PCS		41/60			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0001250	PMID:32777384;PMID:27672653	PCS		21/60			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:skoehler[2012-11-18];HPO:probinson[2022-10-13]
OMIM:231670	Glutaric acidemia I		HP:0002063	OMIM:231670	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231670	Glutaric acidemia I		HP:0001252	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0003593	PMID:32777384;PMID:27672653	PCS		44/59			C	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2022-10-13]
OMIM:231670	Glutaric acidemia I		HP:0410175	OMIM:231670	IEA					P	HPO:skoehler[2018-10-08]
OMIM:231670	Glutaric acidemia I		HP:0002240	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0003150	PMID:32777384;PMID:27672653	PCS		54/60			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0001290	OMIM:231670	TAS					P	HPO:skoehler[2017-07-13]
OMIM:231670	Glutaricaciduria, type I		HP:0034656	PMID:27672653	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0002919	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0001508	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaricaciduria, type I		HP:0000737	PMID:27672653	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0011463	PMID:32777384	PCS		11/52			C	HPO:probinson[2022-10-13]
OMIM:231670	Glutaric acidemia I		HP:0001943	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0000238	PMID:32777384;PMID:27672653	PCS		9/59			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2022-10-13]
OMIM:231670	Glutaricaciduria, type I		HP:0100309	PMID:27672653	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0001946	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0006873	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0007105	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0000256	PMID:32777384;PMID:27672653	PCS		40/60			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-13];ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0001942	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0003623	PMID:32777384	PCS		1/52			C	HPO:probinson[2022-10-13]
OMIM:231670	Glutaric acidemia I		HP:0002179	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0001264	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0006956	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0003621	PMID:32777384	PCS		3/52			C	HPO:probinson[2022-10-13]
OMIM:231670	Glutaricaciduria, type I		HP:0002059	PMID:27672653	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0000750	PMID:32777384	PCS		15/52			P	HPO:probinson[2022-10-13]
OMIM:231670	Glutaricaciduria, type I		HP:0001344	PMID:27672653	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaricaciduria, type I		HP:0002376	PMID:27672653	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0001266	OMIM:231670	IEA					P	HPO:iea[2009-02-17]
OMIM:231670	Glutaric acidemia I		HP:0001263	PMID:32777384	PCS					P	HPO:probinson[2022-10-13];HPO:probinson[2022-10-13]
OMIM:231670	Glutaric acidemia I		HP:0034688	PMID:16641220	PCS		181/181			P	HPO:probinson[2023-03-31]
OMIM:231670	Glutaricaciduria, type I		HP:0100952	PMID:27672653	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaricaciduria, type I		HP:0033442	PMID:27672653	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:231670	Glutaric acidemia I		HP:0000007	OMIM:231670	IEA					I	HPO:iea[2009-02-17]
OMIM:601544	Deafness, autosomal dominant nonsyndromic sensorineural 3		HP:0000407	OMIM:601544	TAS					P	HPO:skoehler[2010-06-18]
OMIM:601544	Deafness, autosomal dominant nonsyndromic sensorineural 3		HP:0000006	OMIM:601544	TAS					I	HPO:skoehler[2009-02-17]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0002223	OMIM:263650	IEA					P	HPO:iea[2009-02-17]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000561	OMIM:263650	IEA					P	HPO:iea[2009-02-17]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0002025	PMID:22197489	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0007759	PMID:22197488	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000882	OMIM:263650	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0002023	PMID:28940926	PCS		1/1			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001371	PMID:22197489	PCS		3/3			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0010609	PMID:22197488	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000086	PMID:22197489	PCS		1/3			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0003031	PMID:22197489	PCS		1/2			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000042	PMID:28940926	PCS		1/1			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0003196	PMID:28940926	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0010489	PMID:22197489	PCS		3/3			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0010049	PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000958	PMID:22197489	PCS		3/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0011461	PMID:28940926	IEA		1/1			C	HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000316	PMID:22197488	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0032527	PMID:22197489	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000175	PMID:22197489	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000054	PMID:22197489	PCS		1/1			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000298	PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000050	PMID:22197488	PCS		1/1	MALE		P	HPO:skoehler[2012-11-18];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001060	PMID:22197489	PCS		2/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0010285	PMID:22197488;PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000327	OMIM:263650	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000568	OMIM:263650	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000007	PMID:22197488	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0009777	PMID:22197488	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001539	PMID:28940926	PCS		1/1			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0008689	OMIM:263650	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0002866	PMID:22197489	PCS		2/3			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0009778	PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001059	PMID:28940926	PCS		1/1			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000204	PMID:22197489	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000369	PMID:22197489	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001655	PMID:22197489	PCS		1/3			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0007418	PMID:22197488	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0003577	PMID:22197489	PCS		4/4			C	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001792	PMID:22197489	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000582	PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001596	PMID:22197489	IEA		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000023	PMID:22197489	PCS		1/3			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000062	OMIM:263650	TAS					P	HPO:skoehler[2012-10-17]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0012804	PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000581	PMID:22197489	PCS		3/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0008551	PMID:28940926	PCS		1/1			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000656	PMID:22197489	PCS		3/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000813	PMID:22197489	PCS		1/1			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000378	OMIM:263650	TAS		HP:0040283			P	HPO:skoehler[2013-05-31]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000059	PMID:22197489	PCS		3/3	FEMALE		P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0006610	PMID:22197489	PCS		3/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000652	PMID:22197489	PCS		2/3			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0009803	OMIM:263650	IEA					P	HPO:iea[2009-02-17]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0009826	PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001762	PMID:28940926;PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0030004	PMID:22197489	PCS		1/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000430	PMID:22197489	PCS		4/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000470	PMID:22197489	PCS		3/4			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0011224	PMID:28940926	PCS		1/1			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0012165	PMID:22197488	PCS		1/1			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0002209	PMID:22197488	PCS		1/1			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0002804	PMID:28940926;PMID:22197489	PCS		3/3			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001558	PMID:28940926	PCS		1/1			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0009755	PMID:22197488;PMID:22197489	PCS		4/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001511	OMIM:263650	TAS					P	HPO:skoehler[2012-10-17]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001159	PMID:28940926;PMID:22197489	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-19];HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0009756	PMID:22197488;PMID:22197489	PCS		5/5			P	HPO:probinson[2021-06-19];HPO:skoehler[2010-06-20];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0003974	PMID:22197489	PCS		1/2			P	HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0000347	PMID:22197489	PCS		3/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-06-19]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0001798	OMIM:263650	IEA					P	HPO:iea[2009-02-17]
OMIM:263650	Popliteal pterygium syndrome, Bartsocas-Papas type 1		HP:0002006	PMID:28940926;OMIM:263650	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:616038	Neu-Laxova syndrome 2		HP:0003577	PMID:25152457	PCS		12/12			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000340	PMID:25152457	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001770	PMID:25152457	PCS		7/12			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000518	PMID:25152457	PCS		2/7			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000316	PMID:25152457	PCS		9/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0002119	PMID:25152457	PCS		2/5			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000218	PMID:25152457	PCS		3/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0002414	PMID:25152457	PCS		1/11			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0006610	PMID:25152457	PCS		3/7			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000457	PMID:25152457	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000175	PMID:25152457	PCS		3/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000252	PMID:25152457	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001561	PMID:25152457	PCS		3/8			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0002650	PMID:25152457	PCS		3/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001321	PMID:25152457	PCS		3/6			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000470	PMID:25152457	PCS		11/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0011224	PMID:25152457	PCS		9/12			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0008064	PMID:25152457	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001838	PMID:25152457	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000969	PMID:25152457	PCS		8/11			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001339	PMID:25152457	PCS		3/7			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000007	PMID:25152457	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001558	PMID:25152457	PCS		7/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0006101	PMID:25152457	PCS		3/12			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001538	PMID:25152457	PCS		1/12			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0001511	PMID:25152457	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000520	PMID:25152457	PCS		9/12			P	HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000369	PMID:25152457	PCS		11/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:616038	Neu-Laxova syndrome 2		HP:0000347	PMID:25152457	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003378	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003431	PMID:17060578	PCS		1/1		HP:0012825	P	HPO:probinson[2012-03-12];HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003376	PMID:17060578	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003693	OMIM:600882	TAS					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003474	OMIM:600882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0002460	OMIM:600882	TAS					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0002380	PMID:17060578	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0007141	PMID:17060578	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0009027	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001868	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001763	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001886	PMID:17060578	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001765	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001265	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003621	PMID:17060578	PCS		1/1			C	HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001761	PMID:17060578	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0006937	PMID:17060578	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001284	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003384	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003380	OMIM:600882	PCS				HP:0012825	P	HPO:probinson[2012-03-12]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0033383	PMID:17060578	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0009053	PMID:17060578	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001218	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0009830	OMIM:600882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0000763	OMIM:600882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0003438	PMID:17060578	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0000006	PMID:12545426	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-24]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0001810	OMIM:600882	IEA					P	HPO:probinson[2009-02-17]
OMIM:600882	Charcot-Marie-Tooth disease, axonal, type 2B		HP:0008944	PMID:17060578	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:618015	Protoporphyria, erythropoietic, 2		HP:0012187	PMID:28874591	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:618015	Protoporphyria, erythropoietic, 2		HP:0001891	PMID:28874591	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:618015	Protoporphyria, erythropoietic, 2		HP:0000992	PMID:28874591	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:618015	Protoporphyria, erythropoietic, 2		HP:0003593	PMID:28874591	PCS		1/1			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:618015	Protoporphyria, erythropoietic, 2		HP:0000006	PMID:28874591	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-02-10]
OMIM:618773	Lymphatic malformation 8		HP:0001561	PMID:30115739	PCS	HP:0011461	2/2			P	HPO:probinson[2020-05-09]
OMIM:618773	Lymphatic malformation 8		HP:0002202	PMID:30115739	PCS	HP:0011461				P	HPO:probinson[2020-05-09]
OMIM:618773	Lymphatic malformation 8		HP:0001790	PMID:30115739	PCS	HP:0011461	2/2			P	HPO:probinson[2020-05-09]
OMIM:618773	Lymphatic malformation 8		HP:0007430	PMID:30115739	PCS					P	HPO:probinson[2020-05-09]
OMIM:618773	Lymphatic malformation 8		HP:0003826	PMID:30115739	PCS					C	HPO:probinson[2020-05-09]
OMIM:618773	Lymphatic malformation 8		HP:0000007	PMID:30115739	PCS					I	HPO:probinson[2020-05-09];HPO:probinson[2020-05-09]
OMIM:618773	Lymphatic malformation 8		HP:0001698	PMID:30115739	PCS	HP:0011461				P	HPO:probinson[2020-05-09]
OMIM:611031	Episodic kinesigenic dyskinesia 2		HP:0001332	OMIM:611031	TAS					P	HPO:probinson[2009-02-17]
OMIM:611031	Episodic kinesigenic dyskinesia 2		HP:0007166	OMIM:611031	TAS					P	HPO:probinson[2013-03-30]
OMIM:611031	Episodic kinesigenic dyskinesia 2		HP:0002072	OMIM:611031	IEA					P	HPO:iea[2009-02-17]
OMIM:611031	Episodic kinesigenic dyskinesia 2		HP:0000006	OMIM:611031	IEA					I	HPO:iea[2009-02-17]
OMIM:611031	Episodic kinesigenic dyskinesia 2		HP:0004305	OMIM:611031	TAS					P	HPO:probinson[2013-03-30]
OMIM:611031	Episodic kinesigenic dyskinesia 2		HP:0100660	OMIM:611031	TAS				HP:0025303	P	HPO:skoehler[2013-06-06]
OMIM:235370	Hemolytic anemia with thermal sensitivity of red cells		HP:0000007	OMIM:235370	IEA					I	HPO:iea[2009-02-17]
OMIM:235370	Hemolytic anemia with thermal sensitivity of red cells		HP:0004804	OMIM:235370	IEA					P	HPO:iea[2009-02-17]
OMIM:614149	Nail disorder, nonsyndromic congenital, 9		HP:0008400	OMIM:614149	TAS					P	HPO:skoehler[2013-06-03]
OMIM:614149	Nail disorder, nonsyndromic congenital, 9		HP:0000007	OMIM:614149	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614149	Nail disorder, nonsyndromic congenital, 9		HP:0001802	OMIM:614149	TAS					P	HPO:skoehler[2013-06-03]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0003236	PMID:32413282	PCS		11/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0001283	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0002460	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0012548	PMID:32413282	PCS		7/7			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0030319	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0100297	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0011462	PMID:32413282	PCS					C	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0000508	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0003805	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0000006	PMID:32413282	PCS					I	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0000544	PMID:32413282	PCS		11/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0003458	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14]
OMIM:618940	Oculopharyngodistal myopathy 2		HP:0003557	PMID:32413282	PCS		12/12			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0002135	PMID:33230297	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0002059	PMID:33230297	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0003577	PMID:33230297	PCS		2/2			C	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0000639	PMID:33230297	PCS		1/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0001250	PMID:33230297	PCS		1/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0000737	PMID:33230297	PCS	HP:0003623	2/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0000050	PMID:33230297	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0000007	PMID:33230297	PCS					I	HPO:probinson[2021-10-17];HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0012229	PMID:33230297	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0011344	PMID:33230297	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:619486	Aicardi-Goutieres syndrome 8		HP:0002500	PMID:33230297	PCS		2/2			P	HPO:probinson[2021-10-17]
OMIM:618798	Beck-Fahrner syndrome		HP:0000486	PMID:31928709	PCS		1/10			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000343	PMID:31928709	PCS		4/9			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001250	PMID:31928709	PCS		4/12			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001290	PMID:31928709	PCS		9/12			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0010862	PMID:31928709	PCS		9/10			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000716	PMID:31928709	PCS		1/6			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000639	PMID:31928709	PCS		2/10			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001629	PMID:31928709	PCS		1/7			P	HPO:probinson[2020-05-18];HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000739	PMID:31928709	PCS		3/6			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0006970	PMID:31928709	PCS		1/8			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0008872	PMID:31928709	PCS		4/7			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000337	PMID:31928709	PCS					P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0002119	PMID:31928709	PCS		1/8		HP:0012825	P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000218	PMID:31928709	PCS		3/8			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000411	PMID:31928709	PCS		4/8			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000256	PMID:31928709	PCS	HP:0003593	2/11			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001763	PMID:31928709	PCS		1/7			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001249	PMID:31928709	PCS		6/7			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000297	PMID:31928709	PCS		4/8			P	HPO:probinson[2020-05-18];HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000252	PMID:31928709	PCS		1/11			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001385	PMID:31928709	PCS		1/7			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000750	PMID:31928709	PCS		9/9			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0002353	PMID:31928709	PCS		4/8			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001640	PMID:31928709	PCS		1/7			P	HPO:probinson[2020-05-18];HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000276	PMID:31928709	PCS		5/10			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001382	PMID:31928709	PCS		1/7			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000194	PMID:31928709	PCS		4/8			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0001263	PMID:31928709	PCS		11/11			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0002194	PMID:31928709	PCS		10/10			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0012510	PMID:31928709	PCS		2/8			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0012760	PMID:31928709	PCS		6/6			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000729	PMID:31928709	PCS		5/6			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000508	PMID:31928709	PCS		1/10			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000007	PMID:31928709	PCS					I	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000348	PMID:31928709	PCS					P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0005616	PMID:31928709	PCS		1/7			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0007018	PMID:31928709	PCS		3/6			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0007678	PMID:31928709	PCS		1/10			P	HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000006	PMID:31928709	PCS					I	HPO:probinson[2020-05-18];HPO:probinson[2020-05-18]
OMIM:618798	Beck-Fahrner syndrome		HP:0000248	PMID:31928709	PCS		4/8			P	HPO:probinson[2020-05-18]
OMIM:252300	Morquio syndrome C		HP:0003510	OMIM:252300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252300	Morquio syndrome C		HP:0003610	OMIM:252300	IEA					P	HPO:iea[2009-02-17]
OMIM:252300	Morquio syndrome C		HP:0007957	OMIM:252300	IEA					P	HPO:iea[2009-02-17]
OMIM:252300	Morquio syndrome C		HP:0000926	OMIM:252300	IEA					P	HPO:iea[2009-02-17]
OMIM:252300	Morquio syndrome C		HP:0000007	OMIM:252300	IEA					I	HPO:iea[2009-02-17]
OMIM:252300	Morquio syndrome C		HP:0001249	OMIM:252300	IEA					P	HPO:iea[2009-02-17]
OMIM:252300	Morquio syndrome C		HP:0002655	OMIM:252300	IEA					P	HPO:iea[2009-02-17]
OMIM:252300	Morquio syndrome C		HP:0005723	OMIM:252300	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000365	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000486	PMID:18799783	PCS		0/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001272	PMID:18799783	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001250	PMID:18799783	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001252	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0003196	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001251	PMID:18799783	PCS		4/6			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001290	OMIM:256600	TAS					P	HPO:skoehler[2017-07-13]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002062	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002180	OMIM:256600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000639	PMID:18799783	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0011463	PMID:18799783	PCS		6/6			C	HPO:probinson[2022-04-04];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0011220	OMIM:256600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002317	OMIM:256600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001249	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001347	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0003444	PMID:18799783	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000572	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002059	PMID:18799783	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0003324	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002510	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000750	PMID:18799783	PCS		3/6			P	HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002376	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001263	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0001284	OMIM:256600	IEA					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002171	PMID:18799783	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0012675	PMID:16783378;PMID:18799783	PCS		7/7			P	HPO:probinson[2022-04-04];HPO:probinson[2022-04-04];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0012760	PMID:18799783	PCS		2/6			P	HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000649	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0007256	OMIM:256600	TAS					P	HPO:skoehler[2015-01-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000007	PMID:16783378	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002529	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000648	PMID:18799783	PCS	HP:0011463	4/6			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0002007	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000762	PMID:18799783	PCS		5/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-04-04]
OMIM:256600	Neurodegeneration with brain iron accumulation 2A		HP:0000347	OMIM:256600	IEA					P	HPO:iea[2009-02-17]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0002014	PMID:11479731	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-26];HPO:probinson[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0001298	PMID:33045405	PCS		9/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0001397	PMID:33045405	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0031956	PMID:11479731	PCS		1/1			P	HPO:probinson[2023-01-26]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0003621	PMID:33045405	PCS		1/29			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0002013	PMID:11479731	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-26];HPO:probinson[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0001250	PMID:33045405	PCS		13/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0002240	PMID:33045405	PCS		15/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-26];HPO:probinson[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0030781	PMID:33045405	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0003593	PMID:33045405	PCS		15/29			C	HPO:probinson[2023-01-26];HPO:probinson[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0002570	PMID:33045405	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0031964	PMID:11479731	PCS		1/1			P	HPO:probinson[2023-01-26]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0002919	PMID:33045405	PCS		7/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0011463	PMID:33045405	PCS		13/29			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0040155	PMID:33045405	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0000007	PMID:11228257	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-26]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0001943	PMID:33045405	PCS		25/28			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0025435	PMID:11479731	PCS		1/1			P	HPO:probinson[2023-01-26]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0002910	PMID:33045405	PCS		13/16			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0003215	PMID:33045405	PCS		21/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0002148	PMID:33045405	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0001942	PMID:33045405	PCS		20/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0001259	PMID:33045405	PCS		16/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605911	HMG-CoA synthase-2 deficiency		HP:0001325	PMID:11479731	PCS		1/1			P	HPO:probinson[2023-01-26]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0003202	PMID:22801503	PCS					P	HPO:probinson[2013-08-10]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0002015	PMID:22801503	PCS					P	HPO:probinson[2013-08-10]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0001260	PMID:22801503	PCS					P	HPO:probinson[2013-08-10]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0002380	PMID:22801503	PCS					P	HPO:probinson[2013-08-10]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0007354	PMID:22801503	PCS					P	HPO:probinson[2013-08-10]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0001324	PMID:22801503	PCS					P	HPO:probinson[2013-08-10]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0001257	PMID:22801503	PCS					P	HPO:probinson[2013-08-10]
OMIM:614808	Amyotrophic lateral sclerosis 18		HP:0000006	PMID:22801503	PCS					I	HPO:probinson[2013-08-10]
OMIM:165500	Optic atrophy 1		HP:0003587	OMIM:165500	IEA					C	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000552	OMIM:165500	IEA					P	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000486	OMIM:165500	PCS		10%			P	HPO:probinson[2012-04-01]
OMIM:165500	Optic atrophy 1		HP:0000650	OMIM:165500	IEA					P	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000980	OMIM:165500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:165500	Optic atrophy 1		HP:0000590	PMID:20157015	PCS		48/104			P	HPO:probinson[2012-04-01]
OMIM:165500	Optic atrophy 1		HP:0001251	PMID:20157015	PCS		31/104			P	HPO:probinson[2012-04-01]
OMIM:165500	Optic atrophy 1		HP:0003829	OMIM:165500	IEA					I	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0007663	OMIM:165500	TAS					P	HPO:skoehler[2015-07-26]
OMIM:165500	Optic atrophy 1		HP:0000505	OMIM:165500	IEA					P	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000648	OMIM:165500	IEA					P	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000603	OMIM:165500	IEA					P	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000576	OMIM:165500	IEA					P	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000642	OMIM:165500	IEA					P	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0003701	PMID:20157015	PCS		37/104			P	HPO:probinson[2012-04-01]
OMIM:165500	Optic atrophy 1		HP:0000006	OMIM:165500	IEA					I	HPO:iea[2009-02-17]
OMIM:165500	Optic atrophy 1		HP:0000666	OMIM:165500	PCS		5%			P	HPO:probinson[2012-04-01]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000670	OMIM:161000	IEA					P	HPO:iea[2009-02-17]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0001808	OMIM:161000	IEA					P	HPO:iea[2009-02-17]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0006480	OMIM:161000	IEA					P	HPO:iea[2009-02-17]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0002046	OMIM:161000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0007455	PMID:16960809	PCS					P	HPO:probinson[2022-09-25]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000966	PMID:16960809	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0007588	PMID:16960809	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000982	PMID:16960809	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:161000	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000006	PMID:16960809	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:619492	Cardiomyopathy, dilated, 2E		HP:0003819	PMID:31227780	PCS		2/4			C	HPO:probinson[2021-09-13]
OMIM:619492	Cardiomyopathy, dilated, 2E		HP:0000007	PMID:30384889	PCS					I	HPO:probinson[2021-09-13];HPO:probinson[2021-09-13]
OMIM:619492	Cardiomyopathy, dilated, 2E		HP:0006673	PMID:31227780	PCS	HP:0003593	1/1			P	HPO:probinson[2021-09-13]
OMIM:619492	Cardiomyopathy, dilated, 2E		HP:0001522	PMID:31227780	PCS		2/4			C	HPO:probinson[2021-09-13]
OMIM:619492	Cardiomyopathy, dilated, 2E		HP:0010316	PMID:31227780	PCS	HP:0003577	1/4			P	HPO:probinson[2021-09-13]
OMIM:619492	Cardiomyopathy, dilated, 2E		HP:0001644	PMID:30384889	PCS	HP:0011463	1/1			P	HPO:probinson[2021-09-13]
OMIM:619492	Cardiomyopathy, dilated, 2E		HP:0001644	PMID:31227780	PCS	HP:0003593	4/4			P	HPO:probinson[2021-09-13]
OMIM:613801	Retinitis pigmentosa 40		HP:0007737	PMID:7599633;PMID:8394174	PCS		7/7			P	HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0000662	PMID:8394174	PCS	HP:0011463	6/6			P	HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0000662	PMID:7599633	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0000518	PMID:7599633	PCS	HP:0003581	1/1			P	HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0011463	PMID:7599633;PMID:8394174	PCS		7/7			C	HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0008323	PMID:8394174	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0000007	PMID:8394174	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0000510	PMID:8394174	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613801	Retinitis pigmentosa 40		HP:0007843	PMID:7599633;PMID:8394174	PCS		7/7			P	HPO:probinson[2022-03-26]
OMIM:133020	Erythermalgia, primary		HP:0002014	OMIM:133020	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133020	Erythermalgia, primary		HP:0003621	PMID:14985375	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-03-24]
OMIM:133020	Erythermalgia, primary		HP:0001097	OMIM:133020	TAS					P	HPO:skoehler[2017-07-13]
OMIM:133020	Erythermalgia, primary		HP:0032147	PMID:14985375	PCS					P	HPO:lccarmody[2018-12-28]
OMIM:133020	Erythermalgia, primary		HP:0012332	OMIM:133020	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:133020	Erythermalgia, primary		HP:0012531	OMIM:133020	TAS					P	HPO:skoehler[2014-01-28]
OMIM:133020	Erythermalgia, primary		HP:0040264	OMIM:133020	TAS					P	HPO:skoehler[2017-07-13]
OMIM:133020	Erythermalgia, primary		HP:0000217	OMIM:133020	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133020	Erythermalgia, primary		HP:0000975	OMIM:133020	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133020	Erythermalgia, primary		HP:0000989	OMIM:133020	IEA					P	HPO:skoehler[2018-10-08]
OMIM:133020	Erythermalgia, primary		HP:0001962	OMIM:133020	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133020	Erythermalgia, primary		HP:0002019	OMIM:133020	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133020	Erythermalgia, primary		HP:0000006	PMID:14985375	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-24]
OMIM:133020	Erythermalgia, primary		HP:0000622	OMIM:133020	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133020	Erythermalgia, primary		HP:0003326	OMIM:133020	TAS					P	HPO:skoehler[2012-10-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000341	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0002465	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000582	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000486	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001251	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0003593	OMIM:616789	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001290	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001270	PMID:25167861	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0002719	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0011220	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000717	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000316	PMID:25167861	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001669	OMIM:616789	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000414	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0030084	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000158	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000311	PMID:25167861	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000154	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001762	OMIM:616789	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000232	PMID:25167861	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000194	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001260	PMID:25167861	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001263	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000470	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0005280	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000400	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0002007	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001357	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000006	PMID:25758992	PCS					I	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000369	PMID:25167861	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000589	PMID:25167861	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000028	PMID:25758992	PCS					P	HPO:probinson[2017-06-17]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000325	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0000248	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616789	Impaired intellectual development and distinctive facial features with or without cardiac defects		HP:0001655	OMIM:616789	TAS					P	HPO:skoehler[2017-07-13]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0002110	PMID:37725231	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0002099	PMID:37725231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0011463	PMID:37725231	PCS		1/2			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0011462	PMID:37725231	PCS		1/2			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0002837	PMID:37725231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0000007	PMID:37725231	PCS					I	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0031245	PMID:37725231	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0002090	PMID:37725231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0100750	PMID:37725231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0033524	PMID:37725231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0032558	PMID:37725231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621125	Ciliary dyskinesia, primary, 54		HP:0032559	PMID:37725231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0010628	OMIM:607684	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0003431	OMIM:607684	TAS				HP:0012825	P	HPO:probinson[2012-03-12]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0003376	PMID:18758688	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001178	OMIM:607684	TAS					P	HPO:probinson[2009-02-17]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0003693	PMID:18758688	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001371	OMIM:607684	TAS					P	HPO:skoehler[2015-07-26]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0002460	OMIM:607684	TAS					P	HPO:probinson[2013-12-14]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001270	OMIM:607684	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0011463	PMID:18758688	PCS		1/2			C	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0007340	PMID:18758688	PCS		2/2			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0009025	OMIM:607684	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0009027	OMIM:607684	TAS					P	HPO:probinson[2009-02-17]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0002936	PMID:18758688	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0000218	OMIM:607684	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0002359	PMID:18758688	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001765	PMID:18758688	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0007328	PMID:18758688	PCS		2/2			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001265	PMID:18758688	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0003621	PMID:18758688	PCS		1/2			C	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0002650	OMIM:607684	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0008959	PMID:18758688	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001288	PMID:18758688	PCS		2/2			P	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001761	PMID:18758688	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0003383	PMID:18758688	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0001284	PMID:18758688	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0009053	PMID:18758688	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0009130	PMID:18758688	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0007230	PMID:18758688	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0000508	OMIM:607684	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0006886	PMID:18758688	PCS		2/2			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0000006	PMID:18758688	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-11]
OMIM:607684	Charcot-Marie-Tooth disease, axonal, type 2E		HP:0003798	OMIM:607684	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:164150	Nystagmus, hereditary vertical		HP:0007670	OMIM:164150	TAS					P	HPO:probinson[2012-07-28]
OMIM:164150	Nystagmus, hereditary vertical		HP:0001251	OMIM:164150	TAS				HP:0012825	P	HPO:skoehler[2010-06-20]
OMIM:164150	Nystagmus, hereditary vertical		HP:0010544	OMIM:164150	TAS					P	HPO:skoehler[2010-06-18]
OMIM:164150	Nystagmus, hereditary vertical		HP:0000006	OMIM:164150	TAS					I	HPO:probinson[2009-02-17]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0002223	PMID:21178588;PMID:20358587	PCS		12/13			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000286	PMID:18042262	PCS		2/2			P	HPO:probinson[2020-07-23]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000341	PMID:20358587	PCS					P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000486	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0002046	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0004322	PMID:20358587;PMID:16439621	PCS		5/10			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001252	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0003593	PMID:21178588	PCS		2/3			C	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0008070	PMID:20358587	PCS		11/11			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0033725	PMID:16439621	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000518	PMID:16439621	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000639	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000957	PMID:20358587	PCS		3/9			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0011463	PMID:21178588	PCS		1/3			C	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001646	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000975	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000972	PMID:21178588	PCS		3/3			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000653	PMID:21178588	PCS		1/3			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001642	PMID:21178588;PMID:20358587	PCS		6/14			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000974	PMID:21178588	PCS		2/3			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000336	PMID:18042262	PCS		2/2			P	HPO:probinson[2020-07-23]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001028	PMID:20358587	PCS		2/9			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0002212	PMID:21178588;PMID:20358587	PCS		14/14			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000275	PMID:18042262	PCS		2/2			P	HPO:probinson[2020-07-23]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001561	PMID:21178588	PCS		2/3			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001003	PMID:21178588	PCS		3/3			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0002650	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001321	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000276	PMID:18042262	PCS		2/2			P	HPO:probinson[2020-07-23]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001382	PMID:21178588	PCS		1/3			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0001263	PMID:21178588;PMID:16439621	PCS		3/4			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0005144	PMID:16439621	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0002293	PMID:21178588	PCS		1/3			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000609	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0032152	PMID:20358587	PCS		5/9			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000506	PMID:20358587	PCS					P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000508	PMID:18042262	PCS		2/2			P	HPO:probinson[2020-07-23]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000767	PMID:20358587	PCS		1/9			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000348	PMID:20358587	PCS					P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000824	PMID:16439621	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000006	PMID:18042262	PCS					I	HPO:probinson[2020-07-23]
OMIM:615280	Cardiofaciocutaneous syndrome 4		HP:0000545	PMID:16439621	PCS		1/1			P	HPO:skoehler[2015-08-27];HPO:probinson[2022-04-11]
OMIM:613829	Leber congenital amaurosis 7		HP:0000550	PMID:9537410	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0000563	OMIM:613829	IEA					P	HPO:probinson[2013-08-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0000518	OMIM:613829	IEA					P	HPO:probinson[2013-08-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0000639	PMID:9537410	PCS		2/2			P	HPO:probinson[2022-03-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0012043	OMIM:613829	IEA					P	HPO:probinson[2013-08-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0003593	PMID:9537410	IEA		2/2			C	HPO:probinson[2022-03-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0000613	OMIM:613829	IEA				HP:0012828	P	HPO:probinson[2013-08-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0000007	PMID:9537410	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-03-10]
OMIM:613829	Leber congenital amaurosis 7		HP:0000505	PMID:9537410	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-10]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0002301	OMIM:614820	TAS				HP:0025303	P	HPO:skoehler[2013-06-06]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0002133	OMIM:614820	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0000496	OMIM:614820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001266	OMIM:614820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001332	OMIM:614820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001250	OMIM:614820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001260	OMIM:614820	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001263	OMIM:614820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001251	OMIM:614820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0200072	OMIM:614820	TAS					P	HPO:skoehler[2013-05-31]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0000639	OMIM:614820	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001268	OMIM:614820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0000006	OMIM:614820	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0002445	OMIM:614820	TAS				HP:0025303	P	HPO:skoehler[2013-06-06]
OMIM:614820	Alternating hemiplegia of childhood 2		HP:0001249	OMIM:614820	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612289	Fontaine progeroid syndrome		HP:0002100	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000046	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0010648	PMID:29100093	PCS		4/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0004322	PMID:29100093	PCS		4/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000160	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0010808	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0004440	PMID:29100093	PCS		4/4			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0003196	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002020	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001290	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0012745	PMID:29100093	PCS		5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0006191	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000319	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0007165	PMID:29100094	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0005807	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001647	PMID:29100094	PCS	HP:0003577	1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0000316	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000998	PMID:29100093	PCS		5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000238	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001324	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001643	PMID:29100094	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0001522	PMID:29100094	PCS		2/4			C	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0000278	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000677	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000358	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000494	PMID:29100093	PCS		5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000252	PMID:29100093	PCS		3/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000054	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002750	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002079	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0011968	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000691	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0001582	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000294	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0011800	PMID:29100093	PCS		5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0005180	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0009891	PMID:29100093	PCS		5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000926	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001537	PMID:29100093	PCS	HP:0003577				P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0001537	PMID:29100094	PCS		3/4			P	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0002705	PMID:29100093	PCS		1/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000568	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0003758	PMID:29100094;PMID:29100093	PCS		8/9			P	HPO:probinson[2020-12-12];HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000405	PMID:29100093	PCS		3/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000444	PMID:29100094	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0002107	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000520	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001015	PMID:29100094	PCS		4/4			P	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0000006	PMID:29100093	PCS					I	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000248	PMID:29100093	PCS		5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000369	PMID:29100094;PMID:29100093	PCS	HP:0003577	8/9			P	HPO:probinson[2020-12-12];HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000325	PMID:29100094	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0003577	PMID:29100093	PCS					C	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0001792	PMID:29100094;PMID:29100093	PCS		8/9			P	HPO:probinson[2020-12-12];HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000343	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002089	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000540	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000260	PMID:29100093	PCS		3/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000260	PMID:29100094	PCS	HP:0003577	4/4			P	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0002561	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002162	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000262	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002282	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001508	PMID:29100093	PCS		5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0009882	PMID:29100094;PMID:29100093	PCS		7/9			P	HPO:probinson[2020-12-12];HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000337	PMID:29100093	PCS	HP:0011461	5/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0001627	PMID:29100093	PCS	HP:0003577	3/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0008038	PMID:29100093	PCS		5/5	FEMALE		P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000219	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000059	OMIM:612289	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612289	Fontaine progeroid syndrome		HP:0002557	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001545	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001320	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001562	PMID:29100094	PCS	HP:0011461	4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0001363	PMID:29100094	PCS		2/2			P	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0005247	PMID:29100093	PCS	HP:0003577				P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0002650	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001321	PMID:29100094	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0000232	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002092	PMID:29100094	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0002093	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0005280	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0100678	PMID:29100094;PMID:29100093	PCS		9/9			P	HPO:probinson[2020-12-12];HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0001518	PMID:29100094	PCS	HP:0003577	4/4			P	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0007495	PMID:29100094	PCS		4/4			P	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0002209	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0001712	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0002208	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0001511	PMID:29100093	PCS		4/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0001511	PMID:29100094	PCS	HP:0011461	4/4			P	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0001159	PMID:29100093	PCS	HP:0003577	3/5			P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000664	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0003811	PMID:29100094	PCS		2/4			C	HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0001631	OMIM:612289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0000028	PMID:29100094	PCS		2/2	MALE		P	HPO:skoehler[2019-04-18];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0000303	PMID:29100093	PCS					P	HP:probinson[2018-04-29]
OMIM:612289	Fontaine progeroid syndrome		HP:0000347	PMID:29100094	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:612289	Fontaine progeroid syndrome		HP:0001798	OMIM:612289	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:612289	Fontaine progeroid syndrome		HP:0004942	PMID:29100093	PCS		2/3			P	HP:probinson[2018-04-29]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0012265	PMID:23354437	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0002110	PMID:23354437	PCS		1/4			P	HPO:skoehler[2013-08-18];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0003593	PMID:23354437	PCS		1/4			C	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0033036	PMID:23354437	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0000403	PMID:23354437	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0000007	PMID:23354437	PCS					I	HPO:skoehler[2013-08-18];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0006532	PMID:23354437	PCS	HP:0003593	4/4			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0100750	PMID:23354437	PCS		1/4			P	HPO:skoehler[2013-08-18];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0011109	PMID:23354437	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0002643	PMID:23354437	PCS		1/4			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:615294	Ciliary dyskinesia, primary, 21		HP:0003623	PMID:23354437	PCS		3/4			C	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:277180	Vas deferens, congenital bilateral aplasia of		HP:0003251	PMID:7529962	PCS					P	HPO:probinson[2022-09-02]
OMIM:277180	Vas deferens, congenital bilateral aplasia of		HP:0000007	PMID:7529962	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:277180	Vas deferens, congenital bilateral aplasia of		HP:0012873	PMID:7529962	PCS					P	HPO:probinson[2022-09-02]
OMIM:277180	Vas deferens, congenital bilateral aplasia of		HP:0000027	PMID:7529962	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:248370	Mandibuloacral dysplasia		HP:0000287	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000320	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0003077	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0001371	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0003074	PMID:12075506	PCS		0/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0001805	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0011463	PMID:14627682	PCS		1/1			C	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000678	PMID:14627682;PMID:12075506	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0008897	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000956	PMID:14627682;PMID:12075506	PCS		10/10			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0200021	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000831	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0004334	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0003761	PMID:16278265	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2020-04-27]
OMIM:248370	Mandibuloacral dysplasia		HP:0001387	PMID:12075506	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0003124	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0002673	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000293	PMID:14627682	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0040270	PMID:12075506	PCS		9/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-04-27];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0012385	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000007	PMID:12075506	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0003758	PMID:12075506	PCS		9/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0003635	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000444	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000520	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000685	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0002987	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000842	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0001870	PMID:12075506	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0009839	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0001596	PMID:12075506	PCS			MALE		P	HPO:skoehler[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0002240	PMID:12075506	PCS		9/9			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0001070	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000418	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000938	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0009882	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0009125	PMID:14627682;PMID:12075506	PCS		11/11			P	HPO:probinson[2022-06-09];HPO:skoehler[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000218	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000894	PMID:14627682;PMID:12075506	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0001029	PMID:14627682	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0003621	OMIM:248370	IEA					C	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0000270	PMID:12075506	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0006480	PMID:12075506	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000905	OMIM:248370	IEA					P	HPO:iea[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0002209	OMIM:248370	TAS					P	HPO:skoehler[2009-02-17]
OMIM:248370	Mandibuloacral dysplasia		HP:0002645	PMID:14627682	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0001510	PMID:12075506	PCS	HP:0011463	9/9			P	HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000347	PMID:14627682;PMID:12075506	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09];HPO:probinson[2022-06-09]
OMIM:248370	Mandibuloacral dysplasia		HP:0000468	PMID:17848409	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2020-04-27]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0030953	PMID:33015733	PCS		2/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0003577	PMID:33015733	PCS		4/5			C	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000343	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000486	PMID:33015733	PCS		2/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0001310	PMID:33015733	PCS		3/4			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002064	PMID:33015733	PCS		2/4			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0003390	PMID:33015733	PCS		1/3			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0012407	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0012650	PMID:33015733	PCS		4/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000718	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000514	PMID:33015733	PCS		2/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000733	PMID:33015733	PCS		1/4			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0001349	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002119	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0009623	PMID:33015733	PCS		3/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000219	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002714	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0009943	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0003623	PMID:33015733	PCS		1/5			C	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0001347	PMID:33015733	PCS					P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002553	PMID:33015733	PCS		3/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000252	PMID:33015733	PCS		5/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002510	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002078	PMID:33015733	PCS		1/4			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002650	PMID:33015733	PCS		2/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002474	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0031936	PMID:33015733	PCS		5/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0003487	PMID:33015733	PCS		2/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002079	PMID:33015733	PCS		5/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0001684	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000193	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0004691	PMID:33015733	PCS		3/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0001181	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0001639	PMID:33015733	PCS		4/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000007	PMID:33015733	PCS					I	HPO:probinson[2021-02-01];HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0002307	PMID:33015733	PCS		2/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0001510	PMID:33015733	PCS		5/5			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0007018	PMID:33015733	PCS		3/4			P	HPO:probinson[2021-02-01]
OMIM:619121	Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities		HP:0000322	PMID:33015733	PCS		1/5			P	HPO:probinson[2021-02-01]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0003577	PMID:25521379	PCS		5/5			C	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000340	PMID:25521379	PCS		1/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000463	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001250	PMID:25521379	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001272	PMID:25521379	PCS		2/4			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001270	PMID:25521379	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0002280	PMID:25521379	PCS		2/4			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0045028	OMIM:616212	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0007165	PMID:25521379	PCS		1/4			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000954	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000414	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0002119	PMID:25521379	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000219	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001302	PMID:25521379	PCS		2/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0006610	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001347	PMID:25521379	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000154	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000252	PMID:25521379	PCS		5/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0002079	OMIM:616212	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001263	PMID:25521379	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001182	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0002509	PMID:25521379	TAS		1/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001339	OMIM:616212	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000007	PMID:25521379	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001338	PMID:25521379	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0007874	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000400	PMID:25521379	PCS		2/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000664	PMID:25521379	PCS		2/5			P	HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0001257	PMID:25521379	PCS		2/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0002126	OMIM:616212	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0009879	PMID:25521379	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-11]
OMIM:616212	Lissencephaly 6, with microcephaly		HP:0000687	PMID:25521379	PCS		1/5			P	HPO:probinson[2021-05-11]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0003621	PMID:27857528	PCS		1/1			C	HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0002653	PMID:27857528	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000365	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0001442	PMID:18489744	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0002893	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000870	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0200008	OMIM:174800	TAS					P	HPO:skoehler[2013-06-11]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0004493	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0040084	PMID:27857528	PCS		0/1			P	HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:6000657	PMID:25719192	PCS					P	HPO:probinson[2024-05-09]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0040085	PMID:27857528	PCS		0/1			P	HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0010735	PMID:18489744;PMID:27857528	PCS		11/11			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-03];HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:6000869	PMID:27857528	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000826	PMID:18489744	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000836	PMID:27857528	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0033794	OMIM:174800	TAS					P	HPO:probinson[2021-05-08];HPO:probinson[2022-07-10]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000618	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000843	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000845	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0005605	PMID:18489744;PMID:27857528	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03];HPO:probinson[2024-08-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0003118	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0002756	PMID:18489744	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:174800	McCune-Albright syndrome, somatic, mosaic		HP:0000324	OMIM:174800	IEA					P	HPO:iea[2009-02-17]
OMIM:187750	Thoracic dysostosis, isolated		HP:0001591	OMIM:187750	IEA					P	HPO:skoehler[2009-02-17]
OMIM:187750	Thoracic dysostosis, isolated		HP:0000767	OMIM:187750	IEA					P	HPO:skoehler[2009-02-17]
OMIM:187750	Thoracic dysostosis, isolated		HP:0002205	OMIM:187750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:187750	Thoracic dysostosis, isolated		HP:0000773	OMIM:187750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:187750	Thoracic dysostosis, isolated		HP:0000006	OMIM:187750	IEA					I	HPO:skoehler[2009-02-17]
OMIM:612712	Leber congenital amaurosis 13		HP:0007737	PMID:15258582	PCS					P	HPO:probinson[2022-09-06]
OMIM:612712	Leber congenital amaurosis 13		HP:0011463	PMID:15258582	PCS					C	HPO:probinson[2022-09-06]
OMIM:612712	Leber congenital amaurosis 13		HP:0000007	PMID:15258582	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-06]
OMIM:612712	Leber congenital amaurosis 13		HP:0007663	PMID:15258582	PCS					P	HPO:probinson[2022-09-06]
OMIM:612712	Leber congenital amaurosis 13		HP:0000543	PMID:15258582	PCS					P	HPO:probinson[2022-09-06]
OMIM:612712	Leber congenital amaurosis 13		HP:0007843	PMID:15258582	PCS					P	HPO:probinson[2022-09-06]
OMIM:612712	Leber congenital amaurosis 13		HP:0000556	PMID:15258582	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-09-06]
OMIM:612712	Leber congenital amaurosis 13		HP:0000006	OMIM:612712	TAS					I	HPO:skoehler[2019-02-22];HPO:probinson[2022-09-06]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000286	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0002389	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001355	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001250	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001252	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001290	OMIM:602501	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0100790	OMIM:602501	TAS					P	HPO:skoehler[2013-01-22]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0004481	OMIM:602501	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0010442	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001909	OMIM:602501	TAS					P	HPO:skoehler[2013-01-22]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001629	OMIM:602501	TAS					P	HPO:skoehler[2012-12-03]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000319	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000316	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0002858	OMIM:602501	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001548	OMIM:602501	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000337	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000238	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0002119	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0003745	OMIM:602501	IEA					I	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001249	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0009748	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000494	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001442	PMID:22729224	PCS					I	HPO:skoehler[2012-12-03];HPO:probinson[2023-05-08]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001382	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001263	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0005280	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000965	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0000568	OMIM:602501	TAS					P	HPO:skoehler[2013-01-22]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0002667	OMIM:602501	TAS					P	HPO:skoehler[2013-01-22]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0001159	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602501	Megalencephaly-capillary malformation-polymicrogyria syndrome, somatic		HP:0002126	OMIM:602501	IEA					P	HPO:skoehler[2010-06-19]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0008936	PMID:30975617	PCS		6/6			P	HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0000750	PMID:28971144;PMID:30975617	PCS		5/8			P	HPO:probinson[2022-02-18];HPO:probinson[2022-02-18];HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0001332	PMID:28971144;PMID:30975617	PCS		8/8			P	HPO:probinson[2022-02-18];HPO:probinson[2022-02-18];HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0001260	PMID:30975617	PCS		6/6			P	HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0000007	PMID:28971144	PCS					I	HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0000821	PMID:30975617	PCS		2/6			P	HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0001270	PMID:30975617	PCS		4/6			P	HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0001638	PMID:30975617	PCS		1/6			P	HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0002359	PMID:28971144	PCS		1/2			P	HPO:probinson[2022-02-18];HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0001337	PMID:30975617	PCS		2/6			P	HPO:probinson[2022-02-18]
OMIM:619647	Dyskinesia with orofacial involvement, autosomal recessive		HP:0001336	PMID:28971144;PMID:30975617	PCS		5/8			P	HPO:probinson[2022-02-18];HPO:probinson[2022-02-18];HPO:probinson[2022-02-18]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002067	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002063	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002141	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002185	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000737	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000613	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0200147	OMIM:609454	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000658	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002439	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002015	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000651	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0001300	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002530	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002354	OMIM:609454	PCS					P	HPO:probinson[2012-03-18]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0001260	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002174	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002171	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000605	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002528	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002529	OMIM:609454	PCS		20/20			P	HPO:probinson[2012-03-18];HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002527	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000741	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002304	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000006	OMIM:609454	IEA					I	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000622	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0000743	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:609454	Supranuclear palsy, progressive, 2		HP:0002544	OMIM:609454	IEA					P	HPO:iea[2009-02-17]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0002133	PMID:31056671	PCS		1/2			P	HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0002079	PMID:31056671	PCS		2/2			P	HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0001250	PMID:31056671	PCS	HP:0003593	2/2			P	HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0002120	PMID:31056671	PCS		1/2			P	HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0001263	PMID:31056671	PCS		2/2			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0005484	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0032794	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0001290	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0025190	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0001270	PMID:31056671	PCS		2/2		HP:0012828	P	HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0032786	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0032792	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0000717	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0006892	PMID:31056671	PCS		1/2			P	HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0003429	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0001257	PMID:29961870	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618559	Epileptic encephalopathy, early infantile, 79		HP:0000006	PMID:31056671	PCS					I	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:600316	Deafness, neurosensory, autosomal recessive 3		HP:0003577	PMID:17851452	PCS					C	HPO:probinson[2022-06-01]
OMIM:600316	Deafness, neurosensory, autosomal recessive 3		HP:0000007	PMID:17851452	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-06-01]
OMIM:600316	Deafness, neurosensory, autosomal recessive 3		HP:0011476	PMID:17851452	PCS	HP:0003577				P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-01]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0002540	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0002188	PMID:32099069	PCS		4/11			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001332	PMID:32099069	PCS		7/13			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0002186	PMID:32099069	PCS		7/13			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0003593	PMID:32099069	PCS					C	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001270	PMID:32099069	PCS		13/13			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0033725	PMID:32099069	PCS		1/11			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0000514	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0007149	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0007325	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0007305	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001347	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0002179	PMID:32099069;PMID:28334938	PCS		6/12		HP:0025153;HP:0025153	P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0008936	PMID:32099069	PCS		8/12			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0000750	PMID:32099069	PCS		12/13			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001300	PMID:32099069	PCS					P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001266	PMID:32099069;PMID:28334938	PCS		11/11			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0008959	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0002395	PMID:32099069	PCS		10/12			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001260	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001285	PMID:28334938	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001263	PMID:32099069	PCS		7/11			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0007350	PMID:32099069	PCS		7/12			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0000007	PMID:28334938	PCS					I	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001338	PMID:32099069	PCS		1/11			P	HPO:probinson[2022-02-14]
OMIM:619653	Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus		HP:0001257	PMID:32099069;PMID:28334938	PCS		11/13			P	HPO:probinson[2022-02-14]
OMIM:606773	Hemifacial myohyperplasia, somatic		HP:0003577	PMID:37712948	PCS		5/5			C	HPO:probinson[2024-07-19]
OMIM:606773	Hemifacial myohyperplasia, somatic		HP:0004411	PMID:37712948	PCS		3/5			P	HPO:probinson[2024-07-19]
OMIM:606773	Hemifacial myohyperplasia, somatic		HP:0001442	PMID:37712948	PCS					I	HPO:probinson[2024-07-19]
OMIM:606773	Hemifacial myohyperplasia, somatic		HP:0005323	PMID:37712948	PCS		5/5			P	HPO:probinson[2024-07-19]
OMIM:606773	Hemifacial myohyperplasia, somatic		HP:0000508	PMID:37712948	PCS		4/5			P	HPO:probinson[2024-07-19]
OMIM:606773	Hemifacial myohyperplasia, somatic		HP:0045025	PMID:37712948	PCS		4/5			P	HPO:probinson[2024-07-19]
OMIM:606773	Hemifacial myohyperplasia, somatic		HP:0010751	PMID:37712948	PCS		5/5			P	HPO:probinson[2024-07-19]
OMIM:234250	Hall-Riggs syndrome		HP:0000286	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000463	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0001156	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0001250	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0010806	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0100255	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000939	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0001508	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0006297	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000316	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0008872	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0006334	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000179	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0001249	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0003301	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000252	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0001344	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0002650	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0002750	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0005280	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0002808	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000926	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000448	OMIM:234250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0000007	OMIM:234250	IEA					I	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0001511	OMIM:234250	IEA					P	HPO:iea[2009-02-17]
OMIM:234250	Hall-Riggs syndrome		HP:0006347	OMIM:234250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614377	Nephronophthisis 13		HP:0003774	PMID:22019273	PCS		3/4			P	HPO:skoehler[2013-05-29];HPO:probinson[2022-06-23]
OMIM:614377	Nephronophthisis 13		HP:0003774	PMID:23559409	PCS	HP:0011463	2/2			P	HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0003774	PMID:25726036	PCS		4/4			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0003621	PMID:25726036	PCS		3/4			C	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0000089	PMID:22019273	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-23]
OMIM:614377	Nephronophthisis 13		HP:0032948	PMID:22019273	PCS		2/4			P	HPO:probinson[2022-06-23]
OMIM:614377	Nephronophthisis 13		HP:0000096	PMID:22019273	PCS		2/4			P	HPO:probinson[2022-06-23]
OMIM:614377	Nephronophthisis 13		HP:0000090	PMID:22019273	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-06-23]
OMIM:614377	Nephronophthisis 13		HP:0033149	PMID:25726036;PMID:23559409	PCS		6/6			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0000093	PMID:25726036	PCS		2/2			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0033601	PMID:25726036	PCS		2/2			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0033867	PMID:25726036	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0012595	PMID:22019273	PCS		1/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-06-23]
OMIM:614377	Nephronophthisis 13		HP:0011463	PMID:23559409	PCS		2/2			C	HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0011461	PMID:25726036	PCS		1/4			C	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0000007	PMID:22019273	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-23]
OMIM:614377	Nephronophthisis 13		HP:0001407	PMID:23559409	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0001737	PMID:25726036	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0004737	PMID:25726036	PCS		2/2			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:614377	Nephronophthisis 13		HP:0001510	PMID:22019273	PCS		1/4			P	HPO:probinson[2022-06-23]
OMIM:266270	Ramon syndrome		HP:0004325	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000189	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000365	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000684	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0001014	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0002650	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0004322	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0001250	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0001492	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000580	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0005681	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0002808	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0008683	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000998	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0001009	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000007	OMIM:266270	IEA					I	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000169	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000543	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0001249	OMIM:266270	IEA					P	HPO:iea[2009-02-17]
OMIM:266270	Ramon syndrome		HP:0000962	OMIM:266270	IEA					P	HPO:skoehler[2010-06-20]
OMIM:230750	Gastroschisisabdominal wall defects, included		HP:0000007	OMIM:230750	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:230750	Gastroschisisabdominal wall defects, included		HP:0001426	OMIM:230750	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:230750	Gastroschisisabdominal wall defects, included		HP:0001543	OMIM:230750	IEA					P	HPO:iea[2009-02-17]
OMIM:230750	Gastroschisisabdominal wall defects, included		HP:0010866	OMIM:230750	TAS					P	HPO:nvasilevsky[2019-03-11]
OMIM:617118	Epilepsy, familial focal, with variable foci 3		HP:0032052	PMID:26285051	IEA		3/6			P	HPO:nvasilevsky[2018-09-17]
OMIM:617118	Epilepsy, familial focal, with variable foci 3		HP:0001250	OMIM:617118	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617118	Epilepsy, familial focal, with variable foci 3		HP:0003829	OMIM:617118	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617118	Epilepsy, familial focal, with variable foci 3		HP:0032046	PMID:27173016	PCS		2/15			P	HPO:nvasilevsky[2018-09-17]
OMIM:617118	Epilepsy, familial focal, with variable foci 3		HP:0000006	OMIM:617118	TAS					I	HPO:skoehler[2017-07-13]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0003577	PMID:31712251	PCS		2/2			C	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000463	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000260	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23];HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0002384	PMID:31712251	PCS	HP:0011463	1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0003031	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0004482	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0010105	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0010034	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0011220	PMID:31712251	PCS		1/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000316	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0006695	PMID:31712251	PCS		1/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0008897	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000219	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0025336	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0001522	PMID:31712251	PCS		1/2			C	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0001249	PMID:31712251	IEA		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0006118	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0001320	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0002553	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23];HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0032989	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000494	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0003022	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0032388	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0011344	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0010655	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0100856	PMID:31712251	PCS		1/1			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000007	PMID:31712251	PCS					I	HPO:probinson[2021-01-23];HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000568	PMID:31712251	PCS		1/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000028	PMID:31712251	PCS		1/1	MALE		P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000347	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:619135	Ritscher-Schinzel syndrome 3		HP:0000567	PMID:31712251	PCS		2/2			P	HPO:probinson[2021-01-23]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001034	PMID:36866916	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0002861	OMIM:278700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0003079	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001251	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001009	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0002936	PMID:34484303	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000656	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001268	OMIM:278700	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001249	OMIM:278700	PCS					P	HPO:probinson[2012-03-18]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001029	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0003623	PMID:36866916	PCS		1/1			C	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001265	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0003621	PMID:34484303	PCS		1/1			C	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000252	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000992	PMID:36866916	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0004334	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001266	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001761	PMID:34484303	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000491	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0006739	PMID:36866916	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000407	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0034275	PMID:34484303	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000509	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000007	PMID:2234061	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0030350	PMID:36866916	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0001257	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:278700	Xeroderma pigmentosum, complementation group A		HP:0000621	OMIM:278700	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0002025	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000286	OMIM:607323	PCS				HP:0012825	P	HPO:probinson[2012-03-31]
OMIM:607323	Duane-Radial ray syndrome		HP:0002023	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000486	OMIM:607323	TAS	HP:0003577				P	HP:probinson[2018-09-01]
OMIM:607323	Duane-Radial ray syndrome		HP:0000089	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000480	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000085	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0010048	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000518	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000316	OMIM:607323	PCS				HP:0012825	P	HPO:probinson[2012-03-31]
OMIM:607323	Duane-Radial ray syndrome		HP:0000634	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0002617	OMIM:607323	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607323	Duane-Radial ray syndrome		HP:0007766	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0001763	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0004712	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000453	PMID:23234485	IEA					P	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:607323	Duane-Radial ray syndrome		HP:0000452	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0100258	OMIM:607323	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0001739	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000407	PMID:12395297	PCS		2/13			P	HPO:probinson[2012-03-31];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0002949	PMID:12395297	PCS		1/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0009016	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000568	OMIM:607323	IEA		95%			P	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:607323	Duane-Radial ray syndrome		HP:0009777	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0001852	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0009778	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0003834	PMID:12395297	PCS		5/5			P	HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0000006	PMID:23234485	PCS					I	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:607323	Duane-Radial ray syndrome		HP:0002984	PMID:12395297	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0000324	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000126	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0001199	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0010628	OMIM:607323	PCS					P	HPO:probinson[2012-03-31]
OMIM:607323	Duane-Radial ray syndrome		HP:0003577	PMID:12395297	PCS		13/13			C	HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0000661	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0003298	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0005792	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0001629	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000619	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0009486	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000612	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0004736	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0008998	PMID:12395297	PCS		1/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0009921	PMID:12395297	PCS		12/13			P	HPO:iea[2009-02-17];HP:probinson[2018-09-01];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0000076	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0002650	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0001245	PMID:12395297	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0003022	PMID:12395297	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0002251	PMID:12395297	PCS		1/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:607323	Duane-Radial ray syndrome		HP:0008588	PMID:12843316	IEA		HP:0040283			P	HPO:probinson[2012-03-31]
OMIM:607323	Duane-Radial ray syndrome		HP:0001159	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0001631	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000542	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0003974	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:607323	Duane-Radial ray syndrome		HP:0000104	OMIM:607323	IEA					P	HPO:iea[2009-02-17]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002465	OMIM:608776	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002188	PMID:26453364;PMID:15945070	PCS		4/4			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001250	PMID:26453364;PMID:15148656;PMID:15945070	PCS		5/5			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001252	PMID:15148656;PMID:15945070	PCS		2/2			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0003196	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0003593	PMID:15148656	PCS		2/2			C	HPO:probinson[2024-03-13];HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0003073	PMID:15945070	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001929	PMID:15945070	PCS		1/1			P	HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000316	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000113	PMID:26453364	PCS		0/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001249	PMID:26453364	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0003642	PMID:15148656	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000252	PMID:26453364;PMID:15148656	PCS		4/5			P	HPO:probinson[2024-03-13];HPO:skoehler[2018-10-08]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001541	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002750	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001263	PMID:26453364;PMID:15148656;PMID:15945070	PCS		5/5			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002827	PMID:26453364	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000007	PMID:15945070	PCS					I	HPO:probinson[2017-06-25]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001976	PMID:15945070	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000565	PMID:15945070	PCS		1/1			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001698	PMID:26453364;PMID:15945070	PCS		2/5			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000248	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000369	PMID:26453364	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000343	PMID:26453364	PCS		0/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001272	PMID:26453364	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002283	PMID:15945070	PCS		1/1			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002240	PMID:15148656;PMID:15945070	PCS		2/2			P	HPO:probinson[2024-03-13];HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001508	PMID:26453364;PMID:15945070	PCS		4/5			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0009125	PMID:15945070	PCS		0/1			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001789	PMID:26453364	PCS		0/4			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0006610	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001744	PMID:15945070	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001347	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002652	PMID:26453364	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000154	PMID:26453364	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0025672	PMID:26453364	PCS	HP:0030674	1/4			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002059	PMID:26453364	PCS		3/3			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0003146	PMID:15945070	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002099	PMID:15148656	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0003186	PMID:15945070	PCS		1/1			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0000470	PMID:26453364	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0005280	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002808	PMID:26453364	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0011473	PMID:15945070	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001999	PMID:15945070	PCS		0/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001558	PMID:26453364	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0200134	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0002007	PMID:26453364	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-13]
OMIM:608776	Congenital disorder of glycosylation, type Il		HP:0001631	PMID:26453364	PCS		1/4			P	HPO:probinson[2024-03-13]
OMIM:615041	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10		HP:0003577	PMID:23217329	PCS		9/9			C	HPO:probinson[2023-03-29]
OMIM:615041	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10		HP:0007260	PMID:23217329	PCS		9/9			P	HPO:skoehler[2013-02-25]
OMIM:615041	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10		HP:0000133	PMID:23217329	PCS		5/8			P	HPO:skoehler[2013-02-25]
OMIM:615041	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10		HP:0007033	PMID:23217329	PCS		9/9			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-29]
OMIM:615041	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10		HP:0045005	PMID:23217329	PCS		5/8			P	HPO:probinson[2023-03-29]
OMIM:615041	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10		HP:0000007	PMID:23217329	PCS					I	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-29]
OMIM:615041	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10		HP:0007973	PMID:23217329	PCS		6/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-29]
OMIM:231300	Glaucoma 3, primary congenital, A		HP:0008041	OMIM:231300	IEA					P	HPO:iea[2009-02-17]
OMIM:231300	Glaucoma 3, primary congenital, A		HP:0007906	OMIM:231300	IEA					P	HPO:iea[2009-02-17]
OMIM:231300	Glaucoma 3, primary congenital, A		HP:0003593	PMID:9097971	PCS					C	HPO:probinson[2021-08-16]
OMIM:231300	Glaucoma 3, primary congenital, A		HP:0000007	PMID:9097971	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-08-16]
OMIM:231300	Glaucoma 3, primary congenital, A		HP:0000557	OMIM:231300	IEA					P	HPO:iea[2009-02-17]
OMIM:102000	Acroleukopathy, symmetric		HP:0200015	OMIM:102000	IEA					P	HPO:iea[2009-02-17]
OMIM:102000	Acroleukopathy, symmetric		HP:0000006	OMIM:102000	IEA					I	HPO:iea[2009-02-17]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0031329	PMID:9563954	PCS		2/2			P	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0031318	PMID:9563954	PCS		0/2			P	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0003621	PMID:9563954	PCS		2/5			C	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0031319	PMID:9563954	PCS		2/2			P	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0003596	PMID:9563954	PCS		1/5			C	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0030682	OMIM:613424	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0033755	PMID:9563954	PCS		6/8			P	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0011463	PMID:9563954	PCS		1/5			C	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0011462	PMID:9563954	PCS		1/5			C	HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0001635	OMIM:613424	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0001712	OMIM:613424	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0001723	OMIM:613424	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0004308	OMIM:613424	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0000006	PMID:9563954	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-03]
OMIM:613424	Cardiomyopathy, dilated, 1R		HP:0001644	PMID:9563954	PCS		5/8			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-07-03]
OMIM:186300	Syndactyly, type V		HP:0001156	OMIM:186300	TAS					P	HPO:probinson[2012-06-08]
OMIM:186300	Syndactyly, type V		HP:0006185	OMIM:186300	IEA					P	HPO:iea[2009-02-17]
OMIM:186300	Syndactyly, type V		HP:0009473	OMIM:186300	IEA					P	HPO:iea[2009-02-17]
OMIM:186300	Syndactyly, type V		HP:0100490	OMIM:186300	TAS					P	HPO:probinson[2012-06-08]
OMIM:186300	Syndactyly, type V		HP:0001032	OMIM:186300	IEA					P	HPO:iea[2009-02-17]
OMIM:186300	Syndactyly, type V		HP:0009882	OMIM:186300	IEA					P	HPO:iea[2009-02-17]
OMIM:186300	Syndactyly, type V		HP:0004692	OMIM:186300	TAS					P	HPO:probinson[2012-06-08]
OMIM:186300	Syndactyly, type V		HP:0010554	OMIM:186300	IEA					P	HPO:iea[2009-02-17]
OMIM:186300	Syndactyly, type V		HP:0009702	OMIM:186300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:186300	Syndactyly, type V		HP:0009779	OMIM:186300	TAS					P	HPO:probinson[2012-06-08]
OMIM:186300	Syndactyly, type V		HP:0000006	OMIM:186300	IEA					I	HPO:iea[2009-02-17]
OMIM:186300	Syndactyly, type V		HP:0005867	OMIM:186300	TAS					P	HPO:probinson[2012-06-08]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0006208	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0008905	OMIM:300863	TAS			FEMALE		P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0004322	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0004331	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0003196	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0003021	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0012789	OMIM:300863	TAS					P	HPO:probinson[2014-04-24]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000926	OMIM:300863	TAS				HP:0012828	P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000568	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000238	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000878	OMIM:300863	TAS		HP:0040283	MALE		P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0001511	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0002007	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0001423	PMID:20181727	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2022-03-27]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000883	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000256	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0006402	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0006028	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0002866	OMIM:300863	TAS			FEMALE		P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000369	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0000457	OMIM:300863	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300863	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia		HP:0001249	OMIM:300863	TAS		HP:0040283	FEMALE		P	HPO:skoehler[2012-10-14]
OMIM:608762	Epilepsy, idiopathic generalized, susceptibility to, 3		HP:0002069	OMIM:608762	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608762	Epilepsy, idiopathic generalized, susceptibility to, 3		HP:0000992	OMIM:608762	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608762	Epilepsy, idiopathic generalized, susceptibility to, 3		HP:0001250	OMIM:608762	IEA					P	HPO:skoehler[2015-01-27]
OMIM:608762	Epilepsy, idiopathic generalized, susceptibility to, 3		HP:0000007	OMIM:608762	TAS					I	HPO:skoehler[2012-10-17]
OMIM:617642	Polydactyly, postaxial, type A7		HP:0003577	PMID:28488682	PCS		4/4			C	HPO:probinson[2023-02-06]
OMIM:617642	Polydactyly, postaxial, type A7		HP:0001162	PMID:28488682	PCS		0/4			P	HPO:probinson[2023-02-06]
OMIM:617642	Polydactyly, postaxial, type A7		HP:0005709	PMID:28488682	PCS		1/4			P	HPO:probinson[2023-02-06]
OMIM:617642	Polydactyly, postaxial, type A7		HP:0000007	PMID:28488682	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617642	Polydactyly, postaxial, type A7		HP:0004704	PMID:28488682	PCS		1/4			P	HPO:probinson[2023-02-06]
OMIM:617642	Polydactyly, postaxial, type A7		HP:0001830	PMID:28488682	PCS		4/4			P	HPO:probinson[2023-02-06]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000286	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000483	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0002540	PMID:28763441	PCS		1/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000486	PMID:30622326	PCS		1/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000343	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0004322	PMID:28763441	IEA		3/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0002002	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0001250	PMID:28763441;PMID:30622326	PCS		1/8			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000480	PMID:30622326	PCS		1/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0001252	PMID:30622326	PCS		5/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0003196	PMID:30622326	PCS		1/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0410030	PMID:28763441	PCS		1/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000518	PMID:28763441;PMID:30622326	PCS		8/8			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0007068	PMID:28763441	PCS		1/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000316	PMID:28763441;PMID:30622326	PCS		7/8			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0001845	PMID:28763441;PMID:30622326	PCS		5/8			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000414	PMID:30622326	PCS		3/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0001627	PMID:28763441	PCS		1/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0002714	PMID:30622326	PCS		4/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000411	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000110	PMID:28763441	PCS		1/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000175	PMID:28763441	PCS		1/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0001344	PMID:28763441;PMID:30622326	PCS		8/8			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000431	PMID:30622326	PCS		4/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0002650	PMID:30622326	PCS		1/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0001288	PMID:28763441;PMID:30622326	PCS		7/8			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000293	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0001263	PMID:30622326	PCS		5/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000470	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0045025	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0011344	PMID:28763441	PCS		3/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0011228	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000308	PMID:30622326	PCS		4/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000729	PMID:30622326	PCS		3/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000767	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000007	PMID:28763441	PCS					I	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000568	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000268	PMID:28763441	PCS		3/3			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0002007	PMID:28763441;PMID:30622326	PCS		5/8			P	HPO:probinson[2020-05-23];HPO:probinson[2020-05-23];HPO:probinson[2020-05-23]
OMIM:618571	Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies		HP:0000369	PMID:30622326	PCS		2/5			P	HPO:probinson[2020-05-23]
OMIM:106500	Annular erythema		HP:0010783	OMIM:106500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:106500	Annular erythema		HP:0000006	OMIM:106500	IEA					I	HPO:iea[2009-02-17]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0005743	PMID:17663471	PCS		2/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0002650	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0004322	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0000089	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0005565	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0002750	PMID:17663471	PCS		1/1			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0012408	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0025466	PMID:17663471	PCS		3/3			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0011400	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0000093	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0033132	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-10-12]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0000938	PMID:17663471	PCS		3/3			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0000007	PMID:17663471	PCS					I	HPO:probinson[2020-09-09];HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0002119	PMID:17663471	IEA		4/4			P	HPO:probinson[2020-09-09]
OMIM:611555	Renal tubular acidosis, distal, with nephrocalcinosis, short stature, impaired intellectual development, and distinctive facies		HP:0001942	PMID:17663471	PCS		4/4			P	HPO:probinson[2020-09-09]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0003587	OMIM:182600	IEA					C	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0003621	PMID:12112092	PCS					C	HPO:probinson[2022-09-02]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0002650	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0002166	OMIM:182600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0000012	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0001761	OMIM:182600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0002079	OMIM:182600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0003487	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0000020	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0002064	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0002061	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0001270	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0010550	OMIM:182600	TAS					P	HPO:probinson[2012-04-28]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0007340	PMID:12112092	PCS		11/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-02]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0003828	OMIM:182600	IEA					M	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0002839	OMIM:182600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0003829	OMIM:182600	IEA					I	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0001258	OMIM:182600	IEA					P	HPO:skoehler[2015-01-27]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0000006	PMID:11685207	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0001347	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0008944	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:182600	Spastic paraplegia 3, autosomal dominant		HP:0002314	OMIM:182600	IEA					P	HPO:iea[2009-02-17]
OMIM:613342	Brachydactylous dwarfism, Mseleni type		HP:0003510	OMIM:613342	IEA					P	HPO:skoehler[2015-01-27]
OMIM:175505	Polyposis of gastric fundus without polyposis coli		HP:0004295	OMIM:175505	TAS					P	HPO:probinson[2015-02-22]
OMIM:175505	Polyposis of gastric fundus without polyposis coli		HP:0004394	OMIM:175505	TAS					P	HPO:probinson[2015-02-22]
OMIM:175505	Polyposis of gastric fundus without polyposis coli		HP:0000006	OMIM:175505	TAS					I	HPO:probinson[2009-02-17]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0000230	PMID:35281597	PCS		1/1			P	HPO:probinson[2009-02-17];HP:probinson[2019-02-27];HPO:probinson[2022-08-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0001058	PMID:12488604	PCS					P	HP:probinson[2019-02-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0005224	OMIM:116920	TAS					P	HPO:probinson[2012-04-26]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0005420	OMIM:116920	TAS					P	HPO:probinson[2009-02-17]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0011899	PMID:35281597	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0032434	PMID:35281597;PMID:12488604	PCS		6/6			P	HPO:probinson[2022-08-27];HP:probinson[2019-04-19]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0032435	PMID:3519653	PCS		HP:0040283			P	HP:probinson[2019-04-19]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0011227	PMID:35281597	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0002719	PMID:35281597	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0000704	OMIM:116920	TAS					P	HPO:probinson[2009-02-17]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0002728	PMID:35281597	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0002718	PMID:1347532	PCS		1/1			P	HP:probinson[2019-02-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0000007	PMID:12488604	PCS					I	HPO:probinson[2009-02-17];HP:probinson[2019-02-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0007499	OMIM:116920	TAS					P	HPO:probinson[2012-04-26]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0200042	PMID:26639818	PCS	HP:0011463	5/19			P	HP:probinson[2019-02-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0002028	PMID:35281597	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0001974	PMID:35281597;PMID:26639818;PMID:26497373	PCS		32/32			P	HPO:probinson[2022-08-27];HP:probinson[2019-02-27];HPO:probinson[2012-04-26];HP:probinson[2019-02-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0003623	PMID:35281597	PCS		1/1			C	HPO:probinson[2022-08-27]
OMIM:116920	Leukocyte adhesion deficiency, type I		HP:0002754	PMID:26497373	PCS		1/12			P	HP:probinson[2019-02-27]
OMIM:109800	Bladder cancer		HP:0001442	OMIM:109800	IEA					I	HPO:skoehler[2019-04-18]
OMIM:109800	Bladder cancer		HP:0006740	OMIM:109800	IEA					P	HPO:iea[2009-02-17]
OMIM:109800	Bladder cancer		HP:0000006	OMIM:109800	IEA					I	HPO:iea[2009-02-17]
OMIM:109800	Bladder cancer		HP:0009725	OMIM:109800	TAS					P	HPO:probinson[2022-09-08]
OMIM:610878	Vesicoureteral reflux 2		HP:0000076	PMID:17357069	PCS					P	HPO:probinson[2013-04-06]
OMIM:610878	Vesicoureteral reflux 2		HP:0000089	PMID:17357069	PCS					P	HPO:probinson[2013-04-06]
OMIM:610878	Vesicoureteral reflux 2		HP:0000006	PMID:17357069	PCS					I	HPO:probinson[2013-01-09]
OMIM:620763	Lisch epithelial corneal dystrophy		HP:0011463	PMID:37972748	PCS					C	HPO:probinson[2024-07-07]
OMIM:620763	Lisch epithelial corneal dystrophy		HP:0007709	PMID:37972748	PCS					P	HPO:probinson[2024-07-07]
OMIM:620763	Lisch epithelial corneal dystrophy		HP:0000006	PMID:37972748	PCS					I	HPO:probinson[2024-07-07]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0001022	OMIM:300650	TAS					P	HPO:probinson[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0000639	OMIM:300650	IEA					P	HPO:iea[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0007680	OMIM:300650	IEA					P	HPO:iea[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0001361	OMIM:300650	IEA					P	HPO:iea[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0000613	OMIM:300650	IEA					P	HPO:iea[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0005592	OMIM:300650	IEA					P	HPO:iea[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0000505	OMIM:300650	IEA					P	HPO:iea[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0001417	OMIM:300650	IEA					I	HPO:iea[2009-02-17]
OMIM:300650	Albinism, ocular, with late-onset sensorineural deafness		HP:0008615	OMIM:300650	IEA	HP:0003584				P	HPO:iea[2009-02-17]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000089	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0003155	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000518	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001409	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000319	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0012471	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0007485	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0011461	PMID:33060134	PCS		5/5			C	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000437	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0008850	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001888	PMID:33060134	PCS		4/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000878	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001643	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0004315	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002113	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000252	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001385	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0011968	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000691	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002194	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0012735	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0030828	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001182	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001738	PMID:33060134	PCS		1/4			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000007	PMID:33060134	PCS					I	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000568	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000369	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001655	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0030799	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0006528	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000581	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001395	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0008070	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002719	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001903	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0008551	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000337	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001747	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0006577	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002910	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002850	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001363	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000270	PMID:33060134	PCS		3/10			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002092	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0033677	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0011344	PMID:33060134	PCS		4/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002093	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0005280	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0010976	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000821	PMID:33060134	PCS		3/4			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001511	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002007	PMID:33060134	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0200055	PMID:33060134	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001873	PMID:33060134	PCS		4/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0001631	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000347	PMID:33060134	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0002720	PMID:33060134	PCS		3/5			P	HPO:probinson[2022-08-28]
OMIM:620005	Primordial dwarfism-immunodeficiency-lipodystrophy syndrome		HP:0000028	PMID:33060134	PCS		2/3			P	HPO:probinson[2022-08-28]
OMIM:137050	Gamma-A-Globulin, defect in assembly of		HP:0002205	OMIM:137050	TAS					P	HPO:probinson[2009-02-17]
OMIM:137050	Gamma-A-Globulin, defect in assembly of		HP:0000006	OMIM:137050	TAS					I	HPO:probinson[2009-02-17]
OMIM:137050	Gamma-A-Globulin, defect in assembly of		HP:0002720	OMIM:137050	TAS					P	HPO:probinson[2015-02-15]
OMIM:617871	Retinitis pigmentosa 81		HP:0007737	PMID:28973684	PCS		4/4			P	HPO:probinson[2023-02-20]
OMIM:617871	Retinitis pigmentosa 81		HP:0000662	PMID:28973684	PCS		4/4			P	HPO:probinson[2023-02-20]
OMIM:617871	Retinitis pigmentosa 81		HP:0011463	PMID:28973684	PCS		4/4			C	HPO:probinson[2023-02-20]
OMIM:617871	Retinitis pigmentosa 81		HP:0000007	PMID:28973684	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:617871	Retinitis pigmentosa 81		HP:0007663	PMID:28973684	PCS					P	HPO:probinson[2023-02-20]
OMIM:617871	Retinitis pigmentosa 81		HP:0000543	PMID:28973684	PCS		4/4			P	HPO:probinson[2023-02-20]
OMIM:617871	Retinitis pigmentosa 81		HP:0007843	PMID:28973684	PCS		4/4			P	HPO:probinson[2023-02-20]
OMIM:617871	Retinitis pigmentosa 81		HP:0007722	PMID:28973684	PCS		2/4			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:300888	Hypothyroidism, central, and testicular enlargement		HP:0033075	PMID:24108313	PCS		16/16			P	HPO:probinson[2021-02-25];HPO:probinson[2021-02-25]
OMIM:300888	Hypothyroidism, central, and testicular enlargement		HP:0001419	PMID:23143598	PCS					I	HPO:skoehler[2013-01-21];HPO:probinson[2021-02-25]
OMIM:300888	Hypothyroidism, central, and testicular enlargement		HP:0008202	PMID:24108313	PCS		16/24			P	HPO:probinson[2021-02-25]
OMIM:300888	Hypothyroidism, central, and testicular enlargement		HP:0000821	PMID:24108313	PCS		17/17			P	HPO:skoehler[2015-01-27];HPO:probinson[2021-02-25]
OMIM:300888	Hypothyroidism, central, and testicular enlargement		HP:0025502	OMIM:300888	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300888	Hypothyroidism, central, and testicular enlargement		HP:0033082	PMID:24108313	PCS					P	HPO:probinson[2021-02-25]
OMIM:256370	Nephrotic syndrome, type 4		HP:0003676	OMIM:256370	TAS					C	HPO:skoehler[2012-10-17]
OMIM:256370	Nephrotic syndrome, type 4		HP:0000100	OMIM:256370	IEA					P	HPO:iea[2009-02-17]
OMIM:256370	Nephrotic syndrome, type 4		HP:0000083	OMIM:256370	IEA					P	HPO:iea[2009-02-17]
OMIM:256370	Nephrotic syndrome, type 4		HP:0011463	OMIM:256370	TAS					C	HPO:probinson[2013-03-13]
OMIM:256370	Nephrotic syndrome, type 4		HP:0000097	OMIM:256370	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:256370	Nephrotic syndrome, type 4		HP:0001967	OMIM:256370	IEA					P	HPO:iea[2009-02-17]
OMIM:256370	Nephrotic syndrome, type 4		HP:0002667	OMIM:256370	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256370	Nephrotic syndrome, type 4		HP:0000006	OMIM:256370	TAS					I	HPO:skoehler[2017-07-13]
OMIM:125440	Dentin dysplasia with sclerotic bones		HP:0000164	OMIM:125440	IEA					P	HPO:iea[2009-02-17]
OMIM:125440	Dentin dysplasia with sclerotic bones		HP:0005652	OMIM:125440	IEA					P	HPO:iea[2009-02-17]
OMIM:125440	Dentin dysplasia with sclerotic bones		HP:0011060	OMIM:125440	IEA					P	HPO:skoehler[2015-01-27]
OMIM:125440	Dentin dysplasia with sclerotic bones		HP:0000006	OMIM:125440	IEA					I	HPO:iea[2009-02-17]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0003477	PMID:27066569	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0005612	PMID:27066569	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0003577	PMID:34193129;PMID:27066569;PMID:31872057	PCS		3/3			C	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0001252	PMID:27066569	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0002460	PMID:27066569;PMID:31872057	PCS		2/2			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0033685	PMID:27066569	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0031189	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0012179	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0008112	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0040078	PMID:27066569;PMID:31872057	PCS		2/2			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0009027	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0006597	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0000218	PMID:27066569	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0002359	PMID:34193129	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0003202	PMID:34193129;PMID:31872057	PCS		2/2			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0001265	PMID:34193129	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0001762	PMID:27066569	PCS	HP:0003577	1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0002376	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0002098	PMID:27066569	PCS	HP:0003593	1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0002098	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0002098	PMID:34193129	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0005684	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0011948	PMID:27066569	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0001263	PMID:34193129	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0030207	PMID:27066569	PCS	HP:0003593	1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0009110	PMID:27066569	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0009830	PMID:34193129	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0000007	PMID:27066569	PCS					I	HPO:probinson[2022-09-04]
OMIM:620011	Spinal muscular atrophy, distal, autosomal recessive, 6		HP:0003438	PMID:31872057	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0007979	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000486	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0001272	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0032794	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0033128	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0033725	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0045074	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0012471	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000316	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000733	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0025336	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000311	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0003623	PMID:32105419	PCS		2/2			C	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0002059	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000431	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0031936	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0004330	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000294	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0011344	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000629	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000007	PMID:32105419	PCS					I	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0100716	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000648	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0001319	PMID:32105419	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619690	Brunet-Wagner neurodevelopmental syndrome		HP:0000666	PMID:32105419	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001276	PMID:29198722	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000486	PMID:29198722	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002120	PMID:29198722	PCS		1/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0003196	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001252	PMID:29198722	PCS	HP:0003593	7/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002020	PMID:29198722	PCS		4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0003593	PMID:29198722	PCS		7/7			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001251	PMID:29198722	PCS		5/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001270	PMID:29198722	PCS		7/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0011856	PMID:29198722	PCS		2/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000280	PMID:29198722	PCS		2/3			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0010761	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0040082	PMID:29198722	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0100033	PMID:29198722	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001508	PMID:29198722	PCS		2/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0100703	PMID:29198722	PCS		1/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0012172	PMID:29198722	PCS		1/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0011220	PMID:29198722	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002317	PMID:29198722	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002714	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000752	PMID:29198722	PCS		4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002019	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000256	PMID:29198722	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001249	PMID:29198722	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000336	PMID:29198722	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001265	PMID:29198722	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000253	PMID:29198722	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0008936	PMID:29198722	PCS		2/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002553	PMID:29198722	PCS					P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002136	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001344	PMID:29198722	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000574	PMID:29198722	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001762	PMID:29198722	PCS		1/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0031936	PMID:29198722	PCS					P	HPO:skoehler[2019-02-22];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000232	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0011968	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000194	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0001263	PMID:29198722	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0002191	PMID:29198722	PCS		3/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0005280	PMID:29198722	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000729	PMID:29198722	PCS		5/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0006288	PMID:29198722	PCS		2/7			P	HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000565	PMID:29198722	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000006	PMID:29198722	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-19]
OMIM:617865	Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features		HP:0000687	PMID:29198722	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-19]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0032979	PMID:38230350	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0025179	PMID:38230350	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0003593	PMID:38230350	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0002094	PMID:38230350	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0002092	PMID:38230350	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0002093	PMID:38230350	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0001508	PMID:38230350	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0001639	PMID:38230350	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0031185	PMID:38230350	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0011463	PMID:38230350	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0001708	PMID:38230350	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0033376	PMID:38230350	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0011462	PMID:38230350	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0000007	PMID:38230350	PCS					I	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0004749	PMID:38230350	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0000961	PMID:38230350	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0002104	PMID:38230350	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0001678	PMID:38230350	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0001667	PMID:38230350	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0001622	PMID:38230350	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620777	Pulmonary hypertension, primary, 6		HP:0005954	PMID:38230350	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:205700	Anemia, autoimmune hemolytic		HP:0001890	OMIM:205700	IEA					P	HPO:iea[2009-02-17]
OMIM:205700	Anemia, autoimmune hemolytic		HP:0001939	OMIM:205700	IEA					P	HPO:iea[2009-02-17]
OMIM:205700	Anemia, autoimmune hemolytic		HP:0000007	OMIM:205700	IEA					I	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001254	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001276	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0002013	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001250	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0410066	PMID:22626821;PMID:19551947	PCS		20/20			P	HPO:NicoleVasilevsky[2018-02-23];HPO:NicoleVasilevsky[2018-03-02]
OMIM:248600	Maple syrup urine disease		HP:6000124	PMID:32491705	PCS					P	HPO:probinson[2024-01-06]
OMIM:248600	Maple syrup urine disease		HP:0001252	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001251	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001290	OMIM:248600	TAS					P	HPO:skoehler[2017-07-13]
OMIM:248600	Maple syrup urine disease		HP:0002181	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0031796	OMIM:248600	IEA					C	HPO:skoehler[2018-10-08]
OMIM:248600	Maple syrup urine disease		HP:0000738	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001507	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0033155	PMID:7413299	PCS					P	HPO:probinson[2020-10-12]
OMIM:248600	Maple syrup urine disease		HP:0000007	OMIM:248600	IEA					I	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001943	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0008344	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0008872	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001946	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:4000207	OMIM:248600	TAS					P	HPO:probinson[2024-01-06]
OMIM:248600	Maple syrup urine disease		HP:0001249	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001733	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0001259	OMIM:248600	IEA					P	HPO:iea[2009-02-17]
OMIM:248600	Maple syrup urine disease		HP:0003128	OMIM:248600	TAS					P	HPO:probinson[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0005479	OMIM:308230	TAS				HP:0012828	P	HPO:probinson[2012-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002961	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002783	PMID:9255191	PCS		20/56			P	HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0003496	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0030991	PMID:9255191	PCS		11/56			P	HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001394	PMID:9255191	PCS		6/56			P	HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002240	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0003593	PMID:10228294	PCS		5/5			C	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0030812	OMIM:308230	TAS					P	HPO:skoehler[2017-07-13]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0034285	PMID:10228294	PCS		6/10			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-11]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001508	PMID:9255191	PCS		18/56			P	HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002959	OMIM:308230	TAS					P	HPO:probinson[2012-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002718	OMIM:308230	TAS					P	HPO:probinson[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0100806	PMID:9255191	PCS		8/56			P	HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0200123	OMIM:308230	TAS					P	HPO:skoehler[2015-12-30]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0020102	PMID:10228294	PCS		4/5			P	HPO:probinson[2022-06-04]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001744	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0004315	PMID:10228294	PCS		5/5		HP:0012828	P	HPO:probinson[2012-05-06];HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001347	PMID:10228294	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002014	PMID:9255191	PCS		31/56			P	HPO:iea[2009-02-17];HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001287	PMID:9255191	PCS		5/56			P	HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0000230	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002376	PMID:10228294	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0000155	PMID:9255191	PCS		25/56			P	HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0410243	PMID:10228294	PCS		0/5			P	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001263	PMID:10228294	PCS		3/4			P	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0003261	PMID:10228294	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0012418	PMID:10228294	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0012115	PMID:9255191	PCS		9/56		HP:0011010	P	HPO:skoehler[2013-06-10];HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0011448	PMID:10228294	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0009098	PMID:10228294	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0010280	OMIM:308230	IEA					P	HPO:skoehler[2010-06-20]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001419	PMID:9255191	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-05-19]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002849	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001878	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002847	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0005419	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001873	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002720	OMIM:308230	TAS				HP:0012828	P	HPO:probinson[2012-05-06]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0002721	OMIM:308230	IEA					P	HPO:iea[2009-02-17]
OMIM:308230	Immunodeficiency, X-linked, with hyper-IgM		HP:0001875	PMID:9255191;PMID:10228294	PCS		39/61			P	HPO:probinson[2009-02-17];HPO:probinson[2020-05-19];HPO:probinson[2022-05-06]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0004325	OMIM:617695	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0003577	PMID:28823707	PCS		1/7			C	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002023	PMID:28823707	PCS		1/7			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002540	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000486	PMID:28823707	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000540	PMID:28823707	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0004322	OMIM:617695	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001250	PMID:28823707	PCS		0/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001274	PMID:28823707	PCS		1/4			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001251	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0003593	PMID:28823707	PCS		6/7			C	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001290	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0040082	PMID:28823707	PCS		7/7			P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0012110	PMID:28823707	PCS		4/4			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000817	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000414	PMID:28823707	PCS		5/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000733	PMID:28823707	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001763	PMID:28823707	PCS		2/7			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001265	OMIM:617695	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002311	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0003202	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002136	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002015	OMIM:617695	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000252	OMIM:617695	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000750	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001762	PMID:28823707	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001321	PMID:28823707	PCS		4/4			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001288	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002079	PMID:28823707	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001260	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001263	PMID:28823707	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002070	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000729	PMID:28823707	PCS		2/4			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000007	PMID:28823707	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0100716	PMID:28823707	PCS		1/4			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000565	OMIM:617695	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000400	PMID:28823707	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0002205	OMIM:617695	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0007018	PMID:28823707	PCS		1/4			P	HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0001257	PMID:28823707	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617695	Pontocerebellar hypoplasia, type 11		HP:0000589	PMID:28823707	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:606798	Blepharospasm, benign essential, susceptibility to		HP:0003596	OMIM:606798	TAS					C	HPO:probinson[2009-02-17]
OMIM:606798	Blepharospasm, benign essential, susceptibility to		HP:0003745	OMIM:606798	TAS					I	HPO:probinson[2009-02-17]
OMIM:606798	Blepharospasm, benign essential, susceptibility to		HP:0000006	OMIM:606798	IEA					I	HPO:skoehler[2019-04-18]
OMIM:606798	Blepharospasm, benign essential, susceptibility to		HP:0000643	OMIM:606798	TAS					P	HPO:probinson[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000286	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002465	OMIM:253220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0003510	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0007957	PMID:26908836	PCS		19/30			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0034859	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-18]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000365	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0003311	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001376	PMID:26908836	PCS		22/26			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0004322	PMID:1702266;PMID:26908836	PCS		24/30			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001371	PMID:26908836	PCS		21/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0008807	PMID:26908836	PCS		15/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0003593	PMID:6813001;PMID:9099834	PCS		5/16			C	HPO:probinson[2022-02-01];HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000280	PMID:26908836	PCS		27/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002180	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0012307	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0011461	PMID:9099834	PCS		11/15			C	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000238	OMIM:253220	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0008897	PMID:6813001	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002857	PMID:26908836	PCS		17/27			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000158	PMID:26908836	PCS		16/25			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001840	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001007	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001249	PMID:1702266;PMID:26908836	PCS		25/30			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001540	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002870	PMID:26908836	PCS		7/20			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000574	PMID:26908836	PCS		13/25			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001387	PMID:26908836	PCS		18/25			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0025372	PMID:26908836	PCS		15/22			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000407	PMID:26908836	PCS		10/24			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000926	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000767	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001537	PMID:1702266;PMID:6813001	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01];HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0004607	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000007	PMID:1702266	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000403	PMID:26908836	PCS		13/25			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0005619	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000768	PMID:26908836	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001538	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001654	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0005616	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002788	PMID:26908836	PCS		18/26			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000324	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000687	PMID:26908836	PCS		13/21			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0003375	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002240	PMID:1702266;PMID:6813001	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01];HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002680	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001270	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0008430	OMIM:253220	TAS					P	HPO:probinson[2012-06-11]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000613	PMID:26908836	PCS		6/20			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001789	PMID:26908836;PMID:9099834	PCS		56/119			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000212	PMID:26908836	PCS		12/21			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000256	PMID:26908836	PCS		26/30			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002159	OMIM:253220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001744	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0006536	PMID:26908836	PCS		11/25			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0006119	OMIM:253220	IEA					P	HPO:iea[2009-02-17]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002650	PMID:26908836	PCS		18/26			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001762	PMID:26908836	PCS		9/26			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0003541	PMID:6813001	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0008818	PMID:6813001	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000470	PMID:26908836	PCS		22/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002808	PMID:6813001;PMID:26908836	PCS		18/26			P	HPO:probinson[2023-07-08];HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0008301	OMIM:253220	TAS					P	HPO:probinson[2012-05-28]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000943	PMID:26908836	PCS		26/29			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0001638	PMID:26908836	PCS		9/24			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0000505	PMID:26908836	PCS		9/24			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0002208	PMID:26908836	PCS		19/31			P	HPO:probinson[2022-02-01]
OMIM:253220	Mucopolysaccharidosis VII		HP:0004469	PMID:26908836	PCS		7/29			P	HPO:probinson[2022-02-01]
OMIM:160120	Episodic ataxia, type 1		HP:0001155	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0002311	OMIM:160120	IEA					P	HPO:skoehler[2018-10-08]
OMIM:160120	Episodic ataxia, type 1		HP:0002411	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0003236	OMIM:160120	TAS					P	HPO:skoehler[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0003621	OMIM:160120	IEA					C	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0003487	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0002321	OMIM:160120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:160120	Episodic ataxia, type 1		HP:0002131	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0003011	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0001260	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0002064	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0001350	OMIM:160120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:160120	Episodic ataxia, type 1		HP:0003828	OMIM:160120	TAS					M	HPO:skoehler[2013-05-31]
OMIM:160120	Episodic ataxia, type 1		HP:0002315	OMIM:160120	TAS					P	HPO:skoehler[2012-10-17]
OMIM:160120	Episodic ataxia, type 1		HP:0000006	OMIM:160120	IEA					I	HPO:iea[2009-02-17]
OMIM:160120	Episodic ataxia, type 1		HP:0001337	OMIM:160120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:160120	Episodic ataxia, type 1		HP:0000622	OMIM:160120	TAS					P	HPO:skoehler[2013-05-31]
OMIM:160120	Episodic ataxia, type 1		HP:0001347	OMIM:160120	IEA					P	HPO:iea[2009-02-17]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0031956	PMID:34585848	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0002240	PMID:34585848	PCS		0/1			P	HPO:probinson[2022-07-11]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0003593	PMID:34585848	PCS		1/1			C	HPO:probinson[2022-07-11]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0000007	PMID:34585848	PCS					I	HPO:probinson[2022-07-11]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0033479	PMID:34585848	PCS		0/1			P	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0000989	PMID:34585848	PCS		0/1			P	HPO:probinson[2022-07-11]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0012202	PMID:34585848	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:619874	Cholestasis, progressive familial intrahepatic, 11		HP:0031964	PMID:34585848	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0009804	PMID:28301459	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0002164	PMID:28301459	PCS		0/3			P	HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0012905	PMID:28301459	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0030001	PMID:28301459	PCS		2/3			P	HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0410030	PMID:28301459	PCS		2/3			P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0012725	OMIM:617681	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0012368	OMIM:617681	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0007651	PMID:28301459	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0000316	OMIM:617681	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0000348	OMIM:617681	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0009743	PMID:28301459	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0000006	PMID:28301459	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0000698	PMID:28301459	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617681	Blepharocheilodontic syndrome 2		HP:0000324	OMIM:617681	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:305700	Sertoli cell-only syndrome		HP:0000771	OMIM:305700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:305700	Sertoli cell-only syndrome		HP:0001475	OMIM:305700	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:305700	Sertoli cell-only syndrome		HP:0034299	OMIM:305700	TAS					P	HPO:probinson[2022-09-05]
OMIM:305700	Sertoli cell-only syndrome		HP:0001417	OMIM:305700	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:305700	Sertoli cell-only syndrome		HP:0001513	OMIM:305700	IEA					P	HPO:iea[2009-02-17]
OMIM:305700	Sertoli cell-only syndrome		HP:0000006	OMIM:305700	TAS					I	HPO:probinson[2022-09-04]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0001265	OMIM:605285	TAS					P	HPO:skoehler[2013-07-30]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0003676	PMID:10915613	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0003621	PMID:10915613;PMID:11601496	PCS		31/31			C	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0002650	OMIM:605285	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0003387	PMID:10915613	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0003431	PMID:10915613	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0001761	PMID:11601496	PCS		19/21			P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0008959	PMID:11601496	PCS		21/21			P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0001288	PMID:10915613	PCS					P	HPO:skoehler[2013-07-30];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0002460	PMID:10915613	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0003450	PMID:10915613	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0001284	PMID:11601496	PCS		21/21			P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0003470	OMIM:605285	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0034337	PMID:10915613	PCS					P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0007182	PMID:10915613	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0009053	PMID:11601496	PCS		21/21			P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0001618	PMID:11601496	PCS		1/21			P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0000508	PMID:11601496	PCS		1/21			P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0009830	PMID:10915613	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0002936	PMID:11601496	PCS		21/21			P	HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0000007	PMID:10915613	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:605285	Neuropathy, hereditary motor and sensory, Russe type		HP:0008944	PMID:11601496	PCS		21/21			P	HPO:probinson[2023-02-12]
OMIM:612921	3-M syndrome 2		HP:0003510	PMID:23457316	PCS		1/1			P	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0000343	PMID:19481195;PMID:27796265	PCS		6/9			P	HPO:probinson[2021-07-07];HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0000684	OMIM:612921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:612921	3-M syndrome 2		HP:0004322	PMID:27796265	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0000463	PMID:23457316;PMID:19481195	PCS		9/9			P	HPO:probinson[2021-07-07];HPO:probinson[2013-04-07]
OMIM:612921	3-M syndrome 2		HP:0003691	PMID:19481195	PCS		2/8			P	HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0002680	PMID:23457316	PCS		1/1			P	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0004482	OMIM:612921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:612921	3-M syndrome 2		HP:0005274	PMID:23457316;PMID:27796265	PCS		2/2			P	HPO:probinson[2021-07-07];HPO:probinson[2013-04-07];HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0012428	PMID:19481195	PCS		8/8			P	HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0010306	OMIM:612921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:612921	3-M syndrome 2		HP:0012471	PMID:23457316;PMID:19481195	PCS		7/9			P	HPO:probinson[2021-07-07];HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0011220	PMID:23457316	PCS		1/1			P	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0002938	PMID:27796265	PCS		1/1			P	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0011461	PMID:27796265	PCS		1/1			C	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0003307	PMID:23457316;PMID:19481195	PCS		8/9			P	HPO:probinson[2021-07-07];HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0000218	OMIM:612921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:612921	3-M syndrome 2		HP:0030084	PMID:23457316	PCS		1/1			P	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0000411	PMID:19481195	PCS		5/8			P	HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0002750	PMID:23457316	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0003100	PMID:23457316;PMID:19481195	PCS		5/9			P	HPO:probinson[2021-07-07];HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0000470	PMID:19481195	PCS		5/8			P	HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0000272	PMID:23457316	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0005280	PMID:23457316	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0001518	PMID:27796265	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0000689	OMIM:612921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:612921	3-M syndrome 2		HP:0000007	OMIM:612921	TAS					I	HPO:probinson[2013-04-07]
OMIM:612921	3-M syndrome 2		HP:0000307	PMID:19481195;PMID:27796265	PCS		8/9			P	HPO:probinson[2021-07-07];HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0009237	OMIM:612921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:612921	3-M syndrome 2		HP:0000768	PMID:23457316	PCS		1/1			P	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0001511	PMID:27796265	PCS		1/1			P	HPO:probinson[2021-07-07]
OMIM:612921	3-M syndrome 2		HP:0002007	PMID:19481195	PCS		8/8			P	HPO:probinson[2013-04-07]
OMIM:612921	3-M syndrome 2		HP:0000268	PMID:19481195	PCS		7/8			P	HPO:probinson[2015-03-21]
OMIM:612921	3-M syndrome 2		HP:0000883	OMIM:612921	IEA					P	HPO:skoehler[2019-02-22]
OMIM:612921	3-M syndrome 2		HP:0000325	PMID:23457316;PMID:19481195;PMID:27796265	PCS		9/10			P	HPO:probinson[2021-07-07];HPO:probinson[2015-03-21]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001298	OMIM:614388	IEA					P	HPO:skoehler[2015-01-27]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0003676	OMIM:614388	TAS					C	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002188	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000486	OMIM:614388	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001250	OMIM:614388	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001252	OMIM:614388;PMID:26992161	PCS		11/11			P	HPO:probinson[2022-08-07];HPO:skoehler[2014-11-26]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001290	OMIM:614388	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001270	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0012169	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001508	OMIM:614388	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0010055	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0007021	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000657	OMIM:614388	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000711	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001522	PMID:17460227	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0003348	PMID:17460227	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0003128	OMIM:614388	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0003623	PMID:26992161;PMID:17460227	PCS		2/2			C	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0008936	PMID:17460227	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002059	OMIM:614388	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000252	PMID:17460227	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002133	OMIM:614388	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0011968	PMID:17460227	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000490	PMID:17460227	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001263	PMID:26992161	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002151	PMID:26992161;PMID:17460227	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001284	PMID:17460227	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002490	PMID:17460227	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0011304	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0034298	PMID:17460227	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0007256	OMIM:614388	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000007	OMIM:614388	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0001558	PMID:17460227	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0200134	OMIM:614388	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000648	OMIM:614388	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000307	PMID:17460227	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002307	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000543	PMID:17460227	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002305	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000006	PMID:17460227	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0000666	PMID:17460227	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614388	Encephalopathy due to defective mitochondrial and peroxisomal fission 1		HP:0002643	PMID:26992161	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:132100	Photoparoxysmal response 1		HP:0010852	OMIM:132100	TAS					P	HPO:probinson[2013-04-05]
OMIM:132100	Photoparoxysmal response 1		HP:0003831	OMIM:132100	TAS					I	HPO:skoehler[2012-10-17]
OMIM:132100	Photoparoxysmal response 1		HP:0000006	OMIM:132100	TAS					I	HPO:probinson[2013-04-05]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0001386	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0001760	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0002751	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0003016	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0004576	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0001387	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0001288	OMIM:208230	TAS					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0002970	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0100490	OMIM:208230	TAS					P	HPO:skoehler[2012-10-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0003040	OMIM:208230	TAS					P	HPO:skoehler[2015-01-21]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0003371	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0003071	OMIM:208230	TAS					P	HPO:probinson[2013-04-08]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0010580	OMIM:208230	TAS					P	HPO:probinson[2013-04-08]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0000939	OMIM:208230	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0006163	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0009473	OMIM:208230	TAS					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0000926	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0000007	OMIM:208230	IEA					I	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0002515	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0002812	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0002758	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0001324	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0004637	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:208230	Arthropathy, progressive pseudorheumatoid, of childhood		HP:0006247	OMIM:208230	IEA					P	HPO:iea[2009-02-17]
OMIM:301200	Amelogenesis imperfecta, type IE		HP:0000705	PMID:15111628	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:301200	Amelogenesis imperfecta, type IE		HP:0009102	PMID:15111628	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-09]
OMIM:301200	Amelogenesis imperfecta, type IE		HP:0006297	PMID:15111628	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-10-09]
OMIM:301200	Amelogenesis imperfecta, type IE		HP:0010299	PMID:15111628	PCS		0/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-10-09]
OMIM:301200	Amelogenesis imperfecta, type IE		HP:0001423	PMID:1916828	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:610688	Joubert syndrome 6		HP:0001320	PMID:17160906	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0003774	OMIM:610688	TAS					P	HPO:skoehler[2012-11-26]
OMIM:610688	Joubert syndrome 6		HP:0002365	PMID:17160906	PCS		2/5			P	HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0002198	PMID:17160906	PCS		1/5			P	HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0001263	PMID:17160906	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0001395	PMID:17160906	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0001252	PMID:17160906	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0001251	PMID:17160906	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0000090	OMIM:610688	TAS					P	HPO:probinson[2012-06-10]
OMIM:610688	Joubert syndrome 6		HP:0011933	OMIM:610688	TAS					P	HPO:probinson[2012-06-10]
OMIM:610688	Joubert syndrome 6		HP:0100951	OMIM:610688	IEA					P	HPO:iea[2009-02-17]
OMIM:610688	Joubert syndrome 6		HP:0001408	PMID:17160906	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0000618	OMIM:610688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610688	Joubert syndrome 6		HP:0000657	PMID:17160906	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0000007	PMID:17160906	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0002419	PMID:17160906	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0000546	OMIM:610688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610688	Joubert syndrome 6		HP:0000733	PMID:17160906	PCS		1/2			P	HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0005957	OMIM:610688	IEA					P	HPO:iea[2009-02-17]
OMIM:610688	Joubert syndrome 6		HP:0002404	PMID:17160906	PCS		2/5			P	HPO:probinson[2012-06-10];HPO:probinson[2022-09-02]
OMIM:610688	Joubert syndrome 6		HP:0000567	OMIM:610688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610688	Joubert syndrome 6		HP:0001249	PMID:17160906	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0002421	PMID:24462369	PCS	HP:0003593	2/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0002169	PMID:24462369	PCS		1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0003236	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0003355	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001250	PMID:25293719;PMID:24462369	PCS		9/11			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0003593	PMID:24462369	PCS		10/10			C	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0010544	PMID:24462369	PCS		1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001290	PMID:24462369	PCS		5/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0003073	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0008151	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001508	PMID:24462369	PCS	HP:0003623				P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0100704	PMID:24462369	PCS		1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001943	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001522	PMID:24462369	PCS		4/10			C	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001942	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0003128	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0000252	PMID:24462369	PCS		1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0002510	PMID:24462369	PCS		1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0002650	PMID:24462369	PCS		2/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0002133	PMID:24462369	PCS		2/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0011968	PMID:24462369	PCS					P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001283	PMID:24462369	PCS		1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0002151	PMID:25293719;PMID:24462369	PCS		11/11			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0002490	PMID:24462369	PCS		10/10			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0011421	PMID:24462369	PCS		1/10			C	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0030746	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0003819	PMID:24462369	PCS		1/10			C	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001518	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0025405	PMID:24462369	PCS					P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0000007	PMID:24462369	PCS					I	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001998	PMID:24462369	PCS	HP:0003623	1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0008347	PMID:24462369	PCS		10/10			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0003811	PMID:25293719	PCS		1/1			C	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001511	PMID:25293719	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0000666	PMID:24462369	PCS		1/10			P	HPO:probinson[2020-12-06]
OMIM:619055	Mitochondrial complex IV deficiency, nuclear type 12		HP:0001336	PMID:24462369	PCS		2/10			P	HPO:probinson[2020-12-06]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0010848	PMID:25477152	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001344	OMIM:616366	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001250	PMID:25477152	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0002373	PMID:25477152	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001252	PMID:25477152	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001263	PMID:25477152	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001251	PMID:25477152	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0003593	OMIM:616366	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0032794	PMID:25477152	PCS	HP:0011463	1/1			P	HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0011463	PMID:25477152	PCS		1/1			C	HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0200134	PMID:25477152	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0000006	PMID:25477152	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001249	OMIM:616366	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001337	OMIM:616366	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616366	Epileptic encephalopathy, early infantile, 32		HP:0001336	OMIM:616366	TAS					P	HPO:skoehler[2015-05-31]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0001397	OMIM:610717	TAS					P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003236	OMIM:610717	TAS					P	HPO:probinson[2013-04-01]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0000365	PMID:17187067	PCS		0/3			P	HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0004322	PMID:17187067	PCS		2/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003198	PMID:17187067	PCS		3/3			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0001252	OMIM:610717	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0002240	PMID:17187067	PCS		2/3			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0002380	OMIM:610717	TAS					P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0001290	OMIM:610717	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003391	OMIM:610717	TAS					P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0000819	PMID:17187067	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0009046	OMIM:610717	TAS					P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003701	PMID:18952067	PCS					P	HPO:probinson[2013-04-01]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0002910	PMID:17187067	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0001744	PMID:17187067	PCS		0/3			P	HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003546	PMID:18952067	PCS					P	HPO:probinson[2013-04-01]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003326	OMIM:610717	TAS					P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0000252	PMID:17187067	PCS		0/3			P	HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0002155	OMIM:610717	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0031936	OMIM:610717	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0001288	OMIM:610717	TAS					P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003388	OMIM:610717	TAS					P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003581	OMIM:610717	TAS					C	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0001284	OMIM:610717	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0006280	PMID:17187067	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0008064	PMID:17187067	PCS		0/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0000407	OMIM:610717	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0009058	PMID:17187067	PCS		3/3			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0000007	PMID:17187067	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0001638	PMID:17187067	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2024-03-14]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0003677	OMIM:610717	TAS					C	HPO:skoehler[2013-10-06]
OMIM:610717	Neutral lipid storage disease with myopathy		HP:0000467	OMIM:610717	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:143100	Huntington disease		HP:0002067	OMIM:143100	IEA					P	HPO:iea[2009-02-17]
OMIM:143100	Huntington disease		HP:0000496	OMIM:143100	IEA					P	HPO:iea[2009-02-17]
OMIM:143100	Huntington disease		HP:0001250	OMIM:143100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:143100	Huntington disease		HP:0001272	OMIM:143100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:143100	Huntington disease		HP:0002066	OMIM:143100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:143100	Huntington disease		HP:0002063	OMIM:143100	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:143100	Huntington disease		HP:0002072	OMIM:143100	IEA					P	HPO:iea[2009-02-17]
OMIM:143100	Huntington disease		HP:0002171	OMIM:143100	TAS					P	HPO:probinson[2009-02-17]
OMIM:143100	Huntington disease		HP:0000716	OMIM:143100	IEA					P	HPO:iea[2009-02-17]
OMIM:143100	Huntington disease		HP:0000726	OMIM:143100	IEA					P	HPO:iea[2009-02-17]
OMIM:143100	Huntington disease		HP:0002529	OMIM:143100	TAS					P	HPO:probinson[2009-02-17]
OMIM:143100	Huntington disease		HP:0000751	OMIM:143100	IEA					P	HPO:iea[2009-02-17]
OMIM:143100	Huntington disease		HP:0000006	OMIM:143100	IEA					I	HPO:iea[2009-02-17]
OMIM:143100	Huntington disease		HP:0001347	OMIM:143100	IEA					P	HPO:iea[2009-02-17]
OMIM:615109	Cowden syndrome 6		HP:0003002	PMID:23246288	PCS		1/2			P	HPO:skoehler[2015-09-25];HPO:probinson[2025-10-03]
OMIM:615109	Cowden syndrome 6		HP:0012740	PMID:23246288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:615109	Cowden syndrome 6		HP:0002890	PMID:23246288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:615109	Cowden syndrome 6		HP:0003581	PMID:23246288	PCS					C	HPO:skoehler[2015-09-25];HPO:probinson[2025-10-03]
OMIM:615109	Cowden syndrome 6		HP:0005584	PMID:23246288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:615109	Cowden syndrome 6		HP:0025388	PMID:23246288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:615109	Cowden syndrome 6		HP:0011462	PMID:23246288	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:615109	Cowden syndrome 6		HP:0000006	PMID:23246288	PCS					I	HPO:skoehler[2015-09-25];HPO:probinson[2020-07-24]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0000819	OMIM:602475	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0000925	OMIM:602475	IEA					P	HPO:iea[2009-02-17]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0002176	OMIM:602475	IEA					P	HPO:iea[2009-02-17]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0011001	OMIM:602475	IEA					P	HPO:iea[2009-02-17]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0002196	OMIM:602475	IEA					P	HPO:iea[2009-02-17]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0011986	OMIM:602475	IEA					P	HPO:skoehler[2019-09-07]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0000007	OMIM:602475	IEA					I	HPO:iea[2009-02-17]
OMIM:602475	Ossification of the posterior longitudinal ligament of spine		HP:0001347	OMIM:602475	IEA					P	HPO:iea[2009-02-17]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0001355	PMID:21624973	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0001250	PMID:21624973	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0007341	OMIM:604004	IEA					P	HPO:iea[2009-02-17]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0001251	OMIM:604004	IEA					P	HPO:iea[2009-02-17]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0003593	PMID:21624973	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0000007	PMID:11254442	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0001270	OMIM:604004	IEA					P	HPO:iea[2009-02-17]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0001257	OMIM:604004	IEA					P	HPO:iea[2009-02-17]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0000256	PMID:21624973	PCS	HP:0003593	1/1			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-01-30]
OMIM:604004	Megalencephalic leukoencephalopathy with subcortical cysts 1		HP:0006943	OMIM:604004	IEA					P	HPO:iea[2009-02-17]
OMIM:147400	Incisors, shovel-shaped		HP:0010982	OMIM:147400	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:147400	Incisors, shovel-shaped		HP:0006358	OMIM:147400	IEA					P	HPO:iea[2009-02-17]
OMIM:147400	Incisors, shovel-shaped		HP:0000006	OMIM:147400	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003236	PMID:34048612	PCS		9/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003596	PMID:34048612	PCS		10/11			C	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003691	PMID:34048612	PCS		10/10			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0002380	PMID:34048612	PCS		3/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0033685	PMID:34048612	PCS					P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0012548	PMID:34048612	PCS					P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0030319	PMID:34048612	PCS		3/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0100297	PMID:34048612	PCS					P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0100543	PMID:34048612	PCS		3/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0009023	PMID:34048612	PCS		11/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0034045	PMID:34048612	PCS					P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003805	PMID:34048612	PCS					P	HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0025710	PMID:34048612	PCS		1/11			C	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0001265	PMID:34048612	PCS		2/10			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0030007	PMID:34048612	PCS		4/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003687	PMID:34048612	PCS					P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003487	PMID:34048612	PCS		1/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0001260	PMID:34048612	PCS		5/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0001284	PMID:34048612	PCS		6/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0000508	PMID:34048612	PCS		4/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003419	PMID:34048612	PCS		9/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0002307	PMID:34048612	PCS		2/11			P	HPO:probinson[2022-04-11]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0000006	PMID:34048612	PCS					I	HPO:probinson[2022-04-10]
OMIM:619733	Inclusion body myopathy and brain white matter abnormalities		HP:0003557	PMID:34048612	PCS					P	HPO:probinson[2022-04-11]
OMIM:616400	Palmoplantar keratoderma, nonepidermolytic, focal 2		HP:0005588	PMID:25285920	PCS		2/2			P	HPO:probinson[2023-01-20]
OMIM:616400	Palmoplantar keratoderma, nonepidermolytic, focal 2		HP:0000006	PMID:25285920	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000286	PMID:33824347	PCS		2/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0011939	PMID:33824347	PCS		1/5			P	HPO:probinson[2024-07-22]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0006429	PMID:33824347	PCS		5/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000365	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000343	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000486	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000463	PMID:33824347	PCS		2/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0004322	PMID:33824347	PCS		5/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0002684	PMID:33824347	PCS		5/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0100252	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000280	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0011499	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0100255	PMID:33824347	PCS		4/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0100865	PMID:33824347	PCS		5/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0001629	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0100704	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0011220	PMID:33824347	PCS		3/3			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000316	PMID:33824347	PCS		4/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000256	PMID:33824347	PCS		4/10			P	HP:probinson[2022-03-09];HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000179	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000215	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0002753	PMID:33824347	PCS		4/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0003621	PMID:33824347	PCS		1/5			C	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0002694	PMID:33824347	PCS		4/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0004279	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000431	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000771	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0002057	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0007807	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0001263	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0030320	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0410280	PMID:33824347	PCS		4/5			C	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000926	PMID:33824347	PCS		5/5		HP:0012825	P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000007	PMID:33824347	PCS					I	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000667	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000648	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000505	PMID:33824347	PCS	HP:0003621	5/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000268	PMID:33824347	PCS		4/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000520	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0000885	PMID:33824347	PCS		5/5			P	HPO:probinson[2022-03-09]
OMIM:619727	Craniotubular dysplasia, Ikegawa type		HP:0001138	PMID:33824347	PCS		1/5			P	HP:probinson[2022-03-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0003565	PMID:25894502	PCS					P	HPO:skoehler[2015-07-05];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0032979	PMID:32309005	PCS		1/1			P	HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0003493	PMID:25894502	PCS		7/9			P	HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0002094	PMID:25894502	PCS		1/9			P	HPO:skoehler[2015-07-05];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0012735	PMID:25894502	PCS		2/9			P	HPO:skoehler[2015-07-05];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0002091	PMID:25894502	PCS		8/8			P	HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0045051	PMID:25894502	PCS					P	HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0011227	PMID:25894502	PCS					P	HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0040223	PMID:25894502	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0012574	PMID:25894502	PCS		1/4			P	HPO:probinson[2020-06-09];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0002829	PMID:25894502	PCS	HP:0011463	5/21			P	HPO:skoehler[2015-07-05];HPO:probinson[2020-06-09];HPO:probinson[2021-02-13]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0011463	PMID:25894502	PCS		16/21			C	HPO:probinson[2021-02-13]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0008653	PMID:25894502	PCS		2/4			P	HPO:skoehler[2015-07-05];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0006530	PMID:25894502	PCS		9/9			P	HPO:skoehler[2015-07-05];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0002789	PMID:25894502	PCS		2/9			P	HPO:skoehler[2015-07-05];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0000006	PMID:25894502	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-06-09]
OMIM:616414	Autoimmune interstitial lung, joint, and kidney disease		HP:0001369	PMID:25894502	PCS		20/21			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-06-09];HPO:probinson[2021-02-13]
OMIM:274700	Thyroid hormonogenesis, genetic defect in, 3		HP:0002890	OMIM:274700	TAS					P	HPO:skoehler[2010-06-18]
OMIM:274700	Thyroid hormonogenesis, genetic defect in, 3		HP:0000007	OMIM:274700	TAS					I	HPO:skoehler[2009-02-17]
OMIM:274700	Thyroid hormonogenesis, genetic defect in, 3		HP:0008223	OMIM:274700	TAS					P	HPO:skoehler[2010-06-20]
OMIM:274700	Thyroid hormonogenesis, genetic defect in, 3		HP:0012559	OMIM:274700	TAS					P	HPO:probinson[2014-01-04]
OMIM:274700	Thyroid hormonogenesis, genetic defect in, 3		HP:0000853	OMIM:274700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:274700	Thyroid hormonogenesis, genetic defect in, 3		HP:0001249	OMIM:274700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:614203	Parkinson disease 17		HP:0002322	OMIM:614203	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614203	Parkinson disease 17		HP:0002067	OMIM:614203	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614203	Parkinson disease 17		HP:0001300	OMIM:614203	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614203	Parkinson disease 17		HP:0002063	OMIM:614203	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614203	Parkinson disease 17		HP:0003581	PMID:21763482	PCS					C	HPO:probinson[2023-05-13]
OMIM:614203	Parkinson disease 17		HP:0002172	OMIM:614203	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614203	Parkinson disease 17		HP:0002304	OMIM:614203	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614203	Parkinson disease 17		HP:0000006	PMID:21763482	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-13]
OMIM:614203	Parkinson disease 17		HP:0001337	OMIM:614203	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614203	Parkinson disease 17		HP:0100660	OMIM:614203	TAS					P	HPO:skoehler[2013-05-31]
OMIM:614565	Night blindness, congenital stationary, type 1E		HP:0000486	PMID:22325361	PCS		2/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-22]
OMIM:614565	Night blindness, congenital stationary, type 1E		HP:0000639	PMID:22325361	PCS		4/7		HP:0012826	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-22]
OMIM:614565	Night blindness, congenital stationary, type 1E		HP:0000007	PMID:22325361	PCS					I	HPO:skoehler[2013-10-22];HPO:probinson[2023-02-22]
OMIM:614565	Night blindness, congenital stationary, type 1E		HP:0007663	PMID:22325361	PCS		2/7			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-22]
OMIM:614565	Night blindness, congenital stationary, type 1E		HP:0007642	PMID:22325361	PCS		7/7			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-22]
OMIM:614565	Night blindness, congenital stationary, type 1E		HP:0000505	PMID:22325361	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:614565	Night blindness, congenital stationary, type 1E		HP:0011003	PMID:22325361	PCS		2/7			P	HPO:probinson[2023-02-22]
OMIM:270200	Sjogren-Larsson syndrome		HP:0001595	PMID:6179662	PCS		0/36			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:270200	Sjogren-Larsson syndrome		HP:0003577	PMID:6179662;PMID:11124298	PCS		51/51			C	HPO:probinson[2022-04-30];HPO:probinson[2024-03-09]
OMIM:270200	Sjogren-Larsson syndrome		HP:0000483	PMID:11124298	PCS		10/15			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0001597	PMID:6179662	PCS		0/36			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:270200	Sjogren-Larsson syndrome		HP:0004322	OMIM:270200	TAS					P	HPO:probinson[2009-02-17]
OMIM:270200	Sjogren-Larsson syndrome		HP:0001250	OMIM:270200	TAS					P	HPO:probinson[2009-02-17]
OMIM:270200	Sjogren-Larsson syndrome		HP:0001371	PMID:16476818	PCS		6/6			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0006297	OMIM:270200	TAS					P	HPO:probinson[2009-02-17]
OMIM:270200	Sjogren-Larsson syndrome		HP:0000613	PMID:25784589;PMID:11124298	PCS		22/24			P	HPO:probinson[2022-04-30];HPO:probinson[2012-07-17];HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0007663	PMID:16476818;PMID:11124298	PCS		19/19			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0007722	PMID:25784589	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0007305	OMIM:270200	TAS					P	HPO:probinson[2009-02-17]
OMIM:270200	Sjogren-Larsson syndrome		HP:0001249	PMID:8528251	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:270200	Sjogren-Larsson syndrome		HP:0002313	PMID:16476818	PCS		6/6			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0030501	PMID:25784589	IEA		9/9			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0007727	OMIM:270200	TAS					P	HPO:probinson[2009-02-17]
OMIM:270200	Sjogren-Larsson syndrome		HP:0000551	PMID:16476818	PCS		3/6			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0031717	PMID:11124298	PCS		2/15			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:6000720	PMID:1939650	PCS		7/7			P	HPO:probinson[2024-06-29]
OMIM:270200	Sjogren-Larsson syndrome		HP:0032028	PMID:16476818;PMID:11124298	PCS		20/21			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0030329	OMIM:270200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270200	Sjogren-Larsson syndrome		HP:0008064	PMID:25784589	PCS		9/9			P	HPO:probinson[2012-07-17];HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0008064	PMID:16476818	PCS		6/6			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0008064	PMID:11124298	PCS	HP:0003577	15/15			P	HPO:probinson[2022-04-30]
OMIM:270200	Sjogren-Larsson syndrome		HP:0008064	PMID:8528251	PCS		3/3			P	HPO:probinson[2024-03-09]
OMIM:270200	Sjogren-Larsson syndrome		HP:0008064	PMID:6179662	PCS		36/36			P	HPO:probinson[2024-03-09]
OMIM:270200	Sjogren-Larsson syndrome		HP:0000608	OMIM:270200	TAS					P	HPO:probinson[2012-07-17]
OMIM:270200	Sjogren-Larsson syndrome		HP:0000007	PMID:8528251	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:270200	Sjogren-Larsson syndrome		HP:0002942	OMIM:270200	TAS					P	HPO:probinson[2009-02-17]
OMIM:270200	Sjogren-Larsson syndrome		HP:0001257	PMID:25784589;PMID:8528251	PCS		12/12			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-30];HPO:probinson[2024-03-09]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0001903	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0011463	PMID:28487541	PCS		3/3			C	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0004808	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0005518	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0005528	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0001873	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0000006	PMID:28487541	PCS					I	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0001876	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0031689	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0002863	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:619041	Monosomy 7 myelodysplasia and leukemia syndrome 2		HP:0001875	PMID:28487541	PCS					P	HPO:probinson[2021-01-30]
OMIM:620818	MHC class II deficiency 5		HP:0002850	PMID:7990905	PCS					P	HPO:probinson[2024-12-14]
OMIM:620818	MHC class II deficiency 5		HP:0031390	PMID:7990905	PCS					P	HPO:probinson[2024-12-14]
OMIM:620818	MHC class II deficiency 5		HP:0002373	PMID:7990905	PCS	HP:0003593	1/2			P	HPO:probinson[2024-12-14]
OMIM:620818	MHC class II deficiency 5		HP:0003593	PMID:7990905	PCS		2/2			C	HPO:probinson[2024-12-14]
OMIM:620818	MHC class II deficiency 5		HP:0000007	OMIM:620818	TAS					I	HPO:probinson[2024-12-14]
OMIM:620818	MHC class II deficiency 5		HP:0002090	PMID:7990905	PCS		1/2			P	HPO:probinson[2024-12-14]
OMIM:620818	MHC class II deficiency 5		HP:0002720	PMID:7990905	PCS					P	HPO:probinson[2024-12-14]
OMIM:620818	MHC class II deficiency 5		HP:0004315	PMID:7990905	PCS					P	HPO:probinson[2024-12-14]
OMIM:182990	Spinal intradural arachnoid cysts		HP:0000925	OMIM:182990	IEA					P	HPO:iea[2009-02-17]
OMIM:182990	Spinal intradural arachnoid cysts		HP:0010550	OMIM:182990	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182990	Spinal intradural arachnoid cysts		HP:0100702	OMIM:182990	IEA					P	HPO:skoehler[2015-01-27]
OMIM:182990	Spinal intradural arachnoid cysts		HP:0000006	OMIM:182990	IEA					I	HPO:iea[2009-02-17]
OMIM:600510	Glaucoma-Related pigment dispersion syndrome		HP:0011462	OMIM:600510	TAS					C	HPO:probinson[2013-12-21]
OMIM:600510	Glaucoma-Related pigment dispersion syndrome		HP:0012108	OMIM:600510	TAS					P	HPO:probinson[2013-12-21]
OMIM:600510	Glaucoma-Related pigment dispersion syndrome		HP:0000648	OMIM:600510	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600510	Glaucoma-Related pigment dispersion syndrome		HP:0000545	OMIM:600510	TAS					P	HPO:skoehler[2010-06-20]
OMIM:600510	Glaucoma-Related pigment dispersion syndrome		HP:0000006	OMIM:600510	TAS					I	HPO:skoehler[2015-12-30]
OMIM:601626	Leukemia, acute myeloid		HP:0001442	OMIM:601626	TAS					I	HPO:skoehler[2019-02-22]
OMIM:601626	Leukemia, acute myeloid		HP:0004808	OMIM:601626	TAS					P	HPO:skoehler[2010-06-20]
OMIM:601626	Leukemia, acute myeloid		HP:0000006	OMIM:601626	TAS					I	HPO:skoehler[2009-02-17]
OMIM:620830	Auroneurodental syndrome		HP:0000286	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000160	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0002066	PMID:34805998	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0002162	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0001252	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0003593	PMID:34805998	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0012450	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000316	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000219	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000411	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0003701	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0003327	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000278	PMID:34805998	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000699	PMID:34805998	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0002553	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0006956	PMID:34805998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0025372	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0011968	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0001263	PMID:34805998	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0001182	PMID:34805998	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0012378	PMID:34805998	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0010535	PMID:34805998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0034295	PMID:34805998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000407	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000508	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0006342	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000007	PMID:34805998	PCS					I	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0100716	PMID:34805998	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:620830	Auroneurodental syndrome		HP:0000369	PMID:34805998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-23]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0003577	PMID:27259054	PCS		5/5			C	HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0000750	PMID:27259054	PCS		5/5			P	HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001344	PMID:27259054	PCS		2/5			P	HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0000486	PMID:27259054	PCS		1/5			P	HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001263	PMID:27259054	PCS		5/5			P	HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001252	PMID:27259054	PCS		3/5			P	HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001629	PMID:27259054	PCS	HP:0003577	4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0000519	PMID:27259054	PCS		2/5			P	HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0000007	PMID:27259054	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0000733	PMID:27259054	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0000722	PMID:27259054	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0003508	PMID:27259054	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0100716	PMID:27259054	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001643	PMID:27259054	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0000554	PMID:27259054	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001631	PMID:27259054	PCS	HP:0003577	2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0007018	PMID:27259054	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001249	PMID:27259054	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:617044	Short stature, developmental delay, and congenital heart defects		HP:0001655	PMID:27259054	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-09]
OMIM:275350	Transcobalamin II deficiency		HP:0001254	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0001252	PMID:7849710;PMID:19373259	PCS		2/4			P	HPO:probinson[2024-03-16];HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0003593	PMID:7849710;PMID:19373259	PCS		3/4			C	HPO:probinson[2024-03-16];HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0002240	PMID:7849710	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0001251	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0002160	PMID:19373259	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:275350	Transcobalamin II deficiency		HP:0012133	PMID:7849710	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0001508	PMID:7849710;PMID:19373259	PCS		4/4			P	HPO:probinson[2024-03-16];HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0000737	PMID:7849710	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0001903	PMID:19373259	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:275350	Transcobalamin II deficiency		HP:0001324	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0001249	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0003623	PMID:19373259	PCS		1/3			C	HPO:probinson[2024-03-16]
OMIM:275350	Transcobalamin II deficiency		HP:0004315	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0001980	PMID:7849710	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0002014	OMIM:275350	IEA		1/3			P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0002850	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0002013	OMIM:275350	IEA		2/3			P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0040126	PMID:19373259	PCS		0/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-16]
OMIM:275350	Transcobalamin II deficiency		HP:0040087	PMID:7849710	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0012120	PMID:7849710;PMID:19373259	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05];HPO:probinson[2024-03-16]
OMIM:275350	Transcobalamin II deficiency		HP:0000007	PMID:7849710	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0001896	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0001972	PMID:7849710	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:275350	Transcobalamin II deficiency		HP:0001876	OMIM:275350	IEA		2/3			P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0002720	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:275350	Transcobalamin II deficiency		HP:0001875	OMIM:275350	IEA					P	HPO:iea[2009-02-17]
OMIM:119540	Cleft palate, isolated		HP:0000175	OMIM:119540	TAS					P	HPO:skoehler[2009-02-17]
OMIM:119540	Cleft palate, isolated		HP:0011094	OMIM:119540	TAS					P	HPO:skoehler[2012-11-16]
OMIM:119540	Cleft palate, isolated		HP:0001250	OMIM:119540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:119540	Cleft palate, isolated		HP:0009102	OMIM:119540	TAS					P	HPO:skoehler[2012-07-26]
OMIM:119540	Cleft palate, isolated		HP:0000212	OMIM:119540	TAS					P	HPO:skoehler[2012-07-26]
OMIM:119540	Cleft palate, isolated		HP:0000006	OMIM:119540	IEA					I	HPO:iea[2009-02-17]
OMIM:119540	Cleft palate, isolated		HP:0000347	OMIM:119540	TAS					P	HPO:skoehler[2012-07-26]
OMIM:615135	Maple syrup urine disease, mild variant		HP:0010913	PMID:23086801	PCS	HP:0003623	1/1			P	HPO:probinson[2022-10-02]
OMIM:615135	Maple syrup urine disease, mild variant		HP:0000007	PMID:23086801	PCS					I	HPO:probinson[2022-10-02]
OMIM:615135	Maple syrup urine disease, mild variant		HP:0010911	PMID:23086801	PCS	HP:0003623	1/1			P	HPO:probinson[2022-10-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000286	PMID:20685673	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000582	OMIM:613544	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0003577	PMID:3351912;PMID:20685673	PCS		5/5			C	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000343	PMID:20685673	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0004322	OMIM:613544	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000023	PMID:20685673	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0003196	OMIM:613544	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001252	PMID:20685673	PCS		4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000319	PMID:3351912;PMID:20685673	PCS		5/5			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000954	OMIM:613544	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000316	OMIM:613544	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000219	PMID:3351912;PMID:20685673	PCS		5/5			P	HPO:probinson[2022-11-02];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000218	PMID:20685673;PMID:3351912	PCS		3/3			P	HPO:probinson[2022-11-02];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0003745	OMIM:613544	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000455	OMIM:613544	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001763	PMID:3351912	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001620	PMID:20685673	PCS		1/4			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000252	PMID:20685673	PCS		0/4			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001762	PMID:20685673	PCS		1/4			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001761	PMID:20685673	PCS		1/4			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0011968	PMID:3351912	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001382	PMID:20685673	PCS		4/4			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001263	PMID:3351912;PMID:20685673	PCS		5/5			P	HPO:probinson[2022-11-02];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000470	PMID:3351912	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000294	PMID:20685673	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0011451	PMID:3351912	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0001537	PMID:3351912;PMID:20685673	PCS		2/5			P	HPO:probinson[2022-11-02];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000426	PMID:20685673	PCS		2/2			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000601	OMIM:613544	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0008689	PMID:3351912	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000960	PMID:20685673	PCS		2/4			P	HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000369	PMID:20685673	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613544	Chromosome 6q11-q14 deletion syndrome		HP:0000347	PMID:3351912	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0003521	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001377	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0006429	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0004279	OMIM:271650	TAS					P	HPO:probinson[2013-04-07]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002651	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001241	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0010049	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0004590	OMIM:271650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0100255	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0010743	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002829	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000926	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002938	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000007	OMIM:271650	IEA					I	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000920	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002515	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002812	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000768	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001769	OMIM:271650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002758	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002857	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001169	OMIM:271650	TAS					P	HPO:probinson[2013-04-07]
OMIM:271650	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0009824	OMIM:271650	IEA					P	HPO:iea[2009-02-17]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0003774	PMID:32827185	PCS	HP:0011462	3/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0007737	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0008619	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000750	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000365	PMID:32827185	PCS		4/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0004322	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0003076	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000518	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0011463	PMID:32827185	PCS		6/6			C	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000407	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0002748	PMID:32827185	PCS		4/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000007	PMID:32827185	PCS					I	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000648	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0007994	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000505	PMID:32827185	PCS		6/6			P	HPO:probinson[2022-05-30];HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0002757	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000543	PMID:32827185	PCS		1/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0000510	PMID:32827185	PCS		6/6			P	HPO:probinson[2022-05-30]
OMIM:268315	Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction		HP:0001994	PMID:32827185	PCS		6/6			P	HPO:probinson[2022-05-30]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000483	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000365	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001212	OMIM:135900	IEA					P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000486	PMID:22405089	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000089	OMIM:135900	TAS					P	HPO:probinson[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0004322	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000086	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000639	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001609	OMIM:135900	IEA					P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000998	PMID:22405089	PCS		2/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0008897	OMIM:135900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000879	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0006237	OMIM:135900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000358	OMIM:135900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:135900	Coffin-Siris syndrome 1		HP:0009747	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000494	PMID:22405089	PCS		4/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000252	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002673	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0003083	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001338	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000527	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0004209	PMID:22405089	PCS		2/9			P	HPO:probinson[2021-06-21];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0006863	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001852	PMID:22405089	PCS		2/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000006	PMID:22405089	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000369	OMIM:135900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000248	PMID:22405089	PCS		2/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000126	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000343	PMID:22405089	PCS		1/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0100391	OMIM:135900	TAS					P	HPO:probinson[2012-06-10]
OMIM:135900	Coffin-Siris syndrome 1		HP:0003298	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0011359	PMID:22405089	PCS		1/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001305	OMIM:135900	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0008872	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000219	PMID:22405089	PCS		6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000218	PMID:22405089	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000455	PMID:22405089	PCS		6/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000179	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001028	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000698	PMID:22405089	PCS		2/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002650	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000750	PMID:22405089	PCS		9/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000072	PMID:22405089	PCS		1/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002808	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000508	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000505	OMIM:135900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002007	PMID:22405089	PCS		3/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001798	OMIM:135900	IEA					P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000684	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002188	PMID:22405089	PCS		1/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001250	PMID:22405089	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002066	PMID:22405089	PCS		1/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001252	PMID:22405089	PCS		7/9			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000280	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000718	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000954	PMID:22405089	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000316	PMID:22405089	IEA		1/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002219	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001643	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000278	PMID:22405089	PCS		4/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001249	OMIM:135900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000175	PMID:22405089	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000453	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000574	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002750	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002079	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000331	OMIM:135900	IEA					P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001382	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001263	PMID:22405089	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000691	PMID:22405089	PCS		4/8			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002592	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000729	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000965	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001537	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000601	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000722	OMIM:135900	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000047	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000960	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000322	OMIM:135900	IEA					P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002588	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000384	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000023	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001629	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0008398	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0006498	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000377	OMIM:135900	IEA					P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001620	OMIM:135900	IEA					P	HPO:skoehler[2019-09-07]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000776	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000154	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002576	OMIM:135900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:135900	Coffin-Siris syndrome 1		HP:0031936	PMID:22405089	PCS		8/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000151	OMIM:135900	TAS					P	HPO:probinson[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0005280	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0010185	OMIM:135900	TAS					P	HPO:probinson[2012-06-08]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002209	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001636	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0008665	PMID:22405089	PCS		1/5			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001511	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002205	PMID:22405089	PCS		1/9			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001357	PMID:22405089	PCS		2/9			P	HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0001631	PMID:22405089	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000028	PMID:22405089	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0002566	OMIM:135900	IEA					P	HPO:iea[2009-02-17]
OMIM:135900	Coffin-Siris syndrome 1		HP:0000545	PMID:22405089	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-21]
OMIM:135900	Coffin-Siris syndrome 1		HP:0004227	OMIM:135900	TAS					P	HPO:probinson[2012-06-10]
OMIM:613550	Nephronophthisis 11		HP:0003774	PMID:19508969	PCS	HP:0003621	7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000486	PMID:19508969	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0009916	PMID:19508969	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0001395	PMID:19508969	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0001263	PMID:19508969	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0005583	PMID:19508969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000090	PMID:19508969	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000092	PMID:19508969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0001959	PMID:19508969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000639	PMID:19508969	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0001903	PMID:19508969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000007	PMID:19508969	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000546	PMID:19508969	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000108	PMID:19508969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0000103	PMID:19508969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:613550	Nephronophthisis 11		HP:0001510	PMID:19508969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:609508	Stickler sydrome, type I, nonsyndromic ocular		HP:0000365	PMID:12939326	PCS		4/28			P	HPO:probinson[2021-05-02]
OMIM:609508	Stickler sydrome, type I, nonsyndromic ocular		HP:0030663	PMID:15671297	PCS					P	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:609508	Stickler sydrome, type I, nonsyndromic ocular		HP:0012230	PMID:12939326;PMID:15671297	PCS		26/38			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-02]
OMIM:609508	Stickler sydrome, type I, nonsyndromic ocular		HP:0011800	PMID:12939326	PCS		3/28			P	HPO:probinson[2021-05-02]
OMIM:609508	Stickler sydrome, type I, nonsyndromic ocular		HP:0000006	PMID:17721977	PCS					I	HPO:probinson[2013-01-09]
OMIM:609508	Stickler sydrome, type I, nonsyndromic ocular		HP:0000545	PMID:15671297	PCS					P	HPO:probinson[2013-03-30]
OMIM:616428	Microphthalmia, isolated, with coloboma 10		HP:0000528	PMID:25910211	PCS		4/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-05]
OMIM:616428	Microphthalmia, isolated, with coloboma 10		HP:0000612	PMID:25910211	PCS		8/15			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-05]
OMIM:616428	Microphthalmia, isolated, with coloboma 10		HP:0000568	PMID:25910211	PCS		8/15			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-05]
OMIM:616428	Microphthalmia, isolated, with coloboma 10		HP:0034567	PMID:25910211	PCS		1/15			P	HPO:probinson[2023-03-31]
OMIM:616428	Microphthalmia, isolated, with coloboma 10		HP:0025492	PMID:25910211	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-05]
OMIM:616428	Microphthalmia, isolated, with coloboma 10		HP:0000006	PMID:25910211	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:616428	Microphthalmia, isolated, with coloboma 10		HP:0000567	PMID:25910211	PCS		2/15			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-05]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0003621	PMID:15466643	PCS		3/8			C	HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0001297	PMID:15466643	PCS		6/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0025478	OMIM:601154	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0005110	PMID:15466643	PCS		10/21			P	HPO:skoehler[2013-04-18];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0011712	PMID:15466643	PCS		2/21			P	HPO:skoehler[2013-04-18];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0011713	PMID:15466643	PCS		1/21			P	HPO:skoehler[2013-04-18];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0012664	PMID:15466643	PCS		20/21			P	HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0011462	PMID:15466643	PCS		5/8			C	HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0006682	PMID:15466643	PCS		1/21			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0006673	PMID:15466643	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0004749	OMIM:601154	TAS					P	HPO:skoehler[2013-04-18]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0001962	OMIM:601154	TAS					P	HPO:skoehler[2013-04-18]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0006699	OMIM:601154	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0001279	OMIM:601154	TAS					P	HPO:skoehler[2013-04-18]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0001678	OMIM:601154	TAS					P	HPO:skoehler[2013-04-18]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0000006	PMID:15466643	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0001644	PMID:15466643	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:601154	Cardiomyopathy, dilated, 1E		HP:0004755	PMID:15466643	PCS		1/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:235760	Hirschsprung disease with hypoplastic nails and dysmorphic facialfeatures		HP:0001792	OMIM:235760	IEA					P	HPO:iea[2009-02-17]
OMIM:235760	Hirschsprung disease with hypoplastic nails and dysmorphic facialfeatures		HP:0002023	OMIM:235760	IEA					P	HPO:iea[2009-02-17]
OMIM:235760	Hirschsprung disease with hypoplastic nails and dysmorphic facialfeatures		HP:0000023	OMIM:235760	IEA					P	HPO:iea[2009-02-17]
OMIM:235760	Hirschsprung disease with hypoplastic nails and dysmorphic facialfeatures		HP:0002251	OMIM:235760	IEA					P	HPO:iea[2009-02-17]
OMIM:235760	Hirschsprung disease with hypoplastic nails and dysmorphic facialfeatures		HP:0001999	OMIM:235760	IEA				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:235760	Hirschsprung disease with hypoplastic nails and dysmorphic facialfeatures		HP:0000007	OMIM:235760	IEA					I	HPO:iea[2009-02-17]
OMIM:235760	Hirschsprung disease with hypoplastic nails and dysmorphic facialfeatures		HP:0000126	OMIM:235760	IEA					P	HPO:iea[2009-02-17]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002069	PMID:26744459	PCS	HP:0011463	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002421	PMID:26744459	PCS		1/1			P	HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002188	PMID:26744459	PCS		1/1			P	HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0001332	PMID:26744459	PCS	HP:0003623	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002240	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0001290	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000639	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000319	PMID:26744459	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0011166	PMID:26744459	PCS	HP:0011463	1/1			P	HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0006530	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0001107	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000278	PMID:26744459	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0001744	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0008936	PMID:26744459	PCS	HP:0003593	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0001022	PMID:26744459	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002059	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000252	PMID:26744459	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002353	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0011968	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0011344	PMID:26744459	PCS		1/1			P	HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000007	PMID:26744459	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000601	PMID:26744459	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000400	PMID:26744459	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002205	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0000369	PMID:26744459	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002104	PMID:26744459	PCS	HP:0003623	1/1			P	HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0002721	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617050	Hermansky-Pudlak syndrome 10		HP:0001875	PMID:26744459	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000365	PMID:29878199	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0003498	PMID:29878199	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000023	PMID:29878199	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0005257	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0004322	PMID:29878199	PCS		5/5			P	HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0003273	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0003071	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0010585	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0010306	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0100864	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0006297	PMID:29878199	PCS		5/5			P	HPO:probinson[2023-01-21];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0003307	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0002857	PMID:29878199	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000218	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0001763	OMIM:618363	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000311	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0004976	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0003301	PMID:29878199	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0002751	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0003026	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000670	PMID:29878199	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000175	PMID:29878199	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0009804	OMIM:618363	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0002650	PMID:29878199	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0002673	PMID:29878199	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0004233	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0001382	PMID:29878199	PCS		2/5			P	HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0001263	OMIM:618363	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000705	PMID:29878199	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000308	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000007	PMID:29878199	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0003417	PMID:29878199	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0001956	OMIM:618363	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0005616	OMIM:618363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000201	OMIM:618363	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000347	PMID:29878199;OMIM:618363	PCS		12/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0001513	OMIM:618363	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618363	Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis		HP:0000303	PMID:29878199	PCS		1/4			P	HPO:probinson[2023-01-21]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0004325	PMID:22405087	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0002069	PMID:22405087	PCS		6/8			P	HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000486	PMID:22405087	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0001272	PMID:22405087	PCS		3/8			P	HPO:skoehler[2012-11-20];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0002120	PMID:22405087	PCS		6/8			P	HPO:skoehler[2012-11-20];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0001252	PMID:22405087	PCS	HP:0003593	7/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0001251	PMID:22405087	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0003593	PMID:22405087	PCS		8/8			C	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0001508	PMID:22405087	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000639	PMID:22405087	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000556	PMID:22405087	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0007108	PMID:22405087	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0001265	PMID:22405087	PCS		1/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000253	PMID:22405087	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000252	PMID:22405087	PCS		4/8			P	HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0002079	PMID:22405087	PCS		3/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0001284	PMID:22405087	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0011344	PMID:22405087	PCS		8/8			P	HPO:skoehler[2012-11-20];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000407	PMID:22405087	PCS		2/8			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000007	PMID:22405087	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0000648	PMID:22405087	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0002305	PMID:22405087	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0007359	PMID:22405087	PCS		4/8			P	HPO:probinson[2021-06-25]
OMIM:614559	Infantile cerebellar-retinal degeneration		HP:0002500	PMID:22405087	PCS		4/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-25]
OMIM:267740	Retinal degeneration and epilepsy		HP:0001250	OMIM:267740	IEA					P	HPO:iea[2009-02-17]
OMIM:267740	Retinal degeneration and epilepsy		HP:0000007	OMIM:267740	IEA					I	HPO:iea[2009-02-17]
OMIM:267740	Retinal degeneration and epilepsy		HP:0000546	OMIM:267740	IEA					P	HPO:iea[2009-02-17]
OMIM:173000	Pilonidal sinus		HP:0010769	OMIM:173000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:173000	Pilonidal sinus		HP:0000006	OMIM:173000	IEA					I	HPO:iea[2009-02-17]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000175	PMID:19261599	PCS		1/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000494	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0010804	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000475	PMID:19261599	PCS					P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000431	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0001371	PMID:19261599	PCS	HP:0011461	2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0001252	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0002093	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000316	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000007	PMID:19261599	PCS					I	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0001558	PMID:19261599	IEA	HP:0011461	2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0008872	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0001989	PMID:19261599	PCS					P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000218	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000347	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000369	PMID:19261599	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0000028	PMID:19261599	PCS		1/1	MALE		P	HPO:probinson[2020-07-14]
OMIM:618388	Fetal akinesia deformation sequence 2		HP:0001612	PMID:19261599	PCS		1/2			P	HPO:probinson[2020-07-14]
OMIM:619096	Mismatch repair cancer syndrome 2		HP:0003003	PMID:16372347	PCS					P	HPO:probinson[2021-01-01]
OMIM:619096	Mismatch repair cancer syndrome 2		HP:0006727	PMID:11809679	IEA					P	HPO:probinson[2021-01-01]
OMIM:619096	Mismatch repair cancer syndrome 2		HP:0012174	PMID:12549480	PCS					P	HPO:probinson[2021-01-01]
OMIM:619096	Mismatch repair cancer syndrome 2		HP:0000007	PMID:16372347	PCS					I	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619096	Mismatch repair cancer syndrome 2		HP:0007565	PMID:11809679	PCS					P	HPO:probinson[2021-01-01]
OMIM:609285	Congenital myopathy 23		HP:0001276	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0003577	PMID:11738357;PMID:23378224	PCS		4/9			C	ORCID:0000-0002-0736-9199[2024-06-29];HPO:probinson[2022-08-06]
OMIM:609285	Congenital myopathy 23		HP:0003236	PMID:23378224	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0003555	PMID:23378224	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0001250	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0001252	PMID:11738357	PCS		1/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-06]
OMIM:609285	Nemaline myopathy 4		HP:0003691	OMIM:609285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609285	Congenital myopathy 23		HP:0003593	PMID:23378224	PCS		2/7			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0001290	OMIM:609285	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609285	Congenital myopathy 23		HP:0033685	PMID:23378224	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0003690	PMID:11738357	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-06]
OMIM:609285	Nemaline myopathy 4		HP:0001270	PMID:23378224	PCS		1/1			P	HPO:skoehler[2010-06-20]
OMIM:609285	Nemaline myopathy 4		HP:0003391	OMIM:609285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609285	Congenital myopathy 23		HP:0034045	PMID:23378224	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0011463	PMID:23378224	PCS		2/7			C	HPO:skoehler[2015-12-30];HPO:probinson[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0007340	PMID:23378224	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0001349	OMIM:609285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609285	Nemaline myopathy 4		HP:0008872	PMID:11738357	PCS		1/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-06]
OMIM:609285	Nemaline myopathy 4		HP:0002515	OMIM:609285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609285	Nemaline myopathy 4		HP:0000218	OMIM:609285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609285	Nemaline myopathy 4		HP:0003803	PMID:23378224	PCS		1/7			P	HPO:skoehler[2010-06-19]
OMIM:609285	Congenital myopathy 23		HP:0003701	PMID:23378224	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0001763	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0001265	OMIM:609285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609285	Nemaline myopathy 4		HP:0002751	OMIM:609285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609285	Nemaline myopathy 4		HP:0002058	OMIM:609285	IEA		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-06]
OMIM:609285	Nemaline myopathy 4		HP:0003202	OMIM:609285	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609285	Congenital myopathy 23		HP:0003687	PMID:23378224	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0002015	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0003621	PMID:11738357	PCS		1/2			C	HPO:probinson[2022-08-06];HPO:probinson[2022-08-06]
OMIM:609285	Congenital myopathy 23		HP:0031318	PMID:23378224	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0002650	PMID:23378224	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0031936	PMID:23378224	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0001288	PMID:11738357	PCS	HP:0003621	1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-06]
OMIM:609285	Congenital myopathy 23		HP:0001288	PMID:23378224	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0001288	PMID:23378224	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0002792	OMIM:609285	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609285	Congenital myopathy 23		HP:0012378	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0000709	PMID:23378224	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0034392	PMID:23378224	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0100753	PMID:23378224	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0030230	PMID:23378224	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0003738	PMID:23378224	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0002527	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0000768	PMID:23378224	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0030051	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Congenital myopathy 23		HP:0002942	PMID:23378224	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:609285	Nemaline myopathy 4		HP:0000006	PMID:11738357	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-06]
OMIM:609285	Nemaline myopathy 4		HP:0003798	PMID:11738357;PMID:23378224	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:skoehler[2010-06-20];HPO:probinson[2022-08-06]
OMIM:609285	Nemaline myopathy 4		HP:0000467	PMID:11738357	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-06]
OMIM:125520	Cayler cardiofacial syndrome		HP:0003577	OMIM:125520	TAS					C	HPO:probinson[2012-04-11]
OMIM:125520	Cayler cardiofacial syndrome		HP:0001629	OMIM:125520	TAS					P	HPO:probinson[2012-04-11]
OMIM:125520	Cayler cardiofacial syndrome		HP:0001636	OMIM:125520	TAS					P	HPO:probinson[2012-04-11]
OMIM:125520	Cayler cardiofacial syndrome		HP:0011333	OMIM:125520	TAS					P	HPO:probinson[2012-04-11]
OMIM:125520	Cayler cardiofacial syndrome		HP:0001643	OMIM:125520	TAS					P	HPO:probinson[2012-04-11]
OMIM:125520	Cayler cardiofacial syndrome		HP:0000006	OMIM:125520	TAS					I	HPO:probinson[2012-04-11]
OMIM:209700	Atrophoderma vermiculata		HP:0001056	OMIM:209700	TAS					P	HPO:skoehler[2015-04-19]
OMIM:209700	Atrophoderma vermiculata		HP:0000271	OMIM:209700	IEA					P	HPO:iea[2009-02-17]
OMIM:209700	Atrophoderma vermiculata		HP:0000007	OMIM:209700	IEA					I	HPO:iea[2009-02-17]
OMIM:209700	Atrophoderma vermiculata		HP:0100837	OMIM:209700	IEA					P	HPO:skoehler[2015-01-21]
OMIM:209700	Atrophoderma vermiculata		HP:0001626	OMIM:209700	IEA					P	HPO:iea[2009-02-17]
OMIM:209700	Atrophoderma vermiculata		HP:0000006	OMIM:209700	TAS					I	HPO:skoehler[2015-12-30]
OMIM:209700	Atrophoderma vermiculata		HP:0000951	OMIM:209700	IEA					P	HPO:iea[2009-02-17]
OMIM:209700	Atrophoderma vermiculata		HP:0001820	OMIM:209700	TAS					P	HPO:skoehler[2015-04-19]
OMIM:603964	Deafness, autosomal dominant 16		HP:0000360	OMIM:603964	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:603964	Deafness, autosomal dominant 16		HP:0008615	OMIM:603964	IEA					P	HPO:skoehler[2013-01-09]
OMIM:603964	Deafness, autosomal dominant 16		HP:0000006	OMIM:603964	IEA					I	HPO:skoehler[2013-01-10]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000010	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000076	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000175	OMIM:244600	TAS					P	HPO:skoehler[2012-08-01]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0005852	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000563	OMIM:244600	IEA					P	HPO:skoehler[2015-01-27]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0001156	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0005640	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0001263	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000470	OMIM:244600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000316	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000007	OMIM:244600	IEA					I	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0004209	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0008511	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000465	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0001510	OMIM:244600	IEA					P	HPO:iea[2009-02-17]
OMIM:244600	Keratoconus posticus circumscriptus		HP:0000204	OMIM:244600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000286	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000486	PMID:20018682	PCS		5/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0004322	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000122	PMID:20018682	PCS		2/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001252	PMID:20018682	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0003196	PMID:20018682	PCS		11/11			P	HPO:probinson[2012-04-25];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002937	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000316	PMID:20018682	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001845	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2012-11-26]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000998	PMID:20018682	PCS		7/11		HP:0012825	P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0100807	PMID:20018682	PCS		6/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0008897	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000912	PMID:20018682	PCS		8/10			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001643	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001763	PMID:20018682	PCS		11/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001249	PMID:20018682	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000358	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002553	PMID:20018682	PCS		11/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001265	PMID:20018682	PCS		9/10			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000175	PMID:20018682	PCS		3/11			P	HPO:probinson[2012-04-25];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000252	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001187	PMID:20018682	PCS		6/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001344	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000574	PMID:20018682	PCS		11/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000892	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002079	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0011968	PMID:20018682	PCS		11/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001382	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000294	PMID:20018682	PCS		11/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002948	PMID:20018682	PCS		6/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000327	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000767	PMID:20018682	PCS		9/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000007	PMID:20018682	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000403	PMID:20018682	PCS		8/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000527	PMID:20018682	PCS		11/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0006347	PMID:20018682	PCS		11/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000960	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000248	PMID:20018682	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000204	PMID:20018682	PCS		3/11			P	HPO:probinson[2012-04-25];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000369	PMID:20018682	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0004568	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000049	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000445	OMIM:213980	TAS					P	HPO:probinson[2012-04-25]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000341	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000582	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0003577	PMID:20018682	PCS		11/11			C	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000023	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000463	PMID:20018682	PCS		11/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002162	PMID:20018682	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001270	PMID:20018682	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0012368	PMID:20018682	PCS		11/11			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002080	PMID:20018682	PCS		6/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000739	PMID:20018682	PCS		7/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0012450	PMID:20018682	PCS		7/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000218	PMID:20018682	PCS		11/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000774	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0006610	OMIM:213980	TAS					P	HPO:skoehler[2014-06-24]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000212	PMID:20018682	PCS		8/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000256	PMID:20018682	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002558	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001363	PMID:20018682	PCS		2/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001561	PMID:20018682	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001520	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002650	PMID:20018682	PCS		7/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001762	PMID:20018682	PCS		3/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000431	PMID:20018682	PCS		11/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001288	PMID:20018682	PCS		11/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001162	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000470	PMID:20018682	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0002290	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0011504	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0011108	PMID:20018682	PCS		9/11			P	HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000902	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000508	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001558	PMID:20018682	PCS	HP:0011461	4/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000824	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001319	OMIM:213980	TAS					P	HPO:skoehler[2014-06-24]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000664	PMID:20018682	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0001631	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0007018	PMID:20018682	PCS		1/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-07]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000347	OMIM:213980	IEA					P	HPO:iea[2009-02-17]
OMIM:213980	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1		HP:0000742	OMIM:213980	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:617911	Diamond-Blackfan anemia-like		HP:0033074	PMID:28283061	PCS	HP:0003593	1/1			P	HPO:probinson[2020-09-20];HPO:probinson[2020-09-20]
OMIM:617911	Diamond-Blackfan anemia-like		HP:0012410	PMID:28283061	PCS		1/1			P	HPO:probinson[2020-09-20]
OMIM:617911	Diamond-Blackfan anemia-like		HP:0003593	PMID:28283061	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-20]
OMIM:617911	Diamond-Blackfan anemia-like		HP:0000007	PMID:28283061	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-20]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0001276	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0002510	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0002521	OMIM:601815	PCS					P	HPO:probinson[2012-04-11]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0001250	OMIM:601815	PCS					P	HPO:probinson[2012-04-11]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0001181	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0034691	OMIM:601815	TAS					P	HPO:probinson[2023-03-31]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0000639	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0011451	OMIM:601815	PCS					P	HPO:probinson[2012-04-11]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0000519	OMIM:601815	PCS					P	HPO:probinson[2012-04-11]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0001889	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0007266	OMIM:601815	PCS					P	HPO:probinson[2012-04-11]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0000007	OMIM:601815	IEA					I	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0008734	OMIM:601815	PCS					P	HPO:probinson[2012-04-11]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0001510	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0001873	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:601815	Phosphoglycerate dehydrogenase deficiency		HP:0001249	OMIM:601815	IEA					P	HPO:iea[2009-02-17]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002188	PMID:36745868;PMID:36517554	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002783	PMID:36745868;PMID:36517554	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0003212	PMID:36745868	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001272	PMID:36745868;PMID:36517554	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001250	PMID:36745868;PMID:36517554	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002240	PMID:36745868;PMID:36517554	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0003593	PMID:36745868;PMID:36517554	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0031250	PMID:36745868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001889	PMID:36745868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001888	PMID:36745868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0008897	PMID:36745868	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002514	PMID:36745868	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0200042	PMID:36745868;PMID:36517554	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001744	PMID:36745868;PMID:36517554	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0004315	PMID:36745868;PMID:36517554	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0003623	PMID:36517554	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001980	PMID:36517554	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002059	PMID:36745868;PMID:36517554	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0000670	PMID:36745868;PMID:36517554	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002155	PMID:36517554	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001047	PMID:36745868	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001263	PMID:36745868;PMID:36517554	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0011900	PMID:36517554	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0003281	PMID:36517554	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0040087	PMID:36517554	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0032154	PMID:36745868;PMID:36517554	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0500093	PMID:36745868	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001954	PMID:36745868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0000007	PMID:36517554	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0001873	PMID:36745868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002721	PMID:36745868;PMID:36517554	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620603	Immunodeficiency 114, folate-responsive		HP:0002028	PMID:36745868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619082	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1		HP:0003577	PMID:30945270	PCS		4/4			C	HPO:probinson[2021-01-01]
OMIM:619082	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1		HP:0000518	PMID:30945270	PCS		4/4			P	HPO:probinson[2021-01-01]
OMIM:619082	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1		HP:0000482	PMID:30945270	PCS	HP:0003577	4/4			P	HPO:probinson[2021-01-01]
OMIM:619082	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1		HP:0007663	PMID:30945270	PCS	HP:0003621	4/4			P	HPO:probinson[2021-01-01]
OMIM:619082	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1		HP:0000510	PMID:30945270	PCS		4/4			P	HPO:probinson[2021-01-01]
OMIM:619082	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1		HP:0000006	PMID:30945270	PCS					I	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619082	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1		HP:0030856	PMID:30945270	PCS		1/4			P	HPO:probinson[2021-01-01]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001133	PMID:25926518	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000121	PMID:11836330	PCS		3/11			P	HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000121	PMID:19758376	PCS	HP:0003621	5/13			P	HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000121	PMID:18616706	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008209	PMID:16965330;PMID:2348835;PMID:18616706;PMID:19807739	PCS		17/24			P	HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002024	PMID:16965330;PMID:28540407;PMID:2348835;PMID:18616706;PMID:11836330;PMID:19807739	PCS		22/106			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002582	PMID:22024611;PMID:18616706;PMID:11836330	PCS		8/29			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001096	PMID:16965330;PMID:19758376;PMID:11836330	PCS		8/29			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001250	PMID:18616706	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0003472	PMID:28540407	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0003593	PMID:19758376	PCS		1/13			C	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001094	PMID:19758376	PCS	HP:0011463	1/13			P	HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0100651	PMID:19758376	PCS	HP:0011463	3/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0100651	PMID:2348835	PCS		8/68			P	HPO:probinson[2020-11-11]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0100651	PMID:19807739	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0100651	PMID:18616706	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0006270	PMID:19807739	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000518	PMID:16965330;PMID:28540407;PMID:11836330	PCS		8/28			P	ORCID:0000-0002-0736-9199[2024-05-10];HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0011463	PMID:9543115;PMID:16965330;PMID:28540407;PMID:19758376;PMID:18616706;PMID:22024611;PMID:19807739	PCS		39/67			C	HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0034189	PMID:22024611	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0100647	PMID:22024611;PMID:18616706	PCS		3/19			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0100806	PMID:19807739	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0020123	PMID:2348835	PCS		22/68			P	HPO:probinson[2020-11-11]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001803	PMID:19807739	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0004319	PMID:28740581	PCS					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-25]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:5000011	PMID:19758376;PMID:19807739	PCS		3/21			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0003623	PMID:19758376;PMID:18616706	PCS		9/27			C	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000134	PMID:11836330	PCS			FEMALE		P	HPO:iea[2009-02-17];HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002232	PMID:22024611	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0025379	PMID:19758376;PMID:22024611;PMID:19807739	PCS		7/25			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0100582	PMID:19807739	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0030629	PMID:25926518	PCS					P	HPO:probinson[2020-09-28];HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0009098	PMID:2348835	PCS		68/68			P	HPO:probinson[2020-11-11]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000007	PMID:11836330	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000403	PMID:19807739	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000846	PMID:2348835	PCS		49/68			P	HPO:probinson[2020-11-11]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008404	PMID:2348835;PMID:22024611	PCS		35/72			P	HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000006	PMID:19758376	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001733	PMID:16965330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0034071	PMID:22024611;PMID:19807739	PCS		5/12			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008207	PMID:11836330	PCS		9/11			P	HPO:skoehler[2010-06-20];HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008207	PMID:19758376	PCS	HP:0003621	5/13			P	HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008207	PMID:16965330	PCS		7/15			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008207	PMID:28540407	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008207	PMID:22024611	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008207	PMID:19807739	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0008207	PMID:18616706	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002289	PMID:19758376	PCS	HP:0003621	7/13			P	HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002289	PMID:22024611	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001596	PMID:16965330;PMID:2348835;PMID:18616706;PMID:11836330;PMID:19807739	PCS		38/106			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000580	PMID:25926518	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:4000030	PMID:19758376	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0012203	PMID:19758376;PMID:22024611	PCS		3/17			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0006297	PMID:28540407;PMID:2348835;PMID:22024611;PMID:11836330;PMID:19807739	PCS		67/93			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001746	PMID:9543115;PMID:18616706	PCS		10/25			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0007663	PMID:25926518	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0200120	PMID:9543115;PMID:16965330	PCS		14/47			P	HPO:skoehler[2013-06-11];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000135	PMID:22024611	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002014	PMID:28540407;PMID:1941421;PMID:22024611;PMID:19807739	PCS		14/24			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001045	PMID:2348835;PMID:22024611;PMID:18616706;PMID:11836330;PMID:19807739	PCS		17/107			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0003621	PMID:16965330;PMID:22024611;PMID:18616706;PMID:19807739	PCS		18/43			C	ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0031817	PMID:28740581;PMID:19758376	PCS		23/23			P	HPO:lccarmody[2018-09-25];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:6000343	PMID:19758376;PMID:18616706;PMID:22024611;PMID:19807739	PCS		8/29			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0001081	PMID:9543115;PMID:18616706;PMID:19807739	PCS		11/34			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0032069	PMID:19758376;PMID:22024611	PCS		3/17			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0011109	PMID:19807739	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0033637	PMID:19758376	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000829	PMID:16965330;PMID:28540407;PMID:19758376;PMID:2348835;PMID:18616706;PMID:22024611;PMID:11836330;PMID:19807739	PCS		121/136			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24];HPO:probinson[2020-11-11];HPO:probinson[2020-09-28];ORCID:0000-0002-0736-9199[2024-05-10];ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0034055	PMID:19807739	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002728	PMID:11836330	PCS		11/11			P	HPO:iea[2009-02-17];HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002728	PMID:19758376	PCS	HP:0003623	10/13			P	HPO:probinson[2020-09-28]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002728	PMID:18616706	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002728	PMID:22024611	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002728	PMID:19807739	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002608	PMID:19758376	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002925	PMID:19758376	PCS		3/13			P	ORCID:0000-0002-0736-9199[2024-11-20]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000821	PMID:19758376;PMID:2348835;PMID:11836330;PMID:19807739	PCS		13/101			P	HPO:probinson[2020-11-11];HPO:probinson[2020-09-28];ORCID:0000-0002-0736-9199[2024-11-20];HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0000026	PMID:11836330	PCS			MALE		P	HP:probinson[2019-02-24]
OMIM:240300	Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia		HP:0002841	PMID:16965330	PCS		14/15			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615860	Cone-Rod dystrophy 19		HP:0003596	PMID:24791901	PCS		1/5			C	HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0011463	PMID:24791901	PCS		2/5			C	HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0011462	PMID:24791901	PCS		2/5			C	HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0000007	PMID:24791901	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0007663	PMID:24791901	PCS		5/5			P	HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0030629	PMID:24791901	PCS					P	HPO:probinson[2022-10-07];HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0000548	PMID:24791901	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0011003	PMID:24791901	PCS		2/5			P	HPO:probinson[2022-10-07]
OMIM:615860	Cone-Rod dystrophy 19		HP:0030844	PMID:24791901	PCS		4/4			P	HPO:probinson[2022-10-07]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0001265	OMIM:617087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0003477	OMIM:617087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0000365	PMID:18458227	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0002650	PMID:18458227	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0003387	PMID:18458227	PCS		2/2			P	HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0001762	PMID:18458227	PCS		2/3			P	HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0001288	PMID:18458227	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0001761	OMIM:617087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0002194	OMIM:617087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0002808	PMID:18458227	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0011463	PMID:18458227	PCS		3/3			C	HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0007210	PMID:18458227	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0009027	OMIM:617087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0000007	PMID:18458227	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0002936	PMID:18458227	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0000648	OMIM:617087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0002747	OMIM:617087	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0000543	OMIM:617087	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0003701	PMID:18458227	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0001620	PMID:18458227	PCS		2/3			P	HPO:probinson[2023-04-18]
OMIM:617087	Charcot-Marie-Tooth disease, axonal, type 2A2B		HP:0009129	PMID:18458227	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:616399	Brugada syndrome 9		HP:0003596	PMID:21349352	PCS		1/2			C	HPO:probinson[2022-09-08]
OMIM:616399	Brugada syndrome 9		HP:0012251	PMID:21349352	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:616399	Brugada syndrome 9		HP:0011462	PMID:21349352	PCS		1/2			C	HPO:probinson[2022-09-08]
OMIM:616399	Brugada syndrome 9		HP:0001657	PMID:21349352	PCS		1/2			P	HPO:probinson[2022-09-08]
OMIM:616399	Brugada syndrome 9		HP:0031972	PMID:21349352	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:616399	Brugada syndrome 9		HP:0001962	PMID:21349352	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-08]
OMIM:616399	Brugada syndrome 9		HP:0000006	PMID:21349352	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:615848	Melanoma, cutaneous malignant, susceptibility to, 10		HP:0002861	PMID:24686849	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-27]
OMIM:615848	Melanoma, cutaneous malignant, susceptibility to, 10		HP:0003581	PMID:24686849	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:615848	Melanoma, cutaneous malignant, susceptibility to, 10		HP:0003829	PMID:24686849	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:615848	Melanoma, cutaneous malignant, susceptibility to, 10		HP:0100245	PMID:37140166	PCS					P	HPO:probinson[2024-08-03]
OMIM:615848	Melanoma, cutaneous malignant, susceptibility to, 10		HP:0000006	PMID:24686849	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:613587	Occult macular dystrophy		HP:0007924	PMID:20826268	PCS					P	HPO:skoehler[2013-05-31]
OMIM:613587	Occult macular dystrophy		HP:0030468	PMID:20826268	PCS					P	HPO:probinson[2017-12-11]
OMIM:613587	Occult macular dystrophy		HP:0003621	PMID:20826268	PCS		5/16			C	HPO:probinson[2024-03-14]
OMIM:613587	Occult macular dystrophy		HP:0003596	PMID:20826268	PCS		3/16			C	HPO:probinson[2024-03-14]
OMIM:613587	Occult macular dystrophy		HP:0030466	PMID:20826268	PCS		0/16			P	HPO:skoehler[2015-07-26];HPO:probinson[2024-03-14]
OMIM:613587	Occult macular dystrophy		HP:0011462	PMID:20826268	PCS		8/16			C	HPO:probinson[2024-03-14]
OMIM:613587	Occult macular dystrophy		HP:0007754	PMID:20826268	PCS		HP:0040281			P	HPO:probinson[2017-12-11]
OMIM:613587	Occult macular dystrophy		HP:0030604	PMID:20826268	PCS		0/16			P	HPO:probinson[2017-12-11];HPO:probinson[2024-03-14]
OMIM:613587	Occult macular dystrophy		HP:0000006	PMID:20826268	PCS					I	HPO:probinson[2017-12-11]
OMIM:613587	Occult macular dystrophy		HP:0003831	PMID:20826268	PCS					I	HPO:probinson[2024-08-13]
OMIM:612841	Hypotrichosis 5		HP:0000164	PMID:23099647	PCS		0/9			P	HPO:skoehler[2019-04-18]
OMIM:612841	Hypotrichosis 5		HP:0003577	PMID:23099647	PCS		1/1			C	HPO:probinson[2023-02-18]
OMIM:612841	Hypotrichosis 5		HP:0002221	PMID:23099647	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:612841	Hypotrichosis 5		HP:0001597	PMID:23099647	PCS		0/9			P	HPO:skoehler[2019-04-18]
OMIM:612841	Hypotrichosis 5		HP:0000364	PMID:23099647	PCS		0/9			P	HPO:skoehler[2019-04-18]
OMIM:612841	Hypotrichosis 5		HP:0001596	PMID:23099647	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:612841	Hypotrichosis 5		HP:0000653	PMID:23099647	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:612841	Hypotrichosis 5		HP:0000971	PMID:23099647	PCS		0/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:612841	Hypotrichosis 5		HP:0045074	PMID:23099647	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:612841	Hypotrichosis 5		HP:0000006	PMID:23099647	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:612841	Hypotrichosis 5		HP:0002555	PMID:23099647	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0000011	PMID:22448145	PCS		13/23			P	HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0003621	PMID:22448145	PCS		10/54			C	HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0002650	PMID:22448145	PCS		9/54			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0003596	PMID:22448145	PCS		14/54			C	HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0000365	PMID:22448145	PCS		3/23		HP:0012825	P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0000012	PMID:22448145	PCS		26/54			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0002497	PMID:22448145	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0001332	PMID:22448145	PCS		15/54			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0001310	PMID:22448145	PCS		31/54			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0002120	PMID:22448145	PCS		10/23			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0001272	PMID:22448145	PCS		40/54			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0002352	PMID:22448145	PCS		21/54			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0002066	PMID:22448145	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0001260	PMID:22448145	PCS		42/54			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0001251	PMID:22448145	PCS		54/54			P	HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0100543	PMID:22448145	PCS		10/23			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0011463	PMID:22448145	PCS		11/54			C	HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0011462	PMID:22448145	PCS		19/54			C	HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0000007	PMID:22448145	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0002505	PMID:22448145	PCS		21/54			P	HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0001257	PMID:22448145	PCS		54/54			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0000666	PMID:22448145	PCS		24/54		HP:0012825	P	HPO:skoehler[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0001347	PMID:22448145	PCS		23/23			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-30]
OMIM:611390	Spastic ataxia 3, autosomal recessive		HP:0006855	PMID:22448145	PCS		50/54			P	HPO:probinson[2022-10-30]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0001265	OMIM:300718	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003236	OMIM:300718	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003621	PMID:18952429	PCS		1/1			C	HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0002650	PMID:18952429	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0001371	PMID:18952429	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0000470	OMIM:300718	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0034320	PMID:18274675	PCS		2/2			P	HPO:probinson[2022-09-05]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0002808	OMIM:300718	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0009046	PMID:18952429	PCS		1/1			P	HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003805	PMID:18952429	PCS		1/1			P	HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003307	OMIM:300718	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0002747	PMID:18952429	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0001417	PMID:18274675	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0002359	OMIM:300718	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003701	PMID:18952429	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003306	PMID:18952429	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0001644	PMID:18274675	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-15]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003557	OMIM:300718	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300718	Myopathy, reducing body, X-linked, childhood-onset		HP:0003678	OMIM:300718	IEA					C	HPO:skoehler[2010-06-19]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001276	PMID:11889467	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002421	PMID:11889467	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0003577	PMID:11889467	PCS		1/1			C	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002521	PMID:17668384	PCS	HP:0003593	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002521	PMID:21108397	PCS		2/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002521	PMID:11889467	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002188	PMID:11889467	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001332	OMIM:308350	IEA					P	HPO:iea[2009-02-17]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002123	OMIM:308350	IEA					P	HPO:skoehler[2010-06-18]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002283	PMID:21108397	PCS		2/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0012469	PMID:11889467	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0000817	PMID:11889467	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002119	OMIM:308350	IEA					P	HPO:iea[2009-02-17]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001249	PMID:21108397	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001347	OMIM:308350	IEA					P	HPO:iea[2009-02-17]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0003623	PMID:21108397;PMID:17668384	PCS		4/4			C	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0008936	OMIM:308350	IEA					P	HPO:iea[2009-02-17]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002015	OMIM:308350	IEA					P	HPO:iea[2009-02-17]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0000252	PMID:21108397;PMID:11889467;OMIM:308350	PCS		13/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-22];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0000054	PMID:21108397;PMID:17668384	PCS		2/4			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001266	OMIM:308350	IEA					P	HPO:iea[2009-02-17]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0025357	PMID:21108397	PCS		1/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001263	PMID:21108397;PMID:11889467	PCS		3/3			P	HPO:probinson[2022-06-22];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001285	PMID:21108397	PCS		1/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0002094	OMIM:308350	IEA					P	HPO:iea[2009-02-17]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0010851	PMID:21108397;PMID:17668384	PCS		4/4			P	HPO:probinson[2021-06-23];HPO:probinson[2021-06-23];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0011344	PMID:17668384	PCS		2/2			P	HPO:probinson[2021-06-23];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0100660	OMIM:308350	TAS					P	HPO:skoehler[2018-10-08]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001419	PMID:11889467	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0032792	PMID:17668384	PCS	HP:0003623	2/2			P	HPO:probinson[2021-06-23];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0011153	PMID:21108397	PCS		1/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0007256	PMID:21108397	PCS		1/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0000568	PMID:11889467	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0200134	PMID:17668384	PCS		2/2			P	HPO:skoehler[2015-01-19];HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0200134	PMID:21108397	PCS	HP:0003623	2/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001357	PMID:11889467	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0007359	PMID:21108397	PCS		2/2			P	HPO:probinson[2021-06-23]
OMIM:308350	Developmental and epileptic encephalopathy 1		HP:0001510	PMID:21108397	PCS		1/2			P	HPO:probinson[2021-06-23]
OMIM:105800	Aneurysm, intracranial berry, 1		HP:0002170	OMIM:105800	IEA					P	HPO:iea[2009-02-17]
OMIM:105800	Aneurysm, intracranial berry, 1		HP:0004944	OMIM:105800	IEA					P	HPO:iea[2009-02-17]
OMIM:105800	Aneurysm, intracranial berry, 1		HP:0000006	OMIM:105800	IEA					I	HPO:iea[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0000121	OMIM:239199	IEA					P	HPO:iea[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0002013	OMIM:239199	IEA					P	HPO:iea[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0001508	OMIM:239199	IEA					P	HPO:iea[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0001947	OMIM:239199	IEA					P	HPO:iea[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0000007	OMIM:239199	IEA					I	HPO:iea[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0000843	OMIM:239199	TAS					P	HPO:probinson[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0002150	OMIM:239199	IEA					P	HPO:iea[2009-02-17]
OMIM:239199	Hyperparathyroidism, neonatal self-limited primary, with hypercalciuria		HP:0003072	OMIM:239199	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001331	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0000286	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0002069	PMID:22177091	PCS		1/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001176	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001377	PMID:22177091	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001212	PMID:22177091	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000486	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0002188	PMID:22177091	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001250	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001252	PMID:22177091	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001290	OMIM:277590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277590	Weaver syndrome		HP:0001848	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0011461	PMID:22177091	PCS		3/3			C	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000316	PMID:22177091	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001845	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0000954	PMID:22177091	PCS		0/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0009466	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001643	PMID:22177091	PCS		1/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001840	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0000278	PMID:22177091	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000311	OMIM:277590	TAS					P	HPO:probinson[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001249	OMIM:277590	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277590	Weaver syndrome		HP:0000995	PMID:22177091	PCS		2/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001540	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0005469	PMID:22177091	PCS		2/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000494	PMID:22177091	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0002673	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001260	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001263	OMIM:277590	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277590	Weaver syndrome		HP:0002591	PMID:22177091	PCS		2/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0010751	OMIM:277590	TAS					P	HPO:probinson[2012-04-30]
OMIM:277590	Weaver syndrome		HP:0012385	PMID:22177091	PCS		3/3			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001816	PMID:22177091	PCS		3/3			P	HPO:probinson[2013-08-09];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001537	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0006387	PMID:22177091	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001814	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001615	PMID:22177091	PCS		3/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0005616	PMID:22177091	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000400	PMID:22177091	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0003911	OMIM:277590	TAS					P	HPO:probinson[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0002866	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001257	OMIM:277590	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277590	Weaver syndrome		HP:0000006	PMID:22177091	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0004689	PMID:22177091	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001276	PMID:22177091	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000343	PMID:22177091	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000023	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0002121	PMID:22177091	PCS		1/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0001350	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0010300	OMIM:277590	TAS					P	HPO:probinson[2014-05-24]
OMIM:277590	Weaver syndrome		HP:0008070	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001548	PMID:22177091	PCS	HP:0011461	3/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0002834	OMIM:277590	TAS					P	HPO:probinson[2015-03-21]
OMIM:277590	Weaver syndrome		HP:0002119	PMID:22177091	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0030084	OMIM:277590	TAS					P	HPO:skoehler[2014-09-21]
OMIM:277590	Weaver syndrome		HP:0200000	OMIM:277590	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277590	Weaver syndrome		HP:0001863	PMID:22177091	PCS		2/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000256	PMID:22177091	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000773	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0000973	PMID:22177091	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0006956	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0002213	PMID:22177091;OMIM:277590	PCS		11/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000750	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0002650	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001762	PMID:22177091	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000034	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001761	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0001321	PMID:22177091	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0003066	PMID:22177091	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0003186	PMID:22177091	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0002172	PMID:22177091	PCS		3/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0005280	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0011304	PMID:22177091	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000708	OMIM:277590	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277590	Weaver syndrome		HP:0009473	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0002808	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0007010	PMID:22177091	PCS		3/3			P	HPO:probinson[2022-08-28]
OMIM:277590	Weaver syndrome		HP:0000028	OMIM:277590	IEA					P	HPO:iea[2009-02-17]
OMIM:277590	Weaver syndrome		HP:0000303	OMIM:277590	TAS					P	HPO:probinson[2012-04-30]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001397	PMID:27426735	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001410	PMID:27426735	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0030674	PMID:27426735	PCS		3/3			C	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001250	PMID:27426735	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0003155	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001395	PMID:27426735	PCS		2/3			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001252	PMID:27426735	PCS		2/3			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0003073	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0011433	PMID:27891590	PCS		1/1			H	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0000081	PMID:27891590	PCS		1/1			P	HPO:skoehler[2019-02-22]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0031964	PMID:27891590;PMID:27426735	PCS		2/4			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001508	PMID:27426735	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001987	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001943	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0008897	PMID:27426735	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001406	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0000311	PMID:27891590	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001249	PMID:27426735	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0000952	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001562	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0031956	PMID:27891590;PMID:27426735	PCS		2/4			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001344	PMID:27426735	PCS		1/3			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0000293	PMID:27891590;PMID:27426735	PCS		2/4			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001382	PMID:27891590	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001263	PMID:27426735	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0005484	PMID:27426735	PCS		3/3			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0030948	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0031831	PMID:27426735	PCS		3/3			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0002908	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0034198	PMID:27891590	PCS		1/1			C	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0000407	PMID:27426735	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001518	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0011451	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0000007	PMID:27426735	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001511	PMID:27426735	PCS	HP:0030674	3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001511	PMID:27891590	PCS		1/1			P	HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0001257	PMID:27426735	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-07]
OMIM:617093	Growth retardation, impaired intellectual development, hypotonia, and hepatopathy		HP:0000126	PMID:27891590	PCS		1/1			P	HPO:skoehler[2019-02-22]
OMIM:616602	Craniosynostosis 6		HP:0003577	PMID:26340333	PCS		3/9			C	HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000486	PMID:26340333	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0001272	PMID:26340333	PCS				HP:0012825	P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0003298	PMID:26340333	PCS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0001274	PMID:26340333	PCS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0001252	PMID:26340333	PCS		3/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000262	OMIM:616602	TAS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0003593	PMID:26340333	PCS		6/9			C	HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0011318	PMID:26340333	PCS		6/9			P	HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000316	PMID:26340333	PCS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0001305	PMID:26340333	PCS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0001363	PMID:26340333	PCS		9/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000252	PMID:26340333	PCS		3/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0002697	PMID:26340333	PCS		1/9			P	HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0006956	PMID:26340333	PCS		2/9			P	HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0002650	PMID:26340333	PCS		2/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000270	PMID:26340333	PCS		2/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0001263	PMID:26340333	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000294	PMID:26340333	PCS		2/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0011322	PMID:26340333	PCS		1/9			P	HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000407	PMID:26340333	PCS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000508	PMID:26340333	PCS		3/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000348	PMID:26340333	PCS		3/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0001357	PMID:26340333	PCS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000006	PMID:26340333	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:616602	Craniosynostosis 6		HP:0000248	PMID:26340333	PCS		1/9			P	HPO:skoehler[2015-11-29];HPO:probinson[2023-02-10]
OMIM:619531	Cone-rod dystrophy 22		HP:0003621	PMID:33077892	PCS		1/4			C	HPO:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0030631	PMID:33077892	PCS		1/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0025159	PMID:33077892	PCS		2/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0030629	PMID:33077892	PCS		1/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0030825	PMID:33077892	PCS		1/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0011504	PMID:33077892	PCS		1/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0030844	PMID:33077892	PCS		1/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0011462	PMID:33077892	PCS		3/4			C	HPO:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0000613	PMID:33077892	PCS		2/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0000007	PMID:33077892	PCS					I	HPO:probinson[2021-10-24];HPO:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0007663	PMID:33077892	PCS		4/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0007722	PMID:33077892	PCS		1/4			P	HP:probinson[2021-10-24]
OMIM:619531	Cone-rod dystrophy 22		HP:0007843	PMID:33077892	PCS		1/4			P	HP:probinson[2021-10-24]
OMIM:600060	Deafness, neurosensory, autosomal recessive 2		HP:0003577	OMIM:600060	TAS					C	HPO:skoehler[2009-02-17]
OMIM:600060	Deafness, neurosensory, autosomal recessive 2		HP:0001751	OMIM:600060	TAS					P	HPO:skoehler[2013-12-09]
OMIM:600060	Deafness, neurosensory, autosomal recessive 2		HP:0002321	OMIM:600060	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600060	Deafness, neurosensory, autosomal recessive 2		HP:0000407	OMIM:600060	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600060	Deafness, neurosensory, autosomal recessive 2		HP:0000007	OMIM:600060	TAS					I	HPO:skoehler[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002982	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003015	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0006603	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0004566	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0001377	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0008905	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002980	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002651	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002750	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002970	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003031	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003021	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003071	OMIM:602111	TAS					P	HPO:probinson[2013-04-08]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0010585	OMIM:602111	TAS					P	HPO:probinson[2013-04-08]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0000926	OMIM:602111	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002869	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0008476	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002515	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002812	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002758	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002986	OMIM:602111	TAS					P	HPO:probinson[2009-02-17]
OMIM:602111	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0000006	OMIM:602111	TAS					I	HPO:probinson[2009-02-17]
OMIM:600706	Proximal myopathy with focal depletion of mitochondria		HP:0003236	OMIM:600706	TAS					P	HPO:probinson[2009-02-17]
OMIM:600706	Proximal myopathy with focal depletion of mitochondria		HP:0003738	OMIM:600706	TAS				HP:0012828	P	HPO:probinson[2012-07-16]
OMIM:600706	Proximal myopathy with focal depletion of mitochondria		HP:0003701	OMIM:600706	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:600706	Proximal myopathy with focal depletion of mitochondria		HP:0000006	OMIM:600706	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001276	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001254	PMID:10071185	PCS		1/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0003654	PMID:10071185	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0003577	PMID:10071185	PCS		3/18			C	HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001250	PMID:10071185	PCS		10/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001274	OMIM:274270	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001252	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0003593	PMID:10071185	PCS		4/18			C	HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001270	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0012127	PMID:10071185	PCS					P	HPO:probinson[2020-10-13];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:6000119	PMID:9816152	PCS					P	HPO:probinson[2024-01-13]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001508	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000639	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0011463	PMID:10071185	PCS		6/18			C	HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000717	PMID:10071185	PCS		4/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000752	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001249	PMID:10071185	PCS		10/22			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0002059	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000252	PMID:10071185	PCS		3/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0003621	PMID:10071185	PCS		5/18			C	HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000750	PMID:10071185	PCS		3/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000007	OMIM:274270	IEA					I	HPO:iea[2009-02-17]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000568	PMID:10071185	PCS		1/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000648	PMID:10071185	PCS		1/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0001510	PMID:10071185	PCS		4/22			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0000589	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:274270	Dihydropyrimidine dehydrogenase deficiency		HP:0002445	OMIM:274270	IEA					P	HPO:skoehler[2010-06-18]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0003596	PMID:25227500	PCS		3/6			C	HPO:probinson[2023-03-08];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0007663	PMID:25227500	PCS		6/6			P	HPO:skoehler[2015-07-26]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0000007	PMID:25227500	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0000505	PMID:25227500	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0030629	PMID:25227500	PCS		1/6			P	HPO:probinson[2023-03-08];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0000603	PMID:25227500	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0025710	PMID:25227500	PCS		3/6			C	HPO:probinson[2023-03-08];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0011003	PMID:25227500	PCS		3/6			P	HPO:probinson[2023-03-08];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0000543	PMID:25227500	PCS		1/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0007754	PMID:25227500	PCS		6/6			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0000642	PMID:25227500	PCS		4/5			P	HPO:probinson[2023-03-08]
OMIM:616170	Macular dystrophy with central cone involvement		HP:0011504	PMID:25227500	PCS		2/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-08]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000365	PMID:32152250	PCS		3/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0002023	PMID:32152250	PCS		1/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000023	PMID:32152250	PCS		2/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0001250	PMID:32152250	PCS		1/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0001252	PMID:32152250	PCS		10/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0010862	PMID:32152250	PCS		14/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000219	PMID:32152250	PCS		5/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000256	PMID:32152250	PCS		2/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0002558	PMID:32152250	PCS		2/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0001249	PMID:32152250	PCS		17/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000252	PMID:32152250	PCS		3/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000494	PMID:32152250	PCS		4/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000750	PMID:32152250	PCS		16/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0001382	PMID:32152250	PCS		8/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0001263	PMID:32152250	PCS		17/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0002194	PMID:32152250	PCS		12/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000826	PMID:32152250	PCS		1/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000729	PMID:32152250	PCS		8/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000403	PMID:32152250	PCS		3/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0007018	PMID:32152250	PCS		11/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000006	PMID:32152250	PCS					I	HPO:probinson[2021-05-11];HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000347	PMID:32152250	PCS		5/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000325	PMID:32152250	PCS		3/17			P	HPO:probinson[2021-05-11]
OMIM:619243	Global developmental delay with speech and behavioral abnormalities		HP:0000028	PMID:32152250	PCS		1/12			P	HPO:probinson[2021-05-11]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0003477	OMIM:115150	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000365	PMID:19206169	PCS		3/15			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000486	PMID:19206169;PMID:18456719	PCS		9/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0004322	PMID:19206169;PMID:18456719;PMID:24800029	PCS		12/20			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001054	PMID:19206169	PCS		4/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0003196	PMID:18456719	PCS		2/2			P	HPO:probinson[2013-04-09];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002020	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0003593	PMID:18456719	PCS		2/2			C	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001290	PMID:19206169	PCS		13/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0006191	PMID:19206169	PCS		6/16			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000639	PMID:19206169	PCS		5/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000914	PMID:19206169	PCS		14/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0012471	PMID:19206169	PCS		8/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000635	PMID:18456719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000238	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001048	PMID:18456719	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002019	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0009748	PMID:19206169	PCS		12/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000358	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000494	PMID:19206169;PMID:18456719;PMID:24800029	PCS		11/20			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0007429	PMID:24800029	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001187	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000529	OMIM:115150	TAS					P	HPO:skoehler[2013-04-18]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000407	PMID:18456719	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000767	PMID:18456719;PMID:24800029	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21];ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0004209	PMID:24800029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000768	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000520	PMID:18456719	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000006	PMID:19206169	PCS					I	HPO:iea[2009-10-09];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000369	PMID:19206169;PMID:18456719;PMID:24800029	PCS		19/20			P	HPO:skoehler[2013-07-30];HPO:probinson[2020-08-10];ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000126	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001276	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000341	PMID:19206169;PMID:18456719	PCS		15/19			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0003577	PMID:16439621;PMID:16474404	PCS		27/27			C	HPO:probinson[2022-05-14];HPO:iea[2009-10-09];HP:probinson[2019-01-03]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000343	PMID:18456719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000463	OMIM:115150	TAS					P	HPO:probinson[2013-04-09]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002002	PMID:18456719;PMID:24800029	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21];ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002120	PMID:24800029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001270	PMID:18456719	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0008070	PMID:19206169;PMID:18456719	PCS		12/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:skoehler[2013-04-09];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0100703	OMIM:115150	TAS					P	HPO:skoehler[2013-07-30]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0100704	PMID:19206169	PCS		2/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0008872	PMID:19206169	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000975	PMID:19206169	PCS		9/11			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0008113	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000218	PMID:18456719;PMID:24800029	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21];ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000179	PMID:24800029	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001561	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001047	OMIM:115150	TAS				HP:0012828	P	HPO:probinson[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000475	PMID:18456719	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002650	PMID:19206169;PMID:18456719	PCS		4/18			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002013	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000194	OMIM:115150	TAS					P	HPO:skoehler[2013-07-30]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000470	PMID:19206169	PCS		11/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0011344	PMID:24800029	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0011471	PMID:19416762	PCS		10/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0007370	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0008064	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0032152	PMID:19206169	PCS		7/13			P	HPO:skoehler[2019-02-22];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000508	PMID:19206169;PMID:18456719;PMID:24800029	PCS		13/20			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000465	PMID:19206169;PMID:18456719	PCS		13/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000347	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002223	PMID:19206169;PMID:18456719	PCS		16/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000561	OMIM:115150	IEA					P	HPO:iea[2012-03-02]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000286	PMID:19206169;PMID:18456719;PMID:24800029	PCS		13/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000164	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001250	PMID:19206169	PCS		9/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001252	PMID:19206169;PMID:18456719	PCS		14/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0010807	OMIM:115150	TAS					P	HPO:skoehler[2013-07-30]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0030939	PMID:19206169	PCS		13/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0004482	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000280	PMID:24800029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001093	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0045075	PMID:24800029	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0007481	PMID:18456719	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000958	PMID:18456719	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000957	PMID:18456719	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0011220	PMID:19206169	PCS		10/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000717	PMID:18456719	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000316	PMID:19206169;PMID:18456719	PCS		14/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000953	PMID:19206169	PCS		6/17			P	HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001642	PMID:19206169;PMID:18456719	PCS		10/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002217	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001249	PMID:19206169;PMID:18456719	PCS		17/18			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000176	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002750	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0011968	PMID:18456719	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0009891	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000689	OMIM:115150	TAS					P	HPO:skoehler[2013-07-30]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000325	PMID:18456719	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000962	PMID:19206169	PCS		7/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001597	PMID:18456719	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000540	PMID:18456719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000023	PMID:18456719	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002162	PMID:19206169;PMID:18456719	PCS		8/17			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001909	PMID:18456719	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001508	PMID:19206169	PCS	HP:0003623	14/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001629	PMID:18456719	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000938	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0100625	PMID:18456719	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000657	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000414	PMID:24800029	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002557	PMID:18456719	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000256	PMID:19206169;PMID:18456719	PCS		7/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001744	PMID:18456719	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001622	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002212	PMID:19206169;PMID:18456719;PMID:24800029	PCS		14/20			P	HPO:skoehler[2012-11-16];HPO:probinson[2020-08-10];ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002059	PMID:18456719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001003	PMID:19206169	PCS		5/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0009908	OMIM:115150	TAS					P	HPO:skoehler[2012-11-16]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000391	PMID:18456719	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0005280	PMID:19206169	PCS		16/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001639	PMID:19206169;PMID:24800029	PCS		10/18			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0007333	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001638	PMID:18456719	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0002967	PMID:19206169;PMID:18456719	PCS		10/19			P	ORCID:0000-0002-0736-9199[2025-10-21];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000268	PMID:19206169	PCS		5/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0001631	PMID:19206169	PCS	HP:0003577	3/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-10]
OMIM:115150	Cardiofaciocutaneous syndrome 1		HP:0000545	OMIM:115150	IEA					P	HPO:iea[2009-02-17]
OMIM:143470	Hyperalphalipoproteinemia 1		HP:0012184	PMID:2215607	PCS					P	HPO:probinson[2014-05-24];HPO:probinson[2022-07-03]
OMIM:143470	Hyperalphalipoproteinemia 1		HP:0000006	PMID:2215607	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:145001	Hyperparathyroidism 2		HP:0006735	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0006725	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0010566	OMIM:145001	IEA					P	HPO:skoehler[2010-06-20]
OMIM:145001	Hyperparathyroidism 2		HP:0003072	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0100027	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0006780	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0006781	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0000843	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0002667	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0000113	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0000234	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0000006	OMIM:145001	IEA					I	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0000787	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0006766	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:145001	Hyperparathyroidism 2		HP:0002897	OMIM:145001	IEA					P	HPO:iea[2009-02-17]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0004841	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000486	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0003596	PMID:33964207	PCS		1/7			C	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0011858	PMID:33964207	PCS		4/6			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0003155	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001252	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0002020	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0003593	PMID:33728255;PMID:33964207	PCS		3/8			C	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0012301	PMID:32884905;PMID:33728255;PMID:33964207	PCS		9/9			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0100651	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0012347	PMID:33964207	PCS		7/7			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0012594	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001929	PMID:33964207	PCS		6/6			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001408	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0010296	PMID:32884905;PMID:33964207	PCS		2/8			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0011462	PMID:33964207	PCS		1/7			C	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000316	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001763	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0031956	PMID:32884905;PMID:33728255;PMID:33964207	PCS		8/8			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0030948	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0011889	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0002907	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0008169	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000767	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001976	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000403	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001935	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000768	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000006	PMID:32884905	PCS					I	HPO:probinson[2021-10-28];HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000369	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000324	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000445	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001397	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0003577	PMID:32884905	PCS		1/1			C	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000023	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0002240	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0031964	PMID:32884905;PMID:33728255	PCS		2/2			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000939	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0008151	PMID:32884905;PMID:33728255	PCS		2/2			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001508	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001629	PMID:33964207	PCS		2/7			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001903	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0011120	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0008357	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000774	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0002910	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0006579	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001744	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0003645	PMID:32884905;PMID:33728255	PCS		2/2			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000275	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0003225	PMID:32884905;PMID:33964207	PCS		7/8			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0003621	PMID:33964207	PCS		3/7			C	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0002650	PMID:33728255;PMID:33964207	PCS		4/8			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0031936	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0002013	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000793	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000430	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0011900	PMID:32884905;PMID:33728255	PCS		2/2			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0011069	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0012358	PMID:33964207	PCS		7/7			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0031141	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001636	PMID:33964207	PCS		1/7			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000307	PMID:33728255	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0001873	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0000347	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:619525	Congenital disorder of glycosylation, type IIw		HP:0004502	PMID:32884905	PCS		1/1			P	HPO:probinson[2021-10-28]
OMIM:166800	OTOSCLEROSIS		HP:0000362	OMIM:166800	IEA					P	HPO:iea[2009-02-17]
OMIM:166800	OTOSCLEROSIS		HP:0000405	OMIM:166800	IEA					P	HPO:iea[2009-02-17]
OMIM:166800	OTOSCLEROSIS		HP:0000006	OMIM:166800	IEA					I	HPO:iea[2009-02-17]
OMIM:190600	Triphalangeal thumb, nonopposable		HP:0001199	OMIM:190600	IEA					P	HPO:iea[2009-02-17]
OMIM:190600	Triphalangeal thumb, nonopposable		HP:0010442	OMIM:190600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:190600	Triphalangeal thumb, nonopposable		HP:0000006	OMIM:190600	IEA					I	HPO:iea[2009-02-17]
OMIM:114500	Colorectal cancer		HP:0006716	OMIM:114500	TAS					P	HPO:iea[2012-07-18]
OMIM:114500	Colorectal cancer		HP:0001442	OMIM:114500	IEA					I	HPO:skoehler[2019-02-22]
OMIM:114500	Colorectal cancer		HP:0002891	OMIM:114500	TAS					P	HPO:iea[2009-02-17]
OMIM:114500	Colorectal cancer		HP:0005584	OMIM:114500	TAS					P	HPO:skoehler[2010-06-20]
OMIM:114500	Colorectal cancer		HP:0006740	OMIM:114500	TAS					P	HPO:iea[2009-02-17]
OMIM:114500	Colorectal cancer		HP:0006753	OMIM:114500	TAS					P	HPO:iea[2012-07-18]
OMIM:114500	Colorectal cancer		HP:0000006	OMIM:114500	IEA					I	HPO:skoehler[2019-02-22]
OMIM:163950	Noonan syndrome 1		HP:0001892	PMID:15240615	PCS		3/18			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0000286	PMID:12634870	PCS		15/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0004841	OMIM:163950	IEA					P	HPO:probinson[2012-05-26]
OMIM:163950	Noonan syndrome 1		HP:0002224	PMID:32164556	PCS		9/107			P	HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0001531	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0000365	PMID:15240615	PCS		2/17			P	HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0004322	PMID:15723289	PCS	HP:0003593	41/56			P	HPO:skoehler[2012-11-26];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0004322	PMID:32164556	PCS		43/107			P	HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0000917	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0000958	PMID:32164556	PCS		5/107			P	HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0000914	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0100769	OMIM:163950	TAS					P	HPO:skoehler[2012-11-26]
OMIM:163950	Noonan syndrome 1		HP:0000957	PMID:32164556	PCS		10/107			P	HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0000915	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0000316	PMID:12634870;PMID:32164556	PCS		68/135			P	HPO:probinson[2022-03-31];HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0009466	OMIM:163950	PCS					P	HPO:probinson[2012-03-18]
OMIM:163950	Noonan syndrome 1		HP:0008897	OMIM:163950	PCS					P	HPO:probinson[2012-03-18]
OMIM:163950	Noonan syndrome 1		HP:0001643	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0000476	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0001004	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0001642	PMID:15723289;PMID:32164556;PMID:15240615	PCS		92/181			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];HPO:probinson[2022-03-31];HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0001249	PMID:15240615	PCS		4/17			P	HPO:probinson[2012-03-18];HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0002751	OMIM:163950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163950	Noonan syndrome 1		HP:0000175	PMID:15240615	PCS		1/18			P	HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0000494	PMID:12634870	PCS		19/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0010310	PMID:15240615	PCS		1/18			P	HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0100697	OMIM:163950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163950	Noonan syndrome 1		HP:0000407	OMIM:163950	PCS					P	HPO:probinson[2012-03-18]
OMIM:163950	Noonan syndrome 1		HP:0000766	PMID:15240615	PCS		3/18			P	HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0000689	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0002705	OMIM:163950	TAS					P	HPO:skoehler[2015-12-30]
OMIM:163950	Noonan syndrome 1		HP:0000047	PMID:15240615	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0000006	PMID:11704759	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0000369	PMID:12634870;PMID:32164556	PCS		96/137			P	HPO:probinson[2022-03-31];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0000325	OMIM:163950	PCS					P	HPO:probinson[2012-03-18]
OMIM:163950	Noonan syndrome 1		HP:0001156	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0002162	PMID:12634870;PMID:32164556	PCS		86/138			P	HPO:probinson[2022-03-31];HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0003251	OMIM:163950	TAS					P	HPO:skoehler[2012-11-26]
OMIM:163950	Noonan syndrome 1		HP:0012209	PMID:15240615	PCS		2/18			P	HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0001629	PMID:32164556	PCS	HP:0003577	5/107			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0000337	PMID:32164556	PCS		34/107			P	HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0008872	PMID:15723289	PCS	HP:0003593	35/56			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0004859	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0000978	PMID:15723289	PCS		32/56			P	HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0030084	OMIM:163950	TAS					P	HPO:skoehler[2014-09-21]
OMIM:163950	Noonan syndrome 1		HP:0000218	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0008357	OMIM:163950	TAS					P	HPO:probinson[2009-02-17]
OMIM:163950	Noonan syndrome 1		HP:0006610	PMID:32164556	PCS		37/107			P	HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0000135	OMIM:163950	TAS		HP:0040283			P	HPO:skoehler[2012-11-26]
OMIM:163950	Noonan syndrome 1		HP:0001680	OMIM:163950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163950	Noonan syndrome 1		HP:0000470	PMID:12634870	PCS		15/29			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0001639	PMID:15723289;PMID:32164556;PMID:15240615	PCS		13/181			P	HPO:probinson[2021-05-20];HPO:probinson[2022-03-31];HPO:skoehler[2012-11-26];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0000508	PMID:12634870;PMID:32164556	PCS		77/136			P	HPO:probinson[2022-03-31];HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0002967	PMID:32164556	PCS		13/107			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0001631	PMID:15723289;PMID:32164556;PMID:15240615	PCS	HP:0003577	70/181			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];HPO:probinson[2022-03-31];HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0000465	PMID:12634870	PCS		13/32			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0000465	PMID:12634870	PCS	HP:0003577	10/56			P	HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0000465	PMID:32164556	PCS		65/107			P	HPO:probinson[2022-03-31]
OMIM:163950	Noonan syndrome 1		HP:0000028	PMID:15240615	PCS		5/8			P	HPO:probinson[2021-05-20]
OMIM:163950	Noonan syndrome 1		HP:0000028	PMID:15723289	PCS		27/32	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-12]
OMIM:163950	Noonan syndrome 1		HP:0000347	OMIM:163950	PCS					P	HPO:probinson[2012-03-18]
OMIM:163950	Noonan syndrome 1		HP:0000545	OMIM:163950	IEA					P	HPO:iea[2009-02-17]
OMIM:146520	Hypotrichosis 2		HP:0000164	PMID:12754508	PCS		0/34			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-08]
OMIM:146520	Hypotrichosis 2		HP:0003621	PMID:12754508	PCS		34/34			C	HPO:probinson[2024-03-08]
OMIM:146520	Hypotrichosis 2		HP:0001597	PMID:12754508	PCS		0/34			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-08]
OMIM:146520	Hypotrichosis 2		HP:0002209	PMID:12754508	PCS		34/34			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:146520	Hypotrichosis 2		HP:0000006	PMID:12754508	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0003554	OMIM:159400	IEA					P	HPO:iea[2009-02-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0002664	OMIM:159400	IEA					P	HPO:iea[2009-02-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0003473	OMIM:159400	IEA					P	HPO:iea[2009-02-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0003581	OMIM:159400	IEA					C	HPO:iea[2009-02-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0008180	OMIM:159400	IEA					P	HPO:iea[2009-02-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0100522	OMIM:159400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0000508	OMIM:159400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0007126	OMIM:159400	IEA					P	HPO:iea[2009-02-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0002725	OMIM:159400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0003745	OMIM:159400	IEA					I	HPO:iea[2009-02-17]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0000597	OMIM:159400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0000872	OMIM:159400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:159400	Myasthenia, limb-girdle, autoimmune		HP:0003403	OMIM:159400	IEA					P	HPO:iea[2009-02-17]
OMIM:618613	Retinitis pigmentosa 86		HP:0007737	PMID:30120214	PCS		3/3			P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0000662	PMID:30120214	PCS		3/3			P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0000529	PMID:30120214	PCS		3/3			P	HPO:probinson[2020-06-12];HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0025158	PMID:30120214	PCS					P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0100019	PMID:30120214	PCS		1/3			P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0000007	PMID:30120214	PCS					I	HPO:probinson[2020-06-12];HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0000543	PMID:30120214	PCS		2/3			P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0011505	PMID:30120214	PCS		1/3			P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0007843	PMID:30120214	PCS		3/3			P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0007722	PMID:30120214	PCS		2/3			P	HPO:probinson[2020-06-12]
OMIM:618613	Retinitis pigmentosa 86		HP:0030505	PMID:30120214	PCS		3/3			P	HPO:probinson[2020-06-12]
OMIM:617520	Microcephaly 18, primary, autosomal dominant		HP:0000252	PMID:27008544	PCS		10/10			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2024-03-16]
OMIM:617520	Microcephaly 18, primary, autosomal dominant		HP:0001999	PMID:27008544	PCS		0/10			P	HPO:probinson[2024-03-16]
OMIM:617520	Microcephaly 18, primary, autosomal dominant		HP:0000006	PMID:27008544	PCS					I	HPO:nvasilevsky[2019-02-25];HPO:probinson[2024-03-16]
OMIM:617520	Microcephaly 18, primary, autosomal dominant		HP:0001249	PMID:27008544	PCS		10/10			P	HPO:probinson[2024-03-16]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000286	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0001058	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000460	PMID:30449416	PCS		6/6			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000581	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0010783	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0012785	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0100689	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0100720	PMID:30449416	PCS		2/5			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000678	PMID:30449416	PCS		1/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000218	PMID:30449416	PCS		2/6			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000212	PMID:30449416	PCS		1/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0007502	PMID:30449416	PCS		1/6			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0025616	PMID:30449416	PCS		1/6			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000556	PMID:30449416	PCS		1/3			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000358	PMID:30449416	PCS		3/5			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000413	PMID:30449416	PCS		1/5			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0001386	PMID:30449416	PCS		4/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000430	PMID:30449416	PCS		3/6			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000331	PMID:30449416	PCS		1/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000276	PMID:30449416	PCS		4/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0045025	PMID:30449416	IEA		5/5			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0011800	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0032107	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0009771	PMID:30449416	PCS		3/5			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0011496	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0430007	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0009797	PMID:30449416	PCS		1/5			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0001239	PMID:30449416	PCS		2/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000505	PMID:30449416	PCS		3/4			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000405	PMID:30449416	PCS		2/5			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0006466	PMID:30449416	PCS		1/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0002987	PMID:30449416	PCS		1/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0002107	PMID:30449416	PCS		2/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000963	PMID:30449416	PCS		4/6			P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000369	PMID:30449416	PCS					P	HPO:probinson[2020-06-20]
OMIM:618175	Warburg-Cinotti syndrome		HP:0000006	PMID:30449416	PCS					I	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:194300	Woolly hair, autosomal dominant		HP:0002224	PMID:20346438	PCS		14/14			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0003577	PMID:20346438	PCS					C	HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0032152	PMID:20346438	PCS		0/14			P	HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0002208	PMID:20346438	PCS		14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0000499	PMID:20346438	PCS		0/14			P	HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0000972	PMID:20346438	PCS		0/14			P	HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0002217	PMID:20346438	PCS		14/14			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0000006	PMID:20346438	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0000534	PMID:20346438	PCS		0/14			P	HPO:probinson[2022-12-13]
OMIM:194300	Woolly hair, autosomal dominant		HP:0011359	PMID:20346438	PCS		14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:611637	Primary lateral sclerosis, adult		HP:0002015	OMIM:611637	IEA					P	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0002464	OMIM:611637	IEA					P	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0003487	OMIM:611637	IEA					P	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0001285	OMIM:611637	IEA					P	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0003581	OMIM:611637	TAS					C	HPO:probinson[2012-07-16]
OMIM:611637	Primary lateral sclerosis, adult		HP:0002064	OMIM:611637	IEA					P	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0000006	OMIM:611637	IEA					I	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0003677	OMIM:611637	IEA					C	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0001347	OMIM:611637	IEA					P	HPO:iea[2009-02-17]
OMIM:611637	Primary lateral sclerosis, adult		HP:0002127	OMIM:611637	IEA					P	HPO:iea[2009-02-17]
OMIM:110000	Blepharochalasis, superior		HP:0010749	OMIM:110000	TAS					P	HPO:probinson[2009-02-17]
OMIM:110000	Blepharochalasis, superior		HP:0000006	OMIM:110000	TAS					I	HPO:probinson[2009-02-17]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0010804	PMID:25439098	PCS		1/11			P	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000486	PMID:25439098	PCS		3/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0002540	PMID:25439098	PCS		1/8			P	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0002188	PMID:25439098	PCS		4/11			P	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000463	PMID:25439098	PCS		1/11			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0001250	PMID:25439098	PCS		9/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0001252	PMID:25439098	PCS	HP:0003623	11/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0003593	PMID:25439098	PCS		2/7			C	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000639	PMID:25439098	PCS		4/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0011463	PMID:25439098	PCS		2/7			C	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0011220	OMIM:616158	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000637	PMID:25439098	PCS		1/11			P	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0003429	PMID:25439098	PCS		4/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000218	PMID:25439098	PCS		3/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0001249	PMID:25439098	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0003623	PMID:25439098	PCS		3/7			C	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0002058	PMID:25439098	PCS		6/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0002136	OMIM:616158	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0001344	PMID:25439098	PCS		8/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000431	PMID:25439098	PCS		1/11			P	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000430	PMID:25439098	PCS		1/11			P	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0011968	PMID:25439098	PCS		11/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000194	PMID:25439098	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0001263	PMID:25439098	PCS		11/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0002093	PMID:25439098	PCS		10/10			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000506	OMIM:616158	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0001319	OMIM:616158	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000565	PMID:25439098	PCS		1/11			P	HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0000006	PMID:25439098	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:616158	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties		HP:0001336	PMID:25439098	PCS	HP:0003593				P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0200073	PMID:23849778	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0012265	PMID:23849778	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0002257	PMID:23849778	PCS		5/12			P	HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0001696	PMID:23849778	PCS		8/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0002110	PMID:23849778	PCS		7/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0000403	PMID:23849778	PCS		4/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0000007	PMID:23849778	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0031245	PMID:23849778	PCS		8/12		HP:0011010	P	HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0006532	PMID:23849778	PCS		5/12			P	HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0011108	PMID:23849778	PCS		7/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0002643	PMID:23849778	PCS	HP:0003623	5/12			P	HPO:probinson[2021-05-09]
OMIM:615451	Ciliary dyskinesia, primary, 23		HP:0004469	PMID:23849778	PCS		7/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2021-05-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0005387	OMIM:312863	TAS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0003593	PMID:9399950	PCS		1/1			C	HPO:probinson[2024-03-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0011839	PMID:9399950	PCS		0/1			P	HPO:probinson[2024-03-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0002090	OMIM:312863	IEA					P	HPO:iea[2009-02-17]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0010975	PMID:9399950	PCS		0/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0001419	PMID:8462096	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-03-19]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0040089	PMID:9399950	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2019-03-19];HPO:probinson[2024-03-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0002837	OMIM:312863	IEA					P	HPO:iea[2009-02-17]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0020102	PMID:9399950	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0000246	OMIM:312863	IEA					P	HPO:iea[2009-02-17]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0000388	OMIM:312863	IEA					P	HPO:iea[2009-02-17]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0004315	PMID:9399950	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:312863	Combined immunodeficiency, X-linked		HP:0005415	OMIM:312863	IEA					P	HPO:iea[2009-02-17]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0003456	OMIM:603233	IEA					P	HPO:iea[2009-02-17]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0001156	OMIM:603233	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0003165	OMIM:603233	IEA					P	HPO:iea[2009-02-17]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0002905	OMIM:603233	IEA					P	HPO:iea[2009-02-17]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0010049	OMIM:603233	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0002901	OMIM:603233	IEA					P	HPO:iea[2009-02-17]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0003745	OMIM:603233	IEA					I	HPO:iea[2009-02-17]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0000006	PMID:11406605	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-04-25]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0001513	OMIM:603233	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:603233	Pseudohypoparathyroidism, type IB		HP:0000852	OMIM:603233	IEA					P	HPO:iea[2009-02-17]
OMIM:271320	Spinocerebellar degeneration with macular corneal dystrophy, congenitalcataracts, and myopia		HP:0002497	OMIM:271320	IEA					P	HPO:iea[2009-02-17]
OMIM:271320	Spinocerebellar degeneration with macular corneal dystrophy, congenitalcataracts, and myopia		HP:0001131	OMIM:271320	IEA					P	HPO:skoehler[2010-06-20]
OMIM:271320	Spinocerebellar degeneration with macular corneal dystrophy, congenitalcataracts, and myopia		HP:0000519	OMIM:271320	IEA					P	HPO:iea[2009-02-17]
OMIM:271320	Spinocerebellar degeneration with macular corneal dystrophy, congenitalcataracts, and myopia		HP:0000007	OMIM:271320	IEA					I	HPO:iea[2009-02-17]
OMIM:271320	Spinocerebellar degeneration with macular corneal dystrophy, congenitalcataracts, and myopia		HP:0002503	OMIM:271320	IEA					P	HPO:iea[2009-02-17]
OMIM:271320	Spinocerebellar degeneration with macular corneal dystrophy, congenitalcataracts, and myopia		HP:0000545	OMIM:271320	IEA					P	HPO:skoehler[2010-06-20]
OMIM:618161	Joubert syndrome 35		HP:0000662	PMID:30269812	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000463	PMID:30269812	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0001251	PMID:30269812	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0001290	PMID:30269812	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0011933	PMID:30269812	PCS		4/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000657	PMID:30269812	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000954	PMID:30269812	PCS		1/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0002419	PMID:30269812	PCS		4/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000510	PMID:30269812	PCS		4/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0001320	PMID:30269812	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0002553	PMID:30269812	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000010	PMID:30269812	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0001263	PMID:30269812	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0030760	PMID:30269812	PCS		1/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0004370	PMID:30269812	PCS		2/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0005280	PMID:30269812	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0010535	PMID:30269812	PCS		1/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000529	PMID:30269812	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000506	PMID:30269812	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000508	PMID:30269812	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000007	PMID:30269812	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000768	PMID:30269812	PCS		1/4			P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000664	PMID:30269812	PCS					P	HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000003	PMID:30269812	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000369	PMID:30269812	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-14]
OMIM:618161	Joubert syndrome 35		HP:0000126	PMID:30269812	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:617252	Uncombable hair syndrome 3		HP:0002212	PMID:27866708	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:617252	Uncombable hair syndrome 3		HP:0002235	PMID:27866708	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617252	Uncombable hair syndrome 3		HP:0002299	PMID:27866708	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:617252	Uncombable hair syndrome 3		HP:0011463	PMID:27866708	PCS		1/1			C	HPO:probinson[2023-02-04]
OMIM:617252	Uncombable hair syndrome 3		HP:0030056	PMID:27866708	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617252	Uncombable hair syndrome 3		HP:0000007	PMID:27866708	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:608372	Deafness, autosomal dominant nonsyndromic sensorineural 49		HP:0003621	OMIM:608372	IEA					C	HPO:iea[2009-02-17]
OMIM:608372	Deafness, autosomal dominant nonsyndromic sensorineural 49		HP:0000407	OMIM:608372	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608372	Deafness, autosomal dominant nonsyndromic sensorineural 49		HP:0001730	OMIM:608372	IEA					P	HPO:iea[2009-02-17]
OMIM:608372	Deafness, autosomal dominant nonsyndromic sensorineural 49		HP:0000006	OMIM:608372	IEA					I	HPO:iea[2009-02-17]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0003596	PMID:33889941	PCS		1/4			C	HPO:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0003693	PMID:33889941	PCS		2/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0003394	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0003593	PMID:33889941	PCS		1/4			C	HPO:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0033466	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0031189	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0030319	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0011463	PMID:33889941	PCS		2/4			C	HPO:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0009027	PMID:33889941	PCS		3/4			P	HP:probinson[2021-10-26];HPO:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0009005	PMID:33889941	PCS		2/4			P	HP:probinson[2021-10-26];HPO:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0002936	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0007149	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0001643	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0001763	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0001348	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0002650	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0031936	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0008959	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0001284	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0033383	PMID:33889941	PCS		1/1			P	HP:probinson[2021-10-26];HPO:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0009830	PMID:33889941	PCS		4/4			P	HP:probinson[2021-10-26];HPO:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0001239	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0003438	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0006886	PMID:33889941	PCS		3/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0000006	PMID:33889941	PCS					I	HPO:probinson[2021-10-24];HPO:probinson[2021-10-24]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0008944	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:619519	Charcot-Marie-Tooth disease, axonal, type 2FF		HP:0001611	PMID:33889941	PCS		1/4			P	HP:probinson[2021-10-26]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0003027	OMIM:601356	IEA					P	HPO:iea[2009-02-17]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0007759	OMIM:601356	IEA					P	HPO:iea[2009-02-17]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0009826	OMIM:601356	TAS				HP:0012828	P	HPO:probinson[2012-05-05]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0005720	OMIM:601356	TAS					P	HPO:probinson[2012-06-03]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0000260	OMIM:601356	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0011910	OMIM:601356	TAS					P	HPO:probinson[2012-06-03]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0000926	OMIM:601356	IEA					P	HPO:iea[2009-02-17]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0000007	OMIM:601356	IEA					I	HPO:iea[2009-02-17]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0005716	OMIM:601356	TAS					P	HPO:probinson[2009-02-17]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0002645	OMIM:601356	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0000256	OMIM:601356	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0000413	OMIM:601356	IEA					P	HPO:iea[2009-02-17]
OMIM:601356	Lethal short-limb skeletal dysplasia, al Gazali type		HP:0001776	OMIM:601356	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000286	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0008749	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0004325	OMIM:182210	TAS					P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0002023	OMIM:182210	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0004322	OMIM:182210	TAS					P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0001195	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0002000	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0001252	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0001290	OMIM:182210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0002938	OMIM:182210	TAS					P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0001328	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000774	OMIM:182210	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000454	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0001620	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000153	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0002650	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000233	OMIM:182210	TAS					P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000431	OMIM:182210	TAS					P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0002808	OMIM:182210	TAS					P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0001999	OMIM:182210	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0009555	OMIM:182210	TAS					P	HPO:probinson[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0001539	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0005956	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000465	OMIM:182210	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0000006	OMIM:182210	IEA					I	HPO:iea[2009-02-17]
OMIM:182210	Shprintzen omphalocele syndrome		HP:0002643	OMIM:182210	IEA					P	HPO:iea[2009-02-17]
OMIM:620398	Glycine encephalopathy 2		HP:0500230	PMID:9600239	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0001250	PMID:9600239	PCS	HP:0003623	14/14			P	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0011463	PMID:8005589	PCS		1/1			C	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0011342	PMID:8005589	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0008288	PMID:8005589;PMID:9600239	PCS		16/16			P	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0000007	PMID:8005589	PCS					I	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0010851	PMID:9600239	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0002878	PMID:9600239	PCS	HP:0003623	14/14			P	HPO:probinson[2023-07-08]
OMIM:620398	Glycine encephalopathy 2		HP:0003623	PMID:9600239	PCS		14/14			C	HPO:probinson[2023-07-08]
OMIM:227600	Factor X deficiency		HP:0000132	OMIM:227600	IEA					P	HPO:iea[2009-02-17]
OMIM:227600	Factor X deficiency		HP:0012233	OMIM:227600	TAS					P	HPO:skoehler[2013-05-31]
OMIM:227600	Factor X deficiency		HP:0008151	PMID:2790181	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-16]
OMIM:227600	Factor X deficiency		HP:0008321	PMID:2790181	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:227600	Factor X deficiency		HP:0000007	PMID:2790181	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:227600	Factor X deficiency		HP:0005261	OMIM:227600	IEA					P	HPO:iea[2009-02-17]
OMIM:227600	Factor X deficiency		HP:0002170	OMIM:227600	IEA					P	HPO:iea[2009-02-17]
OMIM:227600	Factor X deficiency		HP:0004846	PMID:2790181	PCS		1/1			P	HPO:probinson[2023-01-16]
OMIM:227600	Factor X deficiency		HP:0000421	OMIM:227600	IEA					P	HPO:iea[2009-02-17]
OMIM:227600	Factor X deficiency		HP:0000225	OMIM:227600	TAS					P	HPO:probinson[2009-02-17]
OMIM:227600	Factor X deficiency		HP:0003645	OMIM:227600	TAS					P	HPO:probinson[2012-06-02]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0003235	PMID:15024124	PCS		1/1			P	HPO:probinson[2012-07-16];HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0002421	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0000164	OMIM:613752	TAS					P	HPO:probinson[2012-07-16]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0031956	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0001263	PMID:15024124	PCS		1/1			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0001252	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0003593	PMID:15024124	PCS		1/1			C	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:6000750	PMID:15024124	PCS		1/1			P	HPO:probinson[2024-06-29]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0003073	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0032234	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0001270	OMIM:613752	TAS					P	HPO:probinson[2012-07-16]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0031964	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0001508	OMIM:613752	TAS					P	HPO:probinson[2012-07-16]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0031143	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0001999	OMIM:613752	TAS					P	HPO:probinson[2012-07-16]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0000007	PMID:15024124	PCS					I	HPO:probinson[2012-07-16];HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0020045	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0001638	OMIM:613752	TAS					P	HPO:probinson[2012-07-16]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0001249	OMIM:613752	TAS					P	HPO:probinson[2012-07-16]
OMIM:613752	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase		HP:0003557	PMID:15024124	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000286	PMID:25810209	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000486	PMID:25810209	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0004322	PMID:25810209	PCS		5/5			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001250	PMID:25810209;OMIM:605130	PCS		10/15			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-11-18];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002263	PMID:25810209;PMID:22795537	PCS		6/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001252	PMID:25810209	PCS		2/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0012745	PMID:25810209;PMID:22795537	PCS		1/10			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0031623	PMID:25810209	PCS		2/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0011463	PMID:36291481	PCS		1/1			C	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0011220	PMID:25810209	PCS		3/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000718	PMID:25810209;PMID:22795537	PCS		3/11			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000717	PMID:25810209;PMID:22795537	PCS		2/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000316	PMID:25810209	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000437	PMID:25810209	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0008897	PMID:25810209;PMID:36291481	PCS		6/6			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000637	PMID:25810209	PCS		2/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001847	PMID:25810209;PMID:22795537	PCS		3/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001643	PMID:22795537	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000752	PMID:25810209;PMID:22795537	PCS		2/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001763	PMID:36291481	PCS		1/1			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002019	PMID:25810209;PMID:22795537	PCS		6/11			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-11-18];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001249	PMID:25810209;PMID:36291481	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002553	PMID:25810209;PMID:36291481	PCS		4/6			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000252	PMID:25810209	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000494	PMID:25810209;PMID:22795537;PMID:36291481	PCS		10/12			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-11-20];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000574	PMID:25810209;PMID:22795537;PMID:36291481	PCS		11/12			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002750	OMIM:605130	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001382	PMID:25810209	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002230	PMID:25810209	PCS		5/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0011968	PMID:25810209;PMID:22795537	PCS		5/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001263	PMID:25810209;PMID:22795537	PCS		11/11			P	HPO:probinson[2023-02-10];HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0004691	PMID:25810209;PMID:22795537	PCS		4/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001182	PMID:25810209;PMID:22795537	PCS		6/11			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-11-18];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0011298	PMID:25810209	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0005819	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000403	PMID:25810209	PCS		1/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0009697	PMID:25810209	PCS		2/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000527	PMID:25810209;PMID:22795537;PMID:36291481	PCS		11/12			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-11-18];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0004209	PMID:25810209	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0005616	PMID:25810209	PCS		0/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000960	PMID:25810209;PMID:22795537	PCS		6/10			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-11-18];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000369	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000006	PMID:22795537	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000445	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000343	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002000	PMID:25810209	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002360	PMID:25810209;PMID:22795537	PCS		4/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002162	PMID:25810209;PMID:36291481	PCS		4/6			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000581	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0004780	PMID:25810209;PMID:22795537;PMID:36291481	PCS		10/12			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0012368	OMIM:605130	TAS					P	HPO:skoehler[2013-10-22]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001508	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000414	PMID:36291481	PCS		1/1			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000219	PMID:25810209;PMID:22795537	PCS		7/11			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000218	PMID:25810209	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000455	PMID:25810209;PMID:22795537;PMID:36291481	PCS		9/12			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0009803	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002136	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000431	PMID:25810209;PMID:22795537	PCS		9/11			P	HPO:probinson[2023-02-10];HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0002650	PMID:25810209;PMID:22795537	PCS		1/11			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0004554	PMID:36291481	PCS		1/1			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000750	PMID:36291481	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000592	PMID:25810209	PCS		3/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0045025	PMID:25810209;PMID:22795537	PCS		8/11			P	HPO:probinson[2023-02-10];HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0100874	PMID:25810209;PMID:36291481	PCS		4/5			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000668	PMID:25810209	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0009237	PMID:25810209	PCS		2/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000664	PMID:36291481	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0200055	PMID:25810209	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001511	PMID:25810209	PCS		3/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0007655	PMID:25810209	PCS		2/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001631	PMID:22795537	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000347	PMID:25810209	PCS		3/5			P	HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0000028	PMID:25810209;PMID:36291481	PCS		1/4			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0001831	OMIM:605130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605130	Wiedemann-Steiner syndrome		HP:0007933	PMID:25810209;PMID:22795537	PCS		4/11			P	HPO:probinson[2023-07-01]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001320	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000341	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000486	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000574	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001344	OMIM:616819	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000463	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000232	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001321	OMIM:616819	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001263	OMIM:616819	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000294	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001251	OMIM:616819	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0012724	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0008070	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0007370	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0011451	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000007	PMID:25388005	PCS					I	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001338	OMIM:616819	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000527	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000411	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001007	PMID:25388005	PCS					P	HPO:probinson[2017-06-17]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000369	OMIM:616819	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0000358	OMIM:616819	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		HP:0001249	OMIM:616819	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0002102	PMID:9843983	PCS		53/220	FEMALE		P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0000077	PMID:16642431	PCS		32.3%			P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0000992	PMID:16642431	PCS		76.3%			P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0005268	PMID:9843983	PCS		13/220	FEMALE		C	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0003493	PMID:9843983	PCS		98/220	FEMALE		P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0025300	PMID:16642431	PCS		66%	FEMALE		P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0010982	OMIM:609939	TAS			FEMALE		I	HPO:probinson[2013-03-31]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0012211	PMID:9843983	PCS		30/220	FEMALE		P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0000707	PMID:16642431	PCS		24.3%			P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0002715	PMID:16642431	PCS		56.6%			P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0001701	PMID:9843983	PCS		18/220	FEMALE		P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0002725	PMID:9843983	PCS		76.3%	FEMALE		P	HPO:probinson[2013-01-09]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0001369	PMID:9843983	PCS		85/220	FEMALE		P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0001369	PMID:9843983	PCS		78.3%			P	HPO:lccarmody[2018-06-19]
OMIM:609939	Systemic lupus erythematosus, susceptibility to, 6		HP:0000951	PMID:9843983	PCS		91/220	FEMALE		P	HPO:lccarmody[2018-06-19]
OMIM:137440	Gerstmann-Straussler disease		HP:0002067	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0001272	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0002186	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0002066	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0002063	OMIM:137440	TAS					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0002185	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0000716	OMIM:137440	TAS					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0007340	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0000718	OMIM:137440	TAS					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0000712	OMIM:137440	TAS					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0001824	OMIM:137440	TAS					P	HPO:skoehler[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0000751	OMIM:137440	TAS					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0001347	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0001300	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0002078	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0002354	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0030223	OMIM:137440	TAS					P	HPO:skoehler[2015-01-04]
OMIM:137440	Gerstmann-Straussler disease		HP:0001260	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0003581	OMIM:137440	TAS					C	HPO:skoehler[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0001284	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0002070	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0000709	OMIM:137440	TAS					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0000726	OMIM:137440	TAS	HP:0003584				P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0007772	OMIM:137440	IEA					P	HPO:skoehler[2010-06-18]
OMIM:137440	Gerstmann-Straussler disease		HP:0001257	OMIM:137440	TAS					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0000006	OMIM:137440	TAS					I	HPO:probinson[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0001337	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0001336	OMIM:137440	IEA					P	HPO:iea[2009-02-17]
OMIM:137440	Gerstmann-Straussler disease		HP:0003678	OMIM:137440	TAS					C	HPO:skoehler[2009-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0002224	PMID:36689522	PCS		9/9			P	HPO:probinson[2024-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0003577	PMID:36689522	PCS		7/9			C	HPO:probinson[2024-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0001030	PMID:36689522	PCS		8/9			P	HPO:probinson[2024-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0032152	PMID:36689522	PCS		6/9			P	HPO:probinson[2024-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0003593	PMID:36689522	PCS		2/9			C	HPO:probinson[2024-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0000007	PMID:36689522	PCS					I	HPO:probinson[2024-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0000982	PMID:36689522	PCS		0/9			P	HPO:probinson[2024-02-17]
OMIM:620415	Woolly hair-skin fragility syndrome		HP:0100792	PMID:36689522	PCS		2/2			P	HPO:probinson[2024-02-17]
OMIM:125050	Deafness with anhidrotic ectodermal dysplasia		HP:0007476	OMIM:125050	TAS					P	HPO:probinson[2009-02-17]
OMIM:125050	Deafness with anhidrotic ectodermal dysplasia		HP:0001730	OMIM:125050	TAS					P	HPO:probinson[2009-02-17]
OMIM:125050	Deafness with anhidrotic ectodermal dysplasia		HP:0000006	OMIM:125050	TAS					I	HPO:probinson[2009-02-17]
OMIM:611804	Elliptocytosis 1		HP:0004445	PMID:3058231	PCS					P	HPO:skoehler[2013-01-09]
OMIM:611804	Elliptocytosis 1		HP:0000980	OMIM:611804	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611804	Elliptocytosis 1		HP:0001878	PMID:3058231	PCS					P	HPO:skoehler[2013-04-02]
OMIM:611804	Elliptocytosis 1		HP:0000007	OMIM:611804	IEA					I	HPO:skoehler[2018-10-08]
OMIM:611804	Elliptocytosis 1		HP:0000006	PMID:3058231	PCS					I	HPO:skoehler[2013-04-02]
OMIM:611804	Elliptocytosis 1		HP:0000952	OMIM:611804	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611804	Elliptocytosis 1		HP:0001744	OMIM:611804	IEA					P	HPO:skoehler[2019-04-18]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0001399	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0003596	PMID:35420632	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0030169	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0002094	PMID:35420632	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0002040	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0011954	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0031950	PMID:35420632	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0001082	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0031246	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0031413	PMID:35420632	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0031996	PMID:35420632	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0045051	PMID:35420632	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0001409	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0011462	PMID:35420632	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0001217	PMID:35420632	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0005518	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0002216	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0001873	PMID:35420632	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0002206	PMID:35420632	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0001744	PMID:35420632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620367	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8		HP:0000006	PMID:35420632	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156900	Microphthalmia, isolated, with corectopia		HP:0009918	OMIM:156900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:156900	Microphthalmia, isolated, with corectopia		HP:0000568	OMIM:156900	IEA					P	HPO:iea[2009-02-17]
OMIM:156900	Microphthalmia, isolated, with corectopia		HP:0000006	OMIM:156900	IEA					I	HPO:iea[2009-02-17]
OMIM:156900	Microphthalmia, isolated, with corectopia		HP:0000545	OMIM:156900	IEA					P	HPO:iea[2009-02-17]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000286	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0001331	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000582	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000483	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0006989	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000343	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000486	PMID:31883643	PCS		2/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000540	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0005235	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0003196	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0001274	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000041	PMID:31883643	PCS		2/4	MALE		P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0012745	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0002282	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0030716	PMID:31883643	PCS	HP:0011461	1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0010464	PMID:31883643	PCS		2/8	FEMALE		P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0012368	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0010941	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000316	PMID:31883643	PCS		2/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000537	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000411	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000356	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000256	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0002751	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000054	PMID:31883643	PCS		1/4	MALE		P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000276	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000133	PMID:31883643	PCS					P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0003762	PMID:31883643	PCS		1/8	FEMALE		P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0001387	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0030048	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0001360	PMID:31883643	PCS		2/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0001263	PMID:31883643	PCS		7/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0005484	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0011102	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000508	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0100779	PMID:31883643	PCS		2/8	FEMALE		P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0002308	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000505	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0001539	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0008665	PMID:31883643	PCS		1/8	FEMALE		P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0001159	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000047	PMID:31883643	PCS		4/4			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0007018	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000006	PMID:31883643	PCS					I	HPO:probinson[2020-06-11];HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000347	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000369	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0000028	PMID:31883643	PCS		3/4	MALE		P	HPO:probinson[2020-06-11]
OMIM:618820	Genitourinary and/or/brain malformation syndrome		HP:0002126	PMID:31883643	PCS		1/12			P	HPO:probinson[2020-06-11]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0002344	OMIM:169500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0003676	OMIM:169500	IEA					C	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0001251	PMID:21225301	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0007480	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0000716	OMIM:169500	TAS					P	HPO:skoehler[2015-12-30]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0000639	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0007262	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0007024	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0008652	PMID:21225301	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0006994	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0002415	PMID:21225301	PCS		6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0000751	OMIM:169500	TAS					P	HPO:skoehler[2013-11-18]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0002019	PMID:21225301	PCS		4/6			P	HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0001347	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0003487	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0003581	PMID:21225301	PCS					C	HPO:probinson[2009-02-17];HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0005341	PMID:21225301	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0002171	OMIM:169500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0007371	OMIM:169500	TAS					P	HPO:skoehler[2013-11-18]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0002607	PMID:21225301	PCS		1/6			P	HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0001317	OMIM:169500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0004926	PMID:21225301	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0000802	PMID:21225301	PCS			MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2021-03-25]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0001257	OMIM:169500	IEA					P	HPO:iea[2009-02-17]
OMIM:169500	Leukodystrophy, adult-onset, autosomal dominant		HP:0000006	OMIM:169500	IEA					I	HPO:iea[2009-02-17]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0002311	PMID:31047799	PCS		2/2			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0000252	PMID:29302074	PCS		1/3			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0031936	PMID:31047799	PCS		2/2			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0001250	PMID:29302074	PCS		1/3			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0002286	PMID:29302074	PCS		2/3			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0002066	PMID:31047799	IEA		2/2			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0001260	PMID:31047799	PCS		2/2			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0003141	PMID:31047799	PCS		2/2			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0011342	PMID:29302074	PCS		3/3			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0000718	PMID:31047799	PCS		1/2			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0000519	PMID:29302074	PCS	HP:0003577	1/3			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0000007	PMID:29302074	PCS					I	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0001324	PMID:29302074	PCS		1/3			P	HPO:probinson[2020-05-12]
OMIM:618808	Intellectual developmental disorder with poor growth and with or without seizures or ataxia		HP:0001249	PMID:29302074	PCS					P	HPO:probinson[2020-05-12]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0001265	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0000153	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0002015	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0003236	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0000144	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0000771	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0001283	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0001260	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0003394	OMIM:313200	TAS					P	HPO:probinson[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0003581	OMIM:313200	TAS					C	HPO:probinson[2012-07-16]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0002380	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0003690	OMIM:313200	TAS					P	HPO:probinson[2012-07-16]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0001419	OMIM:313200	IEA					I	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0008981	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0009830	OMIM:313200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0000029	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0000763	OMIM:313200	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0001337	OMIM:313200	IEA					P	HPO:iea[2009-02-17]
OMIM:313200	Spinal and bulbar muscular atrophy, X-linked 1		HP:0003677	OMIM:313200	IEA					C	HPO:iea[2009-02-17]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0011709	OMIM:614954	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0005301	OMIM:614954	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0005110	OMIM:614954	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0001636	OMIM:614954	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0011712	OMIM:614954	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0001627	OMIM:614954	IEA					P	HPO:skoehler[2015-12-30]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0001649	OMIM:614954	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0001631	OMIM:614954	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0000006	OMIM:614954	TAS					I	HPO:skoehler[2015-12-30]
OMIM:614954	Congenital heart defects, multiple types, 3		HP:0001678	OMIM:614954	IEA					P	HPO:skoehler[2018-10-08]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0025143	PMID:10741953	PCS				HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0001025	PMID:31777803	PCS		1/1		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0000365	PMID:31777803	PCS		0/1			P	HPO:probinson[2020-09-26];HPO:probinson[2022-12-03]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0003593	PMID:10741953	PCS					C	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0012378	PMID:10741953	PCS				HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0011227	PMID:31777803;PMID:10741953	PCS		11/11		HP:0025206;HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0002829	PMID:31777803;PMID:10741953	PCS		11/11		HP:0025206;HP:0025206	P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0000509	PMID:31777803;PMID:11687797	PCS		11/11		HP:0025206;HP:0025206	P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0001917	PMID:10741953	PCS	HP:0003584	1/26			P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0032154	PMID:31777803	PCS		1/1		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0001954	PMID:11687797	PCS				HP:0025206	P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0000988	PMID:11687797	PCS				HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0001945	PMID:31777803	IEA		1/1		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0002315	PMID:10741953	PCS				HP:0025206	P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0000554	PMID:31777803	PCS		1/1		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0000006	PMID:11687797	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0001974	PMID:10741953	PCS				HP:0025206	P	HPO:skoehler[2010-06-20];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0003326	PMID:10741953	PCS				HP:0025206	P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-26]
OMIM:120100	Familial cold inflammatory syndrome 1		HP:0001369	PMID:31777803	PCS		1/1		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0000640	PMID:25808372	PCS		17/17			P	HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001310	PMID:25808372	PCS		17/17			P	HPO:skoehler[2012-10-17]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0004322	PMID:25808372	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0002066	PMID:25808372	PCS		17/17			P	HPO:skoehler[2017-07-13]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001252	PMID:25808372	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001251	OMIM:213200	TAS	HP:0003577				P	HPO:probinson[2009-02-17]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0003593	OMIM:213200;PMID:25808372	PCS		27/27			C	HPO:probinson[2023-02-11];HPO:skoehler[2012-10-17]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001152	PMID:25808372	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001290	OMIM:213200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0000639	OMIM:213200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0002317	OMIM:213200	TAS					P	HPO:probinson[2009-02-17]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001249	PMID:25808372	PCS		15/17			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001347	PMID:25808372	PCS		11/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0006855	PMID:25808372	PCS					P	HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001265	OMIM:213200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0002311	OMIM:213200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0000750	PMID:25808372	PCS		14/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001321	OMIM:213200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001761	OMIM:213200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0031936	PMID:25808372	PCS		16/16			P	HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001260	PMID:25808372	PCS		17/17			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0002198	PMID:25808372	PCS					P	HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001263	PMID:25808372	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0003680	OMIM:213200	TAS					C	HPO:skoehler[2012-10-17]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0002171	OMIM:213200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0002070	OMIM:213200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0000007	PMID:25808372	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001257	PMID:25808372	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2		HP:0001337	OMIM:213200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615486	Interstitial lung and liver disease		HP:0001397	PMID:24103465;PMID:25913036	PCS		6/30			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0003676	OMIM:615486	TAS					C	HPO:skoehler[2015-12-30]
OMIM:615486	Interstitial lung and liver disease		HP:0001396	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001894	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001399	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0003355	PMID:24103465	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001252	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001395	PMID:25913036	PCS		1/29			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0003593	PMID:25913036	PCS		26/29			C	HPO:probinson[2021-10-10];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0002240	PMID:25913036	PCS		25/29			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001394	PMID:25913036	PCS		8/29			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001270	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0031964	PMID:25913036	PCS		13/29			P	HPO:probinson[2021-10-10];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001508	PMID:24103465;PMID:25913036	PCS		23/30			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0011463	PMID:25913036	PCS		3/29			C	HPO:probinson[2021-10-10];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001903	PMID:24103465	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001987	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0006530	PMID:24103465	PCS		1/1			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0003623	PMID:24103465	PCS		1/1			C	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0003128	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0031956	PMID:25913036	PCS		19/29			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0006517	PMID:25913036	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0002013	PMID:24103465	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0002094	PMID:25913036	PCS		28/29			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0012735	PMID:25913036	PCS		7/29			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0030948	PMID:25913036	PCS		20/29			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0002093	PMID:25913036	PCS					P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0012418	PMID:25913036	PCS		14/29			P	HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0000821	PMID:24103465	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0001217	PMID:25913036	PCS		8/29			P	HPO:skoehler[2015-07-05];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0000007	PMID:24103465	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-10]
OMIM:615486	Interstitial lung and liver disease		HP:0002206	PMID:25913036	PCS		12/18			P	HPO:probinson[2021-10-10]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0000970	OMIM:614940	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0002298	OMIM:614940	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0007607	PMID:26440664	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-12]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0000232	OMIM:614940	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0002299	PMID:26440664	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0000958	OMIM:614940	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0002561	OMIM:614940	IEA		HP:0040283			P	HPO:skoehler[2013-01-11]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0000668	OMIM:614940	TAS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0000966	PMID:26440664	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0000006	PMID:17354266	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2023-02-12]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0008070	PMID:26440664	PCS		3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-02-12]
OMIM:614940	Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant		HP:0000677	PMID:21626677	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:613949	Okt4 epitope deficiency		HP:0002843	OMIM:613949	IEA					P	HPO:skoehler[2015-08-23]
OMIM:217700	Corneal endothelial dystrophy, autosomal recessive		HP:0007759	PMID:16767101	PCS	HP:0003577				P	HPO:iea[2009-02-17];HPO:probinson[2020-09-08]
OMIM:217700	Corneal endothelial dystrophy, autosomal recessive		HP:0011490	PMID:16767101	PCS					P	HPO:probinson[2020-09-08]
OMIM:217700	Corneal endothelial dystrophy, autosomal recessive		HP:0001131	PMID:16767101	PCS	HP:0003577				P	HPO:probinson[2022-09-05]
OMIM:217700	Corneal endothelial dystrophy, autosomal recessive		HP:0000007	PMID:16767101	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-08]
OMIM:217700	Corneal endothelial dystrophy, autosomal recessive		HP:0011487	PMID:16767101	PCS					P	HPO:probinson[2020-09-08]
OMIM:613791	Masp2 deficiency		HP:0100279	PMID:12904520	PCS		1/1			P	HPO:probinson[2015-03-28]
OMIM:613791	Masp2 deficiency		HP:0004431	PMID:12904520	PCS		1/1			P	HPO:probinson[2015-03-28]
OMIM:613791	Masp2 deficiency		HP:0000007	OMIM:613791	TAS					I	HPO:skoehler[2017-07-13]
OMIM:613791	Masp2 deficiency		HP:0002725	PMID:12904520	PCS		1/1			P	HPO:probinson[2015-03-28]
OMIM:613791	Masp2 deficiency		HP:0006532	PMID:12904520	PCS		1/1			P	HPO:probinson[2015-03-28]
OMIM:616831	Luscan-Lumish syndrome		HP:0004322	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0001250	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0003396	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0001350	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0001290	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0100962	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000858	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000718	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0011220	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000739	OMIM:616831	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616831	Luscan-Lumish syndrome		HP:0001548	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0002119	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000256	OMIM:616831	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616831	Luscan-Lumish syndrome		HP:0001007	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0001249	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0000494	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0003189	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000750	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000276	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0004233	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0002591	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0001263	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0000272	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0009890	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000729	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0002308	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0001833	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000348	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000403	OMIM:616831	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616831	Luscan-Lumish syndrome		HP:0000307	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000147	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000006	PMID:24852293	PCS					I	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0001513	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:616831	Luscan-Lumish syndrome		HP:0000303	PMID:24852293	PCS					P	HPO:probinson[2017-06-17]
OMIM:247650	Lymphokine deficiency		HP:0001939	OMIM:247650	IEA					P	HPO:iea[2009-02-17]
OMIM:247650	Lymphokine deficiency		HP:0002728	OMIM:247650	IEA					P	HPO:iea[2009-02-17]
OMIM:247650	Lymphokine deficiency		HP:0000007	OMIM:247650	IEA					I	HPO:iea[2009-02-17]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002223	PMID:26991760	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000561	PMID:26991760	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000970	OMIM:614941	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000232	OMIM:614941	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002231	OMIM:614941	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002561	OMIM:614941	IEA		HP:0040283			P	HPO:skoehler[2013-01-11]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0005280	OMIM:614941	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0008070	OMIM:614941	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000958	PMID:26991760	PCS		2/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000968	OMIM:614941	IEA		HP:0040280			P	HPO:skoehler[2013-01-09]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0012384	PMID:26991760	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000607	OMIM:614941	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000217	PMID:26991760	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002209	PMID:26991760	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000668	PMID:26991760;OMIM:614941	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000007	PMID:11780064	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000653	OMIM:614941	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002205	PMID:26991760	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002557	OMIM:614941	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0005338	OMIM:614941	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614941	Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000698	OMIM:614941	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0001276	PMID:27912044	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0002465	PMID:27912044	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0002069	PMID:27912044	PCS		5/7			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0000582	PMID:27912044	PCS		1/4			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0000343	PMID:27912044	PCS		1/4			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0001252	PMID:27912044	PCS		1/7			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0003593	PMID:27912044	PCS		1/7			C	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0032794	PMID:27912044	PCS		3/7			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0001270	PMID:27912044	PCS		4/6			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0012444	PMID:27912044	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0000737	PMID:27912044	PCS		3/4			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0020221	PMID:27912044	PCS		1/7			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0020045	PMID:27912044	PCS		1/4			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0002119	PMID:27912044	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0000219	PMID:27912044	PCS		2/4			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0025116	PMID:27912044	PCS		4/7			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0001249	PMID:27912044	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0001942	PMID:27912044	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0003623	PMID:27912044	PCS		6/7			C	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0000750	PMID:27912044	PCS		5/6			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0001263	PMID:27912044	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0002151	PMID:27912044	PCS		4/6			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0005484	PMID:27912044	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0010851	PMID:27912044	PCS		5/7			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0002093	PMID:27912044	PCS	HP:0003623	3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0032792	PMID:27912044	PCS		4/4			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0000629	PMID:27912044	PCS		1/4			P	HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0000007	PMID:27912044	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0002104	PMID:27912044	PCS	HP:0003623	1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617290	Epilepsy, early-onset, vitamin b6-dependent		HP:0001336	PMID:27912044	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:613790	Complement component 8 deficiency, type I		HP:0001287	OMIM:613790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613790	Complement component 8 deficiency, type I		HP:0004434	OMIM:613790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613790	Complement component 8 deficiency, type I		HP:0000007	OMIM:613790	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613790	Complement component 8 deficiency, type I		HP:0002725	OMIM:613790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203760	Alpha-2-deficient collagen disease		HP:0001166	OMIM:203760	IEA					P	HPO:iea[2009-02-17]
OMIM:203760	Alpha-2-deficient collagen disease		HP:0001519	OMIM:203760	IEA					P	HPO:iea[2009-02-17]
OMIM:203760	Alpha-2-deficient collagen disease		HP:0001939	OMIM:203760	IEA					P	HPO:iea[2009-02-17]
OMIM:203760	Alpha-2-deficient collagen disease		HP:0000007	OMIM:203760	IEA					I	HPO:iea[2009-02-17]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000483	PMID:27839873	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0003676	OMIM:617284	TAS					C	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000486	PMID:27839873	PCS		1/6			P	HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001332	PMID:27839873	PCS		6/6		HP:0012837	P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0004322	PMID:27839873	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001270	PMID:27839873	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0012048	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0012049	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0100543	OMIM:617284	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0012179	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0011463	PMID:27839873	PCS		2/6			C	HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0003829	OMIM:617284	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000414	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000473	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000252	PMID:27839873	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0003621	PMID:27839873	PCS		4/6			C	HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000750	PMID:27839873	PCS		4/6			P	HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000496	OMIM:617284	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001288	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001260	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001263	PMID:27839873	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001618	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0030051	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001257	OMIM:617284	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0000006	PMID:27839873	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0002544	OMIM:617284	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001337	PMID:27839873	PCS		1/6			P	HPO:probinson[2022-08-23]
OMIM:617284	Dystonia 28, childhood-onset		HP:0001336	OMIM:617284	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000286	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000340	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000483	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000486	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000189	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0002188	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001250	PMID:37054711	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001272	PMID:37054711	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001252	PMID:37054711	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001274	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0003593	PMID:37054711	PCS		2/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001270	PMID:37054711	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000280	PMID:37054711	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0012444	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0011463	PMID:37054711	PCS		4/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000316	PMID:37054711	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0002119	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000219	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000278	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0009800	PMID:37054711	PCS		2/2			H	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000556	PMID:37054711	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001622	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0003623	PMID:37054711	PCS		8/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000154	PMID:37054711	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0002059	PMID:37054711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0006879	PMID:37054711	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000252	PMID:37054711	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001363	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000750	PMID:37054711	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001321	PMID:37054711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0002057	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0002352	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000193	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0002198	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000350	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0011344	PMID:37054711	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0030890	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000007	PMID:37054711	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000648	PMID:37054711	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0001511	PMID:37054711	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000545	PMID:37054711	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000325	PMID:37054711	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000369	PMID:37054711	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0009879	PMID:37054711	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620428	Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities		HP:0000445	PMID:37054711	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0002980	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000882	PMID:20887961	PCS		1/4			P	HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000160	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0003031	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0010493	OMIM:600920	TAS					P	HPO:probinson[2012-06-03]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000678	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001847	PMID:20887961	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0002857	PMID:29378527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0006236	OMIM:600920	IEA					P	HPO:iea[2012-06-03]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0006633	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001763	PMID:29378527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001249	PMID:20887961	PCS		0/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001601	OMIM:600920	IEA					P	HPO:skoehler[2010-06-18]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000358	PMID:20887961;PMID:29378527	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000175	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000452	OMIM:600920	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001382	PMID:29378527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001182	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0003083	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0012385	PMID:20887961;PMID:29378527	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0006380	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000327	PMID:20887961;OMIM:600920;PMID:29378527	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000767	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000007	PMID:20887961	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0002705	PMID:20887961	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000647	OMIM:600920	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000444	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0002987	OMIM:600920	IEA		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000960	PMID:20887961	PCS		1/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000883	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0034391	PMID:20887961;PMID:29378527	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000325	PMID:29378527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001215	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0030799	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000385	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0003577	PMID:20887961	PCS		4/4			C	HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0010946	PMID:20887961	PCS		1/4			P	HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0010307	OMIM:600920	IEA					P	HPO:skoehler[2010-06-18]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001195	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000581	PMID:20887961;OMIM:600920;PMID:29378527	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000460	PMID:29378527	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0005033	PMID:29378527	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0005709	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001822	PMID:29378527	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000218	PMID:20887961;PMID:29378527	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000895	PMID:29378527	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001786	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000411	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000894	PMID:20887961	PCS		1/4			P	HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000773	PMID:20887961	PCS		1/4			P	HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000534	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001166	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000396	PMID:20887961;PMID:29378527	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001363	OMIM:600920	TAS					P	HPO:skoehler[2014-08-24]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001762	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000232	PMID:20887961;PMID:29378527	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000430	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0003100	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0005001	PMID:29378527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000272	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:6000506	PMID:20887961;PMID:29378527	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0005280	PMID:29378527	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-05-19]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0009473	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0001836	OMIM:600920	IEA					P	HPO:iea[2009-02-17]
OMIM:600920	Van den Ende-Gupta syndrome		HP:0000347	PMID:20887961	PCS		4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0003763	OMIM:615493	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0000252	PMID:29302074	IEA		0/2			P	HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0002342	PMID:23390136;OMIM:615493	PCS		13/13			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0000750	PMID:23390136	PCS		3/3			P	HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0001250	PMID:23390136;PMID:29302074	PCS		3/5			P	HPO:probinson[2022-06-15];HPO:skoehler[2013-11-18];HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0001252	PMID:23390136	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0001263	PMID:23390136	PCS		3/3			P	HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0001290	OMIM:615493	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0000718	OMIM:615493	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0000007	PMID:23390136	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0000752	OMIM:615493	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0001257	PMID:23390136	PCS		3/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-06-15]
OMIM:615493	Intellectual developmental disorder, autosomal recessive 37		HP:0001249	PMID:29302074	PCS		2/2			P	HPO:probinson[2022-06-15]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0003621	OMIM:103900	TAS					C	HPO:probinson[2022-09-04]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0000079	OMIM:103900	IEA					P	HPO:iea[2009-02-17]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0000859	OMIM:103900	IEA					P	HPO:iea[2009-02-17]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0011463	OMIM:103900	TAS					C	HPO:probinson[2022-09-04]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0003581	OMIM:103900	TAS					C	HPO:probinson[2022-09-04]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0003351	OMIM:103900	IEA					P	HPO:iea[2009-02-17]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0008221	OMIM:103900	IEA					P	HPO:skoehler[2012-10-11]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0000822	OMIM:103900	IEA					P	HPO:iea[2009-02-17]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0000840	OMIM:103900	IEA					P	HPO:iea[2009-02-17]
OMIM:103900	Aldosteronism, glucocorticoid-remediable		HP:0000006	OMIM:103900	IEA					I	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0001276	PMID:23453665	PCS		2/5			P	HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0000343	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0001156	OMIM:218340	TAS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:218340	Temtamy syndrome		HP:0001250	PMID:23453665	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0001274	PMID:23453665	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0001252	OMIM:218340	TAS					P	HPO:skoehler[2014-11-26]
OMIM:218340	Temtamy syndrome		HP:0003593	PMID:23453665;OMIM:218340	PCS		14/15			C	HPO:skoehler[2013-05-03];HPO:probinson[2022-12-17];HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0000316	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000678	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000612	PMID:23453665	PCS		1/5			P	HPO:probinson[2012-06-05];HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0002119	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0001885	OMIM:218340	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218340	Temtamy syndrome		HP:0001763	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0003623	PMID:23453665	PCS		1/5			C	HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0002553	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000494	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0001762	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000276	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0001263	PMID:23453665	PCS		5/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0000394	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0012019	OMIM:218340	IEA					P	HPO:skoehler[2018-10-08]
OMIM:218340	Temtamy syndrome		HP:0001083	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0007074	PMID:23453665	PCS		1/5			P	HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0002827	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000007	PMID:23453665	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0000568	PMID:23453665	PCS		3/5			P	HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0001659	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000444	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0002007	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000685	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000567	PMID:23453665	PCS		3/5			P	HPO:probinson[2012-06-05];HPO:probinson[2022-12-17]
OMIM:218340	Temtamy syndrome		HP:0000369	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000347	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000545	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0004942	OMIM:218340	IEA					P	HPO:iea[2009-02-17]
OMIM:218340	Temtamy syndrome		HP:0000742	PMID:23453665	PCS		1/5			P	HPO:probinson[2022-12-17]
OMIM:620400	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9		HP:0001882	PMID:32139460	PCS		1/5			P	HPO:probinson[2024-03-01]
OMIM:620400	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9		HP:0001909	PMID:32139460	PCS		2/7			P	HPO:probinson[2024-03-01]
OMIM:620400	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9		HP:0003581	PMID:32139460	PCS		4/4			C	HPO:probinson[2024-03-01]
OMIM:620400	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9		HP:0002206	PMID:32139460	PCS		3/5			P	HPO:probinson[2024-03-01]
OMIM:620400	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9		HP:0031413	PMID:32139460	PCS		5/5			P	HPO:probinson[2024-03-01]
OMIM:620400	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9		HP:0000006	PMID:32139460	PCS					I	HPO:probinson[2024-03-01]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0003345	PMID:18795243	PCS		28/48			P	HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0011979	PMID:18795243	PCS		25/48			P	HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia IIA		HP:0003581	PMID:24331334	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:171400	Multiple endocrine neoplasia IIA		HP:0025388	PMID:24331334	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0002251	OMIM:171400	IEA					P	HPO:iea[2009-02-17]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0032346	OMIM:171400	TAS					P	HPO:skoehler[2019-04-18]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0011978	PMID:18795243	IEA		28/48			P	HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0011781	PMID:30085596	PCS					P	HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia IIA		HP:0011462	PMID:24331334	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:171400	Multiple endocrine neoplasia IIA		HP:0100735	PMID:24331334	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0003639	PMID:18795243	PCS		36/48			P	HPO:iea[2009-02-17];HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0000822	PMID:18795243	PCS		13/54			P	HPO:iea[2009-02-17];HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0000843	PMID:24331334;PMID:24152999	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:iea[2009-02-17];HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0100749	PMID:18795243	PCS		3/54			P	HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0003528	PMID:24331334	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0002315	PMID:18795243	PCS		5/54			P	HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0003118	OMIM:171400	IEA					P	HPO:iea[2009-02-17]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0002865	PMID:24331334;PMID:29465928;PMID:22274720	PCS		17/30			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:iea[2009-02-17];HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0001962	PMID:18795243	PCS		10/54			P	HP:probinson[2019-02-23]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0000006	PMID:24331334	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-06-29]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0002897	OMIM:171400	IEA					P	HPO:iea[2009-02-17]
OMIM:171400	Multiple endocrine neoplasia, type IIA		HP:0002666	PMID:24331334;PMID:22274720;PMID:18795243	PCS		67/189			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:iea[2009-02-17];HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0002850	PMID:30040974	PCS		1/2			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0002037	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0003621	PMID:30336224	PCS		1/1			C	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0005764	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0001894	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0002583	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0003593	PMID:30040974	PCS		1/2			C	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0011108	PMID:30040974	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0010976	PMID:30040974	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0011897	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0012177	PMID:30040974	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0012311	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0033351	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0011463	PMID:30040974	PCS		1/2			C	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0000007	PMID:30040974	PCS					I	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0006532	PMID:30040974	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0002720	PMID:30040974;PMID:30336224	PCS		3/3			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0004315	PMID:30040974;PMID:30336224	PCS		3/3			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0002028	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:619281	Immunodeficiency 14B, autosomal recessive		HP:0001974	PMID:30336224	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:175100	Adenomatous polyposis coli		HP:0001012	OMIM:175100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175100	Adenomatous polyposis coli		HP:0002884	PMID:1329510	PCS		2/470			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0030731	OMIM:175100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:175100	Adenomatous polyposis coli		HP:0004783	https://www.ncbi.nlm.nih.gov/books/NBK1345/	PCS		90%			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0200040	PMID:31062380	PCS		2/31			P	HPO:iea[2010-07-08];HPO:probinson[2021-02-26]
OMIM:175100	Adenomatous polyposis coli		HP:0100246	PMID:31062380	PCS		3/31			P	HPO:iea[2010-07-08];HPO:probinson[2021-02-26]
OMIM:175100	Adenomatous polyposis coli		HP:0011068	OMIM:175100	TAS					P	HPO:skoehler[2013-05-31]
OMIM:175100	Adenomatous polyposis coli		HP:0006771	PMID:14960520	PCS		5%			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0008256	PMID:11156460	PCS		13%			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0000953	OMIM:175100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175100	Adenomatous polyposis coli		HP:0005227	PMID:31062380	PCS		31/31			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:175100	Adenomatous polyposis coli		HP:0000670	OMIM:175100	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0007649	PMID:3821797	PCS		37/41			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:175100	Adenomatous polyposis coli		HP:0002895	PMID:22425061	PCS		6%			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0003003	PMID:31062380	PCS		7/31			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:175100	Adenomatous polyposis coli		HP:0010619	OMIM:175100	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0004394	OMIM:175100	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0011069	OMIM:175100	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0010614	OMIM:175100	PCS		HP:0040283			P	HPO:iea[2010-07-08]
OMIM:175100	Adenomatous polyposis coli		HP:0100245	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=fap	PCS		10%			P	HPO:iea[2010-07-08]
OMIM:175100	Adenomatous polyposis coli		HP:0009592	OMIM:175100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175100	Adenomatous polyposis coli		HP:0010562	OMIM:175100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175100	Adenomatous polyposis coli		HP:0000706	OMIM:175100	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0006744	OMIM:175100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175100	Adenomatous polyposis coli		HP:0000006	PMID:31062380	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:175100	Adenomatous polyposis coli		HP:0002885	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=fap	PCS		1%			P	HPO:iea[2009-02-17]
OMIM:175100	Adenomatous polyposis coli		HP:0006722	OMIM:175100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0008905	PMID:30478137	PCS	HP:0003593	2/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0001212	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000343	PMID:30478137	PCS		2/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0002188	PMID:30478137	PCS		1/2		HP:0012825	P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0012623	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000319	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0011220	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000954	PMID:30478137	PCS		1/2		HP:0012833	P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0002999	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000956	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000256	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0001601	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0001348	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0001187	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000494	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000431	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25];HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000470	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0002829	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0040024	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000007	PMID:30478137	PCS					I	HPO:probinson[2020-06-25];HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0009237	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0006467	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0001357	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0009778	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000520	PMID:30478137	PCS		1/2		HP:0012825	P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0000347	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0001513	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:618821	Rhizomelic limb shortening with dysmorphic features		HP:0001655	PMID:30478137	PCS		1/2			P	HPO:probinson[2020-06-25]
OMIM:138000	Glomuvenous malformations		HP:0001939	OMIM:138000	IEA					P	HPO:iea[2009-02-17]
OMIM:138000	Glomuvenous malformations		HP:0000006	OMIM:138000	IEA					I	HPO:iea[2009-02-17]
OMIM:138000	Glomuvenous malformations		HP:0000951	OMIM:138000	IEA					P	HPO:iea[2009-02-17]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003554	PMID:33744911	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0001771	PMID:39548192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003236	PMID:32165108;PMID:39548192;PMID:28501893	PCS		6/7			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003555	PMID:26718575;PMID:39548192;PMID:28501893	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003431	PMID:28501893	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0000365	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003596	PMID:33744911;PMID:31403083;PMID:26718575;PMID:28501893	PCS		10/15			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003551	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003394	PMID:26718575	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002380	PMID:26718575	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0033202	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0012548	PMID:33744911;PMID:31403083;PMID:26718575;PMID:32165108;PMID:28501893	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0033685	PMID:26718575	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0033201	PMID:31403083	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0100297	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0011462	PMID:33744911;PMID:31403083;PMID:32165108;PMID:28501893	PCS		6/15			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002938	PMID:31403083;PMID:32165108	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0009027	PMID:31403083;PMID:26718575;PMID:28501893	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003547	PMID:33744911	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003306	PMID:39548192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0020203	PMID:28501893	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003546	PMID:39548192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003202	PMID:33744911	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0000011	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003687	PMID:31403083;PMID:26718575;PMID:39548192;PMID:28501893	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003445	PMID:26718575	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0011808	PMID:31403083	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002792	PMID:33744911	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0010830	PMID:31403083;PMID:26718575;PMID:32165108	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0034392	PMID:32165108	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0009053	PMID:31403083;PMID:26718575;PMID:32165108;PMID:28501893	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002505	PMID:28501893	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:6000490	PMID:26718575	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003438	PMID:31403083	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0000006	PMID:26718575	PCS					I	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003557	PMID:33744911;PMID:31403083;PMID:39548192	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0025406	PMID:31403083;PMID:32165108	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002149	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0030237	PMID:31403083	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003376	PMID:31403083;PMID:26718575	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0008948	PMID:26718575	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003691	PMID:31403083;PMID:26718575;PMID:32165108;PMID:39548192	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0005991	PMID:32165108	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0100750	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0100595	PMID:31403083;PMID:32165108;PMID:28501893	PCS		5/7			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0000819	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0007340	PMID:39548192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0032341	PMID:33744911;PMID:31403083;PMID:32165108;PMID:39548192	PCS		3/7			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0008994	PMID:32165108;PMID:28501893	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003805	PMID:33744911;PMID:31403083;PMID:26718575;PMID:32165108;PMID:28501893	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002515	PMID:33744911	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002878	PMID:33744911	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0025238	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0001626	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0008997	PMID:39548192;PMID:28501893	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002910	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003325	PMID:33744911	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003722	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003621	PMID:39548192	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002650	PMID:39548192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0001288	PMID:33744911;PMID:31403083	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0001761	PMID:31403083;PMID:39548192	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0001284	PMID:32165108	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002093	PMID:33744911	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0010535	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0008180	PMID:26718575	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0008981	PMID:39548192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0033200	PMID:31403083	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0009830	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0000822	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0001638	PMID:31403083	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0002527	PMID:31403083	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0040129	PMID:33744911;PMID:32165108	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621078	Myopathy, myofibrillar, 13, with rimmed vacuoles		HP:0003458	PMID:26718575;PMID:39548192	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0002153	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0001085	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0005652	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0003155	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0003581	PMID:34668226	PCS		1/1			C	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0012625	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0011002	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0011001	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0001903	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0002737	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0000007	PMID:34668226	PCS					I	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0000843	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0007663	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0008897	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0002756	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620366	Osteopetrosis, autosomal recessive 9		HP:0003259	PMID:34668226	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0003236	PMID:30283131	PCS	HP:0003593	5/9			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001410	PMID:30283131	PCS	HP:0003593	5/9			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0000365	PMID:30283131	PCS	HP:0003593	1/1			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0011924	PMID:30283131	PCS		4/7			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001790	PMID:30283131	PCS	HP:0030674	3/9			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0011923	PMID:30283131	PCS		6/7			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0008163	PMID:30283131	PCS	HP:0003593	1/2			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001639	PMID:30283131	PCS	HP:0003593	9/9			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001903	PMID:30283131	PCS	HP:0003593	7/7			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0000007	PMID:30283131	PCS					I	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001943	PMID:30283131	PCS	HP:0003593	2/9			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0008347	PMID:30283131	PCS		6/7			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001511	PMID:30283131	PCS	HP:0030674	2/9			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001522	PMID:30283131	PCS		6/9			C	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0003811	PMID:30283131	PCS		3/9			C	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0001622	PMID:30283131	PCS	HP:0003577	2/9			P	HPO:probinson[2020-07-06]
OMIM:618835	Combined oxidative phosphorylation deficiency 40		HP:0003128	PMID:30283131	PCS	HP:0003593	9/9			P	HPO:probinson[2020-07-06]
OMIM:620372	Hypersulfaturia		HP:0006649	PMID:36719378	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620372	Hypersulfaturia		HP:0011462	PMID:36719378	PCS		1/1			C	HPO:probinson[2023-06-14]
OMIM:620372	Hypersulfaturia		HP:0012613	PMID:36719378	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620372	Hypersulfaturia		HP:6000854	PMID:36719378	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:620372	Hypersulfaturia		HP:0000007	PMID:36719378	PCS					I	HPO:probinson[2023-06-14]
OMIM:620372	Hypersulfaturia		HP:0000787	PMID:36719378	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0003774	PMID:25782674	PCS		2/11			P	HPO:probinson[2017-06-17]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0003676	OMIM:616818	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0012574	PMID:25782674	PCS					P	HPO:probinson[2017-06-17]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0000794	PMID:25782674	PCS					P	HPO:probinson[2017-06-17]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0000790	PMID:25782674	PCS		5/8			P	HPO:probinson[2017-06-17]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0011462	PMID:25782674	PCS					C	HPO:probinson[2017-06-17]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0000822	PMID:25782674	PCS		3/10			P	HPO:probinson[2017-06-17]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0000093	PMID:25782674	PCS		1/8			P	HPO:probinson[2017-06-17]
OMIM:616818	Iga nephropathy, susceptibility to, 3		HP:0000006	PMID:25782674	PCS					I	HPO:probinson[2017-06-17]
OMIM:246200	Donohue syndrome		HP:0001176	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000040	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0003074	OMIM:246200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:246200	Donohue syndrome		HP:0000280	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0003270	PMID:24498630	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0012471	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0000998	PMID:24498630	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000956	PMID:24498630	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0008897	PMID:24498630	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:246200	Donohue syndrome		HP:0001007	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0003623	PMID:24498630	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0003202	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0002750	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0002035	PMID:24498630	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0003162	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0030948	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0002908	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0000007	OMIM:246200	IEA					I	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000403	PMID:24498630	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0000400	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0008887	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0004405	PMID:24498630	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000520	PMID:24498630	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000842	PMID:24498630	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000369	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000962	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0001034	OMIM:246200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:246200	Donohue syndrome		HP:0001396	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0003577	PMID:24498630	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0000065	PMID:24498630	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0030796	PMID:24498630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0012408	PMID:24498630	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0002164	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0001395	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0002240	PMID:24498630	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0011998	OMIM:246200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:246200	Donohue syndrome		HP:0001508	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0002719	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0001988	PMID:24498630	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0000212	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000179	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000138	PMID:24498630	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0001744	PMID:24498630	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0000154	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0001561	PMID:24498630	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0000274	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0004510	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000826	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0001639	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0001712	PMID:24498630	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:246200	Donohue syndrome		HP:0001833	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0008665	PMID:24498630	PCS		1/1			P	HPO:skoehler[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0004428	OMIM:246200	IEA					P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0001511	PMID:24498630	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:246200	Donohue syndrome		HP:0000105	PMID:24498630	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-21]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0002014	PMID:19692703	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0003565	PMID:19692703	PCS		1/1			P	HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0002719	OMIM:613960	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0002583	PMID:19692703	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0011463	PMID:19692703	PCS		1/1			C	HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0011127	PMID:19692703	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0000007	PMID:19692703	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0011108	OMIM:613960	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0011107	PMID:19692703	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0002027	PMID:19692703	PCS		1/1			P	HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0005218	PMID:19692703	PCS		1/1			P	HPO:probinson[2023-03-02]
OMIM:613960	Chronic granulomatous disease 3, autosomal recessive		HP:0011227	PMID:19692703	PCS		1/1			P	HPO:probinson[2023-03-02]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000286	PMID:28092684	PCS		1/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001250	PMID:28092684	PCS					P	HPO:skoehler[2012-12-30];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001010	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001252	PMID:28092684	PCS		8/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001251	PMID:28092684	PCS		2/5			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0012110	PMID:28092684	PCS		12/12			P	HPO:skoehler[2014-04-22];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000639	PMID:28092684	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000954	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000238	PMID:28092684	PCS		1/12			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001324	PMID:28092684	PCS		3/3			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001007	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001249	PMID:28092684	PCS		9/9			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000253	PMID:28092684	PCS		12/13			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0003202	PMID:28092684	PCS		3/3			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000054	PMID:28092684	PCS		4/8			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001344	OMIM:614969	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001266	PMID:28092684	PCS		2/6			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002079	PMID:28092684	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0011968	PMID:28092684	PCS		6/6			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001263	PMID:28092684	PCS		13/13			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000729	PMID:28092684	PCS		1/3			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000007	PMID:28092684	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000648	PMID:28092684	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000768	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000400	PMID:28092684	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001258	PMID:28092684	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001257	PMID:28092684	PCS		7/10			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002104	PMID:28092684	PCS		3/13			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000369	PMID:28092684	PCS		1/11			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001336	PMID:28092684	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001276	PMID:28092684	PCS		8/10			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002003	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0003577	PMID:28092684	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002002	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002365	PMID:28092684	PCS		10/10			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000062	PMID:28092684	PCS		10/12			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000657	PMID:28092684	PCS		2/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001308	PMID:28092684	PCS		1/5			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002119	PMID:28092684	PCS		6/12			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000218	PMID:28092684	PCS		3/12			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000455	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000336	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000215	PMID:28092684	PCS		2/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001347	PMID:28092684	PCS		5/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002179	PMID:28092684	PCS		1/5			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0002059	PMID:28092684	PCS					P	HPO:skoehler[2012-12-30];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000431	PMID:28092684	PCS		2/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0001321	PMID:28092684	PCS					P	HPO:skoehler[2014-04-22];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000664	PMID:28092684	PCS		1/13			P	HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000347	PMID:28092684	PCS		2/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614969	Pontocerebellar hypoplasia, type 7		HP:0000028	PMID:28092684	PCS		4/5			P	HPO:probinson[2022-09-25]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0002982	OMIM:210720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000882	OMIM:210720	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0001377	OMIM:210720	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0003275	OMIM:210720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0003031	OMIM:210720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000957	OMIM:210720	TAS					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0002812	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0008897	OMIM:210720	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0007402	OMIM:210720	TAS					P	HPO:skoehler[2015-12-30]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000278	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0001249	OMIM:210720	TAS					P	HPO:probinson[2010-06-18]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000252	OMIM:210720	TAS					P	HPO:probinson[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000890	OMIM:210720	TAS		HP:0040283			P	HPO:probinson[2012-05-27]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0002750	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0001263	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000691	OMIM:210720	TAS		HP:0040283			P	HPO:probinson[2012-05-06]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0100263	OMIM:210720	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0006461	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0005819	OMIM:210720	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000448	OMIM:210720	TAS					P	HPO:skoehler[2012-10-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000007	OMIM:210720	TAS					I	HPO:probinson[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0004209	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0006587	OMIM:210720	TAS		HP:0040283			P	HPO:probinson[2012-05-27]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0002986	OMIM:210720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000047	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0002866	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0005978	OMIM:210720	TAS					P	HPO:probinson[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0003015	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000340	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000582	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000540	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0003498	OMIM:210720	TAS					P	HPO:probinson[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0001156	OMIM:210720	TAS					P	HPO:skoehler[2014-11-26]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0011834	OMIM:210720	TAS					P	HPO:probinson[2012-05-06]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0010034	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0006297	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0008551	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0009882	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000774	OMIM:210720	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0001620	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0003100	PMID:15372530	PCS					P	HPO:probinson[2015-03-21]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0002690	OMIM:210720	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0009193	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0010579	OMIM:210720	TAS		HP:0040283			P	HPO:probinson[2012-06-10]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000826	OMIM:210720	TAS					P	HPO:probinson[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0010583	OMIM:210720	TAS		HP:0040283			P	HPO:probinson[2012-06-10]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0000426	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0002209	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0001956	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0001511	OMIM:210720	IEA					P	HPO:iea[2009-02-17]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0004944	OMIM:210720	TAS					P	HPO:probinson[2012-05-06]
OMIM:210720	Microcephalic osteodysplastic primordial dwarfism, type II		HP:0006645	OMIM:210720	TAS		HP:0040283			P	HPO:probinson[2012-05-27]
OMIM:242700	Immune defect due to absence of thymus		HP:0005359	OMIM:242700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:242700	Immune defect due to absence of thymus		HP:0005403	PMID:31566583	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:242700	Immune defect due to absence of thymus		HP:0002972	OMIM:242700	IEA					P	HPO:iea[2009-02-17]
OMIM:242700	Immune defect due to absence of thymus		HP:0006538	OMIM:242700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:242700	Immune defect due to absence of thymus		HP:0002110	OMIM:242700	IEA					P	HPO:iea[2009-02-17]
OMIM:242700	Immune defect due to absence of thymus		HP:0002097	OMIM:242700	IEA					P	HPO:iea[2009-02-17]
OMIM:242700	Immune defect due to absence of thymus		HP:0031545	PMID:31566583	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:242700	Immune defect due to absence of thymus		HP:0001508	PMID:31566583	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:242700	Immune defect due to absence of thymus		HP:0001888	OMIM:242700	IEA					P	HPO:iea[2009-02-17]
OMIM:242700	Immune defect due to absence of thymus		HP:0000964	OMIM:242700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:242700	Immune defect due to absence of thymus		HP:0000007	PMID:31566583	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:242700	Immune defect due to absence of thymus		HP:0004429	PMID:31566583	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:242700	Immune defect due to absence of thymus		HP:0006532	OMIM:242700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:242700	Immune defect due to absence of thymus		HP:0000999	OMIM:242700	IEA					P	HPO:iea[2009-02-17]
OMIM:242700	Immune defect due to absence of thymus		HP:0001433	OMIM:242700	IEA					P	HPO:iea[2009-02-17]
OMIM:242700	Immune defect due to absence of thymus		HP:0003623	PMID:31566583	PCS		1/1			C	HPO:probinson[2022-09-04]
OMIM:242700	Immune defect due to absence of thymus		HP:0002028	OMIM:242700	IEA					P	HPO:iea[2009-02-17]
OMIM:617253	Seckel syndrome 10		HP:0001397	PMID:25105364	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0003510	PMID:25105364	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0003016	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0000541	PMID:25105364	PCS	HP:0003577	1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0005112	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0010609	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0003076	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0031964	OMIM:617253	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617253	Seckel syndrome 10		HP:0000819	OMIM:617253	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617253	Seckel syndrome 10		HP:0012371	PMID:25105364	PCS		2/2			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0008232	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0000855	PMID:25105364	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0000956	PMID:25105364	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0040217	OMIM:617253	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617253	Seckel syndrome 10		HP:0031956	OMIM:617253	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617253	Seckel syndrome 10		HP:0000252	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0002155	PMID:25105364	PCS	HP:0011463	2/2			P	HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0011969	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0003100	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0040270	OMIM:617253	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617253	Seckel syndrome 10		HP:0010579	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0000308	PMID:25105364	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0001735	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0000822	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0000007	PMID:25105364	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-04]
OMIM:617253	Seckel syndrome 10		HP:0001635	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0001714	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617253	Seckel syndrome 10		HP:0001952	OMIM:617253	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0000252	PMID:24480542	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0010627	PMID:24480542	PCS		3/3			P	HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0002750	PMID:24480542	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0004322	PMID:24480542	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0003593	PMID:24480542	PCS		3/3			C	HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0000007	PMID:24480542	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0000824	PMID:24480542	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0008897	PMID:24480542	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0001956	OMIM:618160	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0002007	PMID:24480542	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-21]
OMIM:618160	Pituitary hormone deficiency, combined or isolated, 7		HP:0012743	OMIM:618160	IEA					P	HPO:skoehler[2019-04-18]
OMIM:180360	RHINY		HP:0000233	OMIM:180360	TAS					P	HPO:probinson[2013-12-17]
OMIM:180360	RHINY		HP:0000023	OMIM:180360	IEA					P	HPO:iea[2009-02-17]
OMIM:180360	RHINY		HP:0000463	OMIM:180360	IEA					P	HPO:iea[2009-02-17]
OMIM:180360	RHINY		HP:0003196	OMIM:180360	TAS					P	HPO:skoehler[2009-02-17]
OMIM:180360	RHINY		HP:0000006	OMIM:180360	IEA					I	HPO:iea[2009-02-17]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0003621	PMID:23891471	PCS		1/5			C	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0001696	PMID:23891469	PCS	HP:0003577	8/13			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0001696	PMID:23891471	PCS		3/10			P	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0001651	PMID:23891471	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0002110	PMID:23891469;PMID:23891471	PCS		20/31			P	HPO:probinson[2022-03-05];HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0003593	PMID:23891471	PCS		2/5			C	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0033036	PMID:23891469;PMID:23891471	PCS		12/12			P	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0012207	PMID:23891471	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0100582	PMID:23891471	PCS		1/10			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0011108	PMID:23891469	PCS		22/35			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0012259	PMID:23891469;PMID:23891471	PCS		20/21			P	HPO:probinson[2022-03-05];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0200073	PMID:23891471	PCS					P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0012265	PMID:23891471	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0011463	PMID:23891471	PCS		2/5			C	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0012384	PMID:23891471	PCS		4/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0012263	PMID:23891469	PCS		7/7			P	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0000789	PMID:23891469	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0000403	PMID:23891469	PCS		28/36			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0000007	PMID:23891469	PCS					I	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0002205	PMID:23891471	PCS		2/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0002643	PMID:23891469;PMID:23891471	PCS		34/41			P	HPO:probinson[2022-03-05]
OMIM:615444	Ciliary dyskinesia, primary, 22		HP:0004469	PMID:23891471	PCS					P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-05]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000286	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0001572	PMID:31207318	PCS					P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002202	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002540	PMID:31207318	PCS		2/2			P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000486	PMID:30624672;PMID:31207318	PCS		3/3			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0001410	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000463	PMID:30624672;PMID:31207318	PCS		3/3			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002066	PMID:31207318	PCS					P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002162	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002580	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0001290	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002280	PMID:31207318	PCS		1/2			P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0012110	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0001508	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0100704	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000316	PMID:31207318	PCS					P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000954	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0001305	PMID:31207318	PCS		1/2			P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000219	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000218	PMID:30624672;PMID:31207318	PCS		11/11			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0025336	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002019	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000215	PMID:31207318	PCS					P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0025517	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000396	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0001320	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000252	PMID:30624672;PMID:31207318	PCS		11/11			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0006956	PMID:31207318	PCS					P	HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002133	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002079	PMID:30624672;PMID:31207318	PCS		3/3			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0011968	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002099	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0011344	PMID:30624672;PMID:31207318	PCS		3/3			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0010535	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000969	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000007	PMID:31207318	PCS					I	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0001217	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000527	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0002205	PMID:30624672	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618606	Pontocerebellar hypoplasia, type 13		HP:0000322	PMID:31207318	PCS		1/2			P	HPO:probinson[2020-07-15]
OMIM:608415	Prolonged electroretinal response suppression 1		HP:0030512	PMID:14702087;PMID:19818506	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:608415	Prolonged electroretinal response suppression 1		HP:0030511	PMID:14702087;PMID:19818506	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:608415	Prolonged electroretinal response suppression 1		HP:0011463	PMID:14702087;PMID:19818506	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:608415	Prolonged electroretinal response suppression 1		HP:0000613	PMID:14702087;PMID:19818506	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:608415	Prolonged electroretinal response suppression 1		HP:0007663	PMID:14702087;PMID:19818506	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:608415	Prolonged electroretinal response suppression 1		HP:0000007	PMID:14702087	PCS					I	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:606438	Huntington disease-like 2		HP:0030216	PMID:11914418	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:606438	Huntington disease-like 2		HP:0002345	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0002067	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0003596	PMID:11914418;PMID:11694876	PCS		4/4			C	HPO:probinson[2023-03-31]
OMIM:606438	Huntington disease-like 2		HP:0001332	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0002354	PMID:11914418	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:606438	Huntington disease-like 2		HP:0002120	PMID:11914418	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:606438	Huntington disease-like 2		HP:0001260	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0002063	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0002072	PMID:11914418	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0000716	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0000738	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0000726	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0000737	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0000739	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0007123	PMID:11914418	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:606438	Huntington disease-like 2		HP:0000746	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0001824	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0000741	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:606438	Huntington disease-like 2		HP:0000006	PMID:11694876	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606438	Huntington disease-like 2		HP:0001347	OMIM:606438	IEA					P	HPO:iea[2009-02-17]
OMIM:273250	46, XY sex reversal 11		HP:0012870	OMIM:273250	TAS					P	HPO:skoehler[2015-01-21]
OMIM:273250	46, XY sex reversal 11		HP:0008197	PMID:31337883	PCS					P	HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0011969	PMID:31337883	PCS					P	HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0100779	PMID:31337883	PCS		1/9	FEMALE		P	HPO:probinson[2020-07-26];HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0000151	PMID:31337883	PCS			FEMALE		P	HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0008232	PMID:31337883	PCS					P	HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0040171	PMID:31337883	PCS					P	HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0000812	OMIM:273250	IEA					P	HPO:skoehler[2009-02-17]
OMIM:273250	46, XY sex reversal 11		HP:0031103	PMID:31337883	PCS					P	HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0008723	PMID:31337883	IEA		7/9	FEMALE		P	HPO:probinson[2020-07-26];HPO:probinson[2020-07-26]
OMIM:273250	46, XY sex reversal 11		HP:0000006	PMID:31337883	PCS					I	HPO:probinson[2020-07-19]
OMIM:273250	46, XY sex reversal 11		HP:0000786	PMID:31337883	PCS		2/9	FEMALE		P	HPO:probinson[2020-07-26]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0003323	PMID:32403198	PCS		11/11			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0003236	PMID:32403198	PCS		9/9			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0008209	PMID:32403198	PCS		3/3	FEMALE		P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0003577	PMID:32403198	PCS		11/11			C	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0003687	PMID:32403198	PCS		9/9			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0002650	PMID:32403198	PCS		4/10			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0004322	PMID:32403198	PCS		8/11			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0002033	PMID:32403198	PCS					P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0033686	PMID:32403198	PCS		1/9			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0001270	PMID:32403198	PCS		1/1			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0002093	PMID:32403198	PCS		8/10			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0001508	PMID:32403198	PCS		7/10			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0000407	PMID:32403198	PCS	HP:0003577	10/11			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0032341	PMID:32403198	PCS		2/4			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0008222	PMID:32403198	PCS		3/3			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0000007	PMID:32403198	PCS					I	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0001558	PMID:32403198	PCS	HP:0011461				P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0003805	PMID:32403198	PCS		9/9			P	HPO:probinson[2021-10-30]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0002505	PMID:32403198	PCS	HP:0003621	5/11			P	HPO:probinson[2022-04-15]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0025717	PMID:32403198	PCS		2/9			P	HPO:probinson[2022-02-03]
OMIM:619518	Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome		HP:0001612	PMID:32403198	PCS					P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0001331	OMIM:601357	TAS					P	HPO:skoehler[2013-04-18]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0009827	OMIM:601357	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0003577	OMIM:601357	TAS					C	HPO:skoehler[2012-10-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0002650	OMIM:601357	IEA					P	HPO:iea[2009-02-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0001360	OMIM:601357	IEA					P	HPO:iea[2009-02-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0003097	OMIM:601357	IEA					P	HPO:skoehler[2010-06-18]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0100336	OMIM:601357	TAS					P	HPO:probinson[2023-03-13]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0100337	OMIM:601357	TAS					P	HPO:probinson[2023-03-13]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0001849	OMIM:601357	IEA		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0001629	OMIM:601357	IEA					P	HPO:iea[2009-02-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0007035	OMIM:601357	IEA					P	HPO:iea[2009-02-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0001539	OMIM:601357	IEA					P	HPO:iea[2009-02-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0003745	OMIM:601357	TAS					I	HPO:skoehler[2015-12-30]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0000204	OMIM:601357	IEA					P	HPO:iea[2012-04-29]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0000589	OMIM:601357	IEA		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0000369	OMIM:601357	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601357	Brachial amelia, cleft lip, and holoprosencephaly		HP:0002006	OMIM:601357	IEA					P	HPO:skoehler[2010-06-20]
OMIM:618612	Lower urinary tract obstruction, congenital		HP:0000076	PMID:31051115	PCS		5/10			P	HPO:probinson[2020-07-10]
OMIM:618612	Lower urinary tract obstruction, congenital		HP:0010957	PMID:31051115	PCS		3/10			P	HPO:probinson[2020-07-10]
OMIM:618612	Lower urinary tract obstruction, congenital		HP:0000020	PMID:31051115	PCS		2/10			P	HPO:probinson[2020-07-10]
OMIM:618612	Lower urinary tract obstruction, congenital		HP:0008661	PMID:31051115	PCS		4/10			P	HPO:probinson[2020-07-10]
OMIM:618612	Lower urinary tract obstruction, congenital		HP:0100515	PMID:31051115	PCS		2/10			P	HPO:probinson[2020-07-10]
OMIM:618612	Lower urinary tract obstruction, congenital		HP:0000006	PMID:31051115	PCS					I	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:621093	Oocyte/zygote/embryo maturation arrest 22		HP:0034914	PMID:37052235;PMID:38177974	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621093	Oocyte/zygote/embryo maturation arrest 22		HP:0031516	PMID:37052235;PMID:37723834	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621093	Oocyte/zygote/embryo maturation arrest 22		HP:0025708	PMID:38177974	PCS		2/3			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621093	Oocyte/zygote/embryo maturation arrest 22		HP:0008222	PMID:37052235;PMID:37723834;PMID:38177974	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621093	Oocyte/zygote/embryo maturation arrest 22		HP:0011462	PMID:37052235;PMID:37723834;PMID:38177974	PCS		8/10			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621093	Oocyte/zygote/embryo maturation arrest 22		HP:0000007	PMID:37052235	PCS					I	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621093	Oocyte/zygote/embryo maturation arrest 22		HP:0033712	PMID:37052235;PMID:37723834;PMID:38177974	PCS		8/8			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:603554	Omenn syndrome		HP:0002014	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0001880	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0001596	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0003075	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0002240	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0001072	OMIM:603554	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603554	Omenn syndrome		HP:0002090	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0010976	OMIM:603554	TAS		20/20		HP:0012828	P	HPO:probinson[2009-02-17];HPO:skoehler[2012-10-17]
OMIM:603554	Omenn syndrome		HP:0001508	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0001903	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0002718	OMIM:603554	TAS					P	HPO:probinson[2012-06-08]
OMIM:603554	Omenn syndrome		HP:0000778	OMIM:603554	TAS					P	HPO:probinson[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0000007	OMIM:603554	IEA					I	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0001019	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0002716	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0004429	OMIM:603554	TAS					P	HPO:probinson[2012-06-08]
OMIM:603554	Omenn syndrome		HP:0001873	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0001744	OMIM:603554	IEA					P	HPO:iea[2009-02-17]
OMIM:603554	Omenn syndrome		HP:0002841	OMIM:603554	TAS					P	HPO:probinson[2012-06-08]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0002344	OMIM:261640	IEA					P	HPO:skoehler[2010-06-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001276	OMIM:261640	IEA					P	HPO:skoehler[2018-10-08]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0002067	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001332	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001250	OMIM:261640	IEA					P	HPO:iea[2009-02-17]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0002063	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0003593	OMIM:261640	TAS					C	HPO:skoehler[2015-12-30]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001251	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0000737	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0003623	PMID:8178819	PCS		2/2			C	HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001347	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0003785	PMID:8178819	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0008936	OMIM:261640	TAS					P	HPO:probinson[2009-02-17]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0000252	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0002015	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001300	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001266	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0011968	PMID:8178819	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0003781	OMIM:261640	TAS					P	HPO:skoehler[2015-01-04]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0002033	OMIM:261640	IEA					P	HPO:skoehler[2010-06-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0025455	PMID:8178819	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001263	PMID:8178819;OMIM:261640	PCS		11/12			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-20];HPO:skoehler[2019-02-22]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001262	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001518	PMID:8178819	PCS		1/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0002509	PMID:8178819	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001954	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0000007	PMID:8178819	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0004923	PMID:8178819	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-20]
OMIM:261640	Hyperphenylalaninemia, BH4-deficient, A		HP:0001337	OMIM:261640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:614028	Hyperalphalipoproteinemia 2		HP:0003563	PMID:19074352	IEA					P	HPO:probinson[2013-02-25]
OMIM:614028	Hyperalphalipoproteinemia 2		HP:0012184	PMID:19074352	IEA					P	HPO:probinson[2013-01-09]
OMIM:614028	Hyperalphalipoproteinemia 2		HP:0012153	PMID:19074352	IEA					P	HPO:probinson[2013-02-25]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:0100501	PMID:19462466	PCS		1/1			P	HPO:probinson[2024-03-14]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:0003621	PMID:19462466	PCS		1/1			C	HPO:probinson[2024-03-14]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:0002110	OMIM:613021	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:6000100	PMID:19462466	PCS		0/1			P	HPO:probinson[2024-03-14]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:0012092	PMID:19462466	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-14]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:0012236	PMID:19462466	PCS		1/1			P	HPO:skoehler[2013-04-02];HPO:probinson[2024-03-14]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:0000006	PMID:19462466	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:613021	Bronchiectasis with or without elevated sweat chloride 2		HP:0004469	OMIM:613021	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608367	Myopia 17		HP:0011530	OMIM:608367	PCS					P	HPO:probinson[2012-04-06]
OMIM:608367	Myopia 17		HP:0007819	OMIM:608367	PCS					P	HPO:probinson[2012-04-06]
OMIM:608367	Myopia 17		HP:0011003	OMIM:608367	PCS					P	HPO:probinson[2012-04-06]
OMIM:608367	Myopia 17		HP:0000006	OMIM:608367	PCS					I	HPO:probinson[2012-04-06]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0000252	PMID:22232082	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0003577	PMID:22232082	PCS		1/1			C	HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0000086	PMID:22232082	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0011835	PMID:22232082	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0010035	PMID:22232082	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0012799	PMID:22232082	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0040012	PMID:22232082	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0000007	PMID:22232082	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0009777	PMID:22232082	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0001643	PMID:22232082	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0001510	PMID:22232082	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0002984	PMID:22232082	PCS		1/1		HP:0012833	P	HPO:probinson[2022-03-15]
OMIM:617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0003974	PMID:22232082	PCS		1/1		HP:0012833	P	HPO:probinson[2022-03-15]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001276	PMID:30013181	PCS		1/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002521	PMID:30013181	PCS		1/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002540	PMID:30013181	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002089	PMID:30013181	PCS		0/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002365	PMID:30013181	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0004322	PMID:30013181	PCS		0/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001250	PMID:30013181	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001252	PMID:30013181	PCS		6/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001251	PMID:30013181	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0003593	PMID:30013181	PCS		7/7			C	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0032794	PMID:30013181	PCS		3/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0010862	PMID:30013181	PCS		7/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0012469	PMID:30013181	PCS		1/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0000238	PMID:30013181	PCS		0/5			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001302	PMID:30013181	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0000256	PMID:30013181	PCS		0/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001347	PMID:30013181	PCS		6/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002510	PMID:30013181	PCS		4/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001344	PMID:30013181	PCS		4/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002353	PMID:30013181	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001321	PMID:30013181	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002079	PMID:30013181	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0010819	PMID:30013181	PCS		6/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0005484	PMID:30013181	PCS		4/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0002194	PMID:30013181	PCS		7/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0011344	PMID:30013181	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0012434	PMID:30013181	PCS		7/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0034295	PMID:30013181	PCS		6/6			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0000729	PMID:30013181	PCS		7/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0000007	PMID:30013181	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0000648	PMID:30013181	PCS		0/7			P	HPO:probinson[2023-05-07]
OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9		HP:0001776	PMID:30013181	PCS		1/7			P	HPO:probinson[2023-05-07]
OMIM:188700	Tibia vara		HP:0010591	OMIM:188700	TAS					P	HPO:probinson[2013-04-01]
OMIM:188700	Tibia vara		HP:0002970	OMIM:188700	TAS					P	HPO:probinson[2013-04-01]
OMIM:188700	Tibia vara		HP:0000006	OMIM:188700	TAS					I	HPO:probinson[2009-02-17]
OMIM:188700	Tibia vara		HP:0010886	OMIM:188700	TAS					P	HPO:probinson[2013-04-01]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0001562	OMIM:274265	IEA					P	HPO:iea[2009-02-17]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0000818	OMIM:274265	IEA					P	HPO:iea[2009-02-17]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0002023	OMIM:274265	IEA					P	HPO:iea[2009-02-17]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0012300	OMIM:274265	TAS					P	HPO:probinson[2013-04-13]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0001939	OMIM:274265	IEA					P	HPO:iea[2009-02-17]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0002086	OMIM:274265	IEA					P	HPO:iea[2009-02-17]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0008631	OMIM:274265	TAS					P	HPO:probinson[2013-04-13]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0000007	OMIM:274265	IEA					I	HPO:iea[2009-02-17]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0001511	OMIM:274265	IEA					P	HPO:iea[2009-02-17]
OMIM:274265	Thymic-Renal-Anal-Lung dysplasia		HP:0000104	OMIM:274265	TAS					P	HPO:probinson[2013-04-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0003577	OMIM:616171	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000340	OMIM:616171	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0004322	PMID:25344692	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001272	OMIM:616171	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001250	PMID:25344692	PCS		1/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000482	PMID:25344692	PCS		2/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0012110	PMID:25344692	PCS		2/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000518	PMID:25344692	PCS		2/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0007165	PMID:25344692	PCS		1/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0100702	PMID:25344692	PCS		2/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0007401	OMIM:616171	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001249	PMID:25344692	PCS		7/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0002059	OMIM:616171	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000252	PMID:25344692	PCS		7/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001344	PMID:25344692	PCS		4/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001762	PMID:25344692	PCS		1/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001321	PMID:25344692	PCS		2/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001263	OMIM:616171	TAS				HP:0012829	P	HPO:skoehler[2015-02-22]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000448	OMIM:616171	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000007	PMID:25344692	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000568	OMIM:616171	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001338	PMID:25344692	PCS		2/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000648	OMIM:616171	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000505	OMIM:616171	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0001511	PMID:25344692	PCS		1/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0004626	PMID:25344692	PCS		1/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000543	OMIM:616171	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000488	OMIM:616171	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000520	OMIM:616171	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0002943	PMID:25344692	PCS		1/7			P	HPO:probinson[2023-03-13]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0000347	PMID:25344692	PCS		2/7			P	HPO:skoehler[2015-04-05]
OMIM:616171	Microcephaly and chorioretinopathy, autosomal recessive, 2		HP:0009879	OMIM:616171	TAS					P	HPO:skoehler[2015-02-22]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0002301	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0002367	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0003621	PMID:34320921	PCS		8/12			C	HPO:probinson[2022-12-11]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001289	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0002442	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001272	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0002076	PMID:34320921	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-11]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001250	OMIM:141500	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0002077	OMIM:141500	TAS					P	HPO:skoehler[2013-01-22]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001251	OMIM:141500	PCS					P	HPO:probinson[2012-04-06]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0002381	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0000709	OMIM:141500	TAS					P	HPO:skoehler[2013-01-22]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0000639	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0011462	PMID:34320921	PCS		4/12			C	HPO:probinson[2022-12-11]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0000739	OMIM:141500	TAS					P	HPO:skoehler[2013-01-22]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0008765	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0000713	OMIM:141500	TAS					P	HPO:skoehler[2013-01-22]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0002329	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001945	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001269	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001125	OMIM:141500	PCS					P	HPO:probinson[2012-04-06]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0000006	PMID:8898206	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-11]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001337	OMIM:141500	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:141500	Migraine, familial hemiplegic, 1		HP:0001259	OMIM:141500	IEA					P	HPO:iea[2009-02-17]
OMIM:616617	Heimler syndrome 2		HP:0000705	PMID:26387595	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:616617	Heimler syndrome 2		HP:0000407	PMID:26387595	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:616617	Heimler syndrome 2		HP:0001263	PMID:26387595	PCS		0/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-11]
OMIM:616617	Heimler syndrome 2		HP:0000678	PMID:26387595	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-11]
OMIM:616617	Heimler syndrome 2		HP:0000007	PMID:26387595	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:616617	Heimler syndrome 2		HP:0041093	PMID:26387595	PCS		4/4			P	HPO:probinson[2022-09-11]
OMIM:616617	Heimler syndrome 2		HP:0001763	OMIM:616617	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616617	Heimler syndrome 2		HP:0001820	PMID:26387595	PCS		2/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-11]
OMIM:145000	Hyperparathyroidism 1		HP:0008200	OMIM:145000	IEA					P	HPO:iea[2009-02-17]
OMIM:145000	Hyperparathyroidism 1		HP:0003072	OMIM:145000	IEA					P	HPO:iea[2009-02-17]
OMIM:145000	Hyperparathyroidism 1		HP:0000006	OMIM:145000	IEA					I	HPO:iea[2009-02-17]
OMIM:236730	Urofacial syndrome		HP:0010481	OMIM:236730	TAS					P	HPO:skoehler[2010-06-20]
OMIM:236730	Urofacial syndrome		HP:0000010	OMIM:236730	IEA					P	HPO:iea[2009-02-17]
OMIM:236730	Urofacial syndrome		HP:0005346	OMIM:236730	TAS					P	HPO:skoehler[2013-02-27]
OMIM:236730	Urofacial syndrome		HP:0000072	OMIM:236730	IEA					P	HPO:iea[2009-02-17]
OMIM:236730	Urofacial syndrome		HP:0000805	OMIM:236730	IEA					P	HPO:iea[2009-02-17]
OMIM:236730	Urofacial syndrome		HP:0001999	OMIM:236730	IEA					P	HPO:iea[2009-02-17]
OMIM:236730	Urofacial syndrome		HP:0000007	OMIM:236730	IEA					I	HPO:iea[2009-02-17]
OMIM:236730	Urofacial syndrome		HP:0000796	OMIM:236730	TAS					P	HPO:skoehler[2013-02-27]
OMIM:236730	Urofacial syndrome		HP:0002019	OMIM:236730	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236730	Urofacial syndrome		HP:0000028	OMIM:236730	IEA					P	HPO:iea[2009-02-17]
OMIM:236730	Urofacial syndrome		HP:0000126	OMIM:236730	IEA					P	HPO:iea[2009-02-17]
OMIM:604213	Chudley-Mccullough syndrome		HP:0006989	PMID:22578326	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0001321	PMID:22578326	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0002079	PMID:22578326	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0001250	PMID:22578326	PCS		2/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0002282	PMID:22578326	PCS		9/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0001270	PMID:22578326	PCS		5/12			P	HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0007033	PMID:22578326	PCS		8/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0100702	PMID:22578326	PCS		8/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0000007	PMID:22578326	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0000238	PMID:22578326	PCS		7/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0001338	PMID:22578326	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0002119	PMID:22578326	PCS		12/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0002700	PMID:22578326	PCS					P	HPO:skoehler[2012-11-19];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0002126	PMID:22578326	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-11-28]
OMIM:604213	Chudley-Mccullough syndrome		HP:0008625	PMID:22578326	PCS	HP:0011463	12/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-11-28]
OMIM:143465	Attention deficit-hyperactivity disorder		HP:0000752	OMIM:143465	IEA					P	HPO:iea[2009-02-17]
OMIM:143465	Attention deficit-hyperactivity disorder		HP:0007018	OMIM:143465	TAS					P	HPO:skoehler[2009-02-17]
OMIM:143465	Attention deficit-hyperactivity disorder		HP:0000006	OMIM:143465	IEA					I	HPO:iea[2009-02-17]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0005227	PMID:24440087	PCS		9/18			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0002671	OMIM:276300	IEA					P	HPO:iea[2009-02-17]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0001274	PMID:22692065	PCS		2/3			P	HPO:skoehler[2013-06-05];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0001010	PMID:24440087	PCS		3/18			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0002282	PMID:22692065	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0012539	PMID:22692065	PCS		1/3			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0001909	PMID:24440087	PCS		1/18			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0009592	PMID:24440087;PMID:22692065	PCS		11/13			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0033682	PMID:24440087	PCS		1/18			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0040274	PMID:24440087	PCS		2/18			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0033681	PMID:24440087	PCS		2/18			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0012174	PMID:24440087;PMID:22692065	PCS		10/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0040276	PMID:24440087	PCS		1/18			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0012190	PMID:22692065	PCS		2/3			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0000007	PMID:22692065	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0000997	PMID:24440087	PCS		3/18			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0002859	OMIM:276300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0007565	PMID:24440087;PMID:22692065	PCS		20/21			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0009732	PMID:24440087	PCS		1/18			P	HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0002888	OMIM:276300	IEA					P	HPO:iea[2009-02-17]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0002665	PMID:24440087	PCS		5/18			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0002885	PMID:24440087	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-27]
OMIM:276300	Mismatch repair cancer syndrome 1		HP:0003006	OMIM:276300	IEA					P	HPO:iea[2009-02-17]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0007957	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0003577	PMID:26320891	PCS		8/8			C	HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000486	PMID:26320891	PCS		2/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000122	OMIM:616603	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0010648	PMID:26320891	PCS		8/8			P	HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001252	PMID:26320891	PCS		7/7			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0100790	PMID:26320891	PCS		6/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000938	PMID:26320891	PCS		3/7			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0011220	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000519	PMID:26320891	PCS		6/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0004938	PMID:26320891	PCS		4/8			P	HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000337	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0008897	PMID:26320891	PCS		7/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000411	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001348	PMID:26320891	PCS		3/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000973	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0002677	PMID:26320891	PCS		2/8			P	HPO:skoehler[2015-11-15]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0005667	PMID:26320891	PCS		1/8			P	HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000252	PMID:26320891	PCS		5/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001762	PMID:26320891	PCS		3/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0011968	PMID:26320891	PCS		5/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001382	PMID:26320891	PCS		8/8			P	HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000270	PMID:26320891	PCS		4/7			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001263	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001181	PMID:26320891	PCS		5/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0100678	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0100857	PMID:26320891	PCS		1/8			P	HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000729	PMID:26320891	PCS		1/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0002827	PMID:26320891	PCS		5/7			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001659	OMIM:616603	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0001511	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0002645	PMID:26320891	PCS		2/7			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000006	PMID:26320891	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-07]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000369	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15]
OMIM:616603	Cutis laxa, autosomal dominant 3		HP:0000325	PMID:26320891	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-07]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0002014	OMIM:601419	TAS					P	HPO:iea[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0010628	OMIM:601419	IEA					P	HPO:iea[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0001662	PMID:17221859	PCS		1/7			P	HP:probinson[2019-01-26]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0001283	OMIM:601419	IEA					P	HPO:iea[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0003694	OMIM:601419	IEA					P	HPO:iea[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0003581	PMID:17221859	IEA		6/7			C	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0002460	OMIM:601419	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0001709	PMID:17221859	PCS		2/7			P	HP:probinson[2019-01-26]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0001639	PMID:17221859	PCS		2/7			P	HPO:iea[2009-02-17];HP:probinson[2019-01-26]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0000007	PMID:9697706	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-01-26]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0001723	PMID:17221859	PCS		1/7			P	HP:probinson[2019-01-26]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0002747	PMID:17221859	PCS		1/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-15]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0002019	OMIM:601419	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0000006	PMID:17221859	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-01-26]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0001644	PMID:17221859	PCS		1/7			P	HPO:skoehler[2012-10-17];HP:probinson[2019-01-26]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0003458	OMIM:601419	IEA					P	HPO:iea[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0002600	OMIM:601419	IEA					P	HPO:iea[2009-02-17]
OMIM:601419	Myopathy, myofibrillar, 1		HP:0000467	OMIM:601419	IEA					P	HPO:iea[2009-02-17]
OMIM:619256	Hypercholanemia, familial 2		HP:0100512	PMID:28835676	PCS		8/8			P	HPO:probinson[2021-06-20]
OMIM:619256	Hypercholanemia, familial 2		HP:0008282	PMID:24867799	PCS		0/2			P	HPO:probinson[2021-06-20];HPO:probinson[2022-07-10]
OMIM:619256	Hypercholanemia, familial 2		HP:0000938	PMID:28835676	PCS		3/8			P	HPO:probinson[2021-06-20]
OMIM:619256	Hypercholanemia, familial 2		HP:0000007	PMID:28835676	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619256	Hypercholanemia, familial 2		HP:0012202	PMID:24867799;PMID:28835676	PCS		10/10			P	HPO:probinson[2021-06-20]
OMIM:619256	Hypercholanemia, familial 2		HP:0006579	PMID:24867799	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619256	Hypercholanemia, familial 2		HP:0003623	PMID:24867799	PCS		2/2			C	HPO:probinson[2021-06-20]
OMIM:616165	Nemaline myopathy 10		HP:0003202	PMID:25250574	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0010628	PMID:25250574	PCS		2/2			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0003324	PMID:25250574	PCS		21/21			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001561	PMID:25250574	PCS		13/21			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0003577	PMID:25250574	PCS		21/21			C	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001283	PMID:25250574	PCS		2/2			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001371	PMID:25250574	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0011968	PMID:25250574	PCS		21/21			P	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0006829	PMID:25250574	PCS	HP:0003623	21/21			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001290	PMID:25250574	PCS		21/21			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0012548	PMID:25250574	PCS		11/11			P	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0000602	PMID:25250574	PCS		6/21			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0002803	PMID:25250574	PCS		6/21			P	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0000007	PMID:25250574	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001558	PMID:25250574	PCS		9/21			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0002747	PMID:25250574	PCS		21/21			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001324	PMID:25250574	PCS		21/21		HP:0012837	P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0003811	PMID:25250574	PCS		7/21			C	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001522	PMID:25250574	PCS		6/21			C	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001623	PMID:25250574	PCS		4/21			P	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0003798	PMID:25250574	PCS		11/11			P	HPO:probinson[2023-01-23]
OMIM:616165	Nemaline myopathy 10		HP:0001622	PMID:25250574	PCS		7/21			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-01-23]
OMIM:618148	Extraoral halitosis due to MTO deficiency		HP:0003577	PMID:29255262	PCS		2/4			C	HPO:probinson[2022-06-24]
OMIM:618148	Extraoral halitosis due to MTO deficiency		HP:0025708	PMID:29255262	PCS		1/4			C	HPO:probinson[2022-06-24]
OMIM:618148	Extraoral halitosis due to MTO deficiency		HP:0100812	PMID:29255262	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-24]
OMIM:618148	Extraoral halitosis due to MTO deficiency		HP:0003593	PMID:29255262	PCS		1/4			C	HPO:probinson[2022-06-24]
OMIM:618148	Extraoral halitosis due to MTO deficiency		HP:0000007	PMID:29255262	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-24]
OMIM:620158	Spinocerebellar ataxia 50		HP:0002345	PMID:34788392	PCS		1/17			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0003596	PMID:34788392	PCS		15/17			C	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0000651	PMID:34788392	PCS		3/16			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0000365	PMID:34788392	PCS		3/17			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0002354	PMID:34788392	PCS		1/16			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0002186	PMID:34788392	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0001272	PMID:34788392	PCS		5/12			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0003584	PMID:34788392	PCS		1/17			C	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0001251	PMID:34788392	PCS		17/17			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0002174	PMID:34788392	PCS		1/17			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0002072	PMID:34788392	PCS		1/17			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0033051	PMID:34788392	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0000639	PMID:34788392	PCS		13/16			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0011462	PMID:34788392	PCS		1/17			C	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0032121	PMID:34788392	PCS		1/17			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0000508	PMID:34788392	PCS		2/16			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0000006	PMID:34788392	PCS					I	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0002346	PMID:34788392	PCS		1/17			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0006855	PMID:34788392	PCS		3/12			P	HPO:probinson[2023-03-04]
OMIM:620158	Spinocerebellar ataxia 50		HP:0001336	PMID:34788392	PCS		4/17			P	HPO:probinson[2023-03-04]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0002257	PMID:27486780	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0001696	PMID:27486780	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0002110	PMID:27486780	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0033036	PMID:27486780	PCS		3/3			P	HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0100582	PMID:27486780	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0031245	PMID:27486780	PCS		3/3			P	HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0031565	PMID:27486780	PCS		1/3			P	HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0011109	PMID:27486780	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0000007	PMID:27486780	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0006532	PMID:27486780	PCS		3/3			P	HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0000389	PMID:27486780	PCS		3/3			P	HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0002643	PMID:27486780	PCS		1/3			P	HPO:probinson[2023-03-07]
OMIM:617092	Ciliary dyskinesia, primary, 35		HP:0003623	PMID:27486780	PCS		3/3			C	HPO:probinson[2023-03-07]
OMIM:107970	Arrhythmogenic right ventricular dysplasia, familial, 1		HP:0003621	PMID:15639475	PCS		3/3			C	HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:107970	Arrhythmogenic right ventricular dysplasia, familial, 1		HP:0011663	PMID:15639475	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-07-10]
OMIM:107970	Arrhythmogenic right ventricular dysplasia, familial, 1		HP:0004308	PMID:15639475	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:107970	Arrhythmogenic right ventricular dysplasia, familial, 1		HP:0000006	PMID:15639475	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:107970	Arrhythmogenic right ventricular dysplasia, familial, 1		HP:0001645	PMID:15639475	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0002983	PMID:28191891	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-Micromelia syndrome		HP:0003577	PMID:28191891	PCS					C	HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0002089	OMIM:251230	IEA					P	HPO:skoehler[2019-04-18]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000160	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0012745	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0009821	PMID:28191891	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000774	OMIM:251230	IEA					P	HPO:skoehler[2019-04-18]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000476	OMIM:251230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0001562	OMIM:251230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0002410	PMID:28191891	PCS					P	HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000175	OMIM:251230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0001363	PMID:28191891	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000252	PMID:28191891	PCS	HP:0030674	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0001762	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000470	PMID:28191891	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0003041	OMIM:251230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0012165	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0007370	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000921	PMID:28191891	PCS					P	HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000007	PMID:28191891	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000568	OMIM:251230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0009777	PMID:28191891	PCS					P	HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000444	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0001511	PMID:28191891	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0003811	PMID:28191891	PCS					C	HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0005736	OMIM:251230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0003974	OMIM:251230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000369	PMID:28191891	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000347	PMID:28191891	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0009879	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:251230	Microcephaly-micromelia syndrome		HP:0000445	PMID:28191891	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:155950	Melorheostosis, isolated		HP:0003676	OMIM:155950	TAS					C	HPO:skoehler[2012-10-17]
OMIM:155950	Melorheostosis, isolated		HP:0100774	OMIM:155950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:155950	Melorheostosis, isolated		HP:6000817	OMIM:155950	TAS					P	HPO:probinson[2024-08-03]
OMIM:155950	Melorheostosis, isolated		HP:0011001	OMIM:155950	IEA					P	HPO:iea[2009-02-17]
OMIM:155950	Melorheostosis, isolated		HP:0003745	OMIM:155950	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0007083	PMID:24482476	PCS		2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0002540	PMID:24482476	PCS	HP:0011463	2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0011463	PMID:24482476	PCS		2/2			C	HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0007178	PMID:24482476	PCS		2/2			P	HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0000007	PMID:24482476	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0012407	PMID:24482476	PCS	HP:0011463	2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0001258	PMID:24482476	PCS					P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0000763	PMID:24482476	PCS		2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0001257	PMID:24482476	PCS		2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0003438	PMID:24482476	PCS		2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615685	Spastic paraplegia 61, autosomal recessive		HP:0001249	PMID:24482476	PCS		0/2			P	HPO:probinson[2022-04-11]
OMIM:615849	Culler-Jones syndrome		HP:0000054	OMIM:615849	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0000175	OMIM:615849	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0010627	OMIM:615849	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0004322	OMIM:615849	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0001263	OMIM:615849	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0011755	OMIM:615849	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0011800	OMIM:615849	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0040075	OMIM:615849	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615849	Culler-Jones syndrome		HP:0100259	OMIM:615849	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0003828	OMIM:615849	TAS					M	HPO:skoehler[2015-12-30]
OMIM:615849	Culler-Jones syndrome		HP:0003829	OMIM:615849	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615849	Culler-Jones syndrome		HP:0000601	OMIM:615849	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0000873	OMIM:615849	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0000135	OMIM:615849	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615849	Culler-Jones syndrome		HP:0000028	OMIM:615849	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0000204	OMIM:615849	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:615849	Culler-Jones syndrome		HP:0000006	OMIM:615849	TAS					I	HPO:skoehler[2015-12-30]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0002014	OMIM:211600	IEA					P	HPO:iea[2009-02-17]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0002630	OMIM:211600	TAS					P	HPO:probinson[2012-07-16]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0003621	PMID:7912266	PCS		1/33			C	HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0004322	PMID:7912266	PCS		31/33			P	HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0001394	OMIM:211600	IEA					P	HPO:iea[2009-02-17]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0002240	PMID:7912266	PCS		32/33			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0003593	PMID:7912266	PCS		32/33			C	HPO:iea[2009-02-17];HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0001081	PMID:7912266	PCS		10/31			P	HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0030828	PMID:7912266	PCS		10/31			P	HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0002908	PMID:7912266	PCS		33/33			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0001508	OMIM:211600	IEA					P	HPO:iea[2009-02-17]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0000938	PMID:7912266	PCS		2/33			P	HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0002748	PMID:7912266	PCS		25/33			P	HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0000007	PMID:9500542	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0006575	OMIM:211600	IEA					P	HPO:iea[2009-02-17]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0000989	PMID:7912266	PCS		32/33			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0000421	PMID:7912266	PCS		17/31			P	HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0000952	PMID:7912266	PCS		33/33			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-09]
OMIM:211600	Cholestasis, progressive familial intrahepatic 1		HP:0001744	PMID:7912266	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-10-09]
OMIM:616398	Dystonia 26, myoclonic		HP:0000473	PMID:25983243	PCS		5/8			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0003676	PMID:25983243	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0003621	PMID:25983243	PCS		5/8			C	HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0001332	PMID:25983243	PCS		7/8			P	HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0001260	PMID:25983243	PCS		1/8			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0012049	PMID:25983243	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0025708	PMID:25983243	PCS		1/8			C	HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0001618	PMID:25983243	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0000716	PMID:25983243	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0011463	PMID:25983243	PCS		2/8			C	HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0000739	PMID:25983243	PCS		1/8			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0000006	PMID:25983243	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0000643	PMID:25983243	PCS		3/8			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-04]
OMIM:616398	Dystonia 26, myoclonic		HP:0001336	PMID:25983243	PCS		7/8			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-04]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0002521	PMID:26783368	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0003676	PMID:26783368	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0002540	OMIM:617086	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001272	PMID:26783368	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001250	PMID:26783368	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001252	PMID:26783368	PCS		3/3			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0003593	PMID:26783368	PCS		4/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001270	PMID:26783368	PCS		4/4			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001324	PMID:26783368	PCS		3/3			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001347	PMID:26783368	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0002015	PMID:26783368	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001344	PMID:26783368	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0002376	PMID:26783368	PCS		3/3			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001263	OMIM:617086	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0005484	PMID:26783368	PCS		4/4			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0011097	PMID:26783368	PCS		2/4			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0003819	PMID:26783368	PCS		1/4			C	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0009830	OMIM:617086	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0000007	PMID:22499341	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0000648	OMIM:617086	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0000505	PMID:26783368	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0000543	PMID:26783368	PCS		3/4			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001257	PMID:26783368	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0001510	PMID:26783368	PCS		1/3			P	HPO:probinson[2022-10-23]
OMIM:617086	Encephalopathy due to defective mitochondrial and peroxisomal fission 2		HP:0000544	PMID:26783368	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities		HP:0001000	OMIM:300719	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities		HP:0000365	OMIM:300719	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities		HP:0000518	OMIM:300719	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities		HP:0001419	OMIM:300719	TAS					I	HPO:skoehler[2012-11-20]
OMIM:300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities		HP:0000789	OMIM:300719	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300719	Deafness, cataract, retinitis pigmentosa, and sperm abnormalities		HP:0000510	OMIM:300719	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0003621	PMID:11891693	PCS		7/7			C	HPO:probinson[2009-02-17];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0003795	PMID:11891693	PCS					P	HPO:probinson[2013-12-20];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0002750	PMID:11891693	PCS		0/7			P	HPO:probinson[2013-12-20];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0005872	PMID:11891693	PCS		7/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0005819	PMID:11891693	PCS					P	HPO:probinson[2013-12-20];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0009882	PMID:11891693	PCS					P	HPO:probinson[2013-12-20];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0003040	PMID:11891693	PCS		7/7			P	HPO:skoehler[2015-01-27];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0009466	OMIM:606835	TAS					P	HPO:probinson[2009-02-17]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0001857	PMID:11891693	PCS					P	HPO:probinson[2013-12-20];HPO:probinson[2024-03-10]
OMIM:606835	Digital arthropathy-brachydactyly, familial		HP:0000006	PMID:21964574	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-10]
OMIM:611391	Cataract 33, multiple types		HP:0100018	OMIM:611391	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611391	Cataract 33, multiple types		HP:0003621	PMID:17225135	PCS		10/11			C	HPO:probinson[2022-11-08]
OMIM:611391	Cataract 33, multiple types		HP:0011463	PMID:17225135	PCS		1/11			C	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:611391	Cataract 33, multiple types		HP:0100019	PMID:17225135	PCS	HP:0003621	3/3			P	HPO:probinson[2013-04-01];HPO:probinson[2022-11-08]
OMIM:611391	Cataract 33, multiple types		HP:0000007	OMIM:611391	TAS					I	HPO:probinson[2013-01-09]
OMIM:611391	Cataract 33, multiple types		HP:0007971	OMIM:611391	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611391	Cataract 33, multiple types		HP:0000006	PMID:17225135	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:215300	Chondrosarcoma		HP:0001442	OMIM:215300	TAS					I	HPO:probinson[2020-11-26]
OMIM:215300	Chondrosarcoma		HP:0006765	OMIM:215300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0002015	PMID:29466837	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0002521	PMID:29466837	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0000252	PMID:29466837	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0002510	PMID:29466837	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0001344	PMID:29466837	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0002540	PMID:29466837	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0002079	PMID:29466837	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0001250	PMID:29466837	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0001263	PMID:29466837	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0003593	PMID:29466837	PCS		2/6			C	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0001290	PMID:29466837	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0011471	PMID:29466837	PCS		1/6			P	HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0001508	PMID:29466837	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0100704	PMID:29466837	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0011463	PMID:29466837	PCS		1/6			C	HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0200134	PMID:29466837	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0002500	PMID:29466837	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0000006	PMID:29466837	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0002126	PMID:29466837	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617938	Developmental and epileptic encephalopathy 62		HP:0003623	PMID:29466837	PCS		3/6			C	HPO:probinson[2021-02-18]
OMIM:258200	Oliver syndrome		HP:0001162	OMIM:258200	IEA					P	HPO:iea[2009-02-17]
OMIM:258200	Oliver syndrome		HP:0000007	OMIM:258200	IEA					I	HPO:iea[2009-02-17]
OMIM:258200	Oliver syndrome		HP:0001249	OMIM:258200	IEA					P	HPO:iea[2009-02-17]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001892	PMID:9312170	PCS					P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001872	PMID:17185466	PCS		HP:0040282			P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0002240	OMIM:612840	TAS					P	HPO:skoehler[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0003593	OMIM:612840	TAS					C	HPO:skoehler[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001581	PMID:17185466	PCS					P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001482	PMID:17185466	PCS					P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0012531	PMID:17185466	PCS					P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0011002	OMIM:612840	TAS		HP:0040283			P	HPO:skoehler[2015-03-22]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001903	OMIM:612840	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0002718	PMID:9312170	PCS	HP:0003593	HP:0040282			P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0100806	PMID:17185466	PCS					P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0000007	OMIM:612840	TAS					I	HPO:skoehler[2010-06-19]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0000967	OMIM:612840	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001978	PMID:17185466	PCS		HP:0040284			P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0002733	PMID:17185466	PCS					P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0000421	PMID:17185466	PCS		HP:0040283			P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001433	PMID:17185466	PCS		HP:0040282			P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001744	PMID:17185466	PCS		HP:0040282			P	HPO:lccarmody[2017-06-21]
OMIM:612840	Leukocyte adhesion deficiency, type III		HP:0001974	PMID:9312170	PCS					P	HPO:lccarmody[2017-06-21]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0003774	PMID:15879175	PCS					P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-17]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0000100	OMIM:603965	TAS					P	HPO:skoehler[2013-01-10]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0000097	OMIM:603965	TAS					P	HPO:skoehler[2013-01-09]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0011462	PMID:15879175	PCS					C	HPO:probinson[2023-02-17]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0000822	OMIM:603965	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0000093	PMID:15879175	PCS					P	HPO:skoehler[2013-01-10];HPO:probinson[2023-02-17]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0012622	OMIM:603965	TAS					P	HPO:probinson[2014-01-18]
OMIM:603965	Focal segmental glomerulosclerosis 2		HP:0000006	PMID:15879175	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:210250	Sitosterolemia 1		HP:0004446	PMID:25110228	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0001892	OMIM:210250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210250	Sitosterolemia 1		HP:0031290	OMIM:210250	IEA					P	HPO:skoehler[2019-09-07]
OMIM:210250	Sitosterolemia 1		HP:0100546	PMID:25110228	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0001903	PMID:25110228	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0008158	OMIM:210250	IEA					P	HPO:iea[2009-02-17]
OMIM:210250	Sitosterolemia 1		HP:0001902	PMID:25110228	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0001923	PMID:25110228	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0025435	PMID:25110228	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0001744	PMID:25110228	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0001369	OMIM:210250	IEA					P	HPO:iea[2009-02-17]
OMIM:210250	Sitosterolemia 1		HP:0020181	PMID:25110228	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0003124	PMID:25110228	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0003540	OMIM:210250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:210250	Sitosterolemia 1		HP:0001084	PMID:25110228	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0004870	OMIM:210250	IEA					P	HPO:iea[2009-02-17]
OMIM:210250	Sitosterolemia 1		HP:0003581	PMID:25110228	PCS		1/1			C	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0033341	OMIM:210250	TAS					P	HPO:probinson[2020-12-07]
OMIM:210250	Sitosterolemia 1		HP:0002829	OMIM:210250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210250	Sitosterolemia 1		HP:0000007	PMID:11099417	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0004802	OMIM:210250	IEA					P	HPO:iea[2009-02-17]
OMIM:210250	Sitosterolemia 1		HP:0001114	PMID:25110228	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0001873	PMID:25110228	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:210250	Sitosterolemia 1		HP:0002027	OMIM:210250	IEA					P	HPO:skoehler[2010-06-18]
OMIM:210250	Sitosterolemia 1		HP:0001677	PMID:25110228	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:612868	Corneal dystrophy, posterior amorphous		HP:0000540	OMIM:612868	TAS					P	HPO:skoehler[2014-02-06]
OMIM:612868	Corneal dystrophy, posterior amorphous		HP:0009918	OMIM:612868	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612868	Corneal dystrophy, posterior amorphous		HP:0001131	OMIM:612868	IEA					P	HPO:skoehler[2015-01-19]
OMIM:612868	Corneal dystrophy, posterior amorphous		HP:0003680	OMIM:612868	TAS					C	HPO:skoehler[2017-07-13]
OMIM:612868	Corneal dystrophy, posterior amorphous		HP:0003593	OMIM:612868	TAS					C	HPO:skoehler[2014-02-06]
OMIM:612868	Corneal dystrophy, posterior amorphous		HP:0000612	OMIM:612868	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612868	Corneal dystrophy, posterior amorphous		HP:0000006	OMIM:612868	TAS					I	HPO:skoehler[2014-02-06]
OMIM:615861	Familial idiopathic steroid-resistant nephrotic syndrome		HP:0000100	PMID:24814193	PCS	HP:0011463	4/4			P	HPO:probinson[2018-06-06]
OMIM:615861	Familial idiopathic steroid-resistant nephrotic syndrome		HP:0000007	PMID:24814193	PCS					I	HPO:skoehler[2017-07-13]
OMIM:615861	Familial idiopathic steroid-resistant nephrotic syndrome		HP:0031266	PMID:24814193	PCS	HP:0011463				P	HPO:probinson[2018-06-06]
OMIM:615861	Familial idiopathic steroid-resistant nephrotic syndrome		HP:0012588	PMID:24814193	PCS	HP:0011463	1/4			P	HPO:skoehler[2015-01-27]
OMIM:615861	Familial idiopathic steroid-resistant nephrotic syndrome		HP:0012579	PMID:24814193	PCS	HP:0011463	1/1			P	HPO:skoehler[2017-07-13]
OMIM:259650	Osteoma of middle ear		HP:0100246	OMIM:259650	IEA					P	HPO:skoehler[2015-01-27]
OMIM:259650	Osteoma of middle ear		HP:0000007	OMIM:259650	IEA					I	HPO:iea[2009-02-17]
OMIM:259650	Osteoma of middle ear		HP:0000598	OMIM:259650	IEA					P	HPO:iea[2009-02-17]
OMIM:619083	Delpire-Mcneill syndrome		HP:0002575	PMID:32658972	PCS		1/6			P	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0001276	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0002015	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0001344	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0000750	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0008619	PMID:32658972	PCS		2/6			P	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0031936	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0001263	PMID:32658972	PCS		6/6			P	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0001274	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0001290	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0001629	PMID:32658972	PCS		1/6			P	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0002827	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0000729	PMID:32658972	PCS		3/6			P	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0002539	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0001257	PMID:32658972	PCS					P	HPO:probinson[2020-12-15]
OMIM:619083	Delpire-Mcneill syndrome		HP:0000006	PMID:32658972	PCS					I	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:620602	Lymphatic malformation 14		HP:0001004	PMID:36928819	PCS					P	HPO:probinson[2024-03-12]
OMIM:620602	Lymphatic malformation 14		HP:0000006	PMID:36928819	PCS					I	HPO:probinson[2024-03-12]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0000131	PMID:15937070	PCS		22/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0002891	OMIM:150800	IEA					P	HPO:iea[2009-02-17]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0005584	PMID:15937070	PCS		20/46			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-03-23]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0003829	OMIM:150800	TAS					I	HPO:skoehler[2012-10-17]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0007620	OMIM:150800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0003536	OMIM:150800	IEA					P	HPO:iea[2009-02-17]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0000006	PMID:15937070	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0007437	PMID:15937070	PCS		16/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:150800	Hereditary leiomyomatosis and renal cell cancer		HP:0006755	OMIM:150800	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609284	Nemaline myopathy 1		HP:0000275	OMIM:609284	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609284	Nemaline myopathy 1		HP:0003621	OMIM:609284	IEA					C	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0003324	OMIM:609284	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0002015	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0002650	OMIM:609284	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609284	Nemaline myopathy 1		HP:0001761	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0000276	OMIM:609284	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609284	Nemaline myopathy 1		HP:0001371	OMIM:609284	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609284	Nemaline myopathy 1		HP:0001270	OMIM:609284	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0002093	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0009053	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0000767	OMIM:609284	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609284	Nemaline myopathy 1		HP:0001349	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0000007	OMIM:609284	IEA					I	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0000218	OMIM:609284	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609284	Nemaline myopathy 1		HP:0003701	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0003724	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0003798	OMIM:609284	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609284	Nemaline myopathy 1		HP:0000006	OMIM:609284	IEA					I	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0000467	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0003458	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:609284	Nemaline myopathy 1		HP:0008944	OMIM:609284	IEA					P	HPO:iea[2009-02-17]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0100743	PMID:15340263	PCS					P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0003003	PMID:16000562	PCS	HP:0003621	1/2			P	HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0009592	PMID:16283678	PCS		1/2			P	HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0012174	PMID:16000562	PCS	HP:0003621	1/2			P	HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0012174	PMID:16283678	PCS		1/2			P	HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0012190	PMID:16283678	PCS		1/2			P	HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0000007	PMID:15340263	PCS					I	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0000997	PMID:16000562	PCS		2/2			P	HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0007565	PMID:16000562;PMID:17557300;PMID:16283678;PMID:15340263	PCS		6/6			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0002665	PMID:16000562	PCS	HP:0011463	1/2			P	HPO:probinson[2021-01-01]
OMIM:619097	Mismatch repair cancer syndrome 3		HP:0009737	PMID:17557300	PCS		1/1			P	HPO:probinson[2021-01-01]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0000494	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0001883	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0001838	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0000470	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0007430	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0000007	PMID:19261599	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0001989	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0010557	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:618389	Fetal akinesia deformation sequence 3		HP:0000347	PMID:19261599	PCS					P	HPO:probinson[2020-06-27]
OMIM:123150	Jackson-Weiss syndrome		HP:0001363	OMIM:123150	IEA					P	HPO:iea[2009-02-17]
OMIM:123150	Jackson-Weiss syndrome		HP:0001783	OMIM:123150	TAS					P	HPO:probinson[2012-05-08]
OMIM:123150	Jackson-Weiss syndrome		HP:0004440	PMID:11343323	PCS		1/6			P	HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0000272	OMIM:123150	IEA					P	HPO:iea[2009-02-17]
OMIM:123150	Jackson-Weiss syndrome		HP:0004691	PMID:11343323	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0011800	PMID:11343323	PCS		1/6		HP:0012825	P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0010068	PMID:11343323	PCS		5/6			P	HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0008080	PMID:11343323	PCS		1/6			P	HPO:probinson[2012-06-08];HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0010105	PMID:11343323	PCS		2/6			P	HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0010077	PMID:11343323	PCS		4/6			P	HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0010055	OMIM:123150	TAS					P	HPO:probinson[2012-06-08]
OMIM:123150	Jackson-Weiss syndrome		HP:0011220	PMID:11343323	PCS		1/6			P	HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0010086	PMID:11343323	PCS		2/6			P	HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0008122	PMID:11343323	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0000520	PMID:11343323	PCS		1/6		HP:0012825	P	HPO:probinson[2023-01-30]
OMIM:123150	Jackson-Weiss syndrome		HP:0000006	OMIM:123150	IEA					I	HPO:iea[2009-02-17]
OMIM:620170	Spermatogenic failure 78		HP:0003251	PMID:36321563	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:620170	Spermatogenic failure 78		HP:0011462	PMID:36321563	PCS		2/2			C	HPO:probinson[2023-03-04]
OMIM:620170	Spermatogenic failure 78		HP:0032561	PMID:36321563	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:620170	Spermatogenic failure 78		HP:0032562	PMID:36321563	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:620170	Spermatogenic failure 78		HP:0000007	PMID:36321563	PCS					I	HPO:probinson[2023-03-04]
OMIM:620170	Spermatogenic failure 78		HP:0033712	PMID:36321563	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002421	PMID:25262651	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002069	PMID:25262651	PCS		1/2			P	HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002521	PMID:25262651	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0001344	PMID:25262651	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002540	PMID:25262651	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002650	OMIM:617904	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002266	PMID:25262651	PCS		1/2			P	HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002384	PMID:25262651	PCS		1/2			P	HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0003593	PMID:25262651	PCS		2/2			C	HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0001251	PMID:25262651	PCS		1/2		HP:0012825	P	HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0001290	PMID:25262651	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0010841	PMID:25262651	PCS		1/2			P	HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0012469	PMID:25262651	PCS		2/2			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0032792	PMID:25262651	PCS		1/2			P	HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0200134	PMID:25262651	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0100716	PMID:25262651	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002119	OMIM:617904	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0002307	OMIM:617904	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0000006	PMID:25262651	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617904	Epileptic encephalopathy, early infantile, 59		HP:0001249	PMID:25262651	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:192200	Varicose veins		HP:0002619	OMIM:192200	IEA					P	HPO:iea[2009-02-17]
OMIM:192200	Varicose veins		HP:0001426	PMID:4435791	TAS		50%			I	HPO:nvasilevsky[2019-03-12]
OMIM:192200	Varicose veins		HP:0001423	PMID:13561707	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000286	PMID:39419027	PCS		2/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000483	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000486	PMID:39419027	PCS		3/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000365	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0004322	PMID:39419027	PCS		3/21			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001250	PMID:39419027	PCS		13/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001252	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002020	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0004482	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0012745	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0003072	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0045075	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0010055	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000718	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0011220	PMID:39419027	PCS		3/30			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0012471	PMID:39419027	PCS		3/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000316	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000998	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000713	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000358	PMID:39419027	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001249	PMID:39419027	PCS		14/14			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000252	PMID:39419027	PCS		0/23			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001385	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000494	PMID:39419027	PCS		4/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002353	PMID:39419027	PCS		7/14			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002032	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001382	PMID:39419027	PCS		2/26			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000490	PMID:39419027	PCS		3/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001263	PMID:39419027	PCS		29/30			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0012775	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0030822	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000807	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000729	PMID:39419027	PCS		30/31			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000448	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000568	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000527	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000400	PMID:39419027	PCS		3/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000322	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000047	PMID:39419027	PCS		2/24			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002943	PMID:39419027	PCS		2/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000289	PMID:39419027	PCS		2/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000369	PMID:39419027	PCS		2/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000006	PMID:39419027	PCS					I	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000343	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000540	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002002	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002761	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000463	PMID:39419027	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0011039	PMID:39419027	PCS		4/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0005274	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001270	PMID:39419027	PCS		18/29			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0010865	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0100785	PMID:39419027	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000739	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0012450	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000414	PMID:39419027	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000337	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000733	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000417	PMID:39419027	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000411	PMID:39419027	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001269	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000256	PMID:39419027	PCS		0/22			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001741	PMID:39419027	PCS		1/26			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001348	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000396	PMID:39419027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000275	PMID:39419027	PCS		3/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000431	PMID:39419027	PCS		3/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000750	PMID:39419027	PCS		31/31			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002572	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000391	PMID:39419027	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0010535	PMID:39419027	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0002808	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000506	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000508	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0034332	PMID:39419027	PCS		8/21			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000821	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000348	PMID:39419027	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0001159	PMID:39419027	PCS		1/27			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000664	PMID:39419027	PCS		1/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0007018	PMID:39419027	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000421	PMID:39419027	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621285	Intellectual developmental disorder, autosomal dominant 76		HP:0000545	PMID:39419027	PCS		2/28			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0003676	OMIM:618404	IEA					C	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001310	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001332	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001250	PMID:30620337	PCS		12/19			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001272	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001371	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0000639	PMID:30620337	PCS	HP:0003593	12/19			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001508	PMID:30620337	PCS		12/18			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0040131	PMID:30620337	PCS		5/12			P	HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0003828	OMIM:618404	IEA					M	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0007366	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0002518	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0007108	OMIM:618404	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0002510	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001344	PMID:30620337	PCS		13/19			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0000750	PMID:30620337	PCS		19/19			P	HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0002650	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0003487	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0011968	PMID:30620337	PCS					P	HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001260	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001263	PMID:30620337	PCS		19/19			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0005484	PMID:30620337	PCS		3/17			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0002191	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0011344	OMIM:618404	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0011471	PMID:30620337	PCS		8/19			P	HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0000007	PMID:30620337	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0001257	PMID:30620337	PCS	HP:0003593	18/19			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618404	Leukodystrophy, hypomyelinating, 18		HP:0000762	OMIM:618404	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:116100	Cataract 20, multiple types		HP:0003621	PMID:18587492;PMID:16141006	PCS		18/18			C	HPO:probinson[2023-03-01]
OMIM:116100	Cataract 20, multiple types		HP:0100018	PMID:19262743	PCS	HP:0003577	7/7			P	HPO:probinson[2024-02-17]
OMIM:116100	Cataract 20, multiple types		HP:0100019	PMID:16141006	PCS		14/14			P	HPO:probinson[2023-03-01]
OMIM:116100	Cataract 20, multiple types		HP:0007971	PMID:18587492	PCS		4/4			P	HPO:probinson[2023-03-01]
OMIM:116100	Cataract 20, multiple types		HP:0010695	PMID:18587492	PCS		4/4			P	HPO:probinson[2023-03-01]
OMIM:116100	Cataract 20, multiple types		HP:0000006	PMID:16141006	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-01]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0003388	OMIM:615120	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0011463	PMID:19631309	PCS		2/2			C	HPO:probinson[2022-12-05]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0000508	PMID:19631309	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-05]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0009046	PMID:19631309	PCS		2/2			P	HPO:probinson[2022-12-05]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0000007	PMID:19631309	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-05]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0000218	OMIM:615120	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0002093	OMIM:615120	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0000774	OMIM:615120	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0003701	PMID:19631309	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-05]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0030319	PMID:19631309	PCS		2/2			P	HPO:probinson[2022-12-05]
OMIM:615120	Myasthenic syndrome, congenital, 8		HP:0003403	PMID:19631309	PCS		2/2			P	HPO:probinson[2022-12-05]
OMIM:613237	Glomerulosclerosis, focal segmental, 5		HP:0003774	PMID:20023659	PCS					P	HPO:probinson[2020-07-24]
OMIM:613237	Glomerulosclerosis, focal segmental, 5		HP:0002907	PMID:20023659	PCS					P	HPO:probinson[2020-07-24]
OMIM:613237	Glomerulosclerosis, focal segmental, 5		HP:0000097	PMID:20023659	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-24]
OMIM:613237	Glomerulosclerosis, focal segmental, 5		HP:0003581	PMID:20023659	PCS					C	HPO:probinson[2020-07-24]
OMIM:613237	Glomerulosclerosis, focal segmental, 5		HP:0000822	PMID:20023659	PCS					P	HPO:probinson[2020-07-24]
OMIM:613237	Glomerulosclerosis, focal segmental, 5		HP:0000093	PMID:20023659	PCS					P	HPO:probinson[2020-07-24]
OMIM:613237	Glomerulosclerosis, focal segmental, 5		HP:0000006	PMID:20023659	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2020-07-24]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0002069	PMID:24888894;PMID:22365152	PCS		4/8			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0003577	PMID:24888894	IEA		1/7			C	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0002121	PMID:24888894	PCS		1/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0001252	PMID:24888894	PCS		4/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0003593	PMID:25239001;PMID:24888894;PMID:22365152	PCS		7/9			C	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0010841	PMID:25239001	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0001270	PMID:24888894	PCS		6/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0011167	PMID:24888894	PCS		1/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0020221	PMID:25239001	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0001249	PMID:22365152	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0003623	PMID:24888894	PCS		1/7			C	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0000253	OMIM:614558	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0000252	PMID:25239001	PCS	HP:0011463	1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0002059	PMID:25239001;PMID:24888894	PCS		4/8			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0006813	PMID:24888894	PCS		1/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0002376	PMID:25239001;PMID:24888894;PMID:22365152	PCS		4/9			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0002373	PMID:24888894	PCS		1/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0001263	PMID:25239001;PMID:24888894;PMID:22365152	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0010850	PMID:22365152	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0011169	PMID:24888894	PCS		1/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0033258	PMID:22365152	PCS	HP:0003621	1/1			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0033258	PMID:24888894	PCS		0/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0011097	PMID:22365152	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0000729	PMID:22365152	PCS		1/1			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0032792	PMID:25239001;PMID:24888894	PCS		2/8			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0000722	PMID:22365152	PCS		1/1			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0200134	PMID:24888894	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0007334	PMID:24888894	PCS		1/7			P	HPO:probinson[2022-06-04]
OMIM:614558	Epileptic encephalopathy, early infantile, 13		HP:0000006	PMID:22365152	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-04]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000463	PMID:30580808	PCS		6/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000023	PMID:30580808	PCS		3/15			P	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0001250	PMID:30580808	PCS		4/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0001252	PMID:30580808	PCS		13/15			P	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0003593	PMID:30580808	PCS		15/15			C	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0033725	PMID:30580808	PCS		2/12			P	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0001508	PMID:30580808	PCS		6/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000718	PMID:30580808	PCS		10/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000998	PMID:30580808	PCS		6/15			P	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000219	PMID:30580808	PCS		6/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000752	PMID:30580808	PCS		10/15			P	HPO:skoehler[2019-04-18]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000179	PMID:30580808	PCS		5/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0001249	PMID:30580808	PCS		5/5			P	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0002059	PMID:30580808	PCS		2/12			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0001344	PMID:30580808	PCS		7/15			P	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000750	PMID:30580808	PCS		13/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0002650	PMID:30580808	PCS		5/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000574	PMID:30580808	PCS		6/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0011968	PMID:30580808	PCS		8/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0002033	PMID:30580808	PCS		8/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0001263	PMID:30580808	PCS		15/15			P	HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000508	PMID:30580808	PCS		5/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0002209	PMID:30580808	PCS		4/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000964	PMID:30580808	PCS		2/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000527	PMID:30580808	PCS		5/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0100716	PMID:30580808	PCS		10/15			P	HPO:skoehler[2019-04-18]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000006	PMID:30580808	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618362	Coffin-Siris syndrome 8		HP:0000028	PMID:30580808	PCS		2/12			P	HPO:probinson[2023-02-12]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0000252	PMID:27055666	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0002059	PMID:27055666	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0000486	PMID:27055666	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0001250	PMID:27055666	PCS		1/3			P	HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0001263	PMID:27055666	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0001252	PMID:27055666	PCS		1/3			P	HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0000592	PMID:27055666	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0003593	PMID:27055666	PCS		3/3			C	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0000280	PMID:27055666	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0012760	PMID:27055666	PCS		1/3			P	HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0100702	PMID:27055666	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0000007	PMID:27055666	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:617051	Neurodevelopmental disorder with microcephaly and gray sclerae		HP:0002119	PMID:27055666	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-16]
OMIM:620825	Immunodeficiency 119		HP:0004313	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0003453	PMID:30498080	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0030388	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0005387	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0032301	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0002090	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0011108	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0030318	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0031160	PMID:30498080	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0011463	PMID:30498080	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0000403	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0002837	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0001888	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0000007	PMID:30498080	PCS					I	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0410028	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0002863	PMID:30498080	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:620825	Immunodeficiency 119		HP:0001875	PMID:30498080	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-04]
OMIM:114065	Calcific aortic disease with immunologic abnormalities, familial		HP:0001650	OMIM:114065	IEA					P	HPO:iea[2009-02-17]
OMIM:114065	Calcific aortic disease with immunologic abnormalities, familial		HP:0001659	OMIM:114065	TAS					P	HPO:skoehler[2013-01-21]
OMIM:114065	Calcific aortic disease with immunologic abnormalities, familial		HP:0004380	PMID:8213448	PCS					P	HPO:probinson[2017-09-21]
OMIM:114065	Calcific aortic disease with immunologic abnormalities, familial		HP:0010702	OMIM:114065	IEA					P	HPO:iea[2009-02-17]
OMIM:114065	Calcific aortic disease with immunologic abnormalities, familial		HP:0000006	OMIM:114065	IEA					I	HPO:iea[2009-02-17]
OMIM:276880	Urocanase deficiency		HP:0002136	PMID:19304569	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0002345	PMID:19304569	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0002078	PMID:19304569	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0004322	OMIM:276880	IEA					P	HPO:iea[2009-02-17]
OMIM:276880	Urocanase deficiency		HP:0001310	PMID:19304569	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0002066	PMID:19304569	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0001251	PMID:19304569	PCS		1/1			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0012237	PMID:19304569	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0000639	PMID:19304569	PCS		1/1			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0011463	PMID:19304569	PCS		1/1			C	HPO:probinson[2022-11-06]
OMIM:276880	Urocanase deficiency		HP:0000718	OMIM:276880	TAS					P	HPO:probinson[2009-02-17]
OMIM:276880	Urocanase deficiency		HP:0000007	PMID:19304569	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:221700	Deafness, neural, with atypical atopic dermatitis		HP:0003212	OMIM:221700	TAS					P	HPO:probinson[2013-03-22]
OMIM:221700	Deafness, neural, with atypical atopic dermatitis		HP:0000407	OMIM:221700	TAS					P	HPO:skoehler[2010-06-18]
OMIM:221700	Deafness, neural, with atypical atopic dermatitis		HP:0007573	OMIM:221700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:221700	Deafness, neural, with atypical atopic dermatitis		HP:0000007	OMIM:221700	TAS					I	HPO:skoehler[2009-02-17]
DECIPHER:48	Early-onset Alzheimer disease with cerebral amyloid angiopathy		HP:0000726	DECIPHER:48	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:48	Early-onset Alzheimer disease with cerebral amyloid angiopathy		HP:0002185	DECIPHER:48	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:48	Early-onset Alzheimer disease with cerebral amyloid angiopathy		HP:0100256	DECIPHER:48	IEA					P	HPO:skoehler[2013-05-29]
OMIM:104510	Amelogenesis imperfecta, type IV		HP:0000705	PMID:15666299	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:104510	Amelogenesis imperfecta, type IV		HP:0006297	PMID:15666299	PCS		11/11			P	HPO:probinson[2021-07-05]
OMIM:104510	Amelogenesis imperfecta, type IV		HP:0006286	PMID:15666299	PCS		11/11			P	HPO:probinson[2021-07-05]
OMIM:104510	Amelogenesis imperfecta, type IV		HP:0000679	PMID:15666299	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:104510	Amelogenesis imperfecta, type IV		HP:0000006	PMID:15666299	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0007759	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0006824	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0007957	PMID:16380922	PCS		1/4			P	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001772	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000040	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000085	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0009380	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000518	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000957	OMIM:268300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0003826	OMIM:268300	TAS		HP:0040283			C	HPO:probinson[2012-03-16]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000316	PMID:16380922	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0007486	PMID:16380922	PCS		5/8			P	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0009466	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000238	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0008897	OMIM:268300	TAS					P	HPO:probinson[2012-03-16]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001643	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000113	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000476	OMIM:268300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000358	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001249	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000252	PMID:15821733	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000494	OMIM:268300	TAS					P	HPO:skoehler[2012-11-20]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000175	PMID:16380922	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0006380	PMID:16380922	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0008683	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000568	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000007	PMID:15821733	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0009777	PMID:16380922	PCS		4/7			P	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0006466	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0009933	OMIM:268300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000520	PMID:16380922	PCS		5/8			P	HPO:probinson[2012-03-16];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000047	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0002987	PMID:16380922	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0008846	OMIM:268300	TAS					P	HPO:probinson[2012-03-16]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000369	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000204	PMID:16380922	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000248	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0003577	PMID:16380922	PCS		8/8			C	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000387	OMIM:268300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001156	OMIM:268300	TAS					P	HPO:skoehler[2014-11-26]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0005792	PMID:16380922	PCS		4/8			P	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0008070	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001629	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000813	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000218	OMIM:268300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0030084	OMIM:268300	TAS					P	HPO:skoehler[2014-09-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001747	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000377	OMIM:268300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0030721	OMIM:268300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001561	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001363	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000431	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0009829	PMID:16380922	PCS		8/8			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000430	PMID:16380922	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0003982	PMID:16380922	PCS		3/8			P	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0003022	PMID:16380922	PCS		4/8			P	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000592	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000470	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000272	OMIM:268300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001080	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0007330	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0007452	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001239	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0430028	PMID:16380922	PCS		5/6			P	HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0005916	OMIM:268300	TAS					P	HPO:skoehler[2012-11-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0003616	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000625	OMIM:268300	TAS					P	HPO:probinson[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0008665	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001159	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000586	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0001631	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000347	PMID:16380922	PCS		3/7			P	HPO:probinson[2012-03-16];HPO:probinson[2023-02-21]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000028	OMIM:268300	IEA					P	HPO:iea[2009-02-17]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0000589	OMIM:268300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:268300	Roberts-SC phocomelia syndrome		HP:0003974	PMID:16380922	PCS		6/7			P	HPO:probinson[2023-02-21]
OMIM:615134	Melanoma, cutaneous malignant, susceptibility to, 9		HP:0002861	PMID:23348503	PCS					P	HPO:probinson[2015-09-03]
OMIM:615134	Melanoma, cutaneous malignant, susceptibility to, 9		HP:0000006	PMID:23348503	PCS					I	HPO:probinson[2015-09-03]
OMIM:225200	Ectopia lentis et pupillae		HP:0009917	PMID:20702823	PCS		2/10			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-28]
OMIM:225200	Ectopia lentis et pupillae		HP:0000541	PMID:20702823	PCS		1/10			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-28]
OMIM:225200	Ectopia lentis et pupillae		HP:0000518	PMID:20702823	PCS					P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-28]
OMIM:225200	Ectopia lentis et pupillae		HP:0009918	PMID:20702823	PCS		10/10			P	HPO:probinson[2023-02-28]
OMIM:225200	Ectopia lentis et pupillae		HP:0012805	PMID:20702823	PCS		5/10			P	HPO:probinson[2023-02-28]
OMIM:225200	Ectopia lentis et pupillae		HP:0000007	PMID:20702823	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:225200	Ectopia lentis et pupillae		HP:0001083	PMID:20702823	PCS		5/10			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-28]
OMIM:225200	Ectopia lentis et pupillae		HP:0011003	PMID:20702823	PCS		2/10			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-28]
OMIM:243185	Natal teeth - intestinal pseudoobstruction - patent ductus		HP:0000695	OMIM:243185	IEA					P	HPO:skoehler[2015-01-27]
OMIM:156530	Metatropic dysplasia		HP:0003037	PMID:20577006;PMID:19232556	PCS		24/24			P	HPO:probinson[2022-03-05];HPO:skoehler[2017-07-13];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003477	OMIM:156530	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:156530	Metatropic dysplasia		HP:0003510	OMIM:156530	TAS					P	HPO:probinson[2009-02-17]
OMIM:156530	Metatropic dysplasia		HP:0003311	PMID:19232556	PCS		1/1			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0001371	PMID:19232556	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0009381	OMIM:156530	TAS					P	HPO:skoehler[2014-11-26]
OMIM:156530	Metatropic dysplasia		HP:0034187	PMID:19232556	PCS		1/2			P	HPO:probinson[2022-04-15]
OMIM:156530	Metatropic dysplasia		HP:0002857	PMID:20577006	PCS		13/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002810	PMID:19232556	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002656	PMID:20577006	PCS		13/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003623	PMID:19232556	PCS		2/2			C	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002751	PMID:20577006	PCS		9/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003521	PMID:20577006	PCS		6/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002750	PMID:20577006	PCS		15/19			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003562	OMIM:156530	TAS					P	HPO:probinson[2009-02-17]
OMIM:156530	Metatropic dysplasia		HP:0000926	PMID:20577006;PMID:19232556	PCS		24/24			P	HPO:probinson[2022-03-05];HPO:skoehler[2012-10-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002825	PMID:20577006	PCS		12/22			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002869	PMID:20577006;PMID:19232556	PCS		23/24			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002826	PMID:19232556	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0000887	PMID:20577006	PCS		21/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003911	OMIM:156530	TAS					P	HPO:probinson[2012-06-10]
OMIM:156530	Metatropic dysplasia		HP:0002822	OMIM:156530	IEA					P	HPO:probinson[2009-02-17]
OMIM:156530	Metatropic dysplasia		HP:0000006	PMID:19232556	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003015	PMID:20577006	PCS		22/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003332	OMIM:156530	IEA					P	HPO:probinson[2009-02-17]
OMIM:156530	Metatropic dysplasia		HP:0001156	PMID:20577006;PMID:19232556	PCS		15/21			P	HPO:probinson[2022-03-05];HPO:skoehler[2015-04-05];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003375	PMID:19232556	PCS		2/2			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:6000653	PMID:28744080	PCS					P	HPO:probinson[2024-05-09]
OMIM:156530	Metatropic dysplasia		HP:0008873	PMID:20577006	PCS		16/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0006375	PMID:20577006	PCS		22/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002834	OMIM:156530	TAS					P	HPO:probinson[2012-06-10]
OMIM:156530	Metatropic dysplasia		HP:0002878	OMIM:156530	TAS					P	HPO:skoehler[2014-06-24]
OMIM:156530	Metatropic dysplasia		HP:0002879	OMIM:156530	TAS					P	HPO:probinson[2009-02-17]
OMIM:156530	Metatropic dysplasia		HP:0001989	OMIM:156530	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:156530	Metatropic dysplasia		HP:0000774	PMID:20577006	PCS		20/22			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0000773	PMID:20577006	PCS		21/22			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002831	OMIM:156530	TAS					P	HPO:probinson[2009-02-17]
OMIM:156530	Metatropic dysplasia		HP:0002650	PMID:19232556	PCS	HP:0003577	2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002650	PMID:20577006	PCS		5/22			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003025	PMID:20577006	PCS		7/21			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002093	PMID:19232556	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0005280	PMID:19232556	PCS		1/2			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0003180	PMID:19232556	PCS		1/2			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0010579	PMID:19232556	PCS		2/2			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002808	PMID:20577006	PCS		6/22			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0000904	PMID:19232556	PCS		2/2			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002804	OMIM:156530	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:156530	Metatropic dysplasia		HP:0001558	OMIM:156530	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:156530	Metatropic dysplasia		HP:0000348	PMID:19232556	PCS		2/2			P	HPO:probinson[2022-03-05]
OMIM:156530	Metatropic dysplasia		HP:0002766	OMIM:156530	TAS					P	HPO:probinson[2009-02-17]
OMIM:156530	Metatropic dysplasia		HP:0003336	OMIM:156530	TAS		20/20			P	HPO:probinson[2009-02-17]
OMIM:618410	Deafness, autosomal recessive 113		HP:0003621	PMID:29703829	PCS		7/7			C	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:618410	Deafness, autosomal recessive 113		HP:0001751	PMID:29703829	PCS		0/7			P	HPO:probinson[2019-07-07];HPO:probinson[2024-03-15]
OMIM:618410	Deafness, autosomal recessive 113		HP:0000407	PMID:29703829	PCS	HP:0003621	7/7			P	HPO:probinson[2019-07-07]
OMIM:618410	Deafness, autosomal recessive 113		HP:0000007	PMID:29703829	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:614202	Rafiq syndrome		HP:0004523	PMID:21763484	PCS		3/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000486	PMID:24566669	PCS		5/12			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0004322	PMID:24566669	PCS		3/12			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001250	PMID:24566669;PMID:24348268;PMID:21763484	PCS		6/31			P	HPO:probinson[2021-09-04];HPO:skoehler[2012-11-21];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001371	PMID:24566669	PCS		1/12			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001252	PMID:24566669;PMID:24348268	PCS		15/19			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001251	PMID:24566669	PCS		2/12			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001270	PMID:24348268	PCS		7/7			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0010801	PMID:24348268	PCS		5/7			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0045075	PMID:21763484	PCS		4/10			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000319	OMIM:614202	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614202	Rafiq syndrome		HP:0000718	PMID:24566669	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000316	PMID:24348268;PMID:21763484	PCS		11/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000414	PMID:24566669	PCS		7/12			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000219	PMID:24566669;PMID:24348268	PCS		13/19			P	HPO:probinson[2021-09-04];HPO:skoehler[2013-06-04];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000256	PMID:24566669	PCS		8/12			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001249	PMID:24566669;PMID:24348268	PCS		16/16			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000973	PMID:24348268	PCS		5/7			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0002553	PMID:21763484	PCS		2/10			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0005469	PMID:21763484	PCS		1/8			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000494	PMID:24348268;PMID:21763484	PCS		14/17			P	HPO:probinson[2021-09-04];HPO:skoehler[2012-11-20];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000431	OMIM:614202;PMID:21763484	PCS		12/19			P	HPO:probinson[2021-09-04];HPO:skoehler[2012-10-17]
OMIM:614202	Rafiq syndrome		HP:0000276	PMID:21763484	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001321	PMID:24348268	PCS		1/7			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001382	PMID:24566669;PMID:24348268	PCS		7/19			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001263	PMID:24566669;PMID:21763484	PCS		24/24			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000272	PMID:21763484	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000470	PMID:21763484	PCS		2/8			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0003186	PMID:24566669;PMID:24348268	PCS		9/19			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0011229	PMID:21763484	PCS		3/10			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000729	PMID:24348268	PCS		1/5			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000448	PMID:21763484	PCS		3/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000007	PMID:21763484	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000307	PMID:21763484	PCS		5/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0004209	PMID:21763484	PCS		1/7			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001956	PMID:24566669;PMID:24348268	PCS		15/19			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000268	PMID:24566669;PMID:21763484	PCS		7/20			P	HPO:probinson[2021-09-04];HPO:skoehler[2012-11-21];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000400	PMID:24348268	PCS		7/7			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000322	PMID:21763484	PCS		4/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0001513	PMID:21763484	PCS		2/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000369	PMID:24348268;PMID:21763484	PCS		8/15			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0000445	PMID:21763484	PCS		2/9			P	HPO:probinson[2021-09-04]
OMIM:614202	Rafiq syndrome		HP:0005338	PMID:24566669	PCS		7/12			P	HPO:probinson[2021-09-04]
OMIM:616415	Familial adenomatous polyposis 3		HP:0005227	PMID:25938944	PCS		7/7			P	HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0006725	PMID:25938944	PCS		1/7			P	HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0003002	PMID:25938944	PCS		1/3	FEMALE		P	HPO:skoehler[2015-06-22];HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0003003	PMID:25938944	PCS		4/7			P	HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0002671	PMID:25938944	PCS		2/7			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0003581	PMID:25938944	PCS		7/7			C	HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0002858	PMID:25938944	PCS		1/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0006771	PMID:25938944	PCS		1/7			P	HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0000007	PMID:25938944	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0012125	PMID:25938944	PCS		1/4	MALE		P	HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0012114	PMID:25938944	PCS		2/3	FEMALE		P	HPO:probinson[2022-11-08]
OMIM:616415	Familial adenomatous polyposis 3		HP:0009725	OMIM:616415	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0008209	PMID:29379881	PCS		1/1	FEMALE		P	HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001310	PMID:29379881	PCS		2/2			P	HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0003693	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001252	PMID:29379881	PCS		1/1			P	HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001251	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0002460	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0011463	PMID:29379881	PCS		1/2			C	HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0000514	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0007663	PMID:29379881	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0002359	PMID:29379881	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0007941	PMID:29379881	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001249	PMID:29379881	PCS		2/2			P	HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0006855	PMID:29379881	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001765	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001347	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0008936	PMID:29379881	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0003621	PMID:29379881	PCS		1/2			C	HPO:probinson[2022-03-10];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0003487	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0002750	PMID:29379881	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001761	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0031993	PMID:29379881	PCS		2/2			P	HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0007256	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0000007	PMID:29379881	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001510	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0001257	PMID:29379881	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-10]
OMIM:618438	Spastic ataxia 9, autosomal recessive		HP:0006886	PMID:29379881	PCS		1/2			P	HPO:probinson[2022-03-10]
OMIM:600511	Schizophrenia 3		HP:0100753	OMIM:600511	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600511	Schizophrenia 3		HP:0000707	OMIM:600511	IEA					P	HPO:iea[2009-02-17]
OMIM:600511	Schizophrenia 3		HP:0000006	OMIM:600511	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0003015	PMID:37055165	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0004325	PMID:37055165	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0007957	PMID:37055165	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0002664	PMID:37055165	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000684	PMID:37055165	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0004322	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0030353	PMID:37055165	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0003593	PMID:37055165	PCS		7/7			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0010049	PMID:37055165	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0045075	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000518	PMID:37055165	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000938	PMID:37055165	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0007663	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0002119	PMID:37055165	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000659	PMID:37055165	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0001029	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0009803	PMID:37055165	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:6000483	PMID:37055165	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000252	PMID:37055165	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000054	PMID:37055165	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000992	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0002079	PMID:37055165	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0002750	PMID:37055165	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000490	PMID:37055165	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0001263	PMID:37055165	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0034323	PMID:37055165	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0005280	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0001518	PMID:37055165	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0008066	PMID:37055165	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0034396	PMID:37055165	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000926	PMID:37055165	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0002209	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000568	PMID:37055165	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000821	PMID:37055165	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000007	PMID:37055165	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000648	PMID:37055165	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0008404	PMID:37055165	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0002007	PMID:37055165	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0001511	PMID:37055165	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000501	PMID:37055165	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620819	Rothmund-Thomson syndrome, type 4		HP:0000028	PMID:37055165	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:609253	Febrile seizures, familial, 6		HP:0002069	OMIM:609253	IEA					P	HPO:iea[2009-02-17]
OMIM:609253	Febrile seizures, familial, 6		HP:0002373	OMIM:609253	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:609253	Febrile seizures, familial, 6		HP:0011463	OMIM:609253	IEA					C	HPO:iea[2009-02-17]
OMIM:609253	Febrile seizures, familial, 6		HP:0010819	OMIM:609253	IEA					P	HPO:iea[2009-02-17]
OMIM:609253	Febrile seizures, familial, 6		HP:0010818	OMIM:609253	IEA					P	HPO:iea[2009-02-17]
OMIM:609253	Febrile seizures, familial, 6		HP:0000006	OMIM:609253	IEA					I	HPO:iea[2009-02-17]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0003581	PMID:25848748	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0032341	PMID:25848748	PCS		10/11			P	HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0003829	PMID:25848748	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0032342	PMID:25848748	PCS		9/11			P	HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0031950	PMID:25607374	PCS					P	HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0002206	PMID:25848748	PCS		15/20			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0031413	PMID:25848748	PCS					P	HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0000006	PMID:25848748	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-07]
OMIM:616373	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3		HP:0045051	PMID:25848748	PCS		7/7			P	HPO:probinson[2020-10-07]
OMIM:619040	Myofibrillar myopathy 10		HP:0003577	PMID:32779703	PCS		1/4			C	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0003621	PMID:32779703	PCS		1/4			C	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0003236	PMID:32779703	PCS		4/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0030973	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0000475	PMID:32779703	PCS		4/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0025075	PMID:32779703	PCS		1/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0003394	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0003593	PMID:32779703	PCS		1/4			C	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0410173	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0005184	PMID:32779703	PCS		1/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0012785	PMID:32779703	PCS		3/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0010548	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0006380	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0011463	PMID:32779703	PCS		1/4			C	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0002808	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0000007	PMID:32779703	PCS					I	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0001712	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0006466	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0001324	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0001852	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0002987	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0000303	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0003326	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619040	Myofibrillar myopathy 10		HP:0003458	PMID:32779703	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0003577	PMID:10712223	PCS		5/5			C	HPO:probinson[2022-03-16];HPO:probinson[2022-08-14]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0001036	OMIM:604777	TAS				HP:0012826	P	HPO:skoehler[2013-06-06]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0033252	PMID:10712223;PMID:16436457	PCS		15/15			P	HPO:probinson[2022-03-16];HPO:probinson[2022-08-14]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0001927	OMIM:604777	TAS					P	HPO:probinson[2013-03-23]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0025092	OMIM:604777	TAS				HP:0012826	P	HPO:skoehler[2017-07-13]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0000007	PMID:16436457	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2022-03-16]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0001019	OMIM:604777	TAS		HP:0040283			P	HPO:probinson[2013-03-23]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0040162	OMIM:604777	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0007479	PMID:10712223	PCS		2/5			P	HPO:probinson[2013-03-23];HPO:probinson[2022-08-14]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0040190	PMID:10712223	PCS		5/5			P	HPO:probinson[2022-08-14]
OMIM:604777	Ichthyosis, congenital, autosomal recessive 5		HP:0000982	OMIM:604777	TAS		HP:0040283			P	HPO:probinson[2013-03-23]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0000670	PMID:22341969	PCS		7/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0003577	PMID:22341969	PCS		1/8			C	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0003002	PMID:22341969	PCS	HP:0003581	1/23			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0001596	PMID:22341969	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0003593	PMID:22341969	PCS		6/8			C	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0011367	PMID:22341969	PCS		1/12			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0033832	PMID:22341969	PCS		1/12			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0012203	PMID:22341969	PCS		1/12			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0007380	PMID:22341969	PCS		12/12			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0011463	PMID:22341969	PCS		1/8			C	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0001807	PMID:22341969	PCS		4/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0011065	PMID:22341969	PCS		2/12			P	HPO:probinson[2022-10-20];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0006297	PMID:22341969	PCS		2/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0001806	PMID:22341969	PCS		1/12			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0001009	PMID:22341969	PCS		12/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0025127	PMID:22341969	PCS		1/12			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0012182	PMID:22341969	PCS	HP:0003581	10/23			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0000444	PMID:22341969	PCS		4/24			P	HPO:probinson[2022-10-20];HPO:skoehler[2014-06-24];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0008404	PMID:22341969	PCS		1/12			P	HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0000006	PMID:22341969	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:614564	Cutaneous telangiectasia and cancer syndrome, familial		HP:0005338	PMID:22341969	PCS		11/12			P	HPO:probinson[2022-10-20]
OMIM:117550	Sotos syndrome		HP:0002389	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS					P	HPO:iea[2009-02-17]
OMIM:117550	Sotos syndrome		HP:0004324	PMID:29164086	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome 1		HP:0001176	PMID:16222665;PMID:12525543	PCS		5/5			P	HPO:probinson[2022-03-14];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000486	PMID:30461603	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0001250	PMID:15942875	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0025268	PMID:30461603	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome 1		HP:0001252	PMID:12525543;PMID:28328121;PMID:29164086	PCS		4/4			P	HPO:probinson[2022-06-25];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0002020	PMID:29164086	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0045075	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000639	PMID:15942875	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0011463	PMID:30461603	PCS		1/1			C	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000718	PMID:30461603	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0011220	PMID:29164086	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0011461	PMID:29142766;PMID:28328121	PCS		3/3			C	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0010493	PMID:16222665	PCS		1/3			P	HP:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000316	PMID:16222665;PMID:28328121;PMID:29164086	PCS		3/5			P	HPO:iea[2010-10-21];HPO:probinson[2022-03-14];HPO:probinson[2022-06-25];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0006155	PMID:16222665	PCS		1/3			P	HP:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0002857	OMIM:117550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:117550	Sotos syndrome		HP:0001643	PMID:15942875	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0001763	PMID:15942875	PCS					P	HPO:iea[2010-10-25];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0001249	PMID:29142766	PCS		2/2			P	HPO:skoehler[2013-06-16];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000358	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome 1		HP:0003623	PMID:29164086	PCS		1/1			C	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0002311	OMIM:117550	TAS					P	HPO:iea[2010-10-25];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome 1		HP:0000494	PMID:30461603;PMID:12525543;PMID:28328121;PMID:29164086	PCS		4/5			P	HPO:probinson[2022-06-25];HPO:probinson[2022-03-14];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000098	PMID:16222665	PCS	HP:0003577	3/3			P	HPO:iea[2010-10-21];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001344	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0002474	OMIM:117550	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0011968	PMID:28328121;PMID:29164086	PCS		4/4			P	HPO:probinson[2022-06-25];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001382	PMID:29164086	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001263	PMID:30461603;PMID:28328121	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0009890	PMID:28328121	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0002705	OMIM:117550	TAS					P	HPO:skoehler[2015-12-30]
OMIM:117550	Sotos syndrome		HP:0001338	OMIM:117550	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0009931	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000405	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS					P	HPO:iea[2009-02-17]
OMIM:117550	Sotos syndrome		HP:0005616	PMID:16222665;PMID:29142766;PMID:29164086	PCS		5/7			P	HPO:probinson[2022-06-25];HPO:iea[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000565	PMID:30461603	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000400	PMID:16222665;PMID:30461603	PCS		4/4			P	HP:probinson[2022-03-14];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000006	PMID:11896389	PCS					I	HPO:iea[2010-10-25];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000369	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000325	PMID:29142766;PMID:28328121	PCS		2/3			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0001792	PMID:15942875	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000189	OMIM:117550	TAS					P	HPO:iea[2010-10-21];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000463	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000540	PMID:15942875	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0012801	PMID:29164086	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome 1		HP:0001270	PMID:12525543	PCS		2/2			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0002280	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS					P	HPO:iea[2009-02-17]
OMIM:117550	Sotos syndrome		HP:0001629	PMID:30461603	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0100702	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0001548	PMID:16222665	PCS		3/3			P	HP:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001548	PMID:29164086	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome 1		HP:0001548	PMID:29164086	PCS		2/2			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001548	PMID:30461603	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0001548	PMID:29142766	PCS	HP:0011461	2/2			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000337	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0002119	PMID:16222665;PMID:30461603	PCS		2/4			P	HPO:probinson[2022-06-25];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000218	PMID:12525543	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000455	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000256	PMID:12525543;PMID:29142766;PMID:28328121	PCS		4/5			P	HPO:probinson[2022-06-25];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0006579	PMID:29164086	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001347	OMIM:117550	TAS					P	HPO:iea[2009-02-17]
OMIM:117550	Sotos syndrome		HP:0000077	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS					P	HPO:iea[2010-10-25]
OMIM:117550	Sotos syndrome		HP:0000275	PMID:30461603	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome 1		HP:0000750	PMID:12525543;PMID:29164086	PCS		3/3			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0002650	PMID:15942875	PCS					P	HPO:iea[2010-10-25];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000276	PMID:16222665	PCS		2/3			P	HP:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0002572	PMID:29164086	PCS		1/1			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0005280	PMID:29142766;PMID:28328121	PCS		2/3			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0011623	PMID:30461603	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0006288	ISBN-13:978-0721606156	TAS					P	HPO:iea[2009-02-17]
OMIM:117550	Sotos syndrome		HP:0001558	PMID:28328121	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000348	PMID:30461603	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome 1		HP:0001833	PMID:16222665;PMID:12525543	PCS		5/5			P	HPO:probinson[2022-03-14];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome 1		HP:0001998	PMID:29164086	PCS		2/2			P	HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001319	PMID:29164086	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000307	PMID:12525543	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0000268	PMID:29164086	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0002007	PMID:12525543;PMID:28328121	PCS		3/3			P	HPO:probinson[2022-06-25];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001631	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS					P	HPO:iea[2009-02-17]
OMIM:117550	Sotos syndrome		HP:0007018	PMID:30461603;PMID:28328121	PCS		2/2			P	HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000388	OMIM:117550	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:117550	Sotos syndrome		HP:0000028	PMID:28328121;PMID:29164086	PCS		2/2			P	HPO:probinson[2022-06-25];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome 1		HP:0000303	PMID:16222665;PMID:12525543	PCS		4/5			P	HPO:probinson[2022-03-14];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:117550	Sotos syndrome		HP:0001952	OMIM:117550	TAS					P	HPO:iea[2010-10-21];HPO:probinson[2022-06-25]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0004467	PMID:25772936	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000384	PMID:25772936	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0003577	PMID:25772936	PCS		4/4			C	HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0001596	PMID:25772936	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000680	PMID:25772936	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000162	PMID:25772936	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0008551	PMID:25772936	PCS		3/4			P	HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0001647	PMID:25772936	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000678	PMID:25772936	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000378	PMID:25772936	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000411	PMID:25772936	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000653	PMID:25772936	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000652	PMID:25772936	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000175	PMID:25772936	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000211	OMIM:616367	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000431	OMIM:616367	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000232	PMID:25772936	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0005321	PMID:25772936	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000072	PMID:25772936	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000327	OMIM:616367	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000405	PMID:25772936	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000006	PMID:25772936	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000369	OMIM:616367	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000347	OMIM:616367	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000402	PMID:25772936	PCS		2/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-08]
OMIM:616367	Mandibulofacial dysostosis with alopecia		HP:0000324	OMIM:616367	TAS				HP:0012825	P	HPO:skoehler[2015-05-31]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0000473	PMID:24202787	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0003236	PMID:24202787	PCS					P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0003621	PMID:24202787	PCS		2/2			C	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0000750	PMID:23125284	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0003487	PMID:24202787	PCS		1/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0001266	PMID:24202787	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0002451	PMID:24202787	PCS		1/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0001260	PMID:24202787	PCS		2/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0002198	PMID:24202787	PCS					P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0002151	PMID:23125284;PMID:24202787	PCS		3/3			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0001252	PMID:23125284	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0001251	PMID:23125284;PMID:24202787	PCS		3/3			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0002490	PMID:23125284	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0003390	PMID:24202787	PCS					P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0001518	PMID:23125284	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0009027	PMID:24202787	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0000007	PMID:23125284	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0008347	PMID:23125284;PMID:24202787	PCS		11/11			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0002359	PMID:24202787	PCS	HP:0003621	1/2			P	HPO:probinson[2020-12-05]
OMIM:619054	Mitochondrial complex IV deficiency, nuclear type 11		HP:0006855	PMID:24202787	PCS		2/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:160900	Myotonic dystrophy 1		HP:0001561	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0002015	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0002059	OMIM:160900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:160900	Myotonic dystrophy 1		HP:0002486	OMIM:160900	TAS					P	HPO:probinson[2012-04-11]
OMIM:160900	Myotonic dystrophy 1		HP:0002098	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0011705	OMIM:160900	PCS					P	HPO:probinson[2012-04-11]
OMIM:160900	Myotonic dystrophy 1		HP:0001252	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0005110	PMID:15557517	PCS		1/11			P	HPO:probinson[2012-04-11]
OMIM:160900	Myotonic dystrophy 1		HP:0001262	OMIM:160900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:160900	Myotonic dystrophy 1		HP:0001081	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0002292	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0001290	OMIM:160900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:160900	Myotonic dystrophy 1		HP:0000518	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0008770	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0000029	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0001349	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0001558	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0008872	OMIM:160900	PCS					P	HPO:probinson[2012-04-11]
OMIM:160900	Myotonic dystrophy 1		HP:0004749	PMID:15557517	PCS		4/11			P	HPO:probinson[2012-04-11]
OMIM:160900	Myotonic dystrophy 1		HP:0001324	OMIM:160900	TAS					P	HPO:probinson[2012-04-11]
OMIM:160900	Myotonic dystrophy 1		HP:0000135	OMIM:160900	IEA					P	HPO:iea[2009-02-17]
OMIM:160900	Myotonic dystrophy 1		HP:0000006	OMIM:160900	IEA					I	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001771	OMIM:606612	IEA					P	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003577	PMID:11592034;OMIM:606612	PCS		14/19			C	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003236	PMID:11592034	PCS		9/9			P	HPO:probinson[2012-04-08];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0010628	OMIM:606612	PCS					P	HPO:probinson[2012-04-08]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001272	OMIM:606612	IEA					P	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003551	PMID:11592034	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001252	PMID:11592034	PCS		8/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003394	OMIM:606612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001270	PMID:11592034	PCS		5/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0030319	PMID:11592034	PCS		1/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003307	OMIM:606612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002878	PMID:11592034	PCS		1/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002119	OMIM:606612	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0007126	PMID:11592034	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002359	OMIM:606612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0000158	OMIM:606612	IEA		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001324	PMID:11592034	PCS		3/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001302	OMIM:606612	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003701	OMIM:606612	TAS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003547	PMID:11592034	PCS		11/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003724	PMID:11592034	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001249	OMIM:606612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003326	OMIM:606612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003623	PMID:11592034	PCS		5/9			C	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003202	PMID:11592034	PCS		1/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002015	PMID:11592034	PCS		1/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003324	PMID:11592034	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0000252	OMIM:606612	IEA					P	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002650	PMID:11592034	PCS		1/9			P	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001288	PMID:11592034	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0011968	PMID:11592034	PCS		4/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002350	OMIM:606612	IEA					P	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003560	OMIM:606612	PCS					P	HPO:probinson[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002194	OMIM:606612	PCS					P	HPO:probinson[2012-04-08]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002091	OMIM:606612	IEA		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002808	OMIM:606612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0008981	OMIM:606612	IEA		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002948	OMIM:606612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0000007	PMID:11592034	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0001319	OMIM:606612	IEA					P	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0030051	OMIM:606612	TAS					P	HPO:skoehler[2014-11-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0002500	OMIM:606612	IEA					P	HPO:iea[2009-02-17]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0034391	PMID:11592034	PCS		1/9			P	HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003458	PMID:11592034	PCS					P	HPO:probinson[2012-04-08];HPO:probinson[2023-02-27]
OMIM:606612	Muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5		HP:0003733	OMIM:606612	IEA					P	HPO:iea[2009-02-17]
OMIM:600263	Helicobacter pylori infection, susceptibility to		HP:0005202	OMIM:600263	IEA					P	HPO:iea[2009-02-17]
DECIPHER:74	15q13.3 microdeletion syndrome		HP:0000271	DECIPHER:74	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:74	15q13.3 microdeletion syndrome		HP:0001250	DECIPHER:74	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:74	15q13.3 microdeletion syndrome		HP:0001249	DECIPHER:74	IEA					P	HPO:skoehler[2013-05-29]
OMIM:226735	Epidermolysis bullosa with diaphragmatic hernia		HP:0008066	OMIM:226735	IEA					P	HPO:skoehler[2009-02-17]
OMIM:226735	Epidermolysis bullosa with diaphragmatic hernia		HP:0000007	OMIM:226735	IEA					I	HPO:iea[2009-02-17]
OMIM:226735	Epidermolysis bullosa with diaphragmatic hernia		HP:0003811	OMIM:226735	IEA					C	HPO:iea[2009-02-17]
OMIM:226735	Epidermolysis bullosa with diaphragmatic hernia		HP:0007446	OMIM:226735	IEA					P	HPO:skoehler[2009-02-17]
OMIM:226735	Epidermolysis bullosa with diaphragmatic hernia		HP:0000776	OMIM:226735	IEA					P	HPO:skoehler[2009-02-17]
OMIM:615108	Cowden syndrome 5		HP:0000365	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000221	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0001250	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000160	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0010609	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0001031	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0004481	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0002080	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000518	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000836	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0100646	OMIM:615108	TAS					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0002858	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000854	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000218	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0001626	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000972	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000138	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000853	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0001249	OMIM:615108	TAS		12%			P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0001102	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0002650	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0003002	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000034	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000771	OMIM:615108	TAS			MALE		P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0002253	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0003581	OMIM:615108	TAS					C	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0004390	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0002808	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000327	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000767	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000821	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0006740	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000006	PMID:23246288	PCS					I	HPO:skoehler[2015-09-25];HPO:probinson[2021-05-02]
OMIM:615108	Cowden syndrome 5		HP:0000347	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:615108	Cowden syndrome 5		HP:0000545	OMIM:615108	IEA					P	HPO:skoehler[2015-09-25]
OMIM:614389	Pregnancy loss, recurrent, susceptibility to, 1		HP:0011462	OMIM:614389	TAS					C	HPO:probinson[2022-10-01]
OMIM:614389	Pregnancy loss, recurrent, susceptibility to, 1		HP:0200067	OMIM:614389	TAS					H	HPO:skoehler[2013-05-31]
OMIM:614389	Pregnancy loss, recurrent, susceptibility to, 1		HP:0000006	OMIM:614389	TAS					I	HPO:skoehler[2012-10-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0002212	OMIM:258360	IEA					P	HPO:iea[2009-02-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0007717	OMIM:258360	IEA					P	HPO:iea[2009-02-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0001263	OMIM:258360	IEA					P	HPO:skoehler[2019-09-07]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0410252	OMIM:258360	IEA					P	HPO:skoehler[2019-02-22]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0010764	OMIM:258360	TAS					P	HPO:probinson[2015-07-18]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0002719	OMIM:258360	IEA					P	HPO:iea[2009-02-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0001804	OMIM:258360	IEA					P	HPO:iea[2009-02-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0000007	OMIM:258360	IEA					I	HPO:iea[2009-02-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0009886	OMIM:258360	TAS					P	HPO:probinson[2012-07-22]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0100827	OMIM:258360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0007665	OMIM:258360	TAS					P	HPO:probinson[2015-07-18]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0001598	OMIM:258360	IEA					P	HPO:iea[2009-02-17]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0002225	OMIM:258360	IEA					P	HPO:skoehler[2010-06-18]
OMIM:258360	Onychotrichodysplasia and neutropenia		HP:0001875	OMIM:258360	TAS					P	HPO:probinson[2009-02-17]
OMIM:608978	Meacham syndrome		HP:0003577	PMID:17853480	PCS					C	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0002089	PMID:17853480	PCS		10/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001651	PMID:17853480	PCS		2/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001195	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001153	PMID:17853480	PCS		6/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0000085	PMID:17853480	PCS		1/8			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0004383	PMID:17853480	PCS		5/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0040314	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001629	PMID:17853480	PCS		3/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0033210	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001669	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001647	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0003826	PMID:17853480	PCS		1/13			C	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0000813	PMID:17853480	PCS		2/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001747	PMID:17853480	PCS		2/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0000037	PMID:17853480	PCS		13/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001643	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001522	PMID:17853480	PCS		3/13			C	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0005301	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001680	PMID:17853480	PCS		2/13			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0010773	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0011565	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0011626	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0011720	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0032592	PMID:17853480	PCS		4/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0003819	PMID:17853480	PCS		1/13			C	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0009110	PMID:17853480	PCS		2/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0012020	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0009112	PMID:17853480	PCS		7/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001636	PMID:17853480	PCS		1/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0003811	PMID:17853480	PCS		8/13			C	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0001631	PMID:17853480	PCS		3/13			P	HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0000006	PMID:17853480	PCS					I	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:608978	Meacham syndrome		HP:0000105	PMID:17853480	PCS		2/8			P	HPO:probinson[2021-08-19]
OMIM:301201	Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2		HP:0000705	OMIM:301201	IEA					P	HPO:skoehler[2010-06-18]
OMIM:301201	Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2		HP:0001417	OMIM:301201	IEA					I	HPO:iea[2009-02-17]
OMIM:611597	Cataract, autosomal dominant, multiple types 1		HP:0000519	PMID:10739768	PCS					P	HPO:probinson[2009-02-17]
OMIM:611597	Cataract, autosomal dominant, multiple types 1		HP:0000006	OMIM:611597	TAS					I	HPO:probinson[2009-02-17]
OMIM:611597	Cataract, autosomal dominant, multiple types 1		HP:0000545	OMIM:611597	TAS					P	HPO:probinson[2009-02-17]
OMIM:611597	Cataract, autosomal dominant, multiple types 1		HP:0007834	OMIM:611597	TAS					P	HPO:probinson[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0004322	PMID:31438591	PCS		29/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001772	OMIM:130070	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001371	PMID:31438591	PCS		4/9			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000160	PMID:31438591	PCS		28/30			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001252	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001373	PMID:31438591	PCS					P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001290	PMID:31438591	PCS		10/32			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0011342	PMID:31438591	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0002816	OMIM:130070	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000316	PMID:31438591	PCS		28/32			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000954	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001763	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0002974	PMID:31438591	PCS		18/31			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000175	PMID:31438591	PCS		4/31			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0002673	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001382	PMID:31438591	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0010511	OMIM:130070	TAS					P	HPO:skoehler[2013-08-10]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0011800	PMID:31438591	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0003083	PMID:31438591	PCS		17/31			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000007	PMID:31438591	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000768	OMIM:130070	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0005616	PMID:31438591	PCS		1/32			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000520	PMID:31438591	PCS		28/30			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000369	PMID:31438591	PCS		7/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0003015	PMID:31438591	PCS		4/8			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000387	OMIM:130070	TAS					P	HPO:probinson[2015-02-02]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000540	PMID:31438591	PCS		12/29			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001075	PMID:31438591	PCS		4/32			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001270	PMID:31438591	PCS		10/32			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0012368	PMID:31438591	PCS		29/32			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001508	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000938	PMID:31438591	PCS		6/32			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000337	PMID:31438591	PCS		29/32			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0002757	PMID:31438591	PCS		1/10			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000774	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000256	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0007469	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000894	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000974	PMID:31438591	PCS		30/32			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001166	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000274	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001363	PMID:31438591	PCS	HP:0003577	6/8			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0002650	PMID:31438591	PCS		7/32			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0001762	OMIM:130070	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000431	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0011308	OMIM:130070	TAS					P	HPO:skoehler[2013-08-10]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000193	PMID:31438591	PCS		4/31			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000592	PMID:31438591	PCS		6/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0006243	OMIM:130070	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0002209	OMIM:130070	IEA					P	HPO:iea[2009-02-17]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0006487	OMIM:130070	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0000347	PMID:31438591	PCS		3/32			P	HPO:probinson[2020-08-08]
OMIM:130070	Ehlers-Danlos syndrome, spondylodysplastic type, 1		HP:0004425	OMIM:130070	IEA					P	HPO:skoehler[2018-10-08]
OMIM:122460	Coronavirus 229E susceptibility		HP:0005396	OMIM:122460	IEA					P	HPO:iea[2009-02-17]
OMIM:122460	Coronavirus 229E susceptibility		HP:0000006	OMIM:122460	IEA					I	HPO:iea[2009-02-17]
OMIM:617694	Al Kaissi syndrome		HP:0004325	PMID:28886341	PCS		4/9			P	HPO:probinson[2018-05-23];HPO:probinson[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0000286	PMID:28886341	PCS		9/9		HP:0012832	P	HPO:probinson[2018-05-23];HPO:probinson[2021-09-02]
OMIM:617694	Al Kaissi syndrome		HP:0001572	PMID:28886341	PCS		2/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000486	PMID:28886341	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0004322	PMID:28886341	PCS		8/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0001250	PMID:28886341	PCS		2/9			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0430046	PMID:28886341	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0025300	PMID:28886341	PCS		3/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0001290	OMIM:617694	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617694	Al Kaissi syndrome		HP:0033725	PMID:28886341	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0006191	PMID:28886341	PCS		4/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0010055	PMID:28886341	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0000319	PMID:28886341	PCS		4/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0002937	OMIM:617694	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0000316	OMIM:617694	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0008897	PMID:28886341	PCS		8/9			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0000752	PMID:28886341	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0001763	PMID:28886341	PCS		3/9			P	HPO:skoehler[2019-04-18]
OMIM:617694	Al Kaissi syndrome		HP:0001249	PMID:28886341	PCS		9/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000358	PMID:28886341	PCS		9/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000494	PMID:28886341	PCS		4/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000252	PMID:28886341	PCS		6/9			P	HPO:skoehler[2019-04-18]
OMIM:617694	Al Kaissi syndrome		HP:0002079	OMIM:617694	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0000331	PMID:28886341	PCS		5/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0001382	PMID:28886341	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0001263	PMID:28886341	PCS		9/9			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0040195	PMID:28886341	PCS					P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000007	PMID:28886341	PCS					I	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0002705	PMID:28886341	PCS		4/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0007598	PMID:28886341	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0000960	PMID:28886341	PCS		5/9			P	HPO:skoehler[2019-04-18]
OMIM:617694	Al Kaissi syndrome		HP:0000248	PMID:28886341	PCS		1/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000369	PMID:28886341	PCS		9/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000325	PMID:28886341	PCS		4/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0003577	PMID:28886341	PCS		9/9			C	HPO:skoehler[2019-04-18]
OMIM:617694	Al Kaissi syndrome		HP:0000343	PMID:28886341	PCS		9/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000219	OMIM:617694	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0002119	PMID:28886341	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0030084	PMID:28886341	PCS		1/9			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0000218	PMID:28886341	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0000455	PMID:28886341	PCS		9/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000377	OMIM:617694	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0000473	PMID:28886341	PCS		2/9			P	HPO:skoehler[2019-04-18]
OMIM:617694	Al Kaissi syndrome		HP:0002136	PMID:28886341	PCS		2/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0000750	PMID:28886341	PCS		9/9			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0000431	PMID:28886341	IEA		3/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0031936	PMID:28886341	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0000272	PMID:28886341	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:617694	Al Kaissi syndrome		HP:0005280	PMID:28886341	PCS		6/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000506	PMID:28886341	PCS		7/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000307	PMID:28886341	PCS		2/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0001511	PMID:28886341	PCS		5/9			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0007413	PMID:28886341	PCS		3/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0200055	PMID:28886341	PCS		8/9			P	HPO:probinson[2018-05-23]
OMIM:617694	Al Kaissi syndrome		HP:0000664	PMID:28886341	PCS		1/9			P	HPO:skoehler[2018-10-08]
OMIM:617694	Al Kaissi syndrome		HP:0001631	PMID:28886341;OMIM:617694	PCS		2/19			P	HPO:skoehler[2019-04-18];ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0000252	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0001344	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0002540	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0000365	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0001263	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0001252	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0000718	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0000007	PMID:32129449	PCS					I	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0001270	PMID:32129449	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620038	Neurodevelopmental disorder with microcephaly, hypotonia, and absent language		HP:0007018	PMID:32129449	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:607487	Cardiomyopathy, familial hypertrophic, 25		HP:0001716	PMID:15582318	PCS		1/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-07-11]
OMIM:607487	Cardiomyopathy, familial hypertrophic, 25		HP:0001639	PMID:15582318	PCS		2/2			P	HPO:probinson[2022-07-11]
OMIM:607487	Cardiomyopathy, familial hypertrophic, 25		HP:0003581	PMID:15582318	PCS		2/2			C	HPO:probinson[2022-07-11]
OMIM:607487	Cardiomyopathy, familial hypertrophic, 25		HP:0001712	PMID:15582318	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-07-11]
OMIM:607487	Cardiomyopathy, familial hypertrophic, 25		HP:0000006	PMID:15582318	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-07-11]
OMIM:209885	Barber-Say syndrome		HP:0000365	PMID:26119818	PCS		1/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000684	PMID:26119818	PCS		1/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0010648	PMID:26119818	PCS		2/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0045075	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0011266	PMID:26119818	PCS		8/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000958	PMID:26119818	PCS		3/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000998	PMID:26119818	PCS		12/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000316	PMID:26119818	PCS		4/12			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0001249	PMID:26119818	PCS		1/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0004334	PMID:26119818	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0001582	PMID:26119818	PCS		8/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000294	PMID:26119818	PCS		4/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0011298	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000327	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000689	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0004209	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000402	PMID:26119818	PCS		6/12			P	HPO:probinson[2022-05-07];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000369	PMID:26119818	PCS		2/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000006	PMID:26119818	PCS					I	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000445	PMID:26119818	PCS		8/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000687	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000220	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0003577	PMID:26119818	PCS		12/12			C	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0001156	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000463	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0002561	PMID:26119818	PCS		1/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000064	PMID:26119818	PCS		1/9			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0009125	PMID:26119818	PCS		2/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000656	PMID:26119818	PCS		11/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000414	PMID:26119818	PCS		12/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000218	PMID:26119818	PCS		1/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000653	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0002557	PMID:26119818	PCS		9/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000059	PMID:26119818	PCS		1/9			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000212	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000154	PMID:26119818	PCS		12/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000233	PMID:26119818	PCS		2/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0001762	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000750	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000430	PMID:26119818	PCS		1/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0003186	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0011225	PMID:26119818	PCS		2/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0400002	PMID:26119818	PCS		2/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0100678	PMID:26119818	PCS		4/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000506	PMID:26119818	PCS		3/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000668	PMID:26119818	PCS		1/12			P	HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000347	PMID:26119818	PCS		2/12			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-05-07]
OMIM:209885	Barber-Say syndrome		HP:0000303	OMIM:209885	TAS					P	HPO:skoehler[2012-10-12]
OMIM:209885	Barber-Say syndrome		HP:0000028	PMID:26119818	PCS		1/3			P	HPO:probinson[2022-05-07]
OMIM:615083	Colorectal cancer, susceptibility to, 12		HP:0030731	OMIM:615083	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615083	Colorectal cancer, susceptibility to, 12		HP:0003581	OMIM:615083	TAS					C	HPO:skoehler[2013-02-25]
OMIM:615083	Colorectal cancer, susceptibility to, 12		HP:0000006	OMIM:615083	TAS					I	HPO:skoehler[2013-02-25]
OMIM:615083	Colorectal cancer, susceptibility to, 12		HP:0200063	OMIM:615083	TAS					P	HPO:skoehler[2013-05-31]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001276	PMID:29220673	PCS	HP:0003623	2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0002267	PMID:29220673	PCS		2/5			P	HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0002540	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000486	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0004322	PMID:29220673	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0002120	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001250	PMID:29220673	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0003593	PMID:29220673	PCS		5/5			C	HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0010845	PMID:29220673	PCS		1/5			P	HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001508	PMID:29220673	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000639	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000737	PMID:29220673	PCS	HP:0003623	2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000736	PMID:29220673	PCS		2/5			P	HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001249	PMID:29220673	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000252	PMID:29220673	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0002510	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001344	PMID:29220673	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0002133	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0031936	PMID:29220673	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0002079	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0011968	PMID:29220673	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001263	PMID:29220673	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0002072	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0011800	PMID:29220673	PCS		1/5			P	HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000609	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0034392	PMID:29220673	PCS		1/5			P	HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001319	PMID:29220673	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000400	PMID:29220673	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0001257	PMID:29220673	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000322	PMID:29220673	PCS		1/5			P	HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000006	PMID:29220673	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617864	Neurodevelopmental disorder with or without seizures and gait abnormalities		HP:0000303	PMID:29220673	PCS		1/5			P	HPO:probinson[2023-02-06]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0002224	PMID:33909043	PCS		2/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000343	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0002188	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0003593	PMID:33909043	PCS		2/2			C	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0045075	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0008070	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0012179	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0020045	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000219	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0009886	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000411	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000278	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0002599	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000973	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0001264	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0003487	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0001263	PMID:33909043	PCS		2/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0001284	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0011448	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0100876	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0008003	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000448	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000007	PMID:33909043	PCS					I	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000964	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0000601	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:619691	Trichothiodystrophy 8, nonphotosensitive		HP:0001257	PMID:33909043	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0031956	PMID:31479177	PCS		2/3			P	HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0001396	PMID:31479177	PCS		3/3			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0004322	PMID:31479177	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0003593	PMID:31479177	PCS		3/3			C	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0002240	PMID:31479177	PCS		2/3			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0000093	PMID:31479177	PCS		3/3			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0012202	PMID:31479177	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0031964	PMID:31479177	PCS		2/3			P	HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0002908	PMID:31479177	PCS		3/3			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0002904	PMID:31479177	PCS		3/3			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0000007	PMID:31479177	PCS					I	HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0000989	PMID:31479177	PCS		3/3			P	HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0001744	PMID:31479177	PCS		2/3			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0000952	PMID:31479177	PCS		2/3			P	HPO:probinson[2022-08-27]
OMIM:620010	Cholestasis, progressive familial intrahepatic, 12		HP:0003645	PMID:31479177	PCS		2/3			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:300645	Atypical mycobacteriosis, familial, X-linked 2		HP:0032262	PMID:21278736	PCS		1/7			P	HPO:probinson[2023-01-18];HPO:probinson[2023-01-18]
OMIM:300645	Atypical mycobacteriosis, familial, X-linked 2		HP:0001419	PMID:21278736	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-18]
OMIM:300645	Atypical mycobacteriosis, familial, X-linked 2		HP:0011274	PMID:21278736	PCS					P	HPO:skoehler[2012-10-19];HPO:probinson[2023-01-18]
OMIM:300645	Atypical mycobacteriosis, familial, X-linked 2		HP:0020087	PMID:21278736	PCS		6/7			P	HPO:probinson[2023-01-18]
OMIM:300645	Atypical mycobacteriosis, familial, X-linked 2		HP:0003593	PMID:21278736	PCS		7/7			C	HPO:probinson[2023-01-18]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0002014	PMID:32737136	PCS		2/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0003577	PMID:32737136	PCS		1/9			C	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0003593	PMID:32737136	PCS		4/9			C	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0002240	PMID:32737136	PCS		9/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0034328	PMID:32737136	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0001409	PMID:32737136	PCS		4/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0011463	PMID:32737136	PCS		4/9			C	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0000007	PMID:32737136	PCS					I	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0006563	PMID:32737136	PCS		7/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0000989	PMID:32737136	PCS		1/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0001945	PMID:32737136	PCS		2/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0001406	PMID:32737136	PCS		2/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0000952	PMID:32737136	PCS		3/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0001744	PMID:32737136	PCS		7/9			P	HPO:probinson[2022-06-05]
OMIM:619849	Cholestasis, progressive familial intrahepatic, 9		HP:0001413	PMID:32737136	PCS		1/9			P	HPO:probinson[2022-06-05]
OMIM:219300	Cutis verticis gyrata and mental deficiency		HP:0000007	OMIM:219300	IEA					I	HPO:iea[2009-02-17]
OMIM:219300	Cutis verticis gyrata and mental deficiency		HP:0010541	OMIM:219300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219300	Cutis verticis gyrata and mental deficiency		HP:0001249	OMIM:219300	IEA					P	HPO:iea[2009-02-17]
OMIM:175510	Gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial		HP:0002576	OMIM:175510	TAS					P	HPO:probinson[2009-02-17]
OMIM:175510	Gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial		HP:0200008	OMIM:175510	TAS					P	HPO:iea[2009-02-17]
OMIM:175510	Gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial		HP:0100723	PMID:25975287	PCS					P	HPO:probinson[2020-07-21]
OMIM:175510	Gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial		HP:0000006	PMID:25975287	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2020-07-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001892	PMID:30247636;PMID:36395340	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0002021	PMID:33510604;PMID:30247636	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0003493	PMID:30247636	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0002240	PMID:34159722;PMID:36395340	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0040185	PMID:34159722;PMID:30247636;PMID:36395340	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0031689	PMID:33510604;PMID:34159722;PMID:30247636;PMID:36395340	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0000518	PMID:34159722;PMID:36395340	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001903	PMID:33510604;PMID:34159722;PMID:30247636;PMID:36395340	PCS		7/10			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0011463	PMID:30247636	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001888	PMID:34159722;PMID:30247636	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001902	PMID:30247636;PMID:36395340	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001704	PMID:33510604;PMID:30247636;PMID:36395340	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001923	PMID:30247636	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0005528	PMID:30247636	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:4000208	PMID:34159722	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001249	PMID:34159722;PMID:36395340	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0003623	PMID:33510604;PMID:34159722;PMID:30247636;PMID:36395340	PCS		9/10			C	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001342	PMID:30247636	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001882	PMID:33510604;PMID:34159722;PMID:30247636;PMID:36395340	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0012024	PMID:34159722	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0031385	PMID:33510604;PMID:30247636	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0000007	PMID:30247636	PCS					I	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001873	PMID:33510604;PMID:30247636	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0000421	PMID:34159722;PMID:36395340	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001876	PMID:33510604;PMID:30247636	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001634	PMID:33510604;PMID:30247636;PMID:36395340	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0001875	PMID:33510604;PMID:30247636;PMID:36395340	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:620776	Thrombocytopenia 13, syndromic		HP:0000225	PMID:34159722	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:300123	Intellectual developmental disorder, X-linked, with isolated growth hormone deficiency		HP:0000871	OMIM:300123	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300123	Intellectual developmental disorder, X-linked, with isolated growth hormone deficiency		HP:0004322	OMIM:300123	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300123	Intellectual developmental disorder, X-linked, with isolated growth hormone deficiency		HP:0001263	OMIM:300123	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300123	Intellectual developmental disorder, X-linked, with isolated growth hormone deficiency		HP:0000821	OMIM:300123	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300123	Intellectual developmental disorder, X-linked, with isolated growth hormone deficiency		HP:0000824	OMIM:300123	IEA					P	HPO:skoehler[2015-01-21]
OMIM:300123	Intellectual developmental disorder, X-linked, with isolated growth hormone deficiency		HP:0001417	PMID:17400794	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-24]
OMIM:254200	Myasthenia gravis		HP:0002960	OMIM:254200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:254200	Myasthenia gravis		HP:0005216	OMIM:254200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:254200	Myasthenia gravis		HP:0002015	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0010628	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0000651	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0003473	OMIM:254200	TAS					P	HPO:skoehler[2015-01-21]
OMIM:254200	Myasthenia gravis		HP:0001260	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0003690	OMIM:254200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254200	Myasthenia gravis		HP:0000818	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0100522	OMIM:254200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:254200	Myasthenia gravis		HP:0000508	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0002715	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0001426	OMIM:254200	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:254200	Myasthenia gravis		HP:0003701	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:254200	Myasthenia gravis		HP:0001611	OMIM:254200	IEA					P	HPO:iea[2009-02-17]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0001051	PMID:23509104	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0034049	PMID:24838973	PCS		3/3	MALE		P	HPO:probinson[2022-02-05]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0030839	PMID:23509104	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0001072	PMID:23509104	PCS		2/2			P	HPO:probinson[2015-03-22];HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0001061	PMID:23509104	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0010541	OMIM:167100	TAS					P	HPO:skoehler[2010-06-20]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0100759	PMID:23509104	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0100759	PMID:24838973	PCS		3/3	MALE		P	HPO:probinson[2021-10-16]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0100759	PMID:24838973	PCS		0/3	FEMALE		P	HPO:probinson[2021-10-16]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0011462	PMID:23509104	PCS		2/2			C	HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0000508	OMIM:167100	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0000975	PMID:23509104	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0006465	PMID:23509104	PCS		2/2			P	HPO:probinson[2015-03-22];HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0005208	PMID:23509104	PCS		1/2			P	HPO:probinson[2021-07-10]
OMIM:167100	Hypertrophic osteoarthropathy, primary, autosomal dominant		HP:0000006	OMIM:167100	TAS					I	HPO:probinson[2009-02-17]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0003621	PMID:38272031	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0003596	PMID:38272031	PCS		3/8			C	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0025159	PMID:38272031	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0011462	PMID:38272031	PCS		4/8			C	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0007663	PMID:38272031	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0000007	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0007401	PMID:38272031	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0000603	PMID:38272031	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0007754	PMID:38272031	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0012511	PMID:38272031	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620762	Macular dystrophy with or without cone dysfunction		HP:0007722	PMID:38272031	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0002135	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0000572	OMIM:259730	TAS					P	HPO:skoehler[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0003148	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0004322	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0003034	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0007807	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0008341	PMID:8834238	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0011002	PMID:8834238	PCS		2/2			P	HPO:skoehler[2015-01-21]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0001903	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0008153	OMIM:259730	TAS					P	HPO:skoehler[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0000007	PMID:8834238	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0000689	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0000505	OMIM:259730	IEA					P	HPO:skoehler[2018-10-08]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0001978	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0001433	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0002514	PMID:8834238	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0004437	OMIM:259730	IEA					P	HPO:iea[2009-02-17]
OMIM:259730	Osteopetrosis, autosomal recessive 3		HP:0001249	PMID:8834238	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-27]
OMIM:211990	Camptomelic syndrome, Long-Limb type		HP:0002983	OMIM:211990	TAS				HP:0012825	P	HPO:probinson[2012-07-26]
OMIM:211990	Camptomelic syndrome, Long-Limb type		HP:0000007	OMIM:211990	TAS					I	HPO:probinson[2009-02-17]
OMIM:211990	Camptomelic syndrome, Long-Limb type		HP:0006487	OMIM:211990	TAS					P	HPO:probinson[2012-07-26]
OMIM:163400	Nievergelt syndrome		HP:0003048	OMIM:163400	IEA					P	HPO:iea[2009-02-17]
OMIM:163400	Nievergelt syndrome		HP:0003577	PMID:17702012	PCS		2/2			C	HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0003027	OMIM:163400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:163400	Nievergelt syndrome		HP:0001440	OMIM:163400	IEA					P	HPO:iea[2009-02-17]
OMIM:163400	Nievergelt syndrome		HP:0001762	OMIM:163400	IEA					P	HPO:iea[2009-02-17]
OMIM:163400	Nievergelt syndrome		HP:0001761	PMID:17702012	PCS		2/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0004322	PMID:17702012	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0000271	PMID:17702012	PCS		0/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0010781	OMIM:163400	IEA					P	HPO:skoehler[2009-02-17]
OMIM:163400	Nievergelt syndrome		HP:0002857	PMID:17702012	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0008368	OMIM:163400	IEA					P	HPO:iea[2009-02-17]
OMIM:163400	Nievergelt syndrome		HP:0001840	PMID:17702012	PCS		2/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0000006	PMID:17702012	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0001249	PMID:17702012	PCS		0/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-08]
OMIM:163400	Nievergelt syndrome		HP:0008845	OMIM:163400	IEA					P	HPO:iea[2009-02-17]
OMIM:163400	Nievergelt syndrome		HP:0002974	OMIM:163400	IEA					P	HPO:iea[2009-02-17]
OMIM:612908	Keratosis palmoplantaris striata II		HP:0001595	PMID:9887343	PCS		0/26			P	HPO:probinson[2013-04-07];HPO:probinson[2022-12-12];HPO:probinson[2024-03-14]
OMIM:612908	Keratosis palmoplantaris striata II		HP:0000164	PMID:9887343	PCS		0/26			P	HPO:probinson[2013-04-07];HPO:probinson[2022-12-12];HPO:probinson[2024-03-14]
OMIM:612908	Keratosis palmoplantaris striata II		HP:0003621	PMID:9887343	PCS					C	HPO:probinson[2022-12-12]
OMIM:612908	Keratosis palmoplantaris striata II		HP:0001597	PMID:9887343	PCS		0/26			P	HPO:probinson[2013-04-07];HPO:probinson[2022-12-12];HPO:probinson[2024-03-14]
OMIM:612908	Keratosis palmoplantaris striata II		HP:0025092	PMID:9887343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-12]
OMIM:612908	Keratosis palmoplantaris striata II		HP:0000982	PMID:9887343	PCS		26/26			P	HPO:probinson[2013-04-07];HPO:probinson[2022-12-12];HPO:probinson[2024-03-14]
OMIM:612908	Keratosis palmoplantaris striata II		HP:0000006	PMID:9887343	PCS					I	HPO:probinson[2013-04-07];HPO:probinson[2022-12-12]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0002179	PMID:34037727	PCS		2/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0002421	PMID:34037727	PCS		2/2			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0031956	PMID:34037727	PCS		2/2			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0002079	PMID:34037727	PCS		2/2			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0001272	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0011968	PMID:34037727	PCS	HP:0003623	2/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0010818	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0005484	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0011344	PMID:34037727	PCS		2/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0011003	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0012202	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0031964	PMID:34037727	PCS		2/2			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0012595	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0003819	PMID:34037727	PCS		1/2			C	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0000737	PMID:34037727	PCS		2/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0002904	PMID:34037727	PCS	HP:0003623	2/2			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0040288	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0000007	PMID:34037727	PCS					I	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0020045	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0001406	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0008689	PMID:34037727	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:619685	Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis		HP:0003623	PMID:34037727	PCS		2/2			C	HPO:probinson[2022-03-27]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0003236	PMID:22703880	PCS		0/6			P	HPO:skoehler[2013-03-11];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0010628	PMID:22703880	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0003676	PMID:22703880	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002123	PMID:22703880	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0003391	OMIM:159950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0011463	PMID:22703880	PCS		1/6			C	HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0001308	PMID:22703880	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0007269	PMID:22703880	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002359	PMID:22703880	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0003701	PMID:22703880	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0008955	OMIM:159950	IEA					P	HPO:iea[2009-02-17]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0003202	PMID:22703880	PCS		6/6			P	HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0003621	PMID:22703880	PCS		5/6			C	HPO:probinson[2013-03-11];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002015	PMID:22703880	PCS		1/6			P	HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002650	PMID:22703880	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002398	OMIM:159950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0001288	PMID:22703880	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002197	PMID:22703880	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0001284	PMID:22703880	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0000726	OMIM:159950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0000007	PMID:22703880	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002747	OMIM:159950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0002205	PMID:22703880	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0001337	PMID:22703880	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:159950	Spinal muscular atrophy with progressive myoclonic epilepsy		HP:0001336	PMID:22703880	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0002353	PMID:27567911	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0000750	PMID:27567911	PCS		2/2			P	HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0001272	PMID:27567911	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0001263	PMID:27567911	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0003593	PMID:27567911	PCS		2/2			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0001290	PMID:27567911	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0032794	PMID:27567911	PCS		2/2			P	HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0000007	PMID:27567911	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:617643	Cerebellar atrophy, developmental delay, and seizures		HP:0007334	PMID:27567911	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:606996	Senior-Loken syndrome 4		HP:0003774	OMIM:606996	IEA	HP:0011462	21/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606996	Senior-Loken syndrome 4		HP:0001583	OMIM:606996	IEA					P	HPO:iea[2009-02-17]
OMIM:606996	Senior-Loken syndrome 4		HP:0001959	OMIM:606996	IEA					P	HPO:iea[2009-02-17]
OMIM:606996	Senior-Loken syndrome 4		HP:0001903	OMIM:606996	IEA					P	HPO:iea[2009-02-17]
OMIM:606996	Senior-Loken syndrome 4		HP:0001141	OMIM:606996	IEA					P	HPO:iea[2009-02-17]
OMIM:606996	Senior-Loken syndrome 4		HP:0000646	OMIM:606996	IEA					P	HPO:iea[2009-02-17]
OMIM:606996	Senior-Loken syndrome 4		HP:0000007	PMID:12205563	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606996	Senior-Loken syndrome 4		HP:0000090	OMIM:606996	IEA					P	HPO:iea[2009-02-17]
OMIM:606996	Senior-Loken syndrome 4		HP:0000103	OMIM:606996	IEA					P	HPO:iea[2009-02-17]
OMIM:606996	Senior-Loken syndrome 4		HP:0000510	PMID:12205563	PCS		7/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0002224	PMID:12373648	PCS		0/11			P	HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0001663	PMID:12373648	PCS		2/11			P	HPO:probinson[2012-07-16];HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0025708	PMID:12373648	PCS		1/1			C	HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0006682	PMID:12373648	PCS		5/11			P	HPO:probinson[2012-07-16];HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0001635	PMID:12373648	PCS	HP:0003584	1/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0011663	PMID:12373648	PCS		11/11			P	HPO:probinson[2012-07-16];HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0000006	PMID:12373648	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0001645	PMID:12373648	PCS		2/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-10]
OMIM:607450	Arrhythmogenic right ventricular dysplasia, familial, 8		HP:0004756	PMID:12373648	PCS		2/11			P	HPO:probinson[2012-07-16];HPO:probinson[2022-07-10]
OMIM:176780	Pelvic organ prolapse		HP:0002035	OMIM:176780	IEA					P	HPO:iea[2009-02-17]
OMIM:176780	Pelvic organ prolapse		HP:0002607	OMIM:176780	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176780	Pelvic organ prolapse		HP:0000006	OMIM:176780	IEA					I	HPO:iea[2009-02-17]
OMIM:121800	Corneal dystrophy, crystalline, of schnyder		HP:0001131	OMIM:121800	IEA					P	HPO:skoehler[2015-01-19]
OMIM:121800	Corneal dystrophy, crystalline, of schnyder		HP:0007760	OMIM:121800	IEA					P	HPO:iea[2009-02-17]
OMIM:121800	Corneal dystrophy, crystalline, of schnyder		HP:0000006	OMIM:121800	IEA					I	HPO:iea[2009-02-17]
OMIM:619108	Spermatogenic failure 48		HP:0003251	PMID:32017041	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619108	Spermatogenic failure 48		HP:0003581	PMID:32673564	IEA					C	HPO:probinson[2020-12-08]
OMIM:619108	Spermatogenic failure 48		HP:0000007	PMID:32017041	PCS					I	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619108	Spermatogenic failure 48		HP:0031038	PMID:32673564	PCS					P	HPO:probinson[2020-12-08]
OMIM:619108	Spermatogenic failure 48		HP:0000798	PMID:32017041	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619108	Spermatogenic failure 48		HP:0000027	PMID:32673564	PCS		10/10			P	HPO:probinson[2020-12-08]
OMIM:611554	Leopard syndrome 2		HP:0000286	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0002212	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000494	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0001003	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0004322	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000470	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0005280	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000958	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0001639	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000957	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000316	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000766	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0002967	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000268	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000179	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000465	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000006	PMID:17603483	PCS					I	HPO:probinson[2013-01-09]
OMIM:611554	Leopard syndrome 2		HP:0000369	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:611554	Leopard syndrome 2		HP:0000303	PMID:17603483	PCS					P	HPO:probinson[2013-04-06]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0003676	OMIM:182601	IEA					C	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0002166	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000020	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0002064	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0002061	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000639	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000716	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0010550	OMIM:182601	TAS					P	HPO:probinson[2012-04-28]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0007340	OMIM:182601	TAS					P	HPO:skoehler[2012-10-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000718	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0003828	OMIM:182601	IEA					M	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0002839	OMIM:182601	IEA					P	HPO:skoehler[2010-06-18]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000734	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000713	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0001249	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0003743	OMIM:182601	IEA					I	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0001347	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0002314	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0003587	OMIM:182601	IEA					C	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000012	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0002354	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0003487	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000726	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0003419	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000741	OMIM:182601	IEA					P	HPO:iea[2009-02-17]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0001258	OMIM:182601	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182601	Spastic paraplegia 4, autosomal dominant		HP:0000006	OMIM:182601	IEA					I	HPO:iea[2009-02-17]
OMIM:253590	Muscular dystrophy, adult-onset, with leukoencephalopathy		HP:0001250	OMIM:253590	IEA					P	HPO:iea[2009-02-17]
OMIM:253590	Muscular dystrophy, adult-onset, with leukoencephalopathy		HP:0002066	OMIM:253590	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253590	Muscular dystrophy, adult-onset, with leukoencephalopathy		HP:0002352	OMIM:253590	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253590	Muscular dystrophy, adult-onset, with leukoencephalopathy		HP:0003560	OMIM:253590	IEA					P	HPO:skoehler[2015-01-21]
OMIM:253590	Muscular dystrophy, adult-onset, with leukoencephalopathy		HP:0000007	OMIM:253590	IEA					I	HPO:iea[2009-02-17]
OMIM:253590	Muscular dystrophy, adult-onset, with leukoencephalopathy		HP:0001324	OMIM:253590	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600459	Arterial dissection with lentiginosis		HP:0001003	OMIM:600459	IEA					P	HPO:iea[2009-02-17]
OMIM:600459	Arterial dissection with lentiginosis		HP:0012180	OMIM:600459	TAS					P	HPO:skoehler[2013-06-13]
OMIM:600459	Arterial dissection with lentiginosis		HP:0000007	OMIM:600459	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:600459	Arterial dissection with lentiginosis		HP:0005294	OMIM:600459	IEA					P	HPO:iea[2009-02-17]
OMIM:617125	Intellectual developmental disorder, autosomal recessive 56		HP:0000007	PMID:21734151	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-10]
OMIM:617125	Intellectual developmental disorder, autosomal recessive 56		HP:0001249	PMID:21734151	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-10]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0001320	PMID:36197437	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0003577	PMID:36197437	PCS		3/5			C	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0001792	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000684	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0001250	PMID:36197437	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0001263	PMID:36197437	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0003593	PMID:36197437	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0008070	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0001808	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0006480	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000518	PMID:36197437	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000958	PMID:36197437	PCS		3/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0011463	PMID:36197437	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0007385	PMID:36197437	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000729	PMID:36197437	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0006297	PMID:36197437	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000965	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000998	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000668	PMID:36197437	PCS		1/11			P	HPO:probinson[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0008897	PMID:36197437	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0200012	PMID:36197437	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0001511	PMID:36197437	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:620789	Aplasia cutis-enamel dysplasia syndrome		HP:0000006	PMID:36197437	PCS					I	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:233270	Gombo syndrome		HP:0000252	OMIM:233270	IEA					P	HPO:iea[2009-02-17]
OMIM:233270	Gombo syndrome		HP:0001156	OMIM:233270	IEA					P	HPO:iea[2009-02-17]
OMIM:233270	Gombo syndrome		HP:0000007	OMIM:233270	IEA					I	HPO:iea[2009-02-17]
OMIM:233270	Gombo syndrome		HP:0000568	OMIM:233270	IEA					P	HPO:iea[2009-02-17]
OMIM:233270	Gombo syndrome		HP:0030680	OMIM:233270	IEA					P	HPO:iea[2009-02-17]
OMIM:233270	Gombo syndrome		HP:0009466	OMIM:233270	IEA					P	HPO:iea[2009-02-17]
OMIM:233270	Gombo syndrome		HP:0001627	OMIM:233270	TAS					P	HPO:skoehler[2015-12-30]
OMIM:233270	Gombo syndrome		HP:0000823	OMIM:233270	IEA					P	HPO:iea[2009-02-17]
OMIM:233270	Gombo syndrome		HP:0030084	OMIM:233270	TAS					P	HPO:skoehler[2014-09-21]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0003577	PMID:22052856;PMID:19648921	PCS		23/23			C	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000023	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0010648	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0002021	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0001371	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0008070	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000939	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000518	PMID:19648921	PCS		2/22			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000418	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0011220	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000938	PMID:19648921	PCS		10/11			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000239	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000316	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0001763	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000358	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0001249	PMID:22052856;PMID:19648921	PCS		22/23			P	HPO:probinson[2022-07-17];HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000973	PMID:19648921	PCS		22/22			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0009904	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0002213	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000233	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000750	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000430	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000490	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0001087	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000592	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0045025	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0007392	PMID:19648921	PCS		22/22			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0002827	PMID:22052856;PMID:19648921	PCS		15/22			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000007	PMID:19648921	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0001511	PMID:19648921	PCS		18/20			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0001015	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0002987	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0002305	PMID:22052856;PMID:19648921	PCS		5/23			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000325	PMID:19648921	PCS					P	HPO:probinson[2022-07-17];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000963	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000501	PMID:22052856	PCS		1/1			P	HPO:probinson[2022-07-17]
OMIM:614438	Cutis laxa, autosomal recessive, type IIIB		HP:0000028	PMID:22052856	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-17]
OMIM:615726	Pachyonychia congenita 3		HP:0000230	OMIM:615726	TAS					P	HPO:skoehler[2015-09-11]
OMIM:615726	Pachyonychia congenita 3		HP:0000221	OMIM:615726	TAS					P	HPO:skoehler[2015-09-11]
OMIM:615726	Pachyonychia congenita 3		HP:0000975	OMIM:615726	TAS					P	HPO:skoehler[2015-09-11]
OMIM:615726	Pachyonychia congenita 3		HP:0008401	PMID:7545493	PCS		3/3			P	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615726	Pachyonychia congenita 3		HP:0008404	PMID:24611874	PCS		3/3			P	HPO:skoehler[2015-09-11];HPO:probinson[2020-07-17];HPO:probinson[2022-04-11]
OMIM:615726	Pachyonychia congenita 3		HP:0007556	PMID:7545493	PCS					P	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615726	Pachyonychia congenita 3		HP:0000982	PMID:7545493;PMID:11886499	PCS		6/10			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615726	Pachyonychia congenita 3		HP:0002745	PMID:7545493;PMID:11886499	PCS		7/10			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615726	Pachyonychia congenita 3		HP:0007502	PMID:11886499	PCS		1/7			P	HPO:probinson[2022-04-11]
OMIM:615726	Pachyonychia congenita 3		HP:0040181	OMIM:615726	TAS					P	HPO:skoehler[2015-09-11]
OMIM:615726	Pachyonychia congenita 3		HP:0000006	PMID:24611874	PCS					I	HPO:probinson[2020-07-17]
OMIM:615726	Pachyonychia congenita 3		HP:0010765	PMID:7545493	PCS					P	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615040	Episodic pain syndrome, familial, 1		HP:0003593	PMID:20547126	PCS					C	HPO:skoehler[2013-06-05];HPO:probinson[2023-03-01]
OMIM:615040	Episodic pain syndrome, familial, 1		HP:0032148	PMID:20547126	PCS				HP:0025212	P	HPO:probinson[2023-03-01]
OMIM:615040	Episodic pain syndrome, familial, 1		HP:0000006	PMID:20547126	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2023-03-01]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0003577	OMIM:605253	TAS					C	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0003431	OMIM:605253	TAS				HP:0012828	P	HPO:probinson[2012-03-13]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0003693	OMIM:605253	TAS					P	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0003484	OMIM:605253	TAS					P	HPO:probinson[2012-03-13]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0003383	OMIM:605253	TAS					P	HPO:probinson[2012-03-13]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0001284	OMIM:605253	TAS					P	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0002460	OMIM:605253	TAS					P	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0001270	OMIM:605253	TAS					P	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0001291	OMIM:605253	TAS					P	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0002093	OMIM:605253	IEA					P	HPO:skoehler[2019-09-07]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0007182	OMIM:605253	TAS				HP:0012828	P	HPO:probinson[2012-03-13]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0009830	OMIM:605253	TAS					P	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0000007	OMIM:605253	TAS					I	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0001319	OMIM:605253	TAS					P	HPO:probinson[2009-02-17]
OMIM:605253	Neuropathy, congenital hypomyelinating, 1, autosomal recessive		HP:0000006	OMIM:605253	TAS					I	HPO:probinson[2009-02-17]
OMIM:603622	Deafness, autosomal dominant nonsyndromic sensorineural 17		HP:0003621	OMIM:603622	TAS					C	HPO:skoehler[2009-02-17]
OMIM:603622	Deafness, autosomal dominant nonsyndromic sensorineural 17		HP:0005101	OMIM:603622	TAS					P	HPO:skoehler[2009-02-17]
OMIM:603622	Deafness, autosomal dominant nonsyndromic sensorineural 17		HP:0000006	OMIM:603622	TAS					I	HPO:skoehler[2009-02-17]
OMIM:618564	Microangiopathy and leukoencephalopathy, pontine, autosomal dominant		HP:0100543	PMID:27666438	PCS		9/18			P	HPO:probinson[2019-10-05]
OMIM:618564	Microangiopathy and leukoencephalopathy, pontine, autosomal dominant		HP:0003596	PMID:27666438	PCS		3/5			C	HPO:probinson[2022-08-11]
OMIM:618564	Microangiopathy and leukoencephalopathy, pontine, autosomal dominant		HP:0000726	PMID:27666438	PCS		1/18			P	HPO:probinson[2019-10-05]
OMIM:618564	Microangiopathy and leukoencephalopathy, pontine, autosomal dominant		HP:0011462	PMID:27666438	PCS		2/5			C	HPO:probinson[2022-08-11]
OMIM:618564	Microangiopathy and leukoencephalopathy, pontine, autosomal dominant		HP:0030890	PMID:27666438	PCS		18/18			P	HPO:probinson[2019-10-05]
OMIM:618564	Microangiopathy and leukoencephalopathy, pontine, autosomal dominant		HP:0002172	PMID:27666438	PCS		6/15			P	HPO:probinson[2019-10-05]
OMIM:618564	Microangiopathy and leukoencephalopathy, pontine, autosomal dominant		HP:0000006	PMID:27666438	PCS					I	HPO:probinson[2019-10-05];HPO:probinson[2019-10-05]
OMIM:245480	Specific granule deficiency		HP:0003593	PMID:11313242	PCS		1/1			C	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0041042	OMIM:245480	TAS					P	HPO:probinson[2019-09-07]
OMIM:245480	Specific granule deficiency		HP:0041043	OMIM:245480	TAS					P	HPO:probinson[2019-09-07]
OMIM:245480	Specific granule deficiency		HP:0011993	PMID:10359588;PMID:11313242	PCS		11/11			P	HP:probinson[2018-10-20];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0011447	PMID:11313242	PCS		1/1			P	HPO:probinson[2014-01-01]
OMIM:245480	Specific granule deficiency		HP:0012551	PMID:10359588;PMID:11313242	PCS		2/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08];HPO:probinson[2014-01-01];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0011991	PMID:11313242	PCS		0/1			P	HPO:probinson[2014-01-01];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0041046	OMIM:245480	TAS					P	HPO:probinson[2019-09-07]
OMIM:245480	Specific granule deficiency		HP:0041044	PMID:11313242	PCS		1/1			P	HPO:probinson[2019-09-07];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0002718	PMID:11313242	PCS		11/11			P	HP:probinson[2018-10-20];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0041045	OMIM:245480	TAS					P	HPO:probinson[2019-09-07]
OMIM:245480	Specific granule deficiency		HP:0000403	PMID:11313242	PCS		1/1			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0000007	PMID:11313242	PCS					I	HPO:probinson[2009-02-17];HP:probinson[2018-10-20]
OMIM:245480	Specific granule deficiency		HP:0006532	PMID:11313242	PCS		1/1			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:245480	Specific granule deficiency		HP:0040238	PMID:11313242	PCS		1/1			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000341	PMID:25748484	PCS		1/2			P	HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000343	PMID:25748484	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0004322	PMID:25748484	PCS		1/2			P	HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0003198	PMID:25748484	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0001371	OMIM:616549	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0008807	OMIM:616549	TAS				HP:0012832	P	HPO:skoehler[2015-12-30]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0002162	PMID:25748484	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0001290	PMID:25748484	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0001270	PMID:25748484	PCS		1/2			P	HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000414	PMID:25748484	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000219	PMID:25748484	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000218	PMID:25748484	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000252	PMID:25748484	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000430	PMID:25748484	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000232	PMID:25748484	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000470	OMIM:616549	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000508	PMID:25748484	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000007	PMID:25748484	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0002944	OMIM:616549	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0001638	OMIM:616549	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000465	PMID:25748484	PCS	HP:0003577	2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0003798	PMID:25748484	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000347	PMID:25748484	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0000369	PMID:25748484	PCS	HP:0003577	1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616549	Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism		HP:0004602	PMID:25748484	PCS	HP:0003577	2/2			P	HPO:probinson[2020-09-12]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0003676	PMID:21092922	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0002587	OMIM:260600	IEA					P	HPO:iea[2009-02-17]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0001250	PMID:21092922	PCS		2/5			P	HPO:skoehler[2012-11-28];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0030211	PMID:21092922	PCS		3/4			P	HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0002283	PMID:21092922	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0003593	PMID:21092922	PCS		7/7			C	HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0000280	PMID:21092922	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0001508	PMID:21092922	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0000639	PMID:21092922	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0001522	OMIM:260600	IEA					C	HPO:iea[2009-02-17]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0002415	OMIM:260600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0002313	PMID:21092922	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0000577	PMID:21092922	PCS		2/4			P	HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0001622	OMIM:260600	IEA					P	HPO:iea[2009-02-17]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0008936	PMID:21092922	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0002751	PMID:21092922	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0000252	PMID:21092922	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0003269	OMIM:260600	IEA					P	HPO:iea[2009-02-17]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0001344	PMID:21092922	PCS		7/7			P	HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0002353	PMID:21092922	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0001263	PMID:21092922	PCS		7/7		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0006918	OMIM:260600	IEA					P	HPO:iea[2009-02-17]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0034392	PMID:21092922	PCS		6/7			P	HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0007371	PMID:21092922	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0034353	PMID:21092922	PCS		7/7			P	HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0007210	PMID:21092922	PCS		6/7			P	HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0007256	PMID:21092922	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0000007	PMID:21092922	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:260600	Leukodystrophy, hypomyelinating, 3		HP:0000505	PMID:21092922	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0004743	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0003774	PMID:22019273	PCS	HP:0011463	1/1			P	HPO:skoehler[2013-05-29];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0003577	PMID:22019273	PCS		1/1			C	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0003016	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0008905	PMID:22019273	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0001773	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0001156	PMID:22019273	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000023	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000089	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0004322	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0002240	PMID:22019273	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0006371	PMID:22019273	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000518	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0100866	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000219	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000774	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0007843	PMID:22019273	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0002558	PMID:22019273	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000099	PMID:22019273	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000431	PMID:22019273	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000293	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0010454	PMID:22019273	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000093	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0002091	PMID:22019273	PCS		1/1			P	HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0008081	PMID:22019273	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000007	PMID:22019273	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0006644	PMID:22019273	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0000545	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:614376	Short-Rib thoracic dysplasia 5 with or without polydactyly		HP:0003259	PMID:22019273	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-10]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000484	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000750	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0001047	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000581	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0010579	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000506	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000508	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000007	OMIM:606772	IEA					I	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000678	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0001822	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0007663	OMIM:606772	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000505	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000565	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000256	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0006897	OMIM:606772	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0000303	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0001513	OMIM:606772	IEA					P	HPO:iea[2009-02-17]
OMIM:606772	Impaired intellectual development, obesity, mandibular prognathism, and eye and skin anomalies		HP:0001249	OMIM:606772	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0001156	PMID:15805157	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0100864	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0009381	OMIM:609441	TAS				HP:0012828	P	HPO:probinson[2012-06-10]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0010034	PMID:15805157	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0000815	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0008232	PMID:15805157	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0008873	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0009466	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0001769	PMID:15805157	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0009702	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0009803	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0005028	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0009826	PMID:15805157	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0001762	OMIM:609441	IEA					P	HPO:iea[2009-02-17]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0000013	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0002750	PMID:15805157	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0003022	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0002990	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0011969	PMID:15805157	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0009596	PMID:15805157	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0000007	PMID:15805157	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0008368	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0001831	PMID:15805157	PCS		1/1			P	HPO:probinson[2012-06-10];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0000786	PMID:15805157	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:609441	Acromesomelic dysplasia, Demirhan type		HP:0001776	PMID:15805157	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:619652	Immunodeficiency 92		HP:0001894	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0410297	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0030388	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0030991	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0002240	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0020087	PMID:34623332	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0032247	PMID:34623332	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0002090	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0010976	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0100633	PMID:34623332	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0031380	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0011463	PMID:31103457;PMID:34623332	IEA		2/2			C	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0000007	PMID:31103457	PCS					I	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0001954	PMID:34623332	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0030151	PMID:34623332	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0100827	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0002720	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0410028	PMID:34623332	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0004315	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0001974	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0002028	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:619652	Immunodeficiency 92		HP:0002754	PMID:31103457	PCS		1/1			P	HPO:probinson[2022-02-14]
OMIM:264300	Pseudohermaphroditism, male, with gynecomastia		HP:0000771	OMIM:264300	IEA					P	HPO:iea[2009-02-17]
OMIM:264300	Pseudohermaphroditism, male, with gynecomastia		HP:0001939	OMIM:264300	IEA					P	HPO:iea[2009-02-17]
OMIM:264300	Pseudohermaphroditism, male, with gynecomastia		HP:0000789	OMIM:264300	IEA					P	HPO:iea[2009-02-17]
OMIM:264300	Pseudohermaphroditism, male, with gynecomastia		HP:0008730	PMID:10599740	PCS	HP:0003577	15/18			P	HPO:probinson[2020-05-28];HPO:probinson[2020-05-28]
OMIM:264300	Pseudohermaphroditism, male, with gynecomastia		HP:0000007	PMID:10599740	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-05-28]
OMIM:264300	Pseudohermaphroditism, male, with gynecomastia		HP:0000821	OMIM:264300	IEA					P	HPO:iea[2009-02-17]
OMIM:264300	Pseudohermaphroditism, male, with gynecomastia		HP:0000037	OMIM:264300	IEA					P	HPO:iea[2009-02-17]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0000252	PMID:27486776	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-09]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0000750	PMID:32144365	PCS	HP:0003593	1/1			P	HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0001520	PMID:32144365	PCS	HP:0003577	1/1			P	HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0002591	PMID:32144365	PCS	HP:0011463	1/1			P	HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0010442	PMID:27486776	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-09]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0000007	PMID:27486776	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-09]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0000505	PMID:32144365	PCS	HP:0011463	1/1			P	HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0001830	PMID:32144365	PCS	HP:0003577	1/1			P	HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0000510	PMID:27486776	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-09]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0000135	PMID:27486776	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-09]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0000256	PMID:32144365	PCS	HP:0003593	1/1			P	HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0001249	PMID:32144365;PMID:27486776	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-09];HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0001513	PMID:27486776	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-09]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0001513	PMID:32144365	PCS	HP:0011463	1/1			P	HPO:probinson[2021-09-10]
OMIM:617119	Bardet-Biedl syndrome 22		HP:0007988	PMID:32144365	PCS		1/1			P	HPO:probinson[2021-09-10]
OMIM:229200	Brittle cornea syndrome		HP:0000286	OMIM:229200	TAS					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000572	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0007517	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0001374	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0003302	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000365	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000563	OMIM:229200	TAS					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0002650	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0001382	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0002297	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000592	OMIM:229200	TAS					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000481	OMIM:229200	TAS					P	HPO:iea[2014-05-24]
OMIM:229200	Brittle cornea syndrome		HP:0100689	PMID:23642083	PCS					P	HPO:probinson[2014-05-24]
OMIM:229200	Brittle cornea syndrome		HP:0001519	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000987	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0001119	OMIM:229200	TAS					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000007	OMIM:229200	IEA					I	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000703	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000256	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000993	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0000545	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:229200	Brittle cornea syndrome		HP:0001634	OMIM:229200	IEA					P	HPO:iea[2009-02-17]
OMIM:276710	Tyrosinemia, type III		HP:0001250	PMID:10942115	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0003231	PMID:10942115	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0001263	PMID:10942115	PCS		3/5			P	HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0003593	PMID:10942115	PCS		1/3			C	HPO:probinson[2023-02-25];HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0003161	PMID:10942115	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0000007	PMID:10942115	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0003607	PMID:10942115	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0002910	PMID:10942115	PCS		0/5			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-25]
OMIM:276710	Tyrosinemia, type III		HP:0003623	PMID:10942115	PCS		2/3			C	HPO:probinson[2023-02-25]
OMIM:269630	Second metatarsal-metacarpal syndrome		HP:0000926	OMIM:269630	IEA					P	HPO:iea[2009-02-17]
OMIM:269630	Second metatarsal-metacarpal syndrome		HP:0000007	OMIM:269630	IEA					I	HPO:iea[2009-02-17]
OMIM:269630	Second metatarsal-metacarpal syndrome		HP:0005916	OMIM:269630	TAS					P	HPO:probinson[2022-04-07]
OMIM:269630	Second metatarsal-metacarpal syndrome		HP:0100266	OMIM:269630	IEA					P	HPO:iea[2009-02-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0002344	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0003676	OMIM:612075	TAS					C	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0003577	PMID:17486094	PCS		2/7			C	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0003355	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0001250	PMID:17486094	PCS		2/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0002066	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0001252	OMIM:612075	TAS					P	HPO:skoehler[2014-11-26]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0001290	OMIM:612075	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0001508	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0001824	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0000114	PMID:17486094	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0001249	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0003623	PMID:17486094	PCS		5/7			C	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0003128	PMID:17486094	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0002014	PMID:17486094	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0008936	PMID:17486094	PCS		7/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0002133	PMID:17486094	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0002013	PMID:17486094	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0002098	PMID:17486094	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0011968	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0002490	PMID:17486094	PCS		2/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0000007	PMID:17486094	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0008347	PMID:17486094	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0004900	PMID:17486094	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0000544	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612075	Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)		HP:0004326	OMIM:612075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0003577	PMID:23692737	PCS		3/5			C	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0001058	PMID:23692737	PCS		2/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0004322	PMID:23692737	PCS		2/4			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0010648	PMID:23692737	PCS		5/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0001382	PMID:23692737	PCS		5/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0001373	PMID:23692737	PCS		2/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0000592	PMID:23692737	PCS		5/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0001290	PMID:23692737	PCS		3/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0011463	PMID:23692737	PCS		2/5			C	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0025019	PMID:23692737	PCS		1/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0000978	PMID:23692737	PCS		5/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0002757	PMID:23692737	PCS		4/5			P	HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0000006	PMID:23692737	PCS					I	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619120	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2		HP:0000974	PMID:23692737	PCS		5/5			P	HPO:probinson[2021-01-30]
OMIM:606766	Spermatogenic failure 3		HP:0003251	PMID:23582645	PCS		3/3			P	HPO:probinson[2022-06-23]
OMIM:606766	Spermatogenic failure 3		HP:0011462	PMID:23582645	PCS		3/3			C	HPO:probinson[2022-06-23]
OMIM:606766	Spermatogenic failure 3		HP:0012207	PMID:23582645	PCS		3/3			P	HPO:probinson[2022-06-23]
OMIM:606766	Spermatogenic failure 3		HP:0000006	PMID:23582645	PCS					I	HPO:skoehler[2013-07-17];HPO:probinson[2022-06-23]
OMIM:619646	Spermatogenic failure 60		HP:0003251	PMID:33211200;PMID:32741963	PCS		4/4			P	HPO:probinson[2022-02-08]
OMIM:619646	Spermatogenic failure 60		HP:0011462	PMID:32741963	PCS		2/2			C	HPO:probinson[2022-02-08]
OMIM:619646	Spermatogenic failure 60		HP:0000007	PMID:32741963	PCS					I	HPO:probinson[2022-02-08]
OMIM:619646	Spermatogenic failure 60		HP:0031038	PMID:33211200;PMID:32741963	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619646	Spermatogenic failure 60		HP:0011961	PMID:33211200;PMID:32741963	PCS		4/4			P	HPO:probinson[2022-02-08]
OMIM:612713	Kahrizi syndrome		HP:0003577	PMID:18781183	PCS		2/3			C	HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0000431	PMID:18781183	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0004322	PMID:18781183	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0001250	PMID:18781183	PCS		0/3			P	HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0003593	PMID:18781183	PCS		1/3			C	HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0001270	PMID:18781183	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0006380	PMID:18781183	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0000518	PMID:18781183	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0012471	PMID:18781183	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0000007	PMID:20700148	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0000414	PMID:18781183	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0000612	PMID:18781183	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0000329	PMID:18781183	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0002942	PMID:18781183	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-22]
OMIM:612713	Kahrizi syndrome		HP:0034391	PMID:18781183	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0010529	PMID:24403049	PCS		1/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0003112	PMID:24403049	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0001212	PMID:24403049	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0001773	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0001574	OMIM:266265	IEA					P	HPO:iea[2009-02-17]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0003355	PMID:24403049	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0001156	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0001992	PMID:24403049	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0004322	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0002120	OMIM:266265	IEA					P	HPO:iea[2009-02-17]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0001252	OMIM:266265	IEA					P	HPO:iea[2009-02-17]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0030352	PMID:24403049	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0003593	PMID:24403049	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000280	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0011950	PMID:24403049	PCS		1/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0011897	PMID:24403049	PCS		0/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000739	PMID:24403049	PCS		1/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000717	PMID:24403049	PCS		1/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0008155	PMID:24403049	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0010471	PMID:24403049	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000414	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000252	OMIM:266265	IEA					P	HPO:iea[2009-02-17]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000750	PMID:24403049	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0005400	OMIM:266265	IEA					P	HPO:iea[2009-02-17]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0002373	PMID:24403049	PCS		1/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0001263	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0002090	OMIM:266265	IEA					P	HPO:iea[2009-02-17]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000704	OMIM:266265	IEA					P	HPO:iea[2009-02-17]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000729	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0100658	OMIM:266265	IEA					P	HPO:skoehler[2018-10-08]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000349	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000007	PMID:24403049;OMIM:266265	PCS		20/20			I	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000722	PMID:24403049	PCS		1/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0000403	PMID:24403049	PCS		2/2			P	HPO:lccarmody[2017-06-21]
OMIM:266265	Congenital disorder of glycosylation, type IIc		HP:0200055	PMID:24403049	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-13]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0008619	OMIM:124950	IEA					P	HPO:skoehler[2010-06-18]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0004950	OMIM:124950	IEA					P	HPO:iea[2009-02-17]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0001085	OMIM:124950	IEA					P	HPO:iea[2009-02-17]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0008043	OMIM:124950	IEA					P	HPO:iea[2009-02-17]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0001271	OMIM:124950	IEA					P	HPO:iea[2009-02-17]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0011120	OMIM:124950	TAS				HP:0012825	P	HPO:probinson[2012-07-16]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0002922	OMIM:124950	TAS					P	HPO:probinson[2012-07-16]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0000988	OMIM:124950	IEA					P	HPO:iea[2009-02-17]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0002315	OMIM:124950	IEA					P	HPO:iea[2009-02-17]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0001730	OMIM:124950	IEA					P	HPO:iea[2009-02-17]
OMIM:124950	Deafness, sensorineural, with peripheral neuropathy and arterial disease		HP:0000006	OMIM:124950	IEA					I	HPO:iea[2009-02-17]
OMIM:207300	Antithrombin, familial hemorrhagic diathesis due to		HP:0001892	OMIM:207300	TAS					P	HPO:probinson[2009-02-17]
OMIM:207300	Antithrombin, familial hemorrhagic diathesis due to		HP:0000007	OMIM:207300	TAS					I	HPO:probinson[2013-03-10]
OMIM:620548	Premature ovarian failure 22		HP:0008209	PMID:35587281	PCS	HP:0011462	1/1			P	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0008209	PMID:35708642	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0025708	PMID:35587281	PCS		1/1			C	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0000869	PMID:35708642	PCS	HP:0025709	2/2			P	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0008222	PMID:35587281	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0011462	PMID:35708642	PCS		2/2			C	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0008232	PMID:35708642	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0000007	PMID:35587281	PCS					I	HPO:probinson[2024-03-08]
OMIM:620548	Premature ovarian failure 22		HP:0031103	PMID:35708642	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003577	PMID:20839240	PCS		16/17			C	HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0010628	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0002089	OMIM:255320	TAS					P	HPO:skoehler[2015-05-31]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001252	PMID:20839240	PCS		16/17			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001270	PMID:12719381	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0040081	PMID:12719381	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0011463	PMID:20839240	IEA		1/17			C	HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0009025	OMIM:255320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0009046	PMID:20839240	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0008872	PMID:20839240	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001789	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0000218	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003327	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003789	PMID:12719381	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003701	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003787	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003623	PMID:12719381	PCS		1/1			C	HPO:skoehler[2013-01-22]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0002058	OMIM:255320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003202	PMID:12719381	PCS		1/1			P	HPO:skoehler[2013-01-22]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003687	PMID:12719381;PMID:20839240	PCS		11/11			P	HPO:probinson[2024-03-09];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003324	PMID:12719381	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001561	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0002650	PMID:12719381;PMID:20839240	PCS		4/18			P	HPO:probinson[2024-03-09];HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001382	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001284	OMIM:255320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003560	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0002093	PMID:12719381	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0000508	OMIM:255320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003738	OMIM:255320	IEA					P	HPO:iea[2009-02-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0000007	PMID:20839240	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001558	PMID:20839240	PCS	HP:0011461	11/17			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0001319	PMID:12719381	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0002205	PMID:20839240	PCS		9/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003798	OMIM:255320	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0000544	PMID:20839240	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:255320	Minicore myopathy with external ophthalmoplegia		HP:0003557	PMID:12719381	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0002521	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0000574	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0001250	OMIM:616944	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0001252	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0001263	PMID:25102098	PCS		1/1			P	HPO:probinson[2017-06-23];HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0003593	PMID:25102098	PCS		1/1			C	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0011097	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0032792	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0000729	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0000637	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0002714	PMID:25102098	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0001249	PMID:25102098	PCS		1/1			P	HPO:probinson[2017-06-23]
OMIM:616944	Intellectual developmental disorder, autosomal dominant 41		HP:0000006	PMID:25102098	PCS					I	HPO:probinson[2017-06-23]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001276	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0010648	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000023	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000260	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0002240	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001270	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0045075	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0008070	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0040081	PMID:38592547	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0009064	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0011220	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000519	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000316	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0002910	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000494	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000695	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0002155	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001344	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0005484	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0011344	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0012385	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0034197	PMID:38592547	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001518	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000821	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000007	PMID:38592547	PCS					I	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001698	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001511	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001873	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000369	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0000325	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:621130	Fischer-Zirnsak progeroid syndrome		HP:0001974	PMID:38592547	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618969	Immunodeficiency 70		HP:0025188	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0002850	PMID:32499645	PCS		1/3			P	HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0004313	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0020083	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0002571	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0002583	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0003460	PMID:32499645	PCS		1/3			P	HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0033004	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0033005	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0011108	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0010976	PMID:32499645	PCS		1/4			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0012432	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0032132	PMID:32499645	PCS		1/3			P	HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0002608	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0200043	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0000006	PMID:32499645	PCS					I	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618969	Immunodeficiency 70		HP:0002721	PMID:32499645	PCS					P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0008936	PMID:23643384	PCS		8/10			P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0003676	PMID:23643384	PCS					C	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0001264	PMID:23643384	PCS		3/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0002144	PMID:23643384	PCS		1/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0003487	PMID:23643384	PCS		10/10			P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0002079	PMID:23643384	PCS		8/10			P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0001250	PMID:23643384	PCS		2/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0002352	PMID:23643384	PCS					P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0003298	PMID:23643384	PCS		1/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0001260	PMID:23643384	PCS		3/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0003593	PMID:23643384	PCS		9/10			C	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0010729	PMID:23643384	PCS		1/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0001251	PMID:23643384	IEA		4/9			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0002061	PMID:23643384	PCS		10/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0001270	PMID:23643384	PCS		3/10			P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0000639	PMID:23643384	PCS		5/10			P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0011463	PMID:23643384	PCS		1/10			C	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0000737	PMID:23643384	PCS		2/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0000007	PMID:23643384	PCS					I	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0003429	PMID:23643384	PCS		5/9			P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0000543	PMID:23643384	PCS		3/10			P	HPO:probinson[2021-07-16]
OMIM:615281	Hypomyelination with brainstem and spinal cord involvement and legspasticity		HP:0001348	PMID:23643384	PCS		10/10			P	HPO:probinson[2021-07-16]
OMIM:616950	Spermatogenic failure 15		HP:0030346	PMID:25899990;PMID:35718780	PCS		0/4			P	HPO:probinson[2022-06-20]
OMIM:616950	Spermatogenic failure 15		HP:0030345	PMID:25899990;PMID:35718780	PCS		0/4			P	HPO:probinson[2022-06-20]
OMIM:616950	Spermatogenic failure 15		HP:0003251	PMID:25899990;PMID:35718780	PCS		4/4			P	HPO:probinson[2022-06-20]
OMIM:616950	Spermatogenic failure 15		HP:0011462	PMID:25899990;PMID:35718780	PCS		4/4			C	HPO:probinson[2022-06-20]
OMIM:616950	Spermatogenic failure 15		HP:0030087	PMID:35718780	PCS		0/2			P	HPO:probinson[2022-06-20]
OMIM:616950	Spermatogenic failure 15		HP:0000007	PMID:25899990	PCS					I	HPO:probinson[2017-06-25]
OMIM:616950	Spermatogenic failure 15		HP:0031038	PMID:25899990	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:616950	Spermatogenic failure 15		HP:0011961	PMID:25899990;PMID:35718780	PCS		4/4			P	HPO:probinson[2022-06-20];HPO:probinson[2017-06-25];HPO:probinson[2022-06-20]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0002113	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0001880	OMIM:607685	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0001442	OMIM:607685	IEA					I	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0002240	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0000707	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0001723	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0000989	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0004936	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0006685	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0003745	OMIM:607685	IEA					I	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0001744	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0003326	OMIM:607685	IEA					P	HPO:iea[2009-02-17]
OMIM:607685	Hypereosinophilic syndrome, idiopathic		HP:0005547	OMIM:607685	TAS					P	HPO:skoehler[2010-06-20]
OMIM:616788	Orofacial cleft 15		HP:0000286	PMID:25954033	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000582	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000023	PMID:25954033	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0012905	PMID:25954033	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0030001	PMID:25954033	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0011800	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0100271	PMID:25954033	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:616788	Orofacial cleft 15		HP:0045075	PMID:25954033	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0100336	PMID:25954033	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0010294	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0100337	PMID:25954033	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0009890	PMID:25954033	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0007651	PMID:25954033	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000316	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000954	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000414	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0009743	PMID:25954033	PCS		0/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000653	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000411	PMID:25954033	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0200153	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000006	PMID:25954033	PCS					I	HPO:probinson[2017-06-18]
OMIM:616788	Orofacial cleft 15		HP:0000369	PMID:25954033	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-15]
OMIM:616788	Orofacial cleft 15		HP:0000028	PMID:25954033	PCS		1/1	MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:621124	Spermatogenic failure 98		HP:0025708	PMID:36593121	PCS		3/3			C	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0033393	PMID:36593121	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:6000135	PMID:36593121	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0034011	PMID:36593121	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0032560	PMID:36593121	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0003251	PMID:36593121	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0012207	PMID:36593121	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0000007	PMID:36593121	PCS					I	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0034811	PMID:36593121	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0000798	PMID:36593121	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0032558	PMID:36593121	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621124	Spermatogenic failure 98		HP:0032559	PMID:36593121	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000044	OMIM:147950	IEA					P	HPO:iea[2009-02-17]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0004322	OMIM:147950	IEA					P	HPO:iea[2009-02-17]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0001274	OMIM:147950	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000938	OMIM:147950	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0003829	OMIM:147950	TAS					I	HPO:skoehler[2015-12-30]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000612	OMIM:147950	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000458	PMID:16606836	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0030680	OMIM:147950	IEA					P	HPO:iea[2009-02-17]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0030084	OMIM:147950	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0001249	OMIM:147950	IEA					P	HPO:iea[2009-02-17]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0009804	PMID:16606836	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000054	OMIM:147950	TAS					P	HPO:skoehler[2014-11-26]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000175	PMID:16606836	PCS		1/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000453	OMIM:147950	IEA					P	HPO:iea[2009-02-17]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000771	OMIM:147950	TAS					P	HPO:skoehler[2015-12-30]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0032466	PMID:16606836	PCS		1/4			P	HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0100257	OMIM:147950	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000407	OMIM:147950	IEA					P	HPO:iea[2009-02-17]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0004409	PMID:16606836	PCS		1/8			P	HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000823	PMID:16606836	PCS		6/8			P	HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0001335	OMIM:147950	TAS					P	HPO:skoehler[2015-12-30]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000028	PMID:16606836	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000204	PMID:16606836	PCS		1/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000006	PMID:12627230	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:147950	Hypogonadotropic hypogonadism 2 with or without anosmia		HP:0000786	OMIM:147950	TAS					P	HPO:skoehler[2014-11-26]
OMIM:242890	Immunoglobulin D level in plasma, low		HP:0002715	OMIM:242890	IEA					P	HPO:iea[2009-02-17]
OMIM:242890	Immunoglobulin D level in plasma, low		HP:0000007	OMIM:242890	IEA					I	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0004325	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0430043	PMID:29456757	PCS		4/4			P	HPO:probinson[2024-08-04]
OMIM:303600	Coffin-Lowry syndrome		HP:0000365	PMID:30740391	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0004322	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0001250	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0001252	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0003196	PMID:30740391	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0003593	PMID:30740391	PCS		1/1			C	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0010049	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000280	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0010761	PMID:30740391	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0011220	PMID:30740391	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0000316	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0000954	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0008454	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0003745	OMIM:303600	TAS					I	HPO:skoehler[2015-12-30]
OMIM:303600	Coffin-Lowry syndrome		HP:0009746	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0001169	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0001763	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0001249	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0002553	OMIM:303600	PCS					P	HPO:probinson[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000494	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0001187	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0000252	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000574	OMIM:303600	PCS					P	HPO:probinson[2012-03-02]
OMIM:303600	Coffin-Lowry syndrome		HP:0009928	PMID:30740391	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0002673	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0002750	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0002035	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0001063	OMIM:303600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:303600	Coffin-Lowry syndrome		HP:0001263	PMID:30740391	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0001182	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0000407	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000965	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0001812	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000767	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000689	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0002868	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000768	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0001653	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000687	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000445	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0010309	OMIM:303600	TAS					P	HPO:skoehler[2013-01-22]
OMIM:303600	Coffin-Lowry syndrome		HP:0001476	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000189	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000463	OMIM:303600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000023	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0002684	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000139	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0002119	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0000218	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000411	PMID:30740391	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0001423	PMID:8955270	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0000179	PMID:30740391	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:303600	Coffin-Lowry syndrome		HP:0000336	OMIM:303600	TAS					P	HPO:skoehler[2015-10-05]
OMIM:303600	Coffin-Lowry syndrome		HP:0000973	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0002650	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000232	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000194	OMIM:303600	TAS					P	HPO:skoehler[2013-01-22]
OMIM:303600	Coffin-Lowry syndrome		HP:0002808	OMIM:303600	IEA					P	HPO:iea[2012-03-02]
OMIM:303600	Coffin-Lowry syndrome		HP:0000506	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0000668	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0002208	OMIM:303600	TAS					P	HPO:skoehler[2013-01-22]
OMIM:303600	Coffin-Lowry syndrome		HP:0000303	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:303600	Coffin-Lowry syndrome		HP:0006129	OMIM:303600	IEA					P	HPO:iea[2009-02-17]
OMIM:300321	Fg syndrome 2		HP:0002003	PMID:17632775	PCS					P	HPO:probinson[2013-03-23]
OMIM:300321	Fg syndrome 2		HP:0004325	OMIM:300321	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300321	Fg syndrome 2		HP:0000750	PMID:17632775	PCS				HP:0012825	P	HPO:probinson[2013-03-23]
OMIM:300321	Fg syndrome 2		HP:0010055	OMIM:300321	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300321	Fg syndrome 2		HP:0011220	OMIM:300321	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300321	Fg syndrome 2		HP:0011246	PMID:17632775	PCS					P	HPO:probinson[2013-03-23]
OMIM:300321	Fg syndrome 2		HP:0001319	PMID:17632775	TAS					P	HPO:probinson[2013-03-23]
OMIM:300321	Fg syndrome 2		HP:0001417	PMID:17632775	PCS					I	HPO:probinson[2013-01-09]
OMIM:300321	Fg syndrome 2		HP:0000411	OMIM:300321	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300321	Fg syndrome 2		HP:0002019	PMID:17632775	PCS					P	HPO:probinson[2013-03-23]
OMIM:300321	Fg syndrome 2		HP:0002236	OMIM:300321	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0000099	PMID:20800271	PCS					P	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0003774	PMID:20800271	PCS					P	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0003676	PMID:20800271	PCS					C	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0033493	PMID:20800271	PCS		8/9			P	HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0012574	PMID:20800271	PCS		8/9			P	HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0025005	PMID:20800271	PCS		8/9			P	HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0000083	PMID:20800271	PCS		15/28			P	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0002907	PMID:20800271	PCS		22/22			P	HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0012576	PMID:20800271	PCS		9/9			P	HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0004746	PMID:20800271	PCS		9/9			P	HPO:probinson[2023-03-24]
OMIM:614809	Nephropathy due to CFHR5 deficiency		HP:0000006	PMID:20800271	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-24]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000066	OMIM:613800	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0003577	PMID:21358632	PCS		3/3			C	HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0004322	PMID:21358632	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0002780	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000160	PMID:21358632	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0002020	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0001508	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000319	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0008551	PMID:21358632	PCS		3/3			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0002779	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000059	OMIM:613800	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000377	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0001620	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000252	PMID:21358632	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0002750	PMID:21358632	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000430	OMIM:613800	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0003561	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0003187	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0011968	PMID:21358632	PCS	HP:0003593	3/3			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0001382	OMIM:613800	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0003100	PMID:21358632	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0012385	OMIM:613800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000007	PMID:21358632	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0006443	PMID:21358632	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0008665	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000268	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0001511	OMIM:613800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613800	Meier-Gorlin syndrome 2		HP:0000347	PMID:21358632;OMIM:613800	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:191480	Uncombable hair syndrome 1		HP:0002235	PMID:27866708	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-14]
OMIM:191480	Uncombable hair syndrome 1		HP:0011463	PMID:27866708	PCS					C	HPO:probinson[2022-06-26]
OMIM:191480	Uncombable hair syndrome 1		HP:0030056	PMID:27866708	PCS					P	HPO:skoehler[2015-01-20];HPO:probinson[2020-07-14]
OMIM:191480	Uncombable hair syndrome 1		HP:0000007	PMID:27866708	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-14]
OMIM:191480	Uncombable hair syndrome 1		HP:0011359	PMID:27866708	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-14]
OMIM:178550	Pulmonary hemosiderosis		HP:0001891	OMIM:178550	IEA					P	HPO:iea[2009-02-17]
OMIM:178550	Pulmonary hemosiderosis		HP:0005828	OMIM:178550	IEA					P	HPO:iea[2009-02-17]
OMIM:178550	Pulmonary hemosiderosis		HP:0002093	OMIM:178550	IEA					P	HPO:iea[2009-02-17]
OMIM:178550	Pulmonary hemosiderosis		HP:0002206	OMIM:178550	IEA					P	HPO:iea[2009-02-17]
OMIM:178550	Pulmonary hemosiderosis		HP:0000006	OMIM:178550	IEA					I	HPO:iea[2009-02-17]
OMIM:178550	Pulmonary hemosiderosis		HP:0006535	OMIM:178550	IEA					P	HPO:iea[2009-02-17]
OMIM:178550	Pulmonary hemosiderosis		HP:0002105	OMIM:178550	IEA					P	HPO:iea[2009-02-17]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000286	PMID:34143952	PCS		6/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000483	PMID:34143952	PCS		2/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000486	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0001052	PMID:34143952	PCS		3/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0001252	PMID:34143952	PCS		6/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0002162	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0002020	PMID:34143952	PCS		3/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0003593	PMID:34143952	PCS					C	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0002280	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0012347	PMID:34143952	PCS		12/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0012471	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000316	PMID:34143952	PCS		2/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000414	PMID:34143952	PCS		6/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0006970	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000219	PMID:34143952	PCS		9/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0009765	PMID:34143952	PCS		4/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000218	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000411	PMID:34143952	PCS		2/12		HP:0012825	P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000278	PMID:34143952	PCS		6/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0001249	PMID:34143952	PCS					P	HPO:probinson[2021-09-24];HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000175	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000494	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000431	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24];HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0001762	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000430	PMID:34143952	PCS		9/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000034	PMID:34143952	PCS		1/4	MALE		P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000490	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000391	PMID:34143952	PCS		3/12			P	HPO:probinson[2021-09-24];HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0001263	PMID:34143952	IEA		12/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0045025	PMID:34143952	PCS		6/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0011470	PMID:34143952	PCS	HP:0003593	2/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000629	PMID:34143952	PCS		1/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000508	PMID:34143952	PCS		2/12			P	HPO:probinson[2021-09-24];HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000007	PMID:34143952	PCS					I	HPO:probinson[2021-09-24];HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000322	PMID:34143952	PCS		6/12			P	HPO:probinson[2021-09-24]
OMIM:619493	Congenital disorder of glycosylation, type 2V		HP:0000369	PMID:34143952	PCS		3/12			P	HPO:probinson[2021-09-24]
OMIM:618955	Retinitis pigmentosa 89		HP:0001133	PMID:32386558	PCS					P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0000662	PMID:32386558	PCS					P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0025158	PMID:32386558	PCS					P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0001395	PMID:32386558	PCS		1/6			P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0030473	PMID:32386558	PCS					P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0002040	PMID:32386558	PCS	HP:0003593	1/6			P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0033149	PMID:32386558	IEA		1/6			P	HPO:probinson[2020-10-13]
OMIM:618955	Retinitis pigmentosa 89		HP:0030329	PMID:32386558	PCS					P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0100259	PMID:32386558	PCS					P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0011463	PMID:32386558	PCS					C	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0001647	PMID:32386558	PCS		1/6			P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0000510	PMID:32386558	PCS					P	HPO:probinson[2020-08-26];HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0001433	PMID:32386558	PCS		1/6			P	HPO:probinson[2020-08-27]
OMIM:618955	Retinitis pigmentosa 89		HP:0000006	PMID:32386558	TAS					I	HPO:probinson[2020-08-26];HPO:probinson[2020-08-26]
OMIM:618955	Retinitis pigmentosa 89		HP:0001413	PMID:32386558	PCS		1/6			P	HPO:probinson[2020-08-27]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002542	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002345	OMIM:183090	TAS					P	HPO:probinson[2012-04-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000640	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002067	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001310	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001151	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0003693	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001272	PMID:17850638	PCS		2/3			P	HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000020	PMID:17850638	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002063	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001252	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001251	PMID:17850638	PCS		3/3			P	HPO:probinson[2022-05-18];HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001290	OMIM:183090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002380	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0011462	PMID:17850638	PCS		2/3			C	HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002839	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000514	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000657	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002317	PMID:17850638	PCS		2/3			P	HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000510	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0003743	OMIM:183090	IEA					I	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001265	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002015	PMID:17850638	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001300	OMIM:183090	IEA					P	HPO:skoehler[2018-10-08]
OMIM:183090	Spinocerebellar ataxia 2		HP:0003487	PMID:17850638	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0003584	PMID:17850638	PCS		1/3			C	HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002495	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001260	PMID:17850638	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002198	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002174	OMIM:183090	TAS					P	HPO:probinson[2012-04-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002075	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002073	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002172	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002070	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000726	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000602	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0002503	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001257	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000641	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:183090	Spinocerebellar ataxia 2		HP:0000006	PMID:8896555	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-18]
OMIM:183090	Spinocerebellar ataxia 2		HP:0001336	OMIM:183090	IEA					P	HPO:iea[2009-02-17]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0002069	PMID:33969125;PMID:15258581	PCS		13/23			P	HPO:probinson[2024-03-09];HPO:probinson[2012-09-20];HPO:probinson[2022-08-19]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0012001	OMIM:254770	TAS					P	HPO:probinson[2012-09-20]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0003621	PMID:33969125	PCS					C	HPO:probinson[2022-08-19]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0002133	OMIM:254770	TAS					P	HPO:probinson[2012-09-20]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0002121	PMID:33969125;PMID:15258581	PCS		14/23			P	HPO:probinson[2024-03-09];HPO:probinson[2012-09-20];HPO:probinson[2022-08-19]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0007000	PMID:33969125	PCS					P	HPO:probinson[2012-09-20];HPO:probinson[2022-08-19]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0032794	PMID:15258581	PCS		10/13			P	HPO:probinson[2024-03-09]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0000006	PMID:15258581	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-18]
OMIM:254770	Myoclonic epilepsy, juvenile, susceptibility to, 1		HP:0001249	PMID:15258581	PCS		0/13			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002188	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001332	PMID:33230297	PCS		7/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001250	PMID:33230297	PCS		3/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000083	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0003073	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000958	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000639	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001409	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0004719	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0006994	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000252	PMID:33230297	PCS		3/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000054	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000010	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001264	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002510	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001344	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001541	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0011968	PMID:33230297	PCS		4/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001263	PMID:33230297	PCS		16/16			P	HP:probinson[2021-10-17];HPO:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000096	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000093	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000969	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001735	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000007	PMID:33230297	PCS					I	HPO:probinson[2021-10-17];HPO:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000648	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001698	PMID:33230297	PCS		3/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000763	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001257	PMID:33230297	PCS		4/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0004722	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001397	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001276	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0003774	PMID:33230297	PCS		3/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001395	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002240	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000939	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001508	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001903	PMID:33230297	PCS		4/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0032263	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000737	PMID:33230297	PCS		7/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001701	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0006895	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001824	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002514	PMID:33230297	PCS		5/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002910	PMID:33230297	PCS		4/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001029	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000533	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002135	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0008936	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002059	PMID:33230297	PCS		3/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0006956	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000750	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0002650	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001285	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001878	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000822	PMID:33230297	PCS		5/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0009830	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000821	PMID:33230297	PCS		5/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001712	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0009710	PMID:33230297	PCS		2/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001511	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0001433	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:619487	Aicardi-Goutieres syndrome 9		HP:0000742	PMID:33230297	PCS		1/16			P	HP:probinson[2021-10-17]
OMIM:206750	Aniridia, partial, with unilateral renal agenesis and psychomotorretardation		HP:0000122	OMIM:206750	IEA					P	HPO:iea[2009-02-17]
OMIM:206750	Aniridia, partial, with unilateral renal agenesis and psychomotorretardation		HP:0000506	OMIM:206750	IEA					P	HPO:iea[2009-02-17]
OMIM:206750	Aniridia, partial, with unilateral renal agenesis and psychomotorretardation		HP:0001087	OMIM:206750	IEA					P	HPO:iea[2009-02-17]
OMIM:206750	Aniridia, partial, with unilateral renal agenesis and psychomotorretardation		HP:0000007	OMIM:206750	IEA					I	HPO:iea[2009-02-17]
OMIM:206750	Aniridia, partial, with unilateral renal agenesis and psychomotorretardation		HP:0000526	OMIM:206750	TAS					P	HPO:probinson[2012-07-21]
OMIM:206750	Aniridia, partial, with unilateral renal agenesis and psychomotorretardation		HP:0002007	OMIM:206750	IEA					P	HPO:iea[2009-02-17]
OMIM:206750	Aniridia, partial, with unilateral renal agenesis and psychomotorretardation		HP:0001249	OMIM:206750	IEA					P	HPO:iea[2009-02-17]
OMIM:123540	Cryofibrinogenemia, familial primary		HP:0001063	OMIM:123540	TAS					P	HPO:probinson[2009-02-17]
OMIM:123540	Cryofibrinogenemia, familial primary		HP:0000790	OMIM:123540	IEA					P	HPO:iea[2009-02-17]
OMIM:123540	Cryofibrinogenemia, familial primary		HP:0008695	OMIM:123540	IEA					P	HPO:iea[2009-02-17]
OMIM:123540	Cryofibrinogenemia, familial primary		HP:0000006	OMIM:123540	IEA					I	HPO:iea[2009-02-17]
OMIM:618014	Premature ovarian failure 14		HP:0011969	PMID:29044499	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:618014	Premature ovarian failure 14		HP:0011462	PMID:29044499	PCS		1/1			C	HPO:probinson[2023-02-09]
OMIM:618014	Premature ovarian failure 14		HP:0008232	PMID:29044499	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:618014	Premature ovarian failure 14		HP:0000007	PMID:29044499	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-09]
OMIM:618014	Premature ovarian failure 14		HP:0008214	PMID:29044499	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:618014	Premature ovarian failure 14		HP:0000786	PMID:29044499	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:610448	Chilblain lupus 1		HP:0003565	PMID:17357087	PCS		1/2			P	HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0001597	OMIM:610448	IEA		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:610448	Chilblain lupus 1		HP:0000992	PMID:17357087	PCS		0/3			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0002829	PMID:17357087	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0007460	PMID:17357087	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0011463	PMID:17357087	PCS		2/3			C	HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0003493	PMID:17357087	PCS		2/2			P	HPO:probinson[2013-12-15];HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0030880	PMID:17357087	PCS		0/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0003593	PMID:17357087	PCS		1/3			C	HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0009710	PMID:17357087	PCS		3/3			P	HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0000006	PMID:17357087	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:610448	Chilblain lupus 1		HP:0200042	PMID:17357087	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0001265	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0003376	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0001761	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0011463	PMID:25152455	PCS		3/3			C	HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0003383	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0001284	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0009027	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0009830	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0000007	PMID:25152455	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0002936	PMID:25152455	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2023-03-12]
OMIM:616039	Charcot-Marie-Tooth disease, recessive intermediate D		HP:0003677	PMID:25152455	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:615530	Parkinson disease 20, early-onset		HP:0008969	PMID:23804577	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0003676	PMID:23804577	PCS					C	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0002067	PMID:23804577	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0001332	PMID:23804577	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0002120	PMID:23804577	PCS		2/2			P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0002362	OMIM:615530	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615530	Parkinson disease 20, early-onset		HP:0025401	PMID:23804577	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0002063	PMID:23804577	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0000658	PMID:23804577	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0025710	PMID:23804577	PCS		1/2			C	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0001621	PMID:23804577	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0001268	PMID:23804577	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0002015	PMID:23804577	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0001300	PMID:23804577	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0001288	PMID:23804577	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0001260	PMID:23804577	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0002172	OMIM:615530	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615530	Parkinson disease 20, early-onset		HP:0012378	PMID:23804577	PCS		1/2			P	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0025709	PMID:23804577	PCS		1/2			C	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0000605	PMID:23804577	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0000007	PMID:23804577	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0007311	PMID:23804577	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0025403	PMID:23804577	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0004305	PMID:23804577	PCS		2/2			P	HPO:probinson[2023-02-27]
OMIM:615530	Parkinson disease 20, early-onset		HP:0001337	PMID:23804577	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-27]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0003202	OMIM:612539	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0001761	OMIM:612539	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0003487	OMIM:612539	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0002395	OMIM:612539	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0002064	OMIM:612539	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0001258	OMIM:612539	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0001324	OMIM:612539	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612539	Spastic paraplegia 42, autosomal dominant		HP:0000006	OMIM:612539	IEA					I	HPO:skoehler[2010-06-19]
OMIM:189230	Toes, space between first and second		HP:0001852	OMIM:189230	IEA					P	HPO:iea[2009-02-17]
OMIM:189230	Toes, space between first and second		HP:0000006	OMIM:189230	IEA					I	HPO:iea[2009-02-17]
OMIM:601223	Neuronal intestinal dysplasia, type B		HP:0001939	OMIM:601223	IEA					P	HPO:iea[2009-02-17]
OMIM:601223	Neuronal intestinal dysplasia, type B		HP:0000006	OMIM:601223	IEA					I	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0007417	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002740	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002840	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002741	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002240	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0100523	PMID:19329991	PCS					P	HPO:probinson[2017-09-04]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002716	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002955	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0006532	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0003206	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0005406	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0001744	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002754	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0003621	OMIM:233700	IEA					C	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0003203	PMID:11133775	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0005224	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0100658	OMIM:233700	TAS					P	HPO:probinson[2017-09-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002726	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0000007	PMID:2011585	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0000964	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002724	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002723	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002742	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002842	OMIM:233700	IEA					P	HPO:iea[2009-02-17]
OMIM:233700	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I		HP:0002721	OMIM:233700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617441	Thrombocytopenia, anemia, and myelofibrosis		HP:0001903	PMID:27743390	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617441	Thrombocytopenia, anemia, and myelofibrosis		HP:0011463	PMID:27743390	PCS		4/4			C	HPO:probinson[2023-02-11]
OMIM:617441	Thrombocytopenia, anemia, and myelofibrosis		HP:0000007	PMID:27743390	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617441	Thrombocytopenia, anemia, and myelofibrosis		HP:0004823	PMID:27743390	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617441	Thrombocytopenia, anemia, and myelofibrosis		HP:0001873	PMID:27743390	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617441	Thrombocytopenia, anemia, and myelofibrosis		HP:0001744	PMID:27743390	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617441	Thrombocytopenia, anemia, and myelofibrosis		HP:0011974	PMID:27743390	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0001342	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0001102	OMIM:177850	TAS					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0002650	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000573	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0025533	OMIM:177850	TAS					P	HPO:skoehler[2017-07-13]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0001681	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000592	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0005462	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0005297	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0012457	OMIM:177850	TAS					P	HPO:probinson[2017-08-26]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0002808	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000608	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000766	OMIM:177850	TAS					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0002705	OMIM:177850	TAS					P	HPO:skoehler[2015-12-30]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0007663	OMIM:177850	TAS					P	HPO:skoehler[2015-07-26]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000505	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000218	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0002634	OMIM:177850	IEA					P	HPO:skoehler[2018-10-08]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0002239	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0004966	OMIM:177850	TAS					P	HPO:probinson[2017-08-26]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0025507	PMID:27933191	PCS					P	HPO:probinson[2017-08-26]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000006	OMIM:177850	IEA					I	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0001634	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:177850	Pseudoxanthoma elasticum, forme fruste		HP:0000545	OMIM:177850	IEA					P	HPO:iea[2009-02-17]
OMIM:619478	Facioscapulohumeral muscular dystrophy 4, digenic		HP:0003484	PMID:27153398	PCS					P	HPO:probinson[2021-10-18]
OMIM:619478	Facioscapulohumeral muscular dystrophy 4, digenic		HP:0003581	PMID:27153398	PCS					C	HPO:probinson[2021-10-18]
OMIM:619478	Facioscapulohumeral muscular dystrophy 4, digenic		HP:0010984	PMID:27153398	PCS					I	HPO:probinson[2021-10-18]
OMIM:619478	Facioscapulohumeral muscular dystrophy 4, digenic		HP:0030319	PMID:27153398	PCS					P	HPO:probinson[2021-10-18]
OMIM:184700	Polycystic ovary syndrome 1		HP:0000141	OMIM:184700	IEA					P	HPO:iea[2009-02-17]
OMIM:184700	Polycystic ovary syndrome 1		HP:0001939	OMIM:184700	IEA					P	HPO:iea[2009-02-17]
OMIM:184700	Polycystic ovary syndrome 1		HP:0008675	OMIM:184700	IEA					P	HPO:iea[2009-02-17]
OMIM:184700	Polycystic ovary syndrome 1		HP:0000876	OMIM:184700	IEA					P	HPO:iea[2009-02-17]
OMIM:184700	Polycystic ovary syndrome 1		HP:0000006	OMIM:184700	IEA					I	HPO:iea[2009-02-17]
OMIM:184700	Polycystic ovary syndrome 1		HP:0001007	OMIM:184700	TAS					P	HPO:probinson[2009-02-17]
OMIM:184700	Polycystic ovary syndrome 1		HP:0001513	OMIM:184700	IEA					P	HPO:iea[2009-02-17]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001250	PMID:31960134	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000160	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001274	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0012104	PMID:31960134	PCS		3/5			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0011220	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000414	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0008872	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001522	PMID:31960134	PCS		3/6			C	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001188	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001561	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000252	PMID:31960134	PCS		4/5			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000233	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0006913	PMID:31960134	PCS		3/5			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001263	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000470	PMID:31960134	PCS		5/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001284	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0005280	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001838	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0003819	PMID:31960134	PCS		1/6			C	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000007	PMID:31960134	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001558	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0002804	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000648	PMID:31960134	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0001257	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000347	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000369	PMID:31960134	PCS		6/6			P	HPO:probinson[2020-05-11]
OMIM:618766	Arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum		HP:0000028	PMID:31960134	PCS		3/3	MALE		P	HPO:probinson[2020-05-11]
OMIM:152420	Lithium transport		HP:0007302	OMIM:152420	TAS					P	HPO:probinson[2009-02-17]
OMIM:152420	Lithium transport		HP:0000006	OMIM:152420	IEA					I	HPO:iea[2009-02-17]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000175	PMID:24075189	PCS		1/7			P	HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0003577	PMID:24075189	PCS		7/7			C	HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0002089	PMID:24075189	PCS		4/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000431	OMIM:615524	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615524	Microphthalmia, syndromic 12		HP:0005156	OMIM:615524	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615524	Microphthalmia, syndromic 12		HP:0001629	OMIM:615524	TAS					P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000528	PMID:24075189	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000007	OMIM:615524	TAS					I	HPO:skoehler[2017-07-13]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000568	PMID:24075189	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000813	PMID:24075189	PCS		2/2	FEMALE		P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000455	OMIM:615524	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615524	Microphthalmia, syndromic 12		HP:0003811	PMID:24075189	PCS		4/5			C	HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000278	OMIM:615524	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000006	PMID:24075189	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000776	PMID:24075189	PCS		6/6			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000028	PMID:24075189	PCS		1/5	MALE		P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0001249	PMID:24075189	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-05-19]
OMIM:615524	Microphthalmia, syndromic 12		HP:0000347	OMIM:615524	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615524	Microphthalmia, syndromic 12		HP:0002566	PMID:24075189	PCS		2/7			P	HPO:probinson[2023-05-19]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0003577	PMID:25168385	PCS		2/2			C	HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0001596	PMID:25168385	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-03-13];HPO:probinson[2024-12-03]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0002299	PMID:25168385	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0025493	PMID:8488878	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0002164	PMID:8488878	IEA		1/1			P	HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0045075	PMID:8488878	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0008070	PMID:8488878	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0032152	PMID:25168385	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0000953	PMID:8488878	IEA		1/1			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0007556	PMID:8488878	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0000982	PMID:25168385	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0000006	PMID:25168385	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0001820	PMID:25168385	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-13]
OMIM:104100	Palmoplantar keratoderma with congenital alopecia		HP:0000962	PMID:25168385	PCS		2/2			P	HPO:probinson[2024-12-03]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0003236	PMID:16575835	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0010628	OMIM:613155	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0002540	PMID:16575835	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0002365	PMID:16575835	PCS		2/2			P	HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0001371	OMIM:613155	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0003593	OMIM:613155	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0002280	OMIM:613155	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000519	OMIM:613155	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000238	PMID:16575835	PCS		3/5			P	HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000158	PMID:16575835	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000556	PMID:16575835	PCS		0/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0001320	PMID:16575835	PCS		5/5			P	HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000252	PMID:16575835	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0001344	PMID:16575835	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0001321	PMID:16575835	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0002079	PMID:16575835	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0001263	OMIM:613155	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0003560	OMIM:613155	TAS		20/20			P	HPO:skoehler[2015-01-19];HPO:skoehler[2013-05-29]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0032046	PMID:16575835	PCS		1/2			P	HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0005162	OMIM:613155	IEA					P	HPO:skoehler[2019-02-22]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0007033	OMIM:613155	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0008981	PMID:16575835	PCS		4/5			P	HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000007	PMID:16575835	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000568	PMID:16575835	PCS		0/5			P	HPO:probinson[2022-11-04]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0001638	OMIM:613155	TAS		HP:0040283			P	HPO:skoehler[2013-02-25]
OMIM:613155	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1		HP:0000545	PMID:16575835	PCS		3/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-04]
OMIM:180200	RETINOBLASTOMA		HP:0000175	OMIM:180200	IEA					P	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0007902	OMIM:180200	IEA					P	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0001442	OMIM:180200	TAS					I	HPO:skoehler[2012-10-17]
OMIM:180200	RETINOBLASTOMA		HP:0009919	OMIM:180200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:180200	RETINOBLASTOMA		HP:0011531	OMIM:180200	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:180200	RETINOBLASTOMA		HP:0010799	OMIM:180200	TAS					P	HPO:skoehler[2015-12-30]
OMIM:180200	RETINOBLASTOMA		HP:0012254	OMIM:180200	TAS					P	HPO:skoehler[2013-04-18]
OMIM:180200	RETINOBLASTOMA		HP:0001909	OMIM:180200	IEA					P	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0002669	OMIM:180200	IEA					P	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0007862	OMIM:180200	IEA					P	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0003745	OMIM:180200	IEA					I	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0000006	OMIM:180200	IEA					I	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0002665	OMIM:180200	IEA					P	HPO:iea[2009-02-17]
OMIM:180200	RETINOBLASTOMA		HP:0000555	OMIM:180200	IEA					P	HPO:iea[2009-02-17]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0003577	PMID:27939640	PCS		10/10			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000343	PMID:27939640;OMIM:617333	PCS		10/20			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000486	PMID:27939640	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0004322	PMID:27939640;OMIM:617333	PCS		2/20			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001250	PMID:27939640	PCS		5/10			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000160	PMID:27939640	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000581	PMID:27939640	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001252	PMID:27939640	PCS		7/8			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0010862	PMID:27939640	PCS		6/8			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0012368	PMID:27939640	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0033725	PMID:27939640	PCS		1/7			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000316	PMID:27939640	PCS		9/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000337	PMID:27939640	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0002714	PMID:27939640	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000311	PMID:27939640	PCS		7/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001249	PMID:27939640	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0003623	PMID:27939640	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000154	PMID:27939640	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000494	PMID:27939640	PCS		4/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000252	PMID:27939640	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000750	PMID:27939640	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001762	PMID:27939640;OMIM:617333	PCS		10/20			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000431	PMID:27939640	PCS		9/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0031936	PMID:27939640	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0011968	PMID:27939640	PCS		4/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001382	PMID:27939640	PCS		6/10			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001263	PMID:27939640	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0002194	PMID:27939640	PCS		9/10			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0012385	OMIM:617333	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0034295	PMID:27939640	PCS		2/10			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000508	PMID:27939640	PCS		6/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0030890	PMID:27939640	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001511	PMID:27939640;OMIM:617333	PCS		2/20			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0001510	OMIM:617333	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000322	PMID:27939640	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000006	PMID:27939640	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0004602	PMID:27939640	PCS		3/10			P	HPO:probinson[2023-05-18]
OMIM:617333	Intellectual developmental disorder with dysmorphic facies and ptosis		HP:0000369	PMID:27939640	PCS		2/10			P	HPO:probinson[2023-05-18]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001058	PMID:30759870;PMID:30548383;PMID:29606302	PCS		7/7			P	HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001252	PMID:30759870;PMID:29606302	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0003593	PMID:30548383;PMID:29606302	PCS		2/4			C	HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0045074	OMIM:618000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0012432	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0011463	PMID:30548383	PCS		1/2			C	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002619	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002616	PMID:30548383;PMID:29606302	PCS		1/4			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000953	PMID:29606302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002933	PMID:29606302	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001488	PMID:29606302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001763	PMID:30759870;PMID:29606302	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000993	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001765	PMID:29606302	PCS		4/4			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0003623	PMID:30759870	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:6000483	PMID:29606302	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000692	PMID:29606302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001382	PMID:30548383	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001582	PMID:30759870;PMID:30548383;PMID:29606302	PCS		7/7			P	HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0031158	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0034943	PMID:29606302	PCS		2/2			P	HPO:probinson[2023-07-18]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0034273	PMID:29606302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0010562	PMID:29606302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002827	PMID:29606302	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0100658	PMID:29606302	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001537	PMID:30759870;PMID:29606302	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000007	PMID:27023906;PMID:29606302	PCS		20/20			I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000400	PMID:29606302	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0003834	PMID:29606302	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002943	PMID:30759870;PMID:29606302	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001015	PMID:30548383	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0004602	PMID:29606302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0003577	PMID:29606302	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002761	PMID:29606302	PCS		4/4			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000023	PMID:29606302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0012727	PMID:29606302	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0030871	PMID:29606302	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0003177	PMID:29606302	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002162	PMID:29606302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001075	PMID:29606302	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001270	PMID:30759870;PMID:29606302	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0100546	PMID:29606302	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000938	PMID:30759870;PMID:29606302	PCS		5/5			P	HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001822	PMID:30759870;PMID:29606302	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000978	PMID:30759870;PMID:30548383;PMID:29606302	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0004419	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000218	PMID:30759870;PMID:29606302	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002758	PMID:29606302	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0004417	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001027	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000974	PMID:30759870;PMID:30548383;PMID:29606302	PCS		7/7			P	HPO:probinson[2022-05-28];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0004976	PMID:29606302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0025232	PMID:29606302	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0005001	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000470	OMIM:618000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0010810	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000704	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0007495	PMID:30548383	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000987	PMID:30548383	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0003419	PMID:30759870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000465	PMID:29606302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000028	PMID:29606302	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0000347	PMID:29606302	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0001634	PMID:30548383;PMID:29606302	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:618000	Ehlers-Danlos syndrome, classic-like, 2		HP:0002643	PMID:30759870;PMID:29606302	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001871	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001250	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001161	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0004099	OMIM:149000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0009380	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0100764	OMIM:149000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001528	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0004947	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0005606	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001159	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0003745	OMIM:149000	IEA					I	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001004	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0000501	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001249	OMIM:149000	IEA					P	HPO:iea[2009-02-17]
OMIM:149000	Klippel-Trenaunay-Weber syndrome		HP:0001028	OMIM:149000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0003621	PMID:10631146	PCS		5/12			C	HPO:probinson[2022-07-10]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0003596	PMID:10631146	PCS		1/12			C	HPO:probinson[2022-07-10]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0011463	PMID:10631146	PCS		1/12			C	HPO:probinson[2022-07-10]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0011462	PMID:10631146	PCS		5/12			C	HPO:probinson[2022-07-10]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0006682	PMID:10631146	PCS		5/12			P	HPO:probinson[2013-03-11]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0011663	PMID:10631146	PCS					P	HPO:probinson[2013-03-11]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0000006	PMID:10631146	PCS					I	HPO:probinson[2013-03-11]
OMIM:604401	Arrhythmogenic right ventricular dysplasia, familial, 6		HP:0001645	PMID:10631146	PCS		2/12			P	HPO:probinson[2013-03-11]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0001166	PMID:24864036	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0006417	OMIM:610474	IEA					P	HPO:iea[2009-02-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000252	PMID:17033969	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000098	PMID:24864036;PMID:17033969	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0002650	PMID:24864036;PMID:17033969	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000365	PMID:24864036	PCS		2/2			P	HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0030431	PMID:17033969	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0001263	PMID:24864036;PMID:17033969	PCS		13/22			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0004570	PMID:17033969	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0012385	PMID:24864036;PMID:17033969	PCS		20/22			P	HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000407	PMID:17033969	PCS		17/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000767	PMID:17033969	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000007	PMID:24864036	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0001836	OMIM:610474	IEA					P	HPO:iea[2009-02-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000218	PMID:24864036	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0000006	PMID:17033969	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:610474	Camptodactyly, tall stature, and hearing loss syndrome		HP:0001249	PMID:24864036;PMID:17033969	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17];HPO:probinson[2023-01-17]
OMIM:616005	Immunodeficiency 36		HP:0002960	OMIM:616005	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:616005	Immunodeficiency 36		HP:0004322	OMIM:616005	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616005	Immunodeficiency 36		HP:0020072	PMID:25133428	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0002783	PMID:25133428	PCS		3/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0003496	PMID:25133428	PCS		3/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0005550	OMIM:616005	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:616005	Immunodeficiency 36		HP:0003593	PMID:25133428	PCS		2/4			C	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0030812	PMID:25133428	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0011463	PMID:25133428	PCS		1/4			C	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0002718	PMID:25133428	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0012191	OMIM:616005	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:616005	Immunodeficiency 36		HP:0001888	OMIM:616005	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616005	Immunodeficiency 36		HP:0030381	PMID:25133428	PCS		3/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0001744	OMIM:616005	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616005	Immunodeficiency 36		HP:0004315	PMID:25133428	PCS		4/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0003621	PMID:25133428	PCS		1/4			C	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0002110	OMIM:616005	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:616005	Immunodeficiency 36		HP:0012758	OMIM:616005	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:616005	Immunodeficiency 36		HP:0032247	PMID:25133428	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0010976	PMID:25133428	PCS		4/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0002788	PMID:25133428	PCS		4/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0001510	OMIM:616005	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616005	Immunodeficiency 36		HP:0000006	PMID:25133428	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0002720	PMID:25133428	PCS		4/4			P	HPO:probinson[2022-09-06]
OMIM:616005	Immunodeficiency 36		HP:0002028	OMIM:616005	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:616005	Immunodeficiency 36		HP:0002721	OMIM:616005	IEA					P	HPO:skoehler[2015-01-27]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0000252	PMID:26573021	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0001332	PMID:26573021	PCS		3/5			P	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0001250	PMID:26573021	PCS		1/4			P	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0001263	PMID:26573021	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0005484	OMIM:616763	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0003593	OMIM:616763	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0001290	PMID:26573021	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0012736	OMIM:616763	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0000639	PMID:26573021	PCS		2/5			P	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0000007	PMID:26573021	PCS					I	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0007204	PMID:26573021	PCS					P	HPO:probinson[2017-06-17]
OMIM:616763	Leukodystrophy and acquired microcephaly with or without dystonia		HP:0002415	OMIM:616763	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600101	Deafness, autosomal dominant nonsyndromic sensorineural 2		HP:0003676	OMIM:600101	TAS					C	HPO:skoehler[2012-10-17]
OMIM:600101	Deafness, autosomal dominant nonsyndromic sensorineural 2		HP:0000365	OMIM:600101	TAS				HP:0012828	P	HPO:probinson[2013-03-30]
OMIM:600101	Deafness, autosomal dominant nonsyndromic sensorineural 2		HP:0000360	OMIM:600101	TAS					P	HPO:skoehler[2012-11-28]
OMIM:600101	Deafness, autosomal dominant nonsyndromic sensorineural 2		HP:0000006	OMIM:600101	IEA					I	HPO:iea[2009-02-17]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0001056	OMIM:300484	TAS					P	HPO:skoehler[2014-11-26]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000175	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000486	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0002100	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0004322	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000161	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0001263	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0010566	OMIM:300484	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0010442	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000506	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0001419	OMIM:300484	TAS					I	HPO:skoehler[2015-12-30]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000316	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000218	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000455	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0001159	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0005736	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0000456	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300484	Orofaciodigital syndrome VIII		HP:0005349	OMIM:300484	TAS					P	HPO:skoehler[2014-07-11]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0001397	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0003233	PMID:10622252	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0001394	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0003074	PMID:10622252	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0100602	OMIM:604367	TAS					H	HPO:skoehler[2013-08-18]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0011462	PMID:10622252	PCS		2/3			C	HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000855	PMID:10622252	PCS		3/3			P	HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0009125	PMID:10622252	PCS		3/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000876	PMID:10622252	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000956	PMID:10622252	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0009800	OMIM:604367	IEA					H	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0001007	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000831	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0003621	PMID:10622252	PCS		1/3			C	HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0002155	PMID:10622252	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000822	PMID:10622252	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0003758	OMIM:604367	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0009017	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0003635	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000147	OMIM:604367	IEA		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0001015	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0005978	PMID:10622252	PCS		3/3			P	HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000006	PMID:10622252	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000842	PMID:10622252	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0002149	OMIM:604367	IEA					P	HPO:iea[2009-02-17]
OMIM:604367	Lipodystrophy, familial partial, type 3		HP:0000786	PMID:10622252	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002366	OMIM:105550	IEA					P	HPO:iea[2009-02-17]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0003202	OMIM:105550	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0007308	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002059	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0001300	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002442	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002145	OMIM:105550	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002186	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002385	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0001260	OMIM:105550	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0003581	PMID:21944778	PCS					C	HPO:probinson[2012-08-05];HPO:probinson[2022-03-28]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002273	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002171	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0000738	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0000716	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0000726	OMIM:105550	IEA					P	HPO:iea[2009-02-17]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0000605	OMIM:105550	TAS		HP:0040283			P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0007354	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0002529	OMIM:105550	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0000746	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0000741	OMIM:105550	TAS					P	HPO:probinson[2012-08-05]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0001324	OMIM:105550	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0000006	PMID:21944778	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:105550	Amyotrophic lateral sclerosis and/or frontotemporal dementia 1		HP:0003678	OMIM:105550	TAS					C	HPO:probinson[2012-08-05]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0004886	PMID:20301361	PCS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002540	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000365	OMIM:312080	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0004322	PMID:20301361	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001332	PMID:3598129	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001250	PMID:25491635;PMID:29486744	PCS		8/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001252	PMID:29486744	PCS	HP:0003623	8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0003593	PMID:30637272;PMID:29486744	PCS		9/9			C	HPO:iea[2009-02-17];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001251	PMID:25491635	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0033725	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000639	PMID:25491635;PMID:29486744	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000716	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0003429	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0007325	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001249	PMID:25491635	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000511	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001265	PMID:3598129	PCS		4/7			P	HPO:iea[2009-02-17]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002356	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001583	OMIM:312080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000252	PMID:29486744	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000012	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001266	PMID:20301361	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001260	PMID:30637272;PMID:20301361	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001263	PMID:30637272;PMID:29486744	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0011400	PMID:3598129	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001419	PMID:20301361	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000648	PMID:30637272	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001258	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001337	PMID:30637272	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0003677	PMID:3598129	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002168	OMIM:312080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002283	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002361	PMID:30637272	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002080	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0100543	PMID:20301361	PCS		HP:0040281			P	HPO:iea[2012-04-24];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001508	PMID:20301361	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0007266	OMIM:312080	TAS					P	HPO:skoehler[2012-11-21]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0001268	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0100709	PMID:20301361	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002478	PMID:20301361	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002599	PMID:30637272	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0006855	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0003269	PMID:3598129	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002015	PMID:30637272;PMID:18485258	PCS		6/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002136	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0002650	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000750	PMID:20301361	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0007256	PMID:3598129	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:312080	Pelizaeus-Merzbacher disease		HP:0000741	PMID:30637272	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:614160	Muscle hypertrophy		HP:0000007	PMID:15215484	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:614160	Muscle hypertrophy		HP:0003712	PMID:15215484	PCS	HP:0003577	1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20];HPO:probinson[2021-09-23]
OMIM:614160	Muscle hypertrophy		HP:0001348	PMID:15215484	PCS		1/1			P	HPO:probinson[2021-09-23]
OMIM:616777	Seckel syndrome 9		HP:0030799	PMID:26595769	PCS		2/3			P	HPO:probinson[2017-05-31]
OMIM:616777	Seckel syndrome 9		HP:0004322	PMID:26595769	PCS		3/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0000062	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0001629	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0011461	PMID:26595769	PCS		3/3			C	HPO:probinson[2022-03-21]
OMIM:616777	Seckel syndrome 9		HP:0000998	PMID:26595769	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-21]
OMIM:616777	Seckel syndrome 9		HP:0008633	OMIM:616777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616777	Seckel syndrome 9		HP:0002119	PMID:26595769	PCS		1/3			P	HPO:probinson[2017-05-31]
OMIM:616777	Seckel syndrome 9		HP:0000411	PMID:26595769	PCS		3/3			P	HPO:probinson[2017-05-31]
OMIM:616777	Seckel syndrome 9		HP:0000776	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0000275	PMID:26595769	PCS		3/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0000252	PMID:26595769	PCS		3/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0001561	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0000010	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0001762	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0000276	PMID:26595769	PCS		3/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0004971	OMIM:616777	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0002099	PMID:26595769	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-21]
OMIM:616777	Seckel syndrome 9		HP:0001263	PMID:26595769	PCS		3/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0001518	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0000007	PMID:26595769	PCS					I	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0001558	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0008665	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0000444	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0000268	PMID:26595769	PCS		2/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0001511	PMID:26595769	PCS		3/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0002205	PMID:26595769	PCS		2/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0001631	OMIM:616777	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616777	Seckel syndrome 9		HP:0000347	PMID:26595769	PCS		3/3			P	HPO:probinson[2016-07-03]
OMIM:616777	Seckel syndrome 9		HP:0009879	PMID:26595769	PCS		2/3			P	HPO:probinson[2016-07-03]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0003212	PMID:32647003	PCS		3/5			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0002110	PMID:32647003	PCS		4/5			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0003593	PMID:32647003	IEA					C	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0012302	PMID:32647003	PCS		1/5			P	HPO:probinson[2020-09-10];HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0032184	PMID:32647003	PCS		4/5			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0002719	PMID:32647003	PCS		5/5			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0032163	PMID:32647003	PCS		1/5			P	HPO:probinson[2020-09-10];HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0100759	PMID:32647003	PCS		1/4			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0000007	PMID:32647003	PCS					I	HPO:probinson[2020-09-10];HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0002716	PMID:32647003	PCS		5/5			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0000403	PMID:32647003	PCS					P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0001433	PMID:32647003	PCS		5/5			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0003237	PMID:32647003	PCS		3/5			P	HPO:probinson[2020-09-10]
OMIM:618982	Immunodeficiency 72 with autoinflammation		HP:0005404	PMID:32647003	PCS		3/5			P	HPO:probinson[2020-09-10]
OMIM:193240	Vocal cord paralysis and ptosis		HP:0001605	OMIM:193240	TAS					P	HPO:skoehler[2015-01-21]
OMIM:193240	Vocal cord paralysis and ptosis		HP:0001488	OMIM:193240	IEA					P	HPO:iea[2009-02-17]
OMIM:193240	Vocal cord paralysis and ptosis		HP:0000006	OMIM:193240	IEA					I	HPO:iea[2009-02-17]
OMIM:610460	THIOPURINE S-METHYLTRANSFERASE DEFICIENCY		HP:0001871	OMIM:610460	IEA					P	HPO:iea[2009-02-17]
OMIM:610460	THIOPURINE S-METHYLTRANSFERASE DEFICIENCY		HP:0001939	OMIM:610460	IEA					P	HPO:iea[2009-02-17]
OMIM:610460	THIOPURINE S-METHYLTRANSFERASE DEFICIENCY		HP:0000007	OMIM:610460	TAS					I	HPO:iea[2009-02-17]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0002003	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0031846	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0004322	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000160	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000680	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0011712	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0010444	PMID:30905398	PCS		1/2		HP:0012825	P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0002080	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000319	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000855	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0003429	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0001324	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000894	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0001788	PMID:30905398	PCS	HP:0011461	1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000252	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0005144	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0004396	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0011800	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000706	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000668	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0030890	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0003758	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0002645	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0001511	PMID:30905398	PCS	HP:0030674	1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000444	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000586	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000520	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0001015	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0001510	PMID:30905398	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000325	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0004349	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000347	PMID:30905398	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619322	Marbach-Rustad progeroid syndrome		HP:0000006	PMID:30905398	PCS					I	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:212080	Cardiac lipidosis, familial		HP:0000252	OMIM:212080	IEA					P	HPO:iea[2009-02-17]
OMIM:212080	Cardiac lipidosis, familial		HP:0001939	OMIM:212080	IEA					P	HPO:iea[2009-02-17]
OMIM:212080	Cardiac lipidosis, familial		HP:0000007	OMIM:212080	IEA					I	HPO:iea[2009-02-17]
OMIM:212080	Cardiac lipidosis, familial		HP:0001635	OMIM:212080	IEA					P	HPO:iea[2009-02-17]
OMIM:212080	Cardiac lipidosis, familial		HP:0001638	OMIM:212080	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212080	Cardiac lipidosis, familial		HP:0001522	OMIM:212080	IEA					C	HPO:iea[2009-02-17]
OMIM:615518	Immunodeficiency 13		HP:0005403	PMID:22184408	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0002110	PMID:22184408	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0100582	PMID:22184408	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0011945	PMID:22184408	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0011108	PMID:22184408	PCS		2/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0010976	PMID:22184408	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0032275	PMID:22184408	PCS		1/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0033222	PMID:22184408	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0000403	PMID:22184408	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0001888	PMID:22184408	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0006532	PMID:22184408	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0002788	PMID:22184408	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0000006	PMID:22184408	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-30]
OMIM:615518	Immunodeficiency 13		HP:0002721	PMID:22184408	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2021-05-30]
OMIM:260370	Pancreatic agenesis, congenital		HP:0001562	PMID:19496967	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:260370	Pancreatic agenesis, congenital		HP:0003577	PMID:8988180	PCS		1/1			C	HPO:probinson[2022-05-25]
OMIM:260370	Pancreatic agenesis, congenital		HP:0001508	PMID:19496967	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-26]
OMIM:260370	Pancreatic agenesis, congenital		HP:0030795	PMID:19496967	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:260370	Pancreatic agenesis, congenital		HP:0001738	PMID:12970316	PCS	HP:0003623	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-25]
OMIM:260370	Pancreatic agenesis, congenital		HP:0002594	PMID:19496967	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-26]
OMIM:260370	Pancreatic agenesis, congenital		HP:0100801	PMID:8988180	PCS		1/1			P	HPO:probinson[2022-05-25]
OMIM:260370	Pancreatic agenesis, congenital		HP:0011461	PMID:19496967;PMID:12970316	PCS		2/2			C	HPO:probinson[2022-05-25];HPO:probinson[2022-05-26]
OMIM:260370	Pancreatic agenesis, congenital		HP:0000007	PMID:8988180	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-25]
OMIM:260370	Pancreatic agenesis, congenital		HP:0000857	PMID:8988180	PCS	HP:0003623	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-25]
OMIM:260370	Pancreatic agenesis, congenital		HP:0000857	PMID:12970316	PCS		1/1			P	HPO:probinson[2022-05-25]
OMIM:260370	Pancreatic agenesis, congenital		HP:0000857	PMID:19496967	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:260370	Pancreatic agenesis, congenital		HP:0001511	PMID:19496967;PMID:12970316	PCS		2/2			P	HPO:probinson[2022-05-26];HPO:iea[2009-02-17];HPO:probinson[2022-05-25]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0003577	OMIM:615268	TAS					C	HPO:skoehler[2013-07-17]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0002540	PMID:22892528	PCS		1/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0002078	PMID:22892528	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0007371	PMID:22892528	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0001272	PMID:22892528	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0002120	PMID:22892528	PCS		4/4			P	HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0001260	PMID:22892528	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0000007	PMID:22892528	PCS					I	HPO:skoehler[2013-07-17];HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0009878	PMID:22892528	PCS					P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:615268	Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4		HP:0001249	PMID:22892528	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2023-04-09]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0000121	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0003411	PMID:25416932	PCS	HP:0003593	6/6			P	HPO:probinson[2015-03-08]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0003016	PMID:25416932	PCS					P	HPO:probinson[2015-03-08]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0004322	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0005871	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0003375	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002240	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001508	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002719	OMIM:260400	TAS					P	HPO:skoehler[2010-06-20]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001903	OMIM:260400	TAS					P	HPO:probinson[2012-07-28]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001328	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002812	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0006598	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0004979	PMID:25416932	PCS					P	HPO:probinson[2015-03-08]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0000774	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002910	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001700	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002750	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0003300	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002098	OMIM:260400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001263	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0011904	OMIM:260400	TAS					P	HPO:probinson[2012-07-28]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002570	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0000907	PMID:25416932	PCS	HP:0003593	6/6			P	HPO:probinson[2015-03-08]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001518	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001738	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0004808	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0006461	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0000007	OMIM:260400	TAS					I	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0000920	OMIM:260400	TAS					P	HPO:probinson[2012-07-28]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001873	OMIM:260400	TAS					P	HPO:probinson[2012-07-28]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001876	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002863	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0002643	OMIM:260400	TAS					P	HPO:probinson[2012-07-16]
OMIM:260400	Shwachman-Diamond syndrome 1		HP:0001875	OMIM:260400	TAS					P	HPO:probinson[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000486	PMID:29960046	PCS					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000046	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001250	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0002066	PMID:29960046	PCS					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0003593	PMID:12807966	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001290	PMID:12807966	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0002280	PMID:12807966	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000639	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0007065	PMID:12807966	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0011220	OMIM:300486	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000733	PMID:12807966	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0002119	PMID:12807966	PCS		4/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000219	OMIM:300486	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0025336	PMID:12807966	PCS		2/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0030260	OMIM:300486	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0006951	PMID:12807966	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000752	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000256	PMID:12807966	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001249	PMID:9582072;PMID:12807966	PCS		9/9			P	HPO:probinson[2021-09-25];HPO:skoehler[2010-06-20];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000336	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001320	PMID:12807966	PCS		4/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000054	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001344	PMID:12807966	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0003189	OMIM:300486	TAS					P	HPO:probinson[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000276	PMID:29960046	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0031936	PMID:12807966	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001321	PMID:12807966	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000490	PMID:12807966	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001263	PMID:29960046;PMID:12807966	PCS		15/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001419	PMID:9582072	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000448	PMID:12807966	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000744	PMID:12807966	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000601	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000400	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0002007	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0001257	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000322	OMIM:300486	PCS					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000303	PMID:12807966	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000028	OMIM:300486	IEA					P	HPO:iea[2009-02-17]
OMIM:300486	Intellectual developmental disorder, X-linked syndromic, Billuart type		HP:0000742	PMID:12807966	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:619452	Anencephaly 2		HP:0002323	PMID:32845958	PCS		3/3			P	HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0003577	PMID:32845958	PCS		3/3			C	HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0011803	PMID:32845958	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0000161	PMID:32845958	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0009099	PMID:32845958	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0000528	PMID:32845958	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0012745	PMID:32845958	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0000007	PMID:32845958	PCS					I	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:619452	Anencephaly 2		HP:0010289	PMID:32845958	PCS		1/2			P	HPO:probinson[2023-03-12]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0001561	PMID:12207937	PCS	HP:0011461	3/4			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0001181	PMID:12207937	PCS		1/5			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0003819	PMID:12207937	PCS		1/5			C	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0000239	PMID:12207937	PCS		1/5			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0000007	PMID:12207937	PCS					I	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0002804	PMID:12207937	PCS	HP:0003577	4/5			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0001558	PMID:12207937	PCS		5/5			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0002878	PMID:12207937	PCS		5/5			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0002304	PMID:12207937	PCS		5/5			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0003811	PMID:12207937	PCS		2/5			C	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0001522	PMID:12207937	PCS		2/5			C	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0000047	PMID:12207937	PCS					P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0003798	PMID:12207937	PCS		5/5			P	HPO:probinson[2021-06-26]
OMIM:619334	Arthrogryposis multiplex congenita 6		HP:0003557	PMID:12207937	PCS					P	HPO:probinson[2021-06-26]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002663	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001374	PMID:25130867	PCS		1/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000486	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0004322	PMID:28328135	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003311	PMID:25130867	PCS		1/3			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001371	OMIM:616007	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000160	PMID:25130867	PCS		1/3			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003196	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001252	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001097	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003593	PMID:25130867	PCS		3/3			C	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0011734	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000639	PMID:28328135	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000518	PMID:25130867;PMID:28328135	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0011220	PMID:25130867;PMID:28328135	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000238	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002936	PMID:25130867	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003307	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002857	PMID:25130867;PMID:28328135	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001763	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001265	OMIM:616007	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000574	PMID:25130867	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001382	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000490	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001263	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0011800	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001182	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0100585	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000407	PMID:25130867;PMID:28328135	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002827	PMID:28328135	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000007	PMID:25130867	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0008445	PMID:25130867	PCS		1/3			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000763	OMIM:616007	IEA					P	HPO:skoehler[2015-12-30]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000565	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003015	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002521	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003577	PMID:28328135	PCS		1/1			C	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000343	OMIM:616007	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000540	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001156	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002120	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001270	PMID:28328135	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0010306	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0007141	OMIM:616007	TAS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0007021	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000938	OMIM:616007	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001943	PMID:25130867	PCS		3/3			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001029	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001623	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002677	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003026	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000233	PMID:28328135	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002650	PMID:25130867	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000430	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002651	PMID:28328135	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003025	PMID:28328135	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0002571	PMID:25130867	PCS		1/3			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0005280	PMID:28328135	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0100876	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000508	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0009830	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000824	PMID:25130867	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003417	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0003416	OMIM:616007	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0001510	PMID:25130867	PCS		3/3			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000347	PMID:28328135	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000303	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0000666	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia		HP:0004425	OMIM:616007	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0002224	OMIM:610476	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0003621	PMID:17033975	PCS		1/7			C	HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0003596	PMID:17033975	PCS		4/7			C	HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0003584	PMID:17033975	PCS		1/7			C	HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0002094	PMID:17033975	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0011663	PMID:17033975	PCS					P	HPO:probinson[2013-03-11];HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0011462	PMID:17033975	PCS		1/7			C	HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0000007	OMIM:610476	TAS					I	HPO:skoehler[2012-10-17]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0004308	OMIM:610476	IEA					P	HPO:iea[2009-02-17]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0001962	PMID:17033975	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0001279	PMID:17033975	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0000982	OMIM:610476	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0000006	PMID:17033975	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610476	Arrhythmogenic right ventricular dysplasia, familial, 11		HP:0001645	PMID:17033975	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:193530	Weyers acrofacial dysostosis		HP:0000395	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0001792	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0004279	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0001156	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0001162	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0002164	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0000601	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0004209	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0001830	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0000006	OMIM:193530	IEA					I	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0006315	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0000698	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:193530	Weyers acrofacial dysostosis		HP:0003502	OMIM:193530	IEA					P	HPO:iea[2009-02-17]
OMIM:617319	Anterior segment dysgenesis 8		HP:0007957	PMID:27839872	IEA		0/4			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0009917	PMID:27839872	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0009918	PMID:27839872	PCS		4/4			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0012805	PMID:27839872	PCS		3/4			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0001083	PMID:27839872	PCS		3/3			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0001093	PMID:27839872	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0100693	PMID:27839872	PCS		3/4			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0012376	PMID:27839872	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0000518	PMID:27839872	PCS		4/4			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0012040	PMID:27839872	PCS		0/3			P	HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0011463	PMID:27839872	PCS					C	HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0000007	PMID:27839872	PCS					I	HPO:probinson[2017-06-16]
OMIM:617319	Anterior segment dysgenesis 8		HP:0007676	PMID:27839872	PCS		3/4			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:617319	Anterior segment dysgenesis 8		HP:0025358	PMID:27839872	PCS		3/4			P	HPO:probinson[2017-06-16];HPO:probinson[2024-03-15]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0002069	OMIM:604403	IEA					P	HPO:iea[2009-02-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0006813	OMIM:604403	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0002123	OMIM:604403	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0002373	OMIM:604403	IEA					P	HPO:iea[2009-02-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0011463	OMIM:604403	IEA					C	HPO:iea[2009-02-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0010819	OMIM:604403	IEA					P	HPO:iea[2009-02-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0002121	OMIM:604403	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0010818	OMIM:604403	IEA					P	HPO:iea[2009-02-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0003828	OMIM:604403	TAS					M	HPO:skoehler[2012-10-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0007359	OMIM:604403	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604403	Generalized epilepsy with febrile seizures plus, type 2		HP:0000006	OMIM:604403	IEA					I	HPO:iea[2009-02-17]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0002268	PMID:22120146	PCS		23/24			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0003621	PMID:22120146	PCS		22/24			C	HPO:probinson[2023-02-10]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0025708	PMID:22120146	PCS		2/24			C	HPO:probinson[2023-02-10]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0002197	OMIM:602066	IEA					P	HPO:iea[2009-02-17]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0007098	PMID:22120146	PCS		10/24			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0002372	OMIM:602066	IEA					P	HPO:iea[2009-02-17]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0012759	PMID:22120146	PCS		0/24			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-10]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0011157	PMID:22120146	PCS		10/24			P	HPO:probinson[2023-02-10]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0007359	OMIM:602066	IEA					P	HPO:iea[2009-02-17]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0000006	PMID:22120146	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:602066	Convulsions, familial infantile, with paroxysmal choreoathetosis		HP:0012469	PMID:22120146	PCS		4/24			P	HPO:probinson[2023-02-10]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000341	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000582	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0010804	PMID:33232677	PCS		2/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000343	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0001773	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000463	PMID:33232677	PCS		3/18			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0001250	PMID:33232677	PCS		3/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0001252	PMID:33232677	PCS		2/3			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000262	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0002162	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0001274	PMID:33232677	PCS		2/3			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0001251	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0025101	PMID:33232677	PCS		2/3			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0003593	PMID:33232677	PCS					C	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0010862	PMID:33232677	PCS		4/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0008070	PMID:33232677	PCS		2/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0045074	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0012469	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000718	PMID:33232677	PCS		2/5			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000954	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000414	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0002714	PMID:33232677	PCS		2/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000311	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0001249	PMID:33232677	PCS		9/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000215	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000358	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000297	PMID:33232677	PCS		1/3			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0002312	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000750	PMID:33232677	PCS		8/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000431	PMID:33232677	PCS		2/9			P	HPO:probinson[2021-07-01];HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0004279	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0005487	PMID:33232677	PCS		2/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0001263	PMID:33232677	PCS		8/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0045025	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0002194	PMID:33232677	PCS		6/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0010953	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000729	PMID:33232677	PCS		1/5			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000722	PMID:33232677	PCS		1/5			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0004209	PMID:33232677	PCS		3/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000400	PMID:33232677	PCS		2/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000664	PMID:33232677	PCS		2/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0007018	PMID:33232677	PCS		2/5			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000322	PMID:33232677	PCS		3/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000006	PMID:33232677	PCS					I	HPO:probinson[2021-07-01];HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000347	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000369	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:619320	Intellectual developmental disorder, autosomal dominant 65		HP:0000324	PMID:33232677	PCS		1/9			P	HPO:probinson[2021-07-01]
OMIM:600117	Dysphasia, familial developmental		HP:0002474	OMIM:600117	TAS					P	HPO:probinson[2012-07-24]
OMIM:600117	Dysphasia, familial developmental		HP:0002381	OMIM:600117	TAS					P	HPO:probinson[2009-02-17]
OMIM:600117	Dysphasia, familial developmental		HP:0000006	OMIM:600117	IEA					I	HPO:iea[2009-02-17]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0003621	PMID:9537424	PCS		2/2			C	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0003431	PMID:9537424	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0003376	OMIM:607678	IEA					P	HPO:iea[2009-02-17]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0003693	OMIM:607678	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0003484	OMIM:607678	IEA					P	HPO:probinson[2009-02-17]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0002460	PMID:9537424	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0009027	PMID:9537424	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0009830	PMID:9537424	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-27]
OMIM:607678	Charcot-Marie-Tooth disease, demyelinating, type 1D		HP:0000006	PMID:9537424	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0002783	PMID:33974130	PCS		1/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0000639	PMID:33974130	PCS		5/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0002110	PMID:33974130	PCS		1/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0000938	PMID:33974130	PCS		1/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0001263	PMID:33974130	PCS		3/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0001141	PMID:33974130	PCS	HP:0003621	8/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0000007	PMID:24726755	PCS					I	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0000543	PMID:33974130	PCS		5/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0002788	PMID:33974130	PCS		1/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0001522	PMID:33974130	PCS		2/10			C	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0002028	PMID:33974130	PCS	HP:0003623	10/10			P	HPO:probinson[2021-08-22]
OMIM:619446	Retinal dystrophy and microvillus inclusion disease		HP:0003623	PMID:33974130	PCS		10/10			C	HPO:probinson[2021-08-22]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000286	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000486	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000365	PMID:24810580	PCS		2/9			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0004322	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001252	PMID:24810580	PCS		5/10			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0012745	OMIM:612513	TAS					P	HPO:skoehler[2014-03-24]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0012110	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001848	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002539	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0008897	PMID:24810580	PCS		8/11			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0008734	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0003745	PMID:24810580	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001840	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000278	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001249	PMID:24810580	PCS		11/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001601	OMIM:612513	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000358	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002751	OMIM:612513	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000494	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000252	PMID:24810580	PCS		9/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000054	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002353	PMID:24810580	PCS		3/5			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001344	PMID:24810580	PCS		5/11			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002079	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0011968	PMID:24810580	PCS		7/8			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001263	PMID:24810580	PCS		11/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0012385	OMIM:612513	TAS					P	HPO:skoehler[2013-10-22]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000609	PMID:24810580	PCS		4/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000407	OMIM:612513	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000729	PMID:24810580	PCS		4/9			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000767	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002705	OMIM:612513	TAS					P	HPO:skoehler[2015-12-30]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000400	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002788	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001257	PMID:24810580	PCS		4/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000248	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000369	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000126	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001611	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000341	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000343	OMIM:612513	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000581	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0005274	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000219	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002119	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000218	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001302	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0006610	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000135	OMIM:612513	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001166	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0002059	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000431	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000232	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0005280	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0009473	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000506	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000508	OMIM:612513	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000505	PMID:24810580	PCS		6/9			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0001511	PMID:24810580	PCS		5/10			P	HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0007018	PMID:24810580	PCS		6/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-26]
OMIM:612513	Chromosome 2p16.1-p15 deletion syndrome		HP:0000028	OMIM:612513	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614162	Immunodeficiency 31C		HP:0002243	PMID:23534974	PCS		2/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0033608	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0004322	OMIM:614162	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0001890	PMID:23534974	PCS		1/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002240	PMID:23534974;PMID:23541320	PCS		4/10			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0032257	PMID:23541320	PCS		3/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0012203	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0012204	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0000819	OMIM:614162	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0032064	PMID:23534974	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002719	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0011463	PMID:23541320	PCS		1/5			C	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0000938	PMID:23534974	PCS		3/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002958	OMIM:614162	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0002716	PMID:23541320	PCS		2/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0001888	OMIM:614162	TAS				HP:0003676	P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0001945	PMID:23541320	PCS		2/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0001824	PMID:23541320	PCS		2/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0001324	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0003347	PMID:23534974	PCS		3/4			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0001744	PMID:23534974;PMID:23541320	PCS		4/10			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002754	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002014	OMIM:614162	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0003202	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002576	PMID:23534974	PCS		2/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0003621	PMID:23541320	PCS		2/5			C	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002110	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0012735	PMID:23541320	PCS		2/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0012378	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0032249	PMID:23541320	PCS		2/5			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0009098	PMID:23541320	PCS		1/5			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0025708	PMID:23541320	PCS		1/5			C	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0031382	PMID:23534974	PCS		2/2			P	HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002728	PMID:23541320	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0011473	PMID:23534974	PCS		3/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0000964	OMIM:614162	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0000821	OMIM:614162	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0000823	OMIM:614162	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0002205	PMID:23541320	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0001510	OMIM:614162	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614162	Immunodeficiency 31C		HP:0000006	PMID:21714643	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-11-07]
OMIM:614162	Immunodeficiency 31C		HP:0002721	PMID:23534974	PCS		5/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:153700	Macular dystrophy, vitelliform, 2		HP:0031526	OMIM:153700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:153700	Macular dystrophy, vitelliform, 2		HP:0007663	OMIM:153700	TAS					P	HPO:skoehler[2015-07-26]
OMIM:153700	Macular dystrophy, vitelliform, 2		HP:0000505	OMIM:153700	IEA					P	HPO:iea[2009-02-17]
OMIM:153700	Macular dystrophy, vitelliform, 2		HP:0008028	OMIM:153700	IEA					P	HPO:iea[2009-02-17]
OMIM:153700	Macular dystrophy, vitelliform, 2		HP:0007754	OMIM:153700	IEA					P	HPO:skoehler[2015-01-27]
OMIM:153700	Macular dystrophy, vitelliform, 2		HP:0000006	OMIM:153700	IEA					I	HPO:iea[2009-02-17]
OMIM:153700	Macular dystrophy, vitelliform, 2		HP:0000512	OMIM:153700	IEA					P	HPO:iea[2012-04-06]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0000132	PMID:28255014	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-20]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0001892	PMID:28255014	PCS		1/3			P	HPO:probinson[2022-10-20];HPO:probinson[2022-10-20]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0001596	OMIM:617443	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0003540	OMIM:617443	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0000007	OMIM:617443	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0000964	OMIM:617443	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0011877	PMID:28255014	PCS		3/3			P	HPO:probinson[2022-10-20]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0004429	OMIM:617443	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0001873	PMID:28255014;PMID:24100448	PCS		6/9		HP:0012825;HP:0012825	P	HPO:probinson[2022-10-20];HPO:skoehler[2018-10-08];HPO:probinson[2022-10-20]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0000006	PMID:24100448	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-20]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0003765	OMIM:617443	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617443	Bleeding disorder, platelet-type, 21		HP:0004866	PMID:28255014	PCS		2/2			P	HPO:probinson[2022-10-20]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0002059	PMID:31637422	PCS		4/4			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0000750	PMID:31637422	PCS		2/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0031936	PMID:31637422	PCS		5/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0002376	PMID:31637422	PCS		4/4			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0003487	PMID:31637422	PCS		5/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0025190	PMID:31637422	PCS	HP:0011463	4/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0000639	PMID:31637422	PCS		4/4			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0000007	PMID:31637422	PCS					I	HPO:probinson[2020-05-09];HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0007663	PMID:31637422	TAS		4/4			P	HPO:probinson[2020-05-09];HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0000648	PMID:31637422	PCS		1/4			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0025336	PMID:31637422	PCS	HP:0003593	3/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0007359	PMID:31637422	PCS	HP:0011463	2/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0001257	PMID:31637422	PCS		5/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0001249	PMID:31637422	PCS		5/5			P	HPO:probinson[2020-05-09]
OMIM:618770	Spastic paraplegia 82, autosomal recessive		HP:0001347	PMID:31637422	PCS		5/5			P	HPO:probinson[2020-05-09];HPO:probinson[2020-05-09]
OMIM:268060	Retinopathy, pericentral pigmentary, autosomal recessive		HP:0000483	OMIM:268060	TAS					P	HPO:probinson[2009-02-17]
OMIM:268060	Retinopathy, pericentral pigmentary, autosomal recessive		HP:0000486	OMIM:268060	TAS					P	HPO:probinson[2009-02-17]
OMIM:268060	Retinopathy, pericentral pigmentary, autosomal recessive		HP:0000540	OMIM:268060	TAS					P	HPO:probinson[2009-02-17]
OMIM:268060	Retinopathy, pericentral pigmentary, autosomal recessive		HP:0000580	OMIM:268060	TAS					P	HPO:probinson[2015-07-19]
OMIM:268060	Retinopathy, pericentral pigmentary, autosomal recessive		HP:0000007	OMIM:268060	TAS					I	HPO:probinson[2009-02-17]
OMIM:613625	Factor V and factor VIII, combined deficiency of		HP:0003125	PMID:18391077	PCS					P	HPO:probinson[2013-02-22];HPO:probinson[2020-07-20]
OMIM:613625	Factor V and factor VIII, combined deficiency of		HP:0000132	OMIM:613625	TAS					P	HPO:probinson[2013-02-22]
OMIM:613625	Factor V and factor VIII, combined deficiency of		HP:0003225	PMID:18391077	PCS					P	HPO:probinson[2013-02-22];HPO:probinson[2020-07-20]
OMIM:613625	Factor V and factor VIII, combined deficiency of		HP:0000007	PMID:18391077	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:613625	Factor V and factor VIII, combined deficiency of		HP:0001934	OMIM:613625	TAS					P	HPO:probinson[2013-02-22]
OMIM:613625	Factor V and factor VIII, combined deficiency of		HP:0000421	OMIM:613625	TAS					P	HPO:probinson[2013-02-22]
OMIM:601547	Cataract 3, multiple types		HP:0000519	OMIM:601547	IEA					P	HPO:skoehler[2015-01-27]
OMIM:601547	Cataract 3, multiple types		HP:0010698	OMIM:601547	IEA					P	HPO:skoehler[2019-02-22]
OMIM:601547	Cataract 3, multiple types		HP:0010695	PMID:11424921	PCS					P	HPO:skoehler[2014-05-24]
OMIM:601547	Cataract 3, multiple types		HP:0007976	OMIM:601547	TAS	HP:0003577	HP:0040280			P	HPO:skoehler[2013-01-09]
OMIM:601547	Cataract 3, multiple types		HP:0000006	PMID:11424921	PCS					I	HPO:skoehler[2013-01-11]
OMIM:600881	Cataract, congenital zonular, with sutural opacities		HP:0100018	PMID:9788845	PCS	HP:0003577	11/11			P	HPO:probinson[2022-11-06]
OMIM:600881	Cataract, congenital zonular, with sutural opacities		HP:0003577	PMID:9788845	PCS		11/11			C	HPO:probinson[2022-11-06]
OMIM:600881	Cataract, congenital zonular, with sutural opacities		HP:0008031	OMIM:600881	TAS					P	HPO:skoehler[2013-03-31]
OMIM:600881	Cataract, congenital zonular, with sutural opacities		HP:0000519	PMID:9788845	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-11-06]
OMIM:600881	Cataract, congenital zonular, with sutural opacities		HP:0000006	PMID:9788845	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-06]
OMIM:600881	Cataract, congenital zonular, with sutural opacities		HP:0010920	OMIM:600881	TAS					P	HPO:skoehler[2013-03-31]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002300	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0003676	OMIM:607136	IEA					C	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002067	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000640	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0003596	PMID:14985389	PCS		2/9			C	HPO:probinson[2022-07-01]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001310	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001332	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002186	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001272	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001250	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002066	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002063	OMIM:607136	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000020	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001251	PMID:14985389	PCS		12/15			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01];HPO:probinson[2021-06-25]
OMIM:607136	Spinocerebellar ataxia 17		HP:0011999	OMIM:607136	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002080	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000716	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000738	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000718	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0011462	PMID:14985389	PCS		6/9			C	HPO:probinson[2022-07-01]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000757	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0007668	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002136	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002015	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001289	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001300	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001260	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0003584	PMID:14985389	PCS		1/9			C	HPO:probinson[2022-07-01]
OMIM:607136	Spinocerebellar ataxia 17		HP:0003581	PMID:14985389	PCS		9/9			C	HPO:probinson[2021-06-25]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002072	PMID:14985389	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25];HPO:probinson[2022-07-01]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002171	OMIM:607136	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002070	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000727	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000726	PMID:14985389	PCS		5/5			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002506	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002529	OMIM:607136	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0002403	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000006	PMID:14985389	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:607136	Spinocerebellar ataxia 17		HP:0000743	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:607136	Spinocerebellar ataxia 17		HP:0001336	OMIM:607136	IEA					P	HPO:iea[2009-02-17]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0001155	PMID:28061825	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0000164	PMID:35996915	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0003577	PMID:12445216	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0001597	PMID:35996915	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0031528	PMID:35996915	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0000980	PMID:28061825	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0003593	PMID:28061825;PMID:11544476	PCS		12/12			C	HPO:probinson[2024-03-10];ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0032497	PMID:12445216	PCS					P	HP:probinson[2019-04-19]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0008070	PMID:11544476	PCS	HP:0003593	11/11			P	HPO:iea[2009-02-17];HP:probinson[2019-03-10];HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0008070	PMID:12445216	PCS	HP:0003593	4/4			P	HP:probinson[2019-06-12]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0008070	PMID:28061825	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0200040	PMID:28061825	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0011463	PMID:35996915	PCS		1/1			C	HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0000618	PMID:12445216	PCS	HP:0003581				P	HPO:iea[2009-02-17];HP:probinson[2019-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0007663	PMID:28061825;PMID:12445216;PMID:35996915	PCS		3/3			P	HPO:probinson[2024-03-10];ORCID:0000-0002-0736-9199[2024-05-22];HPO:skoehler[2015-07-26];HP:probinson[2019-03-10];HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0007401	PMID:28061825	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0007502	PMID:28061825	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0001760	PMID:28061825	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0410400	PMID:28061825	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0011509	PMID:28061825	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0006482	PMID:28061825	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0000608	PMID:11544476	PCS	HP:0003621	11/11			P	HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0002209	PMID:35996915	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0000007	PMID:12445216;PMID:11544476	PCS		20/20			I	HPO:iea[2009-02-17];HPO:probinson[2024-03-10];ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0030491	PMID:35996915	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0007754	PMID:12445216	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:601553	Hypotrichosis, congenital, with juvenile macular dystrophy		HP:0003777	PMID:28061825;PMID:12445216;PMID:11544476	PCS		12/12			P	HP:probinson[2019-06-12];HPO:iea[2009-02-17];HP:probinson[2019-03-10];ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003236	PMID:18195152	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003676	PMID:18195152	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003621	PMID:18195152	PCS		1/1			C	HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003551	OMIM:613157	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003560	PMID:18195152	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0001270	OMIM:613157	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003391	PMID:18195152	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0011003	PMID:18195152	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0012378	OMIM:613157	TAS					P	HPO:skoehler[2013-10-22]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0100297	PMID:18195152	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0008981	PMID:18195152	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0000007	PMID:18195152	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003307	PMID:18195152	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003712	OMIM:613157	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003701	PMID:18195152	PCS	HP:0003621	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:613157	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3		HP:0003557	PMID:18195152	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0000132	OMIM:605735	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0003577	OMIM:605735	TAS					C	HPO:skoehler[2012-10-17]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0002584	OMIM:605735	IEA					P	HPO:skoehler[2010-06-20]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0003540	OMIM:605735	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0000978	OMIM:605735	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0005261	OMIM:605735	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0000421	OMIM:605735	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605735	Bleeding disorder, platelet-type, 12		HP:0000006	OMIM:605735	IEA					I	HPO:skoehler[2010-06-19]
OMIM:607644	Candidiasis, familial, 3		HP:0008396	PMID:12205111	PCS					P	HPO:probinson[2019-04-20]
OMIM:607644	Candidiasis, familial, 3		HP:0000006	PMID:12205111	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2019-04-20]
OMIM:610338	Right pulmonary artery, anomalous origin of, familial		HP:0001629	OMIM:610338	IEA					P	HPO:iea[2009-02-17]
OMIM:610338	Right pulmonary artery, anomalous origin of, familial		HP:0001680	OMIM:610338	IEA					P	HPO:iea[2009-02-17]
OMIM:610338	Right pulmonary artery, anomalous origin of, familial		HP:0005143	OMIM:610338	IEA					P	HPO:iea[2009-02-17]
OMIM:610338	Right pulmonary artery, anomalous origin of, familial		HP:0001643	OMIM:610338	IEA					P	HPO:iea[2009-02-17]
OMIM:610338	Right pulmonary artery, anomalous origin of, familial		HP:0000006	OMIM:610338	IEA					I	HPO:iea[2009-02-17]
OMIM:610338	Right pulmonary artery, anomalous origin of, familial		HP:0001655	OMIM:610338	IEA					P	HPO:iea[2009-02-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001671	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0030853	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001696	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0004762	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001651	PMID:26437028	PCS		4/14			P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0004971	PMID:26437028	PCS		2/14			P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0011611	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0011565	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0005160	OMIM:616749	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0012020	PMID:26437028	PCS		1/14			P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0011671	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0011560	PMID:26437028	PCS		1/14			P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001702	PMID:26437028	PCS		1/14			P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001669	PMID:26437028	PCS		4/14			P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001646	PMID:26437028	PCS		1/14			P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0000007	PMID:26437028	PCS					I	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0006695	OMIM:616749	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001748	OMIM:616749	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0004935	OMIM:616749	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0000961	OMIM:616749	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0001631	PMID:26437028	PCS					P	HPO:probinson[2017-06-17]
OMIM:616749	Heterotaxy, visceral, 7, autosomal		HP:0002566	OMIM:616749	TAS					P	HPO:skoehler[2017-07-13]
OMIM:137245	Gastric lymphoma, primary		HP:0001442	OMIM:137245	TAS					I	HPO:probinson[2024-08-03]
OMIM:137245	Gastric lymphoma, primary		HP:0045038	PMID:8432445	PCS					P	HPO:skoehler[2015-08-22];HPO:probinson[2022-04-10]
OMIM:137245	Gastric lymphoma, primary		HP:0003581	PMID:8432445	PCS					C	HPO:probinson[2022-04-10]
OMIM:619491	Parkinson disease 24, autosomal dominant, susceptibility to		HP:0002322	PMID:32201884	PCS		4/6			P	HPO:probinson[2021-09-05]
OMIM:619491	Parkinson disease 24, autosomal dominant, susceptibility to		HP:0003596	PMID:32201884	PCS		5/6			C	HPO:probinson[2021-09-05]
OMIM:619491	Parkinson disease 24, autosomal dominant, susceptibility to		HP:0000716	PMID:32201884	PCS		2/6			P	HPO:probinson[2021-09-05]
OMIM:619491	Parkinson disease 24, autosomal dominant, susceptibility to		HP:0011462	PMID:32201884	PCS		1/6			C	HPO:probinson[2021-09-05]
OMIM:619491	Parkinson disease 24, autosomal dominant, susceptibility to		HP:0002063	PMID:32201884	PCS		1/6			P	HPO:probinson[2021-09-05]
OMIM:619491	Parkinson disease 24, autosomal dominant, susceptibility to		HP:0002548	PMID:32201884	PCS		6/6			P	HPO:probinson[2021-09-05]
OMIM:619491	Parkinson disease 24, autosomal dominant, susceptibility to		HP:0000006	PMID:32201884	PCS					I	HPO:probinson[2021-09-05];HPO:probinson[2021-09-05]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0002188	PMID:36608681	PCS		4/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0004322	PMID:36608681	PCS		2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001250	PMID:36608681	PCS		3/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001252	PMID:36608681	PCS	HP:0003593	3/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001373	PMID:36608681	PCS		2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0002240	PMID:36608681	PCS	HP:0003593	2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0002180	PMID:36608681	PCS		4/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001629	PMID:36608681	PCS		1/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001888	PMID:36608681	PCS		3/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0008897	PMID:36608681	PCS		2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0002119	PMID:36608681	PCS		3/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001744	PMID:36608681	PCS	HP:0003593	3/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0004315	PMID:36608681	PCS		2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0002850	PMID:36608681	PCS		1/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0000175	PMID:36608681	PCS		1/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0000010	PMID:36608681	PCS		2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0002079	PMID:36608681	PCS		4/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001387	PMID:36608681	PCS		1/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001882	PMID:36608681	PCS		3/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001382	PMID:36608681	PCS		2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001263	PMID:36608681	PCS		4/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001680	PMID:36608681	PCS		1/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0001581	PMID:36608681	PCS		2/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0000007	PMID:36608681	PCS					I	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0002205	PMID:36608681	PCS		4/4			P	HPO:probinson[2023-04-16]
OMIM:620210	Neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia		HP:0004349	PMID:36608681	PCS		4/4			P	HPO:probinson[2023-04-16]
OMIM:183086	Spinocerebellar ataxia 6		HP:0007979	PMID:9345107	PCS		3/5			P	HPO:probinson[2023-01-30];HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0003676	PMID:9345107	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0001310	PMID:9345107	PCS		1/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002321	PMID:9345107	PCS		2/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0001272	PMID:9345107	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002120	PMID:9345107	PCS		1/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0001251	PMID:9345107	PCS		4/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0001350	PMID:9345107	PCS		4/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002083	PMID:9345107	PCS		2/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002080	PMID:9345107	PCS		1/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0000639	PMID:9345107	PCS		1/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0011462	PMID:9345107	PCS		1/5			C	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002359	PMID:9345107	PCS		1/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0003743	OMIM:183086	IEA					I	HPO:iea[2009-02-17]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002017	PMID:9345107	PCS		2/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002311	PMID:9345107	PCS		2/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0003587	PMID:9345107	PCS		1/5			C	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002015	OMIM:183086	IEA					P	HPO:iea[2009-02-17]
OMIM:183086	Spinocerebellar ataxia 6		HP:0003621	PMID:9345107	PCS		4/5			C	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002078	PMID:9345107	PCS		1/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0001260	OMIM:183086	IEA					P	HPO:iea[2009-02-17]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002073	PMID:9345107	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0007670	OMIM:183086	IEA					P	HPO:iea[2009-02-17]
OMIM:183086	Spinocerebellar ataxia 6		HP:0007772	OMIM:183086	IEA					P	HPO:skoehler[2010-06-18]
OMIM:183086	Spinocerebellar ataxia 6		HP:0002505	PMID:9345107	PCS		1/5			P	HPO:probinson[2023-01-30]
OMIM:183086	Spinocerebellar ataxia 6		HP:0000763	OMIM:183086	IEA					P	HPO:iea[2009-02-17]
OMIM:183086	Spinocerebellar ataxia 6		HP:0000006	PMID:8988170	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:250500	Metaphyseal modeling abnormality, skin lesions, and spastic paraplegia		HP:0011001	OMIM:250500	IEA					P	HPO:iea[2009-02-17]
OMIM:250500	Metaphyseal modeling abnormality, skin lesions, and spastic paraplegia		HP:0000007	OMIM:250500	IEA					I	HPO:iea[2009-02-17]
OMIM:250500	Metaphyseal modeling abnormality, skin lesions, and spastic paraplegia		HP:0001258	OMIM:250500	IEA					P	HPO:iea[2009-02-17]
OMIM:250500	Metaphyseal modeling abnormality, skin lesions, and spastic paraplegia		HP:0000951	OMIM:250500	IEA					P	HPO:iea[2009-02-17]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0003577	PMID:12189163	PCS		1/1			C	HPO:probinson[2022-09-02]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001058	PMID:22829427	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000023	PMID:22829427	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001252	PMID:22829427	PCS		1/2			P	HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0004381	PMID:12189163;PMID:22829427	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0025082	PMID:12189163	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001548	OMIM:219100	TAS					P	HPO:skoehler[2014-11-26]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000015	PMID:12189163	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000776	PMID:22829427	PCS	HP:0003577	0/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000974	PMID:22829427	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000973	PMID:12189163;PMID:22829427	PCS		6/6			P	HPO:probinson[2022-09-02];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001166	OMIM:219100	TAS					P	HPO:skoehler[2014-11-26]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001562	OMIM:219100	IEA					P	HPO:iea[2009-02-17]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000252	OMIM:219100	TAS					P	HPO:skoehler[2014-11-26]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0004970	OMIM:219100	IEA					P	HPO:iea[2009-02-17]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001382	OMIM:219100	IEA					P	HPO:iea[2009-02-17]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001582	PMID:12189163	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0002097	PMID:12189163;PMID:22829427	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0034273	PMID:22829427	PCS		1/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000767	OMIM:219100	IEA					P	HPO:iea[2009-02-17]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001537	OMIM:219100	IEA					P	HPO:iea[2009-02-17]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0000007	PMID:12189163	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0004948	OMIM:219100	IEA					P	HPO:iea[2009-02-17]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0004969	PMID:22829427	PCS		1/2			P	HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0001659	PMID:22829427	PCS		1/2			P	HPO:probinson[2024-03-08]
OMIM:219100	Cutis laxa, autosomal recessive, type IA		HP:0002205	PMID:12189163	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:620576	Otosclerosis 11		HP:0008529	PMID:34633540	PCS					P	HPO:probinson[2024-03-12]
OMIM:620576	Otosclerosis 11		HP:0000362	PMID:34633540	PCS					P	HPO:probinson[2024-03-12]
OMIM:620576	Otosclerosis 11		HP:0003621	PMID:34633540	PCS		2/8			C	HPO:probinson[2024-03-12]
OMIM:620576	Otosclerosis 11		HP:0000407	PMID:34633540	PCS		4/8			P	HPO:probinson[2024-03-12]
OMIM:620576	Otosclerosis 11		HP:0011462	PMID:34633540	PCS		6/8			C	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620576	Otosclerosis 11		HP:0000405	PMID:34633540	PCS		5/8			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620576	Otosclerosis 11		HP:0000006	PMID:34633540	PCS					I	HPO:probinson[2024-03-12]
OMIM:300323	Gout, hprt-related		HP:0000083	OMIM:300323	TAS					P	HPO:probinson[2009-02-17]
OMIM:300323	Gout, hprt-related		HP:0001419	OMIM:300323	TAS					I	HPO:probinson[2009-02-17]
OMIM:300323	Gout, hprt-related		HP:0000787	OMIM:300323	TAS					P	HPO:probinson[2009-02-17]
OMIM:300323	Gout, hprt-related		HP:0001854	OMIM:300323	TAS					P	HPO:probinson[2009-02-17]
OMIM:300323	Gout, hprt-related		HP:0003149	OMIM:300323	TAS					P	HPO:probinson[2009-02-17]
OMIM:300323	Gout, hprt-related		HP:0002149	OMIM:300323	TAS					P	HPO:probinson[2012-07-19]
OMIM:254000	Muscular dystrophy, congenital, with infantile cataract and hypogonadism		HP:0000518	OMIM:254000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254000	Muscular dystrophy, congenital, with infantile cataract and hypogonadism		HP:0003560	OMIM:254000	IEA					P	HPO:iea[2009-02-17]
OMIM:254000	Muscular dystrophy, congenital, with infantile cataract and hypogonadism		HP:0000007	OMIM:254000	IEA					I	HPO:iea[2009-02-17]
OMIM:254000	Muscular dystrophy, congenital, with infantile cataract and hypogonadism		HP:0000135	OMIM:254000	IEA					P	HPO:iea[2009-02-17]
OMIM:167300	Paget disease, extramammary		HP:0002664	OMIM:167300	IEA					P	HPO:iea[2009-02-17]
OMIM:167300	Paget disease, extramammary		HP:0000964	OMIM:167300	TAS					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000286	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000252	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0002059	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000486	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0002650	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0001442	OMIM:300337	IEA					I	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0001596	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0001250	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0001161	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0005593	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0002282	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000280	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000518	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0002808	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000316	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0009466	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000612	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0030084	OMIM:300337	TAS					P	HPO:skoehler[2014-09-21]
OMIM:300337	Hypomelanosis of Ito		HP:0001159	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000179	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0000256	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0001249	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:300337	Hypomelanosis of Ito		HP:0006316	OMIM:300337	IEA					P	HPO:iea[2009-02-17]
OMIM:301029	Shukla-Vernon syndrome		HP:0000486	PMID:30941876	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0001272	PMID:30941876	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0001250	PMID:24123876;PMID:30941876	PCS		3/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0001252	PMID:24123876;PMID:30941876	PCS		4/7			P	HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0003593	PMID:30941876	PCS		5/5			C	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000280	PMID:24123876	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0008070	PMID:30941876	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000718	PMID:30941876	PCS		2/5			P	HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000316	PMID:30941876	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0100807	PMID:30941876	PCS		3/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000733	PMID:30941876	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000577	PMID:30941876	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0002136	PMID:30941876	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000494	PMID:30941876	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000750	PMID:30941876	PCS		3/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000276	PMID:30941876	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0001263	PMID:30941876	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0002194	PMID:30941876	PCS		4/5			P	HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0001182	OMIM:301029	IEA					P	HPO:skoehler[2019-09-07]
OMIM:301029	Shukla-Vernon syndrome		HP:0012810	PMID:30941876	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0100710	PMID:30941876	PCS		2/5			P	HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0001419	PMID:24123876	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000729	PMID:30941876	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000767	PMID:30941876	PCS		1/5			P	HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0000348	PMID:30941876	PCS		4/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0002307	PMID:30941876	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:301029	Shukla-Vernon syndrome		HP:0007018	PMID:30941876	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-26]
OMIM:163600	Nipples inverted		HP:0003186	OMIM:163600	IEA					P	HPO:iea[2009-02-17]
OMIM:163600	Nipples inverted		HP:0000006	OMIM:163600	IEA					I	HPO:iea[2009-02-17]
OMIM:615297	Adams-Oliver syndrome 4		HP:0003577	PMID:23522784	PCS		5/5			C	HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0001057	PMID:23522784	PCS		5/5			P	HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0100381	PMID:23522784	PCS		1/5			P	HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0100382	PMID:23522784	PCS		1/5			P	HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0010645	PMID:23522784	PCS		2/5			P	HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0100797	PMID:23522784	PCS		2/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0001629	PMID:23522784	PCS		1/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0000965	PMID:23522784	PCS		1/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0001537	PMID:23522784	PCS		2/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0000007	PMID:23522784	PCS					I	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0001800	PMID:23522784	PCS		2/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0000568	PMID:23522784	PCS		0/5			P	HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0001643	PMID:23522784	PCS		1/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0001631	PMID:23522784	PCS		1/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:615297	Adams-Oliver syndrome 4		HP:0001831	PMID:23522784	PCS		1/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-30]
OMIM:166750	Otodental dysplasia		HP:0000343	OMIM:166750	IEA					P	HPO:skoehler[2010-06-18]
OMIM:166750	Otodental dysplasia		HP:0000684	PMID:17656375	IEA					P	HPO:probinson[2022-03-23]
OMIM:166750	Otodental dysplasia		HP:0011051	PMID:17656375	PCS					P	HPO:probinson[2022-03-23]
OMIM:166750	Otodental dysplasia		HP:0000276	OMIM:166750	IEA					P	HPO:skoehler[2010-06-18]
OMIM:166750	Otodental dysplasia		HP:0000463	OMIM:166750	IEA					P	HPO:skoehler[2010-06-18]
OMIM:166750	Otodental dysplasia		HP:0000407	OMIM:166750	IEA					P	HPO:iea[2009-02-17]
OMIM:166750	Otodental dysplasia		HP:0003771	PMID:17656375	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-23]
OMIM:166750	Otodental dysplasia		HP:0033791	PMID:17656375	PCS					P	HPO:probinson[2022-03-23]
OMIM:166750	Otodental dysplasia		HP:0006297	PMID:17656375	PCS					P	HPO:probinson[2022-03-23]
OMIM:166750	Otodental dysplasia		HP:0000679	OMIM:166750	IEA					P	HPO:iea[2009-02-17]
OMIM:166750	Otodental dysplasia		HP:0000006	PMID:17656375	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:166750	Otodental dysplasia		HP:0000589	OMIM:166750	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:617480	46,xx sex reversal 4		HP:0000808	PMID:27378692	PCS	HP:0003577	1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0000054	PMID:27378692	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0012861	PMID:27378692	PCS		2/4			P	HPO:probinson[2023-02-26];HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0000133	PMID:27378692	PCS					P	HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0000062	PMID:27378692	PCS	HP:0003577	2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0003829	OMIM:617480	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617480	46,xx sex reversal 4		HP:0025486	PMID:27378692	PCS		1/6			P	HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0012646	PMID:27378692	PCS		1/6			P	HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0008665	PMID:27378692	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-26]
OMIM:617480	46,xx sex reversal 4		HP:0000006	PMID:27378692	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-26]
OMIM:616946	Premature ovarian failure 11		HP:0000869	PMID:26218421	PCS		6/6			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-15]
OMIM:616946	Premature ovarian failure 11		HP:0011462	PMID:26218421	PCS		6/6			C	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:616946	Premature ovarian failure 11		HP:0008232	PMID:26218421	PCS					P	HPO:probinson[2017-06-23]
OMIM:616946	Premature ovarian failure 11		HP:0000876	PMID:26218421	PCS					P	HPO:probinson[2017-06-23]
OMIM:616946	Premature ovarian failure 11		HP:0000006	PMID:26218421	PCS					I	HPO:probinson[2017-06-23]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000939	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000716	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0012030	PMID:12213893	PCS		5/5			P	HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000938	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0011462	PMID:12213893	PCS		1/5			C	HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000739	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000712	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000978	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000713	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000311	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0001268	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0003466	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0003621	PMID:12213893	PCS		4/5			C	HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0001580	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0001065	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0030088	PMID:12213893	PCS		2/4			P	HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0031214	PMID:12213893	PCS		3/4			P	HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000709	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0002808	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000869	PMID:12213893	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000822	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0001956	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0003118	PMID:12213893	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0002920	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000006	PMID:12213893	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0000963	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:610489	Pigmented nodular adrenocortical disease, primary, 1		HP:0001579	OMIM:610489	IEA					P	HPO:iea[2009-02-17]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000044	PMID:14573733	PCS		6/6			P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-19]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000054	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0003621	PMID:14573733	PCS		6/6			C	HPO:probinson[2023-01-19]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000013	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0002750	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000771	OMIM:614837	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0030344	PMID:14573733	PCS		6/6			P	HPO:probinson[2023-01-19]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0030341	PMID:14573733	PCS		6/6			P	HPO:probinson[2023-01-19]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0008197	PMID:14573733	PCS		6/6			P	HPO:probinson[2023-01-19]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000938	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000458	OMIM:614837	IEA		HP:0040283			P	HPO:probinson[2013-08-10]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000007	PMID:14573733	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-01-19]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0008734	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000028	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000027	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614837	Hypogonadotropic hypogonadism 8 with or without anosmia		HP:0000786	OMIM:614837	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614823	Aortic valve disease 2		HP:0004963	PMID:22275001	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0001650	PMID:30796334;PMID:22275001	PCS		5/22			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0003577	PMID:22275001	PCS		1/1			C	HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0001680	PMID:22275001	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:4000158	PMID:30796334	PCS					I	HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0001647	PMID:30796334;PMID:22275001	PCS		9/22			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0001659	PMID:30796334	PCS		4/20			P	HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0006687	PMID:30796334	PCS		1/20			P	HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0001653	PMID:30796334	PCS		4/40			P	HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0001642	PMID:30796334	PCS		1/20			P	HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0004933	PMID:30796334	PCS		2/20			P	HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0000006	PMID:22275001	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0004942	PMID:30796334	PCS		5/20			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-07]
OMIM:614823	Aortic valve disease 2		HP:0001655	PMID:30796334	PCS		2/20			P	HPO:probinson[2023-02-07]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0002366	PMID:20110243	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0003621	PMID:20110243	PCS		10/23			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0003487	PMID:20110243	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0003693	PMID:20110243	PCS		23/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0002483	PMID:20110243	PCS		15/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0001260	PMID:20110243	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0000020	PMID:20110243	PCS		1/23			P	HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0002460	PMID:20110243	PCS		23/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0002380	PMID:20110243	PCS		15/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0033725	PMID:20110243	PCS		0/23			P	HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0100543	PMID:20110243	PCS		0/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0011462	PMID:20110243	PCS		13/23			C	HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0007354	PMID:20110243	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0000007	PMID:20110243	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0007256	PMID:20110243	PCS		23/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0002747	PMID:20110243	PCS		2/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0001257	PMID:20110243	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0003677	PMID:20110243	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0002500	PMID:20110243	PCS		0/23			P	HPO:probinson[2022-09-25]
OMIM:602099	Amyotrophic lateral sclerosis 5, juvenile		HP:0001347	PMID:20110243	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-25]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001355	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001250	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001090	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001629	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0000618	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001548	PMID:22729224	PCS		2/11			P	HPO:probinson[2022-10-18]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0000238	PMID:22729224	PCS		13/13			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-10-18]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0000637	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0002119	PMID:22729224	PCS		13/13			P	HPO:probinson[2022-10-18]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001302	OMIM:603387	TAS					P	HPO:skoehler[2012-12-06]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0000256	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0008936	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0003202	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0025352	PMID:22729224	PCS					I	HPO:probinson[2022-10-18]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0002079	OMIM:603387	TAS					P	HPO:skoehler[2012-12-06]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001263	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0010775	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0100259	PMID:22729224	PCS	HP:0003577	2/13			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-10-18]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0006380	OMIM:603387	TAS					P	HPO:skoehler[2012-12-06]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0007074	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0002808	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0000508	OMIM:603387	TAS					P	HPO:skoehler[2012-12-06]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0002007	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001631	OMIM:603387	TAS					P	HPO:skoehler[2012-12-02]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0001653	OMIM:603387	TAS					P	HPO:skoehler[2012-12-06]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0002943	OMIM:603387	TAS					P	HPO:skoehler[2012-12-06]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0000006	PMID:22729224	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2022-10-18]
OMIM:603387	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome		HP:0002126	PMID:22729224	PCS		13/13			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-10-18]
OMIM:613194	Retinitis pigmentosa-50		HP:0012045	PMID:19853238	PCS					P	HPO:probinson[2013-06-02]
OMIM:613194	Retinitis pigmentosa-50		HP:0000662	PMID:19853238	PCS					P	HPO:probinson[2013-06-02]
OMIM:613194	Retinitis pigmentosa-50		HP:0000541	PMID:19853238	PCS					P	HPO:probinson[2013-06-02]
OMIM:613194	Retinitis pigmentosa-50		HP:0007663	PMID:19853238	PCS	HP:0003621				P	HPO:probinson[2013-06-02]
OMIM:613194	Retinitis pigmentosa-50		HP:0000543	PMID:19853238	PCS					P	HPO:probinson[2013-06-02]
OMIM:613194	Retinitis pigmentosa-50		HP:0000510	OMIM:613194	IEA					P	HPO:skoehler[2015-01-19]
OMIM:613194	Retinitis pigmentosa-50		HP:0007843	PMID:19853238	PCS					P	HPO:probinson[2013-06-02]
OMIM:613194	Retinitis pigmentosa-50		HP:0000006	PMID:19853238	PCS					I	HPO:probinson[2013-06-02]
OMIM:613194	Retinitis pigmentosa-50		HP:0000512	PMID:19853238	PCS					P	HPO:probinson[2013-06-02]
OMIM:301015	Hemolytic anemia, congenital, X-linked		HP:0003577	PMID:26944472	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-30]
OMIM:301015	Hemolytic anemia, congenital, X-linked		HP:0001419	PMID:26944472	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-30]
OMIM:301015	Hemolytic anemia, congenital, X-linked		HP:0001878	PMID:26944472	PCS		1/1		HP:0012825	P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-30]
OMIM:301015	Hemolytic anemia, congenital, X-linked		HP:0040319	PMID:26944472	PCS	HP:0011463	1/1			P	HPO:probinson[2021-10-30]
OMIM:301015	Hemolytic anemia, congenital, X-linked		HP:0000952	PMID:26944472	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-30]
OMIM:611783	Erythrocytosis, familial, 4		HP:0030248	PMID:18378852	PCS		1/5			P	HPO:probinson[2021-02-19]
OMIM:611783	Erythrocytosis, familial, 4		HP:0011462	PMID:18378852;PMID:18184961	PCS		6/6			C	HPO:probinson[2020-07-20];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:611783	Erythrocytosis, familial, 4		HP:0001900	PMID:18378852;PMID:18184961	PCS		6/6			P	HPO:probinson[2013-04-02];HPO:probinson[2020-07-20];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:611783	Erythrocytosis, familial, 4		HP:0001899	PMID:18378852;PMID:18184961	PCS		5/5			P	HPO:probinson[2013-04-02];HPO:probinson[2020-07-20];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:611783	Erythrocytosis, familial, 4		HP:0002625	PMID:18184961	PCS	HP:0003596	1/1			P	HPO:probinson[2021-02-19]
OMIM:611783	Erythrocytosis, familial, 4		HP:0000989	PMID:18378852	PCS		2/5			P	HPO:probinson[2021-02-19]
OMIM:611783	Erythrocytosis, familial, 4		HP:0033644	PMID:18378852;PMID:18184961	PCS		6/6			P	HPO:probinson[2021-04-16]
OMIM:611783	Erythrocytosis, familial, 4		HP:0001901	PMID:18184961	PCS		1/1			P	HPO:probinson[2013-04-02];HPO:probinson[2020-07-20];HPO:probinson[2021-02-19]
OMIM:611783	Erythrocytosis, familial, 4		HP:0000006	PMID:18184961	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:222800	Erythrocytosis, familial, 8		HP:0003581	PMID:15054810	PCS		1/1			C	HPO:probinson[2022-11-01]
OMIM:222800	Erythrocytosis, familial, 8		HP:0001900	PMID:15054810	PCS		1/1			P	HPO:probinson[2022-11-01]
OMIM:222800	Erythrocytosis, familial, 8		HP:6000557	PMID:25015942	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:222800	Erythrocytosis, familial, 8		HP:0000007	PMID:2542247	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-01]
OMIM:222800	Erythrocytosis, familial, 8		HP:0001899	PMID:15054810	PCS		1/1			P	HPO:probinson[2022-11-01]
OMIM:222800	Erythrocytosis, familial, 8		HP:0001901	PMID:15054810;PMID:2542247	PCS		2/2			P	HPO:probinson[2022-11-01];HPO:skoehler[2019-02-22];HPO:probinson[2022-11-01]
OMIM:222800	Erythrocytosis, familial, 8		HP:0001744	PMID:15054810	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-01]
OMIM:620238	Deafness, autosomal recessive 120		HP:0003577	PMID:35727972	PCS		11/11			C	HPO:probinson[2023-06-12]
OMIM:620238	Deafness, autosomal recessive 120		HP:0000407	PMID:35727972	PCS		11/11			P	HPO:probinson[2023-06-12]
OMIM:620238	Deafness, autosomal recessive 120		HP:0000007	PMID:35727972	PCS					I	HPO:probinson[2023-06-12]
OMIM:218550	Craniosynostosis with fibular aplasia		HP:0001363	PMID:8100584	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:218550	Craniosynostosis with fibular aplasia		HP:0002990	PMID:8100584	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:218550	Craniosynostosis with fibular aplasia		HP:0000954	PMID:8100584	PCS		2/2		HP:0012832	P	HPO:probinson[2018-06-13]
OMIM:218550	Craniosynostosis with fibular aplasia		HP:0000007	PMID:8100584	PCS					I	HPO:iea[2009-02-17]
OMIM:218550	Craniosynostosis with fibular aplasia		HP:0000028	PMID:8100584	PCS		2/2			P	HPO:probinson[2018-06-13]
OMIM:155601	Melanoma, cutaneous malignant, susceptibility to, 2		HP:0012056	OMIM:155601	TAS					P	HPO:probinson[2009-02-17]
OMIM:155601	Melanoma, cutaneous malignant, susceptibility to, 2		HP:0000006	OMIM:155601	TAS					I	HPO:probinson[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0000175	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0000252	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0007968	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0004322	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0000007	OMIM:257910	IEA					I	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0000568	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0001257	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0001249	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:257910	Oculopalatocerebral syndrome		HP:0000555	OMIM:257910	IEA					P	HPO:iea[2009-02-17]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001254	PMID:11220739	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001252	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001251	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0003593	PMID:11220739	PCS		4/6			C	HPO:skoehler[2019-02-15]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001290	PMID:11220739	PCS		2/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001270	PMID:11220739	PCS		3/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0012444	PMID:11220739	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001508	PMID:11220739	PCS		4/6			P	HPO:skoehler[2019-04-18]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0000639	PMID:11220739	PCS		3/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0002119	PMID:11220739	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001942	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001347	PMID:11220739	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0003128	PMID:11220739	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0003623	PMID:11220739	PCS		2/6			C	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0008936	PMID:11220739	PCS		2/6			P	HPO:skoehler[2019-02-15]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0003202	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0002376	PMID:11220739	PCS		1/6			P	HPO:skoehler[2019-02-15]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0002013	PMID:11220739	PCS		3/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001263	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0002151	PMID:11220739	PCS		3/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0011923	PMID:11220739	PCS		6/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0002093	PMID:11220739	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0010535	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001639	PMID:11220739	PCS		2/6			P	HPO:skoehler[2019-04-18]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0007256	PMID:11220739	PCS		1/6			P	HPO:skoehler[2019-02-15]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0000007	PMID:11220739	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0001712	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0000648	PMID:11220739	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0000543	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0004900	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0002104	PMID:11220739	PCS		1/6			P	HPO:probinson[2023-06-05]
OMIM:618228	Mitochondrial complex I deficiency, nuclear type 6		HP:0000666	PMID:11220739	PCS		2/6			P	HPO:probinson[2023-06-05]
OMIM:600467	Malignant hyperthermia, susceptibility to, 4		HP:0002047	OMIM:600467	IEA					P	HPO:iea[2009-02-17]
OMIM:600467	Malignant hyperthermia, susceptibility to, 4		HP:0003201	OMIM:600467	IEA					P	HPO:iea[2009-02-17]
OMIM:600467	Malignant hyperthermia, susceptibility to, 4		HP:0000006	OMIM:600467	IEA					I	HPO:iea[2009-02-17]
OMIM:600467	Malignant hyperthermia, susceptibility to, 4		HP:0001941	OMIM:600467	IEA					P	HPO:iea[2009-02-17]
OMIM:125480	Major affective disorder 1		HP:0100754	OMIM:125480	TAS					P	HPO:probinson[2013-12-18]
OMIM:125480	Major affective disorder 1		HP:0000716	OMIM:125480	TAS					P	HPO:probinson[2009-02-17]
OMIM:125480	Major affective disorder 1		HP:0000006	OMIM:125480	TAS					I	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0002025	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0011917	OMIM:181450	TAS					P	HPO:probinson[2012-06-08]
OMIM:181450	Ulnar-Mammary syndrome		HP:0003577	PMID:12116211	PCS		2/3			C	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0002023	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0010627	OMIM:181450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000882	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000046	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000023	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0002021	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0030011	OMIM:181450	TAS					P	HPO:skoehler[2014-09-21]
OMIM:181450	Ulnar-Mammary syndrome		HP:0005792	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0011755	OMIM:181450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0011675	OMIM:181450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:181450	Ulnar-Mammary syndrome		HP:0010046	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0009281	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0008093	OMIM:181450	TAS					P	HPO:probinson[2012-06-08]
OMIM:181450	Ulnar-Mammary syndrome		HP:0009460	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0001607	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0001629	OMIM:181450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0011462	PMID:12116211	PCS		1/3			C	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000813	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0025259	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0002557	PMID:12116211	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000894	OMIM:181450	TAS					P	HPO:probinson[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0002215	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000054	PMID:12116211	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0003982	PMID:12116211	PCS		1/3			P	HPO:probinson[2012-06-08];HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0003187	PMID:12116211	PCS		1/1	FEMALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0003022	OMIM:181450	TAS					P	HPO:probinson[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0001162	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0003186	OMIM:181450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0010040	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0010043	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0007397	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000668	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0009238	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000823	PMID:12116211	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0009237	PMID:12116211	PCS		2/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0003977	OMIM:181450	TAS					P	HPO:probinson[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0002987	PMID:12116211	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0003974	OMIM:181450	TAS					P	HPO:probinson[2012-06-08]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000006	PMID:9207801	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:181450	Ulnar-Mammary syndrome		HP:0002984	OMIM:181450	TAS					P	HPO:probinson[2012-06-08]
OMIM:181450	Ulnar-Mammary syndrome		HP:0001513	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0000049	OMIM:181450	IEA					P	HPO:iea[2009-02-17]
OMIM:181450	Ulnar-Mammary syndrome		HP:0005338	OMIM:181450	TAS					P	HPO:probinson[2012-06-08]
OMIM:604173	Poikiloderma with neutropenia		HP:0003236	PMID:20734427;PMID:20004881	PCS		5/6			P	HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000343	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0004322	PMID:20734427;PMID:20004881	PCS		4/6			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0002162	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0003196	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0003593	PMID:20734427;PMID:20004881;PMID:20503306	PCS		9/9			C	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0045075	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000316	PMID:20734427	PCS		2/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0001009	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000579	PMID:20503306	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0025435	PMID:20734427;PMID:20004881	PCS		5/6			P	HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0006532	PMID:20734427;PMID:20004881	PCS		4/6			P	HPO:skoehler[2012-11-21];HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0007588	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000498	OMIM:604173	TAS					P	HPO:skoehler[2013-05-29]
OMIM:604173	Poikiloderma with neutropenia		HP:0000278	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0001029	PMID:20734427;PMID:20004881;PMID:20503306	PCS		9/9			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0001744	PMID:20734427;PMID:20004881	PCS		5/6			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000670	PMID:20503306	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0006538	PMID:20503306	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0004334	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0001387	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0001882	PMID:20734427	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000430	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0001382	PMID:20734427	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0011800	PMID:20734427;PMID:20004881	PCS		5/6			P	HPO:skoehler[2013-11-28];HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0005280	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0011108	PMID:20734427;PMID:20004881	PCS		4/6			P	HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000969	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000509	OMIM:604173	TAS					P	HPO:skoehler[2013-05-29]
OMIM:604173	Poikiloderma with neutropenia		HP:0000007	PMID:20004881	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-03-10]
OMIM:604173	Poikiloderma with neutropenia		HP:0000403	PMID:20734427;PMID:20004881	PCS		4/6			P	HPO:skoehler[2012-11-21];HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000988	PMID:20734427	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0002007	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0008404	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0007556	PMID:20004881	PCS		3/3			P	HP:probinson[2019-03-10];HP:probinson[2019-03-10]
OMIM:604173	Poikiloderma with neutropenia		HP:0001510	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000982	PMID:20503306	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000347	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0000962	PMID:20734427	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0001875	PMID:20734427;PMID:20004881;PMID:20503306	PCS		19/19			P	HP:probinson[2019-03-10];HPO:skoehler[2012-10-17];HP:probinson[2019-03-10];HPO:probinson[2022-03-26]
OMIM:604173	Poikiloderma with neutropenia		HP:0005338	PMID:20734427	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:236450	Hutterite cerebroosteonephrodysplasia syndrome		HP:0004322	OMIM:236450	PCS					P	HPO:probinson[2012-03-17]
OMIM:236450	Hutterite cerebroosteonephrodysplasia syndrome		HP:0000100	OMIM:236450	PCS					P	HPO:probinson[2012-03-17]
OMIM:236450	Hutterite cerebroosteonephrodysplasia syndrome		HP:0000007	OMIM:236450	PCS		20/20			I	HPO:probinson[2012-03-17];HPO:iea[2009-02-17]
OMIM:236450	Hutterite cerebroosteonephrodysplasia syndrome		HP:0008872	OMIM:236450	PCS					P	HPO:probinson[2012-03-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0002444	PMID:30497210	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0002983	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0001770	PMID:30497210	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0003577	PMID:30497210	PCS		2/2			C	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0002089	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0004322	PMID:30497210	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000161	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0002085	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0003196	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0010820	PMID:30497210	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0030680	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000238	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0001522	OMIM:241800	TAS		HP:0040282			C	HPO:probinson[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000256	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000773	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000830	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000110	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0002652	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000175	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000252	PMID:30497210	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000054	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0030765	PMID:30497210	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000750	PMID:30497210	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0001162	PMID:30497210	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000171	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0005280	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0007099	PMID:30497210	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0002827	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000007	PMID:30497210	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0009733	OMIM:241800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:241800	Pallister-Hall-like syndrome		HP:0001830	PMID:30497210	PCS		2/2			P	HPO:probinson[2022-10-24]
OMIM:241800	Pallister-Hall-like syndrome		HP:0000347	OMIM:241800	IEA					P	HPO:iea[2009-02-17]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001276	PMID:26299366	PCS		3/14			P	HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0003577	PMID:26299366	PCS		4/14			C	HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0002188	PMID:26299366	PCS		2/12			P	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0002540	PMID:26299366	PCS		12/12			P	HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0000486	PMID:26299366	PCS		2/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0004322	PMID:26299366	PCS		2/14			P	HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001250	PMID:26299366	PCS		13/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001252	PMID:26299366	PCS		12/14			P	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0002020	PMID:26299366	PCS		4/14			P	HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0003593	PMID:26299366	PCS		10/14			C	HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0033725	PMID:26299366	PCS		2/12			P	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001508	PMID:26299366	PCS		6/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0000639	PMID:26299366	PCS		3/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0100704	PMID:26299366	PCS		9/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0012450	PMID:26299366	PCS		3/14			P	HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0003429	PMID:26299366	PCS		1/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0008936	PMID:26299366	PCS		3/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0000252	PMID:26299366	PCS		12/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001344	PMID:26299366	PCS		13/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0002353	PMID:26299366	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0002650	PMID:26299366	PCS		4/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0002079	PMID:26299366	PCS		1/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0011968	PMID:26299366	PCS		9/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001263	PMID:26299366	PCS		14/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0000407	PMID:26299366	PCS		14/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0000007	PMID:26299366	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0000505	PMID:26299366	PCS		13/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001257	PMID:26299366	PCS		9/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0001873	PMID:26299366	PCS		3/14			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:616577	Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities		HP:0002721	PMID:26299366	PCS		4/12			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002202	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002783	PMID:33876776	PCS		6/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0000100	PMID:33876776	PCS		3/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002384	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0001250	PMID:33876776	PCS		7/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0005575	PMID:33876776	PCS		1/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0000083	PMID:33876776	PCS		4/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0003593	PMID:33876776	PCS		2/4			C	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002240	PMID:33876776	PCS		13/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002480	PMID:33876776	PCS		1/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0011897	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0012156	PMID:33876776	PCS		6/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0012311	PMID:33876776	PCS		3/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0001508	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0040197	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0011463	PMID:33876776	PCS		1/4			C	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0031691	PMID:33876776	PCS		15/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0100702	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0006530	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002716	PMID:33876776	PCS		2/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0006532	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0025435	PMID:33876776	PCS		10/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0006554	PMID:33876776	PCS		3/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0001522	PMID:33876776	PCS		7/15			C	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002910	PMID:33876776	PCS		12/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002514	PMID:33876776	PCS		3/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0005548	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0003565	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0003621	PMID:33876776	PCS		1/4			C	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0002254	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0000793	PMID:33876776	PCS		1/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0001263	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0020087	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0033399	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0011227	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0040223	PMID:33876776	PCS		6/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0032271	PMID:33876776	PCS		2/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0000969	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0003819	PMID:33876776	PCS		4/15			C	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0040186	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0000729	PMID:33876776	PCS		2/15			P	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0000007	PMID:33876776	PCS					I	HPO:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0001954	PMID:33876776	PCS		1/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0001433	PMID:33876776	PCS		2/4			P	HP:probinson[2022-02-14]
OMIM:619644	Immunodeficiency 91 and hyperinflammation		HP:0001873	PMID:33876776	PCS		2/4			P	HP:probinson[2022-02-14]
OMIM:606764	Gastrointestinal stromal tumor		HP:0001067	OMIM:606764	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606764	Gastrointestinal stromal tumor		HP:0001176	OMIM:606764	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606764	Gastrointestinal stromal tumor		HP:0002015	OMIM:606764	IEA					P	HPO:skoehler[2010-06-19]
OMIM:606764	Gastrointestinal stromal tumor		HP:0001025	OMIM:606764	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606764	Gastrointestinal stromal tumor		HP:0005214	OMIM:606764	IEA					P	HPO:skoehler[2010-06-19]
OMIM:606764	Gastrointestinal stromal tumor		HP:0100723	OMIM:606764	TAS					P	HPO:skoehler[2013-05-29]
OMIM:606764	Gastrointestinal stromal tumor		HP:0000953	OMIM:606764	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606764	Gastrointestinal stromal tumor		HP:0003745	OMIM:606764	IEA					I	HPO:skoehler[2010-06-19]
OMIM:606764	Gastrointestinal stromal tumor		HP:0002019	OMIM:606764	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606764	Gastrointestinal stromal tumor		HP:0000006	OMIM:606764	IEA					I	HPO:skoehler[2010-06-19]
OMIM:300848	Intellectual developmental disorder, X-linked 89		HP:0000750	OMIM:300848	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300848	Intellectual developmental disorder, X-linked 89		HP:0002123	OMIM:300848	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300848	Intellectual developmental disorder, X-linked 89		HP:0001263	OMIM:300848	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300848	Intellectual developmental disorder, X-linked 89		HP:0001423	OMIM:300848	TAS					I	HPO:skoehler[2012-10-14]
OMIM:300848	Intellectual developmental disorder, X-linked 89		HP:0001249	OMIM:300848	TAS					P	HPO:skoehler[2015-01-27]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0001276	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000286	PMID:11815777	PCS		2/3			P	HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000486	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0001332	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0001250	PMID:8040306;PMID:11815777	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12];HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0001252	PMID:8040306	PCS		2/2			P	HPO:probinson[2022-12-12]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0002240	OMIM:264470	PCS				HP:0012825	P	HPO:probinson[2012-04-11]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0003593	OMIM:264470	PCS					C	HPO:probinson[2012-04-11]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000580	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:6000217	PMID:11815777	PCS		3/3			P	HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000639	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000737	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000316	PMID:11815777	PCS		2/3			P	HPO:probinson[2012-04-11];HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0006555	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000510	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0002910	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0002415	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0007305	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000654	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0003623	PMID:8040306	PCS		2/2			C	HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0002015	PMID:11815777	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0008619	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000431	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0003487	PMID:11815777	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0002376	PMID:11815777	PCS		3/3			P	HPO:probinson[2012-04-11];HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0003186	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0011344	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0005280	PMID:11815777	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0008167	PMID:8040306	PCS		2/2			P	HPO:probinson[2022-12-12]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0008763	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000007	PMID:8040306	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0001319	PMID:8040306	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000648	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0002007	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000248	OMIM:264470	IEA					P	HPO:iea[2009-02-17]
OMIM:264470	Peroxisomal acyl-CoA oxidase deficiency		HP:0000369	PMID:11815777	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0001298	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0003577	PMID:28777934	PCS		2/3			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0002521	PMID:28777934	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0003676	PMID:28777934	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0000365	PMID:28777934	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0001332	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0002120	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0001250	PMID:28777934	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0001274	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0003593	PMID:28777934	PCS		1/3			C	HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0012110	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0100704	PMID:28777934	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0002119	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0008936	PMID:28777934	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0000011	PMID:28777934	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0002015	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0000252	PMID:28777934	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0002650	PMID:28777934	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0002376	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0001321	PMID:28777934	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0011968	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0011344	PMID:28777934	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0012510	PMID:28777934	PCS		3/3			P	HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0011097	PMID:28777934	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0034353	PMID:28777934	PCS		3/3			P	HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0034311	PMID:28777934	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0000007	PMID:28777934	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0000648	PMID:28777934	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0001336	PMID:28777934	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617669	Encephalopathy, progressive, early-onset, with brain atrophy and spasticity		HP:0009879	PMID:28777934	PCS		3/3			P	HPO:probinson[2023-02-21]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0003477	PMID:16636238	PCS		8/8			P	HPO:iea[2010-09-07]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0003236	OMIM:606002	TAS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0003676	OMIM:606002	TAS					C	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0000486	OMIM:606002	TAS		30%			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0000640	OMIM:606002	TAS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0003431	OMIM:606002	TAS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001332	PMID:14736755	PCS		5/18			P	HPO:iea[2010-09-08]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0003693	PMID:16636238	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001272	PMID:16636238;PMID:14736755;PMID:19141356	PCS		39/39			P	HPO:iea[2010-09-07];HPO:iea[2010-09-08]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0002066	PMID:16636238;PMID:14736755	PCS		23/28			P	HPO:iea[2010-09-08];HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001271	OMIM:606002	TAS					P	HPO:skoehler[2013-06-23]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001152	OMIM:606002	TAS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0002460	PMID:16636238	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0010702	OMIM:606002	TAS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0000639	PMID:16636238;PMID:19141356	PCS		15/29			P	HPO:iea[2010-09-07];HPO:iea[2010-09-08]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0007240	OMIM:606002	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0003828	OMIM:606002	TAS					M	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0000657	PMID:16636238;PMID:14736755;PMID:19141356	PCS		18/47			P	HPO:iea[2010-09-08];HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0006254	PMID:16636238;PMID:14736755;PMID:19141356	PCS		43/43			P	HPO:iea[2010-09-08];HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0007267	OMIM:606002	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001265	PMID:14736755	PCS		4/18			P	HPO:iea[2010-09-08]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0002015	PMID:16636238	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0006879	OMIM:606002	TAS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0002650	PMID:14736755	PCS		7/18			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001761	PMID:14736755	PCS		12/18			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0006937	OMIM:606002	TAS		57%			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001260	PMID:16636238	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001284	PMID:16636238;PMID:19141356;PMID:14736755	PCS		41/47			P	HPO:iea[2010-09-08];HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0002072	OMIM:606002	TAS		4/18			P	HPO:iea[2010-09-08]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0002070	OMIM:606002	TAS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0010831	PMID:16636238	PCS		10/10			P	HPO:iea[2010-09-07]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0000007	OMIM:606002	TAS					I	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0000524	OMIM:606002	TAS		HP:0040283			P	HPO:skoehler[2013-06-23]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0007256	OMIM:606002	TAS					P	HPO:skoehler[2014-11-26]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0006886	PMID:16636238	PCS					P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001337	OMIM:606002	TAS		57%			P	HPO:iea[2009-02-17]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0001315	PMID:14736755	PCS		18/18			P	HPO:iea[2010-09-08]
OMIM:606002	Spinocerebellar ataxia, autosomal recessive 1		HP:0002346	PMID:14736755;PMID:19141356	PCS		7/37			P	HPO:iea[2010-09-08]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002069	PMID:30356099	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000286	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002188	PMID:25411445;PMID:30356099	PCS		2/26			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002266	PMID:25411445;PMID:30356099	PCS		6/26			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0001250	PMID:24456803;PMID:25411445	PCS		2/2		HP:0031375	P	HPO:skoehler[2015-02-22];HPO:probinson[2023-02-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002063	PMID:25411445	PCS		2/6			P	HPO:skoehler[2015-02-22]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0001251	PMID:25411445	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0003593	PMID:24456803;PMID:25411445;PMID:30356099	PCS		15/25			C	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0033725	PMID:25411445;PMID:30356099	PCS		17/25			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000311	PMID:30356099	PCS		4/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000512	PMID:24456803;PMID:25411445;PMID:30356099	PCS		7/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-02-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0003623	PMID:25411445;PMID:30356099	PCS		10/24			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0001188	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000253	OMIM:616211	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000252	OMIM:616211	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002353	PMID:25411445;PMID:30356099	PCS		24/24			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002079	PMID:24456803	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0001263	PMID:24456803;PMID:25411445;PMID:30356099	PCS		27/27		HP:0012829	P	HPO:skoehler[2015-02-22];HPO:probinson[2023-02-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0011169	PMID:25411445;PMID:30356099	PCS		1/26			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0033258	PMID:25411445	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0011097	PMID:25411445;PMID:30356099	PCS		9/26			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0010880	PMID:25411445	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000007	PMID:24456803	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000648	PMID:25411445;PMID:30356099	PCS		4/22			P	HPO:skoehler[2015-02-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0001257	PMID:25411445;PMID:30356099	PCS		13/19			P	HPO:skoehler[2015-02-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000341	PMID:24456803;PMID:30356099	PCS		4/21			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000582	PMID:30356099	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000343	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000463	PMID:24456803;PMID:30356099	PCS		3/21			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002121	PMID:25411445;PMID:30356099	PCS		2/26			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0011167	PMID:25411445;PMID:30356099	PCS		3/26			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000817	PMID:25411445;PMID:30356099	PCS		19/25			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002514	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0001347	PMID:24456803;PMID:25411445	PCS		4/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-02-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0008936	PMID:25411445;PMID:30356099	PCS		10/15			P	HPO:skoehler[2015-02-22];HPO:probinson[2024-03-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002059	PMID:24456803;PMID:25411445;PMID:30356099	PCS		13/27			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-02-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002375	PMID:25411445;PMID:30356099	PCS		20/25			P	HPO:skoehler[2015-02-22];HPO:probinson[2024-03-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002133	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000592	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0005484	PMID:25411445	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000470	PMID:30356099	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0009909	PMID:30356099	PCS		4/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0001558	PMID:30356099	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000348	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000546	PMID:25411445	PCS		1/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2024-03-27]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0007334	PMID:25411445;PMID:30356099	PCS		6/26			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0200134	PMID:24456803;PMID:25411445;PMID:30356099	PCS		27/27			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-02-27];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0002007	PMID:30356099	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0000347	PMID:30356099	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616211	Developmental and epileptic encephalopathy 28		HP:0009879	PMID:24456803	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000176	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000286	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0003577	PMID:31215115	PCS					C	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000463	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000023	PMID:31215115	PCS		3/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0001382	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000391	PMID:31215115	PCS		5/12			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000592	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0003691	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0011800	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0100333	PMID:31215115	PCS		2/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0011261	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0100334	PMID:31215115	PCS		2/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000349	PMID:31215115	PCS		1/5			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000767	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0005815	PMID:31215115	PCS		5/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0001763	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0002558	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000006	PMID:31215115	PCS					I	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000347	PMID:31215115	PCS		1/6			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0008416	PMID:31215115	PCS		3/6			P	HPO:probinson[2021-02-13]
OMIM:619122	Vertebral hypersegmentation and orofacial anomalies		HP:0000269	PMID:31215115	PCS		1/5			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:617127	Orofaciodigital syndrome XV		HP:0001320	PMID:26643951	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0003577	PMID:26643951	PCS		1/1			C	HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0000431	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0000463	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0001162	PMID:26643951	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0001274	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0000180	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0012368	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0009084	PMID:26643951	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0010055	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0010066	PMID:26643951	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0000316	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0000007	PMID:26643951	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0002419	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0002119	PMID:26643951	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0000369	PMID:26643951	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:617127	Orofaciodigital syndrome XV		HP:0000126	PMID:26643951	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-10]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0002069	PMID:17928598	PCS					P	HPO:probinson[2013-01-09]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0001297	OMIM:611556	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0031295	OMIM:611556	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0000007	PMID:17928598	PCS					I	HPO:probinson[2013-04-04]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0001712	OMIM:611556	TAS					P	HPO:skoehler[2014-08-24]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0001638	PMID:17928598	PCS					P	HPO:probinson[2013-04-04]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0012270	PMID:17928598	PCS					P	HPO:probinson[2013-04-07]
OMIM:611556	Glycogen storage disease 0, muscle		HP:0003546	PMID:17928598	PCS					P	HPO:probinson[2013-04-04]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003236	PMID:25385316	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0000365	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001272	OMIM:616239	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003198	OMIM:616239	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001250	PMID:25385316	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001274	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001252	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003593	PMID:25385316	PCS		2/2			C	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001290	OMIM:616239	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002180	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0030319	PMID:25385316	PCS		1/2			P	HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0000639	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0100704	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003429	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001324	OMIM:616239	TAS				HP:0012840	P	HPO:skoehler[2015-03-22]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003701	PMID:25385316	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001347	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001265	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003202	PMID:25385316	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0000252	OMIM:616239	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002133	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003200	PMID:25385316	PCS		2/2			P	HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002376	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002079	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0003388	PMID:25385316	PCS		1/2			P	HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0011968	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001260	PMID:25385316	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0000097	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001263	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002151	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001284	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002171	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002490	OMIM:616239	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0011923	PMID:25385316	PCS		2/2			P	HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0000508	PMID:25385316	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0200114	OMIM:616239	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0000007	PMID:25385316	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0002529	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0000648	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0008347	PMID:25385316	PCS		2/2			P	HPO:probinson[2023-03-12]
OMIM:616239	Combined oxidative phosphorylation deficiency 24		HP:0001257	OMIM:616239	TAS					P	HPO:skoehler[2015-12-30]
OMIM:162091	Schwannomatosis		HP:0009593	PMID:17357086	PCS		2/2			P	HPO:probinson[2022-10-11]
OMIM:162091	Schwannomatosis		HP:0001442	OMIM:162091	TAS					I	HPO:skoehler[2012-11-18]
OMIM:162091	Schwannomatosis		HP:0003581	PMID:17357086	PCS		2/2			C	HPO:probinson[2022-10-11]
OMIM:162091	Schwannomatosis		HP:0003829	OMIM:162091	IEA					I	HPO:iea[2009-02-17]
OMIM:162091	Schwannomatosis		HP:0010302	PMID:17357086	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-11]
OMIM:162091	Schwannomatosis		HP:0002858	OMIM:162091	TAS					P	HPO:skoehler[2012-11-18]
OMIM:162091	Schwannomatosis		HP:0009588	PMID:17357086	PCS		0/2			P	HPO:probinson[2022-10-11]
OMIM:162091	Schwannomatosis		HP:0000006	PMID:17357086	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:613341	Leber congenital amaurosis 14		HP:0000550	OMIM:613341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613341	Leber congenital amaurosis 14		HP:0000662	OMIM:613341	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613341	Leber congenital amaurosis 14		HP:0000980	OMIM:613341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613341	Leber congenital amaurosis 14		HP:0000639	OMIM:613341	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613341	Leber congenital amaurosis 14		HP:0000613	OMIM:613341	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613341	Leber congenital amaurosis 14		HP:0000007	OMIM:613341	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613341	Leber congenital amaurosis 14		HP:0007663	OMIM:613341	TAS					P	HPO:skoehler[2015-07-26]
OMIM:613341	Leber congenital amaurosis 14		HP:0002527	OMIM:613341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613341	Leber congenital amaurosis 14		HP:0000510	OMIM:613341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613341	Leber congenital amaurosis 14		HP:0007875	OMIM:613341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613341	Leber congenital amaurosis 14		HP:0000543	OMIM:613341	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613341	Leber congenital amaurosis 14		HP:0000556	OMIM:613341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613341	Leber congenital amaurosis 14		HP:0000654	OMIM:613341	IEA					P	HPO:skoehler[2010-06-20]
OMIM:237000	HYDROXYPROLINEMIA		HP:0002907	OMIM:237000	IEA					P	HPO:iea[2009-02-17]
OMIM:237000	HYDROXYPROLINEMIA		HP:0003260	OMIM:237000	IEA					P	HPO:iea[2009-02-17]
OMIM:237000	HYDROXYPROLINEMIA		HP:0000007	OMIM:237000	IEA					I	HPO:iea[2009-02-17]
OMIM:237000	HYDROXYPROLINEMIA		HP:0001249	OMIM:237000	IEA					P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0000750	OMIM:209850	IEA					P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0002353	OMIM:209850	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0001250	OMIM:209850	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0003144	OMIM:209850	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0011463	OMIM:209850	IEA					C	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0000717	OMIM:209850	IEA					P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0000728	OMIM:209850	IEA					P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0000723	OMIM:209850	TAS					P	HPO:skoehler[2013-06-04]
OMIM:209850	Autism susceptibility 1		HP:0000733	OMIM:209850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0001426	OMIM:209850	IEA					I	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0000758	OMIM:209850	TAS					P	HPO:probinson[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0003745	OMIM:209850	IEA					I	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0000721	OMIM:209850	IEA					P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0000732	OMIM:209850	IEA					P	HPO:iea[2009-02-17]
OMIM:209850	Autism susceptibility 1		HP:0001249	OMIM:209850	IEA					P	HPO:iea[2009-02-17]
OMIM:165098	Ophthalmoplegia, familial total, with iris transillumination		HP:0007824	OMIM:165098	IEA					P	HPO:iea[2009-02-17]
OMIM:165098	Ophthalmoplegia, familial total, with iris transillumination		HP:0000508	OMIM:165098	IEA					P	HPO:iea[2009-02-17]
OMIM:165098	Ophthalmoplegia, familial total, with iris transillumination		HP:0007942	OMIM:165098	IEA					P	HPO:iea[2009-02-17]
OMIM:165098	Ophthalmoplegia, familial total, with iris transillumination		HP:0000006	OMIM:165098	IEA					I	HPO:iea[2009-02-17]
OMIM:165098	Ophthalmoplegia, familial total, with iris transillumination		HP:0000544	OMIM:165098	IEA					P	HPO:iea[2009-02-17]
OMIM:165098	Ophthalmoplegia, familial total, with iris transillumination		HP:0000577	OMIM:165098	IEA					P	HPO:iea[2009-02-17]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0002465	PMID:16909393	PCS		1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0004324	PMID:20412111	PCS		1/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000582	PMID:16909393;PMID:20412111	PCS		3/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0010529	PMID:20412111	PCS		3/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0001773	PMID:16909393	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0001250	PMID:16909393;PMID:20412111	PCS		6/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0002162	PMID:16909393;PMID:20412111	PCS		6/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000283	PMID:16909393	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000085	PMID:20412111	PCS		1/5			P	HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0003593	PMID:20412111	PCS		5/5			C	HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0005590	PMID:20412111	PCS		2/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0010721	PMID:16909393;PMID:20412111	PCS		6/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000958	PMID:16909393	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0010055	PMID:20412111	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000718	PMID:20412111	PCS		2/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000316	PMID:16909393;PMID:20412111	PCS		1/8			P	HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0007103	PMID:16909393	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0002714	PMID:16909393	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0006610	PMID:16909393;PMID:20412111	PCS		7/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000256	PMID:20412111	PCS		1/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0001763	PMID:16909393	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0001007	PMID:16909393;PMID:20412111	PCS		7/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0001249	PMID:20412111	PCS		4/4			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000336	PMID:20412111	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000154	PMID:16909393;PMID:20412111	PCS		7/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000054	PMID:16909393;PMID:20412111	PCS		7/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000475	PMID:16909393	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000233	PMID:16909393	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0001344	PMID:16909393;PMID:20412111	PCS		3/8			P	HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000750	PMID:20412111	PCS		5/5			P	HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000490	PMID:20412111	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000272	PMID:16909393	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000470	PMID:16909393;PMID:20412111	PCS		6/8			P	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0004691	PMID:20412111	PCS		1/5			P	HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0011800	PMID:16909393	PCS		2/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0005280	PMID:16909393;PMID:20412111	PCS		3/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0001419	PMID:16909393	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0100716	PMID:20412111	PCS		2/5			P	HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0007874	PMID:20412111	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0008404	PMID:16909393;PMID:20412111	PCS		4/8			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300860	Intellectual developmental disorder, X-linked syndromic, Nascimento type		HP:0000664	PMID:16909393;PMID:20412111	PCS		8/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2012-10-14];HPO:probinson[2021-09-26]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0002059	OMIM:617899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0000252	OMIM:617899	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001344	OMIM:617899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0000365	OMIM:617899	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001332	OMIM:617899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001272	OMIM:617899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001250	OMIM:617899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0011968	OMIM:617899	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001290	OMIM:617899	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0002093	OMIM:617899	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0000618	OMIM:617899	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0000007	OMIM:617899	IEA					I	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001257	OMIM:617899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001510	OMIM:617899	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617899	Leukodystrophy, hypomyelinating, 14		HP:0001249	OMIM:617899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0000252	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0002540	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0001344	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0002057	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0004322	PMID:28542170	PCS		2/2			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0001321	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0001250	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0001263	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0032388	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0000316	PMID:28542170	PCS		2/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0001845	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0000007	PMID:28542170	PCS					I	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0000648	PMID:28542170	PCS		2/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618572	Neurodevelopmental disorder with cerebellar hypoplasia and spasticity		HP:0001258	PMID:28542170	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000286	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000365	PMID:28566479	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000486	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000463	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0030037	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0002002	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000089	PMID:28566479	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000122	PMID:28566479	PCS	HP:0003577	1/5			P	HPO:probinson[2020-09-12]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000062	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000083	OMIM:617641	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000086	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000085	PMID:28566479	PCS	HP:0003577	1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0001290	OMIM:617641	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0001270	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0040080	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0004719	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0008551	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0002617	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0001627	OMIM:617641	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000219	OMIM:617641	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000377	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000776	OMIM:617641	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000275	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0001562	OMIM:617641	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000110	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000054	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000076	OMIM:617641	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000750	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000431	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000276	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0011968	OMIM:617641	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0005564	PMID:28566479	PCS		1/5			P	HPO:probinson[2020-09-12]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0005563	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000391	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0001263	PMID:28566479	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0002093	OMIM:617641	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0001999	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0008589	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0001510	OMIM:617641	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000006	OMIM:617641	IEA					I	HPO:skoehler[2019-04-18]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000028	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000369	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617641	Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		HP:0000104	OMIM:617641	IEA					P	HPO:skoehler[2018-10-08]
OMIM:157980	MOMO syndrome		HP:0000286	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0001176	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000486	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000684	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0001795	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000343	OMIM:157980	TAS					P	HPO:probinson[2012-05-01]
OMIM:157980	MOMO syndrome		HP:0000480	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000639	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000319	OMIM:157980	TAS					P	HPO:probinson[2012-05-01]
OMIM:157980	MOMO syndrome		HP:0000618	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000316	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000679	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0001548	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000337	OMIM:157980	TAS					P	HPO:probinson[2012-05-01]
OMIM:157980	MOMO syndrome		HP:0000879	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000218	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0008577	OMIM:157980	TAS					P	HPO:probinson[2012-05-01]
OMIM:157980	MOMO syndrome		HP:0000179	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000256	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0001249	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000494	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000431	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0002750	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000470	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000965	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000689	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0001833	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000348	OMIM:157980	TAS					P	HPO:probinson[2012-05-01]
OMIM:157980	MOMO syndrome		HP:0000625	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0002007	OMIM:157980	TAS					P	HPO:skoehler[2012-10-17]
OMIM:157980	MOMO syndrome		HP:0000006	OMIM:157980	IEA					I	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000248	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0001513	OMIM:157980	IEA					P	HPO:iea[2009-02-17]
OMIM:157980	MOMO syndrome		HP:0000501	OMIM:157980	TAS					P	HPO:skoehler[2012-10-17]
OMIM:100600	Acanthosis nigricans		HP:0000956	OMIM:100600	IEA					P	HPO:iea[2009-02-17]
OMIM:100600	Acanthosis nigricans		HP:0000006	OMIM:100600	IEA					I	HPO:iea[2009-02-17]
OMIM:184500	Steatocystoma multiplex		HP:0000695	PMID:9008238	PCS		0/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:184500	Steatocystoma multiplex		HP:0012035	PMID:9008238	PCS		10/10			P	HPO:probinson[2012-07-27];HPO:probinson[2024-03-08]
OMIM:184500	Steatocystoma multiplex		HP:0000006	PMID:9008238	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0003577	OMIM:615042	TAS					C	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0003236	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0000486	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0001250	OMIM:615042	TAS				HP:0031375	P	HPO:skoehler[2013-06-06]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0006829	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0003196	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0001290	PMID:19901254	TAS				HP:0012828	P	HPO:nvasilevsky[2019-03-27]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0000219	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0000218	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0001522	OMIM:615042	TAS					C	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002910	PMID:19901254	IEA					P	HPO:nvasilevsky[2019-03-27]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002058	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002476	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002650	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002375	OMIM:615042	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0001321	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0011968	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002098	OMIM:615042	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0001263	PMID:19901254	TAS					P	HPO:skoehler[2013-02-25];HPO:nvasilevsky[2019-03-27]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0005484	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0410362	OMIM:615042	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0003160	PMID:23109149	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0012762	PMID:19901254	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002803	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0000007	OMIM:615042	TAS					I	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0000601	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0000648	OMIM:615042	TAS		HP:0040282			P	HPO:skoehler[2013-06-03]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0000347	OMIM:615042	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615042	Congenital disorder of glycosylation, type Iu		HP:0002643	PMID:19901254	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:615724	Premature ovarian failure 9		HP:0008209	PMID:24597873	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-08]
OMIM:615724	Premature ovarian failure 9		HP:0011969	PMID:24597873	PCS		3/3			P	HPO:probinson[2023-03-08]
OMIM:615724	Premature ovarian failure 9		HP:0000141	PMID:24597873	PCS		3/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-08]
OMIM:615724	Premature ovarian failure 9		HP:0011462	PMID:24597873	PCS		3/3			C	HPO:probinson[2023-03-08]
OMIM:615724	Premature ovarian failure 9		HP:0008232	PMID:24597873	PCS		3/3			P	HPO:probinson[2023-03-08]
OMIM:615724	Premature ovarian failure 9		HP:0000007	PMID:24597873	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-08]
OMIM:615724	Premature ovarian failure 9		HP:0008724	PMID:24597873	PCS		3/3			P	HPO:probinson[2023-03-08]
OMIM:104300	Alzheimer disease		HP:0001300	OMIM:104300	TAS					P	HPO:probinson[2009-02-17]
OMIM:104300	Alzheimer disease		HP:0000726	OMIM:104300	TAS					P	HPO:skoehler[2010-06-20]
OMIM:104300	Alzheimer disease		HP:0003581	OMIM:104300	TAS					C	HPO:probinson[2022-04-17]
OMIM:104300	Alzheimer disease		HP:0002185	OMIM:104300	TAS					P	HPO:probinson[2009-02-17]
OMIM:104300	Alzheimer disease		HP:0410054	PMID:17031479	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:104300	Alzheimer disease		HP:0000006	OMIM:104300	TAS					I	HPO:probinson[2009-02-17]
OMIM:104300	Alzheimer disease		HP:0002423	OMIM:104300	TAS					P	HPO:probinson[2009-02-17]
OMIM:104300	Alzheimer disease		HP:0002511	OMIM:104300	TAS					P	HPO:probinson[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0000175	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0000365	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0004322	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0001417	OMIM:302905	IEA					I	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0000400	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0000411	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0000047	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0000589	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:302905	Charge-Like syndrome, X-linked		HP:0002974	OMIM:302905	IEA					P	HPO:iea[2009-02-17]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0000286	PMID:20206336	PCS		2/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0000365	PMID:20206336	PCS		2/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0010605	PMID:20206336	PCS		1/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0004322	PMID:20206336	PCS		1/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0100694	PMID:20206336	PCS		1/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0000718	PMID:20206336	PCS		2/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001647	PMID:20206336	PCS		1/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0000316	PMID:20206336	PCS		1/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0100807	PMID:20206336	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0008897	PMID:20206336	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001643	PMID:20206336	PCS		3/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0003745	PMID:20206336	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001466	PMID:20206336	PCS					I	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001763	PMID:20206336	PCS		2/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0000358	PMID:20206336	PCS		1/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0000252	PMID:20206336	PCS		5/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001762	OMIM:613355	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0002650	PMID:20206336	PCS		2/7			P	HPO:probinson[2023-06-09];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001684	PMID:20206336	PCS		2/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001263	PMID:20206336	PCS		7/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0010511	PMID:20206336	PCS		6/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0002092	PMID:20206336	PCS		3/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0005280	PMID:20206336	PCS		1/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001518	PMID:20206336	PCS		5/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0000565	PMID:20206336	PCS		2/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001357	PMID:20206336	PCS		1/7			P	HPO:probinson[2023-06-09]
OMIM:613355	Chromosome 17q23.1-q23.2 deletion syndrome		HP:0001238	PMID:20206336	PCS		6/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-09]
OMIM:180000	Retinal arteries, tortuosity of		HP:0000572	PMID:25228067	PCS		0/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-02-20]
OMIM:180000	Retinal arteries, tortuosity of		HP:0000573	PMID:25228067	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:180000	Retinal arteries, tortuosity of		HP:0003581	PMID:25228067	PCS		3/3			C	HPO:probinson[2022-02-20]
OMIM:180000	Retinal arteries, tortuosity of		HP:0000613	PMID:25228067	PCS		1/3			P	HPO:probinson[2022-02-20]
OMIM:180000	Retinal arteries, tortuosity of		HP:0001136	PMID:25228067	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:180000	Retinal arteries, tortuosity of		HP:0000006	PMID:25228067	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0003676	PMID:26872069	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0003621	PMID:26872069	PCS		1/2			C	HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0000518	PMID:26872069	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0001272	PMID:26872069	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0001260	PMID:26872069	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0002066	PMID:26872069	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0011463	PMID:26872069	PCS		1/2			C	HPO:probinson[2023-03-26];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0002064	PMID:26872069	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0000007	PMID:26872069	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0002070	PMID:26872069	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-26]
OMIM:617133	Spinocerebellar ataxia, autosomal recessive 24		HP:0000666	PMID:26872069	PCS		2/2			P	HPO:probinson[2023-03-26]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002344	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0004325	PMID:10352942	PCS	HP:0003577				P	HP:probinson[2019-01-27]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0010803	OMIM:608013	TAS					P	HPO:probinson[2012-04-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000486	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0005257	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001250	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000160	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0003196	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0011461	PMID:8929950	PCS		1/1			C	HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000316	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000278	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0007549	OMIM:608013	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000252	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001541	OMIM:608013	TAS					P	HPO:probinson[2012-04-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000007	PMID:8929950	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000967	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002304	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0007479	PMID:10685993	PCS	HP:0003577	6/6			P	HPO:probinson[2012-04-17];HP:probinson[2019-01-27]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002104	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000369	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000325	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000962	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001399	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002089	PMID:8929950	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000463	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002240	PMID:8929950	PCS		1/1			P	HPO:iea[2009-02-17];HP:probinson[2019-01-27];HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001790	PMID:8929950	PCS		1/1			P	HPO:iea[2009-02-17];HP:probinson[2019-01-27];HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001903	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000979	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0008551	OMIM:608013	TAS					P	HPO:probinson[2012-04-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002119	OMIM:608013	TAS					P	HPO:skoehler[2014-05-04]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001744	PMID:8929950	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001622	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002179	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002015	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001561	PMID:3415310	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-01-27]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002375	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001640	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000232	OMIM:608013	TAS					P	HPO:probinson[2012-04-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000194	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002098	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0005280	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0008064	OMIM:608013	TAS					P	HPO:probinson[2012-04-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0002804	PMID:8929950	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001558	PMID:8929950	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000741	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001511	OMIM:608013	IEA					P	HPO:iea[2009-02-17]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0003811	PMID:8929950	PCS		1/1			C	HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001873	PMID:8929950	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0001433	PMID:10649495	PCS					P	HP:probinson[2019-01-27]
OMIM:608013	Gaucher disease, perinatal lethal		HP:0000347	OMIM:608013	TAS					P	HPO:probinson[2012-04-17]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000286	PMID:26765342	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0010749	PMID:26765342	PCS		3/10			P	HPO:probinson[2023-01-30];HPO:skoehler[2010-06-18];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0003577	PMID:26765342	PCS		3/4			C	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001476	PMID:26765342	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000222	PMID:26765342	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001058	PMID:26765342	PCS		4/5			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0010648	PMID:26765342	PCS		3/3			P	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000023	OMIM:225410	IEA					P	HPO:iea[2009-02-17]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0004322	OMIM:225410	IEA					P	HPO:iea[2009-02-17]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001030	PMID:26765342	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000260	PMID:26765342	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0005332	OMIM:225410	IEA					P	HPO:iea[2009-02-17]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001075	PMID:26765342	PCS		3/4			P	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0003593	PMID:26765342	PCS		1/4			C	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001270	PMID:26765342	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000938	OMIM:225410	IEA					P	HPO:iea[2009-02-17]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0012471	OMIM:225410	TAS					P	HPO:skoehler[2014-11-26]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000978	PMID:26765342	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0008897	PMID:26765342	PCS		5/5			P	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001027	PMID:26765342	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000212	OMIM:225410	IEA		6/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001007	PMID:26765342	PCS		2/4		HP:0012825	P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000974	PMID:26765342	PCS		4/4			P	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001788	PMID:26765342	PCS		6/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0009803	OMIM:225410	IEA					P	HPO:iea[2009-02-17]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001622	PMID:26765342	PCS		9/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0004876	PMID:26765342	PCS		1/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000494	PMID:26765342	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0009826	PMID:26765342	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000232	OMIM:225410	IEA					P	HPO:iea[2009-02-17]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001382	PMID:26765342	PCS		5/5		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000592	PMID:26765342	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001582	PMID:26765342	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0200094	OMIM:225410	TAS					P	HPO:skoehler[2013-06-04]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000506	PMID:26765342	PCS		2/5			P	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000668	PMID:26765342	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001537	PMID:26765342	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000007	PMID:10417273	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000369	PMID:26765342	PCS		2/5			P	HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000347	PMID:26765342	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000545	PMID:26765342	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0000225	PMID:26765342	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:225410	Ehlers-Danlos syndrome, dermatosparaxis type		HP:0001831	OMIM:225410	IEA					P	HPO:iea[2009-02-17]
OMIM:149200	Bart-Pumphrey syndrome		HP:0003577	PMID:15482471	PCS		4/4			C	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:149200	Bart-Pumphrey syndrome		HP:0000365	PMID:15482471	PCS	HP:0003577	4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-28]
OMIM:149200	Bart-Pumphrey syndrome		HP:0032541	PMID:15482471	PCS		2/4			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:149200	Bart-Pumphrey syndrome		HP:0000982	PMID:15482471	PCS		4/4			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:149200	Bart-Pumphrey syndrome		HP:0000006	PMID:15482471	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:149200	Bart-Pumphrey syndrome		HP:0001820	PMID:15482471	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0002069	PMID:36073542	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0001332	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0002384	PMID:36073542	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0001252	PMID:36073542	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0003593	PMID:36073542	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0032794	PMID:36073542	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0001270	PMID:36073542	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0008070	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0033725	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0010721	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0011463	PMID:36073542	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000718	PMID:36073542	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0007166	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0012450	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000316	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000238	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0002119	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0001249	PMID:36073542	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000577	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000494	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0002059	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000750	PMID:36073542	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0002133	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0002376	PMID:36073542	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0010819	PMID:36073542	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000490	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0001263	PMID:36073542	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0009909	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0002072	PMID:36073542	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0100021	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0001182	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0010535	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0007270	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000729	PMID:36073542	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0008523	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0100716	PMID:36073542	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0001852	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000664	PMID:36073542	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:620774	Developmental and epileptic encephalopathy 114		HP:0000006	PMID:36073542	PCS					I	ORCID:0000-0002-0736-9199[2024-05-07]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0000343	OMIM:235830	TAS					P	HPO:skoehler[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0000431	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0002123	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0000407	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0000319	OMIM:235830	TAS					P	HPO:skoehler[2013-03-12]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0002927	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0005819	OMIM:235830	TAS					P	HPO:probinson[2013-04-13]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0000007	OMIM:235830	IEA					I	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0001800	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0000219	OMIM:235830	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0008666	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0000400	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0001249	OMIM:235830	IEA					P	HPO:iea[2009-02-17]
OMIM:235830	Histidinuria due to A renal tubular defect		HP:0005844	OMIM:235830	TAS					P	HPO:probinson[2013-04-13]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001276	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0000252	OMIM:615917	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001321	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0002079	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0000590	PMID:25058219	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0012707	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001263	OMIM:615917	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001252	PMID:25058219	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001251	PMID:25058219	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0003593	PMID:25058219	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0030682	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0010851	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0011923	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0002093	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001639	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001518	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0000508	PMID:25058219	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0000007	PMID:25058219	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0008347	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0001324	PMID:25058219	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0007359	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0003348	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0003128	PMID:27502409	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:615917	Combined oxidative phosphorylation deficiency 20		HP:0003623	PMID:27502409	PCS		1/1			C	HPO:probinson[2022-11-08]
OMIM:603813	Hypercholesterolemia, autosomal recessive		HP:0002155	PMID:12016260	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-26]
OMIM:603813	Hypercholesterolemia, autosomal recessive		HP:0003563	PMID:12016260	PCS		3/3			P	HPO:probinson[2023-03-26]
OMIM:603813	Hypercholesterolemia, autosomal recessive		HP:0003124	PMID:12016260	PCS		3/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-03-26]
OMIM:603813	Hypercholesterolemia, autosomal recessive		HP:0010874	PMID:12016260	PCS		3/3			P	HPO:skoehler[2013-01-14];HPO:probinson[2023-03-26]
OMIM:603813	Hypercholesterolemia, autosomal recessive		HP:0000007	PMID:12016260	PCS					I	HPO:skoehler[2013-01-14];HPO:probinson[2023-03-26]
OMIM:603813	Hypercholesterolemia, autosomal recessive		HP:0002621	OMIM:603813	IEA					P	HPO:skoehler[2013-01-14]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000252	PMID:35395208	PCS		2/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000483	PMID:35395208	PCS		1/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000750	PMID:35395208	PCS		1/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000486	PMID:35395208	PCS		5/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0002376	PMID:35395208	PCS		1/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0001250	PMID:35395208	PCS		8/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0011968	PMID:35395208	PCS		16/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0001252	PMID:35395208	PCS		22/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0001263	PMID:35395208	PCS		30/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0001251	PMID:35395208	PCS		2/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0002020	PMID:35395208	PCS		7/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0012443	PMID:35395208	PCS		13/17			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0100704	PMID:35395208	PCS		1/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0001328	PMID:35395208	PCS		2/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0008751	PMID:35395208	PCS		1/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0006532	PMID:35395208	PCS		3/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000256	PMID:35395208	PCS		10/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000410	PMID:35395208	PCS		2/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0002019	PMID:35395208	PCS		16/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000006	PMID:35395208	PCS					I	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0001249	PMID:35395208	PCS		30/35			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0000028	PMID:35395208	PCS		5/26			P	HPO:probinson[2022-09-04]
OMIM:620012	Developmental delay, hypotonia, and impaired language		HP:0001875	PMID:35395208	PCS		2/35			P	HPO:probinson[2022-09-04]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0004432	PMID:30718914	PCS		6/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0001508	PMID:30718914	PCS		2/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0011463	PMID:30718914	PCS		2/6			C	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0001051	PMID:30718914	PCS		1/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0000407	PMID:30718914	PCS		1/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0003593	PMID:30718914	PCS		1/6			C	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0002718	PMID:30718914	PCS		6/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0030252	PMID:30718914	PCS		6/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0000007	PMID:30718914	PCS					I	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0000964	PMID:30718914	PCS		2/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0001873	PMID:30718914	PCS		2/6			P	HPO:probinson[2022-03-18]
OMIM:619693	Agammaglobulinemia 9, autosomal recessive		HP:0003623	PMID:30718914	PCS		3/6			C	HPO:probinson[2022-03-18]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000286	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0002983	PMID:28400947	PCS	HP:0011461	2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0001156	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0005257	PMID:28400947	PCS	HP:0011461	2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0005474	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0003031	PMID:28400947	PCS	HP:0011461	2/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0003175	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0004719	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000316	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000954	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000238	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000219	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0002119	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000476	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000113	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000773	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0004691	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0002190	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0100259	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0100258	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000926	PMID:28400947	PCS	HP:0011461	2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0008422	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000921	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000007	PMID:28400947	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000268	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0002986	PMID:28400947	PCS	HP:0011461	2/2			P	HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0000347	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-06]
OMIM:617866	Short-Rib thoracic dysplasia 18 with polydactyly		HP:0002566	PMID:28400947	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003202	OMIM:310440	TAS					P	HPO:skoehler[2013-01-22]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003236	OMIM:310440	IEA					P	HPO:iea[2009-02-17]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0002650	OMIM:310440	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0002486	OMIM:310440	IEA					P	HPO:skoehler[2010-06-20]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0001371	OMIM:310440	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003198	OMIM:310440	TAS					P	HPO:probinson[2009-02-17]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003551	OMIM:310440	IEA					P	HPO:iea[2009-02-17]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0001270	OMIM:310440	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003391	OMIM:310440	TAS					P	HPO:skoehler[2015-12-30]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0002093	OMIM:310440	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0011463	PMID:23315026	PCS		45/45			C	HPO:probinson[2023-02-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0001419	PMID:23315026	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0009046	OMIM:310440	TAS					P	HPO:skoehler[2012-10-17]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003829	OMIM:310440	TAS					I	HPO:skoehler[2013-01-22]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0001319	OMIM:310440	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0001626	PMID:23315026	PCS		0/45			P	HPO:probinson[2012-07-26];HPO:probinson[2023-02-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0007941	OMIM:310440	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0025717	PMID:23315026	PCS		14/14			P	HPO:probinson[2023-02-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003713	PMID:23315026	PCS		0/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0001249	PMID:23315026	PCS		0/45			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0008956	PMID:23315026	PCS		45/45			P	HPO:probinson[2023-02-06]
OMIM:310440	Myopathy, X-linked, with excessive autophagy		HP:0003677	OMIM:310440	IEA					C	HPO:iea[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0000572	OMIM:300653	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0003621	PMID:1547346	PCS		1/1			C	HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0000750	OMIM:300653	IEA					P	HPO:iea[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0003201	OMIM:300653	IEA					P	HPO:iea[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001250	OMIM:300653	IEA					P	HPO:iea[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0003198	OMIM:300653	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0002076	OMIM:300653	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0000083	OMIM:300653	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001263	PMID:1547346	PCS		0/1			P	HPO:iea[2012-06-03];HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001251	OMIM:300653	IEA					P	HPO:iea[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0012132	PMID:1547346	PCS		1/1			P	HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001419	PMID:6933565	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001878	PMID:1547346	PCS		1/1			P	HPO:probinson[2012-05-06];HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0000712	OMIM:300653	IEA					P	HPO:iea[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001923	OMIM:300653	IEA					P	HPO:iea[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001324	PMID:1547346	PCS		1/1			P	HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0008305	OMIM:300653	TAS					P	HPO:probinson[2012-05-06]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0000556	OMIM:300653	IEA		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0001249	PMID:16567715;PMID:1547346	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11];HPO:probinson[2022-09-11];HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0003710	PMID:16567715	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-11]
OMIM:300653	Phosphoglycerate kinase 1 deficiency		HP:0003546	OMIM:300653	IEA					P	HPO:iea[2009-02-17]
OMIM:619687	Dystonia 33		HP:0008936	PMID:33236446	PCS		1/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0003621	PMID:33236446	PCS		4/11			C	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0001332	PMID:33236446	PCS		12/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0002530	PMID:33236446	PCS		3/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0003487	PMID:33236446	PCS		3/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0001761	PMID:33236446	PCS		1/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0002451	PMID:33236446	PCS		9/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0032807	PMID:33236446	PCS	HP:0003623	1/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0001263	PMID:33236446	PCS		2/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0025708	PMID:33236446	PCS		1/11			C	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0011463	PMID:33236446	PCS		6/11			C	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0001257	PMID:33236446	PCS		2/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0000006	PMID:33236446	PCS					I	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0001249	PMID:33236446	PCS		1/12			P	HPO:probinson[2022-03-08]
OMIM:619687	Dystonia 33		HP:0000511	PMID:33236446	PCS		1/12			P	HPO:probinson[2022-03-08]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0001397	PMID:25556185	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0001399	PMID:25556185	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0002013	PMID:25556185	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0002151	PMID:25556185	PCS		2/2			P	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0003593	PMID:25556185	PCS		1/2			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0002240	PMID:25556185	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0000815	PMID:25556185	PCS		1/2			P	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0001508	PMID:25556185	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0011463	PMID:25556185	PCS		1/2			C	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0001943	PMID:25556185	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0002925	PMID:25556185	PCS		1/2			P	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0000007	PMID:25556185	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0001945	PMID:25556185	PCS		1/2			P	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0001876	PMID:25556185	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0003138	PMID:25556185	PCS		1/2			P	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0003259	PMID:25556185	PCS		1/2			P	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0008527	PMID:25556185	PCS		2/2			P	HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0008207	PMID:25556185	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617872	Combined oxidative phosphorylation deficiency 34		HP:0003128	PMID:25556185	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:271900	Canavan disease		HP:0002069	PMID:34446995	PCS		5/12			P	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0002521	PMID:34446995	PCS		1/5			P	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0001476	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:271900	Canavan disease		HP:0000365	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:271900	Canavan disease		HP:0001252	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:271900	Canavan disease		HP:0003593	PMID:34446995	PCS		12/12			C	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:6000354	PMID:8252036	PCS		22/22			P	HPO:probinson[2024-02-27]
OMIM:271900	Canavan disease		HP:0010841	PMID:34446995	PCS		2/5			P	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0012444	OMIM:271900	TAS					P	HPO:skoehler[2013-11-28]
OMIM:271900	Canavan disease		HP:0000639	PMID:34446995	PCS		6/12			P	HPO:probinson[2012-04-11];HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0000618	PMID:34446995	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0000256	PMID:34446995	PCS		7/12			P	HPO:probinson[2012-04-11];HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0007305	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:271900	Canavan disease		HP:0002179	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:271900	Canavan disease		HP:0000252	PMID:34446995	PCS		2/12			P	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0002376	OMIM:264470	PCS					P	HPO:probinson[2012-04-11]
OMIM:271900	Canavan disease		HP:0025053	PMID:34446995	PCS		10/10			P	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0001263	PMID:34446995	PCS		12/12			P	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0034649	PMID:34446995	PCS		6/8			P	HPO:probinson[2019-04-20];HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0011097	PMID:34446995	PCS		1/12			P	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0032273	OMIM:271900	TAS					P	HPO:probinson[2019-04-20]
OMIM:271900	Canavan disease		HP:0032274	OMIM:271900	TAS					P	HPO:probinson[2019-04-20]
OMIM:271900	Canavan disease		HP:0000007	OMIM:264470	PCS					I	HPO:probinson[2012-04-11]
OMIM:271900	Canavan disease		HP:0007256	PMID:34446995	PCS		12/12			P	HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0000648	PMID:34446995	PCS		4/12			P	HPO:probinson[2012-04-11];HPO:probinson[2022-04-30]
OMIM:271900	Canavan disease		HP:0000505	PMID:34446995	PCS		12/12			P	HPO:probinson[2022-04-30]
OMIM:206550	Angiolipomatosis, familial		HP:0011462	OMIM:206550	TAS					C	HPO:probinson[2009-02-17]
OMIM:206550	Angiolipomatosis, familial		HP:0000007	OMIM:206550	TAS					I	HPO:probinson[2009-02-17]
OMIM:206550	Angiolipomatosis, familial		HP:0006773	OMIM:206550	TAS					P	HPO:probinson[2009-02-17]
OMIM:182830	Spastic paraplegia, optic atrophy, and dementia		HP:0001133	OMIM:182830	IEA					P	HPO:iea[2009-02-17]
OMIM:182830	Spastic paraplegia, optic atrophy, and dementia		HP:0000726	OMIM:182830	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182830	Spastic paraplegia, optic atrophy, and dementia		HP:0000648	OMIM:182830	IEA					P	HPO:iea[2009-02-17]
OMIM:182830	Spastic paraplegia, optic atrophy, and dementia		HP:0000543	OMIM:182830	IEA					P	HPO:iea[2009-02-17]
OMIM:182830	Spastic paraplegia, optic atrophy, and dementia		HP:0001258	OMIM:182830	IEA					P	HPO:iea[2009-02-17]
OMIM:182830	Spastic paraplegia, optic atrophy, and dementia		HP:0000006	OMIM:182830	IEA					I	HPO:iea[2009-02-17]
OMIM:613382	Brachydactyly, type E2		HP:0000684	OMIM:613382	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613382	Brachydactyly, type E2		HP:0004322	OMIM:613382	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613382	Brachydactyly, type E2		HP:0001156	OMIM:613382	IEA					P	HPO:skoehler[2015-01-19]
OMIM:613382	Brachydactyly, type E2		HP:0010049	OMIM:613382	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613382	Brachydactyly, type E2		HP:0000006	OMIM:613382	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613382	Brachydactyly, type E2		HP:0000677	OMIM:613382	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613382	Brachydactyly, type E2		HP:0010743	OMIM:613382	IEA					P	HPO:skoehler[2010-06-19]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001397	OMIM:255120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001254	PMID:9691089	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0003236	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0002686	OMIM:255120	IEA					H	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001250	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001252	PMID:9691089	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0002240	PMID:9691089	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001290	OMIM:255120	TAS					P	HPO:skoehler[2017-07-13]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0011675	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001270	PMID:9691089	PCS		1/1			P	HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0031964	PMID:9691089	PCS		1/1			P	HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0002919	PMID:9691089	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001947	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0011463	PMID:9691089	PCS		1/1			C	HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0008279	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001987	OMIM:255120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001324	PMID:9691089	PCS		0/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-09]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0002910	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001985	PMID:9691089	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0002014	PMID:9691089	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001265	PMID:9691089	PCS		1/1			P	HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0031956	PMID:9691089	PCS		1/1			P	HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001640	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0011968	PMID:9691089	PCS		1/1			P	HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0000007	PMID:9691089	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0007335	PMID:9691089	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0003215	PMID:9691089	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-18]
OMIM:255120	Carnitine palmitoyltransferase I deficiency		HP:0001259	OMIM:255120	IEA					P	HPO:iea[2009-02-17]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0002245	PMID:37710961	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000286	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0001770	PMID:37710961;PMID:30573562	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0003577	PMID:37710961;PMID:30573562	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0001355	PMID:37710961;PMID:30573562	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000343	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000321	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000463	PMID:37710961;PMID:30573562	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0003196	PMID:37710961	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0001270	PMID:37710961;PMID:30573562	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0001629	PMID:37710961;PMID:30573562	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0011220	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000316	PMID:37710961;PMID:30573562	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000238	PMID:37710961;PMID:30573562	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0002119	PMID:37710961;PMID:30573562	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0002779	PMID:37710961;PMID:30573562	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0008897	PMID:37710961;PMID:30573562	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000218	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000278	PMID:37710961	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0003006	PMID:37710961;PMID:30573562	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0001249	PMID:37710961;PMID:30573562	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000358	PMID:37710961;PMID:30573562	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0032407	PMID:37710961;PMID:30573562	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000574	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000431	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0002079	PMID:37710961;PMID:30573562	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0002197	PMID:37710961;PMID:30573562	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0002098	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0001263	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0005280	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0012810	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0100259	PMID:37710961;PMID:30573562	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0009110	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0005819	PMID:37710961;PMID:30573562	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0011230	PMID:30573562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0001999	PMID:37710961	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000369	PMID:37710961;PMID:30573562	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000006	PMID:30573562	PCS					I	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0002589	PMID:37710961;PMID:30573562	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:620748	Megalencephaly-polydactyly syndrome		HP:0000126	PMID:37710961	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-15]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0002421	PMID:33397746	PCS		4/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0001276	PMID:33397746	PCS		4/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0002069	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000340	PMID:33397746	PCS		4/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000582	PMID:33397746	PCS		3/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0002521	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000365	PMID:33397746	PCS		2/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0002540	PMID:33397746	PCS		3/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0002188	PMID:33397746	PCS		3/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0003593	PMID:33397746	PCS		1/5			C	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0032794	PMID:33397746	PCS		3/5			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0033725	PMID:33397746	PCS		3/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000518	PMID:33397746	PCS		5/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0011461	PMID:33397746	PCS		4/5			C	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000316	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000733	PMID:33397746	PCS		1/3			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000219	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000154	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0008936	PMID:33397746	PCS		5/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000252	PMID:33397746	PCS		5/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0012736	PMID:33397746	PCS		5/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0011097	PMID:33397746	PCS		2/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000826	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000426	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000007	PMID:33397746	PCS					I	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000307	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000400	PMID:33397746	PCS		4/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0000687	PMID:33397746	PCS		1/5			P	HPO:probinson[2022-08-13]
OMIM:619877	Dentici-Novelli neurodevelopmental syndrome		HP:0009879	PMID:33397746	PCS		3/5			P	HPO:probinson[2022-08-13]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0002013	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0002153	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0000848	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0001508	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0001944	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0002902	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0000007	OMIM:203400	IEA					I	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0001954	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0008872	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0004319	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0002615	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0001510	OMIM:203400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0000127	OMIM:203400	IEA					P	HPO:iea[2009-02-17]
OMIM:203400	Corticosterone methyloxidase type I deficiency		HP:0003623	OMIM:203400	IEA					C	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0000121	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0003126	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0005576	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0000083	OMIM:310468	TAS	HP:0003581				P	HPO:probinson[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0001419	PMID:8559248	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-03-12]
OMIM:310468	Nephrolithiasis, type I		HP:0002907	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0000096	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0002150	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0000092	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0000114	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0000787	OMIM:310468	IEA					P	HPO:iea[2009-02-17]
OMIM:310468	Nephrolithiasis, type I		HP:0012622	OMIM:310468	TAS					P	HPO:probinson[2014-01-18]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000494	PMID:28866611	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0001212	PMID:28866611	PCS		2/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0010648	PMID:28866611	PCS		3/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0001250	PMID:28866611	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0001263	PMID:28866611	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0001252	PMID:28866611	PCS		5/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0003593	PMID:28866611	PCS		5/5			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0011800	PMID:28866611	PCS		3/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0011229	PMID:28866611	PCS		2/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000629	PMID:28866611	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0011098	PMID:28866611	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000717	PMID:28866611	PCS		3/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000733	PMID:28866611	PCS		3/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000307	PMID:28866611	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0008897	PMID:28866611	PCS		2/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000527	PMID:28866611	PCS		1/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0007874	PMID:28866611	PCS		2/5			P	HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0002007	PMID:28866611	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000256	PMID:28866611	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0000006	PMID:28866611	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0001249	PMID:28866611	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617682	Pilarowski-Bjornsson syndrome		HP:0002721	PMID:28866611	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0001276	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0002059	PMID:23178126	PCS				HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0003577	PMID:23178126	PCS		9/9			C	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0000340	PMID:23178126	PCS					P	HPO:skoehler[2013-06-12];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0000453	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0002188	PMID:23178126	PCS					P	HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0001272	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0001274	PMID:23178126	PCS					P	HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0002171	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0011344	PMID:23178126	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0034295	PMID:23178126	PCS					P	HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0000518	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0100307	PMID:23178126	PCS					P	HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0001518	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0011451	PMID:23178126	PCS	HP:0003577	9/9		HP:0012828	P	HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0000426	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0002804	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0000007	PMID:23178126	PCS					I	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0001511	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0001257	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0000347	PMID:23178126	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-10-08]
OMIM:615095	Microcephaly 10, primary, autosomal recessive		HP:0009879	PMID:23178126	PCS					P	HPO:probinson[2022-10-08]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0003621	PMID:14615110	PCS		1/2			C	HPO:probinson[2022-09-06]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0005575	PMID:14615110	PCS		2/2			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-09-06]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0005421	PMID:14615110	PCS		1/2			P	HPO:probinson[2022-09-06]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0000790	OMIM:612922	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0000093	OMIM:612922	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0001919	PMID:14615110	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-06]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0001937	PMID:14615110	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-06]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0001903	OMIM:612922	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0011463	PMID:14615110	PCS		1/2			C	HPO:probinson[2022-09-06]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0000822	OMIM:612922	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0000007	OMIM:612922	TAS					I	HPO:skoehler[2012-10-17]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0100519	OMIM:612922	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0001873	OMIM:612922	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0000006	PMID:14615110	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-06]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0003138	OMIM:612922	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612922	Hemolytic uremic syndrome, atypical, susceptibility to, 2		HP:0003259	OMIM:612922	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615081	Spermatogenic failure 11		HP:0003251	PMID:17047026	PCS		7/7			P	HPO:probinson[2021-10-03]
OMIM:615081	Spermatogenic failure 11		HP:0012207	PMID:17047026	PCS		4/7			P	HPO:probinson[2021-10-03]
OMIM:615081	Spermatogenic failure 11		HP:0000006	PMID:17047026	PCS					I	HPO:skoehler[2013-03-08];HPO:probinson[2021-10-03]
OMIM:615081	Spermatogenic failure 11		HP:0000798	PMID:17047026	PCS		7/7			P	HPO:probinson[2021-10-03]
OMIM:615081	Spermatogenic failure 11		HP:0012864	PMID:17047026	PCS		5/7			P	HPO:probinson[2021-10-03]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000341	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0003577	PMID:19559397	PCS		5/5			C	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000486	OMIM:612936	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0002200	OMIM:612936	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001272	OMIM:612936	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001250	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001252	PMID:19559397	PCS		5/5			P	HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001251	PMID:19559397	PCS		0/5			P	HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000280	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000414	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0002119	PMID:19559397	PCS		3/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000218	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001347	PMID:19559397	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000154	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000252	OMIM:612936	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0002510	PMID:19559397	PCS		5/5			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001762	PMID:19559397	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0003487	PMID:19559397	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0002079	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001263	PMID:19559397	PCS		5/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0002171	OMIM:612936	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0012811	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0100021	PMID:19559397	PCS		5/5			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001181	PMID:19559397	PCS		4/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0033683	PMID:19559397	PCS		4/4			P	HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0002509	PMID:19559397	PCS		4/4			P	HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000007	PMID:19559397	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0001319	OMIM:612936	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0002307	PMID:19559397	PCS		3/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000543	PMID:19559397	PCS		1/5			P	HPO:probinson[2023-03-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000322	OMIM:612936	TAS					P	HPO:skoehler[2015-10-16]
OMIM:612936	Spastic paraplegia 50, autosomal recessive		HP:0000303	OMIM:612936	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002300	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:6001187	PMID:29053785	PCS					P	HPO:probinson[2025-09-26]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002145	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002120	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002186	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002185	OMIM:607485	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002381	OMIM:607485	TAS		20/20			P	HPO:probinson[2013-08-13];HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0000738	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0007064	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0000734	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0000713	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0000751	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0000710	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0006956	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0001300	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002354	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:5200321	OMIM:607485	TAS					P	HPO:skoehler[2015-01-04]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0030223	OMIM:607485	TAS					P	HPO:skoehler[2015-01-04]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002591	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002171	OMIM:607485	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0100315	OMIM:607485	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0002529	OMIM:607485	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0008762	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0000741	OMIM:607485	IEA					P	HPO:iea[2009-02-17]
OMIM:607485	Frontotemporal lobar degeneration with TDP43 inclusions		HP:0000006	OMIM:607485	IEA					I	HPO:iea[2009-02-17]
OMIM:606943	Usher syndrome, type IG		HP:0001751	OMIM:606943	IEA					P	HPO:iea[2009-02-17]
OMIM:606943	Usher syndrome, type IG		HP:0000407	OMIM:606943	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606943	Usher syndrome, type IG		HP:0000007	OMIM:606943	IEA					I	HPO:iea[2009-02-17]
OMIM:606943	Usher syndrome, type IG		HP:0000510	OMIM:606943	IEA					P	HPO:iea[2009-02-17]
OMIM:606943	Usher syndrome, type IG		HP:0004646	OMIM:606943	IEA					P	HPO:iea[2009-02-17]
OMIM:130700	Emphysema, hereditary pulmonary		HP:0002097	OMIM:130700	IEA					P	HPO:iea[2009-02-17]
OMIM:130700	Emphysema, hereditary pulmonary		HP:0006510	OMIM:130700	IEA					P	HPO:iea[2009-02-17]
OMIM:130700	Emphysema, hereditary pulmonary		HP:0004469	OMIM:130700	IEA					P	HPO:iea[2009-02-17]
OMIM:179300	Radioulnar synostosis		HP:0006394	OMIM:179300	TAS					P	HPO:probinson[2022-08-24];HPO:probinson[2022-08-24]
OMIM:179300	Radioulnar synostosis		HP:0000006	PMID:31138930	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-24]
OMIM:179300	Radioulnar synostosis		HP:0002974	PMID:31138930	PCS		22/22			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-24]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0000362	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0000365	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0002650	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0003321	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0005005	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0004322	OMIM:166220	TAS	HP:0003593				P	HPO:probinson[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0003023	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0000592	OMIM:166220	TAS					P	HPO:skoehler[2010-06-20];HPO:probinson[2024-08-03]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:6000871	PMID:18798308	PCS		2/20			P	HPO:probinson[2024-08-03]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0002808	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0000703	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0002757	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0002659	OMIM:166220	TAS					P	HPO:probinson[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0002645	OMIM:166220	TAS					P	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0000006	OMIM:166220	TAS					I	HPO:iea[2009-02-17]
OMIM:166220	Osteogenesis imperfecta, type IV		HP:0004349	PMID:19533842	PCS					P	HPO:probinson[2015-03-22]
OMIM:303400	Cleft palate, X-linked		HP:0000175	OMIM:303400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:303400	Cleft palate, X-linked		HP:0000193	OMIM:303400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:303400	Cleft palate, X-linked		HP:0010296	OMIM:303400	IEA					P	HPO:skoehler[2010-06-18]
OMIM:303400	Cleft palate, X-linked		HP:0001417	OMIM:303400	IEA					I	HPO:iea[2009-02-17]
OMIM:134200	Facial palsy, familial recurrent peripheral		HP:0010628	OMIM:134200	IEA					P	HPO:iea[2009-02-17]
OMIM:134200	Facial palsy, familial recurrent peripheral		HP:0000006	OMIM:134200	IEA					I	HPO:iea[2009-02-17]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0025175	PMID:25848748	PCS					P	HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0003581	PMID:25848748	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0032341	PMID:25848748	PCS		8/8			P	HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0003829	PMID:25848748	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0032342	PMID:25848748	PCS		5/8			P	HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0012735	PMID:25848748	PCS					P	HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0002216	PMID:25848748	PCS		HP:0040283			P	HPO:skoehler[2015-06-22];HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0002206	PMID:25848748	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0031413	PMID:25848748	PCS					P	HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0000006	PMID:25848748	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-05]
OMIM:616371	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4		HP:0045051	PMID:25848748	PCS		8/8			P	HPO:probinson[2020-10-05]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0002650	PMID:17101916;PMID:22462675	PCS		2/3			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0031936	PMID:17101916	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0004322	PMID:22462675	PCS		2/2			P	HPO:probinson[2020-11-30];HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0003693	PMID:17101916	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0003273	PMID:17101916	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0003593	PMID:17101916;PMID:22462675	PCS		3/3			C	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0002460	PMID:17101916	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0001284	PMID:17101916;PMID:22462675	PCS		3/3			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0001290	PMID:22462675	PCS		2/2			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0001270	PMID:22462675	PCS		2/2			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0002093	PMID:17101916	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0010546	PMID:22462675	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0007340	PMID:17101916	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0002938	PMID:17101916;PMID:22462675	PCS		3/3			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0003803	PMID:22462675	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0001621	PMID:17101916	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0001324	PMID:22462675	PCS		2/2			P	HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0000006	PMID:17101916	PCS					I	HPO:probinson[2020-11-30];HPO:probinson[2020-11-30]
OMIM:619042	Spinal muscular atrophy, infantile, James type		HP:0003557	PMID:22462675	PCS		1/1			P	HPO:probinson[2020-11-30]
OMIM:600513	Epilepsy, nocturnal frontal lobe, type 1		HP:0001250	PMID:7895015	PCS	HP:0011463				P	HPO:iea[2009-02-17]
OMIM:600513	Epilepsy, nocturnal frontal lobe, type 1		HP:0011463	PMID:7895015	PCS					C	HPO:probinson[2017-06-14]
OMIM:600513	Epilepsy, nocturnal frontal lobe, type 1		HP:0003829	OMIM:600513	TAS					I	HPO:skoehler[2013-01-21]
OMIM:600513	Epilepsy, nocturnal frontal lobe, type 1		HP:0007359	PMID:7895015	PCS					P	HPO:probinson[2009-02-17]
OMIM:600513	Epilepsy, nocturnal frontal lobe, type 1		HP:0000006	PMID:7895015	PCS					I	HPO:iea[2009-02-17]
OMIM:600513	Epilepsy, nocturnal frontal lobe, type 1		HP:0001249	PMID:14623738	PCS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0002069	PMID:28236339	PCS	HP:0003593	4/4			P	HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0000252	PMID:28236339	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0000718	PMID:28236339	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0001263	PMID:28236339	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0001251	PMID:28236339	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0003593	PMID:28236339	PCS		4/4			C	HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0000007	PMID:28236339	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0001324	PMID:28236339	PCS	HP:0003621	4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0001533	PMID:28236339	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-21]
OMIM:617709	Neurodevelopmental disorder with microcephaly, ataxia, and seizures		HP:0001763	PMID:28236339	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-21]
OMIM:608629	Joubert syndrome 3		HP:0000286	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0003774	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0000463	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0001252	PMID:15467982	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0001251	PMID:15467982	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0000580	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0011933	OMIM:608629	TAS					P	HPO:probinson[2012-06-10]
OMIM:608629	Joubert syndrome 3		HP:0001270	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0033725	PMID:15322546	PCS		3/4			P	HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0000639	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0000657	PMID:15467982	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0002419	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0002876	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0000512	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0001249	PMID:15467982	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0000556	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0001320	PMID:15467982	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0002553	OMIM:608629	TAS					P	HPO:probinson[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0006956	PMID:15322546	PCS		1/4			P	HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0000431	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0002871	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0031936	OMIM:608629	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608629	Joubert syndrome 3		HP:0000194	OMIM:608629	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608629	Joubert syndrome 3		HP:0002790	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0000090	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0100951	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0000508	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0000007	PMID:15322546	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-03]
OMIM:608629	Joubert syndrome 3		HP:0000505	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0001631	PMID:15322546	PCS	HP:0003577	1/4			P	HPO:probinson[2022-09-02]
OMIM:608629	Joubert syndrome 3		HP:0000369	OMIM:608629	IEA					P	HPO:iea[2009-02-17]
OMIM:608629	Joubert syndrome 3		HP:0006821	PMID:15322546	PCS		3/4			P	HPO:probinson[2022-09-02]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0002465	PMID:24115387	PCS		4/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0000486	PMID:24115387	PCS		4/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0000276	PMID:24115387	PCS		4/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0001250	PMID:24115387	PCS		3/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0001263	PMID:24115387	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0003593	PMID:24115387	PCS					C	HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0001419	PMID:24115387	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0000648	PMID:24115387	PCS		1/6			P	HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0030084	PMID:24115387	PCS		1/6			P	HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0007687	PMID:24115387	PCS		1/6			P	HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0000400	PMID:24115387	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0000752	PMID:24115387	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0000322	PMID:24115387	PCS		1/6			P	HPO:probinson[2021-09-26]
OMIM:300928	Intellectual developmental disorder, X-linked 101		HP:0001249	PMID:24115387	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:108300	Stickler syndrome, type I		HP:0000541	PMID:8434604	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000463	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0000518	PMID:12544472	PCS		10/25			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0010891	PMID:16152640	PCS		9/22			P	HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0031153	PMID:11007540	PCS					P	HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0000618	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0006499	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0002758	PMID:16152640	PCS		18/22			P	HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0002655	OMIM:108300	IEA				HP:0012825	P	HPO:skoehler[2012-10-12]
OMIM:108300	Stickler syndrome, type I		HP:0001369	PMID:12544472	PCS		15/25			P	HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0001166	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0000176	PMID:16152640	PCS		6/22			P	HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0000175	PMID:8434604;PMID:12544472	PCS		8/28			P	HPO:probinson[2022-05-30];HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0003302	PMID:16152640	PCS		4/22			P	HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0002650	PMID:16152640	PCS		8/22			P	HPO:iea[2009-02-17];HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0001387	PMID:8434604	PCS		3/3			P	HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0001382	PMID:12544472	PCS		13/25			P	HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000193	PMID:16152640;PMID:12544472	PCS		11/47			P	HPO:probinson[2019-07-06];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000272	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0003040	PMID:8434604	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0011800	PMID:12544472	PCS		18/25			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0005280	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0002829	PMID:8434604	PCS		3/3			P	HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0001519	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0011530	PMID:12544472	PCS		17/25			P	HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0006361	OMIM:108300	IEA					P	HPO:skoehler[2012-10-12]
OMIM:108300	Stickler syndrome, type I		HP:0002808	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0000407	PMID:12544472	PCS		19/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000926	OMIM:108300	TAS					P	HPO:probinson[2013-04-14]
OMIM:108300	Stickler syndrome, type I		HP:0000767	OMIM:108300	IEA					P	HPO:iea[2009-02-17]
OMIM:108300	Stickler syndrome, type I		HP:0007773	PMID:12544472	PCS		25/25			P	HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000405	PMID:16152640	PCS		HP:0040283			P	HPO:skoehler[2010-06-20];HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0000201	PMID:12544472	PCS		2/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000006	PMID:16152640	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-07-06]
OMIM:108300	Stickler syndrome, type I		HP:0000501	PMID:12544472	PCS		2/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0001634	PMID:12544472	PCS		1/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000545	PMID:8434604;PMID:12544472	PCS		28/28			P	HPO:probinson[2022-05-30];HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0000347	PMID:12544472	PCS		15/25			P	HPO:probinson[2022-05-30]
OMIM:108300	Stickler syndrome, type I		HP:0004568	OMIM:108300	TAS					P	HPO:probinson[2013-04-14]
OMIM:619724	Dystonia 34, myoclonic		HP:0000473	PMID:32212350	PCS		2/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0001583	PMID:32212350	PCS		2/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0002378	PMID:32212350	PCS		5/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0003621	PMID:32212350	PCS		5/5			C	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0002356	PMID:32212350	PCS		2/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0001332	PMID:32212350	PCS		5/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0031629	PMID:32212350	PCS		2/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0000508	PMID:32212350	PCS		1/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0000646	PMID:32212350	PCS		1/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0007772	PMID:32212350	PCS		3/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0009921	PMID:32212350	PCS	HP:0003577	1/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0000006	PMID:32212350	PCS					I	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0002346	PMID:32212350	PCS		2/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0007338	PMID:32212350	PCS		1/5			P	HPO:probinson[2022-02-23]
OMIM:619724	Dystonia 34, myoclonic		HP:0001336	PMID:32212350	PCS		2/5			P	HPO:probinson[2022-02-23]
OMIM:145200	Hyperpigmentation of fuldauer and kuijpers		HP:0000953	OMIM:145200	TAS					P	HPO:probinson[2009-02-17]
OMIM:145200	Hyperpigmentation of fuldauer and kuijpers		HP:0000006	OMIM:145200	IEA					I	HPO:iea[2009-02-17]
DECIPHER:62	1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders)		HP:0000252	DECIPHER:62	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:62	1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders)		HP:0001249	DECIPHER:62	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614200	Bleeding disorder, platelet-type, 9		HP:0003577	OMIM:614200	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614200	Bleeding disorder, platelet-type, 9		HP:0000978	OMIM:614200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614200	Bleeding disorder, platelet-type, 9		HP:0001873	OMIM:614200	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:614200	Bleeding disorder, platelet-type, 9		HP:0000006	OMIM:614200	TAS					I	HPO:skoehler[2012-10-17]
DECIPHER:76	12q14 microdeletion syndrome		HP:0010739	DECIPHER:76	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:76	12q14 microdeletion syndrome		HP:0003508	DECIPHER:76	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:76	12q14 microdeletion syndrome		HP:0001249	DECIPHER:76	IEA					P	HPO:skoehler[2013-05-29]
OMIM:276100	Tryptophanuria with dwarfism		HP:0003510	OMIM:276100	IEA					P	HPO:iea[2009-02-17]
OMIM:276100	Tryptophanuria with dwarfism		HP:0000992	OMIM:276100	IEA					P	HPO:iea[2009-02-17]
OMIM:276100	Tryptophanuria with dwarfism		HP:0001288	OMIM:276100	IEA					P	HPO:iea[2009-02-17]
OMIM:276100	Tryptophanuria with dwarfism		HP:0003361	OMIM:276100	IEA					P	HPO:iea[2009-02-17]
OMIM:276100	Tryptophanuria with dwarfism		HP:0001251	OMIM:276100	IEA					P	HPO:iea[2009-02-17]
OMIM:276100	Tryptophanuria with dwarfism		HP:0000007	OMIM:276100	IEA					I	HPO:iea[2009-02-17]
OMIM:276100	Tryptophanuria with dwarfism		HP:0000524	OMIM:276100	IEA					P	HPO:iea[2009-02-17]
OMIM:276100	Tryptophanuria with dwarfism		HP:0001249	OMIM:276100	IEA					P	HPO:iea[2009-02-17]
OMIM:148730	Keratosis, focal palmoplantar and gingival		HP:0008392	OMIM:148730	IEA					P	HPO:iea[2009-02-17]
OMIM:148730	Keratosis, focal palmoplantar and gingival		HP:0000222	OMIM:148730	IEA					P	HPO:iea[2009-02-17]
OMIM:148730	Keratosis, focal palmoplantar and gingival		HP:0007497	OMIM:148730	IEA					P	HPO:iea[2009-02-17]
OMIM:148730	Keratosis, focal palmoplantar and gingival		HP:0008399	OMIM:148730	IEA					P	HPO:iea[2009-02-17]
OMIM:148730	Keratosis, focal palmoplantar and gingival		HP:0000006	OMIM:148730	IEA					I	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0003577	PMID:32160409	PCS		1/1			C	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001981	PMID:32160409	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001530	OMIM:224120	IEA					P	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0005532	OMIM:224120	IEA					P	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0003352	OMIM:224120	IEA					P	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0002240	PMID:32160409	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0010972	OMIM:224120	IEA					P	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0012132	PMID:32160409	PCS		1/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0011273	OMIM:224120	TAS					P	HPO:skoehler[2014-04-13]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001518	PMID:32160409	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0002904	PMID:32160409	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001878	PMID:32160409	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001789	OMIM:224120	IEA					P	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0020122	PMID:32160409	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0000007	PMID:12434312	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001923	OMIM:224120	TAS					P	HPO:skoehler[2014-04-13]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0025435	PMID:32160409	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001159	OMIM:224120	TAS		HP:0040283			P	HPO:skoehler[2014-04-13]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0001744	OMIM:224120	TAS					P	HPO:skoehler[2014-04-13]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0003655	OMIM:224120	IEA					P	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0006579	OMIM:224120	IEA					P	HPO:iea[2009-02-17]
OMIM:224120	Anemia, congenital dyserythropoietic, type Ia		HP:0004447	OMIM:224120	TAS					P	HPO:skoehler[2014-04-13]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000286	PMID:32346159	PCS		7/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000365	PMID:32346159	PCS		2/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0010803	PMID:32346159	PCS		5/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0004322	PMID:32346159	PCS		3/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000463	PMID:32346159	PCS		4/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001250	PMID:32346159	PCS		3/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0003593	PMID:32346159	PCS					C	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001290	PMID:32346159	PCS		9/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001270	PMID:32346159	PCS		13/14			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0002719	PMID:32346159	PCS		7/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0011463	PMID:32346159	PCS					C	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000718	PMID:32346159	PCS		5/14			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000739	PMID:32346159	PCS		4/14			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0012450	PMID:32346159	PCS		3/8			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0008551	PMID:32346159	PCS		3/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000316	PMID:32346159	PCS		6/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000736	PMID:32346159	PCS		5/14			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000256	PMID:32346159	PCS		3/13			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001249	PMID:32346159	PCS		5/6			P	HPO:probinson[2020-12-10];HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001562	PMID:32346159	PCS	HP:0011461	1/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000154	PMID:32346159	PCS		4/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001363	PMID:32346159	PCS		2/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000494	PMID:32346159	PCS		6/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000750	PMID:32346159	PCS		14/14			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001382	PMID:32346159	PCS		7/13			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0011968	PMID:32346159	PCS		3/8			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000293	PMID:32346159	PCS		2/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000490	PMID:32346159	PCS		4/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001263	PMID:32346159	PCS		14/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0100753	PMID:32346159	PCS		1/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000729	PMID:32346159	PCS		3/14			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000348	PMID:32346159	PCS		7/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000505	PMID:32346159	PCS		6/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000006	PMID:32346159	PCS					I	HPO:probinson[2020-12-10];HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0001513	PMID:32346159	PCS		3/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000369	PMID:32346159	PCS		4/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000445	PMID:32346159	PCS		6/15			P	HPO:probinson[2020-12-10]
OMIM:619056	Neurodevelopmental disorder with speech impairment and dysmorphic facies		HP:0000687	PMID:32346159	PCS		3/15			P	HPO:probinson[2020-12-10]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0000819	PMID:11372010	PCS	HP:0003623				P	HPO:iea[2009-02-17];HPO:probinson[2020-07-17]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0030795	PMID:14578306	PCS					P	HPO:probinson[2020-07-26]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0001518	PMID:14578306	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-07-26]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0003074	PMID:14578306	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-26]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0000007	PMID:11372010	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2020-07-17]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0001511	PMID:14578306	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-07-26]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0100651	PMID:14578306	PCS	HP:0003623	3/3			P	HPO:probinson[2020-07-26]
OMIM:606176	Diabetes mellitus, permanent neonatal 1		HP:0040217	PMID:14578306	PCS					P	HPO:probinson[2020-07-26]
OMIM:300082	Cognitive function 1, social		HP:0000707	OMIM:300082	IEA					P	HPO:iea[2009-02-17]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0003774	PMID:28117080;OMIM:618348	PCS		11/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000341	PMID:28280135	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000340	PMID:28280135	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0003676	OMIM:618348	IEA					C	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0004322	OMIM:618348	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000100	OMIM:618348	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0410030	OMIM:618348	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001629	OMIM:618348	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000319	PMID:28280135	PCS		4/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000954	PMID:28280135	PCS		2/5			P	HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001822	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000218	OMIM:618348	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001967	OMIM:618348	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0030084	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0009944	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001249	PMID:28280135	PCS		5/5			P	HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001644	OMIM:618348	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0002751	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001166	OMIM:618348	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000252	PMID:28280135;PMID:28117080	PCS		8/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000175	OMIM:618348	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0003621	PMID:28280135	PCS		3/3			C	HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000794	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000750	PMID:28280135	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0003124	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001263	PMID:28280135	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000097	PMID:28280135;PMID:28117080	PCS		3/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000093	PMID:28280135	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000092	OMIM:618348	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0012579	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000969	PMID:28280135	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000924	OMIM:618348	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000767	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0001999	OMIM:618348	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000007	OMIM:618348	IEA					I	HPO:skoehler[2019-04-18]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000964	PMID:28117080	PCS		2/3			P	HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0002967	PMID:28280135	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:618348	Galloway-Mowat syndrome 7		HP:0000347	PMID:28280135	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-10]
OMIM:601631	Anterior segment dysgenesis 3		HP:0001320	OMIM:601631	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:601631	Anterior segment dysgenesis 3		HP:0003577	PMID:12614756	PCS		1/4			C	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0003621	PMID:12614756	PCS		1/4			C	HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0007905	OMIM:601631	TAS	HP:0003621				P	HPO:probinson[2012-07-25]
OMIM:601631	Anterior segment dysgenesis 3		HP:0001492	PMID:12614756	PCS	HP:0003577	1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0009918	PMID:12614756	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0003593	PMID:12614756	PCS		1/4			C	HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0002280	OMIM:601631	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:601631	Anterior segment dysgenesis 3		HP:0000627	PMID:12614756	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0007990	PMID:12614756	PCS		2/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0011462	PMID:12614756	PCS		1/4			C	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0000558	OMIM:601631	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601631	Anterior segment dysgenesis 3		HP:0000659	PMID:12614756	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0000006	PMID:9620769	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-12]
OMIM:601631	Anterior segment dysgenesis 3		HP:0000501	PMID:12614756	PCS	HP:0003621	1/5			P	HPO:probinson[2012-07-25];HPO:probinson[2022-12-12]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0002344	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000365	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0001250	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0001670	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0002240	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000280	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0011463	PMID:11153910	PCS		8/16			C	HPO:probinson[2024-01-30]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000718	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0003309	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000752	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0002159	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0001007	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0001249	PMID:11153910	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-30]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0001744	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0002014	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0003621	PMID:11153910	PCS		8/16			C	HPO:iea[2009-02-17];HPO:probinson[2024-01-30]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:6000360	PMID:12202988	PCS		7/7			P	HPO:probinson[2024-02-27]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0001640	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0001387	OMIM:252920	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000250	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000943	PMID:11153910	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-30]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000007	PMID:11153910	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-01-30]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0002208	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000900	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0002788	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:252920	Mucopolysaccharidosis type IIIB		HP:0000664	OMIM:252920	IEA					P	HPO:iea[2009-02-17]
OMIM:156240	Mesothelioma, malignant		HP:0001442	OMIM:156240	TAS					I	HPO:skoehler[2017-07-13]
OMIM:156240	Mesothelioma, malignant		HP:0100001	OMIM:156240	IEA					P	HPO:skoehler[2009-02-17]
OMIM:618360	Brain small vessel disease 3		HP:0002059	PMID:30412317	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0002510	PMID:30412317	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0001250	PMID:30412317	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0002352	PMID:30412317	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0002132	PMID:30412317	PCS		1/2			P	HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0001263	PMID:30412317	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0001252	PMID:30412317	PCS		1/2			P	HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0003593	PMID:30412317	PCS		2/2			C	HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0000007	PMID:30412317	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0032325	PMID:30412317	PCS		1/2			P	HPO:probinson[2023-01-16]
OMIM:618360	Brain small vessel disease 3		HP:0002514	PMID:30412317	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:617053	Mirage syndrome		HP:0004325	PMID:27182967	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0004322	PMID:27182967	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0002043	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0001250	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0002020	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0003593	PMID:27182967	PCS		1/11			C	HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001270	PMID:27182967	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0011951	PMID:27182967	PCS		4/11		HP:0031796	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0006270	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0000815	PMID:27182967	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001903	PMID:27182967	PCS		9/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0010550	PMID:27182967	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0002718	PMID:27182967	PCS		10/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0100806	PMID:27182967	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000238	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001943	PMID:27182967	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001888	PMID:27182967	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000835	PMID:27182967	PCS		7/7			P	HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0030260	PMID:27182967	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0006433	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0008734	PMID:27182967	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001643	PMID:27182967	PCS		3/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0003623	PMID:27182967	PCS		10/11			C	HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000010	PMID:27182967	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0002650	PMID:27182967	PCS	HP:0003577	1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0001762	PMID:27182967	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001882	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0002571	PMID:27182967	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0002153	PMID:27182967	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001263	PMID:27182967	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0002170	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0010557	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001838	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13]
OMIM:617053	Mirage syndrome		HP:0002902	PMID:27182967	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000846	PMID:27182967	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000967	PMID:27182967	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001511	PMID:27182967	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000047	PMID:27182967	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0001873	PMID:27182967	PCS		11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000006	PMID:27182967	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000028	PMID:27182967	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0002863	PMID:27182967	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0002028	PMID:27182967	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:617053	Mirage syndrome		HP:0000049	PMID:27182967	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:309930	Muscular dystrophy, Cardiac type		HP:0003115	OMIM:309930	TAS					P	HPO:skoehler[2009-02-17]
OMIM:309930	Muscular dystrophy, Cardiac type		HP:0003236	OMIM:309930	IEA					P	HPO:iea[2009-02-17]
OMIM:309930	Muscular dystrophy, Cardiac type		HP:0003167	OMIM:309930	TAS					P	HPO:probinson[2009-02-17]
OMIM:309930	Muscular dystrophy, Cardiac type		HP:0003560	OMIM:309930	TAS					P	HPO:skoehler[2009-02-17]
OMIM:309930	Muscular dystrophy, Cardiac type		HP:0001638	OMIM:309930	IEA					P	HPO:iea[2009-02-17]
OMIM:309930	Muscular dystrophy, Cardiac type		HP:0001417	OMIM:309930	IEA					I	HPO:iea[2009-02-17]
OMIM:613235	Factor XIIIB deficiency		HP:0001892	PMID:8324218	PCS		1/1			P	HPO:probinson[2013-12-15];HPO:probinson[2022-09-25]
OMIM:613235	Factor XIIIB deficiency		HP:0003577	OMIM:613235	TAS					C	HPO:skoehler[2010-06-19]
OMIM:613235	Factor XIIIB deficiency		HP:0040234	PMID:11313256	PCS		2/2			P	HPO:probinson[2022-09-25]
OMIM:613235	Factor XIIIB deficiency		HP:0031364	OMIM:613235	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613235	Factor XIIIB deficiency		HP:0000007	PMID:8324218	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-25]
OMIM:613235	Factor XIIIB deficiency		HP:0000978	OMIM:613235	TAS					P	HPO:skoehler[2010-06-19]
OMIM:613235	Factor XIIIB deficiency		HP:0008357	PMID:8324218;PMID:11313256	PCS		3/3			P	HPO:probinson[2022-09-25];HPO:probinson[2013-12-15];HPO:probinson[2022-09-25]
OMIM:613235	Factor XIIIB deficiency		HP:0004846	PMID:11313256	PCS		1/2			P	HPO:probinson[2013-12-15];HPO:probinson[2022-09-25]
OMIM:613235	Factor XIIIB deficiency		HP:0011884	PMID:11313256	PCS	HP:0003623	1/2			P	HPO:probinson[2013-12-15];HPO:probinson[2022-09-25]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0004432	OMIM:200900	TAS					P	HPO:probinson[2009-02-17]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0003819	OMIM:200900	TAS					C	HPO:probinson[2009-02-17]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0005871	OMIM:200900	TAS					P	HPO:probinson[2009-02-17]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0004430	OMIM:200900	TAS					P	HPO:skoehler[2015-01-21]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0000778	OMIM:200900	TAS					P	HPO:probinson[2009-02-17]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0000007	OMIM:200900	TAS					I	HPO:probinson[2009-02-17]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0001888	OMIM:200900	TAS					P	HPO:probinson[2009-02-17]
OMIM:200900	Achondroplasia, so-called, and severe combined immunodeficiency		HP:0000765	OMIM:200900	IEA					P	HPO:probinson[2009-02-17]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0004313	PMID:25843314;PMID:22197273	PCS		6/19			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0005523	PMID:25843314;PMID:22801960	PCS		9/25			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0033509	PMID:25843314	PCS		1/7			P	HPO:probinson[2021-02-13]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0001541	OMIM:615122	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0020072	PMID:25843314;PMID:22197273	PCS		15/29			P	HPO:skoehler[2019-02-22];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0000155	PMID:25843314	PCS		4/17		HP:0033185	P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0033508	PMID:25843314	PCS		1/17			P	HPO:probinson[2021-02-13]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0002240	PMID:22197273	PCS		2/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0032170	PMID:25843314	PCS		1/17			P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0012156	PMID:25843314;PMID:22801960	PCS		5/25		HP:0033185	P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0012189	PMID:25843314	PCS		3/17			P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0031381	PMID:22197273	PCS					P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0001915	PMID:25843314;PMID:22197273	PCS		2/19			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0002719	PMID:25843314	PCS					P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0100806	PMID:25843314	PCS		1/17			P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0002716	PMID:25843314;PMID:22197273	PCS		10/19		HP:0033185;HP:0033185	P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0000007	PMID:22197273	PCS					I	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0001945	PMID:25843314;PMID:22197273	PCS		6/19		HP:0033185	P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0006532	PMID:25843314	PCS		3/17			P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0000554	PMID:25843314	PCS		4/17		HP:0033185	P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0001433	PMID:25843314	PCS		5/17		HP:0033185	P	HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0001744	PMID:22197273	PCS		2/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0001876	PMID:25843314	PCS		1/17			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06]
OMIM:615122	Lymphoproliferative syndrome 2		HP:0002665	PMID:22801960	PCS		2/8			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-06]
OMIM:618406	Body mass index quantitative trait locus 20		HP:0000098	PMID:12646665	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-15]
OMIM:618406	Body mass index quantitative trait locus 20		HP:0011001	PMID:12646665	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-15]
OMIM:618406	Body mass index quantitative trait locus 20		HP:0002591	PMID:12646665	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-15]
OMIM:618406	Body mass index quantitative trait locus 20		HP:0000007	PMID:12646665	PCS					I	HPO:probinson[2019-09-15]
OMIM:618406	Body mass index quantitative trait locus 20		HP:0001513	PMID:12646665	PCS					P	HPO:probinson[2019-09-15]
OMIM:618406	Body mass index quantitative trait locus 20		HP:0000842	PMID:12646665	PCS					P	HPO:probinson[2019-09-15]
OMIM:618406	Body mass index quantitative trait locus 20		HP:0000006	PMID:12646665	PCS					I	HPO:probinson[2019-09-15]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0002223	PMID:34999892	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0034572	PMID:34999892	PCS		1/2			P	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0011463	PMID:34999892	PCS		3/4			C	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0200016	PMID:34999892	PCS		4/4			P	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0003593	PMID:34999892	PCS		1/4			C	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0001070	PMID:34999892	PCS		4/4			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0002209	PMID:34999892	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0000007	PMID:34999892	PCS					I	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0000653	PMID:34999892	PCS		4/4			P	HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0045075	PMID:34999892	PCS		1/4			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620199	Inflammatory poikiloderma with hair abnormalities and acral keratoses		HP:0001029	PMID:34999892	PCS		4/4			P	HPO:probinson[2023-06-11]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0001770	PMID:2319886;PMID:10069712	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0003189	PMID:10069712	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0000540	OMIM:184460	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0000430	PMID:10069712	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0000381	OMIM:184460	TAS	HP:0003577	HP:0040281			P	HPO:probinson[2012-07-31]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0011304	OMIM:184460	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0009177	OMIM:184460	TAS					P	HPO:skoehler[2012-10-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0010055	OMIM:184460	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0002949	PMID:2319886	PCS		2/5			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0009882	PMID:2319886	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0000405	OMIM:184460	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0009765	PMID:2319886	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0000466	PMID:2319886;PMID:10069712	PCS		3/6			P	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0000006	OMIM:184460;PMID:2319886;PMID:10069712	PCS					I	HPO:iea[2009-02-17]
OMIM:184460	Stapes ankylosis with broad thumb and toes		HP:0007943	OMIM:184460	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0005227	PMID:21416598;PMID:15042511	PCS		5/17			P	HPO:probinson[2013-03-05];HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0002223	PMID:21416598	PCS		3/5			P	HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0003002	PMID:21416598	PCS	HP:0003596	1/5			P	HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0003003	PMID:21416598	PCS	HP:0003596	1/5			P	HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0002231	PMID:21416598	PCS		1/5			P	HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0002209	PMID:21416598	PCS		3/5			P	HPO:skoehler[2013-07-30];HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0010764	PMID:21416598	PCS		1/5			P	HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0000006	PMID:15042511	PCS					I	HPO:probinson[2013-01-09]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0000677	PMID:21416598;PMID:15042511	PCS		15/15			P	HPO:probinson[2013-03-05];HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0033769	PMID:21416598	PCS		1/5			P	HPO:probinson[2021-07-10]
OMIM:608615	Oligodontia-colorectal cancer syndrome		HP:0002215	PMID:21416598	PCS		1/5			P	HPO:probinson[2021-07-10]
OMIM:300914	Deafness, X-linked 6		HP:0003577	PMID:23714752	PCS		4/4	MALE		C	HPO:probinson[2022-08-07]
OMIM:300914	Deafness, X-linked 6		HP:0008619	PMID:23714752	PCS	HP:0003577	4/4	MALE		P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:300914	Deafness, X-linked 6		HP:0001419	PMID:23714752	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2022-08-07]
OMIM:300914	Deafness, X-linked 6		HP:0011373	PMID:23714752	PCS		4/4	MALE		P	HPO:probinson[2022-08-07]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000044	PMID:32620954	PCS					P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000054	PMID:32620954	PCS		11/12			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0003577	PMID:32620954	PCS					C	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0002650	PMID:32620954	PCS		1/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0001382	PMID:32620954	PCS		4/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000691	PMID:32620954	PCS		1/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0010522	PMID:32620954	PCS		1/12			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0011069	PMID:32620954	PCS		1/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0011318	PMID:32620954	PCS		1/14			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0011326	PMID:32620954	PCS		1/14			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000939	PMID:32620954	PCS		2/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0002808	PMID:32620954	PCS		1/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000729	PMID:32620954	PCS		3/12			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000938	PMID:32620954	PCS		1/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0011054	PMID:32620954	PCS		1/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000739	PMID:32620954	PCS		1/12			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000458	PMID:32620954	PCS		12/12			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000823	PMID:32620954	PCS					P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000047	PMID:32620954	PCS		2/12			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000006	PMID:32620954	PCS					I	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000028	PMID:32620954	PCS		11/12			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0000699	PMID:32620954	PCS		3/13			P	HPO:probinson[2022-03-20]
OMIM:619718	Hypogonadotropic hypogonadism 26 with or without anosmia		HP:0001249	PMID:32620954	PCS		1/12			P	HPO:probinson[2022-03-20]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0000750	PMID:30970188	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0002373	PMID:30970188	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0001272	PMID:30970188	PCS	HP:0003621	1/3			P	HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0011463	PMID:30970188	PCS		3/3			C	HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0001263	PMID:30970188	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0000007	PMID:30970188	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0002194	PMID:30970188	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0002073	PMID:30970188	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-25]
OMIM:618412	Global developmental delay, progressive ataxia, and elevated glutamine		HP:0003217	PMID:30970188	PCS		3/3			P	HPO:probinson[2023-01-25]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0001265	OMIM:617721	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0003621	PMID:28369220	PCS		7/7			C	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0001288	OMIM:617721	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0001761	OMIM:617721	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0008959	PMID:28369220	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0009053	PMID:28369220	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0007002	PMID:28369220	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0007149	PMID:28369220	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0003438	PMID:28369220	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0000006	PMID:28369220	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0003677	PMID:28369220	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0008944	PMID:28369220	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617721	Neuronopathy, distal hereditary motor, type IX		HP:0006844	PMID:28369220	PCS		4/7			P	HPO:probinson[2023-02-11]
OMIM:140350	Hawkinsinuria		HP:0000252	PMID:11073718	PCS		1/3			P	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0003231	PMID:11073718	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:6001004	OMIM:140350	TAS					P	HPO:probinson[2024-08-03]
OMIM:140350	Hawkinsinuria		HP:0003593	PMID:11073718	PCS		3/3			C	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0003161	PMID:11073718	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0034457	PMID:11073718	PCS		2/2			P	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0008070	PMID:11073718	PCS		1/3			P	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0001508	PMID:11073718	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0000711	PMID:11073718	PCS		1/3			P	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0003607	PMID:11073718	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0001942	OMIM:140350	IEA		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:140350	Hawkinsinuria		HP:0000006	PMID:11073718	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:189150	Toe, rotated fifth		HP:0001597	OMIM:189150	IEA					P	HPO:iea[2009-02-17]
OMIM:189150	Toe, rotated fifth		HP:0000006	OMIM:189150	IEA					I	HPO:iea[2009-02-17]
OMIM:112370	Brachmann-De lange-like facial changes with microcephaly, metatarsusadductus, and developmental delay		HP:0000252	OMIM:112370	IEA					P	HPO:iea[2009-02-17]
OMIM:112370	Brachmann-De lange-like facial changes with microcephaly, metatarsusadductus, and developmental delay		HP:0000271	OMIM:112370	IEA					P	HPO:iea[2009-02-17]
OMIM:112370	Brachmann-De lange-like facial changes with microcephaly, metatarsusadductus, and developmental delay		HP:0007560	OMIM:112370	IEA					P	HPO:iea[2009-02-17]
OMIM:112370	Brachmann-De lange-like facial changes with microcephaly, metatarsusadductus, and developmental delay		HP:0001263	OMIM:112370	IEA					P	HPO:iea[2009-02-17]
OMIM:112370	Brachmann-De lange-like facial changes with microcephaly, metatarsusadductus, and developmental delay		HP:0001510	OMIM:112370	IEA					P	HPO:iea[2009-02-17]
OMIM:112370	Brachmann-De lange-like facial changes with microcephaly, metatarsusadductus, and developmental delay		HP:0001840	OMIM:112370	IEA					P	HPO:iea[2009-02-17]
OMIM:112370	Brachmann-De lange-like facial changes with microcephaly, metatarsusadductus, and developmental delay		HP:0000006	OMIM:112370	IEA					I	HPO:iea[2009-02-17]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0001265	PMID:21820100	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0001883	PMID:21820100	PCS	HP:0003577	1/12			P	HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0000750	PMID:21820100	PCS		2/12			P	HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0001761	PMID:21820100	PCS		10/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0001263	PMID:21820100	PCS		1/12			P	HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0002460	PMID:21820100	PCS		12/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0003690	PMID:21820100	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0001270	PMID:21820100	PCS		8/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0009046	PMID:21820100	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0009830	PMID:21820100	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0002936	PMID:21820100	PCS		6/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0002359	PMID:21820100	PCS		3/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0000006	PMID:21820100	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:614228	Charcot-marie-tooth disease, axonal, type 2O		HP:0003677	PMID:21820100	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:144650	Hyperlipoproteinemia, type V		HP:0000819	OMIM:144650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:144650	Hyperlipoproteinemia, type V		HP:0003233	OMIM:144650	TAS					P	HPO:probinson[2013-03-12]
OMIM:144650	Hyperlipoproteinemia, type V		HP:0003563	OMIM:144650	TAS					P	HPO:probinson[2013-03-31]
OMIM:144650	Hyperlipoproteinemia, type V		HP:0003362	OMIM:144650	TAS					P	HPO:probinson[2013-03-12]
OMIM:144650	Hyperlipoproteinemia, type V		HP:0000006	OMIM:144650	TAS					I	HPO:probinson[2009-02-17]
OMIM:144650	Hyperlipoproteinemia, type V		HP:0012238	OMIM:144650	TAS					P	HPO:probinson[2013-04-01]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0000132	PMID:24958846	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0011463	PMID:24958846	PCS		3/3			C	HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0003010	PMID:24958846	PCS		3/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0006298	PMID:24958846	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0000007	PMID:24958846	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0000978	PMID:24958846	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0008148	PMID:24958846	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0000421	PMID:24958846	PCS		3/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-22]
OMIM:615888	Bleeding disorder, platelet-type, 18		HP:0004866	PMID:24958846	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0008936	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0002487	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0000483	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0002059	PMID:30323019	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0002015	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0002521	PMID:30323019	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0002540	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0002188	PMID:30323019	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0031936	PMID:30323019	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0002079	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0001263	PMID:30323019	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0003593	PMID:30323019	PCS		2/2			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0030891	PMID:30323019	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0012469	PMID:30323019	PCS		2/2			P	HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0100704	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0000817	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0200134	PMID:30323019	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0025336	PMID:30323019	PCS		2/2			P	HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0000565	PMID:30323019	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618374	Epileptic encephalopathy, early infantile, 72		HP:0000006	PMID:30323019	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0004754	PMID:25351925	PCS		2/21			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0001297	PMID:25351925	PCS		2/8			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0003621	PMID:25351925	PCS		2/7			C	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0003596	PMID:25351925	PCS		11/28			C	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0003584	PMID:25351925	PCS		2/21			C	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0005110	PMID:25351925	PCS		4/8			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0011711	PMID:25351925	PCS		1/21			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0030718	PMID:25351925	PCS		2/8			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0011713	PMID:25351925	PCS		1/8			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0005184	PMID:25351925	PCS		2/8			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0031295	PMID:25351925;OMIM:617047	PCS		3/18			P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04];HPO:skoehler[2018-10-08]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0001639	PMID:25351925	PCS					P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0011463	PMID:25351925	PCS		1/7			C	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0011462	PMID:25351925	PCS		12/28			C	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0001635	PMID:25351925	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0001653	OMIM:617047	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0000006	PMID:25351925	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0001645	PMID:25351925	PCS		5/21			P	HPO:probinson[2022-07-04]
OMIM:617047	Cardiomyopathy, familial hypertrophic, 26		HP:0001678	PMID:25351925	PCS		1/8			P	HPO:probinson[2022-07-04]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002067	PMID:11007980	PCS		4/4	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001332	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001250	PMID:12615169	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001371	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002186	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002064	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0003593	PMID:10986043	PCS		2/2			C	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001251	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0010845	PMID:10986043	PCS		1/2			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000712	PMID:12325019	PCS		1/5	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000711	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0025336	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001249	PMID:11309367	PCS		20/20			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001249	PMID:10986043	PCS		2/2			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001249	PMID:12325019	PCS		5/5	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002751	PMID:11309367	PCS		3/20			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000297	PMID:10986043	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0003763	PMID:10986043	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002510	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000252	PMID:11007980	PCS		2/2	FEMALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000252	PMID:11007980	PCS		0/4	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000252	PMID:12615169	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001300	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001344	PMID:12615169;PMID:10986043	PCS		3/3			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000771	PMID:12325019	PCS		1/5	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001266	PMID:10986043	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0003487	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000053	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001263	PMID:12615169;PMID:10986043	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001419	PMID:10986043	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000729	PMID:12325019	PCS		1/5	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002307	PMID:10986043	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001258	PMID:10986043	PCS		2/2			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000400	PMID:11309367	PCS		3/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001337	PMID:11309367	PCS		3/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001337	PMID:12325019	PCS		1/5	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0003677	OMIM:300055	IEA					C	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002104	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002322	PMID:11007980	PCS		4/4	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002362	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000218	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001347	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0008936	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0002650	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000750	PMID:11309367	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000750	PMID:11007980	PCS		4/4	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001761	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0031936	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0003781	OMIM:300055	TAS					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000470	OMIM:300055	IEA					P	HPO:iea[2009-02-17]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0032988	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000709	PMID:11309367	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001239	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001118	PMID:10986043	PCS		1/2			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0200055	PMID:12615169	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000026	PMID:12325019	PCS		1/5	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001513	PMID:11309367	PCS		3/20			P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0001513	PMID:12325019	PCS		1/5	MALE		P	HPO:probinson[2021-09-28]
OMIM:300055	Intellectual developmental disorder, X-linked syndromic 13		HP:0000347	OMIM:300055	TAS					P	HPO:iea[2009-02-17]
OMIM:182950	Spinal arachnoiditis		HP:0000924	OMIM:182950	IEA					P	HPO:iea[2009-02-17]
OMIM:182950	Spinal arachnoiditis		HP:0001939	OMIM:182950	IEA					P	HPO:iea[2009-02-17]
OMIM:182950	Spinal arachnoiditis		HP:0000006	OMIM:182950	IEA					I	HPO:iea[2009-02-17]
OMIM:182950	Spinal arachnoiditis		HP:0002313	OMIM:182950	IEA					P	HPO:iea[2009-02-17]
OMIM:619081	Deafness, autosomal dominant 78		HP:0003577	PMID:32294086	PCS		8/8			C	HPO:probinson[2024-03-16]
OMIM:619081	Deafness, autosomal dominant 78		HP:0100753	PMID:32294086	PCS		0/8			P	HPO:probinson[2020-12-10];HPO:probinson[2024-03-16]
OMIM:619081	Deafness, autosomal dominant 78		HP:0001263	PMID:32294086	IEA		0/8			P	HPO:probinson[2020-12-10];HPO:probinson[2024-03-16]
OMIM:619081	Deafness, autosomal dominant 78		HP:0001270	PMID:32294086	PCS	HP:0003593	2/8			P	HPO:probinson[2020-12-10]
OMIM:619081	Deafness, autosomal dominant 78		HP:0011476	PMID:32294086	PCS	HP:0003577	8/8			P	HPO:probinson[2020-12-10]
OMIM:619081	Deafness, autosomal dominant 78		HP:0000256	PMID:32294086	PCS		0/8			P	HPO:probinson[2020-12-10];HPO:probinson[2024-03-16]
OMIM:619081	Deafness, autosomal dominant 78		HP:0000006	PMID:32294086	PCS					I	HPO:probinson[2020-12-10];HPO:probinson[2020-12-10]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0002014	PMID:23114594	PCS	HP:0003623	2/2			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0002243	PMID:23114594	PCS		2/2			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0002013	PMID:23114594	PCS					P	HPO:skoehler[2014-07-11];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0003124	PMID:23114594	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0003077	PMID:23114594	PCS		2/2			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0001508	PMID:23114594	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0011848	PMID:23114594	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0011473	PMID:23114594	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0003073	PMID:23114594	PCS					P	HPO:skoehler[2014-07-11];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0000007	PMID:23114594	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:615863	Diarrhea 7, protein-losing Enteropathy type		HP:0003623	PMID:23114594	PCS		2/2			C	HPO:probinson[2022-09-06]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0001650	PMID:23031282	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-30]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0003577	PMID:23031282	PCS		10/10			C	HPO:probinson[2022-05-30]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0001629	PMID:23031282	PCS		6/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-30]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0001719	PMID:23031282	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-30]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0005110	OMIM:617912	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0003829	OMIM:617912	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0001647	OMIM:617912	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0001636	PMID:23031282	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-30]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0000007	OMIM:617912	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0001631	PMID:23031282	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-30]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0000006	PMID:23031282	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-30]
OMIM:617912	Congenital heart defects, multiple types, 5		HP:0001644	OMIM:617912	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002168	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0003577	PMID:33639315	PCS		1/1			C	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0003236	PMID:29855340;PMID:33639315	PCS		3/3			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002121	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001252	PMID:29855340;PMID:33639315	PCS		3/3			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001251	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0003593	PMID:29855340	PCS		2/2			C	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0032794	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0012389	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0100651	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0011182	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0000639	PMID:29855340;PMID:33639315	PCS		3/3			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0011463	PMID:34167170	PCS		1/2			C	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002878	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002119	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0025116	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002359	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001324	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0003701	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001268	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0008936	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002058	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0003323	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002015	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0011968	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002197	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002098	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001260	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0030046	PMID:29855340	PCS		1/1			P	HPO:probinson[2023-04-20];HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001284	PMID:34167170;PMID:29855340	PCS		2/4			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0012736	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0000007	PMID:29855340	PCS					I	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001558	PMID:33639315	PCS		1/1			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002505	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0007359	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0001730	PMID:34167170	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:620166	Muscular dystrophy, congenital, with or without seizures		HP:0002027	PMID:29855340	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0006824	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0002650	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0002023	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0000519	PMID:5694533	PCS					P	HPO:lccarmody[2009-02-17]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0002814	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0000007	PMID:5694533	PCS					I	HPO:lccarmody[2009-02-17]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0009136	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0000505	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0001093	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0002655	PMID:5694533	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:246000	Leg, absence deformity of, with congenital cataract		HP:0007834	PMID:5694533	PCS	HP:0003577				P	HPO:lccarmody[2018-06-27]
OMIM:278850	46,XX sex reversal 2		HP:0000054	OMIM:278850	TAS					P	HPO:skoehler[2015-07-26]
OMIM:278850	46,XX sex reversal 2		HP:0008726	OMIM:278850	TAS					P	HPO:skoehler[2015-07-26]
OMIM:278850	46,XX sex reversal 2		HP:0000046	OMIM:278850	TAS					P	HPO:skoehler[2015-07-26]
OMIM:278850	46,XX sex reversal 2		HP:0000013	OMIM:278850	TAS					P	HPO:skoehler[2015-07-26]
OMIM:278850	46,XX sex reversal 2		HP:0000051	OMIM:278850	TAS					P	HPO:skoehler[2015-07-26]
OMIM:278850	46,XX sex reversal 2		HP:0011969	PMID:21653197	PCS		2/2			P	HPO:probinson[2024-03-09]
OMIM:278850	46,XX sex reversal 2		HP:0040171	PMID:21653197	PCS		2/2			P	HPO:skoehler[2015-08-05];HPO:probinson[2024-03-09]
OMIM:278850	46,XX sex reversal 2		HP:0010459	OMIM:278850	TAS					P	HPO:iea[2013-02-23]
OMIM:278850	46,XX sex reversal 2		HP:0011961	PMID:21653197	PCS		2/2			P	HPO:probinson[2024-03-09]
OMIM:278850	46,XX sex reversal 2		HP:0011842	PMID:21653197	PCS		0/2			P	HPO:probinson[2024-03-09]
OMIM:278850	46,XX sex reversal 2		HP:0012861	OMIM:278850	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:278850	46,XX sex reversal 2		HP:0012245	PMID:21208124	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-07]
OMIM:278850	46,XX sex reversal 2		HP:0011462	PMID:21653197	PCS		2/2			C	HPO:probinson[2024-03-09]
OMIM:278850	46,XX sex reversal 2		HP:0008232	PMID:21653197	PCS		2/2			P	HPO:probinson[2024-03-09]
OMIM:278850	46,XX sex reversal 2		HP:0000789	PMID:21653197;PMID:21208124	PCS		5/5			P	HPO:probinson[2024-03-09]
OMIM:278850	46,XX sex reversal 2		HP:0000048	OMIM:278850	TAS					P	HPO:skoehler[2015-07-26]
OMIM:278850	46,XX sex reversal 2		HP:0000006	PMID:21208124	PCS					I	HPO:iea[2013-02-23];HPO:probinson[2023-04-07]
OMIM:278850	46,XX sex reversal 2		HP:0000027	PMID:21208124	PCS		3/3			P	HPO:iea[2013-02-23];HPO:probinson[2024-03-09]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0011939	PMID:24906020	PCS		1/6			P	HPO:probinson[2024-07-22]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000286	PMID:24906020	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0003577	PMID:24906020	PCS		6/6			C	HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000343	PMID:24906020	PCS		1/6			P	HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0008905	PMID:24906020	PCS		2/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000486	PMID:24906020	PCS		2/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0009918	OMIM:615877	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000482	PMID:24906020	PCS		2/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000518	OMIM:615877	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000639	OMIM:615877	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0011220	OMIM:615877	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0001126	PMID:24906020	PCS		1/5			P	HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000256	PMID:24906020	PCS		2/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0001763	PMID:24906020	PCS		1/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0005001	PMID:24906020	PCS		1/6			P	HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0004691	PMID:24906020	PCS		1/6			P	HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000826	PMID:24906020	PCS		1/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000528	PMID:24906020	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000629	OMIM:615877	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000007	OMIM:615877	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000568	PMID:24906020	PCS		2/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000527	OMIM:615877	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000647	PMID:24906020	PCS		1/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000047	PMID:24906020	PCS		1/5	MALE		P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000006	PMID:24906020	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:615877	Microphthalmia/coloboma and skeletal dysplasia syndrome		HP:0000589	PMID:24906020	PCS		4/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-06]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0003577	PMID:15756637	PCS		12/12			C	HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0000232	OMIM:242500	IEA					P	HPO:iea[2009-02-17]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0002063	OMIM:242500	TAS					P	HPO:iea[2009-02-17]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0001270	PMID:15756637	PCS		1/12			P	HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0009381	OMIM:242500	IEA					P	HPO:iea[2009-02-17]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0001508	PMID:15756637	PCS		3/12			P	HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0007431	PMID:15756637	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0000007	PMID:15756637	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0000656	PMID:15756637	PCS		3/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0003811	PMID:15756637	PCS		2/12			C	HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0001522	PMID:15756637	PCS		2/12			C	HPO:probinson[2023-02-26]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0000520	OMIM:242500	TAS					P	HPO:iea[2009-02-17]
OMIM:242500	Ichthyosis, congenital, autosomal recessive 4B		HP:0001622	PMID:15756637	PCS		9/12			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:619095	Spermatogenic failure 46		HP:0033393	PMID:32619401;PMID:32681648	PCS		4/4			P	HPO:probinson[2021-02-13]
OMIM:619095	Spermatogenic failure 46		HP:0032560	PMID:32619401;PMID:32681648	PCS		4/4			P	HPO:probinson[2020-12-12]
OMIM:619095	Spermatogenic failure 46		HP:0003251	PMID:32619401;PMID:32681648	PCS		4/4			P	HPO:probinson[2020-12-12]
OMIM:619095	Spermatogenic failure 46		HP:0003581	PMID:32619401	PCS		3/3			C	HPO:probinson[2020-12-12]
OMIM:619095	Spermatogenic failure 46		HP:0000007	PMID:32619401	PCS					I	HPO:probinson[2020-12-12];HPO:probinson[2020-12-12]
OMIM:619095	Spermatogenic failure 46		HP:0012207	PMID:32619401;PMID:32681648	PCS		4/4			P	HPO:probinson[2020-12-12]
OMIM:619095	Spermatogenic failure 46		HP:0032558	PMID:32681648	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619095	Spermatogenic failure 46		HP:0032559	PMID:32619401;PMID:32681648	PCS		4/4			P	HPO:probinson[2020-12-12]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003676	OMIM:609286	IEA					C	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0008209	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001250	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003690	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0011675	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003390	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000819	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000716	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000518	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003701	OMIM:609286	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003548	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000135	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003688	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003546	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003689	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003326	OMIM:609286	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003323	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001265	OMIM:609286	TAS					P	HPO:skoehler[2012-11-21]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0002059	OMIM:609286	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0002015	OMIM:609286	TAS	HP:0003584				P	HPO:skoehler[2012-11-21]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001300	OMIM:609286	TAS		HP:0040284			P	HPO:skoehler[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003200	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001662	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001288	OMIM:609286	TAS	HP:0003584				P	HPO:skoehler[2012-11-21]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000590	OMIM:609286	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:skoehler[2010-06-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001260	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001263	OMIM:609286	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0002151	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003581	OMIM:609286	TAS					C	HPO:skoehler[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001284	OMIM:609286	TAS					P	HPO:skoehler[2012-11-21]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0010871	OMIM:609286	TAS					P	HPO:skoehler[2012-11-21]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0012378	OMIM:609286	TAS					P	HPO:skoehler[2013-10-22]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001618	OMIM:609286	TAS	HP:0003584				P	HPO:skoehler[2012-11-21]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000726	OMIM:609286	TAS	HP:0003584				P	HPO:skoehler[2012-11-21]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000508	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001638	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0001730	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000006	OMIM:609286	IEA					I	HPO:iea[2009-02-17]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0000820	OMIM:609286	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609286	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3		HP:0003458	OMIM:609286	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0001650	PMID:34072542	PCS		1/69			P	HPO:probinson[2021-07-01]
OMIM:230800	Gaucher disease, type I		HP:0001971	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:6001185	PMID:21868580	PCS		64/64			P	HPO:probinson[2025-09-26]
OMIM:230800	Gaucher disease, type I		HP:0002240	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0010885	OMIM:230800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:230800	Gaucher disease, type I		HP:0001903	OMIM:230800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:230800	Gaucher disease, type I		HP:0006530	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0000953	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0007401	OMIM:230800	TAS					P	HPO:skoehler[2015-07-26]
OMIM:230800	Gaucher disease, type I		HP:0006775	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0002953	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0002756	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0001744	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0000478	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0004975	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0002113	OMIM:230800	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0002653	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0002094	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0002092	PMID:34072542	PCS		9/69			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230800	Gaucher disease, type I		HP:0000822	OMIM:230800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230800	Gaucher disease, type I		HP:0000007	PMID:3353383	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230800	Gaucher disease, type I		HP:0000421	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:230800	Gaucher disease, type I		HP:0001873	OMIM:230800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:230800	Gaucher disease, type I		HP:0001653	PMID:34072542	PCS		33/69			P	HPO:probinson[2021-07-01]
OMIM:230800	Gaucher disease, type I		HP:0001876	OMIM:230800	IEA					P	HPO:iea[2009-02-17]
OMIM:247450	Lymphoblastic transformation, intrinsic defect in		HP:0001939	OMIM:247450	IEA					P	HPO:iea[2009-02-17]
OMIM:247450	Lymphoblastic transformation, intrinsic defect in		HP:0002728	OMIM:247450	IEA					P	HPO:iea[2009-02-17]
OMIM:247450	Lymphoblastic transformation, intrinsic defect in		HP:0000007	OMIM:247450	IEA					I	HPO:iea[2009-02-17]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001276	PMID:27453578	PCS		5/7			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0003577	PMID:27453578	PCS		7/7			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000340	PMID:27453578	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0002365	PMID:27453578	PCS		0/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0004322	OMIM:617090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001250	PMID:27453578	PCS		0/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001274	OMIM:617090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0010862	PMID:27453578	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001508	OMIM:617090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0045028	OMIM:617090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0012471	PMID:27453578	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000316	OMIM:617090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000414	OMIM:617090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0002119	OMIM:617090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001249	PMID:27453578	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001347	PMID:27453578	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000750	PMID:27453578	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001321	PMID:27453578	PCS		0/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0002079	PMID:27453578	PCS		4/5			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001263	PMID:27453578	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000294	PMID:27453578	PCS		1/7			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0002194	PMID:27453578	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0012434	PMID:27453578	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0011451	PMID:27453578	PCS		7/7			P	HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000007	PMID:27453578	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000400	PMID:27453578	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0001257	PMID:27453578	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0000104	OMIM:617090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617090	Microcephaly 17, primary, autosomal recessive		HP:0009879	PMID:27453578	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0000044	PMID:29749493;PMID:24355708	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0002168	OMIM:215470	IEA					P	HPO:iea[2009-02-17]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0003676	PMID:24355708	PCS					C	HPO:skoehler[2014-03-24];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0010627	PMID:29749493;PMID:24355708	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0001135	PMID:24355708	PCS		8/9			P	HPO:skoehler[2009-02-17];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0001272	PMID:29749493;PMID:24355708	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:skoehler[2010-06-18];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0003693	PMID:24355708	PCS		5/9			P	HPO:skoehler[2014-03-24];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0002066	PMID:29749493;PMID:24355708	PCS		9/10			P	ORCID:0000-0002-0736-9199[2024-05-19];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0001251	OMIM:215470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0002061	PMID:24355708	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0033206	PMID:24355708	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0002080	OMIM:215470	IEA					P	HPO:iea[2009-02-17]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0030339	PMID:25299038	PCS					P	HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0007083	PMID:24355708	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0011463	PMID:24355708	PCS		4/9			C	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0007263	OMIM:215470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0000613	OMIM:215470	IEA					P	HPO:iea[2009-02-17]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0007722	PMID:29749493	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0000556	OMIM:215470	IEA					P	HPO:iea[2009-02-17]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0000533	PMID:24355708	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0001265	PMID:29749493;PMID:24355708	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:skoehler[2014-03-24];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0011808	PMID:24355708	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0003621	PMID:29749493;PMID:24355708	PCS		6/10			C	HPO:skoehler[2009-02-17];HPO:probinson[2024-05-19];ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0003487	PMID:24355708	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0030344	PMID:29749493	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0001284	OMIM:215470	TAS					P	HPO:skoehler[2014-03-24]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0030341	PMID:29749493	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0002075	PMID:29749493	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0040171	PMID:29749493	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0009072	PMID:24355708	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0000529	PMID:24355708	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0000007	PMID:24355708	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0001257	PMID:24355708	PCS		3/9			P	HPO:skoehler[2014-03-24];HP:probinson[2019-03-09]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0002127	OMIM:215470	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:215470	Boucher-Neuhauser syndrome		HP:0000786	PMID:24355708	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0002960	OMIM:243150	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0025023	PMID:15137007	PCS		9/13			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0003577	PMID:23830146	PCS		5/5			C	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0005214	PMID:23423984	PCS	HP:0011461	3/3			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001894	PMID:29174094	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0005235	PMID:15137007	PCS		15/16			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0004387	PMID:23830146	PCS		5/5			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001890	OMIM:243150	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0025085	PMID:29174094	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0010448	PMID:15137007	PCS		13/15			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001629	PMID:15137007	PCS		1/16			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0011100	PMID:23830146;PMID:23423984;PMID:15137007	PCS		20/27			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0032220	PMID:29174094	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0011220	PMID:29174094	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0006297	PMID:29174094	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0000316	PMID:29174094	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0000778	OMIM:243150	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0012190	PMID:23830146	PCS		8/8			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001888	PMID:23830146	PCS		3/5			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001522	PMID:23830146	PCS		3/5			C	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0003347	PMID:23830146	PCS		4/8			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0003765	OMIM:243150	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0010959	PMID:15137007	PCS		1/16			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0004313	PMID:29174094;PMID:23830146	PCS		7/14			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001561	PMID:23423984	PCS	HP:0011461	1/3			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0002573	PMID:23830146	PCS		3/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0004432	PMID:23830146	PCS		2/8			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0004430	OMIM:243150	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0011102	PMID:29174094	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0003819	PMID:23830146	PCS		1/5			C	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0000007	PMID:23423984	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001539	PMID:23423984;PMID:15137007	PCS		2/19			P	HPO:probinson[2022-03-19];HPO:skoehler[2013-05-31];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001511	PMID:15137007	PCS		5/16			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0002205	PMID:29174094	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0002247	PMID:15137007	PCS		9/16			P	HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0002566	PMID:15137007	PCS		3/16			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-03-19]
OMIM:243150	Gastrointestinal defects and immunodeficiency syndrome		HP:0001974	PMID:29174094	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:610099	Myopathy, distal 3		HP:0001760	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0002312	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0003376	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0003693	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0003694	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0002460	OMIM:610099	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0003560	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0001171	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0008180	OMIM:610099	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610099	Myopathy, distal 3		HP:0009473	OMIM:610099	TAS		20/20		HP:0012825	P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0003805	OMIM:610099	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610099	Myopathy, distal 3		HP:0000006	OMIM:610099	IEA					I	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0003677	OMIM:610099	IEA					C	HPO:iea[2009-02-17]
OMIM:610099	Myopathy, distal 3		HP:0003458	OMIM:610099	IEA					P	HPO:iea[2009-02-17]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0003621	PMID:35013551	PCS		5/5			C	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0001310	PMID:35013551	PCS		1/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0000023	PMID:35013551	PCS		2/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0002075	PMID:35013551	PCS		1/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0003393	PMID:35013551	PCS		4/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0033685	PMID:35013551	PCS		1/2			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0007181	PMID:35013551	PCS		4/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0009053	PMID:35013551	PCS		3/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0000007	PMID:35013551	PCS					I	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0002216	PMID:35013551	PCS		1/5			P	HPO:probinson[2022-08-10];HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0002522	PMID:35013551	PCS		2/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0001249	PMID:35013551	PCS		0/5			P	HPO:probinson[2022-08-10]
OMIM:619903	Peripheral motor neuropathy, childhood-onset, biotin-responsive		HP:0001644	PMID:35013551	PCS		1/5			P	HPO:probinson[2022-08-10]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0001792	OMIM:119580	TAS					P	HPO:skoehler[2012-10-17]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0002023	PMID:28301459	PCS		2/8			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0000453	PMID:28301459	PCS		1/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0002164	PMID:28301459	PCS		5/8			P	HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0012905	PMID:28301459	PCS		8/8			P	HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0030001	PMID:28301459	PCS		8/8			P	HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0004471	PMID:28301459	PCS		2/8			P	HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0012725	PMID:28301459	PCS		2/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0012368	PMID:28301459	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0008070	PMID:28301459	PCS		7/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0009890	OMIM:119580	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0045005	PMID:28301459	PCS		2/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0007651	PMID:28301459	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0000316	PMID:28301459	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0000668	OMIM:119580	TAS					P	HPO:skoehler[2012-10-17]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0000348	PMID:28301459	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0030084	OMIM:119580	TAS					P	HPO:skoehler[2014-09-21]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0009743	PMID:28301459	PCS		8/8			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0000006	PMID:28301459	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0000204	PMID:28301459	PCS		7/8			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-12]
OMIM:119580	Blepharocheilodontic syndrome 1		HP:0000698	PMID:28301459	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:139650	Hairy palms and soles		HP:0001034	OMIM:139650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:139650	Hairy palms and soles		HP:0000006	OMIM:139650	IEA					I	HPO:iea[2009-02-17]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0001892	OMIM:187800	TAS					P	HPO:probinson[2012-05-30]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0001903	OMIM:187800	IEA					P	HPO:iea[2009-02-17]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0003540	OMIM:187800	TAS					P	HPO:probinson[2013-03-12]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0000967	OMIM:187800	TAS					P	HPO:iea[2009-02-17]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0001902	PMID:18065693	PCS		5/5			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0040185	PMID:18065693	PCS		5/5			P	HPO:skoehler[2015-12-30];HP:probinson[2019-03-02]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0001873	PMID:18065693	PCS		5/5			P	HP:probinson[2019-03-02]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0000006	PMID:18065693	PCS					I	HPO:probinson[2012-05-30];HP:probinson[2019-03-02]
OMIM:187800	Bleeding disorder, platelet-type, 16		HP:0032438	PMID:18065693	PCS		5/5			P	HPO:skoehler[2019-04-18];HP:probinson[2019-04-19]
OMIM:220150	Hypouricemia, renal, 1		HP:0000791	PMID:14655203	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0034368	PMID:14655203	PCS		2/2			P	HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0000093	PMID:14655203	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0100520	PMID:14655203	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:6000746	PMID:14655203;PMID:12024214	PCS		3/3			P	HPO:probinson[2024-06-29]
OMIM:220150	Hypouricemia, renal, 1		HP:0001919	PMID:14655203	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0025709	PMID:14655203	PCS		1/2			C	HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0008682	PMID:14655203	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0033132	PMID:14655203	PCS		2/2			P	HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0000007	PMID:12024214	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0025710	PMID:14655203	PCS		1/2			C	HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0003537	PMID:14655203;PMID:12024214	PCS		3/3			P	HPO:probinson[2022-11-20];HPO:iea[2009-02-17];HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0003149	PMID:12024214	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-20]
OMIM:220150	Hypouricemia, renal, 1		HP:0003259	PMID:14655203	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:601369	Deafness, autosomal dominant 9		HP:0009591	OMIM:601369	TAS					P	HPO:skoehler[2012-10-16]
OMIM:601369	Deafness, autosomal dominant 9		HP:0003676	PMID:9806553	PCS					C	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-08]
OMIM:601369	Deafness, autosomal dominant 9		HP:0002321	OMIM:601369	TAS					P	HPO:skoehler[2012-10-16]
OMIM:601369	Deafness, autosomal dominant 9		HP:0005102	OMIM:601369	TAS					P	HPO:skoehler[2012-10-16]
OMIM:601369	Deafness, autosomal dominant 9		HP:0008596	PMID:9806553	PCS					P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-08]
OMIM:601369	Deafness, autosomal dominant 9		HP:0011462	PMID:9806553	PCS					C	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-08]
OMIM:601369	Deafness, autosomal dominant 9		HP:0000360	OMIM:601369	TAS					P	HPO:skoehler[2012-10-16]
OMIM:601369	Deafness, autosomal dominant 9		HP:0000006	PMID:9806553	PCS					I	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-08]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0002267	OMIM:253800	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0003236	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000541	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000486	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000540	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0002365	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001371	OMIM:253800	TAS				HP:0003676	P	HPO:skoehler[2013-06-06]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001250	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001274	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001252	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0003593	OMIM:253800	TAS					C	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001290	OMIM:253800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0031882	OMIM:253800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0002084	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0007260	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000518	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001669	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000238	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001324	OMIM:253800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001302	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0007348	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001642	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0003306	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001249	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001644	OMIM:253800	TAS					P	HPO:skoehler[2015-12-30]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0003202	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001685	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0002650	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000496	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001321	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001360	OMIM:253800	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001284	OMIM:253800	TAS					P	HPO:skoehler[2013-01-22]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0002350	OMIM:253800	TAS					P	HPO:skoehler[2013-01-22]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0003560	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0002093	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0008981	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001339	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000007	OMIM:253800	IEA					I	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000568	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000648	OMIM:253800	IEA					P	HPO:iea[2009-02-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0007973	OMIM:253800	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0001631	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0000545	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253800	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4		HP:0002126	OMIM:253800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001331	OMIM:609053;PMID:26590883	PCS		11/12			P	ORCID:0000-0002-0736-9199[2024-04-18];HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0004325	PMID:26590883	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000483	PMID:26590883	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0003577	PMID:26590883;PMID:17460694	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000365	PMID:26590883;PMID:17460694	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000089	PMID:26590883	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0004322	PMID:17452773;PMID:26590883;PMID:17460694	PCS		10/10			P	HPO:probinson[2013-03-26];ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001274	PMID:26590883	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000085	PMID:26590883	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0012506	PMID:26590883	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0012210	PMID:17452773	PCS		HP:0040283			P	HPO:probinson[2013-03-26]
OMIM:609053	Fanconi anemia, complementation group I		HP:0010034	PMID:26590883	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-19]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001629	PMID:26590883	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001903	PMID:17460694	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000957	PMID:26590883	PCS		3/3			P	HPO:skoehler[2019-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0030680	PMID:17452773	PCS		HP:0040283			P	HPO:probinson[2013-03-26]
OMIM:609053	Fanconi anemia, complementation group I		HP:0005528	PMID:17452773	PCS	HP:0011463	7/7			P	HPO:probinson[2013-03-26]
OMIM:609053	Fanconi anemia, complementation group I		HP:0005528	PMID:26590883	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001643	PMID:26590883	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000413	PMID:26590883	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000252	PMID:26590883	PCS		3/3			P	HPO:skoehler[2019-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000076	PMID:26590883	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-04-19]
OMIM:609053	Fanconi anemia, complementation group I		HP:0030048	PMID:26590883	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0003221	PMID:17452773;PMID:26590883	PCS		10/10			P	HPO:probinson[2013-03-26];ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001263	PMID:26590883	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000470	PMID:26590883	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0034323	PMID:26590883	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000609	PMID:26590883	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0002949	PMID:26590883	PCS		2/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0002308	PMID:26590883	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-19]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000007	PMID:17452773;PMID:26590883	PCS		20/20			I	HPO:probinson[2013-03-26];ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000821	PMID:26590883	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000568	PMID:26590883	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0009777	PMID:26590883;PMID:17460694	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-18];HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000405	OMIM:609053	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001511	PMID:26590883	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000543	PMID:26590883	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001631	PMID:26590883	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-19]
OMIM:609053	Fanconi anemia, complementation group I		HP:0009778	PMID:26590883;PMID:17460694	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-19];ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001873	PMID:26590883	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0003974	PMID:17460694	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0002247	PMID:26590883	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0002984	OMIM:609053	IEA					P	HPO:skoehler[2019-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000545	PMID:26590883	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-19]
OMIM:609053	Fanconi anemia, complementation group I		HP:0000325	PMID:26590883	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001875	PMID:26590883	PCS		2/3			P	HPO:skoehler[2019-04-18]
OMIM:609053	Fanconi anemia, complementation group I		HP:0001655	PMID:26590883	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:603218	Huntington disease-like 1		HP:0006999	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0002311	OMIM:603218	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603218	Huntington disease-like 1		HP:0001310	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0001260	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0002283	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0002063	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0002072	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0100754	PMID:10581230	PCS					P	HPO:probinson[2022-11-04]
OMIM:603218	Huntington disease-like 1		HP:0000716	PMID:10581230	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:603218	Huntington disease-like 1		HP:0000726	PMID:10581230	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:603218	Huntington disease-like 1		HP:0000718	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0011462	PMID:10581230	PCS		11/11			C	HPO:probinson[2022-11-04]
OMIM:603218	Huntington disease-like 1		HP:0000739	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0000711	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0002317	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0000746	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0000751	OMIM:603218	IEA					P	HPO:iea[2009-02-17]
OMIM:603218	Huntington disease-like 1		HP:0000006	PMID:10581230	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0031846	PMID:18606301	PCS		1/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0002240	PMID:18606301	PCS		4/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0003593	PMID:18606301	PCS		5/8			C	HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0001290	PMID:18606301	PCS		1/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0001270	PMID:18606301	PCS					P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0100671	PMID:18606301	PCS					P	HPO:probinson[2013-04-04]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0000639	PMID:18606301	PCS		4/8			P	HPO:probinson[2013-04-04];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0011002	PMID:18606301	PCS		8/8			P	HPO:probinson[2013-04-04];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0001903	PMID:18606301	PCS					P	HPO:probinson[2013-04-04]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0000238	PMID:18606301	PCS		1/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0006532	PMID:18606301	PCS					P	HPO:probinson[2013-04-04]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0001522	PMID:18606301	PCS		2/8			C	HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0001744	PMID:18606301	PCS		3/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0003623	PMID:18606301	PCS		3/8			C	HPO:probinson[2021-03-12];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0004315	PMID:18606301	PCS		3/4			P	HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0002850	PMID:18606301	PCS		2/4			P	HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0006956	PMID:18606301	PCS		1/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0002199	PMID:18606301	PCS		2/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0007807	PMID:18606301	PCS					P	HPO:probinson[2013-04-04]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0001263	PMID:18606301	PCS					P	HPO:probinson[2013-04-04]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0040194	PMID:18606301	PCS		1/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0000529	PMID:18606301	PCS		8/8			P	HPO:probinson[2013-04-04];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0003819	PMID:18606301	PCS		1/8			C	HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0000007	PMID:18606301	PCS					I	HPO:probinson[2013-01-09]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0006640	PMID:18606301	PCS		1/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0000648	PMID:18606301	PCS					P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0001510	PMID:18606301	PCS		3/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0000520	PMID:18606301	PCS		1/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-03-12]
OMIM:612301	Osteopetrosis, autosomal recessive 7		HP:0002720	PMID:18606301	PCS		2/4			P	HPO:probinson[2021-03-12]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001265	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0002751	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0003621	OMIM:604563;PMID:12554688	PCS		12/14			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0003431	OMIM:604563	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0003376	PMID:12554688	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001762	OMIM:604563	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001288	PMID:12554688	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001761	PMID:12554688	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001178	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0003693	PMID:12554688	PCS		3/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0003383	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001284	PMID:12554688	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0002460	PMID:12554688	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0003481	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001171	OMIM:604563	TAS					P	HPO:skoehler[2015-12-30]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0003380	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0011463	PMID:12554688	PCS		2/4			C	HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0000407	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0009027	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0000007	PMID:12554688	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0002936	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0000501	OMIM:604563	TAS					P	HPO:iea[2009-02-17]
OMIM:604563	Charcot-Marie-Tooth disease, type 4B2		HP:0001765	OMIM:604563	IEA					P	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0002014	OMIM:600705	IEA					P	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0002289	OMIM:600705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600705	Satoyoshi syndrome		HP:0000013	OMIM:600705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600705	Satoyoshi syndrome		HP:0001596	OMIM:600705	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600705	Satoyoshi syndrome		HP:0002024	OMIM:600705	IEA					P	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0004322	OMIM:600705	IEA					P	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0001156	OMIM:600705	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:600705	Satoyoshi syndrome		HP:0003011	OMIM:600705	IEA					P	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0000141	OMIM:600705	IEA					P	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0003394	OMIM:600705	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600705	Satoyoshi syndrome		HP:0010049	OMIM:600705	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600705	Satoyoshi syndrome		HP:0012378	OMIM:600705	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600705	Satoyoshi syndrome		HP:0008180	OMIM:600705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600705	Satoyoshi syndrome		HP:0010743	OMIM:600705	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600705	Satoyoshi syndrome		HP:0009771	OMIM:600705	IEA					P	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0002857	OMIM:600705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600705	Satoyoshi syndrome		HP:0003745	OMIM:600705	IEA					I	HPO:iea[2009-02-17]
OMIM:600705	Satoyoshi syndrome		HP:0003712	OMIM:600705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600705	Satoyoshi syndrome		HP:0001763	OMIM:600705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001374	PMID:26933038	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0003236	PMID:26933038	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000244	PMID:26933038	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0003593	PMID:26933038	PCS		1/2			C	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0011463	PMID:26933038	PCS		1/2			C	HPO:probinson[2022-09-04];HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0012471	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001169	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000278	PMID:26933038	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001249	PMID:26933038	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000358	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0002751	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000494	PMID:26933038	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0031956	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000574	PMID:26933038	PCS		2/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0012385	PMID:26933038	PCS		3/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001419	PMID:26933038	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000448	OMIM:300280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0003712	PMID:26933038	PCS		3/3		HP:0012828	P	HPO:probinson[2022-09-04];HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001653	PMID:26933038	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000369	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0410018	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000445	PMID:26933038	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0031295	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001822	PMID:26933038	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0002515	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000339	PMID:26933038	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001621	PMID:26933038	PCS		3/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0002910	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001821	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000336	PMID:26933038	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0002996	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000475	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0002650	PMID:26933038	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001762	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001640	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001288	OMIM:300280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000232	PMID:26933038	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001761	PMID:26933038	PCS		2/3		HP:0003676	P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0008141	PMID:26933038	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001639	PMID:26933038	PCS					P	HPO:probinson[2022-09-04]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0009473	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0002808	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0032232	PMID:26933038	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0430028	PMID:26933038	PCS		2/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001712	PMID:26933038	PCS		2/3			P	HPO:probinson[2023-04-09]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001836	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001638	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0001714	OMIM:300280	IEA					P	HPO:iea[2009-02-17]
OMIM:300280	Uruguay faciocardiomusculoskeletal syndrome		HP:0000664	PMID:26933038	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:264060	Prepapillary vascular loops		HP:0000007	OMIM:264060	IEA					I	HPO:iea[2009-02-17]
OMIM:264060	Prepapillary vascular loops		HP:0001626	OMIM:264060	IEA					P	HPO:iea[2009-02-17]
OMIM:264060	Prepapillary vascular loops		HP:0000478	OMIM:264060	IEA					P	HPO:iea[2009-02-17]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0000100	OMIM:613779	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0000793	PMID:15781264	PCS		0/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0005421	PMID:15781264	PCS		2/2			P	HPO:probinson[2022-06-08];HPO:probinson[2013-12-15];HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0000083	OMIM:613779	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0011463	PMID:15781264	PCS		1/1			C	HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0011110	PMID:15781264	PCS		1/1			P	HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0002718	PMID:15781264	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0003593	PMID:15781264	PCS		1/1			C	HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0000007	PMID:15781264	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0001954	PMID:15781264	PCS		1/1			P	HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0002725	PMID:15781264	PCS	HP:0011462	1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-08]
OMIM:613779	Complement component 3 deficiency, autosomal recessive		HP:0006532	PMID:15781264	PCS		2/2			P	HPO:probinson[2022-06-08]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0012132	OMIM:133180	IEA					P	HPO:skoehler[2019-09-07]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0001909	OMIM:133180	IEA					P	HPO:skoehler[2010-06-20]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0001903	OMIM:133180	IEA					P	HPO:skoehler[2019-09-07]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0004808	OMIM:133180	IEA					P	HPO:skoehler[2019-02-22]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0003829	OMIM:133180	IEA					I	HPO:skoehler[2019-02-22]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0002240	OMIM:133180	IEA					P	HPO:skoehler[2019-04-18]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0004828	OMIM:133180	TAS		20/20			P	HPO:probinson[2013-04-05];HPO:iea[2009-02-17]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0001873	OMIM:133180	IEA					P	HPO:skoehler[2019-09-07]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0000006	OMIM:133180	IEA					I	HPO:iea[2009-02-17]
OMIM:133180	Erythroleukemia, familial, susceptibility to		HP:0001744	OMIM:133180	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616629	Senior-Loken syndrome 9		HP:0003774	PMID:26487268	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0001396	PMID:26487268	PCS		1/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000486	PMID:26487268	PCS		1/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0001970	PMID:26487268	PCS		8/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0001263	PMID:26487268	PCS		3/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0001395	PMID:26487268	PCS		2/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000090	PMID:26487268	PCS		7/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0010442	PMID:26487268	PCS		2/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000639	PMID:26487268	PCS		2/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000608	PMID:26487268	PCS		1/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000938	PMID:26487268	PCS		1/8			P	HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000007	PMID:26487268	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000510	PMID:26487268	PCS		7/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000135	PMID:26487268	PCS		1/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0008802	PMID:26487268	PCS		2/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0001513	PMID:26487268	PCS		4/8			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0000556	PMID:26487268	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-21]
OMIM:616629	Senior-Loken syndrome 9		HP:0004469	PMID:26487268	PCS		2/8			P	HPO:probinson[2023-02-21]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0000175	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0000252	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0001660	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0004467	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0000122	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0000430	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0001629	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0002086	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0009882	OMIM:601355	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0000007	OMIM:601355	IEA					I	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0000465	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:601355	Microcephaly, congenital heart disease, unilateral renal agenesis,and hyposegmented lungs		HP:0002324	OMIM:601355	IEA					P	HPO:iea[2009-02-17]
OMIM:192000	Uterine anomalies		HP:0000130	OMIM:192000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:192000	Uterine anomalies		HP:0000813	OMIM:192000	TAS					P	HPO:skoehler[2013-04-14]
OMIM:192000	Uterine anomalies		HP:0000006	OMIM:192000	TAS					I	HPO:skoehler[2009-02-17]
OMIM:265430	Pulmonary hypoplasia, primary		HP:0002089	OMIM:265430	TAS				HP:0012832	P	HPO:probinson[2009-02-17]
OMIM:265430	Pulmonary hypoplasia, primary		HP:0000007	OMIM:265430	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:265430	Pulmonary hypoplasia, primary		HP:0003811	OMIM:265430	IEA					C	HPO:iea[2009-02-17]
OMIM:116300	Cataract 30, multiple types		HP:0003577	PMID:26694549;PMID:28450710	PCS		3/3			C	HPO:probinson[2023-02-22];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:116300	Cataract 30, multiple types		HP:0010693	PMID:19126778	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:116300	Cataract 30, multiple types		HP:0001115	PMID:28450710	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:116300	Cataract 30, multiple types		HP:0000006	PMID:19126778	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:116300	Cataract 30, multiple types		HP:0007657	PMID:26694549	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:617537	Rahman syndrome		HP:0001276	PMID:28475857	PCS	HP:0003623	1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000483	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0003577	PMID:28475857	PCS		1/5			C	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000486	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0033725	PMID:28475857	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0012450	PMID:28475857	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000739	PMID:28475857	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0002119	PMID:28475857	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000256	PMID:28475857	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0001249	PMID:28475857	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0003623	PMID:28475857	PCS		4/5			C	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0002751	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0003764	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0001762	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000293	PMID:28475857	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0011968	PMID:28475857	PCS		2/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0001582	PMID:28475857	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0001263	PMID:28475857	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0012385	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0009890	PMID:28475857	PCS		5/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000506	PMID:28475857	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000646	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0001319	PMID:28475857	PCS	HP:0003623	2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0005616	PMID:28475857	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000028	PMID:28475857	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:617537	Rahman syndrome		HP:0000006	PMID:28475857	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0002179	PMID:31303265	PCS	HP:0003593	1/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000297	PMID:31303265	PCS		2/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000286	PMID:31303265	PCS		2/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000750	PMID:31303265	PCS		19/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0002188	PMID:31303265	PCS		2/11			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0002079	PMID:31303265	IEA		2/11			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0001266	PMID:31303265	PCS		1/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0001250	PMID:31303265	PCS		2/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0001263	PMID:31303265	PCS		19/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0001290	PMID:31303265	PCS		10/18			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0002172	PMID:31303265	PCS		2/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000729	PMID:31303265	PCS		7/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0002307	PMID:31303265	PCS		9/14			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000378	PMID:31303265	PCS		7/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000411	PMID:31303265	PCS		7/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0040326	PMID:31303265	PCS		1/11			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0001257	PMID:31303265	PCS		1/19			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000006	PMID:31303265	PCS					I	HPO:probinson[2020-06-25];HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0001249	PMID:31303265	PCS		10/10			P	HPO:probinson[2020-06-25]
OMIM:618604	Snijders Blok-Fisher syndrome		HP:0000028	PMID:31303265	PCS	HP:0003577	3/11	MALE		P	HPO:probinson[2020-06-25];HPO:probinson[2020-06-25]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0003577	PMID:9916847;PMID:21864452	PCS		5/5			C	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0001674	PMID:9916847	PCS		1/3			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0001651	PMID:9916847	PCS		1/3			P	HPO:probinson[2013-06-05];HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0011565	PMID:21864452	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0033379	PMID:21864452	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0005160	PMID:9916847	PCS		1/3			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0031348	PMID:9916847	PCS		1/3			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0010452	PMID:9916847	PCS		1/3			P	HPO:probinson[2013-06-05];HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0001629	PMID:9916847	PCS		1/3			P	HPO:probinson[2013-06-05];HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0034188	PMID:9916847	PCS		2/3			P	HPO:probinson[2022-04-15]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0012020	PMID:9916847	PCS		1/3			P	HPO:probinson[2013-06-05];HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0011671	PMID:9916847;PMID:21864452	PCS		3/5			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0001669	PMID:21864452	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0006695	PMID:21864452	PCS		2/2			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0001748	PMID:9916847	PCS		1/3			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0004935	PMID:21864452	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:613751	Heterotaxy, visceral, 4, autosomal		HP:0000006	PMID:9916847	PCS					I	HPO:probinson[2013-06-05];HPO:probinson[2022-03-04]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0000164	OMIM:613989	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0003596	PMID:16247010	PCS		3/6			C	HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0004322	PMID:16247010	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0002043	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0002164	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001395	PMID:16247010	PCS		2/6			P	HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0010885	PMID:16247010	PCS		1/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0012227	PMID:16247010	PCS		1/6			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0000939	PMID:16247010	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001508	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0011462	PMID:16247010	PCS		2/6			C	HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0005528	OMIM:613989	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0000972	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0002216	PMID:16247010	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0003743	PMID:16247010	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001644	OMIM:613989	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0007427	PMID:16247010	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0003621	PMID:16247010	PCS		1/6			C	HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0000252	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001321	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001882	OMIM:613989	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0002211	PMID:16247010	PCS		2/6			P	HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001263	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001915	PMID:16247010	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0000007	PMID:16247010	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0008404	PMID:16247010	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0002206	PMID:16247010	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001873	PMID:16247010	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0002745	PMID:16247010	PCS					P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0000006	PMID:16247010	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001876	PMID:16247010	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0002028	OMIM:613989	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613989	Dyskeratosis congenita, autosomal dominant 2		HP:0001875	PMID:16247010	PCS		1/6			P	HPO:probinson[2022-08-23]
DECIPHER:4	Angelman syndrome (Type 1)		HP:0000252	DECIPHER:4	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:4	Angelman syndrome (Type 1)		HP:0002353	DECIPHER:4	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:4	Angelman syndrome (Type 1)		HP:0002078	DECIPHER:4	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:4	Angelman syndrome (Type 1)		HP:0001250	DECIPHER:4	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:4	Angelman syndrome (Type 1)		HP:0001249	DECIPHER:4	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0001650	OMIM:614980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0003577	PMID:20493459	PCS		2/2			C	HPO:probinson[2022-12-05];HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0004764	OMIM:614980	TAS					P	HPO:probinson[2017-06-17]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0001682	PMID:20493459	PCS		1/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0005110	PMID:20493459	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0001629	OMIM:614980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0001647	PMID:20493459	PCS		1/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0001636	OMIM:614980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0001635	PMID:20493459	PCS	HP:0003581	1/2			P	HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0001659	PMID:20493459	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0000006	PMID:20493459	PCS					I	HPO:probinson[2017-06-17];HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0004942	PMID:20493459	PCS		1/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-12-05]
OMIM:614980	Congenital heart defects, multiple types, 2		HP:0032092	PMID:20493459	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-12-05]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0002918	PMID:7673400	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-05]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0000843	OMIM:145980	IEA					P	HPO:skoehler[2010-06-20]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0002150	OMIM:145980	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0003072	PMID:7673400	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-05]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0000006	PMID:7673400	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-05]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0000787	OMIM:145980	IEA					P	HPO:iea[2009-02-17]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0001733	OMIM:145980	IEA					P	HPO:iea[2009-02-17]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0003127	PMID:7673400	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-05]
OMIM:145980	Hypocalciuric hypercalcemia, familial, type I		HP:0002897	OMIM:145980	IEA					P	HPO:skoehler[2019-04-18]
OMIM:112600	Brachydactyly, type A2		HP:0010109	OMIM:112600	TAS					P	HPO:probinson[2012-06-08]
OMIM:112600	Brachydactyly, type A2		HP:0004220	OMIM:112600	TAS					P	HPO:skoehler[2015-01-28]
OMIM:112600	Brachydactyly, type A2		HP:0004691	OMIM:112600	TAS					P	HPO:skoehler[2012-11-16]
OMIM:112600	Brachydactyly, type A2		HP:0009182	PMID:19327734	PCS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0009161	PMID:19327734	PCS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0008096	OMIM:112600	TAS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0010055	OMIM:112600	TAS					P	HPO:probinson[2012-06-08]
OMIM:112600	Brachydactyly, type A2		HP:0009575	PMID:19327734	PCS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0009464	OMIM:112600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:112600	Brachydactyly, type A2		HP:0009467	PMID:19327734	PCS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0001822	PMID:19327734	PCS					P	HPO:probinson[2012-06-08]
OMIM:112600	Brachydactyly, type A2		HP:0009568	PMID:19327734	PCS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0004209	OMIM:112600	TAS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0009536	PMID:19327734	PCS					P	HPO:iea[2009-10-02]
OMIM:112600	Brachydactyly, type A2		HP:0000006	PMID:19327734	PCS					I	HPO:iea[2009-02-17]
OMIM:617251	Uncombable hair syndrome 2		HP:0002235	PMID:27866708	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617251	Uncombable hair syndrome 2		HP:0030056	PMID:27866708	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617251	Uncombable hair syndrome 2		HP:0003593	PMID:27866708	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:617251	Uncombable hair syndrome 2		HP:0001118	OMIM:617251	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617251	Uncombable hair syndrome 2		HP:0000007	PMID:27866708	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0003577	PMID:30232230	PCS		2/2			C	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0008905	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0001156	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0001250	PMID:30232230	PCS	HP:0003593	1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0003155	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0030353	PMID:30232230	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0003193	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000316	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000238	PMID:30232230	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000978	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000218	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0025336	PMID:30232230	PCS		1/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0001643	PMID:30232230	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002019	PMID:30232230	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002850	PMID:30232230	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0003049	PMID:30232230	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0003027	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002694	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000750	PMID:30232230	PCS		1/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0003025	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0011968	PMID:30232230	PCS	HP:0003593	1/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002099	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0001263	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002691	PMID:30232230	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0004691	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0006380	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0009891	PMID:30232230	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0010582	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000767	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002308	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000964	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0000007	PMID:30232230	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0001734	PMID:30232230	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0004209	PMID:30232230	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002007	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0008788	PMID:30232230	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0001631	PMID:30232230	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0034391	PMID:30232230	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:618162	Spondyloepimetaphyseal dysplasia, Krakow type		HP:0002721	PMID:30232230	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618176	Nephrotic syndrome, type 17		HP:0003774	PMID:30179222	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0003676	PMID:30179222	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0003621	PMID:30179222	PCS		3/4			C	HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0004322	PMID:30179222	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0002907	PMID:30179222	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0011463	PMID:30179222	PCS		1/4			C	HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0000097	PMID:30179222	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0000007	PMID:30179222	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0000093	PMID:30179222	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:618176	Nephrotic syndrome, type 17		HP:0012588	PMID:30179222	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-19]
OMIM:611634	Febrile convulsions, familial, 9		HP:0010849	OMIM:611634	TAS					P	HPO:iea[2012-07-16]
OMIM:611634	Febrile convulsions, familial, 9		HP:0002373	OMIM:611634	IEA					P	HPO:iea[2009-02-17]
OMIM:611634	Febrile convulsions, familial, 9		HP:0002121	OMIM:611634	TAS					P	HPO:iea[2009-02-17]
OMIM:611634	Febrile convulsions, familial, 9		HP:0000006	OMIM:611634	IEA					I	HPO:iea[2009-02-17]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0002389	PMID:33242396	PCS		1/5			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000483	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0004961	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000486	PMID:33242396	PCS		2/8			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000365	PMID:33242396	PCS		3/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000343	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0004322	PMID:33242396	PCS		6/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0012444	PMID:33242396	PCS		1/6			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0001629	PMID:33242396	PCS		3/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000518	PMID:33242396	PCS		3/8			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000958	PMID:33242396	PCS		2/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000319	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0012471	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000953	PMID:33242396	PCS		2/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000414	PMID:33242396	PCS		2/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000358	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0011829	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000252	PMID:33242396	PCS		7/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0005301	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0001263	PMID:33242396	PCS		8/8			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0031298	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000448	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000668	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000007	PMID:33242396	PCS					I	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000964	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0030051	PMID:33242396	PCS		3/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000400	PMID:33242396	PCS		2/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000543	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0002007	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0001631	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000047	PMID:33242396	PCS		2/5			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0002500	PMID:33242396	PCS		3/5			P	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000369	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000347	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0001655	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:619268	Alzahrani-Kuwahara syndrome		HP:0000742	PMID:33242396	PCS		1/9			P	HPO:probinson[2021-05-31]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0001595	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000164	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0001385	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0001773	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0001321	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000470	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000612	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0001305	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000007	OMIM:601427	TAS					I	HPO:skoehler[2015-12-30]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000824	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000851	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0002777	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0001510	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0007700	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000402	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0000765	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:601427	Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis		HP:0008736	OMIM:601427	IEA					P	HPO:iea[2009-02-17]
OMIM:221500	Deafness, neural, congenital moderate		HP:0000407	OMIM:221500	TAS	HP:0003577				P	HPO:skoehler[2010-06-18]
OMIM:221500	Deafness, neural, congenital moderate		HP:0000007	OMIM:221500	TAS					I	HPO:skoehler[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001254	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001298	OMIM:605899	IEA					P	HPO:skoehler[2015-01-27]
OMIM:605899	Glycine encephalopathy		HP:0001265	OMIM:605899	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605899	Glycine encephalopathy		HP:0001250	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0002154	OMIM:605899	TAS					P	HPO:skoehler[2010-06-18]
OMIM:605899	Glycine encephalopathy		HP:0001252	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001274	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001290	OMIM:605899	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605899	Glycine encephalopathy		HP:0100710	OMIM:605899	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605899	Glycine encephalopathy		HP:0100247	OMIM:605899	TAS					P	HPO:skoehler[2013-05-31]
OMIM:605899	Glycine encephalopathy		HP:0000737	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0000718	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0000007	OMIM:605899	IEA					I	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0000711	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0000752	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001522	OMIM:605899	TAS					C	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0003108	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001249	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001336	OMIM:605899	IEA					P	HPO:iea[2009-02-17]
OMIM:605899	Glycine encephalopathy		HP:0001347	OMIM:605899	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268100	Enhanced S-cone syndrome		HP:0000550	OMIM:268100	IEA					P	HPO:iea[2009-02-17]
OMIM:268100	Enhanced S-cone syndrome		HP:0030502	OMIM:268100	TAS					P	HPO:skoehler[2015-07-26]
OMIM:268100	Enhanced S-cone syndrome		HP:0000662	OMIM:268100	IEA					P	HPO:iea[2009-02-17]
OMIM:268100	Enhanced S-cone syndrome		HP:0012047	OMIM:268100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268100	Enhanced S-cone syndrome		HP:0040049	OMIM:268100	TAS					P	HPO:skoehler[2014-11-26]
OMIM:268100	Enhanced S-cone syndrome		HP:0000518	OMIM:268100	IEA					P	HPO:iea[2009-02-17]
OMIM:268100	Enhanced S-cone syndrome		HP:0000969	OMIM:268100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268100	Enhanced S-cone syndrome		HP:0000580	OMIM:268100	TAS					P	HPO:probinson[2017-12-22]
OMIM:268100	Enhanced S-cone syndrome		HP:0000007	OMIM:268100	IEA					I	HPO:iea[2009-02-17]
OMIM:268100	Enhanced S-cone syndrome		HP:0007773	OMIM:268100	IEA					P	HPO:iea[2009-02-17]
OMIM:153890	Macular dystrophy, fenestrated Sheen type		HP:0007754	OMIM:153890	IEA					P	HPO:iea[2009-02-17]
OMIM:153890	Macular dystrophy, fenestrated Sheen type		HP:0000006	OMIM:153890	IEA					I	HPO:iea[2009-02-17]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0001595	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0003621	PMID:33450762	PCS		1/3			C	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0000002	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0010648	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0011927	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0010938	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0010614	PMID:33450762	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0012385	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0010562	PMID:33450762	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0034363	PMID:33450762	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0002808	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0011463	PMID:33450762	PCS		2/3			C	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0009125	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0000326	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0000219	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0000422	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0001249	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0002797	PMID:33450762	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621091	Ocular pterygium-digital keloid dysplasia syndrome		HP:0000006	PMID:33450762	PCS					I	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:601341	Atrophia maculosa varioliformis cutis, familial		HP:0000007	OMIM:601341	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:601341	Atrophia maculosa varioliformis cutis, familial		HP:0007401	OMIM:601341	IEA					P	HPO:iea[2009-02-17]
OMIM:601341	Atrophia maculosa varioliformis cutis, familial		HP:0000951	OMIM:601341	IEA					P	HPO:iea[2009-02-17]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000483	PMID:28453519	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0003577	PMID:28453519	PCS		2/2			C	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000343	PMID:28453519	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000486	PMID:28453519	PCS	HP:0003577	2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0002162	PMID:28453519	PCS		1/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0001252	PMID:28453519	PCS		2/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0001270	PMID:28453519	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0012110	PMID:28453519	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000219	PMID:28453519	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000218	PMID:28453519	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0002359	PMID:28453519	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0006610	PMID:28453519	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0001500	PMID:28453519	PCS		1/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0001249	PMID:28453519	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0001265	PMID:28453519	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0001320	PMID:28453519	PCS		1/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000494	PMID:28453519	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000750	PMID:28453519	PCS		2/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0006958	PMID:28453519	PCS		1/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000649	PMID:28453519	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0011451	PMID:28453519	PCS	HP:0003577	2/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000508	PMID:28453519	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000646	PMID:28453519	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000007	PMID:28453519	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000527	PMID:28453519	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000988	PMID:28453519	PCS		1/2			P	HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0000543	PMID:28453519	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		HP:0007811	PMID:28453519	PCS		1/2			P	HPO:probinson[2022-10-09]
OMIM:620364	Combined low LDL and fibrinogen		HP:0031956	PMID:34855475	PCS					P	HPO:probinson[2023-07-16]
OMIM:620364	Combined low LDL and fibrinogen		HP:0003563	PMID:34855475	PCS					P	HPO:probinson[2023-07-16]
OMIM:620364	Combined low LDL and fibrinogen		HP:0000007	PMID:34855475	PCS					I	HPO:probinson[2023-07-16]
OMIM:620364	Combined low LDL and fibrinogen		HP:0011900	PMID:34855475	PCS					P	HPO:probinson[2023-07-16]
OMIM:607903	Hypotrichosis 6		HP:0003577	PMID:17392831	PCS		6/6			C	HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0002299	PMID:17392831	PCS		6/6			P	HPO:probinson[2014-05-24];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0000007	PMID:12705872	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0000989	PMID:17392831	PCS		6/6			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0010783	PMID:17392831	PCS		1/6			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0000653	PMID:17392831	PCS		2/6			P	HPO:probinson[2014-05-24];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0007502	PMID:17392831	PCS		1/6			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0045075	PMID:17392831	PCS		2/6			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0008070	PMID:17392831	PCS		6/6			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-08]
OMIM:607903	Hypotrichosis 6		HP:0003777	OMIM:607903	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0001562	PMID:30770808	PCS	HP:0030674				P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0003687	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0002870	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0000050	PMID:30770808	PCS			MALE		P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0001284	PMID:30770808	PCS					P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0012548	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0001270	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0000007	PMID:30770808	PCS					I	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0001558	PMID:30770808	PCS	HP:0030674				P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0001319	PMID:30770808	PCS	HP:0003623	4/4			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0001308	PMID:30770808	PCS					P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0003803	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0003701	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0003789	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0020203	PMID:30770808	PCS					P	HPO:probinson[2020-05-15]
OMIM:618823	Myopathy, congenital proximal, with minicore lesions		HP:0000028	PMID:30770808	PCS			MALE		P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0001399	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0004322	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0001250	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0001409	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0001263	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0001394	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0002097	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0000007	OMIM:210050	IEA					I	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0007029	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:210050	Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification		HP:0007238	OMIM:210050	IEA					P	HPO:iea[2009-02-17]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0001155	OMIM:246570	IEA					P	HPO:iea[2009-02-17]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0002982	OMIM:246570	IEA					P	HPO:probinson[2009-02-17]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0001849	OMIM:246570	TAS					P	HPO:probinson[2009-02-17]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0002990	OMIM:246570	TAS					P	HPO:skoehler[2009-02-17]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0001159	OMIM:246570	IEA					P	HPO:skoehler[2010-06-20]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0003745	OMIM:246570	TAS					I	HPO:skoehler[2015-12-30]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0005736	OMIM:246570	TAS					P	HPO:probinson[2009-02-17]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0000006	OMIM:246570	IEA					I	HPO:iea[2009-02-17]
OMIM:246570	Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome		HP:0009380	OMIM:246570	TAS					P	HPO:probinson[2012-07-31]
OMIM:259450	Bruck syndrome 1		HP:0000164	PMID:20696291	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0003577	PMID:20696291	PCS		2/2			C	HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0002650	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0001762	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0000364	PMID:20696291	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0003179	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0004322	OMIM:259450	TAS					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0001382	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0003273	OMIM:259450	TAS	HP:0003577				P	HPO:probinson[2012-06-13]
OMIM:259450	Bruck syndrome 1		HP:0000591	PMID:20696291	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0000939	PMID:20696291	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0006380	PMID:20696291	PCS	HP:0003577	2/2			P	HPO:probinson[2012-06-13];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0002808	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0000926	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0008422	OMIM:259450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259450	Bruck syndrome 1		HP:0000007	PMID:20696291	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0002812	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0006466	PMID:20696291	PCS	HP:0003577	2/2			P	HPO:probinson[2012-06-13];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0002659	PMID:20696291	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0000768	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:259450	Bruck syndrome 1		HP:0002987	PMID:20696291	PCS	HP:0003577	2/2			P	HPO:probinson[2012-06-13];HPO:probinson[2024-03-09]
OMIM:259450	Bruck syndrome 1		HP:0001059	OMIM:259450	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0003236	PMID:15253947	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001692	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0002460	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0003690	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0012666	PMID:15253947	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0100543	PMID:15253947	PCS		0/2		HP:0012825	P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0011463	PMID:15253947	PCS		1/2			C	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001324	PMID:10972294	PCS		10/10			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0003701	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0025717	PMID:10972294	PCS		10/10			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001423	PMID:10972294	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001249	PMID:10972294	PCS		8/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001700	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0004756	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001644	OMIM:300257	IEA		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0003546	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0003700	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0003621	PMID:15253947	PCS		1/2			C	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0002375	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0001685	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0001640	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0025075	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001761	PMID:15253947	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001263	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0011706	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001639	PMID:15253947	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001716	PMID:15253947	PCS		1/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0007210	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001635	PMID:15253947	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0000505	PMID:15253947	PCS		1/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001279	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0001678	PMID:15253947	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300257	Danon disease		HP:0003710	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:300257	Danon disease		HP:0003458	OMIM:300257	IEA					P	HPO:iea[2009-02-17]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0003621	PMID:36454683;PMID:37077559	PCS		6/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0008959	PMID:36454683;PMID:37077559	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0001288	PMID:36454683	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0001761	PMID:36454683	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0003487	PMID:36454683	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0002380	PMID:36454683	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0031993	PMID:36454683	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0003391	PMID:36454683	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0010524	PMID:36454683;PMID:37077559	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0009053	PMID:36454683;PMID:37077559	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0000726	PMID:36454683	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0007210	PMID:36454683;PMID:37077559	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0008994	PMID:36454683;PMID:37077559	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0000007	PMID:36454683	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0008997	PMID:36454683;PMID:37077559	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0003557	PMID:37077559	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620402	Neuronopathy, distal hereditary motor, autosomal recessive 9		HP:0001347	PMID:36454683	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619297	KINSSHIP syndrome		HP:0002069	PMID:33961779	PCS		9/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0003038	PMID:33961779	PCS		12/16			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000486	PMID:33961779	PCS		7/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000089	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0004322	PMID:33961779	PCS		3/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001252	PMID:33961779	PCS		11/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000085	PMID:33961779	PCS		13/17			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002020	PMID:33961779	PCS		6/16			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0012745	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0010442	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000639	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000319	PMID:33961779	PCS		3/17			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0010296	PMID:33961779	PCS		2/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000954	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000998	PMID:33961779	PCS		22/33			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000316	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000637	PMID:33961779	PCS		4/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001522	PMID:33961779	PCS		1/18			C	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001763	PMID:33961779	PCS		2/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001249	PMID:33961779	PCS		18/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000891	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0003763	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000252	PMID:33961779	PCS		11/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002673	PMID:33961779	PCS		7/18			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001263	PMID:33961779	PCS		18/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0003083	PMID:33961779	PCS		3/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0011451	PMID:33961779	PCS		9/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002827	PMID:33961779	PCS		3/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000729	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0005815	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000322	PMID:33961779	PCS		7/17			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000960	PMID:33961779	PCS		4/18			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0007359	PMID:33961779	PCS		2/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000369	PMID:33961779	PCS		3/18			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000006	PMID:33961779	PCS					I	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000687	PMID:33961779	PCS		6/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001336	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002121	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002280	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0012444	PMID:33961779	PCS		13/15			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001508	PMID:33961779	PCS		14/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0100704	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000938	PMID:33961779	PCS		6/17			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0012450	PMID:33961779	PCS		10/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000733	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001305	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000414	PMID:33961779	PCS		15/33			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002119	PMID:33961779	PCS		13/15			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000219	PMID:33961779	PCS		4/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0009765	PMID:33961779	PCS		10/18			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002714	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000179	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000212	PMID:33961779	PCS		1/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0005943	PMID:33961779	PCS		2/18			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000154	PMID:33961779	PCS		10/16			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0003027	PMID:33961779	PCS		12/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0002650	PMID:33961779	PCS		8/18			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0001285	PMID:33961779	PCS		2/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000470	PMID:33961779	PCS		2/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0200134	PMID:33961779	PCS		14/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000664	PMID:33961779	PCS		10/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000347	PMID:33961779	PCS		6/18			P	HPO:probinson[2021-07-05]
OMIM:619297	KINSSHIP syndrome		HP:0000303	PMID:33961779	PCS		2/18			P	HPO:probinson[2021-07-05]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0003819	PMID:29754768	PCS		2/5			C	HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0011463	PMID:29754768	PCS		3/5			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0001252	PMID:29754768	PCS		1/3		HP:0012828	P	HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0002151	PMID:29754768	PCS		3/5			P	HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0003593	PMID:29754768	PCS		1/5			C	HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0000007	PMID:29754768	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0002092	PMID:29754768	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0012664	PMID:29754768	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0001522	PMID:29754768	PCS		1/5			C	HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0001644	PMID:29754768	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-03]
OMIM:618189	Cardiomyopathy, dilated, 2C		HP:0003623	PMID:29754768	PCS		1/5			C	HPO:probinson[2022-07-03]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0008936	PMID:36718090	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0002015	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0001344	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0002650	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0002144	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0000750	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0004322	PMID:36718090	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0031936	PMID:36718090	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0001332	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0001052	PMID:36718090	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0001250	PMID:36718090	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0002020	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0002064	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0003593	PMID:36718090	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0001508	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0034353	PMID:36718090	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0000407	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0002307	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0000256	PMID:36718090	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0001249	PMID:36718090	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620416	Spastic paraplegia 90A, autosomal dominant		HP:0000006	PMID:36718090	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0004325	OMIM:300243	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0002487	PMID:18342287	PCS		5/11			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0002300	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000486	PMID:18342287	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001272	PMID:18342287	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001371	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001250	PMID:18342287	PCS		11/11			P	HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001252	OMIM:300243	TAS					P	HPO:skoehler[2014-11-26]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000020	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001251	PMID:18342287	PCS		11/11			P	HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001290	OMIM:300243	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0040082	PMID:18342287	PCS					P	HPO:skoehler[2014-11-27];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0011182	PMID:18342287	PCS		11/11			P	HPO:probinson[2020-12-10];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0006794	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000774	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0007207	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001760	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000275	OMIM:300243	TAS					P	HPO:probinson[2012-05-01]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0003202	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0002015	PMID:18342287	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000252	PMID:18342287	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001344	PMID:18342287	PCS		11/11	MALE		P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0003189	OMIM:300243	TAS					P	HPO:probinson[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000574	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0002078	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000276	OMIM:300243	TAS					P	HPO:probinson[2012-05-01]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000194	PMID:18342287	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0012736	PMID:18342287	PCS		11/11			P	HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001181	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001419	PMID:18342287	PCS					I	HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0002607	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000602	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0002529	OMIM:300243	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0002307	PMID:18342287	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-12-10]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000400	OMIM:300243	IEA					P	HPO:iea[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0000303	OMIM:300243	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300243	Intellectual developmental disorder, X-linked syndromic, Christianson type		HP:0001238	OMIM:300243	IEA					P	HPO:skoehler[2010-06-20]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0003621	PMID:39468830	PCS		4/40			C	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0003431	PMID:39468830	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0000365	PMID:39468830	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0003387	PMID:39468830	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0003487	PMID:39468830	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0001288	PMID:39468830	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0001098	PMID:39468830	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0031993	PMID:39468830	PCS		7/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0033206	PMID:39468830	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0011449	PMID:39468830	PCS		2/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0011448	PMID:39468830	PCS		7/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0012078	PMID:39468830	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0007083	PMID:39468830	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0007340	PMID:39468830	PCS		7/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0000649	PMID:39468830	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0011463	PMID:39468830	PCS		2/10			C	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0011462	PMID:39468830	PCS		4/40			C	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0001427	PMID:39468830	PCS					I	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0001258	PMID:39468830	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0003448	PMID:39468830	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:500018	Mitochondrial spastic paraplegia		HP:0006886	PMID:39468830	PCS		8/10			P	ORCID:0000-0002-0736-9199[2025-09-24]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0003026	OMIM:250460	IEA					P	HPO:iea[2009-02-17]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0001595	PMID:11940090	PCS		0/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0004322	PMID:11940090	PCS		2/2			P	HPO:probinson[2022-08-22];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0003025	PMID:11940090	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0002970	PMID:11940090	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0001382	PMID:11940090	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0010049	PMID:11940090	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0031367	PMID:11940090	PCS		2/2			P	HPO:probinson[2022-08-22];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0100255	PMID:11940090	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0000925	PMID:11940090	PCS		0/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0011463	PMID:11940090	PCS		2/2			C	HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0010230	PMID:11940090	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0001999	PMID:11940090	PCS		0/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0000007	PMID:11940090	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0006028	OMIM:250460	IEA					P	HPO:iea[2009-02-17]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0002721	PMID:11940090	PCS		0/2			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-08-22]
OMIM:250460	Metaphyseal dysplasia without hypotrichosis		HP:0002644	PMID:11940090	PCS		0/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:314550	Vesicoureteral reflux, X-linked		HP:0000076	OMIM:314550	IEA					P	HPO:iea[2009-02-17]
OMIM:314550	Vesicoureteral reflux, X-linked		HP:0001417	OMIM:314550	IEA					I	HPO:iea[2009-02-17]
OMIM:620370	RECON progeroid syndrome		HP:0008407	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0004322	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000463	PMID:35025765	PCS		2/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0001097	PMID:35025765	PCS		2/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0003593	PMID:35025765	PCS		3/3			C	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0033505	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000958	PMID:35025765	PCS		3/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0002719	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000418	PMID:35025765	PCS		3/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000319	PMID:35025765	PCS		3/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0001903	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0008551	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000678	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0025337	PMID:35025765	PCS		2/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0009623	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000311	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000696	PMID:35025765	PCS		2/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0001007	PMID:35025765	PCS		2/6			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0005328	PMID:35025765	PCS		3/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0007646	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0001166	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0003202	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000252	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000992	PMID:35025765	PCS		3/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0010759	PMID:35025765	PCS		3/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000233	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000430	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0001382	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0009907	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000490	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0032524	PMID:35025765	PCS		3/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0032152	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0040189	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000426	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000007	PMID:35025765	PCS					I	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0001510	PMID:35025765	PCS		2/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0001873	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:620370	RECON progeroid syndrome		HP:0000963	PMID:35025765	PCS		1/3			P	HPO:probinson[2023-07-08]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000286	PMID:11977162;PMID:3443553	PCS		13/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000486	OMIM:613792	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000365	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0002023	PMID:3443553	PCS		1/19			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000243	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0004322	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001250	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001252	PMID:11977162;PMID:3443553	PCS		10/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0002020	PMID:11977162	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001845	PMID:11977162	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000316	PMID:11977162;PMID:3443553	PCS		9/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0008897	PMID:3443553	PCS		17/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000278	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001249	PMID:3443553	PCS		17/17			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0002553	OMIM:613792	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0005469	PMID:3443553	PCS		7/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000252	PMID:3443553	PCS		14/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0002353	PMID:3443553	PCS		7/19			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001344	OMIM:613792	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0011968	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001263	PMID:11977162	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001182	OMIM:613792	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0100259	PMID:3443553	PCS		9/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001257	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000960	PMID:11977162;PMID:3443553	PCS		7/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000325	PMID:3443553	PCS		7/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000369	PMID:11977162;PMID:3443553	PCS		13/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000248	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000006	OMIM:613792	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000582	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0004467	PMID:3443553	PCS		5/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0003577	PMID:3443553	PCS					C	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000343	PMID:11977162;PMID:3443553	PCS		12/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000463	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000581	PMID:11977162	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0012210	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000414	PMID:11977162	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0006695	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0030680	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000219	PMID:11977162	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0009765	OMIM:613792	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000218	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0002714	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001104	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000455	OMIM:613792	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000396	PMID:11977162	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000431	PMID:11977162	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000233	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0005487	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0005280	PMID:11977162	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001518	PMID:3443553	PCS		9/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000508	PMID:11977162;PMID:3443553	PCS		18/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000629	OMIM:613792	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000426	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000664	PMID:3443553	PCS		8/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001511	PMID:11977162	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000268	PMID:3443553	PCS		6/19			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0001510	PMID:11977162	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000347	PMID:11977162;PMID:3443553	PCS		10/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:613792	Chromosome 3pter-p25 deletion syndrome		HP:0000028	OMIM:613792	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0002311	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0003401	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0000651	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0000716	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0000020	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0003581	OMIM:126200	TAS					C	HPO:probinson[2022-08-15]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0000019	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0000712	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0001426	OMIM:126200	IEA					I	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0001324	OMIM:126200	TAS					P	HPO:probinson[2012-04-11]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0001257	OMIM:126200	IEA					P	HPO:iea[2009-02-17]
OMIM:126200	Multiple sclerosis, susceptibility to		HP:0007305	OMIM:126200	TAS					P	HPO:probinson[2012-04-11]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0006846	PMID:34483339	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001332	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0003572	PMID:34483339	PCS		2/3			P	HPO:probinson[2023-06-14];HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0002385	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0003593	PMID:34954817	PCS		1/1			C	HPO:probinson[2023-06-14];HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001508	PMID:34483339;PMID:34954817	PCS		4/6			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001903	PMID:34483339	PCS		2/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001987	PMID:34483339	PCS		3/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0008358	PMID:34483339	PCS		3/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0500149	PMID:34483339	PCS		2/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0007325	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001249	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0003623	PMID:34483339	PCS		3/3			C	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0003128	PMID:34483339;PMID:34954817	PCS		4/6			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0003348	PMID:34483339	PCS		3/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0002015	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001344	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0005961	PMID:34483339	PCS		2/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0002497	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0011968	PMID:34483339	PCS		3/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0002154	PMID:34483339	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001263	PMID:34483339;PMID:34954817	PCS		3/6			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0002151	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0001285	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0100021	PMID:34954817	PCS		1/3			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0003218	PMID:34483339	PCS		2/2			P	HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0000006	PMID:34483339	PCS					I	HPO:probinson[2023-06-14];HPO:probinson[2023-06-14]
OMIM:620358	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A		HP:0002028	PMID:34483339	PCS		2/3			P	HPO:probinson[2023-06-14]
OMIM:311400	Paine syndrome		HP:0006955	OMIM:311400	TAS					P	HPO:skoehler[2012-09-10]
OMIM:311400	Paine syndrome		HP:0000252	OMIM:311400	IEA					P	HPO:iea[2009-02-17]
OMIM:311400	Paine syndrome		HP:0001264	OMIM:311400	IEA					P	HPO:iea[2009-02-17]
OMIM:311400	Paine syndrome		HP:0001321	OMIM:311400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311400	Paine syndrome		HP:0002123	OMIM:311400	IEA					P	HPO:iea[2009-02-17]
OMIM:311400	Paine syndrome		HP:0001417	OMIM:311400	IEA					I	HPO:iea[2009-02-17]
OMIM:122700	Coumarin resistance		HP:0001871	OMIM:122700	IEA					P	HPO:iea[2009-02-17]
OMIM:122700	Coumarin resistance		HP:0000006	OMIM:122700	IEA					I	HPO:iea[2009-02-17]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000286	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002540	PMID:23383720	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000486	PMID:28100473	PCS		7/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000243	PMID:26647312;PMID:24044690;PMID:23383720	PCS		2/7			P	HPO:skoehler[2015-08-29];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001250	PMID:26647312;PMID:28100473	PCS		4/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001252	PMID:26647312;PMID:28100473	PCS		14/15			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0003196	PMID:26647312;PMID:23383720	PCS		4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002020	PMID:23383720	PCS		2/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001290	PMID:23383720	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0011410	PMID:28100473	PCS	HP:0003577	9/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0045074	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0006191	PMID:23383720	PCS		3/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0011220	PMID:26647312;PMID:28100473;PMID:23383720	PCS		4/19			P	HPO:probinson[2021-10-03];HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000717	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000316	PMID:24044690;PMID:28100473;PMID:23383720	PCS		4/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000239	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000678	PMID:28100473	PCS		2/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001522	PMID:23383720	PCS		1/4			C	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001763	PMID:28100473	PCS		1/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000278	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001007	PMID:28100473;PMID:23383720	PCS		2/16			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001249	PMID:26647312;PMID:28100473;PMID:23383720	PCS		16/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001601	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000358	PMID:26647312;PMID:24044690;PMID:28100473;PMID:23383720	PCS		4/20			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001188	PMID:23383720	PCS		2/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002553	PMID:26647312;PMID:23383720	PCS		5/7			P	HPO:skoehler[2015-08-29];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000494	PMID:26647312;PMID:28100473	PCS		8/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000252	PMID:26647312;PMID:24044690;PMID:23383720	PCS		3/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001344	PMID:26647312;PMID:24044690;PMID:23383720	PCS		5/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000574	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000452	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002079	PMID:26647312	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000331	PMID:26647312	PCS		2/3			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0011968	PMID:26647312;PMID:28100473	PCS		12/15			P	HPO:skoehler[2015-08-29];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000490	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001263	PMID:26647312;PMID:24044690	PCS		4/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0033454	PMID:23383720	PCS	HP:0003593	3/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0100023	PMID:28100473	PCS		3/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000729	PMID:24044690;PMID:28100473	PCS		10/13			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0011330	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000527	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000520	PMID:26647312	PCS		0/3			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000006	PMID:23383720	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000369	PMID:26647312;PMID:23383720	PCS		4/7			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001276	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0030799	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000340	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000582	PMID:24044690	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000463	PMID:26647312;PMID:24044690;PMID:23383720	PCS		5/8			P	HPO:skoehler[2015-08-29];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000540	PMID:26647312;PMID:23383720	PCS		2/7			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002000	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0008070	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001508	PMID:26647312;PMID:24044690	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002719	PMID:26647312	PCS		1/3			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0009487	PMID:26647312;PMID:23383720	PCS		3/7			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0007068	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000733	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000219	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000218	PMID:28100473;PMID:23383720	PCS		11/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000455	PMID:28100473	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000212	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002558	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001623	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000154	PMID:28100473	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001166	PMID:28100473	PCS		2/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0006956	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001561	PMID:28100473	PCS	HP:0011461	1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000750	PMID:28100473	PCS		12/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002650	PMID:28100473	PCS		1/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000431	PMID:26647312	PCS		1/3			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0031936	PMID:28100473	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000232	PMID:28100473	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000430	PMID:24044690;PMID:23383720	PCS		2/5			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002013	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000272	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0011344	PMID:23383720	PCS		4/4			P	HPO:skoehler[2015-08-29];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0005280	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0009276	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001519	PMID:28100473	PCS		3/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000826	PMID:26647312	PCS		1/2			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0040288	PMID:26647312	PCS		3/3			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000629	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000426	PMID:28100473	PCS		3/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0100716	PMID:24044690	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001511	PMID:26647312	PCS	HP:0011461	2/3			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000664	PMID:28100473	PCS		2/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0001510	PMID:28100473	PCS					P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000028	PMID:23383720	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0002566	PMID:28100473	PCS		1/12			P	HPO:probinson[2021-10-03]
OMIM:615485	Bainbridge-Ropers syndrome		HP:0000347	PMID:28100473	PCS		2/12			P	HPO:probinson[2021-10-03]
OMIM:211400	Bronchiectasis with or without elevated sweat chloride 1		HP:0002110	OMIM:211400	TAS					P	HPO:skoehler[2010-06-18]
OMIM:211400	Bronchiectasis with or without elevated sweat chloride 1		HP:0012092	PMID:16207733	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:211400	Bronchiectasis with or without elevated sweat chloride 1		HP:0012236	OMIM:211400	TAS		HP:0040283			P	HPO:skoehler[2013-03-31]
OMIM:211400	Bronchiectasis with or without elevated sweat chloride 1		HP:0000006	PMID:16207733	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-08]
OMIM:211400	Bronchiectasis with or without elevated sweat chloride 1		HP:0004469	OMIM:211400	TAS					P	HPO:skoehler[2010-06-18]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0003676	PMID:28007905	PCS					C	HPO:skoehler[2013-11-18];HPO:probinson[2024-03-15]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000640	PMID:28007905;PMID:23359680	PCS		6/6			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001310	OMIM:615491	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002486	PMID:28007905;PMID:23359680	PCS		2/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001272	PMID:28007905;PMID:23359680	PCS		4/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001371	OMIM:615491	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001251	PMID:23359680	PCS		3/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002380	PMID:28007905	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002061	PMID:28007905;PMID:23359680	PCS		5/6			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002180	OMIM:615491	IEA					P	HPO:skoehler[2015-01-27]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002080	PMID:28007905	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0007141	PMID:28007905	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0007663	PMID:28007905	PCS		3/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000597	PMID:28007905	PCS		1/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001763	OMIM:615491	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002599	PMID:28007905;PMID:23359680	PCS		4/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001249	PMID:28007905	PCS		0/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001347	PMID:28007905;PMID:23359680	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000572	PMID:28007905;PMID:23359680	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002059	PMID:23359680	PCS		3/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002411	PMID:28007905	PCS		1/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0003621	PMID:28007905	PCS		3/3			C	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0003487	PMID:28007905;PMID:23359680	PCS		5/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001761	PMID:28007905	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0006938	PMID:28007905	PCS		3/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002495	PMID:23359680	PCS		3/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002174	PMID:28007905	PCS		1/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002273	OMIM:615491	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0031993	PMID:28007905;PMID:23359680	PCS		1/6			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0034008	PMID:23359680	PCS		3/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0011448	OMIM:615491	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0010831	PMID:28007905;PMID:23359680	PCS		6/6			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000529	PMID:28007905	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-15]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000649	PMID:28007905	PCS		0/2			P	HPO:probinson[2024-03-15]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000007	PMID:23359680	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000648	PMID:28007905;PMID:23359680	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0002505	PMID:28007905;PMID:23359680	PCS		6/6			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000768	PMID:28007905	PCS		2/3			P	HPO:probinson[2022-10-09]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0001258	OMIM:615491	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615491	Spastic paraplegia 79, autosomal recessive		HP:0000545	OMIM:615491	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0003577	PMID:25434004	PCS		3/11			C	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0003621	PMID:25434004	PCS		1/11			C	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0011968	PMID:25434004	PCS		1/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001250	PMID:25434004	PCS		2/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001263	PMID:25434004	PCS		4/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001252	PMID:25434004	PCS		4/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0002151	PMID:25434004	PCS		12/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0003593	PMID:25434004	PCS		3/11			C	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0011675	PMID:25434004	PCS		1/12			P	HPO:skoehler[2015-02-22]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0011923	PMID:25434004	PCS		9/10			P	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001508	PMID:25434004	PCS		1/12			P	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0011463	PMID:25434004	PCS		3/11			C	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001639	PMID:25434004	PCS		7/11			P	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0000007	PMID:25434004	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-10]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001635	PMID:25434004	PCS		1/12			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0000505	PMID:25434004	PCS		1/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0008347	PMID:25434004	PCS		8/10			P	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001511	PMID:25434004	PCS		1/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0003688	PMID:25434004	PCS		4/4			P	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0003128	PMID:25434004	PCS		12/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0003623	PMID:25434004	PCS		1/11			C	HPO:probinson[2023-06-05]
OMIM:616198	Combined oxidative phosphorylation deficiency 23		HP:0001644	PMID:25434004	PCS		1/11			P	HPO:probinson[2023-06-05]
OMIM:607095	Anauxetic dysplasia 1		HP:0001650	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0003015	PMID:11370632	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0003510	PMID:11370632	PCS		3/4			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0003577	PMID:11370632	PCS		1/2			C	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001377	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0008905	PMID:11370632	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001773	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001552	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001156	OMIM:607095	TAS					P	HPO:skoehler[2014-11-26]
OMIM:607095	Anauxetic dysplasia 1		HP:0002341	PMID:11370632	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0003273	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001252	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0002680	OMIM:607095	IEA		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0010585	OMIM:607095	IEA					P	HPO:iea[2009-02-17]
OMIM:607095	Anauxetic dysplasia 1		HP:0009381	OMIM:607095	TAS					P	HPO:probinson[2012-06-10]
OMIM:607095	Anauxetic dysplasia 1		HP:0002938	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0000316	OMIM:607095	IEA					P	HPO:iea[2009-02-17]
OMIM:607095	Anauxetic dysplasia 1		HP:0003308	OMIM:607095	IEA					P	HPO:iea[2009-02-17]
OMIM:607095	Anauxetic dysplasia 1		HP:0000158	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001249	PMID:11370632	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0004279	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001382	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001263	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0000691	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0000470	OMIM:607095	IEA					P	HPO:iea[2009-02-17]
OMIM:607095	Anauxetic dysplasia 1		HP:0000946	OMIM:607095	IEA					P	HPO:iea[2009-02-17]
OMIM:607095	Anauxetic dysplasia 1		HP:0034198	PMID:11370632	PCS		1/2			C	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0000926	PMID:11370632	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0000668	OMIM:607095	IEA					P	HPO:iea[2009-02-17]
OMIM:607095	Anauxetic dysplasia 1		HP:0000007	PMID:16252239	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0000307	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001511	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0002942	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0002987	PMID:11370632	PCS		2/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001216	PMID:11370632	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0000303	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0003414	PMID:11370632	PCS		1/2			P	HPO:probinson[2022-08-11]
OMIM:607095	Anauxetic dysplasia 1		HP:0001831	OMIM:607095	TAS					P	HPO:probinson[2012-06-10]
OMIM:300519	Martin-Probst syndrome		HP:0000286	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0004322	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000083	PMID:11073537	PCS	HP:0003596	1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000041	PMID:11073537	PCS		1/3			P	HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0001009	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000316	PMID:11073537	PCS		1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0006610	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0002557	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000179	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0001249	PMID:11073537	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000154	PMID:11073537	PCS		1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000054	PMID:11073537	PCS		1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000252	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000431	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000272	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0045025	PMID:11073537	PCS		2/3			P	HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000093	PMID:11073537	PCS	HP:0003621	1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0001419	PMID:11073537	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000506	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000407	PMID:11073537	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0001537	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000821	PMID:11073537	PCS		1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000689	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000048	PMID:11073537	PCS	HP:0003577	1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0001876	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000545	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000347	PMID:11073537	PCS		2/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000369	PMID:11073537	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:300519	Martin-Probst syndrome		HP:0000028	PMID:11073537	PCS		1/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2020-10-20]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0007208	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0004336	PMID:10802647	PCS					P	HPO:probinson[2022-09-02]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0010628	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0001762	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0002650	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0003431	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0006958	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0003693	OMIM:601382	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0002460	OMIM:601382	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0001270	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0000007	PMID:10802647	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0002936	OMIM:601382	TAS					P	HPO:skoehler[2013-04-02]
OMIM:601382	Charcot-Marie-Tooth disease, type 4B1		HP:0003701	OMIM:601382	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0003015	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0003510	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000582	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0002188	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0008905	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0001596	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0002120	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0001371	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0001250	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0012368	OMIM:215100	TAS					P	HPO:skoehler[2013-10-22]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0010571	PMID:12325024	PCS	HP:0011463				P	HPO:probinson[2021-07-05]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000519	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0001525	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0001249	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0002751	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000175	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000252	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0005841	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000272	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0002093	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0005280	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0010655	OMIM:215100	TAS					P	HPO:probinson[2012-05-27]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0008064	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000407	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000007	PMID:9090381	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0003417	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0002007	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0001257	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:215100	Rhizomelic chondrodysplasia punctata, type 1		HP:0000347	OMIM:215100	IEA					P	HPO:iea[2009-02-17]
OMIM:134610	Familial Mediterranean fever, AD		HP:0002102	PMID:14679589	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0002586	PMID:14679589	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0003621	PMID:14679589	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0001055	PMID:14679589	PCS		4/5			P	HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0005764	PMID:14679589	PCS		5/5		HP:0025303	P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0000083	PMID:14679589	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0000093	PMID:14679589	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0002829	PMID:14679589	PCS		5/5		HP:0025303	P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0001917	PMID:14679589	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0001954	PMID:14679589	PCS	HP:0003621	5/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0100749	PMID:14679589	PCS				HP:0025303	P	HPO:skoehler[2015-01-04];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0000006	PMID:10787449	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:134610	Familial Mediterranean fever, AD		HP:0002027	PMID:14679589	PCS				HP:0025303	P	HPO:iea[2009-02-17];HPO:probinson[2020-10-26]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:0005974	PMID:8751852	PCS				HP:0012828	P	HPO:iea[2012-05-05];HPO:probinson[2020-07-21]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:0002919	OMIM:245050	IEA					P	HPO:iea[2009-02-17]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:0002013	OMIM:245050	IEA					P	HPO:iea[2009-02-17]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:6000361	PMID:11757586	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:0040155	PMID:8751852	PCS					P	HPO:probinson[2020-07-21]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:0000007	PMID:10964512	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-07-21]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:0002789	OMIM:245050	IEA					P	HPO:iea[2009-02-17]
OMIM:245050	Succinyl CoA:3-oxoacid CoA transferase deficiency		HP:0003623	PMID:8751852	PCS					C	HPO:probinson[2020-07-21]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001694	PMID:27071622;OMIM:265380	PCS		12/47			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0030732	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002023	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002023	PMID:27071622	PCS		3/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002101	OMIM:265380	TAS					P	HPO:skoehler[2014-09-21]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0003396	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001252	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0011611	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0011611	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0410030	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0410030	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0010444	PMID:19500772	PCS					P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0010882	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0033208	PMID:27071622;PMID:19500772	PCS		44/51			P	HPO:probinson[2021-05-05];HPO:probinson[2020-12-07]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0012304	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000913	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000913	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001647	PMID:27071622;PMID:19500772	PCS	HP:0003577	4/51			P	HPO:probinson[2020-10-02];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000316	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001643	PMID:27071622;PMID:19500772	PCS		22/51			P	HPO:probinson[2021-05-05];HPO:skoehler[2010-06-20];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000476	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000278	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001540	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000175	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000175	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0005301	PMID:27071622	PCS		3/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002032	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000490	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001263	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0010955	PMID:19500772	PCS		2/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002190	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0033186	PMID:27071622;PMID:19500772	PCS		44/51			P	HPO:probinson[2020-10-13];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0011571	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002308	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0004927	PMID:27071622;PMID:19500772	PCS		2/51			P	HPO:probinson[2020-10-02];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001734	PMID:19500772	PCS	HP:0003577	2/14			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001734	PMID:27071622	PCS		4/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001539	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0003316	PMID:19500772	PCS	HP:0003577	2/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0003316	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000047	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000006	PMID:19500772	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-01]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000248	PMID:27071622;PMID:19500772	PCS		2/51			P	HPO:probinson[2021-05-05];HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000369	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000126	PMID:27071622;PMID:19500772	PCS		13/51			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001655	PMID:27071622	PCS	HP:0003623	3/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002245	PMID:19500772	PCS		1/14			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002202	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0010946	PMID:19500772	PCS		3/14			P	HPO:probinson[2020-10-02];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001195	PMID:19500772	PCS	HP:0003577	3/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001195	PMID:27071622	PCS		7/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001790	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0004383	PMID:19500772	PCS	HP:0003577	2/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0004383	PMID:27071622	PCS		5/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001629	PMID:27071622	PCS		5/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001746	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001746	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0006695	PMID:27071622	PCS		6/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000813	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002119	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-01];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0004415	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001667	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002575	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001561	PMID:27071622	PCS		1/37			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000474	PMID:27071622	PCS		1/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000072	PMID:27071622;PMID:19500772	PCS		6/51			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001680	PMID:27071622	PCS	HP:0003577	3/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0010773	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002092	PMID:19500772	PCS		1/14			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0030889	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001636	PMID:19500772	PCS	HP:0003577	1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001636	PMID:27071622	PCS		2/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0006521	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0003811	PMID:19500772	PCS		10/13			C	HPO:probinson[2012-07-27];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001631	PMID:19500772	PCS	HP:0003577	2/14			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0001631	PMID:27071622	PCS		4/37			P	HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002247	PMID:27071622;PMID:19500772	PCS		4/51			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002566	PMID:27071622;PMID:19500772	PCS		11/51			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-02];HPO:probinson[2021-05-05]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0000347	PMID:19500772	PCS		1/14			P	HPO:probinson[2020-10-02]
OMIM:265380	Alveolar capillary dysplasia with misalignment of pulmonary veins		HP:0002643	PMID:19500772	PCS	HP:0003623				P	HPO:probinson[2020-10-02]
OMIM:136760	Frontonasal dysplasia 1		HP:0000286	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000384	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0004423	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0005258	OMIM:136760	TAS					P	HPO:probinson[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0001156	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000161	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0002000	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0001274	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000518	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000316	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0007541	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0002738	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0006992	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0009466	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0030084	OMIM:136760	TAS					P	HPO:skoehler[2014-09-21]
OMIM:136760	Frontonasal dysplasia 1		HP:0003745	OMIM:136760	IEA					I	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0001566	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000455	OMIM:136760	TAS					P	HPO:probinson[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0001249	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0006931	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000456	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000431	OMIM:136760	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0001162	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0011803	OMIM:136760	IEA					P	HPO:skoehler[2018-10-08]
OMIM:136760	Frontonasal dysplasia 1		HP:0012385	OMIM:136760	TAS					P	HPO:skoehler[2013-10-22]
OMIM:136760	Frontonasal dysplasia 1		HP:0009099	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0009473	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000508	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000327	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000349	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0001636	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000568	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000007	OMIM:136760	TAS					I	HPO:skoehler[2015-12-30]
OMIM:136760	Frontonasal dysplasia 1		HP:0000405	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000369	OMIM:136760	TAS					P	HPO:skoehler[2009-02-17]
OMIM:136760	Frontonasal dysplasia 1		HP:0000589	OMIM:136760	IEA					P	HPO:iea[2009-02-17]
OMIM:616199	Polyglucosan body myopathy 2		HP:0008946	PMID:25272951	PCS		2/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0030237	PMID:25272951	PCS		1/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0003236	PMID:25272951	PCS		1/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0003596	PMID:25272951	PCS		1/7			C	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0001288	PMID:25272951	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0003584	PMID:25272951	PCS		3/7			C	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0011727	PMID:25272951	PCS		1/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0002460	PMID:25272951	PCS		1/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0034766	PMID:26652229	PCS		5/5			P	HPO:probinson[2023-06-05]
OMIM:616199	Polyglucosan body myopathy 2		HP:0100299	PMID:25272951	PCS		7/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0010546	PMID:25272951	PCS		3/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0011463	PMID:25272951	PCS		1/7			C	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0011462	PMID:25272951	PCS		2/7			C	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0003749	PMID:25272951	PCS		6/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0000007	PMID:25272951	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0003547	PMID:25272951	PCS		4/7			P	HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0003325	PMID:25272951	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:616199	Polyglucosan body myopathy 2		HP:0003677	PMID:25272951	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0003477	OMIM:615490	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0002136	OMIM:615490	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0002540	OMIM:615490	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0001762	OMIM:615490	TAS					P	HPO:skoehler[2015-07-26]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0003431	PMID:23562820	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0031936	PMID:23562820	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0001761	PMID:23562820	PCS		1/1			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0003199	OMIM:615490	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0001252	PMID:23562820	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0001284	PMID:23562820	PCS		1/1			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0003593	PMID:23562820	PCS		1/1			C	HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0003380	OMIM:615490	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0002093	OMIM:615490	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0006380	OMIM:615490	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0040078	OMIM:615490	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0000007	PMID:23562820	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0002779	OMIM:615490	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0001605	OMIM:615490	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0001324	PMID:23562820	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-21]
OMIM:615490	Charcot-Marie-Tooth disease, axonal, type 2R		HP:0008954	PMID:23562820	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001331	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0002389	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0005257	OMIM:208150	TAS					P	HPO:probinson[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0100490	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000160	PMID:25537362	PCS		3/11			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0003199	PMID:25537362	PCS		6/10			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0003273	PMID:25537362	PCS		10/13			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0012745	OMIM:208150	TAS					P	HPO:skoehler[2014-03-24]
OMIM:208150	Fetal akinesia deformation sequence		HP:0003070	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000437	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000316	PMID:25537362	PCS		9/12			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0003826	OMIM:208150	TAS					C	HPO:probinson[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000238	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000476	PMID:25537362	PCS		1/6			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000358	OMIM:208150	TAS					P	HPO:probinson[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0003700	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000175	PMID:25537362	PCS		0/13			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0010880	PMID:25537362	PCS		1/6			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000007	PMID:25537362	PCS					I	HPO:iea[2012-07-25];HPO:probinson[2023-01-27]
OMIM:208150	Fetal akinesia deformation sequence		HP:0002705	OMIM:208150	TAS					P	HPO:skoehler[2015-12-30]
OMIM:208150	Fetal akinesia deformation sequence		HP:0006266	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000520	OMIM:208150	TAS					P	HPO:probinson[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000883	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000369	PMID:25537362	PCS		8/12			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0034391	PMID:25537362	PCS		5/12			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0003577	PMID:25537362	PCS		14/14			C	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000343	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0002089	PMID:25537362	PCS		13/13			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000581	OMIM:208150	TAS					P	HPO:probinson[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001196	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001790	PMID:25537362	PCS		1/6			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001193	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0009487	OMIM:208150	TAS					P	HPO:skoehler[2015-12-30]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001989	PMID:25537362	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000218	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001622	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001561	PMID:25537362	PCS		11/13			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001762	PMID:25537362	PCS		3/5			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001321	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0003100	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000470	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001838	PMID:25537362	PCS		1/12			P	HPO:probinson[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001518	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000506	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000508	OMIM:208150	IEA					P	HPO:iea[2012-07-25]
OMIM:208150	Fetal akinesia deformation sequence		HP:0002803	PMID:25537362	PCS		5/5			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0002804	OMIM:208150	IEA					P	HPO:skoehler[2015-01-19]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001558	PMID:25537362	PCS		6/7			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001239	PMID:25537362	PCS		12/12			P	HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0001511	PMID:25537362	PCS		2/12			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000028	PMID:25537362	PCS		7/7			P	HPO:iea[2012-07-25];HPO:probinson[2023-01-28]
OMIM:208150	Fetal akinesia deformation sequence		HP:0000347	PMID:25537362	PCS		8/13			P	HPO:probinson[2012-07-25];HPO:probinson[2023-01-28]
OMIM:241550	Hypoplastic left heart syndrome		HP:0001650	PMID:15690347	TAS		32/413			P	HPO:nvasilevsky[2019-03-12]
OMIM:241550	Hypoplastic left heart syndrome		HP:0001680	PMID:15690347	TAS		32/413			P	HPO:nvasilevsky[2019-03-12]
OMIM:241550	Hypoplastic left heart syndrome		HP:0004383	PMID:15690347;OMIM:241550	TAS		42/423			P	HPO:nvasilevsky[2019-03-12];HPO:iea[2009-02-17]
OMIM:241550	Hypoplastic left heart syndrome		HP:0001426	PMID:1248182	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:241550	Hypoplastic left heart syndrome		HP:0010983	PMID:15690347	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:241550	Hypoplastic left heart syndrome		HP:0000007	PMID:5111754	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:236900	Hydroxylysinuria		HP:0002123	OMIM:236900	IEA					P	HPO:iea[2009-02-17]
OMIM:236900	Hydroxylysinuria		HP:0003297	OMIM:236900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236900	Hydroxylysinuria		HP:0000007	OMIM:236900	IEA					I	HPO:iea[2009-02-17]
OMIM:236900	Hydroxylysinuria		HP:0001249	OMIM:236900	IEA					P	HPO:iea[2009-02-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0001397	OMIM:261680	IEA					P	HPO:iea[2009-02-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0002059	OMIM:261680	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0002353	OMIM:261680	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0001399	PMID:26971250	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0003572	OMIM:261680	IEA					P	HPO:skoehler[2018-10-08]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0001250	OMIM:261680	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0001263	OMIM:261680	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0002240	OMIM:261680	IEA					P	HPO:skoehler[2018-10-08]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0003593	PMID:26971250	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-13]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0003162	OMIM:261680	IEA					P	HPO:skoehler[2018-10-08]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0002480	OMIM:261680	IEA					P	HPO:skoehler[2018-10-08]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0031964	PMID:26971250	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0002919	OMIM:261680	IEA					P	HPO:skoehler[2018-10-08]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:6000619	PMID:107509	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0031141	PMID:26971250	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0000007	PMID:26971250	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0001943	PMID:26971250	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0000799	OMIM:261680	IEA					P	HPO:iea[2009-02-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0005959	OMIM:261680	IEA					P	HPO:iea[2009-02-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0000648	OMIM:261680	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0000961	OMIM:261680	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0002104	OMIM:261680	TAS				HP:0025303	P	HPO:skoehler[2013-06-06]
OMIM:261680	Phosphoenolpyruvate carboxykinase deficiency, cytosolic		HP:0003128	PMID:26971250	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-13]
OMIM:300518	Intellectual developmental disorder, X-linked 82		HP:0002353	OMIM:300518	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300518	Intellectual developmental disorder, X-linked 82		HP:0002650	OMIM:300518	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300518	Intellectual developmental disorder, X-linked 82		HP:0001250	OMIM:300518	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300518	Intellectual developmental disorder, X-linked 82		HP:0001419	OMIM:300518	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300518	Intellectual developmental disorder, X-linked 82		HP:0002808	OMIM:300518	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300518	Intellectual developmental disorder, X-linked 82		HP:0000729	OMIM:300518	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300518	Intellectual developmental disorder, X-linked 82		HP:0001249	OMIM:300518	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0003202	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0003236	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0003676	OMIM:616827	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0001762	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0002273	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0003560	OMIM:616827	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0011463	PMID:25589244	PCS					C	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0008981	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0009025	OMIM:616827	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0000007	PMID:25589244	PCS					I	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0030284	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0006673	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0000158	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0001324	OMIM:616827	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616827	Muscular dystrophy, limb-girdle, type 2W		HP:0001644	PMID:25589244	PCS					P	HPO:probinson[2017-06-17]
OMIM:600089	Pancreatic beta cell agenesis with neonatal diabetes mellitus		HP:0001438	OMIM:600089	IEA					P	HPO:iea[2009-02-17]
OMIM:600089	Pancreatic beta cell agenesis with neonatal diabetes mellitus		HP:0000007	OMIM:600089	IEA					I	HPO:iea[2009-02-17]
OMIM:600089	Pancreatic beta cell agenesis with neonatal diabetes mellitus		HP:0000857	OMIM:600089	IEA					P	HPO:iea[2009-02-17]
OMIM:609913	Retinitis pigmentosa 32		HP:0000550	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0007737	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0000662	PMID:30157172	PCS	HP:0003621				P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0000580	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0030609	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0000613	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0000007	PMID:30157172	PCS					I	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0000546	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0007663	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0000543	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:609913	Retinitis pigmentosa 32		HP:0007843	PMID:30157172	PCS					P	HPO:probinson[2020-08-31]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0001332	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0001250	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0001252	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0001263	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0005484	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0002490	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0000007	PMID:34954817	PCS					I	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0012444	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0007359	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0032867	PMID:34954817	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620359	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 7		HP:0003623	PMID:34954817	PCS		1/1			C	HPO:probinson[2023-06-14]
OMIM:616833	Paget disease of bone 6		HP:0000121	OMIM:616833	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616833	Paget disease of bone 6		HP:0002653	OMIM:616833	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616833	Paget disease of bone 6		HP:0003155	OMIM:616833	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616833	Paget disease of bone 6		HP:0003581	OMIM:616833	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616833	Paget disease of bone 6		HP:0001712	OMIM:616833	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616833	Paget disease of bone 6		HP:0002757	PMID:26849110	PCS					P	HPO:probinson[2017-06-17]
OMIM:616833	Paget disease of bone 6		HP:0002758	PMID:26849110	PCS					P	HPO:probinson[2017-06-17]
OMIM:616833	Paget disease of bone 6		HP:0000006	PMID:26849110	PCS					I	HPO:probinson[2017-06-17]
OMIM:616833	Paget disease of bone 6		HP:0001677	OMIM:616833	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613793	Blood group, cromer system		HP:0002243	OMIM:613793	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:613793	Blood group, cromer system		HP:0000007	OMIM:613793	IEA					I	HPO:skoehler[2019-04-18]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0001265	PMID:25927242	PCS		2/2			P	HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0003577	PMID:11017805	PCS					C	HPO:probinson[2022-03-16]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0000133	PMID:11017805	PCS		1/1			P	HPO:iea[2010-04-23];HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0006937	PMID:25927242	PCS		2/2			P	HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0000815	PMID:25927242	PCS		2/2			P	HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0001271	PMID:11017805;PMID:25927242	PCS		3/3			P	HPO:iea[2010-04-23];HPO:probinson[2020-12-04];HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0000007	PMID:25927242	PCS					I	HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0003380	PMID:11017805	PCS		1/1			P	HPO:iea[2010-04-23];HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0006886	PMID:25927242	PCS		2/2			P	HPO:probinson[2020-12-04]
OMIM:607080	46XY gonadal dysgenesis with minifascicular neuropathy		HP:0000786	PMID:25927242	PCS	HP:0011462	2/2	FEMALE		P	HPO:probinson[2020-12-04]
OMIM:173200	Pityriasis rubra pilaris		HP:0008392	OMIM:173200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:173200	Pityriasis rubra pilaris		HP:0025474	PMID:22703878	PCS					P	HPO:probinson[2020-08-09]
OMIM:173200	Pityriasis rubra pilaris		HP:0001036	PMID:22703878	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-09]
OMIM:173200	Pityriasis rubra pilaris		HP:0032152	PMID:22703878	PCS					P	HPO:probinson[2020-08-09]
OMIM:173200	Pityriasis rubra pilaris		HP:0025114	PMID:22703878	IEA					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-09]
OMIM:173200	Pityriasis rubra pilaris		HP:0003593	PMID:22703878	PCS					C	HPO:probinson[2020-08-09]
OMIM:173200	Pityriasis rubra pilaris		HP:0000656	OMIM:173200	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:173200	Pityriasis rubra pilaris		HP:0040162	PMID:22703878	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-09]
OMIM:173200	Pityriasis rubra pilaris		HP:0000982	PMID:22703878	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:173200	Pityriasis rubra pilaris		HP:0000006	PMID:22703878	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0008936	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0002015	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0001344	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0002144	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0004322	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0031936	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0001332	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0001250	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0002020	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0003593	PMID:36718090	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0034392	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0001508	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0034353	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0000407	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0000007	PMID:36718090	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0002307	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0000256	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0000545	PMID:36718090	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620417	Spastic paraplegia 90B, autosomal recessive		HP:0001249	PMID:36718090	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0003577	PMID:29861107	PCS		1/6			C	HPO:probinson[2023-02-24];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0001297	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0002980	PMID:29861107	PCS		3/12			P	HPO:probinson[2023-02-24];HPO:skoehler[2019-02-15];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000463	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000023	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000122	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0003155	PMID:29861107	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0003097	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0002020	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0005054	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0003194	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0031485	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0001270	PMID:29861107	PCS		3/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000938	PMID:29861107	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0002757	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0002119	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000774	PMID:29861107	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0001643	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000773	PMID:29861107	PCS		2/12			P	HPO:probinson[2023-02-24];HPO:skoehler[2019-02-15];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000138	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0003026	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0006934	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0001561	PMID:29861107	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0001344	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000750	PMID:29861107	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0030423	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000431	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0011968	PMID:29861107	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0002098	PMID:29861107	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0010537	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0005280	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0034197	PMID:29861107	PCS		5/6			C	HPO:probinson[2023-02-24];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0041159	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0010561	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0001537	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000007	PMID:29861107	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000348	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000843	PMID:29861107	PCS		6/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0002007	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0001334	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000883	PMID:29861107	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000248	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000105	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:618188	Hyperparathyroidism, transient neonatal		HP:0000369	PMID:29861107	PCS		1/6			P	HPO:probinson[2023-02-24]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0001562	PMID:18179883	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0010959	PMID:18179883	PCS		1/3			P	HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0000175	PMID:18179883	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0002089	PMID:18179883	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0030674	PMID:18179883	PCS		3/3			C	HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0005343	PMID:18179883	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0410030	PMID:18179883	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0011743	PMID:18179883	PCS		1/2			P	HPO:iea[2012-07-22];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0012861	PMID:18179883	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0012245	PMID:18179883	PCS		3/3			P	HPO:probinson[2013-04-02];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0001629	PMID:18179883	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0000007	PMID:18179883	PCS					I	HPO:iea[2010-05-11];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0001511	PMID:18179883	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0000047	PMID:18179883	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0005944	OMIM:611812	PCS		HP:0040281			P	HPO:iea[2010-05-11]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0000776	PMID:18179883	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0000369	PMID:18179883	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0004415	PMID:18179883	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:611812	46,XX sex reversal with dysgenesis of kidneys, adrenals, and lungs		HP:0000104	PMID:18179883	PCS		3/3			P	HPO:iea[2010-05-11];HPO:probinson[2023-04-04]
OMIM:309500	Renpenning syndrome		HP:0000286	PMID:15782410	PCS		4/12			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0001572	PMID:15782410	PCS		1/9			P	HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0002023	PMID:15782410	PCS		3/49			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000365	PMID:15782410	PCS		1/36			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0001696	PMID:15782410	PCS	HP:0030674	1/49			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000486	PMID:15782410	PCS		3/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000089	OMIM:309500	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:309500	Renpenning syndrome		HP:0004322	PMID:15782410	PCS		21/36			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0001250	PMID:15782410	PCS		5/44			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000160	PMID:15782410	PCS		3/30			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000518	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0008734	PMID:15782410	PCS		10/28	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0001249	PMID:15782410	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000175	PMID:15782410	PCS		5/49			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000252	PMID:15782410	PCS		38/44			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0002033	OMIM:309500	TAS	HP:0003593				P	HPO:skoehler[2013-06-11]
OMIM:309500	Renpenning syndrome		HP:0001263	PMID:15782410	PCS		52/55			P	HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0012385	OMIM:309500	TAS					P	HPO:skoehler[2013-10-22]
OMIM:309500	Renpenning syndrome		HP:0001419	PMID:15782410	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000767	PMID:15782410	PCS		1/15			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000568	OMIM:309500	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:309500	Renpenning syndrome		HP:0004209	PMID:15782410	PCS		2/22			P	HPO:probinson[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000400	PMID:15782410	PCS		4/30			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000047	PMID:15782410	PCS		2/24			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000322	PMID:15782410	PCS		14/20			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0001257	PMID:15782410	PCS		13/33			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000248	PMID:15782410	PCS		8/18			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000325	OMIM:309500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309500	Renpenning syndrome		HP:0001611	OMIM:309500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309500	Renpenning syndrome		HP:0005338	OMIM:309500	TAS					P	HPO:skoehler[2013-06-02]
OMIM:309500	Renpenning syndrome		HP:0000582	PMID:15782410	PCS		14/31			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000540	OMIM:309500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309500	Renpenning syndrome		HP:0008070	OMIM:309500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309500	Renpenning syndrome		HP:0001629	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0000739	OMIM:309500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309500	Renpenning syndrome		HP:0000618	PMID:15782410	PCS		2/50			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0009640	OMIM:309500	TAS					P	HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000414	OMIM:309500	IEA		5/34			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000219	OMIM:309500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309500	Renpenning syndrome		HP:0000218	PMID:15782410	PCS		7/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0009765	PMID:15782410	PCS		6/27			P	HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000378	PMID:15782410	PCS		13/23			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0001786	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0000411	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0001741	OMIM:309500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309500	Renpenning syndrome		HP:0001347	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0000275	OMIM:309500	TAS	HP:0003621	19/32			P	HPO:probinson[2012-05-01];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0002059	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0002650	OMIM:309500	PCS					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0000431	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0002299	PMID:15782410	PCS		2/22			P	HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000276	OMIM:309500	TAS					P	HPO:probinson[2012-05-01]
OMIM:309500	Renpenning syndrome		HP:0001761	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0000272	PMID:15782410	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0003819	PMID:15782410	PCS		4/52			C	HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0009473	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0000506	PMID:15782410	PCS		2/14			P	HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0001636	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0001631	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:309500	Renpenning syndrome		HP:0000589	PMID:15782410	PCS		2/49			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000303	PMID:15782410	PCS		9/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:309500	Renpenning syndrome		HP:0000347	OMIM:309500	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0001045	OMIM:184850	IEA					P	HPO:skoehler[2010-06-20]
OMIM:184850	Stiff-Person syndrome		HP:0002179	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0002267	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0002960	OMIM:184850	TAS					P	HPO:probinson[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0002063	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0003581	OMIM:184850	IEA					C	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0000819	OMIM:184850	IEA					P	HPO:skoehler[2018-10-08]
OMIM:184850	Stiff-Person syndrome		HP:0000716	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0001903	OMIM:184850	IEA					P	HPO:skoehler[2010-06-20]
OMIM:184850	Stiff-Person syndrome		HP:0007066	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0000739	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0002938	OMIM:184850	IEA					P	HPO:skoehler[2010-06-20]
OMIM:184850	Stiff-Person syndrome		HP:0000756	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0000822	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0007156	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0000975	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0003739	OMIM:184850	TAS					P	HPO:probinson[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0001649	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0001945	OMIM:184850	TAS					P	HPO:skoehler[2012-10-17]
OMIM:184850	Stiff-Person syndrome		HP:0003745	OMIM:184850	IEA					I	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0002359	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0001347	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:184850	Stiff-Person syndrome		HP:0006921	OMIM:184850	IEA					P	HPO:iea[2009-02-17]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0004325	PMID:36996813	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002421	PMID:36996813	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002069	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0010804	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002540	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0004322	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001332	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001250	PMID:36996813	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001252	PMID:36996813	PCS		9/9			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002181	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0033725	PMID:36996813	PCS		9/12			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0007082	PMID:36996813	PCS		13/13			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000639	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000319	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000238	PMID:36996813	PCS		10/12			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002779	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0025336	PMID:36996813	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000631	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000476	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000358	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001765	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0003623	PMID:36996813	PCS		6/13			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002553	PMID:36996813	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001342	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0007109	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000252	PMID:36996813	PCS		4/11			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0007902	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0030423	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000573	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000293	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0011968	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0011400	PMID:36996813	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0005180	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0034197	PMID:36996813	PCS		2/13			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0034198	PMID:36996813	PCS		2/13			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002509	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000646	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000767	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000007	PMID:36996813	PCS					I	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000527	PMID:36996813	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0007359	PMID:36996813	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001257	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001733	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000325	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001655	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000341	PMID:36996813	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000582	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002521	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000541	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000189	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002089	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000463	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0030674	PMID:36996813	PCS		3/13			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0035006	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0100750	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0012447	PMID:36996813	PCS		0/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0006094	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000414	PMID:36996813	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0006970	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000612	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000337	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001789	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0030283	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000218	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0004935	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002514	PMID:36996813	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001347	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0007229	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002135	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0006956	PMID:36996813	PCS		13/13			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000750	PMID:36996813	PCS		9/9			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000431	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001762	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000232	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0030048	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001640	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002132	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001285	PMID:36996813	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002171	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0011344	PMID:36996813	PCS		9/9			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002170	PMID:36996813	PCS		10/10			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002093	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0007371	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0007052	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0034295	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000308	PMID:36996813	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0001518	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000506	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000664	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000303	PMID:36996813	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002324	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0000028	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620371	Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity		HP:0002126	PMID:36996813	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:177700	Glaucoma 1, open angle, P		HP:0003581	PMID:21447600	PCS					C	HPO:probinson[2014-05-24];HPO:probinson[2022-12-22]
OMIM:177700	Glaucoma 1, open angle, P		HP:0012108	PMID:21447600	PCS					P	HPO:probinson[2022-12-22]
OMIM:177700	Glaucoma 1, open angle, P		HP:0012796	PMID:21447600	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2022-12-22]
OMIM:177700	Glaucoma 1, open angle, P		HP:0007854	PMID:21447600	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:177700	Glaucoma 1, open angle, P		HP:0000006	PMID:21447600	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:613977	Cyanosis, transient neonatal		HP:0003577	PMID:19065339	PCS		2/2			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-10]
OMIM:613977	Cyanosis, transient neonatal		HP:0001903	OMIM:613977	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613977	Cyanosis, transient neonatal		HP:0002240	OMIM:613977	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613977	Cyanosis, transient neonatal		HP:0012119	PMID:19065339	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-10]
OMIM:613977	Cyanosis, transient neonatal		HP:0001923	OMIM:613977	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613977	Cyanosis, transient neonatal		HP:0000961	PMID:19065339	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-10]
OMIM:613977	Cyanosis, transient neonatal		HP:0000006	PMID:19065339	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-10]
OMIM:613977	Cyanosis, transient neonatal		HP:0000952	OMIM:613977	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:209500	Atrichia with papular lesions		HP:0007482	OMIM:209500	IEA					P	HPO:iea[2009-02-17]
OMIM:209500	Atrichia with papular lesions		HP:0000007	OMIM:209500	IEA					I	HPO:iea[2009-02-17]
OMIM:209500	Atrichia with papular lesions		HP:0008070	OMIM:209500	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0002257	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0001696	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0002110	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0003251	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0000481	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0100582	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0002090	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0011109	PMID:10577904	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0100750	PMID:10577904	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0012265	PMID:10577904	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0012256	PMID:10577904	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0012263	PMID:10577904	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0001746	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0002837	PMID:10577904	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0000007	PMID:10577904	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0000458	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0000405	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0002315	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0000389	PMID:10577904	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-21]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0001334	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:244400	Ciliary dyskinesia, primary, 1		HP:0002688	OMIM:244400	IEA					P	HPO:iea[2009-02-17]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0001562	PMID:30770808	IEA	HP:0011461	1/4			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0002870	PMID:30770808	PCS		3/3			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0004322	PMID:30770808	PCS		1/3			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0001284	PMID:30770808	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0001270	PMID:30770808	PCS		4/4			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0000007	PMID:30770808	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0001319	PMID:30770808	PCS		4/4			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0001308	PMID:30770808	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0001522	PMID:30770808	PCS		1/4			C	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0002304	PMID:30770808	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0000028	PMID:30770808	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0001513	PMID:30770808	PCS		1/3			P	HPO:probinson[2020-06-27]
OMIM:618822	Myopathy, congenital, with respiratory insufficiency and bone fractures		HP:0003458	PMID:30770808	PCS					P	HPO:probinson[2020-06-27]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0003596	PMID:27510903	PCS		1/5			C	HPO:probinson[2023-07-19];HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0006739	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0002097	PMID:27510903	PCS		2/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0100651	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0001409	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0001903	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0011462	PMID:27510903	PCS		4/5			C	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0000938	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0001888	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0002216	PMID:27510903	PCS		3/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0008404	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0002206	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0001873	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0000006	PMID:27510903	PCS					I	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0002863	PMID:27510903	PCS		1/5			P	HPO:probinson[2023-07-19]
OMIM:620365	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7		HP:0000028	PMID:27510903	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001298	PMID:23910460	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0002344	PMID:23910460	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0005974	OMIM:615453	TAS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001993	PMID:23910460	PCS		2/2		HP:0025303	P	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0002013	PMID:23910460	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0011924	PMID:23910460	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0002151	PMID:23910460	PCS		2/2			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0003593	PMID:23910460	PCS		2/2			C	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0003074	PMID:23910460	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0032653	PMID:23910460	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0002919	PMID:23910460	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001508	PMID:23910460	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0000508	PMID:23910460	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001944	PMID:23910460	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0000007	PMID:23910460	PCS					I	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001987	PMID:23910460	PCS		2/2		HP:0025303	P	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001943	PMID:23910460	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0006554	PMID:23910460	PCS		1/2		HP:0025303	P	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0005979	PMID:23910460	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0002910	PMID:23910460	PCS		2/2		HP:0025303	P	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001510	PMID:23910460	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0001259	PMID:23910460	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:615453	Mitochondrial complex III deficiency, nuclear type 6		HP:0003128	PMID:23910460	PCS		2/2		HP:0025303	P	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-08]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0003593	PMID:32101163	PCS					C	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0100651	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0012594	PMID:32101163	PCS		1/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0010230	PMID:32101163	PCS		3/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000938	PMID:32101163	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0003508	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000696	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000278	PMID:32101163	PCS		1/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0009803	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0002650	PMID:32101163	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0002099	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0030866	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0006480	PMID:32101163	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000826	PMID:32101163	PCS		1/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000704	PMID:32101163	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000407	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000926	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000426	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000007	PMID:32101163	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000703	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000989	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0004209	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000488	PMID:32101163	PCS		2/4		HP:0012825	P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0001510	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0001513	PMID:32101163	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0001831	PMID:32101163	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619269	Ondontochondrodysplasia 2 with hearing loss and diabetes		HP:0000126	PMID:32101163	PCS		1/4			P	HPO:probinson[2021-06-20]
OMIM:618177	Nephrotic syndrome, type 18		HP:0003774	PMID:30179222	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-02]
OMIM:618177	Nephrotic syndrome, type 18		HP:0003676	PMID:30179222	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-02]
OMIM:618177	Nephrotic syndrome, type 18		HP:0003621	PMID:30179222	PCS		2/3			C	HPO:probinson[2021-04-02]
OMIM:618177	Nephrotic syndrome, type 18		HP:0011463	PMID:30179222	PCS		1/3			C	HPO:probinson[2021-04-02]
OMIM:618177	Nephrotic syndrome, type 18		HP:0000097	PMID:30179222	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-02]
OMIM:618177	Nephrotic syndrome, type 18		HP:0000007	PMID:30179222	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-02]
OMIM:618177	Nephrotic syndrome, type 18		HP:0000093	PMID:30179222	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-04-02]
OMIM:618177	Nephrotic syndrome, type 18		HP:0012588	PMID:30179222	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-04-02]
OMIM:617244	Fanconi anemia, complementation group R		HP:0003577	PMID:26253028	PCS		1/1			C	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0000252	PMID:26253028;PMID:26681308	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0003764	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0002023	PMID:26681308	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617244	Fanconi anemia, complementation group R		HP:0002650	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0002144	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0031936	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0003221	PMID:26253028;PMID:26681308	PCS		2/2			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0001903	PMID:26681308	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0007099	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0000238	PMID:26681308	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617244	Fanconi anemia, complementation group R		HP:0000568	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0009777	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0006433	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0005528	PMID:26681308	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0000125	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0001510	PMID:26681308	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617244	Fanconi anemia, complementation group R		HP:0000006	PMID:26681308	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0001249	PMID:26681308	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-10]
OMIM:617244	Fanconi anemia, complementation group R		HP:0006349	PMID:26253028	PCS		1/1			P	HPO:probinson[2023-05-10]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0003621	OMIM:607731	IEA					C	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0003376	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0001761	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0003693	OMIM:607731	TAS					P	HPO:probinson[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0002460	OMIM:607731	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0003450	OMIM:607731	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0003380	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0007083	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0007350	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0009027	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0000007	OMIM:607731	IEA					I	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0002936	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:607731	Charcot-Marie-Tooth disease, axonal, type 2H		HP:0003438	OMIM:607731	IEA					P	HPO:iea[2009-02-17]
OMIM:206800	Anonychia congenita		HP:0001507	PMID:17186469	PCS		0/4			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:206800	Anonychia congenita		HP:0000007	PMID:17186469	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:206800	Anonychia congenita		HP:0001798	PMID:17186469	PCS	HP:0003577	4/4			P	HPO:probinson[2012-07-16];HPO:probinson[2024-03-08]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000341	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0003577	OMIM:613744	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0002540	PMID:20972249	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0004322	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001272	PMID:20972249	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0002120	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001371	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001250	PMID:20972249;PMID:21620353	PCS		3/10			P	HPO:probinson[2023-01-30];HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0003199	OMIM:613744	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001252	PMID:20972249	PCS	HP:0003593	2/2			P	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000280	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0010864	PMID:20972249;PMID:21620353	PCS		10/10			P	HPO:probinson[2023-01-30];HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0100962	PMID:21620353	PCS		5/8			P	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000639	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0011463	PMID:21620353	PCS		3/8			C	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000414	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0002119	PMID:20972249	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001347	PMID:20972249;PMID:21620353	PCS		7/7			P	HPO:probinson[2023-01-30];HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0003623	PMID:21620353	PCS		5/8			C	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000297	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000275	OMIM:613744	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000154	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000494	OMIM:613744	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000252	PMID:20972249;PMID:21620353	PCS		7/10			P	HPO:probinson[2023-01-30];HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000395	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0002510	PMID:20972249	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0003189	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001762	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000431	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0003487	PMID:20972249;PMID:21620353	PCS		4/5			P	HPO:probinson[2023-01-30];HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0031936	PMID:21620353	PCS		6/8			P	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001263	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000646	PMID:21620353	PCS		1/8			P	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000007	PMID:20972249	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001319	OMIM:613744	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001319	PMID:21620353	PCS	HP:0003623	7/7			P	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000307	OMIM:613744	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0025502	PMID:21620353	PCS		2/8			P	HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0002307	PMID:20972249;PMID:21620353	PCS		6/10			P	HPO:probinson[2023-01-30];HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001258	OMIM:613744	TAS					P	HPO:skoehler[2015-01-21]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0000322	OMIM:613744	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613744	Spastic paraplegia 51, autosomal recessive		HP:0001257	PMID:21620353	PCS		7/8			P	HPO:probinson[2023-01-30]
OMIM:231060	Genitopalatocardiac syndrome		HP:0000175	OMIM:231060	TAS					P	HPO:skoehler[2012-07-26]
OMIM:231060	Genitopalatocardiac syndrome		HP:0001629	OMIM:231060	IEA					P	HPO:iea[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0001719	OMIM:231060	TAS					P	HPO:skoehler[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0012020	OMIM:231060	TAS					P	HPO:probinson[2012-07-27]
OMIM:231060	Genitopalatocardiac syndrome		HP:0000107	OMIM:231060	IEA					P	HPO:iea[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0001669	OMIM:231060	IEA					P	HPO:iea[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0000007	OMIM:231060	IEA					I	HPO:iea[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0008668	OMIM:231060	IEA					P	HPO:iea[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0000047	OMIM:231060	IEA					P	HPO:iea[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0000204	OMIM:231060	TAS					P	HPO:skoehler[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0000347	OMIM:231060	IEA					P	HPO:iea[2009-02-17]
OMIM:231060	Genitopalatocardiac syndrome		HP:0000369	OMIM:231060	IEA					P	HPO:iea[2009-02-17]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0001000	PMID:21205863	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0030413	PMID:21205863	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0000007	PMID:21205863	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0005528	PMID:21205863	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0008404	PMID:21205863	PCS		2/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-03-26]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0002745	PMID:21205863	PCS		2/2			P	HPO:probinson[2022-03-26]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0031413	PMID:21205863	PCS		2/2			P	HPO:probinson[2022-03-26]
OMIM:613988	Dyskeratosis congenita, autosomal recessive, 3		HP:0001876	PMID:21205863	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613750	Retinitis pigmentosa 27		HP:0001133	PMID:10192380	PCS		2/5			P	HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0000550	PMID:10192380	PCS		2/5			P	HPO:probinson[2013-08-10];HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0007737	PMID:10192380	PCS		2/5			P	HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0003596	PMID:10192380	PCS		2/3			C	HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0000662	PMID:10192380	PCS		2/5			P	HPO:probinson[2013-08-10];HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0040049	OMIM:613750	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:613750	Retinitis pigmentosa 27		HP:0011462	PMID:10192380	PCS		1/3			C	HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0000618	OMIM:613750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613750	Retinitis pigmentosa 27		HP:0003829	PMID:10192380	PCS					I	HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0007663	PMID:10192380	PCS		2/5			P	HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0007950	OMIM:613750	TAS				HP:0003676	P	HPO:skoehler[2013-08-18]
OMIM:613750	Retinitis pigmentosa 27		HP:0000505	OMIM:613750	TAS					P	HPO:probinson[2013-08-10]
OMIM:613750	Retinitis pigmentosa 27		HP:0007401	OMIM:613750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613750	Retinitis pigmentosa 27		HP:0000510	PMID:10192380	PCS		3/5			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0007843	PMID:10192380	PCS		1/5			P	HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0000006	PMID:10192380	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-04-07]
OMIM:613750	Retinitis pigmentosa 27		HP:0000533	OMIM:613750	TAS					P	HPO:probinson[2013-08-10]
OMIM:603543	Limb-Mammary syndrome		HP:0000175	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0002164	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0000193	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0001171	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0012385	OMIM:603543	TAS					P	HPO:skoehler[2013-10-22]
OMIM:603543	Limb-Mammary syndrome		HP:0009473	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0001839	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0000668	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0001822	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0000966	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0001159	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0002557	OMIM:603543	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603543	Limb-Mammary syndrome		HP:0000564	OMIM:603543	IEA					P	HPO:iea[2009-02-17]
OMIM:603543	Limb-Mammary syndrome		HP:0000006	OMIM:603543	IEA					I	HPO:iea[2009-02-17]
OMIM:194470	Zinc, elevated plasma		HP:0001939	OMIM:194470	IEA					P	HPO:iea[2009-02-17]
OMIM:194470	Zinc, elevated plasma		HP:0000006	OMIM:194470	IEA					I	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000486	PMID:15884042	PCS		17/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000244	OMIM:182212	IEA					P	HPO:skoehler[2019-02-22]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001252	PMID:15884042	PCS		26/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0002020	PMID:15884042	PCS		4/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001290	OMIM:182212	IEA					P	HPO:skoehler[2018-10-08]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0009023	PMID:15884042	PCS		5/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0002816	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0011220	PMID:15884042	PCS		17/37			P	HPO:iea[2018-03-13]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000316	OMIM:182212	PCS		28/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000238	PMID:15884042	PCS		13/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0002857	PMID:15884042	PCS		4/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0003745	OMIM:182212	IEA					I	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001840	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001763	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001249	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000358	PMID:15884042	PCS		32/37			P	HPO:probinson[2023-02-11]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000494	OMIM:182212	PCS		31/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000252	PMID:15884042	PCS		6/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0002870	OMIM:182212	PCS		6/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001382	PMID:15884042;OMIM:182212	PCS		31/47			P	HPO:iea[2018-03-13];HPO:skoehler[2018-10-08]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001263	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0003083	PMID:15884042	PCS		5/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0012385	PMID:15884042	PCS		24/37			P	HPO:skoehler[2013-10-22]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0008440	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000327	PMID:15884042	PCS		16/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000767	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001537	PMID:15884042	PCS		13/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000689	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0003717	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000405	PMID:15884042	PCS		5/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000768	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0005815	OMIM:182212	PCS		5/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000520	PMID:15884042	PCS		29/37			P	HPO:iea[2018-03-13]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000883	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000006	OMIM:182212	TAS					I	HPO:skoehler[2013-01-21]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000369	PMID:15884042	PCS		32/37			P	HPO:probinson[2023-02-11]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0003016	OMIM:182212	PCS		4/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000189	OMIM:182212	TAS					P	HPO:skoehler[2013-08-18]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000023	OMIM:182212	IEA		19/34			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000463	PMID:15884042	PCS		9/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000260	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000938	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0008872	OMIM:182212	PCS		9/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000218	PMID:15884042	PCS		30/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000895	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000377	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000974	OMIM:182212	PCS		7/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001166	PMID:15884042	PCS		34/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001363	PMID:15884042	PCS		18/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0002650	OMIM:182212	PCS		23/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001762	OMIM:182212	PCS		13/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0009473	PMID:15884042	PCS		7/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000506	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0007099	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000508	PMID:15884042	PCS		16/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000268	PMID:15884042	PCS		28/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0002007	OMIM:182212	IEA					P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000586	PMID:15884042	PCS		13/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000028	OMIM:182212	PCS		1/13	MALE		P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000347	PMID:15884042	PCS		33/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0001634	PMID:15884042	PCS		13/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0000545	PMID:15884042	PCS		9/37			P	HPO:iea[2009-02-17]
OMIM:182212	Shprintzen-Goldberg craniosynostosis syndrome		HP:0004942	PMID:15884042	PCS		8/37			P	HPO:iea[2009-02-17]
OMIM:611147	Paroxysmal nonkinesigenic dyskinesia 2		HP:0002268	OMIM:611147	TAS					P	HPO:probinson[2009-02-17]
OMIM:611147	Paroxysmal nonkinesigenic dyskinesia 2		HP:0001250	OMIM:611147	IEA					P	HPO:iea[2009-02-17]
OMIM:611147	Paroxysmal nonkinesigenic dyskinesia 2		HP:0002076	OMIM:611147	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:611147	Paroxysmal nonkinesigenic dyskinesia 2		HP:0003829	OMIM:611147	IEA					I	HPO:iea[2009-02-17]
OMIM:611147	Paroxysmal nonkinesigenic dyskinesia 2		HP:0000006	OMIM:611147	IEA					I	HPO:iea[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0001012	OMIM:145981	TAS					P	HPO:iea[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0004398	OMIM:145981	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0002918	PMID:23802516	PCS		10/10			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0008200	OMIM:145981	IEA					P	HPO:skoehler[2010-06-20]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0003529	OMIM:145981	TAS					P	HPO:iea[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0000934	OMIM:145981	TAS					P	HPO:iea[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0003072	OMIM:145981	TAS					P	HPO:iea[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0000787	OMIM:145981	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0001733	OMIM:145981	TAS					P	HPO:iea[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0003127	OMIM:145981	TAS					P	HPO:iea[2009-02-17]
OMIM:145981	Hypocalciuric hypercalcemia, familial, type II		HP:0000006	OMIM:145981;PMID:23802516	PCS		20/20			I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HP:probinson[2019-03-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0001166	PMID:25434006	PCS		2/6			P	HPO:skoehler[2015-03-22];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0012727	PMID:25434006	PCS					P	HPO:skoehler[2015-03-22];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0003581	PMID:25434006	PCS		8/8			C	HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0005110	PMID:25434006	PCS		2/8			P	HPO:skoehler[2015-03-22];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0100775	PMID:25434006	PCS		3/4			P	HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0001519	PMID:25434006	PCS					P	HPO:probinson[2021-05-01];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0000767	PMID:25434006	PCS		2/8			P	HPO:skoehler[2015-03-22];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0000768	PMID:25434006	PCS		1/8			P	HPO:skoehler[2015-03-22];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0000218	PMID:25434006	PCS		2/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0006687	PMID:25434006	PCS		2/5			P	HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0004933	PMID:25434006	PCS		1/8			P	HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0001634	PMID:25434006	PCS		1/8			P	HPO:skoehler[2015-03-22];HPO:probinson[2021-05-01]
OMIM:616166	Aortic aneurysm, familial thoracic 9		HP:0000006	PMID:25434006	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-01]
OMIM:619255	Baralle-Macken syndrome		HP:0000582	PMID:33632302	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0002540	PMID:33632302	PCS		4/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001332	PMID:33632302	PCS		1/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0000020	PMID:33632302	PCS		2/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0002283	PMID:33632302	PCS		1/6		HP:0012825	P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0003593	PMID:33632302	PCS		6/6			C	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0000518	PMID:33632302	PCS		6/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0000957	PMID:33632302	PCS		1/6			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0000956	PMID:33632302	PCS		2/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001763	PMID:33632302	PCS		1/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001007	PMID:33632302	PCS		2/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0000252	PMID:33632302	PCS		5/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001344	PMID:33632302	PCS		2/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0000750	PMID:33632302	PCS		5/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0031936	PMID:33632302	PCS		6/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0002076	PMID:33632302	PCS		1/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001065	PMID:33632302	PCS		2/6			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001182	PMID:33632302	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0002808	PMID:33632302	PCS		2/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0000007	PMID:33632302	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0002705	PMID:33632302	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001319	PMID:33632302	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0007359	PMID:33632302	PCS		1/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001257	PMID:33632302	PCS		4/6			P	HPO:probinson[2021-06-20]
OMIM:619255	Baralle-Macken syndrome		HP:0001513	PMID:33632302	PCS		2/6			P	HPO:probinson[2021-06-20]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003697	OMIM:608358	IEA					P	HPO:iea[2009-02-17]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003198	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003551	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003691	PMID:14520662	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage		HP:0011463	PMID:14520662	PCS		3/3			C	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003707	PMID:14520662	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0009046	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003749	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0002515	PMID:14520662	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003803	OMIM:608358	IEA					P	HPO:iea[2009-02-17]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003704	OMIM:608358	IEA					P	HPO:iea[2009-02-17]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003547	PMID:14520662	PCS		4/4			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0001324	PMID:14520662	PCS		2/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003724	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003722	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003324	OMIM:608358	IEA					P	HPO:iea[2009-02-17]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003687	OMIM:608358	IEA					P	HPO:iea[2009-02-17]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0001288	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0002792	PMID:14520662	PCS		1/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0008180	PMID:14520662	PCS		2/4			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0001639	PMID:14520662	PCS		0/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0009055	OMIM:608358	IEA					P	HPO:iea[2009-02-17]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0002527	PMID:14520662	PCS		1/4			P	HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003677	OMIM:608358	IEA					C	HPO:iea[2009-02-17]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0000006	PMID:14520662	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:608358	Myopathy, myosin storage, autosomal dominant		HP:0003458	PMID:14520662	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:425500	HAIRY EARS, Y-LINKED		HP:0000598	OMIM:425500	IEA					P	HPO:iea[2009-02-17]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0003202	OMIM:612300	TAS				HP:0003676	P	HPO:skoehler[2013-09-30]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0001271	OMIM:612300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0001252	OMIM:612300	TAS					P	HPO:skoehler[2014-11-26]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0004818	PMID:1699124	PCS					P	HPO:probinson[2013-01-09]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0001284	OMIM:612300	TAS					P	HPO:skoehler[2013-09-30]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0003593	OMIM:612300	TAS					C	HPO:skoehler[2015-12-30]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0001878	OMIM:612300	TAS					P	HPO:skoehler[2013-09-30]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0001290	OMIM:612300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0000007	PMID:1382994	PCS					I	HPO:probinson[2013-04-06]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0003690	OMIM:612300	TAS					P	HPO:skoehler[2013-09-30]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0003470	OMIM:612300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612300	Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy		HP:0002922	OMIM:612300	TAS					P	HPO:skoehler[2013-09-30]
OMIM:191520	Upington disease		HP:0006429	OMIM:191520	IEA					P	HPO:iea[2009-02-17]
OMIM:191520	Upington disease		HP:0003365	OMIM:191520	TAS					P	HPO:probinson[2013-08-10]
OMIM:191520	Upington disease		HP:0002829	OMIM:191520	IEA					P	HPO:iea[2009-02-17]
OMIM:191520	Upington disease		HP:0000006	OMIM:191520	IEA					I	HPO:iea[2009-02-17]
OMIM:191520	Upington disease		HP:0008812	OMIM:191520	IEA					P	HPO:iea[2009-02-17]
OMIM:191520	Upington disease		HP:0005701	OMIM:191520	TAS					P	HPO:probinson[2013-08-10]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0002257	PMID:21496787	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0012265	PMID:21496787	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0001696	PMID:21496787	PCS	HP:0003577	3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0012256	PMID:21496787	PCS		3/3			P	HPO:probinson[2013-04-07];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0002110	PMID:21496787	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0012262	PMID:21496787	PCS		3/3			P	HPO:probinson[2013-04-07];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0000007	PMID:21496787	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0010444	PMID:21496787	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0000389	PMID:21496787	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0011109	PMID:21496787	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-09]
OMIM:614017	Ciliary dyskinesia, primary, 16		HP:0003623	PMID:21496787	PCS		3/3			C	HPO:probinson[2021-10-09]
OMIM:301835	Arts syndrome		HP:0000572	OMIM:301835	IEA					P	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0003323	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0002015	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0000365	OMIM:301835	IEA					P	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0001344	OMIM:301835	TAS					P	HPO:skoehler[2014-11-26]
OMIM:301835	Arts syndrome		HP:0001250	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0001263	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0001251	OMIM:301835	IEA					P	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0001284	OMIM:301835	IEA					P	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0002719	PMID:8498830	PCS					P	HPO:skoehler[2009-09-17];HP:probinson[2019-01-03]
OMIM:301835	Arts syndrome		HP:0000639	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0001419	OMIM:301835	IEA					I	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0009830	OMIM:301835	TAS				HP:0003676	P	HPO:skoehler[2013-06-06]
OMIM:301835	Arts syndrome		HP:0008311	OMIM:301835	IEA					P	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0000648	OMIM:301835	IEA					P	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0001319	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0002307	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0001522	OMIM:301835	IEA					C	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0002788	OMIM:301835	IEA					P	HPO:iea[2009-02-17]
OMIM:301835	Arts syndrome		HP:0001510	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0002445	OMIM:301835	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301835	Arts syndrome		HP:0001249	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0002721	OMIM:301835	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301835	Arts syndrome		HP:0001347	OMIM:301835	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610265	Deafness, autosomal recessive 67		HP:0003577	PMID:16459341	PCS		13/13			C	HPO:probinson[2024-03-14]
OMIM:610265	Deafness, autosomal recessive 67		HP:0001751	PMID:16459341	PCS		0/13			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-14]
OMIM:610265	Deafness, autosomal recessive 67		HP:0008619	PMID:16752389	PCS	HP:0003593				P	HPO:lccarmody[2018-10-04]
OMIM:610265	Deafness, autosomal recessive 67		HP:0000407	PMID:16459341	PCS	HP:0003577	13/13			P	HPO:probinson[2013-04-01];HPO:probinson[2024-03-14]
OMIM:610265	Deafness, autosomal recessive 67		HP:0001098	PMID:16459341	PCS		0/13			P	HPO:probinson[2024-03-14]
OMIM:610265	Deafness, autosomal recessive 67		HP:0000007	PMID:16459341	PCS					I	HPO:probinson[2013-01-09]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0010804	OMIM:606407	TAS					P	HPO:probinson[2013-08-10]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0010628	OMIM:606407	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0003577	PMID:11524703	PCS		7/7			C	HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001250	PMID:11524703	PCS	HP:0003623	5/7			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001252	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0003131	PMID:11524703	PCS		7/7			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001290	OMIM:606407	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000815	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001508	PMID:11524703	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0008872	PMID:11524703	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0008897	PMID:11524703	PCS		7/7			P	HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001324	OMIM:606407	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001466	OMIM:606407	IEA					I	HPO:skoehler[2012-11-20]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000358	PMID:11524703	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0003128	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0008936	PMID:11524703	PCS	HP:0003577	7/7			P	HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0003200	PMID:11524703	PCS		1/1			P	HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0031936	PMID:11524703	PCS		7/7			P	HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0002591	OMIM:606407	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001263	PMID:11524703	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0002151	PMID:11524703	PCS		4/7			P	HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0005280	PMID:11524703	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0033067	PMID:11524703	PCS		7/7			P	HPO:probinson[2022-09-07];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000508	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001998	OMIM:606407	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001558	PMID:11524703	PCS	HP:0011461	2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000007	PMID:11524703	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001319	OMIM:606407	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000527	PMID:11524703	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000824	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0002901	PMID:11524703	PCS	HP:0003623	4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000400	PMID:11524703	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0002007	PMID:11524703	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000268	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0000787	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001612	PMID:11524703	PCS		7/7			P	HPO:probinson[2022-09-07]
OMIM:606407	Hypotonia-cystinuria syndrome		HP:0001611	OMIM:606407	IEA					P	HPO:iea[2009-02-17]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0001396	OMIM:609734	TAS					P	HPO:probinson[2013-03-30]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0011748	PMID:9620771	PCS		2/2			P	HPO:probinson[2013-03-30];HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0002297	PMID:9620771	PCS		2/2			P	HPO:probinson[2013-03-30];HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0002173	OMIM:609734	TAS					P	HPO:probinson[2013-03-30]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0002591	PMID:9620771	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0003593	PMID:9620771	PCS		1/2			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0033579	PMID:9620771	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0008163	PMID:9620771	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0002904	OMIM:609734	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0008213	OMIM:609734	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0000007	PMID:9620771	PCS					I	HPO:probinson[2013-03-30];HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0000846	OMIM:609734	IEA					P	HPO:skoehler[2015-01-19]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0000835	OMIM:609734	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0000824	OMIM:609734	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0001513	PMID:9620771	PCS		2/2			P	HPO:probinson[2013-01-09];HPO:probinson[2023-03-04]
OMIM:609734	Obesity, early-onset, with adrenal insufficiency and red hair		HP:0003623	PMID:9620771	PCS		1/2			C	HPO:probinson[2023-03-04]
OMIM:274500	Thyroid hormonogenesis, genetic defect in, 2A		HP:0031507	PMID:8027236	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:274500	Thyroid hormonogenesis, genetic defect in, 2A		HP:0008263	PMID:8027236	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-12]
OMIM:274500	Thyroid hormonogenesis, genetic defect in, 2A		HP:0003593	PMID:8027236	PCS		1/1			C	HPO:probinson[2022-06-12]
OMIM:274500	Thyroid hormonogenesis, genetic defect in, 2A		HP:0000007	OMIM:274500	IEA					I	HPO:iea[2009-02-17]
OMIM:274500	Thyroid hormonogenesis, genetic defect in, 2A		HP:0000821	PMID:8027236	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-12]
OMIM:274500	Thyroid hormonogenesis, genetic defect in, 2A		HP:0000853	PMID:8027236	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-12]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0030674	PMID:33257696	PCS		1/8			C	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0001250	PMID:33257696	PCS		7/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002120	PMID:33257696	PCS		7/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0010862	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0033725	PMID:33257696	PCS		8/14			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0012110	PMID:33257696	PCS		1/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000639	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000518	PMID:33257696	PCS		4/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002119	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0003623	PMID:33257696	PCS		7/8			C	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0008936	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0003202	PMID:33257696	PCS		7/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002510	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002015	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000010	PMID:33257696	PCS		1/7			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0001344	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002650	PMID:33257696	PCS		7/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0001321	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002194	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002071	PMID:33257696	PCS		7/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002509	PMID:33257696	PCS		8/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000508	PMID:33257696	PCS		4/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000448	PMID:33257696	PCS		2/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000007	PMID:33257696	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000648	PMID:33257696	PCS		4/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0002104	PMID:33257696	PCS		1/8			P	HPO:probinson[2021-10-23]
OMIM:619527	Pontocerebellar hypoplasia, type 16		HP:0000369	PMID:33257696	PCS		2/8			P	HPO:probinson[2021-10-23]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0002069	PMID:25362483	PCS		10/29			P	HPO:skoehler[2015-02-22]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0003621	PMID:25362483	PCS		1/25			C	HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0000750	PMID:25362483	PCS		2/29			P	HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0002384	PMID:25362483	PCS		4/29			P	HPO:skoehler[2015-02-22]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0002373	PMID:25362483	PCS		20/27			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0002121	PMID:25362483	PCS		5/29			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0010819	PMID:25362483	PCS		3/29			P	HPO:skoehler[2015-02-22]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0011463	PMID:25362483	PCS		22/25			C	HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0001263	OMIM:616172	TAS		5/29			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0032792	PMID:25362483	PCS		8/29			P	HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0003593	PMID:25362483	PCS		2/25			C	HPO:probinson[2023-04-02]
OMIM:616172	Generalized epilepsy with febrile seizures plus, type 9		HP:0000006	PMID:25362483	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-02]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003510	OMIM:609052	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0004699	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003016	OMIM:609052	TAS					P	HPO:probinson[2012-05-26]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0001156	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0002673	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003300	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003025	OMIM:609052	TAS					P	HPO:probinson[2012-05-26]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003375	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0005041	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003180	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003090	OMIM:609052	TAS					P	HPO:probinson[2012-05-26]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0100865	OMIM:609052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0003918	OMIM:609052	TAS					P	HPO:probinson[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0008076	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0000926	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0008873	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0000007	OMIM:609052	IEA					I	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0000920	OMIM:609052	TAS					P	HPO:iea[2012-05-26]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0000768	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0004979	OMIM:609052	TAS					P	HPO:probinson[2012-05-26]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0000268	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0002657	OMIM:609052	TAS					P	HPO:probinson[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0006369	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:609052	Spondylometaphyseal dysplasia, type A4		HP:0006623	OMIM:609052	IEA					P	HPO:iea[2009-02-17]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0003621	PMID:18984066	PCS		1/4			C	HPO:probinson[2022-05-08]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000670	PMID:18984066	PCS		9/46			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0001596	OMIM:612843	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0004552	PMID:18984066	PCS		39/46			P	HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0002164	OMIM:612843	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000491	PMID:18984066	PCS		19/47			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0001041	PMID:18984066	PCS		21/47			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0045075	PMID:18984066	PCS		7/8			P	HPO:probinson[2022-05-08]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0025084	PMID:18984066	PCS		17/47			P	HPO:skoehler[2017-07-13];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0032152	PMID:18984066	PCS		45/47			P	HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000518	PMID:18984066	PCS		3/47			P	HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0011463	PMID:18984066	PCS		3/4			C	HPO:probinson[2022-05-08]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000509	PMID:18984066	PCS		17/47			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0006297	PMID:18984066	PCS		9/46			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000613	PMID:18984066	PCS		26/47			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0030054	OMIM:612843	TAS					P	HPO:skoehler[2014-09-21]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000653	PMID:18984066	PCS		42/47			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0008404	PMID:18984066	PCS		15/46			P	HPO:skoehler[2013-05-03];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000982	PMID:18984066	PCS		8/47			P	HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000498	PMID:18984066	PCS		17/47			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:612843	Keratosis follicularis spinulosa decalvans, autosomal dominant		HP:0000006	PMID:18984066	PCS					I	HPO:skoehler[2010-06-19];HP:probinson[2019-01-26]
OMIM:313000	Spatial visualization, aptitude for		HP:0001419	OMIM:313000	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:313000	Spatial visualization, aptitude for		HP:0000707	OMIM:313000	IEA					P	HPO:iea[2009-02-17]
OMIM:120300	Coloboma of macula		HP:0000006	OMIM:120300	TAS					I	HPO:probinson[2009-02-17]
OMIM:120300	Coloboma of macula		HP:0001116	OMIM:120300	TAS					P	HPO:probinson[2012-07-26]
OMIM:620629	Optic atrophy 16		HP:0000572	PMID:37734847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0003621	PMID:37734847	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0000407	PMID:37734847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0011462	PMID:37734847	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0007641	PMID:37734847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0007663	PMID:37734847	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0000007	PMID:37734847	PCS					I	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0000648	PMID:37734847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0000603	PMID:37734847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0002315	PMID:37734847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620629	Optic atrophy 16		HP:0012511	PMID:37734847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:300068	Androgen insensitivity syndrome		HP:0000066	OMIM:300068	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300068	Androgen insensitivity syndrome		HP:0002664	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0000023	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0000771	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0002550	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0011969	OMIM:300068	TAS					P	HPO:probinson[2015-06-02]
OMIM:300068	Androgen insensitivity syndrome		HP:0040314	OMIM:300068	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300068	Androgen insensitivity syndrome		HP:0001419	OMIM:300068	IEA					I	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0001507	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0008232	OMIM:300068	TAS					P	HPO:probinson[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0008730	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0002225	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0000786	OMIM:300068	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300068	Androgen insensitivity syndrome		HP:0002215	OMIM:300068	IEA					P	HPO:iea[2009-02-17]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0012264	PMID:27486783	PCS					P	HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0002257	PMID:27486783	PCS		3/3			P	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0002110	PMID:27486783	PCS		3/3			P	HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0003251	PMID:27486783	PCS		1/1	MALE		P	HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0033036	PMID:27486783	PCS		3/3			P	HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0033158	PMID:27486783	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0000007	PMID:27486783	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0002837	PMID:27486783	PCS		2/3			P	HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0012208	PMID:27486783	PCS		1/1	MALE		P	HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0011108	PMID:27486783	PCS		3/3			P	HPO:probinson[2020-09-13]
OMIM:617091	Ciliary dyskinesia, primary, 34		HP:0002643	PMID:27486783	PCS	HP:0003623	1/3			P	HPO:probinson[2020-09-13]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0000750	PMID:31785787	PCS		5/5			P	HPO:probinson[2023-06-04]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0002650	PMID:31785787	PCS		2/5			P	HPO:probinson[2023-06-04]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0001321	PMID:31785787	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0000639	OMIM:213000	IEA					P	HPO:iea[2009-02-17]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0001250	PMID:31785787	PCS		5/5			P	HPO:probinson[2023-06-04]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0001252	PMID:31785787	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0001263	PMID:31785787	PCS		5/5			P	HPO:probinson[2023-06-04]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0001251	OMIM:213000	IEA					P	HPO:iea[2009-02-17]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0000007	PMID:31785787	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0001337	OMIM:213000	IEA					P	HPO:iea[2009-02-17]
OMIM:213000	Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay		HP:0001249	PMID:31785787	PCS		5/5			P	HPO:probinson[2023-06-04]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0003202	PMID:24482476	PCS		1/2			P	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0001276	PMID:24482476	PCS		2/2			P	HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0002169	PMID:24482476	PCS		1/2			P	HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0031936	PMID:24482476	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0001288	PMID:24482476	PCS		2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0002079	PMID:24482476	PCS		1/2			P	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0004322	PMID:24482476	PCS		1/2			P	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0003487	PMID:24482476	PCS		2/2			P	HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0006938	PMID:24482476	PCS		1/2			P	HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0012407	PMID:24482476	PCS		2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0002518	PMID:24482476	PCS		1/1			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0000007	PMID:24482476	PCS					I	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0001258	PMID:24482476	PCS					P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0001249	PMID:24482476	PCS		0/2			P	HPO:probinson[2022-04-11]
OMIM:615686	Spastic paraplegia 63, autosomal recessive		HP:0001347	PMID:24482476	PCS		2/2			P	HPO:skoehler[2015-09-09];HPO:probinson[2022-04-11]
OMIM:164230	Obsessive-Compulsive disorder 1		HP:0012166	PMID:15820710	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:164230	Obsessive-Compulsive disorder 1		HP:0000716	PMID:15820710	PCS					P	HPO:lccarmody[2018-10-02];HPO:lccarmody[2018-10-02]
OMIM:164230	Obsessive-Compulsive disorder 1		HP:0030212	PMID:15820710	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:164230	Obsessive-Compulsive disorder 1		HP:0000739	PMID:15820710	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:164230	Obsessive-Compulsive disorder 1		HP:0000722	OMIM:164230	IEA					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-02];HP:probinson[2019-01-03];HPO:probinson[2022-08-27]
OMIM:164230	Obsessive-Compulsive disorder 1		HP:0000006	OMIM:164230	TAS					I	HPO:skoehler[2013-05-29]
OMIM:217500	Corneal dystrophy, band-shaped		HP:0007709	OMIM:217500	IEA					P	HPO:iea[2009-02-17]
OMIM:217500	Corneal dystrophy, band-shaped		HP:0000007	OMIM:217500	IEA					I	HPO:iea[2009-02-17]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0003621	PMID:35397207	PCS		2/15			C	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0001971	PMID:35397207	PCS		2/15			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0005565	PMID:35397207	PCS		3/14			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0032948	PMID:35397207	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0003593	PMID:35397207	PCS		1/15			C	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0001394	PMID:35397207	PCS		7/15			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0002480	PMID:35397207	PCS		2/15			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0032622	PMID:35397207	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0012852	PMID:35397207	PCS		5/15			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0001409	PMID:35397207	PCS		10/15			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0011463	PMID:35397207	PCS		5/15			C	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0001639	PMID:35397207	PCS	HP:0003581	3/15			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0011462	PMID:35397207	PCS		7/15			C	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0004719	PMID:35397207	PCS		6/14			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0000107	PMID:35397207	PCS		7/14			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0000007	PMID:35397207	PCS					I	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0001433	PMID:35397207	PCS		9/15			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0002910	PMID:35397207	PCS		10/15			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0000952	PMID:35397207	PCS					P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0000105	PMID:35397207	PCS		4/14			P	HPO:probinson[2022-07-19]
OMIM:619902	Hepatorenocardiac degenerative fibrosis		HP:0001402	PMID:35397207	PCS	HP:0011462	1/15			P	HPO:probinson[2022-07-19]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0001792	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2010-07-09]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0003038	OMIM:228900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0008905	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0001772	OMIM:228900	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0001156	PMID:12121354	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0002990	PMID:2363425	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0010049	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0004097	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2010-07-09]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0010624	OMIM:228900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0010743	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0006092	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0010760	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2010-07-09]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0000007	OMIM:228900	PCS					I	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0002999	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2010-07-09]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0009803	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:228900	Fibular hypoplasia and complex brachydactyly		HP:0008119	PMID:12121354	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:620173	Tooth agenesis, selective, 10		HP:0000341	PMID:30046887	PCS		1/4			P	HPO:probinson[2023-03-04]
OMIM:620173	Tooth agenesis, selective, 10		HP:0000252	PMID:30046887	PCS		1/4			P	HPO:probinson[2023-03-04]
OMIM:620173	Tooth agenesis, selective, 10		HP:0000007	PMID:30046887	PCS					I	HPO:probinson[2023-03-04]
OMIM:620173	Tooth agenesis, selective, 10		HP:0000218	PMID:30046887	PCS		1/4			P	HPO:probinson[2023-03-04]
OMIM:620173	Tooth agenesis, selective, 10		HP:0000369	PMID:30046887	PCS		1/4			P	HPO:probinson[2023-03-04]
OMIM:620173	Tooth agenesis, selective, 10		HP:0000677	PMID:30046887	PCS		4/4			P	HPO:probinson[2023-03-04]
OMIM:265800	Pycnodysostosis		HP:0000670	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0003302	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0000189	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0002650	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0001156	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0009839	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0004322	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0004474	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0000680	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0011001	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0001807	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	PYCNODYSOSTOSIS		HP:0006660	OMIM:265800	TAS					P	HPO:probinson[2022-07-01]
OMIM:265800	Pycnodysostosis		HP:0000668	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0000448	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0000007	OMIM:265800	IEA					I	HPO:iea[2009-02-17]
OMIM:265800	PYCNODYSOSTOSIS		HP:0002868	OMIM:265800	TAS					P	HPO:probinson[2022-07-01]
OMIM:265800	Pycnodysostosis		HP:0002007	OMIM:265800	TAS					P	HPO:probinson[2012-05-01]
OMIM:265800	Pycnodysostosis		HP:0006335	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0002645	OMIM:265800	TAS					P	HPO:probinson[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0000696	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0000347	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0002688	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:265800	Pycnodysostosis		HP:0000269	OMIM:265800	TAS					P	HPO:probinson[2012-05-01]
OMIM:265800	Pycnodysostosis		HP:0003304	OMIM:265800	IEA					P	HPO:iea[2009-02-17]
OMIM:617907	Erythrocytosis, familial, 5		HP:0001900	PMID:29514032	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617907	Erythrocytosis, familial, 5		HP:0001899	PMID:29514032	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617907	Erythrocytosis, familial, 5		HP:0033644	PMID:29514032	PCS					P	HPO:probinson[2022-10-01]
OMIM:617907	Erythrocytosis, familial, 5		HP:0001901	PMID:29514032	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617907	Erythrocytosis, familial, 5		HP:0000006	PMID:29514032	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:619094	Spermatogenic failure 45		HP:0032560	PMID:30811583	PCS		4/4			P	HPO:probinson[2020-12-15]
OMIM:619094	Spermatogenic failure 45		HP:0003251	PMID:30811583	PCS		4/4			P	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619094	Spermatogenic failure 45		HP:0000007	PMID:30811583	PCS					I	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619094	Spermatogenic failure 45		HP:0012207	PMID:30811583	PCS		4/4			P	HPO:probinson[2020-12-15]
OMIM:619094	Spermatogenic failure 45		HP:0032558	PMID:30811583	PCS		4/4			P	HPO:probinson[2020-12-15]
OMIM:619094	Spermatogenic failure 45		HP:0032559	PMID:30811583	PCS		4/4			P	HPO:probinson[2020-12-15]
OMIM:601803	Pallister-Killian syndrome		HP:0002025	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0002023	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000365	PMID:25888713;PMID:32714624	PCS		18/24			P	HP:probinson[2021-10-19];HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0002540	PMID:25888713	PCS		4/13			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0002144	PMID:33269168	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0003196	PMID:32714624	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001290	PMID:32714624	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000518	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000639	PMID:25888713	PCS		5/22			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000878	PMID:25888713	PCS		2/8			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0001169	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001601	PMID:32482921	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000358	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001344	PMID:25888713	PCS		14/22			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0005026	PMID:25888713	PCS		5/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0002033	PMID:32482921	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0002827	PMID:25888713	PCS		3/22			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0004209	PMID:25888713	PCS		4/21			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000400	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000520	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000369	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000402	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001612	PMID:32482921	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001215	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001276	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0002883	OMIM:601803	TAS					P	HPO:skoehler[2015-12-30]
OMIM:601803	Pallister-Killian syndrome		HP:0000066	PMID:19215037	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0003577	PMID:32482921;PMID:19215037	PCS		2/2			C	HPO:probinson[2021-10-19];HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0000582	PMID:32714624	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000343	PMID:32714624;PMID:19215037	PCS		3/3			P	HPO:probinson[2022-05-08];HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0002089	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0008905	OMIM:601803	TAS					P	HPO:probinson[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000463	PMID:32714624	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0008070	PMID:33269168;PMID:32714624	PCS		2/3			P	HPO:probinson[2021-10-19];HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0006297	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000219	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0002119	PMID:25888713	PCS		3/14			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000059	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001788	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001545	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000110	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001561	PMID:25888713	PCS	HP:0011461	4/16			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0004279	PMID:25888713	PCS		12/21			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000232	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001442	PMID:25888713	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0001162	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000193	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001680	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0005484	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000470	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000506	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0040288	PMID:32482921	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000629	PMID:19215037	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0000508	PMID:25888713;PMID:19215037	PCS		6/22			P	HPO:probinson[2022-05-08];HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000107	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000348	PMID:33269168	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000505	PMID:25888713	PCS		17/22			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0002007	PMID:32714624	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001830	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0007535	PMID:32714624	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000465	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000347	PMID:32714624	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001831	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001650	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000286	PMID:32714624	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001374	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0010804	PMID:32482921;PMID:32714624	PCS		2/3			P	HPO:probinson[2021-10-19];HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000684	PMID:25888713	PCS		12/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0001773	PMID:25888713;PMID:19215037	PCS		13/22			P	HPO:probinson[2022-05-08];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000046	OMIM:601803	TAS					P	HPO:skoehler[2015-02-22]
OMIM:601803	Pallister-Killian syndrome		HP:0001371	PMID:25888713	PCS		3/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0001250	PMID:25888713;PMID:32482921	PCS		17/23			P	HPO:probinson[2021-10-19];HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0001010	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001252	PMID:25888713;PMID:33269168;PMID:32482921;PMID:19215037	PCS		4/24			P	HPO:probinson[2021-10-19];HPO:probinson[2022-05-08];HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0004482	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000280	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0045075	PMID:32714624;PMID:19215037	PCS		3/3			P	HP:probinson[2021-10-19];HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0012673	OMIM:601803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601803	Pallister-Killian syndrome		HP:0011220	PMID:32714624;PMID:32482921	PCS		2/3			P	HPO:probinson[2021-10-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0011461	PMID:33269168	PCS		1/1			C	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000316	PMID:33269168;PMID:32714624	PCS		3/3			P	HP:probinson[2021-10-19];HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000954	PMID:25888713;PMID:32714624;PMID:19215037	PCS		12/24			P	HP:probinson[2021-10-19];HPO:probinson[2022-05-08];HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0003826	OMIM:601803	IEA					C	HPO:skoehler[2010-06-20]
OMIM:601803	Pallister-Killian syndrome		HP:0001769	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000158	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001643	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001265	PMID:32714624	PCS		2/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0002751	PMID:25888713	PCS		6/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000175	PMID:25888713;PMID:19215037	PCS		3/23			P	HPO:probinson[2022-05-08];HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000970	OMIM:601803	TAS					P	HPO:skoehler[2015-12-30]
OMIM:601803	Pallister-Killian syndrome		HP:0002079	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0011968	PMID:25888713;PMID:32482921	PCS		16/23			P	HPO:probinson[2021-10-19];HPO:skoehler[2015-12-30];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000293	PMID:32714624	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001263	PMID:19215037	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0001537	PMID:25888713	PCS		5/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0001539	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000966	OMIM:601803	TAS					P	HPO:skoehler[2015-12-30]
OMIM:601803	Pallister-Killian syndrome		HP:0000047	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000960	PMID:33269168	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0004768	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0008947	PMID:25888713	PCS	HP:0003623	20/22			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0001596	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000023	PMID:25888713	PCS		2/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000260	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0009085	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0001629	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0012098	PMID:19215037	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0005949	PMID:32482921	PCS		1/1			P	HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000653	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000256	PMID:32714624;OMIM:601803	PCS		11/12			P	HPO:skoehler[2010-06-20];HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0002558	PMID:25888713;PMID:19215037	PCS		10/22			P	HPO:probinson[2022-05-08];HPO:iea[2009-02-17];HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000776	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0009803	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0032989	PMID:19215037	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0008936	PMID:32714624	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0000154	PMID:32714624;PMID:19215037	PCS		2/3			P	HP:probinson[2021-10-19];HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0000431	PMID:32714624;OMIM:601803	PCS		11/12			P	HP:probinson[2021-10-19];HPO:probinson[2012-05-01]
OMIM:601803	Pallister-Killian syndrome		HP:0000270	PMID:25888713	PCS	HP:0003593	12/19			P	HPO:probinson[2021-06-28]
OMIM:601803	Pallister-Killian syndrome		HP:0000151	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0005280	PMID:32714624	PCS		2/2			P	HPO:probinson[2012-05-01];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0032988	PMID:32482921;PMID:32714624;PMID:19215037	PCS		3/4			P	HPO:probinson[2021-10-19];HP:probinson[2021-10-19];HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0001639	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0007572	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0002209	PMID:32482921;PMID:32714624	PCS		2/3			P	HPO:probinson[2021-10-19];HP:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0200055	PMID:19215037	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0001631	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0001510	PMID:32714624;PMID:19215037	PCS		2/3			P	HP:probinson[2021-10-19];HPO:probinson[2022-05-08]
OMIM:601803	Pallister-Killian syndrome		HP:0000028	PMID:25888713;PMID:32714624	PCS		5/15	MALE		P	HPO:probinson[2021-06-28];HPO:iea[2009-02-17];HPO:probinson[2021-10-19]
OMIM:601803	Pallister-Killian syndrome		HP:0002566	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:601803	Pallister-Killian syndrome		HP:0000545	OMIM:601803	TAS					P	HPO:skoehler[2015-12-30]
OMIM:601803	Pallister-Killian syndrome		HP:0001513	OMIM:601803	IEA					P	HPO:iea[2009-02-17]
OMIM:165660	Oslam syndrome		HP:0002664	OMIM:165660	IEA					P	HPO:skoehler[2010-06-18]
OMIM:165660	Oslam syndrome		HP:0001903	OMIM:165660	IEA					P	HPO:skoehler[2010-06-20]
OMIM:165660	Oslam syndrome		HP:0009466	OMIM:165660	IEA					P	HPO:iea[2009-02-17]
OMIM:165660	Oslam syndrome		HP:0002669	OMIM:165660	TAS					P	HPO:skoehler[2009-02-17]
OMIM:165660	Oslam syndrome		HP:0030084	OMIM:165660	TAS					P	HPO:skoehler[2014-09-21]
OMIM:165660	Oslam syndrome		HP:0000006	OMIM:165660	IEA					I	HPO:iea[2009-02-17]
OMIM:165660	Oslam syndrome		HP:0002974	OMIM:165660	IEA					P	HPO:iea[2009-02-17]
OMIM:615862	Nephronophthisis 18		HP:0003774	PMID:24882706	PCS	HP:0011463	6/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0001396	PMID:24882706	PCS		2/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0000486	PMID:24882706	PCS		1/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0001970	PMID:24882706	PCS		6/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0000090	PMID:24882706	PCS		6/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0000092	PMID:24882706	PCS		6/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0032118	PMID:24882706	PCS		1/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0006580	PMID:24882706	PCS		1/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0000822	PMID:24882706	PCS		2/6			P	HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0000007	PMID:24882706	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0000238	PMID:24882706	PCS		1/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0001249	PMID:24882706	PCS		2/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:615862	Nephronophthisis 18		HP:0004722	PMID:24882706	PCS		6/6			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-25]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0003676	OMIM:125250	TAS					C	HPO:skoehler[2017-07-13]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000486	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0003198	OMIM:125250	TAS					P	HPO:skoehler[2013-01-22]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0001271	OMIM:125250	IEA					P	HPO:skoehler[2019-09-07]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0001251	OMIM:125250	PCS		HP:0040283			P	HPO:probinson[2012-04-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0011463	PMID:12566046	PCS		1/1			C	HPO:probinson[2022-10-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0007663	OMIM:125250	TAS					P	HPO:skoehler[2015-07-26]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0007641	PMID:12566046	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000576	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000552	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000650	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0006958	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0001288	OMIM:125250	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000408	OMIM:125250	PCS					P	HPO:probinson[2012-04-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000508	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000602	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0009830	OMIM:125250	TAS					P	HPO:skoehler[2013-01-22]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000648	PMID:12566046	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000505	PMID:12566046	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000603	PMID:12566046	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000642	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0001257	OMIM:125250	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000006	PMID:12566046	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0000666	OMIM:125250	IEA					P	HPO:iea[2009-02-17]
OMIM:125250	Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy		HP:0003557	OMIM:125250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619080	Kilquist syndrome		HP:0000341	PMID:30740830;PMID:32754646	PCS		2/2			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0003577	PMID:30740830	PCS		1/1			C	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0005211	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0500239	PMID:32754646	PCS		1/1			P	HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0002020	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0001290	PMID:32754646	PCS	HP:0003593	1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0012450	PMID:32754646	PCS		1/1			P	HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000217	PMID:32754646	PCS		1/1			P	HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0001347	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000154	PMID:32754646	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0001344	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000453	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0008619	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0002673	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0011968	PMID:30740830;PMID:32754646	PCS		2/2			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0004691	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0011822	PMID:32754646	PCS		1/1			P	HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0012736	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000007	PMID:30740830	PCS					I	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000768	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000685	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000369	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000303	PMID:30740830;PMID:32754646	PCS		2/2			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000402	PMID:30740830	PCS		1/1			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0002566	PMID:32754646	PCS		1/1			P	HPO:probinson[2020-12-14]
OMIM:619080	Kilquist syndrome		HP:0000522	PMID:30740830;PMID:32754646	PCS		2/2			P	HPO:probinson[2020-12-14];HPO:probinson[2020-12-14];HPO:probinson[2020-12-14]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000365	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000486	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0006628	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001371	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000160	PMID:21358632	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002020	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0012745	OMIM:224690	TAS					P	HPO:skoehler[2014-03-24]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0010886	OMIM:224690	IEA					P	HPO:skoehler[2018-10-08]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0006591	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002937	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0012471	PMID:21358632	PCS		3/4			P	HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002816	PMID:21358632	PCS		3/4			P	HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000911	OMIM:224690	TAS					P	HPO:probinson[2012-06-05]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002857	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001522	PMID:21358632	PCS		2/4			C	HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000237	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000175	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000252	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000054	PMID:21358632	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000376	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002673	OMIM:224690	IEA					P	HPO:skoehler[2018-10-08]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002750	PMID:21358632	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0003561	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001382	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0003042	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000691	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0010554	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0012385	OMIM:224690	TAS					P	HPO:skoehler[2013-10-22]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000327	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000007	PMID:21358632	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000527	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0004209	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000768	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000883	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000369	PMID:21358632	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000963	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000049	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0003577	PMID:21358632	PCS		4/4			C	HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001795	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000581	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000064	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001508	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0008551	PMID:21358632	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001547	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0008872	PMID:21358632	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0006498	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000218	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000059	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000895	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000773	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000413	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001623	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0004279	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001762	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002970	OMIM:224690	IEA					P	HPO:iea[2012-02-25]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0003187	PMID:21358632	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002098	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0003100	PMID:21358632	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002097	PMID:21358632	PCS	HP:0003577	1/3			P	HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0009473	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001518	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0006443	PMID:21358632	PCS		3/3			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0008665	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002007	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0001511	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0200055	OMIM:224690	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000028	PMID:21358632	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0000347	PMID:21358632;OMIM:224690	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:224690	Meier-Gorlin syndrome 1		HP:0002644	OMIM:224690	IEA					P	HPO:iea[2009-02-17]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0001792	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0004322	PMID:36282599;PMID:36299998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0001252	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0003593	PMID:36282599;PMID:36299998	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0008070	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000639	PMID:36282599;PMID:36299998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000957	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0008499	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0007663	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000337	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000414	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000678	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0008897	PMID:36282599;PMID:36299998	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0025435	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000774	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0006236	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0001169	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0003300	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0002673	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0004474	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0003100	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0005484	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000926	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000426	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000568	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000007	PMID:36282599	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000883	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0001414	PMID:36299998	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000325	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620601	Garg-Mishra progeroid syndrome		HP:0000347	PMID:36282599	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001695	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001332	PMID:35147173	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001250	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001252	PMID:35147173	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001790	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0003593	PMID:35147173	PCS		1/4			C	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0000639	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0007663	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001522	PMID:35147173	PCS		2/4			C	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0000873	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0000710	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0003623	PMID:35147173	PCS		2/4			C	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0002059	PMID:35147173	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0002376	PMID:35147173	PCS		1/1			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0009806	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0011968	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0025676	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0011924	PMID:35147173	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001263	PMID:35147173	PCS		1/1			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0005484	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0011664	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0011923	PMID:35147173	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0011504	PMID:35147173	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0034197	PMID:35147173	PCS		1/4			C	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0034295	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001639	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0000407	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001518	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0007110	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001955	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0000007	PMID:35147173	PCS					I	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0008347	PMID:35147173	PCS		1/1			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0200134	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0003811	PMID:35147173	PCS		1/4			C	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0002104	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0000863	PMID:35147173	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620167	Combined oxidative phosphorylation deficiency 57		HP:0001336	PMID:35147173	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002421	PMID:25558065	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000121	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001374	PMID:25558065	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002540	PMID:25558065	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002188	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000089	OMIM:617913	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002783	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0003355	PMID:25558065	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001250	PMID:25558065	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001252	PMID:25558065	PCS		2/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0003593	PMID:25558065	PCS		3/3			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002020	PMID:25558065	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0012444	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000518	PMID:25558065	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000938	PMID:25558065	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-28];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0007068	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000218	PMID:25558065	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002656	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001744	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001920	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001265	PMID:25558065	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000252	PMID:25558065	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002015	OMIM:617913	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0003761	OMIM:617913	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001344	PMID:25558065	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0011968	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0011344	PMID:25558065	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0032988	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002902	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000822	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000007	PMID:25558065	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000648	PMID:25558065	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002900	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0002901	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001257	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0001510	PMID:25558065	PCS		1/3			P	HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000347	PMID:25558065	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-28]
OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		HP:0000126	PMID:25558065	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-28]
OMIM:190400	Trigeminal neuralgia		HP:0000006	OMIM:190400	TAS					I	HPO:skoehler[2013-05-29]
OMIM:190400	Trigeminal neuralgia		HP:0100661	OMIM:190400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0002015	OMIM:614229	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0007979	PMID:21835308	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0002078	PMID:21835308	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0001288	PMID:21835308	PCS		2/2			P	HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0001272	PMID:21835308	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0001260	PMID:21835308	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0001263	PMID:21835308	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0001251	PMID:21835308	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0002070	PMID:21835308	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0011463	PMID:21835308	PCS		2/2			C	HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0007772	PMID:21835308	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0000007	PMID:21835308	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0003677	PMID:21835308	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:614229	Spinocerebellar ataxia, autosomal recessive 11		HP:0006855	PMID:21835308	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:613546	Aromatase deficiency		HP:0003577	PMID:17164303	IEA		4/4			C	HPO:probinson[2022-03-27]
OMIM:613546	Aromatase deficiency		HP:0002750	PMID:17164303	PCS		3/3			P	HPO:probinson[2013-02-23];HPO:probinson[2020-07-24]
OMIM:613546	Aromatase deficiency		HP:0000815	OMIM:613546	TAS					P	HPO:probinson[2013-02-23]
OMIM:613546	Aromatase deficiency		HP:0000007	PMID:17164303	PCS					I	HPO:probinson[2013-02-23];HPO:probinson[2020-07-24]
OMIM:613546	Aromatase deficiency		HP:0010458	PMID:17164303	PCS					P	HPO:probinson[2013-02-23];HPO:probinson[2020-07-24]
OMIM:613546	Aromatase deficiency		HP:0000138	PMID:17164303	PCS					P	HPO:probinson[2013-02-23];HPO:probinson[2020-07-24]
OMIM:613546	Aromatase deficiency		HP:0000786	OMIM:613546	TAS					P	HPO:probinson[2013-02-23]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0001254	PMID:21675912	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0000121	OMIM:143880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0002013	OMIM:143880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0012408	PMID:21675912	PCS		10/10			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0031817	PMID:21675912	PCS		5/5			P	HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0001252	PMID:21675912	PCS		6/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0003593	PMID:21675912	PCS		8/8			C	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0002150	PMID:21675912	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0003072	PMID:21675912	PCS		10/10			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0001508	PMID:21675912	PCS		5/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0001944	PMID:21675912	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0000007	PMID:21675912	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0001824	OMIM:143880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0000103	PMID:21675912	PCS		7/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:143880	Hypercalcemia, infantile, 1		HP:0000787	OMIM:143880	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:114700	Carabelli anomaly of maxillary molar teeth		HP:0000164	OMIM:114700	IEA					P	HPO:iea[2009-02-17]
OMIM:114700	Carabelli anomaly of maxillary molar teeth		HP:0011077	PMID:14933364	TAS					P	HPO:nvasilevsky[2019-03-12]
OMIM:114700	Carabelli anomaly of maxillary molar teeth		HP:0001426	PMID:5079106	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:114700	Carabelli anomaly of maxillary molar teeth		HP:0006358	PMID:5079106	TAS					P	HPO:nvasilevsky[2019-03-12]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0002751	OMIM:146720	IEA					P	HPO:iea[2009-02-17]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0008064	OMIM:146720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0000293	OMIM:146720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0000218	OMIM:146720	IEA					P	HPO:iea[2009-02-17]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0001763	OMIM:146720	IEA					P	HPO:iea[2009-02-17]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0000006	OMIM:146720	IEA					I	HPO:iea[2009-02-17]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0000765	OMIM:146720	IEA					P	HPO:iea[2009-02-17]
OMIM:146720	Ichthyosis-Cheek-Eyebrow syndrome		HP:0005338	OMIM:146720	IEA					P	HPO:iea[2009-02-17]
OMIM:159600	Myoclonic epilepsy, Hartung type		HP:0002123	OMIM:159600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:159600	Myoclonic epilepsy, Hartung type		HP:0000006	OMIM:159600	TAS					I	HPO:skoehler[2012-09-16]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0003621	OMIM:608600	IEA					C	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0002155	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0000287	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0000991	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0003011	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0002240	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0003074	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0009003	OMIM:608600	TAS					P	HPO:probinson[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0000822	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0001735	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0009125	OMIM:608600	TAS					P	HPO:probinson[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0000956	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0009017	OMIM:608600	TAS					P	HPO:probinson[2012-07-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0003635	OMIM:608600	TAS					P	HPO:probinson[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0001015	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0000006	OMIM:608600	IEA					I	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0000468	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0000831	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:608600	Lipodystrophy, familial partial, type 1		HP:0001677	OMIM:608600	IEA					P	HPO:iea[2009-02-17]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0003596	PMID:26553276	PCS		1/4			C	HPO:probinson[2023-06-10]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0003487	PMID:26553276	PCS		1/3			P	HPO:skoehler[2017-07-13]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0003484	PMID:26553276	PCS		0/8			P	HPO:probinson[2023-06-10]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0002395	PMID:26553276	PCS		4/4			P	HPO:probinson[2023-06-10]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0007340	PMID:26553276	PCS		4/4			P	HPO:probinson[2023-06-10]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0011462	PMID:26553276	PCS		3/4			C	HPO:probinson[2023-06-10]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0007210	PMID:26553276	PCS		1/4			P	HPO:skoehler[2017-07-13]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0000007	PMID:26553276	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0001258	PMID:26553276	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:617046	Spastic paraplegia 77, autosomal recessive		HP:0003677	PMID:26553276	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0030502	PMID:23707145	PCS		1/6			P	HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0003621	PMID:23707145	PCS		2/6			C	HPO:probinson[2022-11-05];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0002345	PMID:23707145	PCS		2/6			P	HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0003596	PMID:23707145	PCS		2/6			C	HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0001123	PMID:23707145	PCS		4/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0011506	PMID:23707145	PCS		1/6			P	HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0002066	PMID:23707145	PCS		2/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0002352	PMID:23707145	PCS					P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0002070	PMID:23707145	PCS		6/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0011463	PMID:23707145	PCS		1/6			C	HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0000007	PMID:23707145	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0025710	PMID:23707145	PCS		1/6			C	HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0002315	PMID:23707145	PCS		3/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0001138	PMID:23707145	PCS		2/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-05]
OMIM:615651	Leukoencephalopathy with ataxia		HP:0000533	PMID:23707145	PCS		1/6			P	HPO:probinson[2022-11-05]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0008209	PMID:24808023	PCS		5/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0003676	PMID:24808023	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0003596	PMID:24808023	PCS		1/6			C	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0001332	PMID:24808023	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0002186	PMID:24808023	PCS		1/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0001272	PMID:24808023	PCS		5/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0001251	PMID:24808023	PCS		4/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0002180	PMID:24808023	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0000716	PMID:24808023	PCS		3/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0000639	PMID:24808023	PCS		3/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0011463	PMID:24808023	PCS		1/6			C	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0011462	PMID:24808023	PCS		3/6			C	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0006970	PMID:24808023	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0001324	PMID:24808023	PCS		2/6			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0003688	PMID:24808023	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0001347	PMID:24808023	PCS		5/6			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0002378	PMID:24808023	PCS		1/6			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0003621	PMID:24808023	PCS		1/6			C	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0006956	PMID:24808023	PCS		2/6			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0003487	PMID:24808023	PCS		4/6			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0002376	PMID:24808023	PCS		6/6			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0001260	PMID:24808023	PCS		2/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0002352	PMID:24808023	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0002371	PMID:24808023	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0000709	PMID:24808023	PCS		1/6			P	HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0000726	PMID:24808023	PCS		1/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0006980	PMID:24808023	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0000007	PMID:24808023	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-06]
OMIM:615889	Leukoencephalopathy, progressive, with ovarian failure		HP:0001257	PMID:24808023	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-06]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000286	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000483	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001374	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000365	OMIM:617052	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0004322	PMID:28062395;PMID:27346687	PCS		5/8			P	HPO:probinson[2023-04-18];HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0100255	PMID:28062395	PCS		2/4			P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0100840	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0011463	PMID:28062395	PCS		1/4			C	HPO:probinson[2023-04-18];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0040012	PMID:28062395;PMID:27346687	PCS		0/7			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0006276	PMID:28062395	PCS		3/3			P	HPO:probinson[2023-04-18];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000316	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0005528	PMID:28062395;PMID:27346687	PCS		7/8			P	HPO:probinson[2023-04-18];HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000752	OMIM:617052	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000556	PMID:28062395;PMID:27346687	PCS		2/8			P	HPO:probinson[2023-04-18];HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0003623	PMID:28062395	PCS		3/4			C	HPO:probinson[2023-04-18];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000494	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000252	PMID:27346687	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0011968	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001382	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000490	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001263	PMID:28062395	PCS		3/8			P	HPO:probinson[2023-04-18];HPO:skoehler[2019-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000691	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001738	PMID:28062395	PCS		2/4			P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0004808	PMID:27346687	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000007	PMID:27346687	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000964	PMID:28062395	PCS		1/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0008404	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000962	PMID:27346687	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001792	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0009719	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000540	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0100790	OMIM:617052	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001270	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0008070	OMIM:617052	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001508	PMID:28062395	PCS		1/4			P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0002719	PMID:28062395	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001903	PMID:28062395	PCS		4/4			P	HPO:probinson[2023-04-18];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0006297	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0002714	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000378	PMID:28062395	PCS		1/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000155	PMID:27346687	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0011904	PMID:28062395	PCS		3/4			P	HPO:probinson[2023-04-18];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0031413	PMID:27346687	PCS		0/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0033757	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0100512	PMID:28062395	PCS		3/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0100513	PMID:28062395	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000705	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001915	PMID:28062395	PCS		1/4			P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000668	OMIM:617052	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617052	Bone marrow failure syndrome 3		HP:0005518	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0007973	PMID:28062395	PCS		1/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001511	PMID:27346687	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001873	PMID:28062395	PCS		3/4			P	HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000028	OMIM:617052	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000347	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0000545	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001876	PMID:28062395;PMID:27346687	PCS		6/8			P	HPO:probinson[2023-04-18];HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617052	Bone marrow failure syndrome 3		HP:0004349	OMIM:617052	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617052	Bone marrow failure syndrome 3		HP:0001875	PMID:28062395	PCS		4/4			P	HPO:probinson[2023-04-18]
OMIM:223100	Lactase persistence/nonpersistence		HP:0002014	PMID:12915462	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-13]
OMIM:223100	Lactase persistence/nonpersistence		HP:0003621	PMID:12915462	PCS					C	HPO:probinson[2021-02-13]
OMIM:223100	Lactase persistence/nonpersistence		HP:0025130	PMID:11788828	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-17]
OMIM:223100	Lactase persistence/nonpersistence		HP:0011463	PMID:12915462	PCS					C	HPO:probinson[2021-02-13]
OMIM:223100	Lactase persistence/nonpersistence		HP:0011462	PMID:12915462	PCS					C	HPO:probinson[2021-02-13]
OMIM:223100	Lactase persistence/nonpersistence		HP:0033589	PMID:12915462	PCS					P	HPO:probinson[2021-02-13]
OMIM:223100	Lactase persistence/nonpersistence		HP:0004789	PMID:12915462	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-13]
OMIM:223100	Lactase persistence/nonpersistence		HP:0002027	PMID:12915462	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:223100	Lactase persistence/nonpersistence		HP:0000006	PMID:11788828	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-17]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0001771	PMID:31575858	PCS		4/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0001374	PMID:31575858	PCS	HP:0003577	1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0003577	PMID:31575858	PCS		1/6			C	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0001377	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0025169	PMID:31575858	PCS		2/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0001252	PMID:31575858	PCS		6/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0030891	PMID:31575858	PCS		3/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0003593	PMID:31575858	PCS		5/6			C	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0033204	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0005590	PMID:31575858	PCS		2/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0012368	PMID:31575858	PCS		5/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000639	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000957	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000739	PMID:31575858	PCS		4/4			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0002938	PMID:31575858	PCS		4/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0020045	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000219	PMID:31575858	PCS		6/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000455	PMID:31575858	PCS		4/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0001566	PMID:31575858	PCS		2/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0011081	PMID:31575858	PCS		4/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000336	PMID:31575858	PCS		6/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0002650	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0001047	PMID:31575858	PCS		2/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0002395	PMID:31575858	PCS		4/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0002172	PMID:31575858	PCS		6/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0012378	PMID:31575858	PCS		6/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0010535	PMID:31575858	PCS		2/2			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0500093	PMID:31575858	PCS		2/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0032012	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000965	PMID:31575858	PCS		6/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000007	PMID:31575858	IEA					I	HPO:probinson[2022-03-03];HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000601	PMID:31575858	PCS		4/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000689	PMID:31575858	PCS		4/6			P	HPO:probinson[2022-03-03]
OMIM:619719	Intellectual disability and myopathy syndrome		HP:0000565	PMID:31575858	PCS		1/6			P	HPO:probinson[2022-03-03];HPO:probinson[2022-07-10]
OMIM:300915	Microphthalmia, syndromic 13		HP:0002751	PMID:24993872	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0000252	PMID:24993872	PCS		3/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0003577	PMID:24993872	PCS		4/4			C	HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0004322	PMID:24993872	PCS		3/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0001263	PMID:24993872	PCS		4/4			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0000482	PMID:24993872	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0040080	PMID:24993872	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0012043	PMID:24993872	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0000508	PMID:24993872	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0000568	PMID:24993872	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0000612	PMID:24993872	PCS		4/4			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0001417	PMID:24993872	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0000565	PMID:24993872	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0001249	PMID:24993872	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0006304	PMID:24993872	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:300915	Microphthalmia, syndromic 13		HP:0000567	PMID:24993872	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0032209	PMID:26854926	PCS		0/1			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0003621	PMID:34956927	PCS		1/1			C	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0003388	PMID:26854926	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0011788	PMID:34956927	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0033076	PMID:34956927	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0033077	PMID:26854926	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0031097	PMID:34956927;PMID:26854926	PCS		0/2			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0034288	PMID:26854926;PMID:34956927	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0000007	PMID:26854926	PCS					I	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0008247	PMID:34956927	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0001324	PMID:26854926	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0033192	PMID:26854926	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620198	Thyroid hormone metabolism, abnormal, 3		HP:0002027	PMID:26854926	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:227400	Factor V deficiency		HP:0000132	OMIM:227400	TAS					P	HPO:probinson[2009-02-17]
OMIM:227400	Factor V deficiency		HP:0001892	OMIM:227400	IEA					P	HPO:iea[2009-02-17]
OMIM:227400	Factor V deficiency		HP:0003225	OMIM:227400	IEA					P	HPO:iea[2009-02-17]
OMIM:227400	Factor V deficiency		HP:0008151	OMIM:227400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:227400	Factor V deficiency		HP:0005542	OMIM:227400	IEA					P	HPO:iea[2009-02-17]
OMIM:227400	Factor V deficiency		HP:0003010	OMIM:227400	IEA					P	HPO:iea[2009-02-17]
OMIM:227400	Factor V deficiency		HP:0000007	OMIM:227400	IEA					I	HPO:iea[2009-02-17]
OMIM:227400	Factor V deficiency		HP:0000978	OMIM:227400	TAS					P	HPO:probinson[2013-03-12]
OMIM:227400	Factor V deficiency		HP:0000421	OMIM:227400	TAS					P	HPO:probinson[2009-02-17]
OMIM:227400	Factor V deficiency		HP:0003645	OMIM:227400	TAS					P	HPO:probinson[2009-02-17]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0003235	OMIM:250850	PCS					P	HPO:probinson[2012-04-11]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0011096	OMIM:250850	TAS					P	HPO:skoehler[2012-10-17]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0001332	OMIM:250850	PCS					P	HPO:probinson[2012-04-11]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0100812	OMIM:250850	IEA					P	HPO:skoehler[2019-09-07]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0000007	OMIM:250850	PCS					I	HPO:probinson[2012-04-11]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0007305	OMIM:250850	PCS					P	HPO:probinson[2012-04-11]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0001249	OMIM:250850	PCS		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0000006	OMIM:250850	PCS					I	HPO:probinson[2012-04-11]
OMIM:250850	Methionine adenosyltransferase I/III deficiency		HP:0001347	OMIM:250850	PCS					P	HPO:probinson[2012-04-11]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0002465	PMID:24951542	PCS		4/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-31]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0001320	PMID:24951542	PCS		1/1			P	HPO:probinson[2023-01-31]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0003577	PMID:24951542	PCS		4/4			C	HPO:probinson[2023-01-31]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0001250	PMID:24951542	PCS		2/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-31]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0000718	PMID:24951542	PCS		4/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-31]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0001263	PMID:24951542	PCS		4/4		HP:0012828	P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-31]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0011451	PMID:24951542	PCS	HP:0003577	4/4			P	HPO:probinson[2023-01-31]
OMIM:616402	Microcephaly 14, primary, autosomal recessive		HP:0000007	PMID:24951542	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-31]
OMIM:176807	Prostate cancer		HP:0001442	OMIM:176807	IEA					I	HPO:skoehler[2019-02-22]
OMIM:176807	Prostate cancer		HP:0012125	OMIM:176807	TAS					P	HPO:probinson[2013-08-11]
OMIM:176807	Prostate cancer		HP:0000006	OMIM:176807	TAS					I	HPO:skoehler[2013-08-18]
OMIM:602477	Febrile seizures, familial, 2		HP:0002069	OMIM:602477	IEA					P	HPO:iea[2009-02-17]
OMIM:602477	Febrile seizures, familial, 2		HP:0002373	OMIM:602477	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602477	Febrile seizures, familial, 2		HP:0010819	OMIM:602477	TAS					P	HPO:skoehler[2013-04-18]
OMIM:602477	Febrile seizures, familial, 2		HP:0010818	OMIM:602477	IEA					P	HPO:iea[2009-02-17]
OMIM:602477	Febrile seizures, familial, 2		HP:0003593	OMIM:602477	TAS					C	HPO:probinson[2013-04-05]
OMIM:602477	Febrile seizures, familial, 2		HP:0000006	PMID:20437590	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:218800	Crigler-Najjar syndrome, type I		HP:0008282	PMID:8690398;PMID:37602038	PCS		58/58			P	HPO:probinson[2024-03-08];HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:218800	Crigler-Najjar syndrome, type I		HP:0001298	PMID:8690398	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-26]
OMIM:218800	Crigler-Najjar syndrome, type I		HP:0003577	PMID:8690398;PMID:37602038	PCS		11/11			C	HPO:probinson[2024-03-08];HPO:probinson[2022-07-20]
OMIM:218800	Crigler-Najjar syndrome, type I		HP:0001343	PMID:8690398	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:218800	Crigler-Najjar syndrome, type I		HP:0000007	PMID:8690398	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:218800	Crigler-Najjar syndrome, type I		HP:0002910	PMID:37602038	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:218800	Crigler-Najjar syndrome, type I		HP:0000952	PMID:8690398;PMID:37602038	PCS		58/58			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-26];HPO:probinson[2024-03-08]
OMIM:260005	5-@oxoprolinase deficiency		HP:0002014	OMIM:260005	IEA					P	HPO:iea[2009-02-17]
OMIM:260005	5-@oxoprolinase deficiency		HP:0003137	OMIM:260005	TAS					P	HPO:skoehler[2015-01-21]
OMIM:260005	5-@oxoprolinase deficiency		HP:0002013	OMIM:260005	IEA					P	HPO:iea[2009-02-17]
OMIM:260005	5-@oxoprolinase deficiency		HP:0004387	OMIM:260005	IEA					P	HPO:iea[2009-02-17]
OMIM:260005	5-@oxoprolinase deficiency		HP:0410132	PMID:10094443	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:260005	5-@oxoprolinase deficiency		HP:0040142	OMIM:260005	TAS					P	HPO:skoehler[2015-01-21]
OMIM:260005	5-@oxoprolinase deficiency		HP:0008672	OMIM:260005	TAS					P	HPO:skoehler[2015-04-18]
OMIM:260005	5-@oxoprolinase deficiency		HP:0000007	OMIM:260005	IEA					I	HPO:iea[2009-02-17]
OMIM:260005	5-@oxoprolinase deficiency		HP:0002027	OMIM:260005	IEA					P	HPO:iea[2009-02-17]
OMIM:260005	5-@oxoprolinase deficiency		HP:0000006	OMIM:260005	TAS					I	HPO:skoehler[2017-07-13]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000341	PMID:30427554	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0003774	PMID:30427554	PCS		4/4			P	HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000252	PMID:30427554	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0002188	PMID:30427554	PCS		1/3			P	HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000486	PMID:30427554	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000365	PMID:30427554	PCS		2/4			P	HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000100	PMID:30427554	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0002120	PMID:30427554	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0001250	PMID:30427554	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000097	PMID:30427554	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0001263	PMID:30427554	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000790	OMIM:618349	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0001252	PMID:30427554	PCS		4/4			P	HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0032046	PMID:30427554	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0003073	OMIM:618349	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000093	PMID:30427554	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000092	OMIM:618349	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0012444	PMID:30427554	PCS		3/3			P	HPO:probinson[2022-12-21];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0011463	PMID:30427554	PCS		3/4			C	HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0006297	PMID:30427554	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0001317	OMIM:618349	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0000007	PMID:30427554	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618349	Galloway-Mowat syndrome 8		HP:0003623	PMID:30427554	PCS		1/4			C	HPO:probinson[2022-12-21]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0003510	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0002059	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0000365	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0002376	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0002063	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0011410	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0011923	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0011951	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0000639	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0001518	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0040288	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0012692	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0000007	PMID:30607703	PCS					I	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0000648	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0002878	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0001511	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0001510	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0002643	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619057	Combined oxidative phosphorylation deficiency 51		HP:0001336	PMID:30607703	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:616364	White-Sutton syndrome		HP:0000483	PMID:32359026;PMID:26739615;PMID:35052493;PMID:31782611;PMID:34206215;PMID:26942287	PCS		15/45			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000486	PMID:27148570;PMID:33909211;PMID:30879264;PMID:34645992;PMID:26739615;PMID:35052493;PMID:31782611;PMID:25694107;PMID:31347273;PMID:26942287;PMID:28480548	PCS		19/51			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0004322	PMID:34215294;PMID:32359026;PMID:30879264;PMID:26739615;PMID:35052493;PMID:26942287;PMID:28480548	PCS		10/47			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002263	PMID:33377604;PMID:30879264;PMID:26739615;PMID:35052493;PMID:31347273;PMID:26763879;PMID:25694107;PMID:31136090;PMID:32345733	PCS		16/20			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002384	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002020	PMID:26739615;PMID:35052493;PMID:26942287;PMID:28480548	PCS		6/43			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0003593	PMID:26739615;PMID:31782611	PCS		15/18			C	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001290	PMID:27148570;PMID:25533962;PMID:34215294;PMID:26739615;PMID:35052493;PMID:34206215	PCS		17/25			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000081	PMID:26739615	PCS		2/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0033725	PMID:25533962	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000639	PMID:26942287	PCS		1/21			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000356	PMID:25533962	PCS		1/2			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000752	PMID:26942287	PCS		4/25			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000510	PMID:34645992;PMID:26739615;PMID:35052493;PMID:31782611	PCS		4/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002019	PMID:33909211;PMID:33277917;PMID:35052493;PMID:26942287;PMID:28480548	PCS		13/42			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000512	PMID:25533962	PCS		1/2			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000358	PMID:26739615;PMID:35052493	PCS		7/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002553	PMID:33377604;PMID:30879264;PMID:26739615;PMID:35052493;PMID:34206215;PMID:31347273;PMID:26763879;PMID:31136090;PMID:28480548	PCS		10/21			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000494	PMID:34215294;PMID:33277917;PMID:26739615;PMID:35052493;PMID:25694107;PMID:31136090;PMID:28480548	PCS		14/25			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000252	PMID:27148570;PMID:34215294;PMID:30879264;PMID:33277917;PMID:34645992;PMID:26739615;PMID:35052493;PMID:31782611;PMID:34206215;PMID:25694107;PMID:28480548;PMID:26763879;PMID:26942287;PMID:31136090	PCS		51/89			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002033	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0011800	PMID:34215294;PMID:32359026;PMID:30879264;PMID:33277917;PMID:35052493;PMID:26739615;PMID:34206215;PMID:25694107;PMID:28480548;PMID:32345733;PMID:34133408;PMID:33377604;PMID:26763879;PMID:31136090	PCS		23/29			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0100025	PMID:26942287	PCS		6/25			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0034392	PMID:27148570;PMID:35052493	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000649	PMID:25533962	PCS		1/2			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000407	PMID:27148570;PMID:34215294;PMID:30879264;PMID:34645992;PMID:33277917;PMID:26739615;PMID:35052493;PMID:31782611;PMID:34206215;PMID:32345733;PMID:28480548;PMID:31136090;PMID:26942287	PCS		21/66			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000403	PMID:30879264;PMID:34645992;PMID:35052493;PMID:26942287	PCS		13/21			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000648	PMID:35052493;PMID:26739615;PMID:31782611;PMID:26942287	PCS		7/17			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000006	PMID:25533962	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000248	PMID:34133408;PMID:32359026;PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215;PMID:26942287;PMID:32345733	PCS		20/51			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000369	PMID:32359026;PMID:33277917;PMID:26739615;PMID:35052493	PCS		6/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000341	PMID:35052493	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0003577	PMID:26739615;PMID:31782611	PCS		2/18			C	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000582	PMID:26739615;PMID:35052493	PCS		2/17			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001156	PMID:34215294;PMID:34645992;PMID:33277917;PMID:26739615;PMID:35052493;PMID:28480548	PCS		9/22			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002365	PMID:30879264;PMID:35052493;PMID:28480548	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001270	PMID:26942287	PCS		13/22			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0008070	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0100033	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0100704	PMID:26739615;PMID:35052493;PMID:31782611	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000737	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000739	PMID:27148570;PMID:32359026;PMID:33909211;PMID:33277917;PMID:35052493;PMID:26942287	PCS		21/46			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000337	PMID:26739615;PMID:35052493	PCS		9/17			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001305	PMID:30879264;PMID:35052493;PMID:26739615	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000612	PMID:25533962	PCS		1/2			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000733	PMID:26942287	PCS		4/25			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000219	PMID:34133408;PMID:33377604;PMID:32359026;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:31136090;PMID:28480548	PCS		20/26			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002119	PMID:34215294;PMID:32359026;PMID:35052493;PMID:31782611;PMID:34206215;PMID:31136090;PMID:28480548	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002515	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0030084	PMID:34215294;PMID:35052493;PMID:31136090;PMID:28480548	PCS		4/16			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000218	PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215	PCS		9/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000455	PMID:33377604;PMID:32359026;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215;PMID:31136090;PMID:28480548	PCS		15/24			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000577	PMID:26739615	PCS		2/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0008619	PMID:25533962	PCS		1/2			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000750	PMID:27148570;PMID:34215294;PMID:32359026;PMID:30879264;PMID:34645992;PMID:33277917;PMID:35052493;PMID:26739615;PMID:31782611;PMID:34206215;PMID:25694107;PMID:28480548;PMID:32345733;PMID:34133408;PMID:26763879;PMID:31347273;PMID:26942287;PMID:31136090	PCS		98/102			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002650	PMID:27148570;PMID:33277917;PMID:34645992;PMID:35052493	PCS		3/15			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000233	PMID:26739615	PCS		3/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001321	PMID:27148570;PMID:32359026;PMID:33277917;PMID:31782611;PMID:34206215;PMID:26942287;PMID:28480548	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000232	PMID:34133408;PMID:33377604;PMID:33277917;PMID:35052493;PMID:34206215;PMID:31136090;PMID:28480548	PCS		13/19			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002373	PMID:35052493;PMID:26942287	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000194	PMID:33377604;PMID:33277917;PMID:26739615;PMID:35052493;PMID:25694107;PMID:31136090;PMID:28480548	PCS		13/20			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000193	PMID:26739615;PMID:35052493	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000470	PMID:33377604;PMID:26739615;PMID:35052493;PMID:34206215	PCS		11/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0025190	PMID:35052493	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001837	PMID:27148570;PMID:32359026;PMID:26739615;PMID:35052493;PMID:34206215;PMID:28480548	PCS		9/19			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000508	PMID:34133408;PMID:33377604;PMID:30879264;PMID:26739615;PMID:35052493;PMID:26763879;PMID:28480548	PCS		7/18			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000744	PMID:30879264;PMID:35052493;PMID:31347273;PMID:26763879;PMID:26942287	PCS		10/13			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0100716	PMID:33277917;PMID:26739615;PMID:35052493;PMID:26942287	PCS		13/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000505	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001159	PMID:27148570;PMID:35052493;PMID:28480548	PCS		3/16			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002645	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0007018	PMID:27148570;PMID:34215294;PMID:27824329;PMID:32359026;PMID:33277917;PMID:35052493;PMID:26942287	PCS		15/19			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000589	PMID:34645992;PMID:35052493	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000347	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000286	PMID:34133408;PMID:33377604;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:26763879;PMID:25694107;PMID:31136090;PMID:28480548	PCS		17/25			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002188	PMID:33277917;PMID:26739615;PMID:35052493;PMID:31782611	PCS		6/15			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0010803	PMID:34133408;PMID:33377604;PMID:33277917;PMID:35052493;PMID:34206215;PMID:31136090;PMID:28480548	PCS		12/19			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001250	PMID:34215294;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:31782611;PMID:34206215;PMID:32345733;PMID:28480548;PMID:34133408;PMID:27824329;PMID:31136090;PMID:26942287	PCS		19/50			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001252	PMID:26739615;PMID:26942287	PCS		8/27			P	HPO:probinson[2022-04-12];HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0012389	PMID:30879264;PMID:35052493	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0045075	PMID:35052493	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000718	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000437	PMID:26739615	PCS		4/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000316	PMID:34215294;PMID:32359026;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215;PMID:25694107;PMID:26763879;PMID:31136090;PMID:28480548	PCS		24/30			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001769	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000158	PMID:34215294;PMID:32359026;PMID:33277917;PMID:35052493;PMID:31136090	PCS		6/14			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001643	PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215	PCS		3/19			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000278	PMID:35052493	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001249	PMID:27148570;PMID:34215294;PMID:32359026;PMID:33909211;PMID:33277917;PMID:34645992;PMID:26739615;PMID:35052493;PMID:31782611;PMID:25694107;PMID:32345733;PMID:28480548;PMID:34133408;PMID:27824329;PMID:33377604;PMID:26763879;PMID:26942287	PCS		88/91			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000297	PMID:33377604;PMID:33277917;PMID:35052493;OMIM:616364	PCS		15/23			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0025573	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000175	PMID:30879264;PMID:34645992;PMID:26739615;PMID:35052493	PCS		5/20			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000054	PMID:33277917;PMID:35052493	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002870	PMID:26739615	PCS		2/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002079	PMID:27148570;PMID:25533962;PMID:34645992;PMID:33277917;PMID:35052493;PMID:31782611;PMID:31136090;PMID:28480548	PCS		11/18			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0011968	PMID:32359026;PMID:30879264;PMID:33277917;PMID:34645992;PMID:26739615;PMID:35052493;PMID:34206215;PMID:26942287;PMID:31136090	PCS		32/51			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001382	PMID:32359026;PMID:34645992;PMID:26739615;PMID:35052493;PMID:26942287	PCS		11/47			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001263	PMID:27148570;PMID:34215294;PMID:32359026;PMID:30879264;PMID:34645992;PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215;PMID:25694107;PMID:28480548;PMID:32345733;PMID:34133408;PMID:25533962;PMID:27824329;PMID:26763879;PMID:26942287;PMID:31136090	PCS		87/88			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002194	PMID:27148570;PMID:34215294;PMID:32359026;PMID:33909211;PMID:33277917;PMID:35052493;PMID:31782611;PMID:34206215;PMID:25694107;PMID:28480548;PMID:32345733;PMID:27824329;PMID:31347273;PMID:26942287	PCS		80/87			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000609	PMID:25533962;PMID:26739615	PCS		3/10			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000729	PMID:27148570;PMID:34215294;PMID:33909211;PMID:32359026;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:31782611;PMID:25694107;PMID:28480548;PMID:27824329;PMID:31347273;PMID:26942287;PMID:31136090	PCS		48/65			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001537	PMID:30879264;PMID:35052493	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000447	PMID:34133408;PMID:32359026;PMID:30879264;PMID:33277917;PMID:35052493;PMID:26739615;PMID:25694107;PMID:26763879;PMID:31136090;PMID:28480548	PCS		14/22			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000322	PMID:33377604;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:31347273;PMID:26942287;PMID:31136090;PMID:28480548	PCS		17/47			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001655	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000540	PMID:34645992;PMID:26739615;PMID:35052493;PMID:31782611;PMID:34206215;PMID:26942287	PCS		21/51			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000023	PMID:30879264;PMID:35052493	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0030674	PMID:31782611	PCS		1/13			C	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0010862	PMID:34215294;PMID:32359026;PMID:30879264;PMID:35052493;PMID:34206215;PMID:31347273;PMID:26942287;PMID:28480548;PMID:32345733	PCS		16/16			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0012803	PMID:35052493;PMID:26739615	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001508	PMID:27148570;PMID:33277917;PMID:26739615;PMID:35052493	PCS		7/18			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002719	PMID:26942287	PCS		6/25			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002714	PMID:34133408;PMID:33377604;PMID:33277917;PMID:35052493;PMID:26739615;PMID:25694107;PMID:26763879;PMID:31347273;PMID:26942287;PMID:31136090;PMID:28480548	PCS		19/49			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0008434	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001500	PMID:27148570;PMID:32359026;PMID:35052493;PMID:26739615;PMID:34206215;PMID:28480548	PCS		8/19			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000776	PMID:33277917;PMID:26739615;PMID:35052493	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0008936	PMID:30879264;PMID:35052493	PCS		8/12			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000396	PMID:33377604;PMID:33277917;PMID:35052493;PMID:26739615;PMID:34206215	PCS		6/15			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000154	PMID:34215294;PMID:30879264;PMID:33277917;PMID:35052493;PMID:26739615;PMID:28480548	PCS		9/17			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002059	PMID:27148570;PMID:34133408;PMID:25533962;PMID:34215294;PMID:35052493;PMID:31782611;PMID:34206215;PMID:31136090;PMID:26942287	PCS		10/17			P	ORCID:0000-0002-0736-9199[2024-08-18];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002572	PMID:27148570;PMID:34645992;PMID:33277917;PMID:35052493;PMID:26942287	PCS		11/19			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002173	PMID:25533962	PCS		1/2			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0000272	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0005280	PMID:34215294;PMID:32359026;PMID:33377604;PMID:30879264;PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215;PMID:26763879;PMID:25694107;PMID:26942287;PMID:31136090	PCS		16/53			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18];HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0011304	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0012760	PMID:34133408;PMID:34215294;PMID:33909211;PMID:33277917;PMID:26739615;PMID:35052493;PMID:31347273;PMID:26763879;PMID:25694107;PMID:26942287;PMID:28480548	PCS		26/35			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000307	PMID:30879264;PMID:26739615;PMID:35052493;PMID:26763879;PMID:31136090;PMID:28480548	PCS		14/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001511	PMID:26942287	PCS	HP:0011461	4/21			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0001357	PMID:35052493;PMID:26942287;PMID:31136090	PCS		4/15			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0002205	PMID:33377604;PMID:30879264;PMID:35052493;PMID:26942287;PMID:28480548	PCS		10/18			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001631	PMID:33277917;PMID:26739615;PMID:35052493;PMID:28480548	PCS		5/19			P	HPO:probinson[2022-04-12];HPO:probinson[2024-08-18];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000028	PMID:33277917;PMID:35052493;PMID:26942287	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000303	PMID:34133408;PMID:32359026;PMID:33277917;PMID:26739615;PMID:35052493;PMID:34206215;PMID:28480548	PCS		8/24			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0000545	PMID:30879264;PMID:34645992;PMID:35052493;PMID:26739615;PMID:31782611;PMID:26942287	PCS		8/43			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12];ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:616364	White-Sutton syndrome		HP:0001513	PMID:26739615;PMID:26942287	PCS		12/26			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0002721	PMID:26739615	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616364	White-Sutton syndrome		HP:0009879	PMID:27148570;PMID:35052493;PMID:28480548	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-08-18]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0002069	PMID:11906506	PCS		12/12			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0032759	PMID:10851389	PCS		1/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0003621	PMID:11906506	PCS		4/12			C	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0003596	PMID:11906506	PCS		1/12			C	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0002266	PMID:10851389	PCS		1/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0002384	PMID:7647791	PCS		6/18			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0011159	PMID:10851389	PCS		4/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0032773	PMID:10851389	PCS		1/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0011158	PMID:10851389;PMID:7647791	PCS		13/29			P	HPO:probinson[2012-07-31];HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0032864	PMID:11906506	PCS		4/12			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0032898	PMID:10851389	PCS		1/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0032810	PMID:10851389	PCS		3/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0012005	PMID:10851389	PCS		1/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0011161	PMID:10851389	PCS		1/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0011165	PMID:10851389	PCS		2/11			P	HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0011462	PMID:11906506	PCS		7/12			C	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0007334	PMID:7647791	PCS		12/18			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0002349	PMID:7647791;PMID:11906506	PCS		15/30			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:600512	Epilepsy, familial temporal lobe, 1		HP:0000006	PMID:10851389	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:158250	NONDISJUNCTION		HP:0000144	OMIM:158250	IEA					P	HPO:iea[2009-02-17]
OMIM:158250	NONDISJUNCTION		HP:0002916	OMIM:158250	IEA					P	HPO:iea[2009-02-17]
OMIM:158250	NONDISJUNCTION		HP:0000007	OMIM:158250	IEA					I	HPO:iea[2009-02-17]
OMIM:158250	NONDISJUNCTION		HP:0000006	OMIM:158250	IEA					I	HPO:iea[2009-02-17]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0003676	OMIM:616370	IEA					C	HPO:skoehler[2018-10-08]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0001344	PMID:25539947	PCS		6/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0002376	PMID:25539947	PCS		4/6			P	HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0003593	PMID:25539947	PCS		6/6			C	HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0001290	OMIM:616370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0012736	PMID:25539947	PCS		2/6			P	HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0011923	PMID:25539947	PCS		1/1			P	HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0031358	OMIM:616370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0000639	OMIM:616370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0002518	OMIM:616370	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0000007	PMID:25539947	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0000648	PMID:25539947	PCS		6/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0000505	OMIM:616370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0002415	OMIM:616370	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0001257	PMID:25539947	PCS		6/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-03-10]
OMIM:616370	Multiple mitochondrial dysfunctions syndrome 4		HP:0001347	OMIM:616370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:259690	Osteopenia and sparse hair		HP:0000271	OMIM:259690	IEA					P	HPO:iea[2009-02-17]
OMIM:259690	Osteopenia and sparse hair		HP:0001382	OMIM:259690	IEA					P	HPO:iea[2009-02-17]
OMIM:259690	Osteopenia and sparse hair		HP:0000938	OMIM:259690	IEA					P	HPO:iea[2009-02-17]
OMIM:259690	Osteopenia and sparse hair		HP:0001252	OMIM:259690	TAS		20/20			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01];HPO:iea[2009-02-17]
OMIM:259690	Osteopenia and sparse hair		HP:0000007	OMIM:259690	IEA					I	HPO:iea[2009-02-17]
OMIM:259690	Osteopenia and sparse hair		HP:0001249	OMIM:259690	IEA					P	HPO:iea[2009-02-17]
OMIM:259690	Osteopenia and sparse hair		HP:0008070	OMIM:259690	IEA					P	HPO:iea[2009-02-17]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0000132	OMIM:614201	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0011871	PMID:19549989	PCS		0/1			P	HPO:probinson[2023-03-07]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0003593	PMID:19549989	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0003010	PMID:19549989	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0008320	PMID:19549989	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0031364	PMID:19549989	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-07]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0000007	PMID:19549989	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0000978	OMIM:614201	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0000421	OMIM:614201	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614201	Bleeding disorder, platelet-type, 11		HP:0011873	PMID:19549989	PCS		0/1			P	HPO:probinson[2023-03-07]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002069	PMID:33242881	PCS		2/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002322	PMID:33242881	PCS		2/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002067	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002188	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0001332	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0025269	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0001251	PMID:33242881	PCS		4/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0003593	PMID:33242881	PCS		2/10			C	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0001270	PMID:33242881	PCS		9/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002080	PMID:33242881	PCS		4/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0100034	PMID:33242881	PCS		3/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0007082	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0011463	PMID:33242881	PCS		8/10			C	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0000739	PMID:33242881	PCS		3/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0000733	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002518	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0001249	PMID:33242881	PCS		9/9			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0000252	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0000750	PMID:33242881	PCS		8/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0001300	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002396	PMID:33242881	PCS	HP:0003621	1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0001263	PMID:33242881	PCS		9/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0002072	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0031951	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0100660	PMID:33242881	PCS		2/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0000709	PMID:33242881	PCS	HP:0003581	1/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0000729	PMID:33242881	PCS		6/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0007018	PMID:33242881	PCS		3/10			P	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0000006	PMID:33242881	PCS					I	HPO:probinson[2022-03-05]
OMIM:619725	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities		HP:0001336	PMID:33242881	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:609536	C5 deficiency		HP:0025434	PMID:23371790	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:609536	C5 deficiency		HP:0002041	OMIM:609536	TAS					P	HPO:probinson[2013-04-01]
OMIM:609536	C5 deficiency		HP:0005430	PMID:23743184	PCS					P	HPO:probinson[2021-05-06];HPO:probinson[2022-07-10]
OMIM:609536	C5 deficiency		HP:0000007	PMID:7730648	PCS					I	HPO:probinson[2013-04-01];HPO:probinson[2020-07-22]
OMIM:609536	C5 deficiency		HP:0005381	PMID:23371790	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:609536	C5 deficiency		HP:0007569	OMIM:609536	TAS					P	HPO:probinson[2013-01-09]
OMIM:609536	C5 deficiency		HP:0033060	PMID:23371790	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:600274	Frontotemporal dementia		HP:0002476	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0001300	PMID:6524873	PCS		4/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-16]
OMIM:600274	Frontotemporal dementia		HP:0003596	PMID:6524873	IEA		9/10			C	HPO:probinson[2022-06-16]
OMIM:600274	Frontotemporal dementia		HP:0002463	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0002145	OMIM:600274	TAS					P	HPO:probinson[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0002591	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000727	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000737	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000748	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000726	PMID:6524873	PCS		7/10			P	HPO:probinson[2022-06-16]
OMIM:600274	Frontotemporal dementia		HP:0000734	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000745	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0007354	PMID:6524873	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-16]
OMIM:600274	Frontotemporal dementia		HP:0002529	OMIM:600274	TAS					P	HPO:probinson[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0025710	PMID:6524873	PCS		1/10			C	HPO:probinson[2022-06-16]
OMIM:600274	Frontotemporal dementia		HP:0000741	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000751	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000710	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0000006	OMIM:600274	IEA					I	HPO:iea[2009-02-17]
OMIM:600274	Frontotemporal dementia		HP:0008768	OMIM:600274	IEA					P	HPO:iea[2009-02-17]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001660	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0003577	PMID:26299364	PCS		23/23			C	HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001156	PMID:26299364	PCS		8/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0000089	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001362	PMID:26299364	PCS		3/23			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001395	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0002040	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0005180	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001849	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001409	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001629	PMID:26299364	PCS		2/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0007385	PMID:26299364	PCS		16/23			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0000965	PMID:26299364	PCS		2/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001800	PMID:26299364	PCS		1/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001159	PMID:26299364	PCS		4/23			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0000006	PMID:26299364	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-05]
OMIM:616589	Adams-Oliver syndrome 6		HP:0001744	PMID:26299364	PCS		1/23			P	HPO:probinson[2022-09-05]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0000473	PMID:33889951	PCS		2/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0003621	PMID:33889951	PCS		2/5			C	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0002015	PMID:33889951	PCS		4/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0000640	PMID:33889951	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0002067	PMID:33889951	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0001272	PMID:33889951	PCS		5/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0001260	PMID:33889951	PCS		5/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0002066	PMID:33889951	PCS		5/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0003474	PMID:33889951	PCS		0/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0001152	PMID:33889951	PCS		4/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0002174	PMID:33889951	PCS		2/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0002070	PMID:33889951	PCS		5/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0045084	PMID:33889951	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0011462	PMID:33889951	PCS		3/5			C	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0000508	PMID:33889951	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0000338	PMID:33889951	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0000007	PMID:33889951	PCS					I	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0007366	PMID:33889951	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0040129	PMID:33889951	PCS		0/5			P	HPO:probinson[2022-07-16]
OMIM:619862	Spinocerebellar ataxia, autosomal recessive 32		HP:0007338	PMID:33889951	PCS		4/5			P	HPO:probinson[2022-07-16]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001650	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0003774	PMID:18371931	PCS		2/2			P	HPO:probinson[2022-08-19];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001396	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0004467	PMID:18371931	PCS		1/3			P	HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0003577	PMID:18371931	PCS		2/3			C	HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0002089	OMIM:208540	TAS					P	HPO:probinson[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001696	PMID:18371931	PCS		1/3			P	HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0000083	PMID:18371931	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001395	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001394	PMID:18371931	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0002240	PMID:18371931	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0003593	PMID:18371931	PCS		1/3			C	HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001409	PMID:18371931	PCS		1/3			P	HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001408	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001746	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0006276	PMID:18371931	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001305	OMIM:208540	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001407	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001748	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001643	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0002613	PMID:18371931	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0000113	PMID:18371931	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001744	PMID:18371931	PCS		1/2			P	HPO:probinson[2022-08-19];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001562	PMID:18371931	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0000110	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0100732	OMIM:208540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0000007	PMID:18371931	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0006563	PMID:18371931	PCS		2/3			P	HPO:probinson[2022-08-19];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001737	OMIM:208540	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0002009	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0003811	PMID:18371931	PCS		1/2			C	HPO:probinson[2022-08-19]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0001631	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0000105	OMIM:208540	IEA					P	HPO:iea[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0002566	OMIM:208540	TAS					P	HPO:probinson[2009-02-17]
OMIM:208540	Renal-hepatic-pancreatic dysplasia 1		HP:0005999	OMIM:208540	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003642	PMID:19576565	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003621	PMID:19576565	PCS		1/1			C	HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003236	PMID:19576565;PMID:28803818	PCS		2/2			P	HPO:probinson[2021-06-30];HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003198	PMID:28803818	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003581	PMID:28803818	PCS		1/1			C	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003391	PMID:28803818	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003805	PMID:19576565	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0000007	PMID:19576565	PCS		1/1			I	HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0002515	PMID:19576565	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0002317	PMID:28803818	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0006785	PMID:28803818	PCS		1/1			P	HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003701	PMID:28803818	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0001324	PMID:19576565	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0002910	PMID:19576565	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0003557	PMID:19576565	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612937	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15		HP:0001644	PMID:19576565	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2021-06-30]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0002653	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0004322	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0003165	OMIM:612089	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0003072	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0007099	OMIM:612089	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0002748	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0000117	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0000843	OMIM:612089	IEA					P	HPO:skoehler[2015-01-21]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0002007	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0004912	OMIM:612089	IEA					P	HPO:skoehler[2015-01-21]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0000256	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0000006	OMIM:612089	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0000897	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0002148	OMIM:612089	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612089	Hypophosphatemic rickets and hyperparathyroidism		HP:0008208	OMIM:612089	IEA					P	HPO:skoehler[2010-06-20]
OMIM:193900	White sponge nevus 1		HP:0000502	PMID:7493030	PCS		0/8			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:193900	White sponge nevus 1		HP:0002745	PMID:7493030	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:193900	White sponge nevus 1		HP:0000006	PMID:7493030	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0012265	OMIM:610852	IEA					P	HPO:skoehler[2015-01-19]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0200109	OMIM:610852	TAS					P	HPO:skoehler[2013-06-05]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0012262	OMIM:610852	TAS					P	HPO:probinson[2013-04-07]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0000007	OMIM:610852	IEA					I	HPO:skoehler[2010-06-19]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0005938	PMID:17360648	TAS					P	HPO:probinson[2013-04-07]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0000246	OMIM:610852	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0002205	OMIM:610852	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610852	Ciliary dyskinesia, primary, 6		HP:0011108	OMIM:610852	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253550	Spinal muscular atrophy, type II		HP:0003202	OMIM:253550	IEA					P	HPO:iea[2009-02-17]
OMIM:253550	Spinal muscular atrophy, type II		HP:0002378	OMIM:253550	IEA					P	HPO:iea[2009-02-17]
OMIM:253550	Spinal muscular atrophy, type II		HP:0002398	OMIM:253550	IEA					P	HPO:iea[2009-02-17]
OMIM:253550	Spinal muscular atrophy, type II		HP:0000007	OMIM:253550	IEA					I	HPO:iea[2009-02-17]
OMIM:253550	Spinal muscular atrophy, type II		HP:0001308	OMIM:253550	IEA					P	HPO:iea[2009-02-17]
OMIM:253550	Spinal muscular atrophy, type II		HP:0007269	OMIM:253550	IEA					P	HPO:skoehler[2015-01-27]
OMIM:253550	Spinal muscular atrophy, type II		HP:0001324	OMIM:253550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253550	Spinal muscular atrophy, type II		HP:0002205	OMIM:253550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253550	Spinal muscular atrophy, type II		HP:0003457	OMIM:253550	IEA					P	HPO:iea[2009-02-17]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000970	OMIM:224900	TAS					P	HPO:skoehler[2013-10-22]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0010803	OMIM:224900	IEA					P	HPO:iea[2012-03-01]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000232	OMIM:224900	IEA					P	HPO:iea[2009-02-17]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002046	PMID:15373768	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0007607	PMID:15373768	PCS					P	HPO:skoehler[2015-01-14];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000691	PMID:15373768	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0005280	PMID:15373768	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0045075	PMID:15373768	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0008070	PMID:15373768	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0011463	PMID:15373768	PCS		1/1			C	HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0012471	OMIM:224900	TAS					P	HPO:skoehler[2014-11-26]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000607	PMID:15373768	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000668	OMIM:224900	IEA					P	HPO:iea[2009-02-17]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000007	PMID:10431241	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000966	PMID:15373768	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0002007	OMIM:224900	IEA					P	HPO:iea[2009-02-17]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000653	PMID:15373768	PCS		1/1			P	HPO:iea[2012-03-01];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000674	OMIM:224900	IEA					P	HPO:iea[2009-02-17]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0001106	PMID:15373768	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000677	PMID:15373768	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:224900	Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive		HP:0000698	PMID:15373768	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:273680	Thanatophoric dysplasia, glasgow variant		HP:0002983	OMIM:273680	IEA					P	HPO:iea[2009-02-17]
OMIM:273680	Thanatophoric dysplasia, glasgow variant		HP:0000518	OMIM:273680	IEA					P	HPO:iea[2009-02-17]
OMIM:273680	Thanatophoric dysplasia, glasgow variant		HP:0001903	OMIM:273680	IEA					P	HPO:iea[2009-02-17]
OMIM:273680	Thanatophoric dysplasia, glasgow variant		HP:0001939	OMIM:273680	IEA					P	HPO:iea[2009-02-17]
OMIM:273680	Thanatophoric dysplasia, glasgow variant		HP:0000007	OMIM:273680	IEA					I	HPO:iea[2009-02-17]
OMIM:273680	Thanatophoric dysplasia, glasgow variant		HP:0003811	OMIM:273680	IEA					C	HPO:iea[2009-02-17]
OMIM:273680	Thanatophoric dysplasia, glasgow variant		HP:0001433	OMIM:273680	IEA					P	HPO:iea[2009-02-17]
OMIM:604827	Myoclonic epilepsy, juvenile, 2		HP:0002069	OMIM:604827	TAS					P	HPO:probinson[2009-02-17]
OMIM:604827	Myoclonic epilepsy, juvenile, 2		HP:0000007	OMIM:604827	IEA					I	HPO:iea[2009-02-17]
OMIM:604827	Myoclonic epilepsy, juvenile, 2		HP:0001336	OMIM:604827	TAS					P	HPO:probinson[2012-07-16]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0005575	PMID:15173250	PCS		3/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-11-07]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0005421	PMID:15173250	PCS		2/3			P	HPO:probinson[2022-11-07]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0000790	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0000093	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0001919	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0001937	PMID:15173250	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-07]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0001903	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0011463	PMID:15173250	PCS		1/3			C	HPO:probinson[2022-11-07]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0011462	PMID:15173250	PCS		2/3			C	HPO:probinson[2022-11-07]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0000822	OMIM:612923	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0100519	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0001873	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0000006	PMID:15173250	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-07]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0003259	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612923	Hemolytic uremic syndrome, atypical, susceptibility to, 3		HP:0003138	OMIM:612923	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0000286	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001254	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001651	PMID:19136951	PCS		1/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0004322	PMID:19136951	PCS		3/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001252	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003153	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003593	PMID:19136951	PCS		7/12			C	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0002240	PMID:19136951	PCS		2/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001290	OMIM:277380	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0002160	PMID:19136951	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0033443	PMID:19136951	PCS		3/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001508	PMID:19136951	PCS		6/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0002719	PMID:19136951	PCS		1/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0011463	PMID:19136951	PCS		1/12			C	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001903	PMID:19136951	PCS		3/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0008551	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001889	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0000219	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0000218	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0002912	PMID:19136951	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001643	PMID:19136951	PCS		1/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003524	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003623	PMID:19136951	PCS		3/12			C	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0002311	OMIM:277380	TAS					P	HPO:skoehler[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0002575	PMID:19136951	PCS		1/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003621	PMID:19136951	PCS		1/12			C	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003145	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001762	PMID:19136951	PCS		1/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003223	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0002156	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0003286	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0011968	PMID:19136951	PCS		4/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001263	PMID:19136951	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0010280	PMID:19136951	PCS		4/12			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001518	PMID:19136951	PCS		4/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0012120	PMID:19136951	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0000206	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0000007	PMID:19136951	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0000988	PMID:19136951	PCS		1/12			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001873	PMID:19136951	PCS		1/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001631	PMID:19136951	PCS		1/12			P	HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0000369	OMIM:277380	IEA					P	HPO:iea[2009-02-17]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001876	PMID:19136951	PCS		1/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:277380	Methylmalonic aciduria and homocystinuria, Cblf type		HP:0001875	PMID:19136951	PCS		2/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000486	PMID:35121750	PCS		4/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000463	PMID:35121750	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001250	PMID:35121750	PCS		7/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001252	PMID:35121750	PCS		5/8			P	HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0002020	PMID:35121750	PCS		3/7			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0003593	PMID:35121750	PCS		6/8			C	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001270	PMID:35121750	PCS		4/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0002181	PMID:35121750	PCS		1/5			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000639	PMID:35121750	PCS		5/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0002719	PMID:35121750	PCS		4/7			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001508	PMID:35121750	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0100704	PMID:35121750	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0011461	PMID:35121750	PCS		2/8			C	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000218	PMID:35121750	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000158	PMID:35121750	PCS		1/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001249	PMID:35121750	PCS		8/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001320	PMID:35121750	PCS		1/5			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0002059	PMID:35121750	PCS		2/5			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000252	PMID:35121750	PCS		7/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000276	PMID:35121750	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0011968	PMID:35121750	PCS		3/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001263	PMID:35121750	PCS					P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0100021	PMID:35121750	PCS		3/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0007371	PMID:35121750	PCS		2/5			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0007178	PMID:35121750	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000007	PMID:35121750	PCS					I	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001558	PMID:35121750	PCS		2/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0000648	PMID:35121750	PCS		1/8			P	HPO:probinson[2022-07-20]
OMIM:619876	Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures		HP:0001257	PMID:35121750	PCS		3/8			P	HPO:probinson[2022-07-20]
OMIM:302045	Cardiomyopathy, dilated, 3B		HP:0003621	PMID:8361506	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:302045	Cardiomyopathy, dilated, 3B		HP:0032232	PMID:8361506	PCS		4/4			P	HPO:probinson[2022-07-04]
OMIM:302045	Cardiomyopathy, dilated, 3B		HP:0001417	PMID:8361506	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-04]
OMIM:302045	Cardiomyopathy, dilated, 3B		HP:0033755	PMID:8361506	PCS		4/4			P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:302045	Cardiomyopathy, dilated, 3B		HP:0001644	PMID:8361506	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-04]
OMIM:302045	Cardiomyopathy, dilated, 3B		HP:0003557	PMID:8361506	PCS					P	HPO:probinson[2022-07-04]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0002059	OMIM:617873	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0000252	PMID:24901367	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0001344	OMIM:617873	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0002353	PMID:24901367	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0000750	PMID:24901367	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0001332	OMIM:617873	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0002123	PMID:24901367	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0031936	PMID:24901367	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0002373	PMID:24901367	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0001263	PMID:24901367	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0003593	PMID:24901367	PCS		1/1			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0001290	OMIM:617873	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0011923	PMID:24901367	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0001508	OMIM:617873	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0000007	PMID:24901367	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0200134	PMID:24901367	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0008347	PMID:24901367	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0000565	OMIM:617873	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0007766	OMIM:617873	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0001257	PMID:24901367	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0001249	OMIM:617873	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617873	Combined oxidative phosphorylation deficiency 35		HP:0000545	OMIM:617873	IEA					P	HPO:skoehler[2018-10-08]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0000473	PMID:31636353	PCS		1/9		HP:0012825	P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0003477	PMID:31636353	PCS		2/7			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0002015	PMID:31636353	PCS		2/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0003487	PMID:31636353	PCS		8/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0001272	PMID:31636353	PCS		2/7			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0001260	PMID:31636353	PCS		6/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0002495	PMID:31636353	PCS		1/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0010829	PMID:31636353	PCS		1/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0000020	PMID:31636353	PCS		2/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0001152	PMID:31636353	PCS		4/4			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0002061	PMID:31636353	PCS		9/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0010830	PMID:31636353	PCS		1/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0001270	PMID:31636353	PCS		5/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0010831	PMID:31636353	PCS		0/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0011463	PMID:31636353	PCS		9/9			C	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0007340	PMID:31636353	PCS		7/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0000007	PMID:31636353	PCS					I	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0000648	PMID:31636353	PCS		7/7			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0001258	PMID:31636353	PCS					P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0006986	PMID:31636353	PCS		4/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0001348	PMID:31636353	PCS		9/9			P	HPO:probinson[2022-03-25]
OMIM:619686	Spastic paraplegia 85, autosomal recessive		HP:0003700	PMID:31636353	PCS		1/9			P	HPO:probinson[2022-03-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0002267	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001276	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0008936	PMID:31314961;PMID:31332433	PCS		2/2			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0002411	PMID:31314961	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001561	PMID:31332433	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001344	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0003487	PMID:31314961;PMID:31332433	PCS		2/2			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001272	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0002151	PMID:31314961	IEA		1/1			P	HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001285	PMID:31314961	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001251	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0003593	PMID:31332433	PCS		1/1			C	HPO:probinson[2022-08-27]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0002380	PMID:31314961;PMID:31332433	PCS		1/2			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25];HPO:probinson[2020-07-25];HPO:probinson[2020-07-25];HPO:probinson[2022-09-04]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0002061	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0011448	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001845	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0007256	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0000007	PMID:31314961	PCS					I	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0000369	PMID:31332433	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0000358	PMID:31332433	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:618598	Spastic tetraplegia and axial hypotonia, progressive		HP:0001347	PMID:31332433	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0000253	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0001265	PMID:35948005	PCS		10/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0008936	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0002411	PMID:35948005	PCS		5/8			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0001385	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0002375	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0004322	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0000160	PMID:35948005	PCS		6/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0001263	PMID:35948005	PCS		16/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0001251	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0003593	PMID:35948005	PCS		8/16			C	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0012389	PMID:35948005	PCS		3/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0001508	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0002808	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0011463	PMID:35948005	PCS		8/16			C	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0000739	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0000007	PMID:35948005	PCS					I	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0000964	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0001308	PMID:35948005	PCS		3/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0000317	PMID:35948005	PCS		7/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0000768	PMID:35948005	PCS		1/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0007018	PMID:35948005	PCS		4/16			P	HPO:probinson[2022-08-28]
OMIM:620007	Intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects		HP:0001249	PMID:35948005	PCS		13/13			P	HPO:probinson[2022-08-28]
OMIM:300652	Angioma serpiginosum, X-linked		HP:0003577	OMIM:300652	IEA					C	HPO:iea[2009-02-17]
OMIM:300652	Angioma serpiginosum, X-linked		HP:0002213	OMIM:300652	PCS					P	HPO:iea[2012-03-01]
OMIM:300652	Angioma serpiginosum, X-linked		HP:0001423	OMIM:300652	IEA					I	HPO:iea[2009-02-17]
OMIM:300652	Angioma serpiginosum, X-linked		HP:0008404	OMIM:300652	TAS					P	HPO:probinson[2013-04-01]
OMIM:300652	Angioma serpiginosum, X-linked		HP:0008070	OMIM:300652	TAS					P	HPO:probinson[2009-02-17]
OMIM:300652	Angioma serpiginosum, X-linked		HP:0003677	OMIM:300652	IEA					C	HPO:iea[2009-02-17]
OMIM:300652	Angioma serpiginosum, X-linked		HP:0000962	OMIM:300652	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0001177	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0003015	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0004322	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0001156	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:252100	Mohr syndrome		HP:0000161	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000180	ISBN-13:978-0721606156;OMIM:252100	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0010101	OMIM:252100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:252100	Mohr syndrome		HP:0010297	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:252100	Mohr syndrome		HP:0000316	OMIM:252100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:252100	Mohr syndrome		HP:0000238	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000218	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0006136	OMIM:252100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:252100	Mohr syndrome		HP:0000455	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0001841	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:252100	Mohr syndrome		HP:0000456	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000175	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0002650	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0004279	OMIM:252100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:252100	Mohr syndrome		HP:0000199	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0003025	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0001162	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:252100	Mohr syndrome		HP:0002132	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000272	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000191	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:252100	Mohr syndrome		HP:0005280	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000506	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000327	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000767	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000007	ISBN-13:978-0721606156	PCS					I	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0006289	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0000405	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0004209	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:252100	Mohr syndrome		HP:0001159	OMIM:252100	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0002645	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:252100	Mohr syndrome		HP:0001830	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:252100	Mohr syndrome		HP:0000347	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:601977	Thrombocythemia 2		HP:0005513	PMID:14764528	PCS					P	HPO:probinson[2019-07-13]
OMIM:601977	Thrombocythemia 2		HP:0001894	PMID:14764528	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-07-13]
OMIM:601977	Thrombocythemia 2		HP:0001442	PMID:16868251	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-13]
OMIM:601977	Thrombocythemia 2		HP:0000006	PMID:14764528	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-07-13]
OMIM:165700	Thiemann disease		HP:0006009	OMIM:165700	TAS					P	HPO:iea[2012-07-22]
OMIM:165700	Thiemann disease		HP:0010885	OMIM:165700	IEA					P	HPO:skoehler[2019-09-07]
OMIM:165700	Thiemann disease		HP:0000006	OMIM:165700	IEA					I	HPO:iea[2009-02-17]
OMIM:165700	Thiemann disease		HP:0009803	OMIM:165700	TAS					P	HPO:iea[2012-07-22]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0003621	PMID:24777450	PCS		4/10			C	HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0003596	PMID:24777450	PCS		1/10			C	HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0011463	PMID:24777450	PCS		3/10			C	HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0011462	PMID:24777450	PCS		2/10			C	HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0001635	PMID:24777450	PCS		10/10			P	HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0004308	PMID:24777450	PCS		5/10			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0012664	PMID:24777450	PCS		10/10			P	HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0001653	PMID:24777450	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0033755	PMID:24777450	PCS		8/10			P	HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0000006	PMID:24777450	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0001644	PMID:24777450	PCS		10/10			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-07-03]
OMIM:615916	Cardiomyopathy, dilated, 1nn		HP:0012249	PMID:24777450	PCS		9/10			P	HPO:probinson[2022-07-03]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0005656	PMID:36943452	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000286	PMID:37163662;PMID:36943452	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0010648	PMID:36943452	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0004322	PMID:36943452	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001250	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000160	PMID:37163662	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001252	PMID:37163662;PMID:36943452	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0003273	PMID:37163662;PMID:36943452	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0011816	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0410030	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0003391	PMID:37163662	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000954	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000316	PMID:37163662	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000873	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0003306	PMID:37163662	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001249	PMID:37163662	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000252	PMID:37163662;PMID:36943452	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000494	PMID:37163662;PMID:36943452	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000175	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000054	PMID:37163662	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001382	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001263	PMID:37163662;PMID:36943452	PCS		7/10			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000294	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0034665	PMID:36943452	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0100021	PMID:37163662;PMID:36943452	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001181	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0010557	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0012385	PMID:36943452	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0034671	PMID:37163662;PMID:36943452	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000448	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000767	PMID:36943452	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0002507	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000007	PMID:36943452	PCS					I	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0008800	PMID:36943452	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0034391	PMID:37163662;PMID:36943452	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000325	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0003577	PMID:37163662;PMID:36943452	PCS		10/10			C	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000343	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000463	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0002000	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0003691	PMID:37163662;PMID:36943452	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001270	PMID:37163662;PMID:36943452	PCS		7/10			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0010501	PMID:36943452	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001629	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000218	PMID:37163662;PMID:36943452	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0002996	PMID:36943452	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001562	PMID:37163662	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0002650	PMID:37163662;PMID:36943452	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001762	PMID:37163662;PMID:36943452	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000750	PMID:37163662;PMID:36943452	PCS		8/10			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000475	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000431	PMID:37163662	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000276	PMID:36943452	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001684	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000193	PMID:36943452	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000470	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0005280	PMID:37163662	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0008180	PMID:37163662	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001838	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0002808	PMID:37163662;PMID:36943452	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000508	PMID:37163662	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0003738	PMID:37163662	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001239	PMID:36943452	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001558	PMID:36943452	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000505	PMID:37163662	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0001159	PMID:36943452	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000465	PMID:37163662;PMID:36943452	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000347	PMID:36943452	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:620775	Neuromuscular disorder, congenital, with dysmorphic facies		HP:0000028	PMID:37163662	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-09-22]
OMIM:128600	Ear malformation		HP:0000598	OMIM:128600	IEA					P	HPO:iea[2009-02-17]
OMIM:128600	Ear malformation		HP:0000006	OMIM:128600	IEA					I	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000563	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0001377	PMID:12624132	PCS		167/240			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0000100	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0004322	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0005255	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000083	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0001032	PMID:12624132	PCS		114/119			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0000482	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0009780	PMID:12624132	PCS		34/50			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0012376	OMIM:161200	TAS					P	HPO:skoehler[2013-10-22]
OMIM:161200	Nail-Patella syndrome		HP:0009760	PMID:12624132	PCS		15/123			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0000518	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0009781	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0001807	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0009783	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0002938	PMID:12624132	PCS		41/87			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0006650	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0009785	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0002999	PMID:12624132	PCS		30/118			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0009788	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0002414	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0006633	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0001763	PMID:12624132	PCS		76/118			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0006437	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0006657	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000099	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000175	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0002650	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0001762	PMID:12624132	PCS		23/122			P	HPO:iea[2009-02-17];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0000790	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0003065	PMID:12624132	PCS		179/237			P	HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0000093	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000407	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000508	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000767	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0006443	PMID:12624132	PCS		21/237			P	HPO:skoehler[2010-06-20];HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0004209	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0003418	PMID:12624132	PCS		66/120			P	HPO:probinson[2019-05-09]
OMIM:161200	Nail-Patella syndrome		HP:0001598	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0006424	OMIM:161200	TAS					P	HPO:probinson[2013-04-14]
OMIM:161200	Nail-Patella syndrome		HP:0000006	OMIM:161200	IEA					I	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000204	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0000501	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0001798	OMIM:161200	IEA					P	HPO:iea[2009-02-17]
OMIM:161200	Nail-Patella syndrome		HP:0003997	OMIM:161200	TAS					P	HPO:probinson[2013-04-14]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0000286	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0001156	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0001382	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0001263	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0001251	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0003593	PMID:33909043	PCS		1/1			C	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0045055	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0045075	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0008070	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0008064	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0032152	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0000007	PMID:33909043	PCS					I	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0000689	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0002705	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0008404	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0001249	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:619692	Trichothiodystrophy 9, nonphotosensitive		HP:0001315	PMID:33909043	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001265	PMID:23857908	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0003621	PMID:23857908	PCS		4/4			C	HPO:probinson[2022-10-22];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001761	OMIM:615043	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001288	PMID:23857908	PCS	HP:0003621	4/4			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0003487	OMIM:615043	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0003693	PMID:23857908	PCS		3/4			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001260	OMIM:615043	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0006380	OMIM:615043	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0009830	PMID:23857908	PCS		4/4			P	HPO:probinson[2022-10-22];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0002936	PMID:23857908	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0000007	PMID:23857908	PCS					I	HPO:skoehler[2013-02-25];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0000648	PMID:23857908	PCS		2/4			P	HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0006466	OMIM:615043	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0002505	PMID:23857908	PCS	HP:0025710	2/2			P	HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001258	PMID:23857908	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001324	PMID:23857908	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001257	PMID:23857908	PCS	HP:0003621	4/4			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0003677	PMID:23857908	PCS					C	HPO:skoehler[2013-02-25];HPO:probinson[2022-10-22]
OMIM:615043	Spastic paraplegia 43, autosomal recessive		HP:0001347	OMIM:615043	TAS					P	HPO:skoehler[2013-02-25]
OMIM:617654	Deafness, autosomal recessive 108		HP:0003593	OMIM:617654	IEA					C	HPO:skoehler[2019-09-07]
OMIM:617654	Deafness, autosomal recessive 108		HP:0000007	PMID:27162350	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2019-06-13]
OMIM:617654	Deafness, autosomal recessive 108		HP:0000612	PMID:27162350	PCS		1/2		HP:0012833	P	HPO:probinson[2019-06-13]
OMIM:617654	Deafness, autosomal recessive 108		HP:0001270	PMID:27162350	PCS		0/2			P	HPO:probinson[2019-06-13];HPO:probinson[2024-03-15]
OMIM:617654	Deafness, autosomal recessive 108		HP:0008527	PMID:27162350	PCS	HP:0003577	2/2		HP:0012829	P	HPO:probinson[2019-06-13]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0002059	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0002133	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0001399	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0001250	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0003572	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0001272	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0001285	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0001263	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0002072	PMID:28973171	PCS	HP:0003593	1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0012847	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0011923	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0100660	PMID:28973171	PCS	HP:0003593	1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0100248	PMID:28973171	PCS	HP:0003593	1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0003819	PMID:28973171	PCS		1/1			C	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0001987	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0000007	PMID:28973171	PCS					I	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0008347	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618567	Mitochondrial DNA depletion syndrome 17		HP:0001941	PMID:28973171	PCS		1/1			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0003676	PMID:21330303	PCS					C	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0000486	OMIM:611225	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0002540	PMID:21330303	PCS		11/11			P	HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0001250	OMIM:611225	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0003593	PMID:21330303	PCS					C	HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0002061	OMIM:611225	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0033205	PMID:21330303	PCS		4/4			P	HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0011463	PMID:21330303	PCS					C	HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0007340	OMIM:611225	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0000218	OMIM:611225	TAS					P	HPO:skoehler[2014-02-25]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0001249	OMIM:611225	IEA		11/11			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0001347	OMIM:611225	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0003202	OMIM:611225	TAS					P	HPO:skoehler[2014-02-25]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0001344	PMID:21330303	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0002650	OMIM:611225	TAS					P	HPO:skoehler[2014-02-25]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0003487	PMID:21330303	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0031936	PMID:21330303	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0001288	OMIM:611225	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0002079	OMIM:611225	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0001761	OMIM:611225	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0011448	PMID:21330303	PCS		2/4			P	HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0034392	PMID:21330303	PCS		11/11			P	HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0002808	OMIM:611225	TAS					P	HPO:skoehler[2014-02-25]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0000007	PMID:21330303	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0001258	PMID:21330303	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-04-08]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0003677	OMIM:611225	TAS					C	HPO:skoehler[2012-10-17]
OMIM:611225	Spastic paraplegia 18, autosomal recessive		HP:0006986	OMIM:611225	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182170	Anemia, sideroblastic, autosomal dominant		HP:0004828	PMID:3653362	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:182170	Anemia, sideroblastic, autosomal dominant		HP:0001877	PMID:3653362	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:182170	Anemia, sideroblastic, autosomal dominant		HP:0001924	PMID:26491070	PCS					P	HPO:iea[2009-02-17]
OMIM:182170	Anemia, sideroblastic, autosomal dominant		HP:0000006	PMID:26491070	PCS					I	HPO:iea[2009-02-17]
OMIM:611543	Cavitary optic disc anomalies		HP:0000662	OMIM:611543	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:611543	Cavitary optic disc anomalies		HP:0500087	OMIM:611543	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:611543	Cavitary optic disc anomalies		HP:0001123	OMIM:611543	TAS					P	HPO:skoehler[2015-12-30]
OMIM:611543	Cavitary optic disc anomalies		HP:0007663	OMIM:611543	TAS					P	HPO:skoehler[2015-12-30]
OMIM:611543	Cavitary optic disc anomalies		HP:0000006	OMIM:611543	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0003577	PMID:27545674	PCS		1/9			C	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0002188	PMID:27545674	PCS		3/7			P	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0001332	PMID:27545674	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0004322	PMID:27545674	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0001272	PMID:27545674	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0001250	PMID:27545674	PCS		8/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0002020	PMID:27545674	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0003593	PMID:27545674	PCS		3/9			C	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0012469	PMID:27545674	PCS		4/9			P	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0001508	OMIM:617132	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0000737	PMID:27545674	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0000817	PMID:27545674	PCS		4/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0003623	PMID:27545674	PCS		5/9			C	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0008936	PMID:27545674	PCS		9/9			P	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0002059	PMID:27545674	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0001344	PMID:27545674	PCS		8/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0002079	OMIM:617132	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0000298	OMIM:617132	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0011968	OMIM:617132	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0001263	PMID:27545674	PCS		9/9			P	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0005484	PMID:27545674	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0000007	PMID:27545674	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0200134	PMID:27545674	PCS		9/9			P	HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0002305	PMID:27545674	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617132	Developmental and epileptic encephalopathy 44		HP:0001257	PMID:27545674	PCS		8/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0001298	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0002267	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0002169	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0000252	OMIM:618201	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0003676	OMIM:618201	IEA					C	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0002133	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0002376	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0002120	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0001371	OMIM:618201	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0002098	OMIM:618201	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0001263	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0010546	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0001508	OMIM:618201	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0000007	PMID:28364549	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-05-20]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0001257	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0001347	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618201	Epileptic encephalopathy, early infantile, 68		HP:0001336	OMIM:618201	IEA					P	HPO:skoehler[2019-02-15]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0003642	PMID:11134235	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0008936	OMIM:603147	IEA					P	HPO:iea[2009-02-17]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0003621	PMID:11134235	PCS		1/1			C	HPO:probinson[2022-05-07]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0000486	OMIM:603147	IEA					P	HPO:iea[2009-02-17]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0001250	PMID:11134235	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0001263	OMIM:603147;PMID:11134235	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07];HPO:skoehler[2019-02-22]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0001252	PMID:11134235	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0001251	OMIM:603147	IEA					P	HPO:iea[2009-02-17]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0001284	PMID:11134235	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0008150	OMIM:603147	IEA					P	HPO:iea[2009-02-17]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0001929	OMIM:603147	IEA					P	HPO:iea[2009-02-17]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0000007	OMIM:603147	IEA					I	HPO:iea[2009-02-17]
OMIM:603147	Congenital disorder of glycosylation, type Ic		HP:0001976	OMIM:603147	IEA					P	HPO:iea[2009-02-17]
OMIM:615725	Retinitis pigmentosa 68		HP:0007737	PMID:24670872	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:615725	Retinitis pigmentosa 68		HP:0000662	PMID:24670872	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-23]
OMIM:615725	Retinitis pigmentosa 68		HP:0001123	PMID:24670872	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-23]
OMIM:615725	Retinitis pigmentosa 68		HP:0011463	PMID:24670872	PCS		1/1			C	HPO:probinson[2023-03-23]
OMIM:615725	Retinitis pigmentosa 68		HP:0000007	PMID:24670872	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-23]
OMIM:615725	Retinitis pigmentosa 68		HP:0007663	PMID:24670872	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:615725	Retinitis pigmentosa 68		HP:0000510	PMID:24670872	PCS		1/1			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-03-23]
OMIM:615725	Retinitis pigmentosa 68		HP:0001105	PMID:24670872	PCS		1/1			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-03-23]
OMIM:142340	Diaphragmatic hernia, congenital		HP:0001426	OMIM:142340	IEA					I	HPO:iea[2009-02-17]
OMIM:142340	Diaphragmatic hernia, congenital		HP:0000776	OMIM:142340	IEA					P	HPO:iea[2009-02-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0000121	PMID:9643991	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0003159	PMID:9643991	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0025324	OMIM:259900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0000083	PMID:9643991	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0025520	OMIM:259900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0003593	PMID:9643991	PCS		1/1			C	HPO:probinson[2022-08-16]
OMIM:259900	Hyperoxaluria, primary, type I		HP:6000431	PMID:4701948	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0035005	PMID:2880111	PCS					P	HPO:probinson[2024-01-06]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0011001	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0008672	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0001944	PMID:9643991	PCS		1/1			P	HPO:probinson[2022-08-16]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0004417	OMIM:259900	IEA					P	HPO:iea[2009-02-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0002756	OMIM:259900	IEA					P	HPO:iea[2009-02-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0001942	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0002653	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0004950	OMIM:259900	IEA					P	HPO:iea[2009-02-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0011506	OMIM:259900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0001063	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0000790	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0030880	OMIM:259900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0030507	PMID:23666469	PCS					P	HPO:probinson[2015-08-05]
OMIM:259900	Hyperoxaluria, primary, type I		HP:6000702	PMID:449695	PCS		2/2			P	HPO:probinson[2024-05-09]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0100758	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0009830	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0000965	OMIM:259900	IEA					P	HPO:iea[2009-02-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0000007	PMID:2039493	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0000648	OMIM:259900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0000488	OMIM:259900	TAS					P	HPO:skoehler[2015-07-26]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0001678	OMIM:259900	TAS					P	HPO:probinson[2012-04-11]
OMIM:259900	Hyperoxaluria, primary, type I		HP:0001138	OMIM:259900	IEA					P	HPO:iea[2009-02-17]
OMIM:615731	Nemaline myopathy 9		HP:0000175	PMID:24268659	PCS		1/5			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0001561	PMID:24268659	PCS		1/4			P	HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0002650	PMID:24268659	PCS		1/5			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0001270	OMIM:615731	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615731	Nemaline myopathy 9		HP:0002093	OMIM:615731	TAS		HP:0040283			P	HPO:skoehler[2014-04-13]
OMIM:615731	Nemaline myopathy 9		HP:0001629	PMID:24268659	PCS		1/5			P	HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0002804	PMID:24268659	PCS		1/5			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0000007	PMID:24268659	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0001989	OMIM:615731	TAS		HP:0040283			P	HPO:skoehler[2014-04-13]
OMIM:615731	Nemaline myopathy 9		HP:0000218	PMID:24268659	PCS		1/5			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0001324	PMID:24268659	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0000774	PMID:24268659	PCS		1/5			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0001623	PMID:24268659	PCS		2/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0000347	PMID:24268659	PCS		1/5			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-20]
OMIM:615731	Nemaline myopathy 9		HP:0003798	PMID:24268659	PCS					P	HPO:probinson[2023-01-20]
OMIM:214800	Charge syndrome		HP:0002025	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000044	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0030732	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0002023	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000321	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000089	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000480	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000085	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0010443	PMID:17937444	PCS		1/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0011381	PMID:17937444	PCS		1/2			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000518	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0002937	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0011461	PMID:17937444	PCS		1/3			C	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0008213	OMIM:214800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214800	Charge syndrome		HP:0000316	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001888	OMIM:214800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214800	Charge syndrome		HP:0008897	PMID:15300250	PCS		19/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0002139	PMID:2260555	PCS		11/144			P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001643	PMID:17937444	PCS		1/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0003745	OMIM:214800	IEA					I	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0200021	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001642	PMID:17937444	PCS		1/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0001249	PMID:2260555	PCS		47/47			P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0003048	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000175	PMID:17937444	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000494	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000252	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000054	PMID:17937444	PCS	HP:0003577	2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000772	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000453	PMID:2260555;PMID:15300250;PMID:17937444	PCS		34/69			P	HPO:iea[2018-03-13];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0004058	PMID:17937444	PCS	HP:0003577	1/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0002032	OMIM:214800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214800	Charge syndrome		HP:0011968	OMIM:214800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214800	Charge syndrome		HP:0000050	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001263	PMID:17937444	PCS		2/2			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0003241	PMID:15300250;PMID:17937444	PCS		11/22			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0010515	OMIM:214800	TAS					P	HPO:skoehler[2013-06-05]
OMIM:214800	Charge syndrome		HP:0000528	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000407	PMID:17937444	PCS		2/2			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0012020	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0001537	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000568	OMIM:214800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214800	Charge syndrome		HP:0001539	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0002901	OMIM:214800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214800	Charge syndrome		HP:0002623	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0009778	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001018	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000006	PMID:15300250	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000204	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000369	PMID:17937444	PCS		2/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000324	PMID:16400610	PCS		36/56			P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000126	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001776	PMID:17937444	PCS		2/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000066	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0010628	PMID:15300250	PCS		5/19			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0003577	PMID:17937444	PCS		2/3			C	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000860	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001270	PMID:17937444	PCS		1/1			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0011480	PMID:17937444	PCS		2/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0001629	PMID:17937444	PCS		3/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0008551	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000458	OMIM:214800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214800	Charge syndrome		HP:0000612	PMID:9556299	PCS		79%			P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0004935	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000378	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000410	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0002575	PMID:16400610	PCS		10/55			P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0002015	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001561	PMID:17937444	PCS	HP:0011461	1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0002650	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001684	PMID:17937444	PCS	HP:0003577	1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0001360	PMID:2260555	PCS		2/144			P	HPO:iea[2018-03-13]
OMIM:214800	Charge syndrome		HP:0003022	PMID:17937444	PCS		1/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0001161	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000394	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000272	OMIM:214800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214800	Charge syndrome		HP:0000829	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0001719	PMID:17937444	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000508	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0001636	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000821	OMIM:214800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214800	Charge syndrome		HP:0000824	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000823	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0009556	PMID:17937444	PCS		2/3			P	HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0001631	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000465	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0003974	OMIM:214800	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:214800	Charge syndrome		HP:0000589	PMID:2260555;PMID:15300250;PMID:17937444	PCS		53/69			P	HPO:probinson[2012-07-16];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0000028	PMID:17937444	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-17]
OMIM:214800	Charge syndrome		HP:0002247	OMIM:214800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214800	Charge syndrome		HP:0000347	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000104	OMIM:214800	IEA					P	HPO:iea[2009-02-17]
OMIM:214800	Charge syndrome		HP:0000742	PMID:17937444	PCS		1/3			P	HPO:probinson[2022-01-17]
OMIM:263450	Polydactyly, postaxial, type A5		HP:0001162	OMIM:263450	IEA					P	HPO:iea[2009-02-17]
OMIM:263450	Polydactyly, postaxial, type A5		HP:0000007	OMIM:263450	IEA					I	HPO:iea[2009-02-17]
OMIM:263450	Polydactyly, postaxial, type A5		HP:0010554	OMIM:263450	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:263450	Polydactyly, postaxial, type A5		HP:0001159	OMIM:263450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:263450	Polydactyly, postaxial, type A5		HP:0009701	OMIM:263450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:617126	Alazami-Yuan syndrome		HP:0002465	OMIM:617126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617126	Alazami-Yuan syndrome		HP:0000343	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0004322	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000160	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0010055	PMID:25574841	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000954	PMID:25574841	PCS		1/4			P	HPO:probinson[2022-11-27];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000678	OMIM:617126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617126	Alazami-Yuan syndrome		HP:0000219	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000218	OMIM:617126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617126	Alazami-Yuan syndrome		HP:0009765	PMID:25574841	PCS		3/4			P	HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000752	OMIM:617126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617126	Alazami-Yuan syndrome		HP:0001007	PMID:25574841	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0001249	PMID:25574841	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0002553	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000252	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000574	PMID:25574841	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000430	OMIM:617126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617126	Alazami-Yuan syndrome		HP:0001263	PMID:25574841;PMID:25558065	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000294	PMID:25574841	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000426	OMIM:617126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617126	Alazami-Yuan syndrome		HP:0000448	PMID:25574841	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000007	PMID:25558065	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000527	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0001319	OMIM:617126	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617126	Alazami-Yuan syndrome		HP:0000664	PMID:25574841	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617126	Alazami-Yuan syndrome		HP:0000028	PMID:25574841	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:606995	Senior-Loken syndrome 3		HP:0000550	OMIM:606995	IEA					P	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0000572	OMIM:606995	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606995	Senior-Loken syndrome 3		HP:0003774	OMIM:606995	IEA					P	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0000639	OMIM:606995	IEA					P	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0001959	OMIM:606995	IEA					P	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0000805	OMIM:606995	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606995	Senior-Loken syndrome 3		HP:0000007	OMIM:606995	IEA					I	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0000090	OMIM:606995	IEA					P	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0000108	OMIM:606995	IEA					P	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0000103	OMIM:606995	IEA					P	HPO:iea[2009-02-17]
OMIM:606995	Senior-Loken syndrome 3		HP:0007875	OMIM:606995	IEA					P	HPO:skoehler[2010-06-20]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0001254	PMID:28419241	PCS					P	HPO:probinson[2020-07-10]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0002750	PMID:28419241	PCS					P	HPO:probinson[2020-07-10]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0031507	PMID:28419241	PCS					P	HPO:probinson[2020-07-10]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0004322	PMID:28419241	PCS					P	HPO:probinson[2020-07-10]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0000007	PMID:28419241	PCS					I	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0012378	PMID:28419241	PCS					P	HPO:probinson[2020-07-10]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0001510	PMID:28419241	PCS					P	HPO:probinson[2020-07-10]
OMIM:618573	Hypothyroidism, congenital, nongoitrous, 7		HP:0033082	PMID:28419241	PCS					P	HPO:probinson[2020-08-13]
OMIM:607453	Deafness, autosomal dominant 44		HP:0003621	PMID:17503326	PCS		18/18			C	HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:607453	Deafness, autosomal dominant 44		HP:0001751	PMID:17503326	PCS		0/18			P	HPO:lccarmody[2018-06-13];HPO:probinson[2024-03-13]
OMIM:607453	Deafness, autosomal dominant 44		HP:0000407	PMID:17503326	PCS	HP:0003621	18/18			P	HPO:probinson[2013-02-26];HPO:probinson[2024-03-13]
OMIM:607453	Deafness, autosomal dominant 44		HP:0000360	PMID:17503326	PCS		0/18			P	HPO:lccarmody[2018-06-13];HPO:probinson[2024-03-13]
OMIM:607453	Deafness, autosomal dominant 44		HP:0011390	PMID:17503326	PCS		0/1			P	HPO:probinson[2024-03-13]
OMIM:607453	Deafness, autosomal dominant 44		HP:0000006	PMID:17503326	PCS					I	HPO:probinson[2013-01-09]
OMIM:617898	Multiple synostoses syndrome 4		HP:0000362	OMIM:617898	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617898	Multiple synostoses syndrome 4		HP:0001156	OMIM:617898	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617898	Multiple synostoses syndrome 4		HP:0001845	OMIM:617898	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617898	Multiple synostoses syndrome 4		HP:0001769	OMIM:617898	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617898	Multiple synostoses syndrome 4		HP:0008368	OMIM:617898	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617898	Multiple synostoses syndrome 4		HP:0001763	OMIM:617898	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617898	Multiple synostoses syndrome 4		HP:0000006	OMIM:617898	IEA					I	HPO:skoehler[2019-04-18]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0002850	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0002465	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0002650	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0002057	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0001272	OMIM:300861	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0001250	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0001263	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0001251	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0001419	OMIM:300861	TAS					I	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0002808	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0000316	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0009830	OMIM:300861	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0000954	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0002317	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0000411	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0000664	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0000303	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0002720	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0001007	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300861	Intellectual developmental disorder, X-linked syndromic, Chudley-Schwartz type		HP:0004315	OMIM:300861	TAS					P	HPO:skoehler[2012-10-14]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0003621	PMID:35209905;PMID:11106718	PCS		7/42			C	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0031329	PMID:11106718	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0004971	OMIM:613426	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0001195	PMID:35209905	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0003581	PMID:35209905;PMID:11106718	PCS		31/42			C	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0001680	OMIM:613426	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0030682	PMID:35209905	PCS		21/23			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0003593	PMID:11106718	PCS		1/23			C	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0002092	PMID:35209905	PCS		1/19			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0012664	PMID:11106718	PCS		17/21			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0010316	PMID:35209905	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0005180	PMID:35209905	PCS		3/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0011463	PMID:35209905;PMID:11106718	PCS		3/42			C	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0011682	PMID:35209905	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0001647	OMIM:613426	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0001635	PMID:35209905;PMID:11106718	PCS		16/42			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0004308	PMID:35209905	PCS		0/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0001653	PMID:11106718	PCS		2/23			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0000006	PMID:11106718	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0001645	PMID:11106718	PCS		6/23			P	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0004756	PMID:35209905	PCS		2/19			P	HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0001644	PMID:11106718	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-15]
OMIM:613426	Cardiomyopathy, dilated, 1S		HP:0034192	PMID:18506004	PCS		2/19			P	HPO:probinson[2022-04-15]
OMIM:262000	Bjornstad syndrome		HP:0000970	PMID:17314340	PCS		5/5			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-03-20]
OMIM:262000	Bjornstad syndrome		HP:0001596	PMID:17314340	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-20]
OMIM:262000	Bjornstad syndrome		HP:0002299	PMID:15345881	PCS					P	HPO:probinson[2013-12-16]
OMIM:262000	Bjornstad syndrome		HP:0000407	PMID:17314340	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-20]
OMIM:262000	Bjornstad syndrome		HP:0003593	PMID:17314340	PCS		5/5			C	HPO:probinson[2022-03-20]
OMIM:262000	Bjornstad syndrome		HP:0000007	PMID:17314340	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-20]
OMIM:262000	Bjornstad syndrome		HP:0003329	OMIM:262000	TAS					P	HPO:probinson[2009-02-17]
OMIM:262000	Bjornstad syndrome		HP:0002208	OMIM:262000	TAS					P	HPO:probinson[2009-02-17]
OMIM:262000	Bjornstad syndrome		HP:0000135	PMID:17314340	PCS		0/3			P	HPO:probinson[2013-12-16];HPO:probinson[2022-03-20]
OMIM:262000	Bjornstad syndrome		HP:0001249	OMIM:262000	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:262000	Bjornstad syndrome		HP:0011359	OMIM:262000	TAS					P	HPO:probinson[2013-12-16]
OMIM:262000	Bjornstad syndrome		HP:0003777	PMID:17314340	PCS		5/5			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-03-20]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001298	PMID:28757203	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0002188	PMID:28757203	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001332	PMID:28757203	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0002120	PMID:28757203	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001250	PMID:28757203	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0012707	PMID:28757203	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-25]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001252	PMID:28757203	PCS		2/3			P	HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:6000830	OMIM:617668	TAS					P	HPO:probinson[2024-08-03]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0002119	PMID:28757203	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-25]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001522	PMID:28757203	PCS		2/3			C	HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0003348	PMID:28757203	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0003128	PMID:28757203	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0003623	PMID:28757203	PCS		3/3			C	HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0008936	PMID:28757203	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0007109	PMID:28757203	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0006956	PMID:28757203	PCS		2/3			P	HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0000252	PMID:28757203	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001344	PMID:28757203	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-06-25]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0031518	PMID:28757203	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-25]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0003542	PMID:28757203	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0011968	PMID:28757203	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0002154	PMID:28757203	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-25]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001263	PMID:28757203	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-25]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0002151	PMID:28757203	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0001285	PMID:28757203	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0002194	PMID:28757203	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-25]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0012736	PMID:28757203	PCS		3/3			P	HP:probinson[2019-01-04];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0002093	PMID:28757203	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0000007	PMID:28757203	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617668	Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities		HP:0009879	PMID:28757203	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0008936	PMID:22002931	PCS		1/9			P	HPO:probinson[2021-09-26]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0002121	PMID:22002931	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0001263	PMID:22002931	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0001328	PMID:22002931	PCS		2/4	FEMALE		P	HPO:probinson[2021-09-26]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0001417	PMID:22002931	PCS					I	HPO:probinson[2013-01-09]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0001423	PMID:9106537	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0001249	PMID:22002931	PCS					P	HPO:probinson[2013-02-22]
OMIM:300849	Intellectual developmental disorder, X-linked 41		HP:0001249	PMID:22002931	PCS		9/9	MALE		P	HPO:probinson[2021-09-26]
OMIM:619645	Spermatogenic failure 59		HP:0003251	PMID:33211200	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619645	Spermatogenic failure 59		HP:0011462	PMID:33211200	PCS		3/3			C	HPO:probinson[2022-02-08]
OMIM:619645	Spermatogenic failure 59		HP:0000007	PMID:33211200	PCS					I	HPO:probinson[2022-02-08]
OMIM:619645	Spermatogenic failure 59		HP:0031038	PMID:33211200	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:619645	Spermatogenic failure 59		HP:0011961	PMID:33211200	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0005425	PMID:26279205	PCS		2/20			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0025452	PMID:26279205	PCS		1/20			P	HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0004313	PMID:26279205	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0003621	PMID:26279205	PCS		1/13			C	HPO:probinson[2022-04-27]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0001596	PMID:26279205	PCS		3/20			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0002582	PMID:26279205	PCS		1/20			P	HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0002110	PMID:26279205	PCS		2/20			P	HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0005387	PMID:26279205	PCS		14/20			P	HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0001890	PMID:26279205	PCS		2/20			P	HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0003581	PMID:26279205	PCS		10/13			C	HPO:probinson[2022-04-27]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0001581	PMID:26279205	PCS		1/20			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0011108	PMID:26279205	PCS		3/20			P	HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0002719	PMID:26279205	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0011463	PMID:26279205	IEA		2/13			C	HPO:probinson[2022-04-27]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0006510	PMID:26279205	PCS		4/20			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0006532	PMID:26279205	PCS		8/20			P	HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0001873	PMID:26279205	PCS		3/20			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-09]
OMIM:616576	Immunodeficiency, common variable, 12		HP:0000006	PMID:26279205	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-09]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0004523	OMIM:614407	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000343	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001332	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001252	OMIM:614407	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001290	OMIM:614407	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0002080	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0009183	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001508	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000337	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0100807	OMIM:614407	TAS					P	HPO:skoehler[2013-04-09]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000179	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001347	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000253	OMIM:614407	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000395	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000252	OMIM:614407	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001344	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0002078	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001662	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001321	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0002079	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001063	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0040270	OMIM:614407	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001182	OMIM:614407	TAS					P	HPO:skoehler[2013-04-09]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000448	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000007	OMIM:614407	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0004209	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0000400	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001510	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0002500	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001678	OMIM:614407	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0001952	OMIM:614407	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614407	Microcephaly, cerebellar hypoplasia, and cardiac conduction defect syndrome		HP:0009879	OMIM:614407	TAS					P	HPO:skoehler[2014-11-26]
OMIM:266500	Refsum disease		HP:0000662	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0003474	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0001251	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0003690	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0011675	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0012211	OMIM:266500	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:266500	Refsum disease		HP:0000518	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0000639	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0007141	OMIM:266500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:266500	Refsum disease		HP:0000616	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0010571	OMIM:266500	TAS					P	HPO:probinson[2013-11-24]
OMIM:266500	Refsum disease		HP:0000458	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0000510	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0002654	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0001265	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0001640	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0001761	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:4000163	PMID:9326940;PMID:2433405	PCS		20/20			P	HPO:probinson[2023-03-31];HPO:probinson[2024-01-13]
OMIM:266500	Refsum disease		HP:0008064	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0000407	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0000508	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0000007	OMIM:266500	IEA					I	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0000546	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0001635	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:266500	Refsum disease		HP:0001638	OMIM:266500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266500	Refsum disease		HP:0002922	OMIM:266500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:266500	Refsum disease		HP:0004689	OMIM:266500	IEA					P	HPO:iea[2009-02-17]
OMIM:612076	Hypouricemia, renal, 2		HP:0000007	OMIM:612076	TAS					I	HPO:skoehler[2015-12-30]
OMIM:612076	Hypouricemia, renal, 2		HP:0003537	PMID:19026395	PCS					P	HPO:probinson[2013-01-09]
OMIM:612076	Hypouricemia, renal, 2		HP:0000006	PMID:19026395	PCS					I	HPO:probinson[2013-04-04]
OMIM:612076	Hypouricemia, renal, 2		HP:0000787	OMIM:612076	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000582	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0003577	PMID:32307552	PCS		2/2			C	HPO:probinson[2022-08-16];HPO:probinson[2022-08-16]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0001156	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0410030	PMID:32307552	PCS		2/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0001629	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0001746	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000316	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0008872	PMID:32307552	PCS		2/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0006695	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000411	PMID:32307552	PCS		2/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0001642	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0001320	PMID:32307552	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000175	PMID:32307552	PCS		2/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000252	PMID:32307552	PCS		2/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0003363	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0001263	PMID:32307552	PCS		2/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0012385	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0002808	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0008386	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000007	PMID:32307552	PCS					I	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000601	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0007477	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0004209	PMID:32307552	PCS		2/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000347	PMID:32307552	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619123	Cardiofacioneurodevelopmental syndrome		HP:0000028	PMID:32307552	PCS		1/1	MALE		P	HPO:probinson[2021-02-14]
OMIM:606003	Transaldolase deficiency		HP:0001410	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0002002	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0000260	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001395	OMIM:606003	TAS	HP:0003577				P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001394	PMID:11283793	PCS					P	HPO:probinson[2013-01-09]
OMIM:606003	Transaldolase deficiency		HP:0002240	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001629	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001508	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001903	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001009	PMID:11283793	PCS					P	HPO:probinson[2013-02-23]
OMIM:606003	Transaldolase deficiency		HP:0001643	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001744	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0000154	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001562	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0000233	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0002033	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0002099	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001680	PMID:11283793	PCS					P	HPO:probinson[2013-02-23]
OMIM:606003	Transaldolase deficiency		HP:0000470	OMIM:606003	IEA					P	HPO:skoehler[2019-09-07]
OMIM:606003	Transaldolase deficiency		HP:0005280	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001518	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0000007	PMID:11283793	PCS					I	HPO:probinson[2013-02-23]
OMIM:606003	Transaldolase deficiency		HP:0008665	PMID:11283793	PCS					P	HPO:probinson[2013-02-23]
OMIM:606003	Transaldolase deficiency		HP:0000664	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001511	OMIM:606003	TAS					P	HPO:skoehler[2015-12-30]
OMIM:606003	Transaldolase deficiency		HP:0001433	PMID:11283793	PCS					P	HPO:probinson[2013-02-23]
OMIM:606003	Transaldolase deficiency		HP:0001631	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0000322	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001873	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0000369	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0000325	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001876	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001413	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:606003	Transaldolase deficiency		HP:0001655	OMIM:606003	TAS					P	HPO:skoehler[2015-07-26]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0025708	PMID:15317892	PCS		1/1			C	HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0032073	PMID:15317892	PCS		1/1			P	HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0000122	PMID:15317892	PCS		1/1			P	HPO:iea[2010-05-11];HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0000151	PMID:15317892	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0000811	PMID:15317892	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0003250	PMID:15317892	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0001061	PMID:15317892	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0034589	PMID:15317892	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0000006	PMID:15317892	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0001007	OMIM:158330	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0025380	PMID:15317892	PCS		1/1			P	HPO:probinson[2023-03-21]
OMIM:158330	Mullerian aplasia and hyperandrogenism		HP:0000786	PMID:15317892	PCS		1/1			P	HPO:probinson[2023-03-21]
OMIM:118700	Chorea, benign hereditary		HP:0001288	OMIM:118700	IEA					P	HPO:iea[2009-02-17]
OMIM:118700	Chorea, benign hereditary		HP:0001260	OMIM:118700	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:118700	Chorea, benign hereditary		HP:0000726	PMID:12891678	PCS		0/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-26]
OMIM:118700	Chorea, benign hereditary		HP:0011463	PMID:12891678	PCS		2/4			C	HPO:probinson[2022-11-26]
OMIM:118700	Chorea, benign hereditary		HP:0000739	OMIM:118700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:118700	Chorea, benign hereditary		HP:0003593	PMID:12891678	PCS		2/4			C	HPO:probinson[2022-11-26]
OMIM:118700	Chorea, benign hereditary		HP:0002072	PMID:12891678	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:118700	Chorea, benign hereditary		HP:0001270	PMID:12891678	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:118700	Chorea, benign hereditary		HP:0002359	PMID:12891678	PCS		1/4			P	HPO:probinson[2022-11-26]
OMIM:118700	Chorea, benign hereditary		HP:0000006	PMID:11971878	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0002311	PMID:23611888	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0002078	PMID:23611888;PMID:24078737	PCS		7/7			P	HPO:probinson[2021-02-20];HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0000750	PMID:24078737	PCS		4/4			P	HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0003487	PMID:23611888	PCS		2/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001310	PMID:23611888	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001272	PMID:23611888	PCS		3/3		HP:0012828	P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001371	PMID:24078737	PCS		1/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001260	PMID:23611888	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0002066	PMID:23611888	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001263	PMID:23611888;PMID:24078737	PCS		7/7			P	HPO:probinson[2021-02-20];HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001252	PMID:23611888;PMID:24078737	PCS		6/7			P	HPO:probinson[2021-02-20];HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001251	PMID:23611888;PMID:24078737	PCS		7/7			P	HPO:probinson[2021-02-20];HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0002075	PMID:23611888	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0003593	PMID:23611888	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0000639	PMID:23611888	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0000657	PMID:23611888	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0000007	PMID:23611888	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0000565	PMID:23611888	PCS		1/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0000543	PMID:23611888	PCS		1/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001249	PMID:24078737	PCS		4/4			P	HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0000666	PMID:24078737	PCS		3/4			P	HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0001347	PMID:23611888	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-20]
OMIM:616204	Spinocerebellar ataxia, autosomal recessive 18		HP:0006855	PMID:24078737	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0001155	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0003411	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0003365	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0006429	OMIM:609324	TAS					P	HPO:probinson[2012-06-08]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0004322	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0004582	OMIM:609324	TAS				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0100864	OMIM:609324	TAS					P	HPO:probinson[2012-06-08]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0002829	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0000926	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0006398	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0002812	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0002834	OMIM:609324	TAS					P	HPO:probinson[2015-03-21]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0002857	OMIM:609324	IEA					P	HPO:iea[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0002656	OMIM:609324	TAS					P	HPO:probinson[2009-02-17]
OMIM:609324	Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia		HP:0000006	OMIM:609324	IEA					I	HPO:iea[2009-02-17]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0001298	PMID:19167255	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0008936	PMID:12754703	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0000252	OMIM:618229	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0002376	OMIM:618229	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0011968	PMID:12754703	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0003593	OMIM:618229	IEA					C	HPO:skoehler[2019-02-15]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0001290	OMIM:618229	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0011923	PMID:19167255;PMID:12754703	PCS		2/2			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0012444	OMIM:618229	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0001508	PMID:12754703	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0000639	OMIM:618229	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0001639	PMID:19167255;PMID:12754703	PCS		2/2			P	HPO:probinson[2023-02-11];HPO:skoehler[2019-04-18];HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0000007	PMID:12754703	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0000648	OMIM:618229	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0001522	PMID:12754703	PCS		1/1			C	HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0001257	OMIM:618229	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0003128	PMID:12754703	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-11]
OMIM:618229	Mitochondrial complex I deficiency, nuclear type 7		HP:0003623	PMID:12754703	PCS		1/1			C	HPO:probinson[2023-02-11]
OMIM:155600	Melanoma, cutaneous malignant		HP:0012056	OMIM:155600	TAS					P	HPO:skoehler[2010-06-18]
OMIM:155600	Melanoma, cutaneous malignant		HP:0007716	OMIM:155600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:155600	Melanoma, cutaneous malignant		HP:0001074	OMIM:155600	IEA					P	HPO:skoehler[2009-02-17]
OMIM:155600	Melanoma, cutaneous malignant		HP:0001062	OMIM:155600	IEA					P	HPO:iea[2009-02-17]
OMIM:155600	Melanoma, cutaneous malignant		HP:0001054	OMIM:155600	IEA					P	HPO:iea[2009-02-17]
OMIM:155600	Melanoma, cutaneous malignant		HP:0000006	OMIM:155600	IEA					I	HPO:iea[2009-02-17]
OMIM:155600	Melanoma, cutaneous malignant		HP:0000478	OMIM:155600	IEA					P	HPO:iea[2009-02-17]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0003411	PMID:21910225	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0003577	PMID:21910225	PCS		1/7			C	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0008905	PMID:21910225	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0004322	PMID:21910225;PMID:26167768	PCS		9/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0005257	OMIM:602271	TAS					P	HPO:probinson[2009-02-17]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0003375	OMIM:602271	TAS					P	HPO:probinson[2009-02-17]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0003593	PMID:21910225	PCS		2/7			C	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0012207	PMID:26167768	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0100864	OMIM:602271	TAS					P	HPO:probinson[2009-02-17]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000639	PMID:21910225	PCS		2/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0011463	PMID:21910225	PCS		1/7			C	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0002812	PMID:21910225	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0006532	PMID:26167768	PCS		1/11			P	HPO:probinson[2012-07-16];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000510	PMID:21910225;PMID:26167768	PCS		20/21			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000774	PMID:26167768	PCS		3/11			P	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0002657	PMID:26167768	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0001744	PMID:26167768	PCS		2/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0003623	PMID:21910225	PCS		1/7			C	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0003521	PMID:21910225	PCS		4/7			P	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0003621	PMID:21910225	PCS		2/7			C	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0002650	PMID:21910225;PMID:26167768	PCS		8/18			P	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0002091	PMID:26167768	PCS		2/11			P	HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000907	PMID:21910225	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000926	PMID:21910225	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000007	PMID:26167768	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000546	PMID:21910225	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000648	PMID:21910225	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:602271	Spondylometaphyseal dysplasia, axial		HP:0000548	PMID:26167768	PCS	HP:0011463	10/11			P	HPO:probinson[2022-09-08]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0001265	PMID:32943585	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0006858	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0003596	PMID:32943585	PCS		2/2			C	HPO:probinson[2024-03-14];HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0003487	PMID:32943585	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0001288	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0001260	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0002066	PMID:32943585	PCS		2/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0001284	OMIM:608984	IEA					P	HPO:iea[2009-02-17]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0010871	PMID:32943585	PCS		2/2			P	HPO:skoehler[2015-01-27];HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0012534	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0007670	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0007078	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0001317	PMID:32943585	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0003409	PMID:32943585	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0002359	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0006962	OMIM:608984	IEA					P	HPO:iea[2009-02-17]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0002403	OMIM:608984	IEA		1/2			P	HPO:iea[2009-02-17]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0006886	PMID:32943585	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:608984	Ataxia, sensory, autosomal dominant		HP:0000006	PMID:21115467	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0032989	PMID:33704598	PCS		2/2			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0008936	PMID:34631954;PMID:33704598	PCS		5/5			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0002421	PMID:33704598	PCS		2/2			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0000750	PMID:34631954;PMID:33704598	PCS		5/5			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0001332	PMID:34631954;PMID:33704598	PCS		5/5			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0002365	PMID:33704598	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0031936	PMID:34631954	PCS		3/3			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0001263	PMID:34631954;PMID:33704598	PCS		5/5			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0003593	PMID:34631954;PMID:33704598	PCS		5/5			C	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0033725	PMID:34631954	PCS		3/3			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0010864	PMID:34631954;PMID:33704598	PCS		4/5			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0001508	PMID:33704598	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0003819	PMID:34631954	PCS		1/3			C	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0000817	PMID:33704598	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0000739	PMID:34631954	PCS		3/3			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0000007	PMID:33704598	PCS					I	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0000722	PMID:34631954	PCS		3/3			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0001638	PMID:34631954	PCS		1/3			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0000713	PMID:33704598	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0025336	PMID:34631954	PCS		3/3			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0001337	PMID:34631954	PCS		3/3			P	HPO:probinson[2022-02-18]
OMIM:619651	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia		HP:0001336	PMID:34631954	PCS		3/3			P	HPO:probinson[2022-02-18]
OMIM:616562	Retinitis pigmentosa 74		HP:0001133	PMID:25541840	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0003596	PMID:25541840	PCS		1/9			C	HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0003584	PMID:25541840	PCS		1/9			C	HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0000580	PMID:25541840	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0010442	PMID:25541840	PCS		1/9			P	HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0012210	PMID:25541840	PCS		0/9			P	HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0011463	PMID:25541840	PCS		1/9			C	HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0011462	PMID:25541840	PCS		6/9			C	HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0000007	PMID:25541840	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0007663	PMID:25541840	PCS		8/8			P	HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0000543	PMID:25541840	PCS				HP:0012826	P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0001115	PMID:25541840	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0000510	PMID:25541840	PCS		9/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-17]
OMIM:616562	Retinitis pigmentosa 74		HP:0001513	PMID:25541840	PCS		1/9			P	HPO:probinson[2022-12-17]
OMIM:272950	Teebi-Shaltout syndrome		HP:0030799	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000385	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0001650	OMIM:272950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000341	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0004322	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000160	OMIM:272950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000262	OMIM:272950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000085	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0008070	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0010291	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0001629	OMIM:272950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000319	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0011220	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0009487	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000316	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000954	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0006610	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000455	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0002217	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0001840	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000677	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000154	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0002553	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000252	OMIM:272950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000175	OMIM:272950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000431	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0001762	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000430	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000294	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000071	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0012385	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0001838	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000506	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000508	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0002825	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000767	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000007	PMID:23918592	PCS					I	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0002705	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000568	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0008589	PMID:23918592	PCS					P	HPO:probinson[2017-06-20]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000768	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0001159	OMIM:272950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000369	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272950	Teebi-Shaltout syndrome		HP:0000126	OMIM:272950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0003510	PMID:27380894	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0000365	PMID:27380894	PCS		0/8			P	HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0008905	PMID:27380894	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0002650	PMID:27380894	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0004586	PMID:27380894	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0001382	PMID:27380894	PCS		0/8			P	HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0030674	PMID:27380894	PCS		7/7			C	HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0000592	PMID:27380894	PCS		1/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0001419	PMID:27380894	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0000938	PMID:27380894	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0002979	PMID:27380894	PCS		8/8			P	HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0000767	PMID:27380894	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0008422	PMID:27380894	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0000703	PMID:27380894	PCS		0/8			P	HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0002757	PMID:27380894	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0006488	PMID:27380894	PCS		7/8			P	HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0000768	PMID:27380894	PCS		3/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:301014	Osteogenesis imperfecta, type XIX		HP:0005855	PMID:27380894	PCS		7/8			P	HPO:probinson[2023-02-17]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0000594	PMID:19836009	PCS		6/7			P	HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0001156	PMID:19836009	PCS		0/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0004322	PMID:19836009	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0001387	PMID:19836009	PCS		0/7			P	HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0007906	PMID:19836009	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0012629	OMIM:613195	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0011484	PMID:19836009	PCS		5/7			P	HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0000007	PMID:19836009	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0001083	PMID:19836009	PCS					P	HPO:skoehler[2013-01-27];HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0011003	PMID:19836009	PCS		7/7			P	HPO:probinson[2023-02-23];HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0000501	PMID:19836009	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:613195	Weill-Marchesani syndrome 4		HP:0100693	OMIM:613195	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614822	Spermatogenic failure 10		HP:0003251	PMID:22275165	PCS		2/2			P	HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:614822	Spermatogenic failure 10		HP:0011462	PMID:22275165	PCS		2/2			C	HPO:probinson[2022-12-18]
OMIM:614822	Spermatogenic failure 10		HP:0012207	PMID:22275165	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:614822	Spermatogenic failure 10		HP:0000006	PMID:22479503	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-18]
OMIM:614822	Spermatogenic failure 10		HP:0012864	PMID:22275165	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-12-18]
OMIM:614822	Spermatogenic failure 10		HP:0000798	PMID:22275165	PCS		1/2			P	HPO:probinson[2022-12-18]
OMIM:201000	Carpenter syndrome 1		HP:0000286	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0007759	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001770	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0004322	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0004443	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-02-24]
OMIM:201000	Carpenter syndrome 1		HP:0004442	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-02-24]
OMIM:201000	Carpenter syndrome 1		HP:0000482	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0004440	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0010093	PMID:17503333	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0006397	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0002857	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001643	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001841	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001642	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001840	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001249	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0009608	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0002673	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0003241	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0004097	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0011800	OMIM:201000	TAS					P	HPO:skoehler[2013-11-28]
OMIM:201000	Carpenter syndrome 1		HP:0012385	OMIM:201000	TAS					P	HPO:skoehler[2013-10-22]
OMIM:201000	Carpenter syndrome 1		HP:0000407	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0009891	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0001537	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000327	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0002869	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0000007	OMIM:201000;ISBN-13:978-0721606156	PCS					I	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000648	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001539	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000405	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0004209	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0002700	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0000960	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0000248	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000369	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000126	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0006349	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0004467	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001156	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0003298	OMIM:201000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201000	Carpenter syndrome 1		HP:0010194	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0001629	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0010275	PMID:17503333	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0001669	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001748	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0009843	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0000218	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0006335	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000377	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0002059	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0002650	OMIM:201000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201000	Carpenter syndrome 1		HP:0002970	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-02-25]
OMIM:201000	Carpenter syndrome 1		HP:0001162	PMID:17503333	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000072	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000470	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000272	OMIM:201000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201000	Carpenter syndrome 1		HP:0003182	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0005280	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0007370	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0000826	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0009473	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000506	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-04-27]
OMIM:201000	Carpenter syndrome 1		HP:0001636	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001631	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000028	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0000347	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:201000	Carpenter syndrome 1		HP:0001513	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0001276	PMID:23033978	PCS		1/1			P	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0002510	PMID:23603762	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0000252	PMID:23603762	PCS	HP:0003577	1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0001773	PMID:23033978	PCS		1/1			P	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0001344	PMID:23033978	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0002079	PMID:23603762	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0001250	PMID:23033978	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0001263	PMID:23033978	PCS					P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0005484	PMID:23033978	PCS		1/1			P	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0011461	PMID:23603762	PCS		4/4			C	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0002539	PMID:23033978	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0000733	PMID:23033978	PCS		1/1			P	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0020221	PMID:23603762	PCS		1/1			P	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0002804	PMID:23603762	PCS	HP:0011461	1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0100716	PMID:23033978	PCS		1/1			P	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0001989	PMID:23603762	PCS	HP:0011461	3/3			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0200055	PMID:23033978	PCS		1/1			P	HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0001511	PMID:23603762	PCS	HP:0011461	1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0002126	PMID:23603762	PCS		4/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:615282	Cortical dysplasia, complex, with other brain malformations 2		HP:0000006	PMID:23603762	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2021-05-04]
OMIM:616947	Premature ovarian failure 12		HP:0000007	PMID:25062452	PCS					I	HPO:probinson[2017-06-23]
OMIM:616947	Premature ovarian failure 12		HP:0000568	PMID:25062452	PCS					P	HPO:probinson[2017-06-23]
OMIM:616947	Premature ovarian failure 12		HP:0007754	PMID:25062452	PCS					P	HPO:probinson[2017-06-23]
OMIM:616947	Premature ovarian failure 12		HP:0000786	PMID:25062452	PCS					P	HPO:probinson[2017-06-23]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0002169	OMIM:617481	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0003577	PMID:28334956	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0003676	PMID:28334956	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000340	OMIM:617481	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000189	OMIM:617481	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0002540	PMID:28334956	PCS		15/15			P	HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0002188	PMID:28334956	PCS		5/13			P	HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001272	PMID:28334956	PCS		2/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0002120	PMID:28334956	PCS		5/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001250	PMID:28334956	PCS		6/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001252	PMID:28334956	PCS		15/15			P	HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000518	PMID:28334956	PCS	HP:0003577	3/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000411	OMIM:617481	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001347	PMID:28334956	PCS		12/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0003202	PMID:28334956	PCS		7/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000252	PMID:28334956	PCS		15/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0002650	OMIM:617481	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001762	OMIM:617481	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001344	PMID:28334956	PCS		15/15			P	HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0002079	PMID:28334956	PCS		4/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001285	PMID:28334956	PCS		14/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0012736	PMID:28334956	PCS		15/15			P	HP:probinson[2019-01-04];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0034392	PMID:28334956	PCS		7/8			P	HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000007	PMID:28334956	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001558	OMIM:617481	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000648	PMID:28334956	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000400	OMIM:617481	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0001357	PMID:28334956	PCS		13/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0000520	OMIM:617481	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617481	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies		HP:0002500	PMID:28334956	PCS		5/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000684	PMID:21741611	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0004443	PMID:21741611	PCS		4/6			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000243	OMIM:614188	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0004322	PMID:21741611	PCS		1/3			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0004442	PMID:21741611	PCS		6/6			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0001250	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0003396	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0004440	PMID:21741611	PCS		8/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0011455	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0010055	PMID:21741611	PCS		4/4			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0011463	PMID:30811827	PCS		2/2			C	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000316	OMIM:614188	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000678	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0004439	PMID:30811827	PCS		2/2			P	HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0005469	PMID:21741611	PCS		1/4			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000494	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0004691	PMID:21741611	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0011800	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0011330	PMID:21741611	PCS		8/8			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000327	PMID:21741611;PMID:30811827	PCS		9/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0002308	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000007	PMID:21741611	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000689	PMID:30811827	PCS		2/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000405	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000444	PMID:21741611	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000520	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000248	PMID:21741611;PMID:30811827	PCS		5/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000445	PMID:21741611	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0030799	OMIM:614188	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000263	PMID:21741611	PCS		1/4			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000340	PMID:21741611	PCS		2/7			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000189	PMID:21741611	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000381	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000262	OMIM:614188	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0001822	PMID:21741611	PCS		4/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0030084	OMIM:614188	TAS		HP:0040283			P	HPO:skoehler[2014-09-21]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000218	PMID:21741611	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0009803	PMID:21741611	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0001085	PMID:21741611	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0005487	PMID:21741611	PCS		1/4			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0011069	PMID:21741611	PCS		4/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0005280	PMID:21741611	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0100798	PMID:21741611	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000348	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000268	OMIM:614188	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0002007	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000389	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0000303	PMID:30811827	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614188	Craniosynostosis and dental anomalies		HP:0004425	PMID:21741611	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20]
OMIM:132300	Epilepsy, reading		HP:0003621	OMIM:132300	TAS					C	HPO:iea[2009-02-17]
OMIM:132300	Epilepsy, reading		HP:0002353	OMIM:132300	TAS					P	HPO:probinson[2015-02-15]
OMIM:132300	Epilepsy, reading		HP:0001250	OMIM:132300	TAS					P	HPO:probinson[2009-02-17]
OMIM:132300	Epilepsy, reading		HP:0000006	OMIM:132300	TAS					I	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0001891	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0006946	PMID:7996359	PCS		3/154			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0003212	PMID:17703096	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002783	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0005310	OMIM:301000	TAS					P	HPO:probinson[2012-06-11]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0001890	PMID:7996359;PMID:17703096	PCS		26/165			P	HPO:probinson[2021-07-03];HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0005353	PMID:7996359	PCS		19/154			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0003010	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0003593	PMID:17703096	PCS		11/11			C	HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0040184	OMIM:301000	TAS					P	HPO:skoehler[2015-10-05]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0012177	PMID:17703096	PCS		2/2			P	HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0000979	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0100806	PMID:7996359	PCS		13/154			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0001888	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0006532	PMID:7996359	PCS		50/154			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0001983	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0003347	PMID:7996359	PCS		32/94			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002971	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002850	OMIM:301000;PMID:17703096	PCS		11/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002014	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002037	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0001880	PMID:7996359	PCS		16/52			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0005523	PMID:17703096	PCS		2/11			P	HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0000112	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0003261	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0011944	PMID:17703096	PCS		1/11			P	HPO:probinson[2012-06-11];HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0011108	PMID:7996359	PCS		32/154			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0100279	PMID:17703096	PCS		1/11			P	HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0001419	PMID:7996359	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002848	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0000964	PMID:17703096	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0000403	PMID:7996359;PMID:17703096	PCS		83/165			P	HPO:probinson[2021-07-03];HPO:probinson[2022-05-06]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0000967	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002249	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002788	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0000421	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0001873	PMID:7996359;PMID:17703096	PCS		21/21			P	HPO:probinson[2022-05-06];HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0005537	PMID:7996359;PMID:17703096	PCS		63/63			P	HPO:probinson[2022-05-06];HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0000225	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002248	OMIM:301000	IEA					P	HPO:iea[2009-02-17]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002963	PMID:7996359	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0002028	PMID:7996359	PCS		13/154			P	HPO:probinson[2021-07-03]
OMIM:301000	Wiskott-Aldrich syndrome		HP:0005415	PMID:7996359;PMID:17703096	PCS		37/62			P	HPO:probinson[2021-07-03];HPO:probinson[2022-05-06]
OMIM:136600	Friedreich ataxia, so-called, with optic atrophy and sensorineuraldeafness		HP:0001265	OMIM:136600	IEA					P	HPO:iea[2009-02-17]
OMIM:136600	Friedreich ataxia, so-called, with optic atrophy and sensorineuraldeafness		HP:0000407	OMIM:136600	IEA					P	HPO:iea[2009-02-17]
OMIM:136600	Friedreich ataxia, so-called, with optic atrophy and sensorineuraldeafness		HP:0001251	OMIM:136600	IEA					P	HPO:iea[2009-02-17]
OMIM:136600	Friedreich ataxia, so-called, with optic atrophy and sensorineuraldeafness		HP:0000648	OMIM:136600	IEA					P	HPO:iea[2009-02-17]
OMIM:136600	Friedreich ataxia, so-called, with optic atrophy and sensorineuraldeafness		HP:0000006	OMIM:136600	IEA					I	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0002862	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001377	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000343	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001278	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001250	PMID:7842019	PCS		3/4			P	HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0003276	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0005792	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000939	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000916	OMIM:304150	TAS					P	HPO:probinson[2012-05-27]
OMIM:304150	Occipital horn syndrome		HP:0000978	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0002857	PMID:7842019	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0000218	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000977	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000015	OMIM:304150	IEA		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0000774	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001763	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000894	OMIM:304150	TAS					P	HPO:probinson[2012-05-27]
OMIM:304150	Occipital horn syndrome		HP:0000974	OMIM:304150	TAS		4/4		HP:0012825	P	HPO:probinson[2012-05-05];HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0002036	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000275	OMIM:304150	TAS					P	HPO:probinson[2012-05-01]
OMIM:304150	Occipital horn syndrome		HP:0000472	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0010837	PMID:7842019	PCS		4/5			P	HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0005302	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0002673	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000276	OMIM:304150	TAS					P	HPO:probinson[2012-05-01]
OMIM:304150	Occipital horn syndrome		HP:0001382	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0003066	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0004474	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001241	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001582	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001263	PMID:7842019	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0011967	PMID:7842019	PCS		5/5			P	HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0100777	PMID:7842019	PCS		3/4			P	HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0002808	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0001419	PMID:7842019	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0000926	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0006000	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000767	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000348	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0002208	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000768	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0000444	OMIM:304150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:304150	Occipital horn syndrome		HP:0001510	PMID:7842019	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0000885	OMIM:304150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304150	Occipital horn syndrome		HP:0002028	OMIM:304150	IEA		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:304150	Occipital horn syndrome		HP:0000126	OMIM:304150	IEA					P	HPO:iea[2009-02-17]
OMIM:304150	Occipital horn syndrome		HP:0003777	PMID:7842019	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0003774	PMID:30661770	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0003577	PMID:30661770	PCS		2/6			C	HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0003621	PMID:30661770	PCS		1/6			C	HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0011463	PMID:30661770	PCS		1/6			C	HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0000097	PMID:30661770	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0003581	PMID:30661770	PCS		1/6			C	HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0003593	PMID:30661770	PCS		1/6			C	HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0000093	PMID:30661770	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0001417	PMID:30661770	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:301028	Nephrotic syndrome, type 20		HP:0012588	PMID:30661770	PCS		6/6			P	HPO:probinson[2023-02-11]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0002908	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0001508	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0003155	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0003593	PMID:31863603	PCS		1/1			C	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0001405	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0000007	PMID:31863603	PCS					I	HPO:probinson[2021-10-17];HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0011888	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0030948	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0000978	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0001406	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0002910	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:619484	Cholestasis, progressive familial intrahepatic, 6		HP:0002028	PMID:31863603	PCS		1/1			P	HPO:probinson[2021-10-17]
OMIM:236690	Hydrocephalus, normal pressure, 1		HP:0001288	OMIM:236690	IEA					P	HPO:iea[2009-02-17]
OMIM:236690	Hydrocephalus, normal pressure, 1		HP:0002343	PMID:31004071	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-17]
OMIM:236690	Hydrocephalus, normal pressure, 1		HP:0000726	OMIM:236690	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236690	Hydrocephalus, normal pressure, 1		HP:0001263	OMIM:236690	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:236690	Hydrocephalus, normal pressure, 1		HP:0002607	OMIM:236690	TAS					P	HPO:probinson[2012-06-10]
OMIM:236690	Hydrocephalus, normal pressure, 1		HP:0000020	OMIM:236690	TAS					P	HPO:probinson[2012-06-10]
OMIM:236690	Hydrocephalus, normal pressure, 1		HP:0000006	PMID:31004071	PCS					I	HPO:probinson[2020-07-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0003577	PMID:21358632	PCS		3/3			C	HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000046	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0006628	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0004322	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002780	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000160	PMID:21358632	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000064	OMIM:613803	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002020	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0001270	OMIM:613803	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0010306	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0001508	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0012471	PMID:21358632	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0008551	PMID:21358632	PCS		3/3			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0006498	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002812	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002779	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0006532	OMIM:613803	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000774	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000773	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0001601	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000358	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002215	OMIM:613803	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000494	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000252	PMID:21358632	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000054	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000750	OMIM:613803	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0001762	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002750	PMID:21358632	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002970	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0003561	PMID:21358632	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0003187	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0011968	PMID:21358632	PCS		1/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0003100	PMID:21358632	PCS		1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0003065	PMID:21358632	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002094	OMIM:613803	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000308	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000327	PMID:21358632	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000426	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000007	PMID:21358632	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0006443	PMID:21358632	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0008665	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0001511	PMID:21358632	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000047	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000028	PMID:21358632	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000369	OMIM:613803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000347	PMID:21358632;OMIM:613803	PCS		13/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0002225	OMIM:613803	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613803	Meier-Gorlin syndrome 3		HP:0000325	OMIM:613803	TAS					P	HPO:skoehler[2012-10-17]
OMIM:125640	DERMOODONTODYSPLASIA		HP:0002552	PMID:6616948;OMIM:125640	PCS		20/20			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-10]
OMIM:125640	DERMOODONTODYSPLASIA		HP:0002164	PMID:6616948;OMIM:125640	PCS		20/20			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-10]
OMIM:125640	DERMOODONTODYSPLASIA		HP:0000958	PMID:6616948	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:125640	DERMOODONTODYSPLASIA		HP:0000968	PMID:6616948;OMIM:125640	PCS		20/20			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-10]
OMIM:125640	DERMOODONTODYSPLASIA		HP:0000668	PMID:6616948	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:125640	DERMOODONTODYSPLASIA		HP:0000006	OMIM:125640	IEA					I	HPO:iea[2009-02-17]
OMIM:125640	DERMOODONTODYSPLASIA		HP:0000963	PMID:6616948	PCS					P	HPO:lccarmody[2018-09-10]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0002474	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0003124	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0004322	PMID:34971397	PCS		1/2			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0030796	PMID:34971397	PCS		1/2			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0002173	PMID:34576089;PMID:34971397	PCS		3/3			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0001263	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0003593	PMID:34576089;PMID:34971397	PCS		3/3			C	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0012450	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0000007	PMID:34576089	PCS					I	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0001987	PMID:34576089;PMID:34971397	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0001943	PMID:34576089;PMID:34971397	PCS		3/3			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0000821	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0002925	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0007018	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0001510	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0001631	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620211	Hyperinsulinemic hypoglycemia, familial, 8		HP:0000842	PMID:34576089	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0002069	OMIM:607876	PCS		118/229			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0002076	PMID:31664034	PCS		42/130			P	HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0003581	PMID:31664034	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001340	OMIM:607876	IEA					P	HPO:iea[2009-02-17]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001351	OMIM:607876	IEA					P	HPO:iea[2009-02-17]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0003680	OMIM:607876	IEA					C	HPO:iea[2009-02-17]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001251	PMID:31664034	PCS		3/201			P	HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0010852	OMIM:607876	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0100543	OMIM:607876	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0000726	PMID:31664034	PCS		5/199			P	HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001312	OMIM:607876	IEA					P	HPO:iea[2009-02-17]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0000006	PMID:31664034	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001326	OMIM:607876	IEA					P	HPO:iea[2009-02-17]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001249	PMID:31664034	PCS		9/193			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001337	PMID:31664034	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-20]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0000643	OMIM:607876	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607876	Epilepsy, familial adult myoclonic, 2		HP:0001336	PMID:31664034	PCS		195/227			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:300322	Lesch-Nyhan syndrome		HP:0002421	PMID:35875183	PCS		1/1			P	HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0000121	PMID:22157001	PCS		13/17			P	HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0004322	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001332	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001250	PMID:22157001	PCS		1/20			P	HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001252	OMIM:300322	IEA		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0003593	PMID:35875183	PCS		2/2			C	HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001270	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0011463	PMID:22157001	PCS		8/23			C	HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0011462	PMID:22157001	PCS		2/23			C	HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001889	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001249	PMID:35875183	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0003149	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001347	OMIM:300322	TAS					P	HPO:probinson[2013-03-14]
OMIM:300322	Lesch-Nyhan syndrome		HP:0002179	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0002015	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0003621	PMID:22157001	PCS		7/23			C	HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0002013	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001266	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001260	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001263	PMID:35875183;PMID:22157001	PCS		23/23			P	HPO:probinson[2022-10-09];HPO:probinson[2022-10-09];HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0002071	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001419	PMID:22157001	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0002827	PMID:22157001	PCS		5/20			P	HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0000029	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0100716	PMID:22157001	PCS		18/20			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-09]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001257	OMIM:300322	TAS					P	HPO:probinson[2013-03-14]
OMIM:300322	Lesch-Nyhan syndrome		HP:0001854	OMIM:300322	TAS					P	HPO:probinson[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0000787	OMIM:300322	IEA					P	HPO:iea[2009-02-17]
OMIM:300322	Lesch-Nyhan syndrome		HP:0002149	PMID:35875183	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-09]
OMIM:200450	Achalasia-Microcephaly syndrome		HP:0000252	OMIM:200450	IEA					P	HPO:iea[2009-02-17]
OMIM:200450	Achalasia-Microcephaly syndrome		HP:0002571	OMIM:200450	IEA					P	HPO:iea[2009-02-17]
OMIM:200450	Achalasia-Microcephaly syndrome		HP:0000007	OMIM:200450	IEA					I	HPO:iea[2009-02-17]
OMIM:200450	Achalasia-Microcephaly syndrome		HP:0000565	OMIM:200450	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:200450	Achalasia-Microcephaly syndrome		HP:0001249	OMIM:200450	IEA					P	HPO:iea[2009-02-17]
OMIM:200450	Achalasia-Microcephaly syndrome		HP:0001007	OMIM:200450	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:123557	Cryptotia, familial		HP:0011252	OMIM:123557	IEA					P	HPO:skoehler[2015-01-27]
OMIM:123557	Cryptotia, familial		HP:0000356	OMIM:123557	IEA					P	HPO:skoehler[2009-02-17]
OMIM:123557	Cryptotia, familial		HP:0000006	OMIM:123557	IEA					I	HPO:iea[2009-02-17]
OMIM:615527	Candidiasis, familial, 8		HP:0003621	PMID:24120361	PCS		1/2			C	HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0009098	PMID:24120361	PCS		2/2			P	HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0100825	PMID:24120361	PCS		1/2			P	HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0011463	PMID:24120361	PCS		1/2			C	HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0001051	PMID:24120361	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0000007	PMID:24120361	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0000158	PMID:24120361	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0000498	PMID:24120361	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-02]
OMIM:615527	Candidiasis, familial, 8		HP:0012203	PMID:24120361	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-02]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0003236	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0010628	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0003577	PMID:17634419	PCS		4/4			C	HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000486	PMID:17634419	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0002540	PMID:17634419	PCS		4/4			P	HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0002120	PMID:17634419	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001371	OMIM:613156	TAS					P	HPO:skoehler[2013-05-31]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0025169	OMIM:613156	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001252	PMID:17634419	PCS	HP:0003577	4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000580	PMID:17634419	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001290	OMIM:613156	TAS	HP:0003577				P	HPO:skoehler[2017-07-13]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001270	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0003307	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0002119	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000158	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0003701	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001265	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001320	PMID:17634419	PCS		4/4			P	HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0003324	OMIM:613156;PMID:17634419	PCS		14/14			P	HPO:probinson[2023-01-26];HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000252	PMID:17634419	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000054	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0002650	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001321	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0002079	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000194	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001284	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0003560	OMIM:613156	TAS		20/20			P	HPO:skoehler[2015-01-19];HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0002093	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0002827	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000007	PMID:17634419	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0001712	OMIM:613156	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0003712	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000028	OMIM:613156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613156	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2		HP:0000545	PMID:17634419	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:618003	Deafness, autosomal recessive 57		HP:0001751	PMID:29048736	PCS		0/3			P	HPO:skoehler[2018-10-08];HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:618003	Deafness, autosomal recessive 57		HP:0000365	PMID:26416264	PCS	HP:0003593	12/12			P	HP:probinson[2019-03-02]
OMIM:618003	Deafness, autosomal recessive 57		HP:0000407	PMID:26849169	PCS	HP:0003593	2/2			P	HP:probinson[2019-03-02]
OMIM:618003	Deafness, autosomal recessive 57		HP:0011463	PMID:29048736	PCS					C	HPO:probinson[2024-03-15]
OMIM:618003	Deafness, autosomal recessive 57		HP:0003593	PMID:29048736	PCS					C	HPO:probinson[2024-03-15]
OMIM:618003	Deafness, autosomal recessive 57		HP:0000007	PMID:26416264;OMIM:618003	PCS		20/20			I	HP:probinson[2019-03-02];HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:618003	Deafness, autosomal recessive 57		HP:0000505	PMID:29048736	PCS		0/4			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:618003	Deafness, autosomal recessive 57		HP:0000479	PMID:29048736	PCS		0/1			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:306960	Hhhh syndrome		HP:0100556	OMIM:306960	TAS					P	HPO:skoehler[2012-10-17]
OMIM:306960	Hhhh syndrome		HP:0001250	OMIM:306960	IEA					P	HPO:iea[2009-02-17]
OMIM:306960	Hhhh syndrome		HP:0000924	OMIM:306960	IEA					P	HPO:iea[2009-02-17]
OMIM:306960	Hhhh syndrome		HP:0001419	OMIM:306960	TAS					I	HPO:skoehler[2017-07-13]
OMIM:306960	Hhhh syndrome		HP:0001269	OMIM:306960	IEA					P	HPO:iea[2009-02-17]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002421	PMID:28017370	PCS	HP:0003593				P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000483	PMID:28017370	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000486	PMID:28017373;PMID:28017372	PCS		11/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0004322	PMID:28017370	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001250	PMID:28017373	PCS		2/9			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002066	PMID:28017370	PCS		5/7			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0003593	PMID:28017372	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002020	PMID:28017373	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001251	PMID:28017373	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001290	PMID:28017370	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000319	PMID:28017373	PCS		2/10			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0011220	PMID:28017372;PMID:28017370	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000316	PMID:28017373;PMID:28017370	PCS		3/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000358	PMID:28017373	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001249	PMID:28017373	PCS		9/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0003623	PMID:28017370	PCS		5/8			C	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000252	PMID:28017370	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000054	PMID:28017372	PCS		1/1	MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000494	PMID:28017372	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002078	PMID:28017370	PCS		5/8			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000574	PMID:28017370	PCS		2/8			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000331	PMID:28017373	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001260	PMID:28017373;PMID:28017370	PCS		4/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000490	PMID:28017370	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001263	PMID:28017373;PMID:28017372	PCS		12/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001182	PMID:28017370	PCS		2/8			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0011098	PMID:28017372	PCS		1/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000369	PMID:28017373;PMID:28017370	PCS		5/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000325	PMID:28017372	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000006	PMID:28017373	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0008947	PMID:28017373;PMID:28017372	PCS	HP:0003593	5/13			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000385	PMID:28017373	PCS		2/8			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000582	PMID:28017373;PMID:28017370	PCS		3/18			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001310	PMID:28017370	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000463	PMID:28017372	PCS		1/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002002	PMID:28017373	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001272	PMID:28017370	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0010862	PMID:28017372	PCS		1/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001270	PMID:28017373	PCS		9/10			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0030319	PMID:28017372	PCS		3/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0007021	PMID:28017372	PCS		2/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000337	PMID:28017370	PCS		2/8			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000733	PMID:28017372	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000219	PMID:28017373	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002714	PMID:28017372;PMID:28017370	PCS		2/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000537	PMID:28017372	PCS		1/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000455	PMID:28017370	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000179	PMID:28017373	PCS		2/10			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000215	PMID:28017373	PCS		2/10			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002058	PMID:28017370	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000396	PMID:28017372	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001562	PMID:28017372	PCS	HP:0011461	1/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001320	PMID:28017373;PMID:28017372	PCS		4/10			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0008936	PMID:28017373	PCS		3/10			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002015	PMID:28017372	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000076	PMID:28017373;PMID:28017370	PCS		4/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0002136	PMID:28017372	PCS		3/3			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000750	PMID:28017373;PMID:28017370	PCS		14/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0031936	PMID:28017370	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000276	PMID:28017373	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0003186	PMID:28017372	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0011822	PMID:28017373	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0011228	PMID:28017373	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000426	PMID:28017373	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0001558	PMID:28017372	PCS	HP:0011461	2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000348	PMID:28017373	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000664	PMID:28017370	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000268	PMID:28017370	PCS		1/8			P	HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000300	PMID:28017372	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:617330	Hypotonia, ataxia, and delayed development syndrome		HP:0000028	PMID:28017370	PCS		1/4	MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0005356	OMIM:235400	TAS					P	HPO:skoehler[2012-11-18]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001250	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0003077	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0005575	OMIM:235400	TAS					P	HPO:probinson[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0002381	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0100543	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0000979	OMIM:235400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001923	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001945	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001269	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0002014	OMIM:235400	TAS					P	HPO:skoehler[2012-11-18]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0005369	OMIM:235400	TAS					P	HPO:skoehler[2012-11-18]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001981	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0005421	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001919	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001937	OMIM:235400	TAS					P	HPO:probinson[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0000822	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0000007	OMIM:235400	IEA					I	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0100519	OMIM:235400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001873	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0000006	OMIM:235400	IEA					I	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0003138	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0003259	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0005416	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:235400	Hemolytic uremic syndrome, atypical, susceptibility to, 1		HP:0001259	OMIM:235400	IEA					P	HPO:iea[2009-02-17]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0001132	PMID:31274573	PCS		2/2			P	HPO:probinson[2023-01-23];HPO:probinson[2023-01-23]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0012629	PMID:31274573	PCS		2/4			P	HPO:probinson[2023-01-23];HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0031624	PMID:31274573	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0009381	PMID:31274573	PCS		1/2			P	HPO:probinson[2023-01-23]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000518	PMID:30194805	PCS		10/12			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0011463	PMID:31274573	PCS		3/4			C	HPO:probinson[2023-01-23];HPO:probinson[2022-08-20]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0010055	PMID:31274573	PCS		2/4			P	HPO:probinson[2023-01-23];HPO:probinson[2022-08-20]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0011483	PMID:30194805	PCS		11/12			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0007663	PMID:31274573	PCS		1/2			P	HPO:probinson[2022-08-20]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0020125	PMID:30194805	PCS		7/13			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000218	PMID:30194805	PCS		1/8			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000278	PMID:30194805	PCS		12/12			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0001763	PMID:30194805	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000594	PMID:31274573;PMID:30194805	PCS		7/8			P	HPO:probinson[2022-08-04];HPO:probinson[2023-01-23]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0001089	PMID:30194805	PCS		9/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0001166	PMID:30194805	PCS		4/5			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000494	PMID:30194805	PCS		13/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000276	PMID:30194805	PCS		6/7			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0002156	PMID:31274573	PCS		0/2			P	HPO:probinson[2022-08-20]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0001382	PMID:30194805	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0007906	PMID:30194805	PCS		6/12			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000193	PMID:30194805	PCS		1/7			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000272	PMID:30194805	PCS		7/7			P	HPO:probinson[2022-08-04];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0001083	PMID:31274573;PMID:30194805	PCS		15/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04];HPO:probinson[2022-08-20]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0011003	PMID:31274573	PCS		2/4			P	HPO:probinson[2023-01-23];HPO:probinson[2022-08-20]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0034375	PMID:31274573	PCS		4/4			P	HPO:probinson[2023-01-23];HPO:probinson[2022-09-05]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000448	OMIM:601552;PMID:30194805	PCS		23/23			P	HPO:probinson[2023-01-23];HPO:probinson[2023-01-23];HPO:skoehler[2014-08-03];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000426	PMID:30194805	PCS		13/13			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000767	PMID:30194805	PCS		1/11			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000568	OMIM:601552	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000689	PMID:30194805	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000007	PMID:24768550	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000505	PMID:24768550	PCS		1/1			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0002967	PMID:30194805	PCS		1/11			P	HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000444	OMIM:601552;PMID:30194805	PCS		23/23			P	HPO:probinson[2023-01-23];HPO:probinson[2023-01-23];HPO:skoehler[2014-08-03];HPO:probinson[2022-08-04]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000445	OMIM:601552	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:601552	Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs		HP:0000324	PMID:31274573	PCS		2/4			P	HPO:probinson[2023-01-23];HPO:probinson[2022-08-20]
OMIM:613630	Fetal encasement syndrome		HP:0009816	PMID:20961246	PCS	HP:0011461	2/2			P	HPO:probinson[2013-06-02];HPO:probinson[2022-03-12]
OMIM:613630	Fetal encasement syndrome		HP:0000085	PMID:20961246	PCS		1/2			P	HPO:probinson[2021-06-30]
OMIM:613630	Fetal encasement syndrome		HP:0011461	PMID:20961246	PCS		2/2			C	HPO:probinson[2022-03-12]
OMIM:613630	Fetal encasement syndrome		HP:0001636	PMID:20961246	PCS		1/2			P	HPO:probinson[2021-06-30]
OMIM:613630	Fetal encasement syndrome		HP:0000007	PMID:20961246	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-07-22]
OMIM:613630	Fetal encasement syndrome		HP:0001558	PMID:20961246	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:613630	Fetal encasement syndrome		HP:0001539	PMID:20961246	PCS	HP:0011461	2/2			P	HPO:probinson[2013-06-02];HPO:probinson[2021-06-30]
OMIM:613630	Fetal encasement syndrome		HP:0033984	PMID:31345061	PCS		2/2			P	HPO:probinson[2021-07-16]
OMIM:613630	Fetal encasement syndrome		HP:0011861	PMID:20961246	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:613630	Fetal encasement syndrome		HP:0000963	PMID:20961246	PCS		2/2			P	HPO:probinson[2013-06-02];HPO:probinson[2021-06-30]
OMIM:613630	Fetal encasement syndrome		HP:0000776	PMID:20961246	PCS		1/2			P	HPO:probinson[2021-06-30]
OMIM:613630	Fetal encasement syndrome		HP:0009824	PMID:20961246	PCS	HP:0011461	2/2			P	HPO:probinson[2013-06-02];HPO:probinson[2022-03-12]
OMIM:142630	Histiocytosis, progressive mucinous		HP:0040138	OMIM:142630	IEA					P	HPO:skoehler[2015-01-21]
OMIM:142630	Histiocytosis, progressive mucinous		HP:0008069	OMIM:142630	IEA					P	HPO:skoehler[2010-06-20]
OMIM:142630	Histiocytosis, progressive mucinous		HP:0000006	OMIM:142630	IEA					I	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001562	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001892	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001396	OMIM:231100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:231100	Hemochromatosis, neonatal		HP:0003577	OMIM:231100	IEA					C	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001399	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0003452	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001395	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001394	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001790	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0003281	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0011031	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0000007	OMIM:231100	IEA					I	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001404	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001943	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0001511	OMIM:231100	IEA					P	HPO:iea[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0006579	OMIM:231100	TAS					P	HPO:probinson[2009-02-17]
OMIM:231100	Hemochromatosis, neonatal		HP:0003678	OMIM:231100	IEA					C	HPO:iea[2009-02-17]
OMIM:164185	Ocular cicatricial pemphigoid		HP:0000006	OMIM:164185	IEA					I	HPO:iea[2009-02-17]
OMIM:164185	Ocular cicatricial pemphigoid		HP:0000478	OMIM:164185	IEA					P	HPO:iea[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0030269	OMIM:102200	TAS					P	HPO:probinson[2015-01-31]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0000870	OMIM:102200	TAS					P	HPO:probinson[2015-01-31]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0002893	PMID:17341560	PCS		3/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-25]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0001442	OMIM:102200	TAS					I	HPO:probinson[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0000280	OMIM:102200	TAS					P	HPO:probinson[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0011760	OMIM:102200	TAS					P	HPO:probinson[2015-01-31]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0000858	OMIM:102200	TAS					P	HPO:probinson[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0033794	PMID:17341560	PCS		2/4			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0011462	PMID:17341560	PCS		2/2			C	HPO:probinson[2022-09-25]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0000822	OMIM:102200	TAS					P	HPO:probinson[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0100829	OMIM:102200	TAS					P	HPO:skoehler[2014-06-24]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0001712	OMIM:102200	TAS					P	HPO:probinson[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0001638	OMIM:102200	TAS					P	HPO:probinson[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0000845	OMIM:102200	TAS					P	HPO:probinson[2009-02-17]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0000006	PMID:17341560	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-25]
OMIM:102200	Pituitary adenoma, growth hormone-secreting, 1		HP:0006767	OMIM:102200	TAS		20/20			P	HPO:skoehler[2017-07-13];HPO:skoehler[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0007759	PMID:12833413	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0007957	PMID:12833413	PCS		0/2			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0100864	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0100866	OMIM:271530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0000938	OMIM:271530	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0001249	PMID:12833413	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0003026	OMIM:271530	IEA				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0003301	PMID:12833413	PCS		2/2			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0003521	PMID:12833413	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0008418	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0003621	PMID:12833413	PCS		2/2			C	HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0002650	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0005004	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0000470	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0012774	PMID:12833413	PCS		2/2			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0003180	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0034770	PMID:12833413	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0002808	PMID:12833413	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0000926	PMID:12833413	PCS		2/2			P	HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0000007	OMIM:271530	IEA					I	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0000768	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0002945	PMID:12833413	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0003418	PMID:12833413	PCS		1/2			P	HPO:skoehler[2010-06-20]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0002943	PMID:12833413	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:271530	Brachyolmia type 1, Hobaek type		HP:0003952	OMIM:271530	IEA					P	HPO:iea[2009-02-17]
OMIM:186100	Syndactyly, type III		HP:0009162	OMIM:186100	TAS					P	HPO:probinson[2013-04-13]
OMIM:186100	Syndactyly, type III		HP:0011939	PMID:12457340	PCS		3/9			P	HPO:probinson[2024-07-22]
OMIM:186100	Syndactyly, type III		HP:0010705	PMID:12457340	PCS		9/9			P	HPO:probinson[2012-08-01];HPO:probinson[2024-03-08]
OMIM:186100	Syndactyly, type III		HP:0001770	PMID:12457340	PCS		0/9			P	HPO:probinson[2012-08-01];HPO:probinson[2024-03-08]
OMIM:186100	Syndactyly, type III		HP:0009237	OMIM:186100	TAS					P	HPO:probinson[2013-04-13]
OMIM:186100	Syndactyly, type III		HP:0000006	PMID:14729836	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000286	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003236	PMID:28681861	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001250	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003198	PMID:28681861	PCS		4/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001371	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0006829	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001252	OMIM:254940	IEA					P	HPO:iea[2009-02-17]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003593	OMIM:254940	IEA					C	HPO:skoehler[2018-10-08]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000162	OMIM:254940	TAS					P	HPO:skoehler[2014-06-24]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002020	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002460	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001290	OMIM:254940	IEA					P	HPO:skoehler[2018-10-08]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000518	PMID:29560417	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003701	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003306	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000278	PMID:28681861	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001249	PMID:28681861	PCS		0/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003202	OMIM:254940	IEA					P	HPO:skoehler[2018-10-08]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000252	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000494	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000175	PMID:28681861	PCS		2/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000211	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0011968	PMID:28681861	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000171	PMID:28681861	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001263	OMIM:254940	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001182	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000407	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000602	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000007	PMID:28681861	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000201	OMIM:254940	IEA					P	HPO:iea[2009-02-17]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003677	OMIM:254940	IEA					C	HPO:skoehler[2018-10-08]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0033628	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0010628	PMID:28681861	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001671	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002365	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000463	PMID:28681861	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001270	PMID:28681861	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0030319	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0012246	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001508	OMIM:254940	IEA					P	HPO:iea[2009-02-17]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0009004	PMID:28681861	PCS		8/8			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002119	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000218	PMID:28681861;PMID:29560417	PCS		7/9			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0008998	PMID:28681861;PMID:29560417	PCS		6/9			P	HPO:probinson[2022-08-14];HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000455	PMID:28681861;PMID:29560417	PCS		9/9			P	HPO:probinson[2022-08-14];HPO:skoehler[2018-10-08];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000256	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0006897	PMID:28681861	PCS		0/8			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0003621	PMID:29560417	PCS		1/1			C	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002015	PMID:29560417	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001762	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002650	PMID:28681861;PMID:29560417	PCS		5/9			P	HPO:probinson[2022-08-14];HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0030001	PMID:29560417	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002092	PMID:28681861	PCS		2/8			P	HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0002093	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0005280	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000508	PMID:28681861	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001558	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001357	OMIM:254940	TAS					P	HPO:skoehler[2017-07-13]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0001510	PMID:28681861	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000347	PMID:28681861;PMID:29560417	PCS		9/9			P	HPO:probinson[2022-08-14];HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000501	PMID:29560417	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-14]
OMIM:254940	Carey-Fineman-Ziter syndrome		HP:0000028	PMID:28681861;PMID:29560417	PCS		3/3	MALE		P	HPO:probinson[2022-08-14];HPO:skoehler[2019-04-18];HPO:probinson[2022-08-14]
OMIM:617442	Premature ovarian failure 13		HP:0003621	PMID:28175301	PCS		2/2			C	HPO:probinson[2022-08-04]
OMIM:617442	Premature ovarian failure 13		HP:0000013	PMID:28175301	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:617442	Premature ovarian failure 13		HP:0000141	PMID:28175301	PCS	HP:0011462	2/2			P	HPO:probinson[2022-08-04]
OMIM:617442	Premature ovarian failure 13		HP:0008222	PMID:28175301	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:617442	Premature ovarian failure 13		HP:0008232	PMID:28175301	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:617442	Premature ovarian failure 13		HP:0000876	PMID:28175301	PCS	HP:0003621	2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-04]
OMIM:617442	Premature ovarian failure 13		HP:0000007	PMID:28175301	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-04]
OMIM:106700	Total anomalous pulmonary venous return 1		HP:0001651	OMIM:106700	TAS					P	HPO:probinson[2022-08-08]
OMIM:106700	Total anomalous pulmonary venous return 1		HP:0002092	OMIM:106700	IEA					P	HPO:iea[2009-02-17]
OMIM:106700	Total anomalous pulmonary venous return 1		HP:0002205	OMIM:106700	IEA					P	HPO:iea[2009-02-17]
OMIM:106700	Total anomalous pulmonary venous return 1		HP:0005160	OMIM:106700	TAS					P	HPO:skoehler[2015-01-21]
OMIM:106700	Total anomalous pulmonary venous return 1		HP:0000006	OMIM:106700	IEA					I	HPO:iea[2009-02-17]
OMIM:611755	Leber congenital amaurosis 10		HP:0001250	OMIM:611755	TAS	HP:0003577	2/4		HP:0012828	P	HPO:probinson[2013-04-02]
OMIM:611755	Leber congenital amaurosis 10		HP:0000007	PMID:16909394	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-23]
OMIM:611755	Leber congenital amaurosis 10		HP:0004409	PMID:17898177	PCS					P	HPO:probinson[2013-04-02];HPO:probinson[2020-07-23]
OMIM:611755	Leber congenital amaurosis 10		HP:0000505	OMIM:611755	TAS	HP:0003577			HP:0012828	P	HPO:probinson[2013-04-02]
OMIM:600880	Budd-Chiari syndrome		HP:0003581	PMID:11001884	IEA					C	HPO:probinson[2022-03-21]
OMIM:600880	Budd-Chiari syndrome		HP:0001394	PMID:11001884	PCS		6/43			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:600880	Budd-Chiari syndrome		HP:0002639	PMID:11001884	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:600880	Budd-Chiari syndrome		HP:0000007	PMID:11001884	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-03-21]
OMIM:600880	Budd-Chiari syndrome		HP:0001402	OMIM:600880	IEA					P	HPO:iea[2009-02-17]
OMIM:227010	Ermine phenotype		HP:0001045	PMID:3055988	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:227010	Ermine phenotype		HP:0000407	PMID:3055988	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:227010	Ermine phenotype		HP:0005585	PMID:3055988	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:227010	Ermine phenotype		HP:0011364	PMID:3055988	PCS	HP:0003593	1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-08]
OMIM:227010	Ermine phenotype		HP:0008034	PMID:3055988	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:227010	Ermine phenotype		HP:0000007	OMIM:227010	IEA					I	HPO:iea[2009-02-17]
OMIM:227010	Ermine phenotype		HP:0002227	PMID:3055988	PCS		1/1			P	HPO:iea[2012-03-01];HPO:probinson[2024-03-08]
OMIM:227010	Ermine phenotype		HP:0002226	PMID:3055988	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:600670	Varicella, severe recurrent		HP:0000007	OMIM:600670	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:600670	Varicella, severe recurrent		HP:0005428	OMIM:600670	IEA					P	HPO:iea[2009-02-17]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0001397	PMID:29851065	PCS		3/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000662	PMID:29851065	PCS	HP:0011462	1/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0004322	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000089	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0001596	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0001371	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0003196	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000185	PMID:29851065	PCS		1/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0012743	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000319	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0011220	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000238	PMID:29851065	PCS		3/3			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0008278	PMID:29851065	PCS		1/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0002857	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0002714	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0008734	PMID:29851065	PCS		1/1			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000556	PMID:29851065	PCS	HP:0011462	1/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0002157	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000054	PMID:29851065	PCS		1/1			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000252	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000293	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000490	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0011344	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000609	PMID:29851065	PCS		1/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000007	PMID:29851065	PCS					I	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000648	PMID:29851065	PCS		1/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0001511	PMID:29851065	IEA	HP:0003577	4/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0000444	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0007513	PMID:29851065	PCS	HP:0003577	4/4			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0002566	PMID:29851065	PCS		1/3			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0430009	PMID:29851065	PCS		4/4			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0001974	PMID:29851065	PCS		3/3			P	HPO:probinson[2021-07-03]
OMIM:619321	Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies		HP:0008724	PMID:29851065	PCS		2/3			P	HPO:probinson[2021-07-03]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0025452	PMID:9212761	PCS	HP:0003581	4/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0025452	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0001894	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0002583	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0001061	OMIM:604416;PMID:25845478	PCS		11/11			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0011227	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0006380	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0012393	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0040310	PMID:9212761	PCS	HP:0011463	9/10			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0100658	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0033188	PMID:9212761	PCS		7/10			P	HPO:probinson[2020-10-12]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0001935	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0001433	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0002987	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0000006	PMID:9212761	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0001876	OMIM:604416	IEA					P	HPO:skoehler[2019-09-07]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0025616	PMID:9212761	PCS					P	HPO:probinson[2020-09-28]
OMIM:604416	Pyogenic sterile arthritis, pyoderma gangrenosum, and acne		HP:0001369	PMID:25845478	PCS		1/1			P	HPO:probinson[2020-09-28]
OMIM:314380	Unique green phenomenon		HP:0001417	OMIM:314380	IEA					I	HPO:iea[2009-02-17]
OMIM:314380	Unique green phenomenon		HP:0000478	OMIM:314380	IEA					P	HPO:iea[2009-02-17]
OMIM:187550	Thalassemia, beta+, silent allele		HP:0011906	OMIM:187550	TAS					P	HPO:probinson[2009-02-17]
OMIM:187550	Thalassemia, beta+, silent allele		HP:0000006	OMIM:187550	IEA					I	HPO:iea[2009-02-17]
OMIM:614163	Delayed sleep phase disorder, susceptibility to		HP:0031354	PMID:28388406	PCS					P	HPO:probinson[2022-12-04]
OMIM:614163	Delayed sleep phase disorder, susceptibility to		HP:0000006	PMID:28388406	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-04]
OMIM:604370	Breast-Ovarian cancer, familial, susceptibility to, 1		HP:0003002	PMID:11179017	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2019-07-07]
OMIM:604370	Breast-Ovarian cancer, familial, susceptibility to, 1		HP:0003596	PMID:1598904	PCS					C	HPO:probinson[2022-06-25]
OMIM:604370	Breast-Ovarian cancer, familial, susceptibility to, 1		HP:0100615	PMID:11179017	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2019-07-07]
OMIM:604370	Breast-Ovarian cancer, familial, susceptibility to, 1		HP:0001426	OMIM:604370	IEA					I	HPO:skoehler[2010-06-19]
OMIM:604370	Breast-Ovarian cancer, familial, susceptibility to, 1		HP:0000006	PMID:7545954	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2019-07-07]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000396	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000891	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000175	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000252	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0003310	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000470	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0001629	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000508	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0008551	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000767	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000007	OMIM:609654	IEA					I	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0003508	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000218	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000768	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000378	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000204	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:609654	Short stature and facioauriculothoracic malformations		HP:0000369	OMIM:609654	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0003202	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0002067	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0001260	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0001271	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0002063	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0001251	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0002380	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0000762	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0001257	OMIM:183050	IEA					P	HPO:iea[2009-02-17]
OMIM:183050	Spinocerebellar ataxia with rigidity and peripheral neuropathy		HP:0000006	OMIM:183050	IEA					I	HPO:iea[2009-02-17]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002322	PMID:11222808	PCS		1/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002067	PMID:16328510	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0003596	PMID:11222808;PMID:16328510	PCS		2/13			C	HPO:probinson[2021-02-26];HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0001332	PMID:16328510	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002362	PMID:11222808	PCS		1/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002066	PMID:11222808	PCS		1/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002063	PMID:11222808;PMID:16328510	PCS		11/13			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26];HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0025387	PMID:11222808	PCS		3/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0011462	PMID:16328510	PCS		7/10			C	HPO:probinson[2021-02-26]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0025710	PMID:11222808	PCS		1/3			C	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0001347	PMID:11222808	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002059	PMID:16328510	PCS		1/10		HP:0012825	P	HPO:probinson[2021-02-26]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0003621	PMID:16328510	PCS		2/10			C	HPO:probinson[2021-02-26]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002375	PMID:11222808	PCS		3/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0001300	PMID:11222808;PMID:16328510	PCS		13/13			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-26];HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0003487	PMID:11222808	PCS		2/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0001288	PMID:11222808	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002396	PMID:11222808	PCS		1/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0004373	PMID:11222808	PCS		1/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002174	PMID:11222808	PCS		1/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002172	PMID:11222808	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0011960	PMID:11222808	PCS		1/1			P	HPO:skoehler[2013-03-13];HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0100315	PMID:11222808	PCS		0/1			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0025708	PMID:11222808	PCS		1/3			C	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0000726	PMID:16328510	PCS		0/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-02-26]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0000007	PMID:9560156	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0002505	PMID:11222808	PCS		1/3			P	HPO:probinson[2024-03-05]
OMIM:600116	Parkinson disease, juvenile, type 2		HP:0001337	PMID:11222808;PMID:16328510	PCS		12/13			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26];HPO:probinson[2024-03-05]
OMIM:616760	Woolly hair, autosomal recessive 3		HP:0002212	PMID:26160856	PCS					P	HPO:probinson[2017-06-17]
OMIM:616760	Woolly hair, autosomal recessive 3		HP:0002213	OMIM:616760	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616760	Woolly hair, autosomal recessive 3		HP:0002209	PMID:26160856	PCS					P	HPO:probinson[2017-06-17]
OMIM:616760	Woolly hair, autosomal recessive 3		HP:0000007	PMID:26160856	PCS					I	HPO:probinson[2017-06-17]
OMIM:616760	Woolly hair, autosomal recessive 3		HP:0009886	PMID:26902920	PCS					P	HPO:probinson[2017-06-17]
OMIM:616760	Woolly hair, autosomal recessive 3		HP:0000653	PMID:26160856	PCS					P	HPO:probinson[2017-06-17]
OMIM:616760	Woolly hair, autosomal recessive 3		HP:0008070	PMID:26902920	PCS					P	HPO:probinson[2017-06-17]
OMIM:619453	Microcephaly 28, primary, autosomal recessive		HP:0000252	PMID:33199730	PCS	HP:0003577	8/8		HP:0012828	P	HPO:probinson[2021-08-20]
OMIM:619453	Microcephaly 28, primary, autosomal recessive		HP:0003577	PMID:33199730	PCS		8/8			C	HPO:probinson[2021-08-20]
OMIM:619453	Microcephaly 28, primary, autosomal recessive		HP:0000340	PMID:33199730	PCS		1/1			P	HPO:probinson[2021-08-20]
OMIM:619453	Microcephaly 28, primary, autosomal recessive		HP:0000750	PMID:33199730	PCS		4/8			P	HPO:probinson[2021-08-20]
OMIM:619453	Microcephaly 28, primary, autosomal recessive		HP:0000007	PMID:33199730	PCS					I	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:619453	Microcephaly 28, primary, autosomal recessive		HP:0001249	PMID:33199730	PCS		8/8			P	HPO:probinson[2021-08-20]
OMIM:609640	Frias syndrome		HP:0000494	OMIM:609640	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0004322	OMIM:609640	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0001263	OMIM:609640	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0000508	OMIM:609640	TAS				HP:0012832	P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0000316	OMIM:609640	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0000378	OMIM:609640	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0000520	OMIM:609640	TAS				HP:0012825	P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0000358	OMIM:609640	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0000347	OMIM:609640	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609640	Frias syndrome		HP:0000006	OMIM:609640	TAS					I	HPO:skoehler[2015-12-30]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000286	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001792	OMIM:234050	TAS					P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0002224	OMIM:234050	IEA					P	HPO:skoehler[2018-10-08]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000463	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000144	OMIM:234050	TAS					P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0002120	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0002164	OMIM:234050	TAS					P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000482	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0006829	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0003196	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001097	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0008070	OMIM:234050	TAS					P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000639	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001629	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0009886	PMID:15645389	PCS		1/1			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-04-04]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000653	OMIM:234050	IEA					P	HPO:skoehler[2018-10-08]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000278	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001249	PMID:15645389	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000252	OMIM:234050	TAS					P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0002299	PMID:15645389	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0010719	OMIM:234050	IEA					P	HPO:iea[2009-02-17]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001263	OMIM:234050	TAS		20/20			P	HPO:skoehler[2019-02-22];HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000007	PMID:15645389	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000568	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001338	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000648	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000400	OMIM:234050	TAS					P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0008404	PMID:15645389	PCS		1/1			P	HPO:probinson[2023-04-04]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001598	OMIM:234050	TAS					P	HPO:skoehler[2014-10-06]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0001510	PMID:15645389	PCS		1/1			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-04-04]
OMIM:234050	Trichothiodystrophy 4, nonphotosensitive		HP:0000685	OMIM:234050	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:613618	Chromosome 17q23.1-q23.2 duplication syndrome		HP:0001385	OMIM:613618	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613618	Chromosome 17q23.1-q23.2 duplication syndrome		HP:0001792	OMIM:613618	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613618	Chromosome 17q23.1-q23.2 duplication syndrome		HP:0001762	OMIM:613618	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613618	Chromosome 17q23.1-q23.2 duplication syndrome		HP:0002673	OMIM:613618	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613618	Chromosome 17q23.1-q23.2 duplication syndrome		HP:0008807	OMIM:613618	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613618	Chromosome 17q23.1-q23.2 duplication syndrome		HP:0002857	OMIM:613618	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613618	Chromosome 17q23.1-q23.2 duplication syndrome		HP:0000006	OMIM:613618	TAS					I	HPO:skoehler[2012-10-17]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0032051	PMID:25623524	PCS		4/7			P	HPO:nvasilevsky[2018-09-17]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0032052	PMID:25623524	PCS		2/7			P	HPO:nvasilevsky[2018-09-17]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0001250	OMIM:604364	IEA					P	HPO:skoehler[2015-01-27]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0000729	OMIM:604364	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0003829	OMIM:604364	TAS					I	HPO:skoehler[2013-07-30]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0032046	PMID:27173016	PCS					P	HPO:nvasilevsky[2018-09-17]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0032047	PMID:25623524	PCS		2/7			P	HPO:nvasilevsky[2018-09-17]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0031951	OMIM:604364	IEA		HP:0040283			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-04]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0000006	OMIM:604364	TAS					I	HPO:skoehler[2013-07-30]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0001249	OMIM:604364	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:604364	Epilepsy, familial focal, with variable foci		HP:0007206	PMID:22497611	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:191440	Ulnar hypoplasia		HP:0003022	OMIM:191440	TAS					P	HPO:skoehler[2009-02-17]
OMIM:191440	Ulnar hypoplasia		HP:0009487	OMIM:191440	TAS					P	HPO:probinson[2009-02-17]
OMIM:191440	Ulnar hypoplasia		HP:0005033	OMIM:191440	TAS					P	HPO:probinson[2009-02-17]
OMIM:191440	Ulnar hypoplasia		HP:0005011	OMIM:191440	TAS					P	HPO:probinson[2013-02-24]
OMIM:191440	Ulnar hypoplasia		HP:0006433	OMIM:191440	TAS					P	HPO:skoehler[2013-04-12]
OMIM:191440	Ulnar hypoplasia		HP:0002986	OMIM:191440	TAS	HP:0003581				P	HPO:skoehler[2009-02-17]
OMIM:191440	Ulnar hypoplasia		HP:0000006	OMIM:191440	TAS					I	HPO:probinson[2009-02-17]
OMIM:191440	Ulnar hypoplasia		HP:0002984	OMIM:191440	TAS					P	HPO:probinson[2013-04-12]
OMIM:615269	Hypogonadotropic hypogonadism 19 with or without anosmia		HP:0000044	PMID:23643382	PCS		5/5			P	HPO:probinson[2022-03-20]
OMIM:615269	Hypogonadotropic hypogonadism 19 with or without anosmia		HP:0000164	PMID:23643382	PCS		2/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-20]
OMIM:615269	Hypogonadotropic hypogonadism 19 with or without anosmia		HP:0000939	PMID:23643382	PCS		HP:0040283			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-20]
OMIM:615269	Hypogonadotropic hypogonadism 19 with or without anosmia		HP:0000365	PMID:23643382	PCS		1/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-20]
OMIM:615269	Hypogonadotropic hypogonadism 19 with or without anosmia		HP:0000938	PMID:23643382	PCS		2/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-20]
OMIM:615269	Hypogonadotropic hypogonadism 19 with or without anosmia		HP:0000006	PMID:23643382	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-20]
OMIM:612260	Immunodeficiency 68		HP:0005403	PMID:21057262	PCS		0/7			P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0002840	PMID:18669862	PCS					P	HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0006946	PMID:18669862	PCS		5/9			P	HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0001581	PMID:18669862	PCS		2/9			P	HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0040089	PMID:21057262	PCS		0/7			P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0100806	PMID:18669862	PCS		1/9			P	HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0003095	PMID:18669862	PCS		1/9			P	HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0000007	PMID:18669862	PCS					I	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0032434	PMID:31301515	PCS	HP:0003577	1/1			P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0010976	PMID:21057262;PMID:31301515	PCS		1/8			P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:612260	Immunodeficiency 68		HP:0025615	PMID:18669862	PCS		4/9			P	HPO:probinson[2020-08-31]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0000286	PMID:24913602	PCS		9/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0000365	PMID:24913602	PCS		2/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0002593	PMID:24913602	PCS		7/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0000160	PMID:24913602	PCS		6/9			P	HPO:skoehler[2014-11-26]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0000581	PMID:24913602	PCS		6/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0005183	PMID:24913602	PCS					P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0005280	PMID:24913602	PCS		8/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0012368	PMID:24913602	PCS					P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0012385	PMID:24913602	PCS		5/8			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0000939	PMID:24913602	PCS		2/9			P	HPO:probinson[2017-05-28]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0040079	PMID:24913602	PCS		8/8			P	HPO:skoehler[2014-11-26]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0008551	PMID:24913602	PCS		8/8			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0000316	PMID:24913602	PCS		9/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0001999	PMID:24913602	PCS		9/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0000007	PMID:24913602	PCS					I	HPO:skoehler[2015-12-30]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0006521	PMID:24913602	PCS					P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0001159	PMID:24913602	PCS		2/8			P	HPO:probinson[2017-05-28]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0001510	PMID:24913602	PCS		5/9			P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0001004	PMID:24913602	PCS					P	HPO:skoehler[2014-10-06]
OMIM:616006	Hennekam lymphangiectasia-lymphedema syndrome 2		HP:0002778	PMID:24913602	PCS		0/13			P	HPO:probinson[2017-05-28];HPO:probinson[2024-03-15]
OMIM:614629	Keratoconus 7		HP:0000563	OMIM:614629	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614629	Keratoconus 7		HP:0000006	OMIM:614629	TAS					I	HPO:skoehler[2012-10-17]
OMIM:615537	Reticulate acropigmentation of Kitamura		HP:0003621	PMID:23666529	PCS		7/9			C	HPO:probinson[2023-04-07]
OMIM:615537	Reticulate acropigmentation of Kitamura		HP:0011463	PMID:23666529	PCS		2/9			C	HPO:probinson[2023-04-07]
OMIM:615537	Reticulate acropigmentation of Kitamura		HP:0000006	PMID:23666529	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-07]
OMIM:615537	Reticulate acropigmentation of Kitamura		HP:0000962	PMID:23666529	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-07]
OMIM:615537	Reticulate acropigmentation of Kitamura		HP:0012733	PMID:23666529	PCS		9/9			P	HPO:probinson[2023-04-07]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000286	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0001374	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0004322	PMID:24726473	PCS		9/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-11]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0100490	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0003199	OMIM:114300	TAS					P	HPO:skoehler[2015-12-30]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0001193	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0002938	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0001845	OMIM:114300	TAS					P	HPO:skoehler[2014-08-03]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000954	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000218	OMIM:114300	TAS					P	HPO:skoehler[2014-08-03]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0200021	OMIM:114300	TAS		20/20			P	HPO:probinson[2023-03-11];HPO:probinson[2023-03-11];HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0009803	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0002751	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000176	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000175	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0002650	PMID:24726473	PCS		6/15			P	HPO:probinson[2023-03-11]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0001762	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000193	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0005684	OMIM:114300	IEA					P	HPO:skoehler[2015-01-21]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0001263	OMIM:114300	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000470	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0010554	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0003184	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0006380	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0007099	PMID:24726473	PCS		3/12			P	HPO:probinson[2023-03-11]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000508	PMID:24726473	PCS		5/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-11]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000602	PMID:24726473	PCS		2/14			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-03-11]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000767	OMIM:114300	TAS					P	HPO:skoehler[2014-08-03]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0002804	OMIM:114300	IEA					P	HPO:skoehler[2015-01-19]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0001836	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0002944	OMIM:114300	TAS					P	HPO:skoehler[2014-08-03]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000006	PMID:24726473	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-11]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000028	OMIM:114300	IEA					P	HPO:iea[2009-02-17]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000347	PMID:24726473	PCS		11/14			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-03-11]
OMIM:114300	Arthrogryposis, distal, type 3		HP:0000324	OMIM:114300	TAS				HP:0012825	P	HPO:skoehler[2014-08-03]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0000252	PMID:15070707	PCS		3/7			P	HPO:probinson[2013-03-24]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0002023	PMID:15070707	PCS		2/7			P	HPO:probinson[2013-03-24]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0006727	PMID:15070707	PCS		1/7			P	HPO:probinson[2013-03-24]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0004322	OMIM:605724	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0001508	PMID:15070707	PCS		5/7			P	HPO:probinson[2013-03-24]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0003221	PMID:15070707	PCS					P	HPO:probinson[2013-01-09]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0000957	PMID:15070707	PCS		4/7			P	HPO:probinson[2013-03-24]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0004808	PMID:15070707	PCS		5/7			P	HPO:probinson[2013-03-24]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0000007	PMID:15070707	PCS					I	HPO:probinson[2013-12-14]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0001511	PMID:15070707	PCS		7/7			P	HPO:probinson[2013-03-24]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0005528	OMIM:605724	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605724	Fanconi anemia, complementation group D1		HP:0009778	PMID:15070707	PCS		1/7			P	HPO:probinson[2013-03-24]
OMIM:267430	Renal tubular dysgenesis		HP:0001562	OMIM:267430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267430	Renal tubular dysgenesis		HP:0000252	OMIM:267430	IEA					P	HPO:iea[2009-02-17]
OMIM:267430	Renal tubular dysgenesis		HP:0000079	OMIM:267430	IEA					P	HPO:iea[2009-02-17]
OMIM:267430	Renal tubular dysgenesis		HP:0002089	OMIM:267430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267430	Renal tubular dysgenesis		HP:0008660	OMIM:267430	TAS					P	HPO:skoehler[2014-03-24]
OMIM:267430	Renal tubular dysgenesis		HP:0000007	OMIM:267430	IEA					I	HPO:iea[2009-02-17]
OMIM:267430	Renal tubular dysgenesis		HP:0004492	OMIM:267430	IEA					P	HPO:iea[2009-02-17]
OMIM:267430	Renal tubular dysgenesis		HP:0002009	OMIM:267430	IEA					P	HPO:iea[2009-02-17]
OMIM:267430	Renal tubular dysgenesis		HP:0002093	OMIM:267430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267430	Renal tubular dysgenesis		HP:0002615	OMIM:267430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267430	Renal tubular dysgenesis		HP:0100519	OMIM:267430	TAS					P	HPO:skoehler[2012-10-17]
OMIM:242840	Vici syndrome		HP:0000286	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0003236	PMID:25331754	PCS		7/7			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0010803	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001250	PMID:25331754	PCS		13/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0003198	PMID:25331754	PCS		9/27			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000161	PMID:25331754	PCS		4/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001252	PMID:25331754	PCS		17/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001010	PMID:25331754	PCS		27/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0003593	PMID:25331754	PCS		1/1			C	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000639	PMID:25331754	PCS		10/27			P	HPO:skoehler[2013-03-08];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000518	PMID:25331754	PCS		22/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0011220	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0012471	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000519	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0000316	PMID:25331754	PCS		2/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001888	PMID:25331754	PCS		3/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0008897	PMID:25331754	PCS		12/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0007401	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0002533	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0001644	OMIM:242840	TAS					P	HPO:skoehler[2013-03-08]
OMIM:242840	Vici syndrome		HP:0004315	PMID:25331754	PCS		5/27			P	HPO:probinson[2012-05-06];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000252	PMID:25331754	PCS		14/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000175	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0001022	OMIM:242840	TAS					P	HPO:skoehler[2013-01-22]
OMIM:242840	Vici syndrome		HP:0003244	OMIM:242840	TAS					P	HPO:probinson[2012-04-26]
OMIM:242840	Vici syndrome		HP:0001263	PMID:25331754	PCS		27/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0010636	OMIM:242840	IEA					P	HPO:skoehler[2010-06-20]
OMIM:242840	Vici syndrome		HP:0000407	OMIM:242840	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:242840	Vici syndrome		HP:0009099	PMID:25331754	PCS		4/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000007	PMID:25331754	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000601	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0005419	OMIM:242840	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000369	PMID:25331754	PCS		2/27			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000204	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0000325	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000445	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000341	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0003577	OMIM:242840	TAS					C	HPO:skoehler[2012-10-17]
OMIM:242840	Vici syndrome		HP:0005599	PMID:25331754	PCS		26/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000343	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001274	PMID:25331754	PCS		27/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0002282	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0001270	PMID:25331754	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001508	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0002718	PMID:25331754	PCS					P	HPO:probinson[2012-04-26];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001107	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0000777	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0000218	PMID:25331754	PCS		10/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001104	PMID:25331754	PCS		2/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001941	OMIM:242840	TAS					P	HPO:skoehler[2013-01-22]
OMIM:242840	Vici syndrome		HP:0001320	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0005403	PMID:25331754	PCS		3/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0002015	PMID:25331754	PCS		4/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001882	PMID:25331754	PCS		3/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0005280	PMID:25331754	PCS		2/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0002728	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0000508	PMID:25331754	PCS		2/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001712	OMIM:242840	TAS					P	HPO:skoehler[2012-10-17]
OMIM:242840	Vici syndrome		HP:0007894	PMID:25331754	PCS		18/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0001635	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0001638	PMID:25331754	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0004429	PMID:25331754	PCS					P	HPO:probinson[2012-04-26];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0002205	PMID:25331754	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0008348	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0002965	OMIM:242840	IEA					P	HPO:iea[2009-02-17]
OMIM:242840	Vici syndrome		HP:0001631	PMID:25331754	PCS		2/27			P	HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0002841	PMID:25331754	PCS					P	HPO:probinson[2012-04-26];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0000347	PMID:25331754	PCS		10/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:242840	Vici syndrome		HP:0002721	OMIM:242840	TAS					P	HPO:probinson[2012-04-26]
OMIM:242840	Vici syndrome		HP:0001875	PMID:25331754	PCS		1/27			P	HPO:probinson[2022-11-08]
OMIM:600884	Cardiomyopathy, dilated, 1B		HP:0006670	OMIM:600884	IEA					P	HPO:iea[2009-02-17]
OMIM:600884	Cardiomyopathy, dilated, 1B		HP:0002617	OMIM:600884	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600884	Cardiomyopathy, dilated, 1B		HP:0001635	OMIM:600884	IEA					P	HPO:skoehler[2019-02-22]
OMIM:600884	Cardiomyopathy, dilated, 1B		HP:0004308	OMIM:600884	IEA					P	HPO:iea[2009-02-17]
OMIM:600884	Cardiomyopathy, dilated, 1B		HP:0000006	PMID:7573045	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-07-03]
OMIM:600884	Cardiomyopathy, dilated, 1B		HP:0001644	PMID:7573045	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:617320	Ichthyosis, congenital, autosomal recessive 12		HP:0000007	PMID:27494380	PCS					I	HPO:probinson[2017-06-16]
OMIM:617320	Ichthyosis, congenital, autosomal recessive 12		HP:0040190	PMID:27494380	PCS					P	HPO:probinson[2017-06-16]
OMIM:618013	Deafness, autosomal recessive 109		HP:0011380	PMID:29107558	PCS		2/2			P	HPO:probinson[2019-06-13]
OMIM:618013	Deafness, autosomal recessive 109		HP:0000007	PMID:29107558	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:618013	Deafness, autosomal recessive 109		HP:0008555	PMID:29107558	IEA		0/2			P	HPO:probinson[2019-06-13];HPO:probinson[2024-03-15]
OMIM:618013	Deafness, autosomal recessive 109		HP:0008527	PMID:29107558	PCS	HP:0003577	2/2		HP:0012829	P	HPO:probinson[2019-06-13]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0000253	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001298	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0003676	OMIM:610329	TAS					C	HPO:skoehler[2015-12-30]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001332	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0002079	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0200149	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001252	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0012448	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001290	OMIM:610329	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0011344	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0003819	PMID:16845400	PCS					C	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0000639	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0000007	PMID:16845400	PCS					I	HPO:probinson[2013-01-09]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0009710	OMIM:610329	IEA					P	HPO:skoehler[2019-04-18]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001257	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0002514	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001873	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001433	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0002910	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0002500	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610329	Aicardi-Goutieres syndrome 3		HP:0001347	OMIM:610329	TAS					P	HPO:skoehler[2015-08-16]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0002883	PMID:31883641	PCS		1/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0004897	PMID:31883641	PCS	HP:0003593	2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0007418	PMID:31883641	PCS		2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0003236	PMID:31883641	PCS		1/1			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0002045	PMID:31883641	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001662	PMID:31883641	PCS	HP:0011461	2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0005301	PMID:31883641	PCS	HP:0003577	1/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001085	PMID:31883641	PCS		1/1		HP:0012832	P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0011726	PMID:31883641	PCS	HP:0003577	1/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001252	PMID:31883641	PCS		2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001081	PMID:31883641	PCS		1/1			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001270	PMID:31883641	PCS		1/1			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001629	PMID:31883641	PCS	HP:0003577	1/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001639	PMID:31883641	PCS		2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001518	PMID:31883641	PCS		1/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001928	PMID:31883641	PCS		1/1			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0000007	PMID:31883641	PCS					I	HPO:probinson[2020-05-09];HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0008872	PMID:31883641	PCS		2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001511	PMID:31883641	PCS		1/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001324	PMID:31883641	PCS		2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001698	PMID:31883641	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001895	PMID:31883641	PCS		1/1			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0001873	PMID:31883641	PCS		2/2			P	HPO:probinson[2020-05-09]
OMIM:618775	Mitochondrial complex III deficiency, nuclear type 10		HP:0003128	PMID:31883641	PCS		2/2			P	HPO:probinson[2020-05-09]
OMIM:601224	Potocki-Shaffer syndrome		HP:0002762	PMID:8644736	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000286	PMID:8644736	PCS		4/9			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0001156	PMID:15852040	PCS		5/8			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0001250	PMID:8644736	PCS		2/11			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000262	OMIM:601224	TAS					P	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0005650	OMIM:601224	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0001252	PMID:8644736	PCS		5/9			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0003196	PMID:8644736	PCS					P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000954	PMID:8644736	PCS		5/6			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000337	PMID:8644736	PCS					P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0002714	PMID:15852040	PCS		8/9			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0004439	PMID:8644736	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0001466	OMIM:601224	TAS					I	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0001249	PMID:8644736	PCS		7/10			P	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0002697	PMID:8644736	PCS		9/11			P	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000054	PMID:8644736	PCS		5/6			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000494	PMID:8644736	PCS					P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000431	PMID:8644736	PCS					P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000430	PMID:8644736	PCS					P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000506	PMID:8644736	PCS		4/9			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000348	PMID:8644736	PCS					P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0002645	PMID:8644736	PCS		3/6			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000322	PMID:15852040	PCS		6/9			P	HPO:iea[2010-09-15]
OMIM:601224	Potocki-Shaffer syndrome		HP:0000248	PMID:8644736	PCS		6/9			P	HPO:iea[2009-02-17]
OMIM:601224	Potocki-Shaffer syndrome		HP:0005338	PMID:15852040	PCS		6/9			P	HPO:iea[2010-09-15]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0001562	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0002023	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0002089	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0002650	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000068	OMIM:271520	TAS					P	HPO:probinson[2014-01-18]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000023	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0001195	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000042	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000151	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000470	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0003250	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0003270	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000902	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0002937	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0002948	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000316	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000921	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0002946	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000007	OMIM:271520	IEA					I	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000268	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0003305	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000883	OMIM:271520	TAS					P	HPO:probinson[2012-05-27]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000773	OMIM:271520	TAS					P	HPO:probinson[2012-05-27]
OMIM:271520	Spondylocostal dysostosis with anal atresia and urogenital anomalies		HP:0000126	OMIM:271520	IEA					P	HPO:iea[2009-02-17]
OMIM:604348	Advanced sleep phase syndrome, familial, 1		HP:0006979	PMID:10470086	PCS	HP:0003621	HP:0040281			P	HPO:iea[2010-04-27]
OMIM:604348	Advanced sleep phase syndrome, familial, 1		HP:0000716	OMIM:604348	TAS					P	HPO:skoehler[2015-12-30]
OMIM:604348	Advanced sleep phase syndrome, familial, 1		HP:0031873	OMIM:604348	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604348	Advanced sleep phase syndrome, familial, 1		HP:0000006	OMIM:604348	PCS					I	HPO:iea[2010-04-27]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0002366	OMIM:607641	IEA					P	HPO:iea[2009-02-17]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0030237	PMID:12627231	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0009130	PMID:12627231	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0003693	PMID:12627231	PCS					P	HPO:probinson[2012-04-26];HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0007340	OMIM:607641	IEA					P	HPO:iea[2009-02-17]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0003581	PMID:12627231	PCS					C	HPO:probinson[2012-04-26];HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0002460	PMID:12627231	PCS					P	HPO:probinson[2012-04-26];HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0001605	PMID:12627231	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0030319	PMID:12627231	PCS					P	HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0003677	PMID:12627231	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:607641	Neuronopathy, distal hereditary motor, type VIIB		HP:0000006	PMID:12627231	PCS					I	HPO:probinson[2012-04-26];HPO:probinson[2023-02-10]
OMIM:223500	Dwarfism, low-birth-weight type, with unresponsiveness to growth hormone		HP:0003510	OMIM:223500	IEA					P	HPO:iea[2009-02-17]
OMIM:223500	Dwarfism, low-birth-weight type, with unresponsiveness to growth hormone		HP:0000365	OMIM:223500	IEA					P	HPO:iea[2009-02-17]
OMIM:223500	Dwarfism, low-birth-weight type, with unresponsiveness to growth hormone		HP:0001419	OMIM:223500	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:223500	Dwarfism, low-birth-weight type, with unresponsiveness to growth hormone		HP:0000007	OMIM:223500	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:223500	Dwarfism, low-birth-weight type, with unresponsiveness to growth hormone		HP:0001943	OMIM:223500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:223500	Dwarfism, low-birth-weight type, with unresponsiveness to growth hormone		HP:0001511	OMIM:223500	IEA					P	HPO:iea[2009-02-17]
OMIM:223500	Dwarfism, low-birth-weight type, with unresponsiveness to growth hormone		HP:0001249	OMIM:223500	IEA					P	HPO:iea[2009-02-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0100336	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0002389	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0001344	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0000914	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0000470	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0000767	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0000007	PMID:35614220	PCS					I	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0012368	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0002943	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616994	Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		HP:0000369	PMID:35614220	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0000384	PMID:25434003	PCS		8/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0003577	PMID:25434003	PCS					C	HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000365	PMID:25434003	PCS		10/14			P	HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000089	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0004322	PMID:25434003	PCS		2/14			P	HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000122	PMID:25434003	PCS		1/14			P	HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000023	PMID:25434003	PCS		2/14			P	HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000160	PMID:25434003	PCS		1/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0200138	OMIM:608572	TAS					P	HPO:skoehler[2013-06-12]
OMIM:608572	Burn-Mckeown syndrome		HP:0000581	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0012745	PMID:25434003	PCS		14/14			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0001629	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0000316	PMID:25434003	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000338	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0008872	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0000411	PMID:25434003	PCS		10/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000652	PMID:25434003	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000175	PMID:25434003	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000453	PMID:25434003	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000233	PMID:25434003	PCS		8/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000430	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0000193	PMID:25434003	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0004691	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0000426	PMID:25434003	PCS		13/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000007	PMID:25434003	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000405	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0001631	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0000322	PMID:25434003	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000204	PMID:25434003	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0000303	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:608572	Burn-Mckeown syndrome		HP:0000347	PMID:25434003	PCS		9/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:608572	Burn-Mckeown syndrome		HP:0004502	OMIM:608572	IEA					P	HPO:iea[2009-02-17]
OMIM:254950	Myopathy, granulovacuolar lobular, with electrical myotonia		HP:0003202	OMIM:254950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254950	Myopathy, granulovacuolar lobular, with electrical myotonia		HP:0002486	OMIM:254950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254950	Myopathy, granulovacuolar lobular, with electrical myotonia		HP:0001939	OMIM:254950	IEA					P	HPO:iea[2009-02-17]
OMIM:254950	Myopathy, granulovacuolar lobular, with electrical myotonia		HP:0000007	OMIM:254950	IEA					I	HPO:iea[2009-02-17]
OMIM:254950	Myopathy, granulovacuolar lobular, with electrical myotonia		HP:0001324	OMIM:254950	IEA					P	HPO:iea[2009-02-17]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0004325	PMID:28343629	PCS		6/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000365	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0002540	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0004322	PMID:28343629	PCS		7/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001371	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001250	PMID:28343629	PCS		12/12			P	HPO:skoehler[2018-10-08];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001290	PMID:28343629	PCS		9/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001845	PMID:28343629	PCS		3/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000637	PMID:28343629	PCS		6/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000278	PMID:28343629	PCS		4/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0200021	PMID:28343629	PCS		3/12			P	HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0005469	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0002553	PMID:28343629	PCS		3/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000494	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000252	PMID:28343629	PCS	HP:0003593	9/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0002510	PMID:28343629	PCS		2/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0002079	PMID:28343629	PCS		3/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0011968	PMID:28343629	PCS		9/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001263	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0002194	PMID:28343629	PCS	HP:0003593	9/12			P	HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001182	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000729	PMID:28343629	PCS		3/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000007	PMID:28343629	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000527	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000400	PMID:28343629	PCS		7/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000960	PMID:28343629	PCS		2/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000248	PMID:28343629	PCS		1/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000369	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001276	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000343	PMID:28343629	PCS		7/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001508	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001629	PMID:28343629	PCS		2/6			P	HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0012450	PMID:28343629	PCS		2/12			P	HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000219	PMID:28343629	PCS		6/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0002119	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000218	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000411	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000377	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0002650	PMID:28343629	PCS		5/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001762	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000431	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000750	PMID:28343629	PCS		9/12			P	HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000276	OMIM:617452	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000470	PMID:28343629	PCS		3/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0011304	PMID:28343629	PCS		6/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000426	PMID:28343629	PCS		5/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001511	PMID:28343629	PCS	HP:0030674	7/12			P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0001631	PMID:28343629	PCS		3/6			P	HP:probinson[2019-05-03]
OMIM:617452	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies		HP:0000028	PMID:28343629	PCS					P	HPO:skoehler[2017-07-13];HP:probinson[2019-05-03]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000483	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000365	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001530	OMIM:150230	TAS					P	HPO:probinson[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001250	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001252	PMID:23913778	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002020	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0003593	PMID:23913778	PCS		1/4			C	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0010049	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000918	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001808	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0100246	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0010291	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000958	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0011463	PMID:23913778	PCS		3/4			C	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000954	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001647	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001249	PMID:23913778	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0003764	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000252	PMID:23913778	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0005743	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000574	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000771	PMID:23913778	PCS		3/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002673	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0010714	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001382	PMID:23913778	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001260	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000490	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001263	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002829	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0007595	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000448	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000767	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001658	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000403	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002944	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000966	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0004209	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002788	PMID:23913778	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000400	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0008689	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000369	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000006	PMID:23913778	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000324	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0005039	PMID:23913778	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000023	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002002	PMID:23913778	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0030431	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0003691	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0005231	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001270	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0008070	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000616	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000938	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0010230	PMID:23913778	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0030043	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000975	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000414	PMID:23913778	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000219	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0006532	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002678	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000411	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001269	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001667	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000896	PMID:23913778	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000577	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000973	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000076	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000670	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000431	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002650	OMIM:150230	IEA		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000750	OMIM:150230	IEA					P	HPO:iea[2009-02-17]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002013	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002373	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002293	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0010773	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0012159	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000508	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002209	PMID:23913778	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0030010	OMIM:150230	TAS					P	HPO:skoehler[2014-09-21]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0430028	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002408	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001159	OMIM:150230	IEA					P	HPO:skoehler[2010-06-18]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0002205	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001357	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0004626	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0001510	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000545	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000347	PMID:23913778	PCS		1/4			P	HPO:probinson[2022-04-19]
OMIM:150230	Trichorhinophalangeal syndrome, type II		HP:0000303	PMID:23913778	PCS		2/4			P	HPO:probinson[2022-04-19]
OMIM:618761	Catifa syndrome		HP:0000286	PMID:31932796	PCS		4/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000692	PMID:31932796	PCS		4/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000175	PMID:31932796	PCS		3/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000684	PMID:31932796	PCS		3/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000486	PMID:31932796	PCS		5/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000343	PMID:31932796	PCS		3/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000023	PMID:31932796	PCS		2/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0001288	PMID:31932796	PCS		8/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000276	PMID:31932796	PCS		6/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000463	PMID:31932796	PCS		5/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0002099	PMID:31932796	PCS		5/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0001263	PMID:27878435;PMID:31932796	PCS		10/10			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0410030	PMID:31932796	PCS		5/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0040196	PMID:31932796	PCS		4/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0012385	PMID:31932796	PCS		1/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0011094	PMID:31932796	PCS		2/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000519	PMID:27878435	PCS	HP:0003577	2/2			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000519	PMID:31932796	PCS		7/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0008551	PMID:31932796	PCS		5/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000646	PMID:31932796	PCS		3/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0000007	PMID:27878435	PCS					I	HPO:probinson[2020-04-23];HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0007018	PMID:31932796	PCS		7/8			P	HPO:probinson[2020-04-23]
OMIM:618761	Catifa syndrome		HP:0001249	PMID:31932796	PCS		8/8			P	HPO:probinson[2020-04-23]
OMIM:601230	Dermatitis herpetiformis, familial		HP:0000989	PMID:24068131	PCS					P	HPO:skoehler[2015-05-03]
OMIM:601230	Dermatitis herpetiformis, familial		HP:0000006	OMIM:601230	TAS					I	HPO:iea[2009-02-17]
OMIM:182410	Sneddon syndrome		HP:0010628	OMIM:182410	IEA					P	HPO:skoehler[2010-06-18]
OMIM:182410	Sneddon syndrome		HP:0002301	PMID:18474464	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0003676	OMIM:182410	IEA					C	HPO:skoehler[2010-06-19]
OMIM:182410	Sneddon syndrome		HP:0001297	PMID:31652311	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:182410	Sneddon syndrome		HP:0001250	OMIM:182410	IEA					P	HPO:skoehler[2010-06-18]
OMIM:182410	Sneddon syndrome		HP:0002140	PMID:12804991	PCS		2/4			P	HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0001075	PMID:12804991	PCS		3/4			P	HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0003593	PMID:31652311	PCS		1/1			C	HPO:probinson[2022-03-13]
OMIM:182410	Sneddon syndrome		HP:0033505	PMID:12804991	PCS		4/4			P	HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0001647	PMID:31652311	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:182410	Sneddon syndrome		HP:0001888	PMID:31652311	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:182410	Sneddon syndrome		HP:0002315	PMID:18474464	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0003745	OMIM:182410	IEA					I	HPO:skoehler[2010-06-19]
OMIM:182410	Sneddon syndrome		HP:0001268	OMIM:182410	IEA					P	HPO:skoehler[2010-06-18]
OMIM:182410	Sneddon syndrome		HP:0001342	PMID:12804991	PCS		1/4			P	HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0002850	PMID:31652311	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:182410	Sneddon syndrome		HP:0006937	PMID:31652311	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:182410	Sneddon syndrome		HP:0001260	PMID:18474464	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0033832	PMID:31652311	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:182410	Sneddon syndrome		HP:0033260	PMID:18474464	PCS		3/3			P	HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0000965	OMIM:182410	IEA					P	HPO:iea[2009-02-17]
OMIM:182410	Sneddon syndrome		HP:0000822	PMID:12804991	PCS		3/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0000007	PMID:12804991	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-04-29]
OMIM:182410	Sneddon syndrome		HP:0003613	OMIM:182410	IEA					P	HPO:iea[2009-02-17]
OMIM:182410	Sneddon syndrome		HP:0001337	OMIM:182410	IEA					P	HPO:skoehler[2010-06-18]
OMIM:619319	Lymphatic malformation 9		HP:0003550	PMID:26855770	PCS		2/2			P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:619319	Lymphatic malformation 9		HP:0033986	PMID:26855770	PCS		1/2			P	HPO:probinson[2021-07-16]
OMIM:619319	Lymphatic malformation 9		HP:0000006	PMID:26855770	PCS					I	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0003324	PMID:17878207	PCS		1/1			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0003236	PMID:17878207;PMID:19299310	PCS		2/2			P	HPO:probinson[2022-03-27];HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0011463	PMID:17878207	PCS		1/1			C	HPO:probinson[2022-03-27]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0001252	OMIM:613152	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0003560	PMID:17878207	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0003593	PMID:19299310	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0000007	PMID:19299310	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0001270	PMID:17878207	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:613152	Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development), type B, 4		HP:0002500	PMID:17878207	PCS		1/1			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:227000	Erythema of acral regions		HP:0000164	OMIM:227000	IEA					P	HPO:iea[2009-02-17]
OMIM:227000	Erythema of acral regions		HP:0001762	OMIM:227000	IEA					P	HPO:iea[2009-02-17]
OMIM:227000	Erythema of acral regions		HP:0000007	OMIM:227000	IEA					I	HPO:iea[2009-02-17]
OMIM:227000	Erythema of acral regions		HP:0010783	OMIM:227000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:615523	Corneal dystrophy, fuchs endothelial, 8		HP:0001131	PMID:24094747	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-11-21]
OMIM:615523	Corneal dystrophy, fuchs endothelial, 8		HP:0003581	PMID:24094747	PCS					C	HPO:probinson[2022-11-21]
OMIM:615523	Corneal dystrophy, fuchs endothelial, 8		HP:0012038	PMID:24094747	PCS		12/12			P	HPO:probinson[2022-11-21]
OMIM:615523	Corneal dystrophy, fuchs endothelial, 8		HP:0000006	PMID:24094747	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-21]
OMIM:609122	Aneurysm, intracranial berry, 3		HP:0007029	OMIM:609122	TAS					P	HPO:probinson[2017-06-23]
OMIM:609122	Aneurysm, intracranial berry, 3		HP:0000006	OMIM:609122	TAS					I	HPO:probinson[2017-06-23]
OMIM:212093	Cardiac valvular defect, developmental		HP:0003577	PMID:27799408	PCS		6/6			C	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0004762	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0000023	OMIM:212093	IEA					P	HPO:iea[2009-02-17]
OMIM:212093	Cardiac valvular defect, developmental		HP:0011555	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0010446	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0011662	PMID:27799408	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001629	PMID:27799408	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0031295	PMID:27799408	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001789	OMIM:212093	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001704	OMIM:212093	TAS					P	HPO:skoehler[2017-07-13]
OMIM:212093	Cardiac valvular defect, developmental		HP:0004935	PMID:27799408	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001642	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0000072	OMIM:212093	IEA					P	HPO:iea[2009-02-17]
OMIM:212093	Cardiac valvular defect, developmental		HP:0034348	PMID:27799408	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0031632	OMIM:212093	TAS					P	HPO:skoehler[2017-07-13]
OMIM:212093	Cardiac valvular defect, developmental		HP:0005180	OMIM:212093	IEA					P	HPO:iea[2009-02-17]
OMIM:212093	Cardiac valvular defect, developmental		HP:0011623	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0011591	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0034350	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0000969	OMIM:212093	IEA					P	HPO:skoehler[2010-06-20]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001718	OMIM:212093	IEA					P	HPO:iea[2009-02-17]
OMIM:212093	Cardiac valvular defect, developmental		HP:0000007	PMID:27799408	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0000961	PMID:27799408	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001631	PMID:27799408	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001653	PMID:27799408	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:212093	Cardiac valvular defect, developmental		HP:0008722	OMIM:212093	IEA					P	HPO:iea[2009-02-17]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001634	OMIM:212093	TAS					P	HPO:skoehler[2017-07-13]
OMIM:212093	Cardiac valvular defect, developmental		HP:0000126	OMIM:212093	IEA					P	HPO:iea[2009-02-17]
OMIM:212093	Cardiac valvular defect, developmental		HP:0001655	OMIM:212093	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0003774	PMID:24676634	PCS		9/18			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-24]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0000100	PMID:24676634	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-24]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0000089	PMID:24676634	PCS		1/18			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-24]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0000097	PMID:24676634	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-24]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0003581	PMID:24676634	PCS					C	HPO:probinson[2022-09-24]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0003829	OMIM:616002	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0000093	PMID:24676634	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-24]
OMIM:616002	Focal segmental glomerulosclerosis 7		HP:0000006	PMID:24676634	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-24]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001771	PMID:37303127	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0008209	PMID:37303127	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003233	PMID:37843397;PMID:37303127;PMID:17250669;PMID:11344241	PCS		70/119			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000287	PMID:17250669	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0004322	PMID:37303127;PMID:17250669	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003198	PMID:17250669;PMID:11344241	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003074	PMID:37303127;PMID:17250669	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0009064	PMID:37843397;PMID:37303127;PMID:11344241	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0100324	PMID:17250669	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0011463	PMID:37303127;PMID:17250669	PCS		2/9			C	ORCID:0000-0002-0736-9199[2024-11-08];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0012592	PMID:37303127	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0011462	PMID:37303127;PMID:17250669	PCS		2/9			C	ORCID:0000-0002-0736-9199[2024-11-08];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000956	PMID:17250669;PMID:11344241	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0040217	PMID:37843397;PMID:37303127;PMID:17250669;PMID:11344241	PCS		79/110			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001324	PMID:17250669;PMID:11344241	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000311	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001007	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000831	PMID:17250669	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0005328	PMID:37303127;PMID:17250669	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001644	PMID:37843397;PMID:37303127	PCS		3/101			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0031956	PMID:37303127	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0002155	PMID:37843397;PMID:37303127;PMID:17250669;PMID:11344241	PCS		79/118			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003124	PMID:37843397;PMID:28450900;PMID:37303127;PMID:17250669	PCS		55/125			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:nvasilevsky[2019-03-12]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0030781	PMID:37303127	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003560	PMID:37303127	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0005181	PMID:37843397	PCS		9/115			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0012100	PMID:37303127	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0007394	PMID:17250669	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0012185	PMID:11344241	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001735	OMIM:151660	TAS		HP:0040282			P	HPO:probinson[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001657	PMID:37303127	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003758	OMIM:151660	TAS					P	HPO:probinson[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003635	PMID:37843397;PMID:17250669;PMID:11344241	PCS		121/121			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003712	PMID:17250669;PMID:11344241	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0008887	OMIM:151660	TAS					P	HPO:probinson[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001015	OMIM:151660;PMID:17250669	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000520	PMID:17250669	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0005978	PMID:37843397;PMID:37303127;PMID:17250669;PMID:11344241	PCS		89/122			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0002621	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000006	OMIM:151660	IEA					I	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000842	PMID:37303127	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001733	PMID:37843397;PMID:17250669	PCS		18/117			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0002149	PMID:37303127	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001397	PMID:37843397;PMID:37303127	PCS		87/108			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001596	PMID:17250669	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0002486	PMID:37303127	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0005110	PMID:37303127	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0002240	PMID:11344241	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001070	PMID:17250669	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0031964	PMID:37303127	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0012645	OMIM:151660	TAS					P	HPO:skoehler[2014-02-06]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000939	PMID:37303127	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001508	PMID:17250669	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0009002	PMID:37843397	PCS		108/115			P	HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000855	PMID:37303127	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0008993	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0009125	PMID:37843397;PMID:37303127;PMID:17250669;PMID:11344241	PCS		121/121			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:probinson[2009-02-17];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001744	PMID:11344241	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003326	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003621	PMID:37303127;PMID:17250669	PCS		5/9			C	ORCID:0000-0002-0736-9199[2024-11-08];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0002650	PMID:37303127	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0008739	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000991	PMID:17250669;PMID:11344241	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-11-08];HPO:iea[2009-02-17];HPO:probinson[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003584	PMID:37303127	PCS		1/6			C	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003581	PMID:17250669	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003141	PMID:37843397;PMID:37303127;PMID:17250669	PCS		25/110			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0033477	PMID:11344241	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0011227	PMID:37303127	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0031185	PMID:37303127	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0003738	PMID:11344241	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000822	PMID:17250669	PCS	HP:0003584	1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001635	PMID:37303127	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001638	PMID:37303127;PMID:17250669	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0008985	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0025502	PMID:37843397;PMID:17250669	PCS		42/102			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000147	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001678	PMID:37843397;PMID:17250669	PCS		2/118			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000468	OMIM:151660	IEA					P	HPO:iea[2009-02-17]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0000347	PMID:17250669	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001513	PMID:37843397;PMID:17250669;PMID:11344241	PCS		21/103			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:151660	Lipodystrophy, familial partial, type 2		HP:0001952	PMID:37303127	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-08]
OMIM:614615	Joubert syndrome 17		HP:0002883	PMID:22425360	PCS		8/10		HP:0025303	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0100259	PMID:22425360	PCS		1/10			P	HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0011939	PMID:22425360	PCS		1/10			P	HPO:probinson[2024-07-22]
OMIM:614615	Joubert syndrome 17		HP:0012210	PMID:22425360	PCS		0/7			P	HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0100258	PMID:22425360	PCS		1/10			P	HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0001263	PMID:22425360	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0001251	OMIM:614615	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614615	Joubert syndrome 17		HP:0003593	PMID:22425360	PCS					C	HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0000657	PMID:22425360	PCS		9/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0000007	PMID:22425360	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0002419	PMID:22425360	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-13]
OMIM:614615	Joubert syndrome 17		HP:0000479	PMID:22425360	PCS		0/10			P	HPO:probinson[2022-10-13]
OMIM:314390	VACTERL association, X-linked		HP:0000068	OMIM:314390	IEA					P	HPO:iea[2009-02-17]
OMIM:314390	VACTERL association, X-linked		HP:0002023	PMID:20452998	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0002089	PMID:20452998	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0001651	PMID:20452998	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0005792	OMIM:314390	IEA					P	HPO:iea[2009-02-17]
OMIM:314390	VACTERL association, X-linked		HP:0010963	PMID:20452998	PCS	HP:0034197	1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0008750	PMID:20452998	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0001669	OMIM:314390	TAS					P	HPO:skoehler[2015-12-30]
OMIM:314390	VACTERL association, X-linked		HP:0000238	OMIM:314390	IEA					P	HPO:iea[2009-02-17]
OMIM:314390	VACTERL association, X-linked		HP:0006695	OMIM:314390	TAS					P	HPO:skoehler[2015-12-30]
OMIM:314390	VACTERL association, X-linked		HP:0030680	OMIM:314390	IEA					P	HPO:skoehler[2010-06-20]
OMIM:314390	VACTERL association, X-linked		HP:0009623	OMIM:314390	IEA					P	HPO:iea[2009-02-17]
OMIM:314390	VACTERL association, X-linked		HP:0003468	OMIM:314390	TAS					P	HPO:skoehler[2012-10-17]
OMIM:314390	VACTERL association, X-linked		HP:0002575	PMID:20452998;OMIM:314390	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0001561	PMID:20452998	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0005301	PMID:20452998	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0002032	PMID:20452998	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0001161	OMIM:314390	IEA					P	HPO:skoehler[2010-06-20]
OMIM:314390	VACTERL association, X-linked		HP:0031853	OMIM:314390	IEA					P	HPO:skoehler[2018-10-08]
OMIM:314390	VACTERL association, X-linked		HP:0034197	PMID:20452998	PCS		1/1			C	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0000925	OMIM:314390	IEA					P	HPO:iea[2009-02-17]
OMIM:314390	VACTERL association, X-linked		HP:0001419	PMID:20452998	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0003811	PMID:20452998	PCS		1/1			C	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0000960	PMID:20452998	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:314390	VACTERL association, X-linked		HP:0000105	OMIM:314390	TAS					P	HPO:skoehler[2015-12-30]
OMIM:314390	VACTERL association, X-linked		HP:0003974	OMIM:314390	IEA					P	HPO:iea[2009-02-17]
OMIM:314390	VACTERL association, X-linked		HP:0000126	OMIM:314390	IEA					P	HPO:iea[2009-02-17]
OMIM:206780	Anodontia of permanent dentition		HP:0000007	OMIM:206780	IEA					I	HPO:iea[2009-02-17]
OMIM:206780	Anodontia of permanent dentition		HP:0000674	OMIM:206780	TAS					P	HPO:probinson[2009-02-17]
OMIM:251800	Microtia with meatal atresia and conductive deafness		HP:0000154	OMIM:251800	IEA					P	HPO:iea[2009-02-17]
OMIM:251800	Microtia with meatal atresia and conductive deafness		HP:0009892	OMIM:251800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:251800	Microtia with meatal atresia and conductive deafness		HP:0008551	OMIM:251800	IEA					P	HPO:iea[2009-02-17]
OMIM:251800	Microtia with meatal atresia and conductive deafness		HP:0000007	OMIM:251800	IEA					I	HPO:iea[2009-02-17]
OMIM:251800	Microtia with meatal atresia and conductive deafness		HP:0008773	OMIM:251800	IEA					P	HPO:iea[2009-02-17]
OMIM:251800	Microtia with meatal atresia and conductive deafness		HP:0000405	OMIM:251800	IEA					P	HPO:iea[2009-02-17]
OMIM:251800	Microtia with meatal atresia and conductive deafness		HP:0000324	OMIM:251800	IEA					P	HPO:iea[2009-02-17]
OMIM:614173	Joubert syndrome 13		HP:0001320	PMID:21725307	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614173	Joubert syndrome 13		HP:0000007	PMID:26477546	PCS					I	HPO:skoehler[2012-10-17]
OMIM:614173	Joubert syndrome 13		HP:0002419	PMID:21725307	PCS		2/2			P	HPO:probinson[2018-06-12]
OMIM:614173	Joubert syndrome 13		HP:0001302	OMIM:614173	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0003676	OMIM:604360	IEA					C	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000640	OMIM:604360	TAS					P	HPO:probinson[2012-04-06]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002166	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0003596	PMID:17322883	PCS		2/22			C	HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002120	PMID:17322883	PCS		3/16			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001274	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000020	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001251	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002064	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002061	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0003393	OMIM:604360	TAS					P	HPO:probinson[2012-04-25]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0011463	OMIM:604360	TAS					C	HPO:skoehler[2012-11-20]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0007340	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0011462	PMID:17322883	PCS		18/22			C	HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0007067	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002839	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001328	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002518	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001268	OMIM:604360	TAS					P	HPO:probinson[2012-03-12]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001249	PMID:17322883	PCS	HP:0003584	15/22			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002314	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0003202	OMIM:604360	TAS					P	HPO:probinson[2012-04-25]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002015	PMID:17322883	PCS		2/22			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0003621	PMID:17322883	PCS		2/22			C	HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0003487	PMID:17322883	PCS		21/22			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002079	PMID:17322883	PCS		14/16			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001761	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000012	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0002395	PMID:17322883	PCS		21/22			P	HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001260	PMID:17322883	PCS		12/22			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0003380	OMIM:604360	TAS					P	HPO:skoehler[2012-11-20]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0011449	OMIM:604360	TAS					P	HPO:probinson[2012-04-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0011448	OMIM:604360	TAS					P	HPO:probinson[2012-04-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0007350	PMID:17322883	PCS		7/22			P	HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000608	OMIM:604360	TAS	HP:0003581				P	HPO:skoehler[2012-11-20]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0007178	OMIM:604360	TAS					P	HPO:probinson[2012-03-12]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000007	PMID:17322883	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000546	OMIM:604360	TAS	HP:0003581				P	HPO:skoehler[2012-11-20]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000505	OMIM:604360	TAS	HP:0003581				P	HPO:skoehler[2012-11-20]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0030051	OMIM:604360	IEA					P	HPO:iea[2009-02-17]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0000763	OMIM:604360	TAS					P	HPO:probinson[2012-03-12]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001258	OMIM:604360	TAS					P	HPO:probinson[2012-04-06]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0006886	PMID:17322883	PCS		3/17			P	HPO:probinson[2023-01-30]
OMIM:604360	Spastic paraplegia 11, autosomal recessive		HP:0001513	OMIM:604360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158650	Muscular atrophy, malignant neurogenic		HP:0003202	OMIM:158650	TAS					P	HPO:probinson[2012-04-25]
OMIM:158650	Muscular atrophy, malignant neurogenic		HP:0003581	OMIM:158650	TAS					C	HPO:probinson[2012-04-25]
OMIM:158650	Muscular atrophy, malignant neurogenic		HP:0002203	OMIM:158650	TAS					P	HPO:probinson[2012-04-25]
OMIM:158650	Muscular atrophy, malignant neurogenic		HP:0000006	OMIM:158650	TAS					I	HPO:probinson[2012-04-25]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0000252	PMID:29844444	PCS		3/9			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0003212	PMID:29844444	PCS		8/9			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0004322	PMID:29844444	PCS		6/9			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0002750	PMID:29844444	PCS					P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0002719	PMID:29844444	PCS		1/3			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0030353	PMID:29844444	PCS		4/9			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0100646	PMID:29844444	PCS		1/9			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0002608	PMID:29844444	PCS		1/9			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0000964	PMID:29844444	PCS		2/3			P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0008897	PMID:29844444	PCS					P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0000823	PMID:29844444	PCS					P	HPO:probinson[2020-09-10]
OMIM:618985	Growth hormone insensitivity with immune dysregulation 2, autosomal dominant		HP:0000006	PMID:29844444	PCS					I	HPO:probinson[2020-09-10];HPO:probinson[2020-09-10]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000154	PMID:18042262	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2022-04-11]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0002212	PMID:16439621	PCS		3/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0002650	PMID:16439621	PCS		2/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0004322	PMID:18042262	PCS					P	HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0002046	PMID:16439621	PCS		3/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001250	PMID:16439621	PCS		1/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001252	PMID:16439621	PCS		3/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001263	PMID:16439621	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000470	PMID:18042262	PCS					P	HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001629	PMID:18042262	PCS					P	HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000639	PMID:16439621	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2022-04-11]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0032152	PMID:18042262	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001508	PMID:16439621	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001639	PMID:18042262	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000767	PMID:16439621	PCS		3/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000975	PMID:16439621	PCS		3/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000465	PMID:18042262	PCS					P	HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001642	PMID:18042262	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001631	PMID:18042262	PCS					P	HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0004349	PMID:16439621	PCS		1/3			P	HPO:skoehler[2015-08-26];HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0001249	PMID:18042262	PCS					P	HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000006	PMID:18042262	PCS					I	HPO:probinson[2020-07-20]
OMIM:615279	Cardiofaciocutaneous syndrome 3		HP:0000962	PMID:16439621	PCS		3/3			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:614167	Myopia 21, autosomal dominant		HP:0011463	PMID:21695231	PCS		10/10			C	HPO:probinson[2023-03-01]
OMIM:614167	Myopia 21, autosomal dominant		HP:0011003	PMID:21695231	PCS		10/10		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-01]
OMIM:614167	Myopia 21, autosomal dominant		HP:0000006	PMID:21695231	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-01]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0002069	PMID:31664039	PCS					P	HPO:skoehler[2012-11-20];HPO:probinson[2023-06-09]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0003621	PMID:31664039	PCS		2/10			C	HPO:probinson[2023-06-09]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0003596	PMID:31664039	PCS		1/10			C	HPO:probinson[2023-06-09]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0001288	PMID:31664039	PCS	HP:0003581				P	HPO:skoehler[2012-11-20];HPO:probinson[2023-06-09]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0003680	OMIM:613608	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0001340	OMIM:613608	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0001351	OMIM:613608	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0010852	OMIM:613608	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0011462	PMID:31664039	PCS		7/10			C	HPO:probinson[2023-06-09]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0001312	OMIM:613608	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0007359	OMIM:613608	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0000006	PMID:31664039	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0001337	PMID:31664039	PCS		8/10			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-06-09]
OMIM:613608	Epilepsy, familial adult myoclonic, 3		HP:0001336	PMID:31664039	PCS	HP:0003581				P	HPO:skoehler[2012-11-20];HPO:probinson[2023-06-09]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000365	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001250	PMID:10762540	PCS		1/3			P	HP:probinson[2018-07-08]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001252	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001251	PMID:10762540	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002460	PMID:10762540	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001053	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0011382	OMIM:609136	TAS					P	HPO:skoehler[2013-05-31]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000639	PMID:10762540	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001409	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0011461	PMID:10762540	IEA		1/3			C	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002936	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000633	PMID:10762540	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001249	PMID:10762540	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0003623	PMID:10762540	PCS		2/3			C	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001100	PMID:10762540	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001265	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0004336	OMIM:609136	PCS					P	HPO:probinson[2012-04-11]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0006978	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002510	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002595	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001263	PMID:10762540	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0011096	OMIM:609136	PCS					P	HPO:probinson[2012-04-11]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000407	OMIM:609136	PCS		2/2			P	HPO:probinson[2012-04-11]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000966	PMID:10762540	PCS		1/2			P	HP:probinson[2018-07-08]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002227	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000762	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001257	PMID:10762540	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000006	OMIM:609136	IEA					I	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000522	PMID:10762540	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001259	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001336	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002226	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0003693	OMIM:609136	PCS					P	HPO:probinson[2012-04-11]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0004463	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0011284	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0007182	OMIM:609136	PCS					P	HPO:probinson[2012-04-11]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0012332	PMID:10762540	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0011285	PMID:10762540	PCS					P	HPO:probinson[2012-04-11]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0007266	OMIM:609136	PCS					P	HPO:probinson[2012-04-11]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000458	OMIM:609136	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002313	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0007108	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000473	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002059	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001761	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002211	PMID:10762540	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002251	PMID:10762540	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001284	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0002804	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001558	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001319	OMIM:609136	IEA					P	HPO:iea[2009-02-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001510	PMID:10762540	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0001433	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000028	OMIM:609136	TAS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:609136	Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease		HP:0000545	PMID:10762540	PCS		1/3			P	HPO:probinson[2022-03-26]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000286	PMID:33232675	PCS		7/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000486	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0004322	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001250	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001252	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002020	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000085	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000316	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001249	PMID:33232675	PCS		12/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0020206	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0009748	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000358	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002974	PMID:33232675	PCS		1/11			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000176	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002553	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000252	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000494	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0030148	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000574	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0011968	PMID:33232675	PCS		7/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001382	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000293	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0004453	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000490	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001263	PMID:33232675	PCS		12/12			P	HPO:probinson[2021-06-24];HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000294	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0011800	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0010953	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0009890	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000407	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000729	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002308	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000767	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000601	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000527	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000047	PMID:33232675	PCS		1/8			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0009778	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000006	PMID:33232675	PCS					I	HPO:probinson[2021-06-24];HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000369	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0030190	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001655	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000341	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000220	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0010628	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000582	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001792	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000540	PMID:33232675	PCS		3/11			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000463	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0005274	PMID:33232675	PCS		7/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0410170	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0012725	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0010823	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001508	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0012450	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0030043	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000733	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000414	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0009765	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000218	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000411	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002910	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000256	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000395	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002650	PMID:33232675	PCS		2/11			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002376	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002057	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000430	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000270	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0003186	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0045025	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0005280	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0011304	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000708	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002608	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001636	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002209	PMID:33232675	PCS		2/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000426	PMID:33232675	PCS		5/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0012081	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000821	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000307	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000268	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0002007	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000664	PMID:33232675	PCS		4/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000028	PMID:33232675	PCS		1/8			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000545	PMID:33232675	PCS		1/11			P	HPO:probinson[2021-06-24];HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0000347	PMID:33232675	PCS		3/12			P	HPO:probinson[2021-06-24]
OMIM:619325	Coffin-Siris syndrome 12		HP:0001238	PMID:33232675	PCS		1/12			P	HPO:probinson[2021-06-24]
OMIM:600674	Microtia-anotia		HP:0001360	OMIM:600674	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600674	Microtia-anotia		HP:0009892	OMIM:600674	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600674	Microtia-anotia		HP:0008551	OMIM:600674	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600674	Microtia-anotia		HP:0000006	OMIM:600674	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0031956	PMID:27647924	PCS		1/1			P	HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0000750	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0001310	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0002066	PMID:27647924	PCS		1/1			P	HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0001263	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0001251	OMIM:617308	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0003593	PMID:27647924	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0001350	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0002570	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0045014	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0031964	PMID:27647924	PCS		1/1			P	HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0100512	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0000007	PMID:27647924	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:617308	Bile acid synthesis defect, congenital, 6		HP:0000511	PMID:27647924	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-17]
OMIM:602088	Nephronophthisis 2		HP:0004743	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:602088	Nephronophthisis 2		HP:0001562	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:602088	Nephronophthisis 2		HP:0003774	PMID:12872123	PCS	HP:0011463	5/5			P	HPO:iea[2014-01-18];HPO:probinson[2022-05-15]
OMIM:602088	Nephronophthisis 2		HP:0002089	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:602088	Nephronophthisis 2		HP:0001696	OMIM:602088	TAS		1/7			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-05-15]
OMIM:602088	Nephronophthisis 2		HP:0005564	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:602088	Nephronophthisis 2		HP:0002153	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:602088	Nephronophthisis 2		HP:0000090	PMID:12872123	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-05-15]
OMIM:602088	Nephronophthisis 2		HP:0010444	OMIM:602088	TAS					P	HPO:skoehler[2010-06-20]
OMIM:602088	Nephronophthisis 2		HP:0002093	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:602088	Nephronophthisis 2		HP:0004719	OMIM:602088	TAS					P	HPO:probinson[2013-04-12]
OMIM:602088	Nephronophthisis 2		HP:0000822	PMID:12872123	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:602088	Nephronophthisis 2		HP:0000007	PMID:12872123	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:602088	Nephronophthisis 2		HP:0002878	OMIM:602088	TAS					P	HPO:skoehler[2014-06-24]
OMIM:602088	Nephronophthisis 2		HP:0003259	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:602088	Nephronophthisis 2		HP:0000105	OMIM:602088	TAS					P	HPO:probinson[2013-04-12]
OMIM:602088	Nephronophthisis 2		HP:0004734	PMID:12872123	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:602088	Nephronophthisis 2		HP:0005976	OMIM:602088	IEA					P	HPO:iea[2009-02-17]
OMIM:124200	Darier-White disease		HP:0001034	OMIM:124200	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:124200	Darier-White disease		HP:0001250	OMIM:124200	IEA					P	HPO:iea[2009-02-17]
OMIM:124200	Darier-White disease		HP:0200016	OMIM:124200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:124200	Darier-White disease		HP:0010610	OMIM:124200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:124200	Darier-White disease		HP:0011801	OMIM:124200	TAS					P	HPO:probinson[2013-08-11]
OMIM:124200	Darier-White disease		HP:0010612	OMIM:124200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:124200	Darier-White disease		HP:0100792	OMIM:124200	IEA					P	HPO:skoehler[2019-09-07]
OMIM:124200	Darier-White disease		HP:0100753	OMIM:124200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:124200	Darier-White disease		HP:0001807	OMIM:124200	IEA					P	HPO:iea[2009-02-17]
OMIM:124200	Darier-White disease		HP:0008410	OMIM:124200	IEA					P	HPO:iea[2009-02-17]
OMIM:124200	Darier-White disease		HP:0000989	OMIM:124200	TAS					P	HPO:probinson[2009-02-17]
OMIM:124200	Darier-White disease		HP:0007302	OMIM:124200	IEA					P	HPO:iea[2009-02-17]
OMIM:124200	Darier-White disease		HP:6001074	OMIM:124200	TAS					P	HPO:probinson[2024-08-03]
OMIM:124200	Darier-White disease		HP:0000006	OMIM:124200	IEA					I	HPO:iea[2009-02-17]
OMIM:614832	Amelogenesis imperfecta, hypomaturation type, iia4		HP:0000705	PMID:22901946	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:614832	Amelogenesis imperfecta, hypomaturation type, iia4		HP:0006285	PMID:22901946	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:614832	Amelogenesis imperfecta, hypomaturation type, iia4		HP:0006297	PMID:22901946	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:614832	Amelogenesis imperfecta, hypomaturation type, iia4		HP:0000007	PMID:22901946	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-10-01]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0003521	OMIM:313400	TAS					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0007759	OMIM:313400	IEA					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0003621	PMID:14755465	PCS		2/2			C	HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0002650	OMIM:313400	TAS				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0001552	PMID:14755465	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0001376	OMIM:313400	IEA					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0004594	PMID:14755465	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0000470	OMIM:313400	IEA					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0003090	OMIM:313400	TAS					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0100864	PMID:14755465	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0002829	OMIM:313400	IEA					P	HPO:skoehler[2010-06-18]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0000914	OMIM:313400	TAS					P	HPO:skoehler[2014-06-24]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0002808	OMIM:313400	IEA					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0001419	PMID:10431248	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0010582	OMIM:313400	TAS				HP:0012825	P	HPO:iea[2012-05-27]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0002938	OMIM:313400	IEA					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0000926	PMID:14755465	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0002812	OMIM:313400	TAS					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0008897	PMID:14755465	PCS	HP:0003621	2/2			P	HPO:probinson[2023-04-02];HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0003418	PMID:14755465	PCS	HP:0003621	2/2			P	HPO:probinson[2023-04-02];HPO:probinson[2023-04-02]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0008843	OMIM:313400	TAS					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0002866	OMIM:313400	TAS					P	HPO:iea[2009-02-17]
OMIM:313400	Spondyloepiphyseal dysplasia tarda, X-linked		HP:0002655	OMIM:313400	TAS					P	HPO:iea[2009-02-17]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0025066	PMID:26996949	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0004322	PMID:26996949	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0004440	PMID:26996949	PCS					P	HPO:probinson[2017-06-25]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0000482	OMIM:616943	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0001270	OMIM:616943	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0045055	PMID:26996949	PCS		2/2			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0000958	PMID:26996949	PCS		2/2			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0000639	OMIM:616943	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0011001	PMID:26996949	PCS		0/2			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0045048	PMID:26996949	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0002217	PMID:26996949	PCS					P	HPO:probinson[2017-06-25]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0002136	OMIM:616943	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0000252	PMID:26996949	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0008619	PMID:26996949	PCS					P	HPO:probinson[2017-06-25]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0000992	PMID:26996949	PCS		0/2			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0002299	PMID:26996949	PCS		2/2			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0002673	OMIM:616943	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0002750	PMID:26996949	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0001761	OMIM:616943	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0001263	PMID:26996949	PCS		2/2			P	HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0008064	PMID:26996949	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0001518	PMID:26996949	PCS					P	HPO:probinson[2017-06-25]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0000007	PMID:26996949	PCS					I	HPO:probinson[2017-06-25]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0008883	PMID:26996949	PCS					P	HPO:probinson[2017-06-25]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0000565	PMID:26996949	PCS					P	HPO:probinson[2017-06-25]
OMIM:616943	Trichothiodystrophy 6, nonphotosensitive		HP:0002423	PMID:26996949	PCS					P	HPO:probinson[2017-06-25]
OMIM:621123	Achalasia-progeroid syndrome		HP:0007957	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0004322	PMID:35670808	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0001252	PMID:35670808	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0003593	PMID:35670808	PCS		3/5			C	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0031568	PMID:35670808	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0009064	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000958	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0001508	PMID:35670808	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000518	PMID:35670808	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0011463	PMID:35670808	PCS		2/5			C	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000337	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000556	PMID:35670808	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0009803	PMID:35670808	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0001249	PMID:35670808	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000252	PMID:35670808	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0003124	PMID:35670808	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0011968	PMID:35670808	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0002571	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000490	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0011402	PMID:35670808	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0011800	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0034392	PMID:35670808	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0007392	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000407	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000007	PMID:35670808	PCS					I	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0001659	PMID:35670808	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0001653	PMID:35670808	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0003119	PMID:35670808	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621123	Achalasia-progeroid syndrome		HP:0000325	PMID:35670808	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0002069	PMID:10762541	PCS		2/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0003621	PMID:10762541	PCS		2/6			C	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0002078	PMID:10762541	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0002373	PMID:10762541	PCS		2/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0002131	PMID:10762541	PCS		2/11			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0002121	PMID:10762541	PCS		1/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0001260	PMID:10762541	PCS		3/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0010818	PMID:10762541	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0002172	PMID:10762541	PCS		3/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0010532	PMID:10762541	PCS		2/11			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0002392	PMID:10762541	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0011147	PMID:10762541	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0010850	PMID:10762541	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0025709	PMID:10762541	PCS		1/6			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0007193	OMIM:607682	TAS					P	HPO:skoehler[2010-06-18]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0007270	PMID:10762541	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0000639	PMID:10762541	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0011463	PMID:10762541	PCS		2/6			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0007000	PMID:10762541	PCS		1/11			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0025710	PMID:10762541	PCS		1/6			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0001249	PMID:10762541	PCS		0/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0000006	PMID:10762541	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607682	Epilepsy, idiopathic generalized, susceptibility to, 9		HP:0001336	PMID:10762541	PCS		1/11			P	HPO:probinson[2022-09-02]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0003621	PMID:25707578	PCS		1/1			C	HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0001288	PMID:12766226	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0003388	PMID:12766226	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0003473	PMID:12766226	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0003593	PMID:12766226	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0001270	PMID:12766226	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0030208	PMID:25707578;PMID:12766226	PCS		1/2			P	HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0000508	PMID:12766226	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0000007	PMID:12766226	PCS					I	HPO:probinson[2013-08-11];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0003307	PMID:12766226	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0000218	PMID:12766226	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0003768	PMID:25707578;PMID:12766226	PCS		2/2			P	HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0001488	PMID:25707578	PCS		1/1			P	HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0002104	PMID:12766226	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0000544	PMID:25707578	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-08]
OMIM:614198	Myasthenic syndrome, congenital, 16		HP:0003403	PMID:25707578	PCS		1/1			P	HPO:probinson[2023-02-08]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000286	OMIM:615286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000582	OMIM:615286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000486	OMIM:615286	TAS					P	HPO:skoehler[2013-09-10]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0002188	PMID:23620220	PCS		1/15			P	HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0004322	OMIM:615286	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0001250	PMID:23620220	PCS		3/24			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0001274	OMIM:615286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0001252	OMIM:615286	TAS		10/24			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0003593	OMIM:615286	TAS					C	HPO:skoehler[2013-09-10]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0012444	PMID:23620220	PCS		2/15		HP:0012825	P	HPO:skoehler[2019-02-22];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0001508	PMID:23620220	PCS		22/24			P	HPO:skoehler[2013-09-10];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000718	OMIM:615286	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0011220	OMIM:615286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0100702	PMID:23620220	PCS		3/15			P	HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0002119	PMID:23620220	PCS		2/15			P	HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000752	OMIM:615286	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0001249	PMID:23620220	PCS		24/24			P	HPO:skoehler[2013-09-10];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000252	PMID:23620220	PCS		11/24			P	HPO:skoehler[2013-09-10];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0005280	OMIM:615286	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000506	OMIM:615286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000007	PMID:23620220	PCS					I	HPO:skoehler[2013-09-10];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000348	OMIM:615286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000403	OMIM:615286	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000824	OMIM:615286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0000565	PMID:23620220	PCS		22/24			P	HPO:skoehler[2013-09-10];HPO:probinson[2022-11-26]
OMIM:615286	Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies		HP:0001257	PMID:23620220	PCS		7/24			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-11-26]
OMIM:614826	Nystagmus 7, congenital, autosomal dominant		HP:0000006	OMIM:614826	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614826	Nystagmus 7, congenital, autosomal dominant		HP:0007811	OMIM:614826	TAS	HP:0003577				P	HPO:skoehler[2013-08-11]
OMIM:217100	Constricting bands, congenital		HP:0001683	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0000175	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0001762	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0002650	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0002101	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0001161	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0002084	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0002836	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0001547	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0001539	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0000625	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0001159	OMIM:217100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217100	Constricting bands, congenital		HP:0003745	OMIM:217100	IEA					I	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0001543	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0000204	OMIM:217100	IEA					P	HPO:iea[2009-02-17]
OMIM:217100	Constricting bands, congenital		HP:0002006	OMIM:217100	TAS					P	HPO:skoehler[2013-05-31]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0001254	PMID:15505824	PCS	HP:0003623	1/1			P	HPO:probinson[2012-04-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0003577	PMID:15505824	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0002375	PMID:15505824	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0001156	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0011924	PMID:15505824	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0011925	PMID:15505824	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0001274	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0002151	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0011923	PMID:15505824	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0010952	PMID:15505824	PCS	HP:0011461	1/1			P	HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0000969	PMID:15505824	PCS		1/1			P	HPO:probinson[2012-04-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0001518	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0000007	PMID:15505824	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0008872	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0001319	PMID:15505824	PCS	HP:0003623	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0008347	PMID:15505824	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0001643	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0003811	PMID:15505824	PCS		1/1			C	HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0002910	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0005989	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0000369	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:610498	Combined oxidative phosphorylation deficiency 2		HP:0003128	PMID:15505824	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:301010	Myopia 26, X-linked, female-limited		HP:0001417	PMID:27829781	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:301010	Myopia 26, X-linked, female-limited		HP:0011003	PMID:27829781	PCS	HP:0011463	15/15	FEMALE		P	HPO:probinson[2019-06-13]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0001287	OMIM:212050	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0003621	PMID:24131138	PCS					C	HPO:probinson[2022-08-15]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0001871	OMIM:212050	IEA					P	HPO:iea[2009-02-17]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0003212	PMID:24131138	PCS		4/4			P	HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:6000031	PMID:36377664	PCS					P	HPO:probinson[2024-01-06]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0032259	PMID:24131138	PCS					P	HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0012203	PMID:24131138;OMIM:212050	PCS		20/20			P	HP:probinson[2019-06-12];HPO:skoehler[2013-11-28]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0010975	PMID:24131138	PCS		0/17			P	HP:probinson[2019-06-12];HPO:probinson[2022-08-15]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0032515	PMID:24131138	PCS		13/17			P	HP:probinson[2019-06-12];HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0032061	PMID:24131138	PCS		9/10			P	HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0009098	PMID:24131138	PCS		6/17			P	HPO:iea[2009-02-17];HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0040303	PMID:4562433	PCS		10/14			P	HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0025708	PMID:24131138	PCS					C	HPO:probinson[2022-08-15]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0031392	PMID:24131138	PCS		0/17			P	HP:probinson[2019-06-12];HPO:probinson[2022-08-15]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0031393	PMID:24131138	PCS		0/17			P	HP:probinson[2019-06-12];HPO:probinson[2022-08-15]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0011463	PMID:24131138	PCS					C	HPO:probinson[2022-08-15]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0040089	PMID:24131138	PCS		0/17			P	HP:probinson[2019-06-12];HPO:probinson[2022-08-15]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0000007	PMID:24131138	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0002716	PMID:24131138	PCS					P	HP:probinson[2019-06-12]
OMIM:212050	Candidiasis, familial chronic mucocutaneous, autosomal recessive		HP:0002721	OMIM:212050	TAS					P	HPO:skoehler[2013-11-28]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000365	PMID:12687501;PMID:17918734	PCS		23/28			P	HPO:probinson[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000486	PMID:18245432;PMID:12687501	PCS		24/74			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0100490	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000086	PMID:18245432	PCS		1/18			P	HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002020	PMID:17918734	PCS					P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0010722	PMID:17918734	PCS		16/30			P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0012469	PMID:18245432	PCS		15/60			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000518	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000639	PMID:12687501;ISBN-13:978-0721606156	PCS		4/30			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000238	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000878	PMID:18245432	PCS		15/42			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0003745	OMIM:607872	TAS					I	HPO:skoehler[2015-12-30]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002019	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001840	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000358	PMID:18245432;PMID:12687501	PCS		27/90			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000494	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000252	PMID:18245432;PMID:12687501	PCS		57/90			P	HPO:probinson[2021-07-03];HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000892	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000490	PMID:18245432;PMID:12687501;PMID:17918734	PCS		84/90			P	HPO:probinson[2021-07-03];HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0011800	PMID:18245432	PCS		60/60			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0010316	PMID:18245432;PMID:12687501;PMID:17918734	PCS		2/64			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0011097	OMIM:607872	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000407	PMID:18245432;PMID:17918734	PCS		19/42			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03];HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000648	PMID:10507720	PCS					P	HPO:probinson[2012-04-07]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0004209	PMID:12687501;PMID:17918734	PCS		12/30			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000405	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000248	PMID:18245432;PMID:12687501	PCS		57/90			P	HPO:probinson[2021-07-03];HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000369	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002521	PMID:18245432	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000582	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000343	PMID:18245432	PCS		60/60			P	HPO:iea[2012-04-24];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001156	PMID:18245432	PCS		58/70			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002120	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001274	OMIM:607872	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000581	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0008872	PMID:12687501;PMID:17918734	PCS					P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000218	OMIM:607872	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000851	PMID:18245432;PMID:12687501	PCS					P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001302	OMIM:607872	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000457	PMID:12687501	PCS		20/30			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0006956	PMID:18245432;PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002015	PMID:12687501;PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000750	PMID:18245432;PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002650	PMID:18245432	PCS		15/42			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000193	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0011228	PMID:18245432	PCS		60/60			P	HPO:skoehler[2013-10-22];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000902	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0009553	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001319	PMID:18245432	PCS	HP:0003577	57/60			P	HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000505	PMID:18245432;PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002007	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002126	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000588	PMID:18245432	PCS		11/54			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000742	PMID:18245432	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000286	PMID:18245432	PCS		40/70			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002188	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001773	PMID:18245432	PCS		58/70			P	HPO:probinson[2021-07-03];HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002101	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001250	PMID:18031548	PCS	HP:0003593	15/31			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001250	PMID:18245432	PCS		26/60			P	HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001252	PMID:12687501	PCS	HP:0003577	26/30			P	HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000718	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0011220	OMIM:607872	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002616	PMID:12687501	PCS		3/30			P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001647	PMID:12687501;PMID:17918734	PCS		2/30			P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000316	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001643	PMID:18245432;PMID:12687501;PMID:17918734	PCS		9/62			P	HPO:probinson[2021-07-03];HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001249	PMID:18245432;PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001644	PMID:12687501	PCS	HP:0003593	7/30			P	HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001644	PMID:18245432	PCS		2/60			P	HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000176	PMID:12687501	PCS					P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001385	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0004378	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002750	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002079	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002352	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001263	PMID:18245432;PMID:17918734;PMID:18245432	PCS		90/90			P	HPO:probinson[2021-07-03];HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0012817	PMID:18245432	PCS		11/60			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0002591	PMID:20034100	PCS					P	HPO:iea[2011-04-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0012385	PMID:18245432	PCS		48/60			P	HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000202	ISBN-13:978-0721606156	PCS		5/30			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000047	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000204	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001655	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001476	http://www.ncbi.nlm.nih.gov/books/NBK1191/	PCS					P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000540	PMID:12687501	PCS		20/30			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000260	PMID:18245432;PMID:12687501	PCS		52/86			P	HPO:probinson[2021-07-03];HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0010865	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001629	PMID:18245432;PMID:12687501;PMID:17918734	PCS		12/62			P	HPO:probinson[2021-07-03];HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0008551	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000811	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0006897	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000431	PMID:18245432	PCS		60/60			P	HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001761	OMIM:607872	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000391	PMID:17918734	PCS		16/30			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000272	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0005280	PMID:12687501;PMID:17918734	PCS		23/30			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0012760	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001636	PMID:18245432	PCS		2/34			P	HPO:probinson[2021-07-03]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000821	PMID:12687501	PCS		6/30			P	HPO:probinson[2012-04-29]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000307	PMID:18245432;PMID:12687501	PCS		80/90			P	HPO:probinson[2021-07-03];HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0009237	ISBN-13:978-0721606156	PCS		26/30			P	HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000543	PMID:10507720	PCS					P	HPO:probinson[2012-04-07]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000664	PMID:17918734	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001631	PMID:18245432;PMID:12687501;PMID:17918734	PCS		30/44			P	HPO:probinson[2021-07-03];HPO:iea[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001510	ISBN-13:978-0721606156	PCS	HP:0003593				P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000028	PMID:18245432	PCS					P	HPO:iea[2012-04-24]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0000545	PMID:12687501;PMID:17918734	PCS		5/30			P	HPO:probinson[2009-02-17]
OMIM:607872	Chromosome 1p36 deletion syndrome		HP:0001513	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:618952	Combined oxidative phosphorylation deficiency 46		HP:0001410	PMID:26741492	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618952	Combined oxidative phosphorylation deficiency 46		HP:0000007	PMID:26741492	PCS					I	HPO:probinson[2020-08-26];HPO:probinson[2020-08-26]
OMIM:618952	Combined oxidative phosphorylation deficiency 46		HP:0008347	PMID:26741492	PCS		1/1			P	HPO:probinson[2020-08-26];HPO:probinson[2020-08-26]
OMIM:618952	Combined oxidative phosphorylation deficiency 46		HP:0011923	PMID:26741492	IEA		1/1			P	HPO:probinson[2020-08-26]
OMIM:216550	Cohen syndrome		HP:0001135	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0004322	PMID:29149870	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0001250	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0001252	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0010049	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0004283	PMID:29149870	PCS		2/2			P	HPO:skoehler[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0012471	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0002938	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000954	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0002857	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000675	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0001763	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0001249	PMID:29149870	PCS		2/2			P	HPO:skoehler[2010-06-18]
OMIM:216550	Cohen syndrome		HP:0001601	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0003623	PMID:29149870	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0000297	OMIM:216550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:216550	Cohen syndrome		HP:0000494	PMID:29149870	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000252	PMID:29149870	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000574	PMID:29149870	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0008915	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0001382	PMID:29149870	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0002033	PMID:29149870	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0001263	PMID:29149870	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0001182	PMID:29149870	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0007074	PMID:29149870	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000729	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0000327	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000007	PMID:29149870	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0002705	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000648	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000444	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000322	PMID:29149870	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0002943	OMIM:216550	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:216550	Cohen syndrome		HP:0007737	PMID:12446373	PCS		11/13			P	HPO:probinson[2017-12-10]
OMIM:216550	Cohen syndrome		HP:0000189	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0000662	PMID:12446373	PCS		18/22			P	HPO:probinson[2017-12-10]
OMIM:216550	Cohen syndrome		HP:0000580	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0001270	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0010743	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0008872	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0007663	OMIM:216550	TAS					P	HPO:skoehler[2015-07-26]
OMIM:216550	Cohen syndrome		HP:0001786	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0000750	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0001321	OMIM:216550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:216550	Cohen syndrome		HP:0031936	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0001882	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000194	OMIM:216550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:216550	Cohen syndrome		HP:0011504	PMID:12446373	PCS	HP:0011463	5/9			P	HPO:probinson[2017-12-10]
OMIM:216550	Cohen syndrome		HP:0001518	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0011231	PMID:29149870	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0000426	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000824	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0001319	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000505	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0002967	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000823	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0001956	PMID:29149870	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0000347	PMID:29149870	PCS		1/1		HP:0012825	P	HPO:probinson[2012-04-30]
OMIM:216550	Cohen syndrome		HP:0001634	OMIM:216550	IEA					P	HPO:iea[2009-02-17]
OMIM:216550	Cohen syndrome		HP:0000545	PMID:12446373;PMID:29149870	PCS		11/11			P	HPO:probinson[2017-12-10];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:216550	Cohen syndrome		HP:0001875	PMID:29149870	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:261900	Pili torti, early-onset		HP:0002299	OMIM:261900	TAS					P	HPO:skoehler[2013-08-07]
OMIM:261900	Pili torti, early-onset		HP:0006297	OMIM:261900	IEA					P	HPO:iea[2009-02-17]
OMIM:261900	Pili torti, early-onset		HP:0000007	OMIM:261900	IEA					I	HPO:iea[2009-02-17]
OMIM:261900	Pili torti, early-onset		HP:0003329	OMIM:261900	IEA					P	HPO:iea[2009-02-17]
OMIM:261900	Pili torti, early-onset		HP:0002208	OMIM:261900	IEA					P	HPO:iea[2009-02-17]
OMIM:261900	Pili torti, early-onset		HP:0003745	OMIM:261900	TAS					I	HPO:skoehler[2015-12-30]
OMIM:261900	Pili torti, early-onset		HP:0000006	OMIM:261900	TAS					I	HPO:skoehler[2012-10-17]
OMIM:261900	Pili torti, early-onset		HP:0003777	OMIM:261900	IEA					P	HPO:iea[2009-02-17]
OMIM:261900	Pili torti, early-onset		HP:0011359	OMIM:261900	TAS					P	HPO:skoehler[2013-08-07]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001331	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0008749	PMID:2074561	PCS		32/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001177	PMID:2074561	PCS		36/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000142	PMID:2074561	PCS					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0002323	PMID:2074561	PCS		3/56			P	HPO:iea[2018-03-12]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001674	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0002101	PMID:2074561	PCS		35/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000161	OMIM:236680	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236680	Hydrolethalus syndrome 1		HP:0004122	PMID:2074561	PCS		50/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001274	PMID:2074561	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0002282	OMIM:236680	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001629	PMID:2074561	PCS					P	HPO:skoehler[2012-10-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0003826	PMID:2074561	PCS		41/56			C	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001305	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001747	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0002139	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0006379	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0002777	PMID:3321994	PCS		29/38			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000136	OMIM:236680	IEA		50%	FEMALE		P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0002536	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000377	PMID:2074561	PCS		36/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0008216	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0009824	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000175	PMID:2074561	PCS					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001561	PMID:2074561	PCS		51/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000475	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001762	PMID:2074561	PCS		27/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0011803	PMID:2074561	PCS					P	HPO:skoehler[2012-10-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001162	PMID:2074561	PCS		29/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0010066	PMID:2074561	PCS					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000007	OMIM:236680	IEA					I	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0009752	PMID:2074561	PCS		42/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000568	PMID:2074561	PCS		49/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0006882	PMID:2074561	IEA	HP:0003577	47/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001539	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0001511	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0008986	OMIM:236680	IEA					P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000047	OMIM:236680	IEA			MALE		P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000369	PMID:2074561	PCS		36/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000347	PMID:2074561	PCS		56/56			P	HPO:iea[2009-02-17]
OMIM:236680	Hydrolethalus syndrome 1		HP:0000126	PMID:2074561	PCS					P	HPO:iea[2009-02-17]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0030853	PMID:21131972	PCS		3/19			P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0003577	PMID:23255504	PCS		2/11			C	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0001696	PMID:21131972	PCS		10/19			P	HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0003251	PMID:21131972	PCS					P	HPO:probinson[2021-05-11]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0003593	PMID:23255504	PCS		2/11			C	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0012207	PMID:21131972	PCS		4/7	MALE		P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0012208	PMID:23255504	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0011463	PMID:23255504	PCS		2/11			C	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0011462	PMID:23255504	PCS		1/11			C	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0001748	PMID:21131972	PCS		2/19			P	HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0006532	PMID:23255504	PCS		5/11			P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0031417	PMID:23255504	PCS		11/11		HP:0011010	P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0003621	PMID:23255504	PCS		4/11			C	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0002110	PMID:23255504	PCS		9/10			P	HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0012735	PMID:23255504	PCS		9/9		HP:0011010	P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0030828	PMID:23255504	PCS		9/9		HP:0011010	P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0012257	PMID:21131972	PCS					P	HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0011109	PMID:23255504	PCS		11/11			P	HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0012258	PMID:21131972	PCS					P	HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0012265	PMID:21131972	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-05-11]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0012262	OMIM:613807	TAS					P	HPO:probinson[2013-08-07]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0000007	PMID:21131972	PCS					I	HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0002205	PMID:23255504;PMID:21131972	PCS		21/21			P	HPO:probinson[2021-05-09];HPO:probinson[2013-08-07];HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0000388	OMIM:613807	TAS					P	HPO:probinson[2013-08-07]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0002643	PMID:23255504	PCS		9/11			P	HPO:probinson[2021-05-09]
OMIM:613807	Ciliary dyskinesia, primary, 14		HP:0004469	PMID:23255504	PCS		9/9			P	HPO:probinson[2021-05-09]
OMIM:105580	Anal canal carcinomacloacogenic carcinoma, included		HP:0006763	OMIM:105580	IEA					P	HPO:iea[2009-02-17]
OMIM:105580	Anal canal carcinomacloacogenic carcinoma, included		HP:0000006	OMIM:105580	IEA					I	HPO:iea[2009-02-17]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000286	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002144	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000486	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002384	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002263	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000160	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002020	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0003593	PMID:31924697	PCS		1/5			C	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0100890	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0011971	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0033725	PMID:31924697	PCS		2/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0012471	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0012450	PMID:31924697	PCS		2/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000316	PMID:31924697	PCS		2/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0006695	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002414	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000378	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000455	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001643	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001249	PMID:31924697	PCS		5/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000358	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0003623	PMID:31924697	PCS		4/5			C	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000473	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000494	PMID:31924697	PCS		2/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000750	PMID:31924697	PCS		5/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001344	PMID:31924697	PCS		3/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002650	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000431	PMID:31924697	PCS		2/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0011968	PMID:31924697	PCS		3/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000391	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000193	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001263	PMID:31924697	PCS		5/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001680	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002194	PMID:31924697	PCS		5/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001182	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0012799	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000729	PMID:31924697	PCS		2/4			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001338	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000348	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002007	PMID:31924697	PCS		2/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000268	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0001357	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0002349	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000006	PMID:31924697	PCS					I	HPO:probinson[2021-10-15];HPO:probinson[2021-10-15]
OMIM:619480	Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum		HP:0000369	PMID:31924697	PCS		1/5			P	HPO:probinson[2021-10-15]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0002421	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0008936	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0002169	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0002376	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0001250	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0003121	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0001263	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0003593	PMID:35262690	PCS		1/1			C	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0012301	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0033725	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0100275	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0011471	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0034353	PMID:35262690	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620201	Congenital disorder of glycosylation, type IIz		HP:0000007	PMID:35262690	PCS					I	HPO:probinson[2023-06-11]
OMIM:300454	Intellectual developmental disorder, X-linked 77		HP:0002373	OMIM:300454	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300454	Intellectual developmental disorder, X-linked 77		HP:0001419	OMIM:300454	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300454	Intellectual developmental disorder, X-linked 77		HP:0000752	OMIM:300454	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300454	Intellectual developmental disorder, X-linked 77		HP:0001249	OMIM:300454	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000341	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000582	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0006824	OMIM:611962	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000023	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0004322	OMIM:611962	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000581	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0012745	OMIM:611962	TAS					P	HPO:skoehler[2014-03-24]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000239	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0001647	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0002858	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000219	OMIM:611962	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0001643	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0002656	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0001840	OMIM:611962	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000472	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0002650	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0002750	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0003088	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000270	OMIM:611962	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000272	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0004691	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0011800	OMIM:611962	TAS					P	HPO:skoehler[2013-11-28]
OMIM:611962	Hunter-Macdonald syndrome		HP:0012385	OMIM:611962	TAS				HP:0003676	P	HPO:skoehler[2013-10-22]
OMIM:611962	Hunter-Macdonald syndrome		HP:0010584	OMIM:611962	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000407	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0009473	OMIM:611962	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000508	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000822	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0001537	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000348	OMIM:611962	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000405	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000768	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0001659	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0002967	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0004209	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000047	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000322	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0001653	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000006	OMIM:611962	IEA					I	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000248	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0000545	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611962	Hunter-Macdonald syndrome		HP:0001634	OMIM:611962	IEA					P	HPO:skoehler[2010-06-19]
OMIM:121350	Coracoclavicular joint, anomalous		HP:0001367	OMIM:121350	IEA					P	HPO:iea[2009-02-17]
OMIM:121350	Coracoclavicular joint, anomalous		HP:0000006	OMIM:121350	IEA					I	HPO:iea[2009-02-17]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000343	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000463	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0001250	PMID:30293988;PMID:29276006	PCS		3/6			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0001274	PMID:30293988	PCS					P	HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0003196	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0011320	PMID:30293988	PCS		1/5			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000316	PMID:30293988;PMID:29276006	PCS		11/11			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000238	PMID:30293988	PCS		1/5			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0002119	PMID:30293988	PCS					P	HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0030084	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0003049	PMID:30293988	PCS					P	HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0002650	PMID:30293988	PCS		2/5			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000431	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0002079	PMID:30293988;PMID:29276006	PCS		11/11			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0011968	PMID:30293988	PCS		4/5			P	HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0012815	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0001263	PMID:30293988;PMID:29276006	PCS		6/6			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0011800	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000527	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0001357	PMID:30293988	PCS					P	HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000289	PMID:30293988	PCS					P	HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000520	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000006	PMID:30293988	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000028	PMID:30293988	PCS		1/4	MALE		P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000248	PMID:30293988	PCS					P	HPO:probinson[2020-07-23]
OMIM:618577	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies		HP:0000347	PMID:29276006	PCS		1/1			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:617644	Spermatogenic failure 21		HP:0011462	PMID:28199965	PCS		1/1			C	HPO:probinson[2023-06-10]
OMIM:617644	Spermatogenic failure 21		HP:0003251	PMID:28199965	PCS		1/1			P	HPO:probinson[2023-06-10]
OMIM:617644	Spermatogenic failure 21		HP:0012207	PMID:28199965	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-10]
OMIM:617644	Spermatogenic failure 21		HP:0000007	PMID:28199965	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-10]
OMIM:617644	Spermatogenic failure 21		HP:0012869	PMID:28199965	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-10]
OMIM:139090	Gray platelet syndrome		HP:0000132	OMIM:139090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:139090	Gray platelet syndrome		HP:0001892	OMIM:139090	IEA					P	HPO:iea[2009-02-17]
OMIM:139090	Gray platelet syndrome		HP:0003676	OMIM:139090	TAS					C	HPO:skoehler[2012-10-17]
OMIM:139090	Gray platelet syndrome		HP:0003010	OMIM:139090	IEA					P	HPO:iea[2009-02-17]
OMIM:139090	Gray platelet syndrome		HP:0012528	PMID:21765412	PCS					P	HPO:probinson[2020-07-17]
OMIM:139090	Gray platelet syndrome		HP:0012147	OMIM:139090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139090	Gray platelet syndrome		HP:0011872	OMIM:139090	TAS					P	HPO:probinson[2012-05-30]
OMIM:139090	Gray platelet syndrome		HP:0011974	OMIM:139090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139090	Gray platelet syndrome		HP:0008330	OMIM:139090	IEA					P	HPO:iea[2009-02-17]
OMIM:139090	Gray platelet syndrome		HP:0008320	OMIM:139090	TAS					P	HPO:probinson[2012-05-30]
OMIM:139090	Gray platelet syndrome		HP:0000007	PMID:21765412	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-07-17]
OMIM:139090	Gray platelet syndrome		HP:0000978	OMIM:139090	TAS					P	HPO:skoehler[2009-02-17]
OMIM:139090	Gray platelet syndrome		HP:0001873	OMIM:139090	IEA					P	HPO:iea[2009-02-17]
OMIM:139090	Gray platelet syndrome		HP:0000421	OMIM:139090	TAS					P	HPO:probinson[2009-02-17]
OMIM:139090	Gray platelet syndrome		HP:0001744	OMIM:139090	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000561	OMIM:106260	IEA					P	HPO:skoehler[2012-10-12]
OMIM:106260	Hay-Wells syndrome		HP:0003577	PMID:15200513	PCS		1/1			C	HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0001795	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0001592	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0410030	PMID:14684701	PCS		1/3			P	HPO:probinson[2024-03-06]
OMIM:106260	Hay-Wells syndrome		HP:0001629	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000953	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000653	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0001643	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0002558	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000498	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0001249	PMID:14684701	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-06]
OMIM:106260	Hay-Wells syndrome		HP:0000413	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000698	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000054	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000175	PMID:14684701;PMID:15200513	PCS		2/4			P	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11];HPO:probinson[2024-03-06];HPO:probinson[2024-03-06]
OMIM:106260	Hay-Wells syndrome		HP:0000431	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0002232	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000970	PMID:14684701	PCS		3/3			P	HPO:probinson[2024-03-06]
OMIM:106260	Hay-Wells syndrome		HP:0002231	PMID:14684701	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:106260	Hay-Wells syndrome		HP:0004691	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0011470	PMID:19353643	PCS		7/12			P	HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0000968	PMID:15200513	PCS		1/1			P	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0000509	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000707	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0031088	OMIM:106260	TAS					P	HPO:skoehler[2017-07-13]
OMIM:106260	Hay-Wells syndrome		HP:0000327	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000668	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0009755	PMID:14684701;PMID:15200513;PMID:19353643	PCS		14/16			P	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11];HPO:probinson[2024-03-06];HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0000405	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0008404	PMID:14684701	PCS		3/3			P	HPO:skoehler[2013-05-03];HPO:probinson[2024-03-06]
OMIM:106260	Hay-Wells syndrome		HP:0000982	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000300	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000564	PMID:19353643	PCS		10/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0000047	PMID:19353643	PCS		6/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0000006	PMID:10535733	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0000204	PMID:19353643	PCS		10/12			P	HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0000687	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0004502	PMID:15200513	PCS		1/1			P	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:106260	Hay-Wells syndrome		HP:0001798	OMIM:106260	IEA					P	HPO:iea[2009-02-17]
OMIM:106260	Hay-Wells syndrome		HP:0000522	PMID:14684701	PCS		3/3			P	HPO:probinson[2024-03-06]
OMIM:106260	Hay-Wells syndrome		HP:0003777	PMID:14684701	PCS		3/3			P	HPO:probinson[2024-03-06]
OMIM:611553	Noonan syndrome 5		HP:0000286	PMID:17603483	PCS		13/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001792	PMID:17603483	PCS		1/23			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0004322	PMID:17603482;PMID:17603483	PCS		30/33			P	HPO:probinson[2013-04-06];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0011675	OMIM:611553	TAS					P	HPO:skoehler[2018-10-08]
OMIM:611553	Noonan syndrome 5		HP:0045075	PMID:17603483	PCS		2/23			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000958	PMID:17603483	PCS		8/23			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000957	PMID:17603483	PCS		4/22			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0011220	PMID:17603483	PCS		18/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0012471	PMID:17603483	PCS		8/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000316	PMID:17603483	PCS		22/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000256	PMID:17603483	PCS		17/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001642	PMID:17603483	PCS		5/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001249	PMID:17603483	PCS		8/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001601	PMID:17603483	PCS		4/18			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0002212	PMID:17603483	PCS		6/23			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000154	PMID:17603483	PCS		5/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000494	PMID:17603483	PCS		21/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0003764	PMID:17603483	PCS		8/23			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001561	PMID:17603483	PCS	HP:0011461	6/19			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0002213	PMID:17603483	PCS		3/23			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001520	PMID:17603483	PCS		6/22			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001003	PMID:17603483	PCS		4/23			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000391	PMID:17603483	PCS		20/23			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001263	PMID:17603482	PCS					P	HPO:probinson[2013-04-06]
OMIM:611553	Noonan syndrome 5		HP:0000470	PMID:17603482;PMID:17603483	PCS		15/32			P	HPO:probinson[2013-01-09];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0005280	PMID:17603483	PCS		14/23			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0032152	PMID:17603483	PCS		2/23			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001639	PMID:17603482;PMID:17603483	PCS		24/34			P	HPO:probinson[2013-04-06];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000508	PMID:17603483	PCS		20/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001999	PMID:17603482	PCS					P	HPO:probinson[2013-04-06]
OMIM:611553	Noonan syndrome 5		HP:0000766	PMID:17603482	PCS					P	HPO:probinson[2013-04-06]
OMIM:611553	Noonan syndrome 5		HP:0002967	PMID:17603483	PCS		8/23			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000268	PMID:17603483	PCS		12/22			P	HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0001631	PMID:17603482;PMID:17603483	PCS		11/34			P	HPO:probinson[2013-04-06];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000465	PMID:17603482;PMID:17603483	PCS		12/31			P	HPO:probinson[2013-04-06];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000006	PMID:17603482	PCS					I	HPO:probinson[2013-04-06]
OMIM:611553	Noonan syndrome 5		HP:0000028	PMID:17603483	PCS		6/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000369	PMID:17603483	PCS		20/23			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22]
OMIM:611553	Noonan syndrome 5		HP:0000303	PMID:17603483	PCS		13/21			P	HPO:probinson[2021-05-22]
OMIM:615735	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse		HP:0025092	OMIM:615735	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615735	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse		HP:0007556	PMID:19609311	PCS				HP:0030650	P	HPO:probinson[2022-09-11]
OMIM:615735	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse		HP:0000982	OMIM:615735	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615735	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse		HP:0002745	PMID:19609311	PCS		1/17			P	HPO:probinson[2022-09-11]
OMIM:615735	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse		HP:0000006	PMID:19609311	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2022-09-11]
OMIM:142350	Hernia, double inguinal		HP:0000023	OMIM:142350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:142350	Hernia, double inguinal		HP:0000006	OMIM:142350	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:615721	Renal hypodysplasia/aplasia 2		HP:0010958	PMID:22698282	PCS		4/4			P	HPO:probinson[2023-01-30]
OMIM:615721	Renal hypodysplasia/aplasia 2		HP:0002089	PMID:22698282	PCS		1/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-30]
OMIM:615721	Renal hypodysplasia/aplasia 2		HP:0030674	PMID:22698282	PCS		4/4			C	HPO:probinson[2023-01-30]
OMIM:615721	Renal hypodysplasia/aplasia 2		HP:0001582	PMID:22698282	PCS		1/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-30]
OMIM:615721	Renal hypodysplasia/aplasia 2		HP:0000007	PMID:22698282	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-30]
OMIM:615721	Renal hypodysplasia/aplasia 2		HP:0002009	PMID:22698282	PCS		1/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-01-30]
OMIM:615721	Renal hypodysplasia/aplasia 2		HP:0025700	PMID:22698282	PCS		4/4			P	HPO:probinson[2023-01-30]
OMIM:194070	Wilms tumor 1		HP:0001442	OMIM:194070	IEA					I	HPO:iea[2009-02-17]
OMIM:194070	Wilms tumor 1		HP:0002667	OMIM:194070	IEA					P	HPO:iea[2009-02-17]
OMIM:194070	Wilms tumor 1		HP:0000006	OMIM:194070	IEA					I	HPO:iea[2009-02-17]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000286	OMIM:618205	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000483	PMID:30397230	PCS		2/35			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000486	PMID:30397230	PCS		10/33			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000540	PMID:30397230	PCS		11/29			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000023	PMID:30397230	PCS		3/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0025268	PMID:30397230	PCS		2/35			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001252	PMID:30397230	PCS		21/28			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0003593	PMID:30397230	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0032794	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0033725	PMID:30397230	PCS		2/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0012766	PMID:30397230	PCS		10/30			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0012469	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0100704	PMID:30397230	PCS		3/33			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0011220	OMIM:618205	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0011682	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0006297	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000316	PMID:30397230	PCS		24/31			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000679	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000733	PMID:30397230	PCS		2/35			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0002317	PMID:30397230	PCS		5/35			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0002119	OMIM:618205	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000218	PMID:30397230	PCS		9/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000256	PMID:30397230	PCS		19/31			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001642	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001249	PMID:30397230	PCS		35/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001760	OMIM:618205	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0002136	PMID:30397230	PCS		4/35			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000750	PMID:29463886;PMID:30397230	PCS		34/34			P	HPO:probinson[2023-02-10];HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0002650	PMID:30397230	PCS		2/35			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000431	OMIM:618205	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0031936	OMIM:618205	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0011968	PMID:30397230	PCS	HP:0003623	10/32			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001382	PMID:30397230	PCS		12/30			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001260	PMID:30397230	PCS		1/35			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001263	PMID:30397230	PCS		35/35			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0011800	OMIM:618205	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000729	PMID:30397230	PCS		9/31			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0011098	PMID:29463886	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000448	OMIM:618205	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001537	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0002007	PMID:30397230	PCS		28/33			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0007018	PMID:30397230	PCS		3/24			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0001631	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000006	PMID:29463886	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000369	OMIM:618205	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618205	Snijders Blok-Campeau syndrome		HP:0000687	PMID:30397230	PCS		1/35			P	HPO:probinson[2023-02-10]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0020152	PMID:23404334	PCS		3/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003473	PMID:23404334	PCS		5/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0001252	PMID:23404334	PCS		3/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003691	PMID:23404334	PCS		1/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003593	PMID:23404334	PCS		2/5			C	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0001270	PMID:23404334	PCS		5/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003391	PMID:23404334	PCS		1/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0030319	PMID:23404334	PCS		4/5			P	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0100301	PMID:23404334	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0011463	PMID:23404334	PCS		3/5			C	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003307	PMID:23404334	PCS		1/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0002515	PMID:23404334	PCS		1/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0000218	PMID:23404334	PCS		3/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003803	PMID:23404334	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0001763	PMID:23404334	PCS		3/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003325	PMID:23404334	PCS		5/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003403	PMID:23404334	PCS		3/3			P	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003687	PMID:23404334	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003200	OMIM:616228	TAS		HP:0040283			P	HPO:skoehler[2015-03-22]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0002650	OMIM:616228	TAS		HP:0040283			P	HPO:skoehler[2015-03-22]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0008180	PMID:23404334	PCS		2/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0006380	PMID:23404334	PCS		3/5			P	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0000508	PMID:23404334	PCS		0/5			P	HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0000007	PMID:23404334	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003677	PMID:23404334	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:616228	Myasthenic syndrome, congenital, 14		HP:0003557	PMID:23404334	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0003236	PMID:15792865	PCS		5/5			P	HPO:iea[2009-02-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0000252	OMIM:609308	IEA					P	HPO:iea[2009-02-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0001288	OMIM:609308	TAS					P	HPO:probinson[2012-05-26]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0003388	OMIM:609308	IEA					P	HPO:iea[2009-02-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0031936	PMID:15792865	PCS		5/5			P	HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0001387	PMID:15792865	PCS		2/5			P	HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0001371	OMIM:609308	IEA					P	HPO:iea[2009-02-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0003551	PMID:15792865	PCS		5/5			P	HPO:probinson[2012-05-26];HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0030046	PMID:15792865	PCS		5/5			P	HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0003560	OMIM:609308	IEA					P	HPO:iea[2009-02-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0001270	OMIM:609308	TAS					P	HPO:probinson[2009-02-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0011463	PMID:15792865	PCS		5/5			C	HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0008981	PMID:15792865	PCS		4/5			P	HPO:probinson[2023-05-09];HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0002938	OMIM:609308	IEA					P	HPO:iea[2009-02-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0000007	PMID:15792865	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0001638	OMIM:609308	TAS		HP:0040283			P	HPO:skoehler[2013-02-25]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0003306	OMIM:609308	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0001249	PMID:15792865	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0003325	PMID:15792865	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-09]
OMIM:609308	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1		HP:0003677	PMID:15792865	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-05-09]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0006429	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001531	PMID:16537452	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001773	OMIM:611209	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0004322	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0005575	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000160	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000083	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001252	PMID:16537452	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000162	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0012301	PMID:16537452;PMID:19008299	PCS		2/2			P	HPO:probinson[2023-02-20];HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0011342	OMIM:611209	IEA					P	HPO:skoehler[2019-09-07]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000319	PMID:19008299	PCS		1/2			P	HPO:probinson[2013-04-01];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0009465	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000316	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000954	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0020045	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0008897	PMID:19008299	PCS		1/2			P	HPO:probinson[2013-04-01];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000358	PMID:19008299	PCS		2/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0002751	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000253	OMIM:611209	TAS					P	HPO:probinson[2013-04-01]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000175	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000494	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000252	PMID:19008299	PCS		2/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001263	PMID:19008299;OMIM:611209	PCS		3/3			P	HPO:probinson[2013-04-01];HPO:probinson[2021-04-25];HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0011800	OMIM:611209	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0012385	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000007	PMID:19008299	PCS					I	HPO:probinson[2013-04-01];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000405	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0003316	PMID:19008299	PCS		1/2			P	HPO:probinson[2013-04-01]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000047	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000201	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000520	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0002943	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000369	PMID:19008299	PCS		2/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000402	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000126	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0003577	PMID:16537452	IEA		1/1			C	HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000582	PMID:16537452	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000343	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0008905	PMID:16537452;PMID:19008299	PCS		2/3			P	HPO:probinson[2013-04-01];HPO:probinson[2021-04-25];HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000463	OMIM:611209	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001272	PMID:16537452	PCS	HP:0011463	1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0003177	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0012444	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0003090	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0002719	OMIM:611209	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001903	OMIM:611209	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000938	PMID:19008299	PCS		1/2			P	HPO:probinson[2013-04-01]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0008551	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0008872	PMID:16537452	PCS		1/1			P	HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001902	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000219	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000218	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0030282	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0006610	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001320	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0003026	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0003422	PMID:19008299	PCS		1/2			P	HPO:probinson[2013-04-01];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0002059	PMID:16537452	PCS	HP:0011463	1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0006956	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000274	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000750	OMIM:611209	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001762	PMID:19008299	PCS		1/2			P	HPO:probinson[2013-04-01];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000431	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0031936	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000470	PMID:19008299	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0003182	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000902	PMID:19008299	PCS		2/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0009797	PMID:19008299	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001712	PMID:16537452	PCS	HP:0003593	1/1			P	HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001511	OMIM:611209	IEA					P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0200055	PMID:16537452	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-04-25]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0001873	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-20]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000028	PMID:19008299	PCS		1/2			P	HPO:skoehler[2019-02-22]
OMIM:611209	Congenital disorder of glycosylation, type IIg		HP:0000347	PMID:19008299	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-20]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0010849	PMID:15937479	PCS		3/13			P	HPO:probinson[2013-02-25];HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0003621	PMID:15937479	PCS		5/13			C	HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0001250	PMID:26195193	PCS		0/2			P	HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0002121	PMID:15937479	PCS		6/13			P	HPO:probinson[2013-02-25];HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0001263	PMID:26195193	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0001252	PMID:26195193	PCS		1/2			P	HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0003593	PMID:15937479;PMID:26195193	PCS		2/15			C	HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0025190	PMID:15937479	PCS		2/13			P	HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0011463	PMID:15937479	PCS		7/13			C	HPO:probinson[2023-03-08];HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0007166	PMID:15937479;PMID:26195193	PCS		14/15			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-08];HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0000006	PMID:15937479	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0001348	PMID:26195193	PCS		2/2			P	HPO:probinson[2023-03-08]
OMIM:609446	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy		HP:0003623	PMID:26195193	PCS		1/2			C	HPO:probinson[2023-03-08]
OMIM:616566	Spondylocostal dysostosis 6, autosomal recessive		HP:0002650	PMID:25343988	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:616566	Spondylocostal dysostosis 6, autosomal recessive		HP:0002937	PMID:25343988	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:616566	Spondylocostal dysostosis 6, autosomal recessive		HP:0000007	PMID:25343988	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-06]
OMIM:616566	Spondylocostal dysostosis 6, autosomal recessive		HP:0002947	PMID:25343988	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-06]
OMIM:616566	Spondylocostal dysostosis 6, autosomal recessive		HP:0003316	PMID:25343988	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:616566	Spondylocostal dysostosis 6, autosomal recessive		HP:0003416	PMID:25343988	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-06]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000396	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000143	OMIM:608980	TAS					P	HPO:probinson[2013-03-30]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000200	PMID:19732862;PMID:32926405	PCS		11/12			P	HP:probinson[2021-10-22];HPO:probinson[2020-07-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000574	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000122	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0011803	PMID:19732862;PMID:32926405	PCS		11/11			P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-22];HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0010316	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000826	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000007	PMID:19732862	PCS					I	HPO:probinson[2013-03-30]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000414	PMID:19732862	PCS					P	HPO:probinson[2013-03-30];HPO:probinson[2020-07-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0001566	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000322	OMIM:608980	TAS					P	HPO:probinson[2013-03-30]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000248	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000369	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000358	PMID:32926405	PCS		1/2			P	HP:probinson[2021-10-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0001545	PMID:19732862	PCS					P	HPO:probinson[2013-03-30];HPO:probinson[2020-07-22]
OMIM:608980	Bifid nose with or without anorectal and renal anomalies		HP:0000104	PMID:19732862	PCS		6/9			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0001663	PMID:12404107	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0002321	PMID:12404107	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0001670	PMID:12404107	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0005144	PMID:12404107	PCS					P	HPO:probinson[2013-03-25];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0003581	PMID:12404107	PCS		7/7			C	HPO:probinson[2022-07-10]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0002094	PMID:12404107	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0010872	PMID:12404107;PMID:9535554	PCS		14/22			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-21];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0011713	PMID:12404107	PCS		1/7			P	HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0031656	PMID:9535554	PCS		8/16			P	HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0001639	PMID:8673105	PCS		4/4			P	HPO:probinson[2013-01-09];HPO:probinson[2021-10-14]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0001712	PMID:9535554	PCS		13/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0100749	PMID:12404107	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0001962	PMID:12404107	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0000006	PMID:8673105	PCS					I	HPO:probinson[2013-03-25];HPO:probinson[2021-10-14]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0001645	PMID:12404107	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0004756	PMID:12404107	PCS					P	HPO:probinson[2013-03-25];HPO:probinson[2021-10-21]
OMIM:608758	Cardiomyopathy, familial hypertrophic, 10		HP:0004755	PMID:12404107	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-21]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0002023	PMID:24253444	PCS		1/3			P	HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0000122	PMID:24253444	PCS		1/3			P	HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0034199	PMID:24253444	PCS		1/3			C	HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0034198	PMID:24253444	PCS		1/3			C	HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0000007	PMID:24253444	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0003811	PMID:24253444	PCS		3/3			C	HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0010305	PMID:24253444	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0012621	PMID:24253444	PCS		1/3			P	HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0003468	PMID:24253444	PCS		3/3			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-06-10]
OMIM:615709	Sacral agenesis with vertebral anomalies		HP:0008428	PMID:24253444	PCS		1/3			P	HPO:probinson[2023-06-10]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0002069	PMID:21922598	PCS		1/4			P	HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0003621	PMID:21922598	PCS		2/4			C	HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0002384	PMID:21922598	PCS		1/4			P	HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0011463	PMID:21922598	PCS		2/4			C	HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0000007	PMID:21922598	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0010850	PMID:21922598	PCS		1/4			P	HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0002349	PMID:21922598	PCS		3/4			P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0000006	OMIM:614417	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0001249	PMID:21922598	PCS		1/4			P	HPO:probinson[2021-06-26]
OMIM:614417	Epilepsy, familial temporal lobe, 5		HP:0020216	PMID:21922598	PCS		1/4			P	HPO:probinson[2021-06-26]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001892	OMIM:266510	IEA					P	HPO:skoehler[2010-06-20]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0003577	OMIM:266510	IEA					C	HPO:skoehler[2010-06-19]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:6000396	PMID:12701824	PCS					P	HPO:probinson[2024-02-27]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:6000393	OMIM:266510	TAS					P	HPO:probinson[2024-02-27]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001271	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001252	PMID:15184617	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0002240	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001251	PMID:15184617	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0030473	PMID:15184617	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0003593	PMID:15184617	PCS		1/1			C	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001290	OMIM:266510	TAS					P	HPO:skoehler[2017-07-13]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0012368	OMIM:266510	TAS					P	HPO:skoehler[2013-10-22]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000939	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001508	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000639	PMID:15184617	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0010571	PMID:15184617	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000954	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0020045	PMID:15184617	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000510	PMID:15184617	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000457	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001249	PMID:15184617	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000556	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001265	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0003146	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001260	PMID:15184617	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001263	PMID:15184617	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000272	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0002570	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001284	PMID:15184617	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000407	PMID:15184617	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0008167	OMIM:266510	IEA					P	HPO:iea[2009-02-17]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0001999	OMIM:266510	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:266510	Peroxisome biogenesis disorder 3B		HP:0000007	PMID:14571262	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:158320	Muir-Torre syndrome		HP:0006758	OMIM:158320	IEA					P	HPO:iea[2009-02-17]
OMIM:158320	Muir-Torre syndrome		HP:0003002	OMIM:158320	IEA					P	HPO:iea[2009-02-17]
OMIM:158320	Muir-Torre syndrome		HP:0003596	PMID:14994245	PCS		3/3			C	HPO:probinson[2022-06-18]
OMIM:158320	Muir-Torre syndrome		HP:0003003	PMID:14994245	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-18]
OMIM:158320	Muir-Torre syndrome		HP:0030410	PMID:14994245	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-18]
OMIM:158320	Muir-Torre syndrome		HP:0002253	OMIM:158320	IEA					P	HPO:iea[2009-02-17]
OMIM:158320	Muir-Torre syndrome		HP:0002671	OMIM:158320	IEA					P	HPO:iea[2009-02-17]
OMIM:158320	Muir-Torre syndrome		HP:0006719	OMIM:158320	IEA					P	HPO:iea[2009-02-17]
OMIM:158320	Muir-Torre syndrome		HP:0012118	OMIM:158320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158320	Muir-Torre syndrome		HP:0100615	PMID:14994245	PCS		1/1			P	HPO:probinson[2022-06-18]
OMIM:158320	Muir-Torre syndrome		HP:0006771	OMIM:158320	IEA					P	HPO:iea[2009-02-17]
OMIM:158320	Muir-Torre syndrome		HP:0009720	OMIM:158320	TAS					P	HPO:skoehler[2014-04-04]
OMIM:158320	Muir-Torre syndrome		HP:0000006	PMID:14994245	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-18]
OMIM:158320	Muir-Torre syndrome		HP:0006778	OMIM:158320	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000980	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001252	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003691	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003593	PMID:17056637	PCS		1/2			C	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000580	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001290	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003391	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0012132	OMIM:600462	TAS					P	HPO:skoehler[2013-06-13]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001508	OMIM:600462	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0011463	PMID:17056637	PCS		1/2			C	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000316	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003307	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001924	PMID:17056637	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0009743	OMIM:600462	TAS		HP:0040284			P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000218	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001324	PMID:17056637	PCS		2/2			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003688	PMID:17056637	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000457	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001249	PMID:17056637	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003546	PMID:17056637	PCS		0/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003128	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003323	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000252	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0020081	OMIM:600462	IEA					P	HPO:skoehler[2019-04-18]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003200	PMID:17056637	PCS		1/1			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001382	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0002151	PMID:17056637	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0040075	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0011923	PMID:17056637	PCS		2/2			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0003281	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0002091	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0009055	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000007	PMID:15108122	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0008347	PMID:17056637	PCS		2/2			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001935	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000823	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001510	PMID:17056637	PCS		1/2			P	HPO:probinson[2023-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0001931	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:600462	Myopathy, lactic acidosis, and sideroblastic anemia 1		HP:0000347	OMIM:600462	IEA					P	HPO:iea[2009-02-17]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0004325	PMID:25261934	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0004322	PMID:25261934	PCS		1/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0008070	PMID:25261934	PCS		0/3			P	HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000939	PMID:25261934	PCS		0/3			P	HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000518	PMID:25261934	PCS		1/3			P	HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000954	PMID:25261934	PCS		3/3			P	HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000414	OMIM:616200	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0009125	PMID:25261934	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0030084	OMIM:616200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0007787	OMIM:616200	TAS				HP:0012832	P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0002216	PMID:25261934	PCS		1/3			P	HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0200021	OMIM:616200	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0001763	OMIM:616200	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000135	PMID:25261934	PCS		0/3			P	HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0001402	PMID:25261934	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0003202	PMID:25261934	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0002750	PMID:25261934	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000767	OMIM:616200	TAS				HP:0012825	P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000426	OMIM:616200	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000007	PMID:25261934	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0002007	OMIM:616200	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0002987	OMIM:616200	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0005659	OMIM:616200	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000347	PMID:25261934	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:616200	Ruijs-Aalfs syndrome		HP:0000325	PMID:25261934	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-04]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0100315	PMID:28817800	PCS		5/5			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0003596	PMID:28817800	PCS		3/9			C	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0002354	PMID:28817800	PCS		1/9			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0002145	PMID:28817800	PCS		5/9			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0001283	PMID:28817800	PCS		3/9			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0003584	PMID:28817800	PCS		5/9			C	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0011462	PMID:28817800	PCS		1/9			C	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0007354	PMID:28817800	PCS		8/9			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0002381	PMID:28817800	PCS		3/9			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0003690	PMID:28817800	PCS		2/9			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0000751	PMID:28817800	PCS		1/9			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619133	Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia		HP:0000006	PMID:28817800	PCS					I	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001332	PMID:27623250	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001250	PMID:30642748	PCS		0/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0012706	PMID:27623250	PCS		1/1			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0002063	PMID:18614015	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0012707	PMID:30642748	PCS		1/1			P	HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001252	PMID:30642748	PCS					P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0003593	PMID:18614015	PCS		2/2			C	HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001251	PMID:18614015;PMID:30642748	PCS		3/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0012128	PMID:30642748	PCS		3/3			P	HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0011463	PMID:27623250;PMID:30642748	PCS		4/4			C	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001324	PMID:18614015	PCS		2/2			P	HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0007325	PMID:30642748	PCS		3/3			P	HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001763	PMID:27623250	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0003128	PMID:18614015	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0003202	OMIM:618239	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0002650	PMID:27623250	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001288	OMIM:618239	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0002376	PMID:27623250;PMID:30642748	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001260	PMID:27623250;PMID:30642748	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0002151	PMID:30642748	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0001263	OMIM:618239	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0011923	PMID:18614015;PMID:27623250;PMID:30642748	PCS		6/6			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0100874	PMID:27623250	PCS		1/1			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0011153	PMID:18614015	PCS		2/2			P	HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0002705	PMID:27623250	PCS		1/1			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:618239	Mitochondrial complex I deficiency, nuclear type 17		HP:0000007	PMID:18614015	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:616214	Hyperproinsulinemia		HP:0003074	OMIM:616214	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:616214	Hyperproinsulinemia		HP:0000842	OMIM:616214	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:616214	Hyperproinsulinemia		HP:0000006	PMID:3470784	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-11]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0004322	PMID:32917887	PCS		6/6			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001371	PMID:32917887	PCS		4/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000160	PMID:32917887	PCS		5/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0003593	PMID:32917887	PCS		2/5			C	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001290	PMID:32917887	PCS		5/6			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0045075	PMID:32917887	PCS		3/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0031107	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0006191	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0009064	PMID:32917887	PCS		4/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0011463	PMID:32917887	PCS		3/5			C	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0008897	PMID:32917887	PCS		6/6			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0002857	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0040217	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0005328	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001403	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0002155	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001387	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000097	PMID:32917887	PCS		3/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000093	PMID:32917887	PCS		3/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0005180	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0009771	PMID:32917887	PCS		3/7			P	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0010284	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000767	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000007	PMID:32917887	PCS					I	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0005815	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0008404	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001852	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000520	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000322	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000883	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001653	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000325	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000248	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001655	PMID:32917887	PCS	HP:0003577	1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000343	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0002680	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0002240	PMID:32917887	PCS		4/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0004382	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0008070	PMID:32917887	PCS		5/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0100864	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000418	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000938	PMID:32917887	PCS		3/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000414	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000218	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000972	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0002910	PMID:32917887	PCS		3/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001620	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001029	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000430	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000270	PMID:32917887	PCS		5/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0010575	PMID:32917887	PCS		2/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0005280	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0003819	PMID:32917887	PCS		1/7			C	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000668	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000348	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001712	PMID:32917887	PCS		3/7			P	HPO:probinson[2021-01-15];HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0002007	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000586	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0000347	PMID:32917887	PCS		5/7			P	HPO:probinson[2021-01-15]
OMIM:619127	Mandibuloacral dysplasia progeroid syndrome		HP:0001952	PMID:32917887	PCS		1/7			P	HPO:probinson[2021-01-15]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0003676	OMIM:239000	TAS					C	HPO:skoehler[2017-07-13]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000365	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0002684	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0004322	PMID:12124406	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0001552	OMIM:239000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0003155	PMID:12124406	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0001252	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0005792	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0003593	PMID:12124406	PCS		1/1			C	HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0004482	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0001270	OMIM:239000	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0005090	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000939	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0001508	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0011001	OMIM:239000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0003828	OMIM:239000	TAS					M	HPO:skoehler[2017-07-13]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000938	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0002757	OMIM:239000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0001324	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000256	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0003148	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0001102	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0003260	OMIM:23900	TAS					P	HPO:probinson[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0033355	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0002150	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0002194	PMID:12124406	PCS		1/1			P	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0031013	OMIM:239000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0003080	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0006480	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000407	OMIM:239000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0002808	OMIM:239000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0002905	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000546	OMIM:239000	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000007	PMID:12124406	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0006487	OMIM:239000	TAS					P	HPO:probinson[2009-02-17]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0200056	OMIM:239000	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0000488	OMIM:239000	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:239000	Paget disease of bone 5, juvenile-onset		HP:0002149	OMIM:239000	IEA					P	HPO:iea[2009-02-17]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0000670	PMID:19268275	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0002750	PMID:19268275	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0002099	PMID:19268275	PCS		4/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0001263	PMID:19268275	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0002240	PMID:19268275	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0003593	PMID:19268275	PCS		2/5			C	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0004395	OMIM:612714	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0002570	PMID:19268275	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0010972	PMID:19268275	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0003193	PMID:19268275	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0004490	PMID:19268275	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0001508	PMID:19268275	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0001738	PMID:19268275	PCS		4/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0000938	PMID:19268275	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0000007	PMID:19268275	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0000988	PMID:19268275	PCS		3/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0000952	PMID:19268275	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0001744	PMID:19268275	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-26]
OMIM:612714	Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarialhyperostosis		HP:0003623	PMID:19268275	PCS		3/5			C	HPO:probinson[2022-11-26]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000365	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000486	PMID:10807690	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000089	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0004322	PMID:10807690	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000122	OMIM:270400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002021	PMID:10807690;PMID:34349606	PCS		11/11			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002020	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001290	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS	HP:0003593				P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0003073	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000081	PMID:35305950	PCS		1/3			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0010569	PMID:35305950;PMID:30674241	PCS		4/4			P	HPO:probinson[2013-08-11];HPO:probinson[2022-08-23];HPO:skoehler[2012-10-17];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000518	PMID:10807690	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000639	PMID:10807690	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0007165	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001845	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000238	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0009623	PMID:9678700	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000752	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002019	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001840	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000996	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000358	ISBN-13:978-0721606156;PMID:30674241	PCS		11/11			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000252	PMID:10807690;PMID:30674241	PCS		11/11			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0006979	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002033	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0004691	PMID:35305950	PCS		3/3			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000808	PMID:30674241	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002827	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000007	OMIM:270400	TAS					I	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001338	PMID:30674241	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000403	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000369	PMID:30674241;PMID:34349606	PCS		2/2			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000126	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000187	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001397	PMID:30674241	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001276	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS	HP:0011463				P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000341	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0003577	PMID:35305950;PMID:30674241;PMID:34349606	PCS		6/6			C	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000343	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002089	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000463	PMID:10807690;PMID:30674241	PCS		11/11			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000062	PMID:35305950;PMID:34349606	PCS		2/5			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001272	PMID:23918729	PCS		2/55			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001153	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001394	PMID:30674241	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002240	PMID:30674241	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0100702	PMID:23918729	PCS		17/55			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001305	PMID:23918729	PCS		11/55			P	HPO:probinson[2009-10-20];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002013	PMID:10807690	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001162	PMID:10807690;PMID:34349606	PCS		11/11			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000193	PMID:35305950	PCS		1/3			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002251	PMID:9024558	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001680	PMID:9024558	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000074	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0010655	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0007099	PMID:23918729	PCS		2/55			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000508	PMID:10807690;PMID:30674241	PCS		11/11			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000107	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001558	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001830	PMID:10807690	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000347	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000104	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000742	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0007537	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001831	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000286	PMID:30674241	PCS		1/1			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002983	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000046	PMID:9024558	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002101	PMID:10807690	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001252	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0003270	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000718	OMIM:270400	TAS					P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000717	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000316	PMID:34349606	PCS		1/1			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000678	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001522	PMID:34349606	PCS		1/1			C	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002579	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001643	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001884	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001249	PMID:35305950	PCS		1/3			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002611	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001765	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000175	PMID:35305950;PMID:34349606	PCS		3/5			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000054	PMID:9024558	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001663	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002079	PMID:23918729	PCS					P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0011968	PMID:30674241	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000171	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001263	PMID:35305950;PMID:30674241	PCS		3/4			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002506	PMID:23918729	PCS		2/55			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000964	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000048	PMID:9024558	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000047	PMID:9024558	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000960	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0009778	PMID:9678700	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002283	PMID:23918729	PCS		5/55			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001508	PMID:10807690	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001629	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0005709	PMID:30674241;PMID:34349606	PCS		2/2			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0030043	OMIM:270400	TAS					P	HPO:skoehler[2015-01-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000813	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001623	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001744	PMID:30674241	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001622	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000431	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-05-01]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0003146	PMID:35305950;PMID:30674241;PMID:34349606	PCS		3/5			P	HPO:probinson[2009-10-20];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0030048	PMID:23918729	PCS		35/55			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001360	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0005280	PMID:34349606	PCS		1/1			P	HPO:probinson[2012-05-01];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000826	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS					P	HPO:probinson[2009-10-20]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001639	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000308	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000822	PMID:34349606	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0007333	ISBN-13:978-0721606156	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001511	PMID:35305950	PCS		3/4			P	HPO:probinson[2009-10-20];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001631	PMID:34349606	PCS		1/1			P	HPO:probinson[2012-04-24];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0001510	PMID:35305950	PCS		3/4			P	HPO:probinson[2009-10-20];HPO:probinson[2022-08-23]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0000028	PMID:9024558	PCS					P	HPO:probinson[2012-04-24]
OMIM:270400	Smith-Lemli-Opitz syndrome		HP:0002566	OMIM:270400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003323	OMIM:609452	TAS				HP:0012839	P	HPO:skoehler[2013-06-06]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003236	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003445	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003555	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0001271	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003584	OMIM:609452	TAS					C	HPO:skoehler[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0009063	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0009073	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0001638	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003736	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003715	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0000006	OMIM:609452	IEA					I	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0002600	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:609452	Myopathy, myofibrillar, 4		HP:0003458	OMIM:609452	IEA					P	HPO:iea[2009-02-17]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000286	PMID:34022130	PCS		1/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0002540	PMID:34022130	PCS		4/14			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000486	PMID:34022130	PCS		10/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001332	PMID:34022130	PCS		8/30			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0004322	PMID:34022130	PCS		11/14			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001250	PMID:34022130	PCS		7/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001272	PMID:34022130	PCS		7/13			P	HPO:probinson[2022-02-12];HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001252	PMID:34022130	PCS		1/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0002141	PMID:34022130	PCS		2/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0003593	PMID:34022130	PCS					C	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0033725	PMID:34022130	PCS		13/13			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000639	PMID:34022130	PCS		3/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0012471	PMID:34022130	PCS		15/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000316	PMID:34022130	PCS		2/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001647	PMID:34022130	PCS		2/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001347	PMID:34022130	PCS		15/15			P	HPO:probinson[2022-02-12];HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000252	PMID:34022130	PCS		11/13			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000692	PMID:34022130	PCS		5/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0002059	PMID:34022130	PCS		6/13			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001344	PMID:34022130	PCS		4/14			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000574	PMID:34022130	PCS		10/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000431	PMID:34022130	PCS		3/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000232	PMID:34022130	PCS		14/15			P	HPO:probinson[2022-02-12];HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000276	PMID:34022130	PCS		13/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000194	PMID:34022130	PCS		15/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001263	PMID:34022130	PCS		15/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0002493	PMID:34022130	PCS		15/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0002194	PMID:34022130	PCS		15/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0011400	PMID:34022130	PCS		12/13			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0100660	PMID:34022130	PCS		1/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000508	PMID:34022130	PCS		2/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000007	PMID:34022130	PCS					I	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0008366	PMID:34022130	PCS		3/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000664	PMID:34022130	PCS		10/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000322	PMID:34022130	PCS		8/11			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0001257	PMID:34022130	PCS		13/15			P	HPO:probinson[2022-02-12];HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0002445	PMID:34022130	PCS		1/15			P	HPO:probinson[2022-02-12]
OMIM:619641	Hengel-Maroofian-Schols syndrome		HP:0000687	PMID:34022130	PCS		4/15			P	HPO:probinson[2022-02-12]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0001265	PMID:8619529	PCS		8/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0003202	PMID:8619529	PCS				HP:0003676	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0001771	PMID:8619529	PCS		1/14			P	HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0003236	PMID:8619529	PCS		8/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0003376	PMID:8619529	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0003596	PMID:8619529	PCS		2/14			C	HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0003691	PMID:8619529	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0011712	PMID:8619529	PCS		1/14			P	HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0009054	PMID:8619529	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0006380	PMID:8619529	PCS		1/14			P	HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0034394	PMID:8619529	PCS		2/14			P	HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0007340	PMID:8619529	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0011462	PMID:8619529	PCS		12/14			C	HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0009027	PMID:8619529	PCS		13/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0002515	PMID:8619529	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0003715	OMIM:300695	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0003701	PMID:8619529	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-21]
OMIM:300695	Scapuloperoneal myopathy, X-linked dominant		HP:0001423	PMID:18179901	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-02-21]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0001022	OMIM:606952	IEA					P	HPO:skoehler[2015-01-27]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0005599	OMIM:606952	TAS					P	HPO:probinson[2013-03-02]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0000639	OMIM:606952	TAS					P	HPO:probinson[2013-03-02]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0001010	OMIM:606952	TAS					P	HPO:probinson[2013-03-02]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0000613	OMIM:606952	TAS					P	HPO:probinson[2013-03-02]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0000007	OMIM:606952	TAS					I	HPO:probinson[2013-01-09]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0007894	OMIM:606952	TAS					P	HPO:probinson[2013-03-02]
OMIM:606952	Albinism, oculocutaneous, type IB		HP:0000505	OMIM:606952	TAS					P	HPO:probinson[2013-03-02]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:0000252	OMIM:245450	IEA					P	HPO:iea[2009-02-17]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:0000494	OMIM:245450	IEA					P	HPO:iea[2009-02-17]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:0000023	OMIM:245450	IEA					P	HPO:iea[2009-02-17]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:0000007	OMIM:245450	IEA					I	HPO:iea[2009-02-17]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:0003648	OMIM:245450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:6000467	PMID:30931947	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:0000526	OMIM:245450	IEA					P	HPO:iea[2009-02-17]
OMIM:245450	D-lactic aciduria with susceptibility to gout		HP:0001249	OMIM:245450	IEA					P	HPO:iea[2009-02-17]
OMIM:619872	Immunodeficiency 101 (varicella zoster virus-specific)		HP:0005318	PMID:30211253	PCS	HP:0011462	2/2			P	HPO:probinson[2022-08-14]
OMIM:619872	Immunodeficiency 101 (varicella zoster virus-specific)		HP:0000006	PMID:30211253	PCS					I	HPO:probinson[2022-08-14]
OMIM:619872	Immunodeficiency 101 (varicella zoster virus-specific)		HP:0034319	PMID:30211253	PCS		2/2			P	HPO:probinson[2022-09-05]
OMIM:232800	Glycogen storage disease VII		HP:0003236	PMID:7513946	PCS		3/3			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0003573	PMID:7513946	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:6000359	PMID:6227635	PCS		3/3			P	HPO:probinson[2024-02-27]
OMIM:232800	Glycogen storage disease VII		HP:0012544	PMID:7513946	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0009020	PMID:14339001	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0011463	PMID:14339001;PMID:7513946	PCS		3/4			C	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0025435	PMID:7513946	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0001923	PMID:7513946	PCS		2/3			P	HPO:probinson[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0001324	OMIM:232800	TAS					P	HPO:probinson[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0000952	PMID:7513946	PCS		2/3			P	HPO:skoehler[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0003546	OMIM:232800;PMID:7513946	PCS		3/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-07];HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0003326	PMID:7513946	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0003621	PMID:7513946	PCS		1/3			C	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0003388	PMID:14339001	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0000790	PMID:7513946	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0001081	OMIM:232800	TAS					P	HPO:skoehler[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0009051	PMID:7513946	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0003738	PMID:7513946	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0001878	OMIM:232800	TAS					P	HPO:probinson[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0000007	PMID:2140573	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0030271	OMIM:232800	TAS					P	HPO:probinson[2015-01-31]
OMIM:232800	Glycogen storage disease VII		HP:0008305	PMID:14339001	PCS		1/1			P	HPO:probinson[2013-12-15];HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0003710	PMID:7513946	PCS		2/3			P	HPO:probinson[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0008967	PMID:14339001	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:232800	Glycogen storage disease VII		HP:0001997	OMIM:232800	TAS					P	HPO:skoehler[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0002149	OMIM:232800	TAS					P	HPO:probinson[2009-02-17]
OMIM:232800	Glycogen storage disease VII		HP:0003557	PMID:7513946	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:120502	Branchiootic syndrome 2		HP:0004467	OMIM:120502	TAS					P	HPO:skoehler[2009-02-17]
OMIM:120502	Branchiootic syndrome 2		HP:0000365	OMIM:120502	TAS					P	HPO:skoehler[2009-02-17]
OMIM:120502	Branchiootic syndrome 2		HP:0000377	OMIM:120502	TAS					P	HPO:skoehler[2012-08-01]
OMIM:120502	Branchiootic syndrome 2		HP:0000006	OMIM:120502	TAS					I	HPO:skoehler[2009-02-17]
OMIM:120502	Branchiootic syndrome 2		HP:0002710	OMIM:120502	TAS					P	HPO:skoehler[2009-02-17]
OMIM:208550	Asthma, nasal polyps, and aspirin intolerance		HP:0002099	OMIM:208550	IEA					P	HPO:iea[2009-02-17]
OMIM:208550	Asthma, nasal polyps, and aspirin intolerance		HP:0012042	OMIM:208550	TAS					P	HPO:probinson[2012-08-01]
OMIM:208550	Asthma, nasal polyps, and aspirin intolerance		HP:0000007	OMIM:208550	IEA					I	HPO:iea[2009-02-17]
OMIM:208550	Asthma, nasal polyps, and aspirin intolerance		HP:0100582	OMIM:208550	TAS					P	HPO:skoehler[2009-02-17]
OMIM:208550	Asthma, nasal polyps, and aspirin intolerance		HP:4000007	OMIM:208550	TAS				HP:0032365	P	HPO:probinson[2021-10-03]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0003566	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0002013	OMIM:241150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0000848	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0003394	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0001949	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0000007	OMIM:241150	IEA					I	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0002900	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0000114	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0002018	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0012378	OMIM:241150	TAS					P	HPO:skoehler[2013-10-22]
OMIM:241150	Hypokalemic alkalosis, familial, with specific renal tubulopathy		HP:0004921	OMIM:241150	IEA					P	HPO:iea[2009-02-17]
OMIM:603194	Meckel syndrome, type 2		HP:0000175	PMID:20512146	PCS		4/8			P	HPO:probinson[2013-03-23];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0002323	PMID:20512146	PCS		2/9			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0003577	PMID:20512146	PCS		5/8			C	HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0001162	PMID:20512146	PCS					P	HPO:skoehler[2015-04-26];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0002084	PMID:20512146	PCS		5/9			P	HPO:probinson[2013-03-23];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0010442	PMID:20512146	PCS		6/8			P	HPO:probinson[2013-03-23];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0001408	PMID:20512146	PCS		6/7			P	HPO:probinson[2013-03-23];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0011461	PMID:20512146	PCS		3/8			C	HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0000107	PMID:20512146	PCS		10/10			P	HPO:probinson[2013-03-23];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0000007	PMID:20512146	PCS					I	HPO:probinson[2013-01-09]
OMIM:603194	Meckel syndrome, type 2		HP:0000568	PMID:20512146	PCS		1/9			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0001305	PMID:20512146	PCS		1/9			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0006487	PMID:20512146	PCS		4/8			P	HPO:probinson[2013-03-23];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0001539	PMID:20512146	PCS		1/8			P	HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0001511	PMID:20512146	PCS		2/8			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0000476	PMID:20512146	PCS		1/8			P	HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0002566	PMID:20512146	PCS		1/8			P	HPO:probinson[2022-05-28]
OMIM:603194	Meckel syndrome, type 2		HP:0002435	PMID:20512146	PCS		5/9			P	HPO:probinson[2013-03-23];HPO:probinson[2022-05-28]
OMIM:613387	Fatty liver disease, nonalcoholic, susceptibility to, 2		HP:0001397	OMIM:613387	TAS					P	HPO:skoehler[2013-06-11]
OMIM:613387	Fatty liver disease, nonalcoholic, susceptibility to, 2		HP:0001426	OMIM:613387	TAS					I	HPO:probinson[2022-09-02]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0000121	PMID:15211439	PCS					P	HPO:probinson[2013-04-02]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0001254	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0025066	OMIM:611590	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0004322	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0000980	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0030036	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0008341	PMID:15211439	PCS					P	HPO:probinson[2013-04-02]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0001508	PMID:15211439	PCS					P	HPO:probinson[2013-04-02]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0004918	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0002748	PMID:15211439	PCS					P	HPO:probinson[2013-04-02]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0001878	OMIM:611590	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0000007	PMID:15211439	PCS					I	HPO:probinson[2013-01-09]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0002900	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0001923	OMIM:611590	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0001433	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0001942	PMID:15211439	PCS					P	HPO:probinson[2013-04-02]
OMIM:611590	Renal tubular acidosis, distal, with hemolytic anemia		HP:0002039	OMIM:611590	TAS					P	HPO:skoehler[2017-07-13]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003236	PMID:29079705	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003198	OMIM:255125	IEA					P	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001252	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003394	OMIM:255125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0002460	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001903	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0011463	PMID:29079705	PCS		1/1			C	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0002913	OMIM:255125	IEA					P	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0008314	PMID:29079705	PCS		1/1			P	HPO:skoehler[2012-11-26];HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001924	OMIM:255125	IEA					P	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0002359	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001324	OMIM:255125	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001962	OMIM:255125	IEA					P	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001488	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0000597	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003548	OMIM:255125	TAS					P	HPO:skoehler[2012-11-21]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003546	PMID:29079705	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003128	OMIM:255125	IEA					P	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003202	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003621	OMIM:255125	IEA					C	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001288	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003388	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001882	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003201	OMIM:255125	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0011924	PMID:29079705	PCS		1/1			P	HPO:skoehler[2012-11-26];HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0002151	OMIM:255125	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0001284	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0002094	OMIM:255125	IEA					P	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0011923	PMID:29079705	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0012240	OMIM:255125	IEA					P	HPO:probinson[2013-04-01]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0000007	PMID:29079705	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0008347	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003737	OMIM:255125	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0008306	OMIM:255125	IEA					P	HPO:iea[2009-02-17]
OMIM:255125	Myopathy with exercise intolerance, Swedish type		HP:0003557	PMID:29079705	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0001892	PMID:17110937	PCS		5/10			P	HPO:probinson[2013-04-01]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0001102	PMID:17110937	PCS		4/10			P	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0011858	PMID:17110937	PCS					P	HPO:probinson[2013-04-01]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0033027	PMID:17110937	PCS		2/9			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0008151	PMID:18800149	PCS					P	HPO:probinson[2019-01-21]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0008321	PMID:17110937	PCS					P	HPO:probinson[2013-04-01]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0011462	PMID:17110937	IEA					C	HPO:probinson[2020-07-20]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0008169	PMID:17110937	PCS					P	HPO:probinson[2013-04-01]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0000007	PMID:17110937	PCS					I	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0000421	PMID:17110937	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0025507	PMID:17110937	PCS		5/8			P	HPO:probinson[2020-07-20]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0002621	PMID:17110937	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0000973	PMID:17110937	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0001276	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0003577	PMID:18627047	PCS		1/1			C	HPO:probinson[2022-09-02]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0006808	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0001053	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0011379	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0011382	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0011381	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0000639	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0000957	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0000635	PMID:18627047	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-09-02]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0000458	OMIM:611584	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0001107	PMID:18627047	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-02]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0002617	OMIM:611584	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0002216	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0001249	OMIM:611584	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0001100	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0008936	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0002211	PMID:18627047	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-09-02]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0001263	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0011376	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0000407	PMID:18627047	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-09-02]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0000767	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0007894	PMID:18627047	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-09-02]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0007730	PMID:18627047	PCS		1/1			P	HPO:probinson[2022-09-02]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0007676	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0002227	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0000006	OMIM:611584	PCS					I	HPO:probinson[2012-04-11]
OMIM:611584	Waardenburg syndrome, type 2E		HP:0002226	OMIM:611584	PCS					P	HPO:probinson[2012-04-11]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003236	PMID:23313956	PCS		2/6		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0010628	OMIM:615084	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003676	PMID:23313956	PCS					C	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0001272	PMID:23313956	PCS		5/5			P	HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0011675	PMID:23313956	PCS		1/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0000815	OMIM:615084	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0002719	OMIM:615084	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0011462	PMID:23313956	PCS					C	HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0007126	OMIM:615084	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0002018	OMIM:615084	TAS		HP:0040283			P	HPO:skoehler[2013-02-25]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003306	PMID:23313956	PCS		2/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0001249	PMID:23313956	PCS		3/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0001644	PMID:23313956	PCS		1/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003546	PMID:23313956	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003700	PMID:23313956	PCS		5/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003689	PMID:23313956	PCS		6/6			P	HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0001265	PMID:23313956	PCS		2/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0000252	PMID:23313956	PCS		2/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003621	PMID:23313956	PCS					C	HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003200	PMID:23313956	PCS		6/6			P	HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0003388	OMIM:615084	TAS					P	HPO:skoehler[2013-02-25]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0000590	PMID:23313956	PCS		6/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0002094	PMID:23313956	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0002093	PMID:23313956	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0011923	PMID:23313956	PCS		4/4			P	HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0001618	PMID:23313956	PCS		2/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0002808	PMID:23313956	PCS		4/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0000508	PMID:23313956	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0000007	PMID:23313956	PCS					I	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0008443	PMID:23313956	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0008347	PMID:23313956	PCS		2/4			P	HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0001611	PMID:23313956	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2022-11-09]
OMIM:615084	Mitochondrial DNA depletion syndrome 11		HP:0002028	PMID:23313956	PCS		2/6			P	HPO:probinson[2022-11-09]
OMIM:612933	Glycogen storage disease XI		HP:0003236	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0003621	OMIM:612933	IEA					C	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0003552	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0003201	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0003542	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0000083	OMIM:612933	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612933	Glycogen storage disease XI		HP:0002063	OMIM:612933	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612933	Glycogen storage disease XI		HP:0002151	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0003394	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0002913	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0000007	OMIM:612933	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0003326	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612933	Glycogen storage disease XI		HP:0003546	OMIM:612933	IEA					P	HPO:skoehler[2010-06-19]
OMIM:185800	Symphalangism, proximal, 1A		HP:0010194	OMIM:185800	IEA		HP:0040283			P	HPO:iea[2010-01-20]
OMIM:185800	Symphalangism, proximal, 1A		HP:0000381	PMID:10080184	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:185800	Symphalangism, proximal, 1A		HP:0006152	PMID:32478388	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:185800	Symphalangism, proximal, 1A		HP:0005880	PMID:10080184	PCS		HP:0040284			P	HPO:iea[2010-01-20];HPO:probinson[2022-03-23]
OMIM:185800	Symphalangism, proximal, 1A		HP:0009843	OMIM:185800	IEA		HP:0040283			P	HPO:iea[2010-01-20]
OMIM:185800	Symphalangism, proximal, 1A		HP:0010047	OMIM:185800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:185800	Symphalangism, proximal, 1A		HP:0000405	PMID:10080184	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:185800	Symphalangism, proximal, 1A		HP:0008368	PMID:10080184	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:185800	Symphalangism, proximal, 1A		HP:0009702	PMID:10080184	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:185800	Symphalangism, proximal, 1A		HP:0000006	PMID:10080184	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-23]
OMIM:185800	Symphalangism, proximal, 1A		HP:0001204	PMID:10080184	PCS		HP:0040283			P	HPO:iea[2010-01-20];HPO:probinson[2022-03-23]
OMIM:173600	Pneumothorax, primary spontaneous		HP:0003829	OMIM:173600	IEA					I	HPO:iea[2009-02-17]
OMIM:173600	Pneumothorax, primary spontaneous		HP:0002108	OMIM:173600	TAS					P	HPO:skoehler[2015-01-21]
OMIM:173600	Pneumothorax, primary spontaneous		HP:0000006	OMIM:173600	IEA					I	HPO:iea[2009-02-17]
OMIM:415000	Spermatogenic failure, Y-linked, 2		HP:0001450	OMIM:415000	IEA					I	HPO:iea[2009-02-17]
OMIM:415000	SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED		HP:0003251	OMIM:415000	TAS					P	HPO:probinson[2022-07-20]
OMIM:415000	SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED		HP:0011462	OMIM:415000	TAS					C	HPO:probinson[2022-07-20]
OMIM:415000	Spermatogenic failure, Y-linked, 2		HP:0000027	OMIM:415000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:309100	Macular dystrophy, X-linked		HP:0001417	OMIM:309100	IEA					I	HPO:iea[2009-02-17]
OMIM:309100	Macular dystrophy, X-linked		HP:0007754	OMIM:309100	IEA					P	HPO:iea[2009-02-17]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0002069	PMID:31020005	PCS	HP:0011463	4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0000750	PMID:31020005	PCS		2/4			P	HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0001344	PMID:31020005	PCS		1/4			P	HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0001263	PMID:31020005	PCS					P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0003593	PMID:31020005	PCS		4/4			C	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0002080	PMID:31020005	PCS	HP:0003593	4/4			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0007018	PMID:31020005	PCS		1/4			P	HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0000006	PMID:31020005	PCS					I	HPO:probinson[2022-08-23]
OMIM:617863	Intellectual developmental disorder, autosomal dominant 69		HP:0001249	PMID:31020005	PCS		3/4			P	HPO:probinson[2022-08-23]
OMIM:619696	Spermatogenic failure 64		HP:0034011	PMID:30878252	PCS		2/2			P	HPO:probinson[2022-03-20]
OMIM:619696	Spermatogenic failure 64		HP:0003251	PMID:30878252	PCS		2/2			P	HPO:probinson[2022-03-20]
OMIM:619696	Spermatogenic failure 64		HP:0011462	PMID:30878252	PCS		2/2			C	HPO:probinson[2022-03-20]
OMIM:619696	Spermatogenic failure 64		HP:0000007	PMID:30878252	PCS					I	HPO:probinson[2022-03-20]
OMIM:619696	Spermatogenic failure 64		HP:0000798	PMID:30878252	PCS		2/2			P	HPO:probinson[2022-03-20]
OMIM:619696	Spermatogenic failure 64		HP:0012865	PMID:30878252	PCS		2/2			P	HPO:probinson[2022-03-20]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000483	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002540	PMID:37947183	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000486	PMID:37947183	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0004322	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000122	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001695	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002384	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0003593	PMID:37947183	PCS		15/18			C	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0003072	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012466	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012469	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000639	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000637	PMID:37947183	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0003228	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000358	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0003623	PMID:37947183	PCS		2/18			C	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0003763	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000252	PMID:37947183	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0033454	PMID:37947183	PCS		8/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001182	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0007270	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000767	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000007	PMID:37947183	PCS					I	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000520	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000369	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000248	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001733	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001336	PMID:37947183	PCS		5/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0025406	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000341	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000340	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0031728	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012448	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012332	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0020221	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000218	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001269	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000336	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000577	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001028	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001562	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001561	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000750	PMID:37947183	PCS		17/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002133	PMID:37947183	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001288	PMID:37947183	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002373	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000194	PMID:37947183	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0005487	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0010819	PMID:37947183	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0003065	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0025190	PMID:37947183	PCS		8/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000508	PMID:37947183	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001558	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000347	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001531	PMID:37947183	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001773	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000160	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001252	PMID:37947183	PCS		17/17			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001251	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0032794	PMID:37947183	PCS		8/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000280	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012389	PMID:37947183	PCS		0/17			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0045074	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012393	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0011463	PMID:37947183	PCS		1/18			C	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0011220	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001488	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0004756	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002751	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001385	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000175	PMID:37947183	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002870	PMID:37947183	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001662	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0011968	PMID:37947183	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002197	PMID:37947183	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001263	PMID:37947183	PCS		18/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002194	PMID:37947183	PCS		16/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000565	PMID:37947183	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001257	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000322	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0007359	PMID:37947183	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000445	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002169	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0004467	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002045	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001596	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000023	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000540	PMID:37947183	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0020152	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012408	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0010862	PMID:37947183	PCS		18/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0011675	PMID:37947183	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0012523	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002719	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002714	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000256	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002058	PMID:37947183	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0008936	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000272	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0400000	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0005280	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0032988	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000821	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000307	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0200055	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001873	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000545	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0002445	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0000303	PMID:37947183	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620771	Jeffries-Lakhani neurodevelopmental syndrome		HP:0001875	PMID:37947183	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:125320	Dementia/parkinsonism with non-alzheimer amyloid plaques		HP:0001300	OMIM:125320	TAS					P	HPO:skoehler[2009-02-17]
OMIM:125320	Dementia/parkinsonism with non-alzheimer amyloid plaques		HP:0000726	OMIM:125320	TAS				HP:0012828	P	HPO:skoehler[2009-02-17]
OMIM:125320	Dementia/parkinsonism with non-alzheimer amyloid plaques		HP:0011960	OMIM:125320	TAS					P	HPO:probinson[2012-07-28]
OMIM:125320	Dementia/parkinsonism with non-alzheimer amyloid plaques		HP:0000006	OMIM:125320	TAS					I	HPO:probinson[2009-02-17]
OMIM:189960	Tracheoesophageal fistula with or without esophageal atresia		HP:0002575	OMIM:189960	IEA					P	HPO:iea[2009-02-17]
OMIM:189960	Tracheoesophageal fistula with or without esophageal atresia		HP:0002032	OMIM:189960	IEA					P	HPO:iea[2009-02-17]
OMIM:209100	Atonic-Astatic syndrome of foerster		HP:0002540	OMIM:209100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:209100	Atonic-Astatic syndrome of foerster		HP:0012651	OMIM:209100	TAS					P	HPO:skoehler[2014-02-25]
OMIM:209100	Atonic-Astatic syndrome of foerster		HP:0001252	OMIM:209100	IEA					P	HPO:iea[2009-02-17]
OMIM:209100	Atonic-Astatic syndrome of foerster		HP:0001251	OMIM:209100	IEA					P	HPO:iea[2009-02-17]
OMIM:209100	Atonic-Astatic syndrome of foerster		HP:0001290	OMIM:209100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:209100	Atonic-Astatic syndrome of foerster		HP:0000007	OMIM:209100	IEA					I	HPO:iea[2009-02-17]
OMIM:515000	Chloramphenicol toxicity		HP:0001915	OMIM:515000	IEA					P	HPO:iea[2009-02-17]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0008947	OMIM:617877	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000341	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000343	PMID:29198724	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0004763	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000463	PMID:29198724	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0004322	PMID:29198724	PCS		8/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0003298	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0003196	PMID:29198724	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001252	PMID:29198724	PCS		3/11			P	HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0010047	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0011675	PMID:29198724	PCS		3/9			P	HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0009102	PMID:29198724	PCS		5/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0011682	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000938	PMID:29198724	PCS		1/6			P	HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001669	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000337	PMID:29198724	PCS		8/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000678	PMID:29198724	PCS		6/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000219	OMIM:617877	IEA		10/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000878	PMID:29198724	PCS		6/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000218	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001642	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000358	PMID:29198724	PCS		7/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001249	PMID:29198724	PCS		0/11			P	HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000494	PMID:29198724	PCS		3/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0003302	PMID:29198724	PCS		3/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0002870	PMID:29198724	PCS		4/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0002750	OMIM:617877	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000232	PMID:29198724	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0011800	PMID:29198724	PCS		11/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0100797	PMID:29198724	PCS		3/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000767	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0004209	PMID:29198724	PCS		4/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000405	PMID:29198724	PCS		4/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000884	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001852	PMID:29198724	PCS		8/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000664	PMID:29198724	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000201	PMID:29198724	PCS		3/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000006	PMID:29198724	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0000369	OMIM:617877	IEA		7/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617877	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies		HP:0001831	OMIM:617877	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608957	Cd8 deficiency, familial		HP:0003577	OMIM:608957	TAS					C	HPO:probinson[2009-02-17]
OMIM:608957	Cd8 deficiency, familial		HP:0005422	OMIM:608957	TAS					P	HPO:probinson[2009-02-17]
OMIM:608957	Cd8 deficiency, familial		HP:0002110	OMIM:608957	TAS					P	HPO:probinson[2009-02-17]
OMIM:608957	Cd8 deficiency, familial		HP:0002718	OMIM:608957	TAS					P	HPO:probinson[2009-02-17]
OMIM:608957	Cd8 deficiency, familial		HP:0000007	OMIM:608957	TAS					I	HPO:probinson[2009-02-17]
OMIM:608957	Cd8 deficiency, familial		HP:0004429	OMIM:608957	TAS					P	HPO:probinson[2012-07-18]
OMIM:608957	Cd8 deficiency, familial		HP:0002205	OMIM:608957	TAS					P	HPO:skoehler[2010-06-20]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002960	OMIM:240500	TAS					P	HPO:probinson[2012-05-06]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002664	OMIM:240500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002240	OMIM:240500	TAS					P	HPO:probinson[2012-05-06]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0011839	PMID:16007086	PCS		0/5			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002718	OMIM:240500	TAS					P	HPO:probinson[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002716	OMIM:240500	IEA					P	HPO:iea[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002837	PMID:16007086	PCS		5/5			P	HPO:probinson[2012-05-06];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0006532	OMIM:240500	TAS					P	HPO:probinson[2012-05-06]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0001744	OMIM:240500	IEA					P	HPO:iea[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0004315	PMID:16007086	PCS		4/5			P	HPO:probinson[2009-02-17];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0001287	OMIM:240500	IEA					P	HPO:iea[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002014	OMIM:240500	IEA					P	HPO:iea[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002850	PMID:16007086	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0410301	PMID:16007086	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002110	OMIM:240500	IEA					P	HPO:iea[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0005387	PMID:16007086	PCS		5/5			P	HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0011840	OMIM:240500	IEA					P	HPO:iea[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0011108	PMID:16007086	PCS		5/5			P	HPO:probinson[2012-05-06];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0000509	OMIM:240500	IEA					P	HPO:iea[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002729	OMIM:240500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0000007	PMID:18981294	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0000403	PMID:16007086	PCS		5/5			P	HPO:probinson[2012-05-06];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0000006	PMID:16007086	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002665	OMIM:240500	TAS					P	HPO:probinson[2009-02-17]
OMIM:240500	Immunodeficiency, common variable, 2		HP:0002720	PMID:16007086	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2021-05-09]
OMIM:143890	Hypercholesterolemia, familial, 1		HP:0001084	OMIM:143890	TAS					P	HPO:skoehler[2014-06-24]
OMIM:143890	Hypercholesterolemia, familial, 1		HP:0003141	PMID:1301956	PCS					P	HPO:probinson[2020-11-26]
OMIM:143890	Hypercholesterolemia, familial, 1		HP:0010874	PMID:1301956	PCS					P	HPO:probinson[2020-11-26]
OMIM:143890	Hypercholesterolemia, familial, 1		HP:0000007	PMID:1301956	PCS					I	HPO:probinson[2020-11-26]
OMIM:143890	Hypercholesterolemia, familial, 1		HP:0001114	PMID:1301956	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2020-11-26]
OMIM:143890	Hypercholesterolemia, familial, 1		HP:0000006	PMID:1301956	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-11-26]
OMIM:143890	Hypercholesterolemia, familial, 1		HP:0001677	PMID:1301956	PCS					P	HPO:probinson[2020-11-26]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0002069	PMID:22713812	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0003621	PMID:22713812	PCS		3/13			C	HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0001250	PMID:22713812	PCS		7/13			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0003680	PMID:22713812	PCS					C	HPO:skoehler[2013-04-02];HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0001340	PMID:22713812	PCS		11/11			P	HPO:skoehler[2013-04-02];HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0001351	PMID:22713812	PCS		2/2			P	HPO:skoehler[2013-04-02];HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0011462	PMID:22713812	PCS		10/13			C	HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0002392	PMID:22713812	PCS		7/10			P	HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0000006	PMID:31539032	PCS					I	HPO:skoehler[2013-04-02];HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0001337	PMID:22713812	PCS		13/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0001249	PMID:22713812	PCS		0/13			P	HPO:probinson[2023-02-12]
OMIM:615127	Epilepsy, familial adult myoclonic, 4		HP:0001336	PMID:22713812	PCS		13/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:190410	Trigger thumb		HP:0001172	OMIM:190410	TAS					P	HPO:skoehler[2009-02-17]
OMIM:190410	Trigger thumb		HP:0000006	OMIM:190410	TAS					I	HPO:skoehler[2013-05-29]
OMIM:607523	Nail disorder, nonsyndromic congenital, 8		HP:0000006	PMID:11843659	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2019-04-20]
OMIM:607523	Nail disorder, nonsyndromic congenital, 8		HP:0001810	PMID:11843659	PCS					P	HPO:probinson[2019-04-20]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001034	PMID:28805828	PCS		1/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0003774	PMID:28805828	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0003577	PMID:28805828	PCS		2/4			C	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000100	PMID:28805828	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0004322	PMID:28805828	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001250	PMID:28805828	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001252	PMID:28805828	PCS		3/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0003593	PMID:28805828	PCS		2/4			C	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000316	PMID:28805828	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0100729	PMID:28805828	PCS		1/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0008677	PMID:28805828	PCS		2/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001967	PMID:28805828	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000411	PMID:28805828	PCS		1/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001249	PMID:28805828	PCS		1/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0002059	PMID:28805828	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000750	PMID:28805828	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001321	PMID:28805828	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0002057	PMID:28805828	PCS		1/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-04-04]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0011968	PMID:28805828	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001263	PMID:28805828	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000097	PMID:28805828	PCS		1/4			P	HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000093	PMID:28805828	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001182	OMIM:617730	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0011451	PMID:28805828	PCS		4/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-04-04]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000007	PMID:28805828	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0000505	OMIM:617730	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001357	PMID:28805828	PCS		1/4			P	HPO:probinson[2023-01-14];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0001257	PMID:28805828	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617730	Galloway-Mowat syndrome 4		HP:0002126	PMID:28805828	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003378	OMIM:601152	TAS					P	HPO:probinson[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003431	OMIM:601152	IEA				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003376	PMID:16437557	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003693	OMIM:601152	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0002460	PMID:16437557	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003593	OMIM:601152	TAS					C	HPO:probinson[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000360	OMIM:601152	IEA					P	HPO:iea[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003690	PMID:16437557	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0011463	PMID:16437557	PCS		8/10			C	HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0002938	PMID:16437557	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000458	OMIM:601152	IEA					P	HPO:iea[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0002936	PMID:16437557	PCS		10/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003409	PMID:16437557	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0001604	PMID:16437557	PCS		4/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003701	PMID:16437557	PCS		10/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0001265	PMID:16437557	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0007924	OMIM:601152	IEA					P	HPO:probinson[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0003621	PMID:16437557	PCS		2/10			C	HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0002650	PMID:16437557	PCS		1/10			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000551	OMIM:601152	TAS					P	HPO:skoehler[2013-01-22]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0001761	PMID:16437557	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0001284	OMIM:601152	IEA					P	HPO:iea[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000649	OMIM:601152	IEA					P	HPO:iea[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0008587	PMID:16437557	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000648	PMID:16437557	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000603	OMIM:601152	IEA					P	HPO:iea[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000543	PMID:16437557	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0002403	OMIM:601152	IEA					P	HPO:iea[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000641	OMIM:601152	IEA					P	HPO:iea[2009-02-17]
OMIM:601152	Hereditary motor and sensory neuropathy VIA		HP:0000006	PMID:16437557	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:235000	Hemihyperplasia, isolated		HP:0002650	OMIM:235000	IEA					P	HPO:iea[2009-02-17]
OMIM:235000	Hemihyperplasia, isolated		HP:0002475	OMIM:235000	TAS					P	HPO:probinson[2009-02-17]
OMIM:235000	Hemihyperplasia, isolated		HP:0003829	OMIM:235000	IEA					I	HPO:iea[2009-02-17]
OMIM:235000	Hemihyperplasia, isolated		HP:0001528	OMIM:235000	IEA					P	HPO:iea[2009-02-17]
OMIM:235000	Hemihyperplasia, isolated		HP:0002667	OMIM:235000	TAS					P	HPO:probinson[2009-02-17]
OMIM:235000	Hemihyperplasia, isolated		HP:0002898	OMIM:235000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:235000	Hemihyperplasia, isolated		HP:0003712	OMIM:235000	TAS					P	HPO:probinson[2009-02-17]
OMIM:235000	Hemihyperplasia, isolated		HP:0000006	OMIM:235000	IEA					I	HPO:iea[2009-02-17]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0002322	PMID:20629132	PCS		5/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0003621	PMID:20629132	PCS		1/5			C	HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0002067	PMID:20629132	PCS		4/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0001300	PMID:20629132	PCS		5/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0003596	PMID:20629132	PCS		3/5			C	HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0003487	PMID:20629132	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0002396	PMID:20629132	PCS		5/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0025709	PMID:20629132	PCS		1/5			C	HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0001419	PMID:20629132	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0000338	PMID:20629132	PCS		4/5			P	HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0001257	PMID:20629132	PCS		5/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0003677	PMID:20629132	PCS					C	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:300911	Parkinsonism with spasticity, X-linked		HP:0001347	PMID:20629132	PCS		3/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-25]
OMIM:601634	Neural tube defects, folate-sensitive		HP:0001939	OMIM:601634	IEA					P	HPO:iea[2009-02-17]
OMIM:601634	Neural tube defects, folate-sensitive		HP:0010301	OMIM:601634	TAS					P	HPO:skoehler[2015-01-21]
OMIM:601634	Neural tube defects, folate-sensitive		HP:0000007	OMIM:601634	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001177	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0002089	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0005873	OMIM:263520	TAS					P	HPO:probinson[2012-06-09]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000540	OMIM:263520	IEA					P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001156	OMIM:263520	IEA					P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000062	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000161	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001395	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0010984	OMIM:263520	TAS					I	HPO:probinson[2015-02-22]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001270	OMIM:263520	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001629	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001789	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001302	OMIM:263520	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000774	OMIM:263520	TAS					P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000113	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000773	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000556	OMIM:263520	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0005349	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001600	OMIM:263520	TAS					P	HPO:probinson[2015-02-22]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001320	OMIM:263520	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0005766	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0003026	OMIM:263520	TAS					P	HPO:probinson[2015-02-22]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000054	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0006956	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000175	OMIM:263520	TAS					P	HPO:probinson[2015-02-22]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0003027	OMIM:263520	IEA					P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000750	OMIM:263520	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001162	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000171	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0011802	OMIM:263520	TAS					P	HPO:probinson[2015-02-22]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0005180	OMIM:263520	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0100732	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000926	OMIM:263520	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000888	OMIM:263520	TAS					P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000007	OMIM:263520	TAS					I	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0005817	OMIM:263520	TAS					P	HPO:probinson[2009-02-17]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000768	OMIM:263520	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0001631	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0006644	OMIM:263520	IEA					P	HPO:skoehler[2015-01-27]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0002566	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		HP:0000248	OMIM:263520	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003774	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003676	PMID:27392076	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0004322	PMID:33185949;PMID:27392076	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-07-19];ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0012606	PMID:33185949;PMID:27392076	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0020132	PMID:27392076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003593	PMID:33185949	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0040084	PMID:27392076	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0040085	PMID:27392076	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0012622	PMID:33185949;PMID:27392076	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-19];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0032218	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0002719	PMID:33185949;PMID:27392076	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-07-19];ORCID:0000-0002-0736-9199[2024-07-19];HPO:probinson[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001903	PMID:27392076	PCS	HP:0003577	5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001903	PMID:33185949	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0011463	PMID:27392076	PCS		2/4			C	HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0011342	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0011462	PMID:27392076	PCS		1/4			C	HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0012450	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0004719	PMID:27392076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000278	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003623	PMID:27392076	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0004732	PMID:33185949;PMID:27392076	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001562	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000110	PMID:27392076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003621	PMID:27392076	PCS		1/3			C	HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000112	PMID:27392076	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001882	PMID:27392076	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003165	PMID:33185949	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0002153	PMID:33185949;PMID:27392076	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0002572	PMID:33185949	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003584	PMID:27392076	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000097	PMID:27392076	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000790	PMID:27392076	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000093	PMID:33185949;PMID:27392076	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0034886	PMID:27392076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0012213	PMID:33185949;PMID:27392076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001919	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001518	PMID:33185949;PMID:27392076	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000822	PMID:27392076	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000107	PMID:27392076	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0004727	PMID:33185949	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0100838	PMID:27392076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001511	PMID:27392076	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000006	PMID:27392076	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003259	PMID:33185949;PMID:27392076	PCS		6/6			P	HPO:probinson[2023-02-21];ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001997	PMID:33185949;PMID:27392076	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-19];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0003138	PMID:33185949;PMID:27392076	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0000325	PMID:33185949;PMID:27392076	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-19]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0002149	PMID:33185949;PMID:27392076	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-19];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:617056	Tubulointerstitial kidney disease, autosomal dominant, 5		HP:0001875	PMID:33185949;PMID:27392076	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-19];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:613224	Noonan syndrome 6		HP:0000286	OMIM:613224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613224	Noonan syndrome 6		HP:0004523	OMIM:613224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613224	Noonan syndrome 6		HP:0000483	PMID:26467218	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000563	PMID:26467218	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000486	PMID:26467218	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0004322	PMID:26467218	PCS		5/14			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0001290	OMIM:613224	IEA		HP:0040280			P	HPO:skoehler[2013-01-10]
OMIM:613224	Noonan syndrome 6		HP:0000957	PMID:26467218	PCS		5/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0011461	PMID:26467218	PCS		4/14			C	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000316	PMID:26467218	PCS		14/14			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0001488	PMID:26467218	IEA		2/2			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0001642	PMID:26467218	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000358	PMID:26467218	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000494	PMID:26467218	PCS		14/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0011968	PMID:26467218	PCS		1/2			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0000969	OMIM:613224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613224	Noonan syndrome 6		HP:0000407	OMIM:613224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613224	Noonan syndrome 6		HP:0000767	PMID:26467218	PCS		9/13			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000766	PMID:19966803	PCS		4/5			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0000006	PMID:19966803	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0000369	OMIM:613224	IEA		14/14			P	HPO:skoehler[2013-01-10]
OMIM:613224	Noonan syndrome 6		HP:0001655	PMID:26467218	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0003577	PMID:26467218	PCS		10/14			C	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0001195	PMID:26467218	PCS	HP:0003577	1/10			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0002162	PMID:26467218	PCS		2/2			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0001270	PMID:26467218	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0012209	PMID:26467218	PCS		1/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0008070	PMID:19966803	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0000337	PMID:26467218	PCS		1/2			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0000978	PMID:26467218	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000256	PMID:26467218	PCS		5/13			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0006699	PMID:26467218	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0002212	PMID:26467218	PCS		5/11			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0001561	PMID:26467218	PCS	HP:0011461	4/10			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000750	PMID:19966803	PCS		1/5			P	HPO:skoehler[2013-01-10];HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0001003	PMID:26467218	PCS		2/2			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0000431	OMIM:613224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613224	Noonan syndrome 6		HP:0001680	PMID:26467218	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000470	PMID:26467218	PCS		2/2			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0005280	OMIM:613224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613224	Noonan syndrome 6		HP:0032152	PMID:26467218	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0001639	PMID:26467218	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000508	PMID:26467218	PCS		3/14			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000348	PMID:26467218	PCS		14/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-05-21]
OMIM:613224	Noonan syndrome 6		HP:0001631	PMID:26467218	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0001510	PMID:26467218	PCS		1/2			P	HPO:probinson[2021-05-19]
OMIM:613224	Noonan syndrome 6		HP:0000465	PMID:26467218	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000028	PMID:26467218	PCS		6/9	MALE		P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:613224	Noonan syndrome 6		HP:0000545	PMID:26467218	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:155980	Membranous cranial ossification, delayed		HP:0000494	OMIM:155980	TAS					P	HPO:skoehler[2015-07-05]
OMIM:155980	Membranous cranial ossification, delayed		HP:0000316	OMIM:155980	TAS					P	HPO:skoehler[2015-07-05]
OMIM:155980	Membranous cranial ossification, delayed		HP:0000348	OMIM:155980	TAS					P	HPO:skoehler[2017-07-13]
OMIM:155980	Membranous cranial ossification, delayed		HP:0002007	OMIM:155980	TAS					P	HPO:skoehler[2015-07-05]
OMIM:155980	Membranous cranial ossification, delayed		HP:0005280	OMIM:155980	TAS					P	HPO:skoehler[2015-07-05]
OMIM:155980	Membranous cranial ossification, delayed		HP:0000369	OMIM:155980	TAS					P	HPO:skoehler[2015-07-05]
OMIM:155980	Membranous cranial ossification, delayed		HP:0000006	OMIM:155980	TAS					I	HPO:skoehler[2015-12-30]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009816	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000483	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0001773	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000486	PMID:10080184	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0008607	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0006077	PMID:15770128	PCS		2/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0005807	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000954	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009466	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000879	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009941	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009702	OMIM:186500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0005104	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0004691	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0010554	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0003083	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009295	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009177	PMID:15770128	PCS		2/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009773	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0006385	OMIM:186500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000646	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000767	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000920	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0004209	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000405	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0008368	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000322	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000006	PMID:10080184	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0011918	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000582	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0001156	OMIM:186500	TAS					P	HPO:skoehler[2014-11-26]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000540	PMID:15770128	PCS		4/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0010109	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000381	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0004220	PMID:15770128	PCS		2/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0005792	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0100394	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0010624	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000219	PMID:10080184	PCS		4/5			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0002515	PMID:10080184	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0008513	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000215	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000275	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000431	PMID:15770128	PCS		3/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000430	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0003022	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0100482	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0100481	PMID:15770128	PCS		1/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0008460	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0000508	PMID:15770128	PCS		2/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0009477	PMID:15770128	PCS		2/5			P	HP:probinson[2022-02-19]
OMIM:186500	Multiple synostoses syndrome 1		HP:0002967	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0003416	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:186500	Multiple synostoses syndrome 1		HP:0001798	OMIM:186500	IEA					P	HPO:iea[2009-02-17]
OMIM:620836	Immunodeficiency 120		HP:0002850	PMID:31449058;PMID:31629014	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0006889	PMID:31449058;PMID:31629014	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0000252	PMID:31449058	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0000365	PMID:31449058;PMID:31629014	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0000750	PMID:31629014	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0002783	PMID:31449058;PMID:31629014	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0004322	PMID:31449058	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0002110	PMID:31449058	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0410295	PMID:31629014	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0003593	PMID:31629014	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0010976	PMID:31449058	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0032218	PMID:31449058;PMID:31629014	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0000407	PMID:31629014	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0011463	PMID:31629014	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0032275	PMID:31449058;PMID:31629014	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0002788	PMID:31449058;PMID:31629014	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0200043	PMID:31449058	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0410028	PMID:31449058;PMID:31629014	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0002720	PMID:31449058;PMID:31629014	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0000006	PMID:31449058	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0004315	PMID:31449058;PMID:31629014	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0040218	PMID:31449058	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620836	Immunodeficiency 120		HP:0004469	PMID:31449058	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:618371	Turnpenny-Fry syndrome		HP:0004325	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000164	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002389	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000160	PMID:30343942	PCS		7/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001252	PMID:30343942	PCS		5/13			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001054	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002020	PMID:30343942	PCS		6/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0004482	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002938	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001845	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001328	PMID:25533962	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000678	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0100807	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000879	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001643	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002019	PMID:25533962;PMID:30343942	PCS		3/15			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0006237	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001249	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000995	PMID:25533962	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0003502	PMID:25533962	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000297	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000494	PMID:25533962	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000252	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002870	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001344	PMID:30343942	PCS		3/13			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0005302	PMID:30343942	PCS		2/13			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002750	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002079	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001382	PMID:25533962	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001260	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001263	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000691	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001182	PMID:25533962	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001181	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000729	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000767	PMID:30343942	PCS		2/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000689	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0100818	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001659	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000405	PMID:30343942	PCS		6/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002307	PMID:25533962	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000768	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0005659	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000006	PMID:25533962	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000248	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000369	OMIM:618371	IEA		10/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000687	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0030676	PMID:30343942	PCS		11/13			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000260	PMID:30343942	PCS		1/13			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0005274	PMID:30343942	PCS		10/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001508	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0012450	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0008551	PMID:25533962;PMID:30343942	PCS		8/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000337	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0008872	PMID:30343942	PCS		6/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000219	PMID:30343942	PCS		5/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001704	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0030084	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002714	PMID:30343942	PCS		3/13			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000218	PMID:30343942	PCS		4/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0006334	PMID:25533962	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000774	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000256	PMID:25533962	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0008936	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001320	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000473	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001561	PMID:30343942	PCS		5/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000276	PMID:25533962;PMID:30343942	PCS		7/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001761	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000272	OMIM:618371	IEA		10/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0045025	PMID:30343942	PCS		5/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000629	PMID:30343942	PCS		9/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002209	PMID:30343942	PCS		3/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002007	PMID:25533962;PMID:30343942	PCS		12/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001511	PMID:30343942	PCS		3/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001357	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0002205	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0200055	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001631	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618371	Turnpenny-Fry syndrome		HP:0007018	PMID:30343942	PCS		2/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0000303	PMID:25533962;PMID:30343942	PCS		5/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618371	Turnpenny-Fry syndrome		HP:0001634	OMIM:618371	IEA					P	HPO:skoehler[2019-09-07]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0002037	OMIM:106300	TAS					P	HPO:skoehler[2012-10-12]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0012317	OMIM:106300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0011675	OMIM:106300	TAS					P	HPO:probinson[2009-02-17]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0012122	OMIM:106300	TAS					P	HPO:skoehler[2012-10-12]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0100686	OMIM:106300	TAS					P	HPO:skoehler[2012-10-12]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0040313	OMIM:106300	TAS					P	HPO:probinson[2020-07-06]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0002808	OMIM:106300	TAS					P	HPO:skoehler[2010-06-20]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0001426	OMIM:106300	TAS					I	HPO:skoehler[2010-06-19]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0001659	OMIM:106300	TAS					P	HPO:probinson[2009-02-17]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0003418	OMIM:106300	TAS					P	HPO:skoehler[2010-06-20]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0002923	PMID:7702399	PCS		0/7			P	HPO:probinson[2015-01-31];HPO:probinson[2024-03-08]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0008843	OMIM:106300	TAS					P	HPO:iea[2009-02-17]
OMIM:106300	Spondyloarthropathy, susceptibility to, 1		HP:0003765	OMIM:106300	TAS					P	HPO:probinson[2009-02-17]
OMIM:182000	Keratosis, seborrheic, somatic		HP:0010816	PMID:17673550	PCS					P	HPO:probinson[2020-07-21]
OMIM:182000	Keratosis, seborrheic, somatic		HP:0001442	PMID:17673550	PCS					I	HPO:probinson[2020-07-21]
OMIM:182000	Keratosis, seborrheic, somatic		HP:0031287	PMID:17673550	PCS					P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0002378	PMID:23297365	PCS		4/5	MALE		P	HPO:skoehler[2013-10-06];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0002378	PMID:25864721	PCS		6/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0030237	PMID:23297365	PCS		5/5	MALE		P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0003621	PMID:23297365	PCS		3/5	MALE		C	HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0003621	PMID:25864721	PCS		2/4	FEMALE		C	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0003376	PMID:23297365	PCS		5/5	MALE		P	HPO:skoehler[2013-10-06];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0003596	PMID:25864721	PCS		2/4	FEMALE		C	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0001761	PMID:23297365	PCS		5/5	MALE		P	HPO:skoehler[2013-10-06];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0001761	PMID:25864721	PCS		2/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0009072	PMID:25864721	PCS		1/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0000407	PMID:23297365	PCS		1/5	MALE		P	HPO:skoehler[2013-10-06];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0011463	PMID:23297365	PCS		2/5	MALE		C	HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0009830	PMID:23297365	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0001423	PMID:23297365	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0008954	PMID:23297365	PCS		2/5	MALE		P	HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0008954	PMID:25864721	PCS		5/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0003438	PMID:23297365	PCS		5/5	MALE		P	HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0003438	PMID:25864721	PCS		3/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0006886	PMID:23297365	PCS		5/5	MALE		P	HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0006886	PMID:25864721	PCS		2/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0003677	PMID:23297365	PCS					C	HPO:skoehler[2013-10-06];HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0007328	PMID:23297365	PCS		5/5	MALE		P	HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0007328	PMID:25864721	PCS		0/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0008944	PMID:23297365	PCS		5/5	MALE		P	HPO:probinson[2023-01-17]
OMIM:300905	Charcot-Marie-Tooth disease, X-linked dominant, 6		HP:0008944	PMID:25864721	PCS		4/8	FEMALE		P	HPO:probinson[2023-01-18]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000343	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001212	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001795	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000365	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0004322	PMID:33268356	PCS		4/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0002020	PMID:33268356	PCS		4/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0003593	PMID:33268356	PCS					C	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0004383	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0008070	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001508	PMID:33268356	PCS		4/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0011220	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0012450	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001548	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001647	PMID:33268356	PCS		0/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0009765	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0002857	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000256	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001763	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001601	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001166	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000252	PMID:33268356	PCS		8/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0002650	PMID:33268356	PCS		4/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001761	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0005487	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001382	PMID:33268356	PCS		0/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001263	PMID:33268356	PCS		12/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0011800	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001182	PMID:33268356	PCS		3/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0011304	PMID:33268356	PCS		0/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0100259	PMID:33268356	PCS		0/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000348	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000964	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0004209	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0008467	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001357	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000268	PMID:33268356	PCS		2/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0002007	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0001631	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000006	PMID:33268356	PCS					I	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000248	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:619721	Bryant-Li-Bhoj neurodevelopmental syndrome 2		HP:0000303	PMID:33268356	PCS		1/13			P	HPO:probinson[2022-05-09]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001771	OMIM:612674	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001310	OMIM:612674	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001272	PMID:20797687	PCS		7/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0003693	OMIM:612674	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001251	PMID:20797687	PCS		12/19			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0002080	PMID:20797687	PCS		2/19			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000639	OMIM:612674	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0007141	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000518	PMID:20797687	PCS		15/19			P	HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0011463	PMID:20797687	PCS		5/18			C	HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0011462	PMID:20797687	PCS		7/18			C	HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0002936	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000510	PMID:20797687	PCS		7/19			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001347	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0007108	PMID:20797687	PCS		11/12			P	HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001265	PMID:20797687	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0003621	PMID:20797687	PCS		6/18			C	HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0003487	PMID:20797687	PCS		10/19			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001761	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001260	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000407	PMID:20797687	PCS		19/19			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000007	PMID:20797687	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000648	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000762	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0001257	PMID:20797687	PCS		4/19			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0003677	PMID:20797687	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-04]
OMIM:612674	Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract		HP:0000523	OMIM:612674	IEA					P	HPO:skoehler[2010-06-19]
OMIM:614205	3-M syndrome 3		HP:0004325	PMID:21737058	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000343	PMID:21737058	PCS		1/6			P	HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000463	PMID:21737058	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0004322	PMID:21737058	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0005274	PMID:21737058	PCS		6/6			P	HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0012428	PMID:21737058	PCS		6/6			P	HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0010306	PMID:21737058	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0012471	PMID:21737058	PCS		2/6			P	HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0003307	PMID:21737058	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000411	PMID:21737058	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0001385	PMID:21737058	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000252	PMID:21737058	PCS		1/3			P	HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0001382	PMID:21737058	PCS		1/6			P	HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0003100	PMID:21737058	PCS		2/6			P	HPO:skoehler[2013-05-31];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000470	PMID:21737058	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0004570	PMID:21737058	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0011800	PMID:21737058	PCS		3/6			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0001518	PMID:21737058	PCS	HP:0003577	6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000007	PMID:21737058	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000307	PMID:21737058	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0004209	PMID:21737058	PCS		1/6			P	HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000268	PMID:21737058	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0002007	PMID:21737058	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0001510	PMID:21737058	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
OMIM:614205	3-M syndrome 3		HP:0000325	PMID:21737058	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-07]
DECIPHER:67	1q21.1 recurrent microduplication (possible susceptibility locus for neurodevelopmental disorders)		HP:0000717	DECIPHER:67	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:67	1q21.1 recurrent microduplication (possible susceptibility locus for neurodevelopmental disorders)		HP:0001249	DECIPHER:67	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0003477	PMID:21076407	PCS		3/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001773	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0002365	PMID:23603762	PCS		2/11			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001250	PMID:21076407	PCS		7/8			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001252	PMID:21076407	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0003593	PMID:21076407	PCS		1/1			C	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0011220	PMID:21076407	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0002515	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001769	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001302	PMID:21076407	PCS		9/11			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001169	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001249	PMID:23603762	PCS		6/11			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0000297	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001265	PMID:21076407	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001320	PMID:23603762	PCS		3/11			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0000494	PMID:21076407	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0000252	PMID:21076407	PCS		3/8			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0002510	PMID:21076407	PCS		3/8			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0004279	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001288	OMIM:614563	TAS					P	HPO:probinson[2013-08-10]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0002079	PMID:23603762	PCS		7/11			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001263	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0032046	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0030051	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0001357	PMID:21076407	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0007359	PMID:23603762	PCS		5/11			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0000006	PMID:21076407	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:614563	Cortical dysplasia, complex, with other brain malformations 13		HP:0006821	PMID:23603762	PCS		3/11			P	HPO:probinson[2022-05-30]
OMIM:609254	Senior-Loken syndrome 5		HP:0003774	OMIM:609254	IEA					P	HPO:iea[2009-02-17]
OMIM:609254	Senior-Loken syndrome 5		HP:0000007	PMID:15723066	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609254	Senior-Loken syndrome 5		HP:0000090	OMIM:609254	IEA					P	HPO:iea[2009-02-17]
OMIM:609254	Senior-Loken syndrome 5		HP:0000510	OMIM:609254	IEA					P	HPO:iea[2009-02-17]
OMIM:601608	Spastic paraplegia and Evans syndrome		HP:0000007	OMIM:601608	IEA					I	HPO:iea[2009-02-17]
OMIM:601608	Spastic paraplegia and Evans syndrome		HP:0001258	OMIM:601608	IEA					P	HPO:iea[2009-02-17]
OMIM:601608	Spastic paraplegia and Evans syndrome		HP:0001973	OMIM:601608	IEA					P	HPO:iea[2009-02-17]
OMIM:601608	Spastic paraplegia and Evans syndrome		HP:0004844	OMIM:601608	IEA					P	HPO:iea[2009-02-17]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0001562	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0000089	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0002151	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0002240	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0002490	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0011400	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0002919	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0001639	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0000954	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0000007	PMID:22243966	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0000568	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0000601	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0000218	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0002643	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619053	Mitochondrial complex IV deficiency, nuclear type 10		HP:0001942	PMID:22243966	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002023	PMID:18553553	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001696	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000486	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002024	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0004322	OMIM:243800	PCS					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0005498	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001252	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001092	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001290	OMIM:243800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001409	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000957	PMID:18553553	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000954	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000832	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002617	OMIM:243800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001406	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001249	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001644	OMIM:243800	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0008716	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0031956	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000252	OMIM:243800	PCS					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000054	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001541	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002750	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001382	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0003362	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0030948	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002908	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0034197	PMID:18553553	PCS		1/1			C	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001738	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000407	PMID:18553553	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0007430	OMIM:243800	TAS					P	HPO:probinson[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000007	PMID:16311597	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0004209	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002901	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000444	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000047	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0008846	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0006349	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000126	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000143	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000582	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001597	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001399	PMID:18553553	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000343	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002286	OMIM:243800	PCS					P	HPO:iea[2012-03-01]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001395	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001153	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002240	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0031964	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000819	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001508	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001629	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0007385	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0012050	OMIM:243800	TAS					P	HPO:probinson[2012-08-01]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002714	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0006334	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002557	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002236	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001744	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001545	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000430	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002253	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001362	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0032106	PMID:18553553	PCS		1/1			P	HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0003819	OMIM:243800	PCS					C	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001518	PMID:18553553	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-18]
OMIM:243800	Johanson-Blizzard syndrome		HP:0002209	OMIM:243800	TAS					P	HPO:probinson[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000821	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0008665	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001511	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0001631	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:243800	Johanson-Blizzard syndrome		HP:0000028	OMIM:243800	IEA					P	HPO:iea[2009-02-17]
OMIM:259680	Chronic recurrent multifocal osteomyelitis		HP:0003565	PMID:30532310	PCS		5/6			P	HP:probinson[2019-01-26];HP:probinson[2019-01-26]
OMIM:259680	Chronic recurrent multifocal osteomyelitis		HP:0002653	PMID:30532310	PCS		6/6			P	HP:probinson[2019-01-26]
OMIM:259680	Chronic recurrent multifocal osteomyelitis		HP:0100847	PMID:30532310	PCS					P	HP:probinson[2019-01-26]
OMIM:259680	Chronic recurrent multifocal osteomyelitis		HP:0000007	OMIM:259680	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:259680	Chronic recurrent multifocal osteomyelitis		HP:0001945	PMID:30532310	PCS		2/6			P	HP:probinson[2019-01-26]
OMIM:259680	Chronic recurrent multifocal osteomyelitis		HP:0002754	PMID:30532310	PCS		6/6			P	HP:probinson[2019-01-26]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001298	PMID:18593870	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0002376	PMID:18593870	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0003487	PMID:20528888	PCS		1/3			P	HPO:probinson[2022-03-16];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001250	PMID:20528888;PMID:18593870	PCS		4/8			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0011968	PMID:20528888	PCS		2/3			P	HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001063	PMID:18593870	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001252	PMID:20528888;PMID:18593870	PCS		7/8			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001263	PMID:20528888;PMID:18593870	PCS		6/6			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0003593	PMID:20528888;PMID:18593870	PCS		8/8			C	HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001251	OMIM:602473	IEA					P	HPO:iea[2009-02-17]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0033446	PMID:20528888	PCS		1/1			P	HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0002071	OMIM:602473	IEA					P	HPO:iea[2009-02-17]
OMIM:602473	Encephalopathy, ethylmalonic		HP:6000757	PMID:28933811	PCS					P	HPO:probinson[2024-06-29]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0007183	PMID:20528888	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001508	PMID:20528888	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0008046	OMIM:602473	PCS					P	HPO:probinson[2012-04-06]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0000007	PMID:14732903	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0000967	PMID:20528888;PMID:18593870	PCS		5/8			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0003219	PMID:18593870	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001522	PMID:20528888	PCS		2/3			C	HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0001249	PMID:18593870	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0003688	PMID:20528888;PMID:18593870	PCS		11/11			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0003128	PMID:20528888;PMID:18593870	PCS		6/6			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:602473	Encephalopathy, ethylmalonic		HP:0002028	PMID:20528888;PMID:18593870	PCS		6/8			P	HPO:probinson[2022-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:614211	Deafness, autosomal dominant 33		HP:0003676	PMID:19183916	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:614211	Deafness, autosomal dominant 33		HP:0003621	PMID:19183916	PCS					C	HPO:probinson[2022-10-06]
OMIM:614211	Deafness, autosomal dominant 33		HP:0000407	PMID:19183916	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-10-06]
OMIM:614211	Deafness, autosomal dominant 33		HP:0011462	PMID:19183916	PCS					C	HPO:probinson[2022-10-06]
OMIM:614211	Deafness, autosomal dominant 33		HP:0000360	PMID:19183916	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:614211	Deafness, autosomal dominant 33		HP:0000006	PMID:19183916	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0003621	OMIM:608638	IEA					C	HPO:iea[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000728	OMIM:608638	IEA					P	HPO:iea[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000717	OMIM:608638	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000723	OMIM:608638	TAS					P	HPO:skoehler[2013-06-04]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000733	OMIM:608638	TAS					P	HPO:probinson[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0001426	OMIM:608638	IEA					I	HPO:iea[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000758	OMIM:608638	TAS					P	HPO:probinson[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0003745	OMIM:608638	IEA					I	HPO:iea[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000721	OMIM:608638	IEA					P	HPO:iea[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000732	OMIM:608638	IEA					P	HPO:iea[2009-02-17]
OMIM:608638	Asperger syndrome, susceptibility to, 1		HP:0000753	OMIM:608638	IEA					P	HPO:iea[2009-02-17]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0003493	PMID:28368018	PCS		2/3			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0025289	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0003593	PMID:28368018	PCS		3/3			C	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0025085	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0011896	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0001508	OMIM:617718	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0002719	PMID:28368018	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0002716	OMIM:617718	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0100827	OMIM:617718	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0006532	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0000498	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0002633	OMIM:617718	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0003565	OMIM:617718	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0001287	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0031813	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0002037	PMID:28368018	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0002573	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0200029	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0011227	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0032229	PMID:28368018	PCS		3/3			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0100658	PMID:28368018	PCS		1/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0000007	PMID:28368018	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0000988	PMID:28368018	PCS		3/3			P	HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0001873	PMID:28368018	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617718	Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia		HP:0005537	OMIM:617718	IEA					P	HPO:skoehler[2018-10-08]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0002540	PMID:34489854	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001344	PMID:34489854	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0002650	PMID:34489854	PCS		1/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001772	PMID:34489854	PCS		1/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0003487	PMID:34489854	PCS		2/3			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001266	PMID:34489854	PCS		2/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0002373	PMID:34489854	PCS		1/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001263	PMID:34489854	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0003593	PMID:34489854	PCS		3/4			C	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0002460	PMID:34489854	PCS		3/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001251	PMID:34489854	PCS		0/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0030891	PMID:34489854	PCS		2/2			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0033725	PMID:34489854	PCS		2/2			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0000007	PMID:34489854	PCS					I	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001258	PMID:34489854	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001249	PMID:34489854	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0003623	PMID:34489854	PCS		1/4			C	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001776	PMID:34489854	PCS		1/4			P	HPO:probinson[2022-04-30]
OMIM:619735	Spastic paraplegia 86, autosomal recessive		HP:0001347	PMID:34489854	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:611369	Lethal congenital contracture syndrome 3		HP:0003202	PMID:17701898	PCS					P	HPO:probinson[2013-04-06]
OMIM:611369	Lethal congenital contracture syndrome 3		HP:0002828	OMIM:611369	IEA					P	HPO:skoehler[2019-09-07]
OMIM:611369	Lethal congenital contracture syndrome 3		HP:0000007	PMID:17701898	PCS					I	HPO:probinson[2013-01-09]
OMIM:611369	Lethal congenital contracture syndrome 3		HP:0002804	PMID:17701898	PCS					P	HPO:probinson[2013-04-06]
OMIM:611369	Lethal congenital contracture syndrome 3		HP:0002093	PMID:17701898	PCS					P	HPO:probinson[2013-04-06]
OMIM:611369	Lethal congenital contracture syndrome 3		HP:0003811	PMID:17701898	PCS					C	HPO:probinson[2013-04-06]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0003676	PMID:24562058	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002464	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0004322	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001332	PMID:24562058	PCS		1/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0100291	PMID:24562058	PCS		0/1			P	HPO:probinson[2024-03-08]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002064	OMIM:205100	TAS					P	HPO:probinson[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002460	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001251	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002061	OMIM:205100	TAS					P	HPO:probinson[2015-12-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0000639	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0011463	PMID:24562058	PCS		3/3			C	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0003701	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001324	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0007325	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0003202	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0003444	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001264	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0000252	PMID:24562058	PCS		2/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0003487	PMID:24562058	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0003121	PMID:24562058	PCS		2/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001260	OMIM:205100	TAS					P	HPO:iea[2015-12-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001263	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002193	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0009130	OMIM:205100	IEA					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0007354	PMID:24562058	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0000007	PMID:24562058	PCS					I	HPO:probinson[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002307	OMIM:205100	TAS					P	HPO:skoehler[2010-06-18]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002425	PMID:24562058	PCS		2/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001257	PMID:24562058	PCS		3/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0006986	OMIM:205100	TAS					P	HPO:probinson[2015-12-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002544	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002501	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001276	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002366	OMIM:205100	IEA					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002169	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002167	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0003693	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0000183	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0000020	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0031960	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0033747	PMID:24562058	PCS		0/3			P	HPO:probinson[2024-03-08]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002599	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001347	PMID:24562058	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002179	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002015	OMIM:205100	IEA					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002650	PMID:24562058	PCS		2/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001288	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0001285	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002491	OMIM:205100	TAS					P	HPO:iea[2009-02-17]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0030051	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0008944	PMID:24562058	PCS		1/3			P	HPO:probinson[2022-08-16]
OMIM:205100	Amyotrophic lateral sclerosis 2, juvenile		HP:0002127	OMIM:205100	IEA					P	HPO:iea[2009-02-17]
OMIM:176630	Primary release disorder of platelets		HP:0000132	OMIM:176630	TAS					P	HPO:probinson[2009-02-17]
OMIM:176630	Primary release disorder of platelets		HP:0001892	OMIM:176630	TAS					P	HPO:probinson[2009-02-17]
OMIM:176630	Primary release disorder of platelets		HP:0000978	OMIM:176630	TAS					P	HPO:probinson[2009-02-17]
OMIM:176630	Primary release disorder of platelets		HP:0004406	OMIM:176630	TAS					P	HPO:probinson[2009-02-17]
OMIM:176630	Primary release disorder of platelets		HP:0000006	OMIM:176630	TAS					I	HPO:probinson[2009-02-17]
OMIM:603786	Stargardt disease 4		HP:0012045	OMIM:603786	TAS					P	HPO:skoehler[2013-02-20]
OMIM:603786	Stargardt disease 4		HP:0000608	OMIM:603786	TAS					P	HPO:skoehler[2013-02-20]
OMIM:603786	Stargardt disease 4		HP:0007663	OMIM:603786	TAS					P	HPO:skoehler[2013-02-20]
OMIM:603786	Stargardt disease 4		HP:0000006	OMIM:603786	TAS					I	HPO:skoehler[2013-01-09]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0030799	PMID:23687350;PMID:24515783	PCS		3/4			P	HPO:probinson[2023-01-22];HPO:skoehler[2017-07-13];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000483	OMIM:248000	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0001355	PMID:24515783	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0001256	PMID:23687350;PMID:24515783	PCS		4/4			P	HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000486	PMID:24515783	PCS		1/2			P	HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0003593	PMID:24515783	PCS		2/2			C	HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000280	OMIM:248000	IEA					P	HPO:iea[2009-02-17]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000716	OMIM:248000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0008672	PMID:24515783	PCS		2/2			P	HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000337	PMID:23687350	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000238	PMID:24515783	PCS		0/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2024-03-08]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0002857	PMID:24515783	PCS		1/2			P	HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0008239	OMIM:248000	IEA					P	HPO:iea[2009-02-17]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000256	PMID:23687350;PMID:24515783	PCS		4/4			P	HPO:probinson[2023-01-22];HPO:skoehler[2013-10-22];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0001249	OMIM:248000	IEA					P	HPO:iea[2009-02-17]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000750	OMIM:248000	TAS					P	HPO:skoehler[2014-08-24]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0001263	OMIM:248000	TAS					P	HPO:skoehler[2014-08-24]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0010499	PMID:24515783	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000709	PMID:24515783	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0007074	PMID:23687350	PCS		2/2			P	HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0002608	PMID:24515783	PCS		2/2			P	HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000007	PMID:23687350	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000648	OMIM:248000	IEA					P	HPO:iea[2009-02-17]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000307	PMID:24515783	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000268	PMID:24515783	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-22]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000303	OMIM:248000	TAS					P	HPO:skoehler[2014-08-24]
OMIM:248000	Macrocephaly/megalencephaly syndrome, autosomal recessive		HP:0000545	PMID:24515783	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-22]
OMIM:201400	Acth deficiency, isolated		HP:0001396	OMIM:201400	IEA					P	HPO:skoehler[2019-04-18]
OMIM:201400	Acth deficiency, isolated		HP:0008163	OMIM:201400	IEA					P	HPO:iea[2009-02-17]
OMIM:201400	Acth deficiency, isolated		HP:0011748	OMIM:201400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201400	Acth deficiency, isolated		HP:0001250	OMIM:201400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:201400	Acth deficiency, isolated		HP:0003593	OMIM:201400	IEA					C	HPO:skoehler[2018-10-08]
OMIM:201400	Acth deficiency, isolated		HP:0000007	OMIM:201400	IEA					I	HPO:iea[2009-02-17]
OMIM:201400	Acth deficiency, isolated		HP:0003162	OMIM:201400	IEA					P	HPO:iea[2009-02-17]
OMIM:201400	Acth deficiency, isolated		HP:0000835	OMIM:201400	IEA					P	HPO:iea[2009-02-17]
OMIM:201400	Acth deficiency, isolated		HP:0000952	OMIM:201400	IEA					P	HPO:skoehler[2019-04-18]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0000473	PMID:36543534	PCS		1/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0008804	PMID:36543534	PCS		3/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0004565	PMID:36543534	PCS		4/4			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0004322	PMID:36543534	PCS		2/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0000592	PMID:36543534	PCS	HP:0003577	4/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0003182	PMID:36543534	PCS		5/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0002827	PMID:36543534	PCS		1/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0000938	PMID:36543534	PCS		5/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0002979	PMID:36543534	PCS		5/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0000855	PMID:36543534	PCS		1/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0000007	PMID:36543534	PCS					I	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0002757	PMID:36543534	PCS		2/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0000956	PMID:36543534	PCS		3/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0002857	PMID:36543534	PCS		5/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0001956	PMID:36543534	PCS		5/5			P	HPO:probinson[2024-03-03]
OMIM:620639	Osteogenesis imperfecta, type XXIII		HP:0004349	PMID:36543534	PCS		5/5			P	HPO:probinson[2024-03-03]
OMIM:213010	Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitzsyndrome and meckel syndrome		HP:0100259	OMIM:213010	IEA					P	HPO:iea[2009-02-17]
OMIM:213010	Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitzsyndrome and meckel syndrome		HP:0000079	OMIM:213010	IEA					P	HPO:iea[2009-02-17]
OMIM:213010	Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitzsyndrome and meckel syndrome		HP:0002085	OMIM:213010	IEA					P	HPO:iea[2009-02-17]
OMIM:213010	Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitzsyndrome and meckel syndrome		HP:0001405	OMIM:213010	IEA					P	HPO:iea[2009-02-17]
OMIM:213010	Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitzsyndrome and meckel syndrome		HP:0000007	OMIM:213010	IEA					I	HPO:iea[2009-02-17]
OMIM:213010	Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitzsyndrome and meckel syndrome		HP:0002335	OMIM:213010	IEA					P	HPO:iea[2009-02-17]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0008591	PMID:6476090	PCS					P	HPO:iea[2009-02-17]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0004452	PMID:6476090	PCS					P	HPO:lccarmody[2018-06-29]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0200111	OMIM:128980	TAS					P	HPO:skoehler[2013-06-05]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0011454	PMID:6476090	PCS					P	HPO:lccarmody[2018-06-29]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0008513	PMID:6476090	PCS					P	HPO:lccarmody[2018-06-29]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0000377	PMID:6476090	PCS					P	HPO:lccarmody[2018-06-29]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0000006	PMID:6476090	PCS					I	HPO:iea[2009-02-17]
OMIM:128980	Earlobes, thickened, with conductive deafness from incudostapedialabnormalities		HP:0000347	PMID:6476090	PCS					P	HPO:lccarmody[2018-06-29]
OMIM:615696	Dowling-Degos disease 4		HP:0025114	OMIM:615696	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615696	Dowling-Degos disease 4		HP:0003581	PMID:24387993	PCS					C	HPO:probinson[2023-02-22]
OMIM:615696	Dowling-Degos disease 4		HP:0025092	OMIM:615696	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615696	Dowling-Degos disease 4		HP:0000989	PMID:24387993	PCS					P	HPO:probinson[2023-02-22]
OMIM:615696	Dowling-Degos disease 4		HP:0200034	PMID:24387993	PCS					P	HPO:probinson[2023-02-22]
OMIM:615696	Dowling-Degos disease 4		HP:0000006	PMID:24387993	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-22]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000561	OMIM:305100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002223	PMID:8696334;PMID:8434608	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0010803	OMIM:305100	IEA					P	HPO:iea[2012-03-01]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002046	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002561	OMIM:305100	TAS					P	HPO:skoehler[2012-11-26]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0003196	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0003593	PMID:8696334;PMID:8434608	PCS		2/2			C	HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0045075	OMIM:305100	TAS					P	HPO:probinson[2022-05-08]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0008070	PMID:8434608	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0011830	OMIM:305100	TAS					P	HPO:skoehler[2012-11-26]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000958	PMID:8696334;PMID:8434608	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0012471	PMID:8434608	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0011220	PMID:8696334	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0001609	OMIM:305100	TAS					P	HPO:probinson[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000679	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000977	OMIM:305100	TAS					P	HPO:probinson[2013-08-07]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0001945	PMID:8434608	PCS		1/1			P	HPO:skoehler[2012-11-26];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000653	OMIM:305100	TAS					P	HPO:probinson[2012-03-01]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002557	OMIM:305100	TAS					P	HPO:probinson[2012-06-10]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002019	PMID:8434608	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000336	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0001106	PMID:8696334	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000698	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002213	PMID:8696334	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000970	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000430	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000331	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0007607	OMIM:305100	IEA					P	HPO:skoehler[2015-01-14]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000232	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002299	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002098	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002231	PMID:8434608	PCS		1/1			P	HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000691	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0005280	PMID:8434608	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0001618	OMIM:305100	TAS					P	HPO:skoehler[2012-11-26]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0007592	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0001419	PMID:8434608	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0012384	OMIM:305100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000607	PMID:8696334;PMID:8434608	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000327	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000668	PMID:8696334	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000964	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0007411	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000966	PMID:8434608	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0002007	OMIM:305100	TAS					P	HPO:probinson[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0001598	OMIM:305100	IEA					P	HPO:iea[2009-02-17]
OMIM:305100	Ectodermal dysplasia 1, hypohidrotic, X-linked		HP:0000963	OMIM:305100	TAS					P	HPO:probinson[2013-08-07]
OMIM:132700	Cylindromatosis, familial		HP:0003581	OMIM:132700	IEA					C	HPO:iea[2009-02-17]
OMIM:132700	Cylindromatosis, familial		HP:0008069	OMIM:132700	IEA					P	HPO:skoehler[2009-02-17]
OMIM:132700	Cylindromatosis, familial		HP:0000006	OMIM:132700	IEA					I	HPO:iea[2009-02-17]
OMIM:614588	Dystonia 21		HP:0000473	OMIM:614588	TAS					P	HPO:skoehler[2013-11-28]
OMIM:614588	Dystonia 21		HP:0011462	OMIM:614588	TAS					C	HPO:skoehler[2015-12-30]
OMIM:614588	Dystonia 21		HP:0012049	OMIM:614588	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614588	Dystonia 21		HP:0000006	OMIM:614588	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614588	Dystonia 21		HP:0000643	OMIM:614588	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000176	OMIM:164220	IEA					P	HPO:iea[2009-02-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0011939	OMIM:164220	TAS					P	HPO:probinson[2012-06-10]
OMIM:164220	Schilbach-Rott syndrome		HP:0000286	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000582	OMIM:164220	IEA					P	HPO:iea[2009-02-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000252	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0003189	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0004322	OMIM:164220	TAS		HP:0040283			P	HPO:skoehler[2012-11-28]
OMIM:164220	Schilbach-Rott syndrome		HP:0000193	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000160	OMIM:164220	TAS					P	HPO:skoehler[2012-11-18]
OMIM:164220	Schilbach-Rott syndrome		HP:0000581	OMIM:164220	IEA					P	HPO:iea[2009-02-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0005709	OMIM:164220	TAS					P	HPO:probinson[2012-06-10]
OMIM:164220	Schilbach-Rott syndrome		HP:0008551	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000448	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000601	OMIM:164220	IEA					P	HPO:iea[2009-02-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0030084	OMIM:164220	TAS					P	HPO:skoehler[2014-09-21]
OMIM:164220	Schilbach-Rott syndrome		HP:0000047	OMIM:164220	IEA					P	HPO:iea[2009-02-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0007018	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000006	OMIM:164220	IEA					I	HPO:iea[2009-02-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000358	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164220	Schilbach-Rott syndrome		HP:0000347	OMIM:164220	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0002751	OMIM:612847	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0003301	OMIM:612847	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0009816	OMIM:612847	TAS					P	HPO:probinson[2012-05-27]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0001156	OMIM:612847	TAS				HP:0012825	P	HPO:probinson[2010-06-20]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0004322	OMIM:612847	TAS					P	HPO:probinson[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0002651	OMIM:612847	TAS					P	HPO:skoehler[2015-01-21]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0001061	OMIM:612847	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0012411	OMIM:612847	TAS					P	HPO:skoehler[2015-12-30]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0000869	OMIM:612847	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0000926	OMIM:612847	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0002979	OMIM:612847	TAS					P	HPO:probinson[2010-06-20]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0000007	OMIM:612847	TAS					I	HPO:probinson[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0004626	OMIM:612847	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612847	Brachyolmia 4 with mild epiphyseal and metaphyseal changes		HP:0001007	OMIM:612847	TAS					P	HPO:skoehler[2010-06-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0007737	PMID:20673862	PCS		11/12			P	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0003621	PMID:20673862	PCS		3/6			C	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0000662	PMID:20673862	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0001123	PMID:20673862	PCS		8/8			P	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0000580	PMID:20673862	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0030856	PMID:20673862	PCS		1/12			P	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0100018	PMID:20673862	PCS		1/12			P	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0011463	PMID:20673862	PCS		3/6			C	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0000007	PMID:20673862	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0007663	PMID:20673862	PCS		11/11			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0007787	PMID:20673862	PCS		4/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0000510	PMID:20673862	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0000543	PMID:20673862	PCS		11/12			P	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0007843	PMID:20673862	PCS		11/12			P	HPO:probinson[2021-02-19]
OMIM:613581	Retinitis pigmentosa 56		HP:0007722	PMID:20673862	PCS		10/12			P	HPO:probinson[2021-02-19]
OMIM:608837	Carney complex variant		HP:0000211	PMID:15282353	PCS					P	HPO:probinson[2013-03-09]
OMIM:608837	Carney complex variant		HP:0005684	PMID:15282353	PCS					P	HPO:probinson[2013-01-09]
OMIM:608837	Carney complex variant		HP:0011672	PMID:15282353	PCS					P	HPO:probinson[2013-03-09]
OMIM:608837	Carney complex variant		HP:0000006	PMID:15282353	PCS					I	HPO:probinson[2013-03-09]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0003676	PMID:29395073	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0000750	PMID:29395073	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0001310	PMID:29395073	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0001272	PMID:29395073	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0001252	PMID:29395073	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0002151	PMID:29395073	PCS		0/1			P	HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0001251	PMID:29395073	PCS	HP:0011463	1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0001270	PMID:29395073	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0012675	PMID:29395073	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0011463	PMID:29395073	PCS		1/1			C	HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0000007	PMID:29395073	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0002317	PMID:29395073	PCS	HP:0011463	1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0002505	PMID:29395073	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0000763	PMID:29395073	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0001337	PMID:29395073	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:617917	Neurodegeneration with brain iron accumulation 8		HP:0001347	PMID:29395073	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:608189	Tropical calcific pancreatitis		HP:0002894	OMIM:608189	IEA					P	HPO:iea[2009-02-17]
OMIM:608189	Tropical calcific pancreatitis		HP:0006280	OMIM:608189	TAS					P	HPO:probinson[2009-02-17]
OMIM:608189	Tropical calcific pancreatitis		HP:0005213	OMIM:608189	TAS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2012-09-16]
OMIM:608189	Tropical calcific pancreatitis		HP:0000007	OMIM:608189	IEA					I	HPO:iea[2009-02-17]
OMIM:608189	Tropical calcific pancreatitis		HP:0008205	OMIM:608189	IEA					P	HPO:iea[2009-02-17]
OMIM:608189	Tropical calcific pancreatitis		HP:0000006	OMIM:608189	IEA					I	HPO:iea[2009-02-17]
OMIM:608189	Tropical calcific pancreatitis		HP:0002027	OMIM:608189	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0007902	OMIM:601813	TAS					P	HPO:probinson[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0007917	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0001493	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0003593	OMIM:601813	IEA					C	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0000938	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0000618	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0000007	OMIM:601813	IEA					I	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0007685	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0007663	OMIM:601813	TAS					P	HPO:skoehler[2015-07-26]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0030490	OMIM:601813	TAS					P	HPO:skoehler[2015-08-05]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0001489	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0001147	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0000006	OMIM:601813	IEA					I	HPO:iea[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0007811	OMIM:601813	TAS					P	HPO:probinson[2009-02-17]
OMIM:601813	Exudative vitreoretinopathy 4		HP:0000523	OMIM:601813	IEA					P	HPO:iea[2009-02-17]
OMIM:165670	Ossified ear cartilages		HP:0000598	OMIM:165670	IEA					P	HPO:iea[2009-02-17]
OMIM:165670	Ossified ear cartilages		HP:0000006	OMIM:165670	IEA					I	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0100601	OMIM:189800	TAS					H	HPO:skoehler[2015-01-21]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0000969	OMIM:189800	IEA					P	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0001250	OMIM:189800	IEA					P	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0100602	OMIM:189800	TAS					H	HPO:skoehler[2015-01-21]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0000822	OMIM:189800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0000093	OMIM:189800	IEA					P	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0001511	OMIM:189800	IEA					P	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0001873	OMIM:189800	IEA					P	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0002910	OMIM:189800	IEA					P	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0000006	OMIM:189800	IEA					I	HPO:iea[2009-02-17]
OMIM:189800	Preeclampsia/eclampsia 1		HP:0008071	OMIM:189800	IEA					H	HPO:iea[2009-02-17]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000684	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0004322	PMID:24886874	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000463	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0011937	PMID:24886874	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0003196	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0001252	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0012745	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0011463	PMID:24886874	PCS		1/2			C	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0012471	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0008398	PMID:24886874	PCS		2/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0009882	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000998	PMID:24886874	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0030084	PMID:24886874	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000218	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0009765	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000358	PMID:24886874	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0004712	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0003623	PMID:24886874	PCS		1/2			C	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0002553	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000252	PMID:24886874	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0003189	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000013	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000232	PMID:24886874	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000331	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000430	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000293	PMID:24886874	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000194	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0002033	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0011800	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0005280	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0009891	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000508	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0002209	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000824	PMID:24886874	PCS		0/1			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000527	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000823	PMID:24886874	PCS		1/2			P	HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0001511	PMID:24886874	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0001510	PMID:24886874	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000322	PMID:24886874	PCS		1/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000006	PMID:24886874	PCS					I	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615866	Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism		HP:0000369	PMID:24886874	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-12]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0012265	PMID:24747639	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-09-13]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0003676	PMID:24747639	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0004313	PMID:24747639	PCS		0/8			P	HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0001696	PMID:24747639	PCS		0/15			P	HPO:skoehler[2014-08-03];HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0002110	PMID:24747639	PCS		15/15			P	HPO:skoehler[2014-08-03];HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0011463	PMID:24747639	PCS					C	HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0000789	PMID:24747639	PCS		1/1			P	HPO:skoehler[2014-08-03];HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0033036	PMID:24747639	PCS		6/6			P	HPO:probinson[2020-09-13]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0000007	PMID:24747639	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-13]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0002205	PMID:24747639	PCS		15/15			P	HPO:skoehler[2014-08-03];HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0100750	PMID:24747639	PCS					P	HPO:skoehler[2014-08-03];HPO:probinson[2024-03-15]
OMIM:615872	Ciliary dyskinesia, primary, 29		HP:0012236	PMID:24747639	PCS		0/9			P	HPO:probinson[2024-03-15]
OMIM:273900	Thrombocytopenia 3		HP:0001892	PMID:25876182	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0000132	PMID:25876182	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0003621	PMID:25516138	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0003593	PMID:25876182	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0003010	PMID:25876182	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0012143	PMID:23650215;PMID:25876182	PCS		0/4			P	HPO:probinson[2024-03-09];HPO:probinson[2020-09-06];HPO:probinson[2024-03-09]
OMIM:273900	Thrombocytopenia 3		HP:0011463	PMID:25516138	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0000979	PMID:25876182	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0007420	PMID:25876182	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0000007	PMID:25876182;PMID:25516138	PCS		20/20			I	HPO:iea[2009-02-17];HPO:probinson[2020-09-06];ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0000967	PMID:25516138	PCS	HP:0011463	3/3			P	HPO:probinson[2020-09-06];HPO:probinson[2020-09-06]
OMIM:273900	Thrombocytopenia 3		HP:0000967	PMID:25876182	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0000421	PMID:25516138	PCS	HP:0011463	3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-06]
OMIM:273900	Thrombocytopenia 3		HP:0000421	PMID:25876182	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0001873	PMID:25876182;PMID:25516138	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-06];HPO:probinson[2020-09-06]
OMIM:273900	Thrombocytopenia 3		HP:0005537	PMID:25876182;PMID:25516138	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-06];HPO:probinson[2020-09-06]
OMIM:273900	Thrombocytopenia 3		HP:0005548	PMID:25876182;PMID:25516138	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0001744	PMID:25876182	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:273900	Thrombocytopenia 3		HP:0000225	PMID:25876182	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0010628	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003324	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003676	OMIM:609283	IEA					C	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003200	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0000590	PMID:11756613	PCS	HP:0011462	5/7			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0000590	OMIM:609283	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003581	OMIM:609283	IEA					C	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0000407	OMIM:609283	TAS		4/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0011462	PMID:11756613	PCS		7/7			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0000508	PMID:11756613	PCS	HP:0003596	7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003548	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0000006	OMIM:609283	IEA					I	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003688	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003458	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003546	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:609283	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2		HP:0003689	OMIM:609283	IEA					P	HPO:iea[2009-02-17]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001265	PMID:32693025	PCS		6/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0003477	PMID:32693025	PCS		11/15			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0000252	PMID:32693025	PCS		15/20			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0002059	PMID:32693025	PCS		4/21			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0000365	PMID:32693025	PCS		11/19			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0000750	PMID:32693025	PCS		20/22			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0002650	PMID:32693025	PCS		4/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0002188	PMID:32693025	PCS		3/21			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0004322	PMID:32693025	PCS		18/20			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0003487	PMID:32693025	PCS		1/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001272	PMID:32693025	PCS		2/21			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001252	PMID:32693025	PCS		11/16			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0000580	PMID:32693025	PCS		5/6			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001284	PMID:32693025	PCS		8/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0002194	PMID:32693025	PCS		19/20			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001999	PMID:32693025	PCS		16/20			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0002515	PMID:32693025	PCS		1/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0003701	PMID:32693025	PCS		1/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001257	PMID:32693025	PCS		5/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0000006	PMID:32693025	PCS					I	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001249	PMID:32693025	PCS		18/20			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001347	PMID:32693025	PCS		6/25			P	HPO:probinson[2021-03-08]
OMIM:619090	Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy		HP:0001765	PMID:32693025	PCS		1/25			P	HPO:probinson[2021-03-08]
OMIM:621269	Spermatogenic failure 101		HP:0025133	PMID:33988247	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0030346	PMID:33988247	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0030345	PMID:33988247	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:6000135	PMID:33988247	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0003251	PMID:33988247	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0011462	PMID:33988247	PCS		4/4			C	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0030087	PMID:33988247	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0040171	PMID:33988247	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0000007	PMID:33988247	PCS					I	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621269	Spermatogenic failure 101		HP:0011961	PMID:33988247	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0003763	OMIM:617903	IEA		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0002883	OMIM:617903	IEA		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0030215	PMID:26740508	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0000252	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0001344	PMID:26740508	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0001773	OMIM:617903	IEA		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0006979	PMID:26740508	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0002376	OMIM:617903	IEA		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0001332	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0001288	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0001250	OMIM:617903	IEA		0/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0003593	PMID:26740508	PCS		1/1			C	HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0100023	PMID:26740508	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0007281	PMID:26740508	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0012332	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0000729	PMID:26740508	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0002119	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0000713	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0200055	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0000256	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0002104	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0000006	PMID:26740508	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-06]
OMIM:617903	Neurodevelopmental disorder with poor language and loss of hand skills		HP:0001249	OMIM:617903	IEA					P	HPO:skoehler[2018-10-08]
OMIM:620177	Hypotrichosis 15		HP:0002209	PMID:32336749	PCS		4/4			P	HPO:probinson[2023-03-25]
OMIM:620177	Hypotrichosis 15		HP:0000007	PMID:32336749	PCS					I	HPO:probinson[2023-03-25]
DECIPHER:1	Wolf-Hirschhorn syndrome		HP:0000252	DECIPHER:1	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:1	Wolf-Hirschhorn syndrome		HP:0001250	DECIPHER:1	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:1	Wolf-Hirschhorn syndrome		HP:0001518	DECIPHER:1	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:1	Wolf-Hirschhorn syndrome		HP:0001252	DECIPHER:1	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:1	Wolf-Hirschhorn syndrome		HP:0001249	DECIPHER:1	IEA					P	HPO:skoehler[2013-05-29]
OMIM:603221	Myopia-3		HP:0000541	OMIM:603221	IEA					P	HPO:iea[2009-02-17]
OMIM:603221	Myopia-3		HP:0011003	PMID:9792869	PCS	HP:0003621				P	HPO:iea[2009-02-17];HPO:probinson[2021-04-25]
OMIM:603221	Myopia-3		HP:0000006	PMID:9792869	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-04-25]
OMIM:109543	B-CELL MALIGNANCY, LOW-GRADE		HP:0005550	OMIM:109543	IEA					P	HPO:iea[2009-02-17]
OMIM:109543	B-CELL MALIGNANCY, LOW-GRADE		HP:0000006	OMIM:109543	IEA					I	HPO:iea[2009-02-17]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0002650	PMID:29514872	PCS		5/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0010109	PMID:29514872	PCS		3/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0001156	PMID:29514872	PCS		10/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0001387	PMID:29514872	PCS		2/3			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0003388	PMID:29514872	PCS		2/3			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0001181	PMID:29514872	PCS		4/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0008080	PMID:29514872	PCS		7/10			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0010557	PMID:29514872	PCS		5/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0100259	PMID:29514872	PCS		3/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0002829	PMID:29514872	PCS		2/3			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0010055	PMID:29514872	PCS		3/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0009882	PMID:29514872	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0002938	PMID:29514872	PCS		3/6			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0000767	PMID:29514872	PCS		2/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0001845	PMID:29514872	PCS		6/10			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0000007	PMID:29514872	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0009774	PMID:29514872	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0002999	PMID:29514872	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0001049	PMID:29514872	PCS		4/10			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0001852	PMID:29514872	PCS		4/10			P	HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0009778	PMID:29514872	PCS		4/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:618167	Osteochondrodysplasia, brachydactyly, and overlapping malformed digits		HP:0003502	PMID:29514872	PCS		10/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0002322	PMID:33141179	PCS		6/8			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0003596	PMID:33141179	PCS		4/8			C	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0002067	PMID:33141179	PCS		8/8			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0003431	PMID:33141179	PCS		4/5			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0003584	PMID:33141179	PCS		4/8			C	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0001271	PMID:33141179	PCS		4/5			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0002063	PMID:33141179	PCS		8/8			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0033383	PMID:33141179	PCS		5/5			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0000716	PMID:33141179	PCS		2/5			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0000739	PMID:33141179	PCS		5/5			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0007078	PMID:33141179	PCS		5/5			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0002506	PMID:33141179	PCS		3/5		HP:0012825	P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0002548	PMID:33141179	PCS		8/8			P	HPO:probinson[2021-05-31]
OMIM:619279	Parkinsonism with polyneuropathy		HP:0000006	PMID:33141179	PCS					I	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:621080	Heterotaxy, visceral, 14		HP:0030853	PMID:39753129	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001696	PMID:39753129	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001651	PMID:39753129	PCS		0/13			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0002780	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000085	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0010444	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0010883	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0010882	PMID:39753129	PCS		2/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0011537	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0031349	PMID:39753129	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0011535	PMID:39753129	PCS		3/16			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0012304	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0034188	PMID:39753129	PCS		4/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0011461	PMID:39753129	PCS		3/18			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001643	PMID:39753129	PCS		3/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000278	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000476	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000358	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000494	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0003363	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0033379	PMID:39753129	PCS		2/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0033183	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000767	PMID:39753129	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000007	PMID:39753129	PCS					I	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000961	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000369	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000126	PMID:39753129	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0032092	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0003577	PMID:39753129	PCS		15/18			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000023	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0004383	PMID:39753129	PCS		3/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0005151	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0031565	PMID:39753129	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001629	PMID:39753129	PCS		4/16			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0011682	PMID:39753129	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0011560	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001746	PMID:39753129	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001669	PMID:39753129	PCS		2/16			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0006772	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0006695	PMID:39753129	PCS		3/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001748	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0030084	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001747	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0004935	PMID:39753129	PCS		0/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000218	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000034	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0002099	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0031298	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0010772	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0011861	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0005280	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0031854	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0011671	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001719	PMID:39753129	PCS		5/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000822	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0002205	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0001631	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0002566	PMID:39753129	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621080	Heterotaxy, visceral, 14		HP:0000347	PMID:39753129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0002553	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000494	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000233	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0001250	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0001263	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0001290	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0005280	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000708	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0008770	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000319	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000739	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000316	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000007	OMIM:617532	TAS					I	HPO:nvasilevsky[2018-07-25]
OMIM:617532	Intellectual developmental disorder with neuropsychiatric features		HP:0000325	OMIM:617532	TAS					P	HPO:nvasilevsky[2018-07-25]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000286	PMID:20882035	PCS		5/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000483	PMID:19684605	PCS		3/25			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000486	PMID:23918763;PMID:19684605	PCS		15/30			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0004322	PMID:20882035	PCS		8/8			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001290	PMID:23918763	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0004482	PMID:20882035	PCS		8/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000081	PMID:23918763	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0011974	PMID:23918763	PCS		1/5			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0006191	OMIM:607721	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000957	PMID:20882035	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0011220	PMID:19684605;PMID:20882035	PCS		26/29			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001609	PMID:19684605	PCS		6/25			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001928	PMID:19684605;PMID:20882035	PCS		9/31			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000316	PMID:19684605;PMID:20882035	PCS		26/33			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000953	PMID:23918763;PMID:19684605	PCS		13/29			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000752	PMID:19684605;PMID:20882035	PCS		14/32			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001642	PMID:23918763;PMID:19684605;PMID:20882035	PCS		15/37			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001249	PMID:19684605;PMID:20882035	PCS		27/32			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000358	PMID:19684605	PCS		22/25			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000494	PMID:20882035	PCS		4/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0002079	OMIM:607721	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0011968	PMID:23918763	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001382	PMID:23918763	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001263	PMID:23918763	PCS		5/5			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000964	PMID:23918763;PMID:19684605;PMID:20882035	PCS		18/37			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000766	PMID:19684605;PMID:20882035	PCS		17/32			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000527	PMID:23918763	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001659	PMID:23918763	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000006	PMID:19684605	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000369	PMID:19684605;PMID:20882035	PCS		30/33			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001611	PMID:19684605;PMID:20882035	PCS		10/31			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000962	PMID:20882035	PCS		5/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000341	PMID:19684605	PCS		2/25			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000540	PMID:19684605	PCS		4/25			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000023	PMID:23918763	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0008070	PMID:20882035	PCS		8/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001629	PMID:19684605;PMID:20882035	PCS		3/33			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001508	PMID:20882035	PCS		8/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000337	PMID:20882035	PCS		7/7			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000218	PMID:20882035	PCS		6/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000256	PMID:23918763;PMID:19684605	PCS		27/30			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000974	PMID:20882035	PCS		5/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001028	PMID:23918763	PCS		2/5			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0002212	PMID:20882035	PCS		6/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001561	PMID:23918763	PCS	HP:0011461	3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001561	PMID:20882035	PCS		1/7			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001520	PMID:23918763	PCS		3/5			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001003	PMID:20882035	PCS		2/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0031936	PMID:20882035	PCS		7/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000470	PMID:23918763;PMID:19684605;PMID:20882035	PCS		25/38			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0040169	PMID:23918763;PMID:19684605	PCS		22/22			P	HPO:probinson[2021-05-20];HPO:skoehler[2015-08-02];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0008064	PMID:19684605	PCS		2/25			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0032152	PMID:19684605	PCS		8/25			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001639	PMID:23918763;PMID:19684605;PMID:20882035	PCS		10/37			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000508	PMID:19684605;PMID:20882035	PCS		24/33			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0002209	PMID:19684605	PCS		25/25			P	HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0002967	PMID:20882035	PCS		2/8			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0001631	PMID:23918763;PMID:19684605;PMID:20882035	PCS		12/36			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000465	PMID:23918763;PMID:19684605;PMID:20882035	PCS		22/38			P	HPO:probinson[2021-05-20];HPO:skoehler[2013-05-03];HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0007018	PMID:23918763	PCS		1/1			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000545	PMID:19684605	PCS		3/25			P	HPO:probinson[2021-05-20]
OMIM:607721	Noonan syndrome-like with loose anagen hair 1		HP:0000028	PMID:20882035	PCS		2/4			P	HPO:probinson[2021-05-20]
OMIM:102370	Acromicric dysplasia		HP:0003510	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0003026	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0004279	OMIM:102370	TAS					P	HPO:probinson[2009-02-17]
OMIM:102370	Acromicric dysplasia		HP:0000343	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0001773	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0002002	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0000463	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0002750	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0003300	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0000160	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0010049	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0001072	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0010579	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0001609	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0000414	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0000527	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0000311	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0000179	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:102370	Acromicric dysplasia		HP:0000006	OMIM:102370	TAS					I	HPO:probinson[2009-02-17]
OMIM:102370	Acromicric dysplasia		HP:0005900	OMIM:102370	TAS					P	HPO:probinson[2009-02-17]
OMIM:102370	Acromicric dysplasia		HP:0009803	OMIM:102370	TAS					P	HPO:probinson[2012-06-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001276	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002301	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001250	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0003573	PMID:15356310	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001252	OMIM:603553	TAS					P	HPO:skoehler[2014-11-26]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0003075	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002383	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0003593	PMID:18710388;PMID:14757862	PCS		23/23			C	HPO:probinson[2020-10-31];HPO:probinson[2020-10-31];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002240	PMID:18710388;PMID:15356310	PCS		14/14			P	HPO:probinson[2020-10-31];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001251	PMID:21234777	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0003073	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001290	OMIM:603553	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0012229	PMID:17873118;PMID:21234777	PCS		25/49			P	HPO:probinson[2020-10-03];HPO:probinson[2013-04-07];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0012177	PMID:11179007;PMID:14757862	PCS		26/26			P	HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0012156	PMID:11179007;PMID:18710388;PMID:17873118	PCS		85/97			P	HPO:probinson[2013-01-07];HPO:probinson[2020-10-03];HPO:probinson[2020-10-31];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0008151	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001508	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0000737	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001903	PMID:17873118;PMID:21234777	PCS		79/85			P	HPO:probinson[2020-10-03];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002716	PMID:12229880;PMID:18710388;PMID:17873118	PCS		36/98			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-03];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001945	PMID:11179007;PMID:18710388;PMID:17873118	PCS		102/105			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002516	PMID:21234777	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002910	PMID:11179007;PMID:12229880	PCS		3/3			P	HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0000952	OMIM:603553;PMID:18710388	PCS		19/21			P	HPO:probinson[2020-10-31];HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001744	PMID:11179007;PMID:18710388;PMID:17873118	PCS		109/111			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-03];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0007305	PMID:12229880	PCS		1/1			P	HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001287	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002155	PMID:11179007;PMID:12229880;PMID:18710388;PMID:17873118	PCS		81/103			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-03];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001882	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001263	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0011900	PMID:11179007;PMID:12229880;PMID:18710388;PMID:17873118	PCS		86/102			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-03];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0003281	PMID:12229880;PMID:18710388;PMID:17873118;PMID:21234777	PCS		65/71			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-03];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0000969	PMID:18710388	PCS		3/9			P	HPO:probinson[2020-10-31]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0007430	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002902	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0000007	PMID:10583959	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001954	PMID:12229880	IEA		2/2			P	HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002922	PMID:21234777	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0000988	PMID:18710388;PMID:17873118	PCS		22/84			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001433	PMID:12229880	PCS		2/2			P	HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001873	PMID:17873118	PCS		88/88			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0002445	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001876	PMID:12229880	PCS		2/2			P	HPO:probinson[2020-10-03]
OMIM:603553	Hemophagocytic lymphohistiocytosis, familial, 2		HP:0001259	OMIM:603553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231070	Geroderma osteodysplasticum		HP:0002982	OMIM:231070	TAS					P	HPO:skoehler[2015-02-22]
OMIM:231070	Geroderma osteodysplasticum		HP:0003510	OMIM:231070	IEA					P	HPO:iea[2009-02-17]
OMIM:231070	Geroderma osteodysplasticum		HP:0001595	PMID:18348262	PCS		0/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2024-03-08]
OMIM:231070	Geroderma osteodysplasticum		HP:0000164	PMID:18348262	PCS		0/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2024-03-08]
OMIM:231070	Geroderma osteodysplasticum		HP:0003577	PMID:18348262	PCS		8/8			C	HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0002980	PMID:18348262	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0004586	OMIM:231070	IEA					P	HPO:iea[2009-02-17]
OMIM:231070	Geroderma osteodysplasticum		HP:0002783	PMID:18348262	PCS		4/8			P	HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000939	OMIM:231070	IEA					P	HPO:iea[2009-02-17]
OMIM:231070	Geroderma osteodysplasticum		HP:0000938	PMID:18348262	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000316	PMID:18348262	PCS		0/8			P	HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0002757	PMID:18348262	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0002659	PMID:18348262	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0002953	OMIM:231070	IEA					P	HPO:iea[2009-02-17]
OMIM:231070	Geroderma osteodysplasticum		HP:0005328	PMID:18348262	PCS					P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0001249	PMID:18348262	PCS		7/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000973	PMID:18348262	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0002751	OMIM:231070	IEA					P	HPO:skoehler[2018-10-08]
OMIM:231070	Geroderma osteodysplasticum		HP:0003301	OMIM:231070	TAS					P	HPO:skoehler[2015-12-30]
OMIM:231070	Geroderma osteodysplasticum		HP:0000252	PMID:18348262	PCS		3/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0001187	PMID:18348262	PCS		8/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000494	PMID:18348262	PCS		0/8			P	HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000750	PMID:18348262	PCS		4/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000490	PMID:18348262	PCS		3/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000272	OMIM:231070	IEA					P	HPO:iea[2009-02-17]
OMIM:231070	Geroderma osteodysplasticum		HP:0003160	PMID:18348262	PCS		0/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2024-03-08]
OMIM:231070	Geroderma osteodysplasticum		HP:0012385	PMID:18348262	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0100678	PMID:18348262	PCS	HP:0003577	8/8			P	HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000704	PMID:18348262	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000926	OMIM:231070	TAS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000327	PMID:18348262	PCS		8/8			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000007	PMID:18997784	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:231070	Geroderma osteodysplasticum		HP:0002645	PMID:18348262	PCS		0/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0007414	PMID:18348262	PCS		8/8			P	HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0000303	PMID:18348262	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:231070	Geroderma osteodysplasticum		HP:0004568	OMIM:231070	IEA					P	HPO:iea[2009-02-17]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000343	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0008905	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000486	OMIM:616638	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001355	PMID:25851998	PCS		1/4			P	HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0005257	PMID:25851998	PCS	HP:0003593	4/4			P	HPO:skoehler[2019-04-18]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001250	PMID:25851998	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000260	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0003196	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0003593	PMID:25851998	PCS		3/3			C	HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001290	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0006191	PMID:25851998	PCS		3/3			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0012650	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000957	PMID:25851998	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000319	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0009882	OMIM:616638	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000316	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001943	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001869	PMID:25851998	PCS		3/3			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000219	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0002119	PMID:25851998	PCS		3/3			P	HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000256	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0007206	OMIM:616638	TAS					P	HPO:lccarmody[2018-10-25];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001249	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0002212	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001540	PMID:25851998	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000154	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000494	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001520	OMIM:616638	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000331	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0002079	PMID:25851998	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0011968	OMIM:616638	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000194	PMID:25851998	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0011800	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0005280	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0034295	PMID:25851998	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0010241	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001537	PMID:25851998	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000348	PMID:25851998	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0002007	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0001873	OMIM:616638	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000006	PMID:25851998	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-08]
OMIM:616638	Smith-Kingsmore syndrome		HP:0000028	OMIM:616638	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616638	Smith-Kingsmore syndrome		HP:0002720	PMID:25851998;OMIM:616638	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-08]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0003236	PMID:37907725	PCS		4/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0003596	PMID:37907725	PCS		7/7			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0003394	PMID:37907725	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0002380	PMID:37907725	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0100295	PMID:37907725	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0033685	PMID:37907725	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0033747	PMID:37907725	PCS		0/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0040132	PMID:37907725	PCS		0/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0034045	PMID:37907725	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0009027	PMID:37907725	PCS		6/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0003805	PMID:37907725	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0011808	PMID:37907725	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0003445	PMID:37907725	PCS		6/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0008959	PMID:37907725	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0009072	PMID:37907725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0033383	PMID:37907725	PCS		5/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0009053	PMID:37907725	PCS		7/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0001712	PMID:37907725	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0002505	PMID:37907725	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0003438	PMID:37907725	PCS		6/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0000006	PMID:37907725	PCS					I	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0008944	PMID:37907725	PCS		7/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621094	Neuronopathy, distal hereditary motor, autosomal dominant 15		HP:0006844	PMID:37907725	PCS		2/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0004268	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0004322	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0008473	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0008464	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0002812	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0002944	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0008423	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0008467	OMIM:601344	IEA					P	HPO:iea[2009-02-17]
OMIM:601344	Spinal dysplasia, Anhalt type		HP:0000006	OMIM:601344	IEA					I	HPO:iea[2009-02-17]
OMIM:617526	Erythrokeratodermia variabilis et progressiva 4		HP:0003577	PMID:28575652	PCS		4/4			C	HPO:probinson[2022-03-28]
OMIM:617526	Erythrokeratodermia variabilis et progressiva 4		HP:0025092	PMID:28575652	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617526	Erythrokeratodermia variabilis et progressiva 4		HP:0000007	PMID:28575652	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617526	Erythrokeratodermia variabilis et progressiva 4		HP:0010783	PMID:28575652	PCS	HP:0003623	4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-28]
OMIM:617526	Erythrokeratodermia variabilis et progressiva 4		HP:0000972	PMID:28575652	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-28]
OMIM:617526	Erythrokeratodermia variabilis et progressiva 4		HP:0007479	PMID:28575652	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617526	Erythrokeratodermia variabilis et progressiva 4		HP:0000962	PMID:28575652	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-28]
OMIM:618173	Retinitis pigmentosa 83		HP:0001133	PMID:30932721;PMID:26964041	PCS		4/5			P	HPO:probinson[2021-02-14];HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0100832	PMID:26964041	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0007737	PMID:30932721;PMID:26964041	PCS		12/12			P	HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0003621	PMID:30932721	PCS		2/2			C	HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0000662	PMID:30932721;PMID:26964041	PCS		12/12			P	HPO:probinson[2021-02-14];HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0030672	PMID:30932721	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0007663	PMID:30932721;PMID:26964041	PCS		5/5			P	HPO:probinson[2021-02-14];HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0011505	PMID:26964041	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0000510	PMID:26964041	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0007787	PMID:26964041	PCS		3/3			P	HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0007843	PMID:26964041	PCS					P	HPO:probinson[2021-02-14]
OMIM:618173	Retinitis pigmentosa 83		HP:0000006	PMID:26964041	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-14]
OMIM:611631	Epilepsy, familial temporal lobe, 4		HP:0002384	OMIM:611631	TAS					P	HPO:skoehler[2012-09-20]
OMIM:611631	Epilepsy, familial temporal lobe, 4		HP:0002077	OMIM:611631	TAS					P	HPO:skoehler[2009-02-17]
OMIM:611631	Epilepsy, familial temporal lobe, 4		HP:0011165	OMIM:611631	TAS					P	HPO:skoehler[2012-09-20]
OMIM:611631	Epilepsy, familial temporal lobe, 4		HP:0003829	OMIM:611631	TAS					I	HPO:skoehler[2009-02-17]
OMIM:611631	Epilepsy, familial temporal lobe, 4		HP:0008765	OMIM:611631	TAS					P	HPO:skoehler[2010-06-20]
OMIM:611631	Epilepsy, familial temporal lobe, 4		HP:0002349	OMIM:611631	TAS					P	HPO:probinson[2012-09-20]
OMIM:611631	Epilepsy, familial temporal lobe, 4		HP:0000006	OMIM:611631	TAS					I	HPO:skoehler[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001397	PMID:34177791	PCS		1/1			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0003577	PMID:29098565	PCS		6/6			C	HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0006528	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0005598	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0002860	PMID:29098565	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:210900	Bloom syndrome		HP:0001010	PMID:34177791	PCS		1/1			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0025300	PMID:29098565	PCS		5/5			P	HPO:probinson[2021-06-25]
OMIM:210900	Bloom syndrome		HP:0003593	PMID:34177791	PCS		1/1			C	HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0005590	PMID:34177791	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0001909	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000957	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0040012	OMIM:210900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210900	Bloom syndrome		HP:0000998	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001328	OMIM:210900	TAS					P	HPO:probinson[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0008897	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0040217	PMID:34177791	PCS		1/1			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0000411	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001620	OMIM:210900	TAS					P	HPO:probinson[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0004315	OMIM:210900	TAS					P	HPO:probinson[2012-07-16]
OMIM:210900	Bloom syndrome		HP:0002850	OMIM:210900	TAS					P	HPO:probinson[2012-07-16]
OMIM:210900	Bloom syndrome		HP:0000275	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000252	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000992	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0003220	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001041	PMID:34177791	PCS		1/1			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0002110	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001161	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000690	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000272	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001518	PMID:29098565	PCS	HP:0003577	6/6			P	HPO:probinson[2021-06-25]
OMIM:210900	Bloom syndrome		HP:0000448	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000007	OMIM:210900	IEA					I	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000868	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0004209	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000268	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001511	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0002788	PMID:29098565;PMID:34177791	PCS		7/7			P	HPO:probinson[2021-06-25];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0001159	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0001510	PMID:34177791	PCS		1/1			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0005978	PMID:34177791	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:210900	Bloom syndrome		HP:0000028	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0002720	OMIM:210900	TAS					P	HPO:probinson[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0002665	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:210900	Bloom syndrome		HP:0000027	OMIM:210900	IEA					P	HPO:iea[2009-02-17]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0002025	PMID:22683086	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000582	OMIM:614749	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0010804	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0003577	PMID:22683086	PCS		3/3			C	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000365	OMIM:614749	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0002023	PMID:22683086	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001250	PMID:22683086	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0003155	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0003196	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001252	PMID:22683086	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0011316	PMID:22683086	PCS		1/3			P	HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001804	PMID:22683086	PCS		3/3			P	HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0010055	PMID:22683086	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000316	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0002119	PMID:22683086	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000637	PMID:22683086	PCS		3/3			P	HPO:skoehler[2013-05-29];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000455	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001249	PMID:22683086	PCS		3/3			P	HPO:skoehler[2015-01-19];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0006118	PMID:22683086	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000076	PMID:22683086	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000252	PMID:22683086	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000175	OMIM:614749	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000431	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000750	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0031936	PMID:22683086	PCS		3/3			P	HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001263	PMID:22683086	PCS		3/3			P	HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0002251	PMID:22683086	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0011326	PMID:22683086	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0000007	PMID:22683086	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0004969	PMID:22683086	PCS		1/3			P	HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001357	PMID:22683086	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001510	PMID:22683086	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-08]
OMIM:614749	Hyperphosphatasia with impaired intellectual development syndrome 2		HP:0001631	PMID:22683086	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-08]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000483	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0004322	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0003196	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0012745	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0045075	PMID:19126570	PCS		3/3			P	HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000958	OMIM:613026	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0011461	PMID:19126570	PCS		3/3			C	HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001845	PMID:19126570	PCS		1/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0008897	OMIM:613026	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000637	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0003745	OMIM:613026	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000278	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001249	PMID:19126570	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0006315	PMID:19126570	PCS		1/3			P	HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000252	PMID:19126570	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001263	PMID:19126570	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0010554	PMID:19126570	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0003758	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0004209	PMID:19126570	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000400	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000048	PMID:19126570	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000322	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000047	PMID:19126570	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000369	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000006	OMIM:613026	TAS					I	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001671	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000023	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000463	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001195	PMID:19126570	PCS		1/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0002164	PMID:19126570	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000581	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0008070	PMID:19126570	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0002719	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001508	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0007385	PMID:19126570	PCS		3/3			P	HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0008872	PMID:19126570	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0006610	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000653	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000670	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000431	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000233	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000430	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000276	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0002373	OMIM:613026	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000508	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000668	OMIM:613026	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000348	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001511	PMID:19126570	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0001510	PMID:19126570	PCS		3/3			P	HPO:probinson[2021-07-06]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000347	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613026	Chromosome 19q13.11 deletion syndrome, distal		HP:0000028	OMIM:613026	IEA					P	HPO:skoehler[2010-06-19]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0003510	PMID:34470639	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0004474	PMID:34470639	PCS		1/1			P	HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0030353	PMID:34470639	PCS		1/1			P	HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0003593	PMID:34470639	PCS		1/1			C	HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0000007	OMIM:262400	IEA					I	HPO:iea[2009-02-17]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0000348	PMID:34470639	PCS		1/1			P	HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0001943	PMID:34470639	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0034323	PMID:34470639	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0001510	PMID:34470639	PCS		1/1			P	HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0000457	PMID:34470639	PCS		1/1			P	HPO:probinson[2022-07-03]
OMIM:262400	Growth hormone deficiency, isolated, type IA		HP:0006579	PMID:34470639	PCS		1/1			P	HPO:probinson[2022-07-03]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001298	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000286	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000486	PMID:27389779	PCS		3/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000463	PMID:27389779	PCS					P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001332	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001250	PMID:27389779	PCS	HP:0003593	6/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001252	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001290	PMID:27389779	PCS		7/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0045075	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000639	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0100704	PMID:27389779	PCS		3/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000938	PMID:27389779	PCS		3/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0011220	PMID:27389779	PCS					P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000414	PMID:27389779	PCS					P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0002119	PMID:27334371	PCS		1/1			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000256	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000179	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001249	PMID:27389779	PCS		4/4			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000154	PMID:27389779	PCS					P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0002059	PMID:27334371	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001344	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0002353	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000574	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0031936	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0002197	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000490	PMID:27389779	PCS		3/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0001263	PMID:27389779	PCS		7/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0011800	PMID:27389779	PCS					P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0005280	PMID:27389779	PCS					P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0100660	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0100023	PMID:27389779	PCS		4/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000506	OMIM:617268	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000729	PMID:27389779	PCS		2/3			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0040288	PMID:27389779	PCS		4/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000508	PMID:27389779	PCS		2/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0002705	PMID:27389779	PCS					P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0100716	PMID:27389779	PCS		2/7			P	HP:probinson[2018-07-05]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000400	OMIM:617268	TAS					P	HP:probinson[2018-07-05];HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0002500	PMID:27334371	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:617268	Neurodevelopmental disorder with hypotonia, seizures, and absent language		HP:0000006	PMID:27389779	PCS					I	HP:probinson[2018-07-05]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0002961	PMID:20499091	PCS					P	HPO:skoehler[2013-01-11];HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0410242	PMID:15100680	PCS					P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0003496	PMID:15100680;PMID:20499091	PCS		3/8			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0003261	PMID:15100680	IEA		5/6			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0040042	PMID:20499091	PCS		1/1			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0008070	PMID:20499091	PCS		1/1			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0012177	PMID:15100680	PCS		7/7			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0032163	PMID:15100680;PMID:20499091	PCS		3/8			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0000968	PMID:20499091	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0001419	PMID:27368913	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0031692	PMID:15100680	PCS		1/7			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0011065	PMID:20499091	IEA		1/1			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0002718	PMID:20499091	PCS		1/1			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0002718	PMID:15100680	PCS	HP:0003593	7/7			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0002007	PMID:20499091	PCS		1/1			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0001004	PMID:20499091	PCS		1/1			P	HPO:probinson[2020-08-12]
OMIM:300291	Ectodermal dysplasia and immunodeficiency 1		HP:0002721	PMID:20499091	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2020-08-12]
OMIM:215850	Cleft-Limb-Heart malformation syndrome		HP:0001660	OMIM:215850	IEA					P	HPO:iea[2009-02-17]
OMIM:215850	Cleft-Limb-Heart malformation syndrome		HP:0001507	OMIM:215850	IEA					P	HPO:iea[2009-02-17]
OMIM:215850	Cleft-Limb-Heart malformation syndrome		HP:0000007	OMIM:215850	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:215850	Cleft-Limb-Heart malformation syndrome		HP:0001159	OMIM:215850	IEA					P	HPO:skoehler[2010-06-20]
OMIM:619245	Premature ovarian failure 19		HP:0008209	PMID:32845237	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:619245	Premature ovarian failure 19		HP:0000869	PMID:32845237	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:619245	Premature ovarian failure 19		HP:0000858	PMID:32845237	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:619245	Premature ovarian failure 19		HP:0008222	PMID:32845237	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:619245	Premature ovarian failure 19		HP:0000007	PMID:32845237	PCS					I	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0001892	PMID:25061177	PCS		2/2			P	HPO:skoehler[2015-02-22]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0000132	PMID:25061177	PCS		1/1	FEMALE		P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-02]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0001903	PMID:25061177	PCS		1/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-04-02]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0003593	PMID:25061177	PCS		2/2			C	HPO:probinson[2023-04-02]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0007420	PMID:25061177	PCS		1/2			P	HPO:skoehler[2015-02-22]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0000007	PMID:25061177	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-02]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0040185	PMID:25061177	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-02]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0000421	PMID:25061177	PCS		2/2			P	HPO:skoehler[2015-02-22]
OMIM:616176	Bleeding disorder, platelet-type, 19		HP:0001873	PMID:25061177	PCS		2/2			P	HPO:probinson[2023-04-02]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0002069	PMID:15502825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0001034	OMIM:609056	TAS					P	HPO:skoehler[2015-12-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0000365	OMIM:609056	TAS		HP:0040283			P	HPO:skoehler[2013-06-04]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0002283	PMID:15502825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0001252	PMID:15502825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0003593	PMID:15502825	PCS					C	HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0010841	PMID:15502825	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0001508	PMID:15502825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0100704	PMID:15502825	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0000737	PMID:15502825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0008872	PMID:15502825	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0012391	PMID:15502825	PCS		8/8			P	HPO:probinson[2013-12-19];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0003623	PMID:15502825	PCS					C	HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0006834	PMID:15502825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0000572	OMIM:609056	IEA					P	HPO:iea[2009-02-17]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0000252	OMIM:609056	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0001344	OMIM:609056	IEA					P	HPO:iea[2009-02-17]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0002133	OMIM:609056	TAS					P	HPO:skoehler[2013-06-04]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0001266	PMID:15502825	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0002376	PMID:15502825	PCS		8/8			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0002013	PMID:15502825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0002395	PMID:15502825	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0001263	PMID:15502825	PCS		8/8			P	HPO:skoehler[2013-06-04];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0000007	PMID:15502825	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-30]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0000648	OMIM:609056	IEA					P	HPO:iea[2009-02-17]
OMIM:609056	Salt and pepper developmental regression syndrome		HP:0001336	OMIM:609056	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612310	Premature ovarian failure 6		HP:0008209	PMID:18499083	PCS					P	HPO:probinson[2013-01-09]
OMIM:612310	Premature ovarian failure 6		HP:0000013	PMID:18499083	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-06-20]
OMIM:612310	Premature ovarian failure 6		HP:0001470	PMID:18499083	PCS					I	HPO:probinson[2013-04-06]
OMIM:612310	Premature ovarian failure 6		HP:0000869	PMID:18499083	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2020-06-20]
OMIM:612310	Premature ovarian failure 6		HP:0011969	PMID:30474133	PCS					P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:612310	Premature ovarian failure 6		HP:0008222	PMID:18499083	IEA		4/4			P	HPO:probinson[2020-11-29]
OMIM:612310	Premature ovarian failure 6		HP:0008232	PMID:30474133	PCS					P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:612310	Premature ovarian failure 6		HP:0010464	PMID:18499083	PCS		2/4			P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:612310	Premature ovarian failure 6		HP:0000786	PMID:30474133	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2020-06-20]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0002069	PMID:16491085	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0000750	PMID:16491085	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0002133	PMID:16491085	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0000486	PMID:16491085	PCS		1/2			P	HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0002123	PMID:16491085	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:6000268	PMID:16491085	PCS		2/2			P	HPO:probinson[2024-02-09]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0001263	PMID:16491085	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0001252	PMID:16491085	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0010851	PMID:16491085	PCS		4/5			P	HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0034365	PMID:16491085	PCS					P	HPO:probinson[2022-09-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0000007	PMID:16491085	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0000238	PMID:16491085	PCS		2/5			P	HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0020221	PMID:16491085	PCS		6/6			P	HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0025116	OMIM:266100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0001249	PMID:16491085	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0002643	PMID:16491085	PCS	HP:0003623	4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0001557	PMID:16491085	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-05]
OMIM:266100	Epilepsy, pyridoxine-dependent		HP:0003623	PMID:16491085	PCS		7/7			C	HPO:probinson[2022-06-05];HPO:probinson[2022-06-05]
OMIM:619523	Anemia, sideroblastic, 5		HP:0003621	PMID:32634119	PCS		1/1			C	HPO:probinson[2021-10-23]
OMIM:619523	Anemia, sideroblastic, 5		HP:0004840	PMID:32634119	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619523	Anemia, sideroblastic, 5		HP:0001903	PMID:32634119	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619523	Anemia, sideroblastic, 5		HP:0004828	PMID:32634119	PCS		1/1			P	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619523	Anemia, sideroblastic, 5		HP:0000007	PMID:32634119	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619523	Anemia, sideroblastic, 5		HP:0031851	PMID:32634119	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619523	Anemia, sideroblastic, 5		HP:0001873	PMID:32634119	PCS		1/1			P	HPO:probinson[2021-10-23]
OMIM:619523	Anemia, sideroblastic, 5		HP:0001875	PMID:32634119	PCS		1/1		HP:0012825	P	HPO:probinson[2021-10-23]
OMIM:600072	Fatal familial insomnia		HP:0002015	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0000651	OMIM:600072	TAS					P	HPO:skoehler[2013-01-22]
OMIM:600072	Fatal familial insomnia		HP:0001260	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0003581	PMID:1439789	PCS		15/15			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:600072	Fatal familial insomnia		HP:0001251	PMID:1439789	PCS		13/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:600072	Fatal familial insomnia		HP:0012332	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0100785	PMID:1439789	PCS		13/15			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-22]
OMIM:600072	Fatal familial insomnia		HP:0000726	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0006790	PMID:1439789	PCS		3/13			P	HPO:probinson[2023-02-22]
OMIM:600072	Fatal familial insomnia		HP:0000975	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0002529	OMIM:600072	TAS					P	HPO:skoehler[2013-01-22]
OMIM:600072	Fatal familial insomnia		HP:0001945	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0001824	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0002019	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0002104	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0000006	OMIM:600072	IEA					I	HPO:iea[2009-02-17]
OMIM:600072	Fatal familial insomnia		HP:0001336	PMID:1439789	PCS		15/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:600072	Fatal familial insomnia		HP:0000016	OMIM:600072	IEA					P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001265	OMIM:118300	IEA					P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003621	PMID:12578939	PCS		1/1			C	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003431	PMID:12578939	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003376	OMIM:118300	IEA					P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001288	PMID:12578939	PCS		1/1			P	HPO:probinson[2023-04-09]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001761	OMIM:118300	IEA					P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003693	PMID:12578939	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001284	OMIM:118300	IEA					P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0002460	PMID:12578939	PCS		1/1			P	HPO:skoehler[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003690	PMID:12578939	PCS		1/1			P	HPO:skoehler[2012-11-16]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003393	PMID:12578939	PCS		1/1			P	HPO:probinson[2023-04-09]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001171	OMIM:118300	IEA					P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0011463	OMIM:118300	TAS					C	HPO:skoehler[2012-10-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0000407	PMID:12578939	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0031374	PMID:12578939	PCS		1/1			P	HPO:probinson[2023-04-09]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0009027	PMID:12578939	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0002936	PMID:12578939	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001884	OMIM:118300	IEA					P	HPO:iea[2009-02-17]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003427	PMID:12578939	PCS		1/1			P	HPO:probinson[2023-04-09]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0000006	PMID:10330345	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001337	PMID:12578939	PCS		1/1			P	HPO:probinson[2023-04-09]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0003447	PMID:12578939	PCS		1/1			P	HPO:probinson[2023-04-09]
OMIM:118300	Charcot-Marie-Tooth disease and deafness		HP:0001765	OMIM:118300	IEA					P	HPO:iea[2009-02-17]
OMIM:616604	Chromosome 14q32 duplication syndrome, 700-kb		HP:0003581	PMID:26280900	PCS					C	HPO:probinson[2023-02-10]
OMIM:616604	Chromosome 14q32 duplication syndrome, 700-kb		HP:0004808	PMID:26280900	PCS					P	HPO:probinson[2023-02-10]
OMIM:616604	Chromosome 14q32 duplication syndrome, 700-kb		HP:0003829	PMID:26280900	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-10]
OMIM:616604	Chromosome 14q32 duplication syndrome, 700-kb		HP:0000006	PMID:26280900	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-10]
OMIM:616604	Chromosome 14q32 duplication syndrome, 700-kb		HP:0012325	PMID:26280900	PCS					P	HPO:probinson[2023-02-10]
OMIM:616604	Chromosome 14q32 duplication syndrome, 700-kb		HP:0011974	PMID:26280900	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-10]
OMIM:260565	Peho syndrome		HP:0000286	PMID:28335020	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0000341	PMID:28335020	PCS					P	HPO:probinson[2012-04-11];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0002521	PMID:28335020	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0010804	PMID:8460530	PCS					P	HPO:skoehler[2014-11-26];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001250	PMID:8723564	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001272	PMID:2070547	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0003196	PMID:2070547	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0006829	PMID:28335020	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001290	OMIM:260565	IEA					P	HPO:skoehler[2018-10-08]
OMIM:260565	Peho syndrome		HP:0007281	PMID:8301648	PCS					P	HPO:probinson[2012-04-11];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0012098	PMID:8723564	PCS					P	HPO:lccarmody[2018-09-24];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0008872	PMID:8301648	PCS					P	HPO:probinson[2012-04-11];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0007105	PMID:2070547	PCS					P	HPO:probinson[2012-04-11];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001302	OMIM:260565	TAS					P	HPO:skoehler[2017-07-13]
OMIM:260565	Peho syndrome		HP:0000278	PMID:2070547	IEA					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0007965	PMID:8301648	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001347	PMID:2070547	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0003469	PMID:8335020	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0000253	PMID:2070547	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0002079	OMIM:260565	TAS					P	HPO:skoehler[2017-07-13]
OMIM:260565	Peho syndrome		HP:0000194	PMID:2070547	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0000293	PMID:2070547	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001263	PMID:8460530	PCS					P	HPO:skoehler[2017-07-13];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001182	PMID:2070547	PCS					P	HPO:lccarmody[2018-09-24];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0000969	PMID:28335020	PCS					P	HPO:probinson[2012-04-11];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0000007	PMID:8301648	PCS					I	HPO:probinson[2009-02-17];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0002529	PMID:28335020	PCS					P	HPO:probinson[2012-04-11];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0000648	PMID:2070547	PCS					P	HPO:probinson[2012-04-11];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0002126	OMIM:260565	TAS					P	HPO:skoehler[2017-07-13]
OMIM:260565	Peho syndrome		HP:0007514	PMID:8723564	PCS					P	HPO:lccarmody[2018-09-24];HPO:lccarmody[2018-09-24]
OMIM:260565	Peho syndrome		HP:0001336	OMIM:260565	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0003456	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000684	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0004322	PMID:21488135	PCS		2/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0001156	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0001250	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0003472	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0010049	PMID:21488135	PCS		6/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0010743	OMIM:612462	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000939	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0100543	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000639	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000518	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0006297	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000311	PMID:21488135	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000135	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0001249	PMID:21488135	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000852	PMID:21488135	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0002135	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000293	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0003165	PMID:21488135	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000470	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0005280	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0002905	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000821	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0002925	PMID:21488135	PCS		6/6			P	HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0006960	OMIM:612462	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0002901	PMID:21488135	PCS		5/6			P	HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0001513	PMID:21488135	PCS		4/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-21]
OMIM:612462	Pseudohypoparathyroidism, type IC		HP:0000006	PMID:11788646	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-21]
OMIM:155200	Mediosternal depigmentation line		HP:0007581	OMIM:155200	IEA					P	HPO:iea[2009-02-17]
OMIM:155200	Mediosternal depigmentation line		HP:0000006	OMIM:155200	IEA					I	HPO:iea[2009-02-17]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0007902	OMIM:612304	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0003621	PMID:10942114	PCS		2/9			C	HPO:probinson[2022-09-09]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0005543	PMID:10942114	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-09]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0004850	PMID:10942114	PCS		4/9			P	HPO:probinson[2022-09-09]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0001250	OMIM:612304	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0001263	OMIM:612304	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0003593	PMID:10942114	PCS		1/9			C	HPO:probinson[2022-09-09];HPO:probinson[2022-09-09]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0100021	OMIM:612304	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0000979	OMIM:612304	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0100724	OMIM:612304	IEA					P	HPO:skoehler[2015-01-27]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0002638	OMIM:612304	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0000007	OMIM:612304	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0002204	OMIM:612304	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612304	Thrombophilia due to protein C deficiency, autosomal recessive		HP:0003623	PMID:10942114	PCS		6/9			C	HPO:probinson[2022-09-09]
OMIM:151700	Lipoma of the conjunctiva		HP:0012032	OMIM:151700	IEA					P	HPO:skoehler[2015-01-27]
OMIM:151700	Lipoma of the conjunctiva		HP:0012549	OMIM:151700	TAS					P	HPO:probinson[2014-01-01]
OMIM:151700	Lipoma of the conjunctiva		HP:0000006	OMIM:151700	TAS					I	HPO:probinson[2009-02-17]
OMIM:607084	Deafness, autosomal recessive 31		HP:0003577	PMID:15841483	PCS		4/4			C	HPO:probinson[2024-03-13]
OMIM:607084	Deafness, autosomal recessive 31		HP:0000407	PMID:12833159	PCS		6/6			P	HPO:probinson[2013-02-26];HPO:probinson[2024-03-13]
OMIM:607084	Deafness, autosomal recessive 31		HP:0000407	PMID:15841483	PCS	HP:0003577	4/4			P	HPO:probinson[2024-03-13]
OMIM:607084	Deafness, autosomal recessive 31		HP:0000007	PMID:12833159	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2024-03-13]
OMIM:607084	Deafness, autosomal recessive 31		HP:0008555	PMID:15841483	PCS		0/4			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-13]
OMIM:617297	Amelogenesis imperfecta, type IJ		HP:0000670	PMID:27843125	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617297	Amelogenesis imperfecta, type IJ		HP:0011094	PMID:27843125	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617297	Amelogenesis imperfecta, type IJ		HP:0000705	PMID:27843125	PCS					P	HPO:probinson[2019-09-03]
OMIM:617297	Amelogenesis imperfecta, type IJ		HP:0006297	PMID:27843125	PCS					P	HPO:probinson[2019-09-03]
OMIM:617297	Amelogenesis imperfecta, type IJ		HP:0000007	PMID:27843125	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617297	Amelogenesis imperfecta, type IJ		HP:0010299	PMID:27843125	PCS		0/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03];HPO:probinson[2024-03-15]
OMIM:617297	Amelogenesis imperfecta, type IJ		HP:0000687	PMID:27843125	PCS					P	HPO:probinson[2019-09-03]
OMIM:164750	Omphalocele due to duplication of 1p31.3		HP:0003577	PMID:22499347	PCS		9/9			C	HPO:probinson[2023-02-20]
OMIM:164750	Omphalocele due to duplication of 1p31.3		HP:0001539	PMID:22499347	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:164750	Omphalocele due to duplication of 1p31.3		HP:0000006	PMID:22499347	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-02-20]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0000365	OMIM:614946	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0003355	OMIM:614946	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001250	PMID:22833457	PCS		2/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002120	PMID:22833457	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001272	PMID:22833457	PCS		1/1			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001252	OMIM:614946	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0012707	PMID:22833457	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0025321	PMID:22833457	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0032794	PMID:22833457	PCS		2/2			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001903	OMIM:614946	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0007366	PMID:22833457	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002119	OMIM:614946	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001522	PMID:22833457	PCS		1/2			C	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0003623	PMID:22833457	PCS		2/2			C	HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0003128	PMID:22833457	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0006999	PMID:22833457	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0000252	PMID:22833457	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002059	PMID:22833457	PCS		1/1			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002353	OMIM:614946	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0025053	PMID:22833457	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0011968	PMID:22833457	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002151	PMID:22833457	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002490	PMID:22833457	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002171	OMIM:614946	TAS					P	HPO:skoehler[2013-01-21]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0012736	PMID:22833457	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0012465	PMID:22833457	PCS		1/1			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0003819	PMID:22833457	PCS		1/2			C	HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0002506	PMID:22833457	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0000007	PMID:22833457	PCS					I	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0000505	OMIM:614946	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001873	OMIM:614946	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001510	OMIM:614946	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0006568	PMID:22833457	PCS		1/2			P	HPO:probinson[2022-11-11]
OMIM:614946	Combined oxidative phosphorylation deficiency 14		HP:0001336	PMID:22833457	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-11-11]
OMIM:621057	Spermatogenic failure 97		HP:0034818	PMID:33332558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:6000135	PMID:33332558	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:0003251	PMID:33332558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:0011462	PMID:33332558	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:0045058	PMID:33332558	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:0025437	PMID:33332558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:0000007	PMID:33332558	PCS					I	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:0012208	PMID:33332558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:621057	Spermatogenic failure 97		HP:0032558	PMID:33332558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-08-30]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0001199	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0003038	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0005632	OMIM:201170	TAS					P	HPO:skoehler[2013-05-31]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0004322	OMIM:201170	IEA					P	HPO:iea[2009-02-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000260	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000160	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000316	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000954	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0001845	OMIM:201170	TAS					P	HPO:skoehler[2012-11-26]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000878	OMIM:201170	TAS					P	HPO:skoehler[2017-07-13]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0030084	OMIM:201170	IEA					P	HPO:skoehler[2018-10-08]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000218	OMIM:201170	IEA					P	HPO:skoehler[2019-02-22]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000358	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000431	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0001762	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000490	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0012165	OMIM:201170	TAS					P	HPO:skoehler[2013-02-25]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000448	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000007	OMIM:201170	IEA					I	HPO:iea[2009-02-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0001814	OMIM:201170	TAS					P	HPO:skoehler[2013-08-18]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000322	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0005736	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000347	OMIM:201170	IEA					P	HPO:iea[2009-02-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000963	OMIM:201170	IEA					P	HPO:iea[2009-02-17]
OMIM:201170	Acrofacial dysostosis syndrome of rodriguez		HP:0000369	OMIM:201170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613783	Complement component c1s deficiency		HP:0002725	OMIM:613783	TAS					P	HPO:probinson[2013-06-05]
OMIM:613783	Complement component c1s deficiency		HP:0000872	OMIM:613783	TAS					P	HPO:probinson[2013-01-09]
OMIM:613783	Complement component c1s deficiency		HP:0012115	OMIM:613783	TAS					P	HPO:probinson[2013-06-05]
OMIM:613783	Complement component c1s deficiency		HP:0005339	OMIM:613783	TAS					P	HPO:probinson[2013-06-05]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0003596	PMID:32846832	PCS		2/4			C	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0001639	PMID:32846832	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0011462	PMID:32846832	PCS		2/4			C	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0001681	PMID:32846832	PCS		3/7			P	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0005144	PMID:32846832	PCS		4/6			P	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0005110	PMID:32846832	PCS		1/6			P	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0002094	PMID:32846832	PCS		2/7			P	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0011712	PMID:32846832	PCS		1/6			P	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0012664	PMID:32846832	PCS		0/6			P	HPO:probinson[2022-07-04]
OMIM:115195	Cardiomyopathy, familial hypertrophic, 2		HP:0000006	OMIM:115195	IEA					I	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000341	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0007517	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000486	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000365	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0004322	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0002066	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0003298	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0001252	OMIM:268850	TAS					P	HPO:skoehler[2014-11-26]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0001290	OMIM:268850	TAS					P	HPO:skoehler[2017-07-13]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000639	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000717	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000612	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0001249	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000336	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000275	OMIM:268850	TAS					P	HPO:probinson[2012-05-01]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000252	OMIM:268850	TAS					P	HPO:probinson[2012-05-01]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000494	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000175	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000276	OMIM:268850	TAS					P	HPO:probinson[2012-05-01]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000490	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000272	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0009891	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0011297	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000508	OMIM:268850	TAS					P	HPO:probinson[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000767	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000007	OMIM:268850	IEA					I	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000601	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000625	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000565	OMIM:268850	TAS					P	HPO:skoehler[2013-03-27]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000204	OMIM:268850	IEA					P	HPO:iea[2009-02-17]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000248	OMIM:268850	TAS					P	HPO:probinson[2012-05-01]
OMIM:268850	Richieri-Costa/guion-Almeida syndrome		HP:0000303	OMIM:268850	TAS					P	HPO:skoehler[2017-07-13]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0010628	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003236	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003234	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0002240	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0001290	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0100293	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0001508	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0001427	PMID:19720722	PCS					I	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0000158	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0001324	OMIM:500009	TAS		12/20			P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003688	OMIM:500009;PMID:19720722	PCS		20/20			P	HPO:probinson[2017-06-24];HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003128	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003623	OMIM:500009	TAS					C	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0002058	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0001265	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003200	PMID:19720722	PCS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003542	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0011968	PMID:19720722	PCS		16/17			P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0002151	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0001284	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0009051	PMID:19720722	PCS		7/15			P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0009058	PMID:19720722	PCS		12/16			P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0002747	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0003737	OMIM:500009	IEA					P	HPO:skoehler[2015-01-27]
OMIM:500009	Mitochondrial myopathy, infantile, transient		HP:0000467	OMIM:500009	TAS					P	HPO:skoehler[2012-10-16]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001332	PMID:33443317	PCS		13/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000463	PMID:33443317	PCS		2/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001250	PMID:33443317	PCS		9/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001272	PMID:33443317	PCS		12/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0002263	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001252	PMID:33443317	PCS		14/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001270	PMID:33443317	PCS		13/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0033725	PMID:33443317	PCS		2/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000518	PMID:33443317	PCS		10/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000316	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0003429	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001249	PMID:33443317	PCS		14/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0002236	PMID:33443317	PCS		2/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0002553	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000252	PMID:33443317	PCS		4/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0002059	PMID:33443317	PCS		4/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000750	PMID:33443317	PCS		13/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0002376	PMID:33443317	PCS		5/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000012	PMID:33443317	PCS		2/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0011968	PMID:33443317	PCS		8/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000592	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001263	PMID:33443317	PCS		14/14			P	HPO:probinson[2021-06-14];HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0005280	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0010535	PMID:33443317	PCS		2/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000007	PMID:33443317	PCS					I	HPO:probinson[2021-06-14];HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000527	PMID:33443317	PCS		3/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0002307	PMID:33443317	PCS		7/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000664	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0002007	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0001257	PMID:33443317	PCS		13/15			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000369	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0009879	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:619286	Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia		HP:0000687	PMID:33443317	PCS		1/14			P	HPO:probinson[2021-06-14]
OMIM:309510	Partington syndrome		HP:0000750	OMIM:309510	IEA					P	HPO:iea[2009-02-17]
OMIM:309510	Partington syndrome		HP:0002353	OMIM:309510	IEA					P	HPO:iea[2009-02-17]
OMIM:309510	Partington syndrome		HP:0001250	PMID:15200506	PCS		12/40			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-03]
OMIM:309510	Partington syndrome		HP:0001371	OMIM:309510	IEA					P	HPO:iea[2009-02-17]
OMIM:309510	Partington syndrome		HP:0001260	PMID:15200506	PCS		15/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-03]
OMIM:309510	Partington syndrome		HP:0002451	OMIM:309510	IEA					P	HPO:skoehler[2010-06-20]
OMIM:309510	Partington syndrome		HP:0004373	PMID:15200506	PCS		21/34			P	HPO:probinson[2009-02-17];HPO:probinson[2020-08-03]
OMIM:309510	Partington syndrome		HP:0002061	OMIM:309510	IEA					P	HPO:iea[2009-02-17]
OMIM:309510	Partington syndrome		HP:0012469	PMID:15200506	IEA	HP:0003593	5/40			P	HPO:probinson[2020-08-03];HPO:probinson[2020-08-03]
OMIM:309510	Partington syndrome		HP:0012385	PMID:15200506	PCS		3/46			P	HPO:probinson[2020-08-03]
OMIM:309510	Partington syndrome		HP:0000708	PMID:15200506	PCS		8/28			P	HPO:probinson[2020-08-03]
OMIM:309510	Partington syndrome		HP:0001419	OMIM:309510	IEA					I	HPO:iea[2009-02-17]
OMIM:309510	Partington syndrome		HP:0000325	OMIM:309510	IEA					P	HPO:skoehler[2010-06-20]
OMIM:309510	Partington syndrome		HP:0001249	PMID:15200506	PCS		38/38	MALE		P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-03]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002421	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000882	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000243	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000485	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0004562	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003593	PMID:19659762	PCS		5/7			C	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001290	PMID:19659762	PCS		2/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001171	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0033725	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0008491	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001609	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001048	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002673	PMID:16116615	PCS		2/5			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0100540	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002827	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000767	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000403	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000007	PMID:16116615	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000341	OMIM:252500	TAS					P	HPO:probinson[2012-05-01]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000343	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003333	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000463	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002120	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002240	PMID:19659762	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0008070	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0008470	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001547	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0006610	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002756	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000212	PMID:19659762;PMID:16116615	PCS		5/12			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0011344	OMIM:252500	TAS					P	HPO:skoehler[2013-05-29]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003180	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000348	PMID:19659762	PCS		1/7			P	HPO:probinson[2012-05-01];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002804	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001319	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000347	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000105	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000286	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0007759	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001498	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001376	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003311	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001252	PMID:16116615	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001010	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000280	PMID:19659762;OMIM:252500	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0045075	OMIM:252500	TAS					P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0011463	PMID:19659762	PCS		1/7			C	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0011461	PMID:19659762	PCS		1/7			C	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000316	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0008850	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000158	PMID:19659762	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001265	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001540	PMID:19659762	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001385	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0030148	OMIM:252500	TAS					P	HPO:skoehler[2014-11-26]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001263	PMID:19659762;PMID:16116615	PCS		7/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002196	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0009092	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0012385	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001537	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002869	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001538	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001659	PMID:16116615	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001653	PMID:16116615	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003016	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002684	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000023	OMIM:252500	IEA		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001508	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000938	OMIM:252500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0008155	OMIM:252500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0030043	PMID:19659762;PMID:16116615	PCS		3/12			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002837	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0006532	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001744	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0009769	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0000154	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003026	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0008936	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003423	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001363	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001762	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003300	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0031936	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001640	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002299	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003264	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0002690	OMIM:252500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0005280	PMID:19659762	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003819	OMIM:252500	IEA					C	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001639	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0006362	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001635	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003538	OMIM:252500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0030051	PMID:16116615	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0004626	PMID:19659762	PCS		1/7			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0001510	PMID:19659762;PMID:16116615	PCS		5/12			P	HPO:probinson[2022-05-08]
OMIM:252500	Mucolipidosis II alpha/beta		HP:0003414	OMIM:252500	IEA					P	HPO:iea[2009-02-17]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0001760	OMIM:618198	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0002015	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0003577	PMID:26752647	PCS		1/1			C	HPO:probinson[2022-11-27]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0000750	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0001762	PMID:26752647	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0031936	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0011968	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0005684	PMID:26752647	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0001270	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0002093	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0012385	PMID:26752647	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-27]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0006380	PMID:26752647	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0000639	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0000508	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0000657	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0000602	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0000007	PMID:26752647	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0001558	OMIM:618198	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0001324	OMIM:618198	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618198	Myasthenic syndrome, congenital, 24, presynaptic		HP:0002104	OMIM:618198	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0004325	PMID:21575681	PCS		3/3			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001176	PMID:16538222	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000486	PMID:15586325;OMIM:300534	PCS		11/29			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001773	PMID:21575681	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0004322	PMID:18697827;PMID:19826449;PMID:21575681	PCS		13/18			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25];HPO:probinson[2022-07-10]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001250	PMID:18697827;PMID:19826449;PMID:15586325	PCS		8/35			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001371	PMID:19826449	PCS		1/6			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000319	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0011463	PMID:31419599	PCS		3/3			C	HPO:probinson[2022-08-23]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000718	PMID:18697827;PMID:19826449;PMID:15586325;PMID:21575681	PCS		13/38			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000711	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0008734	PMID:18697827;PMID:15586325	PCS		3/29			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000752	PMID:21575681	PCS		3/3			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001249	PMID:19826449;PMID:15586325	PCS		25/26			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000297	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000054	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000252	PMID:18697827;PMID:19826449;PMID:31419599;PMID:21575681	PCS		7/20			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0002232	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000574	PMID:19826449	PCS		1/6			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0003487	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0002395	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000490	PMID:15586325	PCS		1/20			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001263	PMID:21575681	PCS		3/3			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001419	PMID:15586325	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000327	PMID:15586325;PMID:21575681	PCS		7/23			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000767	PMID:16538222	PCS		2/2			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0008124	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000400	PMID:16538222	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0002788	PMID:21575681	PCS		3/3			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001257	PMID:15586325	PCS		7/20			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000582	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001156	OMIM:300534	TAS					P	HPO:skoehler[2014-11-26]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000540	PMID:15586325	PCS		3/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000221	PMID:16538222	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0002362	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001270	PMID:31419599	PCS		3/3			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0010864	PMID:16538222;PMID:31419599;PMID:21575681	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25];HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0007020	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001508	PMID:21575681	PCS		3/3			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0007021	PMID:15586325	PCS		2/20			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0009882	OMIM:300534	TAS					P	HPO:probinson[2013-04-13]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000219	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0006895	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000218	PMID:18697827;PMID:21575681	PCS		6/12			P	HPO:probinson[2012-04-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000411	PMID:19826449	PCS		3/6			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000256	PMID:15586325	PCS		2/20			P	HPO:skoehler[2013-06-23];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000699	PMID:16538222;PMID:15586325	PCS		6/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001347	PMID:19826449	PCS		3/6			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001762	OMIM:300534	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000750	PMID:31419599	PCS		3/3			P	HPO:probinson[2022-08-23]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000350	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0001081	PMID:15586325	PCS		2/20			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0032792	PMID:31419599	PCS		1/3			P	HPO:probinson[2022-08-23]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000426	PMID:19826449	PCS		2/6			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000744	OMIM:300534	IEA					P	HPO:iea[2009-02-17]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0002967	PMID:16538222	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0002205	PMID:21575681	PCS		3/3			P	HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000028	PMID:15586325	PCS		2/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000303	PMID:15586325	PCS		2/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000347	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0000545	PMID:15586325	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300534	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type		HP:0008944	OMIM:300534	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618826	Retinitis pigmentosa 88		HP:0007737	PMID:31833436	PCS	HP:0011463	3/3			P	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12]
OMIM:618826	Retinitis pigmentosa 88		HP:0000662	PMID:31833436	PCS		3/3			P	HPO:probinson[2020-05-12]
OMIM:618826	Retinitis pigmentosa 88		HP:0000608	PMID:31236346	PCS		1/1			P	HPO:probinson[2021-02-25]
OMIM:618826	Retinitis pigmentosa 88		HP:0000007	PMID:30025130	PCS					I	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12]
OMIM:618826	Retinitis pigmentosa 88		HP:0007663	PMID:31833436;PMID:31236346	PCS		4/4			P	HPO:probinson[2021-02-25];HPO:probinson[2020-05-12];HPO:probinson[2020-05-12]
OMIM:618826	Retinitis pigmentosa 88		HP:0011505	PMID:31833436	PCS					P	HPO:probinson[2020-05-12]
OMIM:618826	Retinitis pigmentosa 88		HP:0000543	PMID:31833436;PMID:31236346	PCS		4/4			P	HPO:probinson[2021-02-25];HPO:probinson[2020-05-12];HPO:probinson[2021-02-25]
OMIM:618826	Retinitis pigmentosa 88		HP:0007843	PMID:31833436;PMID:31236346	PCS		4/4			P	HPO:probinson[2021-02-25];HPO:probinson[2020-05-12]
OMIM:618826	Retinitis pigmentosa 88		HP:0000577	PMID:31236346	PCS		1/1			P	HPO:probinson[2021-02-25]
OMIM:618826	Retinitis pigmentosa 88		HP:0003623	PMID:31236346	PCS		1/1			C	HPO:probinson[2021-02-25]
OMIM:184840	Stickler syndrome, type III		HP:0000175	OMIM:184840	IEA					P	HPO:iea[2009-02-17]
OMIM:184840	Stickler syndrome, type III		HP:0000463	PMID:15372529	PCS		27/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:184840	Stickler syndrome, type III		HP:0003088	PMID:15372529	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:184840	Stickler syndrome, type III		HP:0000272	PMID:15372529	PCS		27/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:184840	Stickler syndrome, type III		HP:0011800	OMIM:184840	TAS					P	HPO:skoehler[2013-11-28]
OMIM:184840	Stickler syndrome, type III		HP:0005280	PMID:15372529	PCS		27/28			P	HPO:probinson[2022-09-23]
OMIM:184840	Stickler syndrome, type III		HP:0010580	OMIM:184840	IEA					P	HPO:iea[2009-02-17]
OMIM:184840	Stickler syndrome, type III		HP:0002829	PMID:15372529;OMIM:184840	PCS		20/20			P	HP:probinson[2018-04-16];HPO:probinson[2022-09-23];HPO:iea[2009-02-17]
OMIM:184840	Stickler syndrome, type III		HP:0000407	PMID:15372529	PCS		16/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:184840	Stickler syndrome, type III		HP:0000926	OMIM:184840	IEA					P	HPO:iea[2009-02-17]
OMIM:184840	Stickler syndrome, type III		HP:0002656	OMIM:184840	IEA					P	HPO:iea[2009-02-17]
OMIM:184840	Stickler syndrome, type III		HP:0000201	OMIM:184840	IEA					P	HPO:iea[2009-02-17]
OMIM:184840	Stickler syndrome, type III		HP:0000006	PMID:15372529	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:184840	Stickler syndrome, type III		HP:0000478	PMID:15372529	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-23]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000286	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0004325	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000582	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0001891	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0002521	PMID:12684507	PCS		1/1			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0002188	PMID:12684507	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0004322	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0001332	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0003593	PMID:12684507;PMID:33644825	PCS		3/4			C	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0002240	PMID:12684507	PCS		1/1			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0002020	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0001290	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0001270	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0012368	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0033725	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0012469	PMID:12684507	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0001929	PMID:12684507	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0007183	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000639	PMID:12684507	PCS		1/1			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000518	PMID:33644825	PCS					P	HPO:skoehler[2015-03-22];HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0011463	PMID:33644825	PCS		1/3			C	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000817	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000612	PMID:12684507	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0020045	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0002119	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000218	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0003645	PMID:12684507	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0001347	OMIM:607906	TAS					P	HPO:skoehler[2015-03-22]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0003642	PMID:12684507	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0002014	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000252	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000431	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000750	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0001382	PMID:33644825	PCS		2/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0003186	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0011344	PMID:12684507;PMID:33644825	PCS		4/4			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0011097	PMID:33644825	PCS		3/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0012520	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000407	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0040288	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000821	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000007	PMID:12684507	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000505	PMID:12684507	PCS		1/1			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-06-15]
OMIM:607906	Congenital disorder of glycosylation, type Ii		HP:0000369	PMID:33644825	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:256000	Leigh syndrome		HP:0003676	OMIM:256000	TAS					C	HPO:skoehler[2012-11-26]
OMIM:256000	Leigh syndrome		HP:0000486	OMIM:256000	TAS					P	HPO:skoehler[2015-07-26]
OMIM:256000	Leigh syndrome		HP:0001332	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001250	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001252	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001251	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0003593	OMIM:256000	IEA					C	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0000580	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001290	OMIM:256000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:256000	Leigh syndrome		HP:0033249	PMID:21611066	PCS					P	HPO:probinson[2021-02-13]
OMIM:256000	Leigh syndrome		HP:0001508	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0000639	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0011463	PMID:21611066	PCS		2/2			C	HPO:probinson[2021-02-13]
OMIM:256000	Leigh syndrome		HP:0000712	OMIM:256000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256000	Leigh syndrome		HP:0000998	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001427	OMIM:256000	IEA					I	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001404	OMIM:256000	TAS					P	HPO:skoehler[2012-11-26]
OMIM:256000	Leigh syndrome		HP:0002878	OMIM:256000	TAS					P	HPO:skoehler[2014-06-24]
OMIM:256000	Leigh syndrome		HP:0007305	OMIM:256000	PCS					P	HPO:probinson[2012-04-11]
OMIM:256000	Leigh syndrome		HP:0001249	OMIM:256000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256000	Leigh syndrome		HP:0001347	OMIM:256000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256000	Leigh syndrome		HP:0003128	OMIM:256000	PCS					P	HPO:probinson[2012-04-11]
OMIM:256000	Leigh syndrome		HP:0002793	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001260	OMIM:256000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256000	Leigh syndrome		HP:0001263	OMIM:256000	PCS		20/20			P	HPO:skoehler[2019-02-22];HPO:probinson[2012-04-11]
OMIM:256000	Leigh syndrome		HP:0002151	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0002171	OMIM:256000	PCS		20/20			P	HPO:probinson[2012-04-11];HPO:skoehler[2012-11-26]
OMIM:256000	Leigh syndrome		HP:0002490	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0002093	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0000407	PMID:22114105	PCS					P	HPO:iea[2009-08-31];HP:probinson[2019-01-03]
OMIM:256000	Leigh syndrome		HP:0000508	OMIM:256000	TAS					P	HPO:skoehler[2015-07-26]
OMIM:256000	Leigh syndrome		HP:0000602	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0000007	OMIM:256000	IEA					I	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0000648	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:256000	Leigh syndrome		HP:0001257	OMIM:256000	IEA					P	HPO:iea[2009-02-17]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0000365	PMID:24136862	PCS		5/14			P	HP:probinson[2019-03-09]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0000518	PMID:25159689;PMID:24136862	PCS		37/45			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];HP:probinson[2019-03-09]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0007663	PMID:15342707	PCS					P	HPO:skoehler[2015-07-26];HP:probinson[2019-03-01]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0000648	PMID:15342707;PMID:24136862	PCS		24/24			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];HP:probinson[2019-03-09]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0002071	PMID:15342707	PCS				HP:0012825	P	HPO:skoehler[2014-01-28];HP:probinson[2019-03-01]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0000543	PMID:24136862	PCS		11/14			P	HP:probinson[2019-03-09]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0000575	PMID:24136862	PCS		9/9			P	HP:probinson[2019-03-09]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0000006	PMID:15342707	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:165300	Optic atrophy 3, autosomal dominant		HP:0001337	PMID:15342707	PCS				HP:0012825	P	HPO:skoehler[2014-01-28];HP:probinson[2019-03-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003236	PMID:36745799	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003596	PMID:36745799	PCS		6/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003155	PMID:36745799	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0025168	PMID:36745799	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0410174	PMID:36745799	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0030099	PMID:37167966	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003593	PMID:37167966	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0010602	PMID:37167966	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0100297	PMID:37167966	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0031964	PMID:36745799	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0040081	PMID:36745799	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0011463	PMID:37167966	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003803	PMID:37167966	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003701	PMID:37167966	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003327	PMID:37167966	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0009129	PMID:36745799	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003326	PMID:37167966	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0001265	PMID:36745799	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003687	PMID:37167966	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0031956	PMID:36745799	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0002015	PMID:36745799	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0004379	PMID:36745799	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003621	PMID:37167966	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0002098	PMID:36745799	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0410263	PMID:36745799	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0001284	PMID:36745799	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0002093	PMID:36745799	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0008981	PMID:37167966	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0012240	PMID:37167966	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0007210	PMID:36745799	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0003738	PMID:36745799	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0000007	PMID:37167966	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0002505	PMID:37167966;PMID:36745799	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0002747	PMID:37167966	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0001315	PMID:37167966	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620375	Muscular dystrophy, limb-girdle, autosomal recessive 28		HP:0004887	PMID:36745799	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:618832	Epilepsy, early-onset, with or without developmental delay		HP:0002069	PMID:31197650	PCS	HP:0003593	4/4			P	HPO:probinson[2020-07-21]
OMIM:618832	Epilepsy, early-onset, with or without developmental delay		HP:0002188	PMID:31197650	PCS		1/4			P	HPO:probinson[2020-07-21]
OMIM:618832	Epilepsy, early-onset, with or without developmental delay		HP:0000034	PMID:31197650	PCS		1/2	MALE		P	HPO:probinson[2020-07-21]
OMIM:618832	Epilepsy, early-onset, with or without developmental delay		HP:0001263	PMID:31197650	PCS		1/3			P	HPO:probinson[2020-07-21]
OMIM:618832	Epilepsy, early-onset, with or without developmental delay		HP:0000006	PMID:31197650	PCS					I	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618832	Epilepsy, early-onset, with or without developmental delay		HP:0001655	PMID:31197650	PCS		1/4			P	HPO:probinson[2020-07-21]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0002268	PMID:22101681	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-08]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0003621	PMID:22101681	PCS		33/33			C	HPO:probinson[2023-05-08]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0002310	OMIM:128200	IEA					P	HPO:iea[2009-02-17]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0001250	PMID:22101681	PCS		0/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-05-08]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0007098	PMID:22101681	PCS					P	HPO:probinson[2012-07-16];HPO:probinson[2023-05-08]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0003829	OMIM:128200	TAS					I	HPO:skoehler[2012-11-25]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0000006	PMID:22101681	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-08]
OMIM:128200	Episodic kinesigenic dyskinesia 1		HP:0012469	PMID:22101681	PCS		2/32			P	HPO:probinson[2023-05-08]
OMIM:212130	Cardiomyopathy associated with myopathy and sudden death		HP:0003198	OMIM:212130	IEA					P	HPO:iea[2009-02-17]
OMIM:212130	Cardiomyopathy associated with myopathy and sudden death		HP:0001670	OMIM:212130	IEA					P	HPO:iea[2009-02-17]
OMIM:212130	Cardiomyopathy associated with myopathy and sudden death		HP:0000007	OMIM:212130	IEA					I	HPO:iea[2009-02-17]
OMIM:192950	Vertical talus, congenital		HP:0001838	OMIM:192950	IEA					P	HPO:iea[2009-02-17]
OMIM:192950	Vertical talus, congenital		HP:0001848	OMIM:192950	IEA					P	HPO:iea[2009-02-17]
OMIM:192950	Vertical talus, congenital		HP:0008138	OMIM:192950	IEA					P	HPO:iea[2009-02-17]
OMIM:192950	Vertical talus, congenital		HP:0000006	OMIM:192950	IEA					I	HPO:iea[2009-02-17]
OMIM:192950	Vertical talus, congenital		HP:0001369	OMIM:192950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611816	Temple-Baraitser syndrome		HP:0000286	PMID:25420144	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0000343	PMID:25420144	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0001250	PMID:25420144	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0002000	PMID:25420144	PCS		5/6			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0001252	PMID:25420144	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0002020	PMID:25420144	PCS		1/5			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0003593	PMID:25420144	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0012553	PMID:25420144	PCS		4/6			P	HPO:probinson[2014-01-04];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0010055	PMID:25420144	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0012471	PMID:25420144	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0009882	PMID:25420144	PCS		5/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0000316	PMID:25420144	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0001847	PMID:25420144	PCS		6/6			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0009623	PMID:25420144	PCS		6/6			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0002714	PMID:25420144	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0002019	PMID:25420144	PCS		2/5			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0001642	PMID:25420144	PCS		1/2			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0002058	PMID:25420144	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0000154	PMID:25420144	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0009928	PMID:25420144	PCS		1/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0001263	PMID:25420144	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0001181	PMID:25420144	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0012554	PMID:25420144	PCS		2/6			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0012555	PMID:25420144	PCS		5/6			P	HPO:probinson[2014-01-04];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0005280	PMID:25420144	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0011304	PMID:25420144	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0009693	PMID:25420144	PCS		4/6			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0001631	PMID:25420144	PCS		1/2			P	HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0000006	PMID:25420144	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0004425	PMID:25420144	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-17]
OMIM:611816	Temple-Baraitser syndrome		HP:0000445	OMIM:611816	IEA					P	HPO:iea[2009-02-17]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0007814	PMID:15914600	PCS					P	HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0030632	PMID:15914600	PCS					P	HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0000662	PMID:15914600	PCS					P	HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0000551	PMID:15914600	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0000639	OMIM:304020	TAS					P	HPO:skoehler[2010-06-20]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0011462	PMID:15914600	PCS		10/10	MALE		C	HPO:probinson[2022-04-30]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0000613	PMID:15914600	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0007663	PMID:15914600	PCS			MALE		P	HPO:skoehler[2015-07-26];HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0000505	PMID:15914600	PCS			MALE		P	HPO:iea[2009-02-17];HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0001417	PMID:15914600	PCS					I	HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0007722	PMID:15914600	PCS					P	HPO:probinson[2020-07-23]
OMIM:304020	Cone-rod dystrophy, X-linked, 1		HP:0000545	PMID:15914600	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-23]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0001056	OMIM:131750	TAS					P	HPO:probinson[2009-02-17]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0003577	PMID:8170945	PCS		12/14			C	HPO:probinson[2009-02-17];HPO:probinson[2023-02-26]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0033803	PMID:8170945	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0002164	OMIM:131750	TAS					P	HPO:probinson[2012-07-31]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0008066	PMID:8170945	PCS		14/14			P	HPO:probinson[2012-07-31];HPO:probinson[2023-02-26]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0001075	OMIM:131750	TAS					P	HPO:probinson[2009-02-17]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0008404	OMIM:131750	TAS					P	HPO:skoehler[2013-05-03]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0000006	PMID:8170945	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-26]
OMIM:131750	Epidermolysis bullosa dystrophica, autosomal dominant		HP:0003623	PMID:8170945	PCS		2/14			C	HPO:probinson[2023-02-26]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0000121	PMID:36571463	PCS		6/11			P	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0003621	PMID:36571463	PCS		2/6			C	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0003159	PMID:36571463	PCS		5/11			P	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0003596	PMID:36571463	PCS		1/6			C	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0003584	PMID:36571463	PCS		1/6			C	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0011462	PMID:36571463	PCS		2/6			C	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0012405	PMID:36571463	PCS		4/11			P	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0000006	PMID:36571463	PCS					I	HPO:probinson[2023-07-17]
OMIM:620374	Nephrolithiasis, calcium oxalate, 2, with nephrocalcinosis		HP:0000787	PMID:36571463	PCS		5/11			P	HPO:probinson[2023-07-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000175	OMIM:246560	TAS					P	HPO:skoehler[2012-10-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000089	OMIM:246560	TAS					P	HPO:skoehler[2012-10-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0002164	OMIM:246560	TAS					P	HPO:skoehler[2012-10-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000160	OMIM:246560	IEA					P	HPO:iea[2009-02-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0001171	OMIM:246560	IEA					P	HPO:skoehler[2015-01-27]
OMIM:246560	Split-Hand/foot malformation 3		HP:0012385	OMIM:246560	TAS					P	HPO:skoehler[2013-10-22]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000308	OMIM:246560	IEA					P	HPO:iea[2009-02-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0001807	OMIM:246560	TAS					P	HPO:skoehler[2013-05-31]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000327	OMIM:246560	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000007	OMIM:246560	IEA					I	HPO:iea[2009-02-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000218	OMIM:246560	TAS					P	HPO:skoehler[2012-10-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0008404	OMIM:246560	TAS					P	HPO:skoehler[2013-05-03]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000377	OMIM:246560	TAS					P	HPO:skoehler[2012-10-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000545	OMIM:246560	IEA					P	HPO:iea[2009-02-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0001249	OMIM:246560	IEA					P	HPO:iea[2009-02-17]
OMIM:246560	Split-Hand/foot malformation 3		HP:0000006	OMIM:246560	TAS					I	HPO:skoehler[2012-10-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0003577	PMID:20089953	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0002540	PMID:19781681;PMID:20089953	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000260	PMID:19781681;PMID:20089953	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0005474	PMID:21282188	PCS					P	HP:probinson[2019-04-13]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0003593	PMID:20089953	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000939	PMID:19781681;PMID:20089953	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0006094	PMID:19781681	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000938	PMID:19781681;PMID:20089953	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0008873	PMID:19781681;PMID:20089953	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-26];HPO:iea[2009-02-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0002757	PMID:19781681;PMID:20089953	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-26];HPO:iea[2009-02-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000774	PMID:20089953	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0002953	PMID:20089953	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0001763	PMID:20089953	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0005469	PMID:20089953	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0002650	PMID:21282188;PMID:19781681	PCS		11/12			P	HPO:iea[2009-02-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0003023	PMID:21282188;PMID:19781681	PCS		14/14			P	HPO:iea[2009-02-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000592	PMID:19781681	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-27]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0002194	PMID:19781681;PMID:20089953	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0045087	PMID:19781681	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0002808	PMID:19781681	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0034198	PMID:19781681	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000926	PMID:21282188	PCS	HP:0030674				P	HP:probinson[2019-04-13];HP:probinson[2019-04-13]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0006385	PMID:21282188	PCS	HP:0003577				P	HP:probinson[2019-04-13]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000767	OMIM:259440	IEA					P	HPO:iea[2009-02-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0001537	PMID:19781681;PMID:20089953	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000007	PMID:21282188	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-13]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0006640	PMID:21282188	PCS	HP:0003577				P	HP:probinson[2019-04-13]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0006487	PMID:20089953	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000703	PMID:19781681;OMIM:259440	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-06-26];HPO:iea[2009-02-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000768	OMIM:259440	IEA					P	HPO:iea[2009-02-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0002645	PMID:19781681	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000520	PMID:20089953	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0000325	PMID:20089953	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0005019	PMID:20089953	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:259440	Osteogenesis imperfecta, type IX		HP:0005855	PMID:19781681;PMID:20089953	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-06-26];HPO:iea[2009-02-17]
OMIM:178350	Pubic bone dysplasia		HP:0000924	OMIM:178350	IEA					P	HPO:iea[2009-02-17]
OMIM:178350	Pubic bone dysplasia		HP:0000006	OMIM:178350	IEA					I	HPO:iea[2009-02-17]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000286	PMID:32694869	PCS		14/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001250	PMID:32694869	PCS		3/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001371	PMID:32694869	PCS		6/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002263	PMID:32694869	PCS		8/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001252	PMID:32694869	PCS		9/12			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002020	PMID:32694869	PCS		4/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0045075	PMID:32694869	PCS		11/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0033725	PMID:32694869	PCS		1/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0012110	PMID:32694869	PCS		1/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000316	PMID:32694869	PCS		8/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001643	PMID:32694869	PCS		1/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001763	PMID:32694869	PCS		4/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001249	PMID:32694869	PCS		14/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000358	PMID:32694869	PCS		1/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002553	PMID:32694869	PCS		10/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001385	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000010	PMID:32694869	PCS		1/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000574	PMID:32694869	PCS		1/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002750	PMID:32694869	PCS		1/6			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001382	PMID:32694869	PCS		3/12			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0011968	PMID:32694869	PCS		2/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001263	PMID:32694869	PCS		14/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000691	PMID:32694869	PCS		1/12			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000294	PMID:32694869	PCS		3/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001182	PMID:32694869	PCS		8/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0010751	PMID:32694869	PCS		6/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0100025	PMID:32694869	PCS		1/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000729	PMID:32694869	PCS		1/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000805	PMID:32694869	PCS		1/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002308	PMID:32694869	PCS		1/9			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000689	PMID:32694869	PCS		1/12			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000527	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0004209	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002307	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000047	PMID:32694869	PCS		1/7			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000322	PMID:32694869	PCS		4/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000006	PMID:32694869	PCS					I	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000369	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000687	PMID:32694869	PCS		4/12			P	HPO:probinson[2021-06-02];HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000445	PMID:32694869	PCS		4/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000066	PMID:32694869	PCS		1/5			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000463	PMID:32694869	PCS		3/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000581	PMID:32694869	PCS		14/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0010624	PMID:32694869	PCS		4/11			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0012368	PMID:32694869	PCS		5/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000418	PMID:32694869	PCS		4/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0009882	PMID:32694869	PCS		2/12			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0006297	PMID:32694869	PCS		1/12			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000733	PMID:32694869	PCS		1/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002837	PMID:32694869	PCS		3/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000219	PMID:32694869	PCS		12/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0006532	PMID:32694869	PCS		1/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000653	PMID:32694869	PCS		11/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000154	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000750	PMID:32694869	PCS		9/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002650	PMID:32694869	PCS		3/12			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001762	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000431	PMID:32694869	PCS		10/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0031936	PMID:32694869	PCS		10/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000430	PMID:32694869	PCS		7/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0045025	PMID:32694869	PCS		10/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000508	PMID:32694869	PCS		2/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002209	PMID:32694869	PCS		4/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000744	PMID:32694869	PCS		2/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0001357	PMID:32694869	PCS		3/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000664	PMID:32694869	PCS		4/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0002007	PMID:32694869	PCS		7/14			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0007018	PMID:32694869	PCS		1/13			P	HPO:probinson[2021-06-02]
OMIM:619293	Blepharophimosis-impaired intellectual development syndrome		HP:0000028	PMID:32694869	PCS		3/7			P	HPO:probinson[2021-06-02]
OMIM:219070	Curved nail of fourth toe		HP:0008393	OMIM:219070	IEA					P	HPO:iea[2009-02-17]
OMIM:219070	Curved nail of fourth toe		HP:0009882	OMIM:219070	IEA					P	HPO:iea[2009-02-17]
OMIM:219070	Curved nail of fourth toe		HP:0001812	OMIM:219070	IEA					P	HPO:iea[2009-02-17]
OMIM:219070	Curved nail of fourth toe		HP:0000007	OMIM:219070	IEA					I	HPO:iea[2009-02-17]
OMIM:187390	Tendons, extensor, of fingers, anomalous insertion of		HP:0001167	OMIM:187390	TAS					P	HPO:iea[2009-02-17]
OMIM:187390	Tendons, extensor, of fingers, anomalous insertion of		HP:0000006	OMIM:187390	IEA					I	HPO:iea[2009-02-17]
OMIM:618827	Myopia 27		HP:0011003	PMID:30689892	PCS	HP:0011463	7/8			P	HPO:probinson[2020-03-31];HPO:probinson[2020-03-31]
OMIM:618827	Myopia 27		HP:0000006	PMID:30689892	PCS					I	HPO:probinson[2020-03-31];HPO:probinson[2020-03-31]
OMIM:618827	Myopia 27		HP:0007800	PMID:30689892	PCS		3/3			P	HPO:probinson[2020-03-31]
OMIM:207500	Anus, imperforate		HP:0002023	OMIM:207500	IEA					P	HPO:iea[2009-02-17];HPO:nvasilevsky[2019-03-12]
OMIM:207500	Anus, imperforate		HP:0000007	OMIM:207500	TAS					I	HPO:nvasilevsky[2019-03-12];HPO:nvasilevsky[2019-03-12]
OMIM:207500	Anus, imperforate		HP:0001426	PMID:4852015	TAS					I	HPO:nvasilevsky[2019-03-12];HPO:nvasilevsky[2019-03-12]
OMIM:601386	Deafness, autosomal recessive 12		HP:0001751	PMID:17850630	PCS		0/6			P	HPO:probinson[2023-03-30]
OMIM:601386	Deafness, autosomal recessive 12		HP:0000007	PMID:17850630	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-30]
OMIM:601386	Deafness, autosomal recessive 12		HP:0000510	PMID:17850630	PCS		0/6			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-30]
OMIM:601386	Deafness, autosomal recessive 12		HP:0000399	PMID:17850630	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-30]
OMIM:621056	TIMES syndrome		HP:0000582	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000483	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0003577	PMID:39623139	PCS		2/2			C	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0002023	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000563	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000463	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0004322	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0001250	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0003196	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0034697	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0100255	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000938	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0002757	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000378	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0002239	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000010	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000252	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0002353	PMID:39623139	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000750	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000490	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0004692	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0004691	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000822	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000965	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000821	PMID:39623139	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000601	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000648	PMID:39623139	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000505	PMID:39623139	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0002604	PMID:39623139	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0001257	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000545	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000501	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000787	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:6001182	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000006	PMID:39623139	PCS					I	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621056	TIMES syndrome		HP:0000621	PMID:39623139	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0003676	PMID:27817865	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001332	PMID:27817865	PCS		12/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0002063	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001252	PMID:27817865	PCS		2/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000580	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001251	PMID:27817865	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0012179	PMID:27817865	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000639	PMID:27817865	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001508	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0011463	PMID:27817865	PCS		5/7			C	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0007166	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000514	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0007663	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001347	PMID:27817865	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0003621	PMID:27817865	PCS		2/7			C	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0002015	PMID:27817865	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0002312	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001288	PMID:27817865	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0003487	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0003121	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0011968	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0025312	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001260	PMID:27817865	PCS		14/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0002072	PMID:27817865	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0002194	PMID:27817865	PCS		2/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0100660	PMID:27817865	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000007	PMID:27817865	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000505	PMID:27817865	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000648	PMID:27817865	PCS	HP:0003621	6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000648	PMID:27817865	PCS		5/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0002505	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000543	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001257	PMID:27817865	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0002305	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0004305	PMID:27817865	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0001336	PMID:27817865	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities		HP:0000643	PMID:27817865	PCS		1/7			P	HPO:probinson[2022-10-30]
OMIM:203000	Frontonasal dysplasia with alar clefts		HP:0000430	OMIM:203000	IEA					P	HPO:iea[2009-02-17]
OMIM:203000	Frontonasal dysplasia with alar clefts		HP:0000506	OMIM:203000	IEA					P	HPO:iea[2009-02-17]
OMIM:203000	Frontonasal dysplasia with alar clefts		HP:0000007	OMIM:203000	IEA					I	HPO:iea[2009-02-17]
OMIM:203000	Frontonasal dysplasia with alar clefts		HP:0003191	OMIM:203000	IEA					P	HPO:iea[2009-02-17]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0003236	PMID:11901181	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0003577	PMID:11901181	PCS		1/1			C	HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0031956	PMID:11901181	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0003198	PMID:11901181	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0003199	PMID:11901181	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0001252	PMID:11901181	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0001263	PMID:11901181	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0003160	PMID:11901181	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0000007	PMID:11901181	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0001305	PMID:11901181	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0000238	PMID:11901181	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0000256	PMID:11901181	PCS	HP:0003577	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:607091	Congenital disorder of glycosylation, type IID		HP:0003645	PMID:11901181	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:164745	Omodysplasia 2		HP:0000066	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0003577	PMID:25759469	PCS		2/2			C	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0003038	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0010804	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0006429	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0030016	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000343	PMID:25759469	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0001076	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0002020	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0005792	PMID:25759469	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000060	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0010034	OMIM:164745	IEA					P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0000316	PMID:25759469	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0006376	OMIM:164745	TAS					P	HPO:probinson[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0000358	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000456	OMIM:164745	IEA					P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0000396	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000175	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000054	OMIM:164745	IEA					P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0002650	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000431	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0003762	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0011968	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0005025	OMIM:164745	IEA					P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0004573	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0004991	PMID:25759469	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0003083	PMID:25759469	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0005280	PMID:25759469	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0005060	OMIM:164745	TAS					P	HPO:skoehler[2010-06-18]
OMIM:164745	Omodysplasia 2		HP:0100336	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000403	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0004209	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0002007	OMIM:164745	IEA					P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0000047	OMIM:164745	IEA					P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0000006	PMID:25759469	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:164745	Omodysplasia 2		HP:0000028	OMIM:164745	IEA					P	HPO:iea[2009-02-17]
OMIM:164745	Omodysplasia 2		HP:0000347	PMID:25759469	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0003761	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0001662	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0003781	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0000707	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0000007	OMIM:208155	IEA					I	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0002804	OMIM:208155	TAS					P	HPO:probinson[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0005968	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0000201	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0002104	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:208155	Arthrogryposis multiplex congenita with whistling face		HP:0000346	OMIM:208155	IEA					P	HPO:iea[2009-02-17]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0012265	PMID:23993197	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0002257	PMID:23993197	PCS		10/12			P	HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0001696	PMID:23993197	PCS		0/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0002110	PMID:23993197	PCS		9/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0012263	PMID:23993197	PCS		1/12			P	HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0000789	PMID:23993197	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0033036	PMID:23993197	PCS		4/5			P	HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0000007	PMID:23993197	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0000403	PMID:23993197	PCS		8/12			P	HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0006510	PMID:23993197	PCS		3/12			P	HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0011108	PMID:23993197	PCS		10/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-19]
OMIM:615481	Ciliary dyskinesia, primary, 24		HP:0002643	PMID:23993197	PCS	HP:0003623	4/12			P	HPO:probinson[2023-01-19]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0002344	PMID:21907147	PCS		3/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000486	PMID:21907147	PCS		1/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000023	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0004322	OMIM:614947	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001250	PMID:21907147	PCS		1/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001252	OMIM:614947	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001251	PMID:21907147	PCS		1/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0100543	OMIM:614947	TAS				HP:0012825	P	HPO:skoehler[2014-05-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000639	OMIM:614947	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001629	OMIM:614947	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000954	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0007663	PMID:21907147	PCS		2/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0002317	OMIM:614947	TAS					P	HPO:skoehler[2014-07-11]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0005943	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0002311	PMID:21907147	PCS		1/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000252	OMIM:614947	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0030765	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000750	OMIM:614947	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001263	PMID:21907147	PCS		3/3		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0002151	PMID:21907147	PCS		1/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0005144	OMIM:614947	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0005165	PMID:21907147	PCS		2/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0002490	PMID:21907147	PCS		3/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0011923	PMID:21907147	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001716	PMID:21907147	PCS		2/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000822	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0007256	PMID:21907147	PCS		1/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000007	PMID:21907147	PCS					I	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0007334	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0008347	PMID:21907147	PCS		3/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000648	PMID:21907147	PCS		1/3			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0000543	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0200055	PMID:21907147	PCS		1/3			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0002500	OMIM:614947	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001513	OMIM:614947	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:614947	Combined oxidative phosphorylation deficiency 15		HP:0001337	OMIM:614947	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000483	PMID:27005418	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000486	PMID:27005418	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0002188	PMID:27005418	PCS		1/3			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000540	PMID:27005418	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0003593	PMID:27005418	PCS		1/3			C	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0002064	PMID:29667355	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001093	PMID:29667355	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0007082	PMID:27005418	PCS		2/3			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000639	PMID:27005418	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0011220	PMID:27005418	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0011461	PMID:27005418	PCS		2/3			C	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0007663	PMID:27005418	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000678	PMID:27005418	PCS		1/3			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0006895	PMID:29667355	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001249	PMID:27005418	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001347	PMID:27005418	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0008936	PMID:27005418	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0002059	PMID:27005418	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0006956	PMID:27005418	PCS	HP:0011461	3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001561	PMID:27005418	PCS	HP:0011461	1/2			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000750	PMID:29667355;PMID:27005418	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000293	PMID:29667355;PMID:27005418	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0025335	PMID:29667355	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000490	PMID:27005418	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001263	PMID:29667355;PMID:27005418	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0002509	PMID:27005418	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001338	PMID:27005418	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0030051	PMID:29667355	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000565	PMID:27005418	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001258	PMID:27005418	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001357	PMID:27005418	PCS		3/3			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0002007	PMID:27005418	PCS		1/3			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000322	PMID:29667355	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000006	PMID:27005418	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0001513	PMID:29667355;PMID:27005418	PCS		3/4			P	HPO:probinson[2021-09-05];HPO:skoehler[2019-09-07];HPO:probinson[2021-09-05]
OMIM:617296	Spastic paraplegia, intellectual disability, nystagmus, and obesity		HP:0000248	PMID:27005418	PCS		3/3			P	HPO:probinson[2021-09-05]
OMIM:130300	Electroencephalographic peculiarity: fronto-precentral beta wave groups		HP:0002353	OMIM:130300	IEA					P	HPO:skoehler[2009-02-17]
OMIM:130300	Electroencephalographic peculiarity: fronto-precentral beta wave groups		HP:0000006	OMIM:130300	IEA					I	HPO:iea[2009-02-17]
OMIM:616188	Retinal dystrophy and obesity		HP:0000483	PMID:24375934	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0003621	PMID:24375934	PCS		1/1			C	HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0000541	PMID:24375934	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0032027	PMID:24375934	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0500087	PMID:24375934	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0007663	PMID:24375934	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0000007	PMID:24375934	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0000505	PMID:24375934	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0007722	PMID:24375934	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0007843	PMID:24375934	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0001513	PMID:24375934	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0000545	PMID:24375934	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-06]
OMIM:616188	Retinal dystrophy and obesity		HP:0000556	PMID:24375934	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-06]
OMIM:179700	Red cell phospholipid defect with hemolysis		HP:0001046	PMID:3090825	PCS					P	HPO:lccarmody[2018-09-11]
OMIM:179700	Red cell phospholipid defect with hemolysis		HP:0002904	OMIM:179700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:179700	Red cell phospholipid defect with hemolysis		HP:0001923	OMIM:179700	IEA					P	HPO:iea[2009-02-17]
OMIM:179700	Red cell phospholipid defect with hemolysis		HP:0000006	OMIM:179700	IEA					I	HPO:iea[2009-02-17]
OMIM:179700	Red cell phospholipid defect with hemolysis		HP:0001744	PMID:3090825	PCS				HP:0012826	P	HPO:lccarmody[2018-09-11]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001298	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0002465	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0003355	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001250	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0003593	PMID:11157507	PCS					C	HPO:iea[2009-02-17]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001251	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001290	OMIM:603585	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0040185	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000639	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0002718	PMID:11157507	PCS					P	HPO:iea[2009-02-17]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0030084	OMIM:603585	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001249	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0005469	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001265	OMIM:603585	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000252	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0002310	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000490	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001260	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001263	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0031156	OMIM:603585	TAS					P	HPO:probinson[2018-03-05]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000093	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0040223	PMID:11157507	PCS					P	HPO:probinson[2017-06-16]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001933	PMID:11157507	PCS					P	HPO:probinson[2017-06-16]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000007	PMID:11157507	PCS					I	HPO:iea[2009-02-17]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000601	OMIM:603585	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001659	OMIM:603585	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001873	PMID:11157507	PCS					P	HPO:probinson[2017-06-16]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000322	OMIM:603585	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0000465	OMIM:603585	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603585	Congenital disorder of glycosylation, type IIf		HP:0001875	PMID:11157507	PCS					P	HPO:probinson[2017-06-16]
OMIM:613796	Mycobacterial and viral infections, susceptibility to, autosomal recessive		HP:0011274	OMIM:613796	TAS					P	HPO:probinson[2013-06-05]
OMIM:613796	Mycobacterial and viral infections, susceptibility to, autosomal recessive		HP:0000007	OMIM:613796	TAS					I	HPO:probinson[2013-06-05]
OMIM:613796	Mycobacterial and viral infections, susceptibility to, autosomal recessive		HP:0004429	OMIM:613796	TAS					P	HPO:probinson[2013-06-05]
OMIM:613796	Mycobacterial and viral infections, susceptibility to, autosomal recessive		HP:0012302	OMIM:613796	TAS					P	HPO:probinson[2013-01-09]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0003126	PMID:29654216	PCS		28/28			P	HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0004322	OMIM:134600	IEA					P	HPO:iea[2009-02-17]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0003355	PMID:29654216	PCS		28/28			P	HPO:skoehler[2019-04-18]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0000083	PMID:29654216	PCS	HP:0011462				P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0003155	PMID:29654216	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0003076	PMID:29654216	PCS		28/28			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0034359	PMID:29654216	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0011463	PMID:29654216	PCS		28/28			C	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0002748	PMID:29654216	PCS		0/28			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0002749	OMIM:134600	IEA					P	HPO:iea[2009-02-17]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0002900	PMID:29654216	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0003648	OMIM:134600	IEA					P	HPO:iea[2009-02-17]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0003109	PMID:29654216	PCS		28/28			P	HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0001324	OMIM:134600	TAS	HP:0003581				P	HPO:skoehler[2010-06-20]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0000124	PMID:29654216	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0000006	PMID:29654216	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0002148	PMID:29654216	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:134600	Fanconi renotubular syndrome 1		HP:0001942	PMID:29654216	PCS		28/28			P	HPO:probinson[2023-03-31]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000684	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0001156	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0004322	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000293	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000470	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0010049	OMIM:612463	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0005280	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0010743	OMIM:612463	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000939	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0100543	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000518	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000639	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0006297	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000311	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000006	PMID:2122458	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-25]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0001513	OMIM:612463	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0001249	OMIM:612463	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612463	Pseudopseudohypoparathyroidism		HP:0000852	OMIM:612463	IEA					P	HPO:skoehler[2015-01-19]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0004446	OMIM:153670	IEA					P	HPO:iea[2009-02-17]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0000132	PMID:1730088	PCS		2/2	FEMALE		P	HPO:probinson[2012-07-17];HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0031364	PMID:1730088	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0011877	PMID:1730088	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0031128	PMID:1730088	PCS		0/3			P	HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0011871	PMID:1730088	PCS		3/3			P	HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0001878	OMIM:153670	IEA					P	HPO:iea[2009-02-17]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0006298	PMID:1730088	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0000967	OMIM:153670	IEA					P	HPO:iea[2009-02-17]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0000978	OMIM:153670	IEA					P	HPO:iea[2009-02-17]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0000421	PMID:1730088	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0001873	PMID:1730088	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0000006	PMID:1730088	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0001744	OMIM:153670	IEA				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0004866	PMID:1730088	PCS		0/3			P	HPO:probinson[2023-02-11]
OMIM:153670	Bernard-Soulier syndrome, type A2, autosomal dominant		HP:0000225	OMIM:153670	IEA					P	HPO:iea[2009-02-17]
OMIM:601379	Hunter-Mcalpine craniosynostosis syndrome		HP:0001363	OMIM:601379	IEA					P	HPO:iea[2009-02-17]
OMIM:601379	Hunter-Mcalpine craniosynostosis syndrome		HP:0004322	OMIM:601379	IEA					P	HPO:iea[2009-02-17]
OMIM:601379	Hunter-Mcalpine craniosynostosis syndrome		HP:0000160	OMIM:601379	PCS					P	HPO:iea[2009-02-17]
OMIM:601379	Hunter-Mcalpine craniosynostosis syndrome		HP:0007874	OMIM:601379	IEA					P	HPO:iea[2009-02-17]
OMIM:601379	Hunter-Mcalpine craniosynostosis syndrome		HP:0002714	OMIM:601379	PCS					P	HPO:iea[2012-02-26]
OMIM:601379	Hunter-Mcalpine craniosynostosis syndrome		HP:0000006	OMIM:601379	IEA					I	HPO:iea[2009-02-17]
OMIM:601379	Hunter-Mcalpine craniosynostosis syndrome		HP:0001249	OMIM:601379	IEA					P	HPO:iea[2009-02-17]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0001041	OMIM:308800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000491	OMIM:308800	PCS					P	HPO:iea[2012-03-02]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0004552	OMIM:308800	PCS					P	HPO:iea[2012-03-01]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0001131	OMIM:308800	IEA					P	HPO:iea[2009-02-17]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0025084	OMIM:308800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0045075	OMIM:308800	TAS					P	HPO:probinson[2022-05-08]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0008391	OMIM:308800	PCS					P	HPO:iea[2012-03-02]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000958	OMIM:308800	IEA					P	HPO:iea[2009-02-17]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0032152	OMIM:308800	IEA					P	HPO:skoehler[2019-02-22]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0001419	PMID:20672378	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2022-05-08]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000509	OMIM:308800	PCS					P	HPO:iea[2012-03-02]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0030054	OMIM:308800	TAS					P	HPO:skoehler[2014-09-21]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000613	OMIM:308800	PCS					P	HPO:iea[2012-03-02]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000656	OMIM:308800	PCS					P	HPO:probinson[2009-02-17]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000653	OMIM:308800	PCS					P	HPO:iea[2012-03-01]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0008404	OMIM:308800	TAS					P	HPO:probinson[2022-08-08]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000498	OMIM:308800	IEA					P	HPO:iea[2009-02-17]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0007502	OMIM:308800	PCS					P	HPO:iea[2012-03-02]
OMIM:308800	Keratosis follicularis spinulosa decalvans, X-linked		HP:0000982	OMIM:308800	PCS					P	HPO:iea[2012-03-02]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0001276	OMIM:264070	IEA					P	HPO:skoehler[2010-06-20]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0008297	PMID:9585615	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0033594	PMID:9585615	PCS		13/13			P	HPO:probinson[2021-02-13]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0001290	PMID:9585615	PCS		2/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0000007	PMID:9585615	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0001270	PMID:9585615	PCS		1/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-01-30]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0004923	PMID:9585615	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-01-30]
OMIM:264070	Hyperphenylalaninemia, BH4-deficient, D		HP:0001337	OMIM:264070	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0003774	PMID:15265795	PCS		3/3			P	HPO:probinson[2013-03-26];HPO:probinson[2022-06-06]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0012221	PMID:15265795	PCS		3/3			P	HPO:probinson[2013-03-30];HPO:probinson[2022-06-06]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0000123	PMID:15265795	PCS					P	HPO:probinson[2013-03-26]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0000407	PMID:15265795	PCS		3/3			P	HPO:probinson[2013-03-26];HPO:probinson[2022-06-06]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0033485	PMID:15265795	PCS		1/1			P	HPO:probinson[2022-06-06]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0000007	PMID:15265795	PCS					I	HPO:probinson[2013-03-26]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0008404	PMID:15265795	PCS					P	HPO:probinson[2013-03-26]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0007678	PMID:15265795	PCS					P	HPO:probinson[2013-03-26]
OMIM:609057	Nephropathy with pretibial epidermolysis bullosa and deafness		HP:0004722	PMID:15265795	PCS		1/1			P	HPO:probinson[2022-06-06]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0003577	PMID:32439809	PCS		11/11			C	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0010804	PMID:32439809	PCS		4/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0002224	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000343	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0001250	PMID:32439809	PCS		1/11			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0001274	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0001252	PMID:32439809	PCS		6/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0007082	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000958	PMID:32439809	PCS		2/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000718	PMID:32439809	PCS		2/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000337	PMID:32439809	PCS		2/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000219	PMID:32439809	PCS		5/8			P	HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0025336	PMID:32439809	PCS		8/9			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000218	PMID:32439809	PCS		2/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0006610	PMID:32439809	PCS		3/6			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0001249	PMID:32439809	PCS		10/10			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0001007	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0002553	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0002059	PMID:32439809	PCS		8/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0006956	PMID:32439809	PCS		7/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000252	PMID:32439809	PCS		6/11			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000750	PMID:32439809	PCS		11/11			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0001344	PMID:32439809	PCS		6/11			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000276	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0025335	PMID:32439809	PCS		10/11			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0002352	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000294	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0011229	PMID:32439809	PCS		2/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0007371	PMID:32439809	PCS		7/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0002808	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000729	PMID:32439809	PCS		2/11			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000448	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000007	PMID:32439809	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000307	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000322	PMID:32439809	PCS		2/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000369	PMID:32439809	PCS		3/8			P	HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000248	PMID:32439809	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0000028	PMID:32439809	PCS		2/5			P	HPO:probinson[2022-02-27]
OMIM:619244	Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism		HP:0009879	PMID:32439809	PCS		7/8			P	HPO:probinson[2022-02-27]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0010628	OMIM:301830	TAS					P	HPO:skoehler[2012-11-16]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0003236	PMID:31932168	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0000023	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001371	OMIM:301830	TAS					P	HPO:probinson[2012-05-05]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0003198	OMIM:301830	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001252	OMIM:301830	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0006829	OMIM:301830	TAS					P	HPO:skoehler[2012-11-16]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001308	OMIM:301830	TAS		1/1			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0007269	OMIM:301830	TAS					P	HPO:skoehler[2015-01-21]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0003623	PMID:31932168	PCS		1/1			C	HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0002058	OMIM:301830	TAS		1/1			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0000054	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0002650	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0002398	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001284	OMIM:301830	TAS		1/1			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0002093	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0032988	PMID:31932168	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0033383	PMID:31932168	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001419	PMID:18179898	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-20]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001939	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0002828	OMIM:301830	TAS					P	HPO:skoehler[2012-11-16]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0000508	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0002804	OMIM:301830	TAS					P	HPO:skoehler[2012-11-16]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001558	OMIM:301830	TAS					P	HPO:skoehler[2012-11-16]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0002747	OMIM:301830	TAS					P	HPO:skoehler[2012-11-16]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0000047	OMIM:301830	TAS					P	HPO:skoehler[2012-11-16]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0000028	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0000347	OMIM:301830	IEA					P	HPO:iea[2009-02-17]
OMIM:301830	Spinal muscular atrophy, X-linked 2		HP:0001612	PMID:31932168	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000286	PMID:32891193	PCS		6/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0002267	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001773	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0002144	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0004322	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001250	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001252	PMID:32891193	PCS		3/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0003196	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000041	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0030011	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0003593	PMID:32891193	PCS					C	HPO:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0012227	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0009381	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0010490	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0012471	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0008499	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000316	PMID:32891193	PCS		3/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000954	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001800	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001643	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001249	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000358	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000494	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0033737	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000252	PMID:32891193	PCS		4/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0002870	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0011968	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001382	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001263	PMID:32891193	PCS		9/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001182	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000729	PMID:32891193	PCS		5/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000805	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0004209	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000125	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000047	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0009778	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000006	PMID:32891193	PCS					I	HPO:probinson[2021-10-27];HPO:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000369	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000325	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000126	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000385	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0031923	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000463	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000540	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000020	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001629	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0008551	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000414	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000733	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0002714	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000218	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000455	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000670	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0002015	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000475	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000750	PMID:32891193	PCS		4/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0003189	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0002650	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000431	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000034	PMID:32891193	PCS		1/8	MALE		P	HP:probinson[2021-10-27];HPO:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000074	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0045025	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000709	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001837	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000506	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0009237	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001511	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001631	PMID:32891193	PCS		4/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0007018	PMID:32891193	PCS		3/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0001510	PMID:32891193	PCS		1/19			P	HP:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000028	PMID:32891193	PCS		1/8	MALE		P	HP:probinson[2021-10-27];HPO:probinson[2021-10-27]
OMIM:619522	Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities		HP:0000104	PMID:32891193	PCS		2/19			P	HP:probinson[2021-10-27]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0002155	OMIM:245900	IEA					P	HPO:iea[2009-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0003233	OMIM:245900	TAS					P	HPO:probinson[2009-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0003651	OMIM:245900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0000083	OMIM:245900	IEA					P	HPO:iea[2009-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0025433	PMID:2370048	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0001084	PMID:2370048	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0003581	PMID:2370048	PCS		1/1			C	HPO:probinson[2023-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0001878	OMIM:245900	IEA					P	HPO:iea[2009-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0000007	PMID:2370048	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0000093	PMID:2370048	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:245900	Lecithin:cholesterol acyltransferase deficiency		HP:0001895	OMIM:245900	IEA					P	HPO:iea[2009-02-17]
OMIM:133190	Spinocerebellar ataxia 34		HP:0001265	PMID:24566826	PCS		7/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0003477	PMID:24566826	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0003596	PMID:24566826	PCS		5/13			C	HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0001272	PMID:24566826	PCS		6/9			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0002120	PMID:24566826	PCS		4/9			P	HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0001260	PMID:24566826	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0002066	PMID:24566826	PCS		12/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0003584	PMID:24566826	PCS		5/13			C	HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0001251	OMIM:133190	IEA					P	HPO:iea[2009-02-17]
OMIM:133190	Spinocerebellar ataxia 34		HP:0002075	OMIM:133190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133190	Spinocerebellar ataxia 34		HP:0002380	OMIM:133190	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:133190	Spinocerebellar ataxia 34		HP:0002070	PMID:24566826	PCS		9/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0002080	OMIM:133190	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:133190	Spinocerebellar ataxia 34		HP:0000639	PMID:24566826	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0000605	OMIM:133190	IEA					P	HPO:skoehler[2018-10-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0011462	PMID:24566826	PCS		3/13			C	HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0003829	OMIM:133190	TAS					I	HPO:skoehler[2015-12-30]
OMIM:133190	Spinocerebellar ataxia 34		HP:0007772	PMID:24566826	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0007256	OMIM:133190	IEA					P	HPO:skoehler[2018-10-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0001019	PMID:24566826	PCS		14/19			P	HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0001257	OMIM:133190	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:133190	Spinocerebellar ataxia 34		HP:0000006	PMID:24566826	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0001347	OMIM:133190	IEA					P	HPO:skoehler[2018-10-08]
OMIM:133190	Spinocerebellar ataxia 34		HP:0000962	PMID:24566826	PCS		14/19			P	HPO:probinson[2024-12-03]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0003621	PMID:31201888	PCS		1/3			C	HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0025708	PMID:31201888	PCS		2/3			C	HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0001818	PMID:31201888	PCS		3/3			P	HPO:probinson[2022-11-21];HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0000007	PMID:31201888	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0001954	PMID:31201888	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0002722	PMID:31201888	PCS		3/3			P	HPO:probinson[2022-11-21];HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0000421	PMID:31201888	PCS		3/3			P	HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0040238	PMID:31201888	PCS		3/3			P	HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0002027	PMID:31201888	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0011107	PMID:31201888	PCS		3/3			P	HPO:probinson[2022-11-21]
OMIM:260570	Immunodeficiency 108 with autoinflammation		HP:0011447	PMID:31201888	PCS		3/3			P	HPO:probinson[2022-11-21]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:6000473	PMID:20301297	PCS					P	HPO:probinson[2024-04-03]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001596	PMID:30443250	PCS		10/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0003212	PMID:30385752;PMID:30443250	PCS		102/111			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001250	PMID:30443250	PCS		12/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0003593	PMID:30443250	PCS					C	HPO:probinson[2022-05-09]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0100651	PMID:30443250	PCS		43/88			P	HPO:skoehler[2013-05-31];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0100651	PMID:30385752	PCS	HP:0003593	7/28			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001508	PMID:30443250	PCS		66/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001903	PMID:30443250	PCS		29/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0002958	PMID:30443250	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0002716	PMID:30443250	PCS		12/88			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0002119	PMID:30443250	PCS		3/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001369	PMID:30443250	PCS		8/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0000099	PMID:30385752	PCS		3/28			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001880	PMID:30385752	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0002595	OMIM:304790	TAS					P	HPO:iea[2009-02-17]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001263	PMID:30443250	PCS		12/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0032169	PMID:30443250	PCS		41/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0012115	PMID:30385752	PCS		4/28			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001419	PMID:30443250	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0011473	PMID:30443250	PCS		40/88			P	HPO:skoehler[2013-06-04];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0500093	PMID:30385752;PMID:30443250	PCS		42/116			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0000964	PMID:30385752;PMID:30443250	PCS		97/116			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0000821	PMID:30385752	PCS		2/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001019	PMID:30385752;PMID:30443250	PCS		9/116			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001973	PMID:30385752	PCS		2/28			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001873	PMID:30443250	PCS		19/88			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0004844	PMID:30385752	PCS		4/28			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0001875	PMID:30443250	PCS		11/88			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0002028	PMID:30385752	PCS		28/28			P	HPO:probinson[2020-09-30]
OMIM:304790	Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked		HP:0025329	PMID:30385752	PCS		9/28			P	HPO:probinson[2020-09-30]
OMIM:613769	Retinitis pigmentosa 44		HP:0001133	PMID:10581022	PCS					P	HPO:probinson[2013-06-05];HPO:probinson[2020-07-22]
OMIM:613769	Retinitis pigmentosa 44		HP:0000007	PMID:10581022	PCS					I	HPO:probinson[2020-07-22]
OMIM:613769	Retinitis pigmentosa 44		HP:0000505	PMID:10581022	PCS					P	HPO:probinson[2013-06-05];HPO:probinson[2020-07-22]
OMIM:613769	Retinitis pigmentosa 44		HP:0000510	PMID:10581022	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-22]
OMIM:613769	Retinitis pigmentosa 44		HP:0007843	PMID:10581022	PCS					P	HPO:probinson[2013-06-05];HPO:probinson[2020-07-22]
OMIM:613769	Retinitis pigmentosa 44		HP:0000006	PMID:10581022	PCS					I	HPO:probinson[2013-06-05];HPO:probinson[2020-07-22]
OMIM:613769	Retinitis pigmentosa 44		HP:0000654	PMID:10581022	PCS					P	HPO:probinson[2013-06-05];HPO:probinson[2020-07-22]
OMIM:610248	Deafness, autosomal recessive 65		HP:0000365	OMIM:610248	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610248	Deafness, autosomal recessive 65		HP:0003593	OMIM:610248	IEA					C	HPO:skoehler[2010-06-19]
OMIM:610248	Deafness, autosomal recessive 65		HP:0000007	OMIM:610248	IEA					I	HPO:skoehler[2010-06-19]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0001265	PMID:12566280	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0004336	PMID:12566280	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0003621	PMID:12566280	PCS		5/9			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0002015	PMID:12566280	PCS		1/9			P	HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0003431	PMID:12566280	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0001761	PMID:12566280	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0003693	PMID:12566280	PCS		8/8			P	HPO:probinson[2012-07-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0003383	PMID:12566280	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0001263	PMID:12566280	PCS		1/9			P	HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0001284	PMID:12566280	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0002460	PMID:12566280	PCS		9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0003593	PMID:12566280	PCS		1/9			C	HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0003481	PMID:12566280	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0001270	PMID:12566280	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0003380	OMIM:607734	IEA					P	HPO:iea[2009-02-17]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0011463	PMID:12566280	PCS		3/9			C	HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0007233	OMIM:607734	IEA					P	HPO:iea[2009-02-17]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0000007	PMID:12566280	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0002936	PMID:12566280	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0000006	OMIM:607734	IEA					I	HPO:iea[2009-02-17]
OMIM:607734	Charcot-Marie-Tooth disease, demyelinating, type 1F		HP:0001337	PMID:12566280	PCS		2/9			P	HPO:probinson[2022-09-02]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002267	PMID:28007986	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0010804	OMIM:617527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002188	PMID:28413018;PMID:28007986	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001250	PMID:28007986	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0430046	PMID:28007986	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0004485	PMID:28413018	PCS		6/6			P	HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0003196	PMID:28413018	PCS		1/7			P	HPO:skoehler[2019-04-18]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002063	OMIM:617527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001252	PMID:28413018	PCS		13/15			P	HPO:probinson[2019-08-29];HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0003593	PMID:28007986	PCS		7/7			C	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000280	PMID:28413018	PCS		7/7			P	HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0033725	PMID:28413018;PMID:28007986	PCS		11/12			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000639	PMID:28413018	PCS		4/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000319	PMID:28413018	PCS		1/7			P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000954	PMID:28413018	PCS		3/7			P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0100807	OMIM:617527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002536	PMID:28413018	PCS		10/10			P	HPO:probinson[2019-08-29];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000358	PMID:28413018	PCS		2/7			P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001007	PMID:28413018;PMID:28007986	PCS		6/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-29];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000253	PMID:28007986	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0007109	PMID:28413018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002553	PMID:28413018	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001344	PMID:28413018	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002079	PMID:28007986	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0003487	PMID:28007986	PCS		5/7			P	HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002197	PMID:28413018;PMID:28007986	PCS		8/12			P	HPO:probinson[2019-08-29];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0011968	PMID:28413018	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002033	OMIM:617527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000490	PMID:28413018	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001263	PMID:28413018;PMID:28007986	PCS		14/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0005781	PMID:28007986	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002194	PMID:28413018	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002071	PMID:28007986	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0100259	PMID:28413018	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0006980	PMID:28413018	PCS		9/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000007	PMID:28007986	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000648	PMID:28413018	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000768	PMID:28413018	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000369	PMID:28413018	PCS		3/7			P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0007514	PMID:28413018	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002104	PMID:28413018	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000341	PMID:28413018	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001276	PMID:28413018	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0003577	PMID:28413018;PMID:28007986	PCS		17/17			C	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000343	PMID:28413018	PCS		1/7			P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002120	PMID:28413018;PMID:28007986	PCS		14/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002483	PMID:28413018	PCS		7/10			P	HPO:probinson[2019-08-29];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0010862	PMID:28413018	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0100543	PMID:28413018	PCS		8/8			P	HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001508	PMID:28007986	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0012098	PMID:28413018	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000338	OMIM:617527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002119	PMID:28413018;PMID:28007986	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-04-22];HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000218	PMID:28413018	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000851	PMID:28413018	PCS		1/7			P	HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001561	PMID:28413018	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002015	OMIM:617527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000750	PMID:28007986	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001283	PMID:28413018	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0034964	PMID:28413018	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002093	OMIM:617527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0001838	PMID:28007986	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0002808	PMID:28007986	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0007410	PMID:28413018	PCS		6/7			P	HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0007256	PMID:28007986	PCS		7/7			P	HPO:probinson[2019-08-29]
OMIM:617527	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies		HP:0000347	PMID:28413018	PCS		1/7			P	HPO:skoehler[2018-10-08]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0000695	OMIM:601345	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0001597	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0004322	OMIM:601345	IEA				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0004482	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0045075	OMIM:601345	TAS					P	HPO:probinson[2022-05-08];HPO:probinson[2022-07-10]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0100038	OMIM:601345	TAS					P	HPO:skoehler[2012-03-01]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0000968	OMIM:601345	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0000668	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0002209	OMIM:601345	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0007387	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0000956	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0000653	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0000006	OMIM:601345	IEA					I	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0000677	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0004437	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:601345	Ectodermal dysplasia with natal teeth, Turnpenny type		HP:0007515	OMIM:601345	IEA					P	HPO:iea[2009-02-17]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0001771	PMID:31853710	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0003236	PMID:28754666	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0033748	PMID:31853710	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0002166	PMID:28754666;PMID:31853710	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0000365	PMID:31853710	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0003596	PMID:28754666;PMID:31853710	PCS		2/7			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0003551	PMID:31853710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0002063	PMID:31853710	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0012548	PMID:31853710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0040081	PMID:31853710	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0011462	PMID:28754666;PMID:31853710	PCS		5/7			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0001962	PMID:28754666	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0003448	PMID:31853710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0007328	PMID:31853710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0002650	PMID:31853710	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0008959	PMID:28754666	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0001761	PMID:31853710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0001288	PMID:31853710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0006937	PMID:28754666;PMID:31853710	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0003484	PMID:31853710	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0003383	PMID:31853710	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0012515	PMID:31853710	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0033383	PMID:28754666;PMID:31853710	PCS		6/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0012046	PMID:31853710	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0009053	PMID:28754666;PMID:31853710	PCS		5/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0040126	PMID:31853710	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0009830	PMID:31853710	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0000762	PMID:28754666	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0002522	PMID:31853710	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0000006	PMID:28754666	PCS					I	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621095	Charcot-Marie-Tooth disease, axonal, type 2JJ		HP:0008944	PMID:31853710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0001298	PMID:23462291	PCS					P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0003577	PMID:23462291	PCS		2/2			C	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0003676	OMIM:615330	IEA					C	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0001250	OMIM:615330	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0012706	PMID:23462291	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0001252	PMID:23462291	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0006829	OMIM:615330	TAS					P	HPO:skoehler[2013-09-10]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0032653	PMID:23462291	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:6000830	OMIM:615330	TAS					P	HPO:probinson[2024-08-03]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0032480	PMID:23462291	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0100543	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000639	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000737	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0008314	PMID:23462291	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002878	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002119	PMID:23462291	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000218	PMID:23462291	PCS		1/2			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0006610	PMID:23462291	PCS		1/2			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002415	PMID:23462291	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000278	PMID:23462291	PCS		1/2			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0001942	PMID:23462291	PCS					P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0003128	PMID:23462291	PCS		1/1			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002059	PMID:23462291	PCS		1/1			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0003324	PMID:23462291	PCS		1/2			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000252	PMID:23462291	PCS		2/2			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0001561	PMID:23462291	PCS		2/2			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002510	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002376	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002079	PMID:23462291	PCS		1/1			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0011968	PMID:23462291	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002154	PMID:23462291	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002490	PMID:23462291	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0011923	PMID:23462291	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002093	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0500230	PMID:23462291	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002804	PMID:23462291	PCS		2/2			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000007	PMID:23462291	PCS					I	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0001954	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000648	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0000505	OMIM:615330	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0001511	PMID:23462291	PCS		2/2			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:615330	Multiple mitochondrial dysfunctions syndrome 3		HP:0002126	PMID:23462291	PCS		1/1			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-02-26]
OMIM:228520	Fibrochondrogenesis 1		HP:0003038	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000882	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0001773	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000485	OMIM:228520	TAS					P	HPO:probinson[2012-05-08]
OMIM:228520	Fibrochondrogenesis 1		HP:0005257	PMID:21035103	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0000160	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0003196	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0008451	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0001804	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0003826	OMIM:228520	IEA					C	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0001800	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0005622	OMIM:228520	TAS					P	HPO:probinson[2012-05-08]
OMIM:228520	Fibrochondrogenesis 1		HP:0000175	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000890	OMIM:228520	TAS					P	HPO:probinson[2012-05-27]
OMIM:228520	Fibrochondrogenesis 1		HP:0012385	OMIM:228520	TAS					P	HPO:skoehler[2013-10-22]
OMIM:228520	Fibrochondrogenesis 1		HP:0000926	PMID:21035103	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0000007	PMID:21035103	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0001539	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0004209	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000922	PMID:21035103	PCS					P	HPO:probinson[2012-06-10];HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0001538	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000520	PMID:21035103	PCS					P	HPO:probinson[2012-05-08];HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0000883	OMIM:228520	TAS					P	HPO:probinson[2012-05-27]
OMIM:228520	Fibrochondrogenesis 1		HP:0000369	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0001655	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0003577	PMID:21035103	PCS		3/3			C	HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0000343	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0008905	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000463	PMID:21035103	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0000260	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0005476	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0003375	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0003175	OMIM:228520	TAS					P	HPO:probinson[2012-05-28]
OMIM:228520	Fibrochondrogenesis 1		HP:0012368	OMIM:228520	IEA					P	HPO:skoehler[2018-10-08]
OMIM:228520	Fibrochondrogenesis 1		HP:0100865	OMIM:228520	TAS					P	HPO:probinson[2012-05-28]
OMIM:228520	Fibrochondrogenesis 1		HP:0001789	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000377	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000773	PMID:21035103	PCS					P	HPO:probinson[2012-05-27];HPO:probinson[2022-10-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0003026	OMIM:228520	TAS					P	HPO:probinson[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0004279	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0005442	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000272	OMIM:228520	IEA					P	HPO:skoehler[2010-06-20]
OMIM:228520	Fibrochondrogenesis 1		HP:0000470	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0005280	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0000907	OMIM:228520	TAS					P	HPO:probinson[2012-06-10]
OMIM:228520	Fibrochondrogenesis 1		HP:0000947	OMIM:228520	TAS					P	HPO:probinson[2012-05-08]
OMIM:228520	Fibrochondrogenesis 1		HP:0009473	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0002007	OMIM:228520	IEA					P	HPO:iea[2009-02-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0200055	OMIM:228520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:228520	Fibrochondrogenesis 1		HP:0006645	OMIM:228520	TAS					P	HPO:probinson[2009-02-17]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0002155	PMID:18710388;PMID:16582076	PCS		31/31			P	HPO:probinson[2020-10-31];HPO:probinson[2013-01-07];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001250	PMID:18710388	PCS		1/14			P	HPO:skoehler[2014-02-25];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001263	PMID:18710388	PCS		1/14			P	HPO:skoehler[2014-02-25];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001252	PMID:16582076	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-31]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0002240	PMID:18710388;PMID:16582076	PCS		21/21			P	HPO:probinson[2013-01-07];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0003593	PMID:18710388	PCS		11/28			C	HPO:probinson[2020-10-31];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0011900	PMID:18710388;PMID:16582076	PCS		29/31			P	HPO:probinson[2020-10-31];HPO:probinson[2013-01-07];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0003281	PMID:18710388;PMID:16582076	PCS		13/14			P	HPO:probinson[2013-01-07];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0012156	PMID:18710388;PMID:16582076	PCS		18/21			P	HPO:probinson[2020-10-31];HPO:probinson[2013-01-07]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0000969	PMID:18710388	PCS		5/14			P	HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001903	PMID:16582076	PCS		7/7			P	HPO:probinson[2013-01-07]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0011463	PMID:18710388	PCS		5/14			C	HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0000509	PMID:16582076	PCS		1/7			P	HPO:probinson[2020-10-31]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0000007	PMID:16582076	PCS					I	HPO:probinson[2013-01-07]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0002716	PMID:18710388	PCS		8/13			P	HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001954	PMID:18710388	PCS		14/14			P	HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001945	PMID:18710388;PMID:16582076	PCS		24/24			P	HPO:probinson[2020-10-31];HPO:probinson[2013-01-07]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0000988	PMID:18710388	PCS		5/14			P	HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001873	PMID:16582076	PCS		6/7			P	HPO:probinson[2013-01-07]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0000952	PMID:18710388	PCS		8/14			P	HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001744	PMID:18710388;PMID:16582076	PCS		21/21			P	HPO:probinson[2013-01-07];HPO:probinson[2020-10-13]
OMIM:603552	Hemophagocytic lymphohistiocytosis, familial, 4		HP:0001875	PMID:16582076	PCS		5/7			P	HPO:probinson[2013-01-07]
OMIM:613027	Glycogen storage disease IXc		HP:0003621	PMID:9384616	PCS		1/2			C	HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0002155	PMID:9384616;PMID:8896567	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:6000333	PMID:21634085	PCS					P	HPO:probinson[2024-02-27]
OMIM:613027	Glycogen storage disease IXc		HP:0001252	PMID:8896567	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0002151	PMID:9384616	PCS		1/2			P	HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0001394	PMID:9384616	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0002240	PMID:8896567	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0003593	PMID:8896567	PCS		3/3			C	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0003162	PMID:8896567	PCS		1/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0001270	PMID:8896567	PCS		2/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0001408	PMID:8896567	PCS		1/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0011463	PMID:9384616	IEA		1/2			C	HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0000007	PMID:8896567	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0001943	PMID:9384616	PCS		1/2			P	HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0001946	OMIM:613027	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613027	Glycogen storage disease IXc		HP:0008897	PMID:9384616	PCS		1/2			P	HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0001510	PMID:8896567	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0002910	PMID:9384616;PMID:8896567	PCS		4/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0001744	OMIM:613027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613027	Glycogen storage disease IXc		HP:0006568	PMID:9384616	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:613027	Glycogen storage disease IXc		HP:0003128	OMIM:613027	IEA					P	HPO:skoehler[2010-06-19]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0003577	PMID:22512483	PCS		1/3			C	HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000100	PMID:22512483	PCS	HP:0003577	3/3			P	HPO:probinson[2013-01-09]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0005972	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0001030	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000160	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000083	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0001252	OMIM:614748	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0003593	PMID:22512483	PCS		1/3			C	HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0003073	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0010783	OMIM:614748	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0045075	PMID:22512483	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0011220	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0001806	PMID:22512483	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000316	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0006530	PMID:22512483	PCS		2/3			P	HPO:probinson[2013-02-18]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000774	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000653	PMID:22512483	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000311	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0003623	PMID:22512483	PCS		1/3			C	HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0002213	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000252	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000771	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0002098	PMID:22512483	PCS	HP:0003577	3/3			P	HPO:probinson[2013-02-18]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000097	PMID:22512483	PCS	HP:0003577	3/3			P	HPO:probinson[2013-02-18]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000093	OMIM:614748	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000092	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0012213	OMIM:614748	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0008066	PMID:22512483	PCS		3/3			P	HPO:probinson[2013-02-18]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000448	OMIM:614748	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0002209	PMID:22512483	PCS		3/3			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000007	PMID:22512483	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0000400	OMIM:614748	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0008404	PMID:22512483	PCS		3/3			P	HPO:probinson[2013-02-18]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0002205	PMID:22512483	PCS		2/3			P	HPO:probinson[2013-02-18]
OMIM:614748	Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital		HP:0002643	OMIM:614748	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614990	Usher syndrome, type IK		HP:0003577	OMIM:614990	TAS					C	HPO:skoehler[2013-01-21]
OMIM:614990	Usher syndrome, type IK		HP:0001751	OMIM:614990	TAS					P	HPO:skoehler[2013-01-21]
OMIM:614990	Usher syndrome, type IK		HP:0000007	OMIM:614990	TAS					I	HPO:skoehler[2013-01-21]
OMIM:614990	Usher syndrome, type IK		HP:0001270	OMIM:614990	TAS					P	HPO:skoehler[2013-01-21]
OMIM:614990	Usher syndrome, type IK		HP:0000510	OMIM:614990	TAS					P	HPO:skoehler[2013-01-21]
OMIM:611630	Epilepsy, familial temporal lobe, 3		HP:0002384	PMID:17377072	PCS		8/11			P	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:611630	Epilepsy, familial temporal lobe, 3		HP:0007334	PMID:17377072	PCS		4/11			P	HPO:probinson[2021-06-26]
OMIM:611630	Epilepsy, familial temporal lobe, 3		HP:0012005	PMID:17377072	PCS		10/11			P	HPO:probinson[2012-07-21];HPO:probinson[2021-06-26]
OMIM:611630	Epilepsy, familial temporal lobe, 3		HP:0000006	PMID:17377072	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-06-26]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0008936	PMID:27427983	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0002972	PMID:27427983	PCS		3/3			P	HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0001531	PMID:27427983	PCS		4/4			P	HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0003212	PMID:27427983	PCS		1/3			P	HPO:probinson[2020-10-12];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0011968	PMID:27427983	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0000260	PMID:27427983	PCS	HP:0003577	2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0011946	PMID:27427983	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0003496	PMID:27427983	PCS		3/3			P	HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0011800	PMID:27427983	PCS		1/4			P	HPO:probinson[2020-10-12];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0031402	PMID:27427983	PCS					P	HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0005280	PMID:27427983	PCS		1/4			P	HPO:probinson[2020-10-12];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0011342	PMID:27427983	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0011133	PMID:27427983	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0001518	PMID:27427983	PCS	HP:0003577	1/4			P	HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0000778	PMID:27427983	PCS		3/3			P	HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0000316	PMID:27427983	PCS		1/4			P	HPO:probinson[2020-10-12];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0000007	PMID:27427983	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0000964	PMID:27427983	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0002514	PMID:27427983	PCS		2/2			P	HPO:probinson[2020-10-12];HPO:probinson[2020-10-12]
OMIM:617241	Lung disease, immunodeficiency, and chromosome breakage syndrome		HP:0005415	PMID:27427983	PCS		3/3			P	HPO:probinson[2020-10-12]
OMIM:233100	Renal glucosuria		HP:0001959	OMIM:233100	IEA					P	HPO:iea[2009-02-17]
OMIM:233100	Renal glucosuria		HP:0002591	OMIM:233100	IEA					P	HPO:iea[2009-02-17]
OMIM:233100	Renal glucosuria		HP:0003828	OMIM:233100	TAS					M	HPO:skoehler[2012-10-17]
OMIM:233100	Renal glucosuria		HP:0003076	OMIM:233100	IEA					P	HPO:iea[2009-02-17]
OMIM:233100	Renal glucosuria		HP:0000007	OMIM:233100	IEA					I	HPO:iea[2009-02-17]
OMIM:233100	Renal glucosuria		HP:0000103	OMIM:233100	IEA					P	HPO:iea[2009-02-17]
OMIM:233100	Renal glucosuria		HP:0000006	OMIM:233100	TAS					I	HPO:skoehler[2012-10-17]
OMIM:233100	Renal glucosuria		HP:0010677	OMIM:233100	TAS		HP:0040283			P	HPO:skoehler[2010-06-18]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0002750	OMIM:608361	IEA					P	HPO:iea[2009-02-17]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0002970	OMIM:608361	IEA					P	HPO:iea[2009-02-17]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0000926	OMIM:608361	IEA					P	HPO:iea[2009-02-17]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0003370	OMIM:608361	IEA					P	HPO:iea[2009-02-17]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0003508	OMIM:608361	IEA					P	HPO:iea[2009-02-17]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0002857	OMIM:608361	IEA					P	HPO:iea[2009-02-17]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0000006	OMIM:608361	IEA					I	HPO:iea[2009-02-17]
OMIM:608361	Spondyloepiphyseal dysplasia, Kimberley type		HP:0002655	OMIM:608361	IEA					P	HPO:iea[2009-02-17]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0000819	PMID:33164986	PCS		6/6			P	HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0002069	PMID:33164986	PCS	HP:0003593	6/6			P	HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0000252	PMID:33164986	PCS		6/6		HP:0012828	P	HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0006956	PMID:33164986	PCS		1/4			P	HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0001518	PMID:33164986	PCS	HP:0003577	6/6			P	HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0001263	PMID:33164986	PCS		5/6			P	HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0003593	PMID:33164986	PCS		6/6			C	HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0000007	PMID:33164986	PCS					I	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:619278	Microcephaly, epilepsy, and diabetes syndrome 2		HP:0040217	PMID:33164986	PCS		5/5			P	HPO:probinson[2021-05-31]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0002135	PMID:19248180	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000121	PMID:29663634	PCS					P	HPO:nvasilevsky[2018-08-02]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000110	OMIM:146255	IEA					P	HPO:iea[2009-02-17]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0003577	PMID:19248180	PCS		1/1			C	HPO:probinson[2022-08-17]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0008718	PMID:19248180	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000100	PMID:29663634	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-01-26]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0003762	PMID:17309062	PCS		HP:0040283	FEMALE		P	HPO:skoehler[2012-11-18];HP:probinson[2019-01-26]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000790	PMID:29663634	PCS					P	HPO:nvasilevsky[2018-08-02]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0001153	PMID:17309062	PCS		HP:0040283	FEMALE		P	HPO:skoehler[2012-11-18];HP:probinson[2019-01-26]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000151	PMID:21834031	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0003250	PMID:21834031	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000093	PMID:29663634	PCS					P	HPO:nvasilevsky[2018-08-02]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0001281	PMID:21834031	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0012622	PMID:29663634	PCS					P	HPO:probinson[2014-01-18];HP:probinson[2019-01-26]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000829	PMID:29663634;PMID:21834031;PMID:19248180	PCS		170/182			P	HPO:probinson[2021-07-08];HPO:iea[2009-02-17];HPO:nvasilevsky[2018-08-02];HP:probinson[2019-01-26]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0008341	PMID:29663634	PCS					P	HPO:nvasilevsky[2018-08-02];HPO:nvasilevsky[2018-08-02]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000407	PMID:29663634;PMID:21834031;PMID:19248180	PCS		176/182			P	HPO:probinson[2021-07-08];HPO:nvasilevsky[2018-08-02];HP:probinson[2019-01-26]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000508	PMID:19248180	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000538	PMID:19248180	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000006	PMID:29663634	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-01-26]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000666	PMID:19248180	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0002049	PMID:29663634	PCS					P	HPO:nvasilevsky[2018-08-02];HPO:nvasilevsky[2018-08-02]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0000786	PMID:21834031	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:146255	Hypoparathyroidism, sensorineural deafness, and renal dysplasia		HP:0004722	OMIM:146255	TAS					P	HPO:probinson[2014-01-18]
OMIM:100200	Abducens palsy		HP:0000486	OMIM:100200	IEA					P	HPO:iea[2009-02-17]
OMIM:100200	Abducens palsy		HP:0006897	OMIM:100200	IEA					P	HPO:iea[2009-02-17]
OMIM:100200	Abducens palsy		HP:0000006	OMIM:100200	IEA					I	HPO:iea[2009-02-17]
OMIM:617255	Lissencephaly 8		HP:0003236	PMID:27773428	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0002365	PMID:27773428	PCS		6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0001250	PMID:27773428	PCS	HP:0003593	6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0002085	PMID:27773428	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0003593	PMID:27773428	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0006808	PMID:27773428	PCS		1/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0010862	PMID:27773428	PCS		9/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0031882	PMID:27773428	PCS		4/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0007260	PMID:27773428	PCS		7/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0000518	PMID:27773428	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0002119	PMID:27773428	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0006951	PMID:27773428	PCS		1/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0001249	PMID:27773428	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0008936	PMID:27773428	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0003202	PMID:27773428	PCS		0/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0000252	PMID:27773428	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0001344	PMID:27773428	PCS		2/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0001762	PMID:27773428	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0000750	PMID:27773428	PCS		9/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0031936	PMID:27773428	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0002079	PMID:27773428	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0001321	PMID:27773428	PCS		3/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0001263	PMID:27773428	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0002194	PMID:27773428	PCS		9/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0012434	PMID:27773428	PCS		9/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0034353	PMID:27773428	PCS		9/9			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0000729	PMID:27773428	PCS		2/5			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0000007	PMID:27773428	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0000568	PMID:27773428	PCS		1/8			P	HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0000648	PMID:27773428	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617255	Lissencephaly 8		HP:0002126	PMID:27773428	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0002751	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0003301	OMIM:184100	TAS					P	HPO:skoehler[2014-09-21]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0005743	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0001552	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0003311	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0000272	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0000470	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0030839	OMIM:184100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0030838	OMIM:184100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0000926	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0002938	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0000768	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0003308	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0000006	OMIM:184100	IEA					I	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0008922	OMIM:184100	IEA					P	HPO:iea[2009-02-17]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0001369	OMIM:184100	TAS					P	HPO:skoehler[2014-09-21]
OMIM:184100	Spondyloepiphyseal dysplasia tarda, autosomal dominant		HP:0002655	OMIM:184100	TAS					P	HPO:skoehler[2015-01-21]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000365	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002023	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000243	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0003196	PMID:25804025;PMID:16158429	PCS		2/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0012471	PMID:16158429	PCS		4/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0009101	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000998	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000238	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000879	PMID:16158429	PCS		1/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002898	OMIM:312870	TAS					P	HPO:skoehler[2017-07-13]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001169	OMIM:312870	TAS					P	HPO:probinson[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0008416	PMID:16158429	PCS		2/6			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000891	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000098	OMIM:312870	TAS					P	HPO:skoehler[2017-07-13]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000494	PMID:25804025	PCS		1/1			P	HPO:iea[2017-05-25];HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0100259	OMIM:312870	TAS					P	HPO:skoehler[2017-07-13]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000767	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0008523	PMID:17223397	PCS					P	HPO:probinson[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000768	PMID:16158429	PCS		1/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0003517	PMID:17603795	PCS	HP:0003577	5/7			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002667	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000126	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002245	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002884	PMID:16158429	PCS		1/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000189	PMID:16158429	PCS		3/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000463	PMID:25804025;PMID:16158429	PCS		2/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001274	PMID:16158429	PCS		1/6			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002240	PMID:25804025;PMID:16158429	PCS		2/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001270	PMID:16158429;PMID:17603795	PCS		8/13			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0006176	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001669	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001548	PMID:17603795	IEA		4/7			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000337	PMID:16158429	PCS		5/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0006610	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000212	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001667	PMID:16158429	PCS		1/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001320	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001561	PMID:16158429	PCS	HP:0011461	2/2			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0004279	PMID:16158429	PCS		1/6			P	HPO:probinson[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002650	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000750	PMID:17603795	PCS		5/7			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001162	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0003185	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001837	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000107	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001799	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002643	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000105	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000286	PMID:16158429	PCS		2/6			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001773	OMIM:312870	TAS					P	HPO:probinson[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002101	OMIM:312870	TAS					P	HPO:probinson[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001252	PMID:16158429	PCS		2/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000280	PMID:25804025;PMID:16158429	PCS		6/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0009381	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000316	PMID:25804025;PMID:16158429	PCS		5/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001769	OMIM:312870	TAS					P	HPO:probinson[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001643	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000158	PMID:16158429;PMID:17603795	PCS		11/13			P	HPO:probinson[2021-11-24];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001642	PMID:25804025	PCS		1/1			P	HPO:iea[2017-05-25];HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000297	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001540	PMID:16158429	PCS		2/6			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000175	PMID:25804025	PCS		1/1			P	HPO:iea[2017-05-25];HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0005580	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001419	PMID:8589713	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0011330	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001537	PMID:25804025;PMID:17603795	PCS		2/8			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002869	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000689	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0005616	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000047	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000384	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0004467	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000023	PMID:17603795	PCS		1/7			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001233	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0004464	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0003375	OMIM:312870	TAS					P	HPO:probinson[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0011675	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001629	PMID:25804025	PCS		1/1			P	HPO:iea[2017-05-25];HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0009882	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001748	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002711	PMID:16158429	PCS		4/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002558	PMID:25804025;PMID:16158429	PCS		5/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000773	PMID:16158429	PCS		2/6			P	HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000256	PMID:25804025;PMID:16158429	PCS		2/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001744	PMID:16158429	PCS		1/6			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000776	PMID:17603795	PCS		2/7			P	HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000154	PMID:25804025;PMID:16158429	PCS		5/7			P	HPO:probinson[2022-02-01];HPO:iea[2017-05-25];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0003422	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000431	PMID:25804025	PCS		1/1			P	HPO:probinson[2017-05-25];HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001762	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0004510	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0009908	PMID:25804025;PMID:16158429	PCS		4/7			P	HPO:probinson[2022-02-01];HPO:probinson[2021-11-24]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0005160	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0005280	PMID:25804025	PCS		1/1			P	HPO:skoehler[2017-05-25];HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0011304	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001638	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0001631	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000303	PMID:25804025	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0002566	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:312870	Simpson-Golabi-Behmel syndrome, type 1		HP:0000028	OMIM:312870	IEA					P	HPO:iea[2017-05-25]
OMIM:153880	Macular edema, cystoid		HP:0000486	OMIM:153880	IEA					P	HPO:iea[2009-02-17]
OMIM:153880	Macular edema, cystoid		HP:0007947	OMIM:153880	IEA					P	HPO:iea[2009-02-17]
OMIM:153880	Macular edema, cystoid		HP:0000540	OMIM:153880	IEA					P	HPO:skoehler[2010-06-20]
OMIM:153880	Macular edema, cystoid		HP:0000969	OMIM:153880	IEA					P	HPO:skoehler[2010-06-20]
OMIM:153880	Macular edema, cystoid		HP:0011505	OMIM:153880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:153880	Macular edema, cystoid		HP:0007754	OMIM:153880	TAS					P	HPO:skoehler[2015-01-21]
OMIM:153880	Macular edema, cystoid		HP:0000006	OMIM:153880	IEA					I	HPO:iea[2009-02-17]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003015	OMIM:603546	TAS					P	HPO:probinson[2012-05-26]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0001374	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0001498	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0004322	PMID:22152677	PCS		7/8			P	HPO:probinson[2013-04-12];HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0001252	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003370	OMIM:603546	TAS					P	HPO:probinson[2012-05-26]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0001290	OMIM:603546	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0010301	OMIM:603546	IEA					P	HPO:skoehler[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003071	OMIM:603546	TAS					P	HPO:probinson[2012-06-18]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0010585	OMIM:603546	TAS					P	HPO:probinson[2012-06-18]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0100531	PMID:22152677	PCS		1/8			P	HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0005092	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003090	OMIM:603546	TAS					P	HPO:probinson[2012-05-26]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0012297	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0012299	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0012296	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0008457	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0006454	OMIM:603546	TAS				HP:0012828	P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0002857	PMID:22152677	PCS		4/8			P	HPO:probinson[2013-04-12];HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0000977	OMIM:603546	TAS					P	HPO:skoehler[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0006016	OMIM:603546	TAS				HP:0012828	P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0008755	PMID:22152677	PCS		5/8			P	HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0005008	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003301	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003048	PMID:22152677	PCS		6/8			P	HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0002650	OMIM:603546;PMID:22152677	PCS		13/18			P	HPO:probinson[2024-03-10];HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003025	OMIM:603546	TAS					P	HPO:probinson[2012-05-26]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0002651	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0002970	PMID:22152677	PCS		2/8			P	HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0001382	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0008819	OMIM:603546	TAS					P	HPO:skoehler[2013-05-31]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0000272	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0005121	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0011800	PMID:22152677	PCS		8/8			P	HPO:skoehler[2013-11-28];HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0003083	OMIM:603546	IEA					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0002808	PMID:22152677	PCS		3/8			P	HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0010582	PMID:12966527	PCS					P	HPO:probinson[2012-06-18]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0002827	PMID:22152677	PCS		1/8			P	HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0006127	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0000006	PMID:22152677	PCS					I	HPO:probinson[2013-04-12];HPO:probinson[2024-03-10]
OMIM:603546	Spondyloepimetaphyseal dysplasia with joint laxity, type 2		HP:0009836	OMIM:603546	TAS					P	HPO:probinson[2013-04-12]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000486	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000482	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000639	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000627	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000519	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0011483	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000558	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0007750	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0007663	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000568	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000659	OMIM:604229	TAS					P	HPO:skoehler[2015-01-27]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0007676	OMIM:604229	TAS					P	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000647	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000006	PMID:10441571	PCS					I	HPO:probinson[2020-07-19]
OMIM:604229	Anterior segment dysgenesis 5, multiple subtypes		HP:0000501	OMIM:604229	TAS					P	HPO:probinson[2020-07-19]
OMIM:149600	Labia minora, incomplete adhesion of		HP:0000119	OMIM:149600	IEA					P	HPO:iea[2009-02-17]
OMIM:149600	Labia minora, incomplete adhesion of		HP:0000006	OMIM:149600	IEA					I	HPO:iea[2009-02-17]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001276	PMID:32738225	PCS		1/17			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0003577	PMID:32738225	PCS		6/24			C	HPO:probinson[2022-03-17]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0002188	PMID:32738225	PCS		2/10			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001371	PMID:32738225	PCS		1/22			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0003593	PMID:32738225	PCS		18/24			C	HPO:probinson[2020-12-22];HPO:probinson[2022-03-17]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0032794	PMID:32738225	PCS		1/24			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001290	PMID:32738225	PCS		7/17			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0012430	PMID:32738225	PCS		1/10			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0100702	PMID:32738225	PCS		1/10			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0025336	PMID:32738225	PCS		10/14			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0030084	PMID:32738225	PCS		3/22			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001302	PMID:32738225	PCS		1/10			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001249	PMID:32738225	PCS		24/24			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001347	PMID:32738225	PCS		1/15			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001265	PMID:32738225	PCS		10/15			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0000252	PMID:32738225	PCS		24/24			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0000750	PMID:32738225	PCS		22/24			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0002650	PMID:32738225	PCS		1/22			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0031936	PMID:32738225	PCS		19/19			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0002079	PMID:32738225	PCS		1/10			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001263	PMID:32738225	PCS		24/24			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0010830	PMID:32738225	PCS		5/12			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0025190	PMID:32738225	PCS		14/24			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0009830	PMID:32738225	PCS		5/17			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0000007	PMID:32738225	PCS					I	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0000601	PMID:32738225	PCS		1/22			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0001159	PMID:32738225	PCS		1/22			P	HPO:probinson[2020-12-22]
OMIM:619091	Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive		HP:0007359	PMID:32738225	PCS		2/24			P	HPO:probinson[2020-12-22]
OMIM:182940	Neural tube defects, susceptibility to		HP:0001012	OMIM:182940	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182940	Neural tube defects, susceptibility to		HP:0002323	OMIM:182940	IEA					P	HPO:iea[2009-02-17]
OMIM:182940	Neural tube defects, susceptibility to		HP:0008482	OMIM:182940	IEA					P	HPO:iea[2009-02-17]
OMIM:182940	Neural tube defects, susceptibility to		HP:0002475	OMIM:182940	TAS	HP:0003577				P	HPO:skoehler[2012-10-17]
OMIM:182940	Neural tube defects, susceptibility to		HP:0003298	OMIM:182940	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:182940	Neural tube defects, susceptibility to		HP:0000020	OMIM:182940	IEA					P	HPO:iea[2009-02-17]
OMIM:182940	Neural tube defects, susceptibility to		HP:0012032	OMIM:182940	IEA					P	HPO:skoehler[2018-10-08]
OMIM:182940	Neural tube defects, susceptibility to		HP:0000238	OMIM:182940	IEA					P	HPO:iea[2009-02-17]
OMIM:182940	Neural tube defects, susceptibility to		HP:0010305	OMIM:182940	IEA					P	HPO:skoehler[2018-10-08]
OMIM:182940	Neural tube defects, susceptibility to		HP:0000960	OMIM:182940	IEA					P	HPO:skoehler[2019-09-07]
OMIM:182940	Neural tube defects, susceptibility to		HP:0000006	OMIM:182940	TAS					I	HPO:skoehler[2013-05-29]
OMIM:620610	Oocyte/zygote/embryo maturation arrest 21		HP:0008222	PMID:33948904;PMID:33953335	PCS		11/11			P	HPO:probinson[2024-03-12]
OMIM:620610	Oocyte/zygote/embryo maturation arrest 21		HP:0011462	PMID:33953335	PCS		7/7			C	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620610	Oocyte/zygote/embryo maturation arrest 21		HP:0033336	PMID:33948904	PCS		2/2			P	HPO:probinson[2024-03-12]
OMIM:620610	Oocyte/zygote/embryo maturation arrest 21		HP:0000006	PMID:33953335	PCS					I	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002421	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000483	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001212	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000486	PMID:24531329	PCS		1/10			P	HPO:skoehler[2015-05-31]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0004322	PMID:24531329	PCS		2/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0003196	PMID:29724491;PMID:24531329	PCS		32/73			P	HPO:probinson[2023-02-11];HPO:skoehler[2014-08-24];HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002020	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0003593	PMID:24531329	PCS		3/10			C	HPO:skoehler[2015-12-30]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0012745	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0010442	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0008093	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0010055	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0010296	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000752	PMID:28221363	PCS					P	HPO:skoehler[2014-08-24];HP:probinson[2018-10-13]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002019	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000358	PMID:29724491;PMID:24531329	PCS		11/78			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0003623	PMID:24531329	PCS		5/10			C	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0003763	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000494	PMID:29724491;PMID:24531329	PCS		23/70			P	HPO:probinson[2023-02-11];HPO:skoehler[2014-08-24];HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000010	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001344	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0011800	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001182	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0010677	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000767	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002705	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0004209	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001852	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000006	PMID:24531329	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000369	PMID:29724491;PMID:24531329	PCS		11/78			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002028	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0003577	PMID:24531329	PCS		1/10			C	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000582	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000343	PMID:29724491	PCS		22/56			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000463	PMID:29724491	PCS		28/60			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001270	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000737	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000739	PMID:24531329	PCS		3/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000733	PMID:24531329	PCS		2/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000219	PMID:29724491;PMID:24531329	PCS		49/74			P	HPO:probinson[2023-02-11];HPO:skoehler[2014-08-24];HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002119	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000455	PMID:29724491	PCS		15/57			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000179	PMID:29724491	PCS		20/55			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001788	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002015	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0003621	PMID:24531329	PCS		1/10			C	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0006956	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002650	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000233	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000232	PMID:29724491	PCS		25/55			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0012683	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0032792	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000508	PMID:24531329	PCS		1/10			P	HPO:skoehler[2015-05-31]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0007651	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0006288	PMID:28221363	PCS		44/54			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000505	OMIM:615873	TAS					P	HPO:skoehler[2015-05-31]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000625	PMID:29724491	PCS		12/63			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001956	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0007018	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000105	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000286	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0010529	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001250	PMID:24531329	PCS		1/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001252	PMID:24531329	PCS		6/10			P	HPO:skoehler[2014-11-26]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000283	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000280	PMID:29724491	PCS		11/65			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000319	OMIM:615873	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0011220	PMID:29724491;PMID:24531329	PCS		45/74			P	HPO:probinson[2023-02-11];HPO:skoehler[2014-08-24];HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000717	PMID:24531329	PCS		5/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000316	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0003307	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002857	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001488	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001763	PMID:24531329	PCS		3/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001249	OMIM:615873	IEA		10/10			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000677	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0030148	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000331	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0011968	PMID:24531329	PCS		2/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001382	PMID:24531329	PCS		3/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001263	PMID:24531329	PCS		4/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000691	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002591	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0011327	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0009890	PMID:29724491	PCS		33/66			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0012420	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000729	PMID:24531329	PCS		3/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0006385	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000722	PMID:24531329	PCS		1/10			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001653	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000963	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000687	PMID:29724491;PMID:24531329	PCS		19/62			P	HP:probinson[2019-01-27];HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0010628	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000540	PMID:24531329	PCS		2/10			P	HPO:skoehler[2015-05-31]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0040082	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001508	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000817	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0030680	OMIM:615873	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001627	OMIM:615873	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000378	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000154	PMID:29724491;PMID:24531329	PCS		14/66			P	HP:probinson[2019-01-27];HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000670	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000431	PMID:29724491;PMID:24531329	PCS		34/76			P	HPO:probinson[2023-02-11];HPO:skoehler[2014-08-24];HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000276	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002572	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002171	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0045025	PMID:29724491	PCS		14/58			P	HP:probinson[2019-01-27]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0011147	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0012760	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000824	PMID:29724491	PCS		5/46			P	HPO:probinson[2018-10-07]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001511	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0002205	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0200055	OMIM:615873	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001631	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0000028	PMID:24531329	PCS		1/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001634	PMID:24531329	PCS		2/10			P	HPO:probinson[2023-02-11]
OMIM:615873	Helsmoortel-van der Aa syndrome		HP:0001513	PMID:24531329	PCS		1/10			P	HPO:skoehler[2014-08-24]
OMIM:250100	Metachromatic leukodystrophy		HP:0001332	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001250	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0000020	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001252	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001251	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001290	OMIM:250100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:250100	Metachromatic leukodystrophy		HP:0000738	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0005609	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0000712	OMIM:250100	PCS					P	HPO:probinson[2012-04-11]
OMIM:250100	Metachromatic leukodystrophy		HP:0001268	OMIM:250100	PCS					P	HPO:probinson[2012-04-11]
OMIM:250100	Metachromatic leukodystrophy		HP:0001249	OMIM:250100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001347	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001265	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0003445	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0002510	OMIM:250100	PCS					P	HPO:probinson[2012-04-11]
OMIM:250100	Metachromatic leukodystrophy		HP:0001288	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0003487	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001283	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0001260	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0002371	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0002072	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0034687	PMID:6137805	PCS					P	HPO:probinson[2023-03-31]
OMIM:250100	Metachromatic leukodystrophy		HP:0034863	OMIM:250100	TAS					P	HPO:probinson[2023-07-18]
OMIM:250100	Metachromatic leukodystrophy		HP:0001082	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0011096	OMIM:250100	PCS					P	HPO:probinson[2012-04-11]
OMIM:250100	Metachromatic leukodystrophy		HP:0007133	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0000007	OMIM:250100	IEA					I	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0000648	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0002922	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0000746	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0000762	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0002500	OMIM:250100	IEA					P	HPO:iea[2009-02-17]
OMIM:250100	Metachromatic leukodystrophy		HP:0002445	OMIM:250100	TAS					P	HPO:skoehler[2013-01-22]
OMIM:219500	CYSTATHIONINURIA		HP:0003153	OMIM:219500	TAS					P	HPO:probinson[2009-02-17]
OMIM:219500	CYSTATHIONINURIA		HP:0000007	OMIM:219500	TAS					I	HPO:probinson[2009-02-17]
OMIM:254400	Mycosis fungoides		HP:0008069	OMIM:254400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254400	Mycosis fungoides		HP:0000964	OMIM:254400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254400	Mycosis fungoides		HP:0002716	OMIM:254400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254400	Mycosis fungoides		HP:0000989	OMIM:254400	IEA					P	HPO:iea[2009-02-17]
OMIM:254400	Mycosis fungoides		HP:0200035	OMIM:254400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254400	Mycosis fungoides		HP:0010783	OMIM:254400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254400	Mycosis fungoides		HP:0002665	OMIM:254400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254400	Mycosis fungoides		HP:0003765	OMIM:254400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0003676	PMID:29395073	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001332	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001310	PMID:29395073	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001272	PMID:29395073	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001252	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0003593	PMID:29395073	PCS		2/2			C	HPO:probinson[2023-03-01];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001251	PMID:29395073	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0002061	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001270	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0033643	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0000639	PMID:29395073	PCS		1/2			P	HPO:skoehler[2019-04-18]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0002415	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001348	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0008936	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0002015	PMID:29395073	PCS		1/2			P	HPO:skoehler[2019-04-18]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0002059	PMID:29395073	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0000750	PMID:29395073	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001761	PMID:29395073	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0002079	PMID:29395073	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001260	PMID:29395073	PCS		1/2			P	HPO:skoehler[2018-10-08]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0012675	PMID:29395073	PCS		2/2			P	HPO:probinson[2023-03-01];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0000007	PMID:29395073	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0002505	PMID:29395073	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0000763	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0002503	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:617916	Neurodegeneration with brain iron accumulation 7		HP:0001337	PMID:29395073	PCS		1/2			P	HPO:probinson[2023-03-01]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001254	PMID:12410208	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0003236	PMID:12410208	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001250	OMIM:608836;PMID:12410208	PCS		11/12			P	HPO:iea[2009-02-17];HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0011936	OMIM:608836	TAS					P	HPO:probinson[2012-06-10]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000083	PMID:12410208	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001252	PMID:12410208	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0008293	PMID:12410208	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000518	OMIM:608836	TAS					P	HPO:probinson[2013-04-09]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0011220	OMIM:608836	PCS					P	HPO:probinson[2012-03-18]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0011461	PMID:12410208	PCS		1/1			C	HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001800	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0100807	OMIM:608836	TAS					P	HPO:probinson[2013-04-09]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001522	PMID:12410208	PCS		1/1			C	HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000113	OMIM:608836	TAS	HP:0003577				P	HPO:probinson[2014-01-18]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0006799	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001403	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000358	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001644	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0031956	PMID:12410208	PCS		3/3			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000252	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0010511	OMIM:608836	TAS					P	HPO:skoehler[2013-08-10]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001182	OMIM:608836	TAS					P	HPO:probinson[2013-04-09]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0006380	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0009058	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000007	OMIM:608836	IEA					I	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002987	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002269	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002104	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000369	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000126	PMID:12410208	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0003455	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000340	OMIM:608836	TAS					P	HPO:probinson[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000189	OMIM:608836	TAS					P	HPO:skoehler[2013-08-18]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0003573	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001274	PMID:11477613	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002240	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0011675	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0031964	PMID:12410208	PCS		3/3			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0032066	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0007023	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000414	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0008872	PMID:12410208	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001987	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001943	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002878	OMIM:608836	TAS					P	HPO:skoehler[2014-06-24]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002119	PMID:11477613	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001945	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000218	PMID:11477613	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001742	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0006610	OMIM:608836	TAS					P	HPO:probinson[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0008315	PMID:12410208	PCS		1/1			P	HPO:probinson[2012-06-10];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002910	PMID:11389301	PCS					P	HPO:probinson[2012-03-18]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0007229	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001760	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002014	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0006559	PMID:12410208	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001562	OMIM:608836	PCS		HP:0040283			P	HPO:probinson[2012-03-18]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000396	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000110	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0011309	OMIM:608836	TAS					P	HPO:skoehler[2013-08-10]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001640	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002013	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000073	OMIM:608836	TAS					P	HPO:probinson[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002093	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001958	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0006561	PMID:12410208	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000348	OMIM:608836	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0001319	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0000105	PMID:11477613	PCS	HP:0003577	1/1			P	HPO:probinson[2014-01-18];HPO:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002643	PMID:12410208	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0002126	OMIM:608836	IEA					P	HPO:iea[2009-02-17]
OMIM:608836	Carnitine palmitoyltransferase II deficiency, lethal neonatal		HP:0003259	PMID:12410208	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0007957	OMIM:163200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0004322	OMIM:163200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001596	OMIM:163200	TAS					P	HPO:skoehler[2012-11-21]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001250	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001010	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0000085	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0000938	OMIM:163200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001548	OMIM:163200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0002757	OMIM:163200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0003109	OMIM:163200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001528	OMIM:163200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0003745	OMIM:163200	IEA					I	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0004912	OMIM:163200	TAS					P	HPO:skoehler[2010-06-20]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001249	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0007206	OMIM:163200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001028	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0002751	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0010815	OMIM:163200	TAS					P	HPO:skoehler[2012-11-21]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0003764	OMIM:163200	TAS					P	HPO:skoehler[2012-11-21]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001442	OMIM:163200	TAS					I	HPO:skoehler[2012-10-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001167	OMIM:163200	TAS					P	HPO:probinson[2014-05-24]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0002671	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001780	OMIM:163200	TAS					P	HPO:probinson[2014-05-24]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001680	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0010817	OMIM:163200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0011073	OMIM:163200	TAS					P	HPO:skoehler[2014-05-24]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0008064	OMIM:163200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0000826	OMIM:163200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0006482	OMIM:163200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0000602	OMIM:163200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0000267	OMIM:163200	IEA					P	HPO:iea[2009-02-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0001510	OMIM:163200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:163200	Schimmelpenning-Feuerstein-Mims syndrome		HP:0000589	OMIM:163200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0002982	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0007957	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0001773	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000684	PMID:26279204	PCS		1/4			P	HPO:iea[2009-02-17]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0003196	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0012785	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0011463	PMID:26279204	PCS		3/4			C	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000316	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0006951	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000278	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0007922	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000891	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0004334	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0002750	PMID:26279204	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0001263	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0011800	OMIM:601812	TAS					P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0100578	OMIM:601812	TAS					P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0034392	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0010562	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000407	PMID:26279204	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000327	OMIM:601812	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0200036	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000568	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000601	PMID:26279204	PCS		2/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000444	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000883	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000520	PMID:26279204	PCS		1/4			P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0001015	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000963	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000006	PMID:26279204	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000962	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0003577	PMID:26279204	PCS		1/4			C	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0009839	PMID:26279204	PCS		4/4			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000540	PMID:26279204	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0001156	PMID:26279204	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000460	OMIM:601812	TAS					P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0010500	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0001072	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0008070	PMID:26279204	PCS		1/4			P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0010941	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000939	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0001508	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0009882	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0100702	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0002757	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000972	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000256	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0011829	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000233	OMIM:601812	TAS					P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0010539	OMIM:601812	TAS					P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0004279	PMID:26279204	PCS		2/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0002650	PMID:26279204	PCS		1/4			P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0003100	PMID:26279204	PCS		1/4			P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000270	OMIM:601812	TAS					P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0007291	PMID:26279204	PCS		2/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0012040	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0007495	PMID:26279204	PCS		4/4			P	HPO:probinson[2023-02-28];HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000426	OMIM:601812	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0002925	OMIM:601812	IEA					P	HPO:iea[2009-02-17]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0002645	PMID:26279204	PCS		1/4			P	HPO:skoehler[2015-10-16]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0002007	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000586	PMID:26279204	PCS		1/4			P	HPO:probinson[2023-02-28]
OMIM:601812	Premature aging syndrome, Penttinen type		HP:0000347	PMID:26279204	PCS		1/4			P	HPO:skoehler[2015-10-16]
OMIM:615697	Epilepsy, familial temporal lobe, 6		HP:0002133	PMID:24021842	PCS		2/11			P	HPO:probinson[2021-06-26]
OMIM:615697	Epilepsy, familial temporal lobe, 6		HP:0002373	PMID:24021842	PCS		4/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-06-26]
OMIM:615697	Epilepsy, familial temporal lobe, 6		HP:0002384	PMID:24021842	PCS		5/11			P	HPO:probinson[2021-06-26]
OMIM:615697	Epilepsy, familial temporal lobe, 6		HP:0007334	PMID:24021842	PCS		4/11			P	HPO:probinson[2021-06-26]
OMIM:615697	Epilepsy, familial temporal lobe, 6		HP:0002349	PMID:24021842	PCS		4/11			P	HPO:probinson[2021-06-26]
OMIM:615697	Epilepsy, familial temporal lobe, 6		HP:0000006	PMID:24021842	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-26]
OMIM:166350	Osseous heteroplasia, progressive		HP:0003621	PMID:11784876	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:166350	Osseous heteroplasia, progressive		HP:0003676	PMID:11784876	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:166350	Osseous heteroplasia, progressive		HP:0009826	PMID:11784876	PCS					P	HPO:probinson[2023-01-17]
OMIM:166350	Osseous heteroplasia, progressive		HP:0025027	OMIM:166350	TAS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:166350	Osseous heteroplasia, progressive		HP:0003593	PMID:11784876	PCS					C	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-17]
OMIM:166350	Osseous heteroplasia, progressive		HP:0031013	PMID:11784876	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:166350	Osseous heteroplasia, progressive		HP:0011987	PMID:11784876	PCS					P	HPO:probinson[2023-01-17]
OMIM:166350	Osseous heteroplasia, progressive		HP:0000006	PMID:11784876	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0000453	OMIM:179270	IEA					P	HPO:iea[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0001245	OMIM:179270	TAS					P	HPO:probinson[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0000452	OMIM:179270	IEA					P	HPO:iea[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0009622	OMIM:179270	IEA					P	HPO:iea[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0000565	OMIM:179270	IEA					P	HPO:iea[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0005280	OMIM:179270	IEA					P	HPO:iea[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0009778	OMIM:179270	IEA					P	HPO:iea[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0000006	OMIM:179270	IEA					I	HPO:iea[2009-02-17]
OMIM:179270	Radial ray hypoplasia with choanal atresia		HP:0002984	OMIM:179270	TAS					P	HPO:iea[2009-02-17]
OMIM:617080	Seizures, benign familial infantile, 5		HP:0002069	PMID:26677014	PCS		15/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-11]
OMIM:617080	Seizures, benign familial infantile, 5		HP:0002384	PMID:26677014	PCS		3/16			P	HPO:probinson[2023-04-11]
OMIM:617080	Seizures, benign familial infantile, 5		HP:0011463	PMID:26677014	PCS		8/16			C	HPO:probinson[2023-04-11]
OMIM:617080	Seizures, benign familial infantile, 5		HP:0007166	PMID:26677014	PCS		5/16			P	HPO:probinson[2023-04-11]
OMIM:617080	Seizures, benign familial infantile, 5		HP:0003593	PMID:26677014	PCS		8/16			C	HPO:probinson[2023-04-11]
OMIM:617080	Seizures, benign familial infantile, 5		HP:0000006	PMID:26677014	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-11]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002421	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002069	PMID:35314505	PCS		4/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002521	PMID:35314505	PCS		1/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002188	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002384	PMID:35314505	PCS		3/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002121	PMID:35314505	PCS		4/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0001252	PMID:35314505;PMID:34448338	PCS		2/9			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0003593	PMID:35314505	PCS		8/8			C	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0001251	PMID:35314505	PCS		2/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0032794	PMID:35314505	PCS		7/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002381	PMID:35314505	PCS		1/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0031491	PMID:35314505	PCS		2/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0100702	PMID:35314505	PCS		1/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0000752	PMID:35314505	PCS		1/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0000256	PMID:35314505	PCS		1/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0001249	PMID:35314505	PCS		8/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0003623	PMID:31972370;PMID:34448338	PCS		2/2			C	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002179	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002510	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0000211	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0001344	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0025097	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0011968	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0010819	PMID:35314505	PCS		1/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0010851	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002392	PMID:35314505	PCS		3/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0011344	PMID:34448338	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0011097	PMID:31972370;PMID:34448338	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0032670	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0032792	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0000729	PMID:35314505	PCS		2/8			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0200134	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0002307	PMID:31972370	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619913	Developmental and epileptic encephalopathy 103		HP:0000006	PMID:31972370	PCS					I	HPO:probinson[2022-08-14]
OMIM:191900	Muckle-Wells syndrome		HP:0030953	PMID:25766347	PCS		2/2		HP:0025303	P	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0000365	PMID:14872505	PCS	HP:0011463	3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0004322	PMID:14872505	PCS		3/3			P	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0000083	PMID:9704852	PCS	HP:0003584				P	HPO:iea[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0003593	PMID:27435956	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:191900	Muckle-Wells syndrome		HP:0031191	PMID:27435956	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:191900	Muckle-Wells syndrome		HP:0012432	PMID:14872505	PCS		3/3			P	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0011463	PMID:25766347	PCS					C	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0002516	PMID:27435956	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:191900	Muckle-Wells syndrome		HP:0002315	PMID:27435956	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:191900	Muckle-Wells syndrome		HP:0003326	OMIM:191900	TAS				HP:0025303	P	HPO:probinson[2009-02-17]
OMIM:191900	Muckle-Wells syndrome		HP:0002633	PMID:27435956	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:191900	Muckle-Wells syndrome		HP:0003565	PMID:25766347;PMID:27435956	PCS		3/3		HP:0025303	P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:probinson[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0003621	PMID:25766347	PCS		1/2			C	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0005764	PMID:25766347	PCS		2/2		HP:0025303	P	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0001025	PMID:27435956	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:191900	Muckle-Wells syndrome		HP:0001085	PMID:27435956	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:191900	Muckle-Wells syndrome		HP:0011107	OMIM:191900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:191900	Muckle-Wells syndrome		HP:0011227	PMID:25766347;PMID:27435956	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0002829	PMID:14872505	PCS		3/3		HP:0025206;HP:0025303	P	HPO:probinson[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0000408	PMID:25766347	PCS	HP:0011462	2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0100759	PMID:25766347	PCS		2/2			P	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0040186	PMID:25766347;PMID:14872505	PCS		5/5		HP:0025303	P	HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0000509	PMID:14872505;PMID:27435956	PCS		3/4		HP:0025206;HP:0025303	P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:probinson[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0001917	PMID:9704852	PCS	HP:0003584				P	HPO:probinson[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0001954	PMID:25766347;PMID:14872505	PCS		5/5		HP:0025206;HP:0025303	P	HPO:probinson[2020-11-17];HPO:iea[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0000006	PMID:11687797	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-17]
OMIM:191900	Muckle-Wells syndrome		HP:0001974	PMID:25766347;PMID:27435956	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:skoehler[2010-06-20];HPO:probinson[2020-11-17]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000594	PMID:25561690	PCS		11/11			P	HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000486	OMIM:602499	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0007906	OMIM:602499	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000482	PMID:25561690	PCS		11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000639	OMIM:602499	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0007663	OMIM:602499	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000612	PMID:25561690	PCS		11/11			P	HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0007401	OMIM:602499	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0007720	PMID:25561690	PCS		11/11			P	HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000545	PMID:25561690	PCS		11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000006	PMID:25561690	PCS					I	HPO:nvasilevsky[2019-03-12];HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000567	PMID:25561690	PCS		11/11			P	HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0007800	PMID:25561690	PCS		11/11			P	HPO:probinson[2023-05-19]
OMIM:602499	Macrophthalmia, colobomatous, with microcornea		HP:0000588	PMID:25561690	PCS		9/11			P	HPO:probinson[2023-05-19]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0001385	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0002650	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0001762	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0001156	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0004322	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0003370	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0010049	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0002829	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0031174	PMID:12525546	PCS		7/10			P	HPO:probinson[2018-03-05]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0000007	OMIM:226900	IEA					I	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0006376	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0002656	OMIM:226900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0008802	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:226900	Epiphyseal dysplasia, multiple, 4		HP:0002654	OMIM:226900	IEA					P	HPO:iea[2009-02-17]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0001531	PMID:22127713	PCS		2/2			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0200039	PMID:19494218	PCS	HP:0003623	9/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0200039	PMID:19494219	PCS	HP:0003623	1/1			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0200039	PMID:22127713	PCS	HP:0003623	2/2			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0200039	PMID:32819369	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002240	OMIM:612852	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0001270	PMID:22127713	PCS		2/2			P	HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0011897	PMID:32819369	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0000938	PMID:19494219	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0025116	PMID:19494218	PCS	HP:0011461	5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002797	PMID:22127713;PMID:19494219;PMID:19494218	PCS		11/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0001744	OMIM:612852	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0025615	PMID:22127713	PCS		2/2			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0003623	PMID:22127713;PMID:19494219;PMID:19494218	PCS		12/12			C	HPO:probinson[2020-11-27];HPO:probinson[2020-10-19]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002754	PMID:19494218	PCS		8/9			P	HPO:skoehler[2015-01-27];HPO:probinson[2020-10-19]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002754	PMID:22127713	PCS		2/2			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002754	PMID:32819369	PCS	HP:0003593	1/1			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0003565	PMID:22127713;PMID:32819369	PCS		3/3			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0001386	PMID:19494218	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002098	PMID:19494218	PCS	HP:0003623				P	HPO:skoehler[2012-11-18];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0025092	PMID:19494219;PMID:19494218	PCS		3/3			P	HPO:probinson[2020-11-27];HPO:skoehler[2017-07-13];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0011227	PMID:22127713;PMID:19494219;PMID:32819369	PCS		4/4			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0010280	OMIM:612852	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002829	PMID:19494218	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0040165	PMID:19494218	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-19]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0000904	PMID:19494219	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002949	PMID:19494218	PCS		4/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-19]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0000007	PMID:19494218	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0000988	PMID:32819369	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0002206	PMID:19494218	PCS		1/9			P	HPO:probinson[2020-11-27]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0000885	PMID:19494218	PCS		9/9			P	HPO:probinson[2020-10-19]
OMIM:612852	Interleukin 1 receptor antagonist deficiency		HP:0000962	PMID:19494218	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-27]
OMIM:611383	Usher syndrome, type IID		HP:0003577	PMID:17171570	PCS		2/2			C	HPO:probinson[2022-12-17]
OMIM:611383	Usher syndrome, type IID		HP:0000365	PMID:17171570	PCS	HP:0003577	2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2022-12-17]
OMIM:611383	Usher syndrome, type IID		HP:0001751	PMID:17171570	PCS		0/2			P	HPO:probinson[2013-04-01];HPO:probinson[2022-12-17]
OMIM:611383	Usher syndrome, type IID		HP:0000662	PMID:17171570	PCS	HP:0011462	2/2			P	HPO:probinson[2022-12-17]
OMIM:611383	Usher syndrome, type IID		HP:0000007	PMID:17171570	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-12-17]
OMIM:611383	Usher syndrome, type IID		HP:0000510	PMID:17171570	PCS		2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2022-12-17]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0003202	OMIM:615683	TAS					P	HPO:skoehler[2015-09-11]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0000252	PMID:24482476	PCS		2/4			P	HPO:probinson[2015-05-10]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0001762	OMIM:615683	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0001288	PMID:24482476	PCS					P	HPO:probinson[2015-05-10]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0001260	PMID:24482476	PCS					P	HPO:probinson[2015-05-10]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0000718	OMIM:615683	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0000519	OMIM:615683	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0000007	PMID:24482476	PCS					I	HPO:probinson[2015-05-10]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0000823	OMIM:615683	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0001258	PMID:24482476	PCS		4/4			P	HPO:probinson[2015-05-10]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0001257	PMID:24482476	PCS		4/4			P	HPO:probinson[2015-05-10]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0002500	PMID:24482476	PCS		2/2			P	HPO:probinson[2015-05-10]
OMIM:615683	Spastic paraplegia 64, autosomal recessive		HP:0001249	PMID:24482476	PCS					P	HPO:probinson[2015-05-10]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0002003	PMID:21594994	PCS		2/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000286	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000483	PMID:21594994	PCS		2/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000343	PMID:21594994	PCS		2/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000486	PMID:21594994	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000540	PMID:21594994	PCS		2/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001250	PMID:21594994	PCS		1/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001252	PMID:21594994	PCS		1/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000280	PMID:21594994	PCS		4/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0012368	PMID:21594994	PCS		2/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001629	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000316	PMID:21594994	PCS		2/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0100807	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000637	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0008897	PMID:21594994	PCS		3/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0002615	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0009765	OMIM:615668	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001643	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000158	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001249	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000358	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000154	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000396	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0045082	OMIM:615668	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000750	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000331	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0002373	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001263	PMID:21594994	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000470	PMID:21594994	PCS		2/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0010511	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001519	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0010880	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000508	PMID:21594994	PCS		3/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000448	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000505	PMID:21594994	PCS		3/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000565	OMIM:615668	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0002007	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001631	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000322	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000960	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000006	PMID:21594994	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0000347	PMID:21594994	PCS		1/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:615668	Chromosome 5q12 deletion syndrome		HP:0001655	PMID:21594994	PCS		1/4			P	HPO:probinson[2023-05-21]
OMIM:260000	Hyperoxaluria, primary, type II		HP:6000670	PMID:28569194	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0000121	PMID:10484776	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-08]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0012100	PMID:28569194	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0003159	PMID:28569194;PMID:10484776	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08];ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0000083	PMID:10484776	PCS		1/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-08]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0000790	OMIM:260000	TAS					P	HPO:skoehler[2015-01-04]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0008672	PMID:28569194;PMID:10484776	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08];ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0003593	PMID:28569194	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0000007	PMID:10484776	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0011280	PMID:28569194	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:260000	Hyperoxaluria, primary, type II		HP:6000638	PMID:10484776	PCS					P	HPO:probinson[2024-04-03]
OMIM:260000	Hyperoxaluria, primary, type II		HP:0001942	PMID:28569194	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-24]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000286	PMID:26260076	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001892	PMID:26260076	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0003236	PMID:26260076	PCS		3/9			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000122	PMID:26260076	PCS		1/6			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001250	PMID:26260076	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0003155	PMID:26260076	PCS		5/9			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001290	PMID:26260076	PCS		3/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0012301	PMID:26260076	PCS		8/9			P	HPO:skoehler[2013-04-18];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000958	PMID:26260076	PCS		1/5			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0004719	PMID:26260076	PCS		1/6			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000238	PMID:26260076	PCS		1/6			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000114	PMID:26260076	PCS		1/10			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001643	PMID:26260076	PCS	HP:0003623	2/4			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001522	PMID:26260076	PCS		6/10			C	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000278	PMID:26260076	PCS		1/10			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002536	PMID:26260076	PCS		1/6			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001249	PMID:26260076	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000252	PMID:26260076	PCS		7/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002037	PMID:26260076	PCS		1/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001385	PMID:26260076	PCS		1/7			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002079	PMID:26260076	PCS		1/6			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0025533	PMID:26260076	PCS		1/5			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001263	PMID:26260076	PCS		7/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0030948	PMID:26260076	PCS		3/9			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0011840	PMID:26260076	PCS		1/10			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0100259	PMID:26260076	PCS		2/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000007	PMID:26260076	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000648	PMID:26260076	PCS		1/6			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000966	PMID:26260076	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0000962	PMID:26260076	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002028	PMID:26260076	PCS		3/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0003577	PMID:26260076	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001396	PMID:26260076	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001272	PMID:26260076	PCS		1/9			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002240	PMID:26260076	PCS		5/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001394	PMID:26260076	PCS		2/9			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002040	PMID:26260076	PCS		1/9			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001629	PMID:26260076	PCS	HP:0003577	1/4			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002719	PMID:26260076	PCS		7/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001508	PMID:26260076	PCS		3/10			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0006297	PMID:26260076	PCS		1/3			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002119	PMID:26260076	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002910	PMID:26260076	PCS		9/9			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001744	PMID:26260076	PCS		7/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002059	PMID:26260076	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0002848	PMID:26260076	PCS		1/10			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001511	PMID:26260076	PCS	HP:0030674				P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001873	PMID:26260076	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001510	PMID:26260076	PCS		5/7			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001631	PMID:26260076	PCS	HP:0003577	3/4			P	HPO:probinson[2020-09-12]
OMIM:614576	Congenital disorder of glycosylation, type IIl		HP:0001876	PMID:26260076	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0003236	PMID:10430757	PCS		0/4			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-03]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0001640	PMID:10430757	PCS		2/4			P	HPO:probinson[2022-07-03]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0003581	PMID:10430757	PCS		2/2			C	HPO:probinson[2022-07-03]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0006673	PMID:10430757	PCS		2/4			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-03]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0001635	PMID:10430757	PCS		2/4			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-03]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0012664	PMID:10430757	PCS		2/4			P	HPO:probinson[2022-07-03]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0000006	PMID:10430757	PCS					I	HPO:probinson[2013-01-09]
OMIM:604765	Cardiomyopathy, dilated, 1I		HP:0001644	PMID:10430757	PCS		2/4			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-03]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0003621	PMID:20727754	PCS		4/5			C	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0002067	PMID:20727754	PCS		1/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0004322	PMID:20727754	PCS		1/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0030223	PMID:20727754	PCS		2/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0001260	PMID:20727754	PCS		2/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0001285	PMID:20727754	PCS		1/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0002064	PMID:20727754	PCS		1/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0032005	PMID:20727754	PCS		1/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0025162	PMID:20727754	PCS		1/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0007183	PMID:20727754	PCS		3/3			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0011463	PMID:20727754	PCS		1/5			C	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0000007	PMID:19503089	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0007256	PMID:20727754	PCS		2/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0000648	PMID:20727754	PCS		2/3			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0001249	PMID:20727754	PCS		5/5			P	HPO:probinson[2020-12-05]
OMIM:619052	Mitochondrial complex IV deficiency, nuclear type 8		HP:0003688	PMID:20727754	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:616361	Parkinson disease 21		HP:0100315	OMIM:616361	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616361	Parkinson disease 21		HP:0002067	OMIM:616361	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616361	Parkinson disease 21		HP:0001300	OMIM:616361	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616361	Parkinson disease 21		HP:0002063	OMIM:616361	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616361	Parkinson disease 21		HP:0002172	OMIM:616361	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616361	Parkinson disease 21		HP:0001337	OMIM:616361	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616361	Parkinson disease 21		HP:0000006	OMIM:616361	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616361	Parkinson disease 21		HP:0003677	OMIM:616361	TAS					C	HPO:skoehler[2015-12-30]
OMIM:609241	Schindler disease, type I		HP:0000486	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0002376	OMIM:609241	TAS					P	HPO:probinson[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0001250	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0001252	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0001263	OMIM:609241	TAS					P	HPO:probinson[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0003461	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0003593	OMIM:609241	TAS					C	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0001290	OMIM:609241	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609241	Schindler disease, type I		HP:4000202	OMIM:609241	TAS					P	HPO:probinson[2024-01-06]
OMIM:609241	Schindler disease, type I		HP:0000639	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0100704	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0000938	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0000007	OMIM:609241	IEA					I	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0000648	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0001257	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0001336	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0001347	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:609241	Schindler disease, type I		HP:0003700	OMIM:609241	IEA					P	HPO:iea[2009-02-17]
OMIM:264500	Pseudouridinuria and mental defect		HP:0001939	OMIM:264500	IEA					P	HPO:iea[2009-02-17]
OMIM:264500	Pseudouridinuria and mental defect		HP:0000007	OMIM:264500	IEA					I	HPO:iea[2009-02-17]
OMIM:264500	Pseudouridinuria and mental defect		HP:0001249	OMIM:264500	IEA					P	HPO:iea[2009-02-17]
OMIM:616407	Brown syndrome		HP:0000651	PMID:1757853	TAS					P	HPO:lccarmody[2019-01-29]
OMIM:616407	Brown syndrome		HP:0031622	PMID:1757853	TAS					P	HPO:lccarmody[2019-01-29]
OMIM:616407	Brown syndrome		HP:0000006	PMID:1757853	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0100864	PMID:28742282	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0002970	PMID:28742282	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0004233	PMID:28742282	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0000926	PMID:28742282	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0008422	PMID:28742282	PCS		2/2			P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0000007	PMID:28742282	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0033102	PMID:28742282	PCS		2/2			P	HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0002656	PMID:28742282	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0003180	PMID:28742282	PCS		2/2			P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0003502	PMID:28742282	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-26]
OMIM:617719	Epiphyseal dysplasia, multiple, 7		HP:0003090	PMID:28742282	PCS		2/2			P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
DECIPHER:72	22q11.2 distal deletion syndrome		HP:0004322	DECIPHER:72	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:72	22q11.2 distal deletion syndrome		HP:0000271	DECIPHER:72	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:72	22q11.2 distal deletion syndrome		HP:0001518	DECIPHER:72	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:72	22q11.2 distal deletion syndrome		HP:0001249	DECIPHER:72	IEA					P	HPO:skoehler[2013-05-29]
OMIM:229400	Frontofacionasal dysplasia		HP:0007835	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0004423	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0004122	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000482	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000581	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0003196	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000518	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000316	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0007541	OMIM:229400	TAS					P	HPO:probinson[2012-07-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000612	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000430	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0005466	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0011803	OMIM:229400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000193	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0007708	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000272	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0011800	OMIM:229400	TAS					P	HPO:skoehler[2013-11-28]
OMIM:229400	Frontofacionasal dysplasia		HP:0000506	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000508	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000007	OMIM:229400	IEA					I	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000568	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0009755	OMIM:229400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:229400	Frontofacionasal dysplasia		HP:0000625	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000202	OMIM:229400	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229400	Frontofacionasal dysplasia		HP:0000204	OMIM:229400	TAS					P	HPO:probinson[2009-02-17]
OMIM:229400	Frontofacionasal dysplasia		HP:0000248	OMIM:229400	IEA					P	HPO:iea[2009-02-17]
DECIPHER:66	15q24 recurrent microdeletion syndrome		HP:0000252	DECIPHER:66	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:66	15q24 recurrent microdeletion syndrome		HP:0004322	DECIPHER:66	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:66	15q24 recurrent microdeletion syndrome		HP:0000271	DECIPHER:66	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:66	15q24 recurrent microdeletion syndrome		HP:0001382	DECIPHER:66	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:66	15q24 recurrent microdeletion syndrome		HP:0001518	DECIPHER:66	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:66	15q24 recurrent microdeletion syndrome		HP:0000047	DECIPHER:66	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:66	15q24 recurrent microdeletion syndrome		HP:0001249	DECIPHER:66	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614204	Psoriasis 14, pustular		HP:0003621	PMID:21848462	PCS		2/14			C	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0001036	PMID:21848462	PCS		8/8			P	HPO:skoehler[2012-11-21];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0025252	PMID:21848462	PCS		4/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0005764	PMID:22903787	IEA		2/14			P	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0000221	PMID:21848462	PCS		4/16			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0200039	PMID:21848462	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0003593	PMID:21848462	PCS		2/14			C	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0025092	PMID:21848462	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0010783	PMID:21848462	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0011227	PMID:22903787;PMID:21848462	PCS		30/30			P	HPO:probinson[2020-10-09];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0011897	PMID:22903787	PCS		14/14			P	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0040313	PMID:22903787;PMID:21848462	PCS		3/30			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0011463	PMID:21848462	PCS		4/14			C	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0011462	PMID:21848462	PCS		3/14			C	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0000007	PMID:21848462	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0030151	PMID:21848462	PCS		3/16			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0001945	PMID:21848462	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0008404	PMID:21848462	PCS		4/16			P	HPO:skoehler[2013-05-03];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0003765	PMID:21848462	PCS		16/16			P	HPO:skoehler[2012-11-21];HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0003765	PMID:22903787	PCS	HP:0003581	14/14			P	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0003623	PMID:21848462	PCS		3/14			C	HPO:probinson[2020-10-09]
OMIM:614204	Psoriasis 14, pustular		HP:0001974	PMID:21848462	PCS		16/16			P	HPO:probinson[2020-10-09];HPO:probinson[2020-10-09]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000286	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0004422	OMIM:605309	IEA					P	HPO:iea[2009-02-17]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000343	OMIM:605309	IEA					P	HPO:iea[2009-02-17]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001252	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0003196	OMIM:605309	IEA					P	HPO:iea[2009-02-17]
OMIM:605309	Macrocephaly/autism syndrome		HP:0002240	OMIM:605309	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:605309	Macrocephaly/autism syndrome		HP:0003593	PMID:15805158	PCS		3/3			C	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0005490	PMID:15805158	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0031447	PMID:15805158	PCS		2/3			P	HPO:probinson[2023-01-23];HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0002719	OMIM:605309	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:605309	Macrocephaly/autism syndrome		HP:0011220	PMID:15805158	PCS		2/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000717	PMID:15805158	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001548	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000337	OMIM:605309	IEA					P	HPO:iea[2009-02-17]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001888	OMIM:605309	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000736	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000218	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001249	OMIM:605309	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001744	OMIM:605309	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000973	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0004313	OMIM:605309	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000750	PMID:15805158	PCS		2/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001520	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000034	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001382	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001263	PMID:15805158	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0011800	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0005280	PMID:15805158	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0012520	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0011098	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000403	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0002208	PMID:15805158	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0002007	OMIM:605309	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605309	Macrocephaly/autism syndrome		HP:0000006	PMID:15805158	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:605309	Macrocephaly/autism syndrome		HP:0001513	OMIM:605309	IEA					P	HPO:iea[2009-02-17]
OMIM:609533	Deafness, autosomal recessive 23		HP:0003577	PMID:14570705	PCS		8/8			C	HPO:probinson[2024-03-14]
OMIM:609533	Deafness, autosomal recessive 23		HP:0000407	PMID:14570705	PCS		8/8			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-14]
OMIM:609533	Deafness, autosomal recessive 23		HP:0000007	PMID:14570705	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609533	Deafness, autosomal recessive 23		HP:0000505	PMID:14570705	PCS		0/8			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000286	PMID:33268356	PCS		9/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001770	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0010804	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000486	PMID:33268356	PCS		7/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001250	PMID:33268356	PCS		17/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001371	PMID:33268356	PCS		10/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002263	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000160	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001252	PMID:33268356	PCS		27/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002020	PMID:33268356	PCS		11/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0045075	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0033725	PMID:33268356	PCS		1/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000639	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000319	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0011220	PMID:33268356	PCS		7/66			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000954	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001647	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000316	PMID:33268356	PCS		8/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0025336	PMID:33268356	PCS		29/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000752	PMID:33268356	PCS		1/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001601	PMID:33268356	PCS		5/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000358	PMID:33268356	PCS		4/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000252	PMID:33268356	PCS		8/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000494	PMID:33268356	PCS		6/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001382	PMID:33268356	PCS		6/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000490	PMID:33268356	PCS		5/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001263	PMID:33268356	PCS		32/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000294	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0011800	PMID:33268356	PCS		4/66			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001182	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000729	PMID:33268356	PCS		2/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001257	PMID:33268356	PCS		6/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000289	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000006	PMID:33268356	PCS					I	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000369	PMID:33268356	PCS		7/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000341	PMID:33268356	PCS		4/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000582	PMID:33268356	PCS		4/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002562	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000343	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002002	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000463	PMID:33268356	PCS		4/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002120	PMID:33268356	PCS		5/28			P	HPO:probinson[2022-05-09];HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001274	PMID:33268356	PCS		1/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002162	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0100704	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0012450	PMID:33268356	PCS		9/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002119	PMID:33268356	PCS		3/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002714	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000256	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001320	PMID:33268356	PCS		1/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000154	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000750	PMID:33268356	PCS		30/31			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0031936	PMID:33268356	PCS		30/31			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002376	PMID:33268356	PCS		5/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000232	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000430	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000194	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0005280	PMID:33268356	PCS		7/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0011304	PMID:33268356	PCS		2/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0012520	PMID:33268356	PCS		1/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0007099	PMID:33268356	PCS		1/32			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000348	PMID:33268356	PCS		4/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001357	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0002007	PMID:33268356	PCS		3/66			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0001631	PMID:33268356	PCS		7/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000347	PMID:33268356	PCS		3/33			P	HPO:probinson[2022-05-09]
OMIM:619720	Bryant-Li-Bhoj neurodevelopmental syndrome 1		HP:0000303	PMID:33268356	PCS		1/33			P	HPO:probinson[2022-05-09]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0002135	PMID:25938945	PCS		15/15			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-04-25]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0003676	OMIM:616413	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0031814	OMIM:616413	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0001300	OMIM:616413	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0001266	OMIM:616413	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0002354	OMIM:616413	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0001250	OMIM:616413	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0001260	OMIM:616413	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0003581	PMID:25938945	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2021-04-25]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0100543	OMIM:616413	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0000716	OMIM:616413	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0000726	OMIM:616413	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0000006	PMID:25938945	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-04-25]
OMIM:616413	Basal ganglia calcification, idiopathic, 6		HP:0004305	OMIM:616413	TAS					P	HPO:skoehler[2015-06-22]
OMIM:157600	Mirror movements 1 and/or agenesis of the corpus callosum		HP:0001274	OMIM:157600	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:157600	Mirror movements 1 and/or agenesis of the corpus callosum		HP:0003829	PMID:20431009	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-10]
OMIM:157600	Mirror movements 1 and/or agenesis of the corpus callosum		HP:0003593	PMID:20431009	PCS					C	HPO:probinson[2023-06-10]
OMIM:157600	Mirror movements 1 and/or agenesis of the corpus callosum		HP:0001335	OMIM:157600	IEA					P	HPO:iea[2009-02-17]
OMIM:157600	Mirror movements 1 and/or agenesis of the corpus callosum		HP:0000006	PMID:20431009	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-10]
OMIM:607278	Osteofibrous dysplasia, susceptibility to		HP:0003038	OMIM:607278	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:607278	Osteofibrous dysplasia, susceptibility to		HP:0005864	OMIM:607278	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-15]
OMIM:607278	Osteofibrous dysplasia, susceptibility to		HP:0003577	PMID:16203897	PCS					C	HPO:probinson[2022-08-15];HPO:probinson[2022-08-15]
OMIM:607278	Osteofibrous dysplasia, susceptibility to		HP:0000767	PMID:26637977	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-15]
OMIM:607278	Osteofibrous dysplasia, susceptibility to		HP:0002756	PMID:16203897	PCS	HP:0011463	6/6			P	HPO:probinson[2022-08-15];HPO:probinson[2022-08-15]
OMIM:607278	Osteofibrous dysplasia, susceptibility to		HP:0000006	PMID:26637977	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-15]
OMIM:618358	Cone-rod dystrophy and hearing loss 2		HP:0000613	PMID:29718797	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-23]
OMIM:618358	Cone-rod dystrophy and hearing loss 2		HP:0001757	PMID:29718797	PCS		2/2			P	HPO:probinson[2021-05-23]
OMIM:618358	Cone-rod dystrophy and hearing loss 2		HP:0000007	PMID:29718797	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-23]
OMIM:618358	Cone-rod dystrophy and hearing loss 2		HP:0007663	PMID:29718797	PCS		2/2			P	HPO:probinson[2021-05-23]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001251	PMID:15455402;PMID:10767350	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0003593	PMID:12928484	PCS		1/2			C	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001290	PMID:10767350	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001290	PMID:12928484	PCS	HP:0003623	2/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001290	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001508	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0000639	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0000817	PMID:10767350	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0012692	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0008872	PMID:12928484	PCS	HP:0003623	1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0008358	PMID:12928484	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0000713	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001324	PMID:10767350	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001522	PMID:15455402;PMID:12928484	PCS		3/3			C	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0003688	PMID:15455402;PMID:10767350;PMID:12928484	PCS		3/3			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001942	PMID:12928484	PCS	HP:0003623	1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001942	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001744	PMID:12928484	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001348	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0003623	PMID:12928484	PCS		1/2			C	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0003128	PMID:12928484	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0003348	PMID:12928484	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0002133	PMID:10767350	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0003542	PMID:12928484	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0002151	PMID:15455402;PMID:10767350	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0002490	PMID:15455402;PMID:10767350	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0032988	PMID:15455402	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0000407	PMID:12928484	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0000508	PMID:10767350	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0000007	PMID:10767350	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001998	PMID:12928484	IEA	HP:0003623	1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001638	PMID:12928484	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619046	Mitochondrial complex IV deficiency, nuclear type 3		HP:0001972	PMID:12928484	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:185020	Cryohydrocytosis		HP:0004446	PMID:16227998	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:185020	Cryohydrocytosis		HP:0001878	PMID:16227998	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:185020	Cryohydrocytosis		HP:0001923	OMIM:185020	TAS					P	HPO:skoehler[2015-12-30]
OMIM:185020	Cryohydrocytosis		HP:4000194	PMID:16227998	PCS					P	HPO:probinson[2024-01-06]
OMIM:185020	Cryohydrocytosis		HP:0000006	PMID:16227998	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:185020	Cryohydrocytosis		HP:0001744	PMID:16227998	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-26]
OMIM:609255	Febrile seizures, familial, 5		HP:0002069	OMIM:609255	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609255	Febrile seizures, familial, 5		HP:0002373	PMID:12429594	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609255	Febrile seizures, familial, 5		HP:0011463	PMID:12429594;OMIM:609255	PCS		20/20			C	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:609255	Febrile seizures, familial, 5		HP:0010819	OMIM:609255	TAS					P	HPO:probinson[2009-02-17]
OMIM:609255	Febrile seizures, familial, 5		HP:0010818	OMIM:609255	TAS					P	HPO:probinson[2009-02-17]
OMIM:609255	Febrile seizures, familial, 5		HP:0003593	PMID:12429594	PCS					C	HPO:probinson[2022-09-02]
OMIM:609255	Febrile seizures, familial, 5		HP:0000006	PMID:12429594	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:153300	Yellow nail syndrome		HP:0008383	OMIM:153300	IEA					P	HPO:iea[2009-02-17]
OMIM:153300	Yellow nail syndrome		HP:0003550	OMIM:153300	IEA					P	HPO:iea[2009-02-17]
OMIM:153300	Yellow nail syndrome		HP:0011367	OMIM:153300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:153300	Yellow nail syndrome		HP:0003759	OMIM:153300	TAS					P	HPO:probinson[2009-02-17]
OMIM:153300	Yellow nail syndrome		HP:0001004	OMIM:153300	TAS					P	HPO:probinson[2009-02-17]
OMIM:153300	Yellow nail syndrome		HP:0000006	OMIM:153300	IEA					I	HPO:iea[2009-02-17]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003477	PMID:12244316	PCS					P	HPO:probinson[2013-03-02];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0002059	PMID:12244316	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003621	PMID:12244316	PCS		3/3			C	HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003431	PMID:12244316	PCS		1/3			P	HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0006858	PMID:12244316	PCS		3/3			P	HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003376	PMID:12244316	PCS		3/3			P	HPO:probinson[2013-03-02];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003124	PMID:12244316	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0001761	PMID:12244316	PCS		3/3			P	HPO:probinson[2013-03-02];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0001272	PMID:12244316	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003693	PMID:12244316	PCS		3/3			P	HPO:probinson[2013-03-02]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0001250	PMID:12244316	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0001260	PMID:12244316	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0002495	PMID:12244316	PCS		3/3			P	HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0001284	PMID:12244316	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0001251	PMID:12244316	PCS		3/3			P	HPO:probinson[2013-03-02];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003073	PMID:12244316	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0003380	PMID:12244316	PCS		1/1			P	HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0000007	PMID:12244316	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0002936	PMID:12244316	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0000763	PMID:12244316	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1		HP:0001249	PMID:12244316	PCS		0/3			P	HPO:probinson[2023-05-21]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0003653	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000365	PMID:20825431	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001250	PMID:20825431	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001670	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002240	PMID:20825431	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0100790	OMIM:252930	TAS					P	HPO:skoehler[2013-05-29]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000280	PMID:20825431	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001270	OMIM:252930	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0011463	PMID:20825431	PCS		6/8			C	HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001507	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0003309	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000998	PMID:20825431	PCS		2/11			P	HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000752	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000510	OMIM:252930	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002159	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001007	PMID:20825431	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001249	PMID:20825431	PCS		7/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001744	PMID:20825431	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002014	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002751	PMID:20825431	PCS		2/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002333	OMIM:252930;PMID:20825431	PCS		12/21			P	HPO:probinson[2022-08-18];HPO:skoehler[2012-10-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002015	PMID:20825431	PCS		4/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0003621	PMID:20825431	PCS		2/8			C	HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000232	OMIM:252930	IEA					P	HPO:skoehler[2010-06-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001387	PMID:20825431	PCS		2/11			P	HPO:probinson[2012-05-05];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002371	PMID:20825431	PCS	HP:0011463	4/11			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0001263	PMID:20825431	PCS		3/11			P	HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000250	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000943	PMID:20825431	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000007	PMID:20825431	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002208	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000900	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000268	OMIM:252930	IEA					P	HPO:skoehler[2010-06-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0002788	OMIM:252930	IEA					P	HPO:iea[2009-02-17]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0000664	PMID:20825431	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:252930	Mucopolysaccharidosis type IIIC		HP:0004568	PMID:20825431	PCS		1/11			P	HPO:probinson[2022-08-18]
OMIM:156250	Metachondromatosis		HP:0002762	PMID:21533187;PMID:20577567	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156250	Metachondromatosis		HP:0005655	OMIM:156250	IEA					P	HPO:iea[2009-02-17]
OMIM:156250	Metachondromatosis		HP:0000494	PMID:21533187;PMID:20577567	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156250	Metachondromatosis		HP:0000316	PMID:21533187;PMID:20577567	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156250	Metachondromatosis		HP:0006487	OMIM:156250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:156250	Metachondromatosis		HP:0000465	PMID:21533187;PMID:20577567	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156250	Metachondromatosis		HP:0001642	PMID:21533187;PMID:20577567	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156250	Metachondromatosis		HP:0001367	OMIM:156250	IEA					P	HPO:iea[2009-02-17]
OMIM:156250	Metachondromatosis		HP:0000358	PMID:21533187;PMID:20577567	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156250	Metachondromatosis		HP:0001249	PMID:21533187;PMID:20577567	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:156250	Metachondromatosis		HP:0000006	PMID:21533187	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-24]
OMIM:156250	Metachondromatosis		HP:0005701	PMID:21533187;PMID:20577567	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-24];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:615654	Deafness, autosomal dominant 58		HP:0003621	PMID:32337552	PCS		1/16			C	HPO:probinson[2024-03-15]
OMIM:615654	Deafness, autosomal dominant 58		HP:0011463	PMID:32337552	PCS		1/16			C	HPO:probinson[2024-03-15]
OMIM:615654	Deafness, autosomal dominant 58		HP:0000407	PMID:32337552	PCS		20/20			P	HPO:probinson[2024-03-15]
OMIM:615654	Deafness, autosomal dominant 58		HP:0011462	PMID:32337552	PCS		14/16			C	HPO:probinson[2024-03-15]
OMIM:615654	Deafness, autosomal dominant 58		HP:0000360	PMID:32337552	PCS		15/19			P	HPO:skoehler[2014-02-25];HPO:probinson[2024-03-15]
OMIM:615654	Deafness, autosomal dominant 58		HP:0007663	PMID:32337552	PCS		0/20			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:615654	Deafness, autosomal dominant 58		HP:0000006	PMID:32337552	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2024-03-15]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0001892	PMID:7727776	PCS		2/2			P	HPO:probinson[2012-07-21];HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0003577	OMIM:613225	TAS					C	HPO:skoehler[2010-06-19]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0031364	PMID:7727776	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0005261	OMIM:613225	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0002170	OMIM:613225	TAS					P	HPO:probinson[2012-07-21]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0011884	PMID:7727776	PCS		2/2			P	HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0040233	PMID:7727776	PCS		2/2			P	HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0007420	PMID:7727776	PCS		1/2			P	HPO:probinson[2012-07-21];HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0000007	PMID:7727776	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0000978	PMID:7727776	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0008357	PMID:7727776	PCS		2/2			P	HPO:probinson[2012-07-21];HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0001934	PMID:7727776	PCS		1/2			P	HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0000421	OMIM:613225	TAS					P	HPO:skoehler[2010-06-19]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0003623	PMID:7727776	IEA		2/2			C	HPO:probinson[2022-03-28]
OMIM:613225	Factor XIII, A subunit, deficiency of		HP:0000225	PMID:7727776	PCS		2/2			P	HPO:probinson[2022-03-28]
OMIM:612885	Premature ovarian failure 10		HP:0008209	PMID:25437880	PCS					P	HPO:skoehler[2015-12-30]
OMIM:612885	Premature ovarian failure 10		HP:0011969	OMIM:612885	TAS					P	HPO:skoehler[2015-12-30]
OMIM:612885	Premature ovarian failure 10		HP:0008232	PMID:25437880	PCS					P	HPO:skoehler[2015-12-30]
OMIM:612885	Premature ovarian failure 10		HP:0000821	PMID:25437880	PCS					P	HPO:skoehler[2015-08-16]
OMIM:612885	Premature ovarian failure 10		HP:0000007	PMID:25437880	PCS					I	HPO:skoehler[2015-12-30]
OMIM:612885	Premature ovarian failure 10		HP:0008734	OMIM:612885	TAS			MALE		P	HPO:skoehler[2015-10-05]
OMIM:612885	Premature ovarian failure 10		HP:0000786	PMID:25437880	PCS					P	HPO:skoehler[2015-08-16]
OMIM:612885	Premature ovarian failure 10		HP:0000027	OMIM:612885	TAS			MALE		P	HPO:skoehler[2015-10-05]
OMIM:612885	Premature ovarian failure 10		HP:0008724	PMID:25437880	PCS			FEMALE		P	HPO:probinson[2017-05-29]
OMIM:605321	Frontoocular syndrome		HP:0000286	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000582	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000486	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000243	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0001052	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000160	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000581	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0001076	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0004440	OMIM:605321	TAS					P	HPO:skoehler[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0012745	OMIM:605321	TAS					P	HPO:skoehler[2014-03-24]
OMIM:605321	Frontoocular syndrome		HP:0000218	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0001642	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000358	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0005306	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0011829	OMIM:605321	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605321	Frontoocular syndrome		HP:0001263	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0003186	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0009891	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000508	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000426	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000767	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000601	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000520	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0001631	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000006	OMIM:605321	IEA					I	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000347	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000369	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:605321	Frontoocular syndrome		HP:0000545	OMIM:605321	IEA					P	HPO:iea[2009-02-17]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0000143	PMID:34415310	PCS		1/9			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0010946	PMID:34415310	PCS		2/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002089	PMID:34415310	PCS		1/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001310	PMID:34415310	PCS		2/5			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001332	PMID:34415310	PCS		2/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0030674	PMID:34415310	PCS		10/14			C	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001250	PMID:34415310	PCS		4/11			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001272	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0003593	PMID:34415310	PCS		2/14			C	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001251	PMID:34415310	PCS		2/5			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0010862	PMID:34415310	PCS		6/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002080	PMID:34415310	PCS		3/5			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0033725	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0012110	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0010292	PMID:34415310	PCS		1/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0000639	PMID:34415310	PCS		4/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0011463	PMID:34415310	PCS		2/14			C	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0011100	PMID:34415310	PCS		5/13			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001888	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0020045	PMID:34415310	PCS		1/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0007663	PMID:34415310	PCS		2/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0003429	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002415	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001249	PMID:34415310	PCS		6/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002599	PMID:34415310	PCS		1/5			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002037	PMID:34415310	PCS		6/7			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002015	PMID:34415310	PCS		6/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0000750	PMID:34415310	PCS		6/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001321	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002110	PMID:34415310	PCS		1/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001263	PMID:34415310	PCS		6/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002194	PMID:34415310	PCS		6/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0010557	PMID:34415310	PCS		1/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0032965	PMID:34415310	PCS		1/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0006380	PMID:34415310	PCS		2/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002808	PMID:34415310	PCS		3/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0030890	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0000007	PMID:34415310	PCS					I	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0000648	PMID:34415310	PCS		1/6			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0000268	PMID:34415310	PCS		2/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002126	PMID:34415310	PCS		3/10			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0000347	PMID:34415310	PCS		3/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0001776	PMID:34415310	PCS		3/14			P	HPO:probinson[2022-03-07]
OMIM:619708	Gastrointestinal defects and immunodeficiency syndrome 2		HP:0002721	PMID:34415310	PCS					P	HPO:probinson[2022-03-07]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000341	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0003764	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000252	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0030434	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0001761	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000490	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0030079	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0001263	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0011800	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000639	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0011463	PMID:36322655	PCS		1/1			C	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0040276	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0012032	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000007	PMID:36322655	PCS					I	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0006743	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000358	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000347	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0005701	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0000962	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0005987	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:620189	Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition		HP:0001765	PMID:36322655	PCS		1/1			P	HPO:probinson[2023-06-17]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003236	OMIM:618416	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001332	OMIM:618416	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001250	OMIM:618416	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001251	OMIM:618416	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003593	PMID:26541337	PCS		1/1			C	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001290	OMIM:618416	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001270	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0030319	PMID:26541337	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001987	OMIM:618416	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0025336	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0002359	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003701	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003688	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003128	PMID:26541337	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0000750	OMIM:618416	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0002650	PMID:26541337	PCS		1/1		HP:0012825	P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003200	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001266	OMIM:618416	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0031936	PMID:26541337	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0002376	OMIM:618416	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003201	PMID:26541337	PCS		0/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003388	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001260	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0001263	OMIM:618416	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0002151	PMID:26541337	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0003738	PMID:26541337	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:618416	Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression		HP:0000007	PMID:26541337	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-22]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000286	PMID:28805828	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0003774	PMID:28805828	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000365	PMID:28805828	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000276	PMID:28805828	PCS		1/1			P	HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000490	PMID:28805828	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0001263	PMID:28805828	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000097	PMID:28805828	PCS		2/2			P	HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0001251	PMID:28805828	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000093	PMID:28805828	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0012444	PMID:28805828	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0012588	PMID:28805828	PCS		2/2			P	HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000969	PMID:28805828	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0011463	PMID:28805828	PCS		2/2			C	HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0011451	PMID:28805828	PCS		2/2			P	HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000316	PMID:28805828	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000007	PMID:28805828	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0006970	PMID:28805828	PCS		1/2			P	HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0002119	PMID:28805828	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0001302	PMID:28805828	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0001257	PMID:28805828	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0000303	PMID:28805828	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0001249	PMID:28805828	PCS		2/2			P	HPO:probinson[2022-11-26]
OMIM:617731	Galloway-Mowat syndrome 5		HP:0009748	PMID:28805828	PCS		1/1			P	HPO:probinson[2022-11-26]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000252	PMID:29522154	PCS		1/5			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000431	PMID:29522154	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000750	PMID:29522154	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0002373	PMID:29522154	PCS	HP:0011463	5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0001250	PMID:29522154	PCS		1/4			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0001263	PMID:29522154	IEA		5/5			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0001252	PMID:29522154	PCS		5/5			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000020	PMID:29522154	PCS		4/4			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0003593	PMID:29522154	PCS		5/5			C	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0001270	PMID:29522154	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0025162	PMID:29522154	PCS		4/4			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000729	PMID:29522154	PCS		1/4			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000316	PMID:29522154	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000007	PMID:28640246	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0002307	PMID:29522154	PCS		5/5			P	HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0000278	PMID:29522154	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0007018	PMID:29522154	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10]
OMIM:618402	Intellectual developmental disorder, autosomal recessive 70		HP:0001249	PMID:28640246;PMID:29522154	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410059	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410057	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410058	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0001250	OMIM:608611	IEA					P	HPO:iea[2009-02-17]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410055	PMID:14988808	IEA					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0001271	OMIM:608611	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410056	PMID:14988808	IEA					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410075	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0001251	OMIM:608611	IEA					P	HPO:iea[2009-02-17]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410073	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410074	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410071	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410072	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0410070	PMID:14988808	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0007141	OMIM:608611	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0000639	OMIM:608611	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0002311	PMID:31056085	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-07-18]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0025550	PMID:14988808	PCS		20/20			P	HPO:NicoleVasilevsky[2018-02-23];HPO:probinson[2023-07-18]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0002352	OMIM:608611	IEA					P	HPO:iea[2009-02-17]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0001260	OMIM:608611	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0001263	OMIM:608611;PMID:31056085	PCS		11/11			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17];HPO:probinson[2023-07-18]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0034894	OMIM:608611	TAS					P	HPO:probinson[2023-07-18]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0000007	OMIM:608611	IEA					I	HPO:iea[2009-02-17]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0000648	OMIM:608611	IEA					P	HPO:iea[2009-02-17]
OMIM:608611	Ribose 5-phosphate isomerase deficiency		HP:0001257	OMIM:608611	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0000010	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002024	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002783	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0004432	OMIM:209920	IEA					P	HPO:skoehler[2010-06-20]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002583	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0004385	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0005386	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002383	OMIM:209920	IEA					P	HPO:skoehler[2010-06-20]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0001080	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0007041	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0001508	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002728	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0011473	OMIM:209920	TAS					P	HPO:skoehler[2013-06-04]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002718	OMIM:209920	TAS					P	HPO:probinson[2012-04-26]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0006562	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0000007	OMIM:209920	TAS					I	HPO:skoehler[2013-06-23]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0030151	OMIM:209920	IEA					P	HPO:skoehler[2018-10-08]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0004429	OMIM:209920	TAS					P	HPO:probinson[2012-04-26]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002788	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002965	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0002841	OMIM:209920	TAS					P	HPO:probinson[2012-04-26]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0001875	OMIM:209920	IEA					P	HPO:iea[2009-02-17]
OMIM:209920	Bare lymphocyte syndrome, type II		HP:0003139	OMIM:209920	TAS					P	HPO:probinson[2012-04-26]
OMIM:614238	Hypotrichosis 10		HP:0000164	PMID:20544222	PCS		0/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:614238	Hypotrichosis 10		HP:0001597	PMID:20544222	PCS		0/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:614238	Hypotrichosis 10		HP:0002231	PMID:20544222	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:614238	Hypotrichosis 10		HP:0002209	PMID:20544222	PCS		5/5			P	HPO:probinson[2024-03-15]
OMIM:614238	Hypotrichosis 10		HP:0000007	PMID:20544222	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:614238	Hypotrichosis 10		HP:0000653	PMID:20544222	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:614238	Hypotrichosis 10		HP:0045075	PMID:20544222	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0009184	OMIM:216800	TAS					P	HPO:probinson[2012-07-16]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0000175	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0000340	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0000540	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0002673	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0000639	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0005001	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0000007	OMIM:216800	IEA					I	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0001822	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0002857	OMIM:216800	IEA					P	HPO:iea[2009-02-17]
OMIM:216800	Coloboma of macula and skeletal anomalies		HP:0001116	OMIM:216800	TAS					P	HPO:probinson[2009-02-17]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0002257	PMID:23993197	PCS		10/12			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-21]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0004322	OMIM:612649	TAS					P	HPO:probinson[2013-04-06]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0002110	PMID:23993197	PCS		9/12			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-21]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0033036	PMID:23993197	PCS		4/5			P	HPO:probinson[2022-02-28]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0012207	PMID:23993197	PCS		1/1	MALE		P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0011108	PMID:23993197	PCS		10/12			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-21]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0012265	PMID:23993197	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-02-28]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0012260	PMID:23993197	PCS		10/10			P	HPO:probinson[2013-04-07];HPO:probinson[2022-02-28]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0012263	PMID:23993197	PCS		1/1			P	HPO:probinson[2020-07-21];HPO:probinson[2022-02-28]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0000007	PMID:23993197	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2020-07-21]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0002205	OMIM:612649	TAS					P	HPO:probinson[2013-04-06]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0002643	PMID:23993197	PCS	HP:0003623	4/12			P	HPO:probinson[2020-07-21]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0003546	OMIM:612649	TAS					P	HPO:probinson[2013-04-06]
OMIM:612649	Ciliary dyskinesia, primary, 11		HP:0004469	PMID:23993197	PCS		3/12			P	HPO:probinson[2020-07-21]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0002213	PMID:18231121	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0002046	PMID:18231121	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000691	OMIM:129490	IEA					P	HPO:iea[2009-02-17]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0045075	PMID:18231121	PCS		8/10			P	HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0008070	PMID:18231121	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000958	PMID:18231121	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000968	PMID:18231121	PCS					P	HPO:skoehler[2015-01-14];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0001807	PMID:18231121	PCS		1/10			P	HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000668	PMID:18231121	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000966	PMID:18231121	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000653	PMID:18231121	PCS					P	HPO:iea[2012-03-01];HPO:probinson[2022-05-08]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000674	OMIM:129490	IEA					P	HPO:iea[2009-02-17]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0002217	OMIM:129490	IEA					P	HPO:iea[2012-03-01]
OMIM:129490	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant		HP:0000006	PMID:10431241	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:265150	Pulmonary atresia with intact ventricular septum		HP:0000007	OMIM:265150	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:265150	Pulmonary atresia with intact ventricular septum		HP:0004935	OMIM:265150	IEA					P	HPO:iea[2009-02-17]
OMIM:265150	Pulmonary atresia with intact ventricular septum		HP:0010954	OMIM:265150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0002312	PMID:21108402	PCS		2/2			P	HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0001250	PMID:18337561;PMID:21108402	PCS		2/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0002495	PMID:21108402	PCS		1/2			P	HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0001263	PMID:18337561;PMID:21108402	PCS		3/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0003593	PMID:18337561	PCS		5/6			C	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0011463	PMID:18337561	PCS		1/6			C	HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0000407	PMID:21108402	PCS		2/2			P	HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0002718	PMID:18337561	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0000007	PMID:18337561	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0000405	PMID:21108402	PCS		1/2			P	HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0006721	PMID:18337561	PCS		1/6			P	HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0002863	PMID:18337561	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0001249	PMID:21108402	IEA		2/2			P	HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0001875	PMID:18337561	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-13]
OMIM:610738	Neutropenia, severe congenital 3, autosomal recessive		HP:0001875	PMID:21108402	PCS	HP:0003577	2/2			P	HPO:probinson[2021-02-13]
OMIM:618364	Myoclonus, familial, 2		HP:0001332	PMID:29726066	PCS		0/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13];HPO:probinson[2024-03-15]
OMIM:618364	Myoclonus, familial, 2		HP:0031936	PMID:29726066	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618364	Myoclonus, familial, 2		HP:0001250	PMID:29726066	IEA		0/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13];HPO:probinson[2024-03-15]
OMIM:618364	Myoclonus, familial, 2		HP:0003680	PMID:29726066	PCS					C	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:618364	Myoclonus, familial, 2		HP:0000006	PMID:29726066	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:618364	Myoclonus, familial, 2		HP:0001249	PMID:29726066	PCS		0/2			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:618364	Myoclonus, familial, 2		HP:0045084	PMID:29726066	PCS	HP:0003621	5/5			P	HPO:probinson[2019-06-13]
OMIM:615907	Lymphatic malformation 4		HP:0100797	OMIM:615907	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615907	Lymphatic malformation 4		HP:0000034	PMID:23410910	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-18]
OMIM:615907	Lymphatic malformation 4		HP:0011463	PMID:23410910	PCS		3/3			C	HPO:probinson[2023-02-18]
OMIM:615907	Lymphatic malformation 4		HP:0100658	PMID:23410910	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:615907	Lymphatic malformation 4		HP:0010741	PMID:23410910	PCS		4/7			P	HPO:probinson[2023-02-18]
OMIM:615907	Lymphatic malformation 4		HP:0001004	PMID:23410910	PCS		7/7			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-18]
OMIM:615907	Lymphatic malformation 4		HP:0001015	PMID:23410910	PCS		4/7			P	HPO:probinson[2023-02-18]
OMIM:615907	Lymphatic malformation 4		HP:0000006	PMID:23410910	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-18]
OMIM:615907	Lymphatic malformation 4		HP:0000962	PMID:23410910	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:267800	Retinal dystrophy, reticular pigmentary, of posterior pole		HP:0007937	OMIM:267800	TAS					P	HPO:iea[2009-02-17]
OMIM:267800	Retinal dystrophy, reticular pigmentary, of posterior pole		HP:0000007	OMIM:267800	TAS					I	HPO:iea[2009-02-17]
OMIM:267800	Retinal dystrophy, reticular pigmentary, of posterior pole		HP:0011510	OMIM:267800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267800	Retinal dystrophy, reticular pigmentary, of posterior pole		HP:0000556	OMIM:267800	TAS					P	HPO:iea[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000286	PMID:32071410	PCS		5/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0002221	OMIM:259050	IEA					P	HPO:probinson[2012-02-20]
OMIM:259050	Primrose syndrome		HP:0000365	PMID:25017102;PMID:32071410	PCS		12/14			P	HPO:probinson[2022-06-04];HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000486	PMID:32071410	PCS		3/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0004322	OMIM:259050	TAS					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0001371	PMID:25017102	PCS		5/7			P	HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0001250	PMID:32071410	PCS		0/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000160	PMID:32071410	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0003273	OMIM:259050	TAS					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0001252	PMID:25017102;PMID:32071410	PCS		11/14			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-08-20];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0001251	PMID:32071410	PCS		2/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0002180	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000718	PMID:25017102	PCS		1/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0011220	PMID:32071410	PCS		3/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000717	PMID:25017102;PMID:32071410	PCS		4/14			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000316	PMID:32071410	PCS		0/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000711	OMIM:259050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:259050	Primrose syndrome		HP:0002857	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0003745	OMIM:259050	IEA					I	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0001840	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0001249	PMID:25017102	PCS		5/8			P	HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0003623	PMID:32071410	PCS		5/6			C	HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0003202	PMID:32071410	PCS		1/6			P	HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000494	PMID:25017102;PMID:32071410	PCS		11/14			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0001385	PMID:25017102	PCS		4/8			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0005103	PMID:25017102;PMID:32071410	PCS		8/14			P	HPO:probinson[2022-06-04];HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000771	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0002079	PMID:25017102	PCS		5/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0001382	PMID:32071410	PCS		3/6			P	HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0002550	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000490	PMID:25017102	PCS		7/8			P	HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0002231	PMID:25017102	PCS		7/8			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0001263	PMID:32071410	PCS		6/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0011800	OMIM:259050	TAS					P	HPO:skoehler[2013-11-28]
OMIM:259050	Primrose syndrome		HP:0006380	OMIM:259050	TAS					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000327	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0040309	PMID:25017102	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000767	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0002868	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000400	PMID:25017102;PMID:32071410	PCS		12/14			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0008689	OMIM:259050	TAS		HP:0040283			P	HPO:skoehler[2014-09-21]
OMIM:259050	Primrose syndrome		HP:0000006	PMID:25017102	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000248	PMID:25017102	PCS		6/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0003577	PMID:32071410	PCS		1/6			C	HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000463	PMID:32071410	PCS		2/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0003693	PMID:25017102	PCS		7/8			P	HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0040160	OMIM:259050	TAS					P	HPO:skoehler[2015-06-22]
OMIM:259050	Primrose syndrome		HP:0100033	PMID:25017102	PCS		1/8			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000819	PMID:25017102	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0008391	OMIM:259050	IEA					P	HPO:skoehler[2019-09-07]
OMIM:259050	Primrose syndrome		HP:0000939	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000815	OMIM:259050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:259050	Primrose syndrome		HP:0100789	PMID:25017102	PCS		2/8			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000739	PMID:25017102;PMID:32071410	PCS		3/14			P	HPO:probinson[2021-08-20];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0009882	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0006254	PMID:25017102	PCS		5/5			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000337	PMID:25017102	PCS		7/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000733	PMID:25017102;PMID:32071410	PCS		5/14			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0002119	PMID:32071410	PCS		3/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0002714	PMID:32071410	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000218	PMID:32071410	PCS		1/6			P	HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000455	PMID:25017102	PCS		2/8			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000774	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0002514	PMID:25017102;PMID:32071410	PCS		4/14			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000256	PMID:25017102	PCS		5/8			P	HPO:probinson[2009-02-17];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000256	PMID:32071410	IEA	HP:0003577	3/5			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000179	PMID:25017102	PCS		6/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0003301	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000750	PMID:32071410	PCS		6/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0000431	PMID:32071410	PCS		0/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0001761	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000272	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0005121	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0005280	PMID:32071410	PCS		0/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0100753	PMID:32071410	PCS		1/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0002808	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0008541	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000508	PMID:25017102;PMID:32071410	PCS		10/14			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04];HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0002209	OMIM:259050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259050	Primrose syndrome		HP:0000821	PMID:32071410	PCS		2/6			P	HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0100716	PMID:25017102	PCS		4/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0001956	PMID:25017102	PCS		5/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0000823	PMID:32071410	PCS		1/2			P	HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0001115	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0000664	OMIM:259050	IEA					P	HPO:probinson[2009-02-17]
OMIM:259050	Primrose syndrome		HP:0007018	PMID:32071410	PCS		0/6			P	HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:259050	Primrose syndrome		HP:0005758	OMIM:259050	TAS					P	HPO:skoehler[2013-10-22]
OMIM:259050	Primrose syndrome		HP:0000028	PMID:25017102	PCS		3/4			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0004349	PMID:25017102	PCS		5/8			P	HPO:probinson[2021-08-20]
OMIM:259050	Primrose syndrome		HP:0001952	OMIM:259050	IEA					P	HPO:skoehler[2018-10-08]
OMIM:234280	Hallux varus and preaxial polysyndactyly		HP:0001177	OMIM:234280	IEA					P	HPO:iea[2009-02-17]
OMIM:234280	Hallux varus and preaxial polysyndactyly		HP:0010055	OMIM:234280	IEA					P	HPO:iea[2009-02-17]
OMIM:234280	Hallux varus and preaxial polysyndactyly		HP:0000007	OMIM:234280	IEA					I	HPO:iea[2009-02-17]
OMIM:234280	Hallux varus and preaxial polysyndactyly		HP:0001159	OMIM:234280	IEA					P	HPO:skoehler[2010-06-20]
OMIM:234280	Hallux varus and preaxial polysyndactyly		HP:0008080	OMIM:234280	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002344	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000684	PMID:10739753	PCS		2/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001371	PMID:10739753	PCS		2/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001250	PMID:10739753	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001252	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0004681	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002180	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000518	PMID:10739753	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000639	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000598	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001007	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002751	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000252	PMID:10739753	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002673	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000490	PMID:10739753	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001263	PMID:10739753	PCS		3/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0012385	OMIM:214150	TAS					P	HPO:skoehler[2013-10-22]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0006380	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000407	PMID:10739753	PCS		1/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002506	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000448	PMID:10739753	PCS		2/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0008125	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000007	PMID:10739753	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000568	PMID:10739753	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002987	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000340	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0003577	PMID:10739753	PCS		3/3			C	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000343	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001272	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001274	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000581	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0012448	OMIM:214150	TAS					P	HPO:skoehler[2013-11-28]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0012444	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000939	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001508	PMID:10739753	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000616	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001944	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000855	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002119	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0006532	PMID:10739753	PCS		3/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0006610	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0007305	PMID:10739753	PCS		2/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001942	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001347	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0008936	PMID:10739753	PCS		3/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002135	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000670	PMID:10739753	PCS		1/3			P	HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000233	OMIM:214150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001321	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002171	PMID:10739753	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0003819	OMIM:214150	TAS					C	HPO:skoehler[2012-10-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001838	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0009473	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0001518	PMID:10739753	PCS		3/3			P	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000426	OMIM:214150	IEA					P	HPO:iea[2009-02-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0002804	OMIM:214150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000028	PMID:10739753	PCS		1/1	MALE		P	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:214150	Cerebrooculofacioskeletal syndrome 1		HP:0000347	PMID:10739753	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:619697	Oocyte maturation defect 12		HP:0008222	PMID:34052850	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619697	Oocyte maturation defect 12		HP:0000007	PMID:34052850	PCS					I	HPO:probinson[2022-03-20]
OMIM:619697	Oocyte maturation defect 12		HP:0033335	PMID:34052850	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002069	PMID:28626029	PCS		6/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0003676	PMID:28626029	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0000486	PMID:28626029	PCS		4/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0004322	PMID:28626029	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0001272	PMID:28626029	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002120	PMID:28626029	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002066	PMID:28626029	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0001252	PMID:28626029	PCS		6/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0003593	PMID:28626029	PCS		1/5			C	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0010862	PMID:28626029	PCS		6/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0011463	PMID:28626029	PCS		4/5			C	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0000733	PMID:28626029	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0007366	PMID:28626029	PCS		4/4			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002119	PMID:28626029	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0001324	PMID:28626029	PCS		6/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0001347	PMID:28626029	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0000253	PMID:28626029	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002378	PMID:28626029	PCS		4/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002015	PMID:28626029	PCS		1/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002136	PMID:28626029	PCS		4/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0001344	PMID:28626029	PCS		3/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002079	PMID:28626029	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0001263	PMID:28626029	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0002194	PMID:28626029	PCS		6/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0100023	PMID:28626029	PCS		6/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0033044	PMID:28626029	PCS		2/6			P	HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0000007	PMID:28626029	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:617862	Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy		HP:0000666	PMID:28626029	PCS		3/6			P	HPO:probinson[2022-10-11]
OMIM:300643	Rolandic epilepsy, impaired intellectual development, and speech dyspraxia		HP:0032407	PMID:16497722	IEA					P	HPO:probinson[2021-05-02]
OMIM:300643	Rolandic epilepsy, impaired intellectual development, and speech dyspraxia		HP:0001250	OMIM:300643	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300643	Rolandic epilepsy, impaired intellectual development, and speech dyspraxia		HP:0011098	OMIM:300643	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300643	Rolandic epilepsy, impaired intellectual development, and speech dyspraxia		HP:0007359	OMIM:300643	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300643	Rolandic epilepsy, impaired intellectual development, and speech dyspraxia		HP:0000006	PMID:16497722	IEA					I	HPO:skoehler[2013-01-11];HPO:probinson[2021-05-02]
OMIM:300125	Migraine, familial typical, susceptibility to, 2		HP:0002013	OMIM:300125	IEA					P	HPO:iea[2009-02-17]
OMIM:300125	Migraine, familial typical, susceptibility to, 2		HP:0002077	OMIM:300125	IEA					P	HPO:iea[2009-02-17]
OMIM:300125	Migraine, familial typical, susceptibility to, 2		HP:0000613	OMIM:300125	IEA					P	HPO:iea[2009-02-17]
OMIM:300125	Migraine, familial typical, susceptibility to, 2		HP:0002083	OMIM:300125	IEA					P	HPO:iea[2009-02-17]
OMIM:300125	Migraine, familial typical, susceptibility to, 2		HP:0002183	OMIM:300125	IEA					P	HPO:iea[2009-02-17]
OMIM:300125	Migraine, familial typical, susceptibility to, 2		HP:0001417	OMIM:300125	IEA					I	HPO:iea[2009-02-17]
OMIM:300125	Migraine, familial typical, susceptibility to, 2		HP:0002018	OMIM:300125	IEA					P	HPO:iea[2009-02-17]
OMIM:613392	Deafness, autosomal recessive 85		HP:0000007	PMID:19888295	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-01-15]
OMIM:613392	Deafness, autosomal recessive 85		HP:0000399	PMID:19888295	PCS	HP:0003577				P	HPO:probinson[2019-04-20]
OMIM:218030	Apparent mineralocorticoid excess		HP:0004322	OMIM:218030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218030	Apparent mineralocorticoid excess		HP:0001508	OMIM:218030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218030	Apparent mineralocorticoid excess		HP:0001095	OMIM:218030	IEA					P	HPO:iea[2009-02-17]
OMIM:218030	Apparent mineralocorticoid excess		HP:0001518	OMIM:218030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:218030	Apparent mineralocorticoid excess		HP:0011463	PMID:7670488	PCS					C	HPO:probinson[2022-09-29]
OMIM:218030	Apparent mineralocorticoid excess		HP:0003351	PMID:7670488	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:218030	Apparent mineralocorticoid excess		HP:0000822	PMID:7670488	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:218030	Apparent mineralocorticoid excess		HP:0200114	OMIM:218030	TAS					P	HPO:skoehler[2013-06-05]
OMIM:218030	Apparent mineralocorticoid excess		HP:0000007	PMID:7670488	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:218030	Apparent mineralocorticoid excess		HP:0002900	PMID:7670488	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:218030	Apparent mineralocorticoid excess		HP:0004319	PMID:7670488	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:218030	Apparent mineralocorticoid excess		HP:0001510	OMIM:218030	IEA					P	HPO:iea[2009-02-17]
OMIM:126600	Doyne honeycomb retinal dystrophy		HP:0007937	OMIM:126600	TAS					P	HPO:probinson[2009-02-17]
OMIM:126600	Doyne honeycomb retinal dystrophy		HP:0000505	OMIM:126600	TAS					P	HPO:probinson[2015-07-19]
OMIM:126600	Doyne honeycomb retinal dystrophy		HP:0000006	OMIM:126600	TAS					I	HPO:probinson[2009-02-17]
OMIM:126600	Doyne honeycomb retinal dystrophy		HP:0000556	OMIM:126600	TAS					P	HPO:skoehler[2015-01-27]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0000508	OMIM:311000	IEA					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0000602	OMIM:311000	IEA					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0000546	OMIM:311000	TAS					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0007686	OMIM:311000	TAS					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0001417	OMIM:311000	IEA					I	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0002414	OMIM:311000	IEA					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0003438	OMIM:311000	TAS					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0200065	OMIM:311000	TAS					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0000545	OMIM:311000	IEA					P	HPO:probinson[2009-02-17]
OMIM:311000	Ophthalmoplegia, external, and myopia		HP:0006844	OMIM:311000	TAS					P	HPO:probinson[2009-02-17]
OMIM:619867	Spermatogenic failure 72		HP:0033393	PMID:32323121	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0032560	PMID:32323121	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0034011	PMID:32323121	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0003251	PMID:32323121	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0011462	PMID:32323121	PCS		1/1			C	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0000007	PMID:32323121	PCS					I	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0033525	PMID:32323121	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0032558	PMID:32323121	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:619867	Spermatogenic failure 72		HP:0032559	PMID:32323121	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:612932	Glycogen storage disease XIII		HP:0003236	OMIM:612932	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612932	Glycogen storage disease XIII		HP:0009051	OMIM:612932	TAS					P	HPO:skoehler[2012-07-16]
OMIM:612932	Glycogen storage disease XIII		HP:0003581	OMIM:612932	TAS					C	HPO:skoehler[2010-06-19]
OMIM:612932	Glycogen storage disease XIII		HP:0000007	OMIM:612932	TAS					I	HPO:skoehler[2010-06-19]
OMIM:612932	Glycogen storage disease XIII		HP:0034633	PMID:11506403	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:612932	Glycogen storage disease XIII		HP:0003326	OMIM:612932	TAS					P	HPO:skoehler[2010-06-20]
OMIM:612932	Glycogen storage disease XIII		HP:0003546	OMIM:612932	TAS					P	HPO:skoehler[2010-06-19]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0000572	PMID:22499339	PCS		7/8			P	HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0010628	PMID:22499339	PCS		1/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0011968	PMID:22499339	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0002240	PMID:22499339	PCS		6/8			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0003593	PMID:22499339	PCS		2/5			C	HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0011480	PMID:22499339	PCS		1/5			P	HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0001508	PMID:22499339	PCS		2/8			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0011002	PMID:22499339	PCS		8/8			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0001903	PMID:22499339	PCS		6/7			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0011463	PMID:22499339	PCS		3/5			C	HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0000007	PMID:22499339	PCS					I	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0000648	PMID:22499339	PCS		8/8			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0002007	PMID:22499339	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0000256	PMID:22499339	PCS		3/8			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0001873	PMID:22499339	PCS		2/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:615085	Osteopetrosis, autosomal recessive 8		HP:0001744	PMID:22499339	PCS		6/8			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-18]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0005575	PMID:19625716	PCS		7/7			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-18]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0005421	PMID:19625716	PCS		3/7			P	HPO:probinson[2023-02-18]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0000790	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0000093	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0001919	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0001937	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0001903	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0000822	OMIM:612926	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0100519	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0001873	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0000006	PMID:19625716	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0003138	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612926	Hemolytic uremic syndrome, atypical, susceptibility to, 6		HP:0003259	OMIM:612926	TAS					P	HPO:skoehler[2012-10-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0001298	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0002069	OMIM:540000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0003198	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0011675	OMIM:540000	TAS					P	HPO:skoehler[2015-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0000819	OMIM:540000	TAS					P	HPO:skoehler[2015-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0012377	OMIM:540000	TAS					P	HPO:skoehler[2013-10-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0001507	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0100704	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0003828	OMIM:540000	TAS					M	HPO:skoehler[2015-12-30]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0000519	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0001427	OMIM:540000	IEA					I	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0001269	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0003128	OMIM:540000	TAS					P	HPO:probinson[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0003200	OMIM:540000	TAS					P	HPO:probinson[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0008619	OMIM:540000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0002076	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0002572	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0005162	OMIM:540000	IEA					P	HPO:skoehler[2019-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0000408	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0000726	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0001716	OMIM:540000	TAS					P	HPO:skoehler[2015-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0000822	OMIM:540000	TAS					P	HPO:skoehler[2015-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0000602	OMIM:540000	TAS					P	HPO:skoehler[2015-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0001635	OMIM:540000	TAS					P	HPO:skoehler[2015-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0001712	OMIM:540000	TAS					P	HPO:skoehler[2015-02-22]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0003737	OMIM:540000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:540000	Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes		HP:0002401	OMIM:540000	IEA					P	HPO:iea[2009-02-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0002553	OMIM:605282	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000175	OMIM:605282	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0001234	PMID:21129728	PCS		10/10			P	HPO:skoehler[2013-01-22];HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0008619	PMID:21129728	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0002002	OMIM:605282	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0001156	OMIM:605282	IEA					P	HPO:skoehler[2015-01-19]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000691	PMID:21129728	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000592	OMIM:605282	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0001263	PMID:21129728	PCS		6/9			P	HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0010049	OMIM:605282	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0010743	OMIM:605282	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0011087	PMID:21129728	PCS		7/10			P	HPO:skoehler[2013-01-22];HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000316	PMID:21129728	PCS					P	HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000007	PMID:21129728	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000648	OMIM:605282	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0008368	OMIM:605282	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0030084	PMID:21129728	PCS		10/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000664	OMIM:605282	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0001159	PMID:21129728	PCS		10/10			P	HPO:skoehler[2013-01-22];HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0009702	OMIM:605282	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0001357	PMID:21129728	PCS					P	HPO:probinson[2019-04-15]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0000699	OMIM:605282	TAS					P	HPO:skoehler[2013-01-22]
OMIM:605282	Temtamy preaxial brachydactyly syndrome		HP:0002974	OMIM:605282	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:211000	Blue diaper syndrome		HP:0000121	OMIM:211000	IEA					P	HPO:iea[2009-02-17]
OMIM:211000	Blue diaper syndrome		HP:0004365	PMID:14246093	TAS					P	HPO:nvasilevsky[2019-03-12]
OMIM:211000	Blue diaper syndrome		HP:0001438	OMIM:211000	IEA					P	HPO:iea[2009-02-17]
OMIM:211000	Blue diaper syndrome		HP:0000007	OMIM:211000	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:211000	Blue diaper syndrome		HP:0003072	OMIM:211000	IEA					P	HPO:iea[2009-02-17]
OMIM:211000	Blue diaper syndrome		HP:0001417	PMID:14246093	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:130710	Emphysema, congenital lobar		HP:0006539	OMIM:130710	IEA					P	HPO:iea[2009-02-17]
OMIM:130710	Emphysema, congenital lobar		HP:0002098	OMIM:130710	IEA					P	HPO:skoehler[2010-06-20]
OMIM:130710	Emphysema, congenital lobar		HP:0000006	OMIM:130710	IEA					I	HPO:iea[2009-02-17]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000286	PMID:33944996	PCS		2/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000582	PMID:33944996	PCS		3/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0001250	PMID:33944996	PCS		10/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0001252	PMID:33944996	PCS		7/14			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0003593	PMID:33944996	PCS					C	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0005274	PMID:33944996	PCS		3/16			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0001270	PMID:33944996	PCS		9/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000718	PMID:33944996	PCS		3/11			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0008551	PMID:33944996	PCS		1/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000378	PMID:33944996	PCS		1/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0001249	PMID:33944996	PCS		9/14			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000358	PMID:33944996	PCS		2/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0001363	PMID:33944996	PCS		3/7			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000750	PMID:33944996	PCS		13/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0012166	PMID:33944996	PCS		1/11			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000729	PMID:33944996	PCS		5/11			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000426	PMID:33944996	PCS		3/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000722	PMID:33944996	PCS		3/11			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0100716	PMID:33944996	PCS		3/11			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000664	PMID:33944996	PCS		2/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0002007	PMID:33944996	PCS		2/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0007018	PMID:33944996	PCS		1/11			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000322	PMID:33944996	PCS		3/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000006	PMID:33944996	PCS					I	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000347	PMID:33944996	PCS		2/16			P	HPO:probinson[2022-08-13]
OMIM:619873	Parenti-Mignot neurodevelopmental syndrome		HP:0000369	PMID:33944996	PCS		1/16			P	HPO:probinson[2022-08-13]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0011760	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0000870	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0001442	OMIM:617686	TAS					I	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0003154	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0033794	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0000953	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0000845	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0003118	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:617686	Pituitary adenoma 3, multiple types, somatic		HP:0008291	OMIM:617686	TAS					P	HPO:probinson[2024-12-15]
OMIM:215500	Choroidal dystrophy, central areolar 1		HP:0000580	PMID:22695961	PCS					P	HPO:probinson[2022-09-11]
OMIM:215500	Choroidal dystrophy, central areolar 1		HP:0030491	PMID:22695961	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2022-09-11]
OMIM:215500	Choroidal dystrophy, central areolar 1		HP:0000006	PMID:22695961	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-11]
OMIM:215500	Choroidal dystrophy, central areolar 1		HP:0000533	PMID:22695961	PCS					P	HPO:probinson[2015-07-19];HPO:probinson[2022-09-11]
OMIM:258400	Ophthalmoplegia totalis with ptosis and miosis		HP:0000486	OMIM:258400	IEA					P	HPO:iea[2009-02-17]
OMIM:258400	Ophthalmoplegia totalis with ptosis and miosis		HP:0000616	OMIM:258400	IEA					P	HPO:iea[2009-02-17]
OMIM:258400	Ophthalmoplegia totalis with ptosis and miosis		HP:0000508	OMIM:258400	IEA					P	HPO:iea[2009-02-17]
OMIM:258400	Ophthalmoplegia totalis with ptosis and miosis		HP:0000602	OMIM:258400	IEA					P	HPO:iea[2009-02-17]
OMIM:258400	Ophthalmoplegia totalis with ptosis and miosis		HP:0000646	OMIM:258400	IEA					P	HPO:iea[2009-02-17]
OMIM:258400	Ophthalmoplegia totalis with ptosis and miosis		HP:0000007	OMIM:258400	IEA					I	HPO:iea[2009-02-17]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0003621	PMID:10966831	PCS		1/9			C	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001663	PMID:10966831	PCS		2/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0003596	PMID:10966831	PCS		4/9			C	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001695	PMID:10966831	PCS		2/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0003584	PMID:10966831	PCS		1/9			C	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001681	PMID:10330430	PCS		2/14			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0003581	PMID:10330430	PCS		3/3			C	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0002094	PMID:10966831;PMID:10330430	PCS		6/23			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0011711	PMID:10966831	PCS		1/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0011712	PMID:10966831	PCS		2/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0011713	PMID:10330430	PCS		2/14			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0031971	PMID:10330430	PCS		5/14			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001639	PMID:10966831;PMID:10330430	PCS		11/23			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0011462	PMID:10966831	PCS		3/9			C	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001635	PMID:10330430	PCS		1/14			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001712	PMID:10330430	PCS		3/14			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0004749	PMID:10330430	PCS		1/14			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0100749	PMID:10966831	PCS		2/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001962	PMID:10966831	PCS		3/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001279	PMID:10966831	PCS		2/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0001631	PMID:10966831	PCS		1/9			P	HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0000006	PMID:10330430	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11]
OMIM:612098	Cardiomyopathy, familial hypertrophic, 11		HP:0004756	PMID:10966831	PCS		1/9			P	HPO:probinson[2022-07-11]
OMIM:614402	Microphthalmia, syndromic 11		HP:0000175	PMID:22095910	PCS		1/1		HP:0012832	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-13]
OMIM:614402	Microphthalmia, syndromic 11		HP:0003577	PMID:22095910	PCS		1/1			C	HPO:probinson[2022-12-13]
OMIM:614402	Microphthalmia, syndromic 11		HP:0034396	PMID:22095910	PCS		1/1			P	HPO:probinson[2023-01-27]
OMIM:614402	Microphthalmia, syndromic 11		HP:0001274	PMID:22095910	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614402	Microphthalmia, syndromic 11		HP:0001263	PMID:22095910	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614402	Microphthalmia, syndromic 11		HP:0000007	PMID:22095910	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:614402	Microphthalmia, syndromic 11		HP:0000568	PMID:22095910	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-13]
OMIM:614402	Microphthalmia, syndromic 11		HP:0012687	PMID:22095910	PCS		1/1			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-12-13]
OMIM:614402	Microphthalmia, syndromic 11		HP:0000204	PMID:22095910	PCS		1/1		HP:0012832	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-13]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002487	PMID:17287286	PCS		12/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0003236	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000365	PMID:15877282;PMID:17287286	PCS		12/13			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002540	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000486	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0003355	OMIM:612073	TAS					P	HPO:skoehler[2013-01-22]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001332	PMID:17287286	PCS		12/12			P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0004322	PMID:17287286	PCS		8/11			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001250	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002283	PMID:15877282	PCS		1/2			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001252	PMID:15877282;PMID:17287286	PCS		14/14			P	HPO:probinson[2023-04-06];HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002020	PMID:15877282	PCS		1/2			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0003593	PMID:15877282	PCS		1/2			C	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001270	PMID:17287286	PCS		12/12			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0012469	PMID:17287286	PCS		1/12			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001508	PMID:17287286	PCS		1/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000737	PMID:15877282	PCS		1/2			P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0008972	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001349	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0008872	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000975	PMID:17287286	PCS		4/12			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002912	PMID:17287286	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0003128	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001265	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0003202	PMID:17287286	PCS		12/12			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002059	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002134	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002197	PMID:15877282	PCS		2/2			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002151	PMID:15877282;PMID:17287286	PCS		8/10			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002490	PMID:17287286	PCS		4/4			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002194	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0011344	PMID:15877282	PCS		2/2			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000407	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001518	PMID:15877282	PCS		2/2			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0012120	PMID:17287286	PCS		10/10			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000508	PMID:15877282	PCS		1/2			P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000602	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0009830	OMIM:612073	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0000007	PMID:15877282	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001935	PMID:15877282	PCS		2/2			P	HPO:probinson[2023-04-06]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002747	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002305	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0002448	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0001257	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612073	Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)		HP:0008945	OMIM:612073	IEA					P	HPO:skoehler[2010-06-19]
OMIM:619126	Immunodeficiency 75		HP:0020072	PMID:32518946	PCS		1/3			P	HPO:probinson[2021-01-07];HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0030388	PMID:32518946	PCS		3/3			P	HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0011343	PMID:32518946	PCS		3/3			P	HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0002110	PMID:32518946	PCS		3/3			P	HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:4000057	PMID:32518946	PCS		2/3			P	HPO:probinson[2021-06-13]
OMIM:619126	Immunodeficiency 75		HP:0002729	PMID:32518946	PCS					P	HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0003593	PMID:32518946	PCS		3/3			C	HPO:probinson[2021-01-24]
OMIM:619126	Immunodeficiency 75		HP:0000007	PMID:32518946	PCS					I	HPO:probinson[2021-01-07];HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0002716	PMID:32518946	PCS		3/3			P	HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0002205	PMID:32518946	PCS		3/3			P	HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0001433	PMID:32518946	PCS		3/3			P	HPO:probinson[2021-01-07]
OMIM:619126	Immunodeficiency 75		HP:0002665	PMID:32518946	PCS		3/3			P	HPO:probinson[2021-01-07]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0002510	PMID:19542079	PCS		2/2			P	HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0002650	PMID:19542079	PCS		2/2			P	HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001266	OMIM:618238	IEA		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001332	PMID:19542079	PCS	HP:0011463	2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0011968	OMIM:618238	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001250	OMIM:618238	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0002340	PMID:19542079	PCS		2/2			P	HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001260	PMID:19542079	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001274	PMID:18940309	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001263	PMID:19542079	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001290	OMIM:618238	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0002490	PMID:19542079	PCS		1/1			P	HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0011923	PMID:19542079;PMID:18940309	PCS		3/3			P	HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001508	OMIM:618238	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0000639	OMIM:618238	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0000508	OMIM:618238	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0009112	PMID:18940309	PCS	HP:0003577	1/1			P	HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0000007	PMID:18940309	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0000648	OMIM:618238	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0000846	PMID:18940309	PCS		1/1			P	HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001511	PMID:18940309	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0001257	PMID:19542079	PCS	HP:0011463	2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-07-09]
OMIM:618238	Mitochondrial complex I deficiency, nuclear type 16		HP:0003128	PMID:18940309	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-09]
OMIM:610102	C7 deficiency		HP:0005430	PMID:17407100	PCS		9/9			P	HPO:probinson[2020-08-13]
OMIM:610102	C7 deficiency		HP:0033058	PMID:17407100	PCS		9/9			P	HPO:probinson[2020-08-13]
OMIM:610102	C7 deficiency		HP:0000007	PMID:9856499	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-21]
OMIM:610102	C7 deficiency		HP:0005381	PMID:15831990	PCS					P	HPO:probinson[2013-03-31]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002465	OMIM:224050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0003577	OMIM:224050	TAS					C	HPO:skoehler[2012-10-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0000486	PMID:18326629	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0000640	OMIM:224050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0004322	OMIM:224050	IEA					P	HPO:iea[2009-02-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002365	OMIM:224050	TAS					P	HPO:skoehler[2014-04-04]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001310	OMIM:224050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001250	PMID:18326629	PCS		2/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001272	OMIM:224050	IEA					P	HPO:iea[2009-02-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002066	OMIM:224050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001252	OMIM:224050	IEA					P	HPO:iea[2009-02-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0003593	PMID:18326629	PCS		4/4			C	HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001290	OMIM:224050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002080	OMIM:224050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0000518	OMIM:224050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0007068	PMID:18326629	PCS		4/4			P	HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001302	OMIM:224050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001763	PMID:18326629	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001249	PMID:18326629	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001347	OMIM:224050	IEA					P	HPO:iea[2009-02-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002136	OMIM:224050	IEA					P	HPO:iea[2009-02-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002078	PMID:18326629	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0000750	OMIM:224050	TAS					P	HPO:skoehler[2013-06-04]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001321	PMID:18326629	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0031936	PMID:18326629	PCS		4/4			P	HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002395	PMID:18326629	PCS		4/4			P	HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001260	PMID:18326629	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0003680	OMIM:224050	IEA					C	HPO:skoehler[2010-06-19]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0001263	PMID:18326629	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0002075	OMIM:224050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0000007	PMID:16080122	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0009878	PMID:18326629	PCS		4/4			P	HPO:probinson[2023-03-11];HPO:probinson[2023-03-11]
OMIM:224050	Cerebellar hypoplasia, impaired intellectual development, and dysequilibrium syndrome 1		HP:0009879	OMIM:224050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608995	Dyslexia, susceptibility to, 8		HP:0010522	OMIM:608995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608995	Dyslexia, susceptibility to, 8		HP:0001426	OMIM:608995	IEA					I	HPO:iea[2009-02-17]
OMIM:608995	Dyslexia, susceptibility to, 8		HP:0000006	OMIM:608995	IEA					I	HPO:iea[2009-02-17]
OMIM:181440	Scheuermann disease		HP:0002808	OMIM:181440	IEA					P	HPO:skoehler[2010-06-20]
OMIM:181440	Scheuermann disease		HP:0010891	OMIM:181440	IEA					P	HPO:skoehler[2015-01-27]
OMIM:181440	Scheuermann disease		HP:0040188	OMIM:181440	IEA					P	HPO:skoehler[2018-10-08]
OMIM:181440	Scheuermann disease		HP:0000006	OMIM:181440	IEA					I	HPO:iea[2009-02-17]
OMIM:125490	Dentinogenesis imperfecta 1		HP:0006286	PMID:11175779	PCS					P	HPO:probinson[2023-03-31]
OMIM:125490	Dentinogenesis imperfecta 1		HP:0000703	PMID:11175779	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:125490	Dentinogenesis imperfecta 1		HP:0000006	PMID:11175779	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002982	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000046	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001250	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0003196	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0005495	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000280	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0030736	OMIM:269150	TAS					P	HPO:skoehler[2017-07-13]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0006392	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0011220	OMIM:269150	TAS					P	HPO:probinson[2012-05-01]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000316	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000954	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000998	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0009104	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000879	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0008897	OMIM:269150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000158	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001249	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000054	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000890	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000452	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002079	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0004492	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0011800	OMIM:269150	TAS					P	HPO:skoehler[2013-11-28]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001739	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0006387	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000329	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000047	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000006	OMIM:269150	IEA					I	HPO:skoehler[2010-06-19]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000369	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000126	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000885	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002521	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002884	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000340	OMIM:269150	TAS					P	HPO:probinson[2012-05-01]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001795	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000463	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000064	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001508	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0010034	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000935	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0009882	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000813	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002119	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000059	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002557	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0006657	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002179	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002059	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001762	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002694	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001162	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000072	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000272	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000470	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000071	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0005280	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0032075	PMID:18398855	PCS		HP:0040284			P	HPO:probinson[2019-01-16]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0009792	OMIM:269150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000348	OMIM:269150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0002645	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0000586	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:269150	Schinzel-Giedion midface-retraction syndrome		HP:0001631	OMIM:269150	IEA					P	HPO:iea[2009-02-17]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0006517	PMID:21075760	PCS	HP:0003581	1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0006517	PMID:21205713	PCS	HP:0003621	1/1			P	HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0020050	PMID:21205713	PCS		0/1			P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13];HPO:probinson[2024-03-15]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0025179	PMID:21075760	PCS	HP:0003581	1/1			P	HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0025179	PMID:21205713	PCS	HP:0003621	1/1			P	HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0002094	PMID:21205713	PCS	HP:0003621	1/1			P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0000007	PMID:21075760	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0002093	PMID:21075760	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0030879	PMID:21205713	PCS	HP:0003621	1/1			P	HPO:probinson[2020-10-13]
OMIM:614370	Surfactant metabolism dysfunction, pulmonary, 5		HP:0002875	PMID:21075760	PCS	HP:0003581	1/1			P	HPO:probinson[2020-10-13]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0001344	PMID:21744492	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0009916	PMID:21744492	PCS		2/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0002571	PMID:21744492	PCS		3/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0001419	PMID:21744492	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0011463	PMID:21744492	PCS		4/5			C	HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0001263	PMID:21744492	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0003593	PMID:21744492	PCS		1/5			C	HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0011733	PMID:21744492	PCS		0/4			P	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0001270	PMID:21744492	PCS		5/5			P	HPO:skoehler[2012-10-14]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0002119	PMID:21744492	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0001249	PMID:21744492	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:300858	Intellectual developmental disorder, X-linked syndromic 17		HP:0000522	PMID:21744492	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2024-03-09]
OMIM:606012	Deafness, autosomal dominant 18		HP:0001730	OMIM:606012	TAS					P	HPO:skoehler[2015-10-11]
OMIM:606012	Deafness, autosomal dominant 18		HP:0000006	OMIM:606012	IEA					I	HPO:skoehler[2015-10-11]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0010529	PMID:32666117	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0003596	PMID:32666117;PMID:23338750	PCS		9/12			C	HPO:probinson[2021-03-13];HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0002354	PMID:32666117;PMID:23338750	PCS		12/12			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13];HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0002145	PMID:23338750	PCS					P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0002442	PMID:32666117	PCS		2/2			P	HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0003584	PMID:32666117;PMID:23338750	PCS		2/12			C	HPO:probinson[2021-03-13];HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0002283	PMID:32666117	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0002185	PMID:23338750	PCS					P	HPO:probinson[2021-03-13]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0002381	PMID:23338750	PCS					P	HPO:probinson[2021-03-13]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0000708	PMID:23338750	PCS					P	HPO:probinson[2021-03-13]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0033051	PMID:32666117	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0000726	PMID:32666117;PMID:23338750	PCS		12/12			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13];HPO:probinson[2022-03-04]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0011462	PMID:23338750	PCS		1/10			C	HPO:probinson[2021-03-13]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0007354	PMID:23338750	PCS					P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619132	Frontotemporal dementia and/or amytrophic lateral sclerosis 8		HP:0000006	PMID:32185393	PCS					I	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0004325	PMID:25282101	PCS		17/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0003621	PMID:25282101	PCS		8/17			C	HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0004389	PMID:25282101	PCS		17/17			P	HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0001662	PMID:25282101	PCS		17/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0011704	PMID:25282101	PCS		17/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0005155	PMID:25282101	PCS		4/17			P	HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0005110	PMID:25282101	PCS		1/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0001508	PMID:25282101	PCS		17/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0031295	PMID:25282101	PCS		8/17			P	HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0011462	PMID:25282101	PCS		9/17			C	HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0001647	PMID:25282101	PCS		1/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0000007	PMID:25282101	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0004749	PMID:25282101	PCS		5/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0001642	PMID:25282101	PCS		1/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:616201	Chronic atrial and intestinal dysrhythmia		HP:0001653	PMID:25282101	PCS		3/17			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-30]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0012165	PMID:22019272	PCS					P	HPO:probinson[2013-03-12]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0001166	PMID:22019272	PCS					P	HPO:probinson[2013-03-12]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0001363	PMID:22019272	PCS					P	HPO:probinson[2013-03-12]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0030674	PMID:22019272	PCS					C	HPO:probinson[2020-07-20]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0002085	PMID:22019272	PCS					P	HPO:probinson[2013-03-12]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0000007	PMID:22019272	PCS					I	HPO:probinson[2013-01-09]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0003041	PMID:22019272	PCS					P	HPO:probinson[2013-03-12]
OMIM:614416	Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies		HP:0000248	PMID:22019272	PCS					P	HPO:probinson[2013-03-12]
OMIM:188470	Thyroid cancer, nonmedullary, 2		HP:0002895	PMID:23539728	PCS					P	HPO:probinson[2020-07-20]
OMIM:188470	Thyroid cancer, nonmedullary, 2		HP:0001442	OMIM:188470	TAS					I	HPO:skoehler[2019-02-22]
OMIM:188470	Thyroid cancer, nonmedullary, 2		HP:0040198	OMIM:188470	TAS					P	HPO:skoehler[2015-12-30]
OMIM:188470	Thyroid cancer, nonmedullary, 2		HP:0006731	OMIM:188470	TAS					P	HPO:iea[2009-02-17]
OMIM:188470	Thyroid cancer, nonmedullary, 2		HP:0000006	PMID:23539728	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-07-20]
OMIM:113650	Branchiootorenal syndrome 1		HP:0004742	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0001374	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0010628	OMIM:113650	TAS					P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0004467	PMID:19206155	PCS		12/16			P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000384	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000122	PMID:19206155	PCS		2/13			P	HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0100274	PMID:19206155	PCS		1/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0002060	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0011387	PMID:19206155	PCS		5/15			P	HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0011342	PMID:19206155	PCS		2/17			P	HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0003829	OMIM:113650	IEA					I	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0008551	PMID:19206155	PCS		2/15			P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000799	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000218	PMID:19206155	PCS		1/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000378	PMID:19206155	PCS		6/15			P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000410	PMID:19206155	PCS		4/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000113	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0004712	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0004458	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000632	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000275	OMIM:113650	TAS					P	HPO:probinson[2012-05-01]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000110	PMID:19206155	PCS		1/13			P	HPO:probinson[2013-04-13];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000175	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000076	PMID:19206155	PCS		1/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000376	PMID:19206155	PCS		1/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0007925	OMIM:113650	TAS					P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000276	OMIM:113650	TAS					P	HPO:probinson[2012-05-01]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000193	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000691	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0011094	OMIM:113650	TAS					P	HPO:skoehler[2012-10-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000407	OMIM:113650	TAS					P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0009795	PMID:19206155	PCS		11/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0009797	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0009796	PMID:19206155	PCS		4/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0008586	PMID:19206155	PCS		6/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000405	PMID:19206155	PCS		7/17			P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0009798	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0007678	OMIM:113650	TAS					P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000006	OMIM:113650	IEA					I	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0002566	OMIM:113650	IEA					P	HPO:iea[2009-02-17]
OMIM:113650	Branchiootorenal syndrome 1		HP:0000402	OMIM:113650	TAS					P	HPO:probinson[2012-04-01];HPO:probinson[2022-09-02]
OMIM:612067	Dystonia 16		HP:0003676	OMIM:612067	IEA					C	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0002067	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0002062	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0001270	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0012049	OMIM:612067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612067	Dystonia 16		HP:0100543	OMIM:612067	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:612067	Dystonia 16		HP:0011463	PMID:18243799	PCS		2/7			C	HPO:probinson[2022-10-06]
OMIM:612067	Dystonia 16		HP:0009763	OMIM:612067	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612067	Dystonia 16		HP:0007325	PMID:18243799	PCS		7/7			P	HPO:probinson[2022-10-06]
OMIM:612067	Dystonia 16		HP:0001347	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0003621	PMID:18243799	PCS		4/7			C	HPO:probinson[2022-10-06]
OMIM:612067	Dystonia 16		HP:0002015	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0001300	PMID:18243799	PCS		4/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-06]
OMIM:612067	Dystonia 16		HP:0000750	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0001288	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0002451	PMID:18243799	PCS		7/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-06]
OMIM:612067	Dystonia 16		HP:0001260	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0002174	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0012514	OMIM:612067	TAS					P	HPO:skoehler[2014-01-28]
OMIM:612067	Dystonia 16		HP:0100660	OMIM:612067	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612067	Dystonia 16		HP:0025708	PMID:18243799	PCS		1/7			C	HPO:probinson[2022-10-06]
OMIM:612067	Dystonia 16		HP:0001618	OMIM:612067	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612067	Dystonia 16		HP:0000007	OMIM:612067	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0007256	OMIM:612067;PMID:18243799	PCS		13/17			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-10-06]
OMIM:612067	Dystonia 16		HP:0002544	OMIM:612067	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612067	Dystonia 16		HP:0004305	OMIM:612067	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0003577	PMID:29936144	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000365	PMID:29936144	PCS		0/1			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0008905	PMID:28817112	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0004322	PMID:29936144	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0005474	PMID:28817112;PMID:30657919	PCS		3/3			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0003010	PMID:29936144	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000938	OMIM:616229	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000978	PMID:29936144	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0002757	PMID:29936144	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000774	PMID:30657919	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0002953	PMID:29936144	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0003026	PMID:30657919	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0003863	PMID:28817112	PCS	HP:0030674	2/2			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0003027	PMID:28817112	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0009804	PMID:29936144	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0001382	PMID:29936144	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000592	PMID:29936144	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000308	PMID:30657919	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0034198	PMID:28817112;PMID:30657919	PCS		3/3			C	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0001518	OMIM:616229	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000926	PMID:28817112;PMID:30657919	PCS		3/3			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000007	PMID:28817112	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0006640	PMID:30657919	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0006487	PMID:30657919	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0000405	OMIM:616229	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616229	Osteogenesis imperfecta, type XVI		HP:0002645	PMID:29936144	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001374	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0002021	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0003199	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0003273	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0002020	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0010049	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001607	PMID:27426733	PCS		6/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001647	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000316	PMID:27426733	PCS		18/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0040019	OMIM:617137	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001643	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0002777	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001642	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001007	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000011	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000175	PMID:27426733	PCS	HP:0003577	5/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000494	PMID:27426733	PCS		16/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000574	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000331	PMID:27426733	PCS		13/17			P	HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000293	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000294	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0003083	PMID:27426733	PCS		18/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0012385	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0010562	PMID:27426733	PCS		8/18			P	HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000407	PMID:27426733	PCS		15/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0002949	PMID:27426733	PCS		9/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000767	OMIM:617137	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000405	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000201	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000322	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000006	PMID:27426733	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000369	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0034391	PMID:27426733	PCS		18/18			P	HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001655	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0003015	PMID:27426733	PCS		13/14			P	HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0002002	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0010307	PMID:27426733	PCS		6/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0010743	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0009487	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0008872	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000218	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000455	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000377	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000336	PMID:27426733	PCS		18/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0002650	PMID:27426733	PCS		13/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0001762	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000431	PMID:27426733	PCS		18/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000193	PMID:27426733	PCS	HP:0003577	5/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000592	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0005280	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0011304	PMID:27426733	PCS		15/16			P	HPO:probinson[2022-11-22]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0100279	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000307	OMIM:617137	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000823	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000465	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617137	Frontometaphyseal dysplasia 2		HP:0000028	OMIM:617137	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:116700	Cataract 13 with adult i phenotype		HP:0000519	PMID:21912254	PCS					P	HPO:skoehler[2012-10-17]
OMIM:116700	Cataract 13 with adult i phenotype		HP:0000007	OMIM:116700	TAS					I	HPO:skoehler[2017-07-13]
OMIM:618204	Immunodeficiency 15A		HP:0031292	PMID:30337470	PCS		2/4			P	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0040154	PMID:30337470	PCS		1/4			P	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0011463	PMID:30337470	PCS					C	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0002728	PMID:30337470	PCS		1/4			P	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0030374	PMID:30337470	PCS		2/2			P	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0000403	PMID:30337470	PCS		3/4			P	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0002205	PMID:30337470	PCS		2/4			P	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0011108	PMID:30337470	PCS		2/4			P	HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0000006	PMID:30337470	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-30]
OMIM:618204	Immunodeficiency 15A		HP:0005415	PMID:30337470	PCS		2/2			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:194071	Multiple tumor-associated chromosome region 1		HP:0001442	OMIM:194071	IEA					I	HPO:iea[2009-02-17]
OMIM:194071	Multiple tumor-associated chromosome region 1		HP:0002667	OMIM:194071	IEA					P	HPO:iea[2009-02-17]
OMIM:194071	Multiple tumor-associated chromosome region 1		HP:0000006	OMIM:194071	IEA					I	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0001034	OMIM:112200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:112200	Blue rubber bleb nevus		HP:0000153	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0001891	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0002576	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0002584	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0002035	OMIM:112200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:112200	Blue rubber bleb nevus		HP:0005520	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0001392	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0002580	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0002086	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0001873	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0002756	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0000006	OMIM:112200	IEA					I	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0007129	OMIM:112200	IEA					P	HPO:iea[2009-02-17]
OMIM:112200	Blue rubber bleb nevus		HP:0001028	OMIM:112200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:184510	Steatocystoma multiplex with natal teeth		HP:0000695	OMIM:184510	IEA					P	HPO:iea[2009-02-17]
OMIM:184510	Steatocystoma multiplex with natal teeth		HP:0001597	OMIM:184510	IEA					P	HPO:iea[2009-02-17]
OMIM:184510	Steatocystoma multiplex with natal teeth		HP:0012035	OMIM:184510	IEA					P	HPO:skoehler[2015-01-27]
OMIM:184510	Steatocystoma multiplex with natal teeth		HP:0000006	OMIM:184510	IEA					I	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0000651	OMIM:273120	IEA					P	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0000639	OMIM:273120	IEA					P	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0001959	OMIM:273120	IEA					P	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0009792	OMIM:273120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:273120	Teratoma, pineal		HP:0001438	OMIM:273120	IEA					P	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0000007	OMIM:273120	IEA					I	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0000103	OMIM:273120	IEA					P	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0001269	OMIM:273120	IEA					P	HPO:iea[2009-02-17]
OMIM:273120	Teratoma, pineal		HP:0002514	OMIM:273120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0003752	PMID:38344586;PMID:36733446	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0025709	PMID:36733446	PCS		1/1			C	HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0003621	PMID:38344586	PCS		1/1			C	HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0002486	PMID:36733446	PCS		0/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0031352	PMID:38344586	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0002094	PMID:38344586	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0002900	PMID:38344586;PMID:36733446	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0003768	PMID:36733446	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2024-03-16]
OMIM:613345	Hypokalemic periodic paralysis, type 2		HP:0000006	PMID:38344586	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-16]
OMIM:602248	Malignant atrophic papulosis		HP:0002202	OMIM:602248	IEA					P	HPO:iea[2009-02-17]
OMIM:602248	Malignant atrophic papulosis		HP:0001297	PMID:19249895	PCS					P	HPO:probinson[2012-07-21]
OMIM:602248	Malignant atrophic papulosis		HP:0002563	OMIM:602248	IEA					P	HPO:iea[2009-02-17]
OMIM:602248	Malignant atrophic papulosis		HP:0005244	OMIM:602248	IEA					P	HPO:iea[2009-02-17]
OMIM:602248	Malignant atrophic papulosis		HP:0000502	OMIM:602248	IEA					P	HPO:iea[2009-02-17]
OMIM:602248	Malignant atrophic papulosis		HP:0200034	PMID:19249895	PCS					P	HPO:probinson[2012-07-21]
OMIM:602248	Malignant atrophic papulosis		HP:0002239	OMIM:602248	IEA					P	HPO:iea[2009-02-17]
OMIM:602248	Malignant atrophic papulosis		HP:0000006	OMIM:602248	TAS					I	HPO:skoehler[2012-10-17]
OMIM:104310	Alzheimer disease 2		HP:0001300	OMIM:104310	IEA					P	HPO:iea[2009-02-17]
OMIM:104310	Alzheimer disease 2		HP:0000726	OMIM:104310	IEA					P	HPO:skoehler[2010-06-20]
OMIM:104310	Alzheimer disease 2		HP:0003584	OMIM:104310	IEA					C	HPO:iea[2009-02-17]
OMIM:104310	Alzheimer disease 2		HP:0002185	OMIM:104310	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:104310	Alzheimer disease 2		HP:0002423	OMIM:104310	IEA					P	HPO:iea[2009-02-17]
OMIM:104310	Alzheimer disease 2		HP:0002511	OMIM:104310	TAS					P	HPO:probinson[2009-02-17]
OMIM:104310	Alzheimer disease 2		HP:0000006	OMIM:104310	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000286	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0007517	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001374	PMID:21699693	PCS	HP:0003577	5/15			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000563	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001058	PMID:21699693;PMID:23056730	PCS		3/16			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001373	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001252	PMID:21699693	PCS	HP:0003577	14/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001252	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000482	PMID:23056730	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000678	OMIM:225400	TAS					P	HPO:probinson[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0025019	PMID:21699693	PCS		2/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001324	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0008458	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001763	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000993	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0002751	PMID:21699693	PCS	HP:0003577	11/15			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0002751	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000098	PMID:21699693	PCS		11/15		HP:0012825	P	HPO:probinson[2012-03-16];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000494	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001382	PMID:21699693	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0002194	PMID:21699693;PMID:23056730	PCS		15/16			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0007392	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000926	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000007	PMID:21699693	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000883	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000963	OMIM:225400	TAS					P	HPO:probinson[2013-08-07];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:6000330	PMID:20301635	PCS					P	HPO:probinson[2024-02-27]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000541	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000023	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0003179	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000939	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000938	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000618	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000978	PMID:21699693	PCS		2/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0006532	OMIM:225400	TAS					P	HPO:probinson[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000977	PMID:21699693;PMID:23056730	PCS		16/16			P	HPO:probinson[2013-08-07];HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000015	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0002239	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0007502	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001788	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000974	PMID:21699693	PCS		8/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001166	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001762	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0031936	PMID:21699693	PCS		6/6			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000592	PMID:23056730	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0002093	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0034006	PMID:21699693	PCS		15/15			P	HPO:probinson[2021-10-03]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0005280	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:6000826	PMID:2504907	PCS		10/10			P	HPO:probinson[2024-08-03]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001519	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000508	PMID:23056730	PCS		1/1			P	HPO:probinson[2021-08-22]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001558	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0001635	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000545	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:225400	Ehlers-Danlos syndrome, kyphoscoliotic type, 1		HP:0000501	OMIM:225400	IEA					P	HPO:iea[2009-02-17]
OMIM:617123	Retinitis pigmentosa 76		HP:0001133	PMID:26908613	PCS		4/4			P	HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0007737	PMID:26908613	PCS		2/4			P	HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0000662	PMID:26908613	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0500087	PMID:26908613	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0030631	PMID:26908613	PCS					P	HPO:probinson[2021-05-11];HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0007663	PMID:26908613	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0000007	PMID:26908613	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0011505	PMID:26908613	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-11]
OMIM:617123	Retinitis pigmentosa 76		HP:0030329	PMID:26908613	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-11]
OMIM:309840	Modifier, X-linked, for neurofunctional defects		HP:0000707	OMIM:309840	IEA					P	HPO:iea[2009-02-17]
OMIM:309840	Modifier, X-linked, for neurofunctional defects		HP:0001417	OMIM:309840	IEA					I	HPO:iea[2009-02-17]
OMIM:607330	Lathosterolosis		HP:0000341	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000286	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0025660	PMID:17853487	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0034936	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0003577	PMID:12812989;PMID:17853487	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000343	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000463	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0003155	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0001395	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0003196	PMID:12812989;PMID:17853487	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:6000199	PMID:12812989;PMID:24142275	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2024-04-03]
OMIM:607330	Lathosterolosis		HP:0000085	PMID:17853487	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0005274	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0031964	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0009085	PMID:12812989	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000939	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000518	PMID:12812989;PMID:17853487	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0005709	PMID:12812989;PMID:17853487	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0003609	PMID:17853487	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0005608	PMID:17853487	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0001987	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0001406	PMID:17853487	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0005768	PMID:12812989;PMID:17853487	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000215	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000033	PMID:12812989	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000252	PMID:12812989;PMID:17853487	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0031956	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0001762	PMID:12812989;PMID:17853487	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0001162	PMID:12812989;PMID:17853487	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0030948	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0034198	PMID:17853487	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0002904	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000508	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000007	PMID:12812989	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0200133	PMID:12812989;PMID:17853487	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0001830	PMID:12812989;PMID:17853487	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0003316	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0004823	PMID:17853487	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:607330	Lathosterolosis		HP:0000347	PMID:12812989;PMID:17853487	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0000341	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0002069	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0002188	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0002120	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0001252	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0001274	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0003593	PMID:32395830	PCS		1/1			C	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0012301	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0033725	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0007141	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0030043	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0007366	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0002119	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0025336	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0000252	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0002650	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0002133	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0001344	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0002750	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0031936	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0001263	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0004395	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0000007	PMID:32395830	PCS					I	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0004349	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620200	Congenital disorder of glycosylation, type IIy		HP:0000248	PMID:32395830	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0001419	PMID:16055928	PCS					I	HPO:probinson[2013-01-09]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0005376	PMID:16055928	PCS					P	HPO:probinson[2013-02-16]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0005101	PMID:16055928	PCS					P	HPO:probinson[2013-02-16]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0002837	PMID:16055928	PCS					P	HPO:probinson[2013-02-16]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0011109	PMID:16055928	PCS					P	HPO:probinson[2013-02-16]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0100750	PMID:16055928	PCS					P	HPO:probinson[2013-02-16]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0000510	PMID:16055928	PCS					P	HPO:probinson[2013-02-16]
OMIM:300455	Retinitis pigmentosa, X-linked, and sinorespiratory infections, withor without deafness		HP:0000388	PMID:16055928	PCS					P	HPO:probinson[2013-02-16]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000486	PMID:29053766	PCS		4/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001332	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001695	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001371	PMID:30244176;PMID:28516161	PCS		2/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001290	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001927	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000878	PMID:28516161	PCS		1/1			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001522	PMID:30244176	PCS		1/1			C	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000311	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001765	PMID:30244176;PMID:29053766	PCS		5/5			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001188	PMID:29053766	PCS		4/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002751	PMID:30244176;PMID:29053766	PCS		2/5			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000252	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001344	PMID:29053766	PCS		3/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001263	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001181	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0008081	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0012385	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002827	PMID:29053766	PCS		1/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002827	PMID:28516161	PCS		1/1			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002827	PMID:30244176	PCS	HP:0003593	1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001537	PMID:30244176;PMID:29053766	PCS		2/5			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000007	PMID:29053766	PCS					I	HPO:probinson[2020-08-14];HPO:probinson[2022-12-03]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002304	PMID:28516161	PCS		1/1			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000400	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002987	PMID:29053766	PCS		4/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0004447	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001897	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001276	PMID:30244176;PMID:29053766	PCS		5/5			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000582	PMID:29053766	PCS		1/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000343	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000463	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000023	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0012408	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0005272	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0010501	PMID:29053766	PCS		4/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002378	PMID:29053766	PCS		4/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000395	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001561	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000750	PMID:29053766	PCS		1/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001762	PMID:28516161;PMID:29053766	PCS		2/5			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002650	PMID:28516161	PCS		1/1			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000431	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000470	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002091	PMID:28516161	PCS		1/1			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0011471	PMID:28516161	PCS		1/1			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0100678	PMID:29053766	PCS		1/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001838	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000508	PMID:29053766	PCS		2/4			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001558	PMID:30244176;PMID:28516161	PCS		2/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002804	PMID:30244176;PMID:28516161	PCS		2/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001511	PMID:28516161	PCS		1/1			P	HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000543	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0001510	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0002643	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000347	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618947	Arthrogryposis multiplex congenita 5		HP:0000269	PMID:30244176	PCS		1/1			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0031956	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0025321	PMID:28898457	PCS		1/1			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0002570	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0034048	PMID:28898457	PCS		2/2			P	HPO:probinson[2022-02-03]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0030948	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0031964	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0100512	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0100513	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0004905	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0001405	PMID:28898457	PCS		1/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0000007	PMID:28898457	PCS					I	HPO:probinson[2021-10-05];HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0006579	PMID:28898457	PCS		1/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0002028	PMID:28898457	PCS		2/2			P	HPO:probinson[2021-10-05]
OMIM:619481	Bile acid malabsorption, primary, 2		HP:0003623	PMID:28898457	PCS		2/2			C	HPO:probinson[2021-10-05]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0002014	OMIM:613812	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0031956	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0001399	PMID:9802883	PCS	HP:0003593	1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0002573	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0003155	PMID:9802883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0001394	PMID:9802883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0002240	PMID:9802883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0002570	OMIM:613812	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0012115	OMIM:613812	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0012852	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0031964	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0011985	PMID:9802883	PCS	HP:0003593	1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0034294	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0008151	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0001508	PMID:9802883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0001408	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0002904	PMID:9802883	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0000007	PMID:9802883	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0001406	OMIM:613812	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0000952	PMID:9802883	PCS	HP:0003623	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0001744	PMID:9802883	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:613812	Bile acid synthesis defect, congenital, 3		HP:0003623	PMID:9802883	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-02]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0011939	OMIM:175700	TAS					P	HPO:probinson[2024-07-22]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001177	PMID:24736735	PCS		3/51			P	HPO:iea[2010-02-23];HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0002023	PMID:24736735	PCS		0/51			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000563	PMID:24736735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000243	OMIM:175700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001250	PMID:11484201	PCS		HP:0040283			P	HPO:iea[2009-10-29];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0003074	PMID:11484201	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0010567	PMID:24736735	PCS		0/51			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0010055	PMID:15739154;PMID:24736735	PCS		16/25			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000316	PMID:24736735	PCS		18/42			P	HPO:iea[2012-04-24];HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000238	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001841	PMID:24736735	PCS		37/51			P	HPO:iea[2012-04-24];HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001007	PMID:11484201	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000494	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0002079	PMID:24736735	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001263	PMID:24736735	PCS		14/45			P	HPO:probinson[2021-02-21]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0011330	OMIM:175700	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001537	PMID:24736735	PCS		4/54			P	HPO:iea[2012-04-24];HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001459	PMID:12794692	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001539	PMID:24736735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0005616	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000047	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000006	PMID:24736735	PCS					I	HPO:iea[2012-04-24];HPO:probinson[2021-02-21]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0004303	PMID:11484201	PCS		HP:0040283			P	HPO:iea[2009-10-15]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0030799	OMIM:175700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0003577	PMID:24736735	PCS		49/49			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0002683	OMIM:175700	TAS		HP:0040283			P	HPO:sdoelken[2012-04-24]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001156	PMID:24736735	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000023	PMID:24736735;OMIM:175700	PCS		3/11			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0002164	PMID:24736735	PCS		0/51			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001274	PMID:24736735;OMIM:175700	PCS		6/22			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001627	PMID:11484201	PCS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0002119	PMID:24736735	PCS		7/15			P	HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000256	PMID:24736735	PCS		28/48			P	HPO:iea[2012-04-24];HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001363	PMID:24736735	PCS		2/55			P	HPO:iea[2012-04-24];HPO:probinson[2021-02-21]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000750	PMID:24736735	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000431	PMID:15739154	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001321	PMID:24736735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001162	PMID:24736735	PCS		26/51			P	HPO:iea[2012-04-24];HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000270	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0010059	OMIM:175700	TAS		HP:0040282			P	HPO:sdoelken[2009-10-15]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0011304	PMID:24736735;OMIM:175700	PCS		18/25			P	HPO:sdoelken[2012-04-24];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0009473	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2009-10-15];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0006042	PMID:24736735	PCS		0/51			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000348	PMID:15739154	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001836	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000268	OMIM:175700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0002007	PMID:15739154	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001830	PMID:24736735	PCS		11/51			P	HPO:iea[2009-10-15];HPO:probinson[2021-02-21];HPO:probinson[2024-03-23]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001159	PMID:24736735	PCS		32/49			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0001631	PMID:24736735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:175700	Greig cephalopolysyndactyly syndrome		HP:0000028	OMIM:175700	TAS		HP:0040283			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-23]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0000494	PMID:14556253	PCS					P	HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0000407	PMID:14556253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0000506	PMID:14556253	PCS					P	HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0003196	PMID:14556253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0009487	PMID:14556253	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0000272	PMID:14556253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0000316	PMID:14556253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0000327	PMID:14556253	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0009933	PMID:14556253	PCS					P	HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0012368	PMID:14556253	PCS					P	HPO:skoehler[2014-11-27];HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0005280	PMID:14556253	PCS					P	HPO:probinson[2023-03-29]
OMIM:122880	Craniofacial-deafness-hand syndrome		HP:0000006	PMID:8664898	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001166	PMID:31587868	PCS		8/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0002650	PMID:31587868	PCS		6/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001762	PMID:31587868	PCS		1/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000276	PMID:31587868	PCS		8/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000194	PMID:31587868	PCS		7/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001382	PMID:31587868	PCS		9/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001263	PMID:31587868	PCS		10/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001252	PMID:31587868	PCS		10/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0011800	PMID:31587868	PCS		7/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0012743	PMID:31587868	PCS		5/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0012385	PMID:31587868	PCS		4/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001519	PMID:31587868	PCS	HP:0011463	10/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001629	PMID:31587868	PCS		1/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001419	PMID:31587868	PCS					I	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000718	PMID:31587868	PCS			MALE		P	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000767	PMID:31587868	PCS		1/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0002616	PMID:31587868	PCS		1/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000768	PMID:31587868	PCS		3/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000411	PMID:31587868	PCS		8/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000322	PMID:31587868	PCS		7/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0007018	PMID:31587868	PCS			MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001653	PMID:31587868	PCS	HP:0011463	3/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0001631	PMID:31587868	PCS		1/10			P	HPO:probinson[2020-04-06]
OMIM:301039	Intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type		HP:0000028	PMID:31587868	PCS		4/10	MALE		P	HPO:probinson[2020-04-06]
OMIM:246400	Letterer-Siwe disease		HP:0001298	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0002113	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0000980	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0001051	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0002094	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0003270	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0010280	OMIM:246400	IEA					P	HPO:skoehler[2010-06-18]
OMIM:246400	Letterer-Siwe disease		HP:0000737	OMIM:246400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:246400	Letterer-Siwe disease		HP:0000924	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0001903	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0000007	OMIM:246400	IEA					I	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0001945	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0001433	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0001873	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0000952	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:246400	Letterer-Siwe disease		HP:0001875	OMIM:246400	IEA					P	HPO:iea[2009-02-17]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0001595	OMIM:242100	IEA					P	HPO:iea[2009-02-17]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0001792	OMIM:242100	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0003577	PMID:18347291;PMID:19890349	PCS		10/10			C	HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0000970	PMID:19890349	PCS		8/8			P	HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0000232	PMID:18347291	PCS		1/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0001596	OMIM:242100	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0025114	OMIM:242100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0003241	OMIM:242100	IEA					P	HPO:iea[2009-02-17]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0025092	OMIM:242100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0003470	OMIM:242100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0010783	OMIM:242100	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0009381	OMIM:242100	TAS		HP:0040283			P	HPO:skoehler[2013-01-22]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0001816	OMIM:242100	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0033252	PMID:18347291	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0007431	OMIM:242100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0000007	PMID:19890349	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0000656	PMID:18347291;PMID:19890349	PCS		7/8			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11];HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0000966	OMIM:242100	TAS		HP:0040281			P	HPO:skoehler[2013-01-22]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0007479	PMID:19890349	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0007479	PMID:18347291	PCS	HP:0003577	2/2			P	HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0001510	OMIM:242100	IEA					P	HPO:iea[2009-02-17]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0000982	PMID:19890349	PCS		6/8			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-11]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0000962	OMIM:242100	TAS					P	HPO:skoehler[2013-01-21]
OMIM:242100	Ichthyosis, congenital, autosomal recessive 2		HP:0001831	OMIM:242100	TAS		HP:0040283			P	HPO:skoehler[2013-01-22]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001331	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002323	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0003236	OMIM:615287	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0007759	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002365	PMID:23359570	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001250	PMID:23359570	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001274	PMID:23359570	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001252	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002085	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0006829	OMIM:615287	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002282	PMID:23359570	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001093	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0100565	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0007260	PMID:23359570	PCS		3/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0100307	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0000618	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002539	PMID:23359570	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001305	OMIM:615287	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0000238	OMIM:615287	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002119	PMID:23359570	PCS		4/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0000878	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0008734	PMID:23359570	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002335	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0000054	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001321	PMID:23359570	PCS		4/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001263	OMIM:615287	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0003560	OMIM:615287	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0034198	PMID:23359570	PCS		4/4			C	HPO:probinson[2022-12-11];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0000007	PMID:23359570	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0007973	PMID:23359570	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001334	PMID:23359570	PCS		3/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0000003	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0001257	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0002500	PMID:23359570	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:615287	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13		HP:0000126	OMIM:615287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0003774	PMID:16912710	PCS	HP:0003593	4/4			P	HPO:probinson[2013-02-26];HPO:probinson[2020-07-20];HPO:probinson[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0003774	PMID:21236492	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0003577	PMID:16912710;PMID:21236492	PCS		4/13			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000541	PMID:21236492	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000486	PMID:16912710	PCS		1/4			P	HPO:probinson[2013-02-26];HPO:probinson[2020-07-20]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000100	PMID:16912710	PCS	HP:0003623	4/4			P	HPO:probinson[2013-02-26];HPO:probinson[2020-07-20];HPO:probinson[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000100	PMID:21236492	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000083	PMID:21236492	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0003593	PMID:16912710;PMID:21236492	PCS		4/13			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000580	PMID:21236492	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0031266	PMID:21236492	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0012574	PMID:21236492	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000518	PMID:16912710;PMID:21236492	PCS		3/12			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000639	PMID:16912710;PMID:21236492	PCS		3/13			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2013-02-26];HPO:probinson[2020-07-20]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0011463	PMID:21236492	PCS		3/9			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0032582	PMID:21236492	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0007663	PMID:21236492	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0001967	PMID:21236492	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0001104	PMID:21236492	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000510	PMID:21236492	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000099	PMID:21236492	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0003621	PMID:21236492	PCS		2/9			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000097	PMID:16912710;PMID:21236492	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000790	PMID:21236492	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000093	PMID:16912710	PCS	HP:0003593	4/4			P	HPO:probinson[2013-02-26];HPO:probinson[2020-07-20]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000093	PMID:21236492	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000609	PMID:21236492	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000822	PMID:21236492	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000007	PMID:16912710	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000568	PMID:21236492	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:614199	Nephrotic syndrome, type 5, with or without ocular abnormalities		HP:0000545	PMID:16912710	PCS		1/4			P	HPO:probinson[2013-02-26];HPO:probinson[2020-07-20]
OMIM:166740	Osteosclerosis with ichthyosis and fractures		HP:0002982	OMIM:166740	TAS					P	HPO:probinson[2013-03-10]
OMIM:166740	Osteosclerosis with ichthyosis and fractures		HP:0002980	OMIM:166740	TAS					P	HPO:probinson[2013-03-10]
OMIM:166740	Osteosclerosis with ichthyosis and fractures		HP:0008064	OMIM:166740	IEA					P	HPO:iea[2009-02-17]
OMIM:166740	Osteosclerosis with ichthyosis and fractures		HP:0011001	OMIM:166740	IEA					P	HPO:iea[2009-02-17]
OMIM:166740	Osteosclerosis with ichthyosis and fractures		HP:0005791	OMIM:166740	IEA					P	HPO:iea[2009-02-17]
OMIM:166740	Osteosclerosis with ichthyosis and fractures		HP:0002757	OMIM:166740	IEA					P	HPO:iea[2009-02-17]
OMIM:166740	Osteosclerosis with ichthyosis and fractures		HP:0000006	OMIM:166740	IEA					I	HPO:iea[2009-02-17]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0004325	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000483	PMID:38181735	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001572	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002540	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0003112	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000486	PMID:38181735	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001332	PMID:38181735	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0004322	PMID:38181735	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000083	PMID:38181735	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002020	PMID:38181735	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0033725	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0100248	PMID:38181735	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000639	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0040131	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0010450	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0012071	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002019	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002036	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000252	PMID:38181735	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000494	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000010	PMID:38181735	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001344	PMID:38181735	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002151	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0034665	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0003083	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0008003	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000527	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0004209	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002307	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001852	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001337	PMID:38181735	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000369	PMID:38181735	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000006	PMID:38181735	PCS					I	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000126	PMID:38181735	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001336	PMID:38181735	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001276	PMID:38181735	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0003577	PMID:38181735	PCS		5/7			C	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000062	PMID:38181735	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002121	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000739	PMID:38181735	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0012450	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000338	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000733	PMID:38181735	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000219	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0030084	PMID:38181735	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000577	PMID:38181735	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002015	PMID:38181735	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002136	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002650	PMID:38181735	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000750	PMID:38181735	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002098	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002090	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0011229	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0034295	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000107	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000348	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0100716	PMID:38181735	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0007018	PMID:38181735	PCS		3/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001250	PMID:38181735	PCS		4/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002066	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001252	PMID:38181735	PCS		4/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0003273	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000716	PMID:38181735	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0011463	PMID:38181735	PCS		2/7			C	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000718	PMID:38181735	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0011220	PMID:38181735	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000717	PMID:38181735	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0003429	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0025336	PMID:38181735	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001249	PMID:38181735	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0003202	PMID:38181735	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002353	PMID:38181735	PCS		5/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0002078	PMID:38181735	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001266	PMID:38181735	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001382	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0025335	PMID:38181735	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0011968	PMID:38181735	PCS		3/7			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001260	PMID:38181735	PCS		3/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000570	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001263	PMID:38181735	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0010477	PMID:38181735	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000729	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000689	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0007874	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000565	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000325	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000445	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000687	PMID:38181735	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0032615	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001992	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000540	PMID:38181735	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000020	PMID:38181735	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0005274	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0100595	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000817	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000256	PMID:38181735	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001347	PMID:38181735	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001622	PMID:38181735	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000154	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001883	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000431	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001762	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0003542	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001882	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0031936	PMID:38181735	PCS		4/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000276	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000790	PMID:38181735	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0100633	PMID:38181735	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001518	PMID:38181735	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000821	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0001357	PMID:38181735	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000664	PMID:38181735	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0040129	PMID:38181735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621122	Paul-Chao neurodevelopmental syndrome		HP:0000028	PMID:38181735	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:600852	Retinitis pigmentosa 17		HP:0007737	PMID:15563508	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:600852	Retinitis pigmentosa 17		HP:0000662	PMID:15563508	PCS	HP:0011462				P	HPO:lccarmody[2018-10-02]
OMIM:600852	Retinitis pigmentosa 17		HP:0000551	PMID:15563508	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:600852	Retinitis pigmentosa 17		HP:0000613	PMID:15563508	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:600852	Retinitis pigmentosa 17		HP:0000510	OMIM:600852	IEA					P	HPO:iea[2009-02-17]
OMIM:600852	Retinitis pigmentosa 17		HP:0000006	OMIM:600852	IEA					I	HPO:iea[2009-02-17]
OMIM:603383	Glaucoma 1, open angle, F		HP:0007906	PMID:10037570	PCS					P	HPO:probinson[2015-05-10];HPO:probinson[2020-07-22]
OMIM:603383	Glaucoma 1, open angle, F		HP:0012108	PMID:22156576	PCS					P	HPO:probinson[2015-05-10];HPO:probinson[2020-07-22]
OMIM:603383	Glaucoma 1, open angle, F		HP:0012796	PMID:10037570	PCS					P	HPO:probinson[2015-05-10];HPO:probinson[2020-07-22]
OMIM:603383	Glaucoma 1, open angle, F		HP:0007854	PMID:10037570	PCS					P	HPO:probinson[2015-05-10];HPO:probinson[2020-07-22]
OMIM:603383	Glaucoma 1, open angle, F		HP:0000006	PMID:22156576	PCS					I	HPO:probinson[2015-05-10];HPO:probinson[2020-07-22]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002421	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0004322	PMID:22503633;PMID:23418020	PCS		8/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0005257	PMID:23418020	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000243	PMID:27874174	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0003593	PMID:28288023;PMID:22503633	PCS		4/11			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000518	PMID:23418020	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000639	PMID:28288023;PMID:22503633	PCS		10/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000510	PMID:23418020	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0007843	PMID:22503633	PCS		1/11			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000358	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000252	PMID:22503633	PCS		3/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000090	PMID:28288023	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0040022	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0005819	PMID:23418020	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0009576	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000007	PMID:22503633	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001737	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0004209	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000369	PMID:23418020;PMID:27874174	PCS		2/3			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000341	PMID:28288023;PMID:27874174	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001396	PMID:22503633	PCS		3/11			P	HPO:skoehler[2012-11-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0003577	PMID:22503633	PCS		5/10			C	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000582	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0008905	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001395	OMIM:266920	IEA					P	HPO:iea[2009-02-17]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002240	PMID:22503633	PCS		2/10			P	HPO:skoehler[2012-11-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0010306	PMID:22503633	PCS		3/8			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0009162	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002119	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000218	PMID:27874174	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002236	PMID:28288023;PMID:27874174	PCS		2/2			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0034281	PMID:22503633	PCS		10/10			P	HPO:probinson[2022-06-04]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000973	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000110	PMID:28288023	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001162	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0005487	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000073	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000193	PMID:28288023	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000470	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000191	PMID:27874174	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000107	PMID:23418020;PMID:27874174	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000348	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002007	PMID:28288023	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001433	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000347	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001831	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000286	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001250	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001252	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001251	OMIM:266920	IEA					P	HPO:iea[2009-02-17]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0011463	PMID:22503633	PCS		2/10			C	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000319	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0011220	PMID:23418020	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000316	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002612	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000158	PMID:28288023	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000556	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000572	OMIM:266920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002079	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000293	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001263	PMID:23418020;PMID:22503633	PCS		2/3			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000691	PMID:28288023	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000969	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000729	PMID:22503633	PCS		2/11			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000608	PMID:22503633	PCS		2/11			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001537	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0030151	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0007994	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000963	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000687	PMID:28288023	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0030799	PMID:22503633	PCS		1/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0003774	PMID:22503633	PCS		3/11			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0003774	PMID:23418020	PCS	HP:0003621	2/2			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0003774	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0003774	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000260	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002286	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001230	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0003090	OMIM:266920	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0010743	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0100864	OMIM:266920	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001508	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001903	OMIM:266920	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0010230	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000938	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000774	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000773	PMID:22503633;PMID:27874174	PCS		3/9			P	HPO:probinson[2022-05-28];HPO:skoehler[2012-11-18];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0009803	PMID:27874174	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000550	PMID:22503633	PCS		6/9			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000154	PMID:28288023;PMID:27874174	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001363	PMID:22503633	PCS		2/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000431	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0005565	PMID:23418020	PCS		1/2			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0005280	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0032988	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0001919	PMID:27874174	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0000822	PMID:23418020	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002209	PMID:28288023	PCS		1/1			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:266920	Short-rib thoracic dysplasia 9 with or without polydactyly		HP:0002205	PMID:22503633	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0004325	PMID:26608784	PCS		6/6			P	HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0002465	OMIM:614833	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0000252	PMID:26608784	PCS		6/6			P	HPO:skoehler[2012-11-21];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0006989	PMID:26608784	PCS	HP:0003577	1/6			P	HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0002353	PMID:22939636	PCS		2/2			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001696	PMID:22939636	PCS		0/2			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0000750	PMID:22939636	PCS					P	HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0004322	PMID:26608784	PCS		6/6			P	HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001250	PMID:22939636	PCS		4/4			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001272	PMID:22939636	PCS		1/3			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001371	PMID:26608784	PCS		2/6			P	HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001260	PMID:22939636	PCS		2/4			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0000160	OMIM:614833	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001274	PMID:26608784	PCS	HP:0003577	1/6			P	HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0000609	OMIM:614833	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001339	PMID:26608784	PCS		1/6			P	HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0000007	PMID:26608784	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0007256	PMID:22939636	PCS		2/2			P	HPO:skoehler[2015-01-04];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0000568	OMIM:614833	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0001257	PMID:22939636	PCS		1/4			P	HPO:skoehler[2012-11-18];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0000883	OMIM:614833	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0002126	PMID:26608784;PMID:22939636	PCS		4/9			P	HP:probinson[2019-03-02];HPO:skoehler[2012-11-21];HP:probinson[2019-03-02]
OMIM:614833	Microcephaly, short stature, and polymicrogyria with or without seizures		HP:0003502	OMIM:614833	IEA					P	HPO:skoehler[2019-04-18]
OMIM:602089	Hemangioma, capillary infantile		HP:0003593	PMID:18931684	PCS		2/2			C	HPO:probinson[2022-03-04]
OMIM:602089	Hemangioma, capillary infantile		HP:0005306	PMID:18931684	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602089	Hemangioma, capillary infantile		HP:0000006	PMID:18931684	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2022-03-04]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000541	PMID:25604898	PCS		11/93			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000365	PMID:25604898	PCS		32/87			P	HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0001552	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0003311	PMID:25604898;OMIM:183900	PCS		28/42			P	HPO:probinson[2021-07-02];HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0001252	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0001290	OMIM:183900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0003071	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0012368	OMIM:183900	TAS					P	HPO:skoehler[2013-10-22]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0010501	OMIM:183900	TAS					P	HPO:probinson[2012-04-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002938	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002812	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002515	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002318	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0008857	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002996	OMIM:183900	TAS					P	HPO:probinson[2012-04-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002655	PMID:25604898	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000175	PMID:25604898	PCS	HP:0003621	20/93			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0003467	PMID:25604898	PCS		5/32			P	HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002650	PMID:25604898	PCS		52/93			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0001762	PMID:25604898	PCS		8/93			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0003300	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002098	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000193	PMID:25604898	PCS		2/93			P	HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000272	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000470	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002091	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002829	PMID:25604898	PCS	HP:0003621	82/93			P	HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0008142	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002808	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0002827	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000926	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0007773	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000768	OMIM:183900	IEA					P	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0008800	OMIM:183900	TAS					P	HPO:probinson[2012-04-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0008788	OMIM:183900	TAS					P	HPO:probinson[2012-05-05]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000201	PMID:25604898	PCS		13/93			P	HPO:probinson[2021-07-02]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000006	OMIM:183900	IEA					I	HPO:iea[2009-02-17]
OMIM:183900	Spondyloepiphyseal dysplasia congenita		HP:0000545	PMID:25604898	PCS		42/93			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:170650	Periodontitis, aggressive, 1		HP:0000166	PMID:10662808	PCS	HP:0003593	4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:170650	Periodontitis, aggressive, 1		HP:0006480	PMID:10662808	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:170650	Periodontitis, aggressive, 1		HP:0000007	PMID:10662808	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:170650	Periodontitis, aggressive, 1		HP:0030816	PMID:10662808	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-02]
OMIM:170650	Periodontitis, aggressive, 1		HP:0000972	PMID:10662808	PCS		0/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:620228	Retinitis pigmentosa 96, autosomal dominant		HP:0001133	PMID:28549094	PCS		14/16			P	HPO:probinson[2023-06-11]
OMIM:620228	Retinitis pigmentosa 96, autosomal dominant		HP:0007737	PMID:28549094	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620228	Retinitis pigmentosa 96, autosomal dominant		HP:0007663	PMID:28549094	PCS		17/18			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620228	Retinitis pigmentosa 96, autosomal dominant		HP:0000510	PMID:28549094	PCS		18/18			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620228	Retinitis pigmentosa 96, autosomal dominant		HP:0030329	PMID:28549094	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620228	Retinitis pigmentosa 96, autosomal dominant		HP:0000006	PMID:28549094	PCS					I	HPO:probinson[2023-06-11]
OMIM:615293	Myofibromatosis, infantile 2		HP:0020135	PMID:23731542	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-07]
OMIM:615293	Myofibromatosis, infantile 2		HP:0000006	PMID:23731542	PCS					I	HPO:skoehler[2013-08-18];HPO:probinson[2019-09-07]
OMIM:188100	Thumb deformity		HP:0009601	OMIM:188100	IEA					P	HPO:iea[2009-02-17]
OMIM:188100	Thumb deformity		HP:0001626	OMIM:188100	IEA					P	HPO:iea[2009-02-17]
OMIM:188100	Thumb deformity		HP:0000006	OMIM:188100	IEA					I	HPO:iea[2009-02-17]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0002223	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0002212	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0003477	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0002213	OMIM:615278	TAS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000463	OMIM:615278	TAS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0001263	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000280	OMIM:615278	TAS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0008070	OMIM:615278	TAS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000508	OMIM:615278	TAS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000337	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000218	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000006	PMID:21797849	PCS					I	HPO:probinson[2013-01-12]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000545	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0001634	PMID:21797849	PCS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000358	OMIM:615278	TAS					P	HPO:probinson[2014-01-05]
OMIM:615278	Cardiofaciocutaneous syndrome 2		HP:0000369	OMIM:615278	TAS					P	HPO:probinson[2014-01-05]
OMIM:141300	Hemifacial atrophy, progressive		HP:0003621	OMIM:141300	TAS					C	HPO:probinson[2022-09-04]
OMIM:141300	Hemifacial atrophy, progressive		HP:0000684	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0002232	OMIM:141300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0002277	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0002076	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0001250	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0000490	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0000581	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0001251	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0002290	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0100661	OMIM:141300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0012473	OMIM:141300	TAS					P	HPO:skoehler[2015-12-30]
OMIM:141300	Hemifacial atrophy, progressive		HP:0011331	OMIM:141300	TAS					P	HPO:skoehler[2015-01-21]
OMIM:141300	Hemifacial atrophy, progressive		HP:0002808	OMIM:141300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:141300	Hemifacial atrophy, progressive		HP:0011462	OMIM:141300	TAS					C	HPO:probinson[2022-09-04]
OMIM:141300	Hemifacial atrophy, progressive		HP:0008551	OMIM:141300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0000689	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0003778	OMIM:141300	IEA					P	HPO:iea[2009-02-17]
OMIM:141300	Hemifacial atrophy, progressive		HP:0003745	OMIM:141300	IEA					I	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0002353	OMIM:300496	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0005324	OMIM:300496	TAS					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0000750	OMIM:300496	IEA					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0002332	OMIM:300496	IEA					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0001250	OMIM:300496	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0003144	OMIM:300496	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0011463	OMIM:300496	IEA					C	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0000717	OMIM:300496	TAS					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0000723	OMIM:300496	TAS					P	HPO:skoehler[2013-06-04]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0000733	OMIM:300496	TAS					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0000758	OMIM:300496	IEA					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0001417	OMIM:300496	IEA					I	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0000721	OMIM:300496	IEA					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0001249	OMIM:300496	IEA					P	HPO:iea[2009-02-17]
OMIM:300496	Autism susceptibility, X-linked 3		HP:0000732	OMIM:300496	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000252	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000494	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000365	OMIM:301950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0004322	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0001328	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0002705	OMIM:301950	TAS					P	HPO:skoehler[2015-12-30]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000218	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0001417	OMIM:301950	IEA					I	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000411	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000465	OMIM:301950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0001642	OMIM:301950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000028	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:301950	Branchial arch syndrome, X-linked		HP:0000369	OMIM:301950	IEA					P	HPO:iea[2009-02-17]
OMIM:193520	Watson syndrome		HP:0001067	OMIM:193520	IEA					P	HPO:iea[2009-02-17]
OMIM:193520	Watson syndrome		HP:0000286	PMID:8317503	PCS		2/3			P	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0003577	PMID:8317503	PCS		3/3			C	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0004322	OMIM:193520	IEA					P	HPO:iea[2009-02-17]
OMIM:193520	Watson syndrome		HP:0004482	OMIM:193520	IEA					P	HPO:iea[2009-02-17]
OMIM:193520	Watson syndrome		HP:0011343	PMID:8317503	PCS		2/3			P	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0000316	PMID:8317503	PCS		2/3			P	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0000997	PMID:8317503	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0007565	PMID:8317503	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0030052	PMID:8317503	PCS		1/3			P	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0000768	PMID:8317503	PCS		2/3			P	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0001642	PMID:8317503	PCS		1/3			P	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0000006	PMID:8317503	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0009737	PMID:8317503	PCS		0/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0000358	PMID:8317503	PCS		3/3			P	HPO:probinson[2022-04-24]
OMIM:193520	Watson syndrome		HP:0000369	PMID:8317503	PCS		3/3			P	HPO:probinson[2022-04-24]
OMIM:619324	Hypertriglyceridemia 2		HP:0002155	PMID:26427795	PCS		2/2			P	HPO:probinson[2021-08-19]
OMIM:619324	Hypertriglyceridemia 2		HP:0003233	PMID:26427795	PCS		2/2			P	HPO:probinson[2021-08-19]
OMIM:619324	Hypertriglyceridemia 2		HP:0003124	PMID:26427795	PCS		2/2			P	HPO:probinson[2021-08-19]
OMIM:619324	Hypertriglyceridemia 2		HP:0000006	PMID:26427795	PCS					I	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:264110	Prolactin deficiency, isolated		HP:0000858	OMIM:264110	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:264110	Prolactin deficiency, isolated		HP:0000789	OMIM:264110	TAS					P	HPO:skoehler[2010-06-20]
OMIM:264110	Prolactin deficiency, isolated		HP:0008202	OMIM:264110	TAS					P	HPO:probinson[2009-02-17]
OMIM:264110	Prolactin deficiency, isolated		HP:0000007	OMIM:264110	TAS					I	HPO:probinson[2009-02-17]
OMIM:108700	Ataxia with fasciculations		HP:0001251	OMIM:108700	IEA					P	HPO:iea[2009-02-17]
OMIM:108700	Ataxia with fasciculations		HP:0002380	OMIM:108700	IEA					P	HPO:iea[2009-02-17]
OMIM:108700	Ataxia with fasciculations		HP:0000006	OMIM:108700	IEA					I	HPO:iea[2009-02-17]
OMIM:236130	HOMOCARNOSINOSIS		HP:0007703	OMIM:236130	TAS					P	HPO:skoehler[2009-02-17]
OMIM:236130	HOMOCARNOSINOSIS		HP:0001000	OMIM:236130	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236130	HOMOCARNOSINOSIS		HP:0003167	PMID:3736769	PCS					P	HPO:probinson[2009-02-17]
OMIM:236130	HOMOCARNOSINOSIS		HP:0000007	OMIM:236130	IEA					I	HPO:iea[2009-02-17]
OMIM:236130	HOMOCARNOSINOSIS		HP:0001258	OMIM:236130	IEA					P	HPO:iea[2009-02-17]
OMIM:236130	HOMOCARNOSINOSIS		HP:0001249	OMIM:236130	IEA					P	HPO:iea[2009-02-17]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0002047	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0003236	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0003201	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0003256	OMIM:145600	IEA					P	HPO:iea[2009-02-17]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0002153	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0002063	PMID:16163667	PCS				HP:0500261	P	HPO:skoehler[2013-03-27];HPO:probinson[2021-09-18]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0002905	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0002913	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0001649	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0002615	PMID:9497245	PCS				HP:0500261	P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0005967	OMIM:145600	IEA				HP:0500261	P	HPO:iea[2009-02-17]
OMIM:145600	Malignant hyperthermia, susceptibility to, 1		HP:0000006	PMID:9497245	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:614614	Deafness, autosomal dominant 4B		HP:0003621	PMID:21368133	PCS		10/10			C	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:614614	Deafness, autosomal dominant 4B		HP:0001751	PMID:21368133	PCS		0/10			P	HPO:probinson[2023-02-10]
OMIM:614614	Deafness, autosomal dominant 4B		HP:0000407	PMID:21368133	PCS		10/10			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:614614	Deafness, autosomal dominant 4B		HP:0000505	PMID:21368133	PCS		0/10			P	HPO:probinson[2023-02-10]
OMIM:614614	Deafness, autosomal dominant 4B		HP:0000006	PMID:21368133	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:308960	Leukemia, acute, ?x-linked		HP:0002488	OMIM:308960	IEA					P	HPO:iea[2009-02-17]
OMIM:308960	Leukemia, acute, ?x-linked		HP:0001417	OMIM:308960	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000486	PMID:30905399	PCS		4/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001250	PMID:30905399	PCS		2/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001274	PMID:30905399	PCS		3/8			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001290	PMID:30905399	PCS					P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0004383	PMID:30905399	PCS		1/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001270	PMID:30905399	PCS					P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001629	PMID:30905399	PCS		3/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0008872	PMID:30905399	PCS					P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001249	PMID:30905399	PCS		11/11			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001545	PMID:30905399	PCS		1/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001288	PMID:30905399	PCS					P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0002572	PMID:30905399	PCS		2/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0004792	PMID:30905399	PCS		1/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001680	PMID:30905399	PCS		1/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000407	PMID:30905399	PCS		3/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000729	PMID:30905399	PCS		5/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0011330	PMID:30905399	PCS		1/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000508	PMID:30905399	PCS		2/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001999	PMID:30905399	PCS		11/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001636	PMID:30905399	PCS		1/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000505	PMID:30905399	PCS		2/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0007018	PMID:30905399	PCS		4/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000006	PMID:30905399	PCS					I	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000545	PMID:30905399	PCS		6/12			P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0000028	PMID:30905399	PCS		1/7	MALE		P	HPO:probinson[2020-04-29]
OMIM:618748	Intellectual developmental disorder with hypotonia and behavioral abnormalities		HP:0001655	PMID:30905399	PCS		1/12			P	HPO:probinson[2020-04-29]
OMIM:614172	Immunodeficiency 21		HP:0012312	PMID:22996659;OMIM:614172	PCS		11/11			P	HPO:probinson[2023-02-11];HPO:probinson[2013-08-10]
OMIM:614172	Immunodeficiency 21		HP:0012324	OMIM:614172	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614172	Immunodeficiency 21		HP:0010976	PMID:22996659	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0025709	PMID:22996659	PCS		1/1			C	HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0001915	OMIM:614172	TAS		HP:0040283			P	HPO:skoehler[2014-04-13]
OMIM:614172	Immunodeficiency 21		HP:0001903	PMID:22996659	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0011275	OMIM:614172	TAS					P	HPO:probinson[2013-08-10]
OMIM:614172	Immunodeficiency 21		HP:0032242	PMID:22996659	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0031385	PMID:22996659	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0001888	OMIM:614172	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614172	Immunodeficiency 21		HP:0004429	OMIM:614172	TAS					P	HPO:probinson[2013-08-10]
OMIM:614172	Immunodeficiency 21		HP:0000006	PMID:21670465	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0002841	OMIM:614172	TAS					P	HPO:probinson[2013-08-10]
OMIM:614172	Immunodeficiency 21		HP:0002863	PMID:22996659	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0001875	PMID:22996659	PCS		1/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0002721	PMID:22996659	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0002754	PMID:22996659	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:614172	Immunodeficiency 21		HP:0040218	PMID:22996659	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:611022	Deafness, autosomal recessive, 24		HP:0003593	OMIM:611022	TAS					C	HPO:probinson[2009-02-17]
OMIM:611022	Deafness, autosomal recessive, 24		HP:0000007	OMIM:611022	TAS					I	HPO:probinson[2009-02-17]
OMIM:611022	Deafness, autosomal recessive, 24		HP:0011476	OMIM:611022	TAS					P	HPO:probinson[2012-07-18]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0008936	PMID:30929742	PCS	HP:0003577	5/5			P	HPO:probinson[2020-04-22];HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0002353	PMID:30929742	PCS		5/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0002540	PMID:30929742	PCS		3/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0001332	PMID:30929742	PCS		1/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0002079	PMID:30929742	PCS		1/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0001263	PMID:30929742	PCS		5/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0003593	PMID:30929742	PCS					C	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0002072	PMID:30929742	PCS		2/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0000708	PMID:30929742	PCS		3/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0100704	PMID:30929742	PCS		3/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0032660	PMID:30929742	PCS		1/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0000729	PMID:30929742	PCS		5/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0100716	PMID:30929742	PCS		1/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0012171	PMID:30929742	PCS		4/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0007359	PMID:30929742	PCS		2/5			P	HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0000006	PMID:30929742	PCS					I	HPO:probinson[2020-04-22];HPO:probinson[2020-04-22]
OMIM:618760	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements		HP:0001249	PMID:30929742	PCS		5/5			P	HPO:probinson[2020-04-22]
OMIM:615244	Nephrotic syndrome, type 8		HP:0003774	PMID:23434736	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:615244	Nephrotic syndrome, type 8		HP:0000100	PMID:23434736	PCS		2/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-03-19]
OMIM:615244	Nephrotic syndrome, type 8		HP:0001250	OMIM:615244	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615244	Nephrotic syndrome, type 8		HP:0003073	PMID:23434736	PCS		2/2			P	HPO:skoehler[2013-05-31]
OMIM:615244	Nephrotic syndrome, type 8		HP:0000093	PMID:23434736	PCS		2/2			P	HPO:skoehler[2013-05-31]
OMIM:615244	Nephrotic syndrome, type 8		HP:0012577	OMIM:615244	TAS					P	HPO:probinson[2014-01-18]
OMIM:615244	Nephrotic syndrome, type 8		HP:0012622	OMIM:615244	TAS					P	HPO:skoehler[2014-01-18]
OMIM:615244	Nephrotic syndrome, type 8		HP:0000969	OMIM:615244	TAS					P	HPO:skoehler[2013-05-31]
OMIM:615244	Nephrotic syndrome, type 8		HP:0100704	OMIM:615244	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615244	Nephrotic syndrome, type 8		HP:0000407	OMIM:615244	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615244	Nephrotic syndrome, type 8		HP:0007430	PMID:23434736	PCS		1/2			P	HPO:probinson[2023-03-19]
OMIM:615244	Nephrotic syndrome, type 8		HP:0000007	PMID:23434736	PCS					I	HPO:skoehler[2013-05-31];HPO:probinson[2023-03-19]
OMIM:615244	Nephrotic syndrome, type 8		HP:0001967	PMID:23434736	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-03-19]
OMIM:615244	Nephrotic syndrome, type 8		HP:0001249	OMIM:615244	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615244	Nephrotic syndrome, type 8		HP:0003623	PMID:23434736	PCS		2/2			C	HPO:skoehler[2013-05-31]
OMIM:615244	Nephrotic syndrome, type 8		HP:0003678	PMID:23434736	PCS					C	HPO:skoehler[2013-05-31];HPO:probinson[2023-03-19]
OMIM:277150	Van bogaert-hozay syndrome		HP:0001595	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0000483	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0000692	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0009771	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0005033	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0000007	OMIM:277150	IEA					I	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0000377	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0005280	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0000347	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:277150	Van bogaert-hozay syndrome		HP:0000545	OMIM:277150	IEA					P	HPO:iea[2009-02-17]
OMIM:615522	Cole disease		HP:0001595	PMID:25065726	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-15]
OMIM:615522	Cole disease		HP:0000164	PMID:25065726	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-15]
OMIM:615522	Cole disease		HP:0003577	PMID:24075184	PCS		1/8			C	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0001597	PMID:25065726	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-15]
OMIM:615522	Cole disease		HP:0020073	PMID:24075184;PMID:25065726	PCS		9/9			P	HPO:probinson[2022-12-13];HPO:probinson[2024-03-15]
OMIM:615522	Cole disease		HP:0025114	PMID:24075184	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0025520	PMID:24075184	PCS		2/8			P	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0003593	PMID:24075184;PMID:25065726	PCS		5/9			C	HPO:probinson[2022-12-13];HPO:probinson[2024-03-15]
OMIM:615522	Cole disease		HP:0025092	PMID:24075184	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0003074	PMID:24075184	PCS		0/4			P	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0040162	PMID:24075184	PCS					P	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0010766	PMID:24075184	PCS		4/8			P	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0011463	PMID:24075184	PCS		3/8			C	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0045059	PMID:25065726	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:615522	Cole disease		HP:0007530	PMID:24075184	PCS		8/8			P	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0100529	PMID:24075184	PCS		0/4			P	HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0000982	PMID:24075184	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0000006	PMID:24075184	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-13]
OMIM:615522	Cole disease		HP:0000962	OMIM:615522	TAS					P	HPO:skoehler[2014-01-28]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001250	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002066	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001271	PMID:10682309	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001252	PMID:10682309	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0000020	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0011463	PMID:8554069	PCS		1/1			C	HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002518	OMIM:249900	PCS					P	HPO:probinson[2012-04-11]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001324	PMID:10682309	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001268	OMIM:249900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0007305	OMIM:249900	PCS					P	HPO:probinson[2012-04-11]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001347	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001265	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002333	PMID:10682309	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002015	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0003487	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002376	PMID:8554069	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001260	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001263	PMID:8554069	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002371	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0001285	OMIM:249900	IEA					P	HPO:iea[2009-02-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0011096	PMID:8554069;PMID:10682309	PCS		2/2			P	HPO:probinson[2023-04-21];HPO:skoehler[2012-10-17]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0009830	PMID:8554069	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0000007	PMID:8554069	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002922	PMID:8554069	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0002505	PMID:8554069	PCS		1/1			P	HPO:probinson[2023-04-21]
OMIM:249900	Metachromatic leukodystrophy due to saposin B deficiency		HP:0000762	PMID:8554069;PMID:10682309	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-21];HPO:probinson[2023-04-21]
OMIM:312910	Spastic paraparesis and deafness		HP:0003621	OMIM:312910	TAS					C	HPO:probinson[2012-07-19]
OMIM:312910	Spastic paraparesis and deafness		HP:0000365	OMIM:312910	IEA					P	HPO:iea[2009-02-17]
OMIM:312910	Spastic paraparesis and deafness		HP:0004322	OMIM:312910	IEA					P	HPO:iea[2009-02-17]
OMIM:312910	Spastic paraparesis and deafness		HP:0000518	OMIM:312910	IEA					P	HPO:iea[2009-02-17]
OMIM:312910	Spastic paraparesis and deafness		HP:0001417	OMIM:312910	IEA					I	HPO:iea[2009-02-17]
OMIM:312910	Spastic paraparesis and deafness		HP:0000135	OMIM:312910	IEA					P	HPO:iea[2009-02-17]
OMIM:312910	Spastic paraparesis and deafness		HP:0001337	OMIM:312910	IEA					P	HPO:iea[2009-02-17]
OMIM:312910	Spastic paraparesis and deafness		HP:0002313	OMIM:312910	IEA					P	HPO:iea[2009-02-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0002421	PMID:15121789	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0003236	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0007957	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0003577	PMID:15121789	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000541	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0002365	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0006829	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001274	PMID:15121789	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0031882	PMID:15121789	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001270	OMIM:613153	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0012110	PMID:15121789	PCS		1/1			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0007260	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000518	OMIM:613153	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000238	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001305	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0002119	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001302	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0002335	PMID:15121789	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001265	OMIM:613153	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001321	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0011968	PMID:15121789	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0003560	PMID:15121789	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000294	PMID:15121789	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0002350	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0002093	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0003819	PMID:15121789	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0007033	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001339	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000568	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0001712	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000007	PMID:15121789	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000545	OMIM:613153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0000589	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0002500	PMID:15121789	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-27]
OMIM:613153	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5		HP:0009879	PMID:15121789	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0001254	OMIM:600649	IEA					P	HPO:iea[2009-02-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0003236	PMID:8651281	PCS		1/1			P	HPO:probinson[2012-03-18];HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0002013	OMIM:600649	IEA					P	HPO:iea[2009-02-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0001640	PMID:8651281	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0001250	OMIM:600649	IEA					P	HPO:iea[2009-02-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0003593	OMIM:600649	PCS					C	HPO:probinson[2012-03-18]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0002240	PMID:8651281	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0001987	OMIM:600649	IEA					P	HPO:iea[2009-02-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0000007	PMID:8651281	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0025435	PMID:8651281	PCS		1/1			P	HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0002910	PMID:1999498	PCS					P	HPO:probinson[2012-03-18]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0004756	PMID:8651281	PCS		1/1			P	HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0001403	OMIM:600649	IEA					P	HPO:iea[2009-02-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0005943	PMID:8651281	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0001985	PMID:8651281	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-17]
OMIM:600649	Carnitine palmitoyltransferase II deficiency, infantile		HP:0001644	OMIM:600649	IEA					P	HPO:iea[2009-02-17]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0002521	PMID:29215095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0003676	PMID:29215095	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0002540	PMID:29215095	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0000463	PMID:29215095	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001272	PMID:29215095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001371	PMID:29215095	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001250	PMID:29215095	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0003593	PMID:29215095	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0012471	PMID:29215095	PCS		2/4			P	HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0009765	PMID:29215095	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001522	PMID:29215095	PCS		1/4			C	HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0000212	PMID:29215095	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0002415	PMID:29215095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001007	PMID:29215095	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001347	PMID:29215095	PCS		4/4			P	HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0002751	PMID:29215095	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0002059	PMID:29215095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0000252	PMID:29215095	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001344	PMID:29215095	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0002079	PMID:29215095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0011968	PMID:29215095	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0012736	PMID:29215095	PCS		4/4			P	HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0000007	PMID:29215095	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0001510	PMID:29215095	PCS		4/4			P	HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0000303	PMID:29215095	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:618006	Leukodystrophy, hypomyelinating, 17		HP:0000687	PMID:29215095	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0000252	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0003577	PMID:32885237	PCS		5/5			C	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0002023	PMID:32885237	PCS		2/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0004322	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0004320	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0001263	PMID:32885237	PCS		3/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0000085	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0011480	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0001618	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0000729	PMID:32885237	PCS		2/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0002937	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0001647	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0000007	PMID:32885237	PCS					I	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0008751	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0007687	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0009765	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0007633	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0000960	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0000589	PMID:32885237	PCS		4/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0001007	PMID:32885237	PCS		1/5			P	HPO:probinson[2021-07-06]
OMIM:619318	Oculogastrointestinal neurodevelopmental syndrome		HP:0020206	PMID:32885237	PCS		2/5			P	HPO:probinson[2021-07-06]
OMIM:204800	AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF		HP:0001939	OMIM:204800	IEA					P	HPO:iea[2009-02-17]
OMIM:204800	AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF		HP:0000007	OMIM:204800	IEA					I	HPO:iea[2009-02-17]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0002069	PMID:29668857	PCS		4/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0002521	OMIM:618012	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0002540	PMID:29668857	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0000540	OMIM:618012	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001272	PMID:29668857	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001252	PMID:29668857	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0003593	PMID:29668857	PCS		3/4			C	HPO:probinson[2023-05-09];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0032794	PMID:29668857	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0012469	PMID:29668857	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0011463	PMID:29668857	PCS		1/4			C	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0000612	PMID:29668857	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0020221	PMID:29668857	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0003429	PMID:29668857	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001249	PMID:29668857	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001347	OMIM:618012	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0002059	PMID:29668857	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0000252	PMID:29668857	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001344	PMID:29668857	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0031936	OMIM:618012	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001288	OMIM:618012	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0002079	OMIM:618012	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0002373	PMID:29668857	PCS		4/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001263	PMID:29668857	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0001285	PMID:29668857	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0032792	PMID:29668857	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0200134	PMID:29668857	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0000648	PMID:29668857	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0007359	PMID:29668857	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:618012	Developmental and epileptic encephalopathy 93		HP:0000006	PMID:29668857	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-09]
OMIM:617321	Yao syndrome		HP:0002014	PMID:27984003	PCS		34/52			P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0003565	PMID:27984003	PCS		14/48			P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0002102	PMID:27984003	PCS					P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0000155	PMID:27984003	PCS		14/52			P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0002099	PMID:27984003	PCS					P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0001097	PMID:23102769	PCS		9/22			P	HP:probinson[2018-07-05];HPO:probinson[2024-03-15]
OMIM:617321	Yao syndrome		HP:0002829	PMID:27984003	PCS					P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0011123	PMID:23102769;PMID:27984003	PCS		29/32			P	HP:probinson[2018-07-05];HPO:probinson[2024-03-15]
OMIM:617321	Yao syndrome		HP:0000217	PMID:27984003	PCS					P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0001954	PMID:23102769;PMID:27984003	PCS		48/74			P	HP:probinson[2018-07-05];HPO:probinson[2024-03-15]
OMIM:617321	Yao syndrome		HP:0001426	PMID:27984003	PCS					I	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0001701	PMID:27984003	PCS					P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0100749	PMID:23102769;PMID:27984003	PCS		12/74			P	HP:probinson[2018-07-05];HPO:probinson[2024-03-15]
OMIM:617321	Yao syndrome		HP:0000988	PMID:26070941	PCS		49/54			P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0001714	PMID:27984003	PCS					P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0001824	PMID:23102769;PMID:27984003	PCS		35/76			P	HP:probinson[2018-07-05];HPO:probinson[2024-03-15]
OMIM:617321	Yao syndrome		HP:0000554	PMID:23102769	PCS		0/22			P	HP:probinson[2018-07-05];HPO:probinson[2024-03-15]
OMIM:617321	Yao syndrome		HP:0002027	PMID:27984003	PCS		34/52			P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0000787	PMID:27984003	PCS					P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0003326	PMID:26070941	PCS		19/54			P	HP:probinson[2018-07-05]
OMIM:617321	Yao syndrome		HP:0001369	PMID:27984003	PCS		41/52			P	HP:probinson[2018-07-05]
OMIM:601543	Deafness, autosomal dominant nonsyndromic sensorineural 12		HP:0000407	OMIM:601543	TAS					P	HPO:skoehler[2010-06-18]
OMIM:601543	Deafness, autosomal dominant nonsyndromic sensorineural 12		HP:0000006	OMIM:601543	IEA					I	HPO:iea[2009-02-17]
OMIM:614628	Keratoconus 8		HP:0000563	OMIM:614628	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614628	Keratoconus 8		HP:0000006	OMIM:614628	TAS					I	HPO:skoehler[2012-10-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0001144	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000175	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0001374	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0001596	OMIM:164180	IEA					P	HPO:skoehler[2010-06-20]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0002079	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0001250	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0001274	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0002282	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0003191	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000639	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000528	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000568	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0001305	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0007510	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000625	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0007115	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0003745	OMIM:164180	IEA					I	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000028	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000765	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0001249	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:164180	Oculocerebrocutaneous syndrome		HP:0000324	OMIM:164180	IEA					P	HPO:iea[2009-02-17]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0003124	OMIM:144250	IEA					P	HPO:skoehler[2019-09-07]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0003077	OMIM:144250	IEA					P	HPO:skoehler[2019-09-07]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0003141	PMID:4718953	PCS					P	HPO:probinson[2017-08-27]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0003362	PMID:4718953	PCS					P	HPO:probinson[2017-08-27]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0001658	PMID:4718953	PCS					P	HPO:iea[2009-02-17]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0001114	OMIM:144250	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0031798	PMID:9373757	PCS					P	HPO:probinson[2018-03-04]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0000006	OMIM:144250	TAS					I	HPO:iea[2009-02-17]
OMIM:144250	Hyperlipidemia, familial combined, 3		HP:0031800	PMID:12738753	PCS					P	HPO:probinson[2018-03-04]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0003577	PMID:1356229	PCS		3/3			C	HPO:probinson[2022-04-18]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0000021	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0004322	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0002013	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0001250	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0001508	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0001959	OMIM:304800	IEA		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0000737	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0001419	PMID:1356229	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0001955	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0008872	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0000873	PMID:1356229	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-04-18]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0003228	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0000103	OMIM:304800	IEA		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0002019	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0001986	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0001249	OMIM:304800	IEA					P	HPO:iea[2009-02-17]
OMIM:304800	Diabetes insipidus, nephrogenic, X-linked		HP:0003623	OMIM:304800	IEA					C	HPO:iea[2009-02-17]
OMIM:618774	CEBALID syndrome		HP:0000341	PMID:31834374	PCS					P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000365	PMID:31834374	PCS		16/20			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000486	PMID:31834374	PCS					P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000463	PMID:31839203;PMID:31834374	PCS		24/25			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0002167	PMID:31839203	PCS		3/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0001250	PMID:31834374	PCS		6/21			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000262	PMID:31834374	PCS					P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0003196	PMID:31839203	PCS		3/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0001290	PMID:31839203;PMID:31834374	PCS		19/21			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0001270	PMID:31834374	PCS		19/20			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0012368	PMID:31839203	PCS		3/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000639	PMID:31834374	PCS					P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0033011	PMID:31839203	PCS		1/3			P	HPO:probinson[2020-06-09]
OMIM:618774	CEBALID syndrome		HP:0011220	PMID:31839203	PCS		2/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000316	PMID:31839203;PMID:31834374	PCS		22/24			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000218	PMID:31834374	PCS		15/21			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000377	PMID:31834374	PCS		22/22			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0009921	PMID:31834374	PCS					P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0001249	PMID:31834374	PCS		16/17			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000776	PMID:31834374	PCS		2/21			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000358	PMID:31839203	PCS		2/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000457	PMID:31839203	PCS		2/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0002553	PMID:31839203	PCS		2/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000494	PMID:31834374	PCS		15/21			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000750	PMID:31834374	PCS		18/20			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000574	PMID:31839203	PCS		3/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0011968	PMID:31839203;PMID:31834374	PCS		14/21			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0002591	PMID:31839203	PCS	HP:0003593	3/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0011800	PMID:31834374	PCS		21/22			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0011344	PMID:31839203	IEA	HP:0003593	3/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0005280	PMID:31839203	PCS		2/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0001357	PMID:31834374	PCS					P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000268	PMID:31839203;PMID:31834374	PCS		12/13			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000006	PMID:31834374	PCS					I	HPO:probinson[2020-05-09];HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000248	PMID:31834374	PCS					P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0000369	PMID:31839203	PCS		3/3			P	HPO:probinson[2020-05-09]
OMIM:618774	CEBALID syndrome		HP:0002126	PMID:31839203	PCS		2/3			P	HPO:probinson[2020-05-09]
OMIM:109350	Gastroesophageal reflux		HP:0100633	OMIM:109350	TAS					P	HPO:skoehler[2012-10-12]
OMIM:109350	Gastroesophageal reflux		HP:0002020	OMIM:109350	TAS					P	HPO:probinson[2009-02-17]
OMIM:109350	Gastroesophageal reflux		HP:0100580	OMIM:109350	TAS					P	HPO:probinson[2015-02-01]
OMIM:109350	Gastroesophageal reflux		HP:0100751	OMIM:109350	TAS		10%			P	HPO:probinson[2009-02-17]
OMIM:109350	Gastroesophageal reflux		HP:0000006	OMIM:109350	TAS					I	HPO:probinson[2009-02-17]
OMIM:608567	Sick sinus syndrome 1		HP:0003577	PMID:14523039	PCS					C	HPO:skoehler[2013-01-22];HPO:probinson[2020-10-12]
OMIM:608567	Sick sinus syndrome 1		HP:0003621	PMID:14523039	PCS					C	HPO:probinson[2022-07-09]
OMIM:608567	Sick sinus syndrome 1		HP:0011704	PMID:14523039	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2020-10-12]
OMIM:608567	Sick sinus syndrome 1		HP:0011463	PMID:14523039	PCS					C	HPO:probinson[2022-07-09]
OMIM:608567	Sick sinus syndrome 1		HP:0005155	PMID:14523039	PCS					P	HPO:probinson[2012-04-10];HPO:probinson[2020-10-12]
OMIM:608567	Sick sinus syndrome 1		HP:0033122	PMID:14523039	PCS					P	HPO:probinson[2020-10-12]
OMIM:608567	Sick sinus syndrome 1		HP:0000007	PMID:14523039	PCS					I	HPO:probinson[2012-04-10];HPO:probinson[2020-10-12]
OMIM:608567	Sick sinus syndrome 1		HP:0001657	PMID:14523039	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2020-10-12]
OMIM:608567	Sick sinus syndrome 1		HP:0001678	PMID:14523039	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2020-10-12]
OMIM:608567	Sick sinus syndrome 1		HP:0001688	PMID:14523039	PCS					P	HPO:probinson[2012-04-10];HPO:probinson[2020-10-12]
OMIM:607654	Keratosis palmoplantaris striata III		HP:0001595	PMID:11982762	PCS		0/14			P	HPO:skoehler[2013-03-04];HPO:probinson[2020-07-23];HPO:probinson[2022-07-01]
OMIM:607654	Keratosis palmoplantaris striata III		HP:0001597	PMID:11982762	PCS		0/14			P	HPO:skoehler[2013-03-04];HPO:probinson[2020-07-23];HPO:probinson[2022-07-01]
OMIM:607654	Keratosis palmoplantaris striata III		HP:0011463	PMID:11982762	PCS		14/14			C	HPO:probinson[2022-07-01]
OMIM:607654	Keratosis palmoplantaris striata III		HP:0000982	PMID:11982762	PCS	HP:0011463	14/14			P	HPO:skoehler[2013-03-04];HPO:probinson[2020-07-23]
OMIM:607654	Keratosis palmoplantaris striata III		HP:0000006	PMID:11982762	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-23]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002487	PMID:27236917	PCS	HP:0011463				P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002069	PMID:27236917	PCS		1/8			P	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002059	PMID:27236917	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0006813	PMID:27236917	PCS		4/8			P	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001344	PMID:27236917	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002375	PMID:27236917	PCS		4/8			P	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001266	PMID:27236917	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002376	PMID:27236917	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001288	PMID:27236917	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001272	PMID:27236917	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002396	PMID:27236917	PCS		1/8			P	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001263	PMID:27236917	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002063	PMID:27236917	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001252	PMID:27236917	PCS		3/8			P	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0003593	PMID:27236917	PCS		2/8			C	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0002072	PMID:27236917	PCS		8/8			P	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0000639	PMID:27236917	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0011463	PMID:27236917	PCS		6/8			C	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0031165	PMID:27236917	PCS		2/8			P	HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0000007	PMID:27236917	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0200134	PMID:27236917	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001257	PMID:27236917	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:616981	Epileptic encephalopathy, early infantile, 37		HP:0001336	PMID:27236917	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-30]
OMIM:192600	Cardiomyopathy, familial hypertrophic 1		HP:0001682	OMIM:192600	IEA					P	HPO:iea[2009-02-17]
OMIM:192600	Cardiomyopathy, familial hypertrophic 1		HP:0001670	OMIM:192600	IEA					P	HPO:iea[2009-02-17]
OMIM:192600	Cardiomyopathy, familial hypertrophic 1		HP:0001635	OMIM:192600	IEA					P	HPO:iea[2009-02-17]
OMIM:192600	Cardiomyopathy, familial hypertrophic 1		HP:0011675	OMIM:192600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192600	Cardiomyopathy, familial hypertrophic 1		HP:0000006	PMID:1975517	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:192600	Cardiomyopathy, familial hypertrophic 1		HP:0001699	OMIM:192600	IEA					P	HPO:iea[2009-02-17]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0002015	PMID:25152456	PCS		2/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0000684	PMID:25152456	PCS		6/6			P	HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0004322	PMID:25152456	PCS		6/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0002043	PMID:25152456	PCS		2/6			P	HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0002099	PMID:25152456	PCS		3/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0003593	PMID:25152456	PCS		6/6			C	HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0025092	PMID:25152456	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0000407	PMID:25152456	PCS		3/6			P	HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0006297	PMID:25152456	PCS		6/6			P	HPO:skoehler[2015-08-16]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0000668	PMID:25152456	PCS		6/6			P	HPO:skoehler[2015-08-16]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0000007	PMID:25152456	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0008404	PMID:25152456	PCS		6/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0000982	PMID:25152456	PCS		6/6			P	HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0001798	PMID:25152456	PCS					P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-19]
OMIM:616029	Ectodermal dysplasia/short stature syndrome		HP:0000962	PMID:25152456	PCS				HP:0012825	P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-19]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000286	PMID:29276004	PCS		2/10			P	HPO:skoehler[2019-04-18]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002268	PMID:29276004	PCS		4/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002188	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002540	PMID:29276004	PCS		5/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000343	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000463	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001332	PMID:29276004	PCS		3/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002120	PMID:29276004	PCS		1/10			P	HPO:skoehler[2018-10-08]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001250	PMID:29276004	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001252	PMID:29276004	PCS		9/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0003593	PMID:29276004	PCS		7/10			C	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0010763	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0045075	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0011463	PMID:29276004	PCS		1/10			C	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000319	PMID:29276004	PCS		1/10			P	HPO:skoehler[2018-10-08]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000733	PMID:29276004	PCS		3/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000219	PMID:29276004	PCS		1/10			P	HPO:skoehler[2019-04-18]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002119	PMID:29276004	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000455	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001269	PMID:29276004	PCS		1/10			P	HPO:skoehler[2018-10-08]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000179	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001249	PMID:29276004	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0003623	PMID:29276004	PCS		2/10			C	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0003763	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002553	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000252	PMID:29276004	PCS		6/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001344	PMID:29276004	PCS		7/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002133	PMID:29276004	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000574	PMID:29276004	PCS		2/10			P	HPO:probinson[2023-05-07];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001321	PMID:29276004	PCS		1/10			P	HPO:skoehler[2018-10-08]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002376	PMID:29276004	PCS		5/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002079	PMID:29276004	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000490	PMID:29276004	PCS		2/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0001263	PMID:29276004	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000294	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002072	PMID:29276004	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0005280	PMID:29276004	PCS		2/10			P	HPO:skoehler[2019-04-18]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0002509	PMID:29276004	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000527	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0100716	PMID:29276004	PCS		2/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000268	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000400	PMID:29276004	PCS		2/10			P	HPO:skoehler[2019-04-18]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000006	PMID:29276004	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-07]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000347	PMID:29276004	PCS		1/10			P	HPO:skoehler[2018-10-08]
OMIM:618004	Epileptic encephalopathy, early infantile, 64		HP:0000687	PMID:29276004	PCS		1/10			P	HPO:probinson[2023-05-07]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0003774	OMIM:161950	TAS					P	HPO:skoehler[2013-07-01]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0000123	OMIM:161950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0000794	OMIM:161950	TAS					P	HPO:skoehler[2013-07-01]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0002829	OMIM:161950	TAS		HP:0040283			P	HPO:skoehler[2013-07-01]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0000979	OMIM:161950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0000790	OMIM:161950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0000822	OMIM:161950	TAS					P	HPO:skoehler[2013-07-01]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0000093	OMIM:161950	TAS					P	HPO:skoehler[2013-07-01]
OMIM:161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1		HP:0000006	OMIM:161950	TAS					I	HPO:skoehler[2013-05-29]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0000175	PMID:27838789	PCS		1/6			P	HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0000695	PMID:27838789	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0004552	PMID:27838789	PCS		1/6			P	HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0032541	PMID:27838789	PCS		2/6			P	HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0040162	PMID:27838789	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0008392	PMID:27838789	PCS		3/6			P	HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0040154	PMID:27838789	PCS		6/6			P	HPO:skoehler[2017-07-13]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0032152	PMID:27838789	PCS		5/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0033252	PMID:27838789	PCS		6/6			P	HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0011120	PMID:27838789	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0007387	PMID:27838789	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0000964	PMID:27838789	PCS		3/6			P	HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0000966	PMID:27838789	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0009886	PMID:27838789	PCS		1/6			P	HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0008404	PMID:27838789	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0000322	PMID:27838789	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0000006	PMID:27838789	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-16]
OMIM:617337	Ectodermal dysplasia 12, Hypohidrotic/hair/tooth/nail type		HP:0005338	PMID:27838789	PCS		6/6			P	HPO:probinson[2023-03-16]
OMIM:608217	Epilepsy, benign neonatal, 3		HP:0002069	OMIM:608217	IEA					P	HPO:iea[2009-02-17]
OMIM:608217	Epilepsy, benign neonatal, 3		HP:0003593	OMIM:608217	IEA					C	HPO:iea[2009-02-17]
OMIM:608217	Epilepsy, benign neonatal, 3		HP:0000006	OMIM:608217	IEA					I	HPO:iea[2009-02-17]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001298	PMID:17921179	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0003676	PMID:17921179	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000365	PMID:17921179	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001272	OMIM:271245	IEA					P	HPO:iea[2009-02-17]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002120	OMIM:271245	IEA					P	HPO:skoehler[2010-06-18]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0003693	PMID:17921179	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001252	PMID:17921179	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001251	PMID:17921179	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0003593	PMID:17921179	PCS		2/2			C	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0033685	PMID:17921179	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0003390	PMID:17921179	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0012847	PMID:17921179	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0031964	PMID:17921179	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000815	OMIM:271245	IEA					P	HPO:skoehler[2010-06-20]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000639	PMID:17921179	PCS		1/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000817	PMID:17921179	PCS		1/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001328	OMIM:271245	IEA					P	HPO:skoehler[2010-06-18]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0007366	OMIM:271245	TAS					P	HPO:skoehler[2017-07-13]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0008278	PMID:17921179	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001324	OMIM:271245	IEA					P	HPO:skoehler[2010-06-18]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001249	OMIM:271245	IEA					P	HPO:skoehler[2010-06-18]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002312	OMIM:271245	IEA					P	HPO:iea[2009-02-17]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002015	PMID:17921179	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0031956	PMID:17921179	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0003387	PMID:17921179	PCS		2/2			P	HPO:probinson[2023-01-26];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002133	PMID:17921179	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0003487	PMID:17921179	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002013	PMID:17921179	PCS		2/2			P	HPO:probinson[2023-01-26];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002076	OMIM:271245	IEA					P	HPO:skoehler[2010-06-20]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001284	PMID:17921179	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0001262	OMIM:271245	IEA					P	HPO:skoehler[2010-06-18]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000709	OMIM:271245	IEA					P	HPO:skoehler[2010-06-18]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000602	PMID:17921179	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000007	PMID:16135556	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0200134	OMIM:271245	TAS					P	HPO:skoehler[2013-06-11]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0000648	OMIM:271245	IEA					P	HPO:iea[2009-02-17]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002505	PMID:17921179	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0002305	PMID:17921179	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:271245	Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)		HP:0004305	PMID:17921179	PCS		2/2			P	HPO:probinson[2023-01-26];HPO:probinson[2023-01-26]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0000252	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0003236	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0003577	OMIM:613151	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0000486	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0001321	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0003560	OMIM:613151	TAS		20/20			P	HPO:skoehler[2015-01-19];HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0002350	OMIM:613151	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0001270	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0012110	OMIM:613151	TAS					P	HPO:skoehler[2014-09-21]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0000007	OMIM:613151	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0000648	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0002119	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0000545	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 3		HP:0001249	OMIM:613151	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605055	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology		HP:0001250	OMIM:605055	IEA					P	HPO:iea[2009-02-17]
OMIM:605055	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology		HP:0006790	OMIM:605055	IEA					P	HPO:iea[2009-02-17]
OMIM:605055	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology		HP:0002185	OMIM:605055	IEA					P	HPO:iea[2009-02-17]
OMIM:605055	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology		HP:0100256	OMIM:605055	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605055	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology		HP:0000006	OMIM:605055	IEA					I	HPO:iea[2009-02-17]
OMIM:605055	Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology		HP:0002511	OMIM:605055	IEA					P	HPO:iea[2009-02-17]
OMIM:612529	Amelogenesis imperfecta, hypomaturation type, iia2		HP:0000705	PMID:15744043	PCS		2/2			P	HPO:probinson[2013-03-12];HPO:probinson[2023-02-11]
OMIM:612529	Amelogenesis imperfecta, hypomaturation type, iia2		HP:0009102	PMID:15744043	PCS		1/2			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-11]
OMIM:612529	Amelogenesis imperfecta, hypomaturation type, iia2		HP:0006286	PMID:15744043	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:612529	Amelogenesis imperfecta, hypomaturation type, iia2		HP:0000007	PMID:15744043	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-02-11]
OMIM:612529	Amelogenesis imperfecta, hypomaturation type, iia2		HP:0033786	PMID:15744043	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0007417	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0002586	PMID:7795241;PMID:10498624	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002740	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0025044	PMID:7795241;PMID:10498624	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002840	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002741	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0033608	PMID:10498624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0025289	PMID:10498624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002240	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0003593	PMID:10498624	PCS		4/6			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0034752	PMID:10498624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0100523	PMID:10498624	PCS		1/6			P	HPO:probinson[2017-09-04]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0100721	PMID:10498624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0001508	PMID:7795241;PMID:10498624	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0002719	PMID:7795241;PMID:10498624	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0011463	PMID:7795241;PMID:10498624	PCS		3/7			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002716	PMID:10498624	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002955	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0006532	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0003206	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0009789	PMID:7795241;PMID:10498624	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0005406	PMID:7795241;PMID:10498624	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30];HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0001744	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002754	PMID:7795241;PMID:10498624	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30];HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0003203	PMID:7795241;PMID:10498624	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-06-30];HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0002037	PMID:10498624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0003621	OMIM:233710	IEA					C	HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0000010	PMID:7795241;PMID:10498624	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0005224	OMIM:233710	TAS					P	HPO:skoehler[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0009098	PMID:7795241;PMID:10498624	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0100658	OMIM:233710	TAS					P	HPO:probinson[2017-09-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002726	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0000007	PMID:10498624	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0000964	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002724	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Chronic granulomatous disease 2, autosomal recessive		HP:0002722	PMID:10498624	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002723	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002742	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002721	PMID:10498624	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2024-06-30]
OMIM:233710	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II		HP:0002842	OMIM:233710	IEA					P	HPO:iea[2009-02-17]
OMIM:608565	Deafness, autosomal recessive 35		HP:0031703	PMID:18179891	PCS		0/8			P	HPO:lccarmody[2018-06-29];HPO:probinson[2022-07-01]
OMIM:608565	Deafness, autosomal recessive 35		HP:0003577	PMID:18179891	PCS					C	HPO:probinson[2022-07-20]
OMIM:608565	Deafness, autosomal recessive 35		HP:0000407	PMID:18179891	PCS		8/8			P	HPO:probinson[2013-03-25];HPO:probinson[2022-07-01]
OMIM:608565	Deafness, autosomal recessive 35		HP:0000007	PMID:18179891	PCS					I	HPO:probinson[2013-03-25]
OMIM:608565	Deafness, autosomal recessive 35		HP:0000504	PMID:18179891	PCS		0/8			P	HPO:lccarmody[2018-06-29];HPO:probinson[2022-07-01]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0032615	PMID:31866046	PCS					P	HPO:probinson[2020-05-17]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0002521	PMID:31866046	PCS		1/3			P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0001250	PMID:31866046	PCS					P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0003593	PMID:31866046	PCS					C	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0011923	PMID:31866046	PCS					P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0012469	PMID:31866046	PCS		1/3			P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0000007	PMID:31866046	PCS					I	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0008872	PMID:31866046	PCS					P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0000648	PMID:31866046	PCS					P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0001511	PMID:31866046	PCS		1/3			P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0000543	PMID:31866046	PCS					P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0001942	PMID:31866046	PCS					P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0003128	PMID:31866046	PCS		3/3			P	HPO:probinson[2020-05-10]
OMIM:618776	Mitochondrial complex I deficiency, nuclear type 34		HP:0004887	PMID:31866046	PCS					P	HPO:probinson[2020-05-10]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0032417	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0002113	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0003774	PMID:23661805	PCS	HP:0003621	2/2			P	HP:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0002110	PMID:23661805	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0000083	PMID:23661805	PCS		1/2			P	HP:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0003593	PMID:23661805	PCS		2/2			C	HPO:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0012735	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0032622	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0001959	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0000007	PMID:23661805	PCS					I	HPO:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0001954	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0000103	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0002205	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19]
OMIM:619468	Nephronophthisis-like nephropathy 2		HP:0003259	PMID:23661805	PCS		2/2			P	HP:probinson[2021-10-19]
OMIM:142623	Hirschsprung disease, susceptibility to, 1		HP:0002013	OMIM:142623	IEA					P	HPO:iea[2009-02-17]
OMIM:142623	Hirschsprung disease, susceptibility to, 1		HP:0004387	OMIM:142623	IEA					P	HPO:iea[2009-02-17]
OMIM:142623	Hirschsprung disease, susceptibility to, 1		HP:0002251	OMIM:142623	IEA					P	HPO:iea[2009-02-17]
OMIM:142623	Hirschsprung disease, susceptibility to, 1		HP:0004362	OMIM:142623	TAS					P	HPO:iea[2015-05-23]
OMIM:142623	Hirschsprung disease, susceptibility to, 1		HP:0003270	OMIM:142623	IEA					P	HPO:iea[2009-02-17]
OMIM:142623	Hirschsprung disease, susceptibility to, 1		HP:0002019	OMIM:142623	IEA					P	HPO:iea[2009-02-17]
OMIM:142623	Hirschsprung disease, susceptibility to, 1		HP:0000006	OMIM:142623	IEA					I	HPO:iea[2009-02-17]
OMIM:221300	Deafness, conductive, with malformed external ear		HP:0004452	OMIM:221300	TAS					P	HPO:probinson[2009-02-17]
OMIM:221300	Deafness, conductive, with malformed external ear		HP:0000007	OMIM:221300	TAS					I	HPO:probinson[2009-02-17]
OMIM:221300	Deafness, conductive, with malformed external ear		HP:0000405	OMIM:221300	TAS					P	HPO:skoehler[2010-06-18]
OMIM:221300	Deafness, conductive, with malformed external ear		HP:0000135	OMIM:221300	TAS					P	HPO:probinson[2009-02-17]
OMIM:221300	Deafness, conductive, with malformed external ear		HP:0000377	OMIM:221300	TAS					P	HPO:probinson[2009-02-17]
OMIM:221300	Deafness, conductive, with malformed external ear		HP:0000369	OMIM:221300	TAS					P	HPO:probinson[2009-02-17]
OMIM:221300	Deafness, conductive, with malformed external ear		HP:0001249	OMIM:221300	TAS					P	HPO:probinson[2009-02-17]
OMIM:605041	Brooke-Spiegler syndrome		HP:0001056	OMIM:605041	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605041	Brooke-Spiegler syndrome		HP:0002664	OMIM:605041	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605041	Brooke-Spiegler syndrome		HP:0003581	OMIM:605041	IEA					C	HPO:skoehler[2010-06-19]
OMIM:605041	Brooke-Spiegler syndrome		HP:0000006	OMIM:605041	IEA					I	HPO:skoehler[2010-06-19]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0007737	OMIM:180210	IEA					P	HPO:iea[2009-02-17]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0000662	OMIM:180210	IEA					P	HPO:iea[2009-02-17]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0000618	OMIM:180210	TAS	HP:0003584				P	HPO:skoehler[2010-06-20]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0000580	OMIM:180210	TAS					P	HPO:probinson[2017-12-22]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0000488	OMIM:180210	IEA					P	HPO:skoehler[2015-12-30]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0007843	OMIM:180210	IEA					P	HPO:iea[2009-02-17]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0000006	OMIM:180210	IEA					I	HPO:iea[2009-02-17]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0000556	OMIM:180210	TAS					P	HPO:probinson[2015-07-20]
OMIM:180210	Retinopathy, pericentral pigmentary, dominant		HP:0001105	OMIM:180210	IEA					P	HPO:iea[2009-02-17]
OMIM:104110	Alopecia, familial focal		HP:0002232	OMIM:104110	TAS					P	HPO:probinson[2009-02-17]
OMIM:104110	Alopecia, familial focal		HP:0000006	OMIM:104110	TAS					I	HPO:iea[2009-02-17]
OMIM:268700	Saccharopinuria		HP:0001264	OMIM:268700	IEA					P	HPO:iea[2009-02-17]
OMIM:268700	Saccharopinuria		HP:0002353	OMIM:268700	IEA					P	HPO:iea[2009-02-17]
OMIM:268700	Saccharopinuria		HP:6000283	OMIM:268700	TAS		20/20			P	HPO:probinson[2021-10-03];HPO:probinson[2024-02-27]
OMIM:268700	Saccharopinuria		HP:0004322	OMIM:268700	IEA					P	HPO:iea[2009-02-17]
OMIM:268700	Saccharopinuria		HP:0003297	OMIM:268700	IEA					P	HPO:iea[2009-02-17]
OMIM:268700	Saccharopinuria		HP:0002927	OMIM:268700	IEA					P	HPO:iea[2009-02-17]
OMIM:268700	Saccharopinuria		HP:0032397	OMIM:268700	IEA					P	HPO:skoehler[2019-09-07]
OMIM:268700	Saccharopinuria		HP:0000007	OMIM:268700	IEA					I	HPO:iea[2009-02-17]
OMIM:268700	Saccharopinuria		HP:0034026	OMIM:268700	TAS					P	HPO:probinson[2021-10-03]
OMIM:268700	Saccharopinuria		HP:0001249	OMIM:268700	IEA					P	HPO:iea[2009-02-17]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0002069	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0002465	PMID:29603516	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0031703	OMIM:618010	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0006989	PMID:29573052	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0002123	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0001250	PMID:29573052	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0001290	PMID:29603516	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0000958	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0011463	PMID:29573052	PCS		2/2			C	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0000718	PMID:29573052	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0001328	PMID:29603516	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0000218	PMID:29603516	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0001864	PMID:29573052	PCS		1/2			P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0002754	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0004379	PMID:29573052	PCS		0/2			P	HPO:nvasilevsky[2019-03-27];HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0000252	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0002155	PMID:29573052	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0002373	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0025510	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0001263	OMIM:618010	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0100025	PMID:29573052	PCS		1/2			P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0000007	PMID:29573052	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0004209	PMID:29573052	PCS		1/2			P	HPO:nvasilevsky[2019-03-27]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0000389	PMID:29573052	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:618010	Glycosylphosphatidylinositol biosynthesis defect 17		HP:0001510	PMID:29573052	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:617323	Intellectual developmental disorder, autosomal recessive 59		HP:0000718	PMID:26416544	PCS		6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-16]
OMIM:617323	Intellectual developmental disorder, autosomal recessive 59		HP:0000007	PMID:26416544	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-16]
OMIM:617323	Intellectual developmental disorder, autosomal recessive 59		HP:0011999	PMID:26416544	PCS		6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-16]
OMIM:617323	Intellectual developmental disorder, autosomal recessive 59		HP:0001249	PMID:26416544	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-16]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0003203	PMID:10758162	PCS		1/1			P	HP:probinson[2019-03-02];HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0001058	PMID:10758162	PCS		1/1			P	HP:probinson[2019-03-02];HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0005224	PMID:10758162	PCS	HP:0003593	1/1			P	HP:probinson[2019-03-02];HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0005400	PMID:10758162	PCS		1/1			P	HP:probinson[2019-03-02];HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0012618	PMID:10758162	PCS		1/1			P	HP:probinson[2019-03-02];HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0032434	PMID:10758162	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0032435	PMID:21167572	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0031545	PMID:21167572	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0011897	PMID:10758162	PCS		1/1			P	HP:probinson[2019-03-02];HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0011897	PMID:21167572	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0040238	PMID:21167572;PMID:10758162	PCS		2/2			P	HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0001972	PMID:21167572	PCS	HP:0003593	1/1			P	HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0000006	PMID:10758162	PCS					I	HPO:probinson[2020-12-04]
OMIM:608203	Immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis		HP:0001974	PMID:21167572	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-04]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0002224	PMID:18982349	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0002583	PMID:22444670;PMID:18982349	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0030056	PMID:22444670	PCS					P	HPO:skoehler[2015-01-20];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0003593	PMID:22444670	PCS					C	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0002240	PMID:18982349	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0001394	PMID:22444670	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0025085	PMID:18982349	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0008070	PMID:22444670	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0001508	PMID:22444670	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0011220	PMID:22444670	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0011461	PMID:18982349	PCS		1/1			C	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0000316	PMID:22444670	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0200123	PMID:18982349	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0009886	PMID:22444670;PMID:18982349	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0001622	PMID:22444670;PMID:18982349	PCS		3/6			P	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0003623	PMID:22444670	PCS					C	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0002014	PMID:22444670	PCS		6/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0000431	PMID:18982349	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0002299	PMID:22444670	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0005280	PMID:22444670	PCS					P	HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0040303	PMID:18982349	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0001518	PMID:22444670;PMID:18982349	PCS		11/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0011473	PMID:22444670	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0000007	PMID:22444670	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0001511	PMID:22444670	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0002721	PMID:22444670	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-12]
OMIM:614602	Trichohepatoenteric syndrome 2		HP:0002028	PMID:18982349	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:609135	Aplastic anemia		HP:0001915	PMID:12090986	PCS		HP:0040280			P	HPO:skoehler[2015-08-23];HP:probinson[2018-07-14]
OMIM:609135	Aplastic anemia		HP:0005528	PMID:12090986	PCS					P	HPO:skoehler[2015-08-23]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0008947	PMID:32936766	PCS	HP:0003593	2/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000044	PMID:26120850;PMID:32936766	PCS		2/4			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000054	PMID:32936766	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000771	PMID:32936766	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000293	PMID:32936766	PCS		3/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0030341	PMID:32936766	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0040171	PMID:32936766	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0001270	PMID:32936766	PCS		3/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0011787	PMID:32936766	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0031098	PMID:32936766	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0033078	PMID:32936766	PCS		3/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000007	PMID:32936766	PCS					I	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000823	PMID:32936766	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000400	PMID:32936766	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000311	PMID:32936766	PCS		3/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0001631	PMID:32936766	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0005978	PMID:26120850	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0001513	PMID:26120850;PMID:32936766	PCS		3/4			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000347	PMID:32936766	PCS		3/3			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000028	PMID:32936766	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0001249	PMID:26120850;PMID:32936766	PCS		4/4			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000842	PMID:32936766	PCS		1/2			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0000786	PMID:26120850;PMID:32936766	PCS		2/2			P	HPO:probinson[2021-07-04]
OMIM:619326	Intellectual developmental disorder and hypogonadotropic hypogonadism		HP:0033082	PMID:32936766	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:121390	Cornea guttata with anterior polar cataracts		HP:0001134	OMIM:121390	IEA					P	HPO:iea[2009-02-17]
OMIM:121390	Cornea guttata with anterior polar cataracts		HP:0000505	OMIM:121390	IEA					P	HPO:iea[2009-02-17]
OMIM:121390	Cornea guttata with anterior polar cataracts		HP:0000006	OMIM:121390	IEA					I	HPO:iea[2009-02-17]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0002840	PMID:30723080	PCS	HP:0003593	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0002783	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0031545	PMID:30723080	PCS	HP:0003577	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0100806	PMID:30723080	PCS	HP:0003593	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0001888	PMID:30723080	PCS		3/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0006532	PMID:30723080	PCS	HP:0003593	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0006510	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0410305	PMID:30723080	PCS		1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0040238	PMID:30723080;PMID:30654050	PCS		12/12			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0004315	PMID:31071452;PMID:30654050	PCS		3/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0005403	PMID:30654050	PCS		3/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0001882	PMID:31071452;PMID:30654050	PCS		3/4			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0002110	PMID:30723080	PCS	HP:0011462	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0012312	PMID:30654050	PCS		2/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0011108	PMID:30723080	PCS	HP:0003593				P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0010976	PMID:30654050	PCS		3/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0032170	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0031382	PMID:30654050	PCS		2/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0100658	PMID:30723080	PCS	HP:0003593	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0000403	PMID:30723080	PCS	HP:0003621	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0000403	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0008940	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0002205	PMID:30654050	IEA		3/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0001433	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0002206	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0000006	PMID:30723080	PCS					I	HPO:probinson[2020-09-07];HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0001876	PMID:30723080	PCS	HP:0003593	1/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0001875	PMID:30654050	PCS		3/3			P	HPO:probinson[2020-09-07]
OMIM:618986	Immunodeficiency 73B with defective neutrophil chemotaxis and lymphopenia		HP:0004469	PMID:31071452	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:614164	Glutathione peroxidase deficiency		HP:0020082	OMIM:614164	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614164	Glutathione peroxidase deficiency		HP:0004863	OMIM:614164	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614164	Glutathione peroxidase deficiency		HP:0003265	OMIM:614164	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614164	Glutathione peroxidase deficiency		HP:0000007	OMIM:614164	TAS					I	HPO:skoehler[2012-10-17]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001298	PMID:17187620;PMID:15499950	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003477	PMID:31844624;PMID:35112411	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000365	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003596	PMID:34746378	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000486	PMID:23838601;PMID:29351582;PMID:31844624	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001695	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003198	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003593	PMID:10805329;PMID:23838601;PMID:10545952;PMID:29351582;PMID:17187620;PMID:10749987;PMID:15499950;PMID:23364397	PCS		16/22			C	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0012747	PMID:20159436	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000639	PMID:10805329;PMID:10545952	PCS		4/6			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0012195	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0200147	OMIM:604377	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001605	PMID:18924171	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007204	PMID:35112411	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001324	PMID:16765077;PMID:18924171;PMID:23364397	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007327	PMID:29351582	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003623	PMID:23407777;PMID:10545952	PCS		3/4			C	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000252	PMID:23838601;PMID:15499950	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0031318	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002151	PMID:16765077;PMID:20159436;PMID:19353847;PMID:10545952;PMID:14994243;PMID:31844624;PMID:10749987;PMID:35112411	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000007	PMID:10545952	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002789	PMID:17187620	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000369	PMID:19353847	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001337	PMID:31844624;PMID:35112411	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001336	PMID:23838601	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001276	PMID:15499950	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003577	PMID:16765077;PMID:20159436;PMID:15210538;PMID:19353847;PMID:18924171;PMID:14994243;PMID:10749987;PMID:15499950	PCS		9/15			C	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001310	PMID:31844624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0010307	PMID:14994243	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001272	PMID:10545952;PMID:10749987;PMID:31844624	PCS		3/5			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002120	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003693	PMID:31844624	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002363	PMID:18924171	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001273	PMID:18924171	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002240	PMID:20159436;PMID:23838601;PMID:10545952	PCS		4/5			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0032653	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0012444	PMID:23838601;PMID:10545952;PMID:15499950	PCS		8/10			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007141	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002518	PMID:18924171	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002878	PMID:16765077;PMID:10749987;PMID:15499950;PMID:35112411	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002119	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000218	PMID:20159436;PMID:10545952	PCS		2/4			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002359	PMID:29351582;PMID:31844624;PMID:35112411	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007941	OMIM:604377	IEA					P	HPO:iea[2009-02-17]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003688	PMID:23407777;PMID:17187620;PMID:10749987;PMID:15499950	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001942	PMID:10805329;PMID:10749987	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001667	PMID:14994243;PMID:35112411	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0006855	PMID:31844624	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000577	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003621	PMID:29351582;PMID:35112411	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000750	PMID:35112411	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002376	PMID:23838601	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002098	PMID:10805329;PMID:15210538;PMID:19353847;PMID:10545952	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002495	PMID:29351582;PMID:35112411	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001284	PMID:34746378;PMID:18924171;PMID:14994243	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002094	PMID:17187620	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002490	PMID:10545952;PMID:31844624	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0012047	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000508	PMID:16765077;PMID:23838601;PMID:29351582	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0009830	PMID:16765077;PMID:10805329	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002529	PMID:10545952	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0008347	OMIM:604377	TAS					P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000505	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000741	PMID:20159436	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002403	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003458	PMID:10805329	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001254	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002188	PMID:23838601	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001250	PMID:18924171;PMID:10749987;PMID:35112411	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002066	PMID:31844624	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001252	PMID:20159436;PMID:23407777;PMID:10805329;PMID:19353847;PMID:15210538;PMID:23838601;PMID:10545952;PMID:18924171;PMID:14994243;PMID:17187620;PMID:10749987;PMID:15499950	PCS		20/23			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001251	PMID:34746378;PMID:23838601	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0033526	PMID:35112411	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0011463	PMID:31844624;PMID:35112411	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007089	PMID:29351582	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007002	PMID:23407777;PMID:29351582	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001800	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001522	PMID:10545952	PCS		3/3			C	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001763	PMID:29351582	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000952	PMID:20159436	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001265	PMID:10805329;PMID:31844624;PMID:15499950;PMID:35112411	PCS		9/10			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0005348	PMID:23407777;PMID:10545952;PMID:18924171;PMID:10749987;PMID:15499950	PCS		7/9			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0030148	PMID:15210538	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001662	PMID:18924171;PMID:35112411	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002354	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0011968	PMID:16765077;PMID:20159436;PMID:10545952	PCS		3/5			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001260	PMID:29351582	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001263	PMID:23838601;PMID:10545952;PMID:35112411;PMID:23364397	PCS		13/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0032046	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002194	PMID:29351582;PMID:31844624;PMID:35112411	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0009130	PMID:35112411	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002509	PMID:23364397	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0006543	PMID:10805329	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002505	PMID:29351582	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002747	PMID:23407777;PMID:15210538	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003438	PMID:19353847;PMID:29351582;PMID:31844624;PMID:35112411	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002500	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003557	PMID:10545952	PCS		1/1			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0004887	PMID:16765077;PMID:20159436;PMID:10805329;PMID:23407777;PMID:15210538;PMID:18924171;PMID:14994243;PMID:17187620;PMID:15499950;PMID:35112411	PCS		16/17			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002047	PMID:23364397	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002683	PMID:20159436	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003376	PMID:29351582	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0030319	PMID:29351582;PMID:35112411	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0040081	PMID:34746378;PMID:23838601;PMID:29351582	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007183	PMID:20159436	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001508	PMID:20159436;PMID:23838601	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0007340	PMID:29351582;PMID:35112411	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003648	PMID:23838601	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003128	PMID:16765077;PMID:20159436;PMID:23407777;PMID:15210538;PMID:10545952;PMID:14994243;PMID:35112411	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0006999	PMID:10545952	PCS		1/1			P	HPO:probinson[2013-11-24];HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002059	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000431	PMID:20159436	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001640	PMID:23407777	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0003542	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001761	PMID:29351582	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002451	PMID:10805329;PMID:10545952	PCS		4/6			P	HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0200049	PMID:23407777	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0002171	PMID:10545952	PCS		3/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0012514	PMID:34746378	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0033399	PMID:23364397	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0005280	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001639	PMID:16765077;PMID:20159436;PMID:10805329;PMID:15210538;PMID:19353847;PMID:10545952;PMID:18924171;PMID:14994243;PMID:17187620;PMID:10749987;PMID:15499950	PCS		18/22			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000308	PMID:20159436	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001999	PMID:10805329	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001635	PMID:10805329;PMID:14994243;PMID:35112411	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0000268	PMID:10545952	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001511	PMID:16765077;PMID:19353847	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0008944	PMID:29351582;PMID:35112411	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:604377	Mitochondrial complex IV deficiency, nuclear type 2		HP:0001875	PMID:17187620	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:614170	Brittle cornea syndrome 2		HP:0000365	PMID:21664999	PCS		8/8			P	HPO:probinson[2014-05-24];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0000563	PMID:21664999	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0001288	PMID:21664999	PCS		2/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0000023	PMID:21664999	PCS		1/8			P	HPO:probinson[2014-05-24];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0000485	PMID:21664999	PCS		0/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0001382	PMID:21664999	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0000592	PMID:21664999	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0100583	PMID:21664999	PCS		4/8			P	HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0100689	PMID:21664999	PCS		2/2			P	HPO:probinson[2014-05-24];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0001119	PMID:21664999	PCS		4/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0001537	PMID:21664999	PCS		1/8			P	HPO:probinson[2014-05-24];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0000007	PMID:21664999	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0002757	PMID:21664999	PCS		2/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0000978	PMID:21664999	PCS		4/8			P	HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0007720	OMIM:614170	TAS		HP:0040283			P	HPO:skoehler[2013-10-22]
OMIM:614170	Brittle cornea syndrome 2		HP:0000647	PMID:21664999	PCS		2/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0000545	PMID:21664999	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-16]
OMIM:614170	Brittle cornea syndrome 2		HP:0003326	PMID:21664999	PCS		3/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-16]
OMIM:600105	Retinitis pigmentosa 12		HP:0000550	PMID:19140180	PCS		3/3			P	HPO:probinson[2022-06-22];HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0007737	PMID:19140180	PCS		5/6			P	HPO:probinson[2022-06-22];HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0000662	OMIM:600105	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600105	Retinitis pigmentosa 12		HP:0000639	PMID:19140180	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0011463	PMID:19140180	PCS					C	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0008499	PMID:19140180	PCS		4/7			P	HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0000007	OMIM:600105	IEA					I	HPO:iea[2009-02-17]
OMIM:600105	Retinitis pigmentosa 12		HP:0007663	PMID:19140180	PCS		7/7			P	HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0000510	PMID:19140180	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0000543	PMID:19140180	PCS		5/6			P	HPO:probinson[2022-06-22];HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0007843	PMID:19140180	PCS		4/4			P	HPO:probinson[2022-06-22]
OMIM:600105	Retinitis pigmentosa 12		HP:0000577	PMID:19140180	PCS		2/7			P	HPO:probinson[2022-06-22]
OMIM:193250	Volvulus of midgut		HP:0005234	OMIM:193250	IEA					P	HPO:iea[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0000506	OMIM:193250	IEA					P	HPO:iea[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0002580	OMIM:193250	TAS					P	HPO:probinson[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0000348	OMIM:193250	IEA					P	HPO:iea[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0000637	OMIM:193250	IEA					P	HPO:iea[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0000119	OMIM:193250	IEA					P	HPO:iea[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0003270	OMIM:193250	TAS					P	HPO:probinson[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0002007	OMIM:193250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193250	Volvulus of midgut		HP:0002019	OMIM:193250	IEA					P	HPO:iea[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0000006	OMIM:193250	IEA					I	HPO:iea[2009-02-17]
OMIM:193250	Volvulus of midgut		HP:0002566	OMIM:193250	IEA					P	HPO:iea[2009-02-17]
OMIM:137280	Gastritis, familial giant hypertrophic		HP:0005246	OMIM:137280	IEA					P	HPO:iea[2009-02-17]
OMIM:137280	Gastritis, familial giant hypertrophic		HP:0003075	OMIM:137280	IEA					P	HPO:iea[2009-02-17]
OMIM:137280	Gastritis, familial giant hypertrophic		HP:0000007	OMIM:137280	TAS					I	HPO:skoehler[2017-07-13]
OMIM:137280	Gastritis, familial giant hypertrophic		HP:0002617	OMIM:137280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0001022	PMID:14961451	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-05-23]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0005599	PMID:11574907	PCS					P	HPO:probinson[2013-02-25]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0000639	PMID:14961451	PCS		9/18			P	HPO:probinson[2013-02-25];HPO:probinson[2020-05-23]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0000635	PMID:14961451	PCS					P	HPO:probinson[2013-02-25]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0000007	PMID:11574907	PCS					I	HPO:probinson[2013-01-09]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0007894	PMID:11574907	PCS					P	HPO:probinson[2013-02-25]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0000505	PMID:14722913	PCS					P	HPO:probinson[2013-02-25];HPO:probinson[2020-05-23]
OMIM:606574	Albinism, oculocutaneous, type IV		HP:0001104	PMID:14722913	PCS					P	HPO:probinson[2013-02-25];HPO:probinson[2020-05-23]
OMIM:609647	Deafness, neurosensory, autosomal recessive 46		HP:0000007	PMID:15637723	PCS					I	HPO:probinson[2009-02-17];HPO:lccarmody[2018-10-02]
OMIM:609647	Deafness, neurosensory, autosomal recessive 46		HP:0011476	PMID:15637723	PCS	HP:0003593	9/9			P	HPO:skoehler[2012-07-18];HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-14]
OMIM:609647	Deafness, neurosensory, autosomal recessive 46		HP:0008555	PMID:15637723	PCS		0/9			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-14]
OMIM:609647	Deafness, neurosensory, autosomal recessive 46		HP:0001249	PMID:15637723	PCS		0/9			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-14]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0003687	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0031936	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0003198	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0025335	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0030234	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0002121	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0000007	PMID:31469168	PCS					I	HPO:probinson[2020-09-07];HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0002518	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0001270	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:618992	Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15		HP:0003557	PMID:31469168	PCS		1/1			P	HPO:probinson[2020-09-07]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0000385	PMID:24781087	PCS		1/3			P	HPO:skoehler[2014-10-10];HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0002553	PMID:24781087	PCS		2/3			P	HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0000463	PMID:24781087	PCS		2/3			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0002561	PMID:24781087	PCS	HP:0003577	2/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0100853	PMID:24781087	PCS		1/3			P	HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0000319	PMID:24781087	PCS		2/3			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0032077	PMID:24781087	PCS		1/2	MALE		P	HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0000007	PMID:24781087	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0007598	PMID:24781087	PCS		1/3			P	HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0000455	PMID:24781087	PCS		2/3			P	HPO:skoehler[2014-09-21];HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0002557	PMID:24781087	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0000028	PMID:24781087	PCS		1/2	MALE		P	HPO:probinson[2021-10-21]
OMIM:616001	Breasts and/or nipples, aplasia or hypoplasia of, 2		HP:0000687	PMID:24781087	PCS		1/3			P	HPO:probinson[2021-10-21]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000044	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001770	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002023	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001171	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000081	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0045075	OMIM:129900	TAS					P	HPO:probinson[2022-05-08]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000316	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000437	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000635	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001803	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000677	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001249	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002215	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000054	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000252	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000175	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000453	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000691	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001739	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000968	OMIM:129900	IEA					P	HPO:skoehler[2015-01-14]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000327	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002507	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000405	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0007513	OMIM:129900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000963	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002225	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000204	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000006	OMIM:129900	IEA					I	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000962	OMIM:129900	PCS				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000126	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000143	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000145	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000023	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002164	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002286	OMIM:129900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000581	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001592	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0008070	OMIM:129900	PCS		20/20			P	HPO:iea[2009-02-17];HPO:iea[2012-03-01]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0008551	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000217	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000613	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000653	OMIM:129900	PCS					P	HPO:iea[2012-03-01]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002557	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000455	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000015	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000498	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000110	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000198	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000076	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000670	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000072	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001161	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000272	OMIM:129900	IEA				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000070	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000506	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0001839	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002209	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000824	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0002205	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000620	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000028	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000104	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:129900	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome1		HP:0000863	OMIM:129900	IEA					P	HPO:iea[2009-02-17]
OMIM:212090	Cardiac septal defects with coarctation of the aorta		HP:0001684	OMIM:212090	TAS					P	HPO:skoehler[2010-06-20]
OMIM:212090	Cardiac septal defects with coarctation of the aorta		HP:0011682	OMIM:212090	TAS					P	HPO:skoehler[2012-07-28]
OMIM:212090	Cardiac septal defects with coarctation of the aorta		HP:0001680	OMIM:212090	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212090	Cardiac septal defects with coarctation of the aorta		HP:0000007	OMIM:212090	TAS					I	HPO:skoehler[2009-02-17]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002783	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0011935	PMID:825775	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001252	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001890	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0003593	PMID:402573	PCS		1/1			C	HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001251	PMID:11453975	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001290	OMIM:613179	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0005372	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001270	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0005390	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0012410	PMID:11453975	PCS		1/1			P	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001904	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001508	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002718	OMIM:613179	TAS					P	HPO:probinson[2012-04-26]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001888	PMID:11453975	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001744	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001249	OMIM:613179	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002732	OMIM:613179	TAS					P	HPO:skoehler[2010-06-20]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001264	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0000010	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002273	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002194	PMID:11453975	PCS		1/1			P	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002090	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0011840	OMIM:613179	TAS				HP:0012828	P	HPO:probinson[2017-09-11]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0033339	PMID:402573	PCS					P	HPO:probinson[2020-12-07]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0040422	PMID:825775	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0000708	OMIM:613179	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0040424	PMID:825775	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0031381	PMID:11453975	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0033340	PMID:402573	PCS					P	HPO:probinson[2020-12-07]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0000007	PMID:11453975	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0004429	PMID:11453975	PCS					P	HPO:probinson[2012-04-26];HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0000246	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002788	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001973	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0000388	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0003537	PMID:402573	PCS	HP:0003593	1/1			P	HPO:skoehler[2014-05-24];HPO:probinson[2020-09-13]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0003537	PMID:825775	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0005318	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0001337	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613179	Immunodeficiency due to purine nucleoside phosphorylase deficiency		HP:0002665	OMIM:613179	IEA					P	HPO:skoehler[2010-06-19]
OMIM:614616	Diarrhea 6		HP:0100502	PMID:22436048	PCS		6/32			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:614616	Diarrhea 6		HP:0100280	PMID:22436048	PCS		4/32			P	HPO:probinson[2022-11-06]
OMIM:614616	Diarrhea 6		HP:0003593	PMID:22436048	PCS					C	HPO:probinson[2022-11-06]
OMIM:614616	Diarrhea 6		HP:6000319	PMID:22436048	PCS		27/28			P	HPO:probinson[2024-02-27]
OMIM:614616	Diarrhea 6		HP:0000006	PMID:22436048	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614616	Diarrhea 6		HP:0002027	PMID:22436048	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:614616	Diarrhea 6		HP:0002028	PMID:22436048	PCS		32/32			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0003577	PMID:23974871	PCS		3/3			C	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0003212	PMID:23974871	PCS		3/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0002024	PMID:23974871	PCS		3/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0003073	PMID:23974871	PCS		3/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0410151	PMID:23974871	PCS		1/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0040162	PMID:23974871	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0100792	PMID:23974871	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0008070	PMID:23974871	PCS		1/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0001508	PMID:23974871	PCS		3/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0003228	PMID:23974871	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0001642	PMID:23974871	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0003765	PMID:23974871	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0000252	PMID:23974871	PCS		2/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0025114	PMID:23974871	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0001263	PMID:23974871	PCS		3/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0001581	PMID:23974871	PCS		2/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0034323	PMID:23974871	PCS		1/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0011625	PMID:23974871	PCS		1/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0008064	PMID:23974871	PCS	HP:0003577	3/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0500093	PMID:23974871	PCS		3/3			P	HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0000007	PMID:23974871	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0001019	PMID:23974871	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0002205	PMID:23974871	PCS		3/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0001510	PMID:23974871	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-19]
OMIM:615508	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige		HP:0000982	PMID:23974871	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-19]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0007902	PMID:14507768	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0030666	PMID:15488808	PCS		0/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0000541	PMID:14507768;PMID:12172548	PCS		6/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0003581	PMID:15488808	PCS		1/2			C	HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0003593	PMID:15488808	PCS		1/2			C	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0001493	PMID:14507768	PCS		4/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0100832	PMID:14507768	PCS		8/12			P	HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0011530	PMID:14507768;PMID:15488808	PCS		4/14			P	HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0000618	OMIM:133780	IEA					P	HPO:iea[2009-02-17]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0007663	PMID:14507768;PMID:15488808	PCS		12/14			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0007685	PMID:14507768;PMID:15488808	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0002757	OMIM:133780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0025007	PMID:14507768	PCS		4/12			P	HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0001489	OMIM:133780	IEA					P	HPO:iea[2009-02-17]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0030490	PMID:15488808	PCS		1/2			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0000565	PMID:15488808	PCS		1/2			P	HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0001147	PMID:14507768	PCS		3/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0000523	PMID:14507768	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0003677	PMID:14507768	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:133780	Exudative vitreoretinopathy 1		HP:0000006	PMID:12172548	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:164800	Nail disorder, nonsyndromic congenital, 5		HP:0008400	OMIM:164800	IEA					P	HPO:iea[2009-02-17]
OMIM:164800	Nail disorder, nonsyndromic congenital, 5		HP:0007410	OMIM:164800	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:164800	Nail disorder, nonsyndromic congenital, 5		HP:0000006	OMIM:164800	IEA					I	HPO:iea[2009-02-17]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0001250	OMIM:613192	TAS		HP:0040283			P	HPO:skoehler[2013-06-03]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0003593	PMID:20004764	PCS		3/3			C	HPO:skoehler[2013-06-03];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000319	PMID:20004764	PCS		2/3			P	HPO:skoehler[2013-08-10];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0007068	PMID:20004763	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000316	PMID:20004764	PCS		1/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0002714	OMIM:613192	TAS		HP:0040283			P	HPO:probinson[2013-06-02]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000752	PMID:20004764	PCS		2/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0001249	PMID:20004764	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0003763	PMID:20004763	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000431	OMIM:613192	TAS		HP:0040283			P	HPO:probinson[2013-06-02]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000750	PMID:20004763;PMID:20004764	PCS		4/6			P	HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0002079	PMID:20004763	PCS		2/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0031936	OMIM:613192	IEA					P	HPO:skoehler[2019-02-22]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0001263	PMID:20004764	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000470	PMID:20004764	PCS		2/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0005484	OMIM:613192	TAS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0040196	PMID:20004764	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0100023	PMID:20004763	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000601	PMID:20004764	PCS		1/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000007	PMID:20004763	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0001956	PMID:20004764	PCS		3/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000664	OMIM:613192	TAS		HP:0040283			P	HPO:probinson[2013-06-02]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000322	PMID:20004764	PCS		2/3			P	HPO:skoehler[2013-08-10];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0001238	PMID:20004764	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0000204	PMID:20004764	PCS		1/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-06-15]
OMIM:613192	Intellectual developmental disorder, autosomal recessive 13		HP:0002500	PMID:20004764	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0003015	PMID:37582359	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000341	PMID:37582359	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0003577	PMID:37582359	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0002684	PMID:37582359	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000463	PMID:37582359	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0003593	PMID:37582359	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0004482	PMID:37582359	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0100670	PMID:37582359	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0001270	PMID:37582359	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0012444	PMID:37582359	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0001629	PMID:37582359	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000935	PMID:37582359	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0011001	PMID:37582359	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0011463	PMID:37582359	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0100702	PMID:37582359	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000316	PMID:37582359	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0004618	PMID:37582359	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0001643	PMID:37582359	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0001302	PMID:37582359	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000256	PMID:37582359	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0003623	PMID:37582359	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0001385	PMID:37582359	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0002079	PMID:37582359	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000452	PMID:37582359	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0001263	PMID:37582359	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:5200001	PMID:37582359	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0005280	PMID:37582359	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0012731	PMID:37582359	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0012541	PMID:37582359	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000007	PMID:37582359	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0002007	PMID:37582359	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0001631	PMID:37582359	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620558	Craniometadiaphyseal osteosclerosis with hip dysplasia		HP:0000520	PMID:37582359	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:600850	Schizophrenia 4		HP:0100753	PMID:12217952	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-07-20]
OMIM:600850	Schizophrenia 4		HP:0008358	PMID:12217952	PCS		4/4			P	HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:600850	Schizophrenia 4		HP:0000006	PMID:12217952	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:311200	Orofaciodigital syndrome I		HP:0000286	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0001056	PMID:11179005	PCS	HP:0003593	4/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000365	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0004322	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000161	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0001250	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0010442	PMID:11179005	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0010297	PMID:11179005	PCS		1/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0010296	PMID:11179005	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000316	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000238	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0009466	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0002617	OMIM:311200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:311200	Orofaciodigital syndrome I		HP:0001407	PMID:11179005	PCS		1/7			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0001885	PMID:11179005	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0002536	OMIM:311200	TAS					P	HPO:skoehler[2012-11-21]
OMIM:311200	Orofaciodigital syndrome I		HP:0000113	PMID:11179005	PCS	HP:0003581	3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0001249	PMID:11179005	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000175	PMID:11179005	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000494	PMID:11179005	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000252	OMIM:311200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0002475	OMIM:311200	TAS		HP:0040283			P	HPO:skoehler[2014-04-04]
OMIM:311200	Orofaciodigital syndrome I		HP:0002350	PMID:11179005	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000093	OMIM:311200	TAS					P	HPO:skoehler[2012-11-21]
OMIM:311200	Orofaciodigital syndrome I		HP:0011802	PMID:11179005	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0001737	PMID:11179005	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000369	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000204	PMID:11179005	PCS		3/7			P	HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0006349	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000324	PMID:11179005	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0003577	PMID:11179005	PCS		7/7			C	HPO:probinson[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0002444	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0001596	PMID:11179005	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0001156	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0001274	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0001395	OMIM:311200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0002282	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000180	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0008070	OMIM:311200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:311200	Orofaciodigital syndrome I		HP:0011359	PMID:11179005	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0009085	OMIM:311200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0100702	OMIM:311200	TAS					P	HPO:skoehler[2012-11-21]
OMIM:311200	Orofaciodigital syndrome I		HP:0006297	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0001627	OMIM:311200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0030084	PMID:11179005	PCS		2/7			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000218	PMID:11179005	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0001423	PMID:11179005	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000138	OMIM:311200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000670	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0002059	PMID:11179005	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000431	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000199	OMIM:311200	TAS					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000430	PMID:11179005;OMIM:311200	PCS		11/16			P	HPO:probinson[2022-03-27];HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0002132	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0011069	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000308	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000506	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0000822	OMIM:311200	TAS					P	HPO:skoehler[2012-11-21]
OMIM:311200	Orofaciodigital syndrome I		HP:0002007	OMIM:311200	IEA					P	HPO:iea[2009-02-17]
OMIM:311200	Orofaciodigital syndrome I		HP:0001159	PMID:11179005	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:311200	Orofaciodigital syndrome I		HP:0000268	PMID:11179005	PCS		1/6			P	HPO:probinson[2022-03-27]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0010628	OMIM:601596	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003431	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0000365	PMID:14574644	PCS		2/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0004466	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003693	PMID:14574644	PCS		15/18			P	HPO:probinson[2013-03-14];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0002460	PMID:14574644	PCS		18/18			P	HPO:probinson[2013-03-14];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003593	PMID:14574644	PCS		7/17			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0001270	OMIM:601596	IEA					P	HPO:iea[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0001291	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0012473	OMIM:601596	TAS					P	HPO:skoehler[2013-11-28]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0000639	PMID:14574644	PCS		1/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0011463	PMID:14574644	PCS		2/17			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0040078	OMIM:601596	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0002936	PMID:14574644	PCS		18/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0001308	OMIM:601596	TAS					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003701	PMID:14574644	PCS		9/18			P	HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0007107	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0001765	PMID:14574644	PCS		9/18			P	HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003400	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003621	PMID:14574644	PCS		8/17			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003387	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0002650	PMID:14574644	PCS		11/18			P	HPO:probinson[2012-03-13];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0001762	PMID:14574644	PCS		5/18			P	HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0001288	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0001761	PMID:14574644	PCS		9/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0003484	OMIM:601596	TAS					P	HPO:probinson[2012-03-13]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0034347	PMID:14574644	PCS		1/18			P	HPO:probinson[2022-09-05]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0007695	OMIM:601596	IEA					P	HPO:probinson[2009-02-17]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0000007	PMID:14574644	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:601596	Charcot-Marie-Tooth disease, type 4C		HP:0000764	OMIM:601596	TAS					P	HPO:probinson[2009-02-17]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000275	PMID:29374277	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000582	PMID:29374277	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000276	PMID:29374277	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0001250	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0001263	PMID:29374277	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0011822	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0011245	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000319	PMID:29374277	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000718	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000729	PMID:29374277	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000739	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000337	PMID:29374277	PCS		2/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000219	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0001417	PMID:29374277	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000752	PMID:29374277	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000400	PMID:29374277	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0007018	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0009899	PMID:29374277	PCS		2/6			P	HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0001249	PMID:29374277	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0000303	PMID:29374277	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:301013	Intellectual developmental disorder, X-linked 107		HP:0001513	PMID:29374277	PCS		1/6			P	HPO:probinson[2021-09-27]
OMIM:607859	Angioma, tufted		HP:0001000	OMIM:607859	IEA					P	HPO:skoehler[2009-02-17]
OMIM:607859	Angioma, tufted		HP:0011276	OMIM:607859	TAS					P	HPO:skoehler[2013-06-05]
OMIM:607859	Angioma, tufted		HP:0003829	OMIM:607859	TAS					I	HPO:skoehler[2012-10-17]
OMIM:607859	Angioma, tufted		HP:0012329	OMIM:607859	TAS					P	HPO:probinson[2013-08-13]
OMIM:607859	Angioma, tufted		HP:0000006	OMIM:607859	TAS					I	HPO:probinson[2012-07-21]
OMIM:607681	Febrile seizures, familial, 8		HP:0002069	PMID:11326274	PCS		7/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-06]
OMIM:607681	Febrile seizures, familial, 8		HP:0010849	OMIM:607681	TAS					P	HPO:probinson[2012-07-20]
OMIM:607681	Febrile seizures, familial, 8		HP:0002373	PMID:11326274	PCS		13/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-06]
OMIM:607681	Febrile seizures, familial, 8		HP:0002121	OMIM:607681	TAS					P	HPO:probinson[2009-02-17]
OMIM:607681	Febrile seizures, familial, 8		HP:0011463	PMID:11326274	PCS					C	HPO:probinson[2012-07-16];HPO:probinson[2022-10-06]
OMIM:607681	Febrile seizures, familial, 8		HP:0003829	PMID:11326274	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:607681	Febrile seizures, familial, 8		HP:0002392	OMIM:607681	TAS					P	HPO:probinson[2009-02-17]
OMIM:607681	Febrile seizures, familial, 8		HP:0000006	PMID:11326274	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-10-06]
OMIM:616954	You-Hoover-Fong syndrome		HP:0003577	PMID:27132593	PCS		1/6			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0000365	PMID:27132593	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001156	PMID:27132593	PCS		3/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001250	PMID:27132593	PCS		1/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001252	PMID:27132593	PCS		4/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001251	PMID:27132593	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0003593	PMID:27132593	PCS		4/6			C	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0100704	PMID:27132593	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0030084	PMID:27132593	PCS		4/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001249	PMID:27132593	PCS		6/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0003623	PMID:27132593	PCS		1/6			C	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0002751	PMID:27132593	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001583	PMID:27132593	PCS		2/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0000252	PMID:27132593	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0000175	PMID:27132593	PCS		1/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001344	PMID:27132593	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001263	PMID:27132593	PCS		6/6		HP:0012829	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001680	PMID:27132593	PCS		1/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0410263	PMID:27132593	PCS		0/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0010775	PMID:27132593	PCS		1/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0000191	PMID:27132593	PCS		1/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0100022	PMID:27132593	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0011590	PMID:27132593	PCS		2/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0000749	PMID:27132593	PCS		3/6			P	HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0000767	PMID:27132593	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0000007	PMID:27132593	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:616954	You-Hoover-Fong syndrome		HP:0001257	PMID:27132593	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-03]
OMIM:122100	Meesmann corneal dystrophy 1		HP:0009926	OMIM:122100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:122100	Meesmann corneal dystrophy 1		HP:0001131	PMID:2217484	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-08-09]
OMIM:122100	Meesmann corneal dystrophy 1		HP:0003680	PMID:2217484	PCS					C	HPO:probinson[2009-02-17];HPO:probinson[2020-08-09]
OMIM:122100	Meesmann corneal dystrophy 1		HP:0000613	OMIM:122100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:122100	Meesmann corneal dystrophy 1		HP:0007663	OMIM:122100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:122100	Meesmann corneal dystrophy 1		HP:0000006	PMID:9171831	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2020-08-09]
OMIM:122100	Meesmann corneal dystrophy 1		HP:0007856	OMIM:122100	TAS					P	HPO:probinson[2009-02-17]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001882	PMID:23738510	PCS		5/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001263	PMID:23738510	PCS		2/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0002240	PMID:23738510	PCS		7/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0003593	PMID:23738510	PCS		5/7			C	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0010702	PMID:23738510	PCS		7/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001508	PMID:23738510	PCS		7/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0002719	PMID:23738510	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001903	PMID:23738510	PCS		7/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0000007	PMID:23738510	PCS					I	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001978	PMID:23738510	PCS		5/5			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001873	PMID:23738510	PCS		7/7			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001744	PMID:23738510	PCS		7/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0000105	PMID:23738510	PCS		7/7			P	HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0001875	PMID:23738510	PCS		7/7			P	HPO:skoehler[2013-09-10];HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0002028	PMID:23738510	PCS		7/7			P	HPO:probinson[2023-01-23]
OMIM:615285	Neutropenia, severe congenital, 5, autosomal recessive		HP:0003623	PMID:23738510	PCS		2/7			C	HPO:probinson[2023-01-23]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0003621	PMID:17347475	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0001670	PMID:17347475	PCS		2/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0005110	PMID:17347475	PCS		1/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0002094	PMID:17347475	PCS		1/8			P	HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0011713	PMID:17347475	PCS		1/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0012664	PMID:17347475	PCS		0/8			P	HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0012764	PMID:17347475	PCS		1/8			P	HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0001639	PMID:17347475	PCS		8/8			P	HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0001712	PMID:17347475	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0001962	PMID:17347475	PCS		4/8			P	HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0001279	PMID:17347475	PCS		1/8			P	HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0000006	PMID:17347475	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0004756	PMID:17347475	PCS		1/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-04]
OMIM:613838	Cardiomyopathy, familial hypertrophic, 16		HP:0001645	PMID:17347475	PCS		1/8			P	HPO:probinson[2022-07-04]
OMIM:215700	Citrullinemia, classic		HP:0001254	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0001297	OMIM:215700	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:215700	Citrullinemia, classic		HP:0001250	PMID:35433176	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:6000353	PMID:28111830	PCS		29/29			P	HPO:probinson[2024-02-27]
OMIM:215700	Citrullinemia, classic		HP:0001251	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0001394	OMIM:215700	TAS					P	HPO:skoehler[2015-12-30]
OMIM:215700	Citrullinemia, classic		HP:0002240	OMIM:215700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:215700	Citrullinemia, classic		HP:0003593	PMID:35433176	PCS		3/17			C	HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0002181	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0001508	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0000737	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0001987	PMID:35433176	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0001249	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0002038	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0003623	PMID:35433176	PCS		13/17			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0003621	PMID:35433176	PCS		1/17			C	HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0005961	OMIM:215700	TAS					P	HPO:probinson[2010-12-08]
OMIM:215700	Citrullinemia, classic		HP:0002013	PMID:35433176	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0001263	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0011966	PMID:35433176	PCS		15/15			P	HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0000007	PMID:7977368	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0001951	PMID:35433176	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0003217	PMID:35433176	PCS		14/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0003218	PMID:35433176	PCS		14/14			P	HPO:probinson[2012-07-22];HPO:probinson[2022-06-06]
OMIM:215700	Citrullinemia, classic		HP:0001950	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:215700	Citrullinemia, classic		HP:0001259	OMIM:215700	IEA					P	HPO:iea[2009-02-17]
OMIM:242880	Immunoerythromyeloid hypoplasia		HP:0008161	OMIM:242880	IEA					P	HPO:iea[2009-02-17]
OMIM:242880	Immunoerythromyeloid hypoplasia		HP:0005523	OMIM:242880	IEA					P	HPO:iea[2009-02-17]
OMIM:242880	Immunoerythromyeloid hypoplasia		HP:0012133	OMIM:242880	TAS					P	HPO:probinson[2013-04-12]
OMIM:242880	Immunoerythromyeloid hypoplasia		HP:0000007	OMIM:242880	IEA					I	HPO:iea[2009-02-17]
OMIM:242880	Immunoerythromyeloid hypoplasia		HP:0004315	OMIM:242880	IEA					P	HPO:iea[2009-02-17]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0007979	PMID:22901947	PCS		3/10			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0000486	PMID:31319223	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0002540	PMID:31319223	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0000640	PMID:31319223	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0004322	PMID:22901947	PCS	HP:0003581	7/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001310	PMID:31319223;PMID:22901947	PCS		11/11			P	HPO:probinson[2021-02-14];HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001250	PMID:22901947	PCS		2/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001272	PMID:31319223;PMID:22901947	PCS		8/8			P	HPO:probinson[2021-02-14];HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001271	PMID:22901947	PCS		1/7			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0002066	PMID:22901947	PCS		10/10			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0003593	PMID:22901947	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001251	PMID:31319223	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0007068	PMID:22901947	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0006951	PMID:22901947	PCS		5/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001249	PMID:22901947	PCS		10/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001347	PMID:22901947	PCS		9/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0008936	PMID:31319223	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0000571	PMID:22901947	PCS		4/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0000750	PMID:22901947	PCS		10/10			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001344	PMID:31319223	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001260	PMID:22901947	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0002198	PMID:22901947	PCS		4/7			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001263	PMID:22901947	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0002075	PMID:22901947	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0011344	PMID:31319223	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0012378	PMID:22901947	PCS		1/10			P	HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0000508	PMID:22901947	PCS		3/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0000007	PMID:22901947	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0007256	PMID:22901947	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0000565	PMID:22901947	PCS		4/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0001337	PMID:22901947	PCS		10/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-02-14]
OMIM:614831	Spinocerebellar ataxia, autosomal recessive 13		HP:0003677	PMID:22901947	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0002795	OMIM:242670	TAS					P	HPO:probinson[2012-03-26]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0002257	OMIM:242670	TAS					P	HPO:probinson[2012-03-26]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0012265	OMIM:242670	IEA					P	HPO:skoehler[2015-01-19]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0012267	OMIM:242670	TAS					P	HPO:probinson[2013-04-07]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0012263	OMIM:242670	TAS					P	HPO:probinson[2013-04-07]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0000007	OMIM:242670	TAS					I	HPO:probinson[2009-02-17]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0100582	OMIM:242670	TAS					P	HPO:probinson[2009-02-17]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0012208	OMIM:242670	TAS					P	HPO:probinson[2013-04-07]
OMIM:242670	Ciliary dyskinesia with defective radial spokes		HP:0000246	OMIM:242670	TAS					P	HPO:probinson[2009-02-17]
OMIM:611961	Stevenson-Carey syndrome		HP:0000463	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0001250	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000160	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0002020	OMIM:611961	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611961	Stevenson-Carey syndrome		HP:0005274	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0002280	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0002714	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0002019	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000358	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0001249	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000010	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000494	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0001385	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0002650	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000430	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0001321	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0002079	OMIM:611961	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611961	Stevenson-Carey syndrome		HP:0001263	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0012385	OMIM:611961	TAS					P	HPO:skoehler[2013-10-22]
OMIM:611961	Stevenson-Carey syndrome		HP:0009473	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0007110	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0011670	OMIM:611961	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611961	Stevenson-Carey syndrome		HP:0000007	OMIM:611961	IEA					I	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000568	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000201	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0001631	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000248	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000369	OMIM:611961	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611961	Stevenson-Carey syndrome		HP:0000589	OMIM:611961	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0001650	PMID:22539340	PCS		4/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0000594	PMID:22539340	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0004322	PMID:22539340	PCS		10/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0001387	PMID:22539340	PCS		5/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0001156	PMID:22539340	PCS		5/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0030961	PMID:22539340	PCS		3/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0007906	PMID:22539340	PCS		2/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0000007	PMID:22539340	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0001083	PMID:22539340	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0011003	PMID:22539340	PCS		3/12			P	HPO:probinson[2023-02-26]
OMIM:614819	Weill-Marchesani syndrome 3		HP:0001642	PMID:22539340	PCS		5/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-26]
OMIM:613810	Retinitis pigmentosa 43		HP:0007737	PMID:21039428	PCS		4/4			P	HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0000662	PMID:21039428	PCS	HP:0003621	4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0000580	PMID:21039428	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0000007	PMID:21039428	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-21]
OMIM:613810	Retinitis pigmentosa 43		HP:0000505	PMID:21039428	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0007994	PMID:21039428	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0000543	PMID:21039428	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0000510	PMID:21039428	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0007787	PMID:21039428	PCS		2/4			P	HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0007843	PMID:21039428	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2020-08-10]
OMIM:613810	Retinitis pigmentosa 43		HP:0000512	PMID:21039428	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-08-10]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0002046	PMID:30487221	PCS		2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0011968	PMID:30487221	PCS		2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0002572	PMID:30487221	PCS		2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0007110	PMID:30487221	PCS		2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0012450	PMID:30487221	PCS		2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0000007	PMID:30487221	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0002878	PMID:30487221	PCS	HP:0003623	2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0002104	PMID:30487221	PCS		2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0000875	PMID:30487221	PCS		2/2			P	HPO:probinson[2021-10-23]
OMIM:619483	Central hypoventilation syndrome, congenital, 3		HP:0003623	PMID:30487221	PCS		2/2			C	HPO:probinson[2021-10-23]
OMIM:214350	CHANDS		HP:0002212	OMIM:214350	IEA					P	HPO:iea[2009-02-17]
OMIM:214350	CHANDS		HP:0002164	OMIM:214350	IEA					P	HPO:iea[2009-02-17]
OMIM:214350	CHANDS		HP:0000007	OMIM:214350	IEA					I	HPO:iea[2009-02-17]
OMIM:214350	CHANDS		HP:0009755	OMIM:214350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:214350	CHANDS		HP:0002710	OMIM:214350	IEA					P	HPO:iea[2009-02-17]
OMIM:616968	Deafness, autosomal dominant 70		HP:0003621	PMID:26196677	PCS					C	HPO:probinson[2024-03-15]
OMIM:616968	Deafness, autosomal dominant 70		HP:0001751	PMID:26196677	PCS		0/8			P	HPO:probinson[2017-06-24];HPO:probinson[2024-03-15]
OMIM:616968	Deafness, autosomal dominant 70		HP:0000408	PMID:26196677	PCS		8/8			P	HPO:probinson[2017-06-24];HPO:probinson[2024-03-15]
OMIM:616968	Deafness, autosomal dominant 70		HP:0003581	PMID:26196677	PCS					C	HPO:probinson[2024-03-15]
OMIM:616968	Deafness, autosomal dominant 70		HP:0000006	PMID:26196677	PCS					I	HPO:probinson[2017-06-24]
OMIM:616968	Deafness, autosomal dominant 70		HP:0003677	PMID:26196677	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0000286	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0008936	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001344	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001695	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001250	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0002151	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001263	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0000470	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001251	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0011923	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001508	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0000007	PMID:23603806	PCS					I	HPO:probinson[2020-08-26];HPO:probinson[2022-12-03]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0008347	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0000218	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001324	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0000311	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0002500	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0000666	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0000369	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:618951	Combined oxidative phosphorylation deficiency 45		HP:0001337	PMID:23603806	PCS		1/1			P	HPO:probinson[2020-08-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000252	PMID:21358632	PCS		2/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0003577	PMID:21358632	PCS		7/7			C	HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0002750	PMID:21358632	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0004322	PMID:21358632	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0003561	PMID:21358632	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0003187	OMIM:613804	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0011968	PMID:21358632	PCS		2/4			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000160	PMID:21358632	PCS		2/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0003100	PMID:21358632	PCS		4/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0002097	PMID:21358632	PCS	HP:0003577	4/7			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0001508	OMIM:613804	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0002816	PMID:21358632	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0008551	PMID:21358632	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000327	PMID:21358632	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000007	PMID:21358632	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0006443	PMID:21358632	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0001511	OMIM:613804	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000895	OMIM:613804	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000179	PMID:21358632	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000028	PMID:21358632	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0001249	PMID:21358632	PCS		0/7			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000369	PMID:21358632	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613804	Meier-Gorlin syndrome 4		HP:0000347	PMID:21358632;OMIM:613804	PCS		16/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0012211	OMIM:123550	IEA					P	HPO:iea[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0001871	OMIM:123550	IEA					P	HPO:iea[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0000790	OMIM:123550	IEA					P	HPO:iea[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0100778	OMIM:123550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0000822	OMIM:123550	IEA					P	HPO:iea[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0000093	OMIM:123550	IEA					P	HPO:iea[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0012050	OMIM:123550	TAS					P	HPO:skoehler[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0000006	OMIM:123550	IEA					I	HPO:iea[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0003259	OMIM:123550	IEA					P	HPO:iea[2009-02-17]
OMIM:123550	Cryoglobulinemia, familial mixed		HP:0012622	OMIM:123550	TAS					P	HPO:skoehler[2014-05-04]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001696	PMID:36074124	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0002783	PMID:36074124	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0003363	PMID:36074124	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0003593	PMID:36074124	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0011567	PMID:36074124	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0004383	PMID:36074124	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0034315	PMID:36074124	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0011553	PMID:36074124	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0031565	PMID:36074124	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0005160	PMID:36074124	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001629	PMID:36074124	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0011463	PMID:36074124	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001719	PMID:36074124	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0011560	PMID:36074124	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001669	PMID:36074124	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0000403	PMID:36074124	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0000007	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001643	PMID:36074124	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001642	PMID:36074124	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001631	PMID:36074124	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:620570	Ciliary dyskinesia, primary, 52		HP:0001655	PMID:36074124	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0003577	PMID:18950742	PCS					C	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0000494	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0001762	PMID:18950742	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0004322	PMID:21775501	PCS		3/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0002079	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0003065	PMID:18950742	PCS		3/5			P	HPO:skoehler[2012-11-16];HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0002280	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0005280	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0009099	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0003829	PMID:18950742	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0010691	PMID:22258522	PCS	HP:0003577	2/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0003826	PMID:22258522	PCS		1/3			C	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0000316	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0009556	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0001841	PMID:18950742	PCS		1/6			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0009756	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0000006	PMID:18950742	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0000369	PMID:22258522	PCS		1/3			P	HPO:probinson[2021-02-20]
OMIM:119800	Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly		HP:0001776	PMID:21775501;PMID:22258522;PMID:18950742	PCS		11/12			P	HPO:probinson[2021-02-20]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0002003	PMID:23092983	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0000750	PMID:23092983	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0002376	PMID:23092983	PCS		0/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0000430	PMID:23092983	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0001250	PMID:23092983	PCS		0/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0001419	PMID:21865298	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0000160	PMID:23092983	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0000717	PMID:23092983	PCS		2/2			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0000508	PMID:23092983	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0000322	PMID:23092983	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0001249	PMID:23092983	PCS		2/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-02-21]
OMIM:300872	Autism, susceptibility to, X-linked 6		HP:0001513	PMID:23092983	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0030007	PMID:20428114	PCS		1/1			P	HPO:probinson[2022-06-19];HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0002015	PMID:20428114	PCS		4/8			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12		HP:0003676	PMID:20428114	PCS					C	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12		HP:0003596	PMID:20428114	PCS		5/8			C	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0001260	PMID:20428114	PCS		5/8			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12		HP:0003584	PMID:20428114	PCS		1/8			C	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0002380	PMID:20428114	PCS		1/8			P	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0012473	PMID:20428114	PCS		2/8			P	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12		HP:0011462	PMID:20428114	PCS		2/8			C	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0007354	PMID:20428114	PCS		8/8			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0000007	PMID:20428114	PCS					I	HPO:nvasilevsky[2019-03-12]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0002878	PMID:20428114	PCS		3/8			P	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0001308	PMID:20428114	PCS		4/8			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0002505	PMID:20428114	PCS		2/8			P	HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0001324	PMID:20428114	PCS		8/8			P	HPO:probinson[2013-06-02];HPO:probinson[2022-06-19]
OMIM:613435	Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia		HP:0000006	PMID:20428114	PCS					I	HPO:nvasilevsky[2019-03-12]
OMIM:277350	Vitamin A metabolic defect		HP:0000662	OMIM:277350	IEA					P	HPO:iea[2009-02-17]
OMIM:277350	Vitamin A metabolic defect		HP:0007462	OMIM:277350	IEA					P	HPO:iea[2009-02-17]
OMIM:277350	Vitamin A metabolic defect		HP:0004905	OMIM:277350	IEA					P	HPO:iea[2009-02-17]
OMIM:277350	Vitamin A metabolic defect		HP:0000007	OMIM:277350	IEA					I	HPO:iea[2009-02-17]
OMIM:277350	Vitamin A metabolic defect		HP:0007502	OMIM:277350	IEA					P	HPO:iea[2009-02-17]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000286	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000582	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000486	PMID:26986877	PCS		6/6			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0001212	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000463	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0001252	PMID:26986877	PCS		2/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0011261	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000639	PMID:26986877	PCS		4/6			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0100704	PMID:24462372	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000717	PMID:24462372	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0007663	PMID:26986877	PCS		6/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000218	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000411	PMID:26986877	PCS		2/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0002217	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000278	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0001249	PMID:24462372	PCS		4/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000154	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000395	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0001123	OMIM:615722	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0011968	PMID:26986877	PCS	HP:0003623	2/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0001263	PMID:26986877	PCS		19/20			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0009909	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0001182	PMID:26986877	PCS		2/6			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000426	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000722	PMID:24462372	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000648	PMID:26986877	PCS		15/20			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000307	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000543	PMID:24462372	PCS		5/6			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0001257	PMID:26986877	PCS		1/6			P	HPO:probinson[2022-08-20]
OMIM:615722	Bosch-Boonstra-Schaaf optic atrophy syndrome		HP:0000006	PMID:24462372	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-20]
OMIM:613353	Mononeuropathy of the median nerve, mild		HP:0003477	PMID:20220177	PCS		2/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-07]
OMIM:613353	Mononeuropathy of the median nerve, mild		HP:0012185	PMID:20220177	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:613353	Mononeuropathy of the median nerve, mild		HP:0003581	PMID:20220177	PCS					C	HPO:probinson[2022-10-07]
OMIM:613353	Mononeuropathy of the median nerve, mild		HP:0009831	OMIM:613353	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613353	Mononeuropathy of the median nerve, mild		HP:0000006	PMID:20220177	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-07]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0000882	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0001552	PMID:19005420	PCS		1/1			P	HPO:skoehler[2010-06-20]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0003311	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0001376	PMID:19005420	PCS		1/1			P	HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0004322	PMID:19005420	PCS		1/1			P	HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0002681	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0008829	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0003274	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0010049	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0011463	PMID:19005420	PCS		1/1			C	HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0002515	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0002857	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0001249	PMID:19005420	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0008835	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0009803	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0003521	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0003467	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0000252	PMID:19005420	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0002650	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0002970	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0003025	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0002692	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0000470	PMID:19005420	PCS		1/1			P	HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0002808	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0010582	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0000926	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0000007	PMID:12491225	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0008786	PMID:19005420	PCS		1/1			P	HPO:probinson[2023-04-14]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0000268	OMIM:607326	IEA					P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0000884	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:607326	Smith-Mccort dysplasia 1		HP:0004568	PMID:19005420	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0003016	OMIM:184260	TAS					P	HPO:probinson[2015-03-08]
OMIM:184260	Osteochondrodysplasia		HP:0002983	PMID:30728324	PCS		1/10			P	HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0000684	OMIM:184260	TAS					P	HPO:skoehler[2010-06-20]
OMIM:184260	Osteochondrodysplasia		HP:0000343	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0002089	PMID:30728324	PCS		4/10			P	HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0001156	PMID:30728324	PCS		10/10			P	HPO:skoehler[2018-10-08];HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0004322	PMID:30728324	PCS		9/10			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0010049	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0004482	OMIM:184260	IEA					P	HPO:skoehler[2019-04-18]
OMIM:184260	Osteochondrodysplasia		HP:0001270	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0010585	OMIM:184260	TAS					P	HPO:probinson[2012-06-18]
OMIM:184260	Osteochondrodysplasia		HP:0000939	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0010230	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0002816	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0011220	OMIM:184260	TAS					P	HPO:skoehler[2012-10-17]
OMIM:184260	Osteochondrodysplasia		HP:0000774	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0001522	PMID:30728324	PCS		3/10			C	HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0002657	PMID:30728324	PCS		10/10			P	HPO:skoehler[2015-01-27];HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0000256	PMID:30728324	PCS		10/10			P	HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0000113	OMIM:184260	IEA					P	HPO:skoehler[2019-04-18]
OMIM:184260	Osteochondrodysplasia		HP:0009803	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0000275	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0003026	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0003027	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0002650	PMID:30728324	PCS		5/10			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0002970	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0001382	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0002098	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0003021	OMIM:184260	TAS					P	HPO:probinson[2015-03-08]
OMIM:184260	Osteochondrodysplasia		HP:0000090	PMID:30728324	PCS		1/10			P	HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0003180	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0010582	OMIM:184260	TAS					P	HPO:probinson[2012-06-18]
OMIM:184260	Osteochondrodysplasia		HP:0000926	OMIM:184260	TAS	HP:0003623				P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0002869	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0000007	OMIM:184260	TAS					I	HPO:skoehler[2019-04-18]
OMIM:184260	Osteochondrodysplasia		HP:0003417	OMIM:184260	TAS	HP:0003623				P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0000703	PMID:30728324	PCS		7/10			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0000768	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0002205	PMID:30728324	PCS		1/10			P	HP:probinson[2019-03-14]
OMIM:184260	Osteochondrodysplasia		HP:0004625	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0001216	OMIM:184260	TAS					P	HPO:probinson[2009-02-17]
OMIM:184260	Osteochondrodysplasia		HP:0008845	PMID:30728324	PCS					P	HP:probinson[2019-03-14];HP:probinson[2019-03-14]
OMIM:611544	Cataract 17, multiple types		HP:0100018	OMIM:611544	TAS	HP:0003577				P	HPO:probinson[2013-04-01]
OMIM:611544	Cataract 17, multiple types		HP:0003577	PMID:12360425	PCS		8/8			C	HPO:probinson[2023-02-09]
OMIM:611544	Cataract 17, multiple types		HP:0000639	OMIM:611544	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611544	Cataract 17, multiple types		HP:0010693	PMID:12360425	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:611544	Cataract 17, multiple types		HP:0000482	OMIM:611544	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611544	Cataract 17, multiple types		HP:0000519	OMIM:611544	IEA					P	HPO:skoehler[2015-01-27]
OMIM:611544	Cataract 17, multiple types		HP:0000646	OMIM:611544	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:611544	Cataract 17, multiple types		HP:0000007	OMIM:611544	TAS					I	HPO:probinson[2013-01-09]
OMIM:611544	Cataract 17, multiple types		HP:0007663	OMIM:611544	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611544	Cataract 17, multiple types		HP:0000006	PMID:12360425	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:137900	Globulin anomaly involving beta (2a)-globulin		HP:0003256	OMIM:137900	TAS					P	HPO:probinson[2009-02-17]
OMIM:137900	Globulin anomaly involving beta (2a)-globulin		HP:0002715	OMIM:137900	IEA					P	HPO:iea[2009-02-17]
OMIM:137900	Globulin anomaly involving beta (2a)-globulin		HP:0000006	OMIM:137900	IEA					I	HPO:iea[2009-02-17]
OMIM:617121	Joubert syndrome 28		HP:0002553	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0003577	PMID:24886560	PCS		1/2			C	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000486	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000750	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000431	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0001382	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0002395	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0001260	PMID:24886560	PCS					P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0001263	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0001251	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000580	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0001290	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000639	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0011461	PMID:24886560	PCS		1/2			C	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000657	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000316	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000007	PMID:24886560	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0002419	PMID:24886560	PCS		2/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000337	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0000543	PMID:24886560	PCS		1/2			P	HPO:probinson[2021-02-01]
OMIM:617121	Joubert syndrome 28		HP:0001249	PMID:24886560	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:610896	Branchiootorenal syndrome 2		HP:0000110	OMIM:610896	TAS					P	HPO:probinson[2013-04-01]
OMIM:610896	Branchiootorenal syndrome 2		HP:0000384	OMIM:610896	TAS					P	HPO:probinson[2013-04-01]
OMIM:610896	Branchiootorenal syndrome 2		HP:0000365	OMIM:610896	TAS					P	HPO:probinson[2013-04-01]
OMIM:610896	Branchiootorenal syndrome 2		HP:0011332	OMIM:610896	TAS					P	HPO:probinson[2013-04-01]
OMIM:610896	Branchiootorenal syndrome 2		HP:0000083	OMIM:610896	TAS					P	HPO:probinson[2013-04-01]
OMIM:610896	Branchiootorenal syndrome 2		HP:0000006	OMIM:610896	TAS					I	HPO:probinson[2013-01-09]
OMIM:613347	Pancreatic cancer, susceptibility to, 2		HP:0002894	OMIM:613347	TAS					P	HPO:probinson[2013-01-09]
OMIM:144050	HYPERHEPARINEMIA		HP:0001892	OMIM:144050	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:144050	HYPERHEPARINEMIA		HP:0000006	OMIM:144050	IEA					I	HPO:iea[2009-02-17]
OMIM:616559	Noonan syndrome 9		HP:0002212	PMID:25795793	PCS		4/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000494	PMID:25795793	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0010726	PMID:25795793	PCS		1/2			P	HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0004322	PMID:25795793	PCS		2/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000072	PMID:25795793	PCS		1/5			P	HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0001263	PMID:25795793	PCS		2/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0001680	PMID:25795793	PCS		1/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000470	PMID:25795793	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0045075	PMID:25795793	PCS		4/5			P	HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0008151	PMID:25795793	PCS		2/2			P	HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0032152	PMID:25795793	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0001629	PMID:25795793	PCS		1/5			P	HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000508	PMID:25795793	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000316	PMID:25795793	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0001642	PMID:25795793	PCS		1/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000465	PMID:25795793	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000028	PMID:25795793	PCS		1/1	MALE		P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616559	Noonan syndrome 9		HP:0000006	PMID:25795793	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-22]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002168	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0000486	PMID:33851480	PCS		1/5			P	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0003596	PMID:33851480	PCS		3/5			C	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002188	PMID:33851480	PCS		1/5			P	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001332	PMID:33851480	PCS		1/5			P	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001272	PMID:33851480	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002066	PMID:33851480	PCS		5/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001251	PMID:33851480	PCS		5/5			P	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0010543	PMID:33851480	PCS		1/5			P	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0010526	OMIM:607454	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002080	PMID:33851480	PCS		2/5			P	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0100543	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0000639	PMID:33851480	PCS		2/5			P	HPO:skoehler[2014-04-13];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0011463	PMID:33851480	PCS		1/5			C	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0000718	OMIM:607454	TAS					P	HPO:skoehler[2015-01-04]
OMIM:607454	Spinocerebellar ataxia 21		HP:0000514	OMIM:607454	TAS					P	HPO:skoehler[2015-01-04]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001268	PMID:33851480	PCS		3/5			P	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001249	PMID:33851480	PCS		2/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0003623	PMID:33851480	PCS		1/5			C	HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001265	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001300	OMIM:607454	TAS					P	HPO:skoehler[2014-04-13]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002396	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001260	PMID:33851480	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0001263	PMID:33851480	PCS		2/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002174	PMID:33851480	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002073	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002070	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002071	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0100710	PMID:33851480	PCS		1/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0007792	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0002304	OMIM:607454	IEA					P	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0000741	OMIM:607454	TAS					P	HPO:skoehler[2015-01-04]
OMIM:607454	Spinocerebellar ataxia 21		HP:0000006	PMID:33851480	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-31]
OMIM:607454	Spinocerebellar ataxia 21		HP:0003677	OMIM:607454	IEA					C	HPO:iea[2009-02-17]
OMIM:607454	Spinocerebellar ataxia 21		HP:0007338	PMID:33851480	PCS		2/5			P	HPO:probinson[2021-05-31]
OMIM:109150	Machado-Joseph disease		HP:0003676	PMID:19659750	PCS					C	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002067	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000640	PMID:10525976	PCS		15/20			P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0001332	PMID:19659750	PCS		17/57			P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0001151	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0003693	OMIM:109150	TAS					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0001272	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0030454	OMIM:109150	TAS					P	HPO:skoehler[2015-12-30]
OMIM:109150	Machado-Joseph disease		HP:0002063	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0003394	OMIM:109150	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109150	Machado-Joseph disease		HP:0001251	PMID:19659750	PCS		57/57			P	HPO:iea[2010-09-09]
OMIM:109150	Machado-Joseph disease		HP:0002380	PMID:19659750	PCS		12/57			P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0012332	OMIM:109150	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002839	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0007089	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0025710	PMID:19659750	PCS					C	HPO:probinson[2022-06-24]
OMIM:109150	Machado-Joseph disease		HP:0003743	OMIM:109150	IEA					I	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002015	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000651	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002078	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0001300	PMID:19659750	PCS		3/57			P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0003487	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002495	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002198	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0001260	PMID:19659750	PCS		30/57			P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002171	OMIM:109150	TAS					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002073	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002172	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002070	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002071	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0012532	OMIM:109150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:109150	Machado-Joseph disease		HP:0000726	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000508	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000623	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000520	OMIM:109150	TAS					P	HPO:probinson[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000641	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0002503	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0003438	OMIM:109150	IEA					P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0001257	PMID:18685131	PCS		62/139			P	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000006	OMIM:109150	TAS					I	HPO:iea[2009-02-17]
OMIM:109150	Machado-Joseph disease		HP:0000544	PMID:19659750	PCS		34/57			P	HPO:iea[2009-02-17]
OMIM:612717	Myopia 15		HP:0000006	OMIM:612717	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612717	Myopia 15		HP:0000545	OMIM:612717	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0008162	PMID:10636977	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0001508	PMID:10636977	PCS		4/5			P	HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0000825	PMID:10636977	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0002173	PMID:10636977	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0003593	PMID:10636977	PCS		3/5			C	HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0006476	PMID:10636977	PCS		0/5			P	HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0000006	PMID:10636977	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0001249	PMID:10636977	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0001325	PMID:10636977	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:606762	Hyperinsulinemic hypoglycemia, familial, 6		HP:0003623	PMID:10636977	PCS		2/5			C	HPO:probinson[2022-09-02]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0001771	PMID:18179888	PCS		9/9			P	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003202	PMID:18179888	PCS		9/9			P	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003236	PMID:18179888	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003676	PMID:18179888	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0002650	PMID:18179888	PCS		9/9			P	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003089	PMID:18179888	PCS		9/9			P	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003691	PMID:18179888	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0005991	PMID:18179888	PCS		9/9			P	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0000470	PMID:18179888	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0011675	PMID:18179888	PCS		1/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0002093	PMID:18179888	PCS		2/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0001639	PMID:18179888	PCS		4/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0001419	PMID:18179888	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0011462	PMID:18179888	PCS		9/9			C	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003805	OMIM:300696	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003418	PMID:18179888	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003704	PMID:18179888	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003701	PMID:18179888	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003712	PMID:18179888	PCS		9/9			P	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003306	PMID:18179888	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003458	PMID:18179888	PCS		7/8			P	HPO:probinson[2022-09-26]
OMIM:300696	Myopathy, X-linked, with postural muscle atrophy		HP:0003557	PMID:18179888	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0001265	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0003444	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0003477	OMIM:610100	IEA					P	HPO:skoehler[2015-01-27]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0003376	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0003431	OMIM:610100	TAS				HP:0012825	P	HPO:probinson[2012-04-28]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0001761	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0006937	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0003693	OMIM:610100	TAS					P	HPO:probinson[2012-04-28]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0003383	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0001284	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0002460	OMIM:610100	TAS					P	HPO:probinson[2012-04-28]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0001638	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0006886	OMIM:610100	TAS					P	HPO:probinson[2012-04-28]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0000006	OMIM:610100	IEA					I	HPO:iea[2009-02-17]
OMIM:610100	Giant axonal neuropathy, autosomal dominant		HP:0001765	OMIM:610100	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0002312	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0003577	OMIM:608029	IEA					C	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0000750	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001310	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0004322	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001272	OMIM:608029	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0002066	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001252	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0003680	OMIM:608029	IEA					C	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001251	OMIM:608029	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001290	OMIM:608029	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001270	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0002080	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0000007	OMIM:608029	IEA					I	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001257	OMIM:608029	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001763	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:608029	Spinocerebellar ataxia, autosomal recessive 6		HP:0001347	OMIM:608029	IEA					P	HPO:iea[2009-02-17]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001276	PMID:32282878	PCS		3/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0002487	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0002521	PMID:32282878	PCS		2/10			P	HPO:probinson[2021-01-04];HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000582	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000343	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001332	PMID:32282878	PCS		3/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000463	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001371	PMID:32282878	PCS		6/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001272	PMID:32282878	PCS		2/9			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000064	PMID:32282878	PCS		1/5	FEMALE		P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0003593	PMID:32282878	PCS		1/11			C	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0032794	PMID:32282878	PCS		6/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0012368	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0045075	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0010722	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000319	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000316	PMID:32282878	PCS		4/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000219	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04];HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000059	PMID:32282878	PCS		1/5	FEMALE		P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000774	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000256	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0003623	PMID:32282878	PCS		10/11			C	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001347	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0008936	PMID:32282878	PCS		5/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0002553	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000175	PMID:32282878	PCS		7/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0002059	PMID:32282878	PCS		2/9			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000494	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0009826	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0002650	PMID:32282878	PCS		4/11			P	HPO:probinson[2021-01-04];HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001762	PMID:32282878	PCS		5/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000431	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0002079	PMID:32282878	PCS		1/9			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001263	PMID:32282878	PCS		7/7			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0002273	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0025190	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0010851	PMID:32282878	PCS		7/10			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0005280	PMID:32282878	PCS		1/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0011097	PMID:32282878	PCS		6/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0003819	PMID:32282878	PCS		3/11			C	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000308	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000007	PMID:32282878	PCS					I	HPO:probinson[2021-01-04];HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001539	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0008665	PMID:32282878	PCS		1/5	FEMALE		P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0003811	PMID:32282878	PCS		1/11			C	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0001257	PMID:32282878	PCS		5/11			P	HPO:probinson[2021-01-04]
OMIM:619124	Developmental and epileptic encephalopathy 89		HP:0000369	PMID:32282878	PCS		2/11			P	HPO:probinson[2021-01-04]
OMIM:616217	Nephronophthisis 19		HP:0003774	PMID:25557784	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0001396	PMID:25557784	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0032948	PMID:25557784	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0001408	PMID:25557784	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0001395	PMID:25557784	PCS		1/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0002240	PMID:25557784	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0004719	PMID:25557784	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0003593	PMID:25557784	PCS		2/2			C	HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0000090	PMID:25557784	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0000007	PMID:25557784	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0006563	PMID:25557784	PCS		1/2			P	HPO:probinson[2023-03-29]
OMIM:616217	Nephronophthisis 19		HP:0001744	PMID:25557784	PCS		2/2			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-03-29]
OMIM:108500	Episodic ataxia, type 2		HP:0003401	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0000640	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0001751	OMIM:108500	TAS					P	HPO:probinson[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0000651	OMIM:108500	IEA					P	HPO:skoehler[2012-10-12]
OMIM:108500	Episodic ataxia, type 2		HP:0002321	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0002486	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0001332	OMIM:108500	TAS					P	HPO:probinson[2012-04-11]
OMIM:108500	Episodic ataxia, type 2		HP:0002076	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0002131	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0001260	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0000360	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0001152	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0002073	OMIM:108500	IEA					P	HPO:skoehler[2012-10-12]
OMIM:108500	Episodic ataxia, type 2		HP:0010545	OMIM:108500	IEA					P	HPO:skoehler[2012-10-12]
OMIM:108500	Episodic ataxia, type 2		HP:0003829	OMIM:108500	IEA					I	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0001324	OMIM:108500	TAS					P	HPO:probinson[2012-04-11]
OMIM:108500	Episodic ataxia, type 2		HP:0000006	OMIM:108500	IEA					I	HPO:iea[2009-02-17]
OMIM:108500	Episodic ataxia, type 2		HP:0006855	OMIM:108500	IEA					P	HPO:iea[2009-02-17]
OMIM:614414	Deafness, autosomal recessive 96		HP:0000365	OMIM:614414	TAS					P	HPO:skoehler[2015-01-21]
OMIM:614414	Deafness, autosomal recessive 96		HP:0000007	OMIM:614414	TAS					I	HPO:skoehler[2012-10-17]
OMIM:276700	Tyrosinemia, type I		HP:0000121	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0003235	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0001399	PMID:33046095	PCS		18/18			P	HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0003231	PMID:33046095	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0000083	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0006949	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:6000598	PMID:23311542	PCS					P	HPO:probinson[2024-04-03]
OMIM:276700	Tyrosinemia, type I		HP:0002240	PMID:33046095	PCS		10/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0001394	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:6000775	PMID:20301688	PCS					P	HPO:probinson[2024-06-29]
OMIM:276700	Tyrosinemia, type I		HP:0008151	OMIM:276700	TAS					P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0001508	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0001903	PMID:33046095	PCS		8/18			P	HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0006254	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0001943	PMID:33046095	PCS		9/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0001945	PMID:33046095	PCS		9/18			P	HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0006554	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0004912	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0003768	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0002239	OMIM:276700	TAS					P	HPO:probinson[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0002910	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0001744	PMID:33046095	PCS		6/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0001942	PMID:33046095	PCS		12/18			P	HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0001402	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0003645	OMIM:276700	TAS					P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0004510	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0001541	PMID:33046095	PCS		9/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0002572	PMID:33046095	PCS		7/18			P	HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0003163	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0000096	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0002590	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:6000827	PMID:6622096	PCS		9/9			P	HPO:probinson[2024-08-03]
OMIM:276700	Tyrosinemia, type I		HP:0001639	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0000007	PMID:8028615	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0002249	PMID:33046095	PCS		5/18			P	HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0001994	OMIM:276700	IEA					P	HPO:iea[2009-02-17]
OMIM:276700	Tyrosinemia, type I		HP:0001510	PMID:33046095	PCS		12/18			P	HPO:probinson[2022-08-27]
OMIM:276700	Tyrosinemia, type I		HP:0000105	PMID:33046095	PCS		10/17			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-08-27]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0011891	PMID:31217188	PCS		1/5	FEMALE		P	HPO:probinson[2021-01-10]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0011870	PMID:31217188	PCS		2/5			P	HPO:probinson[2021-01-10]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0011871	PMID:31217188	PCS		1/5			P	HPO:probinson[2021-01-10]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0008320	PMID:31217188	PCS		2/5			P	HPO:probinson[2021-01-10]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0033536	PMID:31217188	PCS		7/7			P	HPO:probinson[2021-02-13]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0001873	PMID:31217188	PCS		23/23			P	HPO:probinson[2021-01-10]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0033535	PMID:31217188	PCS		2/2			P	HPO:probinson[2021-02-13]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0000006	PMID:31217188	PCS					I	HPO:probinson[2021-01-10];HPO:probinson[2021-01-10]
OMIM:619130	Thrombocytopenia, autosomal dominant, 7		HP:0004866	PMID:31217188	PCS		2/5			P	HPO:probinson[2021-01-10]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0003596	PMID:29967133	PCS		1/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0010648	PMID:29967133	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0004322	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0010809	PMID:29967133	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0010886	PMID:26247899	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0012432	PMID:26247899	PCS		2/4			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0012393	PMID:26247899	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0011463	PMID:29967133	PCS		1/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0011462	PMID:29967133	PCS		2/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002619	PMID:26247899;PMID:29967133	PCS		4/12			P	HPO:probinson[2022-02-19];HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001647	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000316	PMID:26247899;PMID:29967133	PCS		4/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001763	PMID:26247899;PMID:29967133	PCS		3/10			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000494	PMID:29967133	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000098	PMID:30157302;PMID:29967133	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0005302	PMID:26247899	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001382	PMID:30157302;PMID:26247899	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002076	PMID:26247899;PMID:29967133	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001065	PMID:26247899;PMID:29967133	PCS		3/9			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0011800	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0012385	PMID:26247899	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002829	PMID:26247899;PMID:29967133	PCS		7/11			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0033981	PMID:26247899	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001537	PMID:26247899	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000766	PMID:26247899;PMID:28283438;PMID:29967133	PCS		3/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002108	PMID:29967133	PCS		0/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0008843	PMID:26247899	PCS		1/2			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000006	PMID:26247899	PCS					I	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002960	PMID:26247899	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0005116	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0003577	PMID:29967133	PCS		1/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000023	PMID:26247899;PMID:29967133	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0012727	PMID:26247899;PMID:28283438;PMID:29967133	PCS		10/15			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0005112	PMID:28283438;PMID:29967133	PCS		1/11			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000978	PMID:26247899;PMID:29967133	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000218	PMID:30157302;PMID:28283438;PMID:26247899;PMID:29967133	PCS		6/16			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002758	PMID:26247899	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000977	PMID:26247899	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000776	PMID:29967133	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001166	PMID:26247899;PMID:29967133	PCS		6/14			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0008419	PMID:26247899;PMID:28283438	PCS		3/4			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002650	PMID:26247899;PMID:29967133	PCS		5/12			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000276	PMID:28283438	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000193	PMID:26247899;PMID:29967133	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0003584	PMID:29967133	PCS		1/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0003581	PMID:28283438	PCS		1/1			C	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0005086	PMID:26247899	PCS		1/2			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0012158	PMID:26247899;PMID:29967133	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001519	PMID:26247899	PCS		1/4			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0012163	PMID:26247899	PCS		1/3			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0034179	PMID:26247899	PCS		1/3			P	HPO:probinson[2022-04-15]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0001714	PMID:26247899	PCS		1/3			P	HPO:probinson[2022-02-19]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0006687	PMID:26247899	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0000268	PMID:28283438;PMID:29967133	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0002326	PMID:29967133	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:619656	Loeys-Dietz syndrome 6		HP:0004944	PMID:30157302;PMID:26247899;PMID:29967133	PCS		3/11			P	HPO:probinson[2022-02-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0002421	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0008947	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000483	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000343	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000463	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000023	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000260	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0003155	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0032794	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0010544	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000280	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0009023	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0100704	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000319	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0008872	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0002119	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0001869	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000219	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0002714	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000977	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000455	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0001540	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0001561	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000076	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0002650	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000293	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0009909	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0030822	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000803	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000506	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0031165	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000508	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000767	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000007	PMID:31148362	PCS					I	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0001357	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000347	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618548	Epileptic encephalopathy, early infantile, 77		HP:0000522	PMID:31148362	PCS		1/1			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:272200	Multiple sulfatase deficiency		HP:0002003	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0007957	OMIM:272200	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:272200	Multiple sulfatase deficiency		HP:0000365	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0004322	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0000463	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0001272	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0001251	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0002240	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0000280	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0012368	OMIM:272200	TAS					P	HPO:skoehler[2013-10-22]
OMIM:272200	Multiple sulfatase deficiency		HP:0010055	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0011220	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0008155	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0000238	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0002518	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0002119	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0008479	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0001249	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0007305	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0001744	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0007307	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0002059	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0002395	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0001263	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0011304	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0011096	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0008064	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0100539	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0000943	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0000007	OMIM:272200	IEA					I	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0000546	OMIM:272200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0002922	OMIM:272200	IEA					P	HPO:iea[2009-02-17]
OMIM:272200	Multiple sulfatase deficiency		HP:0001319	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:272200	Multiple sulfatase deficiency		HP:0001257	OMIM:272200	TAS					P	HPO:probinson[2012-06-03]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0001650	OMIM:220220	TAS				HP:0012825	P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0006824	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000639	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000238	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000931	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0001305	OMIM:220220	TAS					P	HPO:probinson[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0002617	OMIM:220220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000933	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0001643	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000256	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000930	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0002951	OMIM:220220	TAS					P	HPO:probinson[2012-06-10]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0002335	OMIM:220220	TAS					P	HPO:probinson[2012-06-10]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000533	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0002078	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000431	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0001162	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0002198	OMIM:220220	IEA					P	HPO:iea[2009-02-17]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0045025	OMIM:220220	TAS					P	HPO:skoehler[2014-11-27]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0005280	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000627	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000308	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000007	OMIM:220220	TAS					I	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0002007	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000268	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:220220	Dandy-Walker malformation with postaxial polydactyly		HP:0000369	OMIM:220220	TAS					P	HPO:skoehler[2013-07-30]
OMIM:614372	Mannose-Binding lectin deficiency		HP:0001508	PMID:769701	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:614372	Mannose-Binding lectin deficiency		HP:0005353	PMID:7707811	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:614372	Mannose-Binding lectin deficiency		HP:0001581	PMID:7707811	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:614372	Mannose-Binding lectin deficiency		HP:0005381	PMID:7707811	PCS					P	HPO:lccarmody[2018-10-02];HPO:lccarmody[2018-10-02]
OMIM:614372	Mannose-Binding lectin deficiency		HP:0031699	PMID:7707811	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:614372	Mannose-Binding lectin deficiency		HP:0000006	OMIM:614372	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614372	Mannose-Binding lectin deficiency		HP:0002742	PMID:7707811	PCS					P	HPO:lccarmody[2018-10-02];HPO:lccarmody[2018-10-02]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0000340	PMID:25218063	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0003577	PMID:25218063;PMID:19215732	PCS		14/14			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0001344	PMID:25218063	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0001250	PMID:25218063	PCS		0/3			P	HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0001263	PMID:25218063;PMID:19215732	PCS		11/11			P	HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0011451	PMID:25218063;PMID:19215732	PCS		11/11			P	HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0000448	PMID:25218063	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0000007	PMID:19215732	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0001249	PMID:19215732	PCS		8/8			P	HPO:probinson[2013-04-06];HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0006315	PMID:25218063	PCS		0/3			P	HPO:probinson[2022-11-07]
OMIM:612703	Microcephaly 7, primary, autosomal recessive		HP:0009879	PMID:25218063	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-07]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002421	PMID:22101682	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0003577	PMID:22101682	PCS		5/10			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0010628	PMID:22101682	PCS		6/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0003236	PMID:22101682	PCS		0/7			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001250	PMID:22101682	PCS		2/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0100490	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001252	PMID:22101682	PCS		10/10			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002020	PMID:22101682	PCS		3/10			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001270	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001508	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0040131	PMID:22101682	PCS		0/9			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0009046	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0011461	PMID:22101682	PCS		5/10			C	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0006597	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002878	PMID:22101682	PCS		8/10			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001308	PMID:22101682	PCS		1/8			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0000218	PMID:22101682	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001265	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0000175	PMID:22101682	PCS		1/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002015	PMID:22101682	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002650	PMID:22101682	PCS		8/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001762	PMID:22101682	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002098	PMID:22101682	PCS		10/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001284	PMID:22101682	PCS		6/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002093	PMID:22101682	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0002091	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0009110	PMID:22101682	PCS		6/9			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0009113	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0000767	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0000007	PMID:22101682	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001558	PMID:22101682	PCS	HP:0011461	5/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001319	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0003713	PMID:22101682	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0001611	OMIM:614399	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0003458	PMID:22101682	PCS		6/7			P	HPO:probinson[2022-03-27]
OMIM:614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset		HP:0003557	PMID:22101682	PCS		6/7			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:617690	Ovarian dysgenesis 5		HP:0003621	PMID:25774885	PCS		3/4			C	HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0000013	PMID:25774885	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0025708	PMID:25774885	PCS		1/4			C	HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0004322	PMID:25774885	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0002750	PMID:25774885	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0011969	PMID:25774885	PCS		4/4			P	HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0008232	PMID:25774885	PCS		4/4			P	HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0000007	PMID:25774885	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0008214	PMID:25774885	PCS		3/4			P	HPO:probinson[2023-02-17]
OMIM:617690	Ovarian dysgenesis 5		HP:0000786	PMID:25774885	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-17]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001298	OMIM:607483	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001276	OMIM:607483	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002300	PMID:20065143	PCS		1/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001254	PMID:9679779	PCS		6/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0010628	PMID:9679779	PCS		3/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002345	PMID:9679779	PCS		3/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002540	OMIM:607483	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001332	PMID:9679779;PMID:26863430;PMID:20065143	PCS		15/15			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001250	PMID:9679779;PMID:26863430;PMID:20065143	PCS		10/15			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002066	PMID:20065143	PCS		1/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002385	OMIM:607483	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002063	OMIM:607483	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002062	OMIM:607483	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0012179	OMIM:607483	TAS					P	HPO:skoehler[2015-10-05]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0000639	OMIM:607483	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0000737	OMIM:607483	TAS					P	HPO:skoehler[2015-02-22]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0011463	PMID:26863430	IEA		3/3			C	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0011462	PMID:20065143	PCS		1/2			C	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001945	OMIM:607483	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002359	PMID:26863430	PCS		1/3			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0008936	OMIM:607483	TAS					P	HPO:skoehler[2015-02-22]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002179	PMID:9679779	PCS		3/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002015	PMID:20065143	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0003621	PMID:20065143;OMIM:607483	PCS		11/12			C	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001289	PMID:9679779;PMID:20065143	PCS		8/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002134	PMID:9679779	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0003487	PMID:9679779	PCS		5/10			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002013	PMID:9679779	PCS		5/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0030147	PMID:9679779	PCS		2/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002376	PMID:26863430	PCS		3/3			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001260	PMID:9679779	PCS		8/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002396	PMID:9679779	PCS		9/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001263	OMIM:607483	TAS		2/20			P	HPO:skoehler[2019-02-22];HPO:skoehler[2015-02-22]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002371	PMID:20065143	PCS		2/2			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002273	PMID:9679779	PCS		6/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0002072	PMID:9679779	PCS		2/10			P	HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0000508	PMID:20065143	PCS		1/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0007256	PMID:20065143	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0000007	PMID:15871139	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0001259	PMID:9679779	PCS		10/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-27]
OMIM:607483	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)		HP:0000544	OMIM:607483	IEA					P	HPO:skoehler[2010-06-19]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000771	OMIM:601794	IEA					P	HPO:iea[2009-02-17]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000518	OMIM:601794	IEA					P	HPO:iea[2009-02-17]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000480	OMIM:601794	TAS					P	HPO:skoehler[2013-03-13]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0100702	OMIM:601794	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000238	OMIM:601794	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000568	OMIM:601794	IEA					P	HPO:iea[2009-02-17]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000510	OMIM:601794	IEA					P	HPO:iea[2009-02-17]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000135	OMIM:601794	IEA					P	HPO:iea[2009-02-17]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000028	OMIM:601794	IEA					P	HPO:iea[2009-02-17]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0001513	OMIM:601794	IEA					P	HPO:iea[2009-02-17]
OMIM:601794	Coloboma-Obesity-Hypogenitalism-Impaired intellectual development syndrome		HP:0000006	OMIM:601794	TAS					I	HPO:skoehler[2013-05-29]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0003577	PMID:1867198	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001058	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001476	PMID:1867198	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001252	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001075	PMID:1867198	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001290	OMIM:130060	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0005191	PMID:1867198	PCS	HP:0003577	1/1			P	HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0009540	PMID:1867198	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0000938	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001822	PMID:1867198	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0000978	PMID:1867198	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0002659	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001027	PMID:1867198	PCS		1/1			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001763	PMID:1867198	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001623	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0000974	PMID:1867198	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0003502	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0002650	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0001382	PMID:1867198	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0003088	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0000272	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0002194	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0011800	OMIM:130060	TAS					P	HPO:skoehler[2013-11-28]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0009471	PMID:1867198	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0008780	PMID:1867198	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0032153	OMIM:130060	IEA					P	HPO:skoehler[2019-09-07]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0002808	OMIM:130060	IEA					P	HPO:iea[2009-02-17]
OMIM:130060	Ehlers-Danlos syndrome, arthrochalasia type, 1		HP:0000006	PMID:2767050	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:613390	Fanconi anemia, complementation group O		HP:0025023	PMID:20400963	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0003774	PMID:20400963	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0003577	PMID:20400963	PCS		3/3			C	HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0002023	PMID:20400963	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0001245	PMID:20400963	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0004322	PMID:20400963	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0005268	PMID:20400963	PCS		1/4			C	HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0003241	PMID:20400963	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0040012	PMID:20400963	PCS		2/2			P	HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0000107	PMID:20400963	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0000007	PMID:20400963	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0001627	PMID:20400963	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0009777	PMID:20400963	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0009623	PMID:20400963	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0003811	PMID:20400963	PCS		1/3			C	HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0001522	PMID:20400963	PCS		1/3			C	HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0009778	PMID:20400963	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0000028	PMID:20400963	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0002984	PMID:20400963	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:613390	Fanconi anemia, complementation group O		HP:0000126	PMID:20400963	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:211770	Cahmr syndrome		HP:0004554	OMIM:211770	IEA					P	HPO:iea[2009-02-17]
OMIM:211770	Cahmr syndrome		HP:0000007	OMIM:211770	IEA					I	HPO:iea[2009-02-17]
OMIM:211770	Cahmr syndrome		HP:0007971	OMIM:211770	IEA					P	HPO:iea[2009-02-17]
OMIM:211770	Cahmr syndrome		HP:0001249	OMIM:211770	IEA					P	HPO:iea[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000483	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002023	PMID:21165303;PMID:23304577	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000365	PMID:31337854;PMID:30246735	PCS		6/23			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000486	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000089	OMIM:122470	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0004322	PMID:31337854;PMID:36777704;PMID:38284454;PMID:22241092	PCS		33/38			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002021	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000086	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000482	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0003196	PMID:21165303;PMID:36777704;PMID:32074972;PMID:38284454	PCS		9/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002020	PMID:21165303;PMID:31337854;PMID:20358602;PMID:22241092	PCS		25/40			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000085	PMID:20358602	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0003593	PMID:36777704	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000639	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0008897	PMID:36777704;PMID:32074972;PMID:25447906;PMID:22241092;PMID:20358602;PMID:38284454	PCS		29/30			P	ORCID:0000-0002-0736-9199[2024-11-23];ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0009623	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:22241092;PMID:20358602;PMID:38284454	PCS		20/47			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000879	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0003745	OMIM:122470	IEA					I	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002036	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002553	PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:38284454;PMID:22241092	PCS		36/38			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000252	PMID:31337854;PMID:36777704;PMID:32074972;PMID:25447906;PMID:38284454;PMID:22241092	PCS		39/46			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002033	PMID:23304577	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0004691	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000093	OMIM:122470	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0003083	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000407	PMID:20358602;PMID:22241092;PMID:38284454	PCS		10/25			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000527	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:30246735;PMID:22241092;PMID:38284454	PCS		42/44			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000648	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0004209	PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:38284454;PMID:22241092	PCS		23/39			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000405	OMIM:122470	TAS					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0005815	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0007678	PMID:22241092	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000520	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000006	PMID:25447906	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-07-07]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000248	PMID:36777704;PMID:38284454	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-11-23];HPO:probinson[2012-05-01];HPO:probinson[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000369	PMID:21165303;PMID:32074972;PMID:25447906;PMID:38284454;PMID:22241092	PCS		9/19			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001612	PMID:23304577	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000126	PMID:23304577	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0003997	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001276	PMID:21165303;PMID:30246735	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-23];HPO:skoehler[2012-10-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000341	PMID:22241092	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0003577	PMID:21165303;PMID:23304577;PMID:30246735;PMID:32074972	PCS		6/6			C	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000343	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:25447906;PMID:22241092;PMID:38284454	PCS		37/46			P	ORCID:0000-0002-0736-9199[2024-11-23];HPO:probinson[2009-02-17];HPO:probinson[2024-07-07]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0004785	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000463	PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:22241092;PMID:38284454	PCS		32/41			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001156	PMID:20358602	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002120	PMID:20358602	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0004383	PMID:31337854;PMID:30246735	PCS		0/24			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001270	PMID:22241092	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000739	PMID:31337854	PCS		14/19			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0011120	PMID:36777704;PMID:32074972	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000733	PMID:36777704	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000219	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:30246735;PMID:32074972;PMID:25447906;PMID:22241092;PMID:38284454	PCS		36/44			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0030084	PMID:20358602	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0007665	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:25447906;PMID:38284454	PCS		33/39			P	ORCID:0000-0002-0736-9199[2024-11-23];HPO:probinson[2012-03-02]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000218	PMID:31337854;PMID:30246735;PMID:32074972;PMID:22241092;PMID:38284454;PMID:20358602	PCS		12/47			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000455	PMID:21165303;PMID:36777704;PMID:38284454	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000059	PMID:20358602	PCS		1/11			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001545	PMID:21165303;PMID:20358602	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000076	OMIM:122470	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000750	PMID:31337854;PMID:36777704;PMID:25447906;PMID:22241092;PMID:20358602	PCS		29/35			P	ORCID:0000-0002-0736-9199[2024-11-23];HPO:skoehler[2012-10-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0009829	PMID:23304577;PMID:31337854;PMID:32074972;PMID:22241092	PCS		1/34			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000470	PMID:31337854;PMID:30246735	PCS		14/24			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002090	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0012165	PMID:21165303;PMID:31337854;PMID:36777704;PMID:32074972;PMID:22241092;PMID:38284454;PMID:20358602	PCS		12/53			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000508	PMID:23304577;PMID:31337854;PMID:36777704;PMID:22241092	PCS		3/32			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000107	PMID:20358602	PCS		1/11			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0008743	PMID:23304577	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0100716	PMID:31337854;PMID:36777704	PCS		13/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001159	PMID:21165303;PMID:20358602	PCS		5/12			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0007018	PMID:31337854	PCS		16/19			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000347	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:38284454;PMID:22241092;PMID:20358602	PCS		27/46			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000588	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002983	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001770	PMID:23304577;PMID:32074972;PMID:22241092	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002188	PMID:32074972	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000684	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001377	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:22241092	PCS		12/34			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001773	PMID:38284454;PMID:22241092	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001250	PMID:21165303;PMID:31337854;PMID:32074972;PMID:20358602	PCS		12/37			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001252	PMID:20358602	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0410030	PMID:21165303;PMID:23304577;PMID:31337854	PCS		0/25			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0009380	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0031228	PMID:19764039	IEA					P	HP:probinson[2019-01-22]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000319	PMID:23304577;PMID:36777704;PMID:32074972;PMID:38284454;PMID:22241092	PCS		15/19			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000718	PMID:31337854	PCS		11/19			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001647	PMID:31337854;PMID:30246735	PCS		0/24			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000954	PMID:31337854;PMID:25447906;PMID:22241092	PCS		20/32			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001643	PMID:30246735	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001642	PMID:31337854;PMID:30246735;PMID:22241092;PMID:20358602	PCS		6/41			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001007	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:30246735;PMID:32074972;PMID:25447906;PMID:22241092;PMID:38284454;PMID:20358602	PCS		39/56			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001249	PMID:31337854;PMID:36777704;PMID:25447906;PMID:22241092;PMID:38284454;PMID:20358602	PCS		34/40			P	ORCID:0000-0002-0736-9199[2024-11-23];HPO:skoehler[2012-10-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000175	PMID:21165303;PMID:23304577;PMID:31337854;PMID:30246735;PMID:25447906;PMID:20358602;PMID:22241092	PCS		7/46			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000453	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0030148	PMID:20358602	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000574	PMID:21165303;PMID:23304577;PMID:36777704;PMID:30246735;PMID:38284454	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002750	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0011968	PMID:21165303;PMID:36777704;PMID:30246735;PMID:22241092;PMID:20358602	PCS		11/19			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000050	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001263	PMID:31337854;PMID:36777704;PMID:32074972;PMID:20358602;PMID:22241092	PCS		42/46			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000294	PMID:23304577;PMID:36777704;PMID:32074972;PMID:38284454;PMID:22241092	PCS		12/16			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0012385	PMID:20358602	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000729	PMID:31337854;PMID:36777704;PMID:22241092	PCS		9/25			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000965	PMID:22241092	PCS		4/6			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002987	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000047	PMID:32074972	PCS		1/3			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000204	OMIM:122470	TAS					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002984	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001655	PMID:30246735;PMID:22241092;PMID:20358602	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000687	PMID:31337854;PMID:38284454;PMID:22241092	PCS		9/32			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000023	PMID:22241092	PCS		1/6			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002162	PMID:36777704;PMID:25447906	PCS		3/5			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001629	PMID:23304577;PMID:31337854;PMID:30246735;PMID:20358602;PMID:22241092	PCS		3/42			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002714	PMID:21165303;PMID:31337854;PMID:36777704;PMID:30246735;PMID:32074972;PMID:38284454;PMID:22241092	PCS		34/42			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0002557	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000776	PMID:31337854;PMID:36777704;PMID:32074972;PMID:38284454	PCS		1/30			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001640	PMID:21165303;PMID:30246735;PMID:22241092;PMID:20358602	PCS		1/19			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0005565	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0005280	PMID:23304577;PMID:31337854;PMID:30246735;PMID:25447906;PMID:22241092;PMID:38284454	PCS		30/43			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0010066	PMID:38284454	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001636	PMID:31337854;PMID:30246735	PCS		1/24			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001511	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:30246735;PMID:22241092;PMID:38284454;PMID:20358602	PCS		39/52			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0200055	PMID:21165303;PMID:31337854;PMID:36777704;PMID:32074972;PMID:20358602;PMID:38284454;PMID:22241092	PCS		27/52			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000664	PMID:21165303;PMID:23304577;PMID:31337854;PMID:36777704;PMID:32074972;PMID:30246735;PMID:25447906;PMID:22241092;PMID:38284454	PCS		46/49			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001631	PMID:23304577;PMID:31337854	PCS		2/24			P	ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000388	OMIM:122470	IEA					P	HPO:skoehler[2018-10-08]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0001873	OMIM:122470	IEA					P	HPO:probinson[2009-02-17]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000028	PMID:23304577;PMID:31337854;PMID:32074972;PMID:38284454;PMID:20358602	PCS		15/25			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:122470	Cornelia de Lange syndrome 1		HP:0000545	PMID:31337854;PMID:22241092	PCS		5/26			P	HPO:probinson[2009-02-17];HPO:probinson[2024-11-23];ORCID:0000-0002-0736-9199[2024-11-23]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0002333	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0001311	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0000529	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0001250	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0002074	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0000007	OMIM:601780	IEA					I	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0000546	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0003208	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:601780	Ceroid lipofuscinosis, neuronal, 6		HP:0003205	OMIM:601780	IEA					P	HPO:iea[2009-02-17]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0002069	PMID:33473208	PCS		2/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0000252	PMID:33473208	PCS		2/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0001344	PMID:33473208	PCS		4/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0002266	PMID:33473208	PCS		1/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0001321	PMID:33473208	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0001263	PMID:33473208	PCS		8/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0001252	PMID:33473208	PCS		7/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0003593	PMID:33473208	PCS		7/8			C	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0012469	PMID:33473208	PCS		4/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0032792	PMID:33473208	PCS		1/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0002509	PMID:33473208	PCS		1/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0000007	PMID:33473208	PCS					I	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0020045	PMID:33473208	PCS		3/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0008897	PMID:33473208	PCS		3/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0000565	PMID:33473208	PCS		2/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0001249	PMID:33473208	PCS		8/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0000577	PMID:33473208	PCS		1/8			P	HPO:probinson[2022-10-03]
OMIM:620028	Developmental and epileptic encephalopathy 106		HP:0003623	PMID:33473208	PCS		1/8			C	HPO:probinson[2022-10-03]
OMIM:619871	Corneal dystrophy, punctiform and polychromatic pre-Descemet		HP:0003621	PMID:31782998	PCS					C	HPO:probinson[2022-06-25]
OMIM:619871	Corneal dystrophy, punctiform and polychromatic pre-Descemet		HP:0034327	PMID:31782998	PCS					P	HPO:probinson[2022-09-07]
OMIM:619871	Corneal dystrophy, punctiform and polychromatic pre-Descemet		HP:0000006	PMID:31782998	PCS					I	HPO:probinson[2022-06-25]
OMIM:603829	Ventricular fibrillation, familial, 1		HP:0001663	OMIM:603829	TAS					P	HPO:skoehler[2013-01-09]
OMIM:603829	Ventricular fibrillation, familial, 1		HP:0001649	PMID:4834245	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:603829	Ventricular fibrillation, familial, 1		HP:0001279	PMID:4834245	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0003676	OMIM:605280	IEA					C	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0002166	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0000012	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0003487	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0007340	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0000020	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0002064	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0002839	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0002061	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0001258	OMIM:605280	TAS					P	HPO:skoehler[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0000006	OMIM:605280	IEA					I	HPO:iea[2009-02-17]
OMIM:605280	Spastic paraplegia 13, autosomal dominant		HP:0001347	OMIM:605280	IEA					P	HPO:iea[2009-02-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0001919	PMID:17182750	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0001937	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0005575	PMID:17182750	PCS		9/12			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-03]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0001903	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0000790	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0000822	OMIM:612924	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0000093	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0100519	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0001873	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0003138	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0003259	OMIM:612924	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612924	Hemolytic uremic syndrome, atypical, susceptibility to, 4		HP:0000006	PMID:17182750	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0002575	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0001561	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000453	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0001762	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000463	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000452	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0004322	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0002032	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0003196	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000470	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0005280	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0012368	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03];HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0011461	PMID:31600779	PCS		2/2			C	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000316	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000921	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000007	PMID:31600779	PCS					I	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0008743	PMID:31600779	PCS		1/1			P	HPO:probinson[2022-06-03];HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0004209	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0003811	PMID:31600779	PCS		2/2			C	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0008689	PMID:31600779	PCS		1/1			P	HPO:probinson[2022-06-03];HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000248	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0000369	PMID:31600779	PCS		2/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0008439	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:619859	Phosphoribosylaminoimidazole carboxylase deficiency		HP:0004502	PMID:31600779	PCS		1/2			P	HPO:probinson[2022-06-03]
OMIM:617874	Polycystic liver disease 3 with or without kidney cysts		HP:0000107	PMID:28375157	PCS		4/5			P	HP:probinson[2019-04-19]
OMIM:617874	Polycystic liver disease 3 with or without kidney cysts		HP:0001407	PMID:28375157	PCS		5/5			P	HP:probinson[2019-04-19]
OMIM:617874	Polycystic liver disease 3 with or without kidney cysts		HP:0000006	PMID:28375157	PCS					I	HPO:skoehler[2019-04-18];HP:probinson[2019-04-19]
OMIM:171000	Peyronie disease		HP:0001475	OMIM:171000	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:171000	Peyronie disease		HP:0000924	OMIM:171000	IEA					P	HPO:iea[2009-02-17]
OMIM:171000	Peyronie disease		HP:0000119	OMIM:171000	IEA					P	HPO:iea[2009-02-17]
OMIM:171000	Peyronie disease		HP:0000006	OMIM:171000	TAS					I	HPO:probinson[2022-09-04]
OMIM:171000	Peyronie disease		HP:0005679	OMIM:171000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0001332	PMID:34636445	PCS					P	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0001288	PMID:34636445	PCS					P	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0007340	PMID:34636445	PCS					P	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0011463	PMID:34636445	PCS		18/40			C	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0003581	PMID:34636445	PCS		22/40			C	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0001258	PMID:34636445	PCS					P	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0012049	PMID:34636445	PCS					P	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0000006	PMID:34636445	PCS					I	HPO:probinson[2022-03-23]
OMIM:619681	Dystonia, early-onset, and/or spastic paraplegia		HP:0001347	PMID:34636445	PCS					P	HPO:probinson[2022-03-23]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0008936	PMID:24995870;OMIM:615905	PCS		17/17			P	HPO:probinson[2023-01-30];HPO:skoehler[2014-08-24]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0000252	OMIM:615905	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0000684	OMIM:615905	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0002133	PMID:24995870	PCS		5/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0001344	PMID:24995870	PCS		8/8			P	HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0001266	PMID:24995870	PCS		2/8			P	HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0001332	PMID:24995870	PCS		2/8			P	HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0001263	PMID:24995870	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0001251	OMIM:615905	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0012448	OMIM:615905	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0000705	OMIM:615905	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0000817	PMID:24995870	PCS		2/8			P	HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0031165	OMIM:615905	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0002509	PMID:24995870	PCS		5/7			P	HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0000668	OMIM:615905	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0000007	PMID:24995870	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0200134	PMID:24995870	PCS		8/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0001257	OMIM:615905	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0002500	OMIM:615905	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0004305	OMIM:615905	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615905	Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta		HP:0003623	PMID:24995870	PCS		8/8			C	HPO:probinson[2023-01-30]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002243	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0001596	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002024	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002164	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0001907	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0000518	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002917	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0001903	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0000217	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0000953	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0003745	OMIM:175500	IEA					I	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0001324	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002039	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002014	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0003401	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002573	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002672	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002013	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0004390	OMIM:175500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0100759	OMIM:175500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0000206	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0001217	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002900	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002901	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0008404	OMIM:175500	TAS					P	HPO:skoehler[2013-05-03]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0002027	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:175500	Polyposis, skin pigmentation, alopecia, and fingernail changes		HP:0004326	OMIM:175500	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0003554	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0002872	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0002015	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0003577	PMID:11172068;OMIM:254210	PCS		20/20			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0000486	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0002882	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0002098	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0003473	PMID:11172068	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0001283	PMID:11172068	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0002033	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0003397	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0030208	PMID:11172068	PCS		0/5			P	HPO:probinson[2022-09-02]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0000508	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0000007	PMID:11172068	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0002804	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0002747	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0000597	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0001612	OMIM:254210	IEA					P	HPO:iea[2009-02-17]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0003402	PMID:11172068	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0003403	OMIM:254210	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254210	Myasthenic syndrome, congenital, 6, presynaptic		HP:0003623	PMID:11172068	PCS					C	HPO:probinson[2022-09-02]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0002069	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0001252	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0012707	PMID:26002053	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0002020	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0012708	PMID:26002053	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0003593	PMID:37985816;PMID:26002053	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0032794	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0033725	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0001508	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0100704	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0002119	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0008897	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0002553	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0001562	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0002179	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0000252	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0025373	PMID:26002053	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0002376	PMID:37985816	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0001263	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0010851	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0011448	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0032792	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0000007	PMID:26002053	PCS					I	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0000648	PMID:37985816;PMID:26002053	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0000768	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:620772	Developmental and epileptic encephalopathy 113		HP:0001511	PMID:37985816;PMID:26002053	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-06]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002421	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0004840	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000321	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0004322	OMIM:259720	IEA					P	HPO:skoehler[2019-04-18]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001250	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0003593	PMID:16813530	PCS		3/3			C	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001290	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0011499	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000639	PMID:16813530	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0003826	OMIM:259720	TAS					C	HPO:skoehler[2010-06-20]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000238	OMIM:259720	TAS					P	HPO:probinson[2009-02-17]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0007204	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0004437	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0007965	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0003623	PMID:15108279;PMID:23772242	PCS		2/2			C	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000252	PMID:16813530;PMID:23772242	PCS		2/4			P	HPO:probinson[2022-07-01];HPO:skoehler[2019-02-22];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002510	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001541	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002197	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001141	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002904	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002509	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000007	PMID:12627228	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000648	PMID:16813530;PMID:23772242	PCS		2/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-07-01];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001978	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002901	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000520	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001974	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0003015	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001276	PMID:16813530;PMID:15108279;PMID:23772242	PCS		3/5			P	HPO:probinson[2022-07-01];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002169	PMID:16813530	PCS		1/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0010628	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001399	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000343	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0003256	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002240	PMID:15108279	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0011002	PMID:16813530;PMID:15108279;PMID:23772242	PCS		5/5			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01];HPO:probinson[2022-02-19];HPO:skoehler[2013-06-10];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001903	PMID:16813530	PCS		2/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0011001	PMID:15108279;PMID:23772242	PCS		2/2			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000737	PMID:23772242	PCS		1/1			P	HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0030043	PMID:16813530	PCS		1/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002878	OMIM:259720	IEA					P	HPO:skoehler[2019-04-18]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002119	PMID:16813530;PMID:23772242	PCS		2/4			P	HPO:probinson[2022-07-01];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000212	PMID:16813530	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001744	PMID:15108279	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001347	PMID:16813530;PMID:15108279	PCS		2/4			P	HPO:probinson[2022-07-01];HPO:skoehler[2019-02-22];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0008936	PMID:16813530;PMID:23772242	PCS		2/4			P	HPO:probinson[2022-07-01];HPO:skoehler[2019-02-22];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0002059	PMID:16813530;PMID:23772242	PCS		3/4			P	HPO:probinson[2022-07-01];HPO:skoehler[2019-02-22];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0030328	OMIM:259720	TAS					P	HPO:probinson[2015-04-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000505	PMID:15108279	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000543	PMID:16813530	PCS		2/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001510	PMID:16813530	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001433	PMID:16813530	PCS		2/3			P	HPO:probinson[2022-07-01]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001873	PMID:16813530;PMID:15108279	PCS		3/4			P	HPO:probinson[2022-07-01];HPO:skoehler[2019-02-22];HPO:probinson[2022-02-19]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0000347	OMIM:259720	IEA					P	HPO:skoehler[2019-02-22]
OMIM:259720	Osteopetrosis, autosomal recessive 5		HP:0001876	PMID:16813530	PCS		1/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-07-01]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0001265	OMIM:615911	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0000011	PMID:24934289	PCS		1/8			P	HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0002015	PMID:24934289	PCS		6/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0003676	PMID:24934289	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0001300	OMIM:615911	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0003596	PMID:24934289	PCS		5/7			C	HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0003487	PMID:24934289	PCS		6/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0002145	PMID:24934289	PCS		7/7			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0001283	PMID:24934289	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0002120	PMID:24934289	PCS		1/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0001260	PMID:24934289	PCS		8/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0003584	PMID:24934289	PCS		2/7			C	HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0001284	PMID:24934289	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0001251	PMID:24934289	PCS		5/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0100543	PMID:24934289	PCS		7/8			P	HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0000727	OMIM:615911	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0000407	PMID:24934289	PCS		2/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0000508	PMID:24934289	PCS		1/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0007354	PMID:24934289	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0003701	PMID:24934289	PCS		4/8			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-27]
OMIM:615911	Frontotemporal dementia and/or amyotrophic lateral sclerosis 2		HP:0000006	PMID:24934289	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:211980	Lung cancer, susceptibility to		HP:0030358	OMIM:211980	TAS					P	HPO:probinson[2020-07-15]
OMIM:211980	Lung cancer, susceptibility to		HP:0001442	OMIM:211980	TAS					I	HPO:skoehler[2019-02-22]
OMIM:211980	Lung cancer, susceptibility to		HP:0006519	OMIM:211980	TAS					P	HPO:iea[2009-02-17]
OMIM:211980	Lung cancer, susceptibility to		HP:0030078	OMIM:211980	TAS					P	HPO:probinson[2020-07-15]
OMIM:211980	Lung cancer, susceptibility to		HP:0000006	OMIM:211980	TAS					I	HPO:skoehler[2019-02-22]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0003577	PMID:22658544	PCS		6/6			C	HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0002650	PMID:22658544	PCS		4/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0002144	OMIM:612918	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0000089	PMID:22658544	PCS		2/6			P	HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0001442	PMID:22658544	PCS					I	HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0025104	PMID:22658544	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0004099	PMID:22658544	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0010301	OMIM:612918	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0012721	PMID:22658544	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0012032	PMID:22658544	PCS		6/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0100559	PMID:22658544	PCS		5/5			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0001548	OMIM:612918	TAS	HP:0003577				P	HPO:skoehler[2012-11-18]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0030680	OMIM:612918	TAS					P	HPO:skoehler[2012-11-18]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0001528	OMIM:612918	TAS		HP:0040280			P	HPO:skoehler[2012-11-18]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0001852	PMID:22658544	PCS		4/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0003745	OMIM:612918	TAS					I	HPO:skoehler[2015-12-30]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0002667	PMID:22658544	PCS		1/6			P	HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0000465	PMID:22658544	PCS		1/6			P	HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0004437	OMIM:612918	TAS					P	HPO:skoehler[2012-11-18]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0001744	PMID:22658544	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-01]
OMIM:612918	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi		HP:0000324	OMIM:612918	TAS					P	HPO:skoehler[2012-10-17]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0007549	OMIM:242300	TAS					P	HPO:probinson[2012-09-16]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0003577	PMID:9326318	IEA		17/17			C	HPO:probinson[2022-03-11]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0001036	OMIM:242300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0000232	OMIM:242300	TAS					P	HPO:skoehler[2013-01-21]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0001596	PMID:9326318	PCS		7/17			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0001371	OMIM:242300	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0002164	OMIM:242300	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0025092	OMIM:242300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0008070	OMIM:242300	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0008064	PMID:9326318	PCS		17/17			P	HPO:probinson[2022-03-11]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0007431	PMID:9326318	PCS	HP:0003577	7/17			P	HPO:probinson[2022-03-11]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0000007	PMID:7824952	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0000656	PMID:9326318	PCS		16/17			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0001019	OMIM:242300	TAS					P	HPO:skoehler[2013-01-21]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0008404	OMIM:242300	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0000972	PMID:9326318	PCS		16/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-11]
OMIM:242300	Ichthyosis, congenital, autosomal recessive 1		HP:0007479	PMID:9326318	PCS	HP:0003577	14/17			P	HPO:probinson[2022-03-11];HPO:probinson[2022-03-11]
OMIM:620014	Lymphatic malformation 12		HP:0031944	PMID:35235341	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0001561	PMID:35235341	PCS		2/5			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0025671	PMID:35235341	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0003577	PMID:35235341	PCS		2/7			C	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0000034	PMID:35235341	PCS		3/5			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0000023	PMID:35235341	PCS		2/5			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0025676	PMID:35235341	PCS		7/7			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0200117	PMID:35235341	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0001791	PMID:35235341	PCS		5/5			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0001790	PMID:35235341	PCS		5/7			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0011421	PMID:35235341	PCS		1/7			C	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0034197	PMID:35235341	PCS		2/7			C	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0034198	PMID:35235341	PCS		3/7			C	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0000007	PMID:35235341	PCS					I	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0025677	PMID:35235341	PCS		6/6			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0003811	PMID:35235341	PCS		1/7			C	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0001004	PMID:35235341	PCS		7/7			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0002643	PMID:35235341	PCS		4/7			P	HPO:probinson[2022-08-28]
OMIM:620014	Lymphatic malformation 12		HP:0000962	PMID:35235341	PCS		1/5			P	HPO:probinson[2022-08-28]
OMIM:131430	EOSINOPHILOPENIA		HP:0002960	PMID:6465701	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:131430	EOSINOPHILOPENIA		HP:0001025	PMID:6465701	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:131430	EOSINOPHILOPENIA		HP:0001871	OMIM:131430	IEA					P	HPO:iea[2009-02-17]
OMIM:131430	EOSINOPHILOPENIA		HP:0031891	PMID:6465701	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:131430	EOSINOPHILOPENIA		HP:0003193	PMID:6465701	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:619695	Rauch-Steindl syndrome		HP:0000286	PMID:29760529	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000582	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000343	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0004322	PMID:31171569	PCS		2/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0001252	PMID:29760529;PMID:29892088;PMID:30345613;PMID:31171569	PCS		7/7			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0002240	PMID:29760529	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0003593	PMID:29760529	IEA		1/1			C	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0001508	PMID:30345613;PMID:31171569	PCS		3/4			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000718	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0011220	PMID:31171569	PCS		1/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000739	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0012450	PMID:30345613;PMID:31171569	PCS		3/4			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0011461	PMID:29892088;PMID:30345613;PMID:31171569	PCS		6/6			C	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0004719	PMID:31171569	PCS		1/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000316	PMID:29760529;PMID:29892088;PMID:30345613	PCS		3/4			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000733	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0008897	PMID:31171569	PCS		2/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000752	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000411	PMID:29760529;PMID:30345613	PCS		2/2			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0006610	PMID:29760529	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0001249	PMID:29892088;PMID:31171569	PCS		4/4			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0002553	PMID:29892088;PMID:30345613	PCS		2/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000252	PMID:29760529;PMID:29892088;PMID:31171569	PCS		6/6			P	HPO:probinson[2022-03-01];HPO:probinson[2022-03-01];HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000233	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000431	PMID:29760529;PMID:29892088;PMID:30345613;PMID:31171569	PCS		5/7			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000331	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0005268	PMID:29760529	PCS		1/1			C	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0011968	PMID:29892088	PCS		2/2			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0009907	PMID:29760529	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0001263	PMID:29760529;PMID:30345613;PMID:31171569	PCS		5/5			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0005280	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0012584	PMID:31171569	PCS		1/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000506	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0001738	PMID:31171569	PCS		1/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000729	PMID:31171569	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000629	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000348	PMID:29760529	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0007874	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0004209	PMID:29760529	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0001511	PMID:29892088;PMID:30345613;PMID:31171569	PCS		6/6			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000960	PMID:30345613	PCS		1/1			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000322	PMID:29892088	PCS		2/2			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0009899	PMID:31171569	PCS		1/3			P	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000006	PMID:29760529	PCS					I	HPO:probinson[2022-03-01]
OMIM:619695	Rauch-Steindl syndrome		HP:0000347	PMID:29892088	PCS		2/2			P	HPO:probinson[2022-03-01]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003015	PMID:24387991	PCS		4/4			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0002982	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0007957	PMID:24387991	PCS		1/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0001132	PMID:24387991	PCS		1/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003016	PMID:24387990	PCS					P	HPO:probinson[2015-03-08]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0002980	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0008905	PMID:24387991	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0004565	OMIM:608940	TAS	HP:0011463				P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000486	PMID:24387991	PCS		2/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0001156	OMIM:608940	TAS					P	HPO:skoehler[2015-04-05]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0004322	PMID:24387991;PMID:24387990	PCS		10/10			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0009918	PMID:24387991	PCS		2/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003375	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003593	PMID:24387991	PCS		4/4			C	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0010049	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0009381	OMIM:608940	TAS					P	HPO:probinson[2015-02-22]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000639	PMID:24387991	PCS		2/4			P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0002979	PMID:24387991	PCS		4/4			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0007663	PMID:24387991;PMID:24387990	PCS		8/10			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0002812	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0008897	OMIM:608940	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0007401	PMID:24387991	PCS		1/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0002657	PMID:24387991	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0001105	PMID:24387991	PCS		2/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003026	PMID:24387991	PCS		4/4			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000550	PMID:24387991	PCS		1/1			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0002650	PMID:24387991	PCS		1/4			P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0001387	PMID:24387990	PCS					P	HPO:probinson[2015-03-08]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003025	PMID:24387990	PCS		8/8			P	HPO:probinson[2015-03-08];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003300	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0003021	PMID:24387990	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0030329	PMID:24387991	PCS		1/1			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000529	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0031141	PMID:24387991	PCS		2/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0008002	PMID:24387990	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000926	PMID:24387991;PMID:24387990	PCS		12/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-16];HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0001999	PMID:24387991	PCS		0/4			P	HPO:probinson[2015-02-22];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000007	PMID:24387990	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000887	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000689	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000568	PMID:24387991	PCS		2/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000403	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000548	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0008821	OMIM:608940	TAS					P	HPO:probinson[2009-02-17]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000545	PMID:24387991	PCS		2/4			P	HPO:probinson[2024-03-16]
OMIM:608940	Spondylometaphyseal dysplasia with cone-rod dystrophy		HP:0000588	PMID:24387991	PCS		1/4			P	HPO:probinson[2024-03-16]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0000486	PMID:15671264	IEA		4/11			P	HPO:probinson[2010-08-17]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0000529	PMID:15671264	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-05]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0001131	PMID:15671264	PCS	HP:0003623	11/11			P	HPO:probinson[2022-09-05]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0007709	PMID:15671264	PCS		1/4			P	HPO:probinson[2022-09-05]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0000613	PMID:15671264	PCS		0/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-05]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0011487	PMID:15671264	PCS					P	HPO:skoehler[2014-05-04];HPO:probinson[2022-09-05]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0000006	PMID:15671264	PCS					I	HPO:probinson[2012-07-22]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0000501	PMID:15671264	IEA		3/11			P	HPO:probinson[2012-07-22]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0200020	PMID:15671264	PCS		0/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-05]
OMIM:610048	Corneal dystrophy, congenital stromal		HP:0003623	PMID:15671264	PCS		11/11			C	HPO:probinson[2022-09-05]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003577	PMID:30215711	PCS		2/2			C	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0001371	OMIM:618414	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0001252	PMID:30215711	PCS		2/2			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003273	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0001270	OMIM:618414	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0030319	PMID:30215711	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0100297	PMID:30215711	PCS		2/2			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0040081	PMID:30215711	PCS		0/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0002878	PMID:30215711	PCS		2/2			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003803	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0000218	PMID:30215711	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003701	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0001522	PMID:30215711	PCS		1/2			C	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003327	PMID:30215711	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003403	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0002058	PMID:30215711	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0001561	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003324	PMID:30215711	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0011968	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0001284	PMID:30215711	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0032988	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0006380	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0040288	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0001558	PMID:30215711	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0000007	PMID:30215711	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0002747	PMID:30215711	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0002987	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0002104	PMID:30215711	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0000467	PMID:30215711	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:618414	Myopathy, congenital, with fast-twitch (type II) fiber atrophy		HP:0003557	PMID:30215711	PCS		2/2			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0002366	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0001265	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0002300	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0003202	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0002015	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0003676	OMIM:616439	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0002463	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0002145	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0001283	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0002120	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0001260	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0003581	PMID:25803835	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-03]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0002380	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0007354	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0000734	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0000741	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0001324	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0000751	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0000006	PMID:25803835	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-03]
OMIM:616439	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4		HP:0001347	OMIM:616439	TAS					P	HPO:skoehler[2015-07-26]
OMIM:112410	Hypertension and brachydactyly syndrome		HP:0005863	PMID:25961942	PCS		46/47			P	HPO:probinson[2023-02-19]
OMIM:112410	Hypertension and brachydactyly syndrome		HP:0004322	PMID:25961942	PCS		47/47			P	HPO:skoehler[2015-07-26]
OMIM:112410	Hypertension and brachydactyly syndrome		HP:0000822	PMID:25961942	PCS		47/47			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:112410	Hypertension and brachydactyly syndrome		HP:0010049	PMID:25961942	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:112410	Hypertension and brachydactyly syndrome		HP:0000006	PMID:25961942	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:112410	Hypertension and brachydactyly syndrome		HP:0009803	PMID:25961942	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:112410	Hypertension and brachydactyly syndrome		HP:0010579	PMID:25961942	PCS		HP:0040283			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-19]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0003577	PMID:19461874	PCS		4/4			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-27]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0000486	PMID:19461874	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-27]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0001260	PMID:19461874	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-27]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0001251	PMID:19461874	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-27]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0001350	PMID:19461874	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-27]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0000007	PMID:19461874	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-27]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0009878	PMID:19461874	PCS		4/4			P	HPO:probinson[2023-01-27]
OMIM:613227	Spinocerebellar ataxia, autosomal recessive 34		HP:0001337	PMID:19461874	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-01-27]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003554	PMID:9758617	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003577	PMID:9689136	PCS		6/6			C	HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003198	OMIM:603034	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003473	PMID:9758617;PMID:9689136	PCS		12/12			P	HPO:probinson[2012-04-12];HPO:probinson[2023-04-02];HPO:probinson[2023-04-02];HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003199	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0001252	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003593	OMIM:603034	TAS					C	HPO:probinson[2012-04-12]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0001290	OMIM:603034	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003690	PMID:9758617	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0008872	OMIM:603034	TAS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2012-04-12]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003307	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003803	PMID:9758617	PCS		2/2			P	HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0000597	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003403	PMID:9689136	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003621	PMID:9758617	PCS		6/6			C	HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003324	PMID:9758617	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0002015	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0002650	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003388	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003443	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0001260	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0002093	OMIM:603034	TAS					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0030208	PMID:9758617;PMID:9689136	PCS		0/12			P	HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0000508	PMID:9758617	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0000007	PMID:9689136	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0002747	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0001612	OMIM:603034	IEA					P	HPO:iea[2009-02-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0003436	OMIM:603034	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603034	Myasthenic syndrome, congenital, 5		HP:0000467	PMID:9758617	PCS		1/6			P	HPO:probinson[2023-04-02]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000486	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0004322	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001250	PMID:21187176	PCS		1/7			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001252	OMIM:615656	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0003593	PMID:21187176	PCS		2/7			C	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001251	OMIM:615656	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001290	OMIM:615656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000280	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0031987	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0009381	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0033051	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0006150	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000319	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0011463	PMID:21187176	PCS		5/7			C	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0003829	OMIM:615656	TAS					I	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000954	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000316	PMID:21187176	PCS		1/7			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001249	PMID:21187176	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0002312	OMIM:615656	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000175	OMIM:615656	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0002354	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0011968	OMIM:615656	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001263	PMID:21187176	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0034392	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000729	PMID:21187176	PCS		1/7			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000722	OMIM:615656	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000601	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000400	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0034391	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000006	PMID:21187176	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000460	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000581	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001270	PMID:21187176	PCS		3/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0040082	OMIM:615656	TAS					P	HPO:skoehler[2014-11-27]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0040079	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000739	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000733	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000414	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000337	OMIM:615656	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001627	OMIM:615656	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0030084	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001166	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000274	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000750	PMID:21187176	PCS		4/7			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000276	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0002099	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0005681	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000709	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0012760	PMID:21187176	PCS		3/7			P	HPO:probinson[2022-12-11]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001357	OMIM:615656	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0007018	OMIM:615656	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0001238	OMIM:615656	TAS					P	HPO:skoehler[2014-05-09]
OMIM:615656	Chromosome 15q11.2 deletion syndrome		HP:0000347	PMID:21187176	PCS		1/7			P	HPO:probinson[2022-12-11]
OMIM:275355	Squamous cell carcinoma, head and neck		HP:0002860	OMIM:275355	TAS					P	HPO:skoehler[2009-02-17]
OMIM:275355	Squamous cell carcinoma, head and neck		HP:0000007	OMIM:275355	TAS					I	HPO:skoehler[2009-02-17]
OMIM:617041	Duane retraction syndrome 3 with or without deafness		HP:0000365	PMID:27181683	PCS		3/14			P	HPO:probinson[2022-09-26]
OMIM:617041	Duane retraction syndrome 3 with or without deafness		HP:0000661	PMID:27181683	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617041	Duane retraction syndrome 3 with or without deafness		HP:0000634	PMID:27181683	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617041	Duane retraction syndrome 3 with or without deafness		HP:0000542	PMID:27181683	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617041	Duane retraction syndrome 3 with or without deafness		HP:0009921	PMID:27181683	PCS					P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:617041	Duane retraction syndrome 3 with or without deafness		HP:0000006	PMID:27181683	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:233300	Ovarian dysgenesis 1		HP:0000939	OMIM:233300	IEA					P	HPO:iea[2009-02-17]
OMIM:233300	Ovarian dysgenesis 1		HP:0003621	PMID:7553856	PCS					C	HPO:probinson[2022-06-11]
OMIM:233300	Ovarian dysgenesis 1		HP:0000133	OMIM:233300	IEA					P	HPO:iea[2009-02-17]
OMIM:233300	Ovarian dysgenesis 1		HP:0000837	OMIM:233300	IEA					P	HPO:iea[2009-02-17]
OMIM:233300	Ovarian dysgenesis 1		HP:0000007	PMID:7553856	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-11]
OMIM:233300	Ovarian dysgenesis 1		HP:0000786	OMIM:233300	IEA					P	HPO:iea[2009-02-17]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0001891	PMID:18451993	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0003540	PMID:18451993	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0004791	PMID:23268370	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0002592	PMID:18451993	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0032244	PMID:18451993	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0000007	PMID:25102815	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2020-03-28]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0030361	PMID:18451993	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0032575	PMID:25102815	PCS					P	HPO:probinson[2020-03-14]
OMIM:618372	Gastrointestinal ulceration, recurrent, with dysfunctional platelets		HP:0002588	PMID:25102815	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0000551	PMID:8485576	PCS		0/1			P	HPO:skoehler[2015-01-20];HPO:probinson[2022-12-04]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0011506	OMIM:608161	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0012508	PMID:8485576	PCS		1/1			P	HPO:skoehler[2015-01-20];HPO:probinson[2022-12-04]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0000613	OMIM:608161	TAS					P	HPO:skoehler[2015-01-20]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0007663	PMID:8485576	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-04]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0000505	PMID:8485576	PCS	HP:0003581	1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2022-12-04]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0011510	OMIM:608161	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0007401	OMIM:608161	TAS					P	HPO:skoehler[2015-07-26]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0025710	PMID:8485576	PCS		1/1			C	HPO:probinson[2022-12-04]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0007677	PMID:8485576	PCS		1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2022-12-04]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0007754	OMIM:608161	IEA					P	HPO:skoehler[2015-01-27]
OMIM:608161	Macular dystrophy, vitelliform, 3		HP:0000006	PMID:8485576	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-12-04]
OMIM:617055	PERCHING syndrome		HP:0002015	PMID:27392078	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0002650	PMID:27392078	PCS		0/4			P	HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0011968	PMID:27392078	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0000293	PMID:27392078	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0002098	OMIM:617055	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617055	PERCHING syndrome		HP:0025278	PMID:27392078	PCS		1/5			P	HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0003593	PMID:27392078	PCS		5/5			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0005280	PMID:27392078	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0012385	PMID:27392078	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0034392	PMID:27392078	PCS		3/4			P	HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0000007	PMID:27392078	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0001945	PMID:27392078	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0000218	PMID:27392078	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0000510	PMID:27392078	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0000961	PMID:27392078	PCS		1/5			P	HPO:probinson[2023-02-08]
OMIM:617055	PERCHING syndrome		HP:0001249	PMID:27392078	PCS		1/3			P	HPO:probinson[2023-02-08]
OMIM:184300	Spondylosis, cervical		HP:0008480	OMIM:184300	IEA					P	HPO:iea[2009-02-17]
OMIM:184300	Spondylosis, cervical		HP:0003302	OMIM:184300	IEA					P	HPO:iea[2009-02-17]
OMIM:184300	Spondylosis, cervical		HP:0003298	OMIM:184300	IEA					P	HPO:iea[2009-02-17]
OMIM:184300	Spondylosis, cervical		HP:0002758	OMIM:184300	IEA					P	HPO:iea[2009-02-17]
OMIM:184300	Spondylosis, cervical		HP:0000006	OMIM:184300	IEA					I	HPO:iea[2009-02-17]
OMIM:184300	Spondylosis, cervical		HP:0003304	OMIM:184300	IEA					P	HPO:iea[2009-02-17]
OMIM:608175	Autoimmune thyroid disease, susceptibility to, 3		HP:0100646	OMIM:608175	IEA					P	HPO:probinson[2013-02-23]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000121	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000486	PMID:35344616	PCS		4/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000365	PMID:35344616	PCS		3/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0004322	PMID:35344616	PCS	HP:0003593	22/22			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001052	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0003196	PMID:35344616	PCS		22/22			P	HPO:probinson[2013-04-09];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0005011	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0010292	OMIM:268310	IEA					P	HPO:skoehler[2010-06-18]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0010055	PMID:35344616	PCS		8/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0010297	PMID:35344616	PCS		17/22			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002937	PMID:35344616;PMID:15952209	PCS		21/24			P	HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0009466	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000637	PMID:35344616	PCS		15/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0005648	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000358	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000995	PMID:35344616	PCS		4/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000494	PMID:35344616	PCS		7/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0011927	OMIM:268310	TAS					P	HPO:probinson[2013-12-18];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0011800	PMID:35344616	PCS		21/22			P	HPO:skoehler[2013-11-28]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0003083	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0009177	PMID:15952209	PCS		2/2			P	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002948	OMIM:268310	TAS					P	HPO:skoehler[2013-06-23]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002827	PMID:35344616	PCS		3/19			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000767	PMID:35344616	PCS		10/21			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000921	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000007	PMID:10932186	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002944	OMIM:268310	TAS					P	HPO:skoehler[2013-06-23]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000527	PMID:35344616	PCS		16/22			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000520	PMID:35344616	PCS		14/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000369	PMID:35344616	PCS		14/21			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000126	PMID:15952209	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001853	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000582	PMID:35344616	PCS		11/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001792	PMID:15952209	PCS		2/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0003577	PMID:15952209	PCS		2/2			C	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000189	PMID:35344616	PCS		7/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000343	PMID:35344616	PCS		11/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001156	PMID:35344616;PMID:15952209	PCS		24/24			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000463	OMIM:268310;PMID:35344616	PCS		22/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000064	PMID:35344616	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000060	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001705	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000219	PMID:35344616	PCS		13/22			P	HPO:skoehler[2013-06-04]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0030084	PMID:35344616	PCS		17/21			P	HPO:skoehler[2014-09-21]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000059	PMID:35344616	PCS		2/11			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000212	PMID:35344616	PCS		17/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000696	OMIM:268310	TAS					P	HPO:skoehler[2013-06-23]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0006216	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0004279	PMID:35344616	PCS		19/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002650	PMID:35344616;PMID:15952209	PCS		16/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000075	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000470	PMID:35344616	PCS		14/22			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000902	PMID:35344616;PMID:15952209	PCS		20/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001837	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000508	PMID:35344616	PCS		3/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0008467	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0005914	OMIM:268310	TAS					P	HPO:skoehler[2013-06-23]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001159	PMID:35344616	PCS		6/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002007	PMID:15952209	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000347	PMID:35344616	PCS		15/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000286	PMID:35344616	PCS		7/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0010804	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0006394	PMID:35344616	PCS		13/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0011220	PMID:35344616;PMID:15952209	PCS		23/24			P	HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000954	PMID:35344616	PCS		5/19			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000316	PMID:35344616;PMID:15952209	PCS		23/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000678	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000158	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000278	PMID:35344616	PCS		15/22			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001249	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0009804	PMID:35344616	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000054	PMID:35344616;PMID:15952209	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002750	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001382	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000171	PMID:35344616	PCS		6/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001263	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0012385	PMID:35344616	PCS		4/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001537	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000207	PMID:35344616;PMID:15952209	PCS		17/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002986	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000202	PMID:35344616	PCS		5/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000322	PMID:35344616	PCS		6/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000960	PMID:35344616	PCS		1/19			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000047	PMID:35344616	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002984	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000023	PMID:35344616	PCS		3/19			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000260	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002164	PMID:35344616	PCS		8/21			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0004220	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0012368	OMIM:268310	TAS					P	HPO:skoehler[2014-11-27]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0009883	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0009882	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0008551	PMID:35344616	PCS		2/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0001627	PMID:35344616	PCS		4/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0002714	PMID:35344616	PCS		17/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000256	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000154	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0003027	PMID:35344616	PCS		22/22			P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000431	PMID:35344616	PCS		21/22			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-21]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000270	OMIM:268310	TAS					P	HPO:skoehler[2013-06-23]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000272	OMIM:268310	IEA					P	HPO:iea[2009-02-17]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0004590	OMIM:268310	TAS					P	HPO:skoehler[2013-06-23]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0005280	PMID:35344616	PCS		15/22			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0011304	PMID:35344616;PMID:15952209	PCS		14/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0200055	OMIM:268310	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000787	PMID:15952209	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:268310	Robinow syndrome, autosomal recessive		HP:0000028	PMID:35344616	PCS		5/10			P	HPO:iea[2009-02-17]
OMIM:104500	Amelogenesis imperfecta, type IB		HP:0000705	OMIM:104500	IEA					P	HPO:iea[2009-02-17]
OMIM:104500	Amelogenesis imperfecta, type IB		HP:0000006	OMIM:104500	IEA					I	HPO:iea[2009-02-17]
DECIPHER:58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0003067	DECIPHER:58	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0006394	DECIPHER:58	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0008873	DECIPHER:58	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0002986	DECIPHER:58	IEA					P	HPO:skoehler[2013-05-29]
OMIM:180600	Ringed hair		HP:0001595	OMIM:180600	IEA					P	HPO:iea[2009-02-17]
OMIM:180600	Ringed hair		HP:0000006	OMIM:180600	IEA					I	HPO:iea[2009-02-17]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0003477	PMID:30298599	PCS		10/11			P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0001397	PMID:30298599	PCS		4/11			P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0003444	PMID:30298599	IEA					P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0001265	OMIM:618400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0003621	OMIM:618400	IEA					C	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0003676	OMIM:618400	IEA					C	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0001178	PMID:30298599	PCS					P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0001288	OMIM:618400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0001761	OMIM:618400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0003693	PMID:30298599	PCS					P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0006937	PMID:30298599	IEA					P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0002460	PMID:30298599	PCS	HP:0011462				P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0001284	OMIM:618400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0002490	OMIM:618400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0008180	PMID:30298599	PCS					P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0007230	PMID:30298599	PCS					P	HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0009027	OMIM:618400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0000007	PMID:30298599	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0002910	OMIM:618400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618400	Charcot-Marie-Tooth disease, axonal, type 2EE		HP:0001765	OMIM:618400	IEA					P	HPO:skoehler[2019-09-07]
OMIM:149400	Hyperekplexia 1		HP:0001276	OMIM:149400	IEA					P	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0002267	OMIM:149400	IEA					P	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0002375	OMIM:149400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:149400	Hyperekplexia 1		HP:0000023	OMIM:149400	IEA					P	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0001250	OMIM:149400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:149400	Hyperekplexia 1		HP:0003593	OMIM:149400	IEA					C	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0031951	OMIM:149400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:149400	Hyperekplexia 1		HP:0002827	OMIM:149400	IEA					P	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0001537	OMIM:149400	IEA					P	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0000007	OMIM:149400	IEA					I	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0002835	OMIM:149400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:149400	Hyperekplexia 1		HP:0002359	OMIM:149400	IEA					P	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0000006	OMIM:149400	IEA					I	HPO:iea[2009-02-17]
OMIM:149400	Hyperekplexia 1		HP:0002104	OMIM:149400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:149400	Hyperekplexia 1		HP:0001336	OMIM:149400	IEA					P	HPO:iea[2009-02-17]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002069	PMID:26576034;PMID:23615299	PCS		3/8			P	HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0010804	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000486	PMID:23615299	PCS		7/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26];HPO:probinson[2022-03-09]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0025268	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001252	PMID:26576034	PCS	HP:0003593	1/1			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001252	PMID:23615299	PCS		3/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001252	PMID:25900396	PCS		2/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0003196	PMID:23615299	PCS		2/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001251	OMIM:300912	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002020	PMID:25900396;PMID:23615299	PCS		4/9			P	HPO:probinson[2021-09-26];HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0003593	PMID:26576034;PMID:23615299	PCS		8/8			C	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002061	PMID:23615299	PCS		3/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0012469	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000718	PMID:26576034;PMID:23615299	PCS		3/8			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000954	PMID:26576034	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0008897	PMID:25900396;PMID:23615299	PCS		6/9			P	HPO:probinson[2021-09-26];HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0025336	PMID:25900396;PMID:23615299	PCS		3/9			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000752	PMID:26576034;PMID:23615299	PCS		5/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000311	PMID:23615299	PCS		3/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001249	PMID:23615299	PCS		7/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26];HPO:probinson[2022-03-09]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0003763	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0010519	PMID:26576034	PCS	HP:0011461	1/1			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0025650	PMID:25900396	PCS		1/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000494	PMID:25900396	PCS		2/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001344	PMID:26576034	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0011968	PMID:25900396	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001263	PMID:25900396;PMID:23615299	PCS		9/9			P	HPO:probinson[2021-09-26];HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0011927	PMID:26576034	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0100023	PMID:25900396	PCS		1/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000729	PMID:25900396	PCS		1/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0100739	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0004209	PMID:26576034	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002307	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000565	PMID:23615299	PCS		1/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000400	PMID:25900396	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000322	PMID:23615299	PCS		1/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000341	PMID:25900396;PMID:26576034;PMID:23615299	PCS		5/10			P	HPO:probinson[2021-09-26];HPO:skoehler[2018-10-08];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002521	PMID:23615299	PCS		2/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000463	OMIM:300912	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002123	OMIM:300912	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0025401	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002121	PMID:26576034;PMID:23615299	PCS		2/8			P	HPO:probinson[2021-09-26];HPO:skoehler[2018-10-08];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000020	PMID:26576034	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0012169	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001508	PMID:25900396	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0012172	PMID:23615299	PCS		2/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000817	PMID:23615299	PCS		3/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000739	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000733	PMID:26576034;PMID:23615299	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002714	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0012171	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0001423	PMID:26576034	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0008936	PMID:23615299	PCS		1/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000750	PMID:25900396;PMID:23615299	PCS		9/9			P	HPO:probinson[2021-09-26];HPO:probinson[2022-03-09];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0003189	PMID:25900396	PCS		2/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002133	OMIM:300912	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000233	PMID:25900396	PCS		2/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000430	PMID:25900396	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000194	PMID:25900396	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0010819	PMID:26576034;PMID:23615299	PCS		2/8			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0002572	PMID:25900396	PCS		1/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0005484	OMIM:300912;PMID:23615299	PCS		11/17			P	HPO:probinson[2021-09-26];HPO:skoehler[2015-12-30]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0005280	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0011787	PMID:25900396	PCS		1/2			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0012760	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0032792	PMID:26576034	PCS		1/1			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0007210	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000426	PMID:26576034	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-26]
OMIM:300912	Intellectual developmental disorder, X-linked 98		HP:0000303	PMID:23615299	PCS		1/7			P	HPO:probinson[2021-09-26]
OMIM:156520	Metatarsus varus, type I		HP:0001840	OMIM:156520	IEA					P	HPO:iea[2009-02-17]
OMIM:156520	Metatarsus varus, type I		HP:0000006	OMIM:156520	TAS					I	HPO:skoehler[2013-05-29]
OMIM:614212	Encephalopathy, acute, infection-induced, susceptibility to, 4		HP:0001298	OMIM:614212	IEA					P	HPO:skoehler[2015-01-27]
OMIM:614212	Encephalopathy, acute, infection-induced, susceptibility to, 4		HP:0001250	OMIM:614212	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614212	Encephalopathy, acute, infection-induced, susceptibility to, 4		HP:0000007	OMIM:614212	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614212	Encephalopathy, acute, infection-induced, susceptibility to, 4		HP:0002181	OMIM:614212	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614212	Encephalopathy, acute, infection-induced, susceptibility to, 4		HP:0001945	OMIM:614212	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614212	Encephalopathy, acute, infection-induced, susceptibility to, 4		HP:0000006	OMIM:614212	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614212	Encephalopathy, acute, infection-induced, susceptibility to, 4		HP:0001259	OMIM:614212	TAS					P	HPO:skoehler[2012-10-17]
OMIM:153470	Macrocephaly, benign familial		HP:0000343	OMIM:153470	IEA					P	HPO:iea[2009-02-17]
OMIM:153470	Macrocephaly, benign familial		HP:0004422	OMIM:153470	IEA					P	HPO:iea[2009-02-17]
OMIM:153470	Macrocephaly, benign familial		HP:0001475	OMIM:153470	IEA					I	HPO:iea[2009-02-17]
OMIM:153470	Macrocephaly, benign familial		HP:0002119	OMIM:153470	IEA					P	HPO:iea[2009-02-17]
OMIM:153470	Macrocephaly, benign familial		HP:0000268	OMIM:153470	IEA					P	HPO:iea[2009-02-17]
OMIM:153470	Macrocephaly, benign familial		HP:0002007	OMIM:153470	IEA					P	HPO:iea[2009-02-17]
OMIM:153470	Macrocephaly, benign familial		HP:0000256	OMIM:153470	IEA					P	HPO:iea[2009-02-17]
OMIM:153470	Macrocephaly, benign familial		HP:0000006	OMIM:153470	TAS					I	HPO:probinson[2022-09-04]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0000252	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0000494	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0000271	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0100490	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0000506	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0000508	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0008872	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0007766	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0001249	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:70	2p15-16.1 microdeletion syndrome		HP:0000126	DECIPHER:70	IEA					P	HPO:skoehler[2013-05-29]
OMIM:607508	Migraine with or without aura, susceptibility to, 5		HP:0002013	OMIM:607508	IEA					P	HPO:iea[2009-02-17]
OMIM:607508	Migraine with or without aura, susceptibility to, 5		HP:0002077	OMIM:607508	IEA					P	HPO:iea[2009-02-17]
OMIM:607508	Migraine with or without aura, susceptibility to, 5		HP:0000613	OMIM:607508	IEA					P	HPO:iea[2009-02-17]
OMIM:607508	Migraine with or without aura, susceptibility to, 5		HP:0002083	OMIM:607508	IEA					P	HPO:iea[2009-02-17]
OMIM:607508	Migraine with or without aura, susceptibility to, 5		HP:0002183	OMIM:607508	IEA					P	HPO:iea[2009-02-17]
OMIM:607508	Migraine with or without aura, susceptibility to, 5		HP:0002018	OMIM:607508	IEA					P	HPO:iea[2009-02-17]
OMIM:607508	Migraine with or without aura, susceptibility to, 5		HP:0000006	OMIM:607508	IEA					I	HPO:iea[2009-02-17]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0003577	PMID:33811546	PCS		19/19			C	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000365	PMID:33811546	PCS		3/19			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000684	PMID:33811546	PCS		3/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000260	PMID:33811546	PCS		10/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0003196	PMID:33811546	PCS		15/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000316	PMID:33811546	PCS		19/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000219	PMID:33811546	PCS		16/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000636	PMID:33811546	PCS		2/19			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000218	PMID:33811546	PCS		12/19			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000455	PMID:33811546	PCS		18/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0001249	PMID:33811546	PCS		7/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000175	PMID:33811546	PCS		1/19			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000574	PMID:33811546	PCS		17/19			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000232	PMID:33811546	PCS		7/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000691	PMID:33811546	PCS		3/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0001263	PMID:33811546	PCS		7/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0011823	PMID:33811546	PCS		16/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0005280	PMID:33811546	PCS		13/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000729	PMID:33811546	PCS		2/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000508	PMID:33811546	PCS		5/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0004209	PMID:33811546	PCS		3/18			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0001159	PMID:33811546	PCS		0/18			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000520	PMID:33811546	PCS		5/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000047	PMID:33811546	PCS		4/8			P	HPO:probinson[2022-05-13]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0007018	PMID:33811546	PCS		2/19			P	HPO:probinson[2022-04-24]
OMIM:619736	Teebi hypertelorism syndrome 2		HP:0000006	PMID:33811546	PCS					I	HPO:probinson[2022-04-24]
OMIM:606170	Genitopatellar syndrome		HP:0002025	PMID:22265014	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0001374	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0002023	PMID:22265014	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000684	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000365	PMID:22265014	PCS		3/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000046	PMID:22265014	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0003273	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001252	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001290	OMIM:606170	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606170	Genitopatellar syndrome		HP:0000280	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0033725	PMID:22265014	PCS		15/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0007165	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001601	PMID:22265014	PCS		6/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0002974	OMIM:606170	TAS		HP:0040284			P	HPO:skoehler[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000494	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000252	PMID:22265014	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000054	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0011968	PMID:22265014	PCS		6/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0001263	PMID:22265014	PCS		16/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0006380	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0008683	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000448	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000003	OMIM:606170	IEA		6/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000006	PMID:22265014	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000126	PMID:22265014	PCS		16/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000445	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000066	PMID:22265014	PCS		6/6			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0002089	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001156	OMIM:606170	TAS					P	HPO:skoehler[2014-11-26]
OMIM:606170	Genitopatellar syndrome		HP:0001274	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0003175	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001629	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0002999	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001302	PMID:22265014	PCS		3/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0009803	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001545	PMID:22265014	PCS		3/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0002015	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0001561	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0002650	PMID:22265014	PCS		5/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0001762	PMID:22265014	PCS		18/19			P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000431	PMID:22265014	PCS		9/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0030048	PMID:22265014	PCS		4/19			P	HPO:skoehler[2014-09-21];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0004794	PMID:22265014	PCS		2/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000426	PMID:22265014	PCS		5/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0002209	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000821	PMID:22265014	PCS		3/19			P	HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0006443	PMID:22265014	PCS		18/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0008665	PMID:22265014	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0001631	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0000028	PMID:22265014	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:606170	Genitopatellar syndrome		HP:0000347	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:606170	Genitopatellar syndrome		HP:0008823	OMIM:606170	IEA					P	HPO:iea[2009-02-17]
OMIM:600501	ABCD syndrome		HP:0001022	PMID:7778600	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-11]
OMIM:600501	Abcd syndrome		HP:0003577	PMID:7778600	PCS		1/1			C	HPO:probinson[2022-06-11]
OMIM:600501	ABCD syndrome		HP:0001520	PMID:7778600	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:600501	ABCD syndrome		HP:0000365	PMID:7778600	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-06-11]
OMIM:600501	ABCD syndrome		HP:0006958	PMID:7778600	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-11]
OMIM:600501	ABCD syndrome		HP:0002251	PMID:7778600	PCS		1/1			P	HPO:skoehler[2013-12-09];HPO:probinson[2022-06-11]
OMIM:600501	ABCD syndrome		HP:0005241	PMID:7778600	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:600501	ABCD syndrome		HP:0007894	OMIM:600501	TAS					P	HPO:probinson[2009-02-17]
OMIM:600501	ABCD syndrome		HP:0000007	PMID:7778600	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-06-11]
OMIM:600501	ABCD syndrome		HP:0001901	PMID:7778600	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:600501	Abcd syndrome		HP:0002227	PMID:7778600	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:600501	Abcd syndrome		HP:0003811	PMID:7778600	PCS		1/1			C	HPO:probinson[2022-06-11]
OMIM:600501	Abcd syndrome		HP:0002226	PMID:7778600	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:148050	KBG syndrome		HP:0001572	PMID:21782149	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0010804	PMID:21782149	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000343	PMID:21782149	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000463	PMID:21782149	PCS		7/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0004322	PMID:21782149	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0001250	OMIM:148050	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:148050	KBG syndrome		HP:0002162	PMID:21782149	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0012725	PMID:21782149	PCS		2/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0009464	PMID:21782149	PCS		2/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000316	PMID:21782149	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000954	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0009466	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0000637	PMID:21782149	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0001566	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0000411	PMID:21782149	PCS		6/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000311	OMIM:148050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148050	KBG syndrome		HP:0001249	PMID:21782149	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000677	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0000358	PMID:21782149	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000039	PMID:21782149	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0008438	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0000891	PMID:21782149	PCS		3/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000252	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0000494	PMID:21782149	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000574	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0004279	PMID:21782149	PCS		7/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0002750	PMID:21782149	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000430	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0001263	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0000294	PMID:21782149	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000470	PMID:21782149	PCS		2/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000902	OMIM:148050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148050	KBG syndrome		HP:0000506	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0002948	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0000508	PMID:21782149	PCS		6/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000426	PMID:21782149	PCS		5/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000307	PMID:21782149	PCS		2/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0004209	PMID:21782149	PCS		7/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000400	PMID:21782149	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0001159	OMIM:148050	IEA					P	HPO:iea[2009-02-17]
OMIM:148050	KBG syndrome		HP:0002942	PMID:21782149	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000664	PMID:21782149	PCS		5/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000465	PMID:21782149	PCS		2/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0007018	PMID:21782149	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000006	PMID:21782149	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000028	PMID:21782149	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000325	PMID:21782149	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:148050	KBG syndrome		HP:0000248	PMID:21782149	PCS		4/7			P	HPO:probinson[2022-09-25]
OMIM:157170	Holoprosencephaly 2		HP:0006988	PMID:10369266	PCS		2/4			P	HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0003577	PMID:10369266	PCS		4/4			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0009914	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0010626	OMIM:157170	TAS					P	HPO:probinson[2013-03-22]
OMIM:157170	Holoprosencephaly 2		HP:0001750	OMIM:157170	IEA					P	HPO:skoehler[2018-10-08]
OMIM:157170	Holoprosencephaly 2		HP:0001250	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0000161	OMIM:157170	TAS					P	HPO:probinson[2024-03-29]
OMIM:157170	Holoprosencephaly 2		HP:0001274	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0001252	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0012806	OMIM:157170	IEA					P	HPO:skoehler[2018-10-08]
OMIM:157170	Holoprosencephaly 2		HP:0001290	OMIM:157170	TAS					P	HPO:skoehler[2017-07-13]
OMIM:157170	Holoprosencephaly 2		HP:0005273	OMIM:157170	IEA					P	HPO:iea[2009-02-17]
OMIM:157170	Holoprosencephaly 2		HP:0010941	PMID:10369266	PCS		1/4			P	HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0003829	OMIM:157170	IEA					I	HPO:skoehler[2010-06-19]
OMIM:157170	Holoprosencephaly 2		HP:0000612	PMID:10369266	PCS		1/4			P	HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000835	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0000873	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0003745	OMIM:157170	IEA					I	HPO:skoehler[2010-06-19]
OMIM:157170	Holoprosencephaly 2		HP:0002019	OMIM:157170	IEA					P	HPO:iea[2009-02-17]
OMIM:157170	Holoprosencephaly 2		HP:0001249	OMIM:157170	IEA					P	HPO:iea[2009-02-17]
OMIM:157170	Holoprosencephaly 2		HP:0006315	PMID:10369266	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000176	OMIM:157170	IEA					P	HPO:iea[2009-02-17]
OMIM:157170	Holoprosencephaly 2		HP:0000252	PMID:10369266	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0007968	PMID:10369266	PCS		1/4			P	HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0002650	OMIM:157170	IEA					P	HPO:iea[2009-02-17]
OMIM:157170	Holoprosencephaly 2		HP:0001321	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0001360	PMID:10369266	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000193	OMIM:157170	IEA					P	HPO:iea[2009-02-17]
OMIM:157170	Holoprosencephaly 2		HP:0001263	PMID:10369266	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000272	OMIM:157170	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157170	Holoprosencephaly 2		HP:0011800	PMID:10369266	PCS		1/4			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0010757	PMID:10369266	PCS		1/4			P	HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0100336	PMID:10369266	PCS		3/4			P	HPO:probinson[2024-03-08]
OMIM:157170	Holoprosencephaly 2		HP:0100337	PMID:10369266	PCS		3/4			P	HPO:probinson[2024-03-08]
OMIM:157170	Holoprosencephaly 2		HP:0009099	OMIM:157170	TAS					P	HPO:probinson[2024-03-29]
OMIM:157170	Holoprosencephaly 2		HP:0000601	PMID:10369266	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000568	PMID:10369266	PCS		1/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0002507	PMID:10369266	PCS		1/4			P	HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000520	PMID:10369266	PCS		2/4			P	HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000006	PMID:10369266	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:157170	Holoprosencephaly 2		HP:0000567	PMID:10369266	PCS		1/4			P	HPO:probinson[2022-09-02]
OMIM:105150	Amyloidosis VI		HP:0001342	OMIM:105150	TAS					P	HPO:skoehler[2015-01-21]
OMIM:105150	Amyloidosis VI		HP:0001297	OMIM:105150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:105150	Amyloidosis VI		HP:0000726	OMIM:105150	IEA					P	HPO:iea[2009-02-17]
OMIM:105150	Amyloidosis VI		HP:0002170	OMIM:105150	IEA					P	HPO:iea[2009-02-17]
OMIM:105150	Amyloidosis VI		HP:0000006	OMIM:105150	IEA					I	HPO:iea[2009-02-17]
OMIM:105150	Amyloidosis VI		HP:0003216	OMIM:105150	IEA					P	HPO:iea[2009-02-17]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0002908	OMIM:605479	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0003155	OMIM:605479	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0002240	OMIM:605479	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0001081	OMIM:605479	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0000007	OMIM:605479	IEA					I	HPO:skoehler[2010-06-19]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0000989	OMIM:605479	IEA					P	HPO:skoehler[2010-06-20]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0001406	OMIM:605479	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:605479	Cholestasis, benign recurrent intrahepatic, 2		HP:0000952	OMIM:605479	IEA					P	HPO:skoehler[2010-06-20]
OMIM:181250	Scalp defects and postaxial polydactyly		HP:0005696	OMIM:181250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:181250	Scalp defects and postaxial polydactyly		HP:0007385	OMIM:181250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:181250	Scalp defects and postaxial polydactyly		HP:0000006	OMIM:181250	TAS					I	HPO:skoehler[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0002311	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0000252	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0001297	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0003401	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0000708	OMIM:236250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0001288	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0002156	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0001250	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0001263	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0002160	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0000007	PMID:7920641	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-08-16]
OMIM:236250	Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolatereductase activity		HP:0001324	OMIM:236250	IEA					P	HPO:iea[2009-02-17]
OMIM:609257	Myopia 8		HP:0000545	OMIM:609257	TAS					P	HPO:skoehler[2014-10-17]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000286	OMIM:606164	TAS					P	HPO:skoehler[2015-12-30]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000494	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000175	PMID:24942156	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0003577	PMID:24942156	PCS		2/2			C	HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000475	PMID:24942156	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0004322	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0011968	OMIM:606164	TAS					P	HPO:skoehler[2015-12-30]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0002098	OMIM:606164	TAS					P	HPO:skoehler[2015-12-30]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000193	PMID:24942156	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0001263	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0002162	PMID:24942156	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0011800	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0045075	PMID:24942156	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000407	PMID:24942156	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0008551	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0001913	OMIM:606164	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0001972	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000410	OMIM:606164	TAS					P	HPO:skoehler[2015-12-30]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000006	PMID:24942156	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000776	PMID:24942156	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000347	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000358	PMID:24942156	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:606164	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis		HP:0000402	PMID:24942156	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:264270	Pseudohermaphroditism, female, with skeletal anomalies		HP:0000062	OMIM:264270	IEA					P	HPO:iea[2009-02-17]
OMIM:264270	Pseudohermaphroditism, female, with skeletal anomalies		HP:0000327	OMIM:264270	IEA					P	HPO:iea[2009-02-17]
OMIM:264270	Pseudohermaphroditism, female, with skeletal anomalies		HP:0000007	OMIM:264270	IEA					I	HPO:iea[2009-02-17]
OMIM:264270	Pseudohermaphroditism, female, with skeletal anomalies		HP:0005790	OMIM:264270	IEA					P	HPO:iea[2009-02-17]
OMIM:264270	Pseudohermaphroditism, female, with skeletal anomalies		HP:0008665	OMIM:264270	IEA					P	HPO:iea[2009-02-17]
OMIM:264270	Pseudohermaphroditism, female, with skeletal anomalies		HP:0005856	OMIM:264270	TAS					P	HPO:probinson[2009-02-17]
OMIM:264270	Pseudohermaphroditism, female, with skeletal anomalies		HP:0000786	OMIM:264270	IEA					P	HPO:iea[2009-02-17]
OMIM:619044	Spermatogenic failure 44		HP:0003251	PMID:31654588	IEA		2/2			P	HPO:probinson[2020-11-29]
OMIM:619044	Spermatogenic failure 44		HP:0030087	PMID:31654588	PCS		0/2			P	HPO:probinson[2020-11-29];HPO:probinson[2024-03-16]
OMIM:619044	Spermatogenic failure 44		HP:0000007	PMID:31654588	PCS					I	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619044	Spermatogenic failure 44		HP:0012207	PMID:31654588	PCS		2/2			P	HPO:probinson[2020-11-29]
OMIM:619044	Spermatogenic failure 44		HP:0012869	PMID:31654588	PCS		2/2			P	HPO:probinson[2020-11-29]
OMIM:619044	Spermatogenic failure 44		HP:0008734	PMID:31654588	PCS		0/2			P	HPO:probinson[2020-11-29];HPO:probinson[2024-03-16]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003202	PMID:21937588	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0002015	PMID:21937588	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003236	PMID:21937588	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003596	PMID:21937588	PCS		2/2			C	HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003200	PMID:21937588	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0000590	PMID:21937588	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0001260	PMID:21937588	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0002151	PMID:21937588	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003691	PMID:21937588	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0030319	PMID:21937588	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0009141	PMID:21937588	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0000508	PMID:21937588	PCS	HP:0003596	2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0000007	PMID:21937588	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003737	PMID:21937588	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003701	PMID:21937588	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617069	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3		HP:0003688	PMID:21937588	PCS		2/2			P	HPO:probinson[2023-03-06]
OMIM:608149	Kagami-Ogata syndrome		HP:0002089	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000343	OMIM:608149	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608149	Kagami-Ogata syndrome		HP:0000023	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000463	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001250	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001371	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001591	OMIM:608149	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608149	Kagami-Ogata syndrome		HP:0000581	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001252	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0002240	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0012745	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001290	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:608149	Kagami-Ogata syndrome		HP:0011335	OMIM:608149	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608149	Kagami-Ogata syndrome		HP:0001629	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0008551	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0100807	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001643	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0003745	OMIM:608149	TAS					I	HPO:skoehler[2015-12-30]
OMIM:608149	Kagami-Ogata syndrome		HP:0001642	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000278	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001744	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001601	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001622	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001540	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0002751	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000890	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001561	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0009826	OMIM:608149	TAS					P	HPO:skoehler[2015-06-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0002673	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001263	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0002092	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0005280	OMIM:608149	TAS					P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000327	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001539	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0002007	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0001631	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000883	OMIM:608149	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000347	OMIM:608149	TAS		12/20			P	HPO:skoehler[2015-02-22]
OMIM:608149	Kagami-Ogata syndrome		HP:0000006	OMIM:608149	IEA					I	HPO:skoehler[2019-04-18]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000494	PMID:18435799	PCS		3/4			P	HPO:probinson[2024-02-24]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0003577	PMID:17236138	PCS		9/9			C	HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000276	PMID:17236138	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0010609	OMIM:610706	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000691	PMID:17236138;PMID:18435799	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-06];HPO:probinson[2024-02-24];HPO:probinson[2024-02-24]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:6000376	PMID:18435799	PCS		3/4			P	HPO:probinson[2024-02-27]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0002194	PMID:17236138	PCS		9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0011476	PMID:17236138	PCS	HP:0003577	9/9			P	HPO:probinson[2012-07-16];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0040080	PMID:17236138;PMID:18435799	PCS		11/13			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-06];HPO:probinson[2024-02-24]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0011372	PMID:17236138	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0011266	PMID:17236138;PMID:18435799	PCS		13/13			P	HPO:probinson[2012-07-16];HPO:probinson[2022-08-06];HPO:probinson[2024-02-24]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0006342	PMID:17236138	PCS					P	HPO:probinson[2022-08-06];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000448	PMID:18435799	PCS		2/4			P	HPO:probinson[2024-02-24]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000007	PMID:17236138	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000347	PMID:17236138	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000687	PMID:17236138	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-06]
OMIM:610706	Deafness, congenital, with inner ear agenesis, microtia, and microdontia		HP:0000698	OMIM:610706	IEA					P	HPO:skoehler[2010-06-18]
OMIM:600273	Polycystic kidney disease, infantile severe, with tuberous sclerosis		HP:0009717	OMIM:600273	TAS					P	HPO:iea[2009-02-17]
OMIM:600273	Polycystic kidney disease, infantile severe, with tuberous sclerosis		HP:0006772	OMIM:600273	TAS					P	HPO:probinson[2014-01-18]
OMIM:600273	Polycystic kidney disease, infantile severe, with tuberous sclerosis		HP:0000113	OMIM:600273	TAS	HP:0003593				P	HPO:probinson[2014-01-18]
OMIM:600273	Polycystic kidney disease, infantile severe, with tuberous sclerosis		HP:0000006	OMIM:600273	TAS					I	HPO:iea[2014-01-18]
OMIM:616411	Dystonia 27		HP:0000473	PMID:26004199	PCS		5/5			P	HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0002345	PMID:26004199	PCS		1/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0002356	PMID:26004199	PCS		4/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0003621	PMID:26004199	PCS		1/5			C	HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0002451	PMID:26004199	PCS		2/5			P	HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0011462	PMID:26004199	PCS		4/5			C	HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0002174	PMID:26004199	PCS		2/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0000007	PMID:26004199	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0012048	PMID:26004199	PCS		3/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-13]
OMIM:616411	Dystonia 27		HP:0012049	PMID:26004199	PCS		2/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-10-13]
OMIM:613582	Retinitis pigmentosa 57		HP:0001133	PMID:20655036	PCS		4/4			P	HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0007737	PMID:20655036	PCS					P	HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0011463	PMID:20655036	PCS					C	HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0000007	PMID:20655036	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0007663	PMID:20655036	PCS		6/6			P	HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0011505	PMID:20655036	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0000543	PMID:20655036	PCS	HP:0011462				P	HPO:skoehler[2013-06-04];HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0000510	PMID:20655036	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0030825	PMID:20655036	PCS					P	HPO:probinson[2022-10-20]
OMIM:613582	Retinitis pigmentosa 57		HP:0007843	PMID:20655036	PCS	HP:0011462				P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:601186	Microphthalmia, syndromic 9		HP:0003510	PMID:17273977	PCS		1/3			P	HPO:probinson[2023-04-10]
OMIM:601186	Microphthalmia, syndromic 9		HP:0003577	PMID:17273977	PCS		2/3			C	HPO:probinson[2023-04-10]
OMIM:601186	Microphthalmia, syndromic 9		HP:0002089	OMIM:601186	TAS					P	HPO:probinson[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000023	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000089	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0004322	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001750	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0005311	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0005156	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000581	PMID:17273977	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001252	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000085	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001290	OMIM:601186	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601186	Microphthalmia, syndromic 9		HP:0033208	PMID:17273977	PCS		1/3			P	HPO:probinson[2023-04-10]
OMIM:601186	Microphthalmia, syndromic 9		HP:0006270	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001629	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000813	OMIM:601186	TAS					P	HPO:probinson[2012-07-15]
OMIM:601186	Microphthalmia, syndromic 9		HP:0004935	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001643	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001642	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0005944	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000776	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0004712	OMIM:601186	TAS					P	HPO:probinson[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001660	OMIM:601186	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000013	OMIM:601186	TAS					P	HPO:probinson[2012-07-15]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000431	PMID:17273977	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001680	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0020186	OMIM:601186	IEA					P	HPO:skoehler[2019-09-07]
OMIM:601186	Microphthalmia, syndromic 9		HP:0012736	PMID:17273977	PCS		1/3			P	HPO:probinson[2023-04-10]
OMIM:601186	Microphthalmia, syndromic 9		HP:0002093	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000528	PMID:17273977	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0009110	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0034198	PMID:17273977	PCS		1/3			C	HPO:probinson[2023-04-10]
OMIM:601186	Microphthalmia, syndromic 9		HP:0002627	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001636	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000007	PMID:17273977	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-10]
OMIM:601186	Microphthalmia, syndromic 9		HP:0007633	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001511	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0003811	PMID:17273977	PCS		1/3			C	HPO:probinson[2023-04-10]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000125	PMID:17273977	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0001631	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000028	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000369	PMID:17273977	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000347	PMID:17273977	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:601186	Microphthalmia, syndromic 9		HP:0000126	OMIM:601186	IEA					P	HPO:iea[2009-02-17]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0030007	PMID:31428396	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0003785	PMID:31922365	PCS		1/1			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0002069	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0002322	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0002312	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0000750	PMID:31428396;PMID:31922365	PCS		2/3			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0001256	PMID:31428396;PMID:31922365	PCS		3/3			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0002067	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0031825	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0001300	PMID:31922365	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0001332	PMID:31922365	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0001250	PMID:31428396	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0011968	PMID:31428396	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0002063	PMID:31922365	PCS		2/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0001263	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0003593	PMID:31428396	PCS		1/1			C	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0002174	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0034316	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-09-05]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0011463	PMID:31922365	PCS		2/2			C	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0011153	PMID:31428396	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0002304	PMID:31922365	PCS		1/2			P	HPO:probinson[2022-08-14]
OMIM:619911	Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism		HP:0000006	PMID:31428396	PCS					I	HPO:probinson[2022-08-14]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0003577	PMID:10053007;PMID:30152556	PCS		5/5			C	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0008064	PMID:30152556	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0008066	PMID:30152556	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0040189	PMID:10053007	PCS		4/4			P	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0010783	PMID:10053007	PCS	HP:0003577	4/4			P	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0040162	PMID:30152556	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0000972	PMID:10053007	PCS		4/4			P	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0000982	PMID:30152556	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0000006	PMID:10053007	PCS					I	HPO:probinson[2023-04-08]
OMIM:620148	Ichthyosis, annular epidermolytic 2		HP:0200041	PMID:10053007	PCS	HP:0003577	4/4			P	HPO:probinson[2023-04-08]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0002069	PMID:25066056	PCS		2/2			P	HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0008936	PMID:25066056	PCS		2/2			P	HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0003577	PMID:25066056	PCS		2/2			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0000252	PMID:25066056	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0000365	PMID:25066056	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0002650	PMID:25066056	PCS	HP:0003577	2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0002133	PMID:25066056	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0002120	PMID:25066056	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0001263	PMID:25066056	PCS		2/2		HP:0012829	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0001290	PMID:25066056	PCS	HP:0003577	2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0001508	PMID:25066056	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0034353	PMID:25066056	PCS		2/2			P	HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0100704	PMID:25066056	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0000998	PMID:25066056	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0007024	PMID:25066056	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0000007	PMID:25066056	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0001511	PMID:25066056	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0000543	PMID:25066056	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:617082	Congenital disorder of glycosylation, type IAA		HP:0007843	PMID:25066056	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0001022	OMIM:203200	TAS					P	HPO:skoehler[2015-01-21]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0000486	OMIM:203200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0005599	OMIM:203200	TAS					P	HPO:skoehler[2013-02-25]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0002297	OMIM:203200	TAS					P	HPO:skoehler[2010-06-20]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0001010	OMIM:203200	TAS					P	HPO:skoehler[2013-02-25]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0000639	OMIM:203200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0007750	OMIM:203200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0000635	OMIM:203200	TAS					P	HPO:skoehler[2013-02-25]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0000007	OMIM:203200	TAS					I	HPO:skoehler[2009-02-17]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0007894	OMIM:203200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0007663	OMIM:203200	TAS					P	HPO:skoehler[2015-07-26]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0000505	OMIM:203200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0000545	OMIM:203200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0007603	OMIM:203200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:203200	Albinism, oculocutaneous, type II		HP:0000577	OMIM:203200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0000252	OMIM:251220	IEA					P	HPO:iea[2009-02-17]
OMIM:251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0000007	OMIM:251220	IEA					I	HPO:iea[2009-02-17]
OMIM:251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0004209	OMIM:251220	IEA					P	HPO:iea[2009-02-17]
OMIM:251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0001852	OMIM:251220	IEA					P	HPO:iea[2009-02-17]
OMIM:251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0001249	OMIM:251220	IEA					P	HPO:iea[2009-02-17]
OMIM:251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0001644	OMIM:251220	IEA					P	HPO:iea[2009-02-17]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0003202	PMID:24482476	PCS		3/3			P	HPO:probinson[2017-06-25]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0003676	PMID:24482476	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0003621	PMID:24482476	PCS		1/7			C	HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0001288	PMID:24482476	PCS		7/7			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0003487	PMID:24482476	PCS		6/7			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0002395	PMID:24482476	PCS		6/7			P	HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0001260	PMID:24482476	PCS		1/7			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0002064	PMID:24482476	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0002061	PMID:24482476	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0002380	PMID:24482476	PCS		0/7			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0031993	PMID:24482476	PCS		0/7			P	HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0011448	PMID:24482476	PCS		2/7			P	HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0011463	PMID:24482476	PCS		6/7			C	HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0001317	PMID:24482476	PCS		3/3			P	HPO:probinson[2017-06-25]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0000007	PMID:24482476	PCS					I	HPO:probinson[2017-06-25]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0030051	PMID:24482476	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0002943	PMID:24482476	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0001257	PMID:24482476	PCS		7/7			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-15]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0001347	PMID:24482476	PCS		3/3			P	HPO:probinson[2017-06-25]
OMIM:615681	Spastic paraplegia 62, autosomal recessive		HP:0006844	PMID:24482476	PCS		1/7			P	HPO:skoehler[2017-07-13]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000341	PMID:24814191	PCS		1/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0002069	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0002521	PMID:24814191	PCS		1/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000463	PMID:24814191	PCS		2/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0002384	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0001252	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0003593	PMID:24814191	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0004381	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0012469	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0012110	PMID:24814191	PCS		2/3		HP:0012825	P	HPO:skoehler[2014-09-21];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0100704	PMID:24814191	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0012471	PMID:24814191	PCS		1/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000717	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000414	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000455	PMID:24814191	PCS		2/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000377	PMID:24814191	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000574	PMID:24814191	PCS		1/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0001344	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0002079	PMID:24814191	PCS		2/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000232	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0010819	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0001263	PMID:24814191	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000294	PMID:24814191	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0010730	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000506	PMID:24814191	PCS		2/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0032792	PMID:24814191	PCS		2/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000629	PMID:24814191	PCS		2/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000426	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000007	PMID:24814191	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000527	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0200134	PMID:24814191	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000664	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0000322	PMID:24814191	PCS		1/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-02-17]
OMIM:615859	Developmental and epileptic encephalopathy 23		HP:0001336	PMID:24814191	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:307700	Hypoparathyroidism, X-linked		HP:0000464	OMIM:307700	IEA					P	HPO:iea[2009-02-17]
OMIM:307700	Hypoparathyroidism, X-linked		HP:0001250	OMIM:307700	IEA					P	HPO:iea[2009-02-17]
OMIM:307700	Hypoparathyroidism, X-linked		HP:0008198	OMIM:307700	IEA					P	HPO:iea[2009-02-17]
OMIM:307700	Hypoparathyroidism, X-linked		HP:0001281	OMIM:307700	IEA					P	HPO:iea[2009-02-17]
OMIM:307700	Hypoparathyroidism, X-linked		HP:0001417	OMIM:307700	IEA					I	HPO:iea[2009-02-17]
OMIM:130100	Elastosis perforans serpiginosa		HP:0003764	OMIM:130100	IEA					P	HPO:skoehler[2009-02-17]
OMIM:130100	Elastosis perforans serpiginosa		HP:0000006	OMIM:130100	IEA					I	HPO:iea[2009-02-17]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0003577	PMID:15044640	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0033649	PMID:27516224	PCS		2/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0033542	PMID:27516224	PCS		7/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0001508	OMIM:610921	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0032980	PMID:27516224	PCS					P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002878	PMID:15044640	PCS	HP:0003623				P	HPO:skoehler[2014-06-24];HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0001522	PMID:15044640	PCS		2/21			C	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002875	PMID:27516224	PCS					P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0005942	PMID:15044640	PCS		4/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0025175	PMID:27516224	PCS		4/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0006517	PMID:15044640;OMIM:610921	PCS		18/19			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0025394	PMID:27516224	PCS		8/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002098	PMID:15044640	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0025179	PMID:27516224	PCS		11/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002094	PMID:27516224	PCS					P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0012735	PMID:27516224	PCS					P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0012418	PMID:27516224	PCS					P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0031950	PMID:27516224	PCS		1/23			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0025392	PMID:27516224	PCS		1/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0025391	PMID:27516224	PCS		2/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0025390	PMID:27516224	PCS		11/11			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0033584	PMID:27516224	PCS		7/23			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0000007	PMID:15044640	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0001217	PMID:27516224	PCS					P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0000961	PMID:27516224	PCS					P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0003811	PMID:15044640	PCS		11/21			C	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002206	PMID:27516224	PCS		2/23			P	HPO:probinson[2021-05-05]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002789	OMIM:610921	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002104	OMIM:610921	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		HP:0002643	PMID:27516224	PCS	HP:0003623	30/37			P	HPO:probinson[2021-05-05]
OMIM:608808	Transposition of the great arteries, dextro-looped 1		HP:0003829	OMIM:608808	TAS					I	HPO:skoehler[2017-07-13]
OMIM:608808	Transposition of the great arteries, dextro-looped 1		HP:0001669	PMID:14638541	PCS					P	HPO:probinson[2013-03-09]
OMIM:608808	Transposition of the great arteries, dextro-looped 1		HP:0000006	OMIM:608808	TAS					I	HPO:skoehler[2015-12-30]
OMIM:617928	Keratoconus 9		HP:0003621	PMID:29051577	PCS		2/2			C	HPO:probinson[2023-02-26]
OMIM:617928	Keratoconus 9		HP:0100689	PMID:29051577	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:617928	Keratoconus 9		HP:0000563	PMID:29051577	PCS		4/4			P	HPO:probinson[2023-02-26]
OMIM:617928	Keratoconus 9		HP:0007663	PMID:29051577	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-26]
OMIM:617928	Keratoconus 9		HP:0000006	PMID:29051577	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-26]
OMIM:179500	Raindrop hypopigmentation		HP:0001010	OMIM:179500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:179500	Raindrop hypopigmentation		HP:0000006	OMIM:179500	IEA					I	HPO:iea[2009-02-17]
OMIM:300709	X-LINKED intellectual disability, Shrimpton type		HP:0001249	OMIM:300709	IEA					P	HPO:skoehler[2015-01-27]
OMIM:134400	Factor V excess with spontaneous thrombosis		HP:0004950	OMIM:134400	TAS					P	HPO:iea[2009-02-17]
OMIM:134400	Factor V excess with spontaneous thrombosis		HP:0004419	OMIM:134400	TAS					P	HPO:iea[2009-02-17]
OMIM:134400	Factor V excess with spontaneous thrombosis		HP:0000006	OMIM:134400	TAS					I	HPO:iea[2009-02-17]
OMIM:134400	Factor V excess with spontaneous thrombosis		HP:0002204	OMIM:134400	TAS					P	HPO:iea[2009-02-17]
OMIM:134400	Factor V excess with spontaneous thrombosis		HP:0011996	OMIM:134400	TAS					P	HPO:iea[2012-07-21]
OMIM:143850	Orthostatic hypotensive disorder, Streeten type		HP:0001278	OMIM:143850	TAS					P	HPO:probinson[2009-02-17]
OMIM:143850	Orthostatic hypotensive disorder, Streeten type		HP:0001041	OMIM:143850	TAS					P	HPO:probinson[2009-02-17]
OMIM:143850	Orthostatic hypotensive disorder, Streeten type		HP:0000978	OMIM:143850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:143850	Orthostatic hypotensive disorder, Streeten type		HP:0001279	OMIM:143850	TAS					P	HPO:probinson[2009-02-17]
OMIM:143850	Orthostatic hypotensive disorder, Streeten type		HP:0000006	OMIM:143850	TAS					I	HPO:probinson[2009-02-17]
OMIM:105805	Aneurysm of interventricular septum		HP:0002617	OMIM:105805	IEA					P	HPO:skoehler[2010-06-20]
OMIM:105805	Aneurysm of interventricular septum		HP:0010438	OMIM:105805	IEA					P	HPO:skoehler[2010-06-20]
OMIM:105805	Aneurysm of interventricular septum		HP:0000006	OMIM:105805	IEA					I	HPO:iea[2009-02-17]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0001254	OMIM:617900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0001287	OMIM:617900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0003621	PMID:22851595	PCS		1/2			C	HPO:probinson[2022-03-27]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0001289	OMIM:617900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0002353	OMIM:617900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0003596	PMID:26513235	PCS		1/1			C	HPO:probinson[2022-03-27]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0001250	OMIM:617900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0003593	PMID:22851595	IEA		1/2			C	HPO:probinson[2022-03-27]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0012302	PMID:22851595;PMID:26513235	PCS		3/3			P	HPO:probinson[2022-03-27];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-27]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0003829	OMIM:617900	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0001269	OMIM:617900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0001268	OMIM:617900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617900	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8		HP:0000006	PMID:22851595	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-27]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0007979	PMID:36516086	PCS		65/119			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0000651	PMID:36516086	PCS		57/120			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0002321	PMID:36516086	PCS		33/114			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0001272	PMID:36516086	PCS		67/91			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0001260	PMID:36516086	PCS		63/118			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0002066	PMID:36516086	PCS		113/118			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0003581	PMID:36516086	PCS		122/122			C	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0002174	PMID:36516086	PCS		18/114			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0002070	PMID:36516086	PCS		94/118			P	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0000006	PMID:36516086	PCS					I	HPO:probinson[2023-03-12]
OMIM:620174	Spinocerebellar ataxia 27B, late-onset		HP:0010545	PMID:36516086	PCS		50/199			P	HPO:probinson[2023-03-12]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0002069	PMID:24747641	PCS		4/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0002133	PMID:24747641	PCS		4/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0001344	PMID:24747641	PCS		1/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0002373	PMID:24747641	PCS		5/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0002121	PMID:24747641	PCS		6/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0001251	PMID:24747641	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0003593	PMID:24747641	PCS		5/6			C	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0032794	PMID:24747641	PCS		4/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0011463	PMID:24747641	PCS		1/6			C	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0000729	PMID:24747641	PCS		4/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0020221	PMID:24747641	PCS		3/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0200134	PMID:24747641	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0007359	PMID:24747641	PCS		4/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0007018	PMID:24747641	PCS		1/6			P	HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0001249	PMID:24747641	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-09-22]
OMIM:615871	Epileptic encephalopathy, early infantile, 24		HP:0000006	PMID:24747641	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-22]
OMIM:300047	Intellectual developmental disorder, X-linked 20		HP:0001417	OMIM:300047	IEA					I	HPO:iea[2009-02-17]
OMIM:300047	Intellectual developmental disorder, X-linked 20		HP:0001249	OMIM:300047	IEA					P	HPO:iea[2009-02-17]
OMIM:158280	Motion sickness		HP:0000707	OMIM:158280	IEA					P	HPO:iea[2009-02-17]
OMIM:619093	Deafness, autosomal recessive 116		HP:0003621	PMID:31175426	PCS		3/3			C	HPO:probinson[2024-03-16]
OMIM:619093	Deafness, autosomal recessive 116		HP:0000407	PMID:31175426	PCS		3/3			P	HPO:probinson[2020-12-15]
OMIM:619093	Deafness, autosomal recessive 116		HP:0001263	PMID:31175426	PCS		0/3			P	HPO:probinson[2020-12-15];HPO:probinson[2024-03-16]
OMIM:619093	Deafness, autosomal recessive 116		HP:0000007	PMID:31175426	PCS					I	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619093	Deafness, autosomal recessive 116		HP:0002403	PMID:31175426	PCS		0/3			P	HPO:probinson[2024-03-16]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0003487	PMID:24388663	PCS		4/4			P	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0001288	PMID:24388663	PCS		2/4			P	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0002395	PMID:24388663	PCS		4/4			P	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0011463	PMID:24388663	PCS		4/4			C	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0001260	PMID:24388663	PCS		0/4			P	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0002066	PMID:24388663	PCS		0/4			P	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0002064	PMID:24388663	PCS		4/4			P	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0009046	PMID:24388663	PCS		2/2			P	HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0000007	PMID:24388663	PCS		20/20			I	HPO:probinson[2024-03-13]
OMIM:620606	Spastic paraplegia 72B, autosomal recessive		HP:0001257	PMID:24388663	PCS		4/4			P	HPO:probinson[2024-03-13]
OMIM:619087	Noonan syndrome 13		HP:0000286	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0002389	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001377	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0002020	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0010806	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001290	PMID:32721402	PCS		4/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000280	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000081	PMID:32721402	PCS		1/7		HP:0012833	P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0012469	PMID:32721402	PCS	HP:0003593	1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000958	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000957	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000718	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001609	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000635	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000316	PMID:32721402	PCS		5/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000998	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001845	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001004	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001840	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001763	PMID:32721402	PCS		3/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001249	PMID:32721402	PCS		6/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000358	PMID:32721402	PCS		6/7			P	HPO:probinson[2020-12-21];HPO:probinson[2023-02-06]
OMIM:619087	Noonan syndrome 13		HP:0002553	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000494	PMID:32721402	PCS		3/7			P	HPO:probinson[2020-12-21];HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000252	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0002230	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0002197	PMID:32721402	PCS	HP:0011463	1/5			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001382	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001263	PMID:32721402	PCS		7/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000691	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001182	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000403	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0007874	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001653	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000006	PMID:32721402	PCS					I	HPO:probinson[2022-09-04]
OMIM:619087	Noonan syndrome 13		HP:0000369	PMID:32721402	PCS		3/7			P	HPO:probinson[2023-02-06]
OMIM:619087	Noonan syndrome 13		HP:0001776	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000687	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000341	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000343	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000463	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0002162	PMID:32721402	PCS		4/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000739	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0100625	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000978	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0030084	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000218	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000154	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0025352	PMID:32721402	PCS					I	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000750	PMID:32721402	PCS		6/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001003	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0002650	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000431	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0005487	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000470	PMID:32721402	PCS		4/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0011229	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0012168	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0100559	PMID:32721402	PCS		1/7		HP:0012825	P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000508	PMID:32721402	PCS		6/7			P	HPO:probinson[2020-12-21];HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000348	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000307	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0002967	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001357	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001631	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0007018	PMID:32721402	PCS		3/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000465	PMID:32721402	PCS		4/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000028	PMID:32721402	PCS		2/6			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0000347	PMID:32721402	PCS		1/7			P	HPO:probinson[2020-12-21]
OMIM:619087	Noonan syndrome 13		HP:0001634	PMID:32721402	PCS		2/7			P	HPO:probinson[2020-12-21]
OMIM:202650	Agnathia-Otocephaly complex		HP:0008749	PMID:22211708	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0001696	PMID:22674740	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0009939	PMID:22674740;PMID:22211708;PMID:21294718	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0002089	PMID:22211708	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000160	PMID:22674740;PMID:21294718	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0001274	OMIM:202650	IEA					P	HPO:iea[2009-02-17]
OMIM:202650	Agnathia-Otocephaly complex		HP:0011461	PMID:22674740;PMID:22211708;PMID:21294718	PCS		3/3			C	HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0002779	PMID:22211708	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0005349	PMID:22211708	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000478	OMIM:202650	IEA					P	HPO:iea[2009-02-17]
OMIM:202650	Agnathia-Otocephaly complex		HP:0001561	PMID:22674740;PMID:21294718	PCS		2/2			P	HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000494	PMID:22674740;PMID:22211708	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000175	PMID:22674740	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0001684	PMID:22211708	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0002098	PMID:22674740	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0001360	OMIM:202650	IEA					P	HPO:iea[2009-02-17]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000171	PMID:22211708	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0012730	OMIM:202650	TAS					P	HPO:skoehler[2014-03-24]
OMIM:202650	Agnathia-Otocephaly complex		HP:0100663	PMID:22211708;PMID:21294718	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000007	PMID:22211708	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000405	OMIM:202650	IEA					P	HPO:iea[2009-02-17]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000347	OMIM:202650	IEA					P	HPO:iea[2009-02-17]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000006	PMID:21294718	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000369	PMID:22674740;PMID:21294718	PCS		2/2			P	HPO:probinson[2022-03-12]
OMIM:202650	Agnathia-Otocephaly complex		HP:0000445	PMID:22674740	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0002465	OMIM:617914	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000340	OMIM:617914	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000486	PMID:29343805	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000089	PMID:29343805	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0004322	OMIM:617914	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0001274	PMID:29343805	PCS		1/8			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0001290	OMIM:617914	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0045028	PMID:29343805	PCS		1/8			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0011463	PMID:29343805	PCS		5/8			C	HPO:probinson[2023-01-26];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000618	OMIM:617914	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0004719	OMIM:617914	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0002139	PMID:29343805	PCS		1/8			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0001249	OMIM:617914	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0003623	PMID:29343805	PCS		1/8			C	HPO:probinson[2023-01-26];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000252	PMID:29343805	PCS		7/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0010958	PMID:29343805	PCS		1/9			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000013	PMID:29343805	PCS		2/7			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0001321	PMID:29343805	PCS		2/8			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0002079	PMID:29343805	PCS		1/8			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0002472	OMIM:617914	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0002194	PMID:29343805	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000609	PMID:29343805	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0012300	PMID:29343805	PCS		2/9			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0034198	PMID:29343805	PCS		2/8			C	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000007	PMID:29343805	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000568	PMID:29343805	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0001511	PMID:29343805	PCS		2/9			P	HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0007018	PMID:29343805	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0009879	OMIM:617914	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617914	Microcephaly 20, primary, autosomal recessive		HP:0000148	PMID:29343805	PCS		1/7			P	HPO:probinson[2023-01-26]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000220	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000286	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000252	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000494	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000750	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0001252	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0001263	OMIM:608363	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0001290	OMIM:608363	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000316	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0001328	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0030680	OMIM:608363	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000218	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0003745	OMIM:608363	IEA					I	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000377	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0001510	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000006	OMIM:608363	IEA					I	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000347	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000369	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0000457	OMIM:608363	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0001249	OMIM:608363	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608363	Chromosome 22q11.2 duplication syndrome		HP:0001611	OMIM:608363	IEA					P	HPO:skoehler[2010-06-19]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0002465	PMID:30401461	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0002069	PMID:30100084	PCS		13/16			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000486	PMID:30401461	PCS		2/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001310	PMID:30100084	PCS		3/16			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001272	PMID:30100084	PCS		4/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001250	PMID:30401461	PCS		6/11			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0002121	PMID:30100084	PCS		3/16			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001251	PMID:30401461	PCS		11/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0002080	PMID:30401461	PCS		1/12			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000639	PMID:30401461	PCS		3/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0011463	PMID:30100084	PCS		16/16			C	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001308	PMID:30100084	PCS		2/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001324	PMID:30100084	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0003447	PMID:30401461	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0006855	PMID:30100084	PCS		2/9			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0002059	PMID:30100084	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000252	PMID:30401461	PCS		3/5			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000651	PMID:30401461	PCS		1/11			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0003487	PMID:30401461	PCS		1/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0002376	PMID:30100084	PCS		10/16			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001761	PMID:30100084	PCS		1/16			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001260	PMID:30401461	PCS		1/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0001263	PMID:30401461	PCS		10/12			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0002093	PMID:30401461	PCS		6/12			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000407	PMID:30100084;PMID:30401461	PCS		3/25			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000508	PMID:30401461	PCS		1/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0031165	PMID:30100084	PCS		2/16			P	HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000602	PMID:30401461	PCS		1/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-21]
OMIM:618170	Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures		HP:0000007	PMID:30100084	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-21]
OMIM:617243	Fanconi anemia, complementation group V		HP:0000252	PMID:27500492	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0004322	PMID:27500492	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0001903	PMID:27500492	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0011463	PMID:27500492	PCS		1/1			C	HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0003221	PMID:27500492	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0006254	PMID:27500492	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0000007	PMID:27500492	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0005528	PMID:27500492	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0001873	PMID:27500492	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617243	Fanconi anemia, complementation group V		HP:0001875	PMID:27500492	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:277740	White forelock with malformations		HP:0002211	OMIM:277740	IEA					P	HPO:iea[2009-02-17]
OMIM:277740	White forelock with malformations		HP:0002780	OMIM:277740	TAS					P	HPO:skoehler[2009-02-17]
OMIM:277740	White forelock with malformations		HP:0010185	OMIM:277740	IEA					P	HPO:iea[2009-02-17]
OMIM:277740	White forelock with malformations		HP:0000316	OMIM:277740	IEA					P	HPO:iea[2009-02-17]
OMIM:277740	White forelock with malformations		HP:0000007	OMIM:277740	IEA					I	HPO:iea[2009-02-17]
OMIM:277740	White forelock with malformations		HP:0002290	OMIM:277740	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277740	White forelock with malformations		HP:0007457	OMIM:277740	IEA					P	HPO:iea[2009-02-17]
OMIM:277740	White forelock with malformations		HP:0001631	OMIM:277740	IEA					P	HPO:iea[2009-02-17]
OMIM:604559	Progressive familial heart block, type IB		HP:0001662	OMIM:604559	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604559	Progressive familial heart block, type IB		HP:0005165	OMIM:604559	TAS					P	HPO:probinson[2013-04-07]
OMIM:604559	Progressive familial heart block, type IB		HP:0011711	OMIM:604559	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604559	Progressive familial heart block, type IB		HP:0001657	PMID:19726882	PCS		6/71			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-07-16]
OMIM:604559	Progressive familial heart block, type IB		HP:0011712	OMIM:604559	IEA		19/71			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:604559	Progressive familial heart block, type IB		HP:0011675	PMID:19726882	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:604559	Progressive familial heart block, type IB		HP:0001279	OMIM:604559	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604559	Progressive familial heart block, type IB		HP:0001678	PMID:19726882	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-16]
OMIM:604559	Progressive familial heart block, type IB		HP:0000006	PMID:19726882	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:613743	Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete		HP:0012245	OMIM:613743	TAS					P	HPO:probinson[2013-08-10]
OMIM:613743	Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete		HP:0000859	OMIM:613743	TAS					P	HPO:probinson[2013-08-10]
OMIM:613743	Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete		HP:0011749	OMIM:613743	TAS					P	HPO:probinson[2013-08-10]
OMIM:613743	Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete		HP:0000953	OMIM:613743	TAS					P	HPO:probinson[2013-08-10]
OMIM:613743	Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete		HP:0000846	OMIM:613743	IEA					P	HPO:skoehler[2015-01-19]
OMIM:613743	Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete		HP:0000127	OMIM:613743	TAS					P	HPO:probinson[2013-08-10]
OMIM:190605	Triphalangeal thumb-polysyndactyly syndrome		HP:0001199	PMID:18178630	PCS		11/12			P	HPO:probinson[2023-07-09]
OMIM:190605	Triphalangeal thumb-polysyndactyly syndrome		HP:0001177	PMID:18178630	PCS		3/12			P	HPO:probinson[2023-07-09]
OMIM:190605	Triphalangeal thumb-polysyndactyly syndrome		HP:0003577	PMID:18178630	PCS		12/12			C	HPO:probinson[2023-07-09]
OMIM:190605	Triphalangeal thumb-polysyndactyly syndrome		HP:0001162	PMID:18178630	PCS		4/12			P	HPO:probinson[2023-07-09]
OMIM:190605	Triphalangeal thumb-polysyndactyly syndrome		HP:0006101	PMID:18178630	PCS		5/12			P	HPO:probinson[2023-07-09]
OMIM:190605	Triphalangeal thumb-polysyndactyly syndrome		HP:0000006	PMID:18178630	PCS					I	HPO:probinson[2023-07-09]
OMIM:190605	Triphalangeal thumb-polysyndactyly syndrome		HP:0011304	PMID:18178630	PCS		2/12			P	HPO:probinson[2023-07-09]
OMIM:152550	Lumbar stenosis, familial		HP:0004610	OMIM:152550	IEA					P	HPO:iea[2009-02-17]
OMIM:152550	Lumbar stenosis, familial		HP:0000006	OMIM:152550	IEA					I	HPO:iea[2009-02-17]
OMIM:125900	Diastema, dental medial		HP:0001566	OMIM:125900	IEA					P	HPO:iea[2009-02-17]
OMIM:125900	Diastema, dental medial		HP:0000006	OMIM:125900	IEA					I	HPO:iea[2009-02-17]
OMIM:125900	Diastema, dental medial		HP:0000699	OMIM:125900	TAS					P	HPO:probinson[2009-02-17]
OMIM:168800	Parotidomegaly, hereditary bilateral		HP:0000464	OMIM:168800	IEA					P	HPO:iea[2009-02-17]
OMIM:168800	Parotidomegaly, hereditary bilateral		HP:0000006	OMIM:168800	IEA					I	HPO:iea[2009-02-17]
OMIM:621097	Immunodeficiency 131		HP:6001166	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0025021	PMID:29537367	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002583	PMID:36662884	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0030374	PMID:36662884	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0003593	PMID:36917008;PMID:36662884	PCS		10/10			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0410392	PMID:36917008	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0032436	PMID:29537367	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0033207	PMID:36917008	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0032163	PMID:36917008	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0011462	PMID:29537367	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0030381	PMID:36662884	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002216	PMID:36917008	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:4000007	PMID:36662884	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001369	PMID:29537367;PMID:36662884	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0003623	PMID:29408330	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002037	PMID:36917008	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0020086	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0030388	PMID:36662884	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002110	PMID:36662884	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0025092	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0005186	PMID:29537367	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0012418	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:6000647	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0100776	PMID:36917008	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0032170	PMID:36917008	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002829	PMID:29537367	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0032252	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0032132	PMID:36662884;PMID:29408330	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000403	PMID:36917008	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000964	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000007	PMID:29408330	PCS					I	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0200034	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002027	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000006	PMID:36917008	PCS					I	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002028	PMID:36917008;PMID:36662884	PCS		5/9			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0020071	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0005479	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001036	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0020072	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000265	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0005353	PMID:36917008	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0004385	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002240	PMID:36662884	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0010783	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0012203	PMID:36917008;PMID:36662884	PCS		3/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0011950	PMID:36662884	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0032261	PMID:36662884	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002719	PMID:36662884	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001508	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001943	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000975	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002716	PMID:36662884	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002878	PMID:36662884	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0020102	PMID:36662884	PCS		6/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0006532	PMID:36662884	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001744	PMID:36662884	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:6000263	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002014	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002850	PMID:36662884;PMID:29408330	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001880	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0004432	PMID:36662884	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0011703	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0031378	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0012115	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0033117	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0011108	PMID:36662884	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0010976	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0031458	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000509	PMID:36917008	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0040089	PMID:36917008	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001954	PMID:29408330	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0000988	PMID:36662884	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002205	PMID:36662884	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0001433	PMID:36917008	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0002720	PMID:36662884;PMID:29408330	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621097	Immunodeficiency 131		HP:0003139	PMID:36917008	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:600059	Retinitis pigmentosa 13		HP:0001133	PMID:22039234	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0007737	PMID:22039234	PCS					P	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0003621	PMID:22039234	PCS					C	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0000662	PMID:22039234	PCS	HP:0003621	9/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0030672	PMID:22039234	PCS		1/11			P	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0012426	PMID:22039234	PCS		1/7			P	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0030629	PMID:22039234	PCS		2/7			P	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0011505	PMID:22039234	PCS		4/7			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0011463	PMID:22039234	PCS					C	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0011462	PMID:22039234	PCS					C	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0003829	PMID:22039234	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0000546	PMID:22039234	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0000510	PMID:22039234	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0007843	PMID:22039234	PCS					P	HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0000006	PMID:11468273	PCS					I	HPO:probinson[2015-07-19];HPO:probinson[2022-10-07]
OMIM:600059	Retinitis pigmentosa 13		HP:0000523	PMID:22039234	PCS		4/11			P	HPO:probinson[2022-10-07]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0025114	PMID:25398053	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0003593	PMID:25398053	PCS		3/3			C	HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0025092	PMID:25398053	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0010783	PMID:25398053	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0040162	PMID:25398053	PCS		3/3			P	HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0000982	PMID:25398053	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0000006	PMID:25398053	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0000962	PMID:25398053	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:617525	Erythrokeratodermia variabilis et progressiva 3		HP:0001820	PMID:25398053	PCS		3/3			P	HPO:probinson[2023-05-21]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0001771	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002421	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0008947	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003731	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003551	PMID:29178646	PCS		4/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003691	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0001252	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003593	PMID:29178646;PMID:35510366	PCS		3/10			C	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0001270	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003391	PMID:29178646	PCS		3/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0030319	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0007340	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0011462	PMID:29178646	PCS		1/8			C	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0009046	PMID:29178646;PMID:35510366	PCS		2/11			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0009027	PMID:29178646	PCS		2/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003749	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003307	PMID:29178646;PMID:35510366	PCS		2/11			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002515	PMID:29178646	PCS		3/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0000218	PMID:29178646;PMID:35510366	PCS		6/11			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003803	PMID:29178646;PMID:35510366	PCS		5/10			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003701	PMID:29178646;PMID:35510366	PCS		5/11			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003547	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002058	PMID:29178646	PCS		3/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003202	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002015	PMID:29178646	PCS		3/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003621	PMID:29178646	PCS		6/8			C	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002870	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002650	PMID:29178646;PMID:35510366	PCS		4/11			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002474	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0001288	PMID:29178646	PCS		2/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0000276	PMID:29178646;PMID:35510366	PCS		2/11			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0001761	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0011968	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0001284	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0002093	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0000768	PMID:29178646	PCS		3/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0030051	PMID:29178646	PCS		1/9			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0001533	PMID:35510366	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0000006	PMID:29178646	PCS					I	HPO:probinson[2023-07-14]
OMIM:620389	Nemaline myopathy 5C, autosomal dominant		HP:0003798	PMID:29178646;PMID:35510366	PCS		8/10			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0003378	PMID:10071056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0001265	OMIM:607736	IEA					P	HPO:iea[2009-02-17]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0002015	OMIM:607736	IEA					P	HPO:iea[2009-02-17]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0003376	OMIM:607736	IEA					P	HPO:iea[2009-02-17]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0003596	PMID:10071056	PCS					C	HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0001761	PMID:10071056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0003693	PMID:10071056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0030211	PMID:10071056	PCS					P	HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0001284	PMID:10071056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0002460	PMID:10071056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0011096	OMIM:607736	PCS	HP:0003581				P	HPO:probinson[2012-04-11]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0000408	OMIM:607736	IEA					P	HPO:iea[2009-02-17]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0000407	OMIM:607736	PCS					P	HPO:probinson[2012-04-11]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0033362	PMID:15159512	PCS		1/1			P	HPO:probinson[2021-02-13]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0009027	PMID:10071056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-12-02]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0002936	OMIM:607736	IEA					P	HPO:iea[2009-02-17]
OMIM:607736	Charcot-Marie-Tooth disease, type 2J		HP:0000006	PMID:10071056	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-12-02]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000046	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000365	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0002221	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000343	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000485	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001156	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001250	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000160	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0003196	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001252	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001290	OMIM:601353	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0012368	OMIM:601353	TAS					P	HPO:skoehler[2013-10-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000917	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000518	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000915	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0008551	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000316	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000219	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0003745	OMIM:601353	IEA					I	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0040019	OMIM:601353	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000358	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001249	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000175	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000494	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0002059	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0002650	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0002079	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0003187	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001263	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000272	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001182	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0005280	OMIM:601353	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0012385	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001838	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000007	OMIM:601353	TAS					I	HPO:skoehler[2015-12-30]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000527	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000586	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0001510	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000248	OMIM:601353	IEA					P	HPO:iea[2009-02-17]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000028	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000369	OMIM:601353	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601353	Brachycephaly, deafness, cataract, microstomia, and impaired intellectual development		HP:0000049	OMIM:601353	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:613757	Macular degeneration, age-related, 6		HP:0000608	OMIM:613757	TAS					P	HPO:probinson[2013-01-09]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0000286	OMIM:614038	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0001182	OMIM:614038	TAS		HP:0040283			P	HPO:skoehler[2013-04-09]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0001909	OMIM:614038	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0033222	PMID:21892158	PCS		4/14			P	HPO:probinson[2022-09-06]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0004808	PMID:21892158	PCS		6/14			P	HPO:probinson[2022-09-06]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0100658	OMIM:614038	TAS				HP:0031796	P	HPO:skoehler[2013-06-06]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0000601	OMIM:614038	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0100807	OMIM:614038	TAS		HP:0040283			P	HPO:skoehler[2013-04-09]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0001004	PMID:21892158	PCS		13/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-06]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0000465	OMIM:614038	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0200043	PMID:21892158	PCS		4/14			P	HPO:probinson[2022-09-06]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0000006	PMID:21892158	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-06]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0002863	PMID:21892158	PCS		7/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-06]
OMIM:614038	Lymphedema, primary, with myelodysplasia		HP:0001876	OMIM:614038	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261650	Phosphoenolpyruvate carboxykinase 2, mitochondrial		HP:0001397	OMIM:261650	IEA					P	HPO:iea[2009-02-17]
OMIM:261650	Phosphoenolpyruvate carboxykinase 2, mitochondrial		HP:0001399	OMIM:261650	IEA					P	HPO:iea[2009-02-17]
OMIM:261650	Phosphoenolpyruvate carboxykinase 2, mitochondrial		HP:0000007	OMIM:261650	IEA					I	HPO:iea[2009-02-17]
OMIM:261650	Phosphoenolpyruvate carboxykinase 2, mitochondrial		HP:0000799	OMIM:261650	IEA					P	HPO:iea[2009-02-17]
OMIM:261650	Phosphoenolpyruvate carboxykinase 2, mitochondrial		HP:0001943	OMIM:261650	IEA					P	HPO:iea[2009-02-17]
OMIM:261650	Phosphoenolpyruvate carboxykinase 2, mitochondrial		HP:0005959	OMIM:261650	IEA					P	HPO:iea[2009-02-17]
DECIPHER:2	Cri du Chat Syndrome (5p deletion)		HP:0000252	DECIPHER:2	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:2	Cri du Chat Syndrome (5p deletion)		HP:0001620	DECIPHER:2	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:2	Cri du Chat Syndrome (5p deletion)		HP:0001249	DECIPHER:2	IEA					P	HPO:skoehler[2013-05-29]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0000252	PMID:23849775	PCS		1/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0001263	PMID:23849775	PCS		3/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0001252	PMID:23849775	PCS		3/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0003593	PMID:23849775	PCS		5/5			C	HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0011923	PMID:23849775	PCS		4/4			P	HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0003819	PMID:23849775	PCS		1/5			C	HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0001508	PMID:23849775	PCS		1/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0001639	PMID:23849775	PCS		5/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0000407	PMID:23849775	PCS		1/5			P	HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0000007	PMID:23849775	PCS					I	HPO:skoehler[2013-10-22];HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0001635	PMID:23849775	PCS		3/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0008897	PMID:23849775	PCS		1/5			P	HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0001522	PMID:23849775	PCS		2/5			C	HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0001511	PMID:23849775	PCS		2/5			P	HPO:probinson[2023-04-03]
OMIM:615440	Combined oxidative phosphorylation deficiency 17		HP:0003128	PMID:23849775	PCS		3/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-04-03]
OMIM:228250	Femur, unilateral bifid, with monodactylous ectrodactyly		HP:0004058	OMIM:228250	TAS					P	HPO:skoehler[2010-06-20]
OMIM:228250	Femur, unilateral bifid, with monodactylous ectrodactyly		HP:0003982	OMIM:228250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:228250	Femur, unilateral bifid, with monodactylous ectrodactyly		HP:0000007	OMIM:228250	TAS					I	HPO:probinson[2009-02-17]
OMIM:228250	Femur, unilateral bifid, with monodactylous ectrodactyly		HP:0001171	OMIM:228250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:228250	Femur, unilateral bifid, with monodactylous ectrodactyly		HP:0010443	OMIM:228250	TAS					P	HPO:probinson[2013-12-15]
OMIM:228250	Femur, unilateral bifid, with monodactylous ectrodactyly		HP:0009556	OMIM:228250	TAS					P	HPO:skoehler[2013-10-22]
OMIM:228250	Femur, unilateral bifid, with monodactylous ectrodactyly		HP:0200054	OMIM:228250	TAS					P	HPO:probinson[2013-12-15]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000286	PMID:29961569;PMID:32376980	PCS		25/49			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001650	PMID:29961569	PCS		1/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0004325	PMID:32376980	PCS		5/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000365	PMID:29961569;PMID:32376980	PCS		26/49			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002144	PMID:29961569	PCS		3/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000486	PMID:32376980	PCS		10/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0004322	PMID:32376980	PCS		12/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001250	PMID:29961569;PMID:32376980	PCS		9/49			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001252	PMID:29961569;PMID:32376980	PCS		19/49			P	HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0003593	PMID:29961569	PCS		1/7			C	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0009465	PMID:32376980	PCS		4/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000316	PMID:32376980	PCS		17/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001845	PMID:32376980	PCS		10/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001647	PMID:32376980	PCS		6/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0009466	PMID:32376980	PCS		6/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001847	PMID:32376980	PCS		4/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001643	PMID:29961569;PMID:32376980	PCS		28/49			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000476	PMID:29961569	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001763	PMID:32376980	PCS		10/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001249	PMID:32376980	PCS		23/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0003623	PMID:29961569	PCS		1/7			C	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002036	PMID:32376980	PCS		1/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000252	PMID:32376980	PCS		5/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002750	PMID:32376980	PCS		4/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0011968	PMID:29961569;PMID:32376980	PCS		27/49			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001382	PMID:32376980	PCS		4/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001263	PMID:29961569	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0034349	PMID:29961569	PCS		1/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0034392	PMID:32376980	PCS		8/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000729	PMID:32376980	PCS		6/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001537	PMID:29961569;PMID:32376980	PCS		6/49			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000648	PMID:29961569	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000768	PMID:32376980	PCS		17/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001852	PMID:32376980	PCS		5/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000006	PMID:29961569	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000369	PMID:29961569	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001276	PMID:29961569	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0003577	PMID:29961569	PCS		5/7			C	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000463	PMID:32376980	PCS		7/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000023	PMID:32376980	PCS		7/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001195	PMID:29961569	PCS		2/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000581	PMID:32376980	PCS		33/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0004383	PMID:29961569	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0010741	PMID:32376980	PCS		3/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001270	PMID:29961569;PMID:32376980	PCS		34/47			P	HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001629	PMID:32376980	PCS		6/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002719	PMID:32376980	PCS		4/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0100704	PMID:29961569	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0011560	PMID:29961569	PCS		1/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000414	PMID:32376980	PCS		17/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002119	PMID:29961569	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0030084	PMID:29961569	PCS		3/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0004935	PMID:29961569	PCS		1/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0006610	PMID:29961569	PCS		5/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0005989	PMID:29961569	PCS		1/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000256	PMID:32376980	PCS		5/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001622	PMID:32376980	PCS		10/42			P	HPO:probinson[2024-01-04];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002059	PMID:29961569	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001363	PMID:32376980	PCS		3/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000750	PMID:29961569;PMID:32376980	PCS		33/47			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002650	PMID:32376980	PCS		7/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000474	PMID:29961569	PCS		5/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0010813	PMID:29961569	PCS		3/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001680	PMID:29961569	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000470	PMID:32376980	PCS		24/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0003186	PMID:32376980	PCS		6/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0032152	PMID:32376980	PCS		3/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000506	PMID:32376980	PCS		14/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001719	PMID:29961569	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0000508	PMID:29961569;PMID:32376980	PCS		23/49			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-21];HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001511	PMID:29961569	PCS		1/7			P	HPO:probinson[2023-02-21]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001159	PMID:32376980	PCS		5/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0001631	PMID:32376980	PCS		9/42			P	HPO:probinson[2024-01-04]
OMIM:618164	Cardiac, facial, and digital anomalies with developmental delay		HP:0002643	PMID:29961569	PCS		4/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001250	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001371	PMID:15543146	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0003074	PMID:15543146	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0012642	PMID:15543146	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000819	OMIM:609069	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001508	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001903	OMIM:609069	IEA					P	HPO:skoehler[2019-09-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0100801	PMID:15543146	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001943	OMIM:609069	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001522	PMID:15543146	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000377	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0002335	PMID:15543146	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001265	OMIM:609069	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000252	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000331	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001684	OMIM:609069	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001387	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0001321	OMIM:609069	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0002594	OMIM:609069	IEA					P	HPO:skoehler[2019-09-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0010557	OMIM:609069	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000609	PMID:15543146	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000007	PMID:15543146	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0003758	PMID:15543146	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000768	OMIM:609069	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000444	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000325	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0008846	PMID:15543146	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0000369	OMIM:609069	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609069	Pancreatic and cerebellar agenesis		HP:0002104	OMIM:609069	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602114	Nephropathy, progressive tubulointerstitial, with cholestatic liverdisease		HP:0000112	OMIM:602114	IEA					P	HPO:skoehler[2015-01-27]
OMIM:602114	Nephropathy, progressive tubulointerstitial, with cholestatic liverdisease		HP:0001969	OMIM:602114	IEA					P	HPO:iea[2009-02-17]
OMIM:602114	Nephropathy, progressive tubulointerstitial, with cholestatic liverdisease		HP:0000007	OMIM:602114	IEA					I	HPO:iea[2009-02-17]
OMIM:602114	Nephropathy, progressive tubulointerstitial, with cholestatic liverdisease		HP:0002910	OMIM:602114	IEA					P	HPO:iea[2009-02-17]
OMIM:602114	Nephropathy, progressive tubulointerstitial, with cholestatic liverdisease		HP:0012622	OMIM:602114	TAS					P	HPO:probinson[2014-01-18]
OMIM:602114	Nephropathy, progressive tubulointerstitial, with cholestatic liverdisease		HP:0002611	OMIM:602114	IEA					P	HPO:iea[2009-02-17]
OMIM:615468	Immunodeficiency 12		HP:0004325	PMID:24332264	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0002750	PMID:24332264	PCS		1/1			P	HPO:skoehler[2014-06-24]
OMIM:615468	Immunodeficiency 12		HP:0000265	PMID:23727036	PCS		2/2			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0002783	PMID:23727036	PCS	HP:0003593	2/2			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0002783	PMID:24332264	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0004322	PMID:24332264	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0002043	PMID:24332264	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0002110	PMID:23727036;PMID:24332264	PCS		3/3			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0410295	PMID:23727036	PCS		2/2			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0003593	PMID:23727036;PMID:24332264	PCS		3/3			C	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0410293	PMID:23727036	PCS		2/2			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0011421	PMID:23727036	PCS		2/2			C	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0011107	PMID:23727036	PCS		2/2			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0000939	PMID:24332264	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0040088	PMID:23727036	PCS		0/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0031382	PMID:23727036	PCS		2/2			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0100825	PMID:24332264	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0002718	PMID:23727036	PCS		2/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0000007	PMID:23727036	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0001217	PMID:24332264	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0004429	PMID:24332264	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0000988	PMID:24332264	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0001510	PMID:23727036	PCS		2/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-05-08]
OMIM:615468	Immunodeficiency 12		HP:0002721	PMID:23727036	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-05-08]
OMIM:232220	Glycogen storage disease Ib		HP:0000660	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0004322	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0003077	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0002240	PMID:32838757	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:232220	Glycogen storage disease Ib		HP:0003593	PMID:32838757	PCS		1/1			C	HPO:probinson[2022-08-07]
OMIM:232220	Glycogen storage disease Ib		HP:0000939	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0002718	PMID:32838757	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:232220	Glycogen storage disease Ib		HP:0001943	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0002910	OMIM:232220	PCS				HP:0012825	P	HPO:probinson[2012-03-18]
OMIM:232220	Glycogen storage disease Ib		HP:0001744	PMID:32838757	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:232220	Glycogen storage disease Ib		HP:0001402	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0003128	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0002037	PMID:32838757	PCS	HP:0003621	1/1			P	HPO:probinson[2022-08-07]
OMIM:232220	Glycogen storage disease Ib		HP:0000155	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0000991	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:6000201	PMID:9428641	PCS		2/2			P	HPO:probinson[2024-02-27]
OMIM:232220	Glycogen storage disease Ib		HP:0000295	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0000097	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0000093	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0012213	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0100732	PMID:32838757	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:232220	Glycogen storage disease Ib		HP:0000822	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0000007	PMID:9428641	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:232220	Glycogen storage disease Ib		HP:0000823	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0001538	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0001114	OMIM:232220	TAS					P	HPO:skoehler[2017-07-13]
OMIM:232220	Glycogen storage disease Ib		HP:0000105	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0001997	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0000787	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0001733	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0002149	OMIM:232220	IEA					P	HPO:iea[2009-02-17]
OMIM:232220	Glycogen storage disease Ib		HP:0001875	PMID:9428641;PMID:32838757	PCS		34/34			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0003487	OMIM:609041	IEA					P	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0002395	OMIM:609041	IEA					P	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0001260	OMIM:609041	IEA					P	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0006938	OMIM:609041	IEA					P	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0003581	OMIM:609041	IEA					C	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0002061	OMIM:609041	IEA					P	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0005340	OMIM:609041	IEA					P	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0000007	OMIM:609041	IEA					I	HPO:iea[2009-02-17]
OMIM:609041	Spastic paraplegia 27, autosomal recessive		HP:0001258	OMIM:609041	TAS					P	HPO:skoehler[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002663	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002982	OMIM:264700	TAS					P	HPO:probinson[2012-05-01]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0000684	PMID:26734137	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002980	OMIM:264700	TAS					P	HPO:probinson[2012-05-01]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003155	PMID:26734137	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0001252	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0003593	PMID:26734137	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0001290	OMIM:264700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0009023	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0011463	PMID:9486994	PCS		4/4			C	HPO:probinson[2023-02-26]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002979	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0000117	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0008897	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0001324	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003029	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003106	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0005469	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002752	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0000893	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002199	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003165	PMID:26734137	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0004492	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002909	PMID:26734137	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002748	PMID:26734137;PMID:9486994	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0000007	PMID:9486994	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0000920	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0003758	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002901	PMID:26734137;PMID:9486994	PCS		5/5			P	HPO:probinson[2023-02-26];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0001538	OMIM:264700	TAS					P	HPO:probinson[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0000886	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002148	PMID:26734137;OMIM:264700	PCS		11/11			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003698	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003013	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0001270	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0010502	OMIM:264700	TAS					P	HPO:probinson[2012-05-01]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0002919	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0001508	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0000737	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0012052	PMID:26734137;PMID:9486994	PCS		5/5			P	HPO:probinson[2023-02-26];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0012053	PMID:9486994	PCS		0/4			P	HPO:probinson[2023-02-26]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0006297	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002757	PMID:26734137	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-14]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0003127	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0001942	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0000897	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002753	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002653	PMID:26734137	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0001288	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003025	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0003020	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0003021	PMID:26734137	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D-dependent rickets, type I		HP:0011422	PMID:26734137	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0000867	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0002007	OMIM:264700	IEA					P	HPO:iea[2009-02-17]
OMIM:264700	Vitamin D hydroxylation-deficient rickets, type 1A		HP:0001510	OMIM:264700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0002036	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0002169	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0000012	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0001761	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0002013	OMIM:609727	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0003487	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0002495	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0003265	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0000020	OMIM:609727	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0002061	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0000407	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0000019	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0000752	OMIM:609727	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0001258	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0000006	OMIM:609727	IEA					I	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0000017	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0003743	OMIM:609727	IEA					I	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0006986	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:609727	Spastic paraplegia 29, autosomal dominant		HP:0001347	OMIM:609727	IEA					P	HPO:iea[2009-02-17]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000365	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001696	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001695	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002783	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0004322	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000083	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003593	PMID:31595528	PCS		2/6			C	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002020	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003073	PMID:31595528	PCS		5/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0010445	PMID:34177428;PMID:31595528	PCS		2/7			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0010442	PMID:34177428;PMID:31595528	PCS		4/7			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0004719	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000238	PMID:34177428;PMID:31595528	PCS		2/7			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000873	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0031956	PMID:31595528	PCS		6/6			P	HPO:probinson[2022-01-23];HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003124	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000490	PMID:34177428;PMID:31595528	PCS		2/7			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002151	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0033614	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0100259	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0007430	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000007	PMID:31595528	PCS					I	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000369	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001612	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000126	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001396	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000582	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003577	PMID:31595528	PCS		4/6			C	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0010946	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000463	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001395	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001394	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002240	PMID:31595528	PCS		6/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0031964	PMID:31595528	PCS		5/6			P	HPO:probinson[2022-01-23];HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0040319	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0006695	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0025116	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001942	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0006579	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002410	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0006956	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001561	PMID:34177428;PMID:31595528	PCS		3/7			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000232	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001684	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002099	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0011622	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0010774	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002092	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0011344	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001159	PMID:34177428;PMID:31595528	PCS		2/7			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002007	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000589	PMID:34177428	PCS		0/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001651	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001250	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003155	PMID:31595528	PCS		5/6			P	HPO:probinson[2022-01-23];HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001252	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003270	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0011579	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001409	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001408	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000316	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003429	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002612	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001643	PMID:34177428;PMID:31595528	PCS		2/7			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002613	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000311	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000952	PMID:34177428;PMID:31595528	PCS		7/7			P	HPO:probinson[2022-01-23];HPO:probinson[2022-01-23];HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001541	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001382	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001263	PMID:31595528	PCS		4/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0011565	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0030948	PMID:31595528	PCS		6/6			P	HPO:probinson[2022-01-23];HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003281	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0031358	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0005180	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002908	PMID:31595528	PCS		6/6			P	HPO:probinson[2022-01-23];HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000969	PMID:34177428	PCS		0/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0012382	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0012383	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002904	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0012020	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0004927	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001659	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001257	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001655	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003774	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0010627	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000023	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0012408	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0033542	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002040	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0033149	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0010068	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0012766	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001508	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001629	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000938	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0006892	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000411	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0001744	PMID:31595528	PCS		4/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0004976	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0000276	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0005280	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0011304	PMID:31595528	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003811	PMID:31595528	PCS		1/6			C	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0002205	PMID:34177428	PCS		1/1			P	HPO:probinson[2022-01-23]
OMIM:619534	Biliary, renal, neurologic, and skeletal syndrome		HP:0003259	PMID:31595528	PCS		2/6			P	HPO:probinson[2022-01-23]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0003554	PMID:33772159	PCS		1/2			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002421	PMID:33772159;PMID:28540413	PCS		6/6			P	HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0003477	PMID:33772159;PMID:28540413	PCS		2/6			P	HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0010628	OMIM:617519	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0003577	PMID:33772159	PCS		2/5			C	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001250	OMIM:617519	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0003693	PMID:33772159	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0004463	PMID:33772159	PCS		1/2			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001252	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002020	PMID:33772159	PCS		3/3			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002460	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001290	PMID:33772159	PCS		5/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001270	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0034677	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0030319	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0040081	PMID:28540413	PCS		0/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0100704	OMIM:617519	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0007220	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0007002	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0000218	PMID:33772159;PMID:28540413	PCS		5/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0003623	PMID:33772159;PMID:28540413	PCS		4/6			C	HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0003700	PMID:33772159;PMID:28540413	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0007108	PMID:33772159	PCS		0/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0011807	PMID:33772159;PMID:28540413	PCS		3/3			P	HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002058	PMID:33772159;PMID:28540413	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002015	PMID:33772159	PCS		5/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002650	PMID:33772159;PMID:28540413	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002353	PMID:33772159	PCS		2/2			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001344	PMID:33772159	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001266	PMID:33772159	PCS		1/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0011968	PMID:33772159;PMID:28540413	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002033	PMID:33772159;PMID:28540413	PCS		6/6			P	HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0004891	PMID:33772159	PCS		5/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001263	OMIM:617519	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001284	PMID:33772159;PMID:28540413	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-03-31];HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002194	PMID:33772159	PCS		5/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0011344	PMID:28540413	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0011471	PMID:33772159	PCS	HP:0003593	4/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0000407	PMID:33772159	PCS		2/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0000007	PMID:33772159	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0001319	PMID:33772159	PCS	HP:0003623	5/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0006466	PMID:33772159	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0000666	PMID:33772159	PCS		2/5			P	HPO:probinson[2021-03-31]
OMIM:617519	Neurodevelopmental disorder with hypotonia, neuropathy, and deafness		HP:0002500	PMID:33772159	PCS		1/3			P	HPO:probinson[2021-03-31]
OMIM:229600	Fructose intolerance, hereditary		HP:0001254	OMIM:229600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229600	Fructose intolerance, hereditary		HP:0001397	OMIM:229600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229600	Fructose intolerance, hereditary		HP:0005973	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0001250	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0001394	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002240	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0003076	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0034830	PMID:213970	PCS					P	HPO:probinson[2023-07-18]
OMIM:229600	Fructose intolerance, hereditary		HP:0008273	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0001508	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0001943	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0003109	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002018	OMIM:229600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229600	Fructose intolerance, hereditary		HP:0003646	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0000114	OMIM:229600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002239	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002910	OMIM:229600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229600	Fructose intolerance, hereditary		HP:0000952	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0001942	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0003149	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0001249	OMIM:229600	TAS					P	HPO:skoehler[2013-06-16]
OMIM:229600	Fructose intolerance, hereditary		HP:0003128	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002013	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0004395	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002904	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0000007	OMIM:229600	IEA					I	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002027	OMIM:229600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229600	Fructose intolerance, hereditary		HP:0002049	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0002148	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:229600	Fructose intolerance, hereditary		HP:0001259	OMIM:229600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229600	Fructose intolerance, hereditary		HP:0002149	OMIM:229600	IEA					P	HPO:iea[2009-02-17]
OMIM:172870	Pigmented paravenous chorioretinal atrophy		HP:0007737	OMIM:172870	TAS					P	HPO:probinson[2009-02-17]
OMIM:172870	Pigmented paravenous chorioretinal atrophy		HP:0007903	OMIM:172870	TAS					P	HPO:probinson[2009-02-17]
OMIM:172870	Pigmented paravenous chorioretinal atrophy		HP:0000540	OMIM:172870	TAS					P	HPO:probinson[2009-02-17]
OMIM:172870	Pigmented paravenous chorioretinal atrophy		HP:0007773	OMIM:172870	TAS					P	HPO:probinson[2009-02-17]
OMIM:172870	Pigmented paravenous chorioretinal atrophy		HP:0001417	OMIM:172870	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:172870	Pigmented paravenous chorioretinal atrophy		HP:0000565	OMIM:172870	TAS					P	HPO:probinson[2009-02-17]
OMIM:172870	Pigmented paravenous chorioretinal atrophy		HP:0000006	OMIM:172870	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0000002	PMID:18784092	PCS		0/21			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-14]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0002079	OMIM:612475	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0001250	OMIM:612475	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0100753	OMIM:612475	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0000717	OMIM:612475	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0003829	OMIM:612475	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0000316	OMIM:612475	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0001328	OMIM:612475	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0003745	OMIM:612475	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0002007	OMIM:612475	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0000256	OMIM:612475	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612475	Chromosome 1q21.1 duplication syndrome		HP:0000006	OMIM:612475	IEA					I	HPO:skoehler[2010-06-19]
OMIM:148520	Keratosis palmaris et plantaris with clinodactyly		HP:0004209	OMIM:148520	IEA					P	HPO:iea[2009-02-17]
OMIM:148520	Keratosis palmaris et plantaris with clinodactyly		HP:0000006	OMIM:148520	IEA					I	HPO:iea[2009-02-17]
OMIM:148520	Keratosis palmaris et plantaris with clinodactyly		HP:0000951	OMIM:148520	IEA					P	HPO:iea[2009-02-17]
OMIM:157400	Milia, multiple eruptive		HP:0001056	OMIM:157400	TAS					P	HPO:probinson[2009-02-17]
OMIM:157400	Milia, multiple eruptive		HP:0000006	OMIM:157400	IEA					I	HPO:iea[2009-02-17]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0006429	OMIM:607078	TAS					P	HPO:probinson[2012-06-08]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0003365	OMIM:607078	TAS					P	HPO:probinson[2009-02-17]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0004322	PMID:14729835	PCS		3/7			P	HPO:probinson[2012-07-28];HPO:probinson[2021-02-26]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0003025	OMIM:607078	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0003088	OMIM:607078	TAS					P	HPO:probinson[2012-07-28]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0010049	PMID:15948199	PCS		1/1			P	HPO:probinson[2021-02-26]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0030838	PMID:15948199	PCS		1/1			P	HPO:probinson[2021-02-26]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0010585	OMIM:607078	TAS					P	HPO:probinson[2012-06-18]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0003090	OMIM:607078	TAS					P	HPO:probinson[2009-02-17]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0100864	PMID:15948199	PCS		1/1			P	HPO:probinson[2012-06-08];HPO:probinson[2021-02-26]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0002829	OMIM:607078	TAS					P	HPO:probinson[2009-02-17]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0010582	OMIM:607078	TAS					P	HPO:probinson[2012-06-18]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0008103	OMIM:607078	TAS					P	HPO:probinson[2009-02-17]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0002812	PMID:14729835	PCS		2/7			P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0002857	PMID:14729835	PCS		1/7			P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0002656	OMIM:607078	TAS					P	HPO:probinson[2009-02-17]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0002654	PMID:14729835	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0001216	OMIM:607078	TAS					P	HPO:probinson[2009-02-17]
OMIM:607078	Epiphyseal dysplasia, multiple, 5		HP:0000006	PMID:11479597	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:610504	Preterm premature rupture of the membranes		HP:0011462	PMID:16938879	PCS					C	HPO:probinson[2022-12-04]
OMIM:610504	Preterm premature rupture of the membranes		HP:0010982	PMID:16938879	PCS					I	HPO:skoehler[2013-02-28];HPO:probinson[2022-12-04]
OMIM:610504	Preterm premature rupture of the membranes		HP:0001788	PMID:16938879	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2022-12-04]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0002465	OMIM:618158	IEA					P	HPO:skoehler[2019-02-22]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0000750	PMID:30290153	PCS		2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0000276	PMID:30290153	PCS		2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0031936	OMIM:618158	IEA					P	HPO:skoehler[2019-02-22]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0001250	PMID:30290153	PCS		2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0002066	PMID:30290153	PCS		2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0000490	PMID:30290153	PCS		2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0001263	OMIM:618158	IEA					P	HPO:skoehler[2019-02-22]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0002020	PMID:30290153	PCS		1/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0030891	PMID:30290153	PCS		1/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0003593	OMIM:618158	IEA					C	HPO:skoehler[2019-02-22]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0010863	PMID:30290153	PCS		2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0012448	OMIM:618158	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0001290	OMIM:618158	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0001270	PMID:30290153	PCS	HP:0011463	2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0005490	OMIM:618158	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0008551	OMIM:618158	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0001988	PMID:30290153	PCS		1/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0020045	PMID:30290153	PCS		1/2			P	HP:probinson[2019-01-23];HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0000337	OMIM:618158	IEA					P	HPO:skoehler[2019-02-22]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0002317	OMIM:618158	IEA					P	HPO:skoehler[2019-02-22]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0002007	PMID:30290153	PCS		2/2			P	HP:probinson[2019-01-23]
OMIM:618158	Intellectual developmental disorder with macrocephaly, seizures, and speech delay		HP:0000006	PMID:30290153	PCS					I	HP:probinson[2019-01-23];HP:probinson[2019-01-23]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0002168	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0002300	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0002059	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0001250	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0001260	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0002063	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0001251	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0002361	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0000529	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0003819	OMIM:609055	IEA					C	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0001922	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0000007	OMIM:609055	IEA					I	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0000648	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0003208	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0002505	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0000510	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0001249	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0000654	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:609055	Ceroid lipofuscinosis, neuronal, 9		HP:0003205	OMIM:609055	IEA					P	HPO:iea[2009-02-17]
OMIM:612313	Glass syndrome		HP:0002069	PMID:17377962	PCS	HP:0025709	1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0004322	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0001250	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000160	OMIM:612313	TAS					P	HPO:skoehler[2014-11-26]
OMIM:612313	Glass syndrome		HP:0001252	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0003593	PMID:17377962	PCS		1/1			C	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0006390	PMID:17377962	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000319	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000718	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000711	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000678	PMID:24301056	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000752	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000358	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000677	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0001249	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000297	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000252	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000494	PMID:24301056	PCS		1/1			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000175	PMID:17377962;PMID:24301056	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0002033	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0001263	PMID:17377962	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0011800	OMIM:612313	TAS					P	HPO:skoehler[2013-11-28]
OMIM:612313	Glass syndrome		HP:0012385	OMIM:612313	TAS					P	HPO:skoehler[2013-10-22]
OMIM:612313	Glass syndrome		HP:0000527	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000201	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000963	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000369	PMID:24301056	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000006	PMID:17377962	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0002104	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0003577	PMID:24301056	PCS		1/1			C	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000343	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000023	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000463	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0002164	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000460	OMIM:612313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612313	Glass syndrome		HP:0040160	PMID:17377962	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0025161	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0008070	OMIM:612313	TAS					P	HPO:skoehler[2013-06-03]
OMIM:612313	Glass syndrome		HP:0040082	PMID:17377962	PCS		1/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000414	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000337	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000218	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000455	PMID:24301056	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000212	PMID:17377962	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000698	OMIM:612313	TAS					P	HPO:skoehler[2013-11-18]
OMIM:612313	Glass syndrome		HP:0001166	OMIM:612313	TAS					P	HPO:skoehler[2014-08-24]
OMIM:612313	Glass syndrome		HP:0002136	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0001762	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0003189	OMIM:612313	TAS					P	HPO:skoehler[2014-08-24]
OMIM:612313	Glass syndrome		HP:0000750	PMID:24301056	PCS		1/1			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000276	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0002373	PMID:17377962	PCS	HP:0011463	1/1			P	HPO:probinson[2022-11-06]
OMIM:612313	Glass syndrome		HP:0000272	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000426	OMIM:612313	TAS					P	HPO:skoehler[2014-08-24]
OMIM:612313	Glass syndrome		HP:0000348	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0002007	OMIM:612313	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612313	Glass syndrome		HP:0000347	PMID:17377962;PMID:24301056	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:153100	Lymphatic malformation 1		HP:0003577	PMID:15689446	PCS					C	HPO:iea[2009-02-17];HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0000034	PMID:15689446	PCS		13/35	MALE		P	HPO:iea[2009-02-17];HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0003550	PMID:15689446	PCS	HP:0003577	64/71			P	HPO:probinson[2009-02-17];HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0001790	PMID:16965327	PCS		HP:0040284			P	HPO:iea[2009-02-17];HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0032344	PMID:15689446	PCS		10/71			P	HP:probinson[2019-04-19]
OMIM:153100	Lymphatic malformation 1		HP:0012227	PMID:15689446	PCS		2/35			P	HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0012740	PMID:15689446	PCS		7/71			P	HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0100658	PMID:15689446	PCS		14/71			P	HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0003759	PMID:15689446	PCS		4/4			P	HPO:iea[2009-02-17];HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0001015	PMID:15689446	PCS		16/71			P	HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0000006	PMID:15689446	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-02-19]
OMIM:153100	Lymphatic malformation 1		HP:0007448	OMIM:153100	TAS					P	HPO:iea[2009-02-17]
OMIM:153100	Lymphatic malformation 1		HP:0001028	OMIM:153100	TAS					P	HPO:iea[2009-02-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0002110	OMIM:604571	TAS					P	HPO:skoehler[2010-06-20]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0002097	OMIM:604571	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0000007	OMIM:604571	TAS					I	HPO:skoehler[2009-02-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0100582	OMIM:604571	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0002837	OMIM:604571	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0001083	OMIM:604571	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0011109	OMIM:604571	TAS					P	HPO:skoehler[2010-06-20]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0000389	OMIM:604571	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0011950	OMIM:604571	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604571	Bare lymphocyte syndrome, type I		HP:0200042	OMIM:604571	TAS					P	HPO:skoehler[2010-06-20]
OMIM:247640	Lymphoblastic leukemia, acute, with lymphomatous features		HP:0006727	OMIM:247640	TAS					P	HPO:probinson[2009-02-17]
OMIM:247640	Lymphoblastic leukemia, acute, with lymphomatous features		HP:0000007	OMIM:247640	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:247640	Lymphoblastic leukemia, acute, with lymphomatous features		HP:0006721	OMIM:247640	TAS					P	HPO:probinson[2012-07-16]
OMIM:247640	Lymphoblastic leukemia, acute, with lymphomatous features		HP:0002665	OMIM:247640	TAS					P	HPO:probinson[2009-02-17]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0004754	PMID:27066836	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-10]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0001709	PMID:27066836	PCS		1/6			P	HPO:probinson[2022-07-10]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0001662	PMID:27066836	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-10]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0011705	PMID:27066836	PCS		3/6			P	HPO:probinson[2022-07-10]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0011462	PMID:27066836	PCS		5/5			C	HPO:probinson[2022-07-10]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0001962	PMID:27066836	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-10]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0004757	PMID:27066836	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-10]
OMIM:617280	Atrial fibrillation, familial, 18		HP:0000006	PMID:27066836	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-10]
OMIM:147820	Internal carotid artery, spontaneous dissection of		HP:0004945	OMIM:147820	IEA					P	HPO:iea[2009-02-17]
OMIM:147820	Internal carotid artery, spontaneous dissection of		HP:0000006	OMIM:147820	IEA					I	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0010628	OMIM:158900	TAS					P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0003236	OMIM:158900	TAS					P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0001250	OMIM:158900	IEA					P	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0003691	OMIM:158900	IEA					P	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:6001102	PMID:33113021	PCS					P	HPO:probinson[2024-12-14]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0012231	OMIM:158900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0012473	OMIM:158900	TAS					P	HPO:skoehler[2013-11-28]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0009023	OMIM:158900	IEA					P	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0011463	OMIM:158900	IEA					C	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0008970	OMIM:158900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0007763	OMIM:158900	TAS					P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0003547	OMIM:158900	TAS					P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0003724	OMIM:158900	TAS					P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0001249	OMIM:158900	IEA					P	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0003202	OMIM:158900	TAS					P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0002015	OMIM:158900	TAS		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:6001010	PMID:30804066	PCS					P	HPO:probinson[2024-08-04]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0030664	OMIM:158900	TAS					P	HPO:skoehler[2015-12-30]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:6000864	PMID:27922500	PCS					P	HPO:probinson[2024-08-03]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0002091	OMIM:158900	IEA					P	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0000407	OMIM:158900	TAS					P	HPO:probinson[2012-04-11]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0008981	OMIM:158900	IEA					P	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0000006	OMIM:158900	IEA					I	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0003677	OMIM:158900	IEA					C	HPO:iea[2009-02-17]
OMIM:158900	Facioscapulohumeral muscular dystrophy 1		HP:0000544	OMIM:158900	IEA					P	HPO:iea[2009-02-17]
OMIM:613958	Spermatogenic failure 9		HP:0003251	PMID:21397063	PCS		7/7			P	HPO:probinson[2022-03-10]
OMIM:613958	Spermatogenic failure 9		HP:0011462	PMID:21397063	PCS		7/7			C	HPO:probinson[2022-03-10]
OMIM:613958	Spermatogenic failure 9		HP:0000007	PMID:21397063	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-10]
OMIM:613958	Spermatogenic failure 9		HP:0012205	PMID:21397063	PCS		7/7			P	HPO:skoehler[2013-03-15];HPO:probinson[2022-03-10]
OMIM:115800	Cataract, crystalline coralliform		HP:0000518	OMIM:115800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:115800	Cataract, crystalline coralliform		HP:0000006	OMIM:115800	IEA					I	HPO:iea[2009-02-17]
OMIM:613780	Aortic aneurysm, familial thoracic 7		HP:0031649	PMID:27586135	PCS		2/5			P	HPO:probinson[2021-05-23]
OMIM:613780	Aortic aneurysm, familial thoracic 7		HP:0012499	PMID:21055718	PCS	HP:0003581	2/17			P	HPO:probinson[2021-05-23]
OMIM:613780	Aortic aneurysm, familial thoracic 7		HP:0004933	PMID:21055718	PCS	HP:0003581	7/17			P	HPO:probinson[2021-05-23]
OMIM:613780	Aortic aneurysm, familial thoracic 7		HP:0004933	PMID:27586135	PCS		3/5			P	HPO:probinson[2021-05-23]
OMIM:613780	Aortic aneurysm, familial thoracic 7		HP:0000006	PMID:21055718	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23]
OMIM:613780	Aortic aneurysm, familial thoracic 7		HP:0004942	PMID:21055718	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23]
OMIM:613780	Aortic aneurysm, familial thoracic 7		HP:0001699	PMID:21055718	PCS		1/17			P	HPO:probinson[2021-05-23]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000164	PMID:20617341	PCS		0/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0003621	PMID:20617341	PCS		5/5			C	HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000485	PMID:20617341	PCS		0/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000540	OMIM:251750	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0030961	PMID:20617341	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0001083	PMID:20617341	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0100693	OMIM:251750	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000767	OMIM:251750	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000007	PMID:20617341	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000557	PMID:20617341	PCS		0/5			P	HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000218	OMIM:251750	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0007765	OMIM:251750	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000501	PMID:20617341	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-10]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000545	OMIM:251750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251750	Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma		HP:0000951	PMID:20617341	PCS		0/5			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-04-10]
OMIM:613794	Retinitis pigmentosa 20		HP:0000662	PMID:9326941	PCS					P	HPO:probinson[2013-06-05];HPO:probinson[2022-11-11]
OMIM:613794	Retinitis pigmentosa 20		HP:0000639	PMID:9326941	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:613794	Retinitis pigmentosa 20		HP:0011463	PMID:9326941	PCS					C	HPO:probinson[2022-11-11]
OMIM:613794	Retinitis pigmentosa 20		HP:0001141	PMID:9326941	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:613794	Retinitis pigmentosa 20		HP:0000007	PMID:9326941	PCS					I	HPO:probinson[2013-06-05];HPO:probinson[2022-11-11]
OMIM:613794	Retinitis pigmentosa 20		HP:0000505	PMID:9326941	PCS					P	HPO:probinson[2013-06-05];HPO:probinson[2022-11-11]
OMIM:613794	Retinitis pigmentosa 20		HP:0000510	PMID:9326941	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-11-11]
OMIM:613794	Retinitis pigmentosa 20		HP:0007843	PMID:9326941	PCS					P	HPO:probinson[2013-06-05];HPO:probinson[2022-11-11]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0000252	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0003563	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0003233	PMID:21285510	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0002750	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0003146	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0004322	PMID:21285510	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0001263	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:6001113	OMIM:616834	TAS					P	HPO:probinson[2024-12-14]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:6000753	PMID:21285510	PCS		1/1			P	HPO:probinson[2024-06-29]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:6000754	PMID:21285510	PCS		1/1			P	HPO:probinson[2024-06-29]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0008064	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0001508	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0002829	OMIM:616834	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0011463	PMID:21285510	PCS		1/1			C	HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0000519	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0000007	PMID:21285510	PCS					I	HPO:probinson[2017-06-17]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0000823	OMIM:616834	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0000498	PMID:21285510	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-08]
OMIM:616834	Microcephaly, congenital cataract, and psoriasiform dermatitis		HP:0003765	PMID:21285510	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-03-08]
OMIM:601390	Van Maldergem syndrome 1		HP:0000286	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0010804	OMIM:601390	TAS					P	HPO:skoehler[2014-11-26]
OMIM:601390	Van Maldergem syndrome 1		HP:0002023	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000089	PMID:24056717	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0001252	PMID:22473091	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0001290	OMIM:601390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601390	Van Maldergem syndrome 1		HP:0012745	OMIM:601390	TAS					P	HPO:skoehler[2014-03-24]
OMIM:601390	Van Maldergem syndrome 1		HP:0000316	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0002779	PMID:22473091	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0001249	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0003048	PMID:22473091	PCS		3/4			P	HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0002079	PMID:22473091	PCS		2/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0032409	OMIM:601390	IEA					P	HPO:skoehler[2019-04-18]
OMIM:601390	Van Maldergem syndrome 1		HP:0011968	PMID:22473091	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0001382	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0001263	PMID:22473091	PCS		3/3			P	HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0010554	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0011800	OMIM:601390	TAS					P	HPO:skoehler[2015-11-15]
OMIM:601390	Van Maldergem syndrome 1		HP:0012385	PMID:22473091	PCS		4/4			P	HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0000407	PMID:24056717	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0010044	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000327	PMID:22473091	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0000007	PMID:24056717	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0000689	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000405	PMID:22473091	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0000047	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000960	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0004689	OMIM:601390	TAS					P	HPO:skoehler[2014-02-06]
OMIM:601390	Van Maldergem syndrome 1		HP:0000341	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0003577	PMID:22473091	PCS		4/4			C	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0000260	PMID:22473091	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0000581	PMID:22473091	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0002282	OMIM:601390	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601390	Van Maldergem syndrome 1		HP:0040079	OMIM:601390	TAS					P	HPO:skoehler[2014-11-26]
OMIM:601390	Van Maldergem syndrome 1		HP:0000938	PMID:22473091	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0008551	PMID:22473091	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0030084	OMIM:601390	TAS					P	HPO:skoehler[2014-09-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0002714	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000218	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000774	PMID:22473091	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0001302	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000894	PMID:22473091	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0000413	OMIM:601390	TAS					P	HPO:skoehler[2014-02-06]
OMIM:601390	Van Maldergem syndrome 1		HP:0001545	PMID:22473091	PCS		1/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0001760	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0002652	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0002650	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0001762	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000431	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000272	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0032388	PMID:24056717	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0010537	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000508	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0001510	OMIM:601390	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601390	Van Maldergem syndrome 1		HP:0000347	PMID:22473091	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-21]
OMIM:601390	Van Maldergem syndrome 1		HP:0009879	OMIM:601390	TAS					P	HPO:skoehler[2014-11-26]
OMIM:311360	Premature ovarian failure 1		HP:0008209	PMID:10528856	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:311360	Premature ovarian failure 1		HP:0000837	OMIM:311360	IEA					P	HPO:iea[2009-02-17]
OMIM:311360	Premature ovarian failure 1		HP:0000858	OMIM:311360	IEA					P	HPO:iea[2009-02-17]
OMIM:311360	Premature ovarian failure 1		HP:0003581	PMID:10528856	PCS					C	HPO:probinson[2022-08-04]
OMIM:311360	Premature ovarian failure 1		HP:0001417	PMID:10528856	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0003577	PMID:27889062	PCS					C	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0004334	PMID:27889062	PCS		14/14			P	HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0001596	PMID:27889062	PCS		7/14			P	HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0002231	OMIM:617294	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0008066	PMID:27798626	PCS		5/5			P	HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0008066	PMID:27889062	PCS	HP:0003577	14/14			P	HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0001010	PMID:27889062	PCS		14/14			P	HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0002293	PMID:27798626	PCS	HP:0011462	1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0008401	PMID:27889062	PCS		8/14			P	HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0007447	PMID:27889062;PMID:27798626	PCS		15/15			P	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0000006	PMID:27798626	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-02]
OMIM:617294	Epidermolysis bullosa simplex, generalized, with scarring and hair loss		HP:0001810	PMID:27798626	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-02]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0002257	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0001696	PMID:33389130	PCS		1/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0002110	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0003251	PMID:33389130	PCS	HP:0011462	3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0033036	PMID:33389130	PCS		1/2			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0012207	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0031245	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0011108	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0032558	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0032559	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0033393	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0034011	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0011463	PMID:33389130	PCS		3/3			C	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0000007	PMID:33389130	PCS					I	HPO:probinson[2024-02-15];HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0002205	PMID:33389130	PCS		3/3			P	HPO:probinson[2024-02-15]
OMIM:620438	Ciliary dyskinesia, primary, 51		HP:0000798	PMID:33389130	PCS		2/3			P	HPO:probinson[2024-02-15]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000341	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000244	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0004322	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0002021	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0001250	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0001274	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000085	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0001290	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0002280	OMIM:218350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0011217	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0001629	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000238	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0002119	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0001643	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0003745	OMIM:218350	TAS					I	HPO:skoehler[2015-12-30]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0001249	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000357	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0002079	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000272	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0011800	OMIM:218350	TAS				HP:0012825	P	HPO:skoehler[2013-11-28]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0007099	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000348	OMIM:218350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000565	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0002007	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000047	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000028	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:218350	Craniofacial dyssynostosis with short stature		HP:0000248	OMIM:218350	TAS					P	HPO:skoehler[2012-10-14]
OMIM:614945	Deafness, autosomal recessive 18B		HP:0003577	PMID:23122587	PCS		6/6			C	HPO:probinson[2023-02-12]
OMIM:614945	Deafness, autosomal recessive 18B		HP:0000750	PMID:23122587	PCS		3/6			P	HPO:probinson[2023-02-12]
OMIM:614945	Deafness, autosomal recessive 18B		HP:0000407	PMID:23122587	PCS		6/6			P	HPO:probinson[2023-02-12]
OMIM:614945	Deafness, autosomal recessive 18B		HP:0000007	PMID:23122587	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2023-02-12]
OMIM:614945	Deafness, autosomal recessive 18B		HP:0001756	PMID:23122587	PCS		4/6			P	HPO:probinson[2023-02-12]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0003676	PMID:23913003	PCS					C	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0003596	PMID:23913003	PCS		3/16			C	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002321	PMID:23913003	PCS		4/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0025041	PMID:23913003	PCS		7/31			P	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0100034	PMID:23913003	PCS		1/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0033051	PMID:23913003	PCS		5/31			P	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0100543	PMID:23913003	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0000716	PMID:23913003	PCS		4/31			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0011463	PMID:23913003	PCS		2/16			C	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0011462	PMID:23913003	PCS		5/16			C	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0000739	PMID:23913003	PCS		2/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002514	PMID:23913003	PCS		12/31			P	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002135	PMID:23913003	PCS		31/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002378	PMID:23913003	PCS		1/31			P	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0003621	PMID:23913003	PCS		6/16			C	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0001300	PMID:23913003	PCS		3/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002354	PMID:23913003	PCS		4/31			P	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002076	PMID:23913003	PCS		7/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0001260	PMID:23913003	PCS		1/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002174	PMID:23913003	PCS		2/31			P	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002072	PMID:23913003	PCS		2/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0100660	PMID:23913003	PCS		5/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0000709	PMID:23913003	PCS		3/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0000726	PMID:23913003	PCS		1/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0007352	PMID:23913003	PCS		11/31			P	HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0000741	PMID:23913003	PCS		1/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0002305	PMID:23913003	PCS		1/31			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:615483	Basal ganglia calcification, idiopathic, 5		HP:0000006	PMID:23913003	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-06-06]
OMIM:619291	Dystonia 30		HP:0000473	PMID:32808683	PCS		5/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0002356	PMID:32808683	PCS		3/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0002444	PMID:32808683	PCS		1/16			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0003621	PMID:32808683	PCS		11/18			C	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0003596	PMID:32808683	PCS		1/18			C	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0001332	PMID:32808683	PCS		19/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0031959	PMID:32808683	PCS		3/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0001250	PMID:32808683	PCS		2/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0031960	PMID:32808683	PCS		3/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0033049	PMID:32808683	PCS		4/16			P	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0012048	PMID:32808683	PCS		3/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0100710	PMID:32808683	PCS		2/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0011463	PMID:32808683	PCS		2/18			C	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0000718	PMID:32808683	PCS		1/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0011462	PMID:32808683	PCS		4/18			C	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0002506	PMID:32808683	PCS		4/19		HP:0012825	P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0000722	PMID:32808683	PCS		1/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0007302	PMID:32808683	PCS		1/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0002505	PMID:32808683	PCS		3/19			P	HPO:probinson[2021-05-29]
OMIM:619291	Dystonia 30		HP:0000006	PMID:32808683	PCS					I	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:300245	Ptosis, hereditary congenital 2		HP:0000508	OMIM:300245	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300245	Ptosis, hereditary congenital 2		HP:0001423	OMIM:300245	TAS					I	HPO:skoehler[2013-05-29]
OMIM:300245	Ptosis, hereditary congenital 2		HP:0001477	OMIM:300245	IEA					P	HPO:skoehler[2010-06-19]
OMIM:250300	Metaphyseal chondrodysplasia, Pena type		HP:0005871	OMIM:250300	TAS					P	HPO:probinson[2009-02-17]
OMIM:250300	Metaphyseal chondrodysplasia, Pena type		HP:0001939	OMIM:250300	IEA					P	HPO:iea[2009-02-17]
OMIM:250300	Metaphyseal chondrodysplasia, Pena type		HP:0000007	OMIM:250300	IEA					I	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0004401	OMIM:219700	IEA					P	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0006528	OMIM:219700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219700	Cystic fibrosis		HP:0003251	OMIM:219700	IEA					P	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0002240	PMID:30558651	PCS		1/71			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0001394	PMID:30558651	PCS		2/71			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0003593	PMID:10777364	PCS		6/7			C	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0032359	PMID:26826884	PCS		15/21			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0001508	PMID:26826884	PCS		8/21			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0011463	PMID:10777364	PCS		1/7			C	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0032341	PMID:26826884	PCS		5/21			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0032342	PMID:26826884;PMID:32539862	PCS		26/39			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0001944	OMIM:219700	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0001648	PMID:10777364	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0006532	PMID:26826884	PCS		8/21			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0002613	OMIM:219700	IEA					P	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0002014	PMID:30558651	PCS		15/71			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0006538	OMIM:219700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219700	Cystic fibrosis		HP:0002595	PMID:30558651	PCS		3/71			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0002035	OMIM:219700	IEA					P	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0002099	OMIM:219700	IEA					P	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0002110	PMID:26826884;PMID:32539862;PMID:30558651	PCS		106/111			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-23];HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:6000100	PMID:21594779	PCS					P	HPO:probinson[2024-01-06]
OMIM:219700	Cystic fibrosis		HP:0002570	PMID:26826884	PCS		3/21			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0002150	OMIM:219700	IEA					P	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0100582	PMID:26826884	PCS		1/21			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0011109	PMID:26826884;PMID:32539862;PMID:30558651	PCS		59/112			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0012236	PMID:10777364;PMID:32539862;PMID:30558651	PCS		77/77			P	HPO:probinson[2021-02-23];HPO:probinson[2013-03-31];HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:6000725	PMID:25640976	PCS		21/49			P	HPO:probinson[2024-06-29]
OMIM:219700	Cystic fibrosis		HP:0001738	PMID:10777364;PMID:32539862	PCS		11/27			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-23];HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0100759	PMID:26826884	PCS		9/21			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0000007	OMIM:219700	IEA					I	HPO:iea[2009-02-17]
OMIM:219700	Cystic fibrosis		HP:0001433	PMID:30558651	PCS		2/71			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0001733	PMID:26826884	PCS		2/21			P	HPO:probinson[2021-02-23]
OMIM:219700	Cystic fibrosis		HP:0002105	PMID:26826884	PCS		3/21			P	HPO:probinson[2021-02-23]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002583	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0025343	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0011850	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0000316	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0000952	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001369	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0005404	PMID:36932076	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0003623	PMID:36932076;PMID:36122175	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0003565	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0031956	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001025	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0004970	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0025379	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0030783	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0030948	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0012378	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002908	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:4000037	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002829	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0100539	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002027	PMID:36932076;PMID:36122175	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001974	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001396	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001395	PMID:36932076	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002240	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0010783	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0031964	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001508	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001903	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0000979	PMID:36932076	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0100828	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001789	PMID:36932076	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001945	PMID:36932076;PMID:36122175	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002315	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001744	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001622	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0006559	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002014	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002850	PMID:36932076	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001047	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001640	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0000155	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0410242	PMID:36932076	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002099	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0030167	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0000031	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0011944	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0011227	PMID:36932076;PMID:36122175	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0033040	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0000509	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002923	PMID:36932076	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001511	PMID:36932076;PMID:36122175	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002007	PMID:36122175	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001433	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0001873	PMID:36932076	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620376	Autoinflammatory disease, systemic, with vasculitis		HP:0002720	PMID:36932076	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000341	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002169	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0003577	OMIM:300523	TAS					C	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002188	OMIM:300523	TAS					P	HPO:skoehler[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002540	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001371	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001251	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000737	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001822	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0008872	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001763	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002415	OMIM:300523	IEA					P	HPO:skoehler[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001347	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0003700	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000252	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000395	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002510	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001583	OMIM:300523	TAS		HP:0040283			P	HPO:probinson[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002650	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0003487	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001260	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0011344	OMIM:300523	TAS					P	HPO:skoehler[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0100015	OMIM:300523	IEA					P	HPO:skoehler[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0008583	PMID:15488219	PCS					P	HPO:probinson[2016-07-25]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001419	PMID:15980113	PCS					I	HPO:probinson[2020-07-19]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000767	PMID:15488219	PCS					P	HPO:skoehler[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000821	OMIM:300523	IEA					P	HPO:skoehler[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002925	OMIM:300523	TAS				HP:0012825	P	HPO:skoehler[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000549	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001319	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002307	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0000400	OMIM:300523	IEA					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0001258	OMIM:300523	TAS					P	HPO:iea[2018-03-07]
OMIM:300523	Allan-Herndon-Dudley syndrome		HP:0002305	PMID:15488219	PCS					P	HPO:probinson[2016-07-25]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0004325	PMID:37943617	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0003577	PMID:37943617	PCS		5/5			C	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0004322	PMID:37943617	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0001250	PMID:37943617	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002120	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0001251	PMID:37943617	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0012469	PMID:37943617	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0001629	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000817	PMID:37943617	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0100806	PMID:37943617	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000778	PMID:37943617	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002878	PMID:37943617	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000219	PMID:37943617	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0008936	PMID:37943617	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000054	PMID:37943617	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000252	PMID:37943617	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0001344	PMID:37943617	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002232	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0004432	PMID:37943617	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002299	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000293	PMID:37943617	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002352	PMID:37943617	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002572	PMID:37943617	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0001263	PMID:37943617	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0012416	PMID:37943617	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002092	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0011400	PMID:37943617	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0002093	PMID:37943617	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0011344	PMID:37943617	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0011787	PMID:37943617	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0001919	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000508	PMID:37943617	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0001999	PMID:37943617	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000767	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000821	PMID:37943617	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000307	PMID:37943617	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000648	PMID:37943617	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000400	PMID:37943617	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0008404	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000501	PMID:37943617	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:621068	Neurodevelopmental disorder with hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia		HP:0000006	PMID:37943617	PCS					I	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:254600	Myeloperoxidase deficiency		HP:0001871	OMIM:254600	IEA					P	HPO:iea[2009-02-17]
OMIM:254600	Myeloperoxidase deficiency		HP:0001939	OMIM:254600	IEA					P	HPO:iea[2009-02-17]
OMIM:254600	Myeloperoxidase deficiency		HP:6000375	OMIM:254600	TAS					P	HPO:probinson[2024-02-27]
OMIM:254600	Myeloperoxidase deficiency		HP:0002715	OMIM:254600	IEA					P	HPO:iea[2009-02-17]
OMIM:254600	Myeloperoxidase deficiency		HP:6000513	PMID:9354683	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:254600	Myeloperoxidase deficiency		HP:0000007	OMIM:254600	IEA					I	HPO:iea[2009-02-17]
OMIM:167500	Palatopharyngeal incompetence		HP:0000220	OMIM:167500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:167500	Palatopharyngeal incompetence		HP:0000175	OMIM:167500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:167500	Palatopharyngeal incompetence		HP:0001608	OMIM:167500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:167500	Palatopharyngeal incompetence		HP:0001426	OMIM:167500	TAS					I	HPO:skoehler[2009-02-17]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000343	PMID:32109419	PCS		1/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000684	PMID:32109419	PCS		0/8			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000463	PMID:32109419	PCS		1/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0001250	PMID:32109419	PCS		3/9			P	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0003593	PMID:32109419	PCS		9/9			C	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0008770	PMID:32109419	PCS		4/8			P	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0007021	PMID:32109419	PCS		1/8			P	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000718	PMID:32109419	IEA		3/9			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0012450	PMID:32109419	PCS		2/9			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000316	PMID:32109419	PCS		1/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000733	PMID:32109419	PCS		4/9			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0008872	PMID:32109419	PCS		5/8			P	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000678	PMID:32109419	PCS		1/8			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0009765	PMID:32109419	PCS		2/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000218	PMID:32109419	PCS		1/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0025336	PMID:32109419	IEA		2/9			P	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000256	PMID:32109419	PCS		7/9			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0001249	PMID:32109419	PCS		9/9			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000154	PMID:32109419	PCS		2/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0002553	PMID:32109419	PCS		2/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000494	PMID:32109419	PCS		1/7			P	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000750	PMID:32109419	PCS		9/9			P	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0002650	PMID:32109419	PCS		4/8			P	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000430	PMID:32109419	PCS		1/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000331	PMID:32109419	PCS		1/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0031936	PMID:32109419	PCS		9/9			P	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0001263	PMID:32109419	PCS					P	HPO:probinson[2020-05-12]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0001182	PMID:32109419	PCS		2/8			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000426	PMID:32109419	PCS		1/7			P	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0002007	PMID:32109419	PCS		5/7			P	HPO:probinson[2020-05-12];HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0007018	PMID:32109419	PCS		4/9			P	HPO:probinson[2022-04-02]
OMIM:618825	Intellectual developmental disorder, autosomal dominant 63, with macrocephaly		HP:0000006	PMID:32109419	PCS					I	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0002069	PMID:24272827	PCS		1/1			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0000252	PMID:20890276	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0002133	PMID:24272827	PCS		1/1			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0002353	PMID:20890276	PCS		3/6			P	HPO:probinson[2013-08-10];HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0000453	PMID:20890276	PCS		1/6			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0000023	PMID:20890276	PCS		1/6			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0001332	OMIM:613970	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0001250	PMID:20890276	PCS		0/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0002384	PMID:24272827	PCS		1/1			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0001263	PMID:24272827	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0001290	OMIM:613970	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0002072	OMIM:613970	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0100660	OMIM:613970	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0000708	PMID:20890276	PCS		6/6			P	HPO:probinson[2013-08-10];HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0000821	PMID:20890276	PCS		1/6			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0001257	OMIM:613970	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0001763	PMID:20890276	PCS		1/6			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0001249	PMID:20890276;PMID:24272827	PCS		7/7			P	HPO:probinson[2013-08-10];HPO:probinson[2022-06-16];HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0000028	PMID:20890276	PCS		1/4			P	HPO:probinson[2022-06-16]
OMIM:613970	Intellectual developmental disorder, autosomal dominant 6, with or without seizures		HP:0000006	PMID:20890276	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-06-16]
OMIM:115196	Cardiomyopathy, familial hypertrophic, 3		HP:0001639	PMID:11136687	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:115196	Cardiomyopathy, familial hypertrophic, 3		HP:0000006	PMID:8205619	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:115196	Cardiomyopathy, familial hypertrophic, 3		HP:0001645	PMID:11136687	PCS		13/26			P	HPO:probinson[2022-07-10]
OMIM:163000	Nevi flammei, familial multiple		HP:0001052	OMIM:163000	IEA					P	HPO:skoehler[2009-02-17]
OMIM:163000	Nevi flammei, familial multiple		HP:0000006	OMIM:163000	IEA					I	HPO:iea[2009-02-17]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0000572	PMID:30967659	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0003621	PMID:30967659	PCS					C	HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0000970	PMID:30967659	PCS		13/13			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0001025	PMID:30967659	PCS		1/15			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0002076	PMID:30967659	PCS		6/14			P	HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0001954	PMID:30967659	PCS		2/15			P	HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0000548	PMID:30967659	PCS		6/15			P	HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0000006	PMID:30967659	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0001876	PMID:30967659	PCS		12/14		HP:0012825	P	HPO:skoehler[2015-08-16];HPO:probinson[2022-09-30]
OMIM:614979	Splenomegaly, cytopenia, and vision loss		HP:0001744	PMID:30967659	PCS		12/14			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-30]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0001276	PMID:32142645	PCS		5/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0002135	PMID:32142645	PCS		7/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0001300	PMID:32142645	PCS		5/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0002067	PMID:32142645	PCS		5/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0003487	PMID:32142645	PCS		5/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0002310	PMID:32142645	PCS		2/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0001250	PMID:32142645	PCS		1/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0001260	PMID:32142645	PCS		3/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0002451	PMID:32142645	PCS		2/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0002063	PMID:32142645	PCS		3/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0002070	PMID:32142645	PCS		6/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0025041	PMID:32142645	PCS		5/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0000639	PMID:32142645	PCS		2/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0000729	PMID:32142645	PCS		1/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0007352	PMID:32142645	PCS		6/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0000338	PMID:32142645	PCS		2/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0000007	PMID:32142645	PCS					I	HPO:probinson[2020-05-12];HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0007325	PMID:32142645	PCS		1/7			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0001268	PMID:32142645	PCS		4/6			P	HPO:probinson[2020-05-12]
OMIM:618824	Basal ganglia calcification, idiopathic, 8, autosomal recessive		HP:0001348	PMID:32142645	PCS		5/7			P	HPO:probinson[2020-05-12]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000341	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0004742	PMID:26293662	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0003577	PMID:26293662	PCS		2/2			C	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0003236	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001770	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0006528	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000463	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000023	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001250	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0003155	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0003273	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0010943	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0010844	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0100704	PMID:26293662	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000718	OMIM:616809	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000938	PMID:26293662	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000519	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0004719	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000218	PMID:26293662	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001522	PMID:26293662	PCS		1/2			C	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0009748	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0006118	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0008936	PMID:26293662	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001385	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0009826	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001561	PMID:26293662	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0002376	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0002013	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0011968	PMID:26293662	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000490	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001263	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000470	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0004691	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001181	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0005280	PMID:26293662	PCS		2/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0006380	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0003819	PMID:26293662	PCS		1/2			C	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0033165	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0009894	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000007	PMID:26293662	PCS					I	HPO:probinson[2017-06-18]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0000505	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0004209	PMID:26293662	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0002987	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0001510	PMID:26293662	PCS		1/2			P	HPO:probinson[2017-06-18];HPO:probinson[2022-08-27]
OMIM:616809	Hyperphosphatasia with impaired intellectual development syndrome 6		HP:0002027	PMID:26293662	TAS		2/2			P	HPO:nvasilevsky[2019-03-27];HPO:nvasilevsky[2019-03-27];HPO:probinson[2022-08-27]
OMIM:608389	Branchiootic syndrome 3		HP:0004467	PMID:10762556	PCS					P	HPO:probinson[2013-03-24]
OMIM:608389	Branchiootic syndrome 3		HP:0000384	OMIM:608389	TAS					P	HPO:skoehler[2015-09-11]
OMIM:608389	Branchiootic syndrome 3		HP:0000407	PMID:10762556	PCS					P	HPO:probinson[2013-03-24]
OMIM:608389	Branchiootic syndrome 3		HP:0009796	OMIM:608389	TAS					P	HPO:skoehler[2015-10-09]
OMIM:608389	Branchiootic syndrome 3		HP:0007678	OMIM:608389	TAS					P	HPO:skoehler[2015-09-11]
OMIM:608389	Branchiootic syndrome 3		HP:0000006	PMID:10762556	PCS					I	HPO:probinson[2013-01-09]
OMIM:608389	Branchiootic syndrome 3		HP:0002710	PMID:10762556	PCS					P	HPO:probinson[2013-03-24]
OMIM:216340	Yunis-Varon syndrome		HP:0000242	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000882	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0006628	PMID:23623387	PCS		9/12			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002021	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0000518	OMIM:216340	IEA					P	HPO:iea[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0000239	PMID:20932945;PMID:23623387	PCS		22/25			P	HPO:probinson[2022-01-22];HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002139	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0200021	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0004611	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000252	PMID:8411078;PMID:23623387	PCS		13/25			P	HPO:probinson[2022-01-22];HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0004331	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0001182	PMID:20932945	PCS		2/2			P	HPO:probinson[2013-04-09];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0008362	PMID:8411078	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000407	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002827	PMID:23623387	PCS		6/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0009576	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000007	PMID:23623387	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000647	OMIM:216340	IEA					P	HPO:iea[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0000520	PMID:8411078;PMID:23623387	PCS		17/21			P	HPO:probinson[2022-01-22];HPO:skoehler[2013-07-30];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000369	PMID:8411078;PMID:23623387	PCS		27/27			P	HPO:probinson[2022-01-22];HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000187	OMIM:216340	TAS					P	HPO:probinson[2022-02-01]
OMIM:216340	Yunis-Varon syndrome		HP:0003577	PMID:8411078;PMID:20932945	PCS		3/3			C	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000582	PMID:8411078	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000463	PMID:23623387	PCS		16/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000188	PMID:23623387	PCS		20/21			P	HPO:skoehler[2013-07-30];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001274	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0005474	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0012725	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000737	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0009565	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001789	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0009843	PMID:23623387	PCS		16/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000219	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0030084	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000218	PMID:20932945;PMID:23623387	PCS		15/19			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001302	PMID:20932945;PMID:23623387	PCS		3/10			P	HPO:probinson[2022-01-22];HPO:skoehler[2013-07-30];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000972	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0005989	PMID:8411078;PMID:20932945;PMID:23623387	PCS		14/17			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001320	PMID:20932945	PCS		2/2			P	HPO:probinson[2022-01-22];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001561	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0000233	PMID:8411078	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001321	OMIM:216340	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:216340	Yunis-Varon syndrome		HP:0002092	OMIM:216340	TAS					P	HPO:skoehler[2013-05-29]
OMIM:216340	Yunis-Varon syndrome		HP:0011344	PMID:20932945	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0010537	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0003180	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002808	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0006323	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0000347	PMID:8411078;PMID:20932945;PMID:23623387	PCS		23/25			P	HPO:probinson[2022-01-22];HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001798	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0009835	PMID:23623387	PCS		19/21			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001831	PMID:20932945;PMID:23623387	PCS		25/26			P	HPO:probinson[2022-01-22];HPO:probinson[2012-06-09];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000286	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001374	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001770	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0001531	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001252	PMID:8411078;PMID:20932945;PMID:23623387	PCS		14/15			P	HPO:probinson[2022-01-22];HPO:skoehler[2014-11-26];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0045075	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0009381	PMID:23623387	PCS		21/23			P	HPO:probinson[2013-04-09];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000316	PMID:20932945	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000954	PMID:23623387	PCS		10/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001525	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0005469	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000054	OMIM:216340	IEA					P	HPO:iea[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0030148	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002079	PMID:20932945	PCS		2/2			P	HPO:probinson[2022-01-22];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0003561	PMID:23623387	PCS		10/22			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0011968	PMID:8411078;PMID:20932945	PCS		2/2			P	HPO:probinson[2022-01-22];HPO:probinson[2022-01-22];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001263	PMID:20932945	PCS		1/1			P	HPO:probinson[2022-01-22];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0005461	PMID:23623387	PCS		12/15			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0012386	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001817	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0006660	PMID:20932945;PMID:23623387	PCS		21/26			P	HPO:probinson[2022-01-22];HPO:skoehler[2013-10-22];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0009777	PMID:20932945;PMID:23623387	PCS		12/12			P	HPO:probinson[2022-01-22];HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0007598	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000047	OMIM:216340	IEA					P	HPO:iea[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0009536	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000322	PMID:23623387	PCS		9/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0009778	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001655	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000385	OMIM:216340	IEA					P	HPO:iea[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0002683	PMID:23623387	PCS		19/21			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001871	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0002561	PMID:23623387	PCS		4/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0011951	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0010743	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001629	PMID:20932945	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0008551	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0009882	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000378	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002557	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000411	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000653	PMID:20932945	PCS		1/2			P	HPO:probinson[2012-03-01];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000894	PMID:20932945	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001622	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0025430	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000395	PMID:20932945	PCS		1/2			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0011309	PMID:20932945	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002692	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0001518	PMID:23623387	PCS		10/25			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0008386	PMID:23623387	PCS		22/24			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0008785	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0002209	PMID:8411078;PMID:20932945;PMID:23623387	PCS		26/27			P	HPO:probinson[2022-01-22];HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001636	PMID:8411078	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0007333	PMID:20932945	PCS		2/2			P	HPO:probinson[2022-01-22];HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0001638	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0000268	OMIM:216340	IEA					P	HPO:iea[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0001511	OMIM:216340	IEA					P	HPO:probinson[2009-02-17]
OMIM:216340	Yunis-Varon syndrome		HP:0001510	PMID:8411078	PCS		1/1			P	HPO:probinson[2022-01-22]
OMIM:216340	Yunis-Varon syndrome		HP:0000028	OMIM:216340	IEA					P	HPO:iea[2009-02-17]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001297	PMID:7493025	PCS		1/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-04]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001695	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0003198	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0002240	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0011712	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0030718	PMID:16679492	PCS		1/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0011713	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0012664	PMID:16679492	PCS		1/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0100749	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001645	PMID:7493025;PMID:9562578	PCS		35/293			P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0003623	PMID:16679492	PCS		2/2			C	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0031318	PMID:16679492	PCS		2/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0003621	PMID:9562578	PCS		8/121			C	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001663	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001640	PMID:16679492	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001541	PMID:16679492	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0002098	PMID:16679492	PCS		2/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0011705	PMID:16679492	PCS		1/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0005144	PMID:16679492	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0003581	PMID:9562578	PCS		113/121			C	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0002094	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0011623	PMID:16679492	PCS		1/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0100598	PMID:16679492	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001639	PMID:7493025	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-04]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001639	PMID:9562578	PCS	HP:0003596	68/117			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001639	PMID:16679492	PCS		2/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001635	PMID:16679492	PCS		2/2			P	HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0000007	PMID:16679492	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001714	PMID:9562578	PCS	HP:0003596	68/117			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-10]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0002326	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001698	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001279	PMID:7493025	PCS		1/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-07-04]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0000006	PMID:7493025	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-04]
OMIM:115197	Cardiomyopathy, familial hypertrophic, 4		HP:0001678	OMIM:115197	IEA					P	HPO:skoehler[2019-09-07]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0002069	OMIM:249650	TAS					P	HPO:skoehler[2010-06-18]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0002375	OMIM:249650	TAS					P	HPO:probinson[2012-07-16]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0003355	OMIM:249650	IEA					P	HPO:iea[2009-02-17]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0000007	OMIM:249650	IEA					I	HPO:iea[2009-02-17]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0002705	OMIM:249650	TAS					P	HPO:skoehler[2015-12-30]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0000218	OMIM:249650	IEA					P	HPO:iea[2009-02-17]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0005280	OMIM:249650	IEA					P	HPO:iea[2009-02-17]
OMIM:249650	Mercaptolactate-Cysteine disulfiduria		HP:0001249	OMIM:249650	IEA					P	HPO:iea[2009-02-17]
OMIM:620411	Palmoplantar keratoderma, epidermolytic, 2		HP:0002212	PMID:11286630	PCS		0/1			P	HPO:probinson[2024-03-01]
OMIM:620411	Palmoplantar keratoderma, epidermolytic, 2		HP:0011463	PMID:11286630	PCS		3/3			C	HPO:probinson[2024-03-01]
OMIM:620411	Palmoplantar keratoderma, epidermolytic, 2		HP:0000972	PMID:11286630	PCS	HP:0011463				P	HPO:probinson[2024-03-01]
OMIM:620411	Palmoplantar keratoderma, epidermolytic, 2		HP:0000972	PMID:11286630	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:620411	Palmoplantar keratoderma, epidermolytic, 2		HP:0000006	PMID:11286630	PCS					I	HPO:probinson[2024-03-01]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0000252	PMID:23141293	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-05-30]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0000750	PMID:23141293	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-05-30]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0011342	PMID:23141293	PCS		2/2			P	HPO:probinson[2021-05-30]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0001252	PMID:23141293	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-05-30]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0001263	PMID:23141293	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-05-30]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0034465	PMID:23141293	PCS		2/2			P	HPO:probinson[2022-12-18]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0410309	PMID:23141293	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-30];HPO:probinson[2024-02-09]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0000007	PMID:23141293	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:204750	Alpha-aminoadipic and alpha-ketoadipic aciduria		HP:0007018	PMID:23141293	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-05-30]
OMIM:300244	Terminal osseous dysplasia		HP:0000286	PMID:20598277	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0000582	PMID:20598277	PCS		2/4			P	HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0001156	PMID:20598277	PCS		5/6			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0003330	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0100490	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0005011	OMIM:300244	IEA		HP:0040283			P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0011355	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0012471	PMID:20598277	PCS		2/3			P	HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0002814	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0000437	PMID:20598277	PCS		2/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0000316	PMID:20598277	PCS		4/6			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0000612	PMID:20598277	PCS		1/7			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0030084	PMID:20598277	PCS		4/5			P	HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0001863	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0001423	PMID:20598277	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0001000	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0000175	PMID:20598277	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0000272	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0010675	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0000191	PMID:20598277	PCS		2/3			P	HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0010614	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0010660	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0000506	PMID:20598277	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0002828	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0000508	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0001836	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0001159	OMIM:300244	IEA		3/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300244	Terminal osseous dysplasia		HP:0000369	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0004987	OMIM:300244	IEA		HP:0040283			P	HPO:skoehler[2013-01-09]
OMIM:300244	Terminal osseous dysplasia		HP:0001831	OMIM:300244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:600919	Cardiac arrhythmia, ankyrin-B-related		HP:0005110	OMIM:600919	TAS					P	HPO:probinson[2012-04-11]
OMIM:600919	Cardiac arrhythmia, ankyrin-B-related		HP:0001657	PMID:15178757	PCS		4/25			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-09]
OMIM:600919	Cardiac arrhythmia, ankyrin-B-related		HP:0001279	PMID:15178757	PCS		4/25			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-09]
OMIM:600919	Cardiac arrhythmia, ankyrin-B-related		HP:0001645	PMID:15178757	PCS		3/25			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-09]
OMIM:600919	Cardiac arrhythmia, ankyrin-B-related		HP:0000006	PMID:15178757	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-07-09]
OMIM:600919	Cardiac arrhythmia, ankyrin-B-related		HP:0001688	PMID:15178757	PCS		1/25			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-09]
OMIM:619290	Mahvash disease		HP:0030688	PMID:25695890;PMID:19657311	PCS		3/3			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619290	Mahvash disease		HP:0002321	PMID:19657311	PCS		1/1			P	HPO:probinson[2021-06-19]
OMIM:619290	Mahvash disease		HP:0100027	PMID:25695890	PCS		1/3			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619290	Mahvash disease		HP:0003581	PMID:25695890;PMID:19657311	PCS		4/4			C	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619290	Mahvash disease		HP:0000007	PMID:19657311	PCS					I	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619290	Mahvash disease		HP:4000061	PMID:25695890	PCS		3/3			P	HPO:probinson[2021-07-16]
OMIM:619290	Mahvash disease		HP:0001962	PMID:19657311	PCS		1/1			P	HPO:probinson[2021-06-19]
OMIM:619290	Mahvash disease		HP:0005978	PMID:25695890	PCS		1/3			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619290	Mahvash disease		HP:0002027	PMID:25695890	PCS		1/3			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:618830	Autism, susceptibility to, 20		HP:0012760	OMIM:618830	TAS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618830	Autism, susceptibility to, 20		HP:0001263	OMIM:618830	TAS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618830	Autism, susceptibility to, 20		HP:0000729	OMIM:618830	TAS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618830	Autism, susceptibility to, 20		HP:0000722	OMIM:618830	TAS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618830	Autism, susceptibility to, 20		HP:0007018	OMIM:618830	TAS					P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618830	Autism, susceptibility to, 20		HP:0000006	OMIM:618830	TAS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:252270	Myelodysplasia and leukemia syndrome with monosomy 7		HP:0004808	OMIM:252270;PMID:11172908	PCS		11/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-08-26]
OMIM:252270	Myelodysplasia and leukemia syndrome with monosomy 7		HP:0000007	OMIM:252270	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:252270	Myelodysplasia and leukemia syndrome with monosomy 7		HP:0005518	OMIM:252270	IEA					P	HPO:iea[2009-02-17]
OMIM:252270	Myelodysplasia and leukemia syndrome with monosomy 7		HP:0001873	OMIM:252270	IEA					P	HPO:iea[2009-02-17]
OMIM:252270	Myelodysplasia and leukemia syndrome with monosomy 7		HP:0002863	PMID:11172908	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-08-26]
OMIM:176430	Premature chromatid separation trait		HP:0200024	OMIM:176430	IEA					P	HPO:skoehler[2009-02-17]
OMIM:176430	Premature chromatid separation trait		HP:0000006	OMIM:176430	IEA					I	HPO:iea[2009-02-17]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000286	PMID:17220172;PMID:17331980;PMID:28619360;PMID:30690882	PCS		2/5			P	HPO:probinson[2019-07-07];ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001254	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002421	PMID:17331980	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0003236	PMID:17220172;PMID:28619360	PCS		2/2			P	HPO:skoehler[2013-04-01];HPO:probinson[2019-07-07];ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001250	PMID:17331980;PMID:28619360	PCS		1/2			P	HPO:probinson[2019-07-06];ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001252	PMID:17331980;PMID:17220172;PMID:28619360	PCS		3/3			P	HPO:skoehler[2013-04-01];HPO:probinson[2024-04-25];ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0003196	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001251	PMID:17220172	PCS	HP:0003593	1/1			P	HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0003593	PMID:17331980;PMID:17220172;PMID:28619360	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0034337	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0012301	PMID:17331980;PMID:17220172;PMID:28619360	PCS		3/3			P	HPO:probinson[2019-07-06];ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000316	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0007366	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0040019	PMID:28619360	PCS		2/3			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002335	PMID:30690882	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001249	PMID:28619360	PCS		1/1			P	HPO:skoehler[2013-04-01];HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001249	PMID:17220172	PCS	HP:0003593	1/1			P	HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001249	PMID:17331980	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001249	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001188	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0031956	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000252	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001344	PMID:17331980	PCS		1/1			P	HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002673	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001263	PMID:17331980;PMID:17220172;PMID:28619360	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0012385	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0006380	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0034199	PMID:30690882	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0010880	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000007	PMID:17220172	PCS					I	HPO:skoehler[2013-04-01];HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0006466	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001137	PMID:17220172	PCS	HP:0003593	1/1			P	HPO:skoehler[2013-04-01];HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001137	PMID:28619360	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001137	PMID:17331980	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0003438	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000369	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001336	PMID:17331980	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000445	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0025045	PMID:17331980	PCS		1/1			P	HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0008947	PMID:17331980;PMID:28619360	PCS	HP:0003593	4/4			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-06];HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0006846	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0011918	PMID:17220172	PCS		1/1			P	HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000582	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000463	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002002	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001310	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001272	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06];HPO:probinson[2019-07-06];HPO:probinson[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001272	PMID:17220172	PCS		1/1			P	HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000260	PMID:17331980;PMID:17220172;PMID:30690882	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001274	PMID:30690882	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0010665	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0034360	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0008150	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:skoehler[2013-04-01];HPO:probinson[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001508	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0032220	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000657	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0007420	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0007267	PMID:17331980	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001305	PMID:30690882	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002119	PMID:17331980;PMID:28619360	PCS		1/2			P	HPO:probinson[2019-07-07];HPO:skoehler[2013-04-01];HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0008115	PMID:17220172	PCS		1/1			P	HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002910	PMID:17220172;PMID:28619360	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0004855	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002650	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002650	PMID:28619360	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002650	PMID:17331980	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002650	PMID:17220172	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002133	PMID:17220172	PCS	HP:0003593	1/1			P	HPO:skoehler[2013-04-01];HPO:probinson[2019-07-07]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002133	PMID:28619360	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002133	PMID:17331980	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002133	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001762	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001762	PMID:17331980	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001762	PMID:17220172	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000233	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0002376	PMID:17331980;PMID:17220172;PMID:28619360	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000474	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0005484	PMID:17220172	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000470	PMID:17331980;PMID:17220172;PMID:30690882	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0005280	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0005280	PMID:30690882	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0005280	PMID:17331980	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0005280	PMID:17220172	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0001511	PMID:17331980;PMID:17220172;PMID:28619360;PMID:30690882	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000347	PMID:28619360	PCS	HP:0011463	1/1			P	HPO:probinson[2019-07-06]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000347	PMID:28619360	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000347	PMID:30690882	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000347	PMID:17331980	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:611182	Congenital disorder of glycosylation, type IIh		HP:0000347	PMID:17220172	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-25]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0003510	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000486	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000463	PMID:26637980	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0003196	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0002020	PMID:26637980	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0012448	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001270	PMID:26637980	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001508	PMID:26637980	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0012471	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0008551	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000059	PMID:26637980	PCS			FEMALE		P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000457	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000358	PMID:26637980	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001601	PMID:26637980	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001249	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001385	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000494	PMID:26637980	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000175	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000252	OMIM:616835	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000750	PMID:26637980	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0002750	PMID:26637980	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000430	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0011968	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0002097	PMID:26637980	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0011800	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0005280	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001518	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000308	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0005819	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001537	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000348	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000824	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0006443	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000405	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000823	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0002007	PMID:26637980	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0002205	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0001852	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000006	OMIM:616835	IEA					I	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000402	PMID:26637980	PCS					P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0002786	PMID:26637980	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000028	PMID:26637980	PCS			MALE		P	HPO:probinson[2017-06-17]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0000621	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616835	Meier-Gorlin syndrome 6		HP:0009879	OMIM:616835	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609915	Cardiomyopathy, dilated, 1Q		HP:0003581	PMID:16228230	PCS		16/16			C	HPO:probinson[2022-07-04]
OMIM:609915	Cardiomyopathy, dilated, 1Q		HP:0000006	PMID:16228230	PCS					I	HPO:probinson[2022-07-04]
OMIM:609915	Cardiomyopathy, dilated, 1Q		HP:0001644	PMID:16228230	PCS		16/16			P	HPO:probinson[2022-07-04]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0010648	PMID:21778426;PMID:29392890	PCS		12/48			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0410151	PMID:23608731	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0010646	PMID:29392890	PCS		1/22			P	HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0010886	PMID:21217753	PCS		13/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0100645	PMID:21217753	PCS		2/17	FEMALE		P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0012432	PMID:29392890;PMID:22167769	PCS		22/56			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000518	PMID:29392890	PCS		4/19			P	HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002619	PMID:21282188;PMID:22167769;PMID:21217753	PCS		51/91			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000316	PMID:21778426;PMID:29392890;PMID:22167769;PMID:32154675;PMID:21217753	PCS		36/130			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001647	PMID:22167769	PCS	HP:0003577	1/33			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001643	PMID:21217753	PCS		1/33			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000278	PMID:29392890	PCS		6/29			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001642	PMID:21217753	PCS	HP:0003577	1/33			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001763	PMID:21778426;PMID:29392890;PMID:22167769;PMID:32154675	PCS		99/139			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002138	PMID:29392890	PCS		4/42			P	HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000175	PMID:21778426	PCS		0/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002076	PMID:22167769	PCS		15/30			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001382	PMID:21778426;PMID:29392890;PMID:32154675;PMID:21217753	PCS		30/116			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001065	PMID:29392890;PMID:22167769;PMID:32154675	PCS		48/135			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001263	PMID:21217753	PCS		0/27			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0012499	PMID:21778426	PCS		1/42			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0011645	PMID:21778426	PCS		8/42			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0012385	PMID:21778426;PMID:29392890;PMID:22167769	PCS		13/106			P	HPO:skoehler[2013-10-22];HP:probinson[2019-04-13];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0100775	PMID:21778426;PMID:29392890	PCS		11/18			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001537	PMID:32154675;PMID:21217753	PCS		12/39			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000689	PMID:29392890	PCS		8/23			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000766	PMID:22167769;PMID:32154675;PMID:21217753	PCS		21/72			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002108	PMID:32154675	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000768	PMID:21778426	PCS		1/8		HP:0012825	P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001659	PMID:32154675	PCS		4/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000520	PMID:29392890	PCS		2/29			P	HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002107	PMID:29392890	PCS		1/29			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001653	PMID:21217753	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0008843	PMID:21217753	PCS		4/26			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000006	PMID:21217753	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001699	PMID:29392890	PCS		16/57			P	HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0005116	PMID:32154675;PMID:21217753	PCS		11/26			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0003179	PMID:29392890;PMID:22167769	PCS		14/40			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000023	PMID:32154675;PMID:21217753	PCS		12/39			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0012727	PMID:22167769	PCS		28/39			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0005112	PMID:21778426;PMID:29392890;PMID:22167769	PCS		13/151			P	HP:probinson[2019-04-13];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001075	PMID:21778426;PMID:29392890	PCS		9/44			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0005110	PMID:29392890;PMID:22167769	PCS		16/66			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000939	PMID:32154675	PCS		0/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000938	PMID:32154675	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0004938	PMID:22167769	PCS		8/16			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000139	PMID:22167769;PMID:21217753	PCS		16/27	FEMALE		P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000978	PMID:21778426;PMID:29392890;PMID:22167769	PCS		26/78			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000977	PMID:29392890;PMID:22167769;PMID:32154675;PMID:21217753	PCS		60/111			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002758	PMID:21778426;PMID:32154675;PMID:21217753	PCS		33/63			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000218	PMID:21778426;PMID:32154675	PCS		12/28			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0004933	PMID:21778426	PCS	HP:0003581	13/42			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000577	PMID:29392890	PCS					P	HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0008419	PMID:29392890;PMID:22167769;PMID:21217753	PCS		94/128			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001166	PMID:29392890;PMID:22167769;PMID:32154675	PCS		42/125			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0003302	PMID:29392890	PCS		19/61			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001363	PMID:29392890;PMID:21217753	PCS		1/58			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001762	PMID:29392890	PCS		4/31			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002650	PMID:21778426;PMID:29392890;PMID:22167769;PMID:32154675;PMID:21217753	PCS		103/199		HP:0012825	P	HPO:probinson[2021-05-23];HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000276	PMID:21778426;PMID:21217753	PCS		11/18			P	HPO:probinson[2021-05-23];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000193	PMID:21778426;PMID:32154675;PMID:21217753	PCS		14/46			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01];HP:probinson[2019-04-13];HPO:probinson[2024-03-31]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000592	PMID:32154675	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000272	PMID:21778426;PMID:29392890	PCS		17/49			P	HP:probinson[2019-04-13];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0005086	PMID:21217753	PCS		13/26			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001083	PMID:32154675;PMID:21217753	PCS		0/49			P	HP:probinson[2019-04-13];HPO:probinson[2024-03-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001519	PMID:22167769;PMID:32154675	PCS		15/52			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001712	PMID:29392890	PCS		7/34			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0002647	PMID:32154675;PMID:21217753	PCS		12/32			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001714	PMID:22167769	PCS		6/33			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0000268	PMID:29392890	PCS		9/28			P	HP:probinson[2019-04-13]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0006687	PMID:21778426;PMID:29392890;PMID:22167769	PCS		25/77			P	HP:probinson[2019-04-13];HP:probinson[2019-04-13];HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0004944	PMID:22167769;PMID:32154675	PCS		8/27			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001631	PMID:22167769	PCS	HP:0003577	1/33			P	HPO:probinson[2021-05-23]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0001634	PMID:21778426;PMID:32154675	PCS		7/45			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613795	Loeys-Dietz syndrome 3		HP:0004942	PMID:29392890;PMID:32154675;PMID:21217753	PCS		67/109			P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13];HP:probinson[2019-04-13];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:153840	Macular dystrophy, vitelliform, 1		HP:0001123	OMIM:153840	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:153840	Macular dystrophy, vitelliform, 1		HP:0003584	OMIM:153840	TAS					C	HPO:skoehler[2009-02-17]
OMIM:153840	Macular dystrophy, vitelliform, 1		HP:0007663	OMIM:153840	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:153840	Macular dystrophy, vitelliform, 1		HP:0000505	OMIM:153840	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:153840	Macular dystrophy, vitelliform, 1		HP:0007677	OMIM:153840	TAS					P	HPO:skoehler[2009-02-17]
OMIM:153840	Macular dystrophy, vitelliform, 1		HP:0007754	OMIM:153840	IEA					P	HPO:skoehler[2015-01-27]
OMIM:153840	Macular dystrophy, vitelliform, 1		HP:0000006	OMIM:153840	TAS					I	HPO:skoehler[2009-02-17]
OMIM:248200	Stargardt disease 1		HP:0000608	OMIM:248200	TAS					P	HPO:probinson[2009-02-17]
OMIM:248200	Stargardt disease 1		HP:0008035	OMIM:248200	TAS					P	HPO:probinson[2009-02-17]
OMIM:248200	Stargardt disease 1		HP:0000007	OMIM:248200	TAS					I	HPO:probinson[2009-02-17]
OMIM:248200	Stargardt disease 1		HP:0011504	OMIM:248200	TAS		15/15			P	HPO:probinson[2014-01-28]
OMIM:257320	Lissencephaly 2		HP:0000252	PMID:10973257	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0000340	PMID:10973257	PCS					P	HPO:probinson[2012-05-01];HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0001321	PMID:10973257	PCS					P	HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0002197	PMID:10973257	PCS					P	HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0001252	PMID:10973257	PCS	HP:0003577	6/6			P	HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0001263	PMID:10973257	PCS		6/6			P	HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0006818	PMID:6476009	PCS					P	HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0012110	PMID:10973257	PCS					P	HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0006891	OMIM:257320	IEA					P	HPO:skoehler[2019-04-18]
OMIM:257320	Lissencephaly 2		HP:0000426	OMIM:257320	TAS					P	HPO:iea[2009-02-17]
OMIM:257320	Lissencephaly 2		HP:0001339	PMID:10973257	PCS		6/6			P	HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0000007	PMID:10973257	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-09]
OMIM:257320	Lissencephaly 2		HP:0001004	PMID:10973257	PCS	HP:0003577				P	HP:probinson[2019-04-09];HP:probinson[2019-04-09]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0000252	PMID:23872636	PCS		1/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0002257	PMID:23872636	PCS		2/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0001696	PMID:23872636	PCS		3/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0001651	PMID:23872636	PCS		1/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0002110	PMID:23872636	PCS		5/12			P	HPO:skoehler[2013-11-18]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0003593	PMID:23872636	PCS					C	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0002020	PMID:23872636	PCS		1/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0031245	PMID:23872636	PCS		2/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0034315	PMID:23872636	PCS		1/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0011108	PMID:23872636	PCS		7/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0012265	PMID:23872636	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0012263	PMID:23872636	PCS		6/7			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0000789	PMID:23872636	PCS		5/5			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0000403	PMID:23872636	PCS		9/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0000007	PMID:23872636	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0001748	PMID:23872636	PCS		1/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0006532	PMID:23872636	PCS		1/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0006510	PMID:23872636	PCS		3/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0002205	PMID:23872636	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0002643	PMID:23872636	PCS		7/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:615482	Ciliary dyskinesia, primary, 25		HP:0004469	PMID:23872636	PCS		1/12			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:614944	Deafness, autosomal recessive 84B		HP:0003577	PMID:23122586	PCS		3/3			C	HPO:probinson[2022-09-25]
OMIM:614944	Deafness, autosomal recessive 84B		HP:0000407	PMID:23122586	PCS		7/7			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:614944	Deafness, autosomal recessive 84B		HP:0001756	PMID:23122586	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-09-25]
OMIM:614944	Deafness, autosomal recessive 84B		HP:0000007	PMID:23122586	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2022-09-25]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000286	PMID:35567594	PCS		3/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000486	PMID:35567594	PCS		4/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000540	PMID:35567594	PCS		3/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000089	PMID:35567594	PCS		1/22		HP:0012833	P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0001252	PMID:35567594	PCS	HP:0003623	4/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0003593	PMID:35567594	PCS					C	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000319	PMID:35567594	PCS		6/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000739	PMID:35567594	PCS		2/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000414	PMID:35567594	PCS		9/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000219	PMID:35567594	PCS		7/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0002414	PMID:35567594	PCS		1/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000256	PMID:35567594	PCS		2/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0001169	PMID:35567594	PCS		6/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000358	PMID:35567594	PCS		4/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000297	PMID:35567594	PCS		5/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000098	PMID:35567594	PCS		4/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000054	PMID:35567594	PCS		1/4			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000252	PMID:35567594	PCS		1/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000750	PMID:35567594	PCS		16/19			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0031936	PMID:35567594	PCS		8/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0011968	PMID:35567594	PCS		5/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000490	PMID:35567594	PCS		10/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0001263	PMID:35567594	PCS		22/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0002591	PMID:35567594	PCS		4/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0009909	PMID:35567594	PCS		4/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000470	PMID:35567594	PCS		3/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0011822	PMID:35567594	PCS		6/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0100025	PMID:35567594	PCS		8/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000729	PMID:35567594	PCS		9/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0007018	PMID:35567594	PCS		6/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000006	PMID:35567594	PCS					I	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0001513	PMID:35567594	PCS		7/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000369	PMID:35567594	PCS		4/22			P	HPO:probinson[2024-02-15]
OMIM:620439	Intellectual developmental disorder, autosomal dominant 72		HP:0000049	PMID:35567594	PCS		1/14			P	HPO:probinson[2024-02-15]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002069	PMID:27866705	PCS		3/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002267	PMID:27866705	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0006989	PMID:27866705	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0010804	PMID:27866705	PCS		3/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0032794	PMID:27866705	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000280	PMID:27866705	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000739	PMID:27866705	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0100702	PMID:27866705	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0007089	PMID:27866705	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0020221	PMID:27866705	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0001305	PMID:27866705	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000238	PMID:27866705	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002119	PMID:27866705	PCS		2/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000752	PMID:27866705	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002514	PMID:27866705	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000215	OMIM:617281	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0001347	OMIM:617281	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0003623	PMID:27866705	PCS		3/3			C	HPO:probinson[2023-04-07];HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0008936	OMIM:617281	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002135	PMID:27866705	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0001320	PMID:27866705	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000252	PMID:27866705	PCS		3/3			P	HPO:skoehler[2019-04-18]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002510	PMID:27866705	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0001344	PMID:27866705	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002353	PMID:27866705	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000574	PMID:27866705	PCS		3/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000232	PMID:27866705	PCS		3/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000194	PMID:27866705	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0001263	PMID:27866705	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0012736	OMIM:617281	TAS					P	HP:probinson[2019-01-04]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0011344	PMID:27866705	PCS		3/3			P	HPO:probinson[2023-04-07];HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0032792	PMID:27866705	PCS		2/3			P	HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000448	PMID:27866705	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000007	PMID:27866705	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-07]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0200134	PMID:27866705	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000527	PMID:27866705	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000648	OMIM:617281	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0002007	OMIM:617281	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000400	PMID:27866705	PCS		3/3			P	HPO:skoehler[2019-04-18]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0000322	PMID:27866705	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0001257	OMIM:617281	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617281	Epileptic encephalopathy, early infantile, 49		HP:0001336	PMID:27866705	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:132500	Epistaxis, hereditary		HP:0000421	OMIM:132500	IEA					P	HPO:iea[2009-02-17]
OMIM:132500	Epistaxis, hereditary		HP:0000006	OMIM:132500	IEA					I	HPO:iea[2009-02-17]
OMIM:603592	Xanthinuria, type II		HP:0003621	PMID:17368066	PCS		3/5			C	HPO:probinson[2022-05-29]
OMIM:603592	Xanthinuria, type II		HP:0003596	PMID:17368066	PCS		1/5			C	HPO:probinson[2022-05-29]
OMIM:603592	Xanthinuria, type II		HP:0010934	PMID:17368066	PCS		3/3			P	HPO:probinson[2022-05-29]
OMIM:603592	Xanthinuria, type II		HP:0011814	PMID:17368066	PCS		3/3			P	HPO:probinson[2022-05-29]
OMIM:603592	Xanthinuria, type II		HP:0000083	OMIM:603592	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603592	Xanthinuria, type II		HP:0011463	PMID:17368066	PCS		1/5			C	HPO:probinson[2022-05-29]
OMIM:603592	Xanthinuria, type II		HP:0034333	OMIM:603592	TAS					P	HPO:probinson[2022-09-05]
OMIM:603592	Xanthinuria, type II		HP:0000007	PMID:11302742	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-20]
OMIM:603592	Xanthinuria, type II		HP:0010933	PMID:17368066;PMID:11302742	PCS		5/5			P	HPO:probinson[2022-05-29]
OMIM:603592	Xanthinuria, type II		HP:0003537	PMID:11302742	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-20]
OMIM:603592	Xanthinuria, type II		HP:0000787	PMID:17368066	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-29]
OMIM:603592	Xanthinuria, type II		HP:0003326	PMID:17368066	PCS		2/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0010628	PMID:20975055	PCS		3/33			P	HPO:probinson[2018-03-07]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0000365	PMID:20975055	PCS		6/33			P	HPO:probinson[2018-03-07]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0030664	PMID:20975055	PCS		12/18			P	HPO:skoehler[2015-12-30]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0008970	PMID:20975055	PCS					P	HPO:skoehler[2015-01-27]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0003691	PMID:8328457	PCS		33/33			P	HPO:probinson[2015-12-28]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0003581	PMID:20975055	PCS					C	HPO:probinson[2018-03-07]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0009027	PMID:20975055	PCS		26/33			P	HPO:probinson[2018-03-07]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0003749	PMID:20975055	PCS		3/33			P	HPO:probinson[2018-03-07]
OMIM:158901	Facioscapulohumeral muscular dystrophy 2		HP:0010984	PMID:23143600	PCS					I	HPO:probinson[2018-03-07];HPO:probinson[2021-10-03]
OMIM:136000	Fingerprints, absence of		HP:0001217	OMIM:136000	TAS					P	HPO:probinson[2012-06-04]
OMIM:136000	Fingerprints, absence of		HP:0007455	OMIM:136000	TAS					P	HPO:probinson[2012-06-04]
OMIM:136000	Fingerprints, absence of		HP:0000006	OMIM:136000	TAS					I	HPO:probinson[2009-02-17]
OMIM:136000	Fingerprints, absence of		HP:0010765	OMIM:136000	TAS				HP:0012825	P	HPO:probinson[2012-06-04]
OMIM:619521	Epilepsy, idiopathic generalized, susceptibility to, 18		HP:0000750	PMID:30127718	PCS		2/2		HP:0012825	P	HPO:probinson[2021-10-24]
OMIM:619521	Epilepsy, idiopathic generalized, susceptibility to, 18		HP:0001662	PMID:30127718	PCS		2/2			P	HPO:probinson[2021-10-24]
OMIM:619521	Epilepsy, idiopathic generalized, susceptibility to, 18		HP:0003593	PMID:30127718	IEA		2/2			C	HPO:probinson[2021-10-24]
OMIM:619521	Epilepsy, idiopathic generalized, susceptibility to, 18		HP:0032794	PMID:30127718	PCS	HP:0003593	2/2			P	HPO:probinson[2021-10-24]
OMIM:619521	Epilepsy, idiopathic generalized, susceptibility to, 18		HP:0000006	PMID:30127718	PCS					I	HPO:probinson[2021-10-24];HPO:probinson[2021-10-24]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001212	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000486	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0012745	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000518	PMID:18784092	PCS		3/21			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0010055	PMID:18784092	PCS		1/21			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001845	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0003745	PMID:18784092	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0002553	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000252	PMID:18784092	PCS		14/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0025493	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0004970	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000490	PMID:18784092	PCS		2/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000407	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000767	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0004209	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000006	PMID:18784092	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000248	PMID:18784092	PCS		3/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000369	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001337	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000582	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000343	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000463	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001156	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0002121	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001669	PMID:18784092	PCS	HP:0003577	1/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000733	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000219	PMID:18784092	PCS		3/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000218	PMID:18784092	PCS		3/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000179	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000750	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0002650	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000233	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0005487	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000193	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001680	PMID:18784092	PCS		1/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000470	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0040053	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0011623	PMID:18784092	PCS	HP:0003577	1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0100716	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001956	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0002007	OMIM:612474	TAS					P	HPO:skoehler[2012-11-16]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000347	PMID:18784092	PCS		4/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0002069	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000286	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001250	PMID:18784092	PCS		5/21			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001252	PMID:18784092	PCS		5/21			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000319	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0011220	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000717	PMID:18784092	PCS		1/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0003829	OMIM:612474	TAS					I	HPO:skoehler[2012-11-16]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001647	PMID:18784092	PCS		1/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000316	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000954	PMID:18784092	PCS		3/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0020045	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0009942	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001643	PMID:18784092	PCS		2/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001763	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000311	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001249	PMID:18784092	PCS					P	HPO:skoehler[2013-06-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0020206	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001660	PMID:18784092	PCS	HP:0003577	1/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001382	PMID:18784092	PCS		5/42			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001263	PMID:18784092	PCS		16/21			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000691	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0010112	PMID:18784092	PCS	HP:0003577	1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0012385	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000448	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000601	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000568	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001659	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000325	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000687	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000540	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000262	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001508	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0011682	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0009882	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000414	OMIM:612474	TAS					P	HPO:skoehler[2012-11-16]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0009765	PMID:18784092	PCS		2/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000411	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0009921	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0008936	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001883	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0025313	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000272	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0002292	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0010698	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0010695	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0005280	PMID:18784092	PCS		5/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0011304	PMID:18784092	PCS		1/21			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000708	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0100753	OMIM:612474	TAS					P	HPO:skoehler[2012-11-16]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000426	PMID:18784092	PCS		3/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000307	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000664	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0001631	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000303	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:612474	Chromosome 1q21.1 deletion syndrome, 1.35-mb		HP:0000269	PMID:18784092	PCS		1/21			P	HPO:probinson[2022-11-08]
OMIM:103050	Adenylosuccinase deficiency		HP:0003577	PMID:18524658	PCS		2/7			C	HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0002301	PMID:18524658	PCS		1/7			P	HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0002540	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0000343	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0000486	PMID:18524658	PCS		4/7			P	HPO:probinson[2012-03-12];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0000463	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0001272	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0001250	OMIM:103050	PCS					P	HPO:probinson[2012-04-11]
OMIM:103050	Adenylosuccinase deficiency		HP:0002066	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0001252	PMID:18524658	PCS		5/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0003196	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0006808	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0003593	PMID:18524658;OMIM:103050	PCS		13/17			C	HPO:probinson[2023-01-31];HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0001290	OMIM:103050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:103050	Adenylosuccinase deficiency		HP:0040082	OMIM:103050	TAS		HP:0040283			P	HPO:skoehler[2014-11-27]
OMIM:103050	Adenylosuccinase deficiency		HP:0000639	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0000319	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0000718	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0000817	PMID:18524658	PCS		5/7			P	HPO:skoehler[2012-10-09];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0000717	OMIM:103050	IEA					P	HPO:skoehler[2009-02-17]
OMIM:103050	Adenylosuccinase deficiency		HP:0000219	OMIM:103050	PCS		20/20			P	HPO:skoehler[2013-06-04];HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0003429	PMID:18524658	PCS		5/7			P	HPO:skoehler[2012-10-09];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0000752	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0001348	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0001249	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0003623	PMID:18524658	PCS		2/7			C	HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0002179	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0003202	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0000154	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0002059	PMID:18524658	PCS		6/7			P	HPO:skoehler[2012-10-09];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0000252	PMID:18524658	PCS		5/7			P	HPO:probinson[2012-03-12];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0000750	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0005487	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0001263	PMID:18524658	PCS		7/7			P	HPO:skoehler[2012-10-09];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0011344	OMIM:103050	PCS					P	HPO:probinson[2012-04-11]
OMIM:103050	Adenylosuccinase deficiency		HP:0000748	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:0000007	PMID:1302001	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2023-01-31]
OMIM:103050	Adenylosuccinase deficiency		HP:0001510	OMIM:103050	PCS					P	HPO:probinson[2012-04-11]
OMIM:103050	Adenylosuccinase deficiency		HP:0001257	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0000248	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0000369	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0001336	OMIM:103050	PCS					P	HPO:probinson[2012-03-12]
OMIM:103050	Adenylosuccinase deficiency		HP:0000742	OMIM:103050	IEA					P	HPO:skoehler[2012-10-09]
OMIM:103050	Adenylosuccinase deficiency		HP:6000390	OMIM:103050	TAS					P	HPO:probinson[2024-02-27]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001332	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0004322	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002186	OMIM:314580	TAS					P	HPO:probinson[2009-02-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001250	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001252	OMIM:314580	TAS					P	HPO:skoehler[2014-11-26]
OMIM:314580	Wieacker-Wolff syndrome		HP:0010806	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001290	OMIM:314580	TAS					P	HPO:skoehler[2017-07-13]
OMIM:314580	Wieacker-Wolff syndrome		HP:0010765	OMIM:314580	TAS					P	HPO:skoehler[2017-07-13]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000319	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0003307	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0009623	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001324	OMIM:314580	TAS				HP:0012828	P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000278	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000252	PMID:31206972	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-25]
OMIM:314580	Wieacker-Wolff syndrome		HP:0011968	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001263	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0012385	OMIM:314580	TAS					P	HPO:skoehler[2013-10-22]
OMIM:314580	Wieacker-Wolff syndrome		HP:0009890	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001419	PMID:31206972;PMID:23623388	PCS		20/20			I	HPO:probinson[2020-07-25];HPO:skoehler[2013-07-17];HPO:probinson[2020-03-28]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002827	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002307	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001257	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002104	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000369	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000187	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0003577	OMIM:314580	TAS					C	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0010628	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000582	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000343	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000463	OMIM:314580	TAS					P	HPO:skoehler[2017-07-13]
OMIM:314580	Wieacker-Wolff syndrome		HP:0003693	OMIM:314580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:314580	Wieacker-Wolff syndrome		HP:0012448	OMIM:314580	TAS					P	HPO:skoehler[2013-11-28]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000657	OMIM:314580	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000218	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000774	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0005745	OMIM:314580	IEA					P	HPO:iea[2009-02-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000577	OMIM:314580	TAS					P	HPO:skoehler[2017-07-13]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002059	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000750	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002650	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001762	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001284	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000470	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002808	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000508	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002804	OMIM:314580	TAS	HP:0003577				P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0001558	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:314580	Wieacker-Wolff syndrome		HP:0000347	PMID:31206972	PCS					P	HPO:skoehler[2013-07-17];HPO:probinson[2020-07-25]
OMIM:314580	Wieacker-Wolff syndrome		HP:0002643	OMIM:314580	TAS					P	HPO:skoehler[2013-07-17]
OMIM:609054	Fanconi anemia, complementation group J		HP:0003221	PMID:16116424	PCS					P	HPO:probinson[2013-03-26]
OMIM:609054	Fanconi anemia, complementation group J		HP:0001263	PMID:16116424	PCS					P	HPO:probinson[2013-03-26]
OMIM:609054	Fanconi anemia, complementation group J		HP:0000007	PMID:16116424	PCS					I	HPO:probinson[2013-01-09]
OMIM:609054	Fanconi anemia, complementation group J		HP:0000568	PMID:16116424	PCS		4/11			P	HPO:probinson[2013-03-26]
OMIM:609054	Fanconi anemia, complementation group J		HP:0008897	PMID:16116424	PCS					P	HPO:probinson[2013-03-26]
OMIM:609054	Fanconi anemia, complementation group J		HP:0007565	PMID:16116424	PCS		8/11			P	HPO:probinson[2013-03-26]
OMIM:609054	Fanconi anemia, complementation group J		HP:0001511	PMID:16116424	PCS		3/11			P	HPO:probinson[2013-03-26]
OMIM:609054	Fanconi anemia, complementation group J		HP:0005528	PMID:16116424	PCS					P	HPO:probinson[2013-03-26]
OMIM:609054	Fanconi anemia, complementation group J		HP:0009778	PMID:16116424	PCS		3/11			P	HPO:probinson[2013-03-26]
OMIM:170900	Pernicious anemia		HP:0200118	OMIM:170900	TAS					P	HPO:probinson[2015-06-04]
OMIM:170900	Pernicious anemia		HP:0001889	OMIM:170900	TAS					P	HPO:skoehler[2010-06-20]
OMIM:170900	Pernicious anemia		HP:0000006	OMIM:170900	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:107550	Aortic arch interruption, facial palsy, and retinal coloboma		HP:0010628	OMIM:107550	TAS					P	HPO:skoehler[2009-02-17]
OMIM:107550	Aortic arch interruption, facial palsy, and retinal coloboma		HP:0000480	OMIM:107550	TAS					P	HPO:skoehler[2015-07-19]
OMIM:107550	Aortic arch interruption, facial palsy, and retinal coloboma		HP:0010817	OMIM:107550	TAS					P	HPO:probinson[2009-02-17]
OMIM:107550	Aortic arch interruption, facial palsy, and retinal coloboma		HP:0001680	OMIM:107550	TAS					P	HPO:probinson[2009-02-17]
OMIM:107550	Aortic arch interruption, facial palsy, and retinal coloboma		HP:0011611	OMIM:107550	TAS					P	HPO:probinson[2009-02-17]
OMIM:107550	Aortic arch interruption, facial palsy, and retinal coloboma		HP:0000006	OMIM:107550	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:107550	Aortic arch interruption, facial palsy, and retinal coloboma		HP:0001116	OMIM:107550	TAS					P	HPO:probinson[2009-02-17]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002289	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0001531	PMID:9096364	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0003212	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0001890	PMID:9096364	PCS		0/1			P	HPO:skoehler[2015-08-02];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0100651	PMID:17196245	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0030812	PMID:17196245	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0011220	PMID:24116927	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0100646	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0011120	PMID:24116927	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002718	PMID:9096364	PCS		1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002716	PMID:9096364	PCS	HP:0003593	1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002716	PMID:17196245	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002716	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0003765	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002113	PMID:17196245	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0005403	PMID:9096364	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002232	PMID:24116927	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0010976	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0032170	PMID:24116927	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0009098	PMID:9096364	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0031382	PMID:9096364	PCS		1/1			P	HPO:probinson[2020-10-18];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0033582	PMID:24116927	PCS		1/1			P	HPO:probinson[2021-02-13]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0040189	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0011473	PMID:23416241;PMID:17196245	PCS		2/2			P	HPO:skoehler[2015-08-02];HPO:probinson[2020-10-18];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0033222	PMID:9096364	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0100658	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0001878	PMID:17196245	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0000007	PMID:9096364	PCS					I	HPO:probinson[2013-02-23]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002848	PMID:24116927	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0000964	PMID:23416241;PMID:17196245;PMID:24116927	PCS		3/3		HP:0012828	P	HPO:skoehler[2015-08-02];HPO:probinson[2020-10-18];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0001019	PMID:23416241	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0000821	PMID:17196245	PCS		1/1			P	HPO:skoehler[2015-08-02];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0004429	PMID:9096364	PCS		1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002205	OMIM:606367;PMID:24116927	PCS		11/11			P	HPO:skoehler[2015-08-02];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0001433	PMID:9096364	PCS	HP:0003593	1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0001433	PMID:17196245	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002720	PMID:9096364	PCS		1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002841	PMID:9096364	PCS		1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002028	PMID:9096364	PCS	HP:0003593	1/1			P	HPO:probinson[2013-02-23];HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002028	PMID:17196245	PCS		1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002028	PMID:24116927	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-18]
OMIM:606367	Immunodeficiency 41 with lymphoproliferation and autoimmunity		HP:0002721	PMID:9096364	PCS					P	HPO:skoehler[2015-08-02];HPO:probinson[2020-10-18]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002069	PMID:17033963	PCS		1/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001298	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0003236	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001332	OMIM:610505	TAS					P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0005157	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001250	OMIM:610505	IEA					P	HPO:iea[2009-02-17]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001252	PMID:17033963	PCS		2/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001251	OMIM:610505	TAS					P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002240	OMIM:610505	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001290	OMIM:610505	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0032653	PMID:17033963	PCS		1/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0100543	OMIM:610505	TAS					P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0008872	OMIM:610505	IEA					P	HPO:iea[2009-02-17]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001987	PMID:17033963	PCS		1/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002878	PMID:17033963	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002119	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001522	PMID:17033963	PCS		2/2			C	HPO:probinson[2023-01-21];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001324	OMIM:610505	IEA					P	HPO:iea[2009-02-17]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001643	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001644	OMIM:610505	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0003128	OMIM:610505	IEA					P	HPO:iea[2009-02-17]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0003623	PMID:17033963	PCS		2/2			C	HPO:probinson[2023-01-21];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0003201	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0011924	PMID:17033963	PCS		2/2			P	HPO:probinson[2012-06-08]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002033	PMID:17033963	PCS		1/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001263	OMIM:610505	TAS					P	HPO:skoehler[2013-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002151	PMID:17033963	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002094	PMID:17033963	PCS		1/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0011923	PMID:17033963	PCS		2/2			P	HPO:probinson[2012-06-08];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002093	OMIM:610505	IEA					P	HPO:iea[2009-02-17]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0003819	OMIM:610505	IEA					C	HPO:iea[2009-02-17]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0002902	PMID:17033963	PCS		1/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0000007	PMID:17033963	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001558	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0008347	PMID:17033963	PCS		2/2			P	HPO:probinson[2012-06-08]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001319	PMID:17033963	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0000648	OMIM:610505	TAS					P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0000505	OMIM:610505	TAS					P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0000741	PMID:17033963	PCS		1/2			P	HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001511	OMIM:610505	TAS					P	HPO:skoehler[2013-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0004900	PMID:17033963	PCS		2/2			P	HPO:probinson[2023-01-21];HPO:probinson[2023-01-21]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001337	OMIM:610505	TAS					P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001138	OMIM:610505	TAS					P	HPO:skoehler[2014-10-06]
OMIM:610505	Combined oxidative phosphorylation deficiency 3		HP:0001655	PMID:17033963	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0001695	PMID:15489853	PCS		3/32			P	HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0002094	PMID:16549640	PCS		3/25			P	HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0034304	PMID:16549640;PMID:15489853	PCS		10/36			P	HPO:probinson[2022-09-05]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0011663	PMID:15489853	PCS		32/32			P	HPO:probinson[2012-07-17];HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0034364	PMID:16549640	PCS		4/11			P	HPO:probinson[2022-09-05]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0011462	PMID:16549640	PCS					C	HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0006682	PMID:16549640	PCS		13/18			P	HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0001962	PMID:16549640	PCS		9/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0006698	OMIM:609040	TAS					P	HPO:probinson[2009-02-17]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0001279	PMID:16549640;PMID:15489853	PCS		8/39			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0006677	PMID:16549640	PCS		15/25			P	HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0000006	PMID:15489853	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0001645	PMID:15489853	PCS		1/32			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:609040	Arrhythmogenic right ventricular dysplasia, familial, 9		HP:0004756	PMID:15489853	PCS		30/32			P	HPO:probinson[2022-07-10]
OMIM:135290	Desmoid disease, hereditary		HP:0003002	PMID:10782927	PCS	HP:0003581	1/8			P	HPO:probinson[2022-07-19]
OMIM:135290	Desmoid disease, hereditary		HP:0003596	PMID:10782927	PCS		2/8			C	HPO:probinson[2022-07-19]
OMIM:135290	Desmoid disease, hereditary		HP:0003003	PMID:10782927	PCS		1/8			P	HPO:iea[2010-07-08];HPO:probinson[2022-07-19]
OMIM:135290	Desmoid disease, hereditary		HP:0011462	PMID:10782927	PCS		6/8			C	HPO:probinson[2022-07-19]
OMIM:135290	Desmoid disease, hereditary		HP:0100245	PMID:10782927	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-19]
OMIM:135290	Desmoid disease, hereditary		HP:0000006	PMID:10782927	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-19]
OMIM:135290	Desmoid disease, hereditary		HP:0200063	PMID:10782927	PCS	HP:0003581	3/8			P	HPO:probinson[2022-07-19]
OMIM:230350	Galactose epimerase deficiency		HP:0000750	PMID:9700591	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0003355	OMIM:230350	IEA					P	HPO:iea[2009-02-17]
OMIM:230350	Galactose epimerase deficiency		HP:0002013	OMIM:230350	IEA					P	HPO:iea[2009-02-17]
OMIM:230350	Galactose epimerase deficiency		HP:0001263	OMIM:230350	TAS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0001252	OMIM:230350	IEA					P	HPO:iea[2009-02-17]
OMIM:230350	Galactose epimerase deficiency		HP:0002240	OMIM:230350	IEA					P	HPO:iea[2009-02-17]
OMIM:230350	Galactose epimerase deficiency		HP:0001290	OMIM:230350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:230350	Galactose epimerase deficiency		HP:0002194	PMID:9700591	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0012023	OMIM:230350	TAS					P	HPO:probinson[2012-07-27]
OMIM:230350	Galactose epimerase deficiency		HP:0012024	PMID:9700591	PCS		1/1			P	HPO:probinson[2012-07-27];HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0001508	OMIM:230350	IEA					P	HPO:iea[2009-02-17]
OMIM:230350	Galactose epimerase deficiency		HP:0000407	OMIM:230350	IEA					P	HPO:iea[2009-02-17]
OMIM:230350	Galactose epimerase deficiency		HP:0011463	PMID:9700591	PCS		1/1			C	HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0008166	PMID:9700591	PCS		0/1			P	HPO:probinson[2022-05-22];HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0000007	PMID:9700591	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0001249	OMIM:230350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:230350	Galactose epimerase deficiency		HP:0000952	PMID:9700591	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:230350	Galactose epimerase deficiency		HP:0001744	OMIM:230350	IEA					P	HPO:iea[2009-02-17]
OMIM:616606	Ring chromosome 14 syndrome		HP:0002465	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000286	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000463	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0002384	PMID:23610869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0001252	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000581	PMID:23610869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000580	OMIM:616606	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0003593	PMID:23610869	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0001290	OMIM:616606	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000316	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000218	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0003745	OMIM:616606	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616606	Ring chromosome 14 syndrome		HP:0001249	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000457	PMID:23610869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0005469	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000252	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000494	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0002133	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000750	PMID:23610869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0002197	PMID:23610869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0001263	PMID:23610869	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000470	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0005280	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0007874	PMID:23610869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000268	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0001510	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616606	Ring chromosome 14 syndrome		HP:0007359	PMID:23610869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:616606	Ring chromosome 14 syndrome		HP:0000369	OMIM:616606	TAS					P	HPO:skoehler[2015-11-15]
OMIM:278300	Xanthinuria, type I		HP:0012330	OMIM:278300	TAS					P	HPO:skoehler[2013-09-17]
OMIM:278300	Xanthinuria, type I		HP:0004732	PMID:9153281	PCS		3/3			P	HPO:probinson[2024-08-04]
OMIM:278300	Xanthinuria, type I		HP:0010934	OMIM:278300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:278300	Xanthinuria, type I		HP:0000804	OMIM:278300	IEA					P	HPO:iea[2009-02-17]
OMIM:278300	Xanthinuria, type I		HP:0003198	OMIM:278300	IEA					P	HPO:iea[2009-02-17]
OMIM:278300	Xanthinuria, type I		HP:0000007	OMIM:278300	IEA					I	HPO:iea[2009-02-17]
OMIM:278300	Xanthinuria, type I		HP:0010933	PMID:9153281	PCS		4/4			P	HP:probinson[2019-02-12]
OMIM:278300	Xanthinuria, type I		HP:0003537	PMID:9153281	PCS		4/4			P	HPO:probinson[2024-02-27]
OMIM:278300	Xanthinuria, type I		HP:0003534	OMIM:278300	TAS					P	HPO:skoehler[2015-01-21];HPO:probinson[2024-02-27];HPO:probinson[2024-08-04]
OMIM:278300	Xanthinuria, type I		HP:6000218	PMID:9153281	PCS		4/4			P	HPO:probinson[2024-02-27]
OMIM:278300	Xanthinuria, type I		HP:0000126	OMIM:278300	IEA					P	HPO:iea[2009-02-17]
OMIM:615327	Dowling-Degos disease 2		HP:0009719	OMIM:615327	TAS					P	HPO:probinson[2015-11-25]
OMIM:615327	Dowling-Degos disease 2		HP:0045059	PMID:25229252	PCS		HP:0040283			P	HPO:skoehler[2015-11-27];HP:probinson[2019-02-23]
OMIM:615327	Dowling-Degos disease 2		HP:0007588	PMID:25229252	PCS					P	HPO:probinson[2015-11-25];HP:probinson[2019-02-23]
OMIM:615327	Dowling-Degos disease 2		HP:0007502	OMIM:615327	TAS					P	HPO:probinson[2015-11-25]
OMIM:615327	Dowling-Degos disease 2		HP:0000006	PMID:25229252	PCS					I	HPO:skoehler[2013-09-17];HP:probinson[2019-02-23]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0008936	PMID:20829227	PCS		8/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0003577	PMID:20829227	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0000252	PMID:20829227	PCS		1/9			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0000486	PMID:20829227	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0000750	PMID:20829227	PCS		9/9			P	HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0002365	PMID:20829227	PCS		8/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0002079	PMID:20829227	PCS		8/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0001250	PMID:20829227	PCS		2/9			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0001274	PMID:20829227	PCS		1/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0001263	PMID:20829227	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0033725	PMID:20829227	PCS		6/9			P	HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0000639	PMID:20829227	PCS		4/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0002539	PMID:20829227	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0001339	PMID:20829227	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0034180	PMID:20829227	PCS		8/9			P	HPO:probinson[2022-04-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0001257	PMID:20829227	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0000006	PMID:20829227	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0001249	PMID:20829227	PCS		9/9			P	HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0006821	PMID:20829227	PCS		4/9			P	HPO:probinson[2022-02-15]
OMIM:614039	Cortical dysplasia, complex, with other brain malformations 1		HP:0009879	PMID:20829227	PCS		5/9			P	HPO:probinson[2022-02-15]
OMIM:613756	Retinitis pigmentosa 49		HP:0007737	PMID:15570217	PCS		7/7			P	HPO:probinson[2020-04-27]
OMIM:613756	Retinitis pigmentosa 49		HP:0000662	PMID:15570217	PCS	HP:0011463	7/7			P	HPO:probinson[2020-04-27]
OMIM:613756	Retinitis pigmentosa 49		HP:0000007	PMID:7479749	PCS					I	HPO:probinson[2013-06-05]
OMIM:613756	Retinitis pigmentosa 49		HP:0007663	PMID:15570217	TAS		7/7			P	HPO:probinson[2020-04-27];HPO:probinson[2020-04-27]
OMIM:613756	Retinitis pigmentosa 49		HP:0007994	PMID:15570217	PCS		7/7			P	HPO:probinson[2020-04-27]
OMIM:613756	Retinitis pigmentosa 49		HP:0000510	PMID:7479749	PCS					P	HPO:probinson[2013-06-05]
OMIM:613756	Retinitis pigmentosa 49		HP:0000543	PMID:15570217	PCS		7/7			P	HPO:probinson[2020-04-27]
OMIM:613756	Retinitis pigmentosa 49		HP:0007843	PMID:15570217	PCS		7/7			P	HPO:probinson[2020-04-27]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000486	PMID:31353023	PCS		11/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0002188	PMID:31353023	PCS		5/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000023	PMID:31353023	PCS		4/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0001250	PMID:31353023	PCS		3/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0001274	PMID:31353023	PCS		1/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0002020	PMID:31353023	PCS		6/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0001290	PMID:31353023	PCS		14/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0002280	PMID:31353023	PCS		1/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0007281	PMID:31353023	PCS		4/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0001508	PMID:31353023	PCS		3/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000316	PMID:31353023	PCS		6/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0002119	PMID:31353023	PCS		5/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000218	PMID:31353023	PCS		5/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0025336	PMID:31353023	PCS					P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0003546	PMID:31353023	PCS		10/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0003202	PMID:31353023	PCS		4/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0025352	PMID:31353023	PCS					I	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000175	PMID:31353023	PCS		1/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000252	PMID:31353023	PCS		5/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000692	PMID:31353023	PCS		5/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0031936	PMID:31353023	PCS					P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0002453	PMID:31353023	PCS		2/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0002079	PMID:31353023	PCS		2/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0011968	PMID:31353023	PCS		10/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0031139	PMID:31353023	PCS	HP:0003593	10/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000729	PMID:31353023	PCS		4/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000767	PMID:31353023	PCS		3/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000348	PMID:31353023	PCS		7/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0001558	PMID:31353023	PCS	HP:0011461	3/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000505	PMID:31353023	PCS		5/15			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0002205	PMID:31353023	PCS		8/14			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0001357	PMID:31353023	PCS		5/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000248	PMID:31353023	PCS		5/16			P	HPO:probinson[2020-07-22]
OMIM:618603	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities		HP:0000006	PMID:31353023	PCS					I	HPO:probinson[2022-09-04]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0003577	PMID:8799157	PCS		9/14			C	HPO:probinson[2022-03-19]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0002164	OMIM:131960	IEA					P	HPO:iea[2009-02-17]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0011937	PMID:15982306	PCS		2/2			P	HPO:probinson[2022-03-19]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0003593	PMID:15982306	IEA		2/2			C	HPO:probinson[2022-03-19]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0033802	PMID:15982306;PMID:8799157	PCS		12/12			P	HPO:probinson[2022-03-19]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0001805	OMIM:131960	IEA					P	HPO:iea[2009-02-17]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0007494	OMIM:131960	IEA					P	HPO:iea[2009-02-17]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0008066	PMID:15982306;PMID:8799157	PCS		16/16			P	HPO:probinson[2022-03-19];HPO:probinson[2012-07-19];HPO:probinson[2022-03-19]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0011463	PMID:8799157	PCS		5/14			C	HPO:probinson[2022-03-19]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0007530	OMIM:131960	IEA					P	HPO:iea[2009-02-17]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0008404	OMIM:131960	TAS					P	HPO:skoehler[2013-05-03]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0000006	PMID:8799157	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:131960	Epidermolysis bullosa simplex with mottled pigmentation		HP:0007438	PMID:8799157	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:235200	Hemochromatosis, type 1		HP:0000044	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0002202	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001596	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0003452	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0000141	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001394	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0002240	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0011675	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0000819	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0000939	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001009	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0000953	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0002910	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001744	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001402	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001541	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001640	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0003040	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0003281	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0000007	OMIM:235200	IEA					I	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0000029	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001635	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0000802	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001638	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0002027	OMIM:235200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:235200	Hemochromatosis, type 1		HP:0000027	OMIM:235200	IEA					P	HPO:iea[2009-02-17]
OMIM:235200	Hemochromatosis, type 1		HP:0001952	OMIM:235200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618165	Bone marrow failure syndrome 5		HP:0002069	PMID:30146126	PCS		1/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0004313	PMID:30146126	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0000252	PMID:30146126	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0002750	PMID:30146126	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0004322	PMID:30146126	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0001263	PMID:30146126	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0003593	PMID:30146126	PCS		1/2			C	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0031413	PMID:30146126	PCS		2/2			P	HPO:probinson[2022-12-22];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0012133	PMID:30146126	PCS		2/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0012410	PMID:30146126	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0001903	PMID:30146126	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0000029	PMID:30146126	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0007588	PMID:30146126	PCS		2/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0008404	PMID:30146126	PCS		0/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0000135	PMID:30146126	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0001510	PMID:30146126	PCS		2/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0002206	PMID:30146126	PCS		0/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0002745	PMID:30146126	PCS		0/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0000006	PMID:30146126	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0001249	PMID:30146126	PCS		2/2			P	HPO:probinson[2022-12-22]
OMIM:618165	Bone marrow failure syndrome 5		HP:0003623	PMID:30146126	PCS		1/2			C	HPO:probinson[2022-12-22]
OMIM:610539	Gaucher disease, atypical		HP:0003148	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0002653	PMID:17919309	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0002133	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0001971	PMID:17919309	PCS		1/2			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0002376	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0003146	PMID:17919309	PCS		1/2			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0001250	OMIM:610539	TAS					P	HPO:probinson[2013-01-09]
OMIM:610539	Gaucher disease, atypical		HP:0002240	PMID:9930900;PMID:17919309	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0011813	OMIM:610539	TAS					P	HPO:probinson[2013-02-28]
OMIM:610539	Gaucher disease, atypical		HP:0002080	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0012432	PMID:17919309	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0000605	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0001903	PMID:17919309	PCS		2/2			P	HPO:probinson[2013-02-28];HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0000938	PMID:17919309	PCS		1/2			P	HPO:probinson[2013-02-28];HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0000508	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0020221	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0000007	PMID:22652185	PCS					I	HPO:probinson[2013-02-28];HPO:probinson[2020-07-22]
OMIM:610539	Gaucher disease, atypical		HP:0007334	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0001873	PMID:17919309	PCS		2/2			P	HPO:probinson[2013-02-28];HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0006897	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0001744	PMID:9930900;PMID:17919309	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0000666	PMID:9930900	PCS		1/1			P	HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0001336	PMID:9930900	PCS		1/1			P	HPO:probinson[2013-02-28];HPO:probinson[2021-09-22]
OMIM:610539	Gaucher disease, atypical		HP:0004975	PMID:17919309	PCS		1/2			P	HPO:probinson[2013-02-28];HPO:probinson[2021-09-22]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0001695	PMID:22422768	PCS		1/3			P	HPO:lccarmody[2018-06-29];HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0031273	PMID:22422768	PCS		1/3			P	HPO:lccarmody[2018-06-29];HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0011463	PMID:22422768	PCS		1/3			C	HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0006682	PMID:22422768	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0003593	PMID:22422768	PCS		2/3			C	HPO:probinson[2021-09-24];HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0000007	PMID:22422768	PCS					I	HPO:skoehler[2013-10-22]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0001657	PMID:22422768	PCS		0/3			P	HPO:lccarmody[2018-06-29];HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0003701	PMID:22422768	PCS		1/3			P	HPO:skoehler[2013-10-22];HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0031677	PMID:22422768	PCS		3/3			P	HPO:lccarmody[2018-06-29];HPO:probinson[2021-09-24]
OMIM:615441	Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness		HP:0001279	PMID:22422768	PCS		1/3			P	HPO:lccarmody[2018-06-29];HPO:probinson[2021-09-24]
DECIPHER:3	Williams-Beuren Syndrome (WBS)		HP:0001650	DECIPHER:3	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:3	Williams-Beuren Syndrome (WBS)		HP:0000232	DECIPHER:3	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:3	Williams-Beuren Syndrome (WBS)		HP:0004322	DECIPHER:3	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:3	Williams-Beuren Syndrome (WBS)		HP:0000691	DECIPHER:3	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:3	Williams-Beuren Syndrome (WBS)		HP:0000272	DECIPHER:3	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:3	Williams-Beuren Syndrome (WBS)		HP:0000736	DECIPHER:3	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:3	Williams-Beuren Syndrome (WBS)		HP:0001249	DECIPHER:3	IEA					P	HPO:skoehler[2013-05-29]
OMIM:613024	Follicular lymphoma, susceptibility to, 1		HP:0033125	PMID:2379110	PCS					P	HPO:probinson[2020-10-13]
OMIM:613024	Follicular lymphoma, susceptibility to, 1		HP:0010982	PMID:2379110	PCS					I	HPO:probinson[2020-10-13]
OMIM:102400	ACROOSTEOLYSIS		HP:0003621	OMIM:102400	TAS					C	HPO:probinson[2015-12-30]
OMIM:102400	ACROOSTEOLYSIS		HP:0009771	OMIM:102400	TAS					P	HPO:probinson[2015-12-30]
OMIM:102400	ACROOSTEOLYSIS		HP:0010177	OMIM:102400	TAS					P	HPO:probinson[2015-12-30]
OMIM:102400	ACROOSTEOLYSIS		HP:0000006	OMIM:102400	TAS					I	HPO:probinson[2015-12-30]
OMIM:175850	Porokeratosis plantaris, palmaris, et disseminata		HP:0100869	OMIM:175850	TAS					P	HPO:probinson[2012-06-10]
OMIM:175850	Porokeratosis plantaris, palmaris, et disseminata		HP:0200044	OMIM:175850	TAS					P	HPO:skoehler[2010-06-20]
OMIM:175850	Porokeratosis plantaris, palmaris, et disseminata		HP:0000006	OMIM:175850	TAS					I	HPO:probinson[2009-02-17]
OMIM:175850	Porokeratosis plantaris, palmaris, et disseminata		HP:0100870	OMIM:175850	TAS					P	HPO:probinson[2012-06-10]
OMIM:186700	Syringomyelia, isolated		HP:0003401	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0002650	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0002277	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0003487	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0002395	OMIM:186700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0003396	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0001260	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0002066	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0000020	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0002061	OMIM:186700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0003690	OMIM:186700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:186700	Syringomyelia, isolated		HP:0030833	OMIM:186700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:186700	Syringomyelia, isolated		HP:0012046	OMIM:186700	TAS					P	HPO:probinson[2012-08-01]
OMIM:186700	Syringomyelia, isolated		HP:0000639	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0007099	OMIM:186700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0002317	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0000006	OMIM:186700	IEA					I	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0005878	OMIM:186700	IEA					P	HPO:iea[2009-02-17]
OMIM:186700	Syringomyelia, isolated		HP:0002699	OMIM:186700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:106100	Angioedema, hereditary, 1		HP:0002960	OMIM:106100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:106100	Angioedema, hereditary, 1		HP:0002014	OMIM:106100	IEA					P	HPO:iea[2009-02-17]
OMIM:106100	Angioedema, hereditary, 1		HP:0003477	OMIM:106100	IEA		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0033748	PMID:17502473	PCS		1/1			P	HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0005225	OMIM:106100	IEA					P	HPO:iea[2009-02-17]
OMIM:106100	Angioedema, hereditary, 1		HP:0002013	OMIM:106100	IEA					P	HPO:iea[2009-02-17]
OMIM:106100	Angioedema, hereditary, 1		HP:0025434	PMID:17502473	PCS		1/1			P	HPO:probinson[2022-08-08]
OMIM:106100	Angioedema, hereditary, 1		HP:0011855	OMIM:106100	TAS					P	HPO:probinson[2012-07-21]
OMIM:106100	Angioedema, hereditary, 1		HP:0010783	OMIM:106100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:106100	Angioedema, hereditary, 1		HP:0034204	OMIM:106100	TAS					P	HPO:probinson[2022-04-15]
OMIM:106100	Angioedema, hereditary, 1		HP:0045042	PMID:17502473;PMID:16813612	PCS		3/3			P	HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0012027	PMID:16813612	PCS		1/2			P	HPO:probinson[2012-07-26];HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0100665	OMIM:106100	IEA					P	HPO:skoehler[2015-01-19]
OMIM:106100	Angioedema, hereditary, 1		HP:0011463	PMID:16813612	PCS		2/2			C	HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0100539	PMID:16813612	PCS		2/2			P	HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0011462	PMID:17502473	PCS		1/1			C	HPO:probinson[2022-08-08]
OMIM:106100	Angioedema, hereditary, 1		HP:0040078	PMID:17502473	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0000007	OMIM:106100	IEA					I	HPO:skoehler[2018-10-08]
OMIM:106100	Angioedema, hereditary, 1		HP:0001324	PMID:17502473	PCS		1/1			P	HPO:probinson[2022-03-31]
OMIM:106100	Angioedema, hereditary, 1		HP:0002027	OMIM:106100	IEA					P	HPO:iea[2009-02-17]
OMIM:106100	Angioedema, hereditary, 1		HP:0000006	PMID:3587308	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:608404	Platelet glycoprotein IV deficiency		HP:0001892	OMIM:608404	IEA					P	HPO:iea[2009-02-17]
OMIM:608404	Platelet glycoprotein IV deficiency		HP:0003010	OMIM:608404	TAS					P	HPO:iea[2009-02-17]
OMIM:608404	Platelet glycoprotein IV deficiency		HP:0000007	PMID:7686693	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-07-17]
OMIM:608404	Platelet glycoprotein IV deficiency		HP:0001902	OMIM:608404	IEA					P	HPO:iea[2009-02-17]
OMIM:608404	Platelet glycoprotein IV deficiency		HP:0001873	OMIM:608404	IEA					P	HPO:iea[2009-02-17]
OMIM:617524	Erythrokeratodermia variabilis et progressiva 2		HP:0003577	PMID:11017804	PCS		8/8			C	HPO:probinson[2023-06-04]
OMIM:617524	Erythrokeratodermia variabilis et progressiva 2		HP:0000998	OMIM:617524	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617524	Erythrokeratodermia variabilis et progressiva 2		HP:0200035	PMID:11017804	PCS		8/8			P	HPO:probinson[2023-06-04]
OMIM:617524	Erythrokeratodermia variabilis et progressiva 2		HP:0010783	PMID:11017804	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-04]
OMIM:617524	Erythrokeratodermia variabilis et progressiva 2		HP:0000982	PMID:11017804	PCS		0/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-04]
OMIM:617524	Erythrokeratodermia variabilis et progressiva 2		HP:0000006	PMID:11017804	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-04]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0001397	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0000486	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0000232	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0001596	OMIM:275630	IEA					P	HPO:skoehler[2010-06-20]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0001871	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0003198	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0001251	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0002240	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0000639	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0000407	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0008551	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0000007	OMIM:275630	IEA					I	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0000656	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0001324	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0007479	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0000523	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:275630	Chanarin-Dorfman syndrome		HP:0001249	OMIM:275630	IEA					P	HPO:iea[2009-02-17]
OMIM:621096	Immunodeficiency 132B		HP:0002586	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002783	PMID:39579173	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002582	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0025343	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0032235	PMID:35960817	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0040261	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0030812	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0100721	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0011463	PMID:39579173;PMID:35960817	PCS		11/12			C	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0100646	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0034189	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0001888	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0000999	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0001369	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0005425	PMID:35960817	PCS		7/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0025379	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002110	PMID:39579173;PMID:35960817	PCS		7/10			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0032564	PMID:39579173	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0033256	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0033583	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0034751	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0034156	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0000403	PMID:39579173;PMID:35960817	PCS		6/10			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0000246	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0003237	PMID:35960817	PCS		7/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0000006	PMID:35960817	PCS					I	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002028	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002840	PMID:35960817	PCS		3/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0410299	PMID:39579173;PMID:35960817	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0003212	PMID:35960817	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0034839	PMID:39579173;PMID:35960817	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0003496	PMID:35960817	PCS		4/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0025289	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0410295	PMID:35960817	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002240	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0410294	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0032261	PMID:35960817	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002716	PMID:39579173;PMID:35960817	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0006530	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0001744	PMID:39579173;PMID:35960817	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002633	PMID:35960817	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0410323	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0004313	PMID:39579173	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0003621	PMID:39579173	PCS		1/3			C	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0001047	PMID:35960817	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0003261	PMID:35960817	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0033555	PMID:35960817	PCS		3/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0011108	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0033559	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0033563	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002608	PMID:35960817	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0020136	PMID:35960817	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:621096	Immunodeficiency 132B		HP:0002205	PMID:39579173	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-27]
OMIM:601346	Martinez-Frias syndrome		HP:0002575	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0005235	OMIM:601346	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601346	Martinez-Frias syndrome		HP:0005245	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0002594	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0005233	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0005242	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0000007	OMIM:601346	IEA					I	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0001734	OMIM:601346	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601346	Martinez-Frias syndrome		HP:0001511	OMIM:601346	TAS					P	HPO:probinson[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0000047	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0002247	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:601346	Martinez-Frias syndrome		HP:0002566	OMIM:601346	IEA					P	HPO:iea[2009-02-17]
OMIM:182200	Sella turcica, bridged		HP:0000006	OMIM:182200	IEA					I	HPO:iea[2009-02-17]
OMIM:182200	Sella turcica, bridged		HP:0005449	OMIM:182200	IEA					P	HPO:iea[2009-02-17]
OMIM:619086	Deafness, autosomal dominant 79		HP:0001751	PMID:31972369	PCS		0/19			P	HPO:probinson[2020-12-15];HPO:probinson[2024-03-16]
OMIM:619086	Deafness, autosomal dominant 79		HP:0000408	PMID:31972369	PCS	HP:0003581	19/19			P	HPO:probinson[2020-12-15];HPO:probinson[2024-03-16]
OMIM:619086	Deafness, autosomal dominant 79		HP:0003581	PMID:31972369	PCS		19/19			C	HPO:probinson[2024-03-16]
OMIM:619086	Deafness, autosomal dominant 79		HP:0000006	PMID:31972369	PCS					I	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0001595	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000252	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0002664	OMIM:601811	IEA					P	HPO:skoehler[2010-06-18]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0001871	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0005280	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000819	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000939	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000518	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0001507	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000007	OMIM:601811	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0002669	OMIM:601811	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000311	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000377	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:601811	Premature aging syndrome, Okamoto type		HP:0000369	OMIM:601811	IEA					P	HPO:iea[2009-02-17]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0002960	OMIM:618398	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0003621	PMID:30374066	PCS		7/16			C	HPO:probinson[2022-11-04];HPO:probinson[2022-11-04]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0002155	OMIM:618398	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0003596	PMID:30374066	PCS		2/16			C	HPO:probinson[2022-11-04]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0000282	OMIM:618398	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0003584	PMID:30374066	PCS		2/16			C	HPO:probinson[2022-11-04]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0011900	OMIM:618398	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0034403	PMID:30374066	PCS		16/16			P	HPO:probinson[2022-12-18]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0003281	OMIM:618398	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0012156	OMIM:618398	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0001903	OMIM:618398	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0011463	PMID:30374066	PCS		1/16			C	HPO:probinson[2022-11-04]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0011462	PMID:30374066	PCS		4/16			C	HPO:probinson[2022-11-04]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0000007	PMID:30374066	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-04]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0001945	OMIM:618398	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0012490	PMID:30374066	PCS		16/16			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-04]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0001876	OMIM:618398	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618398	T-cell lymphoma, subcutaneous panniculitis-like		HP:0001744	OMIM:618398	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:620161	Congenital myopathy 15		HP:0001561	PMID:33755597	PCS		2/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0003577	PMID:33755597	PCS		4/4			C	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0001382	PMID:33755597	PCS		1/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0001252	PMID:33755597	PCS		2/4			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0012548	PMID:33755597	PCS		3/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0001270	PMID:33755597	PCS		3/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0030319	PMID:33755597	PCS		4/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0005180	PMID:33755597	PCS		1/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0012385	PMID:33755597	PCS		1/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0032341	PMID:33755597	PCS		3/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0000938	PMID:33755597	PCS		3/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0001558	PMID:33755597	PCS		1/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0001605	PMID:33755597	PCS		2/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0002515	PMID:33755597	PCS		2/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0003803	PMID:33755597	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0001324	PMID:33755597	PCS		4/4			P	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0000006	PMID:33755597	PCS					I	HPO:probinson[2023-03-25]
OMIM:620161	Congenital myopathy 15		HP:0003557	PMID:33755597	PCS		1/2			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:619938	Premature ovarian failure 20		HP:0000869	PMID:28541421	PCS		2/2			P	HPO:probinson[2022-08-06]
OMIM:619938	Premature ovarian failure 20		HP:0011969	PMID:28541421	PCS		2/2			P	HPO:probinson[2022-08-06]
OMIM:619938	Premature ovarian failure 20		HP:0008222	PMID:28541421	PCS		2/2			P	HPO:probinson[2022-08-06]
OMIM:619938	Premature ovarian failure 20		HP:0011462	PMID:28541421	PCS		2/2			C	HPO:probinson[2022-08-06]
OMIM:619938	Premature ovarian failure 20		HP:0008232	PMID:28541421	PCS		2/2			P	HPO:probinson[2022-08-06]
OMIM:619938	Premature ovarian failure 20		HP:0000007	PMID:28541421	PCS					I	HPO:probinson[2022-08-06]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0002540	PMID:27094857	PCS		2/4			P	HPO:skoehler[2018-10-08]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0000750	PMID:27094857	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0011968	PMID:27094857	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0001272	PMID:27094857	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0002066	PMID:27094857	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0000490	PMID:27094857	PCS		1/4			P	HPO:skoehler[2019-04-18]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0001252	PMID:27094857	PCS		4/4			P	HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0001263	PMID:27094857	PCS		4/4			P	HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0001251	PMID:27094857	PCS		4/4			P	HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0003593	PMID:27094857	PCS		4/4			C	HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0001270	PMID:27094857	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0006297	PMID:27094857	PCS		4/4			P	HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0000218	PMID:27094857	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0025336	PMID:27094857	PCS		3/4			P	HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0002007	PMID:27094857	PCS		1/4			P	HPO:skoehler[2018-10-08]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0000278	PMID:27094857	PCS		1/4			P	HPO:skoehler[2018-10-08]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0001249	PMID:27094857	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0000006	PMID:27094857	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-22]
OMIM:617915	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome		HP:0003557	PMID:27094857	PCS		2/4			P	HPO:probinson[2023-03-22]
OMIM:125530	Dermal ridges, nelson syndrome		HP:0007477	OMIM:125530	TAS					P	HPO:probinson[2017-06-14]
OMIM:125530	Dermal ridges, nelson syndrome		HP:0000006	OMIM:125530	TAS					I	HPO:probinson[2009-02-17]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0000365	OMIM:256200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0000100	OMIM:256200	IEA					P	HPO:iea[2009-02-17]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0009650	OMIM:256200	TAS					P	HPO:probinson[2012-06-10]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0000193	OMIM:256200	IEA					P	HPO:iea[2009-02-17]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0010097	OMIM:256200	TAS					P	HPO:probinson[2012-06-10]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0010103	OMIM:256200	TAS					P	HPO:probinson[2012-06-10]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0000007	OMIM:256200	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0009611	OMIM:256200	TAS					P	HPO:probinson[2012-06-10]
OMIM:256200	Nephrosis with deafness and urinary tract and digital malformations		HP:0001423	OMIM:256200	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:103285	Adult syndrome		HP:0001770	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0002286	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0002561	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0001171	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000958	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000579	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0001803	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0002557	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0006357	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0006610	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000677	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0002215	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000992	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0004334	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0003187	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0001480	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000691	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0002293	OMIM:103285	TAS					P	HPO:skoehler[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000968	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000509	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0001839	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000668	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0002209	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000964	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0007455	OMIM:103285	IEA					P	HPO:skoehler[2012-10-11]
OMIM:103285	Adult syndrome		HP:0000202	OMIM:103285	IEA					P	HPO:skoehler[2012-10-11]
OMIM:103285	Adult syndrome		HP:0000006	OMIM:103285	IEA					I	HPO:iea[2009-02-17]
OMIM:103285	Adult syndrome		HP:0000963	OMIM:103285	IEA					P	HPO:iea[2009-02-17]
OMIM:123155	Craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus		HP:0001320	OMIM:123155	TAS					P	HPO:skoehler[2009-02-17]
OMIM:123155	Craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus		HP:0007291	OMIM:123155	TAS					P	HPO:skoehler[2009-02-17]
OMIM:123155	Craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus		HP:0004442	OMIM:123155	TAS					P	HPO:skoehler[2009-02-17]
OMIM:123155	Craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus		HP:0000238	OMIM:123155	TAS					P	HPO:skoehler[2009-02-17]
OMIM:123155	Craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus		HP:0001305	OMIM:123155	TAS					P	HPO:skoehler[2009-02-17]
OMIM:123155	Craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus		HP:0000006	OMIM:123155	TAS					I	HPO:skoehler[2009-02-17]
OMIM:128000	DYSTELEPHALANGY		HP:0004226	OMIM:128000	TAS					P	HPO:probinson[2012-07-17]
OMIM:128000	DYSTELEPHALANGY		HP:0000006	OMIM:128000	IEA					I	HPO:iea[2009-02-17]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001276	PMID:32738225	PCS		4/7			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000582	PMID:32738225	PCS		4/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0003577	PMID:32738225	PCS		8/8			C	HPO:probinson[2022-03-17]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0002265	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0002066	PMID:32738225	PCS		4/7			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001251	PMID:32738225	PCS		7/7			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0032794	PMID:32738225	PCS		2/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001290	PMID:32738225	PCS		3/7			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0012444	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0012766	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000316	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000337	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000733	PMID:32738225	PCS		2/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0025336	PMID:32738225	PCS		5/6			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0030084	PMID:32738225	PCS		2/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000278	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001249	PMID:32738225	PCS		8/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001347	PMID:32738225	PCS		4/7			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001166	PMID:32738225	PCS		2/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000396	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001265	PMID:32738225	PCS		3/7			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000252	PMID:32738225	PCS		6/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000750	PMID:32738225	PCS		8/8		HP:0012828	P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0031936	PMID:32738225	PCS		7/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001761	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001263	PMID:32738225	PCS		8/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0010830	PMID:32738225	PCS		2/4			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0025190	PMID:32738225	PCS		5/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0009830	PMID:32738225	PCS		3/5			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000767	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0002942	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001159	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0007359	PMID:32738225	PCS		3/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000006	PMID:32738225	PCS					I	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000369	PMID:32738225	PCS		2/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001337	PMID:32738225	PCS		2/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0000687	PMID:32738225	PCS		2/8			P	HPO:probinson[2020-12-22]
OMIM:619092	Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant		HP:0001336	PMID:32738225	PCS		1/8			P	HPO:probinson[2020-12-22]
OMIM:161400	Narcolepsy 1		HP:5200356	PMID:36592569	PCS		24/39			P	HPO:probinson[2025-10-20]
OMIM:161400	Narcolepsy 1		HP:0002494	PMID:10973318	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:161400	Narcolepsy 1		HP:0002519	PMID:10973318	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:161400	Narcolepsy 1		HP:0001262	PMID:10973318	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:161400	Narcolepsy 1		HP:0025233	PMID:10973318;PMID:36592569	PCS		31/40			P	HPO:probinson[2025-10-20];HPO:probinson[2022-09-02]
OMIM:161400	Narcolepsy 1		HP:0003593	PMID:10973318	PCS		1/1			C	HPO:probinson[2022-09-02]
OMIM:161400	Narcolepsy 1		HP:0006896	OMIM:161400	IEA					P	HPO:iea[2009-02-17]
OMIM:161400	Narcolepsy 1		HP:0002524	PMID:10973318;PMID:36592569	PCS		39/40			P	HPO:probinson[2025-10-20];HPO:probinson[2012-04-11];HPO:probinson[2022-09-02]
OMIM:161400	Narcolepsy 1		HP:0030050	PMID:10973318	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-02]
OMIM:161400	Narcolepsy 1		HP:0000006	PMID:10973318	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:300046	Intellectual developmental disorder, X-linked 23		HP:0001419	OMIM:300046	TAS					I	HPO:probinson[2012-07-17]
OMIM:300046	Intellectual developmental disorder, X-linked 23		HP:0001249	OMIM:300046	TAS					P	HPO:probinson[2009-02-17]
OMIM:616389	Night blindness, congenital stationary, type 1G		HP:0001133	PMID:26472407	PCS		1/1			P	HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:616389	Night blindness, congenital stationary, type 1G		HP:0000007	PMID:22190596	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616389	Night blindness, congenital stationary, type 1G		HP:0007642	PMID:22190596	PCS	HP:0011463	4/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616389	Night blindness, congenital stationary, type 1G		HP:0007642	PMID:26472407	PCS		1/1			P	HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:616389	Night blindness, congenital stationary, type 1G		HP:0000505	PMID:22190596	PCS		0/4			P	HPO:probinson[2022-04-12]
OMIM:616389	Night blindness, congenital stationary, type 1G		HP:0000543	PMID:26472407	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-12]
OMIM:616389	Night blindness, congenital stationary, type 1G		HP:0000510	PMID:26472407	PCS		1/1			P	HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520kb		HP:0000708	PMID:22970919	PCS		9/16			P	HPO:skoehler[2013-01-10];HPO:probinson[2023-07-08]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520-kbfragile site 16p12, included		HP:0000252	PMID:22970919	PCS		7/20			P	HPO:probinson[2023-07-08]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520kb		HP:0000750	PMID:22970919	PCS		15/15			P	HPO:skoehler[2013-01-10];HPO:probinson[2023-07-08]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520kb		HP:0001250	PMID:22970919	PCS		8/22			P	HPO:skoehler[2013-01-10];HPO:probinson[2023-07-08]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520kb		HP:0001263	PMID:22970919	PCS		42/42			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-07-08]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520-kbfragile site 16p12, included		HP:0001252	PMID:22970919	PCS		10/21			P	HPO:probinson[2023-07-08]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520kb		HP:0001999	OMIM:136570	IEA		HP:0040281			P	HPO:skoehler[2013-01-10]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520-kbfragile site 16p12, included		HP:0004383	PMID:22970919	PCS		4/21			P	HPO:probinson[2023-07-08]
OMIM:136570	Chromosome 16p12.1 deletion syndrome, 520-kbfragile site 16p12, included		HP:0001510	PMID:22970919	PCS		9/22			P	HPO:probinson[2023-07-08]
OMIM:113900	Progressive familial heart block, type IA		HP:0011711	PMID:10471492	PCS		3/15			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-16]
OMIM:113900	Progressive familial heart block, type IA		HP:0002094	OMIM:113900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:113900	Progressive familial heart block, type IA		HP:0011712	PMID:10471492	PCS		5/15			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-16]
OMIM:113900	Progressive familial heart block, type IA		HP:0005172	PMID:10471492	PCS		3/15			P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-16]
OMIM:113900	Progressive familial heart block, type IA		HP:0005170	OMIM:113900	PCS					P	HPO:probinson[2012-04-11]
OMIM:113900	Progressive familial heart block, type IA		HP:0001279	PMID:10471492	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2022-07-16]
OMIM:113900	Progressive familial heart block, type IA		HP:0000006	PMID:10471492	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-07-16]
OMIM:113900	Progressive familial heart block, type IA		HP:0001645	OMIM:113900	PCS					P	HPO:probinson[2012-04-11]
OMIM:113900	Progressive familial heart block, type IA		HP:0012248	PMID:10471492	PCS		8/15			P	HPO:probinson[2022-07-16]
OMIM:113900	Progressive familial heart block, type IA		HP:0001699	OMIM:113900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606824	Glucose/galactose malabsorption		HP:0002024	OMIM:606824	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606824	Glucose/galactose malabsorption		HP:0001508	OMIM:606824	TAS					P	HPO:probinson[2009-02-17]
OMIM:606824	Glucose/galactose malabsorption		HP:0003076	OMIM:606824	TAS					P	HPO:probinson[2009-02-17]
OMIM:606824	Glucose/galactose malabsorption		HP:0030143	OMIM:606824	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606824	Glucose/galactose malabsorption		HP:0000007	PMID:2008213	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-10-22]
OMIM:606824	Glucose/galactose malabsorption		HP:0004924	OMIM:606824	TAS					P	HPO:probinson[2009-02-17]
OMIM:606824	Glucose/galactose malabsorption		HP:0003270	OMIM:606824	TAS					P	HPO:skoehler[2013-10-06]
OMIM:606824	Glucose/galactose malabsorption		HP:0001942	OMIM:606824	TAS					P	HPO:probinson[2009-02-17]
OMIM:606824	Glucose/galactose malabsorption		HP:0001986	PMID:2008213	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-22]
OMIM:606824	Glucose/galactose malabsorption		HP:0002028	PMID:2008213	PCS		2/2			P	HPO:probinson[2012-07-19];HPO:probinson[2022-10-22]
OMIM:606824	Glucose/galactose malabsorption		HP:0003623	PMID:2008213	PCS		2/2			C	HPO:probinson[2022-10-22]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0002521	PMID:29394991	PCS	HP:0003593	3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0002510	PMID:29394991	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0002540	PMID:29394991	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0001250	PMID:29394991	PCS	HP:0003593	3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0002384	PMID:29394991	PCS		2/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0002283	PMID:29394991	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0001263	PMID:29394991	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0003593	PMID:29394991	PCS		3/3			C	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0032794	PMID:29394991	PCS		2/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0010851	PMID:29394991	PCS	HP:0003593	1/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0011097	PMID:29394991	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0034396	PMID:29394991	PCS		3/3			P	HPO:probinson[2022-12-18]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0032792	PMID:29394991	PCS		1/3			P	HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0000007	PMID:29394991	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-05]
OMIM:617929	Epileptic encephalopathy, early infantile, 60		HP:0200134	PMID:29394991	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-05]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000341	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0002421	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0010804	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0002121	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0001252	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0003593	PMID:35293990	PCS		2/2			C	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0032799	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0031491	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000639	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0100704	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0007021	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000218	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0008936	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0003763	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000252	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0001344	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0002870	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0002079	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0002310	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0011968	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0002072	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0012736	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0011327	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000508	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000007	PMID:35293990	PCS					I	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000400	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0200055	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0001257	PMID:35293990	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620149	Developmental and epileptic encephalopathy 110		HP:0000369	PMID:35293990	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001166	PMID:35358416	PCS		2/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0003577	PMID:35358416	PCS		1/12			C	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0002650	PMID:35358416	PCS		2/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001684	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001250	PMID:35358416	PCS		4/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001263	PMID:35358416	PCS		12/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001252	PMID:35358416	PCS		2/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0003593	PMID:35358416	PCS		10/12			C	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0033522	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0008070	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0012469	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0011463	PMID:35358416	PCS		1/12			C	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0000729	PMID:35358416	PCS		5/10			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001669	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0002616	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0000767	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0004209	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0000768	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001863	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001357	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0000006	PMID:35358416	PCS					I	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0001249	PMID:35358416	PCS		12/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0000369	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:619910	Intellectual developmental disorder, autosomal dominant 66		HP:0000248	PMID:35358416	PCS		1/12			P	HPO:probinson[2022-08-17]
OMIM:601187	Gurrieri syndrome		HP:0002652	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0002750	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0004322	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0001250	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0003274	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0000007	OMIM:601187	IEA					I	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0005638	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0002866	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:601187	Gurrieri syndrome		HP:0001249	OMIM:601187	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0001100	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0002211	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0001271	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0001263	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0001252	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0002251	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0001251	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0001053	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0000639	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0000407	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0000635	OMIM:277580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277580	Waardenburg-Shah syndrome		HP:0000007	OMIM:277580	IEA					I	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0002216	OMIM:277580	IEA					P	HPO:skoehler[2010-06-18]
OMIM:277580	Waardenburg-Shah syndrome		HP:0002227	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0002415	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0000006	OMIM:277580	IEA					I	HPO:skoehler[2010-06-19]
OMIM:277580	Waardenburg-Shah syndrome		HP:0002313	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:277580	Waardenburg-Shah syndrome		HP:0002226	OMIM:277580	IEA					P	HPO:iea[2009-02-17]
OMIM:617068	Portal hypertension, noncirrhotic		HP:0001409	PMID:26874653	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-20]
OMIM:617068	Portal hypertension, noncirrhotic		HP:0002240	PMID:26874653	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-20]
OMIM:617068	Portal hypertension, noncirrhotic		HP:0000007	PMID:26874653	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-20]
OMIM:617068	Portal hypertension, noncirrhotic		HP:0002040	PMID:26874653	PCS		7/8			P	HPO:probinson[2021-10-20]
OMIM:617068	Portal hypertension, noncirrhotic		HP:0002910	PMID:26874653	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-20]
OMIM:617068	Portal hypertension, noncirrhotic		HP:0001744	PMID:26874653	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-20]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0000871	OMIM:262600	IEA					P	HPO:iea[2009-02-17]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0004322	OMIM:262600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0001250	OMIM:262600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0030344	PMID:9462743	PCS		4/4			P	HPO:probinson[2023-02-18]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0002173	OMIM:262600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0030341	PMID:9462743	PCS		6/6			P	HPO:probinson[2023-02-18]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0034323	PMID:9462743	PCS		6/6			P	HPO:probinson[2023-02-18]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0031098	PMID:9462743	PCS		6/6			P	HPO:probinson[2023-02-18]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0011043	PMID:9462743	PCS		0/4			P	HPO:probinson[2023-02-18]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0008202	PMID:9462743	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-18]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0000007	PMID:9462743	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0000821	OMIM:262600	IEA					P	HPO:iea[2009-02-17]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0001998	OMIM:262600	IEA					P	HPO:iea[2009-02-17]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0000846	OMIM:262600	IEA					P	HPO:iea[2009-02-17]
OMIM:262600	Pituitary hormone deficiency, combined, 2		HP:0000135	OMIM:262600	IEA					P	HPO:iea[2009-02-17]
OMIM:609256	Myopia 7		HP:0001426	PMID:15307048	PCS					I	HPO:probinson[2022-09-12]
OMIM:609256	Myopia 7		HP:0000545	PMID:15307048	PCS					P	HPO:skoehler[2014-10-17];HPO:probinson[2022-09-12]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0002301	PMID:27571260	PCS		2/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0003676	PMID:27571260	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0003621	PMID:27571260	PCS		8/37			C	HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0003596	PMID:27571260	PCS		2/37			C	HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001332	PMID:27571260	PCS		4/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001288	PMID:27571260	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001250	PMID:27571260	PCS		16/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001260	PMID:27571260	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0002352	PMID:27571260	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001263	PMID:27571260	PCS		20/40			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001251	PMID:27571260	PCS		5/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0003593	PMID:27571260	PCS		19/37			C	HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0002071	PMID:27571260	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0011463	PMID:27571260	PCS		7/37			C	HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0011462	PMID:27571260	PCS		1/37			C	HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0000007	PMID:27571260	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0007256	PMID:27571260	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001268	PMID:27571260	PCS		8/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0002514	PMID:27571260	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0002415	PMID:27571260	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001257	PMID:27571260	PCS		6/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:614561	Leukoencephalopathy, brain calcifications, and cysts		HP:0001337	PMID:27571260	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0003621	PMID:11208676	PCS		1/4			C	HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0001250	PMID:17875969	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0025478	PMID:17875969	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0011704	PMID:17875969	PCS		1/6			P	HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0034039	PMID:11208676	PCS		1/4			P	HPO:probinson[2021-10-03]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0034040	PMID:11208676	PCS		4/4		HP:0025377	P	HPO:probinson[2021-10-03]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0011463	PMID:11208676	PCS		2/4			C	HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0011462	PMID:11208676	PCS		1/4			C	HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0006673	PMID:17875969	PCS		3/6			P	HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0004758	PMID:17875969	PCS		5/6			P	HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0001279	PMID:11208676	PCS		8/9		HP:0025377	P	HPO:probinson[2021-09-25];HPO:skoehler[2012-10-17];HPO:probinson[2021-07-17]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0004757	PMID:17875969	PCS		2/6			P	HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0000006	PMID:11208676	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-17]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0004756	PMID:11208676	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-07-17]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0001645	PMID:17875969;PMID:11208676	PCS		12/16			P	HPO:probinson[2021-07-17];HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0001678	PMID:17875969	PCS		1/6			P	HPO:probinson[2021-09-25]
OMIM:604772	Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy		HP:0001644	PMID:17875969	PCS		2/6			P	HPO:probinson[2021-09-25]
DECIPHER:65	Atr-16 syndrome		HP:0001877	DECIPHER:65	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:65	Atr-16 syndrome		HP:0001249	DECIPHER:65	IEA					P	HPO:skoehler[2013-05-29]
OMIM:115430	Carpal tunnel syndrome		HP:0012276	OMIM:115430	TAS					P	HPO:probinson[2013-04-07]
OMIM:115430	Carpal tunnel syndrome		HP:0012185	OMIM:115430	TAS					P	HPO:skoehler[2013-02-25]
OMIM:115430	Carpal tunnel syndrome		HP:0009830	OMIM:115430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:115430	Carpal tunnel syndrome		HP:0008326	OMIM:115430	IEA					P	HPO:iea[2009-02-17]
OMIM:115430	Carpal tunnel syndrome		HP:0000006	OMIM:115430	IEA					I	HPO:iea[2009-02-17]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002069	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002025	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0010804	PMID:23561847	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0003577	PMID:23561847	PCS		1/2			C	HPO:skoehler[2013-06-04]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000486	PMID:23561846	PCS		2/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002540	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0004322	PMID:23561846	PCS		1/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001250	PMID:23561847	PCS		2/2			P	HPO:skoehler[2013-06-04];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002121	PMID:23561846	PCS		1/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0003155	PMID:23561847	PCS		2/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0003196	PMID:23561847	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0006829	PMID:23561846	PCS		1/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001252	PMID:23561846;PMID:23561847	PCS		4/5			P	HPO:probinson[2023-04-05];HPO:skoehler[2014-11-26];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0003593	PMID:23561847	PCS		1/2			C	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0032794	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001270	PMID:23561846	PCS		3/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0012444	PMID:23561846	PCS		1/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0008398	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000316	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001305	PMID:23561846	PCS		1/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000637	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001324	PMID:23561846	PCS		2/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000455	PMID:23561847	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0006118	PMID:23561847	PCS		2/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000154	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000252	PMID:23561846	PCS		1/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000175	PMID:23561847	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000431	PMID:23561847	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002650	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000750	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001344	PMID:23561847	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002079	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002373	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001263	PMID:23561847	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0002251	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000407	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001558	PMID:23561846	PCS		1/3			P	HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0000007	PMID:23561846	PCS					I	HPO:skoehler[2013-06-04];HPO:probinson[2023-04-05]
OMIM:614207	Hyperphosphatasia with impaired intellectual development syndrome 3		HP:0001631	PMID:23561847	PCS		1/2			P	HPO:probinson[2023-04-05]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0001397	OMIM:615119	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0001298	OMIM:615119	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0000252	OMIM:615119	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0011968	PMID:15235026	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0001252	OMIM:615119	TAS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0003593	PMID:15235026	PCS		1/1			C	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0002061	PMID:15235026	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0002171	OMIM:615119	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0011800	PMID:12474143	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0025085	PMID:15235026	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0033044	PMID:15235026	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0001639	PMID:12474143	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0001558	OMIM:615119	TAS					P	HPO:skoehler[2013-05-03]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0007146	PMID:15235026	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0000007	PMID:12474143	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0001638	OMIM:615119	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0000488	PMID:15235026	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0000666	PMID:15235026	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0003623	PMID:12474143	PCS		1/1			C	HPO:probinson[2023-03-04]
OMIM:615119	Mitochondrial complex IV deficiency, nuclear type 6		HP:0003128	PMID:12474143	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:616410	Spinocerebellar ataxia 41		HP:0003676	OMIM:616410	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616410	Spinocerebellar ataxia 41		HP:0001272	OMIM:616410	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616410	Spinocerebellar ataxia 41		HP:0002066	PMID:25477146	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:616410	Spinocerebellar ataxia 41		HP:0003581	PMID:25477146	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-07]
OMIM:616410	Spinocerebellar ataxia 41		HP:0001251	OMIM:616410	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616410	Spinocerebellar ataxia 41		HP:0002172	PMID:25477146	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:616410	Spinocerebellar ataxia 41		HP:0002317	PMID:25477146	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-11-07]
OMIM:616410	Spinocerebellar ataxia 41		HP:0000006	PMID:25477146	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-07]
OMIM:616410	Spinocerebellar ataxia 41		HP:0006855	PMID:25477146	PCS	HP:0003581	1/1			P	HPO:probinson[2022-11-07]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0100303	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0003236	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0003555	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0000759	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0003551	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0003581	OMIM:609524	IEA					C	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0002515	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0002093	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0003715	OMIM:609524	IEA					P	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0003701	OMIM:609524	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0000006	OMIM:609524	IEA					I	HPO:iea[2009-02-17]
OMIM:609524	Filaminopathy, autosomal dominant		HP:0003677	OMIM:609524	IEA					C	HPO:iea[2009-02-17]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0008529	PMID:34715011	PCS		3/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000286	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001276	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0033748	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0006989	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001250	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0030891	PMID:34715011	PCS		2/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0003074	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0032653	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0012377	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000815	PMID:34715011	PCS		3/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0012074	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0007340	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000316	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001649	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0004418	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0002315	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001269	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001249	PMID:34715011	PCS		3/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0003326	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0002650	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000233	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0002354	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0002076	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0011968	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0002197	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0002495	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0002151	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001263	PMID:34715011	PCS		4/8			P	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001284	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0005484	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0032388	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0011344	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000709	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0100654	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000308	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000407	PMID:34715011	PCS		2/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000729	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000007	PMID:34715011	PCS					I	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000543	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001511	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001513	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0001337	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0025406	PMID:34715011	PCS		1/8			P	HPO:probinson[2022-04-30]
OMIM:619737	Combined oxidative phosphorylation deficiency 54		HP:0000786	PMID:34715011	PCS		3/8			P	HPO:probinson[2022-04-30]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000365	PMID:9875048	PCS		20/24			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000122	PMID:4436358	PCS		7/45			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0002162	OMIM:118100	TAS		HP:0040282			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0030680	PMID:4436358;PMID:5645110	PCS		21/505			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000912	PMID:4436358	PCS		21/50			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0002813	PMID:18425797;PMID:16585825	PCS	HP:0003577	HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000410	PMID:9875048	PCS		5/24			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0005988	PMID:4436358	PCS					P	HPO:probinson[2012-04-24];HPO:probinson[2022-09-02]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000077	PMID:4436358	PCS		16/45			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000175	PMID:4436358	PCS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0030325	PMID:11950676	PCS					P	HPO:probinson[2015-04-19]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0002650	PMID:4436358	PCS		30/50			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000772	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0005640	PMID:18425797	PCS	HP:0003577	HP:0040281			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000470	PMID:1739048	PCS		HP:0040281			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0007291	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000407	PMID:9875048	PCS		8/24			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000707	PMID:9702666	PCS		5/19			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000405	PMID:9875048	PCS		5/24			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000466	PMID:1739048	PCS		HP:0040281			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0001335	PMID:4436358	PCS		9/50			P	HPO:probinson[2012-04-24]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000465	PMID:4436358	PCS					P	HPO:probinson[2012-04-24];HPO:probinson[2022-09-02]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000006	PMID:18425797	PCS					I	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0004602	PMID:18425797	PCS		HP:0040281			P	HPO:probinson[2009-02-17]
OMIM:118100	Klippel-Feil syndrome 1, autosomal dominant		HP:0000324	PMID:4436358	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-02]
OMIM:618429	Spermatogenic failure 37		HP:0033393	PMID:30929735	PCS		3/3			P	HPO:probinson[2022-11-06]
OMIM:618429	Spermatogenic failure 37		HP:0032560	PMID:30929735	PCS		3/3			P	HPO:probinson[2022-11-06]
OMIM:618429	Spermatogenic failure 37		HP:0003251	PMID:30929735	PCS		3/3			P	HPO:probinson[2022-11-06]
OMIM:618429	Spermatogenic failure 37		HP:0011462	PMID:30929735	PCS		3/3			C	HPO:probinson[2022-11-06]
OMIM:618429	Spermatogenic failure 37		HP:0000007	PMID:30929735	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-06]
OMIM:618429	Spermatogenic failure 37		HP:0012207	PMID:30929735	PCS		3/3			P	HPO:probinson[2022-11-06]
OMIM:618429	Spermatogenic failure 37		HP:0032558	PMID:30929735	PCS		3/3			P	HPO:probinson[2022-11-06]
OMIM:618429	Spermatogenic failure 37		HP:0032559	PMID:30929735	PCS		3/3			P	HPO:probinson[2022-11-06]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0001265	PMID:21820098	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0003676	PMID:21820098	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0003621	PMID:21820098	PCS		7/8			C	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0033748	PMID:21820098	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0003577	PMID:21820098	PCS		1/8			C	HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0006858	PMID:21820098	PCS		6/8			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0004322	PMID:21820098	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0001263	PMID:21820098	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0009053	PMID:21820098	PCS		8/8			P	HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0007460	PMID:21820098	PCS		7/8			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0006121	PMID:21820098	PCS		8/8			P	HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0009830	OMIM:614213	IEA					P	HPO:skoehler[2015-01-27]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0009027	PMID:21820098	PCS		4/4			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0000007	PMID:21820098	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0008954	PMID:21820098	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0006886	PMID:21820098	PCS		6/8			P	HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0002522	PMID:21820098	PCS		2/3			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:614213	Neuropathy, hereditary sensory, type IIC		HP:0001249	PMID:21820098	PCS		1/8			P	HPO:probinson[2022-12-04]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0003015	PMID:24290375	PCS		3/4			P	HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0003577	PMID:24290375	PCS		4/4			C	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0004467	PMID:24290375	PCS		2/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000882	PMID:24290375	PCS		1/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0008905	PMID:24290375	PCS		4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0004322	PMID:24290375	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000160	PMID:24290375	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0003375	PMID:24290375	PCS		4/4			P	HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0005792	PMID:24290375	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0002938	PMID:24290375	PCS		2/4			P	HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0006595	PMID:24290375	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000218	PMID:24290375	PCS		2/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000413	PMID:24290375	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0001249	PMID:24290375	PCS		0/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0020206	PMID:24290375	PCS		4/4			P	HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000494	PMID:24290375	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000252	PMID:24290375	PCS		2/4			P	HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0001762	PMID:24290375	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0011968	PMID:24290375	PCS		3/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0003022	PMID:24290375	PCS		2/4			P	HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000490	OMIM:602471	IEA					P	HPO:iea[2009-02-17]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000272	PMID:24290375	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0003083	PMID:24290375	PCS		2/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0034392	PMID:24290375	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0002827	PMID:24290375	PCS		4/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0008785	PMID:24290375	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000007	PMID:24290375	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000601	OMIM:602471	IEA					P	HPO:iea[2009-02-17]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000405	PMID:24290375	PCS		4/4			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000028	PMID:24290375	PCS		2/2	MALE		P	HPO:skoehler[2014-04-13];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0000347	PMID:24290375	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:602471	Short stature, auditory canal atresia, mandibular hypoplasia, andskeletal abnormalities		HP:0002643	PMID:24290375	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0001056	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0003577	PMID:10484780;PMID:7545057	PCS		2/2			C	HPO:probinson[2022-05-12]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0001561	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0004399	PMID:7545057	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0004399	PMID:9792864	IEA	HP:0003577	4/5			P	HPO:probinson[2021-06-23]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0004399	PMID:10484780	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0002032	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0001030	OMIM:226730	IEA					P	HPO:skoehler[2010-06-20]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0002164	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0003341	PMID:10484780;PMID:7545057	PCS		2/2			P	HPO:probinson[2022-05-12];HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0002041	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0001075	OMIM:226730	TAS					P	HPO:probinson[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0034378	PMID:10484780	PCS	HP:0003577	1/1			P	HPO:probinson[2022-09-05]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0001060	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0011432	OMIM:226730	TAS					H	HPO:probinson[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0008066	PMID:10484780	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0006297	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0002804	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0000007	PMID:7545057	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0000656	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0007589	PMID:7545057	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0001522	PMID:7545057	PCS		2/2			C	HPO:probinson[2022-05-12];HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0008404	OMIM:226730	TAS					P	HPO:skoehler[2013-05-03]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0200097	PMID:7545057	PCS		1/1			P	HPO:probinson[2021-06-23];HPO:probinson[2022-05-12]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0001798	OMIM:226730	IEA					P	HPO:iea[2009-02-17]
OMIM:226730	Epidermolysis bullosa, junctional, with pyloric atresia		HP:0020117	PMID:9792864	PCS		3/3			P	HPO:probinson[2021-06-23]
OMIM:155000	Maxillofacial dysostosis		HP:0000494	OMIM:155000	IEA					P	HPO:iea[2009-02-17]
OMIM:155000	Maxillofacial dysostosis		HP:0000750	OMIM:155000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:155000	Maxillofacial dysostosis		HP:0000377	OMIM:155000	IEA					P	HPO:iea[2009-02-17]
OMIM:155000	Maxillofacial dysostosis		HP:0000006	OMIM:155000	IEA					I	HPO:iea[2009-02-17]
OMIM:155000	Maxillofacial dysostosis		HP:0000303	OMIM:155000	IEA					P	HPO:iea[2009-02-17]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0000640	PMID:21950986	PCS		27/27			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0000364	PMID:21950986	PCS		0/27			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0001272	PMID:21950986	PCS		22/27			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0001151	OMIM:614575	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0002066	PMID:30926972;PMID:21950986	PCS		39/39			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0001251	PMID:30926972	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0001152	PMID:21950986	PCS		27/27			P	HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0010545	PMID:30926972	PCS		5/11			P	HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0012332	PMID:30926972	PCS		12/56			P	HPO:probinson[2021-02-13]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0000639	PMID:30926972	PCS		7/12			P	HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0003447	PMID:21950986	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0006855	PMID:30926972	PCS		9/10			P	HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0007328	PMID:21950986	PCS		21/27			P	HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0001265	PMID:30926972	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0002494	PMID:30926972	PCS		2/5			P	HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0001260	PMID:30926972;PMID:21950986	PCS		37/40			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0002495	PMID:21950986	PCS		21/27			P	HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0003581	PMID:32851396;PMID:21950986	PCS		40/40			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-20];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0012735	PMID:30926972	PCS		29/66			P	HPO:probinson[2021-02-13];HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0002172	OMIM:614575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0002070	PMID:30926972;PMID:21950986	PCS		36/38			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20];HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0007230	PMID:30926972	PCS		8/8			P	HPO:probinson[2022-07-20]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0009830	PMID:30926972	PCS		56/56			P	HPO:probinson[2021-02-13]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0000007	PMID:30926972	TAS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-13]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0002403	OMIM:614575	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0003438	PMID:21950986	PCS		15/27			P	HPO:probinson[2024-03-15]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0008568	PMID:30926972	PCS		30/56			P	HPO:skoehler[2015-07-29];HPO:probinson[2021-02-13]
OMIM:614575	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome		HP:0003677	PMID:21950986	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-15]
OMIM:610713	Brachydactyly-Syndactyly syndrome		HP:0012385	PMID:23995701	PCS					P	HPO:probinson[2017-06-23]
OMIM:610713	Brachydactyly-Syndactyly syndrome		HP:0012165	PMID:23995701	PCS					P	HPO:probinson[2017-06-23]
OMIM:610713	Brachydactyly-Syndactyly syndrome		HP:0001156	PMID:23995701	PCS					P	HPO:probinson[2017-06-23]
OMIM:610713	Brachydactyly-Syndactyly syndrome		HP:0011927	PMID:23995701	PCS					P	HPO:probinson[2017-06-23]
OMIM:610713	Brachydactyly-Syndactyly syndrome		HP:0006101	PMID:23995701	PCS					P	HPO:probinson[2017-06-23]
OMIM:610713	Brachydactyly-Syndactyly syndrome		HP:0001159	PMID:23995701	PCS					P	HPO:probinson[2017-06-23]
OMIM:610713	Brachydactyly-Syndactyly syndrome		HP:0009803	PMID:23995701	PCS					P	HPO:probinson[2017-06-23]
OMIM:300085	Cone-Rod dystrophy, X-linked, 2		HP:0008020	OMIM:300085	TAS					P	HPO:probinson[2009-02-17]
OMIM:300085	Cone-Rod dystrophy, X-linked, 2		HP:0000548	OMIM:300085	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300085	Cone-Rod dystrophy, X-linked, 2		HP:0001417	OMIM:300085	TAS					I	HPO:probinson[2009-02-17]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0001265	PMID:15372378	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0003445	OMIM:182980	IEA					P	HPO:iea[2009-02-17]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0003596	PMID:15372378	PCS		7/8			C	HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0003693	PMID:15372378	PCS		1/8			P	HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0003394	PMID:15372378	PCS		7/8			P	HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0002460	PMID:15372378	PCS		1/8			P	HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0002380	PMID:15372378	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0007269	PMID:15372378	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0025710	PMID:15372378	PCS		1/8			C	HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0002505	PMID:15372378	PCS	HP:0003596	1/8			P	HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0007126	PMID:15372378	PCS		6/8			P	HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0003701	PMID:15372378	PCS		7/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0000006	PMID:15372378	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:182980	Spinal muscular atrophy, late-onset, Finkel type		HP:0001337	PMID:15372378	PCS		1/8			P	HPO:probinson[2022-08-08]
OMIM:616362	Houge-Janssens syndrome 2		HP:0010804	OMIM:616362	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616362	Houge-Janssens syndrome 2		HP:0002540	PMID:26168268	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0002188	PMID:26168268	PCS		2/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000463	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000122	PMID:26168268	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001250	PMID:26168268;PMID:25533962	PCS		6/8			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0002066	PMID:26168268	PCS		2/2			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001252	PMID:26168268;PMID:25533962	PCS		6/8			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001274	PMID:26168268	PCS		3/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0010721	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0010055	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0100704	PMID:26168268	PCS		2/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0012450	PMID:26168268	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000316	OMIM:616362	TAS				HP:0012825	P	HPO:skoehler[2015-11-15]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000238	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0002119	PMID:26168268	PCS		2/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001249	PMID:25533962	PCS		3/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000297	OMIM:616362	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000252	PMID:26168268	PCS		2/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000494	OMIM:616362	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001385	PMID:26168268	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001344	PMID:26168268	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0002650	PMID:26168268	PCS		2/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0002079	PMID:26168268;PMID:25533962	PCS		5/8			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0005487	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000194	OMIM:616362	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001382	PMID:26168268;PMID:25533962	PCS		2/8			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001263	PMID:26168268	PCS		5/5		HP:0012828	P	HPO:skoehler[2015-11-15];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0002194	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0100259	PMID:26168268	PCS		1/5			P	HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0009179	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000767	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000505	PMID:25533962	PCS	HP:0003577	1/3			P	HP:probinson[2018-09-01]
OMIM:616362	Houge-Janssens syndrome 2		HP:0001357	PMID:25533962	PCS		2/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000006	PMID:25533962	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616362	Houge-Janssens syndrome 2		HP:0000324	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:151500	Leukocyte nuclear appendages, hereditary prevalence of		HP:0001871	OMIM:151500	IEA					P	HPO:iea[2009-02-17]
OMIM:151500	Leukocyte nuclear appendages, hereditary prevalence of		HP:0000006	OMIM:151500	IEA					I	HPO:iea[2009-02-17]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0410175	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001290	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0100704	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001987	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0002119	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001324	PMID:18499082	PCS	HP:0003621	2/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001268	PMID:18499082	PCS	HP:0003621	2/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0002415	PMID:18499082	PCS		2/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0007965	PMID:18499082	PCS					P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001942	PMID:18499082;PMID:24781756	PCS		11/11			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0003688	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0003326	PMID:18499082	PCS	HP:0003621				P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0003348	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0003128	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0000572	PMID:18499082	PCS		2/2			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0002078	PMID:18499082	PCS					P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001640	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0011968	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0002151	PMID:18499082;PMID:24781756	PCS		3/3			P	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0002490	PMID:18499082	PCS					P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0002070	PMID:18499082	PCS					P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0002092	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0005180	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001639	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0000007	PMID:18499082	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001714	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619051	Mitochondrial complex IV deficiency, nuclear type 7		HP:0001511	PMID:24781756	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:126950	Dwarfism with tall vertebrae		HP:0003510	OMIM:126950	IEA					P	HPO:iea[2009-02-17]
OMIM:126950	Dwarfism with tall vertebrae		HP:0004570	OMIM:126950	IEA					P	HPO:iea[2009-02-17]
OMIM:126950	Dwarfism with tall vertebrae		HP:0002812	OMIM:126950	IEA					P	HPO:iea[2009-02-17]
OMIM:126950	Dwarfism with tall vertebrae		HP:0000006	OMIM:126950	IEA					I	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0003477	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0002321	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0003355	OMIM:609242	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609242	Kanzaki disease		HP:0002460	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0000280	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0001071	OMIM:609242	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:609242	Kanzaki disease		HP:0100543	OMIM:609242	TAS				HP:0012825	P	HPO:skoehler[2014-04-04]
OMIM:609242	Kanzaki disease		HP:0000958	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0040078	OMIM:609242	TAS					P	HPO:skoehler[2014-11-26]
OMIM:609242	Kanzaki disease		HP:0003409	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0002936	OMIM:609242	TAS					P	HPO:probinson[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0025710	PMID:8040340	PCS		1/1			C	HPO:probinson[2023-03-28]
OMIM:609242	Kanzaki disease		HP:0000179	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0001004	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0000214	OMIM:609242	TAS					P	HPO:probinson[2012-04-29]
OMIM:609242	Kanzaki disease		HP:0007428	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0002059	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0003581	OMIM:609242	IEA					C	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0003461	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0032325	PMID:8040340	PCS		1/1			P	HPO:probinson[2023-03-28]
OMIM:609242	Kanzaki disease		HP:0005280	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0000407	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:609242	Kanzaki disease		HP:0000503	PMID:8040340	PCS		1/1			P	HPO:probinson[2023-03-28]
OMIM:609242	Kanzaki disease		HP:0000007	PMID:8040340	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-28]
OMIM:609242	Kanzaki disease		HP:0000967	PMID:8040340	PCS		1/1			P	HPO:probinson[2023-03-28]
OMIM:609242	Kanzaki disease		HP:0000962	OMIM:609242	IEA					P	HPO:iea[2009-02-17]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0003676	PMID:24360804	PCS					C	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002067	OMIM:615643	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001332	PMID:24360804	PCS		2/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0003693	PMID:24360804	PCS		1/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002063	PMID:24360804	PCS		1/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002180	OMIM:615643	IEA					P	HPO:skoehler[2015-01-27]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0012048	PMID:24360804	PCS		1/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0033329	PMID:24360804	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0100034	PMID:24360804	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0000716	OMIM:615643	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0011463	PMID:24360804	PCS		2/2			C	HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0007002	PMID:24360804	PCS		2/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001268	OMIM:615643	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002313	OMIM:615643	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001249	PMID:24360804	PCS		2/2			P	HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001265	OMIM:615643	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002510	PMID:24360804	PCS		1/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001761	PMID:24360804	PCS		1/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002079	OMIM:615643	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001288	PMID:24360804	PCS		2/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002376	OMIM:615643	TAS					P	HPO:skoehler[2014-03-24]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0031936	PMID:24360804	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001260	PMID:24360804	PCS		2/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0001263	OMIM:615643	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0000722	PMID:24360804	PCS		1/2			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0000007	PMID:24360804	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0030051	PMID:24360804	PCS		2/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-25]
OMIM:615643	Neurodegeneration with brain iron accumulation 6		HP:0002522	PMID:24360804	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0002267	PMID:30031689	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001276	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0002188	PMID:30031689	PCS		2/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0004322	PMID:30031689	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001272	PMID:30031689	PCS		1/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001250	PMID:30031689	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0003097	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0006808	PMID:30031689	PCS		2/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0003593	PMID:30031689	PCS		1/2			C	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0005792	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001196	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0010845	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0010821	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0012498	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0100704	PMID:30031689	PCS		1/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0000737	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0003429	PMID:30031689	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001945	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0002015	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0006956	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0000252	PMID:30031689	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0000750	PMID:30031689	PCS		2/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0000574	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0002079	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0011968	PMID:30031689	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0000293	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0010819	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001263	PMID:30031689	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0011225	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001182	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0032792	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0000007	PMID:30031689	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0002307	PMID:30031689	PCS		1/2			P	HPO:probinson[2023-04-20]
OMIM:618367	Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination		HP:0001257	PMID:30031689	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:119550	Cleft palate-lateral synechia syndrome		HP:0000175	OMIM:119550	IEA					P	HPO:iea[2009-02-17]
OMIM:119550	Cleft palate-lateral synechia syndrome		HP:0000006	OMIM:119550	IEA					I	HPO:iea[2009-02-17]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0001276	PMID:27292112	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0003676	PMID:27292112	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0003236	PMID:27292112	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0002015	OMIM:617054	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0003376	PMID:27292112	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0000750	OMIM:617054	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0001332	PMID:27292112	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0002376	PMID:27292112	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0003781	PMID:27292112	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0001252	PMID:27292112	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0011448	PMID:27292112	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0012179	OMIM:617054	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0011463	PMID:27292112	PCS		2/2			C	HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0002938	PMID:27292112	PCS		1/2			P	HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0000007	PMID:27292112	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0002317	PMID:27292112	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0002505	PMID:27292112	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0002307	PMID:27292112	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617054	Striatonigral degeneration, childhood-onset		HP:0001347	OMIM:617054	TAS					P	HPO:skoehler[2017-07-13]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0002243	PMID:29408806	PCS		1/3			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0002013	PMID:29408806	PCS		1/3			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0002242	PMID:29408806	PCS					P	HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0005263	PMID:29408806	PCS					P	HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0032564	PMID:29408806	PCS					P	HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0033256	PMID:29408806	PCS					P	HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0025085	PMID:29408806	PCS		1/3			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0033117	PMID:29408806	PCS					P	HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0100633	PMID:29408806	PCS					P	HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0020002	PMID:29408806	PCS		1/3			P	HPO:probinson[2025-09-26];HPO:probinson[2025-09-26]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0000006	PMID:29408806	PCS					I	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0002027	PMID:29408806	IEA		3/3			P	HPO:probinson[2021-01-01]
OMIM:619079	Inflammatory bowel disease (Crohn disease) 30		HP:0002028	PMID:29408806	IEA		3/3			P	HPO:probinson[2021-01-01]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002300	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0003676	OMIM:606159	IEA					C	HPO:skoehler[2010-06-19]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0003596	PMID:11438811	PCS					C	HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002067	PMID:17142829	PCS		13/38			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001332	PMID:17142829	PCS		32/38			P	HPO:probinson[2021-07-16];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002063	PMID:11438811	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001251	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002180	OMIM:606159	IEA					P	HPO:skoehler[2015-01-27]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0012049	OMIM:606159	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0007123	OMIM:606159	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0031908	OMIM:606159	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0000338	PMID:17142829	PCS		13/38			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0000712	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0000734	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0007007	OMIM:606159	IEA					P	HPO:iea[2009-02-17]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001347	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002356	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002015	PMID:17142829	PCS		15/38			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001300	OMIM:606159	IEA					P	HPO:iea[2009-02-17]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001266	PMID:11438811	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0003487	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001260	PMID:17142829	PCS		25/38			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002072	PMID:17142829	IEA		27/38			P	HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0100660	OMIM:606159	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0012343	PMID:17142829	PCS		9/11	MALE		P	HPO:skoehler[2013-09-17];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0012343	PMID:17142829	PCS		3/13	FEMALE		P	HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001618	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0000726	OMIM:606159	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0002425	OMIM:606159	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001257	OMIM:606159	IEA					P	HPO:iea[2009-02-17]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0001337	PMID:17142829	PCS		2/38			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0000006	PMID:11438811	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-16]
OMIM:606159	Neurodegeneration with brain iron accumulation 3		HP:0000643	OMIM:606159	IEA					P	HPO:iea[2009-02-17]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0010529	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000486	PMID:33350388	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000463	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001250	PMID:33350388	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001252	PMID:33350388	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001251	PMID:33350388	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0410170	PMID:33350388	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0012104	PMID:33350388	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001629	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000319	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000316	PMID:33350388	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001822	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0006970	PMID:33350388	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000455	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001249	PMID:33350388	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000252	PMID:33350388	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000670	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000494	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001344	PMID:33350388	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001288	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0002079	PMID:33350388	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0011968	PMID:33350388	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001263	PMID:33350388	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001680	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0004691	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000627	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000729	PMID:33350388	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000767	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0004209	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0002007	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000520	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0001631	PMID:33350388	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000369	PMID:33350388	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000347	PMID:33350388	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:620820	El Hayek-Chahrour neurodevelopmental syndrome		HP:0000006	PMID:33350388	PCS					I	ORCID:0000-0002-0736-9199[2024-07-01]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0000220	PMID:29016863	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0002015	PMID:29016863	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0010628	PMID:29016863	PCS		11/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0003680	PMID:29016863	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0410263	PMID:29016863	PCS		0/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0003593	PMID:29016863	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0000508	PMID:29016863	PCS		11/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0000006	PMID:29016863	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0011469	PMID:29016863	PCS		5/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-19]
OMIM:617732	Facial palsy, congenital, with ptosis and velopharyngeal dysfunction		HP:0001611	PMID:29016863	PCS		11/11			P	HPO:probinson[2023-03-19]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003774	PMID:12913070	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001870	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0005995	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000464	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0009839	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000320	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001596	OMIM:608612	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003077	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001371	PMID:12913070	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000160	PMID:12913070	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003196	PMID:12913070	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003593	PMID:12913070	PCS		1/1			C	HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001070	PMID:12913070	PCS	HP:0003621	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003074	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0008070	PMID:12913070	PCS	HP:0003621	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0009064	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000418	PMID:12913070	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0009002	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000678	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000218	OMIM:608612	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000894	PMID:12913070	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0009803	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0005328	PMID:12913070	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000831	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0004334	PMID:12913070	PCS	HP:0011463	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0002299	PMID:12913070	PCS	HP:0003621	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000292	PMID:12913070	PCS	HP:0003621	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000270	PMID:12913070	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0006480	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000905	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0100613	PMID:12913070	PCS		1/1			C	HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000007	PMID:12913070	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0002645	OMIM:608612	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003635	PMID:12913070	PCS	HP:0003621	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000520	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001015	PMID:12913070	PCS	HP:0003621	1/1			P	HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000685	OMIM:608612	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001510	PMID:12913070	PCS		1/1			P	HPO:probinson[2022-06-20]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000347	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000842	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
OMIM:608612	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001952	OMIM:608612	IEA					P	HPO:iea[2009-02-17]
DECIPHER:59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0011096	DECIPHER:59	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0012332	DECIPHER:59	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0007256	DECIPHER:59	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0002415	DECIPHER:59	IEA					P	HPO:skoehler[2013-05-29]
OMIM:613554	Von willebrand disease, type 2		HP:0000132	OMIM:613554	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613554	Von willebrand disease, type 2		HP:0003828	OMIM:613554	TAS					M	HPO:skoehler[2012-10-17]
OMIM:613554	Von willebrand disease, type 2		HP:0000007	OMIM:613554	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613554	Von willebrand disease, type 2		HP:0000978	OMIM:613554	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613554	Von willebrand disease, type 2		HP:0000421	OMIM:613554	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613554	Von willebrand disease, type 2		HP:0001873	OMIM:613554	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613554	Von willebrand disease, type 2		HP:0000006	OMIM:613554	TAS					I	HPO:skoehler[2012-10-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0004325	OMIM:271640	TAS					P	HPO:skoehler[2013-08-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003510	PMID:23664117	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001371	OMIM:271640	TAS					P	HPO:skoehler[2013-08-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0430047	PMID:23664117	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001252	PMID:23664117	PCS		1/7			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0010049	PMID:23664117	PCS		5/5			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0011341	PMID:23664117	PCS		3/5			P	HPO:skoehler[2013-08-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0011220	PMID:23664117	PCS		4/5			P	HPO:skoehler[2013-08-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001647	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000878	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002857	OMIM:271640	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0009702	PMID:23664117	PCS		1/5			P	HPO:skoehler[2013-08-18];HPO:probinson[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002656	OMIM:271640	IEA					P	HPO:skoehler[2018-10-08]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001840	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001763	OMIM:271640	IEA		3/5			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002751	PMID:23664117	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003048	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000175	OMIM:271640;PMID:23664117	PCS		10/15			P	ORCID:0000-0002-0736-9199[2024-07-03];HPO:iea[2009-02-17];HPO:probinson[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002673	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001222	PMID:23664117	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001382	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0011800	OMIM:271640	TAS					P	HPO:skoehler[2015-11-15]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003083	OMIM:271640	TAS					P	HPO:skoehler[2013-04-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002827	OMIM:271640;PMID:23664117	PCS		11/17			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000926	PMID:23664117	PCS	HP:0011463	7/7			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002869	OMIM:271640	TAS					P	HPO:probinson[2013-08-11]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000007	OMIM:271640;PMID:23664117	PCS		20/20			I	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000887	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002986	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002822	PMID:23664117	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001653	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000520	PMID:23664117	PCS		3/5			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0004568	PMID:23664117	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003015	PMID:23664117	PCS		7/7			P	HPO:skoehler[2013-08-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003016	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0008828	OMIM:271640	TAS					P	HPO:iea[2015-03-08]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000343	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001030	OMIM:271640	TAS					P	HPO:skoehler[2013-08-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0012368	PMID:23664117	PCS		4/5			P	HPO:probinson[2015-02-28]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0100864	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000939	OMIM:271640	TAS					P	HPO:skoehler[2013-08-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0006094	PMID:23664117	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001629	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0010550	OMIM:271640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0030043	OMIM:271640	TAS					P	HPO:skoehler[2015-01-20]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001547	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001822	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000218	OMIM:271640	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001027	PMID:23664117	PCS		2/5			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002756	OMIM:271640	TAS					P	HPO:skoehler[2013-10-06]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000974	PMID:23664117	PCS		2/5		HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000973	PMID:23664117	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002996	PMID:23664117	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003301	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003026	OMIM:271640	TAS					P	HPO:probinson[2012-05-27]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001762	PMID:23664117	PCS		2/7			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003300	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002651	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0004233	OMIM:271640;PMID:23664117	PCS		13/15			P	HPO:skoehler[2013-08-18];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0008818	OMIM:271640	IEA		5/5			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0003100	OMIM:271640	TAS					P	HPO:skoehler[2013-04-09]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002176	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000592	PMID:23664117	PCS		3/5			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000272	OMIM:271640	TAS					P	HPO:skoehler[2015-04-05]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000470	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0010575	PMID:23664117	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001083	OMIM:271640	TAS					P	HPO:probinson[2013-08-11]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0009473	PMID:23664117	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000904	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0002209	OMIM:271640;PMID:23664117	PCS		10/15			P	HPO:skoehler[2013-08-18];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001631	OMIM:271640	IEA		5/5			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000300	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0009836	OMIM:271640	IEA					P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0008824	PMID:23664117	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000347	PMID:23664117	PCS		4/7			P	HPO:skoehler[2013-08-18];HPO:probinson[2024-07-03]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0000545	OMIM:271640;PMID:23664118	PCS		20/20		HP:0012825	P	HP:probinson[2018-07-08];HPO:iea[2009-02-17]
OMIM:271640	Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures		HP:0001799	OMIM:271640	TAS					P	HPO:iea[2009-02-17]
OMIM:602459	Deafness, autosomal dominant 15		HP:0000365	OMIM:602459	IEA		HP:0040280			P	HPO:skoehler[2013-01-11]
OMIM:602459	Deafness, autosomal dominant 15		HP:0000006	OMIM:602459	IEA					I	HPO:skoehler[2013-01-09]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0003577	PMID:21271648	PCS		28/28			C	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0003038	PMID:21271648	PCS		23/24			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0010109	PMID:21271648	PCS		28/28			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0004322	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0008807	OMIM:268305	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000160	PMID:21271648;PMID:24360810	PCS		52/53			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0005011	PMID:21271648	PCS		14/27			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0010049	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0010487	PMID:21271648	PCS		20/24			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0001608	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0009486	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0030043	OMIM:268305	TAS		HP:0040283			P	HPO:skoehler[2015-01-20]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0006355	PMID:21271648	PCS		20/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0009623	PMID:21271648	PCS		14/26			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0008753	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000218	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000411	OMIM:268305	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0005867	PMID:21271648	PCS		6/23			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0009803	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000175	PMID:24360810	PCS		19/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000750	PMID:21271648	PCS		15/19			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0001245	PMID:21271648	PCS		20/24			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0001762	PMID:21271648;PMID:24360810	PCS		52/53			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0011968	PMID:21271648	PCS		20/26			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000193	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0001263	PMID:21271648	PCS		11/25			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0010752	PMID:21271648	PCS		22/26			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0009094	OMIM:268305	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0100499	PMID:21271648	PCS		24/26			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000308	PMID:24360810	PCS		25/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0002827	OMIM:268305	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000448	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000007	PMID:24360810	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0004209	PMID:21271648	PCS		18/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0009237	PMID:21271648	PCS		23/27			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0008744	OMIM:268305	IEA					P	HPO:iea[2009-02-17]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000201	PMID:21271648	PCS		22/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0009778	PMID:21271648	PCS		26/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0005736	PMID:21271648	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0002984	PMID:21271648	PCS		24/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000369	OMIM:268305	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0004987	PMID:21271648	PCS		24/27			P	HPO:probinson[2022-09-06]
OMIM:268305	Robin sequence with cleft mandible and limb anomalies		HP:0000347	PMID:21271648	PCS		28/28			P	HPO:probinson[2022-09-06]
OMIM:601144	Brugada syndrome 1		HP:0001663	PMID:33221895	PCS		26/49			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0001695	PMID:33221895	PCS		11/49			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0005110	PMID:33221895	PCS		21/49			P	HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0011688	PMID:33221895	PCS		5/49			P	HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0011712	PMID:33221895	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0004749	PMID:33221895	PCS		3/49			P	HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0001279	PMID:33221895	PCS		27/49			P	HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0000006	PMID:33221895	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-07]
OMIM:601144	Brugada syndrome 1		HP:0001645	PMID:33221895	PCS					P	HPO:probinson[2021-02-07]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0005249	OMIM:243180	IEA					P	HPO:iea[2009-02-17]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0004389	PMID:33497358	PCS		1/3		HP:0011010	P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0000365	PMID:33497358	PCS		3/3			P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002013	OMIM:243180	IEA					P	HPO:skoehler[2010-06-20]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002574	OMIM:243180	TAS					P	HPO:probinson[2012-04-28]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0001260	OMIM:243180	IEA					P	HPO:iea[2009-02-17]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002066	OMIM:243180	IEA					P	HPO:iea[2009-02-17]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002253	OMIM:243180	IEA					P	HPO:iea[2009-02-17]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002495	OMIM:243180	TAS					P	HPO:probinson[2012-04-28]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0001284	OMIM:243180	IEA					P	HPO:iea[2009-02-17]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002251	PMID:33497358	PCS		5/5			P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0032466	PMID:33497358	PCS		3/4			P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0010831	OMIM:243180	TAS					P	HPO:probinson[2012-04-28]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0012332	PMID:33497358	PCS		1/3			P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0000508	PMID:33497358	PCS		2/3			P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0009830	PMID:33497358	PCS		1/3			P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0000007	PMID:33497358	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002804	PMID:33497358	PCS		3/6			P	HPO:probinson[2021-10-21]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0002566	OMIM:243180	IEA					P	HPO:iea[2009-02-17]
OMIM:243180	Visceral neuropathy, familial, autosomal recessive		HP:0000413	PMID:33497358	PCS		6/6			P	HPO:probinson[2021-10-21]
OMIM:618415	Cataract 48		HP:0003577	PMID:30290152	PCS		12/12			C	HPO:probinson[2023-03-15]
OMIM:618415	Cataract 48		HP:0000518	PMID:30290152	PCS	HP:0003577	12/12			P	HPO:probinson[2023-03-15]
OMIM:618415	Cataract 48		HP:0000616	PMID:30290152	PCS		2/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-15]
OMIM:618415	Cataract 48		HP:0012043	PMID:30290152	PCS		2/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-15]
OMIM:618415	Cataract 48		HP:0000646	PMID:30290152	PCS		4/12			P	HPO:probinson[2023-03-15]
OMIM:618415	Cataract 48		HP:0000007	PMID:30290152	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-15]
OMIM:618415	Cataract 48		HP:0007663	PMID:30290152	PCS		11/12			P	HPO:probinson[2023-03-15]
OMIM:618415	Cataract 48		HP:0000577	PMID:30290152	PCS		4/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-15]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0001034	PMID:25315659	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0009719	PMID:25315659	PCS		1/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0001596	PMID:25315659	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0002860	OMIM:618373	IEA		2/2		HP:0031796	P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0001480	PMID:25315659	PCS		1/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0003593	PMID:25315659	PCS		2/2			C	HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0002293	PMID:25315659	PCS		2/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0006480	PMID:25315659	PCS		1/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0000958	PMID:25315659	PCS		1/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0040189	PMID:25315659	PCS		1/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0000007	PMID:25315659	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0000524	PMID:25315659	PCS		1/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0008404	PMID:25315659	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0000982	OMIM:618373	IEA		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618373	Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma		HP:0005987	PMID:25315659	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:611431	Legius syndrome		HP:0000286	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0001012	PMID:17704776	PCS		11/40			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0001252	OMIM:611431	TAS					P	HPO:skoehler[2014-11-26]
OMIM:611431	Legius syndrome		HP:0002162	OMIM:611431	TAS					P	HPO:skoehler[2013-02-25]
OMIM:611431	Legius syndrome		HP:0000957	PMID:17704776;PMID:19366998	PCS		62/62			P	HPO:skoehler[2010-06-19];HP:probinson[2019-01-22];HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000316	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0001328	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0000997	PMID:19366998	PCS		10/18			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000218	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0000256	PMID:17704776;PMID:19366998	PCS		7/49			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000358	OMIM:611431	TAS					P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0001067	OMIM:611431	IEA		0/18			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000494	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0001480	PMID:17704776	PCS		14/43			P	HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000470	OMIM:611431	TAS					P	HPO:skoehler[2013-02-25]
OMIM:611431	Legius syndrome		HP:0034349	PMID:17704776	PCS		1/40		HP:0012825	P	HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000508	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0000767	PMID:17704776	PCS		3/40			P	HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0002705	OMIM:611431	TAS					P	HPO:skoehler[2015-12-30]
OMIM:611431	Legius syndrome		HP:0030052	PMID:19366998	PCS		9/18			P	HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0007018	PMID:17704776	PCS		2/40			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000006	PMID:17704776	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-17]
OMIM:611431	Legius syndrome		HP:0000347	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0000325	OMIM:611431	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611431	Legius syndrome		HP:0000369	OMIM:611431	TAS					P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:267750	Knobloch syndrome, type 1		HP:0000286	PMID:17546652;PMID:10942434	PCS		4/25			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001331	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001132	PMID:19160445;PMID:10942434;PMID:27259167;PMID:17975799	PCS		11/33			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000640	PMID:19160445	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002021	PMID:10942434	PCS		1/24			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001250	PMID:27259167	PCS		1/12			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0030211	PMID:17975799	PCS					P	HPO:probinson[2022-09-05]
OMIM:267750	Knobloch syndrome, type 1		HP:0001251	PMID:19160445	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0032794	PMID:19160445	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000081	PMID:10942434	PCS	HP:0003577	1/24			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0500087	PMID:20799329	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000639	PMID:17546652	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000639	PMID:20799329	PCS	HP:0003593	2/2			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000639	PMID:17975799	PCS		3/5			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0011463	PMID:19160445	PCS		1/1			C	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0011220	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000519	PMID:10942434	PCS		8/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001643	PMID:10942434	PCS	HP:0003577	1/24			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0007843	PMID:17975799	PCS		4/5			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001249	PMID:19160445	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000252	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001382	PMID:10942434;PMID:27259167	PCS		5/36			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001263	PMID:27259167	PCS		1/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0011800	PMID:10942434	PCS		3/14			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0011003	PMID:17546652;PMID:30007336;PMID:10942434;PMID:27259167;PMID:20799329	PCS		30/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12];HP:probinson[2022-03-12];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0100019	PMID:27259167	PCS		6/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000007	PMID:10942434	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000126	PMID:27259167	PCS		1/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000341	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0003577	PMID:17546652;PMID:17975799	PCS		6/6			C	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000585	PMID:17975799	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000541	PMID:17546652;PMID:10942434;PMID:27259167	PCS		18/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12];HP:probinson[2022-03-12];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0009917	PMID:27259167	PCS		3/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0030037	PMID:10942434	PCS	HP:0003577	1/24			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0030037	PMID:27259167	PCS		1/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001272	PMID:19160445	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0003298	PMID:10942434	PCS	HP:0003577	2/24			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0012805	PMID:27259167	PCS		5/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002085	PMID:10942434	PCS	HP:0003577	21/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002085	PMID:20799329	PCS		1/2			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002085	PMID:27259167	PCS		3/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000414	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002119	PMID:20799329	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002436	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0001104	PMID:30007336	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000533	PMID:30007336;PMID:27259167;PMID:17975799;PMID:20799329	PCS		21/21			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000275	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002059	PMID:19160445	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000075	PMID:27259167	PCS		1/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002293	PMID:27259167	PCS		1/12			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0005280	PMID:10942434	PCS		1/24			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0011228	PMID:17546652	PCS		1/1			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000506	PMID:10942434	PCS		1/24			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000667	PMID:17975799	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0007773	PMID:10942434;PMID:17975799	PCS		18/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000505	PMID:17546652;PMID:17975799;PMID:20799329	PCS		8/8			P	HP:probinson[2022-03-12];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000543	PMID:17975799	PCS		2/4			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000666	PMID:17546652	PCS		1/2			P	HP:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0000501	PMID:19160445	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:267750	Knobloch syndrome, type 1		HP:0002126	PMID:19160445;PMID:27259167	PCS		4/13			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0001561	PMID:14675180;PMID:15681471	PCS		5/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0000463	PMID:14675180	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0001057	PMID:14675180	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0004399	PMID:15681471	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0000430	PMID:14675180	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0001371	PMID:14675180	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0001030	PMID:14675180	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0000490	PMID:14675180	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0033802	PMID:15681471	PCS					P	HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0008066	PMID:14675180;PMID:15681471	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0011461	PMID:14675180	PCS		3/3			C	HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0008551	PMID:14675180	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0000007	PMID:14675180	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0003811	PMID:14675180	PCS		2/2			C	HPO:probinson[2022-03-26]
OMIM:612138	Epidermolysis bullosa simplex with pyloric atresia		HP:0000256	PMID:14675180	PCS		3/3			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:133540	Cockayne syndrome, type B		HP:0003510	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0007759	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000486	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001376	OMIM:133540	PCS					P	HPO:probinson[2012-03-17]
OMIM:133540	Cockayne syndrome, type B		HP:0002343	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0003278	OMIM:133540	TAS					P	HPO:probinson[2013-04-08]
OMIM:133540	Cockayne syndrome, type B		HP:0001250	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000083	OMIM:133540	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000680	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000482	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001251	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0003593	PMID:9443879	PCS		5/15			C	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000958	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000639	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0011463	PMID:9443879	PCS		6/15			C	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000519	PMID:9443879;PMID:18446857	PCS		8/14			P	HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0001525	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0008897	OMIM:133540	PCS					P	HPO:probinson[2012-03-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001324	OMIM:133540	TAS					P	HPO:probinson[2012-04-11]
OMIM:133540	Cockayne syndrome, type B		HP:0000633	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001249	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0005328	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0003469	OMIM:133540	PCS					P	HPO:probinson[2012-04-11]
OMIM:133540	Cockayne syndrome, type B		HP:0000252	PMID:18446857	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000054	PMID:18446857	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000970	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0004334	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0008839	OMIM:133540	TAS					P	HPO:probinson[2013-04-08]
OMIM:133540	Cockayne syndrome, type B		HP:0000292	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000490	PMID:18446857	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0010234	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000093	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000649	OMIM:133540	IEA					P	HPO:probinson[2012-03-18]
OMIM:133540	Cockayne syndrome, type B		HP:0000407	PMID:18446857	PCS		2/2			P	HPO:probinson[2012-03-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0007352	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000007	PMID:18446857	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000689	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000568	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000648	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0003758	PMID:18446857	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0007676	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000762	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000685	OMIM:133540	PCS					P	HPO:probinson[2012-03-17]
OMIM:133540	Cockayne syndrome, type B		HP:0002866	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001337	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000325	PMID:18446857	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0002545	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001595	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0003577	PMID:9443879;PMID:18446857	PCS		7/18			C	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000540	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0002684	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001271	PMID:18446857	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0003130	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0002240	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000580	OMIM:133540	IEA		11/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0011675	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0008070	OMIM:133540	TAS					P	HPO:skoehler[2013-08-07]
OMIM:133540	Cockayne syndrome, type B		HP:0011359	OMIM:133540	TAS					P	HPO:skoehler[2013-08-07]
OMIM:133540	Cockayne syndrome, type B		HP:0000939	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001508	PMID:18446857	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000417	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0007346	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000377	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001744	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0002135	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0003224	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0001000	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000670	PMID:9443879;PMID:18446857	PCS		7/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0002059	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000992	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0006958	OMIM:133540	IEA					P	HPO:probinson[2012-03-18]
OMIM:133540	Cockayne syndrome, type B		HP:0003819	PMID:18446857	PCS		3/3			C	HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0002808	PMID:18446857	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0001518	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0007495	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000987	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000822	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000426	PMID:18446857	PCS		3/3			P	HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0001511	PMID:18446857	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:133540	Cockayne syndrome, type B		HP:0000028	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:133540	Cockayne syndrome, type B		HP:0000303	OMIM:133540	IEA					P	HPO:iea[2009-02-17]
OMIM:304340	Pettigrew syndrome		HP:0001256	PMID:17186471;PMID:17617514	PCS		6/21			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0002684	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0001371	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0001250	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0002066	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0002187	PMID:17186471;PMID:17617514	PCS		4/21			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0001252	OMIM:304340;PMID:17617514	PCS		15/15			P	HPO:probinson[2023-06-08];HPO:skoehler[2014-11-26]
OMIM:304340	Pettigrew syndrome		HP:0003593	OMIM:304340	TAS					C	HPO:skoehler[2015-12-30]
OMIM:304340	Pettigrew syndrome		HP:0005450	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0000280	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0011463	PMID:17617514	PCS		1/5			C	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0000718	PMID:17186471;PMID:17617514	PCS		10/21			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0011220	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0012471	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0001305	OMIM:304340	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0000238	PMID:17617514	PCS		2/5			P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0007663	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0002119	PMID:17617514	PCS		1/5			P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0025116	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0012171	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0002514	OMIM:304340	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0001347	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0003623	PMID:17617514	PCS		4/5			C	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0002410	PMID:17617514	PCS		2/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0002135	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0001320	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0000154	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0000252	PMID:17186471	PCS		8/16			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0001344	PMID:17186471;PMID:17617514	PCS		10/21			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0000750	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0002650	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0001266	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0031936	PMID:17186471;PMID:17617514	PCS		16/21			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0000276	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0000490	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0005101	OMIM:304340	IEA					P	HPO:iea[2009-02-17]
OMIM:304340	Pettigrew syndrome		HP:0001263	PMID:17617514	PCS		5/5			P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0000407	OMIM:304340	IEA					P	HPO:iea[2009-02-17]
OMIM:304340	Pettigrew syndrome		HP:0001419	PMID:17186471	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0000448	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0000648	PMID:17617514	PCS		1/5			P	HPO:probinson[2023-06-08]
OMIM:304340	Pettigrew syndrome		HP:0100716	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0001257	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:304340	Pettigrew syndrome		HP:0000303	OMIM:304340	TAS					P	HPO:skoehler[2014-08-24]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000483	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000582	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000540	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000463	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0001250	PMID:32820033	PCS		5/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0003593	PMID:32820033	PCS		10/10			C	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0002282	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0001270	PMID:32820033	PCS		9/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0033725	PMID:32820033	PCS		6/9			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000518	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000639	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000637	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0200021	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000336	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000252	PMID:32820033	PCS		7/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000750	PMID:32820033	PCS		9/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0002057	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0001263	PMID:32820033	PCS		10/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000691	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0012385	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0006380	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000646	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000767	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000568	PMID:32820033	PCS		2/20			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0002967	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0001137	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000400	PMID:32820033	PCS		2/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0001257	PMID:32820033	PCS		3/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000006	PMID:32820033	PCS					I	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000501	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000347	PMID:32820033	PCS		2/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000445	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0000687	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619694	Developmental delay with variable neurologic and brain abnormalities		HP:0005338	PMID:32820033	PCS		1/10			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:137040	Gallbladder, agenesis of		HP:0001438	OMIM:137040	IEA					P	HPO:iea[2009-02-17]
OMIM:137040	Gallbladder, agenesis of		HP:0000006	OMIM:137040	IEA					I	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0003236	OMIM:608799	TAS					P	HPO:probinson[2012-03-18]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0003676	OMIM:608799	TAS					C	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000486	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001250	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001252	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0003593	OMIM:608799	TAS					C	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001251	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001290	OMIM:608799	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000639	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000319	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0003828	OMIM:608799	TAS					M	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000316	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001009	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001643	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0009824	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0005469	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0003642	OMIM:608799	TAS					P	HPO:probinson[2012-03-18]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000494	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0002353	OMIM:608799	TAS					P	HPO:probinson[2012-07-16]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0005543	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0002395	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0003560	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0012385	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0006380	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000007	OMIM:608799	IEA					I	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001976	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0002705	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000648	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0006466	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000488	OMIM:608799	TAS					P	HPO:skoehler[2015-07-26]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001337	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0002164	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0002240	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001508	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0100704	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0002910	OMIM:608799;PMID:10642602	PCS		20/20			P	HPO:probinson[2012-03-18];HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001103	PMID:16641202	TAS					P	HPO:probinson[2015-07-19]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001744	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0004855	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0001028	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0003645	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0006879	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0004279	OMIM:608799	TAS					P	HPO:probinson[2012-03-18]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0002098	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0005484	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0011344	OMIM:608799	TAS					P	HPO:probinson[2012-03-18]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0005280	OMIM:608799	IEA					P	HPO:iea[2009-02-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0200055	OMIM:608799	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608799	Congenital disorder of glycosylation, type IE		HP:0000347	OMIM:608799	TAS					P	HPO:skoehler[2014-04-13]
OMIM:620015	Advance sleep phase syndrome, familial, 4		HP:0031873	PMID:31138685	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:620015	Advance sleep phase syndrome, familial, 4		HP:0000006	PMID:31138685	PCS					I	HPO:probinson[2022-08-27]
OMIM:193090	Transcobalamin I deficiency		HP:0003401	OMIM:193090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:193090	Transcobalamin I deficiency		HP:0001939	OMIM:193090	IEA					P	HPO:iea[2009-02-17]
OMIM:193090	Transcobalamin I deficiency		HP:0000007	OMIM:193090	TAS					I	HPO:skoehler[2013-06-23]
OMIM:193090	Transcobalamin I deficiency		HP:0000006	OMIM:193090	IEA					I	HPO:iea[2009-02-17]
OMIM:193090	Transcobalamin I deficiency		HP:0001315	OMIM:193090	IEA					P	HPO:iea[2009-02-17]
OMIM:249240	Megalencephaly with dysmyelination		HP:0001355	OMIM:249240	PCS					P	HPO:probinson[2012-04-11]
OMIM:249240	Megalencephaly with dysmyelination		HP:0001250	OMIM:249240	PCS					P	HPO:probinson[2012-04-11]
OMIM:249240	Megalencephaly with dysmyelination		HP:0001251	OMIM:249240	PCS					P	HPO:probinson[2012-04-11]
OMIM:249240	Megalencephaly with dysmyelination		HP:0007266	OMIM:249240	PCS					P	HPO:probinson[2012-04-11]
OMIM:249240	Megalencephaly with dysmyelination		HP:0010852	OMIM:249240	PCS					P	HPO:probinson[2012-04-11]
OMIM:249240	Megalencephaly with dysmyelination		HP:0000007	OMIM:249240	PCS					I	HPO:probinson[2012-04-11]
OMIM:249240	Megalencephaly with dysmyelination		HP:0001257	OMIM:249240	PCS					P	HPO:probinson[2012-04-11]
OMIM:249240	Megalencephaly with dysmyelination		HP:0002500	OMIM:249240	PCS					P	HPO:probinson[2012-04-11]
OMIM:152800	Lymphangiectasia, intestinal		HP:0001595	OMIM:152800	IEA					P	HPO:iea[2009-02-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0002024	OMIM:152800	IEA					P	HPO:iea[2009-02-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0008360	OMIM:152800	IEA					P	HPO:iea[2009-02-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0000969	OMIM:152800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:152800	Lymphangiectasia, intestinal		HP:0002593	OMIM:152800	IEA					P	HPO:iea[2009-02-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0003826	OMIM:152800	IEA					C	HPO:skoehler[2010-06-20]
OMIM:152800	Lymphangiectasia, intestinal		HP:0001888	OMIM:152800	IEA					P	HPO:iea[2009-02-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0010741	OMIM:152800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0006641	OMIM:152800	IEA					P	HPO:iea[2009-02-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0000006	OMIM:152800	IEA					I	HPO:iea[2009-02-17]
OMIM:152800	Lymphangiectasia, intestinal		HP:0004315	OMIM:152800	IEA					P	HPO:iea[2009-02-17]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000341	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000286	PMID:33833410	PCS		2/6			P	HPO:probinson[2022-02-19];HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000582	PMID:33833410	PCS		4/6			P	HPO:probinson[2022-02-19];HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000483	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0003577	PMID:33833410	PCS		3/6			C	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001156	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001250	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0003593	PMID:33833410	PCS		3/6			C	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0012745	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0040082	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000718	PMID:33833410	PCS		3/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000219	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0002714	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000455	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000311	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000358	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000473	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000176	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000252	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000750	PMID:33833410	PCS		6/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0002870	PMID:33833410	PCS		2/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001263	PMID:33833410	PCS		6/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001182	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0032005	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0005280	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0100023	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0010677	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:4000079	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-04-15]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000729	PMID:33833410	PCS		6/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0011098	PMID:33833410	PCS		6/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000601	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000403	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001319	PMID:33833410	PCS	HP:0003577	3/3			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000565	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001357	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0007018	PMID:33833410	PCS		5/5			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0000006	PMID:33833410	PCS					I	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001337	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:619680	Marbach-Schaaf neurodevelopmental syndrome		HP:0001513	PMID:33833410	PCS		1/6			P	HPO:probinson[2022-02-19]
OMIM:617875	Polycystic liver disease 4 with or without kidney cysts		HP:0003829	OMIM:617875	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617875	Polycystic liver disease 4 with or without kidney cysts		HP:0000107	PMID:24706814	PCS	HP:0003581	14/25			P	HP:probinson[2018-07-04]
OMIM:617875	Polycystic liver disease 4 with or without kidney cysts		HP:0001407	PMID:24706814	PCS	HP:0003581	19/25			P	HP:probinson[2018-07-04]
OMIM:617875	Polycystic liver disease 4 with or without kidney cysts		HP:0000006	PMID:24706814	PCS					I	HP:probinson[2018-07-04]
OMIM:100820	Achoo syndrome		HP:0025096	PMID:2275931	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:100820	Achoo syndrome		HP:0000006	OMIM:100820	IEA					I	HPO:iea[2009-02-17]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0003577	PMID:29259162	PCS		3/3			C	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0000793	PMID:29259162	PCS		2/2			P	HPO:probinson[2022-06-01];HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001395	PMID:29259162	PCS		2/2			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0003040	PMID:29259162	PCS		1/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0002194	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001270	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0000093	PMID:29259162	PCS		3/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0100651	PMID:29259162	PCS		1/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0012156	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001508	PMID:29259162;PMID:31775019	PCS		2/4			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0032252	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:4000055	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0031693	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0000007	PMID:29259162	PCS					I	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0009125	PMID:29259162	PCS		1/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001954	PMID:29259162	PCS		3/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0009710	PMID:29259162	PCS		1/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001945	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001510	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001433	PMID:29259162	PCS	HP:0003623	3/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001433	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001876	PMID:29259162	PCS	HP:0003623	3/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0001876	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0002611	PMID:29259162	PCS		3/3			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0002028	PMID:31775019	PCS		1/1			P	HPO:probinson[2022-06-01]
OMIM:619858	Autoinflammatory-pancytopenia syndrome		HP:0003623	PMID:29259162	PCS		3/3			C	HPO:probinson[2022-07-20]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0006989	PMID:34385670	PCS		1/4			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0010804	PMID:34385670	PCS		3/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000343	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000463	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0002365	PMID:34385670	PCS		1/4			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0001371	PMID:34385670	PCS		2/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0001250	PMID:34385670	PCS		6/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0003593	PMID:34385670	PCS		3/6			C	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0008070	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0011182	PMID:34385670	PCS		5/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0001508	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000316	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000218	PMID:34385670	PCS		2/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000411	PMID:34385670	PCS		2/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000358	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0020206	PMID:34385670	PCS		2/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0001347	PMID:34385670	PCS		3/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0003623	PMID:34385670	PCS		3/6			C	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0008936	PMID:34385670	PCS		6/6			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0001320	PMID:34385670	PCS		3/4			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000494	PMID:34385670	PCS		2/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0002015	PMID:34385670	PCS		4/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000252	PMID:34385670	PCS		5/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0001344	PMID:34385670	PCS		3/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0005487	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0001263	PMID:34385670	PCS		6/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0100021	PMID:34385670	PCS		2/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0005280	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0032988	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0034353	PMID:34385670	PCS					P	HPO:probinson[2022-09-05]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000007	PMID:34385670	PCS					I	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000348	PMID:34385670	PCS		3/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000322	PMID:34385670	PCS		2/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000369	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0000303	PMID:34385670	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:620001	Neurodevelopmental disorder with spasticity, seizures, and brain abnormalities		HP:0009879	PMID:34385670	PCS		3/4			P	HPO:probinson[2022-08-28]
OMIM:168550	Parietal foramina with cleidocranial dysplasia		HP:0002697	OMIM:168550;PMID:14571277	PCS		20/20			P	HPO:probinson[2009-02-17];HPO:skoehler[2009-02-17]
OMIM:168550	Parietal foramina with cleidocranial dysplasia		HP:0025247	PMID:14571277	PCS					P	HPO:probinson[2017-06-17]
OMIM:168550	Parietal foramina with cleidocranial dysplasia		HP:0008551	PMID:14571277	PCS					P	HPO:probinson[2017-06-17]
OMIM:168550	Parietal foramina with cleidocranial dysplasia		HP:0004492	PMID:14571277	PCS					P	HPO:probinson[2009-02-17]
OMIM:168550	Parietal foramina with cleidocranial dysplasia		HP:0000894	PMID:14571277	PCS					P	HPO:probinson[2017-06-17]
OMIM:168550	Parietal foramina with cleidocranial dysplasia		HP:0000256	PMID:14571277	PCS					P	HPO:probinson[2017-06-17]
OMIM:168550	Parietal foramina with cleidocranial dysplasia		HP:0000006	PMID:14571277	PCS					I	HPO:probinson[2009-02-17]
OMIM:620767	Seckel syndrome 11		HP:0000582	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000340	PMID:38154379	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0003577	PMID:38154379	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000343	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0004322	PMID:38154379	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001270	PMID:38154379	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0010800	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000319	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000678	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000219	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0008897	PMID:38154379	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0030084	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0009765	PMID:38154379	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000218	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001302	PMID:38154379	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000411	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001643	PMID:38154379	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000278	PMID:38154379	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001249	PMID:38154379	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0004415	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0002553	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0002575	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000494	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000750	PMID:38154379	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001684	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0011968	PMID:38154379	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001263	PMID:38154379	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0100040	PMID:38154379	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0011451	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000426	PMID:38154379	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000007	PMID:38154379	PCS					I	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001159	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001511	PMID:38154379	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000347	PMID:38154379	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0009879	PMID:38154379	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0000687	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620767	Seckel syndrome 11		HP:0001655	PMID:38154379	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:604809	Panbronchiolitis, diffuse		HP:0003676	OMIM:604809	TAS					C	HPO:skoehler[2012-10-17]
OMIM:604809	Panbronchiolitis, diffuse		HP:0030831	OMIM:604809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604809	Panbronchiolitis, diffuse		HP:0030830	OMIM:604809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604809	Panbronchiolitis, diffuse		HP:0003651	OMIM:604809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604809	Panbronchiolitis, diffuse		HP:0002110	OMIM:604809	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604809	Panbronchiolitis, diffuse		HP:0012735	OMIM:604809	TAS					P	HPO:skoehler[2014-03-24]
OMIM:604809	Panbronchiolitis, diffuse		HP:0030828	OMIM:604809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604809	Panbronchiolitis, diffuse		HP:0012418	OMIM:604809	TAS					P	HPO:skoehler[2013-11-18]
OMIM:169100	Char syndrome		HP:0002553	OMIM:169100	PCS					P	HPO:probinson[2012-03-02]
OMIM:169100	Char syndrome		HP:0000486	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000574	OMIM:169100	PCS					P	HPO:probinson[2009-02-17]
OMIM:169100	Char syndrome		HP:0025234	OMIM:169100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:169100	Char syndrome		HP:0001263	OMIM:169100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:169100	Char syndrome		HP:0000508	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0009244	OMIM:169100	PCS					P	HPO:probinson[2009-02-17]
OMIM:169100	Char syndrome		HP:0000316	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000337	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000207	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0004209	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000411	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000455	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0001643	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000322	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000006	OMIM:169100	IEA					I	HPO:iea[2009-02-17]
OMIM:169100	Char syndrome		HP:0000369	OMIM:169100	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001410	PMID:12910490	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0002188	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000365	OMIM:124000	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003355	PMID:12910490	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001970	OMIM:124000	TAS					P	HPO:skoehler[2013-05-03]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003231	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001250	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003155	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001252	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001251	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001290	OMIM:124000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003074	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000518	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000716	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000712	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001405	PMID:12910490	PCS		2/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001324	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000510	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001249	OMIM:124000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0006558	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003546	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0002353	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003200	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003201	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0011924	PMID:12910490	PCS		2/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001263	PMID:12910490	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0002151	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0030948	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000007	PMID:12910490	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0030151	OMIM:124000	TAS					P	HPO:skoehler[2015-01-04]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001257	OMIM:124000	TAS					P	HPO:skoehler[2013-05-03]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001414	PMID:12910490	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0006789	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001397	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001396	PMID:12910490	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003577	PMID:12910490	PCS		2/2			C	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001272	PMID:12910490	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0032653	PMID:12910490	PCS		2/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001508	PMID:12910490	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000738	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001427	OMIM:124000	IEA					I	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001988	PMID:12910490	PCS		2/2			P	HPO:probinson[2022-11-09];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0008872	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001943	PMID:12910490	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003648	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0002910	PMID:12910490	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001942	PMID:12910490	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001347	OMIM:124000	TAS					P	HPO:skoehler[2013-05-03]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003128	PMID:12910490	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0008936	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0002059	OMIM:124000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0002299	OMIM:124000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0002171	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0001639	OMIM:124000	IEA					P	HPO:iea[2009-02-17]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0000508	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0003811	PMID:12910490	PCS		1/2			C	HPO:probinson[2022-11-09]
OMIM:124000	Mitochondrial complex III deficiency, nuclear type 1		HP:0004900	PMID:12910490	PCS		1/2			P	HPO:probinson[2022-11-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001531	PMID:20170897	PCS	HP:0003593	10/10			P	HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001377	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001971	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0004322	PMID:31091003;PMID:30705142	PCS		2/2			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001252	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002020	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001290	PMID:20170897	PCS		6/10			P	HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0004482	PMID:31091003;PMID:20170897	PCS		10/11			P	HPO:probinson[2020-10-06];HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0100651	PMID:20170897;PMID:30705142	PCS		2/11			P	HPO:probinson[2020-08-09];HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001409	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002938	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000316	PMID:31091003	IEA		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000954	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000872	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000358	PMID:20170897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000453	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002750	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000331	PMID:20170897;PMID:30705142	PCS		11/11			P	HPO:probinson[2020-10-06];HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001263	PMID:20170897;PMID:30705142	PCS		11/11			P	HPO:probinson[2020-10-06];HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0004570	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0011800	PMID:20170897	PCS					P	HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0012385	PMID:31091003;PMID:20170897	PCS		11/11			P	HPO:probinson[2020-10-06];HPO:skoehler[2013-10-22];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000767	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000007	PMID:20170897	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000444	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000520	PMID:20170897;PMID:30705142	PCS		11/11			P	HPO:probinson[2020-10-06];HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000322	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0005659	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000369	PMID:20170897	PCS	HP:0003593				P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000369	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002028	PMID:20170897;PMID:30705142	PCS		3/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-06];HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002960	PMID:20170897;PMID:30705142	PCS		7/11			P	HPO:skoehler[2015-01-27];HPO:probinson[2020-08-09];HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0006528	PMID:20170897	PCS		9/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002240	PMID:20170897	PCS		9/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001270	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0032342	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0008872	PMID:31091003	IEA		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001822	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0030084	PMID:20170897	PCS					P	HPO:skoehler[2014-09-21];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0009765	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001744	PMID:20170897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0003100	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0012115	PMID:20170897	PCS		3/10			P	HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0011471	PMID:20170897	PCS	HP:0003593	6/10			P	HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000508	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001999	PMID:20170897	PCS		10/10			P	HPO:skoehler[2015-01-19];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000821	PMID:20170897	PCS		4/10			P	HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000268	PMID:20170897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002007	PMID:20170897;PMID:30705142	PCS		11/11			P	HPO:probinson[2020-10-06];HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002205	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0002720	PMID:31091003	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0001876	PMID:30705142	PCS		1/1			P	HPO:probinson[2020-10-06]
OMIM:613385	Autoimmune disease, multisystem, with facial dysmorphism		HP:0000269	PMID:20170897	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0003774	PMID:18796626	PCS		8/14			P	HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0003621	PMID:18796626	PCS		2/14			C	HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0005575	PMID:18796626	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0005421	PMID:18796626	PCS		14/14			P	HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0000790	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0003581	PMID:18796626	PCS		7/14			C	HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0003593	PMID:18796626	PCS		2/14			C	HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0000093	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0001919	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0001937	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0001903	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0011463	PMID:18796626	PCS		3/14			C	HPO:probinson[2022-10-04];HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0000822	OMIM:612925	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0100519	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0001873	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0000006	PMID:18796626	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-04]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0003138	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612925	Hemolytic uremic syndrome, atypical, susceptibility to, 5		HP:0003259	OMIM:612925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615092	Left ventricular noncompaction 7		HP:0030682	PMID:23314057	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-10]
OMIM:615092	Left ventricular noncompaction 7		HP:0011664	PMID:23314057	PCS					P	HPO:probinson[2015-07-22];HPO:probinson[2022-07-10]
OMIM:615092	Left ventricular noncompaction 7		HP:0000006	PMID:23314057	PCS					I	HPO:skoehler[2013-03-08];HPO:probinson[2022-07-10]
OMIM:157950	Molar I reinclusion		HP:0000164	OMIM:157950	IEA					P	HPO:iea[2009-02-17]
OMIM:157950	Molar I reinclusion		HP:0004209	OMIM:157950	IEA					P	HPO:iea[2009-02-17]
OMIM:157950	Molar I reinclusion		HP:0000006	OMIM:157950	IEA					I	HPO:iea[2009-02-17]
OMIM:157950	Molar I reinclusion		HP:0000303	OMIM:157950	IEA					P	HPO:iea[2009-02-17]
OMIM:120500	Commissural lip pits		HP:0004467	OMIM:120500	IEA					P	HPO:iea[2009-02-17]
OMIM:120500	Commissural lip pits		HP:0000006	OMIM:120500	IEA					I	HPO:iea[2009-02-17]
OMIM:120500	Commissural lip pits		HP:0002710	OMIM:120500	IEA					P	HPO:iea[2009-02-17]
OMIM:308220	Immunodeficiency, X-linked, with deficiency of 115,000 dalton surfaceglycoprotein		HP:0005386	PMID:6499285	PCS					P	HPO:probinson[2017-09-17]
OMIM:308220	Immunodeficiency, X-linked, with deficiency of 115,000 dalton surfaceglycoprotein		HP:0002718	PMID:6499285	PCS					P	HPO:probinson[2017-09-17]
OMIM:308220	Immunodeficiency, X-linked, with deficiency of 115,000 dalton surfaceglycoprotein		HP:0001417	PMID:6499285	PCS					I	HPO:skoehler[2009-02-17]
OMIM:308220	Immunodeficiency, X-linked, with deficiency of 115,000 dalton surfaceglycoprotein		HP:0004429	PMID:6499285	PCS					P	HPO:probinson[2017-09-17]
OMIM:308220	Immunodeficiency, X-linked, with deficiency of 115,000 dalton surfaceglycoprotein		HP:0011840	PMID:6499285	PCS					P	HPO:probinson[2017-09-17]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002025	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0011939	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001371	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001250	PMID:34163037	PCS		12/25			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000160	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001252	PMID:34163037	PCS		15/22			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0003593	PMID:29736926	PCS		1/1			C	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002020	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0032794	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002061	PMID:34163037	PCS		1/22			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0012389	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0008897	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000311	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002019	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001763	PMID:34163037	PCS		2/14			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001601	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001249	PMID:34163037	PCS					P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0003623	PMID:30513141	PCS		1/1			C	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002870	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001263	PMID:34163037;PMID:29736926	PCS		11/11			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002194	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0008081	PMID:34163037	PCS		2/14			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0012385	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000609	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001657	PMID:34163037	PCS		2/19			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0007359	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000520	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000006	PMID:29736926	PCS					I	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000369	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0010307	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0012725	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001270	PMID:34163037	PCS		17/24			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002080	PMID:34163037	PCS		2/25			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0005709	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000219	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002714	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0008936	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002015	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000750	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0001762	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000233	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0003186	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002172	PMID:34163037	PCS		8/19			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002092	PMID:29736926	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0005280	PMID:29736926;PMID:30513141	PCS		2/2			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0010536	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0032792	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002209	PMID:29736926;PMID:30513141	PCS		2/2			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0002007	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000586	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0007018	PMID:34163037	PCS		3/25			P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620029	Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures		HP:0000347	PMID:30513141	PCS		1/1			P	HPO:probinson[2022-10-05]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0001288	PMID:33977262	PCS		2/3			P	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0011968	PMID:33977262	PCS		1/3			P	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0000737	PMID:33977262	PCS		3/3			P	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0003593	PMID:33977262	PCS		3/3			C	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0033454	PMID:33977262	PCS		2/3			P	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0007359	PMID:33977262	PCS		1/3			P	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0002415	PMID:33977262	PCS		2/3		HP:0033184	P	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0000006	PMID:33977262	PCS					I	HPO:probinson[2022-08-13]
OMIM:619864	Leukodystrophy, childhood-onset, remitting		HP:0002500	PMID:33977262	PCS		1/3		HP:0033184	P	HPO:probinson[2022-08-13]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0001706	PMID:14567970	PCS					P	HPO:probinson[2013-03-04]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0006670	PMID:12507422	PCS					P	HPO:probinson[2013-03-04]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0003581	PMID:12507422	PCS		10/10			C	HPO:probinson[2022-07-04]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0001635	PMID:12507422	PCS		8/10			P	HPO:probinson[2022-07-04]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0012664	PMID:12507422	PCS		5/5			P	HPO:probinson[2022-07-04]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0033755	PMID:12507422	PCS		6/6			P	HPO:probinson[2022-07-04]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0000006	PMID:12507422	PCS					I	HPO:probinson[2013-01-09]
OMIM:607482	Cardiomyopathy, dilated, 1M		HP:0001644	PMID:12507422	PCS		6/6			P	HPO:probinson[2013-03-04];HPO:probinson[2022-07-04]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0003676	OMIM:213600	IEA					C	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002067	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001332	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002461	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001250	PMID:22327515	PCS	HP:0011463	2/8			P	HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0004363	PMID:22327515	PCS		0/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002063	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0000020	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0000716	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0011463	PMID:22327515	PCS		2/8			C	HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0031908	OMIM:213600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001268	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001347	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002135	PMID:22327515	PCS		6/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001300	OMIM:213600	IEA		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001288	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0000298	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002354	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001260	OMIM:213600	IEA		1/8			P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0003581	PMID:22327515	PCS		8/8			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001263	PMID:22327515	PCS		2/8			P	HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002075	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002072	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002172	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0000709	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0007256	OMIM:213600	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002504	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002406	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0002305	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0000006	PMID:22327515	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:213600	Basal ganglia calcification, idiopathic, 1		HP:0001337	OMIM:213600	IEA					P	HPO:iea[2009-02-17]
OMIM:617691	Spinocerebellar ataxia 44		HP:0002015	PMID:28886343	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0000750	PMID:28886343	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0001310	PMID:28886343	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0001272	PMID:28886343	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0001260	PMID:28886343	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0002066	PMID:28886343	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0001251	PMID:28886343	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0002075	PMID:28886343	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0000360	PMID:28886343	PCS		3/7			P	HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0001270	PMID:28886343	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0002359	PMID:28886343	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0001257	PMID:28886343	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0000006	PMID:28886343	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0007338	PMID:28886343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0003677	PMID:28886343	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-31]
OMIM:617691	Spinocerebellar ataxia 44		HP:0001348	PMID:28886343	PCS		1/7			P	HPO:probinson[2021-05-31]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0000494	OMIM:209880	IEA					P	HPO:iea[2009-02-17]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0006747	PMID:12640453	PCS		1/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0003005	OMIM:209880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0003577	PMID:15121777	PCS		24/27			C	HPO:probinson[2021-07-06]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0031857	PMID:12640453	PCS		4/20			P	HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0011968	OMIM:209880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0002791	PMID:12640453	PCS		20/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0002251	PMID:14566559;PMID:12640453;PMID:15121777	PCS		17/57			P	HPO:probinson[2021-09-23];HPO:iea[2009-02-17];HPO:probinson[2021-07-06]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0003593	PMID:14566559	PCS		8/10			C	HPO:probinson[2021-09-23];HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0012416	OMIM:209880	IEA					P	HPO:skoehler[2018-10-08]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0004370	OMIM:209880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0031861	PMID:12640453	PCS		14/16			P	HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0012418	OMIM:209880	IEA					P	HPO:skoehler[2018-10-08]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0012332	PMID:15121777	PCS					P	HPO:probinson[2021-07-06]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0007110	PMID:15121777	PCS		27/27			P	HPO:skoehler[2015-01-27];HPO:probinson[2021-07-06]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0012450	PMID:14566559;PMID:12640453	PCS		5/30			P	HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0000975	OMIM:209880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0002877	PMID:14566559	PCS		10/10			P	HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0002104	OMIM:209880	IEA					P	HPO:skoehler[2018-10-08]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0000006	PMID:12640453	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0000369	OMIM:209880	IEA					P	HPO:iea[2009-02-17]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0003006	PMID:12640453	PCS		1/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-23]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0000358	OMIM:209880	IEA					P	HPO:iea[2009-02-17]
OMIM:209880	Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease		HP:0003623	PMID:14566559	PCS		2/10			C	HPO:probinson[2021-09-23]
OMIM:217300	Cornea plana 2		HP:0100689	OMIM:217300	TAS					P	HPO:skoehler[2014-06-24]
OMIM:217300	Cornea plana 2		HP:0007957	PMID:11726611	PCS		4/4			P	HPO:probinson[2022-10-08]
OMIM:217300	Cornea plana 2		HP:0000540	OMIM:217300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217300	Cornea plana 2		HP:0001084	OMIM:217300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217300	Cornea plana 2		HP:0011463	PMID:11726611	PCS		4/4			C	HPO:probinson[2022-10-08]
OMIM:217300	Cornea plana 2		HP:0000007	PMID:10802664	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-08]
OMIM:217300	Cornea plana 2		HP:0000568	PMID:11726611	PCS		4/4			P	HPO:probinson[2022-10-08]
OMIM:217300	Cornea plana 2		HP:0007663	PMID:11726611	PCS		4/4			P	HPO:probinson[2022-10-08]
OMIM:217300	Cornea plana 2		HP:0007720	PMID:11726611	PCS		4/4			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-10-08]
OMIM:217300	Cornea plana 2		HP:0000647	PMID:11726611	PCS		4/4			P	HPO:probinson[2022-10-08]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0003577	PMID:24705253	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0001355	PMID:24705253	PCS		12/12			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0001344	OMIM:615938	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0001162	PMID:24705253	PCS		11/12			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0001263	PMID:24705253	PCS		11/11		HP:0012828	P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0007074	PMID:24705253	PCS		1/12			P	HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0011220	PMID:24705253	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0000238	PMID:24705253	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0002119	PMID:24705253	PCS		10/12			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0001159	PMID:24705253	PCS		0/12			P	HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0000256	PMID:24705253	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-13]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0002126	PMID:24705253	PCS		12/12			P	HPO:skoehler[2014-08-24]
OMIM:615938	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 3		HP:0000006	PMID:24705253	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:613391	Deafness, autosomal recessive 84		HP:0000365	OMIM:613391	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613391	Deafness, autosomal recessive 84		HP:0001751	OMIM:613391	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613391	Deafness, autosomal recessive 84		HP:0003593	OMIM:613391	IEA					C	HPO:skoehler[2010-06-19]
OMIM:613391	Deafness, autosomal recessive 84		HP:0000007	OMIM:613391	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613391	Deafness, autosomal recessive 84		HP:0001270	OMIM:613391	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610698	Macular degeneration, age-related, 4		HP:0000608	PMID:24906858	PCS	HP:0003584				P	HP:probinson[2018-07-08];HPO:probinson[2022-10-03]
OMIM:610698	Macular degeneration, age-related, 4		HP:0003581	PMID:24906858	PCS					C	HPO:probinson[2022-10-03]
OMIM:610698	Macular degeneration, age-related, 4		HP:0010982	OMIM:610698	IEA					I	HPO:probinson[2013-12-15]
OMIM:610698	Macular degeneration, age-related, 4		HP:0000006	PMID:24906858	PCS					I	HPO:probinson[2022-10-03]
OMIM:610840	Mitral valve prolapse, myxomatous 3		HP:0001653	PMID:31118289	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:610840	Mitral valve prolapse, myxomatous 3		HP:0000006	PMID:31118289	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:610840	Mitral valve prolapse, myxomatous 3		HP:0001634	PMID:31118289	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:610840	Mitral valve prolapse, myxomatous 3		HP:0003831	PMID:31118289	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:222350	DIAMINOPENTANURIA		HP:0001250	OMIM:222350	IEA					P	HPO:iea[2009-02-17]
OMIM:222350	DIAMINOPENTANURIA		HP:0003297	OMIM:222350	IEA					P	HPO:iea[2009-02-17]
OMIM:222350	DIAMINOPENTANURIA		HP:0001251	OMIM:222350	IEA					P	HPO:iea[2009-02-17]
OMIM:222350	DIAMINOPENTANURIA		HP:0003131	OMIM:222350	IEA					P	HPO:iea[2009-02-17]
OMIM:222350	DIAMINOPENTANURIA		HP:0000007	OMIM:222350	IEA					I	HPO:iea[2009-02-17]
OMIM:222350	DIAMINOPENTANURIA		HP:0002180	OMIM:222350	IEA					P	HPO:iea[2009-02-17]
OMIM:222350	DIAMINOPENTANURIA		HP:0001257	OMIM:222350	IEA					P	HPO:iea[2009-02-17]
OMIM:609322	Rhabdoid tumor predisposition syndrome 1		HP:0030392	OMIM:609322	TAS					P	HPO:skoehler[2015-06-22]
OMIM:609322	Rhabdoid tumor predisposition syndrome 1		HP:0000006	OMIM:609322	IEA					I	HPO:skoehler[2010-06-19]
OMIM:609322	Rhabdoid tumor predisposition syndrome 1		HP:0002885	OMIM:609322	IEA					P	HPO:skoehler[2010-06-19]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000384	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0003577	PMID:25561519	PCS		6/6			C	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000486	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0004322	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0003593	OMIM:616202	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616202	Cerebellofaciodental syndrome		HP:0002280	PMID:25561519	PCS		5/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0034259	PMID:25561519	PCS		2/6			P	HPO:probinson[2022-06-04]
OMIM:616202	Cerebellofaciodental syndrome		HP:0045075	PMID:25561519	PCS		6/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0033725	PMID:25561519	PCS		4/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0012110	PMID:25561519	PCS		2/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001629	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000518	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000718	PMID:25561519	PCS		2/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000679	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000954	PMID:25561519	PCS		2/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0002119	PMID:25561519	PCS		4/6			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0002857	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000675	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0006511	PMID:25561519	PCS		2/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001763	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001601	PMID:25561519	PCS		1/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001249	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0006118	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000252	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0002213	PMID:25561519	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0002650	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000750	PMID:25561519	PCS		6/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0002750	PMID:25561519	PCS		4/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001321	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0003100	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001263	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000470	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001182	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0006461	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000689	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000007	PMID:25561519	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0004209	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0001634	PMID:25561519	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000369	PMID:25561519	PCS		6/6			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-08]
OMIM:616202	Cerebellofaciodental syndrome		HP:0000028	PMID:25561519	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0002650	PMID:33053334	PCS		3/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0001552	PMID:33053334	PCS		2/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0002673	PMID:33053334	PCS		1/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0001382	PMID:33053334	PCS		3/3			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0001591	PMID:33053334	PCS		1/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0001252	PMID:33053334	PCS		2/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0003593	PMID:33053334	PCS		1/5			C	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0001270	PMID:33053334	PCS					P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0008081	PMID:33053334	PCS		1/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0000939	PMID:33053334	PCS		3/3			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0011463	PMID:33053334	PCS		2/5			C	HPO:probinson[2021-01-08];HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0011461	PMID:33053334	PCS		2/5			C	HPO:probinson[2021-01-08];HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0000926	PMID:33053334	PCS		1/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0008873	PMID:33053334	PCS		4/4			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0000767	PMID:33053334	PCS		2/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0002979	PMID:33053334	PCS		5/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0000007	PMID:33053334	PCS					I	HPO:probinson[2021-01-08];HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0002757	PMID:33053334	PCS					P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0002812	PMID:33053334	PCS		1/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0006488	PMID:33053334	PCS		3/6			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0002645	PMID:33053334	PCS		1/2			P	HPO:probinson[2021-01-08]
OMIM:619131	Osteogenesis imperfecta 21		HP:0001763	PMID:33053334	PCS		1/6			P	HPO:probinson[2021-01-08]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000175	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000054	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0004960	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001263	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001680	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001171	OMIM:600460	TAS					P	HPO:probinson[2009-02-17]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001629	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0003819	OMIM:600460	TAS					C	HPO:skoehler[2012-10-17]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000316	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001636	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000007	OMIM:600460	TAS					I	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001217	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0008589	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000400	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001643	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001510	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000047	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0001249	OMIM:600460	TAS					P	HPO:probinson[2009-02-17]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000369	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000204	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000028	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:600460	Cleft palate, cardiac defect, genital anomalies, and ectrodactyly		HP:0000049	OMIM:600460	TAS					P	HPO:probinson[2012-07-21]
OMIM:614415	Chilblain lupus 2		HP:6000263	PMID:21204240	PCS		1/1			P	HPO:probinson[2024-02-09]
OMIM:614415	Chilblain lupus 2		HP:0000992	PMID:21204240	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-25]
OMIM:614415	Chilblain lupus 2		HP:0011463	PMID:21204240	PCS		1/2			C	HPO:probinson[2023-01-25]
OMIM:614415	Chilblain lupus 2		HP:0003593	PMID:21204240	PCS		1/2			C	HPO:probinson[2023-01-25]
OMIM:614415	Chilblain lupus 2		HP:0009710	PMID:21204240	PCS		2/2			P	HPO:probinson[2023-01-25]
OMIM:614415	Chilblain lupus 2		HP:0000006	PMID:21204240	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-25]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0007517	PMID:19610084	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001377	OMIM:123790	IEA					P	HPO:iea[2009-02-17]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000160	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:6000950	PMID:12181710	PCS					P	HPO:probinson[2024-08-04]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0010609	PMID:18247426	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001804	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000316	PMID:18247426;PMID:19610084	PCS		2/2			P	HPO:probinson[2023-02-11];HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001845	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000238	PMID:18247426	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000956	PMID:19610084	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0020049	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000358	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0005469	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0003246	PMID:19610084	PCS		1/1	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000494	PMID:18247426	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000453	OMIM:123790	IEA					P	HPO:iea[2009-02-17]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000695	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000452	PMID:19610084	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001263	PMID:18247426	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0004450	PMID:18247426;PMID:19610084	PCS		2/2			P	HPO:probinson[2023-02-11];HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0011800	PMID:18247426;PMID:19610084	PCS		2/2			P	HPO:probinson[2023-02-11];HPO:skoehler[2013-11-28];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0009891	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0002308	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000648	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000048	OMIM:123790	IEA					P	HPO:iea[2009-02-17]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000047	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000520	PMID:19610084	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000006	PMID:18247426	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0003577	PMID:19610084	PCS		1/1			C	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0004467	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001792	OMIM:123790	IEA					P	HPO:iea[2009-02-17]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000189	PMID:19610084	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000463	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001274	OMIM:123790	IEA					P	HPO:iea[2009-02-17]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0010541	PMID:18247426;PMID:19610084	PCS		2/2			P	HPO:probinson[2021-02-10];HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0034361	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0008872	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0002119	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000218	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000059	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000212	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0005989	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000413	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0002676	PMID:18247426;PMID:19610084	PCS		2/2			P	HPO:probinson[2023-02-11];HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001545	PMID:18247426	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0001363	PMID:18247426	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0002098	OMIM:123790	IEA					P	HPO:iea[2009-02-17]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000193	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000272	OMIM:123790	IEA					P	HPO:iea[2009-02-17]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0005280	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0100876	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000508	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000822	PMID:18247426	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:123790	Beare-Stevenson cutis gyrata syndrome		HP:0000426	PMID:19610084	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:174810	Familial expansile osteolysis		HP:0002653	PMID:12362049	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-25]
OMIM:174810	Familial expansile osteolysis		HP:0003676	OMIM:174810	TAS					C	HPO:skoehler[2017-07-13]
OMIM:174810	Familial expansile osteolysis		HP:0006480	OMIM:174810	TAS					P	HPO:probinson[2015-03-22]
OMIM:174810	Familial expansile osteolysis		HP:0003155	OMIM:174810	TAS					P	HPO:probinson[2015-03-22]
OMIM:174810	Familial expansile osteolysis		HP:0025124	PMID:12362049	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-25]
OMIM:174810	Familial expansile osteolysis		HP:0006487	PMID:12362049	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:174810	Familial expansile osteolysis		HP:0000405	PMID:12362049	PCS		16/20			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-25]
OMIM:174810	Familial expansile osteolysis		HP:0003080	OMIM:174810	TAS					P	HPO:probinson[2009-02-17]
OMIM:174810	Familial expansile osteolysis		HP:0002756	OMIM:174810	TAS					P	HPO:probinson[2009-02-17]
OMIM:174810	Familial expansile osteolysis		HP:0000006	PMID:10615125	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-25]
OMIM:174810	Familial expansile osteolysis		HP:0002797	PMID:12362049	PCS		12/20			P	HPO:probinson[2015-03-22];HPO:probinson[2023-02-25]
OMIM:174810	Familial expansile osteolysis		HP:0002753	OMIM:174810	TAS					P	HPO:probinson[2015-03-22]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000044	PMID:20463092	PCS		5/8			P	HPO:probinson[2013-04-06];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000054	PMID:20463092	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0002750	OMIM:612702	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0410030	OMIM:612702	IEA		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0012506	OMIM:612702	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000407	PMID:20463092	PCS		2/8			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000458	OMIM:612702	TAS		1/8			P	HPO:probinson[2013-04-06];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0004409	PMID:20463092	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000218	OMIM:612702	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000823	PMID:20463092	PCS		2/8			P	HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000006	PMID:18596921	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000028	PMID:20463092	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:612702	Hypogonadotropic hypogonadism 6 with or without anosmia		HP:0000786	PMID:20463092	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0000670	PMID:7706760	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-12]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0003577	PMID:7706760	PCS		3/3			C	HPO:probinson[2022-05-12]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0002232	PMID:7706760	PCS		3/3			P	HPO:probinson[2022-05-12]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0100490	OMIM:226650	IEA					P	HPO:iea[2009-02-17]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0001808	OMIM:226650	IEA					P	HPO:iea[2009-02-17]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0008066	PMID:7706760	PCS		3/3			P	HPO:probinson[2022-05-12]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0006297	PMID:7706760	PCS		3/3			P	HPO:probinson[2022-05-12]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0000668	OMIM:226650	IEA					P	HPO:iea[2009-02-17]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0006089	OMIM:226650	IEA					P	HPO:iea[2009-02-17]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0000007	PMID:7706760	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-12]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0007556	OMIM:226650	IEA					P	HPO:iea[2009-02-17]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0008404	PMID:7706760;OMIM:226650	PCS		13/13			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-12]
OMIM:226650	Epidermolysis bullosa, junctional, Non-Herlitz type		HP:0200097	OMIM:226650	TAS					P	HPO:skoehler[2013-06-12]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0011463	PMID:21842496	PCS		6/6			C	HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0007340	PMID:21842496	PCS	HP:0011463	6/6			P	HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0007354	PMID:21842496	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0002061	PMID:21842496	PCS	HP:0011463	6/6			P	HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0009005	PMID:21842496	PCS	HP:0003621	6/6			P	HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0000007	PMID:21842496	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0002505	PMID:21842496	PCS	HP:0011462	2/6			P	HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0003677	PMID:21842496	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:614373	Amyotrophic lateral sclerosis 16, juvenile		HP:0001347	PMID:21842496	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:310490	Cowchock syndrome		HP:0003236	PMID:23217327	PCS		2/2			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-02-21]
OMIM:310490	Cowchock syndrome		HP:0000365	OMIM:310490	IEA					P	HPO:iea[2009-02-17]
OMIM:310490	Cowchock syndrome		HP:0003390	OMIM:310490	TAS					P	HPO:skoehler[2015-12-30]
OMIM:310490	Cowchock syndrome		HP:0100543	OMIM:310490	TAS		HP:0040283			P	HPO:skoehler[2014-04-04]
OMIM:310490	Cowchock syndrome		HP:0009053	PMID:23217327	PCS					P	HPO:probinson[2023-02-21]
OMIM:310490	Cowchock syndrome		HP:0000407	PMID:23217327	PCS		3/7			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-02-21]
OMIM:310490	Cowchock syndrome		HP:0001419	PMID:23217327	PCS					I	HPO:probinson[2012-04-18];HPO:probinson[2023-02-21]
OMIM:310490	Cowchock syndrome		HP:0007002	OMIM:310490	IEA					P	HPO:iea[2012-03-12]
OMIM:310490	Cowchock syndrome		HP:0002936	OMIM:310490	TAS					P	HPO:skoehler[2015-12-30]
OMIM:310490	Cowchock syndrome		HP:0025435	PMID:23217327	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:310490	Cowchock syndrome		HP:0001324	OMIM:310490	TAS					P	HPO:probinson[2012-04-18]
OMIM:310490	Cowchock syndrome		HP:0000763	OMIM:310490	IEA					P	HPO:iea[2012-03-12]
OMIM:310490	Cowchock syndrome		HP:0002910	PMID:23217327	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:310490	Cowchock syndrome		HP:0001249	PMID:23217327	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:310490	Cowchock syndrome		HP:0008944	PMID:23217327	PCS					P	HPO:probinson[2023-02-21]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0004787	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0001399	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0004396	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0002240	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0100651	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0012378	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0000007	PMID:31213488	PCS					I	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0002018	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0000872	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0002910	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0000952	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0001259	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:618549	Hepatitis, fulminant viral, susceptibility to		HP:0000225	PMID:31213488	PCS		1/1			P	HPO:probinson[2020-07-15];HPO:probinson[2020-07-15]
OMIM:616564	Noonan syndrome 10		HP:0000286	PMID:30368668	PCS		5/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000341	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0007517	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0002202	PMID:30368668	PCS	HP:0011461	1/5			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0010726	PMID:25795793	PCS		2/2			P	HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0004322	OMIM:616564;PMID:30368668	PCS		15/17			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0004482	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0045075	PMID:25795793;PMID:30368668	PCS		6/20			P	HPO:probinson[2021-05-19];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001929	PMID:25795793	PCS		1/3			P	HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0001629	PMID:30368668	PCS		1/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000957	PMID:30368668	PCS		1/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000316	PMID:25795793;PMID:30368668	PCS		16/17			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000953	PMID:30368668	PCS		5/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000218	PMID:30368668	PCS		3/6			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001643	PMID:30368668	PCS		1/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001642	PMID:25795793;PMID:30368668	PCS		5/19			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000974	PMID:30368668	PCS		2/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0003645	PMID:25795793	PCS		2/2			P	HPO:probinson[2021-05-19];HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0002212	PMID:25795793;PMID:30368668	PCS		5/20			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000494	PMID:25795793;PMID:30368668	PCS		13/16			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0002650	PMID:30368668	PCS		2/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001263	PMID:25795793	PCS		2/13			P	HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0001680	PMID:25795793	PCS		1/13			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0000470	PMID:25795793	PCS		4/9			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0032152	PMID:25795793	PCS		1/13			P	HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0001639	PMID:30368668	PCS		5/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0010880	PMID:30368668	PCS	HP:0011461	1/3			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0009891	PMID:30368668	PCS		5/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001718	OMIM:616564	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616564	Noonan syndrome 10		HP:0000508	PMID:25795793;PMID:30368668	PCS		14/16			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000767	PMID:30368668	PCS		1/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001712	PMID:25795793	PCS		1/12			P	HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0002967	PMID:30368668	PCS		2/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000768	PMID:30368668	PCS		2/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001631	PMID:25795793;PMID:30368668	PCS		5/19			P	HPO:probinson[2021-05-19];HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001653	PMID:25795793	PCS		1/12			P	HPO:probinson[2021-05-19];HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0000465	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0000006	PMID:25795793	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0000028	PMID:25795793	PCS		1/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0000369	PMID:30368668	PCS		7/7			P	HPO:probinson[2021-05-22]
OMIM:616564	Noonan syndrome 10		HP:0001634	PMID:25795793	PCS		2/12			P	HPO:probinson[2021-05-19]
OMIM:616564	Noonan syndrome 10		HP:0000962	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-22]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0002245	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0003577	PMID:23665959;PMID:30157302	PCS		4/5			C	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001770	PMID:23665959	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0010627	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001651	PMID:23665959;PMID:30157302	PCS		3/5			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0004322	PMID:23665959;PMID:30157302	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001250	PMID:23665959;PMID:30157302	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0012727	PMID:30157302	PCS		2/4			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0003196	PMID:30157302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0011755	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0031565	PMID:30157302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0010882	PMID:23665959;PMID:30157302	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0031348	PMID:23665959;PMID:30157302	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0011579	PMID:23665959;PMID:30157302	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001508	PMID:23665959;PMID:30157302	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001607	PMID:30157302	PCS		1/4			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001629	PMID:23665959;PMID:30157302	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0011461	PMID:30157302	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0011560	PMID:23665959;PMID:30157302	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001746	PMID:23665959;PMID:30157302	PCS		1/4			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000954	PMID:30157302	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000337	PMID:30157302	PCS		1/3			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000678	PMID:30157302	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000218	PMID:30157302	PCS		2/3			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001643	PMID:30157302	PCS		2/2			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001642	PMID:23665959	PCS		2/2			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001601	PMID:30157302	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000358	PMID:30157302	PCS		1/3			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0006315	PMID:30157302	PCS		1/1			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0006956	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001660	PMID:30157302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000276	PMID:30157302	PCS		1/4			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0005301	PMID:23665959;PMID:30157302	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001263	PMID:23665959;PMID:30157302	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0011800	PMID:30157302	PCS		2/3			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0010773	PMID:23665959	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0010772	PMID:23665959;PMID:30157302	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0005280	PMID:30157302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0031853	PMID:30157302	PCS		1/4			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0011669	PMID:23665959	PCS		1/2			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001719	PMID:23665959;PMID:30157302	PCS		4/5			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000007	PMID:23665959	PCS					I	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0007598	PMID:30157302	PCS		1/4			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0001631	PMID:23665959;PMID:30157302	PCS		5/5			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000006	PMID:26247899	PCS					I	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0002566	PMID:23665959;PMID:30157302	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000369	PMID:30157302	PCS		1/3			P	HPO:probinson[2022-02-18]
OMIM:619657	Congenital heart defects, multiple types, 8, with or without heterotaxy		HP:0000347	PMID:30157302	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001254	OMIM:606777	TAS					P	HPO:probinson[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0002268	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001250	OMIM:606777	TAS		15/20			P	HPO:skoehler[2010-06-20];HPO:probinson[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001251	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0003593	OMIM:606777	IEA					C	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0003470	OMIM:606777	TAS					P	HPO:probinson[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0011972	OMIM:606777	TAS					P	HPO:iea[2012-07-18]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0011973	OMIM:606777	TAS					P	HPO:iea[2012-07-18]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001328	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001269	OMIM:606777	TAS					P	HPO:probinson[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001249	OMIM:606777	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001347	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0007704	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0000750	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001289	OMIM:606777	TAS					P	HPO:probinson[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0002353	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001266	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0003487	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001260	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001263	OMIM:606777	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0005484	OMIM:606777	TAS					P	HPO:probinson[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001939	OMIM:606777	IEA					P	HPO:iea[2009-02-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0000007	OMIM:606777	TAS		HP:0040283			I	HPO:skoehler[2012-11-18]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001257	OMIM:606777	IEA					P	HPO:skoehler[2010-06-18]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0000006	PMID:9462754	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:606777	GLUT1 deficiency syndrome 1, infantile onset, severe		HP:0001336	OMIM:606777	TAS					P	HPO:probinson[2009-02-17]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000175	OMIM:616570	TAS		HP:0040283			P	HPO:skoehler[2015-10-16]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000252	PMID:24700531	PCS		5/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000992	OMIM:616570	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0001762	PMID:24700531	PCS		2/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0001321	PMID:24700531	PCS		1/5			P	HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0001263	OMIM:616570	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0001274	PMID:24700531	PCS		1/5			P	HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0007291	PMID:24700531	PCS		1/5			P	HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000969	OMIM:616570	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0001838	PMID:24700531	PCS		3/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0034198	PMID:24700531	PCS		5/5			C	HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0002804	PMID:24700531	PCS		5/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000007	PMID:24700531	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0001558	PMID:24700531	PCS		5/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000568	OMIM:616570	TAS		HP:0040283			P	HPO:skoehler[2015-10-16]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0002119	PMID:24700531	PCS		2/5			P	HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0001511	OMIM:616570	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000369	PMID:24700531	PCS		3/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2022-11-27]
OMIM:616570	Cerebrooculofacioskeletal syndrome 3		HP:0000347	PMID:24700531	PCS		3/5			P	HPO:skoehler[2015-10-16];HPO:probinson[2022-11-27]
OMIM:619643	Oocyte maturation defect 11		HP:0008222	PMID:34704130	PCS		2/2			P	HPO:probinson[2022-02-12]
OMIM:619643	Oocyte maturation defect 11		HP:0011462	PMID:34704130	PCS		2/2			C	HPO:probinson[2022-03-05]
OMIM:619643	Oocyte maturation defect 11		HP:0000007	PMID:34704130	PCS					I	HPO:probinson[2022-02-12]
OMIM:608996	Premature ovarian failure 3		HP:0008209	PMID:19429596	PCS					P	HPO:probinson[2013-01-09]
OMIM:608996	Premature ovarian failure 3		HP:0000013	OMIM:608996	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608996	Premature ovarian failure 3		HP:0000869	OMIM:608996	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608996	Premature ovarian failure 3		HP:0000006	PMID:19429596	PCS					I	HPO:probinson[2013-03-30]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0003577	OMIM:606763	TAS					C	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0001696	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0000365	OMIM:606763	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0001651	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0002098	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0002110	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0100582	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0012259	PMID:22387996	PCS					P	HPO:probinson[2013-04-07]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0012265	OMIM:606763	IEA					P	HPO:skoehler[2015-01-19]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0012263	OMIM:606763	TAS					P	HPO:probinson[2013-04-07]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0000789	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0000007	OMIM:606763	TAS					I	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0000246	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0002205	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606763	Ciliary dyskinesia, primary, 2		HP:0000388	OMIM:606763	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001332	PMID:11443547	PCS		1/2			P	HPO:skoehler[2010-06-20]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001250	OMIM:612716	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0003593	OMIM:612716	IEA					C	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001251	PMID:11443547	PCS		1/2			P	HPO:skoehler[2013-06-05]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0008297	OMIM:612716	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0000716	PMID:11443547	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0000718	PMID:11443547	PCS		1/2			P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0040210	PMID:11443547	PCS		0/2			P	HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0000657	OMIM:612716	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0000752	OMIM:612716	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0002359	PMID:11443547	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001249	OMIM:612716	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0008936	OMIM:612716	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0000252	PMID:11443547	PCS		1/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001266	OMIM:612716	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001260	OMIM:612716	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001263	PMID:11443547	PCS		2/2			P	HPO:probinson[2012-09-16];HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:6000563	PMID:22522443	PCS		9/9			P	HPO:probinson[2024-04-03]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0010553	PMID:11443547	PCS		1/2			P	HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0000007	OMIM:612716	TAS					I	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0004923	PMID:11443547	PCS		0/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0040206	PMID:11443547	PCS		0/2			P	HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001257	PMID:11443547	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001510	PMID:11443547	PCS		1/2			P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0001337	PMID:11443547	PCS		1/2			P	HPO:skoehler[2010-06-19]
OMIM:612716	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency		HP:0000006	PMID:15241655	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2020-07-17]
OMIM:191650	URETEROCELE		HP:0000070	OMIM:191650	IEA					P	HPO:iea[2009-02-17]
OMIM:191650	URETEROCELE		HP:0000081	OMIM:191650	IEA					P	HPO:iea[2009-02-17]
OMIM:191650	URETEROCELE		HP:0000006	OMIM:191650	IEA					I	HPO:iea[2009-02-17]
OMIM:162900	Epidermal nevus, somatic		HP:0001442	PMID:20805368;PMID:22087699	PCS		20/20			I	HPO:probinson[2020-07-20]
OMIM:162900	Epidermal nevus, somatic		HP:0001054	OMIM:162900	IEA					P	HPO:skoehler[2009-02-17]
OMIM:162900	Epidermal nevus, somatic		HP:0000995	OMIM:162900	IEA					P	HPO:skoehler[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0000286	PMID:23602711	PCS		3/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0003510	PMID:27587992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:230740	GAPO syndrome		HP:0000563	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0000486	PMID:27587992	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0000485	PMID:23602711	PCS		3/3			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0004322	PMID:23602711	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:230740	GAPO syndrome		HP:0005576	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0001250	OMIM:230740	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0003196	PMID:23602711	PCS		4/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0030939	PMID:27587992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:230740	GAPO syndrome		HP:0045075	PMID:23602711	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000639	PMID:23602711	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0012471	PMID:27587992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:230740	GAPO syndrome		HP:0000316	PMID:23602711	PCS		4/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001249	OMIM:230740	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0002353	OMIM:230740	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0002750	PMID:23602711	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001382	PMID:23602711	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001582	OMIM:230740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0010554	PMID:23602711	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:230740	GAPO syndrome		HP:0000649	PMID:23602711	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:230740	GAPO syndrome		HP:0001658	PMID:23602711	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:230740	GAPO syndrome		HP:0001537	PMID:23602711	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000007	PMID:23602711	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0002705	OMIM:230740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0000648	PMID:23602711	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000565	PMID:23602711	PCS		2/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0003774	PMID:23602711	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:230740	GAPO syndrome		HP:0010628	PMID:23602711	PCS		1/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001476	PMID:23602711	PCS		4/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000343	PMID:23602711	PCS		4/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001596	PMID:23602711;PMID:27587992	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000463	PMID:23602711	PCS		4/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001591	OMIM:230740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0002164	OMIM:230740	IEA					P	HPO:skoehler[2019-04-18]
OMIM:230740	GAPO syndrome		HP:0000260	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0002240	OMIM:230740	IEA					P	HPO:skoehler[2019-04-18]
OMIM:230740	GAPO syndrome		HP:0001270	OMIM:230740	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0012841	PMID:23602711	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:230740	GAPO syndrome		HP:0008070	PMID:27587992	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0200040	OMIM:230740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0011120	PMID:27587992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:230740	GAPO syndrome		HP:0000613	OMIM:230740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0000337	PMID:23602711	PCS		4/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0002119	OMIM:230740	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0002557	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0000411	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0000653	PMID:23602711	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000179	PMID:23602711	PCS		4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000336	PMID:27587992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:230740	GAPO syndrome		HP:0000594	PMID:23602711	PCS		2/3			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000274	PMID:27587992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:230740	GAPO syndrome		HP:0002650	OMIM:230740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230740	GAPO syndrome		HP:0003187	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0001043	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0005280	PMID:23602711	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0000706	PMID:23602711;PMID:27587992	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-06-29];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0002209	PMID:23602711	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:230740	GAPO syndrome		HP:0002007	PMID:23602711;PMID:27587992	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-06-29];HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001357	PMID:23602711	PCS		3/4			P	HPO:probinson[2023-01-28]
OMIM:230740	GAPO syndrome		HP:0001510	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0000586	PMID:27587992	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-29]
OMIM:230740	GAPO syndrome		HP:0000501	OMIM:230740	IEA					P	HPO:iea[2009-02-17]
OMIM:230740	GAPO syndrome		HP:0000347	PMID:23602711	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:616216	Thrombocytopenia 5		HP:0001903	PMID:25581430	PCS		1/13			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0000978	PMID:25581430	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0000967	PMID:25581430	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0005518	PMID:25807284	PCS		10/10			P	HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0000421	PMID:25581430	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0001873	PMID:25581430;PMID:25807284	PCS		23/23			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21];HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0004812	PMID:25807284	PCS		3/10			P	HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0000006	PMID:25581430	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-21]
OMIM:616216	Thrombocytopenia 5		HP:0001875	PMID:25581430	PCS		2/13			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-21]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0008936	PMID:32006098	PCS		4/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0032989	PMID:32006098	PCS		5/6			P	HPO:probinson[2021-01-07];HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0003577	PMID:32006098	PCS		1/5			C	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0000252	PMID:32006098	PCS		5/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0002510	PMID:32006098	PCS		1/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0002059	PMID:32006098	PCS		1/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0000750	PMID:32006098	PCS		6/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0002650	PMID:32006098	PCS		2/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0002079	PMID:32006098	PCS		1/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0001250	PMID:32006098	PCS		2/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0001272	PMID:32006098	PCS		1/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0002451	PMID:32006098	PCS		5/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0001263	PMID:32006098	PCS		6/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0003593	PMID:32006098	PCS		4/5			C	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0001290	PMID:32006098	PCS		6/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0100660	PMID:32006098	PCS		5/5			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0000737	PMID:32006098	PCS		6/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0100704	PMID:32006098	PCS		1/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0000007	PMID:32006098	PCS					I	HPO:probinson[2021-01-07];HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0008872	PMID:32006098	PCS		6/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0003429	PMID:32006098	PCS		1/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0001511	PMID:32006098	PCS	HP:0011461	1/6			P	HPO:probinson[2021-01-07]
OMIM:619125	Kaya-Barakat-Masson syndrome		HP:0001257	PMID:32006098	PCS		6/6			P	HPO:probinson[2021-01-07]
OMIM:617108	Sessile serrated polyposis cancer syndrome		HP:0032222	PMID:27081527	PCS					P	HP:probinson[2019-03-09]
OMIM:617108	Sessile serrated polyposis cancer syndrome		HP:0000006	OMIM:617108	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614429	Ventricular septal defect 1		HP:0003577	PMID:18672102	PCS					C	HPO:probinson[2022-11-08]
OMIM:614429	Ventricular septal defect 1		HP:0001629	PMID:18672102	PCS		9/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:614429	Ventricular septal defect 1		HP:0001636	PMID:18672102	PCS		1/12			P	HPO:probinson[2022-11-08]
OMIM:614429	Ventricular septal defect 1		HP:0006695	PMID:18672102	PCS		1/12			P	HPO:probinson[2022-11-08]
OMIM:614429	Ventricular septal defect 1		HP:0001631	OMIM:614429	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614429	Ventricular septal defect 1		HP:0001642	OMIM:614429	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614429	Ventricular septal defect 1		HP:0000006	PMID:18672102	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:190200	Tremor of intention, ataxia, and lipofuscinosis		HP:0001939	OMIM:190200	IEA					P	HPO:iea[2009-02-17]
OMIM:190200	Tremor of intention, ataxia, and lipofuscinosis		HP:0001251	OMIM:190200	IEA					P	HPO:iea[2009-02-17]
OMIM:190200	Tremor of intention, ataxia, and lipofuscinosis		HP:0002216	OMIM:190200	IEA					P	HPO:iea[2009-02-17]
OMIM:190200	Tremor of intention, ataxia, and lipofuscinosis		HP:0002080	OMIM:190200	IEA					P	HPO:iea[2009-02-17]
OMIM:190200	Tremor of intention, ataxia, and lipofuscinosis		HP:0000006	OMIM:190200	IEA					I	HPO:iea[2009-02-17]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001298	PMID:29483653	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0002521	PMID:29483653	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001894	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0002188	PMID:29483653	PCS					P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0003212	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0002384	PMID:29483653	PCS		2/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001290	PMID:29483653	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0032794	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0410151	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0025085	PMID:29483653	PCS	HP:0003593	3/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001508	PMID:29483653	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0033351	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0009789	PMID:29483653	PCS	HP:0003593	1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0002059	PMID:29483653	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0002079	PMID:29483653	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001263	PMID:29483653	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0033256	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0031379	PMID:29483653	PCS					P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0032170	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0000007	PMID:29483653	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0005419	PMID:29483653	PCS					P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0002205	PMID:29483653	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001257	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0005218	PMID:29483653	IEA		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001931	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0003237	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:618213	Inflammatory bowel disease, immunodeficiency, and encephalopathy		HP:0001974	PMID:29483653	PCS		1/3			P	HPO:probinson[2020-12-07]
OMIM:617120	Joubert syndrome 27		HP:0008936	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0010946	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0002066	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0001263	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0001252	PMID:24886560	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0001251	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0003593	PMID:24886560	PCS		2/2			C	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0010442	PMID:24886560	PCS		0/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0000657	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0000007	PMID:24886560	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0020045	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0002419	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0002007	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0000488	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0000179	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0001249	PMID:24886560	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-05]
OMIM:617120	Joubert syndrome 27		HP:0000325	PMID:24886560	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:300867	Kabuki syndrome 2		HP:0004325	PMID:33674768	PCS					P	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0000286	PMID:23913813	PCS	HP:0003577	2/5			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000486	PMID:33674768	TAS		15/48			P	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0001212	PMID:23913813	PCS		2/2			P	HPO:skoehler[2012-10-17];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000365	PMID:23076834	PCS		1/3			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0004322	PMID:23913813	PCS		5/5			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001250	PMID:23913813	PCS		1/3			P	HPO:skoehler[2015-05-31];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001252	OMIM:300867	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300867	Kabuki syndrome 2		HP:0000085	PMID:33674768	PCS		4/53			P	HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0001290	PMID:23913813	PCS		1/3			P	HPO:skoehler[2017-07-13];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0032315	PMID:22197486	PCS	HP:0003623	3/3			P	HP:probinson[2019-04-19]
OMIM:300867	Kabuki syndrome 2		HP:0000639	PMID:33674768	PCS		5/48			P	HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0000437	PMID:23913813	PCS		3/4			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000637	PMID:23913813	PCS		5/5			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0008897	PMID:23913813	PCS		4/4			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001642	OMIM:300867	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:300867	Kabuki syndrome 2		HP:0001007	PMID:23913813	PCS		1/3			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001249	PMID:23913813	PCS		5/5			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0002553	PMID:23913813	PCS		1/3			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000175	PMID:23913813	PCS		1/3			P	HPO:skoehler[2015-05-31];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000252	PMID:23913813	PCS		2/4			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000695	PMID:33674768	PCS		7/45			P	HPO:skoehler[2015-05-31];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0001382	PMID:23913813	PCS		2/4			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001263	PMID:23913813	PCS		4/4			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0002827	PMID:23913813	PCS		2/3			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000689	PMID:33674768	PCS		7/45			P	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0000403	PMID:23913813	PCS		2/5			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000527	OMIM:300867	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300867	Kabuki syndrome 2		HP:0000400	PMID:27302555	PCS		10/11			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000369	PMID:23354975	PCS		1/4			P	HPO:probinson[2019-01-24]
OMIM:300867	Kabuki syndrome 2		HP:0005338	OMIM:300867	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300867	Kabuki syndrome 2		HP:0001156	PMID:33674768	PCS		19/60			P	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0002000	PMID:23913813	PCS		2/3			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0008872	PMID:33674768	PCS		42/50			P	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0006695	OMIM:300867	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:300867	Kabuki syndrome 2		HP:0000218	PMID:23913813	PCS		3/4			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001423	PMID:33674768	PCS					I	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0000411	PMID:23913813	PCS		2/4			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000455	OMIM:300867	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300867	Kabuki syndrome 2		HP:0000378	OMIM:300867	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:300867	Kabuki syndrome 2		HP:0000592	PMID:27302555	PCS		6/11			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000196	PMID:23913813	PCS		1/4			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001680	PMID:33674768	TAS		8/60			P	HPO:skoehler[2012-10-16];HPO:probinson[2021-09-13]
OMIM:300867	Kabuki syndrome 2		HP:0000708	OMIM:300867	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300867	Kabuki syndrome 2		HP:0000668	PMID:23913813	PCS		2/4			P	HPO:skoehler[2013-03-08];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001998	PMID:27302555	PCS	HP:0003623	5/10			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0009237	PMID:23913813	PCS		1/4			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0007655	PMID:23913813	PCS		4/5			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001511	PMID:23913813	PCS	HP:0030674	2/4			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0001631	OMIM:300867	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:300867	Kabuki syndrome 2		HP:0000347	PMID:27302555	PCS		5/11			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000347	PMID:23913813	PCS		1/4			P	HP:probinson[2019-01-20]
OMIM:300867	Kabuki syndrome 2		HP:0000347	PMID:23076834	PCS	HP:0003593	1/3			P	HP:probinson[2019-01-20]
OMIM:610883	Potocki-Lupski syndrome		HP:0010529	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0002463	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000365	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0004322	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000243	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0001250	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0002020	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0001290	PMID:17357070	PCS	HP:0003593				P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0002381	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000319	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0000717	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000316	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000678	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0000752	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0003745	OMIM:610883	TAS					I	HPO:iea[2018-03-13]
OMIM:610883	Potocki-Lupski syndrome		HP:0000494	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000252	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0002474	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0002353	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0002079	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0001263	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000689	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0000325	PMID:17357070	PCS	HP:0003593				P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0001655	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0000540	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0005274	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0010863	PMID:17357070	PCS					P	HPO:iea[2012-03-01]
OMIM:610883	Potocki-Lupski syndrome		HP:0012448	OMIM:610883	TAS					P	HPO:skoehler[2013-11-28]
OMIM:610883	Potocki-Lupski syndrome		HP:0012210	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0001508	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000817	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0008872	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000733	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000337	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0001626	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000218	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0000154	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0002650	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0003146	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0002011	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0010535	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0001518	PMID:17357070	PCS					P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0200136	OMIM:610883	TAS					P	HPO:skoehler[2013-06-12]
OMIM:610883	Potocki-Lupski syndrome		HP:0000821	OMIM:610883	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610883	Potocki-Lupski syndrome		HP:0001631	OMIM:610883	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610883	Potocki-Lupski syndrome		HP:0000303	PMID:17357070	PCS	HP:0003593				P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000303	PMID:17357070	PCS	HP:0003584				P	HPO:iea[2010-09-09]
OMIM:610883	Potocki-Lupski syndrome		HP:0000347	PMID:17357070	PCS	HP:0003593				P	HPO:iea[2010-09-09]
OMIM:275220	Tibial hemimelia		HP:0000924	OMIM:275220	IEA					P	HPO:iea[2009-02-17]
OMIM:275220	Tibial hemimelia		HP:0000007	OMIM:275220	IEA					I	HPO:iea[2009-02-17]
OMIM:275220	Tibial hemimelia		HP:0009556	OMIM:275220	TAS					P	HPO:skoehler[2013-10-22]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000142	OMIM:194072	TAS		HP:0040282			P	HPO:iea[2010-12-02];HPO:probinson[2025-09-26]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000112	OMIM:194072	TAS	HP:0003581				P	HPO:iea[2010-12-02];HPO:probinson[2025-09-26]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0001442	OMIM:194072	TAS					I	HPO:skoehler[2012-10-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000150	OMIM:194072	TAS		HP:0040283			P	HPO:iea[2010-12-02];HPO:probinson[2025-09-26]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000083	PMID:10945603	PCS	HP:0003581	10/46			P	HPO:iea[2009-02-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000130	OMIM:194072	TAS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2025-09-26]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0010464	OMIM:194072	TAS		HP:0040282			P	HPO:iea[2010-12-02];HPO:probinson[2025-09-26]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000526	OMIM:194072	TAS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0002667	OMIM:194072	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000047	OMIM:194072	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0001466	OMIM:194072	TAS					I	HPO:skoehler[2012-10-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000006	OMIM:194072	TAS					I	HPO:iea[2009-02-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0000028	OMIM:194072	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0001249	OMIM:194072	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194072	Wilms tumor, aniridia, genitourinary anomalies and impaired intellectual development syndrome		HP:0001513	OMIM:194072	TAS		4/20			P	HPO:iea[2010-12-02];HPO:iea[2009-02-17];HPO:probinson[2025-09-26]
OMIM:238320	Hypergonadotropic hypogonadism		HP:0000815	OMIM:238320	IEA					P	HPO:iea[2009-02-17]
OMIM:238320	Hypergonadotropic hypogonadism		HP:0000837	OMIM:238320	IEA					P	HPO:iea[2009-02-17]
OMIM:238320	Hypergonadotropic hypogonadism		HP:0000007	OMIM:238320	IEA					I	HPO:iea[2009-02-17]
OMIM:615723	Premature ovarian failure 8		HP:0008209	PMID:24597867	PCS		5/5			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0100615	PMID:24597867	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0011969	PMID:24597867	PCS		5/5			P	HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0011462	PMID:24597867	PCS		5/5			C	HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0008232	PMID:24597867	PCS		5/5			P	HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0000007	PMID:24597867	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0010464	PMID:24597867	PCS		5/5			P	HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0008214	PMID:24597867	PCS		5/5			P	HPO:probinson[2022-03-21]
OMIM:615723	Premature ovarian failure 8		HP:0000786	PMID:24597867	PCS		4/5			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-03-21]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000385	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0003577	PMID:21358632	PCS		1/1			C	HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000343	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0004322	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0002020	PMID:21358632	PCS	HP:0003593	1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0003090	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0001508	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0011342	PMID:21358632	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0012471	PMID:21358632	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0008551	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0030084	OMIM:613805	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000176	PMID:21358632	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000252	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000054	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0002750	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0003561	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0011968	PMID:21358632	PCS	HP:0003593	1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0005487	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0003100	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0003042	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0001263	PMID:21358632	PCS		1/1		HP:0012825	P	HPO:skoehler[2014-04-04];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0006361	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000327	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000007	PMID:21358632	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0006443	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0001511	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000028	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000369	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000347	PMID:21358632	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613805	Meier-Gorlin syndrome 5		HP:0000325	PMID:21358632	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000286	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000365	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000486	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001250	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001290	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0030939	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0011335	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0010442	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000319	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000954	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000316	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001007	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0002553	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000252	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000494	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000574	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0011968	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001263	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0100814	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000646	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000007	PMID:31209944	PCS					I	HPO:probinson[2020-08-26];HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0002307	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000369	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001655	PMID:31209944	PCS	HP:0003577	1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000126	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000384	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0003577	PMID:31209944	PCS					C	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000343	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001156	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000023	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000540	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0040082	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001508	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001629	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000219	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0002714	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000218	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0030084	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000411	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000179	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000154	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000396	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000431	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0002057	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000308	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000629	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0002205	PMID:31209944	PCS		3/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000664	PMID:31209944	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000543	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0001631	PMID:31209944	PCS		1/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000465	PMID:31209944	PCS		2/4			P	HPO:probinson[2020-08-26]
OMIM:618950	Suleiman-El-Hattab syndrome		HP:0000028	PMID:31209944	PCS		3/3	MALE		P	HPO:probinson[2020-08-26]
OMIM:309300	Megalocornea 1, X-linked		HP:0007836	PMID:22284829	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0001132	OMIM:309300	TAS					P	HPO:probinson[2012-07-25]
OMIM:309300	Megalocornea 1, X-linked		HP:0000483	OMIM:309300	TAS					P	HPO:probinson[2012-07-25]
OMIM:309300	Megalocornea 1, X-linked		HP:0000541	OMIM:309300	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:309300	Megalocornea 1, X-linked		HP:0000485	PMID:22284829	PCS	HP:0003577	16/16			P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0001084	PMID:22284829	PCS		10/16			P	HPO:probinson[2012-07-25];HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0012805	PMID:22284829	PCS		8/8			P	HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0012632	PMID:22284829	PCS		0/8			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:309300	Megalocornea 1, X-linked		HP:0100693	OMIM:309300	TAS					P	HPO:probinson[2012-07-25]
OMIM:309300	Megalocornea 1, X-linked		HP:0100689	PMID:22284829	PCS					P	HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0000518	PMID:22284829	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0001419	PMID:25712132	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0000616	OMIM:309300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:309300	Megalocornea 1, X-linked		HP:0007663	PMID:22284829	PCS		16/16			P	HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0007765	PMID:22284829	PCS					P	HPO:probinson[2019-07-14];HPO:probinson[2019-07-14]
OMIM:309300	Megalocornea 1, X-linked		HP:0000501	OMIM:309300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:177100	Pruritus, hereditary localized		HP:0003581	OMIM:177100	IEA					C	HPO:iea[2009-02-17]
OMIM:177100	Pruritus, hereditary localized		HP:0000989	OMIM:177100	IEA					P	HPO:iea[2009-02-17]
OMIM:177100	Pruritus, hereditary localized		HP:0001423	OMIM:177100	TAS					I	HPO:nvasilevsky[2019-02-28]
OMIM:177100	Pruritus, hereditary localized		HP:0000006	OMIM:177100	TAS					I	HPO:nvasilevsky[2019-02-28]
OMIM:300324	Intellectual developmental disorder, X-linked 53		HP:0001419	PMID:11337751	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2025-09-26]
OMIM:300324	Intellectual developmental disorder, X-linked 53		HP:0001249	PMID:11337751	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2025-09-26]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0003621	PMID:31298765	PCS		7/18			C	HPO:probinson[2023-03-23]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0011463	PMID:31298765	PCS		8/18			C	HPO:probinson[2023-03-23]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0011462	PMID:31298765	PCS		3/18			C	HPO:probinson[2023-03-23]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0007663	PMID:31298765	PCS					P	HPO:probinson[2023-03-23]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0000648	PMID:31298765	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-23]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0007843	PMID:31298765	PCS					P	HPO:probinson[2023-03-23]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0000512	PMID:31298765	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-23]
OMIM:165510	Optic atrophy with negative electroretinograms		HP:0000006	PMID:31298765	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-03-23]
OMIM:209300	ATRANSFERRINEMIA		HP:0001392	OMIM:209300	IEA					P	HPO:iea[2009-02-17]
OMIM:209300	ATRANSFERRINEMIA		HP:0012239	OMIM:209300	TAS					P	HPO:probinson[2013-04-01]
OMIM:209300	ATRANSFERRINEMIA		HP:0000007	OMIM:209300	TAS					I	HPO:probinson[2009-02-17]
OMIM:209300	ATRANSFERRINEMIA		HP:0001635	OMIM:209300	TAS					P	HPO:probinson[2009-02-17]
OMIM:209300	ATRANSFERRINEMIA		HP:0001931	OMIM:209300	TAS					P	HPO:probinson[2013-03-30]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000044	OMIM:244200	IEA					P	HPO:iea[2009-02-17]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000175	OMIM:244200	IEA					P	HPO:iea[2009-02-17]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000054	OMIM:244200	TAS					P	HPO:skoehler[2014-11-26]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000365	PMID:18559922	PCS		1/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000122	OMIM:244200	IEA					P	HPO:iea[2009-02-17]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0001250	PMID:18559922	PCS		1/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0032466	PMID:18559922	PCS		4/6			P	HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0006094	PMID:18559922	PCS		1/10			P	HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0003829	OMIM:244200	TAS					I	HPO:skoehler[2015-12-30]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000767	PMID:18559922	PCS		2/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000458	PMID:18559922	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000601	OMIM:244200	IEA					P	HPO:iea[2009-02-17]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0004409	PMID:18559922	PCS		5/10			P	HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0001335	PMID:18559922	PCS		2/10			P	HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0001763	PMID:18559922	PCS		3/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000006	OMIM:244200	TAS					I	HPO:skoehler[2015-12-30]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000204	OMIM:244200	IEA					P	HPO:iea[2009-02-17]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000028	PMID:18559922	PCS		2/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:244200	Hypogonadotropic hypogonadism 3 with or without anosmia		HP:0000786	OMIM:244200	TAS					P	HPO:skoehler[2014-11-26]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001058	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0003212	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0004322	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001890	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002240	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0003593	PMID:37349293	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0032435	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0011897	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0012311	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002718	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0025419	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001744	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0003623	PMID:37349293	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002573	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002650	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0006517	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001263	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0003261	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002590	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0012115	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0011227	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0012579	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002608	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0100614	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0000964	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0000007	PMID:37349293	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0004429	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002205	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001973	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001511	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001257	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002841	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002721	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0001974	PMID:37349293	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620565	Immunodeficiency 133 with autoimmunity and autoinflammation		HP:0002105	PMID:37349293	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0001684	PMID:31461301	PCS		1/2			P	HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0011968	PMID:31461301	PCS		1/1			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0000007	PMID:31461301	PCS					I	HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0006543	PMID:31461301	PCS		1/2			P	HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0012664	PMID:31461301	PCS		2/2			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0003811	PMID:31461301	PCS		2/2			C	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0002789	PMID:31461301	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0003623	PMID:31461301	PCS		2/2			C	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620203	Cardiomyopathy, dilated, 2H		HP:0011623	PMID:31461301	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:616969	Deafness, autosomal dominant 66		HP:0003577	PMID:26197441	PCS					C	HPO:probinson[2024-03-15]
OMIM:616969	Deafness, autosomal dominant 66		HP:0001751	PMID:26197441	IEA		0/11			P	HPO:probinson[2020-09-20];HPO:probinson[2024-03-15]
OMIM:616969	Deafness, autosomal dominant 66		HP:0000407	PMID:26197441	PCS		11/11			P	HPO:probinson[2017-06-25];HPO:probinson[2020-09-20]
OMIM:616969	Deafness, autosomal dominant 66		HP:0011463	PMID:26197441	PCS					C	HPO:probinson[2024-03-15]
OMIM:616969	Deafness, autosomal dominant 66		HP:0011462	PMID:26197441	PCS					C	HPO:probinson[2020-09-20]
OMIM:616969	Deafness, autosomal dominant 66		HP:0000006	PMID:26197441	PCS					I	HPO:probinson[2017-06-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0002850	PMID:31235509	PCS		2/2		HP:0012825	P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0001047	PMID:31235509	PCS		2/2			P	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0003212	PMID:31235509	PCS		2/2			P	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0030388	PMID:31235509	PCS					P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0030783	PMID:31235509	PCS		1/1			P	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0001581	PMID:31235509	PCS					P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0003593	PMID:31235509	PCS					C	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0033104	PMID:31235509	PCS					P	HPO:probinson[2020-10-13]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0032437	PMID:31235509	PCS					P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0031292	PMID:31235509	PCS					P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0100658	PMID:31235509	PCS		1/2			P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0000007	PMID:31235509	PCS					I	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0000403	PMID:31235509	PCS					P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0002788	PMID:31235509	PCS					P	HPO:probinson[2020-08-25]
OMIM:618944	Hyper-IgE recurrent infection syndrome 5, autosomal recessive		HP:0004315	PMID:31235509	PCS		2/2		HP:0012825	P	HPO:probinson[2020-08-25]
OMIM:212720	Martsolf syndrome 1		HP:0000286	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000044	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0006429	PMID:17394201	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0003992	OMIM:212720	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000486	PMID:17394201	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0001695	PMID:16532399	PCS		1/3			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0004322	OMIM:212720	IEA		1/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0004684	PMID:17394201	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0001252	PMID:16532399	PCS		2/3			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0030891	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0010049	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000518	PMID:17394201	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000519	PMID:16532399	PCS	HP:0003577	3/3			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000519	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0002938	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0002779	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0025336	PMID:16532399	PCS	HP:0003593	2/2			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0001840	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0001763	PMID:17394201;PMID:17515302	PCS		3/3			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000358	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0005743	PMID:17394201	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000494	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000252	PMID:17515302;PMID:16532399	PCS		3/4			P	HPO:probinson[2022-04-22];HPO:skoehler[2009-02-17];HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000054	PMID:16532399	PCS		2/2	MALE		P	HPO:skoehler[2009-02-17];HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000054	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0001264	PMID:16532399	PCS		2/2			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000692	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0001382	OMIM:212720	IEA					P	HPO:skoehler[2018-10-08]
OMIM:212720	Martsolf syndrome 1		HP:0001263	PMID:16532399	PCS		3/3			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000294	PMID:16532399	PCS		1/3			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000327	PMID:17515302	PCS		1/1		HP:0012825	P	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000767	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000007	PMID:16532399	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000568	PMID:16532399	PCS	HP:0003577	3/3			P	HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000568	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000768	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0004405	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000322	PMID:17394201	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0002943	PMID:17394201	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000248	PMID:17394201	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000369	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0002169	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000343	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000023	PMID:17394201	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0002162	PMID:17394201	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0010740	PMID:17394201	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0006094	PMID:17394201	PCS		2/2			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0008593	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0100702	PMID:17394201	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0008872	OMIM:212720	TAS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0002119	PMID:17394201	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000218	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000455	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0009803	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000750	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0004279	OMIM:212720	TAS					P	HPO:skoehler[2013-05-31]
OMIM:212720	Martsolf syndrome 1		HP:0001762	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0031936	PMID:17394201	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0011300	OMIM:212720	TAS					P	HPO:skoehler[2014-11-27]
OMIM:212720	Martsolf syndrome 1		HP:0011344	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0005280	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0100952	PMID:17394201	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0008388	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0001635	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0001638	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0002205	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0000028	PMID:16532399	PCS	HP:0003577	2/2	MALE		P	HPO:skoehler[2009-02-17];HPO:probinson[2021-07-10]
OMIM:212720	Martsolf syndrome 1		HP:0000028	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0000347	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212720	Martsolf syndrome 1		HP:0001315	PMID:17515302	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:212720	Martsolf syndrome 1		HP:0001831	OMIM:212720	IEA					P	HPO:skoehler[2009-02-17]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0000483	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0000486	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0001250	PMID:28779001	PCS		2/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0000020	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0001252	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002020	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0011951	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0040213	PMID:28779001	PCS	HP:0003623	3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0012850	PMID:28779001	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0012450	PMID:28779001	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0005968	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0001688	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0003623	PMID:28779001	PCS		3/3			C	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002015	PMID:28779001	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0031857	PMID:28779001	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002650	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0001288	PMID:28779001	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002791	PMID:28779001	PCS	HP:0003623	3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0011968	PMID:28779001	PCS	HP:0003623	3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002571	PMID:28779001	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0001263	PMID:28779001	PCS		2/2			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0001284	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002091	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0011471	PMID:28779001	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002808	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0000007	PMID:28779001	PCS					I	HPO:probinson[2021-09-22];HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0000545	PMID:28779001	PCS		1/3			P	HPO:probinson[2021-09-22]
OMIM:619482	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction		HP:0002104	PMID:28779001	PCS		3/3			P	HPO:probinson[2021-09-22]
OMIM:607864	Caudal duplication anomaly		HP:0003762	OMIM:612229	TAS					P	HPO:probinson[2013-09-15]
OMIM:607864	Caudal duplication anomaly		HP:0000073	OMIM:612229	TAS					P	HPO:probinson[2013-09-15]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0000253	OMIM:613811	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0002510	OMIM:613811	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0002169	OMIM:613811	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0002059	OMIM:613811	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0002079	OMIM:613811	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0001250	PMID:25044680	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0003121	OMIM:613811	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0001272	OMIM:613811	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0001263	PMID:25044680	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0003593	OMIM:613811	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0012448	OMIM:613811	TAS					P	HPO:skoehler[2013-11-28]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0002072	OMIM:613811	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0034353	PMID:25044680	PCS		3/3			P	HPO:probinson[2022-11-04]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0000737	OMIM:613811	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0033980	PMID:25044680	PCS		3/3			P	HPO:probinson[2022-11-04]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0000007	PMID:20920667	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-04]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0002518	OMIM:613811	TAS					P	HPO:skoehler[2013-06-05]
OMIM:613811	Pontocerebellar hypoplasia, type 2D		HP:0006855	PMID:25044680	PCS		3/3			P	HPO:probinson[2022-11-04]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000044	PMID:21855841	PCS		7/18			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0003676	OMIM:607694	TAS					C	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0003577	PMID:21855841	PCS		1/19			C	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000640	PMID:21855841	PCS		3/19			P	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0004322	OMIM:607694	TAS					P	HPO:skoehler[2015-11-15]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001332	OMIM:607694	TAS					P	HPO:skoehler[2015-11-15]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001310	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002120	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001272	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001250	PMID:21855841	PCS		3/19			P	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0003593	PMID:21855841	PCS		2/19			C	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001251	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000617	PMID:21855841	PCS		13/19			P	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0011463	PMID:21855841	PCS		6/19			C	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0003429	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002415	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000677	OMIM:607694	TAS					P	HPO:skoehler[2012-11-20]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001347	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000511	PMID:21855841	PCS		6/19			P	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0003621	PMID:21855841	PCS		10/19			C	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002015	PMID:21855841	PCS		7/19			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002079	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0003487	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002376	PMID:21855841	PCS		19/19			P	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001260	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001263	PMID:21855841	PCS		7/19			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002174	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0100613	PMID:21855841	PCS		3/19			C	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0009830	OMIM:607694	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000668	PMID:21855841	PCS		15/19			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000007	PMID:21855841	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000648	PMID:21855841	PCS		4/19			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002307	PMID:21855841	PCS		7/19			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000823	OMIM:607694	TAS		HP:0040281			P	HPO:skoehler[2015-11-15]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0002505	PMID:21855841	PCS		12/19			P	HPO:probinson[2022-04-24]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001257	OMIM:607694	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0000545	OMIM:607694	TAS					P	HPO:skoehler[2015-11-15]
OMIM:607694	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/orhypogonadotropic hypogonadism		HP:0001337	PMID:21855841	PCS		11/19			P	HPO:probinson[2022-04-24]
OMIM:616941	Agammaglobulinemia 8, autosomal dominant		HP:0004432	PMID:24216514	PCS		4/4			P	HPO:probinson[2017-06-25];HPO:probinson[2022-06-14]
OMIM:616941	Agammaglobulinemia 8, autosomal dominant		HP:0002719	PMID:24216514	PCS		4/4			P	HPO:probinson[2017-06-25];HPO:probinson[2022-06-14]
OMIM:616941	Agammaglobulinemia 8, autosomal dominant		HP:0003593	PMID:24216514	PCS		4/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14]
OMIM:616941	Agammaglobulinemia 8, autosomal dominant		HP:0000403	PMID:24216514	PCS		2/4			P	HPO:probinson[2017-06-25]
OMIM:616941	Agammaglobulinemia 8, autosomal dominant		HP:0010976	PMID:24216514	PCS		4/4			P	HPO:probinson[2017-06-25];HPO:probinson[2022-06-14]
OMIM:616941	Agammaglobulinemia 8, autosomal dominant		HP:0000006	PMID:24216514	PCS					I	HPO:probinson[2017-06-25]
OMIM:616941	Agammaglobulinemia 8, autosomal dominant		HP:0020090	OMIM:616941	TAS					P	HPO:probinson[2022-06-14]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0002089	OMIM:245650	IEA					P	HPO:iea[2009-02-17]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0012095	OMIM:245650	TAS					P	HPO:skoehler[2013-05-31]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0001373	OMIM:245650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0001939	OMIM:245650	IEA					P	HPO:iea[2009-02-17]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0008178	OMIM:245650	IEA					P	HPO:iea[2009-02-17]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0000007	OMIM:245650	IEA					I	HPO:iea[2009-02-17]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0010444	OMIM:245650	IEA					P	HPO:skoehler[2010-06-18]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0002779	OMIM:245650	IEA					P	HPO:iea[2009-02-17]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0002093	OMIM:245650	IEA					P	HPO:iea[2009-02-17]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0003811	OMIM:245650	IEA					C	HPO:iea[2009-02-17]
OMIM:245650	Larsen-like syndrome, Lethal type		HP:0001601	OMIM:245650	IEA					P	HPO:iea[2009-02-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0002421	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0000980	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0002121	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001252	OMIM:613839	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001251	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0002240	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0012448	OMIM:613839	TAS					P	HPO:skoehler[2013-11-28]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001290	OMIM:613839	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0012446	PMID:21310277	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001889	PMID:21310277	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0025435	PMID:21310277	PCS		1/3			P	HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0000952	OMIM:613839	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0002059	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0003621	PMID:21310277	PCS		1/3			C	HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001321	OMIM:613839	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0025097	OMIM:613839	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0011968	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001263	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0005484	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0011149	PMID:21310277	PCS		2/3			P	HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0040087	PMID:21310277	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0000007	PMID:21310277	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0005518	PMID:21310277	PCS		3/3			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001873	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency		HP:0001876	OMIM:613839	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001771	PMID:23664120	PCS		10/18			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003236	PMID:23664119	PCS		1/4			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003376	PMID:23664120	PCS		3/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0030973	PMID:23664120	PCS		12/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003691	PMID:23664119	PCS		11/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003273	PMID:23664120	PCS		2/18			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003593	PMID:23664119	PCS		2/12			C	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002380	PMID:23664119	PCS		2/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002061	PMID:23664120	PCS					P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001270	PMID:23664120	PCS		12/18			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003391	PMID:23664119	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0007340	PMID:23664120	PCS		18/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0011463	PMID:23664119	PCS		9/12			C	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0009046	PMID:23664119	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002515	PMID:23664119	PCS		12/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003307	PMID:23664119	PCS		9/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0007269	PMID:23664119	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003327	PMID:23664119	PCS		3/11			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001763	PMID:23664120	PCS		4/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001249	PMID:23664120	PCS		2/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001347	PMID:23664120	PCS		3/17			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003621	PMID:23664119	PCS		1/12			C	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001385	PMID:23664120	PCS	HP:0003577	5/18			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0011808	PMID:23664119	PCS		10/11			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002136	PMID:23664120	PCS		7/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001762	OMIM:615290	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002650	PMID:23664120	PCS		2/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002870	PMID:23664120	PCS		4/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001761	PMID:23664120	PCS		4/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0003487	PMID:23664120	PCS		5/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001283	PMID:23664120	PCS		1/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0001284	OMIM:615290	TAS				HP:0012839	P	HPO:skoehler[2013-10-06]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002091	PMID:23664120	PCS		1/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0009072	PMID:23664119	PCS		11/11			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0006380	PMID:23664120	PCS		3/18			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0009053	PMID:23664119	PCS		2/11			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002808	PMID:23664120	PCS		1/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0007210	PMID:23664120	PCS		13/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0000767	PMID:23664120	PCS		1/18			P	HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0030051	OMIM:615290	TAS					P	HPO:skoehler[2014-11-27]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0000006	PMID:23664119	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-08-05]
OMIM:615290	Spinal muscular atrophy, lower extremity-predominant, 2, autosomaldominant		HP:0002600	PMID:23664120	PCS		9/17			P	HPO:probinson[2022-08-05]
OMIM:208750	Ataxia, deafness, and cardiomyopathy		HP:0000407	OMIM:208750	IEA					P	HPO:iea[2009-02-17]
OMIM:208750	Ataxia, deafness, and cardiomyopathy		HP:0001251	OMIM:208750	IEA					P	HPO:iea[2009-02-17]
OMIM:208750	Ataxia, deafness, and cardiomyopathy		HP:0000007	OMIM:208750	IEA					I	HPO:iea[2009-02-17]
OMIM:208750	Ataxia, deafness, and cardiomyopathy		HP:0001638	OMIM:208750	IEA					P	HPO:iea[2009-02-17]
OMIM:208750	Ataxia, deafness, and cardiomyopathy		HP:0001249	OMIM:208750	IEA					P	HPO:iea[2009-02-17]
OMIM:208750	Ataxia, deafness, and cardiomyopathy		HP:0000951	OMIM:208750	IEA					P	HPO:iea[2009-02-17]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0003577	PMID:22958903	PCS		6/6			C	HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0007260	PMID:22958903	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0001321	PMID:22958903	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0001263	PMID:22958903	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0001252	PMID:22958903	PCS		3/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0003560	PMID:22958903	PCS		6/6			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0000007	PMID:22958903	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0000238	PMID:22958903	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0000568	PMID:22958903	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0002119	PMID:22958903	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0007973	PMID:22958903	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:614830	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8		HP:0000501	PMID:22958903	PCS		2/6			P	HPO:probinson[2023-02-12]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000341	PMID:28805828	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0003774	PMID:28805828	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001310	PMID:28805828	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000100	PMID:28805828	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0004322	PMID:28805828	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001272	PMID:28805828	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001250	PMID:28805828	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001252	PMID:28805828	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0003593	PMID:28805828	PCS		2/3			C	HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000639	PMID:28805828	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0011463	PMID:28805828	PCS		1/3			C	HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000218	PMID:28805828	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001249	PMID:28805828	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001166	PMID:28805828	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0002059	PMID:28805828	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000750	OMIM:301006	IEA					P	HPO:skoehler[2018-10-08]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0002650	PMID:28805828	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0011968	PMID:28805828	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001263	PMID:28805828	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000097	PMID:28805828	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000093	PMID:28805828	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0012579	PMID:28805828	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001419	PMID:28805828	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0011451	PMID:28805828	PCS		3/3			P	HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000565	OMIM:301006	IEA					P	HPO:skoehler[2018-10-08]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001511	PMID:28805828	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0001257	PMID:28805828	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0000347	PMID:28805828	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:301006	Galloway-Mowat syndrome 2, X-linked		HP:0002126	PMID:28805828	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:601583	Wilms tumor 5		HP:0001442	OMIM:601583	IEA					I	HPO:iea[2009-02-17]
OMIM:601583	Wilms tumor 5		HP:0002667	OMIM:601583	IEA					P	HPO:iea[2009-02-17]
OMIM:601583	Wilms tumor 5		HP:0000006	OMIM:601583	IEA					I	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000044	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000054	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0001341	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000771	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0001761	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000122	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0030344	PMID:6604133	PCS					P	HPO:probinson[2017-08-12]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0003782	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0001251	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0003164	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0030341	PMID:6604133	PCS					P	HPO:probinson[2017-08-12]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0002929	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000458	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000029	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000218	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0001417	OMIM:308750	IEA					I	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0001335	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0001258	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0000028	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:308750	Kallmann syndrome with spastic paraplegia		HP:0002225	OMIM:308750	IEA					P	HPO:iea[2009-02-17]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0012265	PMID:19944400	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0001696	PMID:19944400;PMID:19944405	PCS	HP:0003577	5/8			P	HPO:probinson[2022-03-05];HPO:probinson[2013-01-09];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0012256	PMID:19944400;PMID:19944405	PCS		8/8			P	HPO:probinson[2022-03-05];HPO:probinson[2013-06-02];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0002110	PMID:19944405	PCS		5/5			P	HPO:probinson[2013-06-02];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0012263	PMID:19944400;PMID:19944405	PCS		8/8			P	HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0000789	PMID:19944405	PCS		2/2			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0002837	PMID:19944405	PCS		5/5			P	HPO:probinson[2013-06-02];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0000403	PMID:19944405	PCS		3/5			P	HPO:probinson[2013-06-02];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0000007	PMID:19944400	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0012257	PMID:19944400;PMID:19944405	PCS		8/8			P	HPO:probinson[2022-03-05];HPO:probinson[2013-06-02];HPO:probinson[2022-03-05]
OMIM:613193	Ciliary dyskinesia, primary, 13		HP:0011108	PMID:19944405	PCS		4/5			P	HPO:probinson[2022-03-05]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0003202	PMID:23749797	PCS		3/3			P	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0004336	PMID:23749797	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0003621	PMID:23749797	PCS		3/3			C	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0000252	OMIM:615284	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0003676	OMIM:615284	TAS					C	HPO:skoehler[2013-10-06]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0002650	PMID:23749797;OMIM:615284	PCS		12/13			P	HPO:probinson[2022-11-02];HPO:skoehler[2013-10-06]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0000486	OMIM:615284	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0001288	OMIM:615284	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0003484	PMID:23749797	PCS		3/3			P	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0003383	PMID:23749797;OMIM:615284	PCS		11/11			P	HPO:probinson[2022-11-02];HPO:skoehler[2013-10-06]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0000020	OMIM:615284	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0001284	PMID:23749797	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0012444	OMIM:615284	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0010546	PMID:23749797	PCS		3/3			P	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0009053	PMID:23749797	PCS	HP:0003621	3/3			P	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0007340	PMID:23749797	PCS		3/3			P	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0000602	OMIM:615284	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0000007	PMID:23749797	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0002936	PMID:23749797	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0002505	PMID:23749797	PCS	HP:0003596	2/3			P	HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0001159	OMIM:615284	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0000762	PMID:23749797	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0001763	PMID:23749797	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-11-02]
OMIM:615284	Charcot-Marie-Tooth disease, type 4B3		HP:0001249	PMID:23749797	PCS		0/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-11-02]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0002014	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0002188	PMID:31395333	PCS		2/9			P	HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0002013	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0004322	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001250	PMID:31395333	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:6000355	PMID:9869665	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001252	PMID:31395333	PCS		6/9			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001263	PMID:31395333	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001290	PMID:31395333	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0033213	PMID:3709568	PCS					P	HPO:probinson[2020-10-12]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0011664	PMID:31395333	PCS		1/9			P	HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0012450	OMIM:248360	TAS					P	HPO:skoehler[2013-11-28]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0012120	PMID:31395333	PCS					P	HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0000007	PMID:31395333	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001943	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001946	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001302	OMIM:248360	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0002019	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001942	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0002027	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0002643	PMID:31395333	PCS	HP:0003623	3/9			P	HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001249	PMID:31395333	PCS		5/6			P	HPO:probinson[2020-10-13]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0003128	OMIM:248360	IEA					P	HPO:iea[2009-02-17]
OMIM:248360	Malonyl-CoA decarboxylase deficiency		HP:0001644	PMID:31395333	PCS		5/9			P	HPO:probinson[2020-10-13]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002487	OMIM:617493	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002421	PMID:25966631	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002069	PMID:25966631	PCS		1/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002188	PMID:25966631	PCS		1/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0001332	OMIM:617493	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002384	PMID:25966631	PCS		3/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0001272	PMID:25966631	PCS		1/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0003593	PMID:25966631	PCS		3/4			C	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0001290	OMIM:617493	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0010841	PMID:25966631	PCS		2/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0012469	PMID:25966631	PCS		1/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0007366	PMID:25966631	PCS		1/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002119	OMIM:617493	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0003623	PMID:25966631	PCS		1/4			C	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002059	PMID:25966631	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002015	OMIM:617493	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0000252	OMIM:617493	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0001344	PMID:25966631	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002079	PMID:25966631	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002310	OMIM:617493	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0001263	PMID:25966631	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002072	PMID:25966631	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0100660	OMIM:617493	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0100716	OMIM:617493	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0200134	PMID:25966631	PCS		2/4			P	HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0002305	PMID:25966631	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0001257	OMIM:617493	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0000006	PMID:25966631	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28]
OMIM:617493	Neurodevelopmental disorder with involuntary movements		HP:0004305	PMID:25966631	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:101900	Acrokeratosis verruciformis		HP:0003577	PMID:12542527	PCS		2/2			C	HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0001807	PMID:12542527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0200016	PMID:12542527	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0025092	PMID:12542527	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0007530	PMID:12542527	PCS					P	HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0012500	PMID:12542527	PCS					P	HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0000006	PMID:12542527	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0100792	PMID:12542527	PCS		0/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-09]
OMIM:101900	Acrokeratosis verruciformis		HP:0000962	PMID:12542527	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:609646	Deafness, neurosensory, autosomal recessive 42		HP:0000407	OMIM:609646	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609646	Deafness, neurosensory, autosomal recessive 42		HP:0003680	OMIM:609646	IEA					C	HPO:iea[2009-02-17]
OMIM:609646	Deafness, neurosensory, autosomal recessive 42		HP:0003593	OMIM:609646	IEA					C	HPO:iea[2009-02-17]
OMIM:609646	Deafness, neurosensory, autosomal recessive 42		HP:0000007	OMIM:609646	IEA					I	HPO:iea[2009-02-17]
OMIM:179850	Dowling-Degos disease		HP:0007456	OMIM:179850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:179850	Dowling-Degos disease		HP:0000006	OMIM:179850	TAS					I	HPO:skoehler[2009-02-17]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000384	PMID:27040691	PCS		1/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000083	OMIM:617478	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0011611	PMID:28318500	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0031664	PMID:27040691	PCS		4/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0011662	PMID:28318500	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001629	PMID:28318500	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001845	PMID:27040691	PCS		1/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001522	PMID:27040691	PCS		3/4			C	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000252	PMID:28318500	PCS	HP:0003623	1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001660	PMID:28318500	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0005301	PMID:28318500	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0010773	PMID:28318500	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0012020	PMID:28318500	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0007430	PMID:28318500	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000107	PMID:28318500	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001636	PMID:28318500	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001999	PMID:27040691	PCS		1/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000007	PMID:28318500	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001338	PMID:28318500	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001319	PMID:27040691	PCS	HP:0003623	1/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000961	PMID:27040691	PCS		2/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0001631	PMID:28318500	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000465	PMID:27040691	PCS		1/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0000369	PMID:27040691	PCS		1/4			P	HPO:probinson[2019-09-03]
OMIM:617478	Structural heart defects and renal anomalies syndrome		HP:0003259	PMID:27040691	PCS	HP:0003593	3/3			P	HPO:probinson[2019-09-03]
OMIM:166970	Ovarian fibromata		HP:0010618	OMIM:166970	IEA					P	HPO:skoehler[2009-02-17]
OMIM:166970	Ovarian fibromata		HP:0000006	OMIM:166970	IEA					I	HPO:iea[2009-02-17]
OMIM:143500	Gilbert syndrome		HP:0008282	PMID:11316168	PCS		20/20			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-13]
OMIM:143500	Gilbert syndrome		HP:0001399	PMID:11316168	PCS		0/20			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-13]
OMIM:143500	Gilbert syndrome		HP:0000007	PMID:10412811	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:143500	Gilbert syndrome		HP:0002910	PMID:11316168	PCS		0/20			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:143500	Gilbert syndrome		HP:0000952	OMIM:143500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0030402	PMID:22461475	PCS		0/1			P	HPO:probinson[2022-09-25]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0001882	PMID:22461475	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0000639	PMID:22461475	PCS	HP:0003577	1/1			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-09-25]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0001010	OMIM:614171	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0001263	PMID:22461475	PCS		0/1			P	HPO:probinson[2022-09-25]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0001581	PMID:22461475	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0000007	PMID:22461475	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0007894	OMIM:614171	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0001107	PMID:22461475	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614171	Hermansky-Pudlak syndrome 9		HP:0001873	PMID:22461475	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:614617	Deafness, autosomal recessive 86		HP:0003577	PMID:24387994	PCS					C	HPO:probinson[2022-11-06]
OMIM:614617	Deafness, autosomal recessive 86		HP:0000365	PMID:24387994	PCS		11/11			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-11-06]
OMIM:614617	Deafness, autosomal recessive 86		HP:0000007	PMID:24387994	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0003577	PMID:33963192	PCS		7/29			C	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0003676	PMID:33963192	PCS		6/28			C	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0000750	PMID:33963192	PCS		26/27			P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0002540	PMID:33963192	PCS		8/27			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0001272	PMID:33963192	PCS		30/30			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0001263	PMID:33963192	PCS		30/30			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0001252	PMID:33963192	PCS		26/29			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0003593	PMID:33963192	PCS		21/30			C	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0001251	PMID:33963192	PCS		19/27			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0001284	PMID:33963192	PCS		4/25			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0001270	PMID:33963192	PCS		30/30			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0012389	PMID:33963192	PCS		13/29			P	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0011463	PMID:33963192	PCS		1/29			C	HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0000007	PMID:33963192	PCS					I	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:619333	Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction		HP:0001348	PMID:33963192	PCS		15/25			P	HPO:probinson[2021-06-26]
OMIM:616000	Analbuminemia		HP:0001562	PMID:23730173	PCS	HP:0011461	3/11			P	HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0002783	PMID:23730173	PCS		6/11			P	HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0003124	PMID:8621984	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0003141	PMID:29981851	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0001263	PMID:23730173	PCS		2/11			P	HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0003073	PMID:29981851;PMID:11781148;PMID:8621984;PMID:23730173	PCS		16/16			P	HPO:probinson[2021-05-31];HPO:skoehler[2015-09-15];HPO:probinson[2020-07-21];HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0012378	PMID:29981851	PCS		2/2			P	HPO:skoehler[2015-09-15];HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0000939	PMID:8621984	PCS		2/2			P	HPO:skoehler[2015-09-15];HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0000969	PMID:29981851	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0032386	PMID:29981851	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0000007	PMID:11781148	PCS					I	HPO:skoehler[2015-09-15];HPO:probinson[2020-07-21]
OMIM:616000	Analbuminemia		HP:0009125	PMID:29981851	PCS		1/2			P	HPO:skoehler[2015-09-15];HPO:probinson[2021-05-31]
OMIM:616000	Analbuminemia		HP:0002615	OMIM:616000	TAS					P	HPO:skoehler[2015-09-15]
OMIM:616000	Analbuminemia		HP:0001643	PMID:23730173	PCS		2/11			P	HPO:probinson[2021-05-31]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0004324	PMID:34113521	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0003621	PMID:32505587	PCS		1/1			C	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0000365	OMIM:274300	IEA					P	HPO:iea[2009-02-17]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0031506	PMID:32505587	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0025379	PMID:34113521	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0032069	PMID:34113521;PMID:32505587	PCS		1/2			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0012378	PMID:34113521	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0010655	OMIM:274300	IEA					P	HPO:iea[2009-02-17]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0000819	PMID:34113521	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0033077	PMID:32505587	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0001518	OMIM:274300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0034189	PMID:34113521;PMID:32505587	PCS		1/2			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0000007	PMID:1991834	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0008223	PMID:34113521	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0002925	PMID:34113521;PMID:32505587	PCS		1/2			P	HPO:probinson[2022-04-22];HPO:probinson[2022-04-22];HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0007018	PMID:32505587	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0000520	OMIM:274300	IEA					P	HPO:iea[2009-02-17]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0005978	PMID:34113521	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0000853	PMID:32505587	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:274300	Thyroid hormone resistance, generalized, autosomal recessive		HP:0002930	OMIM:274300	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0003355	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0001252	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0002240	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0001290	OMIM:239200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0003072	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0001508	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0001903	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0008872	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0002757	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0003109	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0000774	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0002019	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0001744	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0003761	OMIM:239200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0003025	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0003165	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0002094	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0002150	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0001959	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0008200	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0000007	OMIM:239200	TAS					I	HPO:skoehler[2017-07-13]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0000103	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0002789	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0002148	OMIM:239200	IEA					P	HPO:iea[2009-02-17]
OMIM:239200	Hyperparathyroidism, neonatal severe		HP:0000006	OMIM:239200	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614165	Paragangliomas 5		HP:0002668	PMID:23750034;PMID:20484225	PCS		2/2			P	HPO:probinson[2021-02-20];HPO:skoehler[2015-01-27];HPO:probinson[2021-02-20]
OMIM:614165	Paragangliomas 5		HP:0000006	PMID:20484225	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:270600	Spastic diplegia, Infantile type		HP:0001264	OMIM:270600	IEA					P	HPO:iea[2009-02-17]
OMIM:270600	Spastic diplegia, Infantile type		HP:0003593	OMIM:270600	IEA					C	HPO:iea[2009-02-17]
OMIM:270600	Spastic diplegia, Infantile type		HP:0000007	OMIM:270600	IEA					I	HPO:iea[2009-02-17]
OMIM:270600	Spastic diplegia, Infantile type		HP:0001249	OMIM:270600	IEA					P	HPO:iea[2009-02-17]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0002850	PMID:25512081	PCS		2/2			P	HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0001531	PMID:25512081	PCS	HP:0003593	1/2			P	HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0001025	PMID:25512081	PCS	HP:0003621	1/2			P	HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0025289	PMID:25512081	PCS					P	HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0000007	PMID:25512081	PCS					I	HPO:probinson[2020-09-08];HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0002205	PMID:25512081	PCS	HP:0003593	2/2			P	HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0010976	PMID:25512081	PCS		2/2			P	HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0031545	PMID:25512081	PCS		2/2			P	HPO:probinson[2020-09-08]
OMIM:618987	Immunodeficiency 73C with defective neutrophil chemotaxis and hypogammaglobulinemia		HP:0004315	PMID:25512081	PCS		2/2			P	HPO:probinson[2020-09-08]
OMIM:619441	Encephalitis, acute, infection (viral)-induced, susceptibility to, 11		HP:0003621	PMID:29474921	PCS		3/7			C	HPO:probinson[2021-08-21]
OMIM:619441	Encephalitis, acute, infection (viral)-induced, susceptibility to, 11		HP:0011342	PMID:29474921	PCS	HP:0003593	1/7			P	HPO:probinson[2021-08-21]
OMIM:619441	Encephalitis, acute, infection (viral)-induced, susceptibility to, 11		HP:0011463	PMID:29474921	PCS		2/7			C	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619441	Encephalitis, acute, infection (viral)-induced, susceptibility to, 11		HP:0003593	PMID:29474921	PCS		2/7			C	HPO:probinson[2021-08-21]
OMIM:619441	Encephalitis, acute, infection (viral)-induced, susceptibility to, 11		HP:0000007	PMID:29474921	PCS					I	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619441	Encephalitis, acute, infection (viral)-induced, susceptibility to, 11		HP:0033993	PMID:29474921	PCS	HP:0003621	7/7			P	HPO:probinson[2021-10-03]
OMIM:619441	Encephalitis, acute, infection (viral)-induced, susceptibility to, 11		HP:0001511	PMID:29474921	PCS	HP:0011461	1/7			P	HPO:probinson[2021-08-21]
OMIM:600110	Stargardt disease 3		HP:0011507	PMID:11138005	PCS					P	HPO:probinson[2012-07-18];HPO:probinson[2021-07-07]
OMIM:600110	Stargardt disease 3		HP:0007663	PMID:11138005	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2021-07-07]
OMIM:600110	Stargardt disease 3		HP:0000505	PMID:11138005	PCS					P	HPO:probinson[2012-07-18];HPO:probinson[2021-07-07]
OMIM:600110	Stargardt disease 3		HP:0007401	PMID:11138005	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-07]
OMIM:600110	Stargardt disease 3		HP:0007754	PMID:11138005	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-07]
OMIM:600110	Stargardt disease 3		HP:0000006	PMID:11138005	PCS					I	HPO:probinson[2012-07-18];HPO:probinson[2021-07-07]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0000750	OMIM:300495	IEA					P	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0002353	OMIM:300495	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0002332	OMIM:300495	IEA					P	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0001250	PMID:14963808	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0003144	OMIM:300495	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0011463	OMIM:300495	IEA					C	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0000729	PMID:14963808;PMID:12669065	PCS		4/10			P	HPO:probinson[2021-09-25]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0000723	OMIM:300495	TAS					P	HPO:skoehler[2013-06-04]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0001426	OMIM:300495	IEA					I	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0000733	OMIM:300495	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0000758	OMIM:300495	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0001417	PMID:12669065	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0003745	OMIM:300495	IEA					I	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0001357	PMID:14963808	PCS		2/5			P	HPO:probinson[2021-09-25]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0000732	OMIM:300495	IEA					P	HPO:iea[2009-02-17]
OMIM:300495	Autism, susceptibility to, X-linked 2		HP:0000721	OMIM:300495	IEA					P	HPO:iea[2009-02-17]
OMIM:600138	Retinitis pigmentosa 11		HP:0001133	PMID:20939871	PCS					P	HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0007737	PMID:17325180	PCS					P	HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0000662	PMID:20939871	PCS		5/6			P	HPO:skoehler[2015-12-30];HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0030629	PMID:20939871	PCS		4/6			P	HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0040049	PMID:17325180	PCS		4/6			P	HPO:skoehler[2014-11-26];HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0000608	OMIM:600138	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:600138	Retinitis pigmentosa 11		HP:0003829	PMID:23041261	PCS					I	HPO:skoehler[2014-03-24];HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0000618	OMIM:600138	TAS					P	HPO:skoehler[2015-12-30]
OMIM:600138	Retinitis pigmentosa 11		HP:0007663	PMID:20939871	PCS					P	HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0007401	OMIM:600138	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:600138	Retinitis pigmentosa 11		HP:0000510	PMID:20939871	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0000543	PMID:20939871	PCS		2/6			P	HP:probinson[2019-03-01]
OMIM:600138	Retinitis pigmentosa 11		HP:0000006	PMID:17325180	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0003037	PMID:22587682	PCS		5/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0003577	PMID:22587682	PCS		5/5			C	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000023	OMIM:607131	TAS					P	HPO:skoehler[2015-08-16]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0001274	OMIM:607131	TAS					P	HPO:skoehler[2015-08-16]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0001270	OMIM:607131	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0003071	PMID:22587682	PCS		5/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0010442	PMID:22587682	PCS		0/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0012444	OMIM:607131	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000316	PMID:22587682	PCS		4/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0002419	PMID:22587682	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0030084	PMID:22587682	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0002857	PMID:22587682	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0002656	PMID:22587682	PCS		5/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0001004	PMID:22587682	PCS		2/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000256	PMID:22587682	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0002654	OMIM:607131	IEA					P	HPO:skoehler[2015-01-27]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000431	PMID:22587682	PCS		5/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0002079	PMID:22587682	PCS		3/4			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0001263	PMID:22587682	PCS		4/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000272	PMID:22587682	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000470	PMID:22587682	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0001182	PMID:22587682	PCS		5/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0005280	PMID:22587682	PCS		5/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0001999	OMIM:607131	IEA					P	HPO:skoehler[2015-01-19]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000767	PMID:22587682	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000007	PMID:22587682	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000768	OMIM:607131	TAS					P	HPO:skoehler[2015-08-16]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000207	PMID:22587682	PCS		4/5			P	HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0002007	PMID:22587682	PCS		5/5			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-06]
OMIM:607131	Al-Gazali-Bakalinova syndrome		HP:0000369	PMID:22587682	PCS		5/5			P	HPO:probinson[2022-11-06]
OMIM:618011	Hyperekplexia 4		HP:0001276	PMID:28180185	PCS		2/2			P	HPO:probinson[2018-06-12];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0001298	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0002751	OMIM:618011	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618011	Hyperekplexia 4		HP:0002521	PMID:28180185	PCS		1/2			P	HPO:probinson[2018-06-12];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0003577	PMID:28180185	PCS		2/2			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0003676	PMID:28180185	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0002059	OMIM:618011	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0001762	OMIM:618011	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618011	Hyperekplexia 4		HP:0000023	PMID:28180185	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0001250	PMID:28180185	PCS		2/2			P	HPO:probinson[2018-06-12];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0001371	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0005684	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0001263	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0001181	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0012469	PMID:28180185	PCS		0/1			P	HPO:probinson[2018-06-12];HPO:probinson[2024-03-15]
OMIM:618011	Hyperekplexia 4		HP:0012385	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0001537	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618011	Hyperekplexia 4		HP:0000007	PMID:28180185	PCS					I	HPO:probinson[2018-06-12]
OMIM:618011	Hyperekplexia 4		HP:0002878	PMID:28180185	PCS		2/2			P	HPO:probinson[2018-06-12];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0012071	PMID:28180185	PCS		0/1			P	HPO:probinson[2024-03-15]
OMIM:618011	Hyperekplexia 4		HP:0000218	OMIM:618011	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618011	Hyperekplexia 4		HP:0001347	PMID:28180185	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:618011	Hyperekplexia 4		HP:0001336	OMIM:618011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0100018	OMIM:600886	IEA					P	HPO:iea[2009-02-17]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0040135	PMID:15280904	PCS		0/7			P	HPO:skoehler[2015-01-04];HP:probinson[2019-03-01];HPO:probinson[2024-03-09]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0012464	PMID:23421845	PCS		1/7			P	HPO:probinson[2024-03-09]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0010923	PMID:15280904	PCS		7/7			P	HPO:probinson[2024-03-09]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0000518	PMID:23421845	PCS		6/8			P	HPO:probinson[2024-03-09]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0010693	OMIM:600886	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0003581	PMID:23421845	PCS		8/8			C	HPO:probinson[2024-03-09]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0040130	PMID:23421845	PCS		0/8			P	HPO:skoehler[2015-01-04];HP:probinson[2019-03-01];HPO:probinson[2024-03-09]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0003281	PMID:15280904;PMID:23421845	PCS		15/15			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01];HPO:probinson[2024-03-09]
OMIM:600886	Hyperferritinemia with or without cataract		HP:0000006	PMID:15280904	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0003676	PMID:26078401	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0003621	PMID:26078401	PCS		3/3			C	HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0003431	PMID:26078401	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0001761	OMIM:605726	IEA					P	HPO:iea[2009-02-17]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0003487	PMID:26078401	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0003693	PMID:26078401	PCS		3/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0002460	PMID:26078401	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0034337	PMID:26078401	PCS		1/3			P	HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0007083	PMID:26078401	PCS		3/3			P	HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0033383	PMID:26078401	PCS		1/1			P	HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0009027	PMID:26078401	PCS		3/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0000007	PMID:26078401	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0007269	PMID:26078401	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0003438	PMID:26078401	PCS		3/3			P	HPO:probinson[2023-01-16]
OMIM:605726	Spinal muscular atrophy, distal, autosomal recessive, 2		HP:0001765	OMIM:605726	TAS					P	HPO:skoehler[2015-11-15]
OMIM:613144	Choroidal dystrophy, central areolar 3		HP:0011510	PMID:19696794	PCS		6/21			P	HPO:skoehler[2012-11-18]
OMIM:613144	Choroidal dystrophy, central areolar 3		HP:0000006	OMIM:613144	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613144	Choroidal dystrophy, central areolar 3		HP:0000533	PMID:19696794	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0003236	PMID:15894594	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0003577	PMID:15894594	PCS		3/3			C	HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0009917	PMID:15894594	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000540	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0002365	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0001250	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0006829	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0001274	PMID:15894594	IEA		1/3			P	HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0002084	OMIM:613150	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0007260	PMID:15894594	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000518	PMID:15894594	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000557	PMID:15894594	PCS		2/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000238	PMID:15894594	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000659	PMID:15894594	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0002119	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000158	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0001302	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0001522	PMID:15894594	IEA		2/3			C	HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0003306	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0002951	PMID:15894594	IEA		1/3			P	HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000175	PMID:15894594	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000252	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0002650	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0001321	PMID:15894594	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0002350	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0003560	PMID:15894594	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0007033	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0002803	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000007	PMID:15894594	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000568	PMID:15894594	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0003712	OMIM:613150	TAS					P	HPO:skoehler[2012-11-18]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000204	PMID:15894594	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-09]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000501	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0000545	OMIM:613150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		HP:0003557	PMID:15894594	IEA		1/1			P	HPO:probinson[2021-05-09]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0010628	PMID:28017374	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0003621	PMID:28017374	PCS		2/4			C	HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0001762	PMID:28017374	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0003596	PMID:28017374	PCS		1/4			C	HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0001761	PMID:28017374	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0002792	PMID:28017374	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0011705	PMID:28017374	PCS		1/4			P	HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0003691	PMID:28017374	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0003391	PMID:28017374	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0040081	PMID:28017374	PCS		0/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0011463	PMID:28017374	PCS		1/4			C	HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0000767	PMID:28017374	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0000007	PMID:28017374	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0001638	PMID:28017374	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0002515	PMID:28017374	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0000218	PMID:28017374	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0003803	PMID:28017374	PCS		4/4			P	HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0001324	PMID:28017374	PCS		4/4			P	HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0003798	PMID:28017374	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-29]
OMIM:617336	Nemaline myopathy 11, autosomal recessive		HP:0003677	PMID:28017374	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000341	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000121	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0003577	PMID:29304374	PCS		3/3			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0004322	PMID:29304374	PCS		3/3			P	HPO:skoehler[2019-04-18]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0002783	PMID:29304374	PCS		1/3			P	HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001250	PMID:29304374	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0003196	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001252	PMID:29304374	PCS		3/3			P	HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001508	PMID:29304374	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000938	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000337	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000557	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001943	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000218	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001643	PMID:29304374	PCS		1/3			P	HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000278	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001007	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001249	PMID:29304374	PCS		3/3			P	HPO:skoehler[2018-10-08]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0002751	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0009826	PMID:29304374	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000252	PMID:29304374	PCS		3/3			P	HPO:skoehler[2019-04-18]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001561	PMID:29304374	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000431	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0011968	PMID:29304374	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0011344	PMID:29304374	PCS		3/3			P	HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0034392	PMID:29304374	PCS		1/3			P	HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0002827	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000007	PMID:29304374	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000821	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000348	PMID:29304374	PCS		1/3			P	HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001511	PMID:29304374	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001631	PMID:29304374	PCS		1/3			P	HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0000501	PMID:29304374	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:618005	Congenital disorder of glycosylation with defective fucosylation 1		HP:0001875	PMID:29304374	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:616028	Adams-Oliver syndrome 5		HP:0003577	PMID:25132448	PCS		6/6			C	HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001971	OMIM:616028	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001057	PMID:25132448	PCS		5/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001156	PMID:25132448	PCS		2/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0000023	PMID:25132448	PCS		1/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001250	PMID:25132448	PCS		1/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0030242	PMID:25132448	PCS		1/6			P	HPO:skoehler[2015-01-20];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0002040	OMIM:616028	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:616028	Adams-Oliver syndrome 5		HP:0030718	OMIM:616028	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616028	Adams-Oliver syndrome 5		HP:0002092	PMID:25132448	PCS		1/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001537	PMID:25132448	PCS		1/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0025107	PMID:25132448	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001800	PMID:25132448	PCS		1/6			P	HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001802	PMID:25132448	PCS		2/6			P	HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001159	PMID:25132448	PCS		2/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001048	OMIM:616028	TAS					P	HPO:skoehler[2014-10-06]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001642	PMID:25132448	PCS		1/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0000006	PMID:25132448	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-05]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001810	OMIM:616028	TAS					P	HPO:skoehler[2014-10-06]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001667	OMIM:616028	TAS					P	HPO:skoehler[2014-10-06]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001744	OMIM:616028	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:616028	Adams-Oliver syndrome 5		HP:0001655	OMIM:616028	IEA					P	HPO:skoehler[2018-10-08]
OMIM:166780	Otofaciocervical syndrome		HP:0000275	PMID:16441263	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0000472	OMIM:166780	IEA					P	HPO:iea[2009-02-17]
OMIM:166780	Otofaciocervical syndrome		HP:0004467	OMIM:166780	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0000276	PMID:16441263	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0000460	OMIM:166780	IEA					P	HPO:iea[2009-02-17]
OMIM:166780	Otofaciocervical syndrome		HP:0003691	OMIM:166780	IEA					P	HPO:iea[2009-02-17]
OMIM:166780	Otofaciocervical syndrome		HP:0008586	PMID:16441263	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0000405	OMIM:166780	IEA					P	HPO:iea[2009-02-17]
OMIM:166780	Otofaciocervical syndrome		HP:0000218	PMID:16441263	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0000378	PMID:16441263	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0200021	PMID:16441263	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0000410	PMID:16441263	IEA		1/1			P	HPO:probinson[2022-04-24]
OMIM:166780	Otofaciocervical syndrome		HP:0000006	PMID:16441263	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:131800	Epidermolysis bullosa simplex, Weber-Cockayne type		HP:0001056	PMID:9284105	PCS		0/33			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-12]
OMIM:131800	Epidermolysis bullosa simplex, Weber-Cockayne type		HP:0011463	PMID:9284105	PCS		33/33			C	HPO:probinson[2022-05-12]
OMIM:131800	Epidermolysis bullosa simplex, Weber-Cockayne type		HP:0007446	PMID:7506606;PMID:17039244;PMID:9284105;PMID:27283507	PCS		59/59			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-12];HPO:probinson[2022-05-12]
OMIM:131800	Epidermolysis bullosa simplex, Weber-Cockayne type		HP:0000006	PMID:7506606	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-12]
OMIM:131800	Epidermolysis bullosa simplex, Weber-Cockayne type		HP:0034193	PMID:17039244	PCS		1/1			P	HPO:probinson[2022-05-12]
OMIM:131800	Epidermolysis bullosa simplex, Weber-Cockayne type		HP:0000962	PMID:9284105	PCS		0/33			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-12]
OMIM:146450	Hypospadias 3, autosomal		HP:0000047	OMIM:146450	IEA					P	HPO:iea[2009-02-17]
OMIM:146450	Hypospadias 3, autosomal		HP:0000006	OMIM:146450	TAS					I	HPO:skoehler[2012-10-17]
OMIM:184705	Steinfeld syndrome		HP:0008718	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0009829	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0000365	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0009927	OMIM:184705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:184705	Steinfeld syndrome		HP:0000480	PMID:8357025	PCS					P	HPO:probinson[2017-12-13]
OMIM:184705	Steinfeld syndrome		HP:0003022	OMIM:184705	TAS				HP:0012832	P	HPO:probinson[2012-05-05]
OMIM:184705	Steinfeld syndrome		HP:0001360	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0000161	OMIM:184705	TAS					P	HPO:probinson[2024-03-29]
OMIM:184705	Steinfeld syndrome		HP:0000193	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0011467	OMIM:184705	TAS					P	HPO:probinson[2012-05-05]
OMIM:184705	Steinfeld syndrome		HP:0000925	OMIM:184705	TAS					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0009099	OMIM:184705	TAS					P	HPO:probinson[2024-03-29]
OMIM:184705	Steinfeld syndrome		HP:0000921	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0000568	OMIM:184705	TAS					P	HPO:probinson[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0000612	PMID:8357025	PCS					P	HPO:probinson[2017-12-13]
OMIM:184705	Steinfeld syndrome		HP:0030680	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0009601	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0001627	OMIM:184705	TAS					P	HPO:skoehler[2015-12-30]
OMIM:184705	Steinfeld syndrome		HP:0000377	OMIM:184705	IEA					P	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0002984	OMIM:184705	TAS				HP:0012832	P	HPO:probinson[2012-05-05]
OMIM:184705	Steinfeld syndrome		HP:0000006	OMIM:184705	IEA					I	HPO:iea[2009-02-17]
OMIM:184705	Steinfeld syndrome		HP:0003468	OMIM:184705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001792	PMID:28343630	PCS		6/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001773	PMID:28343630	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000486	PMID:28343630	PCS		7/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000463	PMID:28343630	PCS		5/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001156	OMIM:617450	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000540	PMID:28343630	PCS		5/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0004322	PMID:28343630	PCS		9/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001252	PMID:28343630	PCS		10/14			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0002020	PMID:28343630	PCS		10/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0002719	PMID:28343630	PCS		5/9			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001629	PMID:28343630	PCS		1/14			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000739	PMID:28343630	PCS		4/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001647	PMID:28343630	PCS		1/14			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000337	PMID:28343630	PCS		8/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0003307	PMID:28343630	PCS		7/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000219	PMID:28343630	PCS		10/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0002019	PMID:28343630	PCS		8/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001249	PMID:28343630	PCS		13/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001601	PMID:28343630	PCS		1/14			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000358	PMID:28343630	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000154	PMID:28343630	PCS		6/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0002136	PMID:28343630	PCS		5/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0002697	PMID:28343630	PCS		1/14			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000750	PMID:28343630	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0002013	PMID:28343630	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0011968	PMID:28343630	PCS		10/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0001263	PMID:28343630	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0025195	PMID:28343630	PCS		1/14			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000729	PMID:28343630	PCS		4/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0010780	PMID:28343630	PCS		7/7			P	HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000722	PMID:28343630	PCS		1/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0200055	PMID:28343630	PCS		10/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0007018	PMID:28343630	PCS		1/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000006	PMID:28343630	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:617450	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold		HP:0000369	PMID:28343630	PCS		7/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:618763	Joubert syndrome 36		HP:0002553	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000486	PMID:30905400	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000463	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000194	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0001250	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0001263	PMID:30905400	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000407	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0011220	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000508	PMID:30905400	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000007	PMID:30905400	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0002419	PMID:30905400	PCS		2/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000768	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0006159	PMID:30905400	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0000256	PMID:30905400	PCS		1/4			P	HPO:probinson[2020-05-11]
OMIM:618763	Joubert syndrome 36		HP:0001249	PMID:30905400	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0012133	PMID:18535205	IEA					P	HPO:probinson[2013-03-12]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0001882	PMID:18535205	IEA					P	HPO:probinson[2013-03-12]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0004322	OMIM:612528	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0001629	PMID:18535205	IEA					P	HPO:probinson[2013-03-12]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0001263	PMID:18535205	IEA					P	HPO:probinson[2013-03-12]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0003593	OMIM:612528	TAS					C	HPO:skoehler[2017-07-13]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0000316	PMID:18535205	IEA					P	HPO:probinson[2013-03-12]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0001896	OMIM:612528	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0001972	PMID:18535205	IEA					P	HPO:probinson[2013-01-09]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0000047	PMID:18535205	IEA					P	HPO:probinson[2013-03-12]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0000369	PMID:18535205	IEA					P	HPO:probinson[2013-03-12]
OMIM:612528	Diamond-Blackfan anemia 5		HP:0000006	OMIM:612528	TAS					I	HPO:skoehler[2017-07-13]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0000121	PMID:16611712	PCS		19/21			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0008619	PMID:16611712	PCS	HP:0011463	9/23			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0002013	PMID:12414817	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0003593	PMID:10973252	PCS		6/9			C	HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0002150	PMID:10973252	PCS		7/9			P	HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0008341	PMID:12414817	PCS		HP:0040280			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0001508	PMID:12414817	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0011463	PMID:10973252	PCS		1/9			C	HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0001944	PMID:12414817	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0002748	PMID:10973252	PCS		2/9			P	HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0000007	PMID:12414817	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-21]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0002900	PMID:10973252;PMID:16611712	PCS		25/27			P	HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0001510	PMID:12414817	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0001942	PMID:12414817	PCS					P	HPO:probinson[2020-09-09]
OMIM:602722	Distal renal tubular acidosis 3, with or without sensorineural hearing loss		HP:0003623	PMID:10973252	PCS		2/9			C	HPO:probinson[2020-09-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0007957	PMID:15037715	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0003236	PMID:15037715;PMID:15637732	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002023	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000485	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001250	PMID:15637732	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001252	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0006829	OMIM:236670	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0012793	PMID:15637732	PCS		1/2			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000518	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000557	OMIM:236670	TAS					P	HPO:skoehler[2012-11-21]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000238	PMID:15637732	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000175	OMIM:236670	TAS					P	HPO:skoehler[2012-11-21]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000252	PMID:15637732	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001344	PMID:15037715	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002079	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000298	PMID:15037715	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000050	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001263	PMID:15037715	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0003560	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001262	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000609	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0007033	OMIM:236670	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000007	OMIM:236670	IEA					I	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000568	PMID:15037715	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000648	PMID:15637732	PCS		1/2			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000204	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000369	PMID:15637732	PCS		1/2			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000340	PMID:15637732	PCS		1/2			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0003577	PMID:15637732	PCS		2/2			C	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000541	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002365	PMID:15037715	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001274	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002085	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0031882	PMID:15637732	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0007260	PMID:12369018;PMID:15037715	PCS		31/31			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000618	OMIM:236670	TAS					P	HPO:skoehler[2012-11-21]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0008551	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001305	PMID:15637732	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0008872	PMID:15637732	PCS		2/2			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002438	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000659	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002119	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001302	OMIM:236670	TAS					P	HPO:skoehler[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000413	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001105	OMIM:236670	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000110	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001321	PMID:15037715	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0007291	OMIM:236670	TAS					P	HPO:skoehler[2012-11-21]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002803	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0001319	PMID:15037715	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0007973	PMID:15637732	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000589	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000501	OMIM:236670	IEA					P	HPO:iea[2009-02-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000545	OMIM:236670	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0002126	OMIM:236670	TAS					P	HPO:skoehler[2012-11-21]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000347	PMID:15637732	PCS		1/2			P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0000028	PMID:15637732	PCS		1/1	MALE		P	HPO:probinson[2021-05-09]
OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		HP:0006888	PMID:15037715	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-09]
OMIM:608569	Cardiomyopathy, dilated, 1O		HP:0003596	PMID:15034580	PCS		3/3			C	HPO:probinson[2022-07-04]
OMIM:608569	Cardiomyopathy, dilated, 1O		HP:0006670	PMID:15034580	PCS		3/3			P	HPO:probinson[2013-03-05]
OMIM:608569	Cardiomyopathy, dilated, 1O		HP:0001635	PMID:15034580	PCS	HP:0003581	3/3			P	HPO:probinson[2022-07-04]
OMIM:608569	Cardiomyopathy, dilated, 1O		HP:0000006	PMID:15034580	PCS					I	HPO:probinson[2013-01-09]
OMIM:608569	Cardiomyopathy, dilated, 1O		HP:0004756	PMID:15034580	PCS		3/3			P	HPO:probinson[2013-03-05]
OMIM:608569	Cardiomyopathy, dilated, 1O		HP:0001644	PMID:15034580	PCS		3/3			P	HPO:probinson[2013-03-05]
OMIM:611038	Microphthalmia, isolated 3		HP:0000528	OMIM:611038	IEA					P	HPO:iea[2009-02-17]
OMIM:611038	Microphthalmia, isolated 3		HP:0000007	OMIM:611038	IEA					I	HPO:iea[2009-02-17]
OMIM:611038	Microphthalmia, isolated 3		HP:0000568	OMIM:611038	IEA					P	HPO:iea[2009-02-17]
OMIM:611038	Microphthalmia, isolated 3		HP:0009755	OMIM:611038	IEA					P	HPO:iea[2009-02-17]
OMIM:611038	Microphthalmia, isolated 3		HP:0000647	OMIM:611038	IEA					P	HPO:iea[2009-02-17]
OMIM:619464	Sick sinus syndrome 4		HP:0011463	PMID:28219978	PCS					C	HPO:probinson[2021-08-20]
OMIM:619464	Sick sinus syndrome 4		HP:0031593	PMID:28219978	PCS		0/11			P	HPO:probinson[2021-08-20]
OMIM:619464	Sick sinus syndrome 4		HP:0033992	PMID:28219978	PCS		2/11			P	HPO:probinson[2021-10-03]
OMIM:619464	Sick sinus syndrome 4		HP:0012723	PMID:28219978	PCS		1/11			P	HPO:probinson[2021-08-20]
OMIM:619464	Sick sinus syndrome 4		HP:0025074	PMID:28219978	PCS		0/11			P	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:619464	Sick sinus syndrome 4		HP:0001279	PMID:28219978	PCS	HP:0011462	3/11			P	HPO:probinson[2021-08-20];HPO:probinson[2021-10-16]
OMIM:619464	Sick sinus syndrome 4		HP:0004757	PMID:28219978	PCS		3/11			P	HPO:probinson[2021-08-20]
OMIM:619464	Sick sinus syndrome 4		HP:0000006	PMID:28219978	PCS					I	HPO:probinson[2021-08-20];HPO:probinson[2021-10-16]
OMIM:619464	Sick sinus syndrome 4		HP:0001678	PMID:28219978	PCS		9/11			P	HPO:probinson[2021-08-20]
OMIM:619464	Sick sinus syndrome 4		HP:0001645	PMID:28219978	PCS		0/11			P	HPO:probinson[2021-08-20];HPO:probinson[2024-03-15]
OMIM:619464	Sick sinus syndrome 4		HP:0001688	PMID:28219978	PCS		5/11			P	HPO:probinson[2021-08-20]
OMIM:619464	Sick sinus syndrome 4		HP:0031547	PMID:28219978	PCS		0/11			P	HPO:probinson[2021-08-20]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0002069	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001276	PMID:33220177	PCS		5/9		HP:0012825	P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0003577	PMID:33220177	PCS		9/9			C	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0002188	PMID:33220177	PCS		2/8			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0002365	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001332	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001274	PMID:33220177	PCS		4/8			P	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001252	PMID:33220177	PCS		6/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0410252	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0032794	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0010862	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0012469	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001903	PMID:33220177	PCS		1/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0000238	PMID:33220177	PCS		1/8			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001522	PMID:33220177	PCS		3/9			C	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001348	PMID:33220177	PCS		8/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0002510	PMID:33220177	PCS		8/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001321	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0002194	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0012434	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0000007	PMID:33220177	PCS					I	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001338	PMID:33220177	PCS		4/8			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0007359	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0001873	PMID:33220177	PCS		2/9		HP:0011010	P	HPO:probinson[2021-05-29]
OMIM:619302	Pontocerebellar hypoplasia, type 15		HP:0009879	PMID:33220177	PCS		6/8			P	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:620583	Optic atrophy 15		HP:0003621	PMID:31915829	PCS		2/2			C	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0000639	PMID:31915829	PCS		2/2			P	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0011462	PMID:33918393	PCS		1/1			C	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0000613	PMID:33918393	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0000007	PMID:31915829	PCS					I	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0007663	PMID:33918393	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0007641	PMID:33918393	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0000648	PMID:31915829;PMID:33918393	PCS		3/3			P	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0000603	PMID:33918393	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0000543	PMID:31915829	PCS		2/2			P	HPO:probinson[2024-03-12]
OMIM:620583	Optic atrophy 15		HP:0002315	PMID:33918393	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:260350	Pancreatic cancer		HP:0002894	OMIM:260350	IEA					P	HPO:skoehler[2013-01-09]
OMIM:260350	Pancreatic cancer		HP:0001442	OMIM:260350	TAS					I	HPO:skoehler[2015-12-30]
OMIM:260350	Pancreatic cancer		HP:0410067	PMID:2311216	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:260350	Pancreatic cancer		HP:0003581	OMIM:260350	TAS					C	HPO:probinson[2022-08-07]
OMIM:260350	Pancreatic cancer		HP:0000006	OMIM:260350	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0002069	PMID:24153177	PCS		2/2			P	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0000582	PMID:24153177	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0002133	PMID:24153177	PCS		1/2			P	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0000463	PMID:24153177	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0001263	PMID:24153177	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0002591	OMIM:615538	TAS					P	HPO:skoehler[2015-07-26]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0100710	PMID:24153177	PCS		1/2			P	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0000418	PMID:24153177	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0000712	PMID:24153177	PCS		1/2			P	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0000736	PMID:24153177	PCS		1/2			P	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0007302	PMID:24153177	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0000537	PMID:24153177	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0003745	PMID:24153177	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-14]
OMIM:615538	Chromosome 22q13 duplication syndrome		HP:0007018	PMID:24153177	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-14]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0010804	PMID:24367057;PMID:30813920	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-28];HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0002521	PMID:24367057	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0000431	PMID:24367057;PMID:30813920	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-28];HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0001344	OMIM:616025	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0000023	PMID:30813920	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0001250	OMIM:616025	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0003155	PMID:24367057	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0001263	OMIM:616025	TAS				HP:0012829	P	HPO:skoehler[2015-01-04]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0003593	PMID:30813920	PCS		1/1			C	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0012736	PMID:24367057	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0000280	PMID:30813920	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0012704	PMID:30813920	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0011344	PMID:30813920	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0032792	PMID:24367057	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0001537	PMID:30813920	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0000007	PMID:24367057	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0000218	PMID:30813920	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0000158	OMIM:616025	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0007359	PMID:30813920	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:616025	Glycosylphosphatidylinositol biosynthesis defect 11		HP:0001249	OMIM:616025	IEA					P	HPO:skoehler[2015-01-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0003037	PMID:24988918;PMID:14740318	PCS		11/14			P	HPO:probinson[2022-04-19];HPO:skoehler[2017-07-13];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002982	OMIM:601559	TAS					P	HPO:probinson[2015-03-01]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001056	PMID:24988918	PCS		5/12			P	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0007759	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002980	PMID:24988918	PCS		6/6			P	HPO:probinson[2015-03-01];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000321	PMID:24988918	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0004322	PMID:24988918	PCS	HP:0003593	2/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0004684	OMIM:601559	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001250	PMID:24988918	PCS		2/12			P	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001252	PMID:24988918	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0003196	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001290	OMIM:601559	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0012745	PMID:24988918	PCS		12/12			P	HPO:probinson[2024-03-10];HPO:skoehler[2014-03-24];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0009185	PMID:24988918	PCS		6/6			P	HPO:probinson[2012-06-04];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0010298	PMID:24988918;PMID:14740318	PCS		13/14			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001609	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0009465	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000954	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001522	PMID:24988918	PCS		3/6			C	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001249	PMID:24988918	PCS		0/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000633	PMID:24988918	PCS		8/12			P	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0007328	PMID:24988918	PCS		6/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0011968	PMID:24988918	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000293	PMID:24988918	PCS		12/12			P	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000490	PMID:24988918	PCS		6/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0011800	PMID:24988918	PCS		4/6			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0004370	PMID:24988918	PCS		6/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001181	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0012810	PMID:24988918	PCS		6/6			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0012385	PMID:24988918	PCS		6/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0006380	OMIM:601559	TAS					P	HPO:probinson[2012-05-27]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000007	PMID:14740318	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000205	PMID:24988918	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001217	PMID:24988918	PCS		3/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002987	OMIM:601559	TAS					P	HPO:probinson[2012-05-27]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0005736	OMIM:601559	TAS					P	HPO:skoehler[2010-06-20]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000883	OMIM:601559	TAS					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002104	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000369	PMID:24988918	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000963	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001611	OMIM:601559	TAS					P	HPO:probinson[2015-03-01]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0004964	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0005019	PMID:24988918;PMID:14740318	PCS		14/14			P	HPO:probinson[2024-02-27]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0003015	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0003577	PMID:24988918	PCS		12/12			C	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0005830	OMIM:601559	TAS					P	HPO:probinson[2015-03-01]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002089	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002486	OMIM:601559	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000463	PMID:24988918	PCS		6/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001156	PMID:24988918	PCS		2/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0004980	PMID:24988918	PCS		6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0008070	PMID:24988918	PCS		12/12			P	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0100865	OMIM:601559	TAS					P	HPO:probinson[2012-06-04]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000939	PMID:24988918	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0012332	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002719	PMID:24988918	PCS		12/12			P	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000935	OMIM:601559	TAS					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000975	PMID:24988918	PCS		5/5			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0009765	PMID:24988918	PCS		6/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001945	PMID:24988918	PCS	HP:0003577	6/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002756	PMID:24988918	PCS		2/6			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0009803	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0003026	OMIM:601559	TAS					P	HPO:probinson[2012-05-27]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001562	PMID:24988918	PCS	HP:0011461	1/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001562	PMID:24988918	PCS		1/6			P	HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002015	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000670	PMID:24988918	PCS		3/3			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002650	PMID:24988918;PMID:14740318	PCS		10/14			P	HPO:probinson[2022-04-19];HPO:probinson[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001883	OMIM:601559	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000233	PMID:24988918	PCS		12/12			P	HPO:probinson[2022-04-19];HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0003300	PMID:24988918	PCS		1/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0005089	OMIM:601559	TAS					P	HPO:probinson[2012-07-29]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000272	OMIM:601559	TAS					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000470	OMIM:601559	TAS					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002092	OMIM:601559	TAS					P	HPO:probinson[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002093	PMID:24988918	PCS		6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0100678	PMID:24988918	PCS		2/6			P	HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0034252	PMID:14740318	PCS		8/8			P	HPO:probinson[2022-06-04]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001954	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0006487	PMID:14740318	PCS	HP:0003577				P	HPO:probinson[2015-03-01];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0007610	OMIM:601559	IEA					P	HPO:iea[2009-02-17]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0002007	PMID:24988918	PCS		2/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0001511	PMID:24988918	PCS		0/6			P	HPO:probinson[2024-03-10]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0008824	OMIM:601559	TAS					P	HPO:probinson[2012-06-04]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0000347	PMID:24988918	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:601559	Stuve-Wiedemann syndrome		HP:0006844	PMID:24988918;OMIM:601559	PCS		8/14			P	HPO:probinson[2022-04-19];HPO:iea[2009-02-17];HPO:probinson[2022-04-19]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0002553	PMID:29534297	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0002059	PMID:29534297	PCS				HP:0003676	P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0002521	PMID:29534297	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0010804	PMID:29534297	PCS		1/4			P	HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0000252	PMID:29534297	PCS		3/4			P	HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0001344	PMID:29534297	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0001272	PMID:29534297	PCS				HP:0003676	P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0001250	PMID:29534297	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0001290	PMID:29534297	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0010851	PMID:29534297	PCS		3/4			P	HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0200134	PMID:29534297	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0002119	PMID:29534297	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0001357	PMID:29534297	PCS		1/4			P	HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0001257	PMID:29534297	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0000006	PMID:29534297	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:618008	Developmental and epileptic encephalopathy 65		HP:0001347	PMID:29534297	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:0008905	OMIM:600121	TAS					P	HPO:probinson[2009-02-17]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:0001508	OMIM:600121	TAS					P	HPO:probinson[2009-02-17]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:0003097	OMIM:600121	TAS				HP:0012828	P	HPO:probinson[2012-07-30]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:0005792	OMIM:600121	TAS				HP:0012828	P	HPO:probinson[2012-07-30]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:0008873	OMIM:600121	TAS					P	HPO:probinson[2009-02-17]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:0000007	PMID:9553082	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-07-05]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:6000427	PMID:9553082	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:600121	Rhizomelic chondrodysplasia punctata, type 3		HP:0010655	OMIM:600121	TAS					P	HPO:probinson[2009-02-17]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000252	PMID:33824500	PCS		8/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0002136	PMID:33824500	PCS		5/12			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0001792	PMID:33824500	PCS		2/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000750	PMID:33824500	PCS		17/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000486	PMID:33824500	PCS		3/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0031936	PMID:33824500	PCS		17/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0001250	PMID:33824500	PCS		7/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0001263	PMID:33824500	PCS		17/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0001252	PMID:33824500	PCS		10/15			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0001285	PMID:33824500	PCS		2/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0030891	PMID:33824500	PCS		1/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0001270	PMID:33824500	PCS		17/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000729	PMID:33824500	PCS		2/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000718	PMID:33824500	PCS		6/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000007	PMID:33824500	PCS					I	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000733	PMID:33824500	PCS		4/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000238	PMID:33824500	PCS		2/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0020045	PMID:33824500	PCS		1/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000648	PMID:33824500	PCS		1/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0000752	PMID:33824500	PCS		2/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0002987	PMID:33824500	PCS		2/17		HP:0012825	P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0001337	PMID:33824500	PCS		5/17			P	HPO:probinson[2021-10-16]
OMIM:619470	Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities		HP:0009879	PMID:33824500	PCS		1/15			P	HPO:probinson[2021-10-16]
OMIM:617475	Specific granule deficiency 2		HP:0033606	PMID:28369036	PCS		4/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0003577	PMID:28369036	PCS					C	HPO:skoehler[2018-10-08];HP:probinson[2018-10-20]
OMIM:617475	Specific granule deficiency 2		HP:0001156	PMID:28369036	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0002164	PMID:28369036	PCS		2/3			P	HPO:skoehler[2018-10-08];HP:probinson[2018-10-20];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0002041	PMID:28369036	PCS		4/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0032434	PMID:28369036	PCS	HP:0003623	4/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0032435	PMID:28369036	PCS	HP:0003623	1/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0012551	PMID:28369036	PCS		4/4			P	HP:probinson[2018-10-20];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0001808	PMID:28369036	PCS		1/3			P	HPO:skoehler[2018-10-08];HP:probinson[2018-10-20]
OMIM:617475	Specific granule deficiency 2		HP:0001508	PMID:28369036	PCS		4/4			P	HP:probinson[2018-10-20]
OMIM:617475	Specific granule deficiency 2		HP:0001903	PMID:28369036	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000938	PMID:28369036	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0002718	PMID:28369036	PCS					P	HP:probinson[2018-10-20]
OMIM:617475	Specific granule deficiency 2		HP:0100806	PMID:28369036	PCS		4/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000956	PMID:28369036	PCS		1/3			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0006532	PMID:28369036	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0001522	PMID:28369036	PCS		1/4			C	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000377	PMID:28369036	PCS		1/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0001007	PMID:28369036	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000974	PMID:28369036	PCS		1/3			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0020206	PMID:28369036	PCS		1/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000358	PMID:28369036	PCS		1/4			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000698	PMID:28369036	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000692	PMID:28369036	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0001263	PMID:28369036	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0003819	PMID:28369036	PCS		1/4			C	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000705	PMID:28369036	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000007	PMID:28369036	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000403	PMID:28369036	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0001852	PMID:28369036	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0001873	PMID:28369036	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0000369	PMID:28369036	PCS		11/14			P	HPO:probinson[2021-09-25];HP:probinson[2018-10-20];HP:probinson[2018-10-20]
OMIM:617475	Specific granule deficiency 2		HP:0002863	PMID:28369036	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-25]
OMIM:617475	Specific granule deficiency 2		HP:0001875	PMID:28369036	PCS		4/4			P	HPO:skoehler[2018-10-08];HP:probinson[2018-10-20]
OMIM:125850	Maturity-onset diabetes of the young, type 1		HP:0031284	OMIM:125850	IEA					P	HPO:skoehler[2018-10-08]
OMIM:125850	Maturity-onset diabetes of the young, type 1		HP:0004904	OMIM:125850	TAS					P	HPO:iea[2009-02-17]
OMIM:125850	Maturity-onset diabetes of the young, type 1		HP:0000006	OMIM:125850	IEA					I	HPO:iea[2009-02-17]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0001696	PMID:24094744	PCS		0/3			P	HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0002110	PMID:24094744;PMID:23991085	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0003593	PMID:23991085	PCS		1/1			C	HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0033036	PMID:24094744;PMID:23991085	PCS		3/3			P	HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0011109	PMID:24094744	PCS		2/3			P	HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0011108	OMIM:615504	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0200073	OMIM:615504	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0012265	PMID:24094744	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0012384	OMIM:615504	TAS				HP:0031796	P	HPO:skoehler[2013-11-18]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0000403	PMID:24094744	PCS		3/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0000007	PMID:24094744	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0002205	PMID:23991085	PCS		1/1			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0002643	PMID:24094744	PCS	HP:0003623	1/3			P	HPO:probinson[2022-03-26]
OMIM:615504	Ciliary dyskinesia, primary, 27		HP:0004469	PMID:24094744	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0025584	OMIM:602078	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0003577	PMID:11600883	PCS					C	HPO:probinson[2022-10-11]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0007936	PMID:11600883	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-11]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0001491	OMIM:602078	IEA					P	HPO:probinson[2009-02-17]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0025586	OMIM:602078	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0000646	OMIM:602078	IEA					P	HPO:probinson[2009-02-17]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0000007	PMID:11600883	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-10-11]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0000505	OMIM:602078	PCS					P	HPO:probinson[2012-04-01]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0001488	PMID:11600883	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-11]
OMIM:602078	Fibrosis of extraocular muscles, congenital, 2		HP:0000577	PMID:11600883	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-11]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0003565	PMID:27633793	PCS		3/3		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0001025	PMID:21360512;PMID:27633793;PMID:18230725	PCS		15/17		HP:0025206;HP:0025206;HP:0025206	P	HPO:probinson[2020-09-26];HPO:probinson[2020-09-26];HPO:probinson[2020-09-26];HPO:skoehler[2014-08-24];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0003593	PMID:18230725	PCS		1/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-26];HPO:probinson[2022-12-03]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0012514	PMID:18230725	PCS		2/3		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0012219	PMID:27633793	PCS		1/3			P	HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0011107	PMID:18230725	PCS				HP:0025206	P	HPO:skoehler[2014-08-24];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0011227	PMID:21360512;PMID:27633793;PMID:18230725	PCS		16/16		HP:0025206;HP:0025206;HP:0025206	P	HPO:probinson[2013-04-02];HPO:probinson[2020-09-26];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0033050	PMID:27633793	PCS		1/3		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0002829	PMID:21360512;PMID:27633793;PMID:18230725	PCS		9/10		HP:0025206;HP:0025206;HP:0025206	P	HPO:probinson[2013-04-02];HPO:probinson[2020-09-26];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0000407	PMID:18230725	PCS		2/3			P	HPO:probinson[2013-04-02];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0003829	OMIM:611762	TAS					I	HPO:skoehler[2018-10-08]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0001954	PMID:18230725	PCS	HP:0003593	3/3		HP:0025206	P	HP:probinson[2018-09-15];HP:probinson[2018-09-15]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0001954	PMID:21360512	PCS		3/4		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0001954	PMID:27633793	PCS		3/3		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0002716	PMID:27633793;PMID:18230725	PCS		3/6		HP:0025206	P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-26];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0000988	OMIM:611762	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0002315	PMID:21360512;PMID:18230725	PCS		5/7		HP:0025206;HP:0025206	P	HPO:probinson[2020-09-26];HPO:skoehler[2014-08-24];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0000006	PMID:18230725	PCS					I	HPO:probinson[2013-01-09]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0002027	PMID:18230725	PCS				HP:0025303	P	HPO:skoehler[2014-08-24];HP:probinson[2018-09-15]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0001744	PMID:27633793	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0003326	PMID:21360512;PMID:18230725	PCS		5/7		HP:0025206;HP:0025206	P	HPO:probinson[2013-04-02];HPO:probinson[2020-09-26];HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0001369	OMIM:611762	TAS					P	HPO:skoehler[2018-10-08]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0001974	PMID:27633793	PCS		3/3		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:611762	Familial cold autoinflammatory syndrome 2		HP:0003623	PMID:18230725	PCS		2/3			C	HPO:probinson[2022-12-03]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000286	PMID:16551969	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0003577	PMID:16537806	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000582	OMIM:608233	TAS					P	HPO:iea[2009-02-17]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000343	PMID:16551969	PCS		1/1			P	HPO:probinson[2012-05-01];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000486	OMIM:608233	PCS					P	HPO:iea[2009-02-17]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0008807	PMID:16551969	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0002286	PMID:11809908	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0002020	PMID:11809908	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0002240	PMID:11809908	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0003010	PMID:16551969	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000280	PMID:16551969	PCS	HP:0003577	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000280	PMID:16537806	PCS		2/2			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001270	PMID:11809908	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0012177	PMID:16551969	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000639	PMID:16551969	PCS	HP:0003577	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000639	PMID:16537806	PCS		2/2			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0007384	PMID:16537806	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0011342	PMID:16537806	PCS		2/2			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000319	OMIM:608233	TAS					P	HPO:probinson[2012-05-01]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0002718	PMID:11809908	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000613	PMID:16537806	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001107	PMID:16537806	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0007663	PMID:16537806	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000219	PMID:11809908	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0006532	PMID:16537806	PCS		1/2			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000358	PMID:16551969;PMID:11809908	PCS		2/2			P	HPO:probinson[2020-11-02];HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001744	PMID:16537806;PMID:11809908	PCS		3/3			P	HPO:probinson[2020-11-02];HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0040218	PMID:16537806	PCS		2/2			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001022	PMID:16551969	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000670	PMID:16537806	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000252	PMID:8042664	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000431	PMID:16551969;PMID:11809908	PCS		2/2			P	HPO:probinson[2020-11-02];HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0009098	PMID:16551969	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0033264	PMID:402573	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0033263	PMID:11809908	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000704	PMID:16537806	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0033222	PMID:11809908	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000007	PMID:10024875	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000403	PMID:16551969	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0002722	PMID:16537806	PCS		1/2			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0007513	PMID:16537806	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001433	PMID:16551969	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0002206	OMIM:608233	IEA					P	HPO:iea[2009-02-17]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001873	PMID:16537806	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000666	PMID:11809908	PCS	HP:0003577	1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0004866	PMID:16551969	PCS		1/1			P	HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0000369	PMID:16551969;PMID:11809908	PCS		2/2			P	HPO:probinson[2020-11-02];HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001875	PMID:16551969	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-02]
OMIM:608233	Hermansky-Pudlak syndrome 2		HP:0001875	PMID:16537806	PCS	HP:0003577	2/2			P	HPO:probinson[2020-11-02]
OMIM:265200	Pulmonary bullae causing pneumothorax		HP:0000007	OMIM:265200	IEA					I	HPO:iea[2009-02-17]
OMIM:265200	Pulmonary bullae causing pneumothorax		HP:0006522	OMIM:265200	IEA					P	HPO:iea[2009-02-17]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000044	PMID:17761593	PCS					P	HPO:probinson[2017-05-29];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000054	OMIM:228300	TAS					P	HPO:skoehler[2015-04-19]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000771	PMID:17761593;PMID:15602022	PCS		2/3			P	HPO:probinson[2022-03-13];HPO:skoehler[2015-04-19];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0030344	PMID:17761593;PMID:15602022	PCS		3/3			P	HPO:probinson[2017-05-29];HPO:probinson[2022-03-13];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0040171	PMID:17761593;PMID:1727547;PMID:15602022	PCS		4/4			P	HPO:probinson[2017-05-29];HPO:probinson[2022-03-13];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0010789	PMID:17761593	PCS					P	HPO:probinson[2017-05-29];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0033810	PMID:15602022	PCS		1/1			P	HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0012215	OMIM:228300	TAS					P	HPO:skoehler[2015-04-19]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0025708	PMID:1727547;PMID:15602022	PCS		2/2			C	HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000869	OMIM:228300	TAS					P	HPO:skoehler[2015-04-19]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0008232	PMID:17761593;PMID:15602022	PCS		3/3			P	HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000007	PMID:1727547	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000876	OMIM:228300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0004408	PMID:17761593	PCS		0/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0008226	OMIM:228300	IEA					P	HPO:iea[2009-02-17]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000823	PMID:1727547	PCS					P	HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000026	PMID:17761593	PCS		2/2			P	HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000138	OMIM:228300	TAS					P	HPO:probinson[2017-05-29]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0002225	PMID:15602022	PCS		1/1			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0008669	PMID:17761593	PCS					P	HPO:probinson[2017-05-29];HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0000027	PMID:17761593;PMID:15602022	PCS		3/3			P	HPO:probinson[2022-03-13]
OMIM:228300	Hypogonadotropic hypogonadism 23 without anosmia		HP:0002215	PMID:17761593	PCS		1/1			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-03-13]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002521	PMID:15385443	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002188	PMID:15385443	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002023	OMIM:613161	IEA					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002167	OMIM:613161	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001332	PMID:15385443	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001250	PMID:15385443	PCS		1/4			P	HPO:skoehler[2012-07-25];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:6000696	PMID:15385443	PCS		4/4			P	HPO:probinson[2024-05-09]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001252	PMID:15385443	PCS		1/4			P	HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:6000210	OMIM:613161	TAS					P	HPO:probinson[2024-02-09]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0003593	PMID:15385443	PCS		4/4			C	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001270	PMID:15385443	PCS		1/4			P	HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:6000534	PMID:11675655	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0007185	PMID:15385443	PCS		1/4			P	HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002836	OMIM:613161	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001942	PMID:15385443	PCS		1/4			P	HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001249	PMID:15385443	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:6000082	PMID:35151535	PCS		4/4			P	HPO:probinson[2024-01-06];HPO:probinson[2024-01-06]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0000252	OMIM:613161	TAS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002133	PMID:15385443	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002650	PMID:15385443	PCS		1/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0002151	PMID:15385443	PCS		1/4			P	HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001263	PMID:15385443	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:6000623	PMID:12271438	PCS					P	HPO:probinson[2024-04-03]
OMIM:613161	Beta-ureidopropionase deficiency		HP:6000622	PMID:12271438	PCS					P	HPO:probinson[2024-04-03]
OMIM:613161	Beta-ureidopropionase deficiency		HP:6000209	OMIM:613161	TAS					P	HPO:probinson[2024-02-09]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0034595	OMIM:613161	TAS					P	HPO:probinson[2023-03-31]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0000007	PMID:15385443	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-28]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0001319	OMIM:613161	TAS					P	HPO:skoehler[2010-06-19]
OMIM:613161	Beta-ureidopropionase deficiency		HP:0000048	OMIM:613161	IEA					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-28]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0003577	PMID:24035193	PCS		13/13			C	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000365	PMID:24035193;PMID:29593478	PCS		4/12			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001278	PMID:24035193	PCS		3/11			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000486	PMID:24035193	PCS		3/11			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0009916	PMID:24035193	PCS		3/11			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0003474	PMID:24035193	PCS		2/12			P	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001252	PMID:24035193;PMID:29593478	PCS		5/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001251	PMID:24035193	PCS		1/10			P	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0003593	PMID:24035193	PCS		13/13			C	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001290	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000639	PMID:24035193	PCS		2/11			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0010450	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0002714	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0020049	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001249	PMID:24035193;PMID:29593478	PCS		12/13			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001347	PMID:24035193	PCS		2/12			P	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0003623	PMID:29593478	PCS		2/2			C	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0002015	PMID:24035193	PCS		3/13			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000750	PMID:24035193;PMID:29593478	PCS		11/11			P	HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0002571	PMID:24035193;PMID:29593478	PCS		13/14			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0011968	PMID:24035193;PMID:29593478	PCS		4/15			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001263	PMID:24035193;PMID:29593478	PCS		15/15			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0009890	PMID:29593478	PCS		1/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000508	PMID:24035193	PCS		1/8			P	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000448	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000007	PMID:24035193	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000846	PMID:24035193	PCS		0/13			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000966	PMID:24035193	PCS		3/11			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000322	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001257	PMID:24035193	PCS		2/10			P	HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000666	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0002643	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000325	PMID:29593478	PCS		2/2			P	HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000522	PMID:24035193;PMID:29593478	PCS		15/15			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0000962	PMID:24035193	PCS		3/11			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05]
OMIM:615510	Alacrima, achalasia, and impaired intellectual development syndrome		HP:0001611	PMID:24035193;PMID:29593478	PCS		4/12			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-05];HP:probinson[2022-03-05]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0004322	PMID:28972538	IEA		2/3			P	HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0033607	PMID:28972538	PCS		3/3			P	HPO:probinson[2024-03-16]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0001263	PMID:28972538	PCS					P	HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0002570	PMID:28972538	PCS		1/3			P	HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0010701	PMID:28972538	PCS		0/2			P	HPO:probinson[2020-04-06];HPO:probinson[2024-03-16]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0001738	PMID:28972538	PCS		2/3			P	HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0011463	PMID:28972538	PCS		1/3			C	HPO:probinson[2024-03-16]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0000729	PMID:28972538	PCS		2/2			P	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0008872	PMID:28972538	PCS	HP:0003593	2/3			P	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0002910	PMID:28972538	PCS		1/3			P	HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0000006	PMID:28972538	PCS					I	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0001875	PMID:28972538	PCS	HP:0003577	3/3			P	HPO:probinson[2020-04-06]
OMIM:618752	Neutropenia, severe congenital, 8, autosomal dominant		HP:0003623	PMID:28972538	PCS		2/3			C	HPO:probinson[2024-03-16]
OMIM:609887	Glaucoma 1, open angle, G		HP:0012108	OMIM:609887	TAS					P	HPO:probinson[2013-01-09]
OMIM:300498	Intellectual developmental disorder, X-linked 45		HP:0004322	OMIM:300498	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300498	Intellectual developmental disorder, X-linked 45		HP:0001419	PMID:15121780	TAS					I	HPO:probinson[2013-01-09]
OMIM:300498	Intellectual developmental disorder, X-linked 45		HP:0000426	OMIM:300498	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300498	Intellectual developmental disorder, X-linked 45		HP:0000218	OMIM:300498	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300498	Intellectual developmental disorder, X-linked 45		HP:0000400	PMID:15121780	TAS					P	HPO:probinson[2013-02-17]
OMIM:300498	Intellectual developmental disorder, X-linked 45		HP:0000411	OMIM:300498	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300498	Intellectual developmental disorder, X-linked 45		HP:0001249	PMID:15121780	TAS					P	HPO:probinson[2013-02-17]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0003026	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0009826	PMID:29122926	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0007957	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0003016	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0005787	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0001156	PMID:29122926	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0000463	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0003177	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0003196	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0030320	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0004592	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0100670	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0011344	PMID:29122926	PCS					P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0005280	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0003819	PMID:29122926	PCS		1/2			C	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0000316	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0000007	PMID:29122926	PCS					I	HPO:probinson[2020-08-27];HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0001319	PMID:29122926	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0000774	PMID:29122926	IEA	HP:0003577	2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0001643	PMID:29122926	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0000773	PMID:29122926	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0000520	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0002643	PMID:29122926	PCS	HP:0003577	2/2			P	HPO:probinson[2020-08-27]
OMIM:618961	Spondylometaphyseal dysplasia with corneal dystrophy		HP:0004568	PMID:29122926	PCS		2/2			P	HPO:probinson[2020-08-27]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0001561	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0003200	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0003542	OMIM:616794	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0001263	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0004396	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0002151	OMIM:616794	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0003593	PMID:26522469	PCS					C	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0001290	OMIM:616794	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0011923	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0012378	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0003828	OMIM:616794	TAS					M	HPO:skoehler[2017-07-13]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0000007	PMID:26522469	PCS					I	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0001558	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0001635	OMIM:616794	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0002878	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0008347	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0001324	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0004900	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:616794	Combined oxidative phosphorylation deficiency 28		HP:0002027	PMID:26522469	PCS					P	HPO:probinson[2017-06-18]
OMIM:607841	Deafness, autosomal dominant 48		HP:0000407	PMID:12736868	IEA					P	HPO:probinson[2013-03-04]
OMIM:607841	Deafness, autosomal dominant 48		HP:0000006	PMID:12736868	IEA					I	HPO:probinson[2013-01-09]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0003577	PMID:20734336	PCS		5/5			C	HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0005113	PMID:20734336	PCS		2/5			P	HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0012727	PMID:20734336	PCS		5/5			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0030891	OMIM:613834	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0034324	PMID:20734336	PCS		2/5			P	HPO:probinson[2022-09-05]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0032398	PMID:34857515	PCS		12/13			P	HPO:probinson[2024-02-11]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0011499	PMID:20734336	PCS	HP:0003577	5/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0002092	OMIM:613834	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0034325	PMID:20734336	PCS		2/5			P	HPO:probinson[2022-09-05]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0100771	PMID:20734336	PCS		2/5			P	HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0031252	PMID:20734336	PCS		1/5			P	HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0000822	OMIM:613834	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0004927	PMID:20734336	PCS		3/5			P	HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0002617	PMID:20734336	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0001643	PMID:20734336	PCS		5/5			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0001631	PMID:20734336	PCS		1/5			P	HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0004944	OMIM:613834	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0002789	PMID:20734336	PCS	HP:0003623	4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0000006	PMID:20734336	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0000028	PMID:20734336	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0002566	PMID:20734336	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:613834	Multisystemic smooth muscle dysfunction syndrome		HP:0007866	OMIM:613834	TAS					P	HPO:skoehler[2012-11-21]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002025	PMID:8444246	PCS		1/108			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0003016	PMID:10494084	PCS					P	HPO:probinson[2015-03-07]
OMIM:250250	Cartilage-hair hypoplasia		HP:0003577	PMID:8444246	PCS		32/42			C	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002980	OMIM:250250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001377	PMID:8444246	PCS		79/86			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0003311	OMIM:250250	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002024	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002286	PMID:8444246	PCS		81/87			P	HPO:probinson[2012-03-01];HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0005374	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0003593	PMID:8444246	PCS		9/42			C	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0100255	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0045075	OMIM:250250	TAS					P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0008070	OMIM:250250	TAS		81/87			P	HPO:probinson[2012-03-01];HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002719	PMID:8444246	PCS		58/103			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0008450	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0011463	PMID:8444246	PCS		1/42			C	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001903	PMID:8444246	PCS	HP:0011463	67/85			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002938	PMID:8444246	PCS		72/85			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0007464	OMIM:250250	TAS					P	HPO:probinson[2012-03-01]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001888	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002812	PMID:8444246	PCS		54/86			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0000653	OMIM:250250	TAS					P	HPO:probinson[2012-03-01]
OMIM:250250	Cartilage-hair hypoplasia		HP:0000774	PMID:8444246	PCS		34/84			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002019	PMID:8444246	PCS		5/108			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0003347	OMIM:250250	PCS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001623	PMID:8444246	PCS		17/81			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0004810	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002213	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002650	PMID:8444246	PCS		18/86		HP:0012825	P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0004279	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002032	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001382	PMID:8444246;OMIM:250250	PCS		91/95			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002671	PMID:8444246	PCS		3/103			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002251	PMID:8444246	PCS		8/108			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0003021	PMID:10494084	PCS					P	HPO:probinson[2015-03-07]
OMIM:250250	Cartilage-hair hypoplasia		HP:0005360	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0031087	OMIM:250250	IEA					P	HPO:skoehler[2018-10-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0000007	OMIM:250250	TAS					I	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0008921	OMIM:250250	IEA					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0000884	PMID:8444246	PCS		28/84			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001555	PMID:8444246	PCS		5/84			P	HPO:probinson[2022-05-08]
OMIM:250250	Cartilage-hair hypoplasia		HP:0006589	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001972	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0000248	OMIM:250250	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002665	PMID:11124791	PCS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0002644	OMIM:250250	IEA					P	HPO:probinson[2009-02-17]
OMIM:250250	Cartilage-hair hypoplasia		HP:0001875	OMIM:250250	TAS					P	HPO:probinson[2009-02-17]
OMIM:602087	Arrhythmogenic right ventricular dysplasia, familial, 4		HP:0003140	OMIM:602087	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602087	Arrhythmogenic right ventricular dysplasia, familial, 4		HP:0004308	OMIM:602087	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602087	Arrhythmogenic right ventricular dysplasia, familial, 4		HP:0011663	OMIM:602087	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602087	Arrhythmogenic right ventricular dysplasia, familial, 4		HP:0003338	OMIM:602087	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602087	Arrhythmogenic right ventricular dysplasia, familial, 4		HP:0000006	OMIM:602087	TAS					I	HPO:skoehler[2009-02-17]
OMIM:602087	Arrhythmogenic right ventricular dysplasia, familial, 4		HP:0001699	OMIM:602087	TAS					P	HPO:skoehler[2009-02-17]
OMIM:620540	Developmental delay with or without epilepsy		HP:0002069	PMID:36331550;PMID:29050398	PCS		1/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0003577	PMID:36331550	PCS		1/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0000486	PMID:36331550	PCS		3/16			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0002384	PMID:36331550;PMID:29050398	PCS		1/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0001272	PMID:36331550;PMID:29050398	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0001250	PMID:36331550	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0002121	PMID:36331550;PMID:29050398	PCS		2/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0001252	PMID:36331550;PMID:29050398	PCS		3/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0001251	PMID:36331550;PMID:29050398	PCS		5/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0002064	PMID:29050398	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0003593	PMID:36331550	PCS		5/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0032794	PMID:36331550;PMID:29050398	PCS		4/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0010841	PMID:36331550;PMID:29050398	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0001270	PMID:36331550	PCS		10/16			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0012469	PMID:36331550;PMID:29050398	PCS		1/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0000639	PMID:36331550	PCS		2/16			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0007340	PMID:36331550	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0011463	PMID:36331550;PMID:29050398	PCS		12/18			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0006895	PMID:36331550;PMID:29050398	PCS		1/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0001249	PMID:36331550;PMID:29050398	PCS		15/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0000252	PMID:36331550;PMID:29050398	PCS		4/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0000750	PMID:36331550	PCS		13/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0002373	PMID:36331550;PMID:29050398	PCS		4/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0002395	PMID:36331550;PMID:29050398	PCS		1/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0010819	PMID:36331550;PMID:29050398	PCS		1/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0002392	PMID:36331550;PMID:29050398	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0012015	PMID:36331550;PMID:29050398	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0000729	PMID:29050398	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0007018	PMID:36331550;PMID:29050398	PCS		3/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0001257	PMID:36331550	PCS		0/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0007359	PMID:29050398	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620540	Developmental delay with or without epilepsy		HP:0000006	PMID:36331550	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0002166	OMIM:611945	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0000012	OMIM:611945	TAS					P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0003487	OMIM:611945	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0002395	OMIM:611945	TAS					P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0000020	OMIM:611945	TAS					P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0002064	OMIM:611945	TAS					P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0002061	OMIM:611945	TAS					P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0011448	OMIM:611945	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0007350	OMIM:611945	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0001258	OMIM:611945	IEA					P	HPO:skoehler[2015-01-27]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0000006	OMIM:611945	TAS					I	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0006986	OMIM:611945	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:611945	Spastic paraplegia 37, autosomal dominant		HP:0003677	OMIM:611945	TAS					C	HPO:skoehler[2012-10-17]
OMIM:602093	Cone dystrophy 3		HP:0000529	OMIM:602093	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602093	Cone dystrophy 3		HP:0000613	OMIM:602093	IEA					P	HPO:iea[2009-02-17]
OMIM:602093	Cone dystrophy 3		HP:0007663	OMIM:602093	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602093	Cone dystrophy 3		HP:0000548	OMIM:602093	TAS					P	HPO:skoehler[2015-07-26]
OMIM:602093	Cone dystrophy 3		HP:0007401	OMIM:602093	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:602093	Cone dystrophy 3		HP:0000006	OMIM:602093	IEA					I	HPO:iea[2009-02-17]
OMIM:613820	Nephronophthisis 12		HP:0003774	PMID:21258341	PCS					P	HPO:probinson[2013-08-10]
OMIM:613820	Nephronophthisis 12		HP:0000007	PMID:21258341	PCS					I	HPO:probinson[2013-08-10]
OMIM:613820	Nephronophthisis 12		HP:0000090	PMID:21258341	PCS					P	HPO:probinson[2013-08-10]
OMIM:613820	Nephronophthisis 12		HP:0000006	OMIM:613820	TAS					I	HPO:skoehler[2017-07-13]
OMIM:606593	LIG4 syndrome		HP:0000286	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000341	PMID:16088910	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:606593	LIG4 syndrome		HP:0000483	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000582	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000141	OMIM:606593	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606593	LIG4 syndrome		HP:0033005	PMID:11779494	PCS		1/4			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0001508	OMIM:606593	IEA					P	HPO:skoehler[2019-09-07]
OMIM:606593	LIG4 syndrome		HP:0001009	PMID:11779494	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0003765	PMID:11779494	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000252	PMID:16088910;PMID:11779494	PCS		5/5			P	HPO:probinson[2023-04-08];HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000054	PMID:16088910	PCS		1/1	MALE		P	HPO:skoehler[2019-04-18]
OMIM:606593	LIG4 syndrome		HP:0000992	PMID:11779494	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000750	OMIM:606593	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606593	LIG4 syndrome		HP:0000431	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0002099	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0001263	PMID:16088910	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:606593	LIG4 syndrome		HP:0000294	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0011109	PMID:11779494	PCS		1/4			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0001518	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000448	PMID:16088910	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000007	PMID:11779494	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000601	OMIM:606593	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606593	LIG4 syndrome		HP:0000821	PMID:11779494	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0004209	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0002205	PMID:11779494	PCS		1/4			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0006721	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0001873	PMID:11779494	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0005978	PMID:11779494	PCS		1/4			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000248	PMID:16088910	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:606593	LIG4 syndrome		HP:0000028	PMID:16088910	PCS		1/1	MALE		P	HPO:skoehler[2019-04-18]
OMIM:606593	LIG4 syndrome		HP:0002863	OMIM:606593	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606593	LIG4 syndrome		HP:0001876	PMID:11779494	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000341	PMID:26733463	PCS		1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0010804	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000343	PMID:26733463	PCS		1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0002089	PMID:26733463	PCS	HP:0030674	2/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0002089	PMID:30403323	PCS		0/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001531	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000089	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0003198	PMID:31260566;PMID:30403323	PCS		2/2			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001290	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0012801	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001270	PMID:31260566;PMID:30403323	PCS		2/2			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000319	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001845	PMID:26733463	PCS	HP:0003577	2/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001989	PMID:26733463	PCS	HP:0030674				P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000218	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0030084	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000774	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000476	PMID:26733463	PCS	HP:0030674	2/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001188	PMID:26733463	PCS		1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000494	PMID:26733463	PCS	HP:0003577	1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000494	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000494	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001561	PMID:26733463	PCS	HP:0030674	2/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001561	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000175	PMID:26733463	PCS	HP:0030674	3/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000331	PMID:26733463	PCS	HP:0030674	2/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0011947	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0005684	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000074	PMID:26733463	PCS	HP:0003577	1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0001182	PMID:26733463	PCS	HP:0003577	1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0002093	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0010557	PMID:26733463	PCS	HP:0030674	1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0010557	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0009110	PMID:26733463	PCS	HP:0030674	1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000506	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0009891	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000508	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000767	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000007	PMID:26733463	PCS					I	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000348	PMID:26733463	PCS		1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000689	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000565	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000520	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000303	PMID:30403323	PCS		1/1			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000325	PMID:31260566;PMID:30403323	PCS		2/2			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000369	PMID:31260566	PCS		1/1			P	HPO:probinson[2020-09-12]
OMIM:618975	Myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies		HP:0000126	PMID:26733463	PCS	HP:0030674	1/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0002751	PMID:12552556	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0003577	PMID:12552556	PCS		9/9			C	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0003236	PMID:12552556	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0001371	PMID:12552556	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0001250	PMID:12552556	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0001252	PMID:12552556	PCS	HP:0003577	9/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0001284	OMIM:607855	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0003560	PMID:12552556	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0001270	PMID:12552556	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0100297	OMIM:607855	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0000602	OMIM:607855	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0000007	PMID:7550355	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0008872	OMIM:607855	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0007103	OMIM:607855	IEA					P	HPO:iea[2009-02-17]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0002747	OMIM:607855	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0001324	PMID:12552556	PCS		9/9			P	HPO:probinson[2021-02-21]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0002536	OMIM:607855	IEA					P	HPO:iea[2009-02-17]
OMIM:607855	Muscular dystrophy, congenital, merosin deficient or partially deficient		HP:0001249	OMIM:607855	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:616780	Oocyte maturation defect 2		HP:0031516	PMID:26789871;OMIM:616780	PCS		20/20			P	HPO:lccarmody[2018-10-03];HPO:skoehler[2018-10-08]
OMIM:616780	Oocyte maturation defect 2		HP:0008222	PMID:27273344	PCS					P	HPO:probinson[2017-06-18]
OMIM:616780	Oocyte maturation defect 2		HP:0000007	OMIM:616780	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616780	Oocyte maturation defect 2		HP:0000006	OMIM:616780	TAS					I	HPO:skoehler[2017-07-13]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0006380	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0011463	PMID:35789258	PCS		1/1			C	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0030431	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0003273	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0012191	PMID:35789258	PCS	HP:0025708	1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0000007	PMID:35789258	PCS					I	HPO:probinson[2024-08-03]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0006466	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0008445	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0008940	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0002953	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0004349	PMID:35789258	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620232	Joint contracture, osteochondromas, and B-cell lymphoma		HP:0030080	PMID:35789258	PCS	HP:0025709	1/1			P	HPO:probinson[2023-06-16]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0031417	PMID:23255504	PCS		31/34		HP:0011010	P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0001696	PMID:21131974	PCS	HP:0003577	11/16			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0002110	PMID:23255504	PCS		17/33			P	HPO:probinson[2013-08-10];HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0012735	PMID:23255504	PCS		35/35		HP:0011010	P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0030828	PMID:23255504	PCS		35/35		HP:0011010	P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0100582	PMID:23255504	PCS		4/34			P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0012208	PMID:23255504	PCS		2/2			P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0011109	PMID:23255504	PCS		31/34			P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0012258	PMID:23255504	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0012265	PMID:23255504	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0000789	PMID:23255504	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0000007	PMID:21131974	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0000403	PMID:23255504	PCS		31/35			P	HPO:probinson[2013-08-10];HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0006532	PMID:23255504	PCS		20/32			P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0002205	PMID:23255504	PCS		34/36			P	HPO:probinson[2013-08-10];HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0002643	PMID:23255504	PCS		25/35			P	HPO:probinson[2021-05-09]
OMIM:613808	Ciliary dyskinesia, primary, 15		HP:0004469	PMID:23255504	PCS		35/35			P	HPO:probinson[2021-05-09]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0001265	PMID:29127354	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0033748	PMID:30489379	PCS		1/1			P	HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0030237	PMID:30489379	PCS		1/1			P	HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0003621	PMID:30489379	PCS		1/1			C	HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0003431	PMID:30489379;PMID:29127354	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0003481	OMIM:162500	IEA					P	HPO:iea[2009-02-17]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0033660	PMID:30489379	PCS		1/1			P	HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0011462	PMID:29127354	PCS		1/1			C	HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0032121	PMID:30489379	PCS		1/1			P	HPO:probinson[2022-04-03]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0009830	OMIM:162500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0001605	OMIM:162500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0001324	OMIM:162500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162500	Neuropathy, hereditary, with liability to pressure palsies		HP:0000006	PMID:8422677	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:306980	Hirschsprung disease with type D brachydactyly		HP:0002251	OMIM:306980	IEA					P	HPO:iea[2009-02-17]
OMIM:306980	Hirschsprung disease with type D brachydactyly		HP:0005627	OMIM:306980	IEA					P	HPO:iea[2009-02-17]
OMIM:306980	Hirschsprung disease with type D brachydactyly		HP:0009778	OMIM:306980	TAS					P	HPO:skoehler[2009-02-17]
OMIM:166000	Enchondromatosis, multiple		HP:0011314	OMIM:166000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:166000	Enchondromatosis, multiple		HP:0006765	OMIM:166000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:166000	Enchondromatosis, multiple		HP:0000006	OMIM:166000	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:166000	Enchondromatosis, multiple		HP:0001028	OMIM:166000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:166000	Enchondromatosis, multiple		HP:0005701	OMIM:166000	TAS					P	HPO:skoehler[2013-04-01]
OMIM:614815	Joubert syndrome 18		HP:0003577	PMID:22883145	PCS		2/8			C	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0002085	PMID:22883145	PCS		6/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0001274	PMID:22883145	PCS		1/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0000085	PMID:22883145	PCS		1/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0000180	PMID:22883145	PCS		1/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0001629	PMID:22883145	PCS		1/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0034044	PMID:22883145	PCS		3/5			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0002419	PMID:22883145	PCS		4/8			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0002139	PMID:22883145	PCS		1/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0000278	PMID:22883145	PCS		2/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0001249	PMID:22883145	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0002335	PMID:22883145	PCS		2/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0002751	PMID:22883145	PCS		1/8		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0005248	PMID:22883145	PCS		6/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0000175	PMID:22883145	PCS		1/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0001762	PMID:22883145	PCS		1/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0000496	PMID:22883145	PCS		1/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0001382	PMID:22883145	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0012385	PMID:22883145	PCS		1/8			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0100259	PMID:22883145	PCS		7/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0034198	PMID:22883145	PCS		6/8			C	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0000107	PMID:22883145	PCS		6/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0000007	PMID:22883145	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0006487	PMID:22883145	PCS		2/8			P	HPO:probinson[2022-11-26]
OMIM:614815	Joubert syndrome 18		HP:0001511	PMID:22883145	PCS		3/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:218200	Cranial nerves, recurrent paresis of		HP:0000819	OMIM:218200	IEA					P	HPO:iea[2009-02-17]
OMIM:218200	Cranial nerves, recurrent paresis of		HP:0010628	OMIM:218200	IEA					P	HPO:iea[2009-02-17]
OMIM:218200	Cranial nerves, recurrent paresis of		HP:0007250	OMIM:218200	IEA					P	HPO:iea[2009-02-17]
OMIM:218200	Cranial nerves, recurrent paresis of		HP:0009830	OMIM:218200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:218200	Cranial nerves, recurrent paresis of		HP:0000007	OMIM:218200	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:255300	Myopathy, congenital		HP:0003198	OMIM:255300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255300	Myopathy, congenital		HP:0000707	OMIM:255300	IEA					P	HPO:iea[2009-02-17]
OMIM:255300	Myopathy, congenital		HP:0000007	OMIM:255300	IEA					I	HPO:iea[2009-02-17]
OMIM:580000	Deafness, aminoglycoside-induced		HP:0011975	PMID:16152638	PCS					P	HPO:probinson[2012-07-18];HPO:probinson[2022-05-15]
OMIM:580000	Deafness, aminoglycoside-induced		HP:0001427	PMID:16152638	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-15]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0003577	PMID:35470444;PMID:29379197	PCS		4/16			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000486	PMID:35470444	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000343	PMID:35470444;PMID:29379197	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000463	PMID:35470444	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000023	PMID:29379197	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0003196	PMID:35470444;PMID:29379197	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0002020	PMID:29379197	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0003593	PMID:35470444	PCS		10/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0410030	PMID:29379197	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0045075	PMID:35470444	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0001629	PMID:35470444;PMID:29379197	PCS		3/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0010034	PMID:29379197	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000913	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000316	PMID:29379197	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0006695	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0004935	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000675	PMID:35470444	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0200021	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0001249	PMID:35470444;PMID:29379197	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0002236	PMID:35470444	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000358	PMID:29379197	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0002553	PMID:35470444;PMID:29379197	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0001166	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000252	PMID:35470444;PMID:29379197	PCS		15/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000494	PMID:35470444	PCS		3/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0001385	PMID:35470444;PMID:29379197	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0002650	PMID:35470444	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0004279	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000750	PMID:29379197	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0002079	PMID:35470444	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0002750	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0001263	PMID:35470444;PMID:29379197	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000709	PMID:35470444	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0012167	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0034197	PMID:35470444	PCS		1/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000506	PMID:29379197	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0034198	PMID:35470444	PCS		1/14			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000722	PMID:35470444	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0004209	PMID:35470444	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000768	PMID:35470444	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0001511	PMID:35470444;PMID:29379197	PCS		5/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000400	PMID:35470444	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000664	PMID:35470444;PMID:29379197	PCS		8/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000369	PMID:35470444	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620568	Cornelia de Lange syndrome 6		HP:0000006	PMID:29379197	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:251600	Microphthalmia, isolated 1		HP:0000528	OMIM:251600	TAS					P	HPO:probinson[2009-02-17]
OMIM:251600	Microphthalmia, isolated 1		HP:0008499	OMIM:251600	TAS					P	HPO:probinson[2009-02-17]
OMIM:251600	Microphthalmia, isolated 1		HP:0000007	OMIM:251600	IEA					I	HPO:iea[2009-02-17]
OMIM:251600	Microphthalmia, isolated 1		HP:0000568	OMIM:251600	IEA					P	HPO:iea[2009-02-17]
OMIM:251600	Microphthalmia, isolated 1		HP:0000501	OMIM:251600	IEA					P	HPO:iea[2009-02-17]
OMIM:614424	Joubert syndrome 14		HP:0000286	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0010804	OMIM:614424	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614424	Joubert syndrome 14		HP:0000486	PMID:22152675	PCS		9/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0002365	PMID:22152675	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0001252	OMIM:614424	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614424	Joubert syndrome 14		HP:0001251	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0001290	OMIM:614424	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614424	Joubert syndrome 14		HP:0002084	PMID:22152675	PCS		7/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000639	PMID:22152675	PCS		12/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0001629	PMID:22152675	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000737	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0100704	PMID:22152675	PCS		2/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000316	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0001305	PMID:22152675	PCS		4/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000238	PMID:22152675	PCS		10/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0002419	PMID:22152675	PCS		9/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0025514	PMID:22152675	PCS		3/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000358	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0002335	PMID:22152675	PCS		3/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0002435	PMID:22152675	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0002553	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0001320	PMID:22152675	PCS		2/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000494	OMIM:614424	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614424	Joubert syndrome 14		HP:0000175	PMID:22152675	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0002079	PMID:22152675	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000194	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0000490	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0001263	OMIM:614424	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614424	Joubert syndrome 14		HP:0000272	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0002170	PMID:22152675	PCS		1/19			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0100259	PMID:22152675	PCS		1/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000508	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0000822	OMIM:614424	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:614424	Joubert syndrome 14		HP:0000426	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0000107	PMID:22152675	PCS		15/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000007	PMID:22152675	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000348	OMIM:614424	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614424	Joubert syndrome 14		HP:0000568	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0000648	PMID:22152675	PCS		1/14			P	HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0001510	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0000322	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614424	Joubert syndrome 14		HP:0000589	PMID:22152675	PCS		2/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:614424	Joubert syndrome 14		HP:0000369	OMIM:614424	TAS					P	HPO:skoehler[2012-10-17]
OMIM:148100	KELOIDS		HP:0010562	OMIM:148100	IEA					P	HPO:skoehler[2009-02-17]
OMIM:148100	KELOIDS		HP:0000006	OMIM:148100	IEA					I	HPO:iea[2009-02-17]
OMIM:609313	MEDNIK syndrome		HP:0002014	PMID:19057675	PCS	HP:0003577	6/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0001396	PMID:19057675	PCS		3/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0003577	PMID:19057675	PCS		6/6			C	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0000582	PMID:19057675	PCS		3/4			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0005235	PMID:19057675	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0004388	PMID:19057675	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0001263	PMID:19057675	PCS		5/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0001395	PMID:19057675	PCS		1/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0001252	PMID:19057675	PCS		5/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0002580	PMID:19057675	PCS		1/6			P	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0001394	PMID:19057675	PCS		2/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0010783	PMID:19057675	PCS		3/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0033643	PMID:19057675	PCS		4/4			P	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0008064	PMID:19057675	PCS		6/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0000518	PMID:19057675	PCS		2/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0003819	PMID:19057675	PCS		2/6			C	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0000407	PMID:19057675	PCS		5/6			P	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0009830	PMID:19057675	PCS		2/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0000007	PMID:19057675	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0000348	PMID:19057675	PCS		4/4			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0001522	PMID:19057675	PCS		1/6			C	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0003811	PMID:19057675	PCS		1/6			C	HPO:probinson[2022-08-28]
OMIM:609313	MEDNIK syndrome		HP:0001510	OMIM:609313	TAS					P	HPO:skoehler[2013-06-05]
OMIM:609313	MEDNIK syndrome		HP:0001249	PMID:19057675	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-08-28]
OMIM:185600	Symphalangism of toes		HP:0100235	OMIM:185600	TAS					P	HPO:probinson[2012-07-24]
OMIM:185600	Symphalangism of toes		HP:0000006	OMIM:185600	TAS					I	HPO:probinson[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0001265	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0003202	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0001310	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0001761	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0003487	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0001272	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0001284	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0002075	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0003690	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0003390	OMIM:607458	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607458	Spinocerebellar ataxia 18		HP:0000639	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0007240	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0011462	OMIM:607458	TAS					C	HPO:probinson[2022-09-04]
OMIM:607458	Spinocerebellar ataxia 18		HP:0000006	OMIM:607458	IEA					I	HPO:iea[2009-02-17]
OMIM:607458	Spinocerebellar ataxia 18		HP:0001337	OMIM:607458	IEA					P	HPO:iea[2009-02-17]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0007979	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000365	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0001591	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0001290	PMID:31092906	PCS		3/5			P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0001270	PMID:31092906	PCS					P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000218	PMID:31092906	PCS		2/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0001324	PMID:31092906	PCS					P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000358	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000457	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0003202	PMID:31092906	PCS					P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000297	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0008936	PMID:31092906	PCS		2/5			P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0008936	PMID:31092906	PCS	HP:0003593	4/5			P	HPO:probinson[2025-02-23]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0002015	PMID:31092906	PCS					P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0002650	PMID:31092906	PCS					P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0001288	PMID:31092906	PCS		4/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0001284	PMID:31092906	PCS		2/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0002093	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0012585	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000508	PMID:31092906	PCS		4/4			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0002803	PMID:31092906	PCS		1/4			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0001558	PMID:31092906	IEA		1/5			P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000007	PMID:31092906	PCS					I	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0002747	PMID:31092906	PCS					P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000325	PMID:31092906	PCS		2/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000347	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000369	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000028	PMID:31092906	PCS					P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000028	PMID:31092906	PCS		1/3	MALE		P	HPO:probinson[2020-06-14]
OMIM:618578	Myopathy, congenital, progressive, with scoliosis		HP:0000126	PMID:31092906	PCS		1/5			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:614342	Intellectual developmental disorder, autosomal recessive 30		HP:0000252	OMIM:614342	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614342	Intellectual developmental disorder, autosomal recessive 30		HP:0000007	OMIM:614342	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614342	Intellectual developmental disorder, autosomal recessive 30		HP:0000158	OMIM:614342	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614342	Intellectual developmental disorder, autosomal recessive 30		HP:0001510	OMIM:614342	TAS					P	HPO:skoehler[2017-07-13]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001650	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0002023	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001195	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001252	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0002162	OMIM:220210	TAS					P	HPO:skoehler[2014-02-06]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0004383	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001290	OMIM:220210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001629	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0002937	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000316	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000238	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000337	OMIM:220210	TAS		20/20			P	HPO:probinson[2012-05-01];HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001305	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000835	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001642	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000175	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000494	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001263	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0005280	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0007291	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001719	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000921	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001636	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000007	OMIM:220210	IEA					I	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000348	OMIM:220210	TAS					P	HPO:probinson[2012-05-01]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000824	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001159	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001511	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000047	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0001631	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000347	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000369	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000589	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000248	OMIM:220210	TAS					P	HPO:skoehler[2014-02-06]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000126	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:220210	Ritscher-Schinzel syndrome 1		HP:0000269	OMIM:220210	IEA					P	HPO:iea[2009-02-17]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0003596	PMID:11846417	PCS					C	HPO:probinson[2022-07-03]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0005110	PMID:22335739	PCS					P	HPO:probinson[2019-05-01];HPO:probinson[2019-05-01]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0001635	PMID:22335739	PCS					P	HPO:probinson[2019-05-01];HPO:probinson[2019-05-01]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0012664	PMID:22335739	PCS					P	HPO:probinson[2019-05-01]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0006699	PMID:11846417	PCS					P	HPO:probinson[2019-05-01]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0000006	PMID:11846417	PCS					I	HPO:skoehler[2013-01-10];HPO:probinson[2019-05-01]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0004756	PMID:22335739	PCS					P	HPO:probinson[2019-05-01];HPO:probinson[2019-05-01]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0001678	PMID:11846417	PCS					P	HPO:probinson[2019-05-01]
OMIM:604145	Cardiomyopathy, dilated, 1G		HP:0001644	PMID:22335739	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2019-05-01]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000494	OMIM:155145	IEA					P	HPO:iea[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000161	OMIM:155145	TAS					P	HPO:skoehler[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000193	OMIM:155145	IEA					P	HPO:iea[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0010609	OMIM:155145	IEA					P	HPO:skoehler[2010-06-20]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000316	OMIM:155145	IEA					P	HPO:iea[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000337	OMIM:155145	IEA					P	HPO:iea[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0100582	OMIM:155145	TAS					P	HPO:skoehler[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000612	OMIM:155145	IEA					P	HPO:iea[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000218	OMIM:155145	IEA					P	HPO:iea[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0000006	OMIM:155145	IEA					I	HPO:iea[2009-02-17]
OMIM:155145	Cleft, median, of upper lip with polyps of facial skin and nasal mucosa		HP:0006866	OMIM:155145	IEA					P	HPO:iea[2009-02-17]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001265	OMIM:615048	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0003202	PMID:22535186	PCS		4/5		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0003236	OMIM:615048	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0003596	PMID:22535186	PCS		4/5			C	HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001288	OMIM:615048	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001761	OMIM:615048	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0003394	PMID:22535186	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001284	PMID:22535186	PCS		5/5			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0002380	OMIM:615048	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0008981	OMIM:615048	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0002936	OMIM:615048	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0025710	PMID:22535186	PCS		1/5			C	HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0007269	PMID:22535186	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001324	PMID:22535186	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001763	OMIM:615048	TAS					P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0000006	PMID:22535186	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-13]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0003677	OMIM:615048	TAS					C	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001337	OMIM:615048	TAS		HP:0040283			P	HPO:skoehler[2013-06-05]
OMIM:615048	Spinal muscular atrophy, Jokela type		HP:0001765	OMIM:615048	TAS					P	HPO:skoehler[2013-06-05]
OMIM:619672	Spermatogenic failure 61		HP:0003251	PMID:31125047;PMID:32634216;PMID:31682730	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619672	Spermatogenic failure 61		HP:0000007	PMID:31125047	PCS					I	HPO:probinson[2022-02-12]
OMIM:619672	Spermatogenic failure 61		HP:0011961	PMID:31125047;PMID:32634216;PMID:31682730	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619672	Spermatogenic failure 61		HP:0031039	PMID:31125047;PMID:32634216;PMID:31682730	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000089	PMID:25728776	PCS		1/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0004322	PMID:25728776	PCS	HP:0003577	5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000122	PMID:25728776	PCS	HP:0003577	1/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0002186	PMID:25872942	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000086	PMID:25728776	PCS	HP:0003577	1/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001251	PMID:25872942	PCS	HP:0003581	2/2		HP:0003676	P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0003390	PMID:25872942	PCS	HP:0003581	2/2			P	HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000518	OMIM:616541	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000639	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000639	PMID:25872942	PCS	HP:0003581	2/2			P	HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001888	OMIM:616541	TAS				HP:0012825	P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000956	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001644	PMID:25872942	PCS	HP:0011462	1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000252	PMID:25728776	PCS	HP:0003577	5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000054	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000692	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000331	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000490	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001260	PMID:25872942	PCS	HP:0003581	2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001263	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0002075	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000407	OMIM:616541	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000007	PMID:25728776	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000601	PMID:25872942	PCS	HP:0003577	2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000444	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000763	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0003119	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000325	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000340	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001310	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000023	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0008070	OMIM:616541	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000819	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0100543	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001903	OMIM:616541	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000855	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0008873	PMID:25872942	PCS		2/2			P	HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0002119	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0030084	OMIM:616541	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000455	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001620	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0006855	OMIM:616541	TAS				HP:0012825	P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0002136	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0009826	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000750	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0003189	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000276	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001761	PMID:25872942	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001288	PMID:25872942	PCS	HP:0003581	2/2			P	HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000426	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0007772	PMID:25872942	PCS	HP:0003581	2/2			P	HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000348	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000821	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001956	OMIM:616541	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0001511	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0000028	PMID:25872942;PMID:25728776	PCS		12/12	MALE		P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0002721	OMIM:616541	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616541	Short stature, microcephaly, and endocrine dysfunction		HP:0009879	OMIM:616541	TAS					P	HPO:skoehler[2015-12-30]
OMIM:232600	Glycogen storage disease V		HP:0003236	PMID:22250184;PMID:21880526	PCS		172/174			P	HPO:probinson[2022-08-24];HPO:probinson[2012-04-26]
OMIM:232600	Glycogen storage disease V		HP:0003621	PMID:21880526	PCS		1/6			C	HP:probinson[2018-05-06];HPO:probinson[2022-08-24]
OMIM:232600	Glycogen storage disease V		HP:0003596	PMID:21880526	PCS		1/6			C	HPO:probinson[2022-08-24]
OMIM:232600	Glycogen storage disease V		HP:0003201	PMID:21880526	PCS		3/6			P	HPO:probinson[2022-08-24]
OMIM:232600	Glycogen storage disease V		HP:6000320	PMID:3476851	PCS		3/3			P	HPO:probinson[2024-02-27]
OMIM:232600	Glycogen storage disease V		HP:6000358	PMID:21880526	PCS		4/4			P	HPO:probinson[2024-02-27]
OMIM:232600	Glycogen storage disease V		HP:6000526	PMID:3476851	PCS					P	HPO:probinson[2024-04-03]
OMIM:232600	Glycogen storage disease V		HP:0009045	PMID:8316268	PCS					P	HP:probinson[2018-05-06]
OMIM:232600	Glycogen storage disease V		HP:0011463	PMID:21880526	PCS		4/6			C	HPO:probinson[2022-08-24];HPO:probinson[2022-08-24]
OMIM:232600	Glycogen storage disease V		HP:0002913	PMID:22250184;PMID:21880526	PCS		101/202			P	HPO:probinson[2022-08-24];HPO:iea[2009-02-17]
OMIM:232600	Glycogen storage disease V		HP:0003738	PMID:8316268	PCS					P	HPO:probinson[2012-04-26]
OMIM:232600	Glycogen storage disease V		HP:0000007	PMID:8316268	PCS					I	HPO:iea[2009-02-17]
OMIM:232600	Glycogen storage disease V		HP:0040319	OMIM:232600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:232600	Glycogen storage disease V		HP:0001324	PMID:22250184	PCS		49/196			P	HPO:skoehler[2010-06-20]
OMIM:232600	Glycogen storage disease V		HP:0003710	PMID:8316268	PCS					P	HPO:probinson[2012-04-26]
OMIM:232600	Glycogen storage disease V		HP:0002149	PMID:21880526	PCS		2/5			P	HPO:probinson[2022-08-24]
OMIM:232600	Glycogen storage disease V		HP:0003546	PMID:21880526	PCS					P	HPO:probinson[2022-08-24]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0003565	PMID:38609546	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0002573	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0002583	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0030057	PMID:38609546	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0410295	PMID:38609546	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0002240	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0003593	PMID:38609546	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0011850	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0011463	PMID:38609546	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0001954	PMID:38609546	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0002716	PMID:38609546	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0000007	PMID:38609546	PCS					I	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0000389	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0001744	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0006568	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0001369	PMID:38609546	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:620795	Autoinflammation with episodic fever and immune dysregulation		HP:0001974	PMID:38609546	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:611548	Premature ovarian failure 5		HP:0008209	PMID:17701902	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2021-10-13]
OMIM:611548	Premature ovarian failure 5		HP:0033085	PMID:21837770	PCS					P	HPO:probinson[2021-10-13]
OMIM:611548	Premature ovarian failure 5		HP:0000869	PMID:21837770	PCS		9/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-10-13]
OMIM:611548	Premature ovarian failure 5		HP:0010464	PMID:21837770	PCS		1/12			P	HPO:probinson[2021-10-13]
OMIM:611548	Premature ovarian failure 5		HP:0000006	PMID:17701902	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-13]
OMIM:611548	Premature ovarian failure 5		HP:0000786	PMID:21837770	PCS		3/12			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-10-13]
OMIM:611548	Premature ovarian failure 5		HP:0008724	PMID:21837770	PCS		5/12			P	HPO:probinson[2021-10-13]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0030205	PMID:23404334	PCS		4/4			P	HPO:probinson[2015-03-30]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0001288	PMID:23404334	PCS					P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-11]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0003473	PMID:23404334	PCS		2/2			P	HPO:probinson[2015-03-30]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0002828	PMID:23404334	PCS		6/7			P	HPO:probinson[2015-03-30]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0000508	PMID:23404334	PCS		1/7		HP:0012825	P	HPO:probinson[2015-03-30]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0000007	PMID:23404334	PCS					I	HPO:probinson[2015-03-30]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0002359	PMID:23404334	PCS					P	HPO:probinson[2015-03-30]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0030208	PMID:23404334	PCS		0/2			P	HPO:probinson[2015-03-30];HPO:probinson[2023-02-11]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0003677	PMID:23404334	PCS					C	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-11]
OMIM:616227	Myasthenic syndrome, congenital, 15		HP:0003403	PMID:23404334	PCS		5/5			P	HPO:probinson[2015-03-30]
OMIM:236300	Hooft disease		HP:0001507	OMIM:236300	IEA					P	HPO:iea[2009-02-17]
OMIM:236300	Hooft disease		HP:0001939	OMIM:236300	IEA					P	HPO:iea[2009-02-17]
OMIM:236300	Hooft disease		HP:0000007	OMIM:236300	IEA					I	HPO:iea[2009-02-17]
OMIM:236300	Hooft disease		HP:0000510	OMIM:236300	IEA					P	HPO:iea[2009-02-17]
OMIM:236300	Hooft disease		HP:0001249	OMIM:236300	IEA					P	HPO:iea[2009-02-17]
OMIM:236300	Hooft disease		HP:0001820	OMIM:236300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614430	Atrioventricular septal defect 4		HP:0003577	OMIM:614430	TAS					C	HPO:probinson[2023-01-16]
OMIM:614430	Atrioventricular septal defect 4		HP:0010445	OMIM:614430	TAS					P	HPO:skoehler[2013-06-11]
OMIM:614430	Atrioventricular septal defect 4		HP:0000006	OMIM:614430	TAS					I	HPO:skoehler[2012-10-17]
OMIM:617111	Macular dystrophy, patterned, 3		HP:0011506	PMID:26744326	PCS		HP:0040284			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617111	Macular dystrophy, patterned, 3		HP:0011462	PMID:26744326	PCS					C	HPO:probinson[2022-12-21]
OMIM:617111	Macular dystrophy, patterned, 3		HP:0007663	PMID:26744326	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-21]
OMIM:617111	Macular dystrophy, patterned, 3		HP:0007401	PMID:26744326	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-21]
OMIM:617111	Macular dystrophy, patterned, 3		HP:0000510	PMID:26744326	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-21]
OMIM:617111	Macular dystrophy, patterned, 3		HP:0000006	PMID:26744326	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-21]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001332	PMID:15159508	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001250	OMIM:618222	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001252	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0010544	PMID:15159508	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0000639	OMIM:618222	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0005949	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002119	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001348	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001347	OMIM:618222	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0003623	PMID:9837812	PCS		1/1			C	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002476	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0003621	PMID:15159508	PCS		1/1			C	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001288	OMIM:618222	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0003542	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0011968	PMID:9837812	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001260	PMID:15159508	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002033	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001263	OMIM:618222	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002151	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002171	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0012416	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002093	OMIM:618222	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0011923	PMID:15159508	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0011448	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0100660	OMIM:618222	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001639	OMIM:618222	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0000007	PMID:9837812	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002329	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002527	PMID:15159508	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0002104	OMIM:618222	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618222	Mitochondrial complex I deficiency, nuclear type 2		HP:0001612	PMID:9837812	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:611560	Joubert syndrome 7		HP:0003774	PMID:17558409	PCS	HP:0003621	6/7			P	HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0002365	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0001273	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0001251	PMID:17558409	PCS		7/7			P	HPO:probinson[2013-04-02];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0001290	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0002084	OMIM:611560	TAS					P	HPO:probinson[2013-04-02]
OMIM:611560	Joubert syndrome 7		HP:0000639	PMID:17558409	PCS		3/7			P	HPO:probinson[2013-04-02];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0000657	PMID:17558409	PCS		6/7			P	HPO:probinson[2013-04-02];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0002419	PMID:17558409	PCS		5/6			P	HPO:probinson[2013-01-09];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0002857	PMID:17558409	PCS		1/7			P	HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0002876	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0001249	PMID:17558409	PCS		6/7			P	HPO:probinson[2013-04-02];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0000556	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0002650	PMID:17558409	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0002871	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0001162	OMIM:611560	TAS	HP:0003577				P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0001263	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0002790	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0000090	PMID:17558409	PCS		6/7			P	HPO:probinson[2013-04-02];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0100259	OMIM:611560	TAS					P	HPO:probinson[2013-04-02]
OMIM:611560	Joubert syndrome 7		HP:0002508	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0000508	PMID:17558409	PCS		3/7			P	HPO:probinson[2013-04-02];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0000107	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611560	Joubert syndrome 7		HP:0000007	PMID:17558409	PCS					I	HPO:probinson[2013-04-02];HPO:probinson[2022-09-02]
OMIM:611560	Joubert syndrome 7		HP:0002789	OMIM:611560	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615706	Auriculocondylar syndrome 3		HP:0003577	PMID:24268655	PCS		9/9			C	HPO:probinson[2023-02-26]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000293	PMID:24268655	PCS					P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-26]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000193	PMID:24268655	PCS		2/9			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-26]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000162	PMID:24268655	PCS		1/9			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-26]
OMIM:615706	Auriculocondylar syndrome 3		HP:0030022	PMID:24268655	PCS		9/9			P	HPO:skoehler[2014-10-10]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000007	PMID:24268655	PCS					I	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-26]
OMIM:615706	Auriculocondylar syndrome 3		HP:0008751	PMID:24268655	PCS		1/9			P	HPO:skoehler[2014-04-04]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000656	PMID:24268655	PCS		1/9			P	HPO:probinson[2023-02-26]
OMIM:615706	Auriculocondylar syndrome 3		HP:0008513	PMID:24268655	PCS		1/9			P	HPO:skoehler[2014-04-04]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000278	PMID:24268655	PCS		4/9			P	HPO:skoehler[2014-04-04]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000402	PMID:24268655	PCS		1/9			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-26]
OMIM:615706	Auriculocondylar syndrome 3		HP:0000347	PMID:24268655	PCS		4/9			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-02-26]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0003202	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0002015	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0003487	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0002145	OMIM:612069	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0030223	OMIM:612069	TAS					P	HPO:skoehler[2015-01-20]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0001260	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0003584	PMID:18309045	PCS		3/3			C	HPO:probinson[2022-11-08]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0000734	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0000712	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0007354	PMID:18309045	PCS	HP:0003584	3/3			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-11-08]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0000733	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0002747	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0001324	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0000741	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0001257	OMIM:612069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0000006	PMID:18309045	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:612069	Amyotrophic lateral sclerosis 10 with or without frontotemporal dementia		HP:0003678	OMIM:612069	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614418	Febrile seizures, familial, 11		HP:0002069	PMID:21922598	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:614418	Febrile seizures, familial, 11		HP:0002373	PMID:21922598	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:614418	Febrile seizures, familial, 11		HP:0002384	PMID:21922598	PCS	HP:0011462	1/4			P	HPO:probinson[2020-08-09]
OMIM:614418	Febrile seizures, familial, 11		HP:0000007	PMID:21922598	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:614418	Febrile seizures, familial, 11		HP:0410170	PMID:21922598	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-09]
OMIM:613411	Oguchi disease-2		HP:0000007	PMID:17070587	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-23]
OMIM:613411	Oguchi disease-2		HP:0007642	PMID:17070587	PCS					P	HPO:skoehler[2013-02-26];HPO:probinson[2020-07-23]
OMIM:613411	Oguchi disease-2		HP:0030824	PMID:17070587	PCS					P	HPO:probinson[2020-07-23]
OMIM:601001	Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive		HP:0003577	PMID:7526933	PCS		1/1			C	HPO:skoehler[2010-06-19];HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive		HP:0001805	PMID:7526933	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive		HP:0008066	PMID:7526933;PMID:7525408	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive		HP:0001807	PMID:7526933	PCS		0/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive		HP:0003593	PMID:7526933	PCS		2/2			C	HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive		HP:0000007	PMID:7526933	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive		HP:0200097	PMID:7526933	PCS		0/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex, autosomal recessive 1		HP:0034193	PMID:7526933;PMID:7525408	PCS		3/3			P	HPO:probinson[2022-05-14]
OMIM:601001	Epidermolysis bullosa simplex, autosomal recessive 1		HP:0032449	PMID:7526933	PCS		0/2			P	HPO:probinson[2022-05-14]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0000495	PMID:16652336	PCS		7/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-04]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0003621	PMID:16652336	PCS		1/7			C	HPO:probinson[2022-03-04]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0003596	PMID:16652336	PCS		1/7			C	HPO:probinson[2022-03-04]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0007690	PMID:16652336	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0001131	PMID:16652336	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-04]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0011462	PMID:16652336	PCS		5/7			C	HPO:probinson[2022-03-04]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0007663	PMID:16652336	PCS		1/7			P	HPO:probinson[2022-03-04]
OMIM:121820	Corneal dystrophy, epithelial basement membrane		HP:0000006	PMID:16652336	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:300842	Mcleod syndrome		HP:0003236	PMID:11761473	PCS		22/22			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001332	PMID:11761473	PCS		5/13			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0003198	PMID:11761473	PCS		8/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001250	PMID:11761473	PCS		6/12			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0005110	PMID:11761473	PCS		5/22			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0002240	PMID:11761473	PCS		5/12			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0031964	PMID:11761473	PCS		5/15			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0000716	PMID:11761473	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0012075	PMID:11761473	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001927	PMID:11761473	PCS		22/22			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0000739	PMID:11761473	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0007002	OMIM:300842	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300842	Mcleod syndrome		HP:0025435	PMID:11761473	PCS		10/11			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001324	PMID:11761473	PCS		13/20			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001744	PMID:11761473	PCS		5/13			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001644	PMID:11761473	PCS		2/22			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0020181	PMID:11761473	PCS		4/5			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0031956	PMID:11761473	PCS		5/15			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0003201	OMIM:300842	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300842	Mcleod syndrome		HP:0002197	OMIM:300842	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300842	Mcleod syndrome		HP:0001260	PMID:11761473	PCS		10/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0006938	PMID:11761473	PCS		6/15			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0003581	PMID:11761473	PCS		22/22			C	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0002072	PMID:11761473	PCS		18/19			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0030948	PMID:11761473	PCS		4/12			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0100660	OMIM:300842	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300842	Mcleod syndrome		HP:0012046	PMID:11761473	PCS		8/21			P	HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0000722	PMID:11761473	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001638	PMID:11761473	PCS		4/22			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0001417	PMID:11761473	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:300842	Mcleod syndrome		HP:0003438	PMID:11761473	PCS		18/20			P	HPO:probinson[2022-03-28]
OMIM:617663	Deafness, autosomal dominant 73		HP:0003621	PMID:29309402	PCS		6/7			C	HPO:probinson[2023-03-31]
OMIM:617663	Deafness, autosomal dominant 73		HP:0000407	PMID:29309402	PCS		7/7			P	HPO:probinson[2023-03-31]
OMIM:617663	Deafness, autosomal dominant 73		HP:0011463	PMID:29309402	PCS		1/7			C	HPO:probinson[2023-03-31]
OMIM:617663	Deafness, autosomal dominant 73		HP:0000006	PMID:29309402	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-31]
OMIM:618550	Oocyte maturation defect 7		HP:0032571	PMID:30918116	PCS					P	HPO:probinson[2020-03-14]
OMIM:618550	Oocyte maturation defect 7		HP:0008222	PMID:30918116	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618550	Oocyte maturation defect 7		HP:0000006	PMID:30918116	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:180750	Robinow-Sorauf syndrome		HP:0001363	PMID:10465122	PCS		2/2			P	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0000494	PMID:10465122	PCS		2/2			P	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0003189	OMIM:180750	TAS					P	HPO:probinson[2012-05-01]
OMIM:180750	Robinow-Sorauf syndrome		HP:0000486	OMIM:180750	IEA					P	HPO:iea[2009-02-17]
OMIM:180750	Robinow-Sorauf syndrome		HP:0000460	OMIM:180750	TAS					P	HPO:probinson[2012-05-01]
OMIM:180750	Robinow-Sorauf syndrome		HP:0000272	OMIM:180750	IEA					P	HPO:iea[2009-02-17]
OMIM:180750	Robinow-Sorauf syndrome		HP:0003593	PMID:10465122	PCS		1/1			C	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0011325	PMID:10465122	PCS		1/2			P	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0012368	OMIM:180750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:180750	Robinow-Sorauf syndrome		HP:0011304	PMID:10465122	PCS		1/2			P	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0010084	PMID:10465122	PCS		2/2			P	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0010055	PMID:10465122	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0000316	OMIM:180750	IEA					P	HPO:iea[2009-02-17]
OMIM:180750	Robinow-Sorauf syndrome		HP:0001822	PMID:10465122	PCS		2/2			P	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0001357	PMID:10465122	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0001488	PMID:10465122	PCS		2/2			P	HPO:probinson[2023-01-16]
OMIM:180750	Robinow-Sorauf syndrome		HP:0000586	OMIM:180750	IEA					P	HPO:iea[2009-02-17]
OMIM:180750	Robinow-Sorauf syndrome		HP:0000006	PMID:10465122	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-16]
OMIM:173800	Poland syndrome		HP:0001651	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0005256	OMIM:173800	TAS					P	HPO:probinson[2012-06-22]
OMIM:173800	Poland syndrome		HP:0005255	OMIM:173800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:173800	Poland syndrome		HP:0011959	OMIM:173800	TAS					P	HPO:probinson[2012-06-22]
OMIM:173800	Poland syndrome		HP:0000902	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0009011	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0002937	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0006230	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0030241	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0009026	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0000769	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0000912	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0001159	OMIM:173800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:173800	Poland syndrome		HP:0000773	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0000006	OMIM:173800	IEA					I	HPO:iea[2009-02-17]
OMIM:173800	Poland syndrome		HP:0006008	OMIM:173800	IEA					P	HPO:iea[2009-02-17]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000121	PMID:17033971	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0003774	PMID:17033971	PCS		8/12			P	HPO:probinson[2023-02-26];HPO:probinson[2024-03-08]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000483	OMIM:248190	IEA					P	HPO:skoehler[2019-02-22]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0003621	PMID:17033971	PCS		2/12			C	HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000010	PMID:17033971	PCS		8/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0005567	PMID:17033971	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000486	OMIM:248190	IEA					P	HPO:skoehler[2019-02-22]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0004363	PMID:17033971	PCS		0/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0012608	PMID:17033971	PCS		12/12			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-08]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0003593	PMID:17033971	PCS		8/12			C	HPO:probinson[2023-02-26];HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0002150	PMID:17033971	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0012637	OMIM:248190	TAS					P	HPO:skoehler[2014-01-28]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0012622	PMID:17033971	PCS					P	HPO:probinson[2014-01-18];HPO:probinson[2024-03-08]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000705	OMIM:248190	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0002917	PMID:17033971	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000639	PMID:17033971	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0011463	PMID:17033971	PCS		2/12			C	HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000007	PMID:17033971	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000510	OMIM:248190	IEA					P	HPO:iea[2009-02-17]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000545	PMID:17033971	PCS		10/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0000787	PMID:17033971	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:248190	Hypomagnesemia 5, renal, with or without ocular involvement		HP:0001116	PMID:17033971	PCS		5/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:615074	GAND syndrome		HP:0002465	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0002463	PMID:23644463	PCS		4/4			P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0000486	PMID:23644463	PCS		4/4			P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0000540	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000581	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0003593	OMIM:615074	TAS					C	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0008070	PMID:23644463	PCS		4/4			P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0100033	OMIM:615074	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000316	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000337	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0100807	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000219	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000455	PMID:23644463	PCS		4/4			P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0000752	OMIM:615074	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000154	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000431	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0000490	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0001263	PMID:23644463	PCS		4/4			P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0010511	OMIM:615074	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615074	GAND syndrome		HP:0045025	OMIM:615074	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615074	GAND syndrome		HP:0000748	PMID:23644463	PCS					P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0001319	PMID:23644463	PCS					P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0000322	PMID:23644463	PCS		4/4			P	HPO:probinson[2015-03-28]
OMIM:615074	GAND syndrome		HP:0000006	PMID:23644463	PCS					I	HPO:probinson[2015-03-28]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0003510	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0006406	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0001156	PMID:7550321	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0003311	PMID:7550321	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0000023	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0003375	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0003173	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0011860	OMIM:184250	TAS					P	HPO:probinson[2012-05-26]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0008873	PMID:7550321	PCS		2/2			P	HPO:probinson[2022-12-21]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0002812	PMID:7550321	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0003307	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0030084	PMID:7550321	PCS		1/2			P	HPO:probinson[2022-12-21]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0002857	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0001763	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0001249	PMID:7550321	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0000175	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0002650	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0003025	OMIM:184250	TAS					P	HPO:probinson[2012-05-26]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0002651	OMIM:184250	IEA					P	HPO:skoehler[2015-01-27]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0003320	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0000907	OMIM:184250	TAS					P	HPO:probinson[2012-06-10]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0000926	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0000768	PMID:7550321	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0001538	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0008788	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0000006	PMID:7550321	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:184250	Spondyloepimetaphyseal dysplasia, Strudwick type		HP:0000545	OMIM:184250	IEA					P	HPO:iea[2009-02-17]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002069	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0001254	OMIM:617105	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0000121	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002521	PMID:27476654	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002188	PMID:27476654	PCS		2/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002540	OMIM:617105	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0000684	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0001371	OMIM:617105	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0003593	PMID:27476654	PCS		1/3			C	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0001290	PMID:27476654	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0032794	PMID:27476654	PCS		3/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0011167	PMID:27476654	PCS		2/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0000737	OMIM:617105	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0003623	PMID:27476654	PCS		2/3			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002751	OMIM:617105	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0008936	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002059	PMID:27476654	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0000252	PMID:27476654	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0001344	OMIM:617105	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002353	PMID:27476654	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002376	OMIM:617105	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002079	PMID:27476654	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0003487	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0011968	OMIM:617105	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0010818	PMID:27476654	PCS		2/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0001263	PMID:27476654	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0002273	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0031475	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0032667	PMID:27476654	PCS		2/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0011097	PMID:27476654	PCS		1/3			P	HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0200134	PMID:27476654	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0001257	OMIM:617105	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617105	Epileptic encephalopathy, early infantile, 41		HP:0000006	PMID:27476654	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0001298	PMID:18306244	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0003198	OMIM:618236	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0001250	PMID:18306244	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0200128	PMID:18306244	PCS		3/3			P	HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0002151	PMID:18306244	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0001263	PMID:18306244	PCS		4/4			P	HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0005484	PMID:18306244	PCS		4/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0001290	PMID:18306244	PCS		3/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0011923	PMID:18306244	PCS		4/4			P	HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0012444	PMID:18306244	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0000639	PMID:18306244	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0001639	PMID:18306244	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0000007	PMID:18306244	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0000648	PMID:18306244	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0002104	PMID:18306244	PCS		3/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0003128	PMID:18306244	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-10]
OMIM:618236	Mitochondrial complex I deficiency, nuclear type 14		HP:0003623	PMID:18306244	PCS		7/7			C	HPO:probinson[2022-12-10]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0003236	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0008948	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0001288	OMIM:601954	TAS					P	HPO:probinson[2012-05-26]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0003551	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0003560	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0009053	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0008981	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0009025	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0009046	OMIM:601954	TAS					P	HPO:probinson[2012-05-26]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0009027	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0000007	OMIM:601954	IEA					I	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0003805	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0002522	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0003557	OMIM:601954	IEA					P	HPO:iea[2009-02-17]
OMIM:601954	Muscular dystrophy, limb-girdle, type 2G		HP:0008944	OMIM:601954	TAS					P	HPO:probinson[2012-05-26]
OMIM:178000	Pterygium of conjunctiva and cornea		HP:0000502	OMIM:178000	IEA					P	HPO:iea[2009-02-17]
OMIM:178000	Pterygium of conjunctiva and cornea		HP:0001059	OMIM:178000	TAS					P	HPO:probinson[2009-02-17]
OMIM:178000	Pterygium of conjunctiva and cornea		HP:0000006	OMIM:178000	TAS					I	HPO:probinson[2009-02-17]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0002653	PMID:20335586	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0004322	PMID:20335586	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0003165	PMID:20335586	PCS		0/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0000083	PMID:20335586	PCS	HP:0003581	2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0003076	PMID:20335586	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0002150	PMID:20335586	PCS	HP:0011463	2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0000093	PMID:20335586	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0012213	PMID:20335586	PCS	HP:0003581	2/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0031415	PMID:20335586	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0002909	PMID:20335586	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0011463	PMID:20335586	PCS		2/2			C	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0000938	PMID:20335586	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0002748	PMID:20335586	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0000007	PMID:20335586	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0000117	PMID:20335586	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0002749	PMID:20335586	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0002757	PMID:20335586	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0000114	PMID:20335586	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-12]
OMIM:613388	Fanconi renotubular syndrome 2		HP:0002148	PMID:20335586	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001250	PMID:17632511	PCS		1/6			P	HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0003034	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001293	OMIM:259710	TAS					P	HPO:skoehler[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0003593	PMID:17632511	PCS		3/6			C	HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0011002	OMIM:259710	TAS					P	HPO:skoehler[2015-01-27]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0000639	PMID:17632511	PCS		2/6			P	HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001903	PMID:17632511	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0000618	PMID:17632511	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0000238	PMID:17632511	PCS		3/6			P	HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0002757	PMID:17632511	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0002857	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0006335	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001249	PMID:17632511	PCS		0/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0004437	OMIM:259710	IEA					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0002754	OMIM:259710	TAS					P	HPO:skoehler[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0003623	PMID:17632511	PCS		3/6			C	HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0007626	OMIM:259710	TAS					P	HPO:skoehler[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0007209	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0000670	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0004499	OMIM:259710	IEA					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0030328	PMID:17632511	PCS		4/4			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0000007	PMID:17632511	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0000648	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001978	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001873	OMIM:259710	TAS					P	HPO:skoehler[2014-01-28]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001433	PMID:17632511	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0001876	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:259710	Osteopetrosis, autosomal recessive 2		HP:0000303	OMIM:259710	TAS					P	HPO:iea[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0003016	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0003577	PMID:34347384	PCS		1/1			C	HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0006429	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0001596	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0010109	OMIM:135100	TAS					P	HPO:skoehler[2013-10-22]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0003155	PMID:17077940	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0010566	OMIM:135100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:6000952	PMID:33364240	PCS					P	HPO:probinson[2024-08-04]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0010034	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0010054	OMIM:135100	TAS					P	HPO:probinson[2013-04-07]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0001822	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0001822	PMID:17077940	PCS	HP:0003577	1/1			P	HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0001822	PMID:34347384	PCS	HP:0003577	1/1			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0002878	OMIM:135100	TAS					P	HPO:skoehler[2014-06-24]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0002135	OMIM:135100	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0005986	PMID:34347384	PCS	HP:0011463	1/1			P	HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0002650	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0011987	PMID:16642017	PCS	HP:0003593	1/1			P	HPO:probinson[2012-07-19];HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0011987	PMID:34347384	PCS		1/1			P	HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0011988	OMIM:135100	TAS					P	HPO:probinson[2012-07-19]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0011989	OMIM:135100	TAS					P	HPO:probinson[2012-07-19]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0002093	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0000407	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0004629	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0004209	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0000405	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0000006	PMID:16642017	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-02]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0008449	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:135100	Fibrodysplasia ossificans progressiva		HP:0000687	OMIM:135100	TAS					P	HPO:probinson[2009-02-17]
OMIM:302700	Cerebral sclerosis, diffuse, Scholz type		HP:0003621	OMIM:302700	IEA					C	HPO:iea[2009-02-17]
OMIM:302700	Cerebral sclerosis, diffuse, Scholz type		HP:0000365	OMIM:302700	IEA					P	HPO:iea[2009-02-17]
OMIM:302700	Cerebral sclerosis, diffuse, Scholz type		HP:0000726	OMIM:302700	IEA					P	HPO:iea[2009-02-17]
OMIM:302700	Cerebral sclerosis, diffuse, Scholz type		HP:0007340	OMIM:302700	IEA					P	HPO:skoehler[2010-06-24]
OMIM:302700	Cerebral sclerosis, diffuse, Scholz type		HP:0000618	OMIM:302700	IEA					P	HPO:iea[2009-02-17]
OMIM:302700	Cerebral sclerosis, diffuse, Scholz type		HP:0001417	OMIM:302700	IEA					I	HPO:iea[2009-02-17]
OMIM:302700	Cerebral sclerosis, diffuse, Scholz type		HP:0001258	OMIM:302700	IEA					P	HPO:iea[2009-02-17]
OMIM:612096	Otosclerosis 8		HP:0000362	OMIM:612096	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612096	Otosclerosis 8		HP:0000365	OMIM:612096	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612096	Otosclerosis 8		HP:0000006	OMIM:612096	IEA					I	HPO:skoehler[2010-06-19]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000044	PMID:22036172;PMID:22036171;PMID:28589944	PCS		5/7			P	HPO:probinson[2022-03-11];HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0003577	PMID:28589944	IEA		1/1			C	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000684	PMID:22036172	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001310	PMID:28589944;OMIM:614381	PCS		11/11			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0004322	OMIM:614381	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001332	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001272	PMID:22036171;PMID:28589944	PCS		5/5			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001151	PMID:22036171	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0002066	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001251	PMID:22036172;PMID:22036171;PMID:28589944	PCS		8/8			P	HPO:probinson[2022-03-11];HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0006808	OMIM:614381	IEA					P	HPO:probinson[2013-08-10]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0002080	PMID:22036171;PMID:28589944	PCS		4/5			P	HPO:probinson[2022-03-11];HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0033725	PMID:22036172;PMID:28589944	PCS		4/4			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0011463	PMID:22036172;PMID:22036171	PCS		7/7			C	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0003429	PMID:22036172;PMID:28589944	PCS		4/4			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0002415	PMID:22036171;PMID:28589944	PCS		5/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-11];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001249	PMID:22036171	PCS		4/4			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000677	PMID:22036172	PCS		2/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001347	OMIM:614381	IEA					P	HPO:probinson[2013-08-10]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0006855	PMID:22036172	PCS		3/3			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0002015	PMID:22036171	PCS		1/4			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000695	PMID:22036172	PCS		2/3			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000750	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0002079	PMID:22036171	PCS		4/4			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001260	PMID:28589944;OMIM:614381	PCS		11/11			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001263	PMID:22036172;PMID:28589944	PCS		4/4			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0002075	PMID:22036171	PCS		4/4			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0011003	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0002827	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000668	PMID:22036171	PCS		0/4			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000007	PMID:22036171	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0007256	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000648	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001257	PMID:22036172;PMID:22036171	PCS		3/7			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001510	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000666	PMID:22036171	PCS		2/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0000545	PMID:22036171	PCS		3/4			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-03-11]
OMIM:614381	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism		HP:0001337	PMID:28589944	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:146850	Immune suppression		HP:0002715	OMIM:146850	IEA					P	HPO:iea[2009-02-17]
OMIM:146850	Immune suppression		HP:0000006	OMIM:146850	IEA					I	HPO:iea[2009-02-17]
OMIM:131400	Eosinophilia, familial		HP:0002113	PMID:6033105	PCS		HP:0040282			P	HPO:lccarmody[2018-10-04];HP:probinson[2019-01-03]
OMIM:131400	Eosinophilia, familial		HP:0001880	PMID:9758611;OMIM:131400	PCS		20/20			P	HPO:lccarmody[2018-10-04];HPO:iea[2009-02-17]
OMIM:131400	Eosinophilia, familial		HP:0001903	PMID:9758611	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:131400	Eosinophilia, familial		HP:0002837	PMID:6033105	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:131400	Eosinophilia, familial		HP:0031323	PMID:9758611	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:131400	Eosinophilia, familial		HP:0001873	PMID:6033105	PCS		HP:0040283			P	HPO:lccarmody[2018-10-04];HP:probinson[2019-01-03]
OMIM:131400	Eosinophilia, familial		HP:0000006	OMIM:131400	IEA					I	HPO:iea[2009-02-17]
OMIM:131400	Eosinophilia, familial		HP:0001974	PMID:9758611;PMID:6033105	PCS		20/20			P	HPO:lccarmody[2018-10-04]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001276	PMID:35830857	PCS		10/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0003577	PMID:30214071;PMID:35830857	PCS		19/19			C	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002521	PMID:35830857	PCS		4/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0000365	PMID:35830857	PCS		4/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0000122	PMID:30214071	PCS		1/3			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001332	PMID:35830857	PCS		3/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0004322	PMID:35830857	PCS		7/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002384	PMID:35830857	PCS		1/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002120	PMID:35830857	PCS		3/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001252	PMID:35830857	PCS		5/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0032794	PMID:35830857	PCS		6/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002282	PMID:35830857	PCS		1/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001270	PMID:35830857	PCS		15/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0000639	PMID:35830857	PCS		4/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001508	PMID:35830857	PCS		8/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001629	PMID:35830857	PCS		2/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0006970	PMID:30214071	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002119	PMID:35830857	PCS		1/9			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001643	PMID:30214071;PMID:35830857	PCS		7/19			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001302	PMID:35830857	PCS		3/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002514	PMID:35830857	PCS		9/9			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0007305	PMID:30214071	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001249	PMID:35830857	PCS		15/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001320	PMID:35830857	PCS		2/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0000252	PMID:35830857	PCS		15/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002510	PMID:35830857	PCS		6/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001344	PMID:35830857	PCS		15/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002079	PMID:35830857	PCS		7/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002197	PMID:35830857	PCS		7/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0011968	PMID:35830857	PCS		7/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0002352	PMID:35830857	PCS		11/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001263	PMID:35830857	PCS		15/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0011641	PMID:35830857	PCS		1/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0011097	PMID:35830857	PCS		7/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0033140	PMID:35830857	PCS		1/14			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001518	PMID:35830857	PCS		9/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0011451	PMID:30214071	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0011330	PMID:30214071	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0032792	PMID:35830857	PCS		3/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0000007	PMID:30214071	PCS					I	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0007334	PMID:35830857	PCS		2/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0003811	PMID:30214071	PCS		1/3			C	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0001631	PMID:30214071;PMID:35830857	PCS		4/19			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0007359	PMID:35830857	PCS		11/16			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0000028	PMID:35830857	PCS		3/10			P	HPO:probinson[2022-09-05]
OMIM:620024	Neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities		HP:0006821	PMID:35830857	PCS		1/14			P	HPO:probinson[2022-09-05]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0003621	PMID:26691986	PCS		1/9			C	HPO:probinson[2023-06-09]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0003596	PMID:26691986	PCS		7/9			C	HPO:probinson[2023-06-09]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0008001	PMID:26691986	PCS		3/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-09]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0011462	PMID:26691986	PCS		1/9			C	HPO:probinson[2023-06-09]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0007663	PMID:26691986	PCS		6/9			P	HPO:probinson[2023-06-09]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0011510	OMIM:608970	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0007963	PMID:26691986	PCS		11/14			P	HPO:probinson[2023-06-09]
OMIM:608970	Macular dystrophy, butterfly-shaped pigmentary, 2		HP:0000006	PMID:26691986	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:606785	Crigler-Najjar syndrome, type II		HP:0008282	PMID:8276413;PMID:9621515	PCS		8/8			P	HPO:probinson[2024-03-10];HPO:probinson[2009-02-17];HPO:probinson[2024-03-10]
OMIM:606785	Crigler-Najjar syndrome, type II		HP:0000007	PMID:8276413	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:606785	Crigler-Najjar syndrome, type II		HP:0002910	PMID:9621515	PCS		0/7			P	HPO:probinson[2012-07-20];HPO:probinson[2024-03-10]
OMIM:606785	Crigler-Najjar syndrome, type II		HP:6000617	PMID:7989595	PCS					P	HPO:probinson[2024-04-03]
OMIM:606785	Crigler-Najjar syndrome, type II		HP:0000952	PMID:9621515	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000341	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0002389	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0003577	PMID:33442026	PCS		3/3			C	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000365	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0004322	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0011555	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0011833	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0002280	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0010442	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0045075	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0008070	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0001508	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000639	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000518	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0011220	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000218	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0001643	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000278	PMID:33442026	PCS		3/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0001320	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000252	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0006956	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000076	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000233	PMID:33442026	PCS		3/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0002079	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0002198	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0045025	PMID:33442026	PCS		3/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0011344	PMID:33442026	PCS		3/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0001518	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0001636	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000007	PMID:33442026	PCS					I	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000647	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0000543	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0001159	PMID:33442026	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:619869	Neurocardiofaciodigital syndrome		HP:0001631	PMID:33442026	PCS		1/3			P	HPO:probinson[2022-08-07]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0001880	OMIM:202700	IEA					P	HPO:iea[2009-02-17]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0001894	OMIM:202700	IEA					P	HPO:iea[2009-02-17]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0012311	OMIM:202700	TAS					P	HPO:skoehler[2013-08-18]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0001507	OMIM:202700	IEA					P	HPO:iea[2009-02-17]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0005541	OMIM:202700	TAS					P	HPO:probinson[2012-07-16]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0001903	OMIM:202700	TAS				HP:0012825	P	HPO:skoehler[2014-03-24]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0002718	PMID:19036076	TAS	HP:0003593				P	HPO:probinson[2012-07-16];HPO:probinson[2020-04-22]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0003593	PMID:1861198	TAS					C	HPO:skoehler[2014-03-24];HPO:probinson[2020-04-22]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0010702	OMIM:202700	IEA					P	HPO:iea[2009-02-17]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0004845	OMIM:202700	IEA					P	HPO:iea[2009-02-17]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0000006	PMID:14962902	PCS					I	HPO:skoehler[2014-03-24];HP:probinson[2019-03-01]
OMIM:202700	Neutropenia, severe congenital, 1, autosomal dominant		HP:0001875	PMID:14962902	PCS	HP:0003577				P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:615935	Pancreatic agenesis 2		HP:0000819	PMID:24212882	PCS		14/14			P	HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0003621	PMID:24212882	PCS		2/14			C	HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0001518	PMID:24212882	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0002594	PMID:24212882	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0001738	PMID:24212882	PCS		14/14			P	HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0011342	PMID:24212882	PCS		1/14			P	HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0011462	PMID:24212882	PCS		1/14			C	HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0002570	PMID:24212882	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0100801	PMID:24212882	PCS		4/9			P	HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0003593	PMID:24212882	PCS		3/14			C	HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0000007	PMID:24212882	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:615935	Pancreatic agenesis 2		HP:0003623	PMID:24212882	PCS		8/14			C	HPO:probinson[2023-02-25]
OMIM:206200	Iron-Refractory iron deficiency anemia		HP:0011273	PMID:18408718	PCS					P	HPO:probinson[2017-12-12]
OMIM:206200	Iron-Refractory iron deficiency anemia		HP:0004840	PMID:18408718	PCS					P	HPO:probinson[2013-12-19]
OMIM:206200	Iron-Refractory iron deficiency anemia		HP:0000007	PMID:18408718	PCS					I	HPO:skoehler[2009-02-17]
OMIM:206200	Iron-Refractory iron deficiency anemia		HP:0004447	PMID:18408718	PCS					P	HPO:probinson[2017-12-12]
OMIM:206200	Iron-Refractory iron deficiency anemia		HP:0031877	PMID:23729726	PCS					P	HPO:lccarmody[2018-09-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000486	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0004322	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0010296	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000476	PMID:32031333	PCS	HP:0011461	1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0003623	PMID:32031333	PCS		2/14			C	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002553	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002311	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000252	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000494	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000010	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0033454	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001182	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0008081	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0010952	PMID:32031333	PCS	HP:0011461	2/14			P	HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000407	PMID:32031333	PCS		1/13			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000646	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000767	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000403	PMID:32031333	PCS		3/13			P	HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000527	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001334	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000006	PMID:32031333	PCS					I	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000369	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0004689	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000582	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0003577	PMID:32031333	PCS		6/14			C	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0010945	PMID:32031333	PCS	HP:0011461	1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000463	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001274	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0008070	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000739	PMID:32031333	PCS		3/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000337	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000219	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000455	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0200085	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001562	PMID:32031333	PCS	HP:0011461	1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001320	PMID:32031333	PCS		3/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001561	PMID:32031333	PCS	HP:0011461	2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002650	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002099	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000508	PMID:32031333	PCS		3/26			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001558	PMID:32031333	PCS	HP:0011461	1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000348	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0100716	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0004704	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001555	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002007	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0007018	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000347	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001252	PMID:32031333	PCS		9/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000041	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0045075	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0100842	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0009381	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000319	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000718	PMID:32031333	PCS		4/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0011461	PMID:32031333	PCS		6/14			C	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000316	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000954	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001769	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001643	PMID:32031333	PCS		1/10			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001488	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001763	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001249	PMID:32031333	PCS		7/11			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000054	PMID:32031333	PCS		2/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0030820	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002870	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000293	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001382	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001263	PMID:32031333	PCS		9/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000294	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0011327	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0012541	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000729	PMID:32031333	PCS		9/13			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002509	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001137	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000047	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000322	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001655	PMID:32031333	PCS		1/10			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000687	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0005338	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0010627	PMID:32031333	PCS		1/12			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0009765	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000537	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0004736	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001500	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000894	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000256	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000154	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000276	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002572	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0009909	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0045025	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0005280	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0010579	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0032592	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0006485	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000426	PMID:32031333	PCS		2/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0002209	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001511	PMID:32031333	PCS	HP:0011461	1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000664	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000268	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001357	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000421	PMID:32031333	PCS		1/13			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000028	PMID:32031333	PCS		4/11			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0000303	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:619841	Chilton-Okur-Chung neurodevelopmental syndrome		HP:0001238	PMID:32031333	PCS		1/14			P	HPO:probinson[2022-06-25]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0002069	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0002078	PMID:31104773	PCS		3/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0002384	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0010819	PMID:31104773	IEA		2/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0002066	PMID:31104773	PCS		3/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0011149	PMID:31104773	PCS		2/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0001290	PMID:31104773	PCS		4/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0002072	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0002392	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0010850	PMID:31104773	PCS		2/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0007270	PMID:31104773	PCS		2/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0000729	PMID:31104773	PCS		2/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0430028	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0000219	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0011170	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0000006	PMID:31104773	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0001249	PMID:31104773	PCS		4/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0001337	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0002500	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:618587	Intellectual developmental disorder 60 with seizures		HP:0001336	PMID:31104773	PCS		1/4			P	HPO:probinson[2020-06-27]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0008209	PMID:34942119	PCS		1/7	FEMALE		P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000486	PMID:34942119	PCS		5/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000365	PMID:34942119	PCS		5/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0001263	PMID:34942119	PCS		11/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0001252	PMID:34942119	PCS		8/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0003593	PMID:34942119	PCS					C	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0001270	PMID:34942119	PCS					P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000316	PMID:34942119	PCS		6/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000767	PMID:34942119	PCS		7/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000007	PMID:34942119	PCS					I	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000218	PMID:34942119	PCS		3/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0007687	PMID:34942119	PCS		1/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000347	PMID:34942119	PCS		6/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000776	PMID:34942119	PCS		1/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0000402	PMID:34942119	PCS		1/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0001655	PMID:34942119	PCS		1/11			P	HPO:probinson[2022-03-19]
OMIM:619699	Ferguson-Bonni neurodevelopmental syndrome		HP:0025516	PMID:34942119	PCS		1/11			P	HPO:probinson[2022-03-19]
OMIM:300895	Ohdo syndrome, X-linked		HP:0004325	PMID:23395478	PCS		1/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000286	PMID:23395478	PCS		5/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000365	PMID:23395478	PCS		3/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000046	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000486	PMID:23395478	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001250	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000160	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001252	PMID:23395478	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000280	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0045075	PMID:23395478	PCS		5/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000639	PMID:23395478	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000957	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000319	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0011220	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000717	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000316	PMID:23395478	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001845	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0002019	PMID:23395478	PCS		2/5			P	HPO:probinson[2022-12-05];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001249	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000358	PMID:23395478	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0002036	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000494	PMID:23395478	PCS		0/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000054	PMID:23395478	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001385	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001344	PMID:23395478	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0011968	PMID:23395478	PCS		4/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001382	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001263	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000691	PMID:23395478	PCS		2/4			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0032524	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0009890	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0001419	PMID:23395478	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000448	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000568	PMID:23395478	PCS		3/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0009778	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000369	PMID:23395478	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000402	PMID:23395478	PCS		4/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000325	PMID:23395478	PCS		5/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000687	PMID:23395478	PCS		1/4			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000049	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000343	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000540	PMID:23395478	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000023	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000581	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0009487	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0008551	PMID:23395478	PCS		2/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000414	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0030084	PMID:23395478	PCS		2/5			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000218	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000774	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000233	OMIM:300895	TAS					P	HPO:skoehler[2013-06-06]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000431	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000750	PMID:23395478	PCS		5/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0002650	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000276	PMID:23395478	PCS		1/5			P	HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0005280	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000508	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000028	PMID:23395478	PCS		3/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:300895	Ohdo syndrome, X-linked		HP:0000347	PMID:23395478	PCS		5/5			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-12-05]
OMIM:182190	Sinus node disease and myopia		HP:0011704	OMIM:182190	TAS					P	HPO:probinson[2012-07-22]
OMIM:182190	Sinus node disease and myopia		HP:0011702	OMIM:182190	TAS					P	HPO:probinson[2012-07-22]
OMIM:182190	Sinus node disease and myopia		HP:0011003	OMIM:182190	TAS					P	HPO:probinson[2009-02-17]
OMIM:182190	Sinus node disease and myopia		HP:0000006	OMIM:182190	TAS					I	HPO:probinson[2009-02-17]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0012275	PMID:16301218	PCS					I	HPO:probinson[2013-04-07]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0002510	PMID:16301218	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2020-12-13]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0002059	PMID:16301218	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2020-12-13]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0003577	PMID:16301218	PCS					C	HPO:probinson[2020-12-13]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0000639	PMID:16301218	PCS					P	HPO:probinson[2020-12-13]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0001252	PMID:16301218	PCS	HP:0003577				P	HPO:probinson[2013-04-07];HPO:probinson[2020-12-13]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0100021	PMID:16301218	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-12-13]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0002119	PMID:16301218	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2020-12-13]
OMIM:612900	Cerebral palsy, spastic quadriplegic, 2		HP:0001249	PMID:16301218	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2020-12-13]
OMIM:303350	MASA syndrome		HP:0000252	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0000486	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0001762	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0001761	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0004322	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0002362	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0001274	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0002061	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0002381	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0001181	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0001419	OMIM:303350	IEA					I	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0002808	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0010550	OMIM:303350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:303350	MASA syndrome		HP:0000238	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0002119	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0003307	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0001258	OMIM:303350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:303350	MASA syndrome		HP:0000256	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:303350	MASA syndrome		HP:0001249	OMIM:303350	IEA					P	HPO:iea[2009-02-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002223	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000561	OMIM:308205	TAS					P	HPO:probinson[2012-07-15];HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002542	OMIM:308205	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0007759	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000365	OMIM:308205	TAS		HP:0040283			P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0004322	OMIM:308205	TAS					P	HPO:probinson[2009-02-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000122	PMID:19361614	PCS		1/13	MALE		P	HPO:skoehler[2012-10-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001250	OMIM:308205	TAS					P	HPO:probinson[2009-02-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0005254	OMIM:308205	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0100565	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000958	PMID:19361614	PCS		4/15	FEMALE		P	HPO:probinson[2012-07-15];HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001522	PMID:19361614	PCS		1/13	MALE		C	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001249	OMIM:308205	TAS					P	HPO:probinson[2009-02-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000495	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000175	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000252	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000452	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002079	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000491	OMIM:308205	IEA					P	HPO:skoehler[2018-10-08]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001263	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001581	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0100257	PMID:19361614	PCS		4/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0011496	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000968	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001419	PMID:19361614	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002827	OMIM:308205	TAS		HP:0040283			P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0040189	OMIM:308205	TAS					P	HPO:skoehler[2015-10-05]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002308	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001537	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000964	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001019	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001539	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000966	OMIM:308205	TAS					P	HPO:probinson[2009-02-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0003316	PMID:19361614	PCS		2/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0008404	PMID:19361614	PCS		3/13	MALE		P	HPO:probinson[2012-07-15];HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002788	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000047	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000003	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000962	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0003577	OMIM:308205	TAS					C	HPO:skoehler[2012-10-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0003577	PMID:19361614	PCS		13/13	MALE		C	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001596	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2009-02-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000023	PMID:19361614	PCS		3/13	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002164	OMIM:308205	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001270	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0012444	OMIM:308205	TAS					P	HPO:skoehler[2013-11-28]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0033425	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0008392	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0008391	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0008391	PMID:19361614	PCS		2/15	FEMALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0031291	PMID:19361614	PCS		10/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0500262	PMID:19361614	PCS		12/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0033195	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000613	PMID:19361614	PCS		10/13	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002119	OMIM:308205	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0007502	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001562	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000110	OMIM:308205	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002650	OMIM:308205	TAS					P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001162	OMIM:308205	TAS		HP:0040283			P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002251	OMIM:308205	TAS		2/13	MALE		P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0003819	PMID:19361614	PCS		2/13	MALE		C	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000508	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000822	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0002209	PMID:19361614	PCS		2/15	FEMALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0003811	PMID:19361614	PCS		2/13	MALE		C	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001631	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0001510	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000028	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2012-07-15]
OMIM:308205	IFAP syndrome with or without BRESHECK syndrome		HP:0000104	PMID:19361614	PCS		1/13	MALE		P	HPO:probinson[2023-01-25]
OMIM:619855	Thyroid hormone metabolism, abnormal, 2		HP:0003124	PMID:32718224	PCS		1/5			P	HPO:probinson[2022-06-26]
OMIM:619855	Thyroid hormone metabolism, abnormal, 2		HP:0034289	PMID:32718224	PCS		8/8			P	HPO:probinson[2022-09-05]
OMIM:619855	Thyroid hormone metabolism, abnormal, 2		HP:0034288	PMID:32718224	PCS		8/8			P	HPO:probinson[2022-09-05]
OMIM:619855	Thyroid hormone metabolism, abnormal, 2		HP:0000006	PMID:32718224	PCS					I	HPO:probinson[2022-06-26]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0003577	PMID:17668385	PCS		2/3			C	HPO:probinson[2022-04-18]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0000750	PMID:17668385	PCS		1/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0000276	PMID:17668385	PCS		3/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0001252	PMID:17668385	PCS		2/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0003593	PMID:17668385	PCS		1/3			C	HPO:probinson[2022-04-18]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0001419	PMID:17668385	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0011220	PMID:17668385	PCS		1/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0000378	PMID:17668385	PCS		2/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0000400	PMID:17668385	PCS		8/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0002007	PMID:17668385	PCS		2/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0000256	PMID:17668385;PMID:19377476	PCS		4/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0001763	PMID:17668385	PCS		1/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0000028	PMID:17668385	PCS		2/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-09-25]
OMIM:300659	Intellectual developmental disorder, X-linked 93		HP:0001249	PMID:19377476	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000563	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0010648	PMID:26029576;PMID:29216800	PCS		3/3			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0004322	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0025420	PMID:22940417	PCS		1/1			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0100645	OMIM:130050	IEA					P	HPO:skoehler[2019-09-07]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0012151	PMID:20707836;PMID:11843319	PCS		3/4			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0002619	PMID:29381997	PCS					P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0025019	PMID:10706896	PCS					P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000993	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0001842	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0005620	PMID:22940417;PMID:29216800	PCS		2/2			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0001382	PMID:22940417	PCS		1/1			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0005267	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0031157	PMID:24922459	PCS		27/638			P	HP:probinson[2019-01-22]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0012499	PMID:20707836	PCS		1/3			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0032446	PMID:26029576;PMID:29216800	PCS		2/3			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0032447	PMID:20500229	PCS		2/9			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0009771	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000767	PMID:4023980	PCS		1/4			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0002108	PMID:29381997	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0002107	PMID:22940417;PMID:32471395	PCS		2/2			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000006	PMID:26029576	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0002105	PMID:22940417;PMID:4023980;PMID:26029576;PMID:32471395;PMID:29216800;PMID:11843319	PCS		6/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-26];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000387	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000023	OMIM:130050;PMID:29216800	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0001030	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0001073	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0031364	PMID:26029576	PCS					P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0006094	PMID:26029576	PCS		2/2			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0001903	PMID:11843319	PCS		1/1			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000418	PMID:17640391	PCS					P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0006099	PMID:22940417;PMID:32471395;PMID:29216800	PCS		3/3			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000139	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000978	PMID:26029576;PMID:29216800	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-01-26];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0100749	PMID:26029576	PCS		1/2			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0004933	PMID:22940417	PCS		1/1			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000974	PMID:22940417;PMID:32471395	PCS		2/2			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0006535	PMID:20500229	PCS					P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0025395	PMID:29381997	PCS		1/1			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0001762	PMID:17640391	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000233	PMID:17640391	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0002097	PMID:20500229	PCS		8/9			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0002293	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0025392	PMID:32471395	PCS		1/1			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0030009	OMIM:130050	IEA					P	HPO:skoehler[2019-02-22]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0006480	OMIM:130050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000704	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0100718	PMID:10706896	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0006201	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0006522	PMID:4023980;PMID:32471395	PCS		2/5			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0004944	OMIM:130050	IEA					P	HPO:iea[2009-02-17]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0000028	PMID:29381997	PCS		1/1			P	HPO:probinson[2021-01-26]
OMIM:130050	Ehlers-Danlos syndrome, Vascular type		HP:0001634	PMID:17640391	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-01-26]
OMIM:194080	Denys-Drash syndrome		HP:0000286	PMID:7645607	PCS		1/1			P	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0003774	OMIM:194080	TAS					P	HPO:probinson[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0000100	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0000260	PMID:7645607	PCS		1/1			P	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0000061	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0001153	PMID:7645607	PCS		1/1			P	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0001967	OMIM:194080	TAS					P	HPO:probinson[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0000037	PMID:7645607	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0000776	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0003248	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0000033	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0000112	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0000133	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0001442	OMIM:194080	IEA					I	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0003762	PMID:7645607	PCS		1/1			P	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0000097	PMID:7645607	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0010459	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0025193	PMID:7645607	PCS		1/1			P	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0034198	PMID:7645607	PCS		1/1			C	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0000822	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0003811	PMID:7645607	PCS		1/1			C	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0002667	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:194080	Denys-Drash syndrome		HP:0000006	PMID:1655284	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0000105	PMID:7645607	PCS		1/1			P	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0002643	PMID:7645607	PCS		1/1			P	HPO:probinson[2022-12-17]
OMIM:194080	Denys-Drash syndrome		HP:0000149	OMIM:194080	IEA					P	HPO:iea[2009-02-17]
OMIM:615909	Diamond-Blackfan anemia 13		HP:0011463	PMID:24829207	PCS		5/6			C	HPO:probinson[2015-01-31];HPO:probinson[2022-10-10]
OMIM:615909	Diamond-Blackfan anemia 13		HP:0003829	OMIM:615909	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615909	Diamond-Blackfan anemia 13		HP:0003593	PMID:24829207	PCS		1/6			C	HPO:probinson[2022-10-10]
OMIM:615909	Diamond-Blackfan anemia 13		HP:0001999	PMID:24829207	PCS		0/6			P	HPO:probinson[2015-01-31];HPO:probinson[2022-10-10]
OMIM:615909	Diamond-Blackfan anemia 13		HP:0030270	PMID:24829207	PCS					P	HPO:probinson[2015-01-31];HPO:probinson[2022-10-10]
OMIM:615909	Diamond-Blackfan anemia 13		HP:0000006	PMID:24829207	PCS					I	HPO:probinson[2015-01-31];HPO:probinson[2022-10-10]
OMIM:615909	Diamond-Blackfan anemia 13		HP:0001897	PMID:24829207	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-10]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0003577	PMID:23995685;PMID:27761245	PCS		2/2			C	HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000252	OMIM:604804	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000340	PMID:27761245	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0004322	PMID:23995685	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0002472	OMIM:604804	IEA					P	HPO:iea[2009-02-17]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0001263	PMID:23995685	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000407	PMID:27761245	PCS		0/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0011451	PMID:23995685;PMID:27761245	PCS		2/2			P	HPO:probinson[2022-09-12];HPO:probinson[2022-09-12];HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000448	PMID:27761245	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000007	PMID:15793586	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0001338	PMID:23995685	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0001510	PMID:23995685	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000520	PMID:23995685	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000410	PMID:23995685	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0009879	PMID:23995685	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-12]
OMIM:604804	Microcephaly 3, primary, autosomal recessive		HP:0000687	PMID:23995685	PCS		1/1			P	HPO:probinson[2022-09-12]
OMIM:615896	Hypotrichosis 13		HP:0002224	PMID:22592156	PCS		3/3			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-05-08]
OMIM:615896	Hypotrichosis 13		HP:0003577	PMID:22592156	PCS		3/3			C	HPO:probinson[2022-05-08]
OMIM:615896	Hypotrichosis 13		HP:0006482	PMID:22592156	PCS		0/3			P	HPO:probinson[2022-05-08]
OMIM:615896	Hypotrichosis 13		HP:0011121	PMID:22592156	PCS		0/3			P	HPO:probinson[2022-05-08]
OMIM:615896	Hypotrichosis 13		HP:0000653	PMID:22592156	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:615896	Hypotrichosis 13		HP:0000971	PMID:22592156	PCS		0/3			P	HPO:probinson[2022-05-08]
OMIM:615896	Hypotrichosis 13		HP:0008070	PMID:22592156	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-05-08]
OMIM:615896	Hypotrichosis 13		HP:0000006	PMID:22592156	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0001297	PMID:16444274	PCS		3/20			P	HPO:skoehler[2013-04-18];HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0004970	PMID:17666408	PCS		5/11			P	HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0012727	PMID:16444274	PCS		5/16			P	HPO:probinson[2021-05-02]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0005162	OMIM:132900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0012499	PMID:16444274	PCS		2/16			P	HPO:probinson[2021-05-02]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0033505	PMID:17666408	PCS		1/10			P	HPO:probinson[2021-05-02]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0012495	PMID:32081817	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0100546	PMID:32081817	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0008034	OMIM:132900	TAS					P	HPO:probinson[2012-07-25]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0012493	PMID:32081817	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0012494	PMID:32081817	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0001647	OMIM:132900	TAS					P	HPO:skoehler[2010-06-20]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0012180	PMID:17666408	PCS		2/2			P	HPO:probinson[2013-02-24];HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0002647	PMID:32081817	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0001659	OMIM:132900	TAS					P	HPO:skoehler[2013-04-18]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0001643	PMID:16444274;PMID:32081817;PMID:17666408	PCS		7/28			P	HPO:probinson[2021-02-14];HPO:skoehler[2013-04-18];HPO:probinson[2021-02-14];HPO:probinson[2021-05-02]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0004933	PMID:17666408	PCS		3/10			P	HPO:probinson[2017-12-17];HPO:probinson[2021-05-02]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0000006	PMID:16444274	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-02-14]
OMIM:132900	Aortic aneurysm, familial thoracic 4		HP:0001677	PMID:17666408	PCS		2/7			P	HPO:probinson[2017-12-17]
OMIM:165680	Ossicular malformations, familial		HP:0008591	OMIM:165680	IEA					P	HPO:iea[2009-02-17]
OMIM:165680	Ossicular malformations, familial		HP:0004452	OMIM:165680	IEA					P	HPO:iea[2009-02-17]
OMIM:165680	Ossicular malformations, familial		HP:0000006	OMIM:165680	IEA					I	HPO:iea[2009-02-17]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0008936	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0001320	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000175	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0002389	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0030666	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000750	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0001047	PMID:30976112	PCS		2/2			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000365	PMID:30976112	PCS		2/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000486	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0031936	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0001263	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0001290	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0011800	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0010535	PMID:30976112	PCS		2/2			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000007	PMID:30976112	PCS					I	HPO:probinson[2020-12-04];HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0001338	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0002119	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0001511	PMID:30976112	PCS	HP:0003577	3/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000322	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000347	PMID:30976112	PCS		1/3			P	HPO:probinson[2020-12-04]
OMIM:619074	Cleft palate, proliferative retinopathy, and developmental delay		HP:0000545	PMID:30976112	PCS		3/3			P	HPO:probinson[2020-12-04]
OMIM:193670	Whim syndrome		HP:0000055	OMIM:193670	IEA					P	HPO:skoehler[2009-02-17]
OMIM:193670	Whim syndrome		HP:0004313	PMID:25662009	PCS					P	HPO:probinson[2017-06-14]
OMIM:193670	Whim syndrome		HP:0002110	PMID:25662009	PCS					P	HPO:probinson[2017-06-14]
OMIM:193670	Whim syndrome		HP:0003593	OMIM:193670	IEA					C	HPO:iea[2009-02-17]
OMIM:193670	Whim syndrome		HP:0005561	OMIM:193670	IEA					P	HPO:skoehler[2009-02-17]
OMIM:193670	Whim syndrome		HP:0031160	OMIM:193670	TAS					P	HPO:skoehler[2017-07-13]
OMIM:193670	Whim syndrome		HP:0031020	OMIM:193670	TAS					P	HPO:skoehler[2017-07-13]
OMIM:193670	Whim syndrome		HP:0002718	PMID:25662009	PCS					P	HPO:probinson[2017-06-14]
OMIM:193670	Whim syndrome		HP:0000008	OMIM:193670	IEA					P	HPO:skoehler[2009-02-17]
OMIM:193670	Whim syndrome		HP:0002788	OMIM:193670	IEA					P	HPO:iea[2009-02-17]
OMIM:193670	Whim syndrome		HP:0200043	PMID:25662009	PCS					P	HPO:skoehler[2009-02-17]
OMIM:193670	Whim syndrome		HP:0000006	OMIM:193670	IEA					I	HPO:iea[2009-02-17]
OMIM:193670	Whim syndrome		HP:0001875	PMID:25662009	PCS					P	HPO:iea[2009-02-17]
OMIM:193670	Whim syndrome		HP:0004315	OMIM:193670	IEA					P	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0001265	OMIM:147421	IEA					P	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0002015	OMIM:147421	TAS					P	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0002460	OMIM:147421	TAS					P	HPO:skoehler[2015-12-30]
OMIM:147421	Inclusion body myositis		HP:0003805	OMIM:147421	TAS					P	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0003745	OMIM:147421	TAS					I	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0003701	OMIM:147421	TAS					P	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0000006	OMIM:147421	IEA					I	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0003677	OMIM:147421	TAS					C	HPO:iea[2009-02-17]
OMIM:147421	Inclusion body myositis		HP:0009071	OMIM:147421	TAS					P	HPO:iea[2009-02-17]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000286	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000561	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0003577	PMID:16501574;PMID:16630169	PCS		6/6			C	HPO:probinson[2023-06-10];HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000670	PMID:16501574	PCS		4/4			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0007925	PMID:16501574;PMID:16630169	PCS		8/9			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000365	PMID:16630169	PCS		0/3			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0011968	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0001092	PMID:16501574;PMID:16630169	PCS		7/7			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0008551	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0006297	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000217	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0009944	PMID:16501574	PCS		4/4			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000565	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000378	PMID:16501574;PMID:16630169	PCS		4/7			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0009778	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000006	PMID:16501574	PCS					I	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000687	PMID:16630169	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:620193	Lacrimoauriculodentodigital syndrome-3		HP:0000522	PMID:16501574	PCS		4/4			P	HPO:probinson[2023-06-10]
OMIM:619712	Spermatogenic failure 65		HP:0033393	PMID:34932939	PCS		6/6			P	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0034011	PMID:34932939	PCS		8/8			P	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0032560	PMID:34932939	PCS		5/6			P	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0003251	PMID:34932939	PCS		8/8			P	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0011462	PMID:34932939	PCS		8/8			C	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0000007	PMID:34932939	PCS					I	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0012207	PMID:34932939	PCS		8/8			P	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0012867	PMID:34932939	PCS		6/6			P	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0032558	PMID:34932939	PCS		6/6			P	HPO:probinson[2022-02-24];HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0000798	PMID:34932939	PCS		3/8			P	HPO:probinson[2022-02-24]
OMIM:619712	Spermatogenic failure 65		HP:0032559	PMID:34932939	PCS		6/6			P	HPO:probinson[2022-02-24]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0003621	PMID:25865495	PCS		1/10			C	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0002650	PMID:25865495	PCS		1/10			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0002188	PMID:25865495	PCS		1/10			P	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0025097	PMID:25865495	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0002121	PMID:25865495	PCS		8/9			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0010819	PMID:25865495	PCS		5/8			P	HPO:probinson[2023-01-18];HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0001263	PMID:25865495	PCS		8/9			P	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0001252	PMID:25865495	PCS		1/10			P	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0001251	PMID:25865495	PCS		1/10			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0032794	PMID:25865495	PCS		2/9			P	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0011463	PMID:25865495	PCS		9/10			C	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0000729	PMID:25865495	PCS		7/10			P	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0011170	PMID:25865495	PCS		8/8			P	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0007018	PMID:25865495	PCS		2/10			P	HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0001337	PMID:25865495	PCS		2/10			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0000006	PMID:25865495	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-18]
OMIM:616421	Myoclonic-atonic epilepsy		HP:0001249	PMID:25865495	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-18]
DECIPHER:54	Angelman syndrome (Type 2)		HP:0000252	DECIPHER:54	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:54	Angelman syndrome (Type 2)		HP:0002353	DECIPHER:54	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:54	Angelman syndrome (Type 2)		HP:0002078	DECIPHER:54	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:54	Angelman syndrome (Type 2)		HP:0001250	DECIPHER:54	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:54	Angelman syndrome (Type 2)		HP:0001249	DECIPHER:54	IEA					P	HPO:skoehler[2013-05-29]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0005216	PMID:20598281	PCS		2/3			P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0003676	PMID:20598281	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000486	PMID:20598281	PCS		2/3			P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001271	PMID:20598281	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001252	PMID:20598281	PCS		2/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0012707	PMID:20598281	PCS		1/3			P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001251	OMIM:613559;PMID:20598281	PCS		11/13			P	HPO:probinson[2022-10-06];HPO:skoehler[2012-10-17]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000639	PMID:20598281	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001508	PMID:20598281	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0011463	PMID:20598281	PCS		3/3			C	HPO:probinson[2022-10-06];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001349	PMID:20598281	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0002936	PMID:20598281	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001324	PMID:20598281	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0003202	PMID:20598281	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0007209	PMID:20598281	PCS		2/3			P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0002015	PMID:20598281	PCS		1/3			P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0002376	PMID:20598281	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001260	PMID:20598281	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0011925	PMID:20598281	PCS					P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001263	PMID:20598281	PCS		3/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0002151	PMID:20598281	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0001284	OMIM:613559;PMID:20598281	PCS		12/13			P	HPO:probinson[2022-10-06];HPO:skoehler[2012-10-17]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0002590	PMID:20598281	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0011923	PMID:20598281	PCS					P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000508	PMID:20598281	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000602	PMID:20598281	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000007	PMID:20598281	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000505	PMID:20598281	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000648	PMID:20598281	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0008347	PMID:20598281	PCS					P	HPO:probinson[2022-10-06]
OMIM:613559	Combined oxidative phosphorylation deficiency 7		HP:0000544	PMID:20598281	PCS		2/3			P	HPO:probinson[2022-10-06]
OMIM:602440	Amyotrophy, monomelic		HP:0003587	OMIM:602440	IEA					C	HPO:iea[2009-02-17]
OMIM:602440	Amyotrophy, monomelic		HP:0007181	OMIM:602440	TAS					P	HPO:probinson[2009-02-17]
OMIM:602440	Amyotrophy, monomelic		HP:0003445	OMIM:602440	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602440	Amyotrophy, monomelic		HP:0003484	OMIM:602440	TAS					P	HPO:probinson[2012-07-17]
OMIM:602440	Amyotrophy, monomelic		HP:0031372	OMIM:602440	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602440	Amyotrophy, monomelic		HP:0002380	OMIM:602440	IEA					P	HPO:iea[2009-02-17]
OMIM:602440	Amyotrophy, monomelic		HP:0010873	OMIM:602440	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602440	Amyotrophy, monomelic		HP:0003745	OMIM:602440	IEA					I	HPO:iea[2009-02-17]
OMIM:612653	Spherocytosis, type 4		HP:0005502	PMID:8471774	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2023-02-24]
OMIM:612653	Spherocytosis, type 4		HP:0004444	PMID:8471774	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2023-02-24]
OMIM:612653	Spherocytosis, type 4		HP:0002904	OMIM:612653	TAS					P	HPO:skoehler[2015-12-30]
OMIM:612653	Spherocytosis, type 4		HP:0011462	PMID:8471774	PCS		1/1			C	HPO:probinson[2023-02-24]
OMIM:612653	Spherocytosis, type 4		HP:0001878	PMID:8471774	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2023-02-24]
OMIM:612653	Spherocytosis, type 4		HP:0001923	PMID:8471774	PCS		1/1			P	HPO:probinson[2013-04-07];HPO:probinson[2023-02-24]
OMIM:612653	Spherocytosis, type 4		HP:0000006	PMID:8471774	PCS					I	HPO:probinson[2013-04-07];HPO:probinson[2023-02-24]
OMIM:612653	Spherocytosis, type 4		HP:0000952	OMIM:612653	TAS					P	HPO:skoehler[2015-12-30]
OMIM:612653	Spherocytosis, type 4		HP:0001744	PMID:8471774	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-24]
OMIM:614222	Warburg micro syndrome 3		HP:0002069	PMID:21473985	PCS		3/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0003577	PMID:21473985	PCS		12/12			C	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000046	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0000189	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0002540	PMID:21473985	PCS		11/11			P	HPO:probinson[2022-11-21];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0001371	OMIM:614222	TAS					P	HPO:probinson[2013-08-10]
OMIM:614222	Warburg micro syndrome 3		HP:0002120	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0003199	OMIM:614222	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614222	Warburg micro syndrome 3		HP:0003196	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0000482	PMID:21473985	PCS		12/12			P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000064	PMID:21473985	PCS		1/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000581	OMIM:614222	TAS				HP:0012825	P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0032794	PMID:21473985	PCS		1/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0002061	PMID:21473985	PCS		6/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0002280	PMID:21473985	PCS		1/7			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000639	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0000518	PMID:21473985	PCS	HP:0003577	12/12			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000616	PMID:21473985	PCS		12/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0100704	PMID:21473985	PCS		8/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000519	OMIM:614222	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614222	Warburg micro syndrome 3		HP:0000998	OMIM:614222	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614222	Warburg micro syndrome 3		HP:0002119	PMID:21473985	PCS		3/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0008897	PMID:21473985	PCS		12/12			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0002714	OMIM:614222	TAS					P	HPO:probinson[2013-08-10]
OMIM:614222	Warburg micro syndrome 3		HP:0006610	OMIM:614222	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614222	Warburg micro syndrome 3		HP:0008734	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0000594	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0002751	OMIM:614222	TAS					P	HPO:probinson[2013-08-10]
OMIM:614222	Warburg micro syndrome 3		HP:0008936	PMID:21473985	PCS		12/12			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0002476	PMID:21473985	PCS		1/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0002510	PMID:21473985	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000054	PMID:21473985	PCS		2/4			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000252	OMIM:614222	TAS					P	HPO:probinson[2013-08-10]
OMIM:614222	Warburg micro syndrome 3		HP:0001344	PMID:21473985	PCS		2/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0002079	PMID:21473985	PCS		6/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0001263	PMID:21473985	PCS		12/12			P	HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0005484	PMID:21473985	PCS		12/12			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000294	OMIM:614222	TAS					P	HPO:probinson[2013-08-10]
OMIM:614222	Warburg micro syndrome 3		HP:0011448	PMID:21473985	PCS		1/12			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000568	PMID:21473985	PCS		12/12			P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000007	PMID:21473985	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000648	PMID:21473985	PCS		8/8			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0004209	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0000400	OMIM:614222	TAS					P	HPO:probinson[2013-08-10]
OMIM:614222	Warburg micro syndrome 3		HP:0002126	PMID:21473985	PCS		4/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-21]
OMIM:614222	Warburg micro syndrome 3		HP:0000347	OMIM:614222	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614222	Warburg micro syndrome 3		HP:0000248	OMIM:614222	TAS					P	HPO:probinson[2013-08-10]
OMIM:600257	Bor-Duane hydrocephalus contiguous gene syndrome		HP:0034342	PMID:7849713	PCS					P	HPO:probinson[2022-09-05]
OMIM:600257	Bor-Duane hydrocephalus contiguous gene syndrome		HP:0000238	PMID:7849713	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:600257	Bor-Duane hydrocephalus contiguous gene syndrome		HP:0000598	PMID:7849713	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:600257	Bor-Duane hydrocephalus contiguous gene syndrome		HP:0001466	PMID:7849713	PCS					I	HPO:probinson[2022-09-04]
OMIM:600257	Bor-Duane hydrocephalus contiguous gene syndrome		HP:0009921	PMID:7849713	PCS					P	HPO:probinson[2022-09-04]
OMIM:600257	Bor-Duane hydrocephalus contiguous gene syndrome		HP:0000006	PMID:7849713	PCS					I	HPO:probinson[2022-09-04]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0003621	PMID:30929741	PCS		18/28			C	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0000640	PMID:30929741	PCS		7/30			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0002067	PMID:30929741	PCS		0/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0003487	PMID:30929741	PCS		29/30			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0001288	PMID:30929741	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0000012	PMID:30929741	PCS		11/30			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0001332	PMID:30929741	PCS		0/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0001761	PMID:30929741	PCS		1/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0002395	PMID:30929741	PCS		30/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0001260	PMID:30929741	PCS		1/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0002061	PMID:30929741	PCS		29/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0002070	PMID:30929741	PCS		7/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0007350	PMID:30929741	PCS		26/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0011463	PMID:30929741	PCS		10/28			C	HPO:probinson[2022-03-28];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0000605	PMID:30929741	PCS		0/30			P	HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0001258	PMID:30929741	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0000641	PMID:30929741	PCS		7/30			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0001268	PMID:30929741	PCS		7/30			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0000006	PMID:30929741	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-28]
OMIM:618418	Spastic paraplegia 80, autosomal dominant		HP:0006986	PMID:30929741	PCS		1/30			P	HPO:probinson[2022-03-28]
OMIM:616435	Fanconi anemia, complementation group T		HP:0010628	PMID:26046368	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0003577	PMID:26046368	PCS		2/2			C	HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0000365	PMID:26046368	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0004322	PMID:26046368	PCS		1/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0003221	PMID:26046368	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0001903	PMID:26046368	PCS		2/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0004808	PMID:26046368	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0000007	PMID:26046368	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0009942	PMID:26046368	PCS		1/2			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0005528	OMIM:616435	TAS					P	HPO:skoehler[2015-07-05]
OMIM:616435	Fanconi anemia, complementation group T		HP:0009778	PMID:26046368	PCS		1/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0001873	PMID:26046368	PCS		2/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-11]
OMIM:616435	Fanconi anemia, complementation group T		HP:0001876	PMID:26046368	PCS		1/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-11]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002421	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0011917	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0004325	PMID:31290619	PCS		2/2			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002521	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0004322	PMID:31290619;PMID:28766551	PCS		3/3			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0001272	PMID:31290619	PCS		2/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0001290	PMID:31290619	PCS		2/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0033503	PMID:31290619	PCS		1/1			P	HPO:probinson[2021-02-13]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0008093	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0007083	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0001508	PMID:28766551	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0001885	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002059	PMID:31290619	PCS		2/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0005643	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002750	PMID:28766551	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002376	PMID:31290619	PCS	HP:0003593	2/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0003221	PMID:28766551	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002151	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002490	PMID:31290619	PCS		1/1			P	HPO:probinson[2021-02-13]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0011097	PMID:31290619	PCS	HP:0011463	2/2			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0000426	PMID:28766551	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0000007	PMID:28766551	PCS					I	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0008347	PMID:31290619	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0009237	PMID:28766551	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0002007	PMID:28766551	PCS		1/1			P	HPO:probinson[2020-12-07]
OMIM:619060	Mitochondrial complex IV deficiency, nuclear type 16		HP:0001336	PMID:31290619	PCS		1/2			P	HPO:probinson[2020-12-07]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0009926	PMID:25893599	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0001000	PMID:25893599	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0000670	PMID:25893599	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0000252	PMID:25893599	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0001596	PMID:25893599	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0001321	PMID:25893599	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0001263	PMID:25893599	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0001251	PMID:25893599	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0003593	OMIM:616353	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0031413	PMID:25893599	PCS		3/3			P	HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0008070	PMID:25893599	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0006480	PMID:25893599	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0001508	PMID:25893599	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0000007	PMID:25893599	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0001511	PMID:25893599	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0008404	PMID:25893599	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0005528	PMID:25893599	PCS		4/4			P	HPO:probinson[2022-09-26]
OMIM:616353	Dyskeratosis congenita, autosomal recessive 6		HP:0002745	PMID:25893599	PCS		3/4			P	HPO:probinson[2022-09-26]
OMIM:609273	Nemaline myopathy 6		HP:0003202	PMID:21109227	PCS					P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0010628	PMID:11731279	PCS		0/24			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-14]
OMIM:609273	Nemaline myopathy 6		HP:0003236	PMID:21109227	PCS		0/42			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06];HPO:probinson[2024-03-14]
OMIM:609273	Nemaline myopathy 6		HP:0003552	OMIM:609273	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609273	Nemaline myopathy 6		HP:0001288	PMID:21109227	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0003198	PMID:21109227	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0003551	PMID:21109227	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0003690	PMID:21109227	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0011463	PMID:21109227	PCS		42/42			C	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06];HPO:probinson[2024-03-14]
OMIM:609273	Nemaline myopathy 6		HP:0009046	PMID:21109227	PCS					P	HPO:skoehler[2012-11-22];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0000006	PMID:21109227	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0003798	PMID:21109227	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0003677	PMID:21109227	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0003546	PMID:21109227	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:609273	Nemaline myopathy 6		HP:0003722	PMID:21109227	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:604757	Craniosynostosis 2		HP:0001199	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:604757	Craniosynostosis 2		HP:0001363	PMID:23949913	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0001156	PMID:23949913	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0000540	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:604757	Craniosynostosis 2		HP:0000243	PMID:23949913	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0001123	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:604757	Craniosynostosis 2		HP:0001250	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:604757	Craniosynostosis 2		HP:0000185	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:604757	Craniosynostosis 2		HP:0000262	PMID:23949913	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0003593	PMID:23949913	PCS					C	HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0011069	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:604757	Craniosynostosis 2		HP:0011318	PMID:23949913	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0011315	PMID:23949913	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0011330	PMID:23949913	PCS		1/8			P	HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0000601	PMID:23949913	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0002007	PMID:23949913	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0002315	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:604757	Craniosynostosis 2		HP:0002645	PMID:23949913	PCS		1/8			P	HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0000006	PMID:8106171	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0000248	PMID:23949913	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0001249	PMID:23949913	PCS		0/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:604757	Craniosynostosis 2		HP:0000545	OMIM:604757	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0008936	PMID:11013136	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001397	PMID:11013136	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0031956	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001662	PMID:11013136	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0002151	PMID:19295170;PMID:11013136	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0002240	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001290	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0012444	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0031964	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001508	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0000007	PMID:11013136	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001943	PMID:11013136	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001712	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0008872	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001635	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001714	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001511	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0008315	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0033092	PMID:11013136	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0002104	PMID:11013136	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0001942	PMID:11013136	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619048	Mitochondrial complex IV deficiency, nuclear type 4		HP:0003348	PMID:19295170	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001254	PMID:26486472	PCS		1/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0008936	PMID:26486472	PCS		2/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0002521	PMID:26486472	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0003577	PMID:26486472	PCS		2/3			C	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001266	PMID:26486472	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001250	PMID:26486472	PCS				HP:0031375	P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0011968	PMID:26486472	PCS		1/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0002120	PMID:26486472	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001285	PMID:26486472	PCS		1/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001252	PMID:26486472	PCS		3/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0012736	PMID:26486472	PCS		3/3			P	HPO:probinson[2022-09-27];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0033258	PMID:26486472	PCS		1/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0033363	PMID:26486472	PCS		2/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001518	PMID:26486472	PCS		2/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0000817	PMID:26486472	PCS		1/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0000007	PMID:26486472	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0200134	PMID:26486472	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001511	PMID:26486472	PCS		1/3			P	HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001257	PMID:26486472	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0001336	PMID:26486472	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:617065	Epileptic encephalopathy, early infantile, 40		HP:0003623	PMID:26486472	PCS		1/3			C	HPO:probinson[2022-09-27]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001276	PMID:28940097	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0004886	PMID:28940097	PCS	HP:0003577	1/1			P	HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001310	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001272	OMIM:618356	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001250	OMIM:618356	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001252	PMID:28940097	PCS		1/1			P	HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001251	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000162	PMID:28940097	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0002080	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001508	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000718	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000739	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000316	PMID:28940097	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000878	PMID:28940097	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000237	PMID:28940097	PCS		1/1			P	HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001347	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0003623	PMID:28940097	PCS		1/1			C	HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001265	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000175	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001187	PMID:28940097	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000252	OMIM:618356	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000431	PMID:28940097	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0003487	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0031936	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0011968	OMIM:618356	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001260	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001263	PMID:28940097	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0002075	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0002093	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000426	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000007	PMID:28940097	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001558	OMIM:618356	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0002205	PMID:28940097	PCS		1/1			P	HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000762	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0002643	PMID:28940097	PCS	HP:0003623	1/1			P	HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0000347	PMID:28940097	PCS		1/1			P	HPO:probinson[2023-01-20]
OMIM:618356	Neurodevelopmental disorder with central and peripheral motor dysfunction		HP:0001336	OMIM:618356	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603010	Deafness, autosomal recessive 17		HP:0000407	OMIM:603010	TAS					P	HPO:skoehler[2015-12-30]
OMIM:603010	Deafness, autosomal recessive 17		HP:0000007	OMIM:603010	TAS					I	HPO:skoehler[2015-12-30]
OMIM:277200	Right ventricular hypoplasia, isolated		HP:0004762	OMIM:277200	IEA					P	HPO:iea[2009-02-17]
OMIM:277200	Right ventricular hypoplasia, isolated		HP:0000007	OMIM:277200	IEA					I	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000692	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0002213	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0030863	OMIM:268320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:268320	Rodrigues blindness		HP:0004322	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000482	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0008070	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000968	OMIM:268320	IEA					P	HPO:skoehler[2015-01-14]
OMIM:268320	Rodrigues blindness		HP:0000618	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0001999	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000007	OMIM:268320	IEA					I	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000568	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000647	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000411	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0000446	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:268320	Rodrigues blindness		HP:0001249	OMIM:268320	IEA					P	HPO:iea[2009-02-17]
OMIM:104530	Amelogenesis imperfecta, type IA		HP:0000705	PMID:23958762	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-16]
OMIM:104530	Amelogenesis imperfecta, type IA		HP:0006297	PMID:23958762	PCS		2/2			P	HPO:probinson[2023-03-16]
OMIM:104530	Amelogenesis imperfecta, type IA		HP:0000679	PMID:23958762	PCS		1/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-16]
OMIM:104530	Amelogenesis imperfecta, type IA		HP:0006311	OMIM:104530	IEA					P	HPO:iea[2009-02-17]
OMIM:104530	Amelogenesis imperfecta, type IA		HP:0009722	PMID:23958762	PCS		1/2			P	HPO:probinson[2023-03-16]
OMIM:104530	Amelogenesis imperfecta, type IA		HP:0000006	PMID:23958762	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-16]
OMIM:104530	Amelogenesis imperfecta, type IA		HP:0000951	PMID:23958762	PCS		0/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-03-16]
DECIPHER:68	16p11.2-p12.2 microdeletion syndrome		HP:0000271	DECIPHER:68	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:68	16p11.2-p12.2 microdeletion syndrome		HP:0008872	DECIPHER:68	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:68	16p11.2-p12.2 microdeletion syndrome		HP:0000307	DECIPHER:68	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:68	16p11.2-p12.2 microdeletion syndrome		HP:0001249	DECIPHER:68	IEA					P	HPO:skoehler[2013-05-29]
OMIM:603776	Hypercholesterolemia, familial, 3		HP:0003124	PMID:10205269	PCS		HP:0040280			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-09-20]
OMIM:603776	Hypercholesterolemia, familial, 3		HP:0001084	PMID:10205269	PCS					P	HPO:probinson[2020-09-20]
OMIM:603776	Hypercholesterolemia, familial, 3		HP:0010874	PMID:10205269	PCS					P	HPO:probinson[2020-09-20]
OMIM:603776	Hypercholesterolemia, familial, 3		HP:0001114	PMID:10205269	PCS					P	HPO:probinson[2020-09-20]
OMIM:603776	Hypercholesterolemia, familial, 3		HP:0031886	PMID:10357843	IEA					P	HPO:probinson[2020-09-20]
OMIM:603776	Hypercholesterolemia, familial, 3		HP:0000006	PMID:10205269	PCS		HP:0040280			I	HPO:skoehler[2013-01-14];HPO:probinson[2020-09-20]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000286	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0010804	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000486	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001250	PMID:27436265	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0003196	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001252	PMID:27436265	PCS		2/2			P	HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001251	PMID:27436265	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0003593	PMID:27436265	PCS		2/2			C	HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000718	PMID:27436265	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000752	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0002019	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000358	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0002311	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000098	PMID:27436265	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000771	PMID:27436265	PCS		1/2			P	HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0011968	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000490	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001263	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0011800	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001182	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000729	PMID:27436265	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000722	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0004209	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0005616	PMID:27436265	PCS		1/1			P	HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001852	PMID:27436265	PCS		1/2			P	HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001257	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000006	PMID:25228304	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000248	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000369	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001270	PMID:27436265	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000739	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000414	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000733	PMID:27436265	PCS		1/2			P	HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000219	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0002714	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000256	PMID:27436265	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000750	PMID:27436265	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0002650	PMID:27436265	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0031936	PMID:27436265	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000276	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000194	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0003186	PMID:27436265	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-03]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0005280	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000348	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0002007	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001357	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0000545	OMIM:618430	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618430	Developmental delay with variable intellectual impairment and behavioral abnormalities		HP:0001513	OMIM:618430	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0003015	OMIM:156510	TAS					P	HPO:probinson[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0000233	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0004322	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0004220	OMIM:156510	TAS					P	HPO:probinson[2012-06-09]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0010047	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0100255	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0006480	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0000926	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0000327	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0009577	OMIM:156510	TAS					P	HPO:probinson[2012-06-09]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0000444	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0000322	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0000006	OMIM:156510	IEA					I	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0005625	OMIM:156510	IEA					P	HPO:iea[2009-02-17]
OMIM:156510	Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly		HP:0005877	OMIM:156510	TAS					P	HPO:probinson[2009-02-17]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0003621	PMID:28965846	PCS		5/8			C	HPO:probinson[2022-12-13]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0000365	PMID:28965846	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0000639	PMID:28965846	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0011463	PMID:28965846	PCS		3/8			C	HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0000007	PMID:28965846	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-13]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0000648	PMID:28965846	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0000505	PMID:28965846	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617717	Auditory neuropathy and optic atrophy		HP:0000510	PMID:28965846	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:109000	AURICULOOSTEODYSPLASIA		HP:0001385	OMIM:109000	IEA					P	HPO:iea[2009-02-17]
OMIM:109000	AURICULOOSTEODYSPLASIA		HP:0004322	OMIM:109000	IEA					P	HPO:iea[2009-02-17]
OMIM:109000	AURICULOOSTEODYSPLASIA		HP:0009907	OMIM:109000	TAS					P	HPO:probinson[2013-04-01]
OMIM:109000	AURICULOOSTEODYSPLASIA		HP:0003083	OMIM:109000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:109000	AURICULOOSTEODYSPLASIA		HP:0000006	OMIM:109000	IEA					I	HPO:iea[2009-02-17]
OMIM:609529	Immunoglobulin A deficiency 2		HP:0005425	OMIM:609529	IEA					P	HPO:skoehler[2013-01-09]
OMIM:609529	Immunoglobulin A deficiency 2		HP:0004798	OMIM:609529	IEA					P	HPO:skoehler[2013-01-09]
OMIM:609529	Immunoglobulin A deficiency 2		HP:0002960	OMIM:609529	IEA					P	HPO:skoehler[2013-01-09]
OMIM:609529	Immunoglobulin A deficiency 2		HP:0004332	OMIM:609529	IEA					P	HPO:skoehler[2013-01-09]
OMIM:609529	Immunoglobulin A deficiency 2		HP:0002720	OMIM:609529	IEA					P	HPO:skoehler[2013-01-09]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0002069	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0002311	PMID:23647072	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0002521	PMID:23647072	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0001344	PMID:23647072	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0000750	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0001250	PMID:23647072	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0001263	PMID:23647072;PMID:23033978	PCS		2/2			P	HPO:probinson[2022-08-13];HPO:skoehler[2015-06-22];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0001252	PMID:23647072	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0005484	PMID:23647072	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0003593	PMID:23647072	PCS		1/1			C	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0032794	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0011147	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0011097	PMID:23647072	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0000718	PMID:23033978	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0000729	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0200134	PMID:23647072	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0001319	PMID:23033978	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0002317	PMID:23647072	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0000006	PMID:23033978	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-13]
OMIM:616409	Developmental and epileptic encephalopathy 33		HP:0003623	PMID:23033978	PCS		1/1			C	HPO:probinson[2022-08-13]
OMIM:613571	Disordered steroidogenesis due to cytochrome P450 oxidoreductase		HP:0000062	OMIM:613571	IEA					P	HPO:skoehler[2013-01-09]
OMIM:613571	Disordered steroidogenesis due to cytochrome P450 oxidoreductase		HP:0003154	OMIM:613571	IEA					P	HPO:skoehler[2013-06-02]
OMIM:613571	Disordered steroidogenesis due to cytochrome P450 oxidoreductase		HP:0000007	PMID:18559916	PCS					I	HPO:skoehler[2013-06-02];HPO:probinson[2020-07-21]
OMIM:613571	Disordered steroidogenesis due to cytochrome P450 oxidoreductase		HP:0008258	OMIM:613571	IEA					P	HPO:skoehler[2013-06-02]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002983	OMIM:271665	TAS					P	HPO:skoehler[2012-10-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003311	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0005257	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003396	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0001252	PMID:19110212	PCS		11/20			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003196	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000283	PMID:19110212	PCS		13/20			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0010049	OMIM:271665	TAS					P	HPO:probinson[2012-05-08]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0009381	PMID:20223752	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002979	PMID:19110212;PMID:20223752	PCS		9/22			P	HPO:probinson[2023-02-12];HPO:probinson[2015-02-23];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000316	PMID:19110212;PMID:20223752	PCS		19/22			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0001840	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0001169	PMID:19110212;PMID:20223752	PCS		22/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0005622	PMID:19110212;PMID:20223752	PCS		22/22			P	HPO:probinson[2023-02-12];HPO:probinson[2012-05-08];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003320	PMID:19110212;PMID:20223752	PCS		11/22			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0001263	PMID:19110212;PMID:20223752	PCS		4/22			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0005462	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003085	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0011800	OMIM:271665	TAS					P	HPO:skoehler[2015-11-15]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0006380	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000926	PMID:19110212;PMID:20223752	PCS		22/22			P	HPO:probinson[2023-02-12];HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002869	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000767	PMID:19110212;PMID:20223752	PCS		6/22			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000007	PMID:19110212	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0009931	PMID:19110212;PMID:20223752	PCS		17/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000922	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000768	PMID:20223752	PCS		1/2			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002987	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000520	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002787	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0006009	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003015	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000343	PMID:19110212;PMID:20223752	PCS		16/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0001591	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000260	PMID:19110212	PCS		8/20			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0030674	PMID:20223752	PCS		2/2			C	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0001230	OMIM:271665	TAS					P	HPO:probinson[2012-05-08]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0100593	PMID:19110212;PMID:20223752	PCS		9/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0001270	PMID:19110212;PMID:20223752	PCS		15/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0009164	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0011120	PMID:19110212	PCS		17/20			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0008873	PMID:19110212	PCS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0030043	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000218	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0006532	OMIM:271665	TAS					P	HPO:probinson[2012-05-08]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000774	PMID:19110212;PMID:20223752	PCS		15/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000773	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0009803	PMID:19110212	PCS		8/20			P	HPO:probinson[2012-06-03];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000457	PMID:20223752	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003026	PMID:19110212;PMID:20223752	PCS		22/22			P	HPO:probinson[2023-02-12];HPO:probinson[2012-05-08];HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0003467	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002650	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0004279	PMID:19110212;PMID:20223752	PCS		22/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002651	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002176	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000272	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000470	PMID:19110212;PMID:20223752	PCS		9/22			P	HPO:probinson[2023-02-12]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0005280	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002091	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0010655	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000907	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0009875	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0002007	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0006600	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:271665	Spondylometaepiphyseal dysplasia, short Limb-Hand type		HP:0000347	OMIM:271665	TAS					P	HPO:probinson[2009-02-17]
OMIM:144100	Hyperhidrosis, gustatory		HP:0000975	OMIM:144100	TAS					P	HPO:probinson[2009-02-17]
OMIM:144100	Hyperhidrosis, gustatory		HP:0000006	OMIM:144100	IEA					I	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0003279	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0003577	PMID:35450306	PCS		2/2			C	HPO:probinson[2024-03-08]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000343	PMID:35450306	PCS		2/2			P	HPO:probinson[2012-05-01]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0001773	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0001156	PMID:35450306	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0004322	PMID:35450306	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0010049	OMIM:190351	TAS					P	HPO:probinson[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0008070	PMID:35450306	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0010743	OMIM:190351	TAS					P	HPO:probinson[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0009381	OMIM:190351	TAS				HP:0012828	P	HPO:probinson[2012-06-10]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000319	PMID:35450306	PCS		2/2			P	HPO:probinson[2012-05-01]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000938	OMIM:190351	IEA				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000414	PMID:35450306	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000678	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000219	PMID:35450306	PCS		2/2			P	HPO:skoehler[2013-06-04]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000411	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0001249	PMID:35450306	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0009803	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0005743	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0002213	PMID:35450306	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0002650	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0004279	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0002750	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000430	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0011069	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0010259	OMIM:190351	TAS					P	HPO:probinson[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0002805	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000447	OMIM:190351	IEA					P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000006	PMID:35450306	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0005338	PMID:35450306	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:190351	Trichorhinophalangeal syndrome, type III		HP:0000962	PMID:35450306	PCS		2/2			P	HPO:probinson[2024-12-03]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0001508	PMID:18572020	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-25]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0001518	OMIM:613217	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0002041	PMID:18572020	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-25]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0011473	PMID:18572020	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0003593	PMID:18572020	PCS		3/5			C	HPO:probinson[2023-02-25]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0034588	PMID:18572020	PCS		5/5			P	HPO:probinson[2023-03-31]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0000007	PMID:18572020	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-25]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0001369	OMIM:613217	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613217	Diarrhea 5, with tufting enteropathy, congenital		HP:0003623	PMID:18572020	PCS		2/5			C	HPO:probinson[2023-02-25]
OMIM:612109	Oculoauricular syndrome		HP:0000387	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000541	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000480	PMID:25574057	PCS		1/2			P	HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0003298	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000482	PMID:18423520;PMID:25574057	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0012376	PMID:18423520	PCS		2/3			P	HPO:skoehler[2013-10-22];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000518	PMID:18423520	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000639	PMID:18423520	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000639	PMID:25574057	PCS	HP:0003577	1/2			P	HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0011484	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0032286	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000519	PMID:25574057	PCS	HP:0003577	2/2			P	HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000612	PMID:18423520	PCS		3/3			P	HP:probinson[2021-10-21];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0025514	PMID:18423520	PCS		2/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000579	PMID:25574057	PCS		1/2			P	HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0001104	PMID:18423520	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000510	OMIM:612109	TAS					P	HPO:skoehler[2015-07-26]
OMIM:612109	Oculoauricular syndrome		HP:0007700	PMID:18423520	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0020049	PMID:25574057	PCS		1/2			P	HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000533	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0006934	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0007906	OMIM:612109	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612109	Oculoauricular syndrome		HP:0011523	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000627	PMID:25574057	PCS		2/2			P	HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000007	PMID:18423520	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000568	PMID:18423520	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000667	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000548	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000647	PMID:18423520;PMID:25574057	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-21];HPO:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0003778	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000567	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000666	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000402	PMID:18423520	PCS		1/3			P	HP:probinson[2021-10-21]
OMIM:612109	Oculoauricular syndrome		HP:0000369	PMID:25574057	PCS		2/2			P	HPO:probinson[2021-10-21]
OMIM:189600	TORTICOLLIS		HP:0000473	OMIM:189600	IEA					P	HPO:iea[2009-02-17]
OMIM:189600	TORTICOLLIS		HP:0000006	OMIM:189600	IEA					I	HPO:iea[2009-02-17]
OMIM:189600	TORTICOLLIS		HP:0000324	OMIM:189600	IEA					P	HPO:iea[2009-02-17]
OMIM:140400	Progressive familial heart block, type II		HP:0005178	OMIM:140400	PCS					P	HPO:probinson[2012-04-11]
OMIM:140400	Progressive familial heart block, type II		HP:0001279	OMIM:140400	PCS					P	HPO:probinson[2012-04-11]
OMIM:140400	Progressive familial heart block, type II		HP:0001678	OMIM:140400	PCS					P	HPO:probinson[2012-04-11]
OMIM:140400	Progressive familial heart block, type II		HP:0000006	PMID:16086176	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-07-12]
OMIM:140400	Progressive familial heart block, type II		HP:0001645	OMIM:140400	PCS					P	HPO:probinson[2012-04-11]
OMIM:140400	Progressive familial heart block, type II		HP:0001688	OMIM:140400	PCS					P	HPO:probinson[2012-04-11]
OMIM:140400	Progressive familial heart block, type II		HP:0001699	OMIM:140400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0002069	OMIM:300088	TAS					P	HPO:probinson[2009-02-17]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0006813	PMID:19752159	PCS		2/3			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0002133	OMIM:300088	IEA					P	HPO:iea[2009-02-17]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0002123	OMIM:300088	TAS					P	HPO:probinson[2012-07-20]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0002376	OMIM:300088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0002121	OMIM:300088	TAS					P	HPO:probinson[2012-07-20]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0010819	PMID:19752159	PCS		1/3			P	HPO:probinson[2012-07-20];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0001263	OMIM:300088	TAS		HP:0040282			P	HPO:probinson[2009-02-17]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0003593	OMIM:300088	IEA		1/3			C	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0025190	PMID:19752159	PCS		2/3			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0032810	PMID:19752159	PCS		1/3			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0000709	OMIM:300088	IEA					P	HPO:iea[2009-02-17]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0011463	PMID:19752159	PCS		2/3			C	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0032660	PMID:19752159	PCS		1/3			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0000729	PMID:19752159	PCS		1/3			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0000718	OMIM:300088	IEA					P	HPO:iea[2009-02-17]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0002119	PMID:19752159	PCS		1/3			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0001417	PMID:18469813	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0007359	OMIM:300088	TAS					P	HPO:probinson[2009-02-17]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0007018	PMID:19752159	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:300088	Epileptic encephalopathy, early infantile, 9		HP:0001249	OMIM:300088	IEA		HP:0040282			P	HPO:skoehler[2015-08-05]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0004325	PMID:30526862;PMID:30778726	PCS		4/6			P	HPO:probinson[2022-06-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000286	OMIM:618342	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0004322	PMID:30526862;PMID:30778726	PCS		6/8			P	HPO:probinson[2022-06-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0003394	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0003593	PMID:30778726	PCS		2/3			C	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0001290	OMIM:618342	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000319	PMID:30526862;PMID:30778726	PCS		6/8			P	HPO:probinson[2022-06-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0011463	PMID:30778726	PCS		1/3			C	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000718	PMID:30526862;PMID:30778726	PCS		7/8			P	HPO:probinson[2022-06-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0012471	PMID:30526862	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000678	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0020045	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000752	PMID:30778726	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000278	OMIM:618342	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0001249	PMID:30526862;PMID:30778726	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-19];HPO:probinson[2022-06-19];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0003763	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0002553	PMID:30778726	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000494	OMIM:618342	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000252	PMID:30526862;PMID:30778726	PCS		7/8			P	HPO:probinson[2022-06-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000490	PMID:30778726	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0001263	PMID:30778726	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0011095	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000407	PMID:30778726	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000007	PMID:30526862	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000322	PMID:30778726	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000369	PMID:30778726	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0001337	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000325	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000463	PMID:30778726	PCS		2/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0002240	PMID:30526862	PCS		1/6			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0001270	PMID:30526862	PCS		3/6			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0012444	PMID:30526862	PCS		1/6			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000733	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000736	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0002119	PMID:30526862	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000218	PMID:30778726	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0006335	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000411	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000179	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000750	PMID:30526862;PMID:30778726	PCS		9/9			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000431	OMIM:618342	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0031936	PMID:30778726	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000232	PMID:30526862;PMID:30778726	PCS		5/8			P	HPO:probinson[2022-06-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0002057	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000194	OMIM:618342	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0100876	PMID:30778726	PCS		2/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000668	PMID:30526862	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000307	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0007018	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:618342	Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature		HP:0000347	PMID:30778726	PCS		1/3			P	HPO:probinson[2022-06-19]
OMIM:601820	Hyperinsulinemic hypoglycemia, familial, 2		HP:0001520	OMIM:601820	IEA					P	HPO:iea[2009-02-17]
OMIM:601820	Hyperinsulinemic hypoglycemia, familial, 2		HP:0004510	OMIM:601820	IEA					P	HPO:iea[2009-02-17]
OMIM:601820	Hyperinsulinemic hypoglycemia, familial, 2		HP:0000825	PMID:8923010	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:601820	Hyperinsulinemic hypoglycemia, familial, 2		HP:0034346	PMID:8923010	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:601820	Hyperinsulinemic hypoglycemia, familial, 2		HP:0000007	PMID:8923010	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:601820	Hyperinsulinemic hypoglycemia, familial, 2		HP:0001943	OMIM:601820	IEA					P	HPO:iea[2009-02-17]
OMIM:601820	Hyperinsulinemic hypoglycemia, familial, 2		HP:0003623	PMID:8923010	PCS		1/1			C	HPO:probinson[2022-09-02]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0003477	PMID:36136249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0003202	PMID:36136249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0002059	PMID:36136249	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0002015	PMID:36136249	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0003621	PMID:36136249	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0002650	PMID:36136249	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0001272	PMID:36136249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0001260	PMID:36136249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0002075	PMID:36136249	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0001284	PMID:36136249	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0001251	PMID:36136249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0003391	PMID:36136249	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0011463	PMID:36136249	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0034332	PMID:36136249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0002317	PMID:36136249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0002505	PMID:36136249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0003701	PMID:36136249	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0001337	PMID:36136249	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620636	Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline		HP:0000006	PMID:36136249	PCS					I	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:175450	Polyposis, intestinal, with multiple exostoses		HP:0002762	OMIM:175450	IEA					P	HPO:iea[2009-02-17]
OMIM:175450	Polyposis, intestinal, with multiple exostoses		HP:0200008	OMIM:175450	IEA					P	HPO:iea[2009-02-17]
OMIM:175450	Polyposis, intestinal, with multiple exostoses		HP:0000006	OMIM:175450	IEA					I	HPO:iea[2009-02-17]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0002069	PMID:29539279	PCS		1/13			P	HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0003621	PMID:29539279	PCS		10/13			C	HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0002123	PMID:29539279	PCS		7/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0002373	PMID:29539279	PCS		4/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0002121	PMID:29539279	PCS		5/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0011463	PMID:29539279	PCS		1/13			C	HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0003829	PMID:29539279	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0000006	PMID:29539279	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-03-27]
OMIM:617924	Epilepsy, juvenile myoclonic, susceptibility to, 10		HP:0003623	PMID:29539279	PCS		1/13			C	HPO:probinson[2023-03-27]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002465	OMIM:608804	TAS					P	HPO:skoehler[2014-08-24]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002421	PMID:15192806	PCS		5/5			P	HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0010628	PMID:15192806	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0003431	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001332	OMIM:608804	TAS					P	HPO:skoehler[2014-08-24]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001250	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002384	PMID:15192806	PCS		3/5			P	HPO:probinson[2022-09-29];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002063	OMIM:608804	TAS					P	HPO:skoehler[2014-08-24]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001251	PMID:15192806	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0006808	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0003593	PMID:15192806	PCS		5/5			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001270	PMID:15192806	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0003390	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002080	OMIM:608804	TAS					P	HPO:probinson[2012-07-24]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0100543	OMIM:608804	TAS					P	HPO:probinson[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0000639	PMID:15192806	PCS		5/5			P	HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0007220	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002415	OMIM:608804	TAS					P	HPO:probinson[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002599	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002313	PMID:15192806	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0008936	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002059	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001583	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0003487	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001266	PMID:15192806	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001260	PMID:15192806	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0001263	OMIM:608804	TAS					P	HPO:skoehler[2014-04-04]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002191	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0000007	PMID:15192806	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0000648	OMIM:608804	IEA					P	HPO:iea[2009-02-17]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0002349	PMID:15192806	PCS		1/5			P	HPO:probinson[2022-09-29];HPO:probinson[2022-09-29]
OMIM:608804	Leukodystrophy, hypomyelinating, 2		HP:0000545	OMIM:608804	TAS					P	HPO:skoehler[2014-08-24]
OMIM:300705	Xp11.22 microduplication syndrome		HP:0000750	PMID:18252223	PCS					P	HPO:probinson[2013-02-17];HPO:probinson[2022-03-27]
OMIM:300705	Xp11.22 microduplication syndrome		HP:0011463	PMID:18252223	PCS					C	HPO:probinson[2022-03-27]
OMIM:300705	Xp11.22 microduplication syndrome		HP:0001417	PMID:18252223	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-03-27]
OMIM:300705	Xp11.22 microduplication syndrome		HP:0000256	PMID:18252223	PCS		4/10			P	HPO:probinson[2022-03-27]
OMIM:300705	Xp11.22 microduplication syndrome		HP:0001466	OMIM:300705	TAS					I	HPO:probinson[2025-09-26]
OMIM:300705	Xp11.22 microduplication syndrome		HP:0001249	PMID:18252223	PCS		10/10			P	HPO:probinson[2013-02-17];HPO:probinson[2022-03-27]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0003577	PMID:16505000	PCS		2/2			C	HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0008066	PMID:7509230;PMID:1380725	PCS		4/11			P	HPO:probinson[2023-07-07];HPO:probinson[2023-07-07];HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0005595	PMID:7509230;PMID:1380725;PMID:16505000	PCS		11/13			P	HPO:probinson[2023-07-07];HPO:probinson[2023-07-07];HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0000007	PMID:1380725	PCS					I	HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0001019	PMID:16505000	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0031288	PMID:16505000	PCS		1/2			P	HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0000972	PMID:7509230;PMID:16505000	PCS		2/10			P	HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0007479	PMID:16505000	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0000982	PMID:1380725	PCS		2/3			P	HPO:probinson[2023-07-07];HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0000006	PMID:7509230	PCS					I	HPO:probinson[2023-07-07]
OMIM:620150	Epidermolytic hyperkeratosis 2		HP:0000962	PMID:7509230	PCS		1/8			P	HPO:probinson[2023-07-07]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0000286	PMID:35390279	PCS		2/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0000582	PMID:35390279	PCS		1/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002268	PMID:35390279	PCS		1/5			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0003577	PMID:35390279	PCS		8/8			C	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002365	PMID:35390279	PCS		6/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001250	PMID:35390279	PCS		3/6			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002020	PMID:35390279	PCS		2/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001270	PMID:35390279	PCS		6/6			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0012110	PMID:35390279	PCS					P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0100307	PMID:35390279	PCS		6/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0000639	PMID:35390279	PCS		1/6			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001629	PMID:35390279	PCS		1/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0000316	PMID:35390279	PCS		1/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001643	PMID:35390279	PCS		1/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001320	PMID:35390279	PCS		5/5			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0008936	PMID:35390279	PCS		6/6			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001265	PMID:35390279	PCS		2/4			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002015	PMID:35390279	PCS		4/6			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002510	PMID:35390279	PCS		2/4			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001684	PMID:35390279	PCS		1/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001263	PMID:35390279	PCS		4/4			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0000294	PMID:35390279	PCS		1/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002093	PMID:35390279	PCS		5/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0000308	PMID:35390279	PCS		1/8			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002808	PMID:35390279	PCS		1/5			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0002509	PMID:35390279	PCS		6/6			P	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0000007	PMID:35390279	PCS					I	HPO:probinson[2022-08-17]
OMIM:619909	Pontocerebellar hypoplasia, type 17		HP:0001511	PMID:35390279	PCS		2/8			P	HPO:probinson[2022-08-17]
OMIM:610093	Microphthalmia, isolated 2		HP:0007759	PMID:17661825	PCS		6/6			P	HPO:probinson[2020-07-24];HPO:probinson[2022-11-24]
OMIM:610093	Microphthalmia, isolated 2		HP:0003577	PMID:17661825	PCS		6/6			C	HPO:probinson[2022-11-24]
OMIM:610093	Microphthalmia, isolated 2		HP:0000568	PMID:17661825	PCS		6/6		HP:0012828	P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-24];HPO:probinson[2022-11-24]
OMIM:610093	Microphthalmia, isolated 2		HP:0000007	PMID:17661825	PCS					I	HPO:probinson[2013-03-31];HPO:probinson[2020-07-24]
OMIM:610093	Microphthalmia, isolated 2		HP:0001249	PMID:17661825	PCS		0/6			P	HPO:probinson[2020-07-24];HPO:probinson[2022-11-24]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0003577	PMID:25900906	PCS		1/2			C	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000365	PMID:25900906	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000486	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000540	PMID:25900906	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0004322	PMID:25900906	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001250	OMIM:617930	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000160	PMID:25900906	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001251	OMIM:617930	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0003593	OMIM:617930	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0012427	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0011432	PMID:25900906	PCS		1/2			H	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0011220	PMID:25900906	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000316	OMIM:617930	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000219	PMID:25900906	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0025116	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000218	PMID:25900906	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000851	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001623	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001249	OMIM:617930	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000358	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0002058	PMID:25900906	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001385	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000252	OMIM:617930	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001344	PMID:25900906	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000431	OMIM:617930	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000276	OMIM:617930	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0009908	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0011968	PMID:25900906	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001382	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001260	PMID:25900906	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0025312	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0002033	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001263	PMID:25900906	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0012735	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0002194	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0034197	PMID:25900906	PCS		1/2			C	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000407	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0007874	PMID:25900906	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0004209	PMID:25900906	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0001511	PMID:25900906	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000006	PMID:25900906	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000028	OMIM:617930	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617930	Chromosome 1p35 deletion syndrome		HP:0000347	PMID:25900906	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0008969	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003236	PMID:14681890	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003555	OMIM:608810	IEA					P	HPO:iea[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003731	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003596	PMID:14681890	PCS		2/2			C	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003694	OMIM:608810	TAS					P	HPO:probinson[2012-07-27]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003493	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0002460	OMIM:608810	TAS					P	HPO:probinson[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0002380	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0012764	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0100324	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0000518	OMIM:608810	TAS					P	HPO:probinson[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0007340	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0009027	PMID:14681890	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003749	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003547	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0025717	PMID:14681890	PCS		2/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003325	OMIM:608810	IEA					P	HPO:iea[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0002015	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003581	OMIM:608810	IEA					C	HPO:iea[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003560	PMID:14681890	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0009072	OMIM:608810	IEA					P	HPO:iea[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0030207	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0001639	OMIM:608810	IEA					P	HPO:iea[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0002747	PMID:14681890	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003438	PMID:14681890	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0000006	PMID:14681890	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003677	PMID:14681890	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0003458	OMIM:608810	IEA					P	HPO:iea[2009-02-17]
OMIM:608810	Myopathy, myofibrillar, 2, mfm2		HP:0000467	OMIM:608810	IEA					P	HPO:iea[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0005216	OMIM:602483	PCS					P	HPO:probinson[2012-03-31]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000384	OMIM:602483	PCS					P	HPO:probinson[2012-03-31]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000160	PMID:16114046	PCS		52%			P	HPO:probinson[2012-03-31]
OMIM:602483	Auriculocondylar syndrome 1		HP:0025267	OMIM:602483	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000162	PMID:16114046	PCS		46%			P	HPO:probinson[2012-03-31]
OMIM:602483	Auriculocondylar syndrome 1		HP:0009088	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0009102	OMIM:602483	PCS					P	HPO:probinson[2012-03-31]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000678	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000378	OMIM:602483	PCS					P	HPO:probinson[2012-03-31]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000256	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000311	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000358	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0008537	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0008559	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000175	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0007627	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0007628	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0004453	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0004451	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0031013	OMIM:602483	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000689	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000006	OMIM:602483	IEA					I	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000369	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0002104	OMIM:602483	IEA					P	HPO:probinson[2009-02-17]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000402	PMID:16114046	PCS		30%			P	HPO:probinson[2012-03-31]
OMIM:602483	Auriculocondylar syndrome 1		HP:0000347	PMID:16114046	PCS		71%			P	HPO:probinson[2012-03-31]
OMIM:612690	Spherocytosis, type 5		HP:0005502	PMID:7803799	PCS					P	HPO:probinson[2019-06-04]
OMIM:612690	Spherocytosis, type 5		HP:0004444	PMID:7803799	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2019-06-04]
OMIM:612690	Spherocytosis, type 5		HP:0011893	PMID:7803799	PCS		0/1			P	HPO:probinson[2019-06-04];HPO:probinson[2022-04-16]
OMIM:612690	Spherocytosis, type 5		HP:0001878	PMID:7803799	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2019-06-04]
OMIM:612690	Spherocytosis, type 5		HP:0000007	PMID:7803799	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2019-06-04]
OMIM:612690	Spherocytosis, type 5		HP:0001923	PMID:7803799	PCS		1/1			P	HPO:probinson[2019-06-04]
OMIM:612690	Spherocytosis, type 5		HP:0011873	PMID:7803799	PCS		0/1			P	HPO:probinson[2019-06-04];HPO:probinson[2019-06-04];HPO:probinson[2022-04-16]
OMIM:612690	Spherocytosis, type 5		HP:0001744	PMID:7803799	PCS		1/1			P	HPO:probinson[2019-06-04]
OMIM:612690	Spherocytosis, type 5		HP:0000952	PMID:7803799	PCS		1/1			P	HPO:probinson[2019-06-04]
OMIM:615841	Spermatogenic failure 13		HP:0030345	PMID:24431330	PCS		0/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2021-11-11];HPO:probinson[2024-03-15]
OMIM:615841	Spermatogenic failure 13		HP:0011462	PMID:24431330	PCS		4/4			C	HPO:probinson[2021-11-11]
OMIM:615841	Spermatogenic failure 13		HP:0003251	PMID:24431330	PCS		3/4			P	HPO:probinson[2024-03-15]
OMIM:615841	Spermatogenic failure 13		HP:0008232	PMID:24431330	PCS		4/4			P	HPO:probinson[2024-03-15]
OMIM:615841	Spermatogenic failure 13		HP:0030087	PMID:24431330	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-11-11];HPO:probinson[2024-03-15]
OMIM:615841	Spermatogenic failure 13		HP:0000007	PMID:2443133	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-11-11]
OMIM:615841	Spermatogenic failure 13		HP:0040086	PMID:24431330	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-11-11];HPO:probinson[2024-03-15]
OMIM:615841	Spermatogenic failure 13		HP:0000027	PMID:24431330	PCS		3/4	MALE		P	HPO:skoehler[2014-07-11];HPO:probinson[2021-11-11]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0003577	PMID:9012405	PCS		2/2			C	HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0000992	PMID:9012405	PCS		2/2			P	HPO:skoehler[2015-09-22];HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0008064	PMID:9012405	PCS	HP:0003593	2/2			P	HPO:skoehler[2015-09-22];HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0004322	PMID:9012405	PCS		1/2			P	HPO:skoehler[2015-09-22];HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0000690	PMID:9012405	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0000007	PMID:9012405	PCS					I	HPO:skoehler[2015-09-22];HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0002208	PMID:9012405	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0045055	PMID:9012405	PCS		2/2			P	HPO:skoehler[2015-09-22];HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0007479	PMID:9012405	PCS	HP:0003577	2/2			P	HPO:skoehler[2015-09-22];HPO:probinson[2022-04-10]
OMIM:616390	Trichothiodystrophy 2, photosensitive		HP:0001249	PMID:9012405	PCS		0/2			P	HPO:skoehler[2015-09-22];HPO:probinson[2022-04-10]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0003577	PMID:26669664	PCS		2/2			C	HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0001498	PMID:26669664	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0004322	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0100864	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0012095	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0008450	PMID:26669664	PCS		2/2			P	HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0002999	PMID:26669664	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0001763	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0004976	PMID:26669664	PCS	HP:0003577	2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0003301	PMID:26669664	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0002650	PMID:26669664	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0003025	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0002651	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0031936	PMID:26669664	PCS		2/2			P	HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0003022	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0001382	PMID:26669664	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0000470	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0001182	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0003083	PMID:26669664	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0002827	PMID:26669664	PCS	HP:0003577	2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0000926	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0000007	PMID:26669664	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0000268	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0000883	OMIM:618395	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0001513	OMIM:618395	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618395	Spondyloepimetaphyseal dysplasia with joint laxity, type 3		HP:0001216	PMID:26669664	PCS		2/2			P	HPO:probinson[2022-10-11]
OMIM:243600	Jejunal atresia		HP:0005235	OMIM:243600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:243600	Jejunal atresia		HP:0001438	OMIM:243600	IEA					P	HPO:iea[2009-02-17]
OMIM:243600	Jejunal atresia		HP:0000007	OMIM:243600	IEA					I	HPO:iea[2009-02-17]
OMIM:619935	Immunodeficiency 106, susceptibility to viral infections		HP:0003621	PMID:31270247	PCS		1/2			C	HPO:probinson[2022-08-06]
OMIM:619935	Immunodeficiency 106, susceptibility to viral infections		HP:0020088	PMID:31270247	PCS		1/1			P	HPO:probinson[2022-08-06];HPO:probinson[2022-08-06]
OMIM:619935	Immunodeficiency 106, susceptibility to viral infections		HP:0003593	PMID:31270247	PCS		1/2			C	HPO:probinson[2022-08-06];HPO:probinson[2022-08-06]
OMIM:619935	Immunodeficiency 106, susceptibility to viral infections		HP:0034310	PMID:31270247	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:619935	Immunodeficiency 106, susceptibility to viral infections		HP:0000007	PMID:31270247	PCS					I	HPO:probinson[2022-08-06]
OMIM:134430	Factor VII and factor VIII, combined deficiency of		HP:0003125	OMIM:134430	TAS					P	HPO:probinson[2012-05-26]
OMIM:134430	Factor VII and factor VIII, combined deficiency of		HP:0002584	OMIM:134430	TAS					P	HPO:skoehler[2010-06-20]
OMIM:134430	Factor VII and factor VIII, combined deficiency of		HP:0008169	OMIM:134430	TAS					P	HPO:probinson[2012-05-26]
OMIM:134430	Factor VII and factor VIII, combined deficiency of		HP:0000006	OMIM:134430	TAS					I	HPO:probinson[2009-02-17]
OMIM:105835	Angel-Shaped phalangoepiphyseal dysplasia		HP:0001187	OMIM:105835	TAS					P	HPO:probinson[2012-07-29]
OMIM:105835	Angel-Shaped phalangoepiphyseal dysplasia		HP:0004322	OMIM:105835	TAS					P	HPO:probinson[2012-07-29]
OMIM:105835	Angel-Shaped phalangoepiphyseal dysplasia		HP:0003088	OMIM:105835	TAS					P	HPO:probinson[2012-07-29]
OMIM:105835	Angel-Shaped phalangoepiphyseal dysplasia		HP:0008843	OMIM:105835	TAS					P	HPO:probinson[2012-07-29]
OMIM:105835	Angel-Shaped phalangoepiphyseal dysplasia		HP:0001216	OMIM:105835	TAS					P	HPO:probinson[2012-07-29]
OMIM:105835	Angel-Shaped phalangoepiphyseal dysplasia		HP:0009193	OMIM:105835	TAS					P	HPO:probinson[2012-07-29]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0001508	PMID:21035102	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0011968	PMID:21035102	PCS		7/7			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-09-28]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0002153	OMIM:143860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0004906	PMID:21035102	PCS		5/7			P	HPO:probinson[2020-07-19];HPO:probinson[2022-09-28]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0003593	PMID:21035102	PCS		7/7			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0002902	OMIM:143860	TAS					P	HPO:skoehler[2013-01-22]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0000007	PMID:21035102	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:143860	Hyperchlorhidrosis, isolated		HP:0012236	PMID:21035102	PCS		7/7			P	HPO:probinson[2022-09-28]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0004732	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0003774	OMIM:174000	TAS					P	HPO:probinson[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0002048	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0000089	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0005576	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0001970	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0002120	OMIM:174000	IEA					P	HPO:skoehler[2019-04-18]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0003581	OMIM:174000	IEA					C	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0000096	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0005583	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0000092	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0012213	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0001903	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0000822	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0002615	OMIM:174000	TAS					P	HPO:probinson[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0000108	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0000006	PMID:23396133	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0003259	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0001997	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0000127	OMIM:174000	IEA					P	HPO:iea[2009-02-17]
OMIM:174000	Tubulointerstitial kidney disease, autosomal dominant, 2		HP:0002149	OMIM:174000	IEA					P	HPO:skoehler[2019-02-22]
OMIM:619921	Dystonia 35, childhood-onset		HP:0001332	PMID:34542157	PCS	HP:0003593	2/2			P	HPO:probinson[2022-08-14]
OMIM:619921	Dystonia 35, childhood-onset		HP:0001263	PMID:34542157	PCS		0/2			P	HPO:probinson[2022-08-14]
OMIM:619921	Dystonia 35, childhood-onset		HP:0003593	PMID:34542157	PCS		2/2			C	HPO:probinson[2022-08-14]
OMIM:619921	Dystonia 35, childhood-onset		HP:0000007	PMID:34542157	PCS					I	HPO:probinson[2022-08-14]
OMIM:619921	Dystonia 35, childhood-onset		HP:0001249	PMID:34542157	PCS		0/2			P	HPO:probinson[2022-08-14]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001650	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000286	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001770	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002188	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001531	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000486	PMID:16419126	PCS		4/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000365	PMID:16419126	PCS		6/14			P	HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0004322	OMIM:601808	TAS					P	HPO:probinson[2012-04-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001250	PMID:16419126	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0005134	OMIM:601808	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001252	PMID:16419126	PCS		10/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0005176	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0010806	OMIM:601808	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001290	OMIM:601808	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0012745	OMIM:601808	TAS					P	HPO:skoehler[2014-03-24]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000639	OMIM:601808	IEA		6/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000316	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001845	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0009623	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001643	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000510	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0003745	OMIM:601808	IEA					I	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001763	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001249	PMID:16419126	PCS		8/14			P	HPO:probinson[2012-04-09];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002311	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001265	PMID:16419126	PCS		7/14			P	HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000175	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000494	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000252	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000054	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000452	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0004970	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001382	PMID:16419126	PCS		6/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000294	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002072	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0011800	OMIM:601808	TAS					P	HPO:skoehler[2013-11-28]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000407	OMIM:601808	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000448	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001537	PMID:16419126	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000648	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000405	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000400	OMIM:601808	TAS					P	HPO:probinson[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000047	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000322	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002500	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000006	OMIM:601808	IEA					I	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000204	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000402	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001337	PMID:16419126	PCS		3/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000023	PMID:16419126	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000581	OMIM:601808	TAS					P	HPO:probinson[2012-04-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001270	OMIM:601808	TAS					P	HPO:probinson[2012-04-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001629	PMID:16419126	PCS		1/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000219	OMIM:601808	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002119	OMIM:601808	TAS					P	HPO:probinson[2012-04-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002714	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000413	PMID:16419126	PCS		7/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002136	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001047	OMIM:601808	TAS					P	HPO:probinson[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002650	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0004433	PMID:16419126	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001762	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001321	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001761	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002099	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000193	OMIM:601808	IEA		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000272	OMIM:601808	TAS					P	HPO:probinson[2012-04-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000470	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0005164	OMIM:601808	TAS					P	HPO:probinson[2012-04-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0005280	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001838	OMIM:601808	TAS					P	HPO:probinson[2012-04-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001635	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000824	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0002205	PMID:16419126	PCS		8/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001511	PMID:16419126	PCS		7/14			P	HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0001631	PMID:16419126	PCS		1/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000028	PMID:16419126	PCS		4/8	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:601808	Chromosome 18q deletion syndrome		HP:0000303	OMIM:601808	IEA					P	HPO:iea[2009-02-17]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0002069	PMID:30290154	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000341	PMID:30290154	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0003577	PMID:30290154	PCS		3/3			C	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0010803	PMID:30290154	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0001156	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0002002	PMID:30290154	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0002266	PMID:30290154	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0001252	PMID:30290154	PCS		2/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0010862	PMID:30290154	PCS		2/2			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0002080	PMID:30290154	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000639	PMID:30290154	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000998	PMID:30290154	PCS		3/3		HP:0012837	P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000219	PMID:30290154	PCS		3/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0002119	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000212	PMID:30290154	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0001249	PMID:30290154	PCS		3/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0001347	PMID:30290154	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000297	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000154	PMID:30290154	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0001385	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000750	PMID:30290154	PCS		2/2			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000574	PMID:30290154	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0002079	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0011968	PMID:30290154	PCS		2/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000490	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0001263	PMID:30290154	PCS		3/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0002194	PMID:30290154	PCS		2/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0011228	PMID:30290154	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000609	PMID:30290154	PCS		2/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0100874	PMID:30290154	PCS		3/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000527	PMID:30290154	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0004209	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000664	PMID:30290154	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000201	PMID:30290154	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000322	PMID:30290154	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000006	PMID:30290154	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000369	PMID:30290154	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:618381	Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome		HP:0000347	PMID:30290154	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-24]
OMIM:170500	Hyperkalemic periodic paralysis		HP:0003752	OMIM:170500	TAS					P	HPO:probinson[2012-04-11]
OMIM:170500	Hyperkalemic periodic paralysis		HP:0002486	OMIM:170500	TAS		HP:0040282			P	HPO:probinson[2012-04-11]
OMIM:170500	Hyperkalemic periodic paralysis		HP:0002153	OMIM:170500	IEA					P	HPO:skoehler[2019-09-07]
OMIM:170500	Hyperkalemic periodic paralysis		HP:0003593	OMIM:170500	IEA					C	HPO:iea[2009-02-17]
OMIM:170500	Hyperkalemic periodic paralysis		HP:6000833	PMID:20301669	PCS					P	HPO:probinson[2024-08-03]
OMIM:170500	Hyperkalemic periodic paralysis		HP:0007215	OMIM:170500	TAS					P	HPO:probinson[2012-04-11]
OMIM:170500	Hyperkalemic periodic paralysis		HP:0000006	OMIM:170500	TAS					I	HPO:probinson[2012-04-11]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0031956	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0000123	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0001894	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0030783	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0000790	PMID:21088618;PMID:9884342	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24];HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0001263	PMID:21088618	PCS		0/1			P	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0025289	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0002240	PMID:9884342	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0025420	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0000093	PMID:21088618;PMID:9884342	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24];HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0003281	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0031964	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0011227	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0012375	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0001878	PMID:9884342	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0100806	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0001746	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0000822	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0000007	PMID:9884342	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0002716	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0025435	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0001510	PMID:9884342	PCS	HP:0011463	1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0000421	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:614034	Heme oxygenase-1 deficiency		HP:0004844	PMID:21088618	PCS		1/1			P	HPO:probinson[2022-02-08]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001891	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0000585	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001596	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001096	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001250	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001394	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0002570	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001281	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0012115	OMIM:269200	TAS					P	HPO:skoehler[2013-01-22]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0100522	OMIM:269200	TAS					P	HPO:skoehler[2013-08-18]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0000518	OMIM:269200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001738	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0000836	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0033000	OMIM:269200	TAS					P	HPO:probinson[2022-09-07]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0002728	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001746	OMIM:269200	TAS					P	HPO:probinson[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0000007	OMIM:269200	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0000821	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0001426	OMIM:269200	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0200123	OMIM:269200	TAS					P	HPO:skoehler[2015-12-30]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0005978	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0000006	OMIM:269200	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:269200	Autoimmune polyendocrine syndrome, type II		HP:0008207	OMIM:269200	IEA					P	HPO:iea[2009-02-17]
OMIM:613983	Retinitis pigmentosa 60		HP:0001133	PMID:21549338	PCS		2/2			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0007737	PMID:21549338	PCS		1/1			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0000662	PMID:21549338	PCS		2/2			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0011462	PMID:21549338	PCS		2/2			C	HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0007663	PMID:21549338	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0000505	PMID:21549338	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0007994	PMID:21549338	PCS		2/2			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0000510	PMID:21549338	PCS		2/2			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0007787	PMID:21549338	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0000543	PMID:21549338	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0007722	PMID:21549338	PCS		1/1			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0007843	PMID:21549338	PCS		1/1			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:613983	Retinitis pigmentosa 60		HP:0000006	PMID:21549338	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0002850	PMID:31263572	PCS		2/2			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0005403	PMID:31263572	PCS		1/2			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0005479	PMID:31263572	PCS		1/2			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0003621	PMID:31263572	PCS		1/2			C	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0001531	PMID:31263572	PCS		1/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0020072	PMID:31263572	PCS		1/2			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0002013	PMID:31263572	PCS		2/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0030374	PMID:31263572	PCS					P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0003593	PMID:31263572	PCS		1/2			C	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0033454	PMID:31263572	PCS		1/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0040313	PMID:31263572	PCS		1/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0011473	PMID:31263572	PCS		1/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0000964	PMID:31263572	PCS		2/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0001019	PMID:31263572	PCS		1/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0001888	PMID:31263572	PCS		1/2			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0002205	PMID:31263572	PCS		2/2			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0001510	PMID:31263572	PCS		2/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0002206	PMID:31263572	PCS		1/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0000006	PMID:31263572	PCS					I	HPO:probinson[2021-10-24];HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0002720	PMID:31263572	PCS		2/2			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0002028	PMID:31263572	PCS		2/2			P	HP:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0004315	PMID:31263572	PCS		1/1			P	HPO:probinson[2021-10-24]
OMIM:619510	Immunodeficiency 85 and autoimmunity		HP:0040218	PMID:31263572	PCS		2/2			P	HPO:probinson[2021-10-24]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000242	OMIM:224300	IEA					P	HPO:iea[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0001474	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0003015	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000365	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000684	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0001476	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0006429	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0003498	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0001250	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0100923	OMIM:224300	TAS					P	HPO:probinson[2015-03-22]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000938	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0011220	OMIM:224300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000618	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0008479	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000879	OMIM:224300	TAS					P	HPO:probinson[2015-03-22]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000218	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002659	OMIM:224300	IEA					P	HPO:iea[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000774	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000311	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0006897	OMIM:224300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000773	OMIM:224300	TAS					P	HPO:probinson[2015-03-22]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000677	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0001249	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0003301	OMIM:224300	IEA					P	HPO:iea[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0007209	OMIM:224300	TAS					P	HPO:skoehler[2013-10-22]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000695	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0004334	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002870	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002694	OMIM:224300	TAS					P	HPO:iea[2015-03-22]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002376	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0005089	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0030320	OMIM:224300	TAS					P	HPO:probinson[2015-04-19]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0004054	OMIM:224300	IEA					P	HPO:iea[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0006480	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0006383	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000926	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000007	OMIM:224300	TAS					I	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000648	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002868	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002007	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002689	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000347	OMIM:224300	IEA					P	HPO:iea[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000941	OMIM:224300	TAS					P	HPO:iea[2015-03-22]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0002688	OMIM:224300	TAS					P	HPO:probinson[2009-02-17]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0000885	OMIM:224300	TAS					P	HPO:probinson[2015-03-22]
OMIM:224300	DYSOSTEOSCLEROSIS		HP:0005019	OMIM:224300	TAS					P	HPO:probinson[2015-03-22]
OMIM:618168	Diarrhea 9		HP:0002014	PMID:27640305;OMIM:618168	IEA		20/20			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-07]
OMIM:618168	Diarrhea 9		HP:0001508	OMIM:618168	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618168	Diarrhea 9		HP:0011473	PMID:27640305	PCS					P	HPO:probinson[2019-09-07]
OMIM:618168	Diarrhea 9		HP:0000007	PMID:29909964	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-09-07]
OMIM:272620	Tardive dyskinesia		HP:0000007	OMIM:272620	IEA					I	HPO:iea[2009-02-17]
OMIM:272620	Tardive dyskinesia		HP:0040141	OMIM:272620	TAS					P	HPO:skoehler[2015-01-26]
OMIM:272620	Tardive dyskinesia		HP:0031943	OMIM:272620	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616145	Catel-Manzke syndrome		HP:0001651	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001250	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000160	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001373	OMIM:616145	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616145	Catel-Manzke syndrome		HP:0000162	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0010049	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0010763	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0045074	PMID:25480037	PCS		3/5			P	HPO:probinson[2023-04-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0009464	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000316	PMID:25480037	PCS		3/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000954	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0008897	PMID:25480037	PCS		2/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0002857	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000476	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000175	PMID:25480037	PCS		6/7			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000293	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001382	PMID:25480037	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001263	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001181	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0012385	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000767	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001537	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000007	PMID:25480037	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0004209	PMID:25480037	PCS		3/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000768	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0009933	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0002623	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000201	PMID:25480037	PCS		7/7			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000520	PMID:25480037	PCS		1/5		HP:0012825	P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000204	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000369	PMID:25480037	PCS		2/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000582	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0003577	PMID:25480037	PCS		7/7			C	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000023	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000460	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0003097	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0005792	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001629	PMID:25480037	PCS		2/7			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000579	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000218	PMID:25480037	PCS		1/7			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0030368	OMIM:616145	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616145	Catel-Manzke syndrome		HP:0002650	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001762	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000193	PMID:25480037	PCS		1/7			P	HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001680	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000470	PMID:25480037	PCS		1/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001511	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000028	OMIM:616145	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616145	Catel-Manzke syndrome		HP:0000347	PMID:25480037	PCS		5/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-04]
OMIM:616145	Catel-Manzke syndrome		HP:0001831	PMID:25480037	PCS		1/5			P	HPO:probinson[2023-04-04]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0003510	PMID:22121204	PCS		1/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0003577	PMID:22121204	PCS		2/2			C	HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0002650	PMID:22121204	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0000407	PMID:22121204	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0001839	PMID:22121204	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0000007	PMID:22121204	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0001171	PMID:22121204	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0001182	PMID:22121204	PCS		1/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-09-27]
OMIM:220600	Split-Hand/foot malformation 1 with sensorineural hearing loss		HP:0002007	PMID:22121204	PCS		1/2			P	HPO:probinson[2022-09-27]
OMIM:602124	Dystonia 7, torsion		HP:0000473	OMIM:602124	IEA					P	HPO:iea[2009-02-17]
OMIM:602124	Dystonia 7, torsion		HP:0002312	OMIM:602124	IEA					P	HPO:iea[2009-02-17]
OMIM:602124	Dystonia 7, torsion		HP:0002356	OMIM:602124	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602124	Dystonia 7, torsion		HP:0002378	OMIM:602124	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602124	Dystonia 7, torsion		HP:0001618	OMIM:602124	IEA					P	HPO:iea[2009-02-17]
OMIM:602124	Dystonia 7, torsion		HP:0012048	OMIM:602124	IEA					P	HPO:iea[2009-02-17]
OMIM:602124	Dystonia 7, torsion		HP:0003712	OMIM:602124	IEA					P	HPO:iea[2009-02-17]
OMIM:602124	Dystonia 7, torsion		HP:0000006	OMIM:602124	IEA					I	HPO:iea[2009-02-17]
OMIM:602124	Dystonia 7, torsion		HP:0001304	OMIM:602124	IEA					P	HPO:iea[2009-02-17]
OMIM:602124	Dystonia 7, torsion		HP:0000643	OMIM:602124	IEA					P	HPO:iea[2009-02-17]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0000506	PMID:23818446	PCS		8/8			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0000482	PMID:23818446	PCS		8/8			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0000007	PMID:23818446	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0000455	PMID:23818446	PCS		3/8			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0007787	PMID:23818446	PCS		1/8			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0200065	PMID:23818446	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0000358	PMID:23818446	PCS		8/8			P	HPO:skoehler[2013-11-18]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0000545	PMID:23818446	PCS		8/8			P	HPO:probinson[2023-02-25]
OMIM:615458	Microcornea, myopic chorioretinal atrophy, and telecanthus		HP:0000445	PMID:23818446	PCS		2/8			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:219095	Cutaneous photosensitivity and colitis, lethal		HP:0002014	OMIM:219095	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219095	Cutaneous photosensitivity and colitis, lethal		HP:0002583	OMIM:219095	IEA					P	HPO:iea[2009-02-17]
OMIM:219095	Cutaneous photosensitivity and colitis, lethal		HP:0007396	OMIM:219095	IEA					P	HPO:iea[2009-02-17]
OMIM:219095	Cutaneous photosensitivity and colitis, lethal		HP:0000007	OMIM:219095	IEA					I	HPO:iea[2009-02-17]
OMIM:219095	Cutaneous photosensitivity and colitis, lethal		HP:0010783	OMIM:219095	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219095	Cutaneous photosensitivity and colitis, lethal		HP:0001522	OMIM:219095	IEA					C	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0003411	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0002650	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0000540	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0001552	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0002176	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0000470	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0100864	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0002808	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0000926	PMID:18587396	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0009466	OMIM:113500	IEA					P	HPO:iea[2009-02-17]
OMIM:113500	Brachyolmia type 3		HP:0030084	OMIM:113500	TAS					P	HPO:skoehler[2014-09-21]
OMIM:113500	Brachyolmia type 3		HP:0000006	PMID:18587396	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:113500	Brachyolmia type 3		HP:0001249	PMID:18587396	PCS		0/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:113500	Brachyolmia type 3		HP:0008922	PMID:18587396	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000286	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0004322	PMID:24193349	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0010945	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001250	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0002121	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001252	OMIM:612337	TAS					P	HPO:skoehler[2014-11-26]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001274	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0002020	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0003593	PMID:26740508	PCS		1/1			C	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0012745	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001290	OMIM:612337	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000319	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0011220	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000316	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0003508	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000219	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0012171	PMID:26740508	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000311	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000377	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001249	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0002553	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0003763	PMID:26740508	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000252	PMID:24193349	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0003189	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000750	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001344	OMIM:612337	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0002376	PMID:26740508	IEA		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0011968	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001263	PMID:24193349	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0005280	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0002190	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000506	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001511	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000322	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001510	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000347	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000369	OMIM:612337	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0000006	PMID:24193349	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:612337	Intellectual developmental disorder, autosomal dominant 22		HP:0001611	PMID:24193349	PCS		1/1			P	HPO:probinson[2022-06-11]
OMIM:613029	Glioma susceptibility 3		HP:0009592	PMID:16825431	PCS		2/28			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-08]
OMIM:613029	Glioma susceptibility 3		HP:0006727	PMID:16825431	PCS		3/28			P	HPO:probinson[2023-05-08]
OMIM:613029	Glioma susceptibility 3		HP:0012174	PMID:15689453	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-08]
OMIM:613029	Glioma susceptibility 3		HP:0004808	PMID:16825431	PCS		10/28			P	HPO:probinson[2023-05-08]
OMIM:613029	Glioma susceptibility 3		HP:0000007	PMID:15689453	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:613029	Glioma susceptibility 3		HP:0002667	PMID:16825431;PMID:15689453	PCS		9/30			P	HPO:probinson[2023-05-08]
OMIM:613029	Glioma susceptibility 3		HP:0004812	PMID:16825431;PMID:15689453	PCS		2/30			P	HPO:probinson[2023-05-08]
OMIM:613029	Glioma susceptibility 3		HP:0002885	PMID:16825431;PMID:15689453	PCS		8/30			P	HPO:probinson[2023-05-08];HPO:skoehler[2015-12-30];HPO:probinson[2023-05-08]
OMIM:129850	Edinburgh malformation syndrome		HP:0001508	OMIM:129850	IEA					P	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0003265	OMIM:129850	IEA					P	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0010806	OMIM:129850	TAS					P	HPO:probinson[2022-08-18]
OMIM:129850	Edinburgh malformation syndrome		HP:0000238	OMIM:129850	IEA					P	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0011335	OMIM:129850	TAS					P	HPO:probinson[2022-08-18]
OMIM:129850	Edinburgh malformation syndrome		HP:0001270	OMIM:129850	IEA					P	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0001522	OMIM:129850	IEA					C	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0005616	OMIM:129850	IEA					P	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0000006	OMIM:129850	IEA					I	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0000952	OMIM:129850	IEA					P	HPO:iea[2009-02-17]
OMIM:129850	Edinburgh malformation syndrome		HP:0001249	OMIM:129850	IEA					P	HPO:skoehler[2010-06-18]
OMIM:616151	Macular dystrophy, vitelliform, 4		HP:0003581	PMID:23993198	PCS		8/8			C	HPO:probinson[2021-10-13];HPO:probinson[2021-10-13]
OMIM:616151	Macular dystrophy, vitelliform, 4		HP:0008179	PMID:23993198	PCS		7/8			P	HPO:probinson[2021-10-13]
OMIM:616151	Macular dystrophy, vitelliform, 4		HP:0011510	PMID:23993198	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-12]
OMIM:616151	Macular dystrophy, vitelliform, 4		HP:0007754	PMID:23993198	PCS					P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616151	Macular dystrophy, vitelliform, 4		HP:0007677	PMID:23993198	PCS		8/8			P	HPO:skoehler[2015-09-15];HPO:probinson[2021-10-13]
OMIM:616151	Macular dystrophy, vitelliform, 4		HP:0000006	PMID:23993198	PCS					I	HPO:skoehler[2015-09-15];HPO:probinson[2021-10-13]
OMIM:616151	Macular dystrophy, vitelliform, 4		HP:0030515	PMID:23993198	PCS		5/8			P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:117000	Central core disease		HP:0002047	OMIM:117000;PMID:11113224	PCS		2/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0001374	OMIM:117000	IEA					P	HPO:iea[2009-02-17]
OMIM:117000	Central core disease		HP:0003593	PMID:11113224	PCS		8/8			C	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0001270	PMID:16940308;PMID:11113224	PCS		6/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26];HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0030319	PMID:11113224	PCS		7/8			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0003803	OMIM:117000	IEA					P	HPO:iea[2009-02-17]
OMIM:117000	Central core disease		HP:0001324	PMID:16940308	PCS	HP:0003623	4/4			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0001763	OMIM:117000	IEA					P	HPO:iea[2009-02-17]
OMIM:117000	Central core disease		HP:0003623	PMID:16940308	PCS		4/4			C	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0003202	OMIM:117000	IEA					P	HPO:iea[2009-02-17]
OMIM:117000	Central core disease		HP:0001265	PMID:11113224	PCS		6/8			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0003324	OMIM:117000	IEA					P	HPO:iea[2009-02-17]
OMIM:117000	Central core disease		HP:0003687	PMID:11113224	PCS		2/2			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0001883	PMID:16940308	PCS		1/4			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0002650	PMID:11113224	PCS		1/8			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0031936	PMID:16940308	PCS		4/4			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0011968	PMID:16940308	PCS		4/4			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0030230	PMID:16940308	PCS		3/3			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0000007	PMID:16940308	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0001319	PMID:16940308	PCS	HP:0003623	4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0006466	PMID:11113224	PCS		6/8			P	HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0000006	OMIM:117000	IEA					I	HPO:iea[2009-02-17]
OMIM:117000	Central core disease		HP:0003798	PMID:11113224	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-06-26]
OMIM:117000	Central core disease		HP:0003677	OMIM:117000	TAS					C	HPO:skoehler[2012-11-16]
OMIM:117000	Central core disease		HP:0003557	PMID:16940308;PMID:11113224	PCS		5/5			P	HPO:probinson[2021-06-26]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000582	PMID:33909992	PCS		3/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000486	PMID:33909992	PCS		6/23			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0004322	PMID:33909992	PCS		12/31			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000122	PMID:33909992	PCS		3/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0001250	PMID:33909992	PCS		9/33			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0410030	PMID:33909992	PCS		1/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0001270	PMID:33909992	PCS		20/29			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0002719	PMID:33909992	PCS		11/33			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000319	PMID:33909992	PCS		1/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0008897	PMID:33909992	PCS		9/30			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000219	PMID:33909992	PCS		12/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000256	PMID:33909992	PCS		4/31			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000454	PMID:33909992	PCS		9/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000252	PMID:33909992	PCS		7/31			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000175	PMID:33909992	PCS		1/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000750	PMID:33909992	PCS		29/32			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0002353	PMID:33909992	PCS		10/23			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0002650	PMID:33909992	PCS		3/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0009928	PMID:33909992	PCS		9/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0002750	PMID:33909992	PCS		2/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0011968	PMID:33909992	PCS		11/27			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0001382	PMID:33909992	PCS		9/29			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000490	PMID:33909992	PCS		5/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0001263	PMID:33909992	PCS		31/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0011800	PMID:33909992	PCS		5/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0009890	PMID:33909992	PCS		4/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000729	PMID:33909992	PCS		8/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000629	PMID:33909992	PCS		6/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0007874	PMID:33909992	PCS		8/24			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0007018	PMID:33909992	PCS		4/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000201	PMID:33909992	PCS		2/34			P	HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000322	PMID:33909992	PCS		1/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000006	PMID:33909992	PCS					I	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000325	PMID:33909992	PCS		10/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:619504	Chopra-Amiel-Gordon syndrome		HP:0000248	PMID:33909992	PCS		3/24			P	HPO:probinson[2021-09-18];HPO:probinson[2021-09-18]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0003577	PMID:20583171	PCS		1/1			C	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0008905	PMID:20583171	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000463	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0003498	PMID:20583171	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000023	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0004322	PMID:9843043	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0001371	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0003273	PMID:9843043	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0001252	PMID:9843043	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0005792	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0001290	OMIM:222765	TAS					P	HPO:skoehler[2017-07-13]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0010920	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000518	PMID:9843043	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0001508	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000938	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:4000165	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000239	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000218	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0002832	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0001249	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0003301	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000176	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000252	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0002650	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000431	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0008838	PMID:20583171	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0011800	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:6000426	PMID:9843043	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0005280	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0010655	PMID:20583171;PMID:9843043	PCS		2/2			P	HPO:probinson[2023-02-12];HPO:probinson[2024-02-27]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000609	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0034671	PMID:9843043	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0001636	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000007	PMID:9536089	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000348	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0003417	PMID:20583171	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0000347	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:222765	Rhizomelic chondrodysplasia punctata, type 2		HP:0002644	OMIM:222765	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001374	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0004322	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000160	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001032	PMID:8923936	PCS		11/15			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0003273	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001290	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001193	PMID:8923936	PCS		8/15			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001848	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001845	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000954	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0009742	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000278	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001249	PMID:8923936	PCS		0/15			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001188	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0002650	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001762	PMID:8923936	PCS		9/15			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000211	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0003184	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001181	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0010557	PMID:8923936	PCS		14/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0012385	PMID:8923936	PCS		6/15			P	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0006380	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0001838	PMID:8923936;OMIM:108120	PCS		11/25			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0009473	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0033142	PMID:23678273	PCS					P	HPO:probinson[2020-10-13]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000407	OMIM:108120	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000508	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0002804	OMIM:108120	IEA					P	HPO:skoehler[2015-01-27]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0002987	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000465	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000006	PMID:8923936	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000028	OMIM:108120	IEA					P	HPO:iea[2009-02-17]
OMIM:108120	Arthrogryposis, distal, type 1A		HP:0000369	OMIM:108120	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610246	Spinocerebellar ataxia 28		HP:0003621	PMID:16251216	PCS		1/11			C	HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0000640	PMID:16251216	PCS		5/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0001300	OMIM:610246	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610246	Spinocerebellar ataxia 28		HP:0003200	PMID:16251216	PCS		0/4			P	HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0003487	PMID:16251216	PCS		4/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0001332	OMIM:610246	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610246	Spinocerebellar ataxia 28		HP:0001272	PMID:16251216	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0002395	PMID:16251216	PCS		9/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0001260	PMID:16251216	PCS		9/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0002066	PMID:16251216	PCS		11/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0003474	PMID:16251216	PCS		0/6			P	HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0002070	PMID:16251216	PCS		10/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0011922	PMID:16251216	PCS		0/4			P	HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0011462	PMID:16251216	PCS		10/11			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0000508	PMID:16251216	PCS		6/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0000514	PMID:16251216	PCS		6/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0006895	PMID:16251216	PCS		2/5			P	HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0000641	PMID:16251216	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0000597	PMID:16251216	PCS		8/11			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0001257	OMIM:610246	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610246	Spinocerebellar ataxia 28		HP:0000006	PMID:20208537	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:610246	Spinocerebellar ataxia 28		HP:0003677	PMID:16251216	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-08]
OMIM:193300	von Hippel-Lindau syndrome		HP:0002894	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	Von hippel-lindau syndrome		HP:0031207	OMIM:193300	TAS					P	HPO:probinson[2022-07-01]
OMIM:193300	von Hippel-Lindau syndrome		HP:0030424	OMIM:193300	TAS					P	HPO:skoehler[2015-07-26]
OMIM:193300	von Hippel-Lindau syndrome		HP:0002321	PMID:17609489	PCS		24/35			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-07-01]
OMIM:193300	von Hippel-Lindau syndrome		HP:0005584	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0005562	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0000360	PMID:17609489	PCS		27/35			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-07-01]
OMIM:193300	von Hippel-Lindau syndrome		HP:0000407	PMID:17609489	PCS		34/35			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-01]
OMIM:193300	Von hippel-lindau syndrome		HP:0011462	PMID:17609489	PCS					C	HPO:probinson[2022-07-01]
OMIM:193300	von Hippel-Lindau syndrome		HP:0006880	OMIM:193300	TAS					P	HPO:probinson[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0000822	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0009711	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0001737	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0001901	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0009713	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0002668	OMIM:193300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0009715	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0000006	OMIM:193300	IEA					I	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0005954	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:193300	von Hippel-Lindau syndrome		HP:0002666	OMIM:193300	IEA					P	HPO:iea[2009-02-17]
OMIM:614020	Intellectual developmental disorder, autosomal recessive 14		HP:0000189	PMID:21212097	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-15]
OMIM:614020	Intellectual developmental disorder, autosomal recessive 14		HP:0000750	PMID:21212097	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-15]
OMIM:614020	Intellectual developmental disorder, autosomal recessive 14		HP:0003593	PMID:21212097	PCS		4/4			C	HPO:probinson[2022-06-15]
OMIM:614020	Intellectual developmental disorder, autosomal recessive 14		HP:0000007	PMID:21212097	PCS					I	HPO:probinson[2013-04-07];HPO:probinson[2022-06-15]
OMIM:614020	Intellectual developmental disorder, autosomal recessive 14		HP:0002080	PMID:21212097	PCS		3/4			P	HPO:probinson[2022-06-15]
OMIM:614020	Intellectual developmental disorder, autosomal recessive 14		HP:0001249	PMID:21212097	PCS		4/4			P	HPO:probinson[2013-04-07];HPO:probinson[2022-06-15]
OMIM:604233	Generalized epilepsy with febrile seizures plus, type 1		HP:0002069	OMIM:604233	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604233	Generalized epilepsy with febrile seizures plus, type 1		HP:0002373	OMIM:604233	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604233	Generalized epilepsy with febrile seizures plus, type 1		HP:0002121	OMIM:604233	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604233	Generalized epilepsy with febrile seizures plus, type 1		HP:0010819	OMIM:604233	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604233	Generalized epilepsy with febrile seizures plus, type 1		HP:0003829	OMIM:604233	TAS					I	HPO:skoehler[2012-10-17]
OMIM:604233	Generalized epilepsy with febrile seizures plus, type 1		HP:0000006	OMIM:604233	TAS					I	HPO:skoehler[2012-10-17]
OMIM:601363	Wilms tumor 4		HP:0002667	OMIM:601363	IEA					P	HPO:iea[2009-02-17]
OMIM:601363	Wilms tumor 4		HP:0000006	OMIM:601363	IEA					I	HPO:iea[2009-02-17]
OMIM:618632	Usher syndrome, type 1M		HP:0001751	PMID:29572253	PCS	HP:0003593	5/5			P	HPO:probinson[2020-06-13]
OMIM:618632	Usher syndrome, type 1M		HP:0000662	PMID:29572253	PCS		5/5			P	HPO:probinson[2020-06-13]
OMIM:618632	Usher syndrome, type 1M		HP:0000007	PMID:29572253	PCS					I	HPO:probinson[2020-06-12];HPO:probinson[2020-06-12]
OMIM:618632	Usher syndrome, type 1M		HP:0001712	PMID:29572253	PCS		2/5			P	HPO:probinson[2020-06-13]
OMIM:618632	Usher syndrome, type 1M		HP:0011510	PMID:29572253	PCS		5/5			P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618632	Usher syndrome, type 1M		HP:0000543	PMID:29572253	PCS		4/5			P	HPO:probinson[2020-06-13]
OMIM:618632	Usher syndrome, type 1M		HP:0000399	PMID:29572253	PCS	HP:0003593	5/5			P	HPO:probinson[2020-06-13]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002389	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0004322	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001371	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0045075	PMID:21932319	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000958	PMID:21932319	PCS		2/2			P	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0011463	PMID:21932319	PCS		4/4			C	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16];HPO:probinson[2022-05-08]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000678	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0005328	PMID:21549337;PMID:21932319	PCS		3/4			P	HPO:probinson[2021-10-16];HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001387	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0005585	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0011800	PMID:21932319	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0100578	PMID:21549337;PMID:21932319	PCS		3/4			P	HP:probinson[2021-10-16];HPO:skoehler[2012-11-18];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000689	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000007	PMID:21549337	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0008404	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000444	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000883	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000520	PMID:21932319	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16];HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001015	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001653	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002621	PMID:21932319	PCS		0/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001476	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0009839	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001596	PMID:21932319	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0011712	PMID:21932319	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0030718	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002280	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0003292	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000939	PMID:21932319	PCS		4/4			P	HP:probinson[2021-10-16];HPO:skoehler[2012-11-18];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001508	PMID:21932319	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16];HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0031295	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0034047	PMID:21932319	PCS		2/2			P	HPO:probinson[2022-02-27]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0034046	PMID:21932319	PCS		4/4			P	HPO:probinson[2022-02-03];HPO:probinson[2022-02-27]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000653	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002756	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002797	PMID:21932319	PCS		4/4			P	HP:probinson[2021-10-16];HPO:skoehler[2012-11-18];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002996	PMID:21932319	PCS		2/2			P	HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000233	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002650	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002094	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002092	PMID:21932319	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0011703	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0010537	PMID:21932319	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000308	PMID:21932319	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000905	PMID:21932319	PCS		2/2			P	HPO:skoehler[2012-11-19];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0002209	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000822	PMID:21932319	PCS		0/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0001510	PMID:21932319	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614008	Nestor-Guillermo progeria syndrome		HP:0000347	PMID:21549337	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-16]
OMIM:613767	Retinitis pigmentosa 45		HP:0007737	PMID:11379879	PCS		1/1			P	HPO:probinson[2013-02-17];HPO:probinson[2022-11-21]
OMIM:613767	Retinitis pigmentosa 45		HP:0000662	PMID:11379879	PCS	HP:0011463	1/1			P	HPO:probinson[2013-02-17];HPO:probinson[2022-11-21]
OMIM:613767	Retinitis pigmentosa 45		HP:0000608	OMIM:613767	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:613767	Retinitis pigmentosa 45		HP:0000007	PMID:11379879	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-11-21]
OMIM:613767	Retinitis pigmentosa 45		HP:0007994	PMID:11379879	PCS		1/1			P	HPO:probinson[2013-02-17];HPO:probinson[2022-11-21]
OMIM:613767	Retinitis pigmentosa 45		HP:0000510	PMID:11379879	PCS		1/1			P	HPO:probinson[2013-02-17];HPO:probinson[2022-11-21]
OMIM:613767	Retinitis pigmentosa 45		HP:0000512	PMID:11379879	PCS		1/1			P	HPO:probinson[2022-11-21]
OMIM:217090	Plasminogen deficiency, type I		HP:0000230	OMIM:217090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217090	Plasminogen deficiency, type I		HP:0000123	OMIM:217090	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:217090	Plasminogen deficiency, type I		HP:0001321	PMID:9242524	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0003593	PMID:9242524;OMIM:217090	PCS		11/12			C	HPO:probinson[2022-08-13];HPO:iea[2009-02-17]
OMIM:217090	Plasminogen deficiency, type I		HP:0001290	PMID:9242524	PCS		1/2			P	HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0034197	PMID:9242524	PCS		1/2			C	HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0000704	OMIM:217090	IEA					P	HPO:iea[2009-02-17]
OMIM:217090	Plasminogen deficiency, type I		HP:0000509	PMID:9242524	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0000618	OMIM:217090	IEA					P	HPO:iea[2009-02-17]
OMIM:217090	Plasminogen deficiency, type I		HP:0001977	PMID:9242524	PCS		0/2			P	HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0000238	PMID:9242524	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0001305	PMID:9242524	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0000007	PMID:9242524	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0002119	PMID:9242524	PCS		1/2			P	HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0002788	OMIM:217090	IEA					P	HPO:iea[2009-02-17]
OMIM:217090	Plasminogen deficiency, type I		HP:0040228	PMID:9242524	PCS		2/2			P	HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0000256	PMID:9242524	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0000212	PMID:9242524	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:217090	Plasminogen deficiency, type I		HP:0000787	OMIM:217090	IEA					P	HPO:iea[2009-02-17]
OMIM:217090	Plasminogen deficiency, type I		HP:0002588	OMIM:217090	IEA					P	HPO:iea[2009-02-17]
OMIM:217090	Plasminogen deficiency, type I		HP:0000951	OMIM:217090	IEA					P	HPO:iea[2009-02-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0003577	PMID:26942290	PCS		5/5			C	HPO:probinson[2023-02-25]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001596	PMID:26942290	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001250	PMID:26942290	PCS		1/5			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-25]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001274	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001031	OMIM:613001	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0100251	OMIM:613001	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001629	OMIM:613001	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0100702	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0012032	OMIM:613001	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0002539	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001305	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0000238	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0003745	OMIM:613001	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0007546	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001682	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001321	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0002079	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001442	PMID:26942290	PCS		20/20			I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-25];HPO:probinson[2023-02-25]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001140	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0002132	OMIM:613001	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001263	PMID:26942290	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0034587	PMID:26942290	PCS		5/5			P	HPO:probinson[2023-03-31]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0009592	PMID:26942290	PCS		2/5			P	HPO:probinson[2023-02-25]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0000568	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0004969	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0000625	PMID:26942290	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-25]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0007676	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0000647	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0000125	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0001631	OMIM:613001	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0000028	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613001	Encephalocraniocutaneous lipomatosis		HP:0000126	OMIM:613001	TAS					P	HPO:skoehler[2012-10-17]
OMIM:161800	Nemaline myopathy 3		HP:0001276	OMIM:161800	TAS		HP:0040283			P	HPO:skoehler[2013-06-06]
OMIM:161800	Nemaline myopathy 3		HP:0010628	OMIM:161800	TAS					P	HPO:skoehler[2015-01-04]
OMIM:161800	Nemaline myopathy 3		HP:0002063	OMIM:161800	TAS		HP:0040283			P	HPO:skoehler[2013-06-06]
OMIM:161800	Nemaline myopathy 3		HP:0003690	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0001270	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0008872	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0002515	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0003307	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0003803	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0000218	OMIM:161800	TAS					P	HPO:iea[2013-08-11]
OMIM:161800	Nemaline myopathy 3		HP:0003701	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0002359	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0003306	OMIM:161800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:161800	Nemaline myopathy 3		HP:0000278	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0003722	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0001347	OMIM:161800	TAS		HP:0040283			P	HPO:skoehler[2013-06-06]
OMIM:161800	Nemaline myopathy 3		HP:0001644	OMIM:161800	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:161800	Nemaline myopathy 3		HP:0002058	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0001265	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0001561	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0003324	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0003445	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0002015	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0002650	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0001761	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0000298	OMIM:161800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:161800	Nemaline myopathy 3		HP:0001283	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0001284	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0002093	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0008180	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0001558	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0000007	OMIM:161800	TAS					I	HPO:skoehler[2015-12-30]
OMIM:161800	Nemaline myopathy 3		HP:0002804	OMIM:161800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:161800	Nemaline myopathy 3		HP:0001319	OMIM:161800	IEA					P	HPO:iea[2009-02-17]
OMIM:161800	Nemaline myopathy 3		HP:0002747	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0001533	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0003798	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0000006	OMIM:161800	IEA					I	HPO:iea[2009-02-17]
OMIM:161800	Nemaline myopathy 3		HP:0003810	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:161800	Nemaline myopathy 3		HP:0003458	OMIM:161800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0000582	PMID:28985353	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0001561	PMID:28985353	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0003577	PMID:28985353	PCS		2/2			C	HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0000486	PMID:28985353	PCS		2/2			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0002243	PMID:28985353	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0000034	PMID:28985353	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0000463	PMID:28985353	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0002076	PMID:28985353	PCS		1/2			P	HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0011968	PMID:28985353	PCS		1/2			P	HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0012368	PMID:28985353	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0000316	PMID:28985353	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0000007	PMID:28985353	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0002108	PMID:28985353	PCS		1/2			P	HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0000664	PMID:28985353	PCS		1/2			P	HPO:probinson[2023-03-03]
OMIM:618154	Hennekam lymphangiectasia-lymphedema syndrome 3		HP:0001004	PMID:28985353	PCS	HP:0003577	2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-03]
OMIM:610508	Maturity-onset diabetes of the young, type VII		HP:0004904	PMID:15774581	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-20]
OMIM:610508	Maturity-onset diabetes of the young, type VII		HP:0005978	PMID:15774581	PCS					P	HPO:probinson[2013-02-28]
OMIM:610508	Maturity-onset diabetes of the young, type VII		HP:0000006	PMID:15774581	PCS					I	HPO:probinson[2013-01-09]
OMIM:618140	Deafness, autosomal dominant 74		HP:0001751	PMID:29860631	PCS		0/28			P	HPO:probinson[2023-02-11]
OMIM:618140	Deafness, autosomal dominant 74		HP:0000407	PMID:29860631	PCS		28/28			P	HPO:probinson[2023-02-11]
OMIM:618140	Deafness, autosomal dominant 74		HP:0003581	PMID:29860631	PCS					C	HPO:probinson[2023-02-11]
OMIM:618140	Deafness, autosomal dominant 74		HP:0000006	PMID:29860631	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-11]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0002322	OMIM:607060	IEA					P	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0001300	OMIM:607060	IEA					P	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0002067	OMIM:607060	IEA					P	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0003584	PMID:15541308	PCS					C	HPO:probinson[2022-06-26]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0002063	OMIM:607060	IEA					P	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0002172	OMIM:607060	IEA					P	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0011960	OMIM:607060	TAS					P	HPO:probinson[2012-07-18]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0100315	OMIM:607060	TAS					P	HPO:skoehler[2015-12-30]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0000726	OMIM:607060	IEA					P	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0003829	OMIM:607060	TAS					I	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0004409	OMIM:607060	IEA					P	HPO:skoehler[2010-06-18]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0002548	OMIM:607060	IEA					P	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0000006	OMIM:607060	IEA					I	HPO:iea[2009-02-17]
OMIM:607060	Parkinson disease 8, autosomal dominant		HP:0003677	OMIM:607060	IEA					C	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002421	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002540	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000486	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001332	PMID:20799324	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0004322	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001250	PMID:20799324	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001250	PMID:17846997	PCS	HP:0003623	5/19			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002062	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000639	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0007321	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000873	PMID:25604658	PCS		3/79			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0009704	PMID:16845398	PCS		23/23			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000253	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000252	PMID:17357087;PMID:20799324	PCS		2/2			P	HPO:probinson[2021-09-05];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001344	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001063	OMIM:225750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002352	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0200149	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001263	PMID:17357087	PCS	HP:0003593	1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001263	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002071	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0007352	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000007	PMID:16845398	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000967	PMID:20799324	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001257	PMID:17357087;PMID:20799324	PCS		2/2			P	HPO:probinson[2020-11-27];HPO:skoehler[2010-06-20];HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000006	OMIM:225750	IEA					I	HPO:skoehler[2012-10-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002240	PMID:17846997	TAS		9/19			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0010783	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000979	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0008872	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001945	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002910	PMID:17846997	PCS		6/19			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0007305	PMID:17357087	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0006579	OMIM:225750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001744	OMIM:225750	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0007229	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002633	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002135	PMID:17357087;PMID:20799324;PMID:16845398	PCS		25/25			P	HPO:probinson[2021-09-05];HPO:iea[2009-02-17];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0008936	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002059	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0009709	PMID:17357087;PMID:17846997;PMID:16845398	PCS		34/34			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0004394	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000821	PMID:25604658	PCS		6/79			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001638	PMID:25604658	PCS		9/79			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0009710	PMID:17357087;PMID:25604658;PMID:16845398	PCS		40/90			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0003613	PMID:25604658	PCS		1/79			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0002448	OMIM:225750	IEA					P	HPO:iea[2009-02-17]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0001873	PMID:17846997	PCS		12/17			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000501	PMID:25604658	PCS		7/79			P	HPO:probinson[2020-11-27]
OMIM:225750	Aicardi-Goutieres syndrome 1		HP:0000742	PMID:20799324	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:268650	Rudiger syndrome		HP:0000054	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0000023	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0001371	OMIM:268650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268650	Rudiger syndrome		HP:0001042	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0011927	OMIM:268650	TAS					P	HPO:probinson[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0000280	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0005280	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0001804	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0001609	OMIM:268650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268650	Rudiger syndrome		HP:0011220	OMIM:268650	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268650	Rudiger syndrome		HP:0000954	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0000007	OMIM:268650	IEA					I	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0000813	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0001522	OMIM:268650	IEA					C	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0002007	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0000138	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:268650	Rudiger syndrome		HP:0008714	OMIM:268650	IEA					P	HPO:iea[2009-02-17]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0004523	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0007835	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0001792	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0004322	OMIM:201180	TAS		HP:0040280			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0001250	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0008807	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0010049	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0009882	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000316	OMIM:201180	TAS		HP:0040280			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000337	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000410	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000677	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0001249	OMIM:201180	TAS		HP:0040280			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0001089	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000154	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000175	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000431	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000272	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0011304	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000508	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000767	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000349	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000568	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000007	OMIM:201180	TAS					I	HPO:skoehler[2015-12-30]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000527	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000648	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000303	OMIM:201180	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000248	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:201180	Acrofrontofacionasal dysostosis 1		HP:0000204	OMIM:201180	TAS					P	HPO:skoehler[2015-11-15]
OMIM:619538	Cerebral cavernous malformations 4		HP:0025352	PMID:34496175	PCS					I	HPO:probinson[2022-01-23]
OMIM:619538	Cerebral cavernous malformations 4		HP:0033522	PMID:34496175	PCS					P	HPO:probinson[2022-01-23]
OMIM:619538	Cerebral cavernous malformations 4		HP:0000006	PMID:34496175	PCS					I	HPO:probinson[2022-09-04]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0003378	PMID:11743580	PCS		0/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0003577	PMID:12821518	PCS		3/9			C	HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0003431	PMID:11743580	PCS				HP:0012825	P	HPO:probinson[2012-03-12];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0001761	PMID:12821518	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0001178	PMID:12821518	PCS		3/9			P	HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0006937	PMID:12821518	PCS		9/9			P	HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0001371	PMID:12821518	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0003693	PMID:11743580	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0003383	PMID:12821518	PCS		2/2			P	HPO:probinson[2012-03-12];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0002460	PMID:11743580	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0001284	PMID:12821518	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0003380	PMID:12821518	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0007230	PMID:11743580	PCS					P	HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0011463	PMID:12821518	PCS		6/9			C	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0001609	PMID:12821518	PCS		6/9			P	HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0008443	PMID:12821518	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0000007	PMID:11743580	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0001604	PMID:11743580	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0006886	PMID:12821518	PCS		9/9			P	HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0000764	PMID:11743580	PCS					P	HPO:probinson[2022-09-22]
OMIM:607706	Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomalrecessive		HP:0007328	PMID:12821518	PCS		9/9			P	HPO:probinson[2022-09-22]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0002421	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000341	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0002169	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0002521	PMID:34172529	PCS		2/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0001250	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0030674	PMID:34172529	PCS		1/2			C	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0010808	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0001252	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0001274	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0003593	PMID:36553519;PMID:34172529	PCS		2/3			C	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000283	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0032794	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0001290	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0012704	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0012444	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0033725	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0012469	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000639	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0001508	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000737	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0020221	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000637	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0002119	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0002019	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000212	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0001347	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0002179	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0030842	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0030048	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0011968	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0005484	PMID:34172529	PCS		2/2			P	HPO:probinson[2023-06-14];HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0033454	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0011344	PMID:34172529	PCS		2/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0034295	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0034353	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0031165	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000007	PMID:36553519	PCS					I	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000648	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0007874	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0000369	PMID:36553519	PCS		1/1			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0004305	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:620352	Developmental and epileptic encephalopathy 31B, autosomal recessive		HP:0001336	PMID:34172529	PCS		1/2			P	HPO:probinson[2023-06-14]
OMIM:600082	Prostatic hyperplasia, benign		HP:0003593	OMIM:600082	IEA					C	HPO:iea[2009-02-17]
OMIM:600082	Prostatic hyperplasia, benign		HP:0008711	OMIM:600082	IEA					P	HPO:iea[2009-02-17]
OMIM:600082	Prostatic hyperplasia, benign		HP:0000006	OMIM:600082	IEA					I	HPO:iea[2009-02-17]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001298	PMID:32004445	PCS	HP:0003623	2/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0007957	PMID:32004445	PCS	HP:0003577	5/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0000054	PMID:32004445	PCS	HP:0003577	1/3	MALE		P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0002353	PMID:32004445	PCS	HP:0003623	2/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001662	PMID:32004445	PCS	HP:0003623	5/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001250	PMID:32004445	PCS	HP:0003623	2/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001371	PMID:32004445	PCS	HP:0003577	2/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001639	PMID:32004445	PCS	HP:0003577	3/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0000519	PMID:32004445	PCS	HP:0003577	1/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001789	PMID:32004445	PCS	HP:0011461	2/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001319	PMID:32004445	PCS	HP:0003623	5/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001989	PMID:32004445	PCS	HP:0011461	1/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001522	PMID:32004445	PCS		5/5			C	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0000047	PMID:32004445	PCS	HP:0003577	1/3	MALE		P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0000006	PMID:32004445	PCS					I	HPO:probinson[2020-06-09];HPO:probinson[2022-12-03]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0000028	PMID:32004445	PCS	HP:0003577	1/3	MALE		P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0002500	PMID:32004445	PCS					P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0003128	PMID:32004445	PCS	HP:0003623	3/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0001644	PMID:32004445	PCS	HP:0003577	2/5			P	HPO:probinson[2020-06-09]
OMIM:618815	Chromosome 1p36.33 duplication syndrome, ATAD3 gene cluster		HP:0009879	PMID:32004445	PCS	HP:0003577	1/5			P	HPO:probinson[2020-06-09]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0000275	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0003510	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0007605	OMIM:210700	TAS					P	HPO:probinson[2012-03-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0002293	OMIM:210700	TAS					P	HPO:skoehler[2013-06-05]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0001090	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0000508	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0000007	OMIM:210700	IEA					I	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0006872	PMID:5458566	PCS					P	HP:probinson[2019-02-18]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0000444	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0002216	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0000278	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0000028	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:210700	Microcephalic primordial dwarfism, Montreal type		HP:0001249	OMIM:210700	IEA					P	HPO:iea[2009-02-17]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0000175	OMIM:300261	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0000486	OMIM:300261	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0001773	OMIM:300261	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0004322	OMIM:300261	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0001250	OMIM:300261	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0000272	OMIM:300261	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0011800	OMIM:300261	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0000518	OMIM:300261	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0001419	PMID:10398235	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2020-08-09]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0011220	OMIM:300261	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0001417	OMIM:300261	TAS					I	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0200055	OMIM:300261	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0000501	OMIM:300261	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0001249	OMIM:300261	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300261	Intellectual developmental disorder, X-linked syndromic, Armfield type		HP:0005922	OMIM:300261	TAS					P	HPO:skoehler[2012-10-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0002059	PMID:25466870	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0003621	PMID:25466870	PCS		2/5			C	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0003431	PMID:25466870	PCS		5/5			P	HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0004322	PMID:25466870	PCS		4/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0003487	PMID:25466870	PCS		2/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0001272	PMID:25466870	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0002066	PMID:25466870	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0010871	PMID:25466870	PCS		5/5			P	HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0100651	PMID:25466870	PCS		5/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0034063	PMID:25466870	PCS		0/5			P	HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0100543	PMID:25466870	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0025708	PMID:25466870	PCS		1/5			C	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0000407	PMID:25466870	PCS		5/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0011463	PMID:25466870	PCS		2/5			C	HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0009830	PMID:25466870	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0000007	PMID:25466870	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0007366	OMIM:616192	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0040217	PMID:25466870	PCS		5/5			P	HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0003448	PMID:25466870	PCS		5/5			P	HPO:probinson[2022-05-14]
OMIM:616192	Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus		HP:0002522	PMID:25466870	PCS		3/5			P	HPO:probinson[2022-05-14]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0001342	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0003345	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0003574	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0001095	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0000093	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0003072	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0000957	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0000975	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0000997	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0001635	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0001649	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0000006	OMIM:171420	IEA					I	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0000875	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:171420	Pheochromocytoma-Islet cell tumor syndrome		HP:0002666	OMIM:171420	IEA					P	HPO:iea[2009-02-17]
OMIM:605850	Dimethylglycine dehydrogenase deficiency		HP:0003236	PMID:10102904	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:605850	Dimethylglycine dehydrogenase deficiency		HP:0031945	PMID:10102904	PCS					P	HP:probinson[2019-01-22]
OMIM:605850	Dimethylglycine dehydrogenase deficiency		HP:0003750	PMID:10102904	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:605850	Dimethylglycine dehydrogenase deficiency		HP:0031946	PMID:10102904	PCS					P	HP:probinson[2019-01-22]
OMIM:605850	Dimethylglycine dehydrogenase deficiency		HP:0410020	PMID:10102904	PCS					P	HP:probinson[2019-01-22]
OMIM:605850	Dimethylglycine dehydrogenase deficiency		HP:0000007	PMID:10102904	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-01-22]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0001289	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0003596	PMID:2563037	PCS					C	HPO:probinson[2022-06-24]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0002354	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0002066	OMIM:123400	TAS					P	HPO:probinson[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0002381	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000716	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000738	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000726	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0007076	OMIM:123400	TAS					P	HPO:probinson[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000737	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000605	OMIM:123400	TAS					P	HPO:probinson[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000739	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0001317	OMIM:123400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0002922	OMIM:123400	TAS		HP:0040283		HP:0012825	P	HPO:iea[2015-02-01]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000505	OMIM:123400	TAS					P	HPO:probinson[2015-02-01]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000746	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000741	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0001269	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000751	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0000006	PMID:2563037	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-06-24]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0005327	OMIM:123400	TAS					P	HPO:probinson[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0001336	OMIM:123400	TAS					P	HPO:iea[2009-02-17]
OMIM:123400	Creutzfeldt-Jakob disease		HP:0003678	OMIM:123400	TAS					C	HPO:iea[2009-02-17]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0025671	PMID:25557780	PCS	HP:0011461	1/6			P	HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0001561	OMIM:219730	TAS					P	HPO:skoehler[2012-10-17]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0001250	PMID:25557780	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0000083	OMIM:219730	TAS					P	HPO:skoehler[2015-04-05]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0002282	PMID:25557780	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0011432	PMID:25557780	PCS		6/6			H	HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0032622	PMID:25557780	PCS		1/5			P	HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0100259	OMIM:219730	TAS					P	HPO:skoehler[2015-12-30]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0001629	PMID:25557780	PCS		1/6			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0011461	PMID:25557780	PCS		6/6			C	HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0004719	PMID:25557780	PCS		2/6			P	HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0000007	PMID:25557780	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0000238	OMIM:219730	IEA					P	HPO:iea[2009-02-17]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0002617	OMIM:219730	IEA					P	HPO:skoehler[2018-10-08]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0002119	PMID:25557780	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0000108	PMID:25557780	PCS	HP:0011461	4/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-11]
OMIM:219730	Ventriculomegaly with cystic kidney disease		HP:0001622	OMIM:219730	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0002366	PMID:21145000	PCS					P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003236	PMID:21145000	PCS		2/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003596	PMID:21145000	PCS					C	HPO:probinson[2020-07-22]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0002061	PMID:21145000	PCS		1/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0002380	OMIM:613954	IEA		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003690	PMID:21145000	PCS		1/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0000716	PMID:21145000	PCS					P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0007340	PMID:21145000	PCS		1/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0002878	PMID:21145000	PCS					P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003803	PMID:21145000	PCS		1/1			P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0001324	PMID:21145000	PCS		9/9			P	HPO:probinson[2013-08-10];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0000751	PMID:21145000	PCS		1/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0001348	PMID:21145000	PCS		5/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003202	PMID:21145000	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003444	PMID:21145000	PCS		4/4			P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0002015	PMID:21145000	PCS					P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0001288	PMID:21145000	PCS		1/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003487	PMID:21145000	PCS		3/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0001260	PMID:21145000	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0002273	PMID:21145000	PCS					P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0011448	PMID:21145000	PCS		1/9			P	HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0007354	PMID:21145000	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-22]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0001257	PMID:21145000	PCS					P	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0000006	PMID:21145000	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-22]
OMIM:613954	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6		HP:0003557	PMID:21145000	PCS		1/9			P	HPO:probinson[2022-02-04]
OMIM:310700	Nystagmus 1, congenital, X-linked		HP:0006934	OMIM:310700	IEA					P	HPO:iea[2009-02-17]
OMIM:310700	Nystagmus 1, congenital, X-linked		HP:0003593	OMIM:310700	IEA					C	HPO:iea[2009-02-17]
OMIM:310700	Nystagmus 1, congenital, X-linked		HP:0012043	OMIM:310700	TAS					P	HPO:probinson[2012-08-01]
OMIM:310700	Nystagmus 1, congenital, X-linked		HP:0007663	OMIM:310700	TAS				HP:0012825	P	HPO:probinson[2015-07-20]
OMIM:310700	Nystagmus 1, congenital, X-linked		HP:0032037	OMIM:310700	IEA					P	HPO:skoehler[2019-02-22]
OMIM:310700	Nystagmus 1, congenital, X-linked		HP:0001417	PMID:17013395	PCS					I	HPO:probinson[2022-09-02]
OMIM:310700	Nystagmus 1, congenital, X-linked		HP:0000666	OMIM:310700	IEA					P	HPO:iea[2009-02-17]
OMIM:607921	Retinitis pigmentosa 30		HP:0007737	PMID:11527955	PCS					P	HPO:probinson[2013-03-04]
OMIM:607921	Retinitis pigmentosa 30		HP:0000662	PMID:11527955	PCS	HP:0011463				P	HPO:probinson[2013-03-04]
OMIM:607921	Retinitis pigmentosa 30		HP:0000505	PMID:11527955	PCS					P	HPO:probinson[2013-03-04]
OMIM:607921	Retinitis pigmentosa 30		HP:0000648	PMID:11527955	PCS					P	HPO:probinson[2013-03-04]
OMIM:607921	Retinitis pigmentosa 30		HP:0000510	PMID:11527955	PCS					P	HPO:probinson[2013-03-04]
OMIM:607921	Retinitis pigmentosa 30		HP:0007843	PMID:11527955	PCS					P	HPO:probinson[2013-03-04]
OMIM:607921	Retinitis pigmentosa 30		HP:0000006	PMID:11527955	PCS					I	HPO:probinson[2013-01-09]
OMIM:607921	Retinitis pigmentosa 30		HP:0000533	PMID:11527955	PCS					P	HPO:probinson[2013-03-04]
OMIM:618801	Ciliary dyskinesia, primary, 45		HP:0002257	PMID:31978331	PCS					P	HPO:probinson[2020-06-09]
OMIM:618801	Ciliary dyskinesia, primary, 45		HP:0002110	PMID:31978331	PCS		2/4			P	HPO:probinson[2020-06-09]
OMIM:618801	Ciliary dyskinesia, primary, 45		HP:0003251	PMID:31978331	PCS		2/2	MALE		P	HPO:probinson[2020-06-09];HPO:probinson[2020-06-09]
OMIM:618801	Ciliary dyskinesia, primary, 45		HP:0012263	PMID:31978331	PCS					P	HPO:probinson[2020-06-09]
OMIM:618801	Ciliary dyskinesia, primary, 45		HP:0000007	PMID:31978331	PCS					I	HPO:probinson[2020-06-09];HPO:probinson[2020-06-09]
OMIM:618801	Ciliary dyskinesia, primary, 45		HP:0002205	PMID:31978331	PCS					P	HPO:probinson[2020-06-09]
OMIM:618801	Ciliary dyskinesia, primary, 45		HP:0012259	PMID:31978331	PCS					P	HPO:probinson[2020-06-09]
OMIM:127100	Dwarfism, Levi type		HP:0003510	OMIM:127100	IEA					P	HPO:iea[2009-02-17]
OMIM:127100	Dwarfism, Levi type		HP:0000271	OMIM:127100	IEA					P	HPO:iea[2009-02-17]
OMIM:127100	Dwarfism, Levi type		HP:0001518	OMIM:127100	IEA					P	HPO:iea[2009-02-17]
OMIM:127100	Dwarfism, Levi type		HP:0000007	OMIM:127100	IEA					I	HPO:iea[2009-02-17]
OMIM:127100	Dwarfism, Levi type		HP:0000006	OMIM:127100	IEA					I	HPO:iea[2009-02-17]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002069	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0000750	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0001310	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0001332	PMID:32383294	PCS		2/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002066	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0001252	PMID:32383294	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002151	PMID:32383294	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002063	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0003593	PMID:32383294	PCS		2/2			C	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002194	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0001270	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0003819	OMIM:203740	TAS					C	HPO:probinson[2009-02-17]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0000007	PMID:32383294	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002317	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002119	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0004902	OMIM:203740	IEA					P	HPO:iea[2009-02-17]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0002527	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0001942	OMIM:203740	IEA					P	HPO:iea[2009-02-17]
OMIM:203740	Oxoglutarate dehydrogenase deficiency		HP:0003700	PMID:32383294	PCS		1/2			P	HPO:probinson[2022-03-27]
OMIM:609924	Aminoacylase 1 deficiency		HP:0002069	PMID:16274666	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:609924	Aminoacylase 1 deficiency		HP:0006846	PMID:16274666	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:609924	Aminoacylase 1 deficiency		HP:0002059	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0002188	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0000431	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001662	PMID:16274666	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001272	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0002120	PMID:16274666	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:609924	Aminoacylase 1 deficiency		HP:0011968	PMID:16274666	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001250	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001263	OMIM:609924	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001252	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001290	PMID:16274666	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:609924	Aminoacylase 1 deficiency		HP:0000407	PMID:16274666	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0000316	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0000007	PMID:16274666	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:609924	Aminoacylase 1 deficiency		HP:0000752	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001324	OMIM:609924	IEA					P	HPO:iea[2009-02-17]
OMIM:609924	Aminoacylase 1 deficiency		HP:0001623	PMID:16274666	PCS		1/1			P	HPO:probinson[2023-04-02]
OMIM:609924	Aminoacylase 1 deficiency		HP:0003623	PMID:16274666	PCS		1/1			C	HPO:probinson[2023-04-02]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0002003	PMID:32109420	PCS		3/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001531	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000486	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000463	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001332	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001250	PMID:32109420	PCS		2/4			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0002020	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0004383	PMID:32109420	PCS	HP:0030674	1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001270	PMID:32109420	PCS		5/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0045075	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0012450	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0008551	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000316	PMID:32109420	PCS		4/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000414	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0008872	PMID:32109420	PCS	HP:0003623	2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000637	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000218	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001269	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000411	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001249	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000358	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001561	PMID:32109420	IEA	HP:0011461	1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000750	PMID:32109420	PCS		4/4			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000233	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0031936	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0002076	PMID:32109420	PCS		3/10			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000490	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0002072	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001182	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0005280	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0010535	PMID:32109420	PCS		3/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0100336	PMID:32109420	PCS		1/5			P	HPO:probinson[2024-03-08]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0100337	PMID:32109420	PCS		1/5			P	HPO:probinson[2024-03-08]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000426	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000448	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000821	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0001319	PMID:32109420	PCS	HP:0003623	2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000307	PMID:32109420	PCS		2/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0004209	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0002007	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000003	PMID:32109420	PCS	HP:0003577	1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000006	PMID:32109420	PCS					I	HPO:probinson[2020-08-15];HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000369	PMID:32109420	PCS		3/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000347	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618829	Nabais Sa-de vries syndrome, type 2		HP:0000325	PMID:32109420	PCS		1/5			P	HPO:probinson[2020-08-15]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0001265	PMID:26870663	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0030205	PMID:26870663	PCS		2/2			P	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0031936	OMIM:618197	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0003388	PMID:26870663	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0001761	PMID:26870663	PCS		1/3			P	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0001283	PMID:26870663	PCS		1/3			P	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0003473	PMID:26870663	PCS		3/3			P	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0002033	PMID:26870663	PCS		1/3			P	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0001263	PMID:26870663	PCS		2/3			P	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0001274	PMID:26870663	PCS		1/3			P	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0003593	PMID:26870663	PCS		2/3			C	HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0001270	OMIM:618197	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0008981	PMID:26870663	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0000508	PMID:26870663	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0000007	PMID:26870663	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-11]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0002359	OMIM:618197	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0001324	OMIM:618197	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0000467	OMIM:618197	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618197	Myasthenic syndrome, congenital, 23, presynaptic		HP:0003623	PMID:26870663	PCS		1/3			C	HPO:probinson[2022-12-11]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0003510	OMIM:126550	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0000670	PMID:11241496	PCS					P	HPO:iea[2015-03-22]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0002980	OMIM:126550	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0002650	OMIM:126550	IEA					P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0002684	OMIM:126550	IEA					P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0003155	PMID:11241496	PCS					P	HPO:iea[2015-03-22]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0001270	OMIM:126550	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0000939	OMIM:126550	IEA					P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0000938	OMIM:126550	IEA					P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0000926	OMIM:126550	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0002757	PMID:11241496	PCS					P	HPO:iea[2015-03-22]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0000410	OMIM:126550	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:126550	Calvarial doughnut lesions with bone fragility		HP:0000006	PMID:11241496	PCS					I	HPO:iea[2009-02-17]
OMIM:151900	Lipomatosis, multiple		HP:0001012	OMIM:151900	TAS					P	HPO:skoehler[2010-06-20]
OMIM:151900	Lipomatosis, multiple		HP:0000006	OMIM:151900	TAS					I	HPO:iea[2009-02-17]
OMIM:103920	Allergic bronchopulmonary aspergillosis		HP:0002715	OMIM:103920	IEA					P	HPO:iea[2009-02-17]
OMIM:103920	Allergic bronchopulmonary aspergillosis		HP:0000006	OMIM:103920	IEA					I	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0002663	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000286	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002982	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0003038	PMID:12161603	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002980	OMIM:114290	TAS				HP:0012825	P	HPO:probinson[2015-03-01]
OMIM:114290	Campomelic dysplasia		HP:0000365	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0000882	PMID:12161603	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0006628	OMIM:114290	TAS					P	HPO:probinson[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0002783	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0005257	OMIM:114290	TAS					P	HPO:probinson[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0001250	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000160	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001252	PMID:12161603	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0004482	PMID:12161603	PCS		3/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0012745	OMIM:114290	TAS					P	HPO:skoehler[2014-03-24]
OMIM:114290	Campomelic dysplasia		HP:0010646	PMID:16555077	PCS		1/1			P	HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0006390	PMID:12161603	PCS		1/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0011343	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0011342	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000316	PMID:12161603	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000238	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0002779	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000878	PMID:12161603	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002414	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001840	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001763	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002751	PMID:12161603	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000176	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000175	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0011968	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001382	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001263	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0011800	PMID:16555077	PCS		1/1			P	HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0003083	PMID:12161603	PCS		2/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002827	PMID:12161603	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002947	PMID:16555077	PCS		1/1			P	HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0009697	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000405	PMID:12161603	PCS		3/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002868	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000768	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0008921	PMID:12161603	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002788	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002866	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0000047	PMID:16555077	PCS		1/1			P	HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0000883	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0002943	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002104	PMID:12161603	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000006	PMID:12161603	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000369	PMID:12161603;PMID:16555077	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31];HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0002786	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0001776	PMID:12161603;PMID:16555077	PCS		3/6			P	HPO:probinson[2022-03-31];HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0000126	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0032538	PMID:12161603;PMID:16555077	PCS		3/6			P	HPO:probinson[2022-03-31];HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0003577	PMID:12161603	PCS		5/5			C	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000343	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0010307	PMID:12161603	PCS		2/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0030674	PMID:16555077	IEA		1/1			C	HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0000260	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0005035	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0000581	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0011910	OMIM:114290	IEA					P	HPO:iea[2012-06-09]
OMIM:114290	Campomelic dysplasia		HP:0010301	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0012368	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001508	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0010034	PMID:12161603	PCS		2/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0040079	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0008873	PMID:12161603	PCS	HP:0003577				P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0008477	OMIM:114290	TAS					P	HPO:probinson[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0001822	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001627	OMIM:114290	TAS					P	HPO:skoehler[2015-12-30]
OMIM:114290	Campomelic dysplasia		HP:0000218	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0008434	OMIM:114290	TAS					P	HPO:probinson[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0000256	PMID:12161603	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:114290	Campomelic dysplasia		HP:0000457	OMIM:114290	TAS					P	HPO:probinson[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0009803	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0003026	PMID:12161603	PCS		2/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000670	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001561	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0000274	OMIM:114290	IEA					P	HPO:skoehler[2010-06-20]
OMIM:114290	Campomelic dysplasia		HP:0002650	PMID:12161603	PCS		3/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001762	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0002098	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0003065	PMID:12161603	PCS		3/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0005280	PMID:12161603	PCS		5/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0012245	PMID:12161603	PCS		1/5			P	HPO:probinson[2013-04-02];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000348	OMIM:114290	IEA					P	HPO:iea[2009-02-17]
OMIM:114290	Campomelic dysplasia		HP:0006487	PMID:12161603	PCS		3/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002007	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000347	PMID:12161603	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0000545	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0002643	PMID:12161603	PCS		3/5			P	HPO:probinson[2022-03-31]
OMIM:114290	Campomelic dysplasia		HP:0001799	PMID:12161603	PCS		1/5			P	HPO:probinson[2022-03-31]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002465	PMID:23023333	PCS					P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000483	PMID:23023333	PCS		2/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0010804	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0004684	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002066	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001252	PMID:23023333	PCS		2/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002020	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0003593	PMID:23023333	PCS		4/6			C	HPO:probinson[2022-10-23];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001290	PMID:23023333	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000998	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0020045	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002019	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001249	PMID:23023333	PCS					P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000358	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001344	PMID:23023333	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000574	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002079	PMID:23023333	PCS		5/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001387	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0011968	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001263	PMID:23023333	PCS		6/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002072	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000007	PMID:23023333	PCS					I	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000527	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000565	PMID:23023333	PCS		2/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001257	PMID:23023333	PCS		1/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000369	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001655	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001276	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0003577	PMID:23023333	PCS		2/6			C	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000463	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000540	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002365	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001629	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0100704	PMID:23023333	PCS		2/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001348	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001347	PMID:23023333	PCS		2/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0008936	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002015	PMID:23023333	PCS					P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002650	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001762	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001321	PMID:23023333	PCS		5/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0031936	PMID:23023333	PCS		3/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002376	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0001761	OMIM:614961	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0005484	PMID:23023333	PCS		1/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0012760	PMID:23023333	PCS		4/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0034295	PMID:23023333	PCS		6/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0002804	PMID:23023333	PCS		2/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000664	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0004305	PMID:23023333	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:614961	Pontocerebellar hypoplasia, type 8		HP:0000545	PMID:23023333	PCS		1/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-10-23]
OMIM:611819	Long QT syndrome 10		HP:0003621	PMID:17592081	PCS		1/3			C	HPO:probinson[2022-07-09]
OMIM:611819	Long QT syndrome 10		HP:0012266	PMID:17592081	PCS					P	HPO:probinson[2013-04-07]
OMIM:611819	Long QT syndrome 10		HP:0011463	PMID:17592081	PCS		1/3			C	HPO:probinson[2022-07-09]
OMIM:611819	Long QT syndrome 10		HP:0003581	PMID:17592081	PCS		1/3			C	HPO:probinson[2022-07-09]
OMIM:611819	Long QT syndrome 10		HP:0005110	OMIM:611819	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:611819	Long QT syndrome 10		HP:0001657	PMID:17592081	PCS					P	HPO:probinson[2013-01-09]
OMIM:611819	Long QT syndrome 10		HP:0000006	PMID:17592081	PCS					I	HPO:probinson[2013-04-03]
OMIM:611819	Long QT syndrome 10		HP:0001645	PMID:17592081	PCS		2/10			P	HPO:probinson[2013-04-03];HPO:probinson[2022-07-09]
OMIM:611819	Long QT syndrome 10		HP:0001678	PMID:17592081	PCS					P	HPO:probinson[2013-04-03]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002202	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002243	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0003073	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002917	OMIM:618183	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0012050	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0001522	PMID:26207260	PCS		1/1			C	HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0005208	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0001942	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0003623	PMID:26207260	PCS		1/1			C	HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000110	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0004313	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0001561	OMIM:618183	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002573	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002155	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0001541	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0011968	PMID:26207260	PCS		1/1			P	HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002902	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000007	PMID:26207260	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000821	OMIM:618183	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002925	PMID:26207260	PCS		1/1			P	HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002901	OMIM:618183	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0001698	OMIM:618183	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000103	OMIM:618183	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0002788	PMID:26207260	PCS		1/1			P	HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000028	PMID:26207260	PCS		1/1	MALE		P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000369	PMID:26207260	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000347	PMID:26207260	PCS		1/1			P	HPO:probinson[2023-02-16]
OMIM:618183	Diarrhea 10, protein-losing enteropathy type		HP:0000589	PMID:26207260	PCS		1/1			P	HPO:probinson[2023-02-16]
OMIM:608390	Myotonia, potassium-aggravated		HP:0003202	PMID:9771789	PCS		1/2			P	HPO:probinson[2022-12-12]
OMIM:608390	Myotonia, potassium-aggravated		HP:0003236	OMIM:608390	TAS		HP:0040283			P	HPO:probinson[2013-03-11]
OMIM:608390	Myotonia, potassium-aggravated		HP:0003552	OMIM:608390	IEA					P	HPO:skoehler[2012-10-17]
OMIM:608390	Myotonia, potassium-aggravated		HP:0010307	OMIM:608390	IEA					P	HPO:skoehler[2012-10-17]
OMIM:608390	Myotonia, potassium-aggravated		HP:0002486	PMID:9771789	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-12]
OMIM:608390	Myotonia, potassium-aggravated		HP:0012899	PMID:9771789	PCS		1/2			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:608390	Myotonia, potassium-aggravated		HP:0010548	PMID:9771789	PCS		2/2			P	HPO:probinson[2022-12-12]
OMIM:608390	Myotonia, potassium-aggravated		HP:0011462	PMID:9771789	PCS		1/2			C	HPO:probinson[2022-12-12]
OMIM:608390	Myotonia, potassium-aggravated		HP:0005949	OMIM:608390	TAS					P	HPO:skoehler[2013-01-22]
OMIM:608390	Myotonia, potassium-aggravated		HP:0025425	OMIM:608390	TAS	HP:0003623				P	HPO:skoehler[2017-07-13]
OMIM:608390	Myotonia, potassium-aggravated		HP:0003712	OMIM:608390	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608390	Myotonia, potassium-aggravated		HP:0001324	PMID:9771789	PCS		0/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-12]
OMIM:608390	Myotonia, potassium-aggravated		HP:0000006	PMID:9771789	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:608390	Myotonia, potassium-aggravated		HP:0003326	OMIM:608390	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608390	Myotonia, potassium-aggravated		HP:0003623	PMID:9771789	PCS		1/2			C	HPO:probinson[2022-12-12]
OMIM:211350	Kyphomelic dysplasia		HP:0002982	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0003015	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0002983	OMIM:211350	TAS				HP:0012828	P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0002980	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0001376	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0003498	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0005257	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0003031	PMID:11140840	PCS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0003097	OMIM:211350	TAS					P	HPO:probinson[2012-06-10]
OMIM:211350	Kyphomelic dysplasia		HP:0005792	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0010049	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0012368	OMIM:211350	TAS					P	HPO:skoehler[2013-10-22]
OMIM:211350	Kyphomelic dysplasia		HP:0000895	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0005009	OMIM:211350	TAS					P	HPO:probinson[2012-06-10]
OMIM:211350	Kyphomelic dysplasia		HP:0003865	PMID:11140840	PCS					P	HPO:probinson[2015-03-01]
OMIM:211350	Kyphomelic dysplasia		HP:0000175	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0001762	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0005280	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0003180	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0000907	OMIM:211350	TAS					P	HPO:probinson[2012-06-10]
OMIM:211350	Kyphomelic dysplasia		HP:0010561	OMIM:211350	TAS					P	HPO:probinson[2012-06-10]
OMIM:211350	Kyphomelic dysplasia		HP:0000926	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0000007	OMIM:211350	TAS					I	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0000348	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0002986	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0001059	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0000204	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0000347	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:211350	Kyphomelic dysplasia		HP:0000369	OMIM:211350	TAS					P	HPO:probinson[2009-02-17]
OMIM:611818	Long QT syndrome 9		HP:0003621	PMID:17060380	PCS		4/6			C	HPO:probinson[2022-06-03]
OMIM:611818	Long QT syndrome 9		HP:0001695	PMID:17060380	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:611818	Long QT syndrome 9		HP:0025070	PMID:17060380	PCS		1/6			P	HPO:probinson[2022-06-03]
OMIM:611818	Long QT syndrome 9		HP:0001657	PMID:17060380	PCS		6/6			P	HPO:probinson[2013-01-09];HPO:probinson[2022-06-03]
OMIM:611818	Long QT syndrome 9		HP:0100749	PMID:17060380	PCS		1/6			P	HPO:probinson[2022-06-03]
OMIM:611818	Long QT syndrome 9		HP:0004308	PMID:17060380	PCS					P	HPO:probinson[2013-04-03]
OMIM:611818	Long QT syndrome 9		HP:0025710	PMID:17060380	PCS		2/6			C	HPO:probinson[2022-06-03]
OMIM:611818	Long QT syndrome 9		HP:0001279	PMID:17060380	PCS		3/6			P	HPO:probinson[2022-06-03]
OMIM:611818	Long QT syndrome 9		HP:0000006	PMID:17060380	PCS					I	HPO:probinson[2013-04-03]
OMIM:611818	Long QT syndrome 9		HP:0001688	PMID:17060380	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:618182	Orthostatic hypotension 2		HP:0001278	PMID:29343526	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618182	Orthostatic hypotension 2		HP:0001903	PMID:29343526	PCS		2/2		HP:0012825	P	HPO:probinson[2022-05-31]
OMIM:618182	Orthostatic hypotension 2		HP:0011463	PMID:29343526	PCS		2/4			C	HPO:probinson[2022-05-31]
OMIM:618182	Orthostatic hypotension 2		HP:0003593	PMID:29343526	PCS		2/4			C	HPO:probinson[2022-05-31]
OMIM:618182	Orthostatic hypotension 2		HP:0000007	PMID:29343526	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-31]
OMIM:618182	Orthostatic hypotension 2		HP:0001943	PMID:29343526	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-31]
OMIM:618182	Orthostatic hypotension 2		HP:0012213	PMID:29343526	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-31]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0000011	PMID:32715519	PCS		1/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0001265	PMID:32715519	PCS					P	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0001761	PMID:32715519	PCS		37/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0001288	PMID:32715519	PCS					P	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0008959	PMID:32715519	PCS		10/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0003487	PMID:32715519	PCS		28/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0011924	PMID:32715519	PCS		2/3			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0002495	PMID:32715519	PCS		26/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0033686	PMID:29062908	PCS		2/2			P	HPO:probinson[2021-04-16]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0003393	PMID:32715519	PCS		10/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0033685	PMID:32715519	PCS		4/4			P	HPO:probinson[2021-04-16]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0010871	PMID:32715519	PCS		42/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0011923	PMID:32715519	PCS		2/3			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0010831	PMID:32715519	PCS		23/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0007181	PMID:32715519	PCS		10/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0009053	PMID:32715519	PCS					P	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0008110	PMID:32715519	PCS		5/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0007141	PMID:32715519	PCS					P	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0001427	PMID:32715519	PCS					I	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0008347	PMID:32715519	PCS		2/3			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0002313	PMID:32715519	PCS		5/44			P	HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0008944	PMID:32715519	PCS					P	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:500013	Mitochondrial form of axonal Charcot-Marie-Tooth disease-1		HP:0001347	PMID:32715519	PCS					P	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:241200	Bartter syndrome, type 2		HP:0003158	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000121	PMID:8841184	PCS		7/8			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0003113	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0004322	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001250	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0003394	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001090	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0011220	OMIM:241200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002019	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001249	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0003623	PMID:8841184	PCS		9/9			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0003324	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0003566	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0003401	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001263	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002150	PMID:8841184	PCS		9/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0003081	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000848	PMID:8841184	PCS		9/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0000007	PMID:8841184	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0000128	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002900	PMID:8841184	PCS		9/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0000400	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000127	OMIM:241200	TAS					P	HPO:skoehler[2013-10-06]
OMIM:241200	Bartter syndrome, type 2		HP:0000325	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000841	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001508	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000859	PMID:8841184	PCS		9/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0002917	OMIM:241200	IEA		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000938	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001944	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002914	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000934	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0003527	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001945	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000256	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002632	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001622	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002014	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001561	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001960	PMID:8841184	PCS		9/9			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:241200	Bartter syndrome, type 2		HP:0001563	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000111	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002013	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0003540	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001281	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001959	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0001518	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0002007	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:241200	Bartter syndrome, type 2		HP:0000103	OMIM:241200	IEA					P	HPO:skoehler[2009-02-17]
OMIM:208600	Asthma, short stature, and elevated iga		HP:0004322	OMIM:208600	IEA					P	HPO:iea[2009-02-17]
OMIM:208600	Asthma, short stature, and elevated iga		HP:0002099	OMIM:208600	IEA					P	HPO:iea[2009-02-17]
OMIM:208600	Asthma, short stature, and elevated iga		HP:0000007	OMIM:208600	IEA					I	HPO:iea[2009-02-17]
OMIM:208600	Asthma, short stature, and elevated iga		HP:0003261	OMIM:208600	IEA					P	HPO:iea[2009-02-17]
OMIM:613969	Myopia 19, autosomal dominant		HP:0011003	OMIM:613969	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613969	Myopia 19, autosomal dominant		HP:0000006	OMIM:613969	TAS					I	HPO:skoehler[2012-10-17]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0003577	OMIM:616811	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0003676	OMIM:616811	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0002188	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0001332	OMIM:616811	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0001272	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0001250	PMID:26626369	PCS	HP:0011463				P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0002283	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0003593	PMID:26626369	PCS					C	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0001290	OMIM:616811	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0040078	PMID:26626369	PCS	HP:0003621				P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0002416	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0000252	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0011924	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0011968	PMID:26626369	PCS	HP:0011463				P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0002151	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0001263	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0002490	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0011923	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0011344	OMIM:616811	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0009830	PMID:26626369	PCS	HP:0003621				P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0000007	PMID:26626369	PCS					I	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0002922	PMID:26626369	PCS					P	HPO:probinson[2017-06-18]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0000648	OMIM:616811	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0000488	OMIM:616811	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0001257	OMIM:616811	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616811	Combined oxidative phosphorylation deficiency 29		HP:0001138	PMID:26626369	PCS	HP:0003621				P	HPO:probinson[2017-06-18]
OMIM:176400	Precocious puberty, central		HP:0004322	OMIM:176400	TAS	HP:0003581				P	HPO:iea[2009-02-17]
OMIM:176400	Precocious puberty, central		HP:0011969	OMIM:176400	TAS					P	HPO:iea[2015-02-22]
OMIM:176400	Precocious puberty, central		HP:0008232	OMIM:176400	TAS					P	HPO:iea[2015-02-22]
OMIM:176400	Precocious puberty, central		HP:0000821	OMIM:176400	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:176400	Precocious puberty, central		HP:0008236	OMIM:176400	TAS					P	HPO:iea[2009-02-17]
OMIM:176400	Precocious puberty, central		HP:0000006	OMIM:176400	TAS					I	HPO:iea[2009-02-17]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0001276	PMID:32109420	PCS					P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000341	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000286	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000365	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0003196	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0001270	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-08-15];HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000319	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000414	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0001249	PMID:32109420	IEA		2/2			P	HPO:probinson[2020-07-23]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0006579	PMID:32109420	PCS	HP:0003623	1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0002553	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000494	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000076	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000750	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0031936	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0002057	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000391	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000490	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0001263	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-07-23]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000294	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0045025	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0005280	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0011471	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000609	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0009891	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000506	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0011451	PMID:32109420	PCS	HP:0003577	2/2			P	HPO:probinson[2020-07-23]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000426	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0100716	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000527	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000307	PMID:32109420	PCS		2/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0004209	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000664	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000960	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000006	PMID:32109420	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0002643	PMID:32109420	IEA	HP:0003623	1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0000248	PMID:32109420	PCS		1/2			P	HPO:probinson[2020-08-15]
OMIM:618828	Nabais Sa-de Vries syndrome, type 1		HP:0009879	PMID:32109420	PCS		1/1			P	HPO:probinson[2020-08-15]
OMIM:101850	ACROKERATOELASTOIDOSIS		HP:0200016	OMIM:101850	IEA					P	HPO:iea[2009-02-17]
OMIM:101850	ACROKERATOELASTOIDOSIS		HP:0000006	OMIM:101850	IEA					I	HPO:iea[2009-02-17]
OMIM:101850	ACROKERATOELASTOIDOSIS		HP:0000962	OMIM:101850	IEA					P	HPO:iea[2009-02-17]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0001882	OMIM:231095	TAS		HP:0040283			P	HPO:skoehler[2013-02-25]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0011001	OMIM:231095	TAS					P	HPO:skoehler[2013-02-25]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0005890	OMIM:231095	TAS		12/20			P	HPO:skoehler[2009-02-17];HPO:skoehler[2013-02-23]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0000007	OMIM:231095	TAS					I	HPO:skoehler[2009-02-17]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0100252	OMIM:231095	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0005528	OMIM:231095	TAS					P	HPO:skoehler[2009-02-17]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0001873	OMIM:231095	TAS					P	HPO:skoehler[2009-02-17]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0005505	OMIM:231095	TAS					P	HPO:skoehler[2009-02-17]
OMIM:231095	Ghosal hematodiaphyseal dysplasia		HP:0011974	OMIM:231095	TAS					P	HPO:skoehler[2012-10-17]
OMIM:153870	Macular dystrophy, concentric annular		HP:0008001	OMIM:153870	TAS					P	HPO:skoehler[2009-02-17]
OMIM:153870	Macular dystrophy, concentric annular		HP:0007641	OMIM:153870	TAS					P	HPO:skoehler[2012-10-17]
OMIM:153870	Macular dystrophy, concentric annular		HP:0007754	OMIM:153870	TAS					P	HPO:skoehler[2009-02-17]
OMIM:153870	Macular dystrophy, concentric annular		HP:0000006	OMIM:153870	TAS					I	HPO:skoehler[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001254	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0000365	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0000486	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0000980	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001250	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001252	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001251	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001290	OMIM:500007	TAS					P	HPO:skoehler[2017-07-13]
OMIM:500007	Cyclic vomiting syndrome		HP:0001270	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0100543	OMIM:500007	TAS					P	HPO:skoehler[2015-12-30]
OMIM:500007	Cyclic vomiting syndrome		HP:0011463	PMID:12905015	PCS		4/4			C	HPO:probinson[2022-11-04]
OMIM:500007	Cyclic vomiting syndrome		HP:0000717	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001427	PMID:12905015	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:500007	Cyclic vomiting syndrome		HP:0001426	OMIM:500007	IEA					I	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0002579	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001324	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0002018	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001249	OMIM:500007	TAS					P	HPO:skoehler[2013-06-16]
OMIM:500007	Cyclic vomiting syndrome		HP:0002039	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0003546	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0000252	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0002013	PMID:12905015	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-04]
OMIM:500007	Cyclic vomiting syndrome		HP:0002076	PMID:12905015	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:500007	Cyclic vomiting syndrome		HP:0001638	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0007018	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0001510	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:500007	Cyclic vomiting syndrome		HP:0002027	OMIM:500007	IEA					P	HPO:iea[2009-02-17]
OMIM:614974	Focal facial dermal dysplasia 4		HP:0011336	PMID:23161670	PCS					P	HPO:probinson[2020-08-02]
OMIM:614974	Focal facial dermal dysplasia 4		HP:0000007	PMID:23161670	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2020-08-02]
OMIM:308600	Jaundice, familial obstructive, of infancy		HP:0001419	OMIM:308600	TAS					I	HPO:skoehler[2009-02-17]
OMIM:308600	Jaundice, familial obstructive, of infancy		HP:0003265	OMIM:308600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:308600	Jaundice, familial obstructive, of infancy		HP:0000952	OMIM:308600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:620409	Spermatogenic failure 84		HP:0033393	PMID:35174165	PCS		9/9			P	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0034011	PMID:35174165	PCS		10/11			P	HPO:probinson[2024-02-15];HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0032560	PMID:35174165	PCS		9/9			P	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0003251	PMID:34792097;PMID:35174165	PCS		12/12			P	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0011462	PMID:34792097;PMID:35174165	PCS		12/12			C	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0000007	PMID:34792097	PCS					I	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0012207	PMID:35174165	PCS		10/11			P	HPO:probinson[2024-02-15];HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0034811	PMID:35174165	PCS		9/9			P	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0000798	PMID:35174165	PCS		10/11			P	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0032558	PMID:35174165	PCS		9/9			P	HPO:probinson[2024-02-15]
OMIM:620409	Spermatogenic failure 84		HP:0032559	PMID:35174165	PCS		9/9			P	HPO:probinson[2024-02-15]
OMIM:618196	Capillary malformation-arteriovenous malformation 2		HP:0025104	PMID:28730721	PCS		1/1			P	HPO:probinson[2022-11-26]
OMIM:618196	Capillary malformation-arteriovenous malformation 2		HP:0003829	OMIM:618196	IEA					I	HPO:skoehler[2019-04-18]
OMIM:618196	Capillary malformation-arteriovenous malformation 2		HP:0003593	PMID:28730721	PCS		1/1			C	HPO:probinson[2022-11-26]
OMIM:618196	Capillary malformation-arteriovenous malformation 2		HP:0001009	OMIM:618196	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618196	Capillary malformation-arteriovenous malformation 2		HP:0000006	PMID:28730721	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:618196	Capillary malformation-arteriovenous malformation 2		HP:0030713	OMIM:618196	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002322	PMID:35198730	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0032506	PMID:35198730	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002015	PMID:35198730	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002059	PMID:35198730	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002067	PMID:39810750;PMID:35198730	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0001300	PMID:39810750	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0003596	PMID:39810750;PMID:35198730	PCS		3/4			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0001288	PMID:39810750;PMID:35198730	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002186	PMID:35198730	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002451	PMID:35198730	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0003584	PMID:35198730	PCS		1/3			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002063	PMID:39810750;PMID:35198730	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0000020	PMID:35198730	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002075	PMID:35198730	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002174	PMID:35198730	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0002172	PMID:35198730	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0030904	PMID:35198730	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0007010	PMID:39810750	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0001423	PMID:35198730	PCS					I	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0001268	PMID:39810750;PMID:35198730	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0000751	PMID:35198730	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0000511	PMID:35198730	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0001336	PMID:35198730	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:301142	Neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairement		HP:0001347	PMID:35198730	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:600901	Fanconi anemia, complementation group E		HP:0003213	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0003214	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000365	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000486	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0004322	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000086	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000085	OMIM:600901	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000081	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001909	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000815	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001903	OMIM:600901	TAS					P	HPO:skoehler[2013-06-13]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000957	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000953	OMIM:600901	TAS					P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001627	OMIM:600901	TAS					P	HPO:skoehler[2015-12-30]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000978	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0009943	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001249	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000252	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0003221	OMIM:600901	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001263	OMIM:600901	TAS		20/20			P	HPO:skoehler[2017-07-13];HPO:skoehler[2019-04-18]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001518	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000007	PMID:11001585	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-06]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000568	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0009777	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001896	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0009778	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001873	OMIM:600901	TAS					P	HPO:skoehler[2013-06-13]
OMIM:600901	Fanconi anemia, complementation group E		HP:0003974	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000028	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001876	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001017	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0001875	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:600901	Fanconi anemia, complementation group E		HP:0000104	OMIM:600901	IEA					P	HPO:iea[2009-02-17]
OMIM:177050	Protrusio acetabuli		HP:0003179	PMID:629604	PCS					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-04]
OMIM:177050	Protrusio acetabuli		HP:0003273	PMID:629604	PCS					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-04]
OMIM:177050	Protrusio acetabuli		HP:0030838	OMIM:177050;PMID:629604	PCS		20/20			P	HPO:lccarmody[2018-10-04];HPO:skoehler[2018-10-08]
OMIM:177050	Protrusio acetabuli		HP:0000006	OMIM:177050	IEA					I	HPO:iea[2009-02-17]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0002465	PMID:25480035	PCS		4/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-12-10];HPO:probinson[2020-12-12]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0000750	PMID:25480035	PCS		4/5			P	HPO:probinson[2020-12-10];HPO:probinson[2020-12-10];HPO:probinson[2020-12-12]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0002384	PMID:25480035	PCS	HP:0003621	2/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-12-10];HPO:probinson[2020-12-12]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0001263	PMID:25480035	PCS		5/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-12-10];HPO:probinson[2020-12-12]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0003593	PMID:25480035	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-12]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0001290	PMID:25480035	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-10];HPO:probinson[2020-12-12]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0000007	PMID:25480035	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-10]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0001249	PMID:25480035	PCS		5/5			P	HPO:skoehler[2015-08-05];HPO:probinson[2020-12-10];HPO:probinson[2020-12-12]
OMIM:616193	Intellectual developmental disorder, autosomal recessive 47		HP:0001634	PMID:25480035	PCS		1/5			P	HPO:probinson[2020-12-10];HPO:probinson[2020-12-12]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0001320	PMID:31168944	PCS		5/6			P	HPO:probinson[2020-06-29];HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0007979	PMID:31168944	PCS					P	HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0000486	PMID:31168944	PCS		1/3			P	HPO:probinson[2020-06-29];HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0004322	PMID:31168944	PCS					P	HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0030147	PMID:31168944	PCS		1/6			P	HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0002066	PMID:31168944	PCS					P	HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0001260	PMID:31168944	PCS		5/5			P	HPO:probinson[2020-06-29];HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0001270	PMID:31168944	PCS		5/5			P	HPO:probinson[2020-06-29];HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0007010	PMID:31168944	PCS					P	HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0007772	PMID:31168944	PCS					P	HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0000007	PMID:31168944	PCS					I	HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0007256	PMID:31168944	PCS		4/5			P	HPO:probinson[2020-06-29];HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0000648	PMID:31168944	PCS		1/3			P	HPO:probinson[2020-06-29];HPO:probinson[2020-06-29]
OMIM:618800	Spinocerebellar ataxia, autosomal recessive 28		HP:0000545	PMID:31168944	PCS					P	HPO:probinson[2020-06-29]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0000110	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0000891	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0001177	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0001762	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0002023	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0000089	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0004392	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0000007	OMIM:601389	IEA					I	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0000912	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0001539	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0002944	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0000796	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0001973	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:601389	Cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction		HP:0008635	OMIM:601389	IEA					P	HPO:iea[2009-02-17]
OMIM:613955	Amyloidosis, primary localized cutaneous, 2		HP:0012309	OMIM:613955	TAS					P	HPO:probinson[2013-08-10]
OMIM:613955	Amyloidosis, primary localized cutaneous, 2		HP:0000989	OMIM:613955	TAS					P	HPO:probinson[2013-08-10]
OMIM:613955	Amyloidosis, primary localized cutaneous, 2		HP:0000006	OMIM:613955	TAS					I	HPO:probinson[2013-01-09]
OMIM:620353	Spermatogenic failure 82		HP:0032560	PMID:35228300	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620353	Spermatogenic failure 82		HP:0034011	PMID:35228300	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620353	Spermatogenic failure 82		HP:0003251	PMID:35228300	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620353	Spermatogenic failure 82		HP:0011462	PMID:35228300	PCS		2/2			C	HPO:probinson[2023-06-18]
OMIM:620353	Spermatogenic failure 82		HP:0000007	PMID:35228300	PCS					I	HPO:probinson[2023-06-18]
OMIM:620353	Spermatogenic failure 82		HP:0032558	PMID:35228300	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620353	Spermatogenic failure 82		HP:0032559	PMID:35228300	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:616839	Exercise intolerance, riboflavin-responsive		HP:0003200	PMID:26933868	PCS					P	HPO:probinson[2017-06-23]
OMIM:616839	Exercise intolerance, riboflavin-responsive		HP:0000007	PMID:26933868	PCS					I	HPO:probinson[2017-06-23]
OMIM:616839	Exercise intolerance, riboflavin-responsive		HP:0003546	PMID:26933868	PCS					P	HPO:probinson[2017-06-23]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0004325	PMID:15689435	PCS		1/1			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000286	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0003676	PMID:17172942	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0010804	OMIM:300260	TAS					P	HPO:skoehler[2014-11-26]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002540	PMID:16080119;PMID:17172942	PCS		8/19			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001773	PMID:24478188	PCS		3/4			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001250	PMID:16080119;PMID:17172942;PMID:24478188;PMID:20035514	PCS		14/30			P	HPO:probinson[2021-05-10];HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000160	OMIM:300260	IEA					P	HPO:iea[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001252	PMID:15689435	PCS		1/1			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002063	OMIM:300260	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001251	OMIM:300260	IEA					P	HPO:iea[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002020	OMIM:300260	IEA					P	HPO:iea[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002061	PMID:16080119;PMID:20035514	PCS		17/18			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000716	OMIM:300260	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0031473	OMIM:300260	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0025336	PMID:15689435;PMID:24478188	PCS		6/6			P	HPO:probinson[2021-05-10];HPO:probinson[2021-05-10];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0003763	PMID:15689435;PMID:20035514	PCS		7/10			P	HPO:probinson[2021-05-10];HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000297	PMID:16080119	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000252	PMID:17172942	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001344	PMID:15689435;PMID:16080119;PMID:17172942;PMID:24478188	PCS		22/25			P	HPO:probinson[2021-05-10];HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0011968	PMID:15689435	PCS		1/1			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001263	PMID:17172942	PCS		7/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002072	PMID:20035514	PCS		8/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0011800	PMID:17172942	PCS		5/7			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002191	OMIM:300260	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0032169	PMID:24478188	PCS		5/5			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001419	OMIM:300260	IEA					I	HPO:iea[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000729	PMID:15689435;PMID:17172942;PMID:20035514	PCS		13/17			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0008762	PMID:20035514	PCS		9/9			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0004209	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002307	PMID:16080119;PMID:20035514	PCS		18/19			P	HPO:probinson[2021-05-10];HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000400	PMID:17172942	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000047	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000248	PMID:24478188	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000369	OMIM:300260	IEA					P	HPO:iea[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000687	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0008947	PMID:17172942	PCS		7/7			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000582	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000463	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002121	PMID:15689435	PCS		1/1			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0010864	PMID:16080119;PMID:24478188;PMID:20035514	PCS		26/26			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002719	PMID:17172942;PMID:24478188	PCS		9/12			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0007021	PMID:20035514	PCS		3/9			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000817	OMIM:300260;PMID:20035514	PCS		19/19			P	HPO:probinson[2021-05-10];HPO:skoehler[2010-06-18]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0005709	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000739	PMID:20035514	PCS		6/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0012450	PMID:24478188;PMID:20035514	PCS		9/14			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000733	PMID:15689435;PMID:17172942;PMID:20035514	PCS		11/17			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000218	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000256	PMID:17172942	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0032989	PMID:15689435	PCS		1/1			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0008936	PMID:20035514	PCS		8/9			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002015	OMIM:300260	IEA					P	HPO:iea[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000431	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002133	PMID:24478188	PCS		5/5			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0031936	PMID:15689435;PMID:16080119;PMID:24478188	PCS		18/18			P	HPO:probinson[2021-05-10];HPO:probinson[2021-05-10];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002376	PMID:15689435;PMID:20035514	PCS		4/10			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000272	PMID:24478188	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0011344	PMID:15689435	TAS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0005280	OMIM:300260	IEA					P	HPO:iea[2009-02-17]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0032792	PMID:15689435	PCS		1/1			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000508	PMID:17172942	PCS		2/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000426	PMID:17172942	PCS		1/7			P	HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0002205	PMID:16080119;PMID:20035514	PCS		12/18			P	HPO:probinson[2021-05-10];HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0001510	PMID:17172942	PCS		0/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:300260	Intellectual developmental disorder, X-linked syndromic, Lubs type		HP:0000028	PMID:15689435;PMID:17172942;PMID:20035514	PCS		5/17			P	HPO:probinson[2021-05-10];HPO:iea[2009-02-17];HPO:probinson[2021-05-10]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0002069	PMID:25401298	PCS		15/15			P	HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0003676	PMID:25401298	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0003621	PMID:25401298	PCS		14/15			C	HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0001272	PMID:25401298	PCS		HP:0040283			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0011463	PMID:25401298	PCS		1/15			C	HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0011198	PMID:25401298	PCS		16/16			P	HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0001251	PMID:25401298	PCS		1/16			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0032794	PMID:25401298	PCS		14/15			P	HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0001268	PMID:25401298	PCS		9/15			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0001337	PMID:25401298	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0000006	PMID:25401298	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-28]
OMIM:616187	Epilepsy, progressive myoclonic 7		HP:0001336	PMID:25401298	PCS		16/16			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-01-28]
OMIM:264080	Progesterone resistance		HP:0001939	OMIM:264080	IEA					P	HPO:iea[2009-02-17]
OMIM:264080	Progesterone resistance		HP:0008222	OMIM:264080	IEA					P	HPO:iea[2009-02-17]
OMIM:264080	Progesterone resistance		HP:0000007	OMIM:264080	IEA					I	HPO:iea[2009-02-17]
OMIM:606394	Maturity-onset diabetes of the young 6		HP:0004904	PMID:10545951	PCS	HP:0011462				P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:606394	Maturity-onset diabetes of the young 6		HP:0000006	PMID:10545951	PCS					I	HPO:probinson[2013-03-24];HPO:probinson[2020-07-20]
OMIM:175860	Porokeratosis punctata palmaris et plantaris		HP:0200044	OMIM:175860	IEA					P	HPO:skoehler[2015-01-27]
OMIM:175860	Porokeratosis punctata palmaris et plantaris		HP:0000006	OMIM:175860	IEA					I	HPO:iea[2009-02-17]
OMIM:175860	Porokeratosis punctata palmaris et plantaris		HP:0007613	OMIM:175860	IEA					P	HPO:iea[2009-02-17]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0001682	OMIM:217085	TAS					P	HPO:skoehler[2010-06-20]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0003577	PMID:25427950	PCS		1/1			C	HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0001674	OMIM:217085	IEA					P	HPO:iea[2009-02-17]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0001233	OMIM:217085	TAS					P	HPO:probinson[2009-02-17]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0005696	PMID:25427950	PCS		1/1			P	HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0001162	OMIM:217085	IEA					P	HPO:iea[2009-02-17]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0011968	PMID:25427950	PCS		1/1			P	HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0001263	PMID:25427950	PCS		0/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2024-03-08]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0001680	PMID:25427950	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0004691	PMID:25427950	PCS		1/1			P	HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0011802	PMID:25427950	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0010055	PMID:25427950	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0000316	PMID:25427950	PCS		0/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2024-03-08]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0000007	PMID:25427950	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2022-10-06]
OMIM:217085	Congenital heart defects, hamartomas of tongue, and polysyndactyly		HP:0000202	PMID:25427950	PCS		0/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2024-03-08]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0003577	PMID:11841538	PCS		2/2			C	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0002224	PMID:9738775;PMID:11841538	PCS		13/14			P	HPO:probinson[2023-07-13];HPO:skoehler[2015-08-23];HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0001596	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0001030	PMID:11841538	PCS		2/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0045075	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0100792	PMID:11841538	PCS		2/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0001508	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0001626	PMID:11841538	PCS		0/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0000972	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0000653	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0004756	PMID:9738775	PCS		1/12			P	HPO:skoehler[2015-10-05];HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0001644	PMID:9738775	PCS		9/12			P	HPO:skoehler[2015-08-23];HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0009804	OMIM:605676	IEA					P	HPO:skoehler[2015-08-23]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0031319	OMIM:605676	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0025493	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0011421	PMID:9738775	PCS		2/12			C	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0000969	OMIM:605676	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0008066	PMID:11841538	PCS	HP:0003577	2/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0100759	PMID:9738775	PCS					P	HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0100613	PMID:9738775	PCS		3/12			C	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0000007	PMID:9738775	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0001635	PMID:9738775	PCS					P	HPO:skoehler[2015-10-05];HPO:probinson[2020-07-17]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0025524	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0008404	PMID:11841538	PCS		1/2			P	HPO:probinson[2023-07-13]
OMIM:605676	Cardiomyopathy, dilated, with woolly hair and keratoderma		HP:0000982	PMID:9738775	PCS		12/12			P	HPO:skoehler[2015-08-23];HPO:probinson[2020-07-17]
OMIM:615465	Hartsfield syndrome		HP:0000286	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0006988	PMID:23812909	PCS		2/7			P	HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0002069	PMID:23812909	PCS		1/7			P	HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0000161	PMID:23812909	PCS		1/7			P	HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0001274	PMID:23812909	PCS		5/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0008213	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0000316	PMID:23812909	PCS		2/7			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0006870	PMID:23812909;OMIM:615465	PCS		13/17			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0000873	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0003228	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0000358	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0000175	PMID:23812909	PCS		4/7			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0001363	OMIM:615465	TAS		HP:0040283			P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0000252	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0000054	PMID:23812909	PCS		3/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0005466	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0001263	PMID:23812909;OMIM:615465	PCS		16/16		HP:0012828	P	HPO:skoehler[2019-02-22];HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0100257	PMID:23812909	PCS		6/7			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0000601	PMID:23812909	PCS		2/7			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0002507	PMID:23812909	PCS		2/7			P	HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0001319	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0001159	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0000047	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0001510	PMID:23812909	PCS		6/6			P	HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0000006	PMID:23812909	PCS					I	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0000204	PMID:23812909	PCS		3/7			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0000028	PMID:23812909	PCS		3/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-03-23]
OMIM:615465	Hartsfield syndrome		HP:0000369	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:615465	Hartsfield syndrome		HP:0000445	OMIM:615465	TAS					P	HPO:skoehler[2013-10-22]
OMIM:601410	Diabetes mellitus, transient neonatal, 1		HP:0008255	OMIM:601410	IEA					P	HPO:iea[2009-02-17]
OMIM:601410	Diabetes mellitus, transient neonatal, 1		HP:0001944	OMIM:601410	IEA					P	HPO:iea[2009-02-17]
OMIM:601410	Diabetes mellitus, transient neonatal, 1		HP:0001525	OMIM:601410	IEA					P	HPO:iea[2009-02-17]
OMIM:601410	Diabetes mellitus, transient neonatal, 1		HP:0003074	OMIM:601410	IEA					P	HPO:iea[2009-02-17]
OMIM:601410	Diabetes mellitus, transient neonatal, 1		HP:0001511	OMIM:601410	IEA					P	HPO:iea[2009-02-17]
OMIM:601410	Diabetes mellitus, transient neonatal, 1		HP:0000006	OMIM:601410	IEA					I	HPO:skoehler[2019-04-18]
OMIM:611603	Lissencephaly 3		HP:0002069	PMID:17584854	PCS		2/5			P	HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0003577	PMID:17584854	PCS					C	HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0002365	PMID:17584854	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0001250	PMID:17584854	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0001274	PMID:17584854	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0001252	OMIM:611603	TAS					P	HPO:skoehler[2014-11-26]
OMIM:611603	Lissencephaly 3		HP:0001251	OMIM:611603	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611603	Lissencephaly 3		HP:0001290	OMIM:611603	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611603	Lissencephaly 3		HP:0031882	PMID:17584854	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0002282	OMIM:611603	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611603	Lissencephaly 3		HP:0001270	OMIM:611603	IEA					P	HPO:iea[2009-02-17]
OMIM:611603	Lissencephaly 3		HP:0002119	PMID:17584854	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0001302	PMID:17584854	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0003623	PMID:17584854	PCS					C	HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0001320	PMID:17584854	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0000252	PMID:17584854	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0002510	PMID:17584854	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0002079	PMID:17584854	PCS		2/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0001263	PMID:17584854	PCS		5/5			P	HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0010818	PMID:17584854	PCS		1/5			P	HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0032389	PMID:17584854	PCS		1/8			P	HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0001339	OMIM:611603	IEA					P	HPO:iea[2009-02-17]
OMIM:611603	Lissencephaly 3		HP:0000006	PMID:17584854	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:611603	Lissencephaly 3		HP:0002126	OMIM:611603	TAS					P	HPO:skoehler[2012-10-17]
OMIM:617272	Glaucoma 3, primary congenital, E		HP:0000485	PMID:27270174	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617272	Glaucoma 3, primary congenital, E		HP:0012040	PMID:27270174	PCS					P	HPO:probinson[2022-12-18]
OMIM:617272	Glaucoma 3, primary congenital, E		HP:0007906	PMID:27270174	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:617272	Glaucoma 3, primary congenital, E		HP:0012796	PMID:27270174	PCS					P	HPO:probinson[2022-12-18]
OMIM:617272	Glaucoma 3, primary congenital, E		HP:0000006	PMID:27270174	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617272	Glaucoma 3, primary congenital, E		HP:0000501	PMID:27270174	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0002069	PMID:29630738	PCS		5/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0002521	PMID:29630738	PCS		1/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0006813	PMID:29630738	PCS		1/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0002353	PMID:29630738	PCS		9/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0001288	PMID:29630738	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0002123	PMID:29630738	PCS		6/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0002376	PMID:29630738	PCS		2/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0001332	PMID:29630738	PCS		1/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0001272	PMID:29630738	PCS		1/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0002121	PMID:29630738	PCS		5/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0010819	PMID:29630738	PCS		1/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0001263	PMID:29630738	PCS		9/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0003593	PMID:29630738	PCS		6/9			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0100660	PMID:29630738	PCS		1/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0100023	PMID:29630738	PCS		3/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0011463	PMID:29630738	PCS		3/9			C	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0000817	PMID:29630738	PCS		1/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0032792	PMID:29630738	PCS		3/9			P	HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0200134	PMID:29630738	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0002305	PMID:29630738	PCS		1/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0000006	PMID:29630738	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-18]
OMIM:618141	Epileptic encephalopathy, early infantile, 67		HP:0001249	PMID:29630738	PCS		8/8			P	HPO:probinson[2022-12-18]
OMIM:617514	Immunodeficiency 52		HP:0006528	PMID:27242165	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0020072	PMID:27242165	PCS		1/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0003593	PMID:27242165;PMID:27522155	PCS		5/8			C	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0001508	PMID:27522155	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0002719	PMID:27242165;PMID:27522155	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-30];HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0002958	PMID:27522155	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0002716	PMID:27242165	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0001888	PMID:27242165	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0006532	PMID:27242165	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0001522	PMID:27242165	PCS		1/3			C	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0001744	PMID:27242165	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0003623	PMID:27522155	PCS		3/5			C	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0005403	PMID:27522155	PCS		5/5			P	HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0004313	PMID:27242165	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0002110	PMID:27242165	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0032247	PMID:27242165	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0031379	PMID:27522155	PCS		5/5			P	HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0010975	PMID:27522155	PCS		0/5			P	HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0003819	PMID:27242165	PCS		1/3			C	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0500270	PMID:27242165	PCS		3/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0040089	PMID:27522155	PCS		0/5			P	HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0000007	PMID:27242165	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0001973	PMID:27242165	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0004844	PMID:27242165	PCS		2/3			P	HPO:probinson[2021-05-30]
OMIM:617514	Immunodeficiency 52		HP:0002720	PMID:27522155	PCS		3/3			P	HPO:probinson[2024-03-15]
OMIM:617514	Immunodeficiency 52		HP:0002721	PMID:27242165	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-30]
OMIM:182230	Septooptic dysplasia		HP:0001331	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0010627	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0004322	OMIM:182230	TAS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:182230	Septooptic dysplasia		HP:0001274	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0001263	OMIM:182230	PCS		20/20			P	HPO:skoehler[2019-02-22];HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0010442	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0000609	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0009381	OMIM:182230	TAS					P	HPO:skoehler[2012-10-17]
OMIM:182230	Septooptic dysplasia		HP:0000007	OMIM:182230	TAS					I	HPO:skoehler[2012-10-17]
OMIM:182230	Septooptic dysplasia		HP:0000824	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0000873	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0007766	OMIM:182230	PCS					P	HPO:probinson[2012-04-04]
OMIM:182230	Septooptic dysplasia		HP:0000006	OMIM:182230	TAS					I	HPO:skoehler[2012-10-17]
OMIM:619539	Neuroocular syndrome		HP:0001212	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0004322	PMID:33314030	PCS		2/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000482	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0100694	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0006191	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000639	PMID:33314030	PCS		2/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000518	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0002816	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0010296	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000635	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000637	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0009743	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0009900	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000278	PMID:29556724	PCS		1/3		HP:0012825	P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001763	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001249	PMID:29556724	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0002553	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000176	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000494	PMID:29556724	PCS		2/6			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000252	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001187	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0002870	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000574	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000490	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001263	PMID:29556724;PMID:33314030	PCS		6/8			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0031354	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0011800	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001182	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0012775	PMID:29556724	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0030822	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0011094	PMID:29556724	PCS		1/3		HP:0012825	P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000729	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000646	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000767	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001537	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0007750	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000568	PMID:33314030	PCS		3/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000527	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0004209	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000960	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000006	PMID:29556724	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000369	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000687	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001655	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001792	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0003577	PMID:29556724	PCS		3/3			C	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000540	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0003691	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001270	PMID:29556724	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0100786	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0100789	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000739	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000612	PMID:29556724;PMID:33314030	PCS		3/8			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000579	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0006970	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000659	PMID:33314030	PCS		3/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0002714	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000378	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001348	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000336	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000577	PMID:29556724	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0008936	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0001088	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0007968	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000750	PMID:29556724	PCS		3/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0002299	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0009908	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0030001	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0010812	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000508	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0100719	PMID:29556724	PCS		1/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000664	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0007018	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000545	PMID:29556724	PCS		2/3			P	HPO:probinson[2021-10-23]
OMIM:619539	Neuroocular syndrome		HP:0000501	PMID:33314030	PCS		1/5			P	HPO:probinson[2021-10-23]
OMIM:238700	Hyperlysinemia, type I		HP:0003532	PMID:23890588	PCS		2/2			P	HPO:probinson[2024-02-09];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0003297	PMID:23890588;PMID:10775527	PCS		3/3			P	HPO:probinson[2024-02-09];HPO:probinson[2024-02-09];HPO:probinson[2023-03-16]
OMIM:238700	Hyperlysinemia, type I		HP:0001250	PMID:23890588	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:238700	Hyperlysinemia, type I		HP:0001252	OMIM:238700	IEA					P	HPO:iea[2009-02-17]
OMIM:238700	Hyperlysinemia, type I		HP:0003131	PMID:23890588	PCS		1/2			P	HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0003593	PMID:23890588	PCS		2/2			C	HPO:skoehler[2014-04-13];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0002161	PMID:23890588;PMID:10775527	PCS		3/3			P	HPO:probinson[2024-02-09];HPO:iea[2009-02-17];HPO:probinson[2023-03-16]
OMIM:238700	Hyperlysinemia, type I		HP:0100543	OMIM:238700	TAS					P	HPO:skoehler[2014-04-13]
OMIM:238700	Hyperlysinemia, type I		HP:0500163	PMID:23890588	PCS		2/2			P	HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0001903	OMIM:238700	IEA					P	HPO:iea[2009-02-17]
OMIM:238700	Hyperlysinemia, type I		HP:0034464	PMID:23890588	PCS		2/2			P	HPO:probinson[2024-02-09];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0000736	PMID:23890588	PCS		1/2			P	HPO:skoehler[2014-04-13]
OMIM:238700	Hyperlysinemia, type I		HP:0500204	PMID:23890588	PCS		1/1			P	HPO:probinson[2024-02-09];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0000752	PMID:23890588	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0003268	PMID:23890588	PCS		2/2			P	HPO:probinson[2024-02-09];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0002312	PMID:23890588	PCS		1/2			P	HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0000750	PMID:23890588	PCS		1/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0002373	PMID:23890588	PCS		1/2			P	HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0002075	PMID:23890588	PCS		1/2			P	HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0500208	PMID:23890588	PCS		1/1			P	HPO:probinson[2024-02-09];HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0001083	OMIM:238700	IEA					P	HPO:iea[2009-02-17]
OMIM:238700	Hyperlysinemia, type I		HP:0000609	PMID:23890588	PCS		1/2			P	HPO:probinson[2024-02-09]
OMIM:238700	Hyperlysinemia, type I		HP:0000007	PMID:10775527	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-16]
OMIM:238700	Hyperlysinemia, type I		HP:6000270	OMIM:238700	TAS					P	HPO:probinson[2024-02-09]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0011870	PMID:19828703	PCS		1/1			P	HPO:probinson[2024-03-14]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0003593	PMID:19828703	PCS		1/1			C	HPO:probinson[2024-03-14]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0031364	PMID:19828703	PCS		1/1			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-22];HPO:probinson[2024-03-14]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0000978	PMID:19828703	PCS		1/1			P	HPO:skoehler[2012-10-17];HP:probinson[2019-01-22];HPO:probinson[2024-03-14]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0011894	PMID:7929844	PCS		4/4			P	HP:probinson[2019-01-22];HP:probinson[2019-01-22]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0000421	PMID:19828703	PCS		1/1			P	HPO:skoehler[2012-10-17];HP:probinson[2019-01-22];HPO:probinson[2024-03-14]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0011873	PMID:19828703	PCS		0/1			P	HPO:skoehler[2014-11-27];HP:probinson[2019-01-22];HPO:probinson[2024-03-14]
OMIM:614009	Bleeding disorder, platelet-type, 13, susceptibility to		HP:0000006	PMID:7929844	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-01-22]
OMIM:131950	Epidermolysis bullosa simplex, Ogna type		HP:0007585	OMIM:131950	IEA					P	HPO:iea[2009-02-17]
OMIM:131950	Epidermolysis bullosa simplex, Ogna type		HP:0000978	OMIM:131950	IEA					P	HPO:iea[2009-02-17]
OMIM:131950	Epidermolysis bullosa simplex, Ogna type		HP:0008401	OMIM:131950	IEA					P	HPO:iea[2009-02-17]
OMIM:131950	Epidermolysis bullosa simplex, Ogna type		HP:0000006	OMIM:131950	IEA					I	HPO:iea[2009-02-17]
OMIM:131950	Epidermolysis bullosa simplex, Ogna type		HP:0020117	PMID:11851880	PCS					P	HPO:probinson[2019-09-07]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0002542	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0003676	OMIM:146500	IEA					C	HPO:skoehler[2010-06-19]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000640	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0001278	OMIM:146500	IEA					P	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0002067	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0002063	OMIM:146500	IEA					P	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000020	OMIM:146500	TAS					P	HPO:probinson[2012-06-10]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0001251	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0002180	OMIM:146500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0012332	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0100543	OMIM:146500	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0003745	OMIM:146500	IEA					I	HPO:skoehler[2010-06-19]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0001347	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0001089	OMIM:146500	IEA					P	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0003202	OMIM:146500	IEA					P	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000970	OMIM:146500	IEA					P	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0001300	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000012	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0003487	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0001260	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0003581	OMIM:146500	IEA					C	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0002172	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000508	OMIM:146500	IEA					P	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000007	OMIM:146500	TAS					I	HPO:skoehler[2013-08-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000802	OMIM:146500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000966	OMIM:146500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0000006	OMIM:146500	IEA					I	HPO:iea[2009-02-17]
OMIM:146500	Multiple system atrophy 1, susceptibility to		HP:0001337	OMIM:146500	IEA					P	HPO:iea[2009-02-17]
OMIM:194320	Woronets trait		HP:0005540	OMIM:194320	IEA					P	HPO:iea[2009-02-17]
OMIM:194320	Woronets trait		HP:0000006	OMIM:194320	IEA					I	HPO:iea[2009-02-17]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0025584	PMID:29887215	PCS		3/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000473	PMID:29887215	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0005864	PMID:29887215	PCS		1/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0003577	PMID:29887215	PCS		5/5			C	HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0002650	PMID:29887215	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0012366	PMID:29887215	PCS		2/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000508	PMID:29887215	PCS	HP:0003577	4/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000921	PMID:29887215	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000767	OMIM:618155	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000007	PMID:29887215	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000768	PMID:29887215	PCS		1/5			P	HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000773	PMID:29887215	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000577	PMID:29887215	PCS		4/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:618155	Ophthalmoplegia, external, with rib and vertebral anomalies		HP:0000544	PMID:29887215	PCS	HP:0003577	5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-05-19]
OMIM:613000	Palmoplantar keratoderma, nonepidermolytic, focal 1		HP:0003621	PMID:8595410	PCS					C	HPO:probinson[2023-02-11]
OMIM:613000	Palmoplantar keratoderma, nonepidermolytic, focal 1		HP:0033707	PMID:8595410	PCS					P	HPO:probinson[2023-02-11]
OMIM:613000	Palmoplantar keratoderma, nonepidermolytic, focal 1		HP:0032152	OMIM:613000	TAS					P	HPO:skoehler[2019-09-07]
OMIM:613000	Palmoplantar keratoderma, nonepidermolytic, focal 1		HP:0007475	PMID:8595410	PCS		0/13			P	HPO:probinson[2023-02-11]
OMIM:613000	Palmoplantar keratoderma, nonepidermolytic, focal 1		HP:0000982	PMID:8595410	PCS		13/13			P	HPO:probinson[2013-04-07];HPO:probinson[2023-02-11]
OMIM:613000	Palmoplantar keratoderma, nonepidermolytic, focal 1		HP:0007502	PMID:8595410	PCS		13/13			P	HPO:probinson[2023-02-11]
OMIM:613000	Palmoplantar keratoderma, nonepidermolytic, focal 1		HP:0000006	PMID:8595410	PCS					I	HPO:probinson[2013-04-07];HPO:probinson[2023-02-11]
OMIM:142000	Hemoglobin-Delta locus		HP:0001903	OMIM:142000	TAS					P	HPO:iea[2015-02-15]
OMIM:142000	Hemoglobin-Delta locus		HP:0005560	OMIM:142000	TAS					P	HPO:iea[2015-02-15]
OMIM:142000	Hemoglobin-Delta locus		HP:0000006	OMIM:142000	IEA					I	HPO:iea[2009-02-17]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001298	PMID:31969900;PMID:32779419	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002421	PMID:27182039;PMID:32559514;PMID:30804983;PMID:32779419	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000365	PMID:27182039;PMID:28940506;PMID:27743463;PMID:25868664;PMID:23993194;PMID:32779419	PCS		7/52			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000486	PMID:27182039;PMID:28940506;PMID:30804983;PMID:34602956;PMID:25868664;PMID:23993194	PCS		11/52			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001332	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0030059	PMID:27290639;PMID:28940506;PMID:25868664;PMID:23993194	PCS		18/20			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0004322	PMID:28940506;PMID:27743463;PMID:25868664;PMID:23993194	PCS		27/53			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002384	PMID:27182039;PMID:28940506;PMID:27743463;PMID:25868664	PCS		2/38			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002020	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003593	PMID:28940506;PMID:32559514;PMID:30804983;PMID:27743463;PMID:25868664;PMID:23993194	PCS		17/77			C	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0012745	PMID:27290639;PMID:27182039;PMID:28940506;PMID:34602956;PMID:26404457;PMID:27099744;PMID:25868664;PMID:23993194	PCS		8/68			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0010602	PMID:23993193	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0033725	PMID:28940506;PMID:34602956;PMID:27099744;PMID:25868664;PMID:23993194;PMID:32779419	PCS		13/50			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0012469	PMID:28940506;PMID:27743463;PMID:31969900	PCS		1/37			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000518	PMID:23993193	PCS		2/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000639	PMID:27182039;PMID:28940506;PMID:30804983;PMID:34602956;PMID:27743463;PMID:25868664;PMID:31969900;PMID:32779419;PMID:23993194	PCS		12/59			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000238	PMID:34602956	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002415	PMID:27743463	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003348	PMID:27182039;PMID:34602956;PMID:26404457;PMID:31969900;PMID:32779419	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003623	PMID:27290639;PMID:28940506;PMID:27182039;PMID:27743463;PMID:26404457;PMID:25868664;PMID:27099744;PMID:31969900;PMID:23993194;PMID:32779419	PCS		57/84			C	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000494	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000252	PMID:28940506;PMID:23993193;PMID:27743463;PMID:30804983;PMID:31969900;PMID:27099744;PMID:25868664;PMID:23993194	PCS		30/63			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-26];ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003487	PMID:27182039	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011924	PMID:27290639;PMID:28940506;PMID:23993193;PMID:25868664;PMID:23993194	PCS		15/36			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011925	PMID:27290639;PMID:28940506;PMID:25868664	PCS		8/19			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002151	PMID:27290639;PMID:28940506;PMID:27182039;PMID:32559514;PMID:23993193;PMID:32779419;PMID:23993194;PMID:30804983;PMID:30771478;PMID:34602956;PMID:27743463;PMID:31442532;PMID:27099744;PMID:25868664;PMID:31969900	PCS		99/99			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011923	PMID:27290639;PMID:28940506;PMID:23993193;PMID:25868664;PMID:23993194	PCS		16/36			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000007	PMID:23993193	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000527	PMID:27290639;PMID:28940506;PMID:30804983;PMID:27099744;PMID:25868664;PMID:23993194	PCS		9/66			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000648	PMID:28940506;PMID:25868664;PMID:32779419;PMID:23993194	PCS		8/52			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000369	PMID:27290639;PMID:28940506;PMID:25868664;PMID:31969900;PMID:27099744;PMID:23993194;PMID:32779419	PCS		15/68			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000126	PMID:31442532	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002487	PMID:27182039	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000343	PMID:27290639;PMID:28940506;PMID:27182039;PMID:30804983;PMID:25868664;PMID:27099744;PMID:23993194;PMID:32779419	PCS		12/68			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001272	PMID:28940506;PMID:25868664;PMID:27099744;PMID:32779419;PMID:23993194	PCS		9/49			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002240	PMID:27182039;PMID:32779419	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001947	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011120	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0040155	PMID:32559514	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0007663	PMID:28940506;PMID:25868664;PMID:23993194	PCS		7/51			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002119	PMID:27182039;PMID:28940506;PMID:23993193;PMID:34602956;PMID:30804983;PMID:30771478;PMID:27099744;PMID:25868664;PMID:23993194;PMID:32779419	PCS		18/59			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002910	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003688	PMID:26404457	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001942	PMID:27182039;PMID:26404457;PMID:31969900;PMID:32779419	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000336	PMID:30804983	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001667	PMID:27743463	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0004313	PMID:26404457	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002015	PMID:30804983;PMID:31969900;PMID:32779419	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003621	PMID:27290639;PMID:28940506	PCS		2/38			C	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002650	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001321	PMID:31442532	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000232	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002013	PMID:27182039;PMID:32559514;PMID:34602956;PMID:31969900;PMID:32779419	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0005487	PMID:27182039;PMID:34602956	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0025190	PMID:28940506;PMID:30771478;PMID:23993194	PCS		8/37			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002092	PMID:28940506;PMID:27743463;PMID:26404457;PMID:25868664;PMID:27099744;PMID:23993194	PCS		5/63			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011344	OMIM:615471	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000508	PMID:27290639;PMID:27182039;PMID:28940506;PMID:25868664;PMID:27099744;PMID:23993194	PCS		5/66			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001712	PMID:27743463	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0008347	PMID:27290639;PMID:28940506;PMID:23993193;PMID:25868664;PMID:23993194	PCS		18/36			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002007	PMID:30804983;PMID:32779419	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000347	PMID:27290639;PMID:28940506;PMID:25868664;PMID:27099744;PMID:23993194;PMID:32779419	PCS		4/66			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002126	PMID:31442532	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000286	PMID:27290639;PMID:27182039;PMID:28940506;PMID:34602956;PMID:27099744;PMID:25868664;PMID:23993194	PCS		11/67			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002188	PMID:23993193	PCS		1/6			P	HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001773	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001250	PMID:28940506;PMID:27743463;PMID:25868664;PMID:27099744;PMID:23993194	PCS		9/17			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0012707	PMID:28940506;PMID:27182039;PMID:34602956;PMID:26404457;PMID:32779419	PCS		20/26			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001252	PMID:27182039;PMID:32559514;PMID:28940506;PMID:23993193;PMID:32779419;PMID:23993194;PMID:34602956;PMID:27743463;PMID:30771478;PMID:30804983;PMID:26404457;PMID:31969900;PMID:25868664;PMID:27099744	PCS		84/90			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-26];ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001251	PMID:27290639;PMID:28940506;PMID:25868664;PMID:23993194	PCS		7/47			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011463	PMID:28940506;PMID:27743463;PMID:25868664	PCS		9/64			C	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000319	PMID:27290639;PMID:28940506;PMID:27182039;PMID:30804983;PMID:34602956;PMID:26404457;PMID:27099744;PMID:25868664;PMID:23993194;PMID:32779419	PCS		10/70			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011220	PMID:27290639;PMID:27182039;PMID:28940506;PMID:34602956;PMID:27099744;PMID:25868664;PMID:23993194	PCS		14/67			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000316	PMID:27290639;PMID:28940506;PMID:32559514;PMID:27099744;PMID:25868664;PMID:23993194	PCS		8/66			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001888	PMID:26404457	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003429	PMID:27182039;PMID:26404457	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001643	PMID:28940506;PMID:27743463	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0004755	PMID:28940506;PMID:27743463	PCS		3/46			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0007109	PMID:28940506;PMID:25868664;PMID:27099744;PMID:23993194	PCS		6/48			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003202	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000574	PMID:27290639;PMID:28940506;PMID:27182039;PMID:30804983;PMID:34602956;PMID:25868664;PMID:27099744;PMID:23993194	PCS		11/68			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001266	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002079	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000331	PMID:27182039;PMID:34602956	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011968	PMID:28940506;PMID:32559514;PMID:27182039;PMID:30804983;PMID:34602956;PMID:26404457;PMID:25868664;PMID:23993194;PMID:32779419	PCS		36/51			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001263	PMID:32559514;PMID:27182039;PMID:28940506;PMID:23993193;PMID:27743463;PMID:30771478;PMID:31442532;PMID:31969900;PMID:32779419	PCS		58/59		HP:0012828	P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-26];ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001537	PMID:27182039	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000047	PMID:27182039;PMID:28940506;PMID:31969900;PMID:27099744;PMID:25868664;PMID:23993194	PCS		8/44			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001655	PMID:28940506;PMID:27743463	PCS		7/46			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000023	PMID:34602956	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0030674	PMID:30771478;PMID:27743463;PMID:34602956	PCS		3/11			C	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002283	PMID:27290639;PMID:27182039;PMID:30804983;PMID:27099744;PMID:25868664;PMID:23993194	PCS		39/39			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011675	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002280	PMID:28940506;PMID:27099744;PMID:25868664;PMID:31969900;PMID:23993194	PCS		13/49			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001508	PMID:28940506;PMID:30804983;PMID:27743463;PMID:26404457;PMID:25868664;PMID:23993194	PCS		32/55			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002719	PMID:28940506	PCS		10/37			P	HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001903	PMID:30804983;PMID:32779419	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001987	PMID:28940506;PMID:32559514;PMID:23993193;PMID:30771478;PMID:30804983;PMID:27743463;PMID:27099744;PMID:25868664;PMID:31969900;PMID:23993194;PMID:32779419	PCS		26/58			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0008314	PMID:27290639;PMID:28940506;PMID:25868664;PMID:23993194	PCS		12/35			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003648	PMID:27182039;PMID:32559514;PMID:34602956;PMID:30771478;PMID:26404457	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000411	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001347	PMID:27182039	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003128	PMID:23993193	PCS		7/7			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-26]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001622	PMID:27290639;PMID:28940506;PMID:27099744;PMID:25868664;PMID:23993194	PCS		7/52			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000275	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0002059	PMID:27182039;PMID:28940506;PMID:23993193;PMID:27743463;PMID:34602956;PMID:25868664;PMID:27099744;PMID:32779419;PMID:23993194	PCS		32/62			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-26];ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000431	PMID:27290639;PMID:28940506;PMID:27182039;PMID:32559514;PMID:34602956;PMID:25868664;PMID:27099744;PMID:23993194	PCS		15/68			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0011427	PMID:31969900	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0034648	PMID:32779419	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001639	PMID:28940506;PMID:34602956;PMID:31442532;PMID:27099744;PMID:25868664;PMID:23993194	PCS		15/56			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001518	PMID:27290639;PMID:28940506;PMID:27099744;PMID:25868664;PMID:23993194	PCS		28/44			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001636	PMID:28940506;PMID:27743463	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001357	OMIM:615471	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000664	PMID:27290639;PMID:25868664;PMID:27099744;PMID:23993194	PCS		4/28			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001631	PMID:28940506;PMID:27743463;PMID:25868664;PMID:27099744;PMID:23993194	PCS		4/19			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001510	OMIM:615471	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0000028	PMID:28940506;PMID:27182039;PMID:34602956;PMID:31442532;PMID:25868664;PMID:27099744;PMID:31969900;PMID:23993194	PCS		11/46			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0003535	PMID:31442532	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-27]
OMIM:615471	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)		HP:0001875	PMID:28940506;PMID:26404457;PMID:25868664;PMID:27099744;PMID:23993194;PMID:32779419	PCS		13/70			P	ORCID:0000-0002-0736-9199[2024-11-27];HPO:skoehler[2013-11-18];HPO:probinson[2024-11-27]
OMIM:619263	Nephrotic syndrome, type 24		HP:0003621	PMID:33232676	PCS		2/4			C	HPO:probinson[2021-05-31]
OMIM:619263	Nephrotic syndrome, type 24		HP:0033132	PMID:33232676	PCS					P	HPO:probinson[2021-05-31]
OMIM:619263	Nephrotic syndrome, type 24		HP:0011463	PMID:33232676	PCS		2/4			C	HPO:probinson[2021-05-31]
OMIM:619263	Nephrotic syndrome, type 24		HP:0000097	PMID:33232676	PCS		4/4			P	HPO:probinson[2021-05-31]
OMIM:619263	Nephrotic syndrome, type 24		HP:0000007	PMID:33232676	PCS					I	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:619263	Nephrotic syndrome, type 24		HP:0031266	PMID:33232676	PCS		4/4			P	HPO:probinson[2021-05-31]
OMIM:619263	Nephrotic syndrome, type 24		HP:0012588	PMID:33232676	PCS		4/4			P	HPO:probinson[2021-05-31]
OMIM:613028	Glioma susceptibility 2		HP:0033681	PMID:12085208	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:613028	Glioma susceptibility 2		HP:0002858	PMID:12085208	PCS		1/1			P	HPO:probinson[2023-07-11]
OMIM:613028	Glioma susceptibility 2		HP:0025710	PMID:12085208	PCS		1/1			C	HPO:probinson[2023-07-11]
OMIM:613028	Glioma susceptibility 2		HP:0000006	PMID:12085208	PCS					I	HPO:probinson[2023-07-11]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0004420	OMIM:612336	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0000979	OMIM:612336	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0100724	OMIM:612336	IEA					P	HPO:skoehler[2015-01-21]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0002638	OMIM:612336	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0001038	OMIM:612336	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0000006	PMID:7545463	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-03-18]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0004855	OMIM:612336	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0005305	OMIM:612336	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612336	Thrombophilia, hereditary, due to protein S deficiency, autosomal		HP:0002204	OMIM:612336	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604232	Leber congenital amaurosis-3 (LCA3)/Retinitis pigmentosa, juvenile, autosomal recessive		HP:0000572	PMID:21310915	PCS		10/10			P	HPO:probinson[2013-02-19]
OMIM:604232	Leber congenital amaurosis-3 (LCA3)/Retinitis pigmentosa, juvenile, autosomal recessive		HP:0001133	PMID:21310915	PCS					P	HPO:probinson[2013-02-19]
OMIM:604232	Leber congenital amaurosis-3 (LCA3)/Retinitis pigmentosa, juvenile, autosomal recessive		HP:0000662	PMID:21310915	PCS		2/8			P	HPO:probinson[2013-02-19]
OMIM:604232	Leber congenital amaurosis-3 (LCA3)/Retinitis pigmentosa, juvenile, autosomal recessive		HP:0000639	PMID:21310915	PCS		10/10			P	HPO:probinson[2013-02-19]
OMIM:604232	Leber congenital amaurosis-3 (LCA3)/Retinitis pigmentosa, juvenile, autosomal recessive		HP:0003593	PMID:21310915	PCS		1/10			C	HPO:probinson[2022-08-04]
OMIM:604232	Leber congenital amaurosis-3 (LCA3)/Retinitis pigmentosa, juvenile, autosomal recessive		HP:0000007	PMID:21310915	PCS					I	HPO:probinson[2013-01-09]
OMIM:604232	Leber congenital amaurosis-3 (LCA3)/Retinitis pigmentosa, juvenile, autosomal recessive		HP:0003623	PMID:21310915	PCS		9/10			C	HPO:probinson[2022-08-04]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0003621	PMID:30790670	PCS		1/1			C	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0001663	PMID:27861123	PCS		4/6		HP:0025377	P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30];HP:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0001695	PMID:27861123	PCS		3/3			P	HP:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0004751	PMID:30790670	PCS		1/1			P	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0005184	PMID:30790670	PCS		0/1			P	HPO:probinson[2021-10-30];HPO:probinson[2024-03-14]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0031677	PMID:30790670	PCS		1/1			P	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0034040	PMID:30790670	PCS		1/1			P	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0011463	PMID:27861123	PCS		1/3			C	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0011462	PMID:27861123	PCS		2/3			C	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0006682	PMID:30790670	PCS		1/1			P	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0001657	PMID:27861123	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0000007	PMID:27861123	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0001962	PMID:30790670	PCS		1/1			P	HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0001279	PMID:30790670;PMID:27861123	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-30];HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0004756	PMID:27861123	PCS		3/3		HP:0025377	P	HPO:skoehler[2015-01-19];HPO:probinson[2021-10-30]
OMIM:614021	Ventricular tachycardia, catecholaminergic polymorphic, 3		HP:0001699	OMIM:614021	TAS					P	HPO:skoehler[2012-10-17]
OMIM:620384	Auditory neuropathy, autosomal dominant 2		HP:0003621	PMID:36300302	PCS					C	HPO:probinson[2023-11-11]
OMIM:620384	Auditory neuropathy, autosomal dominant 2		HP:0003676	PMID:36300302	PCS					C	HPO:probinson[2023-11-11]
OMIM:620384	Auditory neuropathy, autosomal dominant 2		HP:0000407	PMID:36300302	PCS					P	HPO:probinson[2023-11-11]
OMIM:620384	Auditory neuropathy, autosomal dominant 2		HP:0000006	PMID:36300302	PCS					I	HPO:probinson[2023-07-15]
OMIM:620384	Auditory neuropathy, autosomal dominant 2		HP:0001963	PMID:36300302	PCS					P	HPO:probinson[2023-11-11]
OMIM:610247	Esophagitis, eosinophilic, 1		HP:0100633	OMIM:610247	IEA					P	HPO:skoehler[2015-01-27]
OMIM:610247	Esophagitis, eosinophilic, 1		HP:0002015	OMIM:610247	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610247	Esophagitis, eosinophilic, 1		HP:0001880	OMIM:610247	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610247	Esophagitis, eosinophilic, 1		HP:0002013	OMIM:610247	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610247	Esophagitis, eosinophilic, 1		HP:0001508	OMIM:610247	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610247	Esophagitis, eosinophilic, 1		HP:0410019	OMIM:610247	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616636	Immunodeficiency 44		HP:0001298	OMIM:616636	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616636	Immunodeficiency 44		HP:0002850	PMID:26122121	PCS		1/2			P	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0410242	PMID:26122121	PCS		0/2			P	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0020088	PMID:23391734	PCS		1/5			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0002151	PMID:26122121	PCS		1/2			P	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0003593	PMID:23391734	PCS		1/3			C	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0031964	PMID:26122121	PCS		1/2			P	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0040204	PMID:26122121	PCS		2/2			P	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0031691	PMID:23391734	PCS		3/5			P	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0011463	PMID:23391734	PCS		2/5			C	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0000007	PMID:23391734	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0001888	PMID:26122121	PCS		2/2			P	HPO:probinson[2022-07-02]
OMIM:616636	Immunodeficiency 44		HP:0002720	PMID:26122121	PCS		2/2			P	HPO:probinson[2022-07-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002069	PMID:39013458	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000365	PMID:39013458;PMID:19264732	PCS		38/119			P	ORCID:0000-0002-0736-9199[2024-08-02];HPO:sdoelken[2009-02-17]
OMIM:610253	Kleefstra syndrome 1		HP:0000486	PMID:39013458	PCS		24/76			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0004322	PMID:39013458	PCS		10/111			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001250	PMID:39013458	PCS		18/18			P	HPO:sdoelken[2009-02-17];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0010808	PMID:20945554	PCS		HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001252	PMID:39013458	PCS	HP:0011463	49/125			P	HPO:sdoelken[2009-02-17]
OMIM:610253	Kleefstra syndrome 1		HP:0002020	PMID:39013458	PCS		29/114			P	HPO:sdoelken[2010-12-03]
OMIM:610253	Kleefstra syndrome 1		HP:0010806	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000280	PMID:20945554	PCS	HP:0003621	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000716	PMID:39013458	PCS		9/104			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000718	PMID:39013458	PCS		27/104			P	HPO:sdoelken[2009-02-17];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000717	PMID:39013458	PCS		55/104			P	HPO:sdoelken[2010-12-03]
OMIM:610253	Kleefstra syndrome 1		HP:0000316	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000954	OMIM:610253	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610253	Kleefstra syndrome 1		HP:0000158	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001643	PMID:39013458	PCS		2/110			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0003745	PMID:20945554	PCS					I	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001763	PMID:39013458	PCS		30/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001249	PMID:39013458	PCS		112/125			P	HPO:sdoelken[2009-02-17]
OMIM:610253	Kleefstra syndrome 1		HP:0000252	PMID:39013458;PMID:19264732	PCS		33/124			P	ORCID:0000-0002-0736-9199[2024-08-02];HPO:sdoelken[2009-02-17]
OMIM:610253	Kleefstra syndrome 1		HP:0000054	PMID:20945554	PCS		HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000010	PMID:39013458	PCS		6/115			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000098	PMID:39013458	PCS		8/111			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001344	PMID:39013458	PCS		10/53			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000695	PMID:20945554	PCS	HP:0003577	HP:0040283			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0011968	PMID:39013458	PCS		31/38			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002197	PMID:39013458	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001382	PMID:39013458	PCS		30/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001263	PMID:39013458	PCS		114/124			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0011800	PMID:20945554	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0033454	PMID:39013458	PCS		9/104			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0011641	PMID:39013458	PCS		1/117			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000767	PMID:39013458	PCS		8/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001537	PMID:39013458	PCS		2/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000722	PMID:39013458	PCS		9/104			P	HPO:skoehler[2012-10-17]
OMIM:610253	Kleefstra syndrome 1		HP:0004209	PMID:39013458	PCS		3/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0007359	PMID:39013458	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000047	PMID:39013458	PCS		1/115			P	HPO:sdoelken[2010-12-03]
OMIM:610253	Kleefstra syndrome 1		HP:0000006	PMID:39013458	PCS					I	HPO:sdoelken[2009-02-17];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000248	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002786	PMID:20945554	PCS		HP:0040284			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000126	PMID:39013458	PCS		2/115			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001655	PMID:39013458	PCS		5/109			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000582	PMID:20945554	PCS		HP:0040282			P	HPO:sdoelken[2009-02-17];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000463	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001156	PMID:20945554	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000540	PMID:39013458	PCS		41/41			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000023	PMID:39013458	PCS		4/115			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002121	PMID:39013458	PCS		4/117			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0012368	PMID:20945554	PCS					P	HPO:skoehler[2013-10-22];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002719	PMID:39013458	PCS		52/56			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001629	PMID:39013458	PCS		10/109			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000739	PMID:39013458	PCS		26/104			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0012450	PMID:39013458	PCS		59/119			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0006695	PMID:39013458	PCS		1/109			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001822	PMID:39013458	PCS		4/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000733	PMID:20945554;PMID:39013458	PCS		18/114			P	ORCID:0000-0002-0736-9199[2024-08-02];HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0007302	PMID:39013458	PCS		3/104			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0006335	PMID:20945554	PCS	HP:0003621	HP:0040283			P	HPO:sdoelken[2012-07-31];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000750	PMID:20945554	PCS		HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001520	PMID:39013458	PCS		19/91			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002650	PMID:39013458	PCS		0/84			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001762	PMID:39013458	PCS		5/125			P	HPO:sdoelken[2010-12-03]
OMIM:610253	Kleefstra syndrome 1		HP:0002376	PMID:39013458	PCS		35/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000232	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002373	PMID:39013458	PCS		6/118			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0010819	PMID:39013458	PCS		2/117			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000272	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000074	PMID:39013458	PCS		2/115			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000709	PMID:39013458	PCS		14/104			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002808	PMID:39013458	PCS		5/125			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001518	PMID:39013458	PCS		12/92			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000107	PMID:39013458	PCS		2/115			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0007334	PMID:39013458	PCS		1/117			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0025502	PMID:39013458	PCS		39/109			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000741	PMID:20945554	PCS	HP:0003621	HP:0040284			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0002205	PMID:20945554	PCS		HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000664	PMID:20945554	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001631	PMID:39013458	PCS		16/23			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0007018	PMID:39013458	PCS		7/104			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000028	PMID:39013458	PCS		2/115			P	HPO:sdoelken[2010-12-03]
OMIM:610253	Kleefstra syndrome 1		HP:0000303	PMID:20945554	PCS		HP:0040282			P	HPO:sdoelken[2009-02-17];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001513	PMID:19264732	PCS	HP:0011463	HP:0040282			P	HPO:sdoelken[2009-02-17]
OMIM:610253	Kleefstra syndrome 1		HP:0001513	PMID:39013458	PCS		13/109			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0001710	PMID:20945554	PCS					P	HPO:sdoelken[2010-12-03];HPO:probinson[2024-08-02]
OMIM:610253	Kleefstra syndrome 1		HP:0000742	PMID:39013458	PCS		10/104			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:616622	Immunodeficiency 42		HP:0009098	PMID:17564971	PCS		5/7			P	HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0011370	PMID:17564971	PCS		3/7			P	HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0011463	PMID:17564971	PCS		1/7			C	HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0003593	PMID:17564971	PCS		6/7			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0020087	PMID:17564971	PCS		6/7			P	HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0002240	PMID:17564971	PCS		2/7			P	HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0000778	PMID:17564971	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0000007	PMID:17564971	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0011107	PMID:17564971	PCS		1/7			P	HPO:probinson[2023-02-17]
OMIM:616622	Immunodeficiency 42		HP:0001744	PMID:17564971	PCS		2/7			P	HPO:probinson[2023-02-17]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0000365	PMID:21353196	PCS		0/4			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0004586	OMIM:613982	TAS					P	HPO:probinson[2013-08-10]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0003179	OMIM:613982	TAS					P	HPO:probinson[2013-08-10]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0001382	PMID:21353196	PCS		0/4			P	HPO:probinson[2013-08-10]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0003155	PMID:21353196	PCS		4/4			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0000592	PMID:21353196	PCS		4/4			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0003593	PMID:21353196	PCS		3/3			C	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0001270	PMID:21353196	PCS		4/4			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0033154	PMID:21353196	PCS		2/2			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0002979	PMID:21353196	PCS		4/4			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0000007	PMID:21353196	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0002812	OMIM:613982	TAS					P	HPO:probinson[2013-08-10]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0000703	PMID:21353196	PCS		0/4			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0002757	PMID:21353196	PCS		4/4			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0002659	PMID:21353196	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0006488	PMID:21353196	PCS		4/4			P	HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0002953	PMID:21353196	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-14]
OMIM:613982	Osteogenesis imperfecta, type VI		HP:0004568	OMIM:613982	TAS					P	HPO:probinson[2013-08-10]
OMIM:270750	Spastic paraplegia 23		HP:0001045	PMID:14681889	PCS		4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0000275	OMIM:270750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270750	Spastic paraplegia 23		HP:0000252	PMID:14681889	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0001003	PMID:14681889	PCS		4/4			P	HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0002650	PMID:14681889	PCS		1/4			P	HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0003487	PMID:14681889	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0005586	PMID:14681889	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0004771	PMID:14681889	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0003691	PMID:14681889	PCS		1/4			P	HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0007340	PMID:14681889	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0011463	PMID:14681889	PCS		4/4			C	HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0009830	PMID:14681889	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0000007	PMID:14681889	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0002505	PMID:14681889	PCS		3/4			P	HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0001258	PMID:14681889	PCS	HP:0011463	4/4		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0000278	PMID:14681889	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0000347	PMID:14681889	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:270750	Spastic paraplegia 23		HP:0001347	PMID:14681889	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0002257	PMID:18950741	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0001696	PMID:18950741;PMID:23261302	PCS		7/12			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24];HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0002110	PMID:18950741;PMID:23261302	PCS		11/12			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24];HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0003251	PMID:18950741	PCS			MALE		P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0033036	PMID:23261302	IEA		6/6			P	HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0012735	PMID:18950741	PCS					P	HPO:probinson[2020-07-24]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0002090	PMID:18950741	PCS	HP:0003623				P	HPO:probinson[2020-07-24]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0011109	PMID:23261302	PCS		6/6			P	HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0011108	PMID:18950741	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0012265	PMID:18950741	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-24]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0012256	PMID:23261302	PCS		5/5			P	HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0000007	PMID:18950741	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0000403	PMID:18950741	PCS		6/6			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24];HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0000389	PMID:23261302	PCS		6/6			P	HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0002643	PMID:23261302	PCS		3/5			P	HPO:probinson[2022-02-28]
OMIM:612444	Ciliary dyskinesia, primary, 9, with or without situs inversus		HP:0003623	PMID:18950741	PCS		4/4			C	HPO:probinson[2022-02-28]
OMIM:187360	Temporal arteritis		HP:0003565	OMIM:187360	IEA					P	HPO:iea[2009-02-17]
OMIM:187360	Temporal arteritis		HP:0008030	OMIM:187360	IEA					P	HPO:iea[2009-02-17]
OMIM:187360	Temporal arteritis		HP:0000618	OMIM:187360	IEA					P	HPO:iea[2009-02-17]
OMIM:187360	Temporal arteritis		HP:0000006	OMIM:187360	IEA					I	HPO:iea[2009-02-17]
OMIM:614035	Deafness, autosomal recessive 29		HP:0000365	PMID:11163249	PCS					P	HPO:probinson[2013-08-10]
OMIM:614035	Deafness, autosomal recessive 29		HP:0000407	OMIM:614035	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614035	Deafness, autosomal recessive 29		HP:0003680	OMIM:614035	TAS					C	HPO:skoehler[2015-12-30]
OMIM:614035	Deafness, autosomal recessive 29		HP:0000007	PMID:11163249	PCS					I	HPO:probinson[2013-08-10]
OMIM:614753	Malan syndrome		HP:0000483	PMID:20673863	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000486	PMID:20673863;PMID:22301465	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000540	PMID:20673863;PMID:22301465	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000160	PMID:20673863;PMID:22301465	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0001252	PMID:20673863;PMID:22301465	PCS		4/5			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0003196	PMID:22301465	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0001270	PMID:20673863;PMID:22301465	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000639	PMID:20673863;PMID:22301465	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0011463	PMID:22301465	PCS		1/2			C	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000739	PMID:20673863	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0001548	PMID:20673863	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0100807	PMID:20673863	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0002119	PMID:20673863	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000256	PMID:20673863	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000212	PMID:22301465	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000278	PMID:22301465	PCS		0/2			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0001249	PMID:20673863;PMID:22301465	PCS		5/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0003623	PMID:22301465	PCS		1/2			C	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000275	PMID:20673863;PMID:22301465	PCS		4/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000494	PMID:20673863;PMID:22301465	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000750	PMID:20673863;PMID:22301465	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0002650	PMID:20673863;PMID:22301465	PCS		3/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0002673	PMID:20673863;PMID:22301465	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000232	PMID:20673863;PMID:22301465	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000276	PMID:20673863;PMID:22301465	PCS		4/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0002079	PMID:20673863	PCS		1/3			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0011800	PMID:22301465	PCS		1/2			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000729	PMID:20673863;PMID:22301465	PCS		3/5			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000965	PMID:20673863	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000767	PMID:20673863;PMID:22301465	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0430029	PMID:22301465	PCS		0/1			P	HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0006288	PMID:20673863	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000348	PMID:20673863;PMID:22301465	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0005616	PMID:20673863;PMID:22301465	PCS		4/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000006	PMID:20673863	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-03-04]
OMIM:614753	Malan syndrome		HP:0000303	PMID:20673863;PMID:22301465	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0002664	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000939	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000716	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0008231	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000938	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000739	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000712	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000978	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000713	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0003745	OMIM:219080	IEA					I	HPO:skoehler[2010-06-19]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000311	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0001268	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0003202	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0001442	OMIM:219080	TAS					I	HPO:skoehler[2019-04-18]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0001065	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0003581	OMIM:219080	IEA					C	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000709	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0002808	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0008221	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000822	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0001956	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0003118	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0002920	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0000963	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:219080	ACTH-independent macronodular adrenal hyperplasia		HP:0001579	OMIM:219080	IEA					P	HPO:iea[2009-02-17]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0008905	OMIM:601438	IEA					P	HPO:iea[2009-02-17]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0005687	OMIM:601438	IEA					P	HPO:iea[2009-02-17]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0001156	OMIM:601438	IEA					P	HPO:iea[2009-02-17]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0000926	OMIM:601438	IEA					P	HPO:iea[2009-02-17]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0005792	OMIM:601438	IEA					P	HPO:iea[2009-02-17]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0010049	OMIM:601438	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0000007	OMIM:601438	TAS					I	HPO:skoehler[2017-07-13]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0002812	OMIM:601438	IEA					P	HPO:iea[2009-02-17]
OMIM:601438	Rhizomelic dysplasia, Patterson-Lowry type		HP:0010743	OMIM:601438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610535	Glaucoma 1, open angle, M		HP:0001133	OMIM:610535	TAS					P	HPO:probinson[2012-09-16]
OMIM:610535	Glaucoma 1, open angle, M		HP:0012108	OMIM:610535	TAS					P	HPO:probinson[2009-02-17]
OMIM:610535	Glaucoma 1, open angle, M		HP:0000006	OMIM:610535	TAS					I	HPO:skoehler[2009-02-17]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000286	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0030732	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001773	OMIM:157800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000486	PMID:27426734	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0004322	PMID:27426734	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001252	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0002020	PMID:29467388;PMID:27426734	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000085	PMID:27426734	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0012304	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0011387	PMID:27426734	PCS		1/5			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0011461	PMID:29467388	PCS		1/1			C	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000316	PMID:27426734	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0009702	PMID:29467388;PMID:27426734	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0008734	PMID:27426734	PCS		2/2	MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000358	PMID:29467388;PMID:27426734	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0002578	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0002750	PMID:27426734	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0011968	PMID:27426734	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000293	PMID:27426734	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001382	PMID:29467388;PMID:27426734	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0002949	PMID:27426734	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0008441	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000403	PMID:27426734	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000405	OMIM:157800	TAS					P	HPO:probinson[2009-02-17]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0008368	PMID:29467388;PMID:27426734	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001653	OMIM:157800	TAS					P	HPO:probinson[2009-02-17]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000006	PMID:27426734	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0008527	PMID:27426734	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000369	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001655	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000582	PMID:27426734	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0003577	PMID:27426734	PCS		6/6			C	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000343	PMID:29467388;PMID:27426734	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000463	PMID:29467388;PMID:27426734	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001156	PMID:27426734	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0005278	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0005473	PMID:27426734	PCS		1/5			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001508	PMID:29467388;PMID:27426734	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001629	PMID:27426734	PCS		1/6			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000414	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000977	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000776	PMID:27426734	PCS		1/6			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000154	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000076	PMID:27426734	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0002650	PMID:27426734	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000431	PMID:29467388	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000592	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0010579	PMID:27426734	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0011623	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0010584	OMIM:157800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000902	OMIM:157800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000506	PMID:27426734	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000629	PMID:27426734	PCS		6/6			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0000508	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001558	PMID:29467388	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:157800	Cardiospondylocarpofacial syndrome		HP:0001631	PMID:27426734	PCS		1/6			P	HPO:probinson[2022-04-24]
OMIM:120450	Comedones, familial dyskeratotic		HP:0000006	OMIM:120450	IEA					I	HPO:iea[2009-02-17]
OMIM:120450	Comedones, familial dyskeratotic		HP:0000951	OMIM:120450	IEA					P	HPO:iea[2009-02-17]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0001892	OMIM:207731	IEA					P	HPO:skoehler[2010-06-20]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0002593	OMIM:207731	IEA					P	HPO:iea[2009-02-17]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0003075	OMIM:207731	IEA					P	HPO:iea[2009-02-17]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0007430	OMIM:207731	IEA					P	HPO:iea[2009-02-17]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0004471	OMIM:207731	IEA					P	HPO:iea[2009-02-17]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0000007	OMIM:207731	IEA					I	HPO:iea[2009-02-17]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0001888	OMIM:207731	IEA					P	HPO:iea[2009-02-17]
OMIM:207731	Aplasia cutis congenita with intestinal lymphangiectasia		HP:0000245	OMIM:207731	IEA					P	HPO:skoehler[2009-02-17]
OMIM:601809	Spondylospinal thoracic dysostosis		HP:0002089	OMIM:601809	IEA					P	HPO:iea[2009-02-17]
OMIM:601809	Spondylospinal thoracic dysostosis		HP:0001040	OMIM:601809	IEA					P	HPO:iea[2009-02-17]
OMIM:601809	Spondylospinal thoracic dysostosis		HP:0000327	OMIM:601809	IEA					P	HPO:iea[2009-02-17]
OMIM:601809	Spondylospinal thoracic dysostosis		HP:0002804	OMIM:601809	IEA					P	HPO:iea[2009-02-17]
OMIM:601809	Spondylospinal thoracic dysostosis		HP:0000007	OMIM:601809	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:601809	Spondylospinal thoracic dysostosis		HP:0010306	OMIM:601809	IEA					P	HPO:skoehler[2010-06-18]
OMIM:601809	Spondylospinal thoracic dysostosis		HP:0000347	OMIM:601809	IEA					P	HPO:iea[2009-02-17]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0003587	OMIM:610910	IEA					C	HPO:skoehler[2010-06-19]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0025044	PMID:17287477	PCS		1/12			P	HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0006517	PMID:17287477	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0030049	PMID:17287477	PCS		1/12			P	HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0020050	PMID:17287477	PCS		12/12			P	HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0002094	PMID:17287477	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0012735	PMID:14695413	PCS					P	HPO:skoehler[2014-03-24];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0012418	PMID:12501225	PCS		1/1			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0002090	PMID:17287477	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0031996	PMID:14695413	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-06-14];HPO:probinson[2022-12-03]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0002091	PMID:12501225	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0045051	PMID:14695413	PCS					P	HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0001217	PMID:14695413	PCS		HP:0040284			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0100749	PMID:14695413	PCS		HP:0040284			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0000961	PMID:14695413	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-06-14];HPO:probinson[2022-12-03]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0003745	OMIM:610910	IEA					I	HPO:skoehler[2010-06-19]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0002205	PMID:17287477	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-06-14]
OMIM:610910	Pulmonary alveolar proteinosis, acquired		HP:0002105	OMIM:610910	IEA					P	HPO:skoehler[2010-06-19]
OMIM:618394	Immunodeficiency 60		HP:0005425	PMID:28530713	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0002113	PMID:28530713	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0002850	PMID:28530713	PCS		2/3			P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0005479	PMID:28530713	PCS		2/3			P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0100280	PMID:28530713	PCS	HP:0011462	1/3			P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0002583	PMID:28530713	PCS	HP:0003593				P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0002110	PMID:28530713	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0031808	PMID:28530713	PCS		3/3			P	HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0030374	PMID:28530713	PCS		3/3			P	HPO:probinson[2020-09-27];HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0032229	PMID:28530713	PCS		1/3			P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0100279	PMID:28530713	PCS	HP:0003621	1/3			P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0001945	PMID:28530713	PCS					P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0002206	PMID:28530713	PCS					P	HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0001744	PMID:28530713	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0000006	PMID:28530713	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-27]
OMIM:618394	Immunodeficiency 60		HP:0001876	PMID:28530713	PCS					P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0002720	PMID:28530713	PCS		3/3			P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0002028	PMID:28530713	PCS		3/3			P	HPO:probinson[2020-09-28]
OMIM:618394	Immunodeficiency 60		HP:0004315	PMID:28530713	PCS		2/3			P	HPO:probinson[2020-09-28]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000286	PMID:33150406	PCS		3/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0001397	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0002465	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000483	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000387	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000486	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000540	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0001252	PMID:33150406	PCS		2/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000020	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0002020	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0004283	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0008070	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0009183	PMID:33150406	PCS		5/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000639	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0002719	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0010055	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0100704	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000414	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000218	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0001643	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0002019	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000278	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0001249	PMID:33150406	PCS		9/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000358	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000154	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000252	PMID:33150406;PMID:29276005	PCS		7/8			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0011968	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000293	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000490	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0001263	PMID:33150406	PCS		8/8			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0003186	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0004691	PMID:33150406	PCS		3/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0011344	PMID:29276005	PCS		1/1			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0034197	PMID:29276005	PCS		1/1			C	HPO:probinson[2022-08-20];HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000629	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000508	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0002007	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0001511	PMID:33150406;PMID:29276005	PCS		4/10			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0007018	PMID:33150406	PCS		1/9			P	HPO:probinson[2022-08-20]
OMIM:619934	Intellectual developmental disorder, autosomal dominant 68		HP:0000006	PMID:29276005	PCS					I	HPO:probinson[2022-08-20]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0002367	PMID:24598713	PCS		6/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0003577	PMID:24598713	PCS		2/6			C	HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0003621	PMID:24598713	PCS		2/6			C	HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0002133	PMID:24598713	PCS		2/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0002384	PMID:24598713	PCS		6/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0003593	PMID:24598713	PCS		1/6			C	HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0033258	PMID:24598713	PCS		2/6			P	HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0031258	PMID:24598713	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0025709	PMID:24598713	PCS		1/6			C	HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0000718	PMID:24598713	PCS		3/6			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0000007	PMID:24598713	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0002119	PMID:24598713	PCS		3/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0007334	PMID:24598713	PCS		6/6			P	HPO:probinson[2023-02-09]
OMIM:612691	Polymicrogyria, bilateral temporooccipital		HP:0002126	PMID:24598713	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-09]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0001320	OMIM:602482	TAS					P	HPO:skoehler[2013-05-03]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0009918	PMID:10713890	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000691	PMID:10713890	PCS		4/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000272	PMID:10713890	PCS		4/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0011800	OMIM:602482	TAS					P	HPO:skoehler[2015-11-15]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000627	PMID:10713890	PCS		9/9			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000407	OMIM:602482	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0011484	PMID:10713890	PCS		2/6			P	HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0011120	OMIM:602482	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000316	PMID:10713890	PCS		5/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000668	OMIM:602482	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0007676	PMID:10713890	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0001643	OMIM:602482	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0001631	OMIM:602482	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000520	OMIM:602482	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000006	PMID:10713890	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-02]
OMIM:602482	Axenfeld-Rieger syndrome, type 3		HP:0000501	PMID:10713890	PCS		1/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-02]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0002069	PMID:31318984;PMID:34788397	PCS		3/4			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0025682	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0002188	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0002066	PMID:34788397	PCS		3/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001252	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0003593	PMID:34788397	PCS		1/3			C	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0032794	PMID:34788397	PCS		2/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001508	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0011463	PMID:34788397	PCS		2/3			C	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0000752	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001347	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0008936	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001265	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0006813	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0000750	PMID:34788397	PCS		3/3			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0011968	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0010819	PMID:34788397	PCS		2/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001263	PMID:34788397	PCS		2/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0002094	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0011147	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0011344	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0034197	PMID:31318984	PCS		1/1			C	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0000729	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0011451	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0032792	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001712	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001511	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001257	PMID:31318984	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0000006	PMID:31318984	PCS					I	HPO:probinson[2023-03-25]
OMIM:620145	Developmental and epileptic encephalopathy 109		HP:0001336	PMID:34788397	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:116860	Cerebral cavernous malformations 1		HP:0001250	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0003011	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0003829	OMIM:116860	IEA					I	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0002170	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0006576	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0007797	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0033522	PMID:10545614	PCS					P	HPO:probinson[2022-01-23]
OMIM:116860	Cerebral cavernous malformations 1		HP:0002315	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0002514	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:116860	Cerebral cavernous malformations 1		HP:0000006	PMID:10545614	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-01-23]
OMIM:116860	Cerebral cavernous malformations 1		HP:0000951	OMIM:116860	IEA					P	HPO:iea[2009-02-17]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0009073	PMID:7783167	PCS					P	HPO:iea[2009-02-17]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0000662	PMID:7783167	PCS		4/4	FEMALE		P	HP:probinson[2018-07-07]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0001518	OMIM:300076	IEA			MALE		P	HPO:iea[2009-02-17]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0001319	PMID:7783167	PCS			MALE	HP:0012828	P	HP:probinson[2018-07-07]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0000009	OMIM:300076	IEA					P	HPO:iea[2009-02-17]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0001258	OMIM:300076	IEA			FEMALE		P	HPO:skoehler[2010-06-20]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0001423	PMID:7783167	PCS					I	HPO:iea[2009-02-17]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0003811	PMID:7783167	PCS			MALE		C	HPO:probinson[2013-12-15]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0008348	PMID:7783167	PCS					P	HPO:probinson[2013-12-15]
OMIM:300076	Immunoneurologic disorder, X-linked		HP:0001348	PMID:7783167	PCS					P	HPO:iea[2009-02-17]
OMIM:614592	Bent bone dysplasia syndrome		HP:0003577	PMID:22387015	PCS		4/4			C	HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000695	PMID:22387015	PCS		1/3			P	HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0001156	OMIM:614592	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614592	Bent bone dysplasia syndrome		HP:0001591	OMIM:614592	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614592	Bent bone dysplasia syndrome		HP:0004440	PMID:22387015	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0005474	PMID:22387015	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000272	OMIM:614592	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614592	Bent bone dysplasia syndrome		HP:0011800	OMIM:614592	TAS					P	HPO:skoehler[2013-11-28]
OMIM:614592	Bent bone dysplasia syndrome		HP:0003173	PMID:22387015	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0001090	PMID:22387015	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0034530	PMID:22387015	PCS		4/4			P	HPO:probinson[2023-03-31]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000316	PMID:22387015	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0008665	PMID:22387015	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000212	OMIM:614592	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614592	Bent bone dysplasia syndrome		HP:0001433	OMIM:614592	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000894	PMID:22387015;OMIM:614592	PCS		14/14			P	HPO:probinson[2023-02-10];HPO:skoehler[2012-10-17]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000006	PMID:22387015	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0001007	PMID:22387015	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000369	OMIM:614592	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614592	Bent bone dysplasia syndrome		HP:0000347	OMIM:614592	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300062	Intellectual developmental disorder, X-linked 14		HP:0002465	OMIM:300062	IEA					P	HPO:iea[2009-02-17]
OMIM:300062	Intellectual developmental disorder, X-linked 14		HP:0001250	OMIM:300062	IEA					P	HPO:iea[2009-02-17]
OMIM:300062	Intellectual developmental disorder, X-linked 14		HP:0000053	OMIM:300062	IEA					P	HPO:iea[2009-02-17]
OMIM:300062	Intellectual developmental disorder, X-linked 14		HP:0001999	OMIM:300062	IEA					P	HPO:iea[2009-02-17]
OMIM:300062	Intellectual developmental disorder, X-linked 14		HP:0001417	OMIM:300062	IEA					I	HPO:iea[2009-02-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0008936	PMID:35240055	PCS		1/4			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0002444	PMID:35240055	PCS		1/3			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0000750	PMID:35240055	PCS		5/5			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0001250	PMID:35240055	PCS		5/5			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0001263	PMID:35240055	PCS		5/5			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0003593	PMID:35240055	PCS		2/5			C	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0033725	PMID:35240055	PCS		1/3			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0008770	PMID:35240055	PCS		1/4			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0002917	PMID:35240055	PCS		1/4			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0001629	PMID:35240055	PCS		1/5			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0011463	PMID:35240055	PCS		3/5			C	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0000729	PMID:35240055	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0002506	PMID:35240055	PCS		1/3			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0000007	PMID:35240055	PCS					I	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0000821	PMID:35240055	PCS		3/4			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0003429	PMID:35240055	PCS		1/3			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0007018	PMID:35240055	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0001510	PMID:35240055	PCS		1/5			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0001249	PMID:35240055	PCS		4/4			P	HPO:probinson[2022-08-17]
OMIM:619908	Neurodevelopmental disorder with language delay and seizure		HP:0000028	PMID:35240055	PCS		2/4			P	HPO:probinson[2022-08-17]
OMIM:610092	Microphthalmia with coloboma 3		HP:0000518	PMID:10932181	PCS	HP:0003577				P	HPO:probinson[2013-03-31];HPO:probinson[2020-07-24]
OMIM:610092	Microphthalmia with coloboma 3		HP:0000568	PMID:10932181	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-24]
OMIM:610092	Microphthalmia with coloboma 3		HP:0000007	PMID:15257456	PCS					I	HPO:probinson[2013-03-31];HPO:probinson[2020-07-24]
OMIM:610092	Microphthalmia with coloboma 3		HP:0000612	PMID:15257456	PCS					P	HPO:probinson[2020-07-24]
OMIM:620151	Wolman disease		HP:0002013	PMID:21963785	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0001508	PMID:21963785;PMID:8146180	PCS		3/3			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0002240	PMID:21963785;PMID:8146180	PCS		3/3			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0003593	PMID:21963785;PMID:8146180	PCS		3/3			C	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0000007	PMID:8146180	PCS					I	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0003270	PMID:21963785	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0006554	PMID:21963785	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0001945	PMID:21963785	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0001522	PMID:21963785;PMID:8146180	PCS		3/3			C	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0031205	PMID:8617513	PCS		2/2			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0001744	PMID:21963785;PMID:8146180	PCS		3/3			P	HPO:probinson[2024-03-01]
OMIM:620151	Wolman disease		HP:0010512	PMID:21963785;PMID:8146180	PCS		3/3			P	HPO:probinson[2024-03-01]
OMIM:168400	Parastremmatic dwarfism		HP:0003510	PMID:4992387	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0002650	PMID:4992387	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0001371	PMID:4992387	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0002808	PMID:4992387	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0000470	PMID:4992387	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0003593	PMID:4992387	PCS		3/3			C	HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0006487	PMID:4992387	PCS		3/3			P	HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0002857	PMID:4992387	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0000006	PMID:20503319	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:168400	Parastremmatic dwarfism		HP:0001249	PMID:4992387	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-21]
OMIM:608805	Avascular necrosis of femoral head, primary, 1		HP:0005743	PMID:15930420;PMID:21671384	PCS		11/11			P	HPO:probinson[2022-06-18];HPO:skoehler[2013-01-09];HPO:probinson[2022-06-18]
OMIM:608805	Avascular necrosis of femoral head, primary, 1		HP:0025708	PMID:15930420;PMID:21671384	PCS		2/2			C	HPO:probinson[2022-06-18]
OMIM:608805	Avascular necrosis of femoral head, primary, 1		HP:0040160	PMID:21671384	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:608805	Avascular necrosis of femoral head, primary, 1		HP:0031520	PMID:15930420	PCS		1/1			P	HPO:probinson[2022-06-18];HPO:probinson[2022-07-10]
OMIM:608805	Avascular necrosis of femoral head, primary, 1		HP:0030838	PMID:21671384	PCS		1/1			P	HPO:probinson[2022-06-18]
OMIM:608805	Avascular necrosis of femoral head, primary, 1		HP:0000006	PMID:15930420	PCS					I	HPO:skoehler[2013-03-25];HPO:probinson[2022-06-18]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0008749	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0003038	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04];HP:probinson[2018-07-14]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0002023	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0001674	PMID:27158779	PCS	HP:0003577	1/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0002089	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000260	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0003375	OMIM:617925	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0002162	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0001153	PMID:27158779	PCS	HP:0003577	1/2	FEMALE		P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0005474	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0410030	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0003173	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04];HP:probinson[2018-07-14]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0008551	OMIM:617925	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000316	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0100628	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000774	OMIM:617925	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0006610	OMIM:617925	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000773	OMIM:617925	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000377	OMIM:617925	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0003026	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000175	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000054	PMID:27158779	PCS	HP:0003577	1/1	MALE		P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000695	PMID:27158779	PCS	HP:0003577	1/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0003762	PMID:27158779	PCS	HP:0003577	1/1	FEMALE		P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000470	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0005285	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0011467	OMIM:617925	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0004491	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0011802	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0005280	OMIM:617925	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0100259	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0100258	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000888	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0001636	PMID:27158779	PCS	HP:0003577	1/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000007	PMID:27158779	PCS					I	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000568	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0100818	OMIM:617925	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0002007	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0003811	PMID:27158779	PCS		2/2			C	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0005736	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04];HP:probinson[2018-07-14]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000248	PMID:27158779	PCS	HP:0003577				P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000369	PMID:27158779	PCS	HP:0003577	2/2			P	HP:probinson[2018-07-04]
OMIM:617925	Short-Rib thoracic dysplasia 20 with polydactyly		HP:0000347	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:312300	Reifenstein syndrome		HP:0000054	OMIM:312300	IEA					P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0000771	PMID:1598912	PCS					P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0000051	PMID:1598912	PCS		5/5			P	HP:probinson[2018-04-15]
OMIM:312300	Reifenstein syndrome		HP:0001419	PMID:1598912	PCS					I	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0000789	OMIM:312300	IEA					P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0001547	OMIM:312300	IEA					P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0000037	OMIM:312300	IEA					P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0000048	OMIM:312300	IEA					P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0012873	OMIM:312300	TAS					P	HPO:skoehler[2014-06-24]
OMIM:312300	Reifenstein syndrome		HP:0000135	OMIM:312300	IEA					P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0000028	PMID:1598912	PCS		5/5			P	HPO:iea[2009-02-17]
OMIM:312300	Reifenstein syndrome		HP:0000027	OMIM:312300	IEA					P	HPO:iea[2009-02-17]
OMIM:125500	Dentinogenesis imperfecta, shields type III		HP:0000694	OMIM:125500	IEA					P	HPO:iea[2009-02-17]
OMIM:125500	Dentinogenesis imperfecta, shields type III		HP:0009102	PMID:6579461	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-07]
OMIM:125500	Dentinogenesis imperfecta, shields type III		HP:0000700	PMID:6579461	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-07]
OMIM:125500	Dentinogenesis imperfecta, shields type III		HP:0000703	PMID:6579461	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2021-05-07]
OMIM:125500	Dentinogenesis imperfecta, shields type III		HP:0009722	PMID:6579461	PCS					P	HPO:probinson[2021-05-07]
OMIM:125500	Dentinogenesis imperfecta, shields type III		HP:0000006	OMIM:125500	IEA					I	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0000286	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0002188	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0002265	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0000343	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0000541	PMID:25093588	PCS		2/10			P	HPO:probinson[2024-03-09]
OMIM:249310	Neuhauser syndrome		HP:0000485	PMID:25093588	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:249310	Neuhauser syndrome		HP:0004322	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0002120	OMIM:249310	IEA					P	HPO:skoehler[2018-10-08]
OMIM:249310	Neuhauser syndrome		HP:0001250	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0012805	PMID:25093588	PCS		5/10			P	HPO:probinson[2024-03-09]
OMIM:249310	Neuhauser syndrome		HP:0001252	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0001251	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0001290	OMIM:249310	TAS					P	HPO:skoehler[2017-07-13]
OMIM:249310	Neuhauser syndrome		HP:0100693	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0002816	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0000938	OMIM:249310	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249310	Neuhauser syndrome		HP:0000316	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0000832	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0002857	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0000218	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0000378	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0000256	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0001763	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0000311	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0001249	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0001166	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0002311	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0000494	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0002015	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0000252	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0000431	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0003124	OMIM:249310	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249310	Neuhauser syndrome		HP:0000193	OMIM:249310	TAS					P	HPO:skoehler[2015-12-30]
OMIM:249310	Neuhauser syndrome		HP:0001084	PMID:25093588	PCS		3/10			P	HPO:probinson[2024-03-09]
OMIM:249310	Neuhauser syndrome		HP:0000294	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249310	Neuhauser syndrome		HP:0012632	PMID:25093588	PCS		0/10			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:249310	Neuhauser syndrome		HP:0005280	OMIM:249310	TAS					P	HPO:skoehler[2013-06-12]
OMIM:249310	Neuhauser syndrome		HP:0008081	OMIM:249310	TAS					P	HPO:skoehler[2017-07-13]
OMIM:249310	Neuhauser syndrome		HP:0000007	OMIM:249310	IEA					I	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0007676	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0002007	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0000347	OMIM:249310	IEA					P	HPO:iea[2009-02-17]
OMIM:249310	Neuhauser syndrome		HP:0000545	OMIM:249310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000286	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000483	PMID:22284827	PCS		3/27			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-28]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0007858	OMIM:152950	TAS		HP:0040283			P	HPO:skoehler[2015-07-19]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0007957	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000340	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000582	OMIM:152950	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000343	OMIM:152950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000541	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000463	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0002002	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000540	PMID:22284827	PCS		3/27			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-28]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000482	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0032794	PMID:22284827	PCS		1/27			P	HPO:probinson[2023-02-28]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0500041	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0008052	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000518	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000639	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000718	OMIM:152950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0011220	OMIM:152950	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0003828	OMIM:152950	IEA					M	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0003829	OMIM:152950	IEA					I	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0007663	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000219	OMIM:152950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000713	OMIM:152950	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000455	OMIM:152950	TAS					P	HPO:skoehler[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000411	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0001004	PMID:22284827	PCS		14/27			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000179	OMIM:152950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0005469	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000494	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000252	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0005280	OMIM:152950	IEA					P	HPO:iea[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000568	OMIM:152950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000648	OMIM:152950	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0007731	PMID:22284827	PCS		11/27			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-28]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0007018	OMIM:152950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000006	PMID:22284827	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000303	OMIM:152950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0000545	OMIM:152950	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:152950	Microcephaly with or without chorioretinopathy, lymphedema, or impaired intellectual development		HP:0009879	OMIM:152950	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0002421	PMID:15968592	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0001271	OMIM:609528	IEA					P	HPO:iea[2009-02-17]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0001252	OMIM:609528	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0003593	OMIM:609528;PMID:15968592	PCS		17/17			C	HPO:probinson[2021-05-30];HPO:iea[2009-02-17]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0001273	OMIM:609528	IEA					P	HPO:iea[2009-02-17]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0011951	PMID:15968592	PCS		3/7			P	HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0001508	PMID:15968592	PCS	HP:0003593	7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000316	PMID:15968592	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0002539	PMID:15968592	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0001302	PMID:15968592	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0007766	OMIM:609528	IEA					P	HPO:iea[2009-02-17]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000253	PMID:15968592	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000494	PMID:15968592	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000431	PMID:15968592	PCS		7/7			P	HPO:probinson[2012-05-01];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000276	PMID:15968592	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0001263	PMID:15968592	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0001284	PMID:15968592	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0005280	PMID:15968592	PCS		7/7			P	HPO:probinson[2012-05-01];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0008064	PMID:15968592	PCS	HP:0003593	7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0003819	PMID:15968592	PCS		3/7			C	HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000407	OMIM:609528	IEA					P	HPO:iea[2009-02-17]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0009830	OMIM:609528	TAS					P	HPO:probinson[2009-02-17]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000007	PMID:15968592	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0000982	PMID:15968592	PCS	HP:0003593	7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-30]
OMIM:609528	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome		HP:0002126	PMID:15968592	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-05-30]
OMIM:167900	Papillomatosis, familial cutaneous		HP:0000006	OMIM:167900	TAS					I	HPO:probinson[2009-02-17]
OMIM:167900	Papillomatosis, familial cutaneous		HP:0000962	OMIM:167900	TAS					P	HPO:probinson[2012-07-16]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0002069	PMID:8050626	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0010529	PMID:8050626	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0001250	OMIM:608636	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0001252	PMID:8050626	PCS	HP:0003593	1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0003593	PMID:8050626	PCS		1/1			C	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0011463	OMIM:608636	IEA					C	HPO:iea[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000817	PMID:8050626	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0003829	OMIM:608636	TAS					I	HPO:skoehler[2015-12-30]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000717	PMID:8050626	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000733	PMID:8050626	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0001426	OMIM:608636	IEA					I	HPO:iea[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000758	OMIM:608636	TAS					P	HPO:probinson[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0002317	PMID:8050626	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0003745	OMIM:608636	IEA					I	HPO:iea[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000732	PMID:8050626	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0001249	OMIM:608636	IEA					P	HPO:iea[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000750	PMID:8050626	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0002353	OMIM:608636	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0002078	PMID:8050626	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0003144	OMIM:608636	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0012760	PMID:8050626	PCS		1/1			P	HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000728	PMID:8050626	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000723	OMIM:608636	TAS					P	HPO:skoehler[2013-06-04]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000006	PMID:8050626	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-23]
OMIM:608636	Chromosome 15q11-q13 duplication syndrome		HP:0000721	OMIM:608636	IEA					P	HPO:iea[2009-02-17]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0002069	PMID:31036918	PCS		5/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0002487	PMID:31036918	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0000473	PMID:31036918	PCS		3/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0008936	PMID:31036918	PCS		1/7			P	HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0000750	PMID:31036918	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0001332	PMID:31036918	PCS		3/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0002395	PMID:31036918	PCS		1/7			P	HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0001263	PMID:31036918	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0001251	PMID:31036918	PCS		4/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0003593	PMID:31036918	PCS		5/7			C	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0002072	PMID:31036918	PCS		1/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0000007	PMID:31036918	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0025336	PMID:31036918	PCS		1/7			P	HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0000268	PMID:31036918	PCS		4/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0001337	PMID:31036918	PCS		4/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0001249	PMID:31036918	PCS		6/7			P	HPO:probinson[2023-01-30]
OMIM:618425	Neurodevelopmental disorder with impaired speech and hyperkinetic movements		HP:0003623	PMID:31036918	PCS		2/7			C	HPO:probinson[2023-01-30]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000582	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0003577	PMID:19455184	PCS		1/1			C	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002365	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000540	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0010648	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001250	OMIM:618343	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001075	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001270	OMIM:618343	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0030816	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000319	PMID:19455184	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000418	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002619	PMID:19455184	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002539	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002617	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0100807	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000678	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002119	PMID:19455184	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000978	OMIM:618343	IEA		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0025336	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000278	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001642	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001788	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000233	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001762	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000750	OMIM:618343	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000430	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000276	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0031936	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001321	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000496	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001382	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000490	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002350	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0011147	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0012385	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000987	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000007	PMID:19455184	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002647	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000322	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001238	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0002126	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0000347	OMIM:618343	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618343	Polymicrogyria with or without vascular-type EDS		HP:0001776	PMID:19455184	PCS		1/1			P	HPO:probinson[2022-10-10]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0001265	PMID:23043144	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003477	PMID:23043144	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003202	PMID:23043144	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0002015	PMID:23043144	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003236	PMID:23043144	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003200	PMID:23043144	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003596	PMID:23043144	PCS		4/6			C	HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003201	PMID:23043144	PCS		1/6			P	HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0002120	PMID:23043144	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0000590	PMID:23043144	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003584	PMID:23043144	PCS		1/6			C	HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0002151	PMID:23043144	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0002460	PMID:23043144	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0001618	PMID:23043144	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0000407	PMID:23043144	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0000726	PMID:23043144	PCS		1/6			P	HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0011462	PMID:23043144	PCS		1/6			C	HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0000508	PMID:23043144	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0000007	PMID:23043144	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003701	PMID:23043144	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003688	PMID:23043144	PCS		6/6			P	HPO:probinson[2023-03-28]
OMIM:617070	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4		HP:0003689	PMID:23043144	PCS		6/6			P	HPO:probinson[2023-03-28]
OMIM:235740	Hirschsprung disease with polydactyly, renal agenesis, and deafness		HP:0000365	OMIM:235740	IEA					P	HPO:iea[2009-02-17]
OMIM:235740	Hirschsprung disease with polydactyly, renal agenesis, and deafness		HP:0000122	OMIM:235740	IEA					P	HPO:iea[2009-02-17]
OMIM:235740	Hirschsprung disease with polydactyly, renal agenesis, and deafness		HP:0001161	OMIM:235740	IEA					P	HPO:iea[2009-02-17]
OMIM:235740	Hirschsprung disease with polydactyly, renal agenesis, and deafness		HP:0002251	OMIM:235740	IEA					P	HPO:iea[2009-02-17]
OMIM:235740	Hirschsprung disease with polydactyly, renal agenesis, and deafness		HP:0000316	OMIM:235740	IEA					P	HPO:iea[2009-02-17]
OMIM:235740	Hirschsprung disease with polydactyly, renal agenesis, and deafness		HP:0000007	OMIM:235740	IEA					I	HPO:iea[2009-02-17]
OMIM:179280	Radial-Renal syndrome		HP:0004322	PMID:6829604	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:179280	Radial-Renal syndrome		HP:0000122	PMID:6829604	PCS		1/2			P	HPO:probinson[2020-09-13]
OMIM:179280	Radial-Renal syndrome		HP:0000086	PMID:6829604	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-09-13]
OMIM:179280	Radial-Renal syndrome		HP:0040012	PMID:6829604	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-13]
OMIM:179280	Radial-Renal syndrome		HP:0009777	PMID:6829604	PCS		2/2		HP:0012832	P	HPO:probinson[2012-06-03];HPO:probinson[2020-09-13]
OMIM:179280	Radial-Renal syndrome		HP:0000377	PMID:6829604	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:179280	Radial-Renal syndrome		HP:0000006	PMID:6829604	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:179280	Radial-Renal syndrome		HP:0003974	PMID:6829604	PCS		2/2		HP:0012832	P	HPO:probinson[2012-06-03];HPO:probinson[2020-09-13]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0001671	OMIM:601612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0003577	OMIM:601612	TAS					C	HPO:skoehler[2012-10-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0001680	OMIM:601612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0000007	OMIM:601612	IEA					I	HPO:iea[2009-02-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0030680	OMIM:601612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0002093	OMIM:601612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0003811	OMIM:601612	IEA					C	HPO:iea[2009-02-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0001643	OMIM:601612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0005944	OMIM:601612	IEA					P	HPO:iea[2009-02-17]
OMIM:601612	Lung agenesis, congenital heart defects, and thumb anomalies syndrome		HP:0100682	OMIM:601612	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0000594	PMID:3827713	PCS	HP:0011463				P	HP:probinson[2018-05-03]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0001133	PMID:3827713	PCS					P	HP:probinson[2018-05-03]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0000662	PMID:3827713	PCS					P	HPO:skoehler[2012-10-17]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0000540	PMID:3827713	PCS					P	HP:probinson[2018-05-03]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0000007	OMIM:267760	IEA					I	HPO:iea[2009-02-17]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0000568	PMID:3827713	PCS					P	HPO:skoehler[2013-04-02]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0000546	PMID:3827713	IEA					P	HPO:skoehler[2015-01-27]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0008028	OMIM:267760	IEA					P	HPO:iea[2009-02-17]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0007401	PMID:3827713	PCS	HP:0003581				P	HPO:skoehler[2015-07-26]
OMIM:267760	Retinal degeneration with nanophthalmos, cystic macular degeneration,and angle closure glaucoma		HP:0000501	OMIM:267760	IEA					P	HPO:iea[2009-02-17]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0001000	PMID:19878917	PCS		0/6			P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-24];HPO:probinson[2024-03-14]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0000486	PMID:19896113	PCS		2/5			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2024-03-14]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0000639	PMID:19896109	PCS		4/6			P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-24]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0000958	PMID:19878917	PCS		3/6			P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-24];HPO:probinson[2024-03-14]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0007663	PMID:19896109	PCS		6/6			P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-24]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0000007	PMID:19896109	PCS					I	HPO:nvasilevsky[2019-02-25];HPO:probinson[2020-07-24]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0007642	PMID:19896109	PCS		6/6			P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-24]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0000545	PMID:19896109	PCS		5/6			P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-24]
OMIM:613216	Night blindness, congenital stationary (complete), 1C, autosomal recessive		HP:0000512	PMID:19878917	PCS		1/1			P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-24];HPO:probinson[2024-03-14]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0003279	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000684	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0004322	PMID:36467473	PCS		3/3			P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0004363	PMID:36467473	PCS		0/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001290	OMIM:190350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0010049	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0045074	OMIM:190350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0010252	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0100529	PMID:36467473	PCS		0/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0003307	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001763	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002217	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001249	PMID:36467473	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0004379	PMID:36467473	PCS		0/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0005743	OMIM:190350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002750	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000691	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002829	OMIM:190350	TAS	HP:0003584				P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001816	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000689	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000447	OMIM:190350	TAS					P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000768	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000400	OMIM:190350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000006	PMID:10615131	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0005338	OMIM:190350	TAS					P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0008947	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000343	PMID:36467473	PCS		2/2			P	HPO:probinson[2012-05-01];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000189	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001156	PMID:36467473	PCS		3/3			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002002	OMIM:190350	TAS					P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0003691	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0003370	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0010300	OMIM:190350	TAS					P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0010743	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0010270	OMIM:190350	TAS					P	HPO:probinson[2012-06-10]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000938	OMIM:190350	TAS	HP:0003584				P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0006253	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000414	PMID:36467473	PCS		3/3			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000219	PMID:36467473	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0030084	PMID:36467473	PCS		1/2			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002758	OMIM:190350	TAS	HP:0003584				P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000411	PMID:36467473	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001820	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000670	OMIM:190350	TAS					P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002213	OMIM:190350	PCS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002650	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0011823	OMIM:190350	TAS					P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0010259	OMIM:190350	TAS					P	HPO:probinson[2012-06-10]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002805	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002209	PMID:36467473	PCS		3/3			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0002205	OMIM:190350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001598	OMIM:190350	TAS					P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0001510	OMIM:190350	TAS				HP:0012825	P	HPO:probinson[2012-07-29]
OMIM:190350	Trichorhinophalangeal syndrome, type I		HP:0000347	OMIM:190350	TAS					P	HPO:probinson[2009-02-17]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000286	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0003477	PMID:24336167	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0003236	PMID:29721912	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0010804	PMID:29721912	PCS		1/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001332	PMID:29721912;PMID:24336167	PCS		13/28			P	HPO:probinson[2021-10-18];HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001250	PMID:29721912;PMID:32395406	PCS		5/14			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001252	PMID:29721912	PCS		6/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0003394	PMID:29721912	PCS		4/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001251	PMID:32395406	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0003391	PMID:29721912	PCS		1/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000316	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001328	PMID:24336167	PCS		15/15			P	HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000752	PMID:29721912	PCS		2/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0003701	PMID:24336167	PCS		15/15			P	HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002312	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000252	PMID:24336167	PCS		5/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001266	PMID:29721912	PCS		1/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002310	PMID:24336167	PCS		10/15			P	HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001382	PMID:29721912	PCS		1/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001263	PMID:29721912;PMID:32395406	PCS		14/14			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002072	PMID:24336167	PCS		10/15			P	HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002071	PMID:29721912;PMID:24336167	PCS		15/28			P	HPO:probinson[2021-10-18];HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0010910	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0007033	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000646	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000007	PMID:24336167	PCS					I	HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000648	PMID:24336167	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001337	PMID:24336167	PCS		10/15			P	HPO:probinson[2015-05-10]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001974	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002169	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000463	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0030235	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002240	PMID:29721912	PCS		2/8			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002161	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001270	PMID:29721912	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0012650	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001629	PMID:29721912	PCS		2/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0040197	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0009046	PMID:24336167	PCS		7/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002359	PMID:29721912	PCS		2/8			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001027	PMID:29721912	PCS		1/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002910	PMID:29721912	PCS		12/12			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001744	PMID:29721912	PCS		1/8			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000275	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000750	PMID:29721912;PMID:32395406	PCS		11/11			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002133	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001288	PMID:29721912	PCS		4/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0003388	PMID:29721912	PCS		1/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000470	PMID:29721912	PCS		1/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0034051	PMID:32395406	PCS		1/1			P	HPO:probinson[2022-02-05]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0008981	PMID:29721912	PCS		3/13			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0000508	PMID:24336167	PCS		2/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0002922	PMID:32395406	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:615673	Myopathy with extrapyramidal signs		HP:0001510	PMID:29721912	PCS		4/10			P	HPO:probinson[2021-10-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0002069	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0003621	PMID:27352968	PCS		8/20			C	HPO:probinson[2022-10-12]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0000992	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0000750	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0025097	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0001250	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0002121	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0001263	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0003593	PMID:27352968	PCS		1/20			C	HPO:probinson[2022-10-12]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0000708	OMIM:618357	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0011463	PMID:27352968	PCS		11/20			C	HPO:probinson[2022-10-12]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0000718	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0003829	OMIM:618357	IEA					I	HPO:skoehler[2019-04-18]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0000006	PMID:27352968	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-12]
OMIM:618357	Epilepsy, idiopathic generalized, susceptibility to, 15		HP:0001336	OMIM:618357	IEA					P	HPO:skoehler[2019-04-18]
OMIM:275370	Tricarboxylic acid cycle, defect of		HP:0002928	OMIM:275370	IEA					P	HPO:iea[2009-02-17]
OMIM:275370	Tricarboxylic acid cycle, defect of		HP:0000707	OMIM:275370	IEA					P	HPO:iea[2009-02-17]
OMIM:275370	Tricarboxylic acid cycle, defect of		HP:0000007	OMIM:275370	IEA					I	HPO:iea[2009-02-17]
OMIM:275370	Tricarboxylic acid cycle, defect of		HP:0004898	OMIM:275370	IEA					P	HPO:iea[2009-02-17]
OMIM:601606	Trichoepithelioma, multiple familial, 1		HP:0002671	OMIM:601606	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:601606	Trichoepithelioma, multiple familial, 1		HP:0003581	OMIM:601606	IEA					C	HPO:iea[2009-02-17]
OMIM:601606	Trichoepithelioma, multiple familial, 1		HP:0000006	OMIM:601606	IEA					I	HPO:iea[2009-02-17]
OMIM:300923	Intellectual developmental disorder, X-linked 100		HP:0002069	PMID:24812067	PCS	HP:0003621	4/5			P	HPO:probinson[2021-09-26]
OMIM:300923	Intellectual developmental disorder, X-linked 100		HP:0000750	PMID:24812067	PCS		5/5			P	HPO:probinson[2021-09-26]
OMIM:300923	Intellectual developmental disorder, X-linked 100		HP:0001419	PMID:24812067	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-09-26]
OMIM:300923	Intellectual developmental disorder, X-linked 100		HP:0002121	PMID:24812067	PCS	HP:0003621	4/5			P	HPO:probinson[2021-09-26]
OMIM:300923	Intellectual developmental disorder, X-linked 100		HP:0001999	PMID:24812067	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-26]
OMIM:300923	Intellectual developmental disorder, X-linked 100		HP:0001249	PMID:24812067	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-26]
OMIM:618431	Hydatidiform mole, recurrent, 3		HP:0032192	PMID:30388401	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:618431	Hydatidiform mole, recurrent, 3		HP:0008222	PMID:30388401	PCS		2/2			P	HPO:probinson[2022-11-07]
OMIM:618431	Hydatidiform mole, recurrent, 3		HP:0011462	PMID:30388401	PCS		2/2			C	HPO:probinson[2022-11-07]
OMIM:618431	Hydatidiform mole, recurrent, 3		HP:0000007	PMID:30388401	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-07]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000340	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0003577	PMID:8151644	PCS		1/1			C	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000463	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0002066	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000160	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000581	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0003593	PMID:8411037	PCS		1/1			C	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0005274	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000718	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0009882	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000239	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0007663	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000219	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0008897	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000218	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0006895	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0001466	PMID:8411037	PCS					I	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000358	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0002553	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000494	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000431	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0011968	PMID:8151644;PMID:8411037	PCS		2/2			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0001263	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000470	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0040025	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000506	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000508	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0008743	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0009237	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000405	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0001511	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0001873	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000322	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000347	PMID:8411037	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000369	PMID:8151644;PMID:8411037	PCS		2/2			P	HPO:probinson[2024-05-08]
OMIM:613564	Chromosome 2p12-p11.2 deletion syndrome		HP:0000028	PMID:8151644	PCS		1/1			P	HPO:probinson[2024-05-08]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0001287	PMID:33951726	PCS		1/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0002850	PMID:33951726	PCS		6/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0003577	PMID:33951726	PCS		5/5			C	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0410255	PMID:33951726	PCS		1/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0004432	PMID:33951726	PCS		6/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0030252	PMID:33951726	PCS		6/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0002205	PMID:33951726	PCS		6/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0100651	PMID:33951726	PCS	HP:0011463	1/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0011108	PMID:33951726	PCS		6/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0000006	PMID:33951726	PCS					I	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0002720	PMID:33951726	PCS		6/6			P	HPO:probinson[2022-03-05]
OMIM:619707	Agammaglobulinemia 10, autosomal dominant		HP:0004315	PMID:33951726	PCS					P	HPO:probinson[2022-03-05]
OMIM:607539	Camptosynpolydactyly, complex		HP:0012385	PMID:27041388	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-14]
OMIM:607539	Camptosynpolydactyly, complex		HP:0001792	OMIM:607539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607539	Camptosynpolydactyly, complex		HP:0003577	PMID:27041388	PCS		1/1			C	HPO:probinson[2022-12-14]
OMIM:607539	Camptosynpolydactyly, complex		HP:0100797	PMID:27041388	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-14]
OMIM:607539	Camptosynpolydactyly, complex		HP:0002164	OMIM:607539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607539	Camptosynpolydactyly, complex		HP:0000007	PMID:27041388	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-14]
OMIM:607539	Camptosynpolydactyly, complex		HP:0012725	OMIM:607539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607539	Camptosynpolydactyly, complex		HP:0010442	PMID:27041388	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-14]
OMIM:607539	Camptosynpolydactyly, complex		HP:0001159	PMID:27041388	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-14]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000286	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0004322	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002020	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0045075	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0010055	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0011220	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0010296	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000316	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000954	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000494	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000695	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002474	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000453	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000452	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0011800	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0008282	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0034197	PMID:31949313	PCS		1/9			C	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000408	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0034199	PMID:31949313	PCS		1/9			C	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0034198	PMID:31949313	PCS		1/9			C	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000646	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000568	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000405	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0008404	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002943	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000289	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000006	PMID:31949313	PCS					I	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000369	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000324	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0001655	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0005359	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0001792	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0004467	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0010628	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002561	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0005990	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0010943	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0008070	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0008551	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000414	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000612	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000219	PMID:31949313	PCS		3/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0030084	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0009765	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002714	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002557	PMID:31949313	PCS		3/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000851	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000410	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0008513	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0006579	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000413	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0001667	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000275	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000396	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0001561	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000670	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0007925	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000750	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000431	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000430	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000034	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000193	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002092	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0005280	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0009796	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000348	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000821	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0002205	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0001511	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000268	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0001631	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000347	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0000588	PMID:31949313	PCS		1/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0008625	PMID:31949313	PCS		2/9			P	HPO:probinson[2023-06-11]
OMIM:620186	Branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome		HP:0004502	PMID:31949313	PCS		4/9			P	HPO:probinson[2023-06-11]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000286	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002221	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002023	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001377	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0004322	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000122	PMID:30893644	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002021	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0045075	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000958	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000319	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000954	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000510	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001169	PMID:30893644	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000358	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001540	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002553	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001385	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000013	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002750	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000133	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0011969	OMIM:618419	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0010554	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000407	PMID:30893644	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0040189	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000007	PMID:30893644	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001539	PMID:30893644	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0009611	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000444	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000369	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002225	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001853	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000341	PMID:30893644	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0003577	PMID:30893644	PCS		4/4			C	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000343	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001274	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000060	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0012368	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0008232	OMIM:618419	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001747	PMID:30893644	PCS		1/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000059	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002236	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000396	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0002650	PMID:30893644	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0004279	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000233	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000430	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0001518	PMID:30893644	PCS		2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0007892	PMID:30893644	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:618419	Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy		HP:0000668	PMID:30893644	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-05]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0001056	OMIM:226700	IEA					P	HPO:iea[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0003577	PMID:7698759	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0000670	OMIM:226700	IEA					P	HPO:iea[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0003341	PMID:7698759	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-12]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0002021	OMIM:226700	IEA					P	HPO:iea[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0002164	OMIM:226700	IEA					P	HPO:iea[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0001075	OMIM:226700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0001508	OMIM:226700	IEA					P	HPO:iea[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0007383	OMIM:226700	IEA					P	HPO:iea[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0008066	PMID:7698759	PCS		1/1			P	HP:probinson[2019-03-02];HPO:probinson[2022-05-12]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0006297	OMIM:226700	IEA					P	HPO:iea[2009-02-17]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0000007	PMID:7698759	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-12]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0001159	PMID:7698759	PCS		0/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-12]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0008404	OMIM:226700	TAS					P	HPO:skoehler[2013-05-03]
OMIM:226700	Epidermolysis bullosa, junctional, Herlitz type		HP:0001522	OMIM:226700	IEA					C	HPO:iea[2009-02-17]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0003236	PMID:25227914	PCS		5/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0003324	PMID:25227914	PCS		5/6			P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0003621	PMID:25227914	PCS		1/5			C	HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0011463	PMID:25227914	PCS		4/5			C	HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0000616	PMID:24591628	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0009027	OMIM:615883	TAS					P	HPO:skoehler[2015-04-19]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0002527	OMIM:615883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0002901	PMID:25227914	PCS		5/5			P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0006466	PMID:25227914	PCS		5/5			P	HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0001324	PMID:24591628	PCS		2/2		HP:0012840	P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0003701	PMID:25227914	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0003306	PMID:25227914	PCS		6/6			P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0002522	OMIM:615883	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0000006	PMID:24591628	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0003677	PMID:25227914	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-20]
OMIM:615883	Myopathy, tubular aggregate, 2		HP:0000467	OMIM:615883	IEA					P	HPO:skoehler[2019-04-18]
OMIM:620838	Spermatogenic failure 91		HP:0033393	PMID:36546111	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:620838	Spermatogenic failure 91		HP:0034011	PMID:36546111;PMID:36527329	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:620838	Spermatogenic failure 91		HP:0003251	PMID:36546111;PMID:31985809;PMID:36527329	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:620838	Spermatogenic failure 91		HP:0011462	PMID:36546111;PMID:31985809;PMID:36527329	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:620838	Spermatogenic failure 91		HP:0012207	PMID:36546111;PMID:36527329	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:620838	Spermatogenic failure 91		HP:0000007	PMID:31985809	PCS					I	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:620838	Spermatogenic failure 91		HP:0000798	PMID:36546111;PMID:31985809	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:620838	Spermatogenic failure 91		HP:0012205	PMID:36546111;PMID:31985809	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-08-02]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0000750	PMID:25175347	PCS		1/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0002376	PMID:25175347	PCS		5/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0001250	PMID:25175347	PCS		2/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0001260	PMID:25175347	PCS		2/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0001285	PMID:25175347	PCS		5/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0001251	PMID:25175347	PCS		2/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0033369	PMID:25175347	PCS		6/6			P	HPO:probinson[2021-02-13]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0007141	PMID:25175347	PCS		3/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0011463	PMID:25175347	PCS		6/6			C	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0000007	PMID:25175347	PCS					I	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0008347	PMID:25175347	PCS		6/6			P	HPO:probinson[2020-12-07];HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0001249	PMID:25175347	PCS		3/6			P	HPO:probinson[2020-12-07]
OMIM:619061	Mitochondrial complex IV deficiency, nuclear type 17		HP:0003688	PMID:25175347	PCS					P	HPO:probinson[2020-12-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0002069	PMID:25262651	PCS		2/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0002521	PMID:25262651	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0001344	PMID:25262651	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0002540	PMID:25262651	PCS		4/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0002376	PMID:25262651	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0001288	PMID:25262651	PCS		1/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0002384	PMID:25262651	PCS		2/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0010819	PMID:25262651	PCS		2/10			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0001263	PMID:25262651	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0001252	PMID:25262651	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0003593	PMID:25262651	PCS		5/5			C	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0001290	PMID:25262651	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0032794	PMID:25262651	PCS		1/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0011097	PMID:25262651	PCS		5/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0007270	PMID:25262651	PCS		3/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0011151	PMID:25262651	PCS		2/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0032792	PMID:25262651	PCS		3/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0002506	PMID:25262651	PCS		2/5			P	HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0200134	PMID:25262651	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0100716	PMID:25262651	PCS		2/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0000006	PMID:25262651	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-07]
OMIM:616346	Epileptic encephalopathy, early infantile, 31		HP:0001249	PMID:25262651	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-07]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0002223	PMID:30239107;PMID:30475435	PCS		5/5			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001792	PMID:30475435	PCS		2/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0004488	PMID:30475435	PCS	HP:0011461	1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000581	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001290	PMID:30475435	PCS		3/3			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0002061	PMID:30239107	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000958	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000718	PMID:30475435	PCS		1/3			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000316	PMID:30475435	PCS		4/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001943	PMID:30239107	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0008872	PMID:30239107	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000219	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000218	PMID:30239107	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000653	PMID:30475435	PCS		4/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000378	PMID:30239107	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0002514	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000256	PMID:30239107	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0007109	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0007109	PMID:30239107	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001561	PMID:30239107;PMID:30475435	PCS	HP:0011461	4/5			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000494	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001520	PMID:30475435	PCS	HP:0003577	1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000750	PMID:30475435	PCS		3/3			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0031936	PMID:30475435	PCS		3/3			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000490	PMID:30475435	PCS		2/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001263	PMID:30239107;PMID:30475435	PCS		4/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0002195	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0012520	PMID:30475435	PCS		3/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0032152	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0032471	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000407	PMID:30239107	PCS		1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0002904	PMID:30239107	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000508	PMID:30475435	PCS		2/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0002209	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001558	PMID:30239107;PMID:30475435	PCS	HP:0011461	2/5			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000348	PMID:30475435	PCS		4/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0001319	PMID:30239107	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0004209	PMID:30475435	PCS		1/4			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0007018	PMID:30475435	PCS		2/3			P	HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000006	PMID:30475435	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619075	Neurodevelopmental disorder with alopecia and brain abnormalities		HP:0000028	PMID:30475435	PCS		2/3	MALE		P	HPO:probinson[2020-12-05]
OMIM:615897	Immunodeficiency 24		HP:0005523	PMID:32161190	PCS		1/5			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0410297	PMID:32161190	PCS		3/4			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0011947	PMID:32161190	PCS		3/5			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0030374	PMID:32161190	PCS		5/5			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0031379	PMID:24870241	PCS		1/4			P	HPO:probinson[2015-03-28];HP:probinson[2019-01-26]
OMIM:615897	Immunodeficiency 24		HP:0032248	PMID:32161190	PCS		1/5			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0031402	PMID:32161190	PCS		3/3			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0032170	PMID:32161190	PCS		3/5			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:4000039	PMID:32161190	PCS		5/5			P	HPO:probinson[2021-06-13]
OMIM:615897	Immunodeficiency 24		HP:0012476	PMID:32161190	PCS		4/4			P	HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0031691	PMID:24870241	PCS					P	HP:probinson[2019-01-26]
OMIM:615897	Immunodeficiency 24		HP:0033222	PMID:32161190	PCS		2/5			P	HPO:probinson[2020-12-07]
OMIM:615897	Immunodeficiency 24		HP:0000007	PMID:24870241	PCS					I	HPO:probinson[2015-03-28]
OMIM:615897	Immunodeficiency 24		HP:0001888	PMID:24870241	PCS					P	HPO:probinson[2015-03-28]
OMIM:615897	Immunodeficiency 24		HP:0004429	PMID:24870241	PCS		8/8			P	HP:probinson[2019-01-26];HP:probinson[2019-01-26]
OMIM:615897	Immunodeficiency 24		HP:0008348	PMID:24870241	PCS		3/3			P	HPO:probinson[2015-03-28];HP:probinson[2019-01-26]
OMIM:615897	Immunodeficiency 24		HP:0002721	PMID:32161190	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-21]
OMIM:615897	Immunodeficiency 24		HP:0004315	PMID:32161190	PCS		4/5			P	HPO:probinson[2020-10-21]
OMIM:614237	Hypotrichosis 9		HP:0000164	PMID:20054564	PCS		0/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:614237	Hypotrichosis 9		HP:0001597	PMID:20054564	PCS		0/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:614237	Hypotrichosis 9		HP:0000364	PMID:20054564	PCS		0/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:614237	Hypotrichosis 9		HP:0002231	PMID:20054564	PCS		4/4			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:614237	Hypotrichosis 9		HP:0002209	PMID:20054564	PCS		4/4			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:614237	Hypotrichosis 9		HP:0000007	PMID:20054564	PCS					I	HP:probinson[2019-03-02]
OMIM:614237	Hypotrichosis 9		HP:0000966	PMID:20054564	PCS		0/4			P	HPO:probinson[2024-03-15]
OMIM:614237	Hypotrichosis 9		HP:0000499	PMID:20054564	PCS		0/4			P	HPO:skoehler[2018-10-08];HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:614237	Hypotrichosis 9		HP:0045075	PMID:20054564	PCS		0/4			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-15]
OMIM:115400	Carpal displacement		HP:0000924	OMIM:115400	IEA					P	HPO:iea[2009-02-17]
OMIM:115400	Carpal displacement		HP:0000006	OMIM:115400	IEA					I	HPO:iea[2009-02-17]
OMIM:613558	Deafness, autosomal dominant 51		HP:0003676	PMID:20602916	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:613558	Deafness, autosomal dominant 51		HP:0000365	PMID:20602916	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-07]
OMIM:613558	Deafness, autosomal dominant 51		HP:0025710	PMID:20602916	PCS					C	HPO:probinson[2022-10-07]
OMIM:613558	Deafness, autosomal dominant 51		HP:0000006	PMID:20602916	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0002487	OMIM:616420	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000341	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0009739	PMID:25865492	PCS		1/4			P	HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0003676	OMIM:616420	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000582	PMID:25865492	PCS		1/4			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000365	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0002540	PMID:25865492	PCS		4/4			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000343	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000463	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0002365	PMID:25865492	PCS		4/4			P	HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0002120	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0001250	OMIM:616420	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0003196	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0001508	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000639	OMIM:616420	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000319	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000414	PMID:25865492	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0003429	PMID:25865492	PCS		4/4			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0002415	PMID:25865492	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0001347	OMIM:616420	TAS					P	HPO:skoehler[2015-07-05]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000577	PMID:25865492	PCS		1/4			P	HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0001166	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0008936	OMIM:616420	TAS					P	HPO:skoehler[2015-07-05]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0003202	PMID:25865492	PCS		4/4			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0002059	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000494	PMID:25865492	PCS		2/4			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0001344	OMIM:616420	TAS					P	HPO:skoehler[2015-07-05]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000233	PMID:25865492	PCS		2/4			P	HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0003487	OMIM:616420	TAS					P	HPO:skoehler[2015-07-05]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0002079	PMID:25865492	PCS		4/4			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0001263	PMID:25865492	PCS		4/4		HP:0012828	P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000272	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0005484	PMID:25865492	PCS		4/4			P	HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0034295	PMID:25865492	PCS		4/4			P	HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0011231	PMID:25865492	PCS		2/4			P	HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000007	PMID:25865492	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0001257	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000369	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616420	Leukodystrophy, hypomyelinating, 10		HP:0000325	OMIM:616420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0003236	OMIM:609500	TAS					P	HPO:iea[2009-02-17]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0003198	OMIM:609500	TAS					P	HPO:iea[2009-02-17]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0001639	OMIM:609500	TAS					P	HPO:iea[2009-02-17]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0001263	OMIM:609500	TAS					P	HPO:iea[2009-02-17]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0000007	OMIM:609500	TAS					I	HPO:iea[2009-02-17]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0001319	OMIM:609500	TAS					P	HPO:iea[2009-02-17]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0003736	OMIM:609500	TAS					P	HPO:iea[2009-02-17]
OMIM:609500	Myopathy, autophagic vacuolar, infantile-onset		HP:0003745	OMIM:609500	TAS					I	HPO:iea[2009-02-17]
OMIM:158500	Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus		HP:0000819	OMIM:158500	IEA					P	HPO:iea[2009-02-17]
OMIM:158500	Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus		HP:0003202	OMIM:158500	IEA					P	HPO:iea[2009-02-17]
OMIM:158500	Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus		HP:0001251	OMIM:158500	IEA					P	HPO:iea[2009-02-17]
OMIM:158500	Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus		HP:0000510	OMIM:158500	IEA					P	HPO:iea[2009-02-17]
OMIM:158500	Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus		HP:0000006	OMIM:158500	IEA					I	HPO:iea[2009-02-17]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000670	PMID:16501574	PCS		3/3			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000365	PMID:16501574	PCS		3/3			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0007925	PMID:28483234	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0001172	PMID:16501574	PCS		0/3			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000691	PMID:16501574;PMID:28483234	PCS		4/5			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0001092	PMID:28483234	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000509	PMID:16501574;PMID:28483234	PCS		5/5			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0008551	PMID:16501574;PMID:28483234	PCS		5/5			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000668	PMID:16501574;PMID:28483234	PCS		4/5			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0009942	PMID:28483234	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000378	PMID:16501574;PMID:28483234	PCS		5/5			P	HPO:probinson[2023-06-10];HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000564	PMID:28483234	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000006	PMID:16501574	PCS					I	HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000522	PMID:16501574	PCS		3/3			P	HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:620192	Lacrimoauriculodentodigital syndrome-2		HP:0000698	PMID:16501574	PCS		3/3			P	HPO:probinson[2023-06-10]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0007814	PMID:29198720	PCS		2/6			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0003577	PMID:29198720	PCS		3/6			C	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0500087	PMID:29198720	PCS		1/6			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0000639	PMID:29198720	PCS		2/6			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0011463	PMID:29198720	PCS		3/6			C	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0000407	PMID:29198720	PCS	HP:0003621	6/6			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0008499	PMID:29198720	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0000613	PMID:29198720	PCS		2/6			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0007663	PMID:29198720	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0000546	PMID:29198720	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:617879	Leber congenital amaurosis with early-onset deafness		HP:0000006	PMID:29198720	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001276	PMID:33473207	PCS		2/23			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0002069	PMID:33473207	PCS		5/23			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0010804	PMID:33473207	PCS		5/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0000463	PMID:33473207	PCS		8/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001250	PMID:33473207	PCS		17/23			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0002384	PMID:33473207	PCS		4/23			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0002121	PMID:33473207	PCS		5/23			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001252	PMID:33473207	PCS		21/23			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0003196	PMID:33473207	PCS		8/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0025162	PMID:33473207	PCS		7/19			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001847	PMID:33473207	PCS		5/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0000219	PMID:33473207	PCS		4/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0025336	PMID:33473207	PCS		21/23			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0012171	PMID:33473207	PCS		6/19			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0000179	PMID:33473207	PCS		4/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001249	PMID:33473207	PCS		20/20			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001344	PMID:33473207	PCS		16/21			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0000750	PMID:33473207	PCS		22/23			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0031936	PMID:33473207	PCS		20/20			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0011968	PMID:33473207	PCS		9/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001263	PMID:33473207	PCS		24/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001182	PMID:33473207	PCS		9/24			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0000729	PMID:33473207	PCS		7/21			P	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0000006	PMID:33473207	PCS					I	HPO:probinson[2022-08-07]
OMIM:619854	Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities		HP:0001513	PMID:33473207	PCS		7/24			P	HPO:probinson[2022-08-07]
OMIM:276902	Usher syndrome, type IIIA		HP:0003577	PMID:11524702	PCS		1/2			C	HPO:probinson[2022-08-15]
OMIM:276902	Usher syndrome, type IIIA		HP:0000662	OMIM:276902	TAS					P	HPO:probinson[2009-02-17]
OMIM:276902	Usher syndrome, type IIIA		HP:0001751	PMID:11524702	PCS		1/2			P	HPO:probinson[2012-03-09];HPO:probinson[2022-08-15]
OMIM:276902	Usher syndrome, type IIIA		HP:0001123	OMIM:276902	TAS		HP:0040282			P	HPO:probinson[2012-03-09]
OMIM:276902	Usher syndrome, type IIIA		HP:0000407	PMID:11524702	PCS		2/2			P	HPO:probinson[2012-03-09];HPO:probinson[2022-08-15]
OMIM:276902	Usher syndrome, type IIIA		HP:0011463	PMID:11524702	PCS		1/2			C	HPO:probinson[2022-08-15]
OMIM:276902	Usher syndrome, type IIIA		HP:0000007	PMID:11524702	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-15]
OMIM:276902	Usher syndrome, type IIIA		HP:0007663	PMID:11524702	PCS		2/2			P	HPO:probinson[2013-01-07];HPO:probinson[2022-08-15]
OMIM:276902	Usher syndrome, type IIIA		HP:0000510	PMID:11524702	PCS	HP:0003621	2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-15]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0003676	OMIM:604805	IEA					C	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0002166	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0000012	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0001761	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0003487	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0000020	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0002064	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0002061	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0011449	OMIM:604805	TAS					P	HPO:probinson[2012-04-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0011448	OMIM:604805	TAS					P	HPO:probinson[2012-04-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0007340	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0002839	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0001258	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0000006	OMIM:604805	IEA					I	HPO:iea[2009-02-17]
OMIM:604805	Spastic paraplegia 12, autosomal dominant		HP:0001347	OMIM:604805	IEA					P	HPO:iea[2009-02-17]
OMIM:122455	Coronary artery dissection, spontaneous		HP:0006702	OMIM:122455	IEA					P	HPO:iea[2009-02-17]
OMIM:122455	Coronary artery dissection, spontaneous		HP:0012180	OMIM:122455	TAS					P	HPO:probinson[2021-08-22]
OMIM:122455	Coronary artery dissection, spontaneous		HP:0000006	OMIM:122455	IEA					I	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002542	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003431	PMID:9448569	PCS		2/9			P	HPO:probinson[2012-04-18]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000640	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001252	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003394	PMID:14967775	PCS		3/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002460	PMID:14967775	PCS		2/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001290	OMIM:164400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002380	PMID:14967775	PCS		1/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000639	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000514	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0007006	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001324	PMID:14967775	PCS		1/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003701	PMID:14967775	PCS		1/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003744	OMIM:164400	IEA					I	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0007328	PMID:14967775	PCS		2/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003202	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003401	PMID:14967775	PCS		1/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002078	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003487	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0006937	PMID:14967775	PCS		2/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002198	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001260	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002075	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002072	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002073	PMID:14967775	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002070	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002071	OMIM:164400	PCS					P	HPO:probinson[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0010831	PMID:14967775	PCS		1/5			P	HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0007078	PMID:9448569	PCS		9/9			P	HPO:probinson[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000648	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000641	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001257	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002503	OMIM:164400	PCS					P	HPO:probinson[2012-03-12]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000006	PMID:7951322	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002168	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001310	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003693	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001151	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0100543	OMIM:164400	PCS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0007263	OMIM:164400	IEA					P	HPO:skoehler[2015-01-27]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002839	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003448	PMID:9448569	PCS		1/9			P	HPO:probinson[2012-04-18]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001347	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002015	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001283	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0002495	OMIM:164400;PMID:14967775	PCS		15/15			P	HPO:probinson[2021-07-04];HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0003581	PMID:14967775	PCS		6/6			C	HPO:probinson[2009-02-17];HPO:probinson[2021-07-04]
OMIM:164400	Spinocerebellar ataxia 1		HP:0001284	OMIM:164400	PCS					P	HPO:probinson[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0009830	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000623	OMIM:164400	IEA					P	HPO:iea[2009-02-17]
OMIM:164400	Spinocerebellar ataxia 1		HP:0000543	OMIM:164400	TAS					P	HPO:skoehler[2013-07-17]
OMIM:129500	Clouston syndrome		HP:0001155	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0000164	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0001792	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0007418	OMIM:129500	TAS			FEMALE		P	HPO:skoehler[2015-12-30]
OMIM:129500	Clouston syndrome		HP:0000486	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0002221	OMIM:129500	PCS					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0004322	OMIM:129500	PCS					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0001596	OMIM:129500	TAS					P	HPO:skoehler[2013-01-22]
OMIM:129500	Clouston syndrome		HP:0002164	OMIM:129500	PCS					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0045075	OMIM:129500	TAS					P	HPO:probinson[2022-05-08]
OMIM:129500	Clouston syndrome		HP:0000518	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0003828	OMIM:129500	TAS					M	HPO:skoehler[2013-01-22]
OMIM:129500	Clouston syndrome		HP:0001806	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0000613	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0000953	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0000653	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0000972	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0000498	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0002217	OMIM:129500	PCS					P	HPO:iea[2012-03-01]
OMIM:129500	Clouston syndrome		HP:0002555	OMIM:129500	PCS					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0001760	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0002213	OMIM:129500	PCS					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0002299	OMIM:129500	PCS					P	HPO:iea[2012-03-01]
OMIM:129500	Clouston syndrome		HP:0000968	OMIM:129500	IEA					P	HPO:skoehler[2015-01-14]
OMIM:129500	Clouston syndrome		HP:0000509	OMIM:129500	IEA					P	HPO:iea[2009-02-17]
OMIM:129500	Clouston syndrome		HP:0008404	OMIM:129500	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:129500	Clouston syndrome		HP:0000006	PMID:11017065	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0001531	PMID:27019227	PCS	HP:0003593	8/14			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0001531	PMID:15804299	PCS		2/2			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0012309	PMID:27019227	PCS					P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0002583	PMID:27019227	PCS		9/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0012227	PMID:27019227	PCS		5/14			P	HPO:skoehler[2013-04-02];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0033253	PMID:27019227	PCS					P	HPO:probinson[2020-12-07]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0011463	PMID:15804299	PCS		2/2			C	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0033178	PMID:27019227	PCS					P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0000613	PMID:15804299;PMID:2705473	PCS		12/12			P	HPO:probinson[2020-11-25];HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0000559	PMID:27019227	PCS		7/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0006532	PMID:27019227;PMID:15804299	PCS		12/12			P	HPO:probinson[2009-02-17];HPO:probinson[2020-11-25];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0007588	PMID:27019227;PMID:15804299	PCS		16/16			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0002236	PMID:27019227	PCS			MALE		P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0002236	PMID:15804299	PCS		2/2			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0001249	PMID:2705473	PCS		2/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0000572	PMID:2705473	PCS					P	HPO:probinson[2012-03-03];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0002110	PMID:27019227	PCS		13/14			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0001263	PMID:27019227	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0011229	PMID:27019227	PCS			MALE		P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0011229	PMID:15804299	PCS		2/2			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0001419	PMID:27019227	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0000965	PMID:27019227	PCS		3/14			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0001217	PMID:27019227	PCS		3/14			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0000505	PMID:2705473	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0007599	PMID:2705473	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0000966	PMID:27019227;PMID:15804299	PCS		11/16			P	HPO:probinson[2020-11-25];HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0002028	PMID:27019227	PCS		9/14			P	HPO:probinson[2020-11-25]
OMIM:301220	Pigmentary disorder, reticulate, with systemic manifestations, X-linked		HP:0000962	PMID:2705473	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-25]
OMIM:148840	Kleine-Levin hibernation syndrome		HP:0001289	OMIM:148840	IEA					P	HPO:iea[2009-02-17]
OMIM:148840	Kleine-Levin hibernation syndrome		HP:0006803	OMIM:148840	IEA					P	HPO:iea[2009-02-17]
OMIM:148840	Kleine-Levin hibernation syndrome		HP:0002591	OMIM:148840	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148840	Kleine-Levin hibernation syndrome		HP:0007200	OMIM:148840	IEA					P	HPO:iea[2009-02-17]
OMIM:148840	Kleine-Levin hibernation syndrome		HP:0000006	OMIM:148840	IEA					I	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0007957	PMID:15324318	PCS		28/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000365	PMID:15324318	PCS		15/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000684	PMID:15324318	PCS		16/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0003311	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0004322	PMID:15324318	PCS		28/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001371	PMID:15324318	PCS		28/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001250	PMID:15324318	PCS		5/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0003274	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0003593	PMID:15324318	PCS		16/25			C	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0010885	OMIM:253200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0010444	PMID:15324318	PCS		4/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000280	PMID:15324318	PCS		28/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001171	PMID:15324318;OMIM:253200	PCS		38/38			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0011410	PMID:15324318	PCS		16/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0011463	PMID:15324318	PCS		9/25			C	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0034861	OMIM:253200	TAS					P	HPO:probinson[2023-07-18]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002938	PMID:15324318	PCS		16/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000238	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002857	PMID:15324318	PCS		24/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002656	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000158	PMID:15324318	PCS		18/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001007	PMID:15324318	PCS		26/28			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001249	PMID:15324318	PCS		0/28			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0003521	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002751	PMID:15324318	PCS		22/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001385	PMID:15324318	PCS		15/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001387	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0005180	PMID:15324318	PCS		20/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002829	PMID:15324318	PCS		22/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0012185	PMID:15324318;OMIM:253200	PCS		15/38			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002869	OMIM:253200	IEA					P	HPO:iea[2012-05-28]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001537	PMID:15324318	PCS		26/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000007	OMIM:253200	IEA					I	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000768	PMID:15324318	PCS		22/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000884	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002788	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002866	OMIM:253200	IEA					P	HPO:iea[2012-05-28]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001653	PMID:15324318	PCS		27/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000885	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0003016	OMIM:253200	TAS					P	HPO:probinson[2012-05-26]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000023	PMID:15324318	PCS		8/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002240	PMID:15324318	PCS		10/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001072	PMID:15324318	PCS		26/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0012450	PMID:15324318	PCS		2/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0008432	OMIM:253200	TAS					P	HPO:probinson[2012-06-10]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002318	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000256	PMID:15324318	PCS		19/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001744	PMID:15324318	PCS		24/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000670	PMID:15324318	PCS		13/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0003025	OMIM:253200	TAS					P	HPO:probinson[2012-05-26]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0003300	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002092	PMID:15324318	PCS		4/28			P	HPO:probinson[2022-06-13];HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0011703	PMID:15324318	PCS		12/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002090	PMID:15324318	PCS		16/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0005280	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0002091	PMID:15324318	PCS		9/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0010535	PMID:15324318	PCS		23/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0011941	OMIM:253200	TAS					P	HPO:probinson[2012-06-10]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001718	PMID:15324318	PCS		2/28			P	HPO:probinson[2022-06-13]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0008301	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000943	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0001638	OMIM:253200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000268	OMIM:253200	IEA					P	HPO:iea[2009-02-17]
OMIM:253200	Mucopolysaccharidosis, type VI		HP:0000501	PMID:15324318	PCS		2/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-13]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002465	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002067	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001332	PMID:23435086	PCS		5/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001272	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001250	PMID:23435086	PCS		3/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002063	PMID:23435086	PCS		5/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002180	OMIM:300894	IEA					P	HPO:skoehler[2015-01-27]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0033329	PMID:23435086	PCS		1/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0012332	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0011463	PMID:23435086	PCS		5/5			C	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0000718	PMID:23435086	PCS		2/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0000739	PMID:23435086	PCS		1/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001423	PMID:23435086	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001268	PMID:23435086	PCS	HP:0011462	5/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001249	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002313	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002454	PMID:23435086	PCS		0/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002059	PMID:23435086	PCS		5/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001344	PMID:23435086	PCS		2/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0000750	PMID:23435086	PCS		5/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001300	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0000496	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0031936	PMID:23435086	PCS		3/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001263	PMID:23435086	PCS		5/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0012675	PMID:23435086	PCS		5/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0000726	PMID:23435086	PCS		5/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0002304	PMID:23435086	PCS		2/5			P	HPO:probinson[2023-03-05]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0000743	OMIM:300894	TAS					P	HPO:skoehler[2013-04-18]
OMIM:300894	Neurodegeneration with brain iron accumulation 5		HP:0001337	PMID:23435086	PCS		1/5			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-03-05]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0001650	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000343	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0010807	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000280	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0012307	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0031568	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0011463	PMID:34916232	PCS		4/4			C	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000916	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0003307	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0002857	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0008833	PMID:34916232	PCS					P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000699	PMID:34916232	PCS		1/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0003521	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0001385	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000431	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0002650	PMID:34916232	PCS		3/4		HP:0012825	P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0005121	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0100832	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000926	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0008301	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000007	PMID:34916232	PCS					I	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0001712	PMID:34916232	PCS		1/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0001659	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000787	PMID:34916232	PCS		1/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000687	PMID:34916232	PCS		2/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0000885	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:619698	Mucopolysaccharidosis, type X		HP:0004568	PMID:34916232	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0012385	PMID:30777867	PCS		12/12			P	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0003577	PMID:30777867	PCS		12/12			C	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0001762	PMID:30777867	PCS		0/12			P	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0001838	PMID:30777867	PCS		0/12			P	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0006394	PMID:30777867	PCS		7/11			P	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0001848	PMID:30777867	PCS		0/12			P	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0006077	PMID:30777867	PCS		10/11			P	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0001840	PMID:30777867	PCS		0/12			P	HPO:probinson[2022-08-27]
OMIM:620019	Arthrogryposis, distal, type 11		HP:0000006	PMID:30777867	PCS					I	HPO:probinson[2022-08-27]
OMIM:606960	Insulinoma tumor suppressor gene locus		HP:0001442	OMIM:606960	TAS					I	HPO:probinson[2013-01-09]
OMIM:606960	Insulinoma tumor suppressor gene locus		HP:0012197	OMIM:606960	TAS					P	HPO:probinson[2013-03-11]
OMIM:619840	Macrothrombocytopenia, isolated, 2, autosomal dominant		HP:0040185	PMID:34704371	PCS					P	HPO:probinson[2022-06-08]
OMIM:619840	Macrothrombocytopenia, isolated, 2, autosomal dominant		HP:0000006	PMID:34704371	PCS					I	HPO:probinson[2022-06-08]
OMIM:125460	Deoxyribose-5-Phosphate aldolase deficiency		HP:0001419	OMIM:125460	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:125460	Deoxyribose-5-Phosphate aldolase deficiency		HP:0000007	OMIM:125460	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:125460	Deoxyribose-5-Phosphate aldolase deficiency		HP:0012379	OMIM:125460	IEA					P	HPO:iea[2009-02-17]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0003676	PMID:15452312	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0002166	PMID:15452312	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0001300	OMIM:604187	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0002650	PMID:15452312	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0003487	PMID:15452312	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0001761	PMID:15452312	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0000012	PMID:15452312	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0003484	PMID:15452312	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0000020	OMIM:604187	IEA					P	HPO:iea[2009-02-17]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0001251	OMIM:604187	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0003593	PMID:15452312	PCS		4/4			C	HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0002064	PMID:15452312	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0002061	OMIM:604187	IEA					P	HPO:iea[2009-02-17]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0011449	OMIM:604187	TAS					P	HPO:probinson[2012-04-17]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0011448	OMIM:604187	TAS					P	HPO:probinson[2012-04-17]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0007340	PMID:15452312	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0002839	OMIM:604187	IEA					P	HPO:iea[2009-02-17]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0002936	PMID:15452312	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0006895	PMID:15452312	PCS		8/8			P	HPO:probinson[2023-02-10]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0001258	OMIM:604187	IEA					P	HPO:skoehler[2015-01-21]
OMIM:604187	Spastic paraplegia 10, autosomal dominant		HP:0000006	PMID:12355402	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001297	OMIM:249270	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001696	OMIM:249270	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0003355	OMIM:249270	IEA					P	HPO:iea[2009-02-17]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0004322	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001250	OMIM:249270	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0004860	PMID:19643445	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001251	OMIM:249270	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0002020	OMIM:249270	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0011675	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000819	PMID:19643445	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000639	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001629	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0011463	PMID:19643445	PCS		3/7			C	HPO:probinson[2022-03-25]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001609	OMIM:249270	IEA					P	HPO:iea[2009-02-17]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0011462	PMID:19643445	PCS		1/7			C	HPO:probinson[2022-03-25]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001924	OMIM:249270	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000951	OMIM:249270	IEA					P	HPO:iea[2009-02-17]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000572	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0003621	PMID:19643445	PCS		3/7			C	HPO:probinson[2022-03-25]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001263	OMIM:249270	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000407	PMID:19643445	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000007	PMID:10391221	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000546	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001638	OMIM:249270	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000648	OMIM:249270	IEA					P	HPO:skoehler[2010-06-20]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000548	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001631	OMIM:249270	TAS					P	HPO:skoehler[2012-11-18]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0001873	OMIM:249270	TAS					P	HPO:skoehler[2012-10-17]
OMIM:249270	Thiamine-Responsive megaloblastic anemia syndrome		HP:0000028	OMIM:249270	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:603830	Long QT syndrome 3		HP:0003621	PMID:11410597	PCS		3/5			C	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0001663	OMIM:603830	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603830	Long QT syndrome 3		HP:0003581	PMID:11410597	PCS		1/5			C	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0001790	PMID:15184283	PCS		1/1			P	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0005184	PMID:11410597;PMID:15184283	PCS		4/4			P	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0011841	PMID:15184283	PCS		1/1			P	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0011463	PMID:11410597	PCS		1/5			C	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0034198	PMID:15184283	PCS		1/1			C	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0001789	PMID:15184283	PCS		1/1			P	HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0001279	OMIM:603830	IEA					P	HPO:iea[2009-02-17]
OMIM:603830	Long QT syndrome 3		HP:0001664	OMIM:603830;PMID:15184283	PCS		11/11			P	HPO:probinson[2022-07-09];HPO:iea[2009-02-17]
OMIM:603830	Long QT syndrome 3		HP:0000006	PMID:11410597	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0001645	PMID:11410597	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:603830	Long QT syndrome 3		HP:0004756	PMID:15184283	PCS		1/1			P	HPO:probinson[2022-07-09]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0002751	PMID:26183434	PCS		2/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0003621	PMID:26183434	PCS		1/3			C	HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0000211	OMIM:616583	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0001387	PMID:26183434	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0002673	PMID:26183434	PCS		2/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0004322	PMID:26183434	PCS		2/3			P	HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0025258	PMID:26183434	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0034372	PMID:26183434	PCS		1/3			P	HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0002829	PMID:26183434	PCS		3/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0000946	PMID:26183434	PCS		1/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0011463	PMID:26183434	PCS		2/3			C	HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0000926	PMID:26183434	PCS		3/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0008422	PMID:26183434	PCS		2/3			P	HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0002515	PMID:26183434	PCS		3/3			P	HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0000006	PMID:26183434	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-10]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0004568	OMIM:616583	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616583	Spondyloepiphyseal dysplasia, Stanescu type		HP:0002655	PMID:26183434	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-10]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0031956	PMID:27532546	PCS		5/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0003124	PMID:27532546	PCS		1/4			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0004322	PMID:27532546	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0003573	PMID:27532546	PCS		5/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0003593	PMID:27532546	PCS		3/5			C	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0002240	PMID:27532546	PCS		4/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0003073	PMID:27532546	PCS		2/4			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0030948	PMID:27532546	PCS		0/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0012202	PMID:27532546	PCS		4/4			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0031964	PMID:27532546	PCS		4/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0011985	PMID:27532546	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0002908	PMID:27532546	PCS		4/4			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0006580	PMID:27532546	PCS		2/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0001508	PMID:27532546	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0011463	PMID:27532546	PCS		2/5			C	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0000007	PMID:27532546	PCS					I	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0000989	PMID:27532546	PCS		3/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0001744	PMID:27532546	PCS		1/5			P	HPO:probinson[2022-07-16]
OMIM:619868	Cholestasis, progressive familial intrahepatic, 10		HP:0000952	PMID:27532546	PCS		4/5			P	HPO:probinson[2022-07-16]
OMIM:252650	Mucolipidosis IV		HP:0002344	OMIM:252650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252650	Mucolipidosis IV		HP:0006989	PMID:21763169	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0007759	OMIM:252650	PCS					P	HPO:probinson[2012-04-03]
OMIM:252650	Mucolipidosis IV		HP:0007957	PMID:21763169	PCS					P	HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0004345	OMIM:252650	PCS					P	HPO:probinson[2012-04-03]
OMIM:252650	Mucolipidosis IV		HP:0000486	PMID:21763169	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0001332	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0001272	PMID:21763169	PCS					P	HPO:probinson[2012-04-03];HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0001252	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0003593	OMIM:252650	PCS					C	HPO:probinson[2012-04-03]
OMIM:252650	Mucolipidosis IV		HP:0001290	OMIM:252650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:252650	Mucolipidosis IV		HP:0011020	OMIM:252650	PCS					P	HPO:probinson[2012-04-03]
OMIM:252650	Mucolipidosis IV		HP:0007281	OMIM:252650	PCS					P	HPO:probinson[2012-04-03]
OMIM:252650	Mucolipidosis IV		HP:0007266	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0000613	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0001249	PMID:21763169	PCS					P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0000654	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0001347	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0500167	PMID:21763169	PCS					P	HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0000252	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0002510	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0001344	OMIM:252650	PCS					P	HPO:probinson[2012-04-03]
OMIM:252650	Mucolipidosis IV		HP:0003487	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0001263	PMID:21763169	PCS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0032448	OMIM:252650	IEA					P	HPO:skoehler[2019-04-18]
OMIM:252650	Mucolipidosis IV		HP:0001438	OMIM:252650	IEA					P	HPO:iea[2009-02-17]
OMIM:252650	Mucolipidosis IV		HP:0000007	PMID:10973263	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0000546	PMID:11786056	PCS	HP:0003593			HP:0003676	P	HP:probinson[2018-05-07]
OMIM:252650	Mucolipidosis IV		HP:0000648	PMID:21763169	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:252650	Mucolipidosis IV		HP:0000505	PMID:21763169	PCS					P	HP:probinson[2019-03-01]
OMIM:601941	Diabetes mellitus, insulin-dependent, 6		HP:0000819	OMIM:601941	IEA					P	HPO:iea[2009-02-17]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0000132	PMID:30171045	PCS		5/5	FEMALE		P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0005513	PMID:29941673;PMID:30171045	PCS		3/5			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0003202	PMID:30171045	PCS		0/9			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0003577	PMID:34788986	PCS		2/2			C	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0034016	PMID:29941673	PCS		0/2			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0011877	PMID:29941673;PMID:30171045;PMID:38237079	PCS		12/12			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:4000170	PMID:29941673	PCS		0/2			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0011463	PMID:38237079	PCS		1/1			C	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0000007	PMID:30171045	PCS					I	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0000978	PMID:30171045	PCS		9/9			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0000967	PMID:34788986	PCS		2/2			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0004406	PMID:38237079	PCS		1/1			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0000421	PMID:34788986;PMID:30171045	PCS		6/11			P	HPO:probinson[2024-07-01]
OMIM:620757	Thrombocytopenia 12 with or without myopathy		HP:0001873	PMID:29941673;PMID:34788986;PMID:30171045;PMID:38237079	PCS		14/14			P	HPO:probinson[2024-07-01];HPO:probinson[2024-07-01];HPO:probinson[2024-07-01]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0033605	PMID:25029335	PCS		6/6			P	HPO:probinson[2021-02-13]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001894	PMID:25029335	PCS		4/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003493	PMID:25029335;PMID:25401470	PCS		6/10			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0200039	PMID:25029335	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0025300	PMID:25401470	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003593	PMID:25029335	PCS		2/6			C	HPO:probinson[2022-06-03]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0010783	PMID:25029335	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0033425	PMID:25029335	PCS		3/3			P	HPO:probinson[2021-02-13]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0008070	PMID:25401470	PCS		3/4			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0033505	PMID:25029335	PCS		6/6			P	HPO:probinson[2022-06-03]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0033250	PMID:25029335	PCS		3/3			P	HPO:probinson[2020-12-07]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001508	PMID:25029335;PMID:25401470	PCS		10/10			P	HPO:probinson[2020-10-26];HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0002719	PMID:25029335	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001903	PMID:25029335	PCS		2/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001009	PMID:25029335	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001888	PMID:25029335	PCS		5/5			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003623	PMID:25029335	PCS		4/6			C	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-26];HPO:probinson[2022-06-03]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003565	PMID:25029335;PMID:25401470	PCS		9/9			P	HPO:probinson[2020-10-26];HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003202	PMID:25029335	PCS		2/6			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001387	PMID:25029335	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001882	PMID:25029335	PCS		5/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0030880	PMID:25029335	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003261	PMID:25029335	PCS		5/5			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0033434	PMID:25029335	PCS		4/6			P	HPO:probinson[2021-02-13]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0011227	PMID:25029335;PMID:25401470	PCS		9/9			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0002829	PMID:25029335	PCS		2/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0032230	PMID:25029335	PCS		1/6			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0100614	PMID:25029335	PCS		2/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0002729	PMID:25401470	PCS		3/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0000965	PMID:25029335	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0001954	PMID:25401470	PCS		3/4			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0000988	PMID:25029335	PCS					P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0002923	PMID:25401470	PCS		4/4			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003613	PMID:25029335	PCS		5/6			P	HPO:probinson[2020-10-26];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0008404	PMID:25029335	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0002205	PMID:25029335	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0002206	PMID:25029335;PMID:25401470	PCS		6/10			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0002789	PMID:25029335	PCS		2/6			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0000006	PMID:25029335	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0003237	PMID:25029335	PCS		5/5			P	HPO:probinson[2020-10-26]
OMIM:615934	STING-associated vasculopathy, infantile-onset		HP:0033280	PMID:25029335	PCS		6/6			P	HPO:probinson[2020-12-07]
OMIM:612097	Deafness, unilateral, with delayed endolymphatic hydrops		HP:0000969	OMIM:612097	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612097	Deafness, unilateral, with delayed endolymphatic hydrops		HP:0009900	OMIM:612097	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612097	Deafness, unilateral, with delayed endolymphatic hydrops		HP:0000006	OMIM:612097	IEA					I	HPO:skoehler[2010-06-19]
OMIM:161550	Nasopharyngeal carcinoma		HP:0002664	OMIM:161550	IEA					P	HPO:iea[2009-02-17]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0005403	PMID:10899029;PMID:11023514	PCS		11/11			P	HPO:probinson[2022-08-14];HPO:probinson[2017-08-12];HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0002014	OMIM:608971	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0000155	PMID:11023514	PCS					P	HPO:probinson[2017-08-12]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0004430	PMID:11023514	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0003593	PMID:10899029	PCS		1/1			C	HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0002240	OMIM:608971	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0002020	PMID:10899029	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0002090	OMIM:608971	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0005390	OMIM:608971	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0002728	PMID:10899029	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0000403	PMID:10899029	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0002716	OMIM:608971	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0000964	OMIM:608971	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0000007	PMID:11023514	PCS					I	HPO:skoehler[2012-10-17]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0008866	PMID:11023514	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0000388	OMIM:608971	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608971	Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive		HP:0001744	OMIM:608971	TAS					P	HPO:skoehler[2012-10-17]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0002089	PMID:33565183	PCS		3/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0030674	PMID:33565183	PCS		3/3			C	HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0002240	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0002719	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0001629	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0002616	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000414	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000878	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000256	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0031834	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000494	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0001561	PMID:33565183	PCS		2/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0001762	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0004971	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000331	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0004691	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0002092	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0011604	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000609	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0009110	PMID:33565183	PCS		2/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0009112	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000007	PMID:33565183	PCS					I	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0006101	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0003417	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0004209	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000465	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000028	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000369	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0000347	PMID:33565183	PCS		2/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620025	Diaphragmatic hernia 4, with cardiovascular defects		HP:0002643	PMID:33565183	PCS		1/3			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:614380	Complement component 4A deficiency		HP:0000099	OMIM:614380	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614380	Complement component 4A deficiency		HP:0000992	OMIM:614380	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614380	Complement component 4A deficiency		HP:0025434	OMIM:614380	TAS					P	HPO:probinson[2021-09-06]
OMIM:614380	Complement component 4A deficiency		HP:0000979	OMIM:614380	TAS					P	HPO:skoehler[2016-03-31]
OMIM:614380	Complement component 4A deficiency		HP:0000007	OMIM:614380	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614380	Complement component 4A deficiency		HP:0002725	OMIM:614380	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614380	Complement component 4A deficiency		HP:0045042	OMIM:614380	TAS					P	HPO:probinson[2021-09-06]
OMIM:614380	Complement component 4A deficiency		HP:0002633	OMIM:614380	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000486	PMID:24614104	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000343	OMIM:615075	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000540	PMID:24614104	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001252	PMID:24614104	PCS		3/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0003593	PMID:24614104	PCS		1/4			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0033128	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000718	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000711	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000219	PMID:24614104	PCS		1/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000218	OMIM:615075	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0025336	PMID:24614104	PCS		3/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001500	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000455	PMID:24614104	PCS		4/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001249	PMID:24614104	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0003623	PMID:24614104	PCS		3/4			C	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001264	PMID:24614104	PCS		1/4		HP:0003676	P	HPO:skoehler[2014-07-11];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0002015	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0002650	PMID:24614104	PCS		2/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0002079	OMIM:615075	TAS		1/1			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0031936	PMID:24614104	PCS		2/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0011968	PMID:24614104	PCS		2/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001263	PMID:24614104	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0002191	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001518	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0011451	PMID:24614104	PCS		4/4			P	HPO:probinson[2022-07-08];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000729	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000648	OMIM:615075	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0030490	OMIM:615075	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001257	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0001510	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000006	PMID:23033978	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-08]
OMIM:615075	Neurodevelopmental disorder with spastic diplegia and visual defects		HP:0000742	PMID:24614104	PCS		1/4			P	HPO:probinson[2022-07-08]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000121	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000340	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0003355	PMID:31479177	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001252	OMIM:613404	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0002240	PMID:31479177	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0003076	PMID:31479177	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001290	OMIM:613404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0200084	OMIM:613404	TAS					P	HPO:skoehler[2013-06-04]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001508	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001629	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001947	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001522	PMID:31479177	PCS		1/1			C	HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0002910	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001884	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000952	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001942	PMID:31479177	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001667	OMIM:613404	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0002611	PMID:31479177	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0003623	PMID:31479177	PCS		1/1			C	HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001385	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000252	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000112	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0009806	OMIM:613404	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001263	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000093	PMID:31479177	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0002908	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0008064	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0001339	OMIM:613404	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0002804	PMID:31479177	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000007	PMID:20190753	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000989	PMID:31479177	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:613404	Arthrogryposis, renal dysfunction, and cholestasis 2		HP:0000369	OMIM:613404	TAS					P	HPO:skoehler[2012-10-17]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0002751	PMID:28475863	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000365	PMID:28475863	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000541	PMID:28475863	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0001762	PMID:28475863	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0004322	PMID:28475863	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000023	PMID:28475863	PCS		1/5			P	HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0001382	PMID:28475863	PCS		5/5			P	HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0011003	PMID:28475863	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0012095	PMID:28475863	PCS		2/5			P	HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0001537	PMID:28475863	PCS		1/5			P	HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000007	PMID:28475863	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000612	PMID:28475863	PCS	HP:0003577	2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0002947	PMID:28475863	PCS		1/5			P	HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000768	PMID:28475863	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000567	PMID:28475863	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0000501	PMID:28475863	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-19]
OMIM:617662	Joint laxity, short stature, and myopia		HP:0001249	PMID:28475863	PCS		0/5			P	HPO:probinson[2023-01-19]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0001342	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0031318	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0003577	PMID:34888509;PMID:31517052	PCS		3/3			C	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0030149	PMID:34888509	PCS		1/2			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0004751	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0011712	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0011701	PMID:34888509	PCS		1/2			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0031333	PMID:34888509	PCS		1/2			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0031676	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0033008	PMID:34888509;PMID:31517052	PCS		2/3			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0012666	PMID:34888509;PMID:31517052	PCS		3/3			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0005180	PMID:34888509	PCS		1/2			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0031295	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0000007	PMID:31517052	PCS					I	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0001649	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0001659	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0003811	PMID:34888509	PCS		2/2			C	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0001653	PMID:31517052	PCS		1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0001644	PMID:31517052	PCS	HP:0003577	1/1			P	HPO:probinson[2022-06-26]
OMIM:619897	Cardiomyopathy, dilated, 2G		HP:0001644	PMID:34888509	PCS		2/2			P	HPO:probinson[2022-06-26]
OMIM:300843	Bornholm eye disease		HP:0007703	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0000483	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0000609	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0001419	OMIM:300843	TAS					I	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0000646	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0011522	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0011521	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0011003	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300843	Bornholm eye disease		HP:0000654	OMIM:300843	TAS					P	HPO:skoehler[2012-10-14]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0003477	OMIM:607317	IEA					P	HPO:iea[2009-02-17]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0000640	PMID:29604224	PCS		1/12			P	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001332	OMIM:607317	IEA					P	HPO:skoehler[2019-02-22]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0003693	OMIM:607317	IEA					P	HPO:skoehler[2019-02-22]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001250	PMID:29604224	PCS		1/12			P	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001272	PMID:29604224	PCS		7/12			P	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0002066	PMID:29604224	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001251	PMID:29604224	PCS		10/12			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0002460	OMIM:607317	IEA					P	HPO:skoehler[2019-02-22]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0003593	PMID:29604224	PCS		2/12			C	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0002380	OMIM:607317	IEA					P	HPO:iea[2009-02-17]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001270	PMID:29604224	PCS		3/12			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0033051	PMID:29604224	PCS		1/12			P	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0011463	PMID:29604224	PCS		2/12			C	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0007340	PMID:29604224	PCS		6/11			P	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0011462	PMID:29604224	PCS		8/12			C	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0002359	OMIM:607317	IEA					P	HPO:skoehler[2019-02-22]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001347	PMID:29604224	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0008936	OMIM:607317	IEA					P	HPO:skoehler[2019-02-22]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0000473	PMID:29604224	PCS		1/12			P	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0000252	OMIM:607317	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0003487	OMIM:607317	IEA					P	HPO:iea[2009-02-17]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001761	OMIM:607317	IEA					P	HPO:iea[2009-02-17]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001260	PMID:29604224	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0032105	PMID:29604224	PCS		3/12			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0000007	PMID:29604224	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0007256	PMID:29604224	PCS		10/12			P	HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001257	PMID:29604224	PCS		3/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0002500	OMIM:607317	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0007338	PMID:29604224	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-19]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001337	OMIM:607317	IEA					P	HPO:skoehler[2019-02-22]
OMIM:607317	Spinocerebellar ataxia, autosomal recessive 4		HP:0001336	PMID:29604224	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001298	PMID:18179882	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0002069	PMID:18179882	PCS		2/5			P	HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0003577	PMID:18179882	PCS		9/9			C	HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0000365	OMIM:618237	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001332	PMID:18179882	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001371	OMIM:618237	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0003198	OMIM:618237	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001272	PMID:18179882	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001290	PMID:18179882	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001508	PMID:18179882	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0000639	PMID:18179882	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0000737	PMID:18179882	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0000817	PMID:18179882	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001942	PMID:18179882	PCS	HP:0003577	9/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0007305	PMID:18179882	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001347	PMID:18179882	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0002510	PMID:18179882	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0002151	PMID:18179882	PCS		9/9			P	HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0011923	PMID:18179882	PCS		4/4			P	HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001639	PMID:18179882	PCS	HP:0011463	1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0002808	PMID:18179882	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0000007	PMID:18179882	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0000648	PMID:18179882	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-26]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0001511	OMIM:618237	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618237	Mitochondrial complex I deficiency, nuclear type 15		HP:0003811	PMID:18179882	PCS		3/9			C	HPO:probinson[2022-05-26]
OMIM:275210	Restrictive dermopathy 1		HP:0000561	OMIM:275210	IEA					P	HPO:skoehler[2018-10-08]
OMIM:275210	Restrictive dermopathy 1		HP:0001371	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000160	PMID:15317753	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0005253	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0012745	OMIM:275210	TAS					P	HPO:skoehler[2014-03-24]
OMIM:275210	Restrictive dermopathy 1		HP:0045075	PMID:15317753	PCS		7/7			P	HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0011414	OMIM:275210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:275210	Restrictive dermopathy 1		HP:0100840	OMIM:275210	TAS					P	HPO:skoehler[2013-06-05]
OMIM:275210	Restrictive dermopathy 1		HP:0006391	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0011461	PMID:15317753	PCS		7/7			C	HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0000316	PMID:15317753	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0000239	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0003826	OMIM:275210	IEA					C	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000835	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0001643	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0002751	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000176	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000453	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000695	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0003121	PMID:19504603	PCS		1/1			P	HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0034197	PMID:19504603	PCS		1/1			C	HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0007394	PMID:15317753	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0040189	PMID:19504603	PCS		1/1			P	HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0000007	PMID:15317753	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0006585	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000444	PMID:15317753	PCS		7/7			P	HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0000047	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000369	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000963	PMID:19504603	PCS		1/1			P	HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0000962	OMIM:275210	TAS					P	HPO:probinson[2024-12-03]
OMIM:275210	Restrictive dermopathy 1		HP:0003577	PMID:15317753	PCS		7/7			C	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:275210	Restrictive dermopathy 1		HP:0002089	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0009839	PMID:15317753	PCS		5/5			P	HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0000260	PMID:15317753	PCS		7/7			P	HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0000581	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0005474	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0001196	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000418	OMIM:275210	IEA					P	HPO:skoehler[2010-06-20]
OMIM:275210	Restrictive dermopathy 1		HP:0025712	PMID:19504603	PCS		1/1			P	HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0000653	PMID:15317753	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0000894	PMID:15317753	PCS		7/7			P	HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0001788	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0001622	PMID:15317753;PMID:19504603	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0200041	PMID:15317753	PCS		7/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0001562	PMID:19504603	PCS	HP:0011461	1/1			P	HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0001561	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000073	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0031013	PMID:15317753	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0005280	PMID:19504603	PCS		1/1			P	HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0012478	OMIM:275210	IEA					P	HPO:skoehler[2019-02-22]
OMIM:275210	Restrictive dermopathy 1		HP:0001838	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0001558	PMID:15317753;PMID:19504603	PCS	HP:0011461	8/8			P	HPO:probinson[2022-05-29];HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0001511	PMID:15317753	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0003811	PMID:15317753;PMID:19504603	PCS		8/8			C	HPO:probinson[2022-05-29];HPO:probinson[2022-08-22]
OMIM:275210	Restrictive dermopathy 1		HP:0001631	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0000347	PMID:15317753	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:275210	Restrictive dermopathy 1		HP:0001799	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:275210	Restrictive dermopathy 1		HP:0006645	OMIM:275210	TAS					P	HPO:probinson[2012-05-28]
OMIM:275210	Restrictive dermopathy 1		HP:0000621	OMIM:275210	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000561	PMID:24108658	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:0003577	PMID:25790162;PMID:24108658;PMID:15214011	PCS		14/14			C	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2022-03-31]
OMIM:154500	Treacher Collins syndrome 1		HP:0000384	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000486	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0004443	PMID:24108658;PMID:15214011	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:0000160	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000185	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0004440	PMID:24108658;PMID:15214011	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:6000612	PMID:24108658;PMID:15214011	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:0008551	PMID:25790162	PCS		51/72			P	HPO:iea[2018-03-13]
OMIM:154500	Treacher Collins syndrome 1		HP:0000238	PMID:24108658;PMID:15214011	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:0001627	PMID:19050407	PCS					P	HPO:lccarmody[2018-10-18]
OMIM:154500	Treacher Collins syndrome 1		HP:0000636	PMID:25790162	PCS		43/66			P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000377	PMID:24108658;PMID:15214011	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:0000652	PMID:24108658;PMID:15214011	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2009-02-17];HPO:probinson[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:0000413	PMID:25790162;PMID:24108658;PMID:15214011	PCS		48/65			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2018-03-13]
OMIM:154500	Treacher Collins syndrome 1		HP:0001249	PMID:25790162	PCS		1/53			P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000572	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000154	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000197	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000175	PMID:25790162;PMID:24108658;PMID:15214011	PCS		17/68			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:skoehler[2012-10-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000494	PMID:25790162;PMID:24108658;PMID:15214011	PCS		74/74			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:154500	Treacher Collins syndrome 1		HP:0000453	PMID:25790162;PMID:24108658;PMID:15214011	PCS		9/60			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000272	PMID:25790162;PMID:24108658;PMID:15214011	PCS		74/75			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000508	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0009555	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0009554	PMID:25790162;PMID:24108658	PCS		24/49			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000405	PMID:25790162;PMID:24108658	PCS		66/73			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0007633	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0007776	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0007678	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000006	PMID:25790162	PCS					I	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000028	OMIM:154500	IEA					P	HPO:iea[2009-02-17]
OMIM:154500	Treacher Collins syndrome 1		HP:0000347	PMID:25790162	PCS	HP:0003577	62/71			P	HPO:iea[2018-03-13]
OMIM:154500	Treacher Collins syndrome 1		HP:0000347	PMID:24108658	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:154500	Treacher Collins syndrome 1		HP:0000347	PMID:15214011	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:603165	Dermatitis, atopic		HP:0000563	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0001047	OMIM:603165	TAS					P	HPO:skoehler[2015-01-21]
OMIM:603165	Dermatitis, atopic		HP:0000980	OMIM:603165	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603165	Dermatitis, atopic		HP:0001041	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0002099	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0001581	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0012537	OMIM:603165	TAS					P	HPO:skoehler[2014-01-28]
OMIM:603165	Dermatitis, atopic		HP:0003193	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0008064	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0000518	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0000958	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0032152	OMIM:603165	IEA					P	HPO:skoehler[2019-02-22]
OMIM:603165	Dermatitis, atopic		HP:0011232	OMIM:603165	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603165	Dermatitis, atopic		HP:0000509	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0001939	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0007453	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0000964	OMIM:603165	IEA					P	HPO:iea[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0000989	OMIM:603165	TAS					P	HPO:skoehler[2009-02-17]
OMIM:603165	Dermatitis, atopic		HP:0000006	OMIM:603165	IEA					I	HPO:iea[2009-02-17]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0003445	PMID:20142617	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0030237	PMID:20142617	PCS		2/2			P	HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0003376	PMID:20142617	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0001288	PMID:20142617	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0008959	PMID:20142617	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0003388	PMID:20142617	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0009053	PMID:20142617	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0011462	PMID:20142617	PCS		2/2			C	HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0009830	PMID:20142617	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0007149	PMID:20142617	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0008954	PMID:20142617	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0003438	PMID:20142617	PCS		2/2			P	HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0000006	PMID:20142617	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0003677	PMID:20142617	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0006844	PMID:20142617	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:613376	Neuronopathy, distal hereditary motor, type IIC		HP:0008944	PMID:20142617	PCS		1/2			P	HPO:probinson[2022-10-01]
OMIM:615707	Immunodeficiency 20		HP:0020086	PMID:8874200	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0003593	PMID:8608639	PCS		1/1			C	HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0030828	PMID:8874200	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0011108	PMID:8608639	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0032170	PMID:8874200	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0012177	PMID:8608639	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0033166	PMID:8874200	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0000403	PMID:8608639	PCS		1/1			P	HPO:skoehler[2014-05-04];HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0000007	PMID:8608639	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0002205	OMIM:615707	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615707	Immunodeficiency 20		HP:0410028	PMID:8608639	PCS		1/1			P	HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0002721	PMID:8608639	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2021-05-30]
OMIM:615707	Immunodeficiency 20		HP:0040218	PMID:8608639;PMID:8874200	PCS		1/2			P	HPO:probinson[2021-05-30];HPO:probinson[2021-05-30];HPO:probinson[2021-05-30]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0000992	OMIM:278720	TAS					P	HPO:probinson[2009-02-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0003079	OMIM:278720	IEA					P	HPO:probinson[2009-02-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0004334	PMID:14662655	PCS		2/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0000491	OMIM:278720	IEA					P	HPO:probinson[2009-02-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0006739	PMID:14662655	PCS		3/4			P	HPO:probinson[2012-08-01];HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0002671	PMID:14662655	PCS		2/4			P	HPO:probinson[2012-08-01];HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0001480	PMID:14662655	PCS		2/4			P	HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0001010	OMIM:278720	TAS					P	HPO:skoehler[2012-10-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0012056	PMID:14662655	PCS		2/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0011463	PMID:14662655	PCS		4/4			C	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0000509	OMIM:278720	IEA					P	HPO:probinson[2009-02-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0000613	OMIM:278720	TAS					P	HPO:probinson[2009-02-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0001009	PMID:14662655	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0000007	PMID:8298653	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0000656	OMIM:278720	IEA					P	HPO:probinson[2009-02-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0025127	PMID:14662655	PCS		2/2			P	HPO:probinson[2023-02-04]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0001029	OMIM:278720	IEA					P	HPO:probinson[2009-02-17]
OMIM:278720	Xeroderma pigmentosum, group C		HP:0000621	OMIM:278720	IEA					P	HPO:probinson[2009-02-17]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0000044	PMID:9371856	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0000054	PMID:9371856	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0003621	PMID:9371856	PCS		2/2			C	HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0000771	PMID:9371856	PCS		0/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0000789	OMIM:146110	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0000007	PMID:9371856	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0004408	PMID:9371856	PCS		0/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0008734	PMID:9371856	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0000028	OMIM:146110	TAS					P	HPO:skoehler[2015-04-05]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0002225	PMID:9371856	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0000786	PMID:9371856	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:146110	Hypogonadotropic hypogonadism 7 without anosmia		HP:0002215	PMID:9371856	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:611561	Meckel syndrome, type 5		HP:0000175	PMID:17558409	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0002323	PMID:17558409	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0003577	PMID:17558409	PCS		3/3			C	HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0001162	PMID:17558409	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0001408	PMID:17558409	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0002085	PMID:17558409	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0000107	PMID:17558409	PCS		3/3			P	HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0000007	PMID:17558409	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0000568	PMID:17558409	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0006487	OMIM:611561	TAS		2/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0001830	PMID:17558409	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:611561	Meckel syndrome, type 5		HP:0000204	PMID:17558409	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608030	Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia		HP:0001265	OMIM:608030	TAS					P	HPO:probinson[2013-03-24]
OMIM:608030	Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia		HP:0001288	PMID:20668259	PCS					P	HPO:probinson[2013-03-24]
OMIM:608030	Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia		HP:0002380	OMIM:608030	TAS					P	HPO:probinson[2013-03-24]
OMIM:608030	Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia		HP:0007354	OMIM:608030	TAS					P	HPO:skoehler[2015-01-19]
OMIM:608030	Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia		HP:0002529	OMIM:608030	TAS					P	HPO:probinson[2013-03-24]
OMIM:608030	Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia		HP:0007126	OMIM:608030	TAS					P	HPO:probinson[2013-03-24]
OMIM:608030	Amyotrophic lateral sclerosis 6, with or without frontotemporal dementia		HP:0000006	PMID:20668259	PCS					I	HPO:probinson[2013-01-09]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000286	PMID:29726930	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0005359	PMID:29726930	PCS		1/4			P	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0003577	PMID:29726930	PCS		4/4			C	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000189	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0004322	PMID:29726930	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0009918	PMID:29726930	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0001076	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0410030	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0011342	PMID:29726930	PCS		1/4			P	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0002937	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000437	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000316	PMID:29726930	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000912	PMID:29726930	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000455	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000378	PMID:29726930	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0001643	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000872	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0001642	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000396	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0005403	PMID:29726930	PCS		1/4			P	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000175	PMID:29726930	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0002650	PMID:29726930	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000294	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000470	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0005280	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000829	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0009471	PMID:29726930	PCS		3/4			P	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0009276	PMID:29726930	PCS		3/4			P	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0002808	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000729	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0001719	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000824	PMID:29726930	PCS		1/4			P	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0002846	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0001631	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000465	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0007018	PMID:29726930	PCS		1/4			P	HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000006	PMID:29726930	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000248	PMID:29726930	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000369	PMID:29726930	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:618223	Vertebral anomalies and variable endocrine and T-cell dysfunction		HP:0000325	PMID:29726930	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-23]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0002015	PMID:21857683	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0003676	PMID:21857683	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0003621	PMID:21857683	PCS		1/35			C	HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0003596	PMID:21857683	PCS		16/35			C	HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0002145	OMIM:300857	IEA		7/40			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0001332	OMIM:300857	TAS					P	HPO:skoehler[2014-11-26]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0001260	PMID:21857683	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0003584	PMID:21857683	PCS		3/35			C	HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0003581	OMIM:300857	IEA					C	HPO:skoehler[2013-01-11]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0002171	OMIM:300857	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0003470	OMIM:300857	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0011462	PMID:21857683	PCS		15/35			C	HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0007354	PMID:21857683	PCS		34/40			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0001423	PMID:21857683	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-27]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0002305	OMIM:300857	TAS					P	HPO:skoehler[2014-11-26]
OMIM:300857	Amyotrophic lateral sclerosis 15 with or without frontotemporal dementia		HP:0003447	OMIM:300857	IEA					P	HPO:skoehler[2018-10-08]
OMIM:263300	Polycythemia vera		HP:0001342	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0005513	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0001894	PMID:15793561	PCS		14/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0003596	PMID:15793561	PCS		17/31			C	HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0001442	PMID:15793561	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0003584	PMID:15793561	PCS		13/31			C	HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0001907	OMIM:263300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:263300	Polycythemia vera		HP:0025709	PMID:15793561	PCS		1/31			C	HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0001900	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0001977	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0001899	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0002639	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0002637	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0003745	OMIM:263300	IEA					I	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0001873	PMID:15793561	PCS		0/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0002239	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0000006	OMIM:263300	IEA					I	HPO:iea[2009-02-17]
OMIM:263300	Polycythemia vera		HP:0001744	PMID:15793561	PCS		30/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0001898	PMID:15793561	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:263300	Polycythemia vera		HP:0001974	OMIM:263300	IEA					P	HPO:iea[2009-02-17]
OMIM:147540	Insect stings, hypersensitivity to		HP:0000006	OMIM:147540	IEA					I	HPO:iea[2009-02-17]
OMIM:147540	Insect stings, hypersensitivity to		HP:0000951	OMIM:147540	IEA					P	HPO:iea[2009-02-17]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003236	PMID:16685652	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0010628	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003676	OMIM:610131	IEA					C	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001272	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001250	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001392	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001252	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0002020	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001290	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003690	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0011675	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0011713	PMID:16685652	PCS		1/1			P	HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001508	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0100704	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0025710	PMID:16685652	PCS		1/1			C	HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0002019	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0002910	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003688	PMID:16685652	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003546	PMID:16685652	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0002578	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003689	PMID:16685652	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003326	PMID:16685652	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003323	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0000590	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0003581	OMIM:610131	IEA					C	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001263	OMIM:610131	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0002151	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0040270	PMID:16685652	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0034306	PMID:16685652	PCS		1/1		HP:0025303	P	HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0000508	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0000006	PMID:16685652	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-18]
OMIM:610131	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4		HP:0001952	OMIM:610131	IEA					P	HPO:skoehler[2010-06-19]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0003577	OMIM:609460	TAS					C	HPO:skoehler[2015-12-30]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0002365	OMIM:609460	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000485	PMID:23427148	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000540	PMID:23427148	PCS		2/5			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0012804	OMIM:609460	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0001252	PMID:23427148	PCS		5/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0012427	PMID:23427148	PCS		1/5			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0012704	PMID:23427148	PCS		1/5			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0008070	PMID:23427148	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0001629	PMID:23427148	PCS		1/5			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0012471	OMIM:609460	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000414	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0001302	OMIM:609460	TAS					P	HPO:skoehler[2014-08-24]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0006610	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0200020	OMIM:609460	TAS					P	HPO:probinson[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0001249	PMID:23427148	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000677	PMID:23427148	PCS		1/5			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0002553	PMID:23427148	PCS					P	HPO:probinson[2012-03-02];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000494	PMID:23427148	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000252	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000076	PMID:23427148	PCS		1/4			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000574	OMIM:609460	PCS					P	HPO:probinson[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000431	PMID:23427148	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000232	PMID:23427148	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0002079	PMID:23427148	PCS		2/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000592	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0001263	PMID:23427148	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0002251	PMID:23427148;PMID:15883926	PCS		14/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000470	PMID:23427148	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0001182	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000506	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000508	PMID:23427148	PCS		2/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0002509	PMID:23427148	PCS		2/5			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000327	PMID:23427148	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000426	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000007	PMID:15883926	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0004209	PMID:23427148	PCS					P	HPO:probinson[2023-01-17];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0001659	PMID:23427148	PCS		1/5			P	HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0200055	PMID:23427148	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000664	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000322	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0000369	OMIM:609460	IEA					P	HPO:iea[2009-02-17]
OMIM:609460	Goldberg-Shprintzen syndrome		HP:0002126	PMID:23427148;PMID:15883926	PCS		6/10			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-17];HPO:probinson[2023-01-17]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0002069	PMID:25954030	PCS		2/3			P	HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0003621	PMID:25954030	PCS		1/2			C	HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0003676	PMID:25954030	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0002650	PMID:25954030	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0002133	PMID:25954030	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0002123	PMID:25954030	PCS		1/2			P	HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0002066	PMID:25954030	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0000171	PMID:25954030	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0001274	PMID:25954030	PCS		1/2			P	HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0001263	PMID:25954030	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0032327	PMID:25954030	PCS		1/2			P	HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0034360	PMID:25954030	PCS		1/2			P	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0011463	PMID:25954030	PCS		1/2			C	HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0000007	PMID:25954030	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0002119	PMID:25954030	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0002359	PMID:25954030	PCS		1/2			P	HPO:probinson[2023-03-31]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0009778	PMID:25954030	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0003700	PMID:25954030	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0001336	PMID:25954030	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616540	Epilepsy, progressive myoclonic, 9		HP:0009879	PMID:25954030	PCS		1/2			P	HPO:probinson[2023-03-31]
OMIM:619673	Spermatogenic failure 62		HP:0003251	PMID:31125047	PCS		2/2			P	HPO:probinson[2022-02-12]
OMIM:619673	Spermatogenic failure 62		HP:0000007	PMID:31125047	PCS					I	HPO:probinson[2022-02-12]
OMIM:619673	Spermatogenic failure 62		HP:0011961	PMID:31125047	PCS		2/2			P	HPO:probinson[2022-02-12]
OMIM:619673	Spermatogenic failure 62		HP:0031039	PMID:31125047	PCS		2/2			P	HPO:probinson[2022-02-12]
OMIM:602535	Marshall-Smith syndrome		HP:0004325	PMID:24924640	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001331	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001212	PMID:20949508	PCS		8/14			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0000365	PMID:20949508;PMID:20673863	PCS		13/25			P	HPO:probinson[2022-05-22];HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0004322	PMID:24924640	PCS		12/17			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002021	PMID:20949508	PCS		2/19			P	HPO:probinson[2022-05-22];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0003196	PMID:20949508;PMID:20673863	PCS		22/28			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-03-04];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0012472	PMID:20949508;PMID:20673863	PCS		18/28			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-04];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0000998	PMID:20949508;PMID:20673863	PCS		23/28			P	HPO:probinson[2022-05-22];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000238	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000879	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0002812	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0003745	OMIM:602535	IEA					I	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0001601	PMID:24924640;PMID:26200704	PCS		3/4			P	HP:probinson[2022-03-04];HPO:probinson[2022-03-04];HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0003623	PMID:24924640	PCS		2/2			C	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000995	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002553	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000098	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0011800	PMID:20949508;PMID:24924640	PCS		19/21			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-03-04];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0011003	PMID:20673863	PCS		3/9			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000767	PMID:24924640	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002307	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0004209	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002942	PMID:20673863	PCS		5/9			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002788	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002943	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000520	PMID:20949508;PMID:20673863;PMID:26200704	PCS		30/30			P	HPO:probinson[2022-05-22];HPO:probinson[2022-03-04];HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000369	PMID:20949508	PCS		10/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0000006	PMID:20673863	PCS					I	HPO:skoehler[2012-12-03];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001276	PMID:20949508	PCS		4/15			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0010307	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000463	PMID:20949508;OMIM:602535;PMID:26200704	PCS		23/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22];HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001274	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0001270	PMID:24924640	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0008070	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001822	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000337	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002119	PMID:20949508;PMID:20673863;PMID:26200704	PCS		4/25			P	HPO:probinson[2022-05-22];HPO:probinson[2022-03-04];HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002757	PMID:20949508	PCS		4/19			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0000218	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001302	PMID:20949508;OMIM:602535;PMID:20673863	PCS		12/33			P	HPO:probinson[2022-05-22];HPO:probinson[2022-03-04];HPO:skoehler[2012-10-17]
OMIM:602535	Marshall-Smith syndrome		HP:0009845	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0000212	PMID:20949508;PMID:20673863;PMID:26200704	PCS		12/28			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-03-04];HPO:probinson[2022-05-22];HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0008513	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001545	PMID:20949508	PCS		1/19			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0002650	PMID:20673863	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000750	PMID:20673863;PMID:26200704	PCS		5/6			P	HPO:probinson[2022-03-04];HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001321	PMID:24924640	PCS		1/10			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0003100	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0000592	PMID:20949508;PMID:20673863;PMID:26200704	PCS		25/30			P	HPO:probinson[2022-05-22];HPO:iea[2009-02-17];HPO:probinson[2022-03-04];HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0003184	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002092	PMID:20949508	PCS		1/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0002808	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0006682	PMID:24924640	PCS		1/17			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0009797	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000348	PMID:20949508;PMID:20673863	PCS		28/28			P	HPO:probinson[2022-05-22];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0006048	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0002645	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002007	PMID:24924640	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000586	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0000501	PMID:20949508	PCS		3/17			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0002100	PMID:24924640	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0003311	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0002341	PMID:20949508	PCS		2/19			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0001252	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0000162	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0005176	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0011220	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001643	PMID:24924640	PCS		1/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000278	PMID:20949508;PMID:20673863	PCS		25/28			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-03-04];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0001249	PMID:24924640	PCS		16/16			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002751	PMID:20949508	PCS		10/19			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0001385	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000574	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0010759	PMID:20949508;PMID:20673863	PCS		28/28			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-03-04];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0002870	PMID:20949508	PCS		9/15			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0000453	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0002079	PMID:24924640	PCS		2/10			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000452	PMID:20949508;PMID:20673863	PCS		8/27			P	HPO:probinson[2022-05-22];HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0011968	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000691	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001263	PMID:20949508;PMID:20673863;PMID:26200704	PCS		29/29			P	HPO:probinson[2022-05-22];HPO:probinson[2022-03-04];HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000609	PMID:20949508	PCS		5/16			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0001537	PMID:20949508;PMID:20673863;PMID:24924640	PCS		6/43			P	HPO:probinson[2022-05-22];HPO:iea[2009-02-17];HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001539	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0005616	PMID:24924640	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000322	PMID:20949508	PCS		13/19			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0008689	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000325	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002104	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0011951	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001629	PMID:20673863	PCS		2/9			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001508	PMID:24924640	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0040079	PMID:20949508	PCS		8/14			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0009882	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0001348	PMID:20949508	PCS		5/15			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0006536	PMID:24924640	PCS		16/17			P	HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000396	PMID:24924640	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0008936	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001363	PMID:20949508	PCS		1/19			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0002059	PMID:24924640	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0031936	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0002299	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0005280	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0003819	OMIM:602535	IEA					C	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0000308	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000822	OMIM:602535	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602535	Marshall-Smith syndrome		HP:0006642	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0000664	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0003778	OMIM:602535	IEA					P	HPO:iea[2009-02-17]
OMIM:602535	Marshall-Smith syndrome		HP:0000268	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001631	PMID:24924640	PCS		1/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0001238	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0000545	PMID:20949508	PCS		9/18			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0000028	PMID:20949508	PCS		3/8			P	HPO:probinson[2022-05-22]
OMIM:602535	Marshall-Smith syndrome		HP:0000269	PMID:26200704	PCS		1/2			P	HP:probinson[2022-03-04]
OMIM:602535	Marshall-Smith syndrome		HP:0003414	PMID:24924640	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-04]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0001561	OMIM:266250	IEA					P	HPO:iea[2009-02-17]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0003819	OMIM:266250	IEA					C	HPO:iea[2009-02-17]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0009113	OMIM:266250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0001284	OMIM:266250	IEA					P	HPO:iea[2009-02-17]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0002460	OMIM:266250	IEA					P	HPO:iea[2009-02-17]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0000007	OMIM:266250	IEA					I	HPO:iea[2009-02-17]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0001319	OMIM:266250	IEA					P	HPO:iea[2009-02-17]
OMIM:266250	Radiculoneuropathy, fatal neonatal		HP:0002028	OMIM:266250	IEA					P	HPO:iea[2009-02-17]
OMIM:614431	Ventricular septal defect 2		HP:0003577	PMID:16287139	PCS		1/1			C	HPO:probinson[2023-01-30]
OMIM:614431	Ventricular septal defect 2		HP:0011682	PMID:16287139	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-01-30]
OMIM:614431	Ventricular septal defect 2		HP:0000006	PMID:16287139	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0001058	PMID:23692737	PCS		2/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0031869	PMID:23692737	PCS		2/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0002650	PMID:23692737;PMID:15728585	PCS		8/9			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0004322	PMID:23692737;PMID:15728585	PCS		11/12			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0010648	PMID:23692737	PCS		2/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0000023	PMID:23692737	PCS		1/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0001382	PMID:17206620;PMID:15728585	PCS		17/17			P	HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0000592	PMID:23692737;PMID:17206620;PMID:15728585	PCS		12/12		HP:0012825	P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0001290	PMID:23692737	PCS		2/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0011463	PMID:23692737	PCS		2/2			C	HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0025019	PMID:23692737	PCS		1/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0000978	PMID:23692737	PCS		2/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0002757	PMID:23692737;PMID:17206620;PMID:15728585	PCS		12/12			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0001631	PMID:23692737	PCS		1/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0000974	PMID:23692737	PCS		2/2			P	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0004349	PMID:17206620;PMID:15728585	PCS		7/7			P	HPO:probinson[2021-01-30]
OMIM:619115	Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1		HP:0000006	PMID:15728585	PCS					I	HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:609306	Spinocerebellar ataxia 26		HP:0002311	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0002078	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0000639	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0001151	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0001272	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0001260	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0002066	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0003581	OMIM:609306	TAS					C	HPO:probinson[2013-03-10]
OMIM:609306	Spinocerebellar ataxia 26		HP:0002070	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0000641	OMIM:609306	IEA					P	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0000006	OMIM:609306	IEA					I	HPO:iea[2009-02-17]
OMIM:609306	Spinocerebellar ataxia 26		HP:0003677	OMIM:609306	IEA					C	HPO:iea[2009-02-17]
OMIM:620794	Deafness, autosomal recessive 124		HP:0003577	PMID:38459354	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620794	Deafness, autosomal recessive 124		HP:0001751	PMID:38459354	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620794	Deafness, autosomal recessive 124		HP:0000407	PMID:38459354	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620794	Deafness, autosomal recessive 124		HP:0000007	PMID:38459354	PCS					I	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620794	Deafness, autosomal recessive 124		HP:0001626	PMID:38459354	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620794	Deafness, autosomal recessive 124		HP:0001249	PMID:38459354	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620794	Deafness, autosomal recessive 124		HP:0000478	PMID:38459354	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:126800	Duane retraction syndrome 1		HP:0000486	PMID:29133973	PCS	HP:0003577				P	HP:probinson[2018-09-01]
OMIM:126800	Duane retraction syndrome 1		HP:0000661	PMID:29133973	PCS					P	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:126800	Duane retraction syndrome 1		HP:0000619	OMIM:126800	TAS					P	HPO:iea[2009-02-17]
OMIM:126800	Duane retraction syndrome 1		HP:0000634	PMID:12395297	PCS					P	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:126800	Duane retraction syndrome 1		HP:0000565	PMID:29133973	PCS					P	HP:probinson[2018-09-01]
OMIM:126800	Duane retraction syndrome 1		HP:0000542	PMID:12395297	PCS					P	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:126800	Duane retraction syndrome 1		HP:0009921	PMID:29133973	PCS	HP:0003577				P	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:126800	Duane retraction syndrome 1		HP:0000006	PMID:9781021	PCS					I	HPO:iea[2009-02-17];HP:probinson[2018-09-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0005227	PMID:7661930	PCS					P	HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0003003	PMID:17557300	PCS					P	HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0009592	PMID:22692065	PCS		1/3			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0012174	PMID:7661930	PCS					P	HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0001274	PMID:22692065	PCS		3/3			P	HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0000007	PMID:7661930	PCS					I	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0002282	PMID:22692065	PCS		2/3			P	HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0007565	PMID:7661930	PCS					P	HPO:probinson[2021-01-01]
OMIM:619101	Mismatch repair cancer syndrome 4		HP:0012539	PMID:22692065	PCS					P	HPO:probinson[2021-01-01]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000483	PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0010749	PMID:33807164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0003577	PMID:33807164	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0005214	PMID:33807164;PMID:32006683;PMID:31792352	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000189	PMID:31792352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000343	PMID:33807164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000023	PMID:33807164;PMID:32006683;PMID:31792352	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0010648	PMID:33807164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0001252	PMID:33807164;PMID:32006683;PMID:31792352	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0002580	PMID:33807164;PMID:32006683;PMID:31792352	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0003593	PMID:31792352	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0001508	PMID:33807164;PMID:32006683;PMID:31792352	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0100822	PMID:32006683	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000678	PMID:33807164;PMID:32006683;PMID:31792352	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0002933	PMID:33807164;PMID:32006683;PMID:31792352	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000978	PMID:33807164;PMID:32006683;PMID:31792352	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000218	PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0002714	PMID:33807164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000015	PMID:33807164;PMID:32006683;PMID:31792352	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0001763	PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0100808	PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000776	PMID:33807164;PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000973	PMID:33807164;PMID:32006683;PMID:31792352	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000275	PMID:33807164;PMID:32006683	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0001166	PMID:32006683;PMID:31792352	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000098	PMID:33807164;PMID:32006683;PMID:31792352	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000494	PMID:32006683;PMID:31792352	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0002650	PMID:33807164;PMID:32006683;PMID:31792352	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000276	PMID:33807164;PMID:32006683	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0002035	PMID:32006683	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0001382	PMID:33807164;PMID:32006683;PMID:31792352	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0002253	PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0011003	PMID:33807164;PMID:32006683;PMID:31792352	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0032446	PMID:33807164;PMID:32006683;PMID:31792352	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0100541	PMID:31792352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0010811	PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0025193	PMID:32006683;PMID:31792352	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0009890	PMID:33807164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0100775	PMID:31792352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000506	PMID:33807164;PMID:32006683	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000508	PMID:33807164;PMID:32006683;PMID:31792352	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0007651	PMID:32006683;PMID:31792352	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000767	PMID:33807164;PMID:32006683;PMID:31792352	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000689	PMID:33807164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000007	PMID:32006683	PCS					I	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0005616	PMID:32006683;PMID:31792352	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000400	PMID:32006683	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620780	Cutis laxa, autosomal recessive, type ID		HP:0000963	PMID:33807164;PMID:32006683;PMID:31792352	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:187770	Thoracopelvic dysostosis		HP:0004322	OMIM:187770	IEA					P	HPO:iea[2009-02-17]
OMIM:187770	Thoracopelvic dysostosis		HP:0000773	OMIM:187770	IEA					P	HPO:iea[2009-02-17]
OMIM:187770	Thoracopelvic dysostosis		HP:0000006	OMIM:187770	IEA					I	HPO:iea[2009-02-17]
OMIM:187770	Thoracopelvic dysostosis		HP:0002643	OMIM:187770	IEA					P	HPO:iea[2009-02-17]
OMIM:602247	Xanthomatosis, susceptibility to		HP:0003124	OMIM:602247	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602247	Xanthomatosis, susceptibility to		HP:0000991	OMIM:602247	IEA					P	HPO:skoehler[2015-01-21]
OMIM:602247	Xanthomatosis, susceptibility to		HP:0000006	OMIM:602247	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:602247	Xanthomatosis, susceptibility to		HP:0000951	OMIM:602247	IEA					P	HPO:iea[2009-02-17]
OMIM:614343	Intellectual developmental disorder, autosomal recessive 19		HP:0000750	PMID:21629298	PCS		0/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:614343	Intellectual developmental disorder, autosomal recessive 19		HP:0000007	PMID:21629298	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:614343	Intellectual developmental disorder, autosomal recessive 19		HP:0001270	PMID:21629298	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003477	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003434	PMID:12565911	PCS					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001250	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003198	PMID:12565911	PCS					P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002066	PMID:12565911	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003551	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002460	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001251	PMID:12565911	PCS		4/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0033685	PMID:12565911	PCS		1/3			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003390	PMID:12565911	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0031987	OMIM:607459	IEA					P	HPO:skoehler[2019-02-22]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0007240	PMID:12565911	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000639	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000716	PMID:12565911	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000518	OMIM:607459	TAS		HP:0040283			P	HPO:iea[2012-04-28]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000712	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003701	PMID:12565911	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001324	PMID:12565911	PCS		7/7			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003548	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000597	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003700	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002578	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003546	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001644	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003202	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001265	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003324	PMID:12565911	PCS					P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003687	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003200	PMID:12565911	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0006858	PMID:12565911	PCS					P	HPO:probinson[2012-04-28];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003487	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002076	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0006937	PMID:12565911	PCS					P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001260	PMID:12565911	PCS		5/8			P	HPO:probinson[2022-03-27];HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002151	OMIM:607459	TAS				HP:0012825	P	HPO:probinson[2012-04-28]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0010871	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000407	PMID:12565911	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000726	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000007	PMID:12565911	PCS					I	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003713	PMID:12565911	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001653	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003438	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001611	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001336	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003557	PMID:12565911	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0007814	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0033748	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001751	PMID:12565911	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0004389	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001310	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003691	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0030319	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0010546	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0100543	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0007344	OMIM:607459	IEA					P	HPO:iea[2009-02-17]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001824	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002359	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003688	PMID:12565911	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003689	PMID:12565911	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002015	PMID:12565911	PCS		3/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002136	PMID:12565911	PCS					P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003621	PMID:12565911	PCS		1/7			C	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001761	PMID:12565911	PCS		1/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000590	PMID:12565911	PCS		1/1			P	HPO:iea[2012-04-28];HPO:probinson[2022-03-25]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0003581	PMID:12565911	PCS		6/7			C	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001284	PMID:12565911	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002093	PMID:12565911	PCS		2/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0008180	PMID:12565911	PCS		1/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0025708	PMID:12565911	PCS		1/1			C	HPO:probinson[2022-03-25]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000508	PMID:12565911	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0002403	PMID:12565911	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0006886	PMID:12565911	PCS					P	HPO:probinson[2012-04-28];HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0001634	PMID:12565911	PCS		3/7			P	HPO:probinson[2022-03-27]
OMIM:607459	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis		HP:0000544	PMID:12565911	PCS		6/7			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000054	OMIM:610125	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000175	OMIM:610125	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610125	Microphthalmia, syndromic 5		HP:0004322	OMIM:610125	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610125	Microphthalmia, syndromic 5		HP:0001250	OMIM:610125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0001382	OMIM:610125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000482	OMIM:610125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0001263	OMIM:610125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0001252	OMIM:610125	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610125	Microphthalmia, syndromic 5		HP:0011755	OMIM:610125	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610125	Microphthalmia, syndromic 5		HP:0001290	OMIM:610125	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000609	OMIM:610125	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000518	OMIM:610125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000528	OMIM:610125	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000568	OMIM:610125	IEA					P	HPO:skoehler[2015-01-21]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000589	OMIM:610125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000556	OMIM:610125	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000006	OMIM:610125	TAS					I	HPO:skoehler[2012-10-17]
OMIM:610125	Microphthalmia, syndromic 5		HP:0000028	OMIM:610125	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0003202	PMID:26945885	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0002015	PMID:26945885	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0003596	PMID:26945885	PCS		2/3			C	HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0002340	PMID:26945885	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0002483	PMID:26945885	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0003584	PMID:26945885	PCS		1/3			C	HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0001260	PMID:26945885	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0002273	PMID:26945885	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0410170	PMID:26945885	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0002093	PMID:26945885	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0007354	PMID:26945885	PCS		3/3			P	HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0001257	PMID:26945885	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0000006	PMID:26945885	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:617892	Amyotrophic lateral sclerosis, susceptibility to, 24		HP:0001347	PMID:26945885	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0004322	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0410031	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0001290	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0011456	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0410030	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0010442	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000319	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0001763	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000175	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000252	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0002474	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0011968	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000293	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0001263	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000294	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0009890	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000407	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000448	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0004209	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0001417	PMID:28296084	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000520	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000322	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000369	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000325	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0010628	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0004467	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000384	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000340	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0003577	PMID:28296084	PCS		1/1			C	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000343	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0004383	OMIM:301022	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0001508	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0008551	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000414	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000219	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0002317	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0007665	OMIM:301022	IEA					P	HPO:skoehler[2019-09-07]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000413	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000776	OMIM:301022	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000750	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0002650	PMID:28296084	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000431	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0031936	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000193	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0001680	OMIM:301022	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0005280	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0011624	PMID:28296084	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0002007	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0007018	OMIM:301022	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:301022	Neurodevelopmental disorder, X-linked, with craniofacial abnormalities		HP:0000347	OMIM:301022	IEA					P	HPO:skoehler[2019-04-18]
OMIM:120040	Cochleosaccular degeneration of the inner ear with progressive cataracts		HP:0000365	OMIM:120040	IEA					P	HPO:iea[2009-02-17]
OMIM:120040	Cochleosaccular degeneration of the inner ear with progressive cataracts		HP:0000707	OMIM:120040	IEA					P	HPO:iea[2009-02-17]
OMIM:120040	Cochleosaccular degeneration of the inner ear with progressive cataracts		HP:0000006	OMIM:120040	IEA					I	HPO:iea[2009-02-17]
OMIM:120040	Cochleosaccular degeneration of the inner ear with progressive cataracts		HP:0007834	OMIM:120040	IEA					P	HPO:iea[2009-02-17]
OMIM:620569	Leber-like hereditary optic neuropathy, autosomal recessive 2		HP:0003621	PMID:28031252	PCS		2/3			C	HPO:probinson[2024-03-13]
OMIM:620569	Leber-like hereditary optic neuropathy, autosomal recessive 2		HP:0025709	PMID:28031252	PCS		1/3			C	HPO:probinson[2024-03-13]
OMIM:620569	Leber-like hereditary optic neuropathy, autosomal recessive 2		HP:0000529	PMID:28031252	PCS		3/3			P	HPO:probinson[2024-03-13]
OMIM:620569	Leber-like hereditary optic neuropathy, autosomal recessive 2		HP:0000007	PMID:28031252	PCS					I	HPO:probinson[2024-03-13]
OMIM:620569	Leber-like hereditary optic neuropathy, autosomal recessive 2		HP:0000648	PMID:28031252	PCS		3/3			P	HPO:probinson[2024-03-13]
OMIM:620569	Leber-like hereditary optic neuropathy, autosomal recessive 2		HP:0000576	PMID:28031252	PCS		3/3			P	HPO:probinson[2024-03-13]
OMIM:620569	Leber-like hereditary optic neuropathy, autosomal recessive 2		HP:0000642	PMID:28031252	PCS		3/3			P	HPO:probinson[2024-03-13]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001176	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002980	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000046	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002780	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0003154	PMID:14758361	PCS		1/3		HP:0012825	P	HPO:probinson[2020-04-27];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0003031	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000041	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0003351	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000085	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0011410	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002937	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000316	PMID:14758361	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001769	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0009702	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001601	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0020206	OMIM:201750	TAS					P	HPO:probinson[2020-04-27]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002974	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000252	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000054	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000453	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000013	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001586	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000452	PMID:14758361	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002153	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0003041	PMID:14758361	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0011800	PMID:14758361	PCS		1/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0032569	OMIM:201750	IEA					P	HPO:skoehler[2019-09-07]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0033812	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0012385	OMIM:201750	TAS					P	HPO:skoehler[2013-10-22]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0008163	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002308	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002902	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000007	PMID:14758361	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000846	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000405	OMIM:201750	TAS					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0008368	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000048	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000047	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000520	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000248	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000369	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000445	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000066	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000062	OMIM:201750	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001195	PMID:14758361;OMIM:201750	PCS		20/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0025486	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0008072	OMIM:201750	IEA					H	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0008073	OMIM:201750	IEA					H	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0008233	OMIM:201750	TAS					P	HPO:probinson[2020-04-27]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001943	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0025436	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000256	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001623	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002676	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000138	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001545	OMIM:201750	TAS					P	HPO:probinson[2020-04-27]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001166	PMID:14758361	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001562	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001363	PMID:14758361	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002650	PMID:14758361;OMIM:201750	PCS		11/13			P	HPO:probinson[2023-01-21];HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000272	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0031213	PMID:14758361	PCS		1/1			P	HPO:probinson[2020-04-27];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0031214	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0005280	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0031216	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001838	PMID:14758361	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0009473	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0001518	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000822	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0008665	PMID:14758361	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-21]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0002007	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000147	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000028	OMIM:201750	IEA					P	HPO:iea[2009-02-17]
OMIM:201750	Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis		HP:0000786	PMID:14758361	PCS		1/3			P	HPO:probinson[2023-01-21]
OMIM:614814	Adams-Oliver syndrome 3		HP:0011917	PMID:22883147	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0000252	PMID:22883147	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0003577	PMID:22883147	PCS		6/6			C	HPO:probinson[2022-09-11];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0004279	PMID:22883147	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0001057	PMID:22883147	PCS	HP:0003577	2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0012745	PMID:22883147	PCS		1/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0004691	PMID:22883147	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0002194	PMID:22883147	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0010743	PMID:22883147	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0010760	PMID:22883147	PCS		1/6			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0008398	PMID:22883147	PCS		1/6			P	HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0009882	PMID:22883147	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:614814	Adams-Oliver syndrome 3		HP:0000006	PMID:22883147	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-11]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0007737	PMID:15781871	PCS	HP:0011462	1/2			P	HPO:probinson[2022-12-20]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0000662	PMID:15781871	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0012047	OMIM:257270	TAS					P	HPO:skoehler[2012-10-17]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0011463	PMID:15781871	PCS		3/3			C	HPO:probinson[2022-12-20]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0000007	PMID:15781871	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0007642	PMID:15781871	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-20]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0000545	PMID:15781871	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:257270	Night blindness, congenital stationary, type 1B		HP:0000666	PMID:15781871	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:608583	Atrial fibrillation, familial, 1		HP:0001727	PMID:9070470	PCS		2/10			P	HPO:probinson[2012-04-10];HPO:probinson[2022-07-10]
OMIM:608583	Atrial fibrillation, familial, 1		HP:0011463	PMID:9070470	PCS					C	HPO:probinson[2022-07-10]
OMIM:608583	Atrial fibrillation, familial, 1		HP:0003581	PMID:9070470	PCS					C	HPO:probinson[2022-07-10]
OMIM:608583	Atrial fibrillation, familial, 1		HP:0005110	PMID:9070470	PCS					P	HPO:probinson[2012-04-10];HPO:probinson[2022-07-10]
OMIM:608583	Atrial fibrillation, familial, 1		HP:0000006	PMID:9070470	PCS					I	HPO:probinson[2012-04-10];HPO:probinson[2022-07-10]
OMIM:205250	Amyotrophic lateral sclerosis with polyglucosan bodies		HP:0003202	OMIM:205250	TAS					P	HPO:probinson[2012-04-25]
OMIM:205250	Amyotrophic lateral sclerosis with polyglucosan bodies		HP:0002483	OMIM:205250	TAS					P	HPO:probinson[2012-04-25]
OMIM:205250	Amyotrophic lateral sclerosis with polyglucosan bodies		HP:0002460	OMIM:205250	TAS					P	HPO:probinson[2012-04-25]
OMIM:205250	Amyotrophic lateral sclerosis with polyglucosan bodies		HP:0007354	OMIM:205250	TAS					P	HPO:probinson[2012-04-25]
OMIM:205250	Amyotrophic lateral sclerosis with polyglucosan bodies		HP:0000007	OMIM:205250	TAS					I	HPO:probinson[2012-04-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0001696	PMID:31534215;PMID:30148830	IEA		7/11			P	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0001651	PMID:30148830	PCS	HP:0030674	1/4			P	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0001651	PMID:31534215	PCS		5/7			P	HPO:probinson[2020-08-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0030674	PMID:31534215	PCS					C	HPO:probinson[2020-08-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0003251	PMID:30148830	PCS		3/3	MALE		P	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0001746	PMID:31534215	PCS		1/7			P	HPO:probinson[2020-08-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0000007	PMID:30148830	PCS					I	HPO:probinson[2020-08-25];HPO:probinson[2020-08-25]
OMIM:618948	Heterotaxy, visceral, 9, autosomal, with male infertility		HP:0000403	PMID:31534215	PCS		1/6			P	HPO:probinson[2020-08-25]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0000705	OMIM:245660	IEA					P	HPO:iea[2009-02-17]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0034363	PMID:12915477	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0006297	PMID:12915477	PCS		6/6			P	HPO:probinson[2022-05-12]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0430007	PMID:12915477	PCS		1/6			P	HPO:probinson[2022-05-12]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0000007	PMID:12915477	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-12]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0001615	PMID:12915477	PCS	HP:0003623	6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-12]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0008404	PMID:12915477	PCS		6/6			P	HPO:probinson[2022-05-12]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0001612	OMIM:245660	IEA					P	HPO:iea[2009-02-17]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0008390	OMIM:245660	IEA					P	HPO:iea[2009-02-17]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0200042	OMIM:245660	IEA					P	HPO:skoehler[2010-06-20]
OMIM:245660	Laryngoonychocutaneous syndrome		HP:0003623	PMID:12915477	PCS		6/6			C	HPO:probinson[2022-05-12]
OMIM:613809	Retinitis pigmentosa 39		HP:0007737	OMIM:613809	TAS					P	HPO:probinson[2013-08-10]
OMIM:613809	Retinitis pigmentosa 39		HP:0001123	OMIM:613809	TAS					P	HPO:probinson[2013-08-10]
OMIM:613809	Retinitis pigmentosa 39		HP:0000007	PMID:10775529	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:613809	Retinitis pigmentosa 39		HP:0000505	OMIM:613809	TAS					P	HPO:probinson[2013-08-10]
OMIM:613809	Retinitis pigmentosa 39		HP:0000510	PMID:10775529	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-20]
OMIM:613809	Retinitis pigmentosa 39		HP:0007843	OMIM:613809	TAS					P	HPO:probinson[2013-08-10]
OMIM:613809	Retinitis pigmentosa 39		HP:0000512	OMIM:613809	TAS					P	HPO:probinson[2013-08-10]
OMIM:145800	Hypertrophia musculorum vera		HP:0008981	OMIM:145800	IEA					P	HPO:iea[2009-02-17]
OMIM:145800	Hypertrophia musculorum vera		HP:0000006	OMIM:145800	IEA					I	HPO:iea[2009-02-17]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0004322	OMIM:132450	TAS					P	HPO:skoehler[2013-02-25]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0002673	OMIM:132450	TAS					P	HPO:skoehler[2013-05-31]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0001156	OMIM:132450	TAS					P	HPO:skoehler[2014-11-26]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0000160	OMIM:132450	TAS					P	HPO:skoehler[2014-11-26]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0030672	OMIM:132450	TAS					P	HPO:skoehler[2015-12-30]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0012368	OMIM:132450	TAS					P	HPO:skoehler[2013-10-22]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0030329	OMIM:132450	TAS					P	HPO:skoehler[2015-04-26]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0000518	OMIM:132450	TAS					P	HPO:skoehler[2009-02-17]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0000405	OMIM:132450	IEA					P	HPO:iea[2009-02-17]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0002857	OMIM:132450	TAS					P	HPO:skoehler[2013-02-25]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0002656	OMIM:132450	IEA					P	HPO:iea[2009-02-17]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0000311	OMIM:132450	TAS					P	HPO:skoehler[2013-02-25]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0000006	OMIM:132450	IEA					I	HPO:iea[2009-02-17]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0000545	OMIM:132450	IEA					P	HPO:iea[2009-02-17]
OMIM:132450	Epiphyseal dysplasia, multiple, with myopia and conductive deafness		HP:0009803	OMIM:132450	TAS					P	HPO:skoehler[2013-02-25]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000286	PMID:20577004	PCS		22/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000341	PMID:20577004	PCS		31/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0002983	PMID:20577004	PCS		34/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000343	PMID:20577004	PCS		28/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000486	PMID:20577004	PCS		9/34			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0001156	PMID:20577004	PCS		34/34			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000540	PMID:20577004	PCS		3/34			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0004322	PMID:20577004	PCS		34/34			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0001252	PMID:20577004	PCS		28/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0011516	PMID:20577004	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0010669	PMID:20577004	PCS		33/34			P	HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0010055	PMID:20577004	PCS		26/34			P	HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000316	PMID:20577004	PCS		5/34			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000954	PMID:20577004	PCS		5/34			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0007663	PMID:20577004	PCS				HP:0003676	P	HPO:skoehler[2015-07-26];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0200068	PMID:20577004	PCS					P	HPO:skoehler[2013-05-31];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0008897	PMID:20577004	PCS		34/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0001620	PMID:20577004	PCS		32/34			P	HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000973	PMID:20577004	PCS		34/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0002213	PMID:20577004	PCS		25/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000574	PMID:20577004	PCS		24/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000233	PMID:20577004	PCS		28/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0002750	PMID:20577004	PCS		14/34			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000276	PMID:20577004	PCS		33/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0002057	PMID:20577004	PCS		31/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000470	PMID:20577004	PCS		30/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0011447	PMID:20577004	PCS		22/22			P	HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000007	PMID:20577004	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000648	PMID:20577004	PCS		34/34			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0001852	PMID:20577004	PCS		26/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0001159	PMID:20577004	PCS		2/34			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000520	PMID:20577004	PCS		31/34			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000248	PMID:20577004	PCS		30/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000545	PMID:20577004	PCS		12/34			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-02]
OMIM:614800	Short stature, optic nerve atrophy, and pelger-huet anomaly		HP:0000324	PMID:20577004	PCS		24/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0001682	OMIM:108900	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0001684	OMIM:108900	TAS					P	HPO:probinson[2013-04-07]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0001629	OMIM:108900	TAS		HP:0040283			P	HPO:skoehler[2012-10-12]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0005110	OMIM:108900	TAS					P	HPO:skoehler[2012-10-12]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0001636	OMIM:108900	TAS		HP:0040283			P	HPO:skoehler[2012-10-12]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0001712	OMIM:108900	TAS		HP:0040283			P	HPO:skoehler[2012-10-12]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0004935	OMIM:108900	TAS		HP:0040283			P	HPO:skoehler[2012-10-12]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0000006	OMIM:108900	TAS					I	HPO:probinson[2009-02-17]
OMIM:108900	Atrial septal defect with atrioventricular conduction defects		HP:0012248	OMIM:108900	TAS					P	HPO:probinson[2013-04-07]
OMIM:602092	Deafness, neurosensory, autosomal recessive 18		HP:0000407	PMID:12107438	PCS					P	HPO:skoehler[2010-06-18]
OMIM:602092	Deafness, neurosensory, autosomal recessive 18		HP:0000007	PMID:12107438	PCS					I	HPO:lccarmody[2009-02-17]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0003577	PMID:15317751	PCS		23/23			C	HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0001036	PMID:15317751	PCS		6/23			P	HPO:skoehler[2013-01-21];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0025092	PMID:15317751	PCS				HP:0012826	P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0040162	PMID:15317751	PCS					P	HPO:probinson[2021-10-13];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0000958	PMID:17557927	PCS					P	HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0040189	PMID:17557927	PCS					P	HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0000656	PMID:17557927	PCS		HP:0040283			P	HPO:skoehler[2013-01-21];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0000007	PMID:15317751	PCS					I	HPO:skoehler[2013-01-21];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0001019	PMID:15317751	PCS		6/23			P	HPO:skoehler[2013-01-21];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0000966	PMID:17557927	PCS		HP:0040283			P	HPO:skoehler[2013-01-21];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0007479	PMID:15317751;PMID:17557927	PCS		17/50			P	HPO:probinson[2021-10-13];HPO:skoehler[2013-01-09];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0000982	PMID:15317751	PCS		23/23			P	HPO:skoehler[2013-01-21];HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0007503	PMID:15317751	PCS		6/23			P	HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0007503	PMID:17557927	PCS	HP:0003593	27/27			P	HPO:probinson[2021-10-13]
OMIM:612281	Ichthyosis, congenital, autosomal recessive 6		HP:0000962	PMID:15317751	PCS		6/23			P	HPO:skoehler[2013-01-21];HPO:probinson[2021-10-13]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0012727	PMID:17994018	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0004970	PMID:17994018	PCS		18/92			P	HPO:probinson[2021-05-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0011834	PMID:19409525	PCS					P	HPO:probinson[2013-04-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0500007	PMID:17994018	PCS					P	HPO:probinson[2021-05-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0012499	PMID:17994018	PCS		13/92			P	HPO:probinson[2021-05-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0004933	PMID:17994018;PMID:19409525	PCS		46/102			P	HPO:probinson[2013-04-02];HPO:probinson[2021-05-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0005181	PMID:19409525	PCS		26/127			P	HPO:probinson[2013-04-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0000006	PMID:19409525	PCS					I	HPO:probinson[2013-01-09]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0033505	PMID:17994018	PCS					P	HPO:probinson[2021-05-02]
OMIM:611788	Aortic aneurysm, familial thoracic 6		HP:0004942	PMID:19409525	PCS					P	HPO:probinson[2013-04-02]
OMIM:137500	Giant neutrophil leukocytes		HP:0001871	OMIM:137500	IEA					P	HPO:iea[2009-02-17]
OMIM:137500	Giant neutrophil leukocytes		HP:0000006	OMIM:137500	IEA					I	HPO:iea[2009-02-17]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0007737	PMID:26494905	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0025066	PMID:26494905	PCS		3/3			P	HPO:probinson[2017-06-24];HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0004445	PMID:26494905	PCS		1/3			P	HPO:skoehler[2017-07-13]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0000662	PMID:26494905	PCS		3/3			P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0100014	PMID:26494905	PCS					P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0001903	PMID:26494905	PCS					P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0011463	PMID:26494905	PCS		1/3			C	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0007843	PMID:26494905	PCS		2/3			P	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0007722	PMID:26494905	PCS					P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0001105	PMID:26494905	PCS		3/3			P	HPO:probinson[2017-06-24];HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0003621	PMID:26494905	PCS		1/3			C	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0001882	PMID:26494905	PCS		0/3			P	HPO:probinson[2017-06-24];HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0030609	PMID:26494905	PCS		3/3			P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0030529	PMID:26494905	PCS					P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0011273	PMID:26494905	PCS		2/3			P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0025709	PMID:26494905	PCS		1/3			C	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0040303	PMID:26494905	PCS					P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0025708	PMID:26494905	PCS		1/3			C	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0040049	PMID:26494905	PCS		2/3			P	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0200070	PMID:26494905	PCS		2/3			P	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0032231	PMID:26494905	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0000007	PMID:26494905	PCS					I	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0000543	PMID:26494905	PCS		2/3			P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0001873	PMID:26494905	PCS		0/3			P	HPO:probinson[2017-06-24];HPO:probinson[2024-03-15]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0000545	PMID:26494905	PCS					P	HPO:probinson[2017-06-24]
OMIM:616959	Retinitis pigmentosa and erythrocytic microcytosis		HP:0004447	PMID:26494905	PCS		1/3			P	HPO:skoehler[2017-07-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001254	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0003577	PMID:34952832	PCS		3/13			C	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0000582	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002202	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001396	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0030830	PMID:34952832	PCS		3/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002783	PMID:34952832	PCS		13/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001252	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0003593	PMID:34952832	PCS		3/13			C	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002020	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002240	PMID:34952832	PCS		4/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0033542	PMID:34952832	PCS		2/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0030718	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001270	PMID:34952832	PCS		3/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0034315	PMID:34952832	PCS		5/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0003270	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0100750	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0100721	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001508	PMID:34952832	PCS		13/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0011463	PMID:34952832	PCS		2/13			C	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0011220	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0034388	PMID:34952832	PCS		5/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0006530	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0000219	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001269	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0003623	PMID:34952832	PCS		5/13			C	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002875	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002013	PMID:34952832	PCS		2/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002110	PMID:34952832	PCS		4/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002099	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001263	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0025179	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002094	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0012735	PMID:34952832	PCS		4/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0030828	PMID:34952832	PCS		2/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002092	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0012236	PMID:34952832	PCS		0/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0005180	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0000007	PMID:34952832	PCS					I	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0000403	PMID:34952832	PCS		3/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001634	PMID:34952832	PCS		1/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0002028	PMID:34952832	PCS		5/13			P	HPO:probinson[2023-04-13]
OMIM:620233	Respiratory infections, recurrent, and failure to thrive with or without diarrhea		HP:0001974	PMID:34952832	PCS		2/13			P	HPO:probinson[2023-04-13]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0004322	OMIM:212710	IEA					P	HPO:iea[2009-02-17]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0001271	OMIM:212710	IEA					P	HPO:iea[2009-02-17]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0000519	OMIM:212710	IEA					P	HPO:iea[2009-02-17]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0001251	OMIM:212710	IEA					P	HPO:iea[2009-02-17]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0001284	OMIM:212710	IEA					P	HPO:iea[2009-02-17]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0000007	OMIM:212710	IEA					I	HPO:iea[2009-02-17]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0002936	OMIM:212710	IEA					P	HPO:iea[2009-02-17]
OMIM:212710	Cataract-Ataxia-Deafness-Retardation syndrome		HP:0008615	OMIM:212710	IEA	HP:0003584				P	HPO:iea[2009-02-17]
OMIM:616781	Joubert syndrome 25		HP:0001321	OMIM:616781	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616781	Joubert syndrome 25		HP:0001263	PMID:26477546	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616781	Joubert syndrome 25		HP:0001251	PMID:26477546	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616781	Joubert syndrome 25		HP:0003593	OMIM:616781	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616781	Joubert syndrome 25		HP:0000657	PMID:26477546	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616781	Joubert syndrome 25		HP:0001290	PMID:26477546	PCS		2/3			P	HPO:probinson[2017-06-17]
OMIM:616781	Joubert syndrome 25		HP:0000007	PMID:26477546	PCS					I	HPO:probinson[2017-06-17]
OMIM:616781	Joubert syndrome 25		HP:0002419	PMID:26477546	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616781	Joubert syndrome 25		HP:0000512	PMID:26477546	PCS		1/3			P	HPO:probinson[2017-06-17]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000286	PMID:31794431	PCS		2/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000582	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000540	PMID:31794431	PCS		3/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0001250	PMID:31794431	PCS		5/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0010862	PMID:31794431	PCS		8/8			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0001629	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0012471	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0007165	PMID:31794431	PCS		3/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0001845	PMID:31794431	PCS		2/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0008872	PMID:31794431	PCS	HP:0003593	3/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0002119	PMID:31794431	PCS		4/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0002714	PMID:31794431	PCS					P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0001643	PMID:31794431	PCS	HP:0003577	1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000750	PMID:31794431	PCS		9/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0002079	PMID:31794431	PCS		2/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0001263	PMID:31794431	PCS					P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0002194	PMID:31794431	PCS		9/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0005280	PMID:31794431	PCS		2/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000506	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000729	PMID:31794431	PCS		2/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000426	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000601	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0004209	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000565	PMID:31794431	PCS		2/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0001631	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0007018	PMID:31794431	PCS		1/9			P	HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000006	PMID:31794431	PCS					I	HPO:probinson[2020-09-11];HPO:probinson[2020-09-11]
OMIM:618974	Li-Ghorgani-Weisz-Hubshman syndrome		HP:0000369	PMID:31794431	PCS		3/9			P	HPO:probinson[2020-09-11]
OMIM:133000	Erythema palmare hereditarium		HP:0010783	OMIM:133000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:133000	Erythema palmare hereditarium		HP:0000006	OMIM:133000	IEA					I	HPO:iea[2009-02-17]
OMIM:614196	Nephrotic syndrome, type 6		HP:0003774	PMID:21722858	PCS		1/5			P	HPO:probinson[2023-03-31]
OMIM:614196	Nephrotic syndrome, type 6		HP:0003621	PMID:21722858	PCS		5/5			C	HPO:probinson[2023-03-31]
OMIM:614196	Nephrotic syndrome, type 6		HP:0000100	PMID:21722858	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:614196	Nephrotic syndrome, type 6		HP:0005576	PMID:21722858	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-31]
OMIM:614196	Nephrotic syndrome, type 6		HP:0000969	PMID:21722858	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-31]
OMIM:614196	Nephrotic syndrome, type 6		HP:0000097	PMID:21722858	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-31]
OMIM:614196	Nephrotic syndrome, type 6		HP:0003073	PMID:21722858	PCS		5/5			P	HPO:skoehler[2012-10-17]
OMIM:614196	Nephrotic syndrome, type 6		HP:0000007	PMID:21722858	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-31]
OMIM:614196	Nephrotic syndrome, type 6		HP:0000093	PMID:21722858	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-31]
OMIM:614196	Nephrotic syndrome, type 6		HP:0012579	PMID:21722858	PCS		1/2			P	HPO:probinson[2023-03-31]
OMIM:613835	Leber congenital amaurosis 8		HP:0000550	PMID:11231775	PCS		7/12			P	HPO:probinson[2013-02-23];HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0000563	PMID:11231775	PCS		2/19			P	HPO:probinson[2013-02-23];HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0000490	OMIM:613835	TAS					P	HPO:skoehler[2019-09-07]
OMIM:613835	Leber congenital amaurosis 8		HP:0001483	PMID:16543197	PCS		3/3			P	HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0003593	PMID:16543197;PMID:11231775	PCS		21/22			C	HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0000580	PMID:16543197	PCS		1/3			P	HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0030505	PMID:16543197;PMID:11231775	PCS		10/17			P	HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0000518	OMIM:613835	TAS					P	HPO:probinson[2013-02-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0000639	PMID:11231775	PCS		18/19			P	HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0011463	PMID:16543197	PCS		1/3			C	HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0008499	PMID:16543197;PMID:11231775	PCS		15/22			P	HPO:probinson[2013-02-23];HPO:probinson[2022-04-23];HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0000007	PMID:11231775	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0007663	PMID:16543197;PMID:11231775	PCS		22/22			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-23];HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0030491	PMID:11231775	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0001116	PMID:11231775	PCS		3/19			P	HPO:probinson[2022-04-23]
OMIM:613835	Leber congenital amaurosis 8		HP:0000533	PMID:16543197	PCS		1/3			P	HPO:probinson[2022-04-23]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0003676	PMID:15269180	PCS					C	HPO:skoehler[2012-12-02];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0000640	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001310	PMID:15269180	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001332	PMID:15269180	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001272	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0003693	OMIM:604391	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0002066	PMID:15269180	PCS		1/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001252	PMID:15269180	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001251	PMID:15269180	PCS		2/2			P	HPO:probinson[2022-12-20];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0002061	OMIM:604391	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0011463	PMID:15269180	PCS		1/2			C	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0007286	PMID:15269180	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0000657	PMID:15269180	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001009	PMID:15269180	PCS		0/2			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0002317	PMID:15269180	PCS		2/2			P	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0002359	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001265	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0000571	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0003621	PMID:15269180	PCS		1/2			C	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0000750	PMID:15269180	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001266	PMID:15269180	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001260	PMID:15269180	PCS		2/2			P	HPO:skoehler[2012-12-02];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0002075	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0002072	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0011133	OMIM:604391	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0007772	OMIM:604391	TAS					P	HPO:skoehler[2012-12-02]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0000007	PMID:10612394	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0003438	PMID:15269180	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:604391	Ataxia-telangiectasia-like disorder 1		HP:0001315	PMID:15269180	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:200300	Acetophenetidin sensitivity		HP:0001871	OMIM:200300	IEA					P	HPO:iea[2009-02-17]
OMIM:200300	Acetophenetidin sensitivity		HP:0001878	PMID:6015912	PCS					P	HPO:lccarmody[2018-10-18]
OMIM:200300	Acetophenetidin sensitivity		HP:0000007	OMIM:200300	IEA					I	HPO:iea[2009-02-17]
OMIM:200300	Acetophenetidin sensitivity		HP:0012119	PMID:6015912	PCS					P	HPO:skoehler[2012-10-17];HPO:lccarmody[2018-10-18]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0003577	PMID:14556245	IEA		2/2			C	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0002100	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0004322	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0001274	PMID:14556245	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0001629	PMID:14556245	PCS	HP:0003577	1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000639	PMID:14556245	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0012450	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000612	PMID:14556245	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000337	PMID:14556245	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000218	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0006532	PMID:14556245	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000378	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0001643	PMID:14556245	PCS	HP:0003623	1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000256	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000278	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000410	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0001249	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000494	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000475	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000453	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000193	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000394	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000470	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000407	PMID:14556245	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0001419	PMID:14556245	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000767	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000426	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000348	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000505	PMID:14556245	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0002944	PMID:14556245	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0008689	PMID:14556245	PCS		1/2			P	HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000369	PMID:14556245	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300472	Corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia		HP:0000588	PMID:14556245	PCS		1/2			P	HPO:probinson[2012-07-17];HPO:probinson[2021-09-25]
OMIM:620227	Deafness, autosomal dominant 85		HP:0003577	PMID:34059922	PCS		1/8			C	HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0003621	PMID:34059922	PCS		1/8			C	HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0003596	PMID:34059922	PCS		4/8			C	HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0000407	PMID:34059922	PCS		8/9			P	HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0011463	PMID:34059922	PCS		1/8			C	HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0011462	PMID:34059922	PCS		1/8			C	HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0003829	PMID:34059922	PCS					I	HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0034585	PMID:34059922	PCS		1/9			P	HPO:probinson[2023-06-10]
OMIM:620227	Deafness, autosomal dominant 85		HP:0000006	PMID:34059922	PCS					I	HPO:probinson[2023-06-10]
OMIM:616795	Spinocerebellar ataxia 42		HP:0002015	PMID:26456284	IEA		4/15			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0000651	PMID:26456284	PCS					P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0003487	OMIM:616795	PCS		4/15			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0002497	PMID:26456284	PCS					P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0000012	PMID:26456284	PCS		4/14			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0001272	PMID:26456284	PCS					P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0001260	PMID:26456284	PCS		12/15			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0006938	PMID:26456284	PCS		6/13			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0000020	PMID:26456284	PCS		2/14			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0001251	PMID:26456284	PCS		15/15			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0001152	PMID:26456284	PCS		6/15			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0002064	PMID:26456284	PCS		4/13			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0031166	OMIM:616795	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616795	Spinocerebellar ataxia 42		HP:0100543	PMID:26456284	PCS					P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0000716	PMID:26456284	PCS		13/25			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0007001	PMID:26456284	PCS					P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0007256	PMID:26456284	PCS					P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0002317	PMID:26456284	PCS		19/25			P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0000006	PMID:26456284	PCS					I	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0000666	PMID:26456284	PCS					P	HPO:probinson[2017-06-18]
OMIM:616795	Spinocerebellar ataxia 42		HP:0003677	OMIM:616795	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616795	Spinocerebellar ataxia 42		HP:0001337	OMIM:616795	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616795	Spinocerebellar ataxia 42		HP:0001347	OMIM:616795	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:618960	Mitchell syndrome		HP:0001298	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0002015	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0002312	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0001344	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0001288	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0001250	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0003690	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0003390	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0012332	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0002747	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0012391	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0000006	PMID:32169171	PCS					I	HPO:probinson[2020-08-27];HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0002522	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:618960	Mitchell syndrome		HP:0002500	PMID:32169171	PCS					P	HPO:probinson[2020-08-27]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0000121	PMID:9062355	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0003158	PMID:9062355	PCS		6/6			P	HPO:probinson[2021-07-12]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0003126	PMID:9062355	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0003355	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0004322	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0000083	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0025466	PMID:9062355	PCS		10/10			P	HPO:probinson[2021-07-12]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0000097	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0003076	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0002150	PMID:9062355	PCS		6/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0000092	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0002907	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0001419	PMID:9062355	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0000114	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0002148	OMIM:308990	IEA					P	HPO:iea[2009-02-17]
OMIM:308990	Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis		HP:0003677	OMIM:308990	IEA					C	HPO:iea[2009-02-17]
OMIM:611944	Lymphatic malformation 2		HP:0011463	OMIM:611944	TAS					C	HPO:probinson[2021-07-14]
OMIM:611944	Lymphatic malformation 2		HP:0003829	OMIM:611944	IEA					I	HPO:skoehler[2010-06-19]
OMIM:611944	Lymphatic malformation 2		HP:0001004	OMIM:611944	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611944	Lymphatic malformation 2		HP:0000006	OMIM:611944	IEA					I	HPO:skoehler[2010-06-19]
OMIM:249700	Langer mesomelic dysplasia		HP:0003027	OMIM:249700	IEA					P	HPO:iea[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0003038	PMID:17394206	PCS		0/1			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:249700	Langer mesomelic dysplasia		HP:0003993	OMIM:249700	TAS					P	HPO:skoehler[2013-06-03]
OMIM:249700	Langer mesomelic dysplasia		HP:0003102	PMID:17394206	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:249700	Langer mesomelic dysplasia		HP:0003022	OMIM:249700	TAS					P	HPO:probinson[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0003067	PMID:17394206	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:249700	Langer mesomelic dysplasia		HP:0004991	PMID:17394206	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:249700	Langer mesomelic dysplasia		HP:0005011	PMID:17394206	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:249700	Langer mesomelic dysplasia		HP:0100864	OMIM:249700	IEA					P	HPO:iea[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0006381	OMIM:249700	IEA					P	HPO:iea[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0002938	OMIM:249700	IEA					P	HPO:iea[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0000007	OMIM:249700	IEA					I	HPO:iea[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0000218	PMID:17394206	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:249700	Langer mesomelic dysplasia		HP:0002986	OMIM:249700	TAS					P	HPO:probinson[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0005736	OMIM:249700	IEA					P	HPO:iea[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0000347	OMIM:249700	IEA					P	HPO:iea[2009-02-17]
OMIM:249700	Langer mesomelic dysplasia		HP:0002984	OMIM:249700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:249700	Langer mesomelic dysplasia		HP:0001249	PMID:17394206	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-16]
OMIM:249700	Langer mesomelic dysplasia		HP:0008845	PMID:17394206	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:602086	Arrhythmogenic right ventricular dysplasia, familial, 3		HP:0003140	OMIM:602086	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602086	Arrhythmogenic right ventricular dysplasia, familial, 3		HP:0004308	OMIM:602086	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602086	Arrhythmogenic right ventricular dysplasia, familial, 3		HP:0011663	OMIM:602086	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602086	Arrhythmogenic right ventricular dysplasia, familial, 3		HP:0003338	OMIM:602086	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602086	Arrhythmogenic right ventricular dysplasia, familial, 3		HP:0000006	OMIM:602086	TAS					I	HPO:skoehler[2009-02-17]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0003202	PMID:21343608	PCS		1/1			P	HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0034529	OMIM:615511	TAS					P	HPO:probinson[2023-03-31]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0003750	PMID:1631143	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0003201	PMID:1631143	PCS		1/10		HP:0033198	P	HPO:skoehler[2014-08-24];HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0003198	PMID:21343608	PCS		1/1			P	HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0001252	PMID:21343608	PCS		1/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0001284	PMID:21343608	PCS		1/1			P	HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0003738	PMID:1631143	PCS		8/10			P	HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0000007	PMID:1631143	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-01-27]
OMIM:615511	Myopathy due to myoadenylate deaminase deficiency		HP:0001324	PMID:1631143;PMID:21343608	PCS		11/11			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-01-27];HPO:probinson[2021-01-27]
OMIM:603373	Hyperthyroidism, familial gestational		HP:0012188	PMID:9854118	TAS		1/1			H	HPO:probinson[2013-03-30];HPO:probinson[2020-12-05]
OMIM:603373	Hyperthyroidism, familial gestational		HP:0031506	PMID:9854118	PCS		1/1		HP:0025221	P	HPO:probinson[2020-12-05]
OMIM:603373	Hyperthyroidism, familial gestational		HP:0000836	PMID:9854118	TAS		1/1		HP:0025221	P	HPO:probinson[2013-03-30];HPO:probinson[2020-12-05]
OMIM:603373	Hyperthyroidism, familial gestational		HP:0031098	PMID:9854118	PCS		1/1		HP:0025221	P	HPO:probinson[2020-12-05]
OMIM:603373	Hyperthyroidism, familial gestational		HP:0001649	PMID:9854118	PCS		1/1		HP:0025221	P	HPO:probinson[2020-12-05]
OMIM:603373	Hyperthyroidism, familial gestational		HP:0000006	PMID:9854118	TAS					I	HPO:probinson[2013-01-09]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0004325	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0002389	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0004467	PMID:27889061	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0003577	PMID:27889061	PCS		2/2			C	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0004322	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0012805	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0001252	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000482	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0004482	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000518	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0011002	PMID:27889061	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0011001	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000007	PMID:27889061	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000568	PMID:27889061	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0004209	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0002007	PMID:27889061	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0007513	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000256	PMID:27889061	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000586	PMID:27889061	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000589	PMID:27889061	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0008527	PMID:27889061	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000347	PMID:27889061	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617306	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness		HP:0000358	PMID:27889061	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:607115	Cinca syndrome		HP:0033308	PMID:12928894	PCS		2/3			P	HPO:probinson[2020-12-07]
OMIM:607115	Cinca syndrome		HP:0000365	PMID:12483741	PCS		2/6			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001250	PMID:12483741	PCS		1/6			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0003593	PMID:12032915	PCS		2/8			C	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0011463	PMID:12032915	PCS		1/8			C	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001903	PMID:12483741	PCS		6/6			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0002716	PMID:12483741	PCS		6/6			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0000554	PMID:12483741	PCS		2/6			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001004	PMID:12928894	PCS		1/3			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001369	PMID:12032915;PMID:12928894	PCS		9/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-31];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0003623	PMID:12032915	PCS		5/8			C	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001287	PMID:12032915;PMID:12483741	PCS		11/14			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-10-31];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0003565	PMID:12928894;PMID:12483741	PCS		9/9			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001880	PMID:12483741	PCS		4/6			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001085	PMID:12928894;PMID:12483741	PCS		8/9			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0011227	PMID:12928894	PCS		3/3			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0000408	PMID:12928894	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001954	PMID:12032915;PMID:12928894;PMID:12483741	PCS		18/19			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0000988	PMID:12032915	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0000988	PMID:12928894	PCS	HP:0003577	3/3			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0002007	PMID:12032915;PMID:12928894	PCS		12/13			P	HPO:probinson[2020-10-31];HPO:skoehler[2017-07-13];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001510	PMID:12483741	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0000520	PMID:12032915	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001433	PMID:12483741	PCS		6/6			P	HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0000006	PMID:12032915	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-31]
OMIM:607115	Cinca syndrome		HP:0001974	PMID:12483741	PCS		6/6			P	HPO:probinson[2020-10-31]
OMIM:611777	Brugada syndrome 2		HP:0001663	PMID:17967977	PCS					P	HPO:probinson[2013-04-02]
OMIM:611777	Brugada syndrome 2		HP:0011705	PMID:17967977	PCS					P	HPO:probinson[2013-04-02]
OMIM:611777	Brugada syndrome 2		HP:0011712	PMID:17967977	PCS					P	HPO:probinson[2013-04-02]
OMIM:611777	Brugada syndrome 2		HP:0001279	PMID:17967977	PCS					P	HPO:probinson[2013-04-02]
OMIM:611777	Brugada syndrome 2		HP:0000006	PMID:17967977	PCS					I	HPO:probinson[2013-01-09]
OMIM:611777	Brugada syndrome 2		HP:0001645	PMID:17967977	PCS		HP:0040283			P	HPO:probinson[2013-04-02]
OMIM:611777	Brugada syndrome 2		HP:0012248	PMID:11839626	PCS		7/12			P	HPO:probinson[2013-04-07]
OMIM:601202	Cataract, anterior polar, 2		HP:0001134	PMID:8852669	PCS	HP:0003593	17/17			P	HPO:lccarmody[2018-06-13]
OMIM:601202	Cataract, anterior polar, 2		HP:0000646	PMID:8852669	PCS	HP:0003593	16/17			P	HPO:lccarmody[2018-06-13]
OMIM:601202	Cataract, anterior polar, 2		HP:0011501	PMID:8852669	PCS		0/17			P	HPO:lccarmody[2018-06-13];HPO:probinson[2024-03-09]
OMIM:601202	Cataract, anterior polar, 2		HP:0000006	PMID:8852669	PCS					I	HPO:lccarmody[2018-06-13]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001371	OMIM:608540	IEA					P	HPO:iea[2009-02-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001250	OMIM:608540	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001252	OMIM:608540	IEA					P	HPO:iea[2009-02-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0002240	PMID:14973778	PCS	HP:0034197	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001790	PMID:14973778	PCS	HP:0034197	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001290	OMIM:608540	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0010841	PMID:14973778	PCS		1/1			P	HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0000316	PMID:14973778	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0000239	PMID:14973778	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001522	PMID:14973778	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0000135	PMID:14973778	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001744	PMID:14973778	PCS	HP:0034197	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0003642	PMID:14973778	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0002059	OMIM:608540	IEA					P	HPO:iea[2009-02-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0000252	OMIM:608540	IEA					P	HPO:iea[2009-02-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0000233	OMIM:608540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001560	OMIM:608540	IEA					P	HPO:iea[2009-02-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001263	OMIM:608540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001284	PMID:14973778	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0034392	PMID:14973778	PCS	HP:0003577	1/1			P	HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0034197	PMID:14973778	PCS		1/1			C	HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0000007	PMID:14973778	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001638	PMID:14973778	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0001511	OMIM:608540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608540	Congenital disorder of glycosylation, type Ik		HP:0000347	PMID:14973778	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:617460	Retinitis pigmentosa 79		HP:0001133	PMID:25190649	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0003621	PMID:25190649	PCS		1/8			C	HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0007737	PMID:25190649	PCS					P	HPO:probinson[2022-11-24];HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0000662	PMID:25190649	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0011463	PMID:25190649	PCS		1/8			C	HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0011462	PMID:25190649	PCS		6/8			C	HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0000613	PMID:25190649	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0007663	PMID:25190649	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0007401	OMIM:617460	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617460	Retinitis pigmentosa 79		HP:0000543	PMID:25190649	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0007843	PMID:25190649	PCS					P	HPO:probinson[2022-11-24]
OMIM:617460	Retinitis pigmentosa 79		HP:0000006	PMID:25190649	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0004325	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000252	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000750	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0004322	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0002750	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000100	OMIM:613606	IEA					P	HPO:skoehler[2019-09-07]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000490	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0001263	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000939	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000426	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000007	OMIM:613606	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000400	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0002007	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0001510	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0001873	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613606	Forsythe-Wakeling syndrome		HP:0000369	OMIM:613606	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612518	Ciliary dyskinesia, primary, 10		HP:0012265	PMID:19052621	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-24]
OMIM:612518	Ciliary dyskinesia, primary, 10		HP:0001696	PMID:19052621	PCS		2/3			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612518	Ciliary dyskinesia, primary, 10		HP:0000007	PMID:19052621	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612518	Ciliary dyskinesia, primary, 10		HP:0005938	PMID:19052621	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2020-07-24]
OMIM:612518	Ciliary dyskinesia, primary, 10		HP:0000389	PMID:19052621	PCS		3/3			P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-24]
OMIM:612518	Ciliary dyskinesia, primary, 10		HP:0011109	PMID:19052621	TAS		3/3			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:612518	Ciliary dyskinesia, primary, 10		HP:0011108	PMID:19052621	TAS					P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-24]
OMIM:278250	Wrinkly skin syndrome		HP:0000286	PMID:24815019	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0007517	OMIM:278250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:278250	Wrinkly skin syndrome		HP:0001374	PMID:24815019	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000684	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0004322	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001252	OMIM:278250	TAS					P	HPO:probinson[2009-02-17]
OMIM:278250	Wrinkly skin syndrome		HP:0006191	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001808	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000319	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000316	PMID:24815019	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0002812	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001763	PMID:24815019	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0005328	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0001249	OMIM:278250	IEA					P	HPO:iea[2009-02-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000253	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000252	OMIM:278250	IEA					P	HPO:iea[2009-02-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000494	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001382	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001582	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000691	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0003160	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001537	PMID:24815019	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000767	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000007	PMID:18157129	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000369	PMID:24815019	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0001611	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0030799	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0003577	PMID:24815019	PCS		1/1			C	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000343	PMID:24815019	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0001476	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000023	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000260	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0003691	OMIM:278250	TAS					P	HPO:probinson[2009-02-17]
OMIM:278250	Wrinkly skin syndrome		HP:0008070	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0011995	OMIM:278250	TAS					P	HPO:probinson[2012-07-21]
OMIM:278250	Wrinkly skin syndrome		HP:0001508	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000938	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0009004	OMIM:278250	IEA					P	HPO:iea[2009-02-17]
OMIM:278250	Wrinkly skin syndrome		HP:0001869	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000218	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001788	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000670	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000431	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001762	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0002650	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000750	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0003100	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000270	OMIM:278250	TAS					P	HPO:skoehler[2015-06-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000592	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0011623	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0000308	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0002808	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0002645	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:278250	Wrinkly skin syndrome		HP:0001511	PMID:24815019	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:278250	Wrinkly skin syndrome		HP:0007414	OMIM:278250	IEA					P	HPO:iea[2009-02-17]
OMIM:278250	Wrinkly skin syndrome		HP:0001799	OMIM:278250	TAS					P	HPO:skoehler[2015-06-22]
OMIM:278250	Wrinkly skin syndrome		HP:0000028	OMIM:278250	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615277	Cataract 19, multiple types		HP:0000639	OMIM:615277	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615277	Cataract 19, multiple types		HP:0007780	PMID:11917274	PCS					P	HPO:probinson[2015-05-12]
OMIM:615277	Cataract 19, multiple types		HP:0000646	OMIM:615277	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615277	Cataract 19, multiple types		HP:0000007	PMID:11917274	PCS					I	HPO:probinson[2015-05-12]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0000011	PMID:23228021	PCS		2/7			P	HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0002059	PMID:23228021	PCS		1/7			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0000252	PMID:23228021	PCS		6/7			P	HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0002078	PMID:23228021	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0000750	PMID:23228021	PCS		7/7			P	HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0000365	PMID:23228021	PCS		2/7			P	HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0004322	PMID:23228021	PCS		5/7			P	HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0001272	PMID:23228021	PCS		2/7			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0001252	PMID:23228021	PCS		7/7			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0001270	PMID:23228021	PCS		7/7			P	HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0012301	PMID:23228021	PCS					P	HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0007366	PMID:19690088	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0000007	PMID:23228021	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-08-11]
OMIM:613612	Congenital disorder of glycosylation, type IIi		HP:0001249	PMID:23228021	PCS		7/7			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-11]
OMIM:125851	Maturity-onset diabetes of the young, type II		HP:0003621	PMID:1570017	PCS		7/7			C	HPO:probinson[2023-04-10]
OMIM:125851	Maturity-onset diabetes of the young, type II		HP:0004904	PMID:1570017	PCS		16/16			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-04-10]
OMIM:125851	Maturity-onset diabetes of the young, type II		HP:0000006	PMID:1570017	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2023-04-10]
OMIM:601216	Dental anomalies and short stature		HP:0002650	PMID:19344874	PCS					P	HPO:probinson[2022-10-10]
OMIM:601216	Dental anomalies and short stature		HP:0002750	OMIM:601216	IEA					P	HPO:iea[2009-02-17]
OMIM:601216	Dental anomalies and short stature		HP:0004322	PMID:19344874	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:601216	Dental anomalies and short stature		HP:0000691	OMIM:601216	TAS					P	HPO:skoehler[2015-08-02]
OMIM:601216	Dental anomalies and short stature		HP:0000705	OMIM:601216	IEA					P	HPO:iea[2009-02-17]
OMIM:601216	Dental anomalies and short stature		HP:0008450	OMIM:601216	IEA					P	HPO:iea[2009-02-17]
OMIM:601216	Dental anomalies and short stature		HP:0008441	OMIM:601216	IEA					P	HPO:iea[2009-02-17]
OMIM:601216	Dental anomalies and short stature		HP:0000926	OMIM:601216	IEA					P	HPO:iea[2009-02-17]
OMIM:601216	Dental anomalies and short stature		HP:0000998	OMIM:601216	TAS					P	HPO:skoehler[2015-12-30]
OMIM:601216	Dental anomalies and short stature		HP:0000327	OMIM:601216	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:601216	Dental anomalies and short stature		HP:0000007	PMID:19344874	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:601216	Dental anomalies and short stature		HP:0002945	OMIM:601216	IEA					P	HPO:iea[2009-02-17]
OMIM:601216	Dental anomalies and short stature		HP:0000303	OMIM:601216	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:601216	Dental anomalies and short stature		HP:0001634	OMIM:601216	TAS					P	HPO:skoehler[2015-12-30]
OMIM:601216	Dental anomalies and short stature		HP:0000677	PMID:19344874	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:601216	Dental anomalies and short stature		HP:0000687	OMIM:601216	TAS					P	HPO:skoehler[2015-08-02]
OMIM:606579	Vitiligo-Associated multiple autoimmune disease susceptibility 1		HP:0001045	PMID:20526340	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2022-03-21]
OMIM:606579	Vitiligo-Associated multiple autoimmune disease susceptibility 1		HP:0010982	PMID:20526340	PCS					I	HPO:probinson[2013-02-25];HPO:probinson[2022-03-21]
OMIM:106050	Angioma serpiginosum, autosomal dominant		HP:0003621	OMIM:106050	IEA					C	HPO:iea[2009-02-17]
OMIM:106050	Angioma serpiginosum, autosomal dominant		HP:0003745	OMIM:106050	IEA					I	HPO:iea[2009-02-17]
OMIM:106050	Angioma serpiginosum, autosomal dominant		HP:0000006	OMIM:106050	IEA					I	HPO:iea[2009-02-17]
OMIM:106050	Angioma serpiginosum, autosomal dominant		HP:0003677	OMIM:106050	IEA					C	HPO:iea[2009-02-17]
OMIM:106050	Angioma serpiginosum, autosomal dominant		HP:0000962	OMIM:106050	IEA					P	HPO:iea[2009-02-17]
OMIM:618021	Tetraamelia syndrome 2		HP:0005304	PMID:29769720	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0009827	PMID:29769720	PCS		7/7			P	HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0000054	PMID:29769720	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0000175	PMID:29769720	PCS		6/7			P	HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0003577	PMID:29769720	PCS		7/7			C	HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0002561	PMID:29769720	PCS		1/7			P	HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0000162	PMID:29769720	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0100336	PMID:29769720	PCS		4/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0001629	OMIM:618021	TAS					P	HPO:skoehler[2019-02-15]
OMIM:618021	Tetraamelia syndrome 2		HP:0000308	PMID:29769720	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0010296	PMID:29769720	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0000316	PMID:29769720	PCS		1/7			P	HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0000007	PMID:29769720	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0000369	OMIM:618021	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618021	Tetraamelia syndrome 2		HP:0000347	PMID:29769720	PCS		11/17			P	HPO:probinson[2022-10-18];HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618021	Tetraamelia syndrome 2		HP:0005944	PMID:29769720	PCS		5/7			P	HPO:probinson[2022-10-18]
OMIM:607101	Deafness, autosomal recessive 30		HP:0000408	OMIM:607101	TAS					P	HPO:skoehler[2015-12-30]
OMIM:607101	Deafness, autosomal recessive 30		HP:0000007	PMID:12032315	PCS					I	HPO:probinson[2013-01-09]
OMIM:607101	Deafness, autosomal recessive 30		HP:0001730	PMID:12032315	PCS					P	HPO:probinson[2013-03-02]
OMIM:138800	Goiter, multinodular 1		HP:0002895	OMIM:138800	IEA					P	HPO:iea[2009-02-17]
OMIM:138800	Goiter, multinodular 1		HP:0000866	OMIM:138800	IEA					P	HPO:iea[2009-02-17]
OMIM:138800	Goiter, multinodular 1		HP:0000006	OMIM:138800	IEA					I	HPO:iea[2009-02-17]
OMIM:608232	Leukemia, chronic myeloid		HP:0004852	OMIM:608232	TAS					P	HP:probinson[2018-04-05]
OMIM:608232	Leukemia, chronic myeloid		HP:0001442	OMIM:608232	TAS					I	HPO:skoehler[2012-10-17]
OMIM:608232	Leukemia, chronic myeloid		HP:0004848	OMIM:608232	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608232	Leukemia, chronic myeloid		HP:0005506	OMIM:608232	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602079	Trimethylaminuria		HP:0000716	PMID:9398858	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-05]
OMIM:602079	Trimethylaminuria		HP:0001903	OMIM:602079	IEA					P	HPO:iea[2009-02-17]
OMIM:602079	Trimethylaminuria		HP:0000822	OMIM:602079	TAS				HP:0033789	P	HPO:probinson[2009-02-17]
OMIM:602079	Trimethylaminuria		HP:0000007	PMID:9398858	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-05]
OMIM:602079	Trimethylaminuria		HP:0001649	OMIM:602079	TAS				HP:0033789	P	HPO:probinson[2009-02-17]
OMIM:602079	Trimethylaminuria		HP:0006532	OMIM:602079	IEA					P	HPO:iea[2009-02-17]
OMIM:602079	Trimethylaminuria		HP:0003614	PMID:9398858	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-05]
OMIM:602079	Trimethylaminuria		HP:0001744	OMIM:602079	IEA					P	HPO:iea[2009-02-17]
OMIM:602079	Trimethylaminuria		HP:0001875	OMIM:602079	IEA					P	HPO:iea[2009-02-17]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0001696	PMID:24055112	PCS		9/14			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0002110	PMID:24055112	PCS		6/12			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0033036	PMID:24055112	PCS		8/8			P	HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0011108	PMID:24055112	PCS		10/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0200073	PMID:24055112	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0012265	PMID:24055112	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0012255	PMID:24055112	PCS		14/14			P	HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0012384	OMIM:615505	TAS				HP:0031796	P	HPO:skoehler[2013-11-18]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0000007	PMID:24055112	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0000403	PMID:24055112	PCS		9/11			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0002205	PMID:24055112	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0002643	PMID:24055112	PCS	HP:0003623	11/13			P	HPO:probinson[2022-03-26]
OMIM:615505	Ciliary dyskinesia, primary, 28		HP:0004469	PMID:24055112	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-26]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000286	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000341	PMID:19052029	PCS		2/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000483	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001176	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000582	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000486	PMID:19052029	PCS		1/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001250	PMID:19052029	PCS		2/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001274	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000581	OMIM:613174	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001252	PMID:19052029	PCS		3/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0002162	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000262	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0012745	PMID:19052029	PCS		2/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0008070	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000316	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000954	PMID:19052029	PCS		2/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000337	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000414	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0100807	PMID:19052029	PCS		3/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000733	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000637	PMID:19052029	PCS		1/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0002714	PMID:19052029	PCS		1/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000218	PMID:19052029	PCS		3/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0009765	PMID:19052029	PCS		1/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0003745	OMIM:613174	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000256	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001249	PMID:19052029	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000358	PMID:19052029	PCS		1/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000577	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001363	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000076	PMID:19052029	PCS		1/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0002650	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000431	PMID:19052029	PCS		2/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001263	PMID:19052029	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001518	PMID:19052029	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000601	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0001833	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000722	PMID:19052029	PCS		1/6			P	HPO:skoehler[2014-03-24]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0100716	PMID:19052029	PCS		1/5			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000565	PMID:19052029	PCS		1/6			P	HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0002007	PMID:19052029	PCS		2/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000520	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000322	PMID:19052029	PCS		3/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000248	PMID:19052029	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:613174	Chromosome 5p13 duplication syndrome		HP:0000369	PMID:19052029	PCS		3/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-01]
OMIM:175900	Porokeratosis 3, multiple types		HP:0003621	OMIM:175900	TAS					C	HPO:probinson[2023-01-18];HPO:probinson[2023-01-18]
OMIM:175900	Porokeratosis 3, multiple types		HP:0001036	OMIM:175900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:175900	Porokeratosis 3, multiple types		HP:0200044	OMIM:175900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:175900	Porokeratosis 3, multiple types		HP:0008404	OMIM:175900	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:175900	Porokeratosis 3, multiple types		HP:0000006	PMID:22983302	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-18]
OMIM:618009	Intellectual developmental disorder 61		HP:0000154	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000750	PMID:29740699	PCS		13/13			P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000431	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0001263	PMID:29740699	PCS	HP:0003593	13/13			P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0001252	PMID:29740699	PCS		3/13			P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0045025	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0002194	PMID:29740699	PCS		6/13			P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000319	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000729	PMID:29740699	PCS		5/13			P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0011098	PMID:29740699	PCS		3/13			P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0012450	PMID:29740699	PCS		4/13			P	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000629	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000316	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000426	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000219	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0011170	PMID:29740699	PCS	HP:0011463	1/13			P	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000664	PMID:29740699	PCS					P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0007018	PMID:29740699	PCS		3/13			P	HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0009921	PMID:29740699	PCS	HP:0003577	2/13			P	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:618009	Intellectual developmental disorder 61		HP:0000006	PMID:29740699	PCS					I	HPO:probinson[2020-04-06];HPO:probinson[2020-04-06]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0000175	OMIM:183700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0001770	OMIM:183700	IEA					P	HPO:iea[2009-02-17]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0005321	OMIM:183700	IEA					P	HPO:iea[2009-02-17]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0000272	OMIM:183700	IEA					P	HPO:iea[2009-02-17]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0001839	OMIM:183700	IEA					P	HPO:iea[2009-02-17]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0001171	OMIM:183700	IEA					P	HPO:iea[2009-02-17]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0000598	OMIM:183700	IEA					P	HPO:iea[2009-02-17]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0000347	OMIM:183700	IEA					P	HPO:iea[2009-02-17]
OMIM:183700	Split-Foot deformity with mandibulofacial dysostosis		HP:0000006	OMIM:183700	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0000230	PMID:16960814	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0100511	PMID:16960814	PCS		0/8			P	HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0031817	PMID:16960814	PCS		0/8			P	HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0000509	PMID:16960814	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0025520	PMID:16960814	PCS		8/8			P	HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0004363	PMID:16960814	PCS		0/8			P	HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0003593	PMID:16960814	PCS		8/8			C	HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0000007	PMID:16960814	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:610455	Tumoral calcinosis, normophosphatemic, familial		HP:0100529	PMID:16960814	PCS		0/8			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-14]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0002069	PMID:28794249	PCS		9/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0002487	PMID:28794249	PCS		4/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0010849	PMID:28794249	PCS		3/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0002540	PMID:28794249	PCS		9/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001332	PMID:28794249	PCS		4/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0002121	PMID:28794249	PCS		3/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0000160	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001252	PMID:28794249	PCS		9/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0003593	PMID:28794249	PCS		9/9			C	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001251	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0032794	PMID:28794249	PCS		7/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0010841	PMID:28794249	PCS		9/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0000639	PMID:28794249	PCS		2/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0100702	PMID:28794249	PCS		2/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0000316	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0000733	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001348	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0025517	PMID:28794249	PCS		5/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0008936	PMID:28794249	PCS		5/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0006813	PMID:28794249	PCS		2/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001344	PMID:28794249	PCS		8/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0002650	PMID:28794249	PCS		2/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001266	PMID:28794249	PCS		5/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001263	PMID:28794249	PCS	HP:0003593	9/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0002072	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0010533	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0031475	PMID:28794249	PCS		4/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0033258	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0011097	PMID:28794249	PCS		5/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0011471	PMID:28794249	PCS		9/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0011150	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0032792	PMID:28794249	PCS		5/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0000348	PMID:28794249	PCS		1/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0007359	PMID:28794249	PCS		6/9			P	HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0000006	PMID:28794249	PCS					I	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619317	Developmental and epileptic encephalopathy 6B, non-Dravet		HP:0001336	PMID:28794249	PCS		6/9			P	HPO:probinson[2021-07-04]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0001166	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000582	PMID:21248748	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0002474	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000490	PMID:21248748	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0001263	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0010863	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0012758	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0100783	PMID:21248748	PCS	HP:0003577				P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000319	PMID:21248748	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000717	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000316	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000337	PMID:21248748	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000219	PMID:21248748	PCS					P	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0001466	OMIM:612242	TAS					I	HPO:probinson[2017-06-21]
OMIM:612242	Chromosome 10q22.3-q23.2 deletion syndrome		HP:0000256	PMID:20345475	PCS					P	HPO:probinson[2017-06-21]
OMIM:103100	Adie pupil		HP:0001265	OMIM:103100	IEA					P	HPO:iea[2009-02-17]
OMIM:103100	Adie pupil		HP:0012074	OMIM:103100	TAS					P	HPO:skoehler[2015-01-21]
OMIM:103100	Adie pupil		HP:0000006	OMIM:103100	IEA					I	HPO:iea[2009-02-17]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001133	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000483	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0003577	PMID:24290075	PCS		1/1			C	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000662	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000662	PMID:25168386	PCS	HP:0003621	2/2			P	HPO:probinson[2021-10-13];HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000540	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0012841	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0002516	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000510	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000510	PMID:25168386	PCS	HP:0003621	2/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000510	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001841	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0002910	PMID:25168386	PCS		2/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000054	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000750	PMID:25168386	PCS	HP:0011463	2/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0003124	PMID:25168386	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001085	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001162	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0002099	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001263	PMID:26763875	PCS		2/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0004691	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000093	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0100259	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0100259	PMID:25168386	PCS	HP:0003577	1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0012047	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000007	PMID:24290075	PCS					I	HPO:probinson[2021-10-13];HPO:probinson[2022-12-03]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0000026	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001631	PMID:24290075	PCS		1/1			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0008689	PMID:26763875	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001513	PMID:25168386;PMID:26763875;PMID:24290075	PCS		5/5			P	HPO:probinson[2021-10-13]
OMIM:619471	Bardet-Biedl syndrome 20		HP:0001733	PMID:25168386	PCS		1/2			P	HPO:probinson[2021-10-13]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001332	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001272	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001250	OMIM:610333	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0002240	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0003593	OMIM:610333	TAS					C	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0000238	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0002119	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0002514	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0002910	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0002415	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001744	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0000253	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0002059	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0011968	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0200149	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0011344	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0002093	OMIM:610333	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0003819	PMID:16845400	PCS					C	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0000007	PMID:16845400	PCS					I	HPO:probinson[2013-01-09]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001511	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0000444	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001257	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001873	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001433	PMID:16845400	PCS					P	HPO:probinson[2013-04-06]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0000369	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:610333	Aicardi-Goutieres syndrome 4		HP:0001876	OMIM:610333	TAS					P	HPO:skoehler[2013-11-18]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0003477	PMID:33497358	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0011284	PMID:33497358	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0001762	PMID:33497358	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0000407	PMID:33497358	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0000508	PMID:33497358	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0012450	PMID:33497358	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0003593	PMID:33497358	PCS		2/2			C	HPO:probinson[2021-10-20]
OMIM:619465	Visceral neuropathy, familial, 2, autosomal recessive		HP:0000007	PMID:33497358	PCS					I	HPO:probinson[2021-10-20];HPO:probinson[2021-10-20]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0000486	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002540	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0004322	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001332	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002123	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001250	PMID:26424145	PCS		5/8			P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001252	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001251	OMIM:616756	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002061	PMID:26424145	PCS		6/8			P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001290	OMIM:616756	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0012448	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002938	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002515	PMID:26424145	PCS		3/8			P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0000556	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001249	OMIM:616756	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002136	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002059	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0000252	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001762	PMID:26424145	PCS		2/8			P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002650	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002376	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002079	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001263	PMID:26424145	PCS					P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0000407	PMID:26424145	PCS		3/8			P	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002808	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0002827	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0000007	PMID:26424145	IEA					I	HPO:probinson[2017-06-17]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0001513	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616756	Spastic paraplegia and psychomotor retardation with or without seizures		HP:0000545	OMIM:616756	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0003577	PMID:11773004	PCS		8/8			C	HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0000970	PMID:19890349	PCS		3/3			P	HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0002046	PMID:19890349	PCS		1/3			P	HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0010783	OMIM:606545	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0008064	PMID:19890349	IEA		3/3			P	HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0033252	PMID:19890349	PCS		1/3			P	HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0012472	PMID:11773004	PCS		1/8			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0000007	PMID:11773004	PCS					I	HPO:probinson[2013-09-14];HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0000656	PMID:19890349;PMID:11773004	PCS		2/11			P	HPO:probinson[2022-03-16];HPO:skoehler[2015-08-16];HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0000966	OMIM:606545	TAS					P	HPO:skoehler[2015-08-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0007479	PMID:11773004	PCS		8/8			P	HPO:probinson[2013-09-14];HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0000982	PMID:11773004	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:606545	Ichthyosis, congenital, autosomal recessive 3		HP:0000962	OMIM:606545	TAS					P	HPO:probinson[2013-09-14]
OMIM:230200	Galactokinase deficiency with cataracts		HP:0012023	OMIM:230200	TAS					P	HPO:probinson[2012-07-27]
OMIM:230200	Galactokinase deficiency with cataracts		HP:0012024	OMIM:230200	TAS					P	HPO:probinson[2012-07-27]
OMIM:230200	Galactokinase deficiency with cataracts		HP:0000518	OMIM:230200	TAS					P	HPO:probinson[2009-02-17]
OMIM:230200	Galactokinase deficiency with cataracts		HP:0000007	OMIM:230200	TAS					I	HPO:probinson[2009-02-17]
OMIM:230200	Galactokinase deficiency with cataracts		HP:6000723	PMID:7670469	PCS		2/2			P	HPO:probinson[2024-06-29]
OMIM:230200	Galactokinase deficiency with cataracts		HP:0002516	OMIM:230200	TAS		HP:0040283			P	HPO:probinson[2014-01-19]
OMIM:230200	Galactokinase deficiency with cataracts		HP:0006579	OMIM:230200	IEA					P	HPO:iea[2009-02-17]
OMIM:604352	Febrile seizures, familial, 4		HP:0002069	OMIM:604352	IEA					P	HPO:iea[2009-02-17]
OMIM:604352	Febrile seizures, familial, 4		HP:0002373	OMIM:604352	TAS					P	HPO:probinson[2009-02-17]
OMIM:604352	Febrile seizures, familial, 4		HP:0010819	OMIM:604352	IEA					P	HPO:iea[2009-02-17]
OMIM:604352	Febrile seizures, familial, 4		HP:0011463	OMIM:604352	TAS					C	HPO:probinson[2013-12-19]
OMIM:604352	Febrile seizures, familial, 4		HP:0010818	OMIM:604352	IEA					P	HPO:iea[2009-02-17]
OMIM:604352	Febrile seizures, familial, 4		HP:0003593	OMIM:604352	TAS					C	HPO:probinson[2009-02-17]
OMIM:604352	Febrile seizures, familial, 4		HP:0000006	OMIM:604352	IEA					I	HPO:iea[2009-02-17]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0011939	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0010804	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0004322	PMID:17873649	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000243	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001250	PMID:17873649	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000280	PMID:17873649	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0045075	PMID:17873649	PCS		1/2			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0012471	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000316	PMID:17873649	PCS		3/4			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0003745	PMID:17873649	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001249	OMIM:612530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000175	PMID:17873649	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000252	PMID:17873649	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000494	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000490	OMIM:612530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001263	OMIM:612530	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000767	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000601	OMIM:612530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000568	OMIM:612530	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001852	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000322	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000006	PMID:19184110	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000204	OMIM:612530	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000369	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000687	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000341	PMID:17873649	PCS		3/4			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000384	OMIM:612530	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000582	PMID:17873649	PCS		1/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001792	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0002089	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000463	PMID:17873649	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0002002	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001629	PMID:17873649	PCS	HP:0003577	1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0008551	OMIM:612530	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000219	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0002119	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000218	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000455	PMID:17873649	PCS		4/5			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0002558	PMID:17873649	PCS		2/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000776	PMID:17873649	PCS	HP:0003577	2/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0003422	OMIM:612530	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001762	PMID:17873649	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0002650	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001321	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0001360	OMIM:612530	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0005280	PMID:17873649	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0002007	PMID:17873649	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000268	PMID:17873649	PCS		1/7			P	HPO:probinson[2022-05-30];HPO:probinson[2022-05-30]
OMIM:612530	Chromosome 1q41-q42 deletion syndrome		HP:0000028	OMIM:612530	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602723	Psoriasis 2		HP:0001036	PMID:15689454	PCS					P	HPO:skoehler[2015-08-16];HPO:probinson[2020-10-13]
OMIM:602723	Psoriasis 2		HP:0040189	PMID:15689454	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-13]
OMIM:602723	Psoriasis 2		HP:0025092	PMID:15689454	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-13]
OMIM:602723	Psoriasis 2		HP:0003765	PMID:22521418	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-13]
OMIM:602723	Psoriasis 2		HP:0000006	PMID:22521418	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-13]
OMIM:602723	Psoriasis 2		HP:0000962	PMID:15689454	PCS					P	HPO:skoehler[2015-08-16];HPO:probinson[2020-10-13]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0003577	PMID:23704329	PCS		1/1			C	HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001058	PMID:23704329	PCS		1/1			P	HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000343	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000023	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000160	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0003196	OMIM:615539	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001075	PMID:23704329	PCS		1/1			P	HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000316	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000678	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000218	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000411	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001249	PMID:23704329	PCS		0/1			P	HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0003326	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000297	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001166	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0003324	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000494	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0002059	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001762	OMIM:615539	TAS				HP:0012832	P	HPO:skoehler[2013-11-28]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001382	PMID:23704329	PCS		1/1			P	HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0004474	PMID:23704329	PCS		1/1			P	HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000592	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0011800	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0002194	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001181	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0012385	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0002829	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000506	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000007	PMID:23704329	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0002007	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001653	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001634	OMIM:615539	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0000248	PMID:23704329;OMIM:615539	PCS		11/11			P	HPO:probinson[2023-01-25];HPO:skoehler[2013-11-28]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001655	PMID:23704329	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-25]
OMIM:615539	Ehlers-Danlos syndrome, musculocontractural type, 2		HP:0001776	PMID:23704329	PCS	HP:0003577	1/1			P	HPO:probinson[2023-01-25]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0002573	PMID:22476154	PCS	HP:0003593	1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0000155	PMID:22476154	PCS	HP:0003623	1/1			P	HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0004387	PMID:19890111	PCS	HP:0003593	1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0100280	PMID:22476154	PCS	HP:0003623	1/1			P	HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0002583	PMID:22476154	PCS		1/1			P	HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0000007	PMID:21519361	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0000999	PMID:22476154	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0009789	PMID:19890111	PCS	HP:0003593	1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0025084	PMID:21519361	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-10-09]
OMIM:613148	Inflammatory bowel disease 28, early onset, autosomal recessive		HP:0001510	PMID:22476154	PCS		1/1			P	HPO:probinson[2020-10-09]
OMIM:600652	Deafness, autosomal dominant nonsyndromic sensorineural 4		HP:0000408	OMIM:600652	IEA					P	HPO:iea[2009-02-17]
OMIM:600652	Deafness, autosomal dominant nonsyndromic sensorineural 4		HP:0000006	OMIM:600652	IEA					I	HPO:iea[2009-02-17]
OMIM:610441	Testicular microlithiasis		HP:0012215	PMID:16960801	TAS					P	HPO:probinson[2013-01-09]
OMIM:234700	Heart block, congenital		HP:0001685	OMIM:234700	IEA					P	HPO:iea[2009-02-17]
OMIM:234700	Heart block, congenital		HP:0006690	OMIM:234700	IEA					P	HPO:iea[2009-02-17]
OMIM:234700	Heart block, congenital		HP:0001692	OMIM:234700	PCS					P	HPO:probinson[2009-02-17]
OMIM:234700	Heart block, congenital		HP:0006681	OMIM:234700	IEA					P	HPO:iea[2009-02-17]
OMIM:234700	Heart block, congenital		HP:0000007	OMIM:234700	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:234700	Heart block, congenital		HP:0001638	OMIM:234700	IEA					P	HPO:iea[2009-02-17]
OMIM:234700	Heart block, congenital		HP:0001653	OMIM:234700	IEA					P	HPO:iea[2009-02-17]
OMIM:234700	Heart block, congenital		HP:0001678	OMIM:234700	IEA					P	HPO:iea[2009-02-17]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0001561	PMID:27543974	PCS	HP:0011461	3/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0001321	PMID:27543974	PCS		4/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0001272	PMID:27543974	PCS		2/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0001284	PMID:27543974	PCS		1/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0010851	PMID:27543974	PCS		1/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0011344	PMID:27543974	PCS		4/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0012110	PMID:27543974	PCS		4/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0006380	PMID:27543974	PCS		1/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0007141	PMID:27543974	PCS		2/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0000007	PMID:27543974	PCS					I	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0000648	PMID:27543974	PCS		2/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0001319	PMID:27543974	PCS	HP:0003623				P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0001522	PMID:27543974	PCS		4/4			C	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0002987	PMID:27543974	PCS		1/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0004887	PMID:27543974	PCS	HP:0003623	4/4			P	HPO:probinson[2021-07-06]
OMIM:619303	Pontocerebellar hypoplasia, type 1E		HP:0001336	PMID:27543974	PCS		2/4			P	HPO:probinson[2021-07-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0000054	PMID:25192046	PCS		3/3	MALE		P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0003621	PMID:25192046	PCS		1/4			C	HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0030344	PMID:25192046	PCS		4/4			P	HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0030341	PMID:25192046	PCS		4/4			P	HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0040171	PMID:25192046	PCS		2/2	MALE		P	HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0011463	PMID:25192046	PCS		3/4			C	HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0000458	PMID:25192046	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0000007	PMID:25192046	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0008214	PMID:25192046	PCS		1/1	FEMALE		P	HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0008734	PMID:25192046	PCS		3/3	MALE		P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0000135	PMID:25192046	PCS		4/4			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0020159	PMID:25192046	PCS		1/1			P	HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0000028	PMID:25192046	PCS		3/3	MALE		P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-06]
OMIM:616030	Hypogonadotropic hypogonadism 22 with or without anosmia		HP:0000786	PMID:25192046	PCS		1/1	FEMALE		P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-06]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003236	PMID:33239111	PCS		5/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003596	PMID:33239111	PCS		3/7			C	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003693	PMID:33239111	PCS		3/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003593	PMID:33239111	PCS		1/7			C	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0001251	PMID:33239111	PCS		3/6			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000580	PMID:33239111	PCS		2/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003690	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0030319	PMID:33239111	PCS		5/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0100297	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000616	PMID:33239111	PCS		1/6			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0011462	PMID:33239111	PCS		3/7			C	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000613	PMID:33239111	PCS		1/6			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003805	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003700	PMID:33239111	PCS		2/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0001265	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0002015	PMID:33239111	PCS		5/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0001260	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09];HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0002352	PMID:33239111	PCS		3/6			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0031237	PMID:33239111	PCS		1/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000407	PMID:33239111	PCS		1/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000508	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000602	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0002922	PMID:33239111	PCS		5/5			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000405	PMID:33239111	PCS		1/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000006	PMID:33239111	PCS					I	HPO:probinson[2021-10-09];HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0001337	PMID:33239111	PCS		1/6			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0000467	PMID:33239111	PCS		3/7			P	HPO:probinson[2021-10-09]
OMIM:619473	Oculopharyngodistal myopathy 3		HP:0003557	PMID:33239111	PCS		7/7			P	HPO:probinson[2021-10-09]
OMIM:616740	Immunodeficiency 46		HP:0005425	PMID:26642240	PCS		11/14			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0001287	PMID:26642240	PCS		2/14			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0004313	PMID:26642240	PCS					P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0009098	PMID:26642240	IEA		1/14			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0001508	PMID:26642240	PCS		4/14			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0001903	PMID:26642240	PCS		2/4		HP:0012825	P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0000509	PMID:26642240	PCS		3/14			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0100806	PMID:26642240	PCS		5/14			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0000007	PMID:26642240	PCS					I	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0002028	PMID:26642240	PCS		10/14			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0004854	PMID:26642240	PCS		4/4			P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0001875	PMID:26642240	PCS					P	HPO:probinson[2017-06-17]
OMIM:616740	Immunodeficiency 46		HP:0002721	OMIM:616740	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0002465	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0002421	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0003236	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0003577	OMIM:615249	TAS					C	HPO:skoehler[2015-12-30]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0002365	OMIM:615249	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001250	OMIM:615249	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001371	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001274	OMIM:615249	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0031882	OMIM:615249	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001090	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0007260	PMID:24925318	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-23]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000518	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0007663	OMIM:615249	TAS					P	HPO:skoehler[2015-07-26]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000238	PMID:24925318	PCS		1/1			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-23]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000253	OMIM:615249	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000252	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0002650	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001321	OMIM:615249	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0011968	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001263	OMIM:615249	TAS				HP:0012828	P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0003560	PMID:24925318	PCS		1/1			P	HPO:skoehler[2014-07-11];HPO:probinson[2023-01-23]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0011344	PMID:24925318	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0034197	PMID:24925318	PCS		1/1			C	HPO:probinson[2023-01-23]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000407	OMIM:615249	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0032792	PMID:24925318	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001339	OMIM:615249	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000546	PMID:24925318	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-23]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000568	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000007	OMIM:615249	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000505	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0001319	OMIM:615249	TAS					P	HPO:skoehler[2015-01-04]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0002747	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615249	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12		HP:0000589	OMIM:615249	TAS					P	HPO:skoehler[2014-07-11]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0001397	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0002155	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0003124	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0004322	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0002240	OMIM:612526	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0003593	OMIM:612526	IEA					C	HPO:skoehler[2019-04-18]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0000819	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0009064	OMIM:612526	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0000855	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0000007	PMID:18211975	PCS					I	HPO:probinson[2013-01-09]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0009125	OMIM:612526	IEA					P	HPO:skoehler[2015-01-27]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0000956	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0003758	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0002901	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0001433	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0001007	PMID:18211975	PCS					P	HPO:probinson[2013-03-12]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0001744	OMIM:612526	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612526	Lipodystrophy, congenital generalized, type 3		HP:0000786	OMIM:612526	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0002014	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000252	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000340	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000494	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000486	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000750	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0002013	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0011968	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0001250	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0001263	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0003186	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000609	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000639	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0007099	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0001548	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000648	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0002119	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0100716	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0002007	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0000256	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0002019	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:613638	Chromosome 19p13.13 deletion syndrome		HP:0002027	PMID:20613546	PCS					P	HPO:probinson[2017-06-23]
OMIM:258800	Oral sensibility, disturbance of		HP:0002311	OMIM:258800	TAS					P	HPO:probinson[2009-02-17]
OMIM:258800	Oral sensibility, disturbance of		HP:0000007	OMIM:258800	TAS					I	HPO:probinson[2009-02-17]
OMIM:258800	Oral sensibility, disturbance of		HP:0002307	OMIM:258800	TAS					P	HPO:probinson[2009-02-17]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0004754	PMID:23264583;PMID:19343045	PCS		9/19			P	HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0003596	PMID:16772329	PCS		2/3			C	HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0025708	PMID:23264583	PCS		2/2			C	HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0005184	PMID:23264583	PCS		1/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0025710	PMID:16772329	PCS		1/3			C	HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0001962	PMID:16772329;PMID:19343045	PCS		29/31			P	HPO:probinson[2013-04-04];HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0004757	PMID:16772329;PMID:23264583;PMID:19343045	PCS		12/22			P	HPO:probinson[2013-01-09];HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0006699	PMID:19343045	PCS		16/20			P	HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0000006	PMID:16772329	PCS					I	HPO:probinson[2013-04-04]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0012248	PMID:23264583	PCS		1/2			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-07-10]
OMIM:612240	Atrial fibrillation, familial, 7		HP:0001688	PMID:19343045	PCS		3/21			P	HPO:probinson[2022-07-10]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0000154	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0010959	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0000252	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0004322	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0002164	OMIM:113477	PCS					P	HPO:probinson[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0004220	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0001999	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0000307	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0000006	OMIM:113477	IEA					I	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0000445	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0004227	OMIM:113477	IEA					P	HPO:iea[2009-02-17]
OMIM:113477	Brachymorphism-Onychodysplasia-Dysphalangism syndrome		HP:0001798	OMIM:113477	PCS					P	HPO:probinson[2012-03-03]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0000121	OMIM:616026	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0001520	PMID:22802087	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0004322	OMIM:616026	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0003355	OMIM:616026	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0003155	PMID:22802087	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0002240	PMID:22802087	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0003076	PMID:22802087	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0000093	PMID:22802087	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0000819	OMIM:616026	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0002748	PMID:22802087	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0001943	PMID:22802087	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0003109	OMIM:616026	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0003537	OMIM:616026	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0002910	PMID:22802087	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0001942	PMID:22802087	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0002148	PMID:22802087	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0000006	PMID:22802087	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616026	Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young		HP:0003623	PMID:22802087	PCS		1/1			C	HPO:probinson[2022-03-26]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0002069	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001276	PMID:33220177	PCS		5/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0002510	PMID:33220177	PCS		8/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0002188	PMID:33220177	PCS		2/8			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001344	PMID:33220177	PCS		8/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001321	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0002365	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001332	PMID:33220177	PCS		3/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001274	PMID:33220177	PCS		8/8			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001252	PMID:33220177	PCS		6/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0410252	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0032794	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001270	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0012434	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0012469	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0012110	PMID:33220177	PCS		9/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0000007	PMID:33220177	PCS					I	HPO:probinson[2021-06-02];HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0000238	PMID:33220177	PCS		0/8			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001522	PMID:33220177	PCS		3/9			C	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0007359	PMID:33220177	PCS		2/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001873	PMID:33220177	PCS		2/9		HP:0011010	P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0001348	PMID:33220177	PCS		8/9			P	HPO:probinson[2021-06-02]
OMIM:619301	Pontocerebellar hypoplasia, type 14		HP:0009879	PMID:33220177	PCS		5/8			P	HPO:probinson[2021-06-02]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0003774	PMID:24676636	PCS	HP:0003581	6/6			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0003621	PMID:24676636	PCS		1/5			C	HPO:probinson[2022-11-07]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0000100	PMID:24676636	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0003584	PMID:24676636	PCS		1/5			C	HPO:probinson[2022-11-07]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0000097	PMID:24676636	PCS		9/9			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0011462	PMID:24676636	PCS		3/5			C	HPO:probinson[2022-11-07]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0000093	PMID:24676636	PCS		5/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-07]
OMIM:616032	Focal segmental glomerulosclerosis 8		HP:0000006	PMID:24676636	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-07]
OMIM:108725	Atherosclerosis susceptibility		HP:0002155	OMIM:108725	TAS					P	HPO:probinson[2009-02-17]
OMIM:108725	Atherosclerosis susceptibility		HP:0003233	OMIM:108725	TAS					P	HPO:probinson[2012-10-20]
OMIM:108725	Atherosclerosis susceptibility		HP:0001658	OMIM:108725	TAS					P	HPO:probinson[2009-02-17]
OMIM:108725	Atherosclerosis susceptibility		HP:0000006	OMIM:108725	IEA					I	HPO:iea[2009-02-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0000286	PMID:18628315	PCS		15/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002465	OMIM:610443	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610443	Koolen-De Vries syndrome		HP:0005656	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001212	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000486	PMID:18628315	PCS		10/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0004322	PMID:18628315	PCS		4/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002021	PMID:20301783	PCS		HP:0040283			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001250	PMID:18628315	PCS		11/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001290	PMID:18628315	PCS	HP:0011463	21/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0004283	PMID:18628315	PCS		5/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000518	PMID:18628315	PCS		1/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000958	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0001647	PMID:20301783	PCS		HP:0040283			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002616	PMID:19447831	PCS		1/11			P	HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000752	OMIM:610443	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610443	Koolen-De Vries syndrome		HP:0001643	PMID:18628315	PCS	HP:0003577	1/22			P	HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001642	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0001249	OMIM:610443	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610443	Koolen-De Vries syndrome		HP:0001601	OMIM:610443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610443	Koolen-De Vries syndrome		HP:0000175	PMID:18628315	PCS		2/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001385	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000252	PMID:18628315	PCS		1/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000010	PMID:20301783	PCS		HP:0040284			P	HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002079	OMIM:610443	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610443	Koolen-De Vries syndrome		HP:0001382	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0010719	PMID:18628315	PCS		13/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001263	PMID:18628315	PCS		22/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0100024	PMID:18628315	PCS		16/18			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002827	PMID:18628315	PCS		6/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002948	PMID:20301783	PCS		HP:0040283			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000767	PMID:18628315	PCS		5/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000964	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0000601	PMID:20301783	PCS		HP:0040283			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000447	PMID:18628315	PCS		18/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000400	PMID:18628315	PCS		13/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000960	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0000006	PMID:19447831	PCS					I	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000204	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0000126	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0001611	PMID:18628315	PCS		6/12			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000687	PMID:19447831;OMIM:610443	PCS		14/21			P	HPO:skoehler[2013-01-22];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000582	PMID:18628315	PCS		15/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000189	PMID:18628315	PCS		11/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000540	PMID:18628315	PCS		8/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002286	PMID:20301783	PCS		HP:0040283			P	HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000581	PMID:18628315	PCS		8/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002282	OMIM:610443	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610443	Koolen-De Vries syndrome		HP:0040080	PMID:19447831	PCS		4/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001508	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0001629	PMID:19447831	PCS		1/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000739	PMID:20301783	PCS		HP:0040283			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000337	PMID:18628315	PCS		15/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000414	PMID:18628315	PCS		20/21			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0008872	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002119	PMID:18628315	PCS		6/16			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000218	PMID:18628315	PCS		11/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0006610	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0001466	PMID:20301783	PCS					I	HPO:skoehler[2013-01-22];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000396	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0003302	PMID:20301783	PCS		HP:0040283			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000076	PMID:19447831	PCS		2/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000750	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002650	PMID:18628315	PCS		8/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000232	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000276	PMID:18628315	PCS		14/22			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000194	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0005487	PMID:18628315	PCS		1/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0002011	PMID:20301783	PCS		HP:0040282			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0011822	PMID:18628315	PCS		9/22			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0100710	OMIM:610443	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610443	Koolen-De Vries syndrome		HP:0002808	PMID:18628315	PCS		8/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001518	PMID:18628315	PCS		6/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000508	PMID:18628315	PCS		11/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000426	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0000348	PMID:18628315	PCS		15/22			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0007730	PMID:18628315	PCS		10/22			P	HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001511	OMIM:610443	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610443	Koolen-De Vries syndrome		HP:0001631	PMID:19447831	PCS	HP:0003577	2/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0006006	PMID:18628315	PCS		5/18			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0000028	PMID:18628315	PCS		7/9	MALE		P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:610443	Koolen-De Vries syndrome		HP:0001238	PMID:18628315	PCS		11/18			P	HPO:iea[2010-09-08];HPO:probinson[2020-08-02]
OMIM:155350	MEGALENCEPHALY		HP:0001355	PMID:7274594	PCS		HP:0040280			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-02];HP:probinson[2019-01-03]
OMIM:155350	MEGALENCEPHALY		HP:0000238	PMID:4855950	PCS		2/10			P	HPO:lccarmody[2018-10-02];HPO:lccarmody[2018-10-02]
OMIM:155350	MEGALENCEPHALY		HP:0000256	PMID:7274594	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:155350	MEGALENCEPHALY		HP:0000006	PMID:7274594	PCS					I	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-02]
OMIM:155350	MEGALENCEPHALY		HP:0001249	PMID:7274594	PCS		7/109			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-02]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000341	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000154	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000750	PMID:30879640	PCS		4/4			P	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0031936	PMID:30879640	PCS		4/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0002032	PMID:30879640	PCS	HP:0003577	1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0005487	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000193	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0001274	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0001263	PMID:30879640	PCS		5/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0001252	PMID:30879640	PCS		3/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0002162	PMID:30879640	PCS		2/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000185	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0009909	PMID:30879640	PCS		2/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0005280	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000316	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0008872	PMID:30879640	PCS		5/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000414	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000218	PMID:30879640	PCS		2/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0002714	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0200055	PMID:30879640	PCS		3/5			P	HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0002007	PMID:30879640	PCS		1/5			P	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0000006	PMID:30879640	PCS					I	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618779	Coffin-Siris syndrome 11		HP:0001249	PMID:30879640	PCS		4/4			P	HPO:probinson[2020-05-10]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000343	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000486	PMID:34102099	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0001250	PMID:34102099	PCS		3/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000262	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0001252	PMID:34102099	PCS		6/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0012803	PMID:34102099	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0009381	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000716	PMID:34102099	PCS		1/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0011220	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000718	PMID:34102099	PCS		4/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000739	PMID:34102099	PCS		1/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0002938	PMID:34102099	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000752	PMID:34102099	PCS		3/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0001763	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0001249	PMID:34102099	PCS		8/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0030820	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000750	PMID:34102099	PCS		8/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0001263	PMID:34102099	PCS		8/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0004691	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000729	PMID:34102099	PCS		3/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000646	PMID:34102099	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000722	PMID:34102099	PCS		1/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0100716	PMID:34102099	PCS		1/8			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000768	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23];HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0004209	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0002007	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000565	PMID:34102099	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0002942	PMID:34102099	PCS		1/6			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0001257	PMID:34102099	PCS		1/7			P	HPO:probinson[2022-01-23]
OMIM:619467	Usmani-Riazuddin syndrome, autosomal dominant		HP:0000006	PMID:34102099	PCS					I	HPO:probinson[2022-01-23]
OMIM:601228	Polyposis syndrome, hereditary mixed, 1		HP:0001438	OMIM:601228	IEA					P	HPO:iea[2009-02-17]
OMIM:601228	Polyposis syndrome, hereditary mixed, 1		HP:0000006	OMIM:601228	IEA					I	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000164	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0003016	PMID:30773277	PCS		4/9			P	HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0001377	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0008905	PMID:30773277	PCS		3/9			P	HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000463	OMIM:271510	TAS					P	HPO:probinson[2013-04-09]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0004586	PMID:30773277	PCS		5/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0001156	PMID:30773277	PCS		3/9			P	HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0003196	OMIM:271510	TAS					P	HPO:probinson[2013-04-09]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0003370	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0004482	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0031367	OMIM:271510	IEA		7/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0010585	PMID:30773277	PCS		2/9			P	HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0001607	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0008450	PMID:30773277	PCS		1/9			P	HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000938	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002938	OMIM:271510	TAS					P	HPO:probinson[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0008873	PMID:30773277	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000316	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000414	OMIM:271510	IEA					P	HPO:skoehler[2019-09-07]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002812	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002857	PMID:30773277	PCS		3/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000851	OMIM:271510	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0007787	OMIM:271510	IEA					P	HPO:skoehler[2010-06-20]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0008755	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0006336	OMIM:271510	TAS					P	HPO:skoehler[2012-10-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0001249	OMIM:271510	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0004315	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002751	PMID:30773277	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0003027	PMID:30773277	PCS		1/9			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002750	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002970	OMIM:271510	IEA					P	HPO:skoehler[2019-09-07]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0003025	PMID:30773277	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002651	PMID:30773277	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000272	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0011800	OMIM:271510	TAS					P	HPO:skoehler[2013-11-28]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0005280	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0008486	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000926	PMID:30773277	PCS		8/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002308	OMIM:271510	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000007	PMID:30773277	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-23]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002007	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0002942	OMIM:271510	IEA					P	HPO:iea[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0001216	OMIM:271510	TAS					P	HPO:probinson[2009-02-17]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0000303	OMIM:271510	IEA					P	HPO:skoehler[2019-09-07]
OMIM:271510	Spondyloepimetaphyseal dysplasia, sponastrime type		HP:0001875	OMIM:271510	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000286	PMID:17704777	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0003577	PMID:17704777	PCS		5/5			C	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000365	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0001156	PMID:17704777	PCS		1/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0004322	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000463	PMID:17704777	PCS		3/5			P	HPO:probinson[2022-10-20];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0001252	PMID:17704777	PCS		3/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0003196	PMID:17704777	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000162	PMID:17704777	PCS		1/5			P	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0002020	PMID:17704777	PCS		4/5			P	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0012745	PMID:17704777	PCS		2/5			P	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0012368	PMID:17704777	PCS		3/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000717	PMID:17704777	PCS		0/5			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-14]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000316	PMID:17704777	PCS		1/5			P	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000954	PMID:17704777	PCS		3/5			P	HPO:probinson[2022-10-20];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000414	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000219	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0030084	OMIM:613604	TAS					P	HPO:skoehler[2014-09-21]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000218	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0003745	PMID:17704777	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-14]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0001249	PMID:17704777	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000358	PMID:17704777	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000494	PMID:17704777	PCS		3/5			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000431	PMID:17704777	PCS		2/5			P	HPO:probinson[2022-10-20];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000276	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0011968	PMID:17704777	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000194	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000490	PMID:17704777	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0001263	PMID:17704777	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0045025	PMID:17704777	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-14]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0012385	PMID:17704777	PCS		2/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000348	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000601	PMID:17704777	PCS		2/5			P	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000403	PMID:17704777	PCS		4/5			P	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0002007	PMID:17704777	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0001511	PMID:17704777	PCS		0/5			P	HPO:skoehler[2012-12-03];HPO:probinson[2024-03-14]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0001510	PMID:17704777	PCS		2/5			P	HPO:skoehler[2012-11-28];HPO:probinson[2024-03-14]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000201	PMID:17704777	PCS		1/5			P	HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000369	PMID:17704777	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:613604	Chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-mb		HP:0000347	PMID:17704777	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-20]
OMIM:618751	Spermatogenic failure 43		HP:0032560	PMID:31278745	PCS			MALE		P	HPO:probinson[2020-04-29]
OMIM:618751	Spermatogenic failure 43		HP:0003251	PMID:31151990	PCS			MALE		P	HPO:probinson[2020-04-29]
OMIM:618751	Spermatogenic failure 43		HP:0000007	PMID:31151990	PCS					I	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:618751	Spermatogenic failure 43		HP:0012207	PMID:31278745	PCS			MALE		P	HPO:probinson[2020-04-29]
OMIM:618751	Spermatogenic failure 43		HP:0033525	PMID:31048344;PMID:31278745	PCS		3/3			P	HPO:probinson[2021-02-13]
OMIM:618751	Spermatogenic failure 43		HP:0032558	PMID:31151990	PCS			MALE		P	HPO:probinson[2020-04-29]
OMIM:607671	Dystonia 13, torsion		HP:0000473	OMIM:607671	IEA					P	HPO:iea[2009-02-17]
OMIM:607671	Dystonia 13, torsion		HP:0002356	OMIM:607671	IEA					P	HPO:iea[2009-02-17]
OMIM:607671	Dystonia 13, torsion		HP:0002451	OMIM:607671	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607671	Dystonia 13, torsion		HP:0012048	OMIM:607671	IEA					P	HPO:iea[2009-02-17]
OMIM:607671	Dystonia 13, torsion		HP:0000006	OMIM:607671	IEA					I	HPO:iea[2009-02-17]
OMIM:607671	Dystonia 13, torsion		HP:0001304	OMIM:607671	IEA					P	HPO:iea[2009-02-17]
OMIM:607671	Dystonia 13, torsion		HP:0001337	OMIM:607671	IEA					P	HPO:iea[2009-02-17]
OMIM:607671	Dystonia 13, torsion		HP:0000643	OMIM:607671	IEA					P	HPO:iea[2009-02-17]
OMIM:608542	Aneurysm, intracranial berry, 2		HP:0007029	OMIM:608542	TAS					P	HPO:probinson[2017-06-21]
OMIM:608542	Aneurysm, intracranial berry, 2		HP:0002138	OMIM:608542	TAS					P	HPO:probinson[2017-06-21]
OMIM:601200	Pleuropulmonary blastoma		HP:0100528	PMID:21266384	PCS	HP:0011463	11/14			P	HPO:skoehler[2012-10-17];HP:probinson[2018-09-16]
OMIM:601200	Pleuropulmonary blastoma		HP:0002859	PMID:19556464	PCS					P	HPO:skoehler[2012-10-17];HP:probinson[2018-09-16]
OMIM:601200	Pleuropulmonary blastoma		HP:0000006	OMIM:601200;PMID:19556464	TAS		20/20			I	HPO:skoehler[2012-10-17];HP:probinson[2018-09-16];HP:probinson[2018-09-16]
OMIM:601200	Pleuropulmonary blastoma		HP:0002885	PMID:21266384	TAS		1/86			P	HPO:skoehler[2012-10-17];HP:probinson[2018-09-16]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0005313	PMID:32938213	PCS		4/4			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0010648	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000460	PMID:32938213	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0001075	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0033982	PMID:32938213	PCS		2/4			P	HPO:probinson[2021-07-16]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0004938	PMID:32938213	PCS		3/4			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0004937	PMID:32938213	PCS		1/4			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000678	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000977	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000218	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0001027	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0001763	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000974	PMID:32938213	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0002036	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000494	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0005302	PMID:32938213	PCS		2/4			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0002650	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0001382	PMID:32938213	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0002076	PMID:32938213	PCS		5/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000490	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0001065	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000592	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000272	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0100858	PMID:32938213	PCS		1/4			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0032153	PMID:32938213	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0033981	PMID:32938213	PCS		4/4			P	HPO:probinson[2021-07-16]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000767	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0003835	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000268	PMID:32938213	PCS		2/6			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0004944	PMID:32938213	PCS		1/4			P	HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000006	PMID:32938213	PCS					I	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619329	Fibromuscular dysplasia, multifocal		HP:0000347	PMID:32938213	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:608224	Deafness, autosomal dominant 41		HP:0003621	PMID:23345450	PCS					C	HPO:probinson[2023-04-22]
OMIM:608224	Deafness, autosomal dominant 41		HP:0025708	PMID:23345450	PCS					C	HPO:probinson[2023-04-22]
OMIM:608224	Deafness, autosomal dominant 41		HP:0000408	PMID:23345450	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-22]
OMIM:608224	Deafness, autosomal dominant 41		HP:0000360	PMID:23345450	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-22]
OMIM:608224	Deafness, autosomal dominant 41		HP:0000006	PMID:23345450	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-22]
OMIM:617304	Retinitis pigmentosa 77		HP:0001133	PMID:27889058	PCS		3/5			P	HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0003621	PMID:27889058	PCS		3/5			C	HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0007737	PMID:27889058	PCS		3/5			P	HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0000662	PMID:27889058	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0011505	PMID:27889058	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0025708	PMID:27889058	PCS		1/5			C	HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0011463	PMID:27889058	PCS		1/5			C	HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0000007	PMID:27889058	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0007663	PMID:27889058	PCS		5/5		HP:0003676	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0007787	PMID:27889058	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0000510	PMID:27889058	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0007843	PMID:27889058	PCS		5/5			P	HPO:probinson[2023-02-10]
OMIM:617304	Retinitis pigmentosa 77		HP:0001105	PMID:27889058	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:119600	Cleidocranial dysplasia		HP:0008848	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000242	PMID:20931042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-03]
OMIM:119600	Cleidocranial dysplasia		HP:0005259	PMID:20931042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-03]
OMIM:119600	Cleidocranial dysplasia		HP:0000365	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000882	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0004322	PMID:28878609	PCS		2/3			P	HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0003396	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:6000872	PMID:16463420	PCS					P	HPO:probinson[2024-08-03]
OMIM:119600	Cleidocranial dysplasia		HP:0000680	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:6000875	PMID:20931042	PCS					P	HPO:probinson[2024-08-03]
OMIM:119600	Cleidocranial dysplasia		HP:0000316	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000239	PMID:28878609	PCS		2/3			P	HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0002738	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002812	PMID:28878609	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0002659	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0003304	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000891	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000175	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0011800	OMIM:119600	TAS					P	HPO:skoehler[2013-11-28]
OMIM:119600	Cleidocranial dysplasia		HP:0002827	PMID:28878609	PCS		1/3			P	HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0006660	PMID:28878609	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0009577	OMIM:119600	TAS					P	HPO:probinson[2013-12-15]
OMIM:119600	Cleidocranial dysplasia		HP:0002705	OMIM:119600	TAS					P	HPO:skoehler[2015-12-30]
OMIM:119600	Cleidocranial dysplasia		HP:0002700	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002866	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000006	PMID:9182765	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0003577	PMID:28878609	PCS		3/3			C	HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0000189	OMIM:119600	TAS					P	HPO:iea[2013-08-11]
OMIM:119600	Cleidocranial dysplasia		HP:0001156	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002684	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0004220	OMIM:119600	TAS					P	HPO:probinson[2013-12-15]
OMIM:119600	Cleidocranial dysplasia		HP:0100864	OMIM:119600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:119600	Cleidocranial dysplasia		HP:0011001	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0010230	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0006297	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000218	OMIM:119600	TAS					P	HPO:iea[2013-08-11]
OMIM:119600	Cleidocranial dysplasia		HP:0000774	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000696	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000894	PMID:28878609	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0000773	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0003302	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002650	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000431	PMID:28878609	PCS		1/3			P	HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0002098	OMIM:119600	IEA					P	HPO:skoehler[2019-09-07]
OMIM:119600	Cleidocranial dysplasia		HP:0004474	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000272	PMID:28878609	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0003183	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0011069	PMID:28878609	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:119600	Cleidocranial dysplasia		HP:0005280	PMID:20931042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-03]
OMIM:119600	Cleidocranial dysplasia		HP:0006040	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002808	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002689	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002007	PMID:20931042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-03]
OMIM:119600	Cleidocranial dysplasia		HP:0002645	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0008788	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0000347	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:119600	Cleidocranial dysplasia		HP:0002643	OMIM:119600	TAS					P	HPO:probinson[2013-12-15]
OMIM:119600	Cleidocranial dysplasia		HP:0002688	OMIM:119600	IEA					P	HPO:iea[2009-02-17]
OMIM:154700	Marfan syndrome		HP:0430043	PMID:31772430	PCS		16/21			P	HPO:probinson[2024-08-04];HPO:probinson[2024-08-04]
OMIM:154700	Marfan syndrome		HP:0000483	PMID:33436942	PCS		3/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001377	PMID:28050285;PMID:33436942	PCS		29/199			P	HPO:probinson[2021-05-27];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000486	PMID:8172269	PCS		110/573			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-08-03]
OMIM:154700	Marfan syndrome		HP:0005136	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0001371	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0003199	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0025586	PMID:8172269	PCS		8/573			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0000518	PMID:33436942;PMID:26903188	PCS		118/199			P	HPO:probinson[2012-04-24];HP:probinson[2018-09-03];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0008132	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0002816	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0002616	PMID:33436942	PCS		45/58			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001647	PMID:33436942	PCS		1/58			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000678	PMID:33436942	PCS		8/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0008138	PMID:28050285	PCS		31/146			P	HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0001840	PMID:33436942	PCS		7/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001763	PMID:33436942	PCS		27/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000278	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0007800	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0001765	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0002751	PMID:28050285	PCS		37/146			P	HPO:probinson[2012-04-24];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0000494	PMID:33436942	PCS		19/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000098	OMIM:154700	TAS					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0004970	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0001382	PMID:33436942	PCS		11/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0003088	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0000490	PMID:33436942;OMIM:154700	PCS		25/63			P	HPO:probinson[2021-04-01];HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0001065	PMID:33436942	PCS		11/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0005180	PMID:33436942	PCS		26/58			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0012385	PMID:33436942	PCS		19/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0100775	PMID:10489951;PMID:3189335	PCS		112/140			P	HPO:probinson[2020-08-03];HPO:skoehler[2013-01-22];HPO:probinson[2020-08-03]
OMIM:154700	Marfan syndrome		HP:0000767	PMID:28050285	PCS		44/146			P	HPO:probinson[2012-04-24];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0004927	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0003758	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0001659	PMID:33436942	PCS		14/58			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0007676	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0000768	PMID:28050285	PCS		58/146			P	HPO:probinson[2012-04-24];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0000565	PMID:8172269	PCS		12/573			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-08-03]
OMIM:154700	Marfan syndrome		HP:0001653	PMID:33436942	PCS		33/58			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0002107	PMID:33436942	PCS		6/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000006	PMID:17502658	PCS					I	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0032934	PMID:8530937	PCS	HP:0011462	HP:0040284			P	HPO:probinson[2020-08-03]
OMIM:154700	Marfan syndrome		HP:0000189	OMIM:154700	TAS					P	HPO:skoehler[2013-08-18]
OMIM:154700	Marfan syndrome		HP:0000541	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0003179	PMID:28050285;PMID:26339165	PCS		140/292			P	HPO:probinson[2012-04-24];HP:probinson[2018-09-03];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0012773	PMID:28050285	PCS		54/146			P	HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0001704	PMID:33436942	PCS		31/58			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000218	PMID:33436942	PCS		34/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001786	PMID:33436942	PCS		33/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000577	PMID:8172269;PMID:33436942	PCS		72/626			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-08-03];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001166	PMID:28050285;PMID:33436942	PCS		124/197			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0000275	OMIM:154700	TAS					P	HPO:probinson[2012-05-01]
OMIM:154700	Marfan syndrome		HP:0003302	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0002650	PMID:33436942	PCS		16/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001883	PMID:33436942	PCS		13/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0004872	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0000276	OMIM:154700	TAS					P	HPO:probinson[2012-05-01]
OMIM:154700	Marfan syndrome		HP:0030961	PMID:33436942	PCS		2/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001761	PMID:28050285	PCS		49/146			P	HPO:probinson[2012-04-24];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0025599	PMID:8172269	PCS		3/573			P	HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0002097	OMIM:154700	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0000272	PMID:33436942	PCS		31/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001083	PMID:28050285;PMID:29587526;PMID:33436942	PCS		119/251			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0001519	PMID:33436942	PCS		38/53			P	HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0001635	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0002647	PMID:33436942	PCS		1/58			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000268	PMID:33436942	PCS		36/53			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01]
OMIM:154700	Marfan syndrome		HP:0000501	PMID:1494814;PMID:29587526	PCS		29/625			P	HPO:skoehler[2013-01-22];HPO:probinson[2021-05-27];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0000347	OMIM:154700	IEA					P	HPO:probinson[2012-04-24]
OMIM:154700	Marfan syndrome		HP:0001634	PMID:2791251;PMID:33436942	PCS		67/111			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01];HPO:probinson[2021-05-27]
OMIM:154700	Marfan syndrome		HP:0000545	PMID:28050285;PMID:29587526;PMID:33436942	PCS		93/251			P	HPO:probinson[2012-04-24];HPO:probinson[2021-04-01];HPO:probinson[2021-05-27]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0006989	PMID:24482476	PCS		2/8			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0000486	PMID:24482476	PCS		1/10			P	HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001371	OMIM:613162	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0003593	PMID:28327087	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0002064	PMID:28327087	PCS		1/1			P	HPO:skoehler[2010-06-19]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0002061	PMID:28327087	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001270	PMID:28327087	PCS		2/2			P	HPO:skoehler[2010-06-19]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0033725	PMID:28327087	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0000639	OMIM:613162	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0011463	PMID:24482476	PCS		2/10			C	HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0011462	PMID:24482476	PCS		4/10			C	HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001249	PMID:24482476;PMID:28327087	PCS		5/12			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:skoehler[2010-06-19];HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001347	PMID:24482476	PCS		10/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0008936	PMID:28327087	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0003202	PMID:24482476	PCS		8/10			P	HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0002059	PMID:28327087	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0003621	PMID:24482476	PCS		4/10			C	HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0000750	PMID:28327087	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001762	PMID:28327087	PCS		2/2			P	HPO:skoehler[2014-03-24]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0003487	PMID:24482476	PCS		10/10			P	HPO:skoehler[2010-06-19]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0002079	PMID:24482476	PCS		5/8			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001260	PMID:28327087	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001263	PMID:28327087	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0011448	PMID:28327087	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0000007	PMID:24482476	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0000648	OMIM:613162	IEA		1/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0030051	PMID:28327087	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0001258	PMID:24482476	PCS		9/9			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-12]
OMIM:613162	Spastic paraplegia 45, autosomal recessive		HP:0000545	OMIM:613162	IEA					P	HPO:skoehler[2010-06-20]
OMIM:615513	Immunodeficiency 14		HP:0005425	PMID:24165795	PCS	HP:0011463				P	HPO:skoehler[2014-06-24];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0005403	PMID:24136356	PCS		12/17			P	HP:probinson[2019-01-20];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0030388	PMID:24136356	PCS		8/16			P	HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0002110	PMID:24136356	PCS		12/16			P	HPO:skoehler[2014-06-24];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0003496	PMID:24136356	PCS		14/17			P	HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0012476	PMID:24136356	PCS		10/10			P	HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0100658	PMID:24136356	PCS					P	HPO:skoehler[2014-06-24];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0002716	PMID:24165795	PCS		5/7			P	HPO:skoehler[2014-06-24];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0030381	PMID:24136356	PCS		14/16			P	HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0002205	PMID:24136356	PCS		17/17			P	HPO:skoehler[2014-06-24];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0008348	PMID:24136356	PCS		10/11			P	HP:probinson[2019-01-20];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0001744	PMID:24136356	PCS		10/17			P	HPO:skoehler[2014-06-24];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0000006	PMID:24136356	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0002721	PMID:24165795	PCS					P	HPO:skoehler[2015-01-27];HP:probinson[2019-01-20]
OMIM:615513	Immunodeficiency 14		HP:0410018	PMID:24136356	PCS		17/17			P	HPO:skoehler[2017-07-13];HP:probinson[2019-01-20]
OMIM:614619	Hyperekplexia 2		HP:0001276	PMID:11929858	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0002036	PMID:11929858	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0002267	PMID:11929858	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0010519	PMID:21391991	PCS	HP:0011461	9/9			P	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0000483	PMID:21391991	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0003577	PMID:21391991	PCS		9/9			C	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0003552	PMID:21391991	PCS	HP:0003577	9/9			P	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0002020	PMID:11929858	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0001270	PMID:11929858	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0030904	PMID:21391991	PCS		2/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0000007	PMID:11929858	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0000565	PMID:21391991	PCS		7/9			P	HPO:probinson[2013-08-10];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0000545	PMID:21391991	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0001249	PMID:21391991	PCS		1/9			P	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0003623	PMID:11929858	PCS		1/1			C	HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0001336	PMID:11929858	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-17]
OMIM:614619	Hyperekplexia 2		HP:0001347	PMID:11929858	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-17]
OMIM:267400	Renal, genital, and middle ear anomalies		HP:0000365	OMIM:267400	IEA					P	HPO:iea[2009-02-17]
OMIM:267400	Renal, genital, and middle ear anomalies		HP:0004452	OMIM:267400	IEA					P	HPO:iea[2009-02-17]
OMIM:267400	Renal, genital, and middle ear anomalies		HP:0000007	OMIM:267400	IEA					I	HPO:iea[2009-02-17]
OMIM:267400	Renal, genital, and middle ear anomalies		HP:0008678	OMIM:267400	IEA					P	HPO:iea[2009-02-17]
OMIM:267400	Renal, genital, and middle ear anomalies		HP:0000148	OMIM:267400	IEA					P	HPO:iea[2009-02-17]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0001297	PMID:16178030	PCS		4/4			P	HPO:probinson[2012-04-10];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0003401	PMID:16178030	PCS		1/4			P	HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0003596	PMID:16178030	PCS		1/4			C	HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0011970	PMID:16178030	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0011695	PMID:16178030	PCS		4/4			P	HPO:probinson[2012-04-10];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0003584	PMID:16178030	PCS		3/4			C	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0000726	PMID:16178030	PCS		1/4			P	HPO:probinson[2012-04-10];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0004938	OMIM:605714	PCS					P	HPO:probinson[2012-04-10]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0004968	PMID:16178030	PCS		3/4			P	HPO:probinson[2012-04-10];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0002637	PMID:16178030	PCS					P	HPO:probinson[2012-04-10];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0000006	PMID:16178030	PCS					I	HPO:probinson[2012-04-10];HPO:probinson[2023-02-20]
OMIM:605714	Cerebral amyloid angiopathy, APP-related		HP:0002138	PMID:16178030	PCS		1/4			P	HPO:probinson[2023-02-20]
OMIM:618745	Spermatogenic failure 42		HP:0032560	PMID:31735292	PCS					P	HPO:probinson[2020-04-24]
OMIM:618745	Spermatogenic failure 42		HP:0032561	PMID:31735292	PCS					P	HPO:probinson[2020-04-24]
OMIM:618745	Spermatogenic failure 42		HP:0003251	PMID:31735292	PCS		5/5			P	HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:618745	Spermatogenic failure 42		HP:0032562	PMID:31735292	PCS					P	HPO:probinson[2020-04-24]
OMIM:618745	Spermatogenic failure 42		HP:0000007	PMID:31735292	PCS					I	HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:618745	Spermatogenic failure 42		HP:0012207	PMID:31735292	PCS		5/5			P	HPO:probinson[2020-04-24];HPO:probinson[2020-04-24]
OMIM:618745	Spermatogenic failure 42		HP:0032558	PMID:31735292	PCS					P	HPO:probinson[2020-04-24]
OMIM:618745	Spermatogenic failure 42		HP:0032559	PMID:31735292	PCS					P	HPO:probinson[2020-04-24]
OMIM:601214	Naxos disease		HP:0002224	PMID:11691526	PCS	HP:0003577	28/28			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0002224	PMID:20130592	PCS		5/5			P	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0002224	PMID:32212272	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0003577	PMID:32212272	PCS		1/1			C	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0001030	PMID:20130592	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0011712	PMID:11691526	PCS					P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0011675	PMID:20130592	PCS		0/5			P	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0045075	OMIM:601214	TAS					P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0100792	PMID:32212272	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0008392	PMID:32212272	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0031193	PMID:11691526	PCS		23/26			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0001806	OMIM:601214	TAS					P	HPO:skoehler[2015-11-15]
OMIM:601214	Naxos disease		HP:0001627	PMID:20130592	PCS		0/5			P	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0001962	PMID:11691526	PCS		2/26			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0006677	PMID:11691526	PCS		19/26			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0007447	PMID:32212272	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0001645	PMID:11691526	PCS					P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0001644	OMIM:601214	IEA					P	HPO:iea[2009-02-17]
OMIM:601214	Naxos disease		HP:0002212	OMIM:601214	IEA					P	HPO:iea[2009-02-17]
OMIM:601214	Naxos disease		HP:0004751	PMID:11691526	PCS					P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0001640	OMIM:601214	IEA					P	HPO:iea[2009-02-17]
OMIM:601214	Naxos disease		HP:0002231	OMIM:601214	IEA					P	HPO:skoehler[2019-09-07]
OMIM:601214	Naxos disease		HP:0025092	PMID:32212272	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0010872	PMID:11691526	PCS		20/26			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0011663	PMID:32212272	PCS		1/1			P	HPO:probinson[2018-01-28];HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0008066	PMID:32212272	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0006682	PMID:11691526	PCS		24/26			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0001635	PMID:11691526	PCS					P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0000007	PMID:20130592	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0004308	PMID:11691526	PCS					P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0008404	OMIM:601214	TAS					P	HPO:skoehler[2015-11-15]
OMIM:601214	Naxos disease		HP:0001279	PMID:11691526	PCS		15/26			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0000982	PMID:20130592	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:601214	Naxos disease		HP:0000982	PMID:11691526	PCS	HP:0003577	28/28			P	HPO:probinson[2018-01-28]
OMIM:601214	Naxos disease		HP:0001699	OMIM:601214	IEA					P	HPO:iea[2009-02-17]
OMIM:601214	Naxos disease		HP:0000962	PMID:32212272	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:125853	Diabetes mellitus, noninsulin-dependent		HP:0003584	OMIM:125853	TAS					C	HPO:probinson[2009-02-17]
OMIM:125853	Diabetes mellitus, noninsulin-dependent		HP:0031819	OMIM:125853	TAS					P	HPO:lccarmody[2020-03-11]
OMIM:125853	Diabetes mellitus, noninsulin-dependent		HP:0000855	OMIM:125853	TAS					P	HPO:probinson[2009-02-17]
OMIM:125853	Diabetes mellitus, noninsulin-dependent		HP:0005978	OMIM:125853	TAS					P	HPO:probinson[2009-02-17]
OMIM:125853	Diabetes mellitus, noninsulin-dependent		HP:0000006	OMIM:125853	TAS					I	HPO:probinson[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0002014	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0002243	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0002573	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0002024	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0000007	OMIM:277175	IEA					I	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0002617	OMIM:277175	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277175	Vascular hyalinosis		HP:0002216	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0002514	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0007777	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0001029	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:277175	Vascular hyalinosis		HP:0002138	OMIM:277175	IEA					P	HPO:iea[2009-02-17]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000286	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000486	PMID:20817137	PCS		1/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0004322	OMIM:613610	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000083	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0010442	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0045075	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000639	PMID:20817137	PCS		0/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001408	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000319	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000316	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0007687	PMID:20817137	PCS		1/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001643	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0002613	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000476	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000278	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001249	PMID:20817137	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0020206	PMID:20817137	PCS		2/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000175	OMIM:613610	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000293	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001382	OMIM:613610	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001263	OMIM:613610	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000691	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0011800	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0006580	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000968	OMIM:613610	IEA					P	HPO:skoehler[2015-01-14]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0002904	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0011330	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000888	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000767	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000007	PMID:20817137	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0030151	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000289	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000369	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001655	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000687	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0011090	PMID:20817137	PCS		2/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000341	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001396	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000582	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0003577	PMID:20817137	PCS		2/2			C	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0008905	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001156	PMID:20817137	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000023	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000540	PMID:20817137	PCS		1/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000581	OMIM:613610	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0002240	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0008070	PMID:20817137	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001789	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001748	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0030084	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000218	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0006532	PMID:20817137	PCS		1/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000774	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000653	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0002910	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000773	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000256	PMID:20817137	PCS		1/2			P	HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0002676	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001744	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000973	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001363	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0003027	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001561	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000431	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000232	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001162	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000470	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0045025	PMID:20817137	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0005280	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000506	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000822	OMIM:613610	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000107	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000348	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001712	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000268	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0002007	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001357	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001159	PMID:20817137	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0001631	OMIM:613610	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613610	Cranioectodermal dysplasia 2		HP:0000347	PMID:20817137	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:604387	Nephronophthisis 3		HP:0003774	PMID:12872122	PCS					P	HPO:probinson[2022-11-20];HPO:probinson[2022-11-20]
OMIM:604387	Nephronophthisis 3		HP:0003774	PMID:19177160	PCS	HP:0011463	16/16			P	HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0005576	PMID:19177160	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-20];HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0000083	PMID:12872122	PCS	HP:0011462				P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-20]
OMIM:604387	Nephronophthisis 3		HP:0000790	PMID:19177160	PCS		0/16			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0001395	PMID:19177160;PMID:12872122	PCS		6/53			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10];HPO:probinson[2022-11-20]
OMIM:604387	Nephronophthisis 3		HP:0003593	PMID:19177160	PCS		12/16			C	HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0000090	PMID:19177160	PCS		16/16			P	HPO:skoehler[2015-01-27];HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0000093	PMID:19177160	PCS		0/16			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0000092	PMID:12872122	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-20]
OMIM:604387	Nephronophthisis 3		HP:0001508	PMID:19177160	PCS		11/16			P	HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0001959	PMID:19177160	PCS		7/16			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0011463	PMID:19177160	PCS		4/16			C	HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0000805	OMIM:604387	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604387	Nephronophthisis 3		HP:0000007	PMID:12872122	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-20]
OMIM:604387	Nephronophthisis 3		HP:0000108	PMID:12872122	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-20]
OMIM:604387	Nephronophthisis 3		HP:0000103	PMID:19177160	PCS		7/16			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:604387	Nephronophthisis 3		HP:0000105	PMID:19177160	PCS		7/16			P	HPO:probinson[2024-03-10]
OMIM:256150	NEPHROSIALIDOSIS		HP:0000112	OMIM:256150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256150	NEPHROSIALIDOSIS		HP:0000100	OMIM:256150	IEA					P	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0001541	OMIM:256150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256150	NEPHROSIALIDOSIS		HP:0004333	OMIM:256150	IEA					P	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0000083	OMIM:256150	IEA					P	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0003593	OMIM:256150	TAS					C	HPO:skoehler[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0003819	OMIM:256150	IEA					C	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0000924	OMIM:256150	IEA					P	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0001939	OMIM:256150	IEA					P	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0001999	OMIM:256150	IEA					P	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0000007	OMIM:256150	IEA					I	HPO:iea[2009-02-17]
OMIM:256150	NEPHROSIALIDOSIS		HP:0001698	OMIM:256150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613823	Seckel syndrome 5		HP:0000340	PMID:21131973	PCS		8/8			P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0003577	PMID:21131973	PCS		8/8			C	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000486	PMID:21131973	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0004322	PMID:21131973	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000581	PMID:21131973	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0001592	PMID:21131973	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0006297	PMID:21131973	PCS		2/6			P	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000878	PMID:21131973	PCS		5/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000218	PMID:21131973	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0002536	PMID:21131973	PCS					P	HPO:probinson[2013-08-10]
OMIM:613823	Seckel syndrome 5		HP:0001763	PMID:21131973	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000278	PMID:21131973	PCS					P	HPO:probinson[2013-08-10]
OMIM:613823	Seckel syndrome 5		HP:0001249	PMID:21131973	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000677	PMID:21131973	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000175	PMID:21131973	PCS		1/8			P	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000494	PMID:21131973	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000252	PMID:21131973	PCS					P	HPO:probinson[2013-08-10]
OMIM:613823	Seckel syndrome 5		HP:0002650	PMID:21131973	PCS		1/7			P	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0002750	PMID:21131973	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0005819	PMID:21131973	PCS		0/7			P	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000668	PMID:21131973	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000426	PMID:21131973	PCS					P	HPO:probinson[2013-08-10]
OMIM:613823	Seckel syndrome 5		HP:0000007	PMID:21131973	PCS					I	HPO:probinson[2013-01-09]
OMIM:613823	Seckel syndrome 5		HP:0004209	PMID:21131973	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0008665	PMID:21131973	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000444	PMID:21131973	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000047	PMID:21131973	PCS		1/5			P	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000028	PMID:21131973	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000369	PMID:21131973	PCS		6/8			P	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000347	PMID:21131973	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0000324	PMID:21131973	PCS		2/8			P	HPO:probinson[2023-01-23]
OMIM:613823	Seckel syndrome 5		HP:0009879	PMID:21131973	PCS		5/5			P	HPO:probinson[2023-01-23]
OMIM:312060	Properdin deficiency, X-linked		HP:0005423	OMIM:312060	IEA					P	HPO:iea[2009-02-17]
OMIM:312060	Properdin deficiency, X-linked		HP:0001419	OMIM:312060	IEA					I	HPO:iea[2009-02-17]
OMIM:312060	Properdin deficiency, X-linked		HP:0001939	OMIM:312060	IEA					P	HPO:iea[2009-02-17]
OMIM:620231	Short QT syndrome 7		HP:0012232	PMID:29167417	PCS					P	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:620231	Short QT syndrome 7		HP:0003621	PMID:29167417	PCS					C	HPO:probinson[2023-03-31]
OMIM:620231	Short QT syndrome 7		HP:0001663	PMID:29167417	PCS					P	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:620231	Short QT syndrome 7		HP:0001695	PMID:29167417	PCS					P	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:620231	Short QT syndrome 7		HP:0011462	PMID:29167417	PCS					C	HPO:probinson[2023-03-31]
OMIM:620231	Short QT syndrome 7		HP:0001279	PMID:29167417	PCS					P	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:620231	Short QT syndrome 7		HP:0000006	PMID:29167417	PCS					I	HPO:probinson[2023-03-31]
OMIM:620231	Short QT syndrome 7		HP:0001645	PMID:29167417	PCS					P	HPO:probinson[2023-03-31];HPO:probinson[2023-03-31]
OMIM:268900	SARCOSINEMIA		HP:0010896	OMIM:268900	IEA					P	HPO:iea[2009-02-17]
OMIM:268900	SARCOSINEMIA		HP:0000007	OMIM:268900	IEA					I	HPO:iea[2009-02-17]
OMIM:192800	Vertebral fusion, posterior lumbosacral, with blepharoptosis		HP:0001939	OMIM:192800	IEA					P	HPO:iea[2009-02-17]
OMIM:192800	Vertebral fusion, posterior lumbosacral, with blepharoptosis		HP:0007970	OMIM:192800	IEA					P	HPO:iea[2009-02-17]
OMIM:192800	Vertebral fusion, posterior lumbosacral, with blepharoptosis		HP:0005626	OMIM:192800	IEA					P	HPO:iea[2009-02-17]
OMIM:192800	Vertebral fusion, posterior lumbosacral, with blepharoptosis		HP:0000006	OMIM:192800	IEA					I	HPO:iea[2009-02-17]
OMIM:212060	Carbimazole sensitivity		HP:0000007	OMIM:212060	IEA					I	HPO:iea[2009-02-17]
OMIM:212060	Carbimazole sensitivity		HP:0012235	OMIM:212060	TAS					P	HPO:probinson[2013-03-31]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0001344	PMID:28098945;PMID:25223753	PCS		3/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0000750	PMID:28098945;PMID:25223753	PCS		11/12			P	HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0031936	PMID:25223753	PCS		4/6			P	HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0001250	PMID:28098945;PMID:25223753	PCS		9/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0002120	PMID:25223753	PCS		1/6		HP:0012825	P	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0002373	PMID:28098945	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0001263	PMID:28098945;PMID:25223753	PCS		9/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0030891	PMID:25223753	PCS		1/6			P	HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0100710	PMID:25223753	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0031491	PMID:28098945;PMID:25223753	PCS		6/9			P	HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0001328	PMID:28098945	PCS		1/4			P	HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0001417	PMID:25223753	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0000752	PMID:28098945;PMID:25223753	PCS		10/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:301008	Intellectual developmental disorder, X-linked syndromic, Houge type		HP:0007018	PMID:28098945;PMID:25223753	PCS		10/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0002487	OMIM:233910	TAS					P	HPO:skoehler[2012-10-17]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001254	OMIM:233910	IEA					P	HPO:skoehler[2010-06-18]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0002344	OMIM:233910	IEA					P	HPO:skoehler[2010-06-20]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001332	PMID:7869202	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001250	PMID:7730309	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001252	PMID:7730309	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0002063	OMIM:233910	IEA					P	HPO:skoehler[2010-06-18]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0006829	OMIM:233910	IEA					P	HPO:iea[2009-02-17]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0003593	PMID:7869202	PCS		1/1			C	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001290	PMID:7869202	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0000737	OMIM:233910	IEA					P	HPO:skoehler[2010-06-18]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0040417	PMID:7730309	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0500223	PMID:7869202	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0003623	PMID:7730309	PCS		1/1			C	HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:6000120	OMIM:233910	TAS					P	HPO:probinson[2024-01-06]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0002015	OMIM:233910	IEA					P	HPO:skoehler[2010-06-18]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0000496	OMIM:233910	IEA					P	HPO:skoehler[2010-06-18]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001266	PMID:7730309	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0003781	OMIM:233910	TAS					P	HPO:skoehler[2015-01-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0011968	PMID:7730309	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0002033	PMID:7730309	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001263	PMID:7869202;PMID:7730309	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2024-01-13];HPO:skoehler[2010-06-18];HPO:probinson[2023-03-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0040420	PMID:7730309	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0002509	OMIM:233910	IEA					P	HPO:iea[2009-02-17]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0000007	PMID:7869202	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001954	OMIM:233910	IEA					P	HPO:skoehler[2010-06-18]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0004923	PMID:7869202;PMID:7730309	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2024-01-13];HPO:probinson[2023-03-04]
OMIM:233910	Hyperphenylalaninemia, BH4-deficient, B		HP:0001337	PMID:7869202	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-04]
OMIM:137270	Gastrocutaneous syndrome		HP:0002036	OMIM:137270	IEA					P	HPO:iea[2009-02-17]
OMIM:137270	Gastrocutaneous syndrome		HP:0001003	OMIM:137270	IEA					P	HPO:iea[2009-02-17]
OMIM:137270	Gastrocutaneous syndrome		HP:0004398	OMIM:137270	IEA					P	HPO:iea[2009-02-17]
OMIM:137270	Gastrocutaneous syndrome		HP:0000957	OMIM:137270	IEA					P	HPO:iea[2009-02-17]
OMIM:137270	Gastrocutaneous syndrome		HP:0000316	OMIM:137270	IEA					P	HPO:iea[2009-02-17]
OMIM:137270	Gastrocutaneous syndrome		HP:0000006	OMIM:137270	IEA					I	HPO:iea[2009-02-17]
OMIM:137270	Gastrocutaneous syndrome		HP:0000545	OMIM:137270	IEA					P	HPO:iea[2009-02-17]
OMIM:607842	Aural atresia, congenital		HP:0004409	PMID:22152683	PCS					P	HPO:skoehler[2015-04-05];HPO:probinson[2023-04-09]
OMIM:607842	Aural atresia, congenital		HP:0000405	PMID:22152683	PCS				HP:0012832	P	HPO:skoehler[2015-04-05];HPO:probinson[2023-04-09]
OMIM:607842	Aural atresia, congenital		HP:0000413	PMID:22152683	PCS					P	HPO:probinson[2013-01-09]
OMIM:607842	Aural atresia, congenital		HP:0000006	PMID:22152683	PCS					I	HPO:probinson[2013-03-04]
OMIM:604393	Leber congenital amaurosis 4		HP:0000563	OMIM:604393	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:604393	Leber congenital amaurosis 4		HP:0000662	OMIM:604393	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:604393	Leber congenital amaurosis 4		HP:0012043	OMIM:604393	TAS					P	HPO:probinson[2012-08-01]
OMIM:604393	Leber congenital amaurosis 4		HP:0000618	OMIM:604393	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604393	Leber congenital amaurosis 4		HP:0000007	OMIM:604393	TAS					I	HPO:probinson[2012-08-01]
OMIM:604393	Leber congenital amaurosis 4		HP:0007663	OMIM:604393	TAS					P	HPO:probinson[2012-08-01]
OMIM:604393	Leber congenital amaurosis 4		HP:0007401	OMIM:604393	TAS					P	HPO:probinson[2012-08-01]
OMIM:604393	Leber congenital amaurosis 4		HP:0000548	OMIM:604393	IEA					P	HPO:skoehler[2015-01-19]
OMIM:604393	Leber congenital amaurosis 4		HP:0000543	OMIM:604393	TAS					P	HPO:probinson[2012-08-01]
OMIM:604393	Leber congenital amaurosis 4		HP:0007688	OMIM:604393	TAS					P	HPO:probinson[2012-08-01]
OMIM:604393	Leber congenital amaurosis 4		HP:0007843	OMIM:604393	TAS				HP:0012828	P	HPO:probinson[2012-08-01]
OMIM:604393	Leber congenital amaurosis 4		HP:0000006	OMIM:604393	TAS					I	HPO:probinson[2020-07-19]
OMIM:614180	Retinitis pigmentosa 61		HP:0007737	PMID:21310491	PCS					P	HPO:probinson[2013-02-23]
OMIM:614180	Retinitis pigmentosa 61		HP:0000662	PMID:21310491	PCS					P	HPO:probinson[2013-02-23]
OMIM:614180	Retinitis pigmentosa 61		HP:0000007	PMID:21310491	PCS					I	HPO:probinson[2013-01-09]
OMIM:614180	Retinitis pigmentosa 61		HP:0000505	PMID:21310491	PCS					P	HPO:probinson[2013-02-23]
OMIM:614180	Retinitis pigmentosa 61		HP:0007688	PMID:21310491	PCS					P	HPO:probinson[2013-02-23]
OMIM:614180	Retinitis pigmentosa 61		HP:0000510	OMIM:614180	TAS					P	HPO:skoehler[2015-01-19]
OMIM:614180	Retinitis pigmentosa 61		HP:0007843	PMID:21310491	PCS					P	HPO:probinson[2013-02-23]
OMIM:613837	Leber congenital amaurosis 11		HP:0000639	PMID:16384941	PCS					P	HPO:probinson[2013-08-10]
OMIM:613837	Leber congenital amaurosis 11		HP:0007663	OMIM:613837	IEA					P	HPO:skoehler[2019-02-22]
OMIM:613837	Leber congenital amaurosis 11		HP:0000505	PMID:16384941	PCS					P	HPO:probinson[2013-08-10]
OMIM:613837	Leber congenital amaurosis 11		HP:0000006	PMID:16384941	PCS					I	HPO:probinson[2013-08-10]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000286	PMID:32001716	PCS		3/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0002521	PMID:32001716	IEA					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0002188	PMID:32001716	PCS					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0001332	PMID:32001716	PCS		5/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0001250	PMID:32001716	PCS		30/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000581	PMID:32001716	PCS					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0012745	PMID:32001716	PCS		3/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0001290	PMID:32001716	PCS		7/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000319	PMID:32001716	PCS		7/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0002119	PMID:32001716	IEA					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0025336	PMID:32001716	PCS		28/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000179	PMID:32001716	PCS		4/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0009748	PMID:32001716	PCS		1/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0001347	PMID:32001716	PCS		9/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0008936	PMID:32001716	PCS		35/60			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0002179	PMID:32001716	PCS		2/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000252	PMID:32001716	PCS		3/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0003487	PMID:32001716	PCS		2/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000490	PMID:32001716	PCS		1/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0001284	PMID:32001716	PCS		2/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0002072	PMID:32001716	IEA					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0010851	PMID:32001716	IEA					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0011344	PMID:32001716	PCS					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0011471	PMID:32001716	PCS		12/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0011097	PMID:32001716	PCS		16/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000508	PMID:32001716	PCS					P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000007	PMID:32001716	PCS					I	HPO:probinson[2020-05-08];HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000307	PMID:32001716	PCS		2/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0200134	PMID:32001716	PCS		27/30			P	HPO:probinson[2020-05-08];HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0001357	PMID:32001716	PCS		1/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0000664	PMID:32001716	PCS		2/30			P	HPO:probinson[2020-05-08]
OMIM:618792	Epileptic encephalopathy, early infantile, 84		HP:0001257	PMID:32001716	PCS		13/30			P	HPO:probinson[2020-05-08]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0003236	OMIM:160300	TAS					P	HPO:skoehler[2015-08-16]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0003376	OMIM:160300	TAS					P	HPO:skoehler[2015-08-16]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0008981	OMIM:160300	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0009025	OMIM:160300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0003593	OMIM:160300	TAS					C	HPO:probinson[2009-02-17]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0002460	OMIM:160300	TAS					P	HPO:probinson[2013-12-16]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0009027	OMIM:160300	TAS					P	HPO:probinson[2009-02-17]
OMIM:160300	Myopathy, distal, infantile-onset		HP:0000006	OMIM:160300	TAS					I	HPO:probinson[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0003577	PMID:26336027	PCS		1/1			C	HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0001773	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000343	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0001250	PMID:26336027	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0012448	OMIM:241410	TAS					P	HPO:skoehler[2017-07-13]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0008198	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0011220	OMIM:241410	TAS					P	HPO:skoehler[2012-10-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002718	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002119	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000219	PMID:26336027	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0008897	OMIM:241410	TAS					P	HPO:skoehler[2012-10-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000358	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0001249	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0008936	PMID:26336027	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000054	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000252	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000233	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0004279	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002199	PMID:26336027	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0005686	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002079	OMIM:241410	TAS					P	HPO:skoehler[2017-07-13]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002750	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000490	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0031817	PMID:26336027	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000193	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0001281	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0005280	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002905	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000568	PMID:26336027	PCS		1/1			P	HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000007	OMIM:241410	IEA					I	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000824	OMIM:241410	TAS					P	HPO:skoehler[2017-07-13]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002901	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0200055	OMIM:241410	TAS					P	HPO:skoehler[2012-10-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0002007	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000444	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0008846	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000347	PMID:26336027	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-15]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000369	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:241410	Hypoparathyroidism-retardation-dysmorphism syndrome		HP:0000028	OMIM:241410	IEA					P	HPO:iea[2009-02-17]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0005116	PMID:25163805;PMID:22772371	PCS		11/18			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000023	PMID:22772368;PMID:25163805;PMID:22772371	PCS		26/42			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0003179	PMID:22772371	PCS		1/8			P	HPO:probinson[2021-05-22]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0010809	PMID:22772368	PCS		2/15			P	HPO:probinson[2019-07-13]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0025643	PMID:22772368	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0410151	PMID:23608731	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0002619	PMID:22772368	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0002616	PMID:22772368;PMID:22772371	PCS		23/25			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001647	PMID:25046559;PMID:22772368;PMID:22772371	PCS		3/31			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000316	PMID:22772368;PMID:22772371	PCS		5/28			P	HPO:probinson[2021-05-23];HPO:skoehler[2012-11-18];HPO:probinson[2019-07-13]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000978	PMID:22772368;PMID:25163805	PCS		12/26			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0004419	PMID:22772371	PCS		2/18			P	HPO:probinson[2021-05-22]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0007720	PMID:22772371	PCS		2/8			P	HPO:probinson[2021-05-22]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000218	PMID:25046559;PMID:22772368;PMID:25163805;PMID:22772371	PCS		44/73			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];HPO:probinson[2021-05-23];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000977	PMID:22772368	PCS		3/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001763	PMID:25046559;PMID:22772368;PMID:25163805;PMID:22772371	PCS		42/73			P	HPO:probinson[2021-05-22];HPO:probinson[2024-03-31];HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000278	PMID:22772368;PMID:22772371	PCS		13/28			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-13];HPO:probinson[2021-05-23]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000974	PMID:25163805	PCS		2/15			P	HP:probinson[2019-05-14]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000973	PMID:22772371	PCS		0/13			P	HPO:probinson[2021-05-22]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001166	PMID:22772368;PMID:25163805;PMID:22772371	PCS		35/66			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000473	PMID:22772368	PCS		2/15			P	HPO:probinson[2019-07-13]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000494	PMID:22772368;PMID:22772371	PCS		10/28			P	HPO:skoehler[2012-11-20];HPO:probinson[2019-07-13];HPO:probinson[2021-05-23]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0003302	PMID:22772368;PMID:22772371	PCS		2/22			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-07-13];HPO:probinson[2021-05-22]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000098	PMID:22772368;PMID:25163805;PMID:22772371	PCS		33/59			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0002650	PMID:25046559;PMID:22772368;PMID:25163805;PMID:22772371	PCS		25/74			P	HPO:probinson[2021-05-22];HPO:probinson[2024-03-31];HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001762	PMID:22772368;PMID:25163805	PCS		11/55			P	HPO:skoehler[2012-11-18];HP:probinson[2019-05-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0004970	PMID:25046559	PCS		3/3			P	HPO:probinson[2021-05-23]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001382	PMID:25046559;PMID:22772368;PMID:25163805;PMID:22772371	PCS		43/74			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];HPO:probinson[2021-05-23];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000193	PMID:22772368	PCS		3/3			P	HPO:probinson[2019-07-13];HPO:probinson[2024-03-31]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000490	PMID:22772371	PCS		0/13			P	HPO:probinson[2021-05-23]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001065	PMID:22772368;PMID:25163805;PMID:22772371	PCS		24/70			P	HP:probinson[2019-05-14];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0002097	PMID:22772371	PCS		2/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-23]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000272	PMID:22772371	PCS		0/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001083	PMID:22772368;PMID:22772371	PCS		0/27			P	HPO:probinson[2021-05-22];HPO:probinson[2024-03-31];HPO:skoehler[2013-05-31];HPO:probinson[2019-07-13];HPO:probinson[2024-03-05]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0012532	PMID:25163805	PCS		2/2			P	HP:probinson[2019-05-14]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0100775	PMID:22772368;PMID:25163805;PMID:22772371	PCS		9/24			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000508	PMID:22772368	PCS		2/15			P	HPO:probinson[2019-07-13]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000766	PMID:22772368;PMID:22772371	PCS		16/31			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0002705	PMID:22772368	PCS		10/15			P	HPO:probinson[2019-07-13]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0002647	PMID:22772368;PMID:25163805	PCS		9/60			P	HPO:skoehler[2012-10-17];HP:probinson[2019-05-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0006687	PMID:22772371	PCS		3/5			P	HPO:probinson[2021-05-22]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000268	PMID:25046559	PCS		1/3			P	HPO:probinson[2021-05-23]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0004944	PMID:22772371	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0002107	PMID:22772371	PCS		1/17			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-22]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0000006	PMID:22772368;PMID:22772371	PCS		20/20			I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614816	Loeys-Dietz syndrome 4		HP:0001634	PMID:22772368;PMID:22772371	PCS		7/26			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0002069	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0002123	PMID:17262856	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001272	PMID:19185523	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001250	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001252	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001251	PMID:19185523	PCS		3/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0002141	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0003593	PMID:17262856	PCS		2/2			C	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001290	PMID:17262856	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0002381	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0000639	PMID:17262856	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0011463	PMID:19185523	PCS		3/3			C	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0002317	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0002359	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0003701	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0000510	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001249	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0008936	PMID:17262856	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001265	PMID:17262856	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0000750	PMID:17262856	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001266	PMID:17262856	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0031936	PMID:19185523	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001263	PMID:17262856	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0002151	PMID:19185523	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0011923	PMID:19185523;PMID:17262856	PCS		3/3			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0000408	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0000726	PMID:19185523	PCS		2/3			P	HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001419	PMID:17262856	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:301020	Mitochondrial complex I deficiency, nuclear type 12		HP:0001336	PMID:19185523	PCS		1/3			P	HPO:probinson[2023-02-18]
OMIM:257500	Obesity-Hypoventilation syndrome		HP:0002791	OMIM:257500	IEA					P	HPO:skoehler[2015-01-27]
OMIM:257500	Obesity-Hypoventilation syndrome		HP:0001262	OMIM:257500	IEA					P	HPO:iea[2009-02-17]
OMIM:257500	Obesity-Hypoventilation syndrome		HP:0000007	OMIM:257500	IEA					I	HPO:iea[2009-02-17]
OMIM:257500	Obesity-Hypoventilation syndrome		HP:0000961	OMIM:257500	IEA					P	HPO:iea[2009-02-17]
OMIM:257500	Obesity-Hypoventilation syndrome		HP:0001513	OMIM:257500	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0007759	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003277	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000365	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000683	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003311	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003593	PMID:32024277;PMID:35477222	PCS		2/2			C	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000280	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0012070	OMIM:253000	TAS					P	HPO:probinson[2012-08-04]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0008454	PMID:32024277	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003307	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003308	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002857	PMID:35477222	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:4000007	PMID:35477222	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0001249	PMID:32024277	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003521	PMID:35477222	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0030865	PMID:24602160	PCS					P	HPO:probinson[2017-05-27]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003049	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0001223	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002673	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0001382	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0012069	OMIM:253000	TAS					P	HPO:probinson[2012-08-04]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000926	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000007	OMIM:253000	TAS					I	HPO:probinson[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000768	PMID:35477222	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0001654	OMIM:253000	TAS					P	HPO:probinson[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000884	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002788	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000687	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003016	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000023	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003053	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002240	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0001270	PMID:32024277	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000939	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0008430	PMID:32024277	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002515	PMID:32024277	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002318	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0006532	PMID:35477222	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000154	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000670	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003621	OMIM:253000	IEA					C	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002650	PMID:35477222	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0031936	PMID:32024277	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0003300	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000470	PMID:35477222	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002091	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0002808	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000904	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000943	PMID:32024277	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:253000	Mucopolysaccharidosis IVA		HP:0000303	OMIM:253000	IEA					P	HPO:iea[2009-02-17]
OMIM:159595	Myeloproliferative syndrome, transient		HP:0005534	OMIM:159595	IEA					P	HPO:iea[2009-02-17]
OMIM:159595	Myeloproliferative syndrome, transient		HP:0001974	OMIM:159595	IEA					P	HPO:iea[2009-02-17]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001176	PMID:31736240	PCS					P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001274	PMID:31736240	PCS	HP:0003577	1/8			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001290	PMID:31736240	PCS		6/11			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0011220	PMID:31736240	PCS		7/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001548	PMID:31736240	PCS		12/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000316	PMID:31736240	PCS		10/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000998	PMID:31736240	PCS		3/11			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0030084	PMID:31736240	PCS					P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000256	PMID:31736240	PCS		8/12			P	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000311	PMID:31736240	PCS		8/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000336	PMID:31736240	PCS		5/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001249	PMID:31736240	PCS		7/12			P	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000995	PMID:31736240	PCS		2/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001545	PMID:31736240	PCS	HP:0003577	1/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000098	PMID:31736240	PCS					P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000494	PMID:31736240	PCS		6/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001263	PMID:31736240	PCS		10/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0012811	PMID:31736240	PCS					P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0012385	PMID:31736240	PCS					P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001537	PMID:31736240	PCS		4/11			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0001833	PMID:31736240	PCS					P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0003517	PMID:31736240	PCS		3/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0005616	PMID:31736240	PCS		6/8			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000006	PMID:31736240	PCS					I	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000303	PMID:31736240	PCS		2/13			P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0000028	PMID:31736240	PCS		4/8	MALE		P	HPO:probinson[2020-05-10]
OMIM:618786	Imagawa-Matsumoto syndrome		HP:0002126	PMID:31736240	PCS		1/13			P	HPO:probinson[2020-05-10]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002069	PMID:27108799	PCS		3/13			P	HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002301	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002540	PMID:27108799	PCS		3/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001377	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000486	PMID:27108799	PCS		4/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001332	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002384	PMID:27108799	PCS		3/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001250	PMID:27108799	PCS		10/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001252	PMID:27108799	PCS		11/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0003593	PMID:27108799	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0010841	PMID:27108799	PCS		5/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0032794	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0004283	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0005490	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0012469	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000639	PMID:27108799	PCS		3/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000718	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000717	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001763	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001249	PMID:27108799	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000358	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001188	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000011	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000175	PMID:27108799	PCS		2/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0006813	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002474	PMID:27108799	PCS		4/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0011968	PMID:27108799	PCS		4/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001382	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001263	PMID:27108799	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0100021	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001182	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001181	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0011289	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0012018	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0011210	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000407	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002509	PMID:27108799	PCS		4/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000767	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000565	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0007359	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000322	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000006	PMID:27108799	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000126	PMID:27108799	PCS		2/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001336	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002521	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0010307	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002121	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002283	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0012448	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0100035	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0100034	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000617	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001508	PMID:27108799	PCS		4/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0100704	PMID:27108799	PCS		3/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0007340	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000739	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000218	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000851	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000256	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000577	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001347	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000396	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0008936	PMID:27108799	PCS	HP:0003593	2/13			P	HPO:probinson[2025-02-23]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002015	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000750	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002133	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002376	PMID:27108799	PCS		3/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002373	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002099	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0010819	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002451	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0010818	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000074	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0010851	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0000708	PMID:27108799	PCS		4/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0011198	PMID:27108799	PCS		3/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0011352	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0032792	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0007772	PMID:27108799	PCS		1/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0007018	PMID:27108799	PCS		2/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0001510	PMID:27108799	PCS		6/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:616973	Intellectual developmental disorder, autosomal dominant 42		HP:0002126	PMID:27108799	PCS		1/13			P	HPO:probinson[2022-04-18];HPO:probinson[2022-04-18]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0003236	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:6000374	PMID:34819510	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0030356	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001250	PMID:33727065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0410174	PMID:33727065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001394	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0003593	PMID:33727065	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:6000239	PMID:34819510	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0031545	PMID:34819510	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0033106	PMID:33727065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0031964	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0008151	PMID:33727065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001409	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0033199	PMID:34819510	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001888	PMID:34819510;PMID:33727065	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001945	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0025435	PMID:33727065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001744	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0040218	PMID:34819510	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0004315	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0003623	PMID:34819510	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0002135	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0031956	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0030149	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001640	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0030783	PMID:34819510	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0002092	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0034447	PMID:34819510	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0003281	PMID:34819510;PMID:33727065	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0033833	PMID:34819510	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0002090	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0011227	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0033438	PMID:33727065	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0500271	PMID:34819510	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0011171	PMID:34819510;PMID:33727065	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0031185	PMID:34819510	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0100614	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0002922	PMID:34819510;PMID:33727065	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0000988	PMID:34819510;PMID:33727065	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001876	PMID:34819510;PMID:33727065	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0000006	PMID:34819510	PCS					I	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620796	Proteasome-associated autoinflammatory syndrome 6		HP:0001974	PMID:34819510;PMID:33727065	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:183500	Split-Hand and split-foot with hypodontia		HP:0001839	OMIM:183500	IEA					P	HPO:iea[2009-02-17]
OMIM:183500	Split-Hand and split-foot with hypodontia		HP:0000668	OMIM:183500	IEA					P	HPO:iea[2009-02-17]
OMIM:183500	Split-Hand and split-foot with hypodontia		HP:0001171	OMIM:183500	IEA					P	HPO:iea[2009-02-17]
OMIM:183500	Split-Hand and split-foot with hypodontia		HP:0000006	OMIM:183500	IEA					I	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0001342	OMIM:610655	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0006548	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0001694	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002642	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002076	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002140	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002094	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0011934	OMIM:610655	TAS					P	HPO:probinson[2012-06-10]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002390	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0100858	OMIM:610655	TAS					P	HPO:probinson[2012-06-10]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002707	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002408	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0000524	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0000227	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002626	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0000961	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0004406	OMIM:610655	IEA	HP:0003621				P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002326	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0000006	OMIM:610655	IEA					I	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0001722	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0000214	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0000434	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:610655	Telangiectasia, hereditary hemorrhagic, type 4		HP:0002138	OMIM:610655	IEA					P	HPO:iea[2009-02-17]
OMIM:107600	Aplasia cutis congenita, nonsyndromic		HP:0004471	PMID:23785305	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-07-17]
OMIM:107600	Aplasia cutis congenita, nonsyndromic		HP:0000006	PMID:23785305	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2020-07-17]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0002059	OMIM:609304	IEA					P	HPO:iea[2009-02-17]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0002123	PMID:15592994	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0001250	PMID:15592994	PCS		4/4			P	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0001252	PMID:15592994	PCS					P	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0005484	PMID:15592994	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0012448	OMIM:609304	TAS					P	HPO:skoehler[2014-05-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0010851	PMID:15592994	PCS		4/4			P	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0011421	PMID:15592994	PCS		1/4			C	HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0012444	PMID:15592994	PCS		2/4			P	HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0003819	OMIM:609304	IEA					C	HPO:iea[2009-02-17]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0000649	PMID:15592994	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0000007	PMID:15592994	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0001319	PMID:15592994	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0200134	PMID:15592994	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0001257	PMID:15592994	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:609304	Epileptic encephalopathy, early infantile, 3		HP:0003623	PMID:15592994	PCS		4/4			C	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0003577	PMID:24610330	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0010804	PMID:24610330	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0004322	OMIM:616224	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0011968	PMID:24610330	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0001252	PMID:24610330	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0003131	PMID:24610330	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0001270	OMIM:616224	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0030208	PMID:24610330	PCS		0/1			P	HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0000508	PMID:24610330	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0000007	PMID:24610330	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0000824	OMIM:616224	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0002515	PMID:24610330	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0001324	OMIM:616224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616224	Myasthenic syndrome, congenital, 22		HP:0003701	PMID:24610330	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:614433	Atrial septal defect 8		HP:0010772	PMID:16287139	PCS		1/2			P	HP:probinson[2019-01-20]
OMIM:614433	Atrial septal defect 8		HP:0001631	PMID:16287139	PCS		2/2			P	HPO:skoehler[2015-01-21];HP:probinson[2019-01-20]
OMIM:614433	Atrial septal defect 8		HP:0000006	PMID:16287139	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-01-20]
OMIM:603629	Deafness, autosomal recessive 21		HP:0000407	PMID:9949200	PCS	HP:0003593				P	HPO:probinson[2013-02-19]
OMIM:603629	Deafness, autosomal recessive 21		HP:0000007	PMID:9949200	PCS					I	HPO:probinson[2013-01-09]
OMIM:187000	Teeth, odd shapes oflobodontia, included		HP:0000164	OMIM:187000	IEA					P	HPO:iea[2009-02-17]
OMIM:187000	Teeth, odd shapes oflobodontia, included		HP:0000006	OMIM:187000	IEA					I	HPO:iea[2009-02-17]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0004798	PMID:11007475	PCS		18/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0200117	PMID:11007475	PCS					P	HPO:skoehler[2013-06-10];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0003496	PMID:11007475	PCS		15/18			P	HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0410295	PMID:11007475	PCS					P	HPO:probinson[2022-11-01];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0011463	PMID:11007475	PCS		18/18			C	HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0002959	PMID:11007475	PCS					P	HPO:probinson[2012-06-08];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0002718	PMID:11007475	PCS		18/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0000007	PMID:11007475	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0002716	PMID:11007475	PCS		13/18			P	HPO:probinson[2012-06-08];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0002205	PMID:11007475	PCS		18/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0002720	PMID:11007475	PCS		18/18			P	HPO:probinson[2012-06-08];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0002721	PMID:11007475	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:605258	Immunodeficiency with hyper-igm, type 2		HP:0004315	PMID:11007475	PCS		18/18			P	HPO:probinson[2012-06-08];HPO:probinson[2022-11-01]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000286	OMIM:103300	IEA					P	HPO:iea[2009-02-17]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000160	OMIM:103300	IEA					P	HPO:iea[2009-02-17]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000171	OMIM:103300	TAS					P	HPO:skoehler[2012-10-11]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0001171	OMIM:103300	IEA					P	HPO:iea[2009-02-17]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0009776	OMIM:103300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0012730	OMIM:103300	IEA					P	HPO:skoehler[2015-01-27]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0003745	OMIM:103300	TAS					I	HPO:skoehler[2015-12-30]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000278	OMIM:103300	IEA					P	HPO:iea[2009-02-17]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000006	OMIM:103300	IEA					I	HPO:iea[2009-02-17]
OMIM:103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000347	OMIM:103300	TAS					P	HPO:skoehler[2012-10-11]
OMIM:619665	Ovarian dysgenesis 9		HP:0008209	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0003621	PMID:27967308	PCS		2/2			C	HPO:probinson[2022-03-14]
OMIM:619665	Ovarian dysgenesis 9		HP:0000013	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0002750	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0011969	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0008232	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0000007	PMID:27967308	PCS					I	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0000823	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0008214	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0031103	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0000786	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:619665	Ovarian dysgenesis 9		HP:0008724	PMID:27967308;PMID:34697795	PCS		3/3			P	HPO:probinson[2022-02-12]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0001773	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0000233	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0004322	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0000771	PMID:19844254	PCS		1/3			P	HP:probinson[2018-07-05];HP:probinson[2018-07-14]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0000490	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0002231	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05];HP:probinson[2018-07-14]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0001263	OMIM:300869	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0040171	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05];HP:probinson[2018-07-14]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0012743	PMID:19844254	PCS					P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0000837	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05];HP:probinson[2018-07-14]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0001419	PMID:19844254	PCS					I	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0001518	OMIM:300869	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0001328	PMID:19844254	PCS	HP:0011463	3/3		HP:0012825	P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0000414	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0001511	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0200055	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0008734	PMID:19844254	PCS		3/3			P	HP:probinson[2018-07-05];HP:probinson[2018-07-14]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0000135	OMIM:300869	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0001620	OMIM:300869	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300869	Chromosome xq27.3-q28 duplication syndrome		HP:0000028	PMID:19844254	PCS	HP:0003577	3/3			P	HP:probinson[2018-07-05]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0005458	OMIM:610127	IEA					P	HPO:iea[2009-02-17]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0003577	PMID:16670177	PCS		4/4			C	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0000340	PMID:16670177	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0001272	PMID:25298308;PMID:16685649	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0001250	PMID:16670177	PCS		3/4			P	HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002063	OMIM:610127	IEA					P	HPO:iea[2009-02-17]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0001251	PMID:25298308;PMID:16685649	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0032794	PMID:16670177	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0003390	PMID:25298308	PCS		2/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0001171	PMID:16670177	PCS		1/4			P	HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0011463	PMID:16685649	PCS		1/1			C	HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002878	PMID:16670177	PCS		1/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0000510	PMID:25298308	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0001268	PMID:25298308;PMID:16685649	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0001105	PMID:16685649	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0000572	OMIM:610127	TAS					P	HPO:probinson[2009-02-17]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002059	PMID:16685649	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0000252	PMID:16670177	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002133	OMIM:610127	IEA					P	HPO:iea[2009-02-17]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0000431	PMID:16670177	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002074	OMIM:610127	IEA					P	HPO:iea[2009-02-17]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002093	OMIM:610127	IEA					P	HPO:iea[2009-02-17]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0000007	PMID:16685649	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002529	OMIM:610127	TAS					P	HPO:probinson[2012-07-16]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0003811	PMID:16670177	PCS		1/4			C	HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0003657	PMID:25298308	PCS		2/5			P	HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0001257	PMID:16670177	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0002104	PMID:16670177	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:610127	Ceroid lipofuscinosis, neuronal, 10		HP:0000369	PMID:16670177	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:608768	Spinocerebellar ataxia 8		HP:0002311	OMIM:608768	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0002015	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0001272	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0001260	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0002062	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0002073	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0000639	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0000514	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0007772	OMIM:608768	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608768	Spinocerebellar ataxia 8		HP:0009830	OMIM:608768	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608768	Spinocerebellar ataxia 8		HP:0007256	OMIM:608768	TAS					P	HPO:skoehler[2015-01-04]
OMIM:608768	Spinocerebellar ataxia 8		HP:0000763	OMIM:608768	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0000641	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0001257	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0000006	OMIM:608768	IEA					I	HPO:iea[2009-02-17]
OMIM:608768	Spinocerebellar ataxia 8		HP:0001337	OMIM:608768	IEA					P	HPO:iea[2009-02-17]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0003376	OMIM:600334	IEA					P	HPO:iea[2009-02-17]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0003581	PMID:12145747	PCS		71/71			C	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0003829	OMIM:600334	IEA					I	HPO:iea[2009-02-17]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0003560	OMIM:600334	TAS					P	HPO:skoehler[2015-01-21]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0003805	OMIM:600334	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0001638	PMID:12145747	PCS		0/71			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-09]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0008963	PMID:12145747	PCS		71/71			P	HPO:probinson[2024-03-09]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0011399	PMID:12145747	PCS		71/71			P	HPO:probinson[2024-03-09]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0000006	PMID:12145747	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0003677	OMIM:600334	TAS					C	HPO:skoehler[2009-02-17]
OMIM:600334	Tibial muscular dystrophy, tardive		HP:0003458	OMIM:600334	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0002301	PMID:37282399	PCS		2/2			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0001014	PMID:9762612;PMID:36352683	PCS		2/2			P	HPO:probinson[2023-07-08];HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0000365	PMID:36352683;PMID:8719750	PCS		1/2			P	HPO:probinson[2023-07-08];HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0001332	PMID:8719750	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0004322	PMID:9762612;PMID:36352683	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:230000	Fucosidosis		HP:0001371	PMID:9762612	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:230000	Fucosidosis		HP:0001250	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0005453	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0000240	PMID:9762612	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:230000	Fucosidosis		HP:0001252	PMID:36352683	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0010729	PMID:37282399	PCS		0/2			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0003593	PMID:37282399;PMID:8719750	PCS		5/5			C	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30];HPO:probinson[2023-07-08];HPO:probinson[2023-07-08];HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0002064	PMID:8719750	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0000280	PMID:36352683	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0000958	OMIM:230000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:230000	Fucosidosis		HP:0000914	OMIM:230000	TAS					P	HPO:skoehler[2014-06-24]
OMIM:230000	Fucosidosis		HP:0011220	OMIM:230000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:230000	Fucosidosis		HP:0002938	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0000316	PMID:37282399	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001922	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0003429	PMID:36352683	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0000158	OMIM:230000	TAS					P	HPO:probinson[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001324	PMID:8719750	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0004558	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001249	PMID:9762612	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0003700	PMID:9762612	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:230000	Fucosidosis		HP:0002510	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0000970	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0000574	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0002673	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001263	PMID:37282399;PMID:36352683;PMID:8719750	PCS		4/4			P	HPO:probinson[2022-04-30];HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0002194	PMID:36352683	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0012067	PMID:8719750	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0000007	PMID:9039984	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0000967	PMID:37282399	PCS		2/2			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0000369	PMID:37282399	PCS		2/2			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0004568	PMID:36352683	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0000445	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001552	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001271	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0002240	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0100790	OMIM:230000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:230000	Fucosidosis		HP:0001508	PMID:37282399	PCS		2/2			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0008430	PMID:8719750	PCS		1/1			P	HPO:probinson[2012-06-10];HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0010471	OMIM:230000	TAS					P	HPO:probinson[2013-03-13]
OMIM:230000	Fucosidosis		HP:0000978	PMID:37282399	PCS		2/2			P	HPO:probinson[2023-07-08];HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0008436	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001268	PMID:37282399;PMID:9762612	PCS		3/3			P	HPO:probinson[2023-07-08];HPO:probinson[2024-03-08]
OMIM:230000	Fucosidosis		HP:0000179	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001348	PMID:8719750	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0001744	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0002059	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0034727	PMID:2903668;PMID:9762612	PCS		11/11			P	HPO:probinson[2023-07-18];HPO:probinson[2023-06-05];HPO:probinson[2024-03-08]
OMIM:230000	Fucosidosis		HP:0002650	PMID:9762612	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0004630	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0001640	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0002376	PMID:8719750	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230000	Fucosidosis		HP:0003300	PMID:36352683	PCS		1/1			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0005280	PMID:37282399	PCS		2/2			P	HPO:probinson[2023-07-08]
OMIM:230000	Fucosidosis		HP:0012236	OMIM:230000	TAS					P	HPO:probinson[2013-03-31]
OMIM:230000	Fucosidosis		HP:0000943	PMID:37282399;PMID:9762612	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:230000	Fucosidosis		HP:0000503	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0002007	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:230000	Fucosidosis		HP:0002205	OMIM:230000	IEA					P	HPO:iea[2009-02-17]
OMIM:614341	Intellectual developmental disorder, autosomal recessive 33		HP:0001999	PMID:21937992	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2025-09-26]
OMIM:614341	Intellectual developmental disorder, autosomal recessive 33		HP:0000007	PMID:21063731	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2025-09-26]
OMIM:614341	Intellectual developmental disorder, autosomal recessive 33		HP:0001159	PMID:21937992	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2025-09-26]
OMIM:614341	Intellectual developmental disorder, autosomal recessive 33		HP:0001831	PMID:21937992	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2025-09-26]
OMIM:613348	Pancreatic cancer, susceptibility to, 3		HP:0006725	PMID:19264984	PCS					P	HPO:probinson[2024-07-07]
OMIM:613348	Pancreatic cancer, susceptibility to, 3		HP:0003581	PMID:19264984	PCS					C	HPO:probinson[2024-07-07]
OMIM:613348	Pancreatic cancer, susceptibility to, 3		HP:0000006	PMID:19264984	PCS					I	HPO:probinson[2024-07-07]
OMIM:115210	Cardiomyopathy, familial restrictive, 1		HP:0031295	PMID:12531876	PCS		3/9			P	HP:probinson[2019-03-09]
OMIM:115210	Cardiomyopathy, familial restrictive, 1		HP:0001723	PMID:12531876	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:115210	Cardiomyopathy, familial restrictive, 1		HP:0001712	PMID:12531876	PCS		6/9			P	HP:probinson[2019-03-09]
OMIM:115210	Cardiomyopathy, familial restrictive, 1		HP:0002119	PMID:12531876	PCS					P	HPO:skoehler[2010-06-20];HP:probinson[2019-03-09]
OMIM:115210	Cardiomyopathy, familial restrictive, 1		HP:0000006	PMID:12531876	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:115210	Cardiomyopathy, familial restrictive, 1		HP:0001645	PMID:12531876	PCS					P	HP:probinson[2019-03-09]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000483	PMID:35979925	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0002521	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0003577	PMID:35979925	PCS		1/12			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000486	PMID:35979925	PCS		3/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0001212	PMID:35979925	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000365	PMID:35979925	PCS		3/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000540	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0001195	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0002121	PMID:35979925	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0003593	PMID:35979925	PCS		2/12			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0012469	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000957	PMID:35979925	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0011265	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0011463	PMID:35979925	PCS		9/12			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000718	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000739	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000316	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000219	PMID:35979925	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0009765	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000455	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000750	PMID:35979925	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0002870	PMID:35979925	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000276	PMID:35979925	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000490	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0001263	PMID:35979925	PCS		5/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000294	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000729	PMID:35979925	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000508	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0001537	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000601	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0004209	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0007018	PMID:35979925	PCS		9/11			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0007359	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000201	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000960	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000347	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000545	PMID:35979925	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620782	Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder		HP:0000006	PMID:35979925	PCS					I	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0003577	OMIM:158310	TAS					C	HPO:skoehler[2012-10-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0007759	OMIM:158310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000365	PMID:31790666	PCS		0/7			P	HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0001596	PMID:31790666	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000221	PMID:31790666	PCS		7/7			P	HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0001096	PMID:31790666	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0002164	OMIM:158310	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0008070	PMID:31790666	PCS		7/7			P	HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0034418	PMID:31790666	PCS		7/7			P	HPO:probinson[2022-12-18]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000518	PMID:31790666	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0008396	OMIM:158310	IEA					P	HPO:iea[2009-02-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000639	OMIM:158310	IEA					P	HPO:iea[2009-02-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000618	OMIM:158310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000613	PMID:31790666	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0006552	OMIM:158310	IEA					P	HPO:iea[2009-02-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0001648	OMIM:158310	IEA					P	HPO:iea[2009-02-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0006532	OMIM:158310	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0007502	PMID:31790666	PCS		7/7			P	HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0009926	OMIM:158310	TAS					P	HPO:skoehler[2017-07-13]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0001880	OMIM:158310	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0031417	OMIM:158310	IEA					P	HPO:skoehler[2019-04-18]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000790	OMIM:158310	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0002090	OMIM:158310	IEA					P	HPO:skoehler[2010-06-20]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0032152	PMID:31790666	PCS		7/7			P	HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0011496	OMIM:158310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0002728	OMIM:158310	IEA					P	HPO:iea[2009-02-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0002208	PMID:31790666	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000565	OMIM:158310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0002249	OMIM:158310	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0008404	OMIM:158310	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0000006	PMID:31790666	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-10]
OMIM:158310	Mucoepithelial dysplasia, hereditary		HP:0002028	OMIM:158310	TAS		HP:0040283			P	HPO:skoehler[2013-05-29]
OMIM:234500	Hartnup disorder		HP:0001276	OMIM:234500	TAS					P	HPO:probinson[2009-02-17]
OMIM:234500	Hartnup disorder		HP:0000750	PMID:20399395	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0000992	PMID:20399395	PCS		1/1			P	HPO:skoehler[2015-02-01];HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0004322	OMIM:234500	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:234500	Hartnup disorder		HP:0001250	OMIM:234500	TAS					P	HPO:probinson[2009-02-17]
OMIM:234500	Hartnup disorder		HP:0002131	OMIM:234500	TAS					P	HPO:skoehler[2015-01-04]
OMIM:234500	Hartnup disorder		HP:0001263	OMIM:234500	TAS					P	HPO:probinson[2009-02-17]
OMIM:234500	Hartnup disorder		HP:0010818	PMID:20399395	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:6000332	PMID:4228120	PCS		2/2			P	HPO:probinson[2024-02-27]
OMIM:234500	Hartnup disorder		HP:0000709	OMIM:234500	TAS					P	HPO:probinson[2009-02-17]
OMIM:234500	Hartnup disorder		HP:0011463	PMID:20399395	PCS		1/1			C	HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0008353	PMID:20399395	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0000206	OMIM:234500	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:234500	Hartnup disorder		HP:0000712	OMIM:234500	TAS					P	HPO:probinson[2009-02-17]
OMIM:234500	Hartnup disorder		HP:0000007	PMID:15286787	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0000752	PMID:20399395	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0007018	PMID:20399395	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0001249	PMID:20399395	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:234500	Hartnup disorder		HP:0001347	OMIM:234500	TAS					P	HPO:probinson[2009-02-17]
OMIM:609310	Colorectal cancer, hereditary nonpolyposis, type 2		HP:0003003	PMID:8145827	PCS					P	HPO:probinson[2013-03-26];HPO:probinson[2020-07-20]
OMIM:609310	Colorectal cancer, hereditary nonpolyposis, type 2		HP:0000006	PMID:8145827	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0002069	PMID:24782409;PMID:30800706	PCS		5/5			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-05-10];HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0002344	PMID:24782409	PCS		4/4			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0003676	PMID:24782409	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0000750	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0002078	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0001266	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0001288	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0001272	PMID:24782409	PCS		4/4			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0001260	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0001263	PMID:24782409;PMID:30800706	PCS		5/5			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0003593	PMID:30800706	PCS		1/1			C	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0010852	PMID:24782409	PCS		2/4			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0002070	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0034360	PMID:24782409;PMID:30800706	PCS		5/5			P	HPO:probinson[2022-09-05]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0000639	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0000726	PMID:24782409	PCS		4/4			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0007366	PMID:24782409;PMID:30800706	PCS		5/5			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0000007	PMID:24782409	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0002527	PMID:30800706	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0001249	OMIM:616230	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616230	Epilepsy, progressive myoclonic, 8		HP:0001336	PMID:24782409;PMID:30800706	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-10];HPO:probinson[2022-05-10]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0006989	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0003577	PMID:32822602	PCS					C	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000486	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000540	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0001250	PMID:32822602	PCS		3/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0001272	PMID:32822602	PCS		2/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000085	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0025161	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0100333	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0012368	PMID:32822602	PCS		2/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0001629	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000733	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000414	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000179	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000311	PMID:32822602	PCS		2/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000176	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000154	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000252	PMID:32822602	PCS		2/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000010	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000076	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000494	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0001263	PMID:32822602	PCS		3/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0005164	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0011225	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0011003	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0005280	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0100334	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0012168	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0032471	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0001338	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0007874	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0007018	PMID:32822602	PCS		2/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000047	PMID:32822602	PCS		1/2	MALE		P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000006	PMID:32822602	PCS					I	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000028	PMID:32822602	PCS		2/2	MALE		P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000303	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0000369	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:619103	Neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities		HP:0005338	PMID:32822602	PCS		1/3			P	HPO:probinson[2021-02-14]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001298	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0002069	PMID:18513682	PCS		1/1			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0003234	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001695	PMID:18513682	PCS		1/1			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0003593	PMID:28857146	PCS		1/2			C	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0002240	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001508	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0000737	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001945	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0007325	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001522	PMID:18513682	PCS		1/1			C	HPO:skoehler[2019-02-15]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001942	OMIM:618235	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001249	PMID:28857146	PCS		1/1			P	HPO:probinson[2023-06-06];HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0003623	PMID:18513682	PCS		1/1			C	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001941	PMID:18513682	PCS		1/1			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0000252	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0002059	PMID:18513682	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0002013	PMID:18513682	PCS		1/1			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0002079	PMID:18513682	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0002376	PMID:28857146	PCS		2/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001662	PMID:18513682	PCS		1/1			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0011968	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001263	PMID:28857146;PMID:18513682	PCS		3/3			P	HPO:probinson[2023-06-06];HPO:probinson[2023-06-06];HPO:skoehler[2019-02-15]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0011923	PMID:28857146;PMID:18513682	PCS		3/3			P	HPO:probinson[2023-06-06];HPO:probinson[2023-06-06];HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0034295	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001639	PMID:18513682	PCS	HP:0003623	1/1			P	HPO:skoehler[2019-04-18]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0011153	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0000007	PMID:18513682	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001257	PMID:28857146	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0002104	PMID:18513682	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:618235	Mitochondrial complex I deficiency, nuclear type 13		HP:0001259	PMID:18513682	PCS		1/1			P	HPO:probinson[2023-06-06]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001276	OMIM:617106	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0002069	PMID:27476654	PCS		3/5			P	HPO:probinson[2023-03-07];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0003577	PMID:27476654	PCS		2/5			C	HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0002353	PMID:27476654	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0000486	PMID:27476654	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001371	OMIM:617106	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0002384	PMID:27476654	PCS		1/5			P	HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001263	PMID:27476654	PCS		5/5			P	HPO:skoehler[2017-07-13]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001251	PMID:27476654	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0003593	PMID:27476654	PCS		1/5			C	HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001290	OMIM:617106	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0032794	PMID:27476654	PCS		2/5			P	HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0000639	PMID:27476654	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0011167	PMID:27476654	PCS		1/5			P	HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0032660	PMID:27476654	PCS		4/5			P	HPO:probinson[2023-03-07];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0032792	PMID:27476654	PCS		1/5			P	HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0200134	PMID:27476654	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0000565	OMIM:617106	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0002305	PMID:27476654	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0000006	PMID:27476654	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001249	PMID:27476654	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001337	PMID:27476654	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0001347	OMIM:617106	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617106	Epileptic encephalopathy, early infantile, 42		HP:0003623	PMID:27476654	PCS		2/5			C	HPO:probinson[2023-03-07]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0002751	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0003510	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0003026	OMIM:184253	TAS					P	HPO:probinson[2015-02-22]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0001498	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0008839	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0003185	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0100255	OMIM:184253	TAS					P	HPO:probinson[2015-02-22]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0000907	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0000926	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0002938	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0002812	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0002834	PMID:23653587	PCS					P	HPO:probinson[2015-03-21]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0002857	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0006434	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0030292	PMID:23653587	PCS					P	HPO:probinson[2015-03-21]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0002657	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0000006	OMIM:184253	TAS					I	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0000545	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0001248	OMIM:184253	TAS					P	HPO:probinson[2009-02-17]
OMIM:184253	Spondylometaphyseal dysplasia, Algerian type		HP:0003865	OMIM:184253	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0002197	OMIM:601764	IEA					P	HPO:iea[2009-02-17]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0002384	OMIM:601764	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0002372	OMIM:601764	TAS					P	HPO:probinson[2009-02-17]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0003593	PMID:9147652	PCS					C	HPO:probinson[2024-03-10]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0007334	OMIM:601764	IEA					P	HPO:iea[2009-02-17]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0012759	PMID:9147652	PCS		0/25			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-10]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0000961	OMIM:601764	IEA					P	HPO:iea[2009-02-17]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0007359	PMID:9147652	PCS					P	HPO:probinson[2013-02-27];HPO:probinson[2024-03-10]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0000006	PMID:9147652	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-10]
OMIM:601764	Seizures, benign familial infantile, 1		HP:0002104	OMIM:601764	IEA					P	HPO:skoehler[2018-10-08]
OMIM:619895	Holoprosencephaly 14		HP:0001331	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0006988	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002069	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0009914	PMID:33820834	PCS		2/4			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000463	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001272	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000161	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0012806	PMID:33820834	PCS		2/4			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001290	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0410030	PMID:33820834	PCS		3/4			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002282	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0010883	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002280	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001629	PMID:33820834	PCS		2/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0007165	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0011461	PMID:33820834	PCS		4/4			C	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001305	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000238	PMID:33820834	PCS		3/4			P	HPO:probinson[2022-06-26];HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002416	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002119	PMID:33820834	PCS		2/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000256	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002951	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002410	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000175	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000252	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002353	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001360	PMID:33820834	PCS		3/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001263	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0032327	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0007291	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001719	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000007	PMID:33820834	PCS					I	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0001338	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0002007	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000400	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:619895	Holoprosencephaly 14		HP:0000369	PMID:33820834	PCS		1/4			P	HPO:probinson[2022-06-26]
OMIM:607473	Vitamin K-dependent clotting factors, combined deficiency of, 2		HP:0001892	OMIM:607473	TAS					P	HPO:probinson[2013-03-02]
OMIM:607473	Vitamin K-dependent clotting factors, combined deficiency of, 2		HP:0011858	OMIM:607473	TAS					P	HPO:probinson[2013-03-02]
OMIM:607473	Vitamin K-dependent clotting factors, combined deficiency of, 2		HP:0008321	OMIM:607473	TAS					P	HPO:probinson[2013-03-02]
OMIM:607473	Vitamin K-dependent clotting factors, combined deficiency of, 2		HP:0008169	OMIM:607473	TAS					P	HPO:probinson[2013-03-02]
OMIM:607473	Vitamin K-dependent clotting factors, combined deficiency of, 2		HP:0000007	PMID:11154138	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2019-01-21]
OMIM:607473	Vitamin K-dependent clotting factors, combined deficiency of, 2		HP:0040250	PMID:11154138	PCS					P	HPO:probinson[2019-01-21]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001276	PMID:35031858	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0004322	PMID:24721225	PCS		4/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001250	PMID:17989220;PMID:24721225	PCS		5/11			P	HPO:probinson[2013-02-17];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0002460	PMID:17989220	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0003593	PMID:35031858	PCS		1/1			C	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0011182	PMID:35031858	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0011167	PMID:35031858	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0000718	PMID:24721225	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0000717	PMID:17989220	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0002119	PMID:35031858	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0000256	PMID:17989220	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001249	PMID:17989220	PCS		8/8	MALE		P	HPO:probinson[2013-02-17];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0000336	PMID:24721225	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001347	PMID:35031858	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0200085	PMID:35031858	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001265	PMID:17989220	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0006913	PMID:35031858	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0000490	PMID:24721225	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001419	PMID:17989220	PCS					I	HPO:probinson[2013-01-09]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0000729	PMID:24721225	PCS		2/3			P	HPO:probinson[2020-08-03];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0100716	PMID:24721225	PCS		3/3			P	HPO:probinson[2020-08-03];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001533	PMID:17989220	PCS		6/8			P	HPO:probinson[2013-02-17]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0000248	PMID:24721225	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2020-08-03]
OMIM:300699	Intellectual developmental disorder, X-linked syndromic, Wu type		HP:0001336	PMID:17989220;PMID:35031858	PCS		3/9			P	HPO:probinson[2013-02-17];HPO:probinson[2022-05-10]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0001650	OMIM:617660	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000176	PMID:28792876	PCS		1/2			P	HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000252	PMID:28792876	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000076	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0003577	PMID:28792876	PCS		2/2			C	HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0001883	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0002144	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000376	PMID:28792876	PCS		1/2			P	HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0005950	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000089	PMID:28792876	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0004322	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000193	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0001263	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0004383	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0010301	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0010305	PMID:28792876;OMIM:617660	PCS		11/12			P	HPO:probinson[2022-08-23];HPO:skoehler[2018-10-08]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0012821	PMID:28792876	PCS		1/2			P	HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000407	PMID:28792876	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0001718	OMIM:617660	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0000007	PMID:28792876	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0003316	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0001631	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0001249	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617660	Vertebral, cardiac, renal, and limb defects syndrome 1		HP:0001601	PMID:28792876	PCS		1/2			P	HPO:probinson[2022-08-23]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0001760	PMID:21480433	PCS		10/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0011808	PMID:21480433	PCS		2/15			P	HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0003621	PMID:21480433	PCS		15/15			C	HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0003676	PMID:21480433	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0000365	PMID:21480433	PCS		4/11			P	HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0003693	PMID:21480433	PCS		15/15			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0002460	PMID:21480433	PCS		15/15			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0033685	PMID:21480433	PCS		2/2			P	HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0008180	PMID:21480433	PCS		4/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0001609	PMID:21480433	PCS		8/15			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0009830	PMID:21480433	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0002936	PMID:21480433	PCS		1/15			P	HPO:probinson[2022-10-31];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0000006	PMID:21480433	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0001337	PMID:21480433	PCS		3/15			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-31]
OMIM:614369	Peripheral neuropathy, myopathy, hoarseness, and hearing loss		HP:0006844	PMID:21480433	PCS		7/15			P	HPO:probinson[2022-10-31]
OMIM:613406	Witteveen-Kolk syndrome		HP:0006989	PMID:27399968	PCS		6/23			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000365	PMID:27399968	PCS		4/13			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000486	PMID:19233321	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0004322	PMID:33437032;PMID:27399968	PCS		13/42			P	HPO:probinson[2022-08-27];HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0003196	PMID:27399968	PCS		1/11			P	HPO:skoehler[2013-08-10];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002020	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0003593	PMID:30267900;PMID:19233321;PMID:27399968	PCS		8/12			C	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0012745	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0040262	PMID:27399968	PCS		2/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0012741	PMID:19233321	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0033052	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000518	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000639	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002539	PMID:27399968	PCS		3/12			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001845	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009466	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009623	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000752	PMID:19233321	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0003745	PMID:20678247	PCS					I	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002019	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0003623	PMID:27399968	PCS		1/10			C	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002311	PMID:30267900	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000494	PMID:30267900;PMID:19233321;PMID:27399968	PCS		11/13			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000252	PMID:33437032;PMID:27399968	PCS		19/41			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000490	PMID:27399968	PCS		2/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0100024	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000407	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0025646	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002705	OMIM:613406	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613406	Witteveen-Kolk syndrome		HP:0004209	PMID:30267900;PMID:27399968	PCS		5/12			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000400	PMID:19233321;PMID:27399968	PCS		2/12			P	HPO:probinson[2022-08-27];HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000006	PMID:27399968	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0003577	PMID:27399968	PCS		2/11			C	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001795	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000343	PMID:19233321	PCS		1/1			P	HPO:iea[2012-05-01];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000463	PMID:27399968	PCS		1/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001156	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001270	PMID:33437032;PMID:27399968	PCS		15/32			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000739	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000337	PMID:27399968	PCS		4/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0008872	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000612	PMID:33437032	PCS		1/28			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000219	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002119	PMID:27399968	PCS		3/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0030084	PMID:27399968	PCS		2/10			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000218	PMID:19233321;PMID:27399968	PCS		2/12			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000454	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000179	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001166	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001561	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000750	PMID:33437032;PMID:30267900	PCS		12/29			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002650	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0004279	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002376	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000194	OMIM:613406	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613406	Witteveen-Kolk syndrome		HP:0010535	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009275	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009795	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000348	PMID:19233321;PMID:27399968	PCS		3/12			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002007	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0007018	OMIM:613406	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000586	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000286	PMID:27399968	PCS		5/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001770	PMID:27399968	PCS		1/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002188	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001773	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001250	PMID:33437032;PMID:27399968	PCS		7/40			P	HPO:probinson[2022-08-27];HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000160	PMID:27399968	PCS		3/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001252	PMID:33437032;PMID:19233321;PMID:27399968	PCS		16/40			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001808	PMID:27399968	PCS		1/9			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0011463	PMID:27399968	PCS		1/10			C	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000319	PMID:27399968	PCS		2/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000718	PMID:19233321	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0011220	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000717	PMID:30267900;PMID:27399968	PCS		7/12			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000316	PMID:19233321	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0030260	OMIM:613406	TAS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001249	PMID:33437032;PMID:30267900	PCS		17/29			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002750	PMID:27399968	PCS		2/10			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002079	OMIM:613406	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613406	Witteveen-Kolk syndrome		HP:0011968	PMID:33437032;PMID:27399968	PCS		16/39			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001382	PMID:27399968	PCS		5/10			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001263	PMID:33437032;PMID:19233321;PMID:27399968	PCS		19/40			P	HPO:probinson[2022-08-27];HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0012378	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009890	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0034198	PMID:27399968	PCS		2/10			C	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000729	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000964	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000568	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000047	PMID:27399968	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000322	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009778	OMIM:613406	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613406	Witteveen-Kolk syndrome		HP:0005978	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000325	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000324	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000445	OMIM:613406	TAS					P	HPO:skoehler[2013-08-10]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009916	PMID:19921647;PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000540	PMID:27399968	PCS		3/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000023	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0010747	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0010862	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0011833	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000378	OMIM:613406	TAS					P	HPO:skoehler[2013-05-31]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000411	PMID:27399968	PCS		3/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001741	PMID:27399968	PCS		2/11			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000776	PMID:19233321	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000275	PMID:20678247	PCS					P	HPO:iea[2012-05-01]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002213	PMID:27399968	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000431	PMID:19233321	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000276	PMID:30267900;PMID:19233321	PCS		2/2			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000430	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000391	PMID:30267900;PMID:27399968	PCS		3/12			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0009909	PMID:27399968	PCS		2/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0002170	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0005280	PMID:30267900;PMID:27399968	PCS		3/12			P	HPO:probinson[2022-08-27];HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000308	OMIM:613406	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001518	OMIM:613406	TAS					P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0032077	PMID:27399968	PCS		1/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000426	PMID:27399968	PCS		1/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0430028	PMID:27399968	PCS		2/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000824	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0000307	PMID:27399968	PCS		7/11			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001511	PMID:27399968	PCS		1/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0200055	PMID:30267900;PMID:27399968	PCS		2/12			P	HPO:probinson[2022-08-27]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001510	PMID:20678247	PCS					P	HPO:iea[2012-04-24]
OMIM:613406	Witteveen-Kolk syndrome		HP:0001513	PMID:19233321	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-27]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:6000572	PMID:22386973	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0000750	OMIM:612718	TAS					P	HPO:probinson[2013-04-06]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0001992	OMIM:612718	TAS					P	HPO:skoehler[2013-09-10]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0001508	OMIM:612718	TAS					P	HPO:skoehler[2013-09-10]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0001263	OMIM:612718	TAS					P	HPO:probinson[2013-04-06]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0000717	OMIM:612718	TAS					P	HPO:probinson[2013-04-06]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0003593	OMIM:612718	TAS					C	HPO:skoehler[2013-09-10]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0000007	OMIM:612718	TAS					I	HPO:probinson[2013-04-06]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0003391	OMIM:612718	TAS		HP:0040283			P	HPO:skoehler[2013-09-10]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:6000748	PMID:20301745	PCS					P	HPO:probinson[2024-06-29]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0025051	PMID:20682460	PCS					P	HP:probinson[2019-01-27]
OMIM:612718	Cerebral creatine deficiency syndrome 3		HP:0001249	OMIM:612718	TAS					P	HPO:skoehler[2013-09-10]
OMIM:261515	D-bifunctional protein deficiency		HP:0000286	PMID:16278854	PCS		52/77			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0002069	PMID:9345094	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000486	PMID:16278854	PCS		40/73			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000365	PMID:16278854	PCS		29/64			P	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0005257	OMIM:261515	IEA					P	HPO:skoehler[2010-06-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001250	PMID:16278854	PCS	HP:0003623	79/85			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0003199	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0001252	PMID:9345094	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001171	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0033643	PMID:9345094	PCS		1/1			P	HPO:probinson[2021-04-16]
OMIM:261515	D-bifunctional protein deficiency		HP:0000639	PMID:16278854	PCS		40/73			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001408	PMID:16278854	PCS		2/23			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0002539	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0000316	PMID:16278854	PCS		52/77			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000239	PMID:16278854	PCS	HP:0003623				P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0006872	PMID:16278854	PCS		5/11			P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000278	PMID:16278854	PCS		52/77			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001765	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0003623	PMID:9345094	PCS		2/2			C	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000572	PMID:16278854	PCS		21/61			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0002750	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0002079	PMID:16278854	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001263	PMID:16278854	PCS		126/126			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0008167	PMID:9345094	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000767	PMID:9345094	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000007	PMID:16278854	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000762	PMID:16278854	PCS		16/24			P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000369	PMID:16278854	PCS		52/77			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0008207	PMID:9345094	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001397	PMID:16278854	IEA		5/23			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0030799	OMIM:261515;PMID:9345094	PCS		11/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001396	PMID:16278854	PCS		2/23			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000582	PMID:9345094	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000343	PMID:16278854	PCS		52/77			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001272	PMID:16278854	PCS		8/49			P	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001791	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0002240	PMID:16278854	PCS		32/73			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001508	PMID:16278854	PCS		27/61			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000938	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0007266	PMID:16278854	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0008872	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0002119	PMID:16278854	PCS		16/53			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000218	PMID:9345094	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0002832	PMID:16278854;PMID:9345094	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0002910	PMID:9345094	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000256	PMID:16278854	PCS		52/77			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001744	PMID:16278854	PCS		4/67			P	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000550	PMID:16278854	PCS		17/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001561	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0001762	PMID:9345094	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000270	PMID:9345094	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0002171	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0005280	PMID:9345094	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0007371	PMID:16278854	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0033044	PMID:16278854	PCS		7/61			P	HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000107	PMID:16278854	PCS		4/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000348	PMID:16278854	PCS		52/77			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0001319	PMID:16278854	PCS	HP:0003623	83/85			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000268	OMIM:261515	IEA					P	HPO:iea[2009-02-17]
OMIM:261515	D-bifunctional protein deficiency		HP:0002007	PMID:9345094	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0000347	PMID:9345094	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:261515	D-bifunctional protein deficiency		HP:0002126	PMID:16278854	PCS		7/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:613412	Esophagitis, eosinophilic, 2		HP:0100633	OMIM:613412	TAS					P	HPO:skoehler[2015-01-21]
OMIM:613412	Esophagitis, eosinophilic, 2		HP:0002015	OMIM:613412	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613412	Esophagitis, eosinophilic, 2		HP:0001880	OMIM:613412	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613412	Esophagitis, eosinophilic, 2		HP:0002013	OMIM:613412	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613412	Esophagitis, eosinophilic, 2		HP:0001508	OMIM:613412	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613412	Esophagitis, eosinophilic, 2		HP:0410019	OMIM:613412	TAS					P	HPO:skoehler[2017-07-13]
OMIM:182150	Simosa craniofacial syndrome		HP:0001595	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000343	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000023	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000364	OMIM:182150	TAS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-07]
OMIM:182150	Simosa craniofacial syndrome		HP:0000160	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000581	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0012368	OMIM:182150	TAS					P	HPO:skoehler[2017-07-13]
OMIM:182150	Simosa craniofacial syndrome		HP:0045075	OMIM:182150	TAS					P	HPO:probinson[2022-05-07]
OMIM:182150	Simosa craniofacial syndrome		HP:0000437	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000337	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000377	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000358	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000951	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0002553	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000431	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0003189	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000276	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000430	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000272	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0010751	OMIM:182150	TAS					P	HPO:skoehler[2013-05-31]
OMIM:182150	Simosa craniofacial syndrome		HP:0000506	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0002705	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000006	OMIM:182150	TAS					I	HPO:skoehler[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0000369	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:182150	Simosa craniofacial syndrome		HP:0001611	OMIM:182150	TAS		2/2			P	HPO:probinson[2009-02-17]
OMIM:300855	Ogden syndrome		HP:0004322	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0003196	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0010055	PMID:21700266	PCS		1/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0100807	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0008897	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0000113	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000494	PMID:21700266	PCS		3/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000252	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0000490	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001582	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0000492	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0033454	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000767	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000403	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000527	PMID:21700266	PCS		2/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0004969	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0004209	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000400	PMID:21700266	PCS		5/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001852	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000520	PMID:21700266	PCS		4/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000369	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0001276	PMID:21700266	PCS		2/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0003577	PMID:21700266	PCS		8/8			C	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000343	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000189	PMID:21700266	PCS		4/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002089	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002002	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0002000	PMID:21700266	PCS		1/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000737	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0031295	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000337	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000733	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0000219	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0002119	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000218	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0001423	OMIM:300855	TAS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:300855	Ogden syndrome		HP:0000454	PMID:21700266	PCS		3/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0006699	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0005989	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001664	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0004415	PMID:21700266	PCS		1/1			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000215	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0000456	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000973	PMID:21700266	PCS		3/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002014	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001562	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000473	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002015	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002650	PMID:21700266	PCS		1/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000233	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001684	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0010538	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002013	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0005487	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000470	PMID:21700266	PCS		3/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002092	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0011344	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002091	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0007495	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0006682	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0001558	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000348	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000105	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000347	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002069	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000286	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0000164	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0001374	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001891	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0010803	OMIM:300855	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300855	Ogden syndrome		HP:0025104	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001252	PMID:21700266	PCS		3/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0030939	OMIM:300855	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300855	Ogden syndrome		HP:0000280	PMID:21700266	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0045075	OMIM:300855	TAS					P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0011220	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0003828	OMIM:300855	TAS					M	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:300855	Ogden syndrome		HP:0001647	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000437	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000316	PMID:21700266	PCS		3/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0008734	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001643	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001488	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001004	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000952	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001403	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0004756	PMID:21700266	PCS		1/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0004755	PMID:21700266	PCS		2/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002750	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0011968	PMID:21700266	PCS		5/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002197	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001263	PMID:21700266	PCS		1/1		HP:0012828	P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0004491	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001419	PMID:21700266	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002904	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001537	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000964	PMID:21700266	PCS		4/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0003717	PMID:21700266	PCS		5/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000322	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002104	PMID:21700266	PCS		3/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001414	PMID:21700266	PCS		1/1			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001655	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0010508	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000023	PMID:21700266	PCS		3/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000260	PMID:21700266	PCS		5/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0011675	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0005272	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002719	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0001629	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0009762	PMID:21700266	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0011682	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002835	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0004737	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001901	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000411	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0009800	PMID:21700266	PCS		1/8			H	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001347	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002059	PMID:21700266	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0002213	OMIM:300855	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0000431	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0001640	PMID:21700266	PCS		3/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000034	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000430	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0000270	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0011823	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0005280	OMIM:300855	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300855	Ogden syndrome		HP:0100876	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0100598	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000308	PMID:21700266	PCS		3/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001511	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001631	OMIM:300855	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300855	Ogden syndrome		HP:0001510	PMID:21700266	PCS		2/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0001873	PMID:21700266	PCS		1/8			P	HPO:probinson[2022-05-08]
OMIM:300855	Ogden syndrome		HP:0000028	PMID:21700266	PCS		5/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2022-05-08]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0002069	PMID:34605855	PCS		3/8			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0002540	PMID:34605855	PCS		9/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0001696	PMID:34605855	PCS		1/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0002123	PMID:34605855	PCS		1/8			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0003593	PMID:34605855	PCS		8/10			C	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0002020	PMID:34605855	PCS		2/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0002240	PMID:34605855	PCS		1/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0010821	PMID:34605855	PCS		1/8			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0011463	PMID:34605855	PCS		1/10			C	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0012450	PMID:34605855	PCS		7/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0001249	PMID:34605855	PCS		10/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0003623	PMID:34605855	PCS		1/10			C	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0001347	PMID:34605855	PCS		4/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0008936	PMID:34605855	PCS		10/10			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0000252	PMID:34605855	PCS		8/10			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0001344	PMID:34605855	PCS		10/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0001263	PMID:34605855	PCS		10/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0032663	PMID:34605855	PCS		1/8			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0000708	PMID:34605855	PCS		6/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0032792	PMID:34605855	PCS		2/8			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0000007	PMID:34605855	PCS					I	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0000505	PMID:34605855	PCS		9/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0200134	PMID:34605855	PCS		5/10			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0007334	PMID:34605855	PCS		1/8			P	HPO:probinson[2022-08-13]
OMIM:619881	Developmental and epileptic encephalopathy 102		HP:0001631	PMID:34605855	PCS		1/10			P	HPO:probinson[2022-08-13]
OMIM:126180	Discrimination, two-point, reduction in		HP:0000707	OMIM:126180	IEA					P	HPO:iea[2009-02-17]
OMIM:126180	Discrimination, two-point, reduction in		HP:0000006	OMIM:126180	IEA					I	HPO:iea[2009-02-17]
OMIM:106250	Ankyloblepharon filiforme adnatum and cleft palate		HP:0000175	OMIM:106250	TAS					P	HPO:skoehler[2010-06-18]
OMIM:106250	Ankyloblepharon filiforme adnatum and cleft palate		HP:0009755	OMIM:106250	TAS					P	HPO:probinson[2013-02-24]
OMIM:106250	Ankyloblepharon filiforme adnatum and cleft palate		HP:0000006	OMIM:106250	TAS					I	HPO:probinson[2009-02-17]
OMIM:106250	Ankyloblepharon filiforme adnatum and cleft palate		HP:0000204	OMIM:106250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000286	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000483	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0004467	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000365	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000486	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0004322	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000463	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0001272	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0001251	PMID:30778173	PCS		3/4			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0012469	PMID:30778173	PCS	HP:0003593	2/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000639	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0100704	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0006970	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000414	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0002119	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000219	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0025336	PMID:30778173	PCS		4/6			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000510	PMID:30778173	PCS		3/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0008755	PMID:30778173	PCS	HP:0003577	2/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0001763	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0001249	PMID:30778173	PCS		5/5			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000473	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0005469	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0008936	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000750	PMID:30778173	PCS		4/5			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0002650	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0002079	PMID:30778173	PCS		6/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0031936	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0001283	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0011968	PMID:30778173	PCS		3/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0011947	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0001263	PMID:30778173	PCS		7/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0012799	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0002827	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0002509	PMID:30778173	PCS		2/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000648	PMID:30778173	PCS		4/7			P	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0002007	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000006	PMID:30778173	PCS					I	HPO:probinson[2020-07-01];HPO:probinson[2020-07-01]
OMIM:618547	Neurodevelopmental disorder with visual defects and brain anomalies		HP:0000687	PMID:30778173	PCS		1/7			P	HPO:probinson[2020-07-01]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0000286	PMID:27311568	PCS		2/10			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0000750	PMID:27311568	PCS		10/10			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0001382	PMID:27311568	PCS		3/10			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0002066	PMID:27311568	PCS		2/8			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0001263	PMID:25558065	PCS		1/1			P	HP:probinson[2019-02-02];HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0001252	PMID:27311568	PCS		2/10			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0001290	OMIM:618221	IEA					P	HPO:skoehler[2019-02-22]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0100962	PMID:27311568	PCS		2/8			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0000718	PMID:27311568	PCS		2/8			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0000729	PMID:27311568	PCS		2/8			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0001999	PMID:27311568	PCS		3/10			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0000007	PMID:27311568	PCS					I	HPO:probinson[2019-01-21];HPO:probinson[2019-01-21]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0007018	PMID:25558065	PCS		1/1			P	HP:probinson[2019-02-02]
OMIM:618221	Intellectual developmental disorder, autosomal recessive 66		HP:0001249	PMID:28097321;PMID:27311568;PMID:25558065	PCS		13/13			P	HP:probinson[2019-02-02]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0003676	PMID:20826435	PCS					C	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0000750	PMID:32450808	PCS		2/2			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0031936	PMID:20826435	PCS		3/3			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001250	PMID:20826435	PCS	HP:0003593	2/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001272	PMID:20826435	PCS	HP:0011462	1/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0002395	PMID:20826435;PMID:32450808	PCS		3/5			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001260	PMID:20826435	PCS		3/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001260	PMID:32450808	PCS	HP:0011463	2/2			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0002066	PMID:32450808	PCS		2/2			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001263	PMID:32450808	PCS		2/2			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001251	PMID:20826435	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0003593	PMID:20826435	PCS		2/3			C	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001152	PMID:32450808	PCS		3/4			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001270	PMID:20826435;PMID:32450808	PCS		5/5			P	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0000639	PMID:20826435	PCS		1/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0000007	PMID:20826435	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0002317	PMID:20826435	PCS		3/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0002317	PMID:32450808	PCS	HP:0011463	2/2			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0012391	PMID:20826435	PCS		3/3			P	HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0001249	PMID:20826435	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2020-09-15]
OMIM:615705	Spinocerebellar ataxia, autosomal recessive 15		HP:0002600	PMID:20826435	PCS		1/3			P	HPO:probinson[2020-09-15]
OMIM:165720	Osteoarthritis susceptibility 1		HP:0001426	PMID:15210948	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-07-17]
OMIM:165720	Osteoarthritis susceptibility 1		HP:0008843	PMID:15210948	PCS			FEMALE		P	HPO:iea[2009-02-17];HPO:probinson[2020-07-17]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0001265	OMIM:611588	IEA					P	HPO:skoehler[2010-06-18]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003323	PMID:17044012	PCS		1/3			P	HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003236	PMID:17044012	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003676	PMID:17044012	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0001762	OMIM:611588	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0001371	OMIM:611588	TAS					P	HPO:skoehler[2013-05-31]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0030046	PMID:17044012	PCS		3/3			P	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0011727	PMID:17044012	PCS		1/3			P	HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0001252	PMID:17044012	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003593	PMID:17044012	PCS		3/3			C	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003560	PMID:17044012	PCS		3/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0001270	PMID:17044012	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003391	OMIM:611588	IEA					P	HPO:skoehler[2010-06-18]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0009060	PMID:17044012	PCS		1/3			P	HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0008981	PMID:17044012	PCS		1/3			P	HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0000767	OMIM:611588	IEA					P	HPO:skoehler[2010-06-18]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0000007	PMID:17044012	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003307	OMIM:611588	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0002359	PMID:17044012	PCS		1/3			P	HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003701	PMID:17044012	PCS		3/3			P	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:611588	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4		HP:0003712	OMIM:611588	IEA					P	HPO:skoehler[2010-06-20]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0002373	PMID:34038384	PCS		23/33			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0002197	PMID:34038384	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0001250	PMID:34038384	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0011463	PMID:34038384	PCS		23/23			C	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0000729	PMID:34038384	PCS		1/34			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0007166	PMID:34038384	PCS		1/34			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0025190	PMID:34038384	PCS		3/34			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0033258	PMID:34038384	PCS		1/34			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0011170	PMID:34038384	PCS		2/34			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0007359	PMID:34038384	PCS		7/34			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620755	Generalized epilepsy with febrile seizures plus, type 12		HP:0000006	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:300100	Adrenoleukodystrophy		HP:0003455	OMIM:300100	TAS					P	HPO:probinson[2012-06-10]
OMIM:300100	Adrenoleukodystrophy		HP:0003676	OMIM:300100	TAS					C	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0000365	OMIM:300100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300100	Adrenoleukodystrophy		HP:0001596	PMID:24316281	IEA	HP:0003581				P	HPO:probinson[2019-05-22]
OMIM:300100	Adrenoleukodystrophy		HP:0001250	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0002385	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0001271	OMIM:300100	IEA					P	HPO:iea[2009-02-17]
OMIM:300100	Adrenoleukodystrophy		HP:0000020	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0001350	OMIM:300100	IEA					P	HPO:iea[2009-02-17]
OMIM:300100	Adrenoleukodystrophy		HP:0002180	OMIM:300100	TAS				HP:0003676	P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0007340	PMID:24316281	PCS	HP:0003581				P	HPO:probinson[2019-05-22]
OMIM:300100	Adrenoleukodystrophy		HP:0000618	OMIM:300100	IEA					P	HPO:iea[2009-02-17]
OMIM:300100	Adrenoleukodystrophy		HP:0002839	OMIM:300100	IEA					P	HPO:iea[2009-02-17]
OMIM:300100	Adrenoleukodystrophy		HP:0000953	OMIM:300100	IEA					P	HPO:iea[2009-02-17]
OMIM:300100	Adrenoleukodystrophy		HP:0000135	OMIM:300100	IEA					P	HPO:iea[2009-02-17]
OMIM:300100	Adrenoleukodystrophy		HP:0001268	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0002311	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0000572	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0002078	OMIM:300100	TAS					P	HPO:probinson[2012-06-10]
OMIM:300100	Adrenoleukodystrophy		HP:0001283	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0006938	PMID:24316281	PCS	HP:0003581				P	HPO:probinson[2019-05-22]
OMIM:300100	Adrenoleukodystrophy		HP:0002371	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0002070	OMIM:300100	TAS					P	HPO:probinson[2012-06-10]
OMIM:300100	Adrenoleukodystrophy		HP:0000709	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0000708	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0000726	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0001419	PMID:24316281	PCS					I	HPO:skoehler[2013-06-23];HPO:probinson[2019-05-22]
OMIM:300100	Adrenoleukodystrophy		HP:0002607	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0000802	PMID:24316281	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-05-22]
OMIM:300100	Adrenoleukodystrophy		HP:0001258	OMIM:300100	IEA					P	HPO:iea[2009-02-17]
OMIM:300100	Adrenoleukodystrophy		HP:0007018	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0002500	OMIM:300100	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300100	Adrenoleukodystrophy		HP:0008207	PMID:24316281	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-05-22]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0000253	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0008936	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0000252	PMID:28097321	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0001250	PMID:28097321	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0002187	PMID:26235277;PMID:28097321	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0001263	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0001252	PMID:28097321	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0003593	PMID:26235277	PCS		1/1			C	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0012389	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0032792	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0000007	PMID:26235277	PCS					I	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0000733	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0020221	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0008872	PMID:28097321	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0200134	PMID:26235277	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620033	Developmental and epileptic encephalopathy 107		HP:0000505	PMID:28097321	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0005588	OMIM:133200	TAS					P	HPO:iea[2009-02-17]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0025114	OMIM:133200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0005595	PMID:21879244	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0003593	OMIM:133200	TAS					C	HPO:iea[2009-02-17]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0025092	OMIM:133200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0000007	PMID:12019212	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-02]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0001019	PMID:21879244	IEA		1/1			P	HPO:probinson[2021-05-02]
OMIM:133200	Erythrokeratodermia variabilis et progressiva 1		HP:0000006	PMID:9843209	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:304400	Deafness, X-linked 2		HP:0000408	OMIM:304400	TAS					P	HPO:probinson[2012-07-16]
OMIM:304400	Deafness, X-linked 2		HP:0000381	OMIM:304400	TAS					P	HPO:probinson[2012-07-16]
OMIM:304400	Deafness, X-linked 2		HP:0001419	PMID:7839145	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-06-28]
OMIM:304400	Deafness, X-linked 2		HP:0000405	OMIM:304400	TAS					P	HPO:iea[2009-02-17]
OMIM:304400	Deafness, X-linked 2		HP:0000410	PMID:30176854	PCS		3/8			P	HPO:probinson[2021-06-28]
OMIM:304400	Deafness, X-linked 2		HP:0008527	PMID:30176854	PCS		3/8			P	HPO:probinson[2021-06-28];HPO:probinson[2021-06-28]
OMIM:304400	Deafness, X-linked 2		HP:0004458	PMID:30176854	PCS		4/4			P	HPO:probinson[2012-07-16];HPO:probinson[2021-06-28]
OMIM:604185	Facial paresis, hereditary congenital, 2		HP:0010628	OMIM:604185	IEA					P	HPO:iea[2009-02-17]
OMIM:604185	Facial paresis, hereditary congenital, 2		HP:0000365	OMIM:604185	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604185	Facial paresis, hereditary congenital, 2		HP:0003680	OMIM:604185	IEA					C	HPO:iea[2009-02-17]
OMIM:604185	Facial paresis, hereditary congenital, 2		HP:0000006	OMIM:604185	IEA					I	HPO:iea[2009-02-17]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0002630	OMIM:200100	PCS					P	HPO:probinson[2012-04-11]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0011096	OMIM:200100	PCS					P	HPO:probinson[2012-04-11]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0001927	OMIM:200100	PCS					P	HPO:probinson[2012-04-11]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0001251	OMIM:200100	PCS					P	HPO:probinson[2012-04-11]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0000007	OMIM:200100	PCS					I	HPO:probinson[2012-04-11]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0000546	PMID:24288038	PCS					P	HPO:probinson[2017-12-22]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0000488	OMIM:200100	TAS					P	HPO:skoehler[2015-07-26]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0007305	OMIM:200100	PCS					P	HPO:probinson[2012-04-11]
OMIM:200100	ABETALIPOPROTEINEMIA		HP:0008181	OMIM:200100	PCS					P	HPO:probinson[2012-04-11]
OMIM:607498	Migraine with or without aura, susceptibility to, 3		HP:0002013	OMIM:607498	IEA					P	HPO:iea[2009-02-17]
OMIM:607498	Migraine with or without aura, susceptibility to, 3		HP:0002077	OMIM:607498	IEA					P	HPO:iea[2009-02-17]
OMIM:607498	Migraine with or without aura, susceptibility to, 3		HP:0000613	OMIM:607498	IEA					P	HPO:iea[2009-02-17]
OMIM:607498	Migraine with or without aura, susceptibility to, 3		HP:0002083	OMIM:607498	IEA					P	HPO:iea[2009-02-17]
OMIM:607498	Migraine with or without aura, susceptibility to, 3		HP:0002183	OMIM:607498	IEA					P	HPO:iea[2009-02-17]
OMIM:607498	Migraine with or without aura, susceptibility to, 3		HP:0002018	OMIM:607498	IEA					P	HPO:iea[2009-02-17]
OMIM:607498	Migraine with or without aura, susceptibility to, 3		HP:0000006	OMIM:607498	IEA					I	HPO:iea[2009-02-17]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002883	OMIM:300672	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002521	PMID:15492925	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002540	OMIM:300672	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001773	PMID:15492925	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0000463	OMIM:300672	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002123	PMID:15492925	PCS		3/5			P	HPO:skoehler[2013-06-23];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001250	PMID:15492925	PCS		3/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001252	OMIM:300672	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002020	PMID:15492925	PCS		1/5			P	HPO:skoehler[2013-06-23];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0003593	PMID:15492925	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001290	PMID:15492925	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0010845	PMID:22264704	PCS		6/6			P	HP:probinson[2018-05-13]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0012469	PMID:15492925	PCS		3/5			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0100704	PMID:22264704	PCS					P	HP:probinson[2018-05-13]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0000817	PMID:15492925	PCS		2/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0011220	OMIM:300672	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0000337	OMIM:300672	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0000733	PMID:15492925	PCS		3/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001423	PMID:15492925	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002019	PMID:15492925	PCS		3/5			P	HPO:skoehler[2013-06-23];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0000179	OMIM:300672	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0000253	OMIM:300672	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002650	PMID:15492925	PCS		4/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002376	OMIM:300672	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0002197	PMID:15492925	PCS		3/5			P	HPO:skoehler[2013-06-23];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0000490	OMIM:300672	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001263	PMID:15492925	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001182	OMIM:300672	TAS					P	HPO:skoehler[2013-06-23]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0031165	OMIM:300672	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0200134	PMID:15492925	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0200055	PMID:15492925	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-25]
OMIM:300672	Developmental and epileptic encephalopathy 2		HP:0001336	PMID:15492925	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0002465	PMID:30167849	PCS		1/2			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0000252	PMID:35298461	PCS		7/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0000582	PMID:35298461	PCS					P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0000750	PMID:35298461	PCS		8/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0001344	PMID:35298461	PCS		3/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0031936	PMID:35298461	PCS		8/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0004322	PMID:35298461	PCS					P	HPO:probinson[2022-10-05];HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0001250	PMID:35298461	PCS		4/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0001263	PMID:35298461	PCS		8/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0001252	PMID:35298461	PCS		8/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0010864	PMID:35298461;PMID:30167849	PCS		10/10			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0011463	PMID:35298461	PCS		8/8			C	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0000718	PMID:30167849	PCS		1/2			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0000007	PMID:30167849	PCS					I	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0002515	PMID:35298461	PCS		3/8			P	HPO:probinson[2022-10-05]
OMIM:620027	Neurodevelopmental disorder with microcephaly, short stature, and speech delay		HP:0000664	PMID:35298461	PCS					P	HPO:probinson[2022-10-05]
OMIM:300114	Raynaud-Claes syndrome		HP:0000486	OMIM:300114	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300114	Raynaud-Claes syndrome		HP:0001332	PMID:23647072	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0001250	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0002384	PMID:23647072	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0002120	OMIM:300114	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0001252	PMID:23647072	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0003593	PMID:23647072	PCS		1/1			C	HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0002061	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0001290	OMIM:300114	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300114	Raynaud-Claes syndrome		HP:0000280	OMIM:300114	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300114	Raynaud-Claes syndrome		HP:0000716	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0100704	OMIM:300114	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0000718	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0000739	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0007302	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0001423	PMID:23647072	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0000252	PMID:23647072	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0000494	OMIM:300114	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0002059	OMIM:300114	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0002650	OMIM:300114	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300114	Raynaud-Claes syndrome		HP:0001344	OMIM:300114	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300114	Raynaud-Claes syndrome		HP:0000276	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0002079	PMID:23647072	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0001263	PMID:23647072	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0002073	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0011800	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0000708	OMIM:300114	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300114	Raynaud-Claes syndrome		HP:0000729	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0000722	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300114	Raynaud-Claes syndrome		HP:0200134	PMID:23647072	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-11-25]
OMIM:300114	Raynaud-Claes syndrome		HP:0000303	OMIM:300114	IEA					P	HPO:skoehler[2019-02-22]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0002983	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000343	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0008905	PMID:12110406	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0004960	OMIM:610682	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000364	PMID:12110406	PCS		0/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0003179	PMID:12110406	PCS		4/8			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0004322	OMIM:610682	TAS					P	HPO:probinson[2009-02-17]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000260	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0030674	PMID:12110406	PCS		4/4			C	HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0005474	OMIM:610682	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000938	OMIM:610682	TAS					P	HPO:probinson[2009-02-17]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0002979	PMID:12110406	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0008796	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0002812	PMID:12110406	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0002757	PMID:12110406	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0001522	OMIM:610682	TAS					C	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000774	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0002953	PMID:12110406	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000311	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0001623	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0001249	PMID:12110406	PCS		0/8			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0005304	OMIM:610682	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0002650	PMID:12110406	PCS		4/5			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000270	OMIM:610682	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000592	PMID:12110406	PCS		8/8			P	HPO:probinson[2012-05-27];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0010537	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000767	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000007	OMIM:610682	TAS					I	HPO:probinson[2009-02-17]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0006640	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000703	PMID:12110406	PCS		0/8			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0006367	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0002645	PMID:12110406	PCS		2/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000520	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0000126	OMIM:610682	TAS					P	HPO:probinson[2012-05-27]
OMIM:610682	Osteogenesis imperfecta, type VII		HP:0005855	OMIM:610682	IEA		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-04]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0000695	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0001156	OMIM:601957	TAS					P	HPO:skoehler[2014-11-26]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0002164	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0001010	OMIM:601957	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0010719	OMIM:601957	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0010105	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0010034	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0012471	OMIM:601957	TAS					P	HPO:skoehler[2013-12-19]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0009882	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0000954	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0000689	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0006189	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0001857	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0008404	OMIM:601957	TAS					P	HPO:skoehler[2013-05-03]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0000006	OMIM:601957	IEA					I	HPO:iea[2009-02-17]
OMIM:601957	Odontotrichoungual-Digital-Palmar syndrome		HP:0000303	OMIM:601957	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0001297	PMID:16864835	PCS		7/9			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0003596	PMID:10371078;PMID:16864835	PCS		5/8			C	HPO:probinson[2022-07-01];HPO:probinson[2022-04-24]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0001250	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000020	PMID:16864835	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0012671	PMID:10371078	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0011462	PMID:16864835	PCS		3/7			C	HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0002619	PMID:16864835	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0007123	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0007024	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0001269	PMID:16864835	PCS		5/9			P	HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000751	PMID:10371078	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000512	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000572	OMIM:125310	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0002354	PMID:10371078	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0001288	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0030223	PMID:10371078	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0002076	PMID:16864835	PCS		6/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0002352	PMID:10371078	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0032325	PMID:16864835	PCS		7/9			P	HPO:probinson[2022-07-01]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000709	PMID:10371078	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000708	OMIM:125310	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-05]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000726	PMID:10371078;PMID:16864835	PCS		5/10			P	HPO:probinson[2022-07-01];HPO:probinson[2022-04-24]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000649	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0009830	OMIM:125310	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0007236	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0003657	PMID:10371078	PCS					P	HPO:probinson[2022-09-05]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0007634	OMIM:125310	IEA					P	HPO:iea[2009-02-17]
OMIM:125310	Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy		HP:0000006	PMID:8878478	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:615922	Retinitis pigmentosa 70		HP:0001133	PMID:24419317	PCS		4/5			P	HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0003621	PMID:24419317	PCS		1/4			C	HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0000662	PMID:24419317	PCS		4/5			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0011462	PMID:24419317	PCS		3/4			C	HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0000608	PMID:24419317	PCS		4/5			P	HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0000546	PMID:24419317	PCS		5/5			P	HPO:skoehler[2014-10-17];HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0007663	PMID:24419317	PCS		5/5			P	HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0000543	PMID:24419317	PCS		4/5			P	HPO:skoehler[2014-10-17];HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0000510	PMID:24419317	PCS		5/5			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0007843	PMID:24419317	PCS		4/5			P	HPO:probinson[2023-01-26]
OMIM:615922	Retinitis pigmentosa 70		HP:0000006	PMID:24419317	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-26]
OMIM:249500	Intellectual developmental disorder, autosomal recessive 1		HP:0006801	OMIM:249500	TAS					P	HPO:probinson[2012-09-16]
OMIM:249500	Intellectual developmental disorder, autosomal recessive 1		HP:0000486	OMIM:249500	IEA					P	HPO:iea[2009-02-17]
OMIM:249500	Intellectual developmental disorder, autosomal recessive 1		HP:0003487	OMIM:249500	TAS					P	HPO:probinson[2012-09-16]
OMIM:249500	Intellectual developmental disorder, autosomal recessive 1		HP:0000639	OMIM:249500	IEA					P	HPO:iea[2009-02-17]
OMIM:249500	Intellectual developmental disorder, autosomal recessive 1		HP:0011463	PMID:12459588	PCS		5/5			C	HPO:probinson[2022-06-16];HPO:probinson[2022-06-16]
OMIM:249500	Intellectual developmental disorder, autosomal recessive 1		HP:0002151	PMID:12459588	PCS		0/4			P	HPO:probinson[2022-06-16]
OMIM:249500	Intellectual developmental disorder, autosomal recessive 1		HP:0000007	PMID:12459588	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-16]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001650	OMIM:143095	TAS				HP:0012825	P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002982	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000684	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000365	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0004322	PMID:18513679;PMID:15215498	PCS		15/15			P	HPO:probinson[2012-05-27];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001371	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0100490	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001373	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003031	OMIM:143095	TAS				HP:0012840	P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003593	PMID:15215498	PCS		9/9			C	HPO:probinson[2024-03-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0010049	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003071	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0045075	OMIM:143095	TAS					P	HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0010446	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000914	OMIM:143095	TAS					P	HPO:skoehler[2015-12-30]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0006471	OMIM:143095	TAS					P	HPO:skoehler[2013-01-22]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0008450	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002816	PMID:18513679	PCS		3/6			P	HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002938	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000316	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002857	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001763	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001642	OMIM:143095	TAS				HP:0012825	P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001249	PMID:15215498	PCS		0/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002655	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002553	OMIM:143095	TAS		HP:0040282			P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002751	OMIM:143095	TAS				HP:0012828	P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002750	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003042	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000691	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003040	OMIM:143095	TAS					P	HPO:skoehler[2013-01-22]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002194	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003083	PMID:18513679	PCS		6/6			P	HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0005180	OMIM:143095	TAS				HP:0012826	P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002829	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0009179	OMIM:143095	TAS					P	HPO:skoehler[2013-01-22]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0006462	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0006067	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000007	PMID:15215498	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0007598	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001659	OMIM:143095	TAS				HP:0012826	P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002945	PMID:15215498	PCS		9/9			P	HPO:probinson[2012-05-27];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001653	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003834	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000687	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003577	PMID:18513679	PCS		6/6			C	HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000343	OMIM:143095	TAS		HP:0040282			P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0008905	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001552	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001156	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:6000970	PMID:18513679	PCS		2/2			P	HPO:probinson[2024-08-04]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003093	PMID:15215498	PCS		9/9			P	HPO:probinson[2012-05-28];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0010585	PMID:15215498	PCS		9/9			P	HPO:probinson[2012-05-27];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003090	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0100864	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001629	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0008551	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0009882	OMIM:143095	TAS					P	HPO:skoehler[2012-10-17]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000337	OMIM:143095	TAS		HP:0040282			P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002515	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000218	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0006610	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0004976	PMID:18513679	PCS	HP:0003577	6/6			P	HPO:probinson[2012-05-27];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0009803	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001623	PMID:18513679	PCS		3/6			P	HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003301	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002650	PMID:15215498	PCS		9/9			P	HPO:probinson[2012-05-27];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001762	PMID:18513679	PCS	HP:0003577	6/6			P	HPO:probinson[2012-05-27];HPO:probinson[2022-05-08]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003022	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0000470	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003184	OMIM:143095	TAS					P	HPO:skoehler[2013-01-22]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002092	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002808	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001718	OMIM:143095	TAS				HP:0012828	P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0003417	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0002967	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:143095	Spondyloepiphyseal dysplasia with congenital joint dislocations		HP:0001714	OMIM:143095	TAS					P	HPO:probinson[2012-05-27]
OMIM:612095	Retinitis pigmentosa 41		HP:0000550	PMID:10587575	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0007737	PMID:17605048	PCS		6/6			P	HPO:probinson[2021-05-12];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0000662	PMID:10587575	PCS	HP:0011463				P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0001141	PMID:10587575;PMID:17605048	PCS		16/16			P	HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0000580	PMID:10587575	PCS					P	HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0000639	PMID:17605048	PCS		5/6			P	HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0011463	PMID:17605048	PCS		5/5			C	HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0000608	PMID:17605048	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-12];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0000007	PMID:10587575	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0007994	PMID:10587575	PCS	HP:0011463				P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0000510	PMID:10587575	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0000543	PMID:10587575;PMID:17605048	PCS		16/16			P	HPO:probinson[2021-05-12];HPO:probinson[2021-05-12];HPO:probinson[2021-05-12]
OMIM:612095	Retinitis pigmentosa 41		HP:0007843	PMID:10587575;PMID:17605048	PCS		16/16			P	HPO:probinson[2021-05-12];HPO:probinson[2021-05-12];HPO:probinson[2021-05-12]
OMIM:276900	Usher syndrome, type I		HP:0000572	OMIM:276900	TAS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:276900	Usher syndrome, type I		HP:0000550	OMIM:276900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:276900	Usher syndrome, type I		HP:0000639	PMID:21436283	PCS		1/1			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:276900	Usher syndrome, type I		HP:0000407	PMID:21436283	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:276900	Usher syndrome, type I		HP:0003593	PMID:21436283	PCS		1/1			C	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:276900	Usher syndrome, type I		HP:0000007	PMID:7870171	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-02]
OMIM:276900	Usher syndrome, type I		HP:0001270	OMIM:276900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:276900	Usher syndrome, type I		HP:0008555	OMIM:276900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:276900	Usher syndrome, type I		HP:0000510	PMID:21436283	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-02]
OMIM:276900	Usher syndrome, type I		HP:0000512	PMID:21436283	PCS		1/1			P	HPO:probinson[2022-09-02];HPO:probinson[2022-09-02]
OMIM:201550	Adducted thumbs syndrome		HP:0000220	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0002058	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0000175	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0000252	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0001363	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0002015	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0003198	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0001290	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0002093	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0006990	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0000998	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0007266	OMIM:201550	PCS					P	HPO:probinson[2012-03-12]
OMIM:201550	Adducted thumbs syndrome		HP:0000007	OMIM:201550	IEA					I	HPO:iea[2009-02-17]
OMIM:201550	Adducted thumbs syndrome		HP:0002804	OMIM:201550	IEA					P	HPO:skoehler[2015-01-19]
OMIM:201550	Adducted thumbs syndrome		HP:0002705	OMIM:201550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:201550	Adducted thumbs syndrome		HP:0000218	OMIM:201550	IEA					P	HPO:iea[2009-02-17]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000286	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0002188	PMID:31353022	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000486	PMID:31353022	PCS		5/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0001250	PMID:31353022	PCS		5/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0003155	PMID:31353022	PCS		0/5			P	HPO:probinson[2020-07-24];HPO:probinson[2024-03-16]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0001252	PMID:31353022	PCS		5/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0003196	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000639	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000319	PMID:31353022	PCS		5/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000998	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000238	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000358	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0003623	PMID:31353022	PCS					C	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0002079	PMID:31353022	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0001382	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000490	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0012736	PMID:31353022	PCS		4/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000767	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000007	PMID:31353022	PCS					I	HPO:probinson[2020-12-04]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000648	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0001257	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000369	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000341	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000540	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0001272	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0011712	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0002280	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0002719	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0100704	PMID:31353022	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000938	PMID:31353022	PCS		1/1			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000337	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000219	PMID:31353022	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0002714	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000218	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0001320	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000154	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0002059	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0003189	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0002650	PMID:31353022	PCS		5/5		HP:0012828	P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0001321	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000276	PMID:31353022	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0003100	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000272	PMID:31353022	PCS		5/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0011344	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0005280	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0011471	PMID:31353022	PCS		2/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000506	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000348	PMID:31353022	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618590	Neurodevelopmental disorder with brain anomalies, seizures, and scoliosis		HP:0000307	PMID:31353022	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:178995	Pruritic urticarial papules and plaques of pregnancy		HP:0001065	OMIM:178995	IEA					P	HPO:skoehler[2010-06-20]
OMIM:178995	Pruritic urticarial papules and plaques of pregnancy		HP:0000006	OMIM:178995	IEA					I	HPO:iea[2009-02-17]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001770	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001773	PMID:22885700	IEA		3/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001377	PMID:22885700	IEA		4/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000365	OMIM:300882	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0004322	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001250	PMID:22885700	IEA					P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0002020	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001290	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0003828	OMIM:300882	TAS					M	HPO:skoehler[2015-12-30]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000316	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0009623	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0008897	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0008734	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000278	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001007	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001249	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0002553	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000175	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000054	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000252	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0003764	OMIM:300882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000490	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001263	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000294	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000965	PMID:22885700	IEA		2/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000527	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001417	PMID:22885700	IEA					I	HPO:probinson[2013-01-09]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0004209	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000248	PMID:22885700	IEA		3/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000687	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000343	PMID:22885700	IEA		4/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000463	PMID:22885700	IEA		2/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0040082	OMIM:300882	TAS					P	HPO:skoehler[2014-11-27]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0008872	PMID:22885700	IEA		2/4			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0002119	PMID:22885700	IEA		3/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0002714	PMID:22885700	IEA		4/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000218	PMID:22885700	IEA		3/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000455	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001423	OMIM:300882	TAS					I	HPO:skoehler[2015-12-30]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000135	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000233	PMID:22885700	IEA		4/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000470	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0005280	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000708	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000506	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000508	PMID:22885700	IEA		2/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000426	PMID:22885700	IEA		4/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0001956	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000664	PMID:22885700	IEA		5/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0200055	PMID:22885700	IEA		6/10			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000347	PMID:22885700	IEA		4/5			P	HPO:probinson[2013-03-23]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000545	OMIM:300882	TAS					P	HPO:skoehler[2014-10-06]
OMIM:300882	Cornelia de Lange syndrome 5		HP:0000028	OMIM:300882	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002421	PMID:24115232	PCS		2/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000286	PMID:24115232	PCS		2/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002521	PMID:24115232;PMID:23561849	PCS		4/6			P	HPO:probinson[2021-06-15];HPO:probinson[2021-06-15];HPO:skoehler[2013-06-04];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002188	PMID:34122512	PCS		1/4			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001250	PMID:23561849;PMID:34122512	PCS		6/7			P	HPO:probinson[2021-06-15];HPO:skoehler[2013-06-04];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002263	PMID:24115232	PCS		2/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001252	PMID:24115232;PMID:23561849;PMID:34122512	PCS		5/8			P	HPO:probinson[2021-06-15];HPO:skoehler[2014-11-26];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002020	OMIM:300896	TAS		HP:0040283			P	HPO:skoehler[2013-06-04]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000280	PMID:24115232	TAS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002280	PMID:34122512	PCS		1/4			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000639	OMIM:300896	TAS					P	HPO:skoehler[2013-06-04]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002719	OMIM:300896	TAS					P	HPO:skoehler[2013-06-04]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0012471	OMIM:300896	TAS					P	HPO:skoehler[2014-07-11]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0006297	PMID:24115232	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000218	PMID:24115232	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000510	OMIM:300896	TAS					P	HPO:skoehler[2013-06-04]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001423	PMID:34122512	PCS					I	HPO:skoehler[2013-06-04];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001249	PMID:34122512	PCS		3/4			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0003623	PMID:24115232	PCS		3/3			C	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001562	PMID:34122512	PCS		1/4			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002059	PMID:23561849	PCS		1/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000252	PMID:23561849	PCS		2/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0006956	PMID:34122512	PCS		1/4			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000574	PMID:24115232	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000431	PMID:24115232	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001344	PMID:24115232	PCS		3/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001586	PMID:24115232	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001321	PMID:23561849	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0002079	PMID:23561849	PCS		1/3			P	HPO:skoehler[2013-06-04];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001442	OMIM:300896	TAS					I	HPO:skoehler[2013-06-04]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000194	PMID:24115232	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000293	PMID:24115232	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0003265	PMID:34122512	PCS		3/4			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001263	PMID:23561849;PMID:34122512	PCS		6/7			P	HPO:probinson[2021-06-15];HPO:skoehler[2013-06-04];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000074	PMID:24115232	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0003160	PMID:23561849;PMID:34122512	PCS		4/7			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0031931	OMIM:300896	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0011097	PMID:24115232	PCS		3/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000822	PMID:23561849	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0200134	PMID:24115232	TAS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001511	PMID:34122512	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000322	PMID:24115232	PCS		2/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0001631	PMID:24115232	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0000303	PMID:24115232	PCS		3/3			P	HPO:probinson[2021-06-15]
OMIM:300896	Congenital disorder of glycosylation, type IIm		HP:0011090	PMID:24115232	PCS		1/3			P	HPO:probinson[2021-06-15]
OMIM:612917	Giacheti syndrome		HP:0000098	OMIM:612917	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612917	Giacheti syndrome		HP:0000276	OMIM:612917	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612917	Giacheti syndrome		HP:0002167	OMIM:612917	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612917	Giacheti syndrome		HP:0001328	OMIM:612917	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612917	Giacheti syndrome		HP:0000348	OMIM:612917	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612917	Giacheti syndrome		HP:0000601	OMIM:612917	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612917	Giacheti syndrome		HP:0001833	OMIM:612917	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612917	Giacheti syndrome		HP:0000006	OMIM:612917	IEA					I	HPO:skoehler[2010-06-19]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0003621	PMID:28386624	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002067	PMID:28386624	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002375	PMID:28386624	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002243	PMID:28386624	PCS		1/2			P	HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0003487	PMID:28386624	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002376	PMID:28386624	PCS	HP:0003621	2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002154	PMID:28386624	PCS		3/4			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002151	PMID:28386624	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002490	PMID:28386624	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0001270	PMID:28386624	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0040014	PMID:28386624	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0011463	PMID:28386624	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0000007	PMID:28386624	PCS					I	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0008347	PMID:28386624	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0003648	PMID:28386624	PCS					P	HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0002205	PMID:28386624	PCS		1/2			P	HPO:probinson[2020-12-08]
OMIM:619063	Mitochondrial complex IV deficiency, nuclear type 19		HP:0500233	PMID:28386624	PCS		1/1			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002168	PMID:26224725	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0001310	PMID:26224725	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0001272	PMID:23418007;PMID:26224725	PCS		7/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002066	PMID:23418007	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0001152	PMID:23418007	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0001251	PMID:23418007	PCS		6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0000639	PMID:26224725	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0011463	PMID:23418007;PMID:26224725	PCS		6/7			C	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0000657	PMID:26224725	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002317	PMID:26224725	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0001347	PMID:23418007	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002015	PMID:23418007	PCS		1/6			P	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002312	PMID:23418007	PCS		1/6			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0000651	PMID:23418007	PCS		1/6			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0000012	PMID:23418007	PCS		1/6			P	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0030147	PMID:26224725	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0003487	PMID:23418007	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002495	PMID:23418007	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0001260	PMID:23418007	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002174	PMID:23418007	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0002070	PMID:23418007	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0025708	PMID:23418007	PCS		1/6			C	HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0000007	PMID:23418007	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0003677	PMID:23418007	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:609270	Spinocerebellar ataxia, autosomal recessive 7		HP:0007338	PMID:23418007	PCS		1/6			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-09]
OMIM:147350	Incisors, rotation of upper central		HP:0006330	OMIM:147350	IEA					P	HPO:iea[2009-02-17]
OMIM:147350	Incisors, rotation of upper central		HP:0000006	OMIM:147350	IEA					I	HPO:iea[2009-02-17]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0002257	PMID:19200523;PMID:23993197	PCS		20/22			P	HPO:probinson[2022-05-15];HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0001696	PMID:23993197	PCS		0/12			P	HPO:probinson[2013-04-14];HPO:probinson[2022-05-15]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0004322	PMID:19200523	PCS					P	HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0002110	PMID:19200523;PMID:23993197	PCS		19/22			P	HPO:probinson[2022-05-15];HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0033036	PMID:23993197	PCS		4/5			P	HPO:probinson[2022-05-15]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0012207	PMID:23993197	PCS		1/1			P	HPO:probinson[2022-05-15]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0012208	PMID:19200523	PCS					P	HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0011109	PMID:19200523;PMID:23993197	PCS		20/22			P	HPO:probinson[2022-05-15];HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0012265	PMID:19200523	PCS					P	HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0012260	PMID:19200523	PCS					P	HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0011463	PMID:23993197	PCS		12/12			C	HPO:probinson[2022-05-15]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0000007	PMID:19200523	PCS					I	HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0006510	PMID:23993197	PCS		3/12			P	HPO:probinson[2022-05-15]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0002205	PMID:19200523	PCS					P	HPO:probinson[2013-04-14]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0000389	PMID:23993197	PCS		8/12			P	HPO:probinson[2022-05-15]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0002643	PMID:23993197	PCS	HP:0003623	4/12			P	HPO:probinson[2022-05-15]
OMIM:612650	Ciliary dyskinesia, primary, 12		HP:0003546	PMID:19200523	PCS					P	HPO:probinson[2013-04-14]
DECIPHER:43	7q11.23 duplication syndrome		HP:0000750	DECIPHER:43	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:43	7q11.23 duplication syndrome		HP:0000736	DECIPHER:43	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:43	7q11.23 duplication syndrome		HP:0001249	DECIPHER:43	IEA					P	HPO:skoehler[2013-05-29]
OMIM:620184	Atelis syndrome 1		HP:0001276	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000343	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001252	PMID:36333305	PCS		2/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0003593	PMID:36333305	PCS		7/7			C	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0040262	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000518	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000958	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0002719	PMID:36333305	PCS		2/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001629	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001903	PMID:36333305	PCS		2/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000957	PMID:36333305	PCS		3/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0008551	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0008454	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0007400	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000218	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000670	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000494	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001882	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000276	PMID:36333305	PCS		2/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000331	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0011968	PMID:36333305	PCS		3/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0002110	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001263	PMID:36333305	PCS		7/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0012366	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0031382	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000729	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000448	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000007	PMID:36333305	PCS					I	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000964	PMID:36333305	PCS		2/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0000821	PMID:36333305	PCS		2/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001319	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001631	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0007018	PMID:36333305	PCS		2/7			P	HPO:probinson[2023-06-11]
OMIM:620184	Atelis syndrome 1		HP:0001873	PMID:36333305	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:300909	Acquired angioedema		HP:0100665	OMIM:300909	IEA					P	HPO:skoehler[2015-01-19]
OMIM:616436	Epilepsy, familial temporal lobe, 7		HP:0003829	PMID:26046367	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-26]
OMIM:616436	Epilepsy, familial temporal lobe, 7		HP:0011158	PMID:26046367	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-26]
OMIM:616436	Epilepsy, familial temporal lobe, 7		HP:0000006	PMID:26046367	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-26]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0002850	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0002136	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0004432	PMID:32905580	PCS		3/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0100280	PMID:32905580	PCS		1/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0030388	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0002110	PMID:32905580	IEA		1/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0001263	PMID:32905580	PCS		1/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0005133	PMID:32905580	PCS		1/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0003593	PMID:32905580	PCS		3/3			C	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0033542	PMID:32905580	PCS		1/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0010862	PMID:32181500	PCS		3/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0002194	PMID:32181500	PCS		3/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0012389	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0010976	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0005180	PMID:32905580	PCS		1/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0001639	PMID:32181500;PMID:32905580	PCS		6/6			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0001716	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0030252	PMID:32905580	PCS		3/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0000007	PMID:32181500	PCS					I	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0004315	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:619705	Immunodeficiency 93 and hypertrophic cardiomyopathy		HP:0001875	PMID:32181500	PCS		2/3			P	HPO:probinson[2022-03-20]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0003565	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0003202	OMIM:606631	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0003155	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0003273	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0012514	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0006380	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0100774	OMIM:606631	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0001519	OMIM:606631	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0000938	OMIM:606631	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0002515	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0002944	OMIM:606631	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0000823	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0001324	PMID:11807860	PCS					P	HPO:probinson[2017-09-29]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0001653	OMIM:606631	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0000135	OMIM:606631	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0000006	OMIM:606631	TAS					I	HPO:skoehler[2017-07-13]
OMIM:606631	Camurati-engelmann disease, type 2		HP:0001634	OMIM:606631	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002168	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003431	PMID:12873855	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002166	PMID:12873855	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001310	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003693	OMIM:270550	TAS				HP:0012828	P	HPO:probinson[2012-04-25]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002460	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003593	PMID:12873855	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002064	PMID:18465152	PCS		13/13			P	HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001251	PMID:18465152	PCS		16/16			P	HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0007083	PMID:12873855	PCS		18/18			P	HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0006150	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:4000169	PMID:23497566	PCS		8/8			P	HPO:probinson[2023-03-31]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0000639	PMID:12873855	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0007240	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0007001	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0007221	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0009049	PMID:12873855	PCS	HP:0003581	18/18		HP:0012825	P	HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002936	OMIM:270550	TAS					P	HPO:probinson[2012-04-25]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003448	PMID:12873855	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001249	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0006855	PMID:18465152;PMID:12873855	PCS		22/22			P	HPO:probinson[2009-02-17];HPO:probinson[2020-02-02];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001765	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0007922	PMID:12873855	PCS		2/18			P	HPO:probinson[2015-07-19];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001347	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003387	PMID:12873855	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002650	PMID:12873855	PCS		2/18			P	HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003487	PMID:12873855	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001761	PMID:12873855	PCS		8/18			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002497	OMIM:270550	TAS					P	HPO:probinson[2012-04-25]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0000012	PMID:12873855	PCS		12/18			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001260	PMID:12873855	PCS		14/18			P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003383	PMID:12873855	PCS					P	HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002493	OMIM:270550	IEA					P	HPO:iea[2009-02-17]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0007772	OMIM:270550	IEA					P	HPO:skoehler[2010-06-18]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0000007	PMID:12873855	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0002527	OMIM:270550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0003438	PMID:12873855	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:270550	Spastic ataxia, Charlevoix-Saguenay type		HP:0001257	PMID:12873855	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-02-02]
OMIM:612644	Deafness, autosomal dominant 2B		HP:0005101	OMIM:612644	TAS					P	HPO:probinson[2013-04-06]
OMIM:612644	Deafness, autosomal dominant 2B		HP:0000006	OMIM:612644	TAS					I	HPO:probinson[2013-01-09]
OMIM:207900	Argininosuccinic aciduria		HP:0001254	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0003355	OMIM:207900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:207900	Argininosuccinic aciduria		HP:0001250	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0001395	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0001251	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0002240	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0002181	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0034734	PMID:7682674	PCS		3/3			P	HPO:probinson[2023-06-05]
OMIM:207900	Argininosuccinic aciduria		HP:0011359	OMIM:207900	TAS					P	HPO:skoehler[2013-06-03]
OMIM:207900	Argininosuccinic aciduria		HP:0001508	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0000737	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0001987	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0008872	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0009886	OMIM:207900	IEA					P	HPO:skoehler[2010-06-18]
OMIM:207900	Argininosuccinic aciduria		HP:0001249	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0002038	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0003623	OMIM:207900	TAS					C	HPO:probinson[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0031956	OMIM:207900	IEA					P	HPO:skoehler[2019-02-22]
OMIM:207900	Argininosuccinic aciduria		HP:0002013	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0005961	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0002299	OMIM:207900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:207900	Argininosuccinic aciduria		HP:0001263	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0032491	PMID:21290785	PCS					P	HPO:probinson[2024-02-27]
OMIM:207900	Argininosuccinic aciduria		HP:0000007	OMIM:207900	IEA					I	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0001951	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0003217	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0001950	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
OMIM:207900	Argininosuccinic aciduria		HP:0003218	OMIM:207900	TAS					P	HPO:skoehler[2013-06-05]
OMIM:207900	Argininosuccinic aciduria		HP:0001259	OMIM:207900	IEA					P	HPO:iea[2009-02-17]
DECIPHER:57	17q21.31 recurrent microdeletion syndrome		HP:0000276	DECIPHER:57	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:57	17q21.31 recurrent microdeletion syndrome		HP:0001518	DECIPHER:57	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:57	17q21.31 recurrent microdeletion syndrome		HP:0001252	DECIPHER:57	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:57	17q21.31 recurrent microdeletion syndrome		HP:0008872	DECIPHER:57	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:57	17q21.31 recurrent microdeletion syndrome		HP:0001249	DECIPHER:57	IEA					P	HPO:skoehler[2013-05-29]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001396	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003236	OMIM:615895	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002840	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003676	PMID:23104095	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001250	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001395	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003075	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002240	PMID:23104095	PCS		2/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003593	PMID:23104095	PCS		1/3			C	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0032435	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001508	PMID:23104095	PCS		3/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001903	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002718	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002716	PMID:23104095	PCS		2/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001324	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003701	OMIM:615895	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002910	OMIM:615895	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001942	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001744	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001644	PMID:23104095	PCS		1/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003326	OMIM:615895	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003623	PMID:23104095	PCS		2/3			C	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0003202	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002037	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0000076	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002573	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002650	OMIM:615895	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0000508	OMIM:615895	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0000007	PMID:23104095	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001635	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0000964	OMIM:615895	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001019	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001954	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001638	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0008404	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001510	OMIM:615895	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002027	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0000963	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002028	PMID:23104095	PCS		2/3			P	HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0002721	PMID:23104095	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2022-08-15]
OMIM:615895	Polyglucosan body myopathy 1 with or without immunodeficiency		HP:0001974	PMID:23104095	PCS		1/3			P	HPO:probinson[2022-08-15]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0000640	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0001272	PMID:30084953	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0002120	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0002066	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0002141	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0000716	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0000718	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0025710	PMID:30084953	PCS		2/2			C	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0006895	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0002359	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0001268	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0001348	PMID:30084953	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0001347	PMID:30084953	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0000473	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0002015	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0001288	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0002497	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0001260	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0002171	PMID:30084953	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0008003	PMID:30084953	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0000007	PMID:30084953	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0000741	PMID:30084953	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0001257	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0007338	PMID:30084953	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:618369	Spinocerebellar ataxia, autosomal recessive 27		HP:0003677	PMID:30084953	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:615665	Joubert syndrome 22		HP:0000550	PMID:24166846	PCS		1/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0003577	PMID:30423442	IEA		1/1			C	HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0000089	PMID:24166846	PCS		1/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0002079	PMID:30423442	PCS		1/1			P	HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0001162	OMIM:615665;PMID:30423442	PCS		11/11			P	HPO:probinson[2021-01-02];HPO:skoehler[2014-04-13]
OMIM:615665	Joubert syndrome 22		HP:0001263	OMIM:615665	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615665	Joubert syndrome 22		HP:0004691	PMID:24166846	PCS		1/3			P	HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0001290	PMID:30423442	PCS		1/1			P	HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0001999	PMID:24166846	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0000657	PMID:30423442	PCS		1/1			P	HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0007112	PMID:30423442	PCS		1/1			P	HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0000568	PMID:24166846	PCS		2/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0000007	PMID:24166846	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0002419	PMID:24166846;PMID:30423442	PCS		11/11			P	HPO:probinson[2021-01-02];HPO:skoehler[2014-06-24];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0007973	PMID:24166846	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0001511	PMID:24166846	PCS	HP:0030674				P	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0001830	PMID:24166846;PMID:30423442	PCS		11/11			P	HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0000589	PMID:24166846	PCS		1/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2021-01-02]
OMIM:615665	Joubert syndrome 22		HP:0002335	PMID:30423442	PCS		1/1			P	HPO:probinson[2021-01-02]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0002069	PMID:38579670	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0002266	PMID:38579670	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0002197	PMID:38579670	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0002121	PMID:38579670	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0001252	PMID:38579670	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0003593	PMID:38579670	PCS		7/8			C	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0032794	PMID:38579670	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0012736	PMID:38579670	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0033725	PMID:38579670	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0012469	PMID:38579670	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0012520	PMID:38579670	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0011166	PMID:38579670	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0011463	PMID:38579670	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0032792	PMID:38579670	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0500147	PMID:38579670	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0200134	PMID:38579670	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0003429	PMID:38579670	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0011170	PMID:38579670	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0007359	PMID:38579670	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0500198	PMID:38579670	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:620806	Developmental and epileptic encephalopathy 116		HP:0000006	PMID:38579670	PCS					I	ORCID:0000-0002-0736-9199[2024-07-07]
OMIM:618341	Spermatogenic failure 35		HP:0032560	PMID:30683861	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-15]
OMIM:618341	Spermatogenic failure 35		HP:0003251	PMID:30683861	PCS		2/2			P	HPO:probinson[2022-12-15]
OMIM:618341	Spermatogenic failure 35		HP:0011462	PMID:30683861	PCS		2/2			C	HPO:probinson[2022-12-15]
OMIM:618341	Spermatogenic failure 35		HP:0000007	PMID:30683861	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-15]
OMIM:618341	Spermatogenic failure 35		HP:0033525	PMID:30683861	PCS		1/2			P	HPO:probinson[2022-12-15]
OMIM:618341	Spermatogenic failure 35		HP:0032558	PMID:30683861	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-15]
OMIM:618341	Spermatogenic failure 35		HP:0032559	PMID:30683861	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-15]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003687	PMID:24856141	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003236	PMID:24856141	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003621	PMID:24856141	PCS		1/2			C	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0100490	PMID:24856141	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003551	PMID:24856141	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0002460	PMID:24856141	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003560	PMID:24856141	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0032359	PMID:24856141	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0100297	PMID:24856141	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0007181	PMID:24856141	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0034392	PMID:24856141	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0025708	PMID:24856141	PCS		1/2			C	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0006682	PMID:24856141	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0000007	PMID:24856141	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0009697	PMID:24856141	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0006466	PMID:24856141	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0001324	PMID:24856141	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003306	PMID:24856141	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003677	PMID:24856141	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:617072	Muscular dystrophy, limb-girdle, type 2Y		HP:0003557	PMID:24856141	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:600268	Oculoectodermal syndrome		HP:0000286	OMIM:600268	IEA					P	HPO:skoehler[2010-06-18]
OMIM:600268	Oculoectodermal syndrome		HP:0000242	OMIM:600268	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600268	Oculoectodermal syndrome		HP:0000483	OMIM:600268	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600268	Oculoectodermal syndrome		HP:0007759	OMIM:600268	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600268	Oculoectodermal syndrome		HP:0000384	PMID:25808193	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0003577	PMID:25808193	PCS		2/2			C	HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0000486	OMIM:600268	IEA					P	HPO:iea[2009-02-17]
OMIM:600268	Oculoectodermal syndrome		HP:0001057	PMID:25808193	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0001250	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0000482	OMIM:600268	IEA					P	HPO:skoehler[2019-09-07]
OMIM:600268	Oculoectodermal syndrome		HP:0012803	OMIM:600268	TAS					P	HPO:skoehler[2014-06-24]
OMIM:600268	Oculoectodermal syndrome		HP:0000639	OMIM:600268	IEA					P	HPO:skoehler[2019-09-07]
OMIM:600268	Oculoectodermal syndrome		HP:0100702	OMIM:600268	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600268	Oculoectodermal syndrome		HP:0002836	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0000953	OMIM:600268	IEA					P	HPO:iea[2009-02-17]
OMIM:600268	Oculoectodermal syndrome		HP:0000752	OMIM:600268	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:600268	Oculoectodermal syndrome		HP:0001643	OMIM:600268	IEA					P	HPO:skoehler[2019-09-07]
OMIM:600268	Oculoectodermal syndrome		HP:0001004	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0000256	PMID:25808193	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0002558	OMIM:600268	IEA					P	HPO:skoehler[2019-09-07]
OMIM:600268	Oculoectodermal syndrome		HP:0000533	PMID:25808193	PCS		1/2			P	HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0010816	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0000431	OMIM:600268	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600268	Oculoectodermal syndrome		HP:0001442	OMIM:600268	IEA					I	HPO:skoehler[2019-09-07]
OMIM:600268	Oculoectodermal syndrome		HP:0001140	OMIM:600268;PMID:25808193	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0001263	PMID:25808193	PCS		0/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0001680	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0000470	OMIM:600268	IEA					P	HPO:skoehler[2019-09-07]
OMIM:600268	Oculoectodermal syndrome		HP:0005280	OMIM:600268	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600268	Oculoectodermal syndrome		HP:0012683	PMID:25808193	PCS		1/2			P	HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0001639	OMIM:600268	IEA					P	HPO:skoehler[2019-09-07]
OMIM:600268	Oculoectodermal syndrome		HP:0007572	PMID:25808193	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0100559	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0100955	PMID:25808193	PCS		1/2			P	HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0000625	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0002326	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0001631	PMID:25808193	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0001510	PMID:25808193	PCS		1/2			P	HPO:skoehler[2013-06-04];HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0000520	OMIM:600268	TAS					P	HPO:skoehler[2013-06-04]
OMIM:600268	Oculoectodermal syndrome		HP:0000006	PMID:25808193	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-28]
OMIM:600268	Oculoectodermal syndrome		HP:0000324	OMIM:600268	IEA					P	HPO:skoehler[2019-09-07]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000044	OMIM:275400	IEA					P	HPO:iea[2009-02-17]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0003477	PMID:30097146;PMID:25480986	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0003510	OMIM:275400	TAS					P	HPO:skoehler[2015-01-21]
OMIM:275400	Oliver-McFarlane syndrome		HP:0010627	PMID:25480986	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0001596	PMID:25480986	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0004322	PMID:30097146;PMID:25480986	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0003693	OMIM:275400	TAS					P	HPO:probinson[2012-07-25]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0007818	OMIM:275400	IEA					P	HPO:iea[2009-02-17]
OMIM:275400	Oliver-McFarlane syndrome		HP:0002066	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0001251	PMID:25480986	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0002460	OMIM:275400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000580	PMID:16152639	PCS		2/2			P	HPO:probinson[2017-12-22];HPO:probinson[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0010442	PMID:30097146;PMID:25480986	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0002080	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0008070	PMID:16152639;PMID:30097146	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-19];HP:probinson[2019-03-01]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000639	PMID:30097146;OMIM:275400	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17]
OMIM:275400	Oliver-McFarlane syndrome		HP:0011462	PMID:30097146	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0002317	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0000135	PMID:30097146;PMID:25480986	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0008736	OMIM:275400	IEA					P	HPO:iea[2009-02-17]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0001249	PMID:30097146;PMID:25480986	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17]
OMIM:275400	Oliver-McFarlane syndrome		HP:0006855	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0000533	PMID:30097146;PMID:25480986	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0001265	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0000054	PMID:25480986	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0002750	PMID:25480986	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0001761	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0001260	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0034323	PMID:30097146;PMID:25480986	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-McFarlane syndrome		HP:0011003	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0001518	OMIM:275400	IEA					P	HPO:iea[2009-02-17]
OMIM:275400	Oliver-McFarlane syndrome		HP:0008202	PMID:30097146	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000007	PMID:25480986	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:275400	Oliver-McFarlane syndrome		HP:0000821	PMID:30097146;PMID:25480986	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000546	PMID:30097146	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000824	PMID:25480986	PCS		6/6			P	HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000527	PMID:16152639;PMID:30097146;PMID:25480986	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17];HP:probinson[2019-03-01]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000823	OMIM:275400	IEA					P	HPO:iea[2009-02-17]
OMIM:275400	Oliver-McFarlane syndrome		HP:0001258	PMID:25480986	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:275400	Oliver-Mcfarlane syndrome		HP:0000028	OMIM:275400	IEA					P	HPO:iea[2009-02-17]
OMIM:275400	Oliver-McFarlane syndrome		HP:0001513	PMID:25480986	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0003445	OMIM:608634	IEA					P	HPO:iea[2009-02-17]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0001288	OMIM:608634	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0009053	OMIM:608634	TAS					P	HPO:probinson[2009-02-17]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0003581	OMIM:608634	IEA					C	HPO:iea[2009-02-17]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0009830	OMIM:608634	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0003470	OMIM:608634	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0002601	OMIM:608634	IEA					P	HPO:iea[2009-02-17]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0000006	PMID:15122254	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0002522	OMIM:608634	IEA					P	HPO:iea[2009-02-17]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0003677	OMIM:608634	IEA					C	HPO:skoehler[2010-06-19]
OMIM:608634	Neuronopathy, distal hereditary motor, type IIB		HP:0002600	OMIM:608634	IEA					P	HPO:iea[2009-02-17]
OMIM:267010	Meckel syndrome, type 7		HP:0003774	PMID:18371931	PCS	HP:0003593	2/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001650	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001562	PMID:18371931	PCS	HP:0030674	3/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001276	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001396	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001696	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0000023	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0002190	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0100611	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001409	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001408	PMID:15666242	PCS					P	HPO:skoehler[2015-04-26]
OMIM:267010	Meckel syndrome, type 7		HP:0000239	PMID:18371931	PCS		1/5			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0000007	PMID:18371931	PCS					I	HPO:skoehler[2015-12-30]
OMIM:267010	Meckel syndrome, type 7		HP:0001305	PMID:18371931	PCS		1/5			P	HPO:skoehler[2015-12-30]
OMIM:267010	Meckel syndrome, type 7		HP:0000348	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001737	PMID:18371931	PCS		2/12			P	HPO:probinson[2018-03-05];HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001643	PMID:18371931	PCS	HP:0030674	2/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001830	PMID:18371931	PCS	HP:0003577	1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0000003	PMID:18371931	PCS		6/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001631	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0002613	PMID:18371931	PCS		2/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001433	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:267010	Meckel syndrome, type 7		HP:0001667	PMID:18371931	PCS		1/7			P	HPO:probinson[2018-03-31]
OMIM:614209	Meckel syndrome, type 9		HP:0009826	PMID:21493627	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0001762	PMID:21493627	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0000062	PMID:21493627	PCS		1/1			P	HPO:skoehler[2015-04-26];HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0034199	PMID:21493627	PCS		1/1			C	HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0002085	PMID:21493627	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0000932	PMID:21493627	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0000007	PMID:21493627	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0000003	PMID:21493627	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614209	Meckel syndrome, type 9		HP:0034217	PMID:21493627	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:190420	Triglyceride storage disease, type I		HP:0004325	OMIM:190420	TAS					P	HPO:probinson[2009-02-17]
OMIM:190420	Triglyceride storage disease, type I		HP:0000252	OMIM:190420	TAS					P	HPO:probinson[2009-02-17]
OMIM:618433	Spermatogenic failure 38		HP:0032560	PMID:30686508	PCS		4/5			P	HPO:probinson[2019-09-15]
OMIM:618433	Spermatogenic failure 38		HP:0003251	PMID:30686508	TAS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618433	Spermatogenic failure 38		HP:0032562	PMID:30686508	PCS		4/4			P	HPO:probinson[2019-09-15]
OMIM:618433	Spermatogenic failure 38		HP:0012207	PMID:30686508	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-15]
OMIM:618433	Spermatogenic failure 38		HP:0000007	PMID:30686508	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-15]
OMIM:618433	Spermatogenic failure 38		HP:0012258	PMID:30686508	TAS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618433	Spermatogenic failure 38		HP:0000798	PMID:30686508	TAS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618433	Spermatogenic failure 38		HP:0032558	PMID:30686508	PCS					P	HPO:probinson[2019-09-15]
OMIM:618433	Spermatogenic failure 38		HP:0012865	PMID:30686508	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:146700	Ichthyosis vulgaris		HP:0008064	PMID:16444271	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-11-26]
OMIM:146700	Ichthyosis vulgaris		HP:0000958	PMID:23301728	PCS					P	HPO:probinson[2020-11-26]
OMIM:146700	Ichthyosis vulgaris		HP:0032152	PMID:23301728	PCS					P	HPO:probinson[2020-11-26]
OMIM:146700	Ichthyosis vulgaris		HP:0002099	PMID:23301728	PCS		HP:0040282			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-26]
OMIM:146700	Ichthyosis vulgaris		HP:0011463	PMID:23301728	PCS					C	HPO:probinson[2020-11-26]
OMIM:146700	Ichthyosis vulgaris		HP:0033252	PMID:23301728	PCS					P	HPO:probinson[2020-12-07]
OMIM:146700	Ichthyosis vulgaris		HP:0033807	PMID:16444271	PCS		1/1			P	HPO:probinson[2021-06-13]
OMIM:146700	Ichthyosis vulgaris		HP:0000964	PMID:23301728	PCS		HP:0040282			P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-26]
OMIM:146700	Ichthyosis vulgaris		HP:0000007	PMID:16444271	PCS					I	HPO:probinson[2020-11-26]
OMIM:146700	Ichthyosis vulgaris		HP:0000006	PMID:16444271	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-26]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002322	PMID:26026163	PCS		1/16			P	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0001498	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0004322	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002066	PMID:26026163	PCS		4/15			P	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0000020	PMID:26026163	PCS		2/16			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002020	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002064	PMID:26026163	PCS		14/15			P	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002460	PMID:26026163	PCS		15/16			P	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002061	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0000518	PMID:26026163	PCS		2/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0000639	PMID:26026163	PCS		2/16			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0011462	PMID:26026163	PCS					C	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0001328	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0003700	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0001347	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002036	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0003621	PMID:26026163	PCS					C	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0003487	PMID:26026163	PCS		12/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002750	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0001288	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0001761	PMID:26026163	PCS		7/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0000012	PMID:26026163	PCS		4/16			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002013	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002395	PMID:26026163	PCS		16/16			P	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0001260	PMID:26026163	PCS		5/15			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002495	PMID:26026163	PCS		3/16			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0031993	PMID:26026163	PCS		8/9			P	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0007371	PMID:26026163	PCS		1/16			P	HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0007299	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0007178	PMID:26026163	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0001258	PMID:26026163	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0000006	PMID:26026163	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0003677	PMID:26026163	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002644	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:601162	Spastic paraplegia 9A, autosomal dominant		HP:0002127	OMIM:601162	IEA					P	HPO:iea[2009-02-17]
OMIM:609258	Myopia 9		HP:0000545	OMIM:609258	TAS					P	HPO:skoehler[2014-10-17]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0003577	PMID:27008887	PCS		3/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0002540	PMID:27008887	PCS		4/4			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0001252	PMID:27008887	PCS		4/4		HP:0012828	P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0001270	PMID:27008887	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0100297	PMID:27008887	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0000958	PMID:27008887	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0034045	PMID:27008887	PCS		1/3			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0032341	PMID:27008887	PCS		2/2			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0000218	PMID:27008887	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0003327	PMID:27008887	PCS		4/4			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0007502	PMID:27008887	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0003306	PMID:27008887	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0003623	PMID:27008887	PCS		1/4			C	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0003687	PMID:27008887	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0002650	PMID:27008887	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0011968	PMID:27008887	PCS		3/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0001382	PMID:27008887	PCS		4/4			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0003560	PMID:27008887	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0008081	PMID:27008887	PCS		2/3			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0034392	PMID:27008887	PCS		2/4			P	HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0000767	PMID:27008887	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0000007	PMID:27008887	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0002747	PMID:27008887	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0000467	PMID:27008887	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-18]
OMIM:617066	Muscular dystrophy, congenital, Davignon-Chauveau type		HP:0003557	PMID:27008887	PCS		3/3			P	HPO:probinson[2023-04-18]
OMIM:605462	Basal cell carcinoma, susceptibility to, 1		HP:0002671	OMIM:605462	IEA					P	HPO:skoehler[2013-01-09]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0001397	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0001252	OMIM:231530	TAS					P	HPO:probinson[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0002173	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0006929	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0001290	OMIM:231530	TAS					P	HPO:skoehler[2017-07-13]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0100950	OMIM:231530	IEA					P	HPO:skoehler[2018-10-08]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0001639	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0002605	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0002913	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0000007	OMIM:231530	TAS					I	HPO:probinson[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0008872	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0001510	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0003215	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0004448	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0001644	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:231530	3-Hydroxyacyl-Coa dehydrogenase deficiency		HP:0001985	OMIM:231530	IEA					P	HPO:iea[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0003510	OMIM:256540	IEA					P	HPO:iea[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0007759	OMIM:256540	IEA					P	HPO:iea[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0000365	OMIM:256540	IEA					P	HPO:iea[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0001250	OMIM:256540	IEA					P	HPO:iea[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0001790	PMID:19466716	PCS	HP:0030674				P	HP:probinson[2018-09-17]
OMIM:256540	Galactosialidosis		HP:0010729	PMID:23915561	PCS	HP:0003593				P	HPO:skoehler[2009-02-17];HP:probinson[2018-09-17]
OMIM:256540	Galactosialidosis		HP:0003271	PMID:23915561	PCS	HP:0003593				P	HP:probinson[2018-09-17]
OMIM:256540	Galactosialidosis		HP:0000280	PMID:23915561	PCS	HP:0003593				P	HPO:iea[2009-02-17];HP:probinson[2018-09-17]
OMIM:256540	Galactosialidosis		HP:0008166	OMIM:256540	TAS					P	HPO:probinson[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0000943	OMIM:256540	IEA					P	HPO:iea[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0000524	OMIM:256540	IEA					P	HPO:iea[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0000007	PMID:8725271	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:256540	Galactosialidosis		HP:0001433	OMIM:256540	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:256540	Galactosialidosis		HP:0001249	PMID:23915561	PCS		4/4			P	HPO:iea[2009-02-17];HP:probinson[2018-09-17]
OMIM:256540	Galactosialidosis		HP:0001028	OMIM:256540	IEA					P	HPO:skoehler[2010-06-20]
OMIM:615842	Spermatogenic failure 14		HP:0030345	PMID:24431330	PCS		0/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0031040	PMID:24431330	PCS		3/3			P	HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0003251	PMID:24431330	PCS		3/3			P	HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0011462	PMID:24431330	PCS		3/3			C	HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0008232	PMID:24431330	PCS		3/3			P	HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0030087	PMID:24431330	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0000007	PMID:24431330	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0040086	PMID:24431330	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-12-12]
OMIM:615842	Spermatogenic failure 14		HP:0000027	PMID:24431330	PCS		3/3			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-12-12]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000286	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0010804	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0003577	PMID:24697219	PCS		2/2			C	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0001251	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0011412	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0012469	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000718	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000733	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000218	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0002714	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0003763	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000252	PMID:24697219	PCS		2/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0008935	PMID:24697219	PCS		2/2			P	HPO:probinson[2022-06-19];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000494	PMID:24697219	PCS		1/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0002059	PMID:24697219	PCS		2/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0001762	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0001344	PMID:24697219	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000232	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000293	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000490	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0001263	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0010818	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0005280	PMID:24697219	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0012167	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0100716	PMID:24697219	PCS		1/2			P	HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000369	PMID:24697219	PCS		1/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-06-19]
OMIM:616393	Intellectual developmental disorder, autosomal dominant 38		HP:0000006	PMID:24697219	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-19]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0000341	PMID:27066583	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0002059	PMID:27066583	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0002266	PMID:27066583	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0001250	PMID:27066583	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0000194	PMID:27066583	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0005484	PMID:27066583	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0003593	PMID:27066583	PCS		1/1			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0001290	PMID:27066583	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0012471	PMID:27066583	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0000817	PMID:27066583	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0000007	PMID:27066583	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0000648	PMID:27066583	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0200134	PMID:27066583	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0007334	PMID:27066583	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0002505	PMID:27066583	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0000218	PMID:27066583	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0001257	OMIM:617933	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617933	Epileptic encephalopathy, early infantile, 61		HP:0002104	PMID:27066583	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001773	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001156	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001552	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0004322	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000581	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0011611	OMIM:300712	TAS			MALE		P	HPO:skoehler[2012-11-21]
OMIM:300712	Craniofacioskeletal syndrome		HP:0012745	OMIM:300712	TAS			MALE		P	HPO:skoehler[2014-03-24]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001629	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000914	OMIM:300712	TAS			MALE		P	HPO:skoehler[2014-06-24]
OMIM:300712	Craniofacioskeletal syndrome		HP:0008551	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000239	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0002738	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000219	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000219	OMIM:300712	TAS			FEMALE		P	HPO:skoehler[2013-06-04]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001643	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0002777	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0006610	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001423	OMIM:300712	TAS					I	HPO:skoehler[2013-05-29]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001763	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000358	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000175	OMIM:300712	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000252	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000494	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000453	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000453	OMIM:300712	TAS			MALE		P	HPO:skoehler[2012-11-21]
OMIM:300712	Craniofacioskeletal syndrome		HP:0004279	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001321	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001263	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0011467	OMIM:300712	TAS			MALE		P	HPO:skoehler[2012-11-21]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001419	OMIM:300712	TAS					I	HPO:skoehler[2012-11-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0002868	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0002901	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0004209	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001511	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0200055	OMIM:300712	TAS					P	HPO:skoehler[2012-11-21]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000047	OMIM:300712	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000322	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0001631	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000028	OMIM:300712	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000325	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000347	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000126	OMIM:300712	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300712	Craniofacioskeletal syndrome		HP:0000126	OMIM:300712	TAS			MALE		P	HPO:skoehler[2012-11-21]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0001265	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0002751	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0002345	OMIM:180800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003621	OMIM:180800	IEA					C	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003431	OMIM:180800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0001761	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003693	OMIM:180800	TAS					P	HPO:probinson[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0002066	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003383	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0001284	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0002460	OMIM:180800	TAS					P	HPO:probinson[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003382	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003481	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0001270	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003380	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0007351	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0002715	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0002936	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0000006	OMIM:180800	IEA					I	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0003677	OMIM:180800	IEA					C	HPO:iea[2009-02-17]
OMIM:180800	Roussy-Levy hereditary areflexic dystasia		HP:0001765	OMIM:180800	IEA					P	HPO:iea[2009-02-17]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0012132	OMIM:237800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0002904	OMIM:237800	IEA					P	HPO:iea[2009-02-17]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0002240	OMIM:237800	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0000007	OMIM:237800	IEA					I	HPO:iea[2009-02-17]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0010972	OMIM:237800	TAS					P	HPO:skoehler[2012-11-20]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0001923	OMIM:237800	TAS					P	HPO:skoehler[2012-11-20]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0000952	OMIM:237800	IEA					P	HPO:iea[2009-02-17]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0001744	OMIM:237800	IEA					P	HPO:iea[2009-02-17]
OMIM:237800	Hyperbilirubinemia, shunt, primary		HP:0000006	OMIM:237800	TAS					I	HPO:skoehler[2012-11-20]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000891	OMIM:617927	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000582	OMIM:617927	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000321	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000431	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0001156	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0004322	OMIM:617927	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0002750	OMIM:617927	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000020	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000350	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0410030	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000191	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0100259	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0100258	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0009882	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0005819	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000426	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000954	OMIM:617927	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000007	PMID:27060890	PCS					I	HP:probinson[2019-02-19]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0002857	OMIM:617927	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0001852	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000322	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617927	Orofaciodigital syndrome XVIII		HP:0000699	OMIM:617927	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003202	OMIM:608807	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003236	PMID:25772186;OMIM:608807	PCS		11/11		HP:0012825	P	HPO:probinson[2009-02-17];HPO:skoehler[2010-06-20];HPO:probinson[2022-12-13]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003676	OMIM:608807	IEA					C	HPO:skoehler[2019-09-07]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003551	PMID:25772186	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0002460	OMIM:608807	IEA					P	HPO:iea[2009-02-17]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003560	OMIM:608807	IEA					P	HPO:iea[2009-02-17]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0012548	PMID:25772186	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0025708	PMID:25772186	PCS		1/1			C	HPO:probinson[2022-12-13]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0011463	OMIM:608807	TAS					C	HPO:probinson[2012-07-24]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0000007	PMID:12145747	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0001638	PMID:25772186	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-13]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003701	PMID:25772186	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003458	OMIM:608807	IEA					P	HPO:iea[2009-02-17]
OMIM:608807	Muscular dystrophy, limb-girdle, autosomal recessive 10		HP:0003557	PMID:25772186	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:620153	Mosaic variegated aneuploidy syndrome 4		HP:0000252	PMID:34009673	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:620153	Mosaic variegated aneuploidy syndrome 4		HP:0003220	PMID:34009673	PCS					P	HPO:probinson[2023-03-04]
OMIM:620153	Mosaic variegated aneuploidy syndrome 4		HP:0011342	PMID:34009673	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:620153	Mosaic variegated aneuploidy syndrome 4		HP:0000007	PMID:34009673	PCS					I	HPO:probinson[2023-03-04]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0000253	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001298	OMIM:610090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0003785	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0008936	OMIM:610090	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001276	OMIM:610090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001583	PMID:12200739	PCS					P	HPO:lccarmody[2018-10-18]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001250	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0002151	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001263	OMIM:610090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001508	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001903	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0000007	OMIM:610090	IEA					I	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001943	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0008872	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0002317	OMIM:610090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001942	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001336	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:610090	Pyridoxamine 5-prime-phosphate oxidase deficiency		HP:0001622	OMIM:610090	IEA					P	HPO:iea[2009-02-17]
OMIM:620635	Cardiomyopathy, dilated, 2J		HP:0001684	PMID:37561591	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620635	Cardiomyopathy, dilated, 2J		HP:0003593	PMID:32870709;PMID:37561591	PCS		3/3			C	HPO:probinson[2024-03-12]
OMIM:620635	Cardiomyopathy, dilated, 2J		HP:0000007	PMID:32870709	PCS					I	HPO:probinson[2024-03-12]
OMIM:620635	Cardiomyopathy, dilated, 2J		HP:0001635	PMID:37561591	PCS		2/3			P	HPO:probinson[2024-03-12]
OMIM:620635	Cardiomyopathy, dilated, 2J		HP:0012666	PMID:37561591	PCS		3/3			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620635	Cardiomyopathy, dilated, 2J		HP:0001644	PMID:37561591	PCS		3/3			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0002014	PMID:27523608	PCS	HP:0003623	3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0001386	PMID:27523608	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0001531	PMID:27559085	PCS		3/3			P	HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0003496	PMID:27523608	PCS		3/3			P	HPO:probinson[2020-10-28]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0003593	PMID:27559085	PCS		3/3			C	HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0003261	PMID:27523608	PCS		3/3			P	HPO:probinson[2020-10-28]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0011897	PMID:27523608	PCS	HP:0003623	3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0011227	PMID:27523608	PCS	HP:0003623	3/3			P	HPO:probinson[2020-10-28]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0002829	PMID:27559085	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0000007	PMID:27523608	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0009125	PMID:27559085	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0002716	PMID:27559085	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0001954	PMID:27559085	PCS		3/3			P	HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0012490	PMID:27559085;PMID:27523608	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-28];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0000988	PMID:27559085	PCS		3/3			P	HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0002027	PMID:27559085	PCS		1/3			P	HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0001974	PMID:27523608	PCS	HP:0003623	3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-28]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0003326	PMID:27559085	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0002633	PMID:27559085	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617099	Autoinflammation, panniculitis, and dermatosis syndrome		HP:0002028	PMID:27559085	PCS		1/3			P	HPO:probinson[2020-11-26]
OMIM:145590	Hyperthermia, cutaneous, with headaches and nausea		HP:0002013	OMIM:145590	IEA					P	HPO:iea[2009-02-17]
OMIM:145590	Hyperthermia, cutaneous, with headaches and nausea		HP:0001945	OMIM:145590	TAS					P	HPO:probinson[2009-02-17]
OMIM:145590	Hyperthermia, cutaneous, with headaches and nausea		HP:0002018	OMIM:145590	IEA					P	HPO:iea[2009-02-17]
OMIM:145590	Hyperthermia, cutaneous, with headaches and nausea		HP:0002315	OMIM:145590	TAS					P	HPO:probinson[2009-02-17]
OMIM:145590	Hyperthermia, cutaneous, with headaches and nausea		HP:0000006	OMIM:145590	IEA					I	HPO:iea[2009-02-17]
OMIM:209050	Athrombia, essential		HP:0001892	OMIM:209050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:209050	Athrombia, essential		HP:0008352	OMIM:209050	IEA					P	HPO:iea[2009-02-17]
OMIM:209050	Athrombia, essential		HP:0003540	OMIM:209050	TAS					P	HPO:probinson[2012-05-30]
OMIM:209050	Athrombia, essential		HP:0003010	OMIM:209050	TAS					P	HPO:probinson[2009-02-17]
OMIM:209050	Athrombia, essential		HP:0000007	OMIM:209050	IEA					I	HPO:iea[2009-02-17]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0000494	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0001264	OMIM:300048	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0004389	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0002013	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0002021	OMIM:300048	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0001250	OMIM:300048	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0003593	OMIM:300048	PCS					C	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0011877	OMIM:300048	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0003270	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0030889	OMIM:300048	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0000319	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0001419	OMIM:300048	PCS					I	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0000316	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0001999	OMIM:300048	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0040309	OMIM:300048	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0008872	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0001643	OMIM:300048	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0001873	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0000369	OMIM:300048	PCS					P	HPO:probinson[2012-03-26]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0002566	OMIM:300048	TAS					P	HPO:skoehler[2013-05-29]
OMIM:300048	Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked		HP:0000126	OMIM:300048	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:241000	Hypogonadism with low-grade mental deficiency and microcephaly		HP:0000252	OMIM:241000	TAS					P	HPO:probinson[2009-02-17]
OMIM:241000	Hypogonadism with low-grade mental deficiency and microcephaly		HP:0010714	OMIM:241000	TAS					P	HPO:probinson[2009-02-17]
OMIM:241000	Hypogonadism with low-grade mental deficiency and microcephaly		HP:0000007	OMIM:241000	TAS					I	HPO:probinson[2009-02-17]
OMIM:241000	Hypogonadism with low-grade mental deficiency and microcephaly		HP:0000026	OMIM:241000	TAS					P	HPO:probinson[2009-02-17]
OMIM:241000	Hypogonadism with low-grade mental deficiency and microcephaly		HP:0001159	OMIM:241000	TAS					P	HPO:probinson[2009-02-17]
OMIM:241000	Hypogonadism with low-grade mental deficiency and microcephaly		HP:0001249	OMIM:241000	TAS					P	HPO:skoehler[2010-06-18]
OMIM:241000	Hypogonadism with low-grade mental deficiency and microcephaly		HP:0000027	OMIM:241000	TAS					P	HPO:probinson[2012-07-18]
OMIM:260970	Peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and		HP:0001271	OMIM:260970	IEA					P	HPO:iea[2009-02-17]
OMIM:260970	Peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and		HP:0001251	OMIM:260970	IEA					P	HPO:iea[2009-02-17]
OMIM:260970	Peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and		HP:0000007	OMIM:260970	IEA					I	HPO:iea[2009-02-17]
OMIM:260970	Peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and		HP:0007267	OMIM:260970	TAS					P	HPO:iea[2015-04-18]
OMIM:260970	Peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and		HP:0007313	OMIM:260970	TAS					P	HPO:iea[2015-04-18]
OMIM:260970	Peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and		HP:0006976	OMIM:260970	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0008605	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000486	PMID:34344887	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000086	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0011342	PMID:34344887	PCS		3/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0002937	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000238	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0002857	PMID:34344887	PCS		1/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000636	PMID:34344887	PCS	HP:0003577	1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0003305	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0009944	PMID:34344887	PCS	HP:0003577	1/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0001643	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0001249	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0008417	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000891	PMID:34344887	PCS		3/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000175	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0001140	PMID:34344887;OMIM:164210	PCS		11/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0100731	PMID:34344887	PCS	HP:0003577	3/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0009892	OMIM:164210	IEA					P	HPO:skoehler[2010-06-18]
OMIM:164210	Hemifacial microsomia		HP:0011332	OMIM:164210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:164210	Hemifacial microsomia		HP:0000528	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000407	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0012020	PMID:34344887	PCS		1/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000646	PMID:34344887	PCS		1/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0002308	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000327	PMID:34344887	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000568	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000405	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000003	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000006	PMID:34344887	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000204	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000324	PMID:34344887	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000384	PMID:34344887	PCS		5/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0003577	PMID:34344887	PCS		8/8			C	HPO:probinson[2022-05-15]
OMIM:164210	Hemifacial microsomia		HP:0002089	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0001274	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000581	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0004660	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0002085	OMIM:164210	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0001629	PMID:34344887	PCS	HP:0003577	1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0008551	PMID:34344887	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000413	PMID:34344887	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000154	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000076	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0002650	PMID:34344887	PCS		1/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0001680	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000272	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0000074	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0011272	PMID:34344887	PCS		1/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0011270	PMID:34344887	PCS		2/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0009794	OMIM:164210	TAS					P	HPO:probinson[2013-04-07]
OMIM:164210	Hemifacial microsomia		HP:0000508	PMID:34344887	PCS		2/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0001636	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:164210	Hemifacial microsomia		HP:0005439	PMID:34344887	PCS		2/8			P	HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000347	PMID:34344887;OMIM:164210	PCS		16/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-02]
OMIM:164210	Hemifacial microsomia		HP:0000104	OMIM:164210	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002684	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0004322	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000463	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001250	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001252	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	ASPARTYLGLUCOSAMINURIA		HP:6000573	PMID:1904874	PCS		3/3			P	HPO:probinson[2024-04-03]
OMIM:208400	Aspartylglucosaminuria		HP:0002240	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000283	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0100790	OMIM:208400	TAS					P	HPO:skoehler[2013-05-29]
OMIM:208400	Aspartylglucosaminuria		HP:0001290	OMIM:208400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:208400	Aspartylglucosaminuria		HP:0000280	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001071	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000518	OMIM:208400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208400	Aspartylglucosaminuria		HP:0011463	OMIM:208400	TAS					C	HPO:probinson[2022-04-24]
OMIM:208400	Aspartylglucosaminuria		HP:0001609	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001922	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002738	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000158	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000179	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002756	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001249	OMIM:208400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:208400	Aspartylglucosaminuria		HP:0003304	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000154	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002014	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0003302	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000252	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002059	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002650	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000750	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002376	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0002750	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001382	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000053	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001061	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0005280	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0012068	OMIM:208400	TAS					P	HPO:probinson[2012-08-04]
OMIM:208400	Aspartylglucosaminuria		HP:0002808	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0032198	OMIM:208400	IEA					P	HPO:skoehler[2019-02-22]
OMIM:208400	Aspartylglucosaminuria		HP:0001939	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000926	OMIM:208400	TAS					P	HPO:probinson[2012-06-10]
OMIM:208400	Aspartylglucosaminuria		HP:0000943	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000007	PMID:1904874	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:208400	Aspartylglucosaminuria		HP:0002205	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001257	OMIM:208400	TAS					P	HPO:skoehler[2010-06-18]
OMIM:208400	Aspartylglucosaminuria		HP:0001653	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0000248	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0001875	OMIM:208400	IEA					P	HPO:iea[2009-02-17]
OMIM:208400	Aspartylglucosaminuria		HP:0004568	OMIM:208400	TAS					P	HPO:probinson[2012-06-10]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0003581	PMID:18678517	PCS		1/1			C	HPO:probinson[2022-05-09]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0002094	PMID:18678517	PCS		1/1			P	HPO:probinson[2022-05-09]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0000007	PMID:18678517	PCS					I	HPO:probinson[2022-05-09]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0001635	PMID:18678517	PCS		1/1			P	HPO:probinson[2022-05-09]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0011713	PMID:18678517	PCS		1/1			P	HPO:probinson[2022-05-09]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0033755	PMID:18678517	PCS		1/1			P	HPO:probinson[2022-05-09]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0012666	PMID:18678517	PCS		1/1			P	HPO:probinson[2022-05-09]
OMIM:612877	Cardiomyopathy, dilated, 1BB		HP:0001644	PMID:18678517	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2022-05-09]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001332	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001250	PMID:34542157;PMID:29178645	PCS		3/3			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001272	PMID:34542157	PCS		1/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0002120	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001252	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0003593	PMID:34542157	PCS		2/2			C	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0000739	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0011461	PMID:29178645	PCS		1/1			C	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0000975	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0002119	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0005968	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0002019	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0002510	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001344	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001321	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0011968	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001263	PMID:34542157;PMID:29178645	PCS		3/3			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0002072	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0010852	PMID:34542157	PCS		1/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0033258	PMID:34542157	PCS		1/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0031358	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0034197	PMID:29178645	PCS		1/1			C	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0000007	PMID:34542157	PCS					I	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001558	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0100716	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0001511	PMID:29178645	PCS		1/1			P	HPO:probinson[2022-08-14]
OMIM:619922	Neurodevelopmental disorder with dystonia and seizures		HP:0002305	PMID:34542157	PCS		2/2			P	HPO:probinson[2022-08-14];HPO:probinson[2022-08-14]
OMIM:176600	Presenile dementia, Kraepelin type		HP:0000726	OMIM:176600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:176600	Presenile dementia, Kraepelin type		HP:0000006	OMIM:176600	IEA					I	HPO:iea[2009-02-17]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0030732	PMID:18203180	PCS		1/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001212	PMID:18203180	PCS		1/2			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001252	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0005133	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0012745	PMID:17512813;PMID:18203180	PCS		3/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0031987	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0011343	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000639	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000319	PMID:17512813;PMID:18203180	PCS		2/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0011461	PMID:9863602	PCS		1/1			C	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000238	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001643	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000176	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0030820	PMID:18203180	PCS		2/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0011968	PMID:9863602;PMID:17512813	PCS		2/2			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0011726	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001263	PMID:17512813;PMID:18203180	PCS		3/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0005180	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0002705	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001852	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000369	PMID:9863602;PMID:18203180	PCS		3/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000006	PMID:18203180	PCS					I	HPO:probinson[2022-09-04]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000324	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000341	PMID:18203180	PCS		2/2			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000582	PMID:18203180	PCS		2/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000343	PMID:17512813;PMID:18203180	PCS		2/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000463	PMID:17512813;PMID:18203180	PCS		3/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0010747	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001274	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0002162	PMID:18203180	PCS		1/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000736	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000219	PMID:17512813;PMID:18203180	PCS		3/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000218	PMID:9863602;PMID:18203180	PCS		1/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000378	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000653	PMID:18203180	PCS		1/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001545	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0025352	PMID:18203180	PCS					I	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0006956	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0002098	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0005164	PMID:18203180	PCS		1/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0034054	PMID:9863602	PCS		1/1			P	HPO:probinson[2022-02-03]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0011232	PMID:18203180	PCS		2/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0000268	PMID:9863602	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0002007	PMID:18203180	PCS		2/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001511	PMID:18203180	IEA	HP:0011461	3/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0200055	PMID:17512813	PCS		1/1			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001631	PMID:17512813;PMID:18203180	PCS		2/4			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001510	PMID:18203180	PCS		3/3			P	HPO:probinson[2021-10-22]
OMIM:612863	Chromosome 6q25-q25 deletion syndrome		HP:0001634	PMID:18203180	PCS		1/3			P	HPO:probinson[2021-10-22]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0002069	PMID:27864268	PCS		3/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0001344	PMID:27864268	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0002188	PMID:27864268	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0001266	PMID:27864268	PCS		2/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0002384	PMID:27864268	PCS		3/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0010819	PMID:27864268	PCS		2/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0001252	PMID:27864268	PCS		6/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0003593	PMID:27864268	PCS		4/8			C	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0032794	PMID:27864268	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0011147	PMID:27864268	PCS		2/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0011344	PMID:27864268	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0012469	PMID:27864268	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0007270	PMID:27864268	PCS		2/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0034295	PMID:27864268	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0000639	PMID:27864268	PCS		3/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0011463	PMID:27864268	PCS		3/8			C	HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0032792	PMID:27864268	PCS		2/8			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0200134	PMID:27864268	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0000006	PMID:27864268	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:618396	Epileptic encephalopathy, early infantile, 74		HP:0003623	PMID:27864268	PCS		1/8			C	HPO:probinson[2023-02-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0002389	PMID:37057673	PCS		2/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0003593	PMID:37057673	PCS		2/3			C	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001790	PMID:27234373;PMID:37057673	PCS		2/4			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0031964	PMID:27234373;PMID:37057673	PCS		4/4			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0012666	PMID:27234373;PMID:37057673	PCS		4/4			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0000518	PMID:27234373;PMID:37057673	PCS		2/4			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001508	PMID:27234373	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001629	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0011220	PMID:27234373	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0000316	PMID:27234373;PMID:37057673	PCS		1/4			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001987	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001943	PMID:27234373	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0002416	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001302	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0000256	PMID:27234373	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001788	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001644	PMID:37057673	PCS		3/3			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0003623	PMID:37057673	PCS		1/3			C	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0000494	PMID:27234373	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0031956	PMID:27234373;PMID:37057673	PCS		4/4			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001640	PMID:27234373	PCS	HP:0034197	1/1			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0030961	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001684	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0011968	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0002151	PMID:27234373;PMID:37057673	PCS		4/4			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0000609	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0034197	PMID:27234373	PCS		1/1			C	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0003819	PMID:27234373	PCS		1/1			C	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0001635	PMID:27234373;PMID:37057673	PCS		4/4			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0000006	PMID:27234373	PCS					I	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0000369	PMID:27234373;PMID:37057673	PCS		1/4			P	HPO:probinson[2024-03-12]
OMIM:620609	Long-Olsen-Distelmaier syndrome		HP:0002126	PMID:37057673	PCS		1/3			P	HPO:probinson[2024-03-12]
OMIM:610245	Spinocerebellar ataxia 23		HP:0002166	PMID:15306549	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0003596	PMID:21035104;PMID:15306549	PCS		4/9			C	HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0006858	PMID:15306549	PCS		3/5			P	HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0003487	PMID:15306549	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0001310	OMIM:610245	TAS					P	HPO:skoehler[2012-11-21]
OMIM:610245	Spinocerebellar ataxia 23		HP:0001272	PMID:15306549	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0001260	PMID:21035104;PMID:15306549	PCS		7/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0002066	PMID:21035104;PMID:15306549	PCS		8/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0001271	PMID:21035104	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0003584	PMID:21035104;PMID:15306549	PCS		5/9			C	HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0001274	OMIM:610245	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610245	Spinocerebellar ataxia 23		HP:0002070	PMID:21035104;PMID:15306549	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0007141	OMIM:610245	TAS					P	HPO:skoehler[2012-11-21]
OMIM:610245	Spinocerebellar ataxia 23		HP:0000514	OMIM:610245	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610245	Spinocerebellar ataxia 23		HP:0002529	OMIM:610245	TAS					P	HPO:skoehler[2012-11-21]
OMIM:610245	Spinocerebellar ataxia 23		HP:0000641	PMID:15306549	PCS		3/5			P	HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0000006	PMID:21035104	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0007305	OMIM:610245	TAS					P	HPO:skoehler[2012-11-21]
OMIM:610245	Spinocerebellar ataxia 23		HP:0003677	PMID:21035104	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0001337	PMID:21035104	PCS		3/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-16]
OMIM:610245	Spinocerebellar ataxia 23		HP:0001347	PMID:15306549	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000286	PMID:31361404	PCS		11/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0004467	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000365	PMID:31361404	PCS		3/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000463	PMID:31361404	PCS		11/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0002263	PMID:31361404	PCS		13/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0001274	PMID:31361404	PCS		3/15			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0003196	PMID:31361404	PCS		11/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0003593	PMID:31361404	PCS					C	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0001290	PMID:31361404	PCS		12/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0031348	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0001629	PMID:31361404	PCS		4/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0011342	PMID:31361404	PCS					P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0001804	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0008551	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0001647	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000954	PMID:31361404	PCS		2/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0002119	PMID:31361404	PCS		1/15			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0009623	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000411	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000378	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0002553	PMID:31361404	PCS		12/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000396	PMID:31361404	PCS		1/24		HP:0012833	P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000494	PMID:31361404	PCS		14/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000750	PMID:31361404	PCS					P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0002079	PMID:31361404	PCS		3/15			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0030048	PMID:31361404	PCS		1/15			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0011968	PMID:31361404	PCS		12/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0005487	PMID:31361404	PCS					P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000729	PMID:31361404	IEA		8/24			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000508	PMID:31361404	IEA		20/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0001712	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0009897	PMID:31361404	PCS		1/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0004209	PMID:31361404	PCS		3/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000289	PMID:31361404	PCS		13/24			P	HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000006	PMID:31361404	PCS					I	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618619	Weiss-Kruszka syndrome		HP:0000369	PMID:31361404	PCS		6/24			P	HPO:probinson[2020-07-11]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0031317	PMID:31970803	PCS		3/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0002751	PMID:31970803	PCS		2/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003577	PMID:31970803	PCS		1/4			C	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003236	PMID:31970803	PCS		4/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0002650	PMID:31970803	PCS	HP:0003577	1/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003201	PMID:31970803	PCS		4/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003551	PMID:31970803	PCS		4/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003273	PMID:31970803	PCS		4/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003593	PMID:31970803	PCS		3/4			C	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0002194	PMID:31970803	PCS		3/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0034677	PMID:31970803	PCS		3/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003391	PMID:31970803	PCS		2/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0032341	PMID:31970803	PCS		3/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0000007	PMID:31970803	PCS					I	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0001239	PMID:31970803	PCS		2/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003789	PMID:31970803	PCS		4/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003701	PMID:31970803	PCS		3/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003306	PMID:31970803	PCS		4/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0034391	PMID:31970803	PCS		4/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003325	PMID:31970803	PCS		3/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003798	PMID:31970803	PCS		2/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003557	PMID:31970803	PCS		3/4			P	HPO:probinson[2023-07-14]
OMIM:620386	Nemaline myopathy 5B, autosomal recessive, childhood-onset		HP:0003722	PMID:31970803	PCS		1/4			P	HPO:probinson[2023-07-14]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0001276	PMID:25080166	PCS					P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0000252	PMID:25080166	PCS		1/7			P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0002059	PMID:25080166	PCS		1/1			P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0001250	PMID:25080166	PCS		7/7			P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0001263	PMID:14673469	PCS		1/1			P	HPO:skoehler[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0003593	PMID:25080166	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0000007	PMID:14673469	PCS					I	HPO:skoehler[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0008897	PMID:14673469	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0001511	PMID:14673469	PCS		1/1			P	HPO:skoehler[2013-08-10];HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0012279	PMID:14673469	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:614023	Phosphoserine phosphatase deficiency		HP:0001249	PMID:25080166	PCS		7/7			P	HPO:skoehler[2015-04-19];HPO:probinson[2023-02-12]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0003676	PMID:25512002	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-19]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0003542	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0001332	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-05-19]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0001310	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0001250	PMID:25512002	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0002384	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0001260	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0002151	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0001252	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0003391	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0012378	PMID:25512002	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0031962	PMID:25512002	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0012446	PMID:25512002	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0011463	PMID:25512002	PCS		1/1			C	HPO:probinson[2023-05-19]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0000007	PMID:25512002	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0030051	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0003737	PMID:25512002	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-05-19]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0003701	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0001257	PMID:25512002	PCS		1/1			P	HPO:skoehler[2015-06-22]
OMIM:251950	Mitochondrial myopathy with lactic acidosis		HP:0003128	PMID:25512002	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:226500	Epidermolysis bullosa dystrophica neurotrophica		HP:0002164	OMIM:226500	IEA					P	HPO:iea[2009-02-17]
OMIM:226500	Epidermolysis bullosa dystrophica neurotrophica		HP:0000007	OMIM:226500	IEA					I	HPO:iea[2009-02-17]
OMIM:226500	Epidermolysis bullosa dystrophica neurotrophica		HP:0008404	OMIM:226500	TAS					P	HPO:skoehler[2013-05-03]
OMIM:226500	Epidermolysis bullosa dystrophica neurotrophica		HP:0008527	OMIM:226500	IEA					P	HPO:iea[2009-02-17]
OMIM:226500	Epidermolysis bullosa dystrophica neurotrophica		HP:0007504	OMIM:226500	IEA					P	HPO:iea[2009-02-17]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0003596	PMID:28644393	PCS		5/8			C	HPO:probinson[2022-04-12]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0003584	PMID:28644393	PCS		2/8			C	HPO:probinson[2022-04-12]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0011462	PMID:28644393	PCS		1/8			C	HPO:probinson[2022-04-12]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0007663	PMID:28644393	PCS		8/8			P	HPO:probinson[2022-04-12]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0000603	OMIM:616152	TAS					P	HPO:skoehler[2015-09-15]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0007677	PMID:25085631	PCS		1/2			P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0007754	PMID:25085631	PCS		1/2			P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0000006	PMID:25085631	PCS					I	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616152	Macular dystrophy, vitelliform, 5		HP:0030515	PMID:25085631	PCS		1/2			P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001771	PMID:27745833	PCS		2/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0005216	PMID:27745833	PCS		2/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003577	PMID:27745833	PCS		1/9			C	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003236	PMID:10655510	PCS		4/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0002783	PMID:27745833	PCS		4/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0020152	PMID:10655510	PCS		2/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003551	PMID:10655510	PCS		8/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003691	PMID:10655510	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003593	PMID:27745833	PCS		2/9			C	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003690	PMID:27745833	PCS		9/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003391	PMID:27745833	PCS		4/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0009183	PMID:27745833	PCS		2/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0011463	PMID:27745833	PCS		2/9			C	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0009046	PMID:10655510	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000218	PMID:10655510	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0002359	PMID:27745833	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001324	PMID:27745833	PCS		9/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003701	PMID:27745833	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001763	PMID:10655510	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003306	PMID:10655510	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000577	PMID:27745833	PCS		1/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003700	PMID:27745833	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001265	PMID:27745833	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0002058	PMID:27745833	PCS		9/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003687	PMID:27745833	PCS		5/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0002015	PMID:27745833	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003621	PMID:27745833	PCS		4/9			C	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000098	PMID:27745833	PCS		4/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0002650	PMID:10655510	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003388	PMID:27745833	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000276	PMID:27745833	PCS		4/9			P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001761	PMID:10655510	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001382	PMID:27745833	PCS		4/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0002792	PMID:27745833	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001284	PMID:27745833	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0002091	PMID:27745833	PCS		2/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000508	PMID:10655510	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0030230	PMID:27745833	PCS		5/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000767	PMID:27745833	PCS		2/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000007	PMID:27745833	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000689	PMID:27745833	PCS		2/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001319	PMID:27745833	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001653	PMID:27745833	PCS		1/9			P	HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000347	PMID:10655510	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003798	PMID:27745833	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0003677	PMID:27745833	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0001611	PMID:10655510	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:617258	Myopathy, myofibrillar, 8		HP:0000467	PMID:10655510	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-26]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0003621	PMID:22703882	PCS		2/3			C	HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0011808	PMID:22703882	PCS		1/4			P	HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0003431	PMID:22703882	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0025708	PMID:22703882	PCS		1/3			C	HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0001761	PMID:22703882	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0011727	PMID:22703882	PCS		3/4			P	HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0009049	PMID:22703882	PCS		3/4			P	HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0003393	PMID:22703882	PCS		4/4			P	HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0003438	PMID:22703882	PCS		4/4			P	HPO:probinson[2023-01-15]
OMIM:614751	Neuronopathy, distal hereditary motor, type VB		HP:0000006	PMID:22703882	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-15]
OMIM:614037	Leukotriene C4 synthase deficiency		HP:0000252	PMID:9820300	PCS					P	HPO:probinson[2013-12-15]
OMIM:614037	Leukotriene C4 synthase deficiency		HP:0001531	PMID:9820300	PCS					P	HPO:probinson[2013-12-15]
OMIM:614037	Leukotriene C4 synthase deficiency		HP:0001252	PMID:9820300	PCS					P	HPO:probinson[2013-12-15]
OMIM:614037	Leukotriene C4 synthase deficiency		HP:0001263	PMID:9820300	PCS					P	HPO:probinson[2013-12-15]
OMIM:614037	Leukotriene C4 synthase deficiency		HP:0000007	PMID:9820300	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-01-27]
OMIM:614037	Leukotriene C4 synthase deficiency		HP:0001522	PMID:9820300	PCS					C	HPO:probinson[2013-12-15]
OMIM:614037	Leukotriene C4 synthase deficiency		HP:0030390	PMID:9820300	PCS					P	HP:probinson[2019-01-27]
OMIM:266130	Glutathione synthetase deficiency		HP:0003343	OMIM:266130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:266130	Glutathione synthetase deficiency		HP:0001250	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0410132	PMID:4557757	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:266130	Glutathione synthetase deficiency		HP:0001260	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0001285	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0001251	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0000580	OMIM:266130	TAS					P	HPO:probinson[2015-07-19]
OMIM:266130	Glutathione synthetase deficiency		HP:0002080	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0001878	OMIM:266130	TAS				HP:0012825	P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0000007	OMIM:266130	TAS					I	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0001345	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0001249	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0001996	OMIM:266130	TAS					P	HPO:probinson[2012-06-03]
OMIM:266130	Glutathione synthetase deficiency		HP:0001875	OMIM:266130	TAS				HP:0025303	P	HPO:skoehler[2013-06-10]
OMIM:613758	Retinitis pigmentosa 47		HP:0000662	PMID:9565049	PCS					P	HPO:probinson[2013-06-05]
OMIM:613758	Retinitis pigmentosa 47		HP:0000580	PMID:9565049	PCS					P	HPO:probinson[2017-12-22]
OMIM:613758	Retinitis pigmentosa 47		HP:0000007	PMID:9565049	PCS					I	HPO:probinson[2013-01-09]
OMIM:613758	Retinitis pigmentosa 47		HP:0000505	PMID:9565049	PCS					P	HPO:probinson[2013-06-05]
OMIM:613758	Retinitis pigmentosa 47		HP:0000510	PMID:9565049	PCS					P	HPO:skoehler[2015-01-19]
OMIM:613758	Retinitis pigmentosa 47		HP:0000533	PMID:9565049	PCS					P	HPO:probinson[2013-06-05]
OMIM:613758	Retinitis pigmentosa 47		HP:0000654	PMID:9565049	PCS					P	HPO:probinson[2013-06-05]
OMIM:612446	C6 deficiency		HP:0025434	PMID:32670577	PCS		3/3			P	HPO:probinson[2020-08-13]
OMIM:612446	C6 deficiency		HP:0000007	PMID:32670577	PCS					I	HPO:skoehler[2013-04-06];HPO:probinson[2020-08-13]
OMIM:612446	C6 deficiency		HP:0033059	PMID:32670577	PCS		3/3			P	HPO:probinson[2020-08-13]
OMIM:612446	C6 deficiency		HP:0005381	PMID:32670577	PCS		1/3			P	HPO:skoehler[2013-04-06];HPO:probinson[2020-08-13]
OMIM:191500	Undritz anomaly		HP:0000006	OMIM:191500	IEA					I	HPO:iea[2009-02-17]
OMIM:191500	Undritz anomaly		HP:0004821	OMIM:191500	IEA					P	HPO:iea[2009-02-17]
OMIM:613980	Atrial fibrillation, familial, 9		HP:0004754	PMID:15922306	PCS		2/7			P	HPO:probinson[2022-07-03]
OMIM:613980	Atrial fibrillation, familial, 9		HP:0003596	PMID:15922306	PCS		5/5			C	HPO:probinson[2022-07-03]
OMIM:613980	Atrial fibrillation, familial, 9		HP:0005184	PMID:15922306	PCS		0/7			P	HPO:probinson[2022-07-03]
OMIM:613980	Atrial fibrillation, familial, 9		HP:0001962	PMID:15922306	PCS		4/7			P	HPO:probinson[2022-07-03]
OMIM:613980	Atrial fibrillation, familial, 9		HP:0004757	PMID:15922306	PCS		3/7			P	HPO:skoehler[2013-06-11];HPO:probinson[2022-07-03]
OMIM:613980	Atrial fibrillation, familial, 9		HP:0001279	PMID:15922306	PCS		0/7			P	HPO:probinson[2022-07-03]
OMIM:613980	Atrial fibrillation, familial, 9		HP:0000006	PMID:15922306	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:610251	Alcohol sensitivity, acute		HP:0001033	OMIM:610251	TAS					P	HPO:skoehler[2013-01-09]
OMIM:610251	Alcohol sensitivity, acute		HP:0003533	OMIM:610251	TAS					P	HPO:skoehler[2015-05-03]
OMIM:610251	Alcohol sensitivity, acute		HP:0000006	OMIM:610251	TAS					I	HPO:skoehler[2017-07-13]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0003587	PMID:23455931	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0003676	PMID:23455931	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0002015	PMID:23455931	PCS		4/10			P	HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0002166	PMID:23455931	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0003596	PMID:23455931	PCS		3/10			C	HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0003487	PMID:23455931	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0001761	PMID:23455931	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0000012	PMID:23455931	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0002395	PMID:23455931	PCS		10/10			P	HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0001260	PMID:23455931	PCS		0/10			P	HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0000020	OMIM:603563	IEA					P	HPO:iea[2009-02-17]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0002064	PMID:23455931	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0002061	PMID:23455931	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0007350	PMID:23455931	PCS		8/10			P	HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0007340	PMID:23455931	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0011462	PMID:23455931	PCS		7/10			C	HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0002839	OMIM:603563	IEA					P	HPO:iea[2009-02-17]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0003419	PMID:23455931	PCS		4/10			P	HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0001258	PMID:23455931	PCS		10/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0000006	PMID:17160902	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0006986	OMIM:603563	TAS		HP:0040283			P	HPO:skoehler[2014-02-06]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0002314	OMIM:603563	IEA					P	HPO:iea[2009-02-17]
OMIM:603563	Spastic paraplegia 8, autosomal dominant		HP:0001347	OMIM:603563	IEA					P	HPO:iea[2009-02-17]
OMIM:211390	Sabinas brittle hair syndrome		HP:0002299	OMIM:211390	TAS					P	HPO:skoehler[2012-10-17]
OMIM:211390	Sabinas brittle hair syndrome		HP:0002164	OMIM:211390	IEA					P	HPO:iea[2009-02-17]
OMIM:211390	Sabinas brittle hair syndrome		HP:0000007	OMIM:211390	IEA					I	HPO:iea[2009-02-17]
OMIM:211390	Sabinas brittle hair syndrome		HP:0008404	OMIM:211390	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:211390	Sabinas brittle hair syndrome		HP:0008070	OMIM:211390	IEA					P	HPO:iea[2009-02-17]
OMIM:211390	Sabinas brittle hair syndrome		HP:0001249	OMIM:211390	IEA					P	HPO:iea[2009-02-17]
OMIM:211390	Sabinas brittle hair syndrome		HP:0011359	OMIM:211390	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0001363	PMID:8826432	PCS	HP:0011461	2/2			P	HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0001762	PMID:8826432	PCS	HP:0011461	1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0000193	PMID:8826432	PCS	HP:0011461	1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0007033	PMID:8826432	PCS	HP:0030674	2/2		HP:0012828	P	HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0007265	PMID:8826432	PCS	HP:0030674	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0000007	PMID:8826432	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0007268	PMID:8826432	PCS	HP:0030674	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0007027	PMID:8826432	PCS	HP:0030674	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0007973	PMID:8826432	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-04-16]
OMIM:601374	Aprosencephaly and cerebellar dysgenesis		HP:0000347	PMID:8826432	PCS	HP:0011461	2/2			P	HPO:probinson[2021-04-16]
OMIM:610279	Pachygyria, frontotemporal		HP:0001250	OMIM:610279	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610279	Pachygyria, frontotemporal		HP:0000506	OMIM:610279	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610279	Pachygyria, frontotemporal		HP:0000316	OMIM:610279	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610279	Pachygyria, frontotemporal		HP:0000007	OMIM:610279	IEA					I	HPO:skoehler[2010-06-19]
OMIM:610279	Pachygyria, frontotemporal		HP:0000565	OMIM:610279	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610279	Pachygyria, frontotemporal		HP:0001302	OMIM:610279	IEA					P	HPO:skoehler[2010-06-20]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0003577	PMID:28132691	PCS		3/4			C	HPO:probinson[2022-03-18];HPO:probinson[2022-03-18]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000365	PMID:28132691	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000486	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0002783	PMID:28132691	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-08]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001250	PMID:28132691	PCS		3/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001252	PMID:28132691	PCS		2/3			P	HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000041	PMID:28132691	PCS		1/4	MALE		P	ORCID:0000-0002-0736-9199[2024-07-08]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001270	PMID:28132691	PCS		2/4			P	HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000639	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001629	PMID:28132691	PCS	HP:0003577	1/4			P	HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0100704	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0011463	PMID:28132691	PCS		1/4			C	HPO:probinson[2022-03-18]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000316	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0004736	PMID:28132691	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-08]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001643	PMID:28132691	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000278	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001249	PMID:28132691	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000358	PMID:28132691	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-08]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000054	PMID:28132691	PCS		2/4	MALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001660	PMID:28132691	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000750	PMID:28132691	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0011968	PMID:28132691	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000073	PMID:28132691	PCS		1/4			P	HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001263	PMID:28132691	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0012683	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000729	PMID:28132691	PCS		3/4			P	HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000448	PMID:28132691	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0009777	PMID:28132691	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0001631	PMID:28132691	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-08]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000047	PMID:28132691	PCS		1/4	MALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000960	PMID:28132691	PCS		1/3			P	HPO:probinson[2019-09-02];HPO:probinson[2024-07-08]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0009778	PMID:28132691	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000006	PMID:28132691	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000028	PMID:28132691	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000369	PMID:28132691	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000347	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000324	PMID:28132691	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:617516	Stankiewicz-Isidor syndrome		HP:0000049	PMID:28132691	PCS		1/4	MALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2019-09-02]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0002223	PMID:31303264	PCS		7/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000561	PMID:31303264	PCS		5/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0008209	PMID:31303264	PCS		2/5	FEMALE		P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0004322	PMID:31303264	PCS		6/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0002750	PMID:31303264	PCS		2/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0001263	PMID:31303264	PCS		2/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0008070	PMID:31303264	PCS		7/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000939	PMID:31303264	PCS		1/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0001816	PMID:31303264	PCS		2/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0008066	PMID:31303264	PCS		4/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000957	PMID:31303264	PCS		3/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000007	PMID:31303264	PCS					I	HPO:probinson[2020-06-25];HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0001118	PMID:31303264	PCS	HP:0003621	10/10		HP:0012832	P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000821	PMID:31303264	PCS		2/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000403	PMID:31303264	PCS		2/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0008404	PMID:31303264	PCS		2/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000026	PMID:31303264	PCS		1/5	MALE		P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0001029	PMID:31303264	PCS		10/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000962	PMID:31303264	PCS		4/10			P	HPO:probinson[2020-06-25]
OMIM:618625	Rothmund-thomson syndrome, type 1		HP:0000698	PMID:31303264	PCS		2/10			P	HPO:probinson[2020-06-25]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0008936	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0002421	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0001264	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0003577	PMID:25847581	PCS					C	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0003676	PMID:25847581	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-10]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0000750	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0001344	PMID:25847581	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-10]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0004322	PMID:25847581	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-10]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0001266	PMID:25847581	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-10]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0001263	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0003593	PMID:25847581	PCS		2/2			C	HPO:probinson[2022-04-10]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0011856	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0000718	PMID:25847581	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-10]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0000007	PMID:25847581	PCS					I	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0000733	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0100716	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0001249	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:617270	Intellectual developmental disorder, autosomal recessive 58		HP:0001347	PMID:25847581	PCS		2/2			P	HPO:probinson[2017-06-17]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002069	PMID:33410539	PCS		4/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0030215	PMID:33410539	PCS		1/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000365	PMID:33410539	PCS		2/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002540	PMID:30269814	PCS		4/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002188	PMID:33410539	PCS		1/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001250	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001250	PMID:33410539	PCS	HP:0003593	6/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0003155	PMID:33410539;PMID:30269814	PCS		2/6			P	HPO:probinson[2021-06-27];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001251	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0003593	PMID:33410539	IEA		6/6			C	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001290	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000280	PMID:33410539;PMID:30269814	PCS		9/10			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0012110	PMID:33410539	PCS		4/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000639	PMID:30269814	PCS		3/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0011221	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000954	PMID:30269814	PCS		1/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000158	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002019	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000476	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000358	PMID:30269814	PCS		1/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002553	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000252	PMID:33410539;PMID:30269814	PCS		8/10			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001344	PMID:33410539	PCS		6/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000331	PMID:30269814	PCS		1/5			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0011968	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001382	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001263	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0011927	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0003282	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0010044	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000729	PMID:33410539	PCS		2/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002828	PMID:30269814	PCS		2/6			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0031165	PMID:33410539	PCS		4/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001537	PMID:30269814	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000007	PMID:30269814	PCS					I	HPO:lccarmody[2018-12-18];HP:probinson[2019-01-04]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000768	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0004209	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0007359	PMID:33410539	PCS		3/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000687	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0004689	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000384	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002002	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000023	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001156	PMID:30269814	PCS		3/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001272	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002120	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002240	PMID:30269814	PCS		2/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0100704	PMID:30269814	PCS		3/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0009882	PMID:30269814	PCS		1/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001989	PMID:30269814	PCS		2/6			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000212	PMID:30269814	PCS		3/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0006855	PMID:33410539	PCS		2/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002059	PMID:33410539	PCS		6/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002650	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0003189	PMID:30269814	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002133	PMID:33410539	PCS		5/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001640	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0001288	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000391	PMID:30269814	PCS		4/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0010851	PMID:33410539	PCS		6/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0011344	PMID:33410539	PCS		6/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000748	PMID:33410539	PCS		1/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0002804	PMID:30269814	PCS	HP:0011461	2/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000505	PMID:33410539	PCS		3/6			P	HPO:probinson[2021-06-27]
OMIM:618143	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000028	PMID:30269814	PCS		1/4			P	HPO:lccarmody[2018-12-18];HPO:lccarmody[2018-12-18]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0001276	PMID:18711368;PMID:20956791	PCS	HP:0003577	4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0003577	PMID:18711368;PMID:20956791	PCS		4/4			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0000252	OMIM:225753	IEA					P	HPO:iea[2009-02-17]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0001561	PMID:18711368;PMID:20956791	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0002015	PMID:18711368;PMID:20956791	PCS		4/4			P	HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0001321	OMIM:225753;PMID:20956791	PCS		11/11			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-24];HPO:skoehler[2010-06-18]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0002365	OMIM:225753	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0001250	PMID:20956791	PCS	HP:0003577	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0011968	PMID:20956791	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0002171	PMID:20956791	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0011344	OMIM:225753	TAS					P	HPO:skoehler[2013-06-06]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0012110	PMID:20956791	PCS		1/1			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0007001	PMID:20956791	PCS		1/1			P	HPO:probinson[2013-12-20];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0002803	PMID:18711368;PMID:20956791	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0000007	PMID:18711368	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0002878	PMID:20956791	PCS	HP:0003623	1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0001522	PMID:20956791	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0007105	OMIM:225753	IEA					P	HPO:iea[2009-02-17]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0001257	OMIM:225753	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225753	Pontocerebellar hypoplasia, type 4		HP:0001336	PMID:18711368	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:601412	Deafness, autosomal dominant nonsyndromic sensorineural 7		HP:0005101	OMIM:601412	TAS					P	HPO:probinson[2013-03-24]
OMIM:601412	Deafness, autosomal dominant nonsyndromic sensorineural 7		HP:0000006	OMIM:601412	TAS					I	HPO:probinson[2009-02-17]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0003577	PMID:22577226	PCS		2/2			C	HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0001696	PMID:22577226	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0001651	PMID:22577226	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0003363	OMIM:614779	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0001719	PMID:22577226	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0012020	PMID:22577226	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0001669	PMID:22577226	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0004383	PMID:22577226	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0000007	PMID:22577226	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0011565	PMID:22577226	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0005160	PMID:22577226	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:614779	Heterotaxy, visceral, 6, autosomal		HP:0011579	PMID:22577226	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0002059	PMID:23993195	PCS		2/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0002521	PMID:23993195	PCS		2/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0001344	PMID:23993195	PCS		4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0002540	PMID:23993195	PCS		3/3			P	HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0002188	PMID:23993195	PCS		2/4			P	HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0001332	PMID:23993195	PCS		1/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0002079	PMID:23993195	PCS		2/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0001263	PMID:23993195	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0010818	PMID:23993195	PCS		4/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0003593	PMID:23993195	PCS		2/4			C	HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0002072	PMID:23993195	PCS		1/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0010851	PMID:23993195	PCS		3/4			P	HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0011167	PMID:23993195	PCS		1/4			P	HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0200134	PMID:23993195	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0002305	PMID:23993195	PCS		1/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0000006	PMID:23993195	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-04-11]
OMIM:615473	Developmental and epileptic encephalopathy 17		HP:0003623	PMID:23993195	PCS		2/4			C	HPO:probinson[2023-04-11]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0001254	OMIM:613002	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0001287	PMID:21911422	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0003621	PMID:21911422	PCS		1/1			C	HPO:probinson[2023-01-26]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0001289	PMID:21911422	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0002353	OMIM:613002	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0001250	PMID:21911422	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0002171	OMIM:613002	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0012302	PMID:21911422	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-01-26]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0003829	OMIM:613002	IEA					I	HPO:skoehler[2018-10-08]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0000007	OMIM:613002	IEA					I	HPO:skoehler[2018-10-08]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0001269	OMIM:613002	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0001268	OMIM:613002	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0000006	PMID:17872438	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-26]
OMIM:613002	Immunodeficiency 83, susceptibility to viral infections		HP:0001249	OMIM:613002	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:227150	Ethanolaminosis		HP:0001640	OMIM:227150	IEA					P	HPO:iea[2009-02-17]
OMIM:227150	Ethanolaminosis		HP:0001939	OMIM:227150	IEA					P	HPO:iea[2009-02-17]
OMIM:227150	Ethanolaminosis		HP:0001290	OMIM:227150	IEA					P	HPO:iea[2009-02-17]
OMIM:227150	Ethanolaminosis		HP:0000007	OMIM:227150	IEA					I	HPO:iea[2009-02-17]
OMIM:227150	Ethanolaminosis		HP:0001522	OMIM:227150	IEA					C	HPO:iea[2009-02-17]
OMIM:618157	Growth hormone deficiency, isolated, type IV		HP:0003510	PMID:11232012	PCS		6/6			P	HPO:probinson[2020-07-07]
OMIM:618157	Growth hormone deficiency, isolated, type IV		HP:0010627	PMID:11232012	PCS					P	HPO:probinson[2020-07-07]
OMIM:618157	Growth hormone deficiency, isolated, type IV		HP:0002750	PMID:11232012	PCS					P	HPO:probinson[2020-07-07]
OMIM:618157	Growth hormone deficiency, isolated, type IV		HP:0030353	PMID:11232012	PCS					P	HPO:probinson[2020-07-07]
OMIM:618157	Growth hormone deficiency, isolated, type IV		HP:0000007	PMID:11232012	PCS					I	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618157	Growth hormone deficiency, isolated, type IV		HP:0031079	PMID:11232012	PCS					P	HPO:probinson[2020-07-07]
OMIM:618157	Growth hormone deficiency, isolated, type IV		HP:0000824	PMID:11232012	PCS					P	HPO:probinson[2020-07-07]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0003621	PMID:17036286	PCS		2/6			C	HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0003236	PMID:17036286	PCS		6/6			P	HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0003596	PMID:17036286	PCS		1/6			C	HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0011462	PMID:17036286	PCS		3/6			C	HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0008981	PMID:17036286	PCS		4/6			P	HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0000007	PMID:17036286	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0003391	PMID:17036286	PCS		3/6			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0003701	PMID:17036286	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0012664	PMID:17036286	PCS		6/6			P	HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0033755	PMID:17036286	PCS		6/6			P	HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0001644	PMID:17036286	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:611615	Cardiomyopathy, dilated, 1X		HP:0003557	PMID:17036286	PCS					P	HPO:probinson[2022-07-03]
OMIM:601360	Amelia, autosomal recessive		HP:0009827	OMIM:601360	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601360	Amelia, autosomal recessive		HP:0000007	OMIM:601360	IEA					I	HPO:iea[2009-02-17]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0002069	PMID:11571333;PMID:9012407	PCS		31/32			P	HPO:probinson[2021-07-04];HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0003621	PMID:9012407	PCS		29/29			C	HPO:probinson[2021-06-26]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0001260	OMIM:254800	IEA					P	HPO:iea[2009-02-17]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0002121	OMIM:254800	IEA					P	HPO:iea[2009-02-17]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0001251	PMID:11571333	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0002392	PMID:9012407	PCS					P	HPO:probinson[2021-06-26]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0010850	PMID:11571333	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0011182	PMID:15623692	PCS		6/10			P	HPO:probinson[2021-07-04]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0000726	PMID:11571333	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0000007	PMID:9012407	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0001268	PMID:15623692	PCS		4/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:254800	Epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)		HP:0001336	PMID:11571333;PMID:15623692;PMID:9012407	PCS		42/42			P	HPO:probinson[2021-07-04];HPO:skoehler[2010-06-20];HPO:probinson[2021-06-26]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0003774	OMIM:203780	TAS					P	HPO:skoehler[2012-11-26]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0003676	OMIM:203780	TAS					C	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000365	OMIM:203780	IEA					P	HPO:iea[2009-02-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000123	OMIM:203780	IEA					P	HPO:iea[2009-02-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000100	OMIM:203780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000083	OMIM:203780	IEA					P	HPO:iea[2009-02-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0030034	OMIM:203780	TAS					P	HPO:skoehler[2014-09-21]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000790	OMIM:203780	IEA					P	HPO:iea[2009-02-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0011501	OMIM:203780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000093	OMIM:203780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000518	OMIM:203780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000822	OMIM:203780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000007	OMIM:203780	TAS					I	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0200020	OMIM:203780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0000545	OMIM:203780	TAS					P	HPO:skoehler[2012-10-17]
OMIM:203780	Alport syndrome 2, autosomal recessive		HP:0004722	OMIM:203780	TAS					P	HPO:skoehler[2015-12-30]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0003774	OMIM:219900	IEA					P	HPO:iea[2009-02-17]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0003621	PMID:10444339	PCS		2/2			C	HPO:probinson[2009-02-17];HPO:probinson[2022-04-30]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0007814	PMID:6866439	TAS					P	HPO:probinson[2015-07-19]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0001507	OMIM:219900	IEA					P	HPO:iea[2009-02-17]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0002748	OMIM:219900	IEA					P	HPO:iea[2009-02-17]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent Nephropathic type		HP:0000613	PMID:10444339	PCS		2/2		HP:0012825	P	HPO:probinson[2022-04-30]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0000007	PMID:10444339	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0000093	PMID:10444339	PCS	HP:0003621	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0000488	OMIM:219900	TAS					P	HPO:skoehler[2015-07-26]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0000531	PMID:10444339	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:219900	Cystinosis, late-onset juvenile or adolescent nephropathic		HP:0003358	PMID:10444339	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0001298	OMIM:604218	IEA					P	HPO:skoehler[2015-01-27]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0002059	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0000651	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0001250	OMIM:604218	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0001260	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0002171	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0002071	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0000639	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0000726	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0002529	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0002936	OMIM:604218	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:6001062	PMID:11138927	PCS		2/2			P	HPO:probinson[2024-08-03]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0000006	OMIM:604218	IEA					I	HPO:skoehler[2010-06-19]
OMIM:604218	Encephalopathy, familial, with neuroserpin inclusion bodies		HP:0001336	OMIM:604218	IEA					P	HPO:skoehler[2010-06-19]
OMIM:216400	Cockayne syndrome, type A		HP:0003510	PMID:16865293;PMID:30200888	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0007759	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0003357	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000486	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001376	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0002343	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0004322	PMID:32160415;PMID:16865293	PCS		10/10			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0003278	OMIM:216400	TAS					P	HPO:probinson[2013-04-08]
OMIM:216400	Cockayne syndrome A		HP:0001250	PMID:32160415	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0000083	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000680	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0003273	PMID:32160415	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome, type A		HP:0001252	PMID:30200888	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0001251	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0003593	PMID:32160415;PMID:30200888	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-05-20];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000518	PMID:30200888	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0000958	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000639	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0011461	PMID:32160415	PCS		1/2			C	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0008850	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome, type A		HP:0008897	PMID:30200888	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0001324	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000633	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001249	PMID:32160415	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0005328	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0003469	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000252	PMID:32160415;PMID:16865293;PMID:30200888	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05];ORCID:0000-0002-0736-9199[2024-05-20];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000054	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000970	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0008839	OMIM:216400	TAS					P	HPO:probinson[2013-04-08]
OMIM:216400	Cockayne syndrome A		HP:0005301	PMID:32160415	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000490	PMID:32160415;PMID:16865293;PMID:30200888	PCS		11/12			P	ORCID:0000-0002-0736-9199[2024-05-20];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0001260	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000292	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001263	PMID:32160415;PMID:16865293	PCS		7/7			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0010234	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000093	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome, type A		HP:0034392	PMID:16865293	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0000649	OMIM:216400	TAS					P	HPO:probinson[2012-03-18]
OMIM:216400	Cockayne syndrome A		HP:0000726	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000407	PMID:16865293;PMID:30200888	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05];ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0000448	PMID:16865293;PMID:30200888	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-20];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000007	PMID:16865293	PCS					I	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000689	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000648	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0003758	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000762	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000685	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0002866	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001337	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0002545	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0007814	OMIM:216400;PMID:16865293	PCS		17/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000540	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0002684	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001272	PMID:32160415;PMID:16865293	PCS		7/10			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0001271	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0003130	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0002240	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000580	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0011675	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0008070	OMIM:216400	TAS					P	HPO:skoehler[2013-06-03]
OMIM:216400	Cockayne syndrome A		HP:0011359	OMIM:216400	TAS					P	HPO:skoehler[2013-01-22]
OMIM:216400	Cockayne syndrome A		HP:0001508	PMID:16865293	PCS		8/8			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000858	OMIM:216400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0006297	PMID:32160415	PCS		2/2			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000417	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0002119	PMID:32160415;PMID:16865293	PCS		8/10			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000377	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000135	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001744	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001105	PMID:32160415	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0002135	PMID:16865293	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0003224	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001000	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000670	PMID:16865293;PMID:30200888	PCS		7/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05];ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0002059	PMID:16865293	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000992	PMID:16865293;PMID:30200888	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05];ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:216400	Cockayne syndrome A		HP:0006958	OMIM:216400	TAS					P	HPO:probinson[2012-03-18]
OMIM:216400	Cockayne syndrome A		HP:0001288	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0002808	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0007495	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000987	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0000822	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:216400	Cockayne syndrome A		HP:0001511	PMID:32160415	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000028	PMID:32160415	PCS		1/1	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:216400	Cockayne syndrome A		HP:0000303	OMIM:216400	IEA					P	HPO:iea[2009-02-17]
OMIM:613957	Spermatogenic failure 8		HP:0030974	OMIM:613957	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613957	Spermatogenic failure 8		HP:0000006	OMIM:613957	TAS					I	HPO:skoehler[2019-04-18]
OMIM:613957	Spermatogenic failure 8		HP:0000798	OMIM:613957	TAS					P	HPO:probinson[2020-07-17]
OMIM:613957	Spermatogenic failure 8		HP:0000027	OMIM:613957	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300510	Ovarian dysgenesis 2		HP:0008209	PMID:15136966	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0003621	PMID:15136966	PCS		2/2			C	HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0000013	PMID:15136966	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0000815	PMID:15136966	PCS		2/2			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0000869	OMIM:300510	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300510	Ovarian dysgenesis 2		HP:0000823	PMID:15136966	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0001417	PMID:15136966	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0010464	PMID:15136966	PCS		2/2			P	HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0001007	PMID:15136966	PCS		2/2			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-06-15]
OMIM:300510	Ovarian dysgenesis 2		HP:0000786	PMID:15136966	PCS		2/2			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-06-15]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002322	PMID:16908750	PCS		1/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0007979	PMID:16908750	PCS		4/4		HP:0012825	P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002067	PMID:16908750	PCS		2/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0001332	PMID:16908750	PCS		4/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002066	PMID:16908750	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0008297	OMIM:128230	IEA					P	HPO:skoehler[2010-06-20]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0011463	PMID:7874165	PCS					C	HPO:probinson[2012-07-16];HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0001347	PMID:16908750	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0000473	PMID:16908750	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002311	PMID:16908750	PCS		2/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002356	OMIM:128230	IEA					P	HPO:skoehler[2010-06-20]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002650	OMIM:128230	IEA					P	HPO:iea[2009-02-17]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0001762	OMIM:128230	IEA					P	HPO:iea[2009-02-17]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0003487	PMID:16908750	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0001761	PMID:16908750	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0001260	PMID:16908750	PCS		2/4		HP:0012825	P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002396	PMID:16908750	PCS		1/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002174	OMIM:128230	IEA					P	HPO:iea[2009-02-17]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002075	PMID:16908750	PCS		2/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0033683	PMID:16908750	PCS		2/4			P	HPO:probinson[2021-04-16]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0000007	OMIM:128230	TAS		HP:0040283			I	HPO:skoehler[2012-11-18]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0002548	PMID:16908750	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0001257	PMID:16908750	PCS		1/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0006886	PMID:16908750	PCS		1/4			P	HPO:probinson[2021-02-26]
OMIM:128230	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia		HP:0000006	PMID:7874165	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:212100	Cardioauditory syndrome of sanchez cascos		HP:0005875	OMIM:212100	IEA					P	HPO:iea[2009-02-17]
OMIM:212100	Cardioauditory syndrome of sanchez cascos		HP:0000365	OMIM:212100	IEA					P	HPO:iea[2009-02-17]
OMIM:212100	Cardioauditory syndrome of sanchez cascos		HP:0000007	OMIM:212100	IEA					I	HPO:iea[2009-02-17]
OMIM:212100	Cardioauditory syndrome of sanchez cascos		HP:0001714	OMIM:212100	IEA					P	HPO:iea[2009-02-17]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001254	PMID:33890291;PMID:36190515	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0002267	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001410	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001332	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001250	PMID:33890291;PMID:36190515	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001252	PMID:33890291;PMID:36190515	PCS		4/5			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0012707	PMID:33890291	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0012708	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0003593	PMID:33890291;PMID:36190515	PCS		4/9			C	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0032794	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0003074	PMID:36190515	PCS		5/5			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0011577	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0033725	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0012469	PMID:36190515	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0100247	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000713	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000752	PMID:36190515	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0003228	PMID:33890291	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0003623	PMID:33890291;PMID:36190515	PCS		3/9			C	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0002079	PMID:36190515	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0011968	PMID:33890291;PMID:36190515	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0002033	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0002154	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001263	PMID:33890291;PMID:36190515	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0011448	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0500230	PMID:33890291;PMID:36190515	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000729	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0031165	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000007	PMID:36190515	PCS					I	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000961	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0007359	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0002104	PMID:36190515	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0004887	PMID:36190515	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001259	PMID:36190515	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001336	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0032615	PMID:36190515	PCS		3/3			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001276	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0002521	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0003577	PMID:36190515	PCS		2/6			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000463	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000738	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000737	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001943	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000212	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001942	PMID:33890291	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001347	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0008936	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000194	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001284	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0005484	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0010851	PMID:36190515	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0100710	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0034893	PMID:33890291	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0000268	PMID:33890291	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620423	Multiple mitochondrial dysfunctions syndrome 7		HP:0001873	PMID:36190515	PCS		1/1			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:208158	Arthrogryposis - hyperkeratosis, lethal form		HP:0002804	OMIM:208158	IEA					P	HPO:skoehler[2015-01-19]
OMIM:309520	Lujan-Fryns syndrome		HP:0002002	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001250	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001371	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000460	PMID:17369503	PCS		4/7			P	HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001274	PMID:17369503	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0003593	PMID:17369503	PCS					C	HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001290	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001629	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0011220	OMIM:309520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000718	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000717	OMIM:309520	TAS					P	HPO:skoehler[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000712	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000678	PMID:17369503	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000219	PMID:17369503	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000218	PMID:17369503	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000752	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000256	PMID:17369503	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001249	PMID:17369503	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000275	PMID:17369503	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001166	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000098	PMID:17369503	PCS		3/4			P	HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001187	PMID:17369503	PCS		2/4			P	HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0003189	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000276	PMID:17369503	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000194	PMID:17369503	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001382	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0004970	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000053	PMID:17369503	PCS					P	HPO:probinson[2022-07-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0011304	PMID:17369503	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000709	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0012760	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001519	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001419	PMID:17369503	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000508	PMID:17369503	PCS		2/7			P	HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000426	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000767	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000327	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000722	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000744	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0008544	PMID:17369503	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0002007	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000322	PMID:17369503	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001631	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000446	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000347	PMID:17369503	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0000369	OMIM:309520	IEA					P	HPO:iea[2009-02-17]
OMIM:309520	Lujan-Fryns syndrome		HP:0001611	PMID:17369503	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-17]
OMIM:616185	Ovarian dysgenesis 4		HP:0004325	PMID:25480036	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-06-11]
OMIM:616185	Ovarian dysgenesis 4		HP:0003621	PMID:25480036	PCS		3/3			C	HPO:probinson[2022-06-11];HPO:probinson[2022-06-11]
OMIM:616185	Ovarian dysgenesis 4		HP:0002750	PMID:25480036	PCS		3/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-06-11]
OMIM:616185	Ovarian dysgenesis 4		HP:0004322	PMID:25480036	PCS		4/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-06-11]
OMIM:616185	Ovarian dysgenesis 4		HP:0008232	PMID:25480036	PCS		3/3			P	HPO:probinson[2022-06-11]
OMIM:616185	Ovarian dysgenesis 4		HP:0000007	PMID:25480036	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-11]
OMIM:616185	Ovarian dysgenesis 4		HP:0008214	PMID:25480036	PCS		3/3			P	HPO:probinson[2022-06-11]
OMIM:616185	Ovarian dysgenesis 4		HP:0000786	PMID:25480036	PCS		5/5			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-06-11]
OMIM:300262	X-LINKED intellectual disability, Abidi type		HP:0001249	OMIM:300262	IEA					P	HPO:skoehler[2015-01-27]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0002069	PMID:9430594	PCS		11/12			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-20]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0002411	OMIM:121200	TAS					P	HPO:skoehler[2010-06-18]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0002266	OMIM:121200	TAS					P	HPO:probinson[2009-02-17]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0002373	PMID:9430594	PCS		3/12			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-20]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0001263	OMIM:121200	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0001270	OMIM:121200	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0000006	PMID:9430594	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-20]
OMIM:121200	Seizures, benign familial neonatal, 1		HP:0003623	PMID:9430594	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0007181	OMIM:607088	IEA					P	HPO:iea[2009-02-17]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0003445	OMIM:607088	IEA					P	HPO:iea[2009-02-17]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0009053	OMIM:607088	TAS					P	HPO:probinson[2012-07-22]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0003693	OMIM:607088	TAS					P	HPO:probinson[2012-07-22]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0002792	OMIM:607088	TAS					P	HPO:probinson[2012-07-22]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0009113	OMIM:607088	TAS					P	HPO:probinson[2009-02-17]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0000007	OMIM:607088	IEA					I	HPO:iea[2009-02-17]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0003307	OMIM:607088	IEA					P	HPO:iea[2009-02-17]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0007269	OMIM:607088	TAS					P	HPO:probinson[2009-02-17]
OMIM:607088	Spinal muscular atrophy, distal, autosomal recessive, 3		HP:0003677	OMIM:607088	IEA					C	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002663	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002982	OMIM:600081	TAS					P	HPO:probinson[2012-05-01]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0003698	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0003013	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002980	OMIM:600081	TAS					P	HPO:probinson[2012-05-01]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0003155	PMID:15128933	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0001252	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0003593	OMIM:600081	IEA					C	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0001290	OMIM:600081	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0010502	OMIM:600081	TAS					P	HPO:probinson[2012-05-01]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0001508	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0011463	PMID:15128933	PCS		1/1			C	HPO:probinson[2022-12-21]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0012053	PMID:15128933	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002979	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002757	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0001324	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002753	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0003029	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0005469	OMIM:600081	IEA					P	HPO:skoehler[2009-07-31]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002653	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002752	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0000893	OMIM:600081	TAS					P	HPO:probinson[2012-05-26]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0001288	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0003025	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0003020	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0004492	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002748	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0000007	PMID:15128933	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0000920	OMIM:600081	TAS					P	HPO:probinson[2012-05-26]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002901	PMID:15128933	PCS		1/1			P	HPO:probinson[2022-12-21]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002007	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0001510	OMIM:600081	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0000886	OMIM:600081	IEA					P	HPO:iea[2009-02-17]
OMIM:600081	Vitamin D hydroxylation-deficient rickets, type 1B		HP:0002148	PMID:15128933	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:168600	Parkinson disease, late-onset		HP:0002322	OMIM:168600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0003676	OMIM:168600	TAS					C	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0002067	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0001332	OMIM:168600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0002063	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0012332	OMIM:168600	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:168600	Parkinson disease, late-onset		HP:0000716	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0000738	OMIM:168600	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:168600	Parkinson disease, late-onset		HP:0031908	OMIM:168600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:168600	Parkinson disease, late-onset		HP:0003745	OMIM:168600	TAS					I	HPO:skoehler[2015-12-30]
OMIM:168600	Parkinson disease, late-onset		HP:0001621	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0002019	OMIM:168600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0000751	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0003587	OMIM:168600	TAS					C	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0002015	OMIM:168600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0001300	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0000298	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0000012	OMIM:168600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0001260	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0003584	OMIM:168600	TAS					C	HPO:probinson[2022-04-30]
OMIM:168600	Parkinson disease, late-onset		HP:0003581	OMIM:168600	TAS					C	HPO:probinson[2022-03-21]
OMIM:168600	Parkinson disease, late-onset		HP:0002172	OMIM:168600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:168600	Parkinson disease, late-onset		HP:0011960	OMIM:168600	TAS					P	HPO:skoehler[2012-11-22]
OMIM:168600	Parkinson disease, late-onset		HP:0100315	OMIM:168600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:168600	Parkinson disease, late-onset		HP:0000726	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0002529	OMIM:168600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:168600	Parkinson disease, late-onset		HP:0007311	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:168600	Parkinson disease, late-onset		HP:0000006	OMIM:168600	IEA					I	HPO:skoehler[2019-04-18]
OMIM:168600	Parkinson disease, late-onset		HP:0001337	OMIM:168600	IEA					P	HPO:iea[2009-02-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001771	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002343	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003273	PMID:26700687	PCS		2/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001252	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001252	PMID:28262468	PCS	HP:0003577	2/2			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001290	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003391	PMID:26700687	PCS		2/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000678	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0020045	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003306	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001488	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003700	PMID:36090556;PMID:26700687	PCS		5/5			P	HPO:probinson[2023-07-17];HPO:probinson[2023-07-17];HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000494	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003687	PMID:28262468	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003324	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002474	PMID:26700687	PCS		2/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003200	PMID:28262468	PCS		0/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000771	PMID:28262468	PCS		2/2			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001662	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000490	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0011923	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0012378	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0008081	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0005180	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0034197	PMID:36090556;PMID:26700687	PCS		3/6			C	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0034671	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000602	PMID:26700687	PCS		2/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000767	PMID:28262468;PMID:26700687	PCS		4/7			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000007	PMID:26700687	PCS					I	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000520	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002943	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001612	PMID:26700687	PCS		2/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001611	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003557	PMID:28262468	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0030799	PMID:28262468	PCS		2/2			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003577	PMID:28262468;PMID:26700687	PCS		5/7			C	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003691	PMID:28262468;PMID:26700687	PCS		2/7			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003690	PMID:26700687	PCS		5/5			P	HPO:probinson[2023-07-17];HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001270	PMID:26700687	PCS		4/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0030319	PMID:28262468;PMID:26700687	PCS		6/7			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000939	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002515	PMID:28262468;PMID:26700687	PCS		4/7			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000218	PMID:28262468;PMID:26700687	PCS		6/7			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003327	PMID:26700687	PCS		5/5			P	HPO:probinson[2023-07-17];HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002359	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001623	PMID:36090556;PMID:26700687	PCS		4/6			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001561	PMID:26700687	PCS		3/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002650	PMID:28262468;PMID:36090556;PMID:26700687	PCS		4/8			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001883	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000431	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000276	PMID:26700687	PCS		2/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000194	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002093	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0008180	PMID:28262468	PCS		2/2			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002808	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000508	PMID:28262468	PCS		2/2			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001558	PMID:36090556;PMID:26700687	PCS		4/6			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0001319	PMID:26700687	PCS		4/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0002007	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0003811	PMID:26700687	PCS		1/5			C	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000664	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0005879	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000347	PMID:26700687	PCS		1/5			P	HPO:probinson[2023-07-17]
OMIM:620351	Congenital myopathy 22A, classic		HP:0000544	PMID:36090556	PCS		1/1			P	HPO:probinson[2023-07-17]
OMIM:607936	Peeling skin syndrome 4		HP:0008064	OMIM:607936	IEA					P	HPO:skoehler[2015-01-27]
OMIM:607936	Peeling skin syndrome 4		HP:0100725	OMIM:607936	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607936	Peeling skin syndrome 4		HP:0040189	OMIM:607936	IEA					P	HPO:skoehler[2015-12-30]
OMIM:607936	Peeling skin syndrome 4		HP:0025092	OMIM:607936	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:607936	Peeling skin syndrome 4		HP:0000007	OMIM:607936	TAS					I	HPO:skoehler[2012-10-17]
OMIM:607936	Peeling skin syndrome 4		HP:0040162	OMIM:607936	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607936	Peeling skin syndrome 4		HP:0008404	OMIM:607936	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:607936	Peeling skin syndrome 4		HP:0000982	OMIM:607936	TAS					P	HPO:skoehler[2015-11-15]
OMIM:607936	Peeling skin syndrome 4		HP:0000962	OMIM:607936	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0008064	PMID:21439540	PCS		7/7			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-16]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0025114	PMID:21439540	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0011463	PMID:21439540	PCS		7/7			C	HPO:probinson[2022-03-16]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0025092	PMID:21439540	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-16]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0000007	PMID:21439540	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-16]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0040162	PMID:21439540	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-03-16]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0010783	PMID:21439540	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-16]
OMIM:613943	Ichthyosis, congenital, autosomal recessive 8		HP:0000962	PMID:21439540	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-16]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003555	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002540	OMIM:256030	IEA					P	HPO:skoehler[2018-10-08]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0030059	OMIM:256030	IEA					P	HPO:skoehler[2018-10-08]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001371	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000160	PMID:17525139	PCS		3/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003593	OMIM:256030	IEA					C	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0012548	PMID:17525139	PCS		3/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003393	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0012036	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003707	PMID:17525139	PCS		3/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000316	OMIM:256030	IEA					P	HPO:skoehler[2019-04-18]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0009027	PMID:17525139	PCS		5/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003307	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003701	OMIM:256030	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003306	OMIM:256030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000478	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001265	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001188	OMIM:256030	IEA					P	HPO:skoehler[2019-04-18]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003202	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003324	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003445	OMIM:256030	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000175	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0011968	OMIM:256030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001260	PMID:17525139	PCS		2/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000007	PMID:10051637	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002747	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001533	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003798	PMID:17525139	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000369	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002104	OMIM:256030	TAS				HP:0012828	P	HPO:skoehler[2013-06-11]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003557	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000343	OMIM:256030	IEA					P	HPO:skoehler[2018-10-08]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003376	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003690	OMIM:256030	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001270	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0030319	PMID:17525139	PCS		6/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001547	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003805	PMID:17525139	PCS	HP:0011462	1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002515	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003803	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0000218	PMID:17525139	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002359	PMID:17525139	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003722	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002058	PMID:17525139;OMIM:256030	PCS		11/17			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001561	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002015	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001883	OMIM:256030	IEA					P	HPO:skoehler[2019-04-18]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002650	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003388	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001288	PMID:17525139	PCS		1/7			P	HPO:probinson[2021-06-24]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001283	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001284	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0008180	OMIM:256030	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002803	OMIM:256030	TAS					P	HPO:probinson[2014-01-01]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001558	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0002804	OMIM:256030	TAS				HP:0012828	P	HPO:skoehler[2014-01-28]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0001319	OMIM:256030	IEA					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003810	OMIM:256030	TAS					P	HPO:iea[2009-02-17]
OMIM:256030	Nemaline myopathy 2, autosomal recessive		HP:0003458	PMID:17525139	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:172880	Pierre Robin syndrome and oligodactyly		HP:0000175	OMIM:172880	IEA					P	HPO:skoehler[2010-06-20]
OMIM:172880	Pierre Robin syndrome and oligodactyly		HP:0000201	OMIM:172880	IEA					P	HPO:iea[2009-02-17]
OMIM:172880	Pierre Robin syndrome and oligodactyly		HP:0000006	OMIM:172880	IEA					I	HPO:iea[2009-02-17]
OMIM:172880	Pierre Robin syndrome and oligodactyly		HP:0000347	OMIM:172880	IEA					P	HPO:iea[2009-02-17]
OMIM:172880	Pierre Robin syndrome and oligodactyly		HP:0009380	OMIM:172880	IEA					P	HPO:iea[2009-02-17]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0000343	OMIM:125700	TAS					P	HPO:probinson[2009-02-17]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0031429	OMIM:125700	TAS					P	HPO:probinson[2021-08-22]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0000938	OMIM:125700	TAS					P	HPO:probinson[2009-02-17]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0003196	OMIM:125700	TAS					P	HPO:probinson[2012-04-25]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0002171	OMIM:125700	TAS					P	HPO:skoehler[2010-06-20]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0000316	OMIM:125700	TAS					P	HPO:probinson[2012-04-25]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0000006	OMIM:125700	TAS					I	HPO:probinson[2012-04-25]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0000863	OMIM:125700	TAS					P	HPO:probinson[2009-02-17]
OMIM:125700	Diabetes insipidus, Neurohypophyseal type		HP:0000445	OMIM:125700	TAS					P	HPO:probinson[2012-04-25]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0008936	PMID:37119330	PCS		2/20			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0000252	PMID:37119330	PCS		1/16			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0000750	PMID:37119330	PCS		0/20			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0002376	PMID:37119330	PCS		0/20			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0002395	PMID:37119330	PCS		20/20			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0001250	PMID:37119330	PCS		4/20			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0002373	PMID:37119330	PCS		2/20			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0001251	PMID:37119330	PCS		0/19			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0003593	PMID:37119330	PCS		5/20			C	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0001270	PMID:37119330	PCS		20/20			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0033725	PMID:37119330	PCS		5/9			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0011463	PMID:37119330	PCS		15/20			C	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0000007	PMID:37119330	PCS					I	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0000009	PMID:37119330	PCS		0/19			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0001511	PMID:37119330	PCS		1/19			P	HPO:probinson[2023-07-15]
OMIM:620379	Spastic paraplegia 89, autosomal recessive		HP:0001258	PMID:37119330	PCS		20/20			P	HPO:probinson[2023-07-15]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0004325	PMID:37943610	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002069	PMID:37943610	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002169	PMID:37943610	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0003376	PMID:37943610	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0004322	PMID:37943610	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001332	PMID:37943610	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001250	PMID:37943610	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002066	PMID:37943610	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001252	PMID:37943610	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001251	PMID:37943610	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0003593	PMID:37943610	PCS		5/5			C	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001270	PMID:37943610	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0012157	PMID:37943610	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000518	PMID:37943610	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002719	PMID:37943610	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000316	PMID:37943610	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000218	PMID:37943610	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001348	PMID:37943610	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000252	PMID:37943610	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000494	PMID:37943610	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002136	PMID:37943610	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002650	PMID:37943610	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001344	PMID:37943610	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000750	PMID:37943610	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001762	PMID:37943610	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002013	PMID:37943610	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0003487	PMID:37943610	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001761	PMID:37943610	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001382	PMID:37943610	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002033	PMID:37943610	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001263	PMID:37943610	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0005280	PMID:37943610	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0011094	PMID:37943610	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000767	PMID:37943610	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000007	PMID:37943610	PCS					I	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002527	PMID:37943610	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0001257	PMID:37943610	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0000049	PMID:37943610	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:621067	Neurodevelopmental disorder with poor growth, absent speech, progressive ataxia, and dysmorphic facies		HP:0002721	PMID:37943610	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-04]
OMIM:614962	Leptin deficiency or dysfunction		HP:0000054	OMIM:614962	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614962	Leptin deficiency or dysfunction		HP:0000771	OMIM:614962	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614962	Leptin deficiency or dysfunction		HP:0002591	PMID:9202122	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-11-26]
OMIM:614962	Leptin deficiency or dysfunction		HP:0003292	PMID:9202122	PCS		2/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-26]
OMIM:614962	Leptin deficiency or dysfunction		HP:0011463	PMID:9202122	PCS		2/2			C	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:614962	Leptin deficiency or dysfunction		HP:0000007	PMID:9202122	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-26]
OMIM:614962	Leptin deficiency or dysfunction		HP:0006532	OMIM:614962	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614962	Leptin deficiency or dysfunction		HP:0008734	OMIM:614962	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614962	Leptin deficiency or dysfunction		HP:0002788	OMIM:614962	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614962	Leptin deficiency or dysfunction		HP:0000135	OMIM:614962	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614962	Leptin deficiency or dysfunction		HP:0001513	PMID:9202122	PCS	HP:0011463	2/2			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-26]
OMIM:614962	Leptin deficiency or dysfunction		HP:0000786	OMIM:614962	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614962	Leptin deficiency or dysfunction		HP:0410018	OMIM:614962	TAS					P	HPO:skoehler[2017-07-13]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0000252	OMIM:225790	IEA					P	HPO:skoehler[2019-04-18]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001561	OMIM:225790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0000175	PMID:20206334	PCS		1/7			P	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0003577	PMID:20206334	PCS		7/7			C	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001883	PMID:20206334	PCS		5/7			P	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001321	OMIM:225790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0002365	PMID:20206334	PCS		2/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001250	OMIM:225790	IEA					P	HPO:skoehler[2018-10-08]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001274	OMIM:225790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001263	OMIM:225790	IEA					P	HPO:skoehler[2018-10-08]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0034392	PMID:20206334	PCS		6/7			P	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0000007	PMID:20206334	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001305	OMIM:225790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0000238	PMID:20206334	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0009004	PMID:20206334	PCS		1/7			P	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0002119	PMID:20206334	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0002304	OMIM:225790	IEA					P	HPO:skoehler[2018-10-08]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001511	OMIM:225790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0000476	PMID:20206334	PCS		1/7			P	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001059	PMID:20206334	PCS		2/7			P	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0002324	PMID:20206334	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0000347	OMIM:225790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0002126	PMID:20206334	PCS		1/7			P	HPO:probinson[2023-03-29]
OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		HP:0001622	OMIM:225790	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0000494	PMID:27736875	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0000364	PMID:27736875	PCS		0/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0012471	PMID:27736875	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0000668	PMID:27736875	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0002209	PMID:27736875	PCS		5/5			P	HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0000007	PMID:27736875	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0010763	PMID:27736875	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0000966	PMID:27736875	PCS		4/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0000300	PMID:27736875	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-25]
OMIM:618180	Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis		HP:0000698	PMID:27736875	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-25]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0000252	PMID:22775483	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0003577	PMID:22775483	PCS					C	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-02]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0000486	PMID:20978018	PCS		2/2			P	HPO:probinson[2019-07-08]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0001344	PMID:22775483	PCS		1/3			P	HPO:probinson[2022-09-02]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0002472	OMIM:608393	IEA					P	HPO:iea[2009-02-17]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0001250	PMID:20978018	PCS		2/2			P	HPO:probinson[2019-07-08]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0001263	PMID:20978018	PCS		2/2			P	HPO:probinson[2019-07-08]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0008551	PMID:20978018	PCS		2/2			P	HPO:probinson[2019-07-08]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0000316	PMID:20978018	PCS		2/2			P	HPO:probinson[2019-07-08]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0000007	PMID:22775483	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:608393	Microcephaly, primary autosomal recessive, 6		HP:0000456	PMID:20978018	PCS		2/2			P	HPO:probinson[2019-07-08]
OMIM:614976	Carpenter syndrome 2		HP:0000286	PMID:23063620	PCS		4/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001696	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000243	PMID:23063620	PCS		2/10			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001651	PMID:23063620	PCS	HP:0003577	2/5			P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0001651	PMID:23063620	PCS		2/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001252	PMID:23063620	PCS		2/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0045075	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0011220	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000954	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000316	PMID:23063620	PCS		4/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0002812	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001643	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000278	OMIM:614976	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0000358	PMID:23063620	PCS		2/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0002553	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000054	PMID:23063620	PCS		1/4			P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0001263	PMID:23063620	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0011927	PMID:23063620	PCS		4/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000294	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0011800	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0010554	OMIM:614976	TAS					P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0010239	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0005180	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0100259	OMIM:614976	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0012385	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0006380	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0100258	PMID:23063620	PCS		3/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0009891	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000407	PMID:23063620	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001537	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000767	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0002705	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000689	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000007	PMID:23063620	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000768	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0004209	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0009933	PMID:23063620	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0008689	PMID:23063620	PCS		2/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000369	PMID:23063620	PCS		3/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000248	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000049	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000582	PMID:23063620	PCS		4/10			P	HPO:probinson[2022-05-08];HPO:skoehler[2013-05-31];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000263	OMIM:614976	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0003577	PMID:23063620	PCS		5/5			C	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001234	PMID:23063620	PCS		2/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000189	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000343	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001156	OMIM:614976	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614976	Carpenter syndrome 2		HP:0000463	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0002121	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001669	PMID:23063620	PCS	HP:0003577	1/5			P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0000579	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000218	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0006136	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0006610	PMID:23063620	PCS		4/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000411	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0002557	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0002558	OMIM:614976	TAS					P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0000973	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001363	OMIM:614976	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614976	Carpenter syndrome 2		HP:0000670	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000431	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001762	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000475	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0031936	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000592	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0000470	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0005280	PMID:23063620	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0011304	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0009110	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0007651	PMID:23063620	PCS		1/5			P	HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0002007	OMIM:614976	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0000465	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001631	PMID:23063620	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:614976	Carpenter syndrome 2		HP:0001513	OMIM:614976	TAS					P	HPO:skoehler[2013-05-03]
OMIM:614976	Carpenter syndrome 2		HP:0000028	PMID:23063620	PCS		2/4			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-08]
OMIM:229800	Fructosuria, essential		HP:0011033	OMIM:229800	TAS					P	HPO:iea[2015-04-18]
OMIM:229800	Fructosuria, essential		HP:0000007	PMID:7833921	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-08-03]
OMIM:229800	Fructosuria, essential		HP:6000804	PMID:7833921	PCS		3/3			P	HPO:probinson[2024-08-03]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0007737	PMID:28794130	PCS		4/4			P	HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0000662	PMID:28794130	PCS		4/4			P	HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0007928	PMID:28794130	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0500087	OMIM:618195	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0011463	PMID:28794130	PCS		4/4			C	HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0000608	OMIM:618195	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0000007	PMID:28794130	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0007663	PMID:28794130	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0000543	PMID:28794130	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0007787	PMID:28794130	PCS		1/4			P	HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0007018	PMID:28794130	PCS		3/4			P	HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0007843	PMID:28794130	PCS		4/4			P	HPO:probinson[2022-12-10]
OMIM:618195	Intellectual developmental disorder and retinitis pigmentosa		HP:0001249	PMID:28794130	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-10]
OMIM:243400	Acetylation, slow		HP:0001939	OMIM:243400	IEA					P	HPO:iea[2009-02-17]
OMIM:243400	Acetylation, slow		HP:0000007	OMIM:243400	IEA					I	HPO:iea[2009-02-17]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0003158	PMID:15872203	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0012101	PMID:15872203	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0004421	PMID:15872203	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0031969	PMID:15872203	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0002197	PMID:15872203	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0000737	PMID:15872203	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0001419	PMID:15872203	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0003351	PMID:15872203	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0003593	PMID:15872203	PCS		2/2			C	HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0002902	PMID:15872203	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0012605	PMID:15872203	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:300539	Nephrogenic syndrome of inappropriate antidiuresis		HP:0040085	PMID:15872203	PCS		0/2			P	HPO:probinson[2023-02-18]
OMIM:616806	Wilms tumor 6		HP:0003621	PMID:26551668	PCS		1/18			C	HPO:probinson[2021-02-28]
OMIM:616806	Wilms tumor 6		HP:0011463	PMID:26551668	PCS		13/18			C	HPO:probinson[2021-02-28]
OMIM:616806	Wilms tumor 6		HP:0003593	PMID:26551668	PCS		4/18			C	HPO:probinson[2021-02-28]
OMIM:616806	Wilms tumor 6		HP:0002667	PMID:26551668	PCS					P	HPO:probinson[2017-06-18]
OMIM:616806	Wilms tumor 6		HP:0000006	PMID:26551668	PCS					I	HPO:probinson[2021-02-28]
OMIM:247100	Urbach-Wiethe disease		HP:0003577	PMID:12603844	IEA		3/8			C	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0002232	OMIM:247100	TAS					P	HPO:skoehler[2013-05-03]
OMIM:247100	Urbach-Wiethe disease		HP:0002354	OMIM:247100	IEA					P	HPO:iea[2009-02-17]
OMIM:247100	Urbach-Wiethe disease		HP:0001250	PMID:12603844	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0002121	PMID:12603844	PCS		1/10			P	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0005671	OMIM:247100	IEA					P	HPO:iea[2009-02-17]
OMIM:247100	Urbach-Wiethe disease		HP:0003593	PMID:12603844	PCS		3/8			C	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:6000656	PMID:26803878	PCS					P	HPO:probinson[2024-04-03]
OMIM:247100	Urbach-Wiethe disease		HP:0011999	OMIM:247100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:247100	Urbach-Wiethe disease		HP:0001072	PMID:12603844	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-14];HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:6000842	PMID:26655007	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:247100	Urbach-Wiethe disease		HP:0100699	PMID:12603844	PCS		9/10			P	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0034293	PMID:12603844	PCS		3/10			P	HPO:probinson[2022-09-05]
OMIM:247100	Urbach-Wiethe disease		HP:0000738	OMIM:247100	TAS					P	HPO:skoehler[2013-05-03]
OMIM:247100	Urbach-Wiethe disease		HP:0034760	PMID:15265527	PCS					P	HPO:probinson[2023-06-05]
OMIM:247100	Urbach-Wiethe disease		HP:0008066	PMID:12603844	PCS		1/10			P	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0011463	PMID:12603844	PCS		2/8			C	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0000718	OMIM:247100	TAS					P	HPO:skoehler[2013-05-03]
OMIM:247100	Urbach-Wiethe disease		HP:0001609	PMID:12603844	PCS	HP:0003593	10/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-07-14];HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0000007	PMID:11929856	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-14]
OMIM:247100	Urbach-Wiethe disease		HP:0200035	PMID:12603844	PCS		1/10			P	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0200034	PMID:12603844	PCS		7/10			P	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0000962	PMID:12603844	PCS		1/10			P	HPO:probinson[2022-06-17]
OMIM:247100	Urbach-Wiethe disease		HP:0200041	PMID:12603844	PCS		1/10			P	HPO:probinson[2022-06-17]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001177	PMID:18000979	PCS		1/3			P	HPO:probinson[2023-06-08]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001199	OMIM:174200	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0003577	PMID:18000979;PMID:22428873;PMID:9042919	PCS		21/21			C	HPO:probinson[2023-06-08];HPO:probinson[2023-06-08];HPO:probinson[2024-03-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0002023	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0002164	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001162	PMID:18000979;PMID:22428873;PMID:9042919	PCS		21/21			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-08];HPO:probinson[2023-06-08];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001263	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0010621	PMID:18000979;PMID:22428873	PCS		6/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0010554	PMID:18000979;PMID:22428873	PCS		6/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0011304	PMID:22428873	PCS		6/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2024-03-23]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0100258	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0010055	PMID:22428873	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0006042	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0000316	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001830	PMID:9042919	PCS		11/11			P	HPO:probinson[2023-06-08]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001841	PMID:18000979	PCS		2/3			P	HPO:probinson[2023-06-08]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001159	PMID:9042919	PCS		1/11			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-08]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001510	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0000256	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0000006	PMID:22428873;PMID:9042919	PCS		20/20			I	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-08];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:174200	Polydactyly, postaxial, types A1 and B		HP:0001249	PMID:18000979;PMID:22428873	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:270960	Spermatogenic failure 4		HP:0003251	PMID:14643120	PCS		2/2	MALE		P	HPO:probinson[2022-07-03]
OMIM:270960	Spermatogenic failure 4		HP:0011462	PMID:14643120	PCS		2/2			C	HPO:probinson[2022-07-03]
OMIM:270960	Spermatogenic failure 4		HP:0200067	OMIM:270960	TAS			FEMALE		H	HPO:skoehler[2013-05-31]
OMIM:270960	Spermatogenic failure 4		HP:0000006	PMID:14643120	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-03]
OMIM:270960	Spermatogenic failure 4		HP:0000027	PMID:14643120	PCS		2/2	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-07-03]
OMIM:400004	RETINITIS PIGMENTOSA, Y-LINKED		HP:0000510	OMIM:400004	TAS					P	HPO:skoehler[2017-07-13]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001265	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003378	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003202	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003477	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003376	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003474	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003383	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001284	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003690	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0011096	PMID:11533914	PCS					P	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0011462	PMID:11533914	PCS					C	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0000006	PMID:11533914	PCS					I	HPO:probinson[2023-07-16]
OMIM:620378	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003677	PMID:11533914	PCS					C	HPO:probinson[2023-07-16];HPO:probinson[2023-07-16]
OMIM:139300	Aromatase excess syndrome		HP:0000771	OMIM:139300	TAS					P	HPO:probinson[2009-02-17]
OMIM:139300	Aromatase excess syndrome		HP:0004322	OMIM:139300	TAS					P	HPO:probinson[2013-02-23]
OMIM:139300	Aromatase excess syndrome		HP:0005616	OMIM:139300	TAS					P	HPO:probinson[2013-02-23]
OMIM:139300	Aromatase excess syndrome		HP:0000006	OMIM:139300	TAS					I	HPO:probinson[2013-02-23]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003202	OMIM:616812	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003621	PMID:26642364	PCS		1/3			C	HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003236	PMID:26642364	PCS		2/3			P	HPO:probinson[2017-06-17];HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003687	PMID:26642364	PCS		1/1			P	HPO:probinson[2017-06-17];HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003596	PMID:26642364	PCS		1/3			C	HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0001288	OMIM:616812	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0011706	PMID:26642364	PCS		3/3			P	HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003560	PMID:26642364	PCS					P	HPO:probinson[2017-06-17]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003690	PMID:26642364	PCS		1/3			P	HPO:probinson[2017-06-17];HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0025708	PMID:26642364	PCS		1/3			C	HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0000007	PMID:26642364	PCS					I	HPO:probinson[2017-06-17]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0002505	PMID:26642364	PCS					P	HPO:probinson[2017-06-17]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003701	OMIM:616812	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0001962	OMIM:616812	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0001279	PMID:26642364	PCS		3/3			P	HPO:probinson[2017-06-17];HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003713	PMID:26642364	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003325	PMID:26642364	PCS		1/3			P	HPO:probinson[2017-06-17];HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0001688	PMID:26642364	PCS		1/3			P	HPO:probinson[2017-06-17];HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003326	OMIM:616812	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003557	PMID:26642364	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:616812	Muscular dystrophy, limb-girdle, autosomal recessive 25		HP:0003546	PMID:26642364	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:170700	Peripheral dysostosis		HP:0010230	OMIM:170700	IEA					P	HPO:iea[2009-02-17]
OMIM:170700	Peripheral dysostosis		HP:0008843	OMIM:170700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:170700	Peripheral dysostosis		HP:0000006	OMIM:170700	IEA					I	HPO:iea[2009-02-17]
OMIM:170700	Peripheral dysostosis		HP:0009803	OMIM:170700	IEA					P	HPO:iea[2009-02-17]
OMIM:614963	Leptin receptor deficiency		HP:0004322	OMIM:614963	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614963	Leptin receptor deficiency		HP:0002591	OMIM:614963	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614963	Leptin receptor deficiency		HP:0003593	PMID:9537324	PCS		3/3			C	HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0012286	OMIM:614963	IEA	HP:0003593	HP:0040280			P	HPO:skoehler[2013-01-11]
OMIM:614963	Leptin receptor deficiency		HP:0000819	OMIM:614963	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:614963	Leptin receptor deficiency		HP:0000815	PMID:9537324	PCS		3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0000718	PMID:9537324	PCS	HP:0003593	3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0000712	PMID:9537324	PCS		3/3			P	HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0000007	PMID:9537324	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0002958	OMIM:614963	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614963	Leptin receptor deficiency		HP:0008245	OMIM:614963	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614963	Leptin receptor deficiency		HP:0100738	PMID:9537324	PCS	HP:0003593	3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0000824	OMIM:614963	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614963	Leptin receptor deficiency		HP:0000823	PMID:9537324	PCS		3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0002788	OMIM:614963	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614963	Leptin receptor deficiency		HP:0001513	PMID:9537324	PCS	HP:0003593	3/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-11-06]
OMIM:614963	Leptin receptor deficiency		HP:0001249	PMID:9537324	PCS		0/3			P	HPO:probinson[2022-11-06]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0001166	PMID:16199551	PCS		1/7			P	HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000582	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000340	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0001176	OMIM:300263	TAS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000175	PMID:17594395;OMIM:300263	PCS		5/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-30];HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000252	PMID:17594395	PCS		1/1			P	HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000750	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000276	PMID:16199551	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0002162	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0010511	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0410030	PMID:17594395;OMIM:300263	PCS		6/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-30];HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0001419	PMID:16497722	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000455	OMIM:300263	TAS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0002942	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000664	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0001763	OMIM:300263	TAS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0000336	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0001249	PMID:17594395	PCS		1/1			P	HPO:probinson[2021-09-30]
OMIM:300263	Intellectual developmental disorder, X-linked syndromic, Siderius type		HP:0001611	OMIM:300263	TAS					P	HPO:skoehler[2017-07-13]
OMIM:121201	Epilepsy, benign neonatal, 2		HP:0002069	PMID:9425900	PCS	HP:0003623	1/7			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:121201	Epilepsy, benign neonatal, 2		HP:0002069	PMID:9425900	PCS		0/15			P	HPO:probinson[2024-03-08]
OMIM:121201	Epilepsy, benign neonatal, 2		HP:0002266	PMID:9425900	PCS		21/22			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:121201	Epilepsy, benign neonatal, 2		HP:0001263	PMID:9425900	PCS		0/15			P	HPO:probinson[2014-05-22];HPO:probinson[2024-03-08]
OMIM:121201	Epilepsy, benign neonatal, 2		HP:0000006	PMID:9425900	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:121201	Epilepsy, benign neonatal, 2		HP:0001249	PMID:9425900	PCS		0/7			P	HPO:probinson[2024-03-08]
OMIM:121201	Epilepsy, benign neonatal, 2		HP:0003623	PMID:9425900	PCS		21/21			C	HPO:probinson[2024-03-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002024	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0025466	PMID:11044475	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003155	PMID:11044475	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003076	PMID:11044475	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002240	PMID:11044475	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003593	PMID:11044475	PCS		1/3			C	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0011998	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003270	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0012202	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0012468	OMIM:227810	TAS					P	HPO:skoehler[2013-11-28]
OMIM:227810	Fanconi-Bickel syndrome		HP:0031964	PMID:11044475	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002919	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0001508	PMID:11044475	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0004915	PMID:11044475	PCS		3/3			P	HPO:probinson[2012-07-27];HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003109	PMID:11044475	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0008897	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0001406	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0001941	OMIM:227810	IEA					P	HPO:skoehler[2010-06-20]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003623	PMID:11044475	PCS		1/3			C	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0031956	PMID:11044475	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0001263	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0004396	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003162	PMID:11044475	PCS		3/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002150	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0030948	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0000093	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0012024	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002909	PMID:11044475	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002904	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002748	PMID:11044475	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0000007	PMID:11044475	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002749	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002900	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003758	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0003537	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0000124	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:227810	Fanconi-Bickel syndrome		HP:0002148	OMIM:227810	IEA					P	HPO:iea[2009-02-17]
OMIM:300505	Intellectual developmental disorder, X-linked 84		HP:0004322	OMIM:300505	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300505	Intellectual developmental disorder, X-linked 84		HP:0001419	OMIM:300505	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300505	Intellectual developmental disorder, X-linked 84		HP:0000337	OMIM:300505	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300505	Intellectual developmental disorder, X-linked 84		HP:0001249	OMIM:300505	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600080	Myelocytic leukemia-like syndrome, familial, chronic		HP:0005506	OMIM:600080	TAS					P	HPO:iea[2009-02-17]
OMIM:600080	Myelocytic leukemia-like syndrome, familial, chronic		HP:0000006	OMIM:600080	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002322	PMID:23526723	PCS		2/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0003676	OMIM:168601	TAS					C	HPO:skoehler[2015-12-30]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002067	PMID:23526723	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0001332	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002362	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002063	PMID:23526723	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002283	PMID:23526723	PCS	HP:0003584	2/3			P	HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0000716	OMIM:168601	TAS					P	HPO:skoehler[2015-12-30]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0000738	PMID:23526723	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0011462	PMID:23526723	PCS		3/4			C	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0031908	OMIM:168601	IEA					P	HPO:skoehler[2018-10-08]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0001268	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0003587	OMIM:168601	TAS					C	HPO:skoehler[2015-12-30]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002015	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002375	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0001300	PMID:23526723	PCS		4/4			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0001288	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0000012	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0001260	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0003584	PMID:23526723	PCS		1/4			C	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002171	OMIM:168601	IEA					P	HPO:skoehler[2018-10-08]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002172	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0100315	OMIM:168601	IEA					P	HPO:skoehler[2018-10-08]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0000726	OMIM:168601	IEA					P	HPO:skoehler[2018-10-08]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0002505	PMID:23526723	PCS	HP:0003584	4/4			P	HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0000006	PMID:9197268	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-22]
OMIM:168601	Parkinson disease 1, autosomal dominant		HP:0001336	OMIM:168601	TAS					P	HPO:skoehler[2015-01-04]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0000750	PMID:16767100	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0002121	PMID:16767100	PCS		2/3			P	HPO:nvasilevsky[2019-03-29];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0010819	PMID:16767100	PCS		1/3			P	HPO:nvasilevsky[2019-03-29];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0030243	PMID:16767100	PCS					P	HPO:nvasilevsky[2019-03-29];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0002240	PMID:16767100	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0030242	PMID:16767100	PCS		2/3			P	HPO:skoehler[2015-01-20];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0005561	PMID:16767100	PCS		0/3			P	HPO:nvasilevsky[2019-03-29];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0003593	PMID:16767100	PCS		2/3			C	HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0031555	PMID:17442906	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0001409	PMID:16767100	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0011463	PMID:16767100	PCS		1/3			C	HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0000007	PMID:16767100	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0004936	PMID:16767100	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-27]
OMIM:610293	Glycosylphosphatidylinositol deficiency		HP:0001744	PMID:16767100	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-27]
OMIM:618803	Respiratory papillomatosis, juvenile recurrent, congenital		HP:0032152	PMID:31484767	PCS		2/2			P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:618803	Respiratory papillomatosis, juvenile recurrent, congenital		HP:0001609	PMID:31484767	PCS	HP:0003593	2/2			P	HPO:probinson[2020-04-13]
OMIM:618803	Respiratory papillomatosis, juvenile recurrent, congenital		HP:0033001	PMID:31484767	PCS	HP:0003593	2/2			P	HPO:probinson[2020-10-13]
OMIM:618803	Respiratory papillomatosis, juvenile recurrent, congenital		HP:0000007	PMID:31484767	PCS					I	HPO:probinson[2020-04-13];HPO:probinson[2020-04-13]
OMIM:618803	Respiratory papillomatosis, juvenile recurrent, congenital		HP:0100837	PMID:31484767	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:620344	Prolonged electroretinal response suppression 2		HP:0030512	PMID:19818506;PMID:14702087	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620344	Prolonged electroretinal response suppression 2		HP:0030511	PMID:19818506;PMID:14702087;PMID:17698770	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620344	Prolonged electroretinal response suppression 2		HP:0000639	PMID:19818506;PMID:14702087	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620344	Prolonged electroretinal response suppression 2		HP:0011463	PMID:19818506;PMID:14702087;PMID:17698770	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620344	Prolonged electroretinal response suppression 2		HP:0000613	PMID:19818506;PMID:14702087;PMID:17698770	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620344	Prolonged electroretinal response suppression 2		HP:0007663	PMID:19818506;PMID:14702087;PMID:17698770	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620344	Prolonged electroretinal response suppression 2		HP:0000007	PMID:14702087	PCS					I	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:300511	Premature ovarian failure 2A		HP:0008209	PMID:9497258	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-12-03]
OMIM:300511	Premature ovarian failure 2A		HP:0000869	PMID:9497258	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:300511	Premature ovarian failure 2A		HP:0011969	PMID:9497258	PCS		2/2			P	HPO:probinson[2022-12-03]
OMIM:300511	Premature ovarian failure 2A		HP:0011462	PMID:9497258	PCS		2/2			C	HPO:probinson[2022-12-03]
OMIM:300511	Premature ovarian failure 2A		HP:0008232	PMID:9497258	PCS		2/2			P	HPO:probinson[2022-12-03]
OMIM:300511	Premature ovarian failure 2A		HP:0001423	PMID:9497258	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-03]
OMIM:242050	Hypouricemia, hypercalcinuria, and decreased bone density		HP:0000924	OMIM:242050	IEA					P	HPO:iea[2009-02-17]
OMIM:242050	Hypouricemia, hypercalcinuria, and decreased bone density		HP:0000007	OMIM:242050	IEA					I	HPO:iea[2009-02-17]
OMIM:242050	Hypouricemia, hypercalcinuria, and decreased bone density		HP:0002150	OMIM:242050	IEA					P	HPO:iea[2009-02-17]
OMIM:242050	Hypouricemia, hypercalcinuria, and decreased bone density		HP:0003537	OMIM:242050	IEA					P	HPO:iea[2009-02-17]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0002014	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0002013	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0011968	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0002153	PMID:9662404	PCS		5/5			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-03-23]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0001508	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0000859	PMID:9662404	PCS					P	HPO:skoehler[2012-10-12];HPO:probinson[2022-03-23]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0000848	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0008242	PMID:9662404	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-03-23]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0001944	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0002902	PMID:9662404	PCS		3/5			P	HPO:skoehler[2012-10-12];HPO:probinson[2022-03-23]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0002615	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0000006	PMID:9662404	PCS					I	HPO:skoehler[2012-10-12];HPO:probinson[2022-03-23]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0001942	OMIM:177735	TAS					P	HPO:skoehler[2012-10-12]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0000841	OMIM:177735	TAS					P	HPO:skoehler[2013-06-13]
OMIM:177735	Pseudohypoaldosteronism, type I, autosomal dominant		HP:0003623	PMID:9662404	PCS					C	HPO:probinson[2022-03-23]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0001056	OMIM:131760	TAS					P	HPO:probinson[2009-02-17]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0003577	PMID:10730767;PMID:1717157	PCS		2/5			C	HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0001075	OMIM:131760	TAS		HP:0040283			P	HPO:skoehler[2015-02-15]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0034067	PMID:10730767;PMID:1717157	PCS		5/6			P	HPO:probinson[2022-05-16];HPO:probinson[2022-03-21];HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0008066	PMID:10730767;PMID:1717157	PCS		7/7		HP:0025295;HP:0025295	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-16];HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0011463	PMID:1717157	PCS		2/4			C	HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0001609	PMID:10730767	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0001615	PMID:10730767	PCS		1/1			P	HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0008404	PMID:10730767	PCS		1/1			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0000972	OMIM:131760	TAS					P	HPO:probinson[2009-02-17]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0001510	OMIM:131760	TAS					P	HPO:skoehler[2010-06-18]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0000006	PMID:1717157	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0034193	PMID:10730767;PMID:1717157	PCS		7/7			P	HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0200097	PMID:10730767	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-16]
OMIM:131760	Epidermolysis bullosa simplex, Dowling-Meara type		HP:0003623	PMID:1717157	PCS		1/4			C	HPO:probinson[2015-02-15];HPO:probinson[2022-05-16]
OMIM:613956	Candidiasis, familial, 6, autosomal dominant		HP:0002728	PMID:21350122	PCS					P	HPO:probinson[2013-01-09]
OMIM:613956	Candidiasis, familial, 6, autosomal dominant		HP:0000006	PMID:21350122	PCS					I	HPO:probinson[2013-08-10]
OMIM:231900	Hemolytic anemia due to glutathione synthetase deficiency		HP:0003258	OMIM:231900	TAS					P	HPO:probinson[2009-02-17]
OMIM:231900	Hemolytic anemia due to glutathione synthetase deficiency		HP:0003343	PMID:3944259;PMID:8896573	PCS		6/6			P	HPO:probinson[2012-06-03];HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:231900	Hemolytic anemia due to glutathione synthetase deficiency		HP:0410132	PMID:8896573	PCS		4/4			P	HPO:probinson[2022-12-18]
OMIM:231900	Hemolytic anemia due to glutathione synthetase deficiency		HP:0001878	PMID:3944259;PMID:8896573	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18];HPO:probinson[2022-12-18]
OMIM:231900	Hemolytic anemia due to glutathione synthetase deficiency		HP:0000007	PMID:8896573	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:231900	Hemolytic anemia due to glutathione synthetase deficiency		HP:0001249	PMID:3944259;PMID:8896573	PCS		2/4			P	HPO:probinson[2022-12-18]
OMIM:231900	Hemolytic anemia due to glutathione synthetase deficiency		HP:0001942	PMID:3944259;PMID:8896573	PCS		2/4			P	HPO:probinson[2022-12-18]
OMIM:620422	Retinitis pigmentosa 97		HP:0001089	PMID:37012052	PCS		1/11			P	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0003621	PMID:37012052	PCS		5/9			C	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0000662	PMID:37012052	PCS		11/11			P	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0011463	PMID:37012052	PCS		4/9			C	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0000608	PMID:37012052	PCS		11/11			P	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0000646	PMID:37012052	PCS		2/11			P	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0007663	PMID:37012052	PCS		11/11			P	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0000510	PMID:37012052	PCS		11/11			P	HPO:probinson[2024-02-15]
OMIM:620422	Retinitis pigmentosa 97		HP:0000006	PMID:37012052	PCS					I	HPO:probinson[2024-02-15]
OMIM:619248	Vitreoretinopathy with phalangeal epiphyseal dysplasia		HP:0005920	PMID:12205109	PCS					P	HPO:probinson[2021-05-11]
OMIM:619248	Vitreoretinopathy with phalangeal epiphyseal dysplasia		HP:0001156	PMID:12205109	PCS					P	HPO:probinson[2021-05-11]
OMIM:619248	Vitreoretinopathy with phalangeal epiphyseal dysplasia		HP:0004322	PMID:12205109	PCS		0/2			P	HPO:probinson[2021-05-11];HPO:probinson[2024-03-16]
OMIM:619248	Vitreoretinopathy with phalangeal epiphyseal dysplasia		HP:0012230	PMID:12205109	PCS					P	HPO:probinson[2021-05-11]
OMIM:619248	Vitreoretinopathy with phalangeal epiphyseal dysplasia		HP:0007992	PMID:12205109	PCS					P	HPO:probinson[2021-05-11]
OMIM:619248	Vitreoretinopathy with phalangeal epiphyseal dysplasia		HP:0008843	PMID:12205109	PCS					P	HPO:probinson[2021-05-11]
OMIM:619248	Vitreoretinopathy with phalangeal epiphyseal dysplasia		HP:0000006	PMID:12205109	PCS					I	HPO:probinson[2021-05-11];HPO:probinson[2021-05-11]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0002014	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0001399	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0003256	OMIM:235555	TAS					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0003155	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0002240	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0002570	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0001508	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0002904	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0000007	OMIM:235555	IEA					I	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0001406	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0002910	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0000952	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0001744	OMIM:235555	IEA					P	HPO:iea[2009-02-17]
OMIM:235555	Bile acid synthesis defect, congenital, 2		HP:0003623	OMIM:235555	IEA					C	HPO:iea[2009-02-17]
OMIM:608345	Nystagmus 3, congenital, autosomal dominant		HP:0003577	PMID:9806847	PCS		3/3			C	HPO:probinson[2022-09-02];HPO:probinson[2024-03-13]
OMIM:608345	Nystagmus 3, congenital, autosomal dominant		HP:0007286	PMID:9806847	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-13]
OMIM:608345	Nystagmus 3, congenital, autosomal dominant		HP:0007663	PMID:9806847	PCS		0/3			P	HPO:probinson[2024-03-13]
OMIM:608345	Nystagmus 3, congenital, autosomal dominant		HP:0000006	PMID:9806847	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-13]
OMIM:618156	Squalene synthase deficiency		HP:0000286	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0001531	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0001250	PMID:29909962	PCS	HP:0003623	3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:6000675	PMID:29909962	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:618156	Squalene synthase deficiency		HP:0033146	PMID:29909962	PCS					P	HPO:probinson[2020-10-13]
OMIM:618156	Squalene synthase deficiency		HP:0000958	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000737	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0100704	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0001647	PMID:29909962	PCS		1/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0009887	PMID:29909962	PCS					P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000278	PMID:29909962	PCS		2/3		HP:0012825	P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0002019	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000358	PMID:29909962	PCS		1/3			P	HPO:probinson[2023-02-11]
OMIM:618156	Squalene synthase deficiency		HP:0000992	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0003563	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0002079	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0003146	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:6000465	PMID:29909962	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:618156	Squalene synthase deficiency		HP:0003100	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:6000147	PMID:32027475	PCS					P	HPO:probinson[2024-01-13]
OMIM:618156	Squalene synthase deficiency		HP:6000466	PMID:29909962	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:618156	Squalene synthase deficiency		HP:0004691	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0012736	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0005280	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0011471	PMID:29909962	PCS		3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0033083	PMID:29909962	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618156	Squalene synthase deficiency		HP:0000609	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0006380	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000007	PMID:29909962	PCS					I	HPO:probinson[2020-07-10];HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000400	PMID:29909962	PCS		2/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0001511	PMID:29909962	PCS	HP:0030674	3/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0008689	PMID:29909962	PCS		1/2	MALE		P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000047	PMID:29909962	PCS		1/2	MALE		P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0002987	PMID:29909962	PCS		1/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0002126	PMID:29909962	PCS		1/3			P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000347	PMID:29909962	PCS		2/3		HP:0012825	P	HPO:probinson[2020-07-10]
OMIM:618156	Squalene synthase deficiency		HP:0000369	PMID:29909962	PCS		1/3			P	HPO:probinson[2023-02-11]
OMIM:613003	Attention deficit-hyperactivity disorder, susceptibility to, 7		HP:0000716	PMID:18347598	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:613003	Attention deficit-hyperactivity disorder, susceptibility to, 7		HP:0001263	PMID:18347598	PCS		0/2			P	HPO:probinson[2022-08-27]
OMIM:613003	Attention deficit-hyperactivity disorder, susceptibility to, 7		HP:0007018	PMID:18347598	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:613003	Attention deficit-hyperactivity disorder, susceptibility to, 7		HP:0000006	PMID:18347598	PCS					I	HPO:probinson[2022-08-27]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000055	PMID:19889212	PCS		0/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0031923	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000494	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0003577	PMID:19889212	PCS		1/2			C	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000013	OMIM:277000	IEA					P	HPO:iea[2009-02-17]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0005565	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000151	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0003250	PMID:19889212	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0012673	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0034197	PMID:19889212	PCS		1/2			C	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0033131	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000107	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0031909	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000147	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000003	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000006	OMIM:277000	IEA					I	HPO:iea[2009-02-17]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0005338	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09]
OMIM:277000	Mayer-Rokitansky-Kuster-Hauser syndrome		HP:0000786	PMID:19889212	PCS		1/2			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:615314	Craniosynostosis 3		HP:0000486	PMID:23354436	PCS		11/72			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0001156	PMID:23354436	PCS		4/72			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0004442	PMID:23354436	PCS	HP:0003577	4/72			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0000294	PMID:23354436	PCS		9/72			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0011318	PMID:23354436	PCS	HP:0003577	25/72			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0011317	PMID:23354436	PCS	HP:0003577	18/72			P	HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0011316	PMID:23354436	PCS	HP:0003577	5/72			P	HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0011342	PMID:23354436	PCS		2/72			P	HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0000508	PMID:23354436	PCS		3/72			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0000717	PMID:23354436	PCS		2/72			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0000954	PMID:23354436	PCS		8/72			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0001822	PMID:23354436	PCS		7/72			P	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0000689	PMID:23354436	PCS		7/72			P	HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0001338	PMID:23354436	PCS		2/72			P	HPO:probinson[2022-03-07]
OMIM:615314	Craniosynostosis 3		HP:0000006	PMID:23354436	PCS					I	HPO:skoehler[2013-09-17];HPO:probinson[2022-03-07]
OMIM:602668	Dystrophia myotonica 2		HP:0003554	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0003236	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0003596	PMID:18057971	PCS		1/1			C	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0002486	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0030891	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0011712	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0030319	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0012036	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0008232	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0001649	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0001962	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0007787	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0003701	PMID:18057971	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0000135	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0001249	PMID:18057971	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0000798	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0004315	PMID:18057971	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0003700	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0007889	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0003326	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0003722	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0002850	OMIM:602668	TAS					P	HPO:skoehler[2013-03-13]
OMIM:602668	Dystrophia myotonica 2		HP:0001265	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0002292	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0012899	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0008189	OMIM:602668	IEA					P	HPO:iea[2009-02-17]
OMIM:602668	Dystrophia myotonica 2		HP:0006682	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0005978	PMID:18057971	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:602668	Dystrophia myotonica 2		HP:0000006	PMID:11486088	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:604219	Cataract 9, multiple types		HP:0000486	OMIM:604219	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000482	OMIM:604219	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000518	OMIM:604219	TAS					P	HPO:probinson[2013-09-14]
OMIM:604219	Cataract 9, multiple types		HP:0000639	OMIM:604219	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000519	OMIM:604219	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604219	Cataract 9, multiple types		HP:0000646	OMIM:604219	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000612	OMIM:604219	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000568	OMIM:604219	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000007	OMIM:604219	IEA					I	HPO:skoehler[2018-10-08]
OMIM:604219	Cataract 9, multiple types		HP:0000505	OMIM:604219	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000501	OMIM:604219	TAS					P	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0000006	OMIM:604219	TAS					I	HPO:skoehler[2013-11-18]
OMIM:604219	Cataract 9, multiple types		HP:0007834	OMIM:604219	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:613765	Cardiomyopathy, familial hypertrophic, 9		HP:0001639	PMID:10462489	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-20]
OMIM:613765	Cardiomyopathy, familial hypertrophic, 9		HP:0003581	PMID:10462489	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:613765	Cardiomyopathy, familial hypertrophic, 9		HP:0000006	PMID:10462489	PCS					I	HPO:probinson[2013-06-05];HPO:probinson[2020-09-20]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003687	PMID:23543484	PCS					P	HPO:skoehler[2014-08-03];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003621	PMID:23543484	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0002015	PMID:23543484	PCS		12/32			P	HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0031936	PMID:23543484	PCS		6/32			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003551	PMID:23543484	PCS		19/32			P	HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003581	PMID:23543484	PCS					C	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003691	PMID:23543484	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003560	PMID:23543484	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0002460	PMID:23543484	PCS		24/30			P	HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0001270	PMID:23543484	PCS		5/32			P	HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0100297	PMID:23543484	PCS					P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0034392	PMID:23543484	PCS		2/32			P	HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0009046	PMID:23543484	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0000508	PMID:23543484	PCS		5/32			P	HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003749	PMID:23543484	PCS		32/32			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003805	PMID:23543484	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003736	PMID:23543484	PCS					P	HPO:skoehler[2014-08-03];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0002747	PMID:23543484	PCS		3/32			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003547	PMID:23543484	PCS		32/32			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003306	PMID:23543484	PCS		2/32			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0000006	PMID:23543484	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0003458	PMID:23543484	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608423	Muscular dystrophy, limb-girdle, autosomal dominant 2		HP:0034291	PMID:23543484	PCS		20/20			P	HPO:probinson[2023-02-04]
OMIM:618624	Noonan syndrome 12		HP:0000486	PMID:31130282	PCS		3/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0000540	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001252	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001076	PMID:31130282	PCS		2/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0004381	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001270	PMID:31130282	PCS		2/9		HP:0012825	P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001629	PMID:31130282	PCS		3/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0011342	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0008872	PMID:31130282	PCS		3/6			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001888	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0002119	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0009623	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0000878	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001545	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001561	PMID:31130282	PCS	HP:0011461	3/6			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001047	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001636	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0002308	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0000767	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0000646	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0000824	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0000565	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0003416	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0001873	PMID:31130282	PCS		1/9			P	HPO:probinson[2020-07-14]
OMIM:618624	Noonan syndrome 12		HP:0000006	PMID:31130282	PCS					I	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:109200	Alopecia, androgenetic, 1		HP:0001596	OMIM:109200	TAS					P	HPO:probinson[2009-02-17]
OMIM:109200	Alopecia, androgenetic, 1		HP:0001470	OMIM:109200	IEA					I	HPO:skoehler[2012-10-12]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0000044	PMID:23656588	PCS		1/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0002059	PMID:23656588	PCS		5/10			P	HPO:skoehler[2013-07-30];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0003621	PMID:23656588	PCS		10/12			C	HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0001272	PMID:23656588	PCS		8/10			P	HPO:skoehler[2013-07-30];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0001260	PMID:23656588	PCS		6/12			P	HPO:skoehler[2013-07-30];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0001251	PMID:23656588	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0002072	PMID:23656588	PCS		3/12			P	HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0025708	PMID:23656588	PCS		1/12			C	HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0000639	PMID:23656588	PCS		2/12			P	HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0000726	PMID:23656588	PCS		6/12			P	HPO:skoehler[2013-07-30]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0000869	PMID:23656588	PCS		2/4			P	HPO:probinson[2023-03-15];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0008197	PMID:23656588	PCS		6/12			P	HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0011463	PMID:23656588	PCS		1/12			C	HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0000007	PMID:23656588	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0000876	PMID:23656588	PCS		2/4			P	HPO:skoehler[2013-07-30];HPO:probinson[2023-03-15]
OMIM:212840	Cerebellar ataxia and hypogonadotropic hypogonadism		HP:0000786	PMID:23656588	PCS		1/4			P	HPO:probinson[2023-03-15];HPO:probinson[2023-03-15]
OMIM:615300	Perrault syndrome 4		HP:0008209	OMIM:615300	IEA					P	HPO:skoehler[2013-09-17]
OMIM:615300	Perrault syndrome 4		HP:0000175	PMID:32767731	PCS		1/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000013	PMID:32767731	PCS		5/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000486	PMID:32767731	PCS		1/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0025643	PMID:32767731	PCS		1/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0002066	PMID:32767731	PCS		1/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0001270	PMID:32767731	PCS		2/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000939	PMID:32767731	PCS		1/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0100543	PMID:32767731	PCS		2/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000408	PMID:32767731	PCS	HP:0011463	17/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000837	PMID:32767731	PCS		10/11			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0001519	PMID:32767731	PCS		3/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000869	PMID:32767731	PCS		2/10			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000007	PMID:32767731	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000876	PMID:32767731	PCS		2/10			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000813	PMID:32767731	PCS		1/11			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0008214	PMID:32767731	PCS		3/11			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0002967	PMID:32767731	PCS		1/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0001513	PMID:32767731	PCS		1/17			P	HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0000786	OMIM:615300	IEA		6/10	FEMALE		P	HPO:skoehler[2013-09-17];HPO:probinson[2020-08-10]
OMIM:615300	Perrault syndrome 4		HP:0008724	PMID:32767731	PCS		2/11			P	HPO:probinson[2020-08-10]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0000365	OMIM:144300	IEA					P	HPO:iea[2009-02-17]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0002155	OMIM:144300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0003124	OMIM:144300	IEA					P	HPO:iea[2009-02-17]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0001084	OMIM:144300	IEA					P	HPO:iea[2009-02-17]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0003141	OMIM:144300	IEA					P	HPO:iea[2009-02-17]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0002635	OMIM:144300	IEA					P	HPO:iea[2009-02-17]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0000006	OMIM:144300	IEA					I	HPO:iea[2009-02-17]
OMIM:144300	Hyperlipoproteinemia, type II, and deafness		HP:0000951	OMIM:144300	IEA					P	HPO:iea[2009-02-17]
OMIM:603204	Epilepsy, nocturnal frontal lobe, 2		HP:0002069	OMIM:603204	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:603204	Epilepsy, nocturnal frontal lobe, 2		HP:0000708	OMIM:603204	TAS		12/20			P	HPO:skoehler[2013-01-21]
OMIM:603204	Epilepsy, nocturnal frontal lobe, 2		HP:0002133	OMIM:603204	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:603204	Epilepsy, nocturnal frontal lobe, 2		HP:0000716	OMIM:603204	TAS					P	HPO:skoehler[2015-12-30]
OMIM:603204	Epilepsy, nocturnal frontal lobe, 2		HP:0000718	OMIM:603204	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:603204	Epilepsy, nocturnal frontal lobe, 2		HP:0000006	OMIM:603204	TAS					I	HPO:skoehler[2013-01-21]
OMIM:140600	Osteoarthritis of distal interphalangeal joints		HP:0002758	OMIM:140600	TAS					P	HPO:probinson[2009-02-17]
OMIM:140600	Osteoarthritis of distal interphalangeal joints		HP:0012313	OMIM:140600	TAS					P	HPO:probinson[2013-08-10]
OMIM:140600	Osteoarthritis of distal interphalangeal joints		HP:0000006	OMIM:140600	TAS					I	HPO:probinson[2013-04-01]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000341	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000582	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0003577	PMID:26633546	PCS		3/3			C	HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000122	PMID:26633546	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000062	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001250	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001274	PMID:26633546	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001290	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0002280	PMID:26633546	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001629	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000316	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001845	PMID:26633546	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000218	OMIM:618142	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001643	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0004736	PMID:26633546	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000278	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0002553	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000252	PMID:26633546	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000054	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0002079	PMID:26633546	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0010751	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0005280	OMIM:618142	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0010954	PMID:26633546	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0010557	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0100259	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0100258	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001339	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000007	PMID:26633546	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001511	PMID:26633546	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000400	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001631	OMIM:618142	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000248	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000369	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0000347	PMID:26633546	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618142	Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome		HP:0001776	PMID:26633546	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:617271	Nephronophthisis 20		HP:0003774	PMID:28089251	PCS		5/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0003676	PMID:28089251	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0000076	PMID:28089251	PCS		1/8			P	HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0003621	PMID:28089251	PCS					C	HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0002650	PMID:28089251	PCS		3/8			P	HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0000083	PMID:28089251	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0011462	PMID:28089251	PCS					C	HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0000107	PMID:28089251	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0000007	PMID:28089251	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617271	Nephronophthisis 20		HP:0000090	PMID:28089251	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0030205	PMID:22742743	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0002650	PMID:22742743	TAS		2/5			P	HPO:skoehler[2012-12-02];HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0003473	PMID:22742743	PCS					P	HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0001252	PMID:22742743	TAS					P	HPO:skoehler[2014-11-26];HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0003593	PMID:22742743	PCS		2/5			C	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0001270	OMIM:614750	TAS					P	HPO:skoehler[2012-12-02]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0100301	PMID:22742743	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0011463	PMID:22742743	PCS		3/5			C	HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0000508	PMID:22742743	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0000007	PMID:22742743	TAS					I	HPO:skoehler[2013-01-11];HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0003701	PMID:22742743	PCS		5/5			P	HPO:skoehler[2012-12-02];HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0003677	OMIM:614750	TAS					C	HPO:skoehler[2012-12-02];HPO:probinson[2020-07-19]
OMIM:614750	Myasthenic syndrome, congenital, 13, with tubular aggregates		HP:0003403	PMID:22742743	PCS					P	HPO:probinson[2020-07-19]
OMIM:145750	Hypertriglyceridemia, familial		HP:0002155	OMIM:145750	IEA					P	HPO:iea[2009-02-17]
OMIM:145750	Hypertriglyceridemia, familial		HP:0003362	OMIM:145750	IEA					P	HPO:iea[2009-02-17]
OMIM:145750	Hypertriglyceridemia, familial		HP:0040075	OMIM:145750	IEA					P	HPO:skoehler[2018-10-08]
OMIM:145750	Hypertriglyceridemia, familial		HP:0004416	OMIM:145750	IEA					P	HPO:iea[2009-02-17]
OMIM:145750	Hypertriglyceridemia, familial		HP:0000006	OMIM:145750	IEA					I	HPO:iea[2009-02-17]
OMIM:145750	Hypertriglyceridemia, familial		HP:0001039	OMIM:145750	IEA					P	HPO:iea[2009-02-17]
OMIM:145750	Hypertriglyceridemia, familial		HP:0001952	OMIM:145750	IEA					P	HPO:iea[2009-02-17]
OMIM:619274	Deafness, autosomal dominant 80		HP:0003577	PMID:29955957	PCS		2/2			C	HPO:probinson[2021-05-29]
OMIM:619274	Deafness, autosomal dominant 80		HP:0011380	PMID:29955957	PCS		2/2			P	HPO:probinson[2021-05-29]
OMIM:619274	Deafness, autosomal dominant 80		HP:0011375	PMID:29955957	PCS		2/2			P	HPO:probinson[2021-05-29]
OMIM:619274	Deafness, autosomal dominant 80		HP:0011379	PMID:29955957	PCS		2/2			P	HPO:probinson[2021-05-29]
OMIM:619274	Deafness, autosomal dominant 80		HP:0000006	PMID:29955957	PCS					I	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619274	Deafness, autosomal dominant 80		HP:0008527	PMID:29955957	PCS		2/2			P	HPO:probinson[2021-05-29]
OMIM:619274	Deafness, autosomal dominant 80		HP:6000988	OMIM:619274	TAS					P	HPO:probinson[2024-08-04]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0002497	OMIM:108650	IEA					P	HPO:iea[2009-02-17]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0003487	OMIM:108650	IEA					P	HPO:iea[2009-02-17]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0007728	OMIM:108650	IEA					P	HPO:iea[2009-02-17]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0000639	OMIM:108650	IEA					P	HPO:iea[2009-02-17]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0001260	OMIM:108650	IEA					P	HPO:iea[2009-02-17]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0002075	OMIM:108650	TAS					P	HPO:skoehler[2012-12-03]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0000549	OMIM:108650	IEA					P	HPO:iea[2009-02-17]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0000648	OMIM:108650	TAS		HP:0040283			P	HPO:skoehler[2012-12-03]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0000006	OMIM:108650	IEA					I	HPO:iea[2009-02-17]
OMIM:108650	Spastic ataxia 7, autosomal dominant		HP:0001347	OMIM:108650	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0001177	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000286	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000582	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000384	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000243	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0004322	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0002002	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000463	OMIM:610536	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0001250	OMIM:610536	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0003196	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0001629	OMIM:610536	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0008551	OMIM:610536	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0008872	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0009623	OMIM:610536	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000413	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000253	OMIM:610536	TAS					P	HPO:skoehler[2015-12-30]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000396	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000252	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000494	OMIM:610536	TAS					P	HPO:skoehler[2012-11-20]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000175	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000750	OMIM:610536	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000453	OMIM:610536	TAS					P	HPO:skoehler[2012-11-21]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0002098	OMIM:610536	TAS					P	HPO:skoehler[2012-11-21]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0002032	OMIM:610536	TAS		HP:0040283			P	HPO:skoehler[2013-02-25]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0005321	OMIM:610536	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0001263	OMIM:610536	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000272	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0011800	OMIM:610536	TAS					P	HPO:skoehler[2013-11-28]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000506	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000405	OMIM:610536	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0001631	OMIM:610536	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0001238	OMIM:610536	TAS					P	HPO:skoehler[2012-11-21]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000347	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000369	OMIM:610536	IEA					P	HPO:iea[2009-02-17]
OMIM:610536	Mandibulofacial dysostosis, Guion-Almeida type		HP:0000006	OMIM:610536	TAS					I	HPO:skoehler[2012-10-17]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0002188	PMID:34494102	PCS		1/1			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0010109	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0002066	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0001252	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0003593	PMID:34494102	PCS		2/2			C	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0002080	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0100703	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0001629	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000319	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0100807	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000876	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000219	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000455	PMID:34494102	PCS		2/2			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0001763	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0002311	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0002136	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000431	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0011968	PMID:34494102	PCS		2/2			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000490	PMID:34494102	PCS		2/2			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0001263	PMID:34494102	PCS		2/2			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000007	PMID:34494102	PCS					I	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0000964	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0004209	PMID:34494102	PCS		1/2			P	HPO:probinson[2023-07-15]
OMIM:620393	Intellectual developmental disorder, autosomal recessive 79		HP:0001238	PMID:34494102	PCS		2/2			P	HPO:probinson[2023-07-15];HPO:probinson[2023-07-15]
OMIM:301800	Anus, imperforate		HP:0000365	OMIM:301800	IEA					P	HPO:iea[2009-02-17]
OMIM:301800	Anus, imperforate		HP:0002023	OMIM:301800	IEA					P	HPO:iea[2009-02-17]
OMIM:301800	Anus, imperforate		HP:0004397	OMIM:301800	IEA					P	HPO:iea[2009-02-17]
OMIM:301800	Anus, imperforate		HP:0001417	OMIM:301800	IEA					I	HPO:iea[2009-02-17]
OMIM:301800	Anus, imperforate		HP:0000047	OMIM:301800	IEA					P	HPO:iea[2009-02-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0003202	OMIM:610250	TAS					P	HPO:probinson[2012-04-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0003621	PMID:16826527	PCS		2/6			C	HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0002015	OMIM:610250	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0003596	PMID:16826527	PCS		1/6			C	HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0000012	OMIM:610250	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0001761	OMIM:610250	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0003487	PMID:16826527	PCS		6/6			P	HPO:probinson[2012-04-17];HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0003693	PMID:16826527	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0001260	OMIM:610250	TAS					P	HPO:probinson[2012-04-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0002064	PMID:16826527	PCS		6/6			P	HPO:probinson[2012-04-17];HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0002061	OMIM:610250	TAS					P	HPO:probinson[2012-04-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0011448	PMID:16826527	PCS		3/6			P	HPO:probinson[2012-04-17];HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0007340	PMID:16826527	PCS		6/6			P	HPO:probinson[2012-04-17];HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0011463	PMID:16826527	PCS		2/6			C	HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0011462	PMID:16826527	PCS		1/6			C	HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0002936	PMID:16826527	PCS		1/6			P	HPO:probinson[2012-04-17];HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0001258	OMIM:610250	TAS					P	HPO:probinson[2012-04-17]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0000006	PMID:16826527	PCS					I	HPO:probinson[2012-04-17];HPO:probinson[2022-09-04]
OMIM:610250	Spastic paraplegia 31, autosomal dominant		HP:0001347	OMIM:610250	TAS					P	HPO:probinson[2012-04-17]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0002069	PMID:34186028	PCS	HP:0011463	2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000286	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001374	PMID:34186028	PCS	HP:0003577	1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0002188	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000486	PMID:34186028	PCS		5/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0002263	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000160	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001252	PMID:34186028	PCS		7/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0032794	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0011933	PMID:34186028	PCS		1/10			P	HPO:probinson[2021-10-30]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0033725	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0012110	PMID:34186028	PCS		3/9			P	HPO:probinson[2021-10-30]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000639	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0011220	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000316	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000239	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000238	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0100807	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000752	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001488	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001249	PMID:34186028	PCS		7/7			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000358	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000556	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000494	PMID:34186028	PCS		3/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000252	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001344	PMID:34186028	PCS		3/8			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000574	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0011968	PMID:34186028	PCS		8/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000293	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001263	PMID:34186028	PCS		8/8			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000294	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0002194	PMID:34186028	PCS		8/8			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0011800	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0003083	PMID:34186028	PCS	HP:0003577	1/11			P	HPO:probinson[2021-10-30]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0009890	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000407	PMID:34186028	PCS		1/8			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000729	PMID:34186028	PCS		3/7			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000601	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000722	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001338	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000648	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0007874	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0004209	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000565	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000400	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0008447	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000322	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000006	PMID:34186028	PCS					I	HPO:probinson[2021-10-30];HPO:probinson[2021-10-30]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000248	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000369	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001776	PMID:34186028	PCS		1/11			P	HPO:probinson[2021-10-30]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000343	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0010945	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000540	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001274	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0010862	PMID:34186028	PCS		8/8			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0012803	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0025161	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001508	PMID:34186028	PCS		4/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000418	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000739	PMID:34186028	PCS		3/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000414	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000733	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000218	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0009765	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-31];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000256	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0002410	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000750	PMID:34186028	PCS		8/8			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001321	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000276	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0005487	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0100321	PMID:34186028	PCS		3/9			P	HPO:probinson[2021-10-30]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0012520	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0032792	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0002804	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0100716	PMID:34186028	PCS		3/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0002007	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001357	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000664	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0001631	PMID:34186028	PCS	HP:0003577	1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000028	PMID:34186028	PCS		1/3	MALE		P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000303	PMID:34186028	PCS		1/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:619512	Neurodevelopmental disorder with hypotonia and brain abnormalities		HP:0000347	PMID:34186028	PCS		2/9			P	HPO:probinson[2021-10-30];HPO:probinson[2021-10-31]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0002751	OMIM:260540	IEA					P	HPO:iea[2009-02-17]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0001300	OMIM:260540	IEA					P	HPO:iea[2009-02-17]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0000726	OMIM:260540	IEA					P	HPO:iea[2009-02-17]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0002063	OMIM:260540	IEA					P	HPO:iea[2009-02-17]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0003581	OMIM:260540	IEA					C	HPO:iea[2009-02-17]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0011462	OMIM:260540	TAS					C	HPO:probinson[2020-11-26]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0002062	OMIM:260540	IEA					P	HPO:iea[2009-02-17]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0007256	OMIM:260540	TAS					P	HPO:skoehler[2014-11-26]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0000007	OMIM:260540	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0000597	OMIM:260540	IEA					P	HPO:iea[2009-02-17]
OMIM:260540	Supranuclear palsy, progressive atypical		HP:0001337	OMIM:260540	IEA					P	HPO:iea[2009-02-17]
OMIM:613981	Hypotrichosis 3		HP:0000164	PMID:21188418	PCS		0/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-01]
OMIM:613981	Hypotrichosis 3		HP:0001597	PMID:21188418	PCS		0/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-01]
OMIM:613981	Hypotrichosis 3		HP:0011463	PMID:21188418	PCS		14/14			C	HPO:probinson[2022-07-01]
OMIM:613981	Hypotrichosis 3		HP:0002209	PMID:21188418	PCS		14/14			P	HPO:probinson[2013-08-10];HPO:probinson[2022-07-01]
OMIM:613981	Hypotrichosis 3		HP:0000499	PMID:21188418	PCS		0/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-01]
OMIM:613981	Hypotrichosis 3		HP:0000971	PMID:21188418	PCS		0/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-01]
OMIM:613981	Hypotrichosis 3		HP:0000006	PMID:21188418	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-07-01]
OMIM:615328	Shaheen syndrome		HP:0000252	OMIM:615328	TAS		HP:0040283			P	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0000670	OMIM:615328	TAS					P	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0003577	OMIM:615328	TAS					C	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0000750	OMIM:615328	TAS					P	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0006297	OMIM:615328	TAS					P	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0000007	OMIM:615328	TAS					I	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0000966	OMIM:615328	TAS					P	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0000972	OMIM:615328	TAS					P	HPO:skoehler[2013-09-10]
OMIM:615328	Shaheen syndrome		HP:0001249	OMIM:615328	TAS					P	HPO:skoehler[2013-09-10]
OMIM:251945	Mitochondrial myopathy with A defect in mitochondrial-protein transport		HP:0001939	OMIM:251945	IEA					P	HPO:iea[2009-02-17]
OMIM:251945	Mitochondrial myopathy with A defect in mitochondrial-protein transport		HP:0000007	OMIM:251945	IEA					I	HPO:iea[2009-02-17]
OMIM:251945	Mitochondrial myopathy with A defect in mitochondrial-protein transport		HP:0003737	OMIM:251945	IEA					P	HPO:skoehler[2015-01-27]
OMIM:251945	Mitochondrial myopathy with A defect in mitochondrial-protein transport		HP:0001324	OMIM:251945	IEA					P	HPO:iea[2009-02-17]
OMIM:251945	Mitochondrial myopathy with A defect in mitochondrial-protein transport		HP:0003546	OMIM:251945	IEA					P	HPO:iea[2009-02-17]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0000054	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0000252	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0003038	OMIM:612447	TAS					P	HPO:probinson[2013-12-15]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0000233	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0000486	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0002750	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0004322	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0003022	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0000160	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0003097	OMIM:612447	TAS					P	HPO:probinson[2013-12-15]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0000007	OMIM:612447	TAS					I	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0009777	OMIM:612447	TAS					P	HPO:skoehler[2010-06-20]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0005815	OMIM:612447	TAS					P	HPO:probinson[2013-12-15]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0006501	OMIM:612447	TAS					P	HPO:probinson[2012-06-03]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0005736	OMIM:612447	TAS					P	HPO:probinson[2013-12-15]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0000028	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612447	Skeletal defects, genital hypoplasia, and impaired intellectual development		HP:0001249	OMIM:612447	TAS					P	HPO:skoehler[2010-06-19]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0001298	PMID:21109225	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-10]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0002059	PMID:21109225	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-10]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0001250	PMID:21109225	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-10]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0011669	PMID:21109225	PCS	HP:0003577	1/4			P	HPO:probinson[2020-10-07]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0012852	PMID:21109225	PCS		1/4			P	HPO:probinson[2020-10-10]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0031964	PMID:21109225	PCS		2/2			P	HPO:probinson[2020-11-06]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0033196	PMID:21109225	PCS		1/4			P	HPO:probinson[2020-10-12];HPO:probinson[2020-10-12];HPO:probinson[2020-11-06]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0001629	PMID:21109225	PCS	HP:0003577	1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0002719	PMID:21109225	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-10]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0003819	PMID:21109225	PCS		2/4			C	HPO:probinson[2020-10-10];HPO:probinson[2020-10-10]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0032550	PMID:21109225	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-10-07]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0033199	PMID:21109225	PCS		1/1			P	HPO:probinson[2020-10-12]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0000007	PMID:21109225	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:613759	Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations		HP:0004935	PMID:21109225	PCS	HP:0003577	1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:188050	Thrombophiliavenous thromboembolism, included		HP:0001907	OMIM:188050	IEA					P	HPO:skoehler[2015-01-27]
OMIM:188050	Thrombophiliavenous thromboembolism, included		HP:0011463	OMIM:188050	TAS					C	HPO:probinson[2012-07-21]
OMIM:188050	Thrombophiliavenous thromboembolism, included		HP:0004419	OMIM:188050	TAS					P	HPO:probinson[2009-02-17]
OMIM:188050	Thrombophiliavenous thromboembolism, included		HP:0002625	OMIM:188050	TAS					P	HPO:probinson[2012-07-21]
OMIM:188050	Thrombophiliavenous thromboembolism, included		HP:0000006	OMIM:188050	TAS					I	HPO:probinson[2009-02-17]
OMIM:188050	Thrombophiliavenous thromboembolism, included		HP:0002204	OMIM:188050	TAS					P	HPO:probinson[2012-07-21]
OMIM:188050	Thrombophiliavenous thromboembolism, included		HP:0005305	OMIM:188050	TAS					P	HPO:probinson[2012-07-21]
OMIM:173590	Platelet signal processing defect		HP:0001892	OMIM:173590	TAS					P	HPO:probinson[2009-02-17]
OMIM:173590	Platelet signal processing defect		HP:0008320	OMIM:173590	TAS					P	HPO:probinson[2012-09-10]
OMIM:173590	Platelet signal processing defect		HP:0008148	OMIM:173590	TAS					P	HPO:probinson[2012-09-10]
OMIM:173590	Platelet signal processing defect		HP:0000421	OMIM:173590	TAS					P	HPO:probinson[2009-02-17]
OMIM:173590	Platelet signal processing defect		HP:0001873	OMIM:173590	TAS					P	HPO:probinson[2009-02-17]
OMIM:173590	Platelet signal processing defect		HP:0000006	OMIM:173590	TAS					I	HPO:probinson[2009-02-17]
OMIM:173590	Platelet signal processing defect		HP:0004866	OMIM:173590	TAS					P	HPO:probinson[2012-09-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0004754	PMID:18088563	PCS		1/2			P	HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0001297	PMID:18088563	PCS		3/6			P	HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0003596	PMID:18088563	PCS		2/2			C	HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0001662	PMID:18088563	PCS		5/6			P	HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0031295	PMID:18088563	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0005133	PMID:18088563	PCS		3/6			P	HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0001712	PMID:18088563	PCS		1/6			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0004749	PMID:18088563	PCS		1/5			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0004757	PMID:18088563	PCS		1/2			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0000006	PMID:18088563	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-10]
OMIM:614022	Atrial fibrillation, familial, 10		HP:0005180	PMID:18088563	PCS		2/2			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-10]
OMIM:600057	Exstrophy of bladder		HP:0000023	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0000122	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0000072	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0000085	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0002836	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0000006	OMIM:600057	IEA					I	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0000039	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0030911	OMIM:600057	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600057	Exstrophy of bladder		HP:0001545	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:600057	Exstrophy of bladder		HP:0002644	OMIM:600057	IEA					P	HPO:iea[2009-02-17]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0002663	PMID:30804514	PCS		3/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0005348	PMID:30804514	PCS		2/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0001156	PMID:30804514	PCS		3/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0003165	PMID:30804514	PCS		0/3			P	HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0003196	PMID:30804514	PCS		3/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0011800	PMID:30804514	PCS		3/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0010230	PMID:30804514	PCS		3/3			P	HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0002905	PMID:30804514	PCS		0/3			P	HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0008873	PMID:30804514	PCS		3/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0000505	PMID:30804514	PCS		0/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0002901	PMID:30804514	PCS		0/3			P	HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0002205	PMID:30804514	PCS		2/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0200055	PMID:30804514	PCS		3/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0000006	PMID:30804514	PCS					I	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618618	Spondyloepiphyseal dysplasia, Nishimura type		HP:0001249	PMID:30804514	IEA		0/3			P	HPO:probinson[2020-07-22];HPO:probinson[2024-03-16]
OMIM:272150	Sugarman brachydactyly		HP:0001156	OMIM:272150	TAS					P	HPO:skoehler[2014-11-26]
OMIM:272150	Sugarman brachydactyly		HP:0005894	OMIM:272150	IEA					P	HPO:iea[2009-02-17]
OMIM:272150	Sugarman brachydactyly		HP:0010241	OMIM:272150	TAS					P	HPO:probinson[2012-06-09]
OMIM:272150	Sugarman brachydactyly		HP:0011926	OMIM:272150	TAS					P	HPO:probinson[2012-06-09]
OMIM:272150	Sugarman brachydactyly		HP:0000007	OMIM:272150	IEA					I	HPO:iea[2009-02-17]
OMIM:272150	Sugarman brachydactyly		HP:0009857	OMIM:272150	TAS					P	HPO:probinson[2012-06-09]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0001762	OMIM:610244	TAS					P	HPO:probinson[2012-04-17]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0003487	OMIM:610244	TAS					P	HPO:probinson[2012-04-17]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0007340	OMIM:610244	TAS					P	HPO:probinson[2012-04-17]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0002064	OMIM:610244	TAS	HP:0003581				P	HPO:probinson[2012-04-17]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0002061	OMIM:610244	TAS					P	HPO:probinson[2012-04-17]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0001258	OMIM:610244	IEA					P	HPO:skoehler[2015-01-27]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0000006	OMIM:610244	TAS					I	HPO:probinson[2012-04-17]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0011448	OMIM:610244	TAS					P	HPO:probinson[2012-04-17]
OMIM:610244	Spastic paraplegia 33, autosomal dominant		HP:0001347	OMIM:610244	TAS					P	HPO:probinson[2012-04-17]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0001386	PMID:39414788	PCS		12/14			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0003301	PMID:39414788	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0006429	PMID:39414788	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0002650	PMID:39414788	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0004576	PMID:39414788	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0001376	PMID:39414788	PCS		9/11			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0001387	PMID:39414788	PCS		1/11			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0004586	PMID:39414788	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0002970	PMID:39414788	PCS		3/13			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0004322	PMID:39414788	PCS		8/14			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0004474	PMID:39414788	PCS		2/13			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0100864	PMID:39414788	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0100774	PMID:39414788	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0002829	PMID:39414788	PCS		12/14			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0002808	PMID:39414788	PCS		2/13			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0011463	PMID:39414788	PCS		1/5			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0100734	PMID:39414788	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0011462	PMID:39414788	PCS		4/5			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0000926	PMID:39414788	PCS		7/9			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0002515	PMID:39414788	PCS		14/14			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0002857	PMID:39414788	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0002868	PMID:39414788	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0004349	PMID:39414788	PCS		6/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621099	Spondyloepimetaphyseal dysplasia, Li-Shao-Li type		HP:0000006	PMID:39414788	PCS					I	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000252	OMIM:601349	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000175	OMIM:601349	TAS					P	HPO:probinson[2012-07-16]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000482	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000581	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0012745	OMIM:601349	TAS					P	HPO:skoehler[2014-03-24]
OMIM:601349	Microphthalmia, syndromic 8		HP:0100678	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0001839	OMIM:601349	TAS					P	HPO:probinson[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000568	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000202	OMIM:601349	IEA					P	HPO:skoehler[2010-06-18]
OMIM:601349	Microphthalmia, syndromic 8		HP:0001566	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000028	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000204	OMIM:601349	TAS					P	HPO:probinson[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000303	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0001249	OMIM:601349	IEA					P	HPO:iea[2009-02-17]
OMIM:601349	Microphthalmia, syndromic 8		HP:0000006	OMIM:601349	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0003510	OMIM:308830	PCS					P	HPO:probinson[2009-02-17]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0007439	OMIM:308830	PCS					P	HPO:probinson[2009-02-17]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0002223	OMIM:308830	PCS					P	HPO:probinson[2012-02-21]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0000561	OMIM:308830	PCS					P	HPO:probinson[2012-02-21]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0000252	OMIM:308830	PCS					P	HPO:probinson[2009-02-17]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0002059	OMIM:308830	PCS					P	HPO:probinson[2009-02-17]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0002298	OMIM:308830	PCS					P	HPO:probinson[2009-02-17]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0003819	OMIM:308830	PCS					C	HPO:probinson[2009-02-17]
OMIM:308830	Keratosis follicularis, dwarfism, and cerebral atrophy		HP:0001417	OMIM:308830	PCS					I	HPO:probinson[2009-02-17]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002188	PMID:32533184	PCS		3/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0004586	PMID:32533184	PCS		2/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0004322	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0001272	PMID:33668384;PMID:32533184	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0001252	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0031609	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0001251	PMID:33668384;PMID:32533184	PCS		3/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0003593	PMID:32533184	PCS		3/3			C	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000280	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0012444	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0012765	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000518	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000639	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0040079	PMID:32533184	PCS		2/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0008499	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0003429	PMID:33668384;PMID:32533184	PCS		3/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002318	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0007401	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0007843	PMID:33668384;PMID:32533184	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000577	PMID:32533184	PCS		2/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002655	PMID:33668384;PMID:32533184	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000550	PMID:33668384;PMID:32533184	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000154	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0005667	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0008936	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002059	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002650	PMID:32533184	PCS		2/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0006958	PMID:32533184	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0031936	PMID:32533184	PCS		3/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002750	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002079	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002352	PMID:33668384;PMID:32533184	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0001263	PMID:33668384;PMID:32533184	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0002273	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0011003	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0005280	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0100660	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000407	PMID:33668384;PMID:32533184	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0010582	PMID:32533184	PCS		3/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000007	PMID:32533184	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000546	PMID:33668384	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000505	PMID:32533184	PCS		3/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000543	PMID:33668384;PMID:32533184	PCS		2/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0000664	PMID:32533184	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0001510	PMID:33668384;PMID:32533184	PCS		4/4			P	HPO:probinson[2021-06-20]
OMIM:619260	Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis		HP:0001116	PMID:33668384;PMID:32533184	PCS		3/4			P	HPO:probinson[2021-06-20]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000286	PMID:22770981	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0005216	PMID:22770981	PCS		2/2			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0003577	PMID:22770981;PMID:26007620	PCS		3/3			C	HPO:probinson[2022-10-22];HPO:skoehler[2019-02-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0010628	PMID:22770981;PMID:26007620	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0010804	PMID:26007620	PCS		1/1			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000463	PMID:22770981;PMID:26007620	PCS		3/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0003196	PMID:26007620	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000319	PMID:22770981	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000337	PMID:22770981	PCS		1/2			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0002714	PMID:26007620	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000218	PMID:26007620	PCS		1/1			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0007687	PMID:26007620	PCS		1/1			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000358	PMID:22770981	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0002058	OMIM:614744	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0002015	OMIM:614744	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000750	OMIM:614744	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0011968	PMID:22770981	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000194	PMID:22770981	PCS		2/2			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0001260	OMIM:614744	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0025312	OMIM:614744	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0030001	PMID:22770981;PMID:26007620	PCS		3/3			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0003680	PMID:26007620	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0011800	PMID:22770981;PMID:26007620	PCS		3/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0005280	PMID:26007620	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000407	OMIM:614744	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000007	PMID:22770981	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000565	PMID:26007620	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000322	PMID:22770981	PCS		1/2			P	HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000369	PMID:22770981;PMID:26007620	PCS		3/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-22];HPO:probinson[2022-10-22]
OMIM:614744	Facial paresis, hereditary congenital, 3		HP:0000347	PMID:22770981	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-22]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0002166	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0001761	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0003487	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0003693	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0002064	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0002460	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0002061	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0003392	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0003393	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0007340	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0003426	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0001258	OMIM:612335	IEA					P	HPO:skoehler[2015-01-27]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0003427	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0000006	OMIM:612335	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612335	Spastic paraplegia 38, autosomal dominant		HP:0001347	OMIM:612335	IEA					P	HPO:skoehler[2010-06-19]
OMIM:619937	Spermatogenic failure 74		HP:0003251	PMID:34755185	PCS		4/4			P	HPO:probinson[2022-08-04]
OMIM:619937	Spermatogenic failure 74		HP:0011462	PMID:34755185	PCS		4/4			C	HPO:probinson[2022-08-04];HPO:probinson[2022-08-04]
OMIM:619937	Spermatogenic failure 74		HP:0000007	PMID:34755185	PCS					I	HPO:probinson[2022-08-04]
OMIM:619937	Spermatogenic failure 74		HP:0031038	PMID:34755185	PCS		1/1			P	HPO:probinson[2022-08-04]
OMIM:619937	Spermatogenic failure 74		HP:0011961	PMID:34755185	PCS		4/4			P	HPO:probinson[2022-08-04]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0033542	PMID:25657025	PCS					P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0045051	PMID:11991887	PCS					P	HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0033328	PMID:11207353	PCS		1/1			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0001508	PMID:11991887	PCS		1/14			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0032341	PMID:11991887	PCS					P	HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0032980	PMID:11207353	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002878	PMID:11207353	PCS		1/1			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0006532	PMID:25657025	PCS		17/17			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0005942	PMID:25657025;PMID:11207353	PCS		3/11			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0006515	OMIM:610913	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0033638	PMID:25657025	PCS		2/6			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0006517	OMIM:610913	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0025394	PMID:25657025	PCS		6/6			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002098	PMID:11207353	PCS	HP:0003623				P	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002110	PMID:25657025	PCS					P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0001263	PMID:25657025	PCS		2/17			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0025179	PMID:25657025	PCS		6/6			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002094	PMID:11991887	PCS		9/14			P	HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0012735	PMID:11991887	PCS		8/14			P	HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002092	PMID:25657025	PCS		2/17			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0012418	PMID:25657025	PCS		17/17			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002093	PMID:11207353	PCS		1/1			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0033584	PMID:25657025;PMID:11207353	PCS		8/11			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0001217	PMID:11991887	PCS		5/14			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002108	PMID:25657025	PCS		3/17			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0000961	PMID:11991887	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002206	PMID:25657025	PCS		1/17			P	HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0002789	PMID:11991887	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-05]
OMIM:610913	Surfactant metabolism dysfunction, pulmonary, 2		HP:0000006	PMID:11207353	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002521	OMIM:618397	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0003577	PMID:26016410	PCS		2/2			C	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001332	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001371	OMIM:618397	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001272	PMID:26016410	PCS		2/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0012707	PMID:26016410	PCS		1/1			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0012708	PMID:26016410	PCS		1/1			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0100651	PMID:22700954	PCS		2/2			P	HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0000817	PMID:26016410	PCS		2/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002119	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001302	OMIM:618397	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001688	PMID:26016410	PCS		2/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002058	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0000252	PMID:22700954	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002059	PMID:26016410	PCS		1/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002650	PMID:26016410	PCS		1/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0000750	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002376	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0003487	PMID:26016410	PCS		1/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0011968	PMID:26016410	PCS		2/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0011924	PMID:26016410	PCS		2/2			P	HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001260	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002151	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001263	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002490	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0011448	PMID:26016410	PCS		1/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0034392	PMID:26016410	PCS		1/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0003819	PMID:26016410	PCS		1/2			C	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002803	PMID:26016410	PCS		2/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0000007	PMID:22700954	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002804	PMID:26016410	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0008347	PMID:26016410	PCS		2/2			P	HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002307	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0002205	PMID:26016410	PCS		1/2			P	HPO:probinson[2023-02-09];HPO:probinson[2023-02-09]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001511	OMIM:618397	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0001257	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0004305	OMIM:618397	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618397	Combined oxidative phosphorylation deficiency 39		HP:0009879	PMID:22700954	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-09]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0004798	OMIM:608184	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002110	OMIM:608184	TAS					P	HPO:iea[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0001890	OMIM:608184	IEA					P	HPO:iea[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002849	OMIM:608184	IEA					P	HPO:iea[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002959	OMIM:608184	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002718	OMIM:608184	TAS					P	HPO:skoehler[2010-06-20]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0000007	OMIM:608184	IEA					I	HPO:iea[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0001973	OMIM:608184	IEA					P	HPO:iea[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002788	OMIM:608184	IEA					P	HPO:iea[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002863	OMIM:608184	IEA					P	HPO:iea[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002721	OMIM:608184	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608184	Immunodeficiency with hyper-IgM, type 4		HP:0002754	OMIM:608184	IEA					P	HPO:iea[2009-02-17]
OMIM:174770	Actinic prurigo		HP:0000099	OMIM:174770	TAS					P	HPO:skoehler[2013-01-22]
OMIM:174770	Actinic prurigo		HP:0000992	OMIM:174770	TAS					P	HPO:iea[2009-02-17]
OMIM:174770	Actinic prurigo		HP:0100825	OMIM:174770	TAS					P	HPO:skoehler[2013-01-22]
OMIM:174770	Actinic prurigo		HP:0000999	OMIM:174770	TAS					P	HPO:skoehler[2010-06-20]
OMIM:174770	Actinic prurigo		HP:0000006	OMIM:174770	IEA					I	HPO:iea[2009-02-17]
OMIM:215450	Chorea, benign familial		HP:0002072	OMIM:215450	IEA					P	HPO:iea[2009-02-17]
OMIM:215450	Chorea, benign familial		HP:0000007	OMIM:215450	IEA					I	HPO:iea[2009-02-17]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001342	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0033606	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001297	PMID:9883725	PCS		3/11	FEMALE		P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0000486	PMID:9883725	PCS	HP:0003577	2/11			P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0003256	OMIM:300049	IEA					P	HPO:iea[2009-02-17]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0002079	PMID:9883725	PCS		3/11			P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001321	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001250	OMIM:300049	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0002282	OMIM:300049	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0033725	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0009381	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0002719	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001647	PMID:9883725	PCS		1/11	FEMALE		P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0030084	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001423	PMID:9883725	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001643	OMIM:300049	IEA					P	HPO:iea[2009-02-17]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001643	PMID:9883725	PCS		3/11	FEMALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0001159	PMID:9883725	PCS		1/1	MALE		P	HPO:probinson[2022-08-27]
OMIM:300049	Heterotopia, periventricular, X-linked dominant		HP:0002269	OMIM:300049	IEA					P	HPO:iea[2009-02-17]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0000297	OMIM:618383	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0000252	PMID:29893856	PCS		5/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0000750	PMID:29893856	PCS		9/9			P	HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0001321	PMID:29893856	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0031936	PMID:29893856	PCS		2/3			P	HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0001260	OMIM:618383	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0001263	PMID:29893856	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0001252	PMID:29893856	PCS		1/4			P	HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0001251	PMID:29893856	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0000007	PMID:29893856	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0430028	OMIM:618383	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0002119	PMID:29893856	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0002307	PMID:29893856	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:618383	Intellectual developmental disorder, autosomal recessive 69		HP:0001257	PMID:29893856	PCS		3/3			P	HPO:probinson[2022-12-14]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0000121	PMID:34607910	PCS		6/9			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0003621	PMID:34607910	PCS		3/9			C	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0001250	PMID:34607910	PCS		2/8			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0003593	PMID:34607910	PCS		2/9			C	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0001281	PMID:34607910	PCS		3/8			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0012664	PMID:34607910	PCS		5/6			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0034307	PMID:34607910	PCS		5/6			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0025708	PMID:34607910	PCS		1/9			C	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0002917	PMID:34607910	PCS		9/9			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0011463	PMID:34607910	PCS		3/9			C	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0002902	PMID:34607910	PCS		4/9			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0002900	PMID:34607910	PCS		4/9			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0002901	PMID:34607910	PCS		4/9			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0000103	PMID:34607910	PCS		5/9			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0000006	PMID:34607910	PCS					I	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0001942	PMID:34607910	PCS		4/8			P	HPO:probinson[2023-04-09]
OMIM:620152	Hypomagnesemia 7, renal, with or without dilated cardiomyopathy		HP:0001644	PMID:34607910	PCS		6/9			P	HPO:probinson[2023-04-09]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0030953	OMIM:167730	TAS					P	HPO:skoehler[2017-07-13]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0009926	PMID:23636874	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0003577	PMID:23636874	PCS		1/1			C	HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0010748	PMID:23636874	PCS		1/1			P	HPO:probinson[2012-04-07];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000431	PMID:23636874	PCS		1/1			P	HPO:probinson[2012-04-07];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0001092	PMID:23636874	PCS		1/1			P	HPO:probinson[2012-04-07];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0010566	PMID:23636874	PCS		1/1			P	HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0005280	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0045075	PMID:23636874	PCS		1/1			P	HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0040164	PMID:23636874	PCS		1/1			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000506	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000316	OMIM:167730	PCS					P	HPO:probinson[2012-04-07]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000327	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000349	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000337	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000568	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0004209	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000636	PMID:23636874	PCS		1/1			P	HPO:probinson[2012-04-07];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000378	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000268	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000652	PMID:23636874	PCS		1/1			P	HPO:probinson[2012-04-07];HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000006	OMIM:167730	PCS					I	HPO:probinson[2012-04-07]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000589	PMID:23636874	PCS		1/1			P	HPO:probinson[2022-09-11]
OMIM:167730	Nasopalpebral lipoma-coloboma syndrome		HP:0000369	PMID:23636874	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-11]
OMIM:300707	STAR syndrome		HP:0000066	PMID:18297069	PCS		4/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000143	PMID:18297069;PMID:28225384	PCS		2/7			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07];HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0003577	PMID:18297069;PMID:28225384	PCS		7/7			C	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001770	PMID:18297069	PCS		6/6			P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0002023	PMID:18297069;PMID:28225384	PCS		7/7			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0004322	PMID:18297069	PCS		4/6			P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0003298	PMID:28225384	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000460	OMIM:300707	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300707	STAR syndrome		HP:0001153	PMID:18297069	PCS		2/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001647	PMID:18297069	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000954	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000337	OMIM:300707	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300707	STAR syndrome		HP:0000813	PMID:18297069;PMID:28225384	PCS		3/7			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07];HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000219	OMIM:300707	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300707	STAR syndrome		HP:0000455	OMIM:300707	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300707	STAR syndrome		HP:0004736	PMID:18297069	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001423	PMID:18297069	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0009921	PMID:28225384	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0010716	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001363	PMID:18297069	PCS		2/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000076	PMID:18297069	PCS		4/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001382	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000072	PMID:18297069	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0005343	PMID:18297069	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000394	PMID:18297069	PCS		4/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0004692	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0011003	PMID:18297069	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0005280	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0034350	PMID:18297069	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001518	PMID:18297069	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000506	PMID:18297069;PMID:28225384	PCS		5/7			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07];HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0004969	PMID:18297069	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0004209	PMID:18297069	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0008665	PMID:18297069;PMID:28225384	PCS		3/7			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07];HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0009779	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001511	PMID:18297069	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000125	PMID:18297069	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001631	PMID:18297069	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000369	PMID:18297069	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001776	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000126	PMID:18297069	PCS		2/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0001655	PMID:18297069	PCS		1/6			P	HPO:probinson[2023-02-07]
OMIM:300707	STAR syndrome		HP:0000445	PMID:28225384	PCS		1/1			P	HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0003200	OMIM:545000	TAS					P	HPO:probinson[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0002123	OMIM:545000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0003542	OMIM:545000	TAS					P	HPO:probinson[2013-03-30]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0001250	OMIM:545000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0003198	OMIM:545000	IEA					P	HPO:iea[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0000407	OMIM:545000	IEA					P	HPO:iea[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0002151	OMIM:545000	TAS					P	HPO:probinson[2013-03-30]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0001251	OMIM:545000	IEA					P	HPO:iea[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0001427	OMIM:545000	IEA					I	HPO:iea[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0001324	OMIM:545000	IEA					P	HPO:iea[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0001257	OMIM:545000	IEA					P	HPO:iea[2009-02-17]
OMIM:545000	Myoclonic epilepsy associated with ragged-red fibers		HP:0001336	OMIM:545000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0004325	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000054	PMID:27158779	PCS	HP:0003577	1/1	MALE		P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000365	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000750	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000089	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0004322	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000161	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0005487	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000470	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0003186	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0010442	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0100759	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0009577	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000448	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0001636	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000007	PMID:27158779	PCS					I	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0006145	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0002705	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0002119	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0003429	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0030084	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0009944	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000278	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:617926	Orofaciodigital syndrome XVII		HP:0000369	PMID:27158779	PCS	HP:0003577	1/1			P	HP:probinson[2018-07-04]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0003577	OMIM:259100	IEA					C	HPO:skoehler[2010-06-19]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0001376	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0002684	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0001051	OMIM:259100	TAS					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000280	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0010783	OMIM:259100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000939	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000938	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000239	OMIM:259100	IEA					P	HPO:iea[2009-02-17]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000975	OMIM:259100	TAS					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000218	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000972	OMIM:259100	TAS					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0001643	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0001369	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000890	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0001582	OMIM:259100	TAS					P	HPO:skoehler[2012-08-01]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0003040	OMIM:259100	IEA					P	HPO:skoehler[2015-01-27]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0001519	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0002829	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0009771	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0031284	OMIM:259100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000508	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000767	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000007	OMIM:259100	IEA					I	HPO:iea[2009-02-17]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0000964	OMIM:259100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0001217	OMIM:259100	IEA					P	HPO:iea[2009-02-17]
OMIM:259100	Hypertrophic osteoarthropathy, primary, autosomal recessive 1		HP:0002645	OMIM:259100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:210500	Biliary atresia, extrahepatic		HP:0003676	OMIM:210500	TAS					C	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0003573	OMIM:210500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0005242	OMIM:210500	TAS					P	HPO:probinson[2009-02-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0002240	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0001394	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0003593	OMIM:210500	TAS					C	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0010982	OMIM:210500	TAS					I	HPO:probinson[2024-08-03]
OMIM:210500	Biliary atresia, extrahepatic		HP:0011984	OMIM:210500	TAS					P	HPO:probinson[2012-07-19]
OMIM:210500	Biliary atresia, extrahepatic		HP:0011985	OMIM:210500	TAS					P	HPO:probinson[2012-07-19]
OMIM:210500	Biliary atresia, extrahepatic		HP:0008282	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0006580	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0001408	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0002904	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0002910	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:210500	Biliary atresia, extrahepatic		HP:0000952	OMIM:210500	TAS					P	HPO:probinson[2012-07-17]
OMIM:242520	Ichthyosis, hepatosplenomegaly, and cerebellar degeneration		HP:0008064	OMIM:242520	IEA					P	HPO:iea[2009-02-17]
OMIM:242520	Ichthyosis, hepatosplenomegaly, and cerebellar degeneration		HP:0001260	OMIM:242520	IEA					P	HPO:iea[2009-02-17]
OMIM:242520	Ichthyosis, hepatosplenomegaly, and cerebellar degeneration		HP:0001251	OMIM:242520	IEA					P	HPO:iea[2009-02-17]
OMIM:242520	Ichthyosis, hepatosplenomegaly, and cerebellar degeneration		HP:0000007	OMIM:242520	IEA					I	HPO:iea[2009-02-17]
OMIM:242520	Ichthyosis, hepatosplenomegaly, and cerebellar degeneration		HP:0001433	OMIM:242520	IEA					P	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0000771	OMIM:202110	IEA					P	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0000062	OMIM:202110	IEA					P	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0001949	OMIM:202110	IEA					P	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0008221	OMIM:202110	IEA					P	HPO:skoehler[2015-01-19]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0000822	OMIM:202110	IEA					P	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0000007	OMIM:202110	IEA					I	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0000037	OMIM:202110	IEA					P	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0000840	OMIM:202110	IEA					P	HPO:iea[2009-02-17]
OMIM:202110	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency		HP:0000786	OMIM:202110	IEA					P	HPO:iea[2009-02-17]
OMIM:182970	Spinal muscular atrophy, Facioscapulohumeral type		HP:0003202	OMIM:182970	IEA					P	HPO:skoehler[2010-06-20]
OMIM:182970	Spinal muscular atrophy, Facioscapulohumeral type		HP:0007269	OMIM:182970	IEA					P	HPO:skoehler[2015-01-27]
OMIM:182970	Spinal muscular atrophy, Facioscapulohumeral type		HP:0000006	OMIM:182970	TAS					I	HPO:skoehler[2013-05-29]
OMIM:314000	Thrombocytopenia with elevated serum IgA and renal disease		HP:0000099	OMIM:314000	IEA					P	HPO:iea[2009-02-17]
OMIM:314000	Thrombocytopenia with elevated serum IgA and renal disease		HP:0001892	OMIM:314000	IEA					P	HPO:iea[2009-02-17]
OMIM:314000	Thrombocytopenia with elevated serum IgA and renal disease		HP:0000790	OMIM:314000	IEA					P	HPO:iea[2009-02-17]
OMIM:314000	Thrombocytopenia with elevated serum IgA and renal disease		HP:0003261	OMIM:314000	IEA					P	HPO:iea[2009-02-17]
OMIM:314000	Thrombocytopenia with elevated serum IgA and renal disease		HP:0001417	OMIM:314000	IEA					I	HPO:iea[2009-02-17]
OMIM:314000	Thrombocytopenia with elevated serum IgA and renal disease		HP:0001873	OMIM:314000	IEA					P	HPO:iea[2009-02-17]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0002014	PMID:17709424	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0002850	PMID:17675462;PMID:17709424	PCS		2/2			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0004432	PMID:17709424	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0003593	PMID:17675462;PMID:17709424	PCS		2/2			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0011109	PMID:17709424	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0010976	PMID:17675462;PMID:17709424	PCS		2/2			P	HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0000509	PMID:17709424	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0002718	PMID:17675462	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0000007	PMID:17675462	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0000403	PMID:17709424	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0002837	PMID:17675462;PMID:17709424	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0006532	PMID:17675462	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0002843	PMID:17709424	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0002720	PMID:17675462;PMID:17709424	PCS		2/2			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:612692	Agammaglobulinemia 6, autosomal recessive		HP:0004315	PMID:17675462;PMID:17709424	PCS		2/2			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002069	PMID:15459825	PCS		4/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002301	OMIM:602481	IEA					P	HPO:iea[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002321	OMIM:602481	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001310	PMID:15459825	PCS		1/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002186	OMIM:602481	TAS					P	HPO:probinson[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001272	PMID:15459825	PCS		1/5			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002066	PMID:15459825	PCS		1/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002381	PMID:15459825;OMIM:602481	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02];HPO:iea[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002181	PMID:15459825	PCS		2/6			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0000639	PMID:15459825	PCS		1/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0011462	PMID:15459825	PCS		4/7			C	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0003829	OMIM:602481	IEA					I	HPO:iea[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001945	PMID:15459825	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001269	PMID:15459825	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002018	PMID:15459825	PCS		8/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001125	OMIM:602481	IEA					P	HPO:iea[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001249	PMID:15459825	PCS		0/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0003621	PMID:15459825	PCS		3/7			C	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001289	PMID:15459825	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0000651	OMIM:602481	TAS					P	HPO:probinson[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002131	OMIM:602481	IEA					P	HPO:iea[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002076	PMID:15459825	PCS		8/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001260	OMIM:602481	TAS					P	HPO:probinson[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002077	PMID:15459825	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0011153	PMID:15459825	PCS		1/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0002329	OMIM:602481	IEA					P	HPO:iea[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0000006	PMID:15459825	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0000622	OMIM:602481	TAS					P	HPO:probinson[2009-02-17]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001337	PMID:15459825	PCS		1/8			P	HPO:probinson[2022-09-02]
OMIM:602481	Migraine, familial hemiplegic, 2		HP:0001259	PMID:15459825	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-02]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000343	PMID:10951463	PCS		5/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000486	PMID:19133692	PCS		3/28			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0002167	PMID:20603595	PCS		HP:0040281			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001156	PMID:12404101;PMID:20603595	PCS		3/26			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0100490	PMID:12404101;PMID:20603595	PCS		4/26			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000085	PMID:19133692;PMID:20603595	PCS		4/22			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001548	PMID:19133692;PMID:12404101	PCS		HP:0040282			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000414	PMID:10951463	PCS		3/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0030680	PMID:19133692;PMID:12404101;PMID:20603595;PMID:10951463	PCS		12/44			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000218	PMID:10951463	PCS		3/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000113	PMID:19133692	PCS		1/16			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000377	PMID:12404101	PCS		9/10			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001367	PMID:10951463	PCS		5/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000256	PMID:12404101	PCS		8/10			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001249	PMID:19133692;PMID:12404101	PCS		HP:0040281			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001166	PMID:10951463;PMID:12404101;PMID:20603595	PCS		9/31			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000077	PMID:19133692;PMID:20603595	PCS		10/22			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000076	PMID:19133692	PCS		1/16			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001363	PMID:19133692	PCS		6/28			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000494	PMID:10951463;PMID:12404101	PCS		9/15			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000431	PMID:10951463	PCS		5/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0002650	PMID:19133692;PMID:12404101;PMID:19262081	PCS		6/30			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000276	PMID:19133692;PMID:12404101;PMID:20603595	PCS		HP:0040281			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001167	PMID:10951463;PMID:12404101;PMID:20603595	PCS		21/31			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000293	PMID:20603595	PCS		8/15			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001382	PMID:12404101	PCS		3/10			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001780	PMID:20603595	PCS		3/16			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000470	PMID:12404101	PCS		4/10			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0010511	PMID:10951463	PCS		4/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0005580	PMID:19133692	PCS		1/16			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001182	PMID:12404101;PMID:20603595	PCS		4/26			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0009890	PMID:19133692	PCS		25/26			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000407	PMID:10951463	PCS		3/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0001999	PMID:19133692;PMID:12404101;PMID:20603595	PCS		HP:0040281			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000448	PMID:19133692;PMID:12404101;PMID:20603595	PCS		31/36			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000303	PMID:19133692;PMID:20603595	PCS		26/33			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000347	PMID:10951463	PCS		4/5			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000369	PMID:12404101	PCS		8/10			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000325	PMID:12404101	PCS		8/10			P	HPO:iea[2011-04-03]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000104	PMID:19133692	PCS		1/16			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000126	PMID:19133692	PCS		4/16			P	HPO:iea[2012-04-24]
DECIPHER:81	15q26 overgrowth syndrome		HP:0000324	PMID:10951463;PMID:12404101	PCS		8/15			P	HPO:iea[2012-04-24]
OMIM:310500	Night blindness, congenital stationary, type 1A		HP:0012047	OMIM:310500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:310500	Night blindness, congenital stationary, type 1A		HP:0001419	PMID:16670814	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-20]
OMIM:310500	Night blindness, congenital stationary, type 1A		HP:0011463	PMID:16670814	PCS		5/5			C	HPO:probinson[2023-02-20]
OMIM:310500	Night blindness, congenital stationary, type 1A		HP:0007642	PMID:16670814	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:310500	Night blindness, congenital stationary, type 1A		HP:0011003	PMID:16670814	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0002762	PMID:11739418;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0002982	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0003038	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0001191	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0031095	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0008873	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0000218	PMID:11739418;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0002996	OMIM:127300	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0006459	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0003367	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0003027	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0002650	PMID:11739418;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0003102	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0002673	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0003022	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0003067	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS			FEMALE		P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0010044	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0005916	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0002986	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0003712	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0005736	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0006248	OMIM:127300	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0000006	OMIM:127300	PCS					I	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0002984	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS					P	HPO:iea[2009-02-17]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0001832	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:127300	Leri-Weill dyschondrosteosis		HP:0001831	ISBN-13:978-0721606156	PCS					P	HPO:iea[2010-08-13]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0009827	OMIM:601163	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0001770	OMIM:601163	IEA					P	HPO:iea[2009-02-17]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0002089	OMIM:601163	IEA					P	HPO:iea[2009-02-17]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0000463	OMIM:601163	TAS					P	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0004331	OMIM:601163	IEA					P	HPO:iea[2009-02-17]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0000316	OMIM:601163	TAS				HP:0012825	P	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0000029	OMIM:601163	TAS					P	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0000007	OMIM:601163	TAS					I	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0001539	OMIM:601163	IEA					P	HPO:iea[2009-02-17]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0004209	OMIM:601163	TAS					P	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0001159	OMIM:601163	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0002566	OMIM:601163	TAS					P	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0000776	OMIM:601163	TAS					P	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0000369	OMIM:601163	TAS					P	HPO:skoehler[2013-07-30]
OMIM:601163	Diaphragmatic defects, limb deficiencies, and ossification defects of skull		HP:0000775	OMIM:601163	IEA					P	HPO:iea[2009-02-17]
OMIM:618432	Hydatidiform mole, recurrent, 4		HP:0032192	PMID:30388401	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618432	Hydatidiform mole, recurrent, 4		HP:0008222	PMID:30388401	PCS		2/2			P	HPO:probinson[2020-07-14]
OMIM:618432	Hydatidiform mole, recurrent, 4		HP:0000007	PMID:30388401	PCS					I	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618432	Hydatidiform mole, recurrent, 4		HP:0200067	PMID:30388401	PCS					H	HPO:probinson[2020-07-14]
OMIM:614208	Intellectual developmental disorder, autosomal recessive 16		HP:0001250	OMIM:614208	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614208	Intellectual developmental disorder, autosomal recessive 16		HP:0000007	OMIM:614208	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614208	Intellectual developmental disorder, autosomal recessive 16		HP:0000664	OMIM:614208	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614208	Intellectual developmental disorder, autosomal recessive 16		HP:0001249	OMIM:614208	TAS					P	HPO:skoehler[2017-07-13]
OMIM:112350	Weismann-Netter syndrome		HP:0003510	PMID:21274295	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-06-19]
OMIM:112350	Weismann-Netter syndrome		HP:0002650	OMIM:112350	TAS					P	HPO:skoehler[2013-03-08]
OMIM:112350	Weismann-Netter syndrome		HP:0010538	OMIM:112350	TAS		HP:0040283			P	HPO:skoehler[2013-03-08]
OMIM:112350	Weismann-Netter syndrome		HP:0003440	OMIM:112350	TAS					P	HPO:skoehler[2013-03-08]
OMIM:112350	Weismann-Netter syndrome		HP:0003177	OMIM:112350	IEA					P	HPO:iea[2009-02-17]
OMIM:112350	Weismann-Netter syndrome		HP:0004490	OMIM:112350	TAS		HP:0040283			P	HPO:skoehler[2013-03-08]
OMIM:112350	Weismann-Netter syndrome		HP:0010502	PMID:21274295	PCS		2/2			P	HPO:probinson[2021-06-19]
OMIM:112350	Weismann-Netter syndrome		HP:0005090	PMID:21274295	PCS		2/2			P	HPO:probinson[2021-06-19]
OMIM:112350	Weismann-Netter syndrome		HP:0006390	PMID:21274295	PCS		2/2			P	HPO:probinson[2021-06-19]
OMIM:112350	Weismann-Netter syndrome		HP:0002808	OMIM:112350	TAS					P	HPO:skoehler[2013-03-08]
OMIM:112350	Weismann-Netter syndrome		HP:0000696	OMIM:112350	TAS		HP:0040283			P	HPO:skoehler[2013-03-08]
OMIM:112350	Weismann-Netter syndrome		HP:0000006	OMIM:112350	IEA					I	HPO:iea[2009-02-17]
OMIM:112350	Weismann-Netter syndrome		HP:0001249	OMIM:112350	IEA					P	HPO:iea[2009-02-17]
OMIM:615670	Schwannomatosis 2		HP:0100008	PMID:24362817	PCS		23/23			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-02]
OMIM:615670	Schwannomatosis 2		HP:0003581	PMID:24362817	PCS		23/23			C	HPO:probinson[2022-11-02]
OMIM:615670	Schwannomatosis 2		HP:0003829	PMID:24362817	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-02]
OMIM:615670	Schwannomatosis 2		HP:0010302	PMID:24362817	PCS					P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-02]
OMIM:615670	Schwannomatosis 2		HP:0000006	PMID:24362817	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-02]
OMIM:136580	Fragile site 16q22		HP:0005268	OMIM:136580	IEA					C	HPO:skoehler[2013-01-10]
OMIM:136580	Fragile site 16q22		HP:0002916	OMIM:136580	IEA					P	HPO:skoehler[2013-01-10]
OMIM:136580	Fragile site 16q22		HP:0000789	OMIM:136580	IEA					P	HPO:skoehler[2013-01-09]
OMIM:136580	Fragile site 16q22		HP:0002733	OMIM:136580	IEA					P	HPO:skoehler[2013-01-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000286	PMID:30595372	PCS		1/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002069	PMID:30595372	PCS		6/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002188	PMID:30595372	PCS		2/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002365	PMID:30595372	PCS		1/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000023	PMID:30595372	PCS		1/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000485	PMID:30595372	PCS		1/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002121	PMID:30595372	PCS		1/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0001252	PMID:30595372	PCS		11/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0003593	PMID:30595372	PCS		4/9			C	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0011463	PMID:30595372	PCS		2/9			C	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000316	PMID:30595372	PCS		1/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000954	PMID:30595372	PCS		5/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000337	PMID:30595372	PCS		2/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000733	PMID:30595372	PCS		1/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002119	PMID:30595372	PCS		4/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000218	PMID:30595372	PCS		2/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000455	PMID:30595372	PCS		3/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000256	PMID:30595372	PCS		2/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0003623	PMID:30595372	PCS		1/9			C	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000252	PMID:30595372	PCS		2/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0003621	PMID:30595372	PCS		2/9			C	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000750	PMID:30595372	PCS		10/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0031936	PMID:30595372	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002079	PMID:30595372	PCS		2/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002376	PMID:30595372	PCS		2/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0011968	PMID:30595372	PCS		9/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0001263	PMID:30595372	PCS		16/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0011623	PMID:30595372	PCS		1/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000729	PMID:30595372	PCS		5/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000629	PMID:30595372	PCS		2/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0001537	PMID:30595372	PCS		1/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000505	PMID:30595372	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0100716	PMID:30595372	PCS		1/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0007334	PMID:30595372	PCS		1/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0001357	PMID:30595372	PCS		3/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0002007	PMID:30595372	PCS		2/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000520	PMID:30595372	PCS		2/16			P	HPO:skoehler[2019-04-18]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000322	PMID:30595372	PCS		3/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0007018	PMID:30595372	PCS		2/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0007359	PMID:30595372	PCS		1/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0001631	PMID:30595372	PCS		1/16			P	HPO:probinson[2023-03-10]
OMIM:618354	Neurodevelopmental disorder and language delay with or without structural brain abnormalities		HP:0000006	PMID:30595372	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-10]
OMIM:610708	Optic atrophy 5		HP:0001133	PMID:28969390	PCS		3/4			P	HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0007924	PMID:28969390	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0003621	PMID:28969390	PCS		2/4			C	HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0000552	OMIM:610708	IEA					P	HPO:iea[2009-02-17]
OMIM:610708	Optic atrophy 5		HP:0003596	PMID:28969390	PCS		1/4			C	HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0030455	PMID:28969390	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0000648	PMID:28969390	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0000603	PMID:28969390	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0025710	PMID:28969390	PCS		1/4			C	HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0000543	PMID:28969390	PCS		4/4			P	HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0000006	PMID:28969390	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:610708	Optic atrophy 5		HP:0003677	PMID:28969390	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-04]
OMIM:620813	MHC class I deficiency 2		HP:0004798	PMID:36229627	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0002257	PMID:10560675;PMID:7517574	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0031691	PMID:10560675;PMID:7517574	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0002110	PMID:10560675	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0032230	PMID:10560675	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0011463	PMID:36229627;PMID:10560675	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0100582	PMID:10560675;PMID:7517574	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0000007	PMID:7517574	PCS					I	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0004429	PMID:7517574	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0011109	PMID:10560675;PMID:7517574	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0002205	PMID:36229627	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:620813	MHC class I deficiency 2		HP:0004469	PMID:10560675;PMID:7517574	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-24]
OMIM:609259	Myopia 10		HP:0000545	OMIM:609259	TAS					P	HPO:skoehler[2014-10-17]
OMIM:617073	Tooth agenesis, selective, 8		HP:0000958	PMID:27321946	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617073	Tooth agenesis, selective, 8		HP:0000691	PMID:27321946	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617073	Tooth agenesis, selective, 8		HP:0001592	PMID:27321946	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:617073	Tooth agenesis, selective, 8		HP:0045075	PMID:27321946	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617073	Tooth agenesis, selective, 8		HP:0000006	PMID:27321946	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:617073	Tooth agenesis, selective, 8		HP:0008070	PMID:27321946	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0003577	PMID:38503300	PCS		1/6			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0001596	PMID:38503300	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002583	PMID:38503300	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002240	PMID:38503300	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0003593	PMID:38503300	PCS		1/6			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0031545	PMID:38503300	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0001508	PMID:38503300	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002719	PMID:38503300	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002716	PMID:38503300	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0020102	PMID:38503300	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0000411	PMID:38503300	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0003623	PMID:38503300	PCS		4/6			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0005403	PMID:38503300	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002014	PMID:38503300	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002850	PMID:38503300	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0001880	PMID:38503300	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0010976	PMID:38503300	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0009098	PMID:38503300	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0031381	PMID:38503300	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0032132	PMID:38503300	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0033221	PMID:38503300	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0001999	PMID:38503300	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0001019	PMID:38503300	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0000307	PMID:38503300	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0000047	PMID:38503300	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002720	PMID:38503300	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0000006	PMID:38503300	PCS					I	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620807	Immunodeficiency 121 with autoinflammation		HP:0002721	PMID:38503300	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000365	PMID:21061399	PCS		27/73			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000023	PMID:21061399	PCS		26/53			P	HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001250	PMID:21061399	PCS		53/80			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001670	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0002240	PMID:21061399	PCS		10/110			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000280	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:4000193	OMIM:252900	TAS					P	HPO:probinson[2024-01-06]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001507	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0011463	PMID:21061399	PCS					C	HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0003309	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000752	PMID:21061399	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0002159	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001007	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001249	PMID:21061399	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001744	PMID:21061399	PCS		2/110			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0002014	PMID:21061399	PCS		59/72			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0002650	PMID:21061399	PCS		10/110			P	HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001387	OMIM:252900	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001263	PMID:21061399	PCS		72/76			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000250	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000943	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0001537	PMID:21061399	PCS		15/45			P	HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000007	PMID:21061399	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0002208	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000900	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0002788	PMID:21061399	PCS		61/70			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:252900	Mucopolysaccharidosis type IIIA		HP:0000664	OMIM:252900	IEA					P	HPO:iea[2009-02-17]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000582	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0001176	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000486	PMID:19136950	PCS	HP:0003593	1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0004322	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0004442	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0001252	PMID:19136950	PCS		3/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0010862	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0007021	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000817	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0009882	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000717	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000219	PMID:19136950	PCS		3/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0009765	PMID:19136950	PCS		3/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000218	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0001466	PMID:19136950	PCS					I	HPO:probinson[2024-12-27];HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0009748	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000098	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000252	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0001520	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000574	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000431	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0002650	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0002474	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000276	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000490	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0001263	PMID:19136950	PCS		5/7			P	HPO:probinson[2024-12-27];HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0002827	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000629	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000426	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000601	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000689	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0006167	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000722	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000527	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000664	PMID:19136950	PCS		3/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0004406	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000400	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0005616	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000322	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0007018	PMID:19136950	PCS		2/7			P	HPO:probinson[2024-12-27];HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000006	PMID:19136950	PCS					I	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000325	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000303	PMID:19136950	PCS		2/14			P	HPO:probinson[2024-12-27]
OMIM:613215	Chromosome 17p13.3 duplication syndrome		HP:0000347	PMID:19136950	PCS		1/7			P	HPO:probinson[2024-12-27]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0001792	OMIM:613573	TAS					P	HPO:probinson[2013-03-12]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0003577	PMID:20691405	PCS		6/6			C	HPO:probinson[2022-05-08]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0002232	OMIM:613573	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0001596	PMID:20691405	PCS		6/6		HP:0003676	P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0002046	OMIM:613573	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0002550	OMIM:613573	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0010709	PMID:20691405	PCS		3/6			P	HPO:probinson[2022-05-08]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0004692	PMID:20691405	PCS		2/6			P	HPO:probinson[2022-05-08]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0010554	OMIM:613573	TAS					P	HPO:probinson[2013-01-09]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0010765	OMIM:613573	TAS					P	HPO:probinson[2013-03-12]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0000968	OMIM:613573	TAS					P	HPO:skoehler[2015-01-14]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0005709	PMID:20691405	PCS		6/6			P	HPO:probinson[2013-03-12];HPO:probinson[2022-05-08]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0006297	OMIM:613573	TAS					P	HPO:probinson[2013-03-12]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0002209	OMIM:613573	TAS					P	HPO:probinson[2013-03-12]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0000007	PMID:20691405	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0001800	OMIM:613573	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0002208	OMIM:613573	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0000653	OMIM:613573	TAS					P	HPO:probinson[2013-03-12]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0000698	OMIM:613573	TAS					P	HPO:probinson[2013-03-12]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0003777	PMID:20691405	PCS		5/5			P	HPO:probinson[2013-03-12];HPO:probinson[2022-05-08]
OMIM:613573	Ectodermal dysplasia-syndactyly syndrome 1		HP:0000687	OMIM:613573	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615102	Tyshchenko syndrome		HP:0000189	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0004322	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0001629	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000218	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000774	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0001642	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0002558	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000358	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0001622	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000175	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0001561	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000331	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0002079	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0011968	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0001263	OMIM:615102	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:615102	Tyshchenko syndrome		HP:0000294	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0010535	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0100874	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000508	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000767	OMIM:615102	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:615102	Tyshchenko syndrome		HP:0002705	OMIM:615102	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615102	Tyshchenko syndrome		HP:0001511	OMIM:615102	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615102	Tyshchenko syndrome		HP:0001631	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000520	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000028	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000369	OMIM:615102	TAS					P	HPO:skoehler[2013-03-22]
OMIM:615102	Tyshchenko syndrome		HP:0000006	OMIM:615102	TAS					I	HPO:skoehler[2013-03-22]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002487	PMID:31970218	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001276	PMID:34890876	PCS		4/4			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002345	PMID:34890876	PCS		6/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001332	PMID:29120065;PMID:31970218;PMID:34890876	PCS		8/8			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001272	PMID:31970218	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002283	PMID:29120065	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001251	PMID:34890876	PCS		3/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0000716	PMID:34890876	PCS		2/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0011463	PMID:29120065;PMID:31970218;PMID:34890876	PCS		4/8			C	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0000718	PMID:34890876	PCS		1/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0000739	PMID:34890876	PCS		2/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001249	PMID:34890876	PCS		3/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001622	PMID:29120065	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0003623	PMID:34890876	PCS		1/6			C	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0003621	PMID:34890876	PCS		3/6			C	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002015	PMID:34890876	PCS		1/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002474	PMID:29120065	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001300	PMID:29120065;PMID:34890876	PCS		3/7			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002376	PMID:31970218	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002072	PMID:31970218;PMID:34890876	PCS		3/7			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0100660	PMID:29120065	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0000709	PMID:34890876	PCS		2/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0012760	PMID:34890876	PCS		1/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0000007	PMID:29120065	PCS					I	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0025403	PMID:29120065	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0002107	PMID:29120065	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001510	PMID:34890876	PCS		2/6			P	HPO:probinson[2022-04-05]
OMIM:619738	Parkinsonism-dystonia 3, childhood-onset		HP:0001337	PMID:29120065	PCS		1/1			P	HPO:probinson[2022-04-05]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0003642	OMIM:300934	TAS					P	HPO:skoehler[2015-01-04]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000154	PMID:26264460	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0003577	OMIM:300934	TAS					C	HPO:skoehler[2015-12-30]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000252	PMID:26264460	PCS		9/9			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0002650	OMIM:300934	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000486	PMID:26264460	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0002079	OMIM:300934	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0011968	PMID:26264460	PCS		8/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0002098	OMIM:300934	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001250	PMID:26264460	PCS		5/9		HP:0012825	P	HPO:skoehler[2015-01-04];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000490	PMID:26264460	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001263	PMID:26264460	PCS		9/9			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001252	PMID:26264460	PCS		9/9			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001373	OMIM:300934	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001290	OMIM:300934	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001508	PMID:26264460	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001419	PMID:26264460	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001928	OMIM:300934	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0030084	OMIM:300934	TAS					P	HPO:skoehler[2015-01-04]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000400	PMID:26264460	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000047	OMIM:300934	TAS				HP:0012825	P	HPO:skoehler[2015-01-04]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0001249	PMID:26264460	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000347	OMIM:300934	TAS					P	HPO:skoehler[2015-01-04]
OMIM:300934	Congenital disorder of glycosylation, type Iy		HP:0000687	PMID:26264460	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:611364	Myoclonic epilepsy, juvenile, susceptibility to, 4		HP:0002069	PMID:17431681	PCS		7/9			P	HPO:skoehler[2010-06-19]
OMIM:611364	Myoclonic epilepsy, juvenile, susceptibility to, 4		HP:0003621	PMID:17431681	PCS		8/8			C	HPO:probinson[2024-03-14]
OMIM:611364	Myoclonic epilepsy, juvenile, susceptibility to, 4		HP:0002123	PMID:17431681	PCS		9/9			P	HPO:skoehler[2010-06-20]
OMIM:611364	Myoclonic epilepsy, juvenile, susceptibility to, 4		HP:0002373	PMID:17431681	PCS		0/8			P	HPO:lccarmody[2018-06-27];HPO:probinson[2024-03-14]
OMIM:611364	Myoclonic epilepsy, juvenile, susceptibility to, 4		HP:0002121	PMID:17431681	PCS		0/8			P	HPO:lccarmody[2018-06-27];HPO:probinson[2024-03-14]
OMIM:611364	Myoclonic epilepsy, juvenile, susceptibility to, 4		HP:0002392	PMID:17431681	PCS		6/8			P	HPO:lccarmody[2018-06-27]
OMIM:611364	Myoclonic epilepsy, juvenile, susceptibility to, 4		HP:0000006	PMID:17431681	PCS					I	HPO:skoehler[2010-06-19]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001276	PMID:30758658	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002069	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0003676	PMID:30758658	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002783	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001250	PMID:30758658	PCS		3/3		HP:0031375	P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001272	OMIM:618426	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001252	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002283	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002020	PMID:30758658	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001251	OMIM:618426	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001290	PMID:30758658	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0040213	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001508	PMID:30758658	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001522	PMID:30758658	PCS		1/3			C	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0003623	PMID:30758658	PCS		2/3			C	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001347	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0000252	PMID:30758658	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002059	OMIM:618426	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002013	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002376	PMID:30758658	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002098	OMIM:618426	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0011968	PMID:30758658	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002033	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001263	PMID:30758658	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0012510	PMID:30758658	PCS		2/3			P	HPO:probinson[2022-12-20];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0003819	PMID:30758658	PCS		2/3			C	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002902	PMID:30758658	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0000007	PMID:30758658	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002900	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0000961	PMID:30758658	PCS		1/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001257	OMIM:618426	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002643	PMID:30758658	PCS		2/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0002104	PMID:30758658	PCS		3/3			P	HPO:probinson[2022-12-20]
OMIM:618426	Encephalopathy, acute, infection-induced, susceptibility to, 9		HP:0001336	OMIM:618426	IEA					P	HPO:skoehler[2019-09-07]
OMIM:600269	Short tarsus with absence of lower eyelashes		HP:0007697	OMIM:600269	IEA					P	HPO:iea[2009-02-17]
OMIM:600269	Short tarsus with absence of lower eyelashes		HP:0000006	OMIM:600269	IEA					I	HPO:iea[2009-02-17]
OMIM:600269	Short tarsus with absence of lower eyelashes		HP:0007646	OMIM:600269	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0005469	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0008738	OMIM:181510	TAS					P	HPO:probinson[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0004322	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0000086	OMIM:181510	TAS					P	HPO:probinson[2014-01-18]
OMIM:181510	Schizophrenia 1		HP:0100396	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0100753	OMIM:181510	TAS					P	HPO:probinson[2012-09-18]
OMIM:181510	Schizophrenia 1		HP:0000738	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0007086	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0000316	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0000746	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0000411	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0002007	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:181510	Schizophrenia 1		HP:0001159	OMIM:181510	IEA					P	HPO:skoehler[2018-10-08]
OMIM:181510	Schizophrenia 1		HP:0000006	OMIM:181510	TAS					I	HPO:skoehler[2013-05-29]
OMIM:181510	Schizophrenia 1		HP:0000104	OMIM:181510	IEA					P	HPO:iea[2009-02-17]
OMIM:612645	Deafness, autosomal recessive 1B		HP:0001751	OMIM:612645	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612645	Deafness, autosomal recessive 1B		HP:0000365	OMIM:612645	IEA					P	HPO:skoehler[2015-01-27]
OMIM:612645	Deafness, autosomal recessive 1B		HP:0000007	OMIM:612645	TAS					I	HPO:skoehler[2012-10-17]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0003621	PMID:19561605	PCS		13/33			C	HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0003596	PMID:19561605	PCS		1/33			C	HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0003352	OMIM:224100	IEA					P	HPO:iea[2009-02-17]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0003584	PMID:19561605	PCS		1/33			C	HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0003593	PMID:19561605	PCS		6/33			C	HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0001081	OMIM:224100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0010972	PMID:19561605	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0011463	PMID:19561605	PCS		4/33			C	HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0011462	PMID:19561605	PCS		8/33			C	HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0000007	PMID:19561605	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0001923	PMID:19561605	PCS		19/33			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-07-19]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0000952	OMIM:224100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0001744	OMIM:224100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:224100	Anemia, dyserythropoietic congenital, type II		HP:0003655	OMIM:224100	IEA					P	HPO:iea[2009-02-17]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000286	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000343	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000540	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001992	PMID:33979636	PCS		0/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001250	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001252	PMID:33979636	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001251	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0004780	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0003593	PMID:33979636	PCS		4/4			C	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0005274	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0011856	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0010801	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0006191	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000958	PMID:33979636	PCS		4/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0008593	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000319	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000718	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000414	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000219	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0012071	PMID:33979636	PCS		0/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000218	PMID:33979636	PCS		6/8			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001324	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000411	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001249	PMID:33979636	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0009748	PMID:33979636	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000577	PMID:33979636	PCS		4/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000396	PMID:33979636	PCS		2/8			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000494	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000670	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000750	PMID:33979636	PCS		4/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0002133	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0031936	PMID:33979636	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001382	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001263	PMID:33979636	PCS		4/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0003160	PMID:33979636	PCS		0/3			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0005280	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0032152	PMID:33979636	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000448	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000007	PMID:33979636	PCS					I	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000964	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000527	PMID:33979636	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0000307	PMID:33979636	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620191	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities		HP:0001513	PMID:33979636	PCS	HP:0011463	3/4			P	HPO:probinson[2023-06-11]
OMIM:609265	Li-Fraumeni syndrome 2		HP:0003002	PMID:11479205	PCS					P	HPO:probinson[2013-01-09]
OMIM:609265	Li-Fraumeni syndrome 2		HP:0002858	PMID:11479205	PCS					P	HPO:probinson[2013-03-26]
OMIM:609265	Li-Fraumeni syndrome 2		HP:0009733	PMID:10617473	PCS					P	HPO:probinson[2013-03-26]
OMIM:609265	Li-Fraumeni syndrome 2		HP:0012126	PMID:11479205	PCS					P	HPO:probinson[2013-03-26]
OMIM:609265	Li-Fraumeni syndrome 2		HP:0000006	PMID:10617473	PCS					I	HPO:probinson[2013-03-26]
OMIM:609265	Li-Fraumeni syndrome 2		HP:0100242	PMID:10617473	PCS					P	HPO:probinson[2013-03-26]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001276	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0002521	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0002188	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001250	PMID:32103185	PCS	HP:0003593	3/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001371	PMID:32103185	PCS		2/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001252	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0032794	PMID:32103185	PCS	HP:0003593	1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0012444	PMID:32103185	PCS					P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000737	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001324	PMID:32103185	PCS		2/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000311	PMID:32103185	PCS		2/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000577	PMID:32103185	PCS		2/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001347	PMID:32103185	PCS		3/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000252	PMID:32103185	PCS		3/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001363	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0002079	PMID:32103185	PCS		3/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0025190	PMID:32103185	PCS	HP:0003593	1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0011344	PMID:32103185	PCS		3/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0011421	PMID:32103185	PCS		1/3			C	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0002190	PMID:32103185	PCS	HP:0003593	1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000508	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000007	PMID:32103185	PCS					I	HPO:probinson[2020-12-13];HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000527	PMID:32103185	PCS		2/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0000543	PMID:32103185	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:619076	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy		HP:0001257	PMID:32103185	PCS		3/3			P	HPO:probinson[2020-12-13]
OMIM:616345	Immunodeficiency 39		HP:0011463	PMID:25814066	PCS		1/1			C	HPO:probinson[2022-04-12]
OMIM:616345	Immunodeficiency 39		HP:0000007	PMID:25814066	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616345	Immunodeficiency 39		HP:0034249	PMID:25814066	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:616345	Immunodeficiency 39		HP:0002721	PMID:25814066	PCS					P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0003577	PMID:9020846	PCS		9/9			C	HPO:probinson[2022-04-30]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0000007	PMID:9020846	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0001657	OMIM:220400	IEA					P	HPO:iea[2009-02-17]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0005184	PMID:9020846	PCS		9/9			P	HPO:probinson[2022-04-30]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0001279	PMID:9020846	PCS		9/9		HP:0031796	P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0001664	OMIM:220400	IEA					P	HPO:iea[2009-02-17]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0001645	OMIM:220400	IEA					P	HPO:iea[2009-02-17]
OMIM:220400	Jervell and Lange-Nielsen syndrome 1		HP:0008527	PMID:9020846	PCS	HP:0003577	9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0011939	PMID:16816024	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000286	OMIM:257850	TAS					P	HPO:probinson[2018-01-25]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000684	PMID:16816024	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0001773	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0004322	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000160	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000482	OMIM:257850	TAS					P	HPO:iea[2009-02-17]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0012745	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000518	PMID:16816024	PCS		1/2			P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0011342	OMIM:257850	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000239	PMID:16816024	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000678	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000675	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0005769	OMIM:257850	TAS					P	HPO:iea[2009-02-17]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0005768	OMIM:257850	TAS					P	HPO:iea[2009-02-17]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0009748	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0005622	OMIM:257850	TAS					P	HPO:skoehler[2012-10-17]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000494	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0002750	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000490	PMID:16816024	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0001263	PMID:16816024	PCS		1/2		HP:0012825	P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0002194	PMID:16816024	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000327	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000007	PMID:16816024	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000689	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000568	PMID:16816024	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000685	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000248	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000369	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0010705	OMIM:257850	TAS					P	HPO:iea[2009-02-17]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0003577	PMID:16816024	PCS		2/2			C	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000343	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0009917	PMID:16816024	PCS		1/2			P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000460	OMIM:257850	TAS					P	HPO:skoehler[2013-08-11]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0008070	PMID:16816024	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0001508	PMID:16816024	PCS		1/2			P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0006334	PMID:16816024	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000653	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0002213	PMID:16816024	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000750	PMID:16816024	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0003189	OMIM:257850	TAS					P	HPO:skoehler[2013-08-11]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000233	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000430	PMID:16816024	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0010537	PMID:16816024	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000506	OMIM:257850	TAS					P	HPO:iea[2009-02-17]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0002007	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0200055	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000347	PMID:16816024	PCS		2/2			P	HPO:skoehler[2015-02-22];HPO:probinson[2023-05-19]
OMIM:257850	Oculodentodigital dysplasia, autosomal recessive		HP:0000545	OMIM:257850	TAS					P	HPO:skoehler[2015-02-22]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0000572	PMID:23479643	PCS	HP:0011463	2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0003487	PMID:23479643	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0031936	PMID:23479643	PCS	HP:0011463	2/2			P	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0003474	PMID:23479643	PCS		0/2			P	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0002061	PMID:23479643	PCS	HP:0011463	2/2			P	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0009130	PMID:23479643	PCS		2/2			P	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0011463	PMID:23479643	PCS		2/2			C	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0007220	PMID:23479643	PCS		2/2			P	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0007210	PMID:23479643	PCS		2/2			P	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0000007	PMID:23479643	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0000648	PMID:23479643	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0002505	PMID:23479643	PCS	HP:0003621	2/2			P	HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0001258	PMID:23479643	PCS		2/2			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0001324	PMID:23479643	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-08]
OMIM:615658	Spastic paraplegia 57, autosomal recessive		HP:0001347	PMID:23479643	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-08]
OMIM:113700	Breasts and/or nipples, aplasia or hypoplasia of, 1		HP:0100853	OMIM:113700	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:113700	Breasts and/or nipples, aplasia or hypoplasia of, 1		HP:0000453	OMIM:113700	TAS		HP:0040283			P	HPO:skoehler[2014-09-21]
OMIM:113700	Breasts and/or nipples, aplasia or hypoplasia of, 1		HP:0002561	OMIM:113700	TAS					P	HPO:skoehler[2015-01-04]
OMIM:113700	Breasts and/or nipples, aplasia or hypoplasia of, 1		HP:0006709	OMIM:113700	IEA					P	HPO:iea[2012-02-21]
OMIM:113700	Breasts and/or nipples, aplasia or hypoplasia of, 1		HP:0010311	OMIM:113700	IEA					P	HPO:iea[2009-02-17]
OMIM:113700	Breasts and/or nipples, aplasia or hypoplasia of, 1		HP:0001417	OMIM:113700	TAS					I	HPO:skoehler[2012-11-17]
OMIM:113700	Breasts and/or nipples, aplasia or hypoplasia of, 1		HP:0000006	OMIM:113700	TAS					I	HPO:skoehler[2012-11-16]
OMIM:155755	Melanoma-Astrocytoma syndrome		HP:0012056	OMIM:155755	TAS					P	HPO:probinson[2009-02-17]
OMIM:155755	Melanoma-Astrocytoma syndrome		HP:0009592	OMIM:155755	TAS					P	HPO:skoehler[2010-06-20]
OMIM:155755	Melanoma-Astrocytoma syndrome		HP:0000006	OMIM:155755	TAS					I	HPO:probinson[2009-02-17]
OMIM:613229	TRICHOTILLOMANIA		HP:0012167	OMIM:613229	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613229	TRICHOTILLOMANIA		HP:0001596	OMIM:613229	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613229	TRICHOTILLOMANIA		HP:0000722	OMIM:613229	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613229	TRICHOTILLOMANIA		HP:0001426	OMIM:613229	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613229	TRICHOTILLOMANIA		HP:0000006	OMIM:613229	IEA					I	HPO:skoehler[2010-06-19]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0003577	PMID:31155743	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0003542	PMID:31155743	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0002151	PMID:31155743	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0003593	PMID:31155743	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0001290	PMID:31155743	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0030319	PMID:31155743	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0012240	PMID:31155743	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0000007	PMID:31155743	PCS					I	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0008347	PMID:31155743	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0000218	PMID:31155743	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0001324	PMID:31155743	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0002643	PMID:31155743	PCS	HP:0003577	1/2			P	HPO:probinson[2020-12-08]
OMIM:619062	Mitochondrial complex IV deficiency, nuclear type 18		HP:0003688	PMID:31155743	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0002069	PMID:25533962	PCS		2/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000286	PMID:25533962	PCS		2/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000582	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000365	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0001773	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000463	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0100704	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000319	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000733	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0006610	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0001488	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0001249	PMID:25533962	PCS		3/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0003763	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0002212	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0008936	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0002058	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0001562	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0002136	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0001263	PMID:25533962	PCS		3/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0005484	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0004691	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0002208	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0002307	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000664	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000006	PMID:25533962	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616351	Neurodevelopmental disorder with hypotonia, speech delay, and dysmorphic facies		HP:0000687	PMID:25533962	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0003202	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0001265	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0002366	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0002300	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0002015	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0003676	OMIM:616437	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0002463	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0002145	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0002120	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0001283	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0001260	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0002380	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0000734	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0007354	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0001324	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0000741	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0000751	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0000006	OMIM:616437	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616437	Frontotemporal dementia and/or amyotrophic lateral sclerosis 3		HP:0001347	OMIM:616437	TAS					P	HPO:skoehler[2015-07-26]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0020082	PMID:29298156	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0003577	PMID:9674740	PCS		3/19			C	HPO:probinson[2021-11-27];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0003621	PMID:9674740	PCS		3/19			C	HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0003596	PMID:9674740	PCS		1/19			C	HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0003641	OMIM:300908	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0000980	OMIM:300908	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0410179	PMID:9674740	PCS		20/20			P	HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0003593	PMID:9674740	PCS		4/19			C	HPO:probinson[2021-11-27];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0008282	PMID:9674740	PCS					P	HPO:probinson[2014-01-04];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0011273	OMIM:300908	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0011463	PMID:9674740	PCS		7/19			C	HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0011462	PMID:9674740	PCS		1/19			C	HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0001923	PMID:9674740	PCS					P	HPO:probinson[2014-01-04];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0004814	PMID:29298156;PMID:9674740	PCS		16/16		HP:0034060	P	HPO:probinson[2014-01-04];HPO:probinson[2021-11-27];HPO:probinson[2022-04-15]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0001945	OMIM:300908;PMID:29298156	PCS		11/11		HP:0034060	P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-15]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0001423	PMID:29298156	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0006579	PMID:9674740	PCS		19/19			P	HPO:probinson[2014-01-04];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0002027	OMIM:300908;PMID:29298156	PCS		11/11		HP:0034060	P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-15]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0001744	PMID:9674740	PCS		17/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-11-27]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0000952	PMID:29298156	PCS		1/1		HP:0034060	P	HPO:probinson[2022-04-15]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0001974	OMIM:300908	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300908	Hemolytic anemia, G6PD deficient (favism)		HP:0004447	OMIM:300908	IEA					P	HPO:skoehler[2018-10-08]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0000164	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0002653	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0003324	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0004322	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0003155	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0003829	OMIM:193100	IEA					I	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0002748	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0002814	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0000117	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0002749	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0004912	OMIM:193100	IEA					P	HPO:skoehler[2015-01-27]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0000006	OMIM:193100	IEA					I	HPO:iea[2009-02-17]
OMIM:193100	Hypophosphatemic rickets, autosomal dominant		HP:0002148	OMIM:193100	IEA					P	HPO:iea[2009-02-17]
OMIM:620185	Atelis syndrome 2		HP:0001298	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000286	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0030752	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001310	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001250	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0002020	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0012745	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001270	PMID:36333305	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001903	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000739	PMID:36333305	PCS		3/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000519	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000954	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000414	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0030084	PMID:36333305	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0002714	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000218	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001643	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000411	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001763	PMID:36333305	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001642	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000179	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001348	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000699	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000252	PMID:36333305	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0007968	PMID:36333305	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0007902	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000771	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000276	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0002094	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0034349	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0002808	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000448	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000007	PMID:36333305	PCS					I	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0002925	PMID:36333305	PCS		2/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000568	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0002007	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0007018	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000960	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0001873	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000842	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000369	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000347	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:620185	Atelis syndrome 2		HP:0000325	PMID:36333305	PCS		1/4			P	HPO:probinson[2023-06-11]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000286	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000486	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0004322	OMIM:617729	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001250	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000160	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001252	PMID:28272532	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0003073	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000639	PMID:28272532	PCS		2/2			P	HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000316	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001967	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001249	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0002036	OMIM:617729	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000494	PMID:28272532	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000252	PMID:28272532	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0002079	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000490	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001263	PMID:28272532	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000096	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0011800	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000093	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0012385	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000969	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0002827	OMIM:617729	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001339	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000767	PMID:28272532	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000007	PMID:28272532	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000568	PMID:28272532	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001257	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000369	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000341	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0003774	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000340	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0003577	PMID:28272532	PCS		2/2			C	HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000100	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001272	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001508	PMID:28272532	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0002119	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000218	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001302	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001166	PMID:28272532	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001562	OMIM:617729	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0002059	PMID:28272532	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000750	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001680	PMID:28272532	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000822	PMID:28272532	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000505	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0001511	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0002007	PMID:28272532	PCS		1/2			P	HPO:probinson[2023-02-25]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0000347	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617729	Galloway-Mowat syndrome 3		HP:0009879	OMIM:617729	IEA					P	HPO:skoehler[2018-10-08]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0000494	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0004467	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0000384	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0002023	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0004322	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0000612	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0001627	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0000347	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:42	Cat-Eye Syndrome (Type I)		HP:0001249	DECIPHER:42	IEA					P	HPO:skoehler[2013-05-29]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001331	PMID:19185282	PCS		2/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0002982	PMID:19185282	PCS		2/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0002983	PMID:19185282	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000046	PMID:19185282	PCS		1/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000161	PMID:19185282	PCS		4/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0007360	PMID:19185282	PCS		1/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0004719	OMIM:612651	IEA					P	HPO:skoehler[2019-09-07]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000437	PMID:19185282	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000954	PMID:19185282	PCS		3/3			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000238	PMID:19185282	PCS		2/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000835	PMID:19185282	PCS		2/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0030260	PMID:19185282	PCS		3/4			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000695	OMIM:612651	IEA					P	HPO:skoehler[2019-09-07]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000490	PMID:19185282	PCS		5/5			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0011800	PMID:19185282	PCS		6/6			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0100336	PMID:19185282	PCS		2/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0100259	PMID:19185282	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0100258	OMIM:612651	IEA					P	HPO:skoehler[2019-09-07]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0009099	PMID:19185282	PCS		5/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000007	PMID:19185282	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000601	PMID:19185282	PCS		1/1			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0003956	PMID:19185282	PCS		6/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001852	PMID:19185282	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000047	PMID:19185282	PCS		1/4	MALE		P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000369	PMID:19185282	PCS		4/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0008749	PMID:19185282	PCS		2/3			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001234	PMID:19185282	PCS		1/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001552	PMID:19185282	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001156	PMID:19185282	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000062	OMIM:612651	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0030674	PMID:19185282	PCS		6/6			C	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001274	PMID:19185282	PCS		1/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0010502	PMID:19185282	PCS		2/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0009487	PMID:19185282	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0002119	PMID:19185282	PCS		2/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000774	PMID:19185282	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0006610	PMID:19185282	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000215	PMID:19185282	PCS		2/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0005349	PMID:19185282	PCS		2/3			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001561	PMID:19185282	PCS		1/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001762	PMID:19185282	PCS		0/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000431	PMID:19185282	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001360	PMID:19185282	PCS		3/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0032466	PMID:19185282	PCS		1/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0012245	PMID:19185282	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0032471	PMID:19185282	PCS		1/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0009755	PMID:19185282	PCS		4/4			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000268	PMID:19185282	PCS		3/6			P	HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0001159	PMID:19185282	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000028	PMID:19185282	PCS		1/4	MALE		P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000105	OMIM:612651	IEA					P	HPO:skoehler[2019-09-07]
OMIM:612651	ENDOCRINE-CEREBROOSTEODYSPLASIA		HP:0000347	PMID:19185282	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-10-13]
OMIM:191850	Urticaria, aquagenic		HP:0001025	OMIM:191850	TAS					P	HPO:skoehler[2009-02-17]
OMIM:191850	Urticaria, aquagenic		HP:0000006	OMIM:191850	IEA					I	HPO:iea[2009-02-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0001320	OMIM:612916	TAS					P	HPO:skoehler[2012-11-18]
OMIM:612916	Zechi-Ceide syndrome		HP:0000175	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0001792	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0000431	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0000430	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0011815	OMIM:612916	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612916	Zechi-Ceide syndrome		HP:0000581	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0000272	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0012745	OMIM:612916	TAS					P	HPO:skoehler[2014-03-24]
OMIM:612916	Zechi-Ceide syndrome		HP:0045025	OMIM:612916	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612916	Zechi-Ceide syndrome		HP:0011800	OMIM:612916	TAS					P	HPO:skoehler[2013-11-28]
OMIM:612916	Zechi-Ceide syndrome		HP:0010743	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0011220	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0009882	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0001999	OMIM:612916	IEA					P	HPO:skoehler[2015-12-30]
OMIM:612916	Zechi-Ceide syndrome		HP:0000007	OMIM:612916	TAS					I	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0001833	OMIM:612916	IEA					P	HPO:skoehler[2015-01-20]
OMIM:612916	Zechi-Ceide syndrome		HP:0001852	OMIM:612916	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612916	Zechi-Ceide syndrome		HP:0000402	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0000204	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0000677	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0001249	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612916	Zechi-Ceide syndrome		HP:0000445	OMIM:612916	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162700	Neutropenia, chronic familial		HP:0000230	OMIM:162700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162700	Neutropenia, chronic familial		HP:0006480	OMIM:162700	IEA					P	HPO:iea[2009-02-17]
OMIM:162700	Neutropenia, chronic familial		HP:0000704	OMIM:162700	IEA					P	HPO:iea[2009-02-17]
OMIM:162700	Neutropenia, chronic familial		HP:0100759	OMIM:162700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162700	Neutropenia, chronic familial		HP:0001217	OMIM:162700	IEA					P	HPO:iea[2009-02-17]
OMIM:162700	Neutropenia, chronic familial		HP:0010702	OMIM:162700	IEA					P	HPO:iea[2009-02-17]
OMIM:162700	Neutropenia, chronic familial		HP:0000006	OMIM:162700	TAS					I	HPO:skoehler[2013-05-29]
OMIM:162700	Neutropenia, chronic familial		HP:0001875	OMIM:162700	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0002144	PMID:25394726	PCS		1/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0004322	PMID:25394726	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0003396	PMID:25394726	PCS		3/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0003199	PMID:25394726	PCS		3/4			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0001252	PMID:25394726	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0003194	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0000319	OMIM:130720	TAS					P	HPO:probinson[2012-05-01]
OMIM:130720	Lateral meningocele syndrome		HP:0001647	PMID:25394726	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000316	PMID:25394726	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000678	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0000238	PMID:25394726	PCS		1/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0001643	PMID:25394726	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000358	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0001249	PMID:25394726	PCS		1/5			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000011	PMID:25394726	PCS		1/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000494	PMID:25394726	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000175	PMID:25394726	PCS		1/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0002870	PMID:25394726	PCS		3/4			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0001382	PMID:25394726	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0004452	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0001263	PMID:25394726	PCS		6/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0100775	OMIM:130720	TAS					P	HPO:skoehler[2012-10-17]
OMIM:130720	Lateral meningocele syndrome		HP:0010562	PMID:25394726	PCS		4/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0002948	PMID:25394726	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000767	PMID:25394726	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0001537	PMID:25394726	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000405	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0000006	PMID:25394726	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000369	PMID:25394726	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0001611	PMID:25394726	PCS		4/4			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0003577	PMID:25394726	PCS		6/6			C	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000343	OMIM:130720	TAS					P	HPO:probinson[2012-05-01]
OMIM:130720	Lateral meningocele syndrome		HP:0004586	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0000023	PMID:25394726	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0002684	PMID:25394726	PCS		2/4			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0001270	OMIM:130720	TAS					P	HPO:skoehler[2015-12-30]
OMIM:130720	Lateral meningocele syndrome		HP:0001629	PMID:25394726	PCS		2/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0100702	OMIM:130720	TAS					P	HPO:skoehler[2012-10-17]
OMIM:130720	Lateral meningocele syndrome		HP:0000218	PMID:25394726	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0002435	OMIM:130720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:130720	Lateral meningocele syndrome		HP:0002694	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0002650	PMID:25394726	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000272	PMID:25394726	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0002691	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0000470	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0002808	OMIM:130720	IEA					P	HPO:iea[2009-02-17]
OMIM:130720	Lateral meningocele syndrome		HP:0000506	PMID:25394726	PCS		2/6			P	HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0007099	PMID:25394726	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000508	PMID:25394726	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0002208	PMID:25394726	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000268	OMIM:130720	TAS					P	HPO:skoehler[2015-12-30]
OMIM:130720	Lateral meningocele syndrome		HP:0002645	PMID:25394726	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000028	PMID:25394726	PCS		4/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0000347	PMID:25394726	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:130720	Lateral meningocele syndrome		HP:0004942	PMID:25394726	PCS		2/6			P	HPO:probinson[2022-12-18]
OMIM:606963	Pulmonary disease, chronic obstructive		HP:0006510	OMIM:606963	TAS					P	HPO:skoehler[2013-01-09]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000362	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0001385	PMID:36338653	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000365	OMIM:166200	TAS	HP:0003581				P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0002980	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0003321	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:6001053	PMID:37189540	PCS					P	HPO:probinson[2024-08-03]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0001382	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000592	PMID:36338653	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0003593	PMID:36338653	PCS		1/1			C	HPO:probinson[2023-06-11]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0006094	PMID:36338653	PCS		1/1			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0001507	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000938	OMIM:166200	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0002757	PMID:36338653	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000703	OMIM:166200	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000978	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0002659	PMID:36338653	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-11]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0002645	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000963	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0001634	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0000006	OMIM:166200	IEA					I	HPO:iea[2009-02-17]
OMIM:166200	Osteogenesis imperfecta, type I		HP:0004942	OMIM:166200	IEA					P	HPO:iea[2009-02-17]
OMIM:276901	Usher syndrome, type IIA		HP:0000007	OMIM:276901	IEA					I	HPO:iea[2009-02-17]
OMIM:276901	Usher syndrome, type IIA		HP:0000510	OMIM:276901	IEA					P	HPO:iea[2009-02-17]
OMIM:276901	Usher syndrome, type IIA		HP:0008527	OMIM:276901	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003477	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003676	OMIM:218000	IEA					C	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0002540	PMID:16606917	PCS		1/3			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003431	OMIM:218000	TAS					P	HPO:probinson[2012-04-18]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001250	PMID:16606917	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001371	OMIM:218000	TAS					P	HPO:probinson[2012-04-18]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003196	PMID:16606917	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001252	PMID:16606917	PCS		2/3			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0011182	PMID:16606917	PCS		4/5			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000316	PMID:16606917	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0100807	OMIM:218000	TAS					P	HPO:probinson[2013-04-09]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0007204	PMID:16606917	PCS		1/3			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001249	OMIM:218000	TAS					P	HPO:probinson[2012-04-18]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003623	PMID:16606917	PCS		1/1			C	HPO:probinson[2022-11-03];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003202	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003444	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001344	PMID:16606917	PCS		1/3			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0011968	PMID:16606917	PCS		1/3			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001263	PMID:16606917	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000294	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0004691	OMIM:218000	TAS					P	HPO:probinson[2012-04-18]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001182	OMIM:218000	TAS					P	HPO:probinson[2013-04-09]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000327	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000007	PMID:12368912	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000763	OMIM:218000	TAS					P	HPO:probinson[2012-04-18]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000400	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000565	PMID:16606917	PCS		1/3			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000762	PMID:16606917	PCS		1/1			P	HPO:probinson[2022-11-03];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001337	OMIM:218000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000248	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000324	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000341	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003378	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001271	OMIM:218000	TAS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001274	PMID:16606917	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003690	OMIM:218000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001270	OMIM:218000	TAS					P	HPO:probinson[2012-04-18]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001349	PMID:16606917	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0002119	PMID:16606917	PCS		1/3			P	HPO:probinson[2012-04-18];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000218	PMID:16606917	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003448	OMIM:218000	TAS					P	HPO:probinson[2012-04-18]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0200085	OMIM:218000	TAS					P	HPO:skoehler[2013-06-04]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0007108	PMID:16606917	PCS					P	HPO:probinson[2022-11-03];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000431	PMID:16606917	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0002650	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000276	PMID:16606917	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0011947	OMIM:218000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0003383	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001284	PMID:16606917	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0002091	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000709	OMIM:218000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0000508	PMID:16606917	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0009830	PMID:16606917	PCS		2/3			P	HPO:probinson[2022-11-03]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0007178	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0001319	OMIM:218000	IEA					P	HPO:iea[2009-02-17]
OMIM:218000	Agenesis of the corpus callosum with peripheral neuropathy		HP:0002922	PMID:16606917	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0003236	OMIM:255100	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0002015	OMIM:255100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0002650	OMIM:255100	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0001992	OMIM:255100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0003198	OMIM:255100	TAS					P	HPO:skoehler[2010-06-18]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0011968	OMIM:255100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0003593	PMID:24311462	PCS		1/1			C	HPO:probinson[2023-04-04]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0001290	OMIM:255100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0012548	OMIM:255100	TAS					P	HPO:probinson[2014-01-01]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0002093	PMID:24311462	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-04]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0011923	PMID:24311462	PCS		1/1			P	HPO:probinson[2023-04-04]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0000007	PMID:24311462	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-04]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0008347	PMID:24311462	PCS		1/1			P	HPO:probinson[2023-04-04]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0001638	OMIM:255100	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0003701	OMIM:255100	TAS					P	HPO:probinson[2014-01-01]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0004755	OMIM:255100	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:255100	Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency		HP:0003546	OMIM:255100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618591	Short sleep, familial natural, 2		HP:0033063	PMID:31473062	PCS		6/7			P	HPO:probinson[2020-08-13]
OMIM:618591	Short sleep, familial natural, 2		HP:0000006	PMID:31473062	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0002015	OMIM:608782	IEA					P	HPO:iea[2009-02-17]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0001250	OMIM:608782	IEA					P	HPO:iea[2009-02-17]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0011968	PMID:15855260	PCS		2/2			P	HPO:probinson[2023-05-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0002066	OMIM:608782	IEA					P	HPO:iea[2009-02-17]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0001252	PMID:15855260	PCS	HP:0003623	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0001263	PMID:15855260	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0001290	OMIM:608782	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0000639	OMIM:608782	IEA					P	HPO:iea[2009-02-17]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0002928	PMID:15855260	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0000007	PMID:15855260	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0001249	OMIM:608782	IEA					P	HPO:iea[2009-02-17]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0003128	PMID:15855260	PCS	HP:0003623	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-13]
OMIM:608782	Pyruvate dehydrogenase phosphatase deficiency		HP:0003623	PMID:15855260	PCS		2/2			C	HPO:probinson[2023-05-13]
OMIM:226850	EPILEPSY-TELANGIECTASIA		HP:0001250	OMIM:226850	IEA					P	HPO:iea[2009-02-17]
OMIM:226850	EPILEPSY-TELANGIECTASIA		HP:0001939	OMIM:226850	IEA					P	HPO:iea[2009-02-17]
OMIM:226850	EPILEPSY-TELANGIECTASIA		HP:0001999	OMIM:226850	IEA					P	HPO:iea[2009-02-17]
OMIM:226850	EPILEPSY-TELANGIECTASIA		HP:0000007	OMIM:226850	IEA					I	HPO:iea[2009-02-17]
OMIM:226850	EPILEPSY-TELANGIECTASIA		HP:0000524	OMIM:226850	IEA					P	HPO:iea[2009-02-17]
OMIM:226850	EPILEPSY-TELANGIECTASIA		HP:0000664	OMIM:226850	IEA					P	HPO:iea[2009-02-17]
OMIM:226850	EPILEPSY-TELANGIECTASIA		HP:0001249	OMIM:226850	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0003577	OMIM:223900	IEA					C	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0003676	OMIM:223900	IEA					C	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001278	OMIM:223900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0012804	OMIM:223900	TAS					P	HPO:skoehler[2015-01-20]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:6000993	PMID:20301359	PCS					P	HPO:probinson[2024-08-03]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001252	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0002020	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001290	OMIM:223900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0012211	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0000712	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0008872	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001649	OMIM:223900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0005947	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0002019	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0000495	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0002014	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0002311	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001265	OMIM:223900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001069	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0002650	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0003387	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0002013	OMIM:223900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001063	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0004891	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0000096	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0008000	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0000822	OMIM:223900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0000007	PMID:11179008	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001954	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0000224	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0002821	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0001510	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0003138	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0003259	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:223900	Neuropathy, hereditary sensory and autonomic, type III		HP:0000522	OMIM:223900	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0008936	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0001298	PMID:10577905	PCS	HP:0003577	1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-12]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0000253	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0003577	PMID:10577905	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0002353	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0001250	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0001263	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0002063	OMIM:300673	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0002020	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0002093	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0001508	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0001419	PMID:10577905	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0007110	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0008872	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0002104	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0002126	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0001347	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:300673	Encephalopathy, neonatal severe, due to mecp2 mutations		HP:0001336	OMIM:300673	IEA					P	HPO:iea[2009-02-17]
OMIM:607499	Bulimia nervosa, susceptibility to, 1		HP:0001426	OMIM:607499	IEA					I	HPO:iea[2009-02-17]
OMIM:607499	Bulimia nervosa, susceptibility to, 1		HP:0100739	OMIM:607499	TAS					P	HPO:probinson[2012-07-22]
OMIM:310460	Myopia 1, X-linked		HP:0001419	OMIM:310460	TAS					I	HPO:skoehler[2012-11-20]
OMIM:310460	Myopia 1, X-linked		HP:0001417	OMIM:310460	IEA					I	HPO:iea[2009-02-17]
OMIM:310460	Myopia 1, X-linked		HP:0000545	OMIM:310460	IEA					P	HPO:iea[2009-02-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0002136	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0001123	OMIM:206570	IEA					P	HPO:iea[2009-02-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0002200	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0001250	OMIM:206570	IEA					P	HPO:iea[2009-02-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0002076	OMIM:206570	IEA					P	HPO:iea[2009-02-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0001260	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0001251	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0012444	OMIM:206570	TAS					P	HPO:skoehler[2013-11-28]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0012377	OMIM:206570	TAS					P	HPO:skoehler[2013-10-22]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0000726	OMIM:206570	IEA					P	HPO:iea[2009-02-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0000712	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0000965	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0000822	OMIM:206570	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0000007	OMIM:206570	IEA					I	HPO:iea[2009-02-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0007586	OMIM:206570	IEA					P	HPO:iea[2009-02-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0002977	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0002119	OMIM:206570	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206570	Angiomatosis, diffuse corticomeningeal, of divry and van bogaert		HP:0003745	OMIM:206570	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0032208	PMID:22870295	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0001166	PMID:22870295	PCS		1/1			P	HPO:skoehler[2014-08-24]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0000098	OMIM:615923	TAS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0010639	PMID:22870295	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0003577	PMID:22870295	PCS		1/1			C	HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0002650	PMID:22870295	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0031424	PMID:22870295	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0010055	PMID:22870295	PCS		1/1			P	HPO:skoehler[2014-08-24]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0000938	PMID:22870295	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0001847	PMID:22870295	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0002656	OMIM:615923	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0005769	PMID:22870295	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:615923	Epiphyseal chondrodysplasia, Miura type		HP:0000006	PMID:22870295	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-26]
OMIM:300115	Intellectual developmental disorder, X-linked 50		HP:0001417	OMIM:300115	IEA					I	HPO:skoehler[2013-01-11]
OMIM:601942	Diabetes mellitus, insulin-dependent, 10		HP:0000819	OMIM:601942	IEA					P	HPO:iea[2009-02-17]
OMIM:215518	Ciliary discoordination due to random ciliary orientation		HP:0002719	OMIM:215518	IEA					P	HPO:iea[2009-02-17]
OMIM:215518	Ciliary discoordination due to random ciliary orientation		HP:0001939	OMIM:215518	IEA					P	HPO:iea[2009-02-17]
OMIM:215518	Ciliary discoordination due to random ciliary orientation		HP:0000007	OMIM:215518	IEA					I	HPO:iea[2009-02-17]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0002079	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0001250	OMIM:615937	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0001162	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0000965	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0000238	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0002119	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0000256	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0007206	PMID:22497611;OMIM:615937	PCS		20/20			P	HPO:lccarmody[2018-10-25];HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0001249	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0002126	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0000974	OMIM:615937	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615937	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus syndrome 2		HP:0000006	OMIM:615937	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616580	Au-Kline syndrome		HP:0002465	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0003396	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0004442	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0003196	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001252	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0002020	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0012622	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0006191	OMIM:616580	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616580	Au-Kline syndrome		HP:0010297	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001845	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0002616	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000637	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000278	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0002019	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0000677	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0001249	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0001385	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0000494	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000175	OMIM:616580	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616580	Au-Kline syndrome		HP:0001344	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0002673	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0011968	PMID:26173930	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001263	PMID:26173930	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0012811	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0100259	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000407	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000767	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000689	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0002944	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0004209	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000960	PMID:26173930	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000006	PMID:26173930	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0005338	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000126	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000341	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0010946	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000540	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001195	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0030674	PMID:26173930	PCS		2/2			C	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0025480	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:4000105	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001508	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0008551	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0002119	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001869	OMIM:616580	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616580	Au-Kline syndrome		HP:0000218	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0002714	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0006610	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0002558	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001623	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000456	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0003422	PMID:26173930	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000076	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0025671	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001363	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0000430	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000474	PMID:26173930	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000276	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0005487	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000194	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000193	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0030001	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0003186	PMID:26173930	PCS		1/2			P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0000508	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0000426	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000822	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0001357	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000268	OMIM:616580	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616580	Au-Kline syndrome		HP:0000586	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0007018	PMID:26173930	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616580	Au-Kline syndrome		HP:0000028	PMID:26173930	PCS		2/2			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-02-18]
OMIM:620032	Ciliary dyskinesia, primary, 48, without situs inversus		HP:0012264	PMID:32185794	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620032	Ciliary dyskinesia, primary, 48, without situs inversus		HP:0001696	PMID:32185794	PCS		0/1			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620032	Ciliary dyskinesia, primary, 48, without situs inversus		HP:0002110	PMID:32185794	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620032	Ciliary dyskinesia, primary, 48, without situs inversus		HP:0000007	PMID:32185794	PCS					I	HPO:probinson[2022-10-03]
OMIM:620032	Ciliary dyskinesia, primary, 48, without situs inversus		HP:0000403	PMID:32185794	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620032	Ciliary dyskinesia, primary, 48, without situs inversus		HP:0006532	PMID:32185794	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:620032	Ciliary dyskinesia, primary, 48, without situs inversus		HP:0011108	PMID:32185794	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001012	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0003236	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002540	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000365	OMIM:617675	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001310	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000980	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0004322	OMIM:617675	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0003693	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000580	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001251	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001290	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001270	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000716	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000836	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000739	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002936	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000218	OMIM:617675	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001324	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0003326	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002058	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001265	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000750	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002078	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002650	OMIM:617675	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002750	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000870	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000276	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001288	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001761	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002075	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0002070	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0100753	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0100874	OMIM:617675	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000767	OMIM:617675	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000007	OMIM:617675	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001510	OMIM:617675	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000347	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000303	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000006	OMIM:617675	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0001337	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0000786	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617675	Myopathy, mitochondrial, and ataxia		HP:0003557	OMIM:617675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618546	Trichothiodystrophy 7, nonphotosensitive		HP:0000992	PMID:31374204	TAS		0/1			P	HPO:nvasilevsky[2019-09-11];HPO:nvasilevsky[2019-09-11];HPO:probinson[2024-03-15]
OMIM:618546	Trichothiodystrophy 7, nonphotosensitive		HP:0008064	PMID:31374204	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-15]
OMIM:618546	Trichothiodystrophy 7, nonphotosensitive		HP:0002299	PMID:31374204	PCS					P	HPO:nvasilevsky[2019-09-11];HPO:nvasilevsky[2019-09-11]
OMIM:618546	Trichothiodystrophy 7, nonphotosensitive		HP:0000007	PMID:31374204	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-15]
OMIM:618546	Trichothiodystrophy 7, nonphotosensitive		HP:0045055	PMID:31374204	PCS		2/2			P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2024-03-15]
OMIM:618546	Trichothiodystrophy 7, nonphotosensitive		HP:0007479	PMID:31374204	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:618546	Trichothiodystrophy 7, nonphotosensitive		HP:0007502	PMID:31374204	PCS					P	HPO:nvasilevsky[2019-09-11]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000286	PMID:34244665	PCS		2/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000340	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000582	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0003577	PMID:34244665	PCS					C	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000343	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000486	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0001250	PMID:34244665	PCS		10/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0002120	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0001252	PMID:34244665	PCS		10/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0003593	PMID:34244665	PCS					C	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0006150	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0012471	PMID:34244665	PCS		2/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0006055	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0001822	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0030084	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0009765	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0001249	PMID:34244665	PCS		18/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000577	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0003623	PMID:34244665	PCS					C	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000252	PMID:34244665	PCS		12/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000232	PMID:34244665	PCS		2/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000276	PMID:34244665	PCS		2/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0011304	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0011330	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000426	PMID:34244665	PCS		7/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0002705	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000268	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000664	PMID:34244665	PCS		3/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000565	PMID:34244665	PCS		2/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000322	PMID:34244665	PCS		2/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000006	PMID:34244665	PCS					I	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000369	PMID:34244665	PCS		1/19			P	HPO:probinson[2022-08-14]
OMIM:619880	Neurodevelopmental disorder with poor growth and skeletal anomalies		HP:0000303	PMID:34244665	PCS		2/19			P	HPO:probinson[2022-08-14]
OMIM:300854	Renal cell carcinoma, xp11-associated		HP:0001442	OMIM:300854	TAS					I	HPO:probinson[2013-02-20]
OMIM:300854	Renal cell carcinoma, xp11-associated		HP:0005584	OMIM:300854	TAS					P	HPO:probinson[2013-01-09]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0031956	PMID:30250217	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0003621	PMID:33075013	PCS		2/7			C	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0001396	PMID:33075013	PCS		7/7			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0000365	PMID:30250217	PCS		2/3			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0003155	PMID:30250217	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0001395	PMID:33075013	PCS		4/4			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0410053	PMID:33075013	PCS		0/7			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0003593	PMID:33075013;PMID:30250217	PCS		6/10			C	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0012852	PMID:33075013	PCS		1/4			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0031964	PMID:30250217	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0011463	PMID:33075013	PCS		1/7			C	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0000007	PMID:30250217	PCS					I	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0000989	PMID:30250217	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0002901	PMID:30250217	PCS		2/3			P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0001744	PMID:33075013	PCS		4/7			P	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0000952	PMID:33075013	PCS					P	HPO:probinson[2022-02-08]
OMIM:619658	Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss		HP:0003623	PMID:33075013	PCS		1/7			C	HPO:probinson[2022-02-08]
OMIM:180020	Retinal cone dystrophy 1		HP:0000551	OMIM:180020	TAS					P	HPO:probinson[2015-06-04]
OMIM:180020	Retinal cone dystrophy 1		HP:0000529	OMIM:180020	TAS					P	HPO:probinson[2009-02-17]
OMIM:180020	Retinal cone dystrophy 1		HP:0000613	OMIM:180020	TAS					P	HPO:probinson[2009-02-17]
OMIM:180020	Retinal cone dystrophy 1		HP:0000546	OMIM:180020	TAS					P	HPO:probinson[2009-02-17]
OMIM:180020	Retinal cone dystrophy 1		HP:0000548	OMIM:180020	IEA					P	HPO:skoehler[2015-12-30]
OMIM:180020	Retinal cone dystrophy 1		HP:0011504	OMIM:180020	TAS					P	HPO:probinson[2015-06-04]
OMIM:180020	Retinal cone dystrophy 1		HP:0000006	OMIM:180020	TAS					I	HPO:probinson[2009-02-17]
OMIM:180020	Retinal cone dystrophy 1		HP:0000512	OMIM:180020	TAS					P	HPO:probinson[2015-06-04]
OMIM:613375	Maturity-onset diabetes of the young, type 11		HP:0011462	PMID:19667185	PCS					C	HPO:probinson[2022-12-13]
OMIM:613375	Maturity-onset diabetes of the young, type 11		HP:0004904	PMID:19667185	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-12-13]
OMIM:613375	Maturity-onset diabetes of the young, type 11		HP:0025502	PMID:19667185	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-13]
OMIM:613375	Maturity-onset diabetes of the young, type 11		HP:0000006	PMID:19667185	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:613375	Maturity-onset diabetes of the young, type 11		HP:0001513	OMIM:613375	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001254	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0003145	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001332	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0002156	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0002497	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0003223	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001250	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0002120	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0003210	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001252	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001263	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0003593	OMIM:277410	IEA					C	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0002160	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001290	OMIM:277410	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0000639	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0012120	OMIM:277410	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001889	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0000007	OMIM:277410	IEA					I	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0002912	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0005518	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0003658	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0001249	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:277410	Methylmalonic aciduria and homocystinuria, Cbld type		HP:0003524	OMIM:277410	IEA					P	HPO:iea[2009-02-17]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0003202	PMID:24268661	PCS		4/4			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0003236	PMID:24268661	PCS		3/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0001055	PMID:24268661	PCS		2/8			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0003577	PMID:24268661	PCS		8/8			C	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0002650	PMID:24268661	PCS		2/8			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0001596	PMID:24268661	PCS		8/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0002164	PMID:24268661	PCS		1/8			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0002240	PMID:24268661	PCS		1/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0045075	PMID:24268661	PCS		8/8			P	HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0002091	PMID:24268661	PCS		5/5			P	HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0034392	PMID:24268661	PCS		5/6			P	HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0000518	PMID:24268661	PCS		1/8			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0000823	PMID:24268661	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0000966	PMID:24268661	PCS		7/7			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0001324	PMID:24268661	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0000653	PMID:24268661	PCS		4/8			P	HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0001510	PMID:24268661	PCS		2/8			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0002206	PMID:24268661	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0000006	PMID:24268661	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0001029	PMID:24268661	PCS	HP:0003577	8/8			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-02-18]
OMIM:615704	Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis		HP:0002522	PMID:24268661	PCS		3/3			P	HPO:probinson[2023-02-18]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0001276	OMIM:608033	IEA					P	HPO:iea[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0001298	PMID:19118815	PCS				HP:0033184	P	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-26]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0002510	OMIM:608033	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0001250	OMIM:608033	IEA					P	HPO:iea[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0003593	OMIM:608033	IEA					C	HPO:iea[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0002171	OMIM:608033	IEA					P	HPO:iea[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0002181	OMIM:608033	IEA					P	HPO:iea[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0002090	OMIM:608033	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0003829	OMIM:608033	TAS					I	HPO:skoehler[2012-10-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0002715	OMIM:608033	IEA					P	HPO:iea[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0002922	OMIM:608033	TAS					P	HPO:probinson[2009-02-17]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0000006	PMID:19118815	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0002445	OMIM:608033	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:608033	Encephalopathy, acute, infection-induced, susceptibility to, 3		HP:0001259	OMIM:608033	IEA					P	HPO:iea[2009-02-17]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0002069	PMID:23934111	PCS		3/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0002521	PMID:23934111	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0010819	PMID:23934111	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0001263	OMIM:617113	TAS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0003593	PMID:23934111	PCS		4/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0001251	OMIM:617113	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0001290	OMIM:617113	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0032794	PMID:23934111	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0100660	OMIM:617113	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0012469	PMID:23934111	PCS		3/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0100710	PMID:23934111	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0007270	PMID:23934111	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0200134	PMID:23934111	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0000752	OMIM:617113	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0007018	PMID:23934111	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0000006	PMID:23934111	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-02]
OMIM:617113	Epileptic encephalopathy, early infantile, 43		HP:0001249	PMID:23934111	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-02]
OMIM:618220	Retinitis pigmentosa 84		HP:0007737	PMID:24737827	PCS		1/1			P	HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0000662	PMID:24737827	PCS	HP:0011463	4/4			P	HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0000518	OMIM:618220	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618220	Retinitis pigmentosa 84		HP:0030553	PMID:24737827	PCS		4/4			P	HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0011463	PMID:24737827	PCS		4/4			C	HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0000007	PMID:24737827	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0007401	PMID:24737827	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0000510	PMID:24737827	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0007843	PMID:24737827	PCS		1/1			P	HPO:probinson[2023-01-18]
OMIM:618220	Retinitis pigmentosa 84		HP:0001116	PMID:24737827	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-18]
OMIM:616219	Fibrosis of extraocular muscles, congenital, 5		HP:0003577	PMID:25500261	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-30]
OMIM:616219	Fibrosis of extraocular muscles, congenital, 5		HP:0000508	PMID:25500261	PCS	HP:0003577	2/3			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-10-30]
OMIM:616219	Fibrosis of extraocular muscles, congenital, 5		HP:0000007	PMID:25500261	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-30]
OMIM:616219	Fibrosis of extraocular muscles, congenital, 5		HP:0009921	PMID:25500261	PCS	HP:0003577	1/3			P	HPO:probinson[2022-10-30]
OMIM:192430	Velocardiofacial syndrome		HP:0001155	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000220	PMID:1956057	PCS		38/38			P	HPO:iea[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0006549	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000023	PMID:1956057	PCS		3/38			P	HPO:iea[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0004322	PMID:1956057	PCS		24/38			P	HPO:iea[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000581	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0001252	PMID:1956057	PCS		29/38			P	HPO:skoehler[2010-06-20];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0011611	PMID:1956057	PCS	HP:0003577	2/16			P	HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0011999	OMIM:192430	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192430	Velocardiofacial syndrome		HP:0012841	OMIM:192430	TAS					P	HPO:skoehler[2014-11-26]
OMIM:192430	Velocardiofacial syndrome		HP:0002719	OMIM:192430	TAS					P	HPO:skoehler[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0001629	PMID:1956057	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000718	OMIM:192430	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000712	OMIM:192430	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192430	Velocardiofacial syndrome		HP:0001328	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000414	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0004935	PMID:1956057	PCS		2/16			P	HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000598	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000278	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0001249	PMID:1956057	PCS		31/38			P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000176	PMID:1956057	PCS		15/38			P	HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000175	PMID:1956057	PCS		7/38			P	HPO:iea[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000252	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0001883	PMID:1956057	PCS		4/38			P	HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000430	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000194	OMIM:192430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:192430	Velocardiofacial syndrome		HP:0045025	OMIM:192430	IEA					P	HPO:skoehler[2018-10-08]
OMIM:192430	Velocardiofacial syndrome		HP:0011840	PMID:1956057	PCS		2/38			P	HPO:skoehler[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000829	PMID:1956057	PCS		3/38			P	HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0011590	PMID:1956057	PCS	HP:0003577	1/16			P	HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000627	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0002627	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0001636	PMID:1956057	PCS		3/16			P	HPO:iea[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0001537	PMID:1956057	PCS		2/38			P	HPO:iea[2009-02-17];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0002901	PMID:1956057	PCS		5/38			P	HPO:skoehler[2010-06-20];HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0000201	OMIM:192430	TAS					P	HPO:skoehler[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000006	OMIM:192430	IEA					I	HPO:iea[2009-02-17]
OMIM:192430	Velocardiofacial syndrome		HP:0000028	PMID:1956057	IEA	HP:0003577	3/38			P	HP:probinson[2019-02-27]
OMIM:192430	Velocardiofacial syndrome		HP:0001611	OMIM:192430	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000286	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0008729	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0004322	PMID:16826520;PMID:25608830	PCS		10/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0001371	PMID:25608830	PCS		1/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000160	PMID:25608830	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0008807	PMID:25608830	PCS		1/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0009465	PMID:25608830	PCS		1/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0011461	PMID:16826520;PMID:25608830	PCS		14/14			C	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000316	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001884	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0200021	PMID:25608830	PCS		2/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0001488	PMID:25608830	PCS		1/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0001249	PMID:25608830	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000890	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000494	PMID:16826520	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000175	PMID:16826520	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0003083	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001060	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0012385	PMID:25608830	PCS		3/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0006380	PMID:25608830	PCS		3/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0002827	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0002828	PMID:25608830	PCS		2/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0002949	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001537	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000689	PMID:25608830	PCS		2/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000007	OMIM:265000	IEA					I	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0002944	PMID:25608830	PCS		1/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000207	PMID:25608830	PCS		1/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000405	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001059	PMID:16826520	PCS		11/11			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000047	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000369	PMID:25608830	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0002089	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000343	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000023	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0030319	PMID:16826520	PCS	HP:0003577	5/9			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0009760	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0009761	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001789	PMID:25608830	PCS		0/3			P	HPO:probinson[2022-06-24];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000218	PMID:16826520;PMID:25608830	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0002714	PMID:16826520	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0002557	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0004459	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000776	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001166	PMID:16826520	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0001762	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0002650	PMID:16826520;PMID:25608830	PCS		8/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000276	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001288	PMID:25608830	PCS		1/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000470	PMID:25608830	PCS		2/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0001838	PMID:16826520;PMID:25608830	PCS		12/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24];HPO:probinson[2022-06-24];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000902	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0002808	PMID:16826520	PCS		7/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0009110	OMIM:265000	TAS					P	HPO:probinson[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000508	PMID:16826520	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0001558	PMID:16826520	PCS	HP:0011461	6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0001558	PMID:25608830	PCS		3/3			P	HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0002804	PMID:16826520	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0006443	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001836	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0001159	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0009757	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0009756	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0006446	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0002643	PMID:16826520	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0009759	OMIM:265000	IEA					P	HPO:iea[2009-02-17]
OMIM:265000	Escobar syndrome		HP:0000347	PMID:25608830	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:265000	Escobar syndrome		HP:0000028	PMID:16826520	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-24]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0004325	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0002421	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0003577	OMIM:608027	IEA					C	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0003676	OMIM:608027	IEA					C	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000365	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000343	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0002365	OMIM:608027	TAS					P	HPO:skoehler[2014-04-04]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0004322	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0001272	PMID:25832664	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0001250	PMID:25832664	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0003593	PMID:25832664	PCS		4/4			C	HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0012110	PMID:25832664;OMIM:608027	PCS		11/11			P	HPO:skoehler[2014-04-22];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0007366	PMID:25832664	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000637	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0002714	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000218	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0001347	PMID:25832664	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0008936	PMID:25832664	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000253	OMIM:608027	IEA					P	HPO:skoehler[2015-01-21]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0002059	PMID:25832664	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0001321	OMIM:608027	TAS					P	HPO:skoehler[2014-04-22]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0002079	PMID:25832664	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000293	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0001263	PMID:25832664	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0005280	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0034295	PMID:25832664	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000007	PMID:25832664	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0002705	OMIM:608027	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0001319	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000648	PMID:25832664	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000400	OMIM:608027	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000543	PMID:25832664	PCS		1/4			P	HPO:probinson[2023-02-19]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000520	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0001257	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000248	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:608027	Pontocerebellar hypoplasia, type 3		HP:0000369	OMIM:608027	IEA					P	HPO:iea[2009-02-17]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000286	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0003577	PMID:26660953	PCS		1/1			C	HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001176	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000486	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0410255	PMID:26660953	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0030037	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000023	PMID:26660953	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000480	PMID:26660953	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0010741	PMID:26660953	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001629	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0012471	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0002619	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0002979	OMIM:617107	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000316	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001548	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001847	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000637	PMID:26660953	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000158	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000411	PMID:26660953	PCS		1/1			P	HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000256	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001763	OMIM:617107	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000311	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0004712	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000110	OMIM:617107	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000494	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000098	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001520	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000490	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001263	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0011800	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000407	OMIM:617107	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000107	OMIM:617107	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000007	PMID:26660953	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-06]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001833	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000400	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0002667	OMIM:617107	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0000589	OMIM:617107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617107	Thauvin-Robinet-Faivre syndrome		HP:0001634	OMIM:617107	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003037	OMIM:184252	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003015	OMIM:184252	TAS					P	HPO:skoehler[2012-10-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001498	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003311	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003375	PMID:19232556	PCS		4/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003593	PMID:19232556	PCS		1/6			C	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0011463	PMID:19232556	PCS		3/6			C	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0010230	PMID:19232556	PCS		0/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0006375	PMID:19232556	PCS		0/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001547	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002812	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002515	PMID:19232556	PCS		2/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0008833	OMIM:184252	TAS					P	HPO:probinson[2012-05-26]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002657	PMID:19232556	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001760	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003521	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002751	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003621	PMID:19232556	PCS		2/6			C	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002650	PMID:19232556	PCS	HP:0003577	3/5			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002750	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000470	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0005042	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0005041	PMID:19232556	PCS		5/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0005280	PMID:19232556	PCS		2/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003180	PMID:19232556	PCS		4/6			P	HPO:probinson[2012-05-26];HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000926	PMID:19232556	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002869	PMID:19232556	PCS		5/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000348	PMID:19232556	PCS		2/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002826	PMID:19232556	PCS		4/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000768	OMIM:184252	IEA					P	HPO:iea[2009-02-17]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002987	PMID:19232556	PCS		1/6			P	HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000006	PMID:19232556	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:184252	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001216	PMID:19232556	PCS		4/4		HP:0012828	P	HPO:probinson[2022-03-16]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001298	OMIM:618234	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0002650	OMIM:618234	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0003198	OMIM:618234	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001263	PMID:17557076	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0002151	OMIM:618234	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001252	PMID:17557076	PCS		1/1			P	HPO:probinson[2023-03-19]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0002240	OMIM:618234	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0003593	PMID:17557076	PCS		1/1			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-19]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0000580	PMID:17557076	PCS		1/1			P	HPO:probinson[2023-03-19]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0011923	PMID:17557076	PCS		1/1			P	HPO:probinson[2023-03-19]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0000939	OMIM:618234	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001508	PMID:17557076	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001639	PMID:17557076	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0002808	OMIM:618234	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0100704	PMID:17557076	PCS		1/1			P	HPO:probinson[2023-03-19]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001716	PMID:17557076	PCS		1/1			P	HPO:probinson[2023-03-19]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0000007	PMID:17557076	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-19]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001635	PMID:17557076	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001403	OMIM:618234	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0001942	OMIM:618234	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618234	Mitochondrial complex I deficiency, nuclear type 11		HP:0003128	PMID:17557076	PCS		1/1			P	HPO:probinson[2023-03-19]
OMIM:615710	Mitchell-Riley syndrome		HP:0002014	OMIM:615710	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615710	Mitchell-Riley syndrome		HP:0002245	PMID:26264437	PCS		1/10			P	HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0001396	PMID:26264437	PCS		7/10			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0003577	PMID:26264437	PCS		9/10			C	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0001541	PMID:26264437	PCS		1/10			P	HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0005235	OMIM:615710	TAS		4/10			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0002024	PMID:26264437	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0002594	PMID:26264437	PCS		2/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0011467	PMID:26264437	PCS		8/10			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0003074	OMIM:615710	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615710	Mitchell-Riley syndrome		HP:0011985	OMIM:615710	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615710	Mitchell-Riley syndrome		HP:0000819	PMID:26264437	PCS		10/10			P	HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0002904	OMIM:615710	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615710	Mitchell-Riley syndrome		HP:0001734	PMID:26264437	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0000007	PMID:20148032	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0001511	OMIM:615710	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615710	Mitchell-Riley syndrome		HP:0005912	OMIM:615710	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615710	Mitchell-Riley syndrome		HP:0002247	PMID:26264437	PCS		9/10			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0002566	PMID:26264437	PCS		5/10			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:615710	Mitchell-Riley syndrome		HP:0001545	PMID:26264437	PCS		1/10			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-02-12]
OMIM:261500	Eosinophil peroxidase deficiency		HP:0034253	PMID:7809065	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:261500	Eosinophil peroxidase deficiency		HP:0000007	PMID:7809065	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:216950	Complement component c1r deficiency		HP:0002960	OMIM:216950	IEA					P	HPO:iea[2009-02-17]
OMIM:216950	Complement component c1r deficiency		HP:0007417	OMIM:216950	IEA					P	HPO:iea[2009-02-17]
OMIM:216950	Complement component c1r deficiency		HP:0000123	OMIM:216950	TAS				HP:0012825	P	HPO:skoehler[2010-06-20]
OMIM:216950	Complement component c1r deficiency		HP:0004431	OMIM:216950	IEA					P	HPO:iea[2009-02-17]
OMIM:216950	Complement component c1r deficiency		HP:0002829	OMIM:216950	IEA					P	HPO:iea[2009-02-17]
OMIM:216950	Complement component c1r deficiency		HP:0000007	OMIM:216950	IEA					I	HPO:iea[2009-02-17]
OMIM:216950	Complement component c1r deficiency		HP:0002837	OMIM:216950	TAS					P	HPO:probinson[2009-02-17]
OMIM:216950	Complement component c1r deficiency		HP:0001369	OMIM:216950	TAS					P	HPO:probinson[2009-02-17]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0003422	PMID:28792876	PCS		2/2			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000252	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0003577	PMID:28792876	PCS		2/2			C	HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000750	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0008905	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0001883	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000089	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0004322	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000122	PMID:28792876	PCS		1/2			P	HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0004383	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:6000776	PMID:28792876	PCS		3/3			P	HPO:probinson[2024-06-29]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0005280	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0012622	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0002937	PMID:28792876	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000007	PMID:28792876	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000878	PMID:28792876	PCS		1/2			P	HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0002007	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000774	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0001643	PMID:28792876	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0000369	PMID:28792876	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-23]
OMIM:617661	Vertebral, cardiac, renal, and limb defects syndrome 2		HP:0001545	PMID:28792876	PCS		1/2			P	HPO:probinson[2022-08-23]
OMIM:601003	Brody myopathy		HP:0002047	PMID:23911890	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0002411	PMID:10914677	PCS		0/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0031826	PMID:8841193	PCS		0/5			P	HPO:probinson[2019-11-28];HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0002486	PMID:10914677	PCS		0/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0001371	PMID:10914677	PCS		0/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0003474	PMID:8841193	PCS		0/5			P	HPO:probinson[2019-11-28];HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0100284	PMID:8841193	PCS		0/5			P	HPO:probinson[2019-11-28];HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0002380	PMID:10914677	PCS		0/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0001270	PMID:23911890	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0010548	PMID:10914677;PMID:8841193	PCS		0/10			P	HP:probinson[2022-03-07];HPO:probinson[2019-11-28];HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0011463	PMID:10914677	PCS		5/5			C	HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0009046	PMID:10914677	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0000007	PMID:8841193	PCS					I	HPO:probinson[2012-07-28];HPO:probinson[2019-11-28]
OMIM:601003	Brody myopathy		HP:0001324	PMID:10914677	PCS		0/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0003712	PMID:10914677	PCS		0/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0008967	PMID:10914677;PMID:8841193	PCS		10/10			P	HP:probinson[2022-03-07];HPO:probinson[2019-11-28];HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0003710	PMID:23911890	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0003326	PMID:10914677	PCS		0/5			P	HP:probinson[2022-03-07]
OMIM:601003	Brody myopathy		HP:0003623	PMID:23911890	PCS		1/1			C	HPO:probinson[2022-03-07]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0003577	PMID:11687798	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0003113	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0005576	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0000083	OMIM:602522	TAS					P	HPO:probinson[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001252	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001290	OMIM:602522	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001270	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0012605	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001508	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0000859	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001789	OMIM:602522	TAS					P	HPO:probinson[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0002914	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0004737	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001249	OMIM:602522	IEA					P	HPO:skoehler[2010-06-18]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001622	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001265	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001561	OMIM:602522	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001563	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0005565	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0012213	OMIM:602522	TAS					P	HPO:skoehler[2013-03-15]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0003081	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0000969	OMIM:602522	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0004909	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0001959	PMID:12574213	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0000407	PMID:11687798	PCS	HP:0003577	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0002902	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0000007	PMID:11687798	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-03]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0002900	PMID:12574213	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0004727	PMID:12574213	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0000103	PMID:11687798	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:602522	Bartter syndrome, type 4A, neonatal, with sensorineural deafness		HP:0000127	OMIM:602522	IEA					P	HPO:iea[2009-02-17]
OMIM:612731	Faciocardiomelic syndrome		HP:0000154	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0000252	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0000343	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0008839	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0001520	OMIM:612731	TAS					P	HPO:skoehler[2013-01-22]
OMIM:612731	Faciocardiomelic syndrome		HP:0000463	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0003100	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0010764	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0011565	OMIM:612731	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612731	Faciocardiomelic syndrome		HP:0010442	OMIM:612731	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612731	Faciocardiomelic syndrome		HP:0005280	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0000506	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0000938	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0000508	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0000007	OMIM:612731	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0000689	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0430028	OMIM:612731	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612731	Faciocardiomelic syndrome		HP:0000774	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0200000	OMIM:612731	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612731	Faciocardiomelic syndrome		HP:0000347	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0001249	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0002753	OMIM:612731	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612731	Faciocardiomelic syndrome		HP:0000577	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612731	Faciocardiomelic syndrome		HP:0004634	OMIM:612731	IEA					P	HPO:skoehler[2010-06-19]
OMIM:270425	Sodium-Potassium-Atpase activity of red cell		HP:0001939	OMIM:270425	IEA					P	HPO:iea[2009-02-17]
OMIM:270425	Sodium-Potassium-Atpase activity of red cell		HP:0000007	OMIM:270425	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0000252	PMID:21937992	PCS		4/4			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0001344	PMID:23773660	PCS		2/2			P	HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0001263	PMID:23773660	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0001252	PMID:23773660	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0003593	PMID:23773660	PCS		2/2			C	HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0011800	PMID:23773660	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0005280	PMID:23773660	PCS		1/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0032988	PMID:23773660	PCS		1/2			P	HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0001508	PMID:23773660	PCS		1/2			P	HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0000718	PMID:23773660	PCS		1/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0000007	PMID:21937992	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0001510	PMID:23773660	PCS		1/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-02-24]
OMIM:614340	Intellectual developmental disorder, autosomal recessive 27		HP:0001249	PMID:21937992	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-02-24]
OMIM:600335	Succinic acidemia		HP:0002098	OMIM:600335	IEA					P	HPO:iea[2009-02-17]
OMIM:600335	Succinic acidemia		HP:0000007	OMIM:600335	IEA					I	HPO:iea[2009-02-17]
OMIM:600335	Succinic acidemia		HP:0003128	OMIM:600335	IEA					P	HPO:iea[2009-02-17]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001298	PMID:24259288	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002267	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0004446	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002266	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0004322	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001051	OMIM:300868	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003593	PMID:24259288;PMID:29502866;PMID:24357517	PCS		10/10			C	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012745	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0031145	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000081	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0006191	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000637	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0006994	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002139	PMID:22305531	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001169	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003487	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003121	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012736	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001182	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002705	PMID:25885527;PMID:22305531	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0006986	OMIM:300868	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001397	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003577	PMID:25885527;PMID:22305531	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001399	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002123	PMID:25885527;PMID:22305531;PMID:24706016;PMID:29502866;PMID:24357517	PCS		8/8			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000980	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001272	PMID:24357517	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002120	PMID:24259288;PMID:24357517	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2014-06-24];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001394	OMIM:300868	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002240	PMID:24259288;PMID:25885527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001270	PMID:22305531;PMID:24357517	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0030515	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0100704	PMID:24259288	PCS		3/3			P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002119	PMID:24259288;PMID:24259184	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0025116	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0005989	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002236	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002599	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0006956	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000076	PMID:22305531;PMID:24706016	PCS		4/5			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002133	PMID:29502866;PMID:24357517	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002376	PMID:24259184;PMID:29502866	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0004673	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002373	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0007370	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001712	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0004308	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000288	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001371	PMID:24259288;PMID:22305531;PMID:24706016	PCS		7/7			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001250	PMID:24259288;PMID:24706016;PMID:24357517	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000160	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001252	PMID:22305531;PMID:29502866	PCS		3/3			P	HPO:skoehler[2012-10-16];HPO:probinson[2024-07-30];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000280	PMID:24259288	PCS		1/1			P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012704	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0007361	OMIM:300868	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000717	PMID:24706016	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003429	PMID:24706016	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001367	PMID:24706016	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001488	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003202	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000054	OMIM:300868	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001263	PMID:9307258;PMID:24259184;PMID:24357517	PCS		16/16		HP:0012828	P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:nvasilevsky[2019-03-27]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0011168	PMID:29502866	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012385	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0009890	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0006380	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000969	PMID:24357517	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001257	PMID:24259288	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002104	PMID:25885527;PMID:24259184;PMID:22305531	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0011951	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0011952	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0009085	PMID:24259288;PMID:24259184	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000817	PMID:29502866	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001103	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000256	OMIM:300868	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001348	PMID:24259288;PMID:22305531	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003765	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001347	PMID:24706016	PCS		3/3			P	HPO:skoehler[2012-10-16];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000396	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001000	OMIM:300868	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000271	PMID:24706016	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0011947	PMID:24357517	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000272	PMID:22305531;PMID:24357517	PCS		1/3			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0010851	PMID:24706016	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0040130	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0005280	PMID:22305531;PMID:24357517;PMID:29502866	PCS		3/5			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012001	PMID:29502866	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000029	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001357	PMID:24259288;PMID:25885527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002445	PMID:24706016	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000269	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001331	PMID:22305531	PCS		1/1			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002421	PMID:29502866	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000365	PMID:24259288;PMID:25885527	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002540	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001695	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001332	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0005257	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012103	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012469	PMID:25885527;PMID:24357517	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0040134	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000239	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000252	OMIM:300868	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001341	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001344	PMID:24259288	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000496	PMID:24259288	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0030903	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0011129	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012465	PMID:24259288	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0100538	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0025404	PMID:29502866	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000007	PMID:24357517	PCS					I	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003517	OMIM:300868	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0200034	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000248	PMID:24259288;PMID:25885527	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0006349	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000126	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001336	PMID:24259288;PMID:24706016;PMID:24357517	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002521	PMID:25885527;PMID:24706016;PMID:24357517	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2014-06-24];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001792	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:nvasilevsky[2019-03-27];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000582	PMID:24259184;PMID:22305531	PCS		2/3			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000463	PMID:22305531;PMID:29502866	PCS		3/4			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012448	OMIM:300868	TAS					P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001548	OMIM:300868	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000337	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001789	PMID:8599356	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002878	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000218	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000212	PMID:22305531	PCS		1/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001667	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002753	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001561	PMID:24259184;PMID:22305531;PMID:24706016	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2017-07-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002650	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000233	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001321	PMID:22305531	PCS		2/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000474	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0010818	PMID:24706016	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0005484	PMID:24259288;PMID:25885527	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000470	PMID:22305531	PCS		1/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002090	PMID:22305531;PMID:24357517	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0008064	OMIM:300868	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002529	PMID:24259288	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0200134	PMID:24259184;PMID:22305531	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2014-06-24];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001433	PMID:24259288	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000347	OMIM:300868	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002069	PMID:24357517;PMID:29502866	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000684	PMID:24259288	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003155	PMID:25885527;PMID:24259184;PMID:22305531;PMID:24706016	PCS		7/8			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003273	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002063	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002061	OMIM:300868	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003270	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012429	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0012430	PMID:24706016	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0009381	PMID:22305531	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0011461	PMID:22305531	PCS		2/2			C	HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000316	PMID:25885527;PMID:29502866	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2017-07-13];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001522	PMID:22305531	PCS		2/2			C	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001643	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000674	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000311	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000556	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003700	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0005469	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002510	PMID:24706016	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002078	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001541	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002079	PMID:24259184;PMID:22305531;PMID:24706016	PCS		9/9			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002197	PMID:24259184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000691	PMID:24259288	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0040194	OMIM:300868	TAS					P	HPO:nvasilevsky[2019-03-27]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0003281	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0007190	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001419	PMID:22305531	PCS					I	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0011330	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000207	OMIM:300868	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002987	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000201	PMID:22305531;PMID:24357517	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002500	PMID:24357517	PCS		1/1			P	HPO:skoehler[2012-10-16];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001414	PMID:22305531	PCS		1/2			P	HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000324	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001413	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000687	PMID:24259288	PCS		1/1			P	HPO:skoehler[2014-06-24]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002835	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002714	PMID:22305531;PMID:24357517	PCS		1/3			P	HPO:skoehler[2012-10-16];HPO:probinson[2022-08-13];ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001623	PMID:22305531;PMID:24357517	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:probinson[2022-08-13];HPO:probinson[2022-08-13]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001744	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001760	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0008936	PMID:24259288;PMID:25885527;PMID:24259184;PMID:22305531;PMID:24357517	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2014-06-24];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002179	PMID:29502866	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002059	PMID:25885527;PMID:24259184	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002056	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001520	PMID:25885527	PCS		1/1			P	HPO:skoehler[2012-10-16];HPO:probinson[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002174	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0009909	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0002171	PMID:24259288	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000543	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001631	PMID:24259184;PMID:22305531	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-30];HPO:skoehler[2012-10-16];HPO:nvasilevsky[2019-03-27];HPO:probinson[2019-07-03]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0001873	PMID:24259288	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2		HP:0000545	PMID:25885527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-30]
OMIM:606744	Seckel syndrome 2		HP:0000341	PMID:21998596	PCS					P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0002135	PMID:24389050	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:606744	Seckel syndrome 2		HP:0000252	PMID:21998596	PCS					P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0007429	PMID:21998596	PCS					P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0003577	PMID:24389050	PCS		1/1			C	HPO:probinson[2024-03-10]
OMIM:606744	Seckel syndrome 2		HP:0030148	OMIM:606744	TAS					P	HPO:skoehler[2014-11-26]
OMIM:606744	Seckel syndrome 2		HP:0004322	PMID:24389050	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-10]
OMIM:606744	Seckel syndrome 2		HP:0001321	PMID:11781686	PCS					P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0000171	PMID:24389050	PCS		1/1			P	HPO:skoehler[2014-06-24]
OMIM:606744	Seckel syndrome 2		HP:0000691	PMID:24389050	PCS		1/1			P	HPO:skoehler[2014-06-24]
OMIM:606744	Seckel syndrome 2		HP:0000086	OMIM:606744	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:606744	Seckel syndrome 2		HP:0001518	PMID:24389050	PCS		1/1			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-03-10]
OMIM:606744	Seckel syndrome 2		HP:0011342	PMID:21998596	PCS					P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0011451	PMID:24389050	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:606744	Seckel syndrome 2		HP:0007352	PMID:24389050	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:606744	Seckel syndrome 2		HP:0000448	PMID:21998596	PCS					P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0000568	PMID:24389050	PCS		1/1			P	HPO:skoehler[2014-06-24]
OMIM:606744	Seckel syndrome 2		HP:0000007	PMID:21998596	PCS					I	HPO:probinson[2013-01-09]
OMIM:606744	Seckel syndrome 2		HP:0004209	PMID:21998596	PCS					P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0000047	PMID:11781686	PCS				HP:0012825	P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0001620	PMID:11781686	PCS		4/4		HP:0012825	P	HPO:probinson[2013-02-24]
OMIM:606744	Seckel syndrome 2		HP:0001510	PMID:21998596;PMID:24389050	PCS		11/11			P	HPO:probinson[2013-02-24];HPO:probinson[2024-03-10]
OMIM:606744	Seckel syndrome 2		HP:0000347	PMID:24389050	PCS		1/1			P	HPO:skoehler[2014-06-24]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0004325	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002421	PMID:25981959;PMID:37821226;PMID:27062503;PMID:25794864	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000640	PMID:22986007	PCS		2/4			P	HP:probinson[2022-03-14];HPO:probinson[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002540	PMID:37964426;PMID:35743164;PMID:22986007	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003596	PMID:22986007	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000486	PMID:29925855;PMID:37964426	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001332	PMID:37821226;PMID:29925855	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000089	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0004322	PMID:37821226;PMID:37964426	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002384	PMID:22986007	PCS		2/4			P	HP:probinson[2022-03-14];HPO:probinson[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0030177	PMID:29925855	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003593	PMID:25981959;PMID:29925855;PMID:37964426;PMID:28620721;PMID:27062503;PMID:22986007;PMID:25794864	PCS		11/29			C	ORCID:0000-0002-0736-9199[2024-07-17];HPO:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001290	PMID:37821226;PMID:27062503;PMID:25794864	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000639	PMID:37821226;PMID:29925855;PMID:37964426;PMID:28488678;PMID:28620721;PMID:27062503;PMID:28826917;PMID:15623688;PMID:22986007;PMID:35743164;PMID:25794864	PCS		32/43			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000514	PMID:28826917	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003763	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000252	PMID:37821226;PMID:37964426	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001583	PMID:25981959	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0004691	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0100021	PMID:25981959;PMID:37821226;PMID:29925855;PMID:37964426;PMID:28488678;PMID:28620721;PMID:27062503;PMID:28826917;PMID:35743164;PMID:22986007;PMID:25794864	PCS		4/48			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0011094	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000805	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000526	PMID:29925855;PMID:37964426	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002307	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007676	PMID:29925855;PMID:28488678	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000006	PMID:15623688	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002423	PMID:25981959	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001337	PMID:37964426;PMID:28620721;PMID:35743164	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001336	PMID:29925855;PMID:28826917	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001276	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003577	PMID:37964426;PMID:28488678;PMID:27062503;PMID:28826917;PMID:15623688;PMID:25794864	PCS		26/32			C	HPO:iea[2009-02-17];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003698	PMID:25794864	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000582	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002002	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001310	PMID:37821226;PMID:37964426;PMID:28488678;PMID:28620721;PMID:15623688	PCS		24/26			P	HPO:skoehler[2013-02-25];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001272	PMID:29925855;PMID:37964426;PMID:28488678;PMID:27062503;PMID:35743164;PMID:22986007;PMID:25794864	PCS		21/25			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002120	PMID:29925855	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001270	PMID:15623688;PMID:35743164;PMID:22986007	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0034435	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002080	PMID:37964426;PMID:15623688;PMID:22986007	PCS		13/16			P	HPO:skoehler[2013-02-25];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0100275	PMID:37964426;PMID:22986007;PMID:35743164	PCS		3/14			P	ORCID:0000-0002-0736-9199[2024-07-17];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0100543	PMID:37821226;PMID:29925855	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000617	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0100704	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000616	PMID:28620721	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0100702	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0009049	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000218	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0006855	PMID:29925855;PMID:28826917;PMID:15623688;PMID:22986007	PCS		9/15			P	HP:probinson[2022-03-14];HPO:probinson[2024-07-17];HPO:iea[2009-02-17];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001320	PMID:15623688	PCS		2/5			P	HPO:probinson[2021-10-23]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002136	PMID:37821226;PMID:28826917	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-07-17];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002015	PMID:37821226;PMID:27062503;PMID:25794864	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002411	PMID:37821226;PMID:28826917	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000750	PMID:37821226;PMID:37964426;PMID:22986007	PCS		7/9			P	HP:probinson[2022-03-14];HPO:probinson[2024-07-17];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001321	PMID:37964426	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002376	PMID:25981959	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001288	PMID:37964426	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000474	PMID:25981959	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0004396	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0005484	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000508	PMID:37821226;PMID:37964426	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0009830	PMID:27062503;PMID:25794864	PCS		0/8			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007256	PMID:27062503;PMID:28826917;PMID:25794864	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001319	PMID:37964426;PMID:27062503	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002406	PMID:22986007	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0004428	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002007	PMID:37821226	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002403	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0004425	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002465	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002345	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0010529	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003676	PMID:28488678;PMID:35743164	PCS		2/10			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001256	PMID:37964426;PMID:28488678;PMID:15623688;PMID:35743164;PMID:25794864	PCS		23/23			P	HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002342	PMID:25981959;PMID:37964426;PMID:35743164;PMID:25794864	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000563	PMID:28620721	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0031629	PMID:37821226;PMID:37964426;PMID:15623688	PCS		11/11			P	HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001250	PMID:29925855;PMID:27062503;PMID:25794864	PCS		0/13			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002066	PMID:15623688;PMID:22986007	PCS		6/13			P	HPO:probinson[2021-10-23];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001252	PMID:25981959;PMID:29925855;PMID:37964426;PMID:28620721;PMID:28826917;PMID:22986007;PMID:35743164	PCS		23/26			P	HP:probinson[2022-03-14];HPO:probinson[2024-07-17];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001251	PMID:25981959;PMID:29925855;PMID:37964426;PMID:28620721;PMID:27062503;PMID:28826917;PMID:35743164;PMID:25794864	PCS		30/30			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0012428	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003391	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0033128	PMID:25981959;PMID:28826917	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0011463	PMID:29925855;PMID:28620721;PMID:28826917	PCS		9/12			C	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007366	PMID:27062503;PMID:25794864	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0020045	PMID:29925855;PMID:37964426	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0025336	PMID:25981959;PMID:37964426;PMID:28620721;PMID:27062503;PMID:22986007;PMID:25794864	PCS		16/16			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007885	PMID:29925855;PMID:37964426	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007369	PMID:27062503	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0003701	PMID:37964426;PMID:22986007	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0020049	PMID:29925855	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001642	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001249	PMID:37821226;PMID:27062503;PMID:28826917;PMID:35743164	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000555	PMID:37821226	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002078	PMID:28488678	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0030147	PMID:22986007	PCS		2/4			P	HP:probinson[2022-03-14];HPO:probinson[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0025335	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0011968	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0006817	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001260	PMID:37821226;PMID:37964426;PMID:28488678;PMID:28620721;PMID:28826917;PMID:15623688;PMID:22986007;PMID:35743164	PCS		24/31			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000570	PMID:28620721	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001263	PMID:37964426;PMID:27062503;PMID:22986007;PMID:35743164	PCS		9/11			P	ORCID:0000-0002-0736-9199[2024-07-17];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002470	PMID:37821226;PMID:15623688	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002075	PMID:15623688	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-23]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0033257	PMID:25981959;PMID:28826917;PMID:22986007;PMID:25794864	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002194	PMID:22986007	PCS		1/4			P	HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002070	PMID:28826917;PMID:15623688;PMID:22986007	PCS		6/15			P	HPO:skoehler[2013-02-25];HPO:probinson[2021-10-23];ORCID:0000-0002-0736-9199[2024-07-17];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002071	PMID:28488678;PMID:27062503;PMID:25794864	PCS		6/14			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0012896	PMID:29925855	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000448	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002505	PMID:28826917	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000565	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002346	PMID:28488678	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002169	PMID:28488678	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007979	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007859	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002442	PMID:29925855;PMID:37964426	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000540	PMID:37964426	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0430025	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001350	PMID:27062503;PMID:35743164;PMID:25794864	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0010862	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0031491	PMID:22986007	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0007340	PMID:37964426;PMID:22986007	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000657	PMID:29925855;PMID:28620721;PMID:27062503;PMID:35743164;PMID:25794864	PCS		10/20			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001627	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001348	PMID:25981959	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001347	PMID:37821226;PMID:28488678;PMID:22986007	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002179	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002059	PMID:29925855	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0008935	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0031936	PMID:25981959;PMID:37821226;PMID:37964426;PMID:27062503;PMID:28826917;PMID:22986007	PCS		12/14			P	ORCID:0000-0002-0736-9199[2024-07-17];HP:probinson[2022-03-14]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0002174	PMID:28488678;PMID:27062503;PMID:28826917;PMID:25794864	PCS		15/16			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0032988	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001518	PMID:37821226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0033683	PMID:37821226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001999	PMID:35743164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0009878	PMID:37964426;PMID:28488678	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0001631	PMID:28620721	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000028	PMID:35743164	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:117360	Spinocerebellar ataxia 29, congenital nonprogressive		HP:0000666	PMID:37964426	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:619102	Spermatogenic failure 47		HP:0003251	PMID:32051257	PCS		2/2			P	HPO:probinson[2020-12-10]
OMIM:619102	Spermatogenic failure 47		HP:0000007	PMID:32051257	PCS					I	HPO:probinson[2020-12-10];HPO:probinson[2020-12-10]
OMIM:619102	Spermatogenic failure 47		HP:0012208	PMID:32051257	PCS		2/2			P	HPO:probinson[2020-12-10]
OMIM:619102	Spermatogenic failure 47		HP:0032558	PMID:32051257	PCS		2/2			P	HPO:probinson[2020-12-10]
OMIM:619102	Spermatogenic failure 47		HP:0000798	PMID:32051257	PCS		2/2			P	HPO:probinson[2020-12-10]
OMIM:619102	Spermatogenic failure 47		HP:0032559	PMID:32051257	PCS		2/2			P	HPO:probinson[2020-12-10]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0003236	PMID:26136523	PCS		8/10			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-22]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0003388	OMIM:616231	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0003394	PMID:26136523	PCS		4/10			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-22]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0034940	PMID:30258016	PCS		2/2			P	HPO:probinson[2023-07-18]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0001324	PMID:26136523	PCS		1/10		HP:0012840	P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-22]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0003701	OMIM:616231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0000006	PMID:26136523	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-22]
OMIM:616231	Myopathy, vacuolar, with CASQ1 aggregates		HP:0003326	PMID:26136523	PCS		3/10			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-22]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0001265	OMIM:609311	IEA					P	HPO:iea[2009-02-17]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0033748	PMID:15744041	PCS		6/6			P	HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0003431	PMID:15744041	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0002650	PMID:15744041	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0001762	PMID:15744041	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0001245	PMID:15744041	PCS		2/6			P	HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0001761	PMID:15744041	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0003484	OMIM:609311	IEA					P	HPO:probinson[2012-03-13]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0003383	PMID:15744041	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0001284	PMID:15744041	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0001270	PMID:15744041	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0010487	PMID:15744041	PCS		2/6			P	HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0003380	PMID:15744041	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0007182	PMID:15744041	PCS					P	HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0009053	PMID:15744041	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0011463	PMID:15744041	PCS		6/6			C	HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0000007	PMID:17564959	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0002936	PMID:15744041	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0002515	PMID:15744041	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0002317	PMID:15744041	PCS		6/6			P	HPO:probinson[2021-06-26]
OMIM:609311	Charcot-marie-tooth disease, type 4H		HP:0008944	PMID:15744041	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0002015	PMID:38423010	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0006989	PMID:38423010	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0003577	PMID:38423010	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0002353	PMID:38423010	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0002376	PMID:38423010	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0002079	PMID:38423010	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0001250	PMID:38423010	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0011968	PMID:38423010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0001272	PMID:38423010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0002352	PMID:38423010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0001263	PMID:38423010	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0002283	PMID:38423010	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0001274	PMID:38423010	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0001252	PMID:38423010	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0033454	PMID:38423010	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0000609	PMID:38423010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0000639	PMID:38423010	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0000649	PMID:38423010	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0008278	PMID:38423010	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0001302	PMID:38423010	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0001249	PMID:38423010	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620783	Developmental and epileptic encephalopathy 115		HP:0000006	PMID:38423010	PCS					I	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:614432	Ventricular septal defect 3		HP:0003577	PMID:21637914;PMID:20659440;PMID:21110066	PCS		5/5			C	HPO:probinson[2022-09-08]
OMIM:614432	Ventricular septal defect 3		HP:0001629	PMID:21637914;PMID:20659440;PMID:21110066	PCS		5/5			P	HPO:probinson[2022-09-08];HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:614432	Ventricular septal defect 3		HP:0001643	PMID:21110066	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:614432	Ventricular septal defect 3		HP:0001631	PMID:21637914	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:614432	Ventricular septal defect 3		HP:0000006	PMID:21110066	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:614432	Ventricular septal defect 3		HP:0004415	PMID:21637914	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:601759	Preaxial hallucal polydactyly		HP:0000819	OMIM:601759	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601759	Preaxial hallucal polydactyly		HP:0001177	OMIM:601759	IEA					P	HPO:iea[2009-02-17]
OMIM:601759	Preaxial hallucal polydactyly		HP:0001841	OMIM:601759	IEA					P	HPO:iea[2009-02-17]
OMIM:617885	Body mass index quantitative trait locus 19		HP:0002155	PMID:29311637	PCS		1/3			P	HPO:probinson[2022-09-23]
OMIM:617885	Obesity, susceptibility to, BMIQ19		HP:0003077	PMID:29311637	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-23]
OMIM:617885	Body mass index quantitative trait locus 19		HP:0002591	PMID:29311637	PCS		4/4			P	HPO:probinson[2022-09-23]
OMIM:617885	Body mass index quantitative trait locus 19		HP:0003593	PMID:29311637	PCS					C	HPO:probinson[2022-09-23];HPO:probinson[2022-09-23]
OMIM:617885	Body mass index quantitative trait locus 19		HP:0031793	PMID:29311637	PCS		3/3			P	HPO:probinson[2022-09-23]
OMIM:617885	Body mass index quantitative trait locus 19		HP:0011463	PMID:29311637	PCS					C	HPO:probinson[2022-09-23];HPO:probinson[2022-09-23]
OMIM:617885	Obesity, susceptibility to, BMIQ19		HP:0000855	PMID:29311637	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:617885	Obesity, susceptibility to, BMIQ19		HP:0000458	PMID:29311637	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:617885	Obesity, susceptibility to, BMIQ19		HP:0004409	PMID:29311637	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:617885	Obesity, susceptibility to, BMIQ19		HP:0000007	PMID:29311637	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-23]
OMIM:617885	Obesity, susceptibility to, BMIQ19		HP:0001249	PMID:29311637	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-23]
OMIM:617885	Obesity, susceptibility to, BMIQ19		HP:0001513	PMID:29311637	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-23]
OMIM:617885	Body mass index quantitative trait locus 19		HP:0000842	PMID:29311637	PCS		1/3			P	HPO:probinson[2022-09-23]
OMIM:605259	Spinocerebellar ataxia 13		HP:0000365	OMIM:605259	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:605259	Spinocerebellar ataxia 13		HP:0003596	PMID:23912307	PCS					C	HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001272	OMIM:605259	IEA		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001260	PMID:23912307	PCS		10/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0002066	PMID:23912307	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001252	OMIM:605259	IEA					P	HPO:iea[2009-02-17]
OMIM:605259	Spinocerebellar ataxia 13		HP:0002062	OMIM:605259	IEA					P	HPO:iea[2009-02-17]
OMIM:605259	Spinocerebellar ataxia 13		HP:0002073	OMIM:605259	IEA					P	HPO:iea[2009-02-17]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001270	OMIM:605259	IEA					P	HPO:iea[2009-02-17]
OMIM:605259	Spinocerebellar ataxia 13		HP:0002070	PMID:23912307	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0100543	PMID:23912307	PCS		14/21			P	HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0000639	PMID:23912307	PCS		0/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0011462	PMID:23912307	PCS					C	HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0008003	OMIM:605259	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605259	Spinocerebellar ataxia 13		HP:0007256	OMIM:605259	TAS					P	HPO:skoehler[2015-01-04]
OMIM:605259	Spinocerebellar ataxia 13		HP:0000648	OMIM:605259	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605259	Spinocerebellar ataxia 13		HP:0002406	OMIM:605259	IEA					P	HPO:iea[2009-02-17]
OMIM:605259	Spinocerebellar ataxia 13		HP:0006886	PMID:23912307	PCS		6/12			P	HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001257	PMID:23912307	PCS		1/12			P	HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0000006	PMID:23912307	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001249	OMIM:605259	IEA					P	HPO:skoehler[2010-06-20]
OMIM:605259	Spinocerebellar ataxia 13		HP:0003677	OMIM:605259	IEA					C	HPO:iea[2009-02-17]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001347	PMID:23912307	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-09]
OMIM:605259	Spinocerebellar ataxia 13		HP:0001336	PMID:23912307	PCS		2/12			P	HPO:probinson[2022-11-09]
OMIM:269160	SCHIZENCEPHALY		HP:0002120	PMID:26576802	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:269160	SCHIZENCEPHALY		HP:0001274	PMID:26576802	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:269160	SCHIZENCEPHALY		HP:0010636	OMIM:269160	IEA					P	HPO:skoehler[2015-01-19]
OMIM:301035	Hypothyroidism, congenital, nongoitrous, 9		HP:0004322	PMID:30061370	PCS					P	HPO:probinson[2020-07-24]
OMIM:301035	Hypothyroidism, congenital, nongoitrous, 9		HP:0033075	PMID:30061370	PCS					P	HPO:probinson[2020-10-13]
OMIM:301035	Hypothyroidism, congenital, nongoitrous, 9		HP:0001419	PMID:30061370	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:301035	Hypothyroidism, congenital, nongoitrous, 9		HP:0033078	PMID:30061370	PCS					P	HPO:probinson[2020-10-13]
OMIM:301035	Hypothyroidism, congenital, nongoitrous, 9		HP:0005990	PMID:30061370	PCS		9/17			P	HPO:probinson[2020-10-13]
OMIM:301035	Hypothyroidism, congenital, nongoitrous, 9		HP:0003623	PMID:30061370	PCS					C	HPO:probinson[2020-07-24]
OMIM:301035	Hypothyroidism, congenital, nongoitrous, 9		HP:0011787	PMID:30061370	PCS					P	HPO:probinson[2020-07-24]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001397	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000065	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001176	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0003577	PMID:15181077	PCS		6/8			C	HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001394	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0002240	PMID:15181077	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0003292	PMID:15181077;PMID:11967537	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000819	PMID:15181077;PMID:11967537	PCS		17/28			P	HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0003809	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0011463	PMID:15181077	PCS		1/8			C	HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000877	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0009125	OMIM:608594	TAS					P	HPO:probinson[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000956	PMID:15181077	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001544	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0002833	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0002910	OMIM:608594	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001007	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001744	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001249	PMID:15181077	PCS		0/6			P	HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0003623	PMID:15181077	PCS		1/8			C	HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000098	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0002155	PMID:15181077	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0002591	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001735	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0003716	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001537	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000007	PMID:11967537	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001833	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0001638	OMIM:608594	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000868	OMIM:608594	TAS					P	HPO:probinson[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0025128	OMIM:608594	TAS					P	HP:probinson[2019-01-22]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0003758	OMIM:608594	TAS					P	HP:probinson[2019-01-22]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0008665	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0005616	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000400	OMIM:608594	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000147	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000842	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000303	OMIM:608594	IEA					P	HPO:iea[2009-02-17]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000787	OMIM:608594	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608594	Lipodystrophy, congenital generalized, type 1		HP:0000325	OMIM:608594	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618787	Deafness, autosomal dominant 76		HP:0001751	PMID:31432506	PCS		0/4			P	HPO:probinson[2020-05-10];HPO:probinson[2024-03-16]
OMIM:618787	Deafness, autosomal dominant 76		HP:0000407	PMID:31432506	PCS		4/4			P	HPO:probinson[2020-05-10];HPO:probinson[2024-03-16]
OMIM:618787	Deafness, autosomal dominant 76		HP:0003593	PMID:31432506	PCS					C	HPO:probinson[2024-03-16]
OMIM:618787	Deafness, autosomal dominant 76		HP:0001270	PMID:31432506	PCS		0/4			P	HPO:probinson[2024-03-16]
OMIM:618787	Deafness, autosomal dominant 76		HP:0002403	PMID:31432506	PCS		0/4			P	HPO:probinson[2024-03-16]
OMIM:618787	Deafness, autosomal dominant 76		HP:0000006	PMID:31397523	PCS					I	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0032945	PMID:38096951	PCS		5/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0003774	PMID:38096951	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0003596	PMID:38096951	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0032948	PMID:38096951	PCS		4/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0003124	PMID:38096951	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0000790	PMID:38096951	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0000096	PMID:38096951	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0033499	PMID:38096951	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0033289	PMID:38096951	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0000093	PMID:38096951	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0000092	PMID:38096951	PCS		7/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0012213	PMID:38096951	PCS		8/8			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0012622	PMID:38096951	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0031264	PMID:38096951	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0000822	PMID:38096951	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0001997	PMID:38096951	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621106	Tubulointerstitial kidney disease, autosomal dominant 6		HP:0000006	PMID:38096951	PCS					I	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0003676	PMID:19439420	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0002166	PMID:19439420	PCS		15/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0003596	PMID:19439420	PCS		1/16			C	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0000020	PMID:19439420	PCS		10/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0002064	PMID:19439420	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0002061	PMID:19439420	PCS		16/16			P	HPO:probinson[2017-05-29];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0100543	OMIM:270800	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0000518	OMIM:270800	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0000639	OMIM:270800	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0007340	PMID:19439420	PCS		14/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0011463	PMID:19439420	PCS		3/16			C	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0011462	PMID:19439420	PCS		6/16			C	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0003107	PMID:19439420	PCS		0/9			P	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0009129	PMID:19439420	PCS		2/16			P	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0001347	PMID:19439420	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0003621	PMID:19439420	PCS		6/16			C	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0006858	OMIM:270800	TAS					P	HPO:probinson[2012-04-28]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0002650	PMID:19439420	PCS		2/16			P	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0001761	PMID:19439420	PCS		7/16			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0003487	PMID:19439420	PCS		15/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0003484	PMID:19439420	PCS		4/16			P	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0001260	OMIM:270800	IEA					P	HPO:iea[2009-02-17]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0002174	PMID:19439420	PCS		1/16			P	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0000407	OMIM:270800	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0007210	PMID:19439420	PCS		6/16			P	HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0030890	PMID:19439420	PCS		3/6			P	HPO:probinson[2017-05-29]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0001317	OMIM:270800	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0000007	PMID:19439420	PCS					I	HPO:iea[2009-02-17]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0000648	OMIM:270800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0002406	PMID:19439420	PCS	HP:0003596	4/16			P	HPO:probinson[2017-05-29];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0001258	PMID:19439420	PCS					P	HPO:probinson[2012-04-28];HPO:probinson[2022-04-30]
OMIM:270800	Spastic paraplegia 5A, autosomal recessive		HP:0006986	PMID:19439420	PCS		2/16			P	HPO:probinson[2022-04-30]
OMIM:114480	Breast cancer		HP:0003002	OMIM:114480	IEA					P	HPO:iea[2009-02-17]
OMIM:114480	Breast cancer		HP:0001442	OMIM:114480	IEA					I	HPO:skoehler[2019-02-22]
OMIM:114480	Breast cancer		HP:0000006	OMIM:114480	IEA					I	HPO:iea[2009-02-17]
OMIM:134750	Felty syndrome		HP:0001370	OMIM:134750	IEA					P	HPO:iea[2009-02-17]
OMIM:134750	Felty syndrome		HP:0000006	OMIM:134750	IEA					I	HPO:iea[2009-02-17]
OMIM:134750	Felty syndrome		HP:0001744	OMIM:134750	IEA					P	HPO:iea[2009-02-17]
OMIM:134750	Felty syndrome		HP:0001875	OMIM:134750	IEA					P	HPO:iea[2009-02-17]
OMIM:618793	Intellectual developmental disorder 62		HP:0001166	PMID:29460436	PCS					P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0000486	PMID:29460436	PCS		2/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0002650	PMID:29460436	PCS		3/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0001250	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0001382	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0001065	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0003593	PMID:29460436	PCS					C	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0012771	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0001519	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0000729	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0001763	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0000006	PMID:29460436	PCS					I	HPO:probinson[2020-05-08];HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0001249	PMID:29460436	PCS		3/3			P	HPO:probinson[2020-05-08]
OMIM:618793	Intellectual developmental disorder 62		HP:0006855	PMID:29460436	PCS		1/3			P	HPO:probinson[2020-05-08]
OMIM:159580	Myelopathy, htlv-1-associated		HP:0002196	OMIM:159580	TAS					P	HPO:probinson[2009-02-17]
OMIM:159580	Myelopathy, htlv-1-associated		HP:0007256	OMIM:159580	TAS					P	HPO:probinson[2014-11-15]
OMIM:159580	Myelopathy, htlv-1-associated		HP:0002313	OMIM:159580	TAS					P	HPO:probinson[2014-11-15]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0003577	PMID:26741492	PCS		1/1			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0001582	PMID:26741492	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0001635	PMID:26741492	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0011923	PMID:26741492	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0001417	PMID:26741492	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0001511	PMID:26741492	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0003811	PMID:26741492	PCS		1/1			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0001942	PMID:26741492	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:301021	Mitochondrial complex I deficiency, nuclear type 30		HP:0001622	PMID:26741492	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:231690	Glutaric aciduria III		HP:0002014	OMIM:231690	TAS					P	HPO:skoehler[2015-06-22]
OMIM:231690	Glutaric aciduria III		HP:0002013	OMIM:231690	TAS					P	HPO:skoehler[2015-06-22]
OMIM:231690	Glutaric aciduria III		HP:0001508	OMIM:231690	IEA					P	HPO:iea[2009-02-17]
OMIM:231690	Glutaric aciduria III		HP:0000836	OMIM:231690	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:231690	Glutaric aciduria III		HP:0003150	PMID:18926513	PCS		6/6			P	HPO:iea[2009-02-17]
OMIM:231690	Glutaric aciduria III		HP:0000822	OMIM:231690	TAS					P	HPO:skoehler[2015-06-22]
OMIM:231690	Glutaric aciduria III		HP:0000007	PMID:18926513	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:231690	Glutaric aciduria III		HP:0034688	PMID:1909402	PCS					P	HPO:probinson[2023-03-31]
OMIM:231690	Glutaric aciduria III		HP:0000853	OMIM:231690	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0003774	OMIM:614817	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0003676	PMID:22772369	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0001970	PMID:22772369	PCS		9/9			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0032948	PMID:22772369	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0000790	PMID:22772369	PCS		1/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0003076	PMID:22772369	PCS		5/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0000090	PMID:22772369	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0000093	PMID:22772369	PCS		5/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0041050	PMID:22772369	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0000007	PMID:22772369	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0002910	PMID:22772369	PCS		5/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0003259	PMID:22772369	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614817	Interstitial nephritis, karyomegalic		HP:0003138	PMID:22772369	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-28]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003236	PMID:31837156	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003596	PMID:31837156	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0030674	PMID:24126608	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0001252	PMID:31090908;PMID:31837156;PMID:24126608	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0002460	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003390	PMID:31090908;PMID:30847374;PMID:24126608	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0001270	PMID:24126608	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0100297	PMID:24126608	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0012110	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		0/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0000639	PMID:24126608	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0011463	PMID:24126608	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0007002	PMID:31090908;PMID:30847374;PMID:24126608	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0025336	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003701	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0001347	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0001765	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003202	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0001265	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0032989	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0000252	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003621	PMID:31090908;PMID:30847374	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0002650	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0001761	PMID:30847374;PMID:31837156	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003487	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0001321	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		0/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003380	PMID:24126608	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0000007	PMID:24126608	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0009879	PMID:31090908;PMID:30847374;PMID:31837156;PMID:24126608	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620542	Neuronopathy, distal hereditary motor, autosomal recessive 10		HP:0003557	PMID:24126608	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003236	PMID:16247064	PCS		1/3			P	HPO:probinson[2012-04-11];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0010628	OMIM:167320	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0008946	PMID:16247064	PCS		4/4			P	HPO:probinson[2012-04-11];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003596	PMID:15732117;PMID:16247064	PCS		4/5			C	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0001332	OMIM:167320	IEA					P	HPO:iea[2009-02-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0002145	OMIM:167320	IEA					P	HPO:iea[2009-02-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003693	OMIM:167320	IEA					P	HPO:iea[2009-02-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003198	PMID:16247064	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003551	OMIM:167320	IEA					P	HPO:iea[2009-02-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003691	OMIM:167320	IEA					P	HPO:iea[2009-02-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0034159	PMID:15732117;PMID:16247064	PCS		4/5			P	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0002381	OMIM:167320;PMID:15732117	PCS		11/11			P	HPO:probinson[2022-05-30];HPO:skoehler[2012-11-21]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003690	OMIM:167320	TAS					P	HPO:probinson[2012-04-11]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0030838	OMIM:167320	TAS					P	HPO:skoehler[2017-07-13]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0012444	PMID:15732117	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0002938	OMIM:167320	IEA					P	HPO:iea[2009-02-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003749	PMID:16247064	PCS		4/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003805	PMID:16247064	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0025710	PMID:16247064	PCS		1/4			C	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003701	PMID:16247064	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003547	PMID:16247064	PCS		3/4			P	HPO:probinson[2012-04-11];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003724	PMID:16247064	PCS		3/4			P	HPO:probinson[2012-04-11];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003700	PMID:15732117	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0010639	OMIM:167320	TAS					P	HPO:probinson[2012-04-11]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0006913	OMIM:167320	IEA					P	HPO:iea[2012-01-01]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0001288	OMIM:167320	TAS					P	HPO:skoehler[2012-10-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0002273	PMID:15732117	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0009073	PMID:15732117	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0000726	PMID:15732117;PMID:16247064	PCS		1/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-30];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0007112	OMIM:167320	IEA					P	HPO:iea[2012-01-01]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0003418	PMID:16247064	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0002505	PMID:16247064	PCS	HP:0003596	2/4			P	HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0000006	PMID:15034582	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0002644	OMIM:167320	IEA					P	HPO:iea[2009-02-17]
OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1		HP:0008988	PMID:16247064	PCS		4/4			P	HPO:probinson[2012-04-11];HPO:probinson[2022-05-30]
OMIM:178200	Pterygium, antecubital		HP:0001377	OMIM:178200	IEA					P	HPO:iea[2009-02-17]
OMIM:178200	Pterygium, antecubital		HP:0009760	OMIM:178200	TAS					P	HPO:probinson[2013-04-12]
OMIM:178200	Pterygium, antecubital		HP:0005829	OMIM:178200	IEA					P	HPO:iea[2009-02-17]
OMIM:178200	Pterygium, antecubital		HP:0005739	OMIM:178200	IEA					P	HPO:iea[2009-02-17]
OMIM:178200	Pterygium, antecubital		HP:0000006	OMIM:178200	IEA					I	HPO:iea[2009-02-17]
OMIM:135300	Fibromatosis, gingival, 1		HP:0000365	PMID:11868160	PCS		0/38			P	HPO:probinson[2022-03-19]
OMIM:135300	Fibromatosis, gingival, 1		HP:0000169	PMID:11868160	PCS		38/38			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-19]
OMIM:135300	Fibromatosis, gingival, 1		HP:0000006	PMID:11868160	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-19]
OMIM:135300	Fibromatosis, gingival, 1		HP:0001249	PMID:11868160	PCS		0/38			P	HPO:probinson[2022-03-19]
OMIM:602085	Polydactyly, postaxial, type A2		HP:0001162	OMIM:602085	IEA					P	HPO:iea[2009-02-17]
OMIM:602085	Polydactyly, postaxial, type A2		HP:0000006	OMIM:602085	IEA					I	HPO:iea[2009-02-17]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0002345	PMID:22912398	PCS		2/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0003577	PMID:22912398	PCS		1/2			C	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0003698	OMIM:302500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0002015	PMID:22912398	PCS		1/2			P	HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0003621	OMIM:302500	IEA					C	HPO:iea[2009-02-17]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0000486	OMIM:302500	TAS					P	HPO:skoehler[2013-01-21]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0001272	PMID:22912398	PCS		2/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0001260	PMID:22912398	PCS		1/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0001252	PMID:22912398	PCS		1/2			P	HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0003680	OMIM:302500	TAS					C	HPO:skoehler[2013-01-21]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0001251	PMID:22912398	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0003593	PMID:22912398	PCS		1/2			C	HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0001270	PMID:22912398	PCS		2/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0002071	PMID:22912398	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0002080	PMID:22912398	PCS		2/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0000639	OMIM:302500	IEA					P	HPO:iea[2009-02-17]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0001419	PMID:22912398	PCS					I	HPO:skoehler[2013-01-21];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0000514	PMID:22912398	PCS		1/2			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-26]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0001319	OMIM:302500	TAS					P	HPO:skoehler[2013-01-21]
OMIM:302500	Spinocerebellar ataxia, X-linked 1		HP:0002317	PMID:22912398	PCS		2/2			P	HPO:probinson[2023-02-26];HPO:probinson[2023-02-26]
OMIM:614181	Retinitis pigmentosa 62		HP:0007737	PMID:21835304	PCS		3/4			P	HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0000662	PMID:21835304	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0003596	PMID:21835304	PCS		2/8			C	HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0001123	PMID:21835304	PCS		7/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0011462	PMID:21835304	PCS		6/8			C	HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0000007	PMID:21835304	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0007663	PMID:21835304	PCS		8/8			P	HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0000543	PMID:21835304	PCS		2/8			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0000510	PMID:21835304	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0007843	PMID:21835304	PCS		4/8			P	HPO:probinson[2022-11-06]
OMIM:614181	Retinitis pigmentosa 62		HP:0011504	PMID:21835304	PCS		1/8			P	HPO:probinson[2022-11-06]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0002069	PMID:31278393	PCS		2/7			P	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000486	PMID:31278393	PCS		3/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001250	PMID:31278393	PCS		8/8			P	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001252	PMID:31278393	PCS		7/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0030891	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0012469	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0010055	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001763	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001249	PMID:31278393	PCS		7/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000996	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001385	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000054	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001344	PMID:31278393	PCS		5/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001266	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000490	PMID:31278393	PCS		3/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001263	PMID:31278393	PCS		8/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000294	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0011800	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001182	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000729	PMID:31278393	PCS		4/6			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000767	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0004209	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0008445	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0009778	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000322	PMID:31278393	PCS		3/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0002305	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000006	PMID:31278393	PCS					I	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000324	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001776	PMID:31278393	PCS		2/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0004467	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000582	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000463	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0002121	PMID:31278393	PCS		4/7			P	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000262	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0031491	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0007021	PMID:31278393	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000337	PMID:31278393	PCS		4/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000414	PMID:31278393	PCS		2/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001943	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0002119	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000218	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000577	PMID:31278393	PCS		2/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000154	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000473	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000750	PMID:31278393	PCS		8/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0003189	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0002650	PMID:31278393	PCS		3/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0031936	PMID:31278393	PCS		8/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0006915	PMID:31278393	PCS		2/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000470	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0005280	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0011304	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000506	PMID:31278393	PCS		1/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0007099	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000508	PMID:31278393	PCS		2/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0001357	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000347	PMID:31278393	PCS		4/7			P	HPO:probinson[2023-06-15]
OMIM:620224	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures		HP:0000028	PMID:31278393	PCS		1/8			P	HPO:probinson[2023-06-15]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0000252	OMIM:300471	IEA					P	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0000494	OMIM:300471	IEA					P	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0001250	OMIM:300471	IEA					P	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0000490	OMIM:300471	IEA					P	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0001419	OMIM:300471	IEA					I	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0001999	OMIM:300471	IEA					P	HPO:skoehler[2015-01-19]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0001956	OMIM:300471	IEA					P	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0002967	OMIM:300471	IEA					P	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0000322	OMIM:300471	IEA					P	HPO:iea[2009-02-17]
OMIM:300471	Cubitus valgus with impaired intellectual development and unusual facies		HP:0000995	OMIM:300471	TAS					P	HPO:probinson[2009-02-17]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0002014	PMID:32163377	PCS					P	HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001894	PMID:32163377	PCS					P	HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0020086	PMID:32163377	PCS	HP:0003593	1/2			P	HPO:probinson[2024-03-16]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0020087	PMID:32163377	PCS	HP:0003593	1/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14];HPO:probinson[2024-03-16]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0003593	PMID:32163377	PCS		2/2			C	HPO:probinson[2024-03-16]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0003281	PMID:32163377	PCS					P	HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0012156	PMID:32163377	PCS		0/1			P	HPO:probinson[2020-08-14];HPO:probinson[2024-03-16]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001508	PMID:32163377	PCS	HP:0003593				P	HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001903	PMID:32163377	PCS		2/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0000007	PMID:32163377	PCS					I	HPO:probinson[2020-08-14];HPO:probinson[2022-12-03]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001945	PMID:32163377	PCS		2/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0000988	PMID:32163377	PCS					P	HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001433	PMID:32163377	PCS		2/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001876	PMID:32163377	PCS					P	HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001744	PMID:32163377	PCS					P	HPO:probinson[2020-08-14]
OMIM:618963	Immunodeficiency 69, mycobacteriosis		HP:0001974	PMID:32163377	PCS		2/2			P	HPO:probinson[2020-08-14];HPO:probinson[2020-08-14]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0003621	PMID:17689125	PCS		1/13			C	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0002155	OMIM:306000	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0003124	OMIM:306000	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:306000	Glycogen storage disease, type IXa1		HP:6000333	PMID:21634085	PCS					P	HPO:probinson[2024-02-27]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0001252	PMID:17689125	PCS		2/15		HP:0012825	P	HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0002240	PMID:17689125	PCS		10/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0003593	PMID:17689125	PCS		4/13			C	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0001270	PMID:17689125	PCS		1/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0012378	PMID:17689125	PCS		3/15			P	HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0001419	PMID:17689125	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0011463	PMID:17689125	PCS		8/13			C	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0001943	PMID:17689125	PCS		10/15			P	HPO:probinson[2012-05-05];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0001946	OMIM:306000	IEA		5/11		HP:0025212	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0001510	OMIM:306000	IEA					P	HPO:iea[2009-02-17]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0002910	OMIM:306000	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0001744	PMID:17689125	PCS		2/15			P	HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0003128	PMID:17689125	PCS		5/12			P	HPO:probinson[2022-04-30]
OMIM:306000	Glycogen storage disease, type IXa1		HP:0002149	PMID:17689125	PCS		1/5			P	HPO:probinson[2022-04-30]
OMIM:618977	Optic atrophy 12		HP:0002487	PMID:32219868	PCS		1/23			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0003477	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000365	PMID:29181157;PMID:32219868	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001256	PMID:29181157;PMID:26539208;PMID:32219868	PCS		2/25			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0003596	PMID:32219868	PCS		4/11			C	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001332	PMID:32219868	PCS		2/22			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0002066	PMID:32219868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:6000397	PMID:32600459	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001252	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001251	PMID:29181157;PMID:26539208;PMID:32600459;PMID:32219868	PCS		1/24			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0002064	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000716	PMID:32219868	PCS		1/23			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000639	PMID:32219868	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0011463	PMID:32600459;PMID:32219868	PCS		5/12			C	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0011462	PMID:32219868	PCS		1/11			C	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000618	PMID:32219868	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000613	PMID:29181157;PMID:26539208	PCS		2/2			P	HPO:probinson[2020-09-04];ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0007641	PMID:29181157	PCS		1/1			P	HPO:probinson[2020-09-04]
OMIM:618977	Optic atrophy 12		HP:0007663	PMID:29181157;PMID:26539208;PMID:32600459;PMID:32219868	PCS		18/22			P	HPO:probinson[2020-09-04];ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000597	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000575	PMID:26539208	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000512	PMID:29181157;PMID:32600459	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0007305	PMID:32600459	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0002313	PMID:32219868	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001347	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000473	PMID:32219868	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0002059	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0006934	PMID:26539208;PMID:32219868	PCS		1/24			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0003621	PMID:29181157;PMID:26539208;PMID:32219868	PCS		4/13			C	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0008619	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000551	PMID:32219868	PCS		20/22			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0030586	PMID:29181157	PCS					P	HPO:probinson[2020-09-04]
OMIM:618977	Optic atrophy 12		HP:0002072	PMID:32219868	PCS		1/23			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0020119	PMID:32219868	PCS		22/22			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000649	PMID:29181157;PMID:32600459	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000407	PMID:26539208;PMID:32219868	PCS		4/22			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001317	PMID:32219868	PCS		0/23			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0009830	PMID:29181157	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000648	PMID:29181157;PMID:32600459;PMID:32219868	PCS		7/7			P	HPO:probinson[2020-09-04];ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000543	PMID:29181157;PMID:26539208;PMID:32600459;PMID:32219868	PCS		8/8			P	HPO:probinson[2020-09-04];ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000642	PMID:26539208	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001257	PMID:29181157;PMID:26539208;PMID:32219868	PCS		1/24			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0000006	PMID:32600459	PCS					I	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:618977	Optic atrophy 12		HP:0000501	PMID:32219868	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:618977	Optic atrophy 12		HP:0001336	PMID:32219868	PCS		1/23			P	ORCID:0000-0002-0736-9199[2025-10-19]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0011818	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0003577	PMID:15051220	PCS		1/1			C	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0000585	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0002321	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0007906	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0012506	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0007291	PMID:15051220	PCS		1/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0011483	PMID:15051220	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0000316	PMID:15051220	PCS		2/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0007663	PMID:15051220	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0000238	PMID:15051220	PCS		1/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0002119	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0007676	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0000543	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0002315	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0007700	PMID:15051220	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0000377	PMID:15051220	PCS		3/3			P	HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0000006	PMID:15051220	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0000512	PMID:15051220	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-04]
OMIM:614195	Craniofacial anomalies and anterior segment dysgenesis syndrome		HP:0008625	PMID:15051220	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001254	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0004864	OMIM:557000	IEA					P	HPO:iea[2009-02-17]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001399	PMID:2243133	PCS		3/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002024	OMIM:557000	IEA					P	HPO:iea[2009-02-17]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0000980	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0011859	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002240	PMID:2243133	PCS		4/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0003593	PMID:2243133	IEA		3/5			C	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0010783	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0100651	PMID:7680315	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001908	PMID:7680315	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001508	PMID:7680315;PMID:2243133	PCS		3/6			P	HPO:probinson[2022-03-27];HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002719	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001903	PMID:501502;PMID:2243133	PCS		6/9			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0011461	PMID:2243133	PCS		1/5			C	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001944	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001427	PMID:2243133	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001789	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0008336	PMID:7680315	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001924	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0006577	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002910	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001942	PMID:2243133	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002039	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0003128	PMID:7680315;PMID:2243133	PCS		3/6			P	HPO:probinson[2022-03-27];HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0003623	PMID:2243133	PCS		1/5			C	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0003344	PMID:1447663	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002013	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002570	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002150	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0100732	PMID:501502	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0003819	PMID:7680315	PCS		1/1			C	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001738	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001518	PMID:7680315	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002904	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0011473	PMID:2243133	PCS		1/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001896	PMID:501502;PMID:2243133	PCS		5/9			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001994	PMID:7680315	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001873	PMID:2243133	PCS		3/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001876	PMID:2243133	PCS		2/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0002028	PMID:2243133	PCS		3/5			P	HPO:probinson[2022-03-27]
OMIM:557000	Pearson marrow-pancreas syndrome		HP:0001875	PMID:2243133	PCS		3/5			P	HPO:probinson[2022-03-27]
OMIM:611953	Macular degeneration, age-related, 11		HP:0000608	OMIM:611953	TAS	HP:0003584				P	HP:probinson[2018-07-08]
OMIM:611953	Macular degeneration, age-related, 11		HP:0010982	OMIM:611953	IEA					I	HPO:probinson[2013-04-03]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0008839	PMID:29769720	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0000882	PMID:29769720	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0002057	PMID:29769720	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0030674	PMID:29769720	PCS		4/4			C	HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0000007	PMID:29769720	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0009777	PMID:29769720	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0000278	PMID:29769720	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0000894	OMIM:618022	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0002987	PMID:29769720	PCS		1/4			P	HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0000776	PMID:29769720	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0001776	PMID:29769720	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-18]
OMIM:618022	Humerofemoral hypoplasia with radiotibial ray deficiency		HP:0003865	PMID:29769720	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-18]
OMIM:615506	Telangiectasia, hereditary hemorrhagic, type 5		HP:0001409	PMID:23972370	PCS		1/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-05-07]
OMIM:615506	Telangiectasia, hereditary hemorrhagic, type 5		HP:0001009	PMID:23972370	PCS		3/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-05-07]
OMIM:615506	Telangiectasia, hereditary hemorrhagic, type 5		HP:0004406	PMID:23972370	PCS		3/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-05-07]
OMIM:615506	Telangiectasia, hereditary hemorrhagic, type 5		HP:0002910	PMID:23972370	PCS		1/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-05-07]
OMIM:615506	Telangiectasia, hereditary hemorrhagic, type 5		HP:0000006	PMID:23972370	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2020-05-07]
OMIM:612269	Epilepsy, childhood absence, susceptibility to, 5		HP:0002121	PMID:18514161	PCS	HP:0011463				P	HPO:skoehler[2013-01-10];HPO:probinson[2020-07-24]
OMIM:612269	Epilepsy, childhood absence, susceptibility to, 5		HP:0003829	PMID:18514161	PCS					I	HPO:probinson[2020-07-24]
OMIM:612269	Epilepsy, childhood absence, susceptibility to, 5		HP:0000006	PMID:18514161	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-24]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002021	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002780	PMID:19836010	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001252	PMID:19836010	PCS		3/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002020	PMID:19836010	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000954	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000239	PMID:19836010	PCS		2/3			P	HPO:probinson[2022-12-21];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000316	PMID:19836010	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002617	OMIM:613177	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002779	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000835	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001522	PMID:19836010	PCS		2/4			C	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000278	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0005328	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001601	PMID:19836010	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002035	PMID:19836010	PCS		1/4			P	HPO:skoehler[2013-05-29];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001541	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001382	PMID:19836010	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0011968	PMID:19836010	PCS		3/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001582	PMID:19836010	PCS		3/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0012619	PMID:19836010	PCS		3/3			P	HPO:probinson[2022-12-21];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0011800	PMID:19836010	PCS		1/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0100539	PMID:19836010	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001537	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000007	PMID:19836010	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0004969	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001615	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001852	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001655	PMID:19836010	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000126	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000340	PMID:19836010	PCS		1/4			P	HPO:skoehler[2013-03-08];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0003577	PMID:19836010	PCS		4/4			C	HPO:probinson[2022-12-21];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002089	PMID:19836010	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000343	PMID:19836010	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000023	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0100750	PMID:19836010	PCS		2/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000938	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000778	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0006532	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001747	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001667	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001623	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000973	PMID:19836010	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000431	PMID:19836010	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000272	PMID:19836010	PCS		1/4			P	HPO:skoehler[2013-03-08];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0002097	PMID:19836010	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0025194	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0025193	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0003819	PMID:19836010	PCS		1/4			C	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000268	PMID:19836010	PCS		1/4			P	HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0001510	PMID:19836010	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-21]
OMIM:613177	Cutis laxa, autosomal recessive, type IC		HP:0000347	PMID:19836010	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-21]
OMIM:614618	Hyperekplexia 3		HP:0002069	PMID:16751771	PCS		2/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0002267	PMID:16751771	PCS		6/6			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0002036	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0001276	PMID:16751771	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0003552	PMID:16751771	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0001263	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0002020	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0011412	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0012420	PMID:16751771	PCS		2/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0000007	PMID:16751771	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0001279	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0002104	PMID:16751771	PCS	HP:0003623	1/6			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0000006	PMID:16751771	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0001348	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0001336	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0003623	PMID:16751771	PCS		6/6			C	HPO:probinson[2022-10-07];HPO:probinson[2022-10-07]
OMIM:614618	Hyperekplexia 3		HP:0005943	PMID:16751771	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0002069	PMID:21979934	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0003577	PMID:21979934	PCS		1/3			C	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0001561	PMID:21979934	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0001520	PMID:21979934	PCS		1/3			P	HPO:skoehler[2013-01-22]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0000771	PMID:21979934	PCS		1/2	MALE		P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0003593	PMID:21979934	PCS		2/3			C	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0003162	PMID:21979934	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0001943	PMID:21979934	PCS		2/3			P	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0001998	PMID:21979934	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0001528	PMID:21979934	PCS		1/3			P	HPO:skoehler[2013-01-22]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0001956	OMIM:240900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0040216	PMID:21979934	PCS		3/3			P	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0000006	PMID:21979934	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0001513	PMID:21979934	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:240900	Hypoinsulinemic hypoglycemia with hemihypertrophy		HP:0000324	PMID:21979934	PCS		1/3			P	HPO:probinson[2023-04-08]
OMIM:613611	Choanal atresia and lymphedema		HP:0000453	PMID:20826270	PCS	HP:0003577	7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613611	Choanal atresia and lymphedema		HP:0000007	PMID:20826270	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613611	Choanal atresia and lymphedema		HP:0000218	OMIM:613611	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613611	Choanal atresia and lymphedema		HP:0001698	OMIM:613611	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613611	Choanal atresia and lymphedema		HP:0001004	PMID:20826270	PCS	HP:0011463	5/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-06]
OMIM:237550	Hyperbilirubinemia, conjugated, type III		HP:0002908	OMIM:237550	IEA					P	HPO:iea[2009-02-17]
OMIM:237550	Hyperbilirubinemia, conjugated, type III		HP:0000007	OMIM:237550	IEA					I	HPO:iea[2009-02-17]
OMIM:237550	Hyperbilirubinemia, conjugated, type III		HP:0000952	OMIM:237550	IEA					P	HPO:iea[2009-02-17]
OMIM:125852	Diabetes mellitus, insulin-dependent, 2		HP:0025708	PMID:18192540	PCS		2/2			C	HPO:probinson[2023-03-01]
OMIM:125852	Diabetes mellitus, insulin-dependent, 2		HP:0100651	PMID:18192540	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-01]
OMIM:125852	Diabetes mellitus, insulin-dependent, 2		HP:0000006	PMID:18192540	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:609649	Trichilemmal cyst 1		HP:0000006	OMIM:609649	IEA					I	HPO:iea[2009-02-17]
OMIM:609649	Trichilemmal cyst 1		HP:0000951	OMIM:609649	IEA					P	HPO:iea[2009-02-17]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000341	PMID:31820119	PCS		3/13			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000286	PMID:31820119	PCS		1/15			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000340	PMID:31820119	PCS		2/13			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000343	PMID:31820119	PCS		1/15			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0001250	PMID:31820119	PCS		18/18			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002120	PMID:31820119	PCS		9/13			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000639	PMID:31820119	PCS		3/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000817	PMID:31820119	PCS		16/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0012450	PMID:31820119	PCS		7/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0008872	PMID:31820119	PCS		15/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002857	PMID:31820119	PCS		4/12			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0001347	PMID:31820119	PCS		11/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0008936	PMID:31820119	PCS		17/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002553	PMID:31820119	PCS		4/14			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000252	PMID:31820119	PCS		12/18			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0001344	PMID:31820119	PCS	HP:0003593	18/18			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002376	PMID:31820119	PCS		3/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002079	PMID:31820119	PCS		5/14			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002033	PMID:31820119	IEA					P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002273	PMID:31820119	PCS		4/17			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0011344	PMID:31820119	PCS	HP:0003593	18/18			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0005280	PMID:31820119	PCS		6/16			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0032988	PMID:31820119	PCS	HP:0003593	18/18			P	HPO:probinson[2020-06-09]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0009890	PMID:31820119	PCS		5/14			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0007750	PMID:31820119	PCS		2/18			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000007	PMID:31820119	TAS					I	HPO:probinson[2020-04-13];HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002205	PMID:31820119	PCS		3/14			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0002007	PMID:31820119	PCS		1/14			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000664	PMID:31820119	PCS		1/15			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0001257	PMID:31820119	PCS		7/18			P	HPO:probinson[2020-04-13]
OMIM:618744	Epileptic encephalopathy, early infantile, 83		HP:0000369	PMID:31820119	PCS		4/13			P	HPO:probinson[2020-04-13]
OMIM:604379	Hypotrichosis 7		HP:0002224	OMIM:604379	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:604379	Hypotrichosis 7		HP:0000164	PMID:17333281	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0003577	PMID:17333281	PCS		3/3			C	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0001597	PMID:17333281	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0002299	PMID:17095700	PCS					P	HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0002231	PMID:17333281	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0045075	PMID:17333281	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0008070	PMID:17333281	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0002209	PMID:17333281	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0000007	PMID:17095700	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0025249	PMID:17333281	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0000653	PMID:17333281	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0000971	PMID:17333281	PCS		0/3			P	HPO:skoehler[2013-06-10];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0000951	PMID:17333281	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-05-08]
OMIM:604379	Hypotrichosis 7		HP:0002215	PMID:17333281	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:180550	Ring dermoid of cornea		HP:0500070	PMID:7387508	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:180550	Ring dermoid of cornea		HP:0000481	OMIM:180550	TAS					P	HPO:skoehler[2012-10-16]
OMIM:180550	Ring dermoid of cornea		HP:0000646	PMID:7387508	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:180550	Ring dermoid of cornea		HP:0000502	OMIM:180550	TAS					P	HPO:skoehler[2012-10-16]
OMIM:180550	Ring dermoid of cornea		HP:0025348	PMID:7387508	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:180550	Ring dermoid of cornea		HP:0025612	PMID:7387508	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:180550	Ring dermoid of cornea		HP:0000006	OMIM:180550	TAS					I	HPO:skoehler[2012-10-16]
OMIM:248390	Treacher Collins syndrome 3		HP:0000494	PMID:21131976	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:248390	Treacher Collins syndrome 3		HP:0000175	PMID:21131976	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:248390	Treacher Collins syndrome 3		HP:0003577	PMID:21131976	PCS		3/3			C	HPO:probinson[2023-02-21]
OMIM:248390	Treacher Collins syndrome 3		HP:0005321	OMIM:248390	IEA					P	HPO:iea[2009-02-17]
OMIM:248390	Treacher Collins syndrome 3		HP:0000272	PMID:21131976	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:248390	Treacher Collins syndrome 3		HP:0008551	PMID:21131976	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-10]
OMIM:248390	Treacher Collins syndrome 3		HP:0000007	PMID:21131976	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:248390	Treacher Collins syndrome 3		HP:0000405	PMID:21131976	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-10]
OMIM:248390	Treacher Collins syndrome 3		HP:0010669	PMID:21131976	PCS		3/3			P	HPO:probinson[2022-11-10];HPO:probinson[2022-11-10]
OMIM:248390	Treacher Collins syndrome 3		HP:0000652	PMID:21131976	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:248390	Treacher Collins syndrome 3		HP:0000347	PMID:21131976	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:615274	Cataract 15, multiple types		HP:0100018	OMIM:615274	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615274	Cataract 15, multiple types		HP:0003577	PMID:10802646	PCS		18/18			C	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:615274	Cataract 15, multiple types		HP:0100019	OMIM:615274	IEA		1/18			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:615274	Cataract 15, multiple types		HP:0007971	PMID:10802646	PCS		17/18			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:615274	Cataract 15, multiple types		HP:0000006	PMID:10802646	PCS					I	HPO:probinson[2015-05-10];HPO:probinson[2023-02-19]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001332	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0003198	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001252	PMID:20374271	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001290	OMIM:615512	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001508	PMID:20374271	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0002317	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0002878	PMID:20374271	PCS		2/2			P	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001324	OMIM:615512	TAS				HP:0003676	P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001522	PMID:20374271	PCS		1/2			C	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001744	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0006579	PMID:20374271	PCS		2/2			P	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0000952	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0003623	PMID:20374271	PCS		2/2			C	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0003202	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0003323	OMIM:615512	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001562	PMID:20374271	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001265	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0002059	PMID:20374271	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0002098	PMID:20374271	PCS		2/2			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0004870	PMID:20374271	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001263	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001081	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0002093	PMID:20374271	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001082	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0011421	PMID:20374271	PCS		1/2			C	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0002808	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0009830	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001878	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001635	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0000007	PMID:20374271	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0002747	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0000543	OMIM:615512	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001257	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001895	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001972	PMID:20374271	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001337	OMIM:615512	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615512	Triosephosphate isomerase deficiency		HP:0001897	OMIM:615512	TAS					P	HPO:skoehler[2013-11-28]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001298	PMID:23714749	PCS		3/17			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000121	PMID:27536553	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003477	PMID:24190800;PMID:22508010;PMID:34979697;PMID:22964873	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000365	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002661	OMIM:256810	IEA					P	HPO:iea[2009-02-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001332	PMID:18695062;OMIM:256810	PCS		11/13			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2012-10-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0030059	PMID:20074988	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0004322	OMIM:256810	IEA					P	HPO:iea[2009-02-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003231	PMID:18695062;PMID:31664948;PMID:22824774	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002141	PMID:26437932	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002020	PMID:20074988	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003593	PMID:18695062;PMID:33486010;PMID:23829229;PMID:29318572;PMID:20074988;PMID:28209105;PMID:27536553;PMID:16909392;PMID:25129007;PMID:23714749;PMID:18329934;PMID:24894789	PCS		34/48			C	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002380	PMID:23829229;PMID:22824774	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001290	PMID:18329934	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003073	PMID:29318572;PMID:28209105;PMID:22824774;PMID:28673863	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0005010	OMIM:256810	TAS					P	HPO:iea[2009-02-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0033051	PMID:24190800;PMID:26437932;PMID:28673863	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000639	PMID:18695062;PMID:23829229;OMIM:256810	PCS		12/14			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2012-10-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002936	PMID:16909392	PCS		3/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006994	PMID:16909392	PCS		2/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002659	OMIM:256810	TAS					P	HPO:iea[2009-02-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001324	PMID:23829229;PMID:20074988;PMID:31664948	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000114	PMID:20074988	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002019	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000597	PMID:26437932;PMID:22964873	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003623	PMID:18695062;PMID:23829229;PMID:20074988;PMID:31664948;PMID:22824774	PCS		8/17			C	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002311	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000495	PMID:16909392	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0031956	PMID:23829229;PMID:27536553;PMID:28209105;PMID:22824774;PMID:26437932;PMID:24894789;PMID:34035203;PMID:18695062;PMID:29318572;PMID:31664948;PMID:16909392;PMID:34979697;PMID:18329934	PCS		21/24			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000252	PMID:18695062;PMID:20074988;PMID:23714749;PMID:24894789	PCS		4/26			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006858	PMID:24190800;PMID:22508010;PMID:34979697;PMID:28673863;PMID:26437932	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0011924	PMID:16909392	PCS		1/1			P	HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002033	PMID:31664948	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002151	PMID:18695062;PMID:29318572;PMID:20074988;PMID:27536553;PMID:22824774;PMID:25129007;PMID:26437932;PMID:34979697;PMID:23714749;PMID:28673863;PMID:22964873;PMID:24894789	PCS		29/40			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0011923	PMID:16909392;PMID:23714749	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0034397	PMID:22508010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006581	PMID:18695062;PMID:20074988;PMID:22824774;PMID:16909392;PMID:23714749	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006582	OMIM:256810	IEA					P	HPO:iea[2009-02-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000007	PMID:16582910	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001733	PMID:20074988	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001612	PMID:31664948	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001397	PMID:18695062;PMID:27536553;PMID:22508010;PMID:16909392;PMID:23714749;PMID:25129007	PCS		16/23			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001396	PMID:18695062;PMID:33486010;PMID:23829229;PMID:20074988;PMID:27536553;PMID:16909392;PMID:23714749	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003577	PMID:23714749	PCS		6/17			C	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001399	PMID:18695062;PMID:23829229;PMID:20074988;PMID:31664948;PMID:27536553;PMID:16909392;PMID:22824774;PMID:23714749;PMID:34979697;PMID:25129007	PCS		34/44			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001271	PMID:33486010;PMID:23829229;PMID:18329934	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001394	PMID:33486010;PMID:20074988;PMID:24190800;PMID:31664948;PMID:28209105;PMID:22508010;PMID:16909392;PMID:23714749;PMID:18329934	PCS		11/32			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002240	PMID:33486010;PMID:23829229;PMID:20074988;PMID:24190800;PMID:27536553;PMID:22508010;PMID:22824774;PMID:26437932;PMID:24894789;PMID:34035203;PMID:18695062;PMID:29318572;PMID:16909392;PMID:28673863;PMID:34979697;PMID:25129007	PCS		24/35			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000580	PMID:18329934;PMID:24894789	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0032653	PMID:27536553;PMID:34979697;PMID:34035203	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001270	PMID:16909392;PMID:26437932	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0012202	PMID:18695062;PMID:23829229	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0010547	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0031964	PMID:23829229;PMID:27536553;PMID:28209105;PMID:22824774;PMID:26437932;PMID:24894789;PMID:34035203;PMID:18695062;PMID:29318572;PMID:31664948;PMID:16909392;PMID:34979697;PMID:18329934	PCS		21/24			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0012573	PMID:18329934	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0007141	OMIM:256810	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0007021	OMIM:256810	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001944	PMID:18695062;PMID:23829229;PMID:22824774	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0040319	PMID:31664948	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001943	PMID:18695062;PMID:33486010;PMID:23829229;PMID:29318572;PMID:20074988;PMID:27536553;PMID:28209105;PMID:16909392;PMID:22824774;PMID:26437932;PMID:23714749;PMID:18329934	PCS		25/45			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006970	PMID:18695062;PMID:20074988;PMID:18329934	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001942	PMID:16909392	PCS		5/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006579	PMID:16909392	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003689	PMID:22508010;PMID:22964873	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003326	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002014	OMIM:256810;PMID:20074988;PMID:24894789	PCS		14/18			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2012-10-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002136	PMID:16909392	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002015	PMID:28673863	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003621	PMID:22508010;PMID:23714749;PMID:28673863;PMID:26437932	PCS		5/21			C	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002650	PMID:33486010;PMID:26437932	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002376	PMID:18329934	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001288	PMID:26437932	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002013	PMID:23829229;OMIM:256810;PMID:23714749;PMID:18329934	PCS		15/30			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2012-10-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002098	PMID:16909392	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002495	PMID:24190800;PMID:22508010;PMID:28673863;PMID:34979697;PMID:26437932	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001284	PMID:22508010;PMID:16909392;PMID:22824774;PMID:26437932;PMID:18329934	PCS		8/9			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002490	PMID:23829229	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0034323	PMID:23714749	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0100560	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0011900	PMID:28209105	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0034295	PMID:20074988	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000869	PMID:24190800	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0100559	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000508	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0030890	PMID:18695062;PMID:24190800;PMID:31664948;PMID:22508010;PMID:22824774;PMID:28673863;PMID:34035203	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0009830	PMID:20074988;PMID:16909392;PMID:23714749	PCS		8/29			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0008347	PMID:16909392;PMID:23714749	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002922	PMID:22508010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002403	PMID:28673863;PMID:34979697	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003458	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003676	PMID:16909392	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002188	PMID:18695062;PMID:27536553	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001256	PMID:34023347;PMID:24190800;PMID:22508010;PMID:26437932	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002342	PMID:34023347;PMID:24190800;PMID:22508010;PMID:26437932	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001250	PMID:18695062;PMID:31664948;PMID:16909392;PMID:34035203;PMID:18329934	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003155	PMID:31664948;PMID:28209105;PMID:22824774;PMID:24894789	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0012707	PMID:18695062	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001252	PMID:18695062;PMID:23829229;PMID:27536553;PMID:22508010;PMID:16909392;PMID:22824774;PMID:23714749;PMID:24894789;PMID:34035203	PCS		21/33			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2014-11-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001251	OMIM:256810	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002460	PMID:22508010;PMID:16909392	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003270	PMID:16909392;PMID:25129007	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0012389	PMID:34979697	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0009141	PMID:20074988;PMID:22824774;PMID:23714749;PMID:18329934	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000716	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0011463	PMID:34023347;PMID:27536553;PMID:23714749;PMID:34035203	PCS		4/23			C	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0011462	PMID:24190800;PMID:34979697;PMID:22964873	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0009027	PMID:22508010;PMID:34979697	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001405	PMID:18695062	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001404	PMID:16909392	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006554	OMIM:256810;PMID:34023347	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000559	PMID:16909392	PCS		2/3			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001406	PMID:29318572;PMID:28209105;PMID:25129007	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002579	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001763	PMID:34979697	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001249	PMID:34979697	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000952	PMID:18695062;PMID:29318572;PMID:31664948;PMID:16909392;PMID:25129007;PMID:23714749;PMID:24894789;PMID:18329934	PCS		23/35			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001403	PMID:28209105;PMID:16909392;PMID:24894789	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000556	PMID:18329934	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003546	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003700	PMID:22824774	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001765	PMID:34979697	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001402	PMID:16909392	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001265	PMID:29318572;PMID:23829229;PMID:16909392;PMID:28673863	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003323	PMID:16909392	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003202	PMID:16909392	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001300	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003200	PMID:18695062;PMID:22508010;PMID:28673863;PMID:34979697	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001541	PMID:23829229;PMID:16909392;PMID:25129007;PMID:24894789	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001662	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002354	PMID:24190800	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0011968	PMID:23829229;PMID:22824774;PMID:23714749	PCS		7/19			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006937	PMID:24190800;PMID:22508010;PMID:16909392;PMID:28673863;PMID:26437932;PMID:34979697	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001260	PMID:28673863	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001263	PMID:33486010;PMID:20074988;PMID:24190800;PMID:27536553;PMID:22508010;PMID:26437932;PMID:34035203;PMID:31664948;PMID:16909392;PMID:34979697;PMID:28673863;PMID:23714749;PMID:18329934	PCS		19/44			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002194	PMID:24190800;PMID:34979697;PMID:34035203	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0030948	PMID:18695062;PMID:23829229;PMID:28209105;PMID:16909392;PMID:26437932;PMID:24894789	PCS		7/12			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003281	PMID:23829229;PMID:24894789	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002908	PMID:18695062;PMID:29318572;PMID:28209105;PMID:22824774;PMID:16909392;PMID:28673863;PMID:34979697;PMID:34035203	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0008163	PMID:23714749	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002904	PMID:31664948	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0040189	PMID:22824774	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002505	PMID:16909392	PCS		2/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002747	PMID:28209105	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003438	PMID:24190800;PMID:28673863;PMID:26437932	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0005978	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001414	PMID:18695062;PMID:29318572;OMIM:256810;PMID:28209105;PMID:24894789	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001413	PMID:16909392	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003376	PMID:24190800	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003256	PMID:23829229;PMID:25129007;PMID:23714749	PCS		4/19			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0012804	PMID:16909392	PCS		2/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003493	PMID:34979697	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0010864	PMID:34023347;PMID:24190800;PMID:22508010;PMID:26437932	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0008151	PMID:18695062;PMID:29318572;PMID:24190800;PMID:31664948;PMID:28209105;PMID:16909392;PMID:22824774;PMID:34979697;PMID:28673863;PMID:24894789;PMID:34035203	PCS		13/15			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0007460	OMIM:256810	TAS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001508	PMID:23829229;PMID:20074988;PMID:28209105;PMID:22824774;PMID:34035203;PMID:24894789;PMID:18695062;PMID:29318572;PMID:31664948;PMID:16909392;PMID:34979697;PMID:23714749;PMID:18329934	PCS		25/46			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0007340	PMID:16909392;PMID:34979697;PMID:26437932;PMID:22964873	PCS		8/10			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0031374	PMID:24190800;PMID:34979697	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006254	PMID:18695062;PMID:31664948;PMID:28209105;PMID:26437932	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001988	PMID:16909392	PCS		2/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0009005	PMID:34979697	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001987	PMID:18695062;PMID:24190800;PMID:22824774;PMID:25129007;PMID:34979697	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003648	PMID:23829229	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002317	PMID:26437932	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0007588	PMID:22824774	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0008954	PMID:24190800;PMID:22508010;PMID:26437932	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001744	PMID:29318572;PMID:24190800;PMID:25129007;PMID:34979697;PMID:28673863;PMID:24894789	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003128	PMID:18695062;PMID:23829229;PMID:20074988;PMID:24190800;PMID:16909392;PMID:18329934;PMID:34035203	PCS		21/23			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003645	PMID:29318572;PMID:31664948;PMID:28209105;PMID:22824774;PMID:24894789	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0008936	PMID:29318572;PMID:23829229	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000431	PMID:18695062;PMID:22824774	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002299	PMID:22824774	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003542	PMID:28673863;PMID:26437932	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001761	PMID:22508010	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002572	PMID:20074988;PMID:27536553;PMID:22824774	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001081	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0002172	PMID:28673863	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0003380	PMID:16909392;PMID:34979697	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26];HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0009072	PMID:34979697	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000829	PMID:20074988;PMID:23714749	PCS		3/24			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0009073	PMID:22964873	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0032230	PMID:34979697	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0031141	PMID:25129007;PMID:34035203	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001518	PMID:18695062;PMID:23829229;PMID:27536553;PMID:28209105;PMID:22824774	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0006121	OMIM:256810	TAS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0007178	PMID:27536553	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000821	PMID:23714749	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0001510	PMID:16909392	PCS		3/6			P	HPO:probinson[2022-12-13]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000666	PMID:27536553	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0000787	PMID:22824774	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:256810	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)		HP:0008944	PMID:24190800;PMID:22508010;PMID:16909392;PMID:26437932;PMID:34979697	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-10-26]
OMIM:613163	GABA-transaminase deficiency		HP:0001254	PMID:10407778	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0025430	PMID:10407778	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0000098	PMID:10407778	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0000494	PMID:10407778	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0001321	PMID:10407778	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0001250	PMID:10407778	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0011968	PMID:10407778	PCS		2/2			P	HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0001252	PMID:10407778	PCS		2/2			P	HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0001263	PMID:10407778	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0001274	PMID:10407778	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0010851	PMID:10407778	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0007291	PMID:10407778	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0003819	PMID:10407778	PCS		2/2			C	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0000007	PMID:10407778	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0000278	PMID:10407778	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0002415	PMID:10407778	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0001347	PMID:10407778	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-23]
OMIM:613163	GABA-transaminase deficiency		HP:0003623	PMID:10407778	PCS		2/2			C	HPO:probinson[2023-02-23]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0003202	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0003621	PMID:8012387	PCS		3/10			C	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0003487	PMID:8012387	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001310	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001761	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001371	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001260	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0002064	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0003593	PMID:8012387	PCS		2/10			C	HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0002061	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0000639	PMID:8012387	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0007340	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001419	PMID:8012387	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0011463	PMID:8012387	PCS		5/10			C	HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001317	OMIM:312920	IEA					P	HPO:skoehler[2018-10-08]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0000648	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0002505	PMID:8012387	PCS		5/11			P	HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001258	PMID:8012387	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-13]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0002503	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001249	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0002314	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:312920	Spastic paraplegia 2, X-linked		HP:0001347	OMIM:312920	IEA					P	HPO:iea[2009-02-17]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0001265	PMID:29499166	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0003621	PMID:29499166	PCS					C	HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0003376	PMID:29499166	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0001761	PMID:29499166	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0003693	PMID:29499166	PCS					P	HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0003394	PMID:29499166	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0003581	PMID:29499166	PCS					C	HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0001284	PMID:29499166	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0002460	PMID:29499166	PCS					P	HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0007141	PMID:29499166	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0009027	PMID:29499166	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0006886	PMID:29499166	PCS					P	HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0000006	PMID:29499166	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-15]
OMIM:618036	Charcot-Marie-Tooth disease, axonal, type 2DD		HP:0003677	PMID:29499166	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001374	PMID:8298651	PCS		1/11			P	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0002023	PMID:14681828	PCS	HP:0003577	1/9			P	HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0002023	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001651	PMID:8298651	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0000085	PMID:14681828	PCS	HP:0003577	2/9			P	HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0011536	PMID:8298651	PCS		1/2			P	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0031348	PMID:8298651	PCS		3/11			P	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0012304	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0000316	OMIM:306955	TAS					P	HPO:skoehler[2015-12-30]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001800	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0000238	PMID:8298651;PMID:21465648	PCS		2/13			P	HPO:probinson[2022-02-24];HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001643	PMID:14681828	PCS	HP:0003577	1/9			P	HPO:iea[2009-02-17];HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001643	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0003305	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001642	PMID:8298651	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0002475	PMID:8298651;PMID:21465648	PCS		2/13			P	HPO:probinson[2022-02-24];HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0003363	PMID:8298651;PMID:14681828	PCS		11/13			P	HPO:probinson[2022-02-24];HPO:skoehler[2009-02-17];HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0011565	OMIM:306955	TAS					P	HPO:skoehler[2017-07-13]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0033379	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001419	PMID:14681828	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001539	PMID:14681828	PCS	HP:0003577	1/9			P	HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0000961	OMIM:306955	IEA					P	HPO:skoehler[2019-09-07]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0000369	PMID:14681828	PCS		2/9			P	HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001655	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001776	PMID:8298651;PMID:21465648	PCS		2/13			P	HPO:probinson[2022-02-24];HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0003577	PMID:8298651	PCS		11/11			C	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001674	PMID:8298651	PCS		1/11			P	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001750	PMID:8298651;PMID:14681828	PCS		3/20			P	HPO:probinson[2022-02-24];HPO:skoehler[2015-12-30];HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0002240	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0004383	PMID:21465648	PCS		2/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0010305	PMID:8298651	PCS		1/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001629	PMID:21465648;PMID:14681828	PCS		11/12			P	HP:probinson[2022-02-24];HPO:iea[2009-02-17];HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001508	OMIM:306955	TAS					P	HPO:skoehler[2015-12-30]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0012890	PMID:8298651	PCS		1/11			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0011560	PMID:8298651	PCS		2/11			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001669	PMID:8298651;PMID:14681828	PCS		6/11			P	HPO:probinson[2022-02-24];HPO:skoehler[2015-12-30];HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001746	PMID:8298651;PMID:14681828	PCS		7/12			P	HPO:probinson[2022-02-24];HPO:skoehler[2009-02-17];HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0006695	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001748	PMID:8298651	PCS		2/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0003026	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0002410	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001682	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001561	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001321	PMID:8298651	PCS		1/11			P	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001640	PMID:8298651	PCS		3/11			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0002098	OMIM:306955	IEA					P	HPO:skoehler[2019-09-07]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001680	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0005160	PMID:21465648	PCS		2/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0011861	PMID:8298651	PCS		1/2			P	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001719	PMID:14681828	PCS	HP:0003577	4/9			P	HP:probinson[2019-01-25]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001719	PMID:8298651	PCS		2/11			P	HPO:probinson[2022-02-24];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001719	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001718	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0011670	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0005912	PMID:8298651	PCS		1/11			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0001631	OMIM:306955	TAS					P	HPO:skoehler[2015-12-30]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0000105	PMID:21465648	PCS		1/2			P	HP:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0002247	PMID:8298651	PCS		1/11			P	HPO:probinson[2022-02-24]
OMIM:306955	Heterotaxy, visceral, 1, X-linked		HP:0000104	OMIM:306955	TAS					P	HPO:skoehler[2015-12-30]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0008936	PMID:33313762	PCS		1/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000483	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0002540	PMID:33313762	PCS		2/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000750	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000486	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0003487	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0031936	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000540	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0002395	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0001371	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0001260	PMID:33313762	PCS		3/3		HP:0012828	P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0200049	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000470	PMID:33313762	PCS		1/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0003593	PMID:33313762	PCS		3/3			C	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000639	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0006895	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0025336	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0002307	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0003429	PMID:33313762	PCS		3/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000543	PMID:33313762	PCS	HP:0011463	1/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0001763	PMID:33313762	PCS		1/3			P	HPO:probinson[2021-06-26];HPO:probinson[2022-12-03]
OMIM:619328	Leukodystrophy, hypomyelinating, 22		HP:0000006	PMID:33313762	PCS					I	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:105200	Amyloidosis, familial visceral		HP:0001396	OMIM:105200	TAS					P	HPO:probinson[2009-02-17]
OMIM:105200	Amyloidosis, familial visceral		HP:0000112	OMIM:105200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:105200	Amyloidosis, familial visceral		HP:0000100	PMID:8097946	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-06]
OMIM:105200	Amyloidosis, familial visceral		HP:0000790	OMIM:105200	TAS					P	HPO:probinson[2009-02-17]
OMIM:105200	Amyloidosis, familial visceral		HP:0003581	PMID:8097946	PCS		3/3			C	HPO:probinson[2024-03-06]
OMIM:105200	Amyloidosis, familial visceral		HP:0002240	OMIM:105200	TAS					P	HPO:probinson[2009-02-17]
OMIM:105200	Amyloidosis, familial visceral		HP:0000093	PMID:8113408	PCS					P	HPO:probinson[2009-02-17]
OMIM:105200	Amyloidosis, familial visceral		HP:0000969	PMID:8113408	PCS					P	HPO:skoehler[2010-06-20]
OMIM:105200	Amyloidosis, familial visceral		HP:0001917	PMID:8097946	PCS		3/3			P	HPO:probinson[2024-03-06]
OMIM:105200	Amyloidosis, familial visceral		HP:0000822	PMID:8113408	PCS					P	HPO:probinson[2009-02-17]
OMIM:105200	Amyloidosis, familial visceral		HP:0009830	PMID:8097946	PCS		0/3			P	HPO:probinson[2012-07-26];HPO:probinson[2024-03-06]
OMIM:105200	Amyloidosis, familial visceral		HP:0000988	OMIM:105200	TAS					P	HPO:skoehler[2010-06-20]
OMIM:105200	Amyloidosis, familial visceral		HP:0000006	PMID:8464497	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-06]
OMIM:105200	Amyloidosis, familial visceral		HP:0001744	OMIM:105200	TAS					P	HPO:probinson[2009-02-17]
OMIM:105200	Amyloidosis, familial visceral		HP:0003216	PMID:22693999	PCS					P	HPO:probinson[2009-02-17]
OMIM:603358	Gracile syndrome		HP:0001396	PMID:12215968	PCS	HP:0003623	19/20			P	HPO:probinson[2013-02-18]
OMIM:603358	Gracile syndrome		HP:0003355	PMID:12215968	PCS	HP:0003623	20/20			P	HPO:probinson[2013-02-18]
OMIM:603358	Gracile syndrome		HP:0003542	PMID:12215968	PCS	HP:0003623				P	HPO:probinson[2013-02-18]
OMIM:603358	Gracile syndrome		HP:0003452	PMID:12215968	PCS	HP:0003623				P	HPO:probinson[2013-02-18]
OMIM:603358	Gracile syndrome		HP:0000007	PMID:12215968	PCS					I	HPO:probinson[2020-06-27]
OMIM:603358	Gracile syndrome		HP:0004925	PMID:12215968	PCS	HP:0003623				P	HPO:probinson[2013-02-18]
OMIM:603358	Gracile syndrome		HP:0001319	PMID:12215968	PCS	HP:0003623	3/20			P	HPO:probinson[2013-02-18]
OMIM:603358	Gracile syndrome		HP:0003281	PMID:12215968	PCS	HP:0003623				P	HPO:probinson[2013-02-18]
OMIM:603358	Gracile syndrome		HP:0001511	PMID:12215968	PCS					P	HPO:probinson[2013-02-18]
OMIM:148300	Keratoconus 1		HP:0000483	OMIM:148300	IEA					P	HPO:iea[2009-02-17]
OMIM:148300	Keratoconus 1		HP:0000563	PMID:11978762	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:148300	Keratoconus 1		HP:0011462	OMIM:148300	TAS					C	HPO:skoehler[2012-10-17]
OMIM:148300	Keratoconus 1		HP:0000006	PMID:11978762	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2022-03-15]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000286	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001498	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000486	OMIM:610442	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0004322	PMID:27213289	PCS		9/9			P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001250	OMIM:610442	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001252	PMID:27213289	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001251	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001290	OMIM:610442	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000280	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000639	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0011220	PMID:27213289	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0012471	PMID:27213289	PCS					P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001007	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001249	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0020206	OMIM:610442	TAS					P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000252	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0002079	OMIM:610442	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001382	OMIM:610442	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000294	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0003085	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0012697	OMIM:610442	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000926	PMID:27213289	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000007	PMID:27213289	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0002868	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000248	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000445	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0003015	OMIM:610442	TAS					P	HPO:probinson[2015-03-21]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0002162	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0001270	PMID:27213289	PCS					P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0031367	PMID:27213289	PCS					P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0010585	PMID:27213289	PCS					P	HPO:probinson[2012-06-18];HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0100864	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0012650	PMID:27213289	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000414	PMID:27213289	PCS					P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0002119	OMIM:610442	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000179	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0003301	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0002059	PMID:27213289	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0003025	OMIM:610442	TAS					P	HPO:probinson[2015-03-21]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0002651	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0004233	PMID:27213289	PCS					P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0005121	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000470	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0005280	PMID:27213289	PCS					P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0003180	OMIM:610442	IEA					P	HPO:iea[2009-02-17]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0034295	PMID:27213289	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0010582	OMIM:610442	TAS					P	HPO:probinson[2012-06-18]
OMIM:610442	Spondyloepimetaphyseal dysplasia, Camera-Genevieve type		HP:0000664	PMID:27213289	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0002465	OMIM:606220	IEA					P	HPO:skoehler[2019-09-07]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000252	PMID:30481285	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000750	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000486	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000431	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0006979	PMID:30481285	PCS		1/8			P	HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0031936	PMID:30481285	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0004322	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0001382	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0001260	PMID:30481285	PCS		6/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0001263	PMID:30481285	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0001373	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0003593	PMID:30481285	PCS					C	HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000308	PMID:30481285	PCS		5/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0010044	PMID:30481285	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000718	PMID:30481285	PCS		1/8			P	HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000508	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000448	PMID:30481285	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000007	PMID:30481285	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000414	PMID:30481285	PCS		8/8			P	HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000218	PMID:30481285	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0000894	PMID:30481285	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-11]
OMIM:606220	Intellectual developmental disorder with short stature, facial anomalies, and speech defects		HP:0001249	PMID:30481285	PCS		8/8			P	HPO:probinson[2022-09-11]
OMIM:308950	Lesch-Nyhan phenotype with normal hgprt		HP:0001266	OMIM:308950	IEA					P	HPO:iea[2009-02-17]
OMIM:308950	Lesch-Nyhan phenotype with normal hgprt		HP:0001417	OMIM:308950	IEA					I	HPO:iea[2009-02-17]
OMIM:308950	Lesch-Nyhan phenotype with normal hgprt		HP:0001257	OMIM:308950	IEA					P	HPO:iea[2009-02-17]
OMIM:308950	Lesch-Nyhan phenotype with normal hgprt		HP:0001249	OMIM:308950	IEA					P	HPO:iea[2009-02-17]
OMIM:308950	Lesch-Nyhan phenotype with normal hgprt		HP:0000742	OMIM:308950	IEA					P	HPO:iea[2009-02-17]
OMIM:308950	Lesch-Nyhan phenotype with normal hgprt		HP:0002149	OMIM:308950	IEA					P	HPO:iea[2009-02-17]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000252	PMID:24204302	PCS		3/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0003577	PMID:25053765	PCS		3/3			C	HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0002650	PMID:24204302	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0004322	PMID:24204302	PCS		3/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0025383	PMID:24204302	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0001250	PMID:25053765	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0001382	PMID:24204302	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0002121	PMID:24204302	PCS		1/3			P	HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0001263	PMID:25053765	PCS		3/3			P	HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000470	PMID:24204302	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000294	PMID:24204302	PCS		1/3			P	HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0001270	PMID:25053765	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000819	PMID:24204302	PCS		3/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000939	PMID:24204302	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000825	PMID:25053765	PCS		3/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0011451	PMID:25053765	PCS	HP:0003577	3/3			P	HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0025515	PMID:25053765	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000007	PMID:24204302	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000823	PMID:25053765	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0001249	PMID:25053765;PMID:24204302	PCS		6/6			P	HPO:probinson[2022-09-08];HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:5000011	PMID:24204302	PCS		0/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000445	PMID:24204302	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:616033	Microcephaly, short stature, and impaired glucose metabolism 1		HP:0000786	PMID:25053765	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-09-08]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0002079	PMID:34077761	PCS					P	HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0002098	PMID:34077761	PCS		5/6			P	HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0001250	PMID:34077761	PCS		2/7			P	HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0002110	PMID:34077761	PCS					P	HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0001274	PMID:34077761	PCS					P	HPO:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0001339	PMID:34077761	PCS		7/7			P	HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0000007	PMID:34077761	PCS					I	HPO:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0000389	PMID:34077761	PCS					P	HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0002205	PMID:34077761	PCS		6/6			P	HPO:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0100750	PMID:34077761	PCS					P	HPO:probinson[2021-10-19];HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0031602	PMID:34077761	PCS					P	HPO:probinson[2021-10-19]
OMIM:619466	Ciliary dyskinesia, primary, 47, and lissencephaly		HP:0003623	PMID:34077761	PCS		7/7			C	HPO:probinson[2021-10-19]
OMIM:618778	Deafness, autosomal dominant 75		HP:0000375	PMID:31231791	PCS		0/4			P	HPO:probinson[2020-05-08];HPO:probinson[2024-03-16]
OMIM:618778	Deafness, autosomal dominant 75		HP:0000407	PMID:31231791	PCS	HP:0003581	4/4			P	HPO:probinson[2020-05-08]
OMIM:618778	Deafness, autosomal dominant 75		HP:0011462	PMID:31231791	PCS		2/2			C	HPO:probinson[2024-03-16]
OMIM:618778	Deafness, autosomal dominant 75		HP:0000006	PMID:31231791	PCS					I	HPO:probinson[2020-05-08];HPO:probinson[2020-05-08]
OMIM:614156	Hyperbiliverdinemia		HP:0001396	OMIM:614156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614156	Hyperbiliverdinemia		HP:0001410	OMIM:614156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614156	Hyperbiliverdinemia		HP:0034383	PMID:19580635	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:614156	Hyperbiliverdinemia		HP:0003584	PMID:19580635	PCS		1/1			C	HPO:probinson[2022-09-07]
OMIM:614156	Hyperbiliverdinemia		HP:0001081	OMIM:614156	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614156	Hyperbiliverdinemia		HP:0000007	OMIM:614156	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614156	Hyperbiliverdinemia		HP:0032003	PMID:19580635	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-07]
OMIM:614156	Hyperbiliverdinemia		HP:0000006	OMIM:614156	TAS					I	HPO:skoehler[2012-10-17]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0001156	OMIM:113310	IEA					P	HPO:skoehler[2015-01-19]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0006492	OMIM:113310	IEA					P	HPO:skoehler[2010-06-18]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0002990	OMIM:113310	TAS					P	HPO:probinson[2009-02-17]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0003828	OMIM:113310	TAS					M	HPO:skoehler[2017-07-13]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0001839	OMIM:113310	TAS					P	HPO:probinson[2009-02-17]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0003829	OMIM:113310	TAS					I	HPO:skoehler[2017-07-13]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0009803	OMIM:113310	IEA					P	HPO:probinson[2009-02-17]
OMIM:113310	Brachydactyly-Ectrodactyly with fibular aplasia or hypoplasia		HP:0000006	OMIM:113310	TAS					I	HPO:skoehler[2017-07-13]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0012133	PMID:20378560	PCS					P	HPO:probinson[2013-03-12]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0004322	OMIM:612527	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0001999	OMIM:612527	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0001896	PMID:20378560	PCS					P	HPO:probinson[2013-03-12]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0001972	PMID:20378560	PCS					P	HPO:probinson[2013-03-12]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0001631	OMIM:612527	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0001510	OMIM:612527	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0000006	PMID:20378560	PCS					I	HPO:probinson[2013-03-12]
OMIM:612527	Diamond-Blackfan anemia 4		HP:0001875	OMIM:612527	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0003621	PMID:18006477	PCS		1/8			C	HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0003596	PMID:18006477	PCS		3/8			C	HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0003584	PMID:18006477	PCS		1/8			C	HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0005144	OMIM:615248	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0005110	PMID:18006477	PCS		1/11			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0033755	PMID:18006477	PCS		8/10			P	HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0001639	OMIM:615248	TAS					P	HPO:skoehler[2015-07-05];HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0011462	PMID:18006477	PCS		3/8			C	HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0001635	PMID:18006477	PCS		5/11			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0001712	PMID:18006477	PCS		3/11			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0001653	PMID:18006477	PCS		1/11			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0000006	PMID:18006477	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-03]
OMIM:615248	Cardiomyopathy, dilated, 1KK		HP:0001644	PMID:18006477	PCS		11/11			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-07-03]
OMIM:232400	Glycogen storage disease III		HP:0003236	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0000233	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0004322	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0003077	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0003198	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0003693	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0000490	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0001395	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0000272	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0002240	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0011800	OMIM:232400	TAS					P	HPO:skoehler[2013-11-28]
OMIM:232400	Glycogen storage disease III		HP:6000616	PMID:10472540	PCS		4/4			P	HPO:probinson[2024-04-03]
OMIM:232400	Glycogen storage disease III		HP:0005280	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0000007	OMIM:232400	IEA					I	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0001943	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0001638	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0000219	OMIM:232400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:232400	Glycogen storage disease III		HP:0001714	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0001324	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0000455	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:232400	Glycogen storage disease III		HP:0002910	OMIM:232400	IEA					P	HPO:iea[2009-02-17]
OMIM:619472	VISS syndrome		HP:0011819	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0004322	PMID:33875846	IEA		2/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0005133	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002020	PMID:33875846	PCS		2/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000639	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0100802	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0010297	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000637	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000358	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000252	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0005302	PMID:34010604	PCS		4/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0004970	PMID:34010605	PCS		6/6			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000490	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0011003	PMID:34010604	PCS		7/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0007394	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002827	PMID:34010605	PCS		1/7		HP:0031796	P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000767	PMID:34010604;PMID:33875846;PMID:34010605	PCS		11/28			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000007	PMID:34010605	PCS					I	HPO:probinson[2021-10-10];HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002705	PMID:33875846	PCS		2/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000768	PMID:34010604;PMID:33875846	PCS		4/21			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000400	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000520	PMID:34010604	PCS		7/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0003237	PMID:34010604	PCS		3/3			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000248	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000369	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000126	PMID:34010604;PMID:33875846	PCS		6/21			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002028	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0005116	PMID:34010605	PCS		2/2			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0003577	PMID:34010605	PCS		7/7			C	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0003212	PMID:34010604	PCS		3/3			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002761	OMIM:619472	TAS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000185	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0005231	PMID:34010604	PCS		2/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001270	PMID:34010605	PCS		7/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0100310	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0012450	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0004938	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0004937	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000978	PMID:34010605	PCS		2/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000218	PMID:33875846;PMID:34010605	PCS		7/16			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0025116	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000974	PMID:34010604;PMID:33875846	PCS		9/21			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001667	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000973	PMID:33875846	PCS		2/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001166	PMID:34010604;PMID:34010605	PCS		12/19			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001561	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002015	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002650	PMID:34010604;PMID:34010605	PCS		12/19			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001047	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002376	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000193	PMID:34010604;PMID:33875846;PMID:34010605	PCS		5/28			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002099	PMID:34010604	PCS		4/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000592	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002097	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0031298	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002094	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002092	PMID:33875846	PCS		2/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0011587	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0033117	PMID:34010604	PCS		1/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001838	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002808	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0011595	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0012163	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001719	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000508	PMID:34010604;PMID:34010605	PCS		7/19			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002007	PMID:34010604;PMID:34010605	PCS		9/19			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0006687	PMID:34010605	PCS		2/2			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0004944	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000347	PMID:34010604;PMID:33875846	PCS		8/21			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0031869	PMID:34010604	PCS		7/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0010809	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001252	PMID:33875846;PMID:34010605	PCS		13/16			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0003270	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000316	PMID:34010604;PMID:33875846;PMID:34010605	PCS		13/28			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002616	PMID:34010604;PMID:34010605	PCS		17/19			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002857	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001643	PMID:33875846;PMID:34010605	PCS		5/16			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000158	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000278	PMID:34010605	PCS		6/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001763	PMID:34010605	PCS		5/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001249	PMID:34010604;PMID:34010605	PCS		9/19			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001007	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001385	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001382	PMID:34010604;PMID:33875846;PMID:34010605	PCS		26/37			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0011968	PMID:33875846	PCS		2/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001263	PMID:34010605	PCS		3/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001263	PMID:34010604	PCS		7/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001263	PMID:33875846	PCS	HP:0003581	6/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0010511	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001537	PMID:34010604;PMID:33875846;PMID:34010605	PCS		18/28			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000964	PMID:34010604	PCS		3/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0003316	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002107	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001655	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000541	PMID:34010604	PCS		2/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000023	PMID:34010604;PMID:34010605	PCS		6/19			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001596	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0100348	PMID:34010605	PCS		1/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0032061	PMID:34010604	PCS		4/5			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001629	PMID:34010604;PMID:33875846;PMID:34010605	PCS		9/28			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001508	PMID:33875846	PCS		5/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:4000067	PMID:34010604	PCS		2/12			P	HPO:probinson[2022-02-03]
OMIM:619472	VISS syndrome		HP:0000656	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000378	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0004459	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0410323	PMID:34010604	PCS		1/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001762	PMID:33875846;PMID:34010605	PCS		3/16			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0005280	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000308	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002608	PMID:34010604	PCS		2/12			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000426	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002209	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000821	PMID:33875846	PCS		1/9			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0000268	PMID:34010605	PCS		5/7			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001631	PMID:34010604;PMID:33875846;PMID:34010605	PCS		9/28			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0001634	PMID:34010604;PMID:33875846	PCS		3/21			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002720	PMID:34010604	PCS		3/4			P	HPO:probinson[2021-10-10]
OMIM:619472	VISS syndrome		HP:0002566	PMID:33875846	PCS		2/9			P	HPO:probinson[2021-10-10]
OMIM:606552	Episodic ataxia, type 4		HP:0000640	OMIM:606552	IEA					P	HPO:iea[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0000651	OMIM:606552	TAS					P	HPO:probinson[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0002321	OMIM:606552	IEA					P	HPO:iea[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0000617	OMIM:606552	IEA					P	HPO:iea[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0002131	OMIM:606552	IEA					P	HPO:iea[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0025312	OMIM:606552	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606552	Episodic ataxia, type 4		HP:0000360	OMIM:606552	TAS					P	HPO:probinson[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0002018	OMIM:606552	IEA					P	HPO:iea[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0001257	OMIM:606552	IEA					P	HPO:iea[2009-02-17]
OMIM:606552	Episodic ataxia, type 4		HP:0000006	OMIM:606552	IEA					I	HPO:iea[2009-02-17]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002421	PMID:27989324	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002540	PMID:27989324	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0000486	PMID:27989324	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002188	PMID:27989324	PCS		2/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001332	PMID:27989324	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001272	PMID:27989324	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001250	PMID:27989324	PCS		3/3		HP:0012837	P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002120	PMID:27989324	PCS		2/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001252	PMID:27989324	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0003593	PMID:27989324	PCS		1/3			C	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0032794	PMID:27989324	PCS		1/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0032653	PMID:27989324	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0033128	PMID:27989324	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001508	PMID:27989324	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0000817	PMID:27989324	PCS		1/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0025336	PMID:27989324	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0000510	PMID:27989324	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001324	PMID:27989324	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002019	PMID:27989324	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002558	PMID:27989324	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0003623	PMID:27989324	PCS		2/3			C	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001265	PMID:27989324	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0003202	PMID:27989324	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001344	PMID:27989324	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0003487	PMID:27989324	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0011968	PMID:27989324	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0001263	PMID:27989324	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002151	PMID:27989324	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0010818	PMID:27989324	PCS		2/3			P	HPO:probinson[2022-11-07];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0002490	PMID:27989324	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0100660	PMID:27989324	PCS		1/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0011097	PMID:27989324	PCS		1/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0007371	PMID:27989324	PCS		1/3			P	HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0007256	PMID:27989324	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0000007	PMID:27989324	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0200134	PMID:27989324	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:617339	Epileptic encephalopathy, early infantile, 51		HP:0007359	PMID:27989324	PCS		1/3			P	HPO:probinson[2022-11-07]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0001100	PMID:34323021;PMID:7874167	PCS		4/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0001022	OMIM:193510	TAS	HP:0003577				P	HPO:skoehler[2012-11-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0003577	PMID:7874167	PCS		8/8			C	HPO:probinson[2022-08-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0000431	OMIM:193510	IEA					P	HPO:iea[2009-02-17]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0000430	OMIM:193510	IEA					P	HPO:iea[2009-02-17]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0002211	PMID:7874167	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0000407	PMID:34323021;PMID:7874167	PCS	HP:0003577	12/14			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0007990	OMIM:193510	IEA					P	HPO:iea[2009-02-17]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0007443	OMIM:193510	IEA					P	HPO:iea[2009-02-17]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0007587	PMID:34323021	PCS		5/6			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0002216	PMID:7874167	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0000664	OMIM:193510	IEA					P	HPO:iea[2009-02-17]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0002227	OMIM:193510	PCS					P	HPO:iea[2012-03-01]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0000006	PMID:7874167	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-21]
OMIM:193510	Waardenburg syndrome, type 2A		HP:0002226	OMIM:193510	PCS					P	HPO:iea[2009-02-17]
OMIM:608219	Deafness, congenital neurosensory, autosomal recessive 38		HP:0000007	OMIM:608219	TAS					I	HPO:probinson[2009-02-17]
OMIM:608219	Deafness, congenital neurosensory, autosomal recessive 38		HP:0000399	OMIM:608219	TAS				HP:0012828	P	HPO:probinson[2009-02-17]
OMIM:264120	Prolactin deficiency with obesity and enlarged testes		HP:0000053	OMIM:264120	TAS					P	HPO:probinson[2009-02-17]
OMIM:264120	Prolactin deficiency with obesity and enlarged testes		HP:0008202	OMIM:264120	TAS					P	HPO:probinson[2009-02-17]
OMIM:264120	Prolactin deficiency with obesity and enlarged testes		HP:0000007	OMIM:264120	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:264120	Prolactin deficiency with obesity and enlarged testes		HP:0001513	OMIM:264120	TAS					P	HPO:probinson[2009-02-17]
OMIM:619314	Buratti-Harel syndrome		HP:0008947	PMID:32430360	PCS	HP:0003593	5/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000286	PMID:32430360	PCS		4/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000220	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0001792	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0003577	PMID:32430360	PCS		5/5			C	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000486	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0002020	PMID:32430360	PCS		4/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0001270	PMID:32430360	PCS		4/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0010055	PMID:32430360	PCS		2/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0008551	PMID:32430360	PCS		5/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000316	PMID:32430360	PCS		5/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0006532	PMID:32430360	PCS		2/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000218	PMID:32430360	PCS		2/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0001601	PMID:32430360	PCS		4/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000358	PMID:32430360	PCS		5/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000577	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000176	PMID:32430360	PCS		2/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000494	PMID:32430360	PCS		3/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000750	PMID:32430360	PCS		5/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000193	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0011304	PMID:32430360	PCS		2/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0012520	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000508	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0025325	PMID:32430360	PCS		5/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0004209	PMID:32430360	PCS		4/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000565	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0001631	PMID:32430360	PCS		1/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000047	PMID:32430360	PCS		1/3			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000006	PMID:32430360	PCS					I	HPO:probinson[2021-07-09];HPO:probinson[2022-12-03]
OMIM:619314	Buratti-Harel syndrome		HP:0000369	PMID:32430360	PCS		5/5			P	HPO:probinson[2021-07-09]
OMIM:619314	Buratti-Harel syndrome		HP:0000028	PMID:32430360	PCS		2/3			P	HPO:probinson[2021-07-09]
OMIM:236100	Holoprosencephaly 1		HP:0006988	OMIM:236100	IEA					P	HPO:iea[2009-02-17]
OMIM:236100	Holoprosencephaly 1		HP:0009914	OMIM:236100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:236100	Holoprosencephaly 1		HP:0004322	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0001750	OMIM:236100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:236100	Holoprosencephaly 1		HP:0001250	OMIM:236100	IEA					P	HPO:iea[2009-02-17]
OMIM:236100	Holoprosencephaly 1		HP:0000161	OMIM:236100	TAS					P	HPO:probinson[2024-03-29]
OMIM:236100	Holoprosencephaly 1		HP:0001274	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0012806	OMIM:236100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:236100	Holoprosencephaly 1		HP:0001290	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0030779	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0003829	OMIM:236100	TAS					I	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0001943	OMIM:236100	IEA					P	HPO:iea[2009-02-17]
OMIM:236100	Holoprosencephaly 1		HP:0000835	OMIM:236100	IEA					P	HPO:iea[2009-02-17]
OMIM:236100	Holoprosencephaly 1		HP:0000873	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0003745	OMIM:236100	TAS					I	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0001249	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0000252	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0000054	OMIM:236100	IEA					P	HPO:iea[2009-02-17]
OMIM:236100	Holoprosencephaly 1		HP:0009927	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0001321	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0001263	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0011800	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0009099	OMIM:236100	TAS					P	HPO:probinson[2024-03-29]
OMIM:236100	Holoprosencephaly 1		HP:0000007	OMIM:236100	IEA					I	HPO:iea[2009-02-17]
OMIM:236100	Holoprosencephaly 1		HP:0000601	OMIM:236100	IEA					P	HPO:iea[2009-02-17]
OMIM:236100	Holoprosencephaly 1		HP:0000568	OMIM:236100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0000006	OMIM:236100	TAS					I	HPO:skoehler[2017-07-13]
OMIM:236100	Holoprosencephaly 1		HP:0002006	OMIM:236100	IEA					P	HPO:iea[2009-02-17]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001298	OMIM:617301	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002267	OMIM:617301	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001276	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0003577	OMIM:617301	TAS					C	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002169	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000463	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000243	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001371	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0003273	OMIM:617301	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002816	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001845	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002119	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002878	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0025116	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000278	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002058	OMIM:617301	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0008936	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001188	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002015	OMIM:617301	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000252	OMIM:617301	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001762	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002079	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001382	OMIM:617301	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0001263	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0005280	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002827	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000508	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002804	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000007	OMIM:617301	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000648	OMIM:617301;PMID:27773429	PCS		12/20			P	HPO:skoehler[2017-07-13];HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000527	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000268	PMID:27773429	PCS					P	HP:probinson[2018-05-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002987	OMIM:617301	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0000369	PMID:27773429	PCS					P	HPO:skoehler[2017-07-13]
OMIM:617301	Glycine encephalopathy with normal serum glycine		HP:0002104	OMIM:617301	TAS				HP:0031796	P	HPO:skoehler[2017-07-13]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000365	PMID:22426308	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000343	PMID:22426308	PCS		2/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000463	OMIM:614608	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614608	Coffin-Siris syndrome 3		HP:0004322	PMID:22426308	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000023	PMID:22426308	PCS		2/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001250	PMID:22426308	PCS		2/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001252	PMID:22426308	PCS		4/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001273	PMID:22426308	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000280	PMID:22426308	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0002719	PMID:22426308	PCS		3/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0012471	PMID:22426308	PCS		4/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000998	OMIM:614608	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614608	Coffin-Siris syndrome 3		HP:0030680	OMIM:614608	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001305	PMID:22426308	PCS		0/2			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001627	OMIM:614608	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000218	PMID:22426308	PCS		4/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000158	PMID:22426308	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000696	PMID:22426308	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001007	PMID:22426308	PCS		3/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001249	OMIM:614608	TAS					P	HPO:probinson[2013-08-10]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000154	PMID:22426308	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000252	PMID:22426308	PCS		2/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000175	PMID:22426308	PCS		2/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0002650	PMID:22426308	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000574	PMID:22426308	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001321	PMID:22426308	PCS		2/3			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0002750	PMID:22426308	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0011968	PMID:22426308	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001382	PMID:22426308	PCS		2/3			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0002033	PMID:22426308	PCS		4/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001263	PMID:22426308	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0025195	PMID:22426308	PCS		1/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0005280	PMID:22426308	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000508	PMID:22426308	PCS		3/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0002209	PMID:22426308	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001537	PMID:22426308	PCS		0/4			P	HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000527	PMID:22426308	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000505	PMID:22426308	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0001511	PMID:22426308	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000006	PMID:22426308	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0000445	PMID:22426308	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:614608	Coffin-Siris syndrome 3		HP:0004227	PMID:22426308	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0010529	PMID:23065719	PCS					P	HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000486	OMIM:615516	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000189	OMIM:615516	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000750	PMID:23065719	PCS		7/7			P	HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0031936	PMID:23065719	PCS		7/7			P	HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0001250	OMIM:615516	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0002373	PMID:23065719	PCS		2/7			P	HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0001263	PMID:23065719	PCS		7/7			P	HPO:skoehler[2014-01-28];HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0003593	OMIM:615516	TAS					C	HPO:skoehler[2014-01-28]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0001290	OMIM:615516	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0031987	OMIM:615516	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0100023	PMID:23065719	PCS					P	HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000718	PMID:23065719	PCS					P	HPO:skoehler[2014-01-28];HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000729	PMID:23065719	PCS		6/7			P	HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000635	OMIM:615516	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000007	PMID:23065719	PCS					I	HPO:skoehler[2014-01-28];HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0002317	PMID:23065719	PCS		6/7			P	HPO:skoehler[2014-01-28];HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0001319	PMID:23065719	PCS	HP:0003623	4/7			P	HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0001852	OMIM:615516	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0001357	OMIM:615516	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000752	OMIM:615516	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000303	OMIM:615516	TAS					P	HPO:skoehler[2014-07-11]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0001249	PMID:23065719	PCS		7/7			P	HPO:skoehler[2014-01-28];HP:probinson[2019-04-20]
OMIM:615516	Intellectual developmental disorder, autosomal recessive 38		HP:0000742	PMID:23065719	PCS		4/7			P	HPO:skoehler[2014-01-28];HP:probinson[2019-04-20]
OMIM:615270	Hypogonadotropic hypogonadism 20 with or without anosmia		HP:0000939	OMIM:615270	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:615270	Hypogonadotropic hypogonadism 20 with or without anosmia		HP:0000938	PMID:23643382	PCS		2/3			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-09-21]
OMIM:615270	Hypogonadotropic hypogonadism 20 with or without anosmia		HP:0000458	PMID:23643382	PCS		2/3			P	HPO:probinson[2022-09-21]
OMIM:615270	Hypogonadotropic hypogonadism 20 with or without anosmia		HP:0000823	OMIM:615270	TAS					P	HPO:skoehler[2015-01-21]
OMIM:615270	Hypogonadotropic hypogonadism 20 with or without anosmia		HP:0000135	OMIM:615270	IEA					P	HPO:skoehler[2015-01-21]
OMIM:615270	Hypogonadotropic hypogonadism 20 with or without anosmia		HP:0000006	OMIM:615270	TAS					I	HPO:skoehler[2015-12-30]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000709	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0002015	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0001288	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000639	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000726	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000519	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000618	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000712	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0002072	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000751	OMIM:607674	IEA					P	HPO:iea[2009-02-17]
OMIM:607674	Cataract, congenital, with mental impairment and dentate gyrus atrophy		HP:0000006	OMIM:607674	IEA					I	HPO:iea[2009-02-17]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0025012	PMID:26063658	PCS		7/8			P	HPO:probinson[2017-11-11];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0001297	PMID:26063658	PCS		6/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0003596	PMID:26063658	PCS		3/8			C	HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0001288	PMID:26063658	PCS		6/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0001250	PMID:26063658	PCS		1/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0003584	PMID:26063658	PCS		5/8			C	HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0032325	PMID:26063658	PCS		10/11			P	HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0100543	PMID:26063658	PCS		5/10			P	HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0012520	PMID:26063658	PCS					P	HPO:probinson[2017-06-20]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0000726	PMID:26063658	PCS		1/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0030890	PMID:26063658	PCS		11/11			P	HPO:probinson[2017-06-20];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0000822	PMID:26063658	PCS		5/11			P	HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0007236	PMID:26063658	PCS					P	HPO:probinson[2017-06-20]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0002315	PMID:26063658	PCS		2/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0002326	PMID:26063658	PCS		6/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-24]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0001268	PMID:26063658	PCS					P	HPO:probinson[2017-06-20]
OMIM:616779	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2		HP:0000006	PMID:26063658	PCS					I	HPO:probinson[2017-06-20]
OMIM:608553	Leber congenital amaurosis 9		HP:0007737	PMID:22842231	PCS		1/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0007814	PMID:22842231	PCS		4/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000662	PMID:22842230;PMID:22842231	PCS		2/18			P	HPO:probinson[2022-05-29];HPO:skoehler[2012-11-18];HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000563	PMID:22842230	PCS		1/8			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000540	PMID:22842230	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0003593	PMID:22842231	PCS		8/9			C	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000639	PMID:22842230;PMID:22842231	PCS		12/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0011463	PMID:22842231	PCS		1/9			C	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0032286	PMID:22842231	PCS		7/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000613	OMIM:608553	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:608553	Leber congenital amaurosis 9		HP:0007663	PMID:22842230;PMID:22842231	PCS		27/27			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0007401	PMID:22842231	PCS		5/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0007843	OMIM:608553;PMID:22842231	PCS		16/21			P	HPO:probinson[2022-05-29];HPO:skoehler[2012-10-17]
OMIM:608553	Leber congenital amaurosis 9		HP:0007988	PMID:22842231	PCS		1/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000550	PMID:22842231	PCS		2/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000551	PMID:22842231	PCS		1/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0001483	PMID:22842231	PCS		1/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0032123	PMID:22842231	PCS		1/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0032027	PMID:22842230	PCS		8/8			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000007	PMID:22842230	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000648	OMIM:608553	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608553	Leber congenital amaurosis 9		HP:0200056	PMID:22842231	PCS		1/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0000543	OMIM:608553;PMID:22842231	PCS		12/21			P	HPO:probinson[2022-05-29];HPO:skoehler[2012-10-17]
OMIM:608553	Leber congenital amaurosis 9		HP:0000666	PMID:22842231	PCS		1/11			P	HPO:probinson[2022-05-29]
OMIM:608553	Leber congenital amaurosis 9		HP:0001116	PMID:22842230;PMID:22842231	PCS		19/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002982	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001177	PMID:20512146	PCS		2/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000286	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001770	PMID:20512146	PCS		7/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0004322	PMID:20512146	PCS		2/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001252	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001290	OMIM:277170	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000639	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0011340	PMID:20512146	PCS		2/10			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000316	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0009466	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002419	PMID:20512146	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000878	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001841	PMID:20512146	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0006159	PMID:20512146	PCS		6/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002139	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000358	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001249	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000175	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002990	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001263	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0011802	PMID:20512146	PCS		3/10			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0100259	OMIM:277170	TAS					P	HPO:skoehler[2014-11-26]
OMIM:277170	Orofaciodigital syndrome VI		HP:0006145	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000007	PMID:20512146	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000405	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000565	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000369	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000204	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002444	PMID:20512146	PCS		5/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0003577	PMID:20512146	PCS		12/12			C	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001156	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0003097	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001274	PMID:20512146	PCS		2/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0004383	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000180	PMID:20512146	PCS		3/10			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002280	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001508	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0100702	PMID:20512146	PCS		2/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000218	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0030084	OMIM:277170	TAS					P	HPO:skoehler[2014-09-21]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002436	PMID:20512146	PCS		2/12			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000455	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000110	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001320	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000199	OMIM:277170	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001162	PMID:20512146	PCS		7/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002132	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0001680	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0032388	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000191	PMID:20512146	PCS		4/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0002126	PMID:20512146	PCS		1/12			P	HPO:probinson[2022-10-12]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000347	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:277170	Orofaciodigital syndrome VI		HP:0000104	OMIM:277170	IEA					P	HPO:iea[2009-02-17]
OMIM:613615	Senior-Loken syndrome 7		HP:0000090	PMID:20835237	PCS		20/20			P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:613615	Senior-Loken syndrome 7		HP:0000007	PMID:20835237	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-07-20]
OMIM:613615	Senior-Loken syndrome 7		HP:0000546	PMID:20835237	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2020-07-20]
OMIM:604369	Salla disease		HP:0000750	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0002540	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0002684	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001250	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001260	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001252	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001263	OMIM:604369	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604369	Salla disease		HP:0001251	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001290	OMIM:604369	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604369	Salla disease		HP:0000639	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001939	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001922	OMIM:604369	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604369	Salla disease		HP:0000007	OMIM:604369	IEA					I	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001257	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001510	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0002305	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:604369	Salla disease		HP:0001249	OMIM:604369	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604369	Salla disease		HP:0000577	OMIM:604369	IEA					P	HPO:iea[2009-02-17]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000365	PMID:31239556	PCS		10/42			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001212	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000486	PMID:23746550	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-19]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001332	PMID:31239556	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0004322	PMID:23746550	PCS		1/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-06-19]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0008807	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002020	PMID:31239556	PCS		4/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0033725	PMID:31239556	PCS		1/26			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000637	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0009623	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001169	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000358	PMID:31239556;PMID:23746550	PCS		2/50			P	HPO:probinson[2023-02-11];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002553	PMID:31239556	PCS		3/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000494	PMID:31239556	PCS		3/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000252	PMID:31239556;PMID:23746550	PCS		21/45			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0011800	PMID:31239556	PCS		3/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001182	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0006101	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000527	PMID:31239556;PMID:23746550	PCS		6/50			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000400	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000006	PMID:23746550	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000248	PMID:31239556	PCS		4/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000369	PMID:31239556;PMID:23746550	PCS		3/50			P	HPO:probinson[2023-02-11];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001276	PMID:31239556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000341	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0003577	PMID:23746550	PCS		4/4			C	HPO:probinson[2022-06-19];HPO:probinson[2022-06-19]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000582	PMID:31239556	PCS		5/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000343	PMID:31239556;PMID:23746550	PCS		7/50			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000463	PMID:31239556	PCS		6/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001272	PMID:31239556	PCS		1/25			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000581	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000739	PMID:31239556	PCS		4/45			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0100702	PMID:31239556	PCS		4/25			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0012450	PMID:31239556	PCS		7/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000733	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0006970	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000219	PMID:31239556	PCS		13/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002119	PMID:31239556;PMID:23746550	PCS		6/29			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000455	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0011081	PMID:23746550	PCS		1/4			P	HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000336	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000750	PMID:31239556	PCS		31/41			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002650	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000233	PMID:31239556;PMID:23746550	PCS		9/9			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000194	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000592	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0010818	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001680	PMID:23746550	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0025190	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002808	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000508	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000348	PMID:31239556;PMID:23746550	PCS		2/50			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0007018	PMID:31239556	PCS		4/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000347	PMID:31239556	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001831	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000286	PMID:31239556;PMID:23746550	PCS		8/50			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001770	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000160	PMID:31239556;PMID:23746550	PCS		7/50			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001252	PMID:31239556;PMID:23746550	PCS		22/39			P	HPO:skoehler[2014-11-26];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001251	PMID:31239556	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002064	PMID:31239556	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000280	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0045075	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000716	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000718	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0011220	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000316	PMID:31239556;PMID:23746550	PCS		6/50			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000954	PMID:31239556;PMID:23746550	PCS		5/50			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001769	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002857	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001643	PMID:23746550	PCS		1/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001763	PMID:31239556	PCS		3/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001249	PMID:31239556;PMID:23746550	PCS		56/56			P	HPO:skoehler[2014-06-24];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000175	PMID:23746550	PCS		1/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001385	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000574	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000331	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0011968	PMID:31239556;PMID:23746550	PCS		35/47			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001382	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001263	PMID:31239556;PMID:23746550	PCS		50/50			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0012810	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0012385	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000729	PMID:31239556;PMID:23746550	PCS		10/50			P	ORCID:0000-0002-0736-9199[2024-05-10];HPO:skoehler[2014-04-04];HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000722	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000601	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000960	PMID:23746550	PCS		1/4			P	HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000322	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000325	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000540	PMID:23746550	PCS		3/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002162	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000939	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001508	PMID:31239556	PCS		22/43			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002719	PMID:31239556;PMID:23746550	PCS		19/45			P	HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001629	PMID:31239556	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000938	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0008551	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0030043	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000656	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0009765	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000378	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000411	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0005326	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000275	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000396	PMID:31239556	PCS		3/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0002059	PMID:31239556	PCS		1/25			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001762	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000431	PMID:31239556	PCS		3/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0031936	PMID:31239556	PCS		22/40			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000276	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001761	PMID:31239556	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0045025	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0011822	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0005280	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000308	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000426	PMID:31239556	PCS		2/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000307	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0200055	PMID:31239556	PCS		1/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0001631	PMID:31239556;PMID:23746550	PCS		7/10			P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04];ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000028	PMID:23746550	PCS		2/3	MALE		P	HPO:skoehler[2013-11-18];HPO:probinson[2019-09-04]
OMIM:615502	Intellectual developmental disorder, autosomal dominant 21		HP:0000303	PMID:31239556	PCS		5/46			P	ORCID:0000-0002-0736-9199[2024-05-10]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0007759	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0001058	OMIM:256800	TAS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0002164	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0012804	OMIM:256800	TAS					P	HPO:skoehler[2015-01-20]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0003593	OMIM:256800	IEA					C	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0012332	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0100725	OMIM:256800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0007460	OMIM:256800	TAS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0007021	OMIM:256800;PMID:8696348	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-10]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000712	OMIM:256800	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0002715	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000559	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000752	OMIM:256800	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0005307	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0007249	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0001249	PMID:8696348	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-10]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0002754	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000495	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000970	PMID:8696348	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-10]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000491	OMIM:256800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0001263	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0006121	OMIM:256800	IEA					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0002209	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0001954	OMIM:256800;PMID:8696348	PCS		14/14		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-10]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000007	PMID:8696348	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-10]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0002821	OMIM:256800	IEA					P	HPO:iea[2009-02-17]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0008404	OMIM:256800	TAS					P	HPO:skoehler[2013-05-03]
OMIM:256800	Insensitivity to pain, congenital, with anhidrosis		HP:0000742	PMID:8696348	PCS		4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-10]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0001254	PMID:21944046	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0003593	PMID:22077971;PMID:21944046	PCS		11/14			C	HPO:probinson[2022-11-23];HPO:probinson[2022-11-23];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0012402	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0001508	PMID:22077971;PMID:21944046;PMID:24462778	PCS		17/21			P	HPO:probinson[2022-11-23];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0011463	PMID:24462778	PCS		1/1			C	HPO:probinson[2022-11-23];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0008972	PMID:21944046	PCS		3/3			P	HPO:skoehler[2013-05-29];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0410309	PMID:22077971	PCS		10/10			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002878	PMID:21944046	PCS		4/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0003648	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0008314	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0001324	PMID:21944046	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0001522	PMID:21944046	PCS		1/4			C	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0003108	PMID:22077971;PMID:24462778	PCS		8/8			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0004911	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0003128	PMID:21944046	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0003623	PMID:21944046	PCS		3/4			C	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0008936	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002179	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0033418	PMID:21944046	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0007209	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002376	PMID:22077971	PCS		4/10			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0011968	PMID:21944046;PMID:24462778	PCS		4/4			P	HPO:probinson[2022-11-23];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002154	PMID:22077971;PMID:21944046;PMID:24462778	PCS		10/12			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002352	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0001263	PMID:22077971;PMID:21944046	PCS		4/11			P	HPO:probinson[2022-11-23];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002151	PMID:22077971;PMID:24462778	PCS		11/11			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0001285	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002490	PMID:22077971	PCS		4/4			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002092	PMID:22077971	PCS		7/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002093	PMID:21944046	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0002071	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0500230	PMID:22077971;PMID:21944046	PCS		8/8			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0033044	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0000007	PMID:21944046	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0003811	PMID:21944046	PCS		3/4			C	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0007359	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:605711	Multiple mitochondrial dysfunctions syndrome 1		HP:0001336	PMID:24462778	PCS		1/1			P	HPO:probinson[2022-11-23]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0008936	PMID:33239752	PCS		6/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0002069	PMID:33239752	PCS		6/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0000750	PMID:33239752	PCS		10/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0031936	PMID:33239752	PCS		12/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0002121	PMID:33239752	PCS		2/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0001260	PMID:33239752	PCS		3/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0003593	PMID:33239752	PCS		12/12			C	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0033051	PMID:33239752	PCS		1/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0011172	PMID:33239752	PCS		1/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0000518	PMID:33239752	PCS		12/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0011153	PMID:33239752	PCS		2/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0012450	PMID:33239752	PCS		5/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0000256	PMID:33239752	PCS		2/12			P	HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0000006	PMID:33239752	PCS					I	HPO:probinson[2021-07-01];HPO:probinson[2021-07-01]
OMIM:619338	Cataracts, spastic paraparesis, and speech delay		HP:0002313	PMID:33239752	PCS		12/12			P	HPO:probinson[2021-07-01]
OMIM:617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0007957	PMID:11403040	PCS					P	HPO:probinson[2017-06-16]
OMIM:617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0011490	PMID:11403040	PCS					P	HPO:probinson[2017-06-16]
OMIM:617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0011496	PMID:11403040	PCS					P	HPO:probinson[2017-06-16]
OMIM:617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0001087	PMID:11403040	PCS					P	HPO:probinson[2017-06-16]
OMIM:617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0011484	PMID:11403040	PCS					P	HPO:probinson[2017-06-16]
OMIM:617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0000007	PMID:27839872	PCS					I	HPO:probinson[2017-06-16]
OMIM:600669	Epilepsy, idiopathic generalized		HP:0002069	OMIM:600669	TAS					P	HPO:skoehler[2010-06-18]
OMIM:600669	Epilepsy, idiopathic generalized		HP:0010849	OMIM:600669	TAS					P	HPO:probinson[2009-02-17]
OMIM:600669	Epilepsy, idiopathic generalized		HP:0002123	OMIM:600669	TAS					P	HPO:probinson[2009-02-17]
OMIM:600669	Epilepsy, idiopathic generalized		HP:0002121	OMIM:600669	TAS					P	HPO:probinson[2009-02-17]
OMIM:600669	Epilepsy, idiopathic generalized		HP:0000006	OMIM:600669	TAS					I	HPO:probinson[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0003477	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0003676	PMID:8960746	PCS					C	HPO:skoehler[2012-10-12];HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000365	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001250	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001251	PMID:8960746	PCS		2/4			P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000639	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0007841	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001324	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002019	PMID:8960746	PCS		2/4			P	HPO:skoehler[2012-10-12];HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001265	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000651	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002078	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001260	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002070	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0011003	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000726	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000407	PMID:8960746	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0012185	OMIM:105210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0004926	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0008765	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000802	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001257	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000006	PMID:8960746	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001337	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001271	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000020	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0010544	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002080	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0012332	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000738	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0010550	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000739	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002315	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001269	OMIM:105210	IEA					P	HPO:skoehler[2010-06-20]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002313	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001347	PMID:8960746	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002014	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001289	PMID:8960746	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001640	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002572	PMID:8960746	PCS		2/4			P	HPO:probinson[2023-05-09];HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0003581	PMID:8960746	PCS		4/4			C	HPO:iea[2009-02-17];HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0011468	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0100598	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0011034	PMID:8960746	PCS		4/4			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000508	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0009830	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0007256	PMID:8960746	PCS		2/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0001638	OMIM:105210	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002922	PMID:8960746	PCS		4/4			P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000505	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002403	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0000666	PMID:8960746	PCS		1/4			P	HPO:probinson[2023-05-09]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0002401	OMIM:105210	IEA					P	HPO:iea[2009-02-17]
OMIM:105210	Amyloidosis, hereditary, transthyretin-related		HP:0032070	OMIM:105210	IEA					P	HPO:skoehler[2019-09-07]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0007957	PMID:21907015	PCS		11/11			P	HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0003577	PMID:21907015	PCS					C	HPO:probinson[2022-10-13];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0007906	PMID:21907015	PCS		3/7			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0000482	PMID:21907015	PCS		8/11			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0000518	PMID:21907015	PCS		7/7			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0011483	PMID:21907015	PCS		3/7			P	HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0000007	PMID:21907015	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0000557	PMID:21907015	PCS		3/11			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0000568	PMID:21907015	PCS		0/7			P	HPO:skoehler[2014-08-03];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0000612	PMID:21907015	PCS		0/7			P	HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0007663	PMID:21907015	PCS		11/11			P	HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0000647	PMID:21907015	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0007700	PMID:21907015	PCS					P	HPO:skoehler[2014-08-03];HPO:probinson[2022-10-13]
OMIM:269400	Corneal opacification with other ocular anomalies		HP:0003623	PMID:21907015	PCS					C	HPO:probinson[2022-10-13]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000044	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001332	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001272	PMID:30584594	PCS	HP:0011463	2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0003593	PMID:30584594	PCS		2/2			C	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001251	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000639	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001508	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0008872	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001946	PMID:30584594	PCS		1/2		HP:0033184	P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0025336	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001268	PMID:30584594	PCS		1/1			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000252	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001344	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000750	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0002273	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0100660	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0007371	PMID:30584594	PCS	HP:0011463	2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0033044	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000668	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000007	PMID:30584594	PCS					I	HPO:probinson[2021-07-03];HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000648	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001510	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0002305	PMID:30584594	PCS		1/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0000028	PMID:30584594	PCS		2/2			P	HPO:probinson[2021-07-03]
OMIM:619310	Leukodystrophy, hypomyelinating, 21		HP:0001259	PMID:30584594	PCS	HP:0003621	1/2		HP:0025334	P	HPO:probinson[2021-07-03]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0003774	OMIM:308940	TAS		3/4			P	HPO:skoehler[2012-11-21]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0000365	PMID:9915944	PCS		1/4			P	HPO:probinson[2023-03-13]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0000083	PMID:9915944	PCS	HP:0003581	4/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-03-13]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0030034	OMIM:308940	TAS					P	HPO:skoehler[2014-09-21]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0012211	OMIM:308940	IEA					P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0000518	OMIM:308940	IEA		3/4			P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0001508	OMIM:308940	IEA					P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0025710	PMID:9915944	PCS		1/4			C	HPO:probinson[2023-03-13]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0002019	OMIM:308940	TAS		1/4			P	HPO:skoehler[2012-10-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0006756	OMIM:308940	IEA					P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0002015	OMIM:308940	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0003621	PMID:9915944	PCS		3/4			C	HPO:probinson[2023-03-13];HPO:probinson[2023-03-13]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0000112	OMIM:308940	TAS					P	HPO:skoehler[2012-11-21]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0002013	OMIM:308940	IEA					P	HPO:skoehler[2010-06-20]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0000790	OMIM:308940	IEA		1/4			P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0001142	OMIM:308940	IEA		1/4			P	HPO:skoehler[2010-06-20]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0011501	OMIM:308940	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0002094	OMIM:308940	IEA					P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0000093	OMIM:308940	IEA					P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0002907	PMID:9915944	PCS		1/4			P	HPO:probinson[2023-03-13]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0000407	PMID:9915944	PCS		1/4			P	HPO:probinson[2023-03-13]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0001757	OMIM:308940	IEA					P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0001417	PMID:9915944	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-13]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0006524	OMIM:308940	IEA					P	HPO:iea[2009-02-17]
OMIM:308940	Leiomyomatosis, diffuse, with alport syndrome		HP:0004722	OMIM:308940	TAS	HP:0003584				P	HPO:skoehler[2012-11-21]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0000473	PMID:25799108	PCS		3/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-05-14]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0003621	PMID:25799108	PCS		4/4			C	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0002015	PMID:25799108	PCS		2/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-05-14]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0001260	PMID:25799108	PCS		3/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-05-14]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0000007	PMID:25799108	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0001304	PMID:25799108	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0001337	OMIM:224500	TAS					P	HPO:skoehler[2015-06-22]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0003677	PMID:25799108	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-14]
OMIM:224500	Dystonia 2, torsion, autosomal recessive		HP:0000643	PMID:25799108	PCS		2/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-05-14]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0000252	PMID:28052917	PCS		2/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0000175	PMID:28052917	PCS		1/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0002540	PMID:28052917	PCS					P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0000750	PMID:28052917	PCS		4/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0003487	PMID:28052917	PCS		4/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0001260	PMID:28052917	PCS		2/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0000193	PMID:28052917	PCS		2/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0030891	PMID:28052917	PCS		4/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0002061	PMID:28052917	PCS		4/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0001270	PMID:28052917	PCS		4/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0012841	PMID:28052917	PCS		2/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0011448	PMID:28052917	PCS		3/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0000407	PMID:28052917	PCS		1/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0100704	PMID:28052917	PCS		1/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0033044	PMID:28052917	PCS		2/4			P	HPO:probinson[2020-08-13]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0000007	PMID:28052917	PCS					I	HPO:probinson[2020-05-07];HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0007663	PMID:28052917	PCS		2/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0000648	PMID:28052917	PCS		1/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0006986	PMID:28052917	PCS		1/4			P	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0003623	PMID:28052917	PCS					C	HPO:probinson[2020-05-07]
OMIM:618768	Spastic paraplegia 81, autosomal recessive		HP:0001347	PMID:28052917	PCS		4/4			P	HPO:probinson[2020-05-07]
OMIM:619476	Joubert syndrome 38		HP:0001320	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000286	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000486	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0004322	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000540	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0030353	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0001263	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0001252	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0011755	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0012506	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0011220	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0007068	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000657	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000007	PMID:28220259	PCS					I	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0002419	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000824	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0002714	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000565	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0002007	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000358	PMID:28220259	PCS		2/2			P	HP:probinson[2021-10-16]
OMIM:619476	Joubert syndrome 38		HP:0000369	PMID:28220259	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:614152	Deafness, autosomal dominant 64		HP:0003676	PMID:21722859	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:614152	Deafness, autosomal dominant 64		HP:0003621	PMID:21722859	PCS					C	HPO:probinson[2023-02-21]
OMIM:614152	Deafness, autosomal dominant 64		HP:0000407	PMID:21722859	PCS		16/16			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-21]
OMIM:614152	Deafness, autosomal dominant 64		HP:0011462	PMID:21722859	PCS					C	HPO:probinson[2023-02-21]
OMIM:614152	Deafness, autosomal dominant 64		HP:0000360	PMID:21722859	PCS		12/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:614152	Deafness, autosomal dominant 64		HP:0000006	PMID:21722859	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:113300	Brachydactyly, type E		HP:0008848	OMIM:113300	IEA					P	HPO:iea[2009-02-17]
OMIM:113300	Brachydactyly, type E		HP:0005863	OMIM:113300	TAS					P	HPO:probinson[2009-02-17]
OMIM:113300	Brachydactyly, type E		HP:0001156	OMIM:113300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:113300	Brachydactyly, type E		HP:0001571	OMIM:113300	IEA					P	HPO:iea[2009-02-17]
OMIM:113300	Brachydactyly, type E		HP:0010049	OMIM:113300	IEA					P	HPO:iea[2009-02-17]
OMIM:113300	Brachydactyly, type E		HP:0006587	OMIM:113300	TAS					P	HPO:probinson[2012-05-27]
OMIM:113300	Brachydactyly, type E		HP:0000311	OMIM:113300	IEA					P	HPO:iea[2009-02-17]
OMIM:113300	Brachydactyly, type E		HP:0000894	OMIM:113300	TAS					P	HPO:probinson[2012-05-27]
OMIM:113300	Brachydactyly, type E		HP:0000006	OMIM:113300	IEA					I	HPO:iea[2009-02-17]
OMIM:113300	Brachydactyly, type E		HP:0010743	OMIM:113300	IEA					P	HPO:iea[2009-02-17]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0025671	OMIM:619462	TAS					P	HPO:probinson[2022-10-05]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0001561	OMIM:619462	TAS	HP:0030674				P	HPO:probinson[2022-10-05]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0001343	OMIM:619462	TAS					P	HPO:probinson[2022-10-05]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0025676	OMIM:619462	TAS					P	HPO:probinson[2022-10-05]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0001791	OMIM:619462	TAS					P	HPO:probinson[2022-10-05]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0002240	OMIM:619462	TAS					P	HPO:probinson[2022-10-05]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0001789	OMIM:619462	TAS					P	HPO:probinson[2022-10-05]
OMIM:619462	Hemolytic disease of fetus and newborn, RH-induced		HP:0001744	OMIM:619462	TAS					P	HPO:probinson[2022-10-05]
OMIM:108720	Atelosteogenesis, type I		HP:0002982	OMIM:108720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:108720	Atelosteogenesis, type I		HP:0005257	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0003196	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0030330	OMIM:108720	TAS					P	HPO:probinson[2015-04-19]
OMIM:108720	Atelosteogenesis, type I		HP:0010049	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:6000952	PMID:23401428	PCS					P	HPO:probinson[2024-08-04]
OMIM:108720	Atelosteogenesis, type I		HP:0009381	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0003826	OMIM:108720	IEA					C	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0000316	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0001602	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0000878	OMIM:108720	TAS					P	HPO:probinson[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0003745	OMIM:108720	IEA					I	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0008417	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0000890	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0000175	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0002990	PMID:24624349	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0003042	PMID:24624349	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:6001057	PMID:24624349	PCS					P	HPO:probinson[2024-08-04]
OMIM:108720	Atelosteogenesis, type I		HP:0011800	OMIM:108720	TAS					P	HPO:skoehler[2013-11-28]
OMIM:108720	Atelosteogenesis, type I		HP:0002949	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0001217	OMIM:108720	TAS					P	HPO:skoehler[2013-01-22]
OMIM:108720	Atelosteogenesis, type I		HP:0001538	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0002986	OMIM:108720	IEA					P	HPO:skoehler[2010-06-20]
OMIM:108720	Atelosteogenesis, type I		HP:0000520	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0000369	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0000006	PMID:14991055	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0003577	PMID:24624349	PCS		1/1			C	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0006406	OMIM:108720	TAS					P	HPO:probinson[2012-06-10]
OMIM:108720	Atelosteogenesis, type I		HP:0008905	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0006408	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0001156	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0001591	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0003097	OMIM:108720	TAS					P	HPO:probinson[2012-06-10]
OMIM:108720	Atelosteogenesis, type I		HP:0005792	OMIM:108720	TAS					P	HPO:probinson[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0002084	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0010743	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0006495	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0008873	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0000774	OMIM:108720	TAS					P	HPO:probinson[2015-02-01]
OMIM:108720	Atelosteogenesis, type I		HP:0004976	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0001622	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0001561	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0009826	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0001762	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0001883	PMID:24624349	PCS		1/1			P	HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0000470	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0000272	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0004592	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0005280	PMID:24624349	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0003417	PMID:24624349	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0003811	OMIM:108720	TAS					C	HPO:skoehler[2013-01-22]
OMIM:108720	Atelosteogenesis, type I		HP:0002007	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:108720	Atelosteogenesis, type I		HP:0000347	PMID:24624349	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-04]
OMIM:108720	Atelosteogenesis, type I		HP:0000028	OMIM:108720	IEA					P	HPO:iea[2009-02-17]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0001265	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0002059	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000252	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0002188	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000343	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000486	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0001321	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000463	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0002079	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0001252	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000592	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0001263	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0005280	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0012110	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000506	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000319	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0012471	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000007	PMID:33463720	PCS					I	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000348	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0000278	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:619304	Pontocerebellar hypoplasia, type 1F		HP:0001510	PMID:33463720	PCS		1/1			P	HPO:probinson[2021-07-06]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0003577	PMID:25192045	PCS		5/5			C	HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0001696	PMID:25192045	PCS		3/5			P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0001651	PMID:25192045	PCS		2/5			P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0002099	OMIM:616037	TAS					P	HPO:skoehler[2014-10-10]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0002110	PMID:25192045	PCS		2/3			P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0033036	PMID:25192045	PCS		1/1			P	HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0012735	PMID:25192045	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0100582	PMID:25192045	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0002093	PMID:25192045	PCS	HP:0003623	4/5			P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0011109	PMID:25192045	PCS		3/5			P	HPO:probinson[2022-12-11];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0200073	PMID:25192045	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0012265	PMID:25192045	PCS		5/5			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0012256	OMIM:616037	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0001629	PMID:25192045	PCS		1/5			P	HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0000007	PMID:25192045	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0000403	PMID:25192045	PCS		2/5			P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0001742	PMID:25192045	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0002205	PMID:25192045	PCS		4/5			P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:616037	Ciliary dyskinesia, primary, 30		HP:0004469	PMID:25192045	PCS		1/5			P	HPO:skoehler[2014-10-10];HPO:probinson[2022-12-11]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000581	OMIM:193500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0003250	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000319	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000635	PMID:33747040;PMID:34456975	PCS		7/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000316	OMIM:193500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0007443	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000912	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0002216	PMID:33747040	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0002414	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0001100	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000574	OMIM:193500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000431	PMID:33747040;PMID:34456975	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0002475	OMIM:193500	TAS		HP:0040283			P	HPO:skoehler[2014-04-04]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000430	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0002211	PMID:33747040;PMID:34456975	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000506	PMID:34456975	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0007990	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0002946	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0007894	OMIM:193500	TAS					P	HPO:probinson[2015-07-19]
OMIM:193500	Waardenburg syndrome, type 1		HP:0005815	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000202	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000664	PMID:33747040;PMID:34456975	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0002227	OMIM:193500	PCS					P	HPO:iea[2012-03-01]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000006	PMID:1347148	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0008527	PMID:34456975	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:193500	Waardenburg syndrome, type 1		HP:0000303	OMIM:193500	IEA					P	HPO:iea[2009-02-17]
OMIM:193500	Waardenburg syndrome, type 1		HP:0002226	OMIM:193500	PCS					P	HPO:iea[2009-02-17]
OMIM:236110	Holzgreve syndrome		HP:0000175	OMIM:236110	IEA					P	HPO:iea[2009-02-17]
OMIM:236110	Holzgreve syndrome		HP:0000089	OMIM:236110	IEA					P	HPO:iea[2009-02-17]
OMIM:236110	Holzgreve syndrome		HP:0001161	OMIM:236110	IEA					P	HPO:iea[2009-02-17]
OMIM:236110	Holzgreve syndrome		HP:0004383	OMIM:236110	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236110	Holzgreve syndrome		HP:0000007	OMIM:236110	IEA					I	HPO:iea[2009-02-17]
OMIM:236110	Holzgreve syndrome		HP:0000204	OMIM:236110	TAS					P	HPO:skoehler[2009-02-17]
OMIM:236110	Holzgreve syndrome		HP:0000104	OMIM:236110	IEA					P	HPO:iea[2009-02-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000164	OMIM:614813	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001792	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000343	PMID:22840364	PCS		5/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001773	PMID:22840364	PCS		5/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0008905	PMID:22840364	PCS		5/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001156	OMIM:614813	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0002164	OMIM:614813	IEA					P	HPO:skoehler[2015-12-30]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001252	PMID:22840364	PCS		1/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001290	OMIM:614813	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0010049	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000060	OMIM:614813	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0008070	OMIM:614813	TAS	HP:0003581				P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0010743	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000819	OMIM:614813	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0100864	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001508	PMID:22840364	PCS		2/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0011220	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000938	PMID:22840364	PCS		1/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0008551	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0009882	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000316	PMID:22840364	PCS		5/5			P	HPO:skoehler[2012-11-16];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0002515	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0030084	OMIM:614813	TAS					P	HPO:skoehler[2014-09-21]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0009765	PMID:22840364	PCS		1/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000455	PMID:22840364	PCS		5/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001620	OMIM:614813	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000256	OMIM:614813	TAS	HP:0011463				P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000798	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000358	PMID:22840364	PCS		5/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000252	OMIM:614813	TAS	HP:0003581				P	HPO:skoehler[2012-11-16];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0008839	OMIM:614813	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0002376	OMIM:614813	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000276	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0003187	OMIM:614813	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000490	OMIM:614813	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001263	PMID:22840364	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0004590	OMIM:614813	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0010579	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001518	PMID:22840364	PCS	HP:0003577	5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000448	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000007	PMID:22840364	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000348	PMID:22840364	PCS		5/5			P	HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000307	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0200055	PMID:22840364	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0001510	OMIM:614813	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000303	OMIM:614813	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000325	PMID:22840364	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-20]
OMIM:614813	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis		HP:0000369	PMID:22840364	PCS		5/5			P	HPO:probinson[2021-10-20]
OMIM:301025	Paganini-Miozzo syndrome		HP:0002003	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0002465	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000341	PMID:30471091	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000020	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0032653	PMID:30471091	PCS		1/2			P	HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0011463	PMID:30471091	PCS		2/2			C	HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0008551	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0002714	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000358	PMID:30471091	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0003348	PMID:30471091	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000494	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0006956	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000750	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000233	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0031936	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0002373	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0011968	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000490	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0001263	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0002151	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000272	PMID:30471091	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0011003	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0001419	PMID:30471091	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000369	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000303	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07]
OMIM:301025	Paganini-Miozzo syndrome		HP:0000325	PMID:30471091	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:619489	Short stature, Dauber-Argente type		HP:0001166	PMID:34272725	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0000252	PMID:26902202;PMID:34272725	PCS		7/7			P	HPO:probinson[2021-10-04];HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0003621	PMID:34272725	PCS		2/2			C	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0000684	PMID:26902202;PMID:34272725	PCS		4/7			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0000331	PMID:26902202;PMID:34272725	PCS		7/7			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0004322	PMID:34272725	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0010511	PMID:26902202	PCS		2/5			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0031107	PMID:26902202	PCS		4/5			P	HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0034184	PMID:34272725	PCS		2/2			P	HPO:probinson[2022-04-15]
OMIM:619489	Short stature, Dauber-Argente type		HP:0008283	PMID:26902202	PCS		3/5			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0000938	PMID:34272725	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0001328	PMID:34272725	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0000007	PMID:26902202	PCS					I	HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0100807	PMID:26902202	PCS		5/5			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0008897	PMID:26902202;PMID:34272725	PCS		7/7			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0004349	PMID:26902202;PMID:34272725	PCS		4/4			P	HPO:probinson[2021-10-04]
OMIM:619489	Short stature, Dauber-Argente type		HP:0000325	PMID:34272725	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002136	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0000252	PMID:27863452	PCS		0/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0003324	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002078	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0031936	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0001321	PMID:27863452	PCS		5/5			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002373	PMID:27863452	PCS		3/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002384	PMID:27863452	PCS		1/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002066	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0001260	PMID:27863452	PCS		5/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002198	PMID:27863452	PCS		5/5			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0001252	PMID:27863452	PCS		5/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0003593	PMID:27863452	PCS		6/6			C	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0011675	PMID:27863452	PCS		0/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0003391	PMID:27863452	PCS		0/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002280	PMID:27863452	PCS		5/5			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002080	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0000007	PMID:27863452	PCS					I	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0007663	PMID:27863452	PCS		0/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002359	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0002599	PMID:27863452	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:620208	Spinocerebellar ataxia, autosomal recessive 33		HP:0009879	PMID:27863452	PCS		0/5			P	HPO:probinson[2023-04-09]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0002421	PMID:32004447	PCS	HP:0003593	4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000463	PMID:32004447	PCS		2/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0010808	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0001252	PMID:32004447	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0002282	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0001270	PMID:32004447	PCS		4/4		HP:0012828	P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0012469	PMID:32004447	PCS		3/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000958	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000518	PMID:32004447	PCS	HP:0011463	1/4		HP:0012832	P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0100704	PMID:32004447	PCS		2/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0002779	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000212	PMID:32004447	PCS		2/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0001601	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0001622	PMID:32004447	IEA		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000154	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0005469	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0002059	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000076	PMID:32004447	PCS		2/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0001344	PMID:32004447	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000574	PMID:32004447	PCS		2/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0002079	PMID:32004447	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000490	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000294	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0011344	PMID:32004447	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0005280	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0011228	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0011471	PMID:32004447	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0009890	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000007	PMID:32004447	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0004429	PMID:32004447	PCS		4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0001257	PMID:32004447	PCS		2/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0002643	PMID:32004447	PCS	HP:0003623	4/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000369	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:618797	Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation		HP:0000248	PMID:32004447	PCS		1/4			P	HPO:probinson[2020-07-19]
OMIM:258150	Spermatogenic failure 1		HP:0030974	PMID:31866047	PCS		2/4			P	HPO:probinson[2021-07-05]
OMIM:258150	Spermatogenic failure 1		HP:0003251	PMID:31866047	PCS	HP:0011462	4/4			P	HPO:probinson[2021-07-05]
OMIM:258150	Spermatogenic failure 1		HP:0011462	PMID:31866047	PCS		4/4			C	HPO:probinson[2022-06-15]
OMIM:258150	Spermatogenic failure 1		HP:0000798	PMID:31866047	PCS		4/4			P	HPO:probinson[2021-07-05]
OMIM:258150	Spermatogenic failure 1		HP:0000006	PMID:31866047	PCS					I	HPO:probinson[2024-01-04]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002069	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000365	PMID:39753114	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000486	PMID:39753114	PCS		2/7			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0031903	PMID:39753114	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002384	PMID:39753114	PCS		4/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001250	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002066	PMID:39753114	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0006829	PMID:39753114	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001252	PMID:39753114	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002061	PMID:39753114	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0032794	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0003390	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0011410	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0045074	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0033725	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000639	PMID:39753114	PCS		0/7			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001643	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0032209	PMID:39753114	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000252	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001382	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001260	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001263	PMID:39753114	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0040196	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000609	PMID:39753114	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0034392	PMID:39753114	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0011451	PMID:39753114	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000767	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000568	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000007	PMID:39753114	PCS					I	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0004209	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000400	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001257	PMID:39753114	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000641	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002104	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0003577	PMID:39753114	PCS		9/9			C	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002164	PMID:39753114	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001272	PMID:39753114	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0007817	PMID:39753114	PCS		2/7			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001270	PMID:39753114	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002080	PMID:39753114	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0008070	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0100543	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0031097	PMID:39753114	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0010550	PMID:39753114	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0033078	PMID:39753114	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000657	PMID:39753114	PCS		2/8			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0007663	PMID:39753114	PCS		0/7			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0009004	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000219	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001945	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000218	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001623	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001347	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0003128	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0008936	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002059	PMID:39753114	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002015	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000750	PMID:39753114	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002133	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001762	PMID:39753114	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000276	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001684	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002376	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001321	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002131	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0005484	PMID:39753114	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002808	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0009830	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001317	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001999	PMID:39753114	PCS		2/8			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002804	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000505	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001511	PMID:39753114	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0001159	PMID:39753114	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0002445	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0003259	PMID:39753114	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000666	PMID:39753114	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:621102	Neurodevelopmental disorder with progressive spasticity and brain abnormalities		HP:0000347	PMID:39753114	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-10-02]
OMIM:166760	Otitis media, susceptibility to		HP:0000403	PMID:26121085	PCS					P	HPO:iea[2009-02-17];HP:probinson[2018-09-16]
OMIM:166760	Otitis media, susceptibility to		HP:0010982	PMID:26121085	PCS					I	HP:probinson[2018-09-16]
OMIM:166760	Otitis media, susceptibility to		HP:0000006	OMIM:166760	IEA					I	HPO:skoehler[2019-04-18]
OMIM:215050	Chondrodysplasia calcificans metaphysealis		HP:0003510	OMIM:215050	TAS					P	HPO:probinson[2009-02-17]
OMIM:215050	Chondrodysplasia calcificans metaphysealis		HP:0005871	OMIM:215050	TAS					P	HPO:probinson[2009-02-17]
OMIM:215050	Chondrodysplasia calcificans metaphysealis		HP:0008155	OMIM:215050	TAS					P	HPO:probinson[2009-02-17]
OMIM:215050	Chondrodysplasia calcificans metaphysealis		HP:0000007	OMIM:215050	TAS					I	HPO:probinson[2009-02-17]
OMIM:215050	Chondrodysplasia calcificans metaphysealis		HP:0100255	OMIM:215050	TAS					P	HPO:probinson[2009-02-17]
OMIM:301031	Congenital disorder of glycosylation, type Icc		HP:0003642	PMID:31036665	PCS		2/2			P	HPO:probinson[2020-07-24]
OMIM:301031	Congenital disorder of glycosylation, type Icc		HP:0001419	PMID:31036665	PCS					I	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301031	Congenital disorder of glycosylation, type Icc		HP:0001263	PMID:31036665	PCS		2/2			P	HPO:probinson[2020-07-24]
OMIM:301031	Congenital disorder of glycosylation, type Icc		HP:0002240	PMID:31036665	PCS		1/2			P	HPO:probinson[2020-07-24]
OMIM:301031	Congenital disorder of glycosylation, type Icc		HP:0001249	PMID:31036665	IEA		2/2			P	HPO:probinson[2020-07-24]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001397	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002089	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0003530	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000260	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001252	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002240	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0003076	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0003150	OMIM:231680	TAS					P	HPO:probinson[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000519	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001943	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0025734	PMID:32550677	PCS					P	HPO:probinson[2024-06-29]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002614	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000114	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001302	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001324	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002018	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000113	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000256	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000377	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0003647	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000952	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001325	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001941	OMIM:231680	IEA					P	HPO:skoehler[2019-09-07]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000078	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002013	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002098	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002171	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0005280	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0002909	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000506	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000803	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0001999	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000007	OMIM:231680	IEA					I	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0000348	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0003219	OMIM:231680	IEA					P	HPO:iea[2009-02-17]
OMIM:231680	Multiple acyl-CoA-dehydrogenase deficiency		HP:0003811	OMIM:231680	IEA					C	HPO:iea[2009-02-17]
OMIM:266900	Senior-Loken syndrome 1		HP:0003774	PMID:9856524	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0003621	PMID:9856524	PCS		7/8			C	HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0005576	PMID:9856524	PCS		1/1			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0000083	PMID:9856524	PCS		1/8			P	HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0020132	PMID:9856524	PCS		1/1			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0000090	OMIM:266900	TAS	HP:0003621				P	HPO:probinson[2014-01-18]
OMIM:266900	Senior-Loken syndrome 1		HP:0001959	PMID:9856524	PCS		4/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0001903	OMIM:266900	IEA					P	HPO:iea[2009-02-17]
OMIM:266900	Senior-Loken syndrome 1		HP:0011462	PMID:9856524	PCS		1/8			C	HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0000007	PMID:9856524	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0004727	PMID:9856524	PCS		3/8			P	HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0000103	PMID:9856524	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0003259	PMID:9856524	PCS		2/8			P	HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0001249	PMID:9856524	PCS		1/8			P	HPO:probinson[2022-09-03]
OMIM:266900	Senior-Loken syndrome 1		HP:0000556	PMID:9856524	PCS		5/6			P	HPO:probinson[2022-09-03]
OMIM:162260	Neurofibromatosis, type III, mixed central and peripheral		HP:0007429	OMIM:162260	IEA					P	HPO:iea[2009-02-17]
OMIM:162260	Neurofibromatosis, type III, mixed central and peripheral		HP:0002858	OMIM:162260	IEA					P	HPO:iea[2009-02-17]
OMIM:162260	Neurofibromatosis, type III, mixed central and peripheral		HP:0006751	OMIM:162260	IEA					P	HPO:iea[2009-02-17]
OMIM:162260	Neurofibromatosis, type III, mixed central and peripheral		HP:0007576	OMIM:162260	IEA					P	HPO:iea[2009-02-17]
OMIM:162260	Neurofibromatosis, type III, mixed central and peripheral		HP:0009589	OMIM:162260	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162260	Neurofibromatosis, type III, mixed central and peripheral		HP:0000006	OMIM:162260	IEA					I	HPO:iea[2009-02-17]
OMIM:162260	Neurofibromatosis, type III, mixed central and peripheral		HP:0009737	OMIM:162260	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614807	Myopathy, centronuclear, 4		HP:0003687	PMID:22818856	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0001250	PMID:22818856	PCS		1/5			P	HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0001252	PMID:22818856	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0001270	PMID:22818856	PCS		2/5			P	HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0040081	PMID:22818856	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0011463	PMID:22818856	PCS		3/5			C	HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0003803	PMID:22818856	PCS		2/3			P	HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0001324	PMID:22818856	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0002359	PMID:22818856	PCS		3/5			P	HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0000006	PMID:22818856	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0001249	PMID:22818856	PCS		1/5			P	HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0003326	PMID:22818856	PCS		3/5			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0003546	PMID:22818856	PCS		4/5			P	HPO:probinson[2022-11-08]
OMIM:614807	Myopathy, centronuclear, 4		HP:0003623	PMID:22818856	PCS		2/5			C	HPO:probinson[2022-11-08]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003400	OMIM:214400	IEA					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0001265	OMIM:214400	IEA					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0002751	OMIM:214400	IEA		HP:0040282			P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003431	PMID:11743579	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0001178	OMIM:214400	IEA					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003693	OMIM:214400	TAS					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0006915	OMIM:214400	IEA					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003383	PMID:11743579	PCS		2/2			P	HPO:probinson[2022-09-03]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0001284	OMIM:214400	IEA					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0002460	OMIM:214400	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2013-02-23]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003593	PMID:11743579	PCS					C	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003382	OMIM:214400	IEA					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0001270	OMIM:214400	IEA					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003380	PMID:11743579	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0040078	OMIM:214400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0000007	PMID:11743579	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0002936	OMIM:214400	TAS					P	HPO:skoehler[2013-02-25]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003429	OMIM:214400	TAS					P	HPO:skoehler[2014-05-04]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003448	PMID:11743579	PCS		8/8			P	HPO:probinson[2022-09-03]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0007107	PMID:11743579	PCS		2/2			P	HPO:probinson[2022-09-03]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0001765	OMIM:214400	TAS					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0000764	OMIM:214400	PCS					P	HPO:probinson[2009-02-17]
OMIM:214400	Charcot-Marie-Tooth disease, type 4A		HP:0003678	OMIM:214400	TAS					C	HPO:probinson[2009-02-17]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0000939	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0000938	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0000117	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0002150	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0003109	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0002659	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0000006	OMIM:612286	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0000787	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612286	Nephrolithiasis/osteoporosis, hypophosphatemic, 1		HP:0002148	OMIM:612286	IEA					P	HPO:skoehler[2010-06-19]
OMIM:259500	Osteosarcoma		HP:0001442	OMIM:259500	TAS					I	HPO:skoehler[2019-09-07]
OMIM:259500	Osteosarcoma		HP:0009919	OMIM:259500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:259500	Osteosarcoma		HP:0002669	OMIM:259500	IEA					P	HPO:iea[2009-02-17]
OMIM:210100	Beta-aminoisobutyric acid, urinary excretion of		HP:0032480	PMID:21572414	PCS					P	HPO:probinson[2020-09-06]
OMIM:210100	Beta-aminoisobutyric acid, urinary excretion of		HP:0000007	PMID:21572414	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-06]
OMIM:613826	Leber congenital amaurosis 6		HP:0001133	PMID:29193763;PMID:17306875;PMID:31666973	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000563	PMID:24066033;PMID:26047050;PMID:31666973	PCS		1/15			P	HPO:probinson[2013-08-10];HPO:probinson[2024-11-02];ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000486	PMID:18682808;PMID:30576320	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0030211	PMID:33308271	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0003593	PMID:29053603;PMID:30072743;PMID:23505306;PMID:25096270;PMID:21602930;PMID:33308271;PMID:27422788;PMID:26047050;PMID:23661368;PMID:30576320;PMID:31666973	PCS		42/53			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000518	PMID:28453600;PMID:30576320;PMID:31666973	PCS		1/9			P	HPO:probinson[2013-08-10];HPO:probinson[2024-11-02];ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000639	PMID:23505306;PMID:30072743;PMID:25096270;PMID:24997176;PMID:33308271;PMID:27422788;PMID:32736544;PMID:28966547;PMID:30576320;PMID:24066033;PMID:29053603;PMID:28456785;PMID:21602930;PMID:26047050;PMID:31666973	PCS		64/66			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0011463	PMID:26992781;PMID:30072743;PMID:29193763;PMID:17306875;PMID:26047050	PCS		10/21			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0032122	PMID:28456785;PMID:24997176;PMID:33308271;PMID:27422788;PMID:26047050;PMID:34722527;PMID:23661368;PMID:30576320	PCS		35/39			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0008499	OMIM:613826	TAS					P	HPO:probinson[2013-08-10]
OMIM:613826	Leber congenital amaurosis 6		HP:0007720	PMID:24066033	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0007401	PMID:29193763;PMID:30072743;PMID:27422788;PMID:18682808;PMID:26047050;PMID:31666973	PCS		6/28			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0007843	PMID:23505306;PMID:17306875;PMID:21602930;PMID:27422788;OMIM:613826;PMID:23661368;PMID:28966547;PMID:31666973	PCS		33/38			P	ORCID:0000-0002-0736-9199[2024-11-02];HPO:probinson[2013-08-10]
OMIM:613826	Leber congenital amaurosis 6		HP:0000512	PMID:29053603;PMID:26992781;PMID:23505306;PMID:28456785;PMID:21602930;PMID:33308271;PMID:27422788;PMID:34722527;PMID:28453600;PMID:32736544;PMID:28966547;PMID:31666973	PCS		34/34			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0001249	PMID:28456785	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0003623	PMID:33308271;PMID:34722527	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0025010	PMID:29193763	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0001263	PMID:23505306;PMID:28456785;PMID:24997176;PMID:33308271;PMID:32736544;PMID:28453600	PCS		6/30			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0001141	PMID:29053603	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0030825	PMID:26992781;PMID:21602930	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0200070	PMID:30072743;PMID:18682808	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0008043	PMID:28456785	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000007	OMIM:613826	TAS					I	HPO:probinson[2013-01-09]
OMIM:613826	Leber congenital amaurosis 6		HP:0000648	PMID:30072743;PMID:18682808;PMID:28966547	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0004327	PMID:26047050	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0007737	PMID:23505306;PMID:17306875;PMID:26047050;PMID:32736544;PMID:28453600	PCS		7/22			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0003577	PMID:28456785;PMID:24997176;PMID:32736544;PMID:28453600;PMID:30576320	PCS		20/21			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0007814	PMID:24066033;PMID:29053603;PMID:29193763;PMID:23505306;PMID:24997176;PMID:33308271;PMID:27422788;PMID:26047050;PMID:28453600;PMID:32736544;PMID:30576320	PCS		33/46			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000662	PMID:29193763;PMID:17306875;PMID:25096270;PMID:31666973	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000540	PMID:24066033;PMID:23505306;PMID:24997176;PMID:33308271;PMID:27422788;PMID:26047050;PMID:28966547	PCS		36/39			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0030553	PMID:21602930	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0030672	PMID:30072743;PMID:18682808	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0030515	PMID:29193763;PMID:17306875	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000613	PMID:26992781;PMID:23505306;PMID:21602930;PMID:33308271;PMID:18682808;PMID:32736544	PCS		8/23			P	HPO:probinson[2013-08-10];HPO:probinson[2024-11-02];ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0007663	PMID:26992781;PMID:23505306;PMID:30072743;PMID:25096270;PMID:21602930;PMID:18682808;PMID:26047050;PMID:28453600;PMID:32736544;PMID:30576320;PMID:31666973	PCS		38/38			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0007787	PMID:29193763;PMID:30072743;PMID:18682808	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000533	PMID:18682808;PMID:31666973	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000577	PMID:26047050	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000550	OMIM:613826	TAS					P	HPO:probinson[2013-08-10]
OMIM:613826	Leber congenital amaurosis 6		HP:0003621	PMID:28966547;PMID:31666973	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000551	PMID:30072743	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0001483	PMID:24066033;PMID:23505306;PMID:24997176;PMID:21602930;PMID:33308271;PMID:27422788;PMID:26047050;PMID:32736544;PMID:23661368;PMID:28966547;PMID:31666973	PCS		35/57			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0011504	PMID:30072743;PMID:18682808	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0030329	PMID:25096270;PMID:33308271	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0012045	PMID:29193763	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0012043	OMIM:613826	TAS					P	HPO:probinson[2013-08-10]
OMIM:613826	Leber congenital amaurosis 6		HP:0000546	PMID:26992781;PMID:21602930;PMID:27422788;PMID:26047050;PMID:23661368	PCS		19/20			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000543	PMID:24066033;PMID:33308271;PMID:18682808;PMID:27422788;PMID:28453600;PMID:28966547	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:613826	Leber congenital amaurosis 6		HP:0000545	PMID:24066033;PMID:29193763;PMID:28966547	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0002421	PMID:27904971	PCS		1/1			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0000252	PMID:27904971;PMID:31754459	PCS		3/3			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0002059	PMID:27904971;PMID:31754459	PCS		3/3			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0002079	PMID:27904971;PMID:31754459	PCS		3/3			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0001250	PMID:31754459	PCS		1/2			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0001272	PMID:31754459	PCS		1/2			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0002572	PMID:31754459	PCS		1/2			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0001263	PMID:27904971	PCS		1/1			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0003593	PMID:31754459	PCS		2/2			C	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0100021	PMID:27904971	PCS		1/1			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0002280	PMID:31754459	PCS		1/2			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0012110	PMID:27904971	PCS		1/1			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0011471	PMID:27904971	PCS		1/1			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0000639	PMID:27904971;PMID:31754459	PCS		3/3			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0100759	PMID:31754459	PCS		1/2			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0009830	PMID:31754459	PCS					P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0000007	PMID:27904971	PCS					I	HPO:probinson[2020-09-11];HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0001257	PMID:31754459	PCS		1/2			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0002126	PMID:27904971	PCS		1/1			P	HPO:probinson[2020-09-11]
OMIM:618973	Neurodegeneration, infantile-onset, biotin-responsive		HP:0004315	PMID:31754459	PCS		2/2			P	HPO:probinson[2020-09-11]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0003376	OMIM:606595	IEA					P	HPO:probinson[2009-02-17]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0003596	PMID:15122254	PCS		4/7			C	HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0003431	PMID:15122254	PCS				HP:0012825	P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0001178	OMIM:606595	IEA					P	HPO:probinson[2009-02-17]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0001761	PMID:15122254	PCS		6/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0003584	PMID:15122254	PCS		1/7			C	HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0003394	PMID:15122254	PCS		1/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0002460	PMID:15122254	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0002380	PMID:15122254	PCS		1/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0034337	PMID:15122254	PCS		3/7			P	HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0009027	PMID:15122254	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0002936	PMID:15122254	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0007267	PMID:15122254	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0025710	PMID:15122254	PCS		2/7			C	HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0012391	PMID:15122254	PCS		4/7			P	HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0009129	PMID:15122254	PCS		7/7			P	HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0000006	PMID:15122254	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0002522	PMID:15122254	PCS		6/7			P	HPO:probinson[2023-03-31]
OMIM:606595	Charcot-Marie-Tooth disease, axonal, type 2F		HP:0008944	PMID:15122254	PCS		7/7			P	HPO:probinson[2023-03-31]
OMIM:166990	Osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia,hydrocephalus, and hypertension		HP:0008905	OMIM:166990	TAS					P	HPO:probinson[2009-02-17]
OMIM:166990	Osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia,hydrocephalus, and hypertension		HP:0001274	OMIM:166990	IEA					P	HPO:iea[2009-02-17]
OMIM:166990	Osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia,hydrocephalus, and hypertension		HP:0000822	OMIM:166990	IEA					P	HPO:iea[2009-02-17]
OMIM:166990	Osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia,hydrocephalus, and hypertension		HP:0000238	OMIM:166990	IEA					P	HPO:iea[2009-02-17]
OMIM:166990	Osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia,hydrocephalus, and hypertension		HP:0001873	OMIM:166990	IEA					P	HPO:iea[2009-02-17]
OMIM:166990	Osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia,hydrocephalus, and hypertension		HP:0000006	OMIM:166990	IEA					I	HPO:iea[2009-02-17]
OMIM:607847	Neutropenia, nonimmune chronic idiopathic, of adults		HP:0004808	OMIM:607847	TAS		HP:0040283			P	HPO:probinson[2013-03-04]
OMIM:607847	Neutropenia, nonimmune chronic idiopathic, of adults		HP:0000006	OMIM:607847	TAS					I	HPO:probinson[2013-01-09]
OMIM:607847	Neutropenia, nonimmune chronic idiopathic, of adults		HP:0001875	OMIM:607847	TAS				HP:0012825	P	HPO:probinson[2013-03-04]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0002059	PMID:24011989	PCS		1/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0000252	PMID:24011989	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0003577	PMID:24011989	PCS		5/7			C	HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0000486	PMID:24011989	PCS		5/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001332	PMID:24011989	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001272	PMID:24011989	PCS		1/3			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001250	PMID:24011989	PCS		3/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001263	PMID:24011989	PCS		7/7			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0006808	PMID:24011989	PCS		3/3			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0003593	PMID:24011989	PCS		2/7			C	HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001508	PMID:24011989	PCS		7/7			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0000407	PMID:24011989	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001419	PMID:24011989	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001999	OMIM:300475	TAS					P	HPO:skoehler[2013-11-18]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0007256	PMID:24011989	PCS		6/6			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0000648	PMID:24011989	PCS		2/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0001511	PMID:24011989	PCS		3/7			P	HPO:probinson[2023-03-26]
OMIM:300475	Deafness, dystonia, and cerebral hypomyelination		HP:0002445	PMID:24011989	PCS		5/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0001650	PMID:21683322	PCS		1/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0000343	PMID:21683322	PCS					P	HPO:skoehler[2013-05-21];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0001773	PMID:21683322	PCS		19/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0001376	PMID:21683322	TAS		19/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0004322	PMID:21683322	PCS		19/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0003196	PMID:21683322	PCS					P	HPO:skoehler[2015-10-05];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0002240	PMID:21683322	PCS		5/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0001072	PMID:21683322	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0010446	PMID:21683322	PCS		3/19			P	HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0000319	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0000316	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0000219	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0004279	PMID:21683322	PCS		19/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0002750	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0001387	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0003300	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0000293	PMID:21683322	PCS					P	HPO:skoehler[2013-05-21];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0002092	PMID:21683322	PCS		1/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0002093	PMID:21683322	PCS		5/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0010579	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0001718	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0030051	PMID:21683322	PCS					P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-26]
OMIM:614185	Geleophysic dysplasia 2		HP:0001653	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0000006	PMID:21683322	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:614185	Geleophysic dysplasia 2		HP:0001634	PMID:21683322	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2019-07-18]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001387	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001382	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0005180	PMID:17190868	PCS		11/14	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0005180	PMID:17190868	PCS		9/30	FEMALE		P	HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0011580	OMIM:314400	PCS					P	HPO:probinson[2012-04-08]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001939	OMIM:314400	IEA					P	HPO:iea[2009-02-17]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0006692	OMIM:314400	PCS					P	HPO:probinson[2012-04-08]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0012471	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0000508	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001647	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0000316	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001635	OMIM:314400	IEA					P	HPO:iea[2009-02-17]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001659	PMID:17190868	PCS		13/14	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001417	PMID:17190868	PCS					I	HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001653	PMID:17190868	PCS		14/14	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001653	PMID:17190868	PCS		23/30	FEMALE		P	HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001634	OMIM:314400	IEA					P	HPO:iea[2009-02-17]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001634	PMID:17190868	PCS		12/14	MALE		P	HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0001634	PMID:17190868	PCS		4/30	FEMALE		P	HPO:probinson[2022-10-11]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0000336	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:314400	Cardiac valvular dysplasia, X-linked		HP:0000973	OMIM:314400	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:602081	Speech-language disorder-1		HP:0006977	PMID:11586359	PCS					P	HPO:probinson[2022-08-27]
OMIM:602081	Speech-language disorder-1		HP:0000750	PMID:11586359	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:602081	Speech-language disorder-1		HP:0002134	PMID:11586359	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:602081	Speech-language disorder-1		HP:0011463	PMID:11586359	PCS					C	HPO:probinson[2022-08-27]
OMIM:602081	Speech-language disorder-1		HP:0007301	PMID:11586359	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-27]
OMIM:602081	Speech-language disorder-1		HP:0002546	PMID:11586359	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:602081	Speech-language disorder-1		HP:0000006	PMID:11586359	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:612292	Birk-Barel syndrome		HP:0002553	PMID:27151206	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000341	PMID:27151206	PCS		4/4			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0002015	PMID:27151206	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0011819	PMID:27151206	PCS		8/19			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0010804	PMID:27151206	PCS		11/19			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000276	PMID:27151206	PCS		8/19			P	HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000193	PMID:27151206	PCS		1/19			P	HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0001263	PMID:27151206	PCS		4/4			P	HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0001252	PMID:27151206	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000308	PMID:27151206	PCS		13/19			P	HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000954	PMID:27151206	PCS		3/19			P	HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0008872	PMID:27151206	PCS	HP:0003593	4/4			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000527	PMID:27151206	PCS		10/19			P	HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0003758	PMID:27151206	PCS		8/19			P	HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000218	PMID:27151206	PCS		8/19			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000960	PMID:27151206	PCS		1/4			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000322	PMID:27151206	PCS		13/19			P	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0000006	PMID:27151206	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2020-07-22]
OMIM:612292	Birk-Barel syndrome		HP:0001249	PMID:27151206	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-22]
OMIM:611943	Riddle syndrome		HP:0000252	OMIM:611943	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:611943	Riddle syndrome		HP:0004322	PMID:17940005	PCS					P	HPO:probinson[2013-01-09]
OMIM:611943	Riddle syndrome		HP:0000958	OMIM:611943	TAS					P	HPO:skoehler[2014-08-24]
OMIM:611943	Riddle syndrome		HP:0011342	PMID:17940005	PCS					P	HPO:probinson[2013-04-03]
OMIM:611943	Riddle syndrome		HP:0011133	PMID:17940005	PCS					P	HPO:probinson[2013-04-03]
OMIM:611943	Riddle syndrome		HP:0001251	OMIM:611943	TAS					P	HPO:skoehler[2014-08-24]
OMIM:611943	Riddle syndrome		HP:0001999	PMID:17940005	PCS					P	HPO:probinson[2013-04-03]
OMIM:611943	Riddle syndrome		HP:0000007	PMID:19203578	PCS					I	HPO:probinson[2013-04-03]
OMIM:611943	Riddle syndrome		HP:0002206	OMIM:611943	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:611943	Riddle syndrome		HP:0002721	PMID:17940005	PCS					P	HPO:probinson[2013-04-03]
OMIM:611943	Riddle syndrome		HP:0004315	PMID:17940005	PCS					P	HPO:probinson[2013-04-03]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0002188	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000343	PMID:37711075	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000486	PMID:37711075	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0001250	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0003593	PMID:37711075	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0032794	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0001270	PMID:37711075	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0012389	PMID:37711075	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0033725	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000639	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0011463	PMID:37711075	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000718	PMID:37711075	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000316	PMID:37711075	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0001249	PMID:37711075	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0006855	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0008936	PMID:37711075	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0003202	PMID:37711075	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000252	PMID:37711075	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000750	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0002353	PMID:37711075	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000233	PMID:37711075	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0001344	PMID:37711075	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000276	PMID:37711075	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0001263	PMID:37711075	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0003160	PMID:37711075	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0034392	PMID:37711075	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0032792	PMID:37711075	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000448	PMID:37711075	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000007	PMID:37711075	PCS					I	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000505	PMID:37711075	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000400	PMID:37711075	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0001257	PMID:37711075	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620546	Congenital disorder of glycosylation, type IIbb		HP:0000369	PMID:37711075	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:127700	Dyslexia, susceptibility to, 1		HP:0002167	OMIM:127700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:127700	Dyslexia, susceptibility to, 1		HP:0010522	OMIM:127700	TAS					P	HPO:skoehler[2010-06-18]
OMIM:127700	Dyslexia, susceptibility to, 1		HP:0000006	OMIM:127700	TAS					I	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0008209	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001894	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001371	OMIM:212065	TAS					P	HPO:probinson[2012-04-11]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001250	PMID:11134235	PCS		5/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001252	PMID:11343337;PMID:11134235	PCS		19/23			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07];HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001251	PMID:11343337;OMIM:212065	PCS		12/13			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003593	PMID:11343337;PMID:11134235	PCS		19/23			C	HPO:probinson[2022-05-07];HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003073	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001929	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000639	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0011463	PMID:11343337	PCS		1/3			C	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0011220	OMIM:212065	TAS					P	HPO:probinson[2012-04-11]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0020045	PMID:11343337	PCS		2/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001522	PMID:11134235	PCS		4/20			C	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001324	OMIM:212065	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2012-04-11]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000114	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000510	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0004315	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003623	PMID:11134235	PCS		2/20			C	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001265	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003642	PMID:11343337;PMID:11134235	PCS		23/23			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07];HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000252	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002197	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002198	PMID:11343337	PCS		2/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001260	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001263	PMID:11343337;PMID:11134235	PCS		21/23			P	HPO:probinson[2022-05-18];HPO:probinson[2012-04-11];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000093	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000969	PMID:11134235	PCS		2/20			P	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0007552	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000007	OMIM:212065	IEA					I	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001976	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0007874	PMID:11343337	PCS		3/3			P	HPO:probinson[2022-05-18];HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000565	OMIM:212065	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000400	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001698	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001337	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001397	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003577	PMID:11343337	PCS		1/3			C	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001310	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000100	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001272	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001271	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001395	PMID:11134235	PCS		4/4			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002240	PMID:11134235	PCS		12/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001790	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002280	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002080	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0008151	OMIM:212065	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001508	OMIM:212065	IEA		13/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000815	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000938	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0008872	OMIM:212065	TAS					P	HPO:probinson[2012-04-11]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001701	PMID:11134235	PCS		5/20			P	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000219	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002910	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001347	PMID:11343337	PCS		1/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003645	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001320	PMID:11343337	PCS		2/3			P	HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002014	PMID:11134235	PCS		5/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0006955	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:6000781	PMID:11343337	PCS		3/3			P	HPO:probinson[2024-06-29]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000750	PMID:11343337	PCS		2/3			P	HPO:probinson[2022-05-18];HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001321	PMID:11134235	PCS		18/20			P	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003146	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002013	PMID:11134235	PCS		4/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001560	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001284	PMID:11134235	PCS		11/20			P	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003186	PMID:11343337	PCS		0/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-18]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002570	PMID:11134235	PCS		1/18			P	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0005280	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0003819	PMID:11134235	PCS		1/20			C	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002808	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0011473	PMID:11134235	PCS		2/4			P	HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000107	PMID:11134235	PCS		11/16			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0000821	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0001638	PMID:11134235	PCS		2/20			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002720	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:212065	Congenital disorder of glycosylation, type Ia		HP:0002401	OMIM:212065	IEA					P	HPO:skoehler[2009-02-17]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0002751	PMID:17100996	PCS		1/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0002650	PMID:17100996	PCS		4/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0000750	PMID:17100996	PCS		3/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0000232	PMID:17100996	PCS		5/6			P	HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0001252	PMID:17100996	PCS		2/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0001270	PMID:17100996	PCS		1/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0001518	PMID:17100996	PCS		1/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0011220	PMID:17100996	PCS		4/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0001833	PMID:17100996	PCS		1/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0000678	PMID:17100996	PCS		1/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0001417	PMID:17100996	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0001423	PMID:10319851	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0000455	PMID:17100996	PCS		4/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0000179	PMID:17100996	PCS		5/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2021-09-26]
OMIM:300844	Intellectual developmental disorder, X-linked 19		HP:0001249	PMID:17100996	PCS		5/6	MALE		P	HPO:probinson[2013-02-21];HPO:probinson[2021-09-26]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0003236	PMID:9731526	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-09]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0003621	PMID:9731526	PCS					C	HPO:probinson[2023-02-09]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0003198	PMID:9731526	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0011462	PMID:9731526	PCS					C	HPO:probinson[2023-02-09]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0000007	PMID:9731526	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0002505	PMID:9731526	PCS	HP:0003581				P	HPO:probinson[2023-02-09]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0003701	PMID:9731526	PCS					P	HPO:probinson[2023-02-09]
OMIM:606768	Myopathy, distal, with anterior tibial onset		HP:0003678	PMID:9731526	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:619648	Zaki syndrome		HP:0001770	PMID:34587386	PCS		5/7			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0004322	PMID:34587386	PCS		6/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001250	PMID:34587386	PCS		1/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001252	PMID:34587386	PCS		2/8		HP:0012825	P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0003593	PMID:34587386	PCS		8/10			C	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002064	PMID:34587386	PCS		1/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0045075	PMID:34587386	PCS		3/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0034185	PMID:34587386	PCS		3/8			P	HPO:probinson[2022-04-15]
OMIM:619648	Zaki syndrome		HP:0001800	PMID:34587386	PCS		2/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0100807	PMID:34587386	PCS		3/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001643	PMID:34587386	PCS		1/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001249	PMID:34587386	PCS		8/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000252	PMID:34587386	PCS		9/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002079	PMID:34587386	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002198	PMID:34587386	PCS		2/5			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002194	PMID:34587386	PCS		6/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0100257	PMID:34587386	PCS		1/10			P	HPO:probinson[2022-02-20];HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000007	PMID:34587386	PCS					I	HPO:probinson[2022-02-20];HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000960	PMID:34587386	PCS		1/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000322	PMID:34587386	PCS		8/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000126	PMID:34587386	PCS		1/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001655	PMID:34587386	PCS		2/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0005338	PMID:34587386	PCS		3/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000445	PMID:34587386	PCS		8/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001276	PMID:34587386	PCS		1/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0003577	PMID:34587386	PCS		2/10			C	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000384	PMID:34587386	PCS		1/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000340	PMID:34587386	PCS		3/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000463	PMID:34587386	PCS		3/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0010862	PMID:34587386	PCS		3/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0010746	PMID:34587386	PCS		2/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0012488	PMID:34587386	PCS		1/5			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002317	PMID:34587386	PCS		1/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000218	PMID:34587386	PCS		8/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000378	PMID:34587386	PCS		8/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0006610	PMID:34587386	PCS		4/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000776	PMID:34587386	PCS		1/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000974	PMID:34587386	PCS		2/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001347	PMID:34587386	PCS		1/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0001320	PMID:34587386	PCS		3/5			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000154	PMID:34587386	PCS		8/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000750	PMID:34587386	PCS		2/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002650	PMID:34587386	PCS		2/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000431	PMID:34587386	PCS		6/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002376	PMID:34587386	PCS		1/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0004396	PMID:34587386	PCS		3/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0012434	PMID:34587386	PCS		2/10			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0002209	PMID:34587386	PCS		8/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000348	PMID:34587386	PCS		3/8			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0009836	PMID:34587386	PCS		4/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000347	PMID:34587386	PCS		6/9			P	HPO:probinson[2022-02-20]
OMIM:619648	Zaki syndrome		HP:0000104	PMID:34587386	PCS		1/9			P	HPO:probinson[2022-02-20]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002311	PMID:28777935	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002136	OMIM:617665	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002345	PMID:28777935	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002353	PMID:28777935	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002650	PMID:28777935	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002133	PMID:28777935	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0001250	PMID:28777935	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0001382	PMID:28777935	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002121	PMID:28777935	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0001263	PMID:28777935	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0001252	PMID:28777935	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0001251	PMID:28777935	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0003593	PMID:28777935	PCS		4/4			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0032794	PMID:28777935	PCS		2/4			P	HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0002392	PMID:28777935	PCS		1/2			P	HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0008770	PMID:28777935	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0000739	OMIM:617665	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0011153	PMID:28777935	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0007018	PMID:28777935	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0000006	PMID:28777935	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-15]
OMIM:617665	Epileptic encephalopathy, early infantile, 56		HP:0001249	PMID:28777935	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-15]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0007737	PMID:11868161	PCS		0/26			P	HPO:probinson[2013-03-04];HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0000662	PMID:11868161	PCS	HP:0003593	26/26			P	HPO:probinson[2013-03-04];HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0000551	PMID:11868161	PCS		20/20			P	HPO:probinson[2013-03-04];HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0003593	PMID:11868161	PCS		26/26			C	HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0000007	PMID:11868161	PCS					I	HPO:probinson[2013-01-09]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0007663	PMID:11868161	PCS		26/26			P	HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0030529	PMID:11868161	PCS		8/26			P	HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0000603	PMID:11868161	PCS		6/26			P	HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0000575	PMID:11868161	PCS		23/24			P	HPO:probinson[2013-03-04];HPO:probinson[2024-03-13]
OMIM:607476	Newfoundland rod-cone dystrophy		HP:0000556	PMID:11868161	PCS					P	HPO:probinson[2013-03-04]
OMIM:615072	Brachydactyly, type A1, C		HP:0003038	PMID:20683927	PCS		0/4			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0001156	PMID:20683927	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:lccarmody[2018-10-02];HP:probinson[2019-01-03];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0004322	PMID:20683927	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0009295	PMID:20683927	PCS		4/4			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0010034	PMID:20683927	PCS		4/4			P	HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0004220	PMID:20683927	PCS		4/4			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0009882	PMID:20683927	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:615072	Brachydactyly, type A1, C		HP:0009577	PMID:20683927	PCS		4/4			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0000007	PMID:20683927	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0000006	PMID:20683927	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0001776	PMID:20683927	PCS		2/4			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-15]
OMIM:615072	Brachydactyly, type A1, C		HP:0009439	PMID:20683927	PCS		4/4			P	HPO:lccarmody[2018-10-02];HPO:probinson[2024-03-15]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001254	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003596	PMID:29302025	PCS		1/3			C	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001695	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0005575	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001250	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000083	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001252	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003153	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003593	PMID:16311595;PMID:29302025	PCS		133/175			C	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001290	OMIM:277400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000639	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0011463	PMID:16311595	PCS		11/172			C	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000319	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0011462	PMID:16311595	PCS		4/172			C	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001889	PMID:29302025	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000238	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001649	PMID:29302025	PCS		2/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002615	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001249	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003623	PMID:29302025	PCS		1/3			C	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000252	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001662	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002156	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003286	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001263	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000093	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002071	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000726	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000007	PMID:16311595	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000400	OMIM:277400	TAS					P	HPO:iea[2013-08-07]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000369	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001337	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000980	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002120	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003210	PMID:29302025	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002240	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000580	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002160	PMID:29302025	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001907	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001508	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0008872	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0007663	OMIM:277400	TAS					P	HPO:skoehler[2015-07-26]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002912	PMID:29302025;OMIM:277400	PCS		12/13			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001942	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003524	PMID:29302025	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0008936	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003621	PMID:16311595	PCS		25/176			C	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001289	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003145	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000112	OMIM:277400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003223	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000276	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002013	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000790	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0002092	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0031258	OMIM:277400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001919	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0040126	PMID:29302025	PCS		0/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001518	PMID:29302025	PCS		1/3			P	HPO:probinson[2024-03-16]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0012120	OMIM:277400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000348	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0000505	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0003658	PMID:29302025	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001873	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:277400	Methylmalonic aciduria and homocystinuria, cblC type		HP:0001875	OMIM:277400	IEA					P	HPO:iea[2009-02-17]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0001298	OMIM:618230	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0002751	PMID:14729820	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0002015	OMIM:618230	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0003621	PMID:14729820	PCS		1/1			C	HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0001332	OMIM:618230	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0002530	PMID:14729820	PCS		1/1			P	HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0025258	PMID:14729820	PCS		1/1			P	HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0002151	OMIM:618230	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0002273	OMIM:618230	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0001290	OMIM:618230	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0002490	PMID:14729820	PCS		1/1			P	HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0002093	OMIM:618230	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0011923	PMID:14729820	PCS		1/1			P	HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0000007	PMID:14729820	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0000543	PMID:14729820	PCS		1/1			P	HPO:probinson[2022-10-19]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0001733	OMIM:618230	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618230	Mitochondrial complex I deficiency, nuclear type 8		HP:0003128	OMIM:618230	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611572	Otosclerosis 7		HP:0000362	PMID:16168495	PCS					P	HPO:iea[2009-02-17];HP:probinson[2018-11-22]
OMIM:611572	Otosclerosis 7		HP:0000365	PMID:16168495	PCS					P	HPO:skoehler[2010-06-20];HP:probinson[2018-11-22]
OMIM:611572	Otosclerosis 7		HP:0040121	PMID:16168495	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:611572	Otosclerosis 7		HP:0011474	PMID:16168495	PCS	HP:0011463				P	HPO:lccarmody[2018-10-04]
OMIM:611572	Otosclerosis 7		HP:0000405	PMID:16168495	PCS	HP:0011462				P	HPO:lccarmody[2018-10-04]
OMIM:611572	Otosclerosis 7		HP:0001730	PMID:16168495	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:611572	Otosclerosis 7		HP:0000006	PMID:16168495	PCS					I	HPO:iea[2009-02-17];HP:probinson[2018-11-22]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0002179	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0001298	OMIM:610678	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0000252	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0002376	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0002151	OMIM:610678	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0002240	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0003593	OMIM:610678	TAS					C	HPO:skoehler[2017-07-13]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0000639	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0000007	PMID:17160893	TAS					I	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0001987	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0001319	OMIM:610678	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0002878	OMIM:610678	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0001522	PMID:17160893	TAS					C	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0001511	OMIM:610678	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0001257	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0002415	OMIM:610678	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0001942	PMID:17160893	TAS					P	HPO:probinson[2013-01-09]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0002126	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:610678	Combined oxidative phosphorylation deficiency 4		HP:0003128	PMID:17160893	TAS					P	HPO:probinson[2013-04-01]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001298	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001254	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0003676	PMID:10330338	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-09]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0002376	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001332	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001250	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0011968	PMID:10330338	PCS		1/2			P	HPO:probinson[2023-06-09]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001260	PMID:10330338	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-09]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0002572	PMID:10330338	PCS		1/2			P	HPO:probinson[2023-06-09]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001251	PMID:10330338	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-09]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0002240	OMIM:618224	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001290	OMIM:618224	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0002071	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0002093	OMIM:618224	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0003819	PMID:10330338	PCS		2/2			C	HPO:probinson[2023-06-09]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0007256	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0000007	PMID:10330338	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-09]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001942	OMIM:618224	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618224	Mitochondrial complex I deficiency, nuclear type 3		HP:0001347	OMIM:618224	IEA					P	HPO:skoehler[2019-02-15]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0100502	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0003621	PMID:32276275	PCS		1/1			C	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0004851	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0001981	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0002904	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0002160	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0000007	PMID:32276275	PCS					I	HPO:probinson[2021-05-31];HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0025435	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0003281	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0004802	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0031688	PMID:32276275	PCS		1/1			P	HPO:probinson[2021-05-31]
OMIM:601775	Megaloblastic anemia, folate-responsive		HP:0004821	PMID:32276275	PCS	HP:0011462	1/1			P	HPO:probinson[2021-05-31]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0003236	OMIM:616209	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0010628	OMIM:616209	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0003200	PMID:25193783	PCS					P	HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0004322	PMID:25193783	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0011924	PMID:25193783	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0002151	OMIM:616209	TAS					P	HPO:skoehler[2015-02-22]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0011463	PMID:25193783	PCS					C	HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0008314	PMID:25193783	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0008347	PMID:25193783	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0000006	PMID:25193783	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0003677	PMID:25193783	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0003546	PMID:25193783	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-27]
OMIM:616209	Myopathy, isolated mitochondrial, autosomal dominant		HP:0003722	PMID:25193783	PCS					P	HPO:skoehler[2015-02-22];HPO:probinson[2022-08-27]
OMIM:144700	Renal cell carcinoma, nonpapillary		HP:0005584	OMIM:144700	TAS					P	HPO:probinson[2013-03-31]
OMIM:144700	Renal cell carcinoma, nonpapillary		HP:0003745	OMIM:144700	TAS					I	HPO:iea[2014-05-24]
OMIM:613371	Spinocerebellar ataxia 30		HP:0003587	OMIM:613371	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613371	Spinocerebellar ataxia 30		HP:0000640	OMIM:613371	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613371	Spinocerebellar ataxia 30		HP:0001272	OMIM:613371	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613371	Spinocerebellar ataxia 30		HP:0001260	OMIM:613371	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613371	Spinocerebellar ataxia 30		HP:0003581	OMIM:613371	TAS					C	HPO:skoehler[2015-12-30]
OMIM:613371	Spinocerebellar ataxia 30		HP:0001251	OMIM:613371	IEA					P	HPO:skoehler[2015-01-21]
OMIM:613371	Spinocerebellar ataxia 30		HP:0007338	OMIM:613371	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613371	Spinocerebellar ataxia 30		HP:0000006	OMIM:613371	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613371	Spinocerebellar ataxia 30		HP:0003677	OMIM:613371	TAS					C	HPO:skoehler[2012-10-17]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0002047	OMIM:145600	TAS					P	HPO:probinson[2009-02-17]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0003236	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0003198	OMIM:145600	TAS					P	HPO:probinson[2009-02-17]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0002153	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0009045	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0011440	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0002905	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0001945	OMIM:154275	TAS					P	HPO:skoehler[2014-01-28]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0003558	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0011439	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0000006	OMIM:154275	TAS					I	HPO:skoehler[2015-12-30]
OMIM:154275	Malignant hyperthermia, susceptibility to, 2		HP:0003128	OMIM:145600	TAS					P	HPO:probinson[2012-03-18]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0003774	PMID:22019273	PCS		1/2			P	HPO:skoehler[2013-05-29];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000286	PMID:22019273	PCS		1/2			P	HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0003577	PMID:22019273	PCS		2/2			C	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000662	PMID:22019273	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000540	PMID:22019273	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0004322	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000463	PMID:22019273	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0004442	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0001805	PMID:22019273	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000319	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0010174	PMID:22019273	PCS		2/2			P	HPO:probinson[2013-04-07];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0009882	PMID:22019273	PCS					P	HPO:probinson[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000679	PMID:22019273	PCS		1/2			P	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:6001070	PMID:28621010	PCS					P	HPO:probinson[2024-08-03]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0006532	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0005528	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000774	PMID:22019273	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000411	PMID:22019273	PCS		1/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000510	PMID:22019273	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000973	PMID:22019273	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0001385	PMID:22019273	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000233	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000293	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0001382	PMID:22019273	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0033036	PMID:22019273	PCS		0/2			P	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0010554	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0008081	PMID:22019273	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000767	PMID:22019273	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000007	PMID:22019273	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0000505	PMID:22019273	PCS		2/2			P	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0001319	PMID:22019273	PCS	HP:0003623	1/2			P	HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0002007	PMID:22019273	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-20]
OMIM:614378	Cranioectodermal dysplasia 4		HP:0009836	PMID:22019273	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-07-20]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0002650	PMID:28323974;PMID:26911354	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-04-21];HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0000365	PMID:26911354	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0002980	PMID:28323974	PCS	HP:0030674	2/8			P	HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0002980	PMID:26911354	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0004322	PMID:28323974;PMID:26911354	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-04-21];HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0030674	PMID:28323974	PCS		2/8			C	HPO:probinson[2022-03-31]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0003100	PMID:26911354	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0003155	PMID:26911354	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0001263	PMID:28323974	PCS		2/8			P	HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0000592	PMID:28323974;PMID:26911354	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-04-21];HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0004363	PMID:26911354	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0003593	PMID:28323974	PCS		2/8			C	HPO:probinson[2022-03-31];HPO:probinson[2022-03-31]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0001270	PMID:28323974	PCS		2/8			P	HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0031425	PMID:26911354	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0000939	PMID:26911354	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0000407	PMID:28323974	PCS		2/8			P	HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0011463	PMID:28323974;PMID:26911354	PCS		4/11			C	HPO:probinson[2022-03-31];ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0000938	PMID:28323974	PCS		8/8			P	HPO:skoehler[2015-08-25];HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0000007	PMID:28323974	PCS					I	HPO:skoehler[2015-08-25];HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0002757	PMID:28323974;PMID:26911354	PCS		8/9			P	HPO:skoehler[2015-08-25];HP:probinson[2019-05-10];ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0000703	PMID:26911354	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0002659	PMID:28323974	PCS					P	HPO:skoehler[2015-08-25];HP:probinson[2019-05-10]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0002645	PMID:26911354	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0002753	PMID:26911354	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:615066	Osteogenesis imperfecta, type XIV		HP:0003623	PMID:28323974;PMID:26911354	PCS		2/11			C	HPO:probinson[2022-03-31];ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:189000	Toe, fifth, number of phalanges in		HP:0000924	OMIM:189000	IEA					P	HPO:iea[2009-02-17]
OMIM:189000	Toe, fifth, number of phalanges in		HP:0000006	OMIM:189000	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:605275	Noonan syndrome 2		HP:0001133	PMID:30368668	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0000286	PMID:29469822;PMID:30368668	PCS		11/27			P	HPO:probinson[2021-05-21];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0007517	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001212	PMID:29469822	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000486	PMID:30368668	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0001134	PMID:29469822	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0004322	PMID:29469822;PMID:30368668	PCS		14/24			P	HPO:probinson[2021-05-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0001250	PMID:30368668	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0003593	PMID:29469822;PMID:30368668	PCS		7/22			C	ORCID:0000-0002-0736-9199[2024-10-02];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0004482	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0045075	PMID:30368668	PCS		5/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000914	PMID:29469822	PCS		12/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000957	PMID:30368668	PCS		1/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0011463	PMID:29469822	PCS		1/18			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001928	PMID:30368668	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0011461	PMID:30368668	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0001647	PMID:29469822	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000316	PMID:29469822;PMID:30368668	PCS		13/22			P	HPO:probinson[2021-05-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000953	PMID:30368668	PCS		4/4			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001643	PMID:30368668	PCS		1/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000476	PMID:29469822	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001642	PMID:29469822;PMID:30368668	PCS		4/27			P	HPO:probinson[2021-05-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001249	PMID:30368668	PCS		4/6			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000358	PMID:29469822	PCS		14/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000995	PMID:29469822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0003623	PMID:29469822	PCS		1/18			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000175	PMID:30368668	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0000494	PMID:29469822;PMID:30368668	PCS		13/23			P	HPO:probinson[2021-05-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0003764	PMID:30368668	PCS		2/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001263	PMID:29469822;PMID:30368668	PCS		9/15			P	ORCID:0000-0002-0736-9199[2024-10-02];HPO:skoehler[2019-02-15];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0011800	PMID:29469822	PCS		9/14			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0010880	PMID:29469822;PMID:30368668	PCS		6/11			P	HPO:probinson[2021-05-21];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0009891	PMID:30368668	PCS		5/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000767	PMID:29469822;PMID:30368668	PCS		8/27			P	HPO:probinson[2021-05-21];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000766	PMID:29469822	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000007	PMID:29469822	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000964	PMID:30368668	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0000648	PMID:30368668	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0000768	PMID:29469822;PMID:30368668	PCS		3/27			P	HPO:probinson[2021-05-21];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000006	PMID:30368668	PCS					I	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0000369	PMID:29469822;PMID:30368668	PCS		20/23			P	HPO:probinson[2021-05-21];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0000962	PMID:30368668	PCS		4/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001655	PMID:29469822;PMID:30368668	PCS		4/26			P	ORCID:0000-0002-0736-9199[2024-10-02];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001034	PMID:29469822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000341	PMID:30368668	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0003577	PMID:29469822	PCS		1/18			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000343	PMID:29469822	PCS		4/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000463	PMID:29469822	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0030674	PMID:29469822	PCS		11/18			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0002162	PMID:29469822	PCS		10/20			P	HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0001790	PMID:29469822;PMID:30368668	PCS		2/24			P	ORCID:0000-0002-0736-9199[2024-10-02];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0011636	PMID:30368668	PCS		1/6			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001909	PMID:29469822	PCS		2/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001629	PMID:29469822;PMID:30368668	PCS		6/27			P	HPO:probinson[2021-05-21];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0006695	PMID:29469822	PCS		1/20			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000218	PMID:29469822;PMID:30368668	PCS		5/26			P	HPO:probinson[2021-05-21];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0006610	PMID:29469822	PCS		3/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0005989	PMID:29469822	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000974	PMID:30368668	PCS		2/7			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0004415	PMID:29469822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0002212	PMID:29469822;PMID:30368668	PCS		8/21			P	HPO:probinson[2021-05-21];HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0000396	PMID:29469822	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000154	PMID:29469822	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001561	PMID:29469822	PCS		6/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0002650	PMID:30368668	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0000431	PMID:29469822	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0025676	PMID:30368668	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-02]
OMIM:605275	Noonan syndrome 2		HP:0005684	PMID:29469822	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001680	OMIM:605275	IEA					P	HPO:skoehler[2019-02-15]
OMIM:605275	Noonan syndrome 2		HP:0000470	PMID:29469822;PMID:30368668	PCS		12/27			P	HPO:probinson[2021-05-21];HPO:skoehler[2019-09-07];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0005280	PMID:29469822	PCS		4/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001639	PMID:29469822;PMID:30368668	PCS		19/25			P	HPO:probinson[2021-05-21];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000506	PMID:29469822	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001718	OMIM:605275	IEA					P	HPO:skoehler[2019-02-15]
OMIM:605275	Noonan syndrome 2		HP:0000508	PMID:29469822;PMID:30368668	PCS		10/26			P	HPO:probinson[2021-05-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0002804	PMID:29469822	PCS		2/20			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001638	PMID:29469822	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000307	PMID:29469822	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0002967	PMID:30368668	PCS		2/6			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0006721	PMID:29469822	PCS		3/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0001631	PMID:29469822;PMID:30368668	PCS		7/8			P	HPO:probinson[2021-05-21];HPO:probinson[2021-05-21];HPO:probinson[2024-03-26]
OMIM:605275	Noonan syndrome 2		HP:0000465	PMID:29469822;PMID:30368668	PCS		7/10			P	ORCID:0000-0002-0736-9199[2024-10-02];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:605275	Noonan syndrome 2		HP:0000028	PMID:29469822;PMID:30368668	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-10-02];HPO:skoehler[2019-04-18];HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0000347	PMID:29469822	PCS		9/13			P	HPO:probinson[2021-05-21]
OMIM:605275	Noonan syndrome 2		HP:0001634	PMID:29469822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000582	PMID:24721225	PCS		3/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000486	PMID:24721225	PCS		3/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000750	PMID:24721225	PCS		7/7			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0001250	PMID:24721225	PCS		1/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000193	PMID:24721225	PCS		1/8			P	HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0001263	PMID:24721225	PCS					P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0001252	PMID:24721225	PCS		3/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000272	PMID:24721225	PCS		3/8			P	HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0001270	PMID:24721225	PCS		6/6			P	HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0001419	PMID:24721225	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000805	PMID:24721225	PCS		4/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0001417	PMID:15185169	PCS		14/14	MALE		I	HPO:skoehler[2013-02-16];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000218	PMID:24721225	PCS		3/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0000774	PMID:24721225	PCS		3/8			P	HPO:skoehler[2014-07-11];HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0007018	PMID:24721225	PCS		3/6			P	HPO:probinson[2021-09-26]
OMIM:300850	Intellectual developmental disorder, X-linked 90		HP:0001249	PMID:15185169;PMID:24721225	PCS		18/18			P	HPO:skoehler[2013-01-09];HPO:probinson[2021-09-26]
OMIM:617671	Helix syndrome		HP:0003577	PMID:28686597	PCS		13/13			C	HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0000970	PMID:28686597	IEA	HP:0003577	13/13			P	HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0002046	PMID:28686597	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0000083	OMIM:617671	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617671	Helix syndrome		HP:0000958	OMIM:617671	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617671	Helix syndrome		HP:0001959	OMIM:617671	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617671	Helix syndrome		HP:0002918	PMID:28686597	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0000217	PMID:28686597	PCS		13/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0000007	PMID:28686597	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0000843	PMID:28686597	PCS		2/2			P	HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0002900	OMIM:617671	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617671	Helix syndrome		HP:0000966	OMIM:617671	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617671	Helix syndrome		HP:0000103	OMIM:617671	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617671	Helix syndrome		HP:0000787	PMID:28686597	PCS	HP:0003621	4/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-13]
OMIM:617671	Helix syndrome		HP:0003127	OMIM:617671	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617671	Helix syndrome		HP:0000522	PMID:28686597	PCS		13/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-13]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0000252	PMID:34450031	PCS		4/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0002136	PMID:34450031	PCS		2/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0002540	PMID:34450031	PCS		2/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0002188	PMID:34450031	PCS		2/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0001250	PMID:34450031	PCS		2/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0001263	PMID:34450031	PCS		6/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0003593	PMID:34450031	PCS		1/4			C	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0032046	PMID:34450031	PCS		1/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0033725	PMID:34450031	PCS		2/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0011463	PMID:34450031	PCS		3/4			C	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0000938	PMID:34450031	PCS		5/5			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0002757	PMID:34450031	PCS		2/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0001257	PMID:34450031	PCS		4/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0000006	PMID:34450031	PCS					I	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0001249	PMID:34450031	PCS		3/4			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0001622	PMID:34450031	PCS		3/6			P	HPO:probinson[2022-08-14]
OMIM:619884	Osteoporosis, childhood- or juvenile-onset, with developmental delay		HP:0009879	PMID:34450031	PCS		2/6			P	HPO:probinson[2022-08-14]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0003621	PMID:12021217	PCS		3/3			C	HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001663	OMIM:608751	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001695	OMIM:608751	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0010872	PMID:12021217	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0012664	PMID:12021217	PCS		0/1			P	HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001639	PMID:8673105	PCS		13/13			P	HPO:probinson[2013-03-05];HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0031295	PMID:12021217	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0000007	PMID:12021217	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001723	PMID:12021217	PCS					P	HPO:probinson[2013-03-05]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001635	OMIM:608751	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001712	PMID:12021217	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0006685	PMID:12021217	PCS					P	HPO:probinson[2013-03-05]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001962	OMIM:608751	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0000006	PMID:8673105	PCS					I	HPO:probinson[2013-03-05];HPO:probinson[2022-07-04]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0001645	OMIM:608751	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608751	Cardiomyopathy, familial hypertrophic, 8		HP:0002875	OMIM:608751	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614350	Colorectal cancer, hereditary nonpolyposis, type 5		HP:0002894	PMID:9354786	PCS					P	HPO:probinson[2022-11-28]
OMIM:614350	Colorectal cancer, hereditary nonpolyposis, type 5		HP:0006716	PMID:9354786	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-28]
OMIM:614350	Colorectal cancer, hereditary nonpolyposis, type 5		HP:0100615	PMID:9354786	PCS					P	HPO:probinson[2022-11-28]
OMIM:614350	Colorectal cancer, hereditary nonpolyposis, type 5		HP:0003581	PMID:9354786	PCS					C	HPO:probinson[2022-11-28]
OMIM:614350	Colorectal cancer, hereditary nonpolyposis, type 5		HP:0003829	PMID:9354786	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-28]
OMIM:614350	Colorectal cancer, hereditary nonpolyposis, type 5		HP:0012114	PMID:9354786	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-11-28]
OMIM:614350	Colorectal cancer, hereditary nonpolyposis, type 5		HP:0000006	PMID:9354786	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-11-28]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0007814	PMID:31903486	PCS		1/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0003577	PMID:31345061	PCS		2/2			C	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0025169	PMID:31903486	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0003593	PMID:31903486	PCS		2/2			C	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0030609	PMID:31345061;PMID:31903486	PCS		4/4			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0030329	PMID:31345061	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0200070	PMID:31903486	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0000639	PMID:31345061	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0500182	PMID:31345061;PMID:31903486	PCS		4/4			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0008499	PMID:31345061	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0007994	PMID:31345061	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0007401	PMID:31903486	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0007843	PMID:31345061	PCS		2/2			P	HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0000006	PMID:31903486	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2021-06-30]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0001634	OMIM:145350	TAS					P	HPO:skoehler[2009-02-17]
OMIM:145350	Hypotaurinemic retinal degeneration and cardiomyopathy		HP:0001644	PMID:31903486	PCS		2/2			P	HPO:skoehler[2013-06-11];HPO:probinson[2021-06-30]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0001265	PMID:17572665	PCS					P	HPO:probinson[2013-04-01]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0003676	OMIM:611228	TAS					C	HPO:skoehler[2015-12-30]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0003431	OMIM:611228	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0001288	OMIM:611228	TAS					P	HPO:skoehler[2014-10-06]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0005684	PMID:17572665	PCS					P	HPO:probinson[2013-04-01]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0003383	OMIM:611228	TAS					P	HPO:skoehler[2014-10-06]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0002460	PMID:17572665	PCS					P	HPO:probinson[2013-04-01]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0001284	OMIM:611228	TAS					P	HPO:skoehler[2014-10-06]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0001270	OMIM:611228	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0007182	PMID:17572665	PCS					P	HPO:probinson[2013-04-01]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0003828	OMIM:611228	TAS					M	HPO:skoehler[2015-12-30]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0000007	PMID:17572665	PCS					I	HPO:probinson[2013-01-09]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0002936	OMIM:611228	TAS					P	HPO:skoehler[2014-10-06]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0006466	OMIM:611228	TAS					P	HPO:skoehler[2014-10-06]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0002359	OMIM:611228	TAS					P	HPO:skoehler[2014-10-06]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0000762	PMID:17572665	PCS					P	HPO:probinson[2013-04-01]
OMIM:611228	Charcot-Marie-Tooth disease, type 4J		HP:0003447	PMID:17572665	PCS					P	HPO:probinson[2013-04-01]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0004325	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000341	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001355	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0005676	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000023	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0004322	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001156	OMIM:600325	TAS					P	HPO:skoehler[2014-11-26]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001252	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000316	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000218	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0030084	OMIM:600325	TAS					P	HPO:skoehler[2014-09-21]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000256	OMIM:600325	TAS					P	HPO:skoehler[2013-10-22]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000358	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000677	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0002236	OMIM:600325	TAS					P	HPO:skoehler[2013-06-03]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001166	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0002553	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000252	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000175	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001263	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0045025	OMIM:600325	TAS					P	HPO:skoehler[2014-11-27]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0009473	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0009891	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001537	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001999	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000007	OMIM:600325	IEA					I	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001511	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0002007	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0001159	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0002943	OMIM:600325	IEA					P	HPO:iea[2009-02-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0009778	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000028	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000369	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000347	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600325	Aminopterin syndrome sine aminopterin		HP:0000248	OMIM:600325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0003236	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001410	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0004322	OMIM:608779	IEA					P	HPO:skoehler[2019-04-18]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001250	PMID:17356545;PMID:15107842	PCS		4/5			P	HPO:skoehler[2019-02-15];HP:probinson[2019-02-17];HPO:probinson[2023-01-28];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000160	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0010808	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0003196	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001252	PMID:17356545	PCS		3/3			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0002020	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001290	PMID:15107842	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0012745	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0012301	PMID:17356545;PMID:15107842	PCS		4/4			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000319	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0012471	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000998	PMID:17356545	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001522	PMID:17356545;PMID:15107842	PCS		5/5			C	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000278	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000952	PMID:15107842	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001265	OMIM:608779	IEA					P	HPO:skoehler[2019-04-18]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000011	OMIM:608779	IEA					P	HPO:skoehler[2019-04-18]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000253	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0003202	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0031956	PMID:17356545	PCS		3/3			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0002079	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0011968	PMID:17356545	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000294	PMID:17356545	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0012736	OMIM:608779	TAS					P	HP:probinson[2019-02-17]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001181	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0010557	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0007392	PMID:17356545;PMID:15107842	PCS		5/5			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000407	PMID:17356545	PCS		1/3			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0011451	PMID:17356545	PCS		2/3			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000007	PMID:15107842	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000369	PMID:15107842	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000126	PMID:17356545	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000445	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000341	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000582	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0003577	PMID:17356545;PMID:15107842	PCS		5/5			C	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001272	PMID:17356545	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0002240	PMID:15107842	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0012448	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0012768	PMID:15107842	PCS		2/2			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0031964	PMID:17356545	PCS		1/3			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001508	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0002719	PMID:15107842	PCS		1/2			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0011682	PMID:17356545	PCS		2/3			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001943	PMID:17356545	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001744	PMID:15107842	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0002059	PMID:17356545	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001684	PMID:17356545	PCS		2/3			P	HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0003186	OMIM:608779	IEA					P	HPO:skoehler[2019-04-18]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000470	PMID:17356545;PMID:15107842	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0002093	OMIM:608779	IEA					P	HPO:skoehler[2019-04-18]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001635	PMID:15107842	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001511	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0001510	PMID:17356545	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0000347	PMID:17356545;PMID:15107842	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-28];HPO:probinson[2023-01-28]
OMIM:608779	Congenital disorder of glycosylation, type IIe		HP:0004425	OMIM:608779	IEA					P	HPO:skoehler[2019-02-15]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0004303	PMID:38413582	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0030237	PMID:38366623	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003577	PMID:38413582	PCS		8/18			C	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0030234	PMID:38366623;PMID:38413582	PCS		20/22			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0001272	PMID:38413582	PCS		5/9			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003551	PMID:38366623;PMID:38413582	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003593	PMID:38413582	PCS		1/18			C	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0001270	PMID:38413582	PCS		15/18			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003391	PMID:38413582	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0030319	PMID:38366623	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0100297	PMID:38413582	PCS		9/9			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0007021	PMID:38413582	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0011463	PMID:38366623;PMID:38413582	PCS		10/23			C	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003707	PMID:38413582	PCS		6/17			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0009046	PMID:38366623	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0000519	PMID:38413582	PCS		6/18			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0008994	PMID:38366623;PMID:38413582	PCS		23/23			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003307	PMID:38366623;PMID:38413582	PCS		7/21			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0020202	PMID:38366623	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0002317	PMID:38413582	PCS		7/7			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003327	PMID:38413582	PCS		16/18			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003306	PMID:38366623;PMID:38413582	PCS		3/17			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0008997	PMID:38366623;PMID:38413582	PCS		23/23			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0030227	PMID:38366623	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0000252	PMID:38413582	PCS		1/16			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003621	PMID:38366623;PMID:38413582	PCS		4/23			C	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0002650	PMID:38413582	PCS		11/16			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003200	PMID:38413582	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0008959	PMID:38366623;PMID:38413582	PCS		17/21			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0001382	PMID:38366623	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003121	PMID:38413582	PCS		14/18			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0001263	PMID:38366623;PMID:38413582	PCS		2/7			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0001284	PMID:38413582	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0002093	PMID:38413582	PCS		11/18			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0002091	PMID:38366623	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0008180	PMID:38366623	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0034392	PMID:38366623	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0009053	PMID:38366623;PMID:38413582	PCS		21/23			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0000407	PMID:38413582	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0001558	PMID:38413582	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0000007	PMID:38413582	PCS					I	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0001638	PMID:38366623;PMID:38413582	PCS		0/19			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0002505	PMID:38366623;PMID:38413582	PCS		14/23			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0200012	PMID:38413582	PCS		3/7			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0034391	PMID:38366623	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:620793	Muscular dystrophy, limb-girdle, autosomal recessive 29		HP:0003458	PMID:38366623;PMID:38413582	PCS		12/12			P	ORCID:0000-0002-0736-9199[2025-01-06]
OMIM:616221	Amelogenesis imperfecta, type IH		HP:0000705	PMID:24305999	PCS					P	HPO:probinson[2015-04-24]
OMIM:616221	Amelogenesis imperfecta, type IH		HP:0009102	PMID:24305999;OMIM:616221	PCS		12/20			P	HPO:probinson[2015-04-24];HPO:skoehler[2015-08-16]
OMIM:616221	Amelogenesis imperfecta, type IH		HP:0006297	PMID:24305999	PCS					P	HPO:probinson[2015-04-24]
OMIM:616221	Amelogenesis imperfecta, type IH		HP:0006286	PMID:24305999	PCS					P	HPO:probinson[2015-04-24]
OMIM:616221	Amelogenesis imperfecta, type IH		HP:0000007	PMID:24305999	PCS					I	HPO:probinson[2015-04-24]
OMIM:616221	Amelogenesis imperfecta, type IH		HP:0009722	PMID:24319098	PCS					P	HPO:probinson[2015-04-24]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0003621	PMID:20806400	PCS		2/3			C	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0033383	PMID:20806400	PCS		3/3			P	HPO:probinson[2021-02-13]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0001288	PMID:20806400	PCS					P	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0009053	PMID:20806400	PCS					P	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0003487	PMID:20806400	PCS		3/3			P	HPO:probinson[2021-01-02];HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0001761	PMID:20806400	PCS					P	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0003581	PMID:20806400	PCS		1/3			C	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0003393	PMID:20806400	PCS					P	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0002359	PMID:20806400	PCS	HP:0003581				P	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0000006	PMID:20806400	PCS					I	HPO:probinson[2021-01-02];HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0008944	PMID:20806400	PCS					P	HPO:probinson[2021-01-02]
OMIM:619112	Neuropathy, distal hereditary motor, type VC		HP:0010875	PMID:20806400	PCS		3/3			P	HPO:probinson[2021-01-02];HPO:probinson[2021-01-02]
OMIM:113670	Breast, unilateral giant		HP:0001470	OMIM:113670	IEA					I	HPO:iea[2009-02-17]
OMIM:113670	Breast, unilateral giant		HP:0000765	OMIM:113670	IEA					P	HPO:iea[2009-02-17]
OMIM:615728	Pachyonychia congenita 4		HP:0012035	PMID:9618173	PCS					P	HPO:skoehler[2015-09-12];HPO:probinson[2022-04-11]
OMIM:615728	Pachyonychia congenita 4		HP:0008404	PMID:9618173	PCS					P	HPO:skoehler[2015-09-12];HPO:probinson[2022-04-11]
OMIM:615728	Pachyonychia congenita 4		HP:0000982	PMID:9618173	PCS					P	HPO:skoehler[2015-09-12];HPO:probinson[2022-04-11]
OMIM:615728	Pachyonychia congenita 4		HP:0000006	PMID:9618173	PCS					I	HPO:skoehler[2015-09-12];HPO:probinson[2022-04-11]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0001265	OMIM:614436	TAS					P	HPO:skoehler[2013-08-18]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0003378	OMIM:614436	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0003376	OMIM:614436	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0003431	OMIM:614436	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0001761	OMIM:614436	TAS					P	HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0003693	OMIM:614436	TAS					P	HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0002460	OMIM:614436	TAS					P	HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0001284	OMIM:614436	TAS					P	HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0002380	OMIM:614436	TAS					P	HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0003829	OMIM:614436	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0040078	OMIM:614436	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0009027	OMIM:614436	TAS					P	HPO:skoehler[2013-08-18]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0000007	OMIM:614436;PMID:20865121	PCS		20/20			I	HP:probinson[2018-04-29];HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0002936	OMIM:614436	TAS					P	HPO:skoehler[2013-08-18]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0030051	OMIM:614436	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0006886	OMIM:614436	TAS					P	HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0000006	OMIM:614436	TAS					I	HPO:skoehler[2013-08-18]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0003677	PMID:22012984	TAS					C	HPO:skoehler[2013-08-18]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0000764	OMIM:614436	TAS					P	HPO:probinson[2013-08-10]
OMIM:614436	Charcot-Marie-Tooth disease, axonal, type 2P		HP:0001765	OMIM:614436	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:604625	Tooth agenesis, selective, 3		HP:0001595	PMID:16333316	PCS		0/5			P	HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0003621	PMID:10615120	PCS					C	HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0001231	PMID:16333316	PCS		0/5			P	HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0000970	PMID:16333316	PCS		0/5			P	HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0000691	OMIM:604625	TAS		HP:0040283			P	HPO:skoehler[2015-08-05]
OMIM:604625	Tooth agenesis, selective, 3		HP:0011055	PMID:10615120	PCS		16/16			P	HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0011121	PMID:16333316	PCS		0/5			P	HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0012225	PMID:10615120	PCS		0/16			P	HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0000006	PMID:10615120	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-03-17]
OMIM:604625	Tooth agenesis, selective, 3		HP:0000677	PMID:10615120	PCS		16/16			P	HPO:probinson[2022-03-17];HPO:probinson[2013-02-22];HPO:probinson[2022-03-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0003236	PMID:16282978;PMID:18285827	PCS		23/28			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0000486	PMID:16282978;PMID:18285827	PCS		24/27			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0004322	PMID:16282978;PMID:18285827	PCS		18/30			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001371	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0003198	PMID:16282978	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001272	PMID:18285827	PCS		7/7			P	HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0002066	OMIM:248800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001252	PMID:16282978;PMID:18285827	PCS		29/29			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001251	PMID:16282978;PMID:18285827	PCS		29/29			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0003593	OMIM:248800;PMID:18285827	PCS		12/15			C	HPO:probinson[2023-02-12];HPO:skoehler[2012-10-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0010049	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0010743	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001508	OMIM:248800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0000815	PMID:16282978;PMID:18285827	PCS		19/21			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0000639	PMID:16282978;PMID:18285827	PCS		20/29			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0011463	PMID:18285827	PCS		3/5			C	HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0000519	PMID:16282978;PMID:18285827	PCS		30/30			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0008278	PMID:16282978	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0003805	OMIM:248800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001763	OMIM:248800	TAS					P	HPO:probinson[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001249	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0003323	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0003202	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0003687	OMIM:248800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0000252	PMID:16282978;PMID:18285827	PCS		2/28			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0002650	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0002673	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001260	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001263	PMID:16282978;PMID:18285827	PCS		29/29			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-12];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0002070	OMIM:248800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0002808	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0000007	PMID:16282978	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0002967	OMIM:248800	IEA					P	HPO:iea[2009-02-17]
OMIM:248800	Marinesco-Sjogren syndrome		HP:0001257	PMID:18285827	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:614422	Cataract, congenital, cerulean type, 5		HP:0000519	OMIM:614422	IEA					P	HPO:skoehler[2015-01-27]
OMIM:614422	Cataract, congenital, cerulean type, 5		HP:0000006	OMIM:614422	TAS					I	HPO:skoehler[2012-10-17]
OMIM:257920	3MC syndrome 1		HP:0001773	OMIM:257920	TAS					P	HPO:probinson[2013-04-08]
OMIM:257920	3MC syndrome 1		HP:0000365	PMID:21258343	PCS		5/6			P	HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0004443	OMIM:257920	IEA					P	HPO:iea[2012-02-24]
OMIM:257920	3MC syndrome 1		HP:0000260	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0003298	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0004440	OMIM:257920	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0000581	PMID:21258343;PMID:21035106	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0410030	PMID:21258343	PCS		4/6			P	HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0001629	OMIM:257920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257920	3MC syndrome 1		HP:0000316	PMID:21258343;PMID:21035106	PCS		6/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0000678	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0008897	PMID:21258343	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0001769	OMIM:257920	TAS					P	HPO:probinson[2013-04-08]
OMIM:257920	3MC syndrome 1		HP:0000537	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0001643	OMIM:257920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257920	3MC syndrome 1		HP:0002678	PMID:21258343	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0002558	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0006216	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0001249	PMID:21258343	PCS		0/6			P	HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0002974	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0002553	PMID:21258343;PMID:21035106	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0001540	PMID:21258343	PCS		0/6			P	HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0000593	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000175	PMID:21258343	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0000252	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000494	PMID:21035106	PCS		3/3			P	HPO:probinson[2023-02-21]
OMIM:257920	3MC syndrome 1		HP:0000496	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0004298	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:6000808	PMID:16096999	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:257920	3MC syndrome 1		HP:0009891	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000506	PMID:21035106	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:257920	3MC syndrome 1		HP:0000508	PMID:21258343;PMID:21035106	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0002825	PMID:21258343;PMID:21035106	PCS		7/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21];HPO:probinson[2023-02-27]
OMIM:257920	3MC syndrome 1		HP:0000524	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000007	PMID:21035106	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:257920	3MC syndrome 1		HP:0001539	PMID:21035106	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:257920	3MC syndrome 1		HP:0004209	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0009237	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000405	PMID:21035106	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:257920	3MC syndrome 1		HP:0000664	PMID:21035106	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:257920	3MC syndrome 1		HP:0001631	OMIM:257920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257920	3MC syndrome 1		HP:0001510	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000960	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000501	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:257920	3MC syndrome 1		HP:0000204	PMID:21035106	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:257920	3MC syndrome 1		HP:0000126	OMIM:257920	IEA					P	HPO:iea[2009-02-17]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0001792	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0002155	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0030731	OMIM:610644	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0000771	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0003124	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0000062	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0011838	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0003241	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0012118	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0025080	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0012861	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0000007	OMIM:610644	TAS					I	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0007410	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0008665	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0008734	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0006357	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0008404	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0000047	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610644	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal		HP:0000982	OMIM:610644	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600457	Hypertrichosis, anterior cervical		HP:0004535	OMIM:600457	IEA					P	HPO:iea[2009-02-17]
OMIM:618218	Baker-Gordon syndrome		HP:0000286	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0002487	PMID:30107533	PCS		1/11			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0002540	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0000486	PMID:30107533	PCS		2/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0001332	PMID:30107533	PCS		3/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0003196	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0001251	PMID:30107533	PCS		1/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0002020	PMID:30107533	PCS		4/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0003593	PMID:30107533	PCS		11/11			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0005274	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0000639	PMID:30107533	PCS		5/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0000319	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0000733	PMID:30107533	PCS		4/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0000219	OMIM:618218	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618218	Baker-Gordon syndrome		HP:0001760	OMIM:618218	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618218	Baker-Gordon syndrome		HP:0002353	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0002650	OMIM:618218	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618218	Baker-Gordon syndrome		HP:0001344	PMID:30107533	PCS		9/11			P	HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0001266	PMID:30107533	PCS		2/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0031936	PMID:30107533	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0011968	PMID:30107533	PCS		2/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0001382	OMIM:618218	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618218	Baker-Gordon syndrome		HP:0001263	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0011445	PMID:30107533	PCS		1/11			P	HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0100660	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0010535	PMID:30107533	PCS		1/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0000348	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618218	Baker-Gordon syndrome		HP:0001319	OMIM:618218	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618218	Baker-Gordon syndrome		HP:0100716	PMID:30107533	PCS		9/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0000505	OMIM:618218	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618218	Baker-Gordon syndrome		HP:0000006	PMID:30107533	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-13]
OMIM:618218	Baker-Gordon syndrome		HP:0004305	OMIM:618218	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0002983	PMID:27666822	PCS		1/2		HP:0012828	P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000343	PMID:27666822	PCS	HP:0003577	1/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0002089	PMID:27666822	PCS					P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0005257	PMID:27666822	PCS					P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0001156	OMIM:617895	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000062	OMIM:617895	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0001290	PMID:27666822	PCS		2/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0004482	PMID:27666822	PCS		2/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0001629	PMID:27666822	PCS		1/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0011220	OMIM:617895	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0002878	PMID:27666822	PCS					P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000895	PMID:27666822	PCS	HP:0003577	1/1			P	HP:probinson[2018-06-14]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000774	OMIM:617895	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000773	PMID:27666822	PCS		1/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0002098	PMID:27666822	PCS					P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0011800	PMID:27666822	PCS		1/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0005280	OMIM:617895	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0100259	PMID:27666822	PCS		1/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000946	PMID:27666822	PCS					P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000888	PMID:27666822	PCS					P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000007	PMID:27666822	PCS					I	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0001539	OMIM:617895	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000268	PMID:27666822	PCS		2/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0001159	OMIM:617895	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000520	OMIM:617895	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0002984	PMID:27666822	PCS					P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000369	PMID:27666822	PCS		1/2			P	HP:probinson[2018-05-12]
OMIM:617895	Short-Rib thoracic dysplasia 19 with or without polydactyly		HP:0000269	PMID:27666822	PCS		2/2			P	HP:probinson[2018-05-12]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0000164	OMIM:616553	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0000252	OMIM:616553	TAS					P	HPO:skoehler[2015-10-05]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0001321	OMIM:616553	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0001263	OMIM:616553	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0003581	PMID:25205116	PCS		3/3			C	HPO:probinson[2023-02-04]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0031413	PMID:25205116	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0001915	PMID:25205116	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-04]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0010450	OMIM:616553	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0000007	PMID:25205116	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0005528	PMID:25205116	PCS		2/3		HP:0003676	P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-04]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0001511	OMIM:616553	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0008404	OMIM:616553	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0002745	OMIM:616553	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0000006	OMIM:616553	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616553	Dyskeratosis congenita, autosomal dominant 6		HP:0001876	OMIM:616553	TAS					P	HPO:skoehler[2015-10-05]
OMIM:600331	Parc syndrome		HP:0002223	OMIM:600331	PCS		1/1			P	HPO:probinson[2009-02-17]
OMIM:600331	Parc syndrome		HP:0000561	OMIM:600331	PCS		1/1			P	HPO:probinson[2012-03-02]
OMIM:600331	Parc syndrome		HP:0000175	OMIM:600331	PCS		1/1			P	HPO:probinson[2009-02-17]
OMIM:600331	Parc syndrome		HP:0001596	OMIM:600331	PCS		1/1			P	HPO:probinson[2009-02-17]
OMIM:600331	Parc syndrome		HP:0000308	OMIM:600331	PCS		1/1			P	HPO:probinson[2009-02-17]
OMIM:600331	Parc syndrome		HP:0001029	OMIM:600331	PCS		1/1			P	HPO:probinson[2009-02-17]
OMIM:600331	Parc syndrome		HP:0000006	OMIM:600331	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:614344	Intellectual developmental disorder, autosomal recessive 23		HP:0000007	OMIM:614344	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614344	Intellectual developmental disorder, autosomal recessive 23		HP:0001270	OMIM:614344	TAS				HP:0012826	P	HPO:skoehler[2017-07-13]
OMIM:133239	Esophageal cancer, somatic		HP:0001442	OMIM:133239	IEA					I	HPO:skoehler[2019-02-22]
OMIM:133239	Esophageal cancer, somatic		HP:0011459	OMIM:133239	TAS					P	HPO:probinson[2021-07-16]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000343	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001057	PMID:23122588	PCS		4/4			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0004322	PMID:23122588	PCS		2/4			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0003196	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001274	PMID:23122588	PCS		2/4			P	HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0012448	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000316	OMIM:300887	TAS		HP:0040282			P	HPO:skoehler[2013-06-03]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0006610	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001423	PMID:23122588	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000358	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001249	PMID:23122588	PCS		2/4			P	HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000776	PMID:23122588	PCS		1/4			P	HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0002553	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000252	PMID:23122588	PCS		3/4			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0002079	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000331	OMIM:300887	TAS		HP:0040282			P	HPO:skoehler[2013-06-03]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001263	OMIM:300887	TAS		15/20			P	HPO:skoehler[2019-02-22];HPO:skoehler[2013-06-03]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0002092	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001636	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0007398	PMID:23122588	PCS		4/4			P	HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000348	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000568	PMID:23122588	PCS		0/4			P	HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000505	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001714	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000543	PMID:23122588	PCS		1/4			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001852	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0008404	PMID:23122588	PCS		1/4			P	HPO:probinson[2023-05-08]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0001631	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:300887	Linear skin defects with multiple congenital anomalies 2		HP:0000545	OMIM:300887	TAS		HP:0040283			P	HPO:skoehler[2013-05-07]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0001265	OMIM:243000	TAS		0/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0003577	PMID:17167479;PMID:17470132	PCS		15/15			C	HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0003401	PMID:17470132	PCS		0/9			P	HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0002661	PMID:17167479	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0000970	OMIM:243000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0000020	OMIM:243000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0010829	PMID:17470132	PCS		0/9			P	HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0010830	PMID:17470132	PCS		0/9			P	HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0010831	PMID:17470132	PCS		0/9			P	HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0012332	PMID:17470132	PCS		0/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0007021	PMID:17167479;PMID:17470132	PCS		15/15			P	HPO:probinson[2022-05-23];HPO:probinson[2009-02-17];HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0000007	PMID:17167479	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0000458	OMIM:243000	TAS					P	HPO:probinson[2009-02-17]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0004409	OMIM:243000	TAS					P	HPO:probinson[2009-02-17]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0000966	OMIM:243000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0040129	PMID:17470132	PCS		0/6			P	HPO:probinson[2022-05-23]
OMIM:243000	Indifference to pain, congenital, autosomal recessive		HP:0001249	PMID:17470132	PCS		0/9			P	HPO:probinson[2022-05-23]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0002982	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0005257	PMID:28812463	PCS		1/1			P	HPO:probinson[2021-09-16]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0001591	PMID:27081514	PCS	HP:0011461	1/1			P	HPO:probinson[2021-09-16]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0001790	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0010444	OMIM:166210	IEA					P	HPO:skoehler[2010-06-18]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0008873	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0000239	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0002757	OMIM:166210	TAS					P	HPO:probinson[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0001622	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0005623	PMID:28812463	PCS	HP:0011461	1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2021-09-16]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0005622	OMIM:166210	IEA					P	HPO:iea[2012-05-07]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0009826	PMID:27081514;PMID:28812463	PCS	HP:0011461	2/2			P	HPO:probinson[2021-09-16]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0000592	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0002093	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0001518	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0000926	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0006640	PMID:28812463	PCS	HP:0011461	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-16]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0001635	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0006367	PMID:27081514	PCS	HP:0011461	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-16]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0000444	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0002645	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0000883	PMID:27081514	PCS		1/1			P	HPO:probinson[2021-09-16]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0000006	PMID:6304100	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-19]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0000963	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0002644	OMIM:166210	IEA					P	HPO:iea[2009-02-17]
OMIM:166210	Osteogenesis imperfecta, type II		HP:0005855	PMID:27081514;PMID:28812463	PCS	HP:0011461	2/2			P	HPO:probinson[2021-09-16];HPO:probinson[2009-02-17];HPO:probinson[2021-09-16]
OMIM:215520	Ciliary dyskinesia due to transposition of ciliary microtubules		HP:0005425	OMIM:215520	TAS					P	HPO:probinson[2013-04-07]
OMIM:215520	Ciliary dyskinesia due to transposition of ciliary microtubules		HP:0012265	OMIM:215520	TAS					P	HPO:probinson[2013-04-07]
OMIM:215520	Ciliary dyskinesia due to transposition of ciliary microtubules		HP:0000007	OMIM:215520	IEA					I	HPO:iea[2009-02-17]
OMIM:215520	Ciliary dyskinesia due to transposition of ciliary microtubules		HP:0005938	OMIM:215520	TAS					P	HPO:probinson[2013-04-07]
OMIM:604802	Huntington disease-like 3		HP:0002300	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0006913	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0001332	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0002167	OMIM:604802	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0001250	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0001371	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0002340	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0000020	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0001251	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0002072	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0002062	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0002071	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0002607	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0000007	OMIM:604802	IEA					I	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0007256	OMIM:604802	TAS					P	HPO:skoehler[2015-01-04]
OMIM:604802	Huntington disease-like 3		HP:0002317	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0001257	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:604802	Huntington disease-like 3		HP:0001268	OMIM:604802	IEA					P	HPO:iea[2009-02-17]
OMIM:174600	Polydactyly, preaxial III		HP:0001199	OMIM:174600	IEA					P	HPO:iea[2009-02-17]
OMIM:174600	Polydactyly, preaxial III		HP:0100258	OMIM:174600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:174600	Polydactyly, preaxial III		HP:0000006	OMIM:174600	IEA					I	HPO:iea[2009-02-17]
OMIM:187950	Thrombocythemia 1		HP:0001894	PMID:10583217;PMID:3953624	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-11];HPO:probinson[2020-09-11]
OMIM:187950	Thrombocythemia 1		HP:0008320	PMID:3953624	PCS		3/3			P	HPO:probinson[2020-09-11]
OMIM:187950	Thrombocythemia 1		HP:0008148	PMID:3953624	PCS		3/3			P	HPO:probinson[2020-09-11]
OMIM:187950	Thrombocythemia 1		HP:0000006	PMID:10583217	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-11]
OMIM:187950	Thrombocythemia 1		HP:0001744	PMID:3953624	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-11]
OMIM:187950	Thrombocythemia 1		HP:0004866	PMID:3953624	PCS		3/3			P	HPO:probinson[2020-09-11]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0003552	OMIM:255110	IEA					P	HPO:iea[2009-02-17]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0003201	PMID:15642848	PCS		5/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0000083	PMID:15642848	PCS		5/28			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0011463	PMID:15642848	PCS					C	HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0003394	OMIM:255110	IEA					P	HPO:iea[2009-02-17]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0011462	PMID:15642848	PCS					C	HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0002913	PMID:15642848	PCS		22/28		HP:0025377	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0000007	PMID:15642848	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0001324	PMID:15642848	PCS		17/28		HP:0025377	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0000006	PMID:15642848	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-14]
OMIM:255110	Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced		HP:0003326	PMID:15642848	PCS		27/28		HP:0025377	P	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001276	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0000341	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0003577	PMID:31271740	PCS		2/2			C	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002169	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0004322	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001250	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001252	PMID:31271740	PCS		2/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0003593	PMID:34918187	PCS		2/2			C	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0012704	PMID:34918187	PCS		2/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0100704	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002878	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001601	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001623	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001249	PMID:31271740	PCS		1/1			P	HPO:probinson[2022-06-01];HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0003348	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001347	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002179	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002510	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002015	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002059	PMID:34918187;PMID:31271740	PCS		3/4			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001561	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0006956	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0000054	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0000252	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002133	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002376	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0003487	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0000293	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0011968	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002373	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002451	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002151	PMID:31271740	PCS		2/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001263	PMID:34918187;PMID:31271740	PCS		4/4			P	HPO:probinson[2022-06-01];HPO:probinson[2022-06-01];HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0002171	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0100021	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0033454	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0003819	PMID:34918187	PCS		2/2			C	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001518	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0000407	PMID:31271740	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0011451	PMID:31271740	PCS		2/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0000007	PMID:31271740	PCS					I	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001257	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0000028	PMID:34918187;PMID:31271740	PCS		2/4			P	HPO:probinson[2022-06-01]
OMIM:619847	Neurodegeneration, childhood-onset, with progressive microcephaly		HP:0001336	PMID:34918187	PCS		1/2			P	HPO:probinson[2022-06-01]
OMIM:310470	Neuropathy, hereditary sensory, X-linked		HP:0001417	OMIM:310470	TAS					I	HPO:probinson[2009-02-17]
OMIM:310470	Neuropathy, hereditary sensory, X-linked		HP:0003380	OMIM:310470	TAS					P	HPO:probinson[2013-04-07]
OMIM:310470	Neuropathy, hereditary sensory, X-linked		HP:0000763	OMIM:310470	TAS					P	HPO:probinson[2013-03-20]
OMIM:271930	Striatonigral degeneration, infantile		HP:0002015	PMID:16786527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0001266	PMID:16786527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0002376	PMID:16786527	PCS					P	HPO:skoehler[2014-04-04];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0001332	PMID:16786527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0003593	PMID:16786527	PCS					C	HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0007281	OMIM:271930	IEA					P	HPO:iea[2009-02-17]
OMIM:271930	Striatonigral degeneration, infantile		HP:0001508	PMID:16786527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0011463	PMID:16786527	PCS					C	HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0012043	PMID:16786527	PCS					P	HPO:skoehler[2013-05-31];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0000007	PMID:16786527	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0000648	PMID:16786527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0001257	PMID:16786527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:271930	Striatonigral degeneration, infantile		HP:0001249	PMID:16786527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0003477	PMID:37467750	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000286	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000582	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0004322	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001250	PMID:37467750	PCS		6/14			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001272	PMID:37467750	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001251	PMID:37467750	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0002020	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0003593	PMID:37467750	PCS		2/2			C	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0012389	PMID:37467750	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001508	PMID:37369308;PMID:37467750	PCS		3/15			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000319	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000316	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0002119	PMID:37467750	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000219	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000278	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001347	PMID:37467750	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0003623	PMID:37369308	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0008936	PMID:37467750	PCS		7/14			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000252	PMID:37369308;PMID:37467750	PCS		7/15			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000431	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0011968	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001263	PMID:37369308;PMID:37467750	PCS		15/15			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0012817	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0045025	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0034295	PMID:37467750	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001518	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0001999	PMID:37369308;PMID:37467750	PCS		9/15			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000369	PMID:37369308	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620988	Intellectual developmental disorder, autosomal dominant 75		HP:0000006	PMID:37467750	PCS					I	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:182800	Spastic paraplegia with associated extrapyramidal signs		HP:0002071	OMIM:182800	IEA					P	HPO:iea[2009-02-17]
OMIM:182800	Spastic paraplegia with associated extrapyramidal signs		HP:0001258	OMIM:182800	IEA					P	HPO:iea[2009-02-17]
OMIM:182800	Spastic paraplegia with associated extrapyramidal signs		HP:0000006	OMIM:182800	IEA					I	HPO:iea[2009-02-17]
OMIM:610687	Nemaline myopathy 7		HP:0003577	PMID:17160903	PCS		2/2			C	HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0003236	PMID:22560515	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7		HP:0001252	PMID:17160903	PCS	HP:0003577	2/2			P	HPO:probinson[2013-01-09];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0001252	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0012548	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0003690	PMID:22560515	PCS		2/2			P	HP:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0010300	PMID:22560515	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0001270	PMID:22560515	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7		HP:0003391	PMID:22560515	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0030319	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0100297	PMID:22560515	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0010546	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7		HP:0011463	PMID:22560515	PCS		2/2			C	HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0007340	PMID:22560515	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0002816	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0002938	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0002515	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7		HP:0000218	PMID:22560515	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0003803	PMID:22560515	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7		HP:0002359	PMID:17160903	PCS		2/2			P	HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7		HP:0003789	PMID:17160903	PCS		2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7		HP:0001324	PMID:17160903	PCS		2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0003547	PMID:22560515	PCS		2/2			P	HP:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0001763	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0020203	PMID:22560515	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0001623	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17];HPO:probinson[2024-06-12]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0002751	PMID:22560515	PCS		1/2			P	HP:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0003687	PMID:22560515	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0031936	PMID:22560515	PCS		2/2			P	HP:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7		HP:0001288	PMID:22560515	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0003484	PMID:22560515	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7		HP:0001284	PMID:22560515	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7		HP:0002194	PMID:17160903;PMID:22560515	PCS		4/4			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-17];HP:probinson[2022-03-17];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0034671	PMID:22560515	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7		HP:0000007	PMID:17160903	PCS					I	HPO:probinson[2013-04-01]
OMIM:610687	Nemaline myopathy 7		HP:0002747	PMID:22560515	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7		HP:0003798	PMID:17160903;PMID:22560515	PCS		3/4			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-17];ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7		HP:0003677	PMID:17160903	PCS					C	HPO:skoehler[2013-10-06];HPO:probinson[2022-03-17]
OMIM:610687	Nemaline myopathy 7, autosomal recessive		HP:0003557	PMID:22560515	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-12]
OMIM:610687	Nemaline myopathy 7		HP:0000467	PMID:22560515	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-03-17]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0007490	OMIM:601952	IEA					P	HPO:iea[2009-02-17]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0001036	OMIM:601952	IEA					P	HPO:iea[2009-02-17]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0001795	OMIM:601952	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2012-03-03]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0008064	OMIM:601952	PCS					P	HPO:probinson[2009-02-17]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0009775	OMIM:601952	IEA					P	HPO:iea[2009-02-17]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0000007	PMID:20226437	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0007465	OMIM:601952	IEA					P	HPO:iea[2009-02-17]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0008404	OMIM:601952	PCS					P	HPO:probinson[2012-03-03]
OMIM:601952	Keratosis linearis with ichthyosis congenita and sclerosing keratoderma		HP:0007479	OMIM:601952	TAS					P	HPO:skoehler[2012-10-17]
OMIM:620744	Spermatogenic failure 90		HP:0030346	PMID:35534203	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620744	Spermatogenic failure 90		HP:0030345	PMID:35534203	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620744	Spermatogenic failure 90		HP:0034011	PMID:35534203	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620744	Spermatogenic failure 90		HP:0003251	PMID:35534203	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620744	Spermatogenic failure 90		HP:0011462	PMID:35534203	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620744	Spermatogenic failure 90		HP:0000007	PMID:35534203	PCS					I	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:620744	Spermatogenic failure 90		HP:0000798	PMID:35534203	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:235800	Histidinemia		HP:0010906	PMID:15806399	PCS		50/50			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:235800	Histidinemia		HP:0002927	OMIM:235800	PCS					P	HPO:iea[2010-12-08]
OMIM:235800	Histidinemia		HP:0000007	PMID:15806399	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:235800	Histidinemia		HP:6000621	PMID:2992472	PCS					P	HPO:probinson[2024-04-03]
OMIM:235800	Histidinemia		HP:0000006	OMIM:235800	TAS					I	HPO:skoehler[2015-12-30]
OMIM:235800	Histidinemia		HP:0001249	PMID:8669938	IEA		0/104			P	HPO:probinson[2022-05-23]
OMIM:302060	Barth syndrome		HP:0004840	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0002286	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0003593	PMID:34355125	PCS		1/1			C	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001270	PMID:34355125	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0011675	OMIM:302060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:302060	Barth syndrome		HP:0003391	PMID:10484795	PCS		1/5			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:6000517	PMID:34382226	PCS					P	HPO:probinson[2024-04-03]
OMIM:302060	Barth syndrome		HP:0001508	PMID:10484795	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001706	OMIM:302060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:302060	Barth syndrome		HP:0002837	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0000337	PMID:34355125	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0004913	OMIM:302060	IEA					P	HPO:iea[2009-02-17]
OMIM:302060	Barth syndrome		HP:0000311	PMID:34355125	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0003546	PMID:34355125	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001644	PMID:10484795	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0002058	PMID:10484795	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001762	OMIM:302060	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:302060	Barth syndrome		HP:0001288	OMIM:302060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:302060	Barth syndrome		HP:0000293	PMID:34355125	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0000490	PMID:34355125	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001263	PMID:10484795	PCS		1/5			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0012378	PMID:34355125	PCS		1/1			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0033755	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0005180	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0040289	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001419	PMID:8630491	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001639	PMID:34355125	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0000348	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001635	OMIM:302060	IEA					P	HPO:iea[2009-02-17]
OMIM:302060	Barth syndrome		HP:0008322	OMIM:302060	IEA					P	HPO:iea[2009-02-17]
OMIM:302060	Barth syndrome		HP:0000307	PMID:34355125	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001913	OMIM:302060	IEA					P	HPO:iea[2009-02-17]
OMIM:302060	Barth syndrome		HP:0003756	PMID:10484795	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0000400	PMID:34355125	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0001510	PMID:34355125	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0000303	OMIM:302060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:302060	Barth syndrome		HP:0005437	OMIM:302060	IEA					P	HPO:iea[2009-02-17]
OMIM:302060	Barth syndrome		HP:0001875	PMID:10484795	PCS		5/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-14]
OMIM:302060	Barth syndrome		HP:0003535	PMID:10484795	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-05-14]
OMIM:266280	RAPADILINO syndrome		HP:0002014	OMIM:266280;PMID:12952869	PCS		22/24			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0000175	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0000365	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0000276	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0000331	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0004322	PMID:12952869	PCS		13/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0011968	PMID:12952869	PCS		12/14			P	HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0000581	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0001373	PMID:12952869	PCS		8/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0005198	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0001070	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0045025	OMIM:266280	IEA					P	HPO:skoehler[2018-10-08]
OMIM:266280	RAPADILINO syndrome		HP:0045075	PMID:12952869	PCS		0/13			P	HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0002209	PMID:12952869	PCS		0/14			P	HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0000007	PMID:12952869	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0002705	OMIM:266280	TAS					P	HPO:skoehler[2015-12-30]
OMIM:266280	RAPADILINO syndrome		HP:0000417	OMIM:266280	IEA					P	HPO:skoehler[2010-06-20]
OMIM:266280	RAPADILINO syndrome		HP:0006498	PMID:12952869	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0009777	PMID:12952869	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0000218	OMIM:266280	IEA					P	HPO:iea[2009-02-17]
OMIM:266280	RAPADILINO syndrome		HP:0000653	PMID:12952869	PCS		0/13			P	HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0006501	PMID:12952869	PCS		14/14			P	HPO:probinson[2009-02-17];HPO:probinson[2023-05-21]
OMIM:266280	RAPADILINO syndrome		HP:0001029	PMID:12952869	PCS		0/14			P	HPO:probinson[2023-05-21]
OMIM:620022	Stickler syndrome, type VI		HP:0000494	PMID:24273071	PCS		2/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0000483	PMID:24273071	PCS		3/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0011800	PMID:24273071	PCS		2/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0011003	PMID:24273071	PCS		2/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0005280	PMID:24273071	PCS		2/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0008081	PMID:24273071	PCS		3/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0031624	PMID:24273071	PCS		1/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0034372	PMID:24273071	PCS		3/3			P	HPO:probinson[2022-10-07]
OMIM:620022	Stickler syndrome, type VI		HP:0000407	PMID:24273071	PCS		3/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0000508	PMID:24273071	PCS		1/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0000007	PMID:24273071	PCS					I	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0001763	PMID:24273071	PCS		3/3			P	HPO:probinson[2022-09-01]
OMIM:620022	Stickler syndrome, type VI		HP:0001249	PMID:24273071	PCS		3/3			P	HPO:probinson[2022-09-01]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0003621	OMIM:608631	IEA					C	HPO:iea[2009-02-17]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0000717	OMIM:608631	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0000728	OMIM:608631	IEA					P	HPO:iea[2009-02-17]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0000723	OMIM:608631	TAS					P	HPO:skoehler[2013-06-04]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0000733	OMIM:608631	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0001426	OMIM:608631	IEA					I	HPO:iea[2009-02-17]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0000758	OMIM:608631	IEA					P	HPO:iea[2009-02-17]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0003745	OMIM:608631	IEA					I	HPO:iea[2009-02-17]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0000721	OMIM:608631	IEA					P	HPO:iea[2009-02-17]
OMIM:608631	Asperger syndrome, susceptibility to, 2		HP:0000732	OMIM:608631	IEA					P	HPO:iea[2009-02-17]
OMIM:618422	Deafness, autosomal recessive 100		HP:0003577	PMID:29590114	PCS		12/12			C	HPO:probinson[2024-03-15]
OMIM:618422	Deafness, autosomal recessive 100		HP:0001751	PMID:29590114	TAS		0/12			P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2024-03-15]
OMIM:618422	Deafness, autosomal recessive 100		HP:0000407	PMID:29590114	TAS		12/12		HP:0012828	P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2024-03-15]
OMIM:618422	Deafness, autosomal recessive 100		HP:0001098	PMID:29590114	PCS		0/4			P	HPO:probinson[2024-03-15]
OMIM:618422	Deafness, autosomal recessive 100		HP:0000007	PMID:29590114	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-15]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0002069	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0002521	PMID:28942967	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0003577	PMID:28942967	PCS		1/6			C	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0002188	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0004322	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001250	PMID:28942967	PCS		6/6		HP:0031375	P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001252	PMID:28942967	PCS		4/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0003593	PMID:28942967	PCS		3/6			C	HPO:probinson[2022-10-10];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0010841	PMID:28942967	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0032794	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0005274	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0000280	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0100704	PMID:28942967	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0011463	PMID:28942967	PCS		2/6			C	HPO:probinson[2022-10-10];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0012471	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001609	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0000316	PMID:28942967	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0000954	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0002317	PMID:28942967	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001249	PMID:28942967	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0002059	OMIM:617711	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001344	PMID:28942967	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0002133	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001762	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0002376	PMID:28942967	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0011968	OMIM:617711	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001263	PMID:28942967	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0011097	PMID:28942967	PCS		3/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0007270	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0034295	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0032792	PMID:28942967	PCS		4/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0011153	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0200134	PMID:28942967	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0001257	PMID:28942967	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0000322	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0000006	PMID:28942967	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:617711	Developmental and epileptic encephalopathy 91		HP:0000347	PMID:28942967	PCS		1/6			P	HPO:probinson[2022-10-10]
OMIM:233450	Goodpasture syndrome		HP:0045050	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0025143	PMID:362037	PCS		7/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0032979	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0030830	PMID:362037	PCS		12/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0000980	PMID:362037	PCS		18/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0000083	PMID:25462583	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0010982	OMIM:233450	TAS					I	HPO:probinson[2024-08-03]
OMIM:233450	Goodpasture syndrome		HP:0012587	PMID:362037	PCS		12/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0033030	PMID:20660402	PCS					P	HPO:probinson[2020-08-13]
OMIM:233450	Goodpasture syndrome		HP:0033174	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0001903	PMID:362037	PCS		27/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0011462	PMID:362037	PCS		22/29			C	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0100749	PMID:362037	PCS		12/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0001824	PMID:362037	PCS		4/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0001945	PMID:362037	PCS		7/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0002875	PMID:362037	PCS		25/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0000099	PMID:25462583	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0002113	PMID:362037	PCS		23/29			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0012617	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0025179	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0012735	PMID:362037	PCS		19/29			P	HPO:probinson[2021-02-17];HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0000093	PMID:362037	PCS		22/29			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0012615	PMID:362037	PCS		17/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0012378	PMID:362037	PCS		19/29			P	HPO:probinson[2021-02-17];HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0033316	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0002091	PMID:9917968	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0025392	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0025390	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0033559	PMID:25462583	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0040223	PMID:20660402	PCS		12/46			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-13]
OMIM:233450	Goodpasture syndrome		HP:0032230	PMID:20660402	PCS		22/54			P	HPO:probinson[2020-08-13]
OMIM:233450	Goodpasture syndrome		HP:0032177	PMID:30404116	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0000961	PMID:25462583	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0002789	PMID:25462583	PCS					P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0003138	PMID:362037	PCS		16/29			P	HPO:probinson[2021-02-17]
OMIM:233450	Goodpasture syndrome		HP:0002105	PMID:362037	PCS		25/29			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-17]
OMIM:305690	Genitourinary tract anomalies		HP:0000119	OMIM:305690	IEA					P	HPO:iea[2009-02-17]
OMIM:305690	Genitourinary tract anomalies		HP:0001417	OMIM:305690	IEA					I	HPO:iea[2009-02-17]
OMIM:305690	Genitourinary tract anomalies		HP:0003811	OMIM:305690	IEA					C	HPO:iea[2009-02-17]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0001132	PMID:24412933	PCS		1/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000518	PMID:24412933	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000639	PMID:24412933	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000480	PMID:24412933	PCS	HP:0003577	3/3			P	HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0025586	PMID:24412933	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0007663	PMID:24412933	PCS		3/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000007	PMID:24412933	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000612	PMID:24412933	PCS	HP:0003577	2/3			P	HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000565	PMID:24412933	PCS		2/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000577	PMID:24412933	PCS		1/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-08-10]
OMIM:216820	Coloboma, ocular, autosomal recessive		HP:0000588	PMID:24412933	PCS		3/3			P	HPO:probinson[2020-08-10]
OMIM:132090	Epilepsy, benign occipital		HP:0002353	OMIM:132090	TAS					P	HPO:skoehler[2009-02-17]
OMIM:132090	Epilepsy, benign occipital		HP:0001250	OMIM:132090	TAS					P	HPO:skoehler[2009-02-17]
OMIM:132090	Epilepsy, benign occipital		HP:0000006	OMIM:132090	TAS					I	HPO:skoehler[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000483	PMID:22940089	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000365	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001773	OMIM:209900	TAS					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000486	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001251	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0002141	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0012743	PMID:31997113	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000518	PMID:22940089;PMID:18669544	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000639	OMIM:209900;PMID:22940089	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0012393	PMID:26762677	PCS					P	HP:probinson[2019-02-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0011463	PMID:18669544	PCS		4/9			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001328	PMID:26762677	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-02-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000678	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0009466	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001769	OMIM:209900	TAS					P	HPO:iea[2013-04-08]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0008734	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000510	PMID:31997113;PMID:34526762;PMID:34262361	PCS		24/24			P	HPO:iea[2009-02-17];HP:probinson[2019-02-03];HPO:probinson[2021-10-03];HPO:probinson[2021-10-03];HPO:probinson[2022-06-09]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0007843	PMID:31997113;PMID:34262361	PCS		4/4			P	HPO:probinson[2022-06-09];HPO:probinson[2024-04-19];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001007	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001249	PMID:34526762;PMID:22940089;PMID:18669544	PCS		26/33			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000556	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0002311	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000054	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0009806	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001263	PMID:31997113;PMID:22940089	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0010750	PMID:22940089	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0100259	PMID:34526762;PMID:22940089;PMID:18669544	PCS		21/33			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000007	PMID:9039982	PCS					I	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0002705	OMIM:209900	TAS					P	HPO:skoehler[2015-12-30]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0007994	PMID:34262361	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0007737	PMID:34262361	PCS		3/3			P	HPO:probinson[2022-06-09];HPO:probinson[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0003577	PMID:22940089;PMID:34262361	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2022-06-09]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000662	PMID:22940089;PMID:34262361;PMID:18669544	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2022-06-09]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0002167	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001156	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0030631	PMID:31997113	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001395	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000819	PMID:34526762	PCS		7/22			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001829	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000855	PMID:31997113	PCS		1/1			P	HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0007663	PMID:31997113;PMID:22940089;PMID:34262361;PMID:18669544	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2021-10-03];HPO:probinson[2022-06-09]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000218	PMID:31997113	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000135	PMID:26762677	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-02-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000256	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000137	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000077	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0003621	PMID:18669544	PCS		5/9			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000750	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0002650	PMID:18669544	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001162	PMID:31997113	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0002099	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0002251	OMIM:209900	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001080	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000508	PMID:22940089	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000822	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000668	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001712	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000546	PMID:31997113	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001956	PMID:34526762	PCS		18/22			P	HPO:probinson[2021-10-03]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001830	PMID:34262361	PCS		1/1			P	HPO:probinson[2022-06-09]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001159	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000501	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000545	PMID:22940089;PMID:18669544	PCS		6/13			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0001513	PMID:22940089;PMID:18669544	PCS		11/12			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000786	PMID:18669544	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:209900	Bardet-Biedl syndrome 1		HP:0000148	OMIM:209900	IEA					P	HPO:iea[2009-02-17]
OMIM:613211	Amelogenesis imperfecta, hypomaturation type, iia3		HP:0011085	OMIM:613211	TAS					P	HPO:probinson[2013-02-21]
OMIM:613211	Amelogenesis imperfecta, hypomaturation type, iia3		HP:0000705	OMIM:613211	TAS					P	HPO:probinson[2013-02-21]
OMIM:613211	Amelogenesis imperfecta, hypomaturation type, iia3		HP:0006285	OMIM:613211	TAS					P	HPO:probinson[2013-02-21]
OMIM:613211	Amelogenesis imperfecta, hypomaturation type, iia3		HP:0000007	OMIM:613211	TAS					I	HPO:probinson[2013-01-09]
OMIM:620817	MHC class II deficiency 4		HP:0002850	PMID:22390233;PMID:37584719	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0005401	PMID:22390233	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0004385	PMID:37584719	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0001252	PMID:37584719	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0001263	PMID:37584719	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0002240	PMID:22390233;PMID:37584719	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0001251	PMID:37584719	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0003593	PMID:22390233;PMID:37584719	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0012444	PMID:37584719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0032218	PMID:22390233;PMID:37584719	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0001508	PMID:37584719	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0007340	PMID:37584719	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0033222	PMID:37584719	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0000403	PMID:37584719	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0000007	PMID:37584719	PCS					I	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0008897	PMID:22390233	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0006532	PMID:37584719	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0002720	PMID:22390233;PMID:37584719	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0001744	PMID:22390233	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0003347	PMID:22390233	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0004315	PMID:22390233;PMID:37584719	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0001875	PMID:37584719	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:620817	MHC class II deficiency 4		HP:0003623	PMID:37584719	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-10-25]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0003510	OMIM:309900	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000684	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000365	PMID:35144014	PCS		22/84			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0004322	PMID:35144014;OMIM:309900;PMID:35282545	PCS		82/210			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-04];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001250	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001371	PMID:35144014	PCS		74/109			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002341	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0003593	PMID:35144014	PCS		13/79			C	HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002180	PMID:35144014	PCS		44/136			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001171	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000280	PMID:35144014;PMID:35282545	PCS		137/142			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0011463	PMID:35144014	PCS		63/79			C	HPO:probinson[2022-04-04];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001609	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0011462	PMID:35282545	PCS		1/1			C	HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000998	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000238	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000158	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0003502	OMIM:309900	TAS					P	HPO:skoehler[2012-11-26]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0007703	OMIM:309900	TAS					P	HPO:probinson[2012-07-16]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002870	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001419	OMIM:309900	IEA					I	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001537	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000403	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001654	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002786	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000687	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0030799	OMIM:309900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0004389	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000023	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002240	PMID:35282545	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0006532	PMID:35144014	PCS		7/142			P	HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000256	OMIM:309900;PMID:35282545	PCS		115/131			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000179	PMID:35282545	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002159	OMIM:309900	TAS					P	HPO:skoehler[2012-11-26]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001744	PMID:35282545	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0006536	PMID:35144014	PCS		10/142			P	HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002014	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0003621	OMIM:309900	TAS		3/79			C	HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0003541	PMID:35282545	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001761	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001085	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002099	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000470	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0034203	PMID:35282545	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0010535	PMID:35144014	PCS		13/142			P	HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0002808	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000508	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0008301	OMIM:309900	TAS					P	HPO:probinson[2012-05-28]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000943	PMID:35144014;PMID:35282545	PCS		99/126			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04];HPO:probinson[2022-04-04]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001635	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0000268	OMIM:309900	IEA					P	HPO:iea[2009-02-17]
OMIM:309900	Mucopolysaccharidosis, type II		HP:0001433	PMID:35144014	PCS		101/116			P	HPO:probinson[2022-04-04]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0002025	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0004325	PMID:27374770	PCS		9/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001177	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0002023	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000365	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000486	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0004322	PMID:27374770	PCS		10/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0004442	PMID:27374770	PCS		2/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000160	PMID:27374770	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0045074	PMID:27374770	PCS		15/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0012227	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0002979	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000253	PMID:27374770	PCS		12/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000175	PMID:27374770	PCS		2/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000054	PMID:27374770	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000453	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001382	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001263	PMID:27374770	PCS		3/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0004691	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0003083	PMID:27374770	PCS		2/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0100783	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0034271	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000407	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000007	PMID:27374770	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001217	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000047	PMID:27374770	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000520	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000369	PMID:27374770	PCS		2/15			P	HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0003577	PMID:27374770	PCS					C	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001674	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0002089	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000260	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0010709	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0030717	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0012722	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001629	PMID:27374770	PCS		3/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0100867	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0008551	PMID:27374770	PCS		13/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0006498	PMID:27374770	PCS		8/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000218	PMID:27374770	PCS		3/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001545	PMID:27374770	PCS		4/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0003422	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001363	PMID:27374770	PCS		14/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000076	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0002650	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0011706	PMID:27374770	PCS		1/15			P	HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0007099	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0008665	PMID:27374770	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001631	PMID:27374770	PCS		2/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0001510	PMID:27374770	PCS				HP:0003676	P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000028	PMID:27374770	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:617063	Meier-Gorlin syndrome 7		HP:0000545	PMID:27374770	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0001771	PMID:15148145	PCS		4/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0002421	PMID:18551513	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003697	PMID:15148145	PCS		3/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003577	PMID:18551513	PCS		1/15			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003236	PMID:15148145	PCS		4/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003676	PMID:15148145	PCS					C	HPO:skoehler[2013-05-03];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0008948	PMID:15148145	PCS		1/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003273	PMID:15148145	PCS		3/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0001252	PMID:15148145;PMID:18551513	PCS		21/21			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0002460	PMID:18551513	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003593	PMID:15148145;PMID:18551513	PCS		14/20			C	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0100295	PMID:18551513	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0001270	OMIM:613205	TAS					P	HPO:skoehler[2013-05-03]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0001508	OMIM:613205	TAS					P	HPO:skoehler[2013-05-03]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0011463	PMID:15148145;PMID:18551513	PCS		3/20			C	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0006671	PMID:18551513	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003327	PMID:18551513	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003701	PMID:18551513	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0004757	PMID:15148145	PCS		1/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003306	PMID:15148145	PCS		5/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0004756	PMID:18551513	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003700	PMID:15148145	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0032989	PMID:18551513	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003621	PMID:15148145	PCS		2/5			C	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0001883	PMID:18551513	PCS		3/15			P	HPO:skoehler[2013-06-04];HPO:probinson[2024-03-23]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0031936	PMID:18551513	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0011968	PMID:15148145	PCS		2/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003484	PMID:15148145	PCS		5/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003089	PMID:15148145	PCS		1/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0003560	PMID:18551513	PCS		15/15			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0033454	PMID:18551513	PCS		3/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0001558	PMID:18551513	PCS		3/15			P	HPO:skoehler[2013-05-03]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0002505	PMID:18551513	PCS		6/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0002747	PMID:15148145;PMID:18551513	PCS		12/20			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0000006	PMID:15148145	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0034391	PMID:15148145	PCS		4/5			P	HPO:probinson[2023-02-17]
OMIM:613205	LMNA-related congenital muscular dystrophy		HP:0000467	PMID:18551513	PCS		12/15			P	HPO:skoehler[2013-05-03]
OMIM:615674	Dowling-Degos disease 3		HP:0007441	PMID:16575392	TAS		3/11			P	HPO:lccarmody[2019-01-29];HPO:probinson[2024-03-15]
OMIM:615674	Dowling-Degos disease 3		HP:0010610	PMID:16575392	TAS		0/11			P	HPO:lccarmody[2019-01-29];HPO:probinson[2024-03-15]
OMIM:615674	Dowling-Degos disease 3		HP:0000006	PMID:16575392	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2024-03-15]
OMIM:615674	Dowling-Degos disease 3		HP:0007427	PMID:16575392	PCS		11/11			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:615112	Urofacial syndrome 2		HP:0000076	PMID:23313374	PCS		4/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000010	PMID:23313374	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000021	PMID:23313374	PCS		1/5			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0003621	PMID:23313374	PCS		3/5			C	HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000012	PMID:23313374	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000083	PMID:23313374	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000273	PMID:23313374	PCS		3/9			P	HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0003593	PMID:23313374	PCS		1/5			C	HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0005340	PMID:23313374	PCS		1/4			P	HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0032465	PMID:23313374	PCS		1/4			P	HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0011463	PMID:23313374	PCS		1/5			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000805	PMID:23313374	PCS		2/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000007	PMID:23313374	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0002019	PMID:23313374	PCS		3/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-08]
OMIM:615112	Urofacial syndrome 2		HP:0000126	PMID:23313374	PCS		1/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-08]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001650	OMIM:613563	TAS					P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000286	PMID:20543203	PCS		2/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0004322	OMIM:613563	TAS		HP:0040283			P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001252	OMIM:613563	TAS					P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0003593	PMID:20543203	PCS		3/3			C	HPO:probinson[2023-03-27];HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000957	PMID:20543203	PCS		1/3			P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0012471	PMID:20543203	PCS		2/3			P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001647	OMIM:613563	TAS					P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000316	PMID:20543203	PCS		2/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0008897	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001004	OMIM:613563	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000278	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000358	PMID:20543203	PCS		3/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0002553	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000494	OMIM:613563	TAS					P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000252	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001382	OMIM:613563	TAS		20/20			P	HPO:probinson[2013-08-11];HPO:skoehler[2015-11-15]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0002033	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001263	PMID:20543203	PCS		1/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0010310	OMIM:613563	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000767	PMID:20543203	PCS		1/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000400	OMIM:613563	TAS					P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001653	OMIM:613563	TAS					P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000006	PMID:20619386	PCS					I	HPO:probinson[2013-08-11];HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000369	OMIM:613563	TAS					P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000325	PMID:20543203	PCS		1/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000343	OMIM:613563	TAS					P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000463	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0002002	PMID:20543203	PCS		2/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0002162	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0012209	PMID:20543203	PCS		3/3			P	HPO:probinson[2013-08-11];HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0008070	PMID:20543203	PCS		1/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0006094	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001508	PMID:20543203	PCS		2/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000337	PMID:20543203	PCS		2/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000736	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0006610	OMIM:613563	TAS					P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001744	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000396	PMID:20543203	PCS		1/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0002213	PMID:20543203	PCS		1/3			P	HPO:skoehler[2017-07-13]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001561	OMIM:613563	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000750	PMID:20543203	PCS		1/3			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000470	PMID:20543203	PCS		1/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0005280	OMIM:613563	TAS					P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000508	PMID:20543203	PCS		1/3			P	HPO:probinson[2013-08-11]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0002967	OMIM:613563	TAS					P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0002007	OMIM:613563	TAS					P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0001433	PMID:20543203	PCS		2/3			P	HPO:probinson[2023-03-27]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000465	OMIM:613563	TAS					P	HPO:skoehler[2015-08-05]
OMIM:613563	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia		HP:0000028	OMIM:613563	TAS					P	HPO:skoehler[2015-08-05]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0002301	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0002013	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0002077	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0000613	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0002083	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0002183	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0001269	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0002018	OMIM:607516	IEA					P	HPO:iea[2009-02-17]
OMIM:607516	Migraine with or without aura, susceptibility to, 6		HP:0000006	OMIM:607516	IEA					I	HPO:iea[2009-02-17]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0000494	PMID:31746383	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-05]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0002650	OMIM:618436	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0001762	OMIM:618436	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0004322	OMIM:618436	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0000160	PMID:31746383	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0001181	PMID:31746383	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0010557	OMIM:618436	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0012385	PMID:31746383	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-05]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0009487	PMID:31746383	PCS		3/3			P	HPO:probinson[2022-11-05]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0000508	OMIM:618436	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0001822	OMIM:618436	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0000006	PMID:16642020	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-05]
OMIM:618436	Arthrogryposis, distal, type 2B3		HP:0000325	OMIM:618436	IEA					P	HPO:skoehler[2019-09-07]
OMIM:184450	Stuttering, familial persistent, 1		HP:0025268	PMID:26544806	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-31]
OMIM:184450	Stuttering, familial persistent, 1		HP:0011463	PMID:26544806	PCS					C	HPO:probinson[2023-01-31]
OMIM:184450	Stuttering, familial persistent, 1		HP:0000006	PMID:26544806	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-01-31]
OMIM:181500	Schizophrenia		HP:0002353	OMIM:181500	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:181500	Schizophrenia		HP:0100753	OMIM:181500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181500	Schizophrenia		HP:0000738	OMIM:181500	IEA					P	HPO:iea[2009-02-17]
OMIM:181500	Schizophrenia		HP:0007086	OMIM:181500	IEA					P	HPO:iea[2009-02-17]
OMIM:181500	Schizophrenia		HP:0410291	PMID:7669819	PCS					P	HPO:nvasilevsky[2019-02-25]
OMIM:181500	Schizophrenia		HP:0000746	OMIM:181500	IEA					P	HPO:iea[2009-02-17]
OMIM:181500	Schizophrenia		HP:0000006	OMIM:181500	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614224	Retinal arterial macroaneurysm with supravalvular pulmonic stenosis		HP:0012231	OMIM:614224	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614224	Retinal arterial macroaneurysm with supravalvular pulmonic stenosis		HP:0025355	PMID:21835307	PCS		22/22			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:614224	Retinal arterial macroaneurysm with supravalvular pulmonic stenosis		HP:0000007	PMID:21835307	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:614224	Retinal arterial macroaneurysm with supravalvular pulmonic stenosis		HP:0001642	PMID:21835307	PCS		13/13			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-11-08]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0001770	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0000175	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0007925	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0000079	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0000078	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0000161	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0000407	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0001839	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0004691	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0010554	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:46	Split hand/foot malformation 1 (SHFM1)		HP:0001171	DECIPHER:46	IEA					P	HPO:skoehler[2013-05-29]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0020181	PMID:23570799	PCS		25/25			P	HPO:probinson[2022-05-04]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0010972	OMIM:105600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0025435	PMID:23570799	PCS		25/25			P	HPO:probinson[2022-05-04]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0012543	OMIM:105600	TAS					P	HPO:probinson[2014-01-01]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0001972	OMIM:105600	TAS					P	HPO:probinson[2012-08-05]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0000006	PMID:23570799	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-04]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0000952	OMIM:105600	IEA					P	HPO:iea[2009-02-17]
OMIM:105600	Anemia, dyserythropoietic congenital, type III		HP:0004810	OMIM:105600	IEA					P	HPO:iea[2009-02-17]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002069	PMID:37183190;PMID:27066544;PMID:25045150	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000286	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002465	OMIM:610042	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0010804	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		2/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000365	PMID:35911904;PMID:21827697;PMID:19302947	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002463	OMIM:610042	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000486	PMID:34778490;PMID:25045150	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001332	PMID:23074684;PMID:37183190	PCS		0/8			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002384	PMID:26843181;PMID:27439707;PMID:37183190;PMID:16571880	PCS		18/18			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001250	PMID:35911904;PMID:21827697;PMID:27439707;PMID:17646849;PMID:37183190;PMID:19302947;PMID:25045150	PCS		16/18			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0010808	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001252	PMID:34778490;PMID:23074684;PMID:30762603;PMID:27439707;PMID:37183190;PMID:33042910	PCS		16/27			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0003196	PMID:19896112;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001251	PMID:23074684;PMID:37183190	PCS		6/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-08-19];ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0003593	PMID:34778490;PMID:34737720;PMID:23074684;PMID:19896112;PMID:21827697;PMID:27439707;PMID:37183190;PMID:33042910;PMID:25045150;PMID:34641913	PCS		16/35			C	ORCID:0000-0002-0736-9199[2024-08-19];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001290	OMIM:610042	IEA					P	HPO:skoehler[2019-04-18]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000280	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:27439707;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		1/50			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:skoehler[2019-04-18];HPO:probinson[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0032752	PMID:34778490;PMID:22031302;PMID:23074684;PMID:35911904;PMID:33895390;PMID:37183190;PMID:27439707;PMID:33042910	PCS		3/34			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0045075	PMID:19896112;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0033725	PMID:34778490;PMID:26843181;PMID:19896112;PMID:35911904;PMID:30762603;PMID:33895390;PMID:27439707;PMID:37183190	PCS		4/38			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0012469	PMID:34737720;PMID:34778490;PMID:22031302;PMID:26843181;PMID:27439707	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0011463	PMID:26843181;PMID:23074684;PMID:19896112;PMID:33895390;PMID:30762603;PMID:27439707;PMID:37183190	PCS		31/38			C	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000319	PMID:19896112;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000718	PMID:23074684;PMID:26843181;PMID:35911904;PMID:33895390;PMID:21827697;PMID:27439707;PMID:37183190;PMID:16571880;PMID:33042910	PCS		14/33			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0011220	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0012471	PMID:19896112	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0011462	PMID:17646849	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000316	PMID:34778490;PMID:19896112;PMID:16571880;PMID:25045150	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000752	PMID:16571880	PCS					P	HPO:probinson[2013-03-31];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002019	PMID:26843181;PMID:19896112;PMID:30762603;PMID:33895390;PMID:27439707;PMID:27066544;PMID:34641913	PCS		5/12			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:27439707	PCS	HP:0011463	1/1			P	HPO:probinson[2013-03-31];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:21827697	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:22031302	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:27066544	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:17646849	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:25045150	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:35911904	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:19896112	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:33895390	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:26843181	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:37183190	PCS		18/18			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:34778490	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:19302947	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:30762603	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:27439707	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001249	PMID:33042910	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0009748	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		1/42			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001265	PMID:34778490;PMID:27439707;PMID:37183190;PMID:33042910;PMID:25045150	PCS		8/16			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:skoehler[2019-04-18];HPO:probinson[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000252	PMID:22031302;PMID:19896112;PMID:21827697;PMID:30762603;PMID:19302947	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001344	OMIM:610042	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002353	PMID:34778490;PMID:26843181;PMID:33895390;PMID:30762603;PMID:27439707;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910	PCS		30/37			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-08-19];ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002197	OMIM:610042	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001263	PMID:34737720;PMID:34778490;PMID:19896112;PMID:30762603;PMID:21827697;PMID:17646849;PMID:19302947;PMID:27066544;PMID:22031302;PMID:23074684;PMID:26843181;PMID:33895390;PMID:27439707;PMID:37183190;PMID:16571880;PMID:33042910;PMID:25045150;PMID:34641913	PCS		57/64			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:skoehler[2018-10-08]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000691	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		1/42			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000294	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		1/42			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0032046	PMID:34778490;PMID:26843181;PMID:19896112;PMID:33895390;PMID:30762603;PMID:27439707;PMID:37183190;PMID:16571880	PCS		2/16			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:skoehler[2019-02-22];HPO:probinson[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002194	PMID:34778490;PMID:23074684;PMID:27439707;PMID:16571880;PMID:25045150	PCS		12/13			P	HPO:probinson[2013-01-09];HPO:probinson[2023-03-04];ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0030746	PMID:34778490;PMID:26843181;PMID:19896112;PMID:35911904;PMID:33895390;PMID:30762603;PMID:27439707;PMID:37183190	PCS		9/38			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0007074	PMID:34778490;PMID:26843181;PMID:19896112;PMID:35911904;PMID:33895390;PMID:30762603;PMID:27439707;PMID:37183190	PCS		1/38			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000729	PMID:34778490;PMID:26843181;PMID:19896112;PMID:37183190;PMID:19302947;PMID:16571880;PMID:34641913	PCS		19/30			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000007	PMID:16571880	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000527	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000400	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002349	PMID:16571880	PCS		3/9			P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0007359	PMID:34778490;PMID:35911904;PMID:30762603;PMID:37183190;PMID:16571880	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000322	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001257	PMID:37183190;PMID:27439707;PMID:33042910	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-08-19];ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000687	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		2/42			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002883	PMID:23074684;PMID:19896112;PMID:21827697;PMID:37183190;PMID:27439707;PMID:16571880;PMID:25045150	PCS		8/45			P	HPO:skoehler[2019-04-18];ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000341	PMID:19896112;PMID:33895390;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000582	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		2/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002000	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0010863	PMID:23074684	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0007064	OMIM:610042	TAS					P	HPO:probinson[2013-03-31]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000817	PMID:37183190	PCS		6/14			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0032661	PMID:34778490;PMID:26843181;PMID:27439707	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000337	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000414	PMID:23074684;PMID:19896112;PMID:35911904;PMID:30762603;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		2/44			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000733	PMID:19896112;PMID:35911904;PMID:30762603;PMID:27439707;PMID:33042910;PMID:34641913	PCS		9/16			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:skoehler[2018-10-08]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0006970	PMID:34778490;PMID:26843181;PMID:19896112;PMID:30762603;PMID:27439707;PMID:19302947	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000219	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		2/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000218	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		1/42			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0009765	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		1/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000256	PMID:35911904	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0006855	PMID:34778490;PMID:26843181;PMID:35911904;PMID:33895390;PMID:30762603;PMID:27439707;PMID:37183190	PCS		5/34			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001320	PMID:26843181	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000154	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:33042910;PMID:25045150	PCS		3/43			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002059	PMID:34778490;PMID:26843181;PMID:35911904;PMID:33895390;PMID:30762603;PMID:27439707;PMID:37183190	PCS		2/36			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0003621	PMID:27066544	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000750	PMID:34778490;PMID:19896112;PMID:35911904;PMID:30762603;PMID:21827697;PMID:17646849;PMID:27066544;PMID:19302947;PMID:22031302;PMID:26843181;PMID:33895390;PMID:37183190;PMID:27439707;PMID:33042910;PMID:25045150	PCS		51/55			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002133	PMID:16571880	PCS		3/9			P	HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001321	PMID:19896112	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0010819	PMID:34778490;PMID:22031302;PMID:26843181;PMID:23074684;PMID:35911904;PMID:33895390;PMID:27439707;PMID:37183190;PMID:33042910	PCS		2/38			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0012760	OMIM:610042	TAS					P	HPO:probinson[2013-03-31]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0034295	PMID:34778490;PMID:26843181;PMID:19896112;PMID:35911904;PMID:30762603;PMID:33895390;PMID:27439707;PMID:37183190	PCS		3/38			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0100753	PMID:17646849	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0032792	PMID:34778490;PMID:22031302;PMID:23074684;PMID:26843181;PMID:35911904;PMID:33895390;PMID:37183190;PMID:27439707;PMID:33042910	PCS		11/38			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0007334	PMID:34778490;PMID:22031302;PMID:26843181;PMID:23074684;PMID:35911904;PMID:33895390;PMID:37183190;PMID:27439707;PMID:16571880;PMID:33042910	PCS		11/46			P	ORCID:0000-0002-0736-9199[2024-08-19];HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0002007	PMID:34778490;PMID:19896112;PMID:16571880;PMID:25045150	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000664	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		2/42			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0007018	PMID:16571880	PCS		8/9			P	HPO:probinson[2023-03-04]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0000303	PMID:23074684;PMID:19896112;PMID:35911904;PMID:21827697;PMID:37183190;PMID:19302947;PMID:16571880;PMID:25045150	PCS		1/42			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001513	PMID:33895390	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-19]
OMIM:610042	Pitt-Hopkins like syndrome 1		HP:0001315	OMIM:610042	TAS					P	HPO:probinson[2013-03-31]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0025114	OMIM:148700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0001806	PMID:15897387	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0025092	PMID:20082890	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0000975	PMID:19558595	TAS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0025080	PMID:15897387	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0011367	PMID:15897387	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0007501	PMID:17194569;PMID:19558595	PCS		15/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-08];HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0008404	PMID:15897387	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0000972	PMID:17194569;PMID:19558595	PCS		15/15			P	HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0007446	PMID:19558595	PCS		4/4			P	HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0000982	PMID:15897387	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2021-07-08]
OMIM:148700	Keratosis palmoplantaris striata I		HP:0000006	PMID:17194569	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-08]
OMIM:600251	Facial clefting, oblique, 1		HP:0006191	OMIM:600251	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600251	Facial clefting, oblique, 1		HP:0000175	PMID:21703590	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-11]
OMIM:600251	Facial clefting, oblique, 1		HP:0003577	PMID:21703590	PCS		1/1			C	HPO:probinson[2022-10-11]
OMIM:600251	Facial clefting, oblique, 1		HP:0000568	PMID:21703590	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:600251	Facial clefting, oblique, 1		HP:0031576	PMID:21703590	PCS		1/1			P	HPO:probinson[2022-10-11]
OMIM:600251	Facial clefting, oblique, 1		HP:0003745	OMIM:600251	TAS					I	HPO:skoehler[2015-12-30]
OMIM:600251	Facial clefting, oblique, 1		HP:0001884	PMID:21703590	PCS		1/1			P	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19];HPO:probinson[2022-10-11]
OMIM:600251	Facial clefting, oblique, 1		HP:0000589	OMIM:600251	TAS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-07-19]
OMIM:600251	Facial clefting, oblique, 1		HP:0000204	OMIM:600251	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600251	Facial clefting, oblique, 1		HP:0000006	PMID:21703590	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-11]
OMIM:616433	Immunodeficiency 40		HP:0003593	PMID:26083206	PCS		4/5			C	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0002240	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0100590	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0031402	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0031964	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0006532	PMID:26083206	PCS		2/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0001403	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0003623	PMID:26083206	PCS		1/5			C	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0005403	PMID:26083206	PCS		3/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0002113	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0006515	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0031956	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0002254	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0011947	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0005387	PMID:26083206	PCS					P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0032170	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0009098	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0033164	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0032253	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0000403	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0001954	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0000007	PMID:26083206	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0001873	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0001510	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:616433	Immunodeficiency 40		HP:0002028	PMID:26083206	PCS		1/5			P	HPO:probinson[2022-10-08]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0004446	PMID:21849667;PMID:18931342	PCS		17/17			P	HPO:probinson[2023-05-13];HPO:probinson[2023-05-13];HPO:probinson[2009-02-17];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0005502	PMID:21849667;PMID:18931342	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-13];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0003575	OMIM:185000	IEA					P	HPO:iea[2009-02-17]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0002240	OMIM:185000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0012378	PMID:21849667	PCS		1/4			P	HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0002904	PMID:21849667	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0001878	PMID:21849667;PMID:18931342	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-13];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0001923	PMID:21849667	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0005518	PMID:21849667	PCS		1/4			P	HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0001744	PMID:21849667	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0006579	PMID:21849667	PCS		1/4			P	HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0000952	PMID:21849667	PCS		3/4			P	HPO:skoehler[2015-12-30]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0000006	PMID:18931342	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0002204	PMID:21849667	PCS		2/4			P	HPO:probinson[2023-05-13];HPO:probinson[2023-05-13]
OMIM:185000	Overhydrated hereditary stomatocytosis		HP:0003623	PMID:21849667	PCS		4/4			C	HPO:probinson[2023-05-13];HPO:probinson[2023-05-13]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000341	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001374	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000486	PMID:26168268;PMID:25533962	PCS		2/15			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0002021	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001250	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0002066	PMID:26168268	PCS		5/9			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001252	PMID:26168268	PCS		10/10			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001290	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000316	OMIM:616355	TAS				HP:0012825	P	HPO:skoehler[2015-11-15]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000238	PMID:26168268;PMID:25533962	PCS		2/15			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001943	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0002119	PMID:26168268;PMID:25533962	PCS		3/15			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000256	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0005988	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001249	PMID:26168268;PMID:25533962	PCS		15/15			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000297	OMIM:616355	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000494	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001344	PMID:26168268	PCS		5/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000750	PMID:26168268	PCS		11/11			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0002650	PMID:26168268	PCS		2/11			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0031936	PMID:26168268	PCS		9/11			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000194	OMIM:616355	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000490	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001263	PMID:25533962	PCS		3/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0012378	PMID:26168268	PCS		2/11			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0031165	PMID:26168268	PCS		2/11			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000508	PMID:26168268	PCS		1/11			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0001511	PMID:26168268	PCS	HP:0003577	1/11			P	HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000006	PMID:25533962	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0000545	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616355	Houge-Janssens syndrome 1		HP:0002028	PMID:25533962	PCS		1/4			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0003026	PMID:9719382	TAS					P	HPO:probinson[2012-07-30]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0009826	OMIM:118651	TAS					P	HPO:probinson[2009-02-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0002983	OMIM:118651	TAS					P	HPO:skoehler[2012-10-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0000272	OMIM:118651	IEA					P	HPO:iea[2009-02-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0010038	OMIM:118651	TAS					P	HPO:probinson[2012-06-03]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0011800	OMIM:118651	TAS					P	HPO:skoehler[2015-11-15]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0010655	PMID:9719382	TAS					P	HPO:probinson[2009-02-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0010041	OMIM:118651	TAS					P	HPO:probinson[2012-06-03]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0010044	OMIM:118651	TAS		HP:0040283			P	HPO:probinson[2012-06-03]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0003417	OMIM:118651	TAS					P	HPO:probinson[2009-02-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0002832	OMIM:118651	TAS					P	HPO:iea[2009-02-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0005736	OMIM:118651	TAS					P	HPO:probinson[2009-02-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0000006	OMIM:118651	TAS					I	HPO:probinson[2009-02-17]
OMIM:118651	Chondrodysplasia punctata, Tibia-Metacarpal type		HP:0000457	OMIM:118651	IEA					P	HPO:iea[2009-02-17]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0000750	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0031936	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0011924	PMID:30358850	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0011925	PMID:30358850	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0001263	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0002151	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0001290	PMID:30358850	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0011800	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0002093	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0011923	PMID:30358850	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0005280	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0001508	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0001639	PMID:30358850	PCS	HP:0030674	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0001716	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0000316	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0008322	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0000007	PMID:30358850	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0008347	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0000369	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0000358	PMID:30358850	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0003128	PMID:30358850	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618378	Combined oxidative phosphorylation deficiency 38		HP:0003348	PMID:30358850	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0010628	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001377	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000343	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000463	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001250	OMIM:272430	TAS		HP:0040283			P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000160	OMIM:272430	TAS					P	HPO:skoehler[2014-11-26]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0100729	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0008872	OMIM:272430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000975	PMID:12509788	PCS				HP:0025206	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-06]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0009466	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000218	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001763	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000278	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001249	OMIM:272430	TAS		HP:0040283			P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0002751	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0002179	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000670	OMIM:272430	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0004279	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001762	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000211	OMIM:272430	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000293	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000491	OMIM:272430	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000470	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0002094	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001182	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001181	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0005280	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0012385	OMIM:272430	TAS					P	HPO:skoehler[2013-10-22]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000007	OMIM:272430	IEA					I	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001954	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0002987	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000369	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000347	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0001611	OMIM:272430	IEA					P	HPO:iea[2009-02-17]
OMIM:272430	Crisponi/cold-induced sweating syndrome 1		HP:0000445	OMIM:272430	TAS					P	HPO:skoehler[2013-01-27]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0001265	PMID:20074522	PCS		3/7			P	HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0003596	PMID:20074522	PCS		1/8			C	HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0031506	PMID:20074522	PCS		2/2			P	HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0001284	PMID:20074522	PCS		3/7			P	HPO:probinson[2022-06-12];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0000836	PMID:20074522	PCS					P	HPO:skoehler[2013-06-23];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0033077	PMID:20074522	PCS		6/7			P	HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0011462	PMID:20074522	PCS		7/8			C	HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0031098	PMID:20074522	PCS		6/6			P	HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0002900	PMID:20074522	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0001649	PMID:20074522	PCS		7/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0001824	PMID:20074522	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0003768	PMID:20074522	PCS		8/8			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0000006	PMID:20074522	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0000853	PMID:20074522	PCS		6/8			P	HPO:skoehler[2013-06-23];HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0001337	PMID:20074522	PCS		7/8			P	HPO:probinson[2022-06-12]
OMIM:613239	Thyrotoxic periodic paralysis, susceptibility to, 2		HP:0001347	PMID:20074522	PCS		1/7			P	HPO:probinson[2022-06-12]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0001298	OMIM:616341	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0002069	OMIM:616341	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0002521	OMIM:616341	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0001344	PMID:25839329	PCS		4/4			P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0002123	PMID:25839329	PCS		2/6			P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0011968	PMID:25839329	PCS					P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0001250	PMID:25839329	PCS	HP:0003593	6/6		HP:0031375	P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0002098	PMID:25839329	PCS		3/6			P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0001263	PMID:25839329	PCS		4/4		HP:0012829	P	HPO:skoehler[2015-06-22]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0000733	PMID:25839329	PCS		4/4			P	HPO:probinson[2018-03-31]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0200134	OMIM:616341	IEA					P	HPO:skoehler[2015-12-30]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0001522	PMID:25839329	PCS		2/6			C	HPO:probinson[2018-03-31]
OMIM:616341	Epileptic encephalopathy, early infantile, 30		HP:0000006	PMID:25839329	PCS					I	HPO:skoehler[2015-12-30]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0000252	PMID:32103185	PCS		2/8			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0003577	PMID:32103185	PCS		2/8			C	HPO:probinson[2022-03-17]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0000343	PMID:32103185	PCS		1/8			P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0001321	PMID:32103185	PCS		4/8			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0002365	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0002079	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0002120	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0001263	PMID:32103185	PCS		6/6			P	HPO:probinson[2021-01-01];HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0003593	PMID:32103185	PCS		1/8			C	HPO:probinson[2022-03-17]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0032794	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0012695	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0001838	PMID:32103185	PCS		1/8			P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0011463	PMID:32103185	PCS		3/8			C	HPO:probinson[2022-03-17]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0011461	PMID:32103185	PCS		2/8			C	HPO:probinson[2022-03-17]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0002804	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0000007	PMID:32103185	PCS					I	HPO:probinson[2020-12-30];HPO:probinson[2020-12-30]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0000218	PMID:32103185	PCS		1/8			P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0007359	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0000278	PMID:32103185	PCS		2/8			P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0000369	PMID:32103185	PCS		1/8			P	HPO:probinson[2021-01-01]
OMIM:619072	Neurodevelopmental disorder with seizures and brain atrophy		HP:0009879	PMID:32103185	PCS					P	HPO:probinson[2021-01-01]
OMIM:620195	Obesity and hypopigmentation		HP:0001397	PMID:36536132	PCS	HP:0011463	1/1			P	HPO:probinson[2023-06-11]
OMIM:620195	Obesity and hypopigmentation		HP:0011463	PMID:36536132	PCS		1/1			C	HPO:probinson[2023-06-11]
OMIM:620195	Obesity and hypopigmentation		HP:0002297	PMID:36536132	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620195	Obesity and hypopigmentation		HP:0002591	PMID:36536132	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620195	Obesity and hypopigmentation		HP:0001548	PMID:36536132	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620195	Obesity and hypopigmentation		HP:0000006	PMID:36536132	PCS					I	HPO:probinson[2023-06-11]
OMIM:620195	Obesity and hypopigmentation		HP:0001513	PMID:36536132	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:620195	Obesity and hypopigmentation		HP:0000842	PMID:36536132	PCS		1/1			P	HPO:probinson[2023-06-11]
OMIM:117210	Spinocerebellar ataxia 31		HP:0007979	OMIM:117210	TAS		HP:0040282			P	HPO:probinson[2012-04-01]
OMIM:117210	Spinocerebellar ataxia 31		HP:0000639	OMIM:117210	TAS					P	HPO:probinson[2012-07-17]
OMIM:117210	Spinocerebellar ataxia 31		HP:0001272	OMIM:117210	TAS					P	HPO:probinson[2012-07-17]
OMIM:117210	Spinocerebellar ataxia 31		HP:0001260	OMIM:117210	IEA					P	HPO:iea[2009-02-17]
OMIM:117210	Spinocerebellar ataxia 31		HP:0002066	OMIM:117210	IEA					P	HPO:iea[2009-02-17]
OMIM:117210	Spinocerebellar ataxia 31		HP:0000407	OMIM:117210	TAS		HP:0040283			P	HPO:probinson[2012-04-01]
OMIM:117210	Spinocerebellar ataxia 31		HP:0003584	OMIM:117210	TAS		HP:0040282			C	HPO:probinson[2012-04-01]
OMIM:117210	Spinocerebellar ataxia 31		HP:0001251	OMIM:117210	TAS					P	HPO:probinson[2012-07-17]
OMIM:117210	Spinocerebellar ataxia 31		HP:0002070	OMIM:117210	IEA					P	HPO:iea[2009-02-17]
OMIM:117210	Spinocerebellar ataxia 31		HP:0000006	OMIM:117210	IEA					I	HPO:iea[2009-02-17]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0001276	PMID:34653363	PCS		5/15			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0002389	PMID:34653363	PCS		1/3			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0003596	PMID:34653363	PCS		1/16			C	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000486	PMID:34653363	PCS		2/14			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0004322	PMID:34653363	PCS		3/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0003394	PMID:34653363	PCS		7/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0003593	PMID:34653363	PCS		4/16			C	HPO:probinson[2022-03-18];HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0012745	PMID:34653363	PCS		6/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0001270	PMID:34653363	PCS		9/13			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0011463	PMID:34653363	PCS		1/16			C	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0011462	PMID:34653363	PCS		6/16			C	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000718	PMID:34653363	PCS		2/14			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0100702	PMID:34653363	PCS		1/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000219	PMID:34653363	PCS		8/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0100309	PMID:34653363	PCS		1/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0002758	PMID:34653363	PCS		4/15			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000256	PMID:34653363	PCS		3/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0001249	PMID:34653363	PCS		9/15			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0003623	PMID:34653363	PCS		1/16			C	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0003621	PMID:34653363	PCS		3/16			C	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000252	PMID:34653363	PCS		1/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000431	PMID:34653363	PCS		6/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000750	PMID:34653363	PCS		7/13			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000276	PMID:34653363	PCS		3/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0003186	PMID:34653363	PCS		4/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0400004	PMID:34653363	PCS		2/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0009890	PMID:34653363	PCS		9/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0001511	PMID:34653363	PCS		2/16			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0003712	PMID:34653363	PCS		4/15			P	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000006	PMID:34653363	PCS					I	HPO:probinson[2022-03-18]
OMIM:619714	Congenital disorder of glycosylation, type Iw, autosomal dominant		HP:0000303	PMID:34653363	PCS		5/16			P	HPO:probinson[2022-03-18]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0008392	OMIM:300918	TAS					P	HPO:skoehler[2014-08-24]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0007418	OMIM:300918	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0001036	OMIM:300918	TAS					P	HPO:skoehler[2014-08-24]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0025610	OMIM:300918	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0001419	OMIM:300918	TAS					I	HPO:skoehler[2015-12-30]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0025092	OMIM:300918	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0000972	OMIM:300918	TAS				HP:0012828	P	HPO:skoehler[2014-08-24]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0000982	OMIM:300918	IEA					P	HPO:skoehler[2015-01-27]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0000498	OMIM:300918	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300918	Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked		HP:0000962	OMIM:300918	TAS					P	HPO:skoehler[2014-08-24]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0002089	PMID:28264986	PCS	HP:0003577	11/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000089	OMIM:236500	IEA					P	HPO:iea[2009-02-17]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0002365	PMID:28264986	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000463	PMID:28264986	PCS					P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0001156	PMID:28264986	PCS		3/3			P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0012725	PMID:28264986	PCS	HP:0003577	7/7			P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:4000150	PMID:28264986	PCS		3/3			P	HPO:probinson[2023-01-27]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000418	PMID:28264986	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000954	PMID:28264986	PCS	HP:0003577	3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0003826	PMID:28264986	PCS		6/12			C	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000414	PMID:28264986	PCS					P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0005989	PMID:28264986	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000476	PMID:28264986	PCS	HP:0030674	3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000110	PMID:28264986	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0001562	PMID:28264986	PCS	HP:0030674	11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0001762	PMID:28264986	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000452	PMID:28264986	PCS					P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0001321	PMID:28264986	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000470	PMID:28264986	PCS					P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0045025	PMID:28264986	PCS					P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0004691	OMIM:236500	TAS					P	HPO:probinson[2009-02-17]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0012300	PMID:28264986	PCS	HP:0003577	11/11			P	HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000308	PMID:28264986	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000107	OMIM:236500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000007	PMID:28264986	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0002804	PMID:28264986	PCS		12/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0002009	PMID:28264986	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0004209	PMID:28264986	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0003811	PMID:28264986	PCS		2/12			C	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0000369	PMID:28264986	PCS	HP:0003577	3/3			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		HP:0002324	PMID:28264986	PCS	HP:0003577	12/12			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0002069	PMID:18756473	PCS		4/9			P	HPO:probinson[2024-02-17]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0003621	PMID:18756473	PCS		1/1			C	HPO:probinson[2024-02-17]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0001250	PMID:18756473	PCS		9/9			P	HPO:probinson[2024-02-17]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0002384	PMID:18756473	PCS		2/9			P	HPO:probinson[2024-02-17]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0002373	PMID:18756473	PCS		1/9			P	HPO:probinson[2024-02-17]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0002121	PMID:18756473	PCS		2/9			P	HPO:probinson[2024-02-17]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0000006	PMID:18756473	PCS					I	HPO:probinson[2024-02-17]
OMIM:612899	Epilepsy idiopathic generalized, susceptibility to, 8		HP:0001336	PMID:18756473	PCS		4/9			P	HPO:probinson[2024-02-17]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000286	PMID:21802062	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0003577	PMID:21802062	PCS		8/8			C	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000321	PMID:21802062	PCS		1/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000486	PMID:21802062	PCS		4/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0002263	PMID:21802062	PCS		7/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0001252	PMID:21802062	PCS		5/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000580	PMID:21802062	PCS		1/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0010489	PMID:21802062	PCS		4/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0032277	PMID:21802062	PCS		1/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0010049	PMID:21802062	PCS		1/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0012745	PMID:21802062	PCS		6/8			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000518	PMID:21802062	PCS		3/8			P	HPO:probinson[2022-04-23];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000316	PMID:21802062	PCS		2/7			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0003429	PMID:21802062	PCS		2/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0002714	PMID:21802062	PCS		6/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000218	PMID:21802062	PCS		2/7			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000411	PMID:21802062	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0003745	PMID:21802062	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0009921	PMID:21802062	PCS		1/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000311	PMID:21802062	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0001249	PMID:21802062	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000175	PMID:21802062	PCS		1/7			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000494	PMID:21802062	PCS		4/8			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000054	PMID:21802062	PCS		1/4			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000431	PMID:21802062	PCS		6/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0002079	PMID:21802062	PCS		3/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000430	PMID:21802062	PCS		6/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000293	PMID:21802062	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000470	PMID:21802062	PCS		4/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0012385	PMID:21802062	PCS		2/8			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000407	PMID:21802062	PCS		3/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000729	PMID:21802062	PCS		1/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0010780	PMID:21802062	PCS		1/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000508	PMID:21802062	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000348	PMID:21802062	PCS		6/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000568	PMID:21802062	PCS		2/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000647	PMID:21802062	PCS		3/8			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0001159	PMID:21802062	PCS		1/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0001510	PMID:21802062	PCS		3/7			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000322	PMID:21802062	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000006	PMID:21802062	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000028	PMID:21802062	PCS		2/4			P	HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000369	PMID:21802062	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
OMIM:614230	Chromosome 8q21.11 deletion syndrome		HP:0000347	PMID:21802062	PCS		6/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-23]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0000252	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0000463	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0010808	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0001252	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0003196	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0011800	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0001627	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0000664	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:52	9q subtelomeric deletion syndrome		HP:0001249	DECIPHER:52	IEA					P	HPO:skoehler[2013-05-29]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000175	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000252	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0001245	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0011803	OMIM:239800	TAS					P	HPO:probinson[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000160	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000086	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0001263	OMIM:239800	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0004691	OMIM:239800	TAS					P	HPO:probinson[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000925	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0008551	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000316	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000007	OMIM:239800	IEA					I	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0030680	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0001627	OMIM:239800	TAS					P	HPO:skoehler[2015-12-30]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000405	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0009237	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000455	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000204	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000413	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0000347	OMIM:239800	TAS				HP:0012825	P	HPO:probinson[2012-04-30]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0003468	OMIM:239800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:239800	Hypertelorism, microtia, facial clefting syndrome		HP:0002006	OMIM:239800	IEA					P	HPO:iea[2009-02-17]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000483	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0001250	PMID:28628100	PCS		1/4			P	HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0002020	PMID:28628100	PCS		1/4			P	HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0003593	PMID:35675825	PCS		4/4			C	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0010862	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0001270	PMID:28628100	PCS		2/3			P	HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0100034	PMID:28628100	PCS		1/3			P	HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0012471	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0007302	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000752	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0001249	PMID:35675825;PMID:28628100	PCS		8/8			P	HPO:probinson[2022-08-08];HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000750	PMID:28628100	PCS		3/3			P	HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0001344	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0001260	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0001263	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0002194	PMID:35675825	PCS		2/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0011327	PMID:28628100	PCS		1/4			P	HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000506	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000729	PMID:35675825;PMID:28628100	PCS		5/8			P	HPO:probinson[2022-08-08];HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000722	PMID:28628100	PCS		1/3			P	HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000821	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0002205	PMID:35675825	PCS		1/4			P	HPO:probinson[2022-08-08]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0007018	PMID:35675825;PMID:28628100	PCS		3/7			P	HPO:probinson[2022-08-08];HPO:probinson[2022-08-06]
OMIM:619927	Intellectual developmental disorder, autosomal dominant 67		HP:0000006	PMID:28628100	PCS					I	HPO:probinson[2022-08-06]
OMIM:274900	Thyroid hormonogenesis, genetic defect in, 5		HP:0001939	OMIM:274900	IEA					P	HPO:iea[2009-02-17]
OMIM:274900	Thyroid hormonogenesis, genetic defect in, 5		HP:0000007	OMIM:274900	IEA					I	HPO:skoehler[2010-06-19]
OMIM:274900	Thyroid hormonogenesis, genetic defect in, 5		HP:0000821	OMIM:274900	IEA					P	HPO:iea[2009-02-17]
OMIM:274900	Thyroid hormonogenesis, genetic defect in, 5		HP:0001510	OMIM:274900	IEA					P	HPO:iea[2009-02-17]
OMIM:274900	Thyroid hormonogenesis, genetic defect in, 5		HP:0000853	OMIM:274900	IEA					P	HPO:iea[2009-02-17]
OMIM:274900	Thyroid hormonogenesis, genetic defect in, 5		HP:0001249	OMIM:274900	IEA					P	HPO:iea[2009-02-17]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001265	PMID:27683825	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0003477	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0003236	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0003376	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001310	PMID:27683825	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001761	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001272	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0003693	PMID:27683825	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001260	PMID:27683825	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0002066	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0002352	OMIM:618387	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001263	PMID:27683825	PCS		1/1			P	HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001251	PMID:27683825	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0002460	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0011402	PMID:27683825	PCS		1/1			P	HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0003690	PMID:27683825	PCS	HP:0003621	1/1			P	HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0011463	PMID:27683825	PCS		1/1			C	HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0009027	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0000007	PMID:27683825	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0002936	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0003677	PMID:27683825	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001337	PMID:27683825	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-20]
OMIM:618387	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3		HP:0001765	OMIM:618387	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608194	Cone-rod dystrophy 13		HP:0001133	PMID:28456785;PMID:34722527	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0007737	PMID:34722527	PCS		7/13			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0003577	PMID:34722527	PCS		2/11			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0031605	PMID:12920066	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000662	PMID:28456785;PMID:34722527;PMID:25943428	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000540	PMID:34722527	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0003593	PMID:28456785;PMID:34722527	PCS		3/13			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0032037	PMID:34722527;PMID:25943428	PCS		4/14			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0030515	PMID:34722527;PMID:25943428	PCS		8/14			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000639	PMID:28456785;PMID:34722527;PMID:25943428	PCS		11/16			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0011463	PMID:28456785;PMID:34722527	PCS		5/13			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0032122	PMID:28456785;PMID:34722527;PMID:25943428	PCS		4/16			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000613	PMID:12920076	PCS	HP:0011463				P	HPO:probinson[2013-03-24];HPO:probinson[2020-07-23]
OMIM:608194	Cone-rod dystrophy 13		HP:0000613	PMID:25943428	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000613	PMID:34722527	PCS		3/13			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000613	PMID:12920066	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0007663	PMID:12920076	PCS	HP:0003621				P	HPO:probinson[2013-03-24];HPO:probinson[2020-07-23]
OMIM:608194	Cone-rod dystrophy 13		HP:0007663	PMID:12920066	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0007401	PMID:34722527	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0007787	PMID:34722527	PCS		6/13			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0007688	PMID:12920076	PCS					P	HPO:probinson[2013-03-24];HPO:probinson[2020-07-23]
OMIM:608194	Cone-rod dystrophy 13		HP:0007843	PMID:28456785;PMID:34722527	PCS		7/14			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000512	PMID:28456785;PMID:34722527;PMID:12920066;PMID:25943428	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0003621	PMID:12920066;PMID:34722527;PMID:25943428	PCS		7/17			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000551	PMID:12920076	PCS	HP:0011463				P	HPO:probinson[2013-03-24];HPO:probinson[2020-07-23]
OMIM:608194	Cone-rod dystrophy 13		HP:0000551	PMID:12920066	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0003581	PMID:34722527	PCS		2/11			C	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0001141	PMID:34722527;PMID:25943428	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0011505	PMID:34722527	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000529	PMID:28456785;PMID:12920066	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000608	PMID:12920066;PMID:12920076	PCS		15/15			P	HPO:probinson[2013-03-24];HPO:probinson[2020-07-23];ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000007	PMID:12920076	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-23]
OMIM:608194	Cone-rod dystrophy 13		HP:0000505	PMID:12920076	PCS					P	HPO:probinson[2013-03-24];HPO:probinson[2020-07-23]
OMIM:608194	Cone-rod dystrophy 13		HP:0000548	PMID:12920076	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-23]
OMIM:608194	Cone-rod dystrophy 13		HP:0000543	PMID:34722527	PCS		4/13			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:608194	Cone-rod dystrophy 13		HP:0000545	PMID:34722527	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-11-02]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0003477	PMID:32934225	PCS		4/4			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0002751	PMID:32934225	PCS		4/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0000750	PMID:32934225	PCS		9/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0003693	PMID:32934225	PCS		7/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0002098	PMID:32934225	PCS		1/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0001263	PMID:32934225	PCS		7/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0003593	PMID:32934225	PCS		2/9			C	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0001251	PMID:32934225	PCS		3/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0001290	PMID:32934225	PCS		4/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0011463	PMID:32934225	PCS		7/9			C	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0000007	PMID:32934225	PCS					I	HPO:probinson[2020-12-15];HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0001249	PMID:32934225	PCS		7/9			P	HPO:probinson[2020-12-15]
OMIM:619099	Intellectual developmental disorder with speech delay and axonal peripheral neuropathy		HP:0001337	PMID:32934225	PCS		2/8			P	HPO:probinson[2020-12-15]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0003202	PMID:30543681	PCS		3/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0003577	OMIM:618393	IEA					C	HPO:skoehler[2019-09-07]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0001561	PMID:30543681	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000475	PMID:30543681	PCS		1/3			P	HPO:skoehler[2019-09-07]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000431	PMID:30543681	PCS		4/4			P	HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0025676	PMID:30543681	PCS		1/5			P	HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000470	PMID:30543681	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0010963	PMID:30543681	PCS		1/5			P	HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0012385	PMID:30543681	PCS		3/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0034241	PMID:30543681	PCS		2/3			C	HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0001838	PMID:30543681	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0002808	PMID:30543681	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0034198	PMID:30543681	PCS		5/5			C	HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0002804	PMID:30543681	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000007	PMID:30543681	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0001558	PMID:30543681	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000878	PMID:30543681	PCS		2/3			P	HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000218	PMID:30543681	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0003811	PMID:30543681	PCS		1/3			C	HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000278	PMID:30543681	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000028	PMID:30543681	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000369	PMID:30543681	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000347	PMID:30543681	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:618393	Fetal akinesia deformation sequence 4		HP:0000358	PMID:30543681	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-21]
OMIM:608180	Synpolydactyly 2		HP:0001440	OMIM:608180	IEA					P	HPO:iea[2009-02-17]
OMIM:608180	Synpolydactyly 2		HP:0001770	OMIM:608180	IEA					P	HPO:iea[2009-02-17]
OMIM:608180	Synpolydactyly 2		HP:0008368	OMIM:608180	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608180	Synpolydactyly 2		HP:0010442	OMIM:608180	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608180	Synpolydactyly 2		HP:0009702	OMIM:608180	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608180	Synpolydactyly 2		HP:0009701	OMIM:608180	IEA					P	HPO:iea[2009-02-17]
OMIM:608180	Synpolydactyly 2		HP:0000006	OMIM:608180	IEA					I	HPO:iea[2009-02-17]
OMIM:179250	Radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillarydiastema		HP:0000047	OMIM:179250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:179250	Radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillarydiastema		HP:0005725	OMIM:179250	IEA					P	HPO:iea[2009-02-17]
OMIM:179250	Radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillarydiastema		HP:0000006	OMIM:179250	IEA					I	HPO:iea[2009-02-17]
OMIM:179250	Radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillarydiastema		HP:0000699	OMIM:179250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:179250	Radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillarydiastema		HP:0002984	OMIM:179250	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000121	OMIM:130650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0002884	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001052	OMIM:130650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0002240	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000280	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0032165	PMID:18342934	PCS					P	HPO:probinson[2021-10-15]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000239	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001548	OMIM:130650	TAS					P	HPO:skoehler[2010-06-20]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001305	OMIM:130650	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0006277	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001528	OMIM:130650	TAS					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000158	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001540	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0003247	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000076	OMIM:130650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001640	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000150	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0005487	OMIM:130650	TAS					P	HPO:probinson[2017-05-25]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0011800	OMIM:130650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0008186	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000803	OMIM:130650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001998	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001638	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0001539	OMIM:130650	TAS					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0008523	PMID:17223397	PCS					P	HPO:probinson[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0005616	OMIM:130650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0002667	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000520	PMID:23511928	PCS					P	HPO:probinson[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0006744	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000006	OMIM:130650	TAS					I	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000028	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000105	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000787	OMIM:130650	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130650	Beckwith-Wiedemann syndrome		HP:0000269	OMIM:130650	IEA					P	HPO:iea[2009-02-17]
OMIM:617936	Butyrylcholinesterase deficiency		HP:0000007	PMID:21637541	PCS					I	HPO:probinson[2020-08-03];HPO:probinson[2020-08-03]
OMIM:617936	Butyrylcholinesterase deficiency		HP:0002104	PMID:21637541	PCS				HP:0034195	P	HPO:probinson[2022-04-15]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0003596	PMID:34953004	PCS		1/1			C	HPO:probinson[2022-07-19]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0005312	OMIM:178600	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0005168	OMIM:178600	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0002094	OMIM:178600	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0012735	PMID:34953004	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0002092	PMID:34953004;PMID:11015450	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0011353	OMIM:178600	TAS					P	HPO:skoehler[2013-01-22]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0001708	PMID:9729004	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0011462	PMID:11015450	PCS		9/9			C	HPO:probinson[2022-07-19]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0003829	PMID:8988890	PCS					I	HPO:iea[2010-07-08]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0001977	OMIM:178600	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0000822	OMIM:178600	TAS					P	HPO:skoehler[2013-01-22]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0001009	OMIM:178600	TAS					P	HPO:skoehler[2013-01-22]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0005308	OMIM:178600	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0000006	PMID:10973254	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-19]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0001667	PMID:9729004	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0005317	PMID:9729004	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:178600	Pulmonary hypertension, primary, 1		HP:0004964	OMIM:178600	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0001265	OMIM:300717	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0002421	PMID:18274675	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0003236	PMID:18274675	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0002650	PMID:18274675	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0001371	OMIM:300717	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0001284	OMIM:300717	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0011421	PMID:18274675	PCS		1/2			C	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0034320	PMID:18274675	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0011463	PMID:18274675	PCS		2/2			C	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0002878	PMID:18274675	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0002505	PMID:18274675	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0002747	PMID:18274675	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0003701	PMID:18274675	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0001423	PMID:18274675	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0003306	PMID:18274675	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0003557	OMIM:300717	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300717	Myopathy, reducing body, X-linked, early-onset, severe		HP:0003678	PMID:18274675	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-18]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0012242	OMIM:135700	TAS					P	HPO:probinson[2013-04-02]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0007936	OMIM:135700	TAS					P	HPO:probinson[2009-02-17]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0001491	OMIM:135700	TAS					P	HPO:probinson[2009-02-17]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0012241	OMIM:135700	TAS					P	HPO:probinson[2013-04-02]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0000565	OMIM:135700	TAS					P	HPO:skoehler[2010-06-20]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0001488	OMIM:135700	TAS					P	HPO:probinson[2009-02-17]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0001477	OMIM:135700	TAS					P	HPO:probinson[2009-02-17]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0031721	OMIM:135700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0000006	PMID:14595441	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-26]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0000577	OMIM:135700	TAS					P	HPO:skoehler[2010-06-20]
OMIM:135700	Fibrosis of extraocular muscles, congenital, 1		HP:0031723	OMIM:135700	IEA					P	HPO:skoehler[2018-10-08]
DECIPHER:85	8p23.1 duplication syndrome		HP:0000750	DECIPHER:85	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:85	8p23.1 duplication syndrome		HP:0001249	DECIPHER:85	IEA					P	HPO:skoehler[2013-05-29]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0000819	PMID:9435328	PCS	HP:0003584	1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0003621	PMID:9435328	PCS		4/5			C	HPO:probinson[2022-09-03]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0000825	PMID:9435328	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0002173	PMID:9435328	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0011462	PMID:9435328	PCS		1/5			C	HPO:probinson[2022-09-03]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0000006	PMID:9435328	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0001249	OMIM:602485	IEA					P	HPO:iea[2009-02-17]
OMIM:602485	Hyperinsulinemic hypoglycemia, familial, 3		HP:0001325	OMIM:602485	IEA					P	HPO:iea[2009-02-17]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0030479	PMID:9662399	PCS					P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0000639	PMID:9662399	PCS		4/7			P	HPO:probinson[2022-09-03]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0007663	PMID:9662399	PCS		7/7			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-09-03]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0000505	PMID:9662399	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0007642	PMID:9662399	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0001417	PMID:9662399	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2022-09-03]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0007984	PMID:9662399	PCS		7/7			P	HPO:probinson[2022-09-03]
OMIM:300071	Night blindness, congenital stationary, type 2A		HP:0000577	PMID:9662399	PCS		2/7			P	HPO:probinson[2022-09-03]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000286	PMID:26130459	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0001156	PMID:26130459	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0004322	OMIM:617088	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0002164	OMIM:617088	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0030674	PMID:26077881	PCS		3/3			C	HPO:probinson[2021-07-01]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000161	PMID:26130459	PCS		2/3			P	HPO:probinson[2022-05-28];HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0002240	OMIM:617088	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000085	OMIM:617088	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0010566	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0011461	PMID:26130459	PCS		3/3			C	HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0006695	PMID:26130459	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0008753	PMID:26130459	PCS		1/3			P	HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0001643	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000774	PMID:26077881;PMID:26130459	PCS		9/9			P	HPO:probinson[2022-05-28];HPO:probinson[2021-07-01]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000894	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000773	OMIM:617088	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0001744	OMIM:617088	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0003026	PMID:26077881;PMID:26130459	PCS		6/6			P	HPO:probinson[2022-05-28];HPO:probinson[2021-07-01]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000494	PMID:26130459	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0001561	PMID:26130459;OMIM:617088	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0002098	OMIM:617088	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0001162	PMID:26077881	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-01]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0001680	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000191	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0011069	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0005280	OMIM:617088	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0010579	PMID:26130459	PCS		2/2			P	HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0100259	PMID:26130459	PCS		3/3			P	HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0030010	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000668	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000888	PMID:26077881	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-01]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000007	PMID:26077881	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-01]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000369	PMID:26130459	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-28]
OMIM:617088	Short-rib thoracic dysplasia 15 with polydactyly		HP:0000148	OMIM:617088	IEA					P	HPO:skoehler[2018-10-08]
OMIM:131200	Endometriosis, susceptibility to, 1		HP:0030127	OMIM:131200	TAS					P	HPO:skoehler[2014-09-21]
OMIM:131200	Endometriosis, susceptibility to, 1		HP:0000144	OMIM:131200	IEA					P	HPO:iea[2009-02-17]
OMIM:131200	Endometriosis, susceptibility to, 1		HP:0000007	OMIM:131200	IEA					I	HPO:iea[2009-02-17]
OMIM:131200	Endometriosis, susceptibility to, 1		HP:0001426	OMIM:131200	IEA					I	HPO:iea[2009-02-17]
OMIM:131200	Endometriosis, susceptibility to, 1		HP:0100607	OMIM:131200	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002740	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0007417	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002741	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002202	PMID:24991462	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002840	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002240	PMID:24991462	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0100750	PMID:24991462	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0100523	OMIM:306400	TAS					P	HPO:probinson[2017-09-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0011463	PMID:24991462	PCS		1/1			C	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002716	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002955	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0006532	PMID:24991462	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0001945	PMID:24991462	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0003206	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0005406	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0001744	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002754	PMID:24991462	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0003621	OMIM:306400	IEA					C	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0003203	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0005224	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0001541	PMID:24991462	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0012735	PMID:24991462	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0001419	PMID:2556453	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0032252	PMID:24991462	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0033662	PMID:24991462	PCS		1/1			P	HPO:probinson[2022-04-04]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0100658	OMIM:306400	TAS					P	HPO:probinson[2017-09-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002726	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0000964	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002724	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0003514	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002723	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002742	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002842	OMIM:306400	IEA					P	HPO:iea[2009-02-17]
OMIM:306400	Chronic granulomatous disease, X-linked		HP:0002721	OMIM:306400	TAS					P	HPO:skoehler[2018-10-08]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0001276	OMIM:182960	IEA					P	HPO:iea[2009-02-17]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0003676	OMIM:182960	IEA					C	HPO:iea[2009-02-17]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0001761	OMIM:182960	IEA					P	HPO:iea[2009-02-17]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0003487	OMIM:182960	IEA					P	HPO:iea[2009-02-17]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0003484	OMIM:182960	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2012-03-13]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0003693	OMIM:182960	PCS					P	HPO:probinson[2012-03-13]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0006938	OMIM:182960	PCS					P	HPO:probinson[2012-03-13]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0002460	OMIM:182960	PCS					P	HPO:probinson[2012-03-13]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0007267	OMIM:182960	IEA					P	HPO:iea[2009-02-17]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0000006	OMIM:182960	TAS					I	HPO:probinson[2012-04-11]
OMIM:182960	Neuronopathy, distal hereditary motor, type I		HP:0001765	OMIM:182960	IEA					P	HPO:iea[2009-02-17]
OMIM:614595	Preeclampsia/eclampsia 5		HP:0100602	PMID:22437503	PCS			FEMALE		H	HPO:skoehler[2015-01-27];HPO:probinson[2020-07-21]
OMIM:614595	Preeclampsia/eclampsia 5		HP:0003581	PMID:22437503	PCS					C	HPO:probinson[2021-10-13]
OMIM:614595	Preeclampsia/eclampsia 5		HP:0000006	PMID:22437503	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2021-10-13]
OMIM:206400	Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrinmetabolism		HP:0003163	OMIM:206400	IEA					P	HPO:iea[2009-02-17]
OMIM:206400	Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrinmetabolism		HP:0000007	OMIM:206400	IEA					I	HPO:iea[2009-02-17]
OMIM:206400	Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrinmetabolism		HP:0000952	OMIM:206400	IEA					P	HPO:iea[2009-02-17]
OMIM:206400	Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrinmetabolism		HP:0001744	OMIM:206400	IEA					P	HPO:iea[2009-02-17]
OMIM:206400	Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrinmetabolism		HP:0001930	OMIM:206400	IEA					P	HPO:iea[2009-02-17]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0002135	PMID:8733126;PMID:8813042	PCS		3/27			P	HPO:probinson[2021-09-06];HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0000121	PMID:8733126;PMID:8813042	PCS		12/27			P	HPO:probinson[2021-09-06];HPO:probinson[2021-09-06];HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0003401	PMID:8733126	PCS		3/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0003621	PMID:8733126	PCS		1/7			C	HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0004322	OMIM:601198	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0001250	PMID:8733126;PMID:8813042	PCS		9/27			P	HPO:probinson[2021-09-06];HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0031817	PMID:8733126	PCS		2/7			P	HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0003394	PMID:8733126	PCS		7/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0002150	PMID:8813042	PCS		9/20			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0001281	PMID:7874174	PCS		1/14			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0012213	PMID:8813042	PCS		2/20			P	HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0002917	PMID:8813042	PCS		16/20			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0000848	OMIM:601198	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0011463	PMID:8733126	PCS		5/7			C	HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0011462	PMID:8733126	PCS		1/7			C	HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0002905	PMID:8733126	PCS		5/7			P	HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0002900	OMIM:601198	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0025425	PMID:8733126	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0002901	PMID:8733126;PMID:7874174;PMID:8813042	PCS		41/41			P	HPO:probinson[2021-09-06];HPO:skoehler[2015-01-27];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0000006	PMID:7874174	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:601198	Hypocalcemia, autosomal dominant 1		HP:0000787	PMID:8813042	PCS		4/20			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-09-06]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0002345	OMIM:300703	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0000639	PMID:18241076	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0001260	PMID:18241076	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0001419	PMID:18241076	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0003680	PMID:18241076	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0001251	PMID:18241076	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0001270	PMID:18241076	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0001319	PMID:18241076	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0001249	PMID:18241076	PCS		0/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:300703	Spinocerebellar ataxia, X-linked 5		HP:0003623	PMID:18241076	PCS		6/6			C	HPO:probinson[2024-03-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000341	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0003577	PMID:36228617	PCS		5/5			C	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000343	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0001156	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0001250	PMID:36228617	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0001252	PMID:36228617	PCS		1/5			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0001274	PMID:36228617	PCS		1/5			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0010963	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000319	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000238	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0002119	PMID:36228617	PCS		2/4			P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000218	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000278	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0002059	PMID:36228617	PCS		1/5			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0002595	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0030048	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0002079	PMID:36228617	PCS		3/5			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0001263	PMID:36228617	PCS		2/2			P	HPO:probinson[2023-04-09];HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000470	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0045025	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0010636	PMID:36228617	PCS		1/5			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0034295	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0002803	PMID:36228617	PCS		1/5			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000007	PMID:36228617	PCS					I	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000601	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0002705	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000664	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000322	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0001510	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0002126	PMID:36228617	PCS		2/5			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000347	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:620156	Cortical dysplasia, complex, with other brain malformations 11		HP:0000369	PMID:36228617	PCS		1/4			P	HPO:probinson[2023-04-09]
OMIM:617275	Tooth agenesis, selective, 9		HP:0000691	PMID:26416033	PCS		1/7			P	HPO:probinson[2023-02-24]
OMIM:617275	Tooth agenesis, selective, 9		HP:0001592	PMID:26416033	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617275	Tooth agenesis, selective, 9		HP:0000679	PMID:26416033	PCS		1/7			P	HPO:probinson[2023-02-24]
OMIM:617275	Tooth agenesis, selective, 9		HP:0000006	PMID:26416033	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-24]
OMIM:619258	Spermatogenic failure 53		HP:0003251	PMID:33626338	PCS		3/3			P	HPO:probinson[2021-05-29]
OMIM:619258	Spermatogenic failure 53		HP:0032562	PMID:33626338	PCS		3/3			P	HPO:probinson[2021-05-29]
OMIM:619258	Spermatogenic failure 53		HP:0000007	PMID:33626338	PCS					I	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:613013	Neuroblastoma, susceptibility to, 2		HP:0003005	OMIM:613013	TAS		5%			P	HPO:probinson[2013-04-14]
OMIM:613013	Neuroblastoma, susceptibility to, 2		HP:0006747	OMIM:613013	TAS		5%			P	HPO:probinson[2013-04-14]
OMIM:613013	Neuroblastoma, susceptibility to, 2		HP:0002251	OMIM:613013	TAS		HP:0040283			P	HPO:probinson[2013-04-14]
OMIM:613013	Neuroblastoma, susceptibility to, 2		HP:0003006	OMIM:613013	TAS		5%			P	HPO:probinson[2013-01-09]
OMIM:613013	Neuroblastoma, susceptibility to, 2		HP:0000006	OMIM:613013	TAS					I	HPO:probinson[2013-04-14]
OMIM:268130	Revesz syndrome		HP:0001276	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0002344	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0007617	PMID:18252230	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:268130	Revesz syndrome		HP:0000485	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0001251	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0003593	PMID:21477109	PCS		1/1			C	HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0008070	OMIM:268130	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268130	Revesz syndrome		HP:0000639	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0011463	PMID:18252230	PCS		1/1			C	HPO:probinson[2022-07-01]
OMIM:268130	Revesz syndrome		HP:0001803	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0005528	PMID:21477109	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:268130	Revesz syndrome		HP:0003745	OMIM:268130	IEA					I	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0002514	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0000555	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0002311	PMID:21477109	PCS		1/1			P	HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0000572	PMID:21477109	PCS		1/1			P	HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0002136	PMID:21477109	PCS		1/1			P	HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0002213	OMIM:268130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:268130	Revesz syndrome		HP:0000252	PMID:21477109	PCS		1/1			P	HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0001321	PMID:21477109;PMID:18252230	PCS		2/2			P	HPO:probinson[2024-02-17];HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:268130	Revesz syndrome		HP:0001263	PMID:21477109;PMID:18252230	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01];HPO:skoehler[2019-02-22];HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0031413	PMID:21477109;PMID:18252230	PCS		2/2			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01];HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0001915	PMID:18252230	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:268130	Revesz syndrome		HP:0008402	OMIM:268130	TAS					P	HPO:skoehler[2013-05-31]
OMIM:268130	Revesz syndrome		HP:0001511	OMIM:268130	IEA					P	HPO:iea[2009-02-17]
OMIM:268130	Revesz syndrome		HP:0008404	PMID:21477109;PMID:18252230	PCS		2/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-07-01];HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0007898	PMID:21477109;PMID:18252230	PCS		2/2			P	HPO:probinson[2024-02-17];HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:268130	Revesz syndrome		HP:0001972	PMID:21477109	PCS		1/1			P	HPO:probinson[2024-02-17]
OMIM:268130	Revesz syndrome		HP:0002745	PMID:21477109;PMID:18252230	PCS		2/2			P	HPO:probinson[2024-02-17];HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:268130	Revesz syndrome		HP:0000006	PMID:18252230	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:268130	Revesz syndrome		HP:0001875	PMID:21477109	PCS		1/1			P	HPO:probinson[2024-02-17]
OMIM:156700	Microcornea, glaucoma, and absent frontal sinuses		HP:0000482	OMIM:156700	IEA					P	HPO:iea[2009-02-17]
OMIM:156700	Microcornea, glaucoma, and absent frontal sinuses		HP:0000006	OMIM:156700	IEA					I	HPO:iea[2009-02-17]
OMIM:156700	Microcornea, glaucoma, and absent frontal sinuses		HP:0000501	OMIM:156700	IEA					P	HPO:iea[2009-02-17]
OMIM:156700	Microcornea, glaucoma, and absent frontal sinuses		HP:0002688	OMIM:156700	IEA					P	HPO:iea[2009-02-17]
OMIM:601371	Cataract, age-related nuclear		HP:0100018	OMIM:601371	TAS					P	HPO:probinson[2013-03-13]
OMIM:601371	Cataract, age-related nuclear		HP:0000007	OMIM:601371	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0003233	PMID:31358993	PCS		9/17			P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0002155	PMID:31358993	PCS		10/17			P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0003141	PMID:31358993	PCS		5/16			P	HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0000822	PMID:31358993	PCS		26/35			P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0001658	PMID:31358993	PCS		13/36			P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0040217	PMID:31358993	PCS		7/17			P	HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0005978	PMID:31358993	PCS					P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0000006	PMID:31358993	PCS					I	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0004943	PMID:31358993	PCS					P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0001513	PMID:31358993	PCS					P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618620	Abdominal obesity-metabolic syndrome 4		HP:0001677	PMID:31358993	PCS					P	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:617507	Peho-Like syndrome		HP:0000341	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000286	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0002069	PMID:26917597	PCS	HP:0011463	3/3			P	HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000340	PMID:26917597	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0002521	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0003577	PMID:26917597	PCS		3/3			C	HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001272	PMID:26917597	PCS		3/3		HP:0003676	P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0003196	PMID:26917597	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001252	PMID:26917597	PCS		3/3			P	HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0002119	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001302	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0007105	PMID:26917597	PCS				HP:0003676	P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000278	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001347	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000253	PMID:26917597	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0002133	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001344	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0002079	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000194	PMID:26917597	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000293	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0011968	PMID:26917597	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001182	PMID:26917597	PCS		3/3			P	HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0012736	PMID:26917597	PCS		3/3			P	HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000969	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001339	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0025405	PMID:26917597	PCS		3/3			P	HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000007	PMID:26917597	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0000648	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001319	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0002126	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617507	Peho-Like syndrome		HP:0001336	PMID:26917597	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0003388	OMIM:265400	IEA					P	HPO:iea[2012-04-11]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0001681	OMIM:265400	IEA					P	HPO:iea[2009-02-17]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0003593	PMID:34493544	PCS		1/5			C	HPO:probinson[2022-07-09]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0002092	PMID:34493544	PCS		5/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-07-09]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0012378	OMIM:265400	TAS					P	HPO:skoehler[2013-10-22]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0011463	PMID:34493544	PCS		3/5			C	HPO:probinson[2022-07-09]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0001708	PMID:34493544	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0000007	PMID:34493544	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-25]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0001324	OMIM:265400	IEA					P	HPO:iea[2009-02-17]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0001279	OMIM:265400	IEA					P	HPO:iea[2009-02-17]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0001667	PMID:34493544	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-09]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0002875	OMIM:265400	IEA					P	HPO:iea[2009-02-17]
OMIM:265400	Pulmonary hypertension, primary, autosomal recessive		HP:0003623	PMID:34493544	PCS		1/5			C	HPO:probinson[2022-07-09]
OMIM:212850	Cerebellar ataxia and neurosensory deafness		HP:0001761	OMIM:212850	IEA					P	HPO:iea[2009-02-17]
OMIM:212850	Cerebellar ataxia and neurosensory deafness		HP:0000407	OMIM:212850	IEA					P	HPO:iea[2009-02-17]
OMIM:212850	Cerebellar ataxia and neurosensory deafness		HP:0001251	OMIM:212850	IEA	HP:0003581				P	HPO:iea[2009-02-17]
OMIM:212850	Cerebellar ataxia and neurosensory deafness		HP:0000007	OMIM:212850	IEA					I	HPO:iea[2009-02-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0003676	PMID:19068277	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0000486	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001310	PMID:19068277	PCS					P	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001332	PMID:19068277	PCS		7/9			P	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001272	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001250	PMID:19068277	PCS		2/9			P	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0000020	OMIM:612319	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001251	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0002061	PMID:19068277	PCS		9/9			P	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0002180	OMIM:612319	IEA					P	HPO:skoehler[2015-01-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0033725	PMID:19068277	PCS		3/9			P	HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0000639	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0011463	PMID:19068277	PCS		7/9			C	HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0002518	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0007366	OMIM:612319	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001268	PMID:19068277	PCS					P	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001249	OMIM:612319	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001347	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0006978	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0003621	PMID:19068277	PCS		2/9			C	HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0003487	PMID:19068277	PCS	HP:0003621				P	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001288	PMID:19068277	PCS		9/9			P	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0002079	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0000012	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001260	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001285	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0002075	PMID:19068277	PCS					P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0011448	OMIM:612319	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0000007	PMID:19068277	PCS					I	HPO:probinson[2012-04-17];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0000648	OMIM:612319	TAS					P	HPO:probinson[2012-04-17]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0001258	PMID:19068277	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-03-21]
OMIM:612319	Spastic paraplegia 35, autosomal recessive		HP:0000544	OMIM:612319	TAS		HP:0040283			P	HPO:probinson[2012-04-17]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0002553	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001265	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001562	PMID:23932106	PCS		1/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0000494	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001561	PMID:23932106	PCS		1/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0002353	OMIM:615476	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001344	PMID:23932106	PCS		2/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0002197	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0002121	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001252	OMIM:615476	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001252	PMID:23932106	PCS	HP:0003593	2/2			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0003593	PMID:23932106	PCS		3/3			C	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0012736	PMID:23932106	PCS		3/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0007270	PMID:23932106	PCS		1/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0007074	OMIM:615476	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0032792	PMID:23932106	PCS		1/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0000508	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0000007	PMID:23932106	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0000348	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0200134	OMIM:615476	IEA					P	HPO:skoehler[2015-01-19]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0007334	PMID:23932106	PCS		1/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001659	PMID:23932106	PCS		1/3			P	HPO:probinson[2023-03-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0007359	OMIM:615476	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615476	Developmental and epileptic encephalopathy 18		HP:0001631	PMID:23932106	PCS		1/3			P	HPO:probinson[2023-03-18]
OMIM:261100	Megaloblastic anemia 1		HP:0003401	OMIM:261100	IEA					P	HPO:iea[2009-02-17]
OMIM:261100	Megaloblastic anemia 1		HP:0100502	PMID:17285242	PCS					P	HP:probinson[2019-03-14]
OMIM:261100	Megaloblastic anemia 1		HP:0001289	OMIM:261100	IEA					P	HPO:iea[2009-02-17]
OMIM:261100	Megaloblastic anemia 1		HP:0200118	PMID:17285242	PCS					P	HPO:skoehler[2013-06-11];HP:probinson[2019-03-14]
OMIM:261100	Megaloblastic anemia 1		HP:0040087	PMID:21208123	PCS		0/1			P	HP:probinson[2019-03-14];HPO:probinson[2022-08-24]
OMIM:261100	Megaloblastic anemia 1		HP:0011463	OMIM:261100	TAS					C	HPO:probinson[2012-07-31]
OMIM:261100	Megaloblastic anemia 1		HP:0000726	OMIM:261100	IEA					P	HPO:iea[2009-02-17]
OMIM:261100	Megaloblastic anemia 1		HP:0002907	PMID:21208123	PCS		1/1			P	HPO:probinson[2022-08-24]
OMIM:261100	Megaloblastic anemia 1		HP:0003474	OMIM:261100	IEA					P	HPO:iea[2009-02-17]
OMIM:261100	Megaloblastic anemia 1		HP:0001889	PMID:21208123	PCS		1/1			P	HPO:probinson[2012-07-31];HP:probinson[2019-03-14];HPO:probinson[2022-08-24]
OMIM:261100	Megaloblastic anemia 1		HP:0000007	PMID:10080186	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:261100	Megaloblastic anemia 1		HP:0000093	PMID:21208123	PCS		1/1			P	HPO:iea[2009-02-17];HP:probinson[2019-03-14];HPO:probinson[2022-08-24]
OMIM:618152	Spermatogenic failure 33		HP:0033393	PMID:30122540	PCS		6/6			P	HPO:probinson[2023-02-25]
OMIM:618152	Spermatogenic failure 33		HP:0032560	PMID:30122540	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-25]
OMIM:618152	Spermatogenic failure 33		HP:0003251	PMID:30122540	PCS		7/7			P	HPO:probinson[2023-02-25]
OMIM:618152	Spermatogenic failure 33		HP:0011462	PMID:30122540	PCS		7/7			C	HPO:probinson[2023-02-25]
OMIM:618152	Spermatogenic failure 33		HP:0000007	PMID:30122540	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:618152	Spermatogenic failure 33		HP:0012207	PMID:30122540	PCS		7/7			P	HPO:probinson[2023-02-25]
OMIM:618152	Spermatogenic failure 33		HP:0032558	PMID:30122540	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-25]
OMIM:618152	Spermatogenic failure 33		HP:0032559	PMID:30122540	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-25]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000750	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0002373	PMID:32869858	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0001260	PMID:32869858	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0001263	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0100033	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0031987	PMID:32869858	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000639	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0011463	PMID:32869858	PCS		2/2			C	HPO:probinson[2021-06-26]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000739	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000007	PMID:32869858	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000337	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000678	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0025116	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0001357	PMID:32869858	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000664	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0002007	PMID:32869858	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0001007	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619264	Neurodevelopmental disorder with dysmorphic facies and variable seizures		HP:0000325	PMID:32869858	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0001360	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=anophthalmia-ov	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0000528	PMID:12503095	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0003828	OMIM:611638	PCS					M	HPO:iea[2009-11-30]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0003829	OMIM:611638	PCS					I	HPO:iea[2009-02-17]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0000612	PMID:12503095	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0000568	OMIM:611638	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0000504	PMID:12503095	PCS		HP:0040282			P	HPO:iea[2009-11-30]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0000202	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=anophthalmia-ov	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0007633	OMIM:611638	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0000006	PMID:12503095	PCS					I	HPO:iea[2009-02-17]
OMIM:611638	Microphthalmia, isolated, with coloboma 5		HP:0000567	PMID:12503095	PCS					P	HPO:probinson[2017-12-13]
OMIM:264050	Prenatal bowing		HP:0000007	OMIM:264050	IEA					I	HPO:iea[2009-02-17]
OMIM:264050	Prenatal bowing		HP:0006487	OMIM:264050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:264050	Prenatal bowing		HP:0000951	OMIM:264050	IEA					P	HPO:iea[2009-02-17]
OMIM:616631	Porokeratosis 9, multiple types		HP:0003621	PMID:26202976	PCS		1/4			C	HPO:probinson[2023-03-26]
OMIM:616631	Porokeratosis 9, multiple types		HP:0003596	PMID:26202976	PCS		2/4			C	HPO:probinson[2023-03-26]
OMIM:616631	Porokeratosis 9, multiple types		HP:0011462	PMID:26202976	PCS		1/4			C	HPO:probinson[2023-03-26]
OMIM:616631	Porokeratosis 9, multiple types		HP:0200044	PMID:26202976	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-26]
OMIM:616631	Porokeratosis 9, multiple types		HP:0000006	PMID:26202976	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:620383	Oocyte/zygote/embryo maturation arrest 20		HP:0008222	PMID:34779126	PCS		3/3			P	HPO:probinson[2023-07-17]
OMIM:620383	Oocyte/zygote/embryo maturation arrest 20		HP:0011462	PMID:34779126	PCS		3/3			C	HPO:probinson[2023-07-17]
OMIM:620383	Oocyte/zygote/embryo maturation arrest 20		HP:0000141	PMID:34779126	PCS		0/3			P	HPO:probinson[2023-07-17]
OMIM:620383	Oocyte/zygote/embryo maturation arrest 20		HP:0000007	PMID:34779126	PCS					I	HPO:probinson[2023-07-17]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0000572	OMIM:615338	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0002059	PMID:23526554	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0000252	OMIM:615338	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0003676	OMIM:615338	TAS					C	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0002133	OMIM:615338	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0002376	PMID:23526554	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0001332	OMIM:615338	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0011968	PMID:23526554	PCS		1/1			P	HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0001263	PMID:23526554;OMIM:615338	PCS		12/12		HP:0012828	P	HPO:skoehler[2019-02-22];HPO:skoehler[2013-10-06];HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0006829	OMIM:615338	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0001252	PMID:23526554	PCS		2/2			P	HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0005484	OMIM:615338	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0003593	PMID:23526554	PCS		2/2			C	HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0012448	OMIM:615338	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0002071	OMIM:615338	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0033258	PMID:23526554	PCS		1/2			P	HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0000007	PMID:23526554	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0020221	PMID:23526554	PCS		2/2			P	HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0200134	PMID:23526554	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-13]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0000648	OMIM:615338	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0001269	OMIM:615338	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615338	Developmental and epileptic encephalopathy 16		HP:0001336	OMIM:615338	TAS					P	HPO:skoehler[2013-10-06]
OMIM:613985	BETA-THALASSEMIA		HP:0011906	OMIM:613985	TAS					P	HPO:probinson[2013-02-17]
OMIM:613985	BETA-THALASSEMIA		HP:0004840	OMIM:613985	TAS					P	HPO:probinson[2013-02-17]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0007083	PMID:26072516	PCS					P	HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0003376	PMID:26072516	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0001288	PMID:26072516	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0001761	PMID:26072516	TAS					P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0003693	PMID:26072516	PCS					P	HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0003828	OMIM:616625	TAS					M	HPO:skoehler[2017-07-13]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0002460	PMID:26072516	PCS					P	HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0009830	OMIM:616625	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0002936	PMID:26072516	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0003438	PMID:26072516	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0000006	PMID:26072516	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-10]
OMIM:616625	Charcot-Marie-Tooth disease, axonal, type 2W		HP:0001765	PMID:26072516	TAS					P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-10]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000582	PMID:31512373	PCS		3/3			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000692	PMID:31512373	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000750	PMID:31512373	PCS		4/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000574	PMID:31512373	PCS		2/3			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0002650	PMID:31512373	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000365	PMID:31512373	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000463	PMID:31512373	PCS		3/3			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0001290	PMID:31512373	PCS		4/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0004691	PMID:31512373	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0001270	PMID:31512373	PCS					P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0011228	PMID:31512373	PCS		1/3			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0008872	PMID:31512373	IEA	HP:0003593	4/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000527	PMID:31512373	PCS		2/2			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000219	PMID:31512373	PCS		3/3			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0009237	PMID:31512373	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0004209	PMID:31512373	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000006	PMID:31512373	PCS					I	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0001007	PMID:31512373	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000369	PMID:31512373	PCS		4/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0000347	PMID:31512373	PCS		4/4			P	HPO:probinson[2020-07-17]
OMIM:618608	Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies		HP:0001611	PMID:31512373	PCS		3/4			P	HPO:probinson[2020-07-17]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0003577	PMID:16951682	PCS		10/10			C	HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0003431	PMID:17683097	PCS		9/10			P	HPO:probinson[2012-07-16];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0004466	PMID:17683097	PCS		7/10			P	HPO:probinson[2024-02-27]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001250	PMID:16951682	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0100291	PMID:17683097	PCS		6/10			P	HPO:probinson[2024-02-27]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001271	PMID:16951682	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001270	PMID:17683097	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0002080	PMID:17683097	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0007340	PMID:17683097	PCS		9/10			P	HPO:probinson[2012-07-16];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0000519	PMID:16951682	PCS	HP:0003577	10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0003429	PMID:17683097	PCS		10/10			P	HPO:probinson[2022-09-21];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0002415	PMID:17683097	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001249	PMID:16951682	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001347	PMID:17683097	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0008936	PMID:17683097	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0002650	PMID:16951682	PCS		4/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0003487	PMID:17683097	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0031936	PMID:16951682	PCS		3/10			P	HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0030147	PMID:17683097	PCS		9/10			P	HPO:skoehler[2014-10-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001260	PMID:17683097	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001263	PMID:16951682	PCS		10/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0003383	PMID:17683097	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0012762	PMID:17683097	PCS				HP:0003676	P	HPO:skoehler[2014-04-13];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0007210	PMID:17683097	PCS		9/10			P	HPO:probinson[2012-07-16];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0001317	OMIM:610532	IEA					P	HPO:iea[2009-02-17]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0000007	PMID:16951682	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0007256	PMID:16951682	PCS		9/10			P	HPO:probinson[2022-09-21]
OMIM:610532	Leukodystrophy, hypomyelinating, 5		HP:0002505	PMID:17683097	PCS	HP:0003621	5/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-21]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0002069	PMID:15609246	PCS		2/2			P	HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0002521	PMID:15609246	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0002188	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0001250	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0001252	PMID:15609246	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0003593	PMID:15609246	PCS		2/2			C	HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0003150	OMIM:600721	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0032794	PMID:15609246	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0012469	PMID:15609246	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0100704	PMID:15609246	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0011220	PMID:15609246	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0002416	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0007105	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0001324	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0000256	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0001249	OMIM:600721	IEA					P	HPO:skoehler[2010-06-18]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0005348	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0006956	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0002572	PMID:15609246	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:6000246	PMID:20020533;OMIM:600721	PCS		20/20			P	HPO:probinson[2024-05-09];HPO:probinson[2024-02-27]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0001263	PMID:15609246	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0012321	PMID:15609246	PCS		2/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0007052	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0032792	PMID:15609246	PCS		1/2			P	HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0000007	PMID:15609246	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0001638	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0001659	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0002007	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0002104	OMIM:600721	IEA					P	HPO:iea[2009-02-17]
OMIM:600721	D-2-Hydroxyglutaric aciduria 1		HP:0000347	PMID:15609246	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
DECIPHER:8	Smith-Magenis syndrome		HP:0001156	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:8	Smith-Magenis syndrome		HP:0004322	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:8	Smith-Magenis syndrome		HP:0001609	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:8	Smith-Magenis syndrome		HP:0001252	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:8	Smith-Magenis syndrome		HP:0000733	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:8	Smith-Magenis syndrome		HP:0000752	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:8	Smith-Magenis syndrome		HP:0001249	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:8	Smith-Magenis syndrome		HP:0000742	DECIPHER:8	IEA					P	HPO:skoehler[2013-05-29]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000054	PMID:18252794	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0003577	PMID:18252794	PCS		4/4			C	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0008707	OMIM:201810	TAS					P	HPO:skoehler[2017-07-13]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000051	PMID:18252794	PCS		1/4			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0002153	PMID:18252794	PCS		3/4			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000062	OMIM:201810	TAS					P	HPO:skoehler[2017-07-13]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0033809	PMID:18252794	PCS		3/6			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0031078	PMID:18252794	PCS		2/3			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0031213	PMID:18252794	PCS		4/4			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0034589	PMID:18252794	PCS		3/3			P	HPO:probinson[2023-03-31]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0012411	OMIM:201810	TAS					P	HPO:skoehler[2017-07-13]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0012853	PMID:18252794	PCS		1/4			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000808	PMID:18252794	PCS		1/4			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0008221	OMIM:201810	IEA					P	HPO:skoehler[2013-01-09]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0002902	PMID:18252794	PCS		3/4			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000007	PMID:1363812	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000846	PMID:18252794	PCS		1/4			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0030260	PMID:18252794	PCS		1/4			P	HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000037	OMIM:201810	IEA			MALE		P	HPO:skoehler[2013-01-09]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000048	PMID:18252794	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000047	OMIM:201810	IEA			MALE		P	HPO:skoehler[2013-01-09]
OMIM:201810	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency		HP:0000028	PMID:18252794	PCS		2/4			P	HPO:probinson[2023-02-22]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0001531	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0005994	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0003198	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0001252	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0001290	OMIM:162300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0003307	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0000218	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0003528	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0000179	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002019	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002014	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0003005	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0000574	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002650	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0001761	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0001382	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002253	OMIM:162300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0001263	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002251	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0001519	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002808	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0031284	OMIM:162300	TAS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-04]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0006461	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0000767	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0003639	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002705	OMIM:162300	TAS					P	HPO:skoehler[2015-12-30]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002865	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0000006	PMID:7906866	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-04]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0008208	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:162300	Multiple endocrine neoplasia, type IIB		HP:0002666	OMIM:162300	IEA					P	HPO:iea[2009-02-17]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0000750	PMID:28868155	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0002188	PMID:28868155	PCS		1/2			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0034295	PMID:28868155	PCS		1/2			P	HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0001250	PMID:28868155	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0001263	PMID:28868155	PCS		2/2			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0032388	PMID:28868155	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0001257	PMID:28868155	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0000006	PMID:28868155	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-12]
OMIM:618185	Periventricular nodular heterotopia 8		HP:0006855	PMID:28868155	PCS		1/2			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0002058	OMIM:616816	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0006956	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0000486	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0000750	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0002079	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0000276	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0000194	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0003198	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0001263	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0006829	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0001629	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0000007	PMID:26358778	PCS					I	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0001558	OMIM:616816	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0001319	OMIM:616816	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0002747	OMIM:616816	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0006897	OMIM:616816	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0000028	PMID:26358778	PCS					P	HPO:probinson[2017-06-17]
OMIM:616816	Hypotonia, infantile, with psychomotor retardation		HP:0003557	OMIM:616816	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0007626	OMIM:166600	IEA					P	HPO:iea[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0005106	OMIM:166600	IEA					P	HPO:iea[2013-04-04]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0000572	OMIM:166600	TAS					P	HPO:skoehler[2017-07-13]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0003148	OMIM:166600	IEA					P	HPO:iea[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0003621	OMIM:166600	IEA					C	HPO:iea[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0007209	OMIM:166600	IEA					P	HPO:iea[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0010628	OMIM:166600	TAS					P	HPO:skoehler[2014-11-26]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0003084	OMIM:166600	IEA					P	HPO:iea[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0011002	OMIM:166600	TAS					P	HPO:skoehler[2015-01-21]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0002757	OMIM:166600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0005528	OMIM:166600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0008843	OMIM:166600	IEA					P	HPO:iea[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0000006	PMID:11741829	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0002644	OMIM:166600	IEA					P	HPO:iea[2009-02-17]
OMIM:166600	Osteopetrosis, autosomal dominant 2		HP:0005789	OMIM:166600	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000187	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0003015	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0010628	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000431	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0005465	PMID:23951358	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000280	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0100255	OMIM:218400	IEA					P	HPO:skoehler[2015-01-27]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0001739	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000506	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0006384	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0009772	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000316	PMID:23951358	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000007	PMID:23951358	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000648	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0004407	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0001742	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000696	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000256	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000410	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000765	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0001249	PMID:23951358	PCS		0/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000303	OMIM:218400	IEA					P	HPO:iea[2009-02-17]
OMIM:218400	Craniometaphyseal dysplasia, autosomal recessive		HP:0000457	PMID:23951358	PCS		5/5			P	HPO:probinson[2024-03-08]
OMIM:270970	Spherocytosis, autosomal recessive		HP:0004444	OMIM:270970	TAS					P	HPO:probinson[2012-05-05]
OMIM:270970	Spherocytosis, autosomal recessive		HP:0001878	OMIM:270970	TAS				HP:0012828	P	HPO:probinson[2012-05-05]
OMIM:270970	Spherocytosis, autosomal recessive		HP:0000007	OMIM:270970	TAS					I	HPO:probinson[2012-05-05]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0002540	PMID:27013236	PCS		1/1			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0001344	PMID:27013236	PCS		1/1			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0003819	PMID:27013236	PCS		1/2			C	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0011968	PMID:27013236	PCS		1/1			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0002352	PMID:27013236	PCS		2/2			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0000020	PMID:27013236	PCS		1/1			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0000007	PMID:27013236	PCS					I	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0002757	PMID:27013236	PCS		1/2			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0001511	PMID:27013236	PCS		2/2			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0002514	PMID:27013236	PCS		2/2			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0001147	PMID:27013236	PCS		2/2			P	HPO:probinson[2023-07-24]
OMIM:620368	Cerebroretinal microangiopathy with calcifications and cysts 3		HP:0002239	PMID:27013236	PCS		1/2			P	HPO:probinson[2023-07-24]
OMIM:255500	Myopia, infantile severe		HP:0000007	OMIM:255500	IEA					I	HPO:iea[2009-02-17]
OMIM:255500	Myopia, infantile severe		HP:0000545	OMIM:255500	IEA					P	HPO:skoehler[2009-02-17]
OMIM:183840	Spondyloarthropathy, susceptibility to, 2		HP:0001939	OMIM:183840	IEA					P	HPO:iea[2009-02-17]
OMIM:183840	Spondyloarthropathy, susceptibility to, 2		HP:0001367	OMIM:183840	IEA					P	HPO:iea[2009-02-17]
OMIM:183840	Spondyloarthropathy, susceptibility to, 2		HP:0000006	OMIM:183840	IEA					I	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001254	PMID:34668645	PCS		76/266			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0003774	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002188	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001970	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001250	PMID:34668645	PCS		58/266			P	HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001252	PMID:7681251	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002240	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0003593	PMID:7681251	PCS		3/10			C	HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001508	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0011463	PMID:7681251	PCS		2/10			C	HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001944	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001987	PMID:1977311	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001943	PMID:1977311	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002912	PMID:1977311	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001324	PMID:34668645	PCS		63/266			P	HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0004911	PMID:1977311	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0003623	PMID:7681251;PMID:1977311	PCS		6/11			C	HPO:probinson[2022-04-30];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002014	PMID:34668645	PCS		47/266			P	HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002453	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001882	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002013	PMID:34668645	PCS		81/266			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002098	PMID:1977311	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0011968	PMID:34668645	PCS		124/266			P	HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0002154	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001263	PMID:7681251	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0040126	PMID:34668645	PCS		0/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0011695	OMIM:251000	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0012120	PMID:34668645;PMID:1977311	PCS		267/267			P	HPO:probinson[2024-03-16];HPO:skoehler[2012-10-17];HPO:probinson[2022-04-30]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0000007	OMIM:251000	IEA					I	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001638	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0005979	PMID:7681251	PCS		8/10			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001873	PMID:1977311	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001733	OMIM:251000	IEA					P	HPO:iea[2009-02-17]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001259	PMID:34668645	PCS		56/266			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251000	Methylmalonic aciduria, mut type		HP:0001875	PMID:1977311	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:254150	Musk, inability to smell		HP:0000618	OMIM:254150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254150	Musk, inability to smell		HP:0000007	OMIM:254150	IEA					I	HPO:iea[2009-02-17]
OMIM:254150	Musk, inability to smell		HP:0000458	OMIM:254150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300273	Goiter, multinodular 2		HP:0000866	OMIM:300273	IEA					P	HPO:iea[2009-02-17]
OMIM:300273	Goiter, multinodular 2		HP:0001423	OMIM:300273	IEA					I	HPO:iea[2009-02-17]
OMIM:219050	Cryptorchidism, unilateral or bilateral		HP:0012741	OMIM:219050	IEA					P	HPO:skoehler[2015-01-27]
OMIM:219050	Cryptorchidism, unilateral or bilateral		HP:0000028	OMIM:219050	IEA					P	HPO:iea[2009-02-17]
OMIM:219050	Cryptorchidism, unilateral or bilateral		HP:0000006	OMIM:219050	TAS					I	HPO:skoehler[2015-12-30]
OMIM:219050	Cryptorchidism, unilateral or bilateral		HP:0000104	OMIM:219050	IEA					P	HPO:iea[2009-02-17]
OMIM:314560	Von willebrand disease, X-linked form		HP:0001892	OMIM:314560	IEA					P	HPO:iea[2009-02-17]
OMIM:314560	Von willebrand disease, X-linked form		HP:0003010	OMIM:314560	IEA					P	HPO:iea[2009-02-17]
OMIM:314560	Von willebrand disease, X-linked form		HP:0001417	OMIM:314560	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:610283	Cone-Rod dystrophy 10		HP:0009926	PMID:16199541	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0007737	PMID:16199541	PCS					P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0000662	PMID:16199541	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0000529	PMID:16199541	PCS				HP:0003676	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0000608	PMID:16199541	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0000613	PMID:16199541	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0000007	PMID:16199541	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0007994	PMID:16199541	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0000510	PMID:16199541	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-01]
OMIM:610283	Cone-Rod dystrophy 10		HP:0007843	PMID:16199541	PCS					P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:128235	Dystonia 12		HP:0000473	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0002300	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0002015	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0003621	PMID:15260953;PMID:17282997	PCS		4/18			C	HPO:probinson[2022-03-21]
OMIM:128235	Dystonia 12		HP:0001300	PMID:17282997	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:128235	Dystonia 12		HP:0002067	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0001332	PMID:17282997	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:128235	Dystonia 12		HP:0002483	PMID:17282997	PCS		8/11			P	HPO:probinson[2022-03-21]
OMIM:128235	Dystonia 12		HP:0001260	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0002172	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0000716	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0011463	PMID:17282997	IEA		1/11			C	HPO:probinson[2022-03-21]
OMIM:128235	Dystonia 12		HP:0011462	PMID:15260953;PMID:17282997	PCS		13/18			C	HPO:probinson[2022-03-21];HPO:probinson[2009-02-17];HPO:probinson[2022-03-21]
OMIM:128235	Dystonia 12		HP:0000739	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0003829	OMIM:128235	IEA					I	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0000338	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0000712	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0002317	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0002307	OMIM:128235	IEA					P	HPO:iea[2009-02-17]
OMIM:128235	Dystonia 12		HP:0000006	PMID:15260953	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:128235	Dystonia 12		HP:0001337	PMID:17282997	PCS		5/11			P	HPO:probinson[2022-03-21]
OMIM:168605	Perry syndrome		HP:0002067	OMIM:168605	IEA					P	HPO:iea[2009-02-17]
OMIM:168605	Perry syndrome		HP:0002145	OMIM:168605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:168605	Perry syndrome		HP:0001332	PMID:24343258	PCS		2/8			P	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0002063	PMID:24343258	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0031589	PMID:24343258	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0000719	OMIM:168605	TAS					P	HPO:skoehler[2014-08-24]
OMIM:168605	Perry syndrome		HP:0100785	OMIM:168605	TAS					P	HPO:skoehler[2012-10-17]
OMIM:168605	Perry syndrome		HP:0000716	PMID:24343258	PCS		2/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0000739	PMID:24343258	PCS		2/6			P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0000734	PMID:24343258	PCS		2/5			P	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0001824	OMIM:168605	TAS					P	HPO:skoehler[2010-06-18]
OMIM:168605	Perry syndrome		HP:0001621	OMIM:168605	IEA					P	HPO:iea[2009-02-17]
OMIM:168605	Perry syndrome		HP:0000710	PMID:24343258	PCS		2/5			P	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0000511	OMIM:168605	TAS					P	HPO:skoehler[2014-08-24]
OMIM:168605	Perry syndrome		HP:0005943	PMID:24343258	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0002476	PMID:24343258	PCS		3/3			P	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0001300	PMID:24343258	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0000298	OMIM:168605	IEA					P	HPO:iea[2009-02-17]
OMIM:168605	Perry syndrome		HP:0002791	PMID:24343258	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0001260	OMIM:168605	IEA					P	HPO:iea[2009-02-17]
OMIM:168605	Perry syndrome		HP:0003581	PMID:24343258	PCS		6/6			C	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0002093	PMID:24343258	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0007110	OMIM:168605	TAS					P	HPO:skoehler[2010-06-20]
OMIM:168605	Perry syndrome		HP:0007311	OMIM:168605	IEA					P	HPO:iea[2009-02-17]
OMIM:168605	Perry syndrome		HP:0000741	PMID:24343258	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0002304	PMID:24343258	PCS		6/6			P	HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0001337	PMID:24343258	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0000006	PMID:19136952	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-04]
OMIM:168605	Perry syndrome		HP:0003678	OMIM:168605	TAS					C	HPO:skoehler[2010-06-19]
OMIM:600084	Macrocytosis, familial		HP:0001871	OMIM:600084	IEA					P	HPO:iea[2009-02-17]
OMIM:600084	Macrocytosis, familial		HP:0001939	OMIM:600084	IEA					P	HPO:iea[2009-02-17]
OMIM:600084	Macrocytosis, familial		HP:0000006	OMIM:600084	IEA					I	HPO:iea[2009-02-17]
OMIM:620354	Spermatogenic failure 83		HP:0034947	PMID:36792588	PCS		1/1			P	HPO:probinson[2023-07-18]
OMIM:620354	Spermatogenic failure 83		HP:0034011	PMID:36792588	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620354	Spermatogenic failure 83		HP:0003251	PMID:36792588	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620354	Spermatogenic failure 83		HP:0011462	PMID:36792588	PCS		1/1			C	HPO:probinson[2023-06-18]
OMIM:620354	Spermatogenic failure 83		HP:0000007	PMID:36792588	PCS					I	HPO:probinson[2023-06-18]
OMIM:620354	Spermatogenic failure 83		HP:0012207	PMID:36792588	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:610297	Parkinson disease 13		HP:0002067	PMID:15961413	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:610297	Parkinson disease 13		HP:0002063	PMID:15961413	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:610297	Parkinson disease 13		HP:0002548	PMID:15961413	PCS	HP:0003596				P	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:610297	Parkinson disease 13		HP:0000006	PMID:15961413	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:610297	Parkinson disease 13		HP:0001337	PMID:15961413	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2020-07-20]
OMIM:190800	TRISTICHIASIS		HP:0000006	OMIM:190800	IEA					I	HPO:iea[2009-02-17]
OMIM:190800	TRISTICHIASIS		HP:0008009	OMIM:190800	IEA					P	HPO:iea[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0003577	PMID:16962354	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0000252	PMID:16962354	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0001332	PMID:16962354	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0000161	PMID:16962354	PCS		2/2			P	HPO:skoehler[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0001250	PMID:16962354	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0005273	PMID:16962354	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0010757	PMID:16962354	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0005280	PMID:16962354	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0009099	PMID:16962354	PCS		2/2			P	HPO:probinson[2024-03-29]
OMIM:142946	Holoprosencephaly 4		HP:0000508	OMIM:142946	IEA					P	HPO:iea[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0000437	PMID:16962354	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0006870	PMID:16962354	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0000601	OMIM:142946	IEA					P	HPO:iea[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0002507	PMID:16962354	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0000873	PMID:16962354	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:142946	Holoprosencephaly 4		HP:0000006	OMIM:142946	IEA					I	HPO:iea[2009-02-17]
OMIM:142946	Holoprosencephaly 4		HP:0020128	PMID:16962354	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:178370	Pulmonary atresia with ventricular septal defect		HP:0001629	OMIM:178370	IEA					P	HPO:iea[2009-02-17]
OMIM:178370	Pulmonary atresia with ventricular septal defect		HP:0004935	OMIM:178370	IEA					P	HPO:iea[2009-02-17]
OMIM:178370	Pulmonary atresia with ventricular septal defect		HP:0000006	OMIM:178370	IEA					I	HPO:iea[2009-02-17]
OMIM:167250	Paget disease of bone 3		HP:0002653	OMIM:167250	TAS					P	HPO:iea[2013-04-02]
OMIM:167250	Paget disease of bone 3		HP:0000365	OMIM:167250	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:167250	Paget disease of bone 3		HP:0005686	OMIM:167250	TAS					P	HPO:iea[2013-04-02]
OMIM:167250	Paget disease of bone 3		HP:0003155	OMIM:167250	TAS					P	HPO:iea[2013-04-02]
OMIM:167250	Paget disease of bone 3		HP:0003084	OMIM:167250	TAS					P	HPO:iea[2013-04-02]
OMIM:167250	Paget disease of bone 3		HP:0002669	OMIM:167250	TAS					P	HPO:iea[2009-02-17]
OMIM:167250	Paget disease of bone 3		HP:0000006	OMIM:167250	TAS					I	HPO:iea[2009-02-17]
OMIM:167250	Paget disease of bone 3		HP:0002797	OMIM:167250	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001770	OMIM:607932	IEA					P	HPO:iea[2009-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000046	OMIM:607932	TAS					P	HPO:skoehler[2015-02-22]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000365	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0002188	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000089	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0004443	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0006829	OMIM:607932	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000482	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001252	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0010442	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000639	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000954	OMIM:607932	IEA					P	HPO:iea[2009-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000835	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000278	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000556	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000358	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000830	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001144	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000252	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000175	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000134	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001344	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000171	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001263	OMIM:607932;PMID:18252212	PCS		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0011800	OMIM:607932	TAS					P	HPO:skoehler[2013-11-28]
OMIM:607932	Microphthalmia, syndromic 6		HP:0010999	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000528	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0005819	PMID:18252212	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000568	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0006101	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000647	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0004209	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000400	OMIM:607932	TAS					P	HPO:skoehler[2012-10-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000369	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000248	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000006	PMID:18252212	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000324	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001155	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001156	OMIM:607932	TAS					P	HPO:skoehler[2014-11-26]
OMIM:607932	Microphthalmia, syndromic 6		HP:0002120	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001508	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000618	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0007068	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0002119	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000218	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0009600	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000411	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0010538	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001321	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0002011	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000193	OMIM:607932	IEA					P	HPO:iea[2009-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0009909	OMIM:607932	TAS					P	HPO:skoehler[2013-05-31]
OMIM:607932	Microphthalmia, syndromic 6		HP:0007370	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000821	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000348	OMIM:607932	IEA					P	HPO:iea[2009-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0001357	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000545	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000347	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000028	PMID:18252212	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000589	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:607932	Microphthalmia, syndromic 6		HP:0000864	PMID:18252212	PCS					P	HPO:iea[2012-04-24];HPO:probinson[2022-02-17]
OMIM:300500	Albinism, ocular, type I		HP:0000639	PMID:9529334	PCS		29/29			P	HPO:probinson[2009-02-17]
OMIM:300500	Albinism, ocular, type I		HP:0007680	OMIM:300500	IEA					P	HPO:probinson[2009-02-17]
OMIM:300500	Albinism, ocular, type I		HP:0001361	OMIM:300500	IEA					P	HPO:probinson[2009-02-17]
OMIM:300500	Albinism, ocular, type I		HP:0000613	PMID:9529334	PCS		29/29			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-09]
OMIM:300500	Albinism, ocular, type I		HP:0007750	PMID:9529334	PCS		29/29			P	HPO:probinson[2023-04-09]
OMIM:300500	Albinism, ocular, type I		HP:0001107	PMID:9529334	PCS		29/29			P	HPO:probinson[2009-02-17]
OMIM:300500	Albinism, ocular, type I		HP:0005592	PMID:9529334	PCS		10/12			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-09]
OMIM:300500	Albinism, ocular, type I		HP:0007663	PMID:9529334	PCS		29/29			P	HPO:probinson[2023-04-09]
OMIM:300500	Albinism, ocular, type I		HP:0001417	PMID:9529334	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-04-09]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000297	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0003621	OMIM:300266	IEA					C	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000486	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000012	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0003487	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0002362	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000020	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0002061	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0001419	OMIM:300266	TAS					I	HPO:probinson[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0007340	OMIM:300266	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0002839	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0007210	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0009882	OMIM:300266	TAS					P	HPO:probinson[2013-04-13]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000327	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000712	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000711	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000744	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0000505	OMIM:300266	TAS					P	HPO:probinson[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0002427	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0001258	OMIM:300266	IEA					P	HPO:skoehler[2015-01-27]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0001249	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0002445	OMIM:300266	TAS		20/20			P	HPO:probinson[2012-06-03];HPO:skoehler[2010-06-18]
OMIM:300266	Spastic paraplegia 16, X-linked		HP:0001347	OMIM:300266	IEA					P	HPO:iea[2009-02-17]
OMIM:606392	Maturity-onset diabetes of the young, type 4		HP:0004904	OMIM:606392	IEA					P	HPO:skoehler[2015-01-19]
OMIM:606392	Maturity-onset diabetes of the young, type 4		HP:0005978	OMIM:606392	TAS	HP:0011462				P	HPO:skoehler[2013-01-09]
OMIM:606392	Maturity-onset diabetes of the young, type 4		HP:0000006	OMIM:606392	TAS					I	HPO:skoehler[2013-02-24]
OMIM:133600	Exostoses of heel		HP:0100777	OMIM:133600	IEA					P	HPO:skoehler[2015-01-27]
OMIM:133600	Exostoses of heel		HP:0000924	OMIM:133600	IEA					P	HPO:iea[2009-02-17]
OMIM:133600	Exostoses of heel		HP:0000006	OMIM:133600	IEA					I	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0007814	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0001250	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0003198	OMIM:551500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0001263	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0001251	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0000639	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0000726	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0000618	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0001427	OMIM:551500	IEA					I	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0003737	OMIM:551500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0000510	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0000763	OMIM:551500	TAS					P	HPO:probinson[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0003701	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0000488	OMIM:551500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:551500	Neuropathy, ataxia, and retinitis pigmentosa		HP:0007117	OMIM:551500	IEA					P	HPO:iea[2009-02-17]
OMIM:200500	Acheiropody		HP:0005632	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0009828	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0003982	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0002990	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:200500	Acheiropody		HP:0004231	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0005792	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0010509	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0010048	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0004050	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0010744	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0010760	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-04-26]
OMIM:200500	Acheiropody		HP:0000007	PMID:11090342	PCS					I	HPO:iea[2009-02-17]
OMIM:200500	Acheiropody		HP:0009820	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0005736	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0003974	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:200500	Acheiropody		HP:0009802	OMIM:200500;PMID:11090342	PCS		HP:0040281			P	HPO:iea[2010-01-19]
OMIM:277950	Winchester syndrome		HP:0007957	PMID:16542393	PCS		0/2			P	HPO:skoehler[2015-08-22];HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0001495	PMID:16542393	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0001230	PMID:16542393	PCS		0/2			P	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0003593	PMID:16542393	PCS		1/2			C	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0001482	PMID:16542393	PCS		0/2			P	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0003040	PMID:16542393	PCS					P	HPO:skoehler[2015-08-22];HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0040160	PMID:16542393	PCS		2/2			P	HPO:skoehler[2015-08-22];HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0000280	PMID:16542393	PCS	HP:0011463	2/2			P	HPO:skoehler[2015-08-22];HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0002808	PMID:16542393	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0011463	PMID:16542393	PCS		1/2			C	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0000007	PMID:16542393	PCS					I	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0006234	PMID:16542393	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:277950	Winchester syndrome		HP:0000212	OMIM:277950	IEA					P	HPO:skoehler[2015-08-22]
OMIM:277950	Winchester syndrome		HP:0001007	PMID:16542393	PCS	HP:0011463	1/2			P	HPO:probinson[2022-04-10]
OMIM:614782	Tremor, hereditary essential, 4		HP:0002345	PMID:22863194	PCS					P	HPO:probinson[2020-02-02]
OMIM:614782	Tremor, hereditary essential, 4		HP:0002174	PMID:22863194	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2020-02-02]
OMIM:614782	Tremor, hereditary essential, 4		HP:0000006	PMID:22863194	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-02-02]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0002015	PMID:36333996	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0000252	PMID:36333996	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0003621	PMID:36333996	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0001266	PMID:36333996	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0031959	PMID:36333996	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0001260	PMID:36333996	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0001252	PMID:36333996	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0001251	PMID:36333996	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0002072	PMID:36333996	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0001270	PMID:36333996	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0010535	PMID:36333996	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0011463	PMID:36333996	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0000657	PMID:36333996	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0000007	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0002505	PMID:36333996	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0007325	PMID:36333996	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620427	Dystonia 37, early-onset, with striatal lesions		HP:0001249	PMID:36333996	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:121210	Febrile seizures, familial, 1		HP:0002069	OMIM:121210	IEA					P	HPO:iea[2009-02-17]
OMIM:121210	Febrile seizures, familial, 1		HP:0002373	OMIM:121210	IEA					P	HPO:iea[2009-02-17]
OMIM:121210	Febrile seizures, familial, 1		HP:0011463	OMIM:121210	IEA					C	HPO:iea[2009-02-17]
OMIM:121210	Febrile seizures, familial, 1		HP:0010819	OMIM:121210	IEA					P	HPO:iea[2009-02-17]
OMIM:121210	Febrile seizures, familial, 1		HP:0010818	OMIM:121210	IEA					P	HPO:iea[2009-02-17]
OMIM:121210	Febrile seizures, familial, 1		HP:0000006	OMIM:121210	IEA					I	HPO:iea[2009-02-17]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0002465	OMIM:309530	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0002069	PMID:29026562	PCS		1/1			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0000486	OMIM:309530	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0000750	PMID:29026562	PCS		1/1			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0000540	OMIM:309530	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0002376	PMID:29026562	PCS		1/1			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0001250	PMID:29026562;PMID:26793055	PCS		3/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-30];HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0010819	PMID:29026562	PCS		1/1			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0005484	OMIM:309530	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0003593	PMID:29026562	PCS		1/1			C	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0001290	OMIM:309530	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0001419	OMIM:309530	IEA					I	HPO:iea[2009-02-17]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0000718	PMID:26793055	PCS		3/12			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0000729	PMID:29026562;PMID:26793055	PCS		3/13			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0008763	PMID:29026562	PCS		1/1			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0001423	PMID:26793055	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0001249	PMID:26793055	PCS		5/6	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0001249	PMID:26793055	PCS		4/6	FEMALE		P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0001249	PMID:29026562	PCS		1/1			P	HPO:probinson[2021-08-30]
OMIM:309530	Intellectual developmental disorder, X-linked 1		HP:0000248	OMIM:309530	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618806	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant		HP:0005403	PMID:31447097	PCS	HP:0003577	21/21			P	HPO:probinson[2020-06-01]
OMIM:618806	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant		HP:0001047	PMID:31447097	PCS	HP:0003593	3/25			P	HPO:probinson[2020-06-01]
OMIM:618806	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant		HP:0002788	PMID:31447097	PCS	HP:0003593				P	HPO:probinson[2020-06-01]
OMIM:618806	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant		HP:0002090	PMID:31447097	PCS	HP:0003593	5/25			P	HPO:probinson[2020-06-01]
OMIM:618806	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant		HP:0008404	PMID:31447097	PCS	HP:0003593	10/25			P	HPO:probinson[2020-06-01];HPO:probinson[2020-06-01]
OMIM:618806	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant		HP:0031545	PMID:31447097	PCS	HP:0003577	21/21			P	HPO:probinson[2020-06-01];HPO:probinson[2020-06-01]
OMIM:618806	T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant		HP:0000006	PMID:31447097	PCS					I	HPO:probinson[2020-06-01];HPO:probinson[2020-06-01]
OMIM:610282	Retinitis pigmentosa 35		HP:0000662	PMID:16199541	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-09]
OMIM:610282	Retinitis pigmentosa 35		HP:0000618	PMID:16199541	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-09]
OMIM:610282	Retinitis pigmentosa 35		HP:0000007	PMID:16199541	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-09]
OMIM:610282	Retinitis pigmentosa 35		HP:0007663	PMID:16199541	PCS					P	HPO:probinson[2023-04-09]
OMIM:610282	Retinitis pigmentosa 35		HP:0000510	PMID:16199541	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-04-09]
OMIM:300514	Fanconi anemia, complementation group B		HP:0002188	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0002101	PMID:21910217	PCS		HP:0040283			P	HPO:probinson[2018-03-07]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001195	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0003593	PMID:15502827	PCS		1/4			C	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000815	PMID:21910217	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001629	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0011463	PMID:15502827	PCS		3/4			C	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000238	PMID:21910217	PCS		2/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0002119	PMID:21910217	PCS		6/6			P	HPO:probinson[2018-03-07];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001522	PMID:21910217	PCS		2/6			C	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001643	PMID:21910217	PCS		2/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0007766	PMID:21910217	PCS		2/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0004977	PMID:21910217	PCS		5/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000135	PMID:15502827	PCS		4/4			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0003468	PMID:21910217	PCS					P	HPO:probinson[2018-03-07]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001249	PMID:15502827	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0002575	PMID:21910217	PCS		1/6			P	HPO:probinson[2018-03-07];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000396	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000054	PMID:21910217	PCS		2/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0002079	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001321	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0003220	PMID:21910217	PCS		3/3			P	HPO:probinson[2018-03-07];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0002032	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000470	PMID:21910217	PCS		2/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001680	PMID:21910217	PCS		1/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001915	PMID:21910217;PMID:15502827	PCS		5/10			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001419	PMID:21910217	PCS					I	HPO:probinson[2018-03-07]
OMIM:300514	Fanconi anemia, complementation group B		HP:0009777	PMID:21910217	PCS		5/6			P	HPO:probinson[2018-03-07];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001511	PMID:21910217	PCS	HP:0011461	4/4			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001510	PMID:21910217;PMID:15502827	PCS		6/6			P	HPO:probinson[2021-02-25];HPO:probinson[2018-03-07];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0001873	PMID:21910217;PMID:15502827	PCS		5/10			P	HPO:probinson[2021-02-25];HPO:skoehler[2018-10-08];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000369	PMID:21910217	PCS		3/6			P	HPO:probinson[2018-03-07];HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0002247	PMID:21910217	PCS		2/6			P	HPO:probinson[2021-02-25]
OMIM:300514	Fanconi anemia, complementation group B		HP:0000104	PMID:21910217	PCS		3/6			P	HPO:probinson[2018-03-07];HPO:probinson[2021-02-25]
OMIM:204000	Leber congenital amaurosis, type I		HP:0001099	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000563	PMID:16505055	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0003354	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000662	PMID:16505055	PCS		1/5			P	HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0001483	PMID:16505055	PCS	HP:0003593	2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000580	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0003296	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0002240	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0003593	PMID:16505055	PCS		6/6			C	HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0012426	PMID:16505055	PCS		1/6			P	HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000639	PMID:16505055	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000518	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000407	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000618	PMID:16505055	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000613	PMID:16505055	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0007663	PMID:16505055	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000007	OMIM:204000	IEA					I	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0001510	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0007843	PMID:16505055	PCS		2/6			P	HPO:probinson[2022-03-10]
OMIM:204000	Leber congenital amaurosis, type I		HP:0001249	OMIM:204000	IEA					P	HPO:iea[2009-02-17]
OMIM:204000	Leber congenital amaurosis, type I		HP:0000654	PMID:16505055	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0003774	PMID:23687361	PCS	HP:0003581	5/13			P	HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0003621	PMID:23687361	PCS		3/11			C	HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0003596	PMID:23687361	PCS		1/11			C	HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0000083	PMID:23687361	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0003584	PMID:23687361	PCS		1/11			C	HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0011462	PMID:23687361	PCS		6/11			C	HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0000097	PMID:23687361	PCS		5/8			P	HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0000007	PMID:23687361	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0000093	PMID:23687361	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-07]
OMIM:256020	Focal segmental glomerulosclerosis 10		HP:0012579	PMID:23687361	PCS		2/8			P	HPO:probinson[2021-07-07]
OMIM:249100	Familial Mediterranean fever, AR		HP:0003774	PMID:30171907	PCS		6/115			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002102	PMID:30171907	PCS		54/115		HP:0031796	P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002586	PMID:3306755	PCS		164/175		HP:0031796	P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002202	PMID:31941537	PCS					P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001055	PMID:30171907	PCS		13/115			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0000100	PMID:12908875	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0003593	PMID:31941537	PCS					C	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002240	OMIM:249100	IEA					P	HPO:iea[2009-02-17]
OMIM:249100	Familial Mediterranean fever, AR		HP:0011897	PMID:31941537	PCS				HP:0031796	P	HPO:probinson[2020-09-28];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0011463	PMID:31941537	PCS					C	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0011462	PMID:31941537	PCS					C	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0033332	PMID:31941537	PCS					P	HPO:probinson[2020-12-07]
OMIM:249100	Familial Mediterranean fever, AR		HP:0012450	PMID:22705602	PCS		16/446			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001701	PMID:31941537	PCS				HP:0031796	P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0100749	PMID:31205631	PCS		125/373			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002315	PMID:31941537	PCS				HP:0031796	P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001744	PMID:30171907	PCS		5/115			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0003326	PMID:31941537	PCS				HP:0031796	P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001369	PMID:30171907;PMID:22705602	PCS		218/561		HP:0031796	P	HPO:probinson[2020-09-28];HPO:skoehler[2010-06-20];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001287	OMIM:249100	IEA					P	HPO:iea[2009-02-17]
OMIM:249100	Familial Mediterranean fever, AR		HP:0003565	PMID:31941537	PCS				HP:0031796	P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002014	PMID:22705602	PCS		30/446			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0003621	PMID:31941537	PCS					C	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002013	PMID:22705602	PCS		34/446			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002574	PMID:30171907;PMID:31205631	PCS		349/488			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0100280	PMID:30171907	PCS		6/115			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0011227	PMID:31941537	PCS				HP:0031796	P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0100796	PMID:3382109	PCS			MALE	HP:0031796	P	HPO:skoehler[2019-09-07];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0100796	PMID:31205631	PCS		11/373			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002829	PMID:31941537;PMID:31205631	PCS		218/383		HP:0031796	P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0011034	PMID:30171907	PCS		5/115			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001917	PMID:22705602	PCS		17/446			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0032154	PMID:31205631	PCS		89/373			P	HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001954	PMID:31205631;PMID:22705602	PCS		520/819			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0000007	PMID:31941537	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0002027	PMID:22705602	PCS		353/446		HP:0031796	P	HPO:iea[2009-02-17];HPO:probinson[2020-09-28]
OMIM:249100	Familial Mediterranean fever, AR		HP:0001974	PMID:31941537	PCS				HP:0031796	P	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-28]
OMIM:613953	Immunodeficiency 51		HP:0033605	PMID:27930337	PCS		9/21			P	HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0004332	PMID:21350122	PCS		0/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0031409	PMID:21350122	PCS		0/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0200039	PMID:21350122	PCS		1/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0001581	PMID:21350122	PCS		1/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0002090	PMID:27930337	PCS		5/21			P	HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0025084	PMID:21350122;PMID:27930337	PCS		12/22			P	HPO:probinson[2021-05-30];HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0011108	PMID:21350122;PMID:27930337	PCS		5/22			P	HPO:probinson[2021-05-30];HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0011370	PMID:21350122	PCS		1/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0031292	PMID:21350122	PCS		1/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0009098	PMID:27930337	PCS		20/21			P	HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0002728	PMID:21350122	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0011132	PMID:21350122;PMID:27930337	PCS		8/22			P	HPO:probinson[2021-05-30];HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0002726	PMID:21350122	PCS		1/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0000007	PMID:21350122	PCS					I	HPO:probinson[2013-08-10]
OMIM:613953	Immunodeficiency 51		HP:0000403	PMID:21350122	PCS		1/1			P	HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0002837	PMID:21350122;PMID:27930337	PCS		3/22			P	HPO:probinson[2021-05-30];HPO:lccarmody[2018-10-04];HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0000964	PMID:27930337	PCS		4/21			P	HPO:probinson[2021-05-30]
OMIM:613953	Immunodeficiency 51		HP:0002205	OMIM:613953	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000286	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000486	PMID:26111154	PCS					P	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0001290	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000739	PMID:26111154	PCS					P	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0001845	OMIM:616803	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000678	PMID:26111154	PCS					P	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000414	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0100807	OMIM:616803	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0001847	OMIM:616803	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0030084	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0001763	OMIM:616803	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000358	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0001249	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000494	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0002650	PMID:26111154	PCS					P	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000431	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000750	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000194	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0001263	PMID:26111154	PCS					P	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0005280	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000648	PMID:26111154	PCS					P	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000768	PMID:26111154	PCS					P	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0002007	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000006	PMID:26111154	PCS					I	HPO:probinson[2017-06-17]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000369	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000545	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0008428	OMIM:616803	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616803	Lamb-Shaffer syndrome		HP:0000324	OMIM:616803	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609923	Retinitis pigmentosa 31		HP:0001123	PMID:17924349	PCS		HP:0040282			P	HPO:probinson[2013-03-31]
OMIM:609923	Retinitis pigmentosa 31		HP:0000510	OMIM:609923	TAS					P	HPO:skoehler[2015-01-27]
OMIM:609923	Retinitis pigmentosa 31		HP:0007722	PMID:17924349	PCS					P	HPO:probinson[2013-03-31]
OMIM:609923	Retinitis pigmentosa 31		HP:0007843	PMID:17924349	PCS					P	HPO:probinson[2013-03-31]
OMIM:609923	Retinitis pigmentosa 31		HP:0000006	PMID:17924349	PCS					I	HPO:probinson[2013-01-09]
OMIM:609923	Retinitis pigmentosa 31		HP:0000512	PMID:17924349	PCS		HP:0040282			P	HPO:probinson[2013-03-31]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001771	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0010804	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0005257	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001371	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003273	PMID:26700687	PCS		3/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001252	PMID:26700687	PCS		5/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003196	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003391	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000678	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000278	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003306	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003700	PMID:26700687	PCS		4/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000494	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002474	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001541	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003121	PMID:26700687	PCS		3/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003044	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000490	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002352	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0033454	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0008081	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0034198	PMID:26700687	PCS		5/10			C	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000602	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000767	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000007	PMID:26700687	PCS					I	HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000207	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002987	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000520	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000322	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000883	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002943	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000369	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001612	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003577	PMID:26700687	PCS		1/10			C	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002202	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002089	PMID:26700687	PCS		5/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0030674	PMID:26700687	PCS		4/10			C	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003691	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002240	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001790	PMID:26700687	PCS		4/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003690	PMID:26700687	PCS		4/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001270	PMID:26700687	PCS		4/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0030319	PMID:26700687	PCS		4/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0009004	PMID:26700687	PCS		6/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002515	PMID:26700687	PCS		2/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000218	PMID:26700687	PCS		4/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003327	PMID:26700687	PCS		3/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002359	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001623	PMID:26700687	PCS		3/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001561	PMID:26700687	PCS		7/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002650	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001883	PMID:26700687	PCS		6/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0011309	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000431	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000276	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002098	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0003100	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000470	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0001558	PMID:26700687	PCS		7/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0002007	PMID:26700687	PCS		3/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000664	PMID:26700687	PCS		1/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:620369	Congenital myopathy 22B, severe fetal		HP:0000347	PMID:26700687	PCS		3/10			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0200150	OMIM:614972	TAS					P	HPO:skoehler[2013-06-13]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0200148	OMIM:614972	TAS					P	HPO:skoehler[2013-06-13]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0000007	OMIM:614972	TAS		HP:0040283			I	HPO:skoehler[2012-12-30]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0000989	OMIM:614972	TAS					P	HPO:skoehler[2013-01-21]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0001406	OMIM:614972	TAS					P	HPO:skoehler[2013-01-21]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0025116	OMIM:614972	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0000006	OMIM:614972	TAS					I	HPO:skoehler[2012-12-30]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0000952	OMIM:614972	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:614972	Cholestasis, intrahepatic, of pregnancy 3		HP:0001622	OMIM:614972	TAS					P	HPO:skoehler[2012-12-30]
OMIM:500001	Leber optic atrophy and dystonia		HP:0000572	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0003202	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0002015	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0002067	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0002650	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0000496	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0001112	OMIM:500001	TAS					P	HPO:probinson[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0001332	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0001260	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0002151	OMIM:500001	TAS					P	HPO:probinson[2012-07-22]
OMIM:500001	Leber optic atrophy and dystonia		HP:0002493	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0002490	OMIM:500001	TAS					P	HPO:probinson[2012-07-22]
OMIM:500001	Leber optic atrophy and dystonia		HP:0000726	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0001427	OMIM:500001	IEA					I	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0009830	OMIM:500001	IEA					P	HPO:skoehler[2010-06-20]
OMIM:500001	Leber optic atrophy and dystonia		HP:0000648	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0001257	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0002305	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:500001	Leber optic atrophy and dystonia		HP:0001249	OMIM:500001	IEA					P	HPO:iea[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0002267	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0002421	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0001276	OMIM:272800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272800	Tay-Sachs disease		HP:0000980	OMIM:272800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272800	Tay-Sachs disease		HP:0001250	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0003495	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0001252	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0002361	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0003593	OMIM:272800	TAS					C	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0010729	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0001290	OMIM:272800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272800	Tay-Sachs disease		HP:0000726	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0000618	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0000007	OMIM:272800	TAS					I	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0002835	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:272800	Tay-Sachs disease		HP:0000741	OMIM:272800	TAS					P	HPO:probinson[2009-02-17]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0002421	OMIM:618184	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0003577	PMID:12953275	PCS		1/1			C	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0003431	PMID:8816708	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0002540	OMIM:618184	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0003693	PMID:10319895	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001252	PMID:10319895;PMID:12953275	PCS		2/2			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0006829	OMIM:618184	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0003593	PMID:8816708;PMID:10319895	PCS		2/2			C	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001270	PMID:8816708;PMID:10319895;PMID:12953275	PCS		3/3			P	HPO:probinson[2022-08-18];HPO:skoehler[2019-02-15];HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001349	PMID:12953275	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001324	PMID:10319895	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001763	PMID:10319895	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001265	PMID:10319895	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0003202	OMIM:618184	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0002375	OMIM:618184	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0002650	PMID:10319895	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0031936	PMID:12953275	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0025335	PMID:12953275	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0003383	PMID:10319895;PMID:12953275	PCS		2/2			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001284	PMID:12953275	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0003380	PMID:10319895	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0010871	PMID:10319895	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0032988	PMID:12953275	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0001558	OMIM:618184	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0002747	OMIM:618184	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618184	Neuropathy, congenital hypomyelinating, 2		HP:0000006	PMID:8816708	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-18]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001397	PMID:9399886	PCS		1/1			P	HPO:probinson[2021-07-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001254	PMID:9399886	PCS		1/1			P	HPO:skoehler[2014-03-24];HPO:probinson[2021-07-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0003236	OMIM:212138	TAS					P	HPO:skoehler[2014-03-24]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001695	PMID:9399886	PCS		1/1			P	HPO:probinson[2021-07-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001250	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:6000575	PMID:3297709	PCS		6/6			P	HPO:probinson[2024-04-03]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001252	OMIM:212138	TAS					P	HPO:skoehler[2014-11-26]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0002240	PMID:9399886	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:6000574	PMID:9323572	PCS		6/6			P	HPO:probinson[2024-04-03]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001290	OMIM:212138	TAS					P	HPO:skoehler[2017-07-13]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0000737	OMIM:212138	TAS					P	HPO:skoehler[2014-03-24]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001987	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001943	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0002615	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001324	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0002910	OMIM:212138	TAS					P	HPO:skoehler[2014-03-24]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0004756	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001662	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0003201	OMIM:212138	TAS					P	HPO:skoehler[2014-03-24]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0006682	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0000007	PMID:9399886	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001998	PMID:9399886	PCS		1/1			P	HPO:probinson[2021-07-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001638	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0006543	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001714	OMIM:212138	PCS				HP:0012825	P	HPO:probinson[2012-04-08]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001678	OMIM:212138	IEA					P	HPO:iea[2009-02-17]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0003215	OMIM:212138	TAS					P	HPO:skoehler[2014-03-24]
OMIM:212138	Carnitine-acylcarnitine translocase deficiency		HP:0001259	OMIM:212138	TAS					P	HPO:skoehler[2014-03-24]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002025	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000286	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002023	PMID:17334363	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001212	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000486	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0004322	PMID:17334363	PCS	HP:0003593	2/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002021	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001250	PMID:17334363	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0010609	OMIM:305450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001252	PMID:17334363	PCS		9/10			P	HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0004482	PMID:17334363	PCS		7/9			P	HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001171	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0005490	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0011266	PMID:17334363	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0010055	PMID:17334363	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0011220	PMID:17334363	PCS		9/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002938	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000316	PMID:17334363	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000954	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000678	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000238	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0009466	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002019	PMID:17334363	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001249	PMID:17334363	PCS		9/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0020206	PMID:17334363	PCS		7/7			P	HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000175	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000494	PMID:17334363	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000453	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001263	OMIM:305450	TAS					P	HPO:skoehler[2014-04-04]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0012385	OMIM:305450	TAS					P	HPO:skoehler[2013-10-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000407	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001419	PMID:17334363	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002828	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000448	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001537	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001338	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000047	PMID:17334363	PCS		0/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000960	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001257	PMID:17334363	PCS		2/4			P	HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000204	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001476	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000343	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000189	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000023	PMID:17334363	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000260	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002282	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001270	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0008070	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0009762	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001627	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0030084	OMIM:305450	TAS					P	HPO:skoehler[2014-09-21]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001620	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000179	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002236	PMID:17334363	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001545	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000154	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002213	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000470	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0011304	PMID:17334363	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0009473	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001319	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002007	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001357	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0001159	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0007018	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000028	PMID:17334363	PCS		4/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0002566	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:305450	Opitz-Kaveggia syndrome		HP:0000347	OMIM:305450	IEA					P	HPO:iea[2009-02-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000286	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000365	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0004322	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000089	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002365	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001250	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002066	PMID:26307080	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000160	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0012448	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0008070	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001988	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0030186	PMID:26307080	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0003307	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002714	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001620	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0200021	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001249	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0003468	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000677	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001348	PMID:26307080	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002751	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000252	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000494	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002213	OMIM:616817	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002078	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002079	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0002750	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000293	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001260	PMID:26307080	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000592	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0004570	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001518	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000407	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000767	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000007	PMID:26159176	PCS					I	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000821	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000601	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000823	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001511	OMIM:616817	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000400	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001510	PMID:26159176	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001257	PMID:26307080	PCS					P	HPO:probinson[2017-06-17]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0001015	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000028	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616817	Microcephaly, short stature, and impaired glucose metabolism 2		HP:0000347	OMIM:616817	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0007417	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002740	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002840	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002741	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002240	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0100523	PMID:18422995	PCS					P	HPO:probinson[2017-09-04]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002716	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002955	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0006532	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003206	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0005406	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0001744	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002754	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003621	OMIM:233690	IEA					C	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003203	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0005224	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0100658	OMIM:233690	TAS					P	HPO:probinson[2017-09-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002726	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0000007	OMIM:233690	IEA					I	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0000964	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002724	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003514	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002723	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002742	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002842	OMIM:233690	IEA					P	HPO:iea[2009-02-17]
OMIM:233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002721	OMIM:233690	IEA					P	HPO:skoehler[2018-10-08]
OMIM:183100	Spinocerebellar atrophy with pupillary paralysis		HP:0007263	OMIM:183100	IEA					P	HPO:iea[2009-02-17]
OMIM:183100	Spinocerebellar atrophy with pupillary paralysis		HP:0000006	OMIM:183100	IEA					I	HPO:iea[2009-02-17]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0007814	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0010804	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0002188	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0025444	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0003593	PMID:34186028	PCS		1/2			C	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0032794	PMID:34186028	PCS	HP:0003593	2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0010862	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0033725	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0000639	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0000711	PMID:34186028	PCS		1/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0000219	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0025517	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0003623	PMID:34186028	PCS		1/2			C	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0000252	PMID:34186028	PCS		4/4			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0006956	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0001344	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0031936	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0011968	PMID:34186028	PCS		1/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0001263	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0002194	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0100321	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0012520	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0003819	PMID:34186028	PCS		1/2			C	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0032792	PMID:34186028	PCS	HP:0003593	2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0000729	PMID:34186028	PCS		1/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0025405	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0000007	PMID:34186028	PCS					I	HPO:probinson[2021-10-31];HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0001338	PMID:34186028	PCS		2/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0007359	PMID:34186028	PCS	HP:0003623	1/2			P	HPO:probinson[2021-10-31]
OMIM:619517	Neurodevelopmental disorder with seizures and brain abnormalities		HP:0001257	PMID:34186028	PCS		1/2			P	HPO:probinson[2021-10-31]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002223	OMIM:601358	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0003037	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002465	OMIM:601358	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000200	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0004322	PMID:22822383	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001250	PMID:22366787	PCS	HP:0011463	22/35			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001250	PMID:22822383	PCS		3/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002066	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001252	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0003196	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0010049	PMID:22366787	PCS		16/32			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000957	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000319	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000718	PMID:22822383	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000998	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000954	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0100807	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002019	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0006237	PMID:22366787;PMID:22822383	PCS		29/38			P	HPO:probinson[2022-09-28];HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001249	PMID:22366787	PCS		36/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000358	PMID:22822383	PCS		2/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0003502	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0003623	PMID:22822383	PCS		3/3			C	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000494	PMID:22822383	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000252	PMID:22366787;PMID:22822383	PCS		20/38			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0007946	OMIM:601358	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001344	OMIM:601358	TAS					P	HPO:skoehler[2014-11-26]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002750	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0011968	PMID:22822383	PCS		2/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001263	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000294	PMID:22822383	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0010511	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0012810	OMIM:601358	TAS					P	HPO:skoehler[2014-06-24]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0007392	PMID:22366787	PCS		18/36			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000607	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001537	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000964	OMIM:601358	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002705	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000527	PMID:22822383	PCS		2/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002307	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0025325	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000400	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001852	PMID:22822383	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000289	PMID:22366787	PCS		31/36			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000006	PMID:22366787	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000446	PMID:22822383	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000325	PMID:22822383	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000687	OMIM:601358	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000384	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000343	PMID:22366787;PMID:22822383	PCS		30/39			P	HPO:probinson[2022-09-28];HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000463	PMID:22366787;PMID:22822383	PCS		33/39			P	HPO:probinson[2022-09-28];HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001156	OMIM:601358	IEA					P	HPO:iea[2009-02-17]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000023	PMID:22822383	PCS		2/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002162	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0008070	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0011359	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0010864	PMID:22366787;PMID:22822383	PCS		25/39			P	HPO:probinson[2022-09-28];HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0010743	PMID:22366787	PCS		16/32			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001508	PMID:22822383	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000414	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001822	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000736	PMID:22822383	PCS		2/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000219	PMID:22366787;PMID:22822383	PCS		29/39			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0009765	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000179	PMID:22366787	PCS		32/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0009803	OMIM:601358	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000154	PMID:22366787	PCS		34/36			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002650	OMIM:601358	TAS					P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000232	OMIM:601358	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001680	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0045025	OMIM:601358	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0100040	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0100678	PMID:22822383	PCS		2/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0008064	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002209	PMID:22366787;PMID:22822383	PCS		36/39			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001511	PMID:22366787	PCS		10/34			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0002205	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0007018	PMID:22822383	PCS		1/3			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0001510	PMID:22366787	PCS		19/36			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0009836	PMID:22366787	PCS		21/35			P	HPO:probinson[2022-09-28]
OMIM:601358	Nicolaides-Baraitser syndrome		HP:0000028	PMID:22822383	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:107200	Anosmia, congenital		HP:0000458	OMIM:107200	TAS	HP:0003577				P	HPO:skoehler[2009-02-17]
OMIM:107200	Anosmia, congenital		HP:0000006	OMIM:107200	IEA					I	HPO:iea[2009-02-17]
OMIM:188055	Thrombophilia due to deficiency of activated protein C cofactor		HP:0003581	OMIM:188055	TAS					C	HPO:probinson[2012-07-22]
OMIM:188055	Thrombophilia due to deficiency of activated protein C cofactor		HP:0100602	OMIM:188055	TAS					H	HPO:probinson[2013-02-24]
OMIM:188055	Thrombophilia due to deficiency of activated protein C cofactor		HP:0012175	OMIM:188055	TAS					P	HPO:probinson[2013-02-24]
OMIM:188055	Thrombophilia due to deficiency of activated protein C cofactor		HP:0100724	OMIM:188055	IEA					P	HPO:skoehler[2015-01-27]
OMIM:188055	Thrombophilia due to deficiency of activated protein C cofactor		HP:0002625	OMIM:188055	TAS					P	HPO:probinson[2009-02-17]
OMIM:188055	Thrombophilia due to deficiency of activated protein C cofactor		HP:0000006	OMIM:188055	TAS					I	HPO:probinson[2009-02-17]
OMIM:188055	Thrombophilia due to deficiency of activated protein C cofactor		HP:0003645	OMIM:188055	TAS					P	HPO:probinson[2009-02-17]
OMIM:614033	Glyoxalase II deficiency		HP:0003258	PMID:5485124	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-20]
OMIM:614033	Glyoxalase II deficiency		HP:0000006	PMID:5485124	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0001892	PMID:18065693;PMID:23253071;PMID:20081061;PMID:19336737	PCS		10/15			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0000132	PMID:20081061	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0011870	PMID:20081061;PMID:19336737	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0011871	PMID:20081061;PMID:19336737	PCS		0/2			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20];HPO:probinson[2024-03-16]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0008320	PMID:23253071;PMID:20081061	PCS		5/5			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0011877	PMID:18065693;PMID:19336737	PCS		8/8			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0008148	PMID:20081061;PMID:19336737	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0001873	PMID:18065693;PMID:23253071;PMID:20081061;PMID:19336737	PCS		15/15			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0000006	PMID:18065693	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0004866	PMID:23253071;PMID:20081061;PMID:19336737	PCS		6/6			P	HPO:probinson[2021-06-20]
OMIM:619271	Bleeding disorder, platelet-type, 24, autosomal dominant		HP:0032438	PMID:18065693;PMID:23253071;PMID:20081061;PMID:19336737	PCS		15/15			P	HPO:probinson[2021-06-20]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001276	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002169	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001332	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001250	PMID:27696117	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0012707	PMID:27696117	PCS		1/1			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001252	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001290	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0040213	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0000518	PMID:27696117	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001508	PMID:27696117	PCS		5/5			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002878	PMID:27696117	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002119	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001522	PMID:27696117	PCS		4/5			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001643	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0000952	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0003623	PMID:27696117	PCS		5/5			C	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0005943	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002059	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002015	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0003344	PMID:27696117	PCS		5/5			P	HPO:probinson[2022-10-12];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001662	PMID:27696117	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002079	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0011968	PMID:27696117	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002033	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002151	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0005484	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002490	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0000407	OMIM:617248	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0000007	PMID:27696117	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001998	PMID:27696117	PCS		1/5			P	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0003811	PMID:27696117	PCS		1/5			C	HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001510	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0002104	PMID:27696117	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001337	PMID:27696117	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0003535	PMID:27696117	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-12]
OMIM:617248	3-methylglutaconic aciduria, type VIII		HP:0001875	OMIM:617248	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0000286	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001298	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0000253	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2013-01-22]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0003577	OMIM:614741	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001583	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0000343	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0003542	OMIM:614741	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001992	OMIM:614741	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001250	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0002098	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0002151	OMIM:614741	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001263	OMIM:614741	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001252	OMIM:614741	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0002240	OMIM:614741	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001290	OMIM:614741	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0003828	OMIM:614741	TAS					M	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0009830	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0000007	OMIM:614741	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0001943	OMIM:614741	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0000219	OMIM:614741	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614741	Mitochondrial pyruvate carrier deficiency		HP:0003128	OMIM:614741	TAS					P	HPO:skoehler[2012-10-17]
OMIM:230400	Galactosemia		HP:0002069	PMID:25681079	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:230400	Galactosemia		HP:0008209	OMIM:230400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:230400	Galactosemia		HP:0001410	OMIM:230400	IEA					P	HPO:iea[2009-02-17]
OMIM:230400	Galactosemia		HP:0003355	OMIM:230400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:230400	Galactosemia		HP:0001394	OMIM:230400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:230400	Galactosemia		HP:0002240	OMIM:230400	IEA					P	HPO:iea[2009-02-17]
OMIM:230400	Galactosemia		HP:0001290	PMID:25681079	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:230400	Galactosemia		HP:0031964	PMID:35028268	PCS		1/2			P	HPO:probinson[2022-04-30]
OMIM:230400	Galactosemia		HP:0000518	PMID:35028268	PCS	HP:0003593	1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:230400	Galactosemia		HP:0001508	OMIM:230400	IEA					P	HPO:iea[2009-02-17]
OMIM:230400	Galactosemia		HP:0000815	OMIM:230400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:230400	Galactosemia		HP:0012592	OMIM:230400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:230400	Galactosemia		HP:0004918	OMIM:230400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:230400	Galactosemia		HP:4000208	PMID:25681079	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:230400	Galactosemia		HP:0001249	OMIM:230400	IEA					P	HPO:iea[2009-02-17]
OMIM:230400	Galactosemia		HP:0000952	PMID:25681079	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:230400	Galactosemia		HP:0001942	OMIM:230400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:230400	Galactosemia		HP:0003623	PMID:25681079	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:230400	Galactosemia		HP:0002014	OMIM:230400	IEA					P	HPO:iea[2009-02-17]
OMIM:230400	Galactosemia		HP:0031956	PMID:35028268	PCS		1/2			P	HPO:probinson[2022-04-30]
OMIM:230400	Galactosemia		HP:0000750	PMID:25681079	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:230400	Galactosemia		HP:0002013	PMID:25681079	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:230400	Galactosemia		HP:0011968	PMID:25681079	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:230400	Galactosemia		HP:0410064	PMID:14680973	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:230400	Galactosemia		HP:0410062	PMID:11092512	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:230400	Galactosemia		HP:0410063	PMID:14680973	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:230400	Galactosemia		HP:0410061	PMID:11092512;PMID:7671965	PCS		20/20			P	HPO:NicoleVasilevsky[2018-02-23];HPO:NicoleVasilevsky[2018-03-02]
OMIM:230400	Galactosemia		HP:0012023	OMIM:230400	TAS					P	HPO:skoehler[2012-07-27]
OMIM:230400	Galactosemia		HP:0012024	PMID:35028268;PMID:25681079	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-28];HPO:skoehler[2009-02-17];HPO:probinson[2022-04-30]
OMIM:230400	Galactosemia		HP:0001878	OMIM:230400	IEA					P	HPO:iea[2009-02-17]
OMIM:230400	Galactosemia		HP:0000007	PMID:25681079	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-06-28]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000365	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0004322	PMID:18252230	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001596	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002164	PMID:18252230	PCS		10/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002043	PMID:21477109	PCS		1/2			P	HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001251	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0012227	PMID:18252230	PCS		1/12			P	HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0045051	PMID:18252230	PCS		4/12			P	HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000939	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000958	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0011463	PMID:21477109;PMID:18252230	PCS		6/14			C	HPO:probinson[2024-02-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001903	PMID:21477109	PCS		1/2			P	HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0011462	PMID:18252230	PCS		4/12			C	HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000938	PMID:21477109	PCS		1/2			P	HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0006530	PMID:21477109	PCS		1/2			P	HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002216	PMID:18252230	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0005528	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002239	PMID:21477109	PCS		1/2			P	HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002514	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0007427	PMID:18252230	PCS		9/12			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0009926	PMID:21477109;PMID:18252230	PCS		7/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06];HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000252	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0003621	PMID:18252230	PCS		4/12			C	HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002213	OMIM:613990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0005743	PMID:18252230	PCS		2/12			P	HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000750	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001882	PMID:21477109	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001321	PMID:18252230	PCS		1/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0031413	PMID:21477109;PMID:18252230	PCS		11/12			P	HPO:probinson[2024-02-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001915	PMID:18252230	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0008661	PMID:18252230	PCS		1/12			P	HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0008404	PMID:21477109	PCS		2/2			P	HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001511	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001873	PMID:21477109;PMID:18252230	PCS		11/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06];HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002206	PMID:18252230	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0002745	PMID:21477109;PMID:18252230	PCS		10/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06];HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001972	PMID:21477109	PCS		2/2			P	HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001510	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0007898	PMID:18252230	PCS		1/12			P	HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001876	PMID:21477109	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-02-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000028	OMIM:613990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0000006	PMID:18252230	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613990	Dyskeratosis congenita, autosomal dominant 3		HP:0001875	PMID:21477109	PCS		2/2			P	HPO:probinson[2024-02-17]
OMIM:279000	Young syndrome		HP:0005425	OMIM:279000	IEA					P	HPO:iea[2009-02-17]
OMIM:279000	Young syndrome		HP:0010959	OMIM:279000	IEA					P	HPO:iea[2009-02-17]
OMIM:279000	Young syndrome		HP:0002110	OMIM:279000	IEA					P	HPO:iea[2009-02-17]
OMIM:279000	Young syndrome		HP:0000007	OMIM:279000	IEA					I	HPO:iea[2009-02-17]
OMIM:279000	Young syndrome		HP:0002837	OMIM:279000	IEA					P	HPO:iea[2009-02-17]
OMIM:279000	Young syndrome		HP:0000027	OMIM:279000	IEA					P	HPO:iea[2009-02-17]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0003621	PMID:11369620	PCS		1/4			C	HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0003596	PMID:11369620	PCS		1/4			C	HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0003641	PMID:11369620	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:6000240	PMID:11369620;PMID:4372252	PCS		14/14			P	HPO:probinson[2024-02-09];HPO:probinson[2024-02-09];HPO:probinson[2024-04-03]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0011463	PMID:11369620	PCS		1/4			C	HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0002904	PMID:11369620	PCS		3/3			P	HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0001878	PMID:11369620	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0000007	PMID:11369620	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0001923	PMID:11369620	PCS		3/3			P	HPO:probinson[2024-02-09]
OMIM:266120	Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemiadue to		HP:0003623	PMID:11369620	PCS		1/4			C	HPO:probinson[2024-02-09]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002069	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000242	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000486	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000160	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0045075	OMIM:234100	TAS					P	HPO:probinson[2022-05-07]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000518	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000958	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000639	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001009	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0003508	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0003307	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002779	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000752	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002414	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0003745	OMIM:234100	IEA					I	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001249	OMIM:234100	IEA		15%			P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000494	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000252	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0004334	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000695	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002870	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001266	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001382	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000767	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000689	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002705	OMIM:234100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000568	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000883	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000248	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000567	OMIM:234100	TAS					P	HPO:probinson[2015-07-19]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000369	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001155	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0030799	OMIM:234100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:234100	Hallermann-Streiff syndrome		HP:0003016	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000189	OMIM:234100	TAS					P	HPO:skoehler[2013-08-18]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000460	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001592	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0008070	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001547	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000612	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000218	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0006532	OMIM:234100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000653	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0006611	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002213	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002650	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0010539	OMIM:234100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000233	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000232	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000430	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0003100	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000592	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000272	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002691	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002092	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0011069	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0001518	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000822	OMIM:234100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000426	PMID:15347328	PCS					P	HPO:lccarmody[2018-09-24]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002209	OMIM:234100	TAS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000268	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002007	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002205	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0002645	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000028	OMIM:234100	IEA					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000347	OMIM:234100	PCS					P	HPO:probinson[2009-02-17]
OMIM:234100	Hallermann-Streiff syndrome		HP:0000588	OMIM:234100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0008194	PMID:29339498	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0003621	PMID:29339498	PCS		1/24			C	HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0003596	PMID:29339498	PCS		11/24			C	HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0000825	PMID:29339498	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0003584	PMID:29339498	PCS		2/24			C	HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0001087	PMID:29339498	PCS		4/24			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0011462	PMID:29339498	PCS		10/24			C	HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0000519	PMID:29339498	PCS		4/24			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0012197	PMID:29339498	PCS		10/24			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0040270	PMID:29339498	PCS		2/24			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0005978	PMID:29339498	PCS		15/24			P	HPO:probinson[2022-09-06]
OMIM:147630	Insulinomatosis and diabetes mellitus		HP:0000006	PMID:29339498	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0003477	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000122	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002384	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002140	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0003196	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0003593	PMID:33971351	PCS		1/1			C	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001290	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0012506	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000637	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0003763	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0007429	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001187	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0005301	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000012	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000490	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002033	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001182	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0008081	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002829	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000403	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000527	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0003758	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002944	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0004209	PMID:34183358	PCS		3/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000400	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000125	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000248	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000369	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000006	PMID:31698099	PCS					I	HPO:probinson[2022-09-04]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0006349	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001397	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002003	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000341	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001396	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000582	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002002	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0011914	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000185	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001791	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0005990	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0004383	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0010783	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0010943	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002917	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0012172	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0012450	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0006297	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001669	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000219	PMID:31698099;PMID:34183358	PCS		2/13			P	HPO:probinson[2021-09-05];HPO:probinson[2021-09-05];HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002119	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000218	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0006610	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000973	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000577	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001562	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0025352	PMID:31698099	PCS					I	HPO:probinson[2021-09-05];HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002136	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002015	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001682	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001047	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000750	PMID:34183358	PCS		5/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0006837	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001041	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002099	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0010819	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000592	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0011228	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0011623	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0100710	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0008064	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0032152	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000506	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001719	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0040288	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002804	PMID:31698099	PCS	HP:0011461	1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001558	PMID:33971351	PCS	HP:0011461	1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001558	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000348	PMID:34183358	PCS		3/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000744	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002527	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002007	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001433	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000347	PMID:31698099;PMID:34183358	PCS		4/13			P	HPO:probinson[2021-09-05];HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002643	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002188	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000684	PMID:34183358;PMID:33971351	PCS		2/13			P	HPO:probinson[2021-09-05];HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001371	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001250	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000160	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0003273	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001252	PMID:31698099;PMID:34183358	PCS		7/13			P	HPO:probinson[2021-09-05];HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0030891	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0012304	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000958	PMID:34183358	PCS		6/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001409	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0011342	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0009027	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000954	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000678	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0031909	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0003307	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001007	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001249	PMID:34183358	PCS		12/23			P	HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001386	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0006659	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000054	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002353	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000574	PMID:31698099;PMID:34183358	PCS		2/13			P	HPO:probinson[2021-09-05];HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001025	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0011968	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000293	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001382	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001263	PMID:31698099;PMID:34183358;PMID:33971351	PCS		18/25			P	HPO:probinson[2021-09-05];HPO:probinson[2021-10-31];HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0009890	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0006380	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000729	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0040189	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000448	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000601	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002901	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002987	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000960	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002104	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000540	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000023	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0010747	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001195	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0004220	PMID:31698099	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002040	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0005272	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001508	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0012095	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001629	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0011560	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0030043	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002835	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002714	PMID:34183358	PCS		3/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002315	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000256	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001347	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002212	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000154	PMID:34183358	PCS		2/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0031935	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0005280	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0009110	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001878	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0002209	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000824	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0030051	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000389	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000268	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000664	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000028	PMID:34183358	PCS		1/12			P	HP:probinson[2021-10-31]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0000303	PMID:31698099;PMID:33971351	PCS		2/2			P	HPO:probinson[2021-09-05]
OMIM:619503	Neurodevelopmental disorder with hypotonia and dysmorphic facies		HP:0001238	PMID:33971351	PCS		1/1			P	HPO:probinson[2021-09-05]
OMIM:231050	Geleophysic dysplasia 1		HP:0001650	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0000582	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0001792	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0001773	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0000343	PMID:21415077	PCS		18/19			P	HPO:probinson[2012-05-01];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0004322	PMID:21415077	PCS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0000463	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0001250	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0100490	OMIM:231050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0003196	PMID:21415077	PCS		11/16			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0002680	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0002240	PMID:21415077	PCS		5/17			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0001072	PMID:21415077	PCS		10/15			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0010446	OMIM:231050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:231050	Geleophysic dysplasia 1		HP:0003090	OMIM:231050	TAS					P	HPO:probinson[2012-05-26]
OMIM:231050	Geleophysic dysplasia 1		HP:0000319	OMIM:231050	TAS					P	HPO:probinson[2012-05-01]
OMIM:231050	Geleophysic dysplasia 1		HP:0000938	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0000219	PMID:21415077	PCS		18/18			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0002777	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0000311	PMID:21415077	PCS		14/15			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0001620	PMID:21415077	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0000154	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0003026	PMID:21415077	PCS		15/15			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0004279	OMIM:231050	TAS					P	HPO:probinson[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0000431	PMID:21415077	PCS		14/15			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0001387	PMID:21415077	PCS		20/20			P	HPO:probinson[2012-07-29];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0002673	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0004894	PMID:21415077	PCS		6/13			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0002750	PMID:21415077	PCS		12/13			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0003300	PMID:21415077	PCS		6/10			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0000391	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0001263	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0045025	PMID:21415077	PCS		13/15			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0005041	PMID:21415077	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0002092	PMID:21415077	PCS		4/11			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0010579	PMID:21415077	PCS		5/8			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0006161	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0009473	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0100679	OMIM:231050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0001718	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0000926	PMID:21415077	PCS		5/8			P	HPO:probinson[2024-03-08]
OMIM:231050	Geleophysic dysplasia 1		HP:0000767	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0001239	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0001635	OMIM:231050	IEA					P	HPO:iea[2009-02-17]
OMIM:231050	Geleophysic dysplasia 1		HP:0000007	PMID:21415077	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:211380	Elsahy-Waters syndrome		HP:0002025	OMIM:211380	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0000684	PMID:27431290	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000486	PMID:28988429	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000485	PMID:28988429	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0001571	PMID:28988429	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000518	PMID:28988429	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000316	PMID:27431290;PMID:28988429	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0020049	PMID:28988429	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0001249	PMID:27431290	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000358	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0000494	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0003764	PMID:28988429	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0004378	PMID:27431290	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000574	PMID:28988429	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0001263	PMID:28988429	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0010554	PMID:28988429	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0011800	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0000808	OMIM:211380	IEA					P	HPO:iea[2009-02-17]
OMIM:211380	Elsahy-Waters syndrome		HP:0000327	PMID:28988429	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000767	OMIM:211380	IEA					P	HPO:iea[2009-02-17]
OMIM:211380	Elsahy-Waters syndrome		HP:0000007	OMIM:211380	IEA					I	HPO:iea[2009-02-17]
OMIM:211380	Elsahy-Waters syndrome		HP:0000689	PMID:28988429	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000048	PMID:27431290	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0008689	PMID:27431290	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000289	PMID:28988429	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000047	PMID:27431290	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000520	PMID:27431290	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000248	OMIM:211380	IEA					P	HPO:skoehler[2019-04-18]
OMIM:211380	Elsahy-Waters syndrome		HP:0004602	PMID:28988429	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000369	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0000324	OMIM:211380	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0000445	PMID:28988429	PCS		2/2			P	HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000341	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0003577	PMID:27431290	PCS		1/1			C	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000343	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0000463	PMID:27431290	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0001156	OMIM:211380	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0010862	PMID:27431290	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0011910	PMID:27431290	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000337	PMID:28988429	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000414	PMID:28988429	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000219	PMID:27431290	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000218	PMID:28988429	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0009765	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0006610	PMID:27431290	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000179	OMIM:211380	IEA					P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0001545	OMIM:211380	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:211380	Elsahy-Waters syndrome		HP:0000456	PMID:28988429	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000431	PMID:27431290	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000193	OMIM:211380	IEA					P	HPO:iea[2009-02-17]
OMIM:211380	Elsahy-Waters syndrome		HP:0000272	PMID:27431290;PMID:28988429	PCS		2/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:6000744	PMID:20949527	PCS		2/2			P	HPO:probinson[2024-06-29]
OMIM:211380	Elsahy-Waters syndrome		HP:0011069	PMID:28988429	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0012796	PMID:28988429	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0011079	PMID:28988429	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0006485	PMID:27431290	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000667	PMID:28988429	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000307	PMID:27431290	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000664	PMID:27431290;PMID:28988429	PCS		2/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000501	PMID:28988429	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-24]
OMIM:211380	Elsahy-Waters syndrome		HP:0000303	OMIM:211380;PMID:28988429	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:618635	Siddiqi syndrome		HP:0002376	PMID:28067622	PCS					P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0001761	PMID:28067622	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0031936	PMID:28067622	PCS		5/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0001371	PMID:28067622	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0001250	PMID:28067622	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0002451	PMID:28067622	PCS		3/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0001263	PMID:28067622	IEA		5/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0000020	PMID:28067622	PCS		1/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0001270	PMID:28067622	PCS		5/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0008064	PMID:28067622	PCS		5/5			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0000407	PMID:28067622	PCS	HP:0003593	5/5			P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0007210	PMID:28067622	PCS					P	HPO:probinson[2020-07-24]
OMIM:618635	Siddiqi syndrome		HP:0000007	PMID:28067622	PCS					I	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000286	PMID:27264673	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0004322	PMID:27264673;PMID:27868344	PCS		4/5			P	HPO:probinson[2021-08-17];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0010648	PMID:27681385	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001252	PMID:27681385;PMID:27264673	PCS		6/12			P	HPO:probinson[2021-08-17];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0004482	PMID:27264673	PCS		3/4			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001290	PMID:27264673	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0012304	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000639	PMID:27264673	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000319	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000957	PMID:27264673	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0011220	PMID:27681385	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0011461	PMID:27868344	PCS		1/1			C	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000316	PMID:27681385;PMID:28211982;PMID:27264673;PMID:27868344	PCS		9/14			P	HPO:probinson[2021-08-17];HPO:probinson[2021-05-20];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002616	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001643	OMIM:617506	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002217	PMID:27681385;PMID:27264673;PMID:27868344	PCS		6/13			P	HPO:probinson[2021-08-17];HPO:probinson[2021-05-20];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001642	PMID:27264673	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000358	PMID:27681385;PMID:28211982;PMID:27264673;PMID:27868344	PCS		8/14			P	HPO:probinson[2021-08-17];HPO:probinson[2021-05-20];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002553	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000494	PMID:27681385;PMID:28211982;PMID:27264673;PMID:27868344	PCS		5/14			P	HPO:probinson[2021-08-17];HPO:probinson[2021-05-20];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002750	PMID:27681385	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001382	PMID:27681385	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0011968	PMID:27264673	PCS		3/4			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001263	PMID:27681385;PMID:28211982;PMID:27264673;PMID:27868344	PCS		18/18			P	HPO:probinson[2021-08-17];HPO:probinson[2021-05-20];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0005180	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000609	PMID:27264673	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0009890	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000767	PMID:27681385;PMID:27868344	PCS		4/7			P	HPO:probinson[2021-08-17];HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0004969	PMID:27681385	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000329	PMID:27264673	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000207	PMID:27681385	PCS		2/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000768	PMID:28211982	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001653	PMID:27681385	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0007678	PMID:27264673	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000963	PMID:27681385	PCS		2/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000369	PMID:27681385;PMID:27264673	PCS		6/12			P	HPO:probinson[2021-05-20];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000006	PMID:27264673	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000445	PMID:27681385	PCS		2/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000687	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0005338	PMID:28211982	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001655	PMID:27681385;PMID:28211982;PMID:27868344	PCS		4/9			P	HPO:probinson[2021-08-17];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000341	PMID:28211982	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000582	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0004467	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0003577	PMID:27681385	PCS					C	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000343	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002002	PMID:28211982	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002162	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0011712	PMID:27264673	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0008070	PMID:28211982	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001629	PMID:27868344	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001508	PMID:27681385	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0012450	PMID:27681385	PCS		2/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000739	PMID:27264673	PCS		2/4			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0008872	PMID:27264673	PCS		3/4			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001305	PMID:27264673	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000219	PMID:27681385	PCS		3/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000218	PMID:27681385	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0006610	PMID:27868344	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000256	PMID:27264673	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000396	PMID:27681385	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002212	PMID:27264673	PCS		1/4			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001561	PMID:27868344	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001363	PMID:28211982	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002650	PMID:28211982	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000750	PMID:27681385	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000475	PMID:27681385;PMID:27868344	PCS		2/9			P	HPO:probinson[2021-08-17];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000430	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000391	PMID:27681385	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001480	PMID:27264673	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000193	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000470	PMID:27264673;PMID:27868344	PCS		2/5			P	HPO:probinson[2021-08-17];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001680	PMID:27681385	PCS		4/16			P	HPO:probinson[2021-08-17];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001639	PMID:27264673	PCS		0/3			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0007099	PMID:27264673	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000508	PMID:27681385;PMID:27868344	PCS		2/9			P	HPO:probinson[2021-08-17];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000348	PMID:28211982	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002208	PMID:27868344	PCS		1/1			P	HPO:probinson[2021-08-17]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0002007	PMID:27681385	PCS		1/8			P	HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000465	PMID:27681385;PMID:28211982	PCS		2/9			P	HPO:probinson[2021-08-17];HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0001631	PMID:27681385	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		HP:0000028	PMID:27264673	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-20]
OMIM:235550	Hepatic venoocclusive disease with immunodeficiency		HP:0000252	OMIM:235550	IEA					P	HPO:iea[2009-02-17]
OMIM:235550	Hepatic venoocclusive disease with immunodeficiency		HP:0001392	OMIM:235550	IEA					P	HPO:iea[2009-02-17]
OMIM:235550	Hepatic venoocclusive disease with immunodeficiency		HP:0002849	OMIM:235550	IEA					P	HPO:iea[2009-02-17]
OMIM:235550	Hepatic venoocclusive disease with immunodeficiency		HP:0000007	OMIM:235550	IEA					I	HPO:iea[2009-02-17]
OMIM:235550	Hepatic venoocclusive disease with immunodeficiency		HP:0006685	OMIM:235550	IEA					P	HPO:iea[2009-02-17]
OMIM:235550	Hepatic venoocclusive disease with immunodeficiency		HP:0002721	OMIM:235550	IEA					P	HPO:iea[2009-02-17]
OMIM:235550	Hepatic venoocclusive disease with immunodeficiency		HP:0004315	OMIM:235550	IEA					P	HPO:iea[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000483	OMIM:242900	TAS					P	HPO:iea[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0007759	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001297	PMID:16840568	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000083	OMIM:242900	TAS					P	HPO:iea[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002938	PMID:16840568;PMID:15523612	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001888	PMID:16840568	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001249	PMID:17676601;PMID:16840568	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002655	PMID:16840568	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0003521	PMID:17676601;PMID:16840568	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002076	PMID:16840568	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000097	PMID:17676601;PMID:16840568	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001263	PMID:15523612	PCS		1/1			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000691	PMID:16840568	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000093	OMIM:242900	TAS					P	HPO:iea[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0012733	PMID:15523612	PCS		1/1			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000926	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000007	PMID:11799392	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001538	PMID:16840568;PMID:15523612	PCS		3/3			P	HPO:probinson[2015-02-23];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002942	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0008689	PMID:15523612	PCS		1/1			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000325	PMID:15523612	PCS		1/1			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001034	OMIM:242900;PMID:16840568	PCS		12/12			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0003774	PMID:17676601	PCS	HP:0003621	3/3			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0003774	PMID:16840568	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0003577	PMID:17676601;PMID:16840568	PCS		4/4			C	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000100	PMID:15523612	PCS		1/1			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000100	OMIM:242900	TAS	HP:0011463	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001270	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0010701	OMIM:242900	TAS					P	HPO:skoehler[2010-06-20]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0003090	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002719	PMID:11799392;PMID:16840568	PCS		16/27			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001903	PMID:16840568	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000938	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000414	PMID:16840568	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0006453	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002515	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002637	PMID:17676601	PCS	HP:0011462	3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001945	PMID:15523612	PCS		1/1			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002634	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001620	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002213	PMID:15523612	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0004313	PMID:16840568	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001762	PMID:15523612	PCS		1/1			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000431	PMID:16840568	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0003300	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000470	PMID:15523612	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002094	PMID:16840568	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002092	PMID:16840568	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0003182	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0005280	OMIM:242900	TAS					P	HPO:iea[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001518	PMID:17676601	PCS		3/3			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000822	PMID:16840568;PMID:15523612	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002925	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002208	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002843	OMIM:242900	TAS					P	HPO:probinson[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001511	PMID:16840568;PMID:15523612	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002326	OMIM:242900	TAS	HP:0003621	3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0002326	PMID:16840568	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001510	PMID:16840568;PMID:15523612	PCS		3/3			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001873	PMID:16840568	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0000545	OMIM:242900	TAS					P	HPO:iea[2009-02-17]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001876	PMID:11799392	PCS		8/25			P	HPO:probinson[2022-08-07]
OMIM:242900	Immunoosseous dysplasia, Schimke type		HP:0001875	PMID:16840568	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-07]
OMIM:618153	Spermatogenic failure 34		HP:0033393	PMID:30137358	PCS		4/4			P	HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0032560	PMID:30137358	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0011462	PMID:30137358	PCS		4/4			C	HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0003251	PMID:30137358	PCS		4/4			P	HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0000007	PMID:30137358	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0012207	PMID:30137358	PCS		4/4			P	HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0033525	PMID:30137358	PCS		1/1			P	HPO:probinson[2022-12-20];HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0032558	PMID:30137358	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:618153	Spermatogenic failure 34		HP:0032559	PMID:30137358	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-20]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0003577	PMID:11242115	PCS		6/6			C	HPO:probinson[2022-04-28]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0033607	PMID:11242115	PCS					P	HPO:probinson[2022-04-28]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0001419	PMID:11242115	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0033222	PMID:11242115	PCS		6/6			P	HPO:probinson[2022-04-28]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0002718	PMID:11242115	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0000964	PMID:11242115	PCS		0/6			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-04-28]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0012312	PMID:11242115	PCS		4/6			P	HPO:probinson[2022-04-28]
OMIM:300299	Neutropenia, severe congenital, X-linked		HP:0001875	PMID:11242115	PCS	HP:0003577	6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000286	PMID:27964749	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0002465	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000341	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000582	PMID:27964749	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0003577	PMID:27964749	PCS		4/4			C	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0002188	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000540	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0004322	PMID:27964749	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0002002	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001274	PMID:27964749	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0012745	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000280	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000319	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0002119	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0009765	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001643	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0006610	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001763	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001249	PMID:27964749	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000358	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000110	PMID:27964749	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000154	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000494	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000252	PMID:27964749	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001762	PMID:27964749	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0031936	PMID:27964749	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0002079	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0030048	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0011968	PMID:27964749	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001263	PMID:27964749	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001680	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0010851	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0002093	PMID:27964749	PCS	HP:0003623	3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000506	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001718	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000107	PMID:27964749	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000824	PMID:27964749	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000307	PMID:27964749	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0001319	PMID:27964749	PCS		2/4			P	HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0002007	PMID:27964749	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000006	PMID:27964749	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000325	PMID:27964749	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:617260	Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies		HP:0000369	PMID:27964749	PCS		1/4			P	HPO:probinson[2022-09-26]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003376	OMIM:608340	IEA					P	HPO:iea[2009-02-17]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0001178	OMIM:608340	TAS					P	HPO:probinson[2012-07-18]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003693	OMIM:608340	TAS					P	HPO:probinson[2012-07-18]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003593	PMID:12499475	PCS		1/6			C	HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0033685	PMID:12499475	PCS		1/2			P	HPO:probinson[2023-04-22];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003690	OMIM:608340	TAS					P	HPO:iea[2009-02-17]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0034045	PMID:12499475	PCS		1/2			P	HPO:probinson[2023-04-22];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0011463	PMID:12499475	PCS		5/6			C	HPO:probinson[2012-04-11];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0007340	PMID:12499475	PCS		4/6			P	HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0009027	OMIM:608340	IEA					P	HPO:iea[2009-02-17]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0002936	PMID:12499475	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003803	PMID:12499475	PCS		1/2			P	HPO:probinson[2023-04-22];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0001765	PMID:12499475	PCS		1/6			P	HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0001265	PMID:12499475	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003445	OMIM:608340	IEA					P	HPO:iea[2009-02-17]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003387	PMID:12499475	PCS		2/2			P	HPO:probinson[2012-04-11]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0002650	OMIM:608340	TAS					P	HPO:skoehler[2013-02-25]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0001762	OMIM:608340	IEA					P	HPO:iea[2009-02-17]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0001761	OMIM:608340	IEA					P	HPO:iea[2009-02-17]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003484	PMID:12499475	PCS		3/5			P	HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0003383	PMID:12499475	PCS		2/2			P	HPO:probinson[2012-04-11];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0001284	PMID:12499475	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0011096	PMID:12499475	PCS		2/2			P	HPO:probinson[2012-04-11];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0009830	PMID:12499475	PCS		2/2			P	HPO:probinson[2012-04-11];HPO:probinson[2023-04-22]
OMIM:608340	Charcot-Marie-Tooth disease, recessive intermediate A		HP:0000007	OMIM:608340	PCS					I	HPO:probinson[2012-04-11]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0000572	PMID:12944416	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0011506	PMID:12944416	PCS					P	HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0003581	PMID:12944416	PCS					C	HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0000546	PMID:12944416	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0031531	PMID:12944416	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0007830	PMID:12944416	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0000488	PMID:12944416	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0000575	OMIM:605670	TAS					P	HPO:skoehler[2010-06-20]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0200065	PMID:12944416	PCS					P	HPO:probinson[2023-02-09]
OMIM:605670	Retinal degeneration, late-onset, autosomal dominant		HP:0000006	PMID:12944416	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-09]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0003596	PMID:8967754	PCS		2/2			C	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0000640	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002321	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0001272	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002066	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0001251	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0003690	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0000716	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0000639	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002317	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002315	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0001686	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0003326	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002312	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0000651	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002078	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0003487	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0001640	PMID:27683074	PCS		3/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0001288	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002172	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0002070	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0012378	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0012534	PMID:8967754	PCS		1/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0001635	PMID:27683074	PCS		1/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0000648	PMID:8967754;PMID:27683074	PCS		4/4			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20];HPO:probinson[2022-07-10]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0000505	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0007994	PMID:8967754	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0001638	PMID:27683074	PCS		3/3			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0000006	PMID:10976639	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0006568	PMID:27683074	PCS		1/1			P	HPO:probinson[2021-06-20]
OMIM:619259	Neurodegeneration with ataxia and late-onset optic atrophy		HP:0003535	PMID:27683074	PCS		2/2			P	HPO:probinson[2021-06-20]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000343	PMID:30122539	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0012801	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0010862	PMID:30122539	PCS		4/4			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0045074	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000316	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000637	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000219	PMID:30122539	PCS		4/4			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000455	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000256	PMID:30122539	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0001763	PMID:30122539	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000358	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0009928	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000431	PMID:30122539	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000750	PMID:30122539	PCS		4/4			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0001263	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0002194	PMID:30122539	PCS		4/4			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0001182	PMID:30122539	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0012434	PMID:30122539	PCS		3/3			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0100023	PMID:30122539	PCS		1/4			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0009890	PMID:30122539	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000729	PMID:30122539	PCS		2/4			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0004209	PMID:30122539	PCS		1/4			P	HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000006	PMID:30122539	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-28]
OMIM:618147	Intellectual developmental disorder with hypertelorism and distinctive facies		HP:0000369	PMID:30122539	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-28]
OMIM:608354	Capillary malformation-arteriovenous malformation 1		HP:0100026	PMID:14639529	PCS		8/50			P	HPO:skoehler[2015-01-27];HPO:probinson[2021-07-02]
OMIM:608354	Capillary malformation-arteriovenous malformation 1		HP:0025104	PMID:14639529	PCS		48/50			P	HPO:probinson[2021-07-02]
OMIM:608354	Capillary malformation-arteriovenous malformation 1		HP:0004947	PMID:14639529	PCS		2/50			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-02]
OMIM:608354	Capillary malformation-arteriovenous malformation 1		HP:0005306	PMID:14639529	PCS					P	HPO:probinson[2013-01-09]
OMIM:608354	Capillary malformation-arteriovenous malformation 1		HP:0000006	PMID:14639529	PCS					I	HPO:probinson[2013-03-24]
OMIM:601370	Holoprosencephaly, semilobar, with craniosynostosis		HP:0002673	OMIM:601370	IEA					P	HPO:iea[2009-02-17]
OMIM:601370	Holoprosencephaly, semilobar, with craniosynostosis		HP:0004443	OMIM:601370	IEA					P	HPO:iea[2012-02-24]
OMIM:601370	Holoprosencephaly, semilobar, with craniosynostosis		HP:0004440	OMIM:601370	IEA					P	HPO:iea[2009-02-17]
OMIM:601370	Holoprosencephaly, semilobar, with craniosynostosis		HP:0009882	OMIM:601370	PCS					P	HPO:iea[2009-02-17]
OMIM:601370	Holoprosencephaly, semilobar, with craniosynostosis		HP:0002507	OMIM:601370	IEA					P	HPO:iea[2009-02-17]
OMIM:601370	Holoprosencephaly, semilobar, with craniosynostosis		HP:0000007	OMIM:601370	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:601370	Holoprosencephaly, semilobar, with craniosynostosis		HP:0008479	OMIM:601370	IEA					P	HPO:iea[2009-02-17]
OMIM:102350	Acromial dimples		HP:0000006	OMIM:102350	IEA					I	HPO:iea[2009-02-17]
OMIM:102350	Acromial dimples		HP:0000951	OMIM:102350	IEA					P	HPO:iea[2009-02-17]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000594	PMID:21441919	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0007957	PMID:21441919	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-27]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0007968	OMIM:221900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0003577	PMID:21441919	PCS		31/31			C	HPO:probinson[2022-03-27]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0009917	OMIM:221900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000482	OMIM:221900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0011886	OMIM:221900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0008052	OMIM:221900	TAS					P	HPO:skoehler[2015-08-05]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000518	OMIM:221900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0011484	OMIM:221900	TAS					P	HPO:skoehler[2014-11-26]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0012043	OMIM:221900	TAS					P	HPO:skoehler[2013-05-31]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0032287	PMID:21441919	PCS		31/31			P	HPO:probinson[2022-03-27]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000007	PMID:21441919	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-27]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000667	OMIM:221900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000557	OMIM:221900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000612	OMIM:221900	TAS		HP:0040283			P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000568	OMIM:221900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000565	PMID:21441919	PCS		31/31			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000554	OMIM:221900	TAS		HP:0040283			P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0007899	OMIM:221900	TAS	HP:0003577				P	HPO:probinson[2013-04-01]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000501	OMIM:221900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:221900	Persistent hyperplastic primary vitreous, autosomal recessive		HP:0000555	PMID:21441919	PCS		31/31			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614594	Olmsted syndrome 1		HP:0002289	PMID:22405088	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0007759	PMID:22405088	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0007957	OMIM:614594	TAS		HP:0040283			P	HPO:skoehler[2015-01-21]
OMIM:614594	Olmsted syndrome 1		HP:0001036	OMIM:614594	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614594	Olmsted syndrome 1		HP:0002164	OMIM:614594	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614594	Olmsted syndrome 1		HP:0001371	PMID:22405088	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0003593	PMID:22405088	PCS		6/6			C	HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0034521	PMID:22405088	PCS		6/6			P	HPO:probinson[2023-06-05]
OMIM:614594	Olmsted syndrome 1		HP:0040162	PMID:22405088	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0008070	PMID:22405088	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0008392	OMIM:614594	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614594	Olmsted syndrome 1		HP:0007460	PMID:22405088	PCS		1/6			P	HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0009775	PMID:22405088	PCS		4/6			P	HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0000975	OMIM:614594	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614594	Olmsted syndrome 1		HP:0000989	PMID:22405088	PCS		6/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0008404	OMIM:614594	TAS					P	HPO:skoehler[2013-05-03]
OMIM:614594	Olmsted syndrome 1		HP:0000982	PMID:22405088	PCS		6/6			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0000006	PMID:22405088	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:614594	Olmsted syndrome 1		HP:0040009	PMID:22405088	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:256550	Neuraminidase deficiency		HP:0000023	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001310	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0004322	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0000282	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001250	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001252	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001350	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0002240	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0010729	OMIM:256550	IEA					P	HPO:skoehler[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001290	OMIM:256550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:256550	Neuraminidase deficiency		HP:0000280	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:6000911	PMID:610423	PCS		1/1			P	HPO:probinson[2024-08-04]
OMIM:256550	Neuraminidase deficiency		HP:0000518	OMIM:256550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256550	Neuraminidase deficiency		HP:0000639	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001922	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001789	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001324	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001249	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001744	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001347	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0003202	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001541	OMIM:256550	TAS					P	HPO:probinson[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001640	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0004333	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0003461	OMIM:256550	TAS					P	HPO:probinson[2012-08-04]
OMIM:256550	Neuraminidase deficiency		HP:0000093	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0010655	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0000529	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0000407	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0000943	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0000007	OMIM:256550	TAS					I	HPO:probinson[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0001638	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:256550	Neuraminidase deficiency		HP:0012061	OMIM:256550	TAS					P	HPO:probinson[2012-08-04]
OMIM:256550	Neuraminidase deficiency		HP:0001336	OMIM:256550	IEA					P	HPO:iea[2009-02-17]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000582	PMID:32710489	PCS		1/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000541	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000365	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0012745	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0005490	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0012110	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0001508	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000518	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0001548	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000316	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000238	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0007763	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0009765	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000455	PMID:32710489	PCS		1/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000278	PMID:32710489	PCS		2/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0001249	PMID:32710489	PCS		3/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0002553	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000252	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000494	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000431	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000276	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0002079	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0011968	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0001263	PMID:32710489	PCS		3/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000272	PMID:32710489	PCS		1/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000609	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0007099	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000629	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000327	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0002902	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000307	PMID:32710489	PCS		1/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000006	PMID:32710489	PCS					I	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000303	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:620157	Intellectual developmental disorder, autosomal dominant 70		HP:0000347	PMID:32710489	PCS		0/3			P	HPO:probinson[2023-06-07]
OMIM:603956	Cervical cancer		HP:0002664	PMID:10471491	PCS					P	HPO:skoehler[2013-01-10];HPO:probinson[2023-01-25]
OMIM:603956	Cervical cancer		HP:0001442	PMID:10471491	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-01-25]
OMIM:603956	Cervical cancer		HP:0030079	PMID:10471491	PCS					P	HPO:probinson[2023-01-25]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0002650	PMID:9489787	PCS		5/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0006380	PMID:9489787	PCS		4/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0004322	PMID:9489787	PCS		5/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0012894	PMID:9489787	PCS		5/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0003275	PMID:9489787	PCS		5/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0003691	PMID:9489787	PCS		4/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0003273	PMID:9489787	PCS		4/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0002938	PMID:9489787	PCS		5/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0002804	PMID:9489787	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0000774	PMID:9489787	PCS		4/5			P	HPO:probinson[2021-07-13]
OMIM:602484	Pelvic dysplasia - arthrogryposis of lower limbs		HP:0005745	PMID:9489787	PCS		5/5			P	HPO:probinson[2021-07-13]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0001374	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0001770	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0002980	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0004322	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0000141	OMIM:228930	TAS					P	HPO:skoehler[2012-10-17]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0009380	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0001849	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0006492	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0009465	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-22]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0006495	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0001802	OMIM:228930	TAS					P	HPO:skoehler[2012-10-17]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0030084	OMIM:228930	TAS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0009767	OMIM:228930	TAS					P	HPO:skoehler[2012-10-17]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0001964	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0001762	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0008839	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2009-10-22]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0001162	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0002990	OMIM:228930	IEA					P	HPO:skoehler[2015-01-27]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0006262	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-22]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0006143	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0006265	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2009-10-22]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0000007	PMID:16826533	PCS					I	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0006101	PMID:9128926	PCS		HP:0040283			P	HPO:iea[2009-10-22]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0006443	PMID:16826533	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0005914	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0002986	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2009-10-22]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0002866	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0002984	PMID:16826533	PCS		HP:0040281			P	HPO:iea[2009-10-22]
OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		HP:0005613	PMID:9128926	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:300716	Intellectual developmental disorder, X-linked 95		HP:0000750	PMID:18455129	PCS					P	HPO:probinson[2013-02-17]
OMIM:300716	Intellectual developmental disorder, X-linked 95		HP:0001417	PMID:18455129	PCS					I	HPO:probinson[2013-01-09]
OMIM:300716	Intellectual developmental disorder, X-linked 95		HP:0001423	OMIM:300716	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300716	Intellectual developmental disorder, X-linked 95		HP:0001249	PMID:18455129	PCS					P	HPO:probinson[2013-02-17]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002421	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002783	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001332	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001250	PMID:24686847	PCS		1/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002582	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001252	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0003593	PMID:24686847	PCS		1/5			C	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002061	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001290	PMID:24686847	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000639	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0003829	OMIM:615846	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0011461	PMID:24686847	PCS		2/5			C	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001249	OMIM:615846	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001369	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0003623	PMID:24686847	PCS		1/5			C	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000252	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001025	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001344	OMIM:615846	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000496	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0011968	PMID:24686847	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001263	PMID:24686847	PCS		5/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002273	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0003281	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000969	PMID:24686847	PCS		2/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0011451	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002509	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001698	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000006	PMID:24686847	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001276	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001397	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0003577	PMID:24686847	PCS		1/5			C	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000100	PMID:24686847	PCS		1/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001272	PMID:24686847	PCS		2/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002240	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0012448	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0010702	OMIM:615846	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0025085	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000737	PMID:24686847	PCS	HP:0003623	3/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001903	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001824	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001945	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001744	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002633	PMID:24686847	PCS		1/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0007229	PMID:24686847	PCS		2/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001562	PMID:24686847	PCS		2/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0008936	PMID:24686847;OMIM:615846	PCS		13/15		HP:0012828	P	HPO:probinson[2022-05-26];HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002014	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002135	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002059	PMID:24686847	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002573	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001047	OMIM:615846	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002376	PMID:24686847	PCS		1/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001285	OMIM:615846	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002090	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0012115	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001639	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000822	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001878	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000821	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0000988	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0008940	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0009710	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001511	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001873	PMID:24686847	PCS		2/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002445	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0001876	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:615846	Aicardi-Goutieres syndrome 7		HP:0002248	PMID:24686847	PCS		1/5			P	HPO:probinson[2022-05-26]
OMIM:160700	Myopia 2, autosomal dominant		HP:0000541	OMIM:160700	IEA					P	HPO:iea[2009-02-17]
OMIM:160700	Myopia 2, autosomal dominant		HP:0000707	OMIM:160700	IEA					P	HPO:iea[2009-02-17]
OMIM:160700	Myopia 2, autosomal dominant		HP:0011003	OMIM:160700	IEA					P	HPO:iea[2009-02-17]
OMIM:160700	Myopia 2, autosomal dominant		HP:0000006	OMIM:160700	TAS					I	HPO:skoehler[2013-05-29]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0004325	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0001156	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0004322	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0000023	PMID:30046013	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0003593	PMID:30046013	PCS		1/1			C	HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0002194	PMID:30046013	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0100864	PMID:30046013	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:6000819	PMID:30046013	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0000518	PMID:30046013	PCS	HP:0003593	1/1			P	HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0002808	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0001518	PMID:30046013	PCS	HP:0003577	1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0011220	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0000007	PMID:30046013	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0002515	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0000768	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0000400	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0001216	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0000358	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0004349	PMID:30046013	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:618392	Spondyloepiphyseal dysplasia, Kondo-Fu type		HP:0002655	PMID:30046013	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-01-28]
OMIM:164200	Oculodentodigital dysplasia		HP:0000286	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0001250	OMIM:164200	TAS					P	HPO:skoehler[2014-08-24]
OMIM:164200	Oculodentodigital dysplasia		HP:0002385	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000482	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0003196	PMID:15637728	PCS		4/8			P	HPO:probinson[2023-01-15]
OMIM:164200	Oculodentodigital dysplasia		HP:0001251	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0012745	OMIM:164200	TAS					P	HPO:skoehler[2014-03-24]
OMIM:164200	Oculodentodigital dysplasia		HP:0001808	OMIM:164200	TAS					P	HPO:skoehler[2014-08-24]
OMIM:164200	Oculodentodigital dysplasia		HP:0009183	PMID:15637728;OMIM:164200	PCS		15/18			P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-15]
OMIM:164200	Oculodentodigital dysplasia		HP:0000518	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000679	OMIM:164200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:164200	Oculodentodigital dysplasia		HP:0000554	PMID:15637728	PCS		8/8			P	HPO:probinson[2023-01-15]
OMIM:164200	Oculodentodigital dysplasia		HP:0002217	OMIM:164200	TAS					P	HPO:probinson[2012-03-01]
OMIM:164200	Oculodentodigital dysplasia		HP:0001249	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000011	OMIM:164200	TAS		12/20			P	HPO:skoehler[2014-08-24]
OMIM:164200	Oculodentodigital dysplasia		HP:0000175	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000252	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0001260	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000691	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0002273	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0002827	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0008442	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000568	PMID:15637728	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-15]
OMIM:164200	Oculodentodigital dysplasia		HP:0000405	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0009779	OMIM:164200	TAS					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0001257	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0002500	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000006	PMID:12457340	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-06]
OMIM:164200	Oculodentodigital dysplasia		HP:0000204	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000446	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000187	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0006801	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0010705	OMIM:164200	TAS					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000463	PMID:12457340	PCS					P	HPO:probinson[2022-11-06]
OMIM:164200	Oculodentodigital dysplasia		HP:0000581	OMIM:164200	TAS					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000460	PMID:12457340	PCS					P	HPO:probinson[2022-11-06]
OMIM:164200	Oculodentodigital dysplasia		HP:0004220	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0001592	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0011675	OMIM:164200	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:164200	Oculodentodigital dysplasia		HP:0008070	OMIM:164200	PCS					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0011359	PMID:15637728	PCS		2/8			P	HPO:skoehler[2013-08-11];HPO:probinson[2023-01-15]
OMIM:164200	Oculodentodigital dysplasia		HP:0006297	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0030084	OMIM:164200	TAS					P	HPO:skoehler[2014-09-21]
OMIM:164200	Oculodentodigital dysplasia		HP:0009765	OMIM:164200	IEA					P	HPO:skoehler[2019-02-22]
OMIM:164200	Oculodentodigital dysplasia		HP:0000218	PMID:15637728	PCS		4/8			P	HPO:probinson[2023-01-15]
OMIM:164200	Oculodentodigital dysplasia		HP:0000377	OMIM:164200	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:164200	Oculodentodigital dysplasia		HP:0002135	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0000670	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0002213	OMIM:164200	IEA					P	HPO:skoehler[2013-08-11]
OMIM:164200	Oculodentodigital dysplasia		HP:0000430	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0006480	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0002967	OMIM:164200	IEA					P	HPO:probinson[2009-02-17]
OMIM:164200	Oculodentodigital dysplasia		HP:0001631	OMIM:164200	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:164200	Oculodentodigital dysplasia		HP:0000501	PMID:15637728	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2023-01-15]
OMIM:606812	Fumarase deficiency		HP:0001399	PMID:22069215	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0003355	OMIM:606812	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606812	Fumarase deficiency		HP:0000463	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0002365	OMIM:606812	TAS					P	HPO:skoehler[2014-04-04]
OMIM:606812	Fumarase deficiency		HP:0030774	PMID:22069215	PCS		1/1			P	HPO:probinson[2023-04-22];HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0002167	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0000980	OMIM:606812	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606812	Fumarase deficiency		HP:0001274	PMID:22069215	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:606812	Fumarase deficiency		HP:0001252	PMID:22069215	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0001290	OMIM:606812	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606812	Fumarase deficiency		HP:0004482	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0001508	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0011682	PMID:22069215	PCS		1/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0000316	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0007620	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0002119	PMID:22069215	PCS		2/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0000218	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0001406	PMID:22069215	PCS		2/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0001901	OMIM:606812	TAS					P	HPO:probinson[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0001942	PMID:22069215	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:606812	Fumarase deficiency		HP:0033092	PMID:22069215	PCS		1/1			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0003128	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0002059	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0000252	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0001561	PMID:22069215	PCS		2/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0002133	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0001541	PMID:22069215	PCS		1/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0001263	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0002190	OMIM:606812	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0032106	PMID:22069215	PCS		1/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0005280	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0011129	PMID:22069215	PCS		1/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0034648	PMID:22069215	PCS		1/1			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0033165	PMID:22069215	PCS		1/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0034198	PMID:22069215	PCS		2/2			C	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0002904	OMIM:606812	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606812	Fumarase deficiency		HP:0100954	OMIM:606812	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606812	Fumarase deficiency		HP:0001339	PMID:22069215	PCS		1/2			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0000007	PMID:22069215	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0000648	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0003758	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0000505	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0002007	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:606812	Fumarase deficiency		HP:0003536	PMID:22069215	PCS		1/1			P	HPO:probinson[2023-04-22]
OMIM:606812	Fumarase deficiency		HP:0002126	OMIM:606812	IEA					P	HPO:iea[2009-02-17]
OMIM:257100	Neutropenia, lethal congenital, with eosinophilia		HP:0001880	OMIM:257100	TAS					P	HPO:probinson[2009-02-17]
OMIM:257100	Neutropenia, lethal congenital, with eosinophilia		HP:0000007	OMIM:257100	TAS					I	HPO:probinson[2009-02-17]
OMIM:257100	Neutropenia, lethal congenital, with eosinophilia		HP:0003811	OMIM:257100	TAS					C	HPO:probinson[2009-02-17]
OMIM:257100	Neutropenia, lethal congenital, with eosinophilia		HP:0001875	OMIM:257100	TAS					P	HPO:probinson[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0030854	PMID:7795640	PCS		1/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0003774	OMIM:120330	IEA		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0003577	PMID:7795640	PCS		4/4			C	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000541	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0000486	PMID:7795640	PCS		1/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000089	PMID:7795640	PCS		3/4			P	HPO:probinson[2012-07-16];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0004322	PMID:7795640	PCS		2/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000480	OMIM:120330	IEA					P	HPO:iea[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0001250	OMIM:120330	TAS					P	HPO:probinson[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0000085	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0012622	PMID:7795640	PCS		4/4			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0012595	PMID:7795640	PCS		3/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000518	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0000639	PMID:7795640	PCS		1/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0025514	OMIM:120330	TAS					P	HPO:skoehler[2017-07-13]
OMIM:120330	Papillorenal syndrome		HP:0007663	PMID:7795640	PCS		4/4			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000977	OMIM:120330	TAS					P	HPO:skoehler[2014-04-13]
OMIM:120330	Papillorenal syndrome		HP:0000974	OMIM:120330	TAS					P	HPO:skoehler[2014-04-13]
OMIM:120330	Papillorenal syndrome		HP:0001249	OMIM:120330	IEA					P	HPO:iea[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0004712	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0000533	OMIM:120330	TAS					P	HPO:skoehler[2012-10-17]
OMIM:120330	Papillorenal syndrome		HP:0011509	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0001144	OMIM:120330	IEA					P	HPO:iea[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0000076	PMID:7795640	PCS		2/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0002650	PMID:7795640	PCS		2/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0005564	PMID:7795640	PCS		1/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0001382	OMIM:120330	TAS					P	HPO:skoehler[2014-04-13]
OMIM:120330	Papillorenal syndrome		HP:0000790	PMID:7795640	PCS		2/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0002171	OMIM:120330	TAS					P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0012019	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0000093	OMIM:120330	TAS					P	HPO:probinson[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0011003	PMID:7795640	PCS		3/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000969	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0000407	PMID:7795640	PCS		1/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0007099	OMIM:120330	TAS					P	HPO:probinson[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0000608	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0000822	PMID:7795640	PCS		3/4			P	HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000107	OMIM:120330	TAS					P	HPO:probinson[2012-07-16]
OMIM:120330	Papillorenal syndrome		HP:0000568	OMIM:120330	IEA					P	HPO:iea[2009-02-17]
OMIM:120330	Papillorenal syndrome		HP:0000003	OMIM:120330	TAS					P	HPO:probinson[2012-07-16]
OMIM:120330	Papillorenal syndrome		HP:0000006	PMID:7795640	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0003259	PMID:7795640	PCS		1/1			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:120330	Papillorenal syndrome		HP:0000787	OMIM:120330	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:120330	Papillorenal syndrome		HP:0000588	PMID:7795640	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-17]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003444	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0001265	OMIM:253400	TAS					P	HPO:skoehler[2013-01-21]
OMIM:253400	Spinal muscular atrophy, type III		HP:0002378	OMIM:253400	IEA					P	HPO:iea[2009-02-17]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003621	PMID:22323744	PCS		1/2			C	HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0008946	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003676	PMID:22323744	PCS					C	HPO:skoehler[2013-01-21];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0002398	OMIM:253400	IEA					P	HPO:iea[2009-02-17]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003693	PMID:22323744	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003394	PMID:22323744	PCS		1/2			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0025708	PMID:22323744	PCS		1/2			C	HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0007340	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003749	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0000007	PMID:22323744	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0007289	OMIM:253400	IEA					P	HPO:iea[2009-02-17]
OMIM:253400	Spinal muscular atrophy, type III		HP:0001308	OMIM:253400	IEA					P	HPO:iea[2009-02-17]
OMIM:253400	Spinal muscular atrophy, type III		HP:0002505	PMID:22323744	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0007269	PMID:22323744	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003701	PMID:22323744	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003547	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003438	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0003724	PMID:22323744	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0008956	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:253400	Spinal muscular atrophy, type III		HP:0006844	PMID:22323744	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618386	Amelogenesis imperfecta, type IIIC		HP:0011084	PMID:30506946	PCS					P	HPO:probinson[2019-07-07]
OMIM:618386	Amelogenesis imperfecta, type IIIC		HP:0000705	PMID:30506946	PCS					P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618386	Amelogenesis imperfecta, type IIIC		HP:0009102	OMIM:618386	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618386	Amelogenesis imperfecta, type IIIC		HP:0006286	PMID:30506946	IEA					P	HPO:probinson[2019-07-07]
OMIM:618386	Amelogenesis imperfecta, type IIIC		HP:0000007	PMID:30506946	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0003015	PMID:29461981	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0002970	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0031936	PMID:29461981	PCS		1/2			P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0003165	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0003155	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0003021	PMID:29461981	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0011463	PMID:29461981	PCS		2/2			C	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0012052	PMID:29461981	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0012053	PMID:29461981	PCS		2/2			P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0000938	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0002979	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0002901	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0001510	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0000006	PMID:29461981	PCS					I	HPO:probinson[2020-12-05];HPO:probinson[2020-12-05]
OMIM:619073	Vitamin d-dependent rickets, type 3		HP:0002148	PMID:29461981	PCS					P	HPO:probinson[2020-12-05]
OMIM:616340	Deafness, autosomal dominant 67		HP:0000407	OMIM:616341	TAS					P	HPO:skoehler[2015-08-19]
OMIM:616340	Deafness, autosomal dominant 67		HP:0000360	OMIM:616341	TAS					P	HPO:skoehler[2015-08-19]
OMIM:616340	Deafness, autosomal dominant 67		HP:0000006	OMIM:616341	TAS					I	HPO:skoehler[2015-08-19]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001276	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003378	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003376	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003431	PMID:16835246	PCS				HP:0012825	P	HPO:probinson[2012-03-12];HPO:probinson[2020-01-06]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0000365	OMIM:609260	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003693	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001371	OMIM:609260	TAS					P	HPO:skoehler[2015-12-30]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0002460	OMIM:609260	TAS					P	HPO:probinson[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003690	OMIM:609260	TAS					P	HPO:skoehler[2013-01-22]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0012531	OMIM:609260	TAS					P	HPO:skoehler[2014-01-28]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003828	OMIM:609260	TAS					M	HPO:skoehler[2012-10-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003829	OMIM:609260	TAS					I	HPO:skoehler[2012-10-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0009027	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0002936	OMIM:609260	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003448	PMID:16835246	PCS					P	HPO:probinson[2020-01-06]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001268	OMIM:609260	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001347	OMIM:609260	IEA		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001765	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001265	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0002650	OMIM:609260	TAS					P	HPO:probinson[2012-03-12]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001761	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003487	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003383	OMIM:609260	TAS					P	HPO:probinson[2012-03-12]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001284	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003384	OMIM:609260	IEA					P	HPO:iea[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003380	OMIM:609260	TAS					P	HPO:probinson[2012-03-12]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0000648	OMIM:609260	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001257	OMIM:609260	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0000006	PMID:16835246	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-01-06]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0003677	OMIM:609260	TAS					C	HPO:probinson[2009-02-17]
OMIM:609260	Charcot-marie-tooth disease, axonal, type 2A2A		HP:0001337	OMIM:609260	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0020181	PMID:18451999	PCS		4/4			P	HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0002059	OMIM:612126	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0003621	PMID:18451999	PCS		2/4			C	HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0002353	OMIM:612126	TAS					P	HPO:skoehler[2014-05-04]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001266	OMIM:612126	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001332	OMIM:612126	TAS					P	HPO:skoehler[2013-01-22]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0002076	OMIM:612126	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001250	PMID:18451999	PCS		2/4			P	HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001263	PMID:18451999	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001251	PMID:18451999	PCS		1/4			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0003593	PMID:18451999	PCS		2/4			C	HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0002490	PMID:18451999	PCS		3/4			P	HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0011972	PMID:18451999	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0100660	PMID:18451999	PCS		4/4		HP:0025377	P	HPO:skoehler[2013-01-22];HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0000737	OMIM:612126	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0003829	OMIM:612126	TAS					I	HPO:skoehler[2012-10-17]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001878	PMID:18451999	PCS		4/4			P	HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001923	PMID:18451999	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0000006	PMID:18451999	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001337	OMIM:612126	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612126	Glut1 deficiency syndrome 2		HP:0001744	PMID:18451999	PCS		4/4			P	HPO:probinson[2022-10-03]
OMIM:615649	Deafness, autosomal dominant 54		HP:0000365	OMIM:615649	IEA					P	HPO:skoehler[2015-01-27]
OMIM:615649	Deafness, autosomal dominant 54		HP:0000006	OMIM:615649	TAS					I	HPO:skoehler[2014-02-25]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000286	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0002421	PMID:22265013	PCS	HP:0003593	7/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000340	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0031649	PMID:22265013	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000023	PMID:22265013	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0003198	PMID:24773188	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0430047	PMID:22265013	PCS		7/7			P	HPO:probinson[2024-01-13]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0430046	PMID:22265013	PCS		7/7			P	HPO:probinson[2024-01-13]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000185	PMID:22265013	PCS		2/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001252	PMID:22265013	PCS	HP:0003623	7/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000482	PMID:22265013	PCS		0/6			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001075	PMID:22265013	PCS		0/6			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001270	PMID:22265013	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0034361	PMID:24773188	PCS	HP:0003623	1/1			P	HPO:probinson[2022-10-07]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000938	OMIM:614557	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0011461	PMID:24773188	PCS		1/1			C	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000978	PMID:22265013	PCS		3/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0002515	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000977	PMID:22265013	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0003803	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000015	PMID:22265013	PCS		2/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001324	PMID:22265013	PCS	HP:0003593	7/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001643	PMID:24773188	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0007502	PMID:22265013	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000410	OMIM:614557	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001763	PMID:22265013	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000974	PMID:22265013	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000973	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0002751	PMID:22265013	PCS		5/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0003202	OMIM:614557	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0003467	OMIM:614557	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001561	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001762	OMIM:614557	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0031936	PMID:22265013	PCS		7/7			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0011968	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000592	PMID:22265013	PCS	HP:0003593	1/6			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0005180	PMID:22265013	PCS		2/5			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001757	PMID:22265013	PCS		5/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001537	PMID:22265013	PCS		3/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000007	PMID:22265013	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001558	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000601	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001319	PMID:24773188	PCS		1/1			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000405	PMID:22265013	PCS		1/6			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0001653	PMID:22265013	PCS		1/5			P	HPO:probinson[2022-04-16]
OMIM:614557	Ehlers-Danlos syndrome, kyphoscoliotic type, 2		HP:0000545	PMID:22265013	PCS		4/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-04-16]
OMIM:211800	Calcification of joints and arteries		HP:0005645	OMIM:211800	TAS					P	HPO:probinson[2021-11-11];HPO:probinson[2021-11-11]
OMIM:211800	Calcification of joints and arteries		HP:0001717	PMID:21288095	PCS		1/5			P	HPO:probinson[2021-11-11]
OMIM:211800	Calcification of joints and arteries		HP:0025477	PMID:21288095	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-11-11];HPO:probinson[2022-12-03]
OMIM:211800	Calcification of joints and arteries		HP:0011986	PMID:21288095	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-11-11];HPO:probinson[2022-12-03]
OMIM:211800	Calcification of joints and arteries		HP:0000007	PMID:21288095	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-11-11];HPO:probinson[2022-12-03]
OMIM:211800	Calcification of joints and arteries		HP:0004417	PMID:21288095	PCS		5/5			P	HPO:probinson[2021-11-11]
OMIM:211800	Calcification of joints and arteries		HP:0031303	PMID:21288095	PCS		5/5			P	HPO:probinson[2021-11-11]
OMIM:211800	Calcification of joints and arteries		HP:0031304	PMID:21288095	PCS		5/5			P	HPO:probinson[2021-11-11]
OMIM:211800	Calcification of joints and arteries		HP:0031305	PMID:21288095	PCS		4/5			P	HPO:probinson[2021-11-11]
DECIPHER:53	Prader-Willi Syndrome (Type 2)		HP:0001252	DECIPHER:53	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:53	Prader-Willi Syndrome (Type 2)		HP:0008872	DECIPHER:53	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:53	Prader-Willi Syndrome (Type 2)		HP:0001956	DECIPHER:53	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:53	Prader-Willi Syndrome (Type 2)		HP:0000135	DECIPHER:53	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:53	Prader-Willi Syndrome (Type 2)		HP:0001249	DECIPHER:53	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000341	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002069	PMID:21835305	PCS		2/2			P	HPO:probinson[2023-03-27];HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0010804	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002521	PMID:21835305	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0003577	PMID:21835305	PCS		2/2			C	HPO:skoehler[2017-07-13]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000046	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002188	PMID:21835305	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002123	PMID:21835305	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000463	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0001250	OMIM:614231	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0001252	PMID:21835305	PCS		1/2			P	HPO:skoehler[2014-11-26]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0032794	PMID:21835305	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0012594	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000819	PMID:21835305	PCS		2/2			P	HPO:skoehler[2013-01-22]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000938	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000218	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002756	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000135	PMID:21835305;OMIM:614231	PCS		3/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000212	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002910	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000952	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0001348	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0008936	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002079	OMIM:614231	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0001321	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002197	PMID:21835305	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000293	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0011968	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0001263	PMID:21835305	PCS		2/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0003241	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0010851	PMID:21835305	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0011451	PMID:21835305	PCS		2/2			P	HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000508	OMIM:614231	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000007	PMID:21835305	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000648	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0001319	OMIM:614231	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0007334	PMID:21835305	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0002205	OMIM:614231	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0001513	PMID:21835305	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0000028	OMIM:614231	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome		HP:0009879	PMID:21835305	PCS		2/2			P	HPO:skoehler[2014-11-26]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0001382	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0001263	PMID:24607389	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0001252	PMID:24607389	PCS		5/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0000086	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0002020	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0004482	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0011304	PMID:24607389	PCS		2/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0001419	PMID:24607389	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0010055	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0011220	PMID:24607389	PCS		1/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0000718	PMID:24607389	PCS		1/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0000729	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0012450	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0000722	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0002779	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0001511	PMID:24607389	PCS	HP:0011461	1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0000047	PMID:24607389	PCS		1/5			P	HPO:probinson[2021-09-28]
OMIM:300919	Intellectual developmental disorder, X-linked 99		HP:0001249	PMID:24607389	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-09-28]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000384	PMID:34313816	PCS		2/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0002783	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001250	PMID:34313816	PCS		2/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001252	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0003593	PMID:34313816	PCS		3/3			C	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0002061	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0012444	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000819	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001508	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000938	PMID:34313816	PCS		1/2			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001822	PMID:34313816	PCS		2/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001847	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0030084	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000218	PMID:34313816	PCS		2/3			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001249	PMID:34313816	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000252	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001684	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0011968	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000490	PMID:34313816	PCS		2/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001263	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0011304	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0001518	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000448	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000007	PMID:26633546	PCS					I	HPO:probinson[2023-04-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0430028	PMID:34313816	PCS		2/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0200134	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000768	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000400	PMID:34313816	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000567	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:620194	Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies		HP:0000347	PMID:34313816	PCS		1/3			P	HPO:probinson[2023-06-11]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002069	PMID:34800363	PCS		5/9			P	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0030799	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0003577	PMID:34800363	PCS		1/9			C	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002521	PMID:34800363	PCS		1/5			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002540	PMID:28017472	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000365	PMID:34800363	PCS		4/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0001251	PMID:28017472	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0003593	PMID:28017472;PMID:34800363	PCS		7/10			C	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0012469	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0001508	PMID:28017472	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000639	PMID:34800363	PCS		2/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000338	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0006970	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002119	PMID:28017472	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000218	PMID:34800363	PCS		2/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0001488	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000252	PMID:28017472	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0003621	PMID:34800363	PCS		2/9			C	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0001385	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000494	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002059	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002133	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002650	PMID:34800363	PCS		2/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0002079	PMID:28017472;PMID:34800363	PCS		2/10			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0001761	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0001263	PMID:34800363	PCS		8/9			P	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0011344	PMID:28017472	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000007	PMID:28017472	PCS					I	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000505	PMID:34800363	PCS		3/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0000648	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0011170	PMID:34800363	PCS		1/9			P	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:619701	Yoon-Bellen neurodevelopmental syndrome		HP:0001257	PMID:28017472	PCS		1/1			P	HPO:probinson[2022-03-19]
DECIPHER:47	RCAD (renal cysts and diabetes)		HP:0000819	DECIPHER:47	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:47	RCAD (renal cysts and diabetes)		HP:0001392	DECIPHER:47	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:47	RCAD (renal cysts and diabetes)		HP:0005562	DECIPHER:47	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614225	Warburg micro syndrome 2		HP:0003577	PMID:20967465	PCS		1/1			C	HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0011918	PMID:20967465	PCS		1/1			P	HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000046	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0001371	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0002283	PMID:20967465	PCS		1/1			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000482	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0003196	PMID:20967465	PCS		1/1			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0001252	PMID:20967465	PCS		1/1			P	HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0010722	PMID:20967465	PCS		1/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000518	PMID:20967465	PCS	HP:0003577	1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000519	OMIM:614225	TAS				HP:0012832	P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0001845	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0008897	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0000059	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0007965	OMIM:614225	TAS					P	HPO:probinson[2013-08-10]
OMIM:614225	Warburg micro syndrome 2		HP:0001864	PMID:20967465	PCS		1/1			P	HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0008936	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0000252	PMID:20967465	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000054	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0001264	OMIM:614225	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614225	Warburg micro syndrome 2		HP:0001344	PMID:20967465	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0002079	PMID:20967465	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000490	PMID:20967465	PCS		1/1			P	HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0001263	PMID:20967465	PCS		1/1			P	HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000294	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0005484	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0011344	OMIM:614225	TAS					P	HPO:probinson[2013-08-10]
OMIM:614225	Warburg micro syndrome 2		HP:0000426	PMID:20967465	PCS		1/1			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000007	PMID:20967465	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000568	PMID:20967465	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000648	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0000400	PMID:20967465	PCS		1/1			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000248	PMID:20967465	PCS		1/1			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-12-14]
OMIM:614225	Warburg micro syndrome 2		HP:0000028	OMIM:614225	TAS					P	HPO:skoehler[2014-04-04]
OMIM:614225	Warburg micro syndrome 2		HP:0002126	PMID:20967465	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-12-14]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0004798	OMIM:612132	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0000970	OMIM:612132	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0002046	OMIM:612132	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0003593	PMID:14523047	PCS		1/1			C	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0002240	PMID:14523047	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0011136	OMIM:612132	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0011114	OMIM:612132	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0008070	OMIM:612132	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0001508	PMID:14523047	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0000958	PMID:14523047	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0011120	OMIM:612132	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0000668	OMIM:612132	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0002209	PMID:14523047	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0007476	PMID:14523047	PCS		1/1			P	HPO:skoehler[2015-01-14];HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0000966	OMIM:612132	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0002007	OMIM:612132	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0002205	PMID:14523047	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0000006	PMID:14523047	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0001744	PMID:14523047	PCS		1/1			P	HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0000698	PMID:14523047	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:612132	Ectodermal dysplasia and immunodeficiency 2		HP:0002028	PMID:14523047	PCS	HP:0003593	1/1			P	HPO:probinson[2023-02-10]
OMIM:615885	Hypotrichosis 12		HP:0000164	PMID:21412954	PCS		0/13			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0001597	PMID:21412954	PCS		0/13			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0003593	PMID:21412954	PCS		13/13			C	HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0011359	PMID:21412954	PCS		13/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0100840	PMID:21412954	PCS		10/13			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0002209	PMID:21412954	PCS		13/13			P	HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0200102	PMID:21412954	PCS		12/13			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0000971	PMID:21412954	PCS		0/13			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0002217	PMID:21412954	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0000006	PMID:21412954	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0002225	PMID:21412954	PCS		10/12			P	HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0000951	PMID:21412954	PCS		0/13			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-06-04]
OMIM:615885	Hypotrichosis 12		HP:0002215	PMID:21412954	PCS		12/13			P	HPO:probinson[2023-06-04]
OMIM:610725	Nephrotic syndrome, type 3		HP:0003774	PMID:17086182	PCS		11/14			P	HPO:probinson[2012-07-15];HPO:probinson[2023-02-21]
OMIM:610725	Nephrotic syndrome, type 3		HP:0003676	PMID:17086182	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:610725	Nephrotic syndrome, type 3		HP:0003621	PMID:17086182	PCS		1/14			C	HPO:probinson[2023-02-21]
OMIM:610725	Nephrotic syndrome, type 3		HP:0000100	PMID:17086182	PCS		14/14			P	HPO:probinson[2012-07-15];HPO:probinson[2023-02-21]
OMIM:610725	Nephrotic syndrome, type 3		HP:0000969	OMIM:610725	TAS					P	HPO:probinson[2009-02-17]
OMIM:610725	Nephrotic syndrome, type 3		HP:0011463	PMID:17086182	PCS		6/14			C	HPO:probinson[2009-02-17];HPO:probinson[2023-02-21]
OMIM:610725	Nephrotic syndrome, type 3		HP:0000097	PMID:17086182	PCS		3/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-21]
OMIM:610725	Nephrotic syndrome, type 3		HP:0003593	PMID:17086182	PCS		7/14			C	HPO:probinson[2023-02-21]
OMIM:610725	Nephrotic syndrome, type 3		HP:0003073	OMIM:610725	TAS					P	HPO:probinson[2009-02-17]
OMIM:610725	Nephrotic syndrome, type 3		HP:0000007	OMIM:610725	TAS					I	HPO:probinson[2009-02-17]
OMIM:610725	Nephrotic syndrome, type 3		HP:0000093	OMIM:610725	TAS					P	HPO:probinson[2009-02-17]
OMIM:610725	Nephrotic syndrome, type 3		HP:0001967	PMID:17086182	PCS		8/10			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-21]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000365	PMID:30533525	PCS		1/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002166	PMID:30533525	PCS		9/40			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0003552	PMID:30533525	PCS		32/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001310	PMID:30533525	PCS		13/35			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001272	PMID:17646629;PMID:30533525	PCS		41/43			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002120	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002066	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000020	PMID:17646629	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001350	PMID:30533525	PCS		32/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002064	OMIM:607259	IEA		2/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002061	PMID:17646629	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0033051	PMID:17646629	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0100543	OMIM:607259	TAS					P	HPO:probinson[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000639	PMID:17646629;PMID:30533525	PCS		18/45			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0007340	PMID:17646629;PMID:30533525	PCS		11/45			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0011462	PMID:17646629	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002839	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002515	PMID:30533525	PCS		4/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0006895	PMID:30533525	PCS		39/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001324	PMID:30533525	PCS		19/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002314	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001347	PMID:30533525	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000511	PMID:30533525	PCS		1/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002015	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0003621	PMID:17646629	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002650	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0003487	PMID:17646629;PMID:30533525	PCS		22/42			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001288	PMID:17646629	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002354	PMID:17646629	PCS		2/3			P	HPO:probinson[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001761	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002497	PMID:30533525	PCS		33/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000012	OMIM:607259	IEA					P	HPO:iea[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002395	PMID:17646629	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0003484	PMID:17646629;PMID:30533525	PCS		3/39			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001260	PMID:17646629	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0003581	PMID:30533525	PCS					C	HPO:probinson[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002075	PMID:30533525	PCS		16/35			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0200049	PMID:30533525	PCS		5/34			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002172	PMID:30533525	PCS		41/42			P	HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0002070	PMID:17646629	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0007350	PMID:17646629	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000605	PMID:17646629	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0007377	PMID:17646629	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000007	PMID:30533525	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000648	OMIM:607259	IEA		1/42			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-06]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0001258	OMIM:607259	TAS					P	HPO:probinson[2009-02-17]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0000006	OMIM:607259	TAS					I	HPO:skoehler[2013-05-03]
OMIM:607259	Spastic paraplegia 7, autosomal recessive		HP:0006986	PMID:17646629	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0001276	PMID:30595371	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000341	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0003577	PMID:30595371	PCS		3/3			C	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0002188	PMID:30595371	PCS		1/2			P	HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000023	PMID:30595371	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0001371	PMID:30595371	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0001250	PMID:30595371	PCS		3/3			P	HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0003196	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000518	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0001508	PMID:30595371	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0100704	PMID:30595371	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000737	PMID:30595371	PCS		2/3			P	HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000711	PMID:30595371	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0008872	PMID:30595371	PCS		2/3			P	HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0001385	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000252	PMID:30595371	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0002650	PMID:30595371	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0002750	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0002079	PMID:30595371	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000331	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0011800	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000407	PMID:30595371	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0200134	PMID:30595371	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000006	PMID:30595371	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:618379	Developmental and epileptic encephalopathy 73		HP:0000446	PMID:30595371	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-16]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0001762	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0002650	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0003273	OMIM:118650	TAS					P	HPO:probinson[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0008070	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0010655	OMIM:118650	TAS					P	HPO:probinson[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0007390	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0006380	OMIM:118650	TAS					P	HPO:probinson[2012-07-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0011892	OMIM:118650	TAS					P	HPO:skoehler[2015-01-21]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0000518	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0002208	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0002007	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0008855	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0000006	OMIM:118650	IEA					I	HPO:iea[2009-02-17]
OMIM:118650	Chondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiency, included		HP:0004646	OMIM:118650	IEA					P	HPO:iea[2009-02-17]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000286	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0002540	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000365	PMID:25848753	PCS		5/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000684	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001250	PMID:25848753	PCS		8/22			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0002186	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001252	PMID:25848753;PMID:25439728	PCS		28/29			P	HPO:probinson[2022-12-13];HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0003593	OMIM:616354	TAS		2/22			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000283	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001251	PMID:25439728	PCS		5/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0012745	PMID:25439728	PCS		6/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0004482	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000280	PMID:25848753;PMID:25439728	PCS		29/29			P	HPO:probinson[2022-12-13];HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000639	PMID:25848753	PCS		11/22			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0011463	PMID:25848753	PCS		18/22			C	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0012471	PMID:25439728	PCS		7/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0011220	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000998	PMID:25848753	PCS		12/22			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000678	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0025336	PMID:25439728	PCS		6/7			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000158	PMID:25848753	PCS		12/22			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001249	PMID:25439728	PCS		6/6			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0003623	PMID:25848753	PCS		2/22			C	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0002751	PMID:25848753	PCS		10/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001265	OMIM:616354	TAS		5/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001344	PMID:25439728	PCS		5/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0003487	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001263	OMIM:616354	TAS				HP:0012828	P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0002194	PMID:25848753	PCS		22/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0012810	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0012385	PMID:25439728	PCS		6/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000407	OMIM:616354	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000729	PMID:25848753	PCS		12/22			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000007	PMID:25439728	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001257	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000289	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000343	PMID:25439728	PCS		6/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001156	PMID:25439728	PCS		6/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000463	OMIM:616354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0002120	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001272	PMID:25848753;PMID:25439728	PCS		27/29			P	HPO:probinson[2022-12-13];HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0002240	PMID:25848753	PCS		5/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0010862	PMID:25848753	PCS		22/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0010471	PMID:25848753	PCS		5/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000414	PMID:25439728	PCS		7/7			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000218	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0030084	PMID:25848753	PCS		10/22			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001744	PMID:25848753	PCS		5/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001762	PMID:25439728	PCS		3/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0002650	PMID:25439728	PCS		2/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0000750	PMID:25848753	PCS		22/22			P	HPO:probinson[2022-12-13]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0001321	OMIM:616354	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20		HP:0012434	PMID:25848753	PCS		22/22			P	HPO:probinson[2022-12-13]
OMIM:271110	Spinal muscular atrophy with microcephaly and mental subnormality		HP:0000252	OMIM:271110	IEA					P	HPO:iea[2009-02-17]
OMIM:271110	Spinal muscular atrophy with microcephaly and mental subnormality		HP:0006959	OMIM:271110	IEA					P	HPO:iea[2009-02-17]
OMIM:271110	Spinal muscular atrophy with microcephaly and mental subnormality		HP:0000007	OMIM:271110	IEA					I	HPO:iea[2009-02-17]
OMIM:271110	Spinal muscular atrophy with microcephaly and mental subnormality		HP:0001249	OMIM:271110	IEA					P	HPO:iea[2009-02-17]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0003202	OMIM:613204	TAS					P	HPO:skoehler[2013-06-03]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0000473	PMID:9590299	PCS		2/3			P	HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0003236	PMID:9590299	PCS		2/3		HP:0012825	P	HPO:probinson[2013-06-02];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0003577	PMID:9590299	PCS		1/3			C	HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0002650	OMIM:613204	TAS					P	HPO:skoehler[2013-06-03]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0001252	PMID:9590299	PCS	HP:0003577	1/3			P	HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0003560	PMID:9590299	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0003593	PMID:9590299	PCS		2/3			C	HPO:skoehler[2013-06-03];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0012548	PMID:9590299	PCS					P	HPO:probinson[2014-01-01];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0001270	PMID:9590299	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0003391	PMID:9590299	PCS		1/3			P	HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0000007	PMID:9590299	PCS					I	HPO:skoehler[2013-06-03];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0001324	PMID:9590299	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0001249	OMIM:613204	TAS		1/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-10-10]
OMIM:613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency		HP:0003557	PMID:9590299	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-10-10]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0005425	PMID:12353035	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0002850	PMID:12353035	PCS		1/2			P	HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0004322	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0410300	PMID:12353035	PCS		2/2			P	HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0002099	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0005353	PMID:12353035	PCS		2/2			P	HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0005384	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0033278	PMID:12353035	PCS		2/2			P	HPO:probinson[2020-12-07]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0002090	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0001508	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0033222	PMID:12353035	PCS		2/2			P	HPO:probinson[2020-12-07]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0000007	PMID:12353035	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0000964	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0002716	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0005419	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0001744	PMID:12353035	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0002720	PMID:12353035	PCS		1/2			P	HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0002028	PMID:12353035	PCS		1/2			P	HPO:probinson[2012-06-08];HPO:probinson[2020-11-27]
OMIM:607271	Autoimmune lymphoproliferative syndrome, type IIB		HP:0004315	PMID:12353035	PCS		1/2			P	HPO:probinson[2020-11-27]
OMIM:150600	Legg-Calve-Perthes disease		HP:0005743	OMIM:150600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:150600	Legg-Calve-Perthes disease		HP:0002750	OMIM:150600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:150600	Legg-Calve-Perthes disease		HP:0004322	OMIM:150600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:150600	Legg-Calve-Perthes disease		HP:0001426	OMIM:150600	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:150600	Legg-Calve-Perthes disease		HP:0000006	OMIM:150600	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000286	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000463	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001156	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000023	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0010808	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001252	PMID:27048600	PCS		4/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001251	PMID:27048600	PCS		2/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0003593	PMID:27048600	PCS		5/5			C	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0025161	PMID:27048600	PCS		2/5			P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001508	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0010055	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000316	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000954	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001627	PMID:27048600	PCS		0/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000219	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000537	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000218	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000378	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001302	PMID:27048600	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0002019	PMID:27048600	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001249	PMID:27048600	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0004315	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0002553	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000396	PMID:27048600	PCS		2/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0004313	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000252	PMID:27048600	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001561	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001344	PMID:27048600	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000750	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0002650	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000431	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0031936	PMID:27048600	PCS		5/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0011968	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001382	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0010819	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001263	PMID:27048600	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0100023	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000508	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0001537	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0004209	PMID:27048600	PCS		1/5			P	HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000664	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0007018	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000006	PMID:27048600	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0002720	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000369	PMID:27048600	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0000347	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617062	Okur-Chung neurodevelopmental syndrome		HP:0009879	PMID:27048600	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0003577	PMID:30715179	PCS		3/3			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0000750	PMID:30715179	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0002144	PMID:30715179	PCS		1/3			P	HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:6000184	PMID:30715179	PCS		1/3			P	HPO:probinson[2024-04-03]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0002079	PMID:30715179	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0001263	PMID:30715179	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0011451	PMID:30715179	PCS	HP:0003577	3/3			P	HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0000007	PMID:30715179	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0007018	PMID:30715179	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:618351	Microcephaly 25, primary, autosomal recessive		HP:0001249	PMID:30715179	PCS		3/3			P	HPO:probinson[2022-10-01]
OMIM:620816	MHC class II deficiency 3		HP:0005403	PMID:37584719;PMID:30170160	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0002850	PMID:37584719;PMID:30170160	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0002840	PMID:37584719	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0020086	PMID:37584719;PMID:30170160	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0002110	PMID:38441205	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0004385	PMID:37584719;PMID:30170160;PMID:38441205	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0020087	PMID:30170160	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0003593	PMID:37584719;PMID:30170160;PMID:38441205	PCS		8/8			C	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0003095	PMID:38441205	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0010976	PMID:37584719;PMID:30170160	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0031390	PMID:37584719;PMID:30170160;PMID:38441205	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0009098	PMID:30170160;PMID:38441205	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0001508	PMID:37584719;PMID:30170160	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0100658	PMID:37584719	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0100806	PMID:30170160;PMID:38441205	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0000403	PMID:37584719;PMID:30170160	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0000007	PMID:30170160	PCS					I	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0006532	PMID:37584719;PMID:30170160;PMID:38441205	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0002720	PMID:37584719;PMID:30170160	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0001744	PMID:37584719	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0002754	PMID:38441205	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:620816	MHC class II deficiency 3		HP:0004315	PMID:37584719	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-10-19]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0002521	PMID:29410512	PCS	HP:0003593	3/3			P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000340	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000582	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0001410	OMIM:618437	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000463	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0001250	PMID:29410512	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0002120	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0003196	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0100704	OMIM:618437	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000316	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0008872	PMID:29410512	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0003429	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0006579	PMID:29410512	PCS	HP:0003623	2/3			P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0001347	OMIM:618437	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0008936	OMIM:618437	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0001344	PMID:29410512	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000431	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0006913	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0003487	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000331	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0002079	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000194	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0001263	PMID:29410512	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0005484	PMID:29410512	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0012736	OMIM:618437	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000007	PMID:29410512	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0001638	OMIM:618437	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000648	OMIM:618437	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0200134	OMIM:618437	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000543	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000520	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0000322	PMID:29410512	PCS					P	HPO:probinson[2019-07-07]
OMIM:618437	Epileptic encephalopathy, early infantile, 75		HP:0001257	OMIM:618437	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000286	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0003577	PMID:12514359	PCS		2/2			C	HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0001156	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000463	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000160	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0001290	PMID:12514359	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0002282	PMID:12514359	PCS		1/1			P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0011220	PMID:12514359	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0025116	PMID:12514359	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000179	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000410	PMID:12514359	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000215	PMID:12514359	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000396	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000430	PMID:12514359	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0002750	PMID:12514359	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000293	PMID:12514359	PCS		2/2			P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000391	PMID:12514359	PCS		2/2			P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0001263	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0011800	PMID:12514359	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0005280	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000508	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0001998	PMID:12514359	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000007	OMIM:608624	IEA					I	HPO:iea[2009-02-17]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0001319	PMID:12514359	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000527	PMID:12514359	PCS		2/2			P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0002007	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0001513	PMID:12514359	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0000369	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:608624	Midface hypoplasia, obesity, developmental delay, and neonatal hypotonia		HP:0007933	PMID:12514359	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:154300	Malocclusion due to protuberant upper front teeth		HP:0000689	OMIM:154300	IEA					P	HPO:iea[2009-02-17]
OMIM:154300	Malocclusion due to protuberant upper front teeth		HP:0000006	OMIM:154300	IEA					I	HPO:iea[2009-02-17]
OMIM:615113	Microphthalmia, isolated 8		HP:0000609	PMID:23591992;PMID:23312594	PCS		3/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-08-06];HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0003577	PMID:23591992;PMID:23312594	PCS		6/6			C	HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0000541	PMID:23591992	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0000480	PMID:23591992	PCS		1/3			P	HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0000528	PMID:23591992;PMID:23312594	PCS		4/6			P	HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0034311	PMID:23591992;PMID:23312594	PCS		3/6			P	HPO:probinson[2022-09-05]
OMIM:615113	Microphthalmia, isolated 8		HP:0012745	PMID:23591992	PCS		2/3			P	HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0011478	PMID:23591992	PCS		1/3			P	HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0000568	PMID:23591992;PMID:23312594	PCS		3/6			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-08-06];HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0000007	PMID:23312594	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-08-06]
OMIM:615113	Microphthalmia, isolated 8		HP:0000621	PMID:23591992	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-06]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0001640	OMIM:613576	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0000968	OMIM:613576	IEA					P	HPO:skoehler[2015-01-14]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0006297	OMIM:613576	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0007475	OMIM:613576	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0000007	OMIM:613576	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0000975	OMIM:613576	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0000219	OMIM:613576	TAS					P	HPO:skoehler[2013-05-31]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0000400	OMIM:613576	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0001159	OMIM:613576	IEA					P	HPO:skoehler[2015-12-30]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0007502	OMIM:613576	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0000982	OMIM:613576	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613576	Ectodermal dysplasia-syndactyly syndrome 2		HP:0008070	OMIM:613576	TAS					P	HPO:skoehler[2012-10-17]
OMIM:190430	Triglyceride storage disease, type II		HP:0001513	OMIM:190430	TAS					P	HPO:probinson[2009-02-17]
OMIM:190430	Triglyceride storage disease, type II		HP:0000006	OMIM:190430	TAS					I	HPO:probinson[2015-02-25]
OMIM:614219	Adams-Oliver syndrome 2		HP:0003577	PMID:21820096	PCS		2/2			C	HPO:probinson[2023-03-18];HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001792	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000486	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001596	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001057	PMID:21820096	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001250	PMID:21820096	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001252	OMIM:614219	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000519	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0005807	PMID:21820096	PCS		2/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000316	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000954	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000414	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000238	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000411	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0006951	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000256	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0008936	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001562	PMID:21820096	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0002059	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0006956	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000252	PMID:21820096	PCS		1/2			P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000750	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001321	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001263	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000294	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0045025	OMIM:614219	TAS					P	HPO:skoehler[2014-11-27]
OMIM:614219	Adams-Oliver syndrome 2		HP:0011344	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0005280	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0002509	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0005819	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000965	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000007	PMID:21820096	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0001558	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000568	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000648	PMID:21820096;OMIM:614219	PCS		3/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000505	PMID:21820096	PCS		1/2			P	HPO:probinson[2023-03-18]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000369	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0000347	OMIM:614219	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614219	Adams-Oliver syndrome 2		HP:0002126	OMIM:614219	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:615107	Cowden syndrome 4		HP:0003002	PMID:21177507	PCS					P	HPO:probinson[2022-04-11]
OMIM:615107	Cowden syndrome 4		HP:0500009	PMID:21177507	PCS					P	HPO:probinson[2022-04-11]
OMIM:615107	Cowden syndrome 4		HP:0010566	PMID:21177507	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2022-04-11]
OMIM:615107	Cowden syndrome 4		HP:0012844	PMID:21177507	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2022-04-11]
OMIM:615107	Cowden syndrome 4		HP:0000256	PMID:21177507	PCS					P	HPO:probinson[2022-04-11]
OMIM:615107	Cowden syndrome 4		HP:0009726	PMID:21177507	PCS					P	HPO:skoehler[2015-08-26];HPO:probinson[2022-04-11]
OMIM:267000	Perlman syndrome		HP:0010804	OMIM:267000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267000	Perlman syndrome		HP:0010803	PMID:22306653	PCS		7/7			P	HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0001274	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0200116	OMIM:267000	TAS					P	HPO:skoehler[2013-06-10]
OMIM:267000	Perlman syndrome		HP:0002580	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0011611	OMIM:267000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267000	Perlman syndrome		HP:0003271	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0001507	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0011341	OMIM:267000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267000	Perlman syndrome		HP:0008696	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0001943	PMID:22306653	PCS		2/5			P	HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0001626	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0000776	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0001561	PMID:22306653	PCS		4/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0005247	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0001520	PMID:22306653	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0004510	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0000431	PMID:22306653	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0001541	OMIM:267000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267000	Perlman syndrome		HP:0000194	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0001263	PMID:22306653	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0005280	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0100880	OMIM:267000	TAS					P	HPO:skoehler[2014-01-28]
OMIM:267000	Perlman syndrome		HP:0000969	OMIM:267000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267000	Perlman syndrome		HP:0001999	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0000007	PMID:22306653	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0008643	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0002667	PMID:22306653	PCS		4/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:267000	Perlman syndrome		HP:0000028	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:267000	Perlman syndrome		HP:0000369	OMIM:267000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267000	Perlman syndrome		HP:0000347	OMIM:267000	IEA					P	HPO:iea[2009-02-17]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001276	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000486	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000343	PMID:28236339	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002188	PMID:28650581	PCS		1/1			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002167	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001332	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001310	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001250	OMIM:617710	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001272	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001251	PMID:28236339	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0003593	PMID:28650581	PCS		1/1			C	HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0025162	PMID:28236339	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000639	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000718	PMID:28236339	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001943	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002119	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000510	OMIM:617710	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001324	PMID:28236339	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001249	PMID:28236339;PMID:28650581	PCS		3/3			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19];HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0003128	OMIM:617710	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001347	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0003700	PMID:28650581	PCS		1/1			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000577	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0003202	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0008936	OMIM:617710;PMID:28650581	PCS		11/11			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19];HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002510	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002059	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001344	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0011968	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002352	PMID:28650581	PCS		1/1			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001260	PMID:28236339	PCS		2/2			P	HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002151	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001263	PMID:28236339;PMID:28650581	PCS		3/3			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19];HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0031165	PMID:28650581	PCS		1/1			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002509	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002506	PMID:28650581	PCS		1/1			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000646	PMID:28650581	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000007	PMID:28236339	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0000648	OMIM:617710	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001638	OMIM:617710	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001511	OMIM:617710	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001873	PMID:28650581	PCS		1/1			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0002305	PMID:28236339	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-19]
OMIM:617710	Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures		HP:0001337	PMID:28650581	PCS		1/1			P	HPO:probinson[2022-04-19];HPO:probinson[2022-04-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000561	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000164	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000160	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0003196	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0012745	OMIM:608156	TAS					P	HPO:skoehler[2014-03-24]
OMIM:608156	Nablus mask-like facial syndrome		HP:0045075	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-05-08];HPO:probinson[2022-07-10];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000319	PMID:12923873	PCS		1/1			P	HPO:probinson[2012-05-01];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000316	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000954	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0003745	PMID:12923873	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000278	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000358	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0002553	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000054	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000298	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0001263	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000294	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0001182	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0012385	OMIM:608156	TAS					P	HPO:skoehler[2013-10-22]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000327	PMID:12923873	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000007	OMIM:608156	IEA					I	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0001852	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000006	PMID:12923873	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000369	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000066	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000341	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000385	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0003577	PMID:12923873	PCS		1/1			C	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000343	PMID:12923873	PCS		1/1			P	HPO:probinson[2012-05-01];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000463	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0010109	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000581	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0040082	OMIM:608156	TAS					P	HPO:skoehler[2014-11-27]
OMIM:608156	Nablus mask-like facial syndrome		HP:0008070	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000219	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0030084	OMIM:608156	TAS					P	HPO:skoehler[2014-09-21]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000218	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0002557	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000653	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0006610	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0002236	PMID:12923873	PCS		1/1			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000396	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0001363	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000475	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000431	PMID:12923873	PCS		1/1			P	HPO:probinson[2012-05-01];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000232	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0002057	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0005484	PMID:12923873	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000470	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0011823	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0005280	PMID:12923873	PCS		1/1			P	HPO:probinson[2012-05-01];HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0009473	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000506	PMID:12923873	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:608156	Nablus mask-like facial syndrome		HP:0002007	OMIM:608156	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608156	Nablus mask-like facial syndrome		HP:0000028	OMIM:608156	IEA					P	HPO:skoehler[2010-06-19]
OMIM:618345	Retinitis pigmentosa 85		HP:0000007	PMID:29726989	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:618345	Retinitis pigmentosa 85		HP:0007663	PMID:29726989	PCS	HP:0003621	2/2			P	HPO:probinson[2019-09-07];HPO:probinson[2019-10-04]
OMIM:618345	Retinitis pigmentosa 85		HP:0007675	PMID:29726989	PCS		2/2			P	HPO:probinson[2019-10-04];HPO:probinson[2019-10-04]
OMIM:618345	Retinitis pigmentosa 85		HP:0000510	PMID:29726989	PCS					P	HPO:probinson[2019-09-07]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0002630	OMIM:214950	TAS					P	HPO:probinson[2014-01-01]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0031956	PMID:12512044	PCS		1/1			P	HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0030985	PMID:12512044	PCS		1/1			P	HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0001399	OMIM:214950	IEA					P	HPO:skoehler[2010-06-20]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0002573	PMID:12512044	PCS		1/1			P	HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0002240	PMID:12512044	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0200084	PMID:12512044	PCS		1/1			P	HPO:skoehler[2013-06-04]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0100513	PMID:12512044	PCS		1/1			P	HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0008151	PMID:12512044	PCS		1/1			P	HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0001508	OMIM:214950	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0002904	PMID:12512044	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0012053	PMID:12512044	PCS		1/1			P	HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0000007	PMID:12512044	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0001406	OMIM:214950	IEA					P	HPO:iea[2009-02-17]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0002910	OMIM:214950	IEA					P	HPO:iea[2009-02-17]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0006579	OMIM:214950	IEA					P	HPO:iea[2009-02-17]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0003645	PMID:12512044	PCS		1/1			P	HPO:probinson[2023-03-15]
OMIM:214950	Bile acid synthesis defect, congenital, 4		HP:0003623	PMID:12512044	PCS		1/1			C	HPO:iea[2009-02-17]
OMIM:616368	CHOPS syndrome		HP:0003577	PMID:25730767	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000343	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000365	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0006528	PMID:25730767	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0004322	PMID:25730767	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001156	PMID:25730767	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000463	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0003196	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000085	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002020	PMID:25730767	PCS		2/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000280	PMID:25730767	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0011951	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000518	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001629	PMID:25730767	PCS		2/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000316	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002779	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002714	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001643	PMID:25730767	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000311	PMID:25730767	PCS		2/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002019	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001601	PMID:25730767	PCS		2/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001249	PMID:25730767	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001744	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002578	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002212	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000076	PMID:25730767	PCS		2/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000252	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000574	PMID:25730767	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000391	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001263	PMID:25730767	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0010772	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0010535	PMID:25730767	PCS		2/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0100874	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002705	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000648	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000527	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0002208	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000664	PMID:25730767	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000520	PMID:25730767	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001513	PMID:25730767	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000028	PMID:25730767	PCS		1/1	MALE		P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0000006	PMID:25730767	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0004602	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:616368	CHOPS syndrome		HP:0001655	PMID:25730767	PCS		1/3			P	HPO:probinson[2022-09-22]
OMIM:611407	Cardiomyopathy, dilated, 1W		HP:0003596	PMID:11815424	PCS		1/3			C	HPO:probinson[2022-07-03]
OMIM:611407	Cardiomyopathy, dilated, 1W		HP:0011462	PMID:11815424	PCS		2/3			C	HPO:probinson[2022-07-03]
OMIM:611407	Cardiomyopathy, dilated, 1W		HP:0012664	PMID:11815424	PCS		2/3			P	HPO:probinson[2022-07-03]
OMIM:611407	Cardiomyopathy, dilated, 1W		HP:0033755	PMID:11815424	PCS		3/3			P	HPO:probinson[2022-07-03]
OMIM:611407	Cardiomyopathy, dilated, 1W		HP:0000006	PMID:11815424	PCS					I	HPO:probinson[2013-04-01]
OMIM:611407	Cardiomyopathy, dilated, 1W		HP:0001644	PMID:11815424	PCS		3/3			P	HPO:probinson[2013-01-09];HPO:probinson[2022-07-03]
OMIM:605472	Usher syndrome, type IIC		HP:0000007	OMIM:605472	IEA					I	HPO:iea[2009-02-17]
OMIM:605472	Usher syndrome, type IIC		HP:0000510	OMIM:605472	IEA					P	HPO:iea[2009-02-17]
OMIM:605472	Usher syndrome, type IIC		HP:0008527	OMIM:605472	IEA					P	HPO:iea[2009-02-17]
OMIM:615926	Webb-Dattani syndrome		HP:0002069	PMID:24022475	PCS		6/6			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0003158	PMID:24022475	PCS		5/5			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0010627	PMID:24022475	PCS		6/6			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0002188	PMID:24022475	PCS		6/6			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0002002	PMID:24022475	PCS		6/6			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0004322	PMID:24022475	PCS		3/5			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0002020	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0011220	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0000618	PMID:24022475	PCS		6/6			P	HPO:skoehler[2018-10-08]
OMIM:615926	Webb-Dattani syndrome		HP:0000873	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0003228	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0000278	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0003623	PMID:24022475	PCS		6/6			C	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0000011	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0000076	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0002079	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0011748	PMID:24022475	PCS		4/5			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0000490	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0005484	PMID:24022475	PCS		6/6			P	HPO:skoehler[2015-12-30]
OMIM:615926	Webb-Dattani syndrome		HP:0011344	PMID:24022475	PCS		6/6			P	HPO:skoehler[2019-09-07]
OMIM:615926	Webb-Dattani syndrome		HP:0002827	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0000007	PMID:24022475	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0008245	PMID:24022475	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0000824	PMID:24022475	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0001257	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24]
OMIM:615926	Webb-Dattani syndrome		HP:0000028	PMID:24022475	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0001513	PMID:24022475	PCS		4/6			P	HPO:probinson[2023-05-21]
OMIM:615926	Webb-Dattani syndrome		HP:0000126	PMID:24022475	PCS		6/6			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-05-21]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0002223	OMIM:182815	IEA					P	HPO:iea[2009-02-17]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0000561	OMIM:182815	IEA					P	HPO:iea[2012-03-02]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0003693	OMIM:182815	IEA					P	HPO:iea[2009-02-17]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0003383	OMIM:182815	IEA					P	HPO:iea[2009-02-17]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0007220	OMIM:182815	PCS					P	HPO:probinson[2012-03-12]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0011402	OMIM:182815	PCS					P	HPO:probinson[2012-03-12]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0001258	OMIM:182815	IEA					P	HPO:iea[2009-02-17]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0000006	OMIM:182815	IEA					I	HPO:iea[2009-02-17]
OMIM:182815	Spastic paraplegia with neuropathy and poikiloderma		HP:0001029	OMIM:182815	IEA					P	HPO:iea[2009-02-17]
OMIM:620745	Deafness, autosomal recessive 123		HP:0001751	PMID:36355422	PCS		0/8			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:620745	Deafness, autosomal recessive 123		HP:0000407	PMID:36355422	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:620745	Deafness, autosomal recessive 123		HP:0000007	PMID:36355422	PCS					I	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:620745	Deafness, autosomal recessive 123		HP:0000256	PMID:36355422	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:620745	Deafness, autosomal recessive 123		HP:0001249	PMID:36355422	PCS		0/8			P	ORCID:0000-0002-0736-9199[2024-05-20]
OMIM:212500	Cataract 46, juvenile-onset		HP:0000007	PMID:26788539	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:212500	Cataract 46, juvenile-onset		HP:0001118	PMID:26788539	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-03]
OMIM:212500	Cataract 46, juvenile-onset		HP:0011675	PMID:26788539	PCS		14/19			P	HPO:probinson[2021-07-03]
OMIM:212500	Cataract 46, juvenile-onset		HP:0001645	PMID:26788539	PCS	HP:0003581	5/19			P	HPO:probinson[2021-07-03]
OMIM:265950	Pyloric atresia		HP:0001561	OMIM:265950	IEA					P	HPO:iea[2009-02-17]
OMIM:265950	Pyloric atresia		HP:0004399	OMIM:265950	IEA					P	HPO:iea[2009-02-17]
OMIM:265950	Pyloric atresia		HP:0000007	OMIM:265950	IEA					I	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0002664	OMIM:310465	IEA					P	HPO:skoehler[2010-06-18]
OMIM:310465	N syndrome		HP:0000365	OMIM:310465	IEA					P	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0001909	OMIM:310465	TAS					P	HPO:skoehler[2009-02-17]
OMIM:310465	N syndrome		HP:0003220	OMIM:310465	IEA					P	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0000505	OMIM:310465	IEA					P	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0001417	OMIM:310465	IEA					I	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0000047	OMIM:310465	IEA					P	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0001257	OMIM:310465	IEA					P	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0000028	OMIM:310465	IEA					P	HPO:iea[2009-02-17]
OMIM:310465	N syndrome		HP:0001249	OMIM:310465	IEA					P	HPO:iea[2009-02-17]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0001276	PMID:35202461	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0002540	PMID:35202461	PCS		5/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0004322	PMID:35202461	PCS		4/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0002063	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0003593	PMID:35202461	PCS		4/6			C	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0033725	PMID:35202461	PCS		1/5			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000639	PMID:35202461	PCS		3/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0011463	PMID:35202461	PCS		2/6			C	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0100704	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000718	PMID:35202461	PCS		3/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0003429	PMID:35202461	PCS		2/5			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000218	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000752	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0001347	PMID:35202461	PCS		5/5			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000252	PMID:35202461	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0001344	PMID:35202461	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0002650	PMID:35202461	PCS		3/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0001266	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0011968	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0002194	PMID:35202461	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0011344	PMID:35202461	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0100660	PMID:35202461	PCS		2/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000729	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000007	PMID:35202461	PCS					I	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0200134	PMID:35202461	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0100716	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:620023	Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures		HP:0000787	PMID:35202461	PCS		1/6			P	HPO:probinson[2022-10-07]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0001252	PMID:17704778	PCS		3/11			P	HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0011463	PMID:17704778	PCS		2/4			C	HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0011220	PMID:17704778	PCS		2/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0012450	PMID:17704778	PCS		2/11			P	HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000218	PMID:17704778	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000774	PMID:17704778	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000256	PMID:17704778	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0001249	PMID:17704778	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0003623	PMID:17704778	PCS		2/4			C	HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000275	PMID:17704778	PCS		7/11			P	HPO:probinson[2012-05-01];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000098	PMID:17704778	PCS		2/11			P	HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0002650	PMID:17704778	PCS		3/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000276	PMID:17704778	PCS		6/11			P	HPO:probinson[2012-05-01];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0011302	PMID:17704778	PCS		3/11			P	HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0002808	PMID:17704778	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0001419	PMID:17704778	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000729	PMID:17704778	PCS		4/8			P	HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000327	PMID:17704778	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000767	PMID:17704778	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000426	PMID:17704778	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0001833	PMID:17704778	PCS		1/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000768	PMID:17704778	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0001533	PMID:17704778	PCS		7/11			P	HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0000303	PMID:17704778	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:300676	Intellectual developmental disorder, X-linked syndromic 14		HP:0001611	PMID:17704778	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-26]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0002223	OMIM:200110	PCS					P	HPO:iea[2012-02-21]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000561	PMID:26119818	PCS		2/10			P	HPO:iea[2012-02-21];HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001770	OMIM:200110	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0003577	PMID:26119818	PCS		9/10			C	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000365	PMID:26119818	PCS		3/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000188	OMIM:200110	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000062	PMID:26119818	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001195	PMID:26119818	PCS		1/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0010049	OMIM:200110	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0010669	PMID:26119818	PCS		1/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0008070	PMID:26119818	PCS		9/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0034260	PMID:26119818	PCS		2/10			P	HPO:probinson[2022-09-05]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0034262	PMID:26119818	PCS		6/10			P	HPO:probinson[2022-06-04]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000958	OMIM:200110	IEA					P	HPO:iea[2009-02-17]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0011266	PMID:26119818	PCS		10/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001804	PMID:26119818	PCS		1/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0011461	PMID:26119818	PCS		1/10			C	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000316	OMIM:200110;PMID:26119818	PCS		12/20			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0002933	OMIM:200110	PCS					P	HPO:iea[2012-03-02]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001126	OMIM:200110	IEA					P	HPO:iea[2009-02-17]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0002557	PMID:26119818	PCS		4/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000059	PMID:26119818	PCS		4/5	FEMALE		P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001545	PMID:26119818	PCS		3/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000154	PMID:26119818	PCS		9/10			P	HPO:iea[2012-03-02];HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0005105	OMIM:200110	PCS					P	HPO:iea[2012-03-02]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000054	PMID:26119818	PCS		1/5	FEMALE		P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000750	PMID:26119818	PCS		2/10			P	HPO:iea[2012-03-02];HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001762	OMIM:200110	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001582	PMID:26119818	PCS		4/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0010554	PMID:26119818	PCS		4/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0011224	PMID:26119818	PCS		6/10			P	HPO:skoehler[2013-05-29];HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0011267	OMIM:200110	IEA					P	HPO:iea[2009-02-17]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0012385	PMID:26119818	PCS		4/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0100678	PMID:26119818	PCS		5/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0001539	PMID:26119818	PCS		3/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0004209	PMID:26119818	PCS		1/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000006	PMID:26119818	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000369	PMID:26119818	PCS		4/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0000963	PMID:26119818	PCS		6/10			P	HPO:probinson[2022-05-07]
OMIM:200110	Ablepharon-Macrostomia syndrome		HP:0430009	PMID:26119818	PCS		3/12			P	HPO:probinson[2022-05-07]
OMIM:309120	Spermatogenic failure, X-linked 2		HP:0001419	PMID:25970010	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-22]
OMIM:309120	Spermatogenic failure, X-linked 2		HP:0003251	PMID:25970010	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:309120	Spermatogenic failure, X-linked 2		HP:0011462	PMID:25970010	PCS		7/7			C	HPO:probinson[2023-02-22]
OMIM:309120	Spermatogenic failure, X-linked 2		HP:0000029	PMID:25970010	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:309120	Spermatogenic failure, X-linked 2		HP:0031038	PMID:25970010	PCS		5/5			P	HPO:probinson[2023-02-22]
OMIM:309120	Spermatogenic failure, X-linked 2		HP:0000027	PMID:25970010	PCS		7/7			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-02-22]
OMIM:607488	Dystonia 15, myoclonic		HP:0002356	OMIM:607488	IEA					P	HPO:iea[2009-02-17]
OMIM:607488	Dystonia 15, myoclonic		HP:0001332	OMIM:607488	TAS					P	HPO:probinson[2012-07-16]
OMIM:607488	Dystonia 15, myoclonic		HP:0000006	OMIM:607488	IEA					I	HPO:iea[2009-02-17]
OMIM:607488	Dystonia 15, myoclonic		HP:0001336	OMIM:607488	IEA					P	HPO:iea[2009-02-17]
OMIM:168200	Paramolar tubercle of bolk		HP:0000164	OMIM:168200	IEA					P	HPO:iea[2009-02-17]
OMIM:168200	Paramolar tubercle of bolk		HP:0000006	OMIM:168200	IEA					I	HPO:iea[2009-02-17]
OMIM:312500	Reticuloendotheliosis, X-linked		HP:0001903	OMIM:312500	IEA					P	HPO:iea[2009-02-17]
OMIM:312500	Reticuloendotheliosis, X-linked		HP:0003593	OMIM:312500	IEA					C	HPO:iea[2009-02-17]
OMIM:312500	Reticuloendotheliosis, X-linked		HP:0002716	OMIM:312500	IEA					P	HPO:iea[2009-02-17]
OMIM:312500	Reticuloendotheliosis, X-linked		HP:0001417	OMIM:312500	IEA					I	HPO:iea[2009-02-17]
OMIM:312500	Reticuloendotheliosis, X-linked		HP:0001433	OMIM:312500	IEA					P	HPO:iea[2009-02-17]
OMIM:312500	Reticuloendotheliosis, X-linked		HP:0000952	OMIM:312500	IEA					P	HPO:iea[2009-02-17]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0001320	PMID:37226891	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0000252	PMID:37226891	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0003577	PMID:37226891	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0000750	PMID:37226891	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0001250	PMID:37226891	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0001263	PMID:37226891	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0003593	PMID:37226891	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0001270	PMID:37226891	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0000718	PMID:37226891	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0000717	PMID:37226891	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0000007	PMID:37226891	PCS					I	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0007018	PMID:37226891	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0001510	PMID:37226891	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0001249	PMID:37226891	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:620779	Intellectual developmental disorder, autosomal recessive 82		HP:0000369	PMID:37226891	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:612913	Orofaciodigital syndrome XI		HP:0002751	OMIM:612913	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612913	Orofaciodigital syndrome XI		HP:0100259	PMID:25876182	PCS	HP:0003577	1/1			P	HPO:probinson[2020-09-06];HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0000175	PMID:7531942	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0000494	PMID:25876182	PCS		1/1			P	HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0000431	PMID:25876182	PCS		1/1			P	HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0003311	PMID:25876182	PCS		1/1			P	HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0001250	PMID:25876182	PCS	HP:0003593	1/1			P	HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0002020	PMID:25876182	PCS		1/1			P	HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0000414	PMID:25876182	PCS		1/1			P	HPO:probinson[2020-09-06]
OMIM:612913	Orofaciodigital syndrome XI		HP:0003745	OMIM:612913	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612913	Orofaciodigital syndrome XI		HP:0001249	PMID:7531942	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2020-09-06]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0005425	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0001045	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0004313	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0005424	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0030388	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0011463	PMID:32484799	PCS		1/1			C	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0002729	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0000007	PMID:32484799	PCS					I	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0001888	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0002716	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0001973	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619846	Immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias		HP:0001510	PMID:32484799	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:606966	Nephronophthisis 4		HP:0003774	OMIM:606966	IEA					P	HPO:iea[2009-02-17]
OMIM:606966	Nephronophthisis 4		HP:0005576	OMIM:606966	TAS					P	HPO:probinson[2009-02-17]
OMIM:606966	Nephronophthisis 4		HP:0001959	OMIM:606966	IEA					P	HPO:iea[2009-02-17]
OMIM:606966	Nephronophthisis 4		HP:0001903	OMIM:606966	IEA					P	HPO:iea[2009-02-17]
OMIM:606966	Nephronophthisis 4		HP:0000007	OMIM:606966	IEA					I	HPO:iea[2009-02-17]
OMIM:606966	Nephronophthisis 4		HP:0000090	OMIM:606966	IEA					P	HPO:iea[2009-02-17]
OMIM:606966	Nephronophthisis 4		HP:0000108	OMIM:606966	IEA					P	HPO:iea[2011-12-31]
OMIM:606966	Nephronophthisis 4		HP:0000092	OMIM:606966	IEA					P	HPO:iea[2011-12-31]
OMIM:606966	Nephronophthisis 4		HP:0000103	OMIM:606966	IEA					P	HPO:iea[2009-02-17]
OMIM:606966	Nephronophthisis 4		HP:0001510	OMIM:606966	IEA					P	HPO:iea[2009-02-17]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0003477	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000341	PMID:31256876	PCS		1/9			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001199	PMID:31256876	PCS		3/14			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0010804	PMID:31256876	PCS		2/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001792	PMID:31256876	PCS		5/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000582	PMID:31256876	PCS		1/9			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000365	PMID:31256876	PCS		7/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000343	PMID:31256876	PCS		3/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001250	PMID:31256876	PCS	HP:0003593	14/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0003155	PMID:31256876	PCS		8/9			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0010808	PMID:31256876	PCS		2/9			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001290	PMID:31256876	PCS		7/8			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000280	PMID:31256876	PCS		4/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0012402	PMID:31256876	PCS		2/14			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0007141	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001508	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000319	PMID:31256876	PCS		2/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0009882	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000316	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0002119	PMID:31256876	PCS		2/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000218	PMID:31256876	PCS		2/9			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001522	PMID:31256876	PCS					C	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000377	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000358	PMID:31256876	PCS		2/9			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001265	PMID:31256876	PCS		1/11			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000154	PMID:31256876	PCS		1/9			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000396	PMID:31256876	PCS		3/9			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001762	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000431	PMID:31256876	PCS		2/9			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0002079	PMID:31256876	PCS		3/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000293	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0011968	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001263	PMID:31256876	PCS		12/12			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0009909	PMID:31256876	PCS		5/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001284	PMID:31256876	PCS		2/11			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001182	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000007	PMID:31256876	PCS					I	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0025404	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000307	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000505	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000543	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0001510	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000520	PMID:31256876	PCS		1/9			P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0002126	PMID:31256876	PCS		2/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0002500	PMID:31256876	PCS					P	HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000369	PMID:31256876	PCS		3/14			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618580	Epileptic encephalopathy, early infantile, 80		HP:0000347	PMID:31256876	PCS		3/9			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0002751	PMID:22814392	PCS		1/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0002510	PMID:22814392	PCS		1/2			P	HPO:probinson[2021-09-26];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0001344	PMID:22814392	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0001640	PMID:22814392	PCS	HP:0003596	2/2			P	HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0001250	PMID:22814392	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0001263	PMID:22814392	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0000053	PMID:22814392	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0001419	PMID:22814392	PCS					I	HPO:skoehler[2012-12-30];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0000238	PMID:22814392	PCS		1/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0001635	PMID:22814392	PCS	HP:0003596	2/2			P	HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0000400	PMID:22814392	PCS		2/2			P	HPO:skoehler[2012-12-30];HPO:probinson[2021-09-26]
OMIM:300886	Intellectual developmental disorder, X-linked, syndromic 32		HP:0000256	PMID:22814392	PCS		1/2			P	HPO:probinson[2021-09-26]
OMIM:618594	Nephrotic syndrome, type 21		HP:0003774	PMID:29058690	PCS	HP:0011463	2/2			P	HPO:probinson[2020-07-17]
OMIM:618594	Nephrotic syndrome, type 21		HP:0000007	PMID:29058690	PCS					I	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618594	Nephrotic syndrome, type 21		HP:0031266	PMID:29058690	PCS					P	HPO:probinson[2020-07-17]
OMIM:618594	Nephrotic syndrome, type 21		HP:0001967	PMID:29058690	PCS		2/2			P	HPO:probinson[2020-07-17]
OMIM:618594	Nephrotic syndrome, type 21		HP:0012588	PMID:29058690	PCS	HP:0003593	2/2			P	HPO:probinson[2020-07-17]
OMIM:260800	Pentosuria		HP:0025742	PMID:22042873	PCS					P	HPO:probinson[2024-08-03];HPO:probinson[2024-08-03]
OMIM:260800	Pentosuria		HP:0000007	PMID:22042873	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-08-03]
OMIM:276904	Usher syndrome, type IC		HP:0000007	OMIM:276904	IEA					I	HPO:iea[2009-02-17]
OMIM:276904	Usher syndrome, type IC		HP:0001756	OMIM:276904	IEA					P	HPO:iea[2009-02-17]
OMIM:276904	Usher syndrome, type IC		HP:0000510	OMIM:276904	IEA					P	HPO:iea[2009-02-17]
OMIM:276904	Usher syndrome, type IC		HP:0008527	OMIM:276904	TAS				HP:0012829	P	HPO:probinson[2009-02-17]
OMIM:618219	Polydactyly, postaxial, type A9		HP:0001162	PMID:30395363	PCS		3/3			P	HP:probinson[2019-04-19];HP:probinson[2019-04-19]
OMIM:618219	Polydactyly, postaxial, type A9		HP:0000007	PMID:30395363	PCS					I	HPO:skoehler[2019-04-18];HP:probinson[2019-04-19]
OMIM:618219	Polydactyly, postaxial, type A9		HP:0001830	PMID:30395363	PCS		1/3			P	HP:probinson[2019-04-19];HP:probinson[2019-04-19]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000486	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0031627	PMID:38480682	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0001332	PMID:38480682	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0008948	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0004322	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0001250	PMID:38480682	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0001252	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0001251	PMID:38480682	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0003593	PMID:38480682	PCS		6/10			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0001270	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000716	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0011462	PMID:38480682	PCS		4/10			C	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000739	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000519	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000733	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000218	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002857	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0007346	PMID:38480682	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000256	PMID:38480682	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0007229	PMID:38480682	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002135	PMID:38480682	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000252	PMID:38480682	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002015	PMID:38480682	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0001300	PMID:38480682	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002076	PMID:38480682	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002273	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0001680	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002072	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002071	PMID:38480682	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000709	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0034295	PMID:38480682	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0010780	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0007352	PMID:38480682	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0007256	PMID:38480682	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000007	PMID:38480682	PCS					I	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0007874	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002425	PMID:38480682	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000520	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0007018	PMID:38480682	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0002126	PMID:38480682	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:620786	Basal ganglia calcification, idiopathic, 9, autosomal recessive		HP:0000369	PMID:38480682	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-22]
OMIM:226100	Endocardial fibroelastosis and coarctation of abdominal aorta		HP:0004974	OMIM:226100	IEA					P	HPO:iea[2009-02-17]
OMIM:226100	Endocardial fibroelastosis and coarctation of abdominal aorta		HP:0001706	OMIM:226100	IEA					P	HPO:iea[2009-02-17]
OMIM:226100	Endocardial fibroelastosis and coarctation of abdominal aorta		HP:0000007	OMIM:226100	IEA					I	HPO:iea[2009-02-17]
OMIM:226100	Endocardial fibroelastosis and coarctation of abdominal aorta		HP:0001638	OMIM:226100	IEA					P	HPO:iea[2009-02-17]
OMIM:226100	Endocardial fibroelastosis and coarctation of abdominal aorta		HP:0001653	OMIM:226100	IEA					P	HPO:iea[2009-02-17]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000143	OMIM:270420	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0001561	PMID:19185281	PCS		5/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000175	PMID:19185281	PCS		1/22			P	HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0002023	PMID:19185281	PCS		2/16			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000453	PMID:19185281	PCS		10/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000073	OMIM:270420	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000075	PMID:19185281	PCS		1/22			P	HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0003270	OMIM:270420	IEA					P	HPO:iea[2009-02-17]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000316	PMID:19185281	PCS		3/22			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000007	PMID:19185281	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000256	OMIM:270420	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0005208	PMID:19185281	PCS		22/22			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0200020	PMID:19185281	PCS		9/22			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0002566	OMIM:270420	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000369	OMIM:270420	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000973	OMIM:270420	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:270420	Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies		HP:0000588	OMIM:270420	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:614345	Intellectual developmental disorder, autosomal recessive 24		HP:0000252	OMIM:614345	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614345	Intellectual developmental disorder, autosomal recessive 24		HP:0000750	OMIM:614345	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614345	Intellectual developmental disorder, autosomal recessive 24		HP:0000007	OMIM:614345	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614345	Intellectual developmental disorder, autosomal recessive 24		HP:0001270	OMIM:614345	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614345	Intellectual developmental disorder, autosomal recessive 24		HP:0001510	OMIM:614345	TAS					P	HPO:skoehler[2017-07-13]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0001332	PMID:31775912	PCS		1/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0001288	PMID:31775912	PCS		2/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0002352	PMID:31775912	PCS		1/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0002063	PMID:31775912	PCS		2/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0003581	PMID:31775912	PCS		2/2			C	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0010871	PMID:31775912	PCS		1/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0030903	PMID:31775912	PCS		1/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0031358	PMID:31775912	PCS		2/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0012377	PMID:31775912	PCS		1/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0000726	PMID:31775912	PCS		2/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0012196	PMID:31775912	PCS		1/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0000751	PMID:31775912	PCS		1/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0001268	PMID:31775912	PCS		2/2			P	HPO:probinson[2022-03-23]
OMIM:619661	Leukoencephalopathy, hereditary diffuse, with spheroids 2		HP:0000006	PMID:31775912	PCS					I	HPO:probinson[2022-03-23]
OMIM:222400	Diaphragmatic hernia 2		HP:0000007	OMIM:222400	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:222400	Diaphragmatic hernia 2		HP:0001426	OMIM:222400	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:222400	Diaphragmatic hernia 2		HP:0008986	OMIM:222400	IEA					P	HPO:iea[2009-02-17]
OMIM:222400	Diaphragmatic hernia 2		HP:0000776	OMIM:222400	IEA					P	HPO:skoehler[2015-01-27]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002323	PMID:26166481	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002983	PMID:26166481	PCS		3/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0003577	PMID:26166481	PCS		8/8			C	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002089	OMIM:616546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002365	PMID:26166481	PCS		2/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000480	PMID:26166481	PCS		2/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0001290	OMIM:616546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002280	PMID:26166481	PCS		1/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000238	PMID:26166481	PCS		2/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0001789	PMID:26166481	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002419	PMID:26166481	PCS		5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002119	PMID:26166481	PCS		1/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000774	OMIM:616546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002436	PMID:26166481	PCS		3/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000773	PMID:26166481	PCS		4/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000113	PMID:26166481	PCS		0/6			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000776	PMID:26166481	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0001320	PMID:26166481	PCS		4/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0001265	OMIM:616546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000175	OMIM:616546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000054	PMID:26166481	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0001561	OMIM:616546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002079	PMID:26166481	PCS		3/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000470	PMID:26166481	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0032466	PMID:26166481	PCS		1/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0011802	PMID:26166481	PCS		1/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000191	PMID:26166481	PCS		2/8			P	HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0005280	PMID:26166481	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0100259	PMID:26166481	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0100258	PMID:26166481	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0006660	PMID:26166481	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000007	PMID:26166481	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0001631	OMIM:616546	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0000369	PMID:26166481	PCS		1/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		HP:0002126	PMID:26166481	PCS		3/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0005689	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0002652	OMIM:211960	IEA					P	HPO:skoehler[2015-12-30]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0003236	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0000343	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0001762	OMIM:211960	TAS					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0001245	OMIM:211960	TAS					P	HPO:probinson[2012-06-10]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0000023	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0010487	OMIM:211960	TAS					P	HPO:probinson[2012-06-10]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0012385	OMIM:211960	TAS					P	HPO:skoehler[2013-10-22]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0009473	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0000316	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0000007	OMIM:211960	IEA					I	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0007477	OMIM:211960	TAS					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0002414	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0001634	OMIM:211960	IEA					P	HPO:iea[2009-02-17]
OMIM:211960	Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormalpalmar creases		HP:0003457	OMIM:211960	TAS					P	HPO:skoehler[2012-10-17]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0003596	PMID:10580070	PCS		10/40			C	HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0011705	PMID:10580070	PCS		1/40			P	HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0011706	PMID:10580070	PCS		3/40			P	HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0005110	PMID:10580070	PCS		19/40			P	HPO:probinson[2012-04-11];HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0001709	PMID:10580070	PCS		5/40			P	HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0011462	PMID:10580070	PCS		20/40			C	HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0001635	PMID:10580070	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0004749	OMIM:115200	PCS					P	HPO:probinson[2012-04-11]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0004308	OMIM:115200	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2012-04-11]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0001698	OMIM:115200	PCS					P	HPO:probinson[2012-04-11]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0000006	PMID:10580070	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0001645	PMID:10580070	PCS		9/40			P	HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0001644	PMID:10580070	PCS		27/40			P	HPO:probinson[2012-04-11];HPO:probinson[2021-09-06]
OMIM:115200	Cardiomyopathy, dilated, 1A		HP:0001688	PMID:10580070	PCS		4/40			P	HPO:probinson[2021-09-06]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0001297	PMID:20389311	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0010648	PMID:16685658	PCS		1/1			P	HPO:probinson[2023-03-27]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0005133	PMID:17937443	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0001252	PMID:16685658	PCS		1/1			P	HPO:skoehler[2014-11-26]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0010444	OMIM:614437	TAS					P	HPO:probinson[2013-08-10]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0011220	OMIM:614437	TAS					P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000316	OMIM:614437;PMID:20389311	PCS		12/13			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0002616	PMID:16685658	PCS		1/1			P	HPO:probinson[2023-03-27];HPO:probinson[2023-03-27]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0100807	PMID:20389311	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0002414	PMID:19664000	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000278	PMID:20389311	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0004955	PMID:16685658	PCS		1/1			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000252	OMIM:614437	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000494	OMIM:614437	TAS					P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0010759	OMIM:614437	TAS					P	HPO:probinson[2013-08-10]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0001662	PMID:19664000	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0001382	PMID:20389311	PCS		1/3			P	HPO:probinson[2013-08-10]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0004970	PMID:17937443	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0005180	PMID:17937443	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0100699	PMID:20389311	PCS		0/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0004927	OMIM:614437	TAS					P	HPO:probinson[2013-08-10]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000767	PMID:16685658	PCS		1/1			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000007	PMID:16685658	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-03-27]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000444	PMID:19664000	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000520	OMIM:614437	TAS					P	HPO:probinson[2013-08-10]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000369	OMIM:614437	TAS					P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0003577	PMID:16685658;PMID:17937443	PCS		2/2			C	HPO:probinson[2023-03-27];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0005116	PMID:16685658;PMID:20389311	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000023	PMID:16685658	PCS		1/1			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0012368	PMID:20389311	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0001548	OMIM:614437	TAS		1/1			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0004937	OMIM:614437	TAS					P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000414	OMIM:614437	TAS					P	HPO:probinson[2013-08-10]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000977	PMID:16685658;PMID:20389311	PCS		2/4			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000218	OMIM:614437;PMID:20389311	PCS		11/13			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000377	PMID:19664000	PCS		1/1			P	HPO:skoehler[2013-08-18];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000776	PMID:16685658	PCS		1/1			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000973	PMID:16685658;PMID:19664000;PMID:17937443	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0001562	PMID:16685658;PMID:19664000	PCS		2/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2023-03-27];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0001166	OMIM:614437;PMID:19664000	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2023-03-27];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0002576	PMID:17937443	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0002097	PMID:16685658	PCS		1/1			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0045025	OMIM:614437	TAS		1/1			P	HPO:skoehler[2014-11-27]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0002092	PMID:17937443	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0005280	OMIM:614437	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0040044	PMID:19664000	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0003819	PMID:20389311	PCS		1/3			C	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0004948	PMID:16685658;PMID:19664000	PCS		2/2			P	HPO:probinson[2023-03-27];HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0006487	PMID:19664000	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0003811	PMID:19664000;PMID:17937443	PCS		2/2			C	HPO:probinson[2024-03-15]
OMIM:614437	Cutis laxa, autosomal recessive, type IB		HP:0000347	OMIM:614437	TAS		1/1			P	HPO:probinson[2013-08-10]
OMIM:191100	Tuberous sclerosis-1		HP:0009717	PMID:29196670	PCS		4/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0009716	PMID:29196670	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0009719	PMID:29196670	PCS		2/5			P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0001250	PMID:29196670	PCS		4/5			P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0010762	OMIM:191100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:191100	Tuberous sclerosis-1		HP:0012469	PMID:14985384	PCS		3/22			P	HPO:skoehler[2013-11-28];HPO:probinson[2019-10-10]
OMIM:191100	Tuberous sclerosis-1		HP:0000957	OMIM:191100	TAS					P	HPO:skoehler[2014-06-24]
OMIM:191100	Tuberous sclerosis-1		HP:0000717	PMID:14985384	PCS		3/22			P	HPO:iea[2009-02-17];HPO:probinson[2019-10-10]
OMIM:191100	Tuberous sclerosis-1		HP:0009720	OMIM:191100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0001328	OMIM:191100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:191100	Tuberous sclerosis-1		HP:0006772	PMID:14985384;PMID:29196670	PCS		12/15			P	HPO:iea[2009-02-17];HPO:probinson[2019-10-10];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0009722	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0200024	OMIM:191100	IEA					P	HPO:skoehler[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0009721	PMID:29196670	PCS		1/5			P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0009724	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0002514	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0007206	PMID:22497611	PCS					P	HPO:lccarmody[2018-10-25];HPO:lccarmody[2018-10-25]
OMIM:191100	Tuberous sclerosis-1		HP:0001249	PMID:14985384;PMID:29196670	PCS		6/27			P	HPO:skoehler[2012-11-18];HPO:probinson[2019-10-10];ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0009727	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0010615	PMID:29196670	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0009729	OMIM:191100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0005584	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0001482	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0012798	PMID:10852420	PCS		20/78	FEMALE		P	HPO:probinson[2019-11-28]
OMIM:191100	Tuberous sclerosis-1		HP:0012798	PMID:16485546	PCS		HP:0040284	MALE		P	HPO:probinson[2019-11-28]
OMIM:191100	Tuberous sclerosis-1		HP:0012798	PMID:29196670	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0011097	PMID:26067126	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2019-11-28]
OMIM:191100	Tuberous sclerosis-1		HP:0009592	OMIM:191100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:191100	Tuberous sclerosis-1		HP:0000826	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0009594	PMID:29196670	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0001716	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0000729	PMID:29196670	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-06-06]
OMIM:191100	Tuberous sclerosis-1		HP:0000107	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0000821	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0009554	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0000169	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0007018	OMIM:191100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:191100	Tuberous sclerosis-1		HP:0002888	OMIM:191100	IEA					P	HPO:iea[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0009734	OMIM:191100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:191100	Tuberous sclerosis-1		HP:0000006	PMID:14985384	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-10-10]
OMIM:619113	COACH syndrome 3		HP:0032945	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0003774	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000486	PMID:19574260	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0032948	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000083	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0001263	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0001251	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0003593	PMID:19574260	IEA		2/2			C	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0001290	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000090	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000092	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0006580	PMID:19574260	PCS		1/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0001903	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000729	PMID:19574260	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000508	PMID:19574260	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000657	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0000007	PMID:19574260	PCS					I	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619113	COACH syndrome 3		HP:0002419	PMID:19574260	PCS		2/2			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:616220	Focal segmental glomerulosclerosis 9		HP:0003621	PMID:25557779	PCS		1/4			C	HPO:probinson[2022-11-08]
OMIM:616220	Focal segmental glomerulosclerosis 9		HP:0011463	PMID:25557779	PCS		2/4			C	HPO:probinson[2022-11-08]
OMIM:616220	Focal segmental glomerulosclerosis 9		HP:0000097	PMID:25557779	PCS		4/4			P	HPO:skoehler[2015-03-22];HPO:probinson[2022-11-08]
OMIM:616220	Focal segmental glomerulosclerosis 9		HP:0003593	PMID:25557779	PCS		1/4			C	HPO:probinson[2022-11-08]
OMIM:616220	Focal segmental glomerulosclerosis 9		HP:0000007	PMID:25557779	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:616220	Focal segmental glomerulosclerosis 9		HP:0012588	PMID:25557779	PCS		5/5			P	HPO:probinson[2022-11-08]
OMIM:620792	Otosclerosis 12		HP:0000362	PMID:37399313	PCS		4/4			P	HPO:probinson[2024-07-19]
OMIM:620792	Otosclerosis 12		HP:0000365	PMID:37399313	PCS		7/7			P	HPO:probinson[2024-07-19]
OMIM:620792	Otosclerosis 12		HP:0011463	PMID:37399313	PCS		1/7			C	HPO:probinson[2024-07-19]
OMIM:620792	Otosclerosis 12		HP:0003584	PMID:37399313	PCS		2/7			C	HPO:probinson[2024-07-19]
OMIM:620792	Otosclerosis 12		HP:0011462	PMID:37399313	PCS		4/7			C	HPO:probinson[2024-07-19]
OMIM:620792	Otosclerosis 12		HP:0000006	PMID:37399313	PCS					I	HPO:probinson[2024-07-19]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0002664	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0004322	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0001272	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000580	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0001251	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0012056	OMIM:610651	TAS					P	HPO:probinson[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000518	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0002119	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000135	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0005328	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0001249	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0001347	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0002135	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0003224	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000252	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000992	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0004334	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0006739	OMIM:610651	TAS					P	HPO:probinson[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0001480	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0002671	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0011400	OMIM:610651	TAS					P	HPO:probinson[2012-04-11]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000407	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000007	OMIM:610651	IEA					I	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000568	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000648	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:610651	Xeroderma pigmentosum, complementation group B		HP:0000762	OMIM:610651	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0002015	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0001762	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0000211	PMID:20949528	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-06]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0002002	OMIM:158300	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0004322	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0011968	OMIM:158300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0005684	OMIM:158300	IEA					P	HPO:skoehler[2015-01-21]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0010621	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0400000	OMIM:158300	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0002827	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0000508	OMIM:158300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0002804	OMIM:158300	IEA					P	HPO:skoehler[2015-01-27]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0000256	OMIM:158300	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0001840	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0000006	PMID:15282353	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0000347	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0000324	OMIM:158300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:158300	Arthrogryposis, distal, type 7		HP:0001765	OMIM:158300	IEA					P	HPO:iea[2009-02-17]
OMIM:613370	Maturity-onset diabetes of the young, type 10		HP:0000819	PMID:18162506	PCS					P	HPO:skoehler[2012-10-17]
OMIM:613370	Maturity-onset diabetes of the young, type 10		HP:0004904	PMID:18162506	PCS	HP:0003593				P	HPO:skoehler[2015-01-19]
OMIM:613370	Maturity-onset diabetes of the young, type 10		HP:0003074	PMID:18162506	PCS	HP:0003593				P	HPO:lccarmody[2018-06-29]
OMIM:613370	Maturity-onset diabetes of the young, type 10		HP:0001511	PMID:18162506	PCS	HP:0030674				P	HPO:lccarmody[2018-06-29]
OMIM:613370	Maturity-onset diabetes of the young, type 10		HP:0000006	PMID:18162506	PCS					I	HPO:skoehler[2012-10-17]
OMIM:613370	Maturity-onset diabetes of the young, type 10		HP:0001953	PMID:18162506	PCS	HP:0003593				P	HPO:lccarmody[2018-06-29]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0002960	OMIM:130080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0007517	OMIM:130080	IEA					P	HPO:skoehler[2010-06-18]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0034518	PMID:27745832	PCS		20/21			P	HPO:probinson[2023-01-27]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001058	OMIM:130080	IEA					P	HPO:iea[2009-02-17]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0002761	OMIM:130080	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000023	OMIM:130080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001030	PMID:27745832	PCS		24/32			P	HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001373	PMID:27745832	PCS		2/25			P	HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001075	OMIM:130080;PMID:27745832	PCS		21/36			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0030816	PMID:27745832	PCS		29/33			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0031368	OMIM:130080	IEA					P	HPO:skoehler[2018-10-08]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0034517	PMID:27745832	PCS		24/25			P	HPO:probinson[2023-01-27]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0002719	OMIM:130080	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001609	OMIM:130080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000978	PMID:27745832	PCS		29/31			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000977	OMIM:130080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000974	PMID:27745832	PCS		20/27			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001166	OMIM:130080	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0002036	PMID:27745832	PCS		1/20			P	HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0410027	OMIM:130080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000098	OMIM:130080	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0002650	PMID:27745832	PCS		9/27			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001382	PMID:27745832	PCS		11/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000592	OMIM:130080	IEA					P	HPO:iea[2009-02-17]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0006480	OMIM:130080	IEA					P	HPO:iea[2009-02-17]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0002829	PMID:27745832	PCS		10/24			P	HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000704	PMID:27745832	PCS		30/34			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001537	PMID:27745832	PCS		2/20			P	HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0001015	PMID:27745832	PCS		9/20			P	HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000006	PMID:27745832	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000963	OMIM:130080	IEA					P	HPO:iea[2009-02-17]
OMIM:130080	Ehlers-Danlos syndrome, periodontal type, 1		HP:0000225	PMID:27745832	PCS		24/28			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-15]
OMIM:616208	Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia		HP:0003596	PMID:25374358	PCS		3/8			C	HPO:probinson[2023-02-27]
OMIM:616208	Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia		HP:0002145	PMID:25374358	PCS		2/8			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-27]
OMIM:616208	Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia		HP:0003584	PMID:25374358	PCS		5/8			C	HPO:probinson[2023-02-27]
OMIM:616208	Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia		HP:0007354	PMID:25374358	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:616208	Amyotrophic lateral sclerosis 22 with or without frontotemporal dementia		HP:0000006	PMID:25374358	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-27]
OMIM:617116	Epilepsy, familial focal, with variable foci 2		HP:0001250	OMIM:617116	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617116	Epilepsy, familial focal, with variable foci 2		HP:0003829	OMIM:617116	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617116	Epilepsy, familial focal, with variable foci 2		HP:0032046	PMID:27173016	PCS	HP:0011463	1/2	FEMALE		P	HPO:nvasilevsky[2018-09-17]
OMIM:617116	Epilepsy, familial focal, with variable foci 2		HP:0000006	OMIM:617116	TAS					I	HPO:skoehler[2017-07-13]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001254	OMIM:618225	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0000486	PMID:10080174	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001250	OMIM:618225	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001252	PMID:10080174	PCS		3/3			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0003593	PMID:10080174	PCS		3/3			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001251	OMIM:618225	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0032794	PMID:10080174	PCS		3/3			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0012444	PMID:10080174	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0000618	PMID:10080174	PCS		1/1			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0000256	PMID:10080174	PCS		1/2			P	HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0002415	PMID:10080174	PCS		1/2			P	HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001942	OMIM:618225	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0002013	PMID:10080174	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0002376	PMID:10080174	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0003542	PMID:10080174	PCS		2/2			P	HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001263	PMID:10080174	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0002151	PMID:10080174	PCS		2/3			P	HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0002490	PMID:10080174	PCS		3/3			P	HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0011923	PMID:10080174	PCS		3/3			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0003819	PMID:10080174	PCS		1/3			C	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0000508	OMIM:618225	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0000602	OMIM:618225	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0000007	PMID:10080174	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001257	PMID:10080174	PCS		1/2			P	HPO:probinson[2022-11-26]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0002104	OMIM:618225	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618225	Mitochondrial complex I deficiency, nuclear type 4		HP:0001336	PMID:10080174	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-26]
OMIM:194050	Williams-Beuren syndrome		HP:0000121	PMID:20089974	PCS		10%			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001297	PMID:20089974	PCS		HP:0040284			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000486	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0004322	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000089	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000083	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0003196	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0002020	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0002141	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001290	OMIM:194050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:194050	Williams-Beuren syndrome		HP:0003072	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		15%			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0008770	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001609	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000635	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001605	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0002019	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0200021	ISBN-13:978-0721606156	PCS	HP:0003581	HP:0040282			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0009748	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0002311	PMID:20089974;OMIM:194050	PCS		15/20			P	HPO:iea[2010-04-29];HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000010	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0002035	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0005145	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0002150	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		30%			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0011800	OMIM:194050	TAS					P	HPO:skoehler[2015-11-15]
OMIM:194050	Williams-Beuren syndrome		HP:0010794	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-05-11]
OMIM:194050	Williams-Beuren syndrome		HP:0000407	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000805	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000767	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000646	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000403	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0004969	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0004209	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000125	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000006	PMID:20089974	PCS					I	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001699	PMID:20089974	PCS		HP:0040284			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000341	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0001792	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000343	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams;ISBN-13:978-0721606156	PCS		10/20			P	HPO:iea[2010-04-29];HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0000463	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000581	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0004381	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		75%			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0012210	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000739	PMID:20089974	PCS		80%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0012450	OMIM:194050	TAS					P	HPO:skoehler[2013-11-28]
OMIM:194050	Williams-Beuren syndrome		HP:0008872	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001822	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000736	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000977	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000455	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0000179	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000973	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0000076	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001321	PMID:20089974	PCS		15%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000194	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0002253	PMID:20089974	PCS	HP:0011462	30%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0010780	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0007099	PMID:20089974	PCS		10%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000629	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0007018	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001952	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000286	ISBN-13:978-0721606156	PCS	HP:0011463	HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0004764	PMID:20089974	PCS		20%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001531	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		70%			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0001371	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001252	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0002183	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001409	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001647	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0002216	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001642	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS	HP:0003593	HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001249	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001920	PMID:20089974	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0002974	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0002751	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000054	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001382	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000293	ISBN-13:978-0721606156	PCS	HP:0011463	HP:0040282			P	HPO:iea[2010-05-03]
OMIM:194050	Williams-Beuren syndrome		HP:0000691	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0012537	OMIM:194050	IEA					P	HPO:skoehler[2018-10-08]
OMIM:194050	Williams-Beuren syndrome		HP:0001537	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000689	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000601	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001653	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001136	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000023	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0010747	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000819	PMID:20089974	PCS	HP:0003581	75%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000939	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001629	PMID:20089974	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000539	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000938	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000015	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001347	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000272	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0005280	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0100000	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		50%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000708	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0008661	ISBN-13:978-0721606156	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0002608	PMID:20089974	PCS		HP:0040283			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0000668	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000822	PMID:20089974	PCS		50%			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0000821	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		10%			P	HPO:iea[2010-04-29]
OMIM:194050	Williams-Beuren syndrome		HP:0001511	OMIM:194050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001631	PMID:20089974	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001634	PMID:20089974	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194050	Williams-Beuren syndrome		HP:0001513	ISBN-13:978-0721606156	PCS	HP:0003581	HP:0040282			P	HPO:iea[2010-04-29]
OMIM:608988	Atrial fibrillation, familial, 2		HP:0003581	PMID:12782570	PCS					C	HPO:probinson[2022-07-10]
OMIM:608988	Atrial fibrillation, familial, 2		HP:0005110	PMID:12782570	PCS					P	HPO:probinson[2022-07-10]
OMIM:608988	Atrial fibrillation, familial, 2		HP:0000006	PMID:12782570	PCS					I	HPO:probinson[2022-07-10]
OMIM:300851	Intellectual developmental disorder, X-linked 92		HP:0004322	PMID:16385466	PCS		3/8			P	HPO:probinson[2013-02-17]
OMIM:300851	Intellectual developmental disorder, X-linked 92		HP:0001419	OMIM:300851	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300851	Intellectual developmental disorder, X-linked 92		HP:0000581	PMID:16385466	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300851	Intellectual developmental disorder, X-linked 92		HP:0001417	PMID:16385466	PCS					I	HPO:probinson[2013-01-09]
OMIM:300851	Intellectual developmental disorder, X-linked 92		HP:0011003	PMID:16385466	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300851	Intellectual developmental disorder, X-linked 92		HP:0008734	PMID:16385466	PCS		2/8			P	HPO:probinson[2013-02-17]
OMIM:300851	Intellectual developmental disorder, X-linked 92		HP:0001249	PMID:16385466	PCS					P	HPO:probinson[2013-02-17]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0001760	OMIM:605274	IEA					P	HPO:iea[2009-02-17]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0001155	PMID:26032025	PCS		0/3			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0003577	PMID:26032025	PCS		3/3			C	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0003038	PMID:26032025	PCS		1/3			P	HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0001476	OMIM:605274	IEA					P	HPO:iea[2009-02-17]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0005852	PMID:26032025	PCS		1/3			P	HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0004322	PMID:26032025	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0001772	PMID:26032025	PCS		1/3			P	HPO:probinson[2012-07-16]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0005773	PMID:26032025	PCS		1/3			P	HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0002990	PMID:26032025	PCS		2/3			P	HPO:probinson[2009-02-17]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0001263	PMID:26032025	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0003173	PMID:26032025	PCS		1/3			P	HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0003083	PMID:26032025	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0006390	PMID:26032025	PCS		1/3			P	HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0002827	PMID:26032025	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0009556	PMID:26032025	PCS		1/3			P	HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0005736	PMID:26032025	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0002558	PMID:26032025	PCS		1/3			P	HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0000006	PMID:26032025	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:605274	Mesomelic dysplasia, Savarirayan type		HP:0004987	PMID:26032025	PCS		2/3			P	HPO:probinson[2024-03-10]
OMIM:114650	Car factor deficiency		HP:0001892	OMIM:114650	TAS					P	HPO:probinson[2009-02-17]
OMIM:114650	Car factor deficiency		HP:0000006	OMIM:114650	IEA					I	HPO:iea[2009-02-17]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0001650	PMID:23261303	PCS		1/16			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0031417	PMID:23261303	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0001696	PMID:23261303	PCS		5/16			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0001651	PMID:23261303	PCS		1/16			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0000144	PMID:23261303	PCS		0/7			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0005301	PMID:23261303	PCS		1/16			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0002110	PMID:23261303	PCS		6/6			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0031245	PMID:23261303	PCS		14/15		HP:0011010	P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0002092	PMID:23261303	PCS		1/16			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0100750	PMID:23261303	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0011538	PMID:23261303	PCS		1/16			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0011108	PMID:23261303	PCS		9/16			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0200073	PMID:23261303	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0012265	PMID:23261303	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0012256	PMID:23261303	PCS		2/2			P	HPO:probinson[2013-04-07];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0001629	PMID:23261303	PCS		2/16			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0001719	PMID:23261303	PCS		1/16			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0000403	PMID:23261303	PCS		15/16			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0000007	PMID:23261303	PCS					I	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0006532	PMID:23261303	PCS		5/15			P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0002205	PMID:23261303	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0004415	PMID:23261303	PCS		1/16			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0002105	PMID:23261303	PCS		5/14			P	HPO:probinson[2023-05-21]
OMIM:615067	Ciliary dyskinesia, primary, 20		HP:0003623	PMID:23261303	PCS		16/16			C	HPO:probinson[2023-05-21]
OMIM:614379	Complement component 4B deficiency		HP:0001287	OMIM:614379	IEA					P	HPO:skoehler[2015-08-23]
OMIM:614379	Complement component 4B deficiency		HP:0002099	PMID:1401055	PCS	HP:0003593	1/1			P	HPO:probinson[2022-04-10]
OMIM:614379	Complement component 4B deficiency		HP:0003593	PMID:1401055	PCS		1/1			C	HPO:probinson[2022-04-10]
OMIM:614379	Complement component 4B deficiency		HP:0000403	PMID:1401055	PCS	HP:0011463	1/1			P	HPO:probinson[2022-04-10]
OMIM:614379	Complement component 4B deficiency		HP:0045044	PMID:1401055	PCS		1/1			P	HPO:skoehler[2015-08-24];HPO:probinson[2022-04-10]
OMIM:614379	Complement component 4B deficiency		HP:0006532	PMID:1401055	PCS	HP:0011463	1/1			P	HPO:probinson[2022-04-10]
OMIM:614379	Complement component 4B deficiency		HP:0200120	OMIM:614379	IEA					P	HPO:skoehler[2015-08-23]
OMIM:614379	Complement component 4B deficiency		HP:0011108	PMID:1401055	PCS	HP:0011463	1/1			P	HPO:probinson[2022-04-10]
OMIM:614379	Complement component 4B deficiency		HP:0002028	PMID:1401055	PCS	HP:0003593	1/1			P	HPO:probinson[2022-04-10]
OMIM:615073	Dystonia 25		HP:0000473	PMID:23222958	PCS					P	HPO:skoehler[2013-11-28];HPO:probinson[2022-12-10]
OMIM:615073	Dystonia 25		HP:0003621	PMID:23222958	PCS					C	HPO:probinson[2022-12-10]
OMIM:615073	Dystonia 25		HP:0001618	PMID:23222958	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-10]
OMIM:615073	Dystonia 25		HP:0002451	PMID:23222958	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-10]
OMIM:615073	Dystonia 25		HP:0003581	PMID:23222958	PCS					C	HPO:probinson[2022-12-10]
OMIM:615073	Dystonia 25		HP:0012049	PMID:23222958	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-10]
OMIM:615073	Dystonia 25		HP:0000006	PMID:23222958	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2022-12-10]
OMIM:615073	Dystonia 25		HP:0031008	PMID:23222958	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-10]
OMIM:250900	Methionine malabsorption syndrome		HP:0002014	OMIM:250900	IEA					P	HPO:iea[2009-02-17]
OMIM:250900	Methionine malabsorption syndrome		HP:0003355	OMIM:250900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:250900	Methionine malabsorption syndrome		HP:0001250	OMIM:250900	IEA					P	HPO:iea[2009-02-17]
OMIM:250900	Methionine malabsorption syndrome		HP:0011364	OMIM:250900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:250900	Methionine malabsorption syndrome		HP:0000635	OMIM:250900	IEA					P	HPO:iea[2009-02-17]
OMIM:250900	Methionine malabsorption syndrome		HP:0000007	OMIM:250900	IEA					I	HPO:iea[2009-02-17]
OMIM:250900	Methionine malabsorption syndrome		HP:0002789	OMIM:250900	IEA					P	HPO:iea[2009-02-17]
OMIM:250900	Methionine malabsorption syndrome		HP:0001249	OMIM:250900	IEA					P	HPO:iea[2009-02-17]
OMIM:250900	Methionine malabsorption syndrome		HP:0003612	OMIM:250900	IEA					P	HPO:iea[2009-02-17]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0001265	OMIM:613402	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0000253	PMID:23224214	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0003202	OMIM:613402	TAS					P	HPO:skoehler[2014-08-24]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0000252	PMID:20118933;PMID:23224214	PCS		13/13			P	HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0002079	PMID:20118933	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0001250	PMID:20118933	PCS	HP:0003593	11/11			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0001272	PMID:23224214	PCS		2/2			P	HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0001252	PMID:23224214	PCS	HP:0003621				P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0001263	PMID:20118933;PMID:23224214	PCS		13/13			P	HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0001251	PMID:23224214	PCS		2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0001270	PMID:23224214	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0000007	PMID:20118933	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0002119	PMID:20118933	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0000752	PMID:20118933;PMID:23224214	PCS		12/12			P	HPO:probinson[2020-12-14];HPO:skoehler[2012-10-17];HPO:probinson[2020-12-14]
OMIM:613402	Microcephaly, seizures, and developmental delay		HP:0009879	OMIM:613402	TAS					P	HPO:skoehler[2014-11-26]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0003676	PMID:28777931	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002540	PMID:28777931	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000486	PMID:28777931	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001332	PMID:28777931	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001272	PMID:28777931	PCS		1/6			P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001250	PMID:28777931	PCS		1/6			P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0012707	PMID:28777931	PCS		1/4			P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001252	PMID:28777931	PCS					P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002020	PMID:28777931	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000085	PMID:28777931	PCS		1/6			P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0003593	PMID:28777931	PCS		5/6			C	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000280	PMID:28777931	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000639	PMID:28777931	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001522	PMID:28777931	PCS		2/6			C	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002019	PMID:28777931	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000577	PMID:28777931	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001347	PMID:28777931	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0003128	PMID:28777931	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0003623	PMID:28777931	PCS		1/6			C	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002751	PMID:28777931	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002015	PMID:28777931	PCS		3/5			P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000252	PMID:28777931	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001344	PMID:28777931	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001266	PMID:28777931	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002376	PMID:28777931	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0011968	PMID:28777931	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001263	PMID:28777931	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002151	PMID:28777931	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0002490	PMID:28777931	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0010535	PMID:28777931	PCS		2/6			P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0034392	PMID:28777931	PCS		3/6			P	HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000508	PMID:28777931	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000007	PMID:28777931	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0000648	PMID:28777931	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001257	PMID:28777931	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-31]
OMIM:617664	Combined oxidative phosphorylation deficiency 32		HP:0001337	PMID:28777931	PCS		3/6			P	HPO:probinson[2022-10-31]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0000252	PMID:31032849;PMID:29961870	PCS		11/15			P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0002045	PMID:29422393	PCS	HP:0003623	1/1			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0002540	PMID:29961870	PCS					P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0002133	PMID:31032849	PCS		3/5			P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001250	PMID:29422393	PCS	HP:0003623	1/1			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001250	PMID:29961870	IEA	HP:0003593	1/1			P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001250	PMID:31032849	IEA	HP:0003593	5/5			P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001263	PMID:31032849	PCS		5/5			P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001252	PMID:31032849	PCS		3/5			P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0002072	PMID:29422393	PCS	HP:0003593	1/1			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001290	PMID:29961870	PCS					P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0100021	PMID:29961870	PCS					P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0011344	PMID:29422393	PCS	HP:0003593	1/1			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0100704	PMID:29961870	PCS					P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0000817	PMID:29422393	PCS	HP:0003593	1/1			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0000729	PMID:31032849	PCS		2/4			P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001319	PMID:29422393	PCS	HP:0003623	1/1			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0003429	PMID:29961870	PCS					P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0001257	PMID:29961870	PCS					P	HPO:probinson[2020-06-28]
OMIM:618557	Epileptic encephalopathy, early infantile, 78		HP:0000006	PMID:31032849	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0003621	PMID:33891002	PCS		2/8			C	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0007814	PMID:33891002	PCS		5/16			P	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0000552	PMID:33891002	PCS		15/15			P	HPO:probinson[2022-02-26];HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0000662	PMID:33891002	PCS		4/16			P	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0009916	PMID:33891002	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:6000367	PMID:33891002	PCS		5/16			P	HPO:probinson[2024-02-27]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0011003	PMID:33891002	PCS		5/16			P	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0030528	PMID:33891002	PCS		4/16			P	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0012511	PMID:33891002	PCS		3/16			P	HPO:probinson[2022-02-26];HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:6000769	PMID:33891002	PCS		9/16			P	HPO:probinson[2024-08-03]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0000518	PMID:33891002	PCS	HP:0003581	4/16			P	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0011463	PMID:33891002	PCS		6/8			C	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0000613	PMID:33891002	PCS					P	HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0007663	PMID:33891002	PCS		15/16			P	HPO:probinson[2022-02-26];HPO:probinson[2022-02-26]
OMIM:619649	Chromosome 16q12 duplication syndrome		HP:0000006	PMID:33891002	PCS					I	HPO:probinson[2022-02-26]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000343	PMID:21596366	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0004322	PMID:21596366	PCS		7/7			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0001250	OMIM:300845	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0011834	PMID:21596366	PCS		6/7			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0031103	PMID:21596366	PCS		1/3			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000518	PMID:21596366	PCS	HP:0011463	4/7			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000815	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0008232	PMID:21596366	PCS		6/7			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000316	PMID:21596366	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0008897	PMID:21596366	PCS		7/7			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0001500	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0008734	PMID:21596366	PCS		4/4			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0002216	PMID:21596366	PCS		6/9			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000278	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0005922	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0009803	OMIM:300845	TAS					P	HPO:skoehler[2012-10-16]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0001644	PMID:21596366	PCS		3/7			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0001342	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0005288	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000490	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0011969	PMID:21596366	PCS		7/7			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0001263	OMIM:300845	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0034323	PMID:21596366	PCS		4/9			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0005181	PMID:21596366	PCS		1/9			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0001419	PMID:21596366	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0012020	PMID:21596366	PCS		1/2			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000508	PMID:21596366	PCS		6/9			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000822	PMID:21596366	PCS		3/9			P	HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000824	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0200055	OMIM:300845	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0001711	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000369	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0002401	PMID:21596366	PCS		5/7			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000027	PMID:21596366	PCS		3/3			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-05-13]
OMIM:300845	Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism,and facial dysmorphism		HP:0000445	OMIM:300845	TAS					P	HPO:skoehler[2012-10-14]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0003577	PMID:26880018	PCS		1/1			C	HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0007814	PMID:26880018	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0001156	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000540	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0004322	OMIM:617102	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0010049	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0001270	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0010306	PMID:26880018	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0010743	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000639	PMID:26880018	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0010230	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0012471	PMID:26880018	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0009882	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000774	PMID:26880018	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0009803	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000670	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0009826	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000431	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0002079	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000293	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0002098	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0011800	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0005280	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0003180	OMIM:617102	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0100259	PMID:26880018	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000506	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0032078	PMID:26880018	PCS		1/1			P	HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000007	PMID:26880018	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000348	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0001538	PMID:26880018	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000268	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0001852	OMIM:617102	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000369	PMID:26880018	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:617102	Short-Rib thoracic dysplasia 16 with or without polydactyly		HP:0000687	PMID:26880018	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-04]
OMIM:618231	Epidermodysplasia verruciformis 2		HP:0006739	PMID:28646613	PCS		1/4			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618231	Epidermodysplasia verruciformis 2		HP:0000007	PMID:28646613	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618231	Epidermodysplasia verruciformis 2		HP:0020114	PMID:28646613	PCS					P	HPO:probinson[2020-07-23]
OMIM:618231	Epidermodysplasia verruciformis 2		HP:0550004	PMID:28646613	PCS	HP:0011463	4/4			P	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:608022	Diaphanospondylodysostosis		HP:0000286	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0005257	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0003275	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0001252	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0003196	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000085	PMID:30006055	PCS		1/3			P	HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0001290	OMIM:608022	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608022	Diaphanospondylodysostosis		HP:0001804	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000316	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000239	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0002779	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0001765	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0003521	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0006615	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000175	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0004331	PMID:30006055	PCS		3/3			P	HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0001263	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0034199	PMID:30006055	PCS		2/3			C	HPO:probinson[2022-12-10];HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0010880	PMID:30006055	PCS		2/3			P	HPO:probinson[2015-02-21];HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0034198	PMID:30006055	PCS		1/3			C	HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0000800	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000921	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000007	PMID:20869035	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0008643	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0001538	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000369	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0002089	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000023	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0001591	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0031096	PMID:30006055	PCS		3/3			P	HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0008435	PMID:30006055	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0000457	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0001562	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0003422	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0001762	PMID:30006055	PCS		1/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0002098	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000470	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0002093	OMIM:608022	TAS					P	HPO:skoehler[2010-06-20]
OMIM:608022	Diaphanospondylodysostosis		HP:0005280	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0100880	OMIM:608022	TAS					P	HPO:skoehler[2014-01-28]
OMIM:608022	Diaphanospondylodysostosis		HP:0100752	OMIM:608022	TAS					P	HPO:probinson[2015-02-21]
OMIM:608022	Diaphanospondylodysostosis		HP:0200133	OMIM:608022	TAS					P	HPO:skoehler[2013-06-11]
OMIM:608022	Diaphanospondylodysostosis		HP:0001511	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0025706	PMID:30006055	PCS		1/3			P	HPO:probinson[2022-12-10]
OMIM:608022	Diaphanospondylodysostosis		HP:0000465	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000105	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0000347	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0002126	OMIM:608022	TAS					P	HPO:probinson[2009-02-17]
OMIM:608022	Diaphanospondylodysostosis		HP:0030290	OMIM:608022	TAS					P	HPO:skoehler[2015-04-05]
OMIM:613364	Spastic paraplegia 41, autosomal dominant		HP:0000012	OMIM:613364	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613364	Spastic paraplegia 41, autosomal dominant		HP:0007340	OMIM:613364	TAS				HP:0012840	P	HPO:skoehler[2013-06-06]
OMIM:613364	Spastic paraplegia 41, autosomal dominant		HP:0002064	OMIM:613364	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613364	Spastic paraplegia 41, autosomal dominant		HP:0001258	OMIM:613364	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613364	Spastic paraplegia 41, autosomal dominant		HP:0000006	OMIM:613364	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613364	Spastic paraplegia 41, autosomal dominant		HP:0001347	OMIM:613364	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615715	Bone marrow failure syndrome 2		HP:0000252	PMID:24507776	PCS		2/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0003621	PMID:24507776	PCS		2/3			C	HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0000992	PMID:24507776	PCS		0/3			P	HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0025708	PMID:24507776	PCS		1/3			C	HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0001882	PMID:24507776	PCS		3/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0001903	PMID:24507776	PCS		3/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0000007	PMID:24507776	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0001319	PMID:24507776	PCS		1/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0005528	PMID:24507776	PCS		3/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-06-05]
OMIM:615715	Bone marrow failure syndrome 2		HP:0001873	PMID:24507776	PCS		3/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2023-06-05]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0003477	PMID:35986737	PCS		11/21			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0002015	PMID:35986737	PCS		9/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0003621	PMID:35986737	PCS					C	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0002395	PMID:35986737	PCS		24/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0002066	PMID:35986737	PCS		28/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0001260	PMID:35986737	PCS		9/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0002495	PMID:35986737	PCS		24/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0003581	PMID:35986737	PCS					C	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0001152	PMID:35986737	PCS		16/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0002061	PMID:35986737	PCS		24/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0010871	PMID:35986737	PCS		2/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0002080	PMID:35986737	PCS		18/31			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0011463	PMID:35986737	PCS					C	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0000648	PMID:35986737	PCS		9/17			P	HPO:probinson[2023-06-11]
OMIM:620221	Spastic paraplegia 79A, autosomal dominant		HP:0000006	PMID:35986737	PCS					I	HPO:probinson[2023-04-16]
OMIM:177650	Exfoliation syndrome		HP:0001132	OMIM:177650	TAS					P	HPO:skoehler[2013-07-17]
OMIM:177650	Exfoliation syndrome		HP:0009916	OMIM:177650	TAS					P	HPO:skoehler[2014-01-28]
OMIM:177650	Exfoliation syndrome		HP:0012629	OMIM:177650	TAS					P	HPO:skoehler[2014-01-28]
OMIM:177650	Exfoliation syndrome		HP:0002063	OMIM:177650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:177650	Exfoliation syndrome		HP:0012635	OMIM:177650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:177650	Exfoliation syndrome		HP:0012636	OMIM:177650	TAS					P	HPO:skoehler[2014-01-28]
OMIM:177650	Exfoliation syndrome		HP:0011499	OMIM:177650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:177650	Exfoliation syndrome		HP:0012627	OMIM:177650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:177650	Exfoliation syndrome		HP:0012631	OMIM:177650	TAS					P	HPO:skoehler[2014-01-28]
OMIM:177650	Exfoliation syndrome		HP:0012633	OMIM:177650	TAS					P	HPO:skoehler[2014-01-28]
OMIM:177650	Exfoliation syndrome		HP:0000518	OMIM:177650	IEA					P	HPO:skoehler[2018-10-08]
OMIM:177650	Exfoliation syndrome		HP:0000517	OMIM:177650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:177650	Exfoliation syndrome		HP:0000006	OMIM:177650	IEA					I	HPO:iea[2009-02-17]
OMIM:177650	Exfoliation syndrome		HP:0000501	OMIM:177650	IEA					P	HPO:skoehler[2010-06-20]
OMIM:184900	Stiff skin syndrome		HP:0003577	PMID:20375004	PCS		8/8			C	HPO:probinson[2024-03-22]
OMIM:184900	Stiff skin syndrome		HP:0004322	PMID:20375004	PCS		HP:0040283			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0002020	PMID:20375004	PCS		4/8			P	HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0012385	PMID:20375004	PCS		8/8			P	HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0006380	PMID:20375004	PCS		7/8			P	HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0000518	PMID:20375004	PCS	HP:0003596	2/8			P	HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0009830	PMID:20375004	PCS		2/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0001647	PMID:20375004	PCS		1/8			P	HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0009125	PMID:20375004	PCS		HP:0040283			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0030053	PMID:20375004	PCS		8/8			P	HPO:skoehler[2015-01-27];HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0001324	PMID:20375004	PCS		HP:0040283			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0006467	PMID:20375004	PCS		7/8			P	HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0002987	PMID:20375004	PCS		8/8			P	HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0000006	PMID:20375004	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-26]
OMIM:184900	Stiff skin syndrome		HP:0000545	PMID:20375004	PCS		6/8			P	HPO:probinson[2021-05-26]
OMIM:620547	Spermatogenic failure 88		HP:0003251	PMID:35587281;PMID:29790874	PCS		3/3			P	HPO:probinson[2024-03-08]
OMIM:620547	Spermatogenic failure 88		HP:0011462	PMID:29790874	PCS		2/2			C	HPO:probinson[2024-03-08]
OMIM:620547	Spermatogenic failure 88		HP:0000007	PMID:29790874	PCS					I	HPO:probinson[2024-03-08]
OMIM:620547	Spermatogenic failure 88		HP:0011961	PMID:35587281;PMID:29790874	PCS		3/3			P	HPO:probinson[2024-03-08]
OMIM:620547	Spermatogenic failure 88		HP:0031039	PMID:29790874	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0003676	PMID:25063546	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0006824	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002980	PMID:25063546	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002385	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0003155	PMID:25063546	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0003991	PMID:25063546	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0003097	PMID:25063546	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0003072	PMID:25063546	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0004618	PMID:25063546	PCS	HP:0011463	1/1			P	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002659	PMID:25063546	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002953	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002315	PMID:25063546	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0008513	PMID:25063546	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002797	OMIM:602080	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002512	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002653	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002694	PMID:25063546	PCS	HP:0011463	1/1			P	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002273	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0003084	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0003080	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0034197	PMID:25063546	PCS		1/1			C	HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0006480	PMID:25063546	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-03]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0006487	OMIM:602080	IEA					P	HPO:skoehler[2019-09-07]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0002423	OMIM:602080	IEA					P	HPO:iea[2009-02-17]
OMIM:602080	Paget disease of bone 2, early-onset		HP:0000006	PMID:10615125	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0000939	OMIM:612287	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0000938	OMIM:612287	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0000117	OMIM:612287	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0003109	OMIM:612287	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0002659	OMIM:612287	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0000006	OMIM:612287	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0000787	OMIM:612287	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612287	Nephrolithiasis/osteoporosis, hypophosphatemic, 2		HP:0002148	OMIM:612287	IEA					P	HPO:skoehler[2010-06-19]
OMIM:301018	Deafness, X-linked 7		HP:0003577	PMID:28096187	PCS		6/6			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000365	PMID:28096187	PCS		6/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000574	PMID:28096187	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000431	PMID:28096187	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0001263	PMID:28096187	PCS		0/4			P	HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0011480	PMID:28096187	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000506	PMID:28096187	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0001419	PMID:28096187	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000508	PMID:28096187	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000413	PMID:28096187	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0001249	PMID:28096187	PCS		0/4			P	HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000358	PMID:28096187	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:301018	Deafness, X-linked 7		HP:0000402	PMID:28096187	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:212070	Carboxypeptidase N deficiency		HP:6000560	PMID:12560874	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:212070	Carboxypeptidase N deficiency		HP:0001025	PMID:12560874	PCS					P	HPO:probinson[2023-03-05]
OMIM:212070	Carboxypeptidase N deficiency		HP:0100665	PMID:12560874	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:212070	Carboxypeptidase N deficiency		HP:0000007	PMID:12560874	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:212070	Carboxypeptidase N deficiency		HP:0003193	PMID:12560874	PCS					P	HPO:probinson[2023-03-05]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0003621	PMID:34957489	PCS		3/6			C	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0003236	PMID:34957489	PCS		6/6			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0003687	PMID:34957489	PCS		1/5			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0003201	PMID:34957489	PCS		6/6		HP:0031796	P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0000083	PMID:34957489	PCS		2/6			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0002460	PMID:34957489	PCS		1/6			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0010602	PMID:34957489	PCS		1/5			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0011462	PMID:34957489	PCS		3/6			C	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0000007	PMID:34957489	PCS					I	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0012071	PMID:34957489	PCS		0/6			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0003557	PMID:34957489	PCS		3/5			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0003546	PMID:34957489	PCS		3/6			P	HPO:probinson[2023-06-17]
OMIM:620235	Rhabdomyolysis, susceptibility to, 1		HP:0003326	PMID:34957489	PCS		5/6			P	HPO:probinson[2023-06-17]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0000365	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0000034	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0002079	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0002151	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0002273	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0010841	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0001290	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0011923	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0100660	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0012469	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0009141	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0000007	PMID:29211846	PCS					I	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0001935	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0001257	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0000047	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0007359	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:618972	Mitochondrial DNA depletion syndrome 19		HP:0001336	PMID:29211846	PCS		1/1			P	HPO:probinson[2020-09-13]
OMIM:613827	Retinitis pigmentosa 48		HP:0000608	PMID:15452722	PCS					P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:613827	Retinitis pigmentosa 48		HP:0000505	PMID:15452722	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-21]
OMIM:613827	Retinitis pigmentosa 48		HP:0000510	PMID:15452722	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-21]
OMIM:613827	Retinitis pigmentosa 48		HP:0000006	PMID:15452722	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-21]
OMIM:614190	Pigmented nodular adrenocortical disease, primary, 3		HP:0008221	OMIM:614190	TAS					P	HPO:probinson[2013-08-10]
OMIM:614190	Pigmented nodular adrenocortical disease, primary, 3		HP:0003118	OMIM:614190	TAS					P	HPO:probinson[2013-08-10]
OMIM:614190	Pigmented nodular adrenocortical disease, primary, 3		HP:0000006	OMIM:614190	TAS					I	HPO:probinson[2013-08-10]
OMIM:618782	Long QT syndrome 16		HP:0003577	PMID:25460178	PCS		1/1			C	HPO:probinson[2022-07-04]
OMIM:618782	Long QT syndrome 16		HP:0012266	PMID:25460178	PCS	HP:0003577	1/1			P	HPO:probinson[2020-05-10]
OMIM:618782	Long QT syndrome 16		HP:0001662	PMID:25460178	PCS	HP:0003577	1/1			P	HPO:probinson[2020-05-10]
OMIM:618782	Long QT syndrome 16		HP:0011706	PMID:25460178	PCS	HP:0003577	1/1			P	HPO:probinson[2020-05-10]
OMIM:618782	Long QT syndrome 16		HP:0011682	PMID:25460178	PCS	HP:0003577	1/1			P	HPO:probinson[2020-05-10]
OMIM:618782	Long QT syndrome 16		HP:0005184	PMID:25460178	PCS	HP:0003577	1/1			P	HPO:probinson[2020-05-10]
OMIM:618782	Long QT syndrome 16		HP:0011648	PMID:25460178	PCS	HP:0003577	1/1			P	HPO:probinson[2020-05-10]
OMIM:618782	Long QT syndrome 16		HP:0000006	PMID:25460178	PCS					I	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:300448	Alpha-Thalassemia myelodysplasia syndrome		HP:0011907	PMID:12858175	PCS					P	HPO:probinson[2013-02-17]
OMIM:300448	Alpha-Thalassemia myelodysplasia syndrome		HP:0004840	PMID:15358626	PCS					P	HPO:probinson[2013-02-17]
OMIM:300448	Alpha-Thalassemia myelodysplasia syndrome		HP:0011903	PMID:15358626	PCS					P	HPO:probinson[2013-02-18]
OMIM:300448	Alpha-Thalassemia myelodysplasia syndrome		HP:0002863	PMID:12858175	PCS					P	HPO:probinson[2013-01-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0002421	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001332	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001250	OMIM:616977	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000160	PMID:26153216	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001252	PMID:26153216	PCS		3/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0003593	PMID:26153216	PCS		1/3			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0002020	OMIM:616977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001251	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0033128	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0033725	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000718	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000316	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0025336	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000752	PMID:26153216	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001642	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001763	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001249	PMID:26153216	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001007	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000252	PMID:26153216	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001385	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001344	OMIM:616977	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0002079	PMID:26153216	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0011968	OMIM:616977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001263	PMID:26153216	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001182	PMID:26153216	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0011094	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000729	OMIM:616977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001537	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0002307	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000322	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000006	PMID:23020937	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000582	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0003577	PMID:26153216	PCS		2/3			C	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000540	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000463	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0001508	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0008551	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0012450	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000739	OMIM:616977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000219	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0009765	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000218	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000212	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000431	PMID:26153216	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0006913	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000750	PMID:26153216	PCS		2/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0031936	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0009907	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0100710	PMID:26153216	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000426	OMIM:616977	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000348	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:616977	Intellectual developmental disorder, autosomal dominant 43		HP:0000664	PMID:26153216	PCS		1/3			P	HPO:probinson[2022-06-09]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0004940	PMID:15940697	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0003577	PMID:15940697	PCS		2/2			C	HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0004322	OMIM:208000	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001640	PMID:15940697	PCS		2/2			P	HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0025477	PMID:11159191	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0031013	OMIM:208000	IEA					P	HPO:skoehler[2019-02-22]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0031313	PMID:15940697	PCS		2/2			P	HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0031314	PMID:15940697	PCS		2/2			P	HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0100545	PMID:15940697	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001717	OMIM:208000	IEA					P	HPO:iea[2009-02-17]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001507	OMIM:208000	IEA					P	HPO:iea[2009-02-17]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001658	OMIM:208000	IEA					P	HPO:iea[2009-02-17]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0000822	PMID:15940697	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001635	PMID:11159191	PCS	HP:0003623	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001635	PMID:15940697	PCS		1/2			P	HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0000007	PMID:11159191	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0025116	PMID:11159191	PCS		1/1			P	HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0004912	OMIM:208000	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001920	PMID:11159191	PCS	HP:0003593	1/1			P	HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0002643	PMID:15940697	PCS		1/2			P	HPO:probinson[2022-08-11];HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0003623	PMID:11159191	PCS		1/1			C	HPO:probinson[2022-08-11]
OMIM:208000	Arterial calcification, generalized, of infancy, 1		HP:0001644	PMID:11159191	PCS	HP:0003623	1/1			P	HPO:probinson[2022-08-11]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000044	PMID:31006512	PCS		5/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000582	PMID:31006512	PCS		2/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0003577	PMID:31006512	PCS		9/9			C	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0004322	PMID:31006512	PCS		8/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001250	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001272	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0003298	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001252	PMID:31006512	PCS		4/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0003196	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0012745	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0010882	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0100962	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0002719	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001629	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000817	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0008551	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000733	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0002714	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000411	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000278	PMID:31006512	PCS		2/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001249	PMID:31006512	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0004415	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0008757	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000154	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0002575	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0002059	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000252	PMID:31006512	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0002650	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000276	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0011968	PMID:31006512	PCS		2/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0002032	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000193	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001263	PMID:31006512	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0005280	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0100710	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001419	PMID:31006512	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000729	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0005819	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0004209	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001511	PMID:31006512	PCS		2/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000565	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001631	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001510	PMID:31006512	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0001257	PMID:31006512	PCS		1/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0007018	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000586	PMID:31006512	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:301030	Van Esch-O'Driscoll syndrome		HP:0000960	PMID:31006512	PCS		2/9			P	HPO:probinson[2022-08-28]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0000708	PMID:17236128	PCS		1/8			P	HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0002783	PMID:17236128	PCS		1/8			P	HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0001250	PMID:17236128	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0001263	PMID:17236128	PCS		1/8			P	HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0003593	PMID:17236128	PCS		1/1			C	HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0001019	PMID:17236128	PCS		1/8			P	HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0001249	PMID:17236128	PCS		2/8			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0000006	PMID:17236128	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-27]
OMIM:136630	Intellectual developmental disorder, autosomal dominant, FRA12A type		HP:0000962	PMID:17236128	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-27]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0000486	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0000343	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001252	PMID:30335141	PCS		2/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0003593	PMID:30335141	PCS		5/5			C	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001290	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0000219	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0025336	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0003701	PMID:30335141	PCS		2/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001324	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001763	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001348	PMID:30335141	PCS		2/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0002058	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0000494	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0002136	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0000750	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0000276	PMID:30335141	PCS		2/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001288	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0031936	PMID:30335141	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0003487	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0000490	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001263	PMID:30335141	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0011800	PMID:30335141	PCS		1/5			P	HPO:skoehler[2019-04-18]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0009890	PMID:30335141	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0001419	PMID:30335141	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0025502	PMID:30335141	PCS		2/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0002307	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0004209	PMID:30335141	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:301024	Intellectual developmental disorder, X-linked 108		HP:0007018	PMID:30335141	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:176200	Porphyria variegata		HP:0000992	OMIM:176200	TAS					P	HPO:probinson[2009-02-17]
OMIM:176200	Porphyria variegata		HP:0002013	OMIM:176200	TAS					P	HPO:probinson[2009-02-17]
OMIM:176200	Porphyria variegata		HP:0003163	PMID:8852667;PMID:29516370	PCS		5/5			P	HPO:probinson[2022-05-29]
OMIM:176200	Porphyria variegata		HP:0012217	PMID:8852667;PMID:29516370	PCS		5/5			P	HPO:probinson[2022-05-29]
OMIM:176200	Porphyria variegata		HP:0003470	OMIM:176200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:176200	Porphyria variegata		HP:0000709	OMIM:176200	TAS					P	HPO:probinson[2009-02-17]
OMIM:176200	Porphyria variegata		HP:0034283	PMID:8852667	PCS		4/4			P	HPO:probinson[2022-06-04]
OMIM:176200	Porphyria variegata		HP:0010473	OMIM:176200;PMID:29516370	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:176200	Porphyria variegata		HP:0011462	PMID:29516370	PCS		1/1			C	HPO:probinson[2022-05-29]
OMIM:176200	Porphyria variegata		HP:0009830	OMIM:176200	TAS					P	HPO:probinson[2009-02-17]
OMIM:176200	Porphyria variegata		HP:0001649	OMIM:176200	TAS					P	HPO:probinson[2009-02-17]
OMIM:176200	Porphyria variegata		HP:0002019	OMIM:176200	TAS					P	HPO:probinson[2009-02-17]
OMIM:176200	Porphyria variegata		HP:0000006	OMIM:176200	TAS					I	HPO:probinson[2009-02-17]
OMIM:176200	Porphyria variegata		HP:0002027	PMID:29516370	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0003037	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0003510	OMIM:313420	IEA					P	HPO:skoehler[2010-06-20]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000486	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0001597	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000463	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0002167	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0003273	OMIM:313420	TAS					P	HPO:probinson[2013-04-01]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000280	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0009381	OMIM:313420	IEA					P	HPO:skoehler[2018-10-08]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000639	OMIM:313420	IEA					P	HPO:skoehler[2010-06-20]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0011342	OMIM:313420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000316	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0002878	OMIM:313420	TAS					P	HPO:skoehler[2014-06-24]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0001423	OMIM:313420	TAS					I	HPO:skoehler[2017-07-13]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0002657	OMIM:313420	TAS					P	HPO:skoehler[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0001187	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000431	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0002694	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0001182	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0002093	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0005280	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0006380	OMIM:313420	TAS					P	HPO:skoehler[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0002808	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000926	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0002944	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0000768	OMIM:313420	IEA					P	HPO:iea[2009-02-17]
OMIM:313420	Spondylometaphyseal dysplasia, X-linked		HP:0001417	OMIM:313420	IEA					I	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0002476	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0010529	OMIM:172700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:172700	Pick disease of brain		HP:0002463	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0002145	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0030213	OMIM:172700	TAS					P	HPO:skoehler[2015-01-04]
OMIM:172700	Pick disease of brain		HP:0030223	OMIM:172700	TAS					P	HPO:skoehler[2015-01-04]
OMIM:172700	Pick disease of brain		HP:0002591	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0002171	OMIM:172700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:172700	Pick disease of brain		HP:0000737	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000748	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000734	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000745	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000733	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0002529	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000741	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0003745	OMIM:172700	IEA					I	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000751	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000006	OMIM:172700	IEA					I	HPO:iea[2009-02-17]
OMIM:172700	Pick disease of brain		HP:0000710	OMIM:172700	IEA					P	HPO:iea[2009-02-17]
OMIM:616963	Hypercalcemia, infantile 2		HP:0000121	PMID:26047794	PCS		15/15			P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0012408	PMID:26047794	PCS					P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0001508	PMID:26047794	PCS		11/15			P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0001252	PMID:26047794	PCS		4/15			P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0000007	PMID:26047794	PCS					I	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0002150	PMID:26047794	PCS		12/15			P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0000117	PMID:26047794	PCS					P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0003072	PMID:26047794	PCS					P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0000103	PMID:26047794	PCS		11/14			P	HPO:probinson[2017-06-23]
OMIM:616963	Hypercalcemia, infantile 2		HP:0002148	PMID:26047794	PCS					P	HPO:probinson[2017-06-23]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0003015	OMIM:215045	TAS				HP:0012828	P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0001561	OMIM:215045	TAS					P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0002983	OMIM:215045	TAS					P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0004233	OMIM:215045	TAS					P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0030674	PMID:9268097	PCS		2/2			C	HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0003177	OMIM:215045	TAS					P	HPO:probinson[2012-07-30]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0001791	PMID:9268097	PCS		2/2			P	HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0000272	OMIM:215045	TAS				HP:0012828	P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0005151	PMID:9268097	PCS		2/2			P	HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0005280	PMID:9268097	PCS		2/2			P	HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0003826	PMID:9649554	PCS		1/1			C	HPO:probinson[2009-02-17];HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0001789	PMID:9268097	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0000007	PMID:9649554	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0008754	OMIM:215045	TAS					P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0000774	PMID:9268097	PCS		2/2			P	HPO:probinson[2023-03-01]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0005616	OMIM:215045	TAS					P	HPO:probinson[2012-07-30]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0000773	PMID:9268097	PCS		2/2			P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0000347	PMID:9268097	PCS		2/2			P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0003468	PMID:10664159	PCS		0/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-08]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0001622	OMIM:215045	TAS					P	HPO:probinson[2009-02-17]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0005789	OMIM:215045	TAS	HP:0003577				P	HPO:probinson[2012-07-30]
OMIM:215045	Chondrodysplasia, Blomstrand type		HP:0008108	OMIM:215045	TAS					P	HPO:probinson[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001650	OMIM:253010	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0007759	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0007957	PMID:33558080	PCS		3/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003277	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000365	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000683	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003311	OMIM:253010;PMID:33558080	PCS		14/19			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001251	PMID:33558080	PCS		2/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000280	PMID:33558080	PCS		6/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0005292	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0033725	PMID:33558080	PCS		2/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0012070	PMID:33558080	PCS		4/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003307	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003308	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002857	OMIM:253010	IEA		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001249	PMID:33558080	PCS		0/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003521	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003049	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001385	PMID:33558080	PCS		2/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001223	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002673	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001387	PMID:33558080	PCS		1/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001382	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0012069	OMIM:253010	TAS					P	HPO:probinson[2012-08-04]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0008166	PMID:33558080	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000926	PMID:33558080	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000007	PMID:33558080	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000884	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002788	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001653	PMID:33558080	PCS		5/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000687	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0001776	PMID:33558080	PCS		2/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003016	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000023	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003053	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002240	PMID:33558080	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003090	PMID:33558080	PCS		4/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000939	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002318	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000154	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000670	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003621	OMIM:253010	IEA					C	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002650	PMID:33558080	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0003300	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002091	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0002808	PMID:33558080	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000904	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000943	PMID:33558080	PCS		6/9			P	HPO:probinson[2023-01-25]
OMIM:253010	Mucopolysaccharidosis type IVB (Morquio)		HP:0000303	OMIM:253010	IEA					P	HPO:iea[2009-02-17]
OMIM:619488	DEGCAGS syndrome		HP:0001177	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000365	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000089	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002780	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002021	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0003196	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002020	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0010442	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0012622	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000639	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0012471	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000998	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001605	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002779	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000512	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000358	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001601	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002036	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000252	PMID:33875846	PCS		6/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000010	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0005301	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002033	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0012584	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000407	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0012582	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000007	PMID:33875846	PCS					I	HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000527	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000400	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000520	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0025408	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000369	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001396	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000343	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0005599	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0005235	PMID:33875846	PCS		4/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000463	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000980	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000062	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001274	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002240	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0010943	PMID:33875846	PCS	HP:0011461	1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0012447	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002119	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000218	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001945	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0004810	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001561	PMID:33875846	PCS	HP:0011461	1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002376	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002099	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002092	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002090	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0100957	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0040288	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000508	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0200136	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001159	PMID:33875846	PCS		4/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001433	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000347	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001770	PMID:33875846	PCS		3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001891	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0010808	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001252	PMID:33875846	PCS		6/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001010	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000041	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000280	PMID:33875846	PCS		3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000319	PMID:33875846	PCS		3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0011100	PMID:33875846	PCS		4/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000316	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001528	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001649	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002857	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002216	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001643	PMID:33875846	PCS	HP:0003623	1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001642	PMID:33875846	PCS		3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000278	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001249	PMID:33875846	PCS		6/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002750	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0011968	PMID:33875846	PCS		3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001263	PMID:33875846	PCS		6/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000294	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002904	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0012384	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000448	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000601	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000568	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0009778	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000047	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000960	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000325	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001655	PMID:33875846	PCS	HP:0003623	1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0006528	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001195	PMID:33875846	PCS	HP:0003577	2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002162	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002719	PMID:33875846	PCS		3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001508	PMID:33875846	PCS		6/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001629	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001903	PMID:33875846	PCS		4/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000938	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0100507	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000499	PMID:33875846	PCS		4/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000534	PMID:33875846	PCS		3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001623	PMID:33875846	PCS	HP:0003577	1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0040119	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001622	PMID:33875846	PCS	HP:0003577	4/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000154	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001000	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001363	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0030842	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001762	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001882	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0005164	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0011035	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0009110	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001518	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001999	PMID:33875846	PCS		11/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000426	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001511	PMID:33875846	PCS	HP:0011461	3/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000664	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001357	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001631	PMID:33875846	PCS	HP:0003577	2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0001876	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0000028	PMID:33875846	PCS		3/13	MALE		P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0025429	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0200053	PMID:33875846	PCS		1/13			P	HPO:probinson[2021-10-04]
OMIM:619488	DEGCAGS syndrome		HP:0002721	PMID:33875846	PCS		2/13			P	HPO:probinson[2021-10-04]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0003621	PMID:33956074	PCS		4/5			C	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0001541	PMID:33956074	PCS		2/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0002240	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0031364	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0002040	PMID:33956074	PCS		7/9			P	HPO:probinson[2021-11-01];HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0011954	PMID:33956074	PCS		2/5			P	HPO:probinson[2021-11-01];HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0030948	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0012378	PMID:33956074	PCS		2/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0002719	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0001409	PMID:33956074	PCS					P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0011463	PMID:33956074	PCS		1/5			C	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0000007	PMID:33956074	PCS					I	HPO:probinson[2021-10-22];HPO:probinson[2021-10-22]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0000967	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01];HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0001873	PMID:33956074	PCS		8/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0000421	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0002910	PMID:33956074	PCS					P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0001744	PMID:33956074	PCS		9/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0001402	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01]
OMIM:619463	Portal hypertension, noncirrhotic, 2		HP:0002105	PMID:33956074	PCS		1/9			P	HPO:probinson[2021-11-01]
OMIM:147750	IVIC syndrome		HP:0000143	PMID:17256792	PCS		1/26			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0001199	PMID:17256792	PCS		5/26			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0003577	PMID:17256792	PCS					C	HPO:probinson[2022-03-23]
OMIM:147750	IVIC syndrome		HP:0002023	PMID:17256792	PCS		3/26			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0001498	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0000365	PMID:17256792	PCS		22/24			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0000486	PMID:17256792	PCS		2/26			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0003097	PMID:17256792	PCS	HP:0011463	8/8			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0010034	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0030241	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0009702	PMID:17256792	PCS		8/19			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0001643	PMID:17256792	PCS		1/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0008953	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0000894	PMID:17256792	PCS		4/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0002996	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0002974	OMIM:147750	TAS					P	HPO:probinson[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0009824	PMID:17256792	PCS		10/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0002650	PMID:17256792	PCS		9/19			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0001245	PMID:17256792	PCS		4/19			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0003022	PMID:17256792	PCS		4/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0100258	PMID:17256792	PCS		6/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0006064	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0033980	PMID:33783914	PCS		3/4			P	HPO:probinson[2021-07-16]
OMIM:147750	IVIC syndrome		HP:0001636	PMID:17256792	PCS		1/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0009777	PMID:17256792	PCS		8/26			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0002007	PMID:17256792	PCS		5/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0006248	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0001873	PMID:17256792	PCS		13/21			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0009778	PMID:17256792	PCS		8/26			P	HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0000006	PMID:17256792	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-09]
OMIM:147750	IVIC syndrome		HP:0002984	OMIM:147750	TAS					P	HPO:probinson[2012-06-03]
OMIM:147750	IVIC syndrome		HP:0002566	OMIM:147750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147750	IVIC syndrome		HP:0000544	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:147750	IVIC syndrome		HP:0001974	OMIM:147750	IEA					P	HPO:iea[2009-02-17]
OMIM:600132	Retinitis pigmentosa 14		HP:0000550	PMID:17620573	PCS		5/5			P	HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0001133	PMID:17620573	PCS					P	HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0007737	PMID:17620573	IEA					P	HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0000662	PMID:17620573	PCS	HP:0003593	5/5			P	HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0000639	PMID:17620573	PCS	HP:0003593	5/5			P	HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0008043	PMID:17620573	TAS					P	HP:probinson[2019-01-20];HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0000007	PMID:17620573	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0007663	PMID:17620573	PCS	HP:0003593	5/5			P	HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0000510	PMID:17620573	PCS		5/5			P	HPO:iea[2009-02-17];HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0007787	PMID:17620573	PCS		5/5			P	HP:probinson[2019-01-20]
OMIM:600132	Retinitis pigmentosa 14		HP:0000543	PMID:17620573	PCS					P	HP:probinson[2019-01-20]
OMIM:613628	Odontoid hypoplasia		HP:0003467	OMIM:613628	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613628	Odontoid hypoplasia		HP:0003311	OMIM:613628	TAS					P	HPO:skoehler[2015-01-21]
OMIM:613628	Odontoid hypoplasia		HP:0008462	OMIM:613628	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613628	Odontoid hypoplasia		HP:0040143	OMIM:613628	TAS					P	HPO:skoehler[2015-01-28]
OMIM:613628	Odontoid hypoplasia		HP:0000006	OMIM:613628	TAS					I	HPO:skoehler[2012-10-17]
OMIM:113301	Brachydactyly, type e, with atrial septal defect, type II		HP:0005863	OMIM:113301	TAS					P	HPO:probinson[2012-07-16]
OMIM:113301	Brachydactyly, type e, with atrial septal defect, type II		HP:0004322	OMIM:113301	IEA					P	HPO:iea[2009-02-17]
OMIM:113301	Brachydactyly, type e, with atrial septal defect, type II		HP:0010044	OMIM:113301	IEA					P	HPO:iea[2009-02-17]
OMIM:113301	Brachydactyly, type e, with atrial septal defect, type II		HP:0000311	OMIM:113301	IEA					P	HPO:iea[2009-02-17]
OMIM:113301	Brachydactyly, type e, with atrial septal defect, type II		HP:0001631	OMIM:113301	IEA					P	HPO:iea[2009-02-17]
OMIM:113301	Brachydactyly, type e, with atrial septal defect, type II		HP:0000006	OMIM:113301	IEA					I	HPO:iea[2009-02-17]
OMIM:113301	Brachydactyly, type e, with atrial septal defect, type II		HP:0010743	OMIM:113301	IEA					P	HPO:iea[2009-02-17]
OMIM:303800	Colorblindness, deutan		HP:0003577	PMID:12626747	PCS					C	HPO:probinson[2022-05-04]
OMIM:303800	Colorblindness, deutan		HP:0001419	PMID:10319869	PCS					I	HPO:probinson[2012-04-06];HPO:probinson[2022-05-04]
OMIM:303800	Colorblindness, deutan		HP:0011520	PMID:10319869	PCS					P	HPO:probinson[2012-04-06];HPO:probinson[2022-05-04]
OMIM:614621	UV-sensitive syndrome 2		HP:0003224	PMID:19329487	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:614621	UV-sensitive syndrome 2		HP:0000992	PMID:19329487	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:614621	UV-sensitive syndrome 2		HP:0001480	PMID:19329487	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:614621	UV-sensitive syndrome 2		HP:0010472	PMID:19329487	PCS		0/1			P	HPO:probinson[2022-04-10]
OMIM:614621	UV-sensitive syndrome 2		HP:0003593	PMID:19329487	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:614621	UV-sensitive syndrome 2		HP:0000007	PMID:19329487	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:604432	Spinocerebellar ataxia 11		HP:0003621	PMID:18037885	PCS		7/20			C	HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0002078	PMID:18037885	PCS		18/18			P	HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0001272	PMID:18037885	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0001260	PMID:18037885	PCS		21/21			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0002066	PMID:18037885	PCS		21/21			P	HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0003584	PMID:18037885	PCS		1/20			C	HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0002141	PMID:18037885	PCS					P	HPO:probinson[2023-04-02];HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0002073	PMID:18037885	PCS		21/21			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0002070	PMID:18037885	PCS		20/21			P	HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0000639	PMID:18037885	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0011462	PMID:18037885	PCS		12/20			C	HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0008003	PMID:18037885	PCS		18/18			P	HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0000006	PMID:18037885	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:604432	Spinocerebellar ataxia 11		HP:0001347	PMID:18037885	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:108721	Atelosteogenesis, type III		HP:0002982	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0001234	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0008905	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0004976	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0004632	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0000175	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0002650	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0001762	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0003440	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0003042	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0000272	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0000470	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0011800	OMIM:108721	TAS					P	HPO:skoehler[2013-11-28]
OMIM:108721	Atelosteogenesis, type III		HP:0005280	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0003180	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0006060	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0000327	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0002947	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0006200	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0002007	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0002986	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0001852	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0000006	PMID:14991055	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-04]
OMIM:108721	Atelosteogenesis, type III		HP:0000347	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:108721	Atelosteogenesis, type III		HP:0000269	OMIM:108721	IEA					P	HPO:iea[2009-02-17]
OMIM:151640	Lip, hamartomatous		HP:0000153	OMIM:151640	IEA					P	HPO:iea[2009-02-17]
OMIM:151640	Lip, hamartomatous		HP:0010566	OMIM:151640	IEA					P	HPO:skoehler[2010-06-20]
OMIM:151640	Lip, hamartomatous		HP:0000006	OMIM:151640	IEA					I	HPO:iea[2009-02-17]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0033606	PMID:25129144	PCS		13/14			P	HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0004322	PMID:25129144	PCS		2/14			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0001508	PMID:25129144	PCS		1/14			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0002718	PMID:25129144	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0003593	PMID:25129144	PCS					C	HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0000007	PMID:25129144	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0000403	PMID:25129144	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0002205	PMID:25129144	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2022-10-06]
OMIM:616022	Neutropenia, severe congenital, 6, autosomal recessive		HP:0001875	PMID:25129144	PCS		12/12			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-10-06]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000286	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0003577	PMID:30500825	PCS					C	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0001344	PMID:30500825	PCS		7/11			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000750	PMID:30500825	PCS		11/11			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000431	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0031936	PMID:30500825	PCS		8/11			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000463	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0001250	PMID:30500825	PCS		6/11			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0002263	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0001252	PMID:30500825	PCS		10/11			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0001263	PMID:30500825	PCS		11/11			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0004691	PMID:30500825	PCS		2/6			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0011228	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000729	PMID:30500825	PCS		3/3			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0011220	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000508	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000219	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000307	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0030084	PMID:30500825	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000322	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000006	PMID:30500825	PCS					I	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0001249	PMID:30500825	PCS		8/8			P	HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000358	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619311	Hiatt-Neu-Cooper neurodevelopmental syndrome		HP:0000369	PMID:30500825	PCS					P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:270150	Sjogren syndrome		HP:0002960	OMIM:270150	IEA					P	HPO:iea[2009-02-17]
OMIM:270150	Sjogren syndrome		HP:0001970	OMIM:270150	TAS					P	HPO:skoehler[2015-12-30]
OMIM:270150	Sjogren syndrome		HP:0001370	OMIM:270150	IEA					P	HPO:iea[2009-02-17]
OMIM:270150	Sjogren syndrome		HP:0001939	OMIM:270150	IEA					P	HPO:iea[2009-02-17]
OMIM:270150	Sjogren syndrome		HP:0001097	OMIM:270150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270150	Sjogren syndrome		HP:0000217	OMIM:270150	IEA					P	HPO:iea[2009-02-17]
OMIM:270150	Sjogren syndrome		HP:0000007	OMIM:270150	IEA					I	HPO:iea[2009-02-17]
OMIM:612244	Inflammatory bowel disease 13		HP:0002037	OMIM:612244	IEA					P	HPO:skoehler[2013-01-09]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001276	PMID:22744658	PCS		4/14			P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0003676	PMID:22492559	PCS					C	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0000365	PMID:22492559	PCS		31/42			P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001272	PMID:22744658	PCS		14/14			P	HPO:skoehler[2012-12-03];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0002066	PMID:22492559	PCS					P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001252	PMID:22744658	PCS		4/14			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001251	PMID:22492559	PCS					P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0002380	PMID:22744658	PCS		8/14			P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0012473	PMID:22744658	PCS		13/14			P	HPO:skoehler[2013-11-28];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0000639	PMID:22744658	PCS		14/14			P	HPO:skoehler[2018-10-08];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0000514	PMID:22492559	PCS		24/39			P	HPO:skoehler[2013-02-25];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001308	PMID:22744658	PCS		10/14			P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001324	PMID:22744658	PCS		5/14			P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001347	PMID:22744658	TAS		14/14			P	HPO:skoehler[2012-10-17];HP:probinson[2019-03-03]
OMIM:614153	Spinocerebellar ataxia 36		HP:0000511	PMID:22492559	PCS		7/39			P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0002311	OMIM:614153	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614153	Spinocerebellar ataxia 36		HP:0003202	PMID:22744658	PCS		9/14			P	HPO:skoehler[2018-10-08];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0002015	PMID:22744658	PCS		6/14			P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0003445	PMID:22744658	IEA					P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0002078	PMID:22744658	PCS		14/14			P	HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0003487	PMID:22492559	PCS					P	HPO:skoehler[2013-02-25];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0001260	PMID:22744658;PMID:22492559	PCS		53/58			P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0002070	PMID:22744658	PCS		14/14			P	HPO:skoehler[2013-02-25];HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0000508	PMID:22492559	PCS		4/44			P	HP:probinson[2019-02-23]
OMIM:614153	Spinocerebellar ataxia 36		HP:0007772	OMIM:614153	TAS					P	HPO:skoehler[2012-12-03]
OMIM:614153	Spinocerebellar ataxia 36		HP:0000006	PMID:22744658	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0003621	PMID:26642243	PCS		5/11			C	HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0005764	PMID:26642243	PCS		5/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0000155	PMID:26642243	PCS		11/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0002583	PMID:26642243	PCS		2/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0003493	PMID:26642243	PCS		3/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0025343	PMID:26642243	PCS		3/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0003593	PMID:26642243	PCS		1/11			C	HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0032024	PMID:26642243	IEA		1/11			P	HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0002072	PMID:26642243	PCS		1/11			P	HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0012122	PMID:26642243	PCS		3/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0011463	PMID:26642243	PCS		4/11			C	HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0011462	PMID:26642243	PCS		1/11			C	HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0001878	PMID:26642243	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0001954	PMID:26642243	PCS		2/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0001888	PMID:26642243	PCS		2/11			P	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0000988	PMID:26642243	PCS		4/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0001873	PMID:26642243	PCS		1/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0000006	PMID:26642243	PCS					I	HPO:probinson[2017-06-17]
OMIM:616744	Autoinflammatory syndrome, familial, Behcet-like		HP:0003249	PMID:26642243	PCS		10/11			P	HPO:probinson[2017-06-17]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0003596	PMID:32467133	PCS		1/1			C	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0034045	PMID:32467133	PCS		1/1			P	HPO:probinson[2022-02-03]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0003551	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0003691	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0010984	PMID:32467133	PCS					I	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0012378	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0030319	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0003701	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0003547	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0011951	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:619477	Facioscapulohumeral muscular dystrophy 3, digenic		HP:0000467	PMID:32467133	PCS		1/1			P	HPO:probinson[2021-10-18]
OMIM:203800	Alstrom syndrome		HP:0001133	OMIM:203800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:203800	Alstrom syndrome		HP:0000164	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0003233	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000123	OMIM:203800	TAS				HP:0011010	P	HPO:skoehler[2013-06-06]
OMIM:203800	Alstrom syndrome		HP:0004322	PMID:34148947	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001970	PMID:21358663	PCS					P	HPO:probinson[2012-07-19]
OMIM:203800	Alstrom syndrome		HP:0000083	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0003074	PMID:34148947	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0010442	PMID:34148947	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0000639	PMID:34148947	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0000956	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000873	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0040217	PMID:34148947	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0007843	PMID:34148947	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0004438	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001763	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000831	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001644	OMIM:203800	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000572	OMIM:203800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:203800	Alstrom syndrome		HP:0002155	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000771	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001263	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000408	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000407	PMID:34148947	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0000007	OMIM:203800	IEA					I	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0005616	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0002621	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000842	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000523	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0002149	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001397	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0003577	PMID:34148947	PCS		1/1			C	HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0001596	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0002240	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000580	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000815	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000858	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000618	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000613	PMID:34148947	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0006532	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0200120	OMIM:203800	TAS					P	HPO:skoehler[2013-06-11]
OMIM:203800	Alstrom syndrome		HP:0002910	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0005987	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000230	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0002650	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0002099	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0002808	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000822	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001635	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000821	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000824	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000505	PMID:34148947	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:203800	Alstrom syndrome		HP:0000548	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001956	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0000388	OMIM:203800	IEA					P	HPO:iea[2009-02-17]
OMIM:203800	Alstrom syndrome		HP:0001513	PMID:34148947	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0003202	PMID:29449188	PCS		3/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0002136	OMIM:601238	TAS					P	HPO:probinson[2009-02-17]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0003577	PMID:14556008	PCS					C	HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0002078	PMID:14556008	PCS					P	HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0002067	PMID:29449188	PCS		3/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0000486	PMID:29449188	PCS		4/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001321	PMID:14556008	PCS					P	HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001332	PMID:29449188	PCS		2/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001272	PMID:29449188	PCS		5/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001260	PMID:14556008	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0002066	PMID:14556008;PMID:29449188	PCS		15/15			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-10-07];HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001252	PMID:14556008	PCS	HP:0003577				P	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001263	PMID:14556008	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001251	PMID:29449188	PCS		5/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0003593	PMID:29449188	PCS		5/5			C	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0002080	PMID:14556008	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0000639	PMID:14556008	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0000338	PMID:29449188	PCS		5/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0000007	PMID:14556008	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-07]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0001763	PMID:29449188	PCS		5/5			P	HPO:probinson[2024-03-09]
OMIM:601238	Cerebellar ataxia, Cayman type		HP:0000479	PMID:29449188	PCS		0/5			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-09]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0002069	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0002344	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0000572	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0002367	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0000992	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0001399	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0001288	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0002123	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0002186	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0002121	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0000709	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0100318	PMID:14663053	PCS					P	HPO:probinson[2019-09-23]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0000726	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0011165	OMIM:254780	TAS		20/20			P	HPO:skoehler[2017-07-13];HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0000007	OMIM:254780	IEA					I	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0007334	OMIM:254780	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0001336	OMIM:254780	IEA					P	HPO:iea[2009-02-17]
OMIM:254780	Myoclonic epilepsy of Lafora		HP:0003678	OMIM:254780	TAS					C	HPO:skoehler[2013-05-31]
OMIM:271500	Splenoportal vascular anomalies		HP:0000819	OMIM:271500	IEA				HP:0012825	P	HPO:probinson[2012-04-25]
OMIM:271500	Splenoportal vascular anomalies		HP:0001541	OMIM:271500	IEA					P	HPO:iea[2009-02-17]
OMIM:271500	Splenoportal vascular anomalies		HP:0005201	OMIM:271500	IEA					P	HPO:iea[2009-02-17]
OMIM:271500	Splenoportal vascular anomalies		HP:0001395	OMIM:271500	IEA					P	HPO:iea[2009-02-17]
OMIM:271500	Splenoportal vascular anomalies		HP:0001394	OMIM:271500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:271500	Splenoportal vascular anomalies		HP:0007111	OMIM:271500	IEA					P	HPO:iea[2009-02-17]
OMIM:271500	Splenoportal vascular anomalies		HP:0001987	OMIM:271500	IEA					P	HPO:iea[2009-02-17]
OMIM:271500	Splenoportal vascular anomalies		HP:0000007	OMIM:271500	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:271500	Splenoportal vascular anomalies		HP:0001744	OMIM:271500	IEA					P	HPO:iea[2009-02-17]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0001880	PMID:28111307;PMID:32750333	PCS		11/11			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0031813	PMID:32750333	PCS		1/1			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0001047	PMID:28111307;PMID:32750333	PCS		4/4		HP:0012828	P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0004322	PMID:28111307	PCS					P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0000100	PMID:32750333	PCS		1/1			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0002099	PMID:32750333	PCS		1/1			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0012578	PMID:32750333	PCS		1/1			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0001508	PMID:28111307;PMID:32750333	PCS		3/3			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0032021	PMID:28111307	PCS					P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0500093	PMID:28111307;PMID:32750333	PCS		11/11			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0000821	PMID:28111307	PCS					P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0001407	PMID:28111307	PCS	HP:0030674	2/2			P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0004429	PMID:28111307	PCS					P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0001433	PMID:28111307	PCS					P	HPO:probinson[2020-09-27]
OMIM:618999	Autoinflammation, immune dysregulation, and eosinophilia		HP:0000006	PMID:28111307	PCS					I	HPO:probinson[2020-09-27];HPO:probinson[2020-09-27]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0000341	PMID:31794024	PCS					P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0000252	PMID:31794024	PCS		7/7			P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0002650	PMID:31794024	PCS					P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0000343	PMID:31794024	PCS					P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0001250	PMID:31794024	PCS		7/7			P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0001272	PMID:31794024	PCS					P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0001263	PMID:31794024	PCS		7/7			P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0001285	PMID:31794024	IEA					P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0012444	PMID:31794024	PCS					P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0000407	PMID:31794024	PCS		2/6			P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0000007	PMID:31794024	PCS					I	HPO:probinson[2020-05-08];HPO:probinson[2022-05-15]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0008872	PMID:31794024	PCS	HP:0003623				P	HPO:probinson[2020-05-08]
OMIM:618741	Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy		HP:0003623	PMID:31794024	PCS		7/7			C	HPO:probinson[2022-05-15]
OMIM:607107	Nasopharyngeal carcinoma		HP:0010982	OMIM:607107	TAS					I	HPO:probinson[2013-03-02]
OMIM:607107	Nasopharyngeal carcinoma		HP:0100630	OMIM:607107	TAS					P	HPO:probinson[2013-01-09]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000286	PMID:29429572	PCS		2/7			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000486	PMID:29429572	PCS		2/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000365	PMID:29429572	PCS		4/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000243	PMID:29429572	PCS		1/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0004322	PMID:29429572	PCS		4/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0004442	PMID:29429572	PCS		2/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001252	PMID:29429572	PCS		4/7			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0011937	PMID:29429572	PCS		8/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0003593	PMID:29429572	PCS					C	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000280	PMID:29429572	PCS		2/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0011220	PMID:29429572	PCS		5/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000316	PMID:29429572	PCS		2/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001647	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000752	PMID:29429572	PCS		1/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0002019	PMID:29429572	PCS		6/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000358	PMID:29429572	PCS		3/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001249	PMID:29429572	PCS		7/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000494	PMID:29429572	PCS		6/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0009928	PMID:29429572	PCS		5/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000574	PMID:29429572	PCS		3/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0011968	PMID:29429572	PCS		5/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000691	PMID:29429572	PCS		2/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001263	PMID:29429572	PCS		8/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000767	PMID:29429572	PCS		2/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000403	PMID:29429572	PCS		4/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000722	PMID:29429572	PCS		1/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0004209	PMID:29429572	PCS		3/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000400	PMID:29429572	PCS		3/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000444	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000322	PMID:29429572	PCS		4/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000289	PMID:29429572	PCS		3/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000369	PMID:29429572	PCS		4/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000006	PMID:29429572	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000445	PMID:29429572	PCS		4/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001655	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000540	PMID:29429572	PCS		1/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001156	PMID:29429572	PCS		5/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000463	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001195	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001270	PMID:29429572	PCS		5/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0025162	PMID:29429572	PCS		2/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001629	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000733	PMID:29429572	PCS		2/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000219	PMID:29429572	PCS		4/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0002714	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000179	PMID:29429572	PCS		4/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000154	PMID:29429572	PCS		4/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001562	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0001561	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0000750	PMID:29429572	PCS		8/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0031936	PMID:29429572	PCS		6/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0005280	PMID:29429572	PCS		3/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0007099	PMID:29429572	PCS		1/8			P	HPO:probinson[2022-09-28]
OMIM:618027	Coffin-Siris syndrome 7		HP:0002209	PMID:29429572	PCS		6/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-28]
OMIM:600668	Chondrocalcinosis 1		HP:0000934	OMIM:600668	IEA					P	HPO:iea[2009-02-17]
OMIM:600668	Chondrocalcinosis 1		HP:0002758	OMIM:600668	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600668	Chondrocalcinosis 1		HP:0000006	OMIM:600668	IEA					I	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0002591	OMIM:275000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:275000	Graves disease		HP:0200028	OMIM:275000	IEA					P	HPO:skoehler[2009-02-17]
OMIM:275000	Graves disease		HP:0011788	OMIM:275000	TAS					P	HPO:probinson[2022-07-01]
OMIM:275000	Graves disease		HP:0000737	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0033077	OMIM:275000	TAS					P	HPO:probinson[2022-07-01]
OMIM:275000	Graves disease		HP:0031098	OMIM:275000	TAS					P	HPO:probinson[2022-07-01]
OMIM:275000	Graves disease		HP:0100647	OMIM:275000	IEA					P	HPO:skoehler[2015-01-27]
OMIM:275000	Graves disease		HP:0001806	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0001438	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0000007	OMIM:275000	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:275000	Graves disease		HP:0001635	OMIM:275000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:275000	Graves disease		HP:0000975	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0001824	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0000752	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0001324	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0000520	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0000853	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:275000	Graves disease		HP:0001347	OMIM:275000	IEA					P	HPO:iea[2009-02-17]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000396	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0007957	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0003577	PMID:25691407	IEA		1/1			C	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000260	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0005650	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000191	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0001060	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0100336	PMID:25691407	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0100337	PMID:25691407	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0009760	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0005807	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000007	PMID:25691407	PCS					I	HPO:probinson[2021-07-08];HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000568	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0009755	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0200055	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0009756	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000347	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000369	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619339	Popliteal pterygium syndrome, Bartsocas-Papas type 2		HP:0000269	PMID:25691407	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0003026	OMIM:615503	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0001561	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0002980	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0002089	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0001156	OMIM:615503	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0004322	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0000062	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0010454	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0005280	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0100732	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0100259	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0100258	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0001508	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0001629	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0000007	OMIM:615503	TAS					I	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0000774	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0001159	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0000256	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0000773	OMIM:615503	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615503	Short rib-polydactyly syndrome, type VI		HP:0006644	OMIM:615503	TAS					P	HPO:skoehler[2015-01-21]
OMIM:613172	Cardiomyopathy, dilated, 1DD		HP:0025169	PMID:35527250	PCS					P	HPO:probinson[2022-05-09]
OMIM:613172	Cardiomyopathy, dilated, 1DD		HP:0011462	PMID:35527250	PCS		3/3			C	HPO:probinson[2022-05-09]
OMIM:613172	Cardiomyopathy, dilated, 1DD		HP:0001635	PMID:35527250	PCS		0/5			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-05-09]
OMIM:613172	Cardiomyopathy, dilated, 1DD		HP:0000006	PMID:35527250	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-05-09]
OMIM:613172	Cardiomyopathy, dilated, 1DD		HP:0001645	PMID:35527250	PCS		1/5			P	HPO:probinson[2013-06-02];HPO:probinson[2022-05-09]
OMIM:613172	Cardiomyopathy, dilated, 1DD		HP:0001644	PMID:35527250	PCS		3/5			P	HPO:probinson[2013-06-02];HPO:probinson[2022-05-09]
OMIM:612278	Inflammatory bowel disease 19		HP:0002037	OMIM:612278	IEA					P	HPO:skoehler[2013-01-09]
OMIM:615517	Hemochromatosis, type 5		HP:0012463	PMID:11389486	PCS		1/1			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0010836	PMID:11389486	PCS		0/4			P	HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0012465	PMID:11389486	PCS		1/1			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0003452	PMID:11389486	PCS		1/1			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0001903	PMID:11389486	PCS		0/4			P	HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0003581	PMID:11389486	PCS		4/4			C	HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0032385	PMID:11389486	PCS		0/4			P	HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0033144	PMID:11389486	PCS		0/4			P	HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0003281	PMID:11389486	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615517	Hemochromatosis, type 5		HP:0000006	PMID:11389486	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:614609	Coffin-Siris syndrome 4		HP:0010803	PMID:25168959	PCS		4/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000365	PMID:25168959	PCS		4/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000343	PMID:25168959	PCS		3/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000463	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0004322	PMID:25168959	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001250	PMID:25168959	PCS		2/12			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001274	PMID:25168959	PCS		6/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001252	PMID:25168959	PCS		8/11			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000280	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0100368	PMID:25168959	PCS		12/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0002719	PMID:25168959	PCS		8/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001629	PMID:25168959	PCS	HP:0003577	3/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0011560	PMID:25168959	PCS	HP:0003577	1/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000998	PMID:25168959	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001305	OMIM:614609	TAS		1/6			P	HPO:probinson[2013-08-10]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000219	PMID:25168959	PCS		3/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0004935	PMID:25168959	PCS	HP:0003577	1/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000158	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001643	PMID:25168959	PCS		2/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0006237	PMID:25168959	PCS		3/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001642	PMID:25168959	PCS	HP:0003577	1/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000179	PMID:25168959	PCS		10/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001249	PMID:25168959	PCS		11/11			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000154	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000175	PMID:25168959	PCS		4/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000252	PMID:25168959	PCS		4/5			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001344	PMID:25168959	PCS		4/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0002650	PMID:25168959	PCS		5/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000574	PMID:25168959	PCS		9/12			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0009928	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000431	PMID:25168959	PCS		0/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0002750	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0011968	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001263	PMID:25168959	PCS		11/11			P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0005280	PMID:25168959	PCS		5/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000508	PMID:25168959	PCS		9/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0002209	PMID:25168959	PCS		5/12			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000527	PMID:25168959	PCS		10/12			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000505	PMID:25168959	PCS		5/11			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0009237	PMID:25168959	PCS		12/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001511	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614609	Coffin-Siris syndrome 4		HP:0001631	PMID:25168959	PCS	HP:0003577	1/12			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000322	PMID:25168959	PCS		5/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000006	PMID:25168959	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000446	PMID:25168959	PCS		2/11			P	HPO:probinson[2023-02-08]
OMIM:614609	Coffin-Siris syndrome 4		HP:0000445	OMIM:614609	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608220	Spastic paraplegia 25, autosomal recessive		HP:0002176	OMIM:608220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608220	Spastic paraplegia 25, autosomal recessive		HP:0000007	OMIM:608220	TAS					I	HPO:skoehler[2017-07-13]
OMIM:608220	Spastic paraplegia 25, autosomal recessive		HP:0003418	OMIM:608220	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608220	Spastic paraplegia 25, autosomal recessive		HP:0001258	OMIM:608220	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608220	Spastic paraplegia 25, autosomal recessive		HP:0030833	OMIM:608220	TAS					P	HPO:skoehler[2017-07-13]
OMIM:306950	Hernia, anterior diaphragmatic		HP:0003811	OMIM:306950	TAS					C	HPO:skoehler[2009-02-17]
OMIM:306950	Hernia, anterior diaphragmatic		HP:0000776	OMIM:306950	TAS					P	HPO:skoehler[2010-06-20]
OMIM:617300	Lymphatic malformation 7		HP:0002202	PMID:27400125	PCS		6/9			P	HPO:probinson[2023-03-07];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0003577	PMID:27400125	PCS		11/11			C	HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0001541	PMID:27400125	PCS		2/10			P	HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0000282	PMID:27400125	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0002098	PMID:27400125	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0001790	PMID:27400125	PCS		6/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0003270	OMIM:617300	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617300	Lymphatic malformation 7		HP:0010310	PMID:27400125	PCS		6/10			P	HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0100598	OMIM:617300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617300	Lymphatic malformation 7		HP:0000969	PMID:27400125	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0001903	PMID:27400125	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0010880	PMID:27400125	PCS	HP:0034199	2/11			P	HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0002619	PMID:27400125	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0001698	PMID:27400125	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0001631	PMID:27400125	PCS		6/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0001004	PMID:27400125	PCS		11/11			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-07]
OMIM:617300	Lymphatic malformation 7		HP:0000006	PMID:27400125	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-07]
OMIM:146300	Hypophosphatasia, adult		HP:0001760	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0000670	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0003282	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0003040	OMIM:146300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:146300	Hypophosphatasia, adult		HP:0002748	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0000007	OMIM:146300	IEA					I	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0002749	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0000934	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0002757	OMIM:146300	TAS					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0002659	OMIM:146300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0006323	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0006357	OMIM:146300	IEA					P	HPO:iea[2009-02-17]
OMIM:146300	Hypophosphatasia, adult		HP:0003239	PMID:35878747	PCS		59/59			P	HPO:probinson[2024-06-29]
OMIM:146300	Hypophosphatasia, adult		HP:0002756	OMIM:146300	TAS					P	HPO:skoehler[2010-06-20]
OMIM:146300	Hypophosphatasia, adult		HP:0000006	OMIM:146300	IEA					I	HPO:iea[2009-02-17]
OMIM:611771	Lipoprotein glomerulopathy		HP:0100820	PMID:18077821	PCS					P	HPO:probinson[2013-04-02]
OMIM:611771	Lipoprotein glomerulopathy		HP:0012574	PMID:10432380	PCS					P	HPO:probinson[2017-05-29]
OMIM:611771	Lipoprotein glomerulopathy		HP:0000083	PMID:18077821	PCS					P	HPO:probinson[2013-04-02]
OMIM:611771	Lipoprotein glomerulopathy		HP:0000093	PMID:18077821	PCS					P	HPO:probinson[2013-04-02]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000286	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0002024	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0004322	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000463	OMIM:242860	TAS					P	HPO:probinson[2012-05-01]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0010808	OMIM:242860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0003496	OMIM:242860	TAS					P	HP:probinson[2019-03-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0003196	OMIM:242860	TAS		20/20			P	HPO:probinson[2012-05-01];HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0012368	OMIM:242860	TAS					P	HPO:skoehler[2013-10-22]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0001508	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000316	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000158	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0001249	OMIM:242860	TAS					P	HPO:probinson[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0040218	OMIM:242860	TAS					P	HP:probinson[2019-03-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0002014	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0005403	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0002110	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000272	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0002090	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0005280	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000007	PMID:10588719	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000246	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000347	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0000369	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0002720	OMIM:242860	TAS					P	HP:probinson[2019-03-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0004469	OMIM:242860	IEA					P	HPO:iea[2009-02-17]
OMIM:242860	Immunodeficiency-Centromeric instability-facial anomalies syndrome		HP:0002721	OMIM:242860	IEA					P	HPO:skoehler[2015-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0000396	PMID:28054444	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0000143	PMID:28054444	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0000076	PMID:28054444	PCS		2/5			P	HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0002023	PMID:28054444	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0002650	PMID:28054444	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0003298	PMID:28054444	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0008551	PMID:28054444	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0000136	PMID:28054444	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0004736	PMID:28054444	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0000378	PMID:28054444	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0000047	PMID:28054444	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:617466	Townes-Brocks syndrome 2		HP:0000006	PMID:28054444	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0000939	PMID:23643382	PCS					P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0003621	PMID:23643382	PCS					C	HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0000365	PMID:23643382	PCS					P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0000938	PMID:23643382	PCS					P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0004409	PMID:23643382	PCS					P	HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0010983	PMID:23643382	PCS					I	HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0410030	PMID:23643382	PCS					P	HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0000823	PMID:23643382	PCS					P	HPO:probinson[2022-03-07]
OMIM:615271	Hypogonadotropic hypogonadism 21 with or without anosmia		HP:0000006	PMID:23643382	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0002421	PMID:22040219	PCS		1/1			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0008936	PMID:22040219	PCS		1/1			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0001276	PMID:11095995;PMID:22040219	PCS		4/4			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0002069	PMID:11095995	PCS		3/3			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0003643	PMID:22040219	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0002123	PMID:22040219	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0001321	PMID:22040219	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0002197	PMID:22040219	PCS		1/1			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0011968	PMID:22040219	PCS		1/1			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0003166	PMID:22040219	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0003570	PMID:11095995	PCS		1/1			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0001290	PMID:22040219	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0011344	PMID:11095995	PCS		3/3			P	HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0012110	PMID:22040219	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0500152	PMID:22040219	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0000817	PMID:22040219	PCS		1/1			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0002509	PMID:22040219	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0500181	PMID:22040219	PCS		1/1			P	HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0000007	PMID:11095995	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0003811	PMID:11095995	PCS		3/3			C	HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0003537	PMID:22040219	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0002126	PMID:22040219	PCS		1/1			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0003623	PMID:11095995;PMID:22040219	PCS		4/4			C	HPO:probinson[2022-04-11]
OMIM:615501	Molybdenum cofactor deficiency, complementation group C		HP:0001347	PMID:11095995	PCS		3/3			P	HPO:skoehler[2015-08-30];HPO:probinson[2022-04-11]
OMIM:110150	Blepharoptosis, myopia, and ectopia lentis		HP:0007970	OMIM:110150	TAS					P	HPO:skoehler[2009-02-17]
OMIM:110150	Blepharoptosis, myopia, and ectopia lentis		HP:0001083	OMIM:110150	IEA					P	HPO:iea[2009-02-17]
OMIM:110150	Blepharoptosis, myopia, and ectopia lentis		HP:0000006	OMIM:110150	IEA					I	HPO:iea[2009-02-17]
OMIM:110150	Blepharoptosis, myopia, and ectopia lentis		HP:0000545	OMIM:110150	IEA					P	HPO:iea[2009-02-17]
OMIM:110150	Blepharoptosis, myopia, and ectopia lentis		HP:0007800	OMIM:110150	TAS					P	HPO:probinson[2013-04-01]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0005650	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0002162	OMIM:609128	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0010326	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0100500	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0008110	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000639	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000938	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000954	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000059	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000473	OMIM:609128	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0002650	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0001762	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0005684	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000294	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0005280	OMIM:609128	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0012385	PMID:3565478	PCS	HP:0003577				P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0100499	OMIM:609128	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0002808	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0008589	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0004626	OMIM:609128	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000267	OMIM:609128	TAS					P	HPO:skoehler[2017-07-13]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000006	PMID:3565478	PCS					I	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0000666	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:609128	Arthrogryposis, distal, type 4		HP:0001215	PMID:3565478	PCS					P	HPO:probinson[2017-06-23]
OMIM:608236	Slowed nerve conduction velocity, autosomal dominant		HP:0011096	OMIM:608236	PCS					P	HPO:probinson[2012-04-11]
OMIM:608236	Slowed nerve conduction velocity, autosomal dominant		HP:0003383	OMIM:608236	PCS					P	HPO:probinson[2012-04-11]
OMIM:608236	Slowed nerve conduction velocity, autosomal dominant		HP:0003581	OMIM:608236	PCS					C	HPO:probinson[2012-04-11]
OMIM:608236	Slowed nerve conduction velocity, autosomal dominant		HP:0000762	OMIM:608236	PCS					P	HPO:probinson[2012-04-11]
OMIM:608236	Slowed nerve conduction velocity, autosomal dominant		HP:0000006	OMIM:608236	PCS					I	HPO:probinson[2012-04-11]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0001265	OMIM:300489	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0003445	OMIM:300489	IEA					P	HPO:iea[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0003621	OMIM:300489	IEA					C	HPO:iea[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0001761	OMIM:300489	IEA					P	HPO:iea[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0003693	OMIM:300489	IEA					P	HPO:iea[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0000759	OMIM:300489	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0001419	OMIM:300489	IEA					I	HPO:iea[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0002460	OMIM:300489	IEA					P	HPO:iea[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0002936	OMIM:300489	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0002317	OMIM:300489	IEA					P	HPO:iea[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0007269	OMIM:300489	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300489	Spinal muscular atrophy, distal, X-linked 3		HP:0003677	OMIM:300489	IEA					C	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0004820	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0006801	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0002166	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001310	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0003487	OMIM:159550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001272	PMID:27259050	PCS					P	HPO:probinson[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001260	OMIM:159550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001251	PMID:27259050	PCS					P	HPO:probinson[2012-06-03]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0011448	OMIM:159550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001908	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0000639	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001903	PMID:27259050	PCS					P	HPO:probinson[2019-09-03]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0003828	OMIM:159550	TAS					M	HPO:skoehler[2017-07-13]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0002936	OMIM:159550	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0002317	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0000762	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001873	PMID:27259050	PCS					P	HPO:probinson[2019-09-03]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0000006	PMID:27259050	PCS					I	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001876	OMIM:159550	IEA					P	HPO:iea[2009-02-17]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0002500	PMID:27259050	TAS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:159550	Ataxia-Pancytopenia syndrome		HP:0001875	PMID:27259050	PCS					P	HPO:probinson[2019-09-03]
OMIM:605074	Renal cell carcinoma, papillary, 1, familial and somatic		HP:0001442	PMID:9140397	PCS					I	HPO:probinson[2020-07-20]
OMIM:605074	Renal cell carcinoma, papillary, 1, familial and somatic		HP:0003829	PMID:9140397	PCS					I	HPO:skoehler[2013-03-23];HPO:probinson[2020-07-20]
OMIM:605074	Renal cell carcinoma, papillary, 1, familial and somatic		HP:0006766	PMID:9140397	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-20]
OMIM:605074	Renal cell carcinoma, papillary, 1, familial and somatic		HP:0000006	PMID:9140397	PCS					I	HPO:skoehler[2013-03-23];HPO:probinson[2020-07-20]
OMIM:114450	Cancer, familial, with in vitro radioresistance		HP:0002664	OMIM:114450	IEA					P	HPO:iea[2009-02-17]
OMIM:114450	Cancer, familial, with in vitro radioresistance		HP:0000006	OMIM:114450	IEA					I	HPO:iea[2009-02-17]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000164	PMID:23643382	PCS		2/8			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-09-06]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000939	OMIM:615267	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000365	PMID:23643382	PCS		6/8			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-09-06]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0008197	PMID:23643382	PCS		7/8			P	HPO:probinson[2022-09-06]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000938	PMID:23643382	PCS		HP:0040283			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-09-06]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000458	PMID:23643382	PCS		8/8			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-09-06]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000007	PMID:23643382	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-06]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000135	PMID:23643382	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-09-06]
OMIM:615267	Hypogonadotropic hypogonadism 18 with or without anosmia		HP:0000006	PMID:23643382	PCS					I	HPO:skoehler[2015-01-21];HPO:probinson[2022-09-06]
OMIM:163800	Sick sinus syndrome 2		HP:0003577	OMIM:163800	IEA					C	HPO:iea[2009-02-17]
OMIM:163800	Sick sinus syndrome 2		HP:0001695	PMID:15123648	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0005110	OMIM:163800	IEA					P	HPO:iea[2009-02-17]
OMIM:163800	Sick sinus syndrome 2		HP:0031547	PMID:25145518	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0011463	PMID:25145518	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0011462	PMID:15123648	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0033992	PMID:25145518	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0001664	PMID:15123648	PCS		1/1			P	HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0004757	PMID:12750403;PMID:25145518	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0001645	PMID:17646576	PCS		0/7			P	HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0001688	PMID:12750403;PMID:17646576;PMID:15123648;PMID:25145518	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:iea[2009-02-17];HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0003621	PMID:17646576	PCS		7/7			C	HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0001663	PMID:15123648	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0011704	PMID:15123648	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0003584	PMID:12750403	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0011705	PMID:25145518	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0003581	PMID:12750403	PCS		1/1			C	HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0030682	OMIM:163800;PMID:25145518	PCS		6/14			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0010872	PMID:25145518	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0005184	PMID:17646576;PMID:15123648	PCS		1/8			P	HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0034306	PMID:25145518	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0031677	PMID:15123648	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0025708	PMID:15123648	PCS		1/1			C	HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0001712	OMIM:163800	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:163800	Sick sinus syndrome 2		HP:0001659	OMIM:163800	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:163800	Sick sinus syndrome 2		HP:0001279	PMID:12750403;PMID:15123648;PMID:25145518	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2022-07-09]
OMIM:163800	Sick sinus syndrome 2		HP:0001634	OMIM:163800;PMID:25145518	PCS		6/14			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:163800	Sick sinus syndrome 2		HP:0000006	PMID:12750403	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:134780	Femoral-facial syndrome		HP:0001177	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000286	PMID:28948695	PCS		8/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0001770	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0004686	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0004322	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0100490	PMID:28948695	PCS		5/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0003196	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0002020	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0003274	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000319	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0002937	PMID:28948695	PCS		10/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0008455	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000912	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000878	PMID:28948695	PCS		9/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0001841	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0003745	OMIM:134780	IEA					I	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0002414	PMID:28948695	PCS		3/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0001643	PMID:28948695	PCS		5/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000113	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0001642	PMID:28948695	PCS		3/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0001249	PMID:28948695	PCS		4/24			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0002974	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000175	PMID:28948695	PCS		58/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000054	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0001660	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0003041	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0033183	PMID:28948695	PCS		4/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000921	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000565	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0006467	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000369	PMID:28948695	PCS		20/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0005613	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0004689	OMIM:134780	TAS					P	HPO:probinson[2012-05-08]
OMIM:134780	Femoral-facial syndrome		HP:0004742	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000582	PMID:28948695	PCS		25/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0003577	PMID:28948695	PCS		92/92			C	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000343	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000023	PMID:28948695	PCS		7/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0003097	PMID:28948695	PCS		72/92			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0001274	PMID:28948695	PCS		4/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0005792	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0002084	PMID:28948695	PCS		2/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0001629	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0000219	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0002119	PMID:28948695	PCS		7/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000059	PMID:28948695	PCS		7/43			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0009800	PMID:28948695	PCS		39/83			H	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0002996	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0001622	PMID:28948695	PCS		19/74			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0002650	PMID:28948695	PCS		11/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0001762	PMID:28948695	PCS		40/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000430	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0001680	PMID:28948695	PCS		1/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000902	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0008465	OMIM:134780	IEA					P	HPO:iea[2009-02-17]
OMIM:134780	Femoral-facial syndrome		HP:0004704	OMIM:134780	TAS					P	HPO:probinson[2012-05-08]
OMIM:134780	Femoral-facial syndrome		HP:0001159	PMID:28948695	PCS		12/92			P	HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000028	PMID:28948695	PCS		10/38			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000347	PMID:28948695	PCS		60/92			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:134780	Femoral-facial syndrome		HP:0000104	PMID:28948695	PCS		5/92			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:613616	Hyperoxaluria, primary, type III		HP:0003159	PMID:20797690	TAS					P	HPO:probinson[2013-06-02]
OMIM:613616	Hyperoxaluria, primary, type III		HP:0008672	PMID:20797690	TAS					P	HPO:probinson[2013-06-02]
OMIM:613616	Hyperoxaluria, primary, type III		HP:6001009	PMID:26401545	PCS					P	HPO:probinson[2024-08-03]
OMIM:613616	Hyperoxaluria, primary, type III		HP:0000007	PMID:20797690	TAS					I	HPO:probinson[2013-06-02]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0004325	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0007957	PMID:25220016	PCS		2/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002345	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000486	PMID:25220016;PMID:31957011;PMID:27388694	PCS		5/10			P	HPO:probinson[2022-05-29];HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001773	PMID:27388694;PMID:22581936	PCS		13/13			P	HPO:probinson[2022-05-29];HPO:skoehler[2013-07-30];HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002188	PMID:22581936	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0009938	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0025460	PMID:27388694	PCS		22/22			P	HP:probinson[2019-01-19];HPO:probinson[2018-04-13]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001250	PMID:27388694;PMID:22581936;PMID:24651605	PCS		12/21			P	HPO:probinson[2022-05-29];HP:probinson[2019-01-19];HPO:probinson[2017-05-27]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012706	PMID:27388694	PCS		12/12			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001252	PMID:31957011;PMID:22581936;PMID:24651605	PCS		13/13			P	HPO:probinson[2022-05-29];HPO:skoehler[2014-11-26]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012708	PMID:27388694	PCS		12/12			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0003593	PMID:27388694	PCS		12/12			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0032794	PMID:31957011	PCS		3/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0031146	PMID:27388694	PCS		10/11			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0030978	PMID:27388694	PCS		7/9			P	HPO:probinson[2018-04-13]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000954	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000316	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000711	PMID:25220016	PCS		2/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012070	PMID:22581936	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0025458	PMID:27388694	PCS					P	HPO:probinson[2018-04-13]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001249	PMID:31957011	PCS		4/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0003348	PMID:31957011	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001265	PMID:24651605	PCS		6/8			P	HPO:probinson[2017-05-27]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000297	PMID:27388694	PCS		12/12			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000252	PMID:24651605	PCS		6/8			P	HPO:probinson[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000970	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0025455	PMID:27388694	PCS					P	HPO:probinson[2018-04-13]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0030980	PMID:27388694	PCS		12/12			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002151	PMID:31957011	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001263	PMID:27388694;PMID:22581936;PMID:24651605	PCS		21/21			P	HPO:probinson[2022-05-29];HP:probinson[2019-01-19];HPO:skoehler[2013-07-30]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0030906	PMID:27388694	PCS		10/11			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002072	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0011800	PMID:27388694	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0100022	PMID:25220016	PCS		2/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012069	PMID:22581936	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0031162	PMID:27388694	IEA		11/11			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000007	PMID:24651605	PCS					I	HPO:skoehler[2013-07-30]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002305	PMID:27388694	IEA					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000369	PMID:27388694	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000248	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001336	PMID:27388694	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000522	PMID:31957011;PMID:22581936;PMID:24651605	PCS		12/15			P	HPO:probinson[2017-06-19];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002487	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001310	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000463	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012804	PMID:31957011	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001271	PMID:25220016;PMID:31957011	PCS		14/14			P	HPO:probinson[2022-05-29];HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001395	PMID:31957011	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002240	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012448	PMID:24651605	TAS		1/2		HP:0012825	P	HPO:skoehler[2013-11-28]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000939	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012531	PMID:25220016	PCS					P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0007021	PMID:25220016	PCS		2/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0006254	PMID:24651605	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000975	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0001945	PMID:25220016	PCS					P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0008954	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0003448	PMID:25220016	PCS		2/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002910	PMID:31957011;PMID:24651605	PCS		8/11			P	HPO:probinson[2022-05-29];HPO:skoehler[2013-07-30]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002159	PMID:22581936	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000275	PMID:27388694	PCS					P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002650	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002098	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000194	PMID:27388694	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000350	PMID:27388694	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002171	PMID:22581936	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0010536	PMID:27388694	PCS		1/11			P	HP:probinson[2019-01-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0012520	PMID:22581936	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0033044	PMID:22581936	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000508	PMID:25220016;PMID:27388694	PCS		2/6		HP:0012825	P	HPO:probinson[2022-05-29];HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0009830	PMID:22581936;PMID:24651605	PCS		2/3			P	HPO:probinson[2022-05-29];HPO:skoehler[2013-07-30]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0200136	PMID:25220016	PCS		2/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0000307	PMID:27388694	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0200055	PMID:31957011;PMID:22581936	PCS		4/5			P	HPO:probinson[2022-05-29];HPO:skoehler[2013-07-30];HPO:probinson[2021-07-06];HPO:probinson[2022-05-29]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0002205	PMID:25220016	PCS		1/2			P	HPO:lccarmody[2017-06-19]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0004305	PMID:31957011;PMID:22581936;PMID:24651605	PCS		6/7			P	HPO:probinson[2022-05-29];HPO:skoehler[2013-07-30]
OMIM:615273	Congenital disorder of deglycosylation 1		HP:0003535	PMID:31957011	PCS		2/4			P	HPO:probinson[2022-05-29]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0001265	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0003378	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0003376	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0001761	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0003693	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0003484	OMIM:607677	TAS					P	HPO:probinson[2012-03-13]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0001284	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0002460	OMIM:607677	TAS					P	HPO:skoehler[2013-02-25]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0002936	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0003380	OMIM:607677	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607677	Charcot-Marie-Tooth disease, axonal, type 2I		HP:0000006	OMIM:607677	TAS					I	HPO:skoehler[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000341	PMID:20512159	PCS		1/7			P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0002188	PMID:20512159	PCS		3/7			P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0004322	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000463	PMID:20512159	PCS		1/7			P	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0000160	PMID:20512159	PCS		2/7			P	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0000482	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0001252	PMID:20512159	IEA		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0001274	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000939	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0012650	PMID:20512159	PCS		7/7			P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0001508	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000519	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0001845	OMIM:600118	TAS		HP:0040283			P	HPO:skoehler[2012-11-26]
OMIM:600118	Warburg micro syndrome 1		HP:0000998	PMID:20512159	PCS		2/7			P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0002219	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0001249	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0001347	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0002751	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0001320	PMID:20512159	PCS		3/7			P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0001264	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000252	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0002059	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000233	PMID:20512159	PCS					P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0000431	PMID:20512159	PCS		1/7			P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0002079	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0001321	PMID:20512159	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0001382	OMIM:600118	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600118	Warburg micro syndrome 1		HP:0000490	PMID:20512159	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0003241	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0100952	PMID:20512159	PCS		7/7			P	HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0000508	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000568	PMID:20512159	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0000007	PMID:20512159	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0000648	PMID:20512159	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-06]
OMIM:600118	Warburg micro syndrome 1		HP:0000400	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000347	OMIM:600118	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000028	OMIM:600118	IEA					P	HPO:iea[2009-02-17]
OMIM:600118	Warburg micro syndrome 1		HP:0000369	PMID:20512159	PCS		2/7			P	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0003236	PMID:19949034	PCS		14/14			P	HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0005115	PMID:19949034	PCS		5/14			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0000573	OMIM:611773	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0000083	PMID:19949034	PCS		5/14			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0000790	PMID:19949034	PCS		7/14			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0003394	PMID:19949034	PCS		14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0030880	PMID:19949034	PCS		6/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0032325	PMID:19949034	PCS		4/9			P	HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0000107	PMID:19949034	PCS		4/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0002518	PMID:19949034	PCS		5/9			P	HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0004944	PMID:19949034	PCS		5/9			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0001136	PMID:19949034	PCS		14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0000006	PMID:18160688	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-02]
OMIM:611773	Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps		HP:0001249	PMID:19949034	PCS		0/14			P	HPO:probinson[2023-04-02]
OMIM:618031	Corneal dystrophy, posterior polymorphous, 4		HP:0009918	OMIM:618031	TAS		HP:0040284			P	HPO:skoehler[2019-02-15];HP:probinson[2019-02-17]
OMIM:618031	Corneal dystrophy, posterior polymorphous, 4		HP:0007663	OMIM:618031	IEA				HP:0003680	P	HPO:skoehler[2019-02-15]
OMIM:618031	Corneal dystrophy, posterior polymorphous, 4		HP:0000006	OMIM:618031	IEA					I	HPO:skoehler[2019-04-18]
OMIM:617302	Optic atrophy 11		HP:0002487	PMID:27495975	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002465	PMID:27495975	PCS		1/3			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000365	PMID:27495975	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000486	PMID:27495975	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002188	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001310	PMID:27495975	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000540	PMID:27495975	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0004322	PMID:27495975	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001250	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001252	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001251	PMID:27495975	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0003593	PMID:27495975	PCS		4/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0010729	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0033685	PMID:27495975	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0010521	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001270	PMID:27495975	PCS		4/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0012444	PMID:27495975	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0012172	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001349	PMID:27495975	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002119	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000752	PMID:27495975	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0003448	PMID:27495975	PCS		1/3			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000256	PMID:27495975	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002019	PMID:27495975	PCS	HP:0003593	3/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001249	PMID:27495975	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001744	PMID:27495975	PCS		2/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000252	PMID:27495975	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001344	PMID:27495975	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002474	PMID:27495975	PCS		4/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001321	PMID:27495975	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002352	PMID:27495975	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001263	PMID:27495975	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002151	PMID:27495975	PCS		3/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0011800	PMID:27495975	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0008180	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0011196	PMID:27495975	PCS		1/3			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000609	PMID:27495975	PCS		4/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000646	PMID:27495975	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000007	PMID:27495975	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000648	PMID:27495975	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:617302	Optic atrophy 11		HP:0000505	PMID:27495975	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000400	PMID:27495975	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002546	PMID:27495975	PCS		1/3			P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0002305	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0007018	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0000545	PMID:27495975	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0001776	PMID:27495975	PCS		1/4			P	HPO:probinson[2023-02-27]
OMIM:617302	Optic atrophy 11		HP:0003557	PMID:27495975	PCS		1/1			P	HPO:probinson[2023-02-27]
OMIM:615515	Amyotrophic lateral sclerosis 19		HP:0003596	PMID:24119685	PCS		2/6			C	HPO:probinson[2022-06-16]
OMIM:615515	Amyotrophic lateral sclerosis 19		HP:0003584	PMID:24119685	PCS		4/6			C	HPO:probinson[2022-06-16]
OMIM:615515	Amyotrophic lateral sclerosis 19		HP:0000726	PMID:24119685	PCS		0/3			P	HPO:probinson[2022-06-16]
OMIM:615515	Amyotrophic lateral sclerosis 19		HP:0007354	PMID:24119685	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-06-16]
OMIM:615515	Amyotrophic lateral sclerosis 19		HP:0002505	PMID:24119685	PCS		6/6			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-06-16]
OMIM:615515	Amyotrophic lateral sclerosis 19		HP:0002747	PMID:24119685	PCS		2/6			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-06-16]
OMIM:615515	Amyotrophic lateral sclerosis 19		HP:0000006	PMID:24119685	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-06-16]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001298	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002421	PMID:24847004	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002169	PMID:24847004	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002188	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001332	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000540	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0003297	PMID:24847004;PMID:27940755	PCS		2/2			P	HPO:probinson[2023-07-09];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001250	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001272	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0034919	PMID:24847004	PCS		1/1			P	HPO:probinson[2023-07-18]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0034918	PMID:24847004	PCS		1/1			P	HPO:probinson[2023-07-18]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001252	PMID:24847004	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-01-04]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001252	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0003593	PMID:24847004	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001251	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002161	PMID:24847004;PMID:27940755	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19];HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:6000478	PMID:2332510	PCS					P	HPO:probinson[2024-04-03]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001508	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000639	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0100704	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000238	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002119	PMID:24847004;PMID:27940755	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19];HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001522	OMIM:616034	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0008315	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002415	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001942	PMID:24847004	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002311	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002059	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000252	PMID:24847004;PMID:27940755	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000496	OMIM:616034	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001266	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0030048	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002079	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0011968	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002033	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001263	PMID:24847004	PCS		1/1		HP:0012829	P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002151	PMID:24847004;PMID:27940755	PCS		2/2			P	HPO:probinson[2023-07-09];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0500208	PMID:24847004;PMID:27940755	PCS		2/2			P	HPO:probinson[2023-07-09];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002490	PMID:24847004	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0011150	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0034197	PMID:27940755	PCS		1/1			C	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0003819	PMID:24847004	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0007034	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000602	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000007	PMID:24847004	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0000648	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001511	PMID:27940755	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0001257	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:616034	2,4-dienoyl-CoA reductase deficiency		HP:0002445	PMID:24847004	PCS		1/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-19]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003015	PMID:25348816;PMID:30448303	PCS		3/3			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003577	PMID:25348816;PMID:30448303	PCS		3/3			C	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0001377	PMID:23824842	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0008905	PMID:25348816;PMID:30448303	PCS		3/3			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002980	PMID:30448303	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0001156	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0005257	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0001252	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0001373	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0004482	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0010047	PMID:23824842	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0100255	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0100864	PMID:23824842	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0010055	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0008873	PMID:30448303	PCS		2/2			P	HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003307	PMID:23824842;PMID:25348816	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002857	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0006610	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003502	PMID:23824842	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003865	PMID:30448303	PCS		2/2			P	HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002677	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003026	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0009826	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003025	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003300	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0031936	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0001382	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003021	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0003186	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002691	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0004592	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0011800	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0005280	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0011447	PMID:25348816;PMID:30448303	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0012385	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0006380	PMID:25348816	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0010044	PMID:23824842	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002808	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0000926	PMID:30448303	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0000888	PMID:30448303	PCS		2/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0000007	PMID:23824842	PCS					I	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0005619	PMID:23824842	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002944	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0001538	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002986	PMID:23824842;PMID:25348816;PMID:30448303	PCS		4/4			P	HPO:probinson[2022-04-24];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0007413	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:618019	Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly		HP:0002007	PMID:30448303	PCS		1/2			P	HPO:probinson[2022-04-24]
OMIM:610445	Night blindness, congenital stationary, autosomal dominant 1		HP:0007737	OMIM:610445	IEA					P	HPO:probinson[2012-04-04]
OMIM:610445	Night blindness, congenital stationary, autosomal dominant 1		HP:0001123	OMIM:610445	IEA					P	HPO:probinson[2012-04-04]
OMIM:610445	Night blindness, congenital stationary, autosomal dominant 1		HP:0011463	PMID:8358437	PCS		1/1			C	HPO:probinson[2022-08-06]
OMIM:610445	Night blindness, congenital stationary, autosomal dominant 1		HP:0007642	PMID:9888392	PCS		1/1			P	HPO:probinson[2012-04-04];HPO:probinson[2020-07-21];HPO:probinson[2022-08-06]
OMIM:610445	Night blindness, congenital stationary, autosomal dominant 1		HP:0000006	PMID:7846071	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2020-07-21]
OMIM:610445	Night blindness, congenital stationary, autosomal dominant 1		HP:0000654	OMIM:610445	IEA					P	HPO:probinson[2012-04-04]
OMIM:614623	Keratoconus 6		HP:0000563	OMIM:614623	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614623	Keratoconus 6		HP:0000006	OMIM:614623	TAS					I	HPO:skoehler[2012-10-17]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0001891	OMIM:226300	IEA					P	HPO:iea[2009-02-17]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0005214	OMIM:226300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0001894	PMID:28657829	PCS		2/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002024	PMID:28657829	PCS		11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002783	PMID:28657829	PCS		5/11			P	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002242	OMIM:226300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0003075	PMID:28657829	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002240	OMIM:226300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0003593	PMID:28657829	PCS		2/9			C	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0003073	PMID:28657829	PCS		10/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002719	OMIM:226300	IEA					P	HPO:skoehler[2019-04-18]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0001903	PMID:28657829	PCS		9/11			P	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0011463	PMID:28657829	PCS		5/9			C	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002639	PMID:28657829	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002014	PMID:28657829	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0004313	PMID:28657829	PCS		11/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0003621	PMID:28657829	PCS		2/9			C	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0001541	OMIM:226300	IEA					P	HPO:iea[2009-02-17]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002013	PMID:28657829	PCS		6/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002593	PMID:28657829	PCS		5/11			P	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0030243	PMID:28657829	PCS		2/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002829	PMID:28657829	PCS		2/11			P	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0000969	PMID:28657829	PCS		9/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0100759	PMID:28657829	PCS		5/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0007430	OMIM:226300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0000007	PMID:28657829	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0001217	OMIM:226300	IEA					P	HPO:iea[2009-02-17]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0000821	PMID:28657829	PCS		3/11			P	HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0001510	PMID:28657829	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002027	PMID:28657829	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:226300	Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy		HP:0002204	OMIM:226300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0003676	PMID:21221996	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000365	OMIM:122860	TAS					P	HPO:probinson[2012-04-30]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0004322	OMIM:122860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0005652	PMID:21221996	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0003034	OMIM:122860	TAS					P	HPO:probinson[2012-04-30]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0003155	PMID:21221996	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0003593	PMID:21221996;OMIM:122860	PCS		11/11			C	HPO:probinson[2023-01-23];HPO:skoehler[2012-10-17]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0011120	PMID:21221996	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000316	OMIM:122860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0001349	OMIM:122860	TAS					P	HPO:probinson[2012-04-30]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0002516	OMIM:122860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0002315	PMID:21221996	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000256	OMIM:122860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000431	OMIM:122860	TAS					P	HPO:skoehler[2013-08-11]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000452	PMID:21221996	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0003165	PMID:21221996	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0001085	PMID:21221996	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0005464	PMID:21221996	PCS		1/1			P	HPO:probinson[2012-04-30];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0004493	PMID:21221996	PCS		1/1			P	HPO:probinson[2012-04-30];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0011421	PMID:21221996	PCS		1/1			C	HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0005280	PMID:21221996	PCS		1/1			P	HPO:skoehler[2013-08-11];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000529	OMIM:122860	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000648	OMIM:122860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000900	OMIM:122860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000006	PMID:21221996	PCS					I	HPO:probinson[2012-04-30];HPO:probinson[2023-01-23]
OMIM:122860	Craniodiaphyseal dysplasia, autosomal dominant		HP:0000303	PMID:21221996	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:604356	Duane retraction syndrome 2		HP:0000486	PMID:18653847	PCS					P	HPO:probinson[2013-02-23];HPO:probinson[2020-05-04]
OMIM:604356	Duane retraction syndrome 2		HP:0000646	PMID:18653847	PCS					P	HPO:probinson[2013-02-23];HPO:probinson[2020-05-04]
OMIM:604356	Duane retraction syndrome 2		HP:0009921	PMID:18653847	PCS					P	HPO:probinson[2013-02-23];HPO:probinson[2020-05-04]
OMIM:604356	Duane retraction syndrome 2		HP:0000006	PMID:18653847	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-05-04]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0003577	PMID:32776697	PCS		4/7			C	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0002021	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001252	PMID:32776697	PCS	HP:0003577	7/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0030319	PMID:32776697	PCS		7/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0033725	PMID:32776697	PCS		2/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001508	PMID:32776697	PCS	HP:0003593	2/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0032341	PMID:32776697	PCS		2/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0011461	PMID:32776697	PCS		3/7			C	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0000514	PMID:32776697	PCS		3/14			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001308	PMID:32776697	PCS		2/7			P	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0007941	PMID:32776697	PCS		4/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001621	PMID:32776697	PCS		3/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001620	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0003403	PMID:32776697	PCS		4/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001320	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0002015	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001682	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0002059	PMID:32776697	PCS		1/7		HP:0012825	P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0002650	PMID:32776697	PCS		3/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0003388	PMID:32776697	PCS		2/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001260	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001284	PMID:32776697	PCS		6/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0006380	PMID:32776697	PCS		4/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001718	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0000007	PMID:32776697	PCS					I	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001558	PMID:32776697	PCS	HP:0011461	3/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0006466	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0002747	PMID:32776697	PCS		2/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0002987	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001612	PMID:32776697	PCS		2/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0001611	PMID:32776697	PCS		2/7			P	HPO:probinson[2021-10-16]
OMIM:619461	Myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive		HP:0003557	PMID:32776697	PCS		1/7			P	HPO:probinson[2021-10-16]
OMIM:222600	Diastrophic dysplasia		HP:0003577	PMID:34064542	PCS		12/12			C	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0008608	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0001234	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0000365	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0001052	PMID:34064542	PCS		3/12			P	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0003273	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0001076	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0003071	OMIM:222600	TAS					P	HPO:probinson[2013-04-14]
OMIM:222600	Diastrophic dysplasia		HP:0010723	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0009381	OMIM:222600	TAS					P	HPO:probinson[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0009465	OMIM:222600	TAS					P	HPO:probinson[2012-07-17]
OMIM:222600	Diastrophic dysplasia		HP:0001609	OMIM:222600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222600	Diastrophic dysplasia		HP:0002938	PMID:34064542	PCS		7/12			P	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0008873	PMID:34064542	PCS		12/12			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0002999	PMID:34064542	PCS		7/12			P	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0008434	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0002857	PMID:34064542	PCS		10/12			P	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0001249	PMID:34064542	PCS		0/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0003026	OMIM:222600	TAS					P	HPO:probinson[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0002751	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0000175	PMID:34064542	PCS		8/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0001762	PMID:34064542	PCS		7/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0002650	PMID:34064542	PCS		3/12			P	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0000331	PMID:34064542	PCS		9/12			P	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0004894	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0002176	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0001518	PMID:34064542	PCS		10/10			P	HPO:probinson[2022-09-06]
OMIM:222600	Diastrophic dysplasia		HP:0010582	OMIM:222600	TAS					P	HPO:probinson[2013-04-14]
OMIM:222600	Diastrophic dysplasia		HP:0002947	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0000007	OMIM:222600	IEA					I	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0008921	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:222600	Diastrophic dysplasia		HP:0006646	OMIM:222600	IEA					P	HPO:iea[2009-02-17]
OMIM:166950	Teratoma, ovarian		HP:0000006	OMIM:166950	TAS					I	HPO:probinson[2009-02-17]
OMIM:166950	Teratoma, ovarian		HP:0012226	OMIM:166950	TAS					P	HPO:probinson[2013-03-30]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0004325	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0025386	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000365	PMID:34211179	PCS		5/25			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000486	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001574	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001332	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0003196	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010841	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012469	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000518	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012471	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001609	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010296	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0100767	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000239	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000238	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0030185	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000637	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000752	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002019	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002415	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000995	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000478	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0003763	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001067	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000252	PMID:34211179	PCS		5/21			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0003764	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001344	PMID:34211179	PCS		4/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0032408	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000771	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000490	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002033	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0100021	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010674	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0031951	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0100022	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0100540	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0011096	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000924	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0008760	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0008762	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002705	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002307	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000520	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000006	PMID:34211179	PCS					I	HPO:probinson[2021-10-05];HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002027	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001276	PMID:34211179	PCS		4/22			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000341	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001397	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002521	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000582	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000463	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001271	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012448	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001270	PMID:34211179	PCS		23/27			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002080	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0100033	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012446	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0008071	PMID:34211179	PCS		1/29			H	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0100543	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000737	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000739	PMID:34211179	PCS		3/20			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000337	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0020221	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000733	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000612	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0008751	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002119	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000736	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000219	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000218	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001945	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002910	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002599	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002478	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002754	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000473	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0025232	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002136	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000750	PMID:34211179	PCS		26/27			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002650	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0008619	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002376	PMID:34211179	PCS		3/25			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002013	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002373	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010812	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0011229	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0100710	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002808	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0500093	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001438	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000348	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001954	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0025502	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002527	PMID:34211179	PCS		6/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0007018	PMID:34211179	PCS		12/22			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0004944	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000589	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0004942	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010529	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001250	PMID:34211179	PCS		9/24			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001252	PMID:34211179	PCS		8/22			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001010	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001251	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010522	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000280	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002180	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0031589	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0031987	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000716	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012393	PMID:34211179	PCS		3/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000319	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000718	PMID:34211179	PCS		4/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000717	PMID:34211179	PCS		4/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000712	PMID:34211179	PCS		8/22			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000316	PMID:34211179	PCS		3/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000954	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000437	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001647	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002857	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000713	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001249	PMID:34211179	PCS		21/24			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000952	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000572	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001264	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002510	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000054	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002353	PMID:34211179	PCS		6/14			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000574	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0030148	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001382	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0011968	PMID:34211179	PCS		4/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000293	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001263	PMID:34211179	PCS		28/28			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012378	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000729	PMID:34211179	PCS		6/21			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002904	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000723	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000722	PMID:34211179	PCS		3/22			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001659	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000048	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000289	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001257	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000322	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000047	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0007359	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000567	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0410018	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002169	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002167	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0010862	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012498	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001508	PMID:34211179	PCS		4/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002719	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001629	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000817	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0009884	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000414	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001626	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000411	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000378	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000256	PMID:34211179	PCS		4/21			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001348	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001000	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001762	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000431	PMID:34211179	PCS		4/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0002057	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000152	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000790	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0032988	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0012760	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000708	PMID:34211179	PCS		4/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000707	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001999	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001635	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001118	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000307	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0030051	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000823	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0003418	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001357	PMID:34211179	PCS		2/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000268	PMID:34211179	PCS		3/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000664	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001511	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000388	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0000300	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:619475	Developmental delay, impaired speech, and behavioral abnormalities		HP:0001513	PMID:34211179	PCS		1/29			P	HPO:probinson[2021-10-05]
OMIM:612520	Diabetes mellitus, insulin-dependent, 20		HP:0100651	PMID:9313763	IEA					P	HPO:probinson[2013-01-09]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0003236	PMID:17878207	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0011463	PMID:17878207	PCS		1/1			C	HPO:probinson[2023-02-04]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0003593	OMIM:613158	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0003560	OMIM:613158	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0000007	PMID:17878207	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0011712	PMID:17878207	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-04]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0001270	OMIM:613158	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0003712	PMID:17878207	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613158	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2		HP:0003701	PMID:17878207	PCS		1/1		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-04]
OMIM:115000	Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome		HP:0001663	PMID:33536282	PCS					P	HPO:probinson[2021-06-30]
OMIM:115000	Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome		HP:0031628	PMID:33536282	PCS					P	HPO:probinson[2021-06-30]
OMIM:115000	Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome		HP:0006696	PMID:14115011	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-30]
OMIM:115000	Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome		HP:0011664	PMID:33536282	PCS		2/46			P	HPO:probinson[2021-06-30]
OMIM:115000	Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome		HP:0001664	PMID:33536282	PCS		1/46			P	HPO:probinson[2021-06-30]
OMIM:115000	Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome		HP:0000006	PMID:33536282	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-30]
OMIM:115000	Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome		HP:0001645	PMID:33536282	PCS					P	HPO:probinson[2021-06-30]
OMIM:615529	Craniosynostosis 5, susceptibility to		HP:0001363	PMID:17651129	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-12]
OMIM:615529	Craniosynostosis 5, susceptibility to		HP:0000006	PMID:17651129	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2023-02-12]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0005403	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0002014	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0002155	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0001790	PMID:33712616	PCS	HP:0011461	3/3			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0030718	PMID:33712616	PCS	HP:0011461	3/3			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0011900	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0003281	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0010976	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0006270	PMID:33712616	PCS	HP:0011461	3/3			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0031382	PMID:32865517	PCS		0/1			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0001706	PMID:33712616	PCS	HP:0011461	3/3			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0031692	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0011461	PMID:33712616	PCS		3/3			C	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0000778	PMID:33712616	PCS	HP:0011461	3/3			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0000007	PMID:32865517	PCS					I	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0001723	PMID:33712616	PCS	HP:0011461	3/3			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0001945	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0001698	PMID:33712616	PCS	HP:0011461	3/3			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0003347	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0040218	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:619313	Immunodeficiency 80 with or without cardiomyopathy		HP:0002721	PMID:32865517	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:158100	Monophalangy of great toe		HP:0000924	OMIM:158100	IEA					P	HPO:iea[2009-02-17]
OMIM:158100	Monophalangy of great toe		HP:0000006	OMIM:158100	IEA					I	HPO:iea[2009-02-17]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000286	PMID:30224647	PCS		9/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000384	PMID:30224647	PCS		1/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0010804	PMID:30224647	PCS		3/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000365	PMID:30224647	PCS		1/15			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001773	PMID:30224647	PCS		3/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000463	PMID:30224647	PCS		4/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001250	PMID:30224647	PCS		1/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0002020	PMID:30224647	PCS		8/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001290	PMID:30224647	IEA		13/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000319	PMID:30224647	PCS		4/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0012450	PMID:30224647	PCS		9/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000954	PMID:30224647	PCS		4/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0002119	PMID:30224647	PCS					P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001769	PMID:30224647	PCS		1/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0002714	PMID:30224647	PCS		9/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001423	PMID:30224647	PCS					I	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000377	PMID:30224647	PCS		12/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000278	PMID:30224647	PCS		3/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001249	PMID:30224647	PCS		12/12			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001028	PMID:30224647	PCS		2/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000494	PMID:30224647	PCS		10/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0003764	PMID:30224647	PCS		2/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001344	PMID:30224647	PCS		6/13			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000750	PMID:30224647	PCS		16/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0004279	PMID:30224647	PCS		5/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000452	PMID:30224647	PCS		1/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0031936	PMID:30224647	PCS		16/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0011968	PMID:30224647	PCS		13/15			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0002395	PMID:30224647	PCS		8/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000490	PMID:30224647	PCS		2/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001263	PMID:30224647	PCS		16/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000470	PMID:30224647	PCS		3/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0012811	PMID:30224647	PCS		7/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0002191	PMID:30224647	PCS		10/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001181	PMID:30224647	PCS		1/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0100022	PMID:30224647	PCS		2/15			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0012385	PMID:30224647	PCS		2/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000708	PMID:30224647	PCS		9/14			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000826	PMID:30224647	PCS		1/11			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000506	PMID:30224647	PCS		11/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0001998	PMID:30224647	PCS	HP:0003623	14/16			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000268	PMID:30224647	PCS		1/16			P	HPO:probinson[2020-09-03]
OMIM:301032	Basilicata-Akhtar syndrome		HP:0000369	PMID:30224647	PCS		6/16			P	HPO:probinson[2020-09-03]
OMIM:120050	Coxsackievirus B3 susceptibility		HP:0004429	OMIM:120050	IEA					P	HPO:skoehler[2013-01-09]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0002322	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0001300	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0002067	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0000012	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0001332	OMIM:605909	TAS					P	HPO:probinson[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0002063	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0003593	OMIM:605909	IEA					C	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0002172	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0000716	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0000726	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0000739	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0000007	OMIM:605909	IEA					I	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0003677	OMIM:605909	IEA					C	HPO:iea[2009-02-17]
OMIM:605909	Parkinson disease 6, autosomal recessive early-onset		HP:0001347	OMIM:605909	IEA					P	HPO:iea[2009-02-17]
OMIM:313350	Split-Hand/foot malformation 2		HP:0001839	OMIM:313350	IEA					P	HPO:iea[2009-02-17]
OMIM:313350	Split-Hand/foot malformation 2		HP:0010049	OMIM:313350	IEA					P	HPO:iea[2009-02-17]
OMIM:313350	Split-Hand/foot malformation 2		HP:0006101	OMIM:313350	IEA					P	HPO:iea[2009-02-17]
OMIM:313350	Split-Hand/foot malformation 2		HP:0001171	OMIM:313350	IEA					P	HPO:iea[2009-02-17]
OMIM:313350	Split-Hand/foot malformation 2		HP:0001417	OMIM:313350	IEA					I	HPO:iea[2009-02-17]
OMIM:313350	Split-Hand/foot malformation 2		HP:0009803	OMIM:313350	IEA					P	HPO:iea[2009-02-17]
OMIM:248340	3MC syndrome 3		HP:0007957	PMID:28301481	PCS		1/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000365	OMIM:248340	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248340	3MC syndrome 3		HP:0004322	PMID:28301481	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000581	PMID:28301481	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000085	PMID:28301481	PCS	HP:0003577	1/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000316	PMID:28301481	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0030084	PMID:28301481	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000537	PMID:28301481	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000377	PMID:28301481	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0001249	OMIM:248340	IEA					P	HPO:iea[2009-02-17]
OMIM:248340	3MC syndrome 3		HP:0002974	PMID:28301481	PCS		2/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0001540	PMID:28301481	PCS		3/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0002553	PMID:28301481	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000175	PMID:28301481	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000054	PMID:28301481	PCS		1/3	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0030025	PMID:28301481	PCS		1/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0011968	PMID:28301481	PCS		1/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0001263	PMID:28301481	PCS		1/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000808	OMIM:248340	IEA					P	HPO:iea[2009-02-17]
OMIM:248340	3MC syndrome 3		HP:0100258	PMID:28301481	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000508	OMIM:248340	TAS					P	HPO:skoehler[2012-10-17]
OMIM:248340	3MC syndrome 3		HP:0000007	PMID:28301481	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000048	OMIM:248340	IEA					P	HPO:iea[2009-02-17]
OMIM:248340	3MC syndrome 3		HP:0001510	OMIM:248340	IEA					P	HPO:iea[2009-02-17]
OMIM:248340	3MC syndrome 3		HP:0000960	PMID:28301481	PCS		3/7			P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000204	PMID:28301481	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0000028	PMID:28301481	PCS		1/3	MALE		P	HPO:probinson[2020-08-09]
OMIM:248340	3MC syndrome 3		HP:0002006	OMIM:248340	IEA					P	HPO:skoehler[2010-06-20]
OMIM:621101	Perrault syndrome 7		HP:0008209	PMID:39701103	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0008619	PMID:39701103	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0001399	PMID:39701103	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0004322	PMID:39701103	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0001250	PMID:39701103	PCS		0/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0011969	PMID:39701103	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0001263	PMID:39701103	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0001251	PMID:39701103	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0002240	PMID:39701103	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0010464	PMID:39701103	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0012622	PMID:39701103	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0011463	PMID:39701103	PCS		2/2			C	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0008232	PMID:39701103	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0001943	PMID:39701103	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0000007	PMID:39701103	PCS					I	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0000479	PMID:39701103	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0001249	PMID:39701103	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0000786	PMID:39701103	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:621101	Perrault syndrome 7		HP:0003128	PMID:39701103	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-03]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0001770	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000343	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0002240	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0001290	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0010248	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000518	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0001508	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0001944	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0001943	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0002910	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000311	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0001942	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000358	PMID:30566640	PCS		1/1			P	HPO:probinson[2023-02-06]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0002015	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000252	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0004279	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0002151	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000470	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000407	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000926	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000508	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000007	PMID:30566640	PCS					I	HPO:probinson[2020-08-27];HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0001511	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000028	PMID:30566640	PCS		1/1			P	HPO:probinson[2020-08-27]
OMIM:618958	Combined oxidative phosphorylation deficiency 47		HP:0000369	PMID:30566640	PCS		1/1			P	HPO:probinson[2023-02-06]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000286	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000483	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002188	PMID:27087320	PCS		2/8			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000486	PMID:27087320	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000089	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0004322	PMID:27087320	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002384	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001250	PMID:27087320	PCS		2/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001252	PMID:27087320	PCS		4/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000041	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002020	PMID:27087320	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0003593	PMID:27087320	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0410030	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0033725	PMID:27087320	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0012110	PMID:27087320	PCS		1/8			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000319	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002938	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000316	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000954	PMID:27087320	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0007565	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001643	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000358	PMID:27087320	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0020206	PMID:27087320	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0003623	PMID:27087320	PCS		2/8			C	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000494	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001385	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0030303	PMID:27087320	IEA		1/8			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000252	PMID:27087320	PCS		2/9			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000098	PMID:27087320	PCS		2/9			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000453	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002079	PMID:27087320	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0011968	PMID:27087320	PCS		5/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000490	PMID:27087320	PCS		3/20			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001260	PMID:27087320	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002033	PMID:27087320	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001263	PMID:27087320	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000609	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000407	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000729	PMID:27087320	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001734	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000601	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000568	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000648	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0004209	PMID:27087320	PCS		2/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000047	PMID:27087320	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000006	PMID:27087320	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000369	PMID:27087320	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000325	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001655	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000187	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0003577	PMID:27087320	PCS		6/8			C	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0004467	PMID:27087320	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001792	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000582	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000463	PMID:27087320	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000221	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000581	PMID:27087320	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0012803	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0011240	PMID:27087320	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001629	PMID:27087320	PCS		4/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0006097	PMID:27087320	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0100704	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000414	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000659	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002119	PMID:27087320	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000218	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000256	PMID:27087320	PCS		2/9			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001320	PMID:27087320	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001561	PMID:27087320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000076	PMID:27087320	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002650	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0009908	PMID:27087320	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001285	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0003186	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0010772	PMID:27087320	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0011229	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0010535	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-09-03]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0011304	PMID:27087320	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0012168	PMID:27087320	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-04-20];HPO:probinson[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0034295	PMID:27087320	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-04-20]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000107	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000349	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002007	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001511	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0001159	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0007018	PMID:27087320	PCS		2/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000589	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000028	PMID:27087320	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0002247	PMID:27087320	PCS		1/10			P	HPO:probinson[2019-08-29]
OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		HP:0000347	PMID:27087320	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-08-29]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0031834	PMID:30232381	PCS	HP:0011463				P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0011590	PMID:30232381	PCS	HP:0003577				P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0000716	PMID:30232381	PCS		4/9			P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0005134	PMID:30232381	PCS	HP:0003577				P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0012020	PMID:30232381	PCS	HP:0003577				P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0000739	PMID:30232381	PCS		4/9			P	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0001636	PMID:30232381	PCS	HP:0003577				P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0004935	PMID:30232381	PCS	HP:0003577				P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0001642	PMID:30232381	PCS	HP:0003577				P	HPO:probinson[2020-05-10]
OMIM:618780	Congenital heart defects, multiple types, 7		HP:0000006	PMID:30232381	PCS					I	HPO:probinson[2020-05-10];HPO:probinson[2020-05-10]
OMIM:136140	Floating-Harbor syndrome		HP:0000121	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000486	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0004322	PMID:22265015	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0003593	PMID:23763483	PCS		1/1			C	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0010047	PMID:22265015	PCS		2/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0012871	PMID:22265015	PCS		1/13			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0010252	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000718	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000878	PMID:22265015	PCS		2/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000358	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0001249	PMID:23763483;PMID:22265015	PCS		7/14			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0001007	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0002751	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0001385	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0030424	PMID:22265015	PCS		1/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0002474	PMID:22265015	PCS		13/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0010957	PMID:22265015	PCS		1/13			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0005301	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0002750	PMID:22265015	PCS		12/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0001382	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0000490	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0000691	PMID:22265015	PCS		2/5			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0003083	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000807	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0001537	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0009577	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000448	PMID:22265015	PCS		13/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000403	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000527	PMID:22265015	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000405	PMID:22265015	PCS		2/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0004209	PMID:23763483;PMID:22265015	PCS		9/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000322	PMID:23763483;PMID:22265015	PCS		12/14			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000047	PMID:22265015	PCS		1/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000325	PMID:22265015	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000369	PMID:22265015	PCS		9/13			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000006	PMID:22265015	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000126	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000023	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000540	PMID:22265015	PCS		2/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0001156	PMID:22265015	PCS		9/12			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0004220	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0002162	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0011599	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0010034	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0010230	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0000414	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000219	PMID:23763483;PMID:22265015	PCS		10/14			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0009765	PMID:23763483;PMID:22265015	PCS		14/14			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0002714	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0000894	PMID:22265015	PCS		1/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000154	PMID:22265015	PCS		12/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000670	PMID:22265015	PCS		3/5			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0004554	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000750	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0001047	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000430	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0031936	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0005487	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000470	OMIM:136140	IEA					P	HPO:iea[2009-02-17]
OMIM:136140	Floating-Harbor syndrome		HP:0001680	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0011300	PMID:22265015	PCS		7/9			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0011304	PMID:22265015	PCS		7/10			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0002608	PMID:22265015	PCS		1/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000426	PMID:23763483	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0001631	PMID:22265015	PCS		1/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:136140	Floating-Harbor syndrome		HP:0000028	PMID:22265015	PCS		1/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-27]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0003026	PMID:25492405	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0003774	PMID:25492405	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0002650	PMID:25492405	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0004322	PMID:25492405	PCS		1/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0001156	PMID:25492405	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0000007	PMID:21258341	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0001407	PMID:25492405	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0010442	PMID:25492405	PCS	HP:0003577	1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-17]
OMIM:613819	Short-Rib thoracic dysplasia 4 with or without polydactyly		HP:0000774	PMID:25492405	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-17]
OMIM:301026	Keipert syndrome		HP:0000486	PMID:30982611	PCS		2/10			P	HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0001156	PMID:30982611	PCS		5/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0002263	PMID:30982611	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0001382	PMID:30982611	PCS		2/10			P	HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0011800	PMID:30982611	PCS		7/9			P	HPO:skoehler[2019-09-07]
OMIM:301026	Keipert syndrome		HP:0011304	PMID:30982611	PCS		5/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0012385	PMID:30982611	PCS		3/9			P	HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0010055	PMID:30982611	PCS		7/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0000407	PMID:30982611	PCS		3/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0001419	PMID:30982611	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0011220	PMID:30982611	PCS		7/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0000316	PMID:30982611	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0000448	PMID:30982611	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0001802	PMID:30982611	PCS		1/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0030084	PMID:30982611	PCS		5/9			P	HPO:skoehler[2019-09-07]
OMIM:301026	Keipert syndrome		HP:0002714	PMID:30982611	PCS		7/9			P	HPO:skoehler[2019-09-07]
OMIM:301026	Keipert syndrome		HP:0007687	PMID:30982611	PCS		1/10			P	HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0000256	PMID:30982611	PCS		7/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0009836	PMID:30982611	PCS		7/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0001249	PMID:30982611	PCS		8/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0000369	PMID:30982611	PCS		5/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0000215	PMID:30982611	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:301026	Keipert syndrome		HP:0000445	PMID:30982611	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-21]
OMIM:602082	Corneal dystrophy of bowman layer, type II		HP:0001131	OMIM:602082	IEA					P	HPO:skoehler[2015-01-19]
OMIM:602082	Corneal dystrophy of bowman layer, type II		HP:0000613	OMIM:602082	IEA					P	HPO:iea[2009-02-17]
OMIM:602082	Corneal dystrophy of bowman layer, type II		HP:0000559	OMIM:602082	IEA					P	HPO:iea[2009-02-17]
OMIM:602082	Corneal dystrophy of bowman layer, type II		HP:0007755	OMIM:602082	IEA					P	HPO:iea[2009-02-17]
OMIM:602082	Corneal dystrophy of bowman layer, type II		HP:0000006	OMIM:602082	IEA					I	HPO:iea[2009-02-17]
OMIM:612291	Joubert syndrome 8		HP:0002883	PMID:25138100	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001276	PMID:25138100	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001344	PMID:25138100	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0031936	PMID:25138100	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0002085	PMID:18674751	PCS	HP:0003577	2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001252	PMID:18674751	PCS		4/4			P	HPO:probinson[2013-04-06];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001263	PMID:18674751	PCS		4/4			P	HPO:probinson[2013-04-06];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0000580	PMID:18674751	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0002240	PMID:25138100	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001251	PMID:25138100;PMID:18674751	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001290	PMID:18674751	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0000508	PMID:18674751	PCS		1/4			P	HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0000657	PMID:18674751	PCS		4/4			P	HPO:probinson[2013-04-06];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0002419	PMID:25138100;PMID:18674751	PCS		5/5			P	HPO:probinson[2021-01-30];HPO:probinson[2013-01-09];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0000007	PMID:18674751	PCS					I	HPO:probinson[2013-04-06]
OMIM:612291	Joubert syndrome 8		HP:0000543	PMID:25138100	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0006579	PMID:25138100	PCS		1/1			P	HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001513	PMID:25138100	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0001249	PMID:18674751	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-01-30]
OMIM:612291	Joubert syndrome 8		HP:0003623	PMID:25138100	PCS		1/1			C	HPO:probinson[2021-01-30]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0000044	PMID:15362570	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-28]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0000054	OMIM:614838	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0000175	OMIM:614838	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0000771	OMIM:614838	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0011803	PMID:17235395	PCS	HP:0003577	1/3			P	HPO:probinson[2023-01-28]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0410030	OMIM:614838	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0000939	OMIM:614838	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0000458	PMID:15362570	PCS		1/3			P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-28]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0004409	OMIM:614838	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0030084	PMID:15362570	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-28]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0008734	OMIM:614838	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0009921	PMID:17235395	PCS		1/3			P	HPO:probinson[2023-01-28]
OMIM:614838	Hypogonadotropic hypogonadism 9 with or without anosmia		HP:0000006	PMID:15362570	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-01-28]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0001771	PMID:35962790	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0033748	PMID:35962790	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0003577	PMID:35962790	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000486	PMID:35962790	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000023	PMID:35962790	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0001032	PMID:35962790	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0031006	PMID:35962790	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0200160	PMID:35962790	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000316	PMID:35962790	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0009884	PMID:35962790	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000678	PMID:35962790	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000218	PMID:35962790	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0003306	PMID:35962790	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0001249	PMID:35962790	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0002650	PMID:35962790	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0001762	PMID:35962790	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000034	PMID:35962790	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0006380	PMID:35962790	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0009130	PMID:35962790	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000508	PMID:35962790	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0006089	PMID:35962790	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000007	PMID:35962790	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0004209	PMID:35962790	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0006466	PMID:35962790	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0002942	PMID:35962790	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0005879	PMID:35962790	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000369	PMID:35962790	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0001634	PMID:35962790	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620545	Arthrogryposis, distal, type 12		HP:0000028	PMID:35962790	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300310	Immunodeficiency 61		HP:0002850	PMID:29636373	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:300310	Immunodeficiency 61		HP:0001419	PMID:29636373	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:300310	Immunodeficiency 61		HP:0003593	PMID:29636373	PCS		2/2			C	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:300310	Immunodeficiency 61		HP:0002718	PMID:29636373	PCS		2/2			P	HPO:probinson[2012-06-22];HPO:probinson[2023-02-11]
OMIM:300310	Immunodeficiency 61		HP:0000403	PMID:29636373	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-09]
OMIM:300310	Immunodeficiency 61		HP:0032138	PMID:29636373	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:300310	Immunodeficiency 61		HP:0002205	PMID:29636373	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11];HPO:probinson[2024-03-09]
OMIM:300310	Immunodeficiency 61		HP:0007018	PMID:29636373	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:300310	Immunodeficiency 61		HP:0008348	PMID:29636373	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:300310	Immunodeficiency 61		HP:0011108	PMID:29636373	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-03-09]
OMIM:300310	Immunodeficiency 61		HP:0001513	PMID:29636373	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001572	PMID:11228641	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0004841	PMID:11228641	PCS					P	HPO:probinson[2012-05-26]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0004322	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0011858	PMID:11228641	PCS					P	HPO:probinson[2012-05-26]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001250	PMID:11228641	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0010808	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0003593	PMID:11228641	PCS		3/3			C	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001290	PMID:11228641	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0012301	PMID:11228641	PCS		3/3			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001929	PMID:11228641	PCS					P	HPO:probinson[2012-05-26]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000718	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0008897	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0009623	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001763	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000278	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001007	OMIM:212066	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000358	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000494	OMIM:212066	TAS					P	HPO:skoehler[2012-11-20]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000252	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000574	OMIM:212066	TAS					P	HPO:skoehler[2013-01-22]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0002673	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000407	OMIM:212066	TAS					P	HPO:skoehler[2012-11-21]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000767	PMID:11228641	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000007	PMID:11228641	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001976	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000527	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000400	PMID:11228641	PCS		3/3			P	HPO:probinson[2013-08-11];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000444	PMID:11228641	PCS		2/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000248	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000369	PMID:11228641	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001276	OMIM:212066	IEA					P	HPO:skoehler[2018-10-08]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000343	PMID:11228641	PCS		2/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0008070	OMIM:212066	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001508	PMID:11228641	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001629	PMID:11228641	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000938	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001547	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000733	OMIM:212066;PMID:11228641	PCS		11/13			P	HPO:probinson[2023-04-09];HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0007466	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0002317	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0009765	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0012171	PMID:11228641	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0006610	PMID:11228641	PCS		2/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000212	PMID:11228641	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000256	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000699	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000154	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0003423	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000233	PMID:11228641	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000232	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0001321	PMID:11228641	PCS		0/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000194	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0003100	OMIM:212066	IEA					P	HPO:iea[2009-02-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000470	PMID:11228641	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0011344	PMID:11228641	PCS		3/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000426	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000303	PMID:11228641	PCS		1/3			P	HPO:probinson[2023-04-09]
OMIM:212066	Congenital disorder of glycosylation, type IIa		HP:0000742	OMIM:212066	TAS					P	HPO:skoehler[2012-10-17]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0000252	OMIM:616949	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0003388	OMIM:616949	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0100786	OMIM:616949	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0001250	PMID:24658003	PCS	HP:0011463				P	HPO:probinson[2017-06-25]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0001251	PMID:24658003	PCS					P	HPO:probinson[2017-06-25]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0002902	OMIM:616949	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0001290	OMIM:616949	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0000007	PMID:24658003	PCS					I	HPO:probinson[2017-06-25]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0011675	OMIM:616949	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0001249	PMID:24658003	PCS					P	HPO:probinson[2017-06-25]
OMIM:616949	Spinocerebellar ataxia, autosomal recessive 23		HP:0001875	OMIM:616949	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000483	OMIM:300476	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000541	OMIM:300476	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000551	PMID:16505158	PCS					P	HPO:probinson[2013-02-16]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0030825	OMIM:300476	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000639	OMIM:300476	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0001419	PMID:16505158	PCS					I	HPO:probinson[2013-01-09]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0008002	PMID:12807962	PCS					P	HPO:probinson[2013-02-16]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0008323	PMID:16505158	PCS					P	HPO:probinson[2013-02-16]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000613	OMIM:300476	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0007663	OMIM:300476	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000505	PMID:16505158	PCS					P	HPO:probinson[2013-02-16]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000603	PMID:12807962	PCS					P	HPO:probinson[2013-02-16]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000548	OMIM:300476	IEA					P	HPO:skoehler[2015-01-19]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000543	OMIM:300476	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:300476	Cone-Rod dystrophy, X-linked, 3		HP:0000545	PMID:12807962	PCS					P	HPO:probinson[2013-02-16]
OMIM:147791	Jacobsen syndrome		HP:0000286	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000486	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000243	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001371	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0002021	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000482	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0003196	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0010806	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001290	OMIM:147791	TAS					P	HPO:skoehler[2017-07-13]
OMIM:147791	Jacobsen syndrome		HP:0000316	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000238	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0003745	PMID:20520618	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:147791	Jacobsen syndrome		HP:0001249	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0005469	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000252	PMID:20520618	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:147791	Jacobsen syndrome		HP:0001263	PMID:20520618	PCS		2/2			P	HPO:probinson[2023-04-02]
OMIM:147791	Jacobsen syndrome		HP:0000646	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000921	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000767	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001734	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000568	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000648	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0004209	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000047	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001257	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000567	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000369	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0008947	OMIM:147791	IEA					P	HPO:skoehler[2010-06-18]
OMIM:147791	Jacobsen syndrome		HP:0000066	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000463	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001156	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000060	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001508	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001629	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000612	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000579	OMIM:147791	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147791	Jacobsen syndrome		HP:0000499	OMIM:147791	TAS					P	HPO:skoehler[2014-11-27]
OMIM:147791	Jacobsen syndrome		HP:0001104	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000256	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001360	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000470	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0005280	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000506	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000508	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000625	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001511	PMID:20520618	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:147791	Jacobsen syndrome		HP:0002205	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001631	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0001873	PMID:20520618	PCS		0/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:147791	Jacobsen syndrome		HP:0000028	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:147791	Jacobsen syndrome		HP:0000347	OMIM:147791	IEA					P	HPO:iea[2009-02-17]
OMIM:614186	Leber congenital amaurosis 16		HP:0000486	PMID:21763485	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0000662	PMID:21763485	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0001123	PMID:21763485	PCS		1/3			P	HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0000639	PMID:21763485	PCS	HP:0003577	3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0000518	PMID:21763485	PCS	HP:0011462	3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0003593	PMID:21763485	PCS		1/3			C	HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0000613	OMIM:614186	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614186	Leber congenital amaurosis 16		HP:0007663	PMID:21763485	PCS		3/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0000007	PMID:21763485	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-16]
OMIM:614186	Leber congenital amaurosis 16		HP:0000505	OMIM:614186	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614186	Leber congenital amaurosis 16		HP:0000543	OMIM:614186	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614186	Leber congenital amaurosis 16		HP:0003623	PMID:21763485	PCS		2/3			C	HPO:probinson[2023-02-16]
OMIM:615298	Symphalangism, proximal, 1B		HP:0009177	PMID:16127465	PCS					P	HPO:skoehler[2015-08-27];HPO:probinson[2020-05-04]
OMIM:615298	Symphalangism, proximal, 1B		HP:0006143	PMID:16127465	PCS					P	HPO:skoehler[2015-08-27];HPO:probinson[2020-05-04]
OMIM:615298	Symphalangism, proximal, 1B		HP:0004209	PMID:16127465	PCS					P	HPO:probinson[2020-05-04]
OMIM:615298	Symphalangism, proximal, 1B		HP:0001763	PMID:16892395	PCS					P	HPO:skoehler[2015-08-27];HPO:probinson[2020-05-04]
OMIM:615298	Symphalangism, proximal, 1B		HP:0009536	PMID:16127465	PCS					P	HPO:probinson[2020-05-04]
OMIM:615298	Symphalangism, proximal, 1B		HP:0000006	PMID:16127465	PCS					I	HPO:probinson[2020-05-04]
OMIM:173420	Platelet disorder, undefined		HP:0001892	OMIM:173420	IEA					P	HPO:iea[2009-02-17]
OMIM:173420	Platelet disorder, undefined		HP:0004377	OMIM:173420	TAS					P	HPO:skoehler[2009-02-17]
OMIM:173420	Platelet disorder, undefined		HP:0003540	OMIM:173420	IEA					P	HPO:iea[2009-02-17]
OMIM:173420	Platelet disorder, undefined		HP:0003010	OMIM:173420	IEA					P	HPO:iea[2009-02-17]
OMIM:173420	Platelet disorder, undefined		HP:0001873	OMIM:173420	IEA					P	HPO:iea[2009-02-17]
OMIM:173420	Platelet disorder, undefined		HP:0000006	OMIM:173420	IEA					I	HPO:iea[2009-02-17]
OMIM:173420	Platelet disorder, undefined		HP:0003006	OMIM:173420	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0009381	OMIM:604381	TAS					P	HPO:probinson[2012-06-10]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0001156	OMIM:604381	TAS					P	HPO:skoehler[2014-11-26]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0001647	OMIM:604381	TAS					P	HPO:probinson[2009-02-17]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0005295	OMIM:604381	TAS					P	HPO:probinson[2009-02-17]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0010047	OMIM:604381	TAS					P	HPO:probinson[2009-02-17]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0004209	OMIM:604381	TAS					P	HPO:probinson[2009-02-17]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0001643	OMIM:604381	TAS					P	HPO:probinson[2009-02-17]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0000006	OMIM:604381	TAS					I	HPO:probinson[2009-02-17]
OMIM:604381	Patent ductus arteriosus and bicuspid aortic valve with hand anomalies		HP:0001831	OMIM:604381	TAS					P	HPO:probinson[2012-06-10]
OMIM:613825	Complement component 9 deficiency		HP:0012308	OMIM:613825	TAS					P	HPO:probinson[2013-01-09]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0002169	PMID:26423925	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0001271	PMID:26423925	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0002066	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0030211	PMID:26423925	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000639	PMID:26423925	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0007340	PMID:26423925	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0011463	PMID:26423925	PCS		3/3			C	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000618	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0007663	PMID:26423925	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000510	PMID:26423925	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0001288	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0003487	PMID:26423925	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0002395	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0003484	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0002151	PMID:26423925	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0100321	PMID:26423925	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0034392	PMID:26423925	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0006380	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000407	PMID:26423925	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0001999	PMID:26423925	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000007	PMID:26423925	PCS					I	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0002967	PMID:26423925	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0002505	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0006466	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000543	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0001257	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0002987	PMID:26423925	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000762	PMID:26423925	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:621129	Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy 		HP:0000666	PMID:26423925	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-06]
OMIM:607850	Hand osteoarthritis		HP:0001387	OMIM:607850	TAS					P	HPO:probinson[2009-02-17]
OMIM:607850	Hand osteoarthritis		HP:0002829	OMIM:607850	TAS					P	HPO:probinson[2009-02-17]
OMIM:607850	Hand osteoarthritis		HP:0006233	OMIM:607850	TAS					P	HPO:probinson[2009-02-17]
OMIM:607850	Hand osteoarthritis		HP:0002758	OMIM:607850	TAS					P	HPO:probinson[2009-02-17]
OMIM:607850	Hand osteoarthritis		HP:0006226	OMIM:607850	TAS					P	HPO:probinson[2009-02-17]
OMIM:607850	Hand osteoarthritis		HP:0000006	OMIM:607850	TAS					I	HPO:probinson[2009-02-17]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0000750	PMID:32470375	PCS		4/6			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0000639	PMID:32470375	PCS		5/7			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0000729	PMID:32470375	PCS		5/6			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0001263	PMID:32470375	PCS					P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0001251	PMID:32470375	PCS		2/6			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0000739	PMID:32470375	PCS		1/6			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0000613	PMID:32470375	PCS		7/7			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0000007	PMID:32470375	TAS					I	HPO:probinson[2020-08-27];HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0007663	PMID:32470375	PCS		6/6			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0003074	PMID:32470375	PCS		3/4			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0000543	PMID:32470375	PCS		7/7			P	HPO:probinson[2020-08-27]
OMIM:618970	Cone-rod synaptic disorder syndrome, congenital nonprogressive		HP:0030329	PMID:32470375	PCS		4/4			P	HPO:probinson[2020-08-27]
OMIM:607688	Parkinson disease 11		HP:0002322	PMID:18358451	PCS					P	HPO:probinson[2013-03-04]
OMIM:607688	Parkinson disease 11		HP:0002067	PMID:18358451	PCS					P	HPO:probinson[2013-03-04]
OMIM:607688	Parkinson disease 11		HP:0002063	PMID:18358451	PCS					P	HPO:probinson[2013-03-04]
OMIM:607688	Parkinson disease 11		HP:0002172	PMID:18358451	PCS					P	HPO:probinson[2013-03-04]
OMIM:607688	Parkinson disease 11		HP:0002548	PMID:18358451	PCS					P	HPO:probinson[2013-03-04]
OMIM:607688	Parkinson disease 11		HP:0000006	PMID:18358451	PCS					I	HPO:probinson[2013-01-09]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0002751	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000252	PMID:34413497	PCS		6/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000486	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0002750	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0001156	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0002373	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0002099	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0001010	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000639	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000308	PMID:34413497	PCS		2/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000407	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000767	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000007	PMID:34413497	PCS					I	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0002967	PMID:34413497	PCS		2/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0004209	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000218	PMID:34413497	PCS		2/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000774	PMID:34413497	PCS		2/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000278	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0001138	PMID:34413497	PCS		2/6			P	HPO:probinson[2023-06-12]
OMIM:620237	Intellectual developmental disorder, autosomal recessive 78		HP:0000577	PMID:34413497	PCS		1/6			P	HPO:probinson[2023-06-12]
OMIM:121400	Cornea plana 1		HP:0000007	OMIM:121400	TAS					I	HPO:skoehler[2012-11-18]
OMIM:121400	Cornea plana 1		HP:0007720	OMIM:121400	IEA					P	HPO:iea[2009-02-17]
OMIM:121400	Cornea plana 1		HP:0000006	OMIM:121400	TAS					I	HPO:skoehler[2012-11-16]
OMIM:156850	Microphthalmia, isolated, with cataract 1		HP:0000486	OMIM:156850	IEA					P	HPO:iea[2009-02-17]
OMIM:156850	Microphthalmia, isolated, with cataract 1		HP:0000518	OMIM:156850	IEA					P	HPO:iea[2009-02-17]
OMIM:156850	Microphthalmia, isolated, with cataract 1		HP:0000639	OMIM:156850	IEA					P	HPO:iea[2009-02-17]
OMIM:156850	Microphthalmia, isolated, with cataract 1		HP:0000616	OMIM:156850	IEA					P	HPO:iea[2009-02-17]
OMIM:156850	Microphthalmia, isolated, with cataract 1		HP:0000568	OMIM:156850	IEA					P	HPO:iea[2009-02-17]
OMIM:156850	Microphthalmia, isolated, with cataract 1		HP:0000006	OMIM:156850	IEA					I	HPO:iea[2009-02-17]
OMIM:620551	Deafness, autosomal recessive 121		HP:0003577	PMID:37814107	PCS		4/5			C	HPO:probinson[2024-03-08]
OMIM:620551	Deafness, autosomal recessive 121		HP:0000407	PMID:37814107	PCS		5/5			P	HPO:probinson[2024-03-08]
OMIM:620551	Deafness, autosomal recessive 121		HP:0011463	PMID:37814107	PCS		1/5			C	HPO:probinson[2024-03-08]
OMIM:620551	Deafness, autosomal recessive 121		HP:0000007	PMID:37814107	PCS					I	HPO:probinson[2024-03-08]
OMIM:620551	Deafness, autosomal recessive 121		HP:0001756	PMID:37814107	PCS		0/5			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:620551	Deafness, autosomal recessive 121		HP:0000545	PMID:37814107	PCS		3/5			P	HPO:probinson[2024-03-08]
OMIM:168000	Paragangliomas 1		HP:0003334	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0006824	OMIM:168000	TAS					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0006748	PMID:15328326;PMID:12111639	PCS		27/49			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-15];HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0003596	PMID:15328326;PMID:12111639	PCS		14/49			C	HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0002640	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0008629	OMIM:168000	TAS					P	HPO:probinson[2016-07-22]
OMIM:168000	Paragangliomas 1		HP:0001609	OMIM:168000	TAS					P	HPO:probinson[2016-07-25]
OMIM:168000	Paragangliomas 1		HP:0011462	PMID:15328326;PMID:12111639	PCS		22/49			C	HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0000975	OMIM:168000	TAS					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0001649	OMIM:168000	TAS					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0001605	OMIM:168000	TAS					P	HPO:probinson[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0001962	OMIM:168000	TAS					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0001686	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0003621	PMID:15328326;PMID:12111639	PCS		9/49			C	HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0006737	PMID:15328326	PCS		12/24			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0006715	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0002331	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0003001	OMIM:168000	TAS					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0003584	PMID:15328326;PMID:12111639	PCS		4/49			C	HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0100635	PMID:12111639	PCS		2/25			P	HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0030074	OMIM:168000	TAS					P	HPO:skoehler[2015-01-20]
OMIM:168000	Paragangliomas 1		HP:0000405	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0000740	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0000006	PMID:12111639	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-15]
OMIM:168000	Paragangliomas 1		HP:0002886	OMIM:168000	IEA					P	HPO:iea[2009-02-17]
OMIM:168000	Paragangliomas 1		HP:0002864	PMID:15328326;PMID:12111639	PCS		6/49			P	HPO:probinson[2023-03-15]
OMIM:602096	Alzheimer disease 5		HP:0003584	OMIM:602096	TAS					C	HPO:skoehler[2009-02-17]
OMIM:602096	Alzheimer disease 5		HP:0000006	OMIM:602096	IEA					I	HPO:iea[2009-02-17]
OMIM:602096	Alzheimer disease 5		HP:0002511	OMIM:602096	TAS	HP:0003584				P	HPO:probinson[2014-04-22]
OMIM:612285	Joubert syndrome 9		HP:0003774	PMID:22241855	PCS		1/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0000483	OMIM:612285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612285	Joubert syndrome 9		HP:0002650	PMID:22241855	PCS		2/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0001250	PMID:22241855	PCS		5/20			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0001263	PMID:22241855	PCS		20/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0001395	PMID:22241855	PCS		1/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0002084	PMID:22241855	PCS		1/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0000518	OMIM:612285	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612285	Joubert syndrome 9		HP:0000639	PMID:22241855	PCS		13/19			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0100704	PMID:22241855	PCS		2/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0000657	PMID:22241855	PCS		13/19			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0000007	PMID:22241855	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0002419	PMID:22241855	PCS		20/20			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0002119	PMID:22241855	PCS		13/17			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0002876	PMID:22241855	PCS		12/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0001249	PMID:22241855	PCS		20/20			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0002104	PMID:22241855	PCS		12/20			P	HPO:probinson[2021-01-30]
OMIM:612285	Joubert syndrome 9		HP:0000556	PMID:22241855	PCS		2/20			P	HPO:probinson[2021-01-30]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0030502	PMID:1867553	PCS					P	HPO:skoehler[2015-07-26]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0007902	PMID:15937075	PCS		26/86			P	HPO:probinson[2017-05-28]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0000541	PMID:15937075	PCS		26/86			P	HPO:probinson[2009-02-17]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0000540	PMID:11384589	PCS					P	HPO:skoehler[2015-12-30]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0030824	PMID:1867553	PCS		4/4			P	HPO:probinson[2017-05-28]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0000529	PMID:15937075	PCS					P	HPO:probinson[2009-02-17]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0001419	OMIM:312700	TAS					I	HPO:skoehler[2019-04-18]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0000546	OMIM:312700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0007984	PMID:10922205	PCS					P	HPO:probinson[2009-02-17]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0007401	PMID:7662639	PCS		HP:0040282			P	HPO:probinson[2017-05-28]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0007722	PMID:7662639	PCS		HP:0040282			P	HPO:probinson[2017-05-28]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0007667	OMIM:312700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:312700	Retinoschisis 1, X-linked, juvenile		HP:0001105	OMIM:312700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0000175	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0100490	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0005011	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0002979	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0000007	OMIM:249710	IEA					I	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0006488	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0000278	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0004987	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:249710	Mesomelic limb shortening and bowing		HP:0000347	OMIM:249710	IEA					P	HPO:probinson[2012-07-30]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0001276	OMIM:154276	PCS					P	HPO:probinson[2009-02-17]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0002047	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0003236	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0003198	OMIM:154276	IEA					P	HPO:iea[2009-02-17]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0002153	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0011439	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0009045	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0011440	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0002905	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0001945	OMIM:154276	TAS					P	HPO:skoehler[2012-10-17]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0003558	OMIM:154276	PCS					P	HPO:probinson[2012-03-18]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0000006	OMIM:154276	TAS					I	HPO:skoehler[2015-12-30]
OMIM:154276	Malignant hyperthermia, susceptibility to, 3		HP:0003128	OMIM:154276	TAS					P	HPO:skoehler[2012-10-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0003577	PMID:8723097	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0001377	PMID:8723097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0001773	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0001552	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0001156	PMID:8723097	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0004322	PMID:8723097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0003370	PMID:8723097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0010049	PMID:8723097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0004180	PMID:8723097	PCS		1/1			P	HPO:iea[2012-06-10]
OMIM:271700	Spondyloperipheral dysplasia		HP:0010743	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0012106	PMID:8723097	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0010230	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0009882	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0006110	PMID:8723097	PCS		1/1			P	HPO:probinson[2012-06-10]
OMIM:271700	Spondyloperipheral dysplasia		HP:0009566	PMID:8723097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0000339	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0001169	OMIM:271700	TAS					P	HPO:probinson[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0002655	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0003301	PMID:8723097	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0003300	PMID:8723097	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0003022	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0005068	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0004991	PMID:8723097	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0000272	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0000470	PMID:8723097	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0011800	OMIM:271700	TAS					P	HPO:skoehler[2013-11-28]
OMIM:271700	Spondyloperipheral dysplasia		HP:0010454	PMID:8723097	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0011003	PMID:8723097	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0009290	PMID:8723097	PCS		1/1			P	HPO:iea[2012-06-10]
OMIM:271700	Spondyloperipheral dysplasia		HP:0003180	PMID:8723097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0005280	PMID:8723097	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0011304	OMIM:271700	TAS					P	HPO:probinson[2012-06-08]
OMIM:271700	Spondyloperipheral dysplasia		HP:0002808	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0000407	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0000926	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0006144	OMIM:271700	TAS					P	HPO:probinson[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0000768	OMIM:271700	IEA					P	HPO:iea[2009-02-17]
OMIM:271700	Spondyloperipheral dysplasia		HP:0009778	OMIM:271700	TAS					P	HPO:probinson[2012-06-08]
OMIM:271700	Spondyloperipheral dysplasia		HP:0000006	PMID:8723097	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:271700	Spondyloperipheral dysplasia		HP:0004227	PMID:8723097	PCS		1/1			P	HPO:iea[2012-06-10]
OMIM:271700	Spondyloperipheral dysplasia		HP:0001831	PMID:8723097	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000044	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000164	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0003431	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0004322	OMIM:604168	TAS					P	HPO:probinson[2012-04-11]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000482	PMID:14517542	PCS	HP:0003577				P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-12]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001251	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0003593	OMIM:604168	TAS					C	HPO:probinson[2012-04-11]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0010620	OMIM:604168	TAS					P	HPO:probinson[2012-04-11]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001270	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001171	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0007182	PMID:14517542	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0100543	OMIM:604168	TAS					P	HPO:skoehler[2014-04-04]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000815	OMIM:604168	TAS					P	HPO:skoehler[2013-07-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000639	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0002816	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0040078	OMIM:604168	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000519	PMID:14517542	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0008214	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0008734	OMIM:604168	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001249	OMIM:604168	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0002751	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0002059	PMID:14517542	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001762	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0003487	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001761	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001263	PMID:14517542	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0002072	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0011096	OMIM:604168	TAS					P	HPO:probinson[2012-04-11]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0001999	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0007178	OMIM:604168	TAS					P	HPO:probinson[2012-04-11]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000007	PMID:14517542	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0008942	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000764	OMIM:604168	IEA					P	HPO:iea[2009-02-17]
OMIM:604168	Congenital cataracts, facial dysmorphism, and neuropathy		HP:0000786	OMIM:604168	TAS		HP:0040283			P	HPO:skoehler[2013-07-17]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0003577	PMID:23236030	PCS		10/10			C	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0001374	PMID:23236030	PCS		9/9			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0004322	OMIM:615065	TAS					P	HPO:skoehler[2015-01-04]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000221	OMIM:615065	TAS					P	HPO:skoehler[2015-01-04]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000463	OMIM:615065	TAS					P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000160	PMID:23236030	PCS		3/10			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0003199	PMID:23236030	PCS		10/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0012473	PMID:23236030	PCS		7/7			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0001848	OMIM:615065	TAS		HP:0040283			P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000414	OMIM:615065	TAS					P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0003307	PMID:23236030	PCS		9/9			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000059	OMIM:615065	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000311	OMIM:615065	TAS					P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0002996	PMID:23236030	PCS		3/7			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0002553	OMIM:615065	TAS					P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000175	OMIM:615065	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0001762	OMIM:615065	TAS		HP:0040283			P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0002650	PMID:23236030	PCS		7/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000194	PMID:23236030	PCS		5/10			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0030001	PMID:23236030	PCS		1/10			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000470	PMID:23236030	PCS		10/10			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0001181	OMIM:615065	TAS					P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0012385	OMIM:615065	TAS				HP:0012825	P	HPO:skoehler[2013-10-22]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000508	PMID:23236030	PCS		7/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000007	PMID:23236030	PCS					I	HPO:skoehler[2013-03-08];HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0006201	PMID:23236030	PCS		4/8			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0006389	PMID:23236030	PCS		10/10			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0006467	PMID:23236030	PCS		2/8			P	HPO:probinson[2022-10-06]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0002987	OMIM:615065	TAS					P	HPO:skoehler[2013-03-08]
OMIM:615065	Arthrogryposis, distal, type 5D		HP:0000347	OMIM:615065	TAS					P	HPO:skoehler[2013-03-08]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0020072	PMID:24550228;PMID:25956530;PMID:25504528	PCS		7/7			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0031268	PMID:21796205	PCS		2/2			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0032218	PMID:25956530;PMID:21796205	PCS		3/3			P	HPO:probinson[2013-01-09];HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0100721	PMID:25956530	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0011462	PMID:25504528	PCS		1/2			C	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0012191	PMID:24550228	PCS	HP:0011462	4/4		HP:0033185	P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0002716	PMID:25956530	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0002837	PMID:25956530	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0001744	PMID:24550228	PCS		4/4			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0003621	PMID:25504528	PCS		1/2			C	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0005523	PMID:25504528	PCS		2/2		HP:0033185	P	HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0002110	PMID:25504528	PCS		1/2			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0032247	PMID:25956530	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0032204	PMID:21796205	PCS		2/2			P	HPO:probinson[2020-07-19];HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0011108	PMID:25956530;PMID:21796205	PCS		3/3			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0032170	PMID:24550228	PCS		1/4			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0012189	PMID:25956530	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0001419	PMID:21796205	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0033222	PMID:21796205;PMID:25504528	PCS		4/4			P	HPO:probinson[2020-12-07]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0000403	PMID:21796205	IEA		2/2			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0002848	PMID:25504528	PCS					P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0004429	PMID:21796205	PCS					P	HPO:probinson[2013-02-20]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0005419	PMID:21796205	PCS					P	HPO:probinson[2013-02-20]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0002205	PMID:25504528	PCS		1/2			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0001973	PMID:25956530	PCS		1/1			P	HPO:probinson[2020-11-27]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0002665	PMID:21796205	PCS					P	HPO:probinson[2013-02-20]
OMIM:300853	Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia		HP:0002721	PMID:21796205	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-11-27]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0004325	OMIM:617672	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002540	PMID:28777933	PCS		6/7			P	HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001332	PMID:28777933	PCS		4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001272	PMID:28777933	PCS		5/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002120	OMIM:617672	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001250	PMID:28777933	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002063	PMID:28777933	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001251	PMID:28777933	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0003593	PMID:28777933	PCS		3/7			C	HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002180	OMIM:617672	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0011463	PMID:28777933	PCS		4/7			C	HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001268	OMIM:617672	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0003447	OMIM:617672	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002059	PMID:28777933	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002015	OMIM:617672	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001300	PMID:28777933	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001344	PMID:28777933	PCS		7/7			P	HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002376	PMID:28777933	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002079	PMID:28777933	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0011968	OMIM:617672	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001263	PMID:28777933	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0005484	PMID:28777933	PCS		5/7			P	HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002072	PMID:28777933	PCS		1/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0002071	OMIM:617672	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0011096	OMIM:617672	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0030890	PMID:28777933	PCS		7/7			P	HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0007256	OMIM:617672	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0001257	PMID:28777933	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-04]
OMIM:617672	Neurodegeneration, childhood-onset, with brain atrophy		HP:0000006	PMID:28777933	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-04]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0000286	PMID:31155284	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001561	PMID:31155284	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0003577	PMID:31155284	PCS		2/2			C	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0005599	PMID:31155284	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0002188	PMID:31155284	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0004322	PMID:31155284	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0005565	PMID:31155284	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001272	PMID:31155284	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001010	PMID:31155284	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0002240	PMID:31155284	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001290	PMID:31155284	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0010862	PMID:31155284	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0002194	PMID:31155284	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0011002	PMID:31155284	PCS		0/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0000957	PMID:31155284	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0000316	PMID:31155284	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0000954	PMID:31155284	PCS		1/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0007663	PMID:31155284	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001511	PMID:31155284	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001510	PMID:31155284	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0000006	PMID:31155284	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001744	PMID:31155284	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618541	Hypopigmentation, organomegaly, and delayed myelination and development		HP:0001622	PMID:31155284	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0010958	PMID:33020172	PCS		2/2			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0003577	PMID:33020172	PCS		2/2			C	HPO:probinson[2022-07-09]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0002089	PMID:33020172	PCS		1/1			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0034198	PMID:33020172	PCS		1/2			C	HPO:probinson[2022-07-09]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0000007	PMID:33020172	PCS					I	HPO:probinson[2022-07-09]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0025700	PMID:33020172	PCS		1/1			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0002009	PMID:33020172	PCS		1/1			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:619887	Renal hypodysplasia/aplasia 4		HP:0002878	PMID:33020172	PCS		1/1			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:275200	Hypothyroidism, congenital, nongoitrous, 1		HP:0003577	PMID:7528344	PCS		3/3			C	HPO:probinson[2022-11-08]
OMIM:275200	Hypothyroidism, congenital, nongoitrous, 1		HP:0005990	PMID:7528344	PCS		0/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-08]
OMIM:275200	Hypothyroidism, congenital, nongoitrous, 1		HP:0000007	PMID:7528344	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:275200	Hypothyroidism, congenital, nongoitrous, 1		HP:0000821	PMID:7528344	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:275200	Hypothyroidism, congenital, nongoitrous, 1		HP:0002925	PMID:7528344	PCS	HP:0003577	3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-08]
OMIM:275200	Hypothyroidism, congenital, nongoitrous, 1		HP:0000853	PMID:7528344	PCS		0/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-11-08]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001771	PMID:27485408	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003577	PMID:27484770	PCS		2/2			C	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003236	PMID:30591934	TAS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0010628	PMID:27484770	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001371	PMID:30591934	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0000020	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003093	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0033008	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0010602	PMID:27484770	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0012473	PMID:27484770	PCS		2/2			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0002938	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0009027	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-07-16]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0025435	PMID:30591934	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001324	PMID:27484770;PMID:30591934;PMID:27485408	PCS		4/4			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003306	PMID:27484770	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0020203	PMID:27484770	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003326	PMID:27484770	PCS		2/2			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001265	PMID:27485408	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003202	PMID:27484770;PMID:30591934;PMID:27485408	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0002015	PMID:27484770	PCS		1/2			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0002650	PMID:30591934	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001762	PMID:30591934	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001288	PMID:27485408	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001761	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003044	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0001263	PMID:27484770	PCS		1/2			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0010677	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0000708	PMID:27484770	PCS		1/2			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0002607	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0002828	PMID:27484770	PCS		2/2			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0000007	PMID:27485408	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0002942	PMID:27484770	PCS		2/2			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0002987	PMID:27485408	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003798	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003677	PMID:27485408	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:617114	Myopathy, myofibrillar, 7		HP:0003557	PMID:27485408	PCS		1/1			P	HPO:probinson[2021-03-13]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0430043	PMID:30195269	PCS		3/3			P	HPO:probinson[2024-08-04]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000483	PMID:20503305	PCS		4/6			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000365	PMID:20503305	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000486	PMID:20503305	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000160	PMID:20503305	PCS	HP:0003593	4/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001252	OMIM:601776	TAS					P	HPO:skoehler[2014-11-26]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001373	PMID:20503305	PCS		4/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000482	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0003196	PMID:20503305	PCS		5/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001290	OMIM:601776	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000316	PMID:20503305	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-02];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000239	PMID:20503305	PCS		5/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002019	PMID:20503305	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001249	OMIM:601776	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000358	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0003623	PMID:20503305	PCS		3/6			C	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001540	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002036	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000175	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000494	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001382	PMID:26373698	PCS					P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-02]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001263	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001581	PMID:20503305	PCS		5/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002194	PMID:20503305	PCS		5/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001181	OMIM:601776	TAS				HP:0012828	P	HPO:probinson[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0012534	PMID:26373698	PCS					P	HPO:probinson[2021-05-02]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0005180	PMID:20503305	PCS		1/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0100699	OMIM:601776	TAS					P	HPO:skoehler[2012-11-18]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000767	PMID:20503305	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001537	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000007	PMID:20004762	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001659	PMID:20503305	PCS		2/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002107	PMID:20503305	PCS		3/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001653	PMID:20503305	PCS		2/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000248	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000369	PMID:20503305	PCS		5/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000324	PMID:20503305	PCS	HP:0003621	5/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000126	OMIM:601776	TAS				HP:0012832	P	HPO:skoehler[2013-06-06]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002246	OMIM:601776	TAS					P	HPO:skoehler[2012-11-19]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0003577	PMID:20503305	PCS		3/6			C	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000343	PMID:20503305	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000541	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002761	OMIM:601776	TAS					P	HPO:skoehler[2013-06-03]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000100	OMIM:601776	TAS					P	HPO:skoehler[2012-11-18]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001030	OMIM:601776	TAS					P	HPO:skoehler[2012-11-19]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002000	PMID:20503305	PCS		5/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001075	PMID:20503305	PCS		5/6			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0031364	OMIM:601776	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001270	OMIM:601776	TAS					P	HPO:skoehler[2012-11-18]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000337	OMIM:601776	TAS					P	HPO:skoehler[2012-11-19]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000978	PMID:20503305	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000219	PMID:20503305	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002119	OMIM:601776	TAS					P	HPO:skoehler[2012-11-18]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001704	PMID:20503305	PCS		1/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000218	PMID:20503305	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000411	OMIM:601776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000974	PMID:20503305	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001166	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000593	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000153	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002650	PMID:20503305	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-02];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001762	PMID:20503305	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000270	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0005684	OMIM:601776	TAS		20/20			P	HPO:skoehler[2012-11-18];HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000592	PMID:20503305	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000308	PMID:20503305	PCS	HP:0003593	4/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000506	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001999	OMIM:601776	IEA					P	HPO:iea[2009-02-17]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002804	OMIM:601776	TAS				HP:0012839	P	HPO:skoehler[2013-06-06]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001631	PMID:20503305	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000028	OMIM:601776	TAS		HP:0040281			P	HPO:skoehler[2012-11-18]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000501	PMID:20503305	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0002566	OMIM:601776	TAS					P	HPO:skoehler[2012-11-18]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0000545	PMID:20503305	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0001634	PMID:20503305	PCS		1/5			P	HPO:probinson[2022-08-10]
OMIM:601776	Ehlers-Danlos syndrome, musculocontractural type 1		HP:0004425	OMIM:601776	TAS					P	HPO:skoehler[2012-11-18]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0001397	PMID:24268657	IEA		11/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0003233	PMID:24268657	IEA		6/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0002155	PMID:24268657	IEA		4/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0003124	PMID:24268657	IEA		4/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0003141	PMID:24268657	IEA		2/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0005181	PMID:24268657	IEA		5/15		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0000822	PMID:24268657	IEA		11/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0001658	OMIM:615703	TAS					P	HPO:skoehler[2015-06-22]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0000789	OMIM:615703	TAS					P	HPO:skoehler[2015-06-22]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0000855	OMIM:615703	TAS					P	HPO:skoehler[2015-06-22]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0000007	PMID:24268657	IEA					I	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0001635	OMIM:615703	TAS					P	HPO:skoehler[2015-06-22]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0005978	PMID:24268657	IEA		3/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0001513	PMID:24268657	IEA		10/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0000798	PMID:24268657	IEA		6/6	MALE	HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0001249	PMID:24268657	IEA		3/11		HP:0012828	P	HPO:probinson[2015-05-10]
OMIM:615703	Morbid obesity and spermatogenic failure		HP:0000027	OMIM:615703	TAS					P	HPO:skoehler[2015-06-22]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001265	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0002861	OMIM:278730	IEA					P	HPO:skoehler[2018-10-08]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000252	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000992	PMID:9101292	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0003079	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0004334	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001266	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000491	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001251	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001097	OMIM:278730	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000518	OMIM:278730	IEA					P	HPO:skoehler[2018-10-08]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000407	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0011496	OMIM:278730	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000509	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000613	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001009	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000007	PMID:9101292	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000656	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000568	OMIM:278730	TAS					P	HPO:skoehler[2017-07-13]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001257	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001268	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001029	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0001249	OMIM:278730	PCS					P	HPO:probinson[2012-03-18]
OMIM:278730	Xeroderma pigmentosum, complementation group D		HP:0000621	OMIM:278730	IEA					P	HPO:iea[2009-02-17]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0003676	PMID:20593214	PCS					C	HPO:skoehler[2013-05-03];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0000365	OMIM:614409	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002166	OMIM:614409	TAS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0001272	PMID:20593214	PCS		2/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0000020	OMIM:614409	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002064	OMIM:614409	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002061	PMID:20593214	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0003690	OMIM:614409	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0000518	PMID:20593214	PCS	HP:0003577	4/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0000639	OMIM:614409	TAS					P	HPO:skoehler[2014-02-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0011463	PMID:20593214	PCS		3/5			C	HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0007340	PMID:20593214	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0001268	OMIM:614409	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0001249	OMIM:614409	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0001347	PMID:20593214	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002059	PMID:20593214	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002378	PMID:20593214	PCS		1/5			P	HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0003621	PMID:20593214	PCS		2/5			C	HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002650	PMID:20593214	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0003487	PMID:20593214	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002079	PMID:20593214	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002310	PMID:20593214	PCS		1/5			P	HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0001761	PMID:20593214	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0001260	PMID:20593214	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002495	PMID:20593214	PCS		1/5			P	HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0011449	OMIM:614409	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0011448	OMIM:614409	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0000726	PMID:20593214	PCS		5/5			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002808	OMIM:614409	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0000789	OMIM:614409	TAS		HP:0040283	MALE		P	HPO:skoehler[2013-06-03]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0008003	OMIM:614409	TAS					P	HPO:skoehler[2014-02-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0000007	PMID:20593214	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002406	OMIM:614409	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0020036	OMIM:614409	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0001258	PMID:20593214	PCS		5/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-11-06]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0002346	OMIM:614409	TAS		HP:0040283			P	HPO:skoehler[2013-05-03]
OMIM:614409	Spastic paraplegia 46, autosomal recessive		HP:0006986	PMID:20593214	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0000473	PMID:16525029	PCS		2/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0000484	PMID:16525029	PCS		1/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0008936	PMID:16525029	PCS		1/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0003577	PMID:16525029	PCS		1/2			C	HPO:probinson[2013-12-16];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0001321	OMIM:607313	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0007817	OMIM:607313	TAS					P	HPO:probinson[2014-01-04]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0001263	PMID:16525029	PCS		1/1			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0003593	PMID:16525029	PCS		1/2			C	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0001290	PMID:16525029	PCS		1/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0012110	PMID:16525029	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0000639	PMID:16525029	PCS		2/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0007650	OMIM:607313	TAS					P	HPO:probinson[2009-02-17]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0000634	PMID:16525029	PCS		1/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0000007	PMID:16525029	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0002944	PMID:16525029	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0025336	PMID:16525029	PCS		2/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0001357	PMID:16525029	PCS		1/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0000565	PMID:16525029	PCS		1/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1		HP:0000256	PMID:16525029	PCS		1/2			P	HPO:probinson[2022-11-02];HPO:probinson[2022-11-02]
OMIM:617100	Familial adenomatous polyposis 4		HP:0005227	PMID:27476653	PCS		4/4			P	HPO:probinson[2022-11-11];HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0000131	PMID:27476653	PCS		2/4			P	HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0003596	PMID:27476653	PCS		1/4			C	HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0009592	PMID:27476653	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0004783	PMID:27476653	PCS		1/4			P	HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0033770	PMID:27476653	PCS		1/4			P	HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:6000102	PMID:27476653	PCS		2/3			P	HPO:probinson[2024-01-06]
OMIM:617100	Familial adenomatous polyposis 4		HP:0011462	PMID:27476653	PCS		3/4			C	HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0000107	PMID:27476653	PCS		1/4			P	HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0000007	PMID:27476653	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0000854	PMID:27476653	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-11]
OMIM:617100	Familial adenomatous polyposis 4		HP:0000138	PMID:27476653	PCS		1/4			P	HPO:probinson[2022-11-11]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0002650	PMID:29100092	PCS		7/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0003311	OMIM:184255	TAS					P	HPO:probinson[2009-02-17]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0004322	PMID:29100092	PCS		8/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0003025	PMID:29100092	PCS		8/8			P	HPO:probinson[2012-05-26];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0002970	PMID:29100092	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0003300	PMID:29100092	PCS		5/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0100864	PMID:29100092	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0003908	PMID:29100092	PCS					P	HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0002515	OMIM:184255	TAS					P	HPO:probinson[2009-02-17]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0002812	PMID:29100092	PCS		3/9			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0000768	PMID:29100092	PCS		4/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0002657	PMID:29100092	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0004603	OMIM:184255	TAS					P	HPO:probinson[2009-02-17]
OMIM:184255	Spondylometaphyseal dysplasia, corner Fracture type		HP:0000006	PMID:29100092	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-04]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001298	OMIM:618233	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0003676	PMID:16200211	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001310	OMIM:618233	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001250	OMIM:618233	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001252	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001251	PMID:16200211	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0000639	PMID:16200211	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0011463	PMID:16200211	PCS		1/1			C	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0002878	PMID:16200211	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001265	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0002136	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0002015	PMID:16200211	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0011968	PMID:16200211	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0002352	OMIM:618233	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001263	PMID:16200211	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0001284	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0002490	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0011923	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0010535	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0007110	OMIM:618233	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0000007	PMID:16200211	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0000648	PMID:16200211	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0002104	OMIM:618233	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0000666	PMID:16200211	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618233	Mitochondrial complex I deficiency, nuclear type 10		HP:0000544	OMIM:618233	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:611571	Otosclerosis 4		HP:0000362	OMIM:611571	IEA					P	HPO:iea[2009-02-17]
OMIM:611571	Otosclerosis 4		HP:0000410	OMIM:611571	TAS					P	HPO:probinson[2012-07-25]
OMIM:611571	Otosclerosis 4		HP:0000006	OMIM:611571	IEA					I	HPO:iea[2009-02-17]
OMIM:167870	Panic disorder 1		HP:0000739	OMIM:167870	IEA					P	HPO:skoehler[2010-06-20]
OMIM:167870	Panic disorder 1		HP:0000006	OMIM:167870	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:601004	Portal vein, cavernous transformation of		HP:0004941	OMIM:601004	TAS					P	HPO:probinson[2009-02-17]
OMIM:601004	Portal vein, cavernous transformation of		HP:0000006	OMIM:601004	TAS					I	HPO:probinson[2009-02-17]
OMIM:617666	Fraser syndrome 2		HP:0025023	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0003577	PMID:15838507	PCS		4/4			C	HPO:probinson[2023-04-07];HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0002023	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000089	OMIM:617666	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617666	Fraser syndrome 2		HP:0000122	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000062	PMID:15838507	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000160	PMID:15838507	PCS		1/4			P	HPO:skoehler[2019-04-18]
OMIM:617666	Fraser syndrome 2		HP:0012725	PMID:15838507	PCS		3/4			P	HPO:skoehler[2019-04-18]
OMIM:617666	Fraser syndrome 2		HP:0003270	OMIM:617666	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617666	Fraser syndrome 2		HP:0010306	PMID:15838507	PCS		1/4			P	HPO:skoehler[2019-04-18]
OMIM:617666	Fraser syndrome 2		HP:0000778	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0002878	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0001126	PMID:15838507	PCS		3/4			P	HPO:skoehler[2019-04-18]
OMIM:617666	Fraser syndrome 2		HP:0000413	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0005349	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0001562	PMID:15838507	PCS		2/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0010958	PMID:15838507	PCS		2/4			P	HPO:probinson[2023-04-07];HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000430	PMID:15838507	PCS		1/4			P	HPO:skoehler[2019-04-18]
OMIM:617666	Fraser syndrome 2		HP:0000294	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000470	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0010477	PMID:15838507	PCS		3/4			P	HPO:skoehler[2019-04-18]
OMIM:617666	Fraser syndrome 2		HP:0012300	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000007	PMID:15838507	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000568	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0002566	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000369	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000104	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:617666	Fraser syndrome 2		HP:0000445	PMID:15838507	PCS		1/4			P	HPO:probinson[2023-04-07]
OMIM:618555	Night blindness, congenital stationary, type 1I		HP:0000662	PMID:29559409	PCS	HP:0011463	5/5			P	HPO:probinson[2020-07-22]
OMIM:618555	Night blindness, congenital stationary, type 1I		HP:0000552	PMID:29559409	PCS		2/5			P	HPO:probinson[2020-07-22]
OMIM:618555	Night blindness, congenital stationary, type 1I		HP:0000007	PMID:29559409	PCS					I	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:607475	Bothnia retinal dystrophy		HP:0000662	OMIM:607475	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607475	Bothnia retinal dystrophy		HP:0000608	OMIM:607475	IEA					P	HPO:iea[2009-02-17]
OMIM:607475	Bothnia retinal dystrophy		HP:0000007	OMIM:607475	IEA					I	HPO:iea[2009-02-17]
OMIM:607475	Bothnia retinal dystrophy		HP:0000512	OMIM:607475	IEA					P	HPO:iea[2009-02-17]
OMIM:607475	Bothnia retinal dystrophy		HP:0000556	OMIM:607475	TAS					P	HPO:skoehler[2015-01-21]
OMIM:615071	Alazami syndrome		HP:0004325	PMID:22865833	PCS		8/9			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0003510	PMID:22865833	PCS		9/9			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000154	PMID:22865833	PCS		9/9			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000252	PMID:22865833	PCS		4/9			P	HPO:skoehler[2013-06-12];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0002650	PMID:22865833	PCS		2/9			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000486	PMID:22865833	PCS		4/9			P	HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000431	OMIM:615071	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615071	Alazami syndrome		HP:0000490	PMID:22865833	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0001263	OMIM:615071	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615071	Alazami syndrome		HP:0000272	PMID:22865833	PCS		8/9			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0045025	PMID:22865833	PCS		7/9			P	HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0012646	PMID:22865833	PCS		1/5			P	HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0012745	PMID:22865833	PCS		7/9			P	HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0005280	OMIM:615071	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615071	Alazami syndrome		HP:0012471	PMID:22865833	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000739	OMIM:615071	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615071	Alazami syndrome		HP:0000007	PMID:22865833	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000322	PMID:22865833	PCS		9/9			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000369	PMID:22865833	PCS		6/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000325	PMID:22865833	PCS		9/9			P	HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000687	PMID:22865833	PCS		8/9			P	HPO:probinson[2023-01-21]
OMIM:615071	Alazami syndrome		HP:0000445	PMID:22865833	PCS		9/9			P	HPO:skoehler[2013-05-03];HPO:probinson[2023-01-21]
OMIM:142400	Hernia, hiatus		HP:0002036	OMIM:142400	IEA					P	HPO:iea[2009-02-17]
OMIM:142400	Hernia, hiatus		HP:0000006	OMIM:142400	IEA					I	HPO:iea[2009-02-17]
OMIM:142400	Hernia, hiatus		HP:0000765	OMIM:142400	IEA					P	HPO:iea[2009-02-17]
OMIM:609470	Left ventricular noncompaction 2		HP:0011664	PMID:15173023	PCS					P	HPO:probinson[2022-07-10]
OMIM:609470	Left ventricular noncompaction 2		HP:0000006	PMID:15173023	PCS					I	HPO:probinson[2022-07-10]
OMIM:600332	Rippling muscle disease 1		HP:0003760	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0003719	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0003738	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0003712	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0003559	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0000006	OMIM:600332	IEA					I	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0003457	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0003710	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:600332	Rippling muscle disease 1		HP:0008967	OMIM:600332	IEA					P	HPO:iea[2009-02-17]
OMIM:130900	Amelogenesis imperfecta, type III		HP:0000705	PMID:18252228	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-19]
OMIM:130900	Amelogenesis imperfecta, type III		HP:0009102	PMID:18252228	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2023-03-19]
OMIM:130900	Amelogenesis imperfecta, type III		HP:0000689	PMID:18252228	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-19]
OMIM:130900	Amelogenesis imperfecta, type III		HP:0000006	PMID:18252228	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-19]
OMIM:613428	Retinitis pigmentosa 54		HP:0007737	OMIM:613428	TAS					P	HPO:probinson[2013-06-02]
OMIM:613428	Retinitis pigmentosa 54		HP:0001099	PMID:20398884	PCS					P	HPO:probinson[2013-06-02]
OMIM:613428	Retinitis pigmentosa 54		HP:0000662	OMIM:613428	TAS					P	HPO:probinson[2013-06-02]
OMIM:613428	Retinitis pigmentosa 54		HP:0000007	PMID:20398886	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-20]
OMIM:613428	Retinitis pigmentosa 54		HP:0000505	PMID:20398884	PCS					P	HPO:probinson[2013-06-02]
OMIM:613428	Retinitis pigmentosa 54		HP:0000510	PMID:20398886	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-20]
OMIM:613428	Retinitis pigmentosa 54		HP:0007843	OMIM:613428	TAS					P	HPO:probinson[2013-06-02]
OMIM:613428	Retinitis pigmentosa 54		HP:0000512	OMIM:613428	TAS					P	HPO:probinson[2013-06-02]
OMIM:614347	Intellectual developmental disorder, autosomal recessive 28		HP:0000252	OMIM:614347	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614347	Intellectual developmental disorder, autosomal recessive 28		HP:0000750	OMIM:614347	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614347	Intellectual developmental disorder, autosomal recessive 28		HP:0000007	OMIM:614347	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614347	Intellectual developmental disorder, autosomal recessive 28		HP:0001270	OMIM:614347	TAS				HP:0012826	P	HPO:skoehler[2017-07-13]
OMIM:615059	Hypotrichosis 11		HP:0002289	PMID:9621144	PCS	HP:0003577	2/8			P	HPO:probinson[2022-03-20]
OMIM:615059	Hypotrichosis 11		HP:0002221	PMID:9621144	PCS					P	HPO:skoehler[2013-03-08];HPO:probinson[2022-03-20]
OMIM:615059	Hypotrichosis 11		HP:0100840	PMID:9621144	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-20]
OMIM:615059	Hypotrichosis 11		HP:0200102	PMID:9621144	PCS					P	HPO:skoehler[2013-06-05];HPO:probinson[2022-03-20]
OMIM:615059	Hypotrichosis 11		HP:0000006	PMID:9621144	PCS					I	HPO:skoehler[2013-03-08];HPO:probinson[2022-03-20]
OMIM:615059	Hypotrichosis 11		HP:0008070	PMID:9621144	PCS		8/8			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-20]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001276	PMID:15651030;OMIM:612736	PCS		11/15			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0008947	OMIM:612736	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0002069	PMID:15651030	PCS		1/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001250	PMID:15651030;OMIM:612736	PCS		11/15			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0002385	PMID:15651030	PCS		1/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001252	PMID:8651275	PCS	HP:0003593	2/2			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0002063	PMID:15651030	PCS		2/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001251	PMID:15651030;OMIM:612736	PCS		11/15			P	HPO:probinson[2022-08-15];HPO:skoehler[2010-06-19]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0003593	PMID:8651275	PCS		2/2			C	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0002061	PMID:15651030	PCS		1/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0000718	PMID:15651030	PCS		2/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0034321	PMID:15651030	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001249	OMIM:612736	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001347	OMIM:612736	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:6000484	PMID:9386672	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0000750	PMID:15651030;OMIM:612736	PCS		15/15			P	HPO:probinson[2012-07-16];HPO:probinson[2022-08-15];HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001344	PMID:15651030	PCS		2/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0002376	PMID:15651030	PCS		1/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0002373	PMID:15651030	PCS		1/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0010819	PMID:15651030	PCS		2/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0002572	PMID:15651030	PCS		1/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001263	OMIM:612736	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:6000722	PMID:15651030	PCS		4/4			P	HPO:probinson[2024-06-29]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0011344	PMID:8651275;PMID:15651030	PCS		7/7			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:6000748	PMID:20301745	PCS					P	HPO:probinson[2024-06-29]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0025051	PMID:7808840	PCS					P	HP:probinson[2019-01-27]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0012101	PMID:8651275	PCS		2/2			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0007153	OMIM:612736	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0000007	PMID:8651275	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001337	PMID:15651030	PCS		1/5			P	HPO:probinson[2022-08-15]
OMIM:612736	Cerebral creatine deficiency syndrome 2		HP:0001336	OMIM:612736	IEA					P	HPO:skoehler[2010-06-19]
OMIM:143050	Humeroradial synostosis		HP:0003041	OMIM:143050	IEA					P	HPO:iea[2009-02-17]
OMIM:143050	Humeroradial synostosis		HP:0000006	OMIM:143050	IEA					I	HPO:iea[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0003115	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0003134	OMIM:601992	PCS					P	HPO:probinson[2012-03-18]
OMIM:601992	Friedreich ataxia 2		HP:0005157	OMIM:601992	TAS					P	HPO:probinson[2014-02-15]
OMIM:601992	Friedreich ataxia 2		HP:0003232	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0003133	OMIM:601992	PCS					P	HPO:probinson[2012-03-18]
OMIM:601992	Friedreich ataxia 2		HP:0001691	OMIM:601992	TAS					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0001251	OMIM:601992	PCS					P	HPO:probinson[2012-03-18]
OMIM:601992	Friedreich ataxia 2		HP:0002062	OMIM:601992	PCS					P	HPO:probinson[2012-03-18]
OMIM:601992	Friedreich ataxia 2		HP:0000639	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0011441	OMIM:601992	PCS					P	HPO:probinson[2012-03-18]
OMIM:601992	Friedreich ataxia 2		HP:0003209	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0001626	OMIM:601992	TAS					P	HPO:skoehler[2014-03-24]
OMIM:601992	Friedreich ataxia 2		HP:0001765	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0002311	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0003621	OMIM:601992	PCS					C	HPO:probinson[2012-03-18]
OMIM:601992	Friedreich ataxia 2		HP:0002650	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0001761	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0003487	OMIM:601992	TAS					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0001260	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0002495	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0011397	OMIM:601992	PCS					P	HPO:probinson[2012-03-18]
OMIM:601992	Friedreich ataxia 2		HP:0000007	OMIM:601992	TAS					I	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0001635	OMIM:601992	TAS					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0001953	OMIM:601992	IEA					P	HPO:probinson[2009-02-17]
OMIM:601992	Friedreich ataxia 2		HP:0001315	OMIM:601992	PCS					P	HPO:probinson[2012-03-18]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0000252	PMID:38423010	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0006989	PMID:38423010	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0002015	PMID:38423010	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0003621	PMID:38423010	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0000750	PMID:38423010	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0002353	PMID:38423010	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0002079	PMID:38423010	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0001250	PMID:38423010	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0001272	PMID:38423010	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0002283	PMID:38423010	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0001274	PMID:38423010	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0001251	PMID:38423010	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0033454	PMID:38423010	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0000639	PMID:38423010	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0011342	PMID:38423010	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0000649	PMID:38423010	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0011463	PMID:38423010	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0008278	PMID:38423010	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0000648	PMID:38423010	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0000405	PMID:38423010	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0001249	PMID:38423010	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620784	Neurodevelopmental disorder plus optic atrophy		HP:0000006	PMID:38423010	PCS					I	ORCID:0000-0002-0736-9199[2024-07-29]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0002521	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0000494	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0010804	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0002540	PMID:31997314	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0000750	PMID:31997314;PMID:33381903	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0002650	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0031936	PMID:31997314;PMID:33381903	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0002373	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0001252	PMID:31997314;PMID:33381903	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0001263	PMID:31997314;PMID:33381903	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0003593	PMID:31997314	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0012704	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0033725	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0012469	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0032724	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0007270	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0000007	PMID:31997314	PCS					I	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0025336	PMID:31997314;PMID:33381903	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0000400	PMID:31997314;PMID:33381903	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:620790	Neurodevelopmental disorder with hypotonia and seizures		HP:0003623	PMID:33381903	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:619111	Coach syndrome 2		HP:0001320	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0003577	PMID:18950740	PCS		1/1			C	HPO:probinson[2022-06-11]
OMIM:619111	Coach syndrome 2		HP:0000486	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0001395	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0001274	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0001263	PMID:19574260	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0006580	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0004719	PMID:19574260	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0000657	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0000822	PMID:19574260	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0000007	PMID:18950740	PCS					I	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0005949	PMID:18950740	PCS	HP:0003593	1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0000238	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0002419	PMID:19574260	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0002612	PMID:19574260	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0002910	PMID:19574260	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0000589	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0000567	PMID:18950740	PCS	HP:0003577	1/1			P	HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0003259	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:619111	Coach syndrome 2		HP:0001249	PMID:18950740	PCS		1/1			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:616222	Temple syndrome		HP:0001773	OMIM:616222	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0000463	PMID:24891339	PCS		4/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0004322	OMIM:616222	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616222	Temple syndrome		HP:0001371	OMIM:616222	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0001252	PMID:24891339	PCS		38/41			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0001290	OMIM:616222	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616222	Temple syndrome		HP:0004482	OMIM:616222	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0001270	PMID:24891339	PCS		34/41			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0011220	PMID:24891339	PCS		17/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000238	OMIM:616222	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0030084	PMID:24891339	PCS		8/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000218	PMID:24891339	PCS		13/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0008734	OMIM:616222	TAS		HP:0040283			P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0003745	OMIM:616222	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616222	Temple syndrome		HP:0000358	OMIM:616222	TAS		HP:0040283			P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0001249	PMID:24891339	PCS		13/33			P	HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0001622	PMID:24891339	PCS		12/40			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000175	PMID:24891339	PCS		2/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000750	PMID:24891339	PCS		16/27			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0002155	OMIM:616222	TAS		HP:0040283			P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0002650	PMID:24891339	PCS		7/30			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0003124	PMID:24891339	PCS		5/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0011968	PMID:24891339	PCS		22/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0001382	PMID:24891339	PCS		12/19			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000193	PMID:24891339	PCS		2/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0005280	PMID:24891339	PCS		4/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000826	PMID:24891339	PCS		19/22			P	HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0001518	PMID:24891339	PCS		33/38			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0004904	PMID:24891339	PCS		3/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000403	PMID:24891339	PCS		9/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0025502	OMIM:616222	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616222	Temple syndrome		HP:0001956	OMIM:616222	TAS					P	HPO:skoehler[2015-03-22]
OMIM:616222	Temple syndrome		HP:0002007	PMID:24891339	PCS		17/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0001511	PMID:24891339	PCS		27/36			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0200055	PMID:24891339	PCS		34/39			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000322	PMID:24891339	PCS		9/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000006	PMID:24891339	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000028	PMID:24891339	PCS		3/23			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000347	PMID:24891339	PCS		12/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0001513	PMID:24891339	PCS		20/41			P	HPO:probinson[2023-02-10]
OMIM:616222	Temple syndrome		HP:0000445	PMID:24891339	PCS		6/51			P	HPO:skoehler[2015-03-22];HPO:probinson[2023-02-10]
OMIM:270350	SKUNK N-BUTYLMERCAPTAN, INABILITY TO SMELL		HP:0000007	OMIM:270350	IEA					I	HPO:iea[2009-02-17]
OMIM:270350	SKUNK N-BUTYLMERCAPTAN, INABILITY TO SMELL		HP:0000458	OMIM:270350	TAS					P	HPO:probinson[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0003301	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0002686	OMIM:187760	IEA					H	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0003016	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0002650	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0008839	OMIM:187760	IEA					P	HPO:skoehler[2010-06-20]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0006606	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0001591	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0003275	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0000888	OMIM:187760	TAS					P	HPO:probinson[2013-04-12]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0001602	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0001533	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0002866	OMIM:187760	IEA					P	HPO:iea[2009-02-17]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0000773	OMIM:187760	TAS					P	HPO:probinson[2013-04-12]
OMIM:187760	Thoracolaryngopelvic dysplasia		HP:0000006	OMIM:187760	IEA					I	HPO:iea[2009-02-17]
OMIM:614435	Hypoplastic left heart syndrome 2		HP:0003577	PMID:14607454	PCS		1/1			C	HPO:probinson[2023-01-23]
OMIM:614435	Hypoplastic left heart syndrome 2		HP:0001629	OMIM:614435	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614435	Hypoplastic left heart syndrome 2		HP:0011560	OMIM:614435	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614435	Hypoplastic left heart syndrome 2		HP:0004383	PMID:14607454	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:614435	Hypoplastic left heart syndrome 2		HP:0010883	OMIM:614435	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614435	Hypoplastic left heart syndrome 2		HP:0000006	PMID:14607454	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0001056	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000670	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0003555	PMID:8696340	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0003577	PMID:8696340	PCS		6/6			C	HPO:probinson[2022-05-14]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0004322	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000491	OMIM:226670	IEA					P	HPO:skoehler[2010-06-20]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0002164	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0004552	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0011859	OMIM:226670	TAS					P	HPO:skoehler[2012-10-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0003560	OMIM:226670	TAS					P	HPO:skoehler[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0033802	PMID:8696340	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0012227	OMIM:226670	TAS					P	HPO:probinson[2013-03-30]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0100298	PMID:8696340	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0001903	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0008066	PMID:8696340	PCS	HP:0003623	6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0009025	OMIM:226670	IEA					P	HPO:skoehler[2010-06-20]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0006297	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000007	PMID:8696340	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000972	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0008404	PMID:8696340	PCS	HP:0011463	6/6			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-04-30]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0002643	OMIM:226670	IEA					P	HPO:iea[2009-02-17]
OMIM:226670	Epidermolysis bullosa simplex with muscular dystrophy		HP:0003557	PMID:8696340	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:602531	Grange syndrome		HP:0004325	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0001156	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0005145	OMIM:602531	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0100546	OMIM:602531	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602531	Grange syndrome		HP:0001647	OMIM:602531	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0100817	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0000007	PMID:27939641	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-08]
OMIM:602531	Grange syndrome		HP:0002757	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0002659	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0001159	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0040019	OMIM:602531	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602531	Grange syndrome		HP:0001920	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602531	Grange syndrome		HP:0001249	OMIM:602531	TAS					P	HPO:skoehler[2017-07-13]
OMIM:155140	Meckel diverticulum		HP:0002245	OMIM:155140	IEA					P	HPO:iea[2009-02-17]
OMIM:155140	Meckel diverticulum		HP:0000006	OMIM:155140	IEA					I	HPO:iea[2009-02-17]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003236	OMIM:617882	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0000365	PMID:14733962	PCS		1/6			P	HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003596	PMID:14733962	PCS		1/4			C	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003376	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001251	OMIM:617882	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0002460	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001270	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001171	OMIM:617882	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003391	OMIM:617882	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0000639	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0007141	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0011463	PMID:14733962	PCS		1/6			C	HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0007340	PMID:14733962	PCS		2/6			P	HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0011462	PMID:14733962	PCS		2/4			C	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0002936	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0002515	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003701	OMIM:617882	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001265	PMID:14733962	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003621	PMID:14733962	PCS		1/4			C	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003487	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001288	PMID:14733962	PCS		2/12			P	HPO:probinson[2023-04-08];HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001761	PMID:14733962	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001284	OMIM:617882	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0000407	OMIM:617882	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0007210	PMID:14733962	PCS		1/6			P	HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0009830	PMID:14733962	PCS		1/6			P	HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0002527	PMID:14733962	PCS		1/6			P	HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0001257	OMIM:617882	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0000006	PMID:14733962	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:617882	Charcot-Marie-Tooth disease, dominant intermediate G		HP:0003677	OMIM:617882	IEA					C	HPO:skoehler[2018-10-08]
OMIM:616544	Retinitis pigmentosa 73		HP:0001133	PMID:25859010	PCS					P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0007737	PMID:25859010	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0030501	PMID:25859010	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0003596	PMID:25859010	PCS		3/6			C	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0000662	PMID:25859010	PCS		5/6			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0030786	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0000551	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0001123	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0031609	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0030529	PMID:25859010	PCS		4/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0100014	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0025708	PMID:25859010	PCS		1/6			C	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0500087	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0011463	PMID:25859010	PCS		2/6			C	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0000007	PMID:25859010	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0007663	PMID:25859010	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0000603	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0000543	PMID:25859010	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0000510	PMID:25859010	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0000622	PMID:25859010	PCS		1/6			P	HPO:probinson[2023-02-10]
OMIM:616544	Retinitis pigmentosa 73		HP:0001105	PMID:25859010	PCS		6/6			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-10]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000286	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000384	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0006989	PMID:31363758	PCS		1/6			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0001250	PMID:31363758	PCS		3/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0001171	PMID:31363758	PCS		2/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0010047	PMID:31363758	PCS		2/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000280	PMID:31363758	PCS		3/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0001270	PMID:31363758	PCS		6/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0008093	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0011359	PMID:31363758	PCS		2/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0011220	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0008954	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0001249	PMID:31363758	PCS		8/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0005768	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000252	PMID:31363758	PCS					P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000431	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0005643	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000750	PMID:31363758	PCS		8/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0002133	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0002079	PMID:31363758	IEA		2/6			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000294	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0011369	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0001182	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0011623	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0010041	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0012168	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0010044	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000729	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000007	PMID:31363758	PCS					I	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0000821	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0001335	PMID:31363758	PCS		3/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0001257	PMID:31363758	PCS		7/8			P	HPO:probinson[2020-06-14]
OMIM:618569	Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly		HP:0009778	PMID:31363758	PCS		1/8			P	HPO:probinson[2020-06-14]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0002454	PMID:27431290	PCS		2/2			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0003577	PMID:30059600	PCS		5/5			C	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0000750	PMID:27431290;PMID:30059600	PCS		7/7			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0000431	PMID:30059600	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0031936	PMID:27431290	PCS		2/2			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0002033	PMID:27431290;PMID:30059600	PCS		7/7			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0001252	PMID:27431290	PCS	HP:0003623	2/2			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0001252	PMID:30059600	PCS		5/5			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0001263	PMID:27431290;PMID:30059600	PCS		7/7			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0000294	PMID:30059600	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0001270	PMID:30059600	PCS		5/5			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0033725	PMID:30059600	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0001518	PMID:30059600	PCS	HP:0003577	5/5			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0000007	PMID:27431290	PCS					I	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0002317	PMID:27431290	PCS		2/2			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0002359	PMID:27431290	PCS		2/2			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0000664	PMID:30059600	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0000278	PMID:30059600	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:619844	Intellectual developmental disorder with or without peripheral neuropathy		HP:0003623	PMID:27431290	PCS		2/2			C	HPO:probinson[2022-05-31]
OMIM:241600	Immunodeficiency 43		HP:0003621	PMID:25702838	PCS		1/2			C	HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0025044	PMID:25702838	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0410299	PMID:25702838	PCS		2/2			P	HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0003022	OMIM:241600	IEA					P	HPO:iea[2009-02-17]
OMIM:241600	Immunodeficiency 43		HP:0410243	PMID:25702838	PCS		0/2			P	HPO:probinson[2022-11-20];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0002110	PMID:25702838	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0410240	PMID:25702838	PCS		0/2			P	HPO:probinson[2022-11-20];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0003075	PMID:25702838	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0001482	PMID:25702838	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0003073	PMID:16549777;PMID:25702838	PCS		4/4			P	HPO:probinson[2013-03-10];HPO:probinson[2022-11-20];HPO:probinson[2022-11-20];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0010976	PMID:25702838	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0025708	PMID:25702838	PCS		1/2			C	HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0033670	PMID:25702838	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0000007	PMID:16549777	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0025347	PMID:16549777;PMID:25702838	PCS		4/4			P	HPO:probinson[2022-11-20];HPO:probinson[2022-11-20];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0002986	OMIM:241600	TAS					P	HPO:probinson[2013-03-10]
OMIM:241600	Immunodeficiency 43		HP:0002205	PMID:25702838	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0004315	PMID:16549777;PMID:25702838	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-20];HPO:probinson[2022-11-20];HPO:probinson[2022-11-20]
OMIM:241600	Immunodeficiency 43		HP:0040218	PMID:25702838	PCS		1/2			P	HPO:probinson[2022-11-20]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0001397	OMIM:615918	TAS					P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0008936	PMID:24827421	PCS	HP:0003623	2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0002059	PMID:33153448	PCS		1/1			P	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0003577	PMID:24827421	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0002079	PMID:24827421	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0001250	PMID:33153448	PCS		1/1			P	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0001263	PMID:33153448	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0002151	PMID:24827421	PCS	HP:0003623	2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0002151	PMID:33153448	PCS		1/1			P	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0003593	PMID:33153448	IEA		1/1			C	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0011813	PMID:24827421	IEA		1/1			P	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0000817	PMID:33153448	PCS		1/1			P	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0002509	PMID:24827421	PCS	HP:0003623	2/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0002509	PMID:33153448	PCS		1/1			P	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0000007	PMID:24827421	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0008358	PMID:33153448	PCS		1/1			P	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0003811	PMID:24827421	PCS		2/2			C	HPO:probinson[2022-03-30]
OMIM:615918	Combined oxidative phosphorylation deficiency 21		HP:0003348	PMID:33153448	PCS		1/1			P	HPO:probinson[2022-03-30]
OMIM:176000	Porphyria, acute intermittent		HP:0002014	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0003401	OMIM:176000	TAS					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0003489	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0002013	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0001250	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0000020	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0003163	OMIM:176000	TAS					P	HPO:probinson[2012-04-11]
OMIM:176000	Porphyria, acute intermittent		HP:0002590	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0003470	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0000716	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:4000199	OMIM:176000	TAS					P	HPO:probinson[2024-01-06]
OMIM:176000	Porphyria, acute intermittent		HP:0000739	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0000822	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0000725	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0001649	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0100518	OMIM:176000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176000	Porphyria, acute intermittent		HP:0002018	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0001324	OMIM:176000	TAS					P	HPO:probinson[2012-04-11]
OMIM:176000	Porphyria, acute intermittent		HP:0002019	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0000006	OMIM:176000	IEA					I	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0002027	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0002203	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0000016	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:176000	Porphyria, acute intermittent		HP:0001402	OMIM:176000	IEA					P	HPO:probinson[2009-02-17]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0002014	OMIM:601979	IEA					P	HPO:iea[2009-02-17]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0000939	OMIM:601979	IEA					P	HPO:iea[2009-02-17]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0002240	OMIM:601979	IEA					P	HPO:iea[2009-02-17]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0011424	OMIM:601979	IEA					P	HPO:iea[2009-02-17]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0000988	OMIM:601979	IEA					P	HPO:iea[2009-02-17]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0000006	OMIM:601979	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0002633	OMIM:601979	IEA					P	HPO:iea[2009-02-17]
OMIM:601979	Hyperzincemia with functional zinc depletion		HP:0002721	OMIM:601979	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0001771	OMIM:604801	TAS					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0003236	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0003720	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0010628	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0003560	OMIM:604801	TAS					P	HPO:probinson[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0001290	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0001270	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0003391	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0012037	OMIM:604801	TAS					P	HPO:probinson[2012-07-27]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0012036	OMIM:604801	TAS					P	HPO:probinson[2012-07-27]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0009113	PMID:10677302	PCS	HP:0011463				P	HPO:probinson[2014-05-29]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0000007	OMIM:604801	IEA					I	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0002878	PMID:10677302	PCS	HP:0011463				P	HPO:probinson[2014-05-29]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0003547	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:604801	Muscular dystrophy, congenital, 1B		HP:0003306	OMIM:604801	IEA					P	HPO:iea[2009-02-17]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0003577	PMID:28017832	PCS		1/3			C	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0001762	PMID:28017832	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0008064	PMID:28017832	PCS		3/3			P	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0007460	PMID:28017832	PCS		1/3			P	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0000407	PMID:28017832	PCS		3/3			P	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0001263	PMID:28017832	PCS		2/3			P	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0003593	PMID:28017832	PCS		2/3			C	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0000007	PMID:28017832	PCS					I	HPO:probinson[2022-08-27]
OMIM:620009	Keratoderma-ichthyosis-deafness syndrome, autosomal recessive		HP:0007545	PMID:28017832	PCS		3/3			P	HPO:probinson[2022-08-27]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0000252	PMID:29330545	PCS		1/2			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0007270	PMID:29330545	PCS	HP:0003593	1/2			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0011150	PMID:29330545	PCS	HP:0011463	1/2			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0004322	PMID:29330545	PCS		1/2			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0001263	PMID:29330545	PCS		2/2			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0007166	PMID:29330545	PCS		0/2			P	HPO:probinson[2020-07-11];HPO:probinson[2024-03-16]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0032794	PMID:29330545	PCS		1/2			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0010841	PMID:29330545	PCS		1/2			P	HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0000006	PMID:29330545	PCS					I	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618596	Epilepsy, idiopathic generalized, susceptibility to, 16		HP:0002500	PMID:29330545	PCS		1/2			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0001892	PMID:22492991	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0002521	PMID:23934111;PMID:24781210	PCS		3/3			P	HPO:probinson[2022-05-30];HPO:skoehler[2018-10-08];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0002188	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000463	OMIM:300884	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0001371	PMID:23033978	PCS		1/1			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0001250	PMID:22492991;PMID:23033978	PCS		2/2			P	HPO:probinson[2022-05-30];HPO:skoehler[2013-06-06];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0001252	PMID:23033978	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0002240	PMID:22492991	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0003593	PMID:22492991;PMID:23934111;PMID:24781210	PCS		4/4			C	HPO:skoehler[2013-11-18];HPO:probinson[2022-05-30];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0032794	PMID:23934111	PCS		1/2			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000280	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0012469	PMID:23934111;PMID:24781210	PCS		3/3			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0002719	PMID:22492991	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000817	OMIM:300884	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000316	PMID:23033978	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000238	PMID:23033978	PCS		1/1			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000256	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0003645	PMID:22492991	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0003642	PMID:22492991	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0002059	PMID:24781210	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000252	PMID:22492991	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0002650	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0011968	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0010819	PMID:23934111	PCS		1/2			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0001263	PMID:23934111;PMID:24781210;PMID:23033978	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-05-30];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0002071	PMID:22492991	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000308	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0032792	PMID:23934111	PCS		1/2			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0007256	PMID:22492991	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000648	PMID:22492991	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0001417	PMID:23934111	PCS					I	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0200055	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000666	PMID:22492991	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000369	PMID:23033978	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-30]
OMIM:300884	Epileptic encephalopathy, early infantile, 36		HP:0000742	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0003477	PMID:33964137	PCS		4/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001250	PMID:33964137	PCS		1/9			P	HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001260	PMID:33964137	PCS		9/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001251	PMID:33964137	PCS		9/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001270	PMID:33964137	PCS		5/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0033725	PMID:33964137	PCS		9/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0011463	PMID:33964137	PCS		4/4			C	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0000407	PMID:33964137	PCS	HP:0003621	9/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0000007	PMID:33964137	PCS					I	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0003429	PMID:33964137	PCS		9/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001258	PMID:33964137	PCS		9/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0002910	PMID:33964137	PCS		8/8			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001249	PMID:33964137	PCS		5/9			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001347	PMID:33964137	PCS		8/8			P	HPO:probinson[2022-03-21]
OMIM:619688	Leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy		HP:0001644	PMID:33964137	PCS	HP:0003621	9/9			P	HPO:probinson[2022-03-21]
OMIM:605289	Split-Hand/foot malformation 4		HP:0010173	PMID:10839977	PCS					P	HPO:probinson[2013-03-24]
OMIM:605289	Split-Hand/foot malformation 4		HP:0001199	OMIM:605289	TAS					P	HPO:skoehler[2015-08-16]
OMIM:605289	Split-Hand/foot malformation 4		HP:0100257	OMIM:605289	TAS					P	HPO:probinson[2013-03-24]
OMIM:605289	Split-Hand/foot malformation 4		HP:0001839	OMIM:605289	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605289	Split-Hand/foot malformation 4		HP:0001171	OMIM:605289	IEA					P	HPO:skoehler[2015-01-27]
OMIM:605289	Split-Hand/foot malformation 4		HP:0005914	PMID:10839977	PCS					P	HPO:probinson[2013-03-24]
OMIM:605289	Split-Hand/foot malformation 4		HP:0001159	OMIM:605289	TAS					P	HPO:probinson[2013-01-09]
OMIM:605289	Split-Hand/foot malformation 4		HP:0009767	PMID:10839977	PCS					P	HPO:probinson[2013-03-24]
OMIM:605289	Split-Hand/foot malformation 4		HP:0000006	PMID:10839977	PCS					I	HPO:probinson[2013-03-24]
OMIM:605289	Split-Hand/foot malformation 4		HP:0001964	PMID:10839977	PCS					P	HPO:probinson[2013-03-24]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000175	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000483	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0010529	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0002650	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0001250	PMID:35227461	PCS		2/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000194	PMID:35227461	PCS		3/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0001263	PMID:35227461	PCS		4/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000272	PMID:35227461	PCS		3/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0003593	PMID:35227461	PCS					C	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0100023	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000729	PMID:35227461	PCS		4/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000316	PMID:35227461	PCS		4/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000646	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0001845	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000007	PMID:35227461	PCS					I	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000722	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000218	PMID:35227461	PCS		3/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0007018	PMID:35227461	PCS		2/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0001488	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0001249	PMID:35227461	PCS		4/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000545	PMID:35227461	PCS		2/4			P	HPO:probinson[2022-09-04]
OMIM:620021	Intellectual developmental disorder with autism and dysmorphic facies		HP:0000369	PMID:35227461	PCS		1/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:619878	Spermatogenic failure 73		HP:0003251	PMID:35476666	PCS		2/2			P	HPO:probinson[2022-07-11]
OMIM:619878	Spermatogenic failure 73		HP:0011462	PMID:35476666	PCS		2/2			C	HPO:probinson[2022-07-11]
OMIM:619878	Spermatogenic failure 73		HP:0000007	PMID:35476666	PCS					I	HPO:probinson[2022-07-11]
OMIM:619878	Spermatogenic failure 73		HP:0031038	PMID:35476666	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:619878	Spermatogenic failure 73		HP:0011961	PMID:35476666	PCS		2/2			P	HPO:probinson[2022-07-11]
OMIM:100800	Achondroplasia		HP:0003015	PMID:16411219	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0008947	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0005733	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0003577	PMID:16411219	PCS		1/1			C	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0002980	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0001377	OMIM:100800	TAS					P	HPO:probinson[2012-04-17]
OMIM:100800	Achondroplasia		HP:0001355	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0002089	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0008905	PMID:16411219	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0004565	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0001156	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0002761	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0005257	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0003375	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0002781	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0003097	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0003031	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0003093	OMIM:100800	TAS					P	HPO:probinson[2012-04-17]
OMIM:100800	Achondroplasia		HP:0001270	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0004060	PMID:16411219	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0100864	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0008450	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0002938	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0002979	PMID:16411219	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0000238	PMID:16411219	PCS		1/1			P	HPO:probinson[2012-04-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0001522	PMID:16411219	PCS		1/1			C	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0008414	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0000256	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0000773	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0001788	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0002512	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0002677	PMID:16411219	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0001561	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0000452	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0002970	OMIM:100800	TAS					P	HPO:probinson[2012-04-17]
OMIM:100800	Achondroplasia		HP:0011968	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0002098	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0000272	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:6000920	PMID:33103849	PCS					P	HPO:probinson[2024-08-03]
OMIM:100800	Achondroplasia		HP:0011800	OMIM:100800	TAS					P	HPO:skoehler[2013-11-28]
OMIM:100800	Achondroplasia		HP:0005280	PMID:16411219	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0000403	OMIM:100800	TAS					P	HPO:probinson[2012-04-17]
OMIM:100800	Achondroplasia		HP:0000405	OMIM:100800	IEA					P	HPO:iea[2009-02-17]
OMIM:100800	Achondroplasia		HP:0002007	PMID:16411219	PCS		1/1			P	HPO:probinson[2012-04-17];HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0008921	OMIM:100800	TAS					P	HPO:probinson[2012-04-17]
OMIM:100800	Achondroplasia		HP:0002986	PMID:16411219	PCS		1/1			P	HPO:probinson[2022-11-10]
OMIM:100800	Achondroplasia		HP:0000006	PMID:16411219	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0002322	PMID:27134041;PMID:30398675;PMID:27753167	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0002067	PMID:27134041;PMID:30398675	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0031825	PMID:27134041	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001250	PMID:27134041;PMID:30398675;PMID:27753167	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0002362	PMID:27753167	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0003390	PMID:27134041;PMID:27753167	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0100786	PMID:27134041;PMID:30398675;PMID:27753167	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0000716	PMID:27134041;PMID:27753167	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0011463	PMID:27134041;PMID:27753167	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0032121	PMID:27753167	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0000739	PMID:27134041;PMID:27753167	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0000514	PMID:27134041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0009027	PMID:27134041	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0000711	PMID:27134041;PMID:27753167	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0000736	PMID:27134041	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001249	PMID:27134041;PMID:27753167	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001347	PMID:27134041;PMID:30398675;PMID:27753167	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0003763	PMID:27134041;PMID:30398675;PMID:27753167	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0002015	PMID:27134041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001300	PMID:27134041;PMID:30398675;PMID:27753167	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001288	PMID:27134041;PMID:30398675;PMID:27753167	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0000298	PMID:30398675;PMID:27753167	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0003487	PMID:27134041;PMID:30398675;PMID:27753167	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:5200321	PMID:27134041;PMID:27753167	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0002396	PMID:30398675;PMID:27753167	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001260	PMID:27134041;PMID:27753167	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001263	PMID:27134041;PMID:30398675	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0002174	PMID:27134041;PMID:30398675;PMID:27753167	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0002172	PMID:27134041;PMID:27753167	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0000007	PMID:27134041	PCS					I	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0001257	PMID:27753167	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:620747	Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities		HP:0008944	PMID:27134041;PMID:27753167	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-21]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001298	OMIM:615924	TAS				HP:0003676	P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0002059	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0003676	OMIM:615924	TAS					C	HPO:skoehler[2015-12-30]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0002155	OMIM:615924	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0000750	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001332	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0002376	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001250	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0002371	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0002240	OMIM:615924	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001251	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0002273	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0002529	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0007256	OMIM:615924	TAS					P	HPO:skoehler[2015-01-04]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0000007	OMIM:615924	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0000752	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001268	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001257	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001337	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001347	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615924	Encephalopathy, progressive, with or without lipodystrophy		HP:0001336	OMIM:615924	TAS					P	HPO:skoehler[2014-08-24]
OMIM:613399	Familial breast-ovarian cancer-1		HP:0003002	PMID:20400964	PCS	HP:0003596		FEMALE		P	HPO:probinson[2017-11-11]
OMIM:613399	Familial breast-ovarian cancer-1		HP:0025318	PMID:22538716	PCS	HP:0003596		FEMALE		P	HPO:probinson[2017-11-11]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0006009	OMIM:300106	TAS					P	HPO:probinson[2012-06-03]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001377	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001773	OMIM:300106	TAS					P	HPO:probinson[2012-05-27]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001156	PMID:27236923	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003311	OMIM:300106	IEA				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003275	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0004981	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001230	OMIM:300106	TAS					P	HPO:probinson[2012-06-03]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0004000	OMIM:300106	TAS					P	HPO:probinson[2018-04-13]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0010049	OMIM:300106	TAS					P	HPO:probinson[2012-06-03]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0006371	OMIM:300106	TAS					P	HPO:skoehler[2013-04-13]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0011463	PMID:27236923	PCS		9/9			C	HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0010230	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0002938	PMID:27236923	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0009486	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0002515	PMID:27236923	PCS		9/9			P	HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0006059	OMIM:300106	TAS					P	HPO:probinson[2012-05-27]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003988	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0000894	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001249	PMID:27236923	PCS		0/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-16]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0009803	OMIM:300106	TAS					P	HPO:probinson[2012-06-03]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003521	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003026	OMIM:300106	TAS					P	HPO:probinson[2012-05-27]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0005622	OMIM:300106	TAS					P	HPO:probinson[2012-05-27]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0004379	PMID:27236923	PCS		0/17			P	HPO:probinson[2023-02-22];HPO:probinson[2024-03-16]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0004279	OMIM:300106	TAS					P	HPO:probinson[2012-05-27]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0002673	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003025	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0002651	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0002970	PMID:27236923	PCS		9/9			P	HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001382	PMID:27236923	PCS		5/9			P	HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0004573	OMIM:300106	TAS					P	HPO:probinson[2012-06-10]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0005066	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003085	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0003180	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0011940	OMIM:300106	TAS					P	HPO:probinson[2012-06-10]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0002808	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001419	PMID:27236923	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0000926	PMID:27236923	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0002869	OMIM:300106	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0000327	OMIM:300106	IEA				HP:0012825	P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001999	PMID:27236923	PCS		0/9			P	HPO:probinson[2024-03-09]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0000768	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0000922	OMIM:300106	IEA					P	HPO:iea[2009-02-17]
OMIM:300106	Spondyloepimetaphyseal dysplasia, X-linked		HP:0001216	OMIM:300106	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000582	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0009914	OMIM:264480	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001674	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0002023	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000089	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001651	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000161	OMIM:264480	TAS					P	HPO:probinson[2024-03-29]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001252	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001274	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0002086	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001290	OMIM:264480	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0002084	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001629	OMIM:264480	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0011662	OMIM:264480	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0002937	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000238	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000813	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000835	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000878	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000358	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000054	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000252	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001321	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001162	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001360	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001680	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0004691	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0009099	OMIM:264480	TAS					P	HPO:probinson[2024-03-29]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000568	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000601	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000007	OMIM:264480	IEA					I	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001539	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001830	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0001631	OMIM:264480	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0002126	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000369	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000028	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000204	OMIM:264480	IEA		HP:0040282			P	HPO:skoehler[2010-06-20]
OMIM:264480	Pseudotrisomy 13 syndrome		HP:0000104	OMIM:264480	IEA					P	HPO:iea[2009-02-17]
OMIM:614390	Pregnancy loss, recurrent, susceptibility to, 2		HP:0011462	PMID:11506076	PCS					C	HPO:probinson[2023-02-11]
OMIM:614390	Pregnancy loss, recurrent, susceptibility to, 2		HP:0200067	PMID:11506076	PCS					H	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-11]
OMIM:614390	Pregnancy loss, recurrent, susceptibility to, 2		HP:0000006	PMID:11506076	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:211180	Bowen-Conradi syndrome		HP:0000252	OMIM:211180	IEA					P	HPO:iea[2009-02-17]
OMIM:211180	Bowen-Conradi syndrome		HP:0001838	OMIM:211180	IEA					P	HPO:iea[2009-02-17]
OMIM:211180	Bowen-Conradi syndrome		HP:0001518	OMIM:211180	IEA					P	HPO:iea[2009-02-17]
OMIM:211180	Bowen-Conradi syndrome		HP:0000448	OMIM:211180	IEA					P	HPO:iea[2009-02-17]
OMIM:211180	Bowen-Conradi syndrome		HP:0000007	OMIM:211180	IEA					I	HPO:iea[2009-02-17]
OMIM:211180	Bowen-Conradi syndrome		HP:0004209	OMIM:211180	IEA					P	HPO:iea[2009-02-17]
OMIM:211180	Bowen-Conradi syndrome		HP:0001367	OMIM:211180	IEA					P	HPO:iea[2009-02-17]
OMIM:211180	Bowen-Conradi syndrome		HP:0000347	OMIM:211180	IEA					P	HPO:iea[2009-02-17]
OMIM:610069	Polyposis syndrome, hereditary mixed, 2		HP:0005227	PMID:16525031	PCS					P	HPO:skoehler[2013-02-23]
OMIM:610069	Polyposis syndrome, hereditary mixed, 2		HP:0012198	PMID:16525031	PCS					P	HPO:probinson[2013-03-11]
OMIM:610069	Polyposis syndrome, hereditary mixed, 2		HP:0003003	PMID:16525031	PCS					P	HPO:skoehler[2013-02-23]
OMIM:610069	Polyposis syndrome, hereditary mixed, 2		HP:0012183	PMID:16525031	PCS					P	HPO:probinson[2013-03-11]
OMIM:610069	Polyposis syndrome, hereditary mixed, 2		HP:0000006	PMID:16525031	PCS					I	HPO:skoehler[2013-01-09]
OMIM:617706	Spermatogenic failure 22		HP:0030974	PMID:28206990	PCS		1/4			P	HPO:probinson[2022-09-12];HPO:probinson[2022-09-12]
OMIM:617706	Spermatogenic failure 22		HP:0003251	PMID:28206990	PCS		4/4			P	HPO:probinson[2022-09-12];HPO:probinson[2022-09-12]
OMIM:617706	Spermatogenic failure 22		HP:0011462	PMID:28206990	PCS		4/4			C	HPO:probinson[2022-09-12]
OMIM:617706	Spermatogenic failure 22		HP:0000007	PMID:28206990	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-12]
OMIM:617706	Spermatogenic failure 22		HP:0011961	PMID:28206990	PCS		3/4			P	HPO:probinson[2022-09-12]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0003049	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0003577	PMID:19142688	PCS		1/1			C	HPO:probinson[2023-02-28]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001762	PMID:19142688	PCS	HP:0003577	1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001156	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001772	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0000160	OMIM:618435	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001182	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001181	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0010557	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0012385	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0010055	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0002827	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0030084	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001852	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001840	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0000325	OMIM:618435	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0000006	PMID:12865991	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-28]
OMIM:618435	Arthrogryposis, distal, type 2B2		HP:0001831	OMIM:618435	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0000252	PMID:24699222	PCS		2/6			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0001344	PMID:24699222	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0000750	PMID:24699222	PCS		6/6			P	HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0001250	PMID:24699222	PCS		5/6			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0001263	PMID:24699222	PCS		6/6			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0003593	PMID:24699222	PCS		2/6			C	HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0025708	PMID:24699222	PCS		1/6			C	HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0002917	PMID:24699222	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0011463	PMID:24699222	PCS		1/6			C	HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0100954	PMID:24699222	PCS		1/6			P	HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0000007	PMID:24699222	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0025501	PMID:24699222	PCS		2/5			P	HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0001249	PMID:24699222	PCS		6/6			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-02-04]
OMIM:616418	Hypomagnesemia, seizures, and impaired intellectual development 1		HP:0000006	PMID:24699222	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:611377	Brachydactyly, type B2		HP:0006109	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:611377	Brachydactyly, type B2		HP:0000540	OMIM:611377;PMID:17668388	PCS		HP:0040283			P	HPO:iea[2010-02-15]
OMIM:611377	Brachydactyly, type B2		HP:0010621	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:611377	Brachydactyly, type B2		HP:0010554	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0010194	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2010-02-15]
OMIM:611377	Brachydactyly, type B2		HP:0010034	OMIM:611377;PMID:17668388	PCS		7/10			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0006152	OMIM:611377;PMID:17668388	PCS		16/16			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0000407	OMIM:611377;PMID:17668388	PCS		HP:0040283			P	HPO:iea[2010-02-15]
OMIM:611377	Brachydactyly, type B2		HP:0008386	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0010185	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0009882	OMIM:611377	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611377	Brachydactyly, type B2		HP:0009843	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0009623	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0008368	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0009702	OMIM:611377;PMID:17668388	PCS		10/10			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0000006	OMIM:611377;PMID:17668388	PCS					I	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0009835	OMIM:611377;PMID:17668388	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:611377	Brachydactyly, type B2		HP:0001204	OMIM:611377;PMID:17668388	PCS		5/5			P	HPO:iea[2010-02-15]
OMIM:620814	MHC class I deficiency 3		HP:0000099	PMID:12149238	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620814	MHC class I deficiency 3		HP:0003596	PMID:12149238	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620814	MHC class I deficiency 3		HP:0032275	PMID:12149238	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620814	MHC class I deficiency 3		HP:0000007	PMID:12149238	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620814	MHC class I deficiency 3		HP:0002205	PMID:12149238	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:235750	Hirschsprung disease with ulnar polydactyly, polysyndactyly of bigtoes, and ventricular septal defect		HP:0005873	OMIM:235750	IEA					P	HPO:iea[2009-02-17]
OMIM:235750	Hirschsprung disease with ulnar polydactyly, polysyndactyly of bigtoes, and ventricular septal defect		HP:0001629	OMIM:235750	IEA					P	HPO:iea[2009-02-17]
OMIM:235750	Hirschsprung disease with ulnar polydactyly, polysyndactyly of bigtoes, and ventricular septal defect		HP:0002251	OMIM:235750	IEA					P	HPO:iea[2009-02-17]
OMIM:235750	Hirschsprung disease with ulnar polydactyly, polysyndactyly of bigtoes, and ventricular septal defect		HP:0000007	OMIM:235750	IEA					I	HPO:iea[2009-02-17]
OMIM:235750	Hirschsprung disease with ulnar polydactyly, polysyndactyly of bigtoes, and ventricular septal defect		HP:0001841	OMIM:235750	TAS					P	HPO:probinson[2012-07-24]
OMIM:618353	Oocyte maturation defect 6		HP:0008222	PMID:29895852	PCS					P	HPO:probinson[2019-06-13]
OMIM:618353	Oocyte maturation defect 6		HP:0000007	PMID:29895852	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:618353	Oocyte maturation defect 6		HP:0020157	PMID:29895852	PCS					P	HPO:probinson[2019-09-07];HPO:probinson[2019-09-07]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0000486	PMID:19056803	PCS		2/3			P	HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0001310	PMID:19056803	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0001250	PMID:19056803	PCS		1/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0000020	PMID:19056803	PCS		1/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0001251	PMID:19056803	PCS		3/3			P	HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0002064	PMID:19056803	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0002061	PMID:19056803	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0002080	PMID:19056803	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0100543	PMID:19056803	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0000639	PMID:19056803	PCS		0/3			P	HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0011463	PMID:19056803	PCS		1/3			C	HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0000514	PMID:19056803	PCS		2/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0002936	PMID:19056803	PCS		1/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0003429	PMID:19056803	PCS		3/3			P	HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0002019	PMID:19056803	PCS		1/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0001347	PMID:19056803	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0003621	PMID:19056803	PCS		2/3			C	HPO:probinson[2023-05-08];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0002650	PMID:19056803	PCS		1/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0003487	PMID:19056803	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0002079	PMID:19056803	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0001761	PMID:19056803	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0001260	PMID:19056803	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0000407	PMID:19056803	PCS		1/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0000007	PMID:19056803	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0001258	PMID:19056803	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-05-08]
OMIM:613206	Spastic paraplegia 44, autosomal recessive		HP:0006986	PMID:19056803	PCS		3/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-05-08]
OMIM:190340	Trichodiscomas, familial multiple		HP:0001595	OMIM:190340	IEA					P	HPO:iea[2009-02-17]
OMIM:190340	Trichodiscomas, familial multiple		HP:0000006	OMIM:190340	IEA					I	HPO:iea[2009-02-17]
OMIM:614569	Multiple enchondromatosis, Maffucci type		HP:0006765	PMID:8408836	PCS		30%			P	HPO:probinson[2017-06-24]
OMIM:614569	Multiple enchondromatosis, Maffucci type		HP:0002756	PMID:8408836	PCS					P	HPO:probinson[2017-06-24]
OMIM:614569	Multiple enchondromatosis, Maffucci type		HP:0005701	PMID:8408836	PCS					P	HPO:probinson[2017-06-24]
OMIM:614569	Multiple enchondromatosis, Maffucci type		HP:0001028	PMID:8408836	PCS					P	HPO:probinson[2017-06-24]
OMIM:615663	Warburg micro syndrome 4		HP:0003577	PMID:24239381	PCS		7/7			C	HPO:probinson[2022-03-26]
OMIM:615663	Warburg micro syndrome 4		HP:0000046	PMID:24239381	PCS		1/2			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0003431	PMID:24239381	PCS		2/2			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0002540	PMID:24239381	PCS		7/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000343	PMID:24239381	PCS		1/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0004322	PMID:24239381	PCS		5/5			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000463	PMID:24239381	PCS		1/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0001272	PMID:24239381	PCS		3/7			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0002120	PMID:24239381	PCS		4/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0001371	PMID:24239381	PCS		2/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0001250	PMID:24239381	PCS		2/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0003199	PMID:24239381	PCS					P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000160	PMID:24239381	PCS					P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000482	PMID:24239381	PCS		3/4			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0001290	PMID:24239381	PCS		4/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0012650	PMID:24239381	PCS		4/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000519	PMID:24239381	PCS	HP:0003577	7/7		HP:0012832	P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0008850	PMID:24239381	PCS		7/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0008872	PMID:24239381	PCS		4/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0008734	PMID:24239381	PCS		1/2			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0001007	PMID:24239381	PCS		1/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000054	PMID:24239381	PCS		2/2			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0002510	OMIM:615663	TAS					P	HPO:skoehler[2014-04-04]
OMIM:615663	Warburg micro syndrome 4		HP:0001344	PMID:24239381	PCS		4/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000750	PMID:24239381	PCS		7/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0002133	PMID:24239381	PCS		1/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0002079	PMID:24239381	PCS		4/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0003487	PMID:24239381	PCS		2/7			P	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000490	PMID:24239381	PCS		4/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000294	PMID:24239381	PCS		1/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0005484	PMID:24239381	PCS		7/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000508	PMID:24239381	PCS		2/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000426	PMID:24239381	PCS		2/7			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000007	PMID:24239381	PCS					I	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000568	PMID:24239381	PCS		3/4			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000648	PMID:24239381	PCS				HP:0003676	P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000505	PMID:24239381	PCS		5/5			P	HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000248	PMID:24239381	PCS		2/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000028	PMID:24239381	PCS		2/2			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:615663	Warburg micro syndrome 4		HP:0000501	PMID:24239381	PCS		6/6			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-05-02]
OMIM:601616	Iris pigment epithelium anomalies		HP:0011523	PMID:8874445	PCS					P	HPO:probinson[2018-06-13]
OMIM:601616	Iris pigment epithelium anomalies		HP:0000006	PMID:8874445	PCS					I	HPO:iea[2009-02-17]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0001265	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0000252	PMID:26685157	PCS	HP:0003593	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0002650	PMID:26685157	PCS	HP:0003577	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0004322	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0000490	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0010819	PMID:26685157	PCS	HP:0003621	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0002154	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0001263	PMID:26685157	PCS	HP:0003593	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0002151	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0000580	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0032794	PMID:26685157	PCS	HP:0003621	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0002490	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0025190	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0002092	PMID:26685157	PCS	HP:0003593	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0011421	PMID:26685157	PCS		1/1			C	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0012444	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0011470	PMID:26685157	PCS	HP:0003593	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0002827	PMID:26685157	PCS	HP:0003621	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0100806	PMID:26685157	PCS	HP:0003621	1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0000007	PMID:26685157	PCS					I	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0002119	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0001257	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0003128	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:619059	Mitochondrial complex IV deficiency, nuclear type 15		HP:0003348	PMID:26685157	PCS		1/1			P	HPO:probinson[2020-12-06]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0004325	PMID:28617965	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000286	PMID:28617965;PMID:29597095	PCS		2/3			P	HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000463	PMID:28617965	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000100	PMID:30079490	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0004322	PMID:28617965	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0001272	OMIM:618347	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0001250	PMID:30079490	PCS		0/4			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0003593	PMID:28617965	PCS		2/2			C	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0003073	OMIM:618347	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0001270	PMID:29597095	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0011461	PMID:29597095	PCS		1/1			C	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000733	PMID:28617965	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0002714	PMID:28617965;PMID:29597095	PCS		2/3			P	HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000218	OMIM:618347	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0001249	PMID:29597095;PMID:30079490	PCS		5/5			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0006855	PMID:28617965	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000154	PMID:28617965;PMID:29597095	PCS		2/3			P	HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000252	PMID:28617965;PMID:29597095;PMID:30079490	PCS		7/7			P	HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000750	PMID:28617965;PMID:29597095	PCS		3/3			P	HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0031936	PMID:28617965	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0002750	PMID:28617965	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0001263	PMID:28617965;PMID:30079490	PCS		6/6			P	HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000691	PMID:28617965	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000097	PMID:30079490	PCS		2/4			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000093	PMID:30079490	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000749	PMID:28617965	PCS		2/2			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000629	PMID:28617965;PMID:29597095	PCS		2/3			P	HPO:probinson[2022-03-11];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000007	PMID:28617965	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000821	PMID:30079490	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0000824	PMID:28617965	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0004209	PMID:30079490	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0001511	PMID:29597095	PCS		1/1			P	HPO:probinson[2022-03-11]
OMIM:618347	Galloway-Mowat syndrome 6		HP:0001510	PMID:28617965;PMID:29597095;PMID:30079490	PCS		7/7			P	HPO:probinson[2022-03-11]
OMIM:119570	Cleft soft palate		HP:0000185	OMIM:119570	IEA					P	HPO:iea[2009-02-17]
OMIM:119570	Cleft soft palate		HP:0000006	OMIM:119570	IEA					I	HPO:iea[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0004322	OMIM:608154	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0001250	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0031367	OMIM:608154	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0100864	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0009064	OMIM:608154	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0001508	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0000938	OMIM:608154	TAS				HP:0003676	P	HPO:skoehler[2013-06-10]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0007464	OMIM:608154	TAS					P	HPO:skoehler[2012-02-20]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0001547	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0002857	OMIM:608154	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0006257	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0001249	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0005328	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0000951	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0002215	OMIM:608154	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0002750	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0004993	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0000490	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0001518	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0000407	OMIM:608154	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0000327	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0000007	OMIM:608154	IEA					I	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0009059	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0100818	OMIM:608154	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0002967	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0001511	OMIM:608154	IEA					P	HPO:skoehler[2009-02-17]
OMIM:608154	Lipodystrophy, generalized, with impaired intellectual development, deafness, short stature, and slender bones		HP:0001533	OMIM:608154	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607501	Migraine without aura, susceptibility to, 4		HP:0002013	OMIM:607501	IEA					P	HPO:iea[2009-02-17]
OMIM:607501	Migraine without aura, susceptibility to, 4		HP:0000613	OMIM:607501	IEA					P	HPO:iea[2009-02-17]
OMIM:607501	Migraine without aura, susceptibility to, 4		HP:0002083	OMIM:607501	IEA					P	HPO:iea[2009-02-17]
OMIM:607501	Migraine without aura, susceptibility to, 4		HP:0002183	OMIM:607501	IEA					P	HPO:iea[2009-02-17]
OMIM:607501	Migraine without aura, susceptibility to, 4		HP:0002018	OMIM:607501	IEA					P	HPO:iea[2009-02-17]
OMIM:607501	Migraine without aura, susceptibility to, 4		HP:0000006	OMIM:607501	IEA					I	HPO:iea[2009-02-17]
OMIM:607501	Migraine without aura, susceptibility to, 4		HP:0001347	OMIM:607501	IEA					P	HPO:iea[2009-02-17]
OMIM:150170	Lactic acidosis, chronic adult form		HP:0004925	OMIM:150170	TAS					P	HPO:skoehler[2009-02-17]
OMIM:150170	Lactic acidosis, chronic adult form		HP:0000006	OMIM:150170	IEA					I	HPO:iea[2009-02-17]
OMIM:150170	Lactic acidosis, chronic adult form		HP:0002149	OMIM:150170	IEA					P	HPO:iea[2009-02-17]
OMIM:617712	Oocyte maturation defect 3		HP:0011462	PMID:28886344	PCS		6/6			C	HPO:probinson[2022-10-07]
OMIM:617712	Oocyte maturation defect 3		HP:0008222	PMID:28886344	PCS		6/6			P	HPO:probinson[2022-10-07]
OMIM:617712	Oocyte maturation defect 3		HP:0000006	PMID:28886344	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-10-07]
OMIM:611363	Atrial septal defect 4		HP:0001680	PMID:17668378	PCS		HP:0040283			P	HPO:probinson[2013-04-06]
OMIM:611363	Atrial septal defect 4		HP:0001631	PMID:17668378	PCS					P	HPO:probinson[2013-04-06]
OMIM:611363	Atrial septal defect 4		HP:0000006	PMID:17668378	PCS					I	HPO:probinson[2013-01-09]
OMIM:611363	Atrial septal defect 4		HP:0001655	PMID:17668378	PCS		HP:0040283			P	HPO:probinson[2013-04-06]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0002553	OMIM:102150	IEA					P	HPO:probinson[2009-02-17]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0001176	PMID:1619638	PCS		4/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0000340	PMID:1619638	PCS		5/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0001520	OMIM:102150	TAS					P	HPO:probinson[2009-02-17]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0009928	PMID:1619638	PCS		5/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0002002	PMID:1619638	PCS		5/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0002684	PMID:1619638	PCS		3/3			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0001382	PMID:1619638	PCS		5/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0000581	OMIM:102150	IEA					P	HPO:iea[2009-02-17]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0010047	PMID:1619638	PCS		3/3			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0001182	OMIM:102150	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0000506	PMID:1619638	PCS		5/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0011463	PMID:1619638	PCS		5/5			C	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0012471	PMID:1619638	PCS		4/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0001328	OMIM:102150	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0000414	PMID:1619638	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0000664	PMID:1619638	PCS		2/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0000006	PMID:1619638	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0001249	PMID:1619638	PCS		1/5			P	HPO:probinson[2022-07-01]
OMIM:102150	Acromegaloid facial appearance syndrome		HP:0000347	PMID:1619638	PCS		5/5			P	HPO:probinson[2022-07-01]
OMIM:183300	Splenogonadal fusion with limb defects and micrognathia		HP:0006283	OMIM:183300	IEA					P	HPO:iea[2009-02-17]
OMIM:183300	Splenogonadal fusion with limb defects and micrognathia		HP:0003826	OMIM:183300	IEA					C	HPO:skoehler[2010-06-20]
OMIM:183300	Splenogonadal fusion with limb defects and micrognathia		HP:0006333	OMIM:183300	IEA					P	HPO:iea[2009-02-17]
OMIM:183300	Splenogonadal fusion with limb defects and micrognathia		HP:0000119	OMIM:183300	IEA					P	HPO:iea[2009-02-17]
OMIM:183300	Splenogonadal fusion with limb defects and micrognathia		HP:0000006	OMIM:183300	IEA					I	HPO:iea[2009-02-17]
OMIM:183300	Splenogonadal fusion with limb defects and micrognathia		HP:0000347	OMIM:183300	IEA					P	HPO:iea[2009-02-17]
OMIM:620196	Spermatogenic failure 79		HP:0032560	PMID:34980136	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:620196	Spermatogenic failure 79		HP:0003251	PMID:34980136	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:620196	Spermatogenic failure 79		HP:0011462	PMID:34980136	PCS		1/1			C	HPO:probinson[2023-04-11]
OMIM:620196	Spermatogenic failure 79		HP:0000007	PMID:34980136	PCS					I	HPO:probinson[2023-04-11]
OMIM:620196	Spermatogenic failure 79		HP:0012207	PMID:34980136	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:620196	Spermatogenic failure 79		HP:0000798	PMID:34980136	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000286	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0002465	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0005216	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000341	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0002002	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0030674	PMID:34230638	PCS		3/5			C	HPO:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0002066	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001252	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0003593	PMID:34230638	PCS		1/5			C	HPO:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001290	PMID:34230638	PCS		2/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001629	PMID:34230638	PCS		2/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000737	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000938	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000717	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000954	PMID:34230638	PCS		2/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001643	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001763	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001249	PMID:34230638	PCS		3/3			P	HP:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000215	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000358	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001347	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0003623	PMID:34230638	PCS		1/5			C	HPO:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0002311	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000494	PMID:34230638	PCS		2/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0002650	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0011968	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0002033	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001263	PMID:34230638	PCS		5/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000350	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0032988	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0100023	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0100710	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000007	PMID:34230638	PCS					I	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0001558	PMID:34230638	PCS		2/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0004209	PMID:34230638	PCS		2/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0002307	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000268	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000369	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:619717	Intellectual developmental disorder, autosomal recessive 73		HP:0000687	PMID:34230638	PCS		1/5			P	HP:probinson[2022-03-07]
OMIM:107000	Nail disorder, nonsyndromic congenital, 6		HP:0001374	OMIM:107000	IEA					P	HPO:iea[2009-02-17]
OMIM:107000	Nail disorder, nonsyndromic congenital, 6		HP:0002164	OMIM:107000	IEA					P	HPO:iea[2009-02-17]
OMIM:107000	Nail disorder, nonsyndromic congenital, 6		HP:0009884	OMIM:107000	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:107000	Nail disorder, nonsyndromic congenital, 6		HP:0008404	OMIM:107000	TAS					P	HPO:skoehler[2013-05-03]
OMIM:107000	Nail disorder, nonsyndromic congenital, 6		HP:0000006	OMIM:107000	IEA					I	HPO:iea[2009-02-17]
OMIM:107000	Nail disorder, nonsyndromic congenital, 6		HP:0001798	OMIM:107000	IEA					P	HPO:iea[2009-02-17]
OMIM:612642	Deafness, autosomal dominant 59		HP:0003577	PMID:19030898	PCS		14/14			C	HPO:probinson[2022-07-02]
OMIM:612642	Deafness, autosomal dominant 59		HP:0000407	PMID:19030898	PCS	HP:0003577	14/14		HP:0012828	P	HPO:probinson[2019-01-16];HPO:probinson[2022-07-02]
OMIM:612642	Deafness, autosomal dominant 59		HP:0000006	PMID:19030898	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-01-16]
OMIM:614233	Hyperpigmentation, familial progressive, 1		HP:0000953	PMID:16709486	PCS					P	HPO:probinson[2017-06-23]
OMIM:614233	Hyperpigmentation, familial progressive, 1		HP:0000006	PMID:16709486	PCS					I	HPO:probinson[2017-06-23]
DECIPHER:51	2q33.1 deletion syndrome		HP:0000708	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:51	2q33.1 deletion syndrome		HP:0000175	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:51	2q33.1 deletion syndrome		HP:0000023	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:51	2q33.1 deletion syndrome		HP:0004322	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:51	2q33.1 deletion syndrome		HP:0001250	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:51	2q33.1 deletion syndrome		HP:0008872	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:51	2q33.1 deletion syndrome		HP:0000218	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:51	2q33.1 deletion syndrome		HP:0001249	DECIPHER:51	IEA					P	HPO:skoehler[2013-05-29]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0003015	OMIM:187600	TAS					P	HPO:probinson[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0003577	PMID:21253318	PCS		1/1			C	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0004565	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0002089	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0002980	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0005257	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0008909	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0001252	OMIM:187600	TAS					P	HPO:probinson[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0002282	OMIM:187600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0011220	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0034222	PMID:24585534	PCS		6/20			P	HPO:probinson[2023-07-18]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000910	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0008873	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000238	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000774	PMID:21253318	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000773	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000256	PMID:21253318	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0002676	OMIM:187600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0001623	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0002677	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0003026	PMID:21253318	PCS		1/1		HP:0012828	P	HPO:probinson[2012-05-05];HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000274	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0001561	PMID:21253318	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0008839	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0003025	OMIM:187600	TAS					P	HPO:probinson[2015-03-21]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0003185	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0001263	OMIM:187600	IEA					P	HPO:skoehler[2015-01-21]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000470	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0030928	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0011800	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0034226	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0030921	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000946	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000926	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0006584	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0001558	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0006487	OMIM:187600	TAS					P	HPO:probinson[2012-05-05]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0001538	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0003811	OMIM:187600	IEA					C	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0002007	OMIM:187600	IEA					P	HPO:iea[2009-02-17]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0002643	PMID:21253318	PCS		1/1			P	HPO:probinson[2022-04-15]
OMIM:187600	Thanatophoric dysplasia, type I		HP:0000006	OMIM:187600	IEA					I	HPO:iea[2009-02-17]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0001100	PMID:10851256	PCS		0/11			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0003577	PMID:10851256	PCS		11/11			C	HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0000635	PMID:10851256	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0007894	PMID:10851256	PCS		11/11			P	HPO:probinson[2015-07-19];HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0002227	PMID:10851256	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0007513	PMID:10851256	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0000006	PMID:10851256	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0008527	PMID:10851256	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:103500	Tietz albinism-deafness syndrome		HP:0002226	PMID:10851256	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-18]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0034386	PMID:12642359	PCS		5/8			P	HPO:probinson[2022-10-07]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0001639	PMID:12642359	PCS		8/8			P	HPO:probinson[2022-07-04]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0005144	PMID:12642359	PCS		5/8			P	HPO:probinson[2022-07-04]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0003581	PMID:12642359	PCS		8/8			C	HPO:probinson[2022-07-04]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0004757	PMID:12642359	PCS		1/8			P	HPO:probinson[2013-03-10];HPO:probinson[2022-07-04]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0000006	PMID:12642359	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-07-04]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0001645	PMID:12642359	PCS		2/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-04]
OMIM:612124	Cardiomyopathy, familial hypertrophic, 12		HP:0004756	PMID:12642359	PCS		2/8			P	HPO:probinson[2013-03-10];HPO:probinson[2022-07-04]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0000253	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0001276	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0000473	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0002510	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0002650	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0003487	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0002376	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0001332	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0002079	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0011968	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0001272	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0012706	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0012708	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0000280	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0000737	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0011463	PMID:32128616	PCS		1/1			C	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0000508	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0012450	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0000007	PMID:32128616	PCS					I	HPO:probinson[2020-12-12];HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0030081	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0001007	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:619071	Leukodystrophy, hypomyelinating, 20		HP:0001348	PMID:32128616	PCS		1/1			P	HPO:probinson[2020-12-12]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0003577	PMID:25560765	PCS		10/10			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001250	PMID:25560765	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001274	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0031882	PMID:25560765	PCS		10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0002714	PMID:25560765	PCS		10/10			P	HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001522	PMID:25560765	PCS					C	HPO:probinson[2022-09-23];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001004	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001007	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001188	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0000252	PMID:25560765	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001321	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0000293	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001263	PMID:25560765	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0000350	PMID:25560765	PCS		10/10			P	HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0002151	PMID:25560765	PCS		0/10			P	HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001284	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0000470	PMID:25560765	PCS					P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0000294	PMID:25560765	PCS		10/10			P	HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0010851	PMID:25560765	PCS		3/3			P	HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0011922	PMID:25560765	PCS		0/10			P	HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0032988	PMID:25560765	PCS		10/10			P	HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0001339	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0002804	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0000007	PMID:25560765	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0003811	PMID:25560765	PCS					C	HPO:probinson[2022-09-23];HPO:probinson[2022-09-23]
OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia		HP:0000347	PMID:25560765	PCS		10/10			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-23]
OMIM:610733	Noonan syndrome 4		HP:0000286	PMID:18925667	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001892	PMID:17143282;PMID:18925667	PCS		6/17			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0004322	PMID:17143282;PMID:17143285;PMID:17586837	PCS		19/53			P	HPO:probinson[2021-05-20];HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0045075	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001929	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001629	PMID:17143285;PMID:18925667	PCS		2/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0012471	PMID:17143282;PMID:18925667	PCS		15/17			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000915	OMIM:610733	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610733	Noonan syndrome 4		HP:0011461	PMID:18925667	IEA		1/1			C	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000316	PMID:18925667	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000635	PMID:18925667	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000978	PMID:17143285;PMID:17586837	PCS		8/38			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0006610	PMID:18925667	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001642	PMID:17143282;PMID:17143285;PMID:17586837;PMID:18925667	PCS		40/55			P	HPO:probinson[2021-05-20];HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000256	PMID:17143282	PCS		9/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0001488	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000358	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001249	PMID:17143282;PMID:17586837	PCS		6/40			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0003645	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000154	PMID:17143282	PCS		14/16			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0003125	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0002212	PMID:17143282;PMID:18925667	PCS		15/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001561	PMID:17143282	PCS	HP:0011461	8/15			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0001561	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000494	PMID:17143282	PCS		15/16			P	HPO:skoehler[2012-11-20];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0002650	PMID:18925667	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001520	PMID:17143282	PCS	HP:0011461	9/15			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0002750	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000073	PMID:17143285	PCS		1/13			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000391	PMID:17143282;PMID:18925667	PCS		17/17			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000470	PMID:17143282	PCS		15/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0005280	PMID:18925667	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0009890	OMIM:610733	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610733	Noonan syndrome 4		HP:0032152	PMID:17143282;PMID:18925667	PCS		9/17			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0001639	PMID:17143282;PMID:17143285;PMID:17586837	PCS		6/54			P	HPO:probinson[2021-05-20];HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000508	PMID:17143282	PCS		16/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000767	PMID:18925667	PCS		1/1			P	HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000689	OMIM:610733	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610733	Noonan syndrome 4		HP:0000766	PMID:17143282	PCS		16/16			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0002967	OMIM:610733	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610733	Noonan syndrome 4		HP:0000465	PMID:17143282	PCS		15/16			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0001873	PMID:17143285	PCS		2/13			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0001631	PMID:17143285;PMID:17586837	PCS		6/38			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000369	PMID:17143282;PMID:18925667	PCS		17/17			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-22]
OMIM:610733	Noonan syndrome 4		HP:0000028	PMID:17143282	PCS		6/9			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000028	PMID:17586837	PCS		5/11			P	HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000028	PMID:17143285	PCS		5/9	MALE		P	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000006	PMID:17143285	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-05-20]
OMIM:610733	Noonan syndrome 4		HP:0000126	PMID:17143285	PCS		1/13			P	HPO:probinson[2021-05-20]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0002069	PMID:23746447	PCS		1/4			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0001264	PMID:23746447	PCS					P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0003577	PMID:23746447	PCS		4/4			C	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0000750	PMID:23746447	PCS		4/4			P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0001531	PMID:23746447	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0001332	PMID:23746447	PCS		3/4			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0004322	PMID:23746447	PCS					P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0003487	PMID:23746447	PCS					P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0001251	PMID:23746447	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0002490	PMID:23746447	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0001270	PMID:23746447	PCS		2/4			P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0012240	PMID:23746447	PCS		3/3			P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0000007	PMID:23746447	PCS					I	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0008347	PMID:23746447	PCS					P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0001348	PMID:23746447	PCS					P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0003688	PMID:23746447	PCS		1/1			P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0003128	PMID:23746447	PCS	HP:0003577	4/4			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0001336	PMID:23746447	PCS		1/4			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0500233	PMID:23746447	PCS					P	HPO:probinson[2020-12-08]
OMIM:619065	Mitochondrial complex IV deficiency, nuclear type 21		HP:0003557	PMID:23746447	PCS					P	HPO:probinson[2020-12-08]
OMIM:615887	Amelogenesis imperfecta, type IIA5		HP:0000670	PMID:24621671	PCS		1/1			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-01-28]
OMIM:615887	Amelogenesis imperfecta, type IIA5		HP:0000705	PMID:23375655;PMID:24621671	PCS		6/6			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-01-28];HPO:probinson[2023-01-28]
OMIM:615887	Amelogenesis imperfecta, type IIA5		HP:0002164	PMID:24621671	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:615887	Amelogenesis imperfecta, type IIA5		HP:0011463	PMID:24621671	PCS		1/1			C	HPO:probinson[2023-01-28]
OMIM:615887	Amelogenesis imperfecta, type IIA5		HP:0006286	PMID:23375655;PMID:24621671	PCS		6/6			P	HPO:probinson[2023-01-28]
OMIM:615887	Amelogenesis imperfecta, type IIA5		HP:0000007	PMID:23375655	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-28]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000286	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000582	PMID:8230159	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000260	PMID:8230159	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0001252	OMIM:614541;PMID:8230159	PCS		15/16			P	HPO:probinson[2021-06-26];HPO:skoehler[2014-11-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000581	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0012745	PMID:8230159	PCS		1/6			P	HPO:skoehler[2014-03-24];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0001508	PMID:8230159	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0010055	PMID:8230159	PCS		4/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000316	PMID:8230159	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000954	PMID:8230159	PCS		2/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0008897	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000218	PMID:8230159	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0006610	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0003745	PMID:8230159	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000774	PMID:8230159	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000358	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0002553	PMID:8230159	PCS		1/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000252	PMID:8230159	IEA		3/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0001385	PMID:8230159	PCS		1/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000431	PMID:8230159	PCS		3/6			P	HPO:skoehler[2013-06-12];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0005487	PMID:8230159	PCS		2/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0002033	PMID:8230159	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0001263	PMID:8230159	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000470	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0005280	OMIM:614541	TAS					P	HPO:skoehler[2013-08-11]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0001518	PMID:8230159	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000407	PMID:8230159	PCS		1/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000348	PMID:8230159	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0002645	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0002007	OMIM:614541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0001510	PMID:8230159	PCS		6/6			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000047	PMID:8230159	PCS		1/2			P	HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000347	PMID:8230159	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000369	PMID:8230159	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:614541	Chromosome 16q22 deletion syndrome		HP:0000028	PMID:8230159	PCS		2/2			P	HPO:probinson[2021-06-26]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002123	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0010808	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0000160	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002240	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001251	OMIM:230600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001290	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0000280	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0012368	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0007281	OMIM:230600	TAS					P	HPO:probinson[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001508	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0011463	PMID:30187681	PCS		1/1			C	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002119	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0008479	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001643	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0000212	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002753	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001744	PMID:30187681	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001622	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002510	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0009826	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002015	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002059	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001982	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002650	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001387	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0001288	PMID:30187681	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0002673	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0007272	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0033044	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0000926	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0008166	PMID:30187681	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0000943	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0005619	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:230600	GM1-gangliosidosis, type II		HP:0000007	OMIM:230600	IEA					I	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0000648	OMIM:230600	IEA					P	HPO:iea[2009-02-17]
OMIM:230600	GM1-gangliosidosis, type II		HP:0004568	PMID:30187681	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:612656	Episodic ataxia, type 6		HP:0002301	OMIM:612656	IEA					P	HPO:skoehler[2013-01-09]
OMIM:612656	Episodic ataxia, type 6		HP:0000571	OMIM:612656	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0000651	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0002078	PMID:16116111	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-09-29]
OMIM:612656	Episodic ataxia, type 6		HP:0001321	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0002321	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0002013	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0002131	PMID:16116111	PCS		1/1		HP:0025215	P	HPO:skoehler[2013-01-09];HPO:probinson[2022-09-29]
OMIM:612656	Episodic ataxia, type 6		HP:0002076	OMIM:612656	IEA					P	HPO:skoehler[2013-01-09]
OMIM:612656	Episodic ataxia, type 6		HP:0001250	OMIM:612656	IEA					P	HPO:skoehler[2013-01-09]
OMIM:612656	Episodic ataxia, type 6		HP:0001272	PMID:16116111	PCS		1/1			P	HPO:probinson[2022-09-29]
OMIM:612656	Episodic ataxia, type 6		HP:0001260	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0001350	PMID:16116111	PCS		1/1		HP:0025215	P	HPO:skoehler[2013-01-09];HPO:probinson[2022-09-29]
OMIM:612656	Episodic ataxia, type 6		HP:0003593	PMID:16116111	PCS		1/1			C	HPO:probinson[2022-09-29]
OMIM:612656	Episodic ataxia, type 6		HP:0002183	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0001270	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0000639	OMIM:612656	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0000613	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0001269	PMID:16116111	PCS		1/1		HP:0025215	P	HPO:skoehler[2013-01-09];HPO:probinson[2022-09-29]
OMIM:612656	Episodic ataxia, type 6		HP:0002018	OMIM:612656	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612656	Episodic ataxia, type 6		HP:0006852	PMID:16116111	PCS	HP:0003593	1/1			P	HPO:probinson[2022-09-29]
OMIM:612656	Episodic ataxia, type 6		HP:0000006	PMID:16116111	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-29]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0002850	PMID:23230001	PCS		14/14			P	HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0002653	PMID:23230001	PCS		3/14			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0003577	PMID:23230001	PCS					C	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0004322	PMID:23230001	PCS		12/13			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0002783	PMID:23230001	PCS		11/14			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0002110	PMID:23230001	PCS		2/14			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0000272	PMID:23230001	PCS		11/14			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0004482	PMID:23230001	PCS					P	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0031367	PMID:23230001	PCS		1/14			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0033832	PMID:23230001	PCS		10/14			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0000007	PMID:23230001	PCS					I	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0000337	PMID:23230001	PCS		11/14			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0007421	PMID:23230001	PCS		11/14			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0002788	PMID:23230001	PCS		11/14			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:615139	Facial dysmorphism, immunodeficiency, livedo, and short stature		HP:0002721	PMID:23230001	PCS		12/14			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-09-06]
OMIM:614227	Hyperuricemic nephropathy, familial juvenile, 3		HP:0032581	OMIM:614227	TAS					P	HPO:probinson[2022-09-29]
OMIM:614227	Hyperuricemic nephropathy, familial juvenile, 3		HP:0000083	OMIM:614227	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614227	Hyperuricemic nephropathy, familial juvenile, 3		HP:0004727	OMIM:614227	TAS					P	HPO:probinson[2022-09-29]
OMIM:614227	Hyperuricemic nephropathy, familial juvenile, 3		HP:0000006	OMIM:614227	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614227	Hyperuricemic nephropathy, familial juvenile, 3		HP:0002149	OMIM:614227	TAS					P	HPO:probinson[2022-09-29]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002540	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002066	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000160	PMID:17088400	PCS			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002020	PMID:17088400	PCS			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0001508	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000716	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			FEMALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000717	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000739	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0008872	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000733	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002019	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000252	PMID:17088400	PCS			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002015	PMID:17088400	PCS			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000750	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0001344	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002079	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0001263	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000272	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002191	PMID:17088400	PCS	HP:0003621		MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0005280	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0003819	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		C	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0001419	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA					I	HPO:iea[2010-09-13]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0001319	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-13]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000009	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002307	PMID:17088400	PCS			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002205	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000400	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0000248	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA			MALE		P	HPO:iea[2010-09-15]
DECIPHER:45	Xq28 (MECP2) duplication		HP:0002720	PMID:17088400	PCS	HP:0003621		MALE		P	HPO:iea[2010-09-15]
OMIM:147430	Marsili syndrome		HP:0002661	PMID:29253101	PCS					P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0007021	PMID:29253101	PCS	HP:0003593	6/6			P	HPO:skoehler[2010-06-18];HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0008000	PMID:29253101	PCS		6/6			P	HPO:lccarmody[2018-10-04];HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0010829	PMID:29253101	PCS	HP:0003593	6/6			P	HPO:lccarmody[2018-10-04];HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0001954	PMID:29253101	PCS		15/16			P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0000559	PMID:29253101	PCS		0/6			P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0000966	PMID:29253101	PCS					P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0002315	PMID:29253101	PCS					P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0000006	PMID:29253101	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-08]
OMIM:147430	Marsili syndrome		HP:0000632	PMID:29253101	PCS		0/6			P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-08]
OMIM:600252	Lowry-Maclean syndrome		HP:0000175	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0000252	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0001363	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0004467	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0000684	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0001263	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0009110	OMIM:600252	TAS					P	HPO:probinson[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0001627	OMIM:600252	TAS					P	HPO:lccarmody[2018-10-18]
OMIM:600252	Lowry-Maclean syndrome		HP:0000444	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0001511	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0000501	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0001249	OMIM:600252	IEA					P	HPO:iea[2009-02-17]
OMIM:600252	Lowry-Maclean syndrome		HP:0000006	OMIM:600252	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0003577	PMID:25754315	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000343	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0004322	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000463	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0001272	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0003196	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0001290	PMID:25754315	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0011951	PMID:25754315	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0012110	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0001508	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000319	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0011220	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0012450	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000316	PMID:25754315	PCS		1/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0002119	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0002059	PMID:25754315	PCS		1/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000431	PMID:25754315	PCS		1/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0011968	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0001263	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05];HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0034323	PMID:25754315	PCS		2/2			P	HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0005280	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0030746	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000407	PMID:25754315	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000007	PMID:25754315	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000768	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0001159	PMID:25754315	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:616430	Combined oxidative phosphorylation deficiency 25		HP:0000369	PMID:25754315	PCS		2/2			P	HPO:skoehler[2015-07-05]
OMIM:105830	Angelman syndrome		HP:0000486	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0002120	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0001250	PMID:8929945	PCS		26/27			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0002286	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0010808	OMIM:105830	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105830	Angelman syndrome		HP:0001010	PMID:8929945	PCS		19/26			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0001252	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0001251	PMID:8929945	PCS		27/27			P	HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0001290	OMIM:105830	TAS					P	HPO:skoehler[2017-07-13]
OMIM:105830	Angelman syndrome		HP:0001270	PMID:8929945	PCS		27/27			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0040082	PMID:8929945	PCS		27/27			P	HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0000639	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0007240	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0000635	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0008872	PMID:8929945	PCS		20/26			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0000752	OMIM:105830	PCS					P	HPO:iea[2009-12-03]
OMIM:105830	Angelman syndrome		HP:0000158	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0003745	OMIM:105830	TAS		HP:0040282			I	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0002019	OMIM:105830	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0000577	OMIM:105830	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105830	Angelman syndrome		HP:0001347	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0200085	OMIM:105830	TAS					P	HPO:skoehler[2013-06-04]
OMIM:105830	Angelman syndrome		HP:0005469	OMIM:105830	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0000154	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0002136	OMIM:105830	TAS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0002312	OMIM:105830	TAS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0001344	PMID:8929945	PCS		27/27			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0002353	ISBN-13:978-0721606156;PMID:8929945	PCS		35/35			P	HPO:probinson[2023-06-04];HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0002650	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0006979	PMID:8929945	PCS		18/21			P	HPO:iea[2009-12-03];HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0031936	PMID:8929945	PCS		22/22			P	HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0000490	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0001263	PMID:8929945	PCS		27/27			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-06-04]
OMIM:105830	Angelman syndrome		HP:0005484	OMIM:105830	PCS		20/20			P	HPO:probinson[2012-05-01];HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0000749	OMIM:105830	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0000327	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0002307	OMIM:105830	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105830	Angelman syndrome		HP:0000006	OMIM:105830	PCS					I	HPO:iea[2009-12-03]
OMIM:105830	Angelman syndrome		HP:0000248	OMIM:105830	TAS					P	HPO:probinson[2012-05-01]
OMIM:105830	Angelman syndrome		HP:0000303	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0000545	OMIM:105830	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105830	Angelman syndrome		HP:0001513	OMIM:105830	PCS					P	HPO:iea[2009-02-17]
OMIM:105830	Angelman syndrome		HP:0000687	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0002069	PMID:15174025	PCS		4/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0200072	PMID:15174025	PCS		5/5			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0001266	PMID:15174025	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0001332	PMID:15174025	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0002376	PMID:15174025	PCS		1/5			P	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0000639	PMID:15174025	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0012194	PMID:15174025	PCS		5/5			P	HPO:probinson[2013-03-14];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0011463	PMID:15174025	PCS		4/4			C	HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0002315	PMID:15174025	PCS		0/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0000006	PMID:15174025	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:104290	Alternating hemiplegia of childhood 1		HP:0001249	PMID:15174025	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-06]
OMIM:243605	Stromme syndrome		HP:0003577	OMIM:243605	IEA					C	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0005235	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0003198	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0002000	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0001274	PMID:25564561	PCS					P	HPO:probinson[2017-06-20]
OMIM:243605	Stromme syndrome		HP:0000482	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0012841	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000518	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0003826	PMID:25564561	PCS					C	HPO:probinson[2017-06-20]
OMIM:243605	Stromme syndrome		HP:0000316	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000612	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000238	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000659	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0001747	OMIM:243605	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:243605	Stromme syndrome		HP:0001320	PMID:25564561	PCS					P	HPO:probinson[2017-06-20]
OMIM:243605	Stromme syndrome		HP:0000154	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000175	PMID:25564561	PCS					P	HPO:probinson[2017-06-20]
OMIM:243605	Stromme syndrome		HP:0000252	OMIM:243605	IEA					P	HPO:skoehler[2019-04-18]
OMIM:243605	Stromme syndrome		HP:0000431	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0001321	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000490	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0012584	PMID:25564561	PCS					P	HPO:probinson[2017-06-20]
OMIM:243605	Stromme syndrome		HP:0000609	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0100258	OMIM:243605	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:243605	Stromme syndrome		HP:0000426	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000007	PMID:25564561	PCS					I	HPO:probinson[2017-06-20]
OMIM:243605	Stromme syndrome		HP:0000568	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000647	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0002247	PMID:25564561	PCS					P	HPO:probinson[2017-06-20]
OMIM:243605	Stromme syndrome		HP:0002566	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243605	Stromme syndrome		HP:0000369	OMIM:243605	IEA					P	HPO:skoehler[2019-04-18]
OMIM:243605	Stromme syndrome		HP:0000347	OMIM:243605	IEA					P	HPO:skoehler[2019-04-18]
OMIM:243605	Stromme syndrome		HP:0000126	OMIM:243605	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0002344	PMID:30635937	PCS		2/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0003621	PMID:30635937	PCS		1/2			C	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0001310	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0001272	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0002373	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0001260	PMID:30635937	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0001251	PMID:30635937	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0001290	PMID:30635937	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0002490	PMID:30635937	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0012229	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:6000468	PMID:30635937	PCS		1/2			P	HPO:probinson[2024-04-03]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0034649	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0012402	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0011463	PMID:30635937	PCS		1/2			C	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0000007	PMID:30635937	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0002329	PMID:30635937	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0002500	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:618384	Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate		HP:0033092	PMID:30635937	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0200070	OMIM:136550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0008002	OMIM:136550	TAS					P	HPO:skoehler[2010-06-20]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0003593	PMID:1685483	PCS					C	HPO:probinson[2024-03-08]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0007641	PMID:1685483	PCS		0/75			P	HPO:probinson[2012-07-24];HPO:probinson[2024-03-08]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0007663	PMID:27777503	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-20]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0011510	OMIM:136550	TAS					P	HPO:probinson[2015-07-19]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0000603	OMIM:136550	TAS					P	HPO:skoehler[2017-07-13]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0007754	PMID:27777503	PCS		6/6			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:136550	Macular dystrophy, retinal, 1, north Carolina type		HP:0000006	PMID:27777503	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:609289	Syncope, familial vasovagal		HP:0002321	OMIM:609289	TAS					P	HPO:skoehler[2015-02-22]
OMIM:609289	Syncope, familial vasovagal		HP:0001279	OMIM:609289	IEA					P	HPO:skoehler[2015-12-30]
OMIM:609289	Syncope, familial vasovagal		HP:0000006	OMIM:609289	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0003676	PMID:25921221	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0001399	PMID:25921221;PMID:24614073	PCS		11/14			P	HPO:probinson[2021-02-25];HPO:skoehler[2014-08-24];HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0001409	PMID:24614073	TAS		2/12			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0001394	PMID:25921221	PCS		2/2			P	HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0003593	PMID:25921221	IEA		1/2			C	HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0000007	PMID:24614073	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0001406	PMID:25921221;PMID:24614073	PCS		14/14			P	HPO:probinson[2021-02-25];HPO:skoehler[2014-08-24];HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0001402	PMID:25921221	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-25]
OMIM:615878	Cholestasis, progressive familial intrahepatic 4		HP:0003623	PMID:25921221	PCS		1/2			C	HPO:probinson[2021-02-25]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0005403	PMID:10700239	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0002850	PMID:11145714	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0004313	PMID:10700239	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0003593	PMID:11145714;PMID:10700239	PCS		2/2			C	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0010976	PMID:11145714	PCS		0/1			P	HPO:probinson[2022-08-06];HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0003819	PMID:10700239	PCS		1/1			C	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0002849	PMID:10700239	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0000007	PMID:10700239	PCS					I	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0012191	PMID:10700239	PCS	HP:0011463	1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0001888	PMID:11145714	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0001945	PMID:11145714	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0000988	PMID:11145714	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0001433	PMID:11145714	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0003347	PMID:10700239	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0002720	PMID:11145714;PMID:10700239	PCS		2/2			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0001876	PMID:11145714	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0005404	PMID:10700239	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0040218	PMID:10700239	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:619924	Immunodeficiency 105, severe combined		HP:0004315	PMID:11145714;PMID:10700239	PCS		2/2			P	HPO:probinson[2022-08-06]
DECIPHER:92	Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)		HP:0000252	DECIPHER:92	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:92	Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)		HP:0000750	DECIPHER:92	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:92	Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)		HP:0001249	DECIPHER:92	IEA					P	HPO:skoehler[2013-05-29]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0002960	OMIM:137100	IEA					P	HPO:iea[2009-02-17]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0004798	OMIM:137100	TAS					P	HPO:skoehler[2013-05-29]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0002024	OMIM:137100	IEA					P	HPO:iea[2009-02-17]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0002719	OMIM:137100	IEA					P	HPO:iea[2009-02-17]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0000007	OMIM:137100	TAS					I	HPO:skoehler[2012-10-17]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0002205	OMIM:137100	TAS					P	HPO:skoehler[2012-11-21]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0003745	OMIM:137100	TAS					I	HPO:skoehler[2015-12-30]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0002720	OMIM:137100	IEA					P	HPO:iea[2009-02-17]
OMIM:137100	Immunoglobulin A deficiency 1		HP:0000006	OMIM:137100	TAS					I	HPO:skoehler[2012-10-17]
OMIM:617921	Amyotrophic lateral sclerosis, susceptibility to, 25		HP:0003596	PMID:29566793	PCS		11/12			C	HPO:probinson[2022-11-26]
OMIM:617921	Amyotrophic lateral sclerosis, susceptibility to, 25		HP:0011462	PMID:29566793	PCS		1/12			C	HPO:probinson[2022-11-26]
OMIM:617921	Amyotrophic lateral sclerosis, susceptibility to, 25		HP:0003829	OMIM:617921	IEA					I	HPO:skoehler[2018-10-08]
OMIM:617921	Amyotrophic lateral sclerosis, susceptibility to, 25		HP:0007354	PMID:29566793	PCS		12/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:617921	Amyotrophic lateral sclerosis, susceptibility to, 25		HP:0000006	PMID:29566793	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:620155	Rabin-Pappas syndrome		HP:0000582	PMID:32710489	PCS		5/7			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001531	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000541	PMID:32710489	PCS		5/10			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001250	PMID:32710489	PCS		7/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001252	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0012745	PMID:32710489	PCS		8/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0005490	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0012110	PMID:32710489	PCS		8/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000518	PMID:32710489	PCS		2/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000717	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001548	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000316	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000238	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0007763	PMID:32710489	PCS		8/10			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0002779	PMID:32710489	PCS		2/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0009765	PMID:32710489	PCS		9/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000455	PMID:32710489	PCS		9/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000278	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001249	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0002553	PMID:32710489	PCS		11/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000252	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000494	PMID:32710489	PCS		0/7			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000431	PMID:32710489	PCS		9/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000276	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0002079	PMID:32710489	PCS		9/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001321	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0002791	PMID:32710489	PCS		9/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0011968	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001263	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000272	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000609	PMID:32710489	PCS		3/10			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000407	PMID:32710489	PCS		6/8			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0007099	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000629	PMID:32710489	PCS		8/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0002902	PMID:32710489	PCS		8/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000307	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000405	PMID:32710489	PCS		7/8			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000006	PMID:32710489	PCS					I	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0001513	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000303	PMID:32710489	PCS		0/12			P	HPO:probinson[2023-06-07]
OMIM:620155	Rabin-Pappas syndrome		HP:0000347	PMID:32710489	PCS		12/12			P	HPO:probinson[2023-06-07]
OMIM:300700	Albinism-deafness syndrome		HP:0001022	OMIM:300700	IEA					P	HPO:skoehler[2015-01-27]
OMIM:300700	Albinism-deafness syndrome		HP:0007509	OMIM:300700	IEA					P	HPO:iea[2009-02-17]
OMIM:300700	Albinism-deafness syndrome		HP:0001107	PMID:2349949	PCS		0/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:300700	Albinism-deafness syndrome		HP:0001417	PMID:2349949	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:300700	Albinism-deafness syndrome		HP:0007544	PMID:2349949	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:300700	Albinism-deafness syndrome		HP:0008527	OMIM:300700	IEA					P	HPO:iea[2009-02-17]
OMIM:300066	Deafness, X-linked 4		HP:0005101	OMIM:300066	TAS					P	HPO:probinson[2009-02-17]
OMIM:300066	Deafness, X-linked 4		HP:0000407	OMIM:300066	TAS					P	HPO:probinson[2013-03-10]
OMIM:300066	Deafness, X-linked 4		HP:0011463	OMIM:300066	TAS					C	HPO:probinson[2013-03-10]
OMIM:300066	Deafness, X-linked 4		HP:0001423	OMIM:300066	TAS					I	HPO:probinson[2013-03-10]
OMIM:116870	Celiac artery stenosis from compression by median arcuate ligamentof diaphragm		HP:0012327	OMIM:116870	TAS					P	HPO:iea[2013-08-13]
OMIM:116870	Celiac artery stenosis from compression by median arcuate ligamentof diaphragm		HP:0000006	OMIM:116870	TAS					I	HPO:iea[2009-02-17]
OMIM:116870	Celiac artery stenosis from compression by median arcuate ligamentof diaphragm		HP:0002027	OMIM:116870	TAS					P	HPO:iea[2009-02-17]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002301	PMID:24552284	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001297	PMID:27444081;PMID:26867732;PMID:24552284	PCS		12/15			P	HPO:probinson[2020-11-28];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001894	PMID:24552284	PCS		3/5			P	HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001251	PMID:24552284	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0003593	PMID:26867732	PCS		5/9			C	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0025343	PMID:26867732;PMID:24552284	PCS		5/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002381	PMID:27444081	PCS		1/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0100651	PMID:26867732	PCS		1/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001409	PMID:24552284	PCS		1/5			P	HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0011463	PMID:26867732	PCS		1/9			C	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001888	PMID:27059682	PCS		6/15			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000713	OMIM:615688	TAS					P	HPO:skoehler[2014-04-13]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0005528	PMID:26867732	PCS		1/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000872	PMID:26867732	PCS		1/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001369	PMID:26867732	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0003623	PMID:26867732	PCS		1/9			C	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001644	PMID:26867732	PCS		1/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0003565	PMID:27444081	PCS		1/1			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0011968	PMID:26867732	PCS		2/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:6000562	PMID:24552285	PCS		5/5			P	HPO:probinson[2024-04-03]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0012219	PMID:27444081;PMID:26867732;PMID:24552285	PCS		4/34			P	HPO:probinson[2020-11-28];HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0033260	PMID:27059682	PCS		11/15			P	HPO:probinson[2020-12-07]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0033261	PMID:27059682	PCS		3/15			P	HPO:probinson[2020-12-07]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002829	PMID:26867732	PCS		3/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000965	PMID:26867732;PMID:24552284	PCS		13/19			P	HPO:probinson[2020-11-28];HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000602	PMID:24552284	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0030351	PMID:24552284	PCS		3/5			P	HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000007	PMID:24552284	PCS					I	HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000403	PMID:27444081	PCS		1/1			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000964	PMID:26867732	PCS		5/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000648	PMID:27059682	PCS		1/15			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002027	PMID:24552285	PCS					P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001974	PMID:24552285	PCS		1/15			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002240	PMID:26867732;PMID:24552284	PCS		11/14			P	HPO:probinson[2020-11-28];HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002040	PMID:24552284	PCS		1/5			P	HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002719	PMID:26867732	PCS		3/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001903	PMID:24552284	PCS		HP:0040283			P	HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000979	PMID:24552285	PCS		9/24			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002716	PMID:26867732	PCS		4/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001945	PMID:24552285	PCS		13/24		HP:0031796	P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0012490	PMID:24552285	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002315	PMID:26867732	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002910	PMID:24552284	PCS		5/5			P	HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0200042	PMID:27059682;PMID:24552285	PCS		18/34			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001744	PMID:26867732;PMID:24552284	PCS		13/14			P	HPO:probinson[2020-11-28];HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0003326	PMID:24552285	PCS		11/24			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002633	PMID:27059682;PMID:26867732	PCS		7/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0004313	PMID:27059682	PCS		6/15			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0003621	PMID:26867732	PCS		2/9			C	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0005523	PMID:26867732	PCS		3/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001882	PMID:27444081;PMID:24552284	PCS		3/6			P	HPO:probinson[2020-11-28];HPO:skoehler[2014-04-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000155	PMID:27444081	PCS		1/1			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0030880	PMID:26867732;PMID:24552285	PCS		12/19			P	HPO:probinson[2020-11-28];HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0011108	PMID:27444081	PCS		1/1			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0011227	PMID:27444081	PCS		1/1			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0032154	PMID:26867732;PMID:24552285	PCS		5/33			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000822	PMID:27059682	PCS		2/15			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0009830	PMID:24552285	PCS		3/24			P	HPO:skoehler[2014-04-13];HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001954	PMID:27444081;PMID:26867732	PCS		4/10			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0030053	PMID:26867732	PCS		4/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0000988	PMID:26867732	PCS		3/9			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001433	PMID:27444081	PCS		1/1			P	HPO:probinson[2020-11-28]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0001876	PMID:24552284	PCS		2/5			P	HP:probinson[2019-03-02]
OMIM:615688	Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome		HP:0002721	PMID:27059682	PCS		7/15			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-11-28]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0003577	PMID:26870132	PCS		1/1			C	HPO:probinson[2022-10-10];HPO:probinson[2024-03-08]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0003038	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0001773	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0001371	OMIM:200700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0003097	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:6000650	PMID:27326275	PCS					P	HPO:probinson[2024-04-03]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0005792	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0008873	PMID:9288098	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0003826	OMIM:200700	TAS					C	HPO:probinson[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0006498	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0001522	OMIM:200700	IEA					C	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:6001052	PMID:27577507	PCS					P	HPO:probinson[2024-12-14]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0001964	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0001249	PMID:26870132	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0009803	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0003022	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0001162	PMID:9288098	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0003086	PMID:26870132	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-08]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0011927	OMIM:200700	TAS					P	HPO:skoehler[2013-06-03]
OMIM:200700	Acromesomelic dysplasia 2A		HP:6000921	PMID:27577507	PCS					P	HPO:probinson[2024-08-03]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0008081	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0000007	PMID:9288098	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-10]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0005914	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0005736	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0002984	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:200700	Acromesomelic dysplasia 2A		HP:0006228	OMIM:200700	IEA					P	HPO:iea[2009-02-17]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001397	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0031956	PMID:27815843;PMID:21786366	PCS		4/5			P	HPO:probinson[2021-10-04];HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001993	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001970	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0011968	PMID:21786366	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001263	PMID:21786366	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0002151	PMID:21786366	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0002240	PMID:21786366	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0003593	PMID:21786366	PCS		4/4			C	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0002094	PMID:21786366	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0030948	PMID:27815843;PMID:21786366	PCS		3/5			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0032653	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0031962	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0031964	PMID:27815843;PMID:21786366	PCS		4/5			P	HPO:probinson[2021-10-04];HPO:probinson[2021-10-04];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0003819	PMID:21786366	PCS		2/4			C	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001508	PMID:21786366	PCS	HP:0003593	3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001639	PMID:21786366	PCS	HP:0003593	4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001639	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0000007	PMID:21786366	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001942	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0003348	PMID:21786366	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0003623	PMID:27815843	IEA		1/1			C	HPO:probinson[2021-10-04]
OMIM:614582	Combined oxidative phosphorylation deficiency 9		HP:0001655	PMID:27815843	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0001250	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000072	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000819	OMIM:598500	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0012332	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000639	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000407	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000924	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000618	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0001889	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0001427	OMIM:598500	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000007	OMIM:598500	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000648	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0001924	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000873	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0001873	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0001249	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0000126	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:598500	Wolfram syndrome, mitochondrial form		HP:0001875	OMIM:598500	IEA					P	HPO:iea[2009-02-17]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0001276	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0002245	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0003577	PMID:30359777;PMID:24986372	PCS		2/2			C	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0002188	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000365	PMID:15220921	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0004322	PMID:15220921	PCS		2/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000243	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0002021	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0045055	PMID:24986372	PCS		1/1			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000518	PMID:15220921	PCS		2/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0001508	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0002719	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0033134	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000519	PMID:24986372	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0012472	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000656	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0001888	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0009886	PMID:24986372	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0001249	PMID:15220921	PCS		3/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000670	PMID:15220921	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000992	PMID:15220921;PMID:24986372	PCS		4/4			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000695	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0002299	PMID:15220921;PMID:24986372	PCS		4/4			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0011968	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0001263	PMID:24986372	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0003261	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0008064	PMID:15220921;PMID:24986372	PCS		3/4			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0007431	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0008069	PMID:15220921	PCS		0/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000007	PMID:15220921	PCS					I	HPO:skoehler[2015-09-25];HPO:probinson[2020-07-21]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000601	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000568	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0007479	PMID:15220921	PCS	HP:0003577	1/3			P	HPO:skoehler[2015-09-25];HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0007479	PMID:24986372	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0001511	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0008689	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0000369	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:616395	Trichothiodystrophy 3, photosensitive		HP:0001875	PMID:30359777	PCS		1/1			P	HPO:probinson[2022-04-12]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0002069	PMID:24157691	PCS		1/4			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0000252	PMID:24157691;PMID:28235671	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-02];HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0000274	PMID:28235671	PCS		1/1			P	HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0000750	PMID:24157691	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0002384	PMID:24157691	PCS		2/4			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0001263	PMID:24157691;PMID:28235671	PCS		1/5			P	HPO:probinson[2022-10-02];HPO:skoehler[2018-10-08];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0001252	PMID:28235671	PCS		1/1			P	HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0012332	PMID:28235671	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0011171	PMID:24157691	PCS		1/4			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0011463	PMID:24157691	PCS		3/4			C	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0020221	PMID:24157691	PCS		1/4			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0007018	PMID:24157691	PCS		1/4			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0007359	PMID:28235671	PCS		1/1			P	HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0000006	PMID:24157691	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-02]
OMIM:617935	Epilepsy, familial focal, with variable foci 4		HP:0003623	PMID:24157691;PMID:28235671	PCS		2/5			C	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000486	PMID:35047857	PCS		4/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0002144	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000023	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0004322	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0002186	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0003593	PMID:35047857	PCS		7/7			C	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0001270	PMID:35047857	PCS		6/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0025161	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0500041	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0007380	PMID:35047857	PCS		2/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0009185	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0100704	PMID:35047857	PCS		2/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000718	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000519	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0020046	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000733	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000752	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0001642	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000577	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000252	PMID:35047857	PCS		6/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000750	PMID:35047857	PCS		7/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0002650	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0002475	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0100710	PMID:35047857	PCS		1/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0007018	PMID:35047857	PCS		2/7			P	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000006	PMID:35047857	PCS					I	HPO:probinson[2022-12-12]
OMIM:620141	Developmental delay, language impairment, and ocular abnormalities		HP:0000126	PMID:35047857	PCS					P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0002069	PMID:7887420	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0001250	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0005157	OMIM:204200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0002361	PMID:7887420	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000518	OMIM:204200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000618	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000739	OMIM:204200	TAS					P	HPO:probinson[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0001922	PMID:7887420	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0007663	PMID:7887420	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0003208	PMID:7887420	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000510	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0001249	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0003205	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000550	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0003621	PMID:7887420	PCS		1/1			C	HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0002059	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0001300	PMID:7887420	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0003463	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0001260	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0002074	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0002071	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000709	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000529	PMID:7887420	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000726	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000608	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0001317	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000546	PMID:7887420	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000007	PMID:7553855	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000648	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0002505	PMID:7887420	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0000501	OMIM:204200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:204200	Ceroid lipofuscinosis, neuronal, 3		HP:0001336	OMIM:204200	IEA					P	HPO:iea[2009-02-17]
OMIM:217095	Conotruncal heart malformations		HP:0100259	OMIM:217095	TAS					P	HPO:skoehler[2015-02-22]
OMIM:217095	Conotruncal heart malformations		HP:0001660	OMIM:217095	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217095	Conotruncal heart malformations		HP:0001674	OMIM:217095	TAS					P	HPO:skoehler[2015-02-22]
OMIM:217095	Conotruncal heart malformations		HP:0010055	OMIM:217095	TAS				HP:0012832	P	HPO:skoehler[2015-02-22]
OMIM:217095	Conotruncal heart malformations		HP:0001719	OMIM:217095	IEA					P	HPO:iea[2009-02-17]
OMIM:217095	Conotruncal heart malformations		HP:0001939	OMIM:217095	IEA					P	HPO:iea[2009-02-17]
OMIM:217095	Conotruncal heart malformations		HP:0001680	OMIM:217095	TAS					P	HPO:skoehler[2015-02-22]
OMIM:217095	Conotruncal heart malformations		HP:0001669	OMIM:217095	TAS					P	HPO:skoehler[2012-10-17]
OMIM:217095	Conotruncal heart malformations		HP:0000316	OMIM:217095	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:217095	Conotruncal heart malformations		HP:0000007	OMIM:217095	IEA					I	HPO:iea[2009-02-17]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0007759	OMIM:271310	IEA					P	HPO:iea[2009-02-17]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0012040	OMIM:271310	TAS					P	HPO:probinson[2022-07-01]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0001131	OMIM:271310	IEA					P	HPO:iea[2009-02-17]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0001141	OMIM:271310	IEA					P	HPO:iea[2009-02-17]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0001251	OMIM:271310	IEA					P	HPO:iea[2009-02-17]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0000007	OMIM:271310	IEA					I	HPO:iea[2009-02-17]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0002503	OMIM:271310	IEA					P	HPO:iea[2009-02-17]
OMIM:271310	Spinocerebellar degeneration and corneal dystrophy		HP:0001249	OMIM:271310	IEA					P	HPO:iea[2009-02-17]
OMIM:150400	Tooth agenesis, selective, 4		HP:0009804	OMIM:150400	IEA					P	HPO:skoehler[2015-12-30]
OMIM:150400	Tooth agenesis, selective, 4		HP:0002231	PMID:19559398	PCS		6/9			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0010764	PMID:19559398	PCS		4/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0045075	PMID:19559398	PCS		7/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0010765	PMID:19559398	PCS		3/11			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0008391	PMID:19559398	PCS		6/12			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0000958	PMID:19559398	PCS		7/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0006481	PMID:19559398	PCS		6/12			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0006342	OMIM:150400	IEA					P	HPO:iea[2009-02-17]
OMIM:150400	Tooth agenesis, selective, 4		HP:0002209	PMID:19559398	PCS		7/12			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0000613	PMID:19559398	PCS		3/11			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0000007	PMID:19559398	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0007410	PMID:19559398	PCS		3/11			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0000966	PMID:19559398	PCS		3/11			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0000006	PMID:19559398	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0000963	PMID:19559398	PCS		3/11			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0001810	PMID:19559398	PCS		8/12			P	HPO:probinson[2022-10-01]
OMIM:150400	Tooth agenesis, selective, 4		HP:0006349	PMID:19559398	PCS		12/12			P	HPO:probinson[2022-10-01]
OMIM:222748	Dihydropyrimidinuria		HP:0001254	OMIM:222748	IEA					P	HPO:iea[2009-02-17]
OMIM:222748	Dihydropyrimidinuria		HP:0003654	PMID:17383919	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:222748	Dihydropyrimidinuria		HP:0003236	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:222748	Dihydropyrimidinuria		HP:0002023	OMIM:222748	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222748	Dihydropyrimidinuria		HP:0001250	PMID:20362666	PCS		6/20			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:6000331	PMID:20362666	PCS					P	HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:6000211	PMID:6467612	PCS		1/1			P	HPO:probinson[2024-02-09]
OMIM:222748	Dihydropyrimidinuria		HP:6000118	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:222748	Dihydropyrimidinuria		HP:0002062	OMIM:222748	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222748	Dihydropyrimidinuria		HP:4000095	PMID:17383919	PCS		2/2			P	HPO:probinson[2023-01-27]
OMIM:222748	Dihydropyrimidinuria		HP:0012544	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:222748	Dihydropyrimidinuria		HP:0012127	PMID:17383919	PCS		2/2			P	HPO:probinson[2022-12-13]
OMIM:222748	Dihydropyrimidinuria		HP:6000119	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:222748	Dihydropyrimidinuria		HP:0031964	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:222748	Dihydropyrimidinuria		HP:0001508	PMID:20362666	PCS		4/20			P	HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:0000717	PMID:20362666	PCS		3/20			P	HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:6000083	OMIM:222748	TAS					P	HPO:probinson[2024-01-06]
OMIM:222748	Dihydropyrimidinuria		HP:0000752	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:222748	Dihydropyrimidinuria		HP:0009803	OMIM:222748	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222748	Dihydropyrimidinuria		HP:0001942	OMIM:222748	IEA					P	HPO:iea[2009-02-17]
OMIM:222748	Dihydropyrimidinuria		HP:0001249	PMID:20362666	PCS		12/19			P	HPO:skoehler[2013-06-16];HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:0007308	OMIM:222748	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222748	Dihydropyrimidinuria		HP:0031956	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:222748	Dihydropyrimidinuria		HP:0000252	PMID:20362666	PCS		3/20			P	HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:0001762	OMIM:222748	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222748	Dihydropyrimidinuria		HP:0000750	PMID:17383919	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-13]
OMIM:222748	Dihydropyrimidinuria		HP:0011968	PMID:20362666	PCS		7/20			P	HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:0001262	OMIM:222748	IEA					P	HPO:iea[2009-02-17]
OMIM:222748	Dihydropyrimidinuria		HP:0033139	PMID:17383919	PCS		1/2			P	HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:222748	Dihydropyrimidinuria		HP:0034593	OMIM:222748	TAS					P	HPO:probinson[2023-03-31]
OMIM:222748	Dihydropyrimidinuria		HP:0000007	PMID:17383919	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:222748	Dihydropyrimidinuria		HP:0007256	OMIM:222748	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:222748	Dihydropyrimidinuria		HP:0001357	OMIM:222748	IEA					P	HPO:skoehler[2010-06-20]
OMIM:222748	Dihydropyrimidinuria		HP:0001510	PMID:20362666	PCS		4/20			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-02-27]
OMIM:222748	Dihydropyrimidinuria		HP:0003710	PMID:30384990	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:222748	Dihydropyrimidinuria		HP:0002500	OMIM:222748	IEA					P	HPO:skoehler[2010-06-20]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0002015	PMID:31332380	PCS		4/6			P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0002059	PMID:31332380	PCS					P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0001260	PMID:31332380	PCS		6/6			P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0003581	PMID:31332380	PCS					C	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0002460	PMID:31332380	PCS		4/4			P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0001251	PMID:31332380	PCS		1/4		HP:0012825	P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0030319	PMID:31332380	PCS		4/4			P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0000508	PMID:31332380	PCS		6/6			P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0002878	PMID:31332380	PCS	HP:0003584	2/4			P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0003701	PMID:31332380	PCS		4/4			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0002579	PMID:31332380	PCS					P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0000006	PMID:31332380	PCS					I	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0001337	PMID:31332380	PCS		1/4			P	HPO:probinson[2020-07-14]
OMIM:618637	Oculopharyngeal myopathy with leukoencephalopathy 1		HP:0000544	PMID:31332380	PCS		3/4			P	HPO:probinson[2020-07-14]
OMIM:238710	Hyperlysinemia due to defect in lysine transport into mitochondria		HP:0008265	OMIM:238710	IEA					P	HPO:iea[2009-02-17]
OMIM:238710	Hyperlysinemia due to defect in lysine transport into mitochondria		HP:0000007	OMIM:238710	IEA					I	HPO:iea[2009-02-17]
OMIM:238710	Hyperlysinemia due to defect in lysine transport into mitochondria		HP:0002161	OMIM:238710	IEA					P	HPO:iea[2009-02-17]
OMIM:238710	Hyperlysinemia due to defect in lysine transport into mitochondria		HP:0001249	OMIM:238710	IEA					P	HPO:iea[2009-02-17]
OMIM:613762	46,xy sex reversal 6		HP:0100621	PMID:21129722	PCS		1/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:613762	46,xy sex reversal 6		HP:0012245	PMID:21129722	PCS		12/17			P	HPO:probinson[2013-04-02];HPO:probinson[2022-12-13]
OMIM:613762	46,xy sex reversal 6		HP:0000133	PMID:21129722	PCS		13/13			P	HPO:probinson[2022-12-13]
OMIM:613762	46,xy sex reversal 6		HP:0000150	PMID:21129722	PCS		1/17			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:613762	46,xy sex reversal 6		HP:0000041	OMIM:613762	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613762	46,xy sex reversal 6		HP:0008665	PMID:21129722	PCS		1/17			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-12-13]
OMIM:613762	46,xy sex reversal 6		HP:0000047	PMID:21129722	PCS		4/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:613762	46,xy sex reversal 6		HP:0000006	PMID:21129722	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-13]
OMIM:613762	46,xy sex reversal 6		HP:0001007	OMIM:613762	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613762	46,xy sex reversal 6		HP:0002215	OMIM:613762	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000286	PMID:19617690	PCS		2/4			P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002421	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002188	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001773	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000486	PMID:19617690	PCS		1/4			P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001252	PMID:19617690	PCS		3/4			P	HPO:skoehler[2014-11-26]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0010055	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000238	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001847	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0009623	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002414	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0020049	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001249	PMID:19617690	PCS		2/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000358	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0003700	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002553	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000494	PMID:19617690	PCS		1/4			P	HPO:skoehler[2012-11-20]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001385	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000252	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001344	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000331	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0011968	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001382	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001263	PMID:19617690	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000294	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0012736	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001182	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0011448	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0006380	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002506	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001537	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002705	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002987	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000960	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000322	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000006	PMID:19617690	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000248	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000324	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0006801	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000341	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0003577	PMID:19617690	PCS		4/4			C	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000463	PMID:19617690	PCS		1/4			P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000262	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0040158	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000414	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001822	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000218	PMID:19617690	PCS		1/4			P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001466	PMID:19617690	PCS					I	HPO:skoehler[2013-01-22];HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001166	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001562	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000475	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0002650	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0004279	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000232	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000034	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000276	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0003186	OMIM:613776	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000470	PMID:19617690	PCS		1/4			P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0045025	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0005280	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000506	PMID:19617690	PCS		2/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000508	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000426	PMID:19617690	PCS		1/4			P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001558	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000348	OMIM:613776	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0001357	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000664	PMID:19617690	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:613776	Chromosome 17p13.1 deletion syndrome		HP:0000465	OMIM:613776	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614019	Lissencephaly 4		HP:0001276	PMID:21529751	PCS		2/3			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0003577	PMID:21529752;PMID:21529751	PCS		10/10			C	HPO:probinson[2022-08-07];HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0000431	PMID:21529751	PCS		4/4			P	HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0004322	PMID:21529752;PMID:21529751	PCS		4/10			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0030048	PMID:21529751	PCS		1/3			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0001321	PMID:21529752;PMID:21529751	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0003487	PMID:21529751	PCS		1/3			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0001250	PMID:21529752;PMID:21529751	PCS		7/9			P	HPO:skoehler[2012-11-28];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0011968	PMID:21529752	PCS		6/6			P	HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0001263	PMID:21529752;PMID:21529751	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0001274	PMID:21529752;PMID:21529751	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0011451	PMID:21529752;PMID:21529751	PCS	HP:0003577	10/10		HP:0012828;HP:0012828	P	HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0001339	PMID:21529752;PMID:21529751	PCS		2/4			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0000007	PMID:21529752	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0001510	PMID:21529751	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0009879	PMID:21529752;PMID:21529751	PCS		5/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:614019	Lissencephaly 4		HP:0001347	PMID:21529751	PCS		1/3			P	HPO:probinson[2022-08-07];HPO:probinson[2022-08-07]
OMIM:267200	Renal tubular acidosis III		HP:0000121	OMIM:267200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:267200	Renal tubular acidosis III		HP:0002748	OMIM:267200	IEA					P	HPO:iea[2009-02-17]
OMIM:267200	Renal tubular acidosis III		HP:0000007	OMIM:267200	IEA					I	HPO:iea[2009-02-17]
OMIM:267200	Renal tubular acidosis III		HP:0002749	OMIM:267200	IEA					P	HPO:iea[2009-02-17]
OMIM:267200	Renal tubular acidosis III		HP:0002900	OMIM:267200	IEA					P	HPO:iea[2009-02-17]
OMIM:267200	Renal tubular acidosis III		HP:0003768	OMIM:267200	IEA					P	HPO:iea[2009-02-17]
OMIM:267200	Renal tubular acidosis III		HP:0000787	OMIM:267200	IEA					P	HPO:iea[2009-02-17]
OMIM:267200	Renal tubular acidosis III		HP:0004910	OMIM:267200	IEA					P	HPO:iea[2009-02-17]
OMIM:146510	Pallister-Hall syndrome		HP:0001177	PMID:24736735	PCS		0/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0001770	PMID:24736735	PCS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0002023	PMID:24736735	PCS		9/20			P	HPO:probinson[2012-04-24];HPO:probinson[2024-03-23]
OMIM:146510	Pallister-Hall syndrome		HP:0004322	OMIM:146510	TAS					P	HPO:skoehler[2014-06-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000089	PMID:26604140	PCS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0002101	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0001250	PMID:24736735	PCS					P	HPO:probinson[2009-10-16]
OMIM:146510	Pallister-Hall syndrome		HP:0003196	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000086	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2017-05-28]
OMIM:146510	Pallister-Hall syndrome		HP:0010564	PMID:15782417;PMID:24736735	PCS		13/18			P	HPO:probinson[2012-06-10];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0010567	PMID:24736735	PCS		14/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0003828	OMIM:146510	TAS					M	HPO:skoehler[2015-12-30]
OMIM:146510	Pallister-Hall syndrome		HP:0002937	OMIM:146510	TAS		HP:0040284			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000835	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0001841	PMID:24736735	PCS		0/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0001643	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0006159	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0008734	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0007601	OMIM:146510	TAS		HP:0040284			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000358	OMIM:146510	TAS		HP:0040284			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0001249	PMID:24736735	PCS		3/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0006118	PMID:24736735	PCS		12/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0003048	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000054	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000175	PMID:24736735	PCS		3/21			P	HPO:probinson[2021-02-21]
OMIM:146510	Pallister-Hall syndrome		HP:0000695	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000453	PMID:24736735	PCS		3/21			P	HPO:probinson[2021-02-21]
OMIM:146510	Pallister-Hall syndrome		HP:0000171	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0001263	PMID:24736735	PCS		3/14			P	HPO:probinson[2017-05-28]
OMIM:146510	Pallister-Hall syndrome		HP:0010112	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0100259	PMID:24736735	PCS		17/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0008163	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0100258	PMID:20301638	PCS		0/21			P	HPO:probinson[2017-05-28];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0010044	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0002827	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000568	OMIM:146510	TAS		HP:0040284			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000204	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000006	PMID:24736735	PCS					I	HPO:probinson[2012-04-24];HPO:probinson[2021-02-21]
OMIM:146510	Pallister-Hall syndrome		HP:0000126	PMID:26604140	PCS					P	HPO:probinson[2017-05-28]
OMIM:146510	Pallister-Hall syndrome		HP:0002444	PMID:24736735	PCS		11/11			P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-23]
OMIM:146510	Pallister-Hall syndrome		HP:0003577	PMID:24736735	PCS		20/20			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0008706	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0000463	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0002164	PMID:24736735	PCS		8/12			P	HPO:probinson[2012-04-24];HPO:probinson[2024-03-23]
OMIM:146510	Pallister-Hall syndrome		HP:0005151	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0001629	PMID:24736735	PCS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0008551	OMIM:146510	TAS		HP:0040284			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0008751	OMIM:146510	TAS		HP:0040282			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000413	OMIM:146510	TAS		HP:0040284			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0005349	PMID:15782417	PCS					P	HPO:probinson[2012-06-10]
OMIM:146510	Pallister-Hall syndrome		HP:0001545	PMID:24736735	PCS		1/21			P	HPO:probinson[2021-02-21]
OMIM:146510	Pallister-Hall syndrome		HP:0000110	PMID:26604140	PCS					P	HPO:skoehler[2012-10-17]
OMIM:146510	Pallister-Hall syndrome		HP:0003027	PMID:24736735	PCS		4/21			P	HPO:probinson[2017-05-28]
OMIM:146510	Pallister-Hall syndrome		HP:0000871	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0001162	PMID:24736735	PCS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0001360	OMIM:146510	TAS					P	HPO:skoehler[2012-10-17]
OMIM:146510	Pallister-Hall syndrome		HP:0000072	PMID:26604140	PCS					P	HPO:probinson[2017-05-28]
OMIM:146510	Pallister-Hall syndrome		HP:0005280	OMIM:146510	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0012165	PMID:24736735	PCS		3/21			P	HPO:skoehler[2013-02-25]
OMIM:146510	Pallister-Hall syndrome		HP:0000826	PMID:20301638	PCS					P	HPO:probinson[2009-10-16]
OMIM:146510	Pallister-Hall syndrome		HP:0006042	PMID:24736735	PCS		14/17			P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-23]
OMIM:146510	Pallister-Hall syndrome		HP:0000902	OMIM:146510	TAS		HP:0040284			P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0008188	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000107	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0000824	PMID:20301638	PCS					P	HPO:probinson[2009-10-16];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0001159	PMID:24736735	PCS		8/21			P	HPO:probinson[2021-02-21]
OMIM:146510	Pallister-Hall syndrome		HP:0001830	PMID:24736735	PCS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0003811	PMID:20301638	PCS					C	HPO:probinson[2012-04-24];HPO:probinson[2024-03-08]
OMIM:146510	Pallister-Hall syndrome		HP:0001511	OMIM:146510	TAS					P	HPO:skoehler[2012-10-17]
OMIM:146510	Pallister-Hall syndrome		HP:0001510	PMID:24736735	PCS		10/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:146510	Pallister-Hall syndrome		HP:0006402	OMIM:146510	TAS					P	HPO:probinson[2012-04-24]
OMIM:146510	Pallister-Hall syndrome		HP:0000028	OMIM:146510	TAS					P	HPO:skoehler[2014-06-24]
OMIM:618145	Deafness, autosomal recessive 111		HP:0003621	PMID:29961571	PCS					C	HPO:probinson[2022-11-08]
OMIM:618145	Deafness, autosomal recessive 111		HP:0000408	PMID:29961571	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-08]
OMIM:618145	Deafness, autosomal recessive 111		HP:0011463	PMID:29961571	PCS					C	HPO:probinson[2022-11-08]
OMIM:618145	Deafness, autosomal recessive 111		HP:0000007	PMID:29961571	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-08]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0002521	PMID:27889060	PCS		3/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0003577	PMID:27889060	PCS		3/9			C	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0001272	PMID:27889060	PCS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0001250	PMID:27889060	PCS		8/8		HP:0031375	P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0003593	PMID:27889060	PCS		5/9			C	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0001290	PMID:27889060	PCS		7/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000817	PMID:27889060	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000637	PMID:27889060	PCS		1/12			P	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0025336	PMID:27889060	PCS		11/11			P	HPO:probinson[2021-02-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000510	PMID:27889060	PCS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0003623	PMID:27889060	PCS		1/9			C	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0008936	PMID:27889060	PCS		12/12			P	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0001265	PMID:27889060	PCS		8/11			P	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000252	PMID:27889060	PCS		9/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0002059	PMID:27889060	PCS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0001344	PMID:27889060	PCS		4/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0002133	PMID:27889060	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0002079	PMID:27889060	PCS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0031936	PMID:27889060	PCS		11/11			P	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0001263	PMID:27889060	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0100660	PMID:27889060	PCS		5/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0002509	PMID:27889060	PCS		4/12			P	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000007	PMID:27889060	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0200134	PMID:27889060	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000527	PMID:27889060	PCS		1/12			P	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000543	PMID:27889060	PCS		4/11			P	HPO:probinson[2021-02-13]
OMIM:617276	Developmental and epileptic encephalopathy 48		HP:0000520	PMID:27889060	PCS		2/12			P	HPO:probinson[2021-02-13]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0002223	OMIM:263700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0003577	PMID:2331520	PCS		2/2			C	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0001596	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0004322	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0001010	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0002240	PMID:2331520	PCS		2/2			P	HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0011457	OMIM:263700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:6000514	PMID:3674403	PCS					P	HPO:probinson[2024-04-03]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0001072	OMIM:263700	TAS					P	HPO:probinson[2012-05-06]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0033009	PMID:2331520	PCS		2/2			P	HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0030756	OMIM:263700	TAS		20/20			P	HPO:probinson[2022-12-21];HPO:probinson[2022-12-21];HPO:skoehler[2019-09-07]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0100324	OMIM:263700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000938	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0032001	OMIM:263700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000998	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000953	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000559	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0002953	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0002756	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0002797	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0001744	PMID:2331520	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000952	PMID:2331520	PCS		2/2			P	HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0040318	PMID:2331520	PCS		2/2			P	HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000992	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0034905	OMIM:263700	TAS					P	HPO:probinson[2023-07-18]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0001081	OMIM:263700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0009473	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000509	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000987	OMIM:263700	IEA					P	HPO:iea[2009-02-17]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0001878	PMID:2331520	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0000007	PMID:2331520	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:263700	Porphyria, congenital erythropoietic		HP:0001873	PMID:2331520	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:601414	Retinitis pigmentosa 18		HP:0000662	OMIM:601414	IEA					P	HPO:iea[2009-02-17]
OMIM:601414	Retinitis pigmentosa 18		HP:0008043	OMIM:601414	IEA					P	HPO:iea[2009-02-17]
OMIM:601414	Retinitis pigmentosa 18		HP:0000510	OMIM:601414	TAS					P	HPO:skoehler[2015-01-21]
OMIM:601414	Retinitis pigmentosa 18		HP:0000575	OMIM:601414	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601414	Retinitis pigmentosa 18		HP:0000006	OMIM:601414	IEA					I	HPO:iea[2009-02-17]
OMIM:601414	Retinitis pigmentosa 18		HP:0007987	OMIM:601414	IEA					P	HPO:iea[2009-02-17]
OMIM:609048	Melanoma, cutaneous malignant, susceptibility to, 3		HP:0012056	OMIM:609048	TAS					P	HPO:probinson[2012-08-01]
OMIM:609048	Melanoma, cutaneous malignant, susceptibility to, 3		HP:0001074	OMIM:609048	TAS					P	HPO:probinson[2009-02-17]
OMIM:609048	Melanoma, cutaneous malignant, susceptibility to, 3		HP:0001062	OMIM:609048	TAS					P	HPO:probinson[2009-02-17]
OMIM:609048	Melanoma, cutaneous malignant, susceptibility to, 3		HP:0001054	OMIM:609048	TAS					P	HPO:probinson[2009-02-17]
OMIM:609048	Melanoma, cutaneous malignant, susceptibility to, 3		HP:0000006	OMIM:609048	TAS					I	HPO:probinson[2009-02-17]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002421	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001310	PMID:24777941	PCS		1/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001332	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001251	PMID:24777941	PCS		2/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0003593	PMID:24777941	PCS		4/4			C	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002061	PMID:24777941	PCS		3/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001270	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002080	PMID:24777941	PCS		1/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0000639	PMID:24777941	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0007024	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002415	PMID:24777941	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001347	PMID:24777941	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0008936	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0000252	PMID:24777941	PCS		1/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001583	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002059	PMID:24777941	PCS		2/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0003487	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002079	PMID:24777941	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0011968	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002395	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001260	PMID:24777941	PCS		1/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0001263	PMID:24777941	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0002071	OMIM:616140	TAS					P	HPO:skoehler[2015-01-04]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0012043	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0007179	PMID:24777941	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:616140	Leukodystrophy, hypomyelinating, 9		HP:0000007	PMID:24777941	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-23]
OMIM:619273	Cimdag syndrome		HP:0030854	PMID:33186545	PCS		1/3			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001332	PMID:33186545	PCS		5/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001250	PMID:33186545	PCS		3/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001252	PMID:33186545	PCS		5/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001251	PMID:33186545	PCS		2/4			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0002240	PMID:33186545	PCS		4/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001270	PMID:33186545	PCS		5/5			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0033725	PMID:33186545	PCS		2/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0002719	PMID:33186545	PCS		1/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000519	PMID:33186545	PCS		4/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0009125	PMID:33186545	PCS		1/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000135	PMID:33186545	PCS		1/4			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000556	PMID:33186545	PCS		3/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001320	PMID:33186545	PCS		1/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0002059	PMID:33186545	PCS		1/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0006879	PMID:33186545	PCS		1/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000252	PMID:33186545	PCS		6/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001344	PMID:33186545	PCS		2/5			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000750	PMID:33186545	PCS		5/5			P	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001321	PMID:33186545	PCS		2/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0011968	PMID:33186545	PCS		4/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0002072	PMID:33186545	PCS		1/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001081	PMID:33186545	PCS		1/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0011344	PMID:33186545	PCS		6/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000407	PMID:33186545	PCS		2/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0100613	PMID:33186545	PCS		2/6			C	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0011451	PMID:33186545	PCS		3/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0025405	PMID:33186545	PCS		3/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000505	PMID:33186545	PCS		6/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001257	PMID:33186545	PCS		4/5			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0000006	PMID:33186545	PCS					I	HPO:probinson[2021-06-19];HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0002126	PMID:33186545	PCS		1/6			P	HPO:probinson[2021-06-19]
OMIM:619273	Cimdag syndrome		HP:0001414	PMID:33186545	PCS		1/5			P	HPO:probinson[2021-06-19]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002015	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0003487	PMID:19122027	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0000980	OMIM:606353	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002464	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002120	OMIM:606353	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0000183	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0001285	PMID:19122027	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0001152	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002064	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002193	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002491	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0033383	PMID:19122027	PCS		1/3			P	HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0034353	PMID:19122027	PCS		3/3			P	HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0011463	PMID:19122027	PCS		3/3			C	HPO:probinson[2013-12-15];HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0007024	PMID:19122027	PCS		3/3			P	HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0000007	PMID:11586298	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002505	PMID:19122027	PCS		2/3			P	HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0003677	OMIM:606353	IEA					C	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002127	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0001347	PMID:19122027	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0002501	OMIM:606353	IEA					P	HPO:iea[2009-02-17]
OMIM:606353	Primary lateral sclerosis, juvenile		HP:0025747	OMIM:606353	TAS					P	HPO:probinson[2024-08-04]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001276	PMID:15537906	PCS		2/2			P	HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001396	PMID:15537906	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0003577	PMID:15537906	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001250	OMIM:609060	TAS				HP:0031375	P	HPO:skoehler[2013-06-06]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0002283	PMID:15537906	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0002240	OMIM:609060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0012448	OMIM:609060	TAS					P	HPO:skoehler[2013-11-28]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001270	OMIM:609060	IEA					P	HPO:iea[2009-02-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0032653	PMID:15537906	IEA		2/2			P	HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0000639	OMIM:609060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0000817	OMIM:609060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001942	PMID:15537906	PCS		2/2		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0006799	PMID:15537906	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001347	OMIM:609060	TAS					P	HPO:probinson[2012-09-10]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0008936	OMIM:609060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0000252	PMID:15537906	PCS		1/2		HP:0012825	P	HPO:probinson[2012-04-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0002375	PMID:15537906	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0002079	PMID:15537906	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0011968	OMIM:609060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0011924	PMID:15537906	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0011925	PMID:15537906	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0002151	PMID:15537906	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0002490	OMIM:609060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0011923	PMID:15537906	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0000007	PMID:15537906	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0008347	PMID:15537906	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001511	PMID:15537906	PCS	HP:0011461	1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0001257	OMIM:609060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609060	Combined oxidative phosphorylation deficiency 1		HP:0004448	PMID:15537906	PCS	HP:0003623	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-12]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0010627	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0004322	PMID:16968807	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000463	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0003196	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0001252	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0003593	PMID:16968807	PCS		1/1			C	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0001508	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0011220	OMIM:613038	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0001609	PMID:1302000	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0031098	PMID:16968807;PMID:1302000	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0033078	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0011120	PMID:1302000	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0008850	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000158	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0006579	OMIM:613038	TAS					P	HPO:skoehler[2013-06-03]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000952	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0001249	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0011968	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000270	OMIM:613038	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000490	OMIM:613038	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0200028	PMID:1302000	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000272	OMIM:613038	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0034323	PMID:16968807;PMID:1302000	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0011800	OMIM:613038	TAS					P	HPO:skoehler[2013-11-28]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0031079	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0040075	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0005280	OMIM:613038	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0032210	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0008202	PMID:16968807;PMID:1302000	PCS		2/2			P	HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000821	PMID:16968807	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000007	OMIM:613038	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0002007	OMIM:613038	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0000006	PMID:1302000	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:613038	Pituitary hormone deficiency, combined, 1		HP:0033082	PMID:16968807	PCS		1/1			P	HPO:probinson[2022-09-26]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0004322	PMID:18728160	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0001250	PMID:18728160	PCS		1/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0011968	PMID:18728160	PCS		1/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0030344	PMID:18728160	PCS		1/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0030341	PMID:18728160	PCS		1/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0011755	PMID:18728160	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0034323	PMID:18728160	PCS		2/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0011757	PMID:18728160	PCS		1/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0002904	PMID:18728160	PCS		1/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0031098	PMID:18728160	PCS		2/2			P	HPO:probinson[2022-12-02];HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0001998	PMID:18728160	PCS		2/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0001943	PMID:18728160	PCS		1/2			P	HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0002920	PMID:18728160	PCS		2/2			P	HPO:probinson[2022-12-02];HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0000006	PMID:18728160	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-02]
OMIM:613986	Pituitary hormone deficiency, combined, 6		HP:0003623	PMID:18728160	PCS		2/2			C	HPO:probinson[2022-12-02]
OMIM:609706	Deafness, autosomal recessive 53		HP:0000407	OMIM:609706	TAS					P	HPO:probinson[2013-03-30]
OMIM:609706	Deafness, autosomal recessive 53		HP:0000007	OMIM:609706	TAS					I	HPO:probinson[2013-01-09]
OMIM:619515	Spermatogenic failure 56		HP:0033393	PMID:34237282	PCS		5/5			P	HPO:probinson[2021-09-04]
OMIM:619515	Spermatogenic failure 56		HP:0032560	PMID:34237282	PCS		5/5			P	HPO:probinson[2021-09-04]
OMIM:619515	Spermatogenic failure 56		HP:0034011	PMID:34237282	PCS		5/5			P	HPO:probinson[2021-10-03]
OMIM:619515	Spermatogenic failure 56		HP:0003251	PMID:34237282	PCS		5/5			P	HPO:probinson[2021-09-04]
OMIM:619515	Spermatogenic failure 56		HP:0000007	PMID:34237282	PCS					I	HPO:probinson[2021-09-04];HPO:probinson[2021-09-04]
OMIM:619515	Spermatogenic failure 56		HP:0012207	PMID:34237282	PCS		5/5			P	HPO:probinson[2021-09-04]
OMIM:619515	Spermatogenic failure 56		HP:0000798	PMID:34237282	PCS		3/5			P	HPO:probinson[2021-09-04]
OMIM:619515	Spermatogenic failure 56		HP:0032558	PMID:34237282	PCS		4/5			P	HPO:probinson[2021-09-04]
OMIM:619515	Spermatogenic failure 56		HP:0032559	PMID:34237282	PCS		5/5			P	HPO:probinson[2021-09-04]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000164	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0006989	PMID:24241535	PCS		1/5			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0004322	OMIM:151050	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001252	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000041	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001290	OMIM:151050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0004482	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0006152	PMID:24241535	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000916	PMID:24241535	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0011220	PMID:24241535	PCS		5/5			P	HPO:skoehler[2013-08-11];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0002937	PMID:24241535	PCS		1/5			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000316	PMID:24241535	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000239	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0003745	OMIM:151050	IEA					I	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001249	PMID:24241535	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001187	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000252	PMID:24241535	PCS		3/5			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000175	PMID:24241535	PCS		1/5			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000453	PMID:24241535	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000452	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0002750	PMID:24241535	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001382	PMID:24241535	PCS		5/5			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000171	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0003041	PMID:24241535	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0010554	PMID:24241535	PCS		5/5			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0006380	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000407	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000965	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000400	PMID:24241535;OMIM:151050	PCS		15/15			P	HPO:probinson[2013-08-07];HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0002987	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000047	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0007678	PMID:24241535	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000006	PMID:24241535	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000963	OMIM:151050	TAS					P	HPO:probinson[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000885	PMID:24241535;OMIM:151050	PCS		15/15			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0005019	PMID:24241535	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0003015	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0010627	PMID:24241535	PCS		2/3			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000023	PMID:24241535	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0005477	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0002120	PMID:24241535	PCS		2/3			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0003298	PMID:24241535	PCS		1/5			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001274	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0008070	PMID:24241535	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001508	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0006297	PMID:24241535	PCS		4/4			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000337	PMID:24241535	PCS		5/5			P	HPO:skoehler[2013-08-11];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0009843	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0002119	PMID:24241535	PCS		2/3			P	HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001545	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000973	PMID:24241535	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000270	PMID:24241535	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001043	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0002007	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001511	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0001159	OMIM:151050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000028	PMID:24241535	PCS		2/2	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000347	OMIM:151050	IEA					P	HPO:iea[2009-02-17]
OMIM:151050	Lenz-Majewski hyperostotic dwarfism		HP:0000303	PMID:24241535	PCS		5/5			P	HPO:probinson[2023-02-12]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0002465	PMID:26463574	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0000252	PMID:26463574;PMID:24781755	PCS		8/9			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0002079	PMID:24781755	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0004322	PMID:26463574;PMID:24781755	PCS		7/9			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0001250	PMID:26463574;PMID:24781755	PCS		9/9			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0002110	PMID:26463574	PCS		1/4			P	HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0001252	PMID:26463574	PCS		1/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0001263	PMID:24781755	PCS		5/5			P	HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0003593	PMID:26463574;PMID:24781755	PCS		8/9			C	HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0100704	PMID:24781755	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0000007	PMID:24781755	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0000648	PMID:26463574	PCS		3/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0001510	PMID:24781755	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2023-06-04]
OMIM:616632	Seizures, cortical blindness, and microcephaly syndrome		HP:0003623	PMID:26463574	PCS		1/4			C	HPO:probinson[2023-06-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0001188	PMID:28934391	PCS	HP:0011461	2/3			P	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0003049	PMID:28934391	PCS	HP:0011461	1/3			P	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0001762	PMID:28934391	PCS	HP:0011461	1/3			P	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0001321	PMID:28934391	PCS	HP:0011461	2/3			P	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0001274	PMID:28934391	PCS	HP:0011461	1/3			P	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0011461	PMID:28934391	PCS		4/4			C	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0000007	PMID:28934391	PCS					I	HPO:probinson[2021-09-04];HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0002804	PMID:28934391	PCS	HP:0011461	3/3			P	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0002119	PMID:28934391	PCS	HP:0011461	4/4			P	HPO:probinson[2021-09-04]
OMIM:619501	Ventriculomegaly and arthrogryposis		HP:0000347	PMID:28934391	PCS	HP:0011461	1/3			P	HPO:probinson[2021-09-04]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0003236	PMID:17103435	PCS		0/7			P	HPO:probinson[2013-12-21];HPO:probinson[2024-03-08]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0001883	PMID:17103435	PCS		0/7			P	HPO:probinson[2024-03-08]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0003089	OMIM:187370	TAS					P	HPO:probinson[2009-02-17]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0100490	OMIM:187370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0005684	PMID:17103435	PCS		7/7			P	HPO:probinson[2013-12-21];HPO:probinson[2024-03-08]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0011463	PMID:17103435	PCS		7/7			C	HPO:probinson[2013-12-21];HPO:probinson[2024-03-08]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0008112	OMIM:187370;PMID:17103435	PCS		17/17			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0001239	OMIM:187370	TAS					P	HPO:probinson[2009-02-17]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0030051	PMID:17103435	PCS		7/7			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0002987	OMIM:187370	TAS					P	HPO:probinson[2009-02-17]
OMIM:187370	Arthrogryposis, distal, type 10		HP:0000006	PMID:17103435	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-08]
OMIM:614025	Hepatic lipase deficiency		HP:0002155	PMID:22798447;PMID:6961921	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:614025	Hepatic lipase deficiency		HP:0001013	PMID:22798447;PMID:6961921	PCS		1/3			P	HPO:probinson[2021-07-08];HPO:skoehler[2012-10-17];HPO:probinson[2021-07-08]
OMIM:614025	Hepatic lipase deficiency		HP:0003124	PMID:22798447;PMID:6961921	PCS		3/3			P	HPO:probinson[2021-07-08]
OMIM:614025	Hepatic lipase deficiency		HP:0012184	PMID:22798447	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:614025	Hepatic lipase deficiency		HP:0001084	PMID:6961921	PCS		1/2			P	HPO:probinson[2021-07-08]
OMIM:614025	Hepatic lipase deficiency		HP:0001681	PMID:6961921	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-08]
OMIM:614025	Hepatic lipase deficiency		HP:0000007	PMID:1671786	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-08]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001058	OMIM:219090	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0004586	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0003154	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0031364	OMIM:219090	IEA					P	HPO:skoehler[2018-10-08]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0012743	OMIM:219090	TAS					P	HPO:skoehler[2015-01-20]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000939	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001948	OMIM:219090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000979	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000712	OMIM:219090	TAS					P	HPO:skoehler[2015-10-05]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000876	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000978	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0002953	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001345	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001007	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0003202	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0002893	OMIM:219090	IEA					P	HPO:skoehler[2015-01-27]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001041	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001065	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0040270	OMIM:219090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0100852	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000969	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0002808	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000822	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000007	OMIM:219090	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0002900	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000787	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000963	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001513	OMIM:219090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0000006	OMIM:219090	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:219090	Pituitary adenoma 4, ACTH-secreting, somatic		HP:0001952	OMIM:219090	IEA					P	HPO:iea[2009-02-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0001909	OMIM:614743	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0001915	OMIM:614743	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0003581	OMIM:614743	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0003829	OMIM:614743	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0001394	OMIM:614743	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0005528	OMIM:614743	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0002216	OMIM:614743	TAS					P	HPO:skoehler[2013-06-03]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0002206	OMIM:614743	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0012324	OMIM:614743	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0001876	OMIM:614743	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614743	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 2		HP:0000006	OMIM:614743	TAS					I	HPO:skoehler[2012-10-17]
OMIM:618179	Microcephaly 24, primary, autosomal recessive		HP:0001320	PMID:30179222	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:618179	Microcephaly 24, primary, autosomal recessive		HP:0003577	PMID:30179222	PCS		3/3			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-18]
OMIM:618179	Microcephaly 24, primary, autosomal recessive		HP:0011451	PMID:30179222	PCS		3/3			P	HPO:probinson[2023-02-18]
OMIM:618179	Microcephaly 24, primary, autosomal recessive		HP:0000007	PMID:30179222	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618179	Microcephaly 24, primary, autosomal recessive		HP:0004209	PMID:30179222	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618179	Microcephaly 24, primary, autosomal recessive		HP:0001249	PMID:30179222	PCS		3/3			P	HPO:probinson[2023-02-18]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0003202	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0000123	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0001250	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0000407	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0001251	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0001350	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0000007	OMIM:274240	IEA					I	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0001873	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0000853	OMIM:274240	IEA					P	HPO:skoehler[2010-06-20]
OMIM:274240	Thyrocerebroretinal syndrome		HP:0001336	OMIM:274240	IEA					P	HPO:iea[2009-02-17]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0002553	PMID:25439727	PCS		1/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000252	PMID:25439727	PCS		3/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0002059	PMID:25439727	PCS		1/3			P	HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000343	PMID:25439727	PCS		2/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0002188	PMID:25439727	PCS		1/3			P	HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0002376	PMID:25439727	PCS		1/1			P	HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0001250	PMID:25439727	PCS		3/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0001263	PMID:25439727	PCS		3/3		HP:0012828	P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0001252	PMID:25439727	PCS		2/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0001285	PMID:25439727	PCS		3/3			P	HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000280	PMID:25439727	PCS		1/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000518	PMID:25439727	PCS		2/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000508	PMID:25439727	PCS		1/3			P	HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000316	PMID:25439727	PCS		1/3			P	HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000007	PMID:25439727	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0001305	PMID:25439727	PCS		1/3			P	HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000219	PMID:25439727	PCS		1/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0000400	PMID:25439727	PCS		1/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0001510	PMID:25439727	PCS		3/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0001257	PMID:25439727	PCS		3/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2021-07-01]
OMIM:616154	Peroxisomal fatty acyl-CoA reductase 1 disorder		HP:0006855	PMID:25439727	PCS		1/3			P	HPO:probinson[2021-07-01]
OMIM:118450	Alagille syndrome 1		HP:0001297	OMIM:118450	TAS					P	HPO:skoehler[2013-05-31]
OMIM:118450	Alagille syndrome 1		HP:0000486	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0000089	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0001492	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0001252	PMID:31157196	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000482	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0003593	PMID:31157196;PMID:34071626	PCS		3/5			C	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000081	PMID:12509572	PCS		2/187			P	HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0000518	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0011463	PMID:34071626	PCS		2/4			C	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0002937	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0003829	OMIM:118450	TAS					I	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0000316	PMID:34071626	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0001328	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0008659	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0001920	PMID:12509572	PCS		2/187			P	HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0001402	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0000772	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0002155	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0003124	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0000490	PMID:34071626	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000097	PMID:12509572	PCS		2/187			P	HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0001738	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0004969	PMID:31157196;PMID:34071626	PCS		5/5			P	HPO:probinson[2022-05-14];HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000400	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0000006	PMID:9207787	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000369	PMID:34071626	IEA		1/1			P	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000325	PMID:34071626	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0003774	PMID:12509572	PCS		4/187			P	HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0001396	PMID:34071626	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000582	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0000585	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0001399	PMID:12509572	PCS		38/174			P	HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0001394	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0000580	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0001508	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0001629	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0001947	PMID:22105858	PCS		7/187			P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0006571	PMID:34071626	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0011120	PMID:31157196	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0009882	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0000337	PMID:34071626	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0000414	PMID:31157196	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0004617	PMID:34071626	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0002910	PMID:31157196	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0006579	OMIM:118450	TAS					P	HPO:skoehler[2013-06-03]
OMIM:118450	Alagille syndrome 1		HP:0000533	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0000110	PMID:22105858	PCS		43/187			P	HPO:iea[2009-02-17];HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0000593	OMIM:118450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:118450	Alagille syndrome 1		HP:0002895	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0000076	PMID:22105858	PCS		6/187			P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-23]
OMIM:118450	Alagille syndrome 1		HP:0000750	PMID:31157196	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0003189	PMID:34071626	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0003022	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0001284	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0001680	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0011344	PMID:31157196	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0005280	OMIM:118450	TAS					P	HPO:skoehler[2012-11-25]
OMIM:118450	Alagille syndrome 1		HP:0000627	PMID:34071626	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0001636	OMIM:118450	IEA					P	HPO:skoehler[2010-06-18]
OMIM:118450	Alagille syndrome 1		HP:0002007	PMID:31157196	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:118450	Alagille syndrome 1		HP:0001631	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:118450	Alagille syndrome 1		HP:0000545	OMIM:118450	IEA					P	HPO:iea[2009-02-17]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0000132	PMID:21917754;PMID:9845537	PCS		11/11			P	HPO:probinson[2022-03-31];HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0001892	PMID:9845537	PCS		1/1			P	HPO:probinson[2022-03-31]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0003010	PMID:20020534	PCS					P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0031126	PMID:16463284	PCS		35/37			P	HPO:probinson[2021-05-29];HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0011871	PMID:16463284	PCS		0/40			P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0008320	PMID:16463284	PCS		40/40			P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0006298	PMID:21917754	PCS					P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0000007	PMID:2014236	PCS					I	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0000978	PMID:21917754;PMID:9845537	PCS		11/11			P	HPO:probinson[2022-03-31];HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0008148	PMID:16463284	PCS		40/40			P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0004846	PMID:21917754	PCS					P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0000421	PMID:21917754	PCS					P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0001975	PMID:20020534;PMID:2014236	PCS		21/27			P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0004866	PMID:16463284	PCS		40/40			P	HPO:probinson[2021-05-29]
OMIM:619267	Glanzmann thrombasthenia 2		HP:0003623	PMID:9845537	PCS		1/1			C	HPO:probinson[2022-03-31]
OMIM:254190	Myasthenia, congenital, refractory to acetylcholinesterase inhibitors		HP:0003473	OMIM:254190	TAS					P	HPO:skoehler[2015-01-21]
OMIM:254190	Myasthenia, congenital, refractory to acetylcholinesterase inhibitors		HP:0001939	OMIM:254190	IEA					P	HPO:iea[2009-02-17]
OMIM:254190	Myasthenia, congenital, refractory to acetylcholinesterase inhibitors		HP:0007970	OMIM:254190	IEA					P	HPO:iea[2009-02-17]
OMIM:254190	Myasthenia, congenital, refractory to acetylcholinesterase inhibitors		HP:0000007	OMIM:254190	IEA					I	HPO:iea[2009-02-17]
OMIM:254190	Myasthenia, congenital, refractory to acetylcholinesterase inhibitors		HP:0003701	OMIM:254190	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254190	Myasthenia, congenital, refractory to acetylcholinesterase inhibitors		HP:0000544	OMIM:254190	IEA					P	HPO:iea[2009-02-17]
OMIM:160500	Myopathy, distal, 1		HP:0010628	OMIM:160500	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:160500	Myopathy, distal, 1		HP:0003236	PMID:17548557	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0011916	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:160500	Myopathy, distal, 1		HP:0003593	OMIM:160500	IEA		1/1			C	HPO:iea[2012-04-11];HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0002460	OMIM:160500	TAS					P	HPO:probinson[2012-04-11]
OMIM:160500	Myopathy, distal, 1		HP:0011399	PMID:17548557	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0031295	PMID:17548557	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0011463	OMIM:160500	IEA					C	HPO:iea[2009-02-17]
OMIM:160500	Myopathy, distal, 1		HP:0002938	PMID:17548557	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0003805	OMIM:160500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:160500	Myopathy, distal, 1		HP:0003803	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:160500	Myopathy, distal, 1		HP:0000218	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:160500	Myopathy, distal, 1		HP:0003701	OMIM:160500	TAS		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:160500	Myopathy, distal, 1		HP:0003326	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:160500	Myopathy, distal, 1		HP:0001644	OMIM:160500	TAS		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:160500	Myopathy, distal, 1		HP:0001265	PMID:17548557	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0003445	OMIM:160500	TAS					P	HPO:probinson[2012-04-11]
OMIM:160500	Myopathy, distal, 1		HP:0002650	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:160500	Myopathy, distal, 1		HP:0003200	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:160500	Myopathy, distal, 1		HP:0001761	OMIM:160500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:160500	Myopathy, distal, 1		HP:0001288	OMIM:160500	IEA					P	HPO:iea[2009-02-17]
OMIM:160500	Myopathy, distal, 1		HP:0008180	OMIM:160500	TAS					P	HPO:skoehler[2013-01-21]
OMIM:160500	Myopathy, distal, 1		HP:0009053	PMID:17548557	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0009031	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:160500	Myopathy, distal, 1		HP:0009077	PMID:17548557	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0030051	PMID:17548557	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0003677	OMIM:160500	IEA					C	HPO:iea[2009-02-17]
OMIM:160500	Myopathy, distal, 1		HP:0000006	PMID:15322983	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-09-24]
OMIM:160500	Myopathy, distal, 1		HP:0000467	OMIM:160500	TAS					P	HPO:probinson[2012-06-08]
OMIM:611808	Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus		HP:0001288	OMIM:611808	IEA					P	HPO:iea[2009-02-17]
OMIM:611808	Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus		HP:0002343	OMIM:611808	IEA					P	HPO:iea[2009-02-17]
OMIM:611808	Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus		HP:0030186	OMIM:611808	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611808	Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus		HP:0002119	OMIM:611808	IEA					P	HPO:iea[2009-02-17]
OMIM:611808	Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus		HP:0000256	OMIM:611808	IEA					P	HPO:iea[2009-02-17]
OMIM:611808	Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus		HP:0000006	OMIM:611808	IEA					I	HPO:iea[2009-02-17]
OMIM:611808	Tremor, hereditary essential, and idiopathic normal pressure hydrocephalus		HP:0001337	OMIM:611808	TAS					P	HPO:skoehler[2009-02-17]
OMIM:614970	Joubert syndrome 20		HP:0003577	PMID:23012439	PCS		3/3			C	HPO:skoehler[2013-01-21];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0001344	PMID:23012439	PCS		3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0002540	PMID:23012439	PCS		3/3			P	HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0001263	PMID:23012439	PCS		3/3			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0004692	PMID:23012439	PCS		2/3			P	HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0002093	PMID:23012439	PCS		3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0100259	PMID:23012439	PCS		2/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0000718	PMID:23012439	PCS		1/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0000657	PMID:23012439	PCS		3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0000107	PMID:23012439	PCS		2/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0000007	PMID:23012439	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0002419	PMID:23012439	PCS		3/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0000488	PMID:23012439	PCS		2/3			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-11-07]
OMIM:614970	Joubert syndrome 20		HP:0000742	PMID:23012439	PCS		1/3			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0002169	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0001252	PMID:7668837	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0003593	PMID:8554662	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0031008	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0100034	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0031206	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0011463	PMID:7668837	PCS		2/2			C	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0001427	PMID:8554662	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0002359	PMID:8554662	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0002315	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0000597	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0001348	PMID:7668837	PCS		2/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0001249	PMID:7668837	PCS		2/2			P	HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0000654	OMIM:500003	IEA					P	HPO:iea[2009-02-17]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0002311	PMID:7668837	PCS		2/4			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0003200	OMIM:500003	IEA					P	HPO:iea[2009-02-17]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0003487	PMID:8554662;PMID:7668837	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0001288	PMID:8554662	PCS	HP:0011463	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0000273	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0001263	PMID:8554662;PMID:7668837	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-05];HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0002151	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0002072	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0040196	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0007098	OMIM:500003	TAS					P	HPO:probinson[2009-02-17]
OMIM:500003	Striatonigral degeneration, infantile, mitochondrial		HP:0001336	PMID:7668837	PCS		1/2			P	HPO:probinson[2022-04-05]
OMIM:212890	Cerebellar ataxia, benign, with thermoanalgesia		HP:0003584	OMIM:212890	TAS					C	HPO:skoehler[2009-02-17]
OMIM:212890	Cerebellar ataxia, benign, with thermoanalgesia		HP:0010829	OMIM:212890	TAS	HP:0003584				P	HPO:probinson[2012-07-25]
OMIM:212890	Cerebellar ataxia, benign, with thermoanalgesia		HP:0000007	OMIM:212890	IEA					I	HPO:iea[2009-02-17]
OMIM:212890	Cerebellar ataxia, benign, with thermoanalgesia		HP:0002073	OMIM:212890	IEA	HP:0003584				P	HPO:iea[2009-02-17]
OMIM:212890	Cerebellar ataxia, benign, with thermoanalgesia		HP:0003447	OMIM:212890	TAS					P	HPO:skoehler[2009-02-17]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000286	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002465	OMIM:616801	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001531	PMID:26708753	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002540	OMIM:616801	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001250	OMIM:616801	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0003273	OMIM:616801	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001290	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0012389	PMID:26708753	PCS		6/6			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000639	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000319	PMID:26545877	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0011220	PMID:26545877	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002019	PMID:26708751	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000358	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000297	PMID:26708751	PCS		4/4			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000252	PMID:26708753	PCS		3/6			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000494	OMIM:616801	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001344	PMID:26708751	PCS		4/4			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002079	PMID:26708751	PCS		1/4			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0011968	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0012736	PMID:26708753	PCS		6/6			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001182	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0100660	OMIM:616801	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000448	PMID:26545877	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000007	PMID:26708753	PCS					I	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000565	PMID:26708751	PCS		3/4			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001257	PMID:26708753	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000322	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000369	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000325	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000248	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0004326	PMID:26708753	PCS		6/6			P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001276	PMID:26708753	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000463	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002283	PMID:26708753	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000938	PMID:26708753	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0007069	PMID:26708753	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000337	PMID:26545877	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000414	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000219	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002059	OMIM:616801	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002650	OMIM:616801	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000194	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000470	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0011344	OMIM:616801	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000508	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000426	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0000348	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001357	PMID:26545877	PCS					P	HPO:probinson[2017-06-18]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0001511	OMIM:616801	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616801	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2		HP:0002007	OMIM:616801	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0003236	PMID:30283131	PCS		5/9			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0000365	PMID:30283131	PCS		1/1			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0008163	PMID:30283131	PCS		1/2			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0001640	PMID:30283131	PCS		9/9			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0001903	PMID:30283131	PCS		7/7			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0001790	PMID:30283131	IEA	HP:0011461	3/9			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0000007	PMID:30283131	PCS					I	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0001943	PMID:30283131	PCS		2/9			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0001511	PMID:30283131	PCS	HP:0011461	2/9			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0001622	PMID:30283131	PCS		2/9			P	HPO:probinson[2020-06-28]
OMIM:618838	Combined oxidative phosphorylation deficiency 41		HP:0003128	PMID:30283131	PCS		9/9			P	HPO:probinson[2020-06-28]
OMIM:101840	Acrokeratoderma, hereditary papulotranslucent		HP:0002213	OMIM:101840	TAS					P	HPO:probinson[2015-01-31]
OMIM:101840	Acrokeratoderma, hereditary papulotranslucent		HP:0012393	OMIM:101840	TAS					P	HPO:probinson[2015-01-31]
OMIM:101840	Acrokeratoderma, hereditary papulotranslucent		HP:0200035	OMIM:101840	TAS					P	HPO:probinson[2015-01-31]
OMIM:101840	Acrokeratoderma, hereditary papulotranslucent		HP:0200034	OMIM:101840	TAS					P	HPO:probinson[2015-01-31]
OMIM:101840	Acrokeratoderma, hereditary papulotranslucent		HP:0000006	OMIM:101840	TAS					I	HPO:probinson[2009-02-17]
OMIM:176410	Precocious puberty, male		HP:0008185	PMID:7692306	PCS	HP:0011463		MALE		P	HPO:iea[2009-02-17];HPO:probinson[2020-11-29]
OMIM:176410	Precocious puberty, male		HP:0001470	PMID:7692306	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-29]
OMIM:176410	Precocious puberty, male		HP:0008734	OMIM:176410	TAS					P	HPO:iea[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0002069	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000286	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0004322	OMIM:257300	PCS					P	HPO:probinson[2012-03-16]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001250	PMID:15475955	PCS		2/10			P	HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0003196	OMIM:257300	TAS					P	HPO:skoehler[2013-08-10]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001290	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000518	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000639	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000316	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000238	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0006872	PMID:15475955	PCS		1/10			P	HPO:probinson[2012-03-16];HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0008897	OMIM:257300	PCS					P	HPO:probinson[2012-03-16]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0200024	OMIM:257300	TAS					P	HPO:probinson[2012-05-05]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000879	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001642	PMID:15475955	PCS		1/10			P	HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000358	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000175	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000252	PMID:15475955	PCS		9/9		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000054	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0005387	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0011800	OMIM:257300	TAS					P	HPO:skoehler[2013-11-28]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000007	PMID:15475955	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000207	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000048	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0002667	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000047	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0006743	PMID:15475955	PCS		2/10			P	HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000003	PMID:15475955	PCS		1/10			P	HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000248	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000369	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000445	OMIM:257300	TAS					P	HPO:skoehler[2013-08-10]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000582	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000343	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000463	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0002123	OMIM:257300	PCS					P	HPO:probinson[2012-03-16]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000062	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0006849	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0030674	PMID:15475955	PCS		9/9			C	HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001274	OMIM:257300	TAS					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001909	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001305	OMIM:257300	TAS					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0008872	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0002119	OMIM:257300	PCS					P	HPO:probinson[2012-03-16]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001562	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001321	OMIM:257300	TAS					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000272	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000470	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0011344	OMIM:257300	PCS					P	HPO:probinson[2012-03-16]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0005280	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001518	PMID:15475955	PCS		9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000107	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000348	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001511	PMID:15475955	PCS		9/9			P	HPO:probinson[2012-03-16];HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0001631	PMID:15475955	PCS		2/10			P	HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000028	OMIM:257300	IEA					P	HPO:probinson[2009-02-17]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0000347	OMIM:257300	PCS					P	HPO:probinson[2012-03-16]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0002445	PMID:15475955	PCS		2/10			P	HPO:probinson[2022-11-01]
OMIM:257300	Mosaic variegated aneuploidy syndrome 1		HP:0002247	PMID:15475955	PCS		1/10			P	HPO:probinson[2022-11-01]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0007183	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0002376	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0001332	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0000639	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0001263	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0001252	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0002151	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0001251	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0001427	OMIM:500017	TAS					I	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0008972	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:500017	Mitochondrial Leigh syndrome		HP:0000648	OMIM:500017	TAS					P	HPO:probinson[2024-12-14]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0001880	PMID:16607617	PCS		3/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0002312	PMID:16607617	PCS		2/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0003236	PMID:16607617	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0010628	OMIM:253600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0003621	PMID:16607617	PCS		4/6			C	HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0001288	OMIM:253600	IEA					P	HPO:iea[2009-02-17]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0001371	OMIM:253600	IEA					P	HPO:iea[2009-02-17]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0003691	OMIM:253600	IEA					P	HPO:iea[2009-02-17]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0003560	PMID:16607617	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0032019	PMID:16607617	PCS		6/6			P	HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0007340	PMID:16607617	PCS		2/6			P	HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0011463	PMID:16607617	PCS		2/6			C	HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0100614	PMID:16607617	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0000007	PMID:7720071	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:253600	Muscular dystrophy, limb-girdle, type 2A		HP:0007126	OMIM:253600	IEA					P	HPO:iea[2009-02-17]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000286	PMID:27818385;OMIM:618186	PCS		11/13			P	HPO:probinson[2023-04-07];HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0003577	PMID:27818385	PCS		3/3			C	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0003431	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000365	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000189	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001332	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001272	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001371	OMIM:618186	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001250	OMIM:618186	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0002020	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000817	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0012471	PMID:27818385	PCS		1/3			P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000338	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001349	PMID:27818385	PCS		1/3			P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0002878	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0003429	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000218	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000212	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000278	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001347	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001760	OMIM:618186	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001188	OMIM:618186	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001265	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000252	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001561	PMID:27818385	PCS		1/3			P	HPO:skoehler[2019-04-18]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0003487	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0002079	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0003121	OMIM:618186	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001284	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0004691	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0002093	OMIM:618186	IEA	HP:0003623				P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000508	PMID:27818385	PCS		1/3			P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0002804	OMIM:618186	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000007	PMID:27818385	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001558	PMID:27818385	PCS		1/3			P	HPO:skoehler[2019-04-18]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000505	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000268	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0003811	PMID:27818385	PCS		2/3			C	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001257	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000369	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0000347	OMIM:618186	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0001776	PMID:27818385	PCS		1/3			P	HPO:probinson[2023-04-07]
OMIM:618186	Neuropathy, congenital hypomyelinating, 3		HP:0004326	OMIM:618186	IEA					P	HPO:skoehler[2019-04-18]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0000473	OMIM:249670	IEA					P	HPO:skoehler[2010-06-20]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0000232	OMIM:249670	IEA					P	HPO:iea[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0004322	OMIM:249670	IEA					P	HPO:iea[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0001629	OMIM:249670	IEA					P	HPO:iea[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0001161	OMIM:249670	IEA					P	HPO:skoehler[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0003241	OMIM:249670	IEA					P	HPO:iea[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0000007	OMIM:249670	IEA					I	HPO:iea[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0004150	OMIM:249670	IEA					P	HPO:skoehler[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0001643	OMIM:249670	IEA					P	HPO:iea[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0001631	OMIM:249670	IEA					P	HPO:iea[2009-02-17]
OMIM:249670	Mesoaxial hexadactyly and cardiac malformation		HP:0001642	OMIM:249670	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212112	Malouf syndrome		HP:0001058	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0000331	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0000460	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0011838	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0031610	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0100585	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0034681	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0000815	OMIM:212112	TAS					P	HPO:skoehler[2009-02-17]
OMIM:212112	Malouf syndrome		HP:0011463	PMID:17150192	PCS		1/1			C	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0000938	OMIM:212112	IEA					P	HPO:skoehler[2019-09-07]
OMIM:212112	Malouf syndrome		HP:0008551	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0000508	OMIM:212112	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:212112	Malouf syndrome		HP:0009125	OMIM:212112	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212112	Malouf syndrome		HP:0001638	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0200021	OMIM:212112	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212112	Malouf syndrome		HP:0001653	PMID:17150192	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:212112	Malouf syndrome		HP:0000278	OMIM:212112	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212112	Malouf syndrome		HP:0000894	OMIM:212112	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212112	Malouf syndrome		HP:0000006	PMID:17150192	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0001249	OMIM:212112	TAS		HP:0040283			P	HPO:skoehler[2014-02-06]
OMIM:212112	Malouf syndrome		HP:0001029	PMID:17150192	PCS		1/1			P	HPO:probinson[2023-04-07]
OMIM:212112	Malouf syndrome		HP:0001644	OMIM:212112	TAS					P	HPO:skoehler[2010-06-20]
OMIM:620357	Diarrhea 13		HP:0001397	PMID:33191500	PCS		5/5			P	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0002013	PMID:33191500	PCS		5/5			P	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0001508	PMID:33191500	PCS		5/5			P	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0001988	PMID:33191500	PCS		5/5			P	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0003073	PMID:33191500	PCS		5/5			P	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0000007	PMID:33191500	PCS					I	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0005208	PMID:33191500	PCS		5/5			P	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0002910	PMID:33191500	PCS		5/5			P	HPO:probinson[2023-07-01]
OMIM:620357	Diarrhea 13		HP:0003623	PMID:33191500	PCS		5/5			C	HPO:probinson[2023-07-01]
OMIM:252250	Monocyte chemotactic disorder		HP:0001939	OMIM:252250	IEA					P	HPO:iea[2009-02-17]
OMIM:252250	Monocyte chemotactic disorder		HP:0002728	OMIM:252250	IEA					P	HPO:iea[2009-02-17]
OMIM:252250	Monocyte chemotactic disorder		HP:0000007	OMIM:252250	IEA					I	HPO:iea[2009-02-17]
OMIM:252250	Monocyte chemotactic disorder		HP:0002965	OMIM:252250	IEA					P	HPO:iea[2009-02-17]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001298	PMID:31727539	PCS		26/26			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0003477	PMID:31727539	PCS		5/7			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0006989	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000463	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001250	PMID:31727539	PCS		10/21			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000160	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001252	PMID:31727539	PCS		16/16			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0002240	PMID:31727539	PCS		4/4			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0045075	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000519	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0008872	PMID:31727539	PCS		4/6			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0025116	PMID:31727539	PCS	HP:0011461	12/18			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001561	PMID:31727539	PCS	HP:0011461	12/18			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000054	PMID:31727539	PCS			MALE		P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000431	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001321	PMID:31727539	PCS		17/24			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0002299	PMID:31727539	PCS		6/11			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0003146	PMID:31727539	PCS		2/2			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000034	PMID:31727539	PCS			MALE		P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001263	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0002151	PMID:31727539	PCS		17/19			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001639	PMID:31727539	PCS		8/15			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000007	PMID:31727539	PCS					I	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0003811	PMID:31727539	PCS		15/26			C	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0001257	PMID:31727539	PCS		5/5			P	HPO:probinson[2020-06-13]
OMIM:618810	Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal		HP:0000347	PMID:31727539	PCS					P	HPO:probinson[2020-06-13]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000286	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001650	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0004325	PMID:38479391	PCS		3/10			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0002664	PMID:38479391	PCS		0/13			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000365	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001651	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0004322	PMID:38479391	PCS		1/11			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001250	PMID:38479391	PCS		1/12			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001252	PMID:38479391	PCS		5/13			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0003196	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000085	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000041	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0011611	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0011577	PMID:38479391	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0033725	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0034188	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000716	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000717	PMID:38479391	PCS		5/11			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0012076	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0002539	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000316	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0025732	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001643	PMID:38479391	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000278	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001642	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001249	PMID:38479391	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000358	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000494	PMID:38479391	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000252	PMID:38479391	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0002197	PMID:38479391	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000490	PMID:38479391	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001263	PMID:38479391	PCS		13/13			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0030746	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0034396	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0004969	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0007874	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000768	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0007359	PMID:38479391	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000047	PMID:38479391	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000960	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000322	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000369	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0002665	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000006	PMID:38479391	PCS					I	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001655	PMID:38479391	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000341	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000582	PMID:38479391	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0004467	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000343	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0004388	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0005235	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000463	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0002164	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000020	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0100033	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001629	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000739	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001746	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0006695	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001748	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000750	PMID:38479391	PCS		11/11			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0003189	PMID:38479391	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000276	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000034	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0200006	PMID:38479391	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0002092	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0005281	PMID:38479391	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0005280	PMID:38479391	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0400005	PMID:38479391	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001518	PMID:38479391	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001636	PMID:38479391	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0002007	PMID:38479391	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001631	PMID:38479391	PCS		2/13			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0007018	PMID:38479391	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0001873	PMID:38479391	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:621049	Pan-Chung-Bellen syndrome		HP:0000028	PMID:38479391	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-09-26]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0012529	PMID:11830488	PCS		14/14			P	HP:probinson[2019-03-03];HP:probinson[2019-03-03]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0003540	PMID:11830488	PCS		14/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-03]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0003010	PMID:11830488	PCS		14/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-03]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0031364	PMID:18478040	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0012527	PMID:11830488	PCS					P	HP:probinson[2019-03-03]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0012524	PMID:18478040	PCS		0/1			P	HP:probinson[2019-03-03];HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0011870	PMID:18478040	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0011463	PMID:18478040	PCS		1/1			C	HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0000979	PMID:18478040	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0004808	PMID:11830488	PCS		3/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-03]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0008320	PMID:18478040	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0000978	OMIM:601399	IEA					P	HPO:iea[2009-02-17]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0000967	PMID:18478040	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0004845	PMID:18478040	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0000421	OMIM:601399	TAS					P	HPO:probinson[2009-02-17]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0001873	OMIM:601399	TAS		1/1			P	HPO:probinson[2009-02-17]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0000006	PMID:11830488	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-03]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0004866	PMID:18478040	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0002665	OMIM:601399	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0002863	OMIM:601399	IEA					P	HPO:iea[2009-02-17]
OMIM:601399	Platelet disorder, familial, with associated myeloid malignancy		HP:0003006	OMIM:601399	IEA					P	HPO:iea[2009-02-17]
OMIM:142945	Holoprosencephaly 3		HP:0009914	OMIM:142945	IEA					P	HPO:iea[2012-04-24]
OMIM:142945	Holoprosencephaly 3		HP:0000252	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0000175	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0001360	OMIM:142945	IEA					P	HPO:iea[2012-04-24]
OMIM:142945	Holoprosencephaly 3		HP:0000193	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0002000	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0012806	OMIM:142945	TAS					P	HPO:skoehler[2014-06-24]
OMIM:142945	Holoprosencephaly 3		HP:0001263	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0000272	OMIM:142945	IEA					P	HPO:iea[2012-04-24]
OMIM:142945	Holoprosencephaly 3		HP:0011800	OMIM:142945	TAS					P	HPO:skoehler[2013-11-28]
OMIM:142945	Holoprosencephaly 3		HP:0410030	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0005280	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0003829	OMIM:142945	IEA					I	HPO:iea[2010-03-10]
OMIM:142945	Holoprosencephaly 3		HP:0000601	OMIM:142945	IEA					P	HPO:iea[2012-04-24]
OMIM:142945	Holoprosencephaly 3		HP:0002119	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0000366	OMIM:142945	IEA					P	HPO:iea[2012-04-24]
OMIM:142945	Holoprosencephaly 3		HP:0000520	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0009932	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0000006	OMIM:142945	IEA					I	HPO:iea[2012-04-24]
OMIM:142945	Holoprosencephaly 3		HP:0006315	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0001249	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:142945	Holoprosencephaly 3		HP:0000126	OMIM:142945	IEA					P	HPO:iea[2012-04-24]
OMIM:142945	Holoprosencephaly 3		HP:0000863	OMIM:142945	IEA					P	HPO:skoehler[2019-09-07]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0000819	OMIM:211369	IEA					P	HPO:iea[2009-02-17]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0000252	OMIM:211369	IEA					P	HPO:iea[2009-02-17]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0009372	OMIM:211369	IEA					P	HPO:probinson[2010-06-20]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0001250	OMIM:211369	IEA					P	HPO:iea[2009-02-17]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0000007	OMIM:211369	IEA					I	HPO:iea[2009-02-17]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0009576	OMIM:211369	TAS					P	HPO:probinson[2013-04-14]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0005726	OMIM:211369	IEA					P	HPO:iea[2009-02-17]
OMIM:211369	Brachydactyly, type A2, with microcephaly		HP:0005824	OMIM:211369	IEA					P	HPO:iea[2009-02-17]
OMIM:613951	Fanconi anemia, complementation group P		HP:0001045	OMIM:613951	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000252	PMID:21240277	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000365	PMID:21240277	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0004322	OMIM:613951	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613951	Fanconi anemia, complementation group P		HP:0002860	OMIM:613951	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613951	Fanconi anemia, complementation group P		HP:0003221	PMID:21240277	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000581	OMIM:613951	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000085	PMID:21240277	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0012745	PMID:21240277	PCS		1/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0001903	PMID:21240277	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000957	PMID:21240277	PCS		1/4			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000007	PMID:21240277	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000414	PMID:21240277	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0009777	OMIM:613951	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000125	OMIM:613951	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613951	Fanconi anemia, complementation group P		HP:0001510	PMID:21240277	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0009778	PMID:21240277	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000028	OMIM:613951	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613951	Fanconi anemia, complementation group P		HP:0002984	OMIM:613951	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613951	Fanconi anemia, complementation group P		HP:0000347	PMID:21240277	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-04]
OMIM:613951	Fanconi anemia, complementation group P		HP:0001876	PMID:21240277	PCS		3/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-04]
OMIM:613789	Complement component 8 deficiency, type II		HP:0001287	OMIM:613789	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613789	Complement component 8 deficiency, type II		HP:0004434	OMIM:613789	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613789	Complement component 8 deficiency, type II		HP:0005430	OMIM:613789	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613789	Complement component 8 deficiency, type II		HP:0000007	OMIM:613789	TAS					I	HPO:skoehler[2012-10-17]
OMIM:620343	Basal cell nevus syndrome 2		HP:0001067	PMID:36825822	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0003577	PMID:19533801	PCS		1/2			C	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0003764	PMID:19533801	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0010615	PMID:36825822	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0002321	PMID:36825822	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0002076	PMID:36825822	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0002671	PMID:36825822	PCS		2/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0003581	PMID:36825822	PCS		2/2			C	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0005462	PMID:19533801;PMID:36825822	PCS		2/4			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0010610	PMID:19533801;PMID:36825822	PCS		3/4			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0010612	PMID:19533801	PCS		2/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0011462	PMID:19533801	PCS		1/2			C	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0002858	PMID:36825822	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0000238	PMID:19533801	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0200034	PMID:36825822	PCS		2/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0002007	PMID:19533801	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0000256	PMID:19533801	PCS		2/2			P	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0000006	PMID:19533801	PCS					I	HPO:probinson[2023-07-10]
OMIM:620343	Basal cell nevus syndrome 2		HP:0002885	PMID:19533801	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:609909	Cardiomyopathy, dilated, 1P		HP:0011462	PMID:12610310	PCS		20/20			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:609909	Cardiomyopathy, dilated, 1P		HP:0001635	PMID:12610310	PCS		12/20			P	HPO:probinson[2013-03-31];HPO:probinson[2022-07-03]
OMIM:609909	Cardiomyopathy, dilated, 1P		HP:0006673	OMIM:609909	TAS					P	HPO:probinson[2013-03-31]
OMIM:609909	Cardiomyopathy, dilated, 1P		HP:0004308	OMIM:609909	TAS					P	HPO:probinson[2013-03-31]
OMIM:609909	Cardiomyopathy, dilated, 1P		HP:0000006	PMID:12610310	PCS					I	HPO:probinson[2013-03-31];HPO:probinson[2020-07-21]
OMIM:609909	Cardiomyopathy, dilated, 1P		HP:0001644	PMID:12610310	PCS		20/20			P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-21];HPO:probinson[2022-07-03]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000252	OMIM:600093	IEA					P	HPO:iea[2009-02-17]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000431	OMIM:600093	TAS					P	HPO:probinson[2012-05-01]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0001263	OMIM:600093	IEA					P	HPO:iea[2009-02-17]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000007	OMIM:600093	IEA					I	HPO:iea[2009-02-17]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0005715	OMIM:600093	IEA					P	HPO:iea[2009-02-17]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000455	OMIM:600093	TAS					P	HPO:probinson[2012-05-01]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000179	OMIM:600093	IEA					P	HPO:iea[2009-02-17]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000322	OMIM:600093	TAS					P	HPO:probinson[2009-02-17]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000289	OMIM:600093	TAS					P	HPO:probinson[2012-05-01]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0000215	OMIM:600093	IEA					P	HPO:iea[2012-05-01]
OMIM:600093	Spondyloepiphyseal dysplasia tarda with characteristic facies		HP:0002655	OMIM:600093	TAS					P	HPO:iea[2009-02-17]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0001397	PMID:29321044;PMID:26833330	PCS		5/5			P	HPO:probinson[2017-06-17];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0010837	PMID:29321044;PMID:26833330	PCS		7/7			P	HPO:probinson[2017-06-17];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0031956	PMID:29321044;PMID:26833330	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type Iip		HP:0003236	PMID:29321044	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0003621	PMID:26833330	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0001410	OMIM:616829	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0003124	PMID:29321044;PMID:26833330	PCS		6/7			P	HPO:probinson[2017-06-17];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0003155	PMID:29321044;PMID:26833330	PCS		7/7			P	HPO:probinson[2017-06-17];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0001263	PMID:29321044;PMID:26833330	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-05-11];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0001395	PMID:29321044;PMID:26833330	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0001252	PMID:29321044;PMID:26833330	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0003141	PMID:29321044;PMID:26833330	PCS		6/7			P	HPO:probinson[2017-06-17];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0025321	PMID:29321044;PMID:26833330	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type Iip		HP:0002240	PMID:29321044;PMID:26833330	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0003593	PMID:29321044;PMID:26833330	PCS		2/7			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type Iip		HP:0011967	PMID:29321044	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0012301	PMID:29321044;PMID:26833330	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0012347	PMID:26833330	PCS		4/4			P	HPO:probinson[2017-06-17]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0012358	PMID:26833330	PCS		3/4			P	HPO:probinson[2017-06-17]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0031964	PMID:29321044;PMID:26833330	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type Iip		HP:0011463	PMID:29321044	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0000007	PMID:26833330	PCS					I	HPO:probinson[2017-06-17]
OMIM:616829	Congenital disorder of glycosylation, type IIp		HP:0002910	PMID:26833330	PCS		4/4			P	HPO:probinson[2017-06-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000286	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000341	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0002188	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000243	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0011236	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0011682	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000519	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0002878	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0002119	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0030084	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000218	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0006610	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000278	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0002553	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0002353	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000431	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0002079	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0005487	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000470	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0011623	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0012385	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0011272	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0001838	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0001518	PMID:32021605	IEA		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0011451	PMID:32021605	PCS	HP:0030674	2/2			P	HPO:probinson[2020-05-17];HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0011230	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000007	PMID:32021605	PCS					I	HPO:probinson[2020-05-17];HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000568	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0001558	PMID:32021605	PCS	HP:0030674				P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0007598	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0025325	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000444	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000202	PMID:32021605	PCS		1/2			P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0001511	PMID:32021605	PCS					P	HPO:probinson[2020-05-17]
OMIM:618804	Sandestig-Stefanova syndrome		HP:0000369	PMID:32021605	PCS		2/2			P	HPO:probinson[2020-05-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000242	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001176	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0004322	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001290	OMIM:264090	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000639	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000518	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0100807	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000238	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001324	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000358	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000494	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002155	OMIM:264090	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000771	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000490	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002308	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000007	OMIM:264090	IEA					I	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0003758	PMID:21671373	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000883	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000520	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000369	PMID:21671373	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000248	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001276	PMID:21671373	PCS		4/5			P	HPO:probinson[2022-05-08];HPO:skoehler[2019-04-18];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000582	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001792	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0003577	OMIM:264090;PMID:21671373	PCS		13/13			C	HPO:probinson[2022-05-08];HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000343	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000463	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000460	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001274	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002080	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001305	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0030084	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000336	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000472	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002015	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000233	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002650	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001684	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0003100	PMID:21671373	PCS		7/7			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001043	PMID:21671373	PCS		10/10			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08];HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000592	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000470	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0030088	OMIM:264090	TAS					P	HPO:skoehler[2014-09-21]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002090	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0011229	OMIM:264090	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0100678	PMID:21671373	PCS		3/3			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0007495	PMID:21671373	PCS		7/7			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001833	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002007	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000347	PMID:21671373	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000621	PMID:21671373	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000561	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002223	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000684	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000040	PMID:21671373	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001371	OMIM:264090	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000160	OMIM:264090	TAS					P	HPO:skoehler[2012-11-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001252	OMIM:264090	TAS					P	HPO:skoehler[2014-11-26]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0045075	OMIM:264090	TAS					P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000958	PMID:21671373	PCS		3/3			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000319	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0011220	PMID:21671373	PCS		3/3			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0007485	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000316	PMID:21671373	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001249	OMIM:264090	TAS					P	HPO:skoehler[2012-11-21]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0003700	PMID:21671373	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002078	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000695	OMIM:264090	TAS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0011968	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001263	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0010511	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0004492	PMID:21671373	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0100578	OMIM:264090	TAS					P	HPO:skoehler[2012-11-21]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000601	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000444	PMID:21671373	PCS		7/7			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000047	OMIM:264090	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000325	PMID:21671373	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000963	PMID:21671373	PCS		3/3			P	HPO:skoehler[2012-11-22];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000385	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001476	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000387	PMID:21671373	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001596	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0003097	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0005792	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001508	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000418	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000778	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000656	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002714	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000653	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000774	PMID:21671373	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000256	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0003269	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001762	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002970	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002692	PMID:21671373	PCS		8/10			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000272	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0045025	PMID:21671373	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002293	PMID:21671373	PCS		3/3			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0005280	PMID:21671373	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001518	PMID:21671373	PCS		7/7			P	HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000946	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002209	PMID:21671373	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000668	OMIM:264090	IEA					P	HPO:skoehler[2019-04-18]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000307	PMID:21671373	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-08]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0002205	OMIM:264090	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0001511	OMIM:264090	IEA					P	HPO:iea[2009-02-17]
OMIM:264090	Wiedemann-Rautenstrauch syndrome		HP:0000028	PMID:21671373	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0003577	PMID:32554502	PCS		2/2			C	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0012574	PMID:32554502	PCS		1/2			P	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0000100	PMID:32554502	PCS		2/2			P	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0001321	PMID:32554502	PCS		1/2			P	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0000518	PMID:32554502	PCS		2/2			P	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0004387	PMID:32554502	PCS		2/2			P	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0003819	PMID:32554502	PCS		2/2			C	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0000097	PMID:32554502	PCS		1/2			P	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0000007	PMID:32554502	PCS					I	HPO:probinson[2024-03-01]
OMIM:620425	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2		HP:0003429	PMID:32554502	PCS		1/2			P	HPO:probinson[2024-03-01]
OMIM:611820	Long QT syndrome 11		HP:0003621	PMID:18093912	PCS		1/1			C	HPO:probinson[2022-07-09]
OMIM:611820	Long QT syndrome 11		HP:0005184	PMID:18093912	PCS		4/4			P	HPO:probinson[2022-07-09]
OMIM:611820	Long QT syndrome 11		HP:0001279	PMID:18093912	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-09]
OMIM:611820	Long QT syndrome 11		HP:0000006	PMID:18093912	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-09]
OMIM:216360	Coach syndrome 1		HP:0003774	PMID:19058225	PCS		3/12			P	HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0003577	PMID:19058225	PCS		12/12			C	HPO:probinson[2022-03-24]
OMIM:216360	Coach syndrome 1		HP:0000463	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0000122	PMID:19058225	PCS		1/12			P	HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001332	PMID:19058225	PCS		2/12			P	HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001250	OMIM:216360	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:216360	Coach syndrome 1		HP:0002085	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0001252	PMID:19058225	PCS		10/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001395	PMID:19058225	PCS	HP:0003577	10/12			P	HPO:skoehler[2013-06-06];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0003593	OMIM:216360	TAS					C	HPO:skoehler[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0001394	OMIM:216360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:216360	Coach syndrome 1		HP:0002240	PMID:19058225	PCS		9/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001251	PMID:19058225	PCS		8/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001290	OMIM:216360	TAS					P	HPO:skoehler[2017-07-13]
OMIM:216360	Coach syndrome 1		HP:0002040	PMID:19058225	PCS		3/12			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0002084	PMID:19058225	PCS		2/12			P	HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0033149	PMID:19058225	PCS		2/12			P	HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001409	OMIM:216360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:216360	Coach syndrome 1		HP:0000639	PMID:19058225	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000316	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0000657	PMID:19058225	PCS		9/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0002617	OMIM:216360	IEA					P	HPO:skoehler[2018-10-08]
OMIM:216360	Coach syndrome 1		HP:0002419	PMID:19058225	PCS		10/12			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000311	OMIM:216360	IEA					P	HPO:skoehler[2010-06-20]
OMIM:216360	Coach syndrome 1		HP:0002910	PMID:19058225	PCS		9/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001744	OMIM:216360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:216360	Coach syndrome 1		HP:0008659	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0001347	PMID:19058225	PCS		5/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000154	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0001320	OMIM:216360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:216360	Coach syndrome 1		HP:0001162	PMID:19058225	PCS		1/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0006817	PMID:19058225	PCS		3/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001263	PMID:19058225	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000090	PMID:19058225	PCS		5/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000508	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0000822	OMIM:216360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:216360	Coach syndrome 1		HP:0001438	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0000107	PMID:19058225	PCS		1/12			P	HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000007	PMID:19058225	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000543	PMID:19058225	PCS		1/12			P	HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0001257	OMIM:216360	IEA					P	HPO:iea[2009-02-17]
OMIM:216360	Coach syndrome 1		HP:0001510	PMID:19058225	PCS		4/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:216360	Coach syndrome 1		HP:0000589	PMID:19058225	PCS		5/12			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:112800	Brachydactyly, type A4		HP:0009370	OMIM:112800	TAS					P	HPO:probinson[2009-02-17]
OMIM:112800	Brachydactyly, type A4		HP:0005850	OMIM:112800	TAS					P	HPO:probinson[2009-02-17]
OMIM:112800	Brachydactyly, type A4		HP:0004220	OMIM:112800	TAS					P	HPO:probinson[2012-06-09]
OMIM:112800	Brachydactyly, type A4		HP:0009577	OMIM:112800	TAS					P	HPO:probinson[2012-06-09]
OMIM:112800	Brachydactyly, type A4		HP:0100387	OMIM:112800	TAS					P	HPO:probinson[2009-02-17]
OMIM:112800	Brachydactyly, type A4		HP:0001884	OMIM:112800	TAS	HP:0003577				P	HPO:probinson[2012-06-09]
OMIM:112800	Brachydactyly, type A4		HP:0000006	OMIM:112800	TAS					I	HPO:probinson[2009-02-17]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001397	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20];HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0002136	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001531	PMID:32004446	PCS	HP:0003593				P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0000750	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0002188	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001321	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001263	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0002240	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0003073	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001270	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0031964	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0000518	PMID:32004446	PCS	HP:0003577	3/4			P	HPO:probinson[2020-05-20];HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0000007	PMID:32004446	PCS					I	HPO:probinson[2020-05-20];HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0000568	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0006673	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001935	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001733	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0001644	PMID:32004446	PCS		1/4			P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0002028	PMID:32004446	PCS	HP:0003593				P	HPO:probinson[2020-05-20]
OMIM:618805	Triokinase and FMN cyclase deficiency syndrome		HP:0003128	PMID:32004446	PCS					P	HPO:probinson[2020-05-20]
OMIM:178400	Pulmonary edema of mountaineers		HP:0100598	OMIM:178400	IEA					P	HPO:skoehler[2015-01-27]
OMIM:178400	Pulmonary edema of mountaineers		HP:0000969	OMIM:178400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:178400	Pulmonary edema of mountaineers		HP:0002086	OMIM:178400	IEA					P	HPO:iea[2009-02-17]
OMIM:178400	Pulmonary edema of mountaineers		HP:0004890	OMIM:178400	IEA					P	HPO:iea[2009-02-17]
OMIM:178400	Pulmonary edema of mountaineers		HP:0000006	OMIM:178400	IEA					I	HPO:iea[2009-02-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0003236	OMIM:616828	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001399	PMID:26833332	PCS		2/5			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001250	PMID:26833332	PCS		1/4			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0025321	PMID:26833332	PCS					P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001394	OMIM:616828	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0002240	OMIM:616828	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0003593	OMIM:616828	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001290	PMID:26833332	PCS		3/4			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0012345	PMID:26833332	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0002910	PMID:26833332	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001744	OMIM:616828	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0006579	OMIM:616828	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0002611	OMIM:616828	TAS				HP:0003676	P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0003202	OMIM:616828	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0010639	PMID:26833332	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0010837	PMID:26833332	PCS		3/3			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0000494	OMIM:616828	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0003124	PMID:26833332	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0000276	OMIM:616828	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0003141	PMID:26833332	PCS		5/5			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001263	PMID:26833332	PCS		3/4			P	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0000508	OMIM:616828	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001999	OMIM:616828	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0000007	PMID:26833332	PCS					I	HPO:probinson[2017-06-17]
OMIM:616828	Congenital disorder of glycosylation, type IIO		HP:0001433	PMID:26833332	PCS		3/5			P	HPO:probinson[2017-06-17]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0002069	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0001320	PMID:24784881;PMID:30912300	PCS		3/4			P	HP:probinson[2021-10-16];HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0003510	PMID:24784881	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0003236	PMID:30912300	PCS		2/2			P	HP:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0000252	PMID:24784881;PMID:30912300	PCS		4/4			P	HP:probinson[2021-10-16];HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0002983	PMID:24784881	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0000582	PMID:24784881;PMID:30912300	PCS		4/4			P	HP:probinson[2021-10-16];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0005621	PMID:30912300	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0025681	PMID:30912300	PCS		2/2			P	HPO:probinson[2022-02-03]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0001156	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0001591	PMID:24784881	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0002164	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0001260	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0001252	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0003394	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0010049	PMID:15578577	PCS					P	HPO:probinson[2012-06-03];HPO:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0033725	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0000007	PMID:24784881	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0007676	PMID:24784881	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0000037	PMID:24784881	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0000774	PMID:24784881	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0007359	PMID:30912300	PCS		1/2			P	HP:probinson[2021-10-16]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0009803	PMID:24784881	PCS		2/2			P	HPO:probinson[2012-06-03];HPO:probinson[2021-02-18]
OMIM:600092	Nivelon-Nivelon-Mabille syndrome		HP:0000588	PMID:24784881	PCS		2/2			P	HPO:probinson[2021-02-18]
OMIM:620342	Cone-rod dystrophy 24		HP:0003596	PMID:11006213;PMID:35947183	PCS		2/2			C	HPO:probinson[2023-07-10];HPO:probinson[2023-07-10];HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000662	PMID:11006213;PMID:35947183	PCS		2/3			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000551	PMID:11006213	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0030499	PMID:35947183	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000580	PMID:23563732	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0011463	PMID:23563732	PCS		1/1			C	HPO:probinson[2023-07-10];HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000608	PMID:35947183	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0007761	PMID:11006213	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000613	PMID:23563732;PMID:11006213	PCS		2/3			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0007663	PMID:11006213	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0007401	PMID:11006213	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000548	PMID:11006213;PMID:35947183	PCS		2/3			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0007843	PMID:23563732	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000575	PMID:35947183	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000006	PMID:11006213	PCS					I	HPO:probinson[2023-07-10]
OMIM:620342	Cone-rod dystrophy 24		HP:0000545	PMID:11006213	PCS		1/2			P	HPO:probinson[2023-07-10]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000684	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000365	OMIM:135500	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000040	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001250	PMID:25915598	PCS		6/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001252	PMID:25915598;OMIM:135500	PCS		14/16			P	HPO:probinson[2022-04-22];HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0002020	PMID:25915598	PCS		2/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000280	PMID:25915598	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000518	OMIM:135500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0012471	PMID:25915598	PCS		2/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0002616	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001643	OMIM:135500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001007	PMID:25915598	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000358	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0002553	PMID:25915598	PCS		2/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001187	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000574	PMID:25915598	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000293	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000294	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001537	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001857	PMID:25915598	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000169	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000322	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000006	PMID:25915598	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000369	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001792	PMID:25915598	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000343	PMID:25915598	PCS		2/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0005113	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0003298	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0002240	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001507	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0009882	PMID:25915598	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000657	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000337	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000218	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0002714	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000455	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000212	PMID:25915598	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000256	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001744	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000154	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0002650	PMID:25915598	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000431	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0100874	PMID:25915598	PCS		2/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000348	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001638	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000664	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000268	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000303	OMIM:135500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000545	OMIM:135500	IEA					P	HPO:iea[2009-02-17]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000787	OMIM:135500	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0000666	PMID:25915598	PCS		1/6			P	HPO:probinson[2022-04-22]
OMIM:135500	Zimmermann-Laband syndrome 1		HP:0001798	PMID:25915598	PCS		3/5			P	HPO:probinson[2022-04-22]
OMIM:613950	Schizophrenia 15		HP:0003621	PMID:20385823	PCS		1/4			C	HPO:probinson[2022-10-03]
OMIM:613950	Schizophrenia 15		HP:0100753	PMID:20385823	PCS		4/4			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-10-03]
OMIM:613950	Schizophrenia 15		HP:0011462	PMID:20385823	PCS		3/4			C	HPO:probinson[2022-10-03]
OMIM:613950	Schizophrenia 15		HP:0000752	PMID:20385823	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-03]
OMIM:613950	Schizophrenia 15		HP:0000006	PMID:20385823	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-03]
OMIM:613950	Schizophrenia 15		HP:0001249	PMID:20385823	PCS		2/4			P	HPO:probinson[2022-10-03]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002169	OMIM:614959	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0003676	PMID:24029078	PCS					C	HPO:skoehler[2012-12-30];HPO:probinson[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002188	PMID:24029078;PMID:23086397	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-05-21];HPO:probinson[2023-03-18];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002266	PMID:24029078;PMID:23086397	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002120	PMID:24029078;PMID:23086397	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-05-21];HPO:skoehler[2012-12-30];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0001252	PMID:23086397	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0003593	PMID:24029078;PMID:23086397	PCS		4/8			C	ORCID:0000-0002-0736-9199[2024-05-21];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0001290	PMID:24029078;PMID:23086397	PCS		4/8			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0032773	PMID:24029078;PMID:23086397	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0012444	PMID:24029078	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0032677	PMID:24029078	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0033725	PMID:24029078;PMID:23086397	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0011182	PMID:24029078	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0011167	PMID:24029078;PMID:23086397	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0000817	PMID:23086397	PCS		HP:0040283			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0001347	OMIM:614959	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0003623	PMID:23086397	PCS		4/6			C	HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0008936	PMID:24029078;PMID:23086397	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0000252	PMID:24029078;PMID:23086397	PCS		4/8			P	HPO:skoehler[2012-12-30];ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0001344	PMID:24029078;PMID:23086397	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002133	OMIM:614959	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002376	PMID:24029078	PCS		1/2			P	HPO:skoehler[2013-01-22];HPO:probinson[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002079	PMID:23086397	PCS		7/12			P	HPO:skoehler[2012-12-30];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0006915	PMID:24029078;PMID:23086397	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0010818	PMID:24029078;PMID:23086397	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-05-21];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002171	OMIM:614959	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0011169	PMID:24029078;PMID:23086397	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0012736	PMID:24029078;PMID:23086397	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-05-21];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0011154	PMID:23086397	PCS		5/12			P	HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0011153	PMID:24029078;PMID:23086397	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-21];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002529	OMIM:614959	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0200134	PMID:24029078;PMID:23086397	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-05-21];HPO:skoehler[2015-01-19];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0001257	OMIM:614959	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0000006	PMID:23086397	PCS					I	HPO:skoehler[2012-12-30];HPO:probinson[2023-03-18]
OMIM:614959	Developmental and epileptic encephalopathy 14		HP:0002445	OMIM:614959	TAS					P	HPO:skoehler[2012-12-30]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002663	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001176	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000089	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002020	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003593	PMID:21474761	PCS		1/10			C	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0010049	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0045028	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000238	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0006872	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000878	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002536	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000113	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000237	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003865	OMIM:210710	TAS					P	HPO:probinson[2012-07-18]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000890	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000252	PMID:21474761	PCS		10/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0100258	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002827	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000926	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000007	PMID:21474760	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001338	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000520	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0009616	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000369	OMIM:210710	TAS					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003577	PMID:21474761	PCS		3/10			C	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000340	OMIM:210710	IEA		2/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000463	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001156	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001274	PMID:21474761	PCS		6/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003051	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0008070	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0100702	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001302	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0006579	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001320	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001562	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0006956	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0009826	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002133	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0005487	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001680	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000470	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002093	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0011623	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000107	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001833	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001954	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000347	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002126	PMID:21474761	PCS		4/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002344	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002983	OMIM:210710	TAS					P	HPO:skoehler[2012-10-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002980	OMIM:210710	TAS					P	HPO:probinson[2012-07-18]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001773	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001371	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001250	OMIM:210710	IEA		1/10			P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003273	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0045075	OMIM:210710	TAS					P	HPO:probinson[2022-05-07]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000958	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000954	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003826	OMIM:210710	IEA					C	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0008850	PMID:21474761	PCS					P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001522	PMID:21474761	PCS		1/10			C	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000311	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002335	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001249	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000054	PMID:21474761	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002750	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002079	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000331	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0011968	PMID:21474761	PCS		2/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003044	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003042	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0032327	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0006380	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002904	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000448	OMIM:210710	TAS					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002987	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000322	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0009778	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000962	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001655	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003498	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0030674	PMID:21474761	PCS		6/10			C	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003097	OMIM:210710	TAS					P	HPO:probinson[2015-03-21]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0005792	OMIM:210710	TAS					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002282	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001508	PMID:21474761	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0007185	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001629	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0008551	PMID:21474761	PCS		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0004616	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000653	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001623	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002213	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0030048	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0003819	PMID:21474761	PCS		2/10			C	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000946	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000822	PMID:21474761	PCS		2/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0002209	OMIM:210710	TAS					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001636	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0007333	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0006487	PMID:21474761	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0006400	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001511	PMID:21474761	PCS		6/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0001631	OMIM:210710	IEA		1/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000028	OMIM:210710;PMID:21474761	PCS		11/20			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-04]
OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		HP:0000269	OMIM:210710	IEA					P	HPO:probinson[2009-02-17]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0000276	OMIM:300271	IEA					P	HPO:iea[2009-02-17]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0004322	PMID:20159109	PCS		4/9			P	HPO:probinson[2021-08-30];HPO:probinson[2021-08-30]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0001250	PMID:20159109	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-08-30]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0001419	PMID:20159109	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-08-30]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0001263	PMID:20159109	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-08-30]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0000729	PMID:20159109	PCS		1/9			P	HPO:probinson[2021-08-30]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0000733	OMIM:300271	IEA					P	HPO:iea[2009-02-17]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0000268	OMIM:300271	IEA					P	HPO:iea[2009-02-17]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0000752	OMIM:300271	IEA					P	HPO:iea[2009-02-17]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0000256	PMID:20159109	PCS		6/9			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-08-30]
OMIM:300271	Intellectual developmental disorder, X-linked 72		HP:0001249	PMID:20159109	PCS		9/9	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2021-08-30]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0002850	PMID:36006710	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0001045	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0001025	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0002783	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0410297	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0030783	PMID:36006710	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0001890	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0011839	PMID:36006710	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0003593	PMID:36006710	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0034797	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0100651	PMID:36006710	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0010975	PMID:36006710	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0012476	PMID:36006710	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0011463	PMID:36006710	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0033199	PMID:36006710	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0040089	PMID:36006710	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0000403	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0001954	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0000821	PMID:36006710	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0000007	PMID:36006710	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0002720	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620430	Autoimmune disease, multisystem, infantile-onset, 3		HP:0004315	PMID:36006710	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:202300	Adrenocortical carcinoma, pediatric		HP:0030392	PMID:18762572	PCS	HP:0003593	1/1			P	HPO:probinson[2022-05-14]
OMIM:202300	Adrenocortical carcinoma, pediatric		HP:0006744	PMID:18762572	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:202300	Adrenocortical carcinoma, pediatric		HP:0000006	PMID:18762572	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-14]
OMIM:602849	Muenke syndrome		HP:0000486	PMID:26740388	PCS		31/69			P	HPO:skoehler[2018-10-08];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000365	PMID:26740388	PCS		69/89			P	HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0004322	PMID:9042914	PCS		0/34			P	HPO:probinson[2024-03-10]
OMIM:602849	Muenke syndrome		HP:0003795	OMIM:602849	IEA					P	HPO:iea[2009-02-17]
OMIM:602849	Muenke syndrome		HP:0001156	PMID:26740388	PCS		11/48			P	HPO:skoehler[2014-11-26];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0001250	PMID:26740388	PCS		20/99			P	HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0004440	PMID:9042914	PCS		33/49			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:602849	Muenke syndrome		HP:0006193	PMID:26740388;PMID:9042914	PCS		22/37			P	HPO:probinson[2024-03-10];HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0010055	PMID:26740388;PMID:9042914	PCS		45/104			P	HPO:probinson[2024-03-10];HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0010230	PMID:26740388;PMID:9042914	PCS		8/25			P	HPO:probinson[2024-03-10];HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000316	PMID:26740388	PCS		39/82			P	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0009466	OMIM:602849	IEA					P	HPO:iea[2009-02-17]
OMIM:602849	Muenke syndrome		HP:0000218	PMID:26740388;PMID:9042914	PCS		64/133			P	HPO:probinson[2024-03-10];HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0030084	PMID:26740388	PCS		10/47			P	HPO:skoehler[2014-09-21];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000256	PMID:26740388	PCS		19/86			P	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0001249	PMID:26740388	PCS		31/87			P	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0002676	PMID:26740388	PCS		0/86			P	HP:probinson[2019-04-18];HPO:probinson[2024-03-10]
OMIM:602849	Muenke syndrome		HP:0000494	PMID:9042914	PCS		17/34			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:602849	Muenke syndrome		HP:0001263	PMID:26740388	PCS		63/95			P	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0001241	OMIM:602849	IEA					P	HPO:iea[2009-02-17]
OMIM:602849	Muenke syndrome		HP:0000272	OMIM:602849	IEA					P	HPO:iea[2009-02-17]
OMIM:602849	Muenke syndrome		HP:0000294	OMIM:602849	IEA					P	HPO:iea[2009-02-17]
OMIM:602849	Muenke syndrome		HP:0011800	PMID:26740388;PMID:9042914	PCS		53/83			P	HPO:probinson[2024-03-10];HPO:skoehler[2013-11-28];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0032569	PMID:20301588	PCS					P	HPO:probinson[2019-09-07]
OMIM:602849	Muenke syndrome		HP:0011304	PMID:26740388	PCS		14/46			P	HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000407	PMID:9042914	PCS		17/46			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:602849	Muenke syndrome		HP:0005819	OMIM:602849	IEA					P	HPO:iea[2009-02-17]
OMIM:602849	Muenke syndrome		HP:0000508	PMID:26740388	PCS		11/83			P	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000646	PMID:26740388	PCS		20/135			P	HP:probinson[2019-04-18];HP:probinson[2019-04-18];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000403	PMID:26740388	PCS		34/55			P	HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000689	OMIM:602849	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602849	Muenke syndrome		HP:0001357	PMID:26740388	PCS		16/86			P	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000520	PMID:26740388	PCS		5/81			P	HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0007018	PMID:26740388	PCS		14/59			P	HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000248	PMID:26740388	PCS		47/86			P	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:602849	Muenke syndrome		HP:0000006	PMID:26740388	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-18]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0003774	OMIM:613944	TAS					P	HPO:skoehler[2013-07-01]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0000794	OMIM:613944	TAS					P	HPO:skoehler[2013-07-01]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0000123	OMIM:613944	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0002829	OMIM:613944	TAS		HP:0040283			P	HPO:skoehler[2013-07-01]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0000790	OMIM:613944	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0003829	PMID:17186473	PCS					I	HPO:lccarmody[2019-04-19]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0000822	OMIM:613944	TAS					P	HPO:skoehler[2013-07-01]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0000093	OMIM:613944	TAS					P	HPO:skoehler[2013-07-01]
OMIM:613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2		HP:0000006	PMID:17186473	PCS					I	HPO:lccarmody[2019-04-19]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0002169	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0002650	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0003693	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0001284	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0002460	PMID:29517768	PCS	HP:0011463	1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:6000335	PMID:29517768	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0030319	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0009130	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0001508	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0032341	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0040078	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0009027	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0000007	PMID:29517768	PCS					I	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0003648	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0001935	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0001308	PMID:29517768	PCS		1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0002527	PMID:29517768	PCS	HP:0011463	1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:618811	Mitochondrial DNA depletion syndrome 18		HP:0003701	PMID:29517768	PCS	HP:0003621	1/1			P	HPO:probinson[2020-06-06];HPO:probinson[2020-06-06]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0034011	PMID:35543642;PMID:34476482	PCS		4/4			P	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0032560	PMID:35543642	PCS		1/1			P	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0003251	PMID:35543642;PMID:34476482	PCS		4/4			P	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0000007	PMID:34476482	PCS					I	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0012207	PMID:34476482	PCS		3/3			P	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0011109	PMID:35543642;PMID:34476482	PCS		4/4			P	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0012257	PMID:35543642;PMID:34476482	PCS		4/4			P	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0004469	PMID:35543642;PMID:34476482	PCS		4/4			P	HPO:probinson[2023-07-01]
OMIM:620356	Ciliary dyskinesia, primary, 50		HP:0032559	PMID:35543642	PCS		1/1			P	HPO:probinson[2023-07-01]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0003236	PMID:30283131	PCS		5/9			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001410	PMID:30283131	PCS		5/9			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0000365	PMID:30283131	PCS		1/1			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0011924	PMID:30283131	PCS					P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001790	PMID:30283131	IEA	HP:0030674	3/9			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0011923	PMID:30283131	PCS					P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0008163	PMID:30283131	PCS		1/2			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001903	PMID:30283131	PCS		7/7			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0000007	PMID:30283131	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001943	PMID:30283131	PCS		2/9			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001638	PMID:30283131	PCS		9/9			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0008347	PMID:30283131	PCS					P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001511	PMID:30283131	PCS	HP:0011461	2/9			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0003811	PMID:30283131	PCS		3/9			C	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001522	PMID:30283131	PCS		6/9			C	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0001622	PMID:30283131	PCS	HP:0003577	2/9			P	HPO:probinson[2020-07-19]
OMIM:618839	Combined oxidative phosphorylation deficiency 42		HP:0003128	PMID:30283131	PCS		9/9			P	HPO:probinson[2020-07-19]
OMIM:616814	Preimplantation embryonic lethality 1		HP:0008222	PMID:26537248	TAS					P	HPO:lccarmody[2019-01-29]
OMIM:616814	Preimplantation embryonic lethality 1		HP:0000007	OMIM:616814	TAS					I	HPO:skoehler[2017-07-13]
OMIM:203750	Alpha-methylacetoacetic aciduria		HP:0005974	OMIM:203750	IEA					P	HPO:iea[2009-02-17]
OMIM:203750	Alpha-methylacetoacetic aciduria		HP:4000204	OMIM:203750	TAS					P	HPO:probinson[2024-01-06]
OMIM:203750	Alpha-methylacetoacetic aciduria		HP:0002013	OMIM:203750	IEA					P	HPO:iea[2009-02-17]
OMIM:203750	Alpha-methylacetoacetic aciduria		HP:0001944	OMIM:203750	IEA					P	HPO:iea[2009-02-17]
OMIM:203750	Alpha-methylacetoacetic aciduria		HP:0000007	OMIM:203750	IEA					I	HPO:iea[2009-02-17]
OMIM:203750	Alpha-methylacetoacetic aciduria		HP:0001249	OMIM:203750	IEA					P	HPO:iea[2009-02-17]
OMIM:203750	Alpha-methylacetoacetic aciduria		HP:6000603	PMID:9700610	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:618187	Ovarian dysgenesis 8		HP:0000939	PMID:30113650	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618187	Ovarian dysgenesis 8		HP:0025708	PMID:30113650	PCS		1/1			C	HPO:probinson[2023-06-08]
OMIM:618187	Ovarian dysgenesis 8		HP:0011969	PMID:30113650	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:618187	Ovarian dysgenesis 8		HP:0003782	PMID:30113650	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:618187	Ovarian dysgenesis 8		HP:0008232	PMID:30113650	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:618187	Ovarian dysgenesis 8		HP:0008214	PMID:30113650	PCS		1/1			P	HPO:probinson[2023-06-08]
OMIM:618187	Ovarian dysgenesis 8		HP:0031103	PMID:30113650	PCS		1/1			P	HPO:probinson[2023-06-08]
OMIM:618187	Ovarian dysgenesis 8		HP:0000059	PMID:30113650	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:618187	Ovarian dysgenesis 8		HP:0000006	PMID:30113650	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-08]
OMIM:618187	Ovarian dysgenesis 8		HP:0000786	PMID:30113650	PCS		1/1			P	HPO:skoehler[2019-02-15]
OMIM:608394	Deafness, autosomal dominant 43		HP:0000407	OMIM:608394	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608394	Deafness, autosomal dominant 43		HP:0000360	OMIM:608394	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608394	Deafness, autosomal dominant 43		HP:0000006	OMIM:608394	TAS					I	HPO:skoehler[2017-07-13]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003202	PMID:9009996	PCS		7/7			P	HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003236	PMID:9731527	PCS		25/25			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003555	OMIM:253601	IEA					P	HPO:iea[2009-02-17]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003621	PMID:9731527;PMID:9009996	PCS		11/17			C	HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003551	OMIM:253601	IEA					P	HPO:iea[2009-02-17]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003560	PMID:9731527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0012378	OMIM:253601	IEA					P	HPO:skoehler[2018-10-08]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0009025	OMIM:253601	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0011462	PMID:9731527;PMID:9009996	PCS		16/17			C	HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0009046	OMIM:253601	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0000007	PMID:9731527	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0002505	PMID:9731527	PCS		6/25			P	HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0002505	PMID:9009996	PCS	HP:0003596	6/7			P	HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003701	PMID:9731527;PMID:9009996	PCS		32/32			P	HPO:probinson[2022-09-07];HPO:probinson[2022-09-07];HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003677	OMIM:253601	IEA					C	HPO:iea[2009-02-17]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003458	PMID:9731527	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-07]
OMIM:253601	Muscular dystrophy, limb-girdle, type 2B		HP:0003557	OMIM:253601	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001265	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003236	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0010628	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003200	PMID:7726154	PCS		1/1			P	HPO:probinson[2013-12-08];HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003487	PMID:7726154	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001288	PMID:7726154	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0012507	OMIM:500002	TAS					P	HPO:probinson[2013-12-09]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001260	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001252	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001251	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001290	OMIM:500002	TAS					P	HPO:skoehler[2017-07-13]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003690	PMID:7726154	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001270	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0001427	PMID:7726154	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0008347	OMIM:500002	TAS					P	HPO:probinson[2013-12-08]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0025710	PMID:7726154	PCS		1/1			C	HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003737	OMIM:500002	TAS					P	HPO:skoehler[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0007126	OMIM:500002	TAS					P	HPO:skoehler[2012-10-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003701	OMIM:500002	IEA					P	HPO:skoehler[2010-06-18]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0005978	PMID:7726154	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003688	PMID:7726154	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003458	OMIM:500002	IEA					P	HPO:iea[2009-02-17]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0003546	PMID:7726154	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:500002	Mitochondrial myopathy with diabetes		HP:0000467	PMID:7726154	PCS		1/1			P	HPO:probinson[2022-10-03]
OMIM:611809	Bestrophinopathy, autosomal recessive		HP:0012045	PMID:18179881	PCS					P	HPO:probinson[2013-04-03]
OMIM:611809	Bestrophinopathy, autosomal recessive		HP:0000540	PMID:18179881	PCS					P	HPO:probinson[2013-04-03]
OMIM:611809	Bestrophinopathy, autosomal recessive		HP:0000007	PMID:18179881	PCS					I	HPO:probinson[2013-01-09]
OMIM:611809	Bestrophinopathy, autosomal recessive		HP:0007663	PMID:18179881	PCS					P	HPO:probinson[2013-04-03]
OMIM:611809	Bestrophinopathy, autosomal recessive		HP:0007722	PMID:18179881	PCS					P	HPO:probinson[2015-07-19]
OMIM:611809	Bestrophinopathy, autosomal recessive		HP:0000654	PMID:18179881	PCS					P	HPO:probinson[2013-04-03]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002135	PMID:15883308	PCS		4/4			P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002476	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002353	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0003487	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0001288	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002079	PMID:15883308	PCS		5/6			P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002354	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002120	PMID:15883308	PCS		6/6			P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002340	PMID:15883308	PCS		2/6			P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002186	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0001250	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002352	PMID:15883308	PCS		6/6			P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002381	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0010524	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002829	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0012062	PMID:15883308	PCS					P	HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0000726	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0012690	PMID:15883308	PCS		4/6			P	HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0000938	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0000734	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0000007	PMID:15883308	PCS					I	HPO:probinson[2020-11-26]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0002756	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0007305	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618193	Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2		HP:0001336	PMID:15883308	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:608380	Retinitis pigmentosa 26		HP:0001133	PMID:14681825	PCS					P	HPO:probinson[2013-03-24]
OMIM:608380	Retinitis pigmentosa 26		HP:0000007	PMID:14681825	PCS					I	HPO:probinson[2013-01-09]
OMIM:608380	Retinitis pigmentosa 26		HP:0000505	PMID:14681825	PCS					P	HPO:probinson[2013-03-24]
OMIM:608380	Retinitis pigmentosa 26		HP:0000543	PMID:14681825	PCS					P	HPO:probinson[2013-03-24]
OMIM:608380	Retinitis pigmentosa 26		HP:0007688	PMID:14681825	PCS					P	HPO:probinson[2013-03-24]
OMIM:608380	Retinitis pigmentosa 26		HP:0000510	OMIM:608380	TAS					P	HPO:skoehler[2015-01-21]
OMIM:608380	Retinitis pigmentosa 26		HP:0007843	PMID:14681825	PCS					P	HPO:probinson[2013-03-24]
OMIM:147800	Aase-Smith syndrome I		HP:0000175	OMIM:147800	IEA					P	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0001762	OMIM:147800	IEA					P	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0000194	OMIM:147800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147800	Aase-Smith syndrome I		HP:0001371	OMIM:147800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147800	Aase-Smith syndrome I		HP:0001629	OMIM:147800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147800	Aase-Smith syndrome I		HP:0000508	OMIM:147800	IEA					P	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0000238	OMIM:147800	IEA					P	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0001305	OMIM:147800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147800	Aase-Smith syndrome I		HP:0001522	OMIM:147800	IEA					C	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0006742	OMIM:147800	IEA					P	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0000377	OMIM:147800	IEA					P	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0000006	OMIM:147800	IEA					I	HPO:iea[2009-02-17]
OMIM:147800	Aase-Smith syndrome I		HP:0001238	OMIM:147800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0003015	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0007516	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0006009	OMIM:602875	TAS					P	HPO:probinson[2013-04-07]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001377	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0003196	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001230	OMIM:602875	TAS					P	HPO:probinson[2012-06-03]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0010049	OMIM:602875	TAS					P	HPO:probinson[2012-06-03]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0010743	OMIM:602875	TAS					P	HPO:probinson[2012-05-08]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0010230	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0011220	OMIM:602875	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0002938	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0008873	PMID:25959430	PCS		9/9			P	HPO:probinson[2024-03-10]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001847	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001500	OMIM:602875	IEA					P	HPO:iea[2012-06-03]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0009803	OMIM:602875	TAS		20/20			P	HPO:probinson[2013-04-07];HPO:iea[2012-06-03]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001249	PMID:25959430	PCS		0/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-10]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0004633	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0003300	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001783	OMIM:602875	TAS					P	HPO:probinson[2012-05-08]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001382	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0003086	PMID:25959430	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-10]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0008484	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0000007	OMIM:602875	IEA					I	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0005619	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0002007	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0002986	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001799	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0002984	OMIM:602875	TAS					P	HPO:probinson[2012-06-03]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0004568	OMIM:602875	IEA					P	HPO:iea[2009-02-17]
OMIM:602875	Acromesomelic dysplasia, Maroteaux type		HP:0001831	OMIM:602875	TAS		20/20			P	HPO:probinson[2012-06-03];HPO:iea[2009-02-17]
OMIM:613978	Hemoglobin H disease		HP:0011907	OMIM:613978	TAS					P	HPO:probinson[2013-02-23]
OMIM:613978	Hemoglobin H disease		HP:0011903	OMIM:613978	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613978	Hemoglobin H disease		HP:0002240	OMIM:613978	TAS					P	HPO:probinson[2013-02-23]
OMIM:613978	Hemoglobin H disease		HP:0001878	OMIM:613978	TAS					P	HPO:probinson[2013-01-09]
OMIM:613978	Hemoglobin H disease		HP:0001744	OMIM:613978	TAS					P	HPO:probinson[2013-02-23]
OMIM:231090	Hydatidiform mole, recurrent, 1		HP:0032192	PMID:16462743	PCS		5/5			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-08-04]
OMIM:231090	Hydatidiform mole, recurrent, 1		HP:0005268	PMID:16462743	PCS		2/5			C	HPO:probinson[2022-08-04]
OMIM:231090	Hydatidiform mole, recurrent, 1		HP:0011462	PMID:16462743	PCS		5/5			C	HPO:probinson[2022-08-04]
OMIM:231090	Hydatidiform mole, recurrent, 1		HP:0000007	PMID:16462743	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:231090	Hydatidiform mole, recurrent, 1		HP:0032468	PMID:16462743	PCS		2/5			H	HPO:probinson[2022-08-04]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0003202	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0002015	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0002398	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0001260	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0003581	OMIM:105400	TAS					C	HPO:probinson[2022-07-19]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0003394	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0002380	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0010535	OMIM:105400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0007354	PMID:8446170	PCS					P	HPO:skoehler[2015-01-19];HP:probinson[2019-03-03]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0007024	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0000007	OMIM:105400	IEA					I	HPO:skoehler[2012-10-12]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0001324	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0001257	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0000006	PMID:8446170	PCS					I	HPO:probinson[2012-04-11];HP:probinson[2019-03-03]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0002314	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:105400	Amyotrophic lateral sclerosis 1		HP:0001347	OMIM:105400	TAS					P	HPO:probinson[2012-04-11]
OMIM:172850	Piebald trait with neurologic defects		HP:0000365	OMIM:172850	IEA					P	HPO:iea[2009-02-17]
OMIM:172850	Piebald trait with neurologic defects		HP:0002211	OMIM:172850	IEA					P	HPO:iea[2009-02-17]
OMIM:172850	Piebald trait with neurologic defects		HP:0001251	OMIM:172850	IEA					P	HPO:iea[2009-02-17]
OMIM:172850	Piebald trait with neurologic defects		HP:0007542	OMIM:172850	IEA					P	HPO:iea[2009-02-17]
OMIM:172850	Piebald trait with neurologic defects		HP:0000006	OMIM:172850	IEA					I	HPO:iea[2009-02-17]
OMIM:172850	Piebald trait with neurologic defects		HP:0001249	OMIM:172850	IEA					P	HPO:iea[2009-02-17]
OMIM:148500	Tylosis with esophageal cancer		HP:0003621	PMID:22265016	PCS					C	HPO:probinson[2022-11-26]
OMIM:148500	Tylosis with esophageal cancer		HP:0001036	OMIM:148500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148500	Tylosis with esophageal cancer		HP:0007447	PMID:22265016	PCS	HP:0003621				P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:148500	Tylosis with esophageal cancer		HP:0002745	PMID:22265016	PCS					P	HPO:probinson[2022-11-26]
OMIM:148500	Tylosis with esophageal cancer		HP:0007502	PMID:22265016	PCS					P	HPO:probinson[2022-11-26]
OMIM:148500	Tylosis with esophageal cancer		HP:0000006	PMID:22265016	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:148500	Tylosis with esophageal cancer		HP:0011459	PMID:22265016	PCS	HP:0003581				P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:619500	Deafness, autosomal dominant 81		HP:0001751	PMID:29713870	PCS		0/9			P	HPO:probinson[2021-09-04];HPO:probinson[2021-09-04]
OMIM:619500	Deafness, autosomal dominant 81		HP:0000407	PMID:29713870	PCS		9/9			P	HPO:probinson[2021-09-04];HPO:probinson[2021-09-04]
OMIM:619500	Deafness, autosomal dominant 81		HP:0011462	PMID:29713870	PCS					C	HPO:probinson[2021-09-04]
OMIM:619500	Deafness, autosomal dominant 81		HP:0000006	PMID:29713870	PCS					I	HPO:probinson[2021-09-04];HPO:probinson[2021-09-04]
OMIM:606346	Deafness, autosomal dominant 22		HP:0000408	OMIM:606346	TAS					P	HPO:skoehler[2015-12-30]
OMIM:606346	Deafness, autosomal dominant 22		HP:0000407	OMIM:606346	TAS					P	HPO:probinson[2013-01-09]
OMIM:606346	Deafness, autosomal dominant 22		HP:0000006	OMIM:606346	TAS					I	HPO:probinson[2013-03-24]
OMIM:185200	Striae distensae, familial		HP:0001065	OMIM:185200	TAS					P	HPO:probinson[2009-02-17]
OMIM:185200	Striae distensae, familial		HP:0000006	OMIM:185200	TAS					I	HPO:probinson[2009-02-17]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0001265	PMID:25439726	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0003621	PMID:25439726	PCS		7/15			C	HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0002650	PMID:25439726	PCS		HP:0040283			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0003376	PMID:25439726	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0001762	PMID:25439726	PCS		HP:0040283			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0001288	PMID:25439726	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0003484	PMID:25439726	PCS		15/15			P	HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0012473	PMID:25439726	PCS		2/15			P	HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0012046	PMID:25439726	PCS		10/14			P	HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0007141	PMID:25439726	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0011463	PMID:25439726	PCS		8/15			C	HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0007340	PMID:25439726	PCS		15/15			P	HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0040078	PMID:25439726	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0009027	PMID:25439726	PCS					P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0000007	PMID:25439726	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0002936	PMID:25439726	PCS		4/11			P	HPO:skoehler[2015-01-28];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0003701	PMID:25439726	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0003677	PMID:25439726	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-06]
OMIM:616155	Charcot-Marie-Tooth disease, axonal, type 2S		HP:0002522	PMID:25439726	PCS		12/14			P	HPO:probinson[2023-02-06]
OMIM:618178	Nephrotic syndrome, type 19		HP:0003676	PMID:30179222	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-26]
OMIM:618178	Nephrotic syndrome, type 19		HP:0003621	PMID:30179222	PCS		2/2			C	HPO:probinson[2023-01-26]
OMIM:618178	Nephrotic syndrome, type 19		HP:0000097	PMID:30179222	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-26]
OMIM:618178	Nephrotic syndrome, type 19		HP:0000007	PMID:30179222	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-26]
OMIM:618178	Nephrotic syndrome, type 19		HP:0012625	PMID:30179222	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:618178	Nephrotic syndrome, type 19		HP:0000093	PMID:30179222	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-26]
OMIM:618178	Nephrotic syndrome, type 19		HP:0012588	PMID:30179222	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-01-26]
OMIM:277990	Intellectual disability, Wolff type		HP:0001249	OMIM:277990	IEA					P	HPO:skoehler[2015-01-27]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0030830	PMID:19760749;PMID:20502709	PCS		59/71			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002870	PMID:20502709	PCS		11/134			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0003581	PMID:17392301	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0001394	PMID:20502709	PCS		3/134			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002020	PMID:20502709	PCS		35/134			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002094	PMID:20502709	PCS		51/51			P	HPO:probinson[2020-10-07];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0012735	PMID:20502709	PCS		44/51			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0031950	PMID:20502709;PMID:17392301	PCS		34/57			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0012324	PMID:19760749	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0031413	PMID:22512499;PMID:15814878;PMID:17392301	PCS		17/17			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0045051	PMID:19760749	PCS					P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0025390	PMID:19760749	PCS					P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0100721	PMID:20502709	PCS		15/51			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0001915	PMID:15814878	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0001903	PMID:20502709	PCS		18/134			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0100759	PMID:20502709	PCS		21/51			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0000938	PMID:20502709	PCS		35/134			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0003829	PMID:17392301	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0005528	PMID:15814878	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002216	PMID:19760749	PCS		8/20			P	HPO:skoehler[2013-06-03];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002206	PMID:17392301	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002206	PMID:20502709	PCS	HP:0003581	53/134			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002206	PMID:22512499	IEA		5/5			P	HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0001876	PMID:22512499	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0000006	PMID:15814878	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-07]
OMIM:614742	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1		HP:0002863	PMID:19760749	PCS					P	HPO:probinson[2020-10-07]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002069	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000483	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000486	PMID:24738973;PMID:22693284	PCS		3/14			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-12];HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0004322	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001250	PMID:22693284	PCS		1/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000160	PMID:24738973;PMID:22693284	PCS		3/14			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-12];HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002066	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002020	PMID:22693284	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001251	PMID:22693284	PCS		6/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0003593	PMID:22693284	PCS		3/3			C	HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000718	PMID:24738973;PMID:22693284	PCS		3/14			P	HP:probinson[2022-03-12];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000316	PMID:22693284	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000752	OMIM:614756	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000358	PMID:24738973	PCS		2/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001249	PMID:24738973	PCS		2/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0005768	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002036	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000494	PMID:22693284	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001260	PMID:22693284	PCS		5/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001263	PMID:22693284	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0100540	PMID:22693284	PCS		2/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0010485	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000527	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002307	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0011170	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000369	OMIM:614756	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000006	PMID:22693284	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001611	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002003	PMID:22693284	PCS		1/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000343	PMID:22693284	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001310	PMID:22693284	PCS		5/11		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000463	PMID:22693284	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002120	OMIM:614756	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0410170	PMID:22693284	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0012450	PMID:24738973	PCS		2/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0005709	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000733	PMID:22693284	PCS		2/11			P	HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000414	PMID:24738973;PMID:22693284	PCS		11/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12];HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000337	PMID:24738973;PMID:22693284	PCS		12/13			P	HP:probinson[2022-03-12];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002317	PMID:24738973;PMID:22693284	PCS		12/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12];HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000218	PMID:24738973	PCS		2/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002714	PMID:22693284	PCS					P	HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000411	OMIM:614756	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000179	PMID:22693284	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000256	PMID:22693284	PCS		2/11			P	HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000454	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002236	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0008936	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002378	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002136	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000233	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0004279	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0002650	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000750	PMID:24738973;PMID:22693284	PCS		10/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12];HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000276	PMID:22693284	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001321	OMIM:614756	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0400005	PMID:22693284	PCS		2/11			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0007015	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000307	PMID:22693284	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0001319	PMID:22693284	PCS		3/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0007018	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000545	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:614756	Cerebellar dysfunction with variable cognitive and behavioral abnormalities		HP:0000347	PMID:24738973	PCS		1/3			P	HP:probinson[2022-03-12]
OMIM:602134	Tremor, hereditary essential, 2		HP:0007351	OMIM:602134	IEA					P	HPO:iea[2009-02-17]
OMIM:602134	Tremor, hereditary essential, 2		HP:0030186	OMIM:602134	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602134	Tremor, hereditary essential, 2		HP:0012378	OMIM:602134	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602134	Tremor, hereditary essential, 2		HP:0000006	OMIM:602134	IEA					I	HPO:iea[2009-02-17]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001276	PMID:32385911;PMID:33153867	PCS		2/3			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002421	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0000023	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001272	PMID:32385911	PCS	HP:0011462	1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001250	PMID:32385911;PMID:33153867	PCS		2/3			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002120	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001252	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0003593	PMID:32385911	PCS		1/1			C	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001270	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001508	PMID:32385911;PMID:33153867	PCS		3/3			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002119	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0000218	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0003128	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002179	PMID:32385911	PCS	HP:0003593	1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0032989	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0003202	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002059	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0000252	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002133	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0000750	PMID:33153867	PCS		2/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001662	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002098	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002151	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002490	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002092	PMID:33153867	PCS		2/2			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0011344	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0011923	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0007371	PMID:32385911	PCS	HP:0011462	1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0000007	PMID:32385911	PCS					I	HPO:probinson[2021-06-02];HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0001510	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0000047	PMID:33153867	PCS		1/1	MALE		P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002445	PMID:32385911	PCS		1/1			P	HPO:probinson[2021-06-02]
OMIM:619272	Mitochondrial complex I deficiency, nuclear type 37		HP:0002401	PMID:33153867	PCS		1/2			P	HPO:probinson[2021-06-02]
OMIM:129840	Edema, familial idiopathic, prepubertal		HP:0000819	OMIM:129840	IEA					P	HPO:iea[2009-02-17]
OMIM:129840	Edema, familial idiopathic, prepubertal		HP:0002013	OMIM:129840	IEA					P	HPO:skoehler[2010-06-20]
OMIM:129840	Edema, familial idiopathic, prepubertal		HP:0000969	OMIM:129840	IEA					P	HPO:skoehler[2010-06-20]
OMIM:129840	Edema, familial idiopathic, prepubertal		HP:0000737	OMIM:129840	IEA					P	HPO:iea[2009-02-17]
OMIM:129840	Edema, familial idiopathic, prepubertal		HP:0000119	OMIM:129840	IEA					P	HPO:iea[2009-02-17]
OMIM:129840	Edema, familial idiopathic, prepubertal		HP:0000006	OMIM:129840	IEA					I	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0001892	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0000660	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0004322	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0003077	PMID:24980439	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0003199	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0002240	PMID:24980439	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0003593	PMID:24980439	PCS		3/5			C	HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0000939	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0011463	PMID:24980439	PCS		2/5			C	HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0001943	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0002910	OMIM:232200	PCS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0001402	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0003128	PMID:24980439	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0002254	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0000991	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0000295	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0000097	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0003162	PMID:24980439	PCS		5/5			P	HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0000093	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0012213	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0000822	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0000007	PMID:24980439	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0000823	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0001538	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0001114	OMIM:232200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:232200	Glycogen storage disease Ia		HP:0001510	PMID:24980439	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:232200	Glycogen storage disease Ia		HP:0000105	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0001997	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0000787	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0001733	OMIM:232200	IEA					P	HPO:iea[2009-02-17]
OMIM:232200	Glycogen storage disease Ia		HP:0002149	PMID:24980439	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:610256	Anterior segment dysgenesis 2		HP:0007957	PMID:21150893	PCS		7/8			P	HPO:probinson[2022-09-24]
OMIM:610256	Anterior segment dysgenesis 2		HP:0003577	PMID:21150893	PCS		3/7			C	HPO:probinson[2022-09-24]
OMIM:610256	Anterior segment dysgenesis 2		HP:0007707	OMIM:610256	TAS					P	HPO:probinson[2009-02-17]
OMIM:610256	Anterior segment dysgenesis 2		HP:0007906	OMIM:610256	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000482	OMIM:610256	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000518	PMID:21150893	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000639	OMIM:610256	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610256	Anterior segment dysgenesis 2		HP:0011463	PMID:21150893	PCS		4/7			C	HPO:probinson[2022-09-24]
OMIM:610256	Anterior segment dysgenesis 2		HP:0011484	OMIM:610256	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000007	PMID:21150893	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-24]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000568	OMIM:610256	TAS					P	HPO:probinson[2009-02-17]
OMIM:610256	Anterior segment dysgenesis 2		HP:0007663	PMID:21150893	PCS		8/8			P	HPO:probinson[2022-09-24]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000659	PMID:21150893	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000526	OMIM:610256	TAS					P	HPO:probinson[2009-02-17]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000647	OMIM:610256	TAS					P	HPO:probinson[2009-02-17]
OMIM:610256	Anterior segment dysgenesis 2		HP:0000589	OMIM:610256	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610256	Anterior segment dysgenesis 2		HP:0007779	OMIM:610256	TAS					P	HPO:probinson[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000143	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0001374	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000145	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0001586	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0002023	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0002089	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0001162	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000072	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0002251	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0010741	OMIM:236700	TAS					P	HPO:probinson[2012-09-20]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000969	OMIM:236700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0030010	OMIM:236700	TAS					P	HPO:skoehler[2014-09-21]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000007	OMIM:236700	IEA					I	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0030680	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0001159	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0006159	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000113	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000028	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000126	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:236700	Mckusick-Kaufman syndrome		HP:0000148	OMIM:236700	IEA					P	HPO:iea[2009-02-17]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0003621	PMID:18523010	PCS		2/2			C	HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0001394	PMID:18523010	PCS		1/2			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0005390	PMID:18523010	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0000007	PMID:18523010	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0000029	PMID:18523010	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0005528	PMID:18523010	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0008404	PMID:18523010	PCS		2/2			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0002514	PMID:18523010	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0001510	PMID:18523010	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0001873	PMID:18523010	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0002745	PMID:18523010	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0001249	PMID:18523010	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0001876	PMID:18523010	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613987	Dyskeratosis congenita, autosomal recessive, 2		HP:0007427	PMID:18523010	PCS		1/2			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-09-25]
OMIM:233650	Combined cellular and humoral immune defects with granulomas		HP:0005403	OMIM:233650	TAS					P	HPO:probinson[2009-02-17]
OMIM:233650	Combined cellular and humoral immune defects with granulomas		HP:0005387	OMIM:233650	TAS					P	HPO:probinson[2012-07-16]
OMIM:233650	Combined cellular and humoral immune defects with granulomas		HP:0003593	OMIM:233650	IEA					C	HPO:iea[2009-02-17]
OMIM:233650	Combined cellular and humoral immune defects with granulomas		HP:0000007	OMIM:233650	IEA					I	HPO:iea[2009-02-17]
OMIM:233650	Combined cellular and humoral immune defects with granulomas		HP:0002205	OMIM:233650	IEA					P	HPO:iea[2009-02-17]
OMIM:233650	Combined cellular and humoral immune defects with granulomas		HP:0010976	OMIM:233650	TAS					P	HPO:probinson[2012-07-16]
OMIM:233650	Combined cellular and humoral immune defects with granulomas		HP:0004315	OMIM:233650	TAS					P	HPO:probinson[2009-02-17]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001276	PMID:31495489	PCS		9/15			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000286	PMID:31495489	PCS		5/21			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000341	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000340	PMID:31495489	PCS		4/21			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0010804	PMID:31495489	PCS		3/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0002365	PMID:31495489	PCS		3/20			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0002002	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001250	PMID:31495489	PCS		10/17			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0011913	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001252	PMID:31495489	PCS		4/15			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0012745	PMID:31495489	PCS		4/21			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000819	PMID:31495489	PCS		2/19			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000319	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000954	PMID:31495489	PCS		1/21		HP:0012832	P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000414	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000219	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0003429	PMID:31495489	PCS		7/19			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001522	PMID:31495489	PCS		6/18			C	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000411	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0006610	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000358	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001622	PMID:31495489	PCS		7/18			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000253	PMID:31495489	PCS		9/10			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0002553	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000252	PMID:31495489	PCS		15/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000494	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000233	PMID:31495489	IEA		3/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001321	PMID:31495489	PCS		10/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0003561	PMID:31495489	PCS		6/11			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000193	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001263	PMID:31495489	PCS		7/7			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000470	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000294	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001181	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0005280	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0100336	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001838	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000007	PMID:31495489	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0002804	PMID:31495489	PCS	HP:0003577	17/20			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0002804	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000601	PMID:31495489	PCS		1/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0001511	PMID:31495489	PCS	HP:0011461	12/19			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000322	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0002643	PMID:31495489	PCS	HP:0003623	14/17			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0000303	PMID:31495489	PCS		2/21			P	HPO:probinson[2020-06-27]
OMIM:618622	Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies		HP:0009879	PMID:31495489	PCS		12/18			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:612469	WAGRO syndrome		HP:0002762	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000341	PMID:11807873	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0003577	PMID:11807873;PMID:15702131	PCS		3/3			C	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0007957	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0010529	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000518	PMID:11807873;PMID:15702131	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000718	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000739	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000712	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000678	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000713	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0008734	PMID:11807873	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0001249	PMID:11807873;PMID:15702131	PCS		3/3			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000494	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0012815	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0007906	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0002591	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000272	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000093	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0012760	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000729	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000508	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000822	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000744	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000722	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000505	PMID:15702131	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000526	PMID:11807873;PMID:15702131	PCS		3/3			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0002667	PMID:11807873;PMID:15702131	PCS		2/3			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000006	PMID:18753648	PCS					I	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000666	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000369	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000303	PMID:11807873	PCS		1/1			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0000347	PMID:15702131	PCS		1/2			P	HPO:probinson[2022-08-07]
OMIM:612469	WAGRO syndrome		HP:0001513	PMID:15702131	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:605115	Hypertension, early-onset, autosomal dominant, with severe exacerbationin pregnancy		HP:0003351	OMIM:605115	TAS					P	HPO:probinson[2013-02-23]
OMIM:605115	Hypertension, early-onset, autosomal dominant, with severe exacerbationin pregnancy		HP:0000822	OMIM:605115	TAS					P	HPO:probinson[2013-01-09]
OMIM:605115	Hypertension, early-onset, autosomal dominant, with severe exacerbationin pregnancy		HP:0004319	OMIM:605115	TAS					P	HPO:probinson[2013-02-23]
OMIM:605115	Hypertension, early-onset, autosomal dominant, with severe exacerbationin pregnancy		HP:0000006	OMIM:605115	TAS					I	HPO:probinson[2013-02-23]
OMIM:605115	Hypertension, early-onset, autosomal dominant, with severe exacerbationin pregnancy		HP:0008071	PMID:10884226	PCS					H	HPO:probinson[2013-02-23]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0003236	OMIM:261670	IEA					P	HPO:iea[2009-02-17]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0003201	OMIM:261670	IEA					P	HPO:skoehler[2010-06-18]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0003198	OMIM:261670	IEA					P	HPO:iea[2009-02-17]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0000083	OMIM:261670	IEA					P	HPO:iea[2009-02-17]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0002913	OMIM:261670	IEA					P	HPO:iea[2009-02-17]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0003738	OMIM:261670	IEA					P	HPO:iea[2009-02-17]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0000007	OMIM:261670	IEA					I	HPO:iea[2009-02-17]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0003710	OMIM:261670	IEA					P	HPO:iea[2009-02-17]
OMIM:261670	Phosphoglycerate mutase, muscle, deficiency of		HP:0003546	OMIM:261670	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0002069	PMID:21549339	PCS		3/6			P	HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0003236	PMID:21549339	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0003676	PMID:21549339	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0002650	PMID:21549339	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0001288	PMID:21549339	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0002354	PMID:21549339	PCS		2/6			P	HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0001761	PMID:21549339	PCS		1/6			P	HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0002121	PMID:21549339	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0010819	PMID:21549339	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0001260	OMIM:614018	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0001284	PMID:21549339	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0001251	PMID:21549339	PCS	HP:0011463	6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0010850	PMID:21549339	PCS		4/6			P	HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0032667	PMID:21549339	PCS		1/6			P	HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0011463	PMID:21549339	PCS		6/6			C	HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0000007	PMID:21549339	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0002505	PMID:21549339	PCS	HP:0003621	6/6			P	HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0001337	PMID:21549339	PCS		2/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-09-25]
OMIM:614018	Epilepsy, progressive myoclonic, 6		HP:0001336	PMID:21549339	PCS		6/6			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-09-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0002960	PMID:22289921	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0002202	PMID:19425169	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0020072	PMID:22289921;PMID:21109689	PCS		5/5			P	HPO:probinson[2020-11-25];HPO:probinson[2020-11-25];HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001890	PMID:22289921	PCS		1/2			P	HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0002240	PMID:19425169	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0012156	PMID:19425169	PCS		0/2			P	HPO:skoehler[2013-06-10];HPO:probinson[2020-10-13];HPO:probinson[2024-03-14]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0002719	PMID:21109689	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001903	PMID:19425169	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0011463	PMID:21109689	PCS		3/3			C	HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0002716	PMID:22289921;PMID:19425169	PCS		4/4			P	HPO:probinson[2020-11-25];HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0012191	PMID:22289921	PCS		1/2			P	HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001744	PMID:19425169	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0004315	PMID:21109689	PCS		2/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0003565	PMID:19425169	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0003621	PMID:22289921;PMID:19425169	PCS		4/4			C	HPO:probinson[2020-11-25];HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0004313	PMID:22289921;PMID:19425169	PCS		2/4			P	HPO:probinson[2020-11-25];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0005523	PMID:22289921	PCS		1/2			P	HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001882	PMID:22289921	PCS		2/2			P	HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0003281	PMID:19425169	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0011227	PMID:19425169	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0012189	PMID:19425169;PMID:21109689	PCS		4/5		HP:0033185	P	HPO:probinson[2020-11-25];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0010280	PMID:19425169	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0000007	PMID:19425169	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001954	PMID:22289921;PMID:19425169	PCS		4/4			P	HPO:probinson[2020-11-25];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001698	PMID:19425169	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001973	PMID:22289921	PCS		1/2			P	HPO:probinson[2020-11-25]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001873	PMID:19425169	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-13]
OMIM:613011	Lymphoproliferative syndrome 1		HP:0001876	PMID:19425169	PCS		1/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-10-13]
OMIM:217080	Jalili syndrome		HP:0000670	PMID:19200527	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0007803	OMIM:217080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:217080	Jalili syndrome		HP:0007814	PMID:19200527	PCS		2/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0007737	PMID:19200527	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000662	PMID:19200527	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0003593	PMID:19200527	PCS					C	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0033785	PMID:19200527	PCS		6/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000639	PMID:19200527	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0012043	PMID:19200527	PCS		2/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0006286	PMID:19200527	PCS		6/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000613	PMID:19200527	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0008499	PMID:19200527	PCS		2/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000007	PMID:19200527	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000505	PMID:19200527	PCS		6/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000548	OMIM:217080	IEA					P	HPO:iea[2009-02-17]
OMIM:217080	Jalili syndrome		HP:0007401	PMID:19200527	PCS		3/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000543	PMID:19200527	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0007843	PMID:19200527	PCS		3/6			P	HPO:probinson[2022-10-23]
OMIM:217080	Jalili syndrome		HP:0000575	PMID:19200527	PCS		1/6			P	HPO:probinson[2022-10-23]
OMIM:609049	Pierson syndrome		HP:0003774	PMID:15367484	PCS	HP:0003593	13/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0003774	PMID:17256789	PCS		4/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0003577	PMID:17256789	IEA		4/4			C	HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000541	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000100	PMID:15367484	PCS	HP:0003623				P	HPO:probinson[2009-02-17];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0000100	PMID:17256789	PCS		4/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0003075	OMIM:609049	IEA					P	HPO:iea[2009-02-17]
OMIM:609049	Pierson syndrome		HP:0001252	PMID:15372515;PMID:17256789	PCS		5/19			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-14];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0001270	PMID:17256789	PCS		3/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0012841	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000518	PMID:17256789	PCS		3/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000618	PMID:15372515	PCS		1/15			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0004719	PMID:17256789	PCS		4/4			P	HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000558	PMID:15367484	IEA		1/15			P	HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0001967	PMID:15367484	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0025358	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0001104	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0003623	PMID:15367484	PCS					C	HPO:probinson[2009-02-17];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0001265	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0001562	PMID:17256789	PCS	HP:0011461	2/4			P	HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000253	PMID:17256789	PCS		2/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0003202	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000252	PMID:17256789	PCS		3/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0007968	PMID:17256789	PCS		3/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000573	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0011968	PMID:17256789	PCS		2/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0001263	PMID:15367484;PMID:17256789	PCS		4/19			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20];HPO:skoehler[2019-09-07];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0001284	PMID:17256789	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0033454	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000093	PMID:17256789	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0011003	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0025492	PMID:15367484;PMID:17256789	PCS		6/19			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-14];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0032988	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0011502	PMID:15372515	PCS					P	HPO:probinson[2012-07-26];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0003819	PMID:17256789	PCS		2/4			C	HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000969	PMID:17256789	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000822	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000007	PMID:15367484	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0007894	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0000568	PMID:17256789	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:609049	Pierson syndrome		HP:0007774	PMID:15372515	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-10-14]
OMIM:609049	Pierson syndrome		HP:0007676	PMID:15372515	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-10-14]
OMIM:618144	Usher syndrome, type IV		HP:0001133	PMID:32455177	PCS		1/1			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0007737	PMID:32455177;PMID:29300381	PCS		6/6			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0001751	PMID:29300381	PCS		0/5			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0000662	PMID:32455177	PCS		1/1			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0030631	PMID:32455177	PCS		1/1			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0000408	PMID:29300381	PCS	HP:0003596	5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0000407	PMID:32455177	PCS		1/1			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0000007	PMID:29300381	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0000546	PMID:32455177	PCS		1/1			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0030529	PMID:29300381	PCS		5/5			P	HPO:probinson[2021-06-26]
OMIM:618144	Usher syndrome, type IV		HP:0001105	PMID:29300381	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-26]
OMIM:618150	Saul-Wilson syndrome		HP:0003015	PMID:30290151	PCS		13/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0003577	PMID:30290151	PCS		14/14			C	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000662	PMID:30290151	PCS		6/9			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000365	PMID:30290151	PCS		11/14			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0004322	PMID:30290151	PCS		14/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0003311	PMID:30290151	PCS		13/13			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000260	PMID:30290151	PCS		12/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0003396	PMID:30290151	PCS		1/4			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0010049	PMID:30290151	PCS		13/13			P	HPO:skoehler[2019-02-15]
OMIM:618150	Saul-Wilson syndrome		HP:0001270	PMID:30290151	PCS		12/14			P	HPO:skoehler[2019-02-15]
OMIM:618150	Saul-Wilson syndrome		HP:0010743	PMID:30290151	PCS		13/13			P	HPO:skoehler[2019-02-15]
OMIM:618150	Saul-Wilson syndrome		HP:0006391	PMID:30290151	PCS		13/13			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000518	PMID:30290151	PCS		11/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0010230	PMID:30290151	PCS		12/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0011220	PMID:30290151	PCS		14/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0009882	PMID:30290151	PCS		12/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0008897	PMID:30290151	PCS		14/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0002119	PMID:30290151	PCS		5/10			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0005328	PMID:30290151	PCS		8/14			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0003301	PMID:30290151	PCS		11/13			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000750	PMID:30290151	PCS		8/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0001762	PMID:30290151	PCS		10/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0002673	PMID:30290151	PCS		13/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0003067	PMID:30290151	PCS		5/13			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0002176	PMID:30290151	PCS		3/7			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000592	PMID:30290151	PCS		9/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0001263	PMID:30290151	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0009193	PMID:30290151	PCS		11/12			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0010580	PMID:30290151	PCS		13/13			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000407	PMID:30290151	PCS		2/14			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000926	PMID:30290151	PCS		7/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000767	PMID:30290151	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0006442	PMID:30290151	PCS		9/11			P	HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000768	PMID:30290151	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000444	PMID:30290151	PCS		6/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0001511	PMID:30290151	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0001015	PMID:30290151	PCS		14/14			P	HPO:skoehler[2019-02-15]
OMIM:618150	Saul-Wilson syndrome		HP:0000520	PMID:30290151	PCS		13/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000006	PMID:30290151	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000347	PMID:30290151	PCS		12/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0000446	PMID:30290151	PCS		8/14			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618150	Saul-Wilson syndrome		HP:0001875	PMID:30290151	PCS		11/14			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:613005	Santos syndrome		HP:0100259	OMIM:613005	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613005	Santos syndrome		HP:0012165	OMIM:613005	TAS					P	HPO:skoehler[2013-02-25]
OMIM:613005	Santos syndrome		HP:0001762	OMIM:613005	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613005	Santos syndrome		HP:0001156	OMIM:613005	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613005	Santos syndrome		HP:0004322	OMIM:613005	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613005	Santos syndrome		HP:0100258	OMIM:613005	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613005	Santos syndrome		HP:0002857	OMIM:613005	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613005	Santos syndrome		HP:0010442	OMIM:613005	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613005	Santos syndrome		HP:0001159	OMIM:613005	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613005	Santos syndrome		HP:0001840	OMIM:613005	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613005	Santos syndrome		HP:0000006	PMID:19012338	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-10]
OMIM:613005	Santos syndrome		HP:0001798	OMIM:613005	IEA					P	HPO:skoehler[2010-06-19]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0002069	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0002510	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0003577	PMID:23913001	PCS		2/2			C	HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0200128	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0011706	PMID:23913001	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0001263	PMID:23913001	PCS		2/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0003351	PMID:23913001	PCS		2/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0032794	PMID:23913001	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0100021	PMID:23913001	PCS		2/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0002092	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0011736	PMID:23913001	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0001629	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0100704	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0200114	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0000822	PMID:23913001	PCS	HP:0003623	2/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0001712	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0002900	PMID:23913001	PCS		2/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0001257	PMID:23913001	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0002305	PMID:23913001	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0000787	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0001249	PMID:23913001	PCS		1/2			P	HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0000006	PMID:23913001	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615474	Primary aldosteronism, seizures, and neurologic abnormalities		HP:0001655	PMID:23913001	PCS		1/2			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-10-24]
OMIM:615312	Albinism, oculocutaneous, type V		HP:0001022	OMIM:615312	IEA					P	HPO:skoehler[2015-01-27]
OMIM:615312	Albinism, oculocutaneous, type V		HP:0000639	OMIM:615312	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615312	Albinism, oculocutaneous, type V		HP:0007750	OMIM:615312	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615312	Albinism, oculocutaneous, type V		HP:0000613	OMIM:615312	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615312	Albinism, oculocutaneous, type V		HP:0000007	OMIM:615312	TAS					I	HPO:skoehler[2014-01-28]
OMIM:613763	Cataract 16, multiple types		HP:0003577	PMID:11577372	PCS		16/16			C	HPO:probinson[2022-11-06]
OMIM:613763	Cataract 16, multiple types		HP:0001142	PMID:11577372	PCS		0/16			P	HPO:probinson[2022-11-06]
OMIM:613763	Cataract 16, multiple types		HP:0000519	PMID:11577372	PCS		HP:0040283			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-11-06]
OMIM:613763	Cataract 16, multiple types		HP:0000007	PMID:11577372	PCS					I	HPO:skoehler[2013-06-06];HPO:probinson[2022-11-06]
OMIM:613763	Cataract 16, multiple types		HP:0011003	PMID:11577372	PCS		0/16			P	HPO:probinson[2022-11-06]
OMIM:613763	Cataract 16, multiple types		HP:0001115	PMID:11577372	PCS	HP:0003577	16/16			P	HPO:probinson[2013-06-05];HPO:probinson[2022-11-06]
OMIM:613763	Cataract 16, multiple types		HP:0000006	PMID:11577372	PCS					I	HPO:probinson[2013-06-05];HPO:probinson[2022-11-06]
OMIM:613763	Cataract 16, multiple types		HP:0000556	OMIM:613763	TAS		HP:0040283			P	HPO:skoehler[2013-06-06]
OMIM:177900	Psoriasis 1, susceptibility to		HP:0025088	OMIM:177900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:177900	Psoriasis 1, susceptibility to		HP:0001806	OMIM:177900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:177900	Psoriasis 1, susceptibility to		HP:0001426	OMIM:177900	TAS					I	HPO:iea[2009-02-17]
OMIM:177900	Psoriasis 1, susceptibility to		HP:0001803	OMIM:177900	TAS					P	HPO:iea[2009-02-17]
OMIM:177900	Psoriasis 1, susceptibility to		HP:0003765	OMIM:177900	TAS					P	HPO:iea[2009-02-17]
OMIM:177900	Psoriasis 1, susceptibility to		HP:0001369	OMIM:177900	PCS					P	HPO:iea[2009-02-17]
OMIM:601367	Ischemic stroke, susceptibility to		HP:0001297	PMID:20042462	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-06-17]
OMIM:601367	Ischemic stroke, susceptibility to		HP:0003581	PMID:20042462	PCS					C	HPO:probinson[2022-06-01]
OMIM:601367	Ischemic stroke, susceptibility to		HP:0001426	PMID:20042462	PCS					I	HPO:probinson[2020-06-17]
OMIM:619528	Spermatogenic failure 57		HP:0003251	PMID:34347949	PCS		4/4			P	HPO:probinson[2021-10-23]
OMIM:619528	Spermatogenic failure 57		HP:0011462	PMID:34347949	PCS		4/4			C	HPO:probinson[2021-10-23]
OMIM:619528	Spermatogenic failure 57		HP:0000007	PMID:34347949	PCS					I	HPO:probinson[2021-10-23];HPO:probinson[2021-10-23]
OMIM:619528	Spermatogenic failure 57		HP:0031038	PMID:34347949	PCS		4/4			P	HPO:probinson[2021-10-23]
OMIM:619528	Spermatogenic failure 57		HP:0008734	PMID:34347949	PCS		4/4			P	HPO:probinson[2021-10-23]
OMIM:619528	Spermatogenic failure 57		HP:0011961	PMID:34347949	PCS		4/4			P	HPO:probinson[2021-10-23]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0002036	OMIM:606408	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000076	OMIM:606408	TAS					P	HPO:skoehler[2012-11-21]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0003555	OMIM:606408	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0001058	PMID:11642233	PCS		0/8			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000122	OMIM:606408	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0001382	PMID:11642233	PCS		8/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000061	OMIM:606408	TAS					P	HPO:skoehler[2012-11-21]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0001065	PMID:11642233	PCS		1/8			P	HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0001075	PMID:11642233	PCS		0/8			P	HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0031655	OMIM:606408	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0002829	OMIM:606408	IEA					P	HPO:skoehler[2010-06-19]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0032153	OMIM:606408;PMID:11642233	PCS		12/18		HP:0031796	P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0009025	OMIM:606408	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000007	PMID:11642233	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000978	PMID:11642233	PCS		8/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000813	OMIM:606408	TAS					P	HPO:skoehler[2012-11-21]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000977	PMID:11642233	PCS		7/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0007126	OMIM:606408	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0003701	OMIM:606408	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0000974	PMID:11642233	PCS		8/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-10]
OMIM:606408	Ehlers-Danlos syndrome, classic-like		HP:0001634	OMIM:606408	TAS					P	HPO:skoehler[2012-11-21]
OMIM:168820	Paraoxonase 1		HP:0001939	OMIM:168820	IEA					P	HPO:iea[2009-02-17]
OMIM:168820	Paraoxonase 1		HP:0000006	OMIM:168820	IEA					I	HPO:iea[2009-02-17]
OMIM:611174	Hamamy syndrome		HP:0045075	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0011343	PMID:22581230	PCS		4/4			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000319	PMID:34899143;PMID:22581230	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0011220	PMID:34899143	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000316	PMID:22581230	PCS		5/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0100807	OMIM:611174	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611174	Hamamy syndrome		HP:0200021	PMID:34899143;PMID:22581230	PCS		9/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0006677	PMID:34899143;PMID:22581230	PCS		4/6			P	HPO:probinson[2022-09-04]
OMIM:611174	Hamamy syndrome		HP:0001249	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001385	PMID:22581230	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001263	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0010511	PMID:22581230	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001182	PMID:22581230	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0011003	PMID:22581230	PCS		3/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000407	PMID:22581230	PCS		4/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000767	PMID:22581230	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000689	PMID:22581230	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000007	PMID:22581230	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001935	PMID:22581230	PCS		4/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0004209	PMID:22581230	PCS		2/5			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0009536	OMIM:611174	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611174	Hamamy syndrome		HP:0001653	PMID:22581230	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000369	PMID:34899143;PMID:22581230	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001931	PMID:22581230	PCS		4/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000248	PMID:34899143;PMID:22581230	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0005338	PMID:22581230	PCS		5/5			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000384	PMID:22581230	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0003577	PMID:34899143	PCS		2/2			C	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000343	PMID:22581230	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001674	PMID:22581230	PCS		1/5			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000023	PMID:22581230	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000463	PMID:22581230	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0002162	PMID:22581230	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000581	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0008070	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0012371	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000938	PMID:34899143;PMID:22581230	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0006297	PMID:34899143;PMID:22581230	PCS		5/5			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000219	PMID:34899143;PMID:22581230	PCS		6/7			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0002757	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000218	PMID:22581230	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000653	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000154	PMID:34899143;PMID:22581230	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001363	PMID:22581230	PCS		3/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000431	PMID:34899143;PMID:22581230	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0010813	PMID:22581230	PCS		5/5			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000232	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000829	PMID:22581230	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000506	PMID:34899143	PCS		2/2			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000668	PMID:22581230	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001159	PMID:22581230	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0001631	PMID:22581230	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0009759	PMID:34899143;PMID:22581230	PCS		5/7			P	HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000347	PMID:22581230	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-21]
OMIM:611174	Hamamy syndrome		HP:0000028	PMID:34899143;PMID:22581230	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:616394	Retinitis pigmentosa 71		HP:0000662	PMID:25168386	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:616394	Retinitis pigmentosa 71		HP:0002650	PMID:25168386	PCS		1/2			P	HPO:probinson[2021-10-20]
OMIM:616394	Retinitis pigmentosa 71		HP:0012426	PMID:25168386	PCS		2/2			P	HPO:probinson[2021-10-20]
OMIM:616394	Retinitis pigmentosa 71		HP:0000007	PMID:25168386	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-20]
OMIM:616394	Retinitis pigmentosa 71		HP:0030629	PMID:25168386	PCS		2/2			P	HPO:probinson[2021-10-20];HPO:probinson[2021-10-20]
OMIM:616394	Retinitis pigmentosa 71		HP:0000543	PMID:25168386	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2021-10-20]
OMIM:616394	Retinitis pigmentosa 71		HP:0000510	PMID:25168386	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-20]
OMIM:616394	Retinitis pigmentosa 71		HP:0007843	PMID:25168386	PCS		1/1			P	HPO:skoehler[2015-06-22];HPO:probinson[2021-10-20]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0001561	OMIM:300073	IEA					P	HPO:iea[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0002375	OMIM:300073	IEA					P	HPO:iea[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0000506	OMIM:300073	IEA					P	HPO:iea[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0000581	OMIM:300073	IEA					P	HPO:iea[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0001274	OMIM:300073	IEA					P	HPO:iea[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0003826	OMIM:300073	IEA					C	HPO:iea[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0045025	OMIM:300073	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0001417	OMIM:300073	IEA					I	HPO:iea[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0001989	OMIM:300073	TAS					P	HPO:probinson[2009-02-17]
OMIM:300073	Fetal akinesia syndrome, X-linked		HP:0002139	OMIM:300073	IEA					P	HPO:iea[2009-02-17]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000365	OMIM:614583	TAS		5/6			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000343	OMIM:614583	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0004322	OMIM:614583	TAS		3/7			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000243	OMIM:614583	TAS		7/7			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0001250	OMIM:614583	TAS		7/8			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0001274	OMIM:614583	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000316	OMIM:614583	TAS		7/8			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0030680	OMIM:614583	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000637	OMIM:614583	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000219	OMIM:614583	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0002119	OMIM:614583	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0001302	OMIM:614583	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000377	OMIM:614583	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000278	OMIM:614583	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0001249	OMIM:614583	TAS		5/5			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0002553	OMIM:614583	TAS		7/7			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000154	OMIM:614583	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0005484	OMIM:614583	TAS		4/7			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000470	OMIM:614583	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000506	OMIM:614583	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000508	OMIM:614583	TAS		8/8			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0001339	OMIM:614583	TAS		7/7			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000568	OMIM:614583	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000307	OMIM:614583	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000202	OMIM:614583	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000465	OMIM:614583	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000589	OMIM:614583	TAS		5/7			P	HPO:probinson[2013-08-10]
OMIM:614583	Baraitser-Winter syndrome 2		HP:0000006	OMIM:614583	TAS		5/7			I	HPO:probinson[2013-08-10]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0000541	OMIM:219250	TAS	HP:0003577				P	HPO:skoehler[2013-04-01]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0006385	OMIM:219250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0000822	OMIM:219250	IEA					P	HPO:iea[2009-02-17]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0000965	OMIM:219250	IEA					P	HPO:iea[2009-02-17]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0001009	OMIM:219250	IEA					P	HPO:iea[2009-02-17]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0002979	OMIM:219250	IEA					P	HPO:iea[2009-02-17]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0000007	OMIM:219250	IEA					I	HPO:iea[2009-02-17]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0025107	OMIM:219250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0000501	OMIM:219250	TAS					P	HPO:skoehler[2010-06-20]
OMIM:219250	Cutis marmorata telangiectatica congenita		HP:0000555	OMIM:219250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:620154	Oocyte maturation defect 13		HP:0008222	PMID:34611029	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:620154	Oocyte maturation defect 13		HP:0011462	PMID:34611029	PCS		2/2			C	HPO:probinson[2023-03-04]
OMIM:620154	Oocyte maturation defect 13		HP:0000007	PMID:34611029	PCS					I	HPO:probinson[2023-03-04]
OMIM:620154	Oocyte maturation defect 13		HP:0033712	PMID:34611029	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:159800	Myoclonus, cerebellar ataxia, and deafness		HP:0000365	OMIM:159800	IEA					P	HPO:iea[2009-02-17]
OMIM:159800	Myoclonus, cerebellar ataxia, and deafness		HP:0001251	OMIM:159800	IEA					P	HPO:iea[2009-02-17]
OMIM:159800	Myoclonus, cerebellar ataxia, and deafness		HP:0000006	OMIM:159800	IEA					I	HPO:iea[2009-02-17]
OMIM:159800	Myoclonus, cerebellar ataxia, and deafness		HP:0001336	OMIM:159800	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0004322	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000040	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0001263	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0003074	OMIM:262190	IEA					P	HPO:skoehler[2010-06-20]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0003162	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0011998	OMIM:262190	TAS					P	HPO:skoehler[2015-12-30]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000280	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0012542	OMIM:262190	TAS					P	HPO:probinson[2013-12-15]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000826	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000958	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0001518	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000998	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000007	OMIM:262190	IEA					I	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0001943	OMIM:262190	IEA					P	HPO:skoehler[2010-06-20]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0006288	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000956	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0008665	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000218	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000303	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000831	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0000842	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities		HP:0001953	OMIM:262190	IEA					P	HPO:iea[2009-02-17]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0001034	PMID:29336782	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0003621	PMID:29336782	PCS		6/9			C	HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0020073	PMID:29336782	PCS		9/9			P	HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0000992	PMID:29336782	PCS		0/9			P	HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0000958	PMID:29336782	PCS		9/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0011463	PMID:29336782	PCS		3/9			C	HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0007440	PMID:29336782	PCS		9/9			P	HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0000007	PMID:29336782	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-09]
OMIM:617920	Amyloidosis, primary localized cutaneous, 3		HP:0000989	PMID:29336782	PCS		2/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-09]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0000033	OMIM:608800	IEA					P	HPO:iea[2009-02-17]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0002267	PMID:15273283	PCS		21/21			P	HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0008715	OMIM:608800	IEA					P	HPO:iea[2009-02-17]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0002793	OMIM:608800	IEA					P	HPO:iea[2009-02-17]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0002045	PMID:15273283	PCS	HP:0003593				P	HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0001662	PMID:15273283	PCS	HP:0003593				P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0010307	OMIM:608800	TAS					P	HPO:skoehler[2010-06-18]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0008708	OMIM:608800	IEA					P	HPO:iea[2009-02-17]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0002020	PMID:15273283	PCS	HP:0003593			HP:0012828	P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0025431	OMIM:608800	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0003593	PMID:15273283	PCS					C	HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0001608	OMIM:608800	IEA					P	HPO:iea[2009-02-17]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0000007	PMID:15273283	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0008872	PMID:15273283	PCS	HP:0003593	21/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0025425	PMID:15273283	PCS	HP:0003593				P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0001308	PMID:15273283	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0006543	PMID:15273283	PCS	HP:0003593				P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0008733	PMID:15273283	PCS			MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0001510	OMIM:608800	IEA					P	HPO:iea[2009-02-17]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0002104	OMIM:608800	IEA					P	HPO:iea[2009-02-17]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:4000007	PMID:15273283	PCS	HP:0003593				P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0000028	PMID:15273283	PCS			MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0001699	PMID:15273283	PCS	HP:0003593				P	HPO:probinson[2022-11-04]
OMIM:608800	Sudden infant death with dysgenesis of the testes syndrome		HP:0003623	PMID:15273283	PCS					C	HPO:probinson[2022-11-04]
OMIM:114900	Carcinoid tumors, intestinal		HP:0000006	OMIM:114900	IEA					I	HPO:iea[2009-02-17]
OMIM:114900	Carcinoid tumors, intestinal		HP:0006723	OMIM:114900	IEA					P	HPO:iea[2009-02-17]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000286	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001276	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000341	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0003676	PMID:24577744	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000486	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0004322	PMID:24577744	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001272	PMID:30100179;PMID:24577744	PCS		12/12		HP:0003676	P	HPO:probinson[2020-12-13];HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001371	PMID:24577744	PCS	HP:0003621				P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0003196	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0003593	PMID:30100179;PMID:24577744	PCS		12/12			C	HPO:probinson[2020-12-13];HPO:skoehler[2015-12-30];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0032794	PMID:24577744	PCS					P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0012469	PMID:30100179	PCS	HP:0003593	2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0007380	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000939	PMID:24577744	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001508	PMID:30100179	PCS		1/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000737	PMID:24577744	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0002119	PMID:30100179	PCS		1/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001249	PMID:24577744	PCS		10/10		HP:0012829	P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0009748	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0002179	PMID:24577744	PCS		10/10			P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000253	PMID:24577744	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0002059	PMID:30100179;PMID:24577744	PCS		12/12		HP:0003676	P	HPO:probinson[2020-12-13];HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000252	PMID:24577744	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0002510	PMID:24577744	PCS		10/10		HP:0003676	P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0002650	PMID:24577744	PCS	HP:0003621				P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0002079	PMID:24577744	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001263	PMID:30100179;PMID:24577744	PCS		12/12		HP:0012828	P	HPO:probinson[2020-12-13];HPO:skoehler[2014-06-24];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0005484	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0025190	PMID:24577744	PCS	HP:0011463	10/10			P	HPO:probinson[2020-12-13];HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0011344	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0032792	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000007	PMID:24577744	PCS					I	HPO:probinson[2021-02-05]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001319	OMIM:615851	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000648	PMID:30100179	PCS		1/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001257	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000347	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0001336	PMID:30100179	PCS	HP:0003593	1/2			P	HPO:probinson[2020-12-13]
OMIM:615851	Pontocerebellar hypoplasia, type 2E		HP:0000445	PMID:30100179	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0003593	PMID:30936877	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0003073	PMID:26008899	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0012548	PMID:26008899	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0032435	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0031402	PMID:30936877;PMID:26008899	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0040081	PMID:30936877;PMID:26008899	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0032183	PMID:30936877;PMID:26008899	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0001903	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0033351	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0007340	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0002718	PMID:30936877	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0008897	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0410305	PMID:26008899	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0200043	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0001744	PMID:30936877;PMID:26008899	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0031190	PMID:30936877	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0004315	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0003623	PMID:26008899	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0410301	PMID:30936877;PMID:26008899	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0005403	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0003202	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0003565	PMID:26008899	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0020180	PMID:26008899	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0002254	PMID:26008899	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0002593	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0001263	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0011227	PMID:26008899	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0001954	PMID:30936877;PMID:26008899	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0000964	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0001217	PMID:30936877;PMID:26008899	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0000007	PMID:26008899	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0004429	PMID:30936877	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620632	Immunodeficiency 115 with autoinflammation		HP:0002721	PMID:30936877;PMID:26008899	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0008936	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0000054	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001250	OMIM:300067	PCS					P	HPO:iea[2012-03-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001260	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001274	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001251	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0003593	OMIM:300067	TAS					C	HPO:skoehler[2012-10-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0031882	OMIM:300067	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0002282	OMIM:300067	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001270	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0000639	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0003829	OMIM:300067	IEA					I	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001339	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0008897	OMIM:300067	PCS					P	HPO:iea[2012-03-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001417	OMIM:300067	IEA					I	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001302	OMIM:300067	IEA					P	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001522	OMIM:300067	IEA					C	HPO:iea[2009-02-17]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001257	OMIM:300067	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300067	Lissencephaly, X-linked, 1		HP:0001249	OMIM:300067	PCS					P	HPO:iea[2012-03-17]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000286	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0003577	PMID:27991732	PCS		1/1			C	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0010803	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0002002	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000463	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0004684	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001250	PMID:24614070	PCS		2/13			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0004442	PMID:24614070	PCS		1/13			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0002263	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0002000	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001252	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000581	OMIM:615879	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001629	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0040197	OMIM:615879	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001548	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000316	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0002119	PMID:24614070	PCS		1/13			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001528	PMID:24614070	PCS		1/13		HP:0012825	P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0025116	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000311	PMID:27991732;PMID:24614070	PCS		11/11			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-05-10];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000256	PMID:24614070	PCS		7/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001249	PMID:24614070	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000076	PMID:24614070	PCS		1/13			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000098	PMID:24614070	PCS		11/13			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000233	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000574	PMID:24614070	PCS					P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0002650	PMID:24614070	PCS		4/13			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0002373	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001263	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0045025	PMID:27991732;PMID:24614070	PCS		11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-10];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0010499	PMID:24614070	PCS		1/13			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0005180	PMID:24614070	PCS		1/13			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0011228	PMID:27991732	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000609	OMIM:615879	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0007099	PMID:27991732	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001537	PMID:27991732;PMID:24614070	PCS		3/14			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-05-10];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001653	PMID:24614070	PCS		1/13			P	HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0001631	PMID:24614070	PCS		2/13			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-05-10]
OMIM:615879	Tatton-Brown-Rahman syndrome		HP:0000006	PMID:24614070	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-10]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000286	OMIM:162100	IEA					P	HPO:iea[2009-02-17]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0001265	OMIM:162100	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0003202	OMIM:162100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000175	OMIM:162100	IEA					P	HPO:iea[2009-02-17]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000582	OMIM:162100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0004322	OMIM:162100	IEA					P	HPO:iea[2009-02-17]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000160	OMIM:162100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000490	OMIM:162100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000581	OMIM:162100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0045054	PMID:16186812	PCS					P	HPO:skoehler[2015-09-25];HPO:probinson[2020-10-13]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0005280	OMIM:162100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0033142	OMIM:162100	TAS					P	HPO:probinson[2020-10-13]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000508	OMIM:162100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0040078	OMIM:162100	TAS					P	HPO:skoehler[2014-11-26]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0009830	OMIM:162100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000601	OMIM:162100	IEA					P	HPO:iea[2009-02-17]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0001324	OMIM:162100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000006	PMID:16186812	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000369	OMIM:162100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000324	OMIM:162100	IEA					P	HPO:iea[2009-02-17]
OMIM:162100	Amyotrophy, hereditary neuralgic		HP:0000764	OMIM:162100	IEA					P	HPO:iea[2009-02-17]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0004325	PMID:39088281	PCS		0/9			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000286	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0002664	PMID:39088281	PCS		0/9			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000365	PMID:39088281	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0004322	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000162	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0012471	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000717	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0040012	PMID:39088281	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0005528	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0009625	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000278	PMID:39088281	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0009626	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000175	PMID:39088281	PCS		2/7			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:5201016	PMID:39088281	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000331	PMID:39088281	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000407	PMID:39088281	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000767	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0009777	PMID:39088281	PCS		2/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0004209	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000201	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001972	PMID:39088281	PCS		4/9			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0009778	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000325	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000369	PMID:39088281	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000006	PMID:39088281	PCS					I	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0025802	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0003577	PMID:39088281	PCS		10/10			C	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000023	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0031688	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001909	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001508	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001903	PMID:39088281	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0032188	PMID:39088281	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0008551	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001943	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000218	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001945	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0006610	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000413	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001864	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0002013	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001882	PMID:39088281	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0004871	PMID:39088281	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000272	PMID:39088281	PCS		6/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:6000942	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000348	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0009237	PMID:39088281	PCS		5/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0005518	PMID:39088281	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0007018	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001873	PMID:39088281	PCS		3/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0000347	PMID:39088281	PCS		5/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001876	PMID:39088281	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:621262	Diamond-Blackfan anemia 22		HP:0001875	PMID:39088281	PCS		4/10			P	ORCID:0000-0002-0736-9199[2025-10-18]
OMIM:166400	Osteomas of mandible		HP:0000277	OMIM:166400	IEA					P	HPO:iea[2009-02-17]
OMIM:166400	Osteomas of mandible		HP:0100246	OMIM:166400	IEA					P	HPO:skoehler[2015-01-27]
OMIM:166400	Osteomas of mandible		HP:0000006	OMIM:166400	IEA					I	HPO:iea[2009-02-17]
OMIM:143870	Hypercalciuria, absorptive, susceptibility to		HP:0008672	OMIM:143870	TAS					P	HPO:skoehler[2009-02-17]
OMIM:143870	Hypercalciuria, absorptive, susceptibility to		HP:0002150	OMIM:143870	TAS					P	HPO:skoehler[2010-06-18]
OMIM:143870	Hypercalciuria, absorptive, susceptibility to		HP:0000006	PMID:11932268	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2021-06-21]
OMIM:218600	Baller-Gerold syndrome		HP:0000286	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0003510	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000483	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0002023	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000244	PMID:15964893	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000486	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0004443	PMID:15964893	PCS		1/6			P	HPO:iea[2012-02-24];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0004322	PMID:15964893	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0004442	OMIM:218600	IEA					P	HPO:iea[2012-02-24]
OMIM:218600	Baller-Gerold syndrome		HP:0001250	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000160	PMID:15964893	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0004440	PMID:15964893	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0003031	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0010048	OMIM:218600	TAS					P	HPO:probinson[2012-05-01]
OMIM:218600	Baller-Gerold syndrome		HP:0011341	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0011220	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000316	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000239	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000238	PMID:15964893	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0009821	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0009702	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0003468	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0001249	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000358	OMIM:218600	TAS					P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000175	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000494	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0004334	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0002870	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000452	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0011968	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0011003	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000609	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0034197	PMID:15964893	PCS		2/6			C	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0034198	PMID:15964893	PCS		1/6			C	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0002308	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000007	PMID:15964893	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0009777	PMID:15964893	PCS		3/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000648	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000405	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0006467	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000248	PMID:15964893	PCS		2/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0002984	PMID:15964893	PCS		2/6			P	HPO:probinson[2012-06-03];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0008846	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000369	OMIM:218600	TAS					P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000143	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0003577	PMID:15964893	PCS		1/6			C	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000263	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000260	PMID:15964893	PCS		3/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0003298	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0001274	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000262	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0005792	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0001270	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0010783	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0011318	PMID:1583650	PCS					P	HPO:probinson[2015-03-01]
OMIM:218600	Baller-Gerold syndrome		HP:0011120	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0009486	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0030680	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0001627	OMIM:218600	TAS					P	HPO:skoehler[2015-12-30]
OMIM:218600	Baller-Gerold syndrome		HP:0000218	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000410	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0001029	PMID:15964893	PCS		2/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0001545	PMID:15964893	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0002996	PMID:15964893	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000077	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0005886	OMIM:218600	IEA					P	HPO:probinson[2012-05-01]
OMIM:218600	Baller-Gerold syndrome		HP:0001363	PMID:15964893	PCS		4/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0002650	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000233	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000430	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0005201	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0003022	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0004871	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000193	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0004231	OMIM:218600	TAS					P	HPO:probinson[2012-05-01]
OMIM:218600	Baller-Gerold syndrome		HP:0003065	PMID:15964893	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0012165	PMID:15964893	PCS		3/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000902	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0007452	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0000426	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0006443	PMID:15964893	PCS		1/6			P	HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0003974	PMID:15964893	PCS		1/6			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000347	PMID:15964893	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:218600	Baller-Gerold syndrome		HP:0000545	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0002126	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:218600	Baller-Gerold syndrome		HP:0004425	OMIM:218600	IEA					P	HPO:iea[2009-02-17]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0003730	PMID:34938096	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-26]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0002015	OMIM:255700	TAS					P	HPO:probinson[2010-06-18]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0008968	OMIM:255700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0003621	PMID:18337100	PCS					C	HPO:probinson[2022-07-19]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0003552	PMID:18337100	PCS		25/27			P	HPO:probinson[2012-04-27]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0002486	PMID:34938096	PCS		2/2			P	HPO:probinson[2012-04-27];HPO:probinson[2022-06-26]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0003740	PMID:18337100;PMID:34938096	PCS		29/29			P	HPO:probinson[2022-06-26];HPO:probinson[2012-04-27];HPO:probinson[2022-06-26]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0010548	PMID:18337100	PCS		26/27			P	HPO:probinson[2010-06-18]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0011463	PMID:18337100;PMID:34938096	PCS		12/12			C	HPO:probinson[2022-07-19];HPO:probinson[2012-04-27];HPO:probinson[2022-06-26]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0011462	PMID:18337100	PCS					C	HPO:probinson[2022-07-19]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0000007	PMID:1379744	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-26]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0001324	PMID:34938096	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-06-26]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0003712	PMID:18337100;PMID:34938096	PCS		17/29			P	HPO:probinson[2022-06-26];HPO:probinson[2012-04-27];HPO:probinson[2022-06-26]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0025605	PMID:18337100	PCS		7/27			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-19]
OMIM:255700	Myotonia congenita, autosomal recessive		HP:0003326	PMID:18337100;PMID:34938096	PCS		13/29			P	HPO:probinson[2022-06-26];HPO:probinson[2012-04-27];HPO:probinson[2022-06-26]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0001344	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-03]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0011968	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-08]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0001250	PMID:35675825	PCS	HP:0003593	1/1			P	HPO:probinson[2022-08-08]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0003593	PMID:35675825	PCS		1/1			C	HPO:probinson[2022-08-08]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0010862	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-08]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0010465	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-03]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0011182	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-03]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0012450	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-08]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0000007	PMID:35675825	PCS					I	HPO:probinson[2022-08-03]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0100716	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-03]
OMIM:619931	Intellectual developmental disorder, autosomal recessive 76		HP:0020049	PMID:35675825	PCS		1/1			P	HPO:probinson[2022-08-03]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002982	PMID:17277775	PCS	HP:0011461				P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002980	PMID:17277775	PCS	HP:0011461				P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000023	PMID:17277775	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0001552	PMID:17277775	PCS		1/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000260	PMID:17277775	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0005474	PMID:17277775	PCS		2/4			P	HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0010049	PMID:17277775	PCS	HP:0011463	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000938	PMID:17277775	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0011461	PMID:17277775	PCS		5/5			C	HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0008796	PMID:17277775	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0008873	PMID:17277775	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002757	PMID:17277775	PCS	HP:0011461	5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002953	PMID:17277775	PCS	HP:0011463	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000311	PMID:17277775	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002650	PMID:17277775	PCS	HP:0003621	1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0003784	PMID:17277775	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0001382	PMID:17277775	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0003100	PMID:17277775	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0004331	PMID:17277775	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0001263	PMID:17277775	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002808	PMID:17277775	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000926	PMID:17277775	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000007	PMID:17277775	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000703	PMID:17277775	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002645	PMID:17277775	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0002986	PMID:17277775	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000520	PMID:17277775	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0000883	PMID:17277775	PCS	HP:0011461	5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:610915	Osteogenesis imperfecta, type VIII		HP:0005855	PMID:17277775	PCS	HP:0011461	5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-17]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0003577	PMID:12046007	PCS		7/7			C	HPO:probinson[2023-03-12]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0004322	OMIM:251200	TAS	HP:0003593	HP:0040283			P	HPO:iea[2009-02-17]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0001250	PMID:12046007	PCS		0/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0002472	OMIM:251200	IEA					P	HPO:iea[2009-02-17]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0003451	OMIM:251200	IEA					P	HPO:iea[2009-02-17]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0011451	PMID:12046007	PCS		7/7			P	HPO:probinson[2023-03-12]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0000007	PMID:12046007	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:251200	Microcephaly, primary autosomal recessive, 1		HP:0001249	PMID:12046007	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0002487	PMID:12555939	PCS		1/2			P	HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001276	PMID:12555939	PCS		1/2			P	HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001254	OMIM:236270	IEA					P	HPO:iea[2009-02-17]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0002120	PMID:12555939	PCS		1/2			P	HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001250	PMID:12555939	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001252	PMID:12555939	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0003593	OMIM:236270	TAS					C	HPO:skoehler[2013-10-06]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0002160	PMID:12555939	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001508	PMID:12555939	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0000639	PMID:12555939	PCS		1/2			P	HPO:skoehler[2013-10-06]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0000618	OMIM:236270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001889	PMID:12555939	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0002912	PMID:12555939	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0003524	OMIM:236270	IEA					P	HPO:iea[2009-02-17]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0003623	PMID:12555939	PCS		2/2			C	HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0002059	OMIM:236270	TAS					P	HPO:skoehler[2013-10-06]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0003223	OMIM:236270	IEA					P	HPO:iea[2009-02-17]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001288	OMIM:236270	TAS					P	HPO:skoehler[2013-10-06]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0002156	OMIM:236270	IEA					P	HPO:iea[2009-02-17]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001263	PMID:12555939	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0012120	PMID:12555939	PCS		0/2			P	HPO:skoehler[2013-05-30];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0000007	PMID:9501215	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0003658	PMID:12555939	PCS		1/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-05]
OMIM:236270	Homocystinuria-megaloblastic anemia, cbl E type		HP:0001897	PMID:12555939	PCS		2/2			P	HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0003577	PMID:26888176	PCS		1/4			C	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0031956	PMID:26888176	PCS		4/4			P	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0002202	PMID:26888176	PCS	HP:0003577	1/4			P	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001399	PMID:26888176	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001541	PMID:26888176	PCS	HP:0003577	1/4			P	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001394	PMID:26888176	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0003593	PMID:26888176	PCS		1/4			C	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001790	PMID:26888176	PCS	HP:0011461	1/4			P	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0031964	PMID:26888176	PCS		4/4			P	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0002908	PMID:26888176	PCS		4/4			P	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0008151	PMID:26888176	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001508	PMID:26888176	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0006254	PMID:26888176	PCS		4/4			P	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0000007	PMID:26888176	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001987	PMID:26888176	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001943	PMID:26888176	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0001522	PMID:26888176	PCS		2/4			C	HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0000952	PMID:26888176	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0003678	PMID:26888176	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:617049	Cholestasis, progressive familial intrahepatic, 5		HP:0003623	PMID:26888176	PCS		2/4			C	HPO:probinson[2021-10-03]
OMIM:616357	Deafness, autosomal dominant 40		HP:0001751	PMID:12471561	PCS		0/3			P	HPO:probinson[2017-06-14];HPO:probinson[2024-03-15]
OMIM:616357	Deafness, autosomal dominant 40		HP:0000407	PMID:12471561	PCS		3/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2024-03-15]
OMIM:616357	Deafness, autosomal dominant 40		HP:0011463	PMID:12471561	PCS		3/3			C	HPO:probinson[2024-03-15]
OMIM:616357	Deafness, autosomal dominant 40		HP:0000006	PMID:12471561	PCS					I	HPO:skoehler[2015-09-16]
OMIM:616357	Deafness, autosomal dominant 40		HP:0001249	PMID:12471561	PCS		0/3			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0001254	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0003577	PMID:28247525	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0001531	PMID:28247525	PCS					P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0001640	PMID:28247525	PCS					P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0000260	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0000490	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0002151	PMID:28247525	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0001252	PMID:28247525	PCS					P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0002240	PMID:28247525	PCS					P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0003593	PMID:28247525	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0002092	PMID:28247525	PCS		2/2			P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0003819	PMID:28247525	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0000007	PMID:28247525	PCS					I	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0000527	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0008347	PMID:28247525	PCS					P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0008358	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0002007	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0000664	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0001522	PMID:28247525	PCS		1/2			C	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0002910	PMID:28247525	PCS		2/2			P	HPO:probinson[2020-12-08];HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0001348	PMID:28247525	PCS					P	HPO:probinson[2020-12-08]
OMIM:619064	Mitochondrial complex IV deficiency, nuclear type 20		HP:0003348	PMID:28247525	PCS		1/2			P	HPO:probinson[2020-12-08]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0003577	PMID:34903892	PCS		21/21			C	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001696	PMID:34903892	PCS		8/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001674	PMID:34903892	PCS		7/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001651	PMID:34903892	PCS		6/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001750	PMID:34903892	PCS		4/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0011556	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0004383	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0031565	PMID:34903892	PCS		5/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0011553	PMID:34903892	PCS		2/21			P	HPO:probinson[2022-02-24];HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0031348	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0012304	PMID:34903892	PCS		2/21			P	HPO:probinson[2022-02-24];HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001629	PMID:34903892	PCS		3/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0011640	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0011540	PMID:34903892	PCS		3/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0004935	PMID:34903892	PCS		3/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001643	PMID:34903892	PCS		5/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001642	PMID:34903892	PCS		4/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001680	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0010773	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0011565	PMID:34903892	PCS		2/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0031854	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0011590	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001719	PMID:34903892	PCS		7/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0012020	PMID:34903892	PCS		1/21			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0011670	PMID:34903892	PCS		3/42			P	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0000007	PMID:34903892	PCS					I	HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001631	PMID:34903892	PCS		5/21			P	HPO:probinson[2022-02-24];HPO:probinson[2022-02-24]
OMIM:619702	Heterotaxy, visceral, 12, autosomal		HP:0001655	PMID:34903892	PCS		2/21			P	HPO:probinson[2022-02-24]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000286	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0003577	PMID:35044816	PCS		2/2			C	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0001684	PMID:35044816	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000452	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000023	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0002120	PMID:35044816	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000185	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0009909	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0010880	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000957	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0011451	PMID:35044816	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000007	PMID:35044816	PCS					I	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000637	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000219	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000956	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0002119	PMID:35044816	PCS		1/1			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0025116	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0004209	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0001511	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0002777	PMID:35044816	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0000201	PMID:35044816	PCS		1/2			P	HPO:probinson[2023-03-25]
OMIM:620183	Microcephaly 30, primary, autosomal recessive		HP:0001249	PMID:35044816	PCS		1/1			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
DECIPHER:44	2q37 monosomy		HP:0001156	DECIPHER:44	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:44	2q37 monosomy		HP:0000490	DECIPHER:44	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:44	2q37 monosomy		HP:0000219	DECIPHER:44	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:44	2q37 monosomy		HP:0000311	DECIPHER:44	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:44	2q37 monosomy		HP:0001249	DECIPHER:44	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614226	Holoprosencephaly 11		HP:0000252	PMID:21802063	PCS					P	HPO:probinson[2013-03-12]
OMIM:614226	Holoprosencephaly 11		HP:0000175	OMIM:614226	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614226	Holoprosencephaly 11		HP:0000574	OMIM:614226	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614226	Holoprosencephaly 11		HP:0001360	PMID:21802063	PCS					P	HPO:probinson[2013-01-09]
OMIM:614226	Holoprosencephaly 11		HP:0001274	PMID:21802063	PCS					P	HPO:probinson[2013-03-12]
OMIM:614226	Holoprosencephaly 11		HP:0001263	PMID:21802063	PCS					P	HPO:probinson[2013-03-12]
OMIM:614226	Holoprosencephaly 11		HP:0410030	OMIM:614226	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614226	Holoprosencephaly 11		HP:0003828	OMIM:614226	TAS					M	HPO:skoehler[2017-07-13]
OMIM:614226	Holoprosencephaly 11		HP:0000601	PMID:21802063	PCS					P	HPO:probinson[2013-03-12]
OMIM:614226	Holoprosencephaly 11		HP:0001748	OMIM:614226	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614226	Holoprosencephaly 11		HP:0000664	PMID:21802063	PCS					P	HPO:probinson[2013-03-12]
OMIM:614226	Holoprosencephaly 11		HP:0003745	OMIM:614226	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614226	Holoprosencephaly 11		HP:0000520	OMIM:614226	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614226	Holoprosencephaly 11		HP:0000006	PMID:21802063	PCS					I	HPO:probinson[2013-03-12]
OMIM:612657	Cone-rod dystrophy 12		HP:0000662	PMID:26702251	PCS					P	HPO:probinson[2020-07-17]
OMIM:612657	Cone-rod dystrophy 12		HP:0000551	PMID:26702251	PCS					P	HPO:probinson[2020-07-17]
OMIM:612657	Cone-rod dystrophy 12		HP:0008323	PMID:26702251	PCS					P	HPO:probinson[2020-07-17]
OMIM:612657	Cone-rod dystrophy 12		HP:0007663	PMID:18654668	PCS					P	HPO:probinson[2015-07-20]
OMIM:612657	Cone-rod dystrophy 12		HP:0000007	PMID:26702251	PCS					I	HPO:probinson[2020-07-17]
OMIM:612657	Cone-rod dystrophy 12		HP:0000548	PMID:18654668	PCS					P	HPO:probinson[2013-04-06]
OMIM:612657	Cone-rod dystrophy 12		HP:0000603	PMID:26702251	PCS					P	HPO:probinson[2020-07-17]
OMIM:612657	Cone-rod dystrophy 12		HP:0011504	PMID:26702251	PCS					P	HPO:probinson[2020-07-17]
OMIM:612657	Cone-rod dystrophy 12		HP:0000006	PMID:18654668	PCS					I	HPO:probinson[2013-01-09]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0005359	OMIM:602450	TAS					P	HPO:probinson[2012-07-20]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0003212	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0003593	PMID:15731174;PMID:34220820	PCS		2/2			C	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0002240	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0030813	OMIM:602450	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0031545	PMID:34220820	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0001508	PMID:15731174;PMID:34220820	PCS		2/2			P	HPO:probinson[2022-05-26];HPO:iea[2009-02-17];HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0100806	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0001888	PMID:34220820	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0001744	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0002732	OMIM:602450	IEA					P	HPO:iea[2009-02-17]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0003249	OMIM:602450	IEA					P	HPO:iea[2009-02-17]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0001880	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0000155	OMIM:602450	IEA					P	HPO:iea[2009-02-17]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0020086	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0004430	PMID:15731174	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0002293	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0002090	OMIM:602450	IEA					P	HPO:iea[2009-02-17]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0010976	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0030350	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0000007	PMID:15731174	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0008940	PMID:15731174	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0002788	OMIM:602450	IEA					P	HPO:iea[2009-02-17]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0000388	OMIM:602450	IEA					P	HPO:iea[2009-02-17]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0003139	OMIM:602450	IEA					P	HPO:iea[2009-02-17]
OMIM:602450	Severe combined immunodeficiency with sensitivity to ionizing radiation		HP:0002028	PMID:34220820	PCS		1/1			P	HPO:probinson[2022-05-26]
OMIM:612643	Deafness, autosomal dominant 3B		HP:0000006	OMIM:612643	TAS					I	HPO:probinson[2013-01-09]
OMIM:612643	Deafness, autosomal dominant 3B		HP:0008615	OMIM:612643	TAS					P	HPO:probinson[2013-04-14]
OMIM:616425	46,XY sex reversal 10		HP:0008715	PMID:22051515	PCS		2/5			P	HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000054	PMID:22051515	PCS					P	HPO:skoehler[2015-07-05];HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000046	PMID:22051515	PCS		1/5			P	HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000133	PMID:22051515	PCS		2/5			P	HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000051	PMID:22051515	PCS		2/5			P	HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000150	PMID:22051515	PCS		1/5			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000062	PMID:22051515	PCS		HP:0040283			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0012245	PMID:22051515	PCS		5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0012861	PMID:22051515	PCS		4/5			P	HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0100621	OMIM:616425	TAS					P	HPO:skoehler[2015-07-05]
OMIM:616425	46,XY sex reversal 10		HP:0008734	PMID:22051515	PCS		HP:0040283			P	HPO:skoehler[2015-07-05];HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000048	PMID:22051515	PCS		1/5			P	HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000047	PMID:22051515	PCS		1/5			P	HPO:probinson[2022-12-20]
OMIM:616425	46,XY sex reversal 10		HP:0000006	PMID:22051515	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-20]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0001696	PMID:36047773	PCS		0/3			P	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0002110	PMID:32555313;PMID:36047773	PCS		12/12			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0003251	PMID:32555313	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0033036	PMID:36047773	PCS		0/3			P	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0100582	PMID:36047773	PCS					P	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0034315	PMID:32555313	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0011108	PMID:32555313	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0032559	PMID:32555313	PCS		2/2			P	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0012265	PMID:32555313	PCS		2/2			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0032560	PMID:32555313	PCS		2/2			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0011463	PMID:36047773	PCS		3/3			C	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0000007	PMID:32555313	PCS					I	HPO:probinson[2023-06-11]
OMIM:620197	Ciliary dyskinesia, primary, 49, without situs inversus		HP:0002205	PMID:36047773	PCS		3/3			P	HPO:probinson[2023-06-11]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0001012	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000286	OMIM:181270	TAS		2/17			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0011939	OMIM:181270	TAS					P	HPO:probinson[2009-02-17]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0004322	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000089	PMID:23541344	PCS		4/15			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0001057	PMID:23541344	PCS		29/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000122	PMID:23541344	PCS		1/15			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000083	PMID:23541344	PCS		5/15			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0006709	PMID:23541344	PCS		21/26			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000958	PMID:23541344	PCS		2/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000518	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000519	OMIM:181270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000358	PMID:23541344	PCS		1/12			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0004755	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0002215	PMID:23541344	PCS		9/9			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0002232	PMID:23541344	PCS		1/12			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0004691	OMIM:181270	IEA					P	HPO:iea[2009-02-17]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0100783	OMIM:181270	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0100540	OMIM:181270	TAS					P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0011251	PMID:23541344	PCS		1/12			P	HPO:iea[2011-12-18];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000601	OMIM:181270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0006101	PMID:23541344	PCS		6/19			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000966	PMID:23541344	PCS		6/7			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0004209	PMID:23541344	PCS		3/19			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0002225	PMID:23541344	PCS		9/9			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000369	PMID:23541344	PCS		2/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000006	PMID:23541344	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0006349	OMIM:181270	TAS					P	HPO:iea[2009-02-17]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000385	OMIM:181270	IEA					P	HPO:iea[2011-12-18]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000463	OMIM:181270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0009916	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0002164	PMID:23541344	PCS		11/20			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0002000	OMIM:181270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000581	OMIM:181270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0001072	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0040080	PMID:23541344	PCS		8/14			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0008070	OMIM:181270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0012330	PMID:23541344	PCS		1/15			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0008551	PMID:23541344	PCS		3/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000612	OMIM:181270	TAS		1/17			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000411	OMIM:181270	IEA					P	HPO:iea[2009-02-17]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000378	OMIM:181270	IEA					P	HPO:iea[2009-02-17]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000652	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000396	PMID:23541344	PCS		16/19			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0006956	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0002213	PMID:23541344	PCS		7/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000992	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000193	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0001362	PMID:23541344	PCS		2/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0045025	OMIM:181270	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0005280	OMIM:181270	TAS		3/17			P	HPO:skoehler[2013-10-06]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0011304	PMID:23541344	PCS		1/19			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0011272	PMID:23541344	PCS		1/12			P	HPO:iea[2011-12-18];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000506	PMID:23541344	PCS		5/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0011672	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000822	OMIM:181270	TAS		7/17			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0001635	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0002007	PMID:23541344	PCS		1/17			P	HPO:probinson[2023-03-15]
OMIM:181270	Scalp-ear-nipple syndrome		HP:0000303	OMIM:181270	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0003015	OMIM:187601	TAS					P	HPO:probinson[2015-03-21]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0002983	PMID:28249712	PCS	HP:0030674	5/5			P	HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0001156	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0008909	OMIM:187601	TAS					P	HPO:probinson[2012-05-01]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0034222	PMID:28249712	PCS		1/5			P	HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0000910	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0002119	PMID:28249712	PCS		1/5			P	HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0000774	PMID:28249712	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0000773	PMID:28249712	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0002676	PMID:28249712	PCS		5/5		HP:0012828	P	HPO:probinson[2012-05-01];HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0002677	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0000274	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0001561	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0003025	OMIM:187601	TAS					P	HPO:probinson[2015-03-21]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0001321	PMID:28249712	PCS		1/5			P	HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0003185	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0002093	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0034199	PMID:28249712	PCS		1/5			C	HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0034198	PMID:28249712	PCS		4/5			C	HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0000946	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0000926	PMID:28249712	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0006584	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0001558	OMIM:187601	IEA					P	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0003811	OMIM:187601	IEA					C	HPO:iea[2009-02-17]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0002007	PMID:28249712	PCS		5/5			P	HPO:probinson[2023-06-10]
OMIM:187601	Thanatophoric dysplasia, type II		HP:0000006	PMID:7773297	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-10]
OMIM:615892	Orofacial cleft 14		HP:0000161	PMID:23519333	PCS					P	HP:probinson[2019-03-02]
OMIM:615892	Orofacial cleft 14		HP:0000007	PMID:23860042	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0004325	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001276	PMID:26416026	PCS		2/2			P	HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0003577	PMID:26416026	PCS		2/2			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0010804	PMID:26416026	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0004322	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001371	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001250	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0009085	PMID:26416026	PCS		2/2			P	HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001508	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0009748	PMID:26416026	PCS		1/2			P	HPO:probinson[2022-04-08];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001348	PMID:26416026	PCS		2/2			P	HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0000252	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001344	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0002353	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0002133	PMID:26416026	PCS	HP:0003593	1/2			P	HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0012736	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0005280	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001518	PMID:26416026	PCS	HP:0003577	2/2			P	HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0000007	PMID:26416026	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0000348	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001338	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0000648	PMID:26416026	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001511	PMID:26416026	PCS	HP:0011461	2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0000520	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0000322	PMID:26416026	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:618346	Microcephaly, growth deficiency, seizures, and brain malformations		HP:0001257	PMID:26416026	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-08]
OMIM:617075	Nasopharyngeal carcinoma, susceptibility to, 3		HP:0100630	PMID:26951679	PCS	HP:0011462	7/13			P	HPO:probinson[2019-04-20]
OMIM:617075	Nasopharyngeal carcinoma, susceptibility to, 3		HP:0000006	OMIM:617075	TAS					I	HPO:skoehler[2017-07-13]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0000286	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0100543	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0004322	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0007141	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0000490	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0001263	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0000007	PMID:25604084	PCS					I	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0008347	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0001513	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0003688	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:619058	Mitochondrial complex IV deficiency, nuclear type 14		HP:0003546	PMID:25604084	PCS		1/1			P	HPO:probinson[2020-12-06];HPO:probinson[2020-12-06]
OMIM:613575	Retinitis pigmentosa 55		HP:0000007	PMID:19956407	PCS					I	HPO:probinson[2013-01-09]
OMIM:613575	Retinitis pigmentosa 55		HP:0000510	PMID:19956407	PCS					P	HPO:probinson[2013-02-18]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0006208	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0003016	PMID:12554676	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0002980	PMID:12554676	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0006429	PMID:16088909	PCS		7/7			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0004322	PMID:16088909	PCS		9/10			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0005871	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0003371	PMID:16088909	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0011463	PMID:12554676;PMID:16088909	PCS		8/8			C	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0009882	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0002938	PMID:12554676;PMID:16088909	PCS		3/8			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0006431	OMIM:156500	IEA					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0003508	PMID:12554676	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0002812	PMID:16088909	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0002515	PMID:12554676	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0004979	PMID:12554676	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0002857	PMID:16088909	PCS		2/6			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0008833	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0009844	OMIM:156500	TAS					P	HPO:skoehler[2013-04-13]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0006414	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0003502	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0003301	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0002650	PMID:16088909	PCS		1/7			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0002970	PMID:12554676;PMID:16088909	PCS		5/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-23];HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0003025	PMID:12554676	PCS		1/1			P	HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0000926	PMID:16088909	PCS		0/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-23]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0005819	OMIM:156500	TAS					P	HPO:skoehler[2013-04-13]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0006028	OMIM:156500	TAS					P	HPO:probinson[2009-02-17]
OMIM:156500	Metaphyseal chondrodysplasia, Schmid type		HP:0000006	PMID:8220429	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-23]
OMIM:618420	Spermatogenic failure 36		HP:0003251	PMID:30893644	TAS		4/4			P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2022-09-04]
OMIM:618420	Spermatogenic failure 36		HP:0011462	PMID:30893644	PCS		4/4			C	HPO:probinson[2022-09-04]
OMIM:618420	Spermatogenic failure 36		HP:0000006	PMID:30893644	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-04]
OMIM:618420	Spermatogenic failure 36		HP:0012864	PMID:30893644	TAS		3/3			P	HPO:nvasilevsky[2019-09-11];HPO:probinson[2022-09-04]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000483	PMID:28942965	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003236	PMID:28942965	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003577	PMID:28942965	PCS		1/4			C	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000100	PMID:28942965	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0001695	PMID:28942965	PCS		1/4			P	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003198	PMID:28942965	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0002240	PMID:28942965	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0002181	PMID:28942965	PCS		1/4			P	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0002910	PMID:28942965	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003546	PMID:28942965	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003623	PMID:28942965	PCS		1/4			C	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003128	PMID:28942965	PCS		2/4			P	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0001562	PMID:28942965	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003621	PMID:28942965	PCS		1/4			C	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0001640	PMID:28942965	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000590	PMID:28942965	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0011924	PMID:28942965	PCS		4/4			P	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0003584	PMID:28942965	PCS		1/4			C	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0002151	PMID:28942965	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0010851	PMID:28942965	PCS		1/2			P	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0011923	PMID:28942965	PCS		4/4			P	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0012378	PMID:28942965	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000407	PMID:28942965	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000508	PMID:28942965	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000646	PMID:28942965	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000007	PMID:28942965	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0000821	PMID:28942965	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0001712	PMID:28942965	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0001638	PMID:28942965	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0008347	PMID:28942965	PCS		4/4			P	HPO:probinson[2023-06-06]
OMIM:617713	Combined oxidative phosphorylation deficiency 33		HP:0001511	PMID:28942965	PCS		1/4			P	HPO:probinson[2023-06-06]
OMIM:611376	Mungan syndrome		HP:0000076	OMIM:611376	TAS					P	HPO:probinson[2009-02-17]
OMIM:611376	Mungan syndrome		HP:0030996	PMID:25575569	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0004389	PMID:25575569	PCS		3/3			P	HPO:probinson[2012-07-18];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0000089	OMIM:611376	IEA					P	HPO:probinson[2009-02-17]
OMIM:611376	Mungan syndrome		HP:0002270	OMIM:611376	TAS					P	HPO:probinson[2012-07-18]
OMIM:611376	Mungan syndrome		HP:0100580	PMID:25575569	PCS		3/3			P	HPO:probinson[2012-07-18];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0005180	PMID:25575569	PCS		1/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0100771	PMID:25575569	PCS		3/3			P	HPO:probinson[2012-07-18];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0011682	PMID:25575569	PCS		1/3			P	HPO:probinson[2012-07-18];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0000007	PMID:25575569	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0001642	PMID:25575569	PCS		2/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0001488	PMID:25575569	PCS		1/3			P	HPO:probinson[2012-07-18];HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0002027	PMID:25575569	PCS		3/3			P	HPO:probinson[2022-10-03]
OMIM:611376	Mungan syndrome		HP:0002578	PMID:25575569	PCS		3/3			P	HPO:probinson[2022-10-03]
OMIM:618434	Deafness, autosomal recessive 94		HP:0008619	PMID:25807530	PCS	HP:0003593	4/4		HP:0012829	P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618434	Deafness, autosomal recessive 94		HP:0001751	OMIM:618434	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618434	Deafness, autosomal recessive 94		HP:0000007	PMID:25807530	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:617707	Spermatogenic failure 23		HP:0003251	PMID:28206990	PCS		2/2			P	HPO:probinson[2023-03-17]
OMIM:617707	Spermatogenic failure 23		HP:0011462	PMID:28206990	PCS		2/2			C	HPO:probinson[2023-03-17]
OMIM:617707	Spermatogenic failure 23		HP:0000007	PMID:28206990	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-17]
OMIM:617707	Spermatogenic failure 23		HP:0000027	PMID:28206990	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-17]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0003323	PMID:15372378	PCS					P	HPO:probinson[2013-03-05]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0003202	PMID:15372378	PCS					P	HPO:probinson[2013-03-05]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002015	PMID:15372378	PCS		11/16			P	HPO:probinson[2013-03-05];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0003596	PMID:15372378	PCS		8/16			C	HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002483	PMID:15372378	PCS		12/16			P	HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0003693	PMID:15372378	PCS		7/16			P	HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0001260	OMIM:608627	TAS					P	HPO:skoehler[2015-08-16]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0003394	PMID:15372378	PCS		15/16			P	HPO:probinson[2013-03-05];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0001284	PMID:15372378	PCS					P	HPO:probinson[2013-03-05]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002460	PMID:15372378	PCS		9/16			P	HPO:probinson[2013-03-05];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002174	PMID:15372378	PCS		16/16			P	HPO:probinson[2013-03-05];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002380	PMID:15372378	PCS		15/16			P	HPO:probinson[2013-03-05];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002062	PMID:15372378	PCS					P	HPO:probinson[2013-03-05]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0100543	PMID:15372378	PCS		0/16			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0011462	PMID:15372378	PCS		8/16			C	HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0007354	PMID:15372378	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002529	PMID:15372378	PCS					P	HPO:probinson[2013-01-09]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0007256	PMID:15372378	PCS		5/16			P	HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0002505	PMID:15372378	PCS		5/16			P	HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0007126	PMID:15372378	PCS		10/16			P	HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0003701	PMID:15372378	PCS		13/16			P	HPO:probinson[2013-03-05];HPO:probinson[2022-08-08]
OMIM:608627	Amyotrophic lateral sclerosis 8		HP:0000006	PMID:15372378	PCS					I	HPO:probinson[2013-03-05]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001254	PMID:20598274	PCS		2/3			P	HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0003676	PMID:20598274	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0000486	OMIM:613561	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0000980	PMID:20598274	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001252	PMID:20598274	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0002240	OMIM:613561	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0003593	PMID:20598274	PCS		3/3			C	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001270	PMID:20598274	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001508	PMID:20598274	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0000639	OMIM:613561	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001924	PMID:20598274	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001324	PMID:20598274	PCS		2/3			P	HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0002910	OMIM:613561	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0003688	PMID:20598274	PCS		1/1			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0003546	PMID:20598274	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0003700	OMIM:613561	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0003128	PMID:20598274	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0002015	PMID:20598274	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0003200	PMID:20598274	PCS		1/1			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0002098	PMID:20598274	PCS		1/3			P	HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0011924	PMID:20598274	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0002151	PMID:20598274	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0011923	PMID:20598274	PCS		3/3			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001639	PMID:20598274	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0000508	OMIM:613561	TAS					P	HPO:skoehler[2014-02-25]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0000007	PMID:20598274	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0008347	PMID:20598274	PCS		3/3			P	HPO:probinson[2023-02-17];HPO:probinson[2023-02-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0002747	OMIM:613561	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613561	Myopathy, lactic acidosis, and sideroblastic anemia 2		HP:0001510	OMIM:613561	TAS					P	HPO:skoehler[2012-10-17]
OMIM:144110	Hyperhidrosis palmaris et plantaris		HP:0007410	OMIM:144110	IEA					P	HPO:iea[2009-02-17]
OMIM:144110	Hyperhidrosis palmaris et plantaris		HP:0000006	OMIM:144110	IEA					I	HPO:iea[2009-02-17]
OMIM:612119	Trehalase deficiency		HP:0002014	OMIM:612119	TAS					P	HPO:probinson[2012-07-21]
OMIM:612119	Trehalase deficiency		HP:0000007	OMIM:612119	TAS					I	HPO:probinson[2012-07-21]
OMIM:612119	Trehalase deficiency		HP:0002027	OMIM:612119	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618352	Central centrifugal cicatricial alopecia		HP:0004552	OMIM:618352	TAS					P	HPO:probinson[2020-08-02]
OMIM:618352	Central centrifugal cicatricial alopecia		HP:0000006	OMIM:618352	IEA					I	HPO:skoehler[2019-04-18]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000286	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0002465	PMID:32109419	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001250	PMID:32109419	PCS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001252	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0003196	PMID:32109419	PCS		1/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0003593	PMID:32109419	PCS		15/15			C	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0011463	PMID:26721934	PCS		4/4			C	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000718	PMID:32109419	PCS		5/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0012471	PMID:26721934	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000316	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000954	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000678	PMID:26721934	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001643	PMID:32109419	PCS	HP:0003623	1/4			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000278	PMID:32109419	PCS		2/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001007	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001249	PMID:26721934;PMID:32109419	PCS		19/19			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000677	PMID:32109419	PCS		1/15			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000494	PMID:26721934	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000252	PMID:26721934;PMID:32109419	PCS		13/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000574	PMID:26721934	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000331	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0011968	PMID:26721934;PMID:32109419	PCS		10/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000294	PMID:32109419	PCS		2/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0004691	PMID:32109419	PCS		1/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0011800	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001182	PMID:26721934;PMID:32109419	PCS		9/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0012378	PMID:26721934	PCS		3/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000729	PMID:26721934	PCS		2/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000767	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000722	PMID:32109419	PCS		3/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0004209	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000400	PMID:26721934	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001852	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000322	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000006	PMID:26721934	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001337	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000324	PMID:26721934;PMID:32109419	PCS		4/18			P	HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000582	PMID:32109419	PCS		2/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000343	PMID:26721934;PMID:32109419	PCS		2/18			P	HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001156	PMID:26721934	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0003691	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001270	PMID:26721934	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0002719	PMID:26721934	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001629	PMID:32109419	PCS	HP:0003577	1/4			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0007021	PMID:32109419	PCS		2/10			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0012450	PMID:26721934;PMID:32109419	PCS		7/16			P	HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000414	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000733	PMID:32109419	PCS		2/13			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000219	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000218	PMID:26721934;PMID:32109419	PCS		3/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0002236	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001347	PMID:26721934	PCS		2/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000396	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0002015	PMID:26721934	PCS		2/3			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000750	PMID:26721934;PMID:32109419	PCS		14/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0002650	PMID:32109419	PCS		4/15			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000431	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0031936	PMID:32109419	PCS		5/11			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0005280	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0002808	PMID:26721934	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0010780	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000629	PMID:26721934	PCS		2/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000508	PMID:32109419	PCS		1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000348	PMID:26721934	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0100716	PMID:26721934	PCS		1/4			P	HPO:probinson[2022-03-28]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000664	PMID:32109419	PCS		4/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0001631	PMID:32109419	PCS	HP:0003577	1/14			P	HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0007018	PMID:26721934;PMID:32109419	PCS		11/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:617061	Intellectual developmental disorder, autosomal dominant 44, with microcephaly		HP:0000347	PMID:26721934;PMID:32109419	PCS		5/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-28];HPO:probinson[2022-04-02]
OMIM:620815	MHC class II deficiency 2		HP:0002783	PMID:11313409	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0030991	PMID:37584719	PCS		1/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0001263	PMID:37584719	PCS		2/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0001890	PMID:37584719	PCS		3/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0001252	PMID:37584719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0002240	PMID:37584719	PCS		2/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0003593	PMID:37584719;PMID:11313409	PCS		13/17			C	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0002061	PMID:37584719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0012444	PMID:37584719	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0031402	PMID:11313409	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0001508	PMID:37584719	PCS		13/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0032230	PMID:37584719	PCS		2/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0011463	PMID:37584719	PCS		3/16			C	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0033431	PMID:37584719	PCS		4/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0002728	PMID:11313409	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0011462	PMID:37584719	PCS		1/16			C	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0100806	PMID:37584719	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0000007	PMID:11313409	PCS					I	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0006532	PMID:37584719	PCS		13/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0002788	PMID:37584719	PCS		7/16			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0002028	PMID:37584719;PMID:11313409	PCS		13/17			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620815	MHC class II deficiency 2		HP:0004315	PMID:11313409	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:613398	Warsaw breakage syndrome		HP:0000341	PMID:20137776	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0001034	PMID:20137776	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0000286	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-11-21]
OMIM:613398	Warsaw breakage syndrome		HP:0000340	PMID:20137776	PCS		1/1			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0003577	PMID:20137776	PCS		1/1			C	HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0000365	OMIM:613398	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613398	Warsaw breakage syndrome		HP:0001252	OMIM:613398	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613398	Warsaw breakage syndrome		HP:0001290	OMIM:613398	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613398	Warsaw breakage syndrome		HP:0001629	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-11-21]
OMIM:613398	Warsaw breakage syndrome		HP:0000954	OMIM:613398	TAS					P	HPO:skoehler[2013-03-08]
OMIM:613398	Warsaw breakage syndrome		HP:0008897	PMID:20137776	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0000218	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613398	Warsaw breakage syndrome		HP:0000378	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613398	Warsaw breakage syndrome		HP:0001249	OMIM:613398	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613398	Warsaw breakage syndrome		HP:0000154	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613398	Warsaw breakage syndrome		HP:0000274	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0000252	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0001263	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0004691	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-11-21]
OMIM:613398	Warsaw breakage syndrome		HP:0001636	OMIM:613398	TAS		HP:0040283			P	HPO:skoehler[2013-03-08]
OMIM:613398	Warsaw breakage syndrome		HP:0000965	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613398	Warsaw breakage syndrome		HP:0008586	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-11-21]
OMIM:613398	Warsaw breakage syndrome		HP:0000007	PMID:20137776	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0004209	PMID:20137776	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0001511	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:613398	Warsaw breakage syndrome		HP:0000588	PMID:20137776	PCS		1/1			P	HPO:skoehler[2012-11-21]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0003015	OMIM:259700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0010628	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0006824	PMID:10888887	PCS		1/5			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0031846	PMID:34210262	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000365	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001250	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0003155	OMIM:259700;PMID:34210262	PCS		11/11			P	HPO:probinson[2021-07-05];HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0002240	PMID:10888887	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0003593	PMID:10888887	PCS		5/5			C	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0005450	PMID:34210262	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001508	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000639	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0011002	PMID:34210262;PMID:10888887	PCS		11/11			P	HPO:probinson[2021-07-05];HPO:skoehler[2015-01-27];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001903	PMID:34210262;PMID:10888887	PCS		3/6			P	HPO:probinson[2021-07-05];HPO:skoehler[2012-10-17];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0011001	PMID:34210262	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000618	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000238	PMID:10888887	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0004618	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0002812	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0025435	PMID:34210262	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000256	PMID:34210262;PMID:10888887	PCS		2/6			P	HPO:probinson[2021-07-05];HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000597	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0002756	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001744	PMID:10888887	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0002754	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000670	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0007209	OMIM:259700	TAS					P	HPO:skoehler[2013-10-22]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001363	PMID:34210262	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001281	OMIM:259700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000007	PMID:10888887	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000648	PMID:10888887	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0000505	PMID:10888887	PCS		2/5			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0002901	PMID:34210262;PMID:10888887	PCS		3/6			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0002007	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001873	PMID:10888887	PCS		2/5			P	HPO:probinson[2021-07-05]
OMIM:259700	Osteopetrosis, autosomal recessive 1		HP:0001876	OMIM:259700	IEA					P	HPO:iea[2009-02-17]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001276	PMID:19559399	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0003577	PMID:19559399	PCS		5/8			C	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000463	PMID:19559399	PCS		7/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001156	PMID:19559399	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001250	PMID:19559399	PCS		3/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0010808	PMID:19559399	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000280	PMID:19559399	PCS		7/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0012444	PMID:19559399	PCS		1/8			P	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0009085	PMID:19559399	PCS		6/6			P	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001508	PMID:19559399	PCS		8/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001629	PMID:19559399	PCS		6/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0011461	PMID:19559399	PCS		3/8			C	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001305	PMID:19559399	PCS		2/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000238	PMID:19559399	PCS		4/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001800	PMID:19559399	PCS		6/6			P	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001643	PMID:19559399	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0002678	PMID:19559399	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000278	PMID:19559399	PCS		7/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000175	PMID:19559399	PCS		3/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000233	PMID:19559399	PCS		7/7			P	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000193	PMID:19559399	PCS		3/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0005484	PMID:19559399	PCS		8/8			P	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000470	PMID:19559399	PCS		7/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0011344	PMID:19559399	PCS		8/8			P	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0003819	PMID:19559399	PCS					C	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001639	PMID:19559399	PCS		4/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000407	PMID:19559399	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000965	PMID:19559399	PCS		7/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001339	PMID:19559399	PCS		3/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001537	PMID:19559399	PCS		4/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000007	PMID:19559399	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001511	PMID:19559399	PCS		3/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0000028	PMID:19559399	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0001612	PMID:19559399	PCS		4/6			P	HPO:probinson[2022-06-11]
OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		HP:0006129	PMID:19559399	PCS		6/6			P	HPO:probinson[2022-06-11]
OMIM:614391	Pregnancy loss, recurrent, susceptibility to, 3		HP:0011462	PMID:17339269	PCS					C	HPO:probinson[2023-02-23]
OMIM:614391	Pregnancy loss, recurrent, susceptibility to, 3		HP:0200067	PMID:17339269	PCS					H	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-23]
OMIM:614391	Pregnancy loss, recurrent, susceptibility to, 3		HP:0000006	PMID:17339269	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-23]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0003676	OMIM:616586	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0004322	OMIM:616586	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0002120	PMID:26026163	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0000020	PMID:26026163	PCS		4/6			P	HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0003593	PMID:26026163	PCS		4/6			C	HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0000518	PMID:26026163	PCS		1/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0009027	OMIM:616586	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0007024	PMID:26026163	PCS		2/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001249	PMID:26026163	PCS		6/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001347	PMID:26026163	PCS		5/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0000016	PMID:26026163	PCS		1/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0003202	PMID:26026163	PCS		4/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0000252	PMID:26026163	PCS		4/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0003621	PMID:26026163	PCS		2/6			C	HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001344	PMID:26026163	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0003487	PMID:26026163	PCS		5/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001288	PMID:26026163	PCS		6/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001260	OMIM:616586	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001263	PMID:26026163	PCS		6/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0007371	PMID:26026163	PCS		1/6			P	HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001999	OMIM:616586	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0000007	PMID:26026163	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001258	PMID:26026163	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001510	OMIM:616586	TAS					P	HPO:skoehler[2015-11-15]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001257	PMID:26026163	PCS		6/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0006886	PMID:26026163	PCS		2/3			P	HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0002445	PMID:26026163	PCS		3/6			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-13]
OMIM:616586	Spastic paraplegia 9B, autosomal recessive		HP:0001337	OMIM:616586	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001276	PMID:27573165	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0002521	PMID:32369862;PMID:27573165	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0002169	PMID:27573165	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000486	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001250	PMID:27573165	PCS		4/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000020	OMIM:617698	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001252	PMID:27573165	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0003593	PMID:32369862;PMID:27573165	PCS		5/5			C	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001290	PMID:32369862;PMID:27573165	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001508	PMID:27573165	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000718	PMID:27573165	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000218	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0006610	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001324	OMIM:617698	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001347	PMID:27573165	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0002059	PMID:27573165	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000750	PMID:27573165	PCS		4/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001344	OMIM:617698	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0031936	PMID:27573165	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001266	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0003344	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0002151	PMID:27573165	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001263	PMID:32369862;PMID:27573165	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000470	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001284	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0002490	PMID:27573165	PCS		1/1			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0032988	PMID:27573165	PCS		1/4			P	HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0011097	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000007	PMID:27573165	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000648	PMID:27573165	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0000527	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0002007	PMID:32369862	PCS		1/1			P	HPO:probinson[2022-03-20]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0001257	OMIM:617698	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0002500	OMIM:617698	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617698	3-methylglutaconic aciduria, type IX		HP:0003535	PMID:32369862;PMID:27573165	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-20];HPO:probinson[2022-03-20]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000286	PMID:28742244;PMID:7593598;PMID:8253776	PCS		3/3			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0003477	PMID:7593598	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0003577	PMID:28742244	PCS		1/1			C	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000365	PMID:22246954;PMID:8253776	PCS		2/2			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000486	PMID:8253776	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000540	PMID:7593598	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0004322	PMID:28742244;PMID:7593598	PCS		2/2			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000083	OMIM:300661	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001252	PMID:22246954;PMID:7593598;PMID:8253776	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-21];HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0003196	PMID:28742244	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001251	OMIM:300661	IEA					P	HPO:iea[2009-02-17]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001270	OMIM:300661	IEA					P	HPO:iea[2009-02-17]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0008070	PMID:8253776	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0002719	PMID:22246954	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0011220	PMID:28742244;PMID:7593598	PCS		2/2			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000218	PMID:8253776	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0003149	OMIM:300661	IEA					P	HPO:iea[2009-02-17]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001249	OMIM:300661	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000154	PMID:7593598	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000494	PMID:28742244	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000791	OMIM:300661	IEA					P	HPO:iea[2009-02-17]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001263	PMID:22246954;PMID:7593598	PCS		2/2			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0003240	PMID:28742244;PMID:8253776	PCS		7/7			P	HPO:probinson[2019-01-21];HPO:probinson[2022-05-21];HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0034368	PMID:28742244	PCS	HP:0003577	1/1			P	HPO:probinson[2022-09-05]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0005280	PMID:28742244	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0003819	PMID:22246954	IEA		1/1			C	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000407	OMIM:300661	IEA					P	HPO:iea[2009-02-17]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001518	PMID:28742244	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001419	PMID:8253776	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000508	PMID:8253776	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0009830	PMID:22246954	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000601	PMID:7593598	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000444	PMID:7593598	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000047	PMID:28742244	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000028	PMID:28742244	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000501	PMID:22246954	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001997	PMID:8253776	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-01-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000369	PMID:28742244;PMID:8253776	PCS		2/2			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000545	PMID:22246954	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000325	PMID:7593598	PCS		1/1			P	HPO:probinson[2022-05-21]
OMIM:300661	Phosphoribosylpyrophosphate synthetase superactivity		HP:0002149	PMID:22246954;PMID:28742244;PMID:7593598;PMID:8253776	PCS		9/9			P	HPO:probinson[2019-01-21];HPO:probinson[2022-05-21];HPO:probinson[2022-05-21]
OMIM:616592	Kosaki overgrowth syndrome		HP:0002344	OMIM:616592	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616592	Kosaki overgrowth syndrome		HP:0001030	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000716	OMIM:616592	TAS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0011220	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000739	PMID:25454926	PCS		1/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0001548	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000219	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000974	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0001249	PMID:25454926	PCS		1/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000336	OMIM:616592	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000494	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0003621	PMID:25454926	PCS		2/2			C	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000098	PMID:25454926	PCS		1/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0002650	PMID:25454926	PCS		2/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000431	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0005280	PMID:25454926	PCS		1/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000508	PMID:25454926	PCS		1/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0001833	OMIM:616592	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616592	Kosaki overgrowth syndrome		HP:0008765	PMID:25454926	PCS		1/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000307	PMID:25454926	PCS		1/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0002944	OMIM:616592	TAS					P	HPO:skoehler[2015-10-16]
OMIM:616592	Kosaki overgrowth syndrome		HP:0020135	PMID:25454926	PCS		1/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000520	PMID:25454926	PCS		2/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0001114	PMID:25454926	PCS		1/2			P	HPO:probinson[2023-02-19];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000006	PMID:25454926	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-19]
OMIM:616592	Kosaki overgrowth syndrome		HP:0000963	PMID:25454926	PCS		1/2			P	HPO:skoehler[2015-10-16];HPO:probinson[2023-02-19]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000582	OMIM:617854	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000343	OMIM:617854	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002540	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002188	PMID:29100083	PCS		2/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002067	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001332	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001250	PMID:29100083	PCS		5/23			P	HPO:probinson[2022-10-08];HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002385	PMID:29100083	PCS		1/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001252	PMID:29100083	PCS		7/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002020	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001251	PMID:29100083	PCS		3/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0003593	PMID:29100083	PCS					C	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002061	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0012448	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0033725	PMID:29100083	PCS		2/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0031843	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000338	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000219	OMIM:617854	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000736	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0007301	PMID:29100083	PCS		2/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000218	OMIM:617854	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000411	OMIM:617854	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001249	PMID:29100083	PCS		11/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0006879	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0006956	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002312	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002136	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0002375	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001344	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000194	OMIM:617854	IEA					P	HPO:skoehler[2019-02-15]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0011968	PMID:29100083	PCS		2/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001263	PMID:29100083	PCS		9/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0005484	PMID:29100083	PCS		2/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0100710	PMID:29100083	PCS		1/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0012760	PMID:29100083	PCS		2/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000407	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000508	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000505	PMID:29100083	PCS		1/12			P	HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001257	PMID:29100083	PCS		1/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0007018	PMID:29100083	PCS		2/12			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0000006	PMID:29100083	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:617854	Intellectual developmental disorder, autosomal dominant 56		HP:0001336	PMID:29100083	PCS		2/12			P	HPO:probinson[2022-10-08];HPO:probinson[2022-10-08]
OMIM:619879	Meckel syndrome 14		HP:0003577	PMID:27894351	IEA		4/4			C	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0002089	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001750	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000463	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000062	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001395	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0002085	PMID:27894351;PMID:31411728;PMID:30851085	PCS		6/6			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0005474	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0003270	PMID:30851085	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000316	PMID:27894351;PMID:31411728	PCS		3/5			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000113	PMID:27894351;PMID:31411728;PMID:30851085	PCS		6/6			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000278	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001562	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001883	PMID:27894351	PCS		2/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001162	PMID:30851085	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001360	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000151	PMID:27894351	PCS		2/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000470	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0005180	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0100259	PMID:27894351	PCS		3/4			P	HPO:probinson[2022-06-25];HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0034199	PMID:30851085	PCS		1/1			C	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000308	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0010880	PMID:30851085	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0034198	PMID:31411728	PCS		1/1			C	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000007	PMID:27894351	PCS					I	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000568	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0006487	PMID:31411728	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0006543	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001538	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000961	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001159	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001830	PMID:30851085	PCS		1/1			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0001653	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0002107	PMID:27894351	PCS		1/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000347	PMID:27894351	PCS		2/4			P	HPO:probinson[2022-06-25]
OMIM:619879	Meckel syndrome 14		HP:0000369	PMID:27894351	PCS		3/4			P	HPO:probinson[2022-06-25]
OMIM:314600	Wildervanck syndrome		HP:0000384	OMIM:314600	IEA					P	HPO:iea[2009-02-17]
OMIM:314600	Wildervanck syndrome		HP:0000365	OMIM:314600	IEA					P	HPO:iea[2009-02-17]
OMIM:314600	Wildervanck syndrome		HP:0002949	OMIM:314600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:314600	Wildervanck syndrome		HP:0000538	OMIM:314600	IEA					P	HPO:iea[2009-02-17]
OMIM:314600	Wildervanck syndrome		HP:0000356	OMIM:314600	TAS					P	HPO:skoehler[2015-10-05]
OMIM:314600	Wildervanck syndrome		HP:0003745	OMIM:314600	TAS					I	HPO:skoehler[2015-12-30]
OMIM:314600	Wildervanck syndrome		HP:0000465	OMIM:314600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:314600	Wildervanck syndrome		HP:0006897	OMIM:314600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:314600	Wildervanck syndrome		HP:0000324	OMIM:314600	IEA					P	HPO:iea[2009-02-17]
OMIM:614385	Colorectal cancer, hereditary nonpolyposis, type 7		HP:0006716	OMIM:614385	TAS					P	HPO:probinson[2013-08-10]
OMIM:614385	Colorectal cancer, hereditary nonpolyposis, type 7		HP:0000006	OMIM:614385	TAS					I	HPO:probinson[2013-08-10]
OMIM:123000	Craniometaphyseal dysplasia		HP:0031428	PMID:20358596	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0005017	PMID:22150416	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000365	PMID:20358596;PMID:22150416;PMID:20186813	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0004322	PMID:20358596	PCS		0/3			P	HPO:probinson[2015-03-22];HPO:probinson[2024-03-08]
OMIM:123000	Craniometaphyseal dysplasia		HP:0003155	PMID:20358596;PMID:22150416	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000680	PMID:20358596	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0003593	PMID:20358596;PMID:22150416	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000360	PMID:20358596	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0005450	OMIM:123000	TAS					P	HPO:probinson[2015-03-22]
OMIM:123000	Craniometaphyseal dysplasia		HP:0003072	PMID:22150416	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000639	PMID:22150416	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0011463	PMID:20358596;PMID:22150416	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-08-05];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0011386	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000316	PMID:20358596;PMID:22150416	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-08-05];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000678	PMID:20358596	PCS		2/3			P	HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000238	PMID:22150416	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0004437	PMID:20358596;PMID:22150416	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-08-05];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000358	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000692	OMIM:123000	TAS					P	HPO:probinson[2015-03-22]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000452	PMID:20358596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0011968	PMID:20358596	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000925	PMID:20358596	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0006384	OMIM:123000	IEA					P	HPO:iea[2009-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0025405	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000689	PMID:20358596	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000648	PMID:20358596;PMID:22150416	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0004407	PMID:20358596;PMID:22150416	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-08-05];HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000006	PMID:11326272	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0002148	PMID:22150416	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000369	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0003015	PMID:20358596;PMID:22150416	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-08-05];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0003577	PMID:20358596	PCS		1/3			C	HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0010628	PMID:20358596;PMID:22150416	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-08-05];HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0003016	OMIM:123000	TAS					P	HPO:probinson[2009-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0002684	PMID:20358596;PMID:22150416;PMID:20186813	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0009085	PMID:20358596;PMID:22150416	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0012370	PMID:20186813	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0005906	PMID:20358596	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000337	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0001742	OMIM:123000	IEA					P	HPO:iea[2009-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000696	PMID:20186813	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000212	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000256	PMID:20358596;PMID:22150416	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-08-05];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000410	PMID:20358596	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0002753	PMID:20358596	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0004975	OMIM:123000	IEA					P	HPO:iea[2009-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000577	PMID:22150416	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:6001071	PMID:16980979	PCS					P	HPO:probinson[2024-08-03]
OMIM:123000	Craniometaphyseal dysplasia		HP:0002677	PMID:22150416	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0005645	PMID:22150416	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0003621	PMID:20186813	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0002694	PMID:20358596;PMID:22150416;PMID:20186813	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-08-05];HPO:probinson[2009-02-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000431	PMID:20186813	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000276	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0011225	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000506	PMID:22150416	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000426	PMID:20186813	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000867	PMID:22150416	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0002007	PMID:22150416	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:123000	Craniometaphyseal dysplasia		HP:0000303	PMID:20358596	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:123000	Craniometaphyseal dysplasia		HP:0002644	PMID:20358596	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:615925	Growth hormone deficiency, isolated partial		HP:0004322	OMIM:615925	TAS					P	HPO:probinson[2015-05-08]
OMIM:615925	Growth hormone deficiency, isolated partial		HP:0002750	OMIM:615925	TAS		HP:0040283			P	HPO:probinson[2015-05-08]
OMIM:615925	Growth hormone deficiency, isolated partial		HP:0000007	OMIM:615925	TAS					I	HPO:probinson[2015-05-08]
OMIM:615925	Growth hormone deficiency, isolated partial		HP:0008897	OMIM:615925	TAS					P	HPO:probinson[2015-05-08]
OMIM:615925	Growth hormone deficiency, isolated partial		HP:0000824	OMIM:615925	IEA					P	HPO:skoehler[2015-12-30]
OMIM:615925	Growth hormone deficiency, isolated partial		HP:0012506	OMIM:615925	TAS		HP:0040283			P	HPO:probinson[2015-05-08]
OMIM:615925	Growth hormone deficiency, isolated partial		HP:0000006	OMIM:615925	TAS					I	HPO:probinson[2015-05-08]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0010804	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000365	PMID:38054405	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0002783	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0004443	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001250	PMID:37459438;PMID:38054405	PCS		3/12			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001252	PMID:37459438	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001251	PMID:38054405	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0012389	PMID:37459438;PMID:38054405	PCS		6/15			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0033725	PMID:38054405	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000718	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0002812	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000752	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000278	PMID:38054405	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000358	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0003623	PMID:37459438	PCS		3/5			C	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000252	PMID:37459438;PMID:38054405	PCS		6/15			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001344	PMID:38054405	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0002079	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001263	PMID:37459438;PMID:38054405	PCS		15/16			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0002072	PMID:38054405	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001182	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0100023	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0100699	PMID:38054405	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0007074	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0034353	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000601	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000527	PMID:38054405	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000400	PMID:37459438;PMID:38054405	PCS		2/16			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0002788	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000369	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000006	PMID:37459438	PCS					I	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000384	PMID:38054405	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0003577	PMID:37459438	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000343	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000463	PMID:38054405	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0002282	PMID:38054405	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0034677	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001508	PMID:37459438;PMID:38054405	PCS		4/10			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000739	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000411	PMID:38054405	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001347	PMID:37459438	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0008936	PMID:37459438;PMID:38054405	PCS		13/15			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000431	PMID:38054405	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000276	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0002376	PMID:38054405	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0005487	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0003186	PMID:37459438	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0025190	PMID:37459438	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:6000989	PMID:38054405	PCS		3/5			P	HPO:probinson[2024-08-03]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0001518	PMID:38054405	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000505	PMID:38054405	PCS		0/10			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0200012	PMID:38054405	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000664	PMID:38054405	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:620746	Neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		HP:0000303	PMID:38054405	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-07-13]
OMIM:600496	Maturity-onset diabetes of the young, type III		HP:0003593	OMIM:600496	IEA					C	HPO:iea[2009-02-17]
OMIM:600496	Maturity-onset diabetes of the young, type III		HP:0003074	OMIM:600496	IEA					P	HPO:iea[2009-02-17]
OMIM:600496	Maturity-onset diabetes of the young, type III		HP:0004904	OMIM:600496	IEA					P	HPO:iea[2009-02-17]
OMIM:600496	Maturity-onset diabetes of the young, type III		HP:0005978	OMIM:600496	IEA					P	HPO:iea[2009-02-17]
OMIM:600496	Maturity-onset diabetes of the young, type III		HP:0000006	OMIM:600496	IEA					I	HPO:iea[2009-02-17]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0011807	OMIM:310300	TAS					P	HPO:probinson[2013-12-15]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0003202	PMID:29250285	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0001771	PMID:29250285	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0003621	PMID:29250285;OMIM:310300	PCS		11/11			C	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0003236	PMID:29250285	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0004631	OMIM:310300	IEA					P	HPO:iea[2009-02-17]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0000464	OMIM:310300	IEA					P	HPO:iea[2009-02-17]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0003198	OMIM:310300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0011705	PMID:29250285	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0001692	OMIM:310300	IEA					P	HPO:iea[2009-02-17]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0006380	PMID:29250285	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0001419	OMIM:310300	IEA					I	HPO:iea[2009-02-17]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0011463	OMIM:310300	TAS					C	HPO:probinson[2013-12-15]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0033122	PMID:29250285	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0000767	OMIM:310300	TAS				HP:0012825	P	HPO:probinson[2013-12-15]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0002515	OMIM:310300	IEA					P	HPO:iea[2009-02-17]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0002505	PMID:29250285	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0001962	PMID:29250285	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0002987	PMID:29250285	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0001645	OMIM:310300	TAS					P	HPO:probinson[2013-12-15]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0003677	PMID:29250285	PCS					C	HPO:probinson[2009-02-17];HPO:probinson[2022-07-11]
OMIM:310300	Emery-Dreifuss muscular dystrophy 1, X-linked		HP:0001678	OMIM:310300	IEA					P	HPO:iea[2009-02-17]
OMIM:127500	Dyschromatosis universalis hereditaria		HP:0003593	OMIM:127500	TAS					C	HPO:skoehler[2009-02-17]
OMIM:127500	Dyschromatosis universalis hereditaria		HP:0007441	OMIM:127500	IEA					P	HPO:iea[2009-02-17]
OMIM:127500	Dyschromatosis universalis hereditaria		HP:0000006	OMIM:127500	IEA					I	HPO:iea[2009-02-17]
OMIM:203340	Microcephaly - albinism - digital anomalies		HP:0001022	OMIM:203340	IEA					P	HPO:skoehler[2015-01-27]
OMIM:619689	Spermatogenic failure 63		HP:0034011	PMID:32111475	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619689	Spermatogenic failure 63		HP:0011462	PMID:32111475	PCS		2/2			C	HPO:probinson[2022-03-21]
OMIM:619689	Spermatogenic failure 63		HP:0003251	PMID:32111475	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619689	Spermatogenic failure 63		HP:0000007	PMID:32111475	PCS					I	HPO:probinson[2022-03-21]
OMIM:619689	Spermatogenic failure 63		HP:0008734	PMID:32111475	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619689	Spermatogenic failure 63		HP:0000798	PMID:32111475	PCS		2/2			P	HPO:probinson[2022-03-21]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0003477	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0003510	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0025352	PMID:34403372	PCS					I	HPO:probinson[2022-06-12];HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0002059	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0000252	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0003431	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0002376	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0001250	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0001371	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0001263	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0001284	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0012704	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0010976	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0033725	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0000518	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0000821	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0001308	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0002119	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12];HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0002415	PMID:34403372	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:619851	Leukodystrophy, hypomyelinating, 24		HP:0003623	PMID:34403372	PCS		1/1			C	HPO:probinson[2022-06-12]
OMIM:106280	Ankyloglossia with or without tooth anomalies		HP:0010296	OMIM:106280	IEA					P	HPO:skoehler[2010-06-18]
OMIM:106280	Ankyloglossia with or without tooth anomalies		HP:0011069	OMIM:106280	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:106280	Ankyloglossia with or without tooth anomalies		HP:0000006	OMIM:106280	IEA					I	HPO:iea[2009-02-17]
OMIM:134540	Factor IX and factor XI, combined deficiency of		HP:0001929	OMIM:134540	IEA					P	HPO:probinson[2015-02-15]
OMIM:134540	Factor IX and factor XI, combined deficiency of		HP:0011858	OMIM:134540	IEA					P	HPO:probinson[2015-02-15]
OMIM:134540	Factor IX and factor XI, combined deficiency of		HP:0000006	OMIM:134540	IEA					I	HPO:probinson[2015-02-15]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0007759	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0000100	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0004322	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0002086	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0000093	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0001518	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0006462	OMIM:215250	TAS					P	HPO:probinson[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0008155	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0000007	OMIM:215250	IEA					I	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0001648	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0006577	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0002843	OMIM:215250	IEA					P	HPO:skoehler[2015-01-19]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0002720	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:215250	Chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome		HP:0002721	OMIM:215250	IEA					P	HPO:iea[2009-02-17]
OMIM:619845	Retinitis pigmentosa 93		HP:0000550	PMID:30267408	PCS		3/3			P	HPO:probinson[2022-06-06]
OMIM:619845	Retinitis pigmentosa 93		HP:0001133	PMID:30267408	PCS		3/3			P	HPO:probinson[2022-06-06]
OMIM:619845	Retinitis pigmentosa 93		HP:0003577	PMID:30267408	PCS		1/3			C	HPO:probinson[2022-06-06]
OMIM:619845	Retinitis pigmentosa 93		HP:0011462	PMID:30267408	PCS		2/3			C	HPO:probinson[2022-06-06]
OMIM:619845	Retinitis pigmentosa 93		HP:0000007	PMID:30267408	PCS					I	HPO:probinson[2022-06-06]
OMIM:619845	Retinitis pigmentosa 93		HP:0007663	PMID:30267408	PCS		3/3			P	HPO:probinson[2022-06-06]
OMIM:619845	Retinitis pigmentosa 93		HP:0032027	PMID:30267408	PCS		1/3			P	HPO:probinson[2022-06-06]
OMIM:619845	Retinitis pigmentosa 93		HP:0000510	PMID:30267408	PCS		3/3			P	HPO:probinson[2022-06-06];HPO:probinson[2022-06-06]
OMIM:194090	Wilms tumor 3		HP:0002667	OMIM:194090	IEA					P	HPO:iea[2009-02-17]
OMIM:194090	Wilms tumor 3		HP:0000006	OMIM:194090	IEA					I	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000286	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000582	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001770	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0002983	OMIM:211750	TAS					P	HPO:skoehler[2012-10-17]
OMIM:211750	C syndrome		HP:0000486	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000243	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000463	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0004322	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001250	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001252	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0003196	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0002240	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0010049	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001290	OMIM:211750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:211750	C syndrome		HP:0001508	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001629	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0009100	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0009465	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0009466	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000218	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0030084	OMIM:211750	TAS					P	HPO:skoehler[2014-09-21]
OMIM:211750	C syndrome		HP:0001643	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000358	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000973	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000154	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000252	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0009826	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000431	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0002650	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0002750	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001162	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001263	OMIM:211750	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000191	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0003083	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000803	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0002827	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001539	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0008665	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0001830	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0006643	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000028	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000347	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000369	OMIM:211750	IEA					P	HPO:iea[2009-02-17]
OMIM:211750	C syndrome		HP:0000006	OMIM:211750	IEA					I	HPO:skoehler[2019-04-18]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0003323	PMID:24911150	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0002015	PMID:24911150	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0000252	PMID:24911150	PCS		3/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0003676	PMID:24911150	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0000992	PMID:24911150	PCS		4/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0001761	PMID:24911150	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0004322	PMID:24911150	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0001272	PMID:24911150	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0001260	PMID:24911150	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0001263	PMID:24911150	PCS		4/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0001251	PMID:24911150	PCS		4/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0003593	PMID:24911150	PCS		4/4			C	HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0034697	PMID:24911150	PCS		4/4			P	HPO:probinson[2023-06-05]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0002180	PMID:24911150	PCS		4/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0034392	PMID:24911150	PCS		1/4			P	HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0000407	PMID:24911150	PCS		4/4			P	HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0031087	PMID:24911150	PCS		2/4			P	HPO:probinson[2023-04-15];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0000613	PMID:24911150	PCS		4/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0000007	PMID:24911150	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0000524	PMID:24911150	PCS		3/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0002317	PMID:24911150	PCS		4/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0001324	PMID:24911150	PCS				HP:0003676	P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0000776	PMID:24911150	PCS		1/4			P	HPO:probinson[2023-04-15]
OMIM:615919	Ataxia-telangiectasia-like disorder 2		HP:0005328	PMID:24911150	PCS		1/2			P	HPO:probinson[2023-04-15]
OMIM:269600	Sea-Blue histiocyte disease		HP:0031956	PMID:11095479	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:269600	Sea-Blue histiocyte disease		HP:0002221	OMIM:269600	IEA					P	HPO:iea[2009-02-17]
OMIM:269600	Sea-Blue histiocyte disease		HP:0001982	PMID:11095479	PCS		2/2			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-05-28]
OMIM:269600	Sea-Blue histiocyte disease		HP:0003651	PMID:11095479	IEA		2/2			P	HPO:probinson[2022-05-28]
OMIM:269600	Sea-Blue histiocyte disease		HP:0003581	PMID:11095479	PCS		2/2			C	HPO:probinson[2022-05-28]
OMIM:269600	Sea-Blue histiocyte disease		HP:0001394	OMIM:269600	IEA					P	HPO:iea[2009-02-17]
OMIM:269600	Sea-Blue histiocyte disease		HP:0000007	PMID:11095479	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:269600	Sea-Blue histiocyte disease		HP:0001873	PMID:11095479	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:269600	Sea-Blue histiocyte disease		HP:0001744	PMID:11095479	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:269600	Sea-Blue histiocyte disease		HP:0031964	PMID:11095479	PCS		1/1			P	HPO:probinson[2022-05-28]
OMIM:614434	Cutis laxa, autosomal dominant 2		HP:0100678	OMIM:614434	TAS					P	HPO:probinson[2013-08-10]
OMIM:614434	Cutis laxa, autosomal dominant 2		HP:0002650	OMIM:614434	TAS					P	HPO:probinson[2013-08-10]
OMIM:614434	Cutis laxa, autosomal dominant 2		HP:0001653	OMIM:614434	TAS					P	HPO:probinson[2013-08-10]
OMIM:614434	Cutis laxa, autosomal dominant 2		HP:0000006	OMIM:614434	TAS					I	HPO:probinson[2013-08-10]
OMIM:614434	Cutis laxa, autosomal dominant 2		HP:0000973	OMIM:614434	TAS					P	HPO:probinson[2013-08-10]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0004325	PMID:32707087	PCS		3/14			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0003577	PMID:32707087	PCS		10/10			C	HPO:probinson[2022-06-27]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0004322	PMID:32707087	PCS		5/10			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0100490	PMID:32707087	PCS		14/15			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000160	PMID:32707087	PCS		10/15			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000581	PMID:32707087	PCS		1/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0003273	PMID:32707087	PCS		6/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0410030	PMID:32707087	PCS		2/14			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0006070	PMID:32707087	PCS		2/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000218	PMID:32707087	PCS		2/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000278	PMID:32707087	PCS		2/15			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000175	PMID:32707087	PCS		2/14			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0002650	PMID:32707087	PCS		6/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0001762	PMID:32707087	PCS		9/16			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000233	PMID:32707087	PCS		2/8			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0003044	PMID:32707087	PCS		2/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000193	PMID:32707087	PCS		1/8			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000470	PMID:32707087	PCS		2/10			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0001181	PMID:32707087	PCS		2/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0033357	PMID:32707087	PCS		4/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0006380	PMID:32707087	PCS		6/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0001838	PMID:32707087	PCS		5/10			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0010880	PMID:32707087	PCS		1/10			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000007	PMID:32707087	PCS					I	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000205	PMID:32707087	PCS		2/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0001239	PMID:32707087	PCS		11/15			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0001836	PMID:32707087	PCS		2/13			P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0004209	PMID:32707087	PCS		1/15			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000466	PMID:32707087	PCS		4/9			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0002987	PMID:32707087	PCS		4/12			P	HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000006	PMID:32707087	PCS					I	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:619110	Arthrogryposis, distal, type 1C		HP:0000028	PMID:32707087	PCS		3/5	MALE		P	HPO:probinson[2021-03-08];HPO:probinson[2021-03-08]
OMIM:224700	Ebstein anomaly		HP:0025478	OMIM:224700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:224700	Ebstein anomaly		HP:0005110	OMIM:224700	IEA					P	HPO:iea[2009-02-17]
OMIM:224700	Ebstein anomaly		HP:0000007	OMIM:224700	IEA					I	HPO:iea[2009-02-17]
OMIM:224700	Ebstein anomaly		HP:0011712	OMIM:224700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224700	Ebstein anomaly		HP:0004309	OMIM:224700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:224700	Ebstein anomaly		HP:0001631	OMIM:224700	IEA					P	HPO:iea[2009-02-17]
OMIM:224700	Ebstein anomaly		HP:0010316	OMIM:224700	IEA					P	HPO:iea[2009-02-17]
OMIM:224700	Ebstein anomaly		HP:0001645	OMIM:224700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000286	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0001572	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000582	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000189	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000463	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0004322	PMID:23269703	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000581	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0001251	PMID:23269703	PCS		0/1			P	HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000280	PMID:23269703	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0008070	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0001508	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0001903	OMIM:617883	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617883	Fanconi anemia, complementation group S		HP:0011463	PMID:23269703	PCS		1/1			C	HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0040012	OMIM:617883	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000316	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0009623	OMIM:617883	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0030084	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0001249	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000215	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0025318	PMID:23269703	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000252	PMID:23269703	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0003002	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000750	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000430	PMID:23269703	PCS		1/1			P	HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0001263	PMID:23269703	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000294	PMID:23269703	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0100615	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000426	PMID:23269703	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000007	PMID:23269703	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-28]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000689	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000568	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617883	Fanconi anemia, complementation group S		HP:0000527	OMIM:617883	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609465	Al-Gazali syndrome		HP:0007957	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0001561	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0030884	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0005037	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0011800	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0001508	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0000938	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0000007	PMID:25149931	PCS					I	HPO:probinson[2021-10-21];HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0001239	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0002757	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0006532	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0000647	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0009836	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0000347	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0003865	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0001776	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:609465	Al-Gazali syndrome		HP:0000126	PMID:25149931	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:220200	Dandy-Walker syndrome		HP:0006824	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0002078	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0000639	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0002198	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0000238	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0000931	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0000933	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0003745	OMIM:220200	TAS					I	HPO:skoehler[2017-07-13]
OMIM:220200	Dandy-Walker syndrome		HP:0000930	OMIM:220200	IEA					P	HPO:iea[2009-02-17]
OMIM:220200	Dandy-Walker syndrome		HP:0002951	OMIM:220200	TAS					P	HPO:probinson[2012-06-10]
OMIM:220200	Dandy-Walker syndrome		HP:0002335	OMIM:220200	TAS					P	HPO:probinson[2012-06-10]
OMIM:113100	Brachydactyly, type C		HP:0001772	OMIM:113100	IEA		HP:0040283			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0004322	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0001156	PMID:28391997	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0004220	PMID:28391997	PCS		2/3			P	HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0009461	OMIM:113100	IEA		HP:0040281			P	HPO:probinson[2012-06-09]
OMIM:113100	Brachydactyly, type C		HP:0009463	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0010034	PMID:28391997	PCS		1/3			P	HPO:iea[2009-10-01];HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0009464	PMID:28391997	PCS		2/3			P	HPO:iea[2009-10-01];HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0009324	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009587	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009523	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009349	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009527	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0011929	OMIM:113100	TAS					P	HPO:probinson[2012-06-10]
OMIM:113100	Brachydactyly, type C		HP:0001762	OMIM:113100	IEA		HP:0040283			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0002750	PMID:28391997	PCS		1/2			P	HPO:iea[2009-10-01];HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0001162	PMID:28391997	PCS	HP:0003577	1/3			P	HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0003067	OMIM:113100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:113100	Brachydactyly, type C		HP:0010259	OMIM:113100	IEA		HP:0040281			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009331	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009495	OMIM:113100	IEA		HP:0040281			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009575	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0032078	PMID:28391997	PCS		1/3			P	HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0009456	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009577	PMID:28391997	IEA		2/3			P	HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0009356	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009436	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009534	PMID:28391997	PCS		2/3			P	HPO:iea[2009-10-01];HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0004209	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009536	OMIM:113100	IEA		HP:0040281			P	HPO:probinson[2012-06-09]
OMIM:113100	Brachydactyly, type C		HP:0000006	PMID:9288091	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:113100	Brachydactyly, type C		HP:0009417	OMIM:113100	IEA		HP:0040281			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0006206	OMIM:113100	TAS					P	HPO:probinson[2012-06-10]
OMIM:113100	Brachydactyly, type C		HP:0009516	OMIM:113100	IEA		HP:0040282			P	HPO:iea[2009-10-01]
OMIM:113100	Brachydactyly, type C		HP:0009439	PMID:28391997	PCS		2/3			P	HPO:probinson[2022-05-15]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0000662	PMID:23246293	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0000486	PMID:23246293	PCS		1/2			P	HPO:skoehler[2013-03-08];HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0011463	PMID:23246293	PCS		2/2			C	HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0011958	PMID:23246293	PCS		1/2			P	HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0000007	PMID:23246293	PCS					I	HPO:skoehler[2013-03-08];HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0007663	PMID:23246293	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0007642	PMID:23246293	PCS		2/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0007984	PMID:23246293	PCS		1/2			P	HPO:probinson[2023-02-12]
OMIM:615058	Night blindness, congenital stationary, type 1F		HP:0011003	PMID:23246293	PCS		2/2			P	HPO:probinson[2023-02-12]
OMIM:614346	Intellectual developmental disorder, autosomal recessive 25		HP:0000750	OMIM:614346	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614346	Intellectual developmental disorder, autosomal recessive 25		HP:0000739	OMIM:614346	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614346	Intellectual developmental disorder, autosomal recessive 25		HP:0000007	OMIM:614346	TAS					I	HPO:skoehler[2017-07-13]
OMIM:614346	Intellectual developmental disorder, autosomal recessive 25		HP:0001270	OMIM:614346	TAS					P	HPO:skoehler[2017-07-13]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0003621	PMID:30976738;PMID:34555379	PCS		2/9			C	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0001396	PMID:30976738;PMID:30250217	PCS		7/7			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0031956	PMID:30976738	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0003124	PMID:30976738	PCS		1/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0003155	PMID:30976738	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0030991	PMID:30250217	PCS		1/4			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0001395	PMID:34555379	PCS		4/5			P	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0003593	PMID:30976738;PMID:34555379	PCS		5/9			C	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0002240	PMID:30976738	PCS		2/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0001394	PMID:30976738;PMID:34555379	PCS		3/7			P	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0002040	PMID:30250217	PCS		1/4			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0030948	PMID:30976738;PMID:34555379;PMID:30250217	PCS		13/13			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0012202	PMID:30976738	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0012852	PMID:30976738	PCS		1/2			P	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0031964	PMID:30976738	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0002908	PMID:30976738	PCS		2/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0001409	PMID:30250217	PCS		1/4			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0011463	PMID:34555379	PCS		1/6			C	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0001408	PMID:34555379	PCS		4/5			P	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0006254	PMID:30976738	PCS		2/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0000007	PMID:30976738	PCS					I	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0000989	PMID:34555379	PCS		4/6			P	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0000952	PMID:30976738	PCS		3/3			P	HPO:probinson[2022-02-08]
OMIM:619662	Cholestasis, progressive familial intrahepatic, 8		HP:0003623	PMID:34555379	IEA		1/6			C	HPO:probinson[2022-02-08];HPO:probinson[2022-02-08]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002069	PMID:37951597	PCS		3/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000286	PMID:37951597	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000486	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001332	PMID:37951597	PCS		6/16			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001250	PMID:37951597	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000083	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001252	PMID:37951597	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001251	PMID:37951597	PCS		33/39			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002061	PMID:37951597	PCS		27/34			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000280	PMID:37951597	PCS		22/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0012469	PMID:37951597	PCS		1/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000639	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000718	PMID:37951597	PCS		14/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000238	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002553	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0025331	PMID:37951597	PCS		12/27			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000175	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001344	PMID:37951597	PCS		5/41			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002870	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0030302	PMID:37951597	PCS		4/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001300	PMID:37951597	PCS		11/26			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002079	PMID:37951597	PCS		5/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001382	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000490	PMID:37951597	PCS		16/33			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001263	PMID:37951597	PCS		45/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002591	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001182	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0011003	PMID:37951597	PCS		3/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000969	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000729	PMID:37951597	PCS		13/27			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001338	PMID:37951597	PCS		4/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000007	PMID:37951597	PCS					I	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0025403	PMID:37951597	PCS		29/30			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002788	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001257	PMID:37951597	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0007359	PMID:37951597	PCS		3/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000047	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000322	PMID:37951597	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001337	PMID:37951597	PCS		22/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0006986	PMID:37951597	PCS		9/22			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000445	PMID:37951597	PCS		24/36			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000582	PMID:37951597	PCS		20/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000662	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001278	PMID:37951597	PCS		0/15			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002123	PMID:37951597	PCS		2/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000540	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002684	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001272	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000020	PMID:37951597	PCS		13/23			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001274	PMID:37951597	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001394	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0012444	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0025161	PMID:37951597	PCS		19/36			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0100033	PMID:37951597	PCS		7/19			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000819	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0007068	PMID:37951597	PCS		5/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000219	PMID:37951597	PCS		23/36			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002119	PMID:37951597	PCS		3/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001320	PMID:37951597	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000750	PMID:37951597	PCS		36/36			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001762	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002650	PMID:37951597	PCS		3/27			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0031936	PMID:37951597	PCS		32/33			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000232	PMID:37951597	PCS		16/35			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000276	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0030048	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0010819	PMID:37951597	PCS		1/37			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002172	PMID:37951597	PCS		15/25			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0005280	PMID:37951597	PCS		24/36			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0002808	PMID:37951597	PCS		2/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000506	PMID:37951597	PCS		3/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000822	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0100716	PMID:37951597	PCS		8/34			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000505	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0200055	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000303	PMID:37951597	PCS		9/34			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001876	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0001513	PMID:37951597	PCS		6/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:620785	Neurodevelopmental disorder with progressive movement abnormalities		HP:0000028	PMID:37951597	PCS		1/45			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000286	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000365	PMID:16510655	PCS		8/27			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000486	PMID:28584669;PMID:16510655	PCS		12/27			P	ORCID:0000-0002-0736-9199[2024-05-22];HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001250	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000160	PMID:28584669	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0003273	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0003273	PMID:16510655	IEA	HP:0003577	15/26			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001373	PMID:16510655	PCS		3/26			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0003196	PMID:20924721	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0000041	PMID:28584669	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0003593	PMID:20924721	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0012785	PMID:16510655	PCS	HP:0003577	28/28			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0003191	PMID:28584669;PMID:20924721	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0011220	OMIM:193700	TAS					P	HPO:probinson[2012-03-18]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0000316	PMID:28584669	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0001845	PMID:20924721	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000678	PMID:16510655	PCS		14/14			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0008897	OMIM:193700	TAS					P	HPO:probinson[2012-03-18]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001324	OMIM:193700	TAS					P	HPO:skoehler[2012-11-26]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000951	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002751	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000252	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000298	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0003044	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000490	PMID:20924721	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0010751	OMIM:193700	TAS					P	HPO:skoehler[2012-11-26]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001181	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0012385	PMID:28584669;PMID:20924721	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2024-05-22];ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0006380	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0006380	PMID:16510655	PCS	HP:0003577	7/27			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002829	PMID:16510655	PCS		2/11			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002827	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000205	PMID:28584669	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002987	PMID:16510655	PCS	HP:0003577	11/25			P	HP:probinson[2019-04-08];HPO:probinson[2019-07-03]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0000047	PMID:28584669	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000006	PMID:25256237	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0000369	PMID:28584669	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001611	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002047	PMID:16510655	PCS		3/19			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0005997	PMID:16510655	PCS	HP:0003577	24/27			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0003577	PMID:28584669	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0005830	OMIM:193700	TAS					P	HPO:probinson[2012-03-18]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000343	PMID:20924721	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002365	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000023	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001272	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0003298	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000581	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0100790	PMID:16510655	PCS		6/26			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001270	PMID:16510655	PCS		28/28			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001193	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0012368	PMID:20924721	PCS		1/1			P	HPO:skoehler[2013-10-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001508	OMIM:193700	TAS					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0008872	PMID:16510655	PCS		HP:0040281			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002757	PMID:16510655	PCS		6/23			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000218	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001623	OMIM:193700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001562	PMID:16510655	PCS		2/17			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001561	PMID:16510655	PCS		5/17			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002650	PMID:16510655	PCS		22/26			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001762	PMID:28584669;PMID:20924721	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-22];HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000431	PMID:28584669	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0006958	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000430	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000272	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000470	PMID:20924721	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0011824	OMIM:193700	TAS					P	HPO:probinson[2012-04-30]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0005280	PMID:28584669;PMID:20924721	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001838	PMID:28584669	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0009473	OMIM:193700	TAS					P	HPO:probinson[2012-03-18]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001518	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000506	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000508	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001558	PMID:16510655	PCS		9/17			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0001239	PMID:16510655	PCS	HP:0003577	23/27			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0002205	PMID:16510655	PCS		9/27			P	HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000028	PMID:16510655	PCS		5/12	MALE		P	HPO:iea[2009-02-17];HP:probinson[2019-04-08]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000303	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:193700	Arthrogryposis, distal, type 2A (Freeman-Sheldon)		HP:0000347	PMID:28584669	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-22]
OMIM:193700	Arthrogryposis, distal, type 2A		HP:0000346	OMIM:193700	IEA					P	HPO:iea[2009-02-17]
OMIM:614420	Systemic lupus erythematosus 16		HP:0003621	PMID:22019780	PCS		8/17			C	HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0033726	PMID:22019780	PCS		11/17			P	HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0005421	PMID:22019780	PCS		17/17			P	HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0011463	PMID:22019780	PCS		9/17			C	HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0020151	PMID:22019780	PCS		16/17			P	HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0003493	PMID:22019780	PCS		17/17			P	HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0000007	PMID:22019780	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0002725	PMID:22019780	PCS		17/17			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0045042	PMID:22019780	PCS		17/17			P	HPO:probinson[2022-10-10]
OMIM:614420	Systemic lupus erythematosus 16		HP:0032229	PMID:22019780	PCS		11/17			P	HPO:probinson[2022-10-10]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000582	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0004467	PMID:26111080	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0003577	PMID:26111080	PCS		2/2			C	HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0002089	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000343	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0020073	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0004322	OMIM:145420	IEA					P	HPO:skoehler[2019-04-18]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000463	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0001195	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0004442	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0025269	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0003196	OMIM:145420	IEA					P	HPO:iea[2009-02-17]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0004440	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0001629	PMID:26111080	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0011220	OMIM:145420	TAS					P	HPO:skoehler[2012-10-17]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000739	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000316	PMID:26111080	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-11];HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0002616	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000678	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000219	PMID:26111080	PCS		2/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000813	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0001169	OMIM:145420	IEA					P	HPO:skoehler[2010-06-20]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0001488	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0002553	OMIM:145420	IEA					P	HPO:skoehler[2019-02-22]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000494	OMIM:145420	IEA					P	HPO:iea[2009-02-17]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000431	OMIM:145420	TAS					P	HPO:probinson[2012-04-24]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000695	PMID:26111080	PCS		3/5			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11];HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000034	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0001263	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0005280	OMIM:145420	TAS					P	HPO:probinson[2012-04-24]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000729	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000349	OMIM:145420	IEA					P	HPO:iea[2009-02-17]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0001539	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0200055	PMID:26111080;OMIM:145420	PCS		11/12			P	HPO:skoehler[2019-04-18];HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0002007	PMID:26111080	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0001631	PMID:26111080	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000347	PMID:26111080	PCS		1/2			P	HP:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000006	PMID:26111080	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:145420	Teebi hypertelorism syndrome 1		HP:0000049	PMID:26111080	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:229230	Fraser-Like syndrome		HP:0001607	OMIM:229230	TAS					P	HPO:probinson[2009-02-17]
OMIM:229230	Fraser-Like syndrome		HP:0009540	OMIM:229230	TAS					P	HPO:probinson[2012-07-16]
OMIM:229230	Fraser-Like syndrome		HP:0001845	OMIM:229230	TAS					P	HPO:probinson[2012-07-16]
OMIM:229230	Fraser-Like syndrome		HP:0000007	OMIM:229230	TAS					I	HPO:probinson[2009-02-17]
OMIM:229230	Fraser-Like syndrome		HP:0000138	OMIM:229230	TAS					P	HPO:probinson[2009-02-17]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0001298	OMIM:618232	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0001254	OMIM:618232	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0011968	OMIM:618232	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0002791	OMIM:618232	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0001250	OMIM:618232	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0006829	OMIM:618232	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0011923	PMID:15372108	PCS		1/1			P	HPO:probinson[2022-12-20]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0000639	OMIM:618232	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0000007	PMID:15372108	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-20]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0005957	OMIM:618232	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0003811	PMID:15372108	PCS		2/2			C	HPO:probinson[2022-12-20]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0003128	PMID:15372108	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-20]
OMIM:618232	Mitochondrial complex I deficiency, nuclear type 9		HP:0003623	PMID:15372108	PCS		2/2			C	HPO:probinson[2022-12-20]
OMIM:128800	Ear without helix		HP:0011039	OMIM:128800	TAS					P	HPO:probinson[2021-07-14]
OMIM:128800	Ear without helix		HP:0000006	OMIM:128800	IEA					I	HPO:iea[2009-02-17]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000286	PMID:27453576	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0003577	PMID:27453576	PCS		10/10			C	HPO:skoehler[2017-07-13]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000486	PMID:27453576	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000463	PMID:27453576	PCS		2/8			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0004322	PMID:27453576	PCS		2/9			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0005274	PMID:27453576	PCS		4/8			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000219	PMID:27453576	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000378	PMID:27453576	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000278	PMID:27453576	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0001249	PMID:27453576	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0006855	PMID:27453576	PCS		1/6			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000396	PMID:27453576	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0004611	PMID:27453576	PCS		1/9			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000494	PMID:27453576	PCS		4/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000252	PMID:27453576	PCS		5/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0002136	PMID:27453576	PCS		2/8			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0002078	PMID:27453576	PCS		1/8			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000232	PMID:27453576	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0031936	PMID:27453576	PCS		8/8			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0001382	PMID:27453576	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000592	PMID:27453576	PCS		3/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0001263	PMID:27453576	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0011904	PMID:27453576	PCS		6/6			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0011800	PMID:27453576	PCS		6/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0002070	PMID:27453576	PCS		1/8			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0100023	PMID:27453576	PCS		2/9			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000729	PMID:27453576	PCS		3/10			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0100716	PMID:27453576	PCS		1/9			P	HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000006	PMID:27453576	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000369	PMID:27453576	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617101	Intellectual developmental disorder with persistence of fetal hemoglobin		HP:0000347	PMID:27453576	PCS		1/9			P	HPO:probinson[2023-02-20]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0003774	OMIM:137920	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0030997	OMIM:137920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000089	PMID:15930087	PCS		1/23			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000122	PMID:15930087	PCS		1/23			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0002120	OMIM:137920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0003076	OMIM:137920	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:6000156	PMID:16249435	PCS		9/15			P	HPO:probinson[2024-03-08]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0012207	OMIM:137920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000819	PMID:15930087	PCS	HP:0003577	HP:0040282			P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0012210	PMID:15930087	PCS		2/23			P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0011462	PMID:16249435	PCS					C	HPO:probinson[2024-03-08]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000813	PMID:15930087	PCS		1/23			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0002910	PMID:15930087	PCS					P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000077	PMID:15930087	PCS		78/88			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0004379	PMID:15930087	PCS		4/7			P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0030424	OMIM:137920	TAS					P	HPO:skoehler[2015-08-05]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000013	PMID:15930087	PCS		1/23			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000078	PMID:15930087	PCS		2/23			P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0002594	PMID:15068978	PCS		5/6			P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0005563	OMIM:137920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000074	OMIM:137920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0001080	PMID:15930087	PCS					P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0040270	OMIM:137920	IEA					P	HPO:skoehler[2019-04-18]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000093	PMID:15930087	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0100611	PMID:15930087	PCS		4/23			P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0001738	PMID:15068978	PCS		6/7			P	HPO:iea[2010-12-28]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000107	PMID:15930087	PCS		28/46			P	HPO:iea[2010-12-28];HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0004904	PMID:15068978	PCS	HP:0003581	10/13			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000047	OMIM:137920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000006	OMIM:137920	PCS					I	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0001997	PMID:15930087	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0003259	PMID:15068978	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0000787	OMIM:137920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0001952	PMID:15930087	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:137920	Renal cysts and diabetes syndrome		HP:0002149	PMID:15930087	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0002069	PMID:24439110	PCS		3/4			P	HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0010804	PMID:24439110	PCS		5/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000582	PMID:24439110	PCS		3/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0002540	PMID:24439110	PCS		4/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0001250	PMID:24439110	PCS		4/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0003155	PMID:24439110	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0001252	PMID:24439110	PCS		5/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0003196	PMID:24439110	PCS		5/5			P	HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0003593	PMID:24439110	PCS		5/5			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0032794	PMID:24439110	PCS		1/4			P	HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0033725	PMID:24439110	PCS		1/5			P	HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000316	PMID:24439110	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000219	PMID:24439110	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000455	PMID:24439110	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0001249	PMID:24439110	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0009748	PMID:24439110	PCS		4/5			P	HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0006118	PMID:24439110	PCS		0/5			P	HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0003763	PMID:24439110	PCS		3/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000175	PMID:24439110	PCS		2/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000252	PMID:24439110	PCS		3/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0006956	PMID:24439110	PCS		1/5			P	HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000431	PMID:24439110	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0001344	PMID:24439110	PCS		5/5			P	HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0001263	PMID:24439110	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0002194	PMID:24439110	PCS		5/5			P	HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0000007	PMID:24439110	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-15]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0001510	PMID:24439110	PCS		1/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:615716	Hyperphosphatasia with impaired intellectual development syndrome 4		HP:0004305	PMID:24439110	PCS		3/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-01-16]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0002751	PMID:18439547	PCS		4/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0002333	PMID:18439547	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0003202	PMID:18439547	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000044	PMID:18439547	PCS		5/5			P	HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000670	PMID:18439547	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000252	PMID:18439547	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0001596	PMID:18439547	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000771	PMID:18439547	PCS		4/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0004322	PMID:18439547	PCS		2/5			P	HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0003121	PMID:18439547	PCS		4/5			P	HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0002493	PMID:18439547	PCS		5/5			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0011734	PMID:18439547	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:6000745	PMID:18439547	PCS					P	HPO:probinson[2024-06-29]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0012506	PMID:18439547	PCS		1/1			P	HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0009487	PMID:18439547	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000668	PMID:18439547	PCS		3/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000007	PMID:18439547	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0003758	PMID:18439547	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000823	PMID:18439547	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0001249	PMID:18439547	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-11-12]
OMIM:612079	Alopecia, neurologic defects, and endocrinopathy syndrome		HP:0000995	OMIM:612079	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0004325	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0003577	PMID:8857020	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000252	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0002750	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0004322	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0030353	PMID:8857020	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0001270	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000407	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000938	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000508	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000007	PMID:8857020	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000736	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0008897	PMID:8857020	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000845	PMID:8857020	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0004209	PMID:8857020	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000752	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0001511	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0001249	PMID:8857020	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-11-25]
OMIM:608747	Insulin-Like growth factor I deficiency		HP:0000347	PMID:8857020	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:617667	Fraser syndrome 3		HP:0001562	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0010958	PMID:22510445	PCS		2/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0000046	PMID:22510445	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0002101	PMID:22510445	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0001541	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0005343	PMID:22510445	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0001790	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0012725	PMID:22510445	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0034217	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0100682	PMID:22510445	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0012300	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0034198	PMID:22510445	PCS		3/3			C	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0003826	PMID:22510445	PCS		2/3			C	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0000007	PMID:22510445	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0000238	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0000444	PMID:22510445	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0001126	PMID:22510445	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0008736	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0000369	PMID:22510445	PCS		1/1			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0000347	PMID:22510445	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:617667	Fraser syndrome 3		HP:0020206	PMID:22510445	PCS		1/3			P	HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0001831	PMID:22510445	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:617667	Fraser syndrome 3		HP:0000445	PMID:22510445	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:192350	Vater associationvacterl association, included		HP:0001199	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002023	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002144	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001195	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000086	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002085	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001508	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001629	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000239	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001669	OMIM:192350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001602	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0008897	OMIM:192350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192350	Vater associationvacterl association, included		HP:0003745	OMIM:192350	IEA					I	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001643	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002414	OMIM:192350	TAS					P	HPO:skoehler[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0003468	OMIM:192350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002974	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000110	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002575	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000076	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000453	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000772	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002650	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002032	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000074	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0010479	OMIM:192350	TAS					P	HPO:skoehler[2014-01-28]
OMIM:192350	Vater associationvacterl association, included		HP:0100258	OMIM:192350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001739	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001636	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000766	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001159	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0001511	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000047	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0009778	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0002984	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0003974	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000126	OMIM:192350	IEA					P	HPO:iea[2009-02-17]
OMIM:192350	Vater associationvacterl association, included		HP:0000104	OMIM:192350	TAS					P	HPO:skoehler[2013-04-18]
OMIM:601005	Timothy syndrome		HP:0002045	PMID:15454078	PCS		5/17			P	HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001250	PMID:15454078	PCS		3/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001195	PMID:15454078	PCS		2/17			P	HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001252	PMID:15454078	PCS		7/17			P	HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0012725	PMID:15454078	PCS		17/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0002719	PMID:15454078	PCS		8/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001629	PMID:15454078	PCS		3/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0000717	PMID:15454078	PCS		10/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001943	PMID:15454078	PCS		7/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0000219	PMID:15454078	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001643	PMID:15454078	PCS		10/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0000311	PMID:15454078	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001249	PMID:15454078	PCS		4/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0004756	PMID:15454078	PCS		12/17			P	HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001662	PMID:15454078	PCS		16/17			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001640	PMID:15454078	PCS		6/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001263	PMID:15454078	PCS		4/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0000691	PMID:15454078	PCS		17/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0002092	PMID:15454078	PCS		3/17			P	HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0002090	PMID:15454078	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0005280	PMID:15454078	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0012387	PMID:15454078	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001636	PMID:15454078	PCS		1/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0000821	PMID:15454078	PCS		2/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001657	PMID:15454078	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0002901	PMID:15454078	PCS		6/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001678	PMID:15454078	PCS		16/17			P	HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0000006	PMID:15454078	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001655	PMID:15454078	PCS		5/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:601005	Timothy syndrome		HP:0001699	OMIM:601005	IEA					P	HPO:iea[2009-02-17]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000286	PMID:26340335	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0003577	OMIM:616579	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0010804	PMID:26340335	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000582	PMID:26340335	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000486	PMID:26340335	PCS		2/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002188	PMID:26340335	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000540	PMID:26340335	PCS		4/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002066	PMID:26340335	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001252	PMID:26340335	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002020	PMID:26340335	PCS		2/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0003593	PMID:26340335	PCS		1/5			C	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001270	PMID:26340335	PCS		5/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0012444	PMID:26340335	PCS		1/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000733	PMID:26340335	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000219	PMID:26340335	PCS		4/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000218	PMID:26340335	PCS		4/4			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002558	PMID:25533962	PCS		1/2			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001249	PMID:25533962;PMID:26340335	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-09];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0007328	PMID:26340335	PCS		4/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0003623	PMID:26340335	PCS		4/5			C	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000297	PMID:26340335	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001540	PMID:25533962	PCS		1/2			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002311	PMID:25533962	PCS		1/2			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000252	PMID:26340335	PCS		2/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001344	PMID:26340335	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002870	PMID:25533962	PCS		1/2			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000750	PMID:26340335	PCS		5/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000232	PMID:26340335	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000276	PMID:26340335	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0031936	PMID:26340335	PCS		5/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0011968	PMID:26340335	PCS	HP:0003623	4/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001382	PMID:25533962;PMID:26340335	PCS		3/7			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000194	PMID:26340335	PCS		4/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001260	PMID:26340335	PCS		3/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001263	PMID:25533962	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0100025	PMID:26340335	PCS		5/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001537	PMID:26340335	PCS		2/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000307	PMID:26340335	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002307	PMID:26340335	PCS		4/5			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0002205	PMID:26340335	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0001357	PMID:25533962	PCS		1/2			P	HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000322	PMID:26340335	PCS		5/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000006	PMID:25533962	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-09]
OMIM:616579	Intellectual developmental disorder, autosomal dominant 40		HP:0000369	PMID:26340335	PCS		3/5			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-06-09]
OMIM:300852	Intellectual developmental disorder, X-linked 88		HP:0001250	OMIM:300852	TAS		5/9			P	HPO:probinson[2013-09-14]
OMIM:300852	Intellectual developmental disorder, X-linked 88		HP:0001263	OMIM:300852	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300852	Intellectual developmental disorder, X-linked 88		HP:0000717	OMIM:300852	TAS		2/9			P	HPO:probinson[2013-09-14]
OMIM:300852	Intellectual developmental disorder, X-linked 88		HP:0001417	OMIM:300852	TAS					I	HPO:probinson[2013-01-12]
OMIM:300852	Intellectual developmental disorder, X-linked 88		HP:0001249	OMIM:300852	TAS					P	HPO:probinson[2013-09-14]
OMIM:268250	Rhizomelic syndrome		HP:0000252	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0008905	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0004322	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0000260	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0002827	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0000007	OMIM:268250	IEA					I	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0009611	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0001642	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0009943	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:268250	Rhizomelic syndrome		HP:0000347	OMIM:268250	IEA					P	HPO:iea[2009-02-17]
OMIM:604169	Left ventricular noncompaction 1		HP:0003577	PMID:11238270	PCS		5/6			C	HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0011705	PMID:29118297	PCS		1/1			P	HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0003581	PMID:11238270	PCS		1/6			C	HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0012817	PMID:29118297	PCS		1/1			P	HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0005110	OMIM:604169	TAS					P	HPO:skoehler[2013-05-03]
OMIM:604169	Left ventricular noncompaction 1		HP:0030682	PMID:29118297;PMID:11238270	PCS		7/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0004383	PMID:11238270	PCS		1/6			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0011664	PMID:11238270	PCS					P	HPO:probinson[2015-07-22];HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0001629	PMID:11238270	PCS		5/6			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0011462	PMID:29118297	PCS		1/1			C	HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0031352	PMID:29118297	PCS		1/1			P	HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0001635	OMIM:604169	TAS					P	HPO:skoehler[2013-05-03]
OMIM:604169	Left ventricular noncompaction 1		HP:0001712	PMID:11238270	TAS					P	HPO:probinson[2013-01-09]
OMIM:604169	Left ventricular noncompaction 1		HP:0004308	PMID:11238270	TAS					P	HPO:probinson[2013-02-23]
OMIM:604169	Left ventricular noncompaction 1		HP:0001962	PMID:29118297	PCS		1/1			P	HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0001643	PMID:11238270	PCS		1/6			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-07-10]
OMIM:604169	Left ventricular noncompaction 1		HP:0001653	OMIM:604169	TAS					P	HPO:skoehler[2013-05-31]
OMIM:604169	Left ventricular noncompaction 1		HP:0000006	PMID:11238270	TAS					I	HPO:probinson[2013-02-23]
OMIM:604169	Left ventricular noncompaction 1		HP:0001645	OMIM:604169	TAS					P	HPO:skoehler[2013-05-03]
OMIM:601777	Cone-Rod dystrophy 6		HP:0007737	PMID:20517349	PCS		3/6			P	HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0000662	PMID:20517349	PCS		6/6			P	HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0012047	OMIM:601777	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601777	Cone-Rod dystrophy 6		HP:0000639	OMIM:601777	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601777	Cone-Rod dystrophy 6		HP:0011463	OMIM:601777	TAS					C	HPO:probinson[2014-05-24]
OMIM:601777	Cone-Rod dystrophy 6		HP:0000613	PMID:20517349	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0007663	PMID:20517349	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0000007	OMIM:601777	IEA					I	HPO:skoehler[2018-10-08]
OMIM:601777	Cone-Rod dystrophy 6		HP:0007641	PMID:20517349	PCS		6/6			P	HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0007994	OMIM:601777	TAS					P	HPO:probinson[2009-02-17]
OMIM:601777	Cone-Rod dystrophy 6		HP:0007675	OMIM:601777	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601777	Cone-Rod dystrophy 6		HP:0000548	PMID:20517349	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0007401	PMID:20517349;OMIM:601777	PCS		15/16			P	HPO:probinson[2022-09-27];HPO:skoehler[2018-10-08]
OMIM:601777	Cone-Rod dystrophy 6		HP:0007843	PMID:20517349	PCS		1/6			P	HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0000006	PMID:20517349	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-27]
OMIM:601777	Cone-Rod dystrophy 6		HP:0003831	OMIM:601777	IEA					I	HPO:skoehler[2018-10-08]
OMIM:601777	Cone-Rod dystrophy 6		HP:0000533	PMID:20517349	PCS		6/6			P	HPO:probinson[2022-09-27]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001254	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002465	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0003676	PMID:11349233	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000486	OMIM:618226	IEA		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001332	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001272	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001250	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001252	PMID:11349233	PCS		3/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001251	OMIM:618226	IEA		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002240	PMID:11349233	PCS		1/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0003593	OMIM:618226	IEA		2/3			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001290	OMIM:618226	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0012444	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0007183	PMID:11349233	PCS		1/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001508	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000639	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000737	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002415	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001942	PMID:11349233	PCS		2/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001347	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0003128	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0003623	PMID:11349233	PCS		1/3			C	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0008936	PMID:11349233	PCS		1/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000253	OMIM:618226	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002015	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000252	PMID:11349233	PCS		1/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0003487	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002376	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002013	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002572	PMID:11349233	PCS		1/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002352	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001263	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002151	PMID:11349233	PCS		3/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002490	PMID:11349233	PCS		3/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0011923	PMID:11349233	PCS		3/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002093	OMIM:618226	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000508	OMIM:618226	IEA		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000602	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000007	PMID:11349233	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0000648	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0001510	PMID:11349233	PCS		1/3			P	HPO:probinson[2023-03-06];HPO:probinson[2023-03-06]
OMIM:618226	Mitochondrial complex I deficiency, nuclear type 5		HP:0002104	OMIM:618226	IEA		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-06]
OMIM:617115	Peeling skin syndrome 5		HP:0040189	PMID:27476651	PCS		7/7			P	HPO:probinson[2023-02-26]
OMIM:617115	Peeling skin syndrome 5		HP:0003593	PMID:27476651	PCS		7/7			C	HPO:probinson[2023-02-26]
OMIM:617115	Peeling skin syndrome 5		HP:0025092	PMID:27476651	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617115	Peeling skin syndrome 5		HP:0000007	PMID:27476651	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617115	Peeling skin syndrome 5		HP:0000962	PMID:27476651	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0031319	PMID:30715372	PCS		2/2			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0001670	PMID:30715372	PCS		3/8			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0002094	PMID:30715372	PCS		5/7			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0034532	PMID:30715372	PCS		2/2			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0031656	PMID:30715372	PCS		4/8			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0034386	PMID:30715372	PCS		5/7			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0011462	PMID:30715372	PCS		5/5			C	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0000007	PMID:30715372	PCS					I	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0001962	PMID:30715372	PCS		5/7			P	HPO:probinson[2023-06-16];HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0001324	PMID:30715372	PCS		0/8			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0001653	PMID:30715372	PCS		3/8			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0001645	PMID:30715372	PCS		3/11			P	HPO:probinson[2023-06-16]
OMIM:620236	Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies		HP:0032092	PMID:30715372	PCS		3/8			P	HPO:probinson[2023-06-16];HPO:probinson[2023-06-16]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000341	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0030799	PMID:32442410	PCS		2/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000263	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0001751	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000160	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0030431	PMID:32442410	PCS		3/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0003593	PMID:32442410	PCS					C	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0012745	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0010526	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000316	PMID:32442410	PCS		2/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000579	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000218	PMID:32442410	PCS		2/19			P	HPO:probinson[2020-09-10];HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0001007	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0001249	PMID:32442410	PCS		18/19			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0001166	PMID:32442410	PCS		2/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0001540	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000176	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0030820	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000574	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000431	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0009729	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000276	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0001263	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0003186	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000826	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000407	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000729	PMID:32442410	PCS		4/19			P	HPO:probinson[2022-08-27]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0500093	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000448	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0001537	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000348	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0004209	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000400	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0007018	PMID:32442410	PCS		10/19			P	HPO:probinson[2022-08-27]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000006	PMID:32442410	PCS					I	HPO:probinson[2020-09-10];HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000369	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000347	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000325	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:618971	Tolchin-Le Caignec syndrome		HP:0000269	PMID:32442410	PCS		1/19			P	HPO:probinson[2020-09-10]
OMIM:616784	Joubert syndrome 26		HP:0001320	PMID:26714646	PCS		3/3			P	HPO:probinson[2021-02-01]
OMIM:616784	Joubert syndrome 26		HP:0000054	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0000175	PMID:26714646	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:616784	Joubert syndrome 26		HP:0003577	PMID:26714646	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:616784	Joubert syndrome 26		HP:0000871	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0004322	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0000463	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0001263	PMID:26714646	PCS		3/3			P	HPO:probinson[2017-06-17];HPO:probinson[2021-02-01]
OMIM:616784	Joubert syndrome 26		HP:0001290	PMID:26714646	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:616784	Joubert syndrome 26		HP:0410030	PMID:26714646	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-01]
OMIM:616784	Joubert syndrome 26		HP:0011787	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0000639	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0000508	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0000316	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0000007	PMID:26714646	PCS					I	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0000824	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0002007	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:616784	Joubert syndrome 26		HP:0002788	PMID:26714646	PCS					P	HPO:probinson[2017-06-17]
OMIM:613824	Nephronophthisis 9		HP:0003774	PMID:18199800	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24];HPO:probinson[2024-03-14]
OMIM:613824	Nephronophthisis 9		HP:0001959	PMID:18199800	PCS		3/3			P	HPO:probinson[2024-03-14]
OMIM:613824	Nephronophthisis 9		HP:0001903	PMID:18199800	PCS		3/3			P	HPO:probinson[2024-03-14]
OMIM:613824	Nephronophthisis 9		HP:0000007	PMID:18199800	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:613824	Nephronophthisis 9		HP:0000090	PMID:18199800	PCS		3/3			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24];HPO:probinson[2024-03-14]
OMIM:613824	Nephronophthisis 9		HP:0000546	PMID:18199800	PCS		1/3			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24];HPO:probinson[2024-03-14]
OMIM:613824	Nephronophthisis 9		HP:0008897	PMID:18199800	PCS		3/3			P	HPO:probinson[2024-03-14]
OMIM:613824	Nephronophthisis 9		HP:0000103	PMID:18199800	PCS		3/3			P	HPO:probinson[2024-03-14]
OMIM:613824	Nephronophthisis 9		HP:0004734	PMID:18199800	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:612284	Meckel syndrome, type 6		HP:0002323	PMID:18513680	PCS	HP:0003577	2/11			P	HPO:skoehler[2013-01-10];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0000175	PMID:18513680	PCS	HP:0003577	2/4			P	HPO:skoehler[2013-01-10];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0002089	PMID:18513680	PCS		6/6			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0001762	PMID:18513680	PCS	HP:0003577	7/7			P	HPO:skoehler[2013-01-10];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0006706	PMID:18513680	PCS	HP:0003577	7/7			P	HPO:skoehler[2013-01-10];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0001162	PMID:18513680	PCS		8/10			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0001395	PMID:18513680	PCS		7/7			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0002085	PMID:18513680	PCS	HP:0003577	11/11			P	HPO:skoehler[2013-01-10];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0000085	PMID:18513680	PCS		1/11			P	HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0011467	PMID:18513680	PCS		1/11			P	HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0010477	PMID:18513680	PCS		1/11			P	HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0033183	PMID:18513680	PCS		1/11			P	HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0001408	OMIM:612284	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612284	Meckel syndrome, type 6		HP:0011461	PMID:18513680	PCS		11/11			C	HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0000107	PMID:18513680	PCS	HP:0003577	11/11			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0000007	PMID:18513680	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0000238	PMID:18513680	PCS		1/11			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0001407	PMID:18513680	PCS		7/7			P	HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0000812	OMIM:612284	IEA	HP:0003577	HP:0040283			P	HPO:skoehler[2013-01-10]
OMIM:612284	Meckel syndrome, type 6		HP:0001830	PMID:18513680	PCS		10/10			P	HPO:probinson[2022-03-26]
OMIM:612284	Meckel syndrome, type 6		HP:0000204	PMID:18513680	PCS	HP:0003577	2/4			P	HPO:skoehler[2013-01-10];HPO:probinson[2022-03-26]
OMIM:123570	Cryptophthalmos, unilateral or bilateral, isolated		HP:0000568	OMIM:123570	IEA					P	HPO:iea[2009-02-17]
OMIM:123570	Cryptophthalmos, unilateral or bilateral, isolated		HP:0000007	PMID:30802441	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2020-07-19]
OMIM:123570	Cryptophthalmos, unilateral or bilateral, isolated		HP:0009755	OMIM:123570	IEA					P	HPO:iea[2009-02-17]
OMIM:123570	Cryptophthalmos, unilateral or bilateral, isolated		HP:0001126	PMID:30802441	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-07-19]
OMIM:123570	Cryptophthalmos, unilateral or bilateral, isolated		HP:0000501	OMIM:123570	IEA					P	HPO:iea[2009-02-17]
OMIM:602097	Usher syndrome, type IE		HP:0001284	OMIM:602097	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602097	Usher syndrome, type IE		HP:0000007	OMIM:602097	IEA					I	HPO:iea[2009-02-17]
OMIM:602097	Usher syndrome, type IE		HP:0000510	OMIM:602097	IEA					P	HPO:iea[2009-02-17]
OMIM:602097	Usher syndrome, type IE		HP:0008568	OMIM:602097	IEA					P	HPO:iea[2009-02-17]
OMIM:602097	Usher syndrome, type IE		HP:0008527	OMIM:602097	IEA					P	HPO:iea[2009-02-17]
OMIM:106900	ANONYCHIA-ECTRODACTYLY		HP:0000968	OMIM:106900	IEA					P	HPO:iea[2009-02-17]
OMIM:106900	ANONYCHIA-ECTRODACTYLY		HP:0010048	OMIM:106900	IEA					P	HPO:iea[2009-02-17]
OMIM:106900	ANONYCHIA-ECTRODACTYLY		HP:0001171	OMIM:106900	IEA					P	HPO:iea[2009-02-17]
OMIM:106900	ANONYCHIA-ECTRODACTYLY		HP:0000006	OMIM:106900	IEA					I	HPO:iea[2009-02-17]
OMIM:106900	ANONYCHIA-ECTRODACTYLY		HP:0001798	OMIM:106900	IEA					P	HPO:iea[2009-02-17]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0031318	OMIM:600858	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0031628	PMID:11371514	PCS		3/8			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001670	OMIM:600858	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0005110	PMID:11371514	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0005165	PMID:15673802	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0011713	PMID:11371514	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001639	PMID:11371514;PMID:15673802	PCS		6/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001716	PMID:11371514	PCS		2/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001635	PMID:11371514	PCS		4/8			P	HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0004309	PMID:11371514	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0100749	PMID:11371514	PCS		1/8			P	HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001962	PMID:11371514	PCS					P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0006677	PMID:11371514	PCS		4/5			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001279	PMID:11371514	PCS		1/8			P	HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0000006	PMID:11371514	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001678	PMID:11371514	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-03]
OMIM:600858	Cardiomyopathy, familial hypertrophic, 6		HP:0001688	OMIM:600858	TAS					P	HPO:skoehler[2012-10-17]
OMIM:620550	Optic atrophy 14		HP:0001133	PMID:33632269	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:620550	Optic atrophy 14		HP:0003596	PMID:33632269	PCS		2/2			C	HPO:probinson[2024-03-08]
OMIM:620550	Optic atrophy 14		HP:0007663	PMID:33632269	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:620550	Optic atrophy 14		HP:0000543	PMID:33632269	PCS		2/2			P	HPO:probinson[2024-03-08]
OMIM:620550	Optic atrophy 14		HP:0000006	PMID:33632269	PCS					I	HPO:probinson[2024-03-08]
OMIM:212067	Congenital disorder of glycosylation, type I/IIx		HP:0011097	OMIM:212067	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212067	Congenital disorder of glycosylation, type I/IIx		HP:0001000	OMIM:212067	IEA					P	HPO:iea[2009-02-17]
OMIM:212067	Congenital disorder of glycosylation, type I/IIx		HP:0001250	OMIM:212067	IEA					P	HPO:iea[2009-02-17]
OMIM:212067	Congenital disorder of glycosylation, type I/IIx		HP:0001939	OMIM:212067	IEA					P	HPO:iea[2009-02-17]
OMIM:212067	Congenital disorder of glycosylation, type I/IIx		HP:0000007	OMIM:212067	IEA					I	HPO:iea[2009-02-17]
OMIM:212067	Congenital disorder of glycosylation, type I/IIx		HP:0012469	OMIM:212067	TAS					P	HPO:skoehler[2013-11-28]
OMIM:614839	Hypogonadotropic hypogonadism 10 with or without anosmia		HP:0000044	PMID:19079066	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-23]
OMIM:614839	Hypogonadotropic hypogonadism 10 with or without anosmia		HP:0030344	PMID:19079066	PCS		8/8			P	HPO:probinson[2023-02-23]
OMIM:614839	Hypogonadotropic hypogonadism 10 with or without anosmia		HP:0030341	PMID:19079066	PCS		2/8			P	HPO:probinson[2023-02-23]
OMIM:614839	Hypogonadotropic hypogonadism 10 with or without anosmia		HP:0000007	PMID:19079066	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-02-23]
OMIM:614839	Hypogonadotropic hypogonadism 10 with or without anosmia		HP:0000458	OMIM:614839	TAS		HP:0040283			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-23]
OMIM:614839	Hypogonadotropic hypogonadism 10 with or without anosmia		HP:0040171	PMID:19079066	PCS		2/2	MALE		P	HPO:probinson[2023-02-23]
OMIM:614839	Hypogonadotropic hypogonadism 10 with or without anosmia		HP:0000786	PMID:19079066	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-23]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0000396	PMID:27503514	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0031229	PMID:27503514	PCS		3/3			P	HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0000175	PMID:18394579;PMID:27503514	PCS		3/6			P	HPO:probinson[2021-07-13];HPO:probinson[2009-02-17];HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0003577	PMID:18394579	PCS		3/3			C	HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0008551	PMID:18394579;PMID:27503514	PCS		6/6			P	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13];HPO:probinson[2009-02-17];HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0000007	PMID:18394579	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0000410	PMID:18394579	PCS		3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0000006	PMID:27503514	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2021-07-13]
OMIM:612290	Microtia, hearing impairment, and cleft palate		HP:0000402	PMID:18394579;PMID:27503514	PCS		3/6			P	HPO:probinson[2021-07-13]
OMIM:602083	Usher syndrome, type IF		HP:0003577	PMID:11398101	PCS		7/7			C	HPO:probinson[2022-03-27]
OMIM:602083	Usher syndrome, type IF		HP:0001751	PMID:18719945	PCS		7/8			P	HPO:probinson[2022-03-27]
OMIM:602083	Usher syndrome, type IF		HP:0031629	PMID:18719945	PCS		7/8			P	HPO:probinson[2022-03-27]
OMIM:602083	Usher syndrome, type IF		HP:0000007	PMID:11398101	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-27]
OMIM:602083	Usher syndrome, type IF		HP:0001270	PMID:18719945	PCS		1/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-27]
OMIM:602083	Usher syndrome, type IF		HP:0000510	PMID:11398101;PMID:18719945	PCS		14/15			P	HPO:probinson[2022-03-27];HPO:probinson[2009-02-17];HPO:probinson[2022-03-27]
OMIM:602083	Usher syndrome, type IF		HP:0008527	PMID:11398101;PMID:18719945	PCS		15/15			P	HPO:probinson[2022-03-27];HPO:probinson[2009-02-17];HPO:probinson[2022-03-27]
OMIM:613830	Night blindness, congenital stationary, type 1D		HP:0011463	PMID:20850105	PCS		5/5			C	HPO:probinson[2023-01-20]
OMIM:613830	Night blindness, congenital stationary, type 1D		HP:0000580	PMID:20850105	PCS		0/4			P	HPO:probinson[2023-01-20]
OMIM:613830	Night blindness, congenital stationary, type 1D		HP:0000007	PMID:20850105	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:613830	Night blindness, congenital stationary, type 1D		HP:0007642	PMID:20850105	PCS		5/5			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-01-20]
OMIM:613830	Night blindness, congenital stationary, type 1D		HP:0007401	PMID:20850105	PCS		0/4			P	HPO:probinson[2023-01-20]
OMIM:613830	Night blindness, congenital stationary, type 1D		HP:0007843	PMID:20850105	PCS		0/4			P	HPO:probinson[2023-01-20]
OMIM:614187	Hypertelorism, preauricular sinus, punctal pits, and deafness		HP:0004467	OMIM:614187	TAS				HP:0012832	P	HPO:skoehler[2014-11-26]
OMIM:614187	Hypertelorism, preauricular sinus, punctal pits, and deafness		HP:0000365	OMIM:614187	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614187	Hypertelorism, preauricular sinus, punctal pits, and deafness		HP:0000316	OMIM:614187	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614187	Hypertelorism, preauricular sinus, punctal pits, and deafness		HP:0000579	OMIM:614187	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614187	Hypertelorism, preauricular sinus, punctal pits, and deafness		HP:0000006	OMIM:614187	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614187	Hypertelorism, preauricular sinus, punctal pits, and deafness		HP:0000049	OMIM:614187	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259270	Osteodysplasty, precocious, of danks, mayne, and kozlowski		HP:0009381	OMIM:259270	PCS					P	HPO:probinson[2012-03-16]
OMIM:259270	Osteodysplasty, precocious, of danks, mayne, and kozlowski		HP:0011314	OMIM:259270	PCS					P	HPO:probinson[2012-03-16]
OMIM:259270	Osteodysplasty, precocious, of danks, mayne, and kozlowski		HP:0000007	OMIM:259270	IEA					I	HPO:iea[2009-02-17]
OMIM:259270	Osteodysplasty, precocious, of danks, mayne, and kozlowski		HP:0002205	OMIM:259270	PCS					P	HPO:probinson[2012-03-16]
OMIM:259270	Osteodysplasty, precocious, of danks, mayne, and kozlowski		HP:0001510	OMIM:259270	IEA					P	HPO:iea[2009-02-17]
OMIM:259270	Osteodysplasty, precocious, of danks, mayne, and kozlowski		HP:0002644	OMIM:259270	PCS					P	HPO:probinson[2009-02-17]
OMIM:259270	Osteodysplasty, precocious, of danks, mayne, and kozlowski		HP:0001831	OMIM:259270	PCS					P	HPO:probinson[2012-03-16]
OMIM:620222	Spermatogenic failure 80		HP:0032560	PMID:34169321	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620222	Spermatogenic failure 80		HP:0034011	PMID:34169321	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620222	Spermatogenic failure 80		HP:0003251	PMID:34169321	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620222	Spermatogenic failure 80		HP:0011462	PMID:34169321	PCS		2/2			C	HPO:probinson[2023-06-10]
OMIM:620222	Spermatogenic failure 80		HP:0000007	PMID:34169321	PCS					I	HPO:probinson[2023-06-10]
OMIM:620222	Spermatogenic failure 80		HP:0032558	PMID:34169321	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620222	Spermatogenic failure 80		HP:0000798	PMID:34169321	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:620222	Spermatogenic failure 80		HP:0032559	PMID:34169321	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0002078	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0002079	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0001310	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0001272	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0001260	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0001251	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0002061	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0002080	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0000639	OMIM:616948	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0000007	PMID:26157035	PCS					I	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0007256	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0002317	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0003677	OMIM:616948	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0001249	OMIM:616948	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616948	Spinocerebellar ataxia, autosomal recessive 22		HP:0001347	PMID:26157035	PCS					P	HPO:probinson[2017-06-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0003236	PMID:21388311	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0000750	PMID:21388311	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0001288	PMID:21388311	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0030046	PMID:21388311	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0003551	PMID:21388311	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0001263	PMID:21388311	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0003560	PMID:21388311	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0003391	OMIM:613818	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0011463	PMID:21388311	PCS		1/1			C	HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0002938	PMID:21388311	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0000007	PMID:21388311	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0002317	PMID:21388311	PCS	HP:0011463	1/1			P	HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0006466	PMID:21388311	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0003325	PMID:21388311	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:613818	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9		HP:0001249	PMID:21388311	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-25]
OMIM:618795	Juvenile arthritis		HP:0001894	PMID:25220867	PCS		13/13			P	HPO:probinson[2020-05-04]
OMIM:618795	Juvenile arthritis		HP:0033087	PMID:25220867	PCS		13/13			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618795	Juvenile arthritis		HP:0011463	PMID:25220867	PCS					C	HPO:probinson[2020-05-04]
OMIM:618795	Juvenile arthritis		HP:0003493	PMID:25220867	PCS		8/13			P	HPO:probinson[2020-05-04]
OMIM:618795	Juvenile arthritis		HP:0000007	PMID:25220867	PCS					I	HPO:probinson[2020-05-04];HPO:probinson[2020-05-04]
OMIM:618795	Juvenile arthritis		HP:0032323	PMID:25220867	PCS		13/13			P	HPO:probinson[2020-05-04]
OMIM:618795	Juvenile arthritis		HP:0000988	PMID:25220867	PCS					P	HPO:probinson[2020-05-04]
OMIM:618795	Juvenile arthritis		HP:0001974	PMID:25220867	PCS		13/13			P	HPO:probinson[2020-05-04]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0031506	PMID:16228000	PCS		4/4			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0002750	PMID:16228000	PCS		2/4			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0004322	PMID:16228000	PCS	HP:0003593	2/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0033077	PMID:16228000	PCS		4/4			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0032210	PMID:16228000	PCS		4/4			P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0000007	PMID:16228000	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0002925	PMID:16228000	PCS		4/4			P	HPO:probinson[2013-01-09];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0000821	PMID:16228000	PCS		0/4			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-08]
OMIM:609698	Thyroid hormone metabolism, abnormal		HP:0003623	PMID:16228000	PCS		1/1			C	HPO:probinson[2022-06-08]
OMIM:243200	Intracranial hypertension, idiopathic		HP:0001085	OMIM:243200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:243200	Intracranial hypertension, idiopathic		HP:0000822	OMIM:243200	TAS					P	HPO:skoehler[2010-06-20]
OMIM:243200	Intracranial hypertension, idiopathic		HP:0000007	OMIM:243200	TAS					I	HPO:skoehler[2009-02-17]
OMIM:243200	Intracranial hypertension, idiopathic		HP:0002516	OMIM:243200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:215720	Citrulline transport defect		HP:0001939	OMIM:215720	IEA					P	HPO:iea[2009-02-17]
OMIM:215720	Citrulline transport defect		HP:0000007	OMIM:215720	IEA					I	HPO:iea[2009-02-17]
OMIM:215720	Citrulline transport defect		HP:0001510	OMIM:215720	IEA					P	HPO:iea[2009-02-17]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0002751	PMID:14755468	PCS		2/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0007759	PMID:2229114	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0003467	PMID:14755468	PCS		1/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0004279	PMID:14755468	PCS		7/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0004322	PMID:14755468	PCS		7/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0430046	PMID:14755468	PCS		1/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0000470	PMID:14755468	PCS		3/4			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0040160	PMID:14755468	PCS		7/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0100864	PMID:14755468	PCS		7/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0000914	PMID:14755468	PCS		1/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0000926	PMID:14755468	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0008155	PMID:2229114	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0002857	PMID:14755468	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0000768	PMID:14755468	PCS		2/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0001763	PMID:14755468	PCS		2/7			P	HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0000006	PMID:14755468	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0001249	PMID:2229114	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:184095	Spondyloepiphyseal dysplasia, Maroteaux type		HP:0002655	PMID:14755468	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:306990	Holoprosencephaly with fetal akinesia/hypokinesia sequence		HP:0000252	OMIM:306990	IEA					P	HPO:iea[2009-02-17]
OMIM:306990	Holoprosencephaly with fetal akinesia/hypokinesia sequence		HP:0001360	OMIM:306990	IEA					P	HPO:iea[2009-02-17]
OMIM:306990	Holoprosencephaly with fetal akinesia/hypokinesia sequence		HP:0002828	OMIM:306990	IEA					P	HPO:skoehler[2010-06-20]
OMIM:306990	Holoprosencephaly with fetal akinesia/hypokinesia sequence		HP:0001558	OMIM:306990	IEA					P	HPO:iea[2009-02-17]
OMIM:306990	Holoprosencephaly with fetal akinesia/hypokinesia sequence		HP:0001417	OMIM:306990	IEA					I	HPO:iea[2009-02-17]
OMIM:306990	Holoprosencephaly with fetal akinesia/hypokinesia sequence		HP:0001989	OMIM:306990	TAS					P	HPO:probinson[2013-08-13]
OMIM:306990	Holoprosencephaly with fetal akinesia/hypokinesia sequence		HP:0001511	OMIM:306990	IEA					P	HPO:iea[2009-02-17]
OMIM:174400	Polydactyly, preaxial I		HP:0001177	OMIM:174400	TAS					P	HPO:iea[2009-02-17]
OMIM:174400	Polydactyly, preaxial I		HP:0005895	OMIM:174400	TAS					P	HPO:iea[2009-02-17]
OMIM:174400	Polydactyly, preaxial I		HP:0000007	OMIM:174400	TAS					I	HPO:skoehler[2019-09-07]
OMIM:174400	Polydactyly, preaxial I		HP:0009944	OMIM:174400	TAS					P	HPO:skoehler[2019-09-07]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0003124	OMIM:301033	TAS					P	HPO:probinson[2020-07-24]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0033075	PMID:27603907	PCS					P	HPO:probinson[2020-10-13]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0000869	OMIM:301033	TAS					P	HPO:probinson[2020-07-24]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0033078	PMID:27603907	PCS		7/17			P	HPO:probinson[2020-10-13]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0003593	PMID:27603907	PCS		6/8			C	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0001417	PMID:27603907	PCS					I	HPO:probinson[2020-07-24]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0000256	OMIM:301033	TAS					P	HPO:probinson[2020-07-24]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0002019	OMIM:301033	TAS					P	HPO:probinson[2020-07-24]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0007018	OMIM:301033	TAS					P	HPO:probinson[2020-07-24]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0011787	PMID:27603907	PCS					P	HPO:probinson[2020-07-24]
OMIM:301033	Hypothyroidism, congenital, nongoitrous, 8		HP:0031987	OMIM:301033	TAS					P	HPO:probinson[2020-07-24]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0001374	OMIM:255310	IEA					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0003577	OMIM:255310	IEA					C	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0010628	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0001508	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0003828	OMIM:255310	TAS					M	HPO:skoehler[2012-10-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0032341	OMIM:255310	IEA					P	HPO:skoehler[2019-04-18]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0002938	OMIM:255310	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0000218	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0003701	OMIM:255310	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0001644	OMIM:255310	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0000275	OMIM:255310	TAS					P	HPO:probinson[2012-05-01]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0002015	OMIM:255310	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0003324	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0003687	OMIM:255310	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0002650	OMIM:255310	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0000276	OMIM:255310	TAS					P	HPO:probinson[2012-05-01]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0001283	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0003121	OMIM:255310	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0011968	OMIM:255310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0002093	OMIM:255310	TAS					P	HPO:skoehler[2010-06-20]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0000508	OMIM:255310	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0000602	OMIM:255310	TAS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0001558	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0000007	OMIM:255310	TAS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0001319	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0002747	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0000006	OMIM:255310	IEA					I	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0001612	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:255310	Myopathy, congenital, with fiber-type disproportion		HP:0003755	OMIM:255310	IEA					P	HPO:iea[2009-02-17]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0030853	PMID:31959991	PCS		0/9			P	HPO:probinson[2020-05-06];HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0002110	PMID:31959991	PCS		9/9			P	HPO:probinson[2020-05-06];HPO:probinson[2020-05-06];HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0032341	PMID:31959991	PCS		5/7			P	HPO:probinson[2020-10-13]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0032342	PMID:31959991	PCS		6/7			P	HPO:probinson[2020-10-13]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0003593	PMID:31959991	PCS		7/9			C	HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0033036	PMID:31959991	PCS		0/4			P	HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0000007	PMID:31959991	PCS					I	HPO:probinson[2020-05-06];HPO:probinson[2020-05-06];HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0011108	PMID:31959991	PCS		8/9			P	HPO:probinson[2020-05-06];HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0040128	PMID:31959991	PCS		0/5			P	HPO:probinson[2020-05-06];HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0000388	PMID:31959991	PCS	HP:0011463	2/9			P	HPO:probinson[2020-05-06];HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0002643	PMID:31959991	PCS	HP:0003623	2/9			P	HPO:probinson[2020-05-06];HPO:probinson[2020-05-06];HPO:probinson[2024-03-16]
OMIM:618781	Ciliary dyskinesia, primary, 44		HP:0003623	PMID:31959991	PCS		2/9			C	HPO:probinson[2024-03-16]
OMIM:170100	Prolidase deficiency		HP:0009937	PMID:18340504	PCS					P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0006528	PMID:19308961	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-12]
OMIM:170100	Prolidase deficiency		HP:0002162	PMID:18340504	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0003196	PMID:19308961	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0002240	PMID:16470701	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0010702	PMID:16470701;PMID:18340504	PCS		13/14			P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0002719	PMID:16470701	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0001508	PMID:16470701	PCS		2/4			P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0001903	PMID:16470701	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0011463	PMID:18340504	PCS					C	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0011342	PMID:16470701	PCS		2/4			P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0011220	PMID:16470701	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0011120	PMID:18340504	PCS					P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0000316	PMID:16470701	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0007489	OMIM:170100	IEA					P	HPO:iea[2009-02-17]
OMIM:170100	Prolidase deficiency		HP:0006532	PMID:16470701	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0000218	PMID:18340504	PCS					P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0006579	PMID:16470701	PCS		4/4			P	HPO:skoehler[2013-06-03];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0001744	PMID:16470701;PMID:19308961	PCS		15/23			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0200042	PMID:16470701;PMID:18340504	PCS		14/14			P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0031956	PMID:16470701	PCS		4/4		HP:0012825	P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0002373	PMID:16470701	PCS	HP:0003593	2/4			P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0002099	PMID:16470701;PMID:19308961	PCS		7/23			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0001263	PMID:19308961	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0005280	PMID:16470701	IEA		4/4			P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:6000828	PMID:12384772	PCS		5/5			P	HPO:probinson[2024-08-03]
OMIM:170100	Prolidase deficiency		HP:0033187	PMID:19308961	PCS					P	HPO:probinson[2020-10-12]
OMIM:170100	Prolidase deficiency		HP:0007473	PMID:19308961	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0000508	OMIM:170100	IEA					P	HPO:iea[2009-02-17]
OMIM:170100	Prolidase deficiency		HP:0000007	PMID:19308961	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0000964	PMID:16470701	PCS		4/4			P	HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0000967	PMID:16470701	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0002725	PMID:19308961	PCS		2/19			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0000520	PMID:16470701	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-30];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0001873	PMID:16470701	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-30]
OMIM:170100	Prolidase deficiency		HP:0000347	PMID:18340504	PCS					P	HPO:probinson[2020-09-30]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0001410	PMID:27132592	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0001252	PMID:27132592	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0002020	PMID:27132592	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0032653	PMID:27132592	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0031964	PMID:27132592	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0001508	PMID:27132592	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0002878	PMID:27132592	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0008314	PMID:27132592	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0001522	PMID:27132592	PCS		2/2			C	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:6000182	PMID:27132592	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0003688	PMID:27132592	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0003623	PMID:27132592	PCS		2/2			C	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0003128	PMID:27132592	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0003348	PMID:27132592	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0031956	PMID:27132592	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0003200	PMID:27132592	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0011968	PMID:27132592	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0011924	PMID:27132592	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0002033	PMID:27132592	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0002151	PMID:27132592	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0002490	PMID:27132592	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0030948	PMID:27132592	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0011923	PMID:27132592	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0000407	PMID:27132592	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0001712	PMID:27132592	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0000007	PMID:27132592	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0008347	PMID:27132592	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0002126	PMID:27132592	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:616974	Combined oxidative phosphorylation deficiency 30		HP:0006821	PMID:27132592	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-10]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0000253	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0001276	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0008936	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0002521	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0000232	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0001250	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0001263	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0005280	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0012110	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0100876	PMID:31538237	PCS					P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0007068	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0000007	PMID:31538237	PCS					I	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0000348	PMID:31538237	PCS					P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0001338	PMID:31538237	PCS					P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0200134	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0500149	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:618959	Epileptic encephalopathy, early infantile, 88		HP:0001510	PMID:31538237	PCS					P	HPO:probinson[2020-08-31]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0002069	PMID:39824192	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0004325	PMID:39824192	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001650	PMID:39824192	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000365	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001332	PMID:39824192	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001250	PMID:39824192	PCS		4/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001252	PMID:39824192	PCS		4/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0003196	PMID:39824192	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0030891	PMID:39824192	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0003593	PMID:39824192	PCS		7/14			C	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0004482	PMID:39824192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000718	PMID:39824192	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0011220	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000717	PMID:39824192	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000316	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0020045	PMID:39824192	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001249	PMID:39824192	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001344	PMID:39824192	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0031354	PMID:39824192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0031355	PMID:39824192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0100022	PMID:39824192	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0011451	PMID:39824192	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0011098	PMID:39824192	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000007	PMID:39824192	PCS					I	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0002307	PMID:39824192	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000405	PMID:39824192	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0004209	PMID:39824192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000322	PMID:39824192	PCS		3/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001336	PMID:39824192	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000445	PMID:39824192	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001276	PMID:39824192	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000463	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000540	PMID:39824192	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0002002	PMID:39824192	PCS		4/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0010863	PMID:39824192	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000733	PMID:39824192	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0012170	PMID:39824192	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0030084	PMID:39824192	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0012171	PMID:39824192	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000218	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0009765	PMID:39824192	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000256	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000431	PMID:39824192	PCS		2/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000750	PMID:39824192	PCS		1/2			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0031936	PMID:39824192	PCS		5/8			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0002376	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0003388	PMID:39824192	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0002013	PMID:39824192	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0002171	PMID:39824192	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0005280	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000749	PMID:39824192	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001518	PMID:39824192	PCS		5/7			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0011154	PMID:39824192	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0100716	PMID:39824192	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0001159	PMID:39824192	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0000664	PMID:39824192	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:621100	Intellectual developmental disorder, autosomal recessive 83		HP:0007018	PMID:39824192	PCS		2/5			P	ORCID:0000-0002-0736-9199[2025-09-28]
OMIM:236660	Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis		HP:0002751	OMIM:236660	IEA					P	HPO:skoehler[2015-12-30]
OMIM:236660	Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis		HP:0000098	OMIM:236660	IEA					P	HPO:iea[2009-02-17]
OMIM:236660	Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis		HP:0001382	OMIM:236660	IEA					P	HPO:iea[2009-02-17]
OMIM:236660	Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis		HP:0000007	OMIM:236660	IEA					I	HPO:iea[2009-02-17]
OMIM:236660	Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis		HP:0000238	OMIM:236660	IEA					P	HPO:iea[2009-02-17]
OMIM:236660	Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis		HP:0005619	OMIM:236660	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0002411	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0000651	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0002013	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0002321	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0002131	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0000360	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0001324	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0002018	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0002315	OMIM:606554	IEA					P	HPO:iea[2009-02-17]
OMIM:606554	Episodic ataxia, type 3		HP:0000006	OMIM:606554	IEA					I	HPO:iea[2009-02-17]
OMIM:619312	Radio-Tartaglia syndrome		HP:0004523	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000286	PMID:33596411	PCS		11/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000365	PMID:33596411	PCS		3/31			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001250	PMID:33596411	PCS		19/64			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001252	PMID:33596411	PCS		22/30			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002020	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002141	PMID:33596411	PCS		14/27			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001251	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000280	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000958	PMID:33596411	PCS		6/29			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0012471	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000718	PMID:33596411	PCS		11/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000316	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000678	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000637	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000278	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001763	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002019	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0009748	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001249	PMID:33596411	PCS		33/33			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001007	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002553	PMID:33596411	PCS		5/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000252	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000494	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000574	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001344	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000490	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001065	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001263	PMID:33596411	PCS		33/33			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000294	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001182	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0009890	PMID:33596411	PCS		5/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000729	PMID:33596411	PCS		18/28			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002705	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000527	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002307	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000405	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000322	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001337	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000369	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000006	PMID:33596411	PCS					I	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000341	PMID:33596411	PCS		6/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000582	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001792	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000343	PMID:33596411	PCS		7/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001156	PMID:33596411	PCS		5/30			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000463	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001274	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0005274	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002282	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001270	PMID:33596411	PCS		8/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001629	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000817	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000733	PMID:33596411	PCS		13/28			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000414	PMID:33596411	PCS		8/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000219	PMID:33596411	PCS		5/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000218	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0025116	PMID:33596411	PCS	HP:0011461	3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001028	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000154	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002015	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000431	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002650	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000750	PMID:33596411	PCS		9/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001761	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000276	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0045025	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0005280	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0100710	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000826	PMID:33596411	PCS		4/18			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000629	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000426	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000307	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000664	PMID:33596411	PCS		9/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0002007	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000300	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0007018	PMID:33596411	PCS		3/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0001513	PMID:33596411	PCS		2/32			P	HPO:probinson[2021-07-06]
OMIM:619312	Radio-Tartaglia syndrome		HP:0000347	PMID:33596411	PCS		4/32			P	HPO:probinson[2021-07-06]
OMIM:136800	Corneal dystrophy, fuchs endothelial, 1		HP:0007705	OMIM:136800	TAS					P	HPO:probinson[2011-02-10]
OMIM:136800	Corneal dystrophy, fuchs endothelial, 1		HP:0012040	OMIM:136800	TAS					P	HPO:probinson[2012-07-27]
OMIM:136800	Corneal dystrophy, fuchs endothelial, 1		HP:0001131	OMIM:136800	TAS					P	HPO:probinson[2009-02-17]
OMIM:136800	Corneal dystrophy, fuchs endothelial, 1		HP:0012038	OMIM:136800	TAS					P	HPO:probinson[2012-07-22]
OMIM:136800	Corneal dystrophy, fuchs endothelial, 1		HP:0000006	OMIM:136800	TAS					I	HPO:probinson[2009-02-17]
OMIM:136800	Corneal dystrophy, fuchs endothelial, 1		HP:0012039	OMIM:136800	TAS					P	HPO:probinson[2012-07-27]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000286	PMID:20186804	PCS		4/13			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001176	PMID:20186804	PCS		6/13			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002188	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000365	PMID:18505557	PCS		20%			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000486	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001250	PMID:20186804	PCS		4/13			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002020	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001290	PMID:20186804	PCS		4/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000718	PMID:20301377	PCS		25%			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000717	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2011-04-03];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000316	PMID:23758760	PCS		4/32			P	HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001800	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001643	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0003745	PMID:20301377	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001004	PMID:20186804;PMID:18505557	PCS		8/23			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000113	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000710	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0007328	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0003763	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001265	OMIM:606232	TAS	HP:0003623				P	HPO:skoehler[2012-11-26]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000252	PMID:20301377	PCS		HP:0040284			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000098	PMID:20301377	PCS		HP:0040281			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000574	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000331	OMIM:606232	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0011968	PMID:20186804	PCS	HP:0003623	5/12			P	HPO:skoehler[2012-11-26];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000293	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001382	PMID:23758760	PCS		8/32			P	HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000490	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001263	PMID:20186804;PMID:20301377	PCS		23/23			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0004691	PMID:18505557	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0100540	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0100658	PMID:18505557	PCS		10%			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000689	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000527	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0004209	PMID:18505557	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000966	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000400	PMID:20186804	PCS		9/13			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000960	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000006	PMID:23758760	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000687	PMID:23758760	PCS		6/32			P	HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000343	PMID:23758760;PMID:20301377	PCS		10/42			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002046	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001270	OMIM:606232	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002719	PMID:20186804	PCS		4/13			P	HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0100703	PMID:18505557	PCS		15%			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001629	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0100704	PMID:20301377	PCS		6%			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000817	PMID:18505557	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0100702	PMID:18505557	PCS		15%			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0011120	OMIM:606232	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002518	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000414	PMID:20186804	PCS		9/13			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000733	PMID:18505557	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002317	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002119	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000218	PMID:23758760;PMID:20301377	PCS		13/42			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000411	OMIM:606232	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000256	PMID:23758760	PCS		10/32			P	HPO:skoehler[2012-10-17];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000336	OMIM:606232	TAS					P	HPO:skoehler[2015-10-05]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000077	PMID:23758760	PCS		12/32			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002136	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000076	ISBN-13:978-0721606156	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000750	PMID:20186804	PCS		13/13			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000431	PMID:23758760;PMID:20301377	PCS		10/42			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0002572	PMID:18505557	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000272	PMID:20301377	PCS		HP:0040282			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000708	PMID:20186804;PMID:18505557	PCS		21/23			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0012760	PMID:18505557	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0100797	OMIM:606232	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000508	PMID:18505557	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0001319	PMID:20301377	PCS		HP:0040281			P	HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000307	PMID:20186804;PMID:23758760	PCS		10/45			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000268	PMID:23758760;PMID:20301377	PCS		13/42			P	HPO:probinson[2019-11-28];HPO:iea[2012-04-24];HPO:probinson[2019-11-28]
OMIM:606232	Phelan-Mcdermid syndrome		HP:0000347	PMID:23758760	PCS		4/32			P	HPO:probinson[2019-11-28]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0001363	OMIM:612247	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000453	OMIM:612247	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000316	OMIM:612247	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0011800	PMID:7493034	PCS		4/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-26]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000238	PMID:7493034	PCS		3/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-26]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000956	PMID:7493034	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000520	PMID:7493034	PCS		4/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-26]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000248	OMIM:612247	TAS					P	HPO:skoehler[2015-08-16]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000006	PMID:7493034	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-26]
OMIM:612247	Crouzon syndrome with acanthosis nigricans		HP:0000995	OMIM:612247	TAS					P	HPO:skoehler[2015-08-16]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0000571	PMID:22563501	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0003621	PMID:22563501	PCS		2/2			C	HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0002067	PMID:22563501	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0001300	OMIM:615528	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0001332	OMIM:615528	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0001250	OMIM:615528	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0002362	OMIM:615528	TAS					P	HPO:skoehler[2013-11-28]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0001260	PMID:22563501	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0002063	PMID:22563501	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0025387	PMID:22563501	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0002172	PMID:22563501	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0030904	PMID:22563501	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0100543	OMIM:615528	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0000738	OMIM:615528	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0002509	PMID:22563501	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0000338	PMID:22563501	PCS		2/2			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0007256	OMIM:615528	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0000007	PMID:22563501	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0002505	PMID:22563501	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0001257	OMIM:615528	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0001249	OMIM:615528	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0003677	OMIM:615528	TAS					C	HPO:skoehler[2017-07-13]
OMIM:615528	Parkinson disease 19a, juvenile-onset		HP:0003678	OMIM:615528	TAS					C	HPO:skoehler[2013-11-28]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0003774	PMID:20179356	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0001250	PMID:20179356	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0005583	PMID:20179356	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0000090	PMID:20179356	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0000092	PMID:20179356	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0006280	PMID:20179356	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0000407	PMID:20179356	PCS		2/5			P	HPO:skoehler[2014-05-04];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0100702	PMID:20179356	PCS		1/5			P	HPO:skoehler[2013-05-31];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0004719	PMID:20179356	PCS		5/5			P	HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0000822	PMID:20179356	PCS		3/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0030186	PMID:20179356	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0000007	PMID:20179356	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0001737	PMID:20179356	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0000108	PMID:20179356	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-13]
OMIM:613159	Nephronophthisis-Like nephropathy 1		HP:0001249	PMID:20179356	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-10-13]
OMIM:614622	Keratoconus 5		HP:0000563	OMIM:614622	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614622	Keratoconus 5		HP:0000006	OMIM:614622	TAS					I	HPO:skoehler[2012-10-17]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002267	PMID:9932959	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001276	OMIM:272750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002421	OMIM:272750	IEA					P	HPO:iea[2009-02-17]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001332	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0003495	PMID:9932959	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001250	OMIM:272750	IEA					P	HPO:iea[2009-02-17]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001252	PMID:9932959	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0003593	PMID:9932959	PCS		1/1			C	HPO:probinson[2023-02-26]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001290	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0032794	PMID:9932959	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0003470	OMIM:272750	IEA					P	HPO:iea[2009-02-17]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002180	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0000618	OMIM:272750	IEA					P	HPO:iea[2009-02-17]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002835	OMIM:272750	IEA					P	HPO:iea[2009-02-17]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001347	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0008936	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002476	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002059	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001263	PMID:9932959	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002371	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0001285	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0002072	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0000726	OMIM:272750	IEA					P	HPO:iea[2009-02-17]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0010780	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0007256	OMIM:272750	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0000007	PMID:1915858	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:272750	GM2-gangliosidosis, AB variant		HP:0000741	OMIM:272750	IEA					P	HPO:iea[2009-02-17]
OMIM:610444	Night blindness, congenital stationary, autosomal dominant 3		HP:0007642	PMID:8673138	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2023-02-26]
OMIM:610444	Night blindness, congenital stationary, autosomal dominant 3		HP:0000006	PMID:8673138	PCS					I	HPO:probinson[2013-02-28];HPO:probinson[2023-02-26]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0025386	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0003577	PMID:32639540	PCS		2/3			C	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000340	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000582	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000343	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0002365	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0001371	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0001250	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0002263	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0003593	PMID:32639540	PCS		1/3			C	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0010664	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000958	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0001629	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000319	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000437	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000316	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0002419	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000219	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0003429	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0001747	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0006610	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0007766	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0020206	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0001320	PMID:32639540	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0002510	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000431	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0031913	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0002870	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0002079	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0001321	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0002198	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0005484	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0011344	PMID:32639540	PCS		2/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0030724	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000007	PMID:32639540	PCS					I	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000300	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:619306	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia		HP:0000369	PMID:32639540	PCS		1/3			P	HPO:probinson[2021-07-04]
OMIM:601549	ALACRIMA		HP:0000584	OMIM:601549	IEA					P	HPO:iea[2009-02-17]
OMIM:601549	ALACRIMA		HP:0000613	OMIM:601549	IEA					P	HPO:iea[2009-02-17]
OMIM:601549	ALACRIMA		HP:0000007	OMIM:601549	IEA					I	HPO:iea[2009-02-17]
OMIM:601549	ALACRIMA		HP:0000522	OMIM:601549	IEA					P	HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0001265	OMIM:609115	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003236	OMIM:609115	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0008948	OMIM:609115	IEA					P	HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003198	OMIM:609115	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003581	PMID:24647604;OMIM:609115	PCS		20/20			C	HPO:probinson[2022-10-17];HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0000518	OMIM:609115	TAS					P	HPO:skoehler[2014-11-26]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003829	OMIM:609115	TAS					I	HPO:skoehler[2015-12-30]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003749	OMIM:609115	IEA					P	HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003805	OMIM:609115	TAS					P	HPO:skoehler[2014-11-26]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0008116	OMIM:609115	IEA					P	HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0006785	OMIM:609115	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003547	OMIM:609115	IEA					P	HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0006203	OMIM:609115	IEA					P	HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0000006	PMID:24647604	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-10-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0003677	OMIM:609115	IEA					C	HPO:iea[2009-02-17]
OMIM:609115	Limb-girdle muscular dystrophy, type 1G		HP:0008956	OMIM:609115	IEA					P	HPO:iea[2009-02-17]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000483	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001773	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000486	PMID:33864376	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000463	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001250	PMID:33864376	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000160	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001252	PMID:33864376	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001508	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0012471	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0011461	PMID:33864376	PCS		2/2			C	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000316	PMID:33864376	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0008872	PMID:33864376	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001566	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000377	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001347	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000577	PMID:33864376	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001562	PMID:33864376	PCS	HP:0011461	1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0002553	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000154	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000490	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0011344	PMID:33864376	PCS		2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0005280	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0005180	PMID:33864376	PCS		1/2		HP:0012825	P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0011451	PMID:33864376	PCS	HP:0003577	1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0007651	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001537	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000403	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000527	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0007874	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0001511	PMID:33864376	PCS	HP:0011461	2/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0200055	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000322	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000006	PMID:33864376	PCS					I	HPO:probinson[2021-10-02];HPO:probinson[2021-10-02]
OMIM:619460	Luo-Schoch-Yamamoto syndrome		HP:0000445	PMID:33864376	PCS		1/2			P	HPO:probinson[2021-10-02]
OMIM:600131	Epilepsy, childhood absence, susceptibility to, 1		HP:0002069	OMIM:600131	TAS					P	HPO:iea[2009-02-17]
OMIM:600131	Epilepsy, childhood absence, susceptibility to, 1		HP:0010849	OMIM:600131	TAS					P	HPO:iea[2009-02-17]
OMIM:600131	Epilepsy, childhood absence, susceptibility to, 1		HP:0002373	OMIM:600131	TAS					P	HPO:iea[2009-02-17]
OMIM:600131	Epilepsy, childhood absence, susceptibility to, 1		HP:0002121	OMIM:600131	TAS					P	HPO:iea[2009-02-17]
OMIM:600131	Epilepsy, childhood absence, susceptibility to, 1		HP:0011463	OMIM:600131	TAS					C	HPO:iea[2012-07-20]
OMIM:600131	Epilepsy, childhood absence, susceptibility to, 1		HP:0002392	OMIM:600131	TAS					P	HPO:iea[2012-07-20]
OMIM:600131	Epilepsy, childhood absence, susceptibility to, 1		HP:0000006	OMIM:600131	TAS					I	HPO:iea[2009-02-17]
OMIM:273300	Testicular tumor, somatic		HP:0001442	OMIM:273300	TAS					I	HPO:skoehler[2015-12-30]
OMIM:273300	Testicular tumor, somatic		HP:0009792	OMIM:273300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:273300	Testicular tumor, somatic		HP:0100768	OMIM:273300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:273300	Testicular tumor, somatic		HP:0006254	OMIM:273300	TAS					P	HPO:probinson[2020-07-14]
OMIM:273300	Testicular tumor, somatic		HP:0003745	OMIM:273300	IEA					I	HPO:iea[2009-02-17]
OMIM:273300	Testicular tumor, somatic		HP:0002898	OMIM:273300	TAS					P	HPO:probinson[2020-07-14]
OMIM:273300	Testicular tumor, somatic		HP:0000027	OMIM:273300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607676	Immunodeficiency 67		HP:0001287	PMID:16950813	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0410255	PMID:12637671	PCS				HP:0025215	P	HPO:probinson[2020-07-25]
OMIM:607676	Immunodeficiency 67		HP:0003212	PMID:12637671	PCS		2/3			P	HPO:probinson[2020-07-25]
OMIM:607676	Immunodeficiency 67		HP:0410300	PMID:16950813	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0020096	PMID:12637671	PCS		3/3			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:607676	Immunodeficiency 67		HP:0011839	PMID:16950813	PCS		0/1			P	HPO:probinson[2020-07-25];HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0003593	PMID:12637671	PCS		3/3			C	HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0003095	PMID:16950813	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0010975	PMID:16950813	PCS		0/1			P	HPO:probinson[2020-07-25];HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0100523	PMID:12637671	PCS		1/3			P	HPO:probinson[2020-07-25]
OMIM:607676	Immunodeficiency 67		HP:0011463	PMID:16950813	PCS		1/1			C	HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0040089	PMID:16950813	PCS		0/1			P	HPO:probinson[2020-07-25];HPO:probinson[2024-03-13]
OMIM:607676	Immunodeficiency 67		HP:0000007	PMID:12637671	PCS					I	HPO:probinson[2020-07-25]
OMIM:607676	Immunodeficiency 67		HP:0007499	PMID:12637671	PCS		3/3			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:607676	Immunodeficiency 67		HP:0002721	OMIM:607676	IEA					P	HPO:skoehler[2015-01-27]
OMIM:608545	Larsen-Like syndrome		HP:0004322	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000260	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0001252	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0001373	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0001290	OMIM:608545	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608545	Larsen-Like syndrome		HP:0012368	OMIM:608545	TAS					P	HPO:skoehler[2013-10-22]
OMIM:608545	Larsen-Like syndrome		HP:0011220	OMIM:608545	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608545	Larsen-Like syndrome		HP:0000316	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0003745	OMIM:608545	IEA					I	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000256	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0002751	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000175	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0001762	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0002750	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0001382	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0001263	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000272	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0005285	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000403	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000689	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0009279	OMIM:608545	TAS					P	HPO:probinson[2012-05-01]
OMIM:608545	Larsen-Like syndrome		HP:0008127	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000405	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0004209	OMIM:608545	TAS					P	HPO:probinson[2012-05-01]
OMIM:608545	Larsen-Like syndrome		HP:0002007	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000248	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:608545	Larsen-Like syndrome		HP:0000369	OMIM:608545	IEA					P	HPO:iea[2009-02-17]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000286	PMID:19764020	PCS		0/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0003577	PMID:19764020	PCS		4/4			C	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001355	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001250	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0002000	PMID:19764020	PCS		3/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000262	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0003196	PMID:19764020	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0010669	PMID:19764020	PCS		3/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0012444	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0008551	PMID:19764020	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000717	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000238	PMID:19764020	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0002119	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000256	PMID:19764020	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0002019	PMID:19764020	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001249	PMID:19764020	PCS		4/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0002058	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001561	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000494	PMID:19764020	PCS		1/4			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000252	PMID:19764020	PCS		0/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000431	PMID:19764020	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001762	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000750	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000276	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000034	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001263	PMID:19764020	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0002251	PMID:19764020	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0045025	PMID:19764020	PCS		3/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001182	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0030746	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000308	PMID:19764020	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000729	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000508	PMID:19764020	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000348	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001357	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0002007	PMID:19764020	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000322	PMID:19764020	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000960	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000303	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000369	PMID:19764020	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000006	PMID:19764020	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0001611	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:613603	Chromosome 4q32.1-q32.2 triplication syndrome		HP:0000544	PMID:19764020	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0000252	PMID:23623386	PCS		1/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0003577	PMID:23623386	PCS		2/2			C	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0004322	PMID:23623386	PCS		2/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0002032	PMID:23623386	PCS		1/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0010445	PMID:23623386	PCS		1/2			P	HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0040012	PMID:23623386	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0000007	PMID:23623386	PCS					I	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0009777	PMID:23623386	PCS		1/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0005528	PMID:23623386	PCS		2/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0005912	PMID:23623386	PCS		1/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0001510	PMID:23623386	PCS		2/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0000369	PMID:23623386	PCS		1/2			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-03-15]
OMIM:615272	Fanconi anemia, complementation group Q		HP:0001545	PMID:23623386	PCS		1/2			P	HPO:probinson[2022-03-15]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0000164	OMIM:221320	TAS					P	HPO:probinson[2013-03-24]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0000968	OMIM:221320	IEA					P	HPO:iea[2009-02-17]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0000508	OMIM:221320	IEA					P	HPO:iea[2009-02-17]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0000007	OMIM:221320	IEA					I	HPO:iea[2009-02-17]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0000405	OMIM:221320	IEA					P	HPO:skoehler[2010-06-18]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0004209	OMIM:221320	IEA					P	HPO:iea[2009-02-17]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0000389	OMIM:221320	IEA					P	HPO:iea[2009-02-17]
OMIM:221320	Deafness, conductive, with ptosis and skeletal anomalies		HP:0000413	OMIM:221320	IEA					P	HPO:iea[2009-02-17]
OMIM:602068	Leishmaniasis, tegumentary		HP:0007408	OMIM:602068	IEA					P	HPO:iea[2009-02-17]
OMIM:602068	Leishmaniasis, tegumentary		HP:0000007	OMIM:602068	IEA					I	HPO:iea[2009-02-17]
OMIM:602068	Leishmaniasis, tegumentary		HP:0003831	OMIM:602068	IEA					I	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001650	PMID:15368195	PCS		2/6			P	HPO:skoehler[2010-06-18];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000189	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001156	PMID:15368195	PCS		6/6			P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0004322	PMID:15368195	PCS		6/6			P	HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0002682	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001230	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001072	OMIM:277600	IEA					P	HPO:skoehler[2019-04-18]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001629	OMIM:277600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000518	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0002938	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000618	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0003508	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001643	OMIM:277600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0009768	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001642	PMID:15368195	PCS		2/6			P	HPO:skoehler[2010-06-18];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001169	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0002753	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000594	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000692	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0002650	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0030961	PMID:15368195	PCS		6/6			P	HPO:skoehler[2017-07-13];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001387	PMID:15368195	PCS		6/6			P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001783	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001083	PMID:15368195	PCS		6/6			P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0011003	PMID:15368195	PCS		6/6			P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0005280	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0006482	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000327	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000007	PMID:15368195	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0003416	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000586	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0001653	OMIM:277600	IEA					P	HPO:skoehler[2010-06-18]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000501	PMID:15368195	PCS		6/6			P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000248	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:277600	Weill-Marchesani syndrome 1		HP:0000885	OMIM:277600	IEA					P	HPO:iea[2009-02-17]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000286	PMID:28013294	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002540	PMID:28013294	PCS		10/13			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002188	PMID:28013294	PCS		3/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000123	PMID:28013294	PCS		4/13			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001371	PMID:28013294;PMID:31070736	PCS		18/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0008807	OMIM:617303	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001252	PMID:31070736	PCS		5/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0003593	PMID:27547915	PCS		2/2			C	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0003073	PMID:31070736	PCS		5/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000280	PMID:28013294;PMID:27547915;PMID:31070736	PCS		19/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000639	PMID:31070736	PCS		1/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0011220	PMID:28013294	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0012471	OMIM:617303	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0100806	PMID:31070736	PCS		1/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0005528	PMID:28013294	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000158	PMID:28013294;PMID:27547915	PCS		11/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001643	PMID:28013294;PMID:31070736	PCS		8/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001007	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001403	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001265	PMID:31070736	PCS		3/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000252	PMID:27547915	PCS		1/2			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0006538	PMID:31070736	PCS		5/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001344	PMID:28013294	PCS		13/13			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000097	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001263	PMID:28013294;PMID:27547915	PCS		15/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000294	PMID:27547915	PCS		1/2			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000093	PMID:28013294;PMID:27547915;PMID:31070736	PCS		20/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000092	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0040030	PMID:31070736	PCS		1/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002869	PMID:28013294	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000767	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000007	PMID:28013294	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001217	PMID:27547915	PCS		1/2			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000527	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000648	PMID:28013294	PCS		6/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000768	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000445	PMID:28013294	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002003	PMID:27547915	PCS		1/2			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0003016	PMID:28013294	PCS					P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000100	PMID:31070736	PCS		4/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0003496	PMID:31070736	PCS		4/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002162	PMID:27547915	PCS		1/2			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002240	PMID:28013294;PMID:27547915	PCS		14/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002680	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001072	PMID:28013294	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001270	PMID:31070736	PCS		5/5			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0012444	PMID:28013294	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001903	PMID:28013294;PMID:27547915;PMID:31070736	PCS		20/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0006532	PMID:27547915	PCS		2/2			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002514	PMID:28013294	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001744	PMID:28013294;PMID:27547915;PMID:31070736	PCS		19/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000431	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001882	PMID:28013294	PCS		8/13			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002098	PMID:28013294;PMID:27547915	PCS		15/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000470	PMID:28013294;PMID:27547915	PCS		14/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0003819	PMID:28013294	PCS		11/13			C	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001639	PMID:28013294	PCS		9/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000506	PMID:28013294	PCS		13/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000943	PMID:28013294;PMID:27547915;PMID:31070736	PCS		20/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001635	PMID:28013294	PCS		11/13			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002208	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0002205	PMID:28013294;PMID:31070736	PCS		18/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000664	PMID:27547915	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001873	PMID:28013294;PMID:31070736	PCS		16/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001631	PMID:28013294	PCS		7/13			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0000105	PMID:28013294	PCS		3/13			P	HPO:probinson[2021-02-19]
OMIM:617303	Mucopolysaccharidosis-Plus syndrome		HP:0001875	PMID:31070736	PCS		4/5			P	HPO:probinson[2021-02-19]
OMIM:109400	Basal cell nevus syndrome		HP:0001056	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0000242	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0000486	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0010609	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0000283	OMIM:109400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:109400	Basal cell nevus syndrome		HP:0000280	PMID:9096761	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0010442	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0010603	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0003621				P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0004280	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0000518	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0002937	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0000316	PMID:9096761	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0000238	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0000912	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0002414	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0200021	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0005449	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0001249	OMIM:109400	IEA		HP:0040283			P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0001144	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0002751	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0000175	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0000892	PMID:9096761	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0009729	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0002671	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0011462				P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0005462	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0011462				P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0009650	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0010044	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0002948	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0000568	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0009730	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0000766	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0005815	OMIM:109400	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0000006	OMIM:109400	PCS					I	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0000204	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0001156	OMIM:109400	TAS					P	HPO:skoehler[2014-11-26]
OMIM:109400	Basal cell nevus syndrome		HP:0001270	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0000612	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0000256	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0003577				P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0000773	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0025318	OMIM:109400	TAS					P	HPO:skoehler[2017-07-13]
OMIM:109400	Basal cell nevus syndrome		HP:0010618	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0010617	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0002650	OMIM:109400	PCS					P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0000431	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0004795	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:109400	Basal cell nevus syndrome		HP:0010610	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0010612	PMID:9096761	PCS					P	HPO:iea[2009-10-28]
OMIM:109400	Basal cell nevus syndrome		HP:0008422	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS					P	HPO:iea[2009-10-27]
OMIM:109400	Basal cell nevus syndrome		HP:0002007	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns;OMIM:109400	PCS		20/20			P	HPO:skoehler[2012-10-12];HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0002885	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0011463				P	HPO:iea[2009-02-17]
OMIM:109400	Basal cell nevus syndrome		HP:0000303	PMID:12116218	PCS				HP:0012825	P	HPO:probinson[2012-04-30]
OMIM:109400	Basal cell nevus syndrome		HP:0000501	OMIM:109400	IEA					P	HPO:skoehler[2012-10-12]
OMIM:610478	Retinal cone dystrophy 4		HP:0001133	OMIM:610478	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610478	Retinal cone dystrophy 4		HP:0007814	PMID:17033974	PCS					P	HPO:probinson[2017-06-16]
OMIM:610478	Retinal cone dystrophy 4		HP:0000613	OMIM:610478	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610478	Retinal cone dystrophy 4		HP:0000007	PMID:17033974	PCS					I	HPO:probinson[2013-01-09]
OMIM:610478	Retinal cone dystrophy 4		HP:0007663	OMIM:610478	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610478	Retinal cone dystrophy 4		HP:0000505	PMID:17033974	PCS				HP:0012825	P	HPO:probinson[2013-02-28]
OMIM:610478	Retinal cone dystrophy 4		HP:0007984	PMID:17033974	PCS					P	HPO:probinson[2013-02-28]
OMIM:610478	Retinal cone dystrophy 4		HP:0000548	PMID:17033974	PCS					P	HPO:skoehler[2015-12-30]
OMIM:609129	Auditory neuropathy, autosomal dominant, 1		HP:0008529	PMID:15675004	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:609129	Auditory neuropathy, autosomal dominant, 1		HP:0003621	PMID:15675004	PCS					C	HPO:probinson[2022-03-13]
OMIM:609129	Auditory neuropathy, autosomal dominant, 1		HP:0006958	PMID:15675004	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:609129	Auditory neuropathy, autosomal dominant, 1		HP:0000407	PMID:15675004	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:609129	Auditory neuropathy, autosomal dominant, 1		HP:0011462	PMID:15675004	PCS					C	HPO:probinson[2022-03-13]
OMIM:609129	Auditory neuropathy, autosomal dominant, 1		HP:0000006	PMID:15675004	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:609129	Auditory neuropathy, autosomal dominant, 1		HP:0001963	PMID:15675004	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0001696	PMID:24094744	PCS	HP:0003577	3/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0002110	PMID:24094744	PCS		2/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0033036	PMID:24094744	PCS		4/4			P	HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0012207	OMIM:615500	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0011108	PMID:24094744	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0200073	OMIM:615500	TAS					P	HPO:skoehler[2013-11-18]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0012265	PMID:24094744	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0012256	PMID:24094744	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0012384	OMIM:615500	TAS				HP:0031796	P	HPO:skoehler[2013-11-18]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0012263	PMID:24094744	IEA		1/1			P	HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0000789	OMIM:615500	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0000007	PMID:24094744	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0000403	PMID:24094744	PCS		3/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0002205	PMID:24094744	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0002643	PMID:24094744	PCS	HP:0003623	4/4			P	HPO:probinson[2020-09-13]
OMIM:615500	Ciliary dyskinesia, primary, 26		HP:0004469	PMID:24094744	PCS					P	HPO:skoehler[2013-11-18];HPO:probinson[2020-09-13]
OMIM:613617	Retinitis pigmentosa 58		HP:0007737	PMID:20797688	PCS					P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0003621	PMID:20797688	PCS		4/4			C	HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0000662	PMID:20797688	PCS	HP:0003621	4/4			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0000608	PMID:20797688	PCS		4/4			P	HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0001141	PMID:20797688	PCS		4/4			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0008323	PMID:20797688	PCS		4/4			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0000007	PMID:20797688	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0007994	PMID:20797688	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0000543	PMID:20797688	PCS		4/4			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0000510	PMID:20797688	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-09-25]
OMIM:613617	Retinitis pigmentosa 58		HP:0007843	PMID:20797688	PCS		4/4			P	HPO:probinson[2013-06-02];HPO:probinson[2022-09-25]
OMIM:189200	Toes, relative length of first and second		HP:0000924	OMIM:189200	IEA					P	HPO:iea[2009-02-17]
OMIM:189200	Toes, relative length of first and second		HP:0000006	OMIM:189200	IEA					I	HPO:iea[2009-02-17]
OMIM:615266	Hypogonadotropic hypogonadism 17 with or without anosmia		HP:0000044	PMID:23643382	PCS					P	HPO:probinson[2022-10-22]
OMIM:615266	Hypogonadotropic hypogonadism 17 with or without anosmia		HP:0000164	PMID:23643382	PCS		2/14			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-10-22]
OMIM:615266	Hypogonadotropic hypogonadism 17 with or without anosmia		HP:0000365	PMID:23643382	PCS		3/14			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-10-22]
OMIM:615266	Hypogonadotropic hypogonadism 17 with or without anosmia		HP:0000938	PMID:23643382	PCS		2/14			P	HPO:probinson[2022-10-22]
OMIM:615266	Hypogonadotropic hypogonadism 17 with or without anosmia		HP:0004409	PMID:23643382	PCS					P	HPO:probinson[2022-10-22]
OMIM:615266	Hypogonadotropic hypogonadism 17 with or without anosmia		HP:0000006	PMID:23643382	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-22]
OMIM:140000	Hand-foot-uterus syndrome		HP:0001792	PMID:9020844	PCS					P	HPO:probinson[2023-03-04]
OMIM:140000	Hand-foot-uterus syndrome		HP:0010109	PMID:9020844	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:140000	Hand-foot-uterus syndrome		HP:0001156	OMIM:140000	TAS					P	HPO:skoehler[2015-12-30]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000083	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000041	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0010105	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0012330	OMIM:140000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:140000	Hand-foot-uterus syndrome		HP:0010034	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0009464	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0006110	OMIM:140000	TAS					P	HPO:probinson[2012-06-09]
OMIM:140000	Hand-foot-uterus syndrome		HP:0009623	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0001885	OMIM:140000	TAS					P	HPO:probinson[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000076	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000054	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0001245	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0003762	PMID:9020844	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000074	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0008080	PMID:9020844	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:140000	Hand-foot-uterus syndrome		HP:0010584	OMIM:140000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:140000	Hand-foot-uterus syndrome		HP:0008103	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0008740	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0009237	OMIM:140000	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0004209	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000048	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000047	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0001216	OMIM:140000	IEA					P	HPO:iea[2009-02-17]
OMIM:140000	Hand-foot-uterus syndrome		HP:0000006	PMID:9020844	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-04]
OMIM:187510	Tetramelic monodactyly		HP:0004058	OMIM:187510	TAS					P	HPO:probinson[2009-02-17]
OMIM:187510	Tetramelic monodactyly		HP:0001839	OMIM:187510	TAS					P	HPO:probinson[2013-03-11]
OMIM:187510	Tetramelic monodactyly		HP:0001171	OMIM:187510	TAS					P	HPO:probinson[2009-02-17]
OMIM:187510	Tetramelic monodactyly		HP:0200054	OMIM:187510	TAS					P	HPO:probinson[2013-03-11]
OMIM:187510	Tetramelic monodactyly		HP:0000006	OMIM:187510	TAS					I	HPO:probinson[2009-02-17]
OMIM:619361	Angioedema, hereditary, 5		HP:0100665	PMID:28601681	PCS	HP:0003621	4/4			P	HPO:probinson[2021-07-13]
OMIM:619361	Angioedema, hereditary, 5		HP:0033250	PMID:28601681	PCS					P	HPO:probinson[2021-07-13]
OMIM:619361	Angioedema, hereditary, 5		HP:0000282	PMID:28601681	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619361	Angioedema, hereditary, 5		HP:0030254	PMID:28601681	PCS					P	HPO:probinson[2021-07-13]
OMIM:619361	Angioedema, hereditary, 5		HP:0031244	PMID:28601681	PCS				HP:0031796	P	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:619361	Angioedema, hereditary, 5		HP:0000006	PMID:28601681	PCS					I	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:619361	Angioedema, hereditary, 5		HP:0007514	PMID:28601681	PCS				HP:0031796	P	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:151630	Lip, median nodule of upper		HP:0000153	OMIM:151630	IEA					P	HPO:iea[2009-02-17]
OMIM:151630	Lip, median nodule of upper		HP:0000006	OMIM:151630	IEA					I	HPO:iea[2009-02-17]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0003236	PMID:23390185	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0030046	PMID:23390185	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0003691	PMID:23390185	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0011463	PMID:23390185	PCS		4/4			C	HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0007340	PMID:23390185	PCS		4/4			P	HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0008981	PMID:23390185	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0032341	PMID:23390185	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0000007	PMID:23390185	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0006785	PMID:23390185	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0002505	PMID:23390185	PCS	HP:0025710	3/4			P	HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0000158	PMID:23390185	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0001324	PMID:23390185	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-20]
OMIM:616052	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7		HP:0003677	PMID:23390185	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0000819	OMIM:222100	IEA					P	HPO:iea[2009-02-17]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0002960	OMIM:222100	TAS					P	HPO:skoehler[2018-10-08]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0001993	OMIM:222100	IEA					P	HPO:iea[2009-02-17]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0001959	OMIM:222100	IEA					P	HPO:iea[2009-02-17]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0002591	OMIM:222100	IEA					P	HPO:iea[2009-02-17]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0003074	OMIM:222100	IEA					P	HPO:iea[2009-02-17]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0410050	PMID:9357814;PMID:17659063;PMID:16731998	PCS		30/30			P	HPO:NicoleVasilevsky[2018-02-23];HPO:NicoleVasilevsky[2018-03-02]
OMIM:222100	Diabetes mellitus, insulin-dependent-1		HP:0000103	OMIM:222100	IEA					P	HPO:iea[2009-02-17]
OMIM:600630	UV-sensitive syndrome 1		HP:0003224	PMID:22466610	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0002664	OMIM:600630	IEA					P	HPO:iea[2009-02-17]
OMIM:600630	UV-sensitive syndrome 1		HP:0000992	PMID:15486090;PMID:22466610	PCS		2/2			P	HPO:probinson[2022-04-10];HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0000958	PMID:15486090	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0001480	PMID:15486090	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0000707	PMID:15486090	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0003593	PMID:22466610	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0001009	PMID:15486090	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0000007	PMID:15486090	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-10]
OMIM:600630	UV-sensitive syndrome 1		HP:0007623	PMID:15486090	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:600156	Hirschsprung disease, susceptibility to, 5		HP:0002251	OMIM:600156	IEA					P	HPO:iea[2009-02-17]
OMIM:600156	Hirschsprung disease, susceptibility to, 5		HP:0000006	OMIM:600156	TAS					I	HPO:skoehler[2012-10-17]
OMIM:618719	Megabladder, congenital		HP:0003774	PMID:31513549	PCS		1/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0100611	PMID:31513549	PCS		1/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0010956	PMID:31513549	PCS	HP:0011461	13/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0001629	PMID:31513549	PCS		2/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0004719	PMID:31513549	PCS		2/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0001647	PMID:31513549	PCS		1/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0011664	PMID:31513549	PCS		1/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0001643	PMID:31513549	PCS		1/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0001631	PMID:31513549	PCS		1/14			P	HPO:probinson[2020-07-22]
OMIM:618719	Megabladder, congenital		HP:0000006	PMID:31513549	TAS					I	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0003202	PMID:30918256	PCS		13/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0003687	PMID:30918256	PCS		12/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0002015	PMID:30918256	PCS		10/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0003236	PMID:30918256	PCS		14/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0003581	PMID:30918256	PCS		14/14			C	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0034722	PMID:30918256;PMID:35527200;PMID:16146490	PCS		21/24			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18];HPO:probinson[2023-07-18];HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0030319	PMID:30918256	PCS		0/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0009005	PMID:30918256	PCS		13/14			P	HPO:probinson[2023-07-03];HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0003803	PMID:30918256	PCS		8/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0002747	PMID:30918256	PCS		9/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0003327	PMID:30918256	PCS		13/14			P	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0000006	PMID:30918256	PCS					I	HPO:probinson[2023-07-03]
OMIM:620286	Myopathy, sarcoplasmic body		HP:0003557	PMID:30918256	PCS		11/14			P	HPO:probinson[2023-07-03]
OMIM:619407	WHIM syndrome 2		HP:0031160	PMID:34854278;PMID:24777453	PCS		3/6			P	HPO:probinson[2021-08-20];HPO:probinson[2022-05-16]
OMIM:619407	WHIM syndrome 2		HP:0034284	PMID:34854278	PCS		4/4			P	HPO:probinson[2022-06-04]
OMIM:619407	WHIM syndrome 2		HP:0011463	PMID:34854278	PCS		4/4			C	HPO:probinson[2022-05-16]
OMIM:619407	WHIM syndrome 2		HP:0410252	PMID:34854278;PMID:24777453	PCS		6/6			P	HPO:probinson[2021-08-20];HPO:probinson[2022-05-16]
OMIM:619407	WHIM syndrome 2		HP:0001636	PMID:34854278	PCS		0/4			P	HPO:probinson[2022-05-16]
OMIM:619407	WHIM syndrome 2		HP:0000007	PMID:24777453	PCS					I	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:619407	WHIM syndrome 2		HP:0032169	PMID:34854278	PCS		2/4			P	HPO:probinson[2022-05-16]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000286	PMID:26637975	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000046	PMID:26637975	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000486	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0004322	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0001250	PMID:26637975	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000160	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0001252	OMIM:616734	TAS				HP:0012825	P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000482	OMIM:616734	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0001290	OMIM:616734	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0012745	PMID:26637975	PCS		3/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000316	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0100807	OMIM:616734	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0001763	OMIM:616734	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0001249	PMID:26637975	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000358	PMID:26637975	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000175	PMID:26637975	PCS		3/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000494	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000252	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0002079	PMID:26637975	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000691	OMIM:616734	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000294	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0004691	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0001182	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000767	OMIM:616734	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000568	PMID:26637975	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0004209	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000047	PMID:26637975	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000006	PMID:26637975	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000369	PMID:26637975	PCS		3/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000582	PMID:26637975	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0003577	PMID:26637975	PCS		4/4			C	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000581	OMIM:616734	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0001270	OMIM:616734	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0012368	PMID:26637975	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0008551	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000219	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0002119	PMID:26637975	PCS		2/2		HP:0012825	P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0006610	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000396	PMID:26637975	PCS		2/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000670	OMIM:616734	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000475	OMIM:616734	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000750	OMIM:616734	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0004279	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000431	PMID:26637975	PCS		4/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000276	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000470	PMID:26637975	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0009909	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0034400	PMID:26637975	PCS		4/4			P	HPO:probinson[2022-12-18]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000070	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0005280	PMID:26637975	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000508	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000664	PMID:26637975	PCS		1/4			P	HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000028	PMID:26637975	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:616734	Skin creases, congenital symmetric circumferential, 2		HP:0000347	OMIM:616734	TAS					P	HPO:skoehler[2015-12-30]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0002242	OMIM:251850	TAS					P	HPO:probinson[2009-02-17]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0004385	PMID:18724368	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-23]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0011473	OMIM:251850	TAS					P	HPO:probinson[2013-12-21]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0004395	OMIM:251850	TAS					P	HPO:probinson[2009-02-17]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0001944	OMIM:251850	TAS					P	HPO:probinson[2009-02-17]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0000007	OMIM:251850	TAS					I	HPO:probinson[2009-02-17]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0001522	OMIM:251850	TAS					C	HPO:probinson[2009-02-17]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0001510	OMIM:251850	TAS					P	HPO:probinson[2009-02-17]
OMIM:251850	Diarrhea 2, with microvillous atrophy		HP:0003623	PMID:18724368	PCS		11/11			C	HPO:probinson[2022-06-23]
OMIM:226400	Epidermodysplasia verruciformis, susceptibility to, 1		HP:0002671	OMIM:226400	IEA					P	HPO:iea[2009-02-17]
OMIM:226400	Epidermodysplasia verruciformis, susceptibility to, 1		HP:0001939	OMIM:226400	IEA					P	HPO:iea[2009-02-17]
OMIM:226400	Epidermodysplasia verruciformis, susceptibility to, 1		HP:0000007	OMIM:226400	IEA					I	HPO:skoehler[2019-04-18]
OMIM:226400	Epidermodysplasia verruciformis, susceptibility to, 1		HP:0200043	OMIM:226400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001410	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000046	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0004322	PMID:19161147	PCS		8/8			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001250	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001252	PMID:29979980	PCS		5/5			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002020	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0003593	OMIM:613658	IEA					C	HPO:skoehler[2019-04-18]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001290	OMIM:613658	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0003073	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001409	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001408	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0011220	PMID:29979980	PCS		2/5			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0011461	PMID:29573043	PCS		1/1			C	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001328	PMID:19161147	PCS		7/7			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0003546	PMID:19161147	PCS		8/8			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000252	PMID:19161147	PCS		8/8			P	HPO:skoehler[2012-10-17];HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000010	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001541	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002750	PMID:19161147	PCS		7/7			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0011968	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001382	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000490	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001263	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0012735	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0008282	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000767	PMID:29979980	PCS		2/5			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002748	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000007	PMID:29979980	PCS					I	HPO:skoehler[2012-10-17];HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000601	PMID:29979980	PCS		2/5			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002901	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001533	OMIM:613658	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002789	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001397	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001396	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000023	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001394	PMID:29979980;PMID:29573043	PCS		3/6			P	HP:probinson[2019-02-19];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002040	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001508	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001903	PMID:19161147	PCS		7/7			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000938	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0006530	PMID:29979980;PMID:29573043	PCS		6/6			P	HP:probinson[2019-02-19];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001943	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002878	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0012050	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0000218	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002315	PMID:19161147	PCS		7/7			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002514	PMID:29979980;PMID:19161147	PCS		11/12			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002910	PMID:29979980;PMID:29573043	PCS		3/6			P	HP:probinson[2019-02-19];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002753	PMID:19161147	PCS		7/7			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0008936	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001562	PMID:29573043	PCS	HP:0011461	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002059	OMIM:613658	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002650	PMID:29979980	PCS		2/5			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002013	PMID:29573043	PCS	HP:0003593	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002097	OMIM:613658	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002093	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0032988	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0100512	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001518	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0004905	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001511	PMID:29573043	PCS		1/1			P	HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0004944	PMID:29979980	PCS		2/2			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001510	PMID:19161147	PCS		8/8			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0002566	PMID:29979980	PCS		2/5			P	HP:probinson[2019-02-19]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0001876	PMID:29573043	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-25]
OMIM:613658	Rajab interstitial lung disease with brain calcifications		HP:0004349	PMID:29979980	PCS		2/5			P	HP:probinson[2019-02-19]
OMIM:115700	Cataract, crystalline aculeiform		HP:0000519	OMIM:115700	IEA					P	HPO:iea[2009-02-17]
OMIM:115700	Cataract, crystalline aculeiform		HP:0000006	OMIM:115700	IEA					I	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001297	PMID:34946904;PMID:19387015	PCS		3/7			P	HPO:probinson[2022-05-29];HPO:skoehler[2018-10-08];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0003596	PMID:34946904	PCS		1/1			C	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002200	PMID:19387015	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001310	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001596	PMID:19387015	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0000020	PMID:34946904	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002063	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001251	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0010521	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002381	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0012444	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0100546	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0007162	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0000639	OMIM:600142	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0000738	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0000739	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0007204	PMID:19387015	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001347	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0004931	PMID:19387015	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0003621	PMID:19387015	PCS		5/6			C	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001288	PMID:19387015	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0003487	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002352	PMID:34946904	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001260	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002071	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0032325	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0025708	PMID:19387015	PCS		1/6			C	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0000726	PMID:34946904;PMID:19387015	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002607	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0003419	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0000007	PMID:19387015	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0007256	PMID:19387015	PCS		6/6			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0000746	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002326	PMID:34946904	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0001257	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:600142	Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)		HP:0002448	OMIM:600142	IEA					P	HPO:iea[2009-02-17]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000286	PMID:27620904	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0002069	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0002342	PMID:30213762;PMID:25356899	PCS		2/2			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0031627	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000486	PMID:34930816	PCS		4/26			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0001250	PMID:25356899;PMID:34930816	PCS		14/29			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0002384	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0001252	PMID:30213762;PMID:27620904;PMID:34930816	PCS		15/20			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0002360	PMID:27620904;PMID:34930816	PCS		18/23			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0003196	PMID:34930816	PCS					P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0003593	PMID:30213762	PCS		1/1			C	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0002020	PMID:34930816	PCS		3/23			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0001270	PMID:34930816	PCS		28/30			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000718	PMID:34930816	PCS		11/24			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000739	PMID:34930816	PCS		7/8			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000733	PMID:27620904	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000414	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000219	PMID:34930816	PCS					P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000752	PMID:27620904	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000311	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0001249	PMID:27620904	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0003502	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000494	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000750	PMID:25356899;PMID:27620904;PMID:34930816	PCS		32/32			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0002133	PMID:25356899	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000431	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0031936	PMID:25356899	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0002373	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0011968	PMID:34930816	PCS		10/23			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0001263	PMID:30213762;PMID:23020937;PMID:27620904;PMID:34930816	PCS		34/34			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000506	PMID:30213762	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000729	PMID:34930816	PCS		24/30			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000348	PMID:34930816	PCS					P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0007874	PMID:34930816	PCS					P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000400	PMID:27620904	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0007018	PMID:34930816	PCS		15/22			P	HPO:probinson[2023-06-24]
OMIM:620292	Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures		HP:0000006	PMID:23020937	PCS					I	HPO:probinson[2023-06-24]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0001760	OMIM:158600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0003445	OMIM:158600	TAS					P	HPO:probinson[2009-02-17]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0011808	OMIM:158600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0031936	OMIM:158600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0003474	OMIM:158600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0001263	OMIM:158600	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0010602	OMIM:158600	TAS					P	HPO:probinson[2012-04-27]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0011463	OMIM:158600	TAS					C	HPO:probinson[2012-04-27]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0009046	OMIM:158600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0002515	OMIM:158600	TAS					P	HPO:probinson[2012-04-27]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0007269	OMIM:158600	TAS					P	HPO:probinson[2009-02-17]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0000006	OMIM:158600	TAS					I	HPO:probinson[2012-04-27]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0008956	OMIM:158600	TAS					P	HPO:probinson[2012-04-27]
OMIM:158600	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant		HP:0003677	OMIM:158600	TAS					C	HPO:skoehler[2012-11-21]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0002421	PMID:26626625	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0003577	PMID:26626625	PCS		3/3			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0010628	PMID:26626625	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0001552	PMID:26626625	PCS		1/3			P	HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0002783	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0020152	PMID:26626625	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0001252	PMID:26626625	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0002460	PMID:26626625	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0002020	PMID:26626625	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0001290	PMID:26626625	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0001270	PMID:26626625	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0000218	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0003327	PMID:26626625	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0003701	PMID:26626625	PCS		2/3			P	HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0000278	PMID:26626625	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0003306	PMID:26626625	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0003403	PMID:26626625	PCS		2/2			P	HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0003546	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0030205	PMID:26626625	PCS		2/2			P	HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0001761	PMID:26626625	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0001283	PMID:26626625	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0011968	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0002093	PMID:26626625	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0000508	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0000007	PMID:26626625	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0000768	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0000369	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0000347	PMID:26626625	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616720	Myasthenic syndrome, congenital, 19		HP:0003557	PMID:26626625	PCS		1/3			P	HPO:probinson[2023-02-04]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0000099	PMID:33087723	PCS		2/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0003621	PMID:33087723	PCS		3/10			C	HPO:probinson[2021-07-12];HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0003596	PMID:33087723	PCS		1/10			C	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0030388	PMID:33087723	PCS		7/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0020151	PMID:33087723	PCS		3/9			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0003493	PMID:33087723	PCS		5/9			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0002240	PMID:33087723	PCS		1/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0033631	PMID:33087723	PCS		1/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0033028	PMID:33087723	PCS		5/9			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0012189	PMID:33087723	PCS		1/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0011463	PMID:33087723	PCS		4/10			C	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0011462	PMID:33087723	PCS		2/10			C	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0100646	PMID:33087723	PCS		1/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0002608	PMID:33087723	PCS		1/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0030384	PMID:33087723	PCS		7/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0002716	PMID:33087723	PCS		2/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0002725	PMID:33087723	PCS		2/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0001973	PMID:33087723	PCS		3/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0002205	PMID:33087723	PCS		1/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0000006	PMID:33087723	PCS					I	HPO:probinson[2021-07-12];HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0001744	PMID:33087723	PCS		2/10			P	HPO:probinson[2021-07-12]
OMIM:619375	Autoinflammatory syndrome, familial, with or without immunodeficiency		HP:0004844	PMID:33087723	PCS		3/9			P	HPO:probinson[2021-07-12]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000176	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0001760	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000384	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0004467	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000211	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000486	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0004322	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0004452	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000407	OMIM:609166	TAS					P	HPO:skoehler[2014-05-04]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0009795	OMIM:609166	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0009882	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0009796	OMIM:609166	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000410	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000006	OMIM:609166	IEA					I	HPO:iea[2009-02-17]
OMIM:609166	Branchiogenic-deafness syndrome		HP:0000413	OMIM:609166	IEA					P	HPO:iea[2009-02-17]
OMIM:600624	Cone-Rod dystrophy 1		HP:0003621	OMIM:600624	IEA					C	HPO:iea[2009-02-17]
OMIM:600624	Cone-Rod dystrophy 1		HP:0000365	OMIM:600624	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600624	Cone-Rod dystrophy 1		HP:0011463	OMIM:600624	TAS					C	HPO:skoehler[2012-10-17]
OMIM:600624	Cone-Rod dystrophy 1		HP:0000548	OMIM:600624	IEA					P	HPO:iea[2009-02-17]
OMIM:600624	Cone-Rod dystrophy 1		HP:0000598	OMIM:600624	IEA					P	HPO:iea[2009-02-17]
OMIM:600624	Cone-Rod dystrophy 1		HP:0000135	OMIM:600624	IEA					P	HPO:iea[2009-02-17]
OMIM:600624	Cone-Rod dystrophy 1		HP:0000006	OMIM:600624	IEA					I	HPO:iea[2009-02-17]
OMIM:600624	Cone-Rod dystrophy 1		HP:0001249	OMIM:600624	IEA					P	HPO:iea[2009-02-17]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0000365	PMID:17332895	PCS		2/2			P	HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0002151	PMID:17332895	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0001284	PMID:17332895	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0002092	PMID:17332895	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0032653	PMID:17332895	PCS		2/2			P	HPO:probinson[2022-12-20];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0033505	PMID:17332895	PCS		2/2			P	HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0011463	PMID:17332895	PCS		2/2			C	HPO:probinson[2022-12-20];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0009830	PMID:17332895	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0000007	PMID:17332895	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0025502	PMID:17332895	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0000648	PMID:17332895	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0100739	PMID:17332895	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0001659	PMID:17332895	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0001653	PMID:17332895	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0000256	PMID:17332895	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:614651	Coenzyme Q10 deficiency, primary, 2		HP:0001513	PMID:17332895	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-20]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000286	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000175	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0001770	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0002059	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000199	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0004322	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0001156	OMIM:258860	TAS					P	HPO:skoehler[2015-04-05]
OMIM:258860	Orofaciodigital syndrome IV		HP:0002132	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0001161	OMIM:258860	TAS					P	HPO:probinson[2015-02-22]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000180	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000191	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0011802	PMID:22883145	PCS					P	HPO:probinson[2015-02-22]
OMIM:258860	Orofaciodigital syndrome IV		HP:0100259	OMIM:258860	IEA					P	HPO:skoehler[2018-10-08]
OMIM:258860	Orofaciodigital syndrome IV		HP:0009381	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0001829	OMIM:258860	TAS					P	HPO:probinson[2015-02-22]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000316	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000767	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000007	OMIM:258860	TAS					I	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000218	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0030084	OMIM:258860	TAS					P	HPO:skoehler[2014-09-21]
OMIM:258860	Orofaciodigital syndrome IV		HP:0005736	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000347	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:258860	Orofaciodigital syndrome IV		HP:0000369	OMIM:258860	TAS					P	HPO:probinson[2009-02-17]
OMIM:614889	Immunodeficiency 28		HP:0011274	OMIM:614889	TAS					P	HPO:probinson[2015-05-12]
OMIM:614889	Immunodeficiency 28		HP:0000007	OMIM:614889	TAS					I	HPO:probinson[2015-05-12]
OMIM:614889	Immunodeficiency 28		HP:0002721	OMIM:614889	IEA					P	HPO:skoehler[2015-07-29]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000121	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000011	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0008936	PMID:27557811	PCS		1/1			P	HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0003577	PMID:27557811	PCS		1/1			C	HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0002266	PMID:27557811	PCS		1/1			P	HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0001263	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0003186	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0012389	PMID:27557811	PCS		1/1			P	HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000518	PMID:27557811	PCS	HP:0011463	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000639	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000007	PMID:27557811	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000348	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0001258	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000369	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0000358	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:617370	Peroxisome biogenesis disorder 10B		HP:0001347	PMID:27557811	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-03]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0002257	PMID:22581229	PCS		4/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0012265	PMID:22581229	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0003577	PMID:22581229	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0001696	PMID:22581229	PCS		4/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0012255	PMID:22581229	PCS		6/6			P	HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0001651	PMID:22581229	PCS		3/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0002110	PMID:22581229	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0000007	PMID:22581229	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0012735	PMID:22581229	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0000403	PMID:22581229	PCS		1/11			P	HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0011109	PMID:22581229	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:614679	Ciliary dyskinesia, primary, 17		HP:0002205	PMID:22581229	PCS		5/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:613116	Thrombophilia due to histidine-rich glycoprotein deficiency		HP:0004831	OMIM:613116	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613116	Thrombophilia due to histidine-rich glycoprotein deficiency		HP:0003581	PMID:9414276	PCS		1/1			C	HPO:probinson[2023-01-30]
OMIM:613116	Thrombophilia due to histidine-rich glycoprotein deficiency		HP:0100724	OMIM:613116	TAS					P	HPO:probinson[2013-01-09]
OMIM:613116	Thrombophilia due to histidine-rich glycoprotein deficiency		HP:0001977	OMIM:613116	TAS					P	HPO:probinson[2013-06-02]
OMIM:613116	Thrombophilia due to histidine-rich glycoprotein deficiency		HP:0040227	PMID:9414276	PCS		1/1			P	HPO:probinson[2023-01-30];HPO:probinson[2023-01-30]
OMIM:613116	Thrombophilia due to histidine-rich glycoprotein deficiency		HP:0000006	PMID:9414276	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2023-01-30]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000486	PMID:26647308	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0002463	PMID:25131622	PCS		1/1			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0001531	PMID:24214399	PCS		1/1			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0002188	PMID:25131622	PCS		1/1			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0003196	PMID:26647308	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0003593	PMID:20950788;PMID:26647308	PCS		5/5			C	HPO:probinson[2020-12-13];HPO:probinson[2022-07-19]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0001290	PMID:26647308	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0001270	PMID:26647308	PCS		3/3			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000639	PMID:26647308	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0011220	PMID:24214399	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000718	PMID:26647308	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000739	PMID:26647308	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000316	PMID:26647308	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000733	PMID:20950788	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0008872	PMID:24214399	PCS		1/1			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000455	PMID:24214399	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000278	PMID:26647308	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000256	PMID:26647308;PMID:25131622	PCS		2/4			P	HPO:probinson[2020-12-13];HPO:skoehler[2014-11-26];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0001249	PMID:20950788;PMID:25131622	PCS		3/3			P	HPO:skoehler[2013-06-16];HPO:probinson[2020-12-13];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000732	PMID:20950788	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000494	PMID:24214399	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000750	PMID:24214399;PMID:20950788;PMID:26647308	PCS		5/5		HP:0012828	P	HPO:probinson[2020-12-13];HPO:skoehler[2014-11-26];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0031936	PMID:24214399	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000194	OMIM:613670	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0001263	PMID:24214399;PMID:20950788;PMID:25131622	PCS		4/4			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000272	PMID:24214399	PCS		1/1			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0002194	PMID:24214399	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0011298	PMID:24214399	PCS		1/1			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000729	PMID:26647308	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0011098	PMID:26647308	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000805	PMID:26647308	PCS		1/3			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000722	PMID:26647308	PCS		3/3			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0100716	PMID:20950788	PCS		2/2			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0002307	PMID:24214399	PCS		1/1			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0007018	PMID:26647308	PCS		2/3			P	HPO:probinson[2020-12-13]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0001513	OMIM:613670	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:613670	Intellectual developmental disorder with language impairment with or without autistic features		HP:0000006	PMID:20950788	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-13]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0000750	PMID:31649809	PCS		7/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001250	PMID:31649809	PCS		4/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001263	PMID:31649809	IEA		7/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001290	PMID:31649809	PCS		3/6			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001182	PMID:31649809	PCS		3/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0000729	PMID:31649809	PCS		3/6			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0000739	PMID:31649809	PCS		4/5			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001999	PMID:31649809	PCS					P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0004209	PMID:31649809	PCS		4/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001357	PMID:31649809	PCS		1/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001159	PMID:31649809	PCS		2/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0000256	PMID:31649809	PCS		2/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0007018	PMID:31649809	PCS		4/5			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0000006	PMID:31649809	PCS					I	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001249	PMID:31649809	PCS		7/7			P	HPO:probinson[2020-07-14]
OMIM:618725	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures		HP:0001513	PMID:31649809	PCS		4/7			P	HPO:probinson[2020-07-14]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0002366	OMIM:611067	TAS					P	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0003697	OMIM:611067	TAS					P	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0003445	OMIM:611067	TAS					P	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0001762	OMIM:611067	IEA					P	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0002650	OMIM:611067	IEA					P	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0001288	OMIM:611067	TAS					P	HPO:probinson[2012-05-26]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0003693	OMIM:611067	TAS					P	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0003551	OMIM:611067	TAS					P	HPO:probinson[2012-05-26]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0001284	OMIM:611067	IEA					P	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0002460	OMIM:611067	TAS					P	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0011463	OMIM:611067	TAS					C	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0009473	OMIM:611067	TAS					P	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0000007	OMIM:611067	IEA					I	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0002515	OMIM:611067	IEA					P	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0003307	OMIM:611067	IEA					P	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0002747	OMIM:611067	IEA					P	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0007269	OMIM:611067	TAS					P	HPO:probinson[2012-04-11]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0003701	OMIM:611067	IEA					P	HPO:iea[2009-02-17]
OMIM:611067	Spinal muscular atrophy, distal, autosomal recessive, 4		HP:0003678	OMIM:611067	IEA					C	HPO:iea[2009-02-17]
OMIM:609628	Majeed syndrome		HP:0003565	PMID:27252506;PMID:10969284	PCS		6/6			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0001386	PMID:27252506	PCS	HP:0011463	2/2			P	HPO:probinson[2020-10-26];HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0002653	PMID:15994876	PCS		6/6			P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0025066	PMID:10969284	PCS					P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0002750	PMID:10969284	PCS		4/4			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0001371	PMID:15994876	PCS					P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0010972	PMID:15994876	PCS					P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0012132	PMID:27252506;PMID:10969284	PCS		11/11			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0011123	PMID:15994876	PCS					P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0002829	PMID:15994876	PCS		6/6			P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0001508	PMID:10969284	PCS		4/4			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0000007	PMID:15994876	PCS					I	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0001954	PMID:15994876	PCS		6/6			P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0001935	PMID:15994876	PCS		6/6			P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0001935	PMID:10969284	PCS		4/4			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0001935	PMID:27252506	PCS	HP:0011463	1/2			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0000823	PMID:27252506	PCS		1/2			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0000988	PMID:15994876	PCS		2/6			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0001510	PMID:15994876	PCS					P	HPO:probinson[2017-06-23]
OMIM:609628	Majeed syndrome		HP:0001433	PMID:27252506;PMID:10969284	PCS		5/6			P	HPO:probinson[2020-10-26]
OMIM:609628	Majeed syndrome		HP:0002754	PMID:15994876	PCS					P	HPO:probinson[2017-06-23]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000483	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000365	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000486	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0001250	PMID:26264232	PCS		2/6			P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0003593	OMIM:616708	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0001290	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000280	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0011220	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000718	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000739	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000316	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000414	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000337	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000219	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0002714	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000713	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0002019	PMID:26264232	PCS		5/6			P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000377	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0001007	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000358	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000574	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000750	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0002079	OMIM:616708	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0011968	PMID:26264232	PCS		4/6			P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000293	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000490	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0001263	PMID:26264232	PCS		6/6			P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0003186	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000470	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0011800	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0005280	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000708	PMID:26264232	PCS		5/6			P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000407	OMIM:616708	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000664	PMID:26264232	PCS					P	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0007018	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000006	PMID:26264232	PCS					I	HPO:probinson[2017-06-17]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000545	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616708	Desanto-Shinawi syndrome		HP:0000248	OMIM:616708	TAS					P	HPO:skoehler[2017-07-13]
OMIM:150260	Laryngeal abductor paralysis		HP:0000252	OMIM:150260	IEA					P	HPO:iea[2009-02-17]
OMIM:150260	Laryngeal abductor paralysis		HP:0002015	OMIM:150260	IEA					P	HPO:skoehler[2010-06-20]
OMIM:150260	Laryngeal abductor paralysis		HP:0001762	OMIM:150260	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:150260	Laryngeal abductor paralysis		HP:0010307	OMIM:150260	IEA					P	HPO:skoehler[2010-06-20]
OMIM:150260	Laryngeal abductor paralysis		HP:0001609	OMIM:150260	IEA					P	HPO:skoehler[2019-02-22]
OMIM:150260	Laryngeal abductor paralysis		HP:0003593	OMIM:150260	IEA					C	HPO:skoehler[2019-02-22]
OMIM:150260	Laryngeal abductor paralysis		HP:0001605	OMIM:150260	IEA					P	HPO:iea[2009-02-17]
OMIM:150260	Laryngeal abductor paralysis		HP:0001621	OMIM:150260	IEA					P	HPO:skoehler[2019-02-22]
OMIM:150260	Laryngeal abductor paralysis		HP:0000961	OMIM:150260	IEA					P	HPO:skoehler[2019-09-07]
OMIM:150260	Laryngeal abductor paralysis		HP:0000006	OMIM:150260	IEA					I	HPO:iea[2009-02-17]
OMIM:150260	Laryngeal abductor paralysis		HP:0001249	OMIM:150260	IEA					P	HPO:iea[2009-02-17]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0004325	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000121	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000486	PMID:27023906	PCS		2/2			P	HPO:probinson[2023-06-10];HPO:probinson[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0004322	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0002021	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000160	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001252	PMID:28065471	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0010761	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0003391	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0012301	PMID:28065471	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000639	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000316	PMID:27023906;PMID:28065471	PCS		5/6			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001845	PMID:27023906	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000678	PMID:28065471	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001324	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001763	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001601	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001188	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0002751	PMID:28065471	PCS		2/4			P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001385	PMID:28065471	PCS		2/3			P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000054	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001382	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0011648	PMID:27023906	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0005180	PMID:27023906	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0012810	PMID:28065471	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0012385	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0034392	PMID:28065471	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0006380	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0034273	PMID:27023906	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0009099	PMID:28065471	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000327	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000007	PMID:27023906	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0003758	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0002108	PMID:28065471	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001659	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000444	PMID:27023906;PMID:28065471	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0009933	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0008689	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001015	PMID:27023906	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000369	PMID:28065471	PCS		4/4			P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000325	PMID:28065471	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001655	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0003577	PMID:27023906;PMID:28065471	PCS		6/6			C	ORCID:0000-0002-0736-9199[2024-04-22];HPO:probinson[2023-06-10];HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000343	PMID:28065471	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000463	PMID:28065471	PCS		2/2			P	HPO:probinson[2023-06-10];HPO:probinson[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0012727	PMID:28065471	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000581	PMID:27023906	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0011712	OMIM:617402	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0011120	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000218	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000455	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000973	PMID:27023906;PMID:28065471	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-22];HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001562	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001762	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0200128	OMIM:617402	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000350	PMID:27023906;PMID:28065471	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000272	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001519	PMID:28065471	PCS		2/4			P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000629	PMID:27023906	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000307	PMID:28065471	PCS		4/4			P	HPO:skoehler[2018-10-08]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001631	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000028	PMID:27023906	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000303	PMID:27023906	PCS		1/2			P	HPO:probinson[2023-06-10]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0001634	OMIM:617402	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617402	Cutis laxa, autosomal recessive, type IIC		HP:0000621	PMID:27023906;PMID:28065471	PCS		6/6			P	HPO:skoehler[2017-07-13];ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0001572	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0001792	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0002188	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000486	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000463	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0001250	PMID:31256877	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0012469	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000639	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000618	PMID:31256877	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000316	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0002714	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000411	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0004558	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000252	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0009804	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000475	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0002650	PMID:31256877	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0001321	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0030048	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0001263	PMID:31256877	PCS		5/5			P	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0011800	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000508	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000602	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000007	PMID:31256877	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000307	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0001357	PMID:31256877	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000322	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0002126	PMID:31256877	PCS		2/5			P	HPO:probinson[2020-05-11]
OMIM:618731	Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies		HP:0000324	PMID:31256877	PCS		1/5			P	HPO:probinson[2020-05-11]
OMIM:223550	Dwarfism, proportionate, with hip dislocation		HP:0003510	OMIM:223550	IEA					P	HPO:iea[2009-02-17]
OMIM:223550	Dwarfism, proportionate, with hip dislocation		HP:0002827	OMIM:223550	IEA					P	HPO:iea[2009-02-17]
OMIM:223550	Dwarfism, proportionate, with hip dislocation		HP:0000007	OMIM:223550	IEA					I	HPO:iea[2009-02-17]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002345	OMIM:254900	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002202	PMID:18424452	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0000100	PMID:18424452	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0001272	OMIM:254900	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002066	OMIM:254900	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0000083	PMID:18424452	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0003073	PMID:18424452	PCS		2/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002080	OMIM:254900	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0100820	OMIM:254900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002317	PMID:18424452	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0012050	PMID:18424452	PCS		1/2			P	HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0001268	PMID:18424452	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002015	PMID:18424452	PCS		1/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0003621	PMID:18424452	PCS		1/2			C	HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0000112	OMIM:254900	IEA					P	HPO:iea[2009-02-17]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002197	OMIM:254900	IEA					P	HPO:iea[2009-02-17]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0001260	OMIM:254900	IEA					P	HPO:iea[2009-02-17]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0000097	OMIM:254900	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0002174	OMIM:254900	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0000093	PMID:18424452	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0025708	PMID:18424452	PCS		1/2			C	HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0000969	PMID:18424452	PCS		2/2			P	HPO:probinson[2023-02-20];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0000007	PMID:18308289	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0001895	PMID:18424452	PCS		2/2			P	HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0001873	PMID:18424452	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0001336	PMID:18424452	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-20]
OMIM:254900	Epilepsy, progressive myoclonic, 4, with or without renal failure		HP:0003678	PMID:18424452	PCS					C	HPO:skoehler[2013-05-31];HPO:probinson[2023-02-20]
OMIM:206920	Microphthalmia with limb anomalies		HP:0002982	PMID:21194678	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0003038	PMID:21194678	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001770	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0003577	PMID:21194678	PCS		4/4			C	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0002002	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000581	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0003196	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0012745	OMIM:206920	TAS					P	HPO:skoehler[2014-03-24]
OMIM:206920	Microphthalmia with limb anomalies		HP:0012741	PMID:21194678	PCS		1/2			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0009380	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001849	OMIM:206920;PMID:21194678	PCS		13/14			P	HPO:probinson[2023-02-10];HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001508	PMID:21194678	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0011220	OMIM:206920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0005709	PMID:21194678	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000954	PMID:21194678	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0008897	OMIM:206920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000218	PMID:21194678	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000499	PMID:21194678	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000454	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000278	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0005867	PMID:21194678	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001249	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000358	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000175	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000494	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001440	PMID:21194678	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001762	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0010715	PMID:21194678	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001162	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001241	PMID:21194678	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001263	PMID:21194678	PCS		3/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0005280	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0008081	PMID:21194678	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000528	PMID:21194678	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0002827	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0011671	OMIM:206920	TAS					P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000007	PMID:21194678	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000568	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0002007	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001830	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001852	PMID:21194678	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001510	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000960	PMID:21194678	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000204	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0000369	OMIM:206920	IEA					P	HPO:iea[2009-02-17]
OMIM:206920	Microphthalmia with limb anomalies		HP:0001215	PMID:21194678	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:219800	Cystinosis, nephropathic		HP:0002344	OMIM:219800	TAS					P	HPO:skoehler[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0001531	PMID:35513889	PCS	HP:0003593	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0032639	PMID:24464559	PCS		15/15			P	HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0004322	PMID:24464559	PCS	HP:0003593	15/15			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0003234	OMIM:219800	TAS					P	HPO:skoehler[2013-11-18]
OMIM:219800	Cystinosis, nephropathic		HP:0003355	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0003198	PMID:21900880	PCS	HP:0011462	22/86			P	HPO:lccarmody[2009-02-17];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0000083	PMID:20803298;PMID:24464559	PCS		28/38			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-16];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0001010	PMID:35513889	PCS		2/2			P	HPO:probinson[2013-03-12];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0003593	PMID:35513889;PMID:24464559;PMID:31672123	PCS		18/18			C	HPO:probinson[2022-03-28];HPO:probinson[2022-05-20];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0003076	PMID:35513889;PMID:31672123	PCS		3/3			P	HPO:probinson[2022-05-20];HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0000832	PMID:24464559	PCS	HP:0011463	4/15			P	HPO:lccarmody[2018-06-19];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0003109	PMID:35513889;PMID:31672123	PCS		3/3			P	HPO:probinson[2022-03-28];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0002857	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0004912	PMID:35513889;PMID:31672123	PCS		2/3			P	HPO:probinson[2022-05-20];HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0004911	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0001249	PMID:32102670	PCS		0/17			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0003202	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0000495	OMIM:219800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219800	Cystinosis, nephropathic		HP:0003126	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0002750	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0001263	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0000093	PMID:35513889	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0002909	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0002907	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0001738	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0002748	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0002748	PMID:24464559	PCS	HP:0003593	13/15			P	HPO:lccarmody[2018-06-19];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0002902	PMID:35513889	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0000007	PMID:12110740	PCS					I	HPO:lccarmody[2016-06-19]
OMIM:219800	Cystinosis, nephropathic		HP:0002900	PMID:35513889;PMID:31672123	PCS		3/3			P	HPO:probinson[2022-03-28];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0000966	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0000488	OMIM:219800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:219800	Cystinosis, nephropathic		HP:0002148	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0003358	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0030190	PMID:2381441	PCS					P	HPO:lccarmody[2018-06-19]
OMIM:219800	Cystinosis, nephropathic		HP:0003774	PMID:35513889	PCS	HP:0003621	2/2			P	HPO:lccarmody[2018-06-19];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0007814	PMID:16603246	PCS					P	HPO:probinson[2015-07-19]
OMIM:219800	Cystinosis, nephropathic		HP:0003016	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0005599	PMID:35513889	PCS		2/2			P	HPO:probinson[2013-03-12];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0031969	PMID:35513889	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0012408	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0003251	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0000580	OMIM:219800	TAS					P	HPO:probinson[2015-07-19]
OMIM:219800	Cystinosis, nephropathic		HP:0002240	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0000819	PMID:35997069	PCS	HP:0003581	6/13			P	HPO:lccarmody[2009-02-17];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0002917	PMID:35513889	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0001508	PMID:20803298	PCS		19/23			P	HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0000618	PMID:11116719	PCS	HP:0011462	1/1			P	HPO:lccarmody[2018-06-19];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0000618	PMID:20803298	PCS		0/23			P	HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0000613	PMID:12110740	PCS	HP:0003621				P	HPO:lccarmody[2009-02-17];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0001944	PMID:35513889	PCS	HP:0003593	2/2			P	HPO:lccarmody[2010-06-20];HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0007663	PMID:12110740	PCS					P	HPO:skoehler[2015-07-26]
OMIM:219800	Cystinosis, nephropathic		HP:0001824	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0000531	PMID:11001803;PMID:35513889;PMID:24464559	PCS		187/187			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-20];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0002514	PMID:21900880	PCS	HP:0003581	9/33			P	HPO:lccarmody[2018-06-19];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0001744	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0000897	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0001942	PMID:35513889;PMID:24464559;PMID:31672123	PCS		11/18			P	HPO:probinson[2022-03-28];HPO:probinson[2022-05-20];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0002015	PMID:30685240	PCS	HP:0003581				P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0002059	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:6001033	PMID:28871612	PCS		10/10			P	HPO:probinson[2024-08-04]
OMIM:219800	Cystinosis, nephropathic		HP:6001032	PMID:32727395	PCS					P	HPO:probinson[2024-08-04]
OMIM:219800	Cystinosis, nephropathic		HP:6001031	PMID:32727395	PCS					P	HPO:probinson[2024-08-04]
OMIM:219800	Cystinosis, nephropathic		HP:0000790	PMID:35513889	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0001959	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0001959	PMID:35513889	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:219800	Cystinosis, nephropathic		HP:0001959	PMID:35997069	PCS	HP:0003593	8/13			P	HPO:lccarmody[2009-02-17];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0000505	PMID:12110740	PCS					P	HPO:lccarmody[2016-06-19]
OMIM:219800	Cystinosis, nephropathic		HP:0000823	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0000103	PMID:35997069;PMID:31672123	PCS		9/14			P	HPO:probinson[2024-03-16];HPO:iea[2009-02-17];HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0000026	PMID:12110740	PCS	HP:0003581		MALE		P	HPO:lccarmody[2018-06-19];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0002007	OMIM:219800	IEA					P	HPO:iea[2009-02-17]
OMIM:219800	Cystinosis, nephropathic		HP:0001994	PMID:31672123	PCS		1/1			P	HPO:probinson[2022-03-28]
OMIM:219800	Cystinosis, nephropathic		HP:0001994	PMID:24464559	PCS	HP:0003593	14/15			P	HPO:lccarmody[2009-02-17];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0001510	PMID:35997069	PCS		10/13			P	HPO:lccarmody[2018-06-19];HPO:probinson[2024-03-16]
OMIM:219800	Cystinosis, nephropathic		HP:0000787	PMID:35513889	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-20]
OMIM:227050	Transient erythroblastopenia of childhood		HP:0005510	OMIM:227050	IEA					P	HPO:iea[2009-02-17]
OMIM:227050	Transient erythroblastopenia of childhood		HP:0001903	OMIM:227050	IEA					P	HPO:iea[2009-02-17]
OMIM:227050	Transient erythroblastopenia of childhood		HP:0000007	OMIM:227050	IEA					I	HPO:iea[2009-02-17]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0000164	PMID:19765682	PCS		0/4			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0003115	PMID:19765682	PCS		0/4			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0002231	PMID:19765682	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-07-04];HPO:probinson[2021-10-05]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0003593	PMID:19765682	PCS		4/4			C	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0025092	PMID:31790667	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0045075	PMID:19765682;PMID:31790667	PCS		5/5			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0030318	PMID:31790667	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0008070	PMID:31790667	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0008066	PMID:31790667	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0200037	PMID:19765682	PCS		4/4			P	HPO:probinson[2013-06-02];HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0002209	PMID:19765682;PMID:31790667	PCS		5/5			P	HPO:probinson[2021-07-04];HPO:skoehler[2013-06-03];HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0000007	PMID:19765682	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0000653	PMID:19765682	PCS		4/4			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0007502	PMID:31790667	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0002215	PMID:19765682	PCS		4/4			P	HPO:skoehler[2013-06-03];HPO:probinson[2021-07-04];HPO:probinson[2021-10-05]
OMIM:613102	Hypotrichosis and recurrent skin vesicles		HP:0001820	PMID:31790667	PCS		1/1			P	HPO:probinson[2021-07-04]
OMIM:615573	Nephrotic syndrome, type 9		HP:0003774	PMID:24270420	PCS		9/9			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0003676	PMID:24270420	PCS					C	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0003621	PMID:24270420	PCS		8/15			C	HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0000097	PMID:24270420	PCS		12/13			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0003593	PMID:24270420	PCS		1/15			C	HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0000096	PMID:24270420	PCS		1/15			P	HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0003073	PMID:24270420	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0000093	PMID:24270420	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0012588	PMID:24270420	PCS		15/15			P	HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0000969	PMID:24270420	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0011463	PMID:24270420	PCS		1/15			C	HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0011462	PMID:24270420	PCS		5/15			C	HPO:probinson[2023-02-26]
OMIM:615573	Nephrotic syndrome, type 9		HP:0000007	PMID:24270420	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-26]
OMIM:301083	Hemolytic anemia due to elevated adenosine deaminase		HP:0012132	PMID:3164080	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:301083	Hemolytic anemia due to elevated adenosine deaminase		HP:0004446	PMID:3164080	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:301083	Hemolytic anemia due to elevated adenosine deaminase		HP:0001419	PMID:35030251	PCS					I	HPO:probinson[2022-08-06]
OMIM:301083	Hemolytic anemia due to elevated adenosine deaminase		HP:0002904	PMID:3164080	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:301083	Hemolytic anemia due to elevated adenosine deaminase		HP:0001878	PMID:3164080	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:301083	Hemolytic anemia due to elevated adenosine deaminase		HP:4000184	PMID:3164080	PCS		1/1			P	HPO:probinson[2023-06-05]
OMIM:301083	Hemolytic anemia due to elevated adenosine deaminase		HP:0001923	PMID:3164080	PCS		1/1			P	HPO:probinson[2022-08-06]
OMIM:608244	Otosclerosis 3		HP:0000362	OMIM:608244	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608244	Otosclerosis 3		HP:0000365	OMIM:608244	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608244	Otosclerosis 3		HP:0003829	OMIM:608244	IEA					I	HPO:skoehler[2010-06-19]
OMIM:608244	Otosclerosis 3		HP:0000006	OMIM:608244	IEA					I	HPO:skoehler[2010-06-19]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0003577	PMID:27479907	PCS		3/3			C	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000463	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0010747	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0001290	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0001808	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000958	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000639	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0005709	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0001328	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0006695	PMID:27479907	PCS		2/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0001869	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000252	PMID:27479907	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000750	PMID:27479907	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0002650	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0011968	PMID:27479907	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0001263	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000691	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0005280	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0011304	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0009890	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000426	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0002209	PMID:27479907	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0006323	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0002007	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0007018	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000006	PMID:27479907	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000963	PMID:27479907	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000248	PMID:27479907	PCS		1/3			P	HPO:probinson[2022-12-18]
OMIM:617364	Congenital heart defects and ectodermal dysplasia		HP:0000687	PMID:27479907	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:618057	Drug metabolism, altered, CES1-related		HP:0020169	PMID:18485328	PCS					P	HPO:probinson[2021-03-13]
OMIM:618057	Drug metabolism, altered, CES1-related		HP:0000006	PMID:18485328	PCS					I	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0002850	OMIM:611926	TAS					P	HPO:probinson[2012-07-26]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0001684	OMIM:611926	TAS					P	HPO:probinson[2012-07-26]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0000133	OMIM:611926	IEA					P	HPO:skoehler[2015-01-27]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0030813	OMIM:611926	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0100765	OMIM:611926	TAS					P	HPO:probinson[2012-07-26]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0000007	OMIM:611926	IEA					I	HPO:iea[2009-02-17]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0000777	OMIM:611926	TAS					P	HPO:probinson[2012-07-26]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0002206	OMIM:611926	IEA					P	HPO:skoehler[2010-06-20]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0002720	OMIM:611926	TAS					P	HPO:probinson[2012-07-26]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0005415	OMIM:611926	TAS					P	HPO:probinson[2012-07-26]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0004315	OMIM:611926	TAS					P	HPO:probinson[2012-07-26]
OMIM:611926	Immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis		HP:0002721	OMIM:611926	IEA					P	HPO:skoehler[2015-01-27]
OMIM:300376	Muscular dystrophy, Becker type		HP:0001265	OMIM:300376	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0003236	OMIM:300376	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0003115	OMIM:300376	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300376	Muscular dystrophy, Becker type		HP:0001419	OMIM:300376	TAS					I	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0003581	OMIM:300376	TAS					C	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0003707	OMIM:300376	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0003560	OMIM:300376	IEA					P	HPO:skoehler[2015-01-21]
OMIM:300376	Muscular dystrophy, Becker type		HP:0001638	OMIM:300376	TAS	HP:0003584				P	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0011675	OMIM:300376	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0001324	OMIM:300376	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300376	Muscular dystrophy, Becker type		HP:0003326	OMIM:300376	TAS					P	HPO:skoehler[2012-10-14]
OMIM:301068	Hardikar syndrome		HP:0001410	PMID:18348269	PCS		4/4			P	HPO:probinson[2022-02-05];HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001971	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0004322	PMID:18348269	PCS		3/4			P	HPO:probinson[2022-02-05];HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000083	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0100333	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001409	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001408	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0005209	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001643	PMID:18348269	PCS		2/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000952	PMID:18348269	PCS		4/4			P	HPO:probinson[2022-02-05];HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000010	PMID:18348269	PCS		4/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0011968	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0005343	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0100336	PMID:18348269	PCS		2/4			P	HPO:probinson[2024-03-08]
OMIM:301068	Hardikar syndrome		HP:0031082	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0100337	PMID:18348269	PCS		2/4			P	HPO:probinson[2024-03-08]
OMIM:301068	Hardikar syndrome		HP:0100334	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002904	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001537	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0030151	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002944	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0007678	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002027	PMID:18348269	PCS		2/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000126	PMID:18348269	PCS		4/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001655	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001396	PMID:18348269	PCS		2/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0004467	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001399	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002321	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000185	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0030353	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001395	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001394	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002240	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000580	PMID:18348269	PCS		4/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002040	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0033149	PMID:18348269	PCS		4/4			P	HPO:probinson[2022-02-05];HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0031766	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0012330	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000939	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0033196	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001508	PMID:18348269	PCS		2/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001629	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000737	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002836	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001423	PMID:33244166	PCS					I	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002910	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001788	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0006579	PMID:18348269	PCS		3/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0004415	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001744	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000076	PMID:18348269	PCS		2/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0030169	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002013	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000072	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001680	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0012712	PMID:18348269	PCS		2/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0010773	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002608	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000822	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0000989	PMID:18348269	PCS		2/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001631	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001510	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001433	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0001873	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002566	PMID:18348269	PCS		4/4			P	HPO:probinson[2022-02-05]
OMIM:301068	Hardikar syndrome		HP:0002248	PMID:18348269	PCS		1/4			P	HPO:probinson[2022-02-05]
OMIM:606282	Deafness, autosomal dominant 24		HP:0000365	OMIM:606282	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606282	Deafness, autosomal dominant 24		HP:0000006	OMIM:606282	TAS					I	HPO:skoehler[2017-07-13]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0003577	PMID:24207119	PCS		7/13			C	HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0003621	PMID:24207119	PCS		2/13			C	HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0025114	OMIM:615598	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0011463	PMID:24207119	PCS		1/13			C	HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0003593	PMID:24207119	PCS		2/13			C	HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0025092	OMIM:615598	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0000007	PMID:24207119	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0025080	OMIM:615598	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0007410	PMID:24207119	PCS		11/13			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0000972	PMID:24207119	PCS		13/13			P	HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0032007	PMID:24207119	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:615598	Palmoplantar keratoderma, Nagashima type		HP:0003623	PMID:24207119	PCS		1/13			C	HPO:probinson[2023-03-05]
OMIM:304110	Craniofrontonasal syndrome		HP:0011939	PMID:15124102	PCS		1/5			P	HPO:probinson[2024-07-22]
OMIM:304110	Craniofrontonasal syndrome		HP:0000164	OMIM:304110	TAS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:304110	Craniofrontonasal syndrome		HP:0001770	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0004322	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0004440	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001252	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001290	OMIM:304110	TAS					P	HPO:skoehler[2017-07-13]
OMIM:304110	Craniofrontonasal syndrome		HP:0001809	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001808	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000639	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0010055	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001807	PMID:15124102	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000316	PMID:15124102	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000912	PMID:15124102	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0200021	OMIM:304110	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304110	Craniofrontonasal syndrome		HP:0001249	PMID:15124102	PCS		0/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000175	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000494	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0002079	PMID:15124102	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0001382	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001263	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0012813	PMID:15124102	PCS		1/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0001060	OMIM:304110	IEA		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000767	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001537	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0006585	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0004209	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000047	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000248	OMIM:304110	IEA		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000204	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000324	OMIM:304110	IEA		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000049	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001156	OMIM:304110	IEA		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0005278	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001274	OMIM:304110	IEA		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0002162	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001547	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0001423	PMID:15124102	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000776	OMIM:304110	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304110	Craniofrontonasal syndrome		HP:0000456	OMIM:304110	IEA		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000577	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0002212	PMID:15124102	PCS		1/5			P	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0002650	PMID:15124102	PCS		1/5			P	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000431	PMID:15124102	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0003187	OMIM:304110	IEA					P	HPO:skoehler[2010-06-20]
OMIM:304110	Craniofrontonasal syndrome		HP:0000470	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000506	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000349	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0002007	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:304110	Craniofrontonasal syndrome		HP:0000465	PMID:15124102	PCS		1/5			P	HPO:probinson[2023-04-08]
OMIM:304110	Craniofrontonasal syndrome		HP:0000028	OMIM:304110	TAS					P	HPO:skoehler[2014-03-24]
OMIM:304110	Craniofrontonasal syndrome		HP:0200053	OMIM:304110	IEA					P	HPO:iea[2009-02-17]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000365	PMID:9545394	PCS		4/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0004322	PMID:9545394;PMID:17461801	PCS		4/7			P	HPO:probinson[2020-10-04];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0100490	PMID:18940313	PCS		7/7			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0100651	PMID:17461801	IEA		3/4			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0012785	PMID:9545394	PCS		4/4			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0100694	PMID:18940313	PCS		4/8			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0009183	PMID:19175903	PCS		2/2			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0002619	PMID:18940313;PMID:19175903;PMID:18410979	PCS		11/19			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000953	PMID:18940313;PMID:17461801	PCS		9/12			P	HPO:probinson[2020-10-04];HPO:probinson[2020-10-04];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0100727	PMID:9545394	PCS		4/4			P	HPO:skoehler[2015-01-21];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001643	PMID:18940313	PCS	HP:0003577	1/8			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000278	PMID:19175903	PCS		1/2			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001642	PMID:18940313	PCS		1/8			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001763	PMID:17461801	PCS		2/4			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0003565	PMID:16118898	PCS		3/3			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000054	PMID:18940313;PMID:18410979	PCS		6/12	MALE		P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000494	PMID:19175903	PCS		1/2			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000771	PMID:18410979	PCS		3/3	MALE		P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000771	PMID:19175903	PCS		1/2			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0002594	OMIM:602782	TAS		HP:0040284			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0100534	PMID:17461801;PMID:18410979	PCS		8/14			P	HPO:probinson[2020-10-04];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0012385	PMID:18410979	PCS		2/10			P	HPO:skoehler[2013-10-22];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000407	PMID:18940313;PMID:16118898	PCS		8/11			P	HPO:skoehler[2012-11-21];HPO:probinson[2020-10-04];HPO:probinson[2020-10-04];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000007	PMID:9545394	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000520	PMID:18940313;PMID:17461801;PMID:18410979	PCS		8/21			P	HPO:probinson[2020-10-04];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0002987	OMIM:602782	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0005830	PMID:9545394	PCS		4/4			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000463	PMID:19175903	PCS		1/2			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0025289	PMID:9545394;PMID:16118898	PCS		12/13			P	HPO:probinson[2020-10-04];HPO:skoehler[2017-07-13];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0002240	PMID:18940313;PMID:19175903;PMID:18410979;PMID:16118898	PCS		13/23			P	HPO:probinson[2020-10-04];HPO:probinson[2020-10-04];HPO:probinson[2020-10-04];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0007380	PMID:18940313;PMID:18410979	PCS		10/18			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001629	PMID:18410979	PCS		1/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000815	PMID:18410979	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0002716	PMID:9545394;PMID:19889517	PCS		12/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001822	PMID:18940313	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001945	PMID:16118898	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0030084	PMID:17461801	PCS		2/4			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0033190	PMID:18410979	PCS		10/10			P	HPO:probinson[2020-10-13]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001744	PMID:19175903;PMID:18410979	PCS		8/12			P	HPO:probinson[2020-10-04];HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001640	PMID:18410979	PCS		1/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0005200	OMIM:602782	TAS		HP:0040284			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001084	PMID:18940313;PMID:19175903	PCS		4/10			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0002293	PMID:19175903	PCS		1/2			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0002092	PMID:18940313;PMID:18410979	PCS		2/18			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001838	PMID:18940313	PCS		1/8			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0011670	PMID:18940313	PCS	HP:0003577	1/8			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000824	PMID:18410979	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001433	PMID:17461801	PCS		3/4			P	HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001631	PMID:18410979	PCS		2/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0001634	PMID:18410979	PCS		2/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-04]
OMIM:602782	Histiocytosis-lymphadenopathy plus syndrome		HP:0000027	PMID:18410979	PCS		3/3	MALE		P	HPO:probinson[2020-10-04]
OMIM:613857	Orofacial cleft 13		HP:0000185	PMID:21295280	PCS		3/3			P	HP:probinson[2018-07-10]
OMIM:613857	Orofacial cleft 13		HP:0000272	PMID:21295280	PCS		3/3			P	HP:probinson[2018-07-10]
OMIM:613857	Orofacial cleft 13		HP:0000278	PMID:21295280	PCS		3/3			P	HP:probinson[2018-07-10]
OMIM:613857	Orofacial cleft 13		HP:0000006	PMID:21295280	PCS					I	HPO:skoehler[2012-10-17]
OMIM:613857	Orofacial cleft 13		HP:0000347	PMID:21295280	PCS		3/3			P	HP:probinson[2018-07-10]
OMIM:613857	Orofacial cleft 13		HP:0000677	PMID:21295280	PCS					P	HP:probinson[2018-07-10]
OMIM:612591	Colorectal cancer, susceptibility to, 10		HP:0006716	PMID:23263490	PCS					P	HPO:probinson[2023-03-26]
OMIM:612591	Colorectal cancer, susceptibility to, 10		HP:0003581	PMID:23263490	PCS					C	HPO:probinson[2023-03-26]
OMIM:612591	Colorectal cancer, susceptibility to, 10		HP:0012114	PMID:23263490	PCS					P	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-26]
OMIM:612591	Colorectal cancer, susceptibility to, 10		HP:0000006	PMID:23263490	PCS					I	HPO:skoehler[2013-02-25];HPO:probinson[2023-03-26]
OMIM:612591	Colorectal cancer, susceptibility to, 10		HP:0200063	PMID:23263490	PCS					P	HPO:skoehler[2013-05-31];HPO:probinson[2023-03-26]
OMIM:270685	Spastic paraplegia 17		HP:0003621	PMID:23553728	PCS		1/1			C	HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0003431	PMID:23553728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0006858	PMID:23553728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0002166	OMIM:270685	IEA					P	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0003487	PMID:23553728	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0001761	PMID:23553728	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0003693	PMID:23553728	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0006937	PMID:23553728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0002460	PMID:23553728	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0002174	PMID:23553728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0002064	OMIM:270685	IEA					P	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0003392	OMIM:270685	IEA					P	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0002061	OMIM:270685	IEA					P	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0003393	OMIM:270685	IEA					P	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0001171	PMID:23553728	PCS		1/1			P	HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0007340	OMIM:270685	TAS					P	HPO:skoehler[2012-10-17]
OMIM:270685	Spastic paraplegia 17		HP:0003426	OMIM:270685	IEA					P	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0001258	PMID:23553728	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0003427	OMIM:270685	IEA					P	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0000006	PMID:14981520	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:270685	Spastic paraplegia 17		HP:0003677	OMIM:270685	IEA					C	HPO:iea[2009-02-17]
OMIM:270685	Spastic paraplegia 17		HP:0001347	PMID:23553728	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:607822	Alzheimer disease 3		HP:0002015	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0031868	OMIM:607822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607822	Alzheimer disease 3		HP:0001288	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0001332	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0002354	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0003487	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0001250	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0002120	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0002186	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0002395	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0001260	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0001285	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0003581	PMID:16033913	PCS					C	HPO:probinson[2012-07-22];HPO:probinson[2022-04-30]
OMIM:607822	Alzheimer disease 3		HP:0002185	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0002071	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0010524	OMIM:607822	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:607822	Alzheimer disease 3		HP:0000726	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0000751	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0000006	OMIM:607822	IEA					I	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0002511	OMIM:607822	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0001336	OMIM:607822	IEA					P	HPO:iea[2009-02-17]
OMIM:607822	Alzheimer disease 3		HP:0003678	OMIM:607822	IEA					C	HPO:iea[2009-02-17]
OMIM:600195	Venous malformations, multiple cutaneous and mucosal		HP:0002584	OMIM:600195	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600195	Venous malformations, multiple cutaneous and mucosal		HP:0000006	PMID:8980225	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:600195	Venous malformations, multiple cutaneous and mucosal		HP:0012721	PMID:10369874	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-31]
OMIM:620245	Episodic kinesigenic dyskinesia 3		HP:0000473	PMID:35707035	PCS		1/4		HP:0025228	P	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:620245	Episodic kinesigenic dyskinesia 3		HP:0003621	PMID:35707035;PMID:34518509	PCS		20/20			C	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:620245	Episodic kinesigenic dyskinesia 3		HP:0001332	PMID:35707035;PMID:34518509	PCS		17/21		HP:0025228;HP:0025228	P	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:620245	Episodic kinesigenic dyskinesia 3		HP:0001266	PMID:34518509	PCS		3/17		HP:0025228	P	HPO:probinson[2023-06-15]
OMIM:620245	Episodic kinesigenic dyskinesia 3		HP:0003829	PMID:35707035;PMID:34518509	PCS		20/20			I	HPO:probinson[2023-06-15]
OMIM:620245	Episodic kinesigenic dyskinesia 3		HP:0000006	PMID:34518509	PCS					I	HPO:probinson[2023-06-15]
OMIM:620245	Episodic kinesigenic dyskinesia 3		HP:0004305	PMID:35707035	PCS		3/4		HP:0025228	P	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0001276	PMID:32330417	PCS		3/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000154	PMID:32330417	PCS		3/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0002059	PMID:32330417	PCS		1/3		HP:0012825	P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0002521	PMID:32330417	PCS					P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0002188	PMID:32330417	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0002650	PMID:32330417	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0001250	PMID:32330417	PCS	HP:0003593	3/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0001263	PMID:32330417	IEA		3/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0010806	PMID:32330417	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0011800	PMID:32330417	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0011228	PMID:32330417	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0012469	PMID:32330417	PCS	HP:0003593	2/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0100023	PMID:32330417	PCS					P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000316	PMID:32330417	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000448	PMID:32330417	PCS		3/3			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000954	PMID:32330417	PCS				HP:0012834	P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000601	PMID:32330417	PCS		2/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000414	PMID:32330417	PCS		3/3			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000218	PMID:32330417	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000006	PMID:32330417	PCS					I	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0001249	PMID:32330417	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:618916	Epileptic encephalopathy, early infantile, 87		HP:0000687	PMID:32330417	PCS		3/3			P	HPO:probinson[2020-08-11]
OMIM:607836	Autoimmune disease, susceptibility to, 1		HP:0001045	PMID:16098053	PCS		13/14		HP:0012837	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:607836	Autoimmune disease, susceptibility to, 1		HP:0003621	PMID:16098053	PCS					C	HPO:probinson[2023-03-05]
OMIM:607836	Autoimmune disease, susceptibility to, 1		HP:0000872	PMID:16098053	PCS		7/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:607836	Autoimmune disease, susceptibility to, 1		HP:0000006	PMID:16098053	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-05]
OMIM:125600	Dermatosis papulosa nigra		HP:0000006	OMIM:125600	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:125600	Dermatosis papulosa nigra		HP:0000951	OMIM:125600	IEA					P	HPO:iea[2009-02-17]
OMIM:613843	Leber congenital amaurosis 15		HP:0001133	PMID:17962469	PCS		7/7			P	HPO:probinson[2015-07-19];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0003577	PMID:17962469	PCS		2/7			C	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000662	PMID:17962469	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000540	PMID:17962469	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000551	PMID:17962469	PCS		7/7			P	HPO:probinson[2015-07-19];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0030211	PMID:17962469	PCS		7/7			P	HPO:probinson[2015-07-19];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0001483	PMID:17962469	PCS		0/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000580	PMID:17962469	PCS					P	HPO:probinson[2015-07-19];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0003593	PMID:17962469	PCS		5/7			C	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0500087	PMID:17962469	PCS		3/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0034362	PMID:17962469	PCS		3/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0012047	PMID:17962469	PCS		7/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000639	PMID:17962469	PCS		7/7			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000613	PMID:17962469	PCS		0/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0007772	OMIM:613843	TAS					P	HPO:probinson[2015-07-19]
OMIM:613843	Leber congenital amaurosis 15		HP:0000546	PMID:17962469	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0007663	PMID:17962469	PCS		7/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000007	PMID:15024725	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000505	PMID:17962469	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0007787	PMID:17962469	PCS		3/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000543	PMID:17962469	PCS		2/7			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0007843	PMID:17962469	PCS		6/7			P	HPO:probinson[2023-01-31]
OMIM:613843	Leber congenital amaurosis 15		HP:0000545	PMID:17962469	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-31]
OMIM:312000	Panhypopituitarism, X-linked		HP:0000871	OMIM:312000	IEA					P	HPO:iea[2009-02-17]
OMIM:312000	Panhypopituitarism, X-linked		HP:0000839	OMIM:312000	IEA					P	HPO:iea[2009-02-17]
OMIM:312000	Panhypopituitarism, X-linked		HP:0001417	OMIM:312000	IEA					I	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0002240	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:6000536	OMIM:121300	TAS					P	HPO:probinson[2024-04-03]
OMIM:121300	Coproporphyria		HP:0011999	OMIM:121300	TAS					P	HPO:skoehler[2012-11-16]
OMIM:121300	Coproporphyria		HP:6000698	PMID:11929047	PCS		1/1			P	HPO:probinson[2024-05-09]
OMIM:121300	Coproporphyria		HP:0100785	OMIM:121300	TAS					P	HPO:skoehler[2012-11-16]
OMIM:121300	Coproporphyria		HP:0000716	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0000738	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0033010	PMID:12227458	PCS		4/4			P	HPO:probinson[2020-10-13];HPO:probinson[2020-11-26]
OMIM:121300	Coproporphyria		HP:0011462	PMID:12227458	PCS					C	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:121300	Coproporphyria		HP:0000739	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0003829	OMIM:121300	TAS					I	HPO:skoehler[2012-10-17]
OMIM:121300	Coproporphyria		HP:0001649	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0002019	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0000952	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0001744	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0002014	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0003489	PMID:12227458	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-26]
OMIM:121300	Coproporphyria		HP:0001289	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0000992	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0002013	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0003163	PMID:12227458	PCS		4/6			P	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26];HPO:probinson[2021-09-02]
OMIM:121300	Coproporphyria		HP:0012217	PMID:12227458	PCS		2/4			P	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:121300	Coproporphyria		HP:0034471	PMID:1733615	PCS					P	HPO:probinson[2022-12-18]
OMIM:121300	Coproporphyria		HP:0000822	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:121300	Coproporphyria		HP:0009830	OMIM:121300	TAS					P	HPO:probinson[2009-02-17]
OMIM:121300	Coproporphyria		HP:0002027	PMID:12227458	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-26]
OMIM:121300	Coproporphyria		HP:0000006	PMID:12227458	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-26]
OMIM:121300	Coproporphyria		HP:0002203	OMIM:121300	IEA					P	HPO:iea[2009-02-17]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0002069	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0002188	PMID:36307226	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0002121	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		1/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0001252	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		4/20			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0003593	PMID:35874597;PMID:23647072;PMID:36307226	PCS		19/21			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0032794	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		4/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0001270	PMID:35874597;PMID:23647072;PMID:36307226	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0032712	PMID:36307226	PCS		4/16			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0012469	PMID:35874597;PMID:23647072;PMID:32725632	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0011167	PMID:36307226	PCS		2/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0011463	PMID:36307226	PCS		1/17			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0020221	PMID:35874597;PMID:36307226	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0000158	PMID:32725632	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0001249	PMID:35874597;PMID:36307226;PMID:32725632	PCS		10/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0003623	PMID:32725632	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0006813	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		1/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0002059	PMID:36307226	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0000750	PMID:35874597;PMID:23647072;PMID:36307226	PCS		11/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0002133	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		3/22			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0002376	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		3/19			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0003584	PMID:36307226	PCS		1/17			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0001263	PMID:36307226	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0007099	PMID:36307226	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0000729	PMID:35874597;PMID:23647072	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0011153	PMID:36307226	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0030890	PMID:35874597;PMID:32725632	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0007334	PMID:35874597;PMID:23647072;PMID:36307226;PMID:32725632	PCS		6/21			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0200134	PMID:23647072;PMID:36307226;PMID:32725632	PCS		14/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0007018	PMID:36307226	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0007359	PMID:35874597;PMID:36307226	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0020217	PMID:36307226	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620537	Developmental and epileptic encephalopathy 112		HP:0000006	PMID:36307226	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0008935	OMIM:614862	TAS					P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0000582	PMID:8940266	PCS		1/1			P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0001250	OMIM:614862	TAS					P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0002240	PMID:8940266	PCS		1/1			P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0001290	PMID:8940266	PCS		1/1		HP:0012829	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-17]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0033643	PMID:8940266	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0005280	PMID:8940266	PCS		1/1			P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0010655	PMID:8940266	PCS		1/1			P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0034553	PMID:8940266	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0000107	OMIM:614862	TAS					P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0000316	PMID:8940266	PCS		1/1			P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0000007	PMID:8940266	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-02-17]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0008872	OMIM:614862	TAS					P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0002878	PMID:8940266	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0000537	PMID:8940266	PCS		1/1			P	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0001522	PMID:8940266	PCS		1/1			C	HPO:probinson[2013-02-24]
OMIM:614862	Peroxisome biogenesis disorder 4A (Zellweger)		HP:0003623	PMID:8940266	PCS		1/1			C	HPO:probinson[2023-02-17]
OMIM:301054	VEXAS syndrome, somatic		HP:0003596	PMID:33108101	IEA					C	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0030057	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0031688	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0031689	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0001907	PMID:33108101	PCS		11/25			P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0011123	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0200047	PMID:33108101	PCS		16/25			P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0001369	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0002113	PMID:33108101	PCS		18/25			P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0003565	PMID:33108101	PCS					P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0001442	PMID:33108101	PCS					I	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0030166	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0031234	PMID:33108101	PCS					P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0012378	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0011227	PMID:33108101	PCS					P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0012089	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0033380	PMID:33108101	PCS		16/25			P	HPO:probinson[2021-02-13]
OMIM:301054	VEXAS syndrome, somatic		HP:0002829	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0000407	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0001954	PMID:33108101	PCS		23/25			P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0200035	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0002625	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0001873	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0001972	PMID:33108101	PCS		24/25			P	HPO:probinson[2020-12-22]
OMIM:301054	VEXAS syndrome, somatic		HP:0002863	PMID:33108101	PCS					P	HPO:probinson[2020-12-22];HPO:probinson[2020-12-22]
OMIM:176270	Prader-Willi syndrome		HP:0000044	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000486	PMID:20301505	PCS					P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000046	PMID:20301505	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001773	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001531	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0003233	PMID:36793093	PCS		23/66			P	HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0004322	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001250	PMID:22585395;PMID:23824702	PCS		31/154			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08];HPO:probinson[2024-03-16]
OMIM:176270	Prader-Willi syndrome		HP:0003199	PMID:20301505	PCS	HP:0003581	HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001290	PMID:20301505	PCS	HP:0003623	HP:0040281			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0004283	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0012743	OMIM:176270	TAS					P	HPO:skoehler[2015-01-20]
OMIM:176270	Prader-Willi syndrome		HP:0011461	PMID:35160130	PCS		146/244			C	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000717	PMID:26331980	PCS		210/786			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001328	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0009466	OMIM:176270	TAS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000876	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002857	PMID:22043168	PCS					P	HP:probinson[2018-07-02]
OMIM:176270	Prader-Willi syndrome		HP:0005968	OMIM:176270	TAS		HP:0040283			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0003745	OMIM:176270	TAS					I	HPO:iea[2009-02-17]
OMIM:176270	Prader-Willi syndrome		HP:0001249	PMID:22585395	PCS		12/12			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-16]
OMIM:176270	Prader-Willi syndrome		HP:0007328	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0031878	PMID:22043168	PCS					P	HP:probinson[2018-07-02]
OMIM:176270	Prader-Willi syndrome		HP:0000054	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001385	PMID:29309382	PCS		27/90			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002155	PMID:36793093	PCS		10/66			P	HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0003124	PMID:36793093	PCS		42/66			P	HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002791	OMIM:176270	TAS					P	HPO:iea[2009-02-17]
OMIM:176270	Prader-Willi syndrome		HP:0002033	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002591	PMID:20301505	PCS	HP:0003593	HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002591	PMID:36793093	PCS		105/165			P	HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001263	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0003241	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001262	PMID:22585395	PCS		8/12			P	HPO:probinson[2024-03-16]
OMIM:176270	Prader-Willi syndrome		HP:0033454	PMID:35160130	PCS		216/244			P	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000969	PMID:22585395	PCS		9/12			P	HPO:probinson[2024-03-16]
OMIM:176270	Prader-Willi syndrome		HP:0000846	PMID:32443153	PCS		1/82			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0007874	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000565	PMID:20301505	PCS		HP:0040283			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0005978	PMID:35887798	PCS	HP:0011462	12/82			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0007513	OMIM:176270	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176270	Prader-Willi syndrome		HP:0000446	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000842	OMIM:176270	TAS					P	HPO:iea[2009-02-17]
OMIM:176270	Prader-Willi syndrome		HP:0000006	OMIM:176270	IEA					I	HPO:skoehler[2019-04-18]
OMIM:176270	Prader-Willi syndrome		HP:0001611	OMIM:176270	TAS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000341	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000582	OMIM:176270	TAS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0003577	PMID:35160130	PCS		98/244			C	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000540	OMIM:176270	TAS					P	HPO:iea[2009-02-17]
OMIM:176270	Prader-Willi syndrome		HP:0000064	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001270	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000060	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000939	PMID:22585395	PCS		2/12			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08];HPO:probinson[2024-03-16]
OMIM:176270	Prader-Willi syndrome		HP:0000938	PMID:20301505	PCS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0030919	PMID:35160130	PCS		14/244			P	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0030918	PMID:35160130	PCS		55/244			P	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0012450	PMID:22585395	PCS		5/12			P	HPO:probinson[2024-03-16]
OMIM:176270	Prader-Willi syndrome		HP:0008872	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002119	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000219	PMID:20301505;OMIM:176270	PCS		15/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002714	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0030084	OMIM:176270	TAS					P	HPO:skoehler[2014-09-21]
OMIM:176270	Prader-Willi syndrome		HP:0002236	OMIM:176270	TAS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001623	PMID:35160130	PCS		70/244			P	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0001562	PMID:35160130	PCS		16/244			P	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0001561	PMID:35160130	PCS	HP:0011461	57/244			P	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000670	OMIM:176270	TAS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0004279	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002650	PMID:35329900	PCS		150/180			P	HPO:iea[2010-10-08];HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000750	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000992	OMIM:176270	TAS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0010535	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000709	PMID:35887798	PCS		18/92			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000708	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000826	PMID:20301505	PCS					P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0007010	OMIM:176270	TAS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0002808	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000789	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001558	PMID:20301505	PCS		146/244			P	HPO:iea[2010-10-08];HPO:probinson[2022-05-14];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0100716	PMID:10349467	PCS		50/62			P	HPO:probinson[2021-05-06]
OMIM:176270	Prader-Willi syndrome		HP:0007015	OMIM:176270	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176270	Prader-Willi syndrome		HP:0001319	PMID:35160130	PCS		244/244			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000824	PMID:20301505	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000823	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0025501	PMID:36793093	PCS		90/165			P	HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001159	OMIM:176270	TAS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0200055	OMIM:176270	TAS					P	HPO:skoehler[2015-12-30]
OMIM:176270	Prader-Willi syndrome		HP:0002205	PMID:20301505	PCS		HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001511	PMID:35160130	PCS		50/244			P	HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000268	OMIM:176270	TAS					P	HPO:iea[2009-02-17]
OMIM:176270	Prader-Willi syndrome		HP:0007018	PMID:20301505	PCS	HP:0003593	HP:0040282			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0001513	PMID:35329900	PCS	HP:0011463	85/180			P	HPO:iea[2010-10-08];HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000545	PMID:20301505	PCS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:176270	Prader-Willi syndrome		HP:0000028	PMID:35160130	PCS		118/130			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:176270	Prader-Willi syndrome		HP:0000786	PMID:22585395	PCS		1/7			P	HPO:iea[2010-10-08];HPO:probinson[2024-03-08];HPO:probinson[2024-03-16]
OMIM:166705	Osteopoikilosis and dacryocystitis		HP:0010739	OMIM:166705	IEA					P	HPO:skoehler[2010-06-18]
OMIM:166705	Osteopoikilosis and dacryocystitis		HP:0000620	OMIM:166705	IEA					P	HPO:iea[2009-02-17]
OMIM:166705	Osteopoikilosis and dacryocystitis		HP:0000006	OMIM:166705	IEA					I	HPO:iea[2009-02-17]
OMIM:616913	Bleeding disorder, platelet-type, 20		HP:0000132	PMID:26280575	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:616913	Bleeding disorder, platelet-type, 20		HP:0000978	PMID:26280575	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:616913	Bleeding disorder, platelet-type, 20		HP:0000421	PMID:26280575	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:616913	Bleeding disorder, platelet-type, 20		HP:0001873	PMID:26280575	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:616913	Bleeding disorder, platelet-type, 20		HP:0000006	PMID:26280575	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:300438	HSD10 mitochondrial disease		HP:0002344	OMIM:300438	IEA		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-26]
OMIM:300438	HSD10 mitochondrial disease		HP:0002120	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0001250	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0001252	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0003593	OMIM:300438	IEA					C	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0001290	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0000639	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0000718	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0001943	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0000711	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0000713	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0001423	PMID:12696021	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-20]
OMIM:300438	HSD10 mitochondrial disease		HP:0001249	OMIM:300438	TAS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-26]
OMIM:300438	HSD10 mitochondrial disease		HP:0001942	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0003128	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0000572	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0002510	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0000750	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0001266	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0002376	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0001260	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0001263	OMIM:300438	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0001639	OMIM:300438	TAS					P	HPO:skoehler[2014-08-24]
OMIM:300438	HSD10 mitochondrial disease		HP:0000407	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0008322	OMIM:300438	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300438	HSD10 mitochondrial disease		HP:0000546	OMIM:300438	IEA					P	HPO:iea[2009-02-17]
OMIM:300438	HSD10 mitochondrial disease		HP:0000648	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300438	HSD10 mitochondrial disease		HP:0034290	PMID:12696021	PCS		5/5			P	HPO:probinson[2022-09-05]
OMIM:300438	HSD10 mitochondrial disease		HP:0001257	OMIM:300438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001297	PMID:16410789	PCS		1/16			P	HPO:iea[2009-02-17];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001297	PMID:23935882	PCS	HP:0003581	3/67			P	HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0012426	PMID:23577018	PCS					P	HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0032553	PMID:16410789	PCS		1/16			P	HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0033026	PMID:23762643	PCS					P	HPO:probinson[2020-06-09]
OMIM:264800	Pseudoxanthoma elasticum		HP:0033027	PMID:25526100	PCS	HP:0003621	9/9			P	HPO:probinson[2020-06-09]
OMIM:264800	Pseudoxanthoma elasticum		HP:0045051	PMID:27622520	PCS	HP:0003596	11/35			P	HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0007663	PMID:29652691	PCS		50/195			P	HPO:probinson[2012-07-16];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001723	PMID:3342167	PCS		HP:0040284			P	HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0004417	PMID:16410789	PCS		2/16			P	HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0004417	PMID:23968982	PCS	HP:0003581	2/26			P	HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0002239	PMID:16410789	PCS		5/16			P	HPO:iea[2009-02-17];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0000973	PMID:16410789	PCS		7/16			P	HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001102	PMID:24749718	PCS		38/40			P	HPO:iea[2009-02-17];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0011506	PMID:24749718	PCS	HP:0003596	17/50			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0000573	PMID:20301292	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0025115	PMID:15970621	PCS		HP:0040284			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001681	PMID:25383264	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0000608	PMID:24749718	PCS		5/40			P	HPO:iea[2009-02-17];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001718	PMID:1600795	PCS		HP:0040284			P	HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0000822	PMID:23935882	PCS		19/67			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0100817	PMID:15970621	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0000007	PMID:16410789	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001635	PMID:23935882	PCS		HP:0040284			P	HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0000505	PMID:16410789	PCS	HP:0003581	7/15			P	HPO:probinson[2009-02-17];HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0025507	PMID:16410789	PCS		12/16			P	HPO:probinson[2020-05-28]
OMIM:264800	Pseudoxanthoma elasticum		HP:0004943	PMID:23968982	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001634	PMID:23968982;PMID:23935882	PCS	HP:0003581	4/99			P	HPO:probinson[2020-06-06];HPO:iea[2009-02-17];HPO:probinson[2020-06-06]
OMIM:264800	Pseudoxanthoma elasticum		HP:0001677	PMID:23935882	PCS		3/67			P	HPO:probinson[2020-05-28];HPO:probinson[2020-06-06]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0001310	PMID:27153400;PMID:28321562;PMID:29379883	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0001272	PMID:29678961	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002066	PMID:27153400;PMID:29379883	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0000020	PMID:27153400	PCS		2/8			P	HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0001251	PMID:27153400;PMID:29678961	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002141	PMID:28321562;PMID:29379883;PMID:29678961	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002061	PMID:27153400;PMID:28321562;PMID:29379883	PCS		11/12			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0003390	PMID:27153400	PCS		2/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0000639	PMID:27153400	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0007340	PMID:27153400;PMID:28321562	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0011462	PMID:27153400;PMID:28321562;PMID:29379883	PCS		11/13			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002936	PMID:27153400	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0006855	PMID:28321562	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0003202	PMID:27153400	PCS		2/8			P	HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0003621	PMID:29379883;PMID:29678961	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002650	PMID:27153400	PCS		1/8			P	HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0003487	PMID:27153400;PMID:28321562;PMID:29678961	PCS		8/10			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0001288	PMID:27153400	PCS		2/8			P	HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0001761	PMID:27153400	PCS		5/8			P	HPO:probinson[2017-06-25];HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002497	PMID:28321562;PMID:29678961	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002395	PMID:27153400;PMID:28321562;PMID:29678961	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0001260	PMID:27153400;PMID:28321562;PMID:29379883;PMID:29678961	PCS		11/13			P	ORCID:0000-0002-0736-9199[2024-05-09];HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002070	PMID:29379883	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0011448	PMID:27153400;PMID:28321562;PMID:29678961	PCS		4/10			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0008081	PMID:27153400	PCS		1/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0034353	PMID:29678961	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0007350	PMID:27153400	PCS		7/8			P	HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0009830	PMID:27153400	PCS		2/8			P	HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0000007	PMID:27153400	PCS					I	HPO:probinson[2017-06-25]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0002505	PMID:29379883;PMID:29678961	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0001258	PMID:27153400	PCS		7/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616907	Spastic paraplegia 76, autosomal recessive		HP:0006986	PMID:28321562;PMID:29379883	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:618094	Deafness, autosomal recessive 110		HP:0003577	PMID:29449721	PCS		2/2			C	HPO:probinson[2023-05-17]
OMIM:618094	Deafness, autosomal recessive 110		HP:0001751	PMID:29449721	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-17]
OMIM:618094	Deafness, autosomal recessive 110		HP:0000407	PMID:29449721	PCS	HP:0003577	2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-17]
OMIM:618094	Deafness, autosomal recessive 110		HP:0000007	PMID:29449721	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-05-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000286	PMID:21218045	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002069	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0004840	OMIM:301040	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001250	PMID:21218045	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0010808	OMIM:301040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0003196	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001252	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0010806	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002020	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0011463	PMID:21218045	PCS		1/1			C	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0012471	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002937	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000316	PMID:21218045	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0009466	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0008897	OMIM:301040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001566	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000158	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002019	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000358	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001249	PMID:21218045	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002751	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000054	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000252	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002673	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002033	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001263	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0011800	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001182	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000407	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001537	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001257	OMIM:301040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000047	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001612	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000369	PMID:21218045	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000049	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000126	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0008947	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000463	PMID:21218045	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001629	OMIM:301040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0011682	OMIM:301040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0008551	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000733	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0030084	OMIM:301040	TAS					P	HPO:skoehler[2014-09-21]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001423	OMIM:301040	IEA					I	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000179	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000699	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0011907	OMIM:301040	TAS					P	HPO:probinson[2012-06-03]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002059	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001762	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002650	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0011903	PMID:21218045	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000272	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0005280	PMID:21218045	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002808	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0001510	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000303	PMID:21218045	PCS		1/1			P	HPO:probinson[2022-08-23]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000028	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0000104	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:301040	Alpha-thalassemia/impaired intellectual development syndrome		HP:0002688	OMIM:301040	IEA					P	HPO:iea[2009-02-17]
OMIM:600803	Gallbladder disease 1		HP:0001396	PMID:11313316	PCS		6/6			P	HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0003155	OMIM:600803	TAS					P	HPO:skoehler[2012-12-30]
OMIM:600803	Gallbladder disease 1		HP:0003581	PMID:11313316	PCS		6/6			C	HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0001395	OMIM:600803	TAS					P	HPO:skoehler[2012-12-30]
OMIM:600803	Gallbladder disease 1		HP:0001081	PMID:11313316	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0001082	OMIM:600803	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600803	Gallbladder disease 1		HP:0011980	PMID:11313316	PCS		6/6			P	HPO:skoehler[2012-12-30];HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0033196	PMID:11313316	PCS		3/3			P	HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0001408	PMID:11313316	PCS		3/3			P	HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0000007	PMID:11313316	PCS					I	HPO:skoehler[2012-12-30];HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0030151	OMIM:600803	TAS					P	HPO:skoehler[2015-01-04]
OMIM:600803	Gallbladder disease 1		HP:0002910	OMIM:600803	TAS					P	HPO:skoehler[2012-12-30]
OMIM:600803	Gallbladder disease 1		HP:0000006	PMID:11313316	PCS					I	HPO:skoehler[2012-12-30];HPO:probinson[2022-08-11]
OMIM:600803	Gallbladder disease 1		HP:0000952	OMIM:600803	TAS		HP:0040283			P	HPO:skoehler[2012-12-30]
OMIM:600803	Gallbladder disease 1		HP:0001733	OMIM:600803	TAS					P	HPO:skoehler[2012-12-30]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0008935	OMIM:614876	TAS					P	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0031956	OMIM:614876	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0001250	OMIM:614876	TAS					P	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0002240	OMIM:614876	TAS					P	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0000162	OMIM:614876	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0001290	OMIM:614876	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0011344	OMIM:614876	TAS					P	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0010655	OMIM:614876	TAS					P	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0001629	PMID:9837814	PCS					P	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0000518	OMIM:614876	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0000007	OMIM:614876	TAS					I	HPO:probinson[2013-01-09]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0008872	OMIM:614876	TAS					P	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0001522	OMIM:614876	TAS					C	HPO:probinson[2013-02-24]
OMIM:614876	Peroxisome biogenesis disorder 8A (Zellweger)		HP:0000952	OMIM:614876	TAS					P	HPO:skoehler[2017-07-13]
OMIM:217150	Contractures, congenital, torticollis, and malignant hyperthermia		HP:0002047	OMIM:217150	IEA					P	HPO:iea[2009-02-17]
OMIM:217150	Contractures, congenital, torticollis, and malignant hyperthermia		HP:0000473	OMIM:217150	IEA					P	HPO:skoehler[2015-12-30]
OMIM:217150	Contractures, congenital, torticollis, and malignant hyperthermia		HP:0000175	OMIM:217150	IEA					P	HPO:iea[2009-02-17]
OMIM:217150	Contractures, congenital, torticollis, and malignant hyperthermia		HP:0000277	OMIM:217150	IEA					P	HPO:iea[2009-02-17]
OMIM:217150	Contractures, congenital, torticollis, and malignant hyperthermia		HP:0000695	OMIM:217150	IEA					P	HPO:iea[2009-02-17]
OMIM:217150	Contractures, congenital, torticollis, and malignant hyperthermia		HP:0000007	OMIM:217150	IEA					I	HPO:iea[2009-02-17]
OMIM:217150	Contractures, congenital, torticollis, and malignant hyperthermia		HP:0002804	OMIM:217150	IEA					P	HPO:iea[2009-02-17]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0003687	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0031956	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0003236	PMID:11805270	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0030237	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0003621	PMID:11805270	PCS		1/1			C	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0001761	OMIM:614321	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0003198	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0008981	OMIM:614321	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0025435	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0003803	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0008954	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0001962	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0000006	PMID:11805270	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0003557	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:614321	Myopathy, distal, Tateyama type		HP:0003722	PMID:11805270	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0003697	OMIM:181405	TAS					P	HPO:probinson[2012-04-11]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0010628	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0003555	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0010307	OMIM:181405	IEA					P	HPO:skoehler[2018-10-08]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0003691	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0001270	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0003391	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0009060	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0009063	OMIM:181405	TAS					P	HPO:probinson[2012-04-11]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0001609	OMIM:181405	IEA					P	HPO:skoehler[2019-09-07]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0003829	OMIM:181405	TAS					I	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0009049	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0002936	OMIM:181405	TAS		HP:0040283			P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0003307	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0030084	OMIM:181405	TAS					P	HPO:skoehler[2014-09-21]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0006897	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0001840	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0008955	OMIM:181405	TAS					P	HPO:probinson[2012-04-11]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0001265	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0000473	OMIM:181405	TAS					P	HPO:skoehler[2013-11-28]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0002136	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0001385	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0001762	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0002650	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0011727	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0001284	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0002093	OMIM:181405	IEA					P	HPO:skoehler[2018-10-08]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0002808	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0009113	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0007178	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0200055	OMIM:181405	TAS					P	HPO:skoehler[2013-06-23]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0000006	OMIM:181405	TAS					I	HPO:probinson[2012-04-11]
OMIM:181405	Scapuloperoneal spinal muscular atrophy		HP:0003634	OMIM:181405	TAS					P	HPO:probinson[2012-04-11]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0002069	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0001272	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0001252	PMID:33880529	PCS		4/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0003593	PMID:33880529	PCS		1/6			C	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0033725	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0012650	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0011463	PMID:33880529	PCS		2/6			C	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0000817	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0020221	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0001522	PMID:33880529	PCS		1/6			C	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0003623	PMID:33880529	PCS		1/6			C	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0003621	PMID:33880529	PCS		3/6			C	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0002059	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0001344	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0001263	PMID:33880529	PCS		5/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0005484	PMID:33880529	PCS		2/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0010851	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0010535	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0032867	PMID:33880529	PCS		2/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0007074	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0003819	PMID:33880529	PCS		1/6			C	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0007334	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0007359	PMID:33880529	PCS		4/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0007018	PMID:33880529	PCS		1/6			P	HPO:probinson[2022-02-26]
OMIM:619605	Developmental and epileptic encephalopathy 98		HP:0000006	PMID:33880529	PCS					I	HPO:probinson[2022-02-26]
OMIM:620084	Spermatogenic failure 76		HP:0033393	PMID:34348960	PCS		1/2			P	HPO:probinson[2022-11-24]
OMIM:620084	Spermatogenic failure 76		HP:0003251	PMID:34348960	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:620084	Spermatogenic failure 76		HP:0011462	PMID:34348960	PCS		2/2			C	HPO:probinson[2022-11-24]
OMIM:620084	Spermatogenic failure 76		HP:0000007	PMID:34348960	PCS					I	HPO:probinson[2022-11-24]
OMIM:620084	Spermatogenic failure 76		HP:0012207	PMID:34348960	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:620084	Spermatogenic failure 76		HP:0000798	PMID:34348960	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:620084	Spermatogenic failure 76		HP:0032558	PMID:34348960	PCS		1/2			P	HPO:probinson[2022-11-24];HPO:probinson[2022-11-24]
OMIM:620084	Spermatogenic failure 76		HP:0032559	PMID:34348960	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:147250	Solitary median maxillary central incisor		HP:0000252	OMIM:147250;PMID:11471164	PCS		8/24			P	HPO:iea[2009-10-30];HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0009914	PMID:12503095	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0025011	OMIM:147250	IEA					P	HPO:skoehler[2018-10-08]
OMIM:147250	Solitary median maxillary central incisor		HP:0000453	PMID:11471164	PCS		8/14			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0004322	PMID:11471164	PCS		7/14			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0001360	OMIM:147250	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0010644	PMID:11471164	PCS		9/14			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0001739	PMID:11471164	PCS		1/14			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0002708	PMID:11471164	PCS		14/14			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0000528	PMID:12503095	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0003828	OMIM:147250	PCS					M	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0100789	OMIM:147250	TAS					P	HPO:skoehler[2013-06-12]
OMIM:147250	Solitary median maxillary central incisor		HP:0002916	PMID:11471164	PCS		2/14			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0001328	PMID:11471164	PCS		5/14			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0000601	PMID:11471164	PCS		8/14			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0000458	OMIM:147250	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0000568	PMID:12503095	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0000824	PMID:925821	PCS		5/7			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0000006	OMIM:147250	PCS					I	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0006315	OMIM:147250	PCS		100%			P	HPO:iea[2009-02-17]
OMIM:147250	Solitary median maxillary central incisor		HP:0000204	PMID:11471164	PCS		1/14			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0000589	PMID:12503095	PCS		HP:0040283			P	HPO:iea[2009-11-30]
OMIM:147250	Solitary median maxillary central incisor		HP:0000830	PMID:11471164	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002982	PMID:29213174	PCS		1/1			P	HPO:probinson[2012-05-01]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002980	PMID:9768646	PCS		1/1			P	HPO:probinson[2012-05-01];HPO:probinson[2022-04-28]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0004322	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0003155	PMID:29213174	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0004363	PMID:29213174;PMID:9768646	PCS		1/2			P	HPO:probinson[2024-02-22];HPO:skoehler[2014-11-26];HPO:probinson[2022-04-28]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0003593	PMID:9768646	PCS		1/1			C	HPO:probinson[2022-04-28]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0010502	OMIM:307800	TAS					P	HPO:probinson[2012-05-01]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002979	PMID:29213174	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0000117	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0006432	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002515	PMID:29213174	PCS		1/1			P	HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002857	PMID:9768646	PCS		1/1			P	HPO:probinson[2022-04-28]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002758	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0004912	PMID:29213174	PCS		1/1			P	HPO:probinson[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0001423	PMID:7550339	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0008117	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0000897	PMID:29213174	PCS		1/1			P	HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002653	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0031936	PMID:29213174	PCS		1/1			P	HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0003025	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0003165	OMIM:307800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002176	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0004273	PMID:29213174	PCS		1/1			P	HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002194	PMID:29213174	PCS		1/1			P	HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002829	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0006285	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0008144	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002748	PMID:29213174;PMID:9768646	PCS		2/2			P	HPO:probinson[2022-04-28];HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002749	OMIM:307800	TAS					P	HPO:probinson[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002007	PMID:29213174	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0001433	PMID:29213174	PCS		1/1			P	HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0000124	OMIM:307800	TAS					P	HPO:probinson[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0003416	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002148	PMID:29213174;PMID:9768646	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-04-28];HPO:probinson[2024-02-22]
OMIM:307800	Hypophosphatemic rickets, X-linked dominant		HP:0002644	OMIM:307800	IEA					P	HPO:iea[2009-02-17]
OMIM:613328	Roifman-Chitayat syndrome		HP:0000431	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0002123	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0000086	OMIM:613328	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613328	Roifman-Chitayat syndrome		HP:0001263	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0000470	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0010049	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0002090	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0005280	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0010579	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0100660	OMIM:613328	IEA					P	HPO:skoehler[2019-09-07]
OMIM:613328	Roifman-Chitayat syndrome		HP:0010743	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0010282	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0009891	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0000938	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0000316	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0001537	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0001999	OMIM:613328	IEA					P	HPO:skoehler[2015-01-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0000007	OMIM:613328	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0002119	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613328	Roifman-Chitayat syndrome		HP:0000648	OMIM:613328	IEA					P	HPO:skoehler[2015-12-30]
OMIM:613328	Roifman-Chitayat syndrome		HP:0007678	OMIM:613328	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613328	Roifman-Chitayat syndrome		HP:0001369	OMIM:613328	IEA					P	HPO:skoehler[2010-06-19]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0011939	PMID:20618352;PMID:33688495	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0003577	PMID:20618352;PMID:33688495;PMID:26078953	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0010946	PMID:20618352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000662	PMID:20618352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000041	PMID:20618352;PMID:33688495	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0012745	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0012622	PMID:20618352;PMID:26078953	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0031624	PMID:20618352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000819	PMID:20618352;PMID:33688495;PMID:23829372;PMID:26078953	PCS		13/14			P	ORCID:0000-0002-0736-9199[2024-04-24];HP:probinson[2019-02-03]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000319	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0032285	PMID:20618352;PMID:26078953	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001647	OMIM:615981	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000414	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000678	PMID:26078953	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000752	PMID:33688495	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000510	PMID:20618352;PMID:33688495;PMID:23829372;PMID:26078953	PCS		14/14			P	HPO:skoehler[2014-11-26];HP:probinson[2019-02-03];ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000135	PMID:33688495	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000311	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001249	PMID:20618352;PMID:11285252;PMID:33688495;PMID:26078953	PCS		14/14			P	HPO:skoehler[2014-11-26];HP:probinson[2019-02-03];ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001644	PMID:7802002	PCS		HP:0040283			P	HPO:skoehler[2014-11-26];HP:probinson[2019-02-03]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000494	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000054	PMID:33688495	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000233	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001162	PMID:20618352;PMID:11285252;PMID:33688495;PMID:26078953	PCS		14/14			P	HPO:skoehler[2014-11-26];HP:probinson[2019-02-03];ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000490	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001263	PMID:20618352;PMID:16823392	PCS		3/3			P	HPO:skoehler[2014-11-26];HP:probinson[2019-02-03];ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0003241	OMIM:615981	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000470	PMID:33688495;PMID:26078953	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0005280	PMID:33688495;PMID:26078953	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001959	PMID:20618352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000822	PMID:20618352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000007	PMID:11285252	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-02-03]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000546	PMID:23829372	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0007994	PMID:20618352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001511	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000103	PMID:20618352	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001830	PMID:20618352;PMID:11285252;PMID:33688495;PMID:26078953	PCS		13/14			P	ORCID:0000-0002-0736-9199[2024-04-24];HP:probinson[2019-02-03]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001631	OMIM:615981	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000047	PMID:20618352;PMID:33688495	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0000003	PMID:20618352;PMID:33688495;PMID:26078953	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615981	Bardet-Biedl syndrome 2		HP:0001513	PMID:20618352;PMID:11285252;PMID:33688495;PMID:26078953	PCS		14/14			P	HPO:skoehler[2014-11-26];HP:probinson[2019-02-03];ORCID:0000-0002-0736-9199[2024-04-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0003774	PMID:24026985	PCS	HP:0003596	1/1			P	HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0001156	PMID:24026985	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0000518	PMID:24026985	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0000083	PMID:24026985	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0000007	PMID:24026985	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0000510	PMID:24026985	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0001513	PMID:24026985	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0000556	PMID:24026985	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-24]
OMIM:615995	Bardet-Biedl syndrome 18		HP:0001249	PMID:24026985	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001297	PMID:30792199	PCS		25/120			P	HPO:probinson[2021-02-25]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001289	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001981	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0005575	OMIM:274150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0002098	OMIM:274150	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0002151	OMIM:274150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0000093	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0012211	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001937	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0002907	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001658	PMID:30792199	PCS		5/120			P	HPO:probinson[2021-02-25]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0000007	PMID:11586351	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001945	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001923	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0002326	PMID:30792199	PCS		12/120			P	HPO:probinson[2021-02-25]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001873	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0003259	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0003138	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0000952	PMID:30792199	PCS		59/120			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-25]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0006579	OMIM:274150	TAS					P	HPO:skoehler[2013-06-03]
OMIM:274150	Thrombotic thrombocytopenic purpura, hereditary		HP:0001337	OMIM:274150	IEA					P	HPO:iea[2009-02-17]
OMIM:619177	Spermatogenic failure 51		HP:0033393	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0032560	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0032561	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0000007	PMID:32161152	PCS					I	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0012207	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0025437	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0033525	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0000798	PMID:32161152	PCS		3/6			P	HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0032558	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30]
OMIM:619177	Spermatogenic failure 51		HP:0032559	PMID:32161152	PCS		6/6			P	HPO:probinson[2021-04-30]
OMIM:619611	Interstitial lung disease 1		HP:0033638	PMID:30854216	PCS		1/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0030830	PMID:30854216	PCS		3/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0003596	PMID:30854216	PCS		2/4			C	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0003584	PMID:30854216	PCS		1/4			C	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0025179	PMID:30854216	PCS		3/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0002094	PMID:30854216	PCS		4/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0012735	PMID:30854216	PCS		2/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0031950	PMID:30854216	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0002091	PMID:30854216	PCS		2/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0030879	PMID:30854216	PCS		3/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0032987	PMID:30854216	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0032977	PMID:30854216	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0045051	PMID:30854216	PCS		2/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0011462	PMID:30854216	PCS		1/4			C	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0033584	PMID:30854216	PCS		1/2			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0001217	PMID:30854216	PCS		2/4			P	HPO:probinson[2022-02-27]
OMIM:619611	Interstitial lung disease 1		HP:0000006	PMID:26792177	PCS					I	HPO:probinson[2022-02-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0003235	OMIM:222470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0002224	OMIM:222470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001894	PMID:20176027	PCS		4/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0004322	OMIM:222470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000160	OMIM:222470	TAS					P	HPO:skoehler[2012-11-20]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0003073	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000957	PMID:20176027	PCS		2/12			P	HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0011220	PMID:28292286	PCS		20/20			P	HPO:skoehler[2009-02-17];HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000316	PMID:28292286;PMID:20176027	PCS		32/32			P	HPO:probinson[2022-08-08];HPO:iea[2009-02-17];HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001642	PMID:20176027	PCS		1/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000952	OMIM:222470	TAS					P	HPO:skoehler[2012-11-20]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000494	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0005743	PMID:20176027	PCS		1/12			P	HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0012023	PMID:7073301	PCS		2/2			P	HPO:skoehler[2012-11-20];HPO:probinson[2024-03-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0012024	PMID:7073301	PCS		0/2			P	HPO:skoehler[2012-11-20];HPO:probinson[2024-03-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0009891	OMIM:222470	TAS					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000007	PMID:28292286	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0006267	OMIM:222470	TAS					P	HPO:skoehler[2012-10-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001659	PMID:20176027	PCS		2/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000520	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000047	PMID:28292286	PCS		3/20			P	HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0007513	PMID:20176027	PCS		1/12			P	HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000369	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001732	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000445	OMIM:222470	TAS					P	HPO:skoehler[2012-11-20]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001396	OMIM:222470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001399	OMIM:222470	TAS					P	HPO:skoehler[2012-11-20]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000343	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000463	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001194	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0003452	OMIM:222470	IEA	HP:0003577				P	HPO:skoehler[2018-10-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001395	PMID:28292286;PMID:20176027	PCS		14/27			P	HPO:probinson[2022-08-08];HPO:skoehler[2009-02-17];HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0002041	PMID:20176027	PCS		12/12			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001394	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0002240	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0011877	PMID:20176027	PCS		5/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0008070	OMIM:222470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0100543	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001508	PMID:20176027	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001629	PMID:20176027	PCS		1/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0008551	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000337	PMID:20176027	PCS		12/12			P	HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0009886	PMID:28292286;PMID:20176027	PCS		22/22			P	HPO:probinson[2022-08-08];HPO:skoehler[2012-10-17];HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000457	OMIM:222470	TAS					P	HPO:skoehler[2012-11-20]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0004734	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001744	PMID:20176027	PCS		2/9			P	HPO:probinson[2022-08-08];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0002212	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000154	OMIM:222470	TAS					P	HPO:skoehler[2012-11-20]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0002213	OMIM:222470	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001561	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0004313	PMID:20176027	PCS		11/12			P	HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0002299	OMIM:222470	TAS					P	HPO:skoehler[2012-10-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0000193	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0012758	PMID:28292286	PCS		10/16			P	HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0011031	OMIM:222470	TAS					P	HPO:skoehler[2012-11-20]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001518	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0011473	PMID:28292286;PMID:20176027	PCS		32/32			P	HPO:probinson[2022-08-08];HPO:skoehler[2012-10-17];HP:probinson[2019-05-27]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001636	PMID:20176027	PCS	HP:0030674	1/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-08]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0002007	OMIM:222470	IEA					P	HPO:iea[2009-02-17]
OMIM:222470	Trichohepatoenteric syndrome 1		HP:0001511	PMID:28292286;PMID:20176027	PCS	HP:0011461	33/35			P	HPO:probinson[2022-08-08];HPO:iea[2009-02-17];HP:probinson[2019-05-27]
OMIM:610153	Deafness, autosomal recessive 49		HP:0003577	PMID:17186462	PCS					C	HPO:probinson[2022-05-26]
OMIM:610153	Deafness, autosomal recessive 49		HP:0000007	PMID:17186462	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-26]
OMIM:610153	Deafness, autosomal recessive 49		HP:0000399	PMID:17186462	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-26]
OMIM:603649	Cone-rod dystrophy 7		HP:0012045	PMID:9634506	PCS		0/9			P	HPO:probinson[2013-02-20];HPO:probinson[2021-05-29];HPO:probinson[2024-03-10]
OMIM:603649	Cone-rod dystrophy 7		HP:0000551	PMID:9634506	PCS	HP:0011462				P	HPO:probinson[2013-02-20];HPO:probinson[2021-05-29]
OMIM:603649	Cone-rod dystrophy 7		HP:0000505	PMID:9634506	PCS	HP:0003581				P	HPO:probinson[2013-02-20];HPO:probinson[2021-05-29]
OMIM:603649	Cone-rod dystrophy 7		HP:0000548	PMID:9634506	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-05-29]
OMIM:603649	Cone-rod dystrophy 7		HP:0007401	PMID:9634506	PCS					P	HPO:probinson[2021-05-29]
OMIM:603649	Cone-rod dystrophy 7		HP:0011504	PMID:9634506	PCS					P	HPO:probinson[2013-02-20];HPO:probinson[2021-05-29]
OMIM:603649	Cone-rod dystrophy 7		HP:0000006	PMID:12659814	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-21]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0012385	OMIM:614335	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0001762	OMIM:614335	IEA		9/12			P	HPO:skoehler[2013-01-09]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0001838	OMIM:614335	IEA		3/12			P	HPO:skoehler[2013-01-09]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0005684	OMIM:614335	IEA		HP:0040280			P	HPO:skoehler[2013-01-09]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0009473	OMIM:614335	IEA		5/12			P	HPO:skoehler[2013-01-09]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0008366	OMIM:614335	IEA		HP:0040281			P	HPO:skoehler[2013-01-09]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0002804	OMIM:614335	IEA					P	HPO:skoehler[2015-01-19]
OMIM:614335	Arthrogryposis, distal, type 1B		HP:0000006	OMIM:614335	TAS					I	HPO:skoehler[2017-07-13]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0004325	OMIM:270450	IEA					P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0003510	PMID:14657428	PCS		2/4			P	HPO:probinson[2023-03-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001773	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000486	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0004322	OMIM:270450	IEA					P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000160	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0009381	PMID:14657428	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000319	OMIM:270450	TAS					P	HPO:probinson[2012-05-01]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000558	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0009466	OMIM:270450	IEA					P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000713	OMIM:270450	IEA		1/4			P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000278	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001249	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0002553	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000252	OMIM:270450	IEA		1/4			P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0030269	OMIM:270450	TAS					P	HPO:probinson[2015-01-31]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000574	PMID:14657428	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0002750	OMIM:270450	IEA		2/4			P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0002079	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000490	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001263	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000767	OMIM:270450	IEA		1/4			P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000007	OMIM:270450	IEA					I	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0003758	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001852	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000006	PMID:14657428	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000369	OMIM:270450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000325	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001655	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0003577	PMID:14657428;OMIM:270450	PCS		14/14			C	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000582	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000343	OMIM:270450	TAS					P	HPO:probinson[2012-05-01]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001270	OMIM:270450	IEA		1/4			P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000819	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001629	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000739	OMIM:270450	TAS		1/4			P	HPO:probinson[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001547	OMIM:270450	IEA					P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0009125	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000219	OMIM:270450	IEA					P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0030084	OMIM:270450	TAS		1/4			P	HPO:skoehler[2014-09-21]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000218	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0006610	OMIM:270450	IEA		1/4			P	HPO:skoehler[2019-04-18]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001620	OMIM:270450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000750	OMIM:270450	IEA		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000431	OMIM:270450	IEA		1/4			P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001999	OMIM:270450	IEA					P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0002209	OMIM:270450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001956	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001511	OMIM:270450	IEA		4/4			P	HPO:iea[2009-02-17]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0200055	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000664	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001631	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0001510	PMID:14657428	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000465	OMIM:270450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:270450	Insulin-Like growth factor I, resistance to		HP:0000347	OMIM:270450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:207800	Argininemia		HP:0001396	PMID:2913054	PCS		1/1			P	HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0001250	OMIM:207800	IEA					P	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0001272	PMID:32606543	PCS		1/1			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0002240	PMID:2913054	PCS		1/1			P	HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0002064	PMID:32606543	PCS		1/1			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:4000203	OMIM:207800	TAS					P	HPO:probinson[2024-01-06]
OMIM:207800	Argininemia		HP:0000737	OMIM:207800	IEA					P	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0011463	PMID:32606543	PCS		1/1			C	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0001987	PMID:2913054;OMIM:207800;PMID:32606543	PCS		12/12			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04];HPO:probinson[2020-09-04];HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0008897	OMIM:207800	IEA					P	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0000752	OMIM:207800	IEA					P	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0002359	PMID:32606543	PCS		1/1			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0001249	PMID:29726057	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0002478	OMIM:207800	IEA					P	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0002313	PMID:29726057	PCS					P	HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0008339	OMIM:207800	IEA					P	HPO:probinson[2012-03-25]
OMIM:207800	Argininemia		HP:0002039	OMIM:207800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:207800	Argininemia		HP:0003623	PMID:2913054	PCS		1/1			C	HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0002013	OMIM:207800	IEA					P	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0002572	PMID:32606543	PCS		1/1			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0001263	OMIM:207800	IEA					P	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0500153	PMID:2913054;PMID:32606543;PMID:29726057	PCS		12/12			P	HPO:probinson[2020-09-04];HPO:probinson[2020-09-04];HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0006580	PMID:2913054	PCS		1/1			P	HPO:probinson[2020-09-04]
OMIM:207800	Argininemia		HP:0000007	OMIM:207800	IEA					I	HPO:iea[2009-02-17]
OMIM:207800	Argininemia		HP:0003218	OMIM:207800	PCS					P	HPO:probinson[2012-03-25]
OMIM:207800	Argininemia		HP:0001413	PMID:2913054	PCS		1/1			P	HPO:probinson[2020-09-04]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002663	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003015	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002983	PMID:28263186	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001591	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003099	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0030674	PMID:28263186	PCS		7/7			C	HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003375	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002240	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003270	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0100864	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0008450	OMIM:602557	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001609	PMID:28263186	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002938	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0008873	PMID:28263186	PCS		7/7			P	HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002812	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002953	PMID:28263186	PCS					P	HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0000773	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001744	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0008417	OMIM:602557	TAS	HP:0003593				P	HPO:skoehler[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0009826	PMID:28263186	PCS	HP:0030674	7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0000233	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002650	PMID:28263186	PCS					P	HPO:probinson[2022-10-23];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002970	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003025	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002651	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001382	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0000470	PMID:28263186	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0008463	OMIM:602557	IEA					P	HPO:iea[2009-02-17]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0000926	PMID:28263186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:602557	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0000007	PMID:28263186	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-23]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000175	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000013	OMIM:601076	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000772	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0004322	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000122	OMIM:601076	IEA					P	HPO:skoehler[2015-12-30]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000086	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0002350	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000925	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000813	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000912	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000405	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0003745	OMIM:601076	IEA					I	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000204	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000347	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000027	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000104	OMIM:601076	IEA					P	HPO:skoehler[2010-06-18]
OMIM:601076	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracicsomite anomalies		HP:0000324	OMIM:601076	IEA					P	HPO:iea[2009-02-17]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0002069	PMID:33420346	PCS		5/8			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0000750	PMID:33420346	PCS		8/8			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0002540	PMID:33420346	PCS		5/6			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0004322	PMID:33420346	PCS		3/6			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0000729	PMID:33420346	PCS		2/6			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0000718	PMID:33420346	PCS		2/6			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0001252	PMID:33420346	PCS		7/8			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0002061	PMID:33420346	PCS		5/8			P	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0000007	PMID:33420346	PCS					I	HPO:probinson[2022-02-02]
OMIM:619639	Neurodevelopmental disorder with hypotonia and gross motor and seech delay		HP:0007018	PMID:33420346	PCS		2/6			P	HPO:probinson[2022-02-02]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0011273	PMID:16783379	PCS		8/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0004445	PMID:16783379	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0004312	OMIM:300835	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0012135	OMIM:300835	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0003540	PMID:16783379	PCS		2/2			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0001419	PMID:16783379	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0003593	PMID:16783379	PCS					C	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0005528	PMID:16783379	PCS		5/8			P	HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0001972	PMID:16783379	PCS		8/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0001873	PMID:16783379	PCS		0/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0001875	PMID:16783379	PCS		6/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:300835	Anemia, X-linked, with or without neutropenia and/or platelet abnormalities		HP:0004447	PMID:16783379	PCS		6/8			P	HPO:skoehler[2012-10-14];HPO:probinson[2023-02-04]
OMIM:606719	Melanoma-Pancreatic cancer syndrome		HP:0002861	OMIM:606719	IEA					P	HPO:skoehler[2010-06-19]
OMIM:606719	Melanoma-Pancreatic cancer syndrome		HP:0006725	OMIM:606719	TAS					P	HPO:skoehler[2010-06-19]
OMIM:606719	Melanoma-Pancreatic cancer syndrome		HP:0002860	OMIM:606719	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606719	Melanoma-Pancreatic cancer syndrome		HP:0012142	OMIM:606719	TAS					P	HPO:probinson[2012-09-16]
OMIM:606719	Melanoma-Pancreatic cancer syndrome		HP:0012182	OMIM:606719	TAS					P	HPO:skoehler[2013-02-25]
OMIM:606719	Melanoma-Pancreatic cancer syndrome		HP:0000006	OMIM:606719	IEA					I	HPO:skoehler[2010-06-19]
OMIM:606719	Melanoma-Pancreatic cancer syndrome		HP:0100242	OMIM:606719	TAS					P	HPO:skoehler[2012-08-01]
OMIM:106230	Aniridia, microcornea, and spontaneously reabsorbed cataract		HP:0000518	OMIM:106230	IEA					P	HPO:skoehler[2018-10-08]
OMIM:106230	Aniridia, microcornea, and spontaneously reabsorbed cataract		HP:0000482	OMIM:106230	TAS					P	HPO:probinson[2009-02-17]
OMIM:106230	Aniridia, microcornea, and spontaneously reabsorbed cataract		HP:0000526	OMIM:106230	TAS					P	HPO:probinson[2009-02-17]
OMIM:106230	Aniridia, microcornea, and spontaneously reabsorbed cataract		HP:0000006	OMIM:106230	TAS					I	HPO:probinson[2009-02-17]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001133	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001036	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001310	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001251	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0003593	PMID:29496980	PCS		2/2			C	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001270	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000639	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000958	PMID:29496980	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000217	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000613	PMID:29496980	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0007663	OMIM:618527	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000956	OMIM:618527	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0003429	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001348	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001249	PMID:29496980	PCS		0/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000011	OMIM:618527	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001583	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0003487	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001260	PMID:29496980	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0025092	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0008064	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000407	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001258	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000543	PMID:29496980	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001257	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0001337	PMID:29496980	PCS		1/2			P	HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000006	PMID:29496980	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-06-20]
OMIM:618527	Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features		HP:0000962	PMID:29496980	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0001133	OMIM:520000	TAS		20/20			P	HPO:probinson[2015-07-20];HPO:iea[2009-02-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0001751	OMIM:520000	IEA					P	HPO:iea[2009-02-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0002321	OMIM:520000	TAS					P	HPO:skoehler[2014-01-28]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0001250	OMIM:520000	IEA					P	HPO:iea[2009-02-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0001260	OMIM:520000	IEA					P	HPO:iea[2009-02-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0000580	PMID:8094200	PCS					P	HPO:probinson[2017-12-22]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0003074	OMIM:520000	IEA					P	HPO:iea[2009-02-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0000407	OMIM:520000	TAS					P	HPO:probinson[2013-12-16]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0000508	OMIM:520000	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0001427	OMIM:520000	TAS					I	HPO:skoehler[2012-10-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0000546	OMIM:520000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0001638	OMIM:520000	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0002317	OMIM:520000	IEA					P	HPO:iea[2009-02-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0005978	OMIM:520000	IEA					P	HPO:iea[2009-02-17]
OMIM:520000	Diabetes and deafness, maternally inherited		HP:0000544	OMIM:520000	IEA					P	HPO:iea[2009-02-17]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002465	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0003577	PMID:20818383	PCS		1/1			C	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002540	PMID:20858599	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001250	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001272	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002063	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001252	PMID:20818383	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001252	PMID:20858599	PCS	HP:0003623	1/1			P	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0012448	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0000737	PMID:20858599	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0100704	PMID:20858599	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001943	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002119	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0003623	PMID:20858599	PCS		1/1			C	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0003128	PMID:20818383	PCS	HP:0003577	1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002650	OMIM:618241	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001344	PMID:20818383	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001288	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0011968	OMIM:618241	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001263	PMID:20858599	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0005484	PMID:20858599	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002093	OMIM:618241	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0011923	PMID:20818383;PMID:20858599	PCS		2/2			P	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001639	PMID:20858599	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0000007	PMID:20818383	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0000648	OMIM:618241	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002505	PMID:20818383	PCS	HP:0003621	1/1			P	HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0002305	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-06]
OMIM:618241	Mitochondrial complex I deficiency, nuclear type 19		HP:0001336	OMIM:618241	IEA					P	HPO:skoehler[2019-02-15]
OMIM:607361	Meckel syndrome 3		HP:0000175	OMIM:607361	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:607361	Meckel syndrome 3		HP:0001162	OMIM:607361	TAS					P	HPO:skoehler[2015-04-26]
OMIM:607361	Meckel syndrome 3		HP:0002085	PMID:17377820	PCS		8/12			P	HPO:probinson[2021-02-14]
OMIM:607361	Meckel syndrome 3		HP:0001395	OMIM:607361	TAS					P	HPO:skoehler[2015-04-26]
OMIM:607361	Meckel syndrome 3		HP:0002240	PMID:17377820	PCS		2/5			P	HPO:probinson[2021-02-14]
OMIM:607361	Meckel syndrome 3		HP:0010442	OMIM:607361	TAS					P	HPO:probinson[2013-02-23]
OMIM:607361	Meckel syndrome 3		HP:0001408	OMIM:607361	TAS					P	HPO:skoehler[2015-04-26]
OMIM:607361	Meckel syndrome 3		HP:0006563	PMID:17377820	PCS		4/5			P	HPO:probinson[2021-02-14]
OMIM:607361	Meckel syndrome 3		HP:0000238	OMIM:607361	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:607361	Meckel syndrome 3		HP:0001305	PMID:17377820	PCS		1/12			P	HPO:skoehler[2015-04-26];HPO:probinson[2021-02-14]
OMIM:607361	Meckel syndrome 3		HP:0000007	PMID:17377820	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2021-02-14]
OMIM:607361	Meckel syndrome 3		HP:0001830	PMID:17377820	PCS		1/12			P	HPO:probinson[2021-02-14]
OMIM:607361	Meckel syndrome 3		HP:0000003	PMID:17377820	PCS		12/12			P	HPO:probinson[2013-08-11];HPO:probinson[2021-02-14]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0000176	OMIM:192445	IEA					P	HPO:iea[2009-02-17]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0000494	OMIM:192445	IEA					P	HPO:iea[2009-02-17]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0009087	OMIM:192445	IEA					P	HPO:iea[2009-02-17]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0010185	OMIM:192445	IEA					P	HPO:iea[2009-02-17]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0006682	OMIM:192445	IEA					P	HPO:iea[2009-02-17]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0001649	OMIM:192445	IEA					P	HPO:skoehler[2010-06-20]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0000201	OMIM:192445	IEA					P	HPO:iea[2009-02-17]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0001279	OMIM:192445	TAS					P	HPO:probinson[2009-02-17]
OMIM:192445	Ventricular extrasystoles with syncope, perodactyly, and Robin sequence		HP:0000006	OMIM:192445	IEA					I	HPO:iea[2009-02-17]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002069	PMID:27164707	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002465	OMIM:617166	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002521	PMID:27164707	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002540	OMIM:617166	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0001272	PMID:27164707	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0001252	PMID:27164707	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0001251	PMID:27164707	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0003593	PMID:27164707	PCS		1/2			C	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0010841	PMID:27164707	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0100704	PMID:27164707	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0012450	OMIM:617166	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0000713	PMID:27164707	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0007843	PMID:27164707	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0003623	PMID:27164707	PCS		1/2			C	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0008936	PMID:27164707	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0001344	PMID:27164707	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002353	PMID:27164707	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002133	PMID:27164707	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002376	PMID:27164707	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0001288	OMIM:617166	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0011968	PMID:27164707	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0005484	PMID:27164707	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0002070	PMID:27164707	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0032792	PMID:27164707	PCS		2/2			P	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0200134	PMID:27164707	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0000543	PMID:27164707	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0007359	PMID:27164707	PCS		1/2			P	HPO:probinson[2023-03-04]
OMIM:617166	Developmental and epileptic encephalopathy 47		HP:0000006	PMID:27164707	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-04]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0001891	PMID:25168382	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0003676	PMID:25168382	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0001399	PMID:25168382	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0025196	PMID:25168382	PCS		1/1			P	HPO:probinson[2021-02-10];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0001395	PMID:25168382	PCS		1/1			P	HPO:probinson[2017-05-29];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0002240	PMID:25168382	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0003593	PMID:25168382	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0012202	PMID:25168382	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0006580	PMID:25168382	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0001409	PMID:25168382	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0002904	PMID:25168382	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0000007	PMID:25168382	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0002910	PMID:25168382	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0000952	PMID:25168382	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0001744	PMID:25168382	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2021-02-10]
OMIM:616278	Bile acid synthesis defect, congenital, 5		HP:0003645	PMID:25168382	PCS		1/1			P	HPO:probinson[2021-02-10]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0001320	PMID:23246003	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0003577	PMID:23246003	PCS		3/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0000750	PMID:23246003	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0002365	PMID:23246003	PCS		2/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0032409	PMID:23246003	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0002198	PMID:23246003	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0001263	PMID:23246003	PCS		3/3		HP:0012828	P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0025102	PMID:23246003	PCS		3/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0001251	PMID:23246003	PCS		1/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0033725	PMID:23246003	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0032471	PMID:23246003	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0011451	PMID:23246003	PCS		3/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0002539	PMID:23246003	PCS		1/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0000568	PMID:23246003	PCS		1/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0001338	PMID:23246003	PCS		2/3			P	HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0007973	PMID:23246003	PCS		1/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-10-24]
OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		HP:0000006	PMID:23246003	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-24]
OMIM:424500	GONADOBLASTOMA		HP:0000150	OMIM:424500	IEA					P	HPO:iea[2009-02-17]
OMIM:424500	GONADOBLASTOMA		HP:0001450	OMIM:424500	IEA					I	HPO:iea[2009-02-17]
OMIM:424500	GONADOBLASTOMA		HP:0001939	OMIM:424500	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0000252	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0000365	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0000420	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0004322	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0001263	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0003196	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0005280	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0010655	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0008064	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0000518	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0000925	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0001419	OMIM:302950	IEA					I	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0009882	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0000458	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:302950	Chondrodysplasia punctata 1, X-linked recessive		HP:0000135	OMIM:302950	IEA					P	HPO:iea[2009-02-17]
OMIM:146600	Ichthyosis hystrix gravior		HP:0008066	PMID:27212473	PCS		0/3			P	HPO:probinson[2023-03-25]
OMIM:146600	Ichthyosis hystrix gravior		HP:0003593	PMID:27212473	PCS		3/3			C	HPO:probinson[2023-03-25]
OMIM:146600	Ichthyosis hystrix gravior		HP:0025080	PMID:27212473	PCS		2/2			P	HPO:probinson[2023-03-25]
OMIM:146600	Ichthyosis hystrix gravior		HP:0000006	PMID:27212473	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:146600	Ichthyosis hystrix gravior		HP:0000962	PMID:27212473	PCS		3/3			P	HPO:probinson[2023-03-25]
OMIM:618533	Deafness, autosomal dominant 37		HP:0000407	PMID:30245514	PCS	HP:0003593				P	HPO:probinson[2020-05-15]
OMIM:618533	Deafness, autosomal dominant 37		HP:0000006	PMID:30245514	PCS					I	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0002069	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0002465	PMID:28288114	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0002384	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0002121	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001252	PMID:28288114	IEA		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0003593	PMID:28288114	PCS		1/5			C	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0032794	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001270	PMID:21076407	PCS		1/1			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0011463	PMID:28288114	PCS		2/5			C	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0000739	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0000733	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0000752	PMID:28288114	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001763	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001642	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001249	PMID:28288114	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0003623	PMID:28288114	PCS		1/5			C	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001166	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0003621	PMID:28288114	PCS		1/5			C	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0000750	PMID:21076407;PMID:28288114	PCS		2/6			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0030148	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0002650	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0002376	PMID:28288114	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0030223	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001263	PMID:21076407;PMID:28288114	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12];HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0002072	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0100021	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0100023	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0000729	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001998	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0000988	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001533	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0007018	PMID:28288114	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0000006	PMID:21076407	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-12]
OMIM:617600	Intellectual developmental disorder, autosomal dominant 45		HP:0001336	PMID:28288114	PCS		1/5			P	HPO:probinson[2022-06-12]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0005326	PMID:32286682	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0003577	PMID:32286682	PCS		2/2			C	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000486	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000574	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0005565	PMID:32286682	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0001250	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000490	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0001263	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0001251	PMID:32286682	PCS		0/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0011451	PMID:32286682	PCS	HP:0003577	2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0004719	PMID:32286682	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000712	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000007	PMID:32286682	PCS					I	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000348	PMID:32286682	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0012081	PMID:32286682	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000307	PMID:32286682	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0000752	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0001249	PMID:32286682	PCS		2/2			P	HPO:probinson[2022-10-02]
OMIM:620047	Microcephaly 29, primary, autosomal recessive		HP:0009879	PMID:32286682	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:180900	Rutherfurd syndrome		HP:0007759	OMIM:180900	IEA					P	HPO:iea[2009-02-17]
OMIM:180900	Rutherfurd syndrome		HP:0000680	OMIM:180900	IEA					P	HPO:iea[2009-02-17]
OMIM:180900	Rutherfurd syndrome		HP:0001131	OMIM:180900	IEA					P	HPO:iea[2009-02-17]
OMIM:180900	Rutherfurd syndrome		HP:0006352	OMIM:180900	IEA					P	HPO:iea[2009-02-17]
OMIM:180900	Rutherfurd syndrome		HP:0000006	OMIM:180900	IEA					I	HPO:iea[2009-02-17]
OMIM:173650	Kindler syndrome		HP:0002025	PMID:12668616	PCS		1/11			P	HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0001030	OMIM:173650	IEA					P	HPO:iea[2009-02-17]
OMIM:173650	Kindler syndrome		HP:0031045	PMID:12668616	PCS	HP:0003577	11/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0005590	OMIM:173650	IEA					P	HPO:iea[2009-02-17]
OMIM:173650	Kindler syndrome		HP:6000714	PMID:14962093	PCS		3/3			P	HPO:probinson[2024-05-09]
OMIM:173650	Kindler syndrome		HP:0001807	OMIM:173650	TAS					P	HPO:probinson[2009-02-17]
OMIM:173650	Kindler syndrome		HP:0010450	PMID:12668616	PCS		1/11			P	HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0007488	OMIM:173650	IEA					P	HPO:iea[2009-02-17]
OMIM:173650	Kindler syndrome		HP:0000972	PMID:12668616	PCS		4/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0001741	PMID:12668616	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0001029	PMID:12668616	PCS		11/11		HP:0003676	P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0200020	PMID:21683471	PCS					P	HPO:probinson[2017-05-28]
OMIM:173650	Kindler syndrome		HP:0000670	PMID:12668616	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0000230	PMID:12668616	PCS		8/11			P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0002015	PMID:12668616	PCS		6/11			P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0000992	PMID:12668616	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0004334	PMID:12668616	PCS		11/11			P	HPO:probinson[2009-02-17];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0005585	OMIM:173650	TAS					P	HPO:iea[2009-02-17]
OMIM:173650	Kindler syndrome		HP:0100585	PMID:12668616	PCS		9/11			P	HPO:probinson[2021-02-26];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0000704	OMIM:173650	IEA					P	HPO:iea[2009-02-17]
OMIM:173650	Kindler syndrome		HP:0008661	PMID:12668616	PCS		4/22			P	HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0009775	OMIM:173650	TAS					P	HPO:probinson[2009-02-17]
OMIM:173650	Kindler syndrome		HP:0430007	PMID:21683471	PCS					P	HPO:probinson[2017-05-28]
OMIM:173650	Kindler syndrome		HP:0000007	PMID:12668616	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-26]
OMIM:173650	Kindler syndrome		HP:0002745	PMID:12668616	PCS		8/11			P	HPO:probinson[2021-02-26]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0003621	PMID:31755148	PCS		5/18			C	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0001300	PMID:31755148	PCS		1/51			P	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0003596	PMID:31755148	PCS		6/18			C	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0001332	PMID:31755148	PCS		3/51			P	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0001266	OMIM:125370	TAS					P	HPO:iea[2009-02-17]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0001250	PMID:31755148	PCS		24/51			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0003584	PMID:31755148	PCS		1/18			C	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0001251	PMID:31755148	PCS		28/51			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0002072	PMID:31755148	PCS		24/51			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0002172	PMID:31755148	PCS		24/51			P	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0000726	PMID:31755148	PCS		18/51			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0011462	PMID:31755148	PCS		6/18			C	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0007047	PMID:20500452	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0000006	PMID:8136840	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0001249	PMID:31755148	PCS		8/51			P	HPO:probinson[2022-08-16]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0003743	OMIM:125370	TAS					I	HPO:iea[2009-02-17]
OMIM:125370	Dentatorubral-pallidoluysian atrophy		HP:0001336	PMID:31755148	PCS		2/51			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0005469	PMID:24501276	PCS		3/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0002069	PMID:24501276	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0000343	PMID:24501276	PCS		1/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0000233	PMID:24501276	PCS		3/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0000463	PMID:24501276	PCS		3/3			P	HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0000193	PMID:24501276	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0001263	PMID:24501276	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0001252	PMID:24501276	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0003593	OMIM:615942	TAS					C	HPO:skoehler[2015-12-30]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0005280	PMID:24501276	PCS		3/3			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0000007	PMID:24501276	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0001763	PMID:24626631	PCS		4/4			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0007359	PMID:24501276	PCS		1/3			P	HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0001249	PMID:24501276	PCS		3/3			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-06-15]
OMIM:615942	Intellectual developmental disorder, autosomal recessive 44		HP:0000049	PMID:24501276	PCS		1/2			P	HPO:probinson[2022-06-15]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0001265	OMIM:605589	IEA					P	HPO:iea[2009-02-17]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0003431	OMIM:605589	IEA				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0003693	OMIM:605589	TAS					P	HPO:probinson[2012-07-16]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0003581	OMIM:605589	TAS					C	HPO:probinson[2009-02-17]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0001284	OMIM:605589	IEA					P	HPO:iea[2009-02-17]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0002460	OMIM:605589	TAS					P	HPO:probinson[2012-07-16]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0000007	OMIM:605589	IEA					I	HPO:iea[2009-02-17]
OMIM:605589	Charcot-Marie-Tooth disease, axonal, type 2B2		HP:0002936	OMIM:605589	IEA					P	HPO:iea[2009-02-17]
OMIM:177350	Pseudoatrophoderma colli		HP:0000006	OMIM:177350	IEA					I	HPO:iea[2009-02-17]
OMIM:177350	Pseudoatrophoderma colli		HP:0000951	OMIM:177350	IEA					P	HPO:iea[2009-02-17]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001561	PMID:24319099	PCS		0/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0003577	PMID:26257172	PCS		1/1			C	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001761	PMID:26257172	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001371	OMIM:616287	TAS				HP:0012839	P	HPO:skoehler[2015-07-26]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0003693	PMID:26257172	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0011968	PMID:26257172	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0005684	PMID:24319099	PCS		2/2			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001252	PMID:24319099	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001284	PMID:26257172;PMID:24319099	PCS		3/3			P	HPO:probinson[2023-05-08];HPO:skoehler[2015-07-26]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0007182	PMID:26257172	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0034197	PMID:24319099	PCS		2/2			C	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0200136	OMIM:616287	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0000007	PMID:24319099	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001349	PMID:24319099	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001558	PMID:24319099	PCS		2/2			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0002936	PMID:26257172	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001605	PMID:26257172	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001522	PMID:24319099	PCS		1/2			C	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0003811	PMID:24319099	PCS		1/2			C	HPO:probinson[2023-05-08]
OMIM:616287	Lethal congenital contracture syndrome 8		HP:0001765	PMID:26257172	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:137760	Glaucoma, primary open angle		HP:0012108	OMIM:137760	TAS					P	HPO:skoehler[2009-02-17]
OMIM:137760	Glaucoma, primary open angle		HP:0000006	OMIM:137760	IEA					I	HPO:iea[2009-02-17]
OMIM:137760	Glaucoma, primary open angle		HP:0000545	OMIM:137760	IEA					P	HPO:iea[2009-02-17]
OMIM:237900	Hyperbilirubinemia, familial transient neonatal		HP:0001343	OMIM:237900	IEA					P	HPO:iea[2009-02-17]
OMIM:237900	Hyperbilirubinemia, familial transient neonatal		HP:0008176	PMID:11061796	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-11]
OMIM:237900	Hyperbilirubinemia, familial transient neonatal		HP:0000007	PMID:11061796	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-11]
OMIM:237900	Hyperbilirubinemia, familial transient neonatal		HP:0000952	PMID:11061796	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-11]
OMIM:237900	Hyperbilirubinemia, familial transient neonatal		HP:0003623	PMID:11061796	PCS					C	HPO:probinson[2022-06-11]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0002982	PMID:20602915	PCS		5/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0002983	OMIM:600383	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0001773	PMID:20602915	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000365	PMID:20602915	PCS		1/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0005694	OMIM:600383	IEA					P	HPO:iea[2009-02-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0005891	OMIM:600383	IEA					P	HPO:iea[2009-02-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0001196	OMIM:600383;PMID:20602915	PCS		6/9			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0001193	OMIM:600383	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0005096	PMID:20602915	PCS		4/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0010743	PMID:20602915	PCS		4/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0010292	PMID:20602915	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0100329	PMID:20602915	PCS		5/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0009487	PMID:20602915	PCS		5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0100328	PMID:20602915	PCS		5/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000316	OMIM:600383	IEA					P	HPO:iea[2009-02-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0001786	PMID:20602915	PCS		5/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0009701	OMIM:600383	TAS					P	HPO:skoehler[2015-12-30]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0003468	OMIM:600383	IEA					P	HPO:iea[2009-02-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0009803	PMID:20602915	PCS		5/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000494	PMID:20602915	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0003027	PMID:20602915	PCS		5/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0001561	PMID:20602915	PCS		2/4			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0001263	PMID:20602915	PCS		0/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000308	OMIM:600383	IEA					P	HPO:iea[2009-02-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000506	PMID:20602915	PCS		5/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000508	PMID:20602915	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000444	OMIM:600383	IEA					P	HPO:iea[2009-02-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000006	PMID:20602915	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000347	PMID:20602915	PCS		5/5		HP:0012825	P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000545	PMID:20602915	PCS		2/5			P	HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0000126	PMID:20602915	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0008845	OMIM:600383	IEA					P	HPO:iea[2009-02-17]
OMIM:600383	Mesomelia-Synostoses syndrome		HP:0001611	PMID:20602915	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-08]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0002354	OMIM:608907	TAS				HP:0003676	P	HPO:skoehler[2017-07-13]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0000716	OMIM:608907	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0002120	OMIM:608907	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0003584	PMID:26141617	PCS					C	HPO:probinson[2022-03-26]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0002185	OMIM:608907	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0000734	OMIM:608907	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0410170	OMIM:608907	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0002071	OMIM:608907	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0100256	OMIM:608907	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0000006	OMIM:608907	TAS					I	HPO:skoehler[2017-07-13]
OMIM:608907	Alzheimer disease 9, susceptibility to		HP:0002511	PMID:26141617	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:617827	Immunodeficiency 55		HP:0002014	PMID:28414293	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0000252	PMID:28414293	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0004322	PMID:28414293	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0001581	OMIM:617827	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617827	Immunodeficiency 55		HP:0034197	PMID:28414293	PCS		5/5			C	HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0008064	PMID:28414293	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0000958	PMID:28414293	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0002719	PMID:28414293	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0001999	PMID:28414293	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0000007	PMID:28414293	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0000964	PMID:28414293	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0002716	PMID:28414293	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0001888	PMID:28414293	PCS		5/5			P	HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0008897	PMID:28414293	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0001511	PMID:28414293	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0002863	PMID:28414293	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0040219	PMID:28414293	PCS		5/5			P	HPO:probinson[2022-09-25]
OMIM:617827	Immunodeficiency 55		HP:0001875	PMID:28414293	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003236	PMID:32493488;OMIM:164310	PCS		3/11			P	HPO:probinson[2021-10-16];HPO:probinson[2012-04-11]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0010628	OMIM:164310	TAS					P	HPO:probinson[2012-04-11]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003596	PMID:31332380	PCS		1/3			C	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003693	PMID:32493488	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003394	PMID:32493488	PCS		1/1			P	HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001251	PMID:31332380	PCS		1/4			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002460	PMID:21242490;PMID:32493488;PMID:31332380	PCS		39/52			P	HPO:probinson[2021-07-02];HPO:probinson[2012-04-11];HPO:probinson[2021-07-02];HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0012444	PMID:31332380	PCS		3/3			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0032341	PMID:21242490	PCS		7/47			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0011462	PMID:31332380	PCS		1/3			C	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0009027	OMIM:164310	TAS					P	HPO:probinson[2012-04-11]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003805	PMID:21242490;PMID:32493488	PCS		13/13			P	HPO:probinson[2012-04-11];HPO:probinson[2021-07-02];HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002835	OMIM:164310	IEA					P	HPO:skoehler[2018-10-08]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0000218	OMIM:164310	TAS					P	HPO:probinson[2012-04-11]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001824	OMIM:164310	IEA					P	HPO:skoehler[2019-09-07]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0008756	OMIM:164310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001324	PMID:32493488	PCS		1/1			P	HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003701	PMID:21242490;PMID:31332380	PCS		20/51			P	HPO:probinson[2021-07-02];HPO:probinson[2012-04-11];HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001488	PMID:32493488	PCS		1/1			P	HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0000597	PMID:21242490	PCS		39/47			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0004757	PMID:31332380	PCS		1/3			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001644	PMID:31332380	PCS		1/3			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002058	PMID:32493488	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-05-14]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002015	PMID:21242490;PMID:32493488;PMID:31332380	PCS		40/54			P	HPO:probinson[2021-07-02];HPO:probinson[2012-04-11];HPO:probinson[2021-07-02];HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003621	PMID:31332380	PCS		1/3			C	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001288	OMIM:164310	TAS					P	HPO:probinson[2012-04-11]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002098	PMID:32493488	PCS		1/1			P	HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001260	PMID:31332380	PCS		6/6			P	HPO:probinson[2012-04-11];HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001284	OMIM:164310	TAS					P	HPO:probinson[2012-04-11]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0100284	PMID:21242490	PCS		8/16			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0012416	PMID:21242490	PCS		8/47			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002091	OMIM:164310	TAS					P	HPO:skoehler[2017-07-13]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001618	PMID:32493488	PCS		1/1			P	HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001639	PMID:32493488	PCS		1/1			P	HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0000407	PMID:21242490	PCS		2/47			P	HPO:probinson[2012-04-11];HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0000508	PMID:21242490;PMID:31332380	TAS		52/53			P	HPO:probinson[2012-04-11];HPO:probinson[2021-07-02];HPO:probinson[2021-07-02];HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003736	OMIM:164310	IEA					P	HPO:skoehler[2018-10-08]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002747	PMID:31332380	PCS	HP:0003596	2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0002500	PMID:31332380	PCS		2/3			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0000006	PMID:31332380	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003677	OMIM:164310	TAS					C	HPO:skoehler[2012-10-17]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001337	PMID:31332380	PCS		1/4			P	HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003458	PMID:21242490;PMID:31332380	PCS		18/19			P	HPO:probinson[2021-07-02];HPO:probinson[2012-04-11];HPO:probinson[2021-07-02]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0000544	PMID:32493488;PMID:31332380	PCS		4/5			P	HPO:probinson[2012-04-11];HPO:probinson[2021-07-02];HPO:probinson[2021-10-16]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0003557	OMIM:164310	TAS					P	HPO:probinson[2012-04-11]
OMIM:164310	Oculopharyngodistal myopathy 1		HP:0001611	PMID:31332380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-02]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0003038	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0002089	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000123	OMIM:208500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0004322	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0001156	OMIM:208500	TAS					P	HPO:skoehler[2014-11-26]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000083	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0001395	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0010444	OMIM:208500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0012622	OMIM:208500	TAS					P	HPO:probinson[2014-01-19]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0001408	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0001829	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0010230	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0003828	OMIM:208500	TAS					M	HPO:skoehler[2013-04-18]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0008797	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000774	OMIM:208500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0001522	OMIM:208500	TAS		HP:0040283			C	HPO:probinson[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000773	OMIM:208500	TAS					P	HPO:probinson[2013-04-12]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000952	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0006557	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0009803	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0008839	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0003025	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0003022	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0001161	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000093	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0002093	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0100732	OMIM:208500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0002908	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0010582	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000107	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000888	OMIM:208500	TAS					P	HPO:probinson[2013-04-12]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000007	OMIM:208500	IEA					I	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0000546	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0001737	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0002205	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0002866	OMIM:208500	IEA					P	HPO:iea[2009-02-17]
OMIM:208500	Short-Rib thoracic dysplasia 1 with or without polydactyly		HP:0006644	OMIM:208500	IEA					P	HPO:skoehler[2015-01-27]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001298	PMID:20693550	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0008947	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002421	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0000365	PMID:19526370	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002045	PMID:17668387	PCS	HP:0003623	3/3			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001252	PMID:17668387	PCS	HP:0003623	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0012707	PMID:20693550	PCS					P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003593	PMID:19526370	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0032653	PMID:20693550;PMID:19526370	PCS		3/3			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001270	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0031964	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0007183	PMID:20693550	PCS		1/2			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0009141	PMID:17668387	PCS					P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001508	PMID:20693550	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0500181	PMID:17668387	PCS					P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0000975	PMID:19526370	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001943	PMID:17668387	PCS	HP:0003623				P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001943	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001943	PMID:20693550	PCS		2/2			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003648	PMID:17668387	PCS	HP:0003623	3/3			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002878	PMID:20693550	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001522	PMID:20693550	PCS		1/2			C	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003128	PMID:17668387	PCS	HP:0003623	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003128	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003128	PMID:20693550	PCS		2/2			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003623	PMID:17668387	PCS		3/3			C	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0008936	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003202	PMID:20693550	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0031956	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0008935	PMID:20693550	PCS		2/2			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002059	OMIM:245400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0011924	PMID:17668387	PCS					P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0011968	PMID:19526370	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002154	PMID:17668387	PCS					P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001263	PMID:20693550	PCS				HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001284	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002490	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0011923	PMID:17668387	PCS					P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002093	PMID:17668387	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0032988	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003819	PMID:19526370	PCS		1/1			C	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0012120	PMID:17668387	PCS	HP:0003623	3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0012120	PMID:19526370	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0012120	PMID:20693550	PCS		2/2			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0000007	PMID:17668387	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0008347	PMID:17668387	PCS					P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001511	PMID:17668387	PCS	HP:0011461	2/3			P	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0003811	PMID:17668387	PCS		3/3			C	HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0001510	PMID:20693550	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-11]
OMIM:245400	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)		HP:0002643	PMID:17668387	PCS					P	HPO:probinson[2020-10-11]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000164	OMIM:618282	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0003212	PMID:29907690	PCS		6/7			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0001596	OMIM:618282	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0031292	PMID:29907690	PCS		2/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0002719	OMIM:618282	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000958	PMID:29907690	PCS		1/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0006532	PMID:29907690	PCS		2/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000218	OMIM:618282	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0001642	PMID:29907690	PCS		1/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0025616	PMID:29907690	PCS		4/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0002754	PMID:29907690	PCS		1/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0001880	PMID:29907690	PCS		1/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0001047	PMID:29907690	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0001382	OMIM:618282	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0002110	OMIM:618282	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0001581	OMIM:618282	IEA		11/11			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0011108	PMID:29907690	PCS		2/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0032326	PMID:29907690	PCS		4/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0009098	PMID:29907690	PCS		3/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0002728	PMID:29907690	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000403	OMIM:618282	IEA		4/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000964	PMID:29907690	PCS		8/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000007	PMID:29907690	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000989	OMIM:618282	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0002205	OMIM:618282	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0003416	PMID:29907690	PCS		1/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0001631	PMID:29907690	PCS		1/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000347	OMIM:618282	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0002720	PMID:29907690	PCS		1/11			P	HPO:probinson[2022-12-21]
OMIM:618282	Hyper-IgE recurrent infection syndrome 3, autosomal recessive		HP:0000445	OMIM:618282	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300148	Mehmo syndrome		HP:0002465	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000486	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000343	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0002540	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001250	PMID:28055140	PCS		7/12	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0002066	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001290	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0410030	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0003828	OMIM:300148	IEA					M	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000718	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000437	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001943	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0002119	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000455	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001249	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001347	PMID:28055140	PCS		2/6	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0008936	PMID:28055140	PCS		3/7	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0000252	PMID:28055140	PCS		9/9	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0000054	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000175	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000750	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000276	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001288	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0003487	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0002079	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0003561	PMID:28055140	PCS		5/7	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0000194	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001263	PMID:28055140	PCS		10/10	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0001285	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0400000	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0001518	PMID:28055140	PCS		6/9	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0001419	PMID:28055140	PCS					I	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0000824	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000823	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0002307	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000026	PMID:28055140	PCS		9/11	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0000400	OMIM:300148	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300148	Mehmo syndrome		HP:0001257	PMID:28055140	PCS		3/8	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0001513	PMID:28055140	PCS	HP:0003593	8/10	MALE		P	HP:probinson[2018-04-15]
OMIM:300148	Mehmo syndrome		HP:0000545	OMIM:300148	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300148	Mehmo syndrome		HP:0000687	OMIM:300148	IEA					P	HPO:skoehler[2019-04-18]
OMIM:608091	Joubert syndrome 2		HP:0002365	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001250	PMID:20036350	PCS		1/13			P	HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000083	PMID:20036350	PCS		2/13			P	HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0001252	PMID:20036350	PCS		13/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0001251	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001273	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0002084	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0011933	OMIM:608091	TAS					P	HPO:probinson[2012-06-10]
OMIM:608091	Joubert syndrome 2		HP:0000639	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001508	PMID:20036350	PCS					P	HPO:skoehler[2013-06-23];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000617	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000657	PMID:20036350	PCS					P	HPO:probinson[2012-04-01];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000316	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0002419	PMID:20036350	PCS		13/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000238	PMID:20036350	PCS		1/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000218	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0002876	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000256	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000556	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001249	PMID:20036350	PCS		13/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0002335	PMID:20036350	PCS					P	HPO:probinson[2012-06-10];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0001760	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001583	PMID:20036350	PCS		11/13			P	HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0002871	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001162	PMID:20036350	PCS	HP:0003577	2/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000050	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001263	PMID:20036350	PCS		13/13			P	HPO:probinson[2012-04-01];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0002195	PMID:20036350	PCS					P	HPO:probinson[2012-06-10];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000570	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0002790	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000090	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0005280	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0100951	OMIM:608091	PCS					P	HPO:probinson[2012-04-01]
OMIM:608091	Joubert syndrome 2		HP:0011330	PMID:20036350	PCS		1/13			P	HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0002508	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000107	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0007772	OMIM:608091	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608091	Joubert syndrome 2		HP:0000568	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000007	PMID:20036350	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000505	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0001830	PMID:20036350	PCS	HP:0003577	3/13			P	HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0002007	PMID:20036350	PCS		6/13			P	HPO:skoehler[2013-06-23];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000565	PMID:20036350	PCS		5/13			P	HPO:skoehler[2013-06-23];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0000268	PMID:20036350	PCS		6/13			P	HPO:skoehler[2013-06-23];HPO:probinson[2022-06-23]
OMIM:608091	Joubert syndrome 2		HP:0002404	OMIM:608091	TAS					P	HPO:probinson[2012-06-10]
OMIM:608091	Joubert syndrome 2		HP:0000369	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000567	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:608091	Joubert syndrome 2		HP:0000588	OMIM:608091	IEA					P	HPO:iea[2009-02-17]
OMIM:241100	Hypogonadism, malehypogonadism and testicular atrophy, included		HP:0000054	OMIM:241100	IEA					P	HPO:iea[2009-02-17]
OMIM:241100	Hypogonadism, malehypogonadism and testicular atrophy, included		HP:0000771	OMIM:241100	IEA					P	HPO:iea[2009-02-17]
OMIM:241100	Hypogonadism, malehypogonadism and testicular atrophy, included		HP:0000007	OMIM:241100	IEA					I	HPO:iea[2009-02-17]
OMIM:241100	Hypogonadism, malehypogonadism and testicular atrophy, included		HP:0000029	OMIM:241100	IEA					P	HPO:skoehler[2015-12-30]
OMIM:241100	Hypogonadism, malehypogonadism and testicular atrophy, included		HP:0000026	OMIM:241100	IEA					P	HPO:iea[2009-02-17]
OMIM:241100	Hypogonadism, malehypogonadism and testicular atrophy, included		HP:0000047	OMIM:241100	IEA					P	HPO:iea[2009-02-17]
OMIM:269840	Immunodeficiency 48		HP:0005401	PMID:2511270	PCS		1/1			P	HPO:skoehler[2013-08-12];HPO:probinson[2024-03-09]
OMIM:269840	Immunodeficiency 48		HP:0005422	PMID:11412303	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:269840	Immunodeficiency 48		HP:0002240	OMIM:269840	IEA					P	HPO:iea[2009-02-17]
OMIM:269840	Immunodeficiency 48		HP:0003593	PMID:2511270;PMID:11412303	PCS		2/2			C	HPO:probinson[2024-03-09];HPO:probinson[2022-09-24]
OMIM:269840	Immunodeficiency 48		HP:0002090	OMIM:269840	TAS					P	HPO:skoehler[2009-02-17]
OMIM:269840	Immunodeficiency 48		HP:0010975	PMID:2511270	PCS		0/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-09]
OMIM:269840	Immunodeficiency 48		HP:0001508	OMIM:269840	IEA					P	HPO:iea[2009-02-17]
OMIM:269840	Immunodeficiency 48		HP:0000007	PMID:8124727	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:269840	Immunodeficiency 48		HP:0000964	OMIM:269840	TAS					P	HPO:skoehler[2013-08-12]
OMIM:269840	Immunodeficiency 48		HP:0020102	PMID:2511270	PCS	HP:0003593	1/1			P	HPO:probinson[2024-03-09]
OMIM:269840	Immunodeficiency 48		HP:0002205	PMID:11412303	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:269840	Immunodeficiency 48		HP:0001744	OMIM:269840	IEA					P	HPO:iea[2009-02-17]
OMIM:269840	Immunodeficiency 48		HP:0003347	PMID:11412303	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:269840	Immunodeficiency 48		HP:0003139	OMIM:269840	IEA					P	HPO:iea[2009-02-17]
OMIM:269840	Immunodeficiency 48		HP:0002028	PMID:2511270	PCS		1/1			P	HPO:probinson[2024-03-09]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001276	PMID:31723249	PCS		3/27			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000286	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000582	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000486	PMID:31723249	PCS		3/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001212	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000463	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001250	PMID:31723249	PCS		3/26			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001252	PMID:31723249	PCS		10/27			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000639	PMID:31723249	PCS		2/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000319	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0011220	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0012450	PMID:31723249	PCS		6/26			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000316	PMID:31723249	PCS		14/43			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000954	PMID:31723249	PCS		2/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000414	PMID:31723249	PCS		4/30			P	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0002119	PMID:31723249	PCS		1/12			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000219	PMID:31723249	PCS		3/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000218	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000378	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001249	PMID:31723249	PCS					P	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000252	PMID:31723249	PCS		4/28			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000750	PMID:31723249	PCS		26/27			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001321	PMID:31723249	PCS		1/12			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000331	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0011968	PMID:31723249	PCS		8/26			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0005487	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001263	PMID:31723249	PCS		27/28			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0032388	PMID:31723249	PCS		1/12			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0005280	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000729	PMID:31723249	PCS		17/27			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000307	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0004209	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001357	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000664	PMID:31723249	PCS		1/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0007018	PMID:31723249	PCS		9/27			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0001510	PMID:31723249	PCS		11/27			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000322	PMID:31723249	PCS		3/15			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000006	PMID:31723249	PCS					I	HPO:probinson[2021-04-27];HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000347	PMID:31723249	PCS		13/28			P	HPO:probinson[2021-04-27]
OMIM:619188	Intellectual developmental disorder, autosomal dominant 64		HP:0000369	PMID:31723249	PCS		2/15			P	HPO:probinson[2021-04-27]
OMIM:619836	Hypoalphalipoproteinemia, primary, 2, intermediate		HP:0003233	PMID:2512329	PCS					P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:619836	Hypoalphalipoproteinemia, primary, 2, intermediate		HP:0031799	PMID:2512329	PCS					P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:619836	Hypoalphalipoproteinemia, primary, 2, intermediate		HP:0000006	PMID:2512329	PCS					I	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:176700	Prognathism, mandibular		HP:0001363	OMIM:176700	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:176700	Prognathism, mandibular		HP:0003829	OMIM:176700	TAS					I	HPO:skoehler[2017-07-13]
OMIM:176700	Prognathism, mandibular		HP:0007651	OMIM:176700	IEA					P	HPO:iea[2009-02-17]
OMIM:176700	Prognathism, mandibular		HP:0000179	OMIM:176700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176700	Prognathism, mandibular		HP:0000303	OMIM:176700	IEA					P	HPO:iea[2009-02-17]
OMIM:176700	Prognathism, mandibular		HP:0000006	OMIM:176700	TAS					I	HPO:skoehler[2017-07-13]
OMIM:103200	Adiposis dolorosa		HP:0003596	OMIM:103200	IEA					C	HPO:iea[2009-02-17]
OMIM:103200	Adiposis dolorosa		HP:0003270	OMIM:103200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:103200	Adiposis dolorosa		HP:0012532	OMIM:103200	TAS					P	HPO:skoehler[2015-01-04]
OMIM:103200	Adiposis dolorosa		HP:0012378	OMIM:103200	TAS					P	HPO:skoehler[2015-01-04]
OMIM:103200	Adiposis dolorosa		HP:0002829	OMIM:103200	TAS					P	HPO:skoehler[2015-01-04]
OMIM:103200	Adiposis dolorosa		HP:0000716	OMIM:103200	TAS					P	HPO:skoehler[2015-12-30]
OMIM:103200	Adiposis dolorosa		HP:0003828	OMIM:103200	TAS					M	HPO:skoehler[2015-12-30]
OMIM:103200	Adiposis dolorosa		HP:0000739	OMIM:103200	TAS					P	HPO:skoehler[2015-01-04]
OMIM:103200	Adiposis dolorosa		HP:0007596	OMIM:103200	IEA					P	HPO:iea[2009-02-17]
OMIM:103200	Adiposis dolorosa		HP:0002019	OMIM:103200	TAS					P	HPO:skoehler[2015-01-04]
OMIM:103200	Adiposis dolorosa		HP:0000006	OMIM:103200	IEA					I	HPO:iea[2009-02-17]
OMIM:103200	Adiposis dolorosa		HP:0001513	OMIM:103200	IEA					P	HPO:iea[2009-02-17]
DECIPHER:37	3q29 microdeletion syndrome		HP:0000276	DECIPHER:37	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:37	3q29 microdeletion syndrome		HP:0000426	DECIPHER:37	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:37	3q29 microdeletion syndrome		HP:0000322	DECIPHER:37	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:37	3q29 microdeletion syndrome		HP:0001249	DECIPHER:37	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614255	NESCAV syndrome		HP:0003477	PMID:25265257	PCS		7/14			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0003676	OMIM:614255	TAS					C	HPO:skoehler[2015-12-30]
OMIM:614255	NESCAV syndrome		HP:0002540	OMIM:614255	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614255	NESCAV syndrome		HP:0001272	PMID:25265257	PCS		9/14			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0001371	OMIM:614255	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614255	NESCAV syndrome		HP:0001250	PMID:25265257	PCS		3/13			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0001251	PMID:25265257	PCS		3/12			P	HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0001290	OMIM:614255	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614255	NESCAV syndrome		HP:0000639	OMIM:614255	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614255	NESCAV syndrome		HP:0100704	OMIM:614255	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614255	NESCAV syndrome		HP:0001249	PMID:21376300;PMID:25265257	PCS		15/15			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0006855	PMID:21376300	PCS		1/1		HP:0012825	P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0001347	OMIM:614255	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614255	NESCAV syndrome		HP:0008936	PMID:21376300	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0002059	PMID:25265257	PCS		6/14			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0000252	PMID:25265257	PCS		4/14			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0001344	PMID:25265257	PCS		4/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0000750	PMID:25265257	PCS		11/14			P	HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0001762	OMIM:614255	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614255	NESCAV syndrome		HP:0003487	OMIM:614255	TAS					P	HPO:skoehler[2015-10-05]
OMIM:614255	NESCAV syndrome		HP:0001263	PMID:25265257	PCS		14/14			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0034353	PMID:21376300	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0000648	PMID:25265257	PCS		9/14			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0001257	PMID:25265257	PCS		13/14			P	HPO:probinson[2013-08-10];HPO:probinson[2023-02-07]
OMIM:614255	NESCAV syndrome		HP:0000006	PMID:21376300	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-02-07]
OMIM:606889	Alzheimer disease 4		HP:0006979	OMIM:606889	TAS					P	HPO:probinson[2012-07-16]
OMIM:606889	Alzheimer disease 4		HP:0003596	PMID:9007102;PMID:12925374	PCS		11/11			C	HPO:probinson[2012-07-16];HP:probinson[2019-06-11];ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0001289	PMID:12925374	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease 4		HP:0002354	PMID:9007102	PCS	HP:0003596	2/5			P	HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease-4		HP:0002354	PMID:30104866	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0002354	PMID:12925374	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0002197	PMID:30104866;PMID:12925374	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease 4		HP:0002186	PMID:9007102	PCS	HP:0003596	2/5			P	HP:probinson[2019-06-11];HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease-4		HP:0030784	PMID:12925374	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease 4		HP:0002185	PMID:9450781	PCS					P	HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease-4		HP:0031058	PMID:30104866;PMID:12925374	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease 4		HP:0100256	PMID:9450781	PCS					P	HPO:skoehler[2018-10-08];HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease 4		HP:0012662	PMID:19073399	PCS					P	HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease 4		HP:0100543	PMID:19073399	PCS					P	HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease 4		HP:0011970	PMID:9450781	PCS	HP:0003584	4/4			P	HPO:probinson[2012-07-18];HPO:probinson[2024-05-18]
OMIM:606889	Alzheimer disease 4		HP:0000726	PMID:9007102	PCS	HP:0003596	3/5			P	HPO:probinson[2012-07-16];HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease-4		HP:0000726	PMID:30104866	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0000726	PMID:12925374	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0000718	PMID:30104866;PMID:12925374	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0007112	PMID:30104866	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0000741	PMID:30104866	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:606889	Alzheimer disease 4		HP:0000006	PMID:9007102	PCS					I	HPO:probinson[2012-07-16];HP:probinson[2019-06-11]
OMIM:606889	Alzheimer disease 4		HP:0002511	PMID:30104866;PMID:12925374	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-18];HPO:skoehler[2015-01-19];HPO:probinson[2024-05-18]
OMIM:606889	Alzheimer disease-4		HP:0001336	PMID:12925374	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0000252	PMID:27737959	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0004322	PMID:27737959	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0001250	PMID:27737959	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0011343	PMID:27737959	PCS		1/2			P	HPO:probinson[2023-01-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0001518	PMID:27737959	PCS		1/2			P	HPO:probinson[2023-01-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0002509	PMID:27737959	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0003593	PMID:27737959	PCS		2/2			C	HPO:probinson[2023-01-18]
OMIM:617984	Microcephaly 22, primary, autosomal recessive		HP:0000007	PMID:27737959	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-01-18]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0003577	PMID:8755487	PCS		2/2			C	HPO:probinson[2023-01-17]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0003388	OMIM:616324	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0011968	OMIM:616324	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0001252	OMIM:616324	TAS	HP:0003623				P	HPO:skoehler[2015-05-31]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0003593	PMID:10962020	PCS		4/4			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-17]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0002093	OMIM:616324	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0030319	PMID:10962020	PCS		4/4			P	HPO:probinson[2023-01-17]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0030208	PMID:10962020	PCS		0/4			P	HPO:probinson[2023-01-17]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0000508	OMIM:616324	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0000602	PMID:10962020	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-01-17]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0030197	PMID:8755487	PCS		2/2			P	HPO:probinson[2023-01-17]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0000007	PMID:8755487	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-17]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0001319	OMIM:616324	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0001324	OMIM:616324	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0000467	OMIM:616324	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616324	Myasthenic syndrome, congenital, 4B, fast-channel		HP:0003403	PMID:10962020	PCS		4/4			P	HPO:probinson[2023-01-17]
OMIM:107700	Appendicitis, proneness to		HP:0002250	OMIM:107700	IEA					P	HPO:skoehler[2009-02-17]
OMIM:183400	Split lower lip		HP:0000164	OMIM:183400	IEA					P	HPO:iea[2009-02-17]
OMIM:183400	Split lower lip		HP:0000178	OMIM:183400	TAS					P	HPO:lccarmody[2018-10-03]
OMIM:183400	Split lower lip		HP:0002010	OMIM:183400	IEA					P	HPO:iea[2009-02-17]
OMIM:183400	Split lower lip		HP:0000196	OMIM:183400	TAS					P	HPO:lccarmody[2018-10-03]
OMIM:183400	Split lower lip		HP:0000006	OMIM:183400	IEA					I	HPO:iea[2009-02-17]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0030731	OMIM:610755	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0002893	OMIM:610755	IEA					P	HPO:iea[2009-02-17]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0008200	PMID:24819502	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0100570	OMIM:610755	TAS					P	HPO:skoehler[2015-04-05]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0006772	OMIM:610755	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0000821	PMID:24819502	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0000843	PMID:24819502	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0000845	OMIM:610755	IEA					P	HPO:iea[2009-02-17]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0000872	PMID:24819502	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0030405	PMID:24819502	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0000006	OMIM:610755	IEA					I	HPO:iea[2009-02-17]
OMIM:610755	Multiple endocrine neoplasia, type IV		HP:0002897	PMID:24819502	TAS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2021-05-08]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0000252	OMIM:600546	PCS					P	HPO:probinson[2012-03-16]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0003220	OMIM:600546	PCS					P	HPO:probinson[2012-03-16]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0001263	OMIM:600546	IEA					P	HPO:iea[2009-02-17]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0001999	OMIM:600546	PCS					P	HPO:probinson[2012-03-16]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0000007	OMIM:600546	IEA					I	HPO:iea[2009-02-17]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0008897	OMIM:600546	PCS					P	HPO:probinson[2012-03-16]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0001511	OMIM:600546	PCS					P	HPO:probinson[2012-03-16]
OMIM:600546	Intrauterine growth retardation with increased mitomycin C sensitivity		HP:0001876	OMIM:600546	PCS					P	HPO:probinson[2012-03-16]
OMIM:618309	Epidermodysplasia verruciformis, susceptibility to, 5		HP:0005403	PMID:25981006	PCS		3/3			P	HPO:probinson[2020-08-02]
OMIM:618309	Epidermodysplasia verruciformis, susceptibility to, 5		HP:0032160	PMID:25981006	PCS		2/3			P	HPO:probinson[2020-08-02]
OMIM:618309	Epidermodysplasia verruciformis, susceptibility to, 5		HP:0006739	PMID:25981006	PCS		1/3			P	HPO:probinson[2020-08-02]
OMIM:618309	Epidermodysplasia verruciformis, susceptibility to, 5		HP:0000007	PMID:25981006	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-08-02]
OMIM:618309	Epidermodysplasia verruciformis, susceptibility to, 5		HP:0001888	PMID:25981006	PCS		3/3			P	HPO:probinson[2020-08-02]
OMIM:618309	Epidermodysplasia verruciformis, susceptibility to, 5		HP:0020114	PMID:25981006	PCS					P	HPO:probinson[2020-08-02]
OMIM:618309	Epidermodysplasia verruciformis, susceptibility to, 5		HP:0200043	PMID:25981006	PCS					P	HPO:probinson[2020-08-02]
OMIM:155720	Melanoma, uveal		HP:0007716	OMIM:155720	TAS					P	HPO:probinson[2009-02-17]
OMIM:155720	Melanoma, uveal		HP:0000006	OMIM:155720	TAS					I	HPO:probinson[2009-02-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000286	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0001773	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000122	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0004322	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000089	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0001250	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0002384	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0011856	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0045075	OMIM:614527	TAS					P	HPO:probinson[2022-05-08]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0004719	OMIM:614527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000717	OMIM:614527	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000998	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0031909	OMIM:614527	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0100807	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000278	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0001249	OMIM:614527	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0009824	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0002553	OMIM:614527	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000010	OMIM:614527	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000494	OMIM:614527	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000177	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0005343	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0010511	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0008404	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000003	OMIM:614527	TAS	HP:0003577				P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000006	OMIM:614527	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000126	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000324	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0003774	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0001792	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0001795	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000540	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0002164	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0003250	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000218	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000411	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0002910	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000138	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0004279	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0002650	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000750	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0008619	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000272	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000151	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0005280	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0100753	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0008661	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000107	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000348	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0002007	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0005999	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000347	OMIM:614527	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000303	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000666	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:614527	Chromosome 17q12 deletion syndrome		HP:0000028	OMIM:614527	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:115310	Paragangliomas 4		HP:0006824	OMIM:115310	TAS					P	HPO:probinson[2016-07-19]
OMIM:115310	Paragangliomas 4		HP:0002331	OMIM:115310	IEA					P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0006737	PMID:11404820	PCS		5/9			P	HPO:iea[2018-03-07];HPO:probinson[2023-03-16]
OMIM:115310	Paragangliomas 4		HP:0006748	PMID:11404820	PCS		2/9			P	HPO:iea[2018-03-07];HPO:probinson[2023-03-16]
OMIM:115310	Paragangliomas 4		HP:0008629	OMIM:115310	TAS					P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0002640	OMIM:115310	IEA					P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0003001	OMIM:115310	IEA					P	HPO:iea[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0003581	PMID:11404820	PCS		9/9			C	HPO:iea[2018-03-07];HPO:probinson[2023-03-16]
OMIM:115310	Paragangliomas 4		HP:0005584	OMIM:115310	IEA					P	HPO:iea[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0011976	OMIM:115310	TAS					P	HPO:probinson[2016-07-22]
OMIM:115310	Paragangliomas 4		HP:0100723	OMIM:115310	TAS		HP:0040283			P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0003829	OMIM:115310	TAS					I	HPO:skoehler[2013-04-02]
OMIM:115310	Paragangliomas 4		HP:0000975	OMIM:115310	TAS					P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0001649	OMIM:115310	TAS					P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0030074	OMIM:115310	TAS					P	HPO:skoehler[2015-01-20]
OMIM:115310	Paragangliomas 4		HP:0001962	OMIM:115310	TAS					P	HPO:iea[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0000740	OMIM:115310	IEA					P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0002668	OMIM:115310	TAS					P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0000006	PMID:11404820	PCS					I	HPO:iea[2018-03-07];HPO:probinson[2023-03-16]
OMIM:115310	Paragangliomas 4		HP:0003006	OMIM:115310	IEA		HP:0040283			P	HPO:skoehler[2018-03-07]
OMIM:115310	Paragangliomas 4		HP:0002864	PMID:11404820	PCS		3/9			P	HPO:skoehler[2018-03-07];HPO:probinson[2023-03-16]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0002465	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0010529	PMID:25381298	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0001288	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0031936	PMID:25381298	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0003473	PMID:25381298	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0001260	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0001263	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0001251	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0001284	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0034197	PMID:25381298	PCS		1/1			C	HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0006380	PMID:25381298	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0000508	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0001558	PMID:25381298	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0000006	PMID:25381298	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-27]
OMIM:616330	Myasthenic syndrome, congenital, 18		HP:0002643	PMID:25381298	PCS		1/1			P	HPO:probinson[2022-09-27]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0032528	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0002089	PMID:28040730	PCS	HP:0003577	1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0001790	PMID:28040730	PCS	HP:0011461	1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0002092	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0032653	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0011923	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0000007	PMID:28040730	PCS					I	HPO:probinson[2020-12-01];HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0008358	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0003648	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0001638	PMID:28040730	PCS	HP:0011461	1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0001511	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0003811	PMID:28040730	PCS		1/1			C	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0005989	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0002643	PMID:28040730	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0001942	PMID:28040730	PCS	HP:0003623	1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0003128	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:619003	Mitochondrial complex I deficiency, nuclear type 35		HP:0003348	PMID:28040730	PCS		1/1			P	HPO:probinson[2020-12-01]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0003774	PMID:18268355	PCS		3/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0003621	PMID:18268355	PCS					C	HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0000100	PMID:18268355	PCS		6/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0000083	PMID:18268355	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0030949	PMID:18268355	PCS		5/5			P	HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0000093	PMID:18268355	PCS		8/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:6000428	PMID:18268355	PCS		5/5			P	HPO:probinson[2024-02-27]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0002907	PMID:18268355	PCS		3/6			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0011462	PMID:18268355	PCS					C	HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0000822	PMID:18268355	PCS		7/8			P	HPO:probinson[2009-02-17];HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0030162	PMID:18268355	PCS		5/5			P	HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0000006	PMID:18268355	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-07-17]
OMIM:601894	Glomerulopathy with fibronectin deposits 2		HP:0003677	PMID:18268355	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-17]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0002465	OMIM:618453	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0002059	OMIM:618453	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0000750	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0004322	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0001260	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0001263	OMIM:618453	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0011675	OMIM:618453	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0100660	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0012385	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0002808	OMIM:618453	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0001845	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0000007	PMID:30968111	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0004209	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:618453	Intellectual developmental disorder with short stature and variable skeletal anomalies		HP:0009778	PMID:30968111	PCS					P	HPO:probinson[2019-07-07]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0001166	OMIM:300799	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0009183	OMIM:300799	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0000708	OMIM:300799	IEA		HP:0040283			P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0000486	OMIM:300799	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0001519	OMIM:300799	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0001417	OMIM:300799	IEA					I	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0000768	OMIM:300799	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0000411	OMIM:300799	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0001763	OMIM:300799	IEA					P	HPO:skoehler[2013-01-11]
OMIM:300799	Intellectual developmental disorder, X-linked syndromic, Raymond type		HP:0001249	OMIM:300799	IEA		HP:0040280			P	HPO:skoehler[2013-01-09]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003202	PMID:27816943	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003555	PMID:27816943	PCS		1/4			P	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003687	PMID:27816943	PCS		4/4			P	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0002650	PMID:27816943	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003388	PMID:27816943	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0001382	PMID:27816943	PCS		3/5			P	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0002792	PMID:27816943	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003394	PMID:27816943	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0001252	PMID:27816943	PCS		3/5			P	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0002460	PMID:27816943	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0001270	PMID:27816943	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0100297	PMID:27816943	PCS		2/4			P	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0011463	PMID:27816943	PCS		5/5			C	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0008981	PMID:27816943	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0000007	PMID:27816943	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003805	PMID:27816943	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003307	PMID:27816943	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0002515	PMID:27816943	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0006466	PMID:27816943	PCS		1/5			P	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003803	PMID:27816943	PCS		4/4			P	HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003701	PMID:27816943	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003677	PMID:27816943	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-24]
OMIM:617760	Myopathy, centronuclear, 6, with fiber-type disproportion		HP:0003557	PMID:27816943	PCS		4/4			P	HPO:probinson[2023-02-24]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0003577	PMID:35087184	PCS		1/5			C	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000486	PMID:35087184	PCS		4/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0004322	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0001156	PMID:35087184	PCS		2/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0001252	PMID:35087184	PCS	HP:0011463	2/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0003593	PMID:35087184	PCS		4/5			C	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0010763	PMID:35087184	PCS		3/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0002080	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0031348	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0001629	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0011220	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000218	PMID:35087184	PCS		3/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0006895	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000455	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0002359	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0001348	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0001249	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0006956	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000750	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0003189	PMID:35087184	PCS		2/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000431	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0002650	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0005280	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0011448	PMID:35087184	PCS		5/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0008081	PMID:35087184	PCS		3/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000007	PMID:35087184	PCS					I	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000403	PMID:35087184	PCS		3/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000960	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000248	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:619995	Neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies		HP:0000445	PMID:35087184	PCS		1/5			P	HPO:probinson[2022-08-31]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0003621	PMID:16825436	PCS		5/15			C	HPO:probinson[2022-08-23]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0002155	PMID:16825436	PCS					P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0003593	PMID:16825436	PCS		6/15			C	HPO:probinson[2022-08-23]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0011900	PMID:16825436	PCS					P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0012177	PMID:16825436	PCS		13/13			P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0012156	PMID:16825436	PCS					P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0025708	PMID:16825436	PCS		1/15			C	HPO:probinson[2022-08-23]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0001903	PMID:16825436	PCS		12/14			P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0011463	PMID:16825436	PCS		1/15			C	HPO:probinson[2022-08-23]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0000007	PMID:16825436	PCS					I	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0001913	PMID:16825436	PCS		11/14			P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0001945	PMID:16825436	PCS					P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0001433	PMID:16825436	PCS					P	HPO:probinson[2013-03-30]
OMIM:608898	Hemophagocytic lymphohistiocytosis, familial, 3		HP:0003623	PMID:16825436	PCS		2/15			C	HPO:probinson[2022-08-23]
OMIM:278150	Hypotrichosis 8		HP:0000164	PMID:18297072	PCS		0/14			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:278150	Hypotrichosis 8		HP:0002224	PMID:18297072	PCS		14/14			P	HPO:skoehler[2009-02-17];HPO:probinson[2024-03-09]
OMIM:278150	Hypotrichosis 8		HP:0003577	PMID:18297072	PCS		14/14			C	HPO:probinson[2022-05-08]
OMIM:278150	Hypotrichosis 8		HP:0002286	OMIM:278150	IEA					P	HPO:iea[2009-02-17]
OMIM:278150	Hypotrichosis 8		HP:0045075	OMIM:278150	TAS					P	HPO:probinson[2022-05-08]
OMIM:278150	Hypotrichosis 8		HP:0011359	PMID:18297072	PCS		14/14			P	HPO:skoehler[2012-11-18];HPO:probinson[2024-03-09]
OMIM:278150	Hypotrichosis 8		HP:0001807	OMIM:278150	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:278150	Hypotrichosis 8		HP:0002209	PMID:18297072	PCS		14/14			P	HPO:skoehler[2012-11-18];HPO:probinson[2024-03-09]
OMIM:278150	Hypotrichosis 8		HP:0000007	PMID:18297072	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-05-08]
OMIM:278150	Hypotrichosis 8		HP:0000975	PMID:18297072	PCS		0/14			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-09]
OMIM:278150	Hypotrichosis 8		HP:0025249	OMIM:278150	IEA					P	HPO:skoehler[2018-10-08]
OMIM:278150	Hypotrichosis 8		HP:0001803	OMIM:278150	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:278150	Hypotrichosis 8		HP:0002208	PMID:18297072	PCS		14/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:278150	Hypotrichosis 8		HP:0000653	PMID:18297072	PCS		0/14			P	HPO:skoehler[2012-11-18];HPO:probinson[2024-03-09]
OMIM:278150	Hypotrichosis 8		HP:0002215	OMIM:278150	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613506	Agammaglobulinemia 5, autosomal dominant		HP:0000286	OMIM:613506	TAS					P	HPO:probinson[2013-08-10]
OMIM:613506	Agammaglobulinemia 5, autosomal dominant		HP:0004432	OMIM:613506	TAS					P	HPO:probinson[2013-08-10]
OMIM:613506	Agammaglobulinemia 5, autosomal dominant		HP:0000316	OMIM:613506	TAS				HP:0012825	P	HPO:probinson[2013-08-10]
OMIM:613506	Agammaglobulinemia 5, autosomal dominant		HP:0000218	OMIM:613506	TAS					P	HPO:probinson[2013-08-10]
OMIM:613506	Agammaglobulinemia 5, autosomal dominant		HP:0000006	OMIM:613506	TAS					I	HPO:probinson[2013-08-10]
OMIM:613506	Agammaglobulinemia 5, autosomal dominant		HP:0000369	OMIM:613506	TAS					P	HPO:probinson[2013-08-10]
OMIM:190440	Trigonocephaly 1		HP:0002245	OMIM:190440	IEA					P	HPO:iea[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0000286	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000582	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000384	OMIM:190440	IEA					P	HPO:iea[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0000252	OMIM:190440	IEA					P	HPO:iea[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0001363	OMIM:190440	IEA					P	HPO:iea[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0003577	PMID:11173846	PCS		1/1			C	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000431	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000343	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000750	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000243	PMID:11173846	PCS	HP:0003577	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000040	OMIM:190440	IEA					P	HPO:iea[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0003196	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0011330	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0000601	PMID:11173846	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0002705	PMID:11173846	PCS		1/1			P	HPO:probinson[2022-10-09]
OMIM:190440	Trigonocephaly 1		HP:0001539	OMIM:190440	IEA					P	HPO:iea[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0000664	OMIM:190440	TAS				HP:0012825	P	HPO:skoehler[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0008439	OMIM:190440	IEA					P	HPO:iea[2009-02-17]
OMIM:190440	Trigonocephaly 1		HP:0001249	PMID:11173846	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:190440	Trigonocephaly 1		HP:0000006	PMID:11173846	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-09]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0003676	OMIM:231550	IEA					C	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0001278	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0009916	OMIM:231550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0004322	OMIM:231550	TAS					P	HPO:probinson[2012-04-11]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0001251	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0012332	PMID:11062474	PCS		4/17			P	HPO:probinson[2012-04-11];HPO:probinson[2022-11-10]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0011463	PMID:11062474	PCS		4/14			C	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0011462	PMID:11062474	PCS		2/14			C	HPO:probinson[2022-11-10]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0007002	OMIM:231550	TAS					P	HPO:skoehler[2012-10-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000953	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0008259	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0004319	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0001324	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000972	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0001249	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0001347	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0003621	PMID:11062474	PCS		8/14			C	HPO:probinson[2022-11-10]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000252	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0003487	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0002571	PMID:11062474	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0001260	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0001263	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0008163	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000649	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000007	PMID:11062474	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000846	PMID:11062474	PCS		15/17			P	HPO:probinson[2022-11-10]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000648	OMIM:231550	IEA					P	HPO:iea[2009-02-17]
OMIM:231550	Achalasia-Addisonianism-Alacrima syndrome		HP:0000522	OMIM:231550;PMID:11062474	PCS		27/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10];HPO:probinson[2012-04-11]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001298	OMIM:246900	TAS				HP:0025303	P	HPO:skoehler[2013-06-06]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001254	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0000252	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001410	OMIM:246900	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001993	PMID:8506365	PCS		1/1			P	HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001332	PMID:8506365	PCS		1/1			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0003542	PMID:8506365	PCS		1/1			P	HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0011968	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001250	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001263	OMIM:246900	TAS		HP:0040281			P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001252	PMID:8506365	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001251	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0002240	OMIM:246900	TAS		HP:0040283			P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0003593	PMID:8506365	PCS		1/1			C	HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0500191	PMID:8506365	PCS		1/1			P	HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0003819	PMID:8506365	PCS		1/1			C	HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001639	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0500193	PMID:8506365	PCS		1/1			P	HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0000007	PMID:8506365	PCS					I	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001943	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0002910	PMID:8506365	PCS		1/1			P	HPO:skoehler[2013-04-02];HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0500187	PMID:8506365	PCS		1/1			P	HPO:probinson[2022-12-03]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0001942	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:246900	Dihydrolipoamide dehydrogenase deficiency		HP:0003128	OMIM:246900	TAS					P	HPO:skoehler[2013-04-02]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0000011	OMIM:263570	IEA					P	HPO:iea[2009-02-17]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0003477	OMIM:263570	TAS					P	HPO:skoehler[2017-07-13]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0003401	PMID:9851430	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0001278	OMIM:263570	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0003596	PMID:9851430	PCS		7/7			C	HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0001288	PMID:9851430	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0003394	PMID:9851430	PCS		1/7			P	HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0000020	PMID:9851430	PCS		7/7			P	HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0002273	OMIM:263570	TAS					P	HPO:skoehler[2010-06-20]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0100543	PMID:9851430	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0000007	PMID:9851430	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0002936	PMID:9851430	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0002922	PMID:9851430	PCS		2/7			P	HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0001258	PMID:9851430	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0003438	PMID:9851430	PCS		6/7			P	HPO:probinson[2022-11-08]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0002500	OMIM:263570	IEA					P	HPO:iea[2009-02-17]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0003677	OMIM:263570	IEA					C	HPO:iea[2009-02-17]
OMIM:263570	Polyglucosan body neuropathy, adult form		HP:0002127	OMIM:263570	IEA					P	HPO:iea[2009-02-17]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0002960	PMID:26783323	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0000100	PMID:26783323	PCS	HP:0003593	1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0012476	PMID:26783323	PCS		1/1			P	HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0002583	PMID:26783323	PCS	HP:0011463	1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0003593	PMID:26783323	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0033221	PMID:26783323	IEA		2/2			P	HPO:probinson[2020-12-07]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0031540	PMID:26783323	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0000007	PMID:26783323	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0031266	PMID:26783323	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0000093	PMID:26783323	PCS	HP:0003593	2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0003347	PMID:26783323	PCS		2/2			P	HPO:probinson[2020-10-19]
OMIM:617006	Autoimmune disease, multisystem, infantile-onset, 2		HP:0012579	PMID:26783323	PCS	HP:0003593	1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-19]
OMIM:203290	Albinism, oculocutaneous, type III		HP:0001022	OMIM:203290	IEA					P	HPO:skoehler[2015-01-27]
OMIM:203290	Albinism, oculocutaneous, type III		HP:0000486	OMIM:203290	IEA					P	HPO:iea[2009-02-17]
OMIM:203290	Albinism, oculocutaneous, type III		HP:0000639	OMIM:203290	TAS					P	HPO:probinson[2009-02-17]
OMIM:203290	Albinism, oculocutaneous, type III		HP:0002297	OMIM:203290	IEA					P	HPO:skoehler[2010-06-20]
OMIM:203290	Albinism, oculocutaneous, type III		HP:0000007	OMIM:203290	IEA					I	HPO:skoehler[2010-06-19]
OMIM:203290	Albinism, oculocutaneous, type III		HP:0007443	OMIM:203290	IEA					P	HPO:iea[2009-02-17]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001254	PMID:30576410	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001298	PMID:30576410	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002521	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001332	PMID:30576410	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001250	PMID:30576410	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002066	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0003593	PMID:30576410	PCS		3/6			C	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001251	PMID:30576410	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002180	PMID:30576410	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0010783	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002181	PMID:30576410	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0012469	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000518	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000737	PMID:30576410	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0011463	PMID:30576410	PCS		3/6			C	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000718	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002119	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001649	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0007325	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001644	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002014	PMID:30576410	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0008936	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002510	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002059	PMID:30576410	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000750	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0008619	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002013	PMID:30576410	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002376	PMID:30576410	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002572	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002371	PMID:30576410	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002151	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001263	PMID:30576410	PCS		2/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002171	PMID:30576410	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002072	PMID:30576410	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000708	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0003819	PMID:30576410	PCS		6/6			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0008066	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000602	PMID:30576410	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001954	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001712	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000007	PMID:30576410	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0000988	PMID:30576410	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002307	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001876	PMID:30576410	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0002500	PMID:30576410	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-04]
OMIM:618321	Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2		HP:0001336	PMID:30576410	PCS		1/6			P	HPO:probinson[2022-09-04]
OMIM:122580	Costocoracoid ligament, congenitally short		HP:0000782	OMIM:122580	IEA					P	HPO:skoehler[2009-02-17]
OMIM:122580	Costocoracoid ligament, congenitally short		HP:0200021	OMIM:122580	IEA					P	HPO:skoehler[2009-02-17]
OMIM:122580	Costocoracoid ligament, congenitally short		HP:0000006	OMIM:122580	IEA					I	HPO:iea[2009-02-17]
OMIM:122580	Costocoracoid ligament, congenitally short		HP:0001435	OMIM:122580	IEA					P	HPO:skoehler[2009-02-17]
OMIM:102650	Adactylia, unilateral		HP:0001597	OMIM:102650	IEA					P	HPO:iea[2009-02-17]
OMIM:102650	Adactylia, unilateral		HP:0009776	OMIM:102650	TAS				HP:0012833	P	HPO:iea[2009-02-17]
OMIM:102650	Adactylia, unilateral		HP:0009778	OMIM:102650	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:102650	Adactylia, unilateral		HP:0000006	OMIM:102650	IEA					I	HPO:iea[2009-02-17]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0009183	OMIM:186550	IEA					P	HPO:iea[2009-02-17]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0003016	OMIM:186550	TAS					P	HPO:iea[2013-03-30]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0001156	OMIM:186550	IEA					P	HPO:iea[2009-02-17]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0001233	OMIM:186550	IEA					P	HPO:iea[2009-02-17]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0001191	OMIM:186550	TAS					P	HPO:skoehler[2010-06-18]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0002987	OMIM:186550	IEA					P	HPO:iea[2009-02-17]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0000006	OMIM:186550	IEA					I	HPO:iea[2009-02-17]
OMIM:186550	Synostosis, carpal, with dysplastic elbow joints and brachydactyly		HP:0006190	OMIM:186550	IEA					P	HPO:iea[2009-02-17]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0003126	PMID:24401050	PCS					P	HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0003355	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0004322	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0000083	PMID:24401050	PCS		0/11			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0003076	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0003593	PMID:24401050	PCS					C	HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0002979	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0002748	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0003109	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0001510	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0000006	PMID:24401050	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0001942	PMID:24401050	PCS					P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-29]
OMIM:615605	Fanconi renotubular syndrome 3		HP:0003259	PMID:24401050	PCS		0/11			P	HPO:probinson[2022-09-29]
OMIM:615163	Cone-Rod dystrophy 17		HP:0000613	OMIM:615163	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615163	Cone-Rod dystrophy 17		HP:0000505	OMIM:615163	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615163	Cone-Rod dystrophy 17		HP:0000603	OMIM:615163	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615163	Cone-Rod dystrophy 17		HP:0000548	OMIM:615163	IEA					P	HPO:skoehler[2015-01-19]
OMIM:615163	Cone-Rod dystrophy 17		HP:0000543	OMIM:615163	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615163	Cone-Rod dystrophy 17		HP:0000006	OMIM:615163	TAS					I	HPO:skoehler[2013-05-07]
OMIM:618447	Long QT syndrome 8		HP:0003621	PMID:24728418	PCS		5/7			C	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0001663	PMID:24728418	PCS		1/7			P	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0031628	PMID:23677916	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0003581	PMID:24728418	PCS		2/7			C	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0005184	PMID:23677916;PMID:24728418	PCS		15/15			P	HPO:probinson[2022-02-27];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0001159	PMID:23677916;PMID:24728418	PCS		0/15			P	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0001279	PMID:23677916;PMID:24728418	PCS		4/15			P	HPO:probinson[2022-02-27];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0000006	PMID:23677916	PCS					I	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0001645	PMID:23677916	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0001249	PMID:23677916	PCS		0/8			P	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0001688	PMID:23677916	PCS		1/8			P	HPO:probinson[2022-02-27]
OMIM:618447	Long QT syndrome 8		HP:0002721	PMID:24728418	PCS		0/7			P	HPO:probinson[2022-02-27]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002014	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002378	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0003621	PMID:14976160	PCS		2/3			C	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0000970	PMID:14976160	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002661	PMID:14976160	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002495	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0010829	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0000020	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0003593	OMIM:608654	IEA					C	HPO:iea[2009-02-17]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0003040	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0003095	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0011463	PMID:14976160	PCS		1/3			C	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0007021	PMID:14976160	PCS		3/3		HP:0012839	P	HPO:skoehler[2013-06-06];HP:probinson[2018-07-14];HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0006121	PMID:3472625	PCS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0003419	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0009830	PMID:14976160	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0000007	PMID:14976160	PCS					I	HPO:iea[2009-02-17];HP:probinson[2018-07-14]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0001954	OMIM:608654	IEA		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002757	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002758	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002019	PMID:14976160	PCS		1/3			P	HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0007328	PMID:14976160	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-11]
OMIM:608654	Neuropathy, hereditary sensory and autonomic, type V		HP:0002754	PMID:14976160	PCS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000154	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0003577	PMID:28150392	PCS		1/1			C	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000175	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000494	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000252	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000365	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000007	PMID:28150392	PCS					I	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000568	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000414	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0030084	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0001873	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000201	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000278	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0000413	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619981	Braddock-Carey syndrome 2		HP:0005548	PMID:28150392	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0002553	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0003202	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000154	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000582	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0003577	PMID:31804630	PCS		1/1			C	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0001344	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000750	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0004322	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0001252	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0001263	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0005280	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000729	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000629	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000316	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000657	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0002714	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000565	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000322	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0001510	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0001763	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000047	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0000006	PMID:31804630	PCS					I	HPO:probinson[2022-04-17]
OMIM:619759	Tessadori-van Haaften neurodevelopmental syndrome 2		HP:0001249	PMID:31804630	PCS		1/1			P	HPO:probinson[2022-04-17]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0003577	OMIM:616481	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0002257	PMID:26073779	PCS		5/5			P	HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0001696	PMID:26073779	PCS		0/5			P	HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0002110	PMID:26073779	PCS		5/5			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0033036	PMID:26073779	PCS		3/3			P	HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0011109	PMID:26073779	PCS		5/5			P	HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0012265	PMID:26073779	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0012267	PMID:26073779	PCS					P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0012263	PMID:26073779	PCS					P	HPO:skoehler[2015-08-02];HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0000789	PMID:26073779	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0000007	PMID:26073779	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0000403	PMID:26073779	PCS		5/5			P	HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0006510	PMID:26073779	PCS		1/5			P	HPO:probinson[2022-10-11]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0002205	OMIM:616481	TAS					P	HPO:skoehler[2015-08-02]
OMIM:616481	Ciliary dyskinesia, primary, 32		HP:0002643	PMID:26073779	PCS		3/5			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-10-11]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0002037	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0003621	PMID:35007328	PCS		2/3			C	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0000750	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0001272	PMID:35007328	PCS		0/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0002043	PMID:35007328	PCS		2/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0003221	PMID:35007328	PCS		0/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0003593	PMID:35007328	PCS		1/3			C	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0033256	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0010976	PMID:35007328	PCS		3/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0002209	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0000007	PMID:35007328	PCS					I	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0000601	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0000967	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0005528	PMID:35007328	PCS		3/3			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0001511	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0008404	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0002745	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0001876	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0002721	PMID:35007328	PCS		3/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0001622	PMID:35007328	PCS		1/3			P	HPO:probinson[2023-01-19]
OMIM:620133	Dyskeratosis congenita, autosomal recessive 8		HP:0040218	PMID:35007328	PCS		3/3			P	HPO:probinson[2023-01-19]
OMIM:304500	Deafness, X-linked 1		HP:0000407	PMID:20021999	PCS	HP:0003577				P	HPO:iea[2014-05-24]
OMIM:304500	Deafness, X-linked 1		HP:0001419	PMID:20021999	PCS					I	HPO:iea[2014-05-24]
OMIM:614296	Wolfram-Like syndrome, autosomal dominant		HP:0003621	PMID:16648378;PMID:20069065	PCS		6/7			C	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-Like syndrome, autosomal dominant		HP:0030644	PMID:20069065	PCS		3/3			P	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000365	PMID:16648378	PCS		3/3			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0001141	PMID:18544103	PCS		1/2			P	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0040270	PMID:16648378	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000819	PMID:16648378	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000709	PMID:20069065	PCS		0/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0100753	PMID:20069065	PCS		0/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000738	PMID:20069065	PCS		0/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000716	OMIM:614296	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614296	Wolfram-Like syndrome, autosomal dominant		HP:0011463	PMID:16648378	PCS		1/4			C	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000407	PMID:20069065;PMID:18544103	PCS		4/5			P	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000739	PMID:16648378	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000717	PMID:20069065	PCS		0/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-Like syndrome, autosomal dominant		HP:0007663	PMID:16648378	PCS		4/4			P	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000648	PMID:16648378;PMID:18544103	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-07];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-Like syndrome, autosomal dominant		HP:0000543	PMID:16648378	PCS		3/4			P	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0001730	PMID:18544103	PCS		1/2			P	HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0005978	PMID:20069065;PMID:18544103	PCS		2/5			P	HPO:probinson[2022-05-07];HPO:probinson[2022-05-07];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000006	PMID:16648378	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-07]
OMIM:614296	Wolfram-like syndrome, autosomal dominant		HP:0000501	OMIM:614296	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:615188	Cataract, multiple types		HP:0003577	PMID:23288985	PCS		7/7			C	HPO:probinson[2023-01-21]
OMIM:615188	Cataract, multiple types		HP:0001134	PMID:23288985	PCS		2/7			P	HPO:probinson[2023-01-21]
OMIM:615188	Cataract, multiple types		HP:0000519	PMID:23288985	PCS		7/7			P	HPO:skoehler[2013-06-05];HPO:probinson[2023-01-21]
OMIM:615188	Cataract, multiple types		HP:0007971	PMID:23288985	PCS		4/7			P	HPO:probinson[2023-01-21]
OMIM:615188	Cataract, multiple types		HP:0000006	PMID:23288985	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2023-01-21]
OMIM:620655	Alfadhel syndrome		HP:0002069	PMID:32431071	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0002188	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0004322	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001250	PMID:32431071	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000085	PMID:32431071	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0003593	PMID:32431071	PCS		3/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0010863	PMID:32431071	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001270	PMID:33875846;PMID:32431071	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000319	PMID:32431071	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000718	PMID:32431071	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000316	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000414	PMID:32431071	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000278	PMID:32431071	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001249	PMID:32431071	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0003623	PMID:32431071	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0008936	PMID:33875846;PMID:32431071	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0002553	PMID:33875846;PMID:32431071	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001265	PMID:32431071	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000252	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0030863	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000233	PMID:32431071	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0002474	PMID:32431071	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001762	PMID:32431071	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001382	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001263	PMID:33875846;PMID:32431071	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000348	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000007	PMID:32431071	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0001258	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000322	PMID:32431071	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000369	PMID:33875846	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620655	Alfadhel syndrome		HP:0000325	PMID:32431071	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300000	Opitz GBBB syndrome		HP:0003577	PMID:15121778	PCS		7/7			C	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0002023	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0000023	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000463	PMID:15121778	PCS		17/44			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000260	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001274	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0002020	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0100333	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001629	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000319	PMID:15121778	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0011220	PMID:15121778	PCS		1/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001609	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000316	PMID:15121778	PCS		42/44			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0008751	PMID:15121778	PCS		2/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000219	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0000218	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0002835	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0006315	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000358	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001320	PMID:15121778	PCS		3/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000076	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000054	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000252	PMID:15121778	PCS		2/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0002015	PMID:15121778	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000175	PMID:15121778	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000431	PMID:15121778	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0010957	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001263	PMID:15121778	PCS		19/37			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001739	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0001419	PMID:15121778	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000506	PMID:15121778	PCS		37/37			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000349	PMID:15121778	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001537	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0006783	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0002007	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0000047	PMID:15121778	PCS		37/44			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0001510	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0025407	PMID:15121778	PCS		1/7			P	HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000369	PMID:15121778	PCS		2/7			P	HPO:probinson[2022-04-28];HPO:probinson[2022-04-28]
OMIM:300000	Opitz GBBB syndrome		HP:0000028	OMIM:300000	IEA					P	HPO:iea[2009-02-17]
OMIM:300000	Opitz GBBB syndrome		HP:0000204	PMID:15121778	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-28]
OMIM:160980	Carney complex, type 1		HP:0003764	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0006769	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0001003	PMID:10973256	PCS		7/10			P	HPO:probinson[2021-05-08]
OMIM:160980	Carney complex, type 1		HP:0002893	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0005587	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0002890	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0001480	OMIM:160980	TAS					P	HPO:skoehler[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0002297	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0034941	PMID:33089457	PCS		1/1			P	HPO:probinson[2023-07-18];HPO:probinson[2023-07-18]
OMIM:160980	Carney complex, type 1		HP:0011672	PMID:10973256	PCS		5/10			P	HPO:probinson[2021-05-08]
OMIM:160980	Carney complex, type 1		HP:0100008	OMIM:160980	TAS					P	HPO:skoehler[2012-10-17]
OMIM:160980	Carney complex, type 1		HP:0033794	PMID:10973256	PCS		6/10			P	HPO:probinson[2021-05-08]
OMIM:160980	Carney complex, type 1		HP:0001635	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0000845	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0008225	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0007832	OMIM:160980	TAS					P	HPO:probinson[2022-07-01]
OMIM:160980	Carney complex, type 1		HP:0000006	PMID:10973256	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-08]
OMIM:160980	Carney complex, type 1		HP:0001007	OMIM:160980	TAS					P	HPO:skoehler[2009-02-17]
OMIM:160980	Carney complex, type 1		HP:0002666	OMIM:160980	IEA					P	HPO:iea[2009-02-17]
OMIM:137600	Iridogoniodysgenesis, type 2		HP:0000164	PMID:9618168	PCS		HP:0040281			P	HPO:curators[2012-04-19]
OMIM:137600	Iridogoniodysgenesis, type 2		HP:0007990	PMID:9618168;PMID:5804028	PCS		HP:0040281			P	HPO:curators[2009-02-17]
OMIM:137600	Iridogoniodysgenesis, type 2		HP:0001999	PMID:9618168;PMID:8942889	PCS					P	HPO:curators[2012-04-19]
OMIM:137600	Iridogoniodysgenesis, type 2		HP:0007730	PMID:9618168;PMID:5804028	PCS		HP:0040281			P	HPO:curators[2012-04-19]
OMIM:137600	Iridogoniodysgenesis, type 2		HP:0000006	PMID:9618168;PMID:5804028	PCS					I	HPO:curators[2009-02-17]
OMIM:137600	Iridogoniodysgenesis, type 2		HP:0000501	PMID:9618168;PMID:6881141	PCS		HP:0040281			P	HPO:curators[2009-02-17]
OMIM:620641	Tan-Almurshedi syndrome		HP:0003577	PMID:37179472	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0001250	PMID:37179472	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0001890	PMID:37179472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0012745	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0010764	PMID:37179472	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0010702	PMID:37179472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0001508	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000958	PMID:37179472	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0002719	PMID:37179472	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0011220	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0003508	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000358	PMID:37179472	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000252	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000431	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0001762	PMID:37179472	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000232	PMID:37179472	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0002475	PMID:37179472	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0012758	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0012385	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0009891	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000964	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000007	PMID:37179472	PCS					I	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0001511	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0001257	PMID:37179472	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000248	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000369	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620641	Tan-Almurshedi syndrome		HP:0000687	PMID:37179472	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0000550	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:6000571	PMID:37922835	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0002059	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0000750	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0001311	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0002376	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0001250	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0003463	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0002074	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0001251	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0000529	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0000007	OMIM:204500	IEA					I	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0000546	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0001336	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:204500	Ceroid lipofuscinosis, neuronal, 2		HP:0003205	OMIM:204500	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000561	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0002983	OMIM:256520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001770	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000518	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001848	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000316	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0003826	OMIM:256520	IEA					C	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0100807	PMID:24836451	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0009466	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001643	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0002414	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0007525	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000175	PMID:24836451	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0002190	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0012385	OMIM:256520	TAS					P	HPO:skoehler[2013-10-22]
OMIM:256520	Neu-Laxova syndrome 1		HP:0011451	PMID:24836451	PCS		3/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0007430	PMID:24836451	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001339	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000007	PMID:24836451	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0006101	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000568	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0006266	OMIM:256520	TAS					P	HPO:skoehler[2014-07-11]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000400	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000520	PMID:24836451	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001059	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000204	PMID:24836451	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000369	PMID:24836451	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001655	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000445	PMID:24836451	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0003577	PMID:24836451	PCS		3/3			C	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000340	PMID:24836451	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0002089	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001274	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001196	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0031244	PMID:24836451	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0012444	PMID:24836451	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001629	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001669	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001305	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0002119	PMID:24836451	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0030084	OMIM:256520	TAS					P	HPO:skoehler[2014-09-21]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001989	PMID:24836451	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000136	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000179	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000457	PMID:24836451	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0009826	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001561	PMID:24836451	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000475	PMID:24836451	PCS		1/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001321	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000470	PMID:24836451	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0011224	PMID:24836451	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0008064	PMID:24836451	PCS		2/3			P	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001838	PMID:24836451	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0009473	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001558	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0001511	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0003811	PMID:24836451	PCS		1/3			C	HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000028	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0002324	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000347	PMID:24836451	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-23]
OMIM:256520	Neu-Laxova syndrome 1		HP:0000104	OMIM:256520	IEA					P	HPO:iea[2009-02-17]
OMIM:603098	Deafness, autosomal recessive 13		HP:0000365	PMID:9781028	TAS					P	HPO:lccarmody[2019-01-29]
OMIM:603098	Deafness, autosomal recessive 13		HP:0000407	PMID:9781028	TAS					P	HPO:lccarmody[2019-01-29]
OMIM:603098	Deafness, autosomal recessive 13		HP:0000007	OMIM:603098	TAS					I	HPO:skoehler[2017-07-13]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0002861	OMIM:249400	IEA					P	HPO:iea[2009-02-17]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0006824	OMIM:249400	IEA					P	HPO:iea[2009-02-17]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0001442	PMID:23392294	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-07-20]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0001250	OMIM:249400	IEA					P	HPO:iea[2009-02-17]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0003396	OMIM:249400	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0001263	OMIM:249400	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0100702	OMIM:249400	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0002858	OMIM:249400	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0001305	OMIM:249400	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0000238	OMIM:249400	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0003745	OMIM:249400	IEA					I	HPO:iea[2009-02-17]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0001522	OMIM:249400	IEA					C	HPO:iea[2009-02-17]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0200022	OMIM:249400	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0001268	OMIM:249400	IEA					P	HPO:iea[2009-02-17]
OMIM:249400	Neurocutaneous melanosis, somatic		HP:0005603	OMIM:249400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604091	HDL deficiency, familial, 1		HP:0003233	PMID:30503498	PCS		6/7			P	HPO:probinson[2013-12-15];HPO:probinson[2024-03-10]
OMIM:604091	HDL deficiency, familial, 1		HP:0002155	PMID:30503498	PCS		0/7			P	HPO:lccarmody[2018-10-04];HPO:probinson[2024-03-10]
OMIM:604091	HDL deficiency, familial, 1		HP:0001658	PMID:10431236	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:604091	HDL deficiency, familial, 1		HP:0005181	PMID:7627690	PCS		2/4			P	HPO:lccarmody[2018-10-04];HPO:lccarmody[2018-10-04]
OMIM:604091	HDL deficiency, familial, 1		HP:0000006	PMID:9888879	PCS					I	HPO:probinson[2013-12-15]
OMIM:180860	Silver-Russell syndrome 1		HP:0004220	OMIM:180860	TAS					P	HPO:probinson[2012-06-09]
OMIM:180860	Silver-Russell syndrome 1		HP:0000957	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0001626	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0030062	OMIM:180860	TAS					P	HPO:skoehler[2014-09-21]
OMIM:180860	Silver-Russell syndrome 1		HP:0002714	OMIM:180860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0003745	OMIM:180860	IEA					I	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0001402	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0010957	OMIM:180860	TAS					P	HPO:skoehler[2013-05-31]
OMIM:180860	Silver-Russell syndrome 1		HP:0002750	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0000270	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0000592	OMIM:180860	TAS					P	HPO:probinson[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0001263	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0005461	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0003162	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0010481	OMIM:180860	IEA					P	HPO:skoehler[2010-06-20]
OMIM:180860	Silver-Russell syndrome 1		HP:0001518	OMIM:180860	TAS					P	HPO:probinson[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0000824	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0100617	OMIM:180860	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0004209	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0002007	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0001511	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0002667	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0001159	OMIM:180860	IEA					P	HPO:skoehler[2010-06-20]
OMIM:180860	Silver-Russell syndrome 1		HP:0000069	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0000047	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0000006	OMIM:180860	IEA					I	HPO:skoehler[2019-04-18]
OMIM:180860	Silver-Russell syndrome 1		HP:0000347	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0000325	OMIM:180860	IEA					P	HPO:iea[2009-02-17]
OMIM:180860	Silver-Russell syndrome 1		HP:0004227	OMIM:180860	TAS					P	HPO:probinson[2012-06-09]
OMIM:551000	Myopathy, mitochondrial, lethal infantile		HP:0003198	OMIM:551000	TAS					P	HPO:probinson[2009-02-17]
OMIM:551000	Myopathy, mitochondrial, lethal infantile		HP:0009069	OMIM:551000	TAS					P	HPO:probinson[2009-02-17]
OMIM:551000	Myopathy, mitochondrial, lethal infantile		HP:0001427	OMIM:551000	TAS					I	HPO:probinson[2012-07-18]
OMIM:551000	Myopathy, mitochondrial, lethal infantile		HP:0003128	OMIM:551000	TAS					P	HPO:probinson[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0003202	OMIM:607598	TAS					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0001561	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0011003	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0000969	OMIM:607598	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0001629	OMIM:607598	TAS		HP:0040283			P	HPO:probinson[2012-04-25]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0000007	OMIM:607598	IEA					I	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0001558	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0002804	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0002878	OMIM:607598	TAS	HP:0003593				P	HPO:probinson[2014-05-29]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0002304	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0007964	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0000347	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0000126	OMIM:607598	IEA					P	HPO:iea[2009-02-17]
OMIM:607598	Lethal congenital contracture syndrome 2		HP:0001644	OMIM:607598	TAS		HP:0040283			P	HPO:probinson[2012-04-25]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0000154	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0006956	PMID:24817631	PCS		1/1			P	HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0000054	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0001344	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0000750	PMID:24817631	PCS		1/1			P	HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0004279	PMID:24817631	PCS		1/1			P	HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0000463	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0031936	PMID:24817631	PCS		1/1			P	HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0001250	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0001263	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0000280	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0001419	PMID:25644381	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0008689	PMID:24817631	PCS		1/1			P	HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0001249	PMID:25644381	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300982	Intellectual developmental disorder, X-linked 103		HP:0002126	PMID:24817631	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0011939	PMID:15805154	PCS		1/5			P	HPO:probinson[2024-07-22]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0003577	PMID:15805154	PCS		5/5			C	HPO:probinson[2022-11-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0001233	PMID:15805154	PCS		1/5			P	HPO:probinson[2022-11-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0010709	PMID:15805154	PCS		1/5			P	HPO:probinson[2022-11-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0000691	OMIM:225280	IEA					P	HPO:iea[2009-02-17]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0001592	OMIM:225280	IEA					P	HPO:iea[2009-02-17]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0010707	PMID:15805154	PCS		1/5			P	HPO:probinson[2022-11-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0001171	PMID:15805154	PCS	HP:0003577	1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0045075	OMIM:225280	TAS					P	HPO:probinson[2022-05-07]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0012385	OMIM:225280	TAS					P	HPO:skoehler[2013-10-22]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0000968	OMIM:225280	IEA					P	HPO:skoehler[2015-01-14]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0009473	OMIM:225280	IEA					P	HPO:iea[2009-02-17]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0002209	OMIM:225280	IEA					P	HPO:iea[2009-02-17]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0000007	PMID:15805154	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0000975	PMID:15805154	PCS		0/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0007754	OMIM:225280	IEA					P	HPO:iea[2009-02-17]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0000653	OMIM:225280	IEA					P	HPO:iea[2009-02-17]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0009779	PMID:15805154	PCS		1/5			P	HPO:probinson[2022-11-08];HPO:probinson[2022-11-08]
OMIM:225280	Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome		HP:0000687	OMIM:225280	IEA					P	HPO:iea[2009-02-17]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0002267	PMID:37660254	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0003577	PMID:37660254	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001310	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001332	PMID:37660254	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001272	PMID:37660254	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001250	PMID:37660254	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001251	PMID:37660254	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0003593	PMID:37660254	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0002180	PMID:37660254	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0033725	PMID:37660254	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001508	PMID:37660254	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0100704	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0011463	PMID:37660254	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0025336	PMID:37660254	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001268	PMID:37660254	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001347	PMID:37660254	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0003623	PMID:37660254	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0002454	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0008936	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0002015	PMID:37660254	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0000252	PMID:37660254	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0003621	PMID:37660254	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0000750	PMID:37660254	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001344	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0031936	PMID:37660254	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001321	PMID:37660254	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0011968	PMID:37660254	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001260	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001263	PMID:37660254	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0040130	PMID:37660254	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0012675	PMID:37660254	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0012343	PMID:37660254	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0012464	PMID:37660254	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0034295	PMID:37660254	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0041056	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0001257	PMID:37660254	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0002305	PMID:37660254	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620669	Neurodegeneration with brain iron accumulation 9		HP:0000006	PMID:37660254	PCS					I	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:262875	Platelet prostacyclin receptor defect		HP:0001939	OMIM:262875	IEA					P	HPO:iea[2009-02-17]
OMIM:262875	Platelet prostacyclin receptor defect		HP:0000007	OMIM:262875	IEA					I	HPO:iea[2009-02-17]
OMIM:262875	Platelet prostacyclin receptor defect		HP:0004417	OMIM:262875	IEA					P	HPO:iea[2009-02-17]
OMIM:276800	TYROSINOSIS		HP:0003231	OMIM:276800	IEA					P	HPO:iea[2009-02-17]
OMIM:276800	TYROSINOSIS		HP:0000007	OMIM:276800	IEA					I	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001254	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001397	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0008309	OMIM:201450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0002013	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0003234	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001250	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:6000356	PMID:2393404	PCS		3/3			P	HPO:probinson[2024-02-27]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001252	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001263	OMIM:201450	TAS					P	HPO:probinson[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0002240	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001290	OMIM:201450	TAS					P	HPO:skoehler[2017-07-13]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0002181	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:6000605	PMID:6402754	PCS		2/2			P	HPO:probinson[2024-04-03]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0000007	OMIM:201450	IEA					I	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001943	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0002910	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0003108	OMIM:201450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001942	OMIM:201450	TAS		20/20		HP:0012825	P	HPO:probinson[2012-05-05];HPO:iea[2009-02-17]
OMIM:201450	Acyl-Coa dehydrogenase, medium-chain, deficiency of		HP:0001259	OMIM:201450	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000286	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000100	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000463	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001250	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0002286	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001010	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001252	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0002240	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0002680	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001290	OMIM:269920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:269920	Infantile sialic acid storage disease		HP:0000280	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000639	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001508	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000938	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001922	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000238	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001789	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000218	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000212	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001744	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001622	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001760	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0002059	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001541	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001640	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0003025	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001263	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0002908	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0003819	OMIM:269920	IEA					C	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000508	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000007	OMIM:269920	IEA					I	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0001635	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:269920	Infantile sialic acid storage disease		HP:0000765	OMIM:269920	IEA					P	HPO:iea[2009-02-17]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0003676	PMID:19542096	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0000486	PMID:27782104	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0000540	PMID:27782104	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001371	OMIM:618484	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001252	PMID:19542096	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001290	OMIM:618484	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0003391	OMIM:618484	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0012785	PMID:27782104	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0030319	PMID:19542096	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0100297	PMID:19542096	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0040081	PMID:19542096	PCS		0/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0011461	PMID:19542096;PMID:27782104	PCS		3/3			C	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0003701	PMID:27782104	PCS		1/1			P	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001265	PMID:27782104	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0002751	PMID:19542096	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0003687	PMID:19542096;PMID:27782104	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0002650	PMID:19542096	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001762	PMID:19542096	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0031936	PMID:19542096	PCS		2/2			P	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001284	PMID:19542096	PCS		1/2			P	HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0002194	PMID:19542096	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001181	PMID:27782104	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0002091	PMID:19542096	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0002808	OMIM:618484	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001518	PMID:19542096;PMID:27782104	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0002804	PMID:19542096;PMID:27782104	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0000007	PMID:19542096	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001558	PMID:19542096;PMID:27782104	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0000028	PMID:27782104	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0001776	PMID:19542096	PCS		2/2			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:618484	Arthrogryposis multiplex congenita 3, myogenic type		HP:0003557	PMID:19542096;PMID:27782104	PCS		2/3			P	HPO:probinson[2022-08-27]
OMIM:260910	Perifolliculitis capitis abscedens et suffodiens, familial		HP:0001596	OMIM:260910	IEA					P	HPO:skoehler[2010-06-20]
OMIM:260910	Perifolliculitis capitis abscedens et suffodiens, familial		HP:0012322	OMIM:260910	IEA					P	HPO:skoehler[2015-01-27]
OMIM:260910	Perifolliculitis capitis abscedens et suffodiens, familial		HP:0002293	OMIM:260910	IEA					P	HPO:skoehler[2015-04-18]
OMIM:260910	Perifolliculitis capitis abscedens et suffodiens, familial		HP:0003745	OMIM:260910	TAS					I	HPO:iea[2009-02-17]
OMIM:258900	Orotic aciduria		HP:0003267	OMIM:258900	IEA					P	HPO:iea[2009-02-17]
OMIM:258900	Orotic aciduria		HP:0001263	OMIM:258900	TAS		HP:0040283			P	HPO:probinson[2012-06-03]
OMIM:258900	Orotic aciduria		HP:0000790	OMIM:258900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:258900	Orotic aciduria		HP:0011840	OMIM:258900	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:258900	Orotic aciduria		HP:0011273	OMIM:258900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:258900	Orotic aciduria		HP:0001629	OMIM:258900	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:258900	Orotic aciduria		HP:0001508	PMID:9042911	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-06]
OMIM:258900	Orotic aciduria		HP:0032231	OMIM:258900	IEA					P	HPO:skoehler[2019-02-22]
OMIM:258900	Orotic aciduria		HP:0000007	PMID:9042911	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:258900	Orotic aciduria		HP:0004826	OMIM:258900	IEA					P	HPO:iea[2009-02-17]
OMIM:258900	Orotic aciduria		HP:0003218	PMID:9042911	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-06]
OMIM:258900	Orotic aciduria		HP:0003526	OMIM:258900	TAS					P	HPO:iea[2009-02-17]
OMIM:258900	Orotic aciduria		HP:0003339	OMIM:258900	TAS					P	HPO:iea[2012-06-03]
OMIM:258900	Orotic aciduria		HP:0001631	OMIM:258900	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:258900	Orotic aciduria		HP:0004447	OMIM:258900	TAS					P	HPO:skoehler[2012-10-17]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000286	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000483	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0010529	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000365	PMID:35977029;PMID:28258187	PCS		0/16			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0004322	PMID:35977029;PMID:28258187	PCS		6/18			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001250	PMID:35977029;PMID:28258187	PCS		6/20			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0025268	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001252	PMID:35977029;PMID:28258187	PCS		8/16			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0003393	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0012427	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000639	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000957	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0010055	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0011463	PMID:35977029;PMID:28258187	PCS		10/24			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000718	PMID:35977029;PMID:28258187	PCS		6/18			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000316	PMID:35977029;PMID:28258187	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000437	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001800	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000311	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001763	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001840	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001249	PMID:35977029;PMID:28258187	PCS		16/20			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000358	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0009901	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0002751	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001265	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000010	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001387	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0011968	PMID:35977029;PMID:28258187	PCS		16/22			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000490	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001263	PMID:35977029;PMID:28258187	PCS		12/16			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000294	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000729	PMID:35977029;PMID:28258187	PCS		6/10			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0011330	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000965	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000722	PMID:35977029;PMID:28258187	PCS		6/18			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0009656	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000565	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001337	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000006	PMID:35977029	PCS					I	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001792	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000582	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000343	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000540	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0010747	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001156	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0003097	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001270	PMID:35977029;PMID:28258187	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0012048	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0012368	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0034681	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001508	PMID:35977029;PMID:28258187	PCS		8/16			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000739	PMID:35977029;PMID:28258187	PCS		6/18			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0008551	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000733	PMID:35977029;PMID:28258187	PCS		6/18			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000337	PMID:35977029;PMID:28258187	PCS		6/6			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000414	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000219	PMID:35977029;PMID:28258187	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0030084	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000218	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000378	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001623	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0002236	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000577	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0003621	PMID:35977029;PMID:28258187	PCS		14/24			C	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000750	PMID:35977029;PMID:28258187	PCS		20/20			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000431	PMID:35977029;PMID:28258187	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0002376	PMID:35977029;PMID:28258187	PCS		2/20			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000276	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000232	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0002099	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0045025	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0010535	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0010780	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0100716	PMID:35977029;PMID:28258187	PCS		6/18			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000505	PMID:35977029;PMID:28258187	PCS		2/10			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0025700	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0002329	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001511	PMID:35977029;PMID:28258187	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000664	PMID:35977029;PMID:28258187	PCS		4/4			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0007018	PMID:35977029;PMID:28258187	PCS		6/18			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000303	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0000545	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0004469	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:620494	Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies		HP:0001831	PMID:35977029;PMID:28258187	PCS		2/2			P	ORCID:0000-0002-5648-2155[2024-04-01]
OMIM:215800	Cleft larynx, posteriorstridor, congenital, included		HP:0001608	OMIM:215800	IEA					P	HPO:iea[2009-02-17]
OMIM:215800	Cleft larynx, posteriorstridor, congenital, included		HP:0000007	OMIM:215800	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:215800	Cleft larynx, posteriorstridor, congenital, included		HP:0002835	OMIM:215800	IEA					P	HPO:iea[2009-02-17]
OMIM:215800	Cleft larynx, posteriorstridor, congenital, included		HP:0000961	OMIM:215800	IEA					P	HPO:iea[2009-02-17]
OMIM:215800	Cleft larynx, posteriorstridor, congenital, included		HP:0006511	OMIM:215800	IEA					P	HPO:iea[2009-02-17]
OMIM:617238	Myopia 25, autosomal dominant		HP:0003621	PMID:25741866	PCS		9/9			C	HPO:probinson[2023-02-20]
OMIM:617238	Myopia 25, autosomal dominant		HP:0000541	PMID:25741866	PCS	HP:0003584	1/9			P	HPO:probinson[2023-02-20]
OMIM:617238	Myopia 25, autosomal dominant		HP:0011003	PMID:25741866	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:617238	Myopia 25, autosomal dominant		HP:0000006	PMID:25741866	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-20]
OMIM:609006	Deafness, autosomal recessive 36, with or without vestibular involvement		HP:0000407	OMIM:609006	TAS	HP:0003593				P	HPO:probinson[2013-03-30]
OMIM:609006	Deafness, autosomal recessive 36, with or without vestibular involvement		HP:0000007	OMIM:609006	TAS					I	HPO:probinson[2013-01-09]
OMIM:609006	Deafness, autosomal recessive 36, with or without vestibular involvement		HP:0008568	OMIM:609006	TAS					P	HPO:probinson[2013-03-30]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0004322	OMIM:309583	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001250	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0003199	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001252	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001290	OMIM:309583	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0004283	OMIM:309583	TAS					P	HPO:probinson[2012-07-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0045075	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000319	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001609	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000316	OMIM:309583	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000954	PMID:19206178	PCS		1/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0100807	OMIM:309583	TAS					P	HPO:probinson[2012-07-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000678	PMID:19206178	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001847	PMID:19206178	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001249	PMID:19206178	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002751	PMID:19206178	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000175	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001187	OMIM:309583	TAS					P	HPO:probinson[2012-07-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000098	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001260	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001263	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0011003	OMIM:309583	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001419	PMID:19206178	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000767	PMID:19206178	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002705	PMID:19206178	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000768	OMIM:309583	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000322	OMIM:309583	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000248	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000324	PMID:19206178	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001611	PMID:19206178	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000463	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002684	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000939	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000414	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002757	PMID:19206178	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0006610	PMID:19206178	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002953	PMID:19206178	PCS		1/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000377	OMIM:309583	IEA					P	HPO:skoehler[2010-06-20]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000179	PMID:19206178	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002753	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002136	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0001762	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0002650	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000193	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000470	PMID:19206178	PCS		1/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0011302	OMIM:309583	TAS					P	HPO:probinson[2012-07-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000508	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000426	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000664	PMID:19206178	PCS		2/2			P	HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000465	PMID:19206178	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-10-15]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000028	OMIM:309583	IEA					P	HPO:iea[2009-02-17]
OMIM:309583	Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type		HP:0000303	OMIM:309583	IEA					P	HPO:skoehler[2010-06-18]
OMIM:619215	Oculomotor-abducens synkinesis		HP:0003577	PMID:31211835	PCS					C	HPO:probinson[2021-05-19]
OMIM:619215	Oculomotor-abducens synkinesis		HP:0000508	PMID:31211835	PCS	HP:0003577	4/5			P	HPO:probinson[2021-05-19]
OMIM:619215	Oculomotor-abducens synkinesis		HP:0033851	PMID:31211835	PCS		3/5			P	HPO:probinson[2021-06-13]
OMIM:619215	Oculomotor-abducens synkinesis		HP:0000007	PMID:31211835	PCS					I	HPO:probinson[2021-05-19];HPO:probinson[2021-05-19]
OMIM:619215	Oculomotor-abducens synkinesis		HP:0009921	PMID:31211835	PCS		1/5			P	HPO:probinson[2021-05-19]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0002135	PMID:25307056	IEA		3/3			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-26];HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0001250	PMID:25307056;PMID:22859821	PCS		3/6			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-26];HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0020086	PMID:22859821	PCS		3/3			P	HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0003593	PMID:22859821	PCS		1/1			C	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0034752	PMID:22859821	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0012759	PMID:22859821	PCS		0/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0031691	PMID:25307056	PCS		0/3			P	HP:probinson[2019-01-26];HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0034751	PMID:22859821	PCS		1/3			P	HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0011274	PMID:22859821	PCS		2/3			P	HPO:probinson[2015-02-25];HP:probinson[2019-01-26];HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0000007	PMID:22859821	PCS					I	HPO:probinson[2015-02-25];HP:probinson[2019-01-26]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0002716	PMID:22859821	PCS		2/3			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-26]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0004429	PMID:22859821	PCS		0/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2024-03-15]
OMIM:616126	Immunodeficiency 38 with basal ganglia calcification		HP:0002721	PMID:22859821	PCS					P	HPO:skoehler[2015-07-29];HPO:probinson[2024-03-15]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002582	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001890	PMID:32562707	PCS		1/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0003593	PMID:31308374	PCS		1/3			C	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0011463	PMID:32562707	PCS		1/4			C	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0011461	PMID:31308374	PCS		2/3			C	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0000316	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0100806	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001888	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0005208	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0000952	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001644	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0031956	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0000175	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002155	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001541	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0011968	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0030948	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0012189	PMID:32562707	PCS		1/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0033222	PMID:32562707	PCS		3/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0011131	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0000007	PMID:31308374	PCS					I	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002900	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001397	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001396	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002202	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001399	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0020072	PMID:32562707	PCS		3/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0025289	PMID:32562707	PCS		1/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002240	PMID:31308374	PCS		2/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0031964	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001709	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0031692	PMID:32562707	PCS		1/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002718	PMID:31308374	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0006695	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0012050	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001942	PMID:31308374	PCS		2/3			P	HP:probinson[2021-11-27];HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001788	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001562	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0003621	PMID:32562707	PCS		3/4			C	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0200128	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0003186	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002092	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0031378	PMID:32562707	PCS		1/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0011227	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0032229	PMID:32562707;PMID:31308374	PCS		2/7			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0033165	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0034056	PMID:31308374	PCS		1/1			P	HPO:probinson[2022-02-03]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001518	PMID:31308374	PCS		2/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0011473	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0000822	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001878	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001954	PMID:32562707	PCS		1/4			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0020136	PMID:31308374	PCS		1/3			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0004429	PMID:31308374	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001511	PMID:31308374	PCS		2/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001631	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001510	PMID:31308374	PCS		2/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0001873	PMID:31308374	PCS		1/3			P	HP:probinson[2021-11-27]
OMIM:619573	Immunodeficiency 87 and autoimmunity		HP:0002841	PMID:31308374	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0002300	OMIM:616640	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0002510	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0003676	OMIM:616640	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0002123	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0002497	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0001250	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0001260	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0000020	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0001251	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0002073	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0011999	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0000709	OMIM:616640	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0100543	OMIM:616640	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0100318	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0000738	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0000726	OMIM:616640	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0003828	OMIM:616640	TAS					M	HPO:skoehler[2017-07-13]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0000007	PMID:22961547	PCS					I	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0001257	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0001336	PMID:22961547	PCS					P	HPO:probinson[2017-06-17]
OMIM:616640	Epilepsy, progressive myoclonic, 10		HP:0001347	OMIM:616640	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0002553	OMIM:616898	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0010804	OMIM:616898	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0003577	PMID:17163532	PCS		1/1			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000175	PMID:17163532	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000232	OMIM:616898	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0001252	PMID:17163532	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0001263	PMID:17163532	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0410030	OMIM:616898	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0001629	OMIM:616898	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0033166	PMID:17163532	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000348	OMIM:616898	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000307	PMID:17163532	PCS		1/1			P	HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000322	PMID:17163532	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0001631	PMID:17163532	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000358	PMID:17163532	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000369	PMID:17163532	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0001249	OMIM:616898	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616898	Chromosome 15q14 deletion syndrome		HP:0000006	PMID:17163532	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-02]
OMIM:115660	Cataract 7		HP:0000572	OMIM:115660	IEA					P	HPO:skoehler[2010-06-20]
OMIM:115660	Cataract 7		HP:0000519	OMIM:115660	TAS					P	HPO:skoehler[2015-01-21]
OMIM:115660	Cataract 7		HP:0032037	OMIM:115660	IEA					P	HPO:skoehler[2019-02-22]
OMIM:115660	Cataract 7		HP:0000006	OMIM:115660	IEA					I	HPO:iea[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0002169	PMID:9585612	PCS		4/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0003577	PMID:9585612	PCS		7/17			C	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0003542	OMIM:266150	IEA					P	HPO:iea[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0001250	PMID:9585612	PCS		8/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0001263	PMID:9585612	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0001252	PMID:9585612	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0002151	OMIM:266150	IEA					P	HPO:iea[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0002240	OMIM:266150	IEA					P	HPO:iea[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0003593	PMID:9585612	PCS		10/17			C	HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0007190	OMIM:266150	TAS					P	HPO:skoehler[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0000007	PMID:9585612	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0001943	PMID:9585612	PCS		4/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0006970	OMIM:266150	IEA					P	HPO:iea[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0002415	OMIM:266150	IEA					P	HPO:skoehler[2018-10-08]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0002305	PMID:9585612	PCS		4/17			P	HPO:probinson[2022-11-02]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0001249	OMIM:266150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0002049	OMIM:266150	TAS					P	HPO:probinson[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0003348	OMIM:266150	IEA					P	HPO:iea[2009-02-17]
OMIM:266150	Pyruvate carboxylase deficiency		HP:0003128	PMID:9585612	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-02]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0004325	OMIM:615349	TAS					P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0010648	PMID:29931299	PCS		4/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0004322	PMID:29931299	PCS		10/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0430047	PMID:23664117	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001252	PMID:29931299;PMID:23664117	PCS		9/14			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-04];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0003593	PMID:29931299	PCS		10/10			C	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0010049	PMID:23664117	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0010646	PMID:29931299	PCS		3/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0011341	PMID:23664117	PCS		3/4			P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0011220	PMID:23664117	PCS		4/4			P	HPO:skoehler[2013-08-18];HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002616	PMID:29931299	PCS		3/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002659	PMID:29931299	PCS		8/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0009702	OMIM:615349;PMID:23664117	PCS		2/14			P	HPO:skoehler[2013-08-18];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002656	OMIM:615349	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002751	PMID:29931299;PMID:23664117	PCS		14/14			P	HPO:skoehler[2013-08-18];HPO:probinson[2023-02-04];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000175	OMIM:615349;PMID:23664117	PCS		3/14			P	HPO:skoehler[2013-08-18];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001385	PMID:29931299	PCS		4/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001222	PMID:23664117	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001382	PMID:29931299	PCS		10/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001263	PMID:29931299	PCS		5/10			P	HPO:skoehler[2013-08-18];HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0034392	PMID:29931299	PCS		10/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002827	PMID:23664117	PCS		3/4			P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000926	PMID:23664117	PCS		4/4			P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000767	OMIM:615349	TAS		HP:0040283			P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000007	PMID:29931299	PCS					I	HPO:skoehler[2013-08-18];HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002822	PMID:23664117	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000520	PMID:29931299;PMID:23664117	PCS		14/14			P	HPO:skoehler[2013-08-18];HPO:probinson[2023-02-04];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0004568	PMID:23664117	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0003015	PMID:23664117	PCS		3/4			P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001075	PMID:29931299	PCS		5/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001270	PMID:29931299	PCS		5/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0012368	PMID:29931299;PMID:23664117	PCS		14/14			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-02-04];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0008070	OMIM:615349	TAS					P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0006094	PMID:23664117	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000938	PMID:29931299	PCS		8/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000977	PMID:29931299	PCS		9/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001027	PMID:23664117	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000974	PMID:29931299;PMID:23664117	PCS		10/14			P	HPO:skoehler[2013-08-18];HPO:probinson[2023-02-04];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000973	PMID:29931299;PMID:23664117	PCS		8/14			P	HPO:skoehler[2013-08-18];HPO:probinson[2023-02-04];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002996	PMID:23664117	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0001762	PMID:23664117	PCS		2/4			P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0004233	PMID:23664117	PCS		1/4			P	HPO:skoehler[2013-08-18];HPO:probinson[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000592	PMID:23664117	PCS		3/4			P	HPO:skoehler[2013-08-18]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0010575	PMID:29931299;PMID:23664117	PCS		11/14			P	HPO:probinson[2023-02-04];ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002093	PMID:29931299	PCS		2/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000946	PMID:29931299	PCS		10/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0009473	PMID:23664117	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002209	PMID:23664117	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0006487	PMID:29931299	PCS		10/10			P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0002007	PMID:29931299	PCS					P	HPO:probinson[2023-02-04]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0008824	PMID:23664117	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:615349	Ehlers-Danlos syndrome, spondylodysplastic type, 2		HP:0000347	PMID:23664117	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-03]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0001892	OMIM:188025	IEA				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0000243	OMIM:188025	IEA					P	HPO:iea[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0002021	OMIM:188025	IEA					P	HPO:iea[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0000508	OMIM:188025	IEA					P	HPO:iea[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0003010	OMIM:188025	IEA					P	HPO:iea[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0009466	OMIM:188025	IEA					P	HPO:iea[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0030084	OMIM:188025	TAS					P	HPO:skoehler[2014-09-21]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0003745	OMIM:188025	IEA					I	HPO:iea[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0001873	OMIM:188025	IEA					P	HPO:iea[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0000347	OMIM:188025	TAS					P	HPO:skoehler[2009-02-17]
OMIM:188025	Thrombocytopenia, Paris-Trousseau type		HP:0001249	OMIM:188025	IEA					P	HPO:iea[2009-02-17]
OMIM:604250	Hemochromatosis, type 3		HP:0000044	PMID:12130528	PCS					P	HPO:probinson[2013-02-19]
OMIM:604250	Hemochromatosis, type 3		HP:0003452	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0000141	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0001394	PMID:10802645	PCS		2/7			P	HPO:probinson[2013-02-19];HPO:probinson[2021-10-04]
OMIM:604250	Hemochromatosis, type 3		HP:0003281	PMID:10802645	PCS		7/7			P	HPO:probinson[2013-02-19];HPO:probinson[2021-10-04]
OMIM:604250	Hemochromatosis, type 3		HP:0012378	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0012463	PMID:10802645	PCS		7/7			P	HPO:probinson[2021-10-04]
OMIM:604250	Hemochromatosis, type 3		HP:0001903	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0000979	OMIM:604250	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604250	Hemochromatosis, type 3		HP:0000007	PMID:11313241	PCS					I	HPO:probinson[2013-01-09]
OMIM:604250	Hemochromatosis, type 3		HP:0000953	PMID:10802645	PCS		4/7			P	HPO:probinson[2013-02-19];HPO:probinson[2021-10-04]
OMIM:604250	Hemochromatosis, type 3		HP:0001888	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0001638	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0000802	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0002910	PMID:10802645	PCS		5/7			P	HPO:probinson[2013-02-19];HPO:probinson[2021-10-04]
OMIM:604250	Hemochromatosis, type 3		HP:0001369	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604250	Hemochromatosis, type 3		HP:0001875	OMIM:604250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001298	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000486	OMIM:220111	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001332	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001250	OMIM:220111	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001252	PMID:26510951	PCS		5/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001251	OMIM:220111	IEA					P	HPO:iea[2009-02-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0003593	PMID:26510951	PCS		1/10			C	HPO:probinson[2012-04-11];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0003074	OMIM:220111	TAS					P	HPO:skoehler[2013-01-22]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0010883	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000639	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0011220	PMID:26510951	PCS		1/10			P	HPO:skoehler[2012-10-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001647	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000316	OMIM:220111	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0020045	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001522	PMID:26510951	PCS		3/10			C	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001007	PMID:26510951	PCS		2/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0003623	PMID:26510951	PCS		6/10			C	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002553	OMIM:220111	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000252	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002078	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0011968	PMID:26510951	PCS		7/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002197	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001263	OMIM:220111	TAS		10/10			P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002151	PMID:26510951	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000294	OMIM:220111	IEA					P	HPO:iea[2009-02-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0011800	OMIM:220111	TAS					P	HPO:skoehler[2013-11-28]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0033379	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0011096	OMIM:220111	TAS					P	HPO:skoehler[2013-01-22]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000007	PMID:12529507	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001338	PMID:26510951	PCS		1/6			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000565	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000047	PMID:26510951	PCS		2/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001653	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001257	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002789	OMIM:220111	TAS					P	HPO:skoehler[2013-01-22]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000369	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001414	OMIM:220111	TAS					P	HPO:skoehler[2013-01-22]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001337	OMIM:220111	IEA					P	HPO:iea[2009-02-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0003577	PMID:26510951	PCS		3/10			C	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000463	OMIM:220111	IEA					P	HPO:iea[2009-02-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001310	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000023	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002919	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001508	PMID:26510951	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0011560	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001987	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001943	PMID:26510951	PCS		3/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001946	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0025116	PMID:26510951	PCS		3/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0007305	OMIM:220111	TAS					P	HPO:probinson[2012-04-11]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001545	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0003128	OMIM:220111	TAS		10/10			P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0004898	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0003645	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001320	PMID:26510951	PCS		1/6			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002015	PMID:26510951	PCS		2/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000750	PMID:26510951	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000431	PMID:26510951	PCS		2/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000474	PMID:26510951	PCS		2/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002013	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001680	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000272	OMIM:220111	TAS					P	HPO:probinson[2012-04-11]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002171	OMIM:220111	TAS					P	HPO:probinson[2009-02-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0002490	PMID:26510951	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0100598	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001639	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0033044	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001518	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000822	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0001712	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0008347	PMID:26510951	PCS		10/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0006565	OMIM:220111	IEA					P	HPO:iea[2009-02-17]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0004900	PMID:26510951	PCS		1/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0000347	PMID:26510951	PCS		2/10			P	HPO:probinson[2023-02-19]
OMIM:220111	Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)		HP:0009879	PMID:26510951	PCS		1/6			P	HPO:probinson[2023-02-19]
OMIM:616654	Joubert syndrome 24		HP:0003577	PMID:25118024	PCS		1/1			C	HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001344	OMIM:616654	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616654	Joubert syndrome 24		HP:0001762	OMIM:616654	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616654	Joubert syndrome 24		HP:0001321	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001310	OMIM:616654	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616654	Joubert syndrome 24		HP:0001288	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0000540	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001162	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001263	PMID:25118024	PCS		1/1		HP:0012828	P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001252	PMID:25118024	PCS	HP:0003577	1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001251	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0003593	OMIM:616654	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616654	Joubert syndrome 24		HP:0000639	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0000007	PMID:21565611	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001302	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001830	PMID:25118024	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001257	PMID:25118024	PCS	HP:0003621	1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0002126	PMID:25118024	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:616654	Joubert syndrome 24		HP:0001347	PMID:25118024	PCS	HP:0003621	1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-17]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000486	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001250	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001252	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0004383	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001508	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0002719	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0010055	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-06-08]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0008872	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001748	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0009765	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0002219	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000218	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001522	PMID:16783566;PMID:17855048	PCS					C	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001466	PMID:16783566	PCS					I	HPO:probinson[2022-09-04]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001249	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000077	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000494	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000252	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0010815	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0002650	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001442	PMID:16783566;PMID:17855048	PCS					I	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001263	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0011304	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0009553	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001999	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000448	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000329	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0004209	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000444	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000545	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0001513	PMID:17855048	PCS					P	HPO:iea[2012-04-24]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000347	PMID:16783566;PMID:17855048	PCS					P	HPO:iea[2012-06-08]
OMIM:610543	Chromosome 16p13.3 deletion syndrome		HP:0000006	PMID:16783566	PCS					I	HPO:probinson[2022-09-04]
OMIM:619201	Nephrotic syndrome, type 23		HP:0003621	PMID:31472902	PCS		1/2			C	HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0012574	PMID:31472902	PCS		1/2			P	HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0011463	PMID:31472902	PCS		1/2			C	HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0000097	PMID:31472902	PCS		1/2			P	HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0000007	PMID:31472902	PCS					I	HPO:probinson[2021-05-11];HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0031266	PMID:31472902	PCS		1/2			P	HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0000093	PMID:31472902	PCS		2/2			P	HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0012588	PMID:31472902	PCS		2/2			P	HPO:probinson[2021-05-11]
OMIM:619201	Nephrotic syndrome, type 23		HP:0012579	PMID:31472902	PCS		1/2			P	HPO:probinson[2021-05-11]
OMIM:612354	Inflammatory bowel disease 21		HP:0100279	OMIM:612354	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612354	Inflammatory bowel disease 21		HP:0000006	OMIM:612354	TAS					I	HPO:skoehler[2017-07-13]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0002223	PMID:9326952	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0000561	PMID:9326952	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0003577	PMID:9326952	PCS		1/1			C	HPO:probinson[2022-04-24]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0000970	PMID:10233227	PCS		1/1			P	HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0001030	PMID:10233227	PCS		1/1			P	HPO:skoehler[2015-01-14];HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0002293	PMID:9326952	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0008070	PMID:10233227	PCS		1/1			P	HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0008391	PMID:10233227	PCS		1/1			P	HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0000968	PMID:10233227	PCS					P	HPO:skoehler[2015-01-14];HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0008066	PMID:10233227	PCS		1/1			P	HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0040189	PMID:10233227	PCS		1/1			P	HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0000007	PMID:10233227	PCS					I	HPO:probinson[2020-05-10]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0000972	PMID:9326952;PMID:10233227	PCS		2/2			P	HPO:probinson[2020-05-10];HPO:probinson[2022-04-24]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0007446	PMID:9326952	PCS	HP:0003577	1/1			P	HPO:probinson[2022-04-24]
OMIM:604536	Ectodermal dysplasia/skin fragility syndrome		HP:0008404	PMID:9326952	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:607017	Deafness, autosomal dominant 21		HP:0003577	PMID:32631815	PCS		1/41			C	HPO:probinson[2022-04-16];HPO:probinson[2022-04-16]
OMIM:607017	Deafness, autosomal dominant 21		HP:0003621	PMID:32631815	PCS		8/41			C	HPO:probinson[2022-04-16];HPO:probinson[2022-04-16]
OMIM:607017	Deafness, autosomal dominant 21		HP:0003596	PMID:32631815	PCS		10/41			C	HPO:probinson[2022-04-16];HPO:probinson[2022-04-16]
OMIM:607017	Deafness, autosomal dominant 21		HP:0000407	PMID:32631815	PCS					P	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-16]
OMIM:607017	Deafness, autosomal dominant 21		HP:0011463	PMID:32631815	PCS		2/41			C	HPO:probinson[2022-04-16];HPO:probinson[2022-04-16]
OMIM:607017	Deafness, autosomal dominant 21		HP:0011462	PMID:32631815	PCS		19/41			C	HPO:probinson[2022-04-16];HPO:probinson[2022-04-16]
OMIM:607017	Deafness, autosomal dominant 21		HP:0000006	PMID:32631815	PCS					I	HPO:skoehler[2015-09-11];HPO:probinson[2022-04-16]
OMIM:607017	Deafness, autosomal dominant 21		HP:0003623	PMID:32631815	PCS		1/41			C	HPO:probinson[2022-04-16];HPO:probinson[2022-04-16]
OMIM:601466	Patent ductus venosus		HP:0001397	OMIM:601466	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601466	Patent ductus venosus		HP:0012022	OMIM:601466	TAS					P	HPO:probinson[2012-07-26]
OMIM:601466	Patent ductus venosus		HP:0001410	OMIM:601466	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601466	Patent ductus venosus		HP:0012024	OMIM:601466	TAS					P	HPO:skoehler[2012-07-27]
OMIM:601466	Patent ductus venosus		HP:0001419	OMIM:601466	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:601466	Patent ductus venosus		HP:0012021	OMIM:601466	TAS					P	HPO:probinson[2012-07-26]
OMIM:601466	Patent ductus venosus		HP:0001987	OMIM:601466	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601466	Patent ductus venosus		HP:0002480	OMIM:601466	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601466	Patent ductus venosus		HP:0000007	OMIM:601466	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0004325	PMID:33513338	PCS		6/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000684	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002540	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001773	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002783	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001250	PMID:33513338	PCS		6/10			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001252	PMID:33513338	PCS		17/35			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001251	PMID:33513338	PCS		2/11			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002020	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002061	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0010841	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0011412	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0011410	PMID:33513338	PCS		6/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000958	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000319	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000717	PMID:33513338	PCS		5/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000713	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0025336	PMID:33513338	PCS		6/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002019	PMID:33513338	PCS		6/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001249	PMID:33513338	PCS					P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000358	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000494	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000252	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000010	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001344	PMID:33513338	PCS		11/11			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002353	PMID:33513338	PCS		8/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000574	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001382	PMID:33513338	PCS		4/16			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001260	PMID:33513338	PCS		5/8			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001263	PMID:33513338	PCS		21/22			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0004691	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0011800	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0011169	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0031355	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0031951	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002307	PMID:33513338	PCS		7/16			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001852	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0007359	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001257	PMID:33513338	PCS		3/16			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000006	PMID:33513338	PCS					I	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000248	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001337	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0006986	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001336	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000687	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002521	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000540	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002121	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001197	PMID:33513338	PCS		2/15			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002283	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001270	PMID:33513338	PCS		21/23			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001629	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0011166	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0006297	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000733	PMID:33513338	PCS		7/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000736	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002119	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0012171	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001622	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0006834	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0008936	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001562	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000670	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0006956	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002015	PMID:33513338	PCS		5/15			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000750	PMID:33513338	PCS		21/23			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002650	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002133	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0031936	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0002376	PMID:33513338	PCS		4/21			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0010818	PMID:33513338	PCS		6/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0005484	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0011421	PMID:33513338	PCS		4/25			C	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000705	PMID:33513338	PCS		4/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0006482	PMID:33513338	PCS					P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0011197	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0006286	PMID:33513338	PCS		5/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000349	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000348	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0025502	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0000504	PMID:33513338	PCS		3/12			P	HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001511	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0200055	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0004789	PMID:33513338	PCS		2/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:619229	Kohlschutter-Tonz syndrome-like		HP:0001513	PMID:33513338	PCS		3/25			P	HPO:probinson[2021-06-20];HPO:probinson[2021-06-20]
OMIM:615413	Spermatogenic failure 12		HP:0000789	PMID:23315541	PCS					P	HPO:skoehler[2013-09-30]
OMIM:615413	Spermatogenic failure 12		HP:0012863	PMID:23315541	PCS					P	HPO:lccarmody[2018-06-13]
OMIM:615413	Spermatogenic failure 12		HP:0000006	PMID:23315541	PCS					I	HPO:skoehler[2013-09-30]
OMIM:615413	Spermatogenic failure 12		HP:0000027	PMID:23315541	PCS					P	HPO:skoehler[2013-09-30]
OMIM:154600	Marcus gunn phenomenon		HP:0007970	OMIM:154600	TAS				HP:0012833	P	HPO:skoehler[2010-06-20]
OMIM:154600	Marcus gunn phenomenon		HP:0007687	OMIM:154600	TAS					P	HPO:probinson[2009-02-17]
OMIM:154600	Marcus gunn phenomenon		HP:0000006	OMIM:154600	TAS					I	HPO:probinson[2009-02-17]
OMIM:613704	Microphthalmia, isolated 7		HP:0003577	PMID:19864492	PCS					C	HPO:probinson[2021-10-10]
OMIM:613704	Microphthalmia, isolated 7		HP:0000568	PMID:19864492	PCS		2/3			P	HPO:probinson[2013-01-09];HPO:probinson[2021-10-10]
OMIM:613704	Microphthalmia, isolated 7		HP:0000006	PMID:19864492	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-10]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0005546	OMIM:604278	IEA					P	HPO:iea[2009-02-17]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0410288	PMID:10545938	PCS		2/2			P	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0000585	PMID:8142230;PMID:10545938	PCS		3/3			P	HPO:probinson[2022-03-07];HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0004322	PMID:8142230;PMID:10545938	PCS		3/3			P	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0025708	PMID:10545938	PCS		1/2			C	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0000518	PMID:8142230;PMID:10545938	PCS		3/3			P	HPO:probinson[2022-03-07];HPO:skoehler[2010-06-18];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0011463	PMID:10545938	PCS		1/2			C	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0032066	PMID:8142230	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:4000010	PMID:8142230	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0000007	PMID:10545938	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0002900	PMID:8142230	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0001995	OMIM:604278	IEA					P	HPO:iea[2009-02-17]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0001510	PMID:10545938	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0002514	PMID:8142230	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0002049	PMID:8142230;PMID:10545938	PCS		3/3			P	HPO:probinson[2022-03-07];HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0001249	PMID:8142230;PMID:10545938	PCS		3/3			P	HPO:probinson[2022-03-07];HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0000501	PMID:8142230;PMID:10545938	PCS		3/3			P	HPO:probinson[2022-03-07];HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0004910	PMID:10545938	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:604278	Renal tubular acidosis, proximal, with ocular abnormalities and mentalretardation		HP:0001942	PMID:8142230	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:618889	Liberfarb syndrome		HP:0002663	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0007737	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0007814	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0000252	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0002650	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0004322	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0001263	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0031367	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0000407	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0000007	PMID:31263216	PCS					I	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0000546	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0000543	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:618889	Liberfarb syndrome		HP:0001249	PMID:31263216	PCS					P	HPO:probinson[2020-07-24]
OMIM:150300	Larynx, congenital partial atresia of		HP:0005950	OMIM:150300	IEA					P	HPO:iea[2009-02-17]
OMIM:150300	Larynx, congenital partial atresia of		HP:0005945	OMIM:150300	IEA					P	HPO:iea[2009-02-17]
OMIM:150300	Larynx, congenital partial atresia of		HP:0000006	OMIM:150300	IEA					I	HPO:iea[2009-02-17]
OMIM:617562	Meckel syndrome 13		HP:0001321	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0001371	OMIM:617562	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617562	Meckel syndrome 13		HP:0001263	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0002085	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0001251	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0000657	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0002419	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0000007	OMIM:617562	IEA					I	HPO:skoehler[2019-04-18]
OMIM:617562	Meckel syndrome 13		HP:0000488	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0000113	OMIM:617562	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617562	Meckel syndrome 13		HP:0001249	OMIM:617562	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617562	Meckel syndrome 13		HP:0000347	OMIM:617562	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001276	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000365	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002540	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000023	PMID:30464055	PCS		1/2			P	HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001371	PMID:30464055	PCS	HP:0003593	2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001274	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002020	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001508	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0012471	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0011682	PMID:30464055	PCS		1/2			P	HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000519	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0007024	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002119	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000218	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002835	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000776	PMID:30464055	PCS	HP:0003577	1/2			P	HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001347	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002510	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001762	PMID:30464055	PCS		1/2			P	HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0030048	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002197	PMID:30464055	PCS	HP:0003623	2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0003819	PMID:30464055	IEA		2/2			C	HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002827	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001537	PMID:30464055	PCS		1/2			P	HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000007	PMID:30464055	PCS					I	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0002507	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000648	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000527	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0001511	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0007359	PMID:30464055	PCS	HP:0003623	2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000325	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618651	Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies		HP:0000347	PMID:30464055	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0003477	PMID:26556829	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0011463	PMID:26556829	PCS					C	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0011462	PMID:26556829	PCS					C	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0009027	PMID:26556829	PCS		11/29			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0002936	PMID:26556829	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0001249	PMID:26556829	PCS		3/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0008956	PMID:26556829	PCS		1/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0002751	PMID:26556829	PCS		17/29			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0003621	PMID:26556829	PCS					C	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0003487	PMID:26556829	PCS		2/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0008959	PMID:26556829	PCS		16/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0001288	PMID:26556829	PCS		18/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0002079	PMID:26556829	PCS		3/29			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0001761	PMID:26556829	PCS		23/29			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0002174	PMID:26556829	PCS		10/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0009053	PMID:26556829	PCS		29/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0008981	PMID:26556829	PCS		4/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0000007	PMID:26556829	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0001239	PMID:26556829	PCS		3/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0006466	PMID:26556829	PCS		14/29			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0002403	PMID:26556829	PCS		7/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0001257	PMID:26556829	PCS		0/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0002522	PMID:26556829	PCS		8/29			P	HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0003677	PMID:26556829	PCS					C	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04];HPO:probinson[2023-03-13]
OMIM:616668	Charcot-Marie-Tooth disease, axonal, type 2X		HP:0008944	PMID:26556829	PCS		20/29			P	HPO:probinson[2023-03-13]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0005942	PMID:8585561	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-14]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0005576	OMIM:263000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0002098	OMIM:263000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0003593	OMIM:263000	TAS					C	HPO:skoehler[2015-12-30]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0033246	PMID:2166657	PCS					P	HPO:probinson[2021-02-13]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0012735	OMIM:263000	TAS					P	HPO:skoehler[2014-03-24]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0001508	OMIM:263000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0001939	OMIM:263000	IEA					P	HPO:iea[2009-02-17]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0000007	PMID:8585561	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-14]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0002878	OMIM:263000	TAS	HP:0003593				P	HPO:probinson[2014-05-29]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0001648	OMIM:263000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0000961	OMIM:263000	IEA					P	HPO:iea[2009-02-17]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0002788	OMIM:263000	IEA					P	HPO:iea[2009-02-17]
OMIM:263000	Interstitial pneumonitis, desquamative, familial		HP:0002789	OMIM:263000	IEA					P	HPO:iea[2009-02-17]
OMIM:611107	Intellectual developmental disorder, autosomal recessive 4		HP:0000582	OMIM:611107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611107	Intellectual developmental disorder, autosomal recessive 4		HP:0000252	OMIM:611107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611107	Intellectual developmental disorder, autosomal recessive 4		HP:0001263	OMIM:611107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611107	Intellectual developmental disorder, autosomal recessive 4		HP:0000272	OMIM:611107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611107	Intellectual developmental disorder, autosomal recessive 4		HP:0012448	OMIM:611107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611107	Intellectual developmental disorder, autosomal recessive 4		HP:0000007	OMIM:611107	TAS					I	HPO:skoehler[2017-07-13]
OMIM:611107	Intellectual developmental disorder, autosomal recessive 4		HP:0001249	OMIM:611107	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0002014	OMIM:607765	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0002630	OMIM:607765	TAS					P	HPO:probinson[2014-05-24]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0001399	OMIM:607765	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0003256	OMIM:607765	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0003146	OMIM:607765	TAS					P	HPO:probinson[2014-05-24]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0001394	OMIM:607765	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0002240	PMID:12679481	PCS		12/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0002570	PMID:12679481	PCS		6/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:6000825	PMID:11067870	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0011985	PMID:12679481	PCS		2/13			P	HPO:skoehler[2013-06-05];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0200084	PMID:12679481	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0002908	PMID:12679481	PCS					P	HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0001508	OMIM:607765	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0002748	PMID:12679481	PCS		5/13			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0000007	PMID:11067870	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0001406	PMID:12679481	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0002910	PMID:12679481	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0000952	PMID:12679481	PCS		7/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0001744	OMIM:607765	TAS		3/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:607765	Bile acid synthesis defect, congenital, 1		HP:0003623	PMID:12679481	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-20]
OMIM:608456	Familial adenomatous polyposis, 2		HP:0005227	OMIM:608456	TAS					P	HPO:probinson[2013-03-25]
OMIM:608456	Familial adenomatous polyposis, 2		HP:0003003	PMID:12606733	TAS		5/12			P	HPO:probinson[2013-03-25]
OMIM:608456	Familial adenomatous polyposis, 2		HP:0000007	OMIM:608456	TAS					I	HPO:probinson[2013-01-09]
OMIM:617576	Spermatogenic failure 18		HP:0033393	PMID:24360805	PCS		7/7			P	HPO:probinson[2023-02-24]
OMIM:617576	Spermatogenic failure 18		HP:0032560	PMID:24360805	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-24]
OMIM:617576	Spermatogenic failure 18		HP:0003251	PMID:24360805	PCS		7/7			P	HPO:probinson[2023-02-24]
OMIM:617576	Spermatogenic failure 18		HP:0011462	PMID:24360805	PCS		7/7			C	HPO:probinson[2023-02-24]
OMIM:617576	Spermatogenic failure 18		HP:0000007	PMID:24360805	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-24]
OMIM:617576	Spermatogenic failure 18		HP:0012207	PMID:24360805	PCS		7/7			P	HPO:probinson[2023-02-24]
OMIM:617576	Spermatogenic failure 18		HP:0032558	PMID:24360805	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-24]
OMIM:617576	Spermatogenic failure 18		HP:0032559	PMID:24360805	PCS		7/7			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-24]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0001265	OMIM:613710	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0001254	OMIM:613710	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0003477	OMIM:613710	TAS	HP:0011463				P	HPO:skoehler[2012-10-17]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0003202	PMID:19798730	PCS		2/4			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0003621	PMID:19798730	PCS		2/4			C	HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0001762	OMIM:613710	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0001288	PMID:19798730	PCS		4/4			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0005750	PMID:19798730	PCS		2/4			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0002460	PMID:19798730	PCS		4/4			P	HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0002490	PMID:19798730	PCS		3/3			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0003470	OMIM:613710	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0011463	PMID:19798730	PCS		2/4			C	HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0000007	PMID:19798730	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0002936	PMID:19798730	PCS		1/4			P	HPO:probinson[2022-08-26]
OMIM:613710	Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degenerationand progressive polyneuropathy type)		HP:0001324	OMIM:613710	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0002135	OMIM:615361	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0003401	PMID:23802516	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-03]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0003394	PMID:23802516	PCS		1/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-03]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0003581	PMID:23802516	PCS		2/2			C	HPO:probinson[2023-04-03]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0008897	OMIM:615361	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0100529	PMID:23802516	PCS		0/2			P	HPO:probinson[2023-04-03]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0002901	PMID:23802516	PCS		2/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-03]
OMIM:615361	Hypocalcemia, autosomal dominant 2		HP:0000006	PMID:23802516	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-04-03]
OMIM:267500	Reticular dysgenesia		HP:0001882	PMID:19043417	PCS					P	HPO:probinson[2017-12-22]
OMIM:267500	Reticular dysgenesia		HP:0005387	PMID:19043417	PCS					P	HPO:probinson[2017-12-22]
OMIM:267500	Reticular dysgenesia		HP:0005541	PMID:19043417	PCS					P	HPO:probinson[2017-12-22]
OMIM:267500	Reticular dysgenesia		HP:0005354	OMIM:267500	TAS					P	HPO:probinson[2017-12-22]
OMIM:267500	Reticular dysgenesia		HP:0000778	PMID:19043417	PCS					P	HPO:probinson[2017-12-22]
OMIM:267500	Reticular dysgenesia		HP:0100806	PMID:19043417	PCS					P	HPO:probinson[2017-12-22]
OMIM:267500	Reticular dysgenesia		HP:0000007	OMIM:267500	IEA					I	HPO:iea[2009-02-17]
OMIM:267500	Reticular dysgenesia		HP:0001888	PMID:19043417	PCS					P	HPO:probinson[2017-12-22]
OMIM:267500	Reticular dysgenesia		HP:0011840	OMIM:267500	TAS					P	HPO:probinson[2017-12-22]
OMIM:613076	Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay		HP:0000518	PMID:19409522	PCS					P	HPO:probinson[2013-04-14]
OMIM:613076	Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay		HP:0003198	PMID:19409522	PCS					P	HPO:probinson[2013-04-14]
OMIM:613076	Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay		HP:0000407	PMID:19409522	PCS					P	HPO:probinson[2013-01-09]
OMIM:613076	Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay		HP:0001263	PMID:19409522	PCS					P	HPO:probinson[2013-04-14]
OMIM:613076	Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay		HP:0000519	OMIM:613076	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613076	Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay		HP:0008972	PMID:19409522	PCS					P	HPO:probinson[2013-04-14]
OMIM:613076	Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay		HP:0000007	PMID:19409522	PCS					I	HPO:probinson[2013-04-14]
OMIM:618123	Polydactyly, postaxial, type A8		HP:0100259	PMID:28973407	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-06-20]
OMIM:618123	Polydactyly, postaxial, type A8		HP:0003577	PMID:28973407	PCS		10/10			C	HPO:probinson[2021-06-20]
OMIM:618123	Polydactyly, postaxial, type A8		HP:0004322	PMID:28973407	PCS		3/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-20]
OMIM:618123	Polydactyly, postaxial, type A8		HP:0002164	PMID:28973407	PCS		1/10		HP:0012825	P	HPO:probinson[2021-06-20]
OMIM:618123	Polydactyly, postaxial, type A8		HP:0000007	PMID:28973407	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-20]
OMIM:618123	Polydactyly, postaxial, type A8		HP:0002857	PMID:28973407	PCS		2/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-20]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0001265	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0002650	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0001761	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003693	OMIM:601472	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003484	OMIM:601472	TAS					P	HPO:probinson[2012-03-15]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0002460	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003392	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003393	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0002172	OMIM:601472	IEA					P	HPO:skoehler[2019-02-22]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0011462	PMID:12690580	PCS					C	HPO:probinson[2022-08-12]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0002936	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003426	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003427	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0009129	OMIM:601472	TAS					P	HPO:probinson[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0000006	PMID:12690580	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-12]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003435	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0003677	OMIM:601472	IEA					C	HPO:iea[2009-02-17]
OMIM:601472	Charcot-Marie-Tooth disease, axonal, type 2D		HP:0001765	OMIM:601472	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0002025	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0007759	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000365	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000431	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000023	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000232	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000482	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000691	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000506	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000618	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000316	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000327	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000668	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0001537	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000238	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0030680	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0001627	OMIM:601499	TAS					P	HPO:skoehler[2015-12-30]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000047	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000322	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000006	OMIM:601499	IEA					I	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000028	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000303	OMIM:601499	IEA					P	HPO:skoehler[2010-06-20]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0000501	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:601499	Axenfeld-rieger syndrome, type 2		HP:0007833	OMIM:601499	IEA					P	HPO:iea[2009-02-17]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000175	PMID:34750192	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0003577	PMID:34750192	PCS		10/10			C	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000365	PMID:34750192	PCS		6/6			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000293	PMID:34750192	PCS		8/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000160	PMID:34750192	PCS		8/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0001263	PMID:34750192	PCS		0/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0004451	PMID:34750192	PCS		2/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000162	PMID:34750192	PCS		4/9			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0030022	PMID:34750192	PCS		8/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000006	PMID:34750192	PCS					I	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0002104	PMID:34750192	PCS		4/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000347	PMID:34750192	PCS		6/10			P	HPO:probinson[2024-03-02]
OMIM:620457	Auriculocondylar syndrome 4		HP:0000324	PMID:34750192	PCS		6/10			P	HPO:probinson[2024-03-02]
OMIM:605827	Basaloid follicular hamartoma syndrome, generalized, autosomal dominant		HP:0002209	OMIM:605827	IEA					P	HPO:iea[2009-02-17]
OMIM:605827	Basaloid follicular hamartoma syndrome, generalized, autosomal dominant		HP:0010566	OMIM:605827	IEA					P	HPO:skoehler[2010-06-20]
OMIM:605827	Basaloid follicular hamartoma syndrome, generalized, autosomal dominant		HP:0010610	OMIM:605827	IEA					P	HPO:skoehler[2010-06-18]
OMIM:605827	Basaloid follicular hamartoma syndrome, generalized, autosomal dominant		HP:0025249	OMIM:605827	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605827	Basaloid follicular hamartoma syndrome, generalized, autosomal dominant		HP:0000966	OMIM:605827	IEA					P	HPO:iea[2009-02-17]
OMIM:605827	Basaloid follicular hamartoma syndrome, generalized, autosomal dominant		HP:0200034	OMIM:605827	IEA					P	HPO:skoehler[2010-06-20]
OMIM:605827	Basaloid follicular hamartoma syndrome, generalized, autosomal dominant		HP:0000006	OMIM:605827	IEA					I	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0002069	PMID:33407268	PCS		2/5			P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0002267	PMID:33407268	PCS		5/5			P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0001278	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0004343	OMIM:268800	IEA					P	HPO:skoehler[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0010829	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0000020	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0001252	PMID:33407268	PCS		2/5			P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0001251	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0010729	PMID:33407268	PCS		5/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0003593	PMID:33407268	PCS		5/5			C	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0002240	PMID:33407268	PCS		1/5		HP:0012825	P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0002380	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0032794	PMID:33407268	PCS		3/5			P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0000280	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0000618	PMID:23785136	PCS	HP:0003593				P	HPO:probinson[2014-03-23]
OMIM:268800	Sandhoff disease		HP:0000975	OMIM:268800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268800	Sandhoff disease		HP:0003429	PMID:33407268	PCS		1/5			P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0000158	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0001324	OMIM:268800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:268800	Sandhoff disease		HP:0000256	PMID:33407268	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0001347	PMID:33407268	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0003202	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0001640	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0002574	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0002376	PMID:33407268	PCS		5/5			P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0001260	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:6000122	OMIM:268800	TAS					P	HPO:probinson[2024-01-06]
OMIM:268800	Sandhoff disease		HP:0002493	OMIM:268800	TAS					P	HPO:skoehler[2018-10-08]
OMIM:268800	Sandhoff disease		HP:0033978	PMID:33407268	PCS		5/5			P	HPO:probinson[2021-07-16]
OMIM:268800	Sandhoff disease		HP:0007272	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0003819	PMID:33407268	PCS		5/5			C	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0000007	PMID:33407268	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0000802	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0000966	OMIM:268800	IEA					P	HPO:skoehler[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0001433	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:268800	Sandhoff disease		HP:0001257	PMID:33407268	PCS		2/5			P	HPO:probinson[2021-06-23]
OMIM:268800	Sandhoff disease		HP:0002028	OMIM:268800	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0002983	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0002089	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0001234	PMID:8571951;PMID:15316973	PCS		11/11			P	HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0005257	PMID:8571951	PCS	HP:0003577				P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0032930	PMID:8571951	PCS	HP:0003577				P	HPO:probinson[2020-03-31]
OMIM:256050	Atelosteogenesis, type II		HP:0002938	PMID:8571951	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0006375	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0003826	PMID:8571951	PCS		2/3			C	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0001522	PMID:15316973	PCS		1/1			C	HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0003864	PMID:8571951	PCS	HP:0003577				P	HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0000175	PMID:8571951	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0009826	PMID:8571951	PCS	HP:0003577				P	HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0002650	PMID:8571951	PCS	HP:0003577				P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0001762	PMID:8571951	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0003440	PMID:8571951	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0003185	OMIM:256050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256050	Atelosteogenesis, type II		HP:0030320	PMID:15316973	PCS		1/1			P	HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0000272	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0000470	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0011800	OMIM:256050	TAS					P	HPO:skoehler[2013-11-28]
OMIM:256050	Atelosteogenesis, type II		HP:0002093	PMID:8571951	PCS	HP:0003623				P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0005280	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0003180	PMID:8571951	PCS					P	HPO:iea[2012-09-10];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0000926	PMID:8571951	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0005819	OMIM:256050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0000007	PMID:8571951	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0002947	PMID:8571951	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0003417	PMID:8571951	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2019-12-14]
OMIM:256050	Atelosteogenesis, type II		HP:0001852	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0000347	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:256050	Atelosteogenesis, type II		HP:0002644	OMIM:256050	IEA					P	HPO:iea[2009-02-17]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001058	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000023	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002286	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0005353	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001350	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0003593	PMID:36112693	PCS		4/4			C	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001072	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002719	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000958	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001508	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001903	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0012393	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002937	PMID:36112693	PCS		2/2			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0007441	PMID:36112693	PCS		3/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001328	PMID:36112693	PCS		3/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002837	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000337	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0003508	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002216	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000494	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000750	PMID:36112693	PCS		3/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000970	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001047	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002373	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0011968	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002099	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000729	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000007	PMID:36112693	PCS					I	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000964	PMID:36112693	PCS	HP:0003593	2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001954	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000403	PMID:36112693	PCS		3/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000967	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001511	PMID:36112693	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000047	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0001876	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0000028	PMID:36112693	PCS		1/4			P	HPO:probinson[2023-06-18]
OMIM:620331	Hatipoglu immunodeficiency syndrome		HP:0002721	PMID:36112693	PCS		4/4			P	HPO:probinson[2023-06-18]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0002465	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0000365	OMIM:616683	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0001272	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0001371	PMID:27120463;PMID:26307567	PCS		20/20			P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0002384	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0001252	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0006808	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0012448	OMIM:616683	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0007281	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0012332	OMIM:616683	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0100704	OMIM:616683	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0007663	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0002119	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0005968	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0002019	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0001249	OMIM:616683	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0008936	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0000011	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0000252	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0001344	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0002079	PMID:27120463;PMID:26307567	PCS		20/20			P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0001263	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0005484	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0011344	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0000007	OMIM:616683	PCS					I	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0000648	PMID:27120463	PCS					P	HPO:probinson[2017-06-17]
OMIM:616683	Leukodystrophy, hypomyelinating, 12		HP:0001257	PMID:26307567	PCS					P	HPO:probinson[2017-06-17]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001320	PMID:32169168	PCS		1/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0025352	PMID:32169168	PCS					I	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0000750	PMID:32169168	PCS		4/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0002376	PMID:32169168	PCS	HP:0011463				P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0031936	PMID:32169168	PCS	HP:0003593	3/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001250	PMID:32169168	IEA		4/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001272	PMID:32169168	PCS		1/4		HP:0012825	P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001263	PMID:32169168	PCS		4/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0002063	PMID:32169168	PCS		2/2			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001251	PMID:32169168	PCS		4/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0002080	PMID:32169168	PCS		4/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0002725	PMID:32169168	PCS		1/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001312	PMID:32169168	PCS		1/4			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0000006	PMID:32169168	PCS					I	HPO:probinson[2022-09-04]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001336	PMID:32169168	PCS		3/3			P	HPO:probinson[2020-07-24]
OMIM:618876	Epilepsy, progressive myoclonic, 11		HP:0001347	PMID:32169168	PCS		2/3			P	HPO:probinson[2020-07-24]
OMIM:616697	Deafness, autosomal dominant 69		HP:0000407	PMID:26522471	PCS					P	HPO:probinson[2017-06-17]
OMIM:616697	Deafness, autosomal dominant 69		HP:0000006	PMID:26522471	PCS					I	HPO:probinson[2017-06-17]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000582	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0002188	PMID:32220291	PCS		2/4			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0004322	PMID:32220291	PCS		2/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001250	PMID:32220291	PCS		4/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001290	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001270	PMID:32220291	PCS		4/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0012741	PMID:32220291	PCS		1/4	MALE		P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0011182	PMID:32220291	PCS		3/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0100704	PMID:32220291	PCS		3/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000219	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000218	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000311	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001249	PMID:32220291	PCS		4/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001601	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000577	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0008936	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0003202	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001561	PMID:32220291	PCS	HP:0011461	1/4			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000252	PMID:32220291	PCS	HP:0011461	1/4			P	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000252	PMID:32220291	PCS		4/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001344	PMID:32220291	PCS		3/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0031936	PMID:32220291	PCS		2/2			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0002079	PMID:32220291	PCS		2/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0005487	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0011968	PMID:32220291	PCS		4/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001263	PMID:32220291	PCS		4/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0009890	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0010880	PMID:32220291	PCS	HP:0011461	1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0007112	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000007	PMID:32220291	PCS					I	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001357	PMID:32220291	PCS		2/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0001257	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000300	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:618862	Neurodevelopmental disorder with hypotonia, microcephaly, and seizures		HP:0000248	PMID:32220291	PCS		1/4			P	HPO:probinson[2020-09-03]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002025	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000286	OMIM:614080	TAS					P	HPO:skoehler[2014-03-24]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002023	PMID:21493957	TAS					P	HPO:skoehler[2012-10-17];HPO:nvasilevsky[2019-04-01]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002265	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001250	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001252	OMIM:614080	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0003196	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002020	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001290	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000280	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000639	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0003828	OMIM:614080	TAS					M	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000316	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001643	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001249	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000358	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001265	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000175	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001344	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001266	OMIM:614080	TAS		HP:0040282			P	HPO:skoehler[2013-06-03]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001263	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000646	PMID:21493957	TAS					P	HPO:skoehler[2015-10-09];HPO:nvasilevsky[2019-04-01]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000007	OMIM:614080	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002867	OMIM:614080	TAS					P	HPO:nvasilevsky[2019-04-01]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001257	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000369	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001337	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000126	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000341	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0003577	OMIM:614080	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000343	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002089	OMIM:614080	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000463	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001272	OMIM:614080	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0009882	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001869	OMIM:614080	TAS					P	HPO:nvasilevsky[2019-04-01]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000218	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000378	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000256	OMIM:614080	TAS		HP:0040282			P	HPO:skoehler[2013-06-03]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000776	OMIM:614080	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001347	OMIM:614080	TAS		HP:0040282			P	HPO:skoehler[2013-06-03]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000396	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000110	OMIM:614080	TAS					P	HPO:nvasilevsky[2019-04-01]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002059	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001561	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000076	OMIM:614080	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000233	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001520	PMID:21493957	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000034	OMIM:614080	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000194	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000073	OMIM:614080	TAS					P	HPO:nvasilevsky[2019-04-01]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0032464	OMIM:614080	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0032465	OMIM:614080	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0005280	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0002007	OMIM:614080	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0001631	OMIM:614080	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614080	Multiple congenital anomalies-hypotonia-seizures syndrome 1		HP:0000347	OMIM:614080	TAS					P	HPO:skoehler[2014-03-24]
OMIM:613089	Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth		HP:0001442	PMID:29446767	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-12]
OMIM:613089	Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth		HP:0004099	OMIM:613089	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613089	Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth		HP:0002619	OMIM:613089	IEA					P	HPO:skoehler[2019-02-15]
OMIM:613089	Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth		HP:0001528	OMIM:613089	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:613089	Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth		HP:0031487	PMID:29446767	PCS		13/13			P	HPO:probinson[2022-09-12]
OMIM:613089	Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth		HP:0001004	OMIM:613089	IEA					P	HPO:skoehler[2019-02-15]
OMIM:613089	Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth		HP:0012721	OMIM:613089	IEA					P	HPO:skoehler[2019-02-15]
OMIM:312612	Retinitis pigmentosa 6		HP:0001133	OMIM:312612	IEA					P	HPO:iea[2009-02-17]
OMIM:312612	Retinitis pigmentosa 6		HP:0000662	OMIM:312612	IEA					P	HPO:iea[2009-02-17]
OMIM:312612	Retinitis pigmentosa 6		HP:0000580	OMIM:312612	IEA					P	HPO:iea[2009-02-17]
OMIM:312612	Retinitis pigmentosa 6		HP:0012263	OMIM:312612	TAS					P	HPO:skoehler[2013-04-18]
OMIM:312612	Retinitis pigmentosa 6		HP:0000007	OMIM:312612	IEA					I	HPO:iea[2009-02-17]
OMIM:312612	Retinitis pigmentosa 6		HP:0001417	OMIM:312612	TAS					I	HPO:skoehler[2017-07-13]
OMIM:312612	Retinitis pigmentosa 6		HP:0000510	OMIM:312612	IEA					P	HPO:iea[2009-02-17]
OMIM:312612	Retinitis pigmentosa 6		HP:0002205	OMIM:312612	IEA					P	HPO:iea[2009-02-17]
OMIM:312612	Retinitis pigmentosa 6		HP:0200065	OMIM:312612	TAS		20/20			P	HPO:iea[2009-02-17];HPO:skoehler[2013-05-31]
OMIM:212160	Carnitine deficiency, myopathic		HP:0003234	OMIM:212160	IEA					P	HPO:skoehler[2015-12-30]
OMIM:212160	Carnitine deficiency, myopathic		HP:0003198	OMIM:212160	TAS					P	HPO:probinson[2009-02-17]
OMIM:212160	Carnitine deficiency, myopathic		HP:0030362	OMIM:212160	TAS					P	HPO:probinson[2015-11-25]
OMIM:212160	Carnitine deficiency, myopathic		HP:0000007	OMIM:212160	TAS					I	HPO:probinson[2009-02-17]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0003621	PMID:32554502	PCS		4/11			C	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000365	PMID:32554502	PCS		12/13			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000100	PMID:32554502	PCS		6/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0001272	PMID:32554502	PCS		2/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0004387	PMID:32554502	PCS		6/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000097	PMID:32554502	PCS		1/15			P	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0003593	PMID:32554502	PCS		4/11			C	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0012595	PMID:32554502	PCS		1/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0012685	PMID:32554502	PCS		2/15			P	HPO:probinson[2024-03-01];HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000518	PMID:32554502	PCS		10/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0001508	PMID:32554502	PCS		8/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0003819	PMID:32554502	PCS		7/15			C	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0011463	PMID:32554502	PCS		3/11			C	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000327	PMID:32554502	PCS		2/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000568	PMID:32554502	PCS		1/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0005528	PMID:32554502	PCS		3/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0001423	PMID:32554502	PCS					I	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000501	PMID:32554502	PCS		1/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000347	PMID:32554502	PCS		2/15			P	HPO:probinson[2024-03-01]
OMIM:301108	Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1		HP:0000962	PMID:32554502	PCS		1/15			P	HPO:probinson[2024-03-01]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0034392	PMID:37256972	PCS		3/4			P	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0000155	PMID:37256972	PCS		4/4			P	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0012344	PMID:37256972	PCS		4/4			P	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0006739	PMID:37256972	PCS		1/4			P	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0002719	PMID:37256972	PCS		2/4			P	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0011463	PMID:37256972	PCS		4/4			C	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0001888	PMID:37256972	PCS		3/4		HP:0012825	P	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0000006	PMID:37256972	PCS					I	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0200042	PMID:37256972	PCS		4/4			P	HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0011227	PMID:37256972	PCS		3/4			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:620443	Disabling pansclerotic morphea of childhood		HP:0001875	PMID:37256972	PCS		3/4		HP:0012825	P	HPO:probinson[2024-03-02]
OMIM:300216	Coats disease		HP:0012231	PMID:10484772	PCS			MALE	HP:0012833	P	HP:probinson[2018-11-04]
OMIM:300216	Coats disease		HP:0001442	PMID:10484772	PCS					I	HP:probinson[2018-11-04]
OMIM:300216	Coats disease		HP:0007763	PMID:10484772	PCS			MALE	HP:0012833	P	HP:probinson[2018-11-04]
OMIM:300216	Coats disease		HP:0000555	PMID:29567893	PCS			MALE	HP:0012833	P	HP:probinson[2018-11-04]
OMIM:192900	Vertebral hypoplasia with lumbar kyphosis		HP:0008454	OMIM:192900	IEA					P	HPO:iea[2009-02-17]
OMIM:192900	Vertebral hypoplasia with lumbar kyphosis		HP:0000006	OMIM:192900	IEA					I	HPO:iea[2009-02-17]
OMIM:192900	Vertebral hypoplasia with lumbar kyphosis		HP:0008417	OMIM:192900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0003621	PMID:23040497	PCS		4/7			C	HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0001663	PMID:23040497	PCS		1/13			P	HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0001695	PMID:23040497	PCS		1/13			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0002321	OMIM:614916	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0011463	PMID:23040497	PCS		3/7			C	HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0006682	PMID:23040497	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0001279	PMID:23040497	PCS		13/13			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0000006	PMID:23040497	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0004756	PMID:23040497	PCS		2/13			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-07-04]
OMIM:614916	Ventricular tachycardia, catecholaminergic polymorphic, 4		HP:0001645	PMID:23040497	PCS		2/13			P	HPO:probinson[2022-07-04];HPO:probinson[2022-07-04]
OMIM:301120	Prostate cancer, susceptibility to		HP:0001417	OMIM:301120	TAS					I	HPO:probinson[2025-02-17]
OMIM:301120	Prostate cancer, susceptibility to		HP:0012125	PMID:10589774	PCS					P	HPO:probinson[2025-02-17]
OMIM:129600	Ectopia lentis, familial		HP:0001166	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		4/37			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000594	PMID:32404357	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0003621	PMID:33576469;PMID:22736615	PCS		3/12			C	HPO:probinson[2021-05-26];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000098	PMID:33576469;PMID:8188302;PMID:22219643;PMID:32404357;PMID:22539873	PCS		1/23			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0003596	PMID:32404357;PMID:22736615	PCS		5/7			C	HPO:probinson[2021-05-26];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000541	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:31527767;PMID:22736615	PCS		7/44			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0002650	PMID:33576469;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		1/31			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000486	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:22736615	PCS		3/30			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0030961	PMID:32404357	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0001382	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		7/37			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0003581	PMID:8188302;PMID:22539873	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0001065	PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		6/29			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0001083	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:15054843;PMID:32404357;PMID:22539873;PMID:22736615;PMID:31527767	PCS		51/57			P	HPO:probinson[2021-05-26];HPO:iea[2009-02-17];HPO:probinson[2021-05-26];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0012773	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		7/37			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0011463	PMID:33576469	PCS		6/8			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0011462	PMID:22736615	PCS		1/4			C	HPO:probinson[2021-05-26]
OMIM:129600	Ectopia lentis, familial		HP:0002616	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:31527767;PMID:22736615	PCS		0/44			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000767	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		3/37			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000218	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		4/37			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000768	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:22539873;PMID:22736615	PCS		1/37			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000006	PMID:15054843;PMID:22736615	PCS		20/20			I	HPO:iea[2009-02-17];HPO:probinson[2021-05-26];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000501	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:31527767;PMID:22736615	PCS		6/43			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0001634	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:22539873;PMID:22736615	PCS		1/31			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:129600	Ectopia lentis, familial		HP:0000545	PMID:33576469;PMID:8188302;PMID:12446365;PMID:22219643;PMID:32404357;PMID:31527767;PMID:22736615	PCS		30/38			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:245010	Haim-Munk syndrome		HP:0001166	OMIM:245010	IEA					P	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0000166	OMIM:245010	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0001805	OMIM:245010	IEA					P	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0009771	OMIM:245010	IEA					P	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0000007	OMIM:245010	IEA					I	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0006224	OMIM:245010	IEA					P	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0007545	OMIM:245010	IEA					P	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0001763	OMIM:245010	IEA					P	HPO:iea[2009-02-17]
OMIM:245010	Haim-Munk syndrome		HP:0005406	OMIM:245010	IEA					P	HPO:iea[2009-02-17]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0003477	PMID:26924529	PCS					P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0003577	OMIM:616867	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0002089	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001371	PMID:26924529	PCS					P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0006829	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001290	OMIM:616867	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0002878	PMID:26924529	PCS					P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0007269	PMID:26924529	PCS					P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001643	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001324	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0002536	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0003447	PMID:26924529	PCS					P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001622	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0003202	PMID:26924529	PCS					P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001561	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0002015	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001263	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001284	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0002804	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0000007	PMID:26924529	PCS					I	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001558	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0002643	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0005855	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0001655	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-20]
OMIM:616867	Spinal muscular atrophy with congenital bone fractures 2		HP:0003557	PMID:26924529	PCS					P	HPO:probinson[2017-06-20]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0002465	PMID:17853471	PCS		4/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0002069	PMID:17853471;PMID:18523455	PCS		3/7			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000340	PMID:17853471	PCS		3/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000582	PMID:18523455	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001212	PMID:17853471	PCS		5/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0004322	PMID:17853471	PCS		2/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000463	PMID:18523455	PCS		2/2			P	HPO:skoehler[2013-05-31];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001250	PMID:10946356	PCS		0/6			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0002121	PMID:17853471	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001252	PMID:17853471	PCS	HP:0011463	3/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001252	PMID:18523455	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0003196	PMID:18523455	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0012368	PMID:18523455	PCS		2/2			P	HPO:skoehler[2013-10-22];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000718	PMID:17853471	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000739	PMID:17853471	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000711	PMID:17853471	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000238	PMID:17853471	PCS		1/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000736	PMID:17853471	PCS		3/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000219	PMID:17853471	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000713	PMID:17853471	PCS		2/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000218	PMID:17853471	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000752	PMID:17853471	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001249	PMID:10946356;PMID:9731525;PMID:12884430;PMID:17853471	PCS		34/34			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000336	PMID:17853471	PCS		2/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001348	PMID:18523455	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000215	PMID:18523455	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000252	PMID:17853471;PMID:18523455	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0002312	PMID:18523455	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000750	PMID:17853471	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0031936	PMID:18523455	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000194	PMID:17853471	PCS		4/5			P	HPO:skoehler[2013-06-04];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000490	PMID:17853471	PCS		2/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001263	PMID:18523455	PCS		2/2			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0002194	PMID:17853471	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000709	PMID:17853471	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0001419	PMID:9731525	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000426	PMID:17853471	PCS		5/5			P	HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0002307	PMID:17853471;PMID:18523455	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300558	Intellectual developmental disorder, X-linked 30		HP:0000400	PMID:12884430;PMID:17853471;PMID:18523455	PCS		13/26			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:241510	Hypophosphatasia, childhood		HP:0000670	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0001363	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0001024	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0004322	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0001250	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0003198	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:6000873	PMID:15782022	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:241510	Hypophosphatasia, childhood		HP:0003282	OMIM:241510	TAS					P	HPO:probinson[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0003491	OMIM:241510	TAS					P	HPO:probinson[2012-05-28]
OMIM:241510	Hypophosphatasia, childhood		HP:0011864	OMIM:241510	TAS					P	HPO:probinson[2012-05-28]
OMIM:241510	Hypophosphatasia, childhood		HP:0002979	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0000007	OMIM:241510	IEA					I	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0002515	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0006323	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0000268	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0002007	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0003239	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0000520	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:241510	Hypophosphatasia, childhood		HP:0000897	OMIM:241510	IEA					P	HPO:iea[2009-02-17]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0004313	PMID:26981933	PCS					P	HPO:probinson[2017-06-20]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0003621	PMID:26981933	PCS		4/19			C	HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0001561	PMID:21548011	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0003596	PMID:26981933	PCS		2/19			C	HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0005387	PMID:26981933	PCS					P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0010976	PMID:26981933	PCS					P	HPO:probinson[2017-06-20]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0011463	PMID:26981933	PCS		7/19			C	HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0011462	PMID:26981933	PCS		6/19			C	HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0002718	PMID:26981933	PCS					P	HPO:probinson[2017-06-20]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0003829	PMID:26981933	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0004429	PMID:26981933	PCS		0/11			P	HPO:probinson[2017-06-20];HPO:probinson[2024-03-15]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0025116	PMID:21548011	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0006721	PMID:26981933	PCS		2/29			P	HPO:probinson[2021-05-09]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0000006	PMID:26981933	PCS					I	HPO:probinson[2017-06-20]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0002841	PMID:26981933	PCS		0/11			P	HPO:probinson[2017-06-20];HPO:probinson[2024-03-15]
OMIM:616873	Immunodeficiency, common variable, 13		HP:0001876	PMID:21548011	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-09]
OMIM:620319	Oocyte/zygote/embryo maturation arrest 17		HP:0008222	PMID:36647821	PCS		10/10			P	HPO:probinson[2023-07-10]
OMIM:620319	Oocyte/zygote/embryo maturation arrest 17		HP:0011462	PMID:36647821	PCS		10/10			C	HPO:probinson[2023-07-10]
OMIM:620319	Oocyte/zygote/embryo maturation arrest 17		HP:0000141	PMID:36647821	PCS		0/10			P	HPO:probinson[2023-07-10]
OMIM:620319	Oocyte/zygote/embryo maturation arrest 17		HP:0000007	PMID:36647821	PCS					I	HPO:probinson[2023-07-10]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003510	PMID:32591345;PMID:36097642;PMID:35427807	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003037	PMID:32591345;PMID:36097642;PMID:35427807	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001176	PMID:32591345;PMID:35427807	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003951	PMID:35427807	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003577	PMID:36097642	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0008905	PMID:32591345;PMID:36097642;PMID:35427807	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001376	PMID:32591345;PMID:36097642;PMID:35427807	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003177	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003097	PMID:32591345;PMID:35427807	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0005792	PMID:32591345;PMID:35427807	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003593	PMID:35427807	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0100864	PMID:32591345;PMID:36097642;PMID:35427807	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0100862	PMID:32591345	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0009185	PMID:35427807	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0002938	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0009882	PMID:35427807	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000316	PMID:32591345;PMID:36097642;PMID:35427807	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001845	PMID:35427807	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001822	PMID:35427807	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001249	PMID:32591345;PMID:36097642;PMID:35427807	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001385	PMID:32591345;PMID:35427807	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000494	PMID:32591345;PMID:36097642;PMID:35427807	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0004379	PMID:35427807	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000431	PMID:32591345;PMID:36097642;PMID:35427807	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0002650	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001288	PMID:32591345;PMID:36097642;PMID:35427807	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000470	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0005121	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0005043	PMID:35427807	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003180	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000926	PMID:32591345;PMID:35427807	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000508	PMID:32591345;PMID:36097642;PMID:35427807	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000904	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000767	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001833	PMID:32591345;PMID:35427807	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0006387	PMID:32591345;PMID:35427807	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0000007	PMID:32591345	PCS					I	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0003956	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0001538	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0002007	PMID:32591345;PMID:36097642;PMID:35427807	PCS		1/6			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:619598	Rhizomelic dysplasia, Ain-Naz type		HP:0002645	PMID:36097642	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-16]
OMIM:600977	Cone-Rod dystrophy 5		HP:0007814	PMID:17377520	PCS					P	HPO:probinson[2022-02-26]
OMIM:600977	Cone-Rod dystrophy 5		HP:0000551	PMID:17377520	PCS					P	HPO:probinson[2013-11-23];HPO:probinson[2022-02-26]
OMIM:600977	Cone-Rod dystrophy 5		HP:0011463	PMID:17377520	PCS					C	HPO:probinson[2022-02-26]
OMIM:600977	Cone-Rod dystrophy 5		HP:0000608	PMID:17377520	PCS					P	HPO:probinson[2013-11-23]
OMIM:600977	Cone-Rod dystrophy 5		HP:0000613	PMID:17377520	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-02-26]
OMIM:600977	Cone-Rod dystrophy 5		HP:0007663	PMID:17377520	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-02-26]
OMIM:600977	Cone-Rod dystrophy 5		HP:0000548	PMID:17377520	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-02-26]
OMIM:600977	Cone-Rod dystrophy 5		HP:0000603	PMID:17377520	PCS					P	HPO:probinson[2022-02-26]
OMIM:600977	Cone-Rod dystrophy 5		HP:0000006	PMID:17377520	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-02-26]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0000486	PMID:39073169	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0002321	PMID:39073169	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001272	PMID:39073169	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001252	PMID:39073169	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001274	PMID:39073169	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001251	PMID:39073169	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0003593	PMID:39073169	PCS		6/8			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001270	PMID:39073169	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0002280	PMID:39073169	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0011220	PMID:39073169	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0011462	PMID:39073169	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0000712	PMID:39073169	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0000736	PMID:39073169	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0003701	PMID:39073169	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0000256	PMID:39073169	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0006956	PMID:39073169	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0000750	PMID:39073169	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001344	PMID:39073169	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0030048	PMID:39073169	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0002451	PMID:39073169	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001263	PMID:39073169	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0034295	PMID:39073169	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0034198	PMID:39073169	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001338	PMID:39073169	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:301134	Intellectual developmental disorder, X-linked 114		HP:0001417	PMID:39073169	PCS					I	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:257400	Nystagmus, congenital motor, autosomal recessive		HP:0006934	OMIM:257400	TAS					P	HPO:skoehler[2015-01-21]
OMIM:257400	Nystagmus, congenital motor, autosomal recessive		HP:0000639	OMIM:257400	TAS					P	HPO:probinson[2009-02-17]
OMIM:257400	Nystagmus, congenital motor, autosomal recessive		HP:0000007	OMIM:257400	IEA					I	HPO:iea[2009-02-17]
OMIM:182290	Smith-Magenis syndrome		HP:0000164	PMID:17539903	PCS		25/46			P	HPO:iea[2010-09-09];HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0004324	PMID:17539903	PCS		10/30			P	HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0010803	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000365	PMID:20932317;PMID:17539903	PCS		52/85			P	HPO:iea[2009-02-17];HP:probinson[2019-06-12];ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000321	PMID:20932317	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000486	PMID:20932317	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0004322	PMID:1746552;PMID:20932317;PMID:17539903	PCS		57/77			P	HPO:iea[2010-09-09];HP:probinson[2019-06-12];ORCID:0000-0002-0736-9199[2024-06-18];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001250	PMID:1746552;PMID:17539903	PCS		27/104			P	HPO:iea[2010-09-09];HP:probinson[2019-06-12];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0008609	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001252	PMID:20932317	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000283	PMID:20932317;PMID:20301487	PCS		7/12			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002020	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0001290	PMID:20301487	PCS	HP:0003593	HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0011342	PMID:20932317	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0001609	PMID:20932317;PMID:17539903;PMID:20301487	PCS		68/84			P	HPO:iea[2009-02-17];HP:probinson[2019-06-12];ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0011220	PMID:1746552	PCS		16/26			P	HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0005607	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000356	OMIM:182290	TAS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000752	PMID:17539903	PCS		49/66			P	HPO:iea[2009-02-17];HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0003745	PMID:20301487	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001169	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002019	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001763	PMID:1746552;PMID:20932317	PCS		12/20			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002973	PMID:20301487	PCS		HP:0040283			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001249	PMID:20932317	PCS		2/2			P	HPO:skoehler[2013-01-22]
OMIM:182290	Smith-Magenis syndrome		HP:0000478	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001600	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0007328	OMIM:182290	TAS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0003623	PMID:20932317	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0001265	PMID:1746552	PCS		10/16			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002353	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002155	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0003124	PMID:17539903	PCS		7/17			P	HPO:iea[2010-09-09];HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0000490	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001263	PMID:17539903	PCS		105/105			P	HPO:iea[2010-09-09];HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0011800	PMID:20932317	PCS		2/2			P	HPO:skoehler[2013-11-28]
OMIM:182290	Smith-Magenis syndrome		HP:0032521	PMID:17539903	PCS					P	HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0002108	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0004209	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000202	PMID:20301487	PCS		HP:0040283			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000006	PMID:17539903	PCS					I	HPO:iea[2010-09-09];HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0000248	PMID:20932317;PMID:20301487	PCS		7/12			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000220	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000582	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000541	PMID:20301487	PCS		HP:0040283			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001156	PMID:1746552;PMID:20932317	PCS		22/27			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0031849	PMID:11445803	PCS					P	HPO:lccarmody[2018-09-25]
OMIM:182290	Smith-Magenis syndrome		HP:0002121	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0004220	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0002360	PMID:20932317;PMID:17539903	PCS		46/52			P	HPO:iea[2009-02-17];HP:probinson[2019-06-12];ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0001270	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0012210	OMIM:182290	TAS					P	HPO:skoehler[2012-10-17]
OMIM:182290	Smith-Magenis syndrome		HP:0001508	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0007021	PMID:1746552	PCS		8/16			P	HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002715	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0030680	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000733	PMID:17539903	PCS		35/59			P	HPO:iea[2010-09-09];HP:probinson[2019-06-12]
OMIM:182290	Smith-Magenis syndrome		HP:0000733	PMID:20301487	PCS	HP:0003593	HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001627	OMIM:182290	TAS					P	HPO:skoehler[2015-12-30]
OMIM:182290	Smith-Magenis syndrome		HP:0002119	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002714	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000079	PMID:20301487	PCS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000750	PMID:20932317;PMID:20301487	PCS		7/12			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0002650	PMID:1746552;PMID:20932317;PMID:17539903	PCS		38/108			P	HPO:iea[2009-02-17];HP:probinson[2019-06-12];ORCID:0000-0002-0736-9199[2024-06-18];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0004279	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000431	PMID:1746552	PCS		23/26			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0032508	PMID:20932317	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:182290	Smith-Magenis syndrome		HP:0032509	PMID:20932317	PCS		1/2			P	HPO:skoehler[2019-09-07]
OMIM:182290	Smith-Magenis syndrome		HP:0001284	OMIM:182290	TAS					P	HPO:skoehler[2013-01-22]
OMIM:182290	Smith-Magenis syndrome		HP:0000272	PMID:1746552	PCS		24/26			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000708	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0012168	PMID:20932317	PCS		1/2			P	HPO:skoehler[2013-02-25];HPO:probinson[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0010780	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0009830	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0001956	PMID:20932317	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0040129	PMID:1746552	PCS		0/11			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000389	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000664	PMID:20932317;PMID:20301487	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-06-18];HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000820	PMID:20301487	PCS		HP:0040282			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000303	PMID:1746552	PCS	HP:0003584	15/26			P	HPO:iea[2010-09-09];HPO:probinson[2024-03-08]
OMIM:182290	Smith-Magenis syndrome		HP:0000303	PMID:20932317	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000545	PMID:20932317	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-18]
OMIM:182290	Smith-Magenis syndrome		HP:0000742	PMID:17539903	PCS		77/86			P	HPO:iea[2010-09-09];HP:probinson[2019-06-12]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0003577	PMID:31312705;PMID:31302245	PCS		3/3			C	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0000365	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0004057	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0001263	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0003819	PMID:31312705	PCS		1/1			C	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0008066	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0008066	PMID:31302245	PCS	HP:0003577	2/2			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0100806	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0000007	PMID:31312705	PCS					I	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0000768	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0002788	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0001522	PMID:31302245	PCS		1/2			C	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0001510	PMID:31312705	PCS		1/1			P	HPO:probinson[2021-11-13]
OMIM:619599	Epidermolysis bullosa simplex 2D, generalized, intermediate or severe, autosomal recessive		HP:0200097	PMID:31312705;PMID:31302245	PCS		3/3			P	HPO:probinson[2021-11-13]
OMIM:609952	Deafness, autosomal recessive 55		HP:0000365	PMID:16098016	PCS	HP:0003593	4/4			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-14]
OMIM:609952	Deafness, autosomal recessive 55		HP:0001751	PMID:16098016	PCS		0/4			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-14]
OMIM:609952	Deafness, autosomal recessive 55		HP:0000007	PMID:16098016	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:609952	Deafness, autosomal recessive 55		HP:0007663	PMID:16098016	PCS		0/4			P	HPO:probinson[2024-03-14]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0000252	PMID:31607425	PCS		2/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0002133	PMID:31607425	PCS		3/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0001344	PMID:31607425	PCS		2/5			P	HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0004322	PMID:31607425	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0031936	PMID:31607425	PCS		3/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0001250	PMID:31607425	PCS		3/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0002066	PMID:31607425	PCS		1/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0001263	PMID:31607425	PCS		5/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0001290	PMID:31607425	PCS		5/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0001270	PMID:31607425	PCS		5/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0000718	PMID:31607425	PCS		3/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0000007	PMID:31607425	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0000505	PMID:31607425	PCS		1/5			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618687	Intellectual developmental disorder with short stature and behavioral abnormalities		HP:0007018	PMID:31607425	PCS		3/5			P	HPO:probinson[2020-06-27]
OMIM:106190	Anhidrosis, isolated, with normal sweat glands		HP:0001595	PMID:25329695	PCS		0/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-23]
OMIM:106190	Anhidrosis, isolated, with normal sweat glands		HP:0002046	PMID:25329695	PCS		5/5			P	HPO:skoehler[2012-08-05];HPO:probinson[2022-09-23]
OMIM:106190	Anhidrosis, isolated, with normal sweat glands		HP:0001507	PMID:25329695	PCS		0/5			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-23]
OMIM:106190	Anhidrosis, isolated, with normal sweat glands		HP:0000007	PMID:25329695	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-23]
OMIM:106190	Anhidrosis, isolated, with normal sweat glands		HP:0007459	PMID:25329695	PCS		5/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-23]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0005535	OMIM:194380	IEA					P	HPO:iea[2009-02-17]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0000980	OMIM:194380	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0003641	OMIM:194380	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0002240	OMIM:194380	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0001081	OMIM:194380	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0003281	OMIM:194380	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0012115	OMIM:194380	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0032106	OMIM:194380	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0025548	OMIM:194380	IEA					P	HPO:skoehler[2018-10-08]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0008269	OMIM:194380	IEA					P	HPO:iea[2009-02-17]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0001923	OMIM:194380	TAS					P	HPO:skoehler[2013-07-30]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0000006	OMIM:194380	TAS					I	HPO:iea[2009-02-17]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0000952	OMIM:194380	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194380	Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema		HP:0001744	OMIM:194380	TAS		HP:0040283			P	HPO:skoehler[2013-07-30]
OMIM:600962	Palmoplantar keratoderma, nonepidermolytic		HP:0003577	PMID:7528239	PCS					C	HPO:probinson[2021-05-02]
OMIM:600962	Palmoplantar keratoderma, nonepidermolytic		HP:0000006	PMID:7528239	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:600962	Palmoplantar keratoderma, nonepidermolytic		HP:0007404	PMID:7528239	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:176305	Preaxial deficiency, postaxial polydactyly, and hypospadias		HP:0000807	PMID:11968094	PCS		2/2	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:176305	Preaxial deficiency, postaxial polydactyly, and hypospadias		HP:0001162	PMID:11968094	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:176305	Preaxial deficiency, postaxial polydactyly, and hypospadias		HP:0009237	PMID:11968094	PCS					P	HPO:probinson[2023-05-19]
OMIM:176305	Preaxial deficiency, postaxial polydactyly, and hypospadias		HP:0001885	PMID:11968094	PCS		3/3			P	HPO:probinson[2013-04-07];HPO:probinson[2023-05-19]
OMIM:176305	Preaxial deficiency, postaxial polydactyly, and hypospadias		HP:0009778	PMID:11968094	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-19]
OMIM:176305	Preaxial deficiency, postaxial polydactyly, and hypospadias		HP:0000006	PMID:11968094	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0003577	OMIM:162370	TAS					C	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0002136	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0006903	OMIM:162370	IEA					P	HPO:iea[2009-02-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0003487	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0031936	OMIM:162370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0003693	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0003680	OMIM:162370	TAS					C	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0002460	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0001848	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0002804	OMIM:162370	IEA					P	HPO:iea[2009-02-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0003307	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0003701	OMIM:162370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0001257	OMIM:162370	TAS					P	HPO:skoehler[2015-12-30]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0000006	OMIM:162370	IEA					I	HPO:iea[2009-02-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0002522	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162370	Neuropathy, congenital, with arthrogryposis multiplex		HP:0002600	OMIM:162370	TAS					P	HPO:skoehler[2012-10-17]
OMIM:190680	Triphalangeal thumbs with brachyectrodactyly		HP:0001199	OMIM:190680	IEA					P	HPO:iea[2009-02-17]
OMIM:190680	Triphalangeal thumbs with brachyectrodactyly		HP:0005643	OMIM:190680	IEA					P	HPO:iea[2009-02-17]
OMIM:190680	Triphalangeal thumbs with brachyectrodactyly		HP:0001156	OMIM:190680	IEA					P	HPO:skoehler[2018-10-08]
OMIM:190680	Triphalangeal thumbs with brachyectrodactyly		HP:0001839	OMIM:190680	TAS					P	HPO:probinson[2009-02-17]
OMIM:190680	Triphalangeal thumbs with brachyectrodactyly		HP:0001171	OMIM:190680	TAS					P	HPO:probinson[2009-02-17]
OMIM:190680	Triphalangeal thumbs with brachyectrodactyly		HP:0009536	OMIM:190680	TAS					P	HPO:probinson[2012-06-08]
OMIM:190680	Triphalangeal thumbs with brachyectrodactyly		HP:0000006	OMIM:190680	IEA					I	HPO:iea[2009-02-17]
OMIM:114580	Candidiasis, familial chronic mucocutaneous, autosomal dominant		HP:0000818	OMIM:114580	IEA					P	HPO:iea[2009-02-17]
OMIM:114580	Candidiasis, familial chronic mucocutaneous, autosomal dominant		HP:0001596	OMIM:114580	IEA					P	HPO:iea[2009-02-17]
OMIM:114580	Candidiasis, familial chronic mucocutaneous, autosomal dominant		HP:0006480	OMIM:114580	TAS					P	HPO:skoehler[2009-02-17]
OMIM:114580	Candidiasis, familial chronic mucocutaneous, autosomal dominant		HP:0002728	OMIM:114580	IEA					P	HPO:iea[2009-02-17]
OMIM:114580	Candidiasis, familial chronic mucocutaneous, autosomal dominant		HP:0004429	OMIM:114580	IEA					P	HPO:iea[2009-02-17]
OMIM:114580	Candidiasis, familial chronic mucocutaneous, autosomal dominant		HP:0002965	OMIM:114580	IEA					P	HPO:iea[2009-02-17]
OMIM:114580	Candidiasis, familial chronic mucocutaneous, autosomal dominant		HP:0000006	OMIM:114580	IEA					I	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000066	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000143	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0001374	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0002023	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0002144	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0008707	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000061	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000081	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0010305	OMIM:258040	TAS					P	HPO:skoehler[2013-10-22]
OMIM:258040	OEIS complex		HP:0008490	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0002937	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0002836	OMIM:258040	IEA					P	HPO:skoehler[2015-01-21]
OMIM:258040	OEIS complex		HP:0000238	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000878	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000136	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0003745	OMIM:258040	IEA					I	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000039	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0001545	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000033	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000054	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0001586	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0001762	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0002475	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0005223	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000072	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0010475	OMIM:258040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:258040	OEIS complex		HP:0002308	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0001539	OMIM:258040	TAS					P	HPO:probinson[2009-02-17]
OMIM:258040	OEIS complex		HP:0000125	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000028	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0002566	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000104	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:258040	OEIS complex		HP:0000126	OMIM:258040	IEA					P	HPO:iea[2009-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0002983	PMID:11180245;PMID:18382993;PMID:14684697	PCS		4/7			P	HPO:probinson[2021-11-24];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0002101	OMIM:215140	TAS		1/1			P	HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0005257	PMID:14684697	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:215140	Greenberg skeletal dysplasia		HP:0012789	PMID:12210303	PCS		1/1			P	HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0010049	PMID:8213919	PCS		1/1			P	HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0010766	PMID:18382993	PCS		1/3			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0009381	PMID:3377005	PCS		1/2			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0008890	PMID:11113916	PCS		1/1			P	HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0011461	PMID:11180245;PMID:12210303	PCS		2/2			C	HPO:probinson[2022-02-17];HPO:probinson[2022-04-24]
OMIM:215140	Greenberg skeletal dysplasia		HP:0100603	PMID:3377005	PCS		1/2			H	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0005807	PMID:8213919	PCS		1/1			P	HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000316	PMID:18382993;PMID:14684697	PCS		2/5			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0003826	PMID:12618959;PMID:12210303	PCS		2/2			C	HPO:skoehler[2014-03-24];HPO:probinson[2022-02-17];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000878	PMID:11113916;PMID:12210303	PCS		2/2			P	HPO:probinson[2022-02-17];HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0005528	PMID:3377005	PCS					P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001169	PMID:11180245;PMID:12210303	PCS		2/3			P	HPO:probinson[2022-02-17];HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000476	PMID:8213919;PMID:12210303	PCS		2/2			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000278	PMID:14684697	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000890	PMID:8213919	PCS		1/1			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0003440	PMID:12210303	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0006619	PMID:11180245	PCS		1/1			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0004331	PMID:3377005;PMID:8213919;PMID:14684697	PCS		3/5			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0011800	PMID:11180245;PMID:3377005;PMID:8213919;PMID:12210303	PCS		4/5			P	HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0041159	PMID:18382993	PCS		1/3			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0010880	PMID:14684697	PCS		1/2			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000926	OMIM:215140;PMID:11180245;PMID:3377005;PMID:8213919;PMID:14684697	PCS		17/17			P	HPO:probinson[2021-11-24];HPO:probinson[2012-07-25];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000327	PMID:8213919;PMID:12210303	PCS		2/3			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000007	PMID:12618959	PCS					I	HPO:probinson[2024-08-03]
OMIM:215140	Greenberg skeletal dysplasia		HP:0006267	PMID:18382993	PCS		1/3			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001538	PMID:3377005;PMID:14684697	PCS		4/5			P	HPO:probinson[2022-02-17];HPO:probinson[2022-02-17];HPO:probinson[2021-11-24];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000369	PMID:18382993	PCS		11/13			P	HPO:iea[2012-07-25];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0005019	PMID:8213919	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0005855	PMID:14684697	PCS		1/2			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0002787	PMID:8213919	PCS		1/1			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0003015	PMID:3377005	PCS		11/12			P	HPO:iea[2012-07-25];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0002089	PMID:12210303	PCS		1/3			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0008905	PMID:3377005;PMID:8213919;PMID:18382993;PMID:14684697	PCS		7/7			P	HPO:probinson[2021-11-24];HP:probinson[2022-02-17];HPO:probinson[2022-02-17];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000782	PMID:11180245	PCS					P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001552	PMID:11180245;PMID:8213919	PCS		2/2			P	HPO:probinson[2022-02-17];HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001156	PMID:3377005;PMID:8213919	PCS		2/3			P	HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0030674	PMID:14684697	PCS		1/1			C	HPO:probinson[2021-11-24]
OMIM:215140	Greenberg skeletal dysplasia		HP:0002240	PMID:18382993;PMID:14684697	PCS		4/5			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001790	PMID:11113916;PMID:12618959	PCS		2/2			P	HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0010943	PMID:14684697	PCS		2/3			P	HPO:probinson[2021-11-24];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0009487	PMID:12210303	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0008873	PMID:3377005;PMID:8213919;PMID:12618959	PCS		3/4			P	HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001789	PMID:11180245;PMID:8213919;PMID:18382993;PMID:14684697	PCS		7/8			P	HPO:probinson[2021-11-24];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0008479	PMID:3377005	PCS		1/2			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0008754	PMID:14684697	PCS		2/2			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0002757	PMID:14684697	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000774	PMID:11180245;PMID:3377005;PMID:18382993;PMID:14684697	PCS		7/8			P	HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000256	PMID:18382993	PCS		1/3			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000773	PMID:11180245;PMID:8213919;PMID:12618959	PCS		3/3			P	HPO:probinson[2022-02-17];HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000457	PMID:14684697;PMID:12210303	PCS		3/4			P	HPO:probinson[2021-11-24];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000336	PMID:12210303	PCS		1/1			P	HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0009803	PMID:3377005	PCS					P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0006559	PMID:18382993	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0003026	PMID:11180245;PMID:18382993;PMID:14684697	PCS		7/7			P	HPO:probinson[2021-11-24];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0004599	PMID:3377005	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0003027	PMID:8213919;PMID:12210303	PCS		2/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-02-17];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001561	PMID:3377005;PMID:12210303	PCS		2/3			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0006637	PMID:3377005	PCS					P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0030721	PMID:11113916	PCS	HP:0011461	1/1			P	HPO:probinson[2022-01-29]
OMIM:215140	Greenberg skeletal dysplasia		HP:0004510	PMID:3377005	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0002694	PMID:11180245;PMID:8213919;PMID:12210303	PCS		3/4			P	HPO:probinson[2022-02-17];HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0004598	PMID:12210303	PCS		1/2			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001883	PMID:14684697	PCS		1/2			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0010659	OMIM:215140	IEA					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001162	PMID:8213919;PMID:14684697;PMID:12618959	PCS		4/5			P	HPO:probinson[2021-11-24];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0003021	PMID:12210303	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0011986	PMID:18382993	PCS		1/3			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0005280	PMID:18382993	PCS		1/3			P	HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0010655	PMID:14684697	PCS		1/2			P	HPO:iea[2012-07-30];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0008420	PMID:18382993	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000348	PMID:14684697	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0006640	PMID:14684697	PCS		3/3			P	HPO:probinson[2021-11-24];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0005716	PMID:14684697	PCS					P	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0003811	PMID:14684697	PCS					C	HPO:iea[2012-07-25]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001830	PMID:18382993;PMID:14684697	PCS		1/4			P	HPO:probinson[2021-11-24];HPO:iea[2012-07-25];HPO:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0001433	PMID:11113916	PCS		1/1			P	HPO:iea[2012-07-25];HPO:probinson[2022-01-29]
OMIM:215140	Greenberg skeletal dysplasia		HP:0008747	PMID:14684697	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:215140	Greenberg skeletal dysplasia		HP:0000347	PMID:3377005;PMID:14684697	PCS		2/4			P	HPO:iea[2012-07-25];HPO:probinson[2022-02-17];HP:probinson[2022-02-17]
OMIM:215140	Greenberg skeletal dysplasia		HP:0006646	PMID:14684697	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:609946	Deafness, autosomal recessive 47		HP:0000365	PMID:16261342	PCS	HP:0003593	5/5			P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:609946	Deafness, autosomal recessive 47		HP:0001751	PMID:16261342	PCS		0/5			P	HP:probinson[2019-03-02];HPO:probinson[2024-03-14]
OMIM:609946	Deafness, autosomal recessive 47		HP:0000007	PMID:16261342	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:609946	Deafness, autosomal recessive 47		HP:0007663	PMID:16261342	PCS		0/5			P	HPO:probinson[2024-03-14]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003202	OMIM:300559	IEA					P	HPO:iea[2009-02-17]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003236	PMID:15637709;OMIM:300559	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20];HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003731	PMID:15637709	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:6000198	PMID:15637709	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003596	PMID:7874115;PMID:15637709	PCS		3/3			C	HPO:probinson[2022-07-20];HPO:probinson[2024-02-27]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003693	PMID:7874115	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0030231	PMID:7874115	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0002460	PMID:7874115	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0009051	PMID:15637709	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0001419	PMID:7874115	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0007340	PMID:7874115	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003738	OMIM:300559	IEA					P	HPO:iea[2009-02-17]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003749	PMID:15637709	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0001943	PMID:7874115	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0001324	OMIM:300559	IEA					P	HPO:iea[2009-02-17]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0008305	OMIM:300559	IEA					P	HPO:iea[2009-02-17]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003713	PMID:7874115	PCS		1/1			P	HPO:probinson[2022-07-20]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0008967	OMIM:300559	IEA					P	HPO:iea[2009-02-17]
OMIM:300559	Muscle glycogenosis, X-linked		HP:0003546	OMIM:300559	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-20]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0003477	PMID:26924529	PCS					P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0003577	OMIM:616866	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0002089	PMID:26924529	PCS		2/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001371	PMID:26924529	PCS					P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0000160	PMID:26924529	PCS		2/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0006829	PMID:26924529	PCS		5/5			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0100295	PMID:26924529	PCS		3/3			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001290	OMIM:616866	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0000316	PMID:26924529	PCS		3/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0000218	PMID:26924529	PCS		3/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0007269	OMIM:616866	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001324	PMID:26924529	PCS		4/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001643	PMID:26924529	PCS		3/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0003700	PMID:26924529	PCS					P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001622	PMID:26924529	PCS		2/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0003447	OMIM:616866	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001562	PMID:26924529	PCS		3/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0002015	PMID:26924529	PCS		4/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001684	PMID:26924529	PCS		2/6			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001263	PMID:26924529	PCS		4/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001284	PMID:26924529	PCS		2/2			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0009110	PMID:26924529	PCS					P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0000308	PMID:26924529	PCS		4/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0002804	PMID:26924529	PCS		6/6			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0000007	PMID:26924529	PCS					I	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001635	PMID:26924529	PCS		1/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001558	PMID:26924529	PCS	HP:0011461	4/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001638	PMID:26924529	PCS		2/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0000966	PMID:26924529	PCS		3/6			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0002643	PMID:26924529	PCS		5/5			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0003557	PMID:26924529	PCS		3/3			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0005855	PMID:26924529	PCS		3/4			P	HPO:probinson[2017-06-19]
OMIM:616866	Spinal muscular atrophy with congenital bone fractures 1		HP:0001655	PMID:26924529	PCS	HP:0003577	1/4			P	HPO:probinson[2017-06-19]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000044	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0002025	PMID:17431922	PCS		2/6			P	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0009937	PMID:17431922	PCS		2/5			P	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001770	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000365	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0003593	PMID:17431922	PCS		2/6			C	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001171	PMID:17431922	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000081	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0045075	PMID:17431922	PCS		1/6			P	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0011463	PMID:17431922	PCS		3/6			C	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000635	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000437	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001803	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001249	OMIM:604292	TAS		7%			P	HPO:probinson[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0002215	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000175	PMID:17431922	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000054	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000453	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000691	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0100257	OMIM:604292	TAS					P	HPO:iea[2015-12-30]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001739	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000968	OMIM:604292	TAS					P	HPO:probinson[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000327	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0008404	PMID:10535733	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2020-09-12]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0007513	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0007678	PMID:17431922	PCS		6/6			P	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000006	PMID:10535733	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000204	PMID:17431922	PCS		0/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0002225	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000126	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000962	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000021	OMIM:604292	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0003577	PMID:17431922	PCS		1/6			C	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000145	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0002286	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000581	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001592	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0008551	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000613	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000217	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000015	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0002557	PMID:17431922	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000653	PMID:17431922	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000498	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001545	PMID:17431922	PCS		2/6			P	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000198	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000110	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000670	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000076	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000072	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000272	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0004590	PMID:17431922	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000070	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0001839	PMID:17431922	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0008661	OMIM:604292	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0002209	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000824	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000620	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000028	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000863	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:604292	Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3		HP:0000104	OMIM:604292	IEA					P	HPO:iea[2009-02-17]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0000253	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0009904	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0000175	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0001583	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0000750	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0030147	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0001310	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0001260	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0001270	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0003391	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0008167	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0000007	PMID:27799409	PCS					I	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0000601	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0002515	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0003429	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0002527	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0003701	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0000510	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618863	Retinal dystrophy with leukodystrophy		HP:0001488	PMID:27799409	PCS		1/1			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:178300	Ptosis, hereditary congenital 1		HP:0007970	OMIM:178300	IEA					P	HPO:iea[2009-02-17]
OMIM:178300	Ptosis, hereditary congenital 1		HP:0000006	OMIM:178300	IEA					I	HPO:iea[2009-02-17]
OMIM:620442	Breast-ovarian cancer, familial, susceptibility to, 5		HP:0003002	PMID:17200668;PMID:22241545	PCS		15/1488			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:620442	Breast-ovarian cancer, familial, susceptibility to, 5		HP:0000006	PMID:17200668	PCS					I	HPO:probinson[2024-03-02]
OMIM:167220	Pacman dysplasia		HP:0006487	OMIM:167220	IEA					P	HPO:skoehler[2010-06-18]
OMIM:167220	Pacman dysplasia		HP:0005716	OMIM:167220	IEA					P	HPO:iea[2009-02-17]
OMIM:167220	Pacman dysplasia		HP:0000006	OMIM:167220	IEA					I	HPO:iea[2009-02-17]
OMIM:167220	Pacman dysplasia		HP:0010655	OMIM:167220	IEA					P	HPO:iea[2009-02-17]
OMIM:600792	Deafness, neurosensory, autosomal recessive 5		HP:0000407	OMIM:600792	TAS					P	HPO:skoehler[2010-06-18]
OMIM:600792	Deafness, neurosensory, autosomal recessive 5		HP:0000007	OMIM:600792	TAS					I	HPO:skoehler[2009-02-17]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001890	PMID:37342957	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001252	PMID:37342957	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0003593	PMID:37342957	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0011463	PMID:36952639;PMID:37342957	PCS		3/12			C	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0008897	PMID:36952639	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0004315	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0025379	PMID:36952639	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0020086	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0032564	PMID:36952639	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0031234	PMID:36952639	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001419	PMID:36952639	PCS					I	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0000403	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001973	PMID:36952639	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0004844	PMID:36952639	PCS		4/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001974	PMID:37342957	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0007417	PMID:36952639;PMID:37342957	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0003577	PMID:37342957	PCS		1/4			C	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0000100	PMID:36952639;PMID:37342957	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0000265	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0003212	PMID:37342957	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0003493	PMID:36952639;PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002240	PMID:37342957	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:4000031	PMID:36952639	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0031123	PMID:37342957	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0033028	PMID:36952639	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:4000025	PMID:36952639	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001904	PMID:36952639	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001508	PMID:37342957	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001701	PMID:36952639	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002837	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0012490	PMID:36952639;PMID:37342957	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0006532	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0001744	PMID:37342957	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002014	PMID:36952639;PMID:37342957	PCS		3/12			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002850	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0003621	PMID:36952639	PCS		6/8			C	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0005764	PMID:36952639	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0000155	PMID:36952639	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0000474	PMID:37342957	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0100280	PMID:37342957	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0003262	PMID:36952639;PMID:37342957	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0032069	PMID:36952639	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0033677	PMID:36952639;PMID:37342957	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002091	PMID:36952639	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0011273	PMID:37342957	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0100279	PMID:36952639;PMID:37342957	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0032230	PMID:36952639;PMID:37342957	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002725	PMID:36952639;PMID:37342957	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002923	PMID:36952639	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:301109	Autoinflammatory disease, multisystem, with immune dysregulation, X-linked		HP:0002720	PMID:36952639;PMID:37342957	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-12]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0000252	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0000365	OMIM:309555	TAS		20/20		HP:0012828	P	HPO:probinson[2009-02-17];HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0001250	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0003819	OMIM:309555	TAS					C	HPO:probinson[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0000618	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0001141	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0000648	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0001417	OMIM:309555	IEA					I	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0005193	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0001257	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:309555	Intellectual developmental disorder, X-linked syndromic, Gustavson type		HP:0001249	OMIM:309555	IEA					P	HPO:iea[2009-02-17]
OMIM:302400	Central incisors, absence of		HP:0006289	OMIM:302400	IEA					P	HPO:iea[2009-02-17]
OMIM:302400	Central incisors, absence of		HP:0001417	OMIM:302400	IEA					I	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0000252	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0003023	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0000592	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0005474	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0002691	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0000519	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0000767	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0003826	OMIM:259410	TAS					C	HPO:skoehler[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0008873	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0000007	OMIM:259410	IEA					I	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0000768	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0002645	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0000963	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:259410	Osteogenesis imperfecta congenita, microcephaly, and cataracts		HP:0005855	OMIM:259410	IEA					P	HPO:iea[2009-02-17]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0012132	PMID:15459009	PCS		1/1			P	HPO:probinson[2023-03-29]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0025066	PMID:15459009	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-29]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0012465	PMID:15459009	PCS		1/1			P	HPO:probinson[2023-03-29]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0001903	PMID:15459009	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0003452	PMID:15459009	PCS		1/1			P	HPO:probinson[2023-03-29]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0032231	PMID:15459009	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-29]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0003593	PMID:15459009	PCS		1/1			C	HPO:probinson[2023-03-29]
OMIM:206100	Anemia, hypochromic microcytic, with iron overload 1		HP:0000007	PMID:15459009	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-29]
OMIM:620456	Dystonia 22, adult-onset		HP:0000473	PMID:33539324	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0003596	PMID:33539324	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0001288	PMID:33539324	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0003487	PMID:33539324	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0007351	PMID:33539324	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0003584	PMID:33539324	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0004373	PMID:33539324	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0000007	PMID:33539324	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0001270	PMID:33539324	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0001268	PMID:33539324	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620456	Dystonia 22, adult-onset		HP:0002544	PMID:33539324	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:254120	Muscular hypertonia, lethal		HP:0001276	OMIM:254120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254120	Muscular hypertonia, lethal		HP:0003577	PMID:4426128	PCS		7/7			C	HPO:probinson[2022-07-01]
OMIM:254120	Muscular hypertonia, lethal		HP:0002375	OMIM:254120	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254120	Muscular hypertonia, lethal		HP:0002098	PMID:4426128	PCS					P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:254120	Muscular hypertonia, lethal		HP:0001537	PMID:4426128	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:254120	Muscular hypertonia, lethal		HP:0000007	OMIM:254120	IEA					I	HPO:iea[2009-02-17]
OMIM:254120	Muscular hypertonia, lethal		HP:0001558	PMID:4426128	PCS					P	HPO:skoehler[2014-04-13];HPO:probinson[2022-07-01]
OMIM:254120	Muscular hypertonia, lethal		HP:0002090	OMIM:254120	IEA					P	HPO:iea[2009-02-17]
OMIM:254120	Muscular hypertonia, lethal		HP:0001522	PMID:4426128	PCS		7/7			C	HPO:probinson[2022-07-01]
OMIM:254120	Muscular hypertonia, lethal		HP:0100660	OMIM:254120	IEA					P	HPO:skoehler[2018-10-08]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0002521	PMID:24011988	PCS		3/14			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0000252	PMID:24011988	PCS		7/14			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0002188	PMID:24011988	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0002156	PMID:24011988	PCS		HP:0040283			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0004322	OMIM:309541	TAS					P	HPO:skoehler[2012-11-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0001266	PMID:24011988	PCS		4/14			P	HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0030674	PMID:24011988	PCS		3/14			C	HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0001250	PMID:24011988	PCS		9/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0001252	PMID:24011988	PCS		3/14			P	HPO:skoehler[2014-11-26]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0001263	PMID:24011988	PCS		12/14			P	HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0003593	PMID:24011988	PCS		10/14			C	HPO:skoehler[2013-11-18]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0002072	PMID:24011988	PCS		1/14			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0002160	PMID:24011988	PCS		5/10			P	HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0012469	PMID:24011988	PCS		3/14			P	HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0001508	PMID:24011988	PCS		5/14			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0001419	PMID:23000143	PCS					I	HPO:skoehler[2012-11-25];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0012120	PMID:24011988	PCS		11/11			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0002912	PMID:24011988	PCS		7/7			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0002305	PMID:24011988	PCS		HP:0040283			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0000248	OMIM:309541	TAS					P	HPO:skoehler[2012-11-25]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0001249	OMIM:309541	TAS					P	HPO:probinson[2009-02-17]
OMIM:309541	Methylmalonic acidemia and homocysteinemia, Cblx type		HP:0003623	PMID:24011988	PCS		1/14			C	HPO:probinson[2023-02-25]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001276	PMID:32197074	PCS		8/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002540	PMID:32197074	PCS		3/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002067	PMID:32197074	PCS		3/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002188	PMID:32197074	PCS		2/2			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001332	PMID:32197074	PCS		4/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001250	PMID:32197074	PCS		4/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002066	PMID:32197074	PCS		4/7			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001252	PMID:32197074	PCS		7/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002063	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0000020	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0003593	PMID:32197074	PCS					C	HPO:probinson[2022-03-14]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0100248	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002599	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002578	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0000252	PMID:32197074	PCS		2/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002059	PMID:32197074	PCS					P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001344	PMID:32197074	PCS		3/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002078	PMID:32197074	PCS		3/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001300	PMID:32197074	PCS		4/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001266	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0000298	PMID:32197074	PCS		2/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002079	PMID:32197074	PCS					P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001260	PMID:32197074	PCS		6/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002607	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001257	PMID:32197074	PCS		7/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0000006	PMID:32197074	PCS					I	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001337	PMID:32197074	PCS		3/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0002126	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:618877	Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome		HP:0001336	PMID:32197074	PCS		1/9			P	HPO:probinson[2020-06-23]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0001892	PMID:10891444;PMID:7363509	PCS		23/23			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14];HPO:probinson[2009-02-17];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0003577	PMID:10891444	IEA		5/13			C	HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0030137	PMID:7363509	PCS		3/6			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0003593	PMID:10891444	PCS		4/13			C	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0011900	OMIM:202400	TAS					P	HPO:probinson[2013-03-11];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0011421	PMID:7363509	PCS		1/10			C	HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0100310	PMID:7363509	PCS		1/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0011884	PMID:7363509	PCS		4/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0012223	PMID:7363509	PCS		2/10			P	HPO:probinson[2013-03-30];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0003819	PMID:7363509	PCS		3/10			C	HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0034287	PMID:7363509;PMID:10891444	PCS		23/23			P	HPO:probinson[2022-06-04]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0011463	PMID:10891444	PCS		4/13			C	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0006298	PMID:7363509	PCS		1/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0000007	PMID:10891444	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0000978	PMID:7363509	PCS		1/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0100309	PMID:7363509	PCS		1/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0001934	PMID:7363509	PCS		1/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0001522	PMID:7363509	IEA		2/10			C	HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0003811	PMID:7363509	PCS		2/10			C	HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0000421	PMID:7363509	PCS		3/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0000225	PMID:7363509	PCS		2/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:202400	Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included		HP:0002248	PMID:7363509	PCS		1/10			P	HPO:probinson[2022-05-14];HPO:probinson[2022-05-14]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002465	OMIM:616682	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000384	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0003577	PMID:26246518	PCS		2/4			C	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000486	PMID:26246518	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002164	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001250	PMID:26246518	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001252	PMID:26246518	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002580	PMID:26246518	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002020	OMIM:616682	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0003593	PMID:26246518;OMIM:616682	PCS		11/14			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0040183	PMID:26246518	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000280	OMIM:616682	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001270	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0008070	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001629	PMID:26246518	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0011463	PMID:26246518	PCS		1/4			C	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000316	PMID:26246518	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001845	PMID:26246518	PCS		2/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000414	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000733	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002317	PMID:26246518	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001643	OMIM:616682	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002019	OMIM:616682	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000256	PMID:26246518	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001763	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001342	PMID:26246518	PCS		2/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002036	PMID:26246518	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0005326	OMIM:616682	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000252	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002650	PMID:26246518	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0011968	PMID:26246518	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0001263	PMID:26246518	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000093	PMID:26246518	PCS		2/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0010535	PMID:26246518	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000826	PMID:26246518	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000729	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000007	PMID:26246518	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0004209	OMIM:616682	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002505	PMID:26246518	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0000028	PMID:26246518	PCS		3/3	MALE		P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0002566	PMID:26246518	PCS		2/4			P	HPO:probinson[2023-03-08]
OMIM:616682	Seizures, scoliosis, and macrocephaly/microcephaly syndrome		HP:0004349	PMID:26246518	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002069	PMID:33658631	PCS		1/12			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000286	PMID:33658631	PCS		2/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002188	PMID:33658631	PCS		1/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000046	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001332	PMID:33658631	PCS		1/13			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001252	PMID:33658631	PCS		5/27			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0003196	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0003593	PMID:33658631	PCS					C	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0032794	PMID:33658631	PCS		1/12			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000639	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000718	PMID:33658631	PCS		3/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000712	PMID:33658631	PCS		1/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0100807	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000637	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002019	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001249	PMID:33658631	PCS		12/12			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001601	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000358	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000252	PMID:33658631	PCS		4/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0007429	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001382	PMID:33658631	PCS		2/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002591	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0011327	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000609	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:4000079	PMID:33658631	PCS		2/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000729	PMID:33658631	PCS		5/12			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001537	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000964	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002901	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001852	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000006	PMID:33658631	PCS					I	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000248	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000126	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000324	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0030799	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000582	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000343	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002121	PMID:33658631	PCS		1/12			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0005274	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001270	PMID:33658631	PCS		11/13			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0012725	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:4000070	PMID:33658631	PCS		1/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001629	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0007021	PMID:33658631	PCS		2/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000739	PMID:33658631	PCS		3/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000733	PMID:33658631	PCS		1/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002837	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0012170	PMID:33658631	PCS		1/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000219	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0006532	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000218	PMID:33658631	PCS		3/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000455	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001863	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000411	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000256	PMID:33658631	PCS		3/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001347	PMID:33658631	PCS		1/13			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0001320	PMID:33658631	PCS		1/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000275	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002136	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000750	PMID:33658631	PCS		14/14			P	HPO:probinson[2023-07-11];HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000431	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002373	PMID:33658631	PCS		1/12			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002099	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000193	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000272	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000470	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0045025	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0012167	PMID:33658631	PCS		2/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000506	PMID:33658631	PCS		2/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0100716	PMID:33658631	PCS		1/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000268	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0002007	PMID:33658631	PCS		2/14			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0007018	PMID:33658631	PCS		4/11			P	HPO:probinson[2023-07-11]
OMIM:620330	Intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities		HP:0000303	PMID:33658631	PCS		1/14			P	HPO:probinson[2023-07-11]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0003236	PMID:8968749	PCS		6/6			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-10-11]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0003621	PMID:8968749	PCS		7/7			C	HPO:probinson[2009-02-17];HPO:probinson[2022-10-11]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0003707	PMID:8968749	PCS		2/7			P	HPO:skoehler[2012-07-20];HPO:probinson[2022-10-11]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0003691	OMIM:604286	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0003560	OMIM:604286	TAS					P	HPO:skoehler[2015-01-21]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0000007	PMID:7581448	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-10-11]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0007126	OMIM:604286	TAS					P	HPO:skoehler[2010-06-20]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0002505	PMID:8968749	PCS	HP:0003621	7/7			P	HPO:probinson[2022-10-11]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0003724	OMIM:604286	TAS					P	HPO:probinson[2009-02-17]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0003325	OMIM:604286	TAS					P	HPO:probinson[2009-02-17]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0001644	OMIM:604286	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:604286	Muscular dystrophy, limb-girdle, type 2E		HP:0008988	OMIM:604286	TAS					P	HPO:probinson[2009-02-17]
OMIM:238950	Hyperopia, high		HP:0008499	OMIM:238950	TAS					P	HPO:skoehler[2009-02-17]
OMIM:238950	Hyperopia, high		HP:0000007	OMIM:238950	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:615360	Leber congenital amaurosis 17		HP:0032284	PMID:23307924	TAS		1/1			P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:615360	Leber congenital amaurosis 17		HP:0000007	PMID:23307924	PCS					I	HPO:skoehler[2014-01-28];HP:probinson[2019-03-02]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0000486	OMIM:240800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0001250	OMIM:240800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0001251	OMIM:240800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0000825	PMID:15356046	PCS		1/1			P	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-17]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0000737	OMIM:240800	TAS					P	HPO:skoehler[2013-11-18]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0001943	PMID:15356046	PCS	HP:0003623	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0002329	OMIM:240800	IEA					P	HPO:iea[2009-02-17]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0001257	OMIM:240800	IEA					P	HPO:iea[2009-02-17]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0000006	PMID:15356046	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2023-02-17]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0001249	OMIM:240800	IEA					P	HPO:iea[2009-02-17]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0001259	OMIM:240800	IEA					P	HPO:iea[2009-02-17]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0001347	OMIM:240800	TAS					P	HPO:skoehler[2013-11-18]
OMIM:240800	Hypoglycemia of infancy, leucine-sensitive		HP:0003623	PMID:15356046	PCS		1/1			C	HPO:probinson[2023-02-17]
OMIM:237450	Hyperbilirubinemia, Rotor type, digenic		HP:0001000	OMIM:237450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:237450	Hyperbilirubinemia, Rotor type, digenic		HP:0002908	OMIM:237450	IEA					P	HPO:iea[2009-02-17]
OMIM:237450	Hyperbilirubinemia, Rotor type, digenic		HP:0000924	OMIM:237450	IEA					P	HPO:iea[2009-02-17]
OMIM:237450	Hyperbilirubinemia, Rotor type, digenic		HP:0010984	PMID:22232210	PCS					I	HPO:probinson[2020-07-23]
OMIM:237450	Hyperbilirubinemia, Rotor type, digenic		HP:0000952	OMIM:237450	IEA					P	HPO:iea[2009-02-17]
OMIM:613711	Hirschsprung disease, susceptibility to, 3		HP:0003577	PMID:8968758	PCS		2/2			C	HPO:probinson[2023-01-16]
OMIM:613711	Hirschsprung disease, susceptibility to, 3		HP:0011286	PMID:8968758	PCS		1/2			P	HPO:probinson[2023-01-16]
OMIM:613711	Hirschsprung disease, susceptibility to, 3		HP:0002251	PMID:8896568	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-16]
OMIM:613711	Hirschsprung disease, susceptibility to, 3		HP:0011285	PMID:8968758	PCS		1/2			P	HPO:probinson[2023-01-16]
OMIM:613711	Hirschsprung disease, susceptibility to, 3		HP:0000006	PMID:8968758	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-16]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0010804	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000189	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0008070	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0008873	PMID:31564437	PCS					P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000414	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000218	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000774	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0002953	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000278	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000358	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0009901	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0002553	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0002751	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000252	PMID:31564437	PCS		3/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000750	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000592	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0001263	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0011800	PMID:31564437	PCS					P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0002194	PMID:31564437	PCS		5/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000007	PMID:31564437	PCS					I	HPO:probinson[2020-07-20];HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000307	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0001511	PMID:31564437	PCS					P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0001357	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0001555	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0002645	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000248	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000303	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0000369	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0005855	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0005338	PMID:31564437	PCS		1/5			P	HPO:probinson[2020-07-20]
OMIM:618644	Osteogenesis imperfecta, type XX		HP:0006349	PMID:31564437	PCS		2/5			P	HPO:probinson[2020-07-20]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0002257	PMID:25927852	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0031417	PMID:25927852	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0000365	PMID:25927852	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0001696	PMID:25927852	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0001651	PMID:25927852	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0002110	PMID:25927852	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0030828	PMID:25927852	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0011463	PMID:25927852	PCS		1/1			C	HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0012020	PMID:25927852	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0008222	PMID:25927852	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0000007	PMID:25927852	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0000821	PMID:25927852	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617577	Ciliary dyskinesia, primary, 37		HP:0000853	PMID:25927852	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:616669	Immunodeficiency 45		HP:0020088	PMID:26424569	PCS	HP:0003593	1/1			P	HPO:probinson[2019-04-20]
OMIM:616669	Immunodeficiency 45		HP:0000007	OMIM:616669	TAS					I	HPO:skoehler[2017-07-13]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0001265	OMIM:613077	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0002015	PMID:21646632	PCS		4/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0000365	OMIM:613077	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0003750	OMIM:613077	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0003596	PMID:21646632	PCS		4/7			C	HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0003198	OMIM:613077	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0000590	PMID:21646632	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0001260	OMIM:613077	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0002066	OMIM:613077	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0001251	PMID:21646632	PCS		2/7			P	HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0012378	PMID:21646632	PCS		5/7			P	HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0000716	OMIM:613077	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0001618	PMID:21646632	PCS		1/7			P	HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0011462	PMID:21646632	PCS		3/7			C	HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0000739	OMIM:613077	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0000508	PMID:21646632	PCS		6/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0000006	PMID:19664747	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0000501	PMID:21646632	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-29]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0003546	OMIM:613077	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613077	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5		HP:0003689	PMID:21646632	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-29]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0007989	OMIM:305390	PCS					P	HPO:probinson[2018-03-07]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0000594	PMID:17325173	PCS		1/4			P	HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0030666	PMID:17325173	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0000541	PMID:17325173	PCS		3/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0000490	OMIM:305390	TAS					P	HPO:probinson[2015-12-22]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0001493	PMID:20159112	PCS					P	HPO:probinson[2018-03-07]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0003593	PMID:17325173	PCS		1/4			C	HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0011532	PMID:8457509	PCS					P	HPO:probinson[2018-03-07]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0011003	PMID:17325173	PCS		1/4			P	HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0012841	PMID:17325173	PCS		1/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0008052	PMID:17325173	PCS		1/4			P	HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0000639	OMIM:305390	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0011530	OMIM:305390	TAS		HP:0040283			P	HPO:skoehler[2015-10-09]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0001419	PMID:20159112	PCS					I	HPO:probinson[2018-03-07]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0011463	PMID:17325173	PCS		3/4			C	HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0000568	OMIM:305390	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0007685	PMID:17325173	PCS		3/4			P	HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0007663	PMID:17325173	PCS		4/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-05-06]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0030490	OMIM:305390	TAS					P	HPO:probinson[2018-03-07]
OMIM:305390	Exudative vitreoretinopathy 2, X-linked		HP:0007710	PMID:1642288	PCS					P	HPO:probinson[2018-03-07]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0000252	PMID:23603762	PCS		2/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0002510	PMID:23603762	PCS		2/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0032409	PMID:23603762	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0007074	PMID:23603762	PCS		2/3			P	HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0000518	PMID:23603762	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0001250	PMID:23603762	PCS		2/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0001263	PMID:23603762	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0031882	PMID:23603762	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0001302	PMID:23603762	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0000006	PMID:23603762	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0033725	PMID:23603762	PCS		1/3			P	HPO:probinson[2022-09-08]
OMIM:615412	Cortical dysplasia, complex, with other brain malformations 4		HP:0012469	PMID:23603762	PCS		1/3			P	HPO:probinson[2022-09-08]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0000252	PMID:33513338	PCS		7/31			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0000750	PMID:33513338	PCS		32/36			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0002353	PMID:33513338	PCS		19/24			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0002376	PMID:33513338	PCS		6/35			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001250	PMID:33513338	PCS		22/36			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001260	PMID:33513338	PCS		6/20			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001263	PMID:33513338	PCS		35/36			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001252	PMID:33513338	PCS		28/37			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001251	PMID:33513338	PCS		6/27			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001270	PMID:33513338	PCS		34/37			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0000708	PMID:33513338	PCS		24/34			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001257	PMID:33513338	PCS		10/36			P	HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0000006	PMID:33513338	PCS					I	HPO:probinson[2021-05-14];HPO:probinson[2021-05-14]
OMIM:619228	Developmental delay with dysmorphic facies and dental anomalies		HP:0001249	PMID:33513338	PCS		28/31			P	HPO:probinson[2021-05-14]
OMIM:607016	Scheie syndrome		HP:0001650	PMID:10220555	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-13]
OMIM:607016	Scheie syndrome		HP:0007957	PMID:10220555	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-13]
OMIM:607016	Scheie syndrome		HP:0003302	OMIM:607016	IEA					P	HPO:skoehler[2019-09-07]
OMIM:607016	Scheie syndrome		HP:0002870	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0001761	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0000293	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0002341	OMIM:607016	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607016	Scheie syndrome		HP:0000283	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0000470	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0005280	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0012185	OMIM:607016	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607016	Scheie syndrome		HP:0001718	PMID:10220555	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607016	Scheie syndrome		HP:0000943	OMIM:607016	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:607016	Scheie syndrome		HP:0000007	PMID:10220555	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-13]
OMIM:607016	Scheie syndrome		HP:0000546	OMIM:607016	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0001659	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0002857	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0000501	OMIM:607016	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0001249	PMID:7550232;PMID:10220555	PCS		0/3			P	HPO:probinson[2024-03-13];HPO:skoehler[2014-11-26];HPO:probinson[2024-03-13]
OMIM:607016	Scheie syndrome		HP:0000303	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607016	Scheie syndrome		HP:0000445	OMIM:607016	TAS					P	HPO:skoehler[2014-01-28]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0031834	PMID:27616478	PCS		1/3			P	HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0003577	PMID:27616478	PCS		3/3			C	HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0011539	PMID:27616478	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0001651	PMID:27616478	PCS		1/2			P	HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0003363	PMID:27616478	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0004383	PMID:27616478	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0011538	PMID:27616478	PCS		1/3			P	HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0011579	PMID:27616478	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0001629	PMID:27616478	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-23];HPO:probinson[2025-05-03]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0011540	PMID:27616478	PCS		1/3			P	HPO:probinson[2025-05-03]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0001719	PMID:27616478	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0012020	PMID:27616478	PCS		1/3			P	HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0000007	PMID:27616478	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-23]
OMIM:617205	Heterotaxy, visceral, 8, autosomal		HP:0004935	PMID:27616478	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0003577	PMID:26518474	PCS		1/1			C	HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0002540	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0000023	PMID:26518474	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0001162	PMID:26518474	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0001252	PMID:26518474	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0001263	PMID:26518474	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0001251	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0012745	PMID:26518474	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0002282	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0001270	PMID:26518474	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0011802	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0005280	PMID:26518474	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0000508	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0000657	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0002419	OMIM:617563	IEA		0/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0000007	PMID:26518474	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0002119	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0000488	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0001830	PMID:26518474	PCS		1/1			P	HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0000278	PMID:26518474	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0000369	PMID:26518474	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-23]
OMIM:617563	Orofaciodigital syndrome XVI		HP:0002104	OMIM:617563	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0000253	PMID:16033914	PCS		1/10			P	HPO:probinson[2021-06-01]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0000750	PMID:16033914	PCS		10/10			P	HPO:probinson[2021-06-01]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0011463	PMID:14569116	PCS		10/10			C	HPO:probinson[2022-06-16]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0001263	PMID:16033914	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-01]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0000338	PMID:14569116	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-16]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0000007	PMID:16033914	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-01]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0000736	PMID:14569116	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-16]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0000752	PMID:14569116	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-16]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0002546	PMID:14569116	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-16]
OMIM:608443	Intellectual developmental disorder, autosomal recessive 3		HP:0010864	PMID:16033914;PMID:14569116	PCS		20/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-01];HPO:probinson[2022-06-16]
OMIM:615374	Cone-Rod dystrophy 18		HP:0003621	PMID:23746546	PCS		3/4			C	HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0025010	PMID:23746546	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0011463	PMID:23746546	PCS		1/4			C	HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0008001	PMID:23746546	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0000007	PMID:23746546	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0007663	PMID:23746546	PCS		4/4			P	HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0000603	PMID:23746546	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0011003	PMID:23746546	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-29]
OMIM:615374	Cone-Rod dystrophy 18		HP:0000548	PMID:23746546	PCS		5/5			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-03-29]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0001199	OMIM:124480	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0001770	OMIM:124480	TAS					P	HPO:skoehler[2009-02-17]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0001792	PMID:28396750	PCS		1/1			P	HPO:probinson[2012-03-03];HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0003577	PMID:24913193	PCS		3/3			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0007529	OMIM:124480	IEA					P	HPO:skoehler[2009-02-17]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0008619	PMID:28396750	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0001156	OMIM:124480	TAS					P	HPO:skoehler[2014-11-26]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0001592	OMIM:124480	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0200104	PMID:24913193	PCS		3/3			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0012554	PMID:28396750	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0009162	PMID:24913193	PCS		3/3			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0000407	PMID:24913193	PCS		3/3			P	HPO:probinson[2013-12-16];HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0000348	PMID:28396750	IEA		1/1			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0005707	PMID:28396750	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0001802	PMID:28396750	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0008404	PMID:24913193	PCS		3/3			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0000006	PMID:24913193	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0001249	PMID:24913193	PCS		0/3			P	HPO:probinson[2022-03-04]
OMIM:124480	Deafness, congenital, and onychodystrophy, autosomal dominant		HP:0000698	OMIM:124480	TAS		HP:0040283			P	HPO:probinson[2015-02-02]
OMIM:613705	Orofacial cleft 10		HP:0003577	PMID:16990542	PCS		1/1			C	HPO:probinson[2022-11-01]
OMIM:613705	Orofacial cleft 10		HP:0100334	PMID:16990542	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2022-11-01]
OMIM:613705	Orofacial cleft 10		HP:0003745	PMID:16990542	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-01]
OMIM:613705	Orofacial cleft 10		HP:0100333	PMID:16990542	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2022-11-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002168	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0003596	PMID:16717236	PCS		1/2			C	HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002067	PMID:16717236	PCS		1/2			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0001310	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0001250	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0001272	PMID:16717236	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0001271	PMID:16717236	PCS		2/2			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002066	PMID:16717236	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0000020	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002062	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0000639	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0000716	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0011462	PMID:16717236	IEA		1/2			C	HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0003829	OMIM:603516	IEA					I	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0007289	PMID:16717236	PCS		1/2			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002936	PMID:16717236	PCS		1/2			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0003743	OMIM:603516	IEA					I	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0001347	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002311	OMIM:603516	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002015	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0000012	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0003487	PMID:16717236	PCS		1/2			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0001260	PMID:16717236	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002075	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002073	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002070	PMID:16717236	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0002071	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0000726	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0007772	PMID:16717236	PCS		1/2			P	HPO:probinson[2022-07-01];HPO:probinson[2022-07-01]
OMIM:603516	Spinocerebellar ataxia 10		HP:0007256	OMIM:603516	TAS					P	HPO:skoehler[2015-01-04]
OMIM:603516	Spinocerebellar ataxia 10		HP:0000762	OMIM:603516	IEA					P	HPO:iea[2009-02-17]
OMIM:603516	Spinocerebellar ataxia 10		HP:0000006	PMID:11017075	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:101600	Pfeiffer syndrome		HP:0000244	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0000486	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0003795	OMIM:101600	TAS					P	HPO:probinson[2012-06-09]
OMIM:101600	Pfeiffer syndrome		HP:0002780	OMIM:101600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:101600	Pfeiffer syndrome		HP:0003196	OMIM:101600	TAS					P	HPO:probinson[2012-04-24]
OMIM:101600	Pfeiffer syndrome		HP:0004440	OMIM:101600	TAS					P	HPO:probinson[2012-04-24]
OMIM:101600	Pfeiffer syndrome		HP:0003070	OMIM:101600	IEA					P	HPO:skoehler[2012-10-09]
OMIM:101600	Pfeiffer syndrome		HP:0010055	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0006110	OMIM:101600	TAS					P	HPO:probinson[2012-06-09]
OMIM:101600	Pfeiffer syndrome		HP:0000316	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0000238	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0000678	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0000218	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0001249	OMIM:101600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:101600	Pfeiffer syndrome		HP:0002676	OMIM:101600	IEA		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:101600	Pfeiffer syndrome		HP:0000494	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0005347	OMIM:101600;PMID:15996217	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-19]
OMIM:101600	Pfeiffer syndrome		HP:0000453	OMIM:101600	TAS					P	HPO:probinson[2012-04-24]
OMIM:101600	Pfeiffer syndrome		HP:0000452	OMIM:101600	TAS					P	HPO:probinson[2012-04-24]
OMIM:101600	Pfeiffer syndrome		HP:0003041	OMIM:101600	TAS					P	HPO:probinson[2012-04-24]
OMIM:101600	Pfeiffer syndrome		HP:0005280	OMIM:101600	TAS					P	HPO:probinson[2012-04-24]
OMIM:101600	Pfeiffer syndrome		HP:0011304	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:6000648	PMID:25251565	PCS		1/5			P	HPO:probinson[2024-04-03]
OMIM:101600	Pfeiffer syndrome		HP:0000327	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0002308	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0006101	OMIM:101600	TAS					P	HPO:skoehler[2014-06-24]
OMIM:101600	Pfeiffer syndrome		HP:0001159	OMIM:101600	TAS					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0000586	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0000006	OMIM:101600	IEA					I	HPO:iea[2009-02-17]
OMIM:101600	Pfeiffer syndrome		HP:0000303	OMIM:101600	IEA					P	HPO:iea[2009-02-17]
OMIM:185500	Supravalvular aortic stenosis		HP:0004950	OMIM:185500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:185500	Supravalvular aortic stenosis		HP:0004381	OMIM:185500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:185500	Supravalvular aortic stenosis		HP:0001642	OMIM:185500	TAS					P	HPO:probinson[2013-12-20]
OMIM:185500	Supravalvular aortic stenosis		HP:0000006	OMIM:185500	TAS					I	HPO:skoehler[2009-02-17]
OMIM:185500	Supravalvular aortic stenosis		HP:0004415	OMIM:185500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0001771	PMID:33861953	PCS		11/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003676	PMID:33861953	PCS		22/23			C	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003236	PMID:33861953	PCS		10/22			P	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003593	PMID:33861953	PCS		4/12			C	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0030319	PMID:33861953	PCS		4/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0011463	PMID:33861953	PCS		3/12			C	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0011462	PMID:33861953	PCS		3/12			C	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0032341	PMID:33861953	PCS		13/20			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003306	PMID:33861953	PCS		7/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003202	PMID:33861953	PCS		8/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003621	PMID:33861953	PCS		2/12			C	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0002650	PMID:33861953	PCS		12/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0000750	PMID:33861953	PCS		3/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0008959	PMID:33861953	PCS		15/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003044	PMID:33861953	PCS		3/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003560	PMID:33861953	PCS		12/14			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0006380	PMID:33861953	PCS		4/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0009053	PMID:33861953	PCS		18/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0001716	PMID:33861953	PCS		1/23			P	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0000729	PMID:33861953	PCS		1/23			P	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0000508	PMID:33861953	PCS		4/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0000007	PMID:33861953	PCS					I	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0001638	PMID:33861953	PCS		2/23			P	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0002505	PMID:33861953	PCS		8/23			P	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003712	PMID:33861953	PCS		6/23			P	HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0002987	PMID:33861953	PCS		6/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0000467	PMID:33861953	PCS		19/23			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003458	PMID:33861953	PCS		16/19			P	HPO:probinson[2021-11-21];HPO:probinson[2021-11-21]
OMIM:619566	Muscular dystrophy, limb-girdle, autosomal recessive 27		HP:0003557	PMID:33861953	PCS		2/14			P	HPO:probinson[2021-11-21]
OMIM:612433	Deafness, autosomal recessive 45		HP:0001751	PMID:18325041	PCS		0/4			P	HP:probinson[2019-03-09];HPO:probinson[2024-03-14]
OMIM:612433	Deafness, autosomal recessive 45		HP:0000007	PMID:18325041	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-09]
OMIM:612433	Deafness, autosomal recessive 45		HP:0000399	PMID:18325041	PCS		4/4			P	HP:probinson[2019-03-09]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001410	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003355	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001250	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001252	PMID:10636738	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000580	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003593	PMID:10636738	PCS		2/2			C	HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002240	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003076	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001251	PMID:10636738	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001290	PMID:9843204	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001270	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0030319	OMIM:220110	IEA					P	HPO:skoehler[2019-09-07]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001508	PMID:10636738	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001903	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001427	OMIM:220110	TAS					I	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002878	PMID:10636738	PCS		2/2			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003109	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000218	OMIM:220110	IEA					P	HPO:skoehler[2019-09-07]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000597	PMID:10636738	PCS		2/2			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001249	OMIM:220110	IEA					P	HPO:skoehler[2010-06-18]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003688	PMID:9843204;PMID:10636738	PCS		15/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001348	PMID:9843204	PCS		11/11			P	HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003128	PMID:9843204;PMID:10636738	PCS		13/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03];HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002875	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003546	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002078	PMID:9843204	PCS		11/11			P	HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002376	PMID:9843204;PMID:10636738	PCS		13/13			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002098	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002352	OMIM:220110	IEA					P	HPO:skoehler[2018-10-08]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002151	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001263	OMIM:220110	TAS					P	HPO:skoehler[2014-04-04]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002490	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000093	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0003819	PMID:10636738	PCS		2/2			C	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000407	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001639	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0012240	OMIM:220110	TAS					P	HPO:probinson[2013-04-01]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000508	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000007	PMID:9843204	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000648	PMID:10636738	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0002747	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0006565	OMIM:220110	TAS					P	HPO:probinson[2012-07-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0000124	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:220110	Mitochondrial complex IV deficiency, nuclear type 1		HP:0001994	OMIM:220110	IEA					P	HPO:iea[2009-02-17]
OMIM:614042	Moyamoya disease 5		HP:0004970	OMIM:614042	TAS					P	HPO:probinson[2013-08-10]
OMIM:614042	Moyamoya disease 5		HP:0011834	PMID:19409525	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-22]
OMIM:614042	Moyamoya disease 5		HP:0000006	PMID:19409525	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-22]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0003202	OMIM:105300	IEA					P	HPO:iea[2009-02-17]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0001332	OMIM:105300	IEA					P	HPO:iea[2009-02-17]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0000639	OMIM:105300	IEA					P	HPO:iea[2009-02-17]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0000020	OMIM:105300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0002607	OMIM:105300	IEA					P	HPO:iea[2009-02-17]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0001258	OMIM:105300	IEA					P	HPO:iea[2009-02-17]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0000006	OMIM:105300	IEA					I	HPO:iea[2009-02-17]
OMIM:105300	Amyotrophic dystonic paraplegia		HP:0001249	OMIM:105300	IEA					P	HPO:iea[2009-02-17]
OMIM:604537	Leber congenital amaurosis 5		HP:0000550	PMID:17546029	PCS					P	HPO:skoehler[2013-02-23]
OMIM:604537	Leber congenital amaurosis 5		HP:0000572	OMIM:604537	IEA	HP:0003577				P	HPO:skoehler[2019-09-07]
OMIM:604537	Leber congenital amaurosis 5		HP:0000540	PMID:17546029	PCS					P	HPO:skoehler[2013-02-23]
OMIM:604537	Leber congenital amaurosis 5		HP:0000639	PMID:17546029	PCS					P	HPO:skoehler[2013-02-23]
OMIM:604537	Leber congenital amaurosis 5		HP:0003593	OMIM:604537	IEA					C	HPO:skoehler[2019-09-07]
OMIM:604537	Leber congenital amaurosis 5		HP:0008499	OMIM:604537	IEA					P	HPO:skoehler[2019-09-07]
OMIM:604537	Leber congenital amaurosis 5		HP:0000007	PMID:17546029	PCS					I	HPO:skoehler[2013-01-09]
OMIM:604537	Leber congenital amaurosis 5		HP:0000505	PMID:17546029	PCS	HP:0003577				P	HPO:skoehler[2013-02-23]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002202	PMID:29299831	PCS		HP:0040284			P	HPO:probinson[2020-08-26];HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002240	OMIM:181000	PCS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001094	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0010702	OMIM:181000	PCS					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0012424	OMIM:181000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0032976	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0100721	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0000613	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0006530	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0100749	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001945	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001824	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0003745	OMIM:181000	TAS					I	HPO:skoehler[2015-12-30]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0000554	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001744	OMIM:181000	PCS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002039	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001369	OMIM:181000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0003565	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0009926	OMIM:181000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002113	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002037	OMIM:181000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002110	PMID:10430755	PCS		HP:0040283			P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0003581	PMID:10430755	PCS					C	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002097	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002094	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0012735	OMIM:181000	TAS					P	HPO:skoehler[2014-03-24]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002150	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002092	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0012418	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0011840	OMIM:181000	TAS					P	HPO:skoehler[2018-10-08]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002091	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0012062	OMIM:181000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0010286	OMIM:181000	TAS					P	HP:probinson[2018-07-04]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001217	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0008940	OMIM:181000	TAS					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001698	PMID:29299831	PCS		HP:0040284			P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002206	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0000006	OMIM:181000	IEA					I	HPO:skoehler[2019-04-18]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0000622	OMIM:181000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0007734	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0000501	OMIM:181000	IEA					P	HPO:probinson[2009-02-17]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001876	OMIM:181000	TAS					P	HPO:skoehler[2013-01-22]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0002105	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:181000	Sarcoidosis, susceptibility to, 1		HP:0001138	OMIM:181000	PCS		HP:0040283			P	HPO:probinson[2012-04-06]
OMIM:600989	Infundibulopelvic dysgenesis		HP:0002907	OMIM:600989	IEA					P	HPO:iea[2009-02-17]
OMIM:600989	Infundibulopelvic dysgenesis		HP:0000003	OMIM:600989	IEA					P	HPO:iea[2009-02-17]
OMIM:600989	Infundibulopelvic dysgenesis		HP:0000006	OMIM:600989	IEA					I	HPO:iea[2009-02-17]
OMIM:600989	Infundibulopelvic dysgenesis		HP:0002027	OMIM:600989	IEA					P	HPO:iea[2009-02-17]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0030502	PMID:30635494	PCS		2/4			P	HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003621	PMID:30635494	PCS		1/4			C	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0010628	OMIM:610542	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003200	PMID:30635494	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003388	OMIM:610542	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003473	OMIM:610542	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003394	OMIM:610542	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0001270	PMID:30635494	PCS		4/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003391	OMIM:610542	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0008180	OMIM:610542	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0011463	PMID:30635494	PCS		1/4			C	HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0000508	OMIM:610542	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0000007	PMID:21310273	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0002515	PMID:30635494	PCS		2/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0007126	OMIM:610542	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003701	PMID:30635494	PCS		4/4			P	HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0000597	OMIM:610542	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003623	PMID:30635494	PCS		2/4			C	HPO:probinson[2023-06-10]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0000467	OMIM:610542	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610542	Myasthenic syndrome, congenital, with tubular aggregates 1		HP:0003403	PMID:30635494	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-06-10]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0030953	PMID:29366613	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0009926	OMIM:148200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0003621	PMID:29366613	PCS		29/33			C	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0007759	PMID:29366613	PCS		18/34			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0000491	PMID:29366613	PCS		34/34			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0011462	PMID:29366613	PCS		4/33			C	HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0000613	PMID:29366613	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0100014	PMID:29366613	PCS		2/34			P	HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0000006	PMID:29366613	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-26]
OMIM:148200	Keratoendotheliitis fugax hereditaria		HP:0000622	PMID:29366613	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0003577	PMID:28559357	PCS		2/5			C	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0001915	PMID:24085763	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0001903	PMID:24085763	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0011463	PMID:28559357	PCS		2/5			C	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0003593	PMID:28559357	PCS		1/5			C	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0006254	PMID:24085763	PCS		0/1			P	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0000007	PMID:24085763	PCS					I	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0005528	PMID:24085763;PMID:28559357	PCS		6/6			P	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0001873	PMID:24085763;PMID:28559357	PCS		7/7			P	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0001876	PMID:28559357	PCS		5/5			P	HPO:probinson[2024-02-11]
OMIM:620481	Amegakaryocytic thrombocytopenia, congenital, 2		HP:0001875	PMID:24085763	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003510	PMID:11279527	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002983	PMID:11279527	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003577	PMID:11279527	PCS		2/2			C	HPO:probinson[2023-02-21];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002089	PMID:11279527	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0005257	PMID:11279527	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001195	PMID:11279527	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000160	PMID:11279527	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002085	PMID:11279527	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0012368	PMID:11279527	PCS		1/2			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000518	PMID:11279527	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001548	OMIM:224410	IEA					P	HPO:skoehler[2010-06-20]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0008873	PMID:11279527	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002879	PMID:11279527	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000358	PMID:11279527	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003026	PMID:11279527	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000252	PMID:11279527	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000431	PMID:11279527	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001762	PMID:11279527	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001362	PMID:11279527	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000272	OMIM:224410	IEA					P	HPO:iea[2009-02-17]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002093	PMID:11279527	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000007	PMID:11279527	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0006487	OMIM:224410	TAS					P	HPO:probinson[2012-06-03]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003811	PMID:11279527	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001059	PMID:11279527	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000347	PMID:11279527	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:224410	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000028	PMID:11279527	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0002257	PMID:22102620	PCS		2/2			P	HPO:probinson[2022-02-24]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0001696	PMID:18022865;PMID:12142464	PCS		2/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-25];HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0001651	PMID:12142464	PCS		1/1			P	HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0002110	PMID:18022865	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0033036	PMID:22102620	PCS		2/2			P	HPO:probinson[2022-02-24]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0012735	PMID:22102620	PCS		2/2			P	HPO:probinson[2022-02-24]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0012258	PMID:12142464	PCS		0/1			P	HPO:probinson[2013-04-07];HPO:probinson[2021-02-25];HPO:probinson[2024-03-14]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0002091	PMID:18022865	PCS		2/4			P	HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0030877	PMID:18022865	PCS		2/4			P	HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0012265	PMID:22102620;PMID:12142464	PCS		3/3			P	HPO:probinson[2022-02-24];HPO:skoehler[2015-01-19];HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0011463	PMID:22102620	PCS		2/2			C	HPO:probinson[2022-02-24]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0012262	PMID:18022865	PCS		4/4			P	HPO:probinson[2013-04-07];HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0000007	PMID:12142464	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-02-25]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0000403	PMID:22102620	PCS		2/2			P	HPO:probinson[2022-02-24]
OMIM:611884	Ciliary dyskinesia, primary, 7		HP:0006532	PMID:18022865	PCS		5/6			P	HPO:probinson[2021-02-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0003577	PMID:15981765	PCS		2/2			C	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0000486	PMID:26197978	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001310	PMID:26197978;PMID:27016154;PMID:15981765	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001332	PMID:26197978	PCS		1/1			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001272	PMID:27016154	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002066	PMID:27016154	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001252	PMID:26197978;PMID:25361784	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001251	PMID:27016154	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0003593	PMID:27016154	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0012389	PMID:15981765	PCS	HP:0003621	2/2			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002080	PMID:26197978;PMID:27016154	PCS		2/2			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0011463	PMID:26197978	PCS		1/1			C	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0000657	PMID:26197978	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002317	PMID:27016154;PMID:15981765	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002359	PMID:15981765	PCS		2/2			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001249	PMID:25361784	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001347	PMID:15981765	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001320	PMID:26197978;PMID:25361784	PCS		3/3			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002136	PMID:26197978	PCS		1/1			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002312	PMID:26197978	PCS		1/1			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0000750	PMID:27016154	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0000574	PMID:27016154	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002078	PMID:25361784	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001321	PMID:26197978;PMID:25361784	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0003388	PMID:26197978	PCS		1/1			P	HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001260	PMID:26197978;PMID:27016154;PMID:15981765	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0001263	PMID:25361784	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0002070	PMID:25361784	PCS		2/2			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0040196	PMID:27016154	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0000007	PMID:25361784	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0000664	PMID:27016154	PCS		1/1			P	HPO:probinson[2022-09-25]
OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		HP:0003677	PMID:27016154	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0004401	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0001288	PMID:27590285	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0003388	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0011968	PMID:27590285	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0001252	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0003593	PMID:27590285	PCS		2/2			C	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0002093	PMID:27590285	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0012378	PMID:27590285	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0030319	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0006380	PMID:27590285	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0000508	PMID:27590285	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0030197	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0030890	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0000602	PMID:27590285	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0000007	PMID:27590285	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0000961	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0002104	PMID:27590285	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0000666	PMID:27590285	PCS		1/2			P	HPO:probinson[2023-05-08]
OMIM:617239	Myasthenic syndrome, congenital, 21, presynaptic		HP:0003546	PMID:27590285	PCS		2/2			P	HPO:skoehler[2017-07-13]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002300	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0003477	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0006802	OMIM:611890	IEA					P	HPO:skoehler[2015-01-19]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0003577	OMIM:611890	IEA					C	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002540	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001332	OMIM:611890	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001250	OMIM:611890	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001290	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001270	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0011220	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0003828	OMIM:611890	IEA					M	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000954	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001349	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002878	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001989	OMIM:611890	TAS					P	HPO:probinson[2013-04-03]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000218	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000278	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001348	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0003202	OMIM:611890	TAS				HP:0012828	P	HPO:probinson[2013-04-03]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002058	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001188	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000494	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000252	OMIM:611890	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002059	OMIM:611890	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001385	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001762	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002650	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001288	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0011968	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001260	OMIM:611890	IEA					P	HPO:skoehler[2019-09-07]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000470	OMIM:611890	TAS					P	HPO:probinson[2013-04-03]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0001838	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002808	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000508	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0007277	OMIM:611890	TAS					P	HPO:probinson[2013-04-03]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000007	OMIM:611890	TAS					I	HPO:probinson[2013-01-09]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002804	OMIM:611890	TAS					P	HPO:probinson[2013-04-03]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002747	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0003811	OMIM:611890	TAS					C	HPO:probinson[2013-04-03]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000369	OMIM:611890	TAS					P	HPO:probinson[2013-04-03]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000028	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000545	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0000347	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:611890	Congenital arthrogryposis with anterior horn cell disease		HP:0002522	OMIM:611890	IEA					P	HPO:skoehler[2019-04-18]
OMIM:236000	Lymphoma, hodgkin		HP:0012189	PMID:19706467	PCS		3/7			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-05-14]
OMIM:236000	Lymphoma, hodgkin		HP:0000007	OMIM:236000	IEA					I	HPO:iea[2009-02-17]
OMIM:236000	Lymphoma, hodgkin		HP:0003459	OMIM:236000	IEA					P	HPO:iea[2009-02-17]
OMIM:236000	Lymphoma, hodgkin		HP:0003347	OMIM:236000	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0003577	PMID:29891882	PCS		1/1			C	HPO:probinson[2023-03-26]
OMIM:602152	Rhyns syndrome		HP:0002684	PMID:29891882	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:602152	Rhyns syndrome		HP:0004322	OMIM:602152	IEA					P	HPO:skoehler[2019-04-18]
OMIM:602152	Rhyns syndrome		HP:0001156	OMIM:602152	IEA					P	HPO:skoehler[2019-02-22]
OMIM:602152	Rhyns syndrome		HP:0000083	OMIM:602152	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0012622	OMIM:602152	IEA					P	HPO:skoehler[2019-02-22]
OMIM:602152	Rhyns syndrome		HP:0100864	PMID:29891882	PCS		1/1			P	HPO:skoehler[2019-02-22]
OMIM:602152	Rhyns syndrome		HP:0000939	PMID:29891882	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:602152	Rhyns syndrome		HP:0000938	PMID:29891882	PCS		1/1			P	HPO:skoehler[2019-02-22]
OMIM:602152	Rhyns syndrome		HP:0000510	PMID:29891882	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0000577	PMID:29891882	PCS		1/1			P	HPO:skoehler[2019-02-22]
OMIM:602152	Rhyns syndrome		HP:0000830	OMIM:602152	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0007824	PMID:29891882	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:602152	Rhyns syndrome		HP:0002652	OMIM:602152	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0003026	PMID:29891882	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:602152	Rhyns syndrome		HP:0002750	PMID:29891882	PCS		1/1			P	HPO:skoehler[2019-02-22]
OMIM:602152	Rhyns syndrome		HP:0000490	OMIM:602152	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0034323	PMID:29891882	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:602152	Rhyns syndrome		HP:0000090	PMID:29891882	PCS		1/1			P	HPO:skoehler[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0000407	PMID:29891882	PCS		1/1			P	HPO:probinson[2023-03-26]
OMIM:602152	Rhyns syndrome		HP:0000508	PMID:29891882	PCS		1/1			P	HPO:skoehler[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0008245	OMIM:602152	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0000007	PMID:29891882	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:602152	Rhyns syndrome		HP:0000824	OMIM:602152	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0000405	OMIM:602152	IEA					P	HPO:iea[2009-02-17]
OMIM:602152	Rhyns syndrome		HP:0002986	PMID:29891882	PCS		1/1			P	HPO:skoehler[2019-02-22]
OMIM:229120	Fountain syndrome		HP:0004279	OMIM:229120	TAS					P	HPO:skoehler[2009-02-17]
OMIM:229120	Fountain syndrome		HP:0002684	OMIM:229120	IEA					P	HPO:iea[2009-02-17]
OMIM:229120	Fountain syndrome		HP:0004322	OMIM:229120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229120	Fountain syndrome		HP:0000282	OMIM:229120	IEA					P	HPO:iea[2009-02-17]
OMIM:229120	Fountain syndrome		HP:0001250	OMIM:229120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229120	Fountain syndrome		HP:0000407	OMIM:229120	IEA					P	HPO:iea[2009-02-17]
OMIM:229120	Fountain syndrome		HP:0000007	OMIM:229120	IEA					I	HPO:iea[2009-02-17]
OMIM:229120	Fountain syndrome		HP:0000280	OMIM:229120	IEA					P	HPO:iea[2009-02-17]
OMIM:229120	Fountain syndrome		HP:0000179	OMIM:229120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229120	Fountain syndrome		HP:0001169	OMIM:229120	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229120	Fountain syndrome		HP:0001249	OMIM:229120	IEA					P	HPO:iea[2009-02-17]
OMIM:229120	Fountain syndrome		HP:0009836	OMIM:229120	IEA					P	HPO:iea[2009-02-17]
OMIM:615348	Nemaline myopathy 8		HP:0002015	PMID:23746549	PCS		23/24			P	HPO:skoehler[2015-08-23];HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0010628	PMID:23746549	PCS		23/23			P	HPO:skoehler[2015-08-23];HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0001561	PMID:23746549	PCS	HP:0030674	14/29			P	HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0001371	PMID:23746549	PCS		24/27			P	HPO:skoehler[2015-08-23];HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0011471	PMID:23746549	PCS	HP:0003593	13/24			P	HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0000007	PMID:23746549	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0001558	PMID:23746549	PCS					P	HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0002878	PMID:23746549	PCS		28/29			P	HPO:skoehler[2015-08-23];HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0001989	PMID:23746549	PCS					P	HPO:skoehler[2015-08-23];HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0003715	PMID:23746549	PCS					P	HPO:skoehler[2015-08-23];HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0001324	PMID:23746549	PCS		29/29			P	HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0001522	PMID:23746549	PCS					C	HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0000597	PMID:23746549	PCS		4/23			P	HPO:probinson[2020-05-10]
OMIM:615348	Nemaline myopathy 8		HP:0003798	PMID:23746549	PCS					P	HPO:skoehler[2015-08-23];HPO:probinson[2020-05-10]
OMIM:208850	Ataxia-Deafness-Retardation syndrome		HP:0000408	OMIM:208850	IEA					P	HPO:iea[2009-02-17]
OMIM:208850	Ataxia-Deafness-Retardation syndrome		HP:0001251	OMIM:208850	IEA					P	HPO:iea[2009-02-17]
OMIM:208850	Ataxia-Deafness-Retardation syndrome		HP:0000007	OMIM:208850	IEA					I	HPO:iea[2009-02-17]
OMIM:208850	Ataxia-Deafness-Retardation syndrome		HP:0001249	OMIM:208850	IEA					P	HPO:iea[2009-02-17]
OMIM:188030	Thrombocytopenic purpura, autoimmune		HP:0001892	OMIM:188030	IEA					P	HPO:iea[2009-02-17]
OMIM:188030	Thrombocytopenic purpura, autoimmune		HP:0003454	OMIM:188030	IEA					P	HPO:iea[2009-02-17]
OMIM:188030	Thrombocytopenic purpura, autoimmune		HP:0001873	OMIM:188030	IEA					P	HPO:iea[2009-02-17]
OMIM:188030	Thrombocytopenic purpura, autoimmune		HP:0000006	OMIM:188030	TAS					I	HPO:skoehler[2013-05-29]
OMIM:232500	Glycogen storage disease IV		HP:0001399	OMIM:232500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0005576	OMIM:232500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:232500	Glycogen storage disease IV		HP:0001371	PMID:17662246	PCS		1/2			P	HPO:probinson[2024-03-08]
OMIM:232500	Glycogen storage disease IV		HP:0001252	PMID:17662246	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001394	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0002040	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0040081	PMID:17662246	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-08]
OMIM:232500	Glycogen storage disease IV		HP:0001508	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001409	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001789	OMIM:232500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001324	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001265	PMID:17662246	PCS		1/2			P	HPO:probinson[2024-03-08]
OMIM:232500	Glycogen storage disease IV		HP:0003202	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001561	PMID:17662246	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001762	PMID:17662246	PCS		1/2			P	HPO:probinson[2024-03-08]
OMIM:232500	Glycogen storage disease IV		HP:0001541	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001662	PMID:17662246	PCS		1/2			P	HPO:probinson[2024-03-08]
OMIM:232500	Glycogen storage disease IV		HP:0034197	PMID:17662246	PCS		2/2			C	HPO:probinson[2024-03-08]
OMIM:232500	Glycogen storage disease IV		HP:0000969	OMIM:232500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:232500	Glycogen storage disease IV		HP:0002804	OMIM:232500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:232500	Glycogen storage disease IV		HP:0000007	PMID:8613547	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:232500	Glycogen storage disease IV		HP:0001558	PMID:17662246	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001638	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001433	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:232500	Glycogen storage disease IV		HP:0001315	OMIM:232500	IEA					P	HPO:iea[2009-02-17]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0003774	PMID:22387013;PMID:24989131;PMID:32278749	PCS		10/21			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0001495	PMID:22387013;PMID:23956186;PMID:24989131;PMID:32278749	PCS		29/29			P	HPO:probinson[2012-07-18];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0007957	PMID:24989131	PCS		3/9			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0001473	PMID:22387013	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0002540	PMID:32278749	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000083	PMID:22387013;PMID:23956186	PCS		15/19			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0003593	PMID:23956186	PCS		3/7			C	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0001193	PMID:23956186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0030836	PMID:24989131	PCS		9/9			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0011463	PMID:23956186;PMID:24989131;PMID:32278749	PCS		8/17			C	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000938	PMID:24989131	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0009487	PMID:24989131	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0011462	PMID:24989131	PCS		1/9			C	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0001504	PMID:23956186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0006234	PMID:23956186;PMID:24989131;PMID:32278749	PCS		18/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0001225	PMID:23956186	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0001785	OMIM:166300	IEA					P	HPO:iea[2009-02-17]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000776	PMID:23956186	PCS		1/8			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0003621	PMID:23956186;PMID:24989131	PCS		5/16			C	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0030840	PMID:24989131	PCS		9/9			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0001761	PMID:23956186	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0005021	PMID:32278749	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000093	PMID:23956186;PMID:24989131;PMID:32278749	PCS		18/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0012586	PMID:32278749	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0002829	PMID:23956186	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000822	PMID:32278749	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000327	OMIM:166300	IEA					P	HPO:iea[2009-02-17]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000520	PMID:23956186;PMID:32278749	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000006	PMID:22387013	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000347	PMID:32278749	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:166300	Multicentric carpotarsal osteolysis syndrome		HP:0000325	PMID:32278749	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0001187	PMID:23408678	PCS		3/17			P	HPO:probinson[2019-07-13]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0004586	PMID:10976985	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0030268	PMID:10976985	PCS		4/7			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0004322	PMID:10976985	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0001382	OMIM:610967	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0000592	PMID:23408678;PMID:10976985	PCS		2/24			P	HPO:skoehler[2015-04-05];HPO:probinson[2019-07-13];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0003593	PMID:10976985	PCS					C	HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0005084	PMID:23408678;PMID:10976985	PCS		17/23			P	HPO:iea[2009-02-17];HPO:probinson[2019-07-13];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0010485	PMID:23408678	PCS		4/17			P	HPO:probinson[2019-07-13]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0006394	PMID:10976985	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0000938	PMID:10976985	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0000926	PMID:10976985	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0008422	PMID:10976985	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0000703	PMID:10976985	PCS		0/7			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0002757	PMID:10976985	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0002645	PMID:10976985	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0001763	PMID:23408678	PCS		3/17			P	HPO:probinson[2019-07-13]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0000006	PMID:23408678	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2019-07-13]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0000325	PMID:23408678	PCS		10/17			P	HPO:skoehler[2015-04-05];HPO:probinson[2019-07-13]
OMIM:610967	Osteogenesis imperfecta, type V		HP:0002644	OMIM:610967	IEA					P	HPO:iea[2009-02-17]
OMIM:300029	Retinitis pigmentosa 3		HP:0001133	PMID:33467000	PCS		4/5			P	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0007737	PMID:34800980;PMID:33467000	PCS		9/9			P	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0000662	PMID:34800980;PMID:33467000	PCS		9/9			P	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0003596	PMID:33467000	PCS		1/5			C	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0000551	PMID:34800980;PMID:33467000	PCS		8/9			P	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0030529	PMID:33467000	PCS		1/5			P	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0011003	PMID:33467000	PCS		2/5			P	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0034272	PMID:34800980	PCS		4/4			P	HPO:probinson[2022-06-04]
OMIM:300029	Retinitis pigmentosa 3		HP:0011463	PMID:33467000	IEA		4/5			C	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0000613	PMID:33467000	PCS		5/5			P	HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0007663	PMID:34800980;PMID:33467000	PCS		9/9			P	HPO:probinson[2022-05-20];HPO:probinson[2020-07-24];HPO:probinson[2022-05-20]
OMIM:300029	Retinitis pigmentosa 3		HP:0001417	PMID:26143542	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-24]
OMIM:300029	Retinitis pigmentosa 3		HP:0000510	PMID:34800980	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-24];HPO:probinson[2022-05-20]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000112	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000431	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0001156	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0003102	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0004322	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000083	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0002091	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000829	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000518	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000506	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000508	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000998	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0000007	OMIM:247410	IEA					I	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0006521	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0001004	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:247410	Lymphedema-Hypoparathyroidism syndrome		HP:0001634	OMIM:247410	IEA					P	HPO:iea[2009-02-17]
OMIM:191950	Urticaria, familial localized heat		HP:0001025	OMIM:191950	IEA					P	HPO:iea[2009-02-17]
OMIM:191950	Urticaria, familial localized heat		HP:0000006	OMIM:191950	IEA					I	HPO:iea[2009-02-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000175	PMID:24462371	PCS		5/13			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0003577	PMID:24462371	PCS		13/13			C	HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000365	PMID:24462371	PCS		10/11			P	HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000518	PMID:24462371	PCS		4/10			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000790	PMID:24462371	PCS		4/7			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000568	PMID:24462371	PCS		8/11			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000612	PMID:24462371	PCS		9/11			P	HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000006	PMID:24462371	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000204	PMID:24462371	PCS		4/13			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0001249	PMID:24462371	PCS		6/6			P	HPO:skoehler[2014-05-04];HPO:probinson[2023-01-17]
OMIM:120433	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or impaired intellectual development		HP:0000567	PMID:24462371	PCS		8/10			P	HPO:probinson[2023-01-17]
OMIM:243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0000403	PMID:6611555	PCS					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-10]
OMIM:243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0000007	OMIM:243110	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0006532	PMID:6611555	PCS					P	HPO:iea[2009-02-17]
OMIM:243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0001417	OMIM:243110	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0001510	PMID:6611555	PCS					P	HPO:iea[2009-02-17]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000252	PMID:28584052;PMID:28302723	PCS		2/5			P	HPO:probinson[2021-09-28];HPO:skoehler[2019-04-18];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000194	PMID:28302723	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0001263	PMID:28584052	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000639	PMID:28584052	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0001419	PMID:28302723	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0012471	PMID:28584052	PCS		2/2			P	HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000646	PMID:28584052	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0008499	PMID:28584052	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000316	PMID:28584052	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0001647	PMID:28584052	PCS		1/2			P	HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000219	PMID:28302723	PCS		1/3			P	HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0004209	PMID:28302723	PCS		3/3			P	HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0030084	PMID:28584052	PCS		2/2			P	HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0008734	PMID:28302723	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000664	PMID:28302723	PCS		1/3		HP:0012825	P	HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000047	PMID:28302723	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0001249	PMID:28302723	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000028	OMIM:300997	TAS					P	HPO:skoehler[2019-04-18]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0002236	PMID:28302723	PCS		1/3			P	HPO:probinson[2021-09-28]
OMIM:300997	Intellectual developmental disorder, X-linked 106		HP:0000369	PMID:28584052	PCS		2/2			P	HPO:probinson[2021-09-28]
OMIM:619957	Attention deficit-hyperactivity disorder 8		HP:0011463	PMID:34702855	PCS		3/3			C	HPO:probinson[2022-08-21]
OMIM:619957	Attention deficit-hyperactivity disorder 8		HP:0011342	PMID:34702855	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619957	Attention deficit-hyperactivity disorder 8		HP:0000007	PMID:34702855	PCS					I	HPO:probinson[2022-08-21]
OMIM:619957	Attention deficit-hyperactivity disorder 8		HP:0007018	PMID:34702855	PCS	HP:0011463	3/3		HP:0012828	P	HPO:probinson[2022-08-21]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000486	PMID:29267967	PCS		3/7			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0002188	PMID:29267967	PCS		1/10			P	HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000243	PMID:29267967	PCS		1/10			P	HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001250	PMID:29267967	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0002120	PMID:29267967	PCS		2/10			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0003593	PMID:29267967	PCS					C	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001251	PMID:29267967	PCS		2/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000639	PMID:29267967	PCS		2/9			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000817	PMID:29267967	PCS		2/9			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000718	PMID:29267967	PCS		3/7			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000218	PMID:29267967	PCS		1/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000752	PMID:29267967	PCS		3/7			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000278	PMID:29267967	PCS		2/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000377	PMID:29267967	PCS		1/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001249	PMID:29267967	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0002236	PMID:29267967	PCS		1/8			P	HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001347	PMID:29267967	PCS		3/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000456	PMID:29267967	PCS		1/8			P	HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000431	PMID:29267967	PCS		1/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001344	PMID:29267967	PCS		3/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000750	PMID:29267967	PCS		10/10			P	HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0002079	PMID:29267967	PCS		1/10			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0031936	PMID:29267967	PCS		4/10			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001263	PMID:29267967	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0002194	PMID:29267967	PCS		6/6			P	HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001419	PMID:29267967	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000729	PMID:29267967	PCS		4/7			P	HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000348	PMID:29267967	PCS		2/8			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0000648	PMID:29267967	PCS		1/9			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001257	PMID:29267967	PCS		2/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:300983	Intellectual developmental disorder, X-linked 104		HP:0001337	PMID:29267967	PCS		2/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2021-09-27]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002664	PMID:7747773;PMID:2586363	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000365	PMID:35637708;PMID:35464843	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001212	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000486	PMID:19204439;PMID:22991675	PCS		2/2			P	HPO:probinson[2022-08-19];HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0005895	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0004322	PMID:35464843;PMID:22991675	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002020	PMID:35637708;PMID:19204439	PCS		2/2			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0003593	PMID:19204439	PCS		1/1			C	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0010442	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000518	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0010055	PMID:35637708;PMID:35464843;PMID:34795756;PMID:10573006	PCS		15/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0008897	OMIM:180849	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000752	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002414	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0003745	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					I	HPO:iea[2011-04-07]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002019	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001601	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002553	PMID:19204439;PMID:34795756	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002311	ISBN-13:978-0721606156;PMID:22991675	PCS		11/11			P	HPO:probinson[2022-08-19];HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000494	PMID:19204439;PMID:34795756;PMID:22991675	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000252	PMID:35464843;PMID:10573006	PCS		7/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0005301	PMID:10573006	PCS		1/4			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000490	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0003083	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0010314	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0010562	PMID:35464843	PCS		2/5			P	HPO:iea[2012-04-24];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000767	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002705	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000527	PMID:34795756	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0004209	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002700	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002788	http://www.ncbi.nlm.nih.gov/books/NBK1526/;PMID:16868563	PCS	HP:0003593				P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000520	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000006	PMID:7630403	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000369	PMID:34795756	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000126	PMID:35637708	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0031207	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0003577	PMID:35637708;PMID:10573006;PMID:22991675	PCS		6/6			C	HPO:probinson[2022-08-19];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000189	PMID:10573006	PCS		3/3			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002000	PMID:22991675	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0003298	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001274	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0004383	PMID:10573006	PCS		1/4			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0006297	OMIM:180849	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011087	PMID:22991675	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0008872	PMID:10573006	PCS		4/4			P	HPO:iea[2012-04-24];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000579	PMID:19204439	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002999	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000736	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000219	PMID:35637708	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000218	PMID:35464843;PMID:22991675	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002236	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001561	PMID:16868563	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000750	PMID:34795756	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002650	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002098	http://www.ncbi.nlm.nih.gov/books/NBK1526/;PMID:16868563	PCS	HP:0003623				P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001680	PMID:35464843	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001042	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0010775	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011229	PMID:34795756	PCS		6/6			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0100710	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000508	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0030890	PMID:35464843	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001956	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS	HP:0003621				P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002007	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0008107	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001159	PMID:19204439	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0009836	PMID:22991675	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000589	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000501	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000347	PMID:35637708;PMID:34795756	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0009715	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000742	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000286	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001371	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001250	PMID:34795756	PCS		0/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000160	PMID:22991675	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001252	PMID:10573006	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011335	PMID:35637708	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002183	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000957	OMIM:180849	TAS					P	HPO:skoehler[2013-05-31]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000319	PMID:35637708	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011220	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000717	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000316	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000954	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000678	PMID:19204439	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002219	PMID:10573006	PCS		4/4			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001643	PMID:35464843;PMID:10573006	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001763	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000278	OMIM:180849	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001007	PMID:34795756	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001249	PMID:35464843;PMID:34795756;PMID:22991675	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0020206	PMID:22991675	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000175	PMID:22991675	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0004411	PMID:22991675	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002353	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002870	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000574	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002750	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011968	PMID:34795756	PCS		2/6			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001382	http://www.ncbi.nlm.nih.gov/books/NBK1526/;OMIM:180849	PCS		20/20			P	HPO:skoehler[2017-07-13];HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001263	PMID:35637708;PMID:35464843;PMID:10573006	PCS		10/10			P	HPO:probinson[2022-08-19];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000294	PMID:35637708;PMID:34795756;ISBN-13:978-0721606156	PCS		15/17			P	HPO:probinson[2022-08-19];HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0034227	PMID:35464843	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002869	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-05-28]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000327	PMID:19204439	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000448	PMID:35464843	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000689	PMID:22991675	PCS		1/1			P	HPO:iea[2012-04-24];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000444	PMID:19204439;PMID:34795756;PMID:22991675	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0008689	PMID:35637708;PMID:19204439	PCS		2/2			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002866	ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-05-28]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000047	PMID:10573006	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0009778	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001655	PMID:10573006	PCS		1/4			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000049	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000260	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002162	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001909	OMIM:180849	IEA					P	HPO:skoehler[2018-10-08]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001508	PMID:10573006	PCS	HP:0003593	4/4			P	HPO:iea[2012-04-24];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001629	PMID:35464843	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011682	PMID:35464843	PCS		1/5			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002317	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001747	PMID:10573006	PCS		2/4			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0009765	PMID:19204439;PMID:10573006;PMID:22991675	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0005306	PMID:19204439	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001347	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0002697	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001762	PMID:34795756	PCS		1/6			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000431	PMID:17942008;PMID:22991675	PCS		11/11			P	HPO:probinson[2022-08-19];HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000270	ISBN-13:978-0721606156	PCS					P	HPO:iea[2009-02-17]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011947	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000273	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0010059	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0011304	PMID:35637708;PMID:35464843;PMID:19204439;PMID:34795756;PMID:10573006;PMID:22991675	PCS		17/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06];HPO:probinson[2022-08-19];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0010066	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS					P	HPO:iea[2012-04-24]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001518	PMID:10573006	PCS	HP:0003577	2/4			P	HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001631	PMID:8599359	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-19]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001510	PMID:34795756	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0000028	PMID:35464843	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:180849	Rubinstein-Taybi syndrome 1		HP:0001634	PMID:19204439	PCS		1/1			P	HPO:probinson[2022-08-19]
OMIM:226950	Epiphyseal dysplasia of femoral head, myopia, and deafness		HP:0000365	OMIM:226950	IEA					P	HPO:iea[2009-02-17]
OMIM:226950	Epiphyseal dysplasia of femoral head, myopia, and deafness		HP:0000007	OMIM:226950	IEA					I	HPO:iea[2009-02-17]
OMIM:226950	Epiphyseal dysplasia of femoral head, myopia, and deafness		HP:0011003	OMIM:226950	IEA					P	HPO:iea[2009-02-17]
OMIM:226950	Epiphyseal dysplasia of femoral head, myopia, and deafness		HP:0010574	OMIM:226950	IEA					P	HPO:skoehler[2015-01-21]
OMIM:226950	Epiphyseal dysplasia of femoral head, myopia, and deafness		HP:0002656	OMIM:226950	IEA					P	HPO:skoehler[2015-01-21]
OMIM:218100	Cranial nerves, congenital paresis of		HP:0010628	OMIM:218100	IEA					P	HPO:iea[2009-02-17]
OMIM:218100	Cranial nerves, congenital paresis of		HP:0000007	OMIM:218100	IEA					I	HPO:iea[2009-02-17]
OMIM:218100	Cranial nerves, congenital paresis of		HP:0000377	OMIM:218100	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000286	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000343	OMIM:269921	TAS					P	HPO:probinson[2012-05-01]
OMIM:269921	Sialuria		HP:0410156	PMID:10330343	PCS		1/1			P	HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0005257	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000023	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0001250	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0002162	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0003593	PMID:10330343	PCS		2/2			C	HPO:probinson[2022-10-19];HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0002240	PMID:10330343	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0000280	PMID:10330343	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0000319	OMIM:269921	TAS					P	HPO:probinson[2012-05-01]
OMIM:269921	Sialuria		HP:0001507	PMID:10330343	PCS		0/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0011220	OMIM:269921	TAS					P	HPO:skoehler[2012-10-17]
OMIM:269921	Sialuria		HP:0000316	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000219	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0001847	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000218	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000158	PMID:10330343	PCS		1/3			P	HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0002557	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000256	PMID:10330343	PCS		1/3			P	HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0001744	PMID:10330343	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0001007	PMID:10330343	PCS		1/3			P	HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0000431	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0002650	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0002230	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0001263	PMID:10330343	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0004691	OMIM:269921	TAS					P	HPO:probinson[2012-05-01]
OMIM:269921	Sialuria		HP:0010535	OMIM:269921	IEA					P	HPO:skoehler[2010-06-18]
OMIM:269921	Sialuria		HP:0007010	PMID:10330343	PCS		1/3			P	HPO:probinson[2022-10-19]
OMIM:269921	Sialuria		HP:0000629	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0001538	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000664	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0002007	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0007018	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000369	OMIM:269921	IEA					P	HPO:iea[2009-02-17]
OMIM:269921	Sialuria		HP:0000006	PMID:10330343	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-19]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0002840	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0033605	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0002783	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0002240	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0410395	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0003593	PMID:36736301	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0032256	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0034752	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0100721	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0032261	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0032283	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0001508	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0001903	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0000957	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0001945	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0030381	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0500265	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0001744	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0040218	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0002014	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0410389	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0005403	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0001882	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0020086	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0020087	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0003261	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0002090	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0011274	PMID:36736301	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0001217	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0000246	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0001873	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0430108	PMID:36736301	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0002566	PMID:36736301	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620668	Immunodeficiency 117, mycobacteriosis, autosomal recessive		HP:0000006	PMID:36736301	PCS					I	ORCID:0000-0002-0736-9199[2024-07-18]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0002013	PMID:11231969	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0000848	PMID:11231969	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0002153	PMID:11231969	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0000859	PMID:11231969	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0001944	PMID:11231969	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0002902	PMID:11231969	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0000007	PMID:8640238	PCS					I	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0001942	PMID:11231969	PCS		1/1			P	HPO:probinson[2023-03-04]
OMIM:620126	Pseudohypoaldosteronism, type IB3, autosomal recessive		HP:0003623	PMID:11231969	PCS		1/1			C	HPO:probinson[2023-03-04]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0012156	PMID:7436463	PCS		0/2			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-09]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0001442	PMID:23589569	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-07-14]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0000980	PMID:7436463	PCS		2/2			P	HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-09]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0000979	PMID:9766805	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0003593	PMID:7436463	PCS		2/2			C	HPO:probinson[2024-03-09]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0002240	PMID:7436463	PCS		2/2			P	HPO:probinson[2024-03-09]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0001945	PMID:9766805	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0001978	PMID:7436463	PCS		2/2			P	HPO:probinson[2024-03-09]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0001744	PMID:7436463	PCS		2/2			P	HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-09]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0005547	PMID:7436463	PCS					P	HPO:probinson[2009-02-17];HPO:lccarmody[2018-10-03]
OMIM:254450	Myelofibrosis with myeloid metaplasia, somatic		HP:0011974	PMID:9766805	PCS		2/2			P	HPO:probinson[2012-07-18];HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-09]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002982	PMID:19816730	PCS		1/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001498	PMID:24300288	PCS		2/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002980	PMID:19816730	PCS		1/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000882	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0003311	PMID:24300288	PCS		1/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001376	PMID:19816730	PCS		7/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0010049	PMID:24300288	PCS		2/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000280	PMID:24300288	PCS		2/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0012428	PMID:19816730	PCS		3/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0034414	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0003270	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000914	PMID:19816730	PCS		14/15			P	HPO:skoehler[2014-06-24];HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0011463	PMID:24300288	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000319	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002938	PMID:19816730;PMID:24300288	PCS		16/16			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-03];ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0008897	OMIM:223800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001769	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000911	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002857	PMID:19816730;PMID:24300288	PCS		16/17			P	HPO:skoehler[2015-04-05];HP:probinson[2019-03-03];ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001169	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001763	PMID:19816730	PCS		3/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001249	PMID:24300288	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0004997	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0003521	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000252	PMID:24300288	PCS		1/2			P	HPO:probinson[2009-02-17];HPO:probinson[2024-06-27]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001344	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000574	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002035	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0012385	OMIM:223800	TAS					P	HPO:skoehler[2013-10-22]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000926	PMID:24300288;PMID:12491225	PCS		12/12			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-03];ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000007	OMIM:223800	TAS					I	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000920	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0004209	PMID:19816730	PCS		5/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000768	PMID:19816730	PCS		13/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000884	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002942	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0006589	PMID:19816730	PCS		15/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002866	PMID:24300288	PCS		1/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0004568	PMID:24300288	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2024-06-27]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0003016	PMID:19816730	PCS		15/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0008905	PMID:24300288	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001552	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001156	PMID:19816730	PCS		15/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002684	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002681	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0003375	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0010743	PMID:24300288	PCS		2/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0010230	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0006450	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002515	PMID:24300288	PCS		1/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000154	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002213	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002650	PMID:19816730;PMID:24300288	PCS		13/17			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-03];ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0001762	PMID:19816730	PCS		1/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002970	PMID:19816730	PCS		1/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002692	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0004991	PMID:19816730	PCS		14/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000470	PMID:19816730;PMID:24300288	PCS		16/17			P	HPO:probinson[2009-02-17];HP:probinson[2019-03-03];ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0003183	PMID:24300288	PCS		2/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0011344	OMIM:223800	TAS					P	HPO:probinson[2015-02-23]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0003180	PMID:24300288	PCS		1/2			P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0002808	PMID:19816730	PCS		8/15			P	HP:probinson[2019-03-03]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0008786	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000664	PMID:24300288	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-26]
OMIM:223800	Dyggve-Melchior-Clausen disease		HP:0000303	OMIM:223800	TAS					P	HPO:probinson[2009-02-17]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0000164	PMID:26151409	PCS		3/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0002079	PMID:26151409	PCS		8/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0031936	PMID:26151409	PCS		5/8			P	HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001272	PMID:26151409	PCS		5/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001263	PMID:26151409	PCS		7/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0003593	PMID:26151409	PCS		4/8			C	HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001251	PMID:26151409	PCS		8/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001508	PMID:26151409	PCS		1/8			P	HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0011463	PMID:26151409	PCS		4/8			C	HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0000007	PMID:26151409	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0003429	PMID:26151409	PCS		8/8			P	HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001257	PMID:26151409	PCS		6/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0002415	PMID:26151409	PCS					P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001337	PMID:26151409	PCS		8/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0000545	PMID:26151409	PCS		3/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001249	PMID:26151409	PCS		6/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-04-09]
OMIM:616494	Leukodystrophy, hypomyelinating, 11		HP:0001336	PMID:26151409	PCS		1/8			P	HPO:probinson[2022-04-09]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000164	OMIM:617952	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0002980	PMID:29358272	PCS		4/4			P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000750	OMIM:617952	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000431	OMIM:617952	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0004586	PMID:29358272	PCS					P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0001382	OMIM:617952;PMID:29358272	PCS		20/20			P	HP:probinson[2018-05-12];HPO:skoehler[2018-10-08]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000592	PMID:29358272	PCS	HP:0003593	4/4			P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0040160	PMID:29358272	PCS					P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0001270	OMIM:617952	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0001537	PMID:29358272	PCS	HP:0003577	1/4			P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000007	PMID:29358272	PCS					I	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000337	PMID:29358272	PCS					P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0002757	PMID:29358272	PCS	HP:0003593	4/4			P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0006487	PMID:29358272	PCS					P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000527	OMIM:617952	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0002645	PMID:29358272	PCS		3/4			P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0002953	OMIM:617952	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000883	PMID:29358272	PCS					P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0002753	PMID:29358272	PCS					P	HP:probinson[2018-05-12]
OMIM:617952	Osteogenesis imperfecta, type XVIII		HP:0000347	OMIM:617952	IEA					P	HPO:skoehler[2018-10-08]
OMIM:219550	Cysteine peptiduria		HP:0010918	PMID:4730204	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:219550	Cysteine peptiduria		HP:0000007	OMIM:219550	IEA					I	HPO:iea[2009-02-17]
OMIM:219550	Cysteine peptiduria		HP:0010895	PMID:4730204	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:219550	Cysteine peptiduria		HP:0001249	PMID:4730204	PCS					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-02]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0200150	OMIM:147480	TAS					P	HPO:skoehler[2013-06-13]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0200148	OMIM:147480	TAS					P	HPO:skoehler[2013-06-13]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0000989	OMIM:147480	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0001406	OMIM:147480	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0025116	OMIM:147480	TAS					P	HPO:skoehler[2017-07-13]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0002910	OMIM:147480	IEA					P	HPO:skoehler[2010-06-20]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0000006	OMIM:147480	IEA					I	HPO:skoehler[2010-06-19]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0000952	OMIM:147480	IEA					P	HPO:skoehler[2018-10-08]
OMIM:147480	Cholestasis, intrahepatic, of pregnancy, 1		HP:0001622	OMIM:147480	IEA					P	HPO:skoehler[2010-06-18]
OMIM:167750	Pancreas, annular		HP:0100867	OMIM:167750	IEA					P	HPO:skoehler[2010-06-18]
OMIM:167750	Pancreas, annular		HP:0001734	OMIM:167750	IEA					P	HPO:iea[2009-02-17]
OMIM:167750	Pancreas, annular		HP:0005250	OMIM:167750	IEA					P	HPO:iea[2009-02-17]
OMIM:167750	Pancreas, annular		HP:0000006	OMIM:167750	IEA					I	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0008969	PMID:20853184	IEA		1/2			P	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001276	PMID:16964263	PCS		4/4			P	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002067	PMID:16964263	PCS		4/4			P	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001332	PMID:20853184	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001250	OMIM:606693	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002385	OMIM:606693	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002063	PMID:16964263	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001251	OMIM:606693	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000738	PMID:16964263	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0011462	PMID:16964263	PCS		2/3			C	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000718	OMIM:606693	IEA					P	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000514	PMID:16964263;PMID:20853184	PCS		3/5			P	HPO:probinson[2021-02-14];HPO:skoehler[2012-10-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002936	OMIM:606693	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000458	OMIM:606693	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001348	PMID:20853184	IEA		2/2			P	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001347	OMIM:606693	IEA					P	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000473	OMIM:606693	TAS					P	HPO:skoehler[2013-11-28]
OMIM:606693	Kufor-Rakeb syndrome		HP:0003621	PMID:16964263	PCS		1/3			C	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002015	PMID:20853184	PCS		1/2			P	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001300	OMIM:606693	IEA					P	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002375	PMID:20853184	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000298	PMID:20853184	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001288	PMID:20853184	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0003487	PMID:16964263;PMID:20853184	PCS		5/6			P	HPO:probinson[2021-02-14];HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001260	PMID:20853184	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002172	OMIM:606693	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0030902	PMID:16964263	PCS		3/4			P	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0012378	PMID:16964263	PCS					P	HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000605	PMID:16964263;PMID:20853184	PCS		5/6			P	HPO:probinson[2021-02-14];HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000726	PMID:16964263	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0004409	OMIM:606693	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000007	PMID:16964263	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0000725	OMIM:606693	IEA					P	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002548	OMIM:606693	TAS					P	HPO:probinson[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001258	OMIM:606693	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002425	OMIM:606693	IEA					P	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0002304	OMIM:606693	IEA					P	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001257	OMIM:606693	IEA					P	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001337	PMID:16964263	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-14]
OMIM:606693	Kufor-Rakeb syndrome		HP:0003678	OMIM:606693	IEA					C	HPO:iea[2009-02-17]
OMIM:606693	Kufor-Rakeb syndrome		HP:0001336	PMID:16964263	PCS		3/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-14]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0003750	OMIM:611489	IEA					P	HPO:iea[2009-02-17]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0003581	PMID:10634411	PCS		1/1			C	HPO:probinson[2022-10-20]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:6000243	PMID:11502797	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0012378	OMIM:611489	IEA					P	HPO:skoehler[2019-09-07]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0012364	PMID:10634411	PCS		1/1			P	HPO:probinson[2022-10-20]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0008163	PMID:10634411	PCS		1/1			P	HPO:probinson[2022-10-20]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0001903	PMID:10634411	PCS		1/1			P	HPO:probinson[2022-10-20]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0000822	OMIM:611489	IEA					P	HPO:iea[2009-02-17]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0000007	PMID:10634411	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-20]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0002900	PMID:10634411	PCS		1/1			P	HPO:probinson[2022-10-20]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0002615	PMID:10634411	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-20]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0000006	OMIM:611489	IEA					I	HPO:iea[2009-02-17]
OMIM:611489	Corticosteroid-binding globulin deficiency		HP:0025406	PMID:10634411	PCS		1/1			P	HPO:probinson[2022-10-20]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000286	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0002389	PMID:32627184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000483	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001256	PMID:37850357;PMID:35451551;PMID:32627184	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000089	PMID:32627184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0004322	PMID:32627184	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000122	PMID:32627184	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000480	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001252	PMID:37850357;PMID:35451551;PMID:32627184	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0012745	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0045075	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0033725	PMID:37850357	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000958	PMID:32627184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000639	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000518	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000319	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0011463	PMID:32627184	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001647	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0002616	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000316	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001888	PMID:37850357;PMID:32627184	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000678	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0002779	PMID:35451551;PMID:32627184	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001643	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000278	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001642	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000358	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0003623	PMID:35451551	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001385	PMID:32627184	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000494	PMID:37850357;PMID:35451551;PMID:32627184	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0011968	PMID:37850357;PMID:35451551;PMID:32627184	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001382	PMID:32627184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001263	PMID:35451551;PMID:32627184	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0011800	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0010880	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0034396	PMID:37850357	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001537	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000403	PMID:35451551;PMID:32627184	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000768	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000685	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000369	PMID:37850357;PMID:35451551;PMID:32627184	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000006	PMID:32627184	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000582	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000384	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0003577	PMID:37850357	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000343	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001156	PMID:35451551;PMID:32627184	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000023	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000540	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0030674	PMID:32627184	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0002282	PMID:37850357;PMID:32627184	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001270	PMID:37850357;PMID:35451551;PMID:32627184	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0040080	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001629	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001903	PMID:37850357;PMID:35451551;PMID:32627184	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000414	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000612	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000219	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0002119	PMID:37850357	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000218	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001320	PMID:35451551;PMID:32627184	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000076	PMID:32627184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000750	PMID:37850357;PMID:35451551;PMID:32627184	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001882	PMID:37850357;PMID:32627184	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000194	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0005484	PMID:37850357;PMID:35451551;PMID:32627184	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0034323	PMID:32627184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0005280	PMID:37850357;PMID:35451551;PMID:32627184	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0011272	PMID:35451551	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000426	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001714	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0002205	PMID:35451551;PMID:32627184	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001159	PMID:35451551;PMID:32627184	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001873	PMID:37850357;PMID:35451551;PMID:32627184	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001876	PMID:32627184	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0001513	PMID:32627184	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620654	Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies		HP:0000347	PMID:37850357;PMID:35451551;PMID:32627184	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0003025	OMIM:610797	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0001382	OMIM:610797	TAS					P	HPO:probinson[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0003275	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0004231	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0010048	OMIM:610797	TAS					P	HPO:probinson[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0009196	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0001507	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0009465	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0000007	OMIM:610797	TAS					I	HPO:probinson[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0100807	OMIM:610797	TAS					P	HPO:probinson[2012-07-15]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0002857	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0004209	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0002656	OMIM:610797	TAS					P	HPO:probinson[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0001763	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0008802	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:610797	Epiphyseal dysplasia, Baumann type		HP:0003799	OMIM:610797	IEA					P	HPO:iea[2009-02-17]
OMIM:615837	Deafness, autosomal recessive 101		HP:0008619	PMID:24619944	PCS		3/3			P	HPO:skoehler[2014-10-17];HPO:probinson[2022-10-23]
OMIM:615837	Deafness, autosomal recessive 101		HP:0001751	PMID:24619944	PCS		0/3			P	HPO:probinson[2022-10-23]
OMIM:615837	Deafness, autosomal recessive 101		HP:0011463	PMID:24619944	PCS		3/3			C	HPO:probinson[2022-10-23]
OMIM:615837	Deafness, autosomal recessive 101		HP:0000007	PMID:24619944	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:615837	Deafness, autosomal recessive 101		HP:0000505	PMID:24619944	PCS		0/3			P	HPO:probinson[2022-10-23]
OMIM:615604	L-ferritin deficiency, dominant and recessive		HP:0012452	PMID:23940258	PCS		1/1			P	HPO:probinson[2019-04-20];HPO:probinson[2019-04-20]
OMIM:615604	L-ferritin deficiency, dominant and recessive		HP:0003621	PMID:23940258	IEA		1/1			C	HPO:probinson[2022-03-18]
OMIM:615604	L-ferritin deficiency, dominant and recessive		HP:0012343	PMID:15173247;PMID:23940258	PCS		2/2			P	HPO:probinson[2022-03-18];HPO:probinson[2019-04-20];HPO:probinson[2019-04-20]
OMIM:615604	L-ferritin deficiency, dominant and recessive		HP:0001596	PMID:15173247;OMIM:615604	PCS		10/11			P	HPO:probinson[2022-03-18];HPO:probinson[2019-04-20]
OMIM:615604	L-ferritin deficiency, dominant and recessive		HP:0002197	PMID:23940258	PCS		1/2			P	HPO:probinson[2022-03-18];HPO:probinson[2019-04-20];HPO:probinson[2019-04-20]
OMIM:615604	L-ferritin deficiency, dominant and recessive		HP:0000007	PMID:23940258	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2019-04-20]
OMIM:615604	L-ferritin deficiency, dominant and recessive		HP:0000006	PMID:15173247	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2022-03-18]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002344	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0005216	PMID:29498153	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001771	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0003676	PMID:27231142	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0003236	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002540	PMID:29498153	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002067	PMID:27231142	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001332	PMID:27231142;PMID:29498153	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001272	PMID:27231142	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001252	PMID:29498153	PCS		1/1			P	HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0003593	PMID:29498153	PCS		1/1			C	HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0012407	PMID:27231142	PCS		3/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0012048	PMID:27231142	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0000737	PMID:27231142	PCS		3/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0000338	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0000975	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0006895	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0007325	PMID:27231142	PCS		6/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0000256	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001249	PMID:27231142	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001348	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001347	PMID:27231142	PCS		4/18			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27];HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002179	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0008936	PMID:27231142	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0000252	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002312	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002059	PMID:27231142	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002650	PMID:27231142	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001300	PMID:27231142	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002375	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001344	PMID:27231142	PCS		1/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001288	PMID:27231142	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002376	PMID:27231142	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0003487	PMID:27231142	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0003121	PMID:27231142	PCS		3/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0002451	PMID:27231142	PCS		3/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001263	PMID:27231142;PMID:29498153	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0005484	PMID:27231142	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0011448	PMID:27231142	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0032097	PMID:27231142;PMID:29498153	PCS		3/10			P	HP:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0030890	PMID:27231142	PCS		10/10			P	HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0000007	PMID:27231142	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0030051	PMID:27231142	PCS		4/9			P	HP:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001257	PMID:27231142;PMID:29498153	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:617013	Hypermanganesemia with dystonia 2		HP:0001337	PMID:27231142	PCS		1/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-02-27]
OMIM:607200	Thyroid dyshormonogenesis 6		HP:0000007	OMIM:607200	IEA					I	HPO:skoehler[2010-06-19]
OMIM:607200	Thyroid dyshormonogenesis 6		HP:0000821	OMIM:607200	IEA					P	HPO:skoehler[2010-06-19]
OMIM:607200	Thyroid dyshormonogenesis 6		HP:0000851	OMIM:607200	IEA					P	HPO:skoehler[2010-06-19]
OMIM:608133	Retinitis pigmentosa 7		HP:0001133	OMIM:608133	TAS					P	HPO:skoehler[2015-01-04]
OMIM:608133	Retinitis pigmentosa 7		HP:0000662	PMID:25447119	PCS	HP:0003581				P	HPO:probinson[2017-12-22]
OMIM:608133	Retinitis pigmentosa 7		HP:0000580	PMID:25447119	PCS					P	HPO:probinson[2017-12-22]
OMIM:608133	Retinitis pigmentosa 7		HP:0000007	OMIM:608133	TAS					I	HPO:skoehler[2015-12-30]
OMIM:608133	Retinitis pigmentosa 7		HP:0007830	OMIM:608133	TAS					P	HPO:probinson[2013-02-23]
OMIM:608133	Retinitis pigmentosa 7		HP:0000510	OMIM:608133	TAS					P	HPO:probinson[2013-02-23]
OMIM:608133	Retinitis pigmentosa 7		HP:0007843	PMID:25447119	PCS					P	HPO:probinson[2017-12-22]
OMIM:608133	Retinitis pigmentosa 7		HP:0000512	OMIM:608133	TAS					P	HPO:probinson[2013-02-23]
OMIM:608133	Retinitis pigmentosa 7		HP:0000006	PMID:25447119	PCS					I	HPO:probinson[2017-12-22]
OMIM:608133	Retinitis pigmentosa 7		HP:0000533	OMIM:608133	TAS		HP:0040283			P	HPO:skoehler[2015-07-19]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000483	PMID:18812405	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001773	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002463	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0004322	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001250	PMID:17847001	PCS	HP:0011463	1/1			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001250	PMID:18812405	PCS		2/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0003196	OMIM:156200	TAS					P	HPO:skoehler[2012-11-19]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0003593	PMID:18812405	IEA		2/2			C	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002020	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001251	PMID:18812405	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0034187	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002937	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000718	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000316	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0008897	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0025336	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000158	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000278	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002019	PMID:18812405	PCS		2/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001249	PMID:18812405	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002553	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0003763	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000054	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000252	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001385	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000574	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000331	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0011968	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002591	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000691	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001263	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0011800	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0008081	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0100023	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000729	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0005819	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000448	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000527	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002307	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0004209	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001852	PMID:17847001	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000565	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000369	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000248	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000006	PMID:18812405	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000687	PMID:18812405	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0410018	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000540	PMID:18812405	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002000	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002162	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001270	PMID:18812405	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0010306	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000817	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0008551	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000739	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000414	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000337	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000219	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000736	PMID:18812405	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002714	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000411	OMIM:156200	TAS					P	HPO:skoehler[2012-11-19]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000378	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000457	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000154	PMID:18812405	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0001320	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0004279	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002650	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0005445	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000232	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000194	OMIM:156200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002373	PMID:17847001	PCS	HP:0003593	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0005484	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0012760	PMID:17847001	PCS		1/1			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000748	PMID:18812405	PCS		2/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0007333	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000505	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0100716	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0002007	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000545	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000347	OMIM:156200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:156200	Intellectual developmental disorder, autosomal dominant 1		HP:0000303	PMID:18812405	PCS		1/2			P	HPO:probinson[2022-05-22]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000384	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000582	PMID:28920961	PCS		3/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0003577	PMID:28920961	PCS		3/3			C	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001399	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001773	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000486	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000089	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001250	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001252	PMID:28920961	PCS		2/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0040262	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0031624	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0034185	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000316	PMID:28920961	PCS		2/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0020045	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000455	PMID:28920961	PCS		2/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000278	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001249	PMID:28920961	PCS		2/2			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000456	PMID:28920961	PCS		3/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000154	PMID:28920961	PCS		2/2			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000252	PMID:28920961	PCS		3/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001684	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0005564	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0011968	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0012736	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0012165	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000709	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000629	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000508	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000646	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000965	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000822	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001537	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001558	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000403	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0004209	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0002205	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0001510	PMID:28920961	IEA		3/3			P	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000006	PMID:28920961	PCS					I	HPO:probinson[2022-04-17]
OMIM:619758	Tessadori-van Haaften neurodevelopmental syndrome 1		HP:0000369	PMID:28920961	PCS		1/3			P	HPO:probinson[2022-04-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0003577	PMID:27549381	PCS		2/2			C	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000463	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001252	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001274	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0010806	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0008070	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001629	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0012471	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0006297	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0003307	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0025578	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0030084	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000358	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001545	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0002212	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000175	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000494	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001264	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000252	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001762	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000431	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000232	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000298	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001263	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0012385	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000506	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000348	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0200055	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000400	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000003	PMID:27549381	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001510	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0001873	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000201	PMID:27549381	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:619980	Braddock-Carey syndrome 1		HP:0000006	PMID:27549381	PCS					I	HPO:probinson[2022-08-17]
OMIM:600209	Exostoses, multiple, type III		HP:0002762	OMIM:600209	IEA					P	HPO:iea[2009-02-17]
OMIM:600209	Exostoses, multiple, type III		HP:0000006	OMIM:600209	IEA					I	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0002102	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0033726	PMID:26342222	PCS		700/1827			P	HPO:probinson[2021-06-13]
OMIM:152700	Systemic lupus erythematosus		HP:0000123	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0000992	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0001882	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0001250	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0003493	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0025300	OMIM:152700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:152700	Systemic lupus erythematosus		HP:0000709	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0001878	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0001701	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0002725	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0003613	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0001873	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0000006	OMIM:152700	IEA					I	HPO:iea[2009-02-17]
OMIM:152700	Systemic lupus erythematosus		HP:0001369	OMIM:152700	IEA					P	HPO:iea[2009-02-17]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0004325	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000343	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0001290	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000280	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0008551	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000316	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000337	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000219	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0002714	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0030084	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0001249	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0001007	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0005469	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000494	OMIM:615162	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0009928	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000232	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0003022	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0001263	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000272	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000007	PMID:20950399	PCS					I	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000348	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000664	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000369	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000347	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:615162	Intellectual developmental disorder, autosomal recessive 35		HP:0000445	PMID:20950399	PCS					P	HPO:probinson[2015-05-10]
OMIM:261400	Peroneus tertius muscle, absence of		HP:0003011	OMIM:261400	IEA					P	HPO:iea[2009-02-17]
OMIM:261400	Peroneus tertius muscle, absence of		HP:0009027	OMIM:261400	TAS					P	HPO:probinson[2015-02-03]
OMIM:261400	Peroneus tertius muscle, absence of		HP:0000007	OMIM:261400	TAS					I	HPO:probinson[2009-02-17]
OMIM:209970	Beemer lethal malformation syndrome		HP:0000431	OMIM:209970	IEA					P	HPO:iea[2009-02-17]
OMIM:209970	Beemer lethal malformation syndrome		HP:0000062	OMIM:209970	IEA					P	HPO:iea[2009-02-17]
OMIM:209970	Beemer lethal malformation syndrome		HP:0000924	OMIM:209970	IEA					P	HPO:iea[2009-02-17]
OMIM:209970	Beemer lethal malformation syndrome		HP:0000007	OMIM:209970	IEA					I	HPO:iea[2009-02-17]
OMIM:209970	Beemer lethal malformation syndrome		HP:0000238	OMIM:209970	IEA					P	HPO:iea[2009-02-17]
OMIM:209970	Beemer lethal malformation syndrome		HP:0030680	OMIM:209970	IEA					P	HPO:iea[2009-02-17]
OMIM:209970	Beemer lethal malformation syndrome		HP:0001873	OMIM:209970	IEA					P	HPO:iea[2009-02-17]
OMIM:613507	Glycogen storage disease XV		HP:0031319	PMID:20357282	PCS		1/1			P	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0025708	PMID:20357282	PCS		1/1			C	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0001663	PMID:20357282	PCS	HP:0025710	1/1			P	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0004751	PMID:20357282	PCS	HP:0025710	1/1			P	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0003691	PMID:20357282	PCS	HP:0025710	1/1			P	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0012251	PMID:20357282	PCS	HP:0025708	1/1			P	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0000007	PMID:20357282	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0011712	PMID:20357282	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0010872	PMID:20357282	PCS	HP:0025708	1/1			P	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0003803	PMID:20357282	PCS		1/1			P	HPO:probinson[2022-10-30]
OMIM:613507	Glycogen storage disease XV		HP:0001324	PMID:20357282	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:608641	Deafness, autosomal dominant nonsyndromic sensorineural 28		HP:0003676	OMIM:608641	TAS					C	HPO:probinson[2013-12-20]
OMIM:608641	Deafness, autosomal dominant nonsyndromic sensorineural 28		HP:0000407	OMIM:608641	TAS					P	HPO:skoehler[2010-06-18]
OMIM:608641	Deafness, autosomal dominant nonsyndromic sensorineural 28		HP:0000006	OMIM:608641	TAS					I	HPO:skoehler[2009-02-17]
OMIM:233420	46,xy sex reversal 7		HP:0000013	OMIM:233420	TAS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:233420	46,xy sex reversal 7		HP:0012245	PMID:15356051	PCS		6/6			P	HPO:probinson[2013-04-02];HPO:probinson[2022-09-03]
OMIM:233420	46,xy sex reversal 7		HP:0100621	PMID:15356051	PCS	HP:0011462	1/6			P	HPO:probinson[2022-09-03]
OMIM:233420	46,xy sex reversal 7		HP:0000150	OMIM:233420	TAS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:233420	46,xy sex reversal 7		HP:0000150	PMID:15356051	PCS	HP:0003621	2/6			P	HPO:probinson[2022-09-03]
OMIM:233420	46,xy sex reversal 7		HP:0008697	OMIM:233420	TAS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:233420	46,xy sex reversal 7		HP:0000007	PMID:15356051	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:233420	46,xy sex reversal 7		HP:0010464	PMID:15356051	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:233420	46,xy sex reversal 7		HP:0008668	PMID:15356051	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:233420	46,xy sex reversal 7		HP:0009714	OMIM:233420	TAS		HP:0040282			P	HPO:iea[2010-01-19]
OMIM:233420	46,xy sex reversal 7		HP:0000786	OMIM:233420	TAS					P	HPO:skoehler[2012-10-17]
OMIM:617761	Joubert syndrome 31		HP:0000486	PMID:27208211	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0002078	PMID:27208211	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0002079	PMID:27208211	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0000639	PMID:27208211	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0001263	PMID:27208211	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0001252	PMID:27208211	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0000657	PMID:27208211	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0000007	PMID:27208211	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0002419	PMID:27208211	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0002119	PMID:27208211	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0009921	PMID:27208211	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:617761	Joubert syndrome 31		HP:0003623	PMID:27208211	PCS		4/4			C	HPO:probinson[2023-02-11]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0003621	PMID:16960801	PCS		3/8			C	HPO:probinson[2022-09-04]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0011463	PMID:16960801	PCS		1/8			C	HPO:probinson[2022-09-04]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0011462	PMID:16960801	PCS		4/8			C	HPO:probinson[2022-09-04]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0000007	PMID:16960801	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0006520	OMIM:265100	IEA					P	HPO:iea[2009-02-17]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0002091	OMIM:265100	IEA					P	HPO:iea[2009-02-17]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0003677	OMIM:265100	IEA					C	HPO:iea[2009-02-17]
OMIM:265100	Pulmonary alveolar microlithiasis		HP:0006514	OMIM:265100	IEA					P	HPO:iea[2009-02-17]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0002521	PMID:17273964	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0003577	PMID:17273964	PCS		2/4			C	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001596	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001250	PMID:17273964	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001252	PMID:17273964	PCS		3/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0003593	PMID:17273964	PCS		2/4			C	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0045075	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0000958	PMID:17273964	PCS		2/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001508	OMIM:610768	IEA					P	HPO:iea[2009-02-17]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0011123	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0000639	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0002835	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001522	PMID:17273964	PCS		4/4			C	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0000653	PMID:17273964	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001644	PMID:17273964	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001985	PMID:17273964	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0002014	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0003642	PMID:17273964	PCS		4/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0001662	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0002013	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0030781	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0005484	PMID:17273964	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0008064	PMID:17273964	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0000007	PMID:17273964	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0002445	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:610768	Congenital disorder of glycosylation, type Im		HP:0000962	PMID:17273964	PCS		1/4			P	HPO:probinson[2022-05-08]
OMIM:601665	OBESITY		HP:0012340	OMIM:601665	TAS					P	HPO:iea[2015-05-03]
OMIM:601665	OBESITY		HP:0031819	PMID:12872269	PCS					P	HPO:lccarmody[2018-09-25]
OMIM:601665	OBESITY		HP:0000007	OMIM:601665	TAS					I	HPO:skoehler[2015-12-30]
OMIM:601665	OBESITY		HP:0010982	OMIM:601665	TAS					I	HPO:iea[2015-05-03]
OMIM:601665	OBESITY		HP:0001513	OMIM:601665	TAS					P	HPO:iea[2009-02-17]
OMIM:601665	OBESITY		HP:0000006	OMIM:601665	TAS					I	HPO:skoehler[2015-12-30]
OMIM:228000	Farber lipogranulomatosis		HP:0003676	PMID:26945816	PCS					C	HPO:skoehler[2013-09-10];HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0010729	OMIM:228000	IEA					P	HPO:skoehler[2009-02-17]
OMIM:228000	Farber lipogranulomatosis		HP:0002240	PMID:30029679	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001270	OMIM:228000	IEA					P	HPO:iea[2009-02-17]
OMIM:228000	Farber lipogranulomatosis		HP:0010501	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001508	OMIM:228000	IEA					P	HPO:iea[2009-02-17]
OMIM:228000	Farber lipogranulomatosis		HP:0000737	OMIM:228000	IEA					P	HPO:iea[2009-02-17]
OMIM:228000	Farber lipogranulomatosis		HP:0011463	PMID:26945816	PCS		1/1			C	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001609	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0040139	OMIM:228000	IEA					P	HPO:skoehler[2015-01-21]
OMIM:228000	Farber lipogranulomatosis		HP:0001249	OMIM:228000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:228000	Farber lipogranulomatosis		HP:0001744	PMID:30029679	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001369	PMID:30029679	PCS					P	HPO:skoehler[2013-09-10];HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001386	PMID:26945816	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001187	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0003049	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001482	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0002093	OMIM:228000	IEA					P	HPO:iea[2009-02-17]
OMIM:228000	Farber lipogranulomatosis		HP:0007470	PMID:26945816	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0034053	PMID:30029679	PCS					P	HPO:probinson[2022-02-03]
OMIM:228000	Farber lipogranulomatosis		HP:0002829	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0009771	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0009134	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0000007	PMID:8955159	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001954	PMID:26945816	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:228000	Farber lipogranulomatosis		HP:0001615	OMIM:228000	IEA					P	HPO:iea[2009-02-17]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0001771	PMID:37919452	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0003233	PMID:37919452	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0004322	PMID:37919452	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002064	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0003593	PMID:37919452	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0003074	PMID:37919452	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0011463	PMID:37919452	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0011462	PMID:37919452	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000956	PMID:37919452	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0003307	PMID:37919452	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002857	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0040217	PMID:37919452	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0001249	PMID:37919452	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000831	PMID:37919452	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0001007	PMID:37919452	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002155	PMID:37919452	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000771	PMID:37919452	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002076	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000490	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0001263	PMID:37919452	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0004691	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0100578	PMID:37919452	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002829	PMID:37919452	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000448	PMID:37919452	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000007	PMID:37919452	PCS					I	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0003712	PMID:37919452	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000444	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000369	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000842	PMID:37919452	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0001397	PMID:37919452	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002240	PMID:37919452	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0033794	PMID:37919452	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0009125	PMID:37919452	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0007108	PMID:37919452	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0003326	PMID:37919452	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0003621	PMID:37919452	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002650	PMID:37919452	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0001761	PMID:37919452	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0001284	PMID:37919452	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000470	PMID:37919452	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000826	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0002808	PMID:37919452	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0007099	PMID:37919452	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000822	PMID:37919452	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000821	PMID:37919452	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0030051	PMID:37919452	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000147	PMID:37919452	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0000303	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:620683	Lipodystrophy, familial partial, type 9		HP:0004425	PMID:37919452	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-08-13]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000286	PMID:25817016;PMID:35047859;PMID:26924530	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000164	PMID:26924530	PCS					P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000365	PMID:25817016;PMID:35047859;PMID:26924530	PCS		6/12			P	HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0004322	PMID:25817016;PMID:35047859;PMID:26924530	PCS		5/20			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0001250	PMID:25817016;PMID:35047859	PCS		2/10			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0003196	PMID:25817014;PMID:25817016;PMID:35047859;PMID:26924530	PCS		15/15			P	HPO:probinson[2022-09-05];HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0005450	PMID:25817014;PMID:26924530	PCS		4/4			P	HPO:probinson[2022-09-05];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0033725	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0010292	PMID:25817016;PMID:35047859;PMID:26924530	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0010297	PMID:25817016;PMID:35047859	PCS		7/11			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0010055	PMID:25817016;PMID:35047859	PCS		9/11			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0011461	PMID:25817016	PCS		1/8			C	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000316	PMID:35137569;PMID:25817014;PMID:25817016;PMID:35047859;PMID:26924530	PCS		15/16			P	HPO:probinson[2022-09-05];HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000678	OMIM:616331	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0009944	PMID:25817014	PCS		2/3			P	HPO:probinson[2022-09-05]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000677	PMID:25817014	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002751	PMID:26924530	PCS		4/9			P	HPO:probinson[2020-08-03]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000175	PMID:25817014;PMID:35047859	PCS		3/6			P	HPO:probinson[2022-09-05];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000054	PMID:25817016;PMID:35047859;PMID:26924530	PCS		6/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002870	PMID:25817016;PMID:35047859	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0001263	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0011800	PMID:25817014;PMID:25817016;PMID:35047859	PCS		14/14			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0012385	PMID:25817014;PMID:25817016;PMID:35047859	PCS		4/12			P	HPO:probinson[2022-09-05];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000407	PMID:25817014;PMID:25817016;PMID:35047859;PMID:26924530	PCS		3/12			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002827	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0001537	PMID:25817016;PMID:35047859	PCS		4/10			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000689	OMIM:616331	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000527	PMID:25817016;PMID:35047859	PCS		5/10			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0001539	PMID:25817016;PMID:35047859	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0009611	PMID:25817014;PMID:26924530	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000405	PMID:25817014;PMID:25817016;PMID:35047859;PMID:26924530	PCS		4/12			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000207	PMID:25817016;PMID:35047859	PCS		10/10			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000047	PMID:25817016;PMID:35047859;PMID:26924530	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000520	PMID:25817016;PMID:35047859;PMID:26924530	PCS		7/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000960	PMID:25817016;PMID:35047859;PMID:26924530	PCS		2/8			P	HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000006	PMID:25817016;PMID:26924530	PCS		20/20			I	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002984	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000369	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0003577	PMID:35137569;PMID:25817016;OMIM:616331;PMID:26924530	PCS		19/20			C	HPO:skoehler[2015-12-30];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000582	PMID:25817016;PMID:35047859;PMID:26924530	PCS		3/11			P	HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000343	PMID:25817016;OMIM:616331;PMID:35047859	PCS		17/21			P	ORCID:0000-0002-0736-9199[2024-10-31];HPO:skoehler[2015-05-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000463	PMID:25817016;PMID:35047859;PMID:26924530	PCS		10/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0001156	PMID:25817014;PMID:25817016;PMID:35047859;PMID:26924530	PCS		13/15			P	HPO:probinson[2022-09-05];HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000023	PMID:25817016;PMID:35047859	PCS		0/9			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002684	PMID:26924530	PCS		7/9			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002164	PMID:25817016;PMID:35047859	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000185	PMID:25817016;PMID:26924530	PCS		2/8			P	HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002240	PMID:35047859	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000060	PMID:25817016;PMID:35047859	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0003093	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0011994	PMID:25817016;PMID:35047859	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0001629	PMID:25817016;PMID:35047859	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0009882	OMIM:616331	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000219	PMID:35137569;PMID:25817016;PMID:35047859	PCS		5/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0030084	PMID:25817016;PMID:35047859;PMID:26924530	PCS		10/12			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000218	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000212	PMID:25817014;PMID:25817016;PMID:35047859;PMID:26924530	PCS		13/15			P	HPO:probinson[2022-09-05];HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000256	PMID:25817016;PMID:35047859;PMID:26924530	PCS		18/18			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000410	PMID:25817014	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000215	PMID:35137569	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000154	PMID:25817014	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0003027	PMID:25817014;PMID:25817016;PMID:35047859;PMID:26924530	PCS		10/15			P	HPO:probinson[2022-09-05];HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002650	PMID:25817016;PMID:35047859;PMID:26924530	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000431	PMID:25817016;PMID:35047859	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000592	PMID:25817016;PMID:35047859;PMID:26924530	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000470	PMID:25817016;PMID:35047859;PMID:26924530	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0005280	PMID:35137569;PMID:25817016;PMID:26924530	PCS		9/9			P	HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0011304	PMID:25817016;OMIM:616331;PMID:35047859	PCS		15/21			P	ORCID:0000-0002-0736-9199[2024-10-31];HPO:skoehler[2015-05-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000348	PMID:35137569;PMID:25817016;OMIM:616331;PMID:35047859;PMID:26924530	PCS		23/23			P	ORCID:0000-0002-0736-9199[2024-10-31];HPO:skoehler[2015-05-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0002007	PMID:25817016;PMID:35047859;PMID:26924530	PCS		11/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0009999	PMID:26924530	PCS		4/9			P	HPO:probinson[2020-08-03]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000028	PMID:25817016;PMID:35047859;PMID:26924530	PCS		5/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2024-10-31];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:616331	Robinow syndrome, autosomal dominant 2		HP:0000347	PMID:25817016;PMID:35047859;PMID:26924530	PCS		5/12			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-03];ORCID:0000-0002-0736-9199[2024-10-31]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0008936	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000297	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000494	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0001156	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0002032	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0001250	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000490	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000185	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0011304	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000319	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000568	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000659	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0001631	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000006	OMIM:614526	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0001249	OMIM:614526	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000501	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000347	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614526	Chromosome 17Q12 duplication syndrome		HP:0000325	OMIM:614526	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612631	Adenylate kinase deficiency, hemolytic anemia due to		HP:0001878	OMIM:612631	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612631	Adenylate kinase deficiency, hemolytic anemia due to		HP:0000007	OMIM:612631	TAS					I	HPO:skoehler[2012-10-17]
OMIM:612631	Adenylate kinase deficiency, hemolytic anemia due to		HP:6000558	PMID:7947281	PCS		6/6			P	HPO:probinson[2024-04-03]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0009053	PMID:21576112	PCS		11/15			P	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0008959	PMID:21576112	PCS		10/15			P	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0011463	PMID:21576112	PCS		2/15			C	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0000608	PMID:21576112	PCS		3/14			P	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0003581	PMID:21576112	PCS		13/15			C	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0002936	PMID:21576112	PCS		14/14			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0007149	PMID:21576112	PCS		10/15			P	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0000006	PMID:21576112	PCS					I	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0000974	PMID:21576112	PCS		4/14			P	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0008944	PMID:21576112	PCS		11/15			P	HPO:probinson[2022-05-29]
OMIM:619764	Charcot-Marie-Tooth disease, demyelinating, type 1H		HP:0006844	PMID:21576112	PCS		6/15			P	HPO:probinson[2022-05-29]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0002465	PMID:28007989	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0003676	PMID:28007989	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001250	PMID:28007989	PCS		5/5			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001252	PMID:25678555	PCS		1/1			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0002283	PMID:28007989	PCS		1/5			P	HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0003593	PMID:28007989;PMID:25678555	PCS		2/6			C	HPO:probinson[2023-05-08];HPO:skoehler[2015-12-30];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0012345	PMID:25678555	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001508	PMID:25678555	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001947	PMID:25678555	PCS		1/1			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001903	PMID:28007989	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0011463	PMID:28007989	PCS		4/5			C	HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001927	PMID:25678555	PCS		1/1			P	HPO:skoehler[2015-08-02]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001987	PMID:25678555	PCS		1/1		HP:0012825	P	HPO:skoehler[2015-08-02];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0002014	PMID:25678555	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0002136	PMID:25678555	PCS		1/1			P	HPO:skoehler[2015-08-02]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0002015	PMID:28007989	PCS		3/4			P	HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0002133	PMID:28007989	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001981	PMID:25678555	PCS		1/1			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0002376	PMID:28007989	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0001263	PMID:28007989;PMID:25678555	PCS		6/6			P	HPO:probinson[2023-05-08];HPO:skoehler[2015-08-02]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0003819	PMID:28007989	PCS		2/5			C	HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0000007	PMID:25678555	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0200134	PMID:28007989	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0004823	PMID:28007989;PMID:25678555	PCS		6/6			P	HPO:probinson[2023-05-08];HPO:skoehler[2015-08-02]
OMIM:616457	Developmental and epileptic encephalopathy 50		HP:0003218	PMID:28007989	PCS		0/5			P	HPO:probinson[2023-05-08]
OMIM:213900	Cerebral sclerosis similar to pelizaeus-merzbacher disease		HP:0000707	OMIM:213900	IEA					P	HPO:iea[2009-02-17]
OMIM:213900	Cerebral sclerosis similar to pelizaeus-merzbacher disease		HP:0001939	OMIM:213900	IEA					P	HPO:iea[2009-02-17]
OMIM:213900	Cerebral sclerosis similar to pelizaeus-merzbacher disease		HP:0000007	OMIM:213900	IEA					I	HPO:iea[2009-02-17]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000286	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000582	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000343	PMID:27900362	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000486	PMID:27900362	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000463	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000540	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0003196	PMID:27900362	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0001252	PMID:27900362	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0003593	OMIM:617991	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000639	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000957	OMIM:617991	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000718	PMID:27900362	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000739	PMID:27900362	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000316	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0008751	PMID:27900362	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000218	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000311	PMID:27900362	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0001249	PMID:27900362	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0009748	PMID:27900362	PCS		2/3			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0001385	PMID:27900362	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000574	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000233	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0001382	OMIM:617991	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0011968	PMID:27900362	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000490	PMID:27900362	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0001263	PMID:27900362	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0001182	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0100710	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0012420	PMID:27900362	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000348	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0004209	PMID:27900362	PCS		1/3			P	HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000400	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000664	OMIM:617991	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0007018	PMID:27900362	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000322	PMID:27900362	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000006	PMID:23033978	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000028	OMIM:617991	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0000347	PMID:27900362	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-21]
OMIM:617991	Developmental delay, intellectual disability, obesity, and dysmorphic features		HP:0001513	PMID:27900362	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-21]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000483	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000164	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002023	PMID:26833328	PCS		9/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000365	PMID:26833328	PCS		11/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000486	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001773	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0004322	PMID:26833328	PCS					P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001250	PMID:26833328	PCS		4/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001290	PMID:26833328	PCS		8/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0012745	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000518	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000319	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0011220	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000998	PMID:26833328	PCS		5/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001643	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002536	PMID:26833328	PCS		5/10			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001249	PMID:26833328	PCS					P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000358	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000175	PMID:26833328	PCS					P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001385	PMID:26833328	PCS		8/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000453	PMID:26833328	PCS		6/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002079	PMID:26833328	PCS		8/13			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0011968	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001382	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001263	PMID:26833328	PCS		17/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0012813	PMID:26833328	PCS		5/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001182	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0100259	PMID:26833328	PCS		9/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002827	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000448	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000601	PMID:26833328	PCS					P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000960	PMID:26833328	PCS		5/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000369	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000248	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000126	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000324	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000341	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000343	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000540	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001305	PMID:26833328	PCS		5/13			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000414	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002119	PMID:26833328	PCS		8/11			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001423	PMID:26833328	PCS					I	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000110	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002650	PMID:26833328	PCS		11/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000431	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000750	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001321	PMID:26833328	PCS		6/11			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001761	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002098	OMIM:300968	TAS	HP:0003623				P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000193	PMID:26833328	PCS		5/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0005280	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002926	PMID:26833328	PCS		6/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0100559	PMID:26833328	PCS		7/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0002205	PMID:26833328	PCS		9/17			P	HPO:probinson[2017-06-23]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0200055	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0001631	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300968	Intellectual developmental disorder, X-linked 99, syndromic, female-restricted		HP:0000545	OMIM:300968	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617985	Microcephaly 23, primary, autosomal recessive		HP:0000340	PMID:27737959	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-26]
OMIM:617985	Microcephaly 23, primary, autosomal recessive		HP:0000252	PMID:27737959	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-26]
OMIM:617985	Microcephaly 23, primary, autosomal recessive		HP:0003577	PMID:27737959	PCS		1/1			C	HPO:probinson[2022-03-26]
OMIM:617985	Microcephaly 23, primary, autosomal recessive		HP:0001518	PMID:27737959	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:617985	Microcephaly 23, primary, autosomal recessive		HP:0000007	PMID:27737959	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-26]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002487	OMIM:614254	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0003577	PMID:25864721	PCS		1/4			C	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002540	PMID:25864721	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001332	OMIM:614254	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001250	OMIM:614254	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002384	PMID:25864721;PMID:21376300	PCS		2/6			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001272	PMID:25864721	PCS		1/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0006829	OMIM:614254	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001252	PMID:21376300	PCS		1/2			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0003593	PMID:25864721	PCS		3/4			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0032794	PMID:25864721	PCS		1/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0100704	OMIM:614254	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002119	PMID:25864721	PCS		3/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0012171	PMID:25864721	PCS		2/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002019	OMIM:614254	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001249	PMID:21376300	PCS		2/2			P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001347	PMID:25864721	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0003763	PMID:25864721	PCS		1/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002059	PMID:25864721	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0000252	PMID:25864721	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001344	PMID:25864721	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002353	OMIM:614254	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002650	OMIM:614254	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002870	PMID:25864721	PCS		1/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002079	PMID:25864721	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0000276	PMID:25864721	PCS		3/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0011968	PMID:25864721	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0000490	PMID:25864721	PCS		3/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002072	PMID:25864721	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0010553	PMID:25864721	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0100660	PMID:25864721	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0011097	PMID:25864721	PCS		1/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0000748	PMID:25864721	PCS		2/4			P	HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0100716	OMIM:614254	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001257	OMIM:614254	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0000006	PMID:21376300	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-01-17]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0002126	OMIM:614254	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:614254	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant		HP:0001336	PMID:25864721	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-17]
OMIM:313900	Thrombocytopenia 1		HP:0003212	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:313900	Thrombocytopenia 1		HP:0003011	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:313900	Thrombocytopenia 1		HP:0001419	PMID:7795648	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:313900	Thrombocytopenia 1		HP:0001905	PMID:7795648	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:313900	Thrombocytopenia 1		HP:0000964	OMIM:313900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:313900	Thrombocytopenia 1		HP:0003261	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:313900	Thrombocytopenia 1		HP:0000967	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:313900	Thrombocytopenia 1		HP:0000978	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:313900	Thrombocytopenia 1		HP:0005261	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:313900	Thrombocytopenia 1		HP:0000421	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:313900	Thrombocytopenia 1		HP:0005537	PMID:7795648	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:313900	Thrombocytopenia 1		HP:0004854	OMIM:313900	IEA					P	HPO:iea[2009-02-17]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000286	PMID:19764024	PCS		1/3			P	HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000252	PMID:19764024	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000582	PMID:19764024	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0002650	PMID:19764024	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000431	PMID:19764024	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0001773	PMID:19764024	PCS		1/3			P	HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0004322	PMID:19764024	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000430	PMID:19764024	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0011968	PMID:19764024	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0001252	PMID:19764024	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0011971	PMID:19764024	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0009183	PMID:19764024	PCS		1/3			P	HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0011463	PMID:19764024	PCS					C	HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0008551	PMID:19764024	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000007	PMID:19764024	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000405	PMID:19764024	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000218	PMID:19764024	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0004209	PMID:19764024	PCS		2/3			P	HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0001249	PMID:19764024	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0000347	PMID:19764024	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-10-20]
OMIM:248910	Cutaneous mastocytosis, conductive hearing loss, and microtia		HP:0200151	PMID:19764024	PCS		3/3			P	HPO:skoehler[2013-06-16];HPO:probinson[2020-10-20]
OMIM:272440	Filippi syndrome		HP:0004325	OMIM:272440	TAS					P	HPO:skoehler[2012-11-16]
OMIM:272440	Filippi syndrome		HP:0001332	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0001272	OMIM:272440	TAS					P	HPO:skoehler[2012-11-16]
OMIM:272440	Filippi syndrome		HP:0001250	OMIM:272440	TAS					P	HPO:skoehler[2012-11-16]
OMIM:272440	Filippi syndrome		HP:0000062	OMIM:272440	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:272440	Filippi syndrome		HP:0011335	OMIM:272440	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272440	Filippi syndrome		HP:0012725	OMIM:272440	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272440	Filippi syndrome		HP:0008070	OMIM:272440	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:272440	Filippi syndrome		HP:0001629	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000954	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000998	OMIM:272440	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:272440	Filippi syndrome		HP:0000337	OMIM:272440	TAS					P	HPO:skoehler[2012-11-16]
OMIM:272440	Filippi syndrome		HP:0008897	OMIM:272440	PCS					P	HPO:probinson[2012-03-16]
OMIM:272440	Filippi syndrome		HP:0009765	OMIM:272440	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272440	Filippi syndrome		HP:0040019	OMIM:272440	IEA					P	HPO:skoehler[2018-10-08]
OMIM:272440	Filippi syndrome		HP:0001249	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000252	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000233	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000431	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000430	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0010714	OMIM:272440	PCS					P	HPO:probinson[2012-03-16]
OMIM:272440	Filippi syndrome		HP:0000691	OMIM:272440	TAS					P	HPO:skoehler[2015-02-22]
OMIM:272440	Filippi syndrome		HP:0006482	OMIM:272440	TAS					P	HPO:skoehler[2015-02-22]
OMIM:272440	Filippi syndrome		HP:0000668	OMIM:272440	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:272440	Filippi syndrome		HP:0000007	OMIM:272440	IEA					I	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000505	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000648	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0001511	OMIM:272440	PCS					P	HPO:probinson[2012-03-16]
OMIM:272440	Filippi syndrome		HP:0000322	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000520	OMIM:272440	IEA					P	HPO:iea[2009-02-17]
OMIM:272440	Filippi syndrome		HP:0000028	OMIM:272440	TAS					P	HPO:skoehler[2015-02-22]
OMIM:272440	Filippi syndrome		HP:0034270	PMID:25439729	PCS					P	HPO:probinson[2022-06-04]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0000486	PMID:32497488	PCS		4/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0025610	PMID:32497488	PCS		8/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0000491	PMID:32497488	PCS		4/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0001097	PMID:32497488	PCS		1/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0030318	PMID:32497488	PCS		2/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0008070	PMID:32497488	IEA		6/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0033194	PMID:32497488	PCS		2/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0031291	PMID:32497488	PCS		10/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0500262	PMID:32497488	PCS		5/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0000518	PMID:32497488	PCS		4/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0000613	PMID:32497488	PCS		10/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0008404	PMID:32497488	PCS		1/12			P	HPO:probinson[2020-12-03]
OMIM:619016	Ichthyosis, follicular, with atrichia and photophobia syndrome 2		HP:0000006	PMID:32497488	PCS					I	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:185070	Stormorken syndrome		HP:0001892	OMIM:185070	IEA					P	HPO:iea[2009-02-17]
OMIM:185070	Stormorken syndrome		HP:0003236	PMID:24619930	PCS		6/6			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0003676	OMIM:185070	TAS					C	HPO:skoehler[2017-07-13]
OMIM:185070	Stormorken syndrome		HP:0003750	OMIM:185070	IEA					P	HPO:iea[2009-02-17]
OMIM:185070	Stormorken syndrome		HP:0004322	OMIM:185070	TAS					P	HPO:skoehler[2017-07-13]
OMIM:185070	Stormorken syndrome		HP:0003198	OMIM:185070	TAS					P	HPO:skoehler[2014-08-03]
OMIM:185070	Stormorken syndrome		HP:0010522	OMIM:185070	IEA					P	HPO:skoehler[2010-06-18]
OMIM:185070	Stormorken syndrome		HP:0006270	PMID:24619930	PCS		2/6			P	HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0001903	PMID:24619930	PCS		6/6			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000616	PMID:24619930	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0001746	PMID:24619930	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000978	PMID:24619930	PCS		2/6			P	HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0025435	PMID:24619930	PCS		3/3			P	HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0003701	OMIM:185070	TAS					P	HPO:skoehler[2014-08-03]
OMIM:185070	Stormorken syndrome		HP:0003326	OMIM:185070	TAS					P	HPO:skoehler[2014-08-03]
OMIM:185070	Stormorken syndrome		HP:0002138	PMID:24619930	PCS		1/6			P	HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0002076	PMID:24619930	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000490	PMID:24619930	PCS		6/6			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000790	PMID:24619930	PCS		2/6			P	HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0008064	PMID:24619930	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0032550	OMIM:185070	IEA					P	HPO:skoehler[2019-09-07]
OMIM:185070	Stormorken syndrome		HP:0000448	PMID:24619930	PCS		6/6			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000601	PMID:24619930	PCS					P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000421	PMID:24619930	PCS		4/6			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0001873	PMID:24619930	PCS		5/6			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000322	PMID:24619930	PCS		2/6			P	HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0000006	PMID:24619930	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-02]
OMIM:185070	Stormorken syndrome		HP:0002401	PMID:24619930	PCS		3/3			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-04-02]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003577	PMID:20371544	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003473	PMID:15496425	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0001371	PMID:23326516	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0030210	PMID:15496425;PMID:20371544	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0001252	OMIM:616325	TAS	HP:0003623				P	HPO:skoehler[2015-05-31]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0001252	PMID:20371544	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003593	OMIM:616325	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0002380	PMID:23326516	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003391	PMID:23326516;PMID:19949040	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2015-05-31];HPO:probinson[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0030319	PMID:19949040;PMID:20371544	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0012473	PMID:23326516	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0011463	PMID:23326516;PMID:19949040	PCS		6/6			C	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003307	PMID:19949040	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0002515	PMID:23326516;PMID:19949040	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003327	PMID:23326516	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003547	PMID:19949040	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0008997	PMID:23326516;PMID:19949040;PMID:15496425;PMID:20371544	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003403	PMID:23326516;PMID:15496425;PMID:20371544	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003623	PMID:15496425	PCS		1/1			C	HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0025331	PMID:23326516;PMID:20371544	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0002015	PMID:23326516;PMID:15496425;PMID:20371544	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003324	PMID:15496425	PCS		1/1			P	HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0002650	PMID:23326516;PMID:20371544	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0003388	PMID:23326516;PMID:15496425;PMID:19949040	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2015-05-31];HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0002093	PMID:19949040;PMID:15496425;PMID:20371544	PCS		3/7		HP:0025303	P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2015-05-31]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0030208	PMID:23326516;PMID:15496425;PMID:20371544	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0010535	PMID:23326516	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0000508	PMID:23326516;PMID:19949040;PMID:15496425;PMID:20371544	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0000602	PMID:19949040;PMID:15496425	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2015-05-31]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0000007	PMID:15496425	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0001319	OMIM:616325	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0008944	PMID:23326516	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-08]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0001611	PMID:15496425;PMID:19949040;PMID:20371544	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:probinson[2023-03-22]
OMIM:616325	Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency		HP:0000467	OMIM:616325;PMID:19949040;PMID:15496425;PMID:20371544	PCS		13/17			P	ORCID:0000-0002-0736-9199[2024-05-08];HPO:skoehler[2015-05-31]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003697	OMIM:255160	IEA					P	HPO:iea[2009-02-17]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003236	PMID:17372140	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0004322	PMID:17372140	PCS		3/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0011712	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0033567	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0100306	PMID:17372140	PCS		3/3			P	HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0000218	PMID:17372140	PCS		1/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0025710	PMID:17372140	PCS		1/3			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0007126	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003704	OMIM:255160	IEA					P	HPO:iea[2009-02-17]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003803	OMIM:255160	IEA					P	HPO:iea[2009-02-17]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0001324	PMID:17372140	PCS					P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003701	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003325	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0001644	OMIM:255160	TAS					P	HPO:skoehler[2015-06-22]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0002875	PMID:17372140	PCS		2/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0002058	PMID:17372140	PCS		1/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003687	OMIM:255160	IEA					P	HPO:iea[2009-02-17]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0031659	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003621	PMID:17372140	PCS		1/3			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0002650	PMID:17372140	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0200128	PMID:17372140	PCS		2/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0030848	PMID:17372140	PCS		2/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0002093	OMIM:255160	TAS					P	HPO:skoehler[2015-06-22]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0011703	PMID:17372140	PCS		1/4			P	HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0002091	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0001639	PMID:17372140	PCS		3/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0008981	PMID:17372140	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0100613	PMID:17372140	PCS		1/3			C	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0000007	PMID:17372140	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0001635	PMID:17372140	PCS		2/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0002505	PMID:17372140	PCS	HP:0003596	1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0002943	PMID:17372140	PCS		3/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003677	PMID:17372140	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:255160	Myopathy, myosin storage, autosomal recessive		HP:0003458	PMID:17372140	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-08]
OMIM:619189	Li-Campeau syndrome		HP:0003577	PMID:33340455	PCS					C	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000343	PMID:33340455	PCS		2/7			P	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0004322	PMID:33340455	PCS		5/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001250	PMID:33340455	PCS		6/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001252	PMID:33340455	PCS		6/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001629	PMID:33340455	PCS	HP:0003577	2/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0011220	PMID:33340455	PCS		3/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000316	PMID:33340455	PCS		4/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000954	PMID:33340455	PCS		1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000998	PMID:33340455	PCS		1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001643	PMID:33340455	PCS	HP:0003623	2/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0002579	PMID:33340455	PCS		1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001249	PMID:33340455	PCS		7/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000054	PMID:33340455	PCS		1/6	MALE		P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000494	PMID:33340455	PCS		3/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000574	PMID:33340455	PCS		1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001263	PMID:33340455	PCS		7/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0003065	PMID:33340455	PCS		1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0033258	PMID:33340455	PCS	HP:0011463	1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000506	PMID:33340455	PCS		1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000508	PMID:33340455	PCS		5/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000007	PMID:33340455	PCS					I	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000821	PMID:33340455	PCS		4/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001631	PMID:33340455	PCS		1/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000028	PMID:33340455	PCS		5/6	MALE		P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0000369	PMID:33340455	PCS		3/7			P	HPO:probinson[2021-04-30]
OMIM:619189	Li-Campeau syndrome		HP:0001655	PMID:33340455	PCS	HP:0003623	1/7			P	HPO:probinson[2021-04-30]
OMIM:311050	Optic atrophy 2		HP:0007083	OMIM:311050	TAS					P	HPO:probinson[2013-03-14]
OMIM:311050	Optic atrophy 2		HP:0003487	OMIM:311050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311050	Optic atrophy 2		HP:0001260	OMIM:311050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311050	Optic atrophy 2		HP:0002075	OMIM:311050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311050	Optic atrophy 2		HP:0000648	OMIM:311050	TAS					P	HPO:skoehler[2010-06-20]
OMIM:311050	Optic atrophy 2		HP:0001417	OMIM:311050	TAS					I	HPO:skoehler[2009-02-17]
OMIM:311050	Optic atrophy 2		HP:0003438	OMIM:311050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311050	Optic atrophy 2		HP:0001249	OMIM:311050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:311050	Optic atrophy 2		HP:0001337	OMIM:311050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0001562	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000110	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0003577	PMID:24439109	PCS		4/4			C	HPO:skoehler[2014-04-13];HPO:probinson[2022-07-09]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0010958	PMID:24439109	PCS		4/4			P	HPO:probinson[2022-07-09]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0002089	PMID:24439109	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-09]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0001762	PMID:24439109	PCS		3/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-07-09]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000093	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000316	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000822	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000007	PMID:24439109	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-07-09]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000813	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0002009	PMID:24439109	PCS		3/3			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-07-09]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0025700	PMID:24439109	PCS		4/4			P	HPO:probinson[2022-07-09]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000278	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000369	OMIM:191830	TAS					P	HPO:skoehler[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000786	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:191830	Renal hypodysplasia/aplasia 1		HP:0000148	OMIM:191830	IEA					P	HPO:iea[2009-02-17]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0000252	PMID:23255472;PMID:11228268	PCS		1/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0003079	PMID:11228268	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0000992	PMID:23255472;PMID:11228268	PCS		3/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0001761	OMIM:278780	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0001263	PMID:23255472;PMID:11228268	PCS		1/3			P	HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0001251	OMIM:278780	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0003593	PMID:11228268	PCS		1/1			C	HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0012469	PMID:11228268	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0000518	PMID:11228268	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0001518	PMID:11228268	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0000007	PMID:11228268	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0000568	PMID:23255472;PMID:11228268	PCS		1/3			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0001510	OMIM:278780	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0001257	OMIM:278780	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0001337	OMIM:278780	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:278780	Xeroderma pigmentosum, complementation group G		HP:0003623	PMID:23255472	PCS		2/2			C	HPO:probinson[2022-03-15]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003434	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003236	PMID:32042919	PCS		0/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003596	PMID:34777884;PMID:32042919	PCS		2/2			C	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002067	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001332	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002066	PMID:30838265	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003551	PMID:34777884	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002063	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002460	PMID:34777884	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0100295	PMID:34777884	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003390	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000716	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0011462	PMID:30838265	PCS		1/1			C	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000712	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0007641	OMIM:258450	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003701	PMID:34777884	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003548	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001488	PMID:34777884;PMID:32042919	PCS		2/2			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003700	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003546	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003202	PMID:30838265	PCS		0/1			P	HPO:probinson[2022-05-30];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001265	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002078	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003200	PMID:34777884;PMID:32042919	PCS		2/2			P	HPO:probinson[2022-05-30];HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001300	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0006858	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000651	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003487	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001260	PMID:30838265	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002070	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001618	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000407	PMID:32042919	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000007	PMID:11431686	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000648	OMIM:258450	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002747	OMIM:258450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000565	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003713	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001653	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003557	PMID:34777884;PMID:32042919	PCS		2/2			P	HPO:probinson[2022-05-30];HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0010628	PMID:30838265	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003376	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001272	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0030319	PMID:34777884	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002080	PMID:34777884	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003688	PMID:32042919	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003689	PMID:34777884	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002015	PMID:30838265	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002650	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001761	PMID:30838265	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000590	PMID:34777884;PMID:30838265;PMID:32042919	PCS		3/3			P	HPO:probinson[2022-05-30];HPO:skoehler[2010-06-18];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001284	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0008180	OMIM:258450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000869	PMID:30838265	PCS		1/1			P	HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000508	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0000505	OMIM:258450	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002922	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001638	OMIM:258450	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003737	PMID:30838265	PCS				HP:0012828	P	HPO:probinson[2012-07-15];HPO:probinson[2022-05-30]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0002403	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0006886	OMIM:258450	IEA					P	HPO:iea[2012-04-28]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0001634	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:258450	Progressive external ophthalmoplegia with mitochondrial DNA deletions,autosomal recessive		HP:0003458	OMIM:258450	IEA					P	HPO:iea[2009-02-17]
OMIM:618283	Visual impairment and progressive phthisis bulbi		HP:0003577	PMID:29771303	PCS		3/3			C	HPO:probinson[2022-09-26]
OMIM:618283	Visual impairment and progressive phthisis bulbi		HP:0000540	PMID:29771303	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-26]
OMIM:618283	Visual impairment and progressive phthisis bulbi		HP:0000508	PMID:29771303	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-26]
OMIM:618283	Visual impairment and progressive phthisis bulbi		HP:0000007	PMID:29771303	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-26]
OMIM:618283	Visual impairment and progressive phthisis bulbi		HP:0000667	PMID:29771303	PCS	HP:0011462	3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-26]
OMIM:618283	Visual impairment and progressive phthisis bulbi		HP:0007663	PMID:29771303	PCS	HP:0003577	3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-26]
OMIM:618283	Visual impairment and progressive phthisis bulbi		HP:0007720	PMID:29771303	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-26]
OMIM:166260	Gnathodiaphyseal dysplasia		HP:0003621	PMID:15124103	PCS					C	HPO:probinson[2022-11-10]
OMIM:166260	Gnathodiaphyseal dysplasia		HP:0000938	PMID:15124103	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:166260	Gnathodiaphyseal dysplasia		HP:0005045	OMIM:166260	IEA					P	HPO:iea[2009-02-17]
OMIM:166260	Gnathodiaphyseal dysplasia		HP:0006487	OMIM:166260	IEA					P	HPO:iea[2009-02-17]
OMIM:166260	Gnathodiaphyseal dysplasia		HP:0002659	PMID:15124103	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:166260	Gnathodiaphyseal dysplasia		HP:0000006	PMID:15124103	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-10]
OMIM:166260	Gnathodiaphyseal dysplasia		HP:0002754	OMIM:166260	IEA					P	HPO:skoehler[2019-09-07]
OMIM:215550	Circumvallate placenta syndrome		HP:0001561	OMIM:215550	IEA					P	HPO:iea[2009-02-17]
OMIM:215550	Circumvallate placenta syndrome		HP:0000924	OMIM:215550	IEA					P	HPO:iea[2009-02-17]
OMIM:215550	Circumvallate placenta syndrome		HP:0000007	OMIM:215550	IEA					I	HPO:iea[2009-02-17]
OMIM:215550	Circumvallate placenta syndrome		HP:0002093	OMIM:215550	IEA					P	HPO:iea[2009-02-17]
OMIM:215550	Circumvallate placenta syndrome		HP:0002170	OMIM:215550	IEA					P	HPO:iea[2009-02-17]
OMIM:215550	Circumvallate placenta syndrome		HP:0000951	OMIM:215550	IEA					P	HPO:iea[2009-02-17]
OMIM:614491	Pseudohypoaldosteronism, type IIB		HP:0002153	OMIM:614491	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614491	Pseudohypoaldosteronism, type IIB		HP:0008242	OMIM:614491	IEA					P	HPO:skoehler[2015-01-19]
OMIM:614491	Pseudohypoaldosteronism, type IIB		HP:0004918	OMIM:614491	TAS					P	HPO:probinson[2013-01-22]
OMIM:614491	Pseudohypoaldosteronism, type IIB		HP:0000822	OMIM:614491	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614491	Pseudohypoaldosteronism, type IIB		HP:0011423	OMIM:614491	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614491	Pseudohypoaldosteronism, type IIB		HP:0000006	OMIM:614491	TAS					I	HPO:skoehler[2012-10-17]
OMIM:615957	Spinocerebellar ataxia 38		HP:0003477	PMID:25065913	PCS		5/8			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0003596	PMID:25065913	PCS		4/9			C	HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0001260	PMID:25065913	PCS		6/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0002066	PMID:25065913	PCS		9/9			P	HPO:skoehler[2014-10-06]
OMIM:615957	Spinocerebellar ataxia 38		HP:0001251	PMID:25065913	PCS		9/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0002460	PMID:25065913	PCS		2/9			P	HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0002070	PMID:25065913	PCS		9/9			P	HPO:skoehler[2014-10-06]
OMIM:615957	Spinocerebellar ataxia 38		HP:0000639	PMID:25065913	PCS		8/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0011462	PMID:25065913	PCS		5/9			C	HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0000514	PMID:25065913	PCS		5/9			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0007366	PMID:25065913	PCS		0/7			P	HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0000006	PMID:25065913	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0003677	PMID:25065913	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0001337	PMID:25065913	PCS		1/9			P	HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0001336	PMID:25065913	PCS		0/9			P	HPO:probinson[2023-02-07]
OMIM:615957	Spinocerebellar ataxia 38		HP:0006855	PMID:25065913	PCS		7/7			P	HPO:probinson[2023-02-07]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:6000693	PMID:37913506	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0003596	PMID:37913506	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:6000691	PMID:37913506	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0031295	PMID:37913506	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0005110	PMID:37913506	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0000822	PMID:37913506	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0000007	PMID:37913506	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0004749	PMID:37913506	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0033534	PMID:37913506	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620734	Cardiomyopathy, familial hypertrophic, 30, atrial		HP:0012664	PMID:37913506	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0003202	OMIM:616286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0002059	OMIM:616286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001561	OMIM:616286	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0002079	OMIM:616286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001272	OMIM:616286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0005684	PMID:24319099	PCS		4/4			P	HPO:probinson[2023-02-23]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001252	OMIM:616286	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001284	OMIM:616286	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001290	OMIM:616286	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0003470	OMIM:616286	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0012697	OMIM:616286	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0006380	OMIM:616286	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0034197	PMID:24319099	PCS		4/4			C	HPO:probinson[2023-02-23]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0200136	OMIM:616286	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0000007	PMID:24319099	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-23]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001558	OMIM:616286	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001349	OMIM:616286	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0001989	PMID:24319099	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-23]
OMIM:616286	Lethal congenital contracture syndrome 7		HP:0000347	PMID:24319099	PCS		1/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-23]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0002267	PMID:15215304	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0001276	PMID:15215304	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0002069	PMID:21633362	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0003577	PMID:15215304	PCS		1/1			C	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0002376	PMID:15215304	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0000243	PMID:21633362	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0002384	PMID:21633362	PCS		1/2			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0001263	PMID:21633362;PMID:15215304	PCS		3/3			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0003593	PMID:21633362	PCS		1/2			C	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0003819	PMID:15215304	PCS		1/1			C	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0001419	PMID:15215304	PCS					I	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0011463	PMID:21633362	PCS		1/2			C	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0032792	PMID:15215304	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0001548	PMID:21633362	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0007333	PMID:21633362	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0200134	PMID:15215304	PCS		1/1			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-18]
OMIM:300607	Developmental and epileptic encephalopathy 8		HP:0006821	PMID:21633362	PCS		1/2			P	HPO:probinson[2023-02-18]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000286	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0007759	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000244	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000365	PMID:34513757;PMID:28446956	PCS		4/4			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0003355	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001250	PMID:34513757;PMID:28446956	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0010808	OMIM:214100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001252	PMID:33708531	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0003593	PMID:34513757	PCS		2/2			C	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001290	OMIM:214100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000518	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000639	PMID:28446956	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0012592	OMIM:214100	TAS					P	HPO:skoehler[2014-01-28]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000316	PMID:33708531	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000954	OMIM:214100;PMID:33708531	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000835	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002416	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001401	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000158	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001643	PMID:33708531	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001840	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000311	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000512	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000358	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0003623	PMID:33708531	PCS		1/1			C	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0005469	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001265	OMIM:214100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002750	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0011968	PMID:33708531	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001263	PMID:34513757;PMID:28446956	PCS		4/4			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0004492	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000407	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000007	PMID:9398848	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002705	OMIM:214100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002505	PMID:28446956	PCS		1/2			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000047	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000369	PMID:33708531	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000126	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0003455	PMID:34513757	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000582	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002089	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000463	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001591	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000260	PMID:33708531	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002120	PMID:28446956	PCS	HP:0003593	1/1			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002240	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000580	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0011039	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002282	OMIM:214100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001193	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0012368	OMIM:214100	TAS					P	HPO:skoehler[2013-10-22]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001508	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001629	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0009487	OMIM:214100	TAS					P	HPO:skoehler[2015-12-30]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0006894	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002317	PMID:34513757	PCS		1/2			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000218	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002359	PMID:34513757	PCS		1/2			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000256	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0005989	OMIM:214100	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001623	OMIM:214100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0006579	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0004734	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001088	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002015	PMID:34513757	PCS		1/2			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001762	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000750	PMID:34513757	PCS		2/2			P	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001284	OMIM:214100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000272	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0010655	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0007370	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0001838	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0003819	PMID:34513757	PCS		1/2			C	HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000348	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0008665	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002967	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000543	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000028	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000501	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0000347	PMID:33708531	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-12]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002126	OMIM:214100	IEA					P	HPO:iea[2009-02-17]
OMIM:214100	Peroxisome biogenesis disorder 1A (Zellweger)		HP:0002643	PMID:33708531	PCS		1/1			P	HPO:probinson[2022-03-12]
OMIM:601088	Ayme-Gripp syndrome		HP:0000164	PMID:30160832	PCS		6/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000582	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000343	PMID:30160832	PCS		11/15			P	HPO:probinson[2012-05-01];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000365	PMID:30160832	PCS		15/15			P	HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0001156	PMID:30160832	PCS		12/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0004322	OMIM:601088	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:601088	Ayme-Gripp syndrome		HP:0001250	PMID:30160832	PCS		8/10			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000160	PMID:30160832	PCS		10/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0004484	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0003196	PMID:30160832	PCS		13/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0012368	OMIM:601088	TAS					P	HPO:skoehler[2013-10-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000319	OMIM:601088	TAS					P	HPO:probinson[2012-05-01]
OMIM:601088	Ayme-Gripp syndrome		HP:0000519	PMID:30160832	PCS		14/15			P	HPO:iea[2009-02-17];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0008551	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000316	PMID:30160832	PCS		9/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0001701	PMID:30160832	PCS		6/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000219	PMID:30160832	PCS		10/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0001249	PMID:30160832	PCS		15/15			P	HPO:iea[2009-02-17];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000358	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0002974	OMIM:601088	IEA					P	HPO:iea[2009-02-17]
OMIM:601088	Ayme-Gripp syndrome		HP:0002059	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000494	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000431	OMIM:601088	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000270	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000272	OMIM:601088	IEA					P	HPO:iea[2009-02-17]
OMIM:601088	Ayme-Gripp syndrome		HP:0011800	PMID:30160832	PCS		15/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0001182	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0011229	PMID:30160832	PCS		8/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0005280	PMID:30160832	PCS		11/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0012385	PMID:30160832	PCS		HP:0040283			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000407	OMIM:601088	IEA					P	HPO:iea[2009-02-17]
OMIM:601088	Ayme-Gripp syndrome		HP:0007099	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000508	OMIM:601088	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0002209	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000767	PMID:30160832	PCS		3/15			P	HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000348	PMID:30160832	PCS		11/15			P	HPO:skoehler[2015-06-22];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0008404	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000289	OMIM:601088	TAS					P	HPO:probinson[2012-05-01]
OMIM:601088	Ayme-Gripp syndrome		HP:0000006	PMID:30160832	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-20]
OMIM:601088	Ayme-Gripp syndrome		HP:0000369	OMIM:601088	TAS					P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000303	OMIM:601088	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:601088	Ayme-Gripp syndrome		HP:0000248	OMIM:601088	IEA					P	HPO:skoehler[2019-02-22]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0000464	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001773	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0000486	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001310	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0004322	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001272	PMID:26437881	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002066	PMID:26437881	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002283	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001251	PMID:26437881	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0003593	PMID:26437881	PCS		2/2			C	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0000280	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002080	PMID:26437881	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0007063	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0007047	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001007	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001265	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002136	PMID:26437881	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0000750	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0004279	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002078	OMIM:610185	TAS					P	HPO:skoehler[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001321	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0031936	PMID:26437881	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002079	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001260	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001263	PMID:26437881	PCS		2/2			P	HPO:skoehler[2012-10-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002075	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0000407	PMID:26437881	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0000007	PMID:21885617	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0200055	OMIM:610185	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002942	OMIM:610185	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0002943	OMIM:610185	IEA					P	HPO:iea[2009-02-17]
OMIM:610185	Cerebellar ataxia, impaired intellectual development, and dysquilibrium syndrome 2		HP:0001337	OMIM:610185	IEA					P	HPO:skoehler[2010-06-18]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0010628	OMIM:310400	TAS					P	HPO:probinson[2012-04-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001371	OMIM:310400	TAS					P	HPO:probinson[2012-04-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0002021	OMIM:310400	IEA					P	HPO:iea[2009-02-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0006829	OMIM:310400	IEA					P	HPO:iea[2009-02-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001270	PMID:9931531	PCS					P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0011410	PMID:9931531	PCS		19/42			P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0030919	PMID:9931531	PCS		19/39			P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0030918	PMID:9931531	PCS		35/39			P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000238	OMIM:310400	IEA					P	HPO:iea[2009-02-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001305	PMID:9931531	PCS		1/45			P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000218	PMID:9931531	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000256	OMIM:310400	IEA					P	HPO:iea[2009-02-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0002910	PMID:9931531	PCS		6/45			P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001622	PMID:9931531	PCS		10/42			P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001166	PMID:9931531	PCS		9/21			P	HPO:probinson[2012-04-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000275	OMIM:310400	TAS					P	HPO:probinson[2012-05-01]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0003324	OMIM:310400	TAS					P	HPO:probinson[2012-04-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001561	PMID:9931531	PCS		14/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0002375	OMIM:310400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000276	PMID:9931531	PCS					P	HPO:probinson[2012-04-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0011308	OMIM:310400	TAS					P	HPO:probinson[2012-04-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001284	PMID:9931531	PCS		18/29			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0033454	PMID:9931531	PCS					P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0009110	OMIM:310400	IEA					P	HPO:iea[2009-02-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001419	PMID:8640223	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001558	PMID:9931531	PCS		21/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000348	PMID:9931531	PCS					P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000689	PMID:9931531	PCS					P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0001319	PMID:9931531	PCS	HP:0003577	45/45			P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0003517	PMID:9931531	PCS		25/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000268	PMID:9931531	PCS					P	HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000028	PMID:9931531	PCS		17/30			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0002643	PMID:9931531	PCS		33/41			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000544	OMIM:310400	IEA					P	HPO:iea[2009-02-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0000467	OMIM:310400	IEA					P	HPO:iea[2009-02-17]
OMIM:310400	Myopathy, centronuclear, X-linked		HP:0004887	OMIM:310400	IEA		28/35			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-28]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0008726	OMIM:202010	TAS					P	HPO:probinson[2012-06-10]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0000013	OMIM:202010	TAS					P	HPO:probinson[2012-06-10]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0004322	OMIM:202010	IEA					P	HPO:iea[2009-02-17]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0000040	PMID:2022736	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0000061	PMID:2022736	PCS		4/4	FEMALE		P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0003351	PMID:2022736	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0030088	PMID:2022736	PCS		7/7			P	HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0025380	PMID:2022736	PCS		7/7			P	HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0008185	PMID:2022736	PCS		5/7	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0000822	PMID:2022736	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0000007	PMID:2022736	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0000953	OMIM:202010	TAS					P	HPO:skoehler[2009-02-17]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0025436	PMID:2022736	PCS		7/7			P	HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0002900	OMIM:202010	IEA					P	HPO:iea[2009-02-17]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0008665	OMIM:202010	IEA					P	HPO:iea[2009-02-17]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0008258	OMIM:202010	IEA					P	HPO:iea[2009-02-17]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0004319	PMID:2022736	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0005616	OMIM:202010	IEA					P	HPO:iea[2009-02-17]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0000840	OMIM:202010	IEA					P	HPO:iea[2009-02-17]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0008734	PMID:2022736	PCS		5/7	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:202010	Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency		HP:0003623	OMIM:202010	IEA					C	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0001265	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003378	OMIM:605588	TAS					P	HPO:probinson[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0002751	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003376	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003431	OMIM:605588	PCS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0001761	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003693	PMID:11799477	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003484	OMIM:605588	IEA					P	HPO:probinson[2012-03-13]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003383	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0001284	PMID:11799477	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0002460	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003384	OMIM:605588	TAS					P	HPO:probinson[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003380	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0009027	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0000007	PMID:11799477	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0002936	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:605588	Charcot-Marie-Tooth disease, axonal, type 2B1		HP:0003701	OMIM:605588	IEA					P	HPO:iea[2009-02-17]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0003577	PMID:15955094	PCS		3/3			C	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0000343	PMID:15955094	PCS		1/4			P	HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0001058	PMID:9580666	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0000023	PMID:9580666;PMID:15955094	PCS		4/6			P	HPO:probinson[2022-07-02];HPO:iea[2009-02-17];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0002110	PMID:15955094	PCS		2/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0001582	PMID:9580666	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0002097	PMID:15955094	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0002094	PMID:15955094	PCS		1/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0001629	PMID:15955094	PCS		1/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0007495	PMID:15955094	PCS					P	HPO:probinson[2012-07-25];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0001635	PMID:15955094	PCS		1/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0000139	PMID:15955094	PCS		1/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0004969	PMID:9580666	PCS		1/1			P	HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0001659	OMIM:123700	TAS					P	HPO:iea[2009-02-17]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0000444	PMID:15955094	PCS		1/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0001653	OMIM:123700	TAS					P	HPO:iea[2009-02-17]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0000006	PMID:9580666	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0000974	PMID:9580666	PCS		0/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0005328	PMID:15955094	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-02]
OMIM:123700	Cutis laxa, autosomal dominant 1		HP:0000973	PMID:15955094	PCS		2/3			P	HPO:probinson[2022-07-02];HPO:probinson[2022-07-02]
OMIM:614485	Trigonocephaly 2		HP:0000252	PMID:21931569	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-05]
OMIM:614485	Trigonocephaly 2		HP:0000494	PMID:21931569	PCS		1/2			P	HPO:probinson[2023-03-05]
OMIM:614485	Trigonocephaly 2		HP:0000431	PMID:21931569	PCS		1/2			P	HPO:probinson[2023-03-05]
OMIM:614485	Trigonocephaly 2		HP:0000243	PMID:21931569	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614485	Trigonocephaly 2		HP:0011330	OMIM:614485	TAS					P	HPO:skoehler[2015-08-05]
OMIM:614485	Trigonocephaly 2		HP:0001263	PMID:21931569	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:614485	Trigonocephaly 2		HP:0000316	OMIM:614485	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614485	Trigonocephaly 2		HP:0005280	PMID:21931569	PCS		1/2			P	HPO:probinson[2023-03-05]
OMIM:614485	Trigonocephaly 2		HP:0000006	PMID:21931569	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:314100	Thumbs, congenital clasped		HP:0000924	OMIM:314100	IEA					P	HPO:iea[2009-02-17]
OMIM:314100	Thumbs, congenital clasped		HP:0001419	OMIM:314100	IEA					I	HPO:iea[2009-02-17]
OMIM:314100	Thumbs, congenital clasped		HP:0000707	OMIM:314100	IEA					P	HPO:iea[2009-02-17]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0003577	PMID:15596564	PCS		2/5			C	HPO:probinson[2022-07-10]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0034197	PMID:15596564	PCS		3/5			C	HPO:probinson[2022-07-10]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0031295	PMID:15596564	PCS		1/5			P	HPO:probinson[2022-07-10]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0005110	PMID:15596564	PCS		5/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-07-10]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0000007	PMID:19070573	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-10]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0004749	PMID:15596564	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-07-10]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0001645	PMID:15596564	PCS		2/5			P	HPO:probinson[2022-07-10]
OMIM:615770	Atrial fibrillation, familial, 15		HP:0004755	PMID:15596564	PCS		3/5			P	HPO:probinson[2022-07-10]
OMIM:616279	Cataract 43		HP:0007787	PMID:24549050	PCS	HP:0003621	9/9			P	HPO:probinson[2022-04-12]
OMIM:616279	Cataract 43		HP:0000006	PMID:24549050	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0005403	OMIM:601705	TAS					P	HPO:iea[2015-05-03]
OMIM:601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0001596	OMIM:601705	TAS	HP:0003577				P	HPO:skoehler[2010-06-20]
OMIM:601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0001807	OMIM:601705	TAS					P	HPO:iea[2015-05-03]
OMIM:601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0005352	OMIM:601705	TAS					P	HPO:iea[2009-02-17]
OMIM:601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0000007	OMIM:601705	TAS					I	HPO:iea[2009-02-17]
OMIM:601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0001803	OMIM:601705	TAS					P	HPO:iea[2015-05-03]
OMIM:601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0008404	OMIM:601705	IEA					P	HPO:skoehler[2015-12-30]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0031417	PMID:30388400	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0003577	PMID:30388400	PCS					C	HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0006528	PMID:30388400	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0001651	PMID:30388400	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0002783	PMID:30388400	PCS		2/2			P	HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0002110	PMID:30388400	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0001719	PMID:30388400	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0033036	PMID:30388400	PCS		1/1			P	HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0000007	PMID:30388400	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0012735	PMID:30388400	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-25]
OMIM:618254	Ciliary dyskinesia, primary, 39		HP:0000403	PMID:30388400	PCS		2/2			P	HPO:probinson[2021-02-25]
OMIM:136480	Fourth cranial nerve palsy, familial congenital		HP:0025592	OMIM:136480	IEA					P	HPO:skoehler[2018-10-08]
OMIM:136480	Fourth cranial nerve palsy, familial congenital		HP:0007011	OMIM:136480	IEA					P	HPO:iea[2009-02-17]
OMIM:136480	Fourth cranial nerve palsy, familial congenital		HP:0025404	PMID:3985833	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:136480	Fourth cranial nerve palsy, familial congenital		HP:0000542	PMID:3985833	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:136480	Fourth cranial nerve palsy, familial congenital		HP:0000006	OMIM:136480	IEA					I	HPO:iea[2009-02-17]
OMIM:136480	Fourth cranial nerve palsy, familial congenital		HP:0011514	PMID:3985833	PCS					P	HPO:lccarmody[2018-10-02]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0001344	PMID:28669405	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0000750	PMID:28669405	PCS		4/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0001250	PMID:28669405	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0002384	PMID:28669405	PCS		1/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0001263	PMID:28669405	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0001252	PMID:28669405	PCS		4/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0003593	PMID:28669405	PCS		1/2			C	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0033454	PMID:28669405	PCS		1/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0012444	PMID:28669405	PCS		1/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0012469	PMID:28669405	PCS		1/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0011463	PMID:28669405	PCS		1/2			C	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0032792	PMID:28669405	PCS		1/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0200134	PMID:28669405	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0002317	PMID:28669405	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0025116	PMID:28669405	PCS		1/4			P	HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0001249	PMID:28669405	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-12]
OMIM:617601	Intellectual developmental disorder, autosomal dominant 46		HP:0000006	PMID:28669405	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-12]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0003202	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0003676	OMIM:112250	TAS					C	HPO:skoehler[2012-10-17]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0005686	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0003198	OMIM:112250	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0007819	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0005045	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0005010	OMIM:112250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0003084	OMIM:112250	TAS					P	HPO:skoehler[2012-11-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0003690	OMIM:112250	TAS	HP:0003584				P	HPO:skoehler[2012-11-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0031367	OMIM:112250	IEA					P	HPO:skoehler[2018-10-08]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0100244	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0100254	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0012315	OMIM:112250	IEA					P	HPO:skoehler[2015-01-21]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0000938	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0002979	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0002669	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0000978	OMIM:112250	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0000977	OMIM:112250	TAS		HP:0040283			P	HPO:skoehler[2013-08-07]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0003701	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0002216	OMIM:112250	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0002756	OMIM:112250	TAS					P	HPO:probinson[2012-07-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0000006	OMIM:112250	TAS					I	HPO:probinson[2009-02-17]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0000963	OMIM:112250	TAS		HP:0040283			P	HPO:skoehler[2012-11-16]
OMIM:112250	Diaphyseal medullary stenosis with malignant fibrous histiocytoma		HP:0003325	OMIM:112250	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300834	Macular degeneration, X-linked atrophic		HP:0001419	PMID:12160730	PCS					I	HPO:probinson[2013-01-09]
OMIM:300834	Macular degeneration, X-linked atrophic		HP:0000608	PMID:12160730	PCS					P	HPO:probinson[2013-02-19]
OMIM:300834	Macular degeneration, X-linked atrophic		HP:0007663	PMID:12160730	PCS					P	HPO:probinson[2013-02-19]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0003621	PMID:34782440	PCS		1/3			C	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0008905	PMID:34782440	PCS		3/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0002980	PMID:34782440	PCS		1/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0002750	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0011968	PMID:34782440	PCS		1/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0001252	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0000592	PMID:34782440	PCS		1/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0003593	PMID:34782440	PCS		1/3			C	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0010047	PMID:34782440	PCS		1/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0011304	PMID:34782440	PCS		2/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0011463	PMID:34782440	PCS		1/3			C	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0010044	PMID:34782440	PCS		1/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0000926	PMID:34782440	PCS		3/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0000007	PMID:34782440	PCS					I	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0002942	PMID:34782440	PCS		2/3			P	HPO:probinson[2022-02-02];HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0002645	PMID:34782440	PCS		1/1			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0001763	PMID:34782440	PCS		1/2			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0000325	PMID:34782440	PCS		1/3			P	HPO:probinson[2022-02-02]
OMIM:619638	Spondylometaphyseal dysplasia, Pagnamenta type		HP:0002753	PMID:34782440	PCS		1/3			P	HPO:probinson[2022-02-02]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0000750	PMID:27523599	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0001662	PMID:27523599	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0011704	PMID:27523599	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0001250	PMID:27523599	PCS		4/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0001263	PMID:27523599	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0001252	PMID:27523599	PCS		6/9			P	HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0002020	PMID:27523599	PCS		5/8			P	HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0003593	PMID:27523599	PCS					C	HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0000639	PMID:27523599	PCS		6/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0000546	PMID:27523599	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0000007	PMID:27523599	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0000512	PMID:27523599	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:617173	Intellectual developmental disorder with cardiac arrhythmia		HP:0001249	PMID:27523599	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-06]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0001276	PMID:19463981	PCS		3/5			P	HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0011968	PMID:19463981	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0000260	PMID:19463981	PCS		1/5			P	HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0000072	PMID:19463981	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0001263	PMID:19463981	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0003593	PMID:19463981	PCS		1/5			C	HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0002490	PMID:19463981	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0032794	PMID:19463981	PCS		1/5			P	HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0011923	PMID:19463981	PCS		5/5			P	HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0000817	PMID:19463981	PCS		1/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0000007	PMID:19463981	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0002878	PMID:19463981	PCS		2/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0001522	PMID:19463981	PCS		5/5			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0000543	PMID:19463981	PCS		1/1			P	HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0000256	PMID:19463981	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0000126	PMID:19463981	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0001347	PMID:19463981	PCS		1/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0003128	PMID:19463981	PCS		4/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0001336	PMID:19463981	PCS		1/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-24]
OMIM:618240	Mitochondrial complex I deficiency, nuclear type 18		HP:0003623	PMID:19463981	PCS		4/5			C	HPO:probinson[2022-11-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0003577	PMID:18711368	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0001332	PMID:18711368	PCS		31/34			P	HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0001250	OMIM:277470	IEA					P	HPO:iea[2009-02-17]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002120	OMIM:277470	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0012110	OMIM:277470	TAS					P	HPO:probinson[2014-04-22]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0000711	OMIM:277470	TAS	HP:0003577				P	HPO:skoehler[2012-11-26]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0008872	OMIM:277470	IEA					P	HPO:iea[2009-02-17]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002518	OMIM:277470	TAS					P	HPO:skoehler[2013-06-05]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0000253	PMID:18711368	PCS		33/33			P	HPO:skoehler[2013-01-22];HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002179	OMIM:277470	IEA					P	HPO:iea[2009-02-17]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0000252	PMID:18711368	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0007308	OMIM:277470	IEA					P	HPO:iea[2009-02-17]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002015	PMID:18711368	PCS		30/32			P	HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0001561	PMID:18711368	PCS		0/34			P	HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0001321	PMID:18711368	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002033	OMIM:277470	TAS					P	HPO:skoehler[2012-11-26]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002171	OMIM:277470	TAS					P	HPO:skoehler[2012-11-26]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002072	PMID:18711368	PCS		31/34			P	HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0011344	OMIM:277470	TAS					P	HPO:probinson[2009-02-17]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0003819	OMIM:277470	TAS		HP:0040283			C	HPO:skoehler[2012-11-26]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0007772	OMIM:277470	IEA					P	HPO:iea[2009-02-17]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002803	PMID:18711368	PCS		0/34			P	HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0000007	PMID:18711368	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0000505	PMID:18711368	PCS		30/32			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0000648	PMID:18711368	PCS		0/25			P	HPO:probinson[2022-09-24]
OMIM:277470	Pontocerebellar hypoplasia, type 2A		HP:0002500	OMIM:277470	TAS					P	HPO:skoehler[2012-11-26]
OMIM:619176	Oocyte maturation defect 10		HP:0005268	PMID:31704776	PCS		1/2			C	HPO:probinson[2021-04-30]
OMIM:619176	Oocyte maturation defect 10		HP:0008222	PMID:31704776	PCS		2/2			P	HPO:probinson[2021-04-03]
OMIM:619176	Oocyte maturation defect 10		HP:0003581	PMID:31704776	PCS					C	HPO:probinson[2021-04-30];HPO:probinson[2021-04-30]
OMIM:619176	Oocyte maturation defect 10		HP:0000007	PMID:31704776	PCS					I	HPO:probinson[2021-04-03];HPO:probinson[2021-04-03]
OMIM:619176	Oocyte maturation defect 10		HP:0033712	PMID:31704776	PCS		2/2			P	HPO:probinson[2021-04-30]
OMIM:619176	Oocyte maturation defect 10		HP:4000008	PMID:31704776	PCS		2/2			P	HPO:probinson[2021-04-30]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0003577	PMID:10788335	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0001250	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:6000576	PMID:10788335	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000581	OMIM:606056	IEA					P	HPO:iea[2009-02-17]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0001252	OMIM:606056	IEA					P	HPO:iea[2009-02-17]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0002240	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0001290	PMID:10788335	PCS	HP:0003577	1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0012745	PMID:10788335	PCS		1/1			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0008872	OMIM:606056	IEA					P	HPO:iea[2009-02-17]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0002757	OMIM:606056	TAS					P	HPO:skoehler[2014-10-06]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000218	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000278	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0007108	PMID:10788335	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0001188	PMID:10788335;OMIM:606056	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0002059	OMIM:606056	TAS					P	HPO:skoehler[2014-10-06]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0004313	OMIM:606056	TAS					P	HPO:skoehler[2014-10-06]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0031956	PMID:10788335	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0002079	OMIM:606056	TAS					P	HPO:skoehler[2014-10-06]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0002791	OMIM:606056	IEA					P	HPO:iea[2009-02-17]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0012815	PMID:10788335	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0001263	OMIM:606056	TAS					P	HPO:skoehler[2014-10-06]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0010851	PMID:10788335	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0010557	PMID:10788335	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000407	OMIM:606056	TAS					P	HPO:skoehler[2014-10-06]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0007430	PMID:10788335	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000007	PMID:10788335	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000527	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000648	OMIM:606056	TAS					P	HPO:skoehler[2014-10-06]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0002943	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0002720	PMID:10788335	PCS		1/1			P	HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000269	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:606056	Congenital disorder of glycosylation, type IIB		HP:0000445	PMID:10788335	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0004325	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000286	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000483	PMID:30401460	PCS		1/3			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002224	PMID:30401460	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001410	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001773	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001250	PMID:30401460	PCS		1/3			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0003155	PMID:30401460	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001252	PMID:30401460	PCS		4/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002020	PMID:30401460	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000280	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0033725	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0012471	PMID:30401460	PCS		4/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000316	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001845	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000678	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000158	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001643	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0020206	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001265	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001385	PMID:30401460	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000252	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001344	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002353	PMID:30401460	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002870	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0011968	PMID:30401460	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001382	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000691	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0011800	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001738	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002827	PMID:30401460	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000767	OMIM:618268	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000007	PMID:30401460	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000403	PMID:30401460	PCS		4/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000527	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0007874	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0004209	PMID:30401460	PCS		4/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0003438	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000248	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000369	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002028	PMID:30401460	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000687	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000341	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000540	PMID:30401460	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0011914	PMID:30401460	PCS		4/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002240	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0010665	PMID:30401460	PCS		2/3			P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0012202	PMID:30401460	PCS		3/3			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0010502	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0100027	PMID:30401460	PCS		1/3			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002719	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001629	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0100704	PMID:30401460	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000414	PMID:30401460	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000656	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002714	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000218	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002557	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000774	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001744	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001347	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001622	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002212	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000154	PMID:30401460	PCS		2/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002059	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001561	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002650	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001762	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001321	PMID:30401460	PCS		1/4			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0005684	OMIM:618268	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002570	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001081	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-02-15]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0011344	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0010536	PMID:30401460	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000508	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001558	PMID:30401460	PCS		2/2			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000821	PMID:30401460	PCS		1/3			P	HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000989	PMID:30401460	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002208	PMID:30401460	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0001357	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0000664	PMID:30401460	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:618268	Trichohepatoneurodevelopmental syndrome		HP:0002721	PMID:30401460	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-26]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0003774	PMID:22510444;PMID:23692385	PCS		3/4			P	HPO:probinson[2021-09-06];HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0007737	PMID:23692385	PCS		1/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0003577	PMID:23692385	PCS		2/2			C	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001696	PMID:22510444	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001156	PMID:22510444	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001651	PMID:22510444	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0010442	PMID:22510444	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0100543	PMID:22510444	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000458	PMID:23692385	PCS		1/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0007401	PMID:23692385	PCS		1/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0006159	PMID:23692385	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000510	PMID:23692385	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000135	PMID:22510444	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001249	PMID:23692385	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0002311	PMID:22510444	PCS		1/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000054	PMID:17163542	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001162	PMID:23692385	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001263	PMID:22510444	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0100260	PMID:22510444	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001959	PMID:22510444;PMID:23692385	PCS		3/4			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000107	PMID:23692385	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000007	PMID:22510444	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000546	PMID:22510444	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0004409	PMID:23692385	PCS		1/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000505	PMID:23692385	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000548	PMID:22510444	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001830	PMID:23692385	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0000103	PMID:23692385	PCS		2/2			P	HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0001513	PMID:22510444	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-09-06]
OMIM:615994	Bardet-Biedl syndrome 17		HP:0004689	PMID:23692385	PCS		1/2			P	HPO:probinson[2021-09-06]
OMIM:220500	Doors syndrome		HP:0000286	PMID:17994565	PCS		8/19			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0003676	OMIM:220500	TAS					C	HPO:skoehler[2012-10-17]
OMIM:220500	Doors syndrome		HP:0000365	OMIM:220500	TAS					P	HPO:probinson[2009-02-17]
OMIM:220500	Doors syndrome		HP:0001250	PMID:17994565	PCS		27/31			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001252	OMIM:220500	IEA					P	HPO:iea[2009-02-17]
OMIM:220500	Doors syndrome		HP:0001290	PMID:17994565	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000280	PMID:17994565	PCS		14/18			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000518	OMIM:220500	IEA					P	HPO:iea[2009-02-17]
OMIM:220500	Doors syndrome		HP:0001804	PMID:17994565	PCS		30/30			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000316	PMID:17994565	PCS		8/15			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001800	PMID:17994565	PCS		31/31			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001643	PMID:17994565	PCS		2/30			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001249	PMID:17994565	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001265	PMID:17994565	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000175	PMID:17994565	PCS		4/24			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000252	PMID:17994565	PCS		7/26			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001263	PMID:17994565	PCS		24/24			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000294	PMID:17994565	PCS		5/15			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0011003	OMIM:220500	IEA					P	HPO:iea[2009-02-17]
OMIM:220500	Doors syndrome		HP:0032524	PMID:17994565	PCS		17/28			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000407	PMID:17994565	PCS		27/27			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000800	OMIM:220500	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:220500	Doors syndrome		HP:0000007	PMID:17994565	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000648	PMID:17994565	PCS		8/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0004209	PMID:17994565	PCS		9/29			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000369	PMID:17994565	PCS		10/17			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000341	PMID:17994565	PCS		12/17			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001199	PMID:17994565	PCS		9/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0003577	PMID:17994565	PCS		1/1			C	HPO:probinson[2022-08-14]
OMIM:220500	Doors syndrome		HP:0000343	PMID:17994565	PCS		19/20			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000463	PMID:17994565	PCS		18/20			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001271	PMID:17994565	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0012402	PMID:17994565	PCS					P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001629	PMID:17994565	PCS	HP:0003577	3/30			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000618	OMIM:220500	IEA					P	HPO:iea[2009-02-17]
OMIM:220500	Doors syndrome		HP:0009882	PMID:17994565	PCS		30/30			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000414	PMID:17994565	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001305	OMIM:220500	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:220500	Doors syndrome		HP:0000219	PMID:17994565	PCS		13/21			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0002119	OMIM:220500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220500	Doors syndrome		HP:0002714	PMID:17994565	PCS		15/18			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000218	PMID:17994565	PCS		7/20			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000212	PMID:17994565	PCS		3/3			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000179	PMID:17994565	PCS		14/19			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0002059	OMIM:220500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220500	Doors syndrome		HP:0008619	OMIM:220500	TAS					P	HPO:probinson[2009-02-17]
OMIM:220500	Doors syndrome		HP:0000431	PMID:17994565	PCS		18/19			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000232	OMIM:220500	IEA					P	HPO:iea[2009-02-17]
OMIM:220500	Doors syndrome		HP:0000474	PMID:17994565	PCS	HP:0030674	3/5			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000194	PMID:17994565	PCS		12/17			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0000508	PMID:17994565	PCS		4/16			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0009237	PMID:17994565	PCS		21/29			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001631	PMID:17994565	PCS	HP:0003577	2/30			P	HPO:probinson[2020-09-19]
OMIM:220500	Doors syndrome		HP:0001798	OMIM:220500	TAS					P	HPO:probinson[2009-02-17]
OMIM:220500	Doors syndrome		HP:0000104	OMIM:220500	TAS		HP:0040283			P	HPO:skoehler[2013-04-18]
OMIM:224000	Dysautonomia-Like disorder		HP:0012332	OMIM:224000	IEA					P	HPO:skoehler[2015-01-27]
OMIM:224000	Dysautonomia-Like disorder		HP:0009830	OMIM:224000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:224000	Dysautonomia-Like disorder		HP:0000007	OMIM:224000	IEA					I	HPO:iea[2009-02-17]
OMIM:224000	Dysautonomia-Like disorder		HP:0001249	OMIM:224000	IEA					P	HPO:iea[2009-02-17]
OMIM:193000	Vesicoureteral reflux 1		HP:0000076	OMIM:193000	IEA					P	HPO:iea[2009-02-17]
OMIM:193000	Vesicoureteral reflux 1		HP:0000924	OMIM:193000	IEA					P	HPO:iea[2009-02-17]
OMIM:193000	Vesicoureteral reflux 1		HP:0001426	OMIM:193000	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:193000	Vesicoureteral reflux 1		HP:0000006	OMIM:193000	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0004325	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0010913	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0002591	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0003593	PMID:36239646	PCS		2/2			C	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0010911	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0010910	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0001508	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0011342	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0001954	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0001987	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0002789	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0000006	PMID:36239646	PCS					I	HPO:probinson[2023-02-28]
OMIM:620085	Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2		HP:0003138	PMID:36239646	PCS		2/2			P	HPO:probinson[2023-02-28]
OMIM:617629	Schizophrenia 19		HP:0100543	PMID:28628109	PCS		4/26			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:617629	Schizophrenia 19		HP:0003596	PMID:28628109	PCS		1/15			C	HPO:probinson[2023-04-08]
OMIM:617629	Schizophrenia 19		HP:0100753	PMID:28628109	PCS		9/26			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:617629	Schizophrenia 19		HP:0011462	PMID:28628109	PCS		14/15			C	HPO:probinson[2023-04-08]
OMIM:617629	Schizophrenia 19		HP:0003829	PMID:28628109	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-08]
OMIM:617629	Schizophrenia 19		HP:0007302	PMID:28628109	PCS		4/26			P	HPO:probinson[2023-04-08]
OMIM:617629	Schizophrenia 19		HP:0000006	PMID:28628109	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0001397	PMID:22768673	PCS		1/1			P	HPO:probinson[2023-03-02]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0003621	PMID:22768673	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2023-03-02]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0000793	OMIM:608709	IEA					P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0000100	OMIM:608709	IEA					P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0005421	OMIM:608709	IEA					P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0000790	OMIM:608709	IEA					P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0000093	OMIM:608709	IEA					P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0000819	OMIM:608709	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0009056	PMID:22768673	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0002719	OMIM:608709	IEA					P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0009002	PMID:22768673	PCS		1/1			P	HPO:probinson[2012-06-22]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0000147	OMIM:608709	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0003745	OMIM:608709	IEA					I	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0003119	OMIM:608709	TAS					P	HPO:skoehler[2012-10-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0009019	PMID:22768673	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0000006	PMID:22768673	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-02]
OMIM:608709	Lipodystrophy, partial, acquired, susceptibility to		HP:0001007	OMIM:608709	TAS					P	HPO:skoehler[2012-10-17]
OMIM:117300	Dementia, familial danish		HP:0000709	OMIM:117300	TAS					P	HPO:iea[2009-02-17]
OMIM:117300	Dementia, familial danish		HP:0000365	OMIM:117300	TAS					P	HPO:iea[2009-02-17]
OMIM:117300	Dementia, familial danish		HP:0011970	PMID:20385796	PCS					P	HPO:iea[2015-02-01]
OMIM:117300	Dementia, familial danish		HP:0000726	OMIM:117300	TAS					P	HPO:iea[2009-02-17]
OMIM:117300	Dementia, familial danish		HP:0001251	PMID:20385796	PCS					P	HPO:iea[2015-02-01]
OMIM:117300	Dementia, familial danish		HP:0002185	PMID:11895040	PCS					P	HPO:iea[2015-02-01]
OMIM:117300	Dementia, familial danish		HP:0001115	OMIM:117300	TAS					P	HPO:iea[2009-02-17]
OMIM:117300	Dementia, familial danish		HP:0002080	OMIM:117300	TAS					P	HPO:iea[2009-02-17]
OMIM:117300	Dementia, familial danish		HP:0001257	PMID:20385796	PCS					P	HPO:iea[2015-02-01]
OMIM:117300	Dementia, familial danish		HP:0000006	OMIM:117300	TAS					I	HPO:probinson[2009-02-17]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0001133	OMIM:612989	TAS					P	HPO:skoehler[2014-10-06]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000486	OMIM:612989	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000980	OMIM:612989	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0001639	OMIM:612989	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000407	OMIM:612989	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0003828	OMIM:612989	TAS					M	HPO:skoehler[2015-12-30]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000007	PMID:19327736	PCS					I	HPO:skoehler[2013-01-09]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0007641	OMIM:612989	TAS					P	HPO:skoehler[2014-10-06]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0007663	OMIM:612989	TAS				HP:0012832	P	HPO:skoehler[2015-07-26]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000505	PMID:19327736	PCS	HP:0011463				P	HPO:skoehler[2013-02-23]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000648	OMIM:612989	TAS					P	HPO:skoehler[2014-10-06]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000603	PMID:19327736	PCS	HP:0011463				P	HPO:skoehler[2013-02-23]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000543	PMID:19327736	PCS					P	HPO:skoehler[2013-02-23]
OMIM:612989	Optic atrophy 7 with or without auditory neuropathy		HP:0000666	OMIM:612989	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0001397	PMID:27862896	PCS		1/3			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003202	PMID:27862896	PCS		3/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003236	PMID:27862896	PCS		1/3			P	HPO:skoehler[2015-02-22];HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0001761	PMID:27862896	PCS		3/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003077	PMID:27862896	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003198	PMID:27862896	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003551	PMID:27862896	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0001010	PMID:27862896	PCS		2/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003560	OMIM:615980	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0012743	OMIM:615980	IEA					P	HPO:skoehler[2015-01-19]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0000819	OMIM:615980	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0007340	PMID:27862896	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0011462	PMID:27862896	PCS		3/3			C	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0002938	PMID:27862896	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0000822	PMID:27862896	PCS		2/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0000855	OMIM:615980	TAS					P	HPO:skoehler[2014-09-21]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0000007	OMIM:615980	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0009125	PMID:27862896	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0000956	PMID:27862896	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0001324	PMID:27862896	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003701	OMIM:615980	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615980	Lipodystrophy, familial partial, type 6		HP:0003119	OMIM:615980	TAS					P	HPO:skoehler[2014-09-21]
OMIM:613329	Plasminogen activator inhibitor-1 deficiency		HP:0001892	OMIM:613329	TAS					P	HPO:probinson[2012-07-16]
OMIM:613329	Plasminogen activator inhibitor-1 deficiency		HP:0000132	OMIM:613329	TAS					P	HPO:probinson[2012-07-16]
OMIM:613329	Plasminogen activator inhibitor-1 deficiency		HP:0003577	OMIM:613329	TAS					C	HPO:probinson[2012-07-16]
OMIM:613329	Plasminogen activator inhibitor-1 deficiency		HP:0000007	OMIM:613329	TAS					I	HPO:probinson[2012-07-16]
OMIM:613329	Plasminogen activator inhibitor-1 deficiency		HP:0000006	OMIM:613329	TAS					I	HPO:probinson[2012-07-16]
OMIM:113600	Branchial cleft anomaliesbranchial cysts, included		HP:0000464	OMIM:113600	IEA					P	HPO:iea[2009-02-17]
OMIM:113600	Branchial cleft anomaliesbranchial cysts, included		HP:0000006	OMIM:113600	IEA					I	HPO:iea[2009-02-17]
OMIM:615758	Immunodeficiency 22		HP:0002960	PMID:22985903	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0025188	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0005479	PMID:9664084	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0002783	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0004385	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0003593	PMID:9664084	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0001508	PMID:9664084;PMID:22985903	PCS		2/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12];HPO:skoehler[2014-08-24];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0001903	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0011463	PMID:22985903	PCS		1/1			C	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0001701	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0001945	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0012490	PMID:22985903	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0025615	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0004315	PMID:9664084	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0002850	PMID:9664084	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0002014	PMID:9664084	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0030005	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0001541	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0009098	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0000007	PMID:9664084	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0002788	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0001873	PMID:22985903	PCS		1/1			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0002720	PMID:9664084	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:615758	Immunodeficiency 22		HP:0002721	PMID:9664084	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-12]
OMIM:147251	Incisors, fused mandibular		HP:0000164	OMIM:147251	IEA					P	HPO:iea[2009-02-17]
OMIM:147251	Incisors, fused mandibular		HP:0000006	OMIM:147251	IEA					I	HPO:iea[2009-02-17]
OMIM:166710	OSTEOPOROSIS		HP:0000939	OMIM:166710	IEA					P	HPO:iea[2009-02-17]
OMIM:166710	OSTEOPOROSIS		HP:0000006	OMIM:166710	IEA					I	HPO:iea[2009-02-17]
OMIM:180295	Rhabdomyosarcoma, embryonal, 2		HP:0030983	PMID:21882293	PCS					P	HPO:nvasilevsky[2018-06-13]
OMIM:180295	Rhabdomyosarcoma, embryonal, 2		HP:0100528	PMID:21882293	PCS					P	HPO:nvasilevsky[2018-06-13]
OMIM:180295	Rhabdomyosarcoma, embryonal, 2		HP:0025388	PMID:21882293	PCS	HP:0003621				P	HPO:nvasilevsky[2018-06-13]
OMIM:180295	Rhabdomyosarcoma, embryonal, 2		HP:0002667	PMID:21882293	PCS	HP:0011463				P	HPO:nvasilevsky[2018-06-13]
OMIM:180295	Rhabdomyosarcoma, embryonal, 2		HP:0006743	PMID:21882293	PCS					P	HPO:skoehler[2015-08-22]
OMIM:180295	Rhabdomyosarcoma, embryonal, 2		HP:0000853	PMID:21882293	PCS	HP:0003621				P	HPO:nvasilevsky[2018-06-13]
OMIM:180295	Rhabdomyosarcoma, embryonal, 2		HP:0005987	PMID:21882293	PCS	HP:0003621				P	HPO:skoehler[2015-08-22]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001276	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0003676	PMID:20647552	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002169	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001410	OMIM:614877	TAS					P	HPO:probinson[2013-02-24]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001310	PMID:20647552	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001272	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002066	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002063	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0003593	PMID:20647552	PCS		2/4			C	HPO:probinson[2022-11-01];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001251	PMID:20647552	PCS		2/4			P	HPO:probinson[2013-02-24];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002061	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0012444	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0000639	PMID:20647552	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001508	OMIM:614877	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0000518	PMID:20647552	PCS		3/4			P	HPO:probinson[2013-02-24];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0011463	PMID:20647552	PCS		2/4			C	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0010571	PMID:20647552	PCS		6/6			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002317	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002359	PMID:20647552	PCS		2/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002415	PMID:20647552	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002019	PMID:20647552	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002313	PMID:20647552	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0000556	OMIM:614877	TAS					P	HPO:probinson[2013-02-24]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001249	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001348	PMID:20647552	PCS		2/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0200085	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0006855	PMID:20647552	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002015	PMID:20647552	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0003487	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001260	PMID:20647552	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001263	OMIM:614877	TAS					P	HPO:probinson[2013-02-24]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0012534	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0011448	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0011096	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0007371	PMID:20647552	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0008167	PMID:20647552	PCS		6/6			P	HPO:probinson[2013-02-24];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0009830	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0000007	PMID:20647552	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0000505	OMIM:614877	TAS					P	HPO:probinson[2013-02-24]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0000648	PMID:20647552	PCS		1/4			P	HPO:probinson[2013-02-24];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001319	OMIM:614877	TAS					P	HPO:probinson[2013-02-24]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0030051	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002505	PMID:20647552	PCS		2/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0001257	PMID:20647552	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0000666	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:614877	Peroxisome biogenesis disorder 8B		HP:0002500	PMID:20647552	PCS		1/4			P	HPO:probinson[2022-11-01]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0001067	PMID:9529361	PCS		1/5			P	HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0003596	PMID:11704931	PCS		1/3			C	HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0000957	PMID:11704931;PMID:9529361	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0001480	PMID:11704931	PCS		0/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0002385	PMID:9529361	PCS		2/5			P	HPO:probinson[2012-04-28];HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0007340	OMIM:162210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0011462	PMID:11704931	PCS		2/3			C	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0006851	OMIM:162210	IEA					P	HPO:iea[2009-02-17]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0009732	PMID:9529361	PCS		1/5			P	HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0009735	PMID:11704931;PMID:9529361	PCS		8/8			P	HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0000006	PMID:9529361	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:162210	Neurofibromatosis, familial spinal		HP:0009737	PMID:11704931;PMID:9529361	PCS		2/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0001287	OMIM:600802	TAS					P	HPO:skoehler[2012-10-16]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0005403	PMID:9354668	PCS		4/4			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0005214	OMIM:600802	TAS					P	HPO:skoehler[2012-10-16]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0002783	PMID:9354668	PCS		4/4			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0004430	PMID:9354668	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0003593	PMID:11668610	PCS		21/24			C	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0005372	PMID:7659163	PCS		2/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0002090	PMID:7481768	PCS	HP:0003593	1/1			P	HPO:skoehler[2012-10-16];HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0033581	PMID:7481768	IEA		1/1			P	HPO:probinson[2021-02-13]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0031382	PMID:9354668	PCS		4/4			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0001508	PMID:9354668	PCS		2/4			P	HPO:skoehler[2012-10-16];HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0001508	PMID:7481768	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0000007	PMID:9354668	PCS					I	HPO:skoehler[2012-10-16];HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0000403	PMID:7481768	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0001888	PMID:7481768	PCS		1/1			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0002788	PMID:9354668	PCS		4/4			P	HPO:skoehler[2012-10-16];HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0002965	OMIM:600802	TAS					P	HPO:skoehler[2012-10-16]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0040219	PMID:9354668	PCS		3/4			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0003347	PMID:9354668	PCS		4/4			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0002028	PMID:9354668	PCS		1/4			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0002028	PMID:7481768	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-31]
OMIM:600802	Scid, autosomal recessive, T-Negative/b-Positive type		HP:0003139	PMID:7659163	TAS		2/2			P	HPO:skoehler[2012-10-16];HPO:probinson[2020-10-31]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001771	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002188	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002540	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0004322	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001371	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0003273	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002460	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0010806	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001290	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000358	PMID:31206972	PCS		20/20			P	HPO:probinson[2023-02-11];HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000175	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000252	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001344	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0011968	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001260	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000490	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001263	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002827	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002307	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0006467	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001257	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000248	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000369	PMID:31206972	PCS					P	HPO:probinson[2023-02-11]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0010628	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000343	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000463	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000540	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000020	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0030319	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0012444	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0009486	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000657	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002119	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001989	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002714	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001423	PMID:31206972	PCS					I	HPO:probinson[2020-07-24]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000774	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0006610	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001347	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001561	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002015	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001762	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002650	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0031936	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000470	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0001838	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0002808	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000308	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000508	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:301041	Wieacker-Wolff syndrome, female-restricted		HP:0000348	PMID:31206972	PCS					P	HPO:probinson[2020-07-25]
OMIM:243500	Isovaleric acidemia		HP:0001254	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0001993	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0002013	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0001882	OMIM:243500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:243500	Isovaleric acidemia		HP:0001250	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0001263	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:6000602	PMID:17850781	PCS		4/4			P	HPO:probinson[2024-04-03]
OMIM:243500	Isovaleric acidemia		HP:0011695	OMIM:243500	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:243500	Isovaleric acidemia		HP:4000210	OMIM:243500	TAS					P	HPO:probinson[2024-01-06]
OMIM:243500	Isovaleric acidemia		HP:0001944	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0000007	OMIM:243500	IEA					I	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0005528	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:6001063	PMID:38484105;PMID:16602101;PMID:33521113	PCS		30/30			P	HPO:probinson[2024-08-03]
OMIM:243500	Isovaleric acidemia		HP:0003108	OMIM:243500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:243500	Isovaleric acidemia		HP:0001873	OMIM:243500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:243500	Isovaleric acidemia		HP:0001876	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0001942	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:243500	Isovaleric acidemia		HP:0001259	OMIM:243500	IEA					P	HPO:iea[2009-02-17]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0002540	PMID:29784083	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0001344	PMID:29784083	PCS		2/2			P	HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0011182	PMID:29784083	PCS		1/1			P	HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0001263	PMID:29784083	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0001252	PMID:29784083	PCS		2/2			P	HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0003593	PMID:29784083	PCS		2/2			C	HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0032794	PMID:29784083	PCS		2/2			P	HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0000007	PMID:29784083	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-16]
OMIM:618095	Intellectual developmental disorder, autosomal recessive 63		HP:0001257	PMID:29784083	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001254	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0003210	PMID:20556797	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001252	PMID:35712814	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0002240	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0003593	PMID:12471062	PCS		1/5			C	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0033443	PMID:35712814	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0002919	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001508	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001903	OMIM:251110	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0011463	PMID:12471062	PCS		1/5			C	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001944	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0008872	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001987	PMID:35712814	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001943	PMID:35712814	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001946	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0002912	PMID:35712814	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001942	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001644	PMID:35712814	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0003623	PMID:35712814;PMID:12471062;OMIM:251110	PCS		14/16			C	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0003145	PMID:12471062	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0002013	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0002098	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0002154	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001263	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0002194	PMID:35712814	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0032988	PMID:35712814	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0040126	PMID:35712814	PCS		0/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0035024	PMID:35712814	PCS		1/1			P	HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0012120	PMID:35712814;OMIM:251110	PCS		11/11			P	HPO:probinson[2024-03-16];HPO:skoehler[2012-10-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0000007	PMID:12471062	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001873	OMIM:251110	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001876	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001259	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:251110	Methylmalonic aciduria, vitamin B12-responsive, cblB type		HP:0001875	OMIM:251110	IEA					P	HPO:iea[2009-02-17]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001410	OMIM:614863	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001250	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0003196	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001251	PMID:21937992	PCS					P	HPO:probinson[2013-02-24]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0002240	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001290	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000639	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000316	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000954	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000510	OMIM:614863	TAS					P	HPO:probinson[2013-02-24]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000256	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000556	OMIM:614863	TAS					P	HPO:probinson[2013-02-24]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001249	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001288	OMIM:614863	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001263	OMIM:614863	TAS					P	HPO:probinson[2013-02-24]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000070	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000407	OMIM:614863	TAS					P	HPO:probinson[2013-02-24]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000007	OMIM:614863	TAS					I	HPO:probinson[2013-01-09]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001954	OMIM:614863	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0001319	OMIM:614863	TAS					P	HPO:probinson[2013-02-24]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000505	OMIM:614863	TAS					P	HPO:probinson[2013-02-24]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000648	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000846	OMIM:614863	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000762	OMIM:614863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614863	Peroxisome biogenesis disorder 4B		HP:0000006	OMIM:614863	IEA					I	HPO:skoehler[2018-10-08]
OMIM:174300	Orofaciodigital syndrome V		HP:0003577	PMID:28711741;PMID:23972372;PMID:29127725	PCS		11/11			C	HPO:probinson[2022-03-21];ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0000365	PMID:28711741	PCS		2/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001212	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0000161	PMID:23972372	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001274	PMID:23972372	PCS		1/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000085	PMID:23972372	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0012725	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0000180	PMID:23972372	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0012741	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001629	PMID:23972372	PCS	HP:0003577	1/6			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001629	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0010297	PMID:28711741	PCS		2/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0010296	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000316	PMID:23972372	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0020045	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000219	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000218	PMID:28711741;PMID:29127725	PCS		3/5			P	HPO:probinson[2022-03-21];ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0007687	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0004736	PMID:23972372	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0001249	PMID:23972372;PMID:29127725	PCS		8/8			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21];ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0000175	PMID:28711741;PMID:23972372	PCS		3/9			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000494	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000252	PMID:28711741;PMID:29127725	PCS		4/5			P	HPO:probinson[2022-03-21];ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0002650	PMID:23972372	PCS		1/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000574	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0011968	PMID:28711741	PCS		3/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0002197	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0001162	PMID:23972372	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000193	PMID:23972372	PCS		4/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001263	PMID:28711741;PMID:29127725	PCS		5/5			P	HPO:probinson[2022-03-21];ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0002251	PMID:23972372	PCS		1/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0025190	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0011802	PMID:28711741	IEA		3/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0100025	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0100259	PMID:28711741;PMID:23972372;PMID:29127725	PCS		9/11			P	HPO:probinson[2022-03-21];ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0000668	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001636	PMID:23972372	PCS	HP:0003577	1/6			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000007	PMID:23972372	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000689	PMID:29127725	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0004209	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0007236	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0002007	PMID:23972372	PCS		6/6			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001830	PMID:23972372	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0002205	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0001852	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000369	PMID:28711741	PCS		3/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000303	PMID:29127725	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-22]
OMIM:174300	Orofaciodigital syndrome V		HP:0000324	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:174300	Orofaciodigital syndrome V		HP:0000588	PMID:28711741	PCS		1/3			P	HPO:probinson[2022-03-21]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0004950	OMIM:126320	PCS					P	HPO:probinson[2012-04-11]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0001629	OMIM:126320	PCS					P	HPO:probinson[2012-04-11]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0002619	OMIM:126320	PCS					P	HPO:probinson[2012-04-11]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0010741	OMIM:126320	PCS					P	HPO:probinson[2012-04-11]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0009743	OMIM:126320	PCS					P	HPO:probinson[2012-04-11]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0001643	OMIM:126320	PCS					P	HPO:probinson[2012-04-11]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0000006	OMIM:126320	PCS					I	HPO:probinson[2012-04-11]
OMIM:126320	Distichiasis with congenital anomalies of the heart and peripheral		HP:0001688	OMIM:126320	PCS					P	HPO:probinson[2012-04-11]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0003577	PMID:15468086;PMID:15236405;PMID:10508519	PCS		5/7			C	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001252	PMID:10508519	PCS	HP:0003577	3/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001252	PMID:15468086	PCS		2/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001252	PMID:15236405	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001270	PMID:15468086	PCS		2/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0030319	PMID:15468086;PMID:10508519	PCS		6/6			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0100297	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0100309	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0002878	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0003803	PMID:10508519	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0000218	PMID:15468086	PCS		2/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001522	PMID:19553116;PMID:10508519	PCS		3/4			C	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001623	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0003623	PMID:15468086	PCS		1/3			C	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0003202	PMID:10508519	PCS		3/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0000275	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0032989	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001342	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0002015	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0003324	PMID:15468086	PCS		3/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0000276	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0000298	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0011968	PMID:10508519	PCS		3/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0002098	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001284	PMID:10508519	PCS		3/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0033454	PMID:15236405	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0010310	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0011471	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0034392	PMID:15236405	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0003819	PMID:15468086	PCS		1/3			C	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0012084	PMID:15236405	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0034671	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0009473	PMID:19553116	PCS		1/1			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0034198	PMID:19553116	PCS		1/1			C	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0040288	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0001558	PMID:15468086;PMID:19553116;PMID:10508519	PCS		5/7			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0002943	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0000006	PMID:10508519	PCS					I	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0000303	PMID:15468086	PCS		1/3			P	HPO:probinson[2023-07-07]
OMIM:620278	Congenital myopathy 2C, severe infantile, autosomal dominant		HP:0003798	PMID:15236405;PMID:19553116	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000365	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0002186	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001250	PMID:36401616	PCS		7/7			P	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000160	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001252	PMID:36401616	PCS		4/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0003196	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0002020	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0003593	PMID:36401616	PCS		2/7			C	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0011463	PMID:36401616	PCS		3/7			C	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000718	PMID:36401616	PCS		4/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0011220	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0012471	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000717	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000316	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000278	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001249	PMID:36401616	PCS		7/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000494	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001263	PMID:36401616	PCS		4/4			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001182	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0034353	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000007	PMID:36401616	PCS					I	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001338	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000527	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000400	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0002942	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000685	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000520	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000322	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0003577	PMID:36401616	PCS		2/7			C	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000582	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000343	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000189	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001274	PMID:36401616	PCS		3/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001270	PMID:36401616	PCS		6/6			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000739	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0008551	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000657	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001548	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000337	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000256	PMID:36401616	PCS		5/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001347	PMID:36401616	PCS		3/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000275	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000154	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0002213	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0002650	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000431	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000592	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000470	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000668	PMID:36401616	PCS		3/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0002007	PMID:36401616	PCS		2/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000664	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0000347	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:620250	Neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum		HP:0001513	PMID:36401616	PCS		1/7			P	HPO:probinson[2023-07-09]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0002069	PMID:31300657	PCS		7/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0002540	PMID:31300657	PCS		4/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0001332	PMID:31300657	PCS		1/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0001272	PMID:31300657	PCS		6/23			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0002066	PMID:31300657	PCS		1/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0020221	PMID:31300657	PCS		3/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0000733	PMID:31300657	PCS		2/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0012171	PMID:31300657	PCS					P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0001249	PMID:31300657	PCS		28/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0000253	PMID:31300657	PCS	HP:0003593	4/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0002059	PMID:31300657	PCS		4/23			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0001344	PMID:31300657	PCS		14/25			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0000750	PMID:31300657	PCS		11/25			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0001762	PMID:31300657	PCS	HP:0003577	1/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0002373	PMID:31300657	PCS		1/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0001263	PMID:31300657	PCS		28/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0002072	PMID:31300657	PCS		1/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0032792	PMID:31300657	PCS		1/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0000729	PMID:31300657	PCS		17/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0000722	PMID:31300657	PCS		2/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0100716	PMID:31300657	PCS		1/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0007359	PMID:31300657	PCS		8/28			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0001257	PMID:31300657	PCS		1/22			P	HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0000006	PMID:31300657	PCS					I	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618917	Neurodevelopmental disorder with language impairment and behavioral abnormalities		HP:0000028	PMID:31300657	PCS		1/15	MALE		P	HPO:probinson[2020-08-11]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0000121	PMID:23553769	PCS		3/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0002188	PMID:23553769	PCS		1/12			P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0004840	PMID:23553769	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0003355	PMID:23553769	PCS		7/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001250	PMID:23553769	PCS		5/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001252	PMID:23553769	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001251	PMID:23553769	PCS		4/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0003593	PMID:23553769	PCS		6/12			C	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001290	PMID:23553769	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0011463	PMID:23553769	PCS		1/12			C	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001924	PMID:23553769	PCS	HP:0003593	12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0000510	PMID:23553769	PCS		3/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001744	PMID:23553769	PCS		4/11			P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0003128	PMID:23553769	PCS		3/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0003623	PMID:23553769	PCS		5/12			C	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0008936	PMID:23553769	PCS					P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0002059	PMID:23553769	PCS		4/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0004313	PMID:23553769	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0002299	PMID:23553769	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001981	PMID:23553769	PCS					P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001263	PMID:23553769	PCS		11/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0002194	PMID:23553769	PCS					P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0032323	PMID:23553769	PCS					P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0010976	PMID:23553769	PCS		11/12			P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0000407	PMID:23553769	PCS		5/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0000007	PMID:23553769	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001638	PMID:23553769	PCS		2/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001334	PMID:23553769	PCS		1/12			P	HPO:probinson[2020-11-03]
OMIM:616084	Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay		HP:0001510	PMID:23553769	PCS		HP:0040283			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-11-03]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0003774	PMID:7987396	PCS		3/6			P	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0003621	PMID:7987396	PCS		4/6			C	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0008619	PMID:7987396	PCS		1/6			P	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0000365	PMID:7987396	PCS		1/6			P	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0000100	PMID:7987396	PCS		1/6			P	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0000083	PMID:7987396	PCS		6/6			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0000093	PMID:7987396	PCS		3/3			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0012577	PMID:7987396	PCS		1/6			P	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0011463	PMID:7987396	PCS		2/6			C	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0002907	PMID:7987396	PCS		6/6			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0000407	PMID:7987396	PCS		1/6			P	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0012592	PMID:7987396	PCS		1/6			P	HPO:probinson[2024-03-12]
OMIM:620536	Alport syndrome 3B, autosomal recessive		HP:0000007	PMID:7987396	PCS					I	HPO:probinson[2024-03-12]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0000286	OMIM:133705	TAS					P	HPO:skoehler[2015-12-30]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0001374	OMIM:133705	TAS					P	HPO:skoehler[2015-12-30]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0001838	OMIM:133705	IEA					P	HPO:iea[2009-02-17]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0002021	OMIM:133705	IEA					P	HPO:iea[2009-02-17]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0000954	OMIM:133705	IEA					P	HPO:iea[2009-02-17]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0007598	OMIM:133705	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0009237	OMIM:133705	IEA					P	HPO:iea[2009-02-17]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0000405	OMIM:133705	TAS					P	HPO:skoehler[2015-12-30]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0000006	OMIM:133705	IEA					I	HPO:iea[2009-02-17]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0000413	OMIM:133705	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:133705	External auditory canal, bilateral atresia of, with congenital verticaltalus		HP:0000577	OMIM:133705	IEA					P	HPO:iea[2009-02-17]
OMIM:175750	Popliteal cyst		HP:0001386	PMID:5080689	PCS					P	HPO:lccarmody[2018-10-04]
OMIM:175750	Popliteal cyst		HP:0002815	OMIM:175750	IEA					P	HPO:skoehler[2009-02-17]
OMIM:175750	Popliteal cyst		HP:0000006	OMIM:175750	IEA					I	HPO:iea[2009-02-17]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001298	PMID:28583327	PCS		5/34			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001695	PMID:28583327	PCS		1/34			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0003234	OMIM:246450	TAS					P	HPO:skoehler[2013-11-18]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001992	OMIM:246450	IEA					P	HPO:iea[2009-02-17]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0000980	PMID:28583327	PCS		10/34			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001250	PMID:28583327	PCS		17/34			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001252	PMID:28583327	PCS		11/34			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002240	PMID:28583327	PCS		13/34			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0003150	OMIM:246450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0410051	PMID:23705938	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:6000216	PMID:28583327	PCS		13/13			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0031962	PMID:28583327	PCS		9/10			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0031964	PMID:28583327	PCS		14/20			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002919	PMID:28583327	PCS		2/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001903	OMIM:246450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0033596	PMID:28583327	PCS					P	HPO:probinson[2024-02-27];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001944	PMID:28583327	PCS		3/34			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001987	PMID:28583327	PCS		19/20			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001943	PMID:28583327	PCS		25/28			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001945	PMID:28583327	PCS		3/34			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001942	PMID:28583327	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002014	PMID:28583327	PCS		3/34			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001265	PMID:28583327	PCS		2/34			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0031956	PMID:28583327	PCS		14/20			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0000252	PMID:28583327	PCS		1/34			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002353	OMIM:246450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0003344	PMID:28583327	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0410066	PMID:22626821	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002572	PMID:28583327	PCS		17/34			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001263	PMID:28583327	PCS		17/35			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002151	PMID:28583327	PCS		7/12			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001262	OMIM:246450	IEA					P	HPO:iea[2009-02-17]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0003819	OMIM:246450	IEA					C	HPO:iea[2009-02-17]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0032198	PMID:28583327	PCS		6/20			P	HPO:skoehler[2019-02-22];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0000007	PMID:28583327	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002329	PMID:28583327	PCS		13/34			P	HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0000741	PMID:28583327	PCS		13/34			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001257	PMID:28583327	PCS		1/34			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-02-27]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002500	OMIM:246450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001259	OMIM:246450	IEA					P	HPO:iea[2009-02-17]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0002149	OMIM:246450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:246450	3-hydroxy-3-methylglutaryl-CoA lyase deficiency		HP:0001336	PMID:28583327	PCS		5/34			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-02-27]
OMIM:614687	Alar cleft, isolated		HP:0003745	PMID:19921637	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-04-20]
OMIM:614687	Alar cleft, isolated		HP:0003191	PMID:19921637	PCS					P	HPO:probinson[2019-04-20]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0001760	PMID:21937992	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0001650	PMID:21937992	PCS	HP:0011461	1/4			P	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0000252	PMID:21937992	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0002059	PMID:22633631	PCS		1/4		HP:0012825	P	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0002188	PMID:22633631	PCS		3/4			P	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0000750	PMID:22633631	PCS		4/4			P	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0003487	PMID:22633631	PCS		1/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0002079	PMID:22633631	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0001263	PMID:22633631	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0005484	PMID:22633631	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0003593	PMID:21937992	PCS		2/4			C	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0000639	PMID:22633631	PCS		1/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0011461	PMID:21937992	PCS		2/4			C	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0001647	PMID:22633631	PCS		1/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0000007	PMID:21937992	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0000238	PMID:22633631	PCS	HP:0011461	1/4			P	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0007256	PMID:22633631	PCS		1/4			P	HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0001257	PMID:22633631	PCS		3/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0001249	PMID:21937992;PMID:22633631	PCS		6/6			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:615599	Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity		HP:0001347	PMID:22633631	PCS		2/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2022-03-15]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000286	PMID:33159883	PCS		3/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000582	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001377	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0010747	PMID:33159883	PCS		5/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001250	PMID:33159883	PCS		2/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001252	PMID:33159883	PCS		5/13			P	HPO:probinson[2022-05-07];HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0003593	PMID:33159883	PCS		6/13			C	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0012745	PMID:33159883	PCS		6/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0031987	PMID:33159883	PCS		2/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0006094	PMID:33159883	PCS		3/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0011463	PMID:33159883	PCS		7/13			C	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000718	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000739	PMID:33159883	PCS		2/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0012450	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000712	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000219	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000752	PMID:33159883	PCS		3/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001763	PMID:33159883	PCS		3/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001840	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001249	PMID:33159883	PCS		11/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000358	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0002553	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001385	PMID:33159883	PCS	HP:0003577	1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000750	PMID:33159883	PCS		2/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001762	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0002373	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0002099	PMID:33159883	PCS		4/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000490	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0011800	PMID:33159883	PCS		5/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0012520	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0033000	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000508	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0030890	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000403	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000348	PMID:33159883	PCS		3/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0004209	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0007874	PMID:33159883	PCS		2/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001511	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0001973	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0007018	PMID:33159883	PCS		3/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000303	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0000006	PMID:33159883	PCS					I	HPO:probinson[2022-05-07]
OMIM:301069	Chromosome Xq13 duplication syndrome		HP:0005338	PMID:33159883	PCS		1/13			P	HPO:probinson[2022-05-07]
OMIM:620244	Lymphatic malformation 13		HP:0000343	PMID:30055085	PCS		2/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0006528	PMID:33569873	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0030674	PMID:26036949	PCS		10/10			C	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001195	PMID:33569873	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001790	PMID:26036949	PCS	HP:0030674	10/10			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001790	PMID:30055085	PCS		5/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0000280	PMID:33569873	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0000319	PMID:30055085	PCS		2/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0011220	PMID:30055085	PCS		2/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0000316	PMID:30055085;PMID:33569873	PCS		3/6			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0500049	PMID:33569873	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001643	PMID:30055085;PMID:33569873	PCS		2/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0009900	PMID:33569873	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001004	PMID:30055085	PCS		0/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001048	PMID:33569873	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001028	PMID:30055085	PCS		4/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0025671	PMID:30055085	PCS		0/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001541	PMID:30055085	PCS		5/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0000034	PMID:30055085	PCS		3/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0025676	PMID:30055085	PCS		4/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0002092	PMID:33569873	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0005280	PMID:30055085	PCS		2/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0034198	PMID:30055085;PMID:33569873	PCS		4/4			C	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0000007	PMID:26036949	PCS					I	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0003811	PMID:30055085	PCS		1/5			C	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001631	PMID:30055085;PMID:33569873	PCS		3/5			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001653	PMID:30055085	PCS		2/4			P	HPO:probinson[2023-06-16]
OMIM:620244	Lymphatic malformation 13		HP:0001655	PMID:30055085	PCS		2/4			P	HPO:probinson[2023-06-16]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0003577	PMID:31630791	PCS		3/3			C	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000563	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0001596	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0004322	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0001394	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0003073	PMID:31630791	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0012202	PMID:31630791	PCS		1/1			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0008070	PMID:31630791	PCS		3/3			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0001808	OMIM:242150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0001508	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000613	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0002910	PMID:31630791	PCS		1/3			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000633	OMIM:242150	TAS					P	HPO:probinson[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0001249	PMID:31630791	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0010837	PMID:31630791	PCS		3/3			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0002059	PMID:31630791	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0001263	PMID:31630791	PCS		3/3			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0030948	PMID:31630791	PCS		0/3			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0011967	PMID:31630791	PCS		3/3			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0008064	OMIM:242150	IEA		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000407	PMID:31630791	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000509	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0009830	PMID:31630791	PCS		0/3			P	HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000007	PMID:31630791	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0001019	PMID:31630791	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000982	PMID:31630791	PCS		1/3			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:242150	Ichthyosiform erythroderma, corneal involvement, and deafness		HP:0000545	OMIM:242150	IEA					P	HPO:iea[2009-02-17]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0002223	PMID:12740761	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0000561	PMID:12740761	PCS		4/4			P	HPO:probinson[2012-03-02];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0000164	PMID:12740761	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0001597	PMID:12740761	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0000034	PMID:12740761	PCS		2/2	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0001596	PMID:12740761	PCS		1/4			P	HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0003550	PMID:12740761	PCS		3/4			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0001790	PMID:12740761	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0003593	PMID:12740761	PCS		1/5			C	HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0100540	PMID:12740761	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0034197	PMID:12740761	PCS		1/5			C	HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0100869	PMID:12740761	PCS		2/4			P	HPO:probinson[2012-06-10];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0011463	PMID:12740761	PCS		3/5			C	HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0002209	PMID:12740761	PCS		4/4			P	HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0000007	PMID:12740761	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0000971	PMID:12740761	PCS		0/5			P	HPO:skoehler[2013-06-10];HPO:probinson[2023-02-08]
OMIM:607823	Hypotrichosis-lymphedema-telangiectasia syndrome		HP:0000963	PMID:12740761	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-08]
OMIM:613856	Achromatopsia 4		HP:0000639	PMID:12077706	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:613856	Achromatopsia 4		HP:0000613	PMID:12077706	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:613856	Achromatopsia 4		HP:0000007	PMID:12077706	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:613856	Achromatopsia 4		HP:0000505	PMID:12077706	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:613856	Achromatopsia 4		HP:0011516	PMID:12077706	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:277100	VALINEMIA		HP:0002487	OMIM:277100	IEA					P	HPO:iea[2009-02-17]
OMIM:277100	VALINEMIA		HP:0002013	OMIM:277100	IEA					P	HPO:iea[2009-02-17]
OMIM:277100	VALINEMIA		HP:0001508	OMIM:277100	IEA					P	HPO:iea[2009-02-17]
OMIM:277100	VALINEMIA		HP:0033088	OMIM:277100	TAS					P	HPO:probinson[2020-08-13]
OMIM:277100	VALINEMIA		HP:0000007	OMIM:277100	IEA					I	HPO:iea[2009-02-17]
OMIM:277100	VALINEMIA		HP:0002329	OMIM:277100	IEA					P	HPO:iea[2009-02-17]
OMIM:277100	VALINEMIA		HP:0001324	OMIM:277100	IEA					P	HPO:iea[2009-02-17]
OMIM:277100	VALINEMIA		HP:0010910	OMIM:277100	TAS					P	HPO:probinson[2012-07-22]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0004432	OMIM:615214	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0002719	PMID:22351933	PCS		1/1			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-24]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0003593	PMID:22351933	PCS		1/1			C	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-24]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0000007	PMID:22351933	PCS					I	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-24]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0012219	PMID:22351933	PCS	HP:0003621	1/1			P	HPO:probinson[2023-03-24]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0002843	PMID:22351933	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-15]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0002205	OMIM:615214	TAS					P	HPO:skoehler[2013-05-07]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0001875	PMID:22351933	PCS		1/1			P	HPO:skoehler[2013-05-07];HPO:probinson[2023-03-24]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0040218	PMID:22351933	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:615214	Agammaglobulinemia 7, autosomal recessive		HP:0003139	PMID:22351933	PCS		1/1			P	HPO:probinson[2023-03-24]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000365	PMID:16501574	PCS		4/4			P	HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000680	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0001092	PMID:16501574	PCS		3/4			P	HPO:probinson[2012-04-01];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0010055	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0009462	OMIM:149730	TAS					P	HPO:probinson[2012-05-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0009740	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0011065	PMID:16501574	PCS		1/4			P	HPO:probinson[2012-04-01];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000316	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0009741	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0009944	OMIM:149730;PMID:16501574	PCS		11/14			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000495	OMIM:149730	TAS					P	HPO:skoehler[2013-05-31]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000494	PMID:16501574	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000691	PMID:16501574	PCS		3/4			P	HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0100583	OMIM:149730	PCS					P	HPO:probinson[2012-04-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0100258	OMIM:149730	TAS					P	HPO:skoehler[2012-10-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0004209	OMIM:149730	TAS					P	HPO:probinson[2012-05-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0009778	PMID:16501574	PCS		3/4			P	HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000006	PMID:16501574	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0002984	OMIM:149730	PCS					P	HPO:probinson[2012-04-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000522	PMID:16501574	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0001199	PMID:16501574	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0001233	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0006297	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0008551	PMID:16501574	PCS		3/4			P	HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000217	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0005707	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000337	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000579	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000378	PMID:16501574	PCS		4/4			P	HPO:probinson[2012-04-01];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000410	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000974	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0007900	OMIM:149730	PCS					P	HPO:probinson[2012-04-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000198	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000670	PMID:16501574	PCS		2/4		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0001245	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0003022	OMIM:149730	PCS					P	HPO:probinson[2012-04-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0032107	OMIM:149730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000506	PMID:16501574	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000509	PMID:16501574	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0007892	OMIM:149730	IEA					P	HPO:iea[2012-04-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000629	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000668	PMID:16501574	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000348	PMID:16501574	PCS		1/4			P	HPO:probinson[2023-02-05]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0008743	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000620	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0007732	OMIM:149730	PCS					P	HPO:probinson[2012-04-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0007656	OMIM:149730	PCS					P	HPO:probinson[2012-04-01]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0003974	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0009637	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:149730	Lacrimoauriculodentodigital syndrome-1		HP:0000104	OMIM:149730	IEA					P	HPO:iea[2009-02-17]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000286	PMID:26637975	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0006768	OMIM:156610	IEA					P	HPO:iea[2009-02-17]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000582	OMIM:156610	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000343	PMID:26637975	PCS		1/3			P	HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000160	PMID:26637975	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000581	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0001252	PMID:26637975	PCS		1/3			P	HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000482	OMIM:156610	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0012745	PMID:26637975	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0001270	OMIM:156610	TAS					P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0012368	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000316	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0001305	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0100807	OMIM:156610	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000218	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0002557	OMIM:156610	TAS					P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0006610	PMID:26637975	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0001249	PMID:26637975	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000358	PMID:26637975	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0006855	OMIM:156610	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000396	PMID:26637975	PCS		1/3			P	HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000175	PMID:26637975	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000252	PMID:26637975	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000750	OMIM:156610	TAS				HP:0012825	P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0002079	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000470	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0034400	PMID:26637975	PCS		3/3			P	HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0005280	PMID:26637975	PCS		2/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000629	OMIM:156610	TAS					P	HPO:skoehler[2015-12-30]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000767	OMIM:156610	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000568	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000006	PMID:26637975	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000248	PMID:26637975	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000369	PMID:26637975	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:156610	Skin creases, congenital symmetric circumferential, 1		HP:0000347	OMIM:156610	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0001276	PMID:31586943	PCS		8/8			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0002510	PMID:31586943	PCS		8/8			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0000252	PMID:31586943;PMID:31735293	PCS		19/21			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0002059	PMID:31735293	PCS		4/13			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0002079	PMID:31586943	PCS		6/6			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0002365	PMID:31586943	PCS		3/6			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0001272	PMID:31586943	PCS		3/6			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0001250	PMID:31735293	PCS		12/14			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0001263	PMID:31586943;PMID:31735293	PCS		22/22			P	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0003593	PMID:31586943	PCS					C	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0025190	PMID:31586943	PCS	HP:0003593	8/8			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0012430	PMID:31586943	PCS					P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0001339	PMID:31586943	PCS		6/6			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0000007	PMID:31586943	PCS					I	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0002119	PMID:31586943	PCS		6/6			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0001302	PMID:31735293	PCS		2/13			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0002126	PMID:31735293	PCS		5/13			P	HPO:probinson[2020-04-29]
OMIM:618730	Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity		HP:0001347	PMID:31586943	PCS		8/8			P	HPO:probinson[2020-04-29]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0003577	PMID:28065471	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0002521	PMID:28065471	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000023	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001250	PMID:28065471	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000581	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001252	PMID:28065471	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001270	PMID:28065471	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0033725	PMID:28065471	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000518	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001508	PMID:28065471	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001629	PMID:28065471	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000316	PMID:28065471	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000954	PMID:28065471	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000414	PMID:28065471	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0002119	PMID:28065471	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000411	OMIM:617403	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000278	OMIM:617403	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0020206	PMID:28065471	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000973	PMID:28065471	PCS		3/3			P	HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0002751	PMID:28065471	PCS		0/3			P	HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000494	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001385	PMID:28065471	PCS		1/3			P	HPO:probinson[2022-11-26];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000054	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000750	PMID:28065471	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001762	PMID:28065471	PCS		1/3			P	HPO:skoehler[2019-04-18]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000431	PMID:28065471	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000298	PMID:28065471	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0004970	PMID:28065471	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001582	PMID:28065471	PCS		3/3			P	HPO:probinson[2022-11-26];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0002171	PMID:28065471	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0012385	PMID:28065471	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0034392	PMID:28065471	PCS		1/3			P	HPO:probinson[2022-11-26];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001519	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001639	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0002827	PMID:28065471	PCS		2/3			P	HPO:skoehler[2019-04-18]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000007	PMID:28065471	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001635	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0003758	PMID:28065471	PCS		3/3			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0006687	PMID:28065471	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000400	PMID:28065471	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0009933	PMID:28065471	PCS		2/3			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0001631	PMID:28065471	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0008689	PMID:28065471	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000028	PMID:28065471	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-22]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000369	PMID:28065471	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000325	PMID:28065471	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26]
OMIM:617403	Cutis laxa, autosomal recessive, type IID		HP:0000621	PMID:28065471	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-26];HPO:probinson[2024-04-22]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000286	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001276	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0002267	PMID:26483087	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0010804	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000343	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001310	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001272	PMID:26483087	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001250	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0002384	PMID:26483087	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0002066	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000283	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0003593	PMID:26483087	PCS		1/1			C	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0007286	PMID:26483087	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000713	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000218	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001249	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001347	PMID:26483087	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0008936	PMID:26483087	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001344	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000750	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000233	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0031936	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0002079	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0030147	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0011968	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001263	PMID:26483087	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0005484	PMID:26483087	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0002509	PMID:26483087	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001317	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000007	PMID:26483087	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-07]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0000505	OMIM:618056	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0004209	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0002104	OMIM:618056	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618056	Neurodevelopmental disorder with cerebellar atrophy and with or without seizures		HP:0001337	OMIM:618056	IEA					P	HPO:skoehler[2018-10-08]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000164	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0001792	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000464	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0002353	OMIM:273400	IEA					P	HPO:skoehler[2010-06-21]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0003057	OMIM:273400	IEA					P	HPO:skoehler[2010-06-21]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0003355	OMIM:273400	IEA					P	HPO:skoehler[2010-06-21]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0011675	OMIM:273400	IEA					P	HPO:skoehler[2010-06-21]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0008070	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0100853	OMIM:273400	TAS					P	HPO:probinson[2012-06-22]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000968	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000007	OMIM:273400	IEA					I	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000579	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0002557	OMIM:273400	TAS					P	HPO:probinson[2012-06-22]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000135	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000377	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0000204	OMIM:273400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:273400	Tetramelic deficiencies, ectodermal dysplasia, deformed ears, andother abnormalities		HP:0001249	OMIM:273400	IEA					P	HPO:iea[2009-02-17]
OMIM:301082	Immunodeficiency 102		HP:0410378	PMID:33876203;PMID:35464398	PCS		5/5			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0002783	PMID:33876203	PCS		4/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0410377	PMID:33876203;PMID:35464398	PCS		3/5			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0002240	PMID:33876203	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0011954	PMID:33876203	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0001904	PMID:33876203	PCS		3/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0011463	PMID:33876203	PCS		3/3			C	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0001903	PMID:33876203	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0100806	PMID:33876203	PCS		3/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0500265	PMID:33876203	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0410305	PMID:35464398	PCS		0/1			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0200043	PMID:33876203	PCS		3/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0004315	PMID:33876203;PMID:35464398	PCS		2/5			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0040218	PMID:33876203	PCS		4/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0002850	PMID:33876203;PMID:35464398	PCS		4/5			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0410301	PMID:35464398	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0002257	PMID:35464398	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0001882	PMID:33876203	PCS		4/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0002110	PMID:33876203;PMID:35464398	PCS		1/5			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0030783	PMID:33876203	PCS		3/3			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0003581	PMID:35464398	PCS		1/1			C	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0001581	PMID:33876203	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0034249	PMID:35464398	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0011109	PMID:35464398	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0011108	PMID:33876203	PCS		3/4			P	HPO:probinson[2022-07-19];HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0010976	PMID:33876203;PMID:35464398	PCS		5/5			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0032170	PMID:35464398	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0001419	PMID:33876203	PCS					I	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0032154	PMID:33876203	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0000821	PMID:33876203	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0001973	PMID:33876203	PCS		3/4			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0002788	PMID:35464398	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:301082	Immunodeficiency 102		HP:0002720	PMID:33876203	PCS		3/4			P	HPO:probinson[2022-07-19]
OMIM:189500	Witkop syndrome		HP:0002213	PMID:11369996	PCS		0/9			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:189500	Witkop syndrome		HP:0001807	OMIM:189500	IEA					P	HPO:probinson[2009-02-17]
OMIM:189500	Witkop syndrome		HP:0011937	PMID:11369996	PCS		9/9			P	HPO:probinson[2024-03-08]
OMIM:189500	Witkop syndrome		HP:0001803	OMIM:189500	IEA					P	HPO:probinson[2009-02-17]
OMIM:189500	Witkop syndrome		HP:0000971	PMID:11369996	PCS		0/9			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:189500	Witkop syndrome		HP:0001598	PMID:11369996	PCS		9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:189500	Witkop syndrome		HP:0006347	PMID:11369996	PCS					P	HPO:probinson[2013-02-25];HPO:probinson[2024-03-08]
OMIM:189500	Witkop syndrome		HP:0000006	PMID:11369996	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:189500	Witkop syndrome		HP:0008070	PMID:11369996	PCS		0/9			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:189500	Witkop syndrome		HP:0006349	PMID:11369996	PCS		9/9			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0002421	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0003577	PMID:22544365	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-18]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0000486	OMIM:614678	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001272	PMID:22544365	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-18]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001371	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001250	OMIM:614678	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001290	PMID:22544365	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-18]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0012473	OMIM:614678	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0000639	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0000657	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001308	OMIM:614678	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001324	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0000556	OMIM:614678	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001347	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001760	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0008936	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0000253	PMID:22544365	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-12-18]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0003202	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0002059	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001344	OMIM:614678	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0011968	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001263	OMIM:614678	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0002350	OMIM:614678	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0002093	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0002827	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0000007	PMID:22544365	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-18]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001510	OMIM:614678	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614678	Pontocerebellar hypoplasia, type 1B		HP:0001257	OMIM:614678	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0004313	PMID:29455859	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0006517	PMID:29455859	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0003819	PMID:29455859	PCS		2/5			C	HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0003593	PMID:29455859	PCS		5/5			C	HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0002093	PMID:29455859	PCS		5/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0011421	PMID:29455859	PCS		1/5			C	HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0002205	PMID:29455859	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0001522	PMID:29455859	PCS		2/5			C	HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0000006	PMID:29455859	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0001744	PMID:29455859	PCS		4/4			P	HPO:probinson[2022-08-13]
OMIM:618042	Pulmonary alveolar proteinosis with hypogammaglobulinemia		HP:0001974	PMID:29455859	PCS		5/5			P	HPO:probinson[2022-08-13]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0002069	OMIM:300388	TAS					P	HPO:probinson[2012-07-20]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0007270	OMIM:300388	TAS					P	HPO:probinson[2009-02-17]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0100543	OMIM:300388	TAS					P	HPO:probinson[2012-07-20]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0000750	OMIM:300388	TAS					P	HPO:probinson[2012-07-20]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0001260	OMIM:300388	TAS					P	HPO:probinson[2012-07-20]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0007024	OMIM:300388	TAS					P	HPO:probinson[2009-02-17]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0010522	OMIM:300388	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0001423	OMIM:300388	TAS					I	HPO:probinson[2009-02-17]
OMIM:300388	Polymicrogyria, bilateral perisylvian		HP:0002126	OMIM:300388	TAS					P	HPO:probinson[2009-02-17]
OMIM:140700	Heinz body anemias		HP:0020082	OMIM:140700	IEA					P	HPO:skoehler[2019-09-07]
OMIM:140700	Heinz body anemias		HP:0005511	OMIM:140700	IEA					P	HPO:skoehler[2015-01-21]
OMIM:140700	Heinz body anemias		HP:0000006	OMIM:140700	IEA					I	HPO:iea[2009-02-17]
OMIM:140700	Heinz body anemias		HP:0001930	OMIM:140700	IEA					P	HPO:iea[2009-02-17]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0003510	PMID:30478443	PCS		3/3			P	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0004325	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0000286	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0006009	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0000252	PMID:30478443	PCS		3/3		HP:0012828	P	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0000486	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0000750	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0001230	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0001263	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0010049	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0008070	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0000337	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0000878	PMID:30478443	PCS		1/3			P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0001511	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0000006	PMID:30478443	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618724	Heyn-Sproul-Jackson syndrome		HP:0009803	PMID:30478443	PCS					P	HPO:probinson[2020-05-11]
OMIM:144200	Palmoplantar keratoderma, epidermolytic		HP:0003212	OMIM:144200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:144200	Palmoplantar keratoderma, epidermolytic		HP:0000972	OMIM:144200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:144200	Palmoplantar keratoderma, epidermolytic		HP:0007556	OMIM:144200	TAS					P	HP:probinson[2019-03-02]
OMIM:144200	Palmoplantar keratoderma, epidermolytic		HP:0000006	PMID:12192490	PCS					I	HPO:skoehler[2009-02-17];HP:probinson[2019-03-02]
OMIM:144200	Palmoplantar keratoderma, epidermolytic		HP:0007559	PMID:12192490	PCS					P	HPO:skoehler[2009-02-17];HP:probinson[2019-03-02]
OMIM:144200	Palmoplantar keratoderma, epidermolytic		HP:0010765	OMIM:144200	TAS					P	HP:probinson[2019-03-02]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0002465	PMID:17618476	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000750	PMID:17618476	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000486	PMID:17618476	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000540	PMID:17618476	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0001382	PMID:17618476	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0001263	PMID:17618476	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0010807	PMID:17618476	PCS		6/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0003593	PMID:17618476	PCS					C	HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000709	PMID:17618476	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000646	PMID:17618476	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000007	PMID:21035105	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0430028	PMID:17618476	PCS		6/7			P	HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000678	PMID:17618476	PCS		6/7			P	HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000736	PMID:17618476	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000505	PMID:17618476	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-06]
OMIM:613671	Impaired intellectual development, anterior maxillary protrusion, and strabismus		HP:0000565	PMID:21035105	PCS		6/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-06]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002421	PMID:22526350	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000340	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0003577	PMID:22526350	PCS		2/2			C	HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002123	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002365	PMID:22526350	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0004322	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0001274	PMID:22526350	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0010541	PMID:22526350	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000817	PMID:22526350	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002119	PMID:22526350	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0001302	OMIM:605013	TAS					P	HPO:skoehler[2014-04-13]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0001347	PMID:22526350	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0003700	PMID:22526350	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0003202	OMIM:605013	TAS					P	HPO:skoehler[2014-04-13]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000252	PMID:22526350	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002510	PMID:22526350	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0001762	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0001321	PMID:22526350	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0001263	OMIM:605013	TAS				HP:0012829	P	HPO:skoehler[2014-04-13]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0012736	OMIM:605013	TAS					P	HPO:skoehler[2015-12-30]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002828	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000426	PMID:22526350	PCS		2/2			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000007	PMID:22526350	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000400	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002305	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000520	OMIM:605013	TAS					P	HPO:skoehler[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0001510	PMID:22526350	PCS		2/2			P	HPO:probinson[2022-08-07]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0002324	OMIM:605013	IEA					P	HPO:iea[2009-02-17]
OMIM:605013	MICROHYDRANENCEPHALY		HP:0000742	PMID:22526350	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-07]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0002421	PMID:26637978	PCS		8/8			P	HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0000483	OMIM:616721	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0002059	PMID:26637978	PCS		1/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0003577	PMID:26637978	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001363	OMIM:616721	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0000365	OMIM:616721	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0002540	PMID:26637978	PCS		6/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0000486	PMID:26637978	PCS		7/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0004322	PMID:26637978	PCS		3/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001272	PMID:26637978	PCS		7/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001382	PMID:26637978	PCS		2/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001250	PMID:26637978	PCS		2/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001263	PMID:26637978	PCS				HP:0012829	P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001252	PMID:26637978	PCS		8/8		HP:0012829	P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0012707	PMID:26637978	PCS		1/2			P	HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0000639	OMIM:616721	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0002719	PMID:26637978	PCS		5/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0000938	PMID:26637978	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0000007	PMID:26637978	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0025336	PMID:26637978	PCS		8/8			P	HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001249	PMID:26637978	PCS		8/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0001347	PMID:26637978	PCS		2/8			P	HPO:probinson[2022-10-20]
OMIM:616721	Congenital disorder of glycosylation, type IIN		HP:0006855	PMID:26637978	PCS		7/7			P	HPO:probinson[2022-10-20]
OMIM:141350	Hemifacial hyperplasia with strabismus		HP:0000176	OMIM:141350	IEA					P	HPO:iea[2009-02-17]
OMIM:141350	Hemifacial hyperplasia with strabismus		HP:0000486	OMIM:141350	IEA					P	HPO:iea[2009-02-17]
OMIM:141350	Hemifacial hyperplasia with strabismus		HP:0005323	OMIM:141350	IEA					P	HPO:iea[2009-02-17]
OMIM:141350	Hemifacial hyperplasia with strabismus		HP:0000646	OMIM:141350	IEA					P	HPO:iea[2009-02-17]
OMIM:141350	Hemifacial hyperplasia with strabismus		HP:0000006	OMIM:141350	IEA					I	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0002684	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0004322	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0001250	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000581	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0001252	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0001290	OMIM:301900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000280	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0008094	OMIM:301900	TAS					P	HPO:probinson[2012-06-08]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000639	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0006110	OMIM:301900	TAS					P	HPO:probinson[2012-06-09]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0008478	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000336	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0006118	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000054	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000252	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0002353	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0002650	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000771	OMIM:301900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000490	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0045025	OMIM:301900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0001182	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0001419	OMIM:301900	IEA					I	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0002808	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000508	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000505	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000823	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0008445	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0008687	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000400	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0000028	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0001513	OMIM:301900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301900	Borjeson-Forssman-Lehmann syndrome		HP:0001831	OMIM:301900	IEA					P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0002059	OMIM:600143	IEA					P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0003621	PMID:15024724	PCS		5/6			C	HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0000750	OMIM:600143	IEA					P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0002353	OMIM:600143	IEA					P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0002376	PMID:15024724	PCS		6/6			P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0001250	PMID:15024724	PCS		6/6			P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0001272	OMIM:600143	IEA					P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0002074	OMIM:600143	IEA					P	HPO:iea[2009-02-17]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0001251	PMID:15024724	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0000529	PMID:15024724	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0011463	PMID:15024724	PCS		1/6			C	HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0000007	PMID:15024724	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0003208	PMID:15024724	PCS		6/6			P	HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0002505	PMID:15024724	PCS	HP:0003621	3/3			P	HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0001336	PMID:15024724	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:600143	Ceroid lipofuscinosis, neuronal, 8		HP:0003205	OMIM:600143	IEA					P	HPO:iea[2009-02-17]
OMIM:188150	Thumb deformity and alopecia		HP:0001596	OMIM:188150	IEA					P	HPO:iea[2009-02-17]
OMIM:188150	Thumb deformity and alopecia		HP:0004322	OMIM:188150	IEA					P	HPO:iea[2009-02-17]
OMIM:188150	Thumb deformity and alopecia		HP:0007450	OMIM:188150	IEA					P	HPO:iea[2009-02-17]
OMIM:188150	Thumb deformity and alopecia		HP:0009778	OMIM:188150	IEA					P	HPO:iea[2009-02-17]
OMIM:188150	Thumb deformity and alopecia		HP:0000006	OMIM:188150	IEA					I	HPO:iea[2009-02-17]
OMIM:188150	Thumb deformity and alopecia		HP:0001249	OMIM:188150	IEA					P	HPO:iea[2009-02-17]
OMIM:188150	Thumb deformity and alopecia		HP:0006315	OMIM:188150	IEA					P	HPO:iea[2009-02-17]
OMIM:613659	Gastric cancer, somatic		HP:0001442	OMIM:613659	TAS					I	HPO:skoehler[2013-02-23]
OMIM:613659	Gastric cancer, somatic		HP:0410067	PMID:2311216	PCS					P	HPO:NicoleVasilevsky[2018-02-23]
OMIM:613659	Gastric cancer, somatic		HP:0012126	OMIM:613659	TAS					P	HPO:skoehler[2013-01-09]
OMIM:613881	Cardiomyopathy, dilated, 1HH		HP:0003596	PMID:21353195	PCS		13/23			C	HPO:probinson[2022-07-04]
OMIM:613881	Cardiomyopathy, dilated, 1HH		HP:0003584	PMID:21353195	PCS		1/23			C	HPO:probinson[2022-07-04]
OMIM:613881	Cardiomyopathy, dilated, 1HH		HP:0011462	PMID:21353195	PCS		9/23			C	HPO:probinson[2022-07-04]
OMIM:613881	Cardiomyopathy, dilated, 1HH		HP:0001635	PMID:21353195	PCS		10/23			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613881	Cardiomyopathy, dilated, 1HH		HP:0033755	PMID:21353195	PCS		12/18			P	HPO:probinson[2022-07-04]
OMIM:613881	Cardiomyopathy, dilated, 1HH		HP:0000006	PMID:21353195	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:613881	Cardiomyopathy, dilated, 1HH		HP:0001644	PMID:21353195	PCS		18/22			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-07-04]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0001298	PMID:23599390	PCS		2/2		HP:0003676	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0025430	PMID:23599390	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0003577	PMID:23599390	PCS		2/2			C	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0002089	PMID:23599390	PCS		2/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0001321	PMID:23599390	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0001250	PMID:23599390	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0011925	PMID:23599390	PCS		2/2			P	HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0000639	PMID:23599390	PCS		2/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0000737	PMID:23599390	PCS		2/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0000007	PMID:23599390	PCS					I	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0003811	PMID:23599390	PCS		2/2			C	HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0002104	PMID:23599390	PCS		2/2			P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-11]
OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4		HP:0003535	PMID:23599390	PCS		0/2			P	HPO:probinson[2023-03-11]
OMIM:145650	Thyroid hormone resistance, selective pituitary		HP:0000836	OMIM:145650	TAS					P	HPO:probinson[2009-02-17]
OMIM:145650	Thyroid hormone resistance, selective pituitary		HP:0002925	OMIM:145650	TAS					P	HPO:probinson[2013-03-10]
OMIM:145650	Thyroid hormone resistance, selective pituitary		HP:0000006	OMIM:145650	TAS					I	HPO:probinson[2009-02-17]
OMIM:145650	Thyroid hormone resistance, selective pituitary		HP:0002930	OMIM:145650	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0002223	PMID:16525032	PCS		8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-10]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0000561	PMID:16525032	PCS		8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-10]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0000164	PMID:16525032	PCS		0/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-16]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0003577	PMID:16525032	PCS		8/8			C	HPO:probinson[2024-03-10]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0001596	PMID:16525032	PCS	HP:0003577	8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-10]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0002299	OMIM:602032	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0002231	PMID:16525032	PCS		8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-16]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0008394	PMID:16525032	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-16]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0001806	OMIM:602032	IEA					P	HPO:iea[2009-02-17]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0000007	PMID:19865094	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2020-07-19]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0008404	PMID:16525032	PCS	HP:0003577	8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-10]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0000972	PMID:16525032	PCS		0/8			P	HPO:probinson[2024-03-16]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0000971	PMID:16525032	PCS		0/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-10]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0001249	PMID:16525032	PCS		0/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-03-10]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0003777	OMIM:602032	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602032	Ectodermal dysplasia 4, hair/nail type		HP:0004524	OMIM:602032	IEA					P	HPO:iea[2009-02-17]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0003774	PMID:21540551	PCS	HP:0003621	8/12			P	HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0003621	PMID:21540551	PCS		2/12			C	HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0001250	PMID:21540551	PCS		2/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0000097	PMID:21540551	PCS		7/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0003593	PMID:21540551	PCS		5/12			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0000093	PMID:21540551	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0012588	PMID:21540551	PCS		11/12			P	HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0000407	PMID:21540551	PCS		10/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0011463	PMID:21540551	PCS		5/12			C	HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0000007	PMID:21540551	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0001967	PMID:21540551	PCS		1/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0000787	PMID:21540551	PCS		1/12			P	HPO:probinson[2022-11-26]
OMIM:614650	Coenzyme Q10 deficiency, primary, 6		HP:0003678	PMID:21540551	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-26]
OMIM:600625	Orofacial cleft 11		HP:0000175	PMID:19249007	PCS					P	HPO:probinson[2020-07-24]
OMIM:600625	Orofacial cleft 11		HP:0410030	PMID:19249007	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-07-24]
OMIM:600625	Orofacial cleft 11		HP:0010982	PMID:19249007	PCS					I	HP:probinson[2018-09-16]
OMIM:619374	Immunodeficiency 81		HP:0003203	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0030388	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0001890	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0031402	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0031545	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0012177	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0002719	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0008320	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0000007	PMID:33231617	PCS					I	HPO:probinson[2021-07-12];HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0000967	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0000988	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0100838	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0040238	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0025615	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:619374	Immunodeficiency 81		HP:0002721	PMID:33231617	PCS		1/1			P	HPO:probinson[2021-07-12]
OMIM:600631	Enuresis, nocturnal, 1		HP:0000006	OMIM:600631	TAS					I	HPO:skoehler[2009-02-17]
OMIM:600631	Enuresis, nocturnal, 1		HP:0010677	OMIM:600631	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610422	Alopecia-intellectual disability syndrome 2		HP:0002289	OMIM:610422	IEA					P	HPO:iea[2009-02-17]
OMIM:610422	Alopecia-intellectual disability syndrome 2		HP:0000007	OMIM:610422	IEA					I	HPO:iea[2009-02-17]
OMIM:610422	Alopecia-intellectual disability syndrome 2		HP:0001249	OMIM:610422	IEA					P	HPO:iea[2009-02-17]
OMIM:606240	Thyroid cancer, nonmedullary, 3		HP:0040198	OMIM:606240	TAS					P	HPO:skoehler[2015-10-11]
OMIM:606240	Thyroid cancer, nonmedullary, 3		HP:0000006	OMIM:606240	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616053	Spinocerebellar ataxia 40		HP:0002168	PMID:25062847	PCS		2/2			P	HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0006879	PMID:25062847	PCS		2/2			P	HPO:skoehler[2015-01-04]
OMIM:616053	Spinocerebellar ataxia 40		HP:0002136	PMID:25062847	PCS		1/2			P	HPO:skoehler[2015-01-04]
OMIM:616053	Spinocerebellar ataxia 40		HP:0003596	PMID:25062847	PCS		2/2			C	HPO:probinson[2023-03-27];HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0001310	PMID:25062847	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:616053	Spinocerebellar ataxia 40		HP:0002066	PMID:25062847	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0001260	PMID:25062847	PCS		1/2			P	HPO:skoehler[2015-01-04]
OMIM:616053	Spinocerebellar ataxia 40		HP:0002075	PMID:25062847	PCS		1/2			P	HPO:skoehler[2015-01-04]
OMIM:616053	Spinocerebellar ataxia 40		HP:0001251	PMID:25062847	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0002080	PMID:25062847	PCS		1/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0011448	PMID:25062847	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0002317	PMID:25062847	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0001337	PMID:25062847	PCS		1/2			P	HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0002313	PMID:25062847	PCS		1/2			P	HPO:skoehler[2015-01-04]
OMIM:616053	Spinocerebellar ataxia 40		HP:0003677	PMID:25062847	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0000006	PMID:25062847	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-27]
OMIM:616053	Spinocerebellar ataxia 40		HP:0001347	PMID:25062847	PCS		1/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-03-27]
OMIM:619360	Angioedema, hereditary, 4		HP:0100665	PMID:28795768	IEA				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619360	Angioedema, hereditary, 4		HP:0000282	PMID:28795768	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619360	Angioedema, hereditary, 4		HP:0011462	PMID:28795768	PCS					C	HPO:probinson[2021-07-13]
OMIM:619360	Angioedema, hereditary, 4		HP:0031244	PMID:28795768	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619360	Angioedema, hereditary, 4		HP:0012027	PMID:28795768	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619360	Angioedema, hereditary, 4		HP:0000006	PMID:28795768	PCS					I	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:185460	Sulfhemoglobinemia, congenital		HP:0001871	OMIM:185460	IEA					P	HPO:iea[2009-02-17]
OMIM:185460	Sulfhemoglobinemia, congenital		HP:0000961	OMIM:185460	IEA					P	HPO:skoehler[2010-06-20]
OMIM:185460	Sulfhemoglobinemia, congenital		HP:0000006	OMIM:185460	IEA					I	HPO:iea[2009-02-17]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0000848	PMID:33811157	PCS		7/7			P	HPO:probinson[2021-07-07]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0000859	PMID:33811157	PCS		5/7			P	HPO:probinson[2021-07-07]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0001250	PMID:33811157	PCS		0/8			P	HPO:probinson[2021-07-07]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0000407	PMID:33811157	PCS		8/8			P	HPO:probinson[2021-07-07]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0001251	PMID:33811157	PCS		0/8			P	HPO:probinson[2021-07-07]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0000007	PMID:33811157	PCS					I	HPO:probinson[2021-07-07];HPO:probinson[2021-07-07]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0000127	PMID:33811157	PCS		6/8			P	HPO:probinson[2021-07-07]
OMIM:619406	Hypokalemic tubulopathy and deafness		HP:0001941	PMID:33811157	PCS		7/8			P	HPO:probinson[2021-07-07]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0008947	PMID:31668703	PCS		14/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0002540	PMID:31668703	PCS		12/15			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001250	PMID:31668703	PCS		5/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001270	PMID:31668703	PCS	HP:0003593	16/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0012444	PMID:31668703	PCS		4/8		HP:0012825	P	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000639	PMID:31668703	PCS		1/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000733	PMID:31668703	PCS					P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0002714	PMID:31668703	PCS		2/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000752	PMID:31668703	PCS		7/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001324	PMID:31668703	PCS		9/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001249	PMID:31668703	PCS					P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0003763	PMID:31668703	PCS		7/15			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000252	PMID:31668703	PCS		5/14			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000750	PMID:31668703	PCS		15/15			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001344	PMID:31668703	PCS		11/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0002353	PMID:31668703	PCS		6/10			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0002376	PMID:31668703	PCS		14/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001263	PMID:31668703	PCS		16/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000749	PMID:31668703	PCS		13/15			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000729	PMID:31668703	PCS		13/15			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000007	PMID:31668703	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000601	PMID:31668703	PCS		3/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0100716	PMID:31668703	PCS		7/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0002307	PMID:31668703	PCS		3/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000565	PMID:31668703	PCS		1/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0002007	PMID:31668703	PCS		2/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001257	PMID:31668703	PCS		6/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0001337	PMID:31668703	PCS		2/16			P	HPO:probinson[2020-05-11]
OMIM:618718	Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia		HP:0000369	PMID:31668703	PCS		2/16			P	HPO:probinson[2020-05-11]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0001298	PMID:23596069	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0003577	PMID:23596069	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0000252	PMID:23596069	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0001250	PMID:23596069	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0011924	PMID:23596069	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0001252	PMID:23596069	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0002092	PMID:23596069	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0011923	PMID:23596069	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0009141	PMID:23596069	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0001508	PMID:23596069	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0000007	PMID:23596069	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0001635	PMID:23596069	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0008347	PMID:23596069	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0001511	PMID:23596069	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:616045	Combined oxidative phosphorylation deficiency 22		HP:0003348	PMID:23596069	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-05]
OMIM:619376	Faundes-Banka syndrome		HP:0000286	PMID:33547280	PCS		5/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0003577	PMID:33547280	PCS		4/7			C	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0005830	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0030674	PMID:33547280	PCS		3/7			C	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001791	PMID:33547280	PCS	HP:0011461	1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001252	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0002020	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001508	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0008551	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0012450	PMID:33547280	PCS		2/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000316	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001800	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0008872	PMID:33547280	PCS		4/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000414	PMID:33547280	PCS		4/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000219	PMID:33547280	PCS		4/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000637	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000378	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001763	PMID:33547280	PCS		3/7			P	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0008439	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0002015	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000494	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000175	PMID:33547280	PCS	HP:0003577	1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000430	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001382	PMID:33547280	PCS		3/6			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000490	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0400004	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0011229	PMID:33547280	PCS		5/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0010314	PMID:33547280	PCS		1/4			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0011451	PMID:33547280	PCS	HP:0003577	3/5			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000729	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0002209	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001319	PMID:33547280	PCS	HP:0003623	2/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0007697	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000405	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000823	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001357	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0001511	PMID:33547280	PCS	HP:0011461	3/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0002007	PMID:33547280	PCS		1/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000347	PMID:33547280	PCS		5/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000369	PMID:33547280	PCS		3/7			P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000028	PMID:33547280	PCS		1/3	MALE		P	HPO:probinson[2021-08-20]
OMIM:619376	Faundes-Banka syndrome		HP:0000006	PMID:33547280	PCS					I	HPO:probinson[2021-08-20];HPO:probinson[2021-08-20]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000286	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0003159	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000750	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000431	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0001250	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0001263	OMIM:601539	TAS		20/20			P	HPO:skoehler[2019-02-22];HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0001395	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0001394	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0002240	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0001290	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0011800	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0010655	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000407	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000107	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000007	OMIM:601539	TAS					I	HPO:probinson[2013-01-09]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0001319	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000648	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000510	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0000444	OMIM:601539	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601539	Peroxisome biogenesis disorder 1B		HP:0002415	OMIM:601539	TAS					P	HPO:probinson[2013-02-24]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0004325	PMID:25210931	PCS		5/5			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0000486	PMID:25210931	PCS		3/6			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0004322	PMID:25210931	PCS		6/6			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0008064	PMID:25210931	PCS		6/6			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0000639	PMID:25210931	PCS		2/6			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0040189	PMID:25210931;PMID:27208707	PCS		7/7			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0000998	PMID:27208707	PCS		6/6			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0001217	PMID:27208707	PCS		0/1			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0001019	PMID:25210931	PCS	HP:0003577	6/6			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0000656	PMID:25210931;PMID:27208707	PCS		5/7			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0000989	PMID:25210931	PCS		2/6			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0000972	PMID:25210931	PCS		4/6			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0002557	PMID:25210931;PMID:27208707	PCS		6/7			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0007479	PMID:25210931	PCS	HP:0003577	4/6			P	HPO:probinson[2022-05-28]
OMIM:609165	Erythroderma, ichthyosiform, congenital reticular		HP:0000006	PMID:25210931	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-05-28]
OMIM:600627	Hypertryptophanemia		HP:0001377	OMIM:600627	IEA					P	HPO:iea[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0000486	OMIM:600627	IEA					P	HPO:iea[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0002761	OMIM:600627	IEA					P	HPO:iea[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:5200321	OMIM:600627	TAS					P	HPO:skoehler[2015-01-04]
OMIM:600627	Hypertryptophanemia		HP:0100490	OMIM:600627	TAS					P	HPO:probinson[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0025268	OMIM:600627	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600627	Hypertryptophanemia		HP:0003144	PMID:28285122	PCS		1/1			P	HPO:probinson[2023-04-18]
OMIM:600627	Hypertryptophanemia		HP:0001263	PMID:28285122	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-18]
OMIM:600627	Hypertryptophanemia		HP:0003361	OMIM:600627	TAS					P	HPO:probinson[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0001181	OMIM:600627	TAS					P	HPO:probinson[2013-08-12]
OMIM:600627	Hypertryptophanemia		HP:0000716	OMIM:600627	TAS					P	HPO:skoehler[2015-12-30]
OMIM:600627	Hypertryptophanemia		HP:0000407	OMIM:600627	TAS					P	HPO:skoehler[2015-12-30]
OMIM:600627	Hypertryptophanemia		HP:0000718	OMIM:600627	TAS					P	HPO:probinson[2013-08-12]
OMIM:600627	Hypertryptophanemia		HP:0000712	OMIM:600627	IEA					P	HPO:iea[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0000316	OMIM:600627	IEA					P	HPO:iea[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0000007	PMID:28285122	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-18]
OMIM:600627	Hypertryptophanemia		HP:0000505	OMIM:600627	TAS					P	HPO:probinson[2013-08-12]
OMIM:600627	Hypertryptophanemia		HP:0001763	OMIM:600627	TAS					P	HPO:probinson[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0000545	OMIM:600627	IEA					P	HPO:iea[2009-02-17]
OMIM:600627	Hypertryptophanemia		HP:0001249	PMID:28285122	PCS		0/1			P	HPO:probinson[2023-04-18]
OMIM:600627	Hypertryptophanemia		HP:0500134	PMID:28285122	PCS	HP:0003623	1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-04-18]
OMIM:600627	Hypertryptophanemia		HP:0003623	PMID:28285122	PCS		1/1			C	HPO:probinson[2023-04-18]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0000100	PMID:17186472	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0011968	PMID:17186472	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0002151	PMID:17186472	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0003073	PMID:17186472	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0032663	PMID:17186472	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0000093	PMID:17186472	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0034369	PMID:17186472	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0007183	PMID:17186472	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0000969	PMID:17186472	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0100704	PMID:17186472	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0000007	PMID:17186472	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0001319	PMID:17186472	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0007334	PMID:17186472	PCS		1/1			P	HPO:probinson[2023-02-17]
OMIM:614652	Coenzyme Q10 deficiency, primary, 3		HP:0003623	PMID:17186472	PCS		1/1			C	HPO:probinson[2023-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000286	PMID:21706002	PCS		1/7			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000486	PMID:21706002	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000243	PMID:21706002	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0004322	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001250	PMID:21706002	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001052	OMIM:605039	TAS					P	HPO:probinson[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001371	PMID:21706002	PCS		6/7			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000160	PMID:21706002	PCS		1/6			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001373	OMIM:605039	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001252	OMIM:605039;PMID:21706002	PCS		15/17			P	HPO:probinson[2022-08-27];HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0002020	OMIM:605039	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605039	Bohring-Opitz syndrome		HP:0006191	PMID:21706002	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0011220	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001845	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000316	PMID:21706002	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0006276	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000998	PMID:21706002	PCS		6/7			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000278	PMID:21706002	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001169	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000358	PMID:21706002	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001007	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0003049	OMIM:605039	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605039	Bohring-Opitz syndrome		HP:0000252	PMID:21706002	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0005026	OMIM:605039	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605039	Bohring-Opitz syndrome		HP:0002079	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0011968	PMID:21706002	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001263	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000294	PMID:21706002	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0011401	OMIM:605039	PCS					P	HPO:probinson[2012-03-12]
OMIM:605039	Bohring-Opitz syndrome		HP:0001182	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0003083	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0012385	OMIM:605039	TAS					P	HPO:skoehler[2013-10-22]
OMIM:605039	Bohring-Opitz syndrome		HP:0100337	PMID:21706002	PCS		2/7			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0100334	PMID:21706002	PCS		1/7			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000329	PMID:21706002	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000960	PMID:21706002	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000520	PMID:21706002	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000369	PMID:21706002	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000204	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000006	PMID:21706002	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000341	OMIM:605039	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000187	PMID:21706002	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000582	PMID:21706002	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0003577	PMID:21706002	PCS		7/7			C	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000189	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0002365	OMIM:605039	TAS					P	HPO:skoehler[2014-04-04]
OMIM:605039	Bohring-Opitz syndrome		HP:0000463	PMID:21706002	PCS		2/6			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001274	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0002282	OMIM:605039	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605039	Bohring-Opitz syndrome		HP:0001629	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001508	PMID:21706002	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0002719	PMID:21706002	PCS		4/6			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001305	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001869	OMIM:605039	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0006610	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0002558	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000973	PMID:21706002	PCS		2/7			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000076	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001561	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000431	PMID:21706002	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000276	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0005487	OMIM:605039	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0005280	PMID:21706002	PCS		2/6			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0100874	OMIM:605039	TAS					P	HPO:skoehler[2012-10-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0001159	PMID:21706002	PCS		3/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001511	PMID:21706002	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000587	OMIM:605039	TAS					P	HPO:skoehler[2014-05-04]
OMIM:605039	Bohring-Opitz syndrome		HP:0001631	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0000545	PMID:21706002	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0000347	PMID:21706002	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0002566	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:605039	Bohring-Opitz syndrome		HP:0002643	PMID:21706002	PCS	HP:0003623	2/7			P	HPO:probinson[2022-08-27]
OMIM:605039	Bohring-Opitz syndrome		HP:0001831	OMIM:605039	IEA					P	HPO:iea[2009-02-17]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0003015	OMIM:269300	TAS					P	HPO:probinson[2012-05-07]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0001355	OMIM:269300	IEA					P	HPO:iea[2009-02-17]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0004322	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000260	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0003155	OMIM:269300	IEA					P	HPO:iea[2009-02-17]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0001090	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0011220	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000938	OMIM:269300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000678	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002857	OMIM:269300	TAS					P	HPO:probinson[2012-05-07]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000218	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000256	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0005622	OMIM:269300	IEA					P	HPO:iea[2009-02-17]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000494	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000670	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000695	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002650	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002694	OMIM:269300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:6001098	PMID:34484289	PCS					P	HPO:probinson[2024-12-14]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002970	OMIM:269300	TAS					P	HPO:probinson[2009-02-17]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002673	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000691	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000272	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000007	OMIM:269300	TAS					I	HPO:iea[2009-02-17]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002967	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002689	OMIM:269300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0002645	OMIM:269300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000369	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000303	OMIM:269300	TAS				HP:0012825	P	HPO:skoehler[2015-04-05]
OMIM:269300	Craniometadiaphyseal dysplasia		HP:0000885	OMIM:269300	TAS					P	HPO:skoehler[2015-04-05]
OMIM:614134	Stickler syndrome, type IV		HP:0000286	PMID:21421862	PCS		1/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0000483	PMID:16909383	PCS		4/4			P	HPO:probinson[2015-02-28]
OMIM:614134	Stickler syndrome, type IV		HP:0004322	PMID:21421862;PMID:16909383	PCS		13/13			P	HPO:probinson[2024-02-17];HPO:probinson[2015-02-28]
OMIM:614134	Stickler syndrome, type IV		HP:0003370	PMID:16909383	PCS		2/4			P	HPO:probinson[2015-02-28]
OMIM:614134	Stickler syndrome, type IV		HP:0010049	PMID:21421862	PCS		1/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0012368	PMID:16909383	PCS		4/4			P	HPO:probinson[2015-02-28]
OMIM:614134	Stickler syndrome, type IV		HP:0100864	PMID:21421862	PCS		2/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0000518	PMID:21421862	PCS		3/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0012371	PMID:21421862	PCS		1/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0012230	PMID:21421862	PCS		3/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0002812	PMID:21421862	PCS		2/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0002857	PMID:16909383	PCS		4/4			P	HPO:probinson[2015-02-28]
OMIM:614134	Stickler syndrome, type IV		HP:0002656	PMID:21421862;PMID:16909383	PCS		13/13			P	HPO:probinson[2013-08-10];HPO:probinson[2021-02-26];HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0200065	PMID:21421862	PCS		3/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0007964	PMID:16909383	PCS		4/4			P	HPO:probinson[2013-08-10];HPO:probinson[2021-02-26]
OMIM:614134	Stickler syndrome, type IV		HP:0001763	PMID:21421862	PCS		2/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0002650	PMID:21421862	PCS		1/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0001382	PMID:21421862	PCS		0/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0005041	PMID:16909383	PCS		2/4			P	HPO:probinson[2015-02-28]
OMIM:614134	Stickler syndrome, type IV		HP:0011003	PMID:21421862	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-21]
OMIM:614134	Stickler syndrome, type IV		HP:0006361	PMID:21421862	PCS		1/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0000407	PMID:21421862	PCS		6/6			P	HPO:probinson[2024-02-17];HPO:probinson[2013-08-10];HPO:probinson[2020-07-21]
OMIM:614134	Stickler syndrome, type IV		HP:0000926	PMID:16909383	PCS		1/4			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0000007	PMID:21421862	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-21]
OMIM:614134	Stickler syndrome, type IV		HP:0002945	PMID:21421862	PCS		1/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0002866	PMID:21421862	PCS		1/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0000545	PMID:21421862	PCS		3/3			P	HPO:probinson[2024-02-17]
OMIM:614134	Stickler syndrome, type IV		HP:0001611	PMID:21421862	PCS		2/3			P	HPO:probinson[2024-02-17]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000286	PMID:26365341	PCS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0010804	PMID:26365341	PCS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000486	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001377	PMID:26365341	PCS		1/1			P	HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0002980	OMIM:616723	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001498	PMID:26365341	PCS		5/5			P	HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0004322	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0003275	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0003196	PMID:26365341	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0003593	PMID:26365341	PCS		1/1			C	HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0010049	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001290	OMIM:616723	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001270	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0010585	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0100864	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0012471	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000938	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0008551	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001845	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000316	PMID:26365341	PCS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0002678	OMIM:616723	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001788	PMID:26365341	PCS		1/1			P	HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001249	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000252	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0001363	OMIM:616723	TAS		4/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0002650	PMID:26365341	PCS		5/5			P	HPO:probinson[2023-03-01];HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000750	PMID:26365341	PCS		1/1			P	HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0002750	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000470	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000272	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0005280	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0006461	OMIM:616723	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000729	PMID:26365341	PCS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000508	OMIM:616723	TAS				HP:0012825	P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000926	PMID:26365341	PCS		5/5			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000007	PMID:26365341	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0002944	OMIM:616723	TAS				HP:0012825	P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0002007	PMID:26365341	PCS		1/1			P	HPO:probinson[2023-03-01]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0000369	PMID:26365341	PCS		1/1			P	HPO:skoehler[2015-12-30]
OMIM:616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type		HP:0004689	PMID:26365341	PCS		5/5			P	HPO:probinson[2023-03-01]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003376	PMID:34459874	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003691	PMID:34459874	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0002061	PMID:34059824	PCS		6/11			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0033685	PMID:34059824	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003391	PMID:34459874	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0012473	PMID:34459874	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0033051	PMID:34459874	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0034045	PMID:34059824	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0011463	PMID:34059824;PMID:34459874	PCS		5/14			C	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0007340	PMID:36204986	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003307	PMID:34459874	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0001308	PMID:34459874	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0008954	PMID:36204986	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003700	PMID:34459874	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0001347	PMID:34459874	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003323	PMID:34059824	PCS		11/11			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0001265	PMID:34459874	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003621	PMID:34059824;PMID:36204986;PMID:34459874	PCS		7/15			C	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0003324	PMID:34459874	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0002650	PMID:34459874	PCS		1/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0001761	PMID:34459874	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0001288	PMID:36204986	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0002093	PMID:34059824	PCS		4/11			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0009050	PMID:36204986	PCS		1/1			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0025708	PMID:34059824	PCS		3/11			C	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0000726	PMID:34059824	PCS		0/11			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0033683	PMID:34459874	PCS		2/3			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0002505	PMID:34059824;PMID:34459874	PCS		10/14			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0030051	PMID:34059824	PCS		6/11			P	HPO:probinson[2023-07-09]
OMIM:620285	Amyotrophic lateral sclerosis 27, juvenile		HP:0000006	PMID:34059824	PCS					I	HPO:probinson[2023-07-09]
OMIM:193200	Vitiligo-associated multiple autoimmune disease susceptibility 6		HP:0001045	OMIM:193200	IEA					P	HPO:iea[2009-02-17]
OMIM:193200	Vitiligo-associated multiple autoimmune disease susceptibility 6		HP:0003764	OMIM:193200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:193200	Vitiligo-associated multiple autoimmune disease susceptibility 6		HP:0000007	OMIM:193200	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:600155	Hirschsprung disease, susceptibility to, 2		HP:0003577	PMID:8001158	PCS					C	HPO:probinson[2022-10-24]
OMIM:600155	Hirschsprung disease, susceptibility to, 2		HP:0002251	PMID:8001158	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:600155	Hirschsprung disease, susceptibility to, 2		HP:0000006	PMID:8001158	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-24]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000122	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001250	OMIM:616737	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001251	PMID:26708094	PCS		1/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001290	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0045075	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000319	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0011220	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000316	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001845	OMIM:616737	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0009623	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001643	PMID:26708094	PCS	HP:0011463	1/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001004	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001642	OMIM:616737	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000358	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001249	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002553	PMID:26708094	PCS		2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000253	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000494	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0003764	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001344	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002079	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001263	PMID:26708094	PCS		2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0011800	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001182	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0012385	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000407	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000689	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000766	OMIM:616737	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000648	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000322	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000047	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000369	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002500	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000006	OMIM:616737	IEA					I	HPO:skoehler[2019-04-18]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000126	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000687	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000341	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001671	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000582	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000343	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000023	PMID:26708094	PCS	HP:0011463	HP:0040283			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001272	PMID:26708094	PCS		1/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002120	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0011877	PMID:26708094	PCS		2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002719	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000414	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002518	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000219	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002119	PMID:26708094	PCS		2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002714	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0030084	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000454	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000577	PMID:26708094	PCS	HP:0011463	2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000154	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000431	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002650	OMIM:616737	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001321	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000708	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000508	PMID:26708094	IEA		2/2		HP:0012825	P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001999	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0007655	PMID:26708094	PCS		2/2			P	HPO:probinson[2017-05-28]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000664	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0001873	OMIM:616737	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000465	OMIM:616737	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0000028	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616737	Takenouchi-Kosaki syndrome		HP:0002721	OMIM:616737	IEA					P	HPO:skoehler[2018-10-08]
OMIM:117100	Centralopathic epilepsy		HP:0007334	OMIM:117100	TAS					P	HPO:probinson[2009-02-17]
OMIM:117100	Centralopathic epilepsy		HP:0003745	OMIM:117100	TAS					I	HPO:probinson[2014-01-04]
OMIM:117100	Centralopathic epilepsy		HP:0031951	OMIM:117100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:117100	Centralopathic epilepsy		HP:0007359	OMIM:117100	TAS					P	HPO:probinson[2013-12-15]
OMIM:117100	Centralopathic epilepsy		HP:0012557	OMIM:117100	TAS					P	HPO:probinson[2014-01-04]
OMIM:612551	Focal segmental glomerulosclerosis 4, susceptibility to		HP:0003774	PMID:20647424	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-08-10]
OMIM:612551	Focal segmental glomerulosclerosis 4, susceptibility to		HP:0000097	PMID:20647424	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2022-08-10]
OMIM:612551	Focal segmental glomerulosclerosis 4, susceptibility to		HP:0010982	PMID:20647424	PCS					I	HPO:skoehler[2013-03-12];HPO:probinson[2022-08-10]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0002465	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001792	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0011918	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001596	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0025267	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001808	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0000718	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0009886	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001688	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001864	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0003102	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0002376	PMID:31125343	PCS	HP:0011463	1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001382	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001260	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001263	PMID:31125343	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0000691	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0012514	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0004691	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0012378	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0005180	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0100710	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0032152	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0000007	PMID:31125343	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001954	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0000403	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0004704	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0004428	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001357	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0001653	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0003777	PMID:31125343	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0005338	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:261990	Abnormal hair, joint laxity, and developmental delay		HP:0004689	PMID:31125343	PCS		1/1			P	HPO:probinson[2021-06-01]
OMIM:614120	Hydrolethalus syndrome 2		HP:0000175	PMID:21552264	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0002323	PMID:21552264	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0001162	PMID:21552264	PCS		3/4			P	HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0001274	PMID:21552264	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0011461	PMID:21552264	PCS		4/4			C	HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0000007	PMID:21552264	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0000238	PMID:21552264	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0002419	PMID:21552264	PCS		1/1			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0002119	PMID:21552264	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0001830	PMID:21552264	PCS		2/4			P	HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0001841	PMID:21552264	PCS		3/4			P	HPO:probinson[2022-03-27]
OMIM:614120	Hydrolethalus syndrome 2		HP:0000347	PMID:21552264	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0000486	OMIM:113400	IEA					P	HPO:iea[2009-02-17]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0001156	OMIM:113400	TAS					P	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0000639	OMIM:113400	IEA					P	HPO:iea[2009-02-17]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0001251	OMIM:113400	IEA					P	HPO:iea[2009-02-17]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0010049	OMIM:113400	TAS					P	HPO:iea[2009-02-17]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0001249	OMIM:113400	IEA					P	HPO:iea[2009-02-17]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0000006	OMIM:113400	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:113400	Brachydactyly-Nystagmus-Cerebellar ataxia		HP:0010743	OMIM:113400	TAS					P	HPO:iea[2012-07-19]
OMIM:612237	Chondrosarcoma, extraskeletal myxoid		HP:0001442	OMIM:612237	TAS					I	HPO:probinson[2013-06-02]
OMIM:612237	Chondrosarcoma, extraskeletal myxoid		HP:0006765	OMIM:612237	TAS					P	HPO:probinson[2013-06-02]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0031956	PMID:21981844	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0003563	PMID:21981844;PMID:1939657	PCS		4/4			P	HPO:probinson[2022-09-22];HPO:probinson[2022-09-22];HPO:skoehler[2014-01-28];HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0002155	PMID:1939657	PCS		0/1			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0003233	PMID:21981844	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0003146	PMID:21981844	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0001251	OMIM:615558	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0003593	PMID:21981844	PCS		1/1			C	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0002570	PMID:21981844	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0031964	PMID:21981844	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0100513	PMID:21981844	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0001927	PMID:21981844	PCS		3/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0004905	PMID:21981844	PCS		3/3			P	HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0000546	OMIM:615558	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0000007	PMID:1939657	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0000510	PMID:21981844	PCS		0/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-09-22]
OMIM:615558	Hypobetalipoproteinemia, familial, 1		HP:0001315	OMIM:615558	TAS					P	HPO:skoehler[2014-01-28]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000252	PMID:24748105	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000340	PMID:24748105	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001773	PMID:24748105	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001321	PMID:24748105	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0004322	PMID:24748105	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001263	PMID:24748105	PCS		2/2			P	HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000639	PMID:24748105	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001607	PMID:24748105	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001518	PMID:24748105	PCS		2/2			P	HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0011451	PMID:24748105	PCS		1/1			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0032792	PMID:24748105	PCS	HP:0003593	1/2			P	HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0011461	PMID:24748105	PCS		2/2			C	HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000448	PMID:24748105	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000007	PMID:24748105	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001338	PMID:24748105	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001723	PMID:24748105	PCS	HP:0003577	1/2			P	HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0004979	PMID:24748105	PCS	HP:0003577	1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0001511	PMID:24748105	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0200055	PMID:24748105	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000400	PMID:24748105	PCS		1/2			P	HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000311	PMID:24748105	PCS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0000347	PMID:24748105	PCS	HP:0003593	1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-03-26]
OMIM:616051	Microcephaly 13, primary, autosomal recessive		HP:0009879	PMID:24748105	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0001561	PMID:28292896	PCS	HP:0011461	1/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0004388	PMID:28292896	PCS		1/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0010956	PMID:28292896	PCS	HP:0034198	1/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0000072	PMID:28292896	PCS		1/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0034198	PMID:28292896	PCS		1/1			C	HPO:probinson[2024-03-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0100806	PMID:28292896	PCS		1/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0000007	PMID:28292896	PCS					I	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0001627	PMID:28292896	PCS		0/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16];HPO:probinson[2024-03-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0003270	PMID:28292896	PCS		1/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0003811	PMID:28292896	PCS		1/1			C	HPO:probinson[2021-08-16]
OMIM:619362	Megacystis-microcolon-intestinal hypoperistalsis syndrome 3		HP:0000126	PMID:28292896	PCS		1/1			P	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:606242	Kondoh syndrome		HP:0001177	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0000252	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0001220	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0000343	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0000574	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0001047	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0004322	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0008070	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0006380	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0000508	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0000349	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0001999	OMIM:606242	IEA					P	HPO:skoehler[2015-01-19]
OMIM:606242	Kondoh syndrome		HP:0000007	OMIM:606242	IEA					I	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0000447	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0000219	OMIM:606242	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0001511	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:606242	Kondoh syndrome		HP:0001249	OMIM:606242	IEA					P	HPO:iea[2009-02-17]
OMIM:610420	Preauricular tag, isolated, autosomal dominant, 1		HP:0000384	OMIM:610420	TAS					P	HPO:iea[2009-02-17]
OMIM:610420	Preauricular tag, isolated, autosomal dominant, 1		HP:0003577	OMIM:610420	TAS					C	HPO:probinson[2022-07-02]
OMIM:610420	Preauricular tag, isolated, autosomal dominant, 1		HP:0000006	OMIM:610420	TAS					I	HPO:iea[2009-02-17]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0004313	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0002155	PMID:19804848	PCS					P	HPO:probinson[2013-06-02]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0002583	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0003593	PMID:19804848	IEA		8/13			C	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0003281	PMID:19804848	PCS					P	HPO:probinson[2013-06-02]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0011108	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0012177	PMID:19804848	PCS					P	HPO:probinson[2013-06-02]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0012156	PMID:19804848	PCS					P	HPO:probinson[2013-06-02]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0001903	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0011463	PMID:29776323;PMID:19804848	PCS		6/14			C	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0008573	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0000007	PMID:19804848	PCS					I	HPO:probinson[2013-06-02]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0001954	PMID:19804848	PCS					P	HPO:probinson[2013-06-02]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0006530	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0002716	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0001945	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0002788	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0001433	PMID:19804848	PCS					P	HPO:probinson[2013-06-02]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0001873	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:613101	Hemophagocytic lymphohistiocytosis, familial, 5		HP:0001744	PMID:29776323	PCS		1/1			P	HPO:probinson[2020-11-25]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001596	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0003493	PMID:35477763	PCS		3/3			P	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0025300	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0000739	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001888	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001945	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001423	PMID:35477763	PCS					I	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0002315	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0003621	PMID:35477763	PCS		2/3			C	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001882	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0000155	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0005421	PMID:35477763	PCS		2/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0030880	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0002072	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0045042	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0012486	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0100653	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0025708	PMID:35477763	PCS		1/3			C	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0002829	PMID:35477763	PCS		2/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0033342	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0100735	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001954	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0002725	PMID:35477763	PCS		2/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001973	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001873	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:301080	Systemic lupus erythematosus 17		HP:0001653	PMID:35477763	PCS		1/3			P	HPO:probinson[2022-07-11]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0000662	PMID:24026677	PCS		1/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0003596	PMID:24026677	PCS		3/9			C	HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0011462	PMID:24026677	PCS		6/9			C	HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0000613	PMID:24026677	PCS		9/9		HP:0012825	P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0007663	PMID:24026677	PCS		9/9			P	HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0000603	PMID:24026677	PCS		8/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0000543	PMID:24026677	PCS		9/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0000006	PMID:24026677	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-26]
OMIM:616079	Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities		HP:0000556	PMID:24026677	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-09-26]
OMIM:607174	Meningioma, familial, susceptibility to		HP:0003581	OMIM:607174	TAS					C	HPO:skoehler[2013-07-17]
OMIM:607174	Meningioma, familial, susceptibility to		HP:0003829	OMIM:607174	TAS					I	HPO:skoehler[2013-07-17]
OMIM:607174	Meningioma, familial, susceptibility to		HP:0002858	OMIM:607174	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607174	Meningioma, familial, susceptibility to		HP:0000006	OMIM:607174	TAS					I	HPO:skoehler[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0003774	OMIM:161900	TAS					P	HPO:skoehler[2013-01-21]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0003676	OMIM:161900	TAS					C	HPO:skoehler[2013-01-21]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0000123	OMIM:161900	IEA					P	HPO:iea[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0000083	OMIM:161900	IEA					P	HPO:iea[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0002907	OMIM:161900	IEA					P	HPO:iea[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0003581	OMIM:161900	IEA					C	HPO:iea[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0000822	OMIM:161900	IEA					P	HPO:iea[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0000093	OMIM:161900	IEA					P	HPO:iea[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0000006	OMIM:161900	IEA					I	HPO:iea[2009-02-17]
OMIM:161900	Renal failure, progressive, with hypertension		HP:0003259	OMIM:161900	TAS					P	HPO:skoehler[2013-01-21]
OMIM:136680	Frasier syndrome		HP:0003774	PMID:9398852	PCS	HP:0011462	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0000100	PMID:9398852	PCS	HP:0003621	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0000133	PMID:9398852	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0001442	OMIM:136680	TAS					I	HPO:iea[2009-02-17]
OMIM:136680	Frasier syndrome		HP:0000097	PMID:9398852	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0000093	PMID:9398852	PCS	HP:0011463	3/3			P	HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0000037	PMID:9398852	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0000006	PMID:9398852	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0000149	PMID:9398852	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:136680	Frasier syndrome		HP:0000786	PMID:9398852	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-05]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0031936	PMID:28585349	IEA		1/2			P	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0000194	PMID:28585349	PCS		1/2			P	HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0000319	PMID:28585349	PCS		1/2			P	HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0010808	PMID:28585349	PCS		1/2			P	HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0001290	PMID:28585349	PCS		1/2			P	HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0032794	PMID:28585349	PCS	HP:0011463	1/2			P	HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0002714	PMID:28585349	PCS		1/2			P	HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0000006	PMID:28585349	PCS					I	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0000303	PMID:28585349	PCS		1/2			P	HPO:probinson[2020-04-29]
OMIM:618732	Poirier-Bienvenu neurodevelopmental syndrome		HP:0001249	PMID:28585349	PCS		2/2			P	HPO:probinson[2020-04-29]
OMIM:221350	Deafness, congenital, with vitiligo and achalasia		HP:0001045	OMIM:221350	IEA					P	HPO:iea[2009-02-17]
OMIM:221350	Deafness, congenital, with vitiligo and achalasia		HP:0003202	OMIM:221350	IEA					P	HPO:iea[2009-02-17]
OMIM:221350	Deafness, congenital, with vitiligo and achalasia		HP:0000365	OMIM:221350	IEA					P	HPO:iea[2009-02-17]
OMIM:221350	Deafness, congenital, with vitiligo and achalasia		HP:0004322	OMIM:221350	IEA					P	HPO:iea[2009-02-17]
OMIM:221350	Deafness, congenital, with vitiligo and achalasia		HP:0002571	OMIM:221350	IEA					P	HPO:iea[2009-02-17]
OMIM:221350	Deafness, congenital, with vitiligo and achalasia		HP:0000007	OMIM:221350	IEA					I	HPO:iea[2009-02-17]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0003577	PMID:23522491;PMID:21055716;PMID:29200155	PCS		3/4			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0004322	PMID:21055716	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0000260	PMID:21055716	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0002240	PMID:23522491;PMID:21055716	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0031965	PMID:28265383	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0012132	PMID:23522491;PMID:21055716;PMID:29200155	PCS		3/4			P	HPO:skoehler[2013-06-13];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001903	PMID:28265383;PMID:23522491;PMID:21055716;PMID:29200155	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0011461	PMID:21055716	PCS		1/2			C	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001789	PMID:28265383;PMID:23522491;PMID:21055716	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0025435	PMID:28265383	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001923	PMID:28265383;PMID:23522491;PMID:21055716;PMID:29200155	PCS		13/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001824	PMID:28265383	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001744	PMID:23522491;PMID:21055716	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0020181	PMID:28265383	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0003621	PMID:28265383	PCS		1/1			C	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0000054	PMID:21055716	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0020062	PMID:28265383	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001981	PMID:23522491	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0011904	PMID:21055716;PMID:29200155	PCS		2/3			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0010972	PMID:21055716	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0031851	PMID:28265383	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0011273	PMID:28265383;PMID:23522491	PCS		2/2			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0008282	PMID:28265383;PMID:23522491	PCS		2/2			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0033281	PMID:23522491;PMID:21055716;PMID:29200155	PCS		3/4			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001639	PMID:21055716	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0002904	PMID:23522491;PMID:21055716	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001878	PMID:28265383;PMID:21055716	PCS		2/3			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0000821	PMID:21055716	PCS		1/2			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0002007	PMID:23522491	PCS		1/1			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0001433	PMID:28265383;PMID:29200155	PCS		2/2			P	HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0000047	PMID:21055716	PCS		1/1	MALE		P	HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0000006	PMID:21055716	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25]
OMIM:613673	Anemia, dyserythropoietic congenital, type IV		HP:0004447	PMID:28265383;PMID:23522491	PCS		2/2			P	HPO:probinson[2022-03-25]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0003577	PMID:12915478	PCS		15/15			C	HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0000007	PMID:12915478	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0000656	PMID:12915478	PCS		14/15			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0001217	PMID:12915478	PCS		1/15			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0001258	PMID:12915478	PCS		0/8			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0007479	PMID:12915478	PCS		15/15			P	HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0001433	PMID:12915478	PCS		0/8			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0000982	PMID:12915478	PCS		14/15			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11]
OMIM:601277	Ichthyosis, congenital, autosomal recessive 4A		HP:0001820	PMID:12915478	PCS		1/15			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-03-11]
OMIM:120790	Complement component 4, partial deficiency of		HP:0002725	OMIM:120790	IEA					P	HPO:iea[2009-02-17]
OMIM:120790	Complement component 4, partial deficiency of		HP:0000006	OMIM:120790	IEA					I	HPO:iea[2009-02-17]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000483	PMID:36368327	PCS		6/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000486	PMID:36368327	PCS		4/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000540	PMID:36368327	PCS		1/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0001250	PMID:36368327	PCS		3/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0001252	PMID:36368327	PCS		6/6			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0002020	PMID:36368327	PCS		1/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0003593	PMID:36368327	PCS		7/7			C	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0002061	PMID:36368327	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000639	PMID:36368327	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0012450	PMID:36368327	PCS		3/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000733	PMID:36368327	PCS		5/5			P	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000337	PMID:36368327	PCS		5/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000612	PMID:36368327	PCS	HP:0003577	1/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0008897	PMID:36368327	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0001423	PMID:36368327	PCS					I	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0001249	PMID:36368327	PCS		7/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000750	PMID:36368327	PCS		7/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0002376	PMID:36368327	PCS		2/8			P	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0001288	PMID:36368327	PCS		6/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0001263	PMID:36368327	PCS		7/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0011448	PMID:36368327	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0011471	PMID:36368327	PCS		1/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0000729	PMID:36368327	PCS		4/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0002904	PMID:36368327	PCS	HP:0003623	2/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0002205	PMID:36368327	PCS		2/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:301094	Neurodevelopmental disorder with gait disturbance, dysmorphic facies and behavioral abnormalities, X-linked		HP:0410018	PMID:36368327	PCS		3/7			P	HPO:probinson[2023-06-11];HPO:probinson[2023-06-11]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0001870	PMID:30643655	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0006801	PMID:30643655	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0001265	OMIM:613115	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0003477	PMID:30643655	PCS		4/4			P	HPO:skoehler[2010-06-20]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0003621	OMIM:613115	IEA					C	HPO:skoehler[2010-06-19]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0003676	PMID:30643655	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0001069	OMIM:613115	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0003487	PMID:30643655	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0031936	PMID:30643655	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0000020	OMIM:613115	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0001284	OMIM:613115	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0012407	PMID:30643655	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0007460	OMIM:613115	TAS					P	HP:probinson[2018-07-01];HP:probinson[2018-07-14]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0009771	PMID:30643655	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0011463	PMID:30643655	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0007340	PMID:30643655	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0006121	PMID:30643655	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0000007	PMID:30643655	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0002936	PMID:30643655	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0002359	PMID:30643655	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-23]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0001257	PMID:30643655	PCS		1/1			P	HPO:skoehler[2010-06-20]
OMIM:613115	Neuropathy, hereditary sensory and autonomic, type IIB		HP:0002754	OMIM:613115	IEA					P	HPO:skoehler[2010-06-19]
OMIM:614849	Immunodeficiency 132A		HP:0006846	PMID:20832341	PCS		1/1			P	HPO:probinson[2023-06-12]
OMIM:614849	Immunodeficiency 132A		HP:0011463	PMID:20832341	PCS		1/1			C	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:614849	Immunodeficiency 132A		HP:0012302	PMID:20832341	PCS	HP:0011463	1/1			P	HPO:probinson[2023-06-12]
OMIM:614849	Immunodeficiency 132A		HP:0000006	PMID:20832341	PCS					I	HPO:probinson[2023-06-12]
OMIM:210600	Seckel syndrome 1		HP:0000486	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001250	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001090	OMIM:210600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210600	Seckel syndrome 1		HP:0000954	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000678	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0003508	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0007048	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0008897	OMIM:210600	TAS					P	HPO:skoehler[2015-12-30]
OMIM:210600	Seckel syndrome 1		HP:0000878	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000752	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0006434	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001763	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000237	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001249	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000175	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000252	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000494	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0002750	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0003083	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0002827	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0006143	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000448	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000007	OMIM:210600	IEA					I	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000689	OMIM:210600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210600	Seckel syndrome 1		HP:0004209	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000444	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001852	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000047	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0002987	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000369	OMIM:210600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000324	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000340	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000581	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001592	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0010230	OMIM:210600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0006297	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000218	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001302	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000377	OMIM:210600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210600	Seckel syndrome 1		HP:0001320	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001883	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0002650	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0010583	OMIM:210600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210600	Seckel syndrome 1		HP:0006442	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0008665	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001511	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000028	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0000347	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:210600	Seckel syndrome 1		HP:0001876	OMIM:210600	IEA					P	HPO:iea[2009-02-17]
OMIM:614691	Cataract, autosomal recessive congenital 5		HP:0003577	PMID:22415731	PCS		3/3			C	HPO:probinson[2023-03-04]
OMIM:614691	Cataract, autosomal recessive congenital 5		HP:0000519	OMIM:614691	TAS	HP:0003577	3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:614691	Cataract, autosomal recessive congenital 5		HP:0000007	PMID:22415731	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-04]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0033150	PMID:32273475	PCS	HP:0003593	1/1			P	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0012311	PMID:32273475	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0033607	PMID:32273475	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0001903	PMID:32273475	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0003593	PMID:32273475	PCS		1/1			C	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0000007	PMID:32273475	PCS					I	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0012136	PMID:32273475	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0001873	PMID:32273475	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:620534	Neutropenia, severe congenital, 10, autosomal recessive		HP:0001875	PMID:32273475	PCS		1/1			P	HPO:probinson[2024-03-12]
OMIM:618915	Deafness, autosomal dominant 77		HP:0000407	PMID:31273342	PCS	HP:0003581	13/13			P	HPO:probinson[2020-08-12];HPO:probinson[2022-07-11]
OMIM:618915	Deafness, autosomal dominant 77		HP:0003581	PMID:31273342	PCS		13/13			C	HPO:probinson[2022-07-11]
OMIM:618915	Deafness, autosomal dominant 77		HP:0000360	PMID:31273342	PCS		0/13			P	HPO:probinson[2022-07-11]
OMIM:618915	Deafness, autosomal dominant 77		HP:0011390	PMID:31273342	PCS		0/13			P	HPO:probinson[2020-08-12];HPO:probinson[2022-07-11]
OMIM:618915	Deafness, autosomal dominant 77		HP:0000006	PMID:31273342	PCS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:616938	Coffin-Siris syndrome 5		HP:0004322	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001250	OMIM:616938	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000280	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0002719	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0009882	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001800	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001305	OMIM:616938	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000219	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000179	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001249	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000154	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001166	OMIM:616938	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000252	OMIM:616938	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001344	PMID:23906836	IEA					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000574	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0009928	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001321	OMIM:616938	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0002079	OMIM:616938	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0011968	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001263	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000294	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0005280	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000508	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0002209	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000527	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001852	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001511	OMIM:616938	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000322	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001631	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000006	PMID:23906836	PCS					I	HPO:probinson[2017-06-25]
OMIM:616938	Coffin-Siris syndrome 5		HP:0001810	OMIM:616938	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616938	Coffin-Siris syndrome 5		HP:0000445	PMID:23906836	PCS					P	HPO:probinson[2017-06-25]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000175	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0002650	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0002162	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000470	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0001629	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000407	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0002949	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000007	OMIM:214300	TAS					I	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000912	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000405	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000466	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000377	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0000204	OMIM:214300	TAS					P	HPO:probinson[2009-02-17]
OMIM:214300	Klippel-Feil syndrome, autosomal recessive		HP:0004602	OMIM:214300	IEA					P	HPO:skoehler[2015-01-27]
OMIM:259200	Blount disease, adolescent		HP:0002970	OMIM:259200	TAS					P	HPO:iea[2009-02-17]
OMIM:259200	Blount disease, adolescent		HP:0002979	OMIM:259200	TAS					P	HPO:nvasilevsky[2019-03-12]
OMIM:259200	Blount disease, adolescent		HP:0000007	OMIM:259200	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:259200	Blount disease, adolescent		HP:0001426	OMIM:259200	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:259200	Blount disease, adolescent		HP:0010886	OMIM:259200	TAS					P	HPO:probinson[2012-09-20]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0005304	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001674	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001684	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001750	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001680	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0005160	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001629	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001719	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0012020	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001669	PMID:17924340	PCS					P	HPO:probinson[2013-01-09]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001636	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0004935	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0001642	OMIM:613854	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0000006	PMID:17924340	PCS					I	HPO:probinson[2013-08-10]
OMIM:613854	Congenital heart defects, multiple types, 6		HP:0032092	OMIM:613854	IEA					P	HPO:skoehler[2019-02-22]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0002135	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0003510	PMID:23684011	PCS		5/5			P	HPO:skoehler[2013-09-10];HPO:probinson[2024-03-08]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0003577	PMID:23684011	PCS		5/5			C	HPO:probinson[2024-03-08]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0001476	PMID:23684011	PCS		1/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-27]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0000540	PMID:23684011	PCS		3/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-27]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0001085	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0001250	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0100253	OMIM:127000	TAS					P	HPO:probinson[2012-07-30]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0000829	PMID:23684011	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-11-27]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0001903	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0011001	OMIM:127000	TAS					P	HPO:probinson[2012-07-30]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0001518	OMIM:127000	TAS					P	HPO:skoehler[2013-09-10]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0000935	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0008285	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0011220	PMID:23684011	PCS		5/5			P	HPO:skoehler[2013-09-10];HPO:probinson[2024-03-08]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0000519	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0002905	OMIM:127000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0000568	PMID:23684011	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0007862	OMIM:127000	TAS					P	HPO:skoehler[2010-06-20]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0002901	PMID:23684011	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-27]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0001620	PMID:23684011	PCS		2/5			P	HPO:skoehler[2013-09-10];HPO:probinson[2022-11-27]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0000256	OMIM:127000	TAS					P	HPO:probinson[2009-02-17]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0000006	PMID:23684011	PCS					I	HPO:skoehler[2013-09-10];HPO:probinson[2022-11-27]
OMIM:127000	Kenny-caffey syndrome, type 2		HP:0001249	PMID:23684011	PCS		0/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:618901	46,XX sex reversal 5		HP:0001684	PMID:29478779	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618901	46,XX sex reversal 5		HP:0001629	PMID:29478779	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618901	46,XX sex reversal 5		HP:0000062	PMID:29478779	PCS		3/3			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618901	46,XX sex reversal 5		HP:0009112	PMID:29478779	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618901	46,XX sex reversal 5		HP:0100779	PMID:29478779	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618901	46,XX sex reversal 5		HP:0030088	PMID:29478779	PCS		3/3			P	HPO:probinson[2020-08-11]
OMIM:618901	46,XX sex reversal 5		HP:0004383	PMID:29478779	PCS		1/3			P	HPO:probinson[2020-08-11]
OMIM:618901	46,XX sex reversal 5		HP:0000006	PMID:29478779	PCS					I	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:607821	Deafness, autosomal recessive 37		HP:0003577	PMID:12687499	PCS		6/6			C	HPO:probinson[2022-09-25]
OMIM:607821	Deafness, autosomal recessive 37		HP:0001751	PMID:12687499	PCS		1/6			P	HPO:probinson[2013-03-04];HPO:probinson[2022-09-25]
OMIM:607821	Deafness, autosomal recessive 37		HP:0000407	PMID:12687499	PCS	HP:0003577	6/6		HP:0012832	P	HPO:probinson[2013-03-04];HPO:probinson[2022-09-25]
OMIM:607821	Deafness, autosomal recessive 37		HP:0000007	PMID:12687499	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-09-25]
OMIM:607821	Deafness, autosomal recessive 37		HP:0007642	PMID:12687499	PCS		1/6			P	HPO:skoehler[2015-09-11];HPO:probinson[2022-09-25]
OMIM:607821	Deafness, autosomal recessive 37		HP:0000510	PMID:12687499	PCS		1/6			P	HPO:skoehler[2015-09-11];HPO:probinson[2022-09-25]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0003236	PMID:28012042	PCS		2/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0003687	PMID:28012042	PCS		2/9			P	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0002650	PMID:28012042	PCS		5/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0030674	PMID:28012042	PCS		3/11			C	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0011968	PMID:28012042	PCS		8/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0001252	PMID:28012042	PCS		11/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0003593	PMID:28012042	PCS		1/11			C	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0012548	PMID:28012042	PCS		3/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0001270	PMID:28012042	PCS		11/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0100297	PMID:28012042	PCS		4/9			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0011463	PMID:28012042	PCS		3/11			C	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0000602	PMID:28012042	PCS		4/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0000007	PMID:28012042	PCS					I	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0000218	PMID:28012042	PCS		11/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0003327	PMID:28012042	PCS		11/11			P	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0000006	PMID:28012042	PCS					I	HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0003623	PMID:28012042	PCS		4/11			C	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620246	Congenital myopathy 18 due to dihydropyridine receptor defect		HP:0003557	PMID:28012042	PCS		8/9			P	HPO:probinson[2023-06-12]
OMIM:310600	Norrie disease		HP:0000594	PMID:17325173	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:310600	Norrie disease		HP:0007759	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0007957	PMID:17325173	PCS		2/2			P	HPO:probinson[2022-05-06]
OMIM:310600	Norrie disease		HP:0000541	PMID:17325173	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:310600	Norrie disease		HP:0001250	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0003593	PMID:17325173	PCS		2/2			C	HPO:probinson[2022-05-06]
OMIM:310600	Norrie disease		HP:0000709	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0008052	PMID:17325173	PCS		1/2			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-05-06]
OMIM:310600	Norrie disease		HP:0000738	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0000518	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0001419	OMIM:310600	IEA					I	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0000407	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0000726	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0000718	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0000618	OMIM:310600	TAS	HP:0003593				P	HPO:probinson[2014-03-23]
OMIM:310600	Norrie disease		HP:0000568	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0000557	PMID:17325173	PCS		1/2			P	HPO:probinson[2022-05-06]
OMIM:310600	Norrie disease		HP:0000648	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0007973	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0007676	OMIM:310600	IEA					P	HPO:iea[2009-02-17]
OMIM:310600	Norrie disease		HP:0000555	PMID:17325173	PCS		1/2			P	HPO:probinson[2022-05-06]
OMIM:137575	Gigantiform cementoma, familial		HP:0000692	OMIM:137575	TAS					P	HPO:probinson[2009-02-17]
OMIM:137575	Gigantiform cementoma, familial		HP:0001571	OMIM:137575	TAS					P	HPO:probinson[2009-02-17]
OMIM:137575	Gigantiform cementoma, familial		HP:0012328	OMIM:137575	TAS					P	HPO:probinson[2013-08-13]
OMIM:137575	Gigantiform cementoma, familial		HP:0000006	OMIM:137575	TAS					I	HPO:probinson[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000486	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0004443	OMIM:123500	PCS					P	HPO:iea[2012-02-24]
OMIM:123500	Crouzon syndrome		HP:0004442	OMIM:123500	PCS					P	HPO:iea[2012-02-24]
OMIM:123500	Crouzon syndrome		HP:0001250	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0004440	PMID:35235708	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0100621	OMIM:123500	TAS					P	HPO:skoehler[2017-07-13]
OMIM:123500	Crouzon syndrome		HP:0000316	PMID:35235708	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0000678	PMID:35235708	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0000238	PMID:35235708	PCS		1/8			P	HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0000218	PMID:35235708	PCS		7/8			P	HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0004439	OMIM:123500	IEA					P	HPO:skoehler[2015-01-19]
OMIM:123500	Crouzon syndrome		HP:0000413	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0001249	PMID:35235708	PCS		0/8			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0004411	PMID:35235708	PCS		8/8			P	HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0000491	OMIM:123500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:123500	Crouzon syndrome		HP:0011800	PMID:35235708	PCS		8/8			P	HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0010535	OMIM:123500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:123500	Crouzon syndrome		HP:0000509	OMIM:123500	TAS					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000327	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000648	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000505	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0003319	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000405	PMID:35235708	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0002007	OMIM:123500	PCS					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000444	PMID:35235708	PCS		8/8			P	HPO:probinson[2024-08-03]
OMIM:123500	Crouzon syndrome		HP:0000520	PMID:35235708	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0000586	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000006	PMID:7987400	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-31]
OMIM:123500	Crouzon syndrome		HP:0000248	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:123500	Crouzon syndrome		HP:0000303	OMIM:123500	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0000110	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0000473	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0012330	OMIM:314300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0000123	OMIM:314300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0008717	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0010562	OMIM:314300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0002619	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0000028	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0000798	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0000324	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:314300	Torticollis, keloids, cryptorchidism, and renal dysplasia		HP:0000995	OMIM:314300	IEA					P	HPO:iea[2009-02-17]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0001012	PMID:26085578;PMID:18458227	PCS		3/3			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0003477	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0003323	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0003202	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0003236	PMID:26085578	PCS		1/2			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0000365	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0001762	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0001284	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0011463	PMID:18458227	PCS		1/1			C	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0002808	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0011462	PMID:26085578	PCS		2/2			C	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0009830	PMID:26085578	PCS		2/2			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0002936	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0009125	PMID:18458227	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0000158	PMID:26085578	PCS		1/2			P	HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0000006	PMID:18458227	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-01]
OMIM:151800	Lipomatosis, multiple symmetric, with or without peripheral neuropathy		HP:0003557	PMID:26085578	PCS		1/1			P	HPO:probinson[2024-03-01]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0004325	PMID:30057030	PCS		10/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0000252	PMID:30057030	PCS		10/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0004322	PMID:30057030	PCS		10/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0030674	PMID:30057030	PCS		10/10			C	HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0025300	PMID:30057030	PCS		0/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0002020	PMID:30057030	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0010998	PMID:30057030	PCS		7/7			P	HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0009141	PMID:30057030	PCS		1/1			P	HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0002719	PMID:30057030	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0000957	PMID:30057030	PCS		8/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0011342	PMID:30057030	PCS		4/10			P	HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0000007	PMID:30057030	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0003758	PMID:30057030	PCS		3/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0001511	PMID:30057030	PCS	HP:0030674	10/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-07]
OMIM:618097	Microcephaly, growth restriction, and increased sister chromatid exchange 2		HP:0001644	PMID:30057030	PCS		4/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-07]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0003477	PMID:32808683	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0007814	PMID:33764426	PCS		1/6			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0002540	PMID:32808683	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001272	PMID:33764426	PCS		2/8			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001250	PMID:33764426	PCS		2/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001252	PMID:33764426	PCS		8/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001251	PMID:33764426	PCS		7/7			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0003593	PMID:33764426	PCS		4/8			C	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0002061	PMID:33764426	PCS		1/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001270	PMID:33764426	PCS		8/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0000639	PMID:33764426	PCS		5/8			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0011463	PMID:33764426	PCS		4/8			C	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0007325	PMID:32808683	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001249	PMID:33764426	PCS		8/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0006855	PMID:33764426;PMID:32808683	PCS		7/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0008936	PMID:33764426	PCS		2/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0002058	PMID:33764426	PCS		4/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0002454	PMID:33764426	PCS		1/8			P	HPO:probinson[2022-08-14]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001344	PMID:33764426	PCS		3/9			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001260	PMID:33764426	PCS		6/6			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0001263	PMID:32808683	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0012678	PMID:33764426	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0007371	PMID:33764426	PCS		1/8			P	HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0000007	PMID:32808683	PCS					I	HPO:probinson[2021-08-21];HPO:probinson[2021-08-21]
OMIM:619389	Spinocerebellar ataxia, autosomal recessive 29		HP:0000543	PMID:32808683	PCS		1/1			P	HPO:probinson[2021-08-21]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0006988	PMID:31334757	PCS		2/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0009914	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000365	PMID:31334757	PCS		3/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000161	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001250	PMID:31334757	PCS		3/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001274	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0002020	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0004383	PMID:31334757	PCS		3/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0100842	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001629	PMID:31334757	PCS		3/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0008551	PMID:31334757	PCS		2/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001643	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001249	PMID:31334757	PCS					P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0006315	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000176	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000175	PMID:31334757	PCS		3/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000252	PMID:31334757	PCS		8/11			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0030048	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0009927	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001263	PMID:31334757	PCS					P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000609	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001419	PMID:31334757	PCS					I	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0009099	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001719	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0002507	PMID:31334757	PCS		2/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0008467	PMID:31334757	PCS		3/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0003316	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000347	PMID:31334757	PCS		3/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0000369	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0008428	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0002247	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:301043	Holoprosencephaly 13, X-linked		HP:0001655	PMID:31334757	PCS		1/12			P	HPO:probinson[2020-09-02]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001254	PMID:33272297	PCS		26/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001297	OMIM:311250	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0003572	OMIM:311250	IEA		30/63			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001250	OMIM:311250	IEA		17/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:6000334	OMIM:311250	TAS					P	HPO:probinson[2024-02-27]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001251	OMIM:311250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0003593	PMID:33272297	PCS		8/68			C	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0002181	OMIM:311250	IEA					P	HPO:iea[2009-02-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0031964	PMID:33272297	PCS		38/52			P	HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0008151	PMID:33272297	PCS		11/54			P	HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001508	OMIM:311250	IEA					P	HPO:iea[2009-02-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0011463	PMID:33272297	PCS		38/68			C	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0000737	PMID:33272297	PCS		17/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001987	OMIM:311250	IEA		54/54			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001249	OMIM:311250	IEA					P	HPO:iea[2009-02-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0002038	OMIM:311250	IEA					P	HPO:iea[2009-02-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0003623	PMID:33272297	PCS		15/68			C	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0031956	PMID:33272297	PCS		28/38			P	HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0003621	PMID:33272297	PCS		4/68			C	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0002013	PMID:33272297	PCS		48/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0002131	OMIM:311250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0003581	PMID:33272297	PCS		3/68			C	HPO:probinson[2022-05-06];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001263	PMID:33272297	PCS		11/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0033139	PMID:33272297	PCS		51/54			P	HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001419	OMIM:311250	IEA					I	HPO:iea[2009-02-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001951	OMIM:311250	IEA					P	HPO:iea[2009-02-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0003217	OMIM:311250	IEA		12/54			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0003218	PMID:33272297	PCS		53/56			P	HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001950	OMIM:311250	IEA					P	HPO:iea[2009-02-17]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0002027	PMID:33272297	PCS		4/69			P	HPO:probinson[2022-05-06]
OMIM:311250	Ornithine transcarbamylase deficiency, hyperammonemia due to		HP:0001259	PMID:33272297	PCS		31/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:227090	Erythroderma, lethal congenital		HP:0007381	OMIM:227090	IEA					P	HPO:iea[2009-02-17]
OMIM:227090	Erythroderma, lethal congenital		HP:0001508	OMIM:227090	IEA					P	HPO:iea[2009-02-17]
OMIM:227090	Erythroderma, lethal congenital		HP:0003073	OMIM:227090	IEA					P	HPO:iea[2009-02-17]
OMIM:227090	Erythroderma, lethal congenital		HP:0000007	OMIM:227090	IEA					I	HPO:iea[2009-02-17]
OMIM:227090	Erythroderma, lethal congenital		HP:0001522	OMIM:227090	IEA					C	HPO:iea[2009-02-17]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000486	PMID:31585109	PCS		3/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0001651	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0002384	PMID:31585109	PCS		1/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0012469	PMID:31585109	PCS		1/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000319	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0011220	PMID:31585109	PCS		4/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0007165	PMID:31585109	PCS		4/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000316	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000912	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0001249	PMID:31585109	PCS		4/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000358	PMID:31585109	PCS		4/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000494	PMID:31585109	PCS		4/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000054	PMID:31585109	PCS		1/5	MALE		P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000490	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0001263	PMID:31585109	IEA		6/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0002194	PMID:31585109	PCS		1/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0032327	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0005180	PMID:31585109	PCS		1/9		HP:0012825	P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000729	PMID:31585109	PCS		2/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0008765	PMID:31585109	PCS		1/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0001335	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000322	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000006	PMID:31585109	PCS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000369	PMID:31585109	PCS		4/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000343	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0002162	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0001274	PMID:31585109	PCS		7/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0010862	PMID:31585109	PCS		2/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0033105	PMID:31585109	PCS		5/9			P	HPO:probinson[2020-10-13]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0002280	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000739	PMID:31585109	PCS		2/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000337	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0006695	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000219	PMID:31585109	PCS		5/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000659	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000218	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000256	PMID:31585109	PCS		4/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0002558	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0008936	PMID:31585109	PCS		3/9			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000391	PMID:31585109	PCS		3/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0001680	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0005280	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0100710	PMID:31585109	PCS		1/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000506	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0100716	PMID:31585109	PCS		1/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000307	PMID:31585109	PCS		2/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000664	PMID:31585109	PCS		1/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0002007	PMID:31585109	PCS		3/9			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0007018	PMID:31585109	PCS		2/8			P	HPO:probinson[2020-08-12]
OMIM:618929	Agenesis of corpus callosum, cardiac, ocular, and genital syndrome		HP:0000028	PMID:31585109	PCS		3/5			P	HPO:probinson[2020-08-12]
OMIM:621170	Monilethrix 3		HP:0100699	PMID:15744029	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621170	Monilethrix 3		HP:0032470	PMID:15744029;PMID:25557232	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621170	Monilethrix 3		HP:0002299	PMID:15744029;PMID:25557232	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621170	Monilethrix 3		HP:0001596	PMID:15744029;PMID:25557232	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621170	Monilethrix 3		HP:0002293	PMID:25557232	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621170	Monilethrix 3		HP:0007502	PMID:25557232	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:621170	Monilethrix 3		HP:0000006	PMID:25557232	PCS					I	ORCID:0000-0002-0736-9199[2025-10-13]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000286	OMIM:616910	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0003577	OMIM:616910	IEA					C	HPO:skoehler[2019-04-18]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0004313	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000252	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000486	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0004432	PMID:26216346	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0001263	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0003196	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0003175	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0001270	PMID:26216346	PCS		2/4			P	HPO:probinson[2024-03-15]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0010442	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0005280	OMIM:616910	IEA					P	HPO:skoehler[2019-04-18]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0012368	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0002719	PMID:26216346	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000316	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000007	PMID:26216346	PCS					I	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000403	PMID:26216346	PCS		4/5			P	HPO:probinson[2024-03-15]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0002846	PMID:26216346	PCS		0/5			P	HPO:skoehler[2019-02-22];HPO:probinson[2024-03-15]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000405	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0001511	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000047	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000028	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0001249	PMID:26216346	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:616910	Immunodeficiency-Centromeric instability-facial anomalies syndrome 3		HP:0000369	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:614861	Deafness, autosomal recessive 98		HP:0003577	PMID:22678063	PCS		3/3			C	HPO:probinson[2023-03-16]
OMIM:614861	Deafness, autosomal recessive 98		HP:0000407	PMID:22678063	PCS	HP:0003577	3/3		HP:0012829	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-16]
OMIM:614861	Deafness, autosomal recessive 98		HP:0000007	PMID:22678063	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2023-03-16]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000486	PMID:30055078	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0002384	PMID:28859103	PCS		1/9			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0002121	PMID:28859103	PCS		1/9			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0003593	PMID:28859103	PCS					C	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0011015	PMID:30055078	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0033725	PMID:28859103	PCS		1/9			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0011463	PMID:30055078	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000718	OMIM:616521;PMID:30055078;PMID:23033978	PCS		10/12			P	HPO:probinson[2022-03-07];HPO:skoehler[2015-12-30];ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000238	PMID:28859103	PCS		1/9			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0001249	PMID:30055078;PMID:23033978	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000154	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0002059	PMID:28859103	PCS		1/9			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000750	PMID:28859103;PMID:30055078;PMID:23033978	PCS		11/11			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-07-15];HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0002353	PMID:30055078	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000431	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0031936	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0001263	PMID:28859103;PMID:30055078;PMID:23033978	PCS		11/11			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-07-15];HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0002591	PMID:28859103;PMID:30055078	PCS		6/10			P	ORCID:0000-0002-0736-9199[2024-07-15];HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0002194	PMID:28859103	PCS		9/9			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0012810	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000729	PMID:28859103	PCS		3/9			P	HPO:probinson[2022-03-07];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000821	PMID:30055078	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0001319	PMID:23033978	PCS	HP:0003623	1/1			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0003118	PMID:30055078	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0007018	PMID:30055078	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000006	PMID:23033978	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0001513	PMID:28859103;PMID:30055078;PMID:23033978	PCS		7/12			P	HPO:probinson[2022-03-07];HPO:skoehler[2015-12-30];HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-07-15]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0001776	PMID:28859103	PCS		1/9			P	HPO:probinson[2022-03-07]
OMIM:616521	Intellectual developmental disorder, autosomal dominant 39		HP:0000742	PMID:28859103	PCS		1/9			P	HPO:probinson[2022-03-07]
OMIM:600343	Parotid salivary glands, polycystic dysgenetic disease of		HP:0011801	OMIM:600343	TAS					P	HPO:probinson[2022-10-02]
OMIM:600343	Parotid salivary glands, polycystic dysgenetic disease of		HP:0000006	OMIM:600343	TAS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-02]
OMIM:615028	Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive		HP:0001030	PMID:23176819	PCS		3/3			P	HPO:skoehler[2013-06-05];HPO:probinson[2023-05-21]
OMIM:615028	Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive		HP:0011463	PMID:23176819	PCS		3/3			C	HPO:probinson[2023-05-21]
OMIM:615028	Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive		HP:0008066	PMID:23176819	PCS		3/3			P	HPO:probinson[2023-05-21]
OMIM:615028	Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive		HP:0025092	PMID:23176819	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-21]
OMIM:615028	Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive		HP:0000007	PMID:23176819	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2023-05-21]
OMIM:615028	Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive		HP:0000962	PMID:23176819	PCS		1/1		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-05-21]
OMIM:602554	Torsion dystonia with onset in infancy		HP:0003593	OMIM:602554	IEA					C	HPO:iea[2009-02-17]
OMIM:602554	Torsion dystonia with onset in infancy		HP:0000006	OMIM:602554	IEA					I	HPO:iea[2009-02-17]
OMIM:602554	Torsion dystonia with onset in infancy		HP:0001304	OMIM:602554	IEA					P	HPO:iea[2009-02-17]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0005116	PMID:21358634	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0003621	PMID:21358634	PCS					C	HPO:probinson[2022-09-04];HPO:probinson[2024-03-29]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0001762	PMID:21358634	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0004970	PMID:21358634	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0000193	PMID:21358634	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0003581	PMID:21358634	PCS					C	HPO:probinson[2022-09-04];HPO:probinson[2024-03-29]
OMIM:132800	Multiple self-healing squamous epithelioma		HP:0003829	PMID:21358634	PCS					I	HPO:probinson[2024-03-29]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0000316	PMID:21358634	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0034720	PMID:21358634	PCS		18/18			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:132800	Multiple self-healing squamous epithelioma, susceptibility to		HP:0000006	PMID:21358634	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-29]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001397	PMID:24488770	PCS		5/20			P	HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0003577	PMID:24488770;PMID:30761183	PCS		24/24			C	HPO:probinson[2023-07-19];HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000365	PMID:24488770	PCS		3/23			P	HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000089	PMID:24488770	PCS		2/23			P	HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000083	PMID:24488770	PCS		6/23			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0004383	PMID:24488770	PCS		1/19			P	HPO:probinson[2023-02-08];HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0011577	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001629	PMID:24488770	PCS		1/19			P	HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0006159	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001643	PMID:24488770	PCS		1/19			P	HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000510	PMID:24488770	PCS		23/23			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0020049	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000135	PMID:24488770	PCS		9/23			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001249	OMIM:615996	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000750	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0031936	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0002079	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001263	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0003241	OMIM:615996	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0100259	PMID:24488770	PCS		19/23			P	HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0006042	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000007	PMID:24488770	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0004409	OMIM:615996	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000548	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001830	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001631	PMID:24488770	PCS		1/19			P	HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000545	PMID:30761183	PCS		1/1			P	HPO:probinson[2023-07-19]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0001513	PMID:24488770;PMID:30761183	PCS		24/24			P	HPO:probinson[2023-07-19];HPO:skoehler[2014-11-26];HPO:probinson[2023-02-08]
OMIM:615996	Bardet-Biedl syndrome 19		HP:0000126	PMID:24488770	PCS		2/23			P	HPO:probinson[2023-02-08]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0001374	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0004324	OMIM:614450	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0002136	OMIM:614450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0000684	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0031418	OMIM:614450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0002750	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0004482	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0012559	PMID:22168587	TAS					P	HPO:probinson[2014-01-04]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0000958	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0001903	OMIM:614450	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0001609	OMIM:614450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0000316	OMIM:614450	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0001539	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0002329	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0000158	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0000851	OMIM:614450	TAS					P	HPO:probinson[2013-03-10]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0002645	OMIM:614450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0002019	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0001510	OMIM:614450	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0000006	OMIM:614450	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614450	Hypothyroidism, congenital, nongoitrous, 6		HP:0002930	OMIM:614450	TAS					P	HPO:probinson[2014-01-04]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000044	PMID:27616479	PCS		3/4			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000286	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000582	OMIM:617159	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000483	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000365	PMID:27616479	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000243	OMIM:617159	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0004322	PMID:27616479	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000062	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000083	PMID:27616479	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001252	PMID:27616479	PCS		4/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0002141	PMID:27479907	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0012745	OMIM:617159	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000280	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0100864	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001629	PMID:27479907	PCS		2/6			P	HP:probinson[2018-05-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001629	PMID:27616479	PCS	HP:0003577	2/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000316	PMID:27616479	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0002119	PMID:27616479	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001643	PMID:27616479	PCS	HP:0003577	2/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000378	PMID:27616479	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000894	PMID:27479907	PCS		1/6			P	HP:probinson[2018-05-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000256	PMID:27616479	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001249	PMID:27616479	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0002677	PMID:27616479	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001545	PMID:27616479	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000076	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000054	PMID:27616479	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000193	PMID:27616479	PCS		1/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001263	PMID:27616479	PCS		5/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001680	PMID:27479907	PCS		1/6			P	HP:probinson[2018-05-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001182	OMIM:617159	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0003180	OMIM:617159	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000508	PMID:27479907	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0002949	PMID:27616479	PCS		2/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001636	PMID:27479907	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0002308	PMID:27616479	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0002645	PMID:27479907	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001631	PMID:27479907	PCS		2/6			P	HP:probinson[2018-05-13]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0001631	PMID:27616479	PCS	HP:0003577	2/5			P	HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000369	PMID:27616479	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000028	PMID:27616479	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:617159	Sifrim-Hitz-Weiss syndrome		HP:0000006	PMID:27616479	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0002224	PMID:17924338	PCS		0/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0003581	PMID:17924338	PCS		3/3			C	HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0010872	PMID:17924338	PCS		1/1			P	HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0011663	PMID:17924338	PCS		3/3			P	HPO:probinson[2013-03-11];HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0004308	PMID:17924338	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0001279	PMID:17924338	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0000982	PMID:17924338	PCS		0/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0006677	PMID:17924338	PCS		1/1			P	HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0000006	PMID:17924338	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-07-03]
OMIM:611528	Arrhythmogenic right ventricular dysplasia 12		HP:0004756	PMID:17924338	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2021-07-03]
OMIM:606054	Propionic acidemia		HP:0001254	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0006846	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001332	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0004322	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001250	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0003353	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0002240	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0000939	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001508	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001903	OMIM:606054	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606054	Propionic acidemia		HP:0001944	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001943	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001987	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0008872	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0002019	OMIM:606054	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606054	Propionic acidemia		HP:0003108	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001942	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0003128	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0008936	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0002059	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0002013	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0410066	PMID:22626821;PMID:19551947	PCS		20/20			P	HPO:NicoleVasilevsky[2018-02-23];HPO:NicoleVasilevsky[2018-03-02]
OMIM:606054	Propionic acidemia		HP:0002154	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001263	OMIM:606054	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0004396	OMIM:606054	TAS					P	HPO:probinson[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0011695	OMIM:606054	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:606054	Propionic acidemia		HP:0002509	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0000007	OMIM:606054	IEA					I	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0000964	OMIM:606054	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606054	Propionic acidemia		HP:0001638	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0002789	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001873	OMIM:606054	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606054	Propionic acidemia		HP:0001733	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001876	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0002104	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001259	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:606054	Propionic acidemia		HP:0001875	OMIM:606054	IEA					P	HPO:iea[2009-02-17]
OMIM:619174	Deafness, autosomal recessive 117		HP:0001751	PMID:33496845	PCS		0/3			P	HPO:probinson[2021-03-27]
OMIM:619174	Deafness, autosomal recessive 117		HP:0000407	PMID:33496845	PCS	HP:0011463	3/3			P	HPO:probinson[2021-03-27]
OMIM:619174	Deafness, autosomal recessive 117		HP:0011463	PMID:33496845	PCS		3/3			C	HPO:probinson[2024-03-16]
OMIM:619174	Deafness, autosomal recessive 117		HP:0000007	PMID:33496845	PCS					I	HPO:probinson[2021-03-27];HPO:probinson[2021-03-27]
OMIM:616247	Long QT syndrome 14		HP:0012819	PMID:27374306	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:616247	Long QT syndrome 14		HP:0001663	PMID:27374306;PMID:23388215	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-06];HPO:probinson[2022-07-09];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:616247	Long QT syndrome 14		HP:0001695	PMID:27374306;PMID:23388215	PCS		4/4			P	HPO:skoehler[2015-03-22];HPO:probinson[2021-07-06];HPO:probinson[2022-07-09];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:616247	Long QT syndrome 14		HP:0003593	PMID:23388215	PCS		2/3			C	HPO:probinson[2021-07-06];HPO:probinson[2022-07-09]
OMIM:616247	Long QT syndrome 14		HP:0005184	PMID:27374306;PMID:23388215	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-06];HPO:probinson[2022-07-09];ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:616247	Long QT syndrome 14		HP:0034305	PMID:23388215	PCS		2/3			P	HPO:probinson[2022-10-07]
OMIM:616247	Long QT syndrome 14		HP:0031677	PMID:27374306;PMID:23388215	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:616247	Long QT syndrome 14		HP:0012266	PMID:23388215	PCS		3/3			P	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06];HPO:probinson[2022-07-09]
OMIM:616247	Long QT syndrome 14		HP:0011463	PMID:27374306	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:616247	Long QT syndrome 14		HP:0001657	OMIM:616247	IEA					P	HPO:skoehler[2015-07-29]
OMIM:616247	Long QT syndrome 14		HP:0000006	PMID:23388215	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-06]
OMIM:616247	Long QT syndrome 14		HP:0003623	PMID:23388215	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-05-05]
OMIM:616247	Long QT syndrome 14		HP:0001699	OMIM:616247	TAS					P	HPO:skoehler[2015-12-30]
OMIM:605549	Cone-Rod dystrophy 8		HP:0007703	OMIM:605549	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605549	Cone-Rod dystrophy 8		HP:0009926	OMIM:605549	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000662	OMIM:605549	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000980	OMIM:605549	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605549	Cone-Rod dystrophy 8		HP:0008043	OMIM:605549	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000608	OMIM:605549	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000618	OMIM:605549	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000613	OMIM:605549	TAS					P	HPO:skoehler[2012-11-21]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000007	OMIM:605549	TAS					I	HPO:skoehler[2012-10-17]
OMIM:605549	Cone-Rod dystrophy 8		HP:0007994	OMIM:605549	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000548	OMIM:605549	IEA					P	HPO:skoehler[2015-01-19]
OMIM:605549	Cone-Rod dystrophy 8		HP:0000587	OMIM:605549	TAS					P	HPO:skoehler[2012-11-21]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000077	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000164	OMIM:615982	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0003577	PMID:15654695	PCS		3/3			C	HPO:probinson[2022-08-08]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000662	PMID:15654695	PCS	HP:0003621	3/3			P	HPO:skoehler[2014-11-26];HP:probinson[2019-04-14]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0001156	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0003241	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0010442	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000107	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000546	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000007	PMID:11381270	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-04-14]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000510	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0001159	PMID:15654695	PCS		2/3			P	HPO:skoehler[2014-11-26];HP:probinson[2019-04-14]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000135	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0000028	PMID:15654695	PCS		2/2	MALE		P	HPO:skoehler[2014-11-26];HP:probinson[2019-04-14]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0001513	OMIM:615982	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615982	Bardet-Biedl syndrome 4		HP:0001249	PMID:15654695	PCS		1/3			P	HPO:skoehler[2014-11-26];HP:probinson[2019-04-14]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001265	OMIM:614322;PMID:24369382	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2012-10-17]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0002069	PMID:24369382	PCS	HP:0003593	6/6			P	HPO:probinson[2022-11-06]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0000252	OMIM:614322	TAS					P	HPO:skoehler[2014-03-24]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0000640	OMIM:614322;PMID:24369382	PCS		16/16			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2012-10-17]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0002353	PMID:24369382	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0003487	PMID:24369382	PCS		2/5			P	HPO:skoehler[2014-03-24];HPO:probinson[2022-11-06];HPO:probinson[2024-03-27]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001272	OMIM:614322	TAS				HP:0012825	P	HPO:skoehler[2014-03-24]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0002066	OMIM:614322;PMID:24369382	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2012-10-17]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001260	OMIM:614322;PMID:24369382	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2012-10-17]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001263	OMIM:614322;PMID:24369382	PCS		16/16			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2012-10-17]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0003593	PMID:24369382	PCS		3/6			C	HPO:probinson[2022-11-06];HPO:probinson[2024-03-27]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001251	PMID:24369382	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0002061	PMID:24369382	PCS		2/6			P	HPO:probinson[2022-11-06]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0002070	OMIM:614322	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0011463	PMID:24369382	PCS		3/6			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0000546	OMIM:614322	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0000007	PMID:24369382	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0000648	OMIM:614322	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001257	PMID:24369382	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001510	OMIM:614322	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0001249	PMID:24369382	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-06]
OMIM:614322	Spinocerebellar ataxia, autosomal recessive 12		HP:0006855	PMID:24369382	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:604131	ALPHA-THALASSEMIA		HP:0011907	OMIM:604131	TAS					P	HPO:probinson[2013-02-17]
OMIM:604131	ALPHA-THALASSEMIA		HP:0004840	OMIM:604131	TAS					P	HPO:probinson[2013-01-09]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0000561	OMIM:602540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0003577	PMID:12072059	IEA		1/1			C	HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0002860	PMID:12072059	PCS	HP:0011462	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0001761	OMIM:602540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0004552	OMIM:602540	TAS					P	HPO:skoehler[2012-11-21]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0011859	OMIM:602540	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0003593	OMIM:602540	TAS					C	HPO:skoehler[2012-10-17]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0031288	PMID:12072059	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0045075	PMID:12072059	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0008064	PMID:12072059	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0000407	PMID:12072059	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0002209	PMID:12072059	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0001019	PMID:12072059	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0000653	PMID:12072059	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0000972	PMID:12072059	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0000982	OMIM:602540	TAS					P	HPO:skoehler[2012-11-21]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0000006	OMIM:602540	TAS					I	HPO:skoehler[2012-10-17]
OMIM:602540	Ichthyosis, hystrix-like, with deafness		HP:0000962	OMIM:602540	TAS					P	HPO:skoehler[2012-11-21]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002069	PMID:33880529	PCS		2/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0003577	PMID:33880529	PCS		5/16			C	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002188	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002384	PMID:33880529	PCS		2/16			P	HPO:probinson[2022-02-26];HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0001272	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002121	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0003593	PMID:33880529	PCS		6/16			C	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0010841	PMID:33880529	PCS		9/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0033725	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0012650	PMID:33880529	PCS		9/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0011463	PMID:33880529	PCS		4/16			C	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0006892	PMID:33880529	PCS		2/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0007366	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002119	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0020049	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0001249	PMID:33880529	PCS					P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0025517	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0003623	PMID:33880529	PCS		1/16			C	HPO:probinson[2022-02-26];HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0025430	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0000252	PMID:33880529	PCS		8/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0006813	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0001385	PMID:33880529	PCS		2/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002133	PMID:33880529	PCS		8/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0025097	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002871	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0001263	PMID:33880529	PCS		13/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0011097	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0007074	PMID:33880529	PCS		2/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0032792	PMID:33880529	PCS		3/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0031165	PMID:33880529	PCS		3/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0002307	PMID:33880529	PCS		1/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0007359	PMID:33880529	PCS		7/16			P	HPO:probinson[2022-02-26]
OMIM:619606	Developmental and epileptic encephalopathy 99		HP:0000006	PMID:33880529	PCS					I	HPO:probinson[2022-02-26];HPO:probinson[2022-02-26]
OMIM:616535	Thyroid cancer, nonmedullary, 5		HP:0040198	OMIM:616535	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616535	Thyroid cancer, nonmedullary, 5		HP:0000006	OMIM:616535	TAS					I	HPO:skoehler[2015-12-30]
OMIM:180730	Rombo syndrome		HP:0007380	OMIM:180730	IEA					P	HPO:iea[2009-02-17]
OMIM:180730	Rombo syndrome		HP:0002671	OMIM:180730	PCS					P	HPO:iea[2009-02-17]
OMIM:180730	Rombo syndrome		HP:0000499	OMIM:180730	PCS					P	HPO:iea[2012-02-21]
OMIM:180730	Rombo syndrome		HP:0000006	OMIM:180730	IEA					I	HPO:iea[2009-02-17]
OMIM:180730	Rombo syndrome		HP:0000534	OMIM:180730	PCS					P	HPO:iea[2009-02-17]
OMIM:268220	Rhabdomyosarcoma 2, alveolar		HP:0006779	OMIM:268220	TAS					P	HPO:iea[2009-02-17]
OMIM:268220	Rhabdomyosarcoma 2, alveolar		HP:0001442	OMIM:268220	TAS					I	HPO:skoehler[2019-04-18]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0003510	PMID:10742114	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0003521	PMID:12746394	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0002751	PMID:12746394;PMID:12833407;PMID:15200511	PCS		14/15			P	HPO:probinson[2022-05-29];HPO:probinson[2022-06-26];HP:probinson[2019-03-01]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0003422	PMID:12746394;PMID:15200511	PCS		12/13			P	HPO:probinson[2022-05-29];HP:probinson[2019-03-01];HP:probinson[2019-03-01]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0003310	OMIM:277300	TAS					P	HPO:probinson[2009-02-17]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0004322	PMID:15200511	PCS		3/3			P	HPO:probinson[2022-05-29]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:6000652	PMID:26167215	PCS					P	HPO:probinson[2024-05-09]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0000470	PMID:12833407;PMID:15200511;PMID:10742114	PCS		14/15			P	HPO:probinson[2022-05-29];HPO:probinson[2022-06-26];HPO:probinson[2009-02-17];HP:probinson[2019-03-01];HPO:probinson[2022-05-29]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0003270	PMID:10742114	PCS					P	HP:probinson[2019-03-01]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0000902	PMID:12833407	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-26]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0002937	PMID:15200511	PCS		2/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0002948	PMID:12833407;PMID:15200511	PCS		4/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-29];HPO:probinson[2022-06-26]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0011461	PMID:12833407	IEA		2/2			C	HPO:probinson[2022-06-26]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0000007	PMID:12746394	PCS					I	HPO:probinson[2009-02-17];HP:probinson[2019-03-01]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0003418	PMID:29765785;PMID:15200511	PCS		3/4			P	HPO:probinson[2022-05-29];HP:probinson[2019-03-01]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0001538	PMID:12833407	PCS		2/2			P	HPO:probinson[2022-06-26]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0003305	OMIM:277300	TAS					P	HPO:probinson[2009-02-17]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0001522	OMIM:277300	TAS					C	HPO:probinson[2009-02-17]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0002205	OMIM:277300	TAS					P	HPO:probinson[2009-02-17]
OMIM:277300	Spondylocostal dysostosis, autosomal recessive 1		HP:0000476	PMID:12833407	PCS		1/2			P	HPO:probinson[2022-06-26]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0000023	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0001382	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0001075	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0001848	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0002816	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0000767	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0000007	OMIM:225320	IEA					I	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0000978	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0000977	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0001659	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0001653	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0001763	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0000963	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0000974	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:225320	Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form		HP:0001634	OMIM:225320	IEA					P	HPO:iea[2009-02-17]
OMIM:600419	Angiokeratoma corporis diffusum with arteriovenous fistulas		HP:0000975	OMIM:600419	TAS					P	HPO:probinson[2012-07-21]
OMIM:600419	Angiokeratoma corporis diffusum with arteriovenous fistulas		HP:0004947	OMIM:600419	TAS					P	HPO:probinson[2012-07-21]
OMIM:600419	Angiokeratoma corporis diffusum with arteriovenous fistulas		HP:0001528	OMIM:600419	TAS					P	HPO:probinson[2012-07-21]
OMIM:600419	Angiokeratoma corporis diffusum with arteriovenous fistulas		HP:0001071	OMIM:600419	IEA					P	HPO:iea[2009-02-17]
OMIM:600419	Angiokeratoma corporis diffusum with arteriovenous fistulas		HP:0000006	OMIM:600419	IEA					I	HPO:iea[2009-02-17]
OMIM:606068	Retinitis pigmentosa 28		HP:0001133	PMID:20705278	PCS					P	HPO:probinson[2013-02-23]
OMIM:606068	Retinitis pigmentosa 28		HP:0007737	PMID:20705278	PCS					P	HPO:probinson[2013-02-23]
OMIM:606068	Retinitis pigmentosa 28		HP:0000662	PMID:20705278	PCS					P	HPO:probinson[2013-02-23]
OMIM:606068	Retinitis pigmentosa 28		HP:0000007	PMID:20705278	PCS					I	HPO:probinson[2013-01-09]
OMIM:606068	Retinitis pigmentosa 28		HP:0000510	PMID:20705278	PCS					P	HPO:probinson[2013-02-23]
OMIM:606068	Retinitis pigmentosa 28		HP:0000543	PMID:20705278	PCS					P	HPO:probinson[2013-02-23]
OMIM:601707	Curry-Jones syndrome		HP:0002025	OMIM:601707	IEA					P	HPO:iea[2009-02-17]
OMIM:601707	Curry-Jones syndrome		HP:0001177	PMID:27236920	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0003577	PMID:27236920	PCS		10/10			C	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0001355	PMID:27236920	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0004389	PMID:27236920	PCS		2/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0001274	PMID:27236920	PCS		7/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0000581	OMIM:601707	IEA					P	HPO:iea[2009-02-17]
OMIM:601707	Curry-Jones syndrome		HP:0011318	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0032612	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0025480	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0011315	PMID:27236920	PCS		4/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0012450	PMID:27236920	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0000612	PMID:27236920	PCS		4/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0009942	PMID:27236920	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0002119	PMID:27236920	PCS		6/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0002436	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0001841	PMID:27236920	PCS		3/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0007206	PMID:27236920	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0001007	PMID:27236920	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0010815	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0025770	PMID:27236920	PCS		8/10			P	HPO:probinson[2024-08-03];HPO:probinson[2024-08-03]
OMIM:601707	Curry-Jones syndrome		HP:0001442	PMID:27236920	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0001263	PMID:27236920	PCS		8/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0100267	PMID:27236920	PCS		2/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0011304	PMID:27236920	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0009890	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0007099	PMID:27236920	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0000646	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0000568	PMID:27236920	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0009779	PMID:27236920	PCS		3/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0002645	PMID:27236920	PCS		1/10			P	HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0002566	PMID:27236920	PCS		4/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0002126	PMID:27236920	PCS		2/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-04]
OMIM:601707	Curry-Jones syndrome		HP:0000324	PMID:27236920	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-04]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000286	PMID:19363806	PCS		14/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0010804	PMID:19363806	PCS		11/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0002023	PMID:19363806	PCS		2/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000486	PMID:19363806	PCS		9/10			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000365	PMID:19363806	PCS		2/10			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000684	PMID:19363806	PCS		2/6			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0004322	PMID:19363806	PCS		6/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000243	PMID:19363806	PCS		12/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0002021	PMID:19363806	PCS		1/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001250	PMID:19363806	PCS		2/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001252	PMID:19363806	PCS		11/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0410030	PMID:19363806	PCS		2/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0100600	PMID:19363806	PCS		2/7	MALE		P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000957	PMID:19363806	PCS		2/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000718	PMID:19363806	PCS		5/9			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000316	PMID:19363806	PCS		14/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000954	PMID:19363806	PCS		6/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001845	PMID:19363806	PCS		8/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0009622	PMID:19363806	PCS		8/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000752	PMID:19363806	PCS		5/9			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001643	PMID:19363806	PCS	HP:0003577	1/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001642	PMID:19363806	PCS		1/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000358	PMID:19363806	PCS		12/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000252	PMID:19363806	PCS		8/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000453	PMID:19363806	PCS		1/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000490	PMID:19363806	PCS		9/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001182	PMID:19363806	PCS		4/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0012385	PMID:19363806	PCS		2/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000568	PMID:19363806	PCS		2/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000048	PMID:19363806	PCS		2/7	MALE		P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0009778	PMID:19363806	PCS		6/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000322	PMID:19363806	PCS		7/12			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000047	PMID:19363806	PCS		3/7	MALE		P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000006	PMID:19363806	PCS					I	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000248	PMID:19363806	PCS		8/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0002323	PMID:19363806	PCS	HP:0003577	1/14			P	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000340	PMID:19363806	PCS		10/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0002089	PMID:19363806	PCS	HP:0003577	2/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000540	PMID:19363806	PCS		2/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001274	PMID:19363806	PCS	HP:0003577	1/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0002084	PMID:19363806	PCS	HP:0003577	1/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0012725	PMID:19363806	PCS		2/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0040079	PMID:19363806	PCS		4/9			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001305	PMID:19363806	PCS	HP:0003577	3/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0009765	PMID:19363806	PCS		8/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000218	PMID:19363806	PCS		11/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000774	PMID:19363806	PCS		8/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000212	PMID:19363806	PCS		2/12			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001545	PMID:19363806	PCS		1/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001762	PMID:19363806	PCS		6/26			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000431	PMID:19363806	PCS		13/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001245	PMID:19363806	PCS		9/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0005487	PMID:19363806	PCS		10/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000194	PMID:19363806	PCS		9/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001518	PMID:19363806	PCS	HP:0003577	10/11			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0001712	PMID:19363806	PCS		1/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000348	PMID:19363806	PCS		11/13			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0006288	PMID:19363806	PCS		1/6			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000347	PMID:19363806	PCS		5/14			P	HPO:probinson[2021-03-13]
OMIM:619148	Chromosome 13q33-q34 deletion syndrome		HP:0000028	PMID:19363806	PCS		2/4	MALE		P	HPO:probinson[2021-03-13]
OMIM:269880	Short syndrome		HP:0000483	PMID:23810378	PCS		5/11			P	HPO:probinson[2023-02-21];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0000684	PMID:23810378	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000485	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0003074	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000518	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0011220	PMID:23810378	PCS		8/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0007485	PMID:23810378	PCS		8/8			P	HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000558	PMID:23810378	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0008499	PMID:23810378	PCS		4/5			P	HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0009466	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000831	PMID:23810378	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0002750	PMID:23810378	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000331	PMID:23810378	PCS		18/18			P	HPO:probinson[2023-02-21];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0003561	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0001382	PMID:23810378	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000490	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0011800	PMID:23810378	PCS		14/16			P	HPO:probinson[2024-03-09];HPO:skoehler[2017-07-13];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0010751	OMIM:269880	IEA					P	HPO:skoehler[2010-06-18]
OMIM:269880	Short syndrome		HP:0100578	OMIM:269880	TAS					P	HPO:skoehler[2015-12-30]
OMIM:269880	Short syndrome		HP:0000407	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000689	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0003758	PMID:23810378	PCS		8/8			P	HPO:probinson[2024-03-09];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0000400	OMIM:269880	IEA		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000565	PMID:23810378	PCS		2/10			P	HPO:probinson[2023-02-21];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0001015	PMID:23810378	PCS		5/7			P	HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000006	PMID:23810378	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000963	PMID:23810378	PCS		5/7			P	HPO:skoehler[2013-08-07];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0000325	PMID:23810378	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000369	PMID:23810378	PCS		18/18			P	HPO:probinson[2023-02-21];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0000023	PMID:23810378	PCS		0/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000540	PMID:23810378	PCS		4/5			P	HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0002715	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000855	PMID:23810378	PCS		7/7			P	HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0009125	OMIM:269880	IEA					P	HPO:skoehler[2015-01-21]
OMIM:269880	Short syndrome		HP:0030084	OMIM:269880	TAS					P	HPO:skoehler[2014-09-21]
OMIM:269880	Short syndrome		HP:0002714	OMIM:269880	TAS					P	HPO:skoehler[2017-07-13]
OMIM:269880	Short syndrome		HP:0000138	PMID:23810378	PCS		3/3			P	HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000138	PMID:23810378	PCS		3/3	FEMALE		P	HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0000750	PMID:23810378	PCS		4/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000431	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000430	PMID:23810378	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0003100	PMID:23810378	PCS		2/6			P	HPO:probinson[2023-02-21];HPO:probinson[2024-03-09]
OMIM:269880	Short syndrome		HP:0010580	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0100678	PMID:23810378	PCS		5/7			P	HPO:skoehler[2013-06-03];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0001518	PMID:23810378	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000506	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000668	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0002007	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0001511	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000501	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:269880	Short syndrome		HP:0000347	PMID:23810378	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0000545	PMID:23810378	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:269880	Short syndrome		HP:0001952	OMIM:269880	IEA					P	HPO:iea[2009-02-17]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0002069	PMID:26048982	PCS		2/3			P	HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0001344	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0002353	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0002133	PMID:26048982	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0001263	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0001252	PMID:26048982	PCS	HP:0003593	3/3			P	HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0003593	PMID:26048982	PCS		6/6			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0001270	PMID:26048982	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0100660	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0000718	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0000712	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0000007	PMID:26048982	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0000733	PMID:26048982	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0000713	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0002307	PMID:26048982	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0001249	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:617171	Dyskinesia, seizures, and intellectual developmental disorder		HP:0004305	PMID:26048982	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-22]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0002465	OMIM:618242	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0000486	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0003200	PMID:20818383	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001288	OMIM:618242	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0003487	OMIM:618242	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0003198	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0002352	OMIM:618242	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0002121	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001260	OMIM:618242	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001263	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001251	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0002490	PMID:20818383	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0002194	PMID:20818383	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0011923	PMID:20818383	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0000639	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0011463	PMID:20818383	PCS		1/1			C	HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001317	OMIM:618242	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0000007	PMID:20818383	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001257	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0002415	PMID:20818383	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-25]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001510	OMIM:618242	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618242	Mitochondrial complex I deficiency, nuclear type 21		HP:0001347	OMIM:618242	IEA					P	HPO:skoehler[2019-02-15]
OMIM:140500	Heart, malformation of		HP:0004383	OMIM:140500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:140500	Heart, malformation of		HP:0001426	OMIM:140500	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:140500	Heart, malformation of		HP:0000006	OMIM:140500	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0003774	OMIM:137950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0100820	OMIM:137950	IEA					P	HPO:skoehler[2015-01-21]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0000112	OMIM:137950	IEA					P	HPO:iea[2009-02-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0000100	OMIM:137950	IEA					P	HPO:iea[2009-02-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0002907	OMIM:137950	TAS					P	HPO:probinson[2009-02-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0000083	OMIM:137950	TAS					P	HPO:skoehler[2012-10-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0000822	OMIM:137950	IEA					P	HPO:iea[2009-02-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0000093	OMIM:137950	IEA					P	HPO:iea[2009-02-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0000006	OMIM:137950	IEA					I	HPO:iea[2009-02-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0003677	OMIM:137950	TAS					C	HPO:skoehler[2012-10-17]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:0001941	OMIM:137950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:137950	Glomerulopathy with fibronectin deposits 1		HP:6000428	OMIM:137950	TAS					P	HPO:probinson[2024-02-27]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0007793	OMIM:608051	TAS					P	HPO:probinson[2012-07-17]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0007641	OMIM:608051	TAS					P	HPO:probinson[2012-07-17]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0007663	OMIM:608051	TAS					P	HPO:probinson[2015-07-21]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0030629	OMIM:608051	TAS					P	HPO:probinson[2015-07-21]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0000603	OMIM:608051	TAS					P	HPO:probinson[2009-02-17]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0007754	OMIM:608051	TAS					P	HPO:probinson[2009-02-17]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0007722	OMIM:608051	TAS					P	HPO:probinson[2015-07-21]
OMIM:608051	Macular dystrophy, retinal, 2		HP:0000006	OMIM:608051	TAS					I	HPO:probinson[2009-02-17]
OMIM:616509	Cataract 44		HP:0000572	PMID:26200341	PCS					P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-24]
OMIM:616509	Cataract 44		HP:0003577	PMID:26200341	PCS		4/4			C	HPO:probinson[2022-11-24]
OMIM:616509	Cataract 44		HP:0000519	PMID:26200341	PCS		4/4		HP:0012828	P	HPO:skoehler[2015-08-16];HPO:probinson[2022-11-24]
OMIM:616509	Cataract 44		HP:0000007	PMID:26200341	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-24]
OMIM:601075	Aplasia cutis congenita, high myopia, and cone-rod dysfunction		HP:0006934	OMIM:601075	IEA					P	HPO:iea[2009-02-17]
OMIM:601075	Aplasia cutis congenita, high myopia, and cone-rod dysfunction		HP:0000007	OMIM:601075	IEA					I	HPO:iea[2009-02-17]
OMIM:601075	Aplasia cutis congenita, high myopia, and cone-rod dysfunction		HP:0011003	OMIM:601075	IEA					P	HPO:iea[2009-02-17]
OMIM:601075	Aplasia cutis congenita, high myopia, and cone-rod dysfunction		HP:0007536	OMIM:601075	IEA					P	HPO:iea[2009-02-17]
OMIM:109100	Autoimmune disease		HP:0002960	OMIM:109100	IEA					P	HPO:iea[2009-02-17]
OMIM:109100	Autoimmune disease		HP:0030057	OMIM:109100	IEA					P	HPO:iea[2009-02-17]
OMIM:109100	Autoimmune disease		HP:0000006	OMIM:109100	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:618524	Myopathy, congenital, with tremor		HP:0002650	PMID:31025394	PCS		5/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0031947	PMID:31025394	PCS		3/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0001371	PMID:31025394	PCS		7/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0000160	PMID:31025394	PCS		1/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0003691	PMID:31025394	PCS		3/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0002174	PMID:31025394	PCS		6/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0002460	PMID:31025394	PCS					P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0005272	PMID:31025394	PCS		1/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0002938	PMID:31025394	PCS		3/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0000218	PMID:31025394	PCS		3/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0003327	PMID:31025394	PCS		6/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0003701	PMID:31025394	PCS					P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0003306	PMID:31025394	PCS		3/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0000006	PMID:31025394	PCS					I	HPO:probinson[2020-07-19];HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0000347	PMID:31025394	PCS		1/7			P	HPO:probinson[2020-07-19]
OMIM:618524	Myopathy, congenital, with tremor		HP:0003458	PMID:31025394	PCS		2/2			P	HPO:probinson[2020-07-19]
OMIM:613471	Reynolds syndrome		HP:0001396	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0030873	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0003155	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0003493	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0025520	OMIM:613471	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613471	Reynolds syndrome		HP:0011838	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0002240	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0100324	OMIM:613471	IEA					P	HPO:skoehler[2015-12-30]
OMIM:613471	Reynolds syndrome		HP:0100869	PMID:20522425	PCS		1/1			P	HPO:skoehler[2012-11-21]
OMIM:613471	Reynolds syndrome		HP:0001888	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0025710	PMID:20522425	PCS		1/1			C	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0002613	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0002910	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0002239	OMIM:613471	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613471	Reynolds syndrome		HP:0000952	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0001744	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0000214	OMIM:613471	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613471	Reynolds syndrome		HP:0003565	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0003761	OMIM:613471	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613471	Reynolds syndrome		HP:0030167	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0030880	PMID:20522425	PCS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:613471	Reynolds syndrome		HP:0002570	OMIM:613471	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613471	Reynolds syndrome		HP:0012219	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0002829	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0002904	OMIM:613471	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613471	Reynolds syndrome		HP:0000989	OMIM:613471	TAS					P	HPO:skoehler[2015-10-05]
OMIM:613471	Reynolds syndrome		HP:0000006	PMID:20522425	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613471	Reynolds syndrome		HP:0025406	PMID:20522425	PCS		1/1			P	HPO:probinson[2023-03-07]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0001771	PMID:23486992	PCS		3/11			P	HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003236	PMID:22577215	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003555	PMID:22577215	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003731	PMID:22577215	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0001288	PMID:23486992	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0002792	PMID:23486992	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003581	PMID:22577215;PMID:23486992	PCS		21/21			C	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003691	PMID:23486992	PCS		6/11			P	HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0009113	PMID:2376753	PCS	HP:0003581				P	HPO:probinson[2013-02-20];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0008981	PMID:23486992	PCS		3/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0009027	PMID:23486992	PCS	HP:0003581				P	HPO:probinson[2013-02-20];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003749	PMID:22577215	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003805	PMID:22577215	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0002878	OMIM:603689	IEA					P	HPO:skoehler[2019-09-07]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003715	PMID:22577215	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003701	PMID:23486992	PCS	HP:0003581				P	HPO:probinson[2013-02-20];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0002359	PMID:23486992	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003547	OMIM:603689	IEA					P	HPO:skoehler[2019-04-18]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0002877	PMID:23486992	PCS	HP:0003581	4/11			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0000006	PMID:22577215	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003677	PMID:22577215	PCS					C	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003722	PMID:23486992	PCS	HP:0003581				P	HPO:probinson[2013-02-20];HPO:probinson[2020-09-15]
OMIM:603689	Myopathy, myofibrillar, 9, with early respiratory failure		HP:0003557	PMID:22577215	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0003621	PMID:16505173	PCS		2/8			C	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0002224	PMID:16505173	PCS		0/8			P	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0003596	PMID:16505173	PCS		3/8			C	HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0003584	PMID:16505173	PCS		1/8			C	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0410173	PMID:16505173	PCS		1/8			P	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0011712	PMID:16505173	PCS		1/8			P	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0034304	PMID:16505173	PCS		3/8			P	HPO:probinson[2022-09-05]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0011663	PMID:16505173	PCS					P	HPO:probinson[2013-03-11];HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0012248	PMID:16505173	PCS		3/8			P	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0011462	PMID:16505173	PCS		2/8			C	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0006682	PMID:16505173	PCS		5/8			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0032232	PMID:16505173	PCS		1/8			P	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0100749	PMID:16505173	PCS		1/8			P	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0004308	PMID:16505173	PCS		8/8			P	HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0001962	PMID:16505173	PCS		3/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0000006	PMID:16505173	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0001645	PMID:16505173	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-10]
OMIM:610193	Arrhythmogenic right ventricular dysplasia, familial, 10		HP:0004756	PMID:16505173	PCS		3/8			P	HPO:probinson[2013-03-11];HPO:probinson[2022-07-10]
OMIM:151380	Leukemia, acute monocytic		HP:0001442	OMIM:151380	IEA					I	HPO:iea[2009-02-17]
OMIM:151380	Leukemia, acute monocytic		HP:0004845	OMIM:151380	IEA					P	HPO:iea[2009-02-17]
OMIM:137763	Glaucoma - sleep apnea		HP:0010535	OMIM:137763	IEA					P	HPO:skoehler[2015-01-27]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0001671	OMIM:274190	TAS					P	HPO:probinson[2017-08-27]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0001574	OMIM:274190	IEA					P	HPO:iea[2009-02-17]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0004322	OMIM:274190	IEA					P	HPO:iea[2009-02-17]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0004430	OMIM:274190	IEA					P	HPO:iea[2009-02-17]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0000458	OMIM:274190	IEA					P	HPO:iea[2009-02-17]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0000007	OMIM:274190	IEA					I	HPO:iea[2009-02-17]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0009777	OMIM:274190	IEA					P	HPO:iea[2009-02-17]
OMIM:274190	Thumb agenesis, short stature, and immunodeficiency		HP:0000823	OMIM:274190	IEA					P	HPO:iea[2009-02-17]
OMIM:614493	Wiskott-Aldrich syndrome 2		HP:0012177	PMID:22231303	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:614493	Wiskott-Aldrich syndrome 2		HP:0002719	PMID:22231303	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:614493	Wiskott-Aldrich syndrome 2		HP:0000964	PMID:22231303	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:614493	Wiskott-Aldrich syndrome 2		HP:0000007	PMID:22231303	PCS					I	HPO:probinson[2013-08-10]
OMIM:614493	Wiskott-Aldrich syndrome 2		HP:0031379	PMID:22231303	PCS		1/1			P	HP:probinson[2018-04-15]
OMIM:614493	Wiskott-Aldrich syndrome 2		HP:0001873	PMID:22231303	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:614493	Wiskott-Aldrich syndrome 2		HP:0005415	PMID:22231303	PCS		1/1			P	HPO:probinson[2013-08-10]
OMIM:102900	Adenosine triphosphate, elevated, of erythrocytes		HP:0001901	OMIM:102900	TAS					P	HPO:probinson[2009-02-17]
OMIM:102900	Adenosine triphosphate, elevated, of erythrocytes		HP:0030271	OMIM:102900	TAS					P	HPO:probinson[2015-01-31]
OMIM:102900	Adenosine triphosphate, elevated, of erythrocytes		HP:0000006	OMIM:102900	TAS					I	HPO:probinson[2009-02-17]
OMIM:246650	Lipase deficiency, combined		HP:0031290	PMID:17994020	PCS		1/1			P	HPO:probinson[2021-07-02]
OMIM:246650	Lipase deficiency, combined		HP:0002155	PMID:17994020	PCS		1/1			P	HPO:probinson[2021-07-02]
OMIM:246650	Lipase deficiency, combined		HP:0011462	PMID:17994020	IEA		1/1			C	HPO:probinson[2021-07-02]
OMIM:246650	Lipase deficiency, combined		HP:0000007	PMID:17994020	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:246650	Lipase deficiency, combined		HP:0009125	PMID:17994020	PCS		1/1			P	HPO:probinson[2021-07-02]
OMIM:246650	Lipase deficiency, combined		HP:0005978	PMID:17994020	PCS		1/1			P	HPO:probinson[2021-07-02]
OMIM:246650	Lipase deficiency, combined		HP:0001733	PMID:17994020	PCS		1/1			P	HPO:probinson[2021-07-02]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0002069	PMID:22022284	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0003676	PMID:22022284	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0001310	PMID:22022284	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0001332	PMID:22022284	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0002123	PMID:22022284	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0001272	PMID:22022284	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0003693	PMID:22022284	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0001251	PMID:22022284	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0003593	PMID:22022284	PCS		1/2			C	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0100543	OMIM:614487	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0007141	PMID:22022284	PCS		1/1			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0007340	PMID:22022284	PCS		2/2			P	HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0011463	PMID:22022284	PCS		1/2			C	HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0000657	PMID:22022284	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0002313	PMID:22022284	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0002015	PMID:22022284	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0002497	PMID:22022284	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0001260	PMID:22022284	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0003383	PMID:22022284	PCS		1/1			P	HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0002075	PMID:22022284	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0012240	OMIM:614487	TAS					P	HPO:probinson[2013-04-01]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0000508	PMID:22022284	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0000007	PMID:22022284	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0001257	PMID:22022284	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614487	Spastic ataxia 5, autosomal recessive		HP:0001336	PMID:22022284	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002982	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0003577	PMID:21407258	PCS		4/5			C	HPO:probinson[2023-01-22];HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0003016	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0004565	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0001552	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0004586	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0004322	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002384	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0001252	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0003593	PMID:21407258	PCS		1/5			C	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000939	PMID:21407258	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000518	PMID:21407258	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0001629	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000938	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000618	PMID:21407258	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0008037	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002757	PMID:21407258	PCS		4/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0007862	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002659	PMID:21407258	PCS		5/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002953	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002756	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0001089	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002751	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000252	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002650	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0001382	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0002808	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000926	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000007	PMID:21407258	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000568	PMID:21407258	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0000667	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0007773	OMIM:259770	IEA					P	HPO:iea[2009-02-17]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0007875	PMID:21407258	PCS		4/5			P	HPO:probinson[2023-01-22]
OMIM:259770	Osteoporosis-pseudoglioma syndrome		HP:0007898	PMID:21407258	PCS		1/5			P	HPO:probinson[2023-01-22]
OMIM:610187	Diaphragmatic hernia 3		HP:0003577	PMID:16103912;PMID:24702427	PCS		7/8			C	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002089	PMID:16103912;PMID:24702427	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0001250	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002066	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0032992	PMID:16103912	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0100247	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0000238	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002878	PMID:16103912;PMID:24702427;PMID:24769157	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0000776	PMID:17568391;PMID:24702427;PMID:24769157	PCS		18/19			P	ORCID:0000-0002-0736-9199[2025-10-05];HPO:probinson[2013-01-09]
OMIM:610187	Diaphragmatic hernia 3		HP:0003621	PMID:24702427	PCS		1/7			C	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002650	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002098	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:6001258	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002092	PMID:24702427	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0005160	PMID:24769157	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0034198	PMID:24769157	PCS		3/3			C	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0009110	PMID:16103912;PMID:24769157	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0000729	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0009112	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0000403	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002107	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0001873	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0000006	PMID:16103912	PCS					I	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0000028	PMID:24702427	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002643	PMID:24702427	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:610187	Diaphragmatic hernia 3		HP:0002566	PMID:24702427	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-05]
OMIM:146830	Immune deficiency, familial variable		HP:0002719	OMIM:146830	TAS					P	HPO:skoehler[2009-02-17]
OMIM:146830	Immune deficiency, familial variable		HP:0000006	OMIM:146830	IEA					I	HPO:iea[2009-02-17]
OMIM:146830	Immune deficiency, familial variable		HP:0002720	OMIM:146830	IEA					P	HPO:iea[2009-02-17]
OMIM:146830	Immune deficiency, familial variable		HP:0002721	OMIM:146830	IEA					P	HPO:iea[2009-02-17]
OMIM:146830	Immune deficiency, familial variable		HP:0004315	OMIM:146830	IEA					P	HPO:iea[2009-02-17]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0034063	PMID:28073829	PCS		0/2			P	HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0003621	PMID:28073829	PCS		1/4			C	HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0003764	PMID:28073829	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0006727	PMID:28073829	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0003593	PMID:28073829	PCS		2/4			C	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0000007	PMID:28073829	PCS					I	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0005518	PMID:28073829	PCS		2/4			P	HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0100651	PMID:28073829	PCS	HP:0003621	4/4			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0001876	PMID:28073829	PCS		3/4			P	HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0025329	PMID:28073829	PCS		0/2			P	HPO:probinson[2022-10-02]
OMIM:620044	Bone marrow failure and diabetes mellitus syndrome		HP:0003623	PMID:28073829	PCS		2/4			C	HPO:probinson[2022-10-02]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0002521	PMID:29100083	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0001264	PMID:29100083	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0001344	PMID:29100083	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0002540	PMID:29100083	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0002133	PMID:29100083	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0011968	PMID:29100083	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0001250	PMID:29100083	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0001263	PMID:29100083	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0005484	PMID:29100083	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0012448	PMID:29100083	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0001290	PMID:29100083	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0000639	PMID:29100083	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0000733	PMID:29100083	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0200134	PMID:29100083	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0000648	PMID:29100083	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0000505	PMID:29100083	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0000006	PMID:29100083	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:617830	Developmental and epileptic encephalopathy 58		HP:0001347	PMID:29100083	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-18]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0001133	OMIM:210370	IEA					P	HPO:iea[2009-02-17]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0000529	PMID:15937078	PCS					P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-20]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0007880	OMIM:210370	IEA					P	HPO:iea[2009-02-17]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0000007	PMID:15937078	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-20]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0000546	OMIM:210370	IEA					P	HPO:iea[2009-02-17]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0007663	PMID:15937078	PCS		9/11			P	HPO:probinson[2022-12-20]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0007675	OMIM:210370	IEA					P	HPO:iea[2009-02-17]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0011003	OMIM:210370	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0030528	OMIM:210370	IEA					P	HPO:skoehler[2018-10-08]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0000531	PMID:15937078	PCS		8/11			P	HPO:probinson[2022-12-20]
OMIM:210370	Bietti crystalline corneoretinal dystrophy		HP:0000533	OMIM:210370	TAS					P	HPO:probinson[2015-07-19]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0002069	PMID:34140661	PCS		1/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0000750	PMID:34140661	PCS		6/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0001344	PMID:34140661	PCS		1/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0002188	PMID:34140661	PCS		1/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0002197	PMID:34140661	PCS		1/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0001272	PMID:34140661	PCS		2/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0001252	PMID:34140661	PCS		5/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0001263	PMID:34140661	PCS		6/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0003593	PMID:34140661	PCS		1/6			C	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0005484	PMID:34140661	PCS		4/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0032794	PMID:34140661	PCS		1/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0032435	PMID:34140661	PCS		1/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0007270	PMID:34140661	PCS		3/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0001903	PMID:34140661	PCS		4/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0002518	PMID:34140661	PCS		2/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0004823	PMID:34140661	PCS		1/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0000006	PMID:34140661	PCS					I	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0003623	PMID:34140661	PCS		5/6			C	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0001875	PMID:34140661	PCS		5/6			P	HPO:probinson[2022-08-13]
OMIM:619835	3-methylglutaconic aciduria, type VIIA, autosomal dominant		HP:0003535	PMID:34140661	PCS		6/6			P	HPO:probinson[2022-08-13]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000286	PMID:1671808	PCS		8/22			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0025386	OMIM:247200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0002389	PMID:1671808	PCS		17/22			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000684	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0002100	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001250	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0003196	PMID:1671808	PCS		26/26			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0010442	OMIM:247200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0012469	OMIM:247200	TAS					P	HPO:skoehler[2013-11-28]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0006191	PMID:1671808	PCS		14/21			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000518	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0007045	PMID:1671808	PCS		13/24			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000954	PMID:1671808	PCS		5/24			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000358	PMID:12621583	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001249	OMIM:247200	TAS		HP:0040280			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000175	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000252	PMID:1671808	PCS		17/25			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0002079	PMID:1671808	PCS		17/23			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0004298	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0011097	OMIM:247200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0012385	OMIM:247200	TAS					P	HPO:skoehler[2013-10-22]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001939	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001339	PMID:1671808	PCS		27/27			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001539	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0004209	PMID:1671808	PCS		10/24			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000125	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000960	PMID:1671808	PCS		14/19			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000006	OMIM:247200	TAS					I	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000369	PMID:1671808	PCS		14/27			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0008947	OMIM:247200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000582	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000023	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000463	OMIM:247200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0002282	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0031882	OMIM:247200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001270	OMIM:247200	TAS		HP:0040280			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001508	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0007020	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0030680	PMID:1671808	PCS		6/27			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000219	OMIM:247200	TAS					P	HPO:skoehler[2013-06-04]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001627	OMIM:247200	TAS					P	HPO:skoehler[2015-12-30]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001302	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001466	OMIM:247200	TAS					I	HPO:skoehler[2012-10-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000215	PMID:1671808	PCS		25/25			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001561	PMID:1671808	PCS		6/20			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000431	PMID:1671808	PCS		24/25			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0009473	PMID:1671808	IEA		6/27			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001558	OMIM:247200	TAS					P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0001511	PMID:1671808;OMIM:247200	PCS		18/32			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0002007	PMID:12621583	PCS		HP:0040281			P	HPO:iea[2010-09-07]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000028	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0000347	PMID:1671808	PCS		26/27			P	HPO:iea[2009-02-17]
OMIM:247200	Miller-Dieker lissencephaly syndrome		HP:0002247	OMIM:247200	TAS					P	HPO:iea[2009-02-17]
OMIM:258320	Omphalocele-Cleft palate syndrome, lethal		HP:0000175	OMIM:258320	TAS					P	HPO:probinson[2009-02-17]
OMIM:258320	Omphalocele-Cleft palate syndrome, lethal		HP:0000193	OMIM:258320	IEA					P	HPO:iea[2009-02-17]
OMIM:258320	Omphalocele-Cleft palate syndrome, lethal		HP:0000007	OMIM:258320	IEA					I	HPO:iea[2009-02-17]
OMIM:258320	Omphalocele-Cleft palate syndrome, lethal		HP:0000238	OMIM:258320	IEA					P	HPO:iea[2009-02-17]
OMIM:258320	Omphalocele-Cleft palate syndrome, lethal		HP:0000813	OMIM:258320	IEA					P	HPO:iea[2009-02-17]
OMIM:258320	Omphalocele-Cleft palate syndrome, lethal		HP:0001539	OMIM:258320	IEA					P	HPO:iea[2009-02-17]
OMIM:258320	Omphalocele-Cleft palate syndrome, lethal		HP:0001522	OMIM:258320	IEA					C	HPO:iea[2009-02-17]
OMIM:615969	Alpha-Fetoprotein deficiency		HP:0000007	PMID:15280901	PCS					I	HPO:skoehler[2015-12-30]
OMIM:615969	Alpha-Fetoprotein deficiency		HP:0045057	PMID:15280901	PCS					P	HPO:skoehler[2015-09-25]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0003301	PMID:1975693	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0003621	PMID:1975693	PCS					C	HPO:probinson[2023-05-18];HPO:probinson[2023-05-18]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0001387	PMID:1975693	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-18]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0004322	OMIM:604864	TAS					P	HPO:skoehler[2009-02-17]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0005086	PMID:1975693	PCS		10/10			P	HPO:skoehler[2013-04-06]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0012313	PMID:1975693	PCS		10/10			P	HPO:probinson[2013-08-10]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0002829	PMID:1975693	PCS		10/10			P	HPO:probinson[2023-05-18]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0011462	PMID:1975693	PCS					C	HPO:probinson[2023-05-18]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0000926	PMID:1975693	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0030041	OMIM:604864	TAS					P	HPO:skoehler[2014-10-10]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0008843	PMID:1975693	PCS		10/10			P	HPO:skoehler[2009-02-17]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0000006	PMID:1975693	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-18]
OMIM:604864	Osteoarthritis with mild chondrodysplasia		HP:0004568	PMID:1975693	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002960	PMID:25627830	PCS		17/136			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002301	OMIM:243700	IEA					P	HPO:iea[2009-02-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0003212	PMID:19776401	PCS		10/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002860	PMID:19776401	PCS		3/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0030991	PMID:25627830	PCS		7/136			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0003593	PMID:19776401	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0410151	PMID:19776401	PCS		2/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0003193	PMID:25627830	PCS		22/97			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0031292	PMID:25627830	PCS		70/84			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0032185	PMID:19776401	PCS		4/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0032163	PMID:25627830	PCS		40/109			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0001508	PMID:25627830	PCS		67/136			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0031691	PMID:25627830	PCS		18/136			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002718	PMID:19776401	PCS		11/11			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0100845	PMID:25627830	PCS		16/97			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0100806	PMID:25627830	PCS		23/79			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0006532	PMID:19776401	PCS		8/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0025419	PMID:25627830	PCS		4/134			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0040218	PMID:19776401	PCS		6/10			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002138	OMIM:243700	IEA					P	HPO:iea[2009-02-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002754	PMID:25627830	PCS		8/79			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002850	PMID:19776401	PCS		11/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0005425	OMIM:243700	TAS					P	HPO:probinson[2009-02-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0410323	PMID:25627830	PCS		9/97			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0001880	PMID:19776401	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0001047	PMID:19776401	PCS		11/11			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002099	PMID:19776401;PMID:25627830	PCS		58/108			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-25];HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002110	PMID:19776401;PMID:25627830	PCS		57/135			P	HPO:probinson[2022-03-25];HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0011108	PMID:19776401	PCS		8/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0500093	PMID:19776401;PMID:25627830	PCS		91/108			P	HPO:probinson[2022-03-25];HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0000007	PMID:19776401	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0000964	PMID:19776401;PMID:25627830	PCS		144/146		HP:0012828	P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-25];HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0000403	PMID:19776401	PCS		10/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0004429	PMID:19776401	PCS		11/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002205	PMID:25627830	PCS		124/136			P	HPO:probinson[2024-01-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0005318	OMIM:243700	IEA					P	HPO:iea[2009-02-17]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0001510	PMID:19776401	PCS		2/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0003237	PMID:19776401	PCS		6/11			P	HPO:probinson[2022-03-25]
OMIM:243700	Hyper-IgE syndrome 2, autosomal recessive, with recurrent infections		HP:0002841	OMIM:243700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000252	PMID:33736665	PCS		6/19			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0003577	PMID:33736665	PCS					C	HPO:probinson[2022-08-28]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000750	PMID:33736665	PCS		21/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0001344	PMID:33736665	PCS		5/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000486	PMID:33736665	PCS		3/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0002376	PMID:33736665	PCS		3/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0004322	PMID:33736665	PCS		8/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0031936	PMID:33736665	PCS		14/20			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0001250	PMID:33736665	PCS		3/20			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0001263	PMID:33736665	PCS		21/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0001252	PMID:33736665	PCS		10/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0003593	PMID:33736665	PCS					C	HPO:probinson[2022-08-28]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000709	PMID:33736665	PCS		1/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000639	PMID:33736665	PCS		1/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000407	PMID:33736665	PCS		12/21			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0002858	PMID:33736665	PCS		2/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000007	PMID:33736665	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0025336	PMID:33736665	PCS		4/12			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0001763	PMID:33736665	PCS		3/20			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000589	PMID:33736665	PCS		1/21			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0000358	PMID:33736665	PCS		7/20			P	HPO:probinson[2022-08-12]
OMIM:618295	Intellectual developmental disorder, autosomal recessive 67		HP:0003623	PMID:33736665	PCS					C	HPO:probinson[2022-08-28]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0003774	PMID:23862974	PCS		3/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-21]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0000076	PMID:23862974	PCS		1/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-21]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0003577	PMID:23862974	PCS					C	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-21]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0000122	PMID:23862974	PCS		1/12			P	HPO:probinson[2023-05-21]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0000089	PMID:23862974	PCS		6/12			P	HPO:probinson[2023-05-21]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0000074	PMID:23862974	PCS		3/12			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-21]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0003829	PMID:23862974	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-21]
OMIM:610805	Congenital anomalies of kidney and urinary tract, susceptibility to		HP:0000006	PMID:23862974	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-21]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0003752	PMID:18835861	PCS		1/1			P	HPO:probinson[2012-04-11];HPO:probinson[2022-08-18]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0002486	PMID:18835861	PCS		0/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-18]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0003198	OMIM:170400	TAS		HP:0040283			P	HPO:skoehler[2012-11-21]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0001252	PMID:18835861	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0003829	OMIM:170400	TAS			FEMALE		I	HPO:skoehler[2012-11-21]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0003593	PMID:18835861	PCS		1/1			C	HPO:probinson[2022-08-18]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0002900	PMID:18835861	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-08-18]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0001324	OMIM:170400	TAS					P	HPO:probinson[2012-04-11]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0003768	PMID:18835861	PCS		1/1			P	HPO:probinson[2022-08-18]
OMIM:170400	Hypokalemic periodic paralysis, type 1		HP:0000006	PMID:8004673	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2022-08-18]
OMIM:203330	Pseudohypoparathyroidism, type II		HP:0003165	OMIM:203330	IEA					P	HPO:iea[2009-02-17]
OMIM:203330	Pseudohypoparathyroidism, type II		HP:0002905	OMIM:203330	IEA					P	HPO:iea[2009-02-17]
OMIM:203330	Pseudohypoparathyroidism, type II		HP:0002901	OMIM:203330	IEA					P	HPO:iea[2009-02-17]
OMIM:203330	Pseudohypoparathyroidism, type II		HP:0003745	OMIM:203330	IEA					I	HPO:iea[2009-02-17]
OMIM:203330	Pseudohypoparathyroidism, type II		HP:0000852	OMIM:203330	IEA					P	HPO:iea[2009-02-17]
OMIM:139000	Granulosis rubra nasi		HP:0011463	OMIM:139000	TAS					C	HPO:probinson[2012-07-17]
OMIM:139000	Granulosis rubra nasi		HP:0000975	OMIM:139000	TAS					P	HPO:probinson[2009-02-17]
OMIM:139000	Granulosis rubra nasi		HP:0000006	OMIM:139000	TAS					I	HPO:probinson[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0001770	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000365	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000486	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0004322	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0004443	OMIM:101400	IEA					P	HPO:iea[2012-02-24]
OMIM:101400	Saethre-Chotzen syndrome		HP:0004440	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0003828	OMIM:101400	IEA					M	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000316	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000557	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0001249	OMIM:101400	IEA		HP:0040283			P	HPO:skoehler[2012-10-09]
OMIM:101400	Saethre-Chotzen syndrome		HP:0002974	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000175	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0003002	OMIM:101400	TAS					P	HPO:skoehler[2013-01-22]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000294	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0011323	OMIM:101400	IEA					P	HPO:iea[2012-02-24]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000327	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0004209	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000444	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0009899	OMIM:101400	TAS					P	HPO:probinson[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000006	OMIM:101400	IEA					I	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000248	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000369	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000324	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000263	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000189	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0001156	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000460	OMIM:101400	TAS					P	HPO:probinson[2012-05-01]
OMIM:101400	Saethre-Chotzen syndrome		HP:0010104	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0012368	OMIM:101400	TAS					P	HPO:skoehler[2013-10-22]
OMIM:101400	Saethre-Chotzen syndrome		HP:0008551	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0001822	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0030680	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0001627	OMIM:101400	TAS					P	HPO:skoehler[2015-12-30]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000614	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0002678	OMIM:101400	TAS					P	HPO:skoehler[2015-01-21]
OMIM:101400	Saethre-Chotzen syndrome		HP:0009968	OMIM:101400	TAS					P	HPO:probinson[2012-06-04]
OMIM:101400	Saethre-Chotzen syndrome		HP:0002697	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0003189	OMIM:101400	TAS					P	HPO:probinson[2012-05-01]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000270	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000272	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000508	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0009951	OMIM:101400	TAS					P	HPO:probinson[2012-06-04]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000348	OMIM:101400	TAS					P	HPO:probinson[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0001159	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0001357	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0000586	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0002644	OMIM:101400	IEA					P	HPO:iea[2009-02-17]
OMIM:101400	Saethre-Chotzen syndrome		HP:0004425	OMIM:101400	IEA					P	HPO:skoehler[2012-10-09]
OMIM:610024	Retinal cone dystrophy 3A		HP:0003621	OMIM:610024	TAS					C	HPO:probinson[2022-09-28];HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0000662	PMID:22901948	PCS		0/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0008020	PMID:22901948	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-25]
OMIM:610024	Retinal cone dystrophy 3A		HP:0000639	PMID:22901948	PCS		2/3			P	HPO:skoehler[2012-12-03];HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0030473	PMID:22901948	PCS		3/3			P	HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0000613	PMID:22901948	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0007663	PMID:22901948	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0007641	PMID:22901948	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0000007	PMID:22901948	PCS					I	HPO:skoehler[2012-12-03];HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0011003	PMID:22901948	PCS		3/3			P	HPO:probinson[2022-09-28]
OMIM:610024	Retinal cone dystrophy 3A		HP:0000006	PMID:22901948	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28];HPO:probinson[2023-03-25]
OMIM:617993	Tumoral calcinosis, hyperphosphatemic, familial, 2		HP:0007618	PMID:16151858	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:617993	Tumoral calcinosis, hyperphosphatemic, familial, 2		HP:0012408	PMID:16151858	PCS		1/1			P	HPO:probinson[2020-08-13]
OMIM:617993	Tumoral calcinosis, hyperphosphatemic, familial, 2		HP:0000007	PMID:16151858	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:617993	Tumoral calcinosis, hyperphosphatemic, familial, 2		HP:0002150	PMID:16151858	PCS		1/1			P	HPO:probinson[2020-08-13]
OMIM:617993	Tumoral calcinosis, hyperphosphatemic, familial, 2		HP:0002986	PMID:16151858	IEA		1/1			P	HPO:probinson[2020-08-13]
OMIM:185700	Symphalangism, distal		HP:0001363	OMIM:185700	IEA					P	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0001792	OMIM:185700	IEA					P	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0001156	OMIM:185700	IEA					P	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0001859	OMIM:185700	IEA					P	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0003828	OMIM:185700	IEA					M	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0001049	OMIM:185700	IEA					P	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0000006	OMIM:185700	IEA					I	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0001204	OMIM:185700	IEA					P	HPO:iea[2009-02-17]
OMIM:185700	Symphalangism, distal		HP:0001798	OMIM:185700	IEA					P	HPO:iea[2009-02-17]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0002002	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0004322	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0001252	PMID:25915598	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0003593	PMID:25915598	PCS		2/2			C	HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0001290	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000280	PMID:25915598	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0012471	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000998	PMID:25915598	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000158	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000212	PMID:25915598	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0001249	PMID:25915598	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0001007	PMID:25915598	PCS		1/2			P	HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000456	PMID:25915598	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000574	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000430	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0005322	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0001263	PMID:25915598	PCS		2/2			P	HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000470	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0002808	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000407	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000349	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000527	PMID:25915598	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000664	PMID:25915598	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0000006	PMID:25915598	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-22]
OMIM:616455	Zimmermann-Laband syndrome 2		HP:0001798	PMID:25915598	PCS		2/2			P	HPO:probinson[2022-04-22]
DECIPHER:20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0000750	DECIPHER:20	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0001252	DECIPHER:20	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0000717	DECIPHER:20	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0000752	DECIPHER:20	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0001249	DECIPHER:20	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614524	Fibrochondrogenesis 2		HP:0003026	PMID:22246659	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0003016	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0003577	PMID:22246659	PCS		2/2			C	HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000463	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0005257	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0001591	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0003196	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0003175	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000272	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0003021	PMID:22246659	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0003173	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0011800	PMID:22246659	PCS		2/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000946	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000926	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000007	PMID:22246659	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000887	PMID:22246659	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0001538	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0002007	PMID:22246659	PCS		2/2			P	HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000773	PMID:22246659	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000006	PMID:22246659	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:614524	Fibrochondrogenesis 2		HP:0000347	PMID:22246659	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-24]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0002069	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0005469	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0010848	PMID:29322246	PCS					P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000494	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000750	PMID:29322246;PMID:31110234	PCS		2/3			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000321	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000574	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000293	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0001263	PMID:29322246;PMID:31110234	PCS		3/3			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0032794	PMID:29322246;PMID:31110234	PCS	HP:0011463	3/3			P	HPO:probinson[2020-11-28];HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0002392	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0001182	PMID:29322246;PMID:31110234	PCS		1/3		HP:0012825	P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0031535	PMID:31110234	PCS		1/1			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0011150	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000729	PMID:29322246	PCS		2/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000739	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000179	PMID:29322246	PCS		1/2			P	HPO:probinson[2020-11-28]
OMIM:619000	Intellectual developmental disorder with seizures and language delay		HP:0000006	PMID:29322246	PCS					I	HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:148000	Kaposi sarcoma, susceptibility to		HP:0001034	OMIM:148000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148000	Kaposi sarcoma, susceptibility to		HP:0002664	OMIM:148000	IEA					P	HPO:iea[2009-02-17]
OMIM:148000	Kaposi sarcoma, susceptibility to		HP:0000969	OMIM:148000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148000	Kaposi sarcoma, susceptibility to		HP:0100726	OMIM:148000	TAS					P	HPO:probinson[2020-01-31]
OMIM:148000	Kaposi sarcoma, susceptibility to		HP:0000006	OMIM:148000	IEA					I	HPO:iea[2009-02-17]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0002069	PMID:15781812;PMID:16021330	PCS		19/22			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0002344	PMID:15781812;PMID:16021330	PCS		18/22			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0003621	PMID:15781812;PMID:16021330	PCS		21/22			C	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0001288	PMID:15781812	PCS		8/14			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0002384	PMID:15781812;PMID:16021330	PCS		1/22			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0010819	PMID:15781812;PMID:16021330	PCS		2/22			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0032794	PMID:15781812;PMID:16021330	PCS		21/22			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0011147	PMID:15781812;PMID:16021330	PCS		6/22			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0100318	PMID:16021330	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0000726	PMID:15781812	PCS		9/17			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0032792	PMID:15781812;PMID:16021330	PCS		0/22			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0011462	PMID:15781812	PCS		1/17			C	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0000007	PMID:15781812	PCS					I	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620681	Myoclonic epilepsy of Lafora 2		HP:0001336	PMID:15781812	PCS		17/17			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0002751	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0003577	PMID:11443545	PCS		1/1			C	HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000252	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000054	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000992	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000365	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000046	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0100490	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000490	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0001263	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0008070	PMID:11443545	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000518	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0003819	PMID:11443545	PCS		2/2			C	HPO:probinson[2022-04-05];HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0001838	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0001518	PMID:11443545	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000519	PMID:11443545	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000448	PMID:11443545	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000007	PMID:11443545	PCS					I	HPO:probinson[2013-04-01]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000568	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000444	PMID:11443545	PCS		2/2			P	HPO:probinson[2023-01-23];HPO:skoehler[2019-04-18];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0001511	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-01-09];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0001510	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:610756	Cerebrooculofacioskeletal syndrome 2		HP:0000347	PMID:11443545	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-04-05]
OMIM:617039	Patent ductus arteriosus 3		HP:0001643	PMID:27181681	PCS	HP:0003577				P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617039	Patent ductus arteriosus 3		HP:0000006	OMIM:617039	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0003235	PMID:20301697;PMID:26667307	PCS		13/13			P	HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001132	PMID:9775245	PCS		13/19			P	HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001297	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001376	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001250	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001010	OMIM:236200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0001251	PMID:26667307	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:6000357	PMID:5647845	PCS					P	HPO:probinson[2024-02-27]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000716	OMIM:236200	TAS					P	HPO:skoehler[2015-12-30]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0011463	PMID:11596648	PCS		4/23			C	HPO:probinson[2022-03-25]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0012075	OMIM:236200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000678	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001249	PMID:20301697;PMID:8755636;PMID:26667307	PCS		14/14			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0003623	PMID:11596648	PCS		19/23			C	HPO:probinson[2022-03-25]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002751	PMID:26667307	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000098	OMIM:236200	TAS				HP:0012825	P	HPO:probinson[2012-03-16]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002156	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0001260	PMID:26667307	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001263	PMID:20301697	IEA					P	HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0031284	PMID:26667307	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000965	OMIM:236200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001658	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000767	PMID:20301697	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000007	PMID:20301697	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000768	PMID:26667307	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001733	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001397	OMIM:236200	TAS					P	HPO:probinson[2012-03-16]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0000541	PMID:26667307	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0004586	OMIM:236200	TAS					P	HPO:probinson[2012-03-16]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000023	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002160	PMID:20301697;PMID:8755636;PMID:26667307	PCS		14/14			P	HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0040160	OMIM:236200	TAS					P	HPO:skoehler[2015-06-22]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0012444	PMID:26667307	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000939	PMID:8755636	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001907	PMID:20301697	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001508	OMIM:236200	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0002317	PMID:26667307	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000218	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0000577	PMID:26667307	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001166	PMID:8755636;PMID:26667307	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2024-06-10];ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria, B6-responsive and nonresponsive types		HP:0003621	PMID:8755636;PMID:26667307	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002650	PMID:20301697	PCS					P	HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002299	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001083	PMID:8755636;PMID:26667307;PMID:9775245;PMID:11641642	PCS		18/37			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02];HP:probinson[2019-03-02];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000708	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001519	PMID:20301697;PMID:8755636	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-06-10];HPO:skoehler[2012-10-17];HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0032352	OMIM:236200	IEA					P	HPO:skoehler[2019-04-18]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000505	PMID:9775245	PCS		4/19			P	HP:probinson[2019-03-02]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000501	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001634	OMIM:236200	IEA					P	HPO:iea[2009-02-17]
OMIM:236200	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000545	PMID:26667307;PMID:9775245	PCS		11/22			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-06-10]
OMIM:228980	Fleck retina, familial benign		HP:0012045	PMID:22137173	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-19]
OMIM:228980	Fleck retina, familial benign		HP:0000662	PMID:22137173	PCS		0/7			P	HPO:skoehler[2013-05-30];HPO:probinson[2023-03-19]
OMIM:228980	Fleck retina, familial benign		HP:0000007	PMID:22137173	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-03-19]
OMIM:228980	Fleck retina, familial benign		HP:0000505	PMID:22137173	PCS		0/7			P	HPO:skoehler[2015-03-28];HPO:probinson[2023-03-19]
DECIPHER:34	Potocki-Shaffer syndrome		HP:0002762	DECIPHER:34	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:34	Potocki-Shaffer syndrome		HP:0002697	DECIPHER:34	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:34	Potocki-Shaffer syndrome		HP:0000270	DECIPHER:34	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:34	Potocki-Shaffer syndrome		HP:0010461	DECIPHER:34	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:34	Potocki-Shaffer syndrome		HP:0001249	DECIPHER:34	IEA					P	HPO:skoehler[2013-05-29]
OMIM:614256	Intellectual developmental disorder, autosomal dominant 10		HP:0001250	PMID:21376300	PCS		0/1			P	HPO:probinson[2022-05-30]
OMIM:614256	Intellectual developmental disorder, autosomal dominant 10		HP:0011463	PMID:21376300	PCS		1/1			C	HPO:probinson[2022-05-30]
OMIM:614256	Intellectual developmental disorder, autosomal dominant 10		HP:0410263	PMID:21376300	PCS		0/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-30]
OMIM:614256	Intellectual developmental disorder, autosomal dominant 10		HP:0000006	PMID:21376300	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-05-30]
OMIM:600223	Spinocerebellar ataxia 4		HP:0001265	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0003487	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0001272	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0001260	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0001284	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0007772	OMIM:600223	IEA					P	HPO:skoehler[2010-06-18]
OMIM:600223	Spinocerebellar ataxia 4		HP:0002073	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0002936	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0002406	OMIM:600223	IEA					P	HPO:iea[2009-02-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0000763	OMIM:600223	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600223	Spinocerebellar ataxia 4		HP:0000006	OMIM:600223	IEA					I	HPO:iea[2009-02-17]
OMIM:232700	Glycogen storage disease VI		HP:0002155	PMID:25266922	PCS					P	HP:probinson[2019-04-13];HP:probinson[2019-04-13]
OMIM:232700	Glycogen storage disease VI		HP:0001531	PMID:25266922	PCS					P	HP:probinson[2019-04-13]
OMIM:232700	Glycogen storage disease VI		HP:0003124	PMID:25266922	PCS					P	HP:probinson[2019-04-13]
OMIM:232700	Glycogen storage disease VI		HP:0003077	OMIM:232700	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:232700	Glycogen storage disease VI		HP:0002240	PMID:25266922	PCS	HP:0003593	4/4			P	HPO:iea[2009-02-17];HP:probinson[2019-04-13]
OMIM:232700	Glycogen storage disease VI		HP:0000007	PMID:25266922	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-13]
OMIM:232700	Glycogen storage disease VI		HP:0001943	PMID:25266922	PCS					P	HPO:skoehler[2012-10-17];HP:probinson[2019-04-13]
OMIM:232700	Glycogen storage disease VI		HP:0008897	OMIM:232700	IEA					P	HPO:iea[2009-02-17]
OMIM:232700	Glycogen storage disease VI		HP:6000979	OMIM:232700	TAS					P	HPO:probinson[2024-08-04]
OMIM:232700	Glycogen storage disease VI		HP:0002910	PMID:25266922	PCS		4/4			P	HP:probinson[2019-04-13]
OMIM:232700	Glycogen storage disease VI		HP:0006568	PMID:25266922	PCS		3/3			P	HPO:iea[2009-02-17];HP:probinson[2019-04-13]
OMIM:265880	PYKNOACHONDROGENESIS		HP:0011001	OMIM:265880	IEA				HP:0012828	P	HPO:iea[2009-02-17]
OMIM:265880	PYKNOACHONDROGENESIS		HP:0003826	OMIM:265880	TAS					C	HPO:skoehler[2009-02-17]
OMIM:265880	PYKNOACHONDROGENESIS		HP:0000007	OMIM:265880	IEA					I	HPO:iea[2009-02-17]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0000252	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0001410	OMIM:615160	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0003542	PMID:23281071	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0002033	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0002572	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0002151	PMID:23281071	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0001263	PMID:23281071	PCS		2/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0033325	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0033504	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0001518	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0033177	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0000007	PMID:23281071	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0001987	PMID:23281071	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0001943	PMID:23281071	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0002876	PMID:23281071	PCS		2/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0002910	OMIM:615160	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0001631	PMID:23281071	PCS		1/3			P	HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0001942	PMID:23281071	PCS		3/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2021-07-08]
OMIM:615160	Mitochondrial complex III deficiency, nuclear type 5		HP:0003348	PMID:23281071	PCS		2/3			P	HPO:probinson[2021-07-08]
OMIM:605373	Paragangliomas 3		HP:0003334	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0006824	OMIM:605373	TAS					P	HPO:probinson[2016-07-19]
OMIM:605373	Paragangliomas 3		HP:0006748	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0006737	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0002331	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0002640	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0008629	OMIM:605373	TAS					P	HPO:probinson[2016-07-22]
OMIM:605373	Paragangliomas 3		HP:0003001	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0003581	PMID:11062460	PCS		5/5			C	HPO:skoehler[2018-03-07];HPO:probinson[2023-02-10]
OMIM:605373	Paragangliomas 3		HP:0001609	OMIM:605373	TAS					P	HPO:probinson[2016-07-25]
OMIM:605373	Paragangliomas 3		HP:0000975	OMIM:605373	TAS					P	HPO:probinson[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0030074	OMIM:605373	TAS					P	HPO:skoehler[2015-01-20]
OMIM:605373	Paragangliomas 3		HP:0001649	OMIM:605373	TAS					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0001605	OMIM:605373	TAS					P	HPO:probinson[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0001962	OMIM:605373	TAS					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0000740	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0001686	OMIM:605373	IEA					P	HPO:iea[2018-03-07]
OMIM:605373	Paragangliomas 3		HP:0002668	PMID:11062460	PCS		5/5			P	HPO:probinson[2023-02-10]
OMIM:605373	Paragangliomas 3		HP:0000006	PMID:11062460	PCS					I	HPO:iea[2018-03-07];HPO:probinson[2023-02-10]
OMIM:609549	Nanophthalmos 2		HP:0000541	PMID:15976030	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:609549	Nanophthalmos 2		HP:0001120	PMID:15976030	PCS		0/5			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:609549	Nanophthalmos 2		HP:0008499	PMID:15976030	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:609549	Nanophthalmos 2		HP:0000007	PMID:15976030	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2025-10-21]
OMIM:609549	Nanophthalmos 2		HP:0000568	PMID:15976030	PCS		5/5			P	HPO:probinson[2013-03-31];HPO:probinson[2025-10-21]
OMIM:609549	Nanophthalmos 2		HP:0007663	PMID:15976030	PCS		5/5			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:609549	Nanophthalmos 2		HP:0012109	PMID:15976030	PCS		1/5			P	ORCID:0000-0002-0736-9199[2025-10-21]
OMIM:616469	Retinitis pigmentosa 72		HP:0001133	PMID:25882705	PCS		3/3			P	HPO:skoehler[2015-08-05];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0007737	PMID:25882705	PCS		3/3			P	HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0000662	PMID:25882705	PCS		3/3			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0003596	PMID:25882705	PCS		1/3			C	HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0011003	PMID:25882705	PCS		1/3			P	HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0500087	PMID:25882705	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0011462	PMID:25882705	PCS		2/3			C	HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0000613	PMID:25882705	PCS		2/3			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0007663	PMID:25882705	PCS		3/3			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0000007	PMID:25882705	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0000543	PMID:25882705	PCS		3/3			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0007787	PMID:25882705	PCS		3/3			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0000510	PMID:25882705	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-12]
OMIM:616469	Retinitis pigmentosa 72		HP:0007843	PMID:25882705	PCS		3/3			P	HPO:probinson[2022-09-12]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0001382	PMID:38433265	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0005113	PMID:38433265	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0004970	PMID:38433265	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:6000342	PMID:38433265	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0001075	PMID:38433265	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0003010	PMID:38433265	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0011898	PMID:38433265	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0005293	PMID:38433265	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0011873	PMID:38433265	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0100550	PMID:38433265	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0030976	PMID:38433265	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0025509	PMID:38433265	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0012095	PMID:38433265	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0008330	PMID:38433265	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0032199	PMID:38433265	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0000978	PMID:38433265	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0001638	PMID:38433265	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0000974	PMID:38433265	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:620865	Ehlers-Danlos syndrome, classic-like, 3		HP:0000006	PMID:38433265	PCS					I	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0003577	PMID:26138117	PCS		2/2			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001176	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000582	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001355	PMID:26138117	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001272	OMIM:617011	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0002120	PMID:26138117	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001250	PMID:26138117	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0002066	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001252	PMID:26138117	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0045075	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0011220	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000316	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0003307	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0002119	PMID:26138117	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000218	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000256	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001763	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001249	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000358	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001166	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000494	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000472	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000098	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001344	OMIM:617011	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0002650	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001520	PMID:26138117	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000276	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001382	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001263	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000272	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0007074	OMIM:617011	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001519	PMID:26138117	PCS		2/2			P	HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0002808	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000426	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000007	PMID:26138117	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001833	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0002007	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000400	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000520	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0001334	PMID:26138117	PCS		1/2			P	HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000369	OMIM:617011	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000303	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:617011	Macrocephaly, dysmorphic facies, and psychomotor retardation		HP:0000325	PMID:26138117	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:221740	Deafness-Oligodontia syndrome		HP:0000007	OMIM:221740	IEA					I	HPO:iea[2009-02-17]
OMIM:221740	Deafness-Oligodontia syndrome		HP:0000677	OMIM:221740	IEA					P	HPO:iea[2009-02-17]
OMIM:221740	Deafness-Oligodontia syndrome		HP:0000699	OMIM:221740	IEA					P	HPO:iea[2009-02-17]
OMIM:221740	Deafness-Oligodontia syndrome		HP:0008527	OMIM:221740	IEA					P	HPO:iea[2009-02-17]
OMIM:615612	Developmental dysplasia of the hip 2		HP:0001385	PMID:23716478	PCS					P	HPO:nvasilevsky[2018-06-13]
OMIM:615612	Developmental dysplasia of the hip 2		HP:0002673	OMIM:615612	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615612	Developmental dysplasia of the hip 2		HP:0030838	OMIM:615612	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615612	Developmental dysplasia of the hip 2		HP:0008843	PMID:23716478	PCS		40%			P	HPO:nvasilevsky[2018-06-13]
OMIM:615612	Developmental dysplasia of the hip 2		HP:0000006	OMIM:615612	TAS					I	HPO:skoehler[2014-02-06]
OMIM:615612	Developmental dysplasia of the hip 2		HP:0001369	PMID:23716478	PCS					P	HPO:nvasilevsky[2018-06-13]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001298	PMID:29044765	PCS		3/3			P	HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0000571	PMID:29044765	PCS		1/3			P	HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001310	PMID:29044765	PCS		2/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001272	PMID:29044765	PCS		2/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0031629	PMID:29044765	PCS		3/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001263	PMID:29044765	PCS		3/3			P	HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001251	PMID:29044765	PCS		3/3			P	HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0002061	PMID:29044765	PCS		1/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0025190	PMID:29044765	PCS		3/3			P	HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0010602	PMID:29044765	PCS		1/1			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0010865	PMID:29044765	PCS		1/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0100710	PMID:29044765	PCS		1/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0000514	PMID:29044765	PCS		1/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0000007	PMID:29044765	PCS					I	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0000736	PMID:29044765	PCS		1/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0000666	PMID:29044765	PCS		3/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001337	PMID:29044765	PCS		1/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001348	PMID:29044765	PCS		2/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619028	Coenzyme Q10 deficiency, primary, 9		HP:0001336	PMID:29044765	PCS		2/3			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0004325	PMID:30503519	PCS		12/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0003510	PMID:30503519	PCS		12/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0001250	PMID:30503519	PCS		3/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000460	OMIM:618336	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0003593	PMID:30503519	PCS		1/15			C	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0004482	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0100255	PMID:30503519	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0002719	PMID:30503519	PCS		10/15			P	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000957	PMID:30503519	PCS		5/15			P	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0011463	PMID:30503519	PCS		4/15			C	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000938	PMID:30503519	PCS		4/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0008551	OMIM:618336	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0012190	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0030084	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000358	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0003623	PMID:30503519	PCS		4/15			C	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0003621	PMID:30503519	PCS		2/15			C	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000252	PMID:30503519	PCS		10/10			P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000054	OMIM:618336	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000475	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0003189	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0002650	PMID:30503519	PCS		3/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0011968	PMID:30503519	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0003581	PMID:30503519	PCS		4/15			C	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000470	OMIM:618336	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0033832	PMID:30503519	PCS		1/15			P	HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0012189	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0008244	PMID:30503519	PCS		12/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000007	PMID:30503519	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000964	PMID:30503519	PCS		3/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000824	PMID:30503519	PCS		5/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0002007	OMIM:618336	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0001511	PMID:30503519	PCS		15/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0008689	PMID:30503519	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000047	PMID:30503519	PCS		5/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000369	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0000347	PMID:30503519	PCS		1/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:618336	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency		HP:0002721	OMIM:618336	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000582	PMID:26843489	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000365	PMID:26843489	PCS		2/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000343	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000662	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000486	PMID:26843489	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0002188	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000463	PMID:26843489	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0001156	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0004322	PMID:26843489	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0001272	PMID:26843489	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0002120	PMID:26843489	PCS		2/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0001131	PMID:26843489	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0003593	PMID:26843489	PCS		3/3			C	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0012745	PMID:26843489	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0001270	PMID:26843489	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0010761	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0008070	PMID:26843489	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000639	PMID:26843489	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0011220	PMID:26843489	PCS		3/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0011120	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000219	PMID:26843489	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000455	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000510	PMID:26843489	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000358	PMID:26843489	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0005328	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0002135	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000750	PMID:26843489	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0002232	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0001321	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000490	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0001263	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0011003	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0012510	PMID:26843489	PCS		1/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0011304	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0012810	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000822	PMID:26843489	PCS		2/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000007	PMID:26843489	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000821	PMID:26843489	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0009836	PMID:26843489	PCS		2/3			P	HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000501	PMID:26843489	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000369	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:617763	Short stature, hearing loss, retinitis pigmentosa, and distinctive facies		HP:0000545	PMID:26843489	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-22]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0001254	PMID:12891654	PCS	HP:0003623	4/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002267	PMID:12891654	PCS		7/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:6000037	OMIM:608643	TAS					P	HPO:probinson[2024-01-06]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002020	PMID:12891654	PCS		9/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0003593	OMIM:608643	IEA					C	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:6001002	OMIM:608643	TAS					P	HPO:probinson[2024-08-04]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0100703	PMID:12891654	PCS		9/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000737	PMID:12891654	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000616	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000712	PMID:12891654	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0008872	PMID:12891654	PCS	HP:0003593	5/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000975	OMIM:608643	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002615	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0001742	PMID:12891654	PCS		8/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0005968	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002019	PMID:12891654	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0001347	PMID:12891654	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0200085	PMID:12891654	PCS		7/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0003785	PMID:12891654	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002014	PMID:12891654	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0005964	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0008936	PMID:12891654	PCS	HP:0003593	11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000473	PMID:12891654	PCS		7/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0003487	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0001266	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000271	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002451	PMID:12891654	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002374	PMID:12891654	PCS		11/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0001263	OMIM:608643	IEA					P	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0010553	PMID:12891654	PCS		11/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002509	PMID:12891654	PCS	HP:0003593	11/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000508	PMID:12891654	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000007	OMIM:608643	IEA					I	HPO:iea[2009-02-17]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0006543	PMID:12891654	PCS		2/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002305	PMID:12891654	PCS		11/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0002104	PMID:12891654	PCS		6/11			P	HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0001336	PMID:12891654	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-25]
OMIM:608643	Aromatic L-amino acid decarboxylase deficiency		HP:0000643	PMID:12891654	PCS		5/11			P	HPO:probinson[2021-06-25]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0001250	PMID:26607152	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0025267	OMIM:300942	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0003593	PMID:27245663	PCS					C	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0000280	PMID:27245663;PMID:26607152	PCS		6/13			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0012377	PMID:26607152	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0011463	PMID:27245663	PCS					C	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0033794	PMID:27245663	IEA		8/12			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0001548	PMID:26607152	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0000975	PMID:27245663;PMID:26607152	PCS		3/13			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0000956	PMID:27245663	PCS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0001423	PMID:27245663	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0002315	PMID:27245663;PMID:26607152	PCS		4/13			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0500001	OMIM:300942	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0000098	PMID:27245663	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0030269	PMID:27245663;PMID:25470569;PMID:26607152	PCS		27/27			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0002893	PMID:27245663;PMID:25470569	PCS		21/26			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0000870	PMID:27245663;PMID:25470569;PMID:26607152	PCS		24/27			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0002591	OMIM:300942	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0040075	PMID:26607152	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0010535	OMIM:300942	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0002829	PMID:27245663	PCS		1/12			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0002808	PMID:26607152	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0001714	OMIM:300942	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0000845	PMID:27245663;PMID:25470569;PMID:26607152	PCS		27/27			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0005616	OMIM:300942	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300942	Chromosome Xq26.3 duplication syndrome		HP:0000687	PMID:27245663	PCS		2/12			P	HPO:probinson[2021-05-08]
OMIM:173900	Polycystic kidneys		HP:0000083	OMIM:173900	IEA					P	HPO:iea[2009-02-17]
OMIM:173900	Polycystic kidneys		HP:0002253	OMIM:173900	IEA					P	HPO:iea[2009-02-17]
OMIM:173900	Polycystic kidneys		HP:0000822	OMIM:173900	TAS					P	HPO:probinson[2017-05-17]
OMIM:173900	Polycystic kidneys		HP:0001407	OMIM:173900	IEA					P	HPO:iea[2009-02-17]
OMIM:173900	Polycystic kidneys		HP:0000113	OMIM:173900	IEA					P	HPO:iea[2009-02-17]
OMIM:173900	Polycystic kidneys		HP:0001653	OMIM:173900	PCS		51/163			P	HPO:iea[2009-02-17]
OMIM:173900	Polycystic kidneys		HP:0007029	PMID:1513348	PCS		4/88			P	HPO:iea[2009-02-17]
OMIM:173900	Polycystic kidneys		HP:0000006	OMIM:173900	IEA					I	HPO:iea[2009-02-17]
OMIM:173900	Polycystic kidneys		HP:0001634	PMID:3419455	PCS		42/163			P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001254	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001993	OMIM:210210	IEA					P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001596	OMIM:210210	IEA					P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001992	OMIM:210210	IEA					P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0003234	PMID:17968484	PCS		3/5			P	HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001250	PMID:17968484	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0003353	OMIM:210210	IEA					P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001051	OMIM:210210	IEA					P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001252	OMIM:210210	IEA					P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0003593	PMID:17968484	PCS		4/5			C	HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001290	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0002919	OMIM:210210	IEA					P	HPO:skoehler[2018-10-08]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001508	PMID:17968484	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001943	OMIM:210210	IEA					P	HPO:skoehler[2018-10-08]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001987	PMID:17968484	PCS		2/5		HP:0012825	P	HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0003108	OMIM:210210	IEA					P	HPO:skoehler[2010-06-20]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001249	PMID:17968484	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001942	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001347	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0002179	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0003202	OMIM:210210	IEA					P	HPO:iea[2009-02-17]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0003621	PMID:17968484	PCS		1/5			C	HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0002013	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0011968	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001263	OMIM:210210	TAS		20/20			P	HPO:skoehler[2017-07-13];HPO:skoehler[2019-02-22]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0100021	PMID:17968484	PCS		1/5			P	HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0010911	PMID:17968484	PCS		2/5			P	HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0008281	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0000007	PMID:11181649	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:210210	3-Methylcrotonyl-CoA carboxylase 2 deficiency		HP:0001259	OMIM:210210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:306300	Granulomas, congenital cerebral		HP:0000707	OMIM:306300	IEA					P	HPO:iea[2009-02-17]
OMIM:306300	Granulomas, congenital cerebral		HP:0001939	OMIM:306300	IEA					P	HPO:iea[2009-02-17]
OMIM:306300	Granulomas, congenital cerebral		HP:0003811	OMIM:306300	IEA					C	HPO:iea[2009-02-17]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0002465	PMID:29576219	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0000582	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0031956	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0002151	PMID:29576219	PCS		2/2			P	HPO:probinson[2022-10-04];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0001252	PMID:29576219	PCS		2/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0001263	PMID:29576219	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0003593	PMID:29576219	PCS		2/2			C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0031964	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0100678	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0001508	PMID:29576219	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0000407	PMID:29576219	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0007340	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0001943	PMID:29576219	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0000007	PMID:29576219	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0012072	OMIM:617950	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0002315	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0020049	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0000369	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0001249	PMID:29576219	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0003326	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0003348	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:617950	Combined oxidative phosphorylation deficiency 36		HP:0003546	PMID:29576219	PCS		1/2			P	HPO:probinson[2022-10-04]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0003621	PMID:10974018	PCS		2/7			C	HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0003236	PMID:10974018	PCS		0/3			P	HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0011462	PMID:10974018	PCS		4/7			C	HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0003593	PMID:10974018	PCS		1/7			C	HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0001635	PMID:10974018	PCS		7/7			P	HPO:probinson[2013-02-23];HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0006673	PMID:10974018	PCS					P	HPO:probinson[2013-02-23]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0012664	PMID:10974018	PCS		5/5			P	HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0033755	PMID:10974018	PCS		5/5			P	HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0000006	PMID:10974018	PCS					I	HPO:probinson[2013-01-09]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0001645	PMID:10974018	PCS		4/7			P	HPO:probinson[2022-07-03]
OMIM:606685	Cardiomyopathy, dilated, 1L		HP:0001644	PMID:10974018	PCS					P	HPO:probinson[2013-02-23]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000286	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0003593	PMID:28191889	PCS					C	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0032895	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0012741	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:4000070	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0100033	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0001508	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000718	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0012450	PMID:28191889	PCS		2/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0002119	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0009765	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000256	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0001249	PMID:28191889	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000431	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0001762	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000750	PMID:28191889	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0001344	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0011968	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0002373	PMID:28191889	PCS		2/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0002033	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0001263	PMID:28191889	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0010511	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0031354	PMID:28191889	PCS		2/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0012810	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0100023	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0012520	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:4000076	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000729	PMID:28191889	PCS		5/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000403	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0001833	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000348	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0007018	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000028	PMID:28191889	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0000006	PMID:28191889	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0005338	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:617788	Intellectual developmental disorder, autosomal dominant 51		HP:0002028	PMID:28191889	PCS		1/7			P	HPO:probinson[2022-06-03]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0001320	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0001696	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0001640	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0005301	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0003363	PMID:36727596	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0030674	PMID:36727596	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0002198	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0003593	PMID:36727596	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0002092	PMID:36727596	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0011565	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0002093	PMID:36727596	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0011109	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0006270	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0034196	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0011682	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0012020	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0000007	PMID:36727596	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0001748	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0006532	PMID:36727596	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0001655	PMID:36727596	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620642	Ciliary dyskinesia, primary, 53		HP:0003623	PMID:36727596	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:302600	Spinocerebellar ataxia, X-linked 2		HP:0001251	OMIM:302600	IEA					P	HPO:iea[2009-02-17]
OMIM:302600	Spinocerebellar ataxia, X-linked 2		HP:0001417	OMIM:302600	IEA					I	HPO:iea[2009-02-17]
OMIM:302600	Spinocerebellar ataxia, X-linked 2		HP:0002071	OMIM:302600	IEA					P	HPO:iea[2009-02-17]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0009804	PMID:16628197	PCS		1/1			P	HPO:skoehler[2015-09-11];HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0002224	PMID:16628197	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0001036	OMIM:615821	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0030816	OMIM:615821	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0010783	OMIM:615821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0001808	OMIM:615821	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0008064	OMIM:615821	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0011463	PMID:16628197	PCS		1/1			C	HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0000989	OMIM:615821	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0008404	OMIM:615821	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0000982	PMID:16628197	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0001279	OMIM:615821	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0000006	PMID:16628197	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0004756	PMID:16628197	PCS		1/1			P	HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0001644	PMID:16628197	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0000962	PMID:16628197	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-18]
OMIM:615821	Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis		HP:0001820	OMIM:615821	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:206300	Anemia, nonspherocytic hemolytic, associated with abnormality of redcell membrane		HP:0001939	OMIM:206300	IEA					P	HPO:iea[2009-02-17]
OMIM:206300	Anemia, nonspherocytic hemolytic, associated with abnormality of redcell membrane		HP:0000007	OMIM:206300	IEA					I	HPO:iea[2009-02-17]
OMIM:206300	Anemia, nonspherocytic hemolytic, associated with abnormality of redcell membrane		HP:0001930	OMIM:206300	IEA					P	HPO:iea[2009-02-17]
OMIM:202600	Agenesis of cerebral white matter		HP:0200017	OMIM:202600	IEA					P	HPO:skoehler[2009-02-17]
OMIM:202600	Agenesis of cerebral white matter		HP:0000007	OMIM:202600	IEA					I	HPO:iea[2009-02-17]
OMIM:202600	Agenesis of cerebral white matter		HP:0001249	OMIM:202600	IEA					P	HPO:iea[2009-02-17]
OMIM:608864	Orofacial cleft 6, susceptibility to		HP:0000175	OMIM:608864	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608864	Orofacial cleft 6, susceptibility to		HP:0010982	OMIM:608864	TAS					I	HPO:skoehler[2013-03-12]
OMIM:608864	Orofacial cleft 6, susceptibility to		HP:0003745	OMIM:608864	TAS					I	HPO:skoehler[2015-12-30]
OMIM:608864	Orofacial cleft 6, susceptibility to		HP:0000204	OMIM:608864	TAS					P	HPO:skoehler[2009-02-17]
OMIM:608864	Orofacial cleft 6, susceptibility to		HP:0000006	OMIM:608864	IEA					I	HPO:skoehler[2019-04-18]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002982	PMID:10377013	PCS		2/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0003510	PMID:10377013	PCS		4/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0007517	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000365	PMID:10377013	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002980	PMID:10377013	PCS		2/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0001250	PMID:10377013	PCS		1/4			P	HPO:skoehler[2015-07-26]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002384	PMID:10377013	PCS		1/3			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0010609	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002020	PMID:10377013	PCS		1/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002938	PMID:10377013	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000238	PMID:10377013	PCS		3/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000956	PMID:10377013	PCS		3/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0001249	PMID:10377013	PCS		2/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000131	PMID:10377013	PCS		1/3	FEMALE		P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002079	PMID:10377013	PCS		3/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002871	PMID:10377013	PCS		1/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0001582	PMID:10377013	PCS		1/4			P	HPO:skoehler[2018-10-08]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0001263	PMID:10377013	PCS		3/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0011800	PMID:10377013	PCS		1/4			P	HPO:skoehler[2015-07-26]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0011003	PMID:10377013	PCS		1/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0100777	PMID:10377013	PCS		1/3			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000926	PMID:10377013	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000403	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000006	PMID:10053006	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0003577	PMID:10377013	PCS		4/4			C	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0008905	PMID:10377013	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0001355	PMID:10377013	PCS		1/4			P	HPO:skoehler[2015-07-26]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0003498	PMID:10377013	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000260	PMID:10377013	PCS		2/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000020	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000858	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002878	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000774	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000256	PMID:10377013	PCS		2/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0001623	PMID:10377013	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002677	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0000577	PMID:10377013	PCS		1/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0003027	PMID:10377013	PCS		1/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0030049	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002098	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002092	PMID:10377013	PCS		1/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0005280	PMID:10377013	PCS		1/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002808	PMID:10377013	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002607	PMID:10377013	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0001635	PMID:10377013	PCS		1/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0003811	PMID:10377013	PCS		1/4			C	HPO:probinson[2023-02-11]
OMIM:616482	Achondroplasia, severe, with developmental delay and acanthosis nigricans		HP:0002007	PMID:10377013	PCS		1/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0000286	OMIM:250620	TAS					P	HPO:skoehler[2015-11-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001254	PMID:17160907	PCS		1/1			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0000486	OMIM:250620	TAS					P	HPO:skoehler[2015-11-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0003355	OMIM:250620	IEA					P	HPO:skoehler[2010-06-20]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001310	PMID:17160907	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001332	OMIM:250620	TAS					P	HPO:skoehler[2015-04-05]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001250	OMIM:250620	TAS					P	HPO:skoehler[2015-04-05]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001274	PMID:17160907	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001252	PMID:17160907	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001251	PMID:17160907	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0003593	PMID:17160907	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001270	PMID:17160907	PCS		1/1			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:6000215	OMIM:250620	TAS					P	HPO:probinson[2024-02-09]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001508	PMID:17160907	PCS		1/1			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0000639	PMID:17160907	PCS		1/1			P	HPO:skoehler[2015-11-15];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0000737	PMID:17160907	PCS		1/1			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0003468	OMIM:250620	TAS					P	HPO:skoehler[2013-05-29]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0002599	PMID:17160907	PCS		1/1			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0002078	PMID:17160907	PCS		1/1			P	HPO:probinson[2022-12-15];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0002376	PMID:17160907	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0011968	OMIM:250620	TAS					P	HPO:skoehler[2015-04-05]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001263	OMIM:250620	TAS					P	HPO:skoehler[2015-04-05]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0000925	OMIM:250620	IEA					P	HPO:skoehler[2010-06-20]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001636	PMID:17160907	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0000007	PMID:17160907	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-15]
OMIM:250620	3-hydroxyisobutryl-CoA hydrolase deficiency		HP:0001336	OMIM:250620	TAS					P	HPO:skoehler[2015-04-05]
OMIM:619799	Spermatogenic failure 66		HP:0003251	PMID:31985809	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:619799	Spermatogenic failure 66		HP:0011462	PMID:31985809	PCS		1/1			C	HPO:probinson[2022-05-10]
OMIM:619799	Spermatogenic failure 66		HP:0000007	PMID:31985809	PCS					I	HPO:probinson[2022-05-10]
OMIM:619799	Spermatogenic failure 66		HP:0012205	PMID:31985809	PCS		1/1			P	HPO:probinson[2022-05-10]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000220	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000343	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000463	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0003593	PMID:35642635	PCS		2/2			C	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0030319	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0001508	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000419	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000338	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000678	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000219	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0002714	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0003327	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000411	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0001324	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000358	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0002650	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000430	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0001761	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0011805	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0008081	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0030822	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0011094	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000007	PMID:35642635	PCS					I	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0002705	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000347	PMID:35642635	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0000369	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:619941	Carey-Fineman-Ziter syndrome 2		HP:0001611	PMID:35642635	PCS		1/2			P	HPO:probinson[2022-08-04]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0000660	PMID:12783430	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0002155	PMID:12783430;PMID:213719	PCS		12/12			P	HPO:probinson[2021-07-02];HPO:probinson[2021-07-02];HPO:probinson[2021-07-02];HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0001013	PMID:213719;PMID:3944267	PCS		1/10			P	HPO:probinson[2021-07-02];HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0003124	PMID:12783430	PCS		2/2			P	HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0002240	PMID:12783430;PMID:213719;PMID:3944267	PCS		4/6			P	HPO:probinson[2021-07-02];HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0033983	PMID:213719;PMID:6547689;PMID:3944267	PCS		11/11			P	HPO:probinson[2021-07-16]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0000007	PMID:12783430	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0001733	PMID:213719	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0001744	PMID:3944267	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-02]
OMIM:207750	Apolipoprotein C-II deficiency		HP:0012238	PMID:213719	PCS		10/10			P	HPO:probinson[2021-07-02];HPO:probinson[2021-07-02];HPO:probinson[2021-07-02]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0007703	OMIM:251270	TAS					P	HPO:probinson[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000252	OMIM:251270	IEA					P	HPO:iea[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0001000	OMIM:251270	IEA					P	HPO:skoehler[2010-06-20]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000340	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0002059	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0003577	OMIM:251270	TAS					C	HPO:skoehler[2015-12-30]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000541	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0004322	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0001321	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0001250	OMIM:251270	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0001263	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0008052	OMIM:251270	TAS					P	HPO:probinson[2015-07-19]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000518	OMIM:251270	IEA					P	HPO:iea[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000639	OMIM:251270	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000007	OMIM:251270	IEA					I	HPO:iea[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000568	OMIM:251270	IEA					P	HPO:iea[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000505	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0007731	PMID:11146476	PCS					P	HPO:probinson[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000543	OMIM:251270	IEA					P	HPO:iea[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0001302	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0001249	OMIM:251270	IEA					P	HPO:iea[2009-02-17]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0000556	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1		HP:0009879	OMIM:251270	TAS					P	HPO:skoehler[2015-02-22]
OMIM:601868	Deafness, autosomal dominant nonsyndromic sensorineural 13		HP:0000407	OMIM:601868	TAS	HP:0003577				P	HPO:probinson[2013-04-12]
OMIM:601868	Deafness, autosomal dominant nonsyndromic sensorineural 13		HP:0000006	OMIM:601868	IEA					I	HPO:iea[2009-02-17]
OMIM:610965	XFE progeroid syndrome		HP:0003510	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0008209	PMID:29105242	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000365	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0003079	PMID:17183314	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000083	PMID:17183314	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0003073	PMID:17183314	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0001508	PMID:29105242	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000958	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0006297	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000618	PMID:29105242	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0007485	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0002119	PMID:29105242	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000559	PMID:29105242	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0001620	PMID:29105242	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0002910	PMID:17183314	PCS		1/1		HP:0012825	P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0007843	PMID:17183314	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000336	PMID:29105242;PMID:17183314	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0002311	PMID:29105242	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000275	PMID:29105242	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000252	PMID:29105242;PMID:17183314	PCS		2/2			P	HPO:probinson[2013-01-09];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0002650	PMID:17183314	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0004334	PMID:29105242	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000992	PMID:17183314	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0001761	PMID:29105242	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0001541	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000490	PMID:29105242	PCS		2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000093	PMID:17183314	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0011421	PMID:17183314	PCS		1/1			C	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0006480	PMID:29105242	PCS		1/1			P	HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0007495	PMID:29105242;PMID:17183314	PCS		2/2			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000822	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000007	PMID:17183314	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000505	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000648	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0000444	PMID:17183314	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-15]
OMIM:610965	XFE progeroid syndrome		HP:0004326	PMID:17183314	PCS		1/1			P	HPO:probinson[2013-04-01];HPO:probinson[2022-03-15]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000286	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000263	OMIM:200995	IEA					P	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000582	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0002983	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0002089	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0005210	OMIM:200995	IEA					P	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0001395	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0003196	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0002240	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0001072	OMIM:200995	IEA					P	HPO:skoehler[2018-10-08]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000316	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0001748	OMIM:200995	IEA					P	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000377	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0001363	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0001541	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0001162	OMIM:200995	IEA					P	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000470	OMIM:200995	TAS					P	HPO:probinson[2012-09-18]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0004790	OMIM:200995	IEA					P	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0100732	OMIM:200995	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000800	OMIM:200995	IEA					P	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000007	OMIM:200995	IEA					I	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0001539	OMIM:200995	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0006544	OMIM:200995	IEA					P	HPO:iea[2009-02-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000105	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200995	Acrocephalopolydactylous dysplasia		HP:0000369	OMIM:200995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000341	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0003477	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001276	PMID:23911318	PCS		7/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0002169	PMID:23911318	PCS		6/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0003577	PMID:23911318	PCS		3/8			C	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000486	PMID:23911318	PCS		1/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000188	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001332	PMID:23911318	PCS		3/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0002120	OMIM:615809	TAS					P	HPO:skoehler[2014-06-24]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001250	PMID:23911318	PCS		6/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0003593	PMID:23911318	PCS		5/8			C	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0012110	PMID:23911318	PCS		8/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0100704	PMID:23911318	PCS		5/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000737	PMID:23911318	PCS		8/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0006970	PMID:23911318	PCS		1/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0002119	PMID:23911318	PCS		6/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000158	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000377	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001249	PMID:23911318	PCS		8/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001347	PMID:23911318	PCS		8/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0008936	PMID:23911318	PCS		2/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000297	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000494	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0002015	PMID:23911318	PCS		7/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001344	PMID:23911318	PCS		6/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0002079	PMID:23911318	PCS		8/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001321	PMID:23911318	PCS		8/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001263	PMID:23911318	PCS		8/8		HP:0012829	P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0002151	PMID:23911318	PCS		0/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0005484	PMID:23911318	PCS		8/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0011800	OMIM:615809	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0012434	PMID:23911318	PCS		8/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0025405	PMID:23911318	PCS		7/8			P	HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000007	PMID:23911318	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0000648	PMID:23911318	PCS		4/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:615809	Pontocerebellar hypoplasia, type 9		HP:0001257	PMID:23911318	PCS		8/8			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-01-18]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000483	PMID:25078763	PCS		2/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002045	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002540	PMID:25078763	PCS		2/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000486	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000540	PMID:25078763	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0004322	OMIM:618493	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0001250	PMID:25078763	PCS		4/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0003273	PMID:25078763	PCS		4/4			P	HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0003593	PMID:25078763	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0001290	PMID:25078763	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000280	PMID:25078763	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0011185	PMID:25078763	PCS		1/6			P	HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0006094	PMID:25078763	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0100704	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0011220	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0012471	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002317	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0001945	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0006532	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002857	PMID:25078763	PCS		6/6			P	HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002019	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000577	PMID:25078763	PCS		5/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000252	OMIM:618493	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002650	PMID:25078763	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000496	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0031936	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002791	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0001263	PMID:25078763	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0011203	PMID:25078763	PCS		1/6			P	HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0004370	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0005280	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0010535	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002808	PMID:25078763	PCS		2/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0012043	PMID:25078763	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000646	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000007	PMID:25078763	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000648	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0002987	PMID:25078763	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000303	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0000545	OMIM:618493	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618493	Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities		HP:0001513	PMID:25078763	PCS		5/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-04-16]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0003477	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0006989	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0003236	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000486	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0001250	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0001274	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000639	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0011463	PMID:34054129	PCS		6/7			C	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000378	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0007766	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0009748	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0003623	PMID:34054129	PCS		1/7			C	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000252	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000076	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0030048	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0002395	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0001263	PMID:34054129	PCS		6/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000691	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000470	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0005280	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0012583	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0012520	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000729	PMID:34054129	PCS		3/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000508	PMID:34054129	PCS		2/7			P	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0000007	PMID:34054129	PCS					I	HPO:probinson[2022-08-23]
OMIM:619955	Dworschak-Punetha neurodevelopmental syndrome		HP:0005338	PMID:34054129	PCS		1/7			P	HPO:probinson[2022-08-23];HPO:probinson[2022-08-23]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0001056	PMID:9540991	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0001047	PMID:9540991	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0000992	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0002750	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0002384	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0001030	PMID:9540991;PMID:8673113	PCS		2/2			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0001250	PMID:9540991	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0001263	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0010049	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0011003	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0012187	PMID:9540991	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0034283	PMID:9540991	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0100699	PMID:9540991	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0009381	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0008066	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0011463	PMID:9540991	PCS		1/1			C	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0012043	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0000007	PMID:8673113	PCS					I	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0000763	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0001249	PMID:9540991	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0003623	PMID:8673113	PCS		1/1			C	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0200041	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620483	Variegate porphyria, childhood-onset		HP:0000962	PMID:8673113	PCS		1/1			P	HPO:probinson[2024-12-03]
OMIM:619202	Spermatogenic failure 52		HP:0003251	PMID:33508233	PCS		4/4	MALE		P	HPO:probinson[2021-03-14]
OMIM:619202	Spermatogenic failure 52		HP:0011462	PMID:33508233	PCS		4/4			C	HPO:probinson[2022-08-26]
OMIM:619202	Spermatogenic failure 52		HP:0000007	PMID:33508233	PCS					I	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:619202	Spermatogenic failure 52		HP:0000027	PMID:33508233	PCS		2/2	MALE		P	HPO:probinson[2021-03-14];HPO:probinson[2021-03-14]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001397	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0000252	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0003256	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001250	PMID:22607940	PCS					P	HPO:probinson[2015-05-08]
OMIM:615438	Infantile liver failure syndrome 1		HP:0000293	OMIM:615438	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001263	PMID:22607940	PCS					P	HPO:probinson[2015-05-08]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001252	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0002240	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0010511	OMIM:615438	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001290	OMIM:615438	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615438	Infantile liver failure syndrome 1		HP:0002194	OMIM:615438	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001508	PMID:22607940	PCS					P	HPO:probinson[2015-05-08]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001903	PMID:22607940	PCS					P	HPO:probinson[2015-05-08]
OMIM:615438	Infantile liver failure syndrome 1		HP:0000407	OMIM:615438	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0000007	PMID:22607940	PCS					I	HPO:probinson[2015-05-08]
OMIM:615438	Infantile liver failure syndrome 1		HP:0100807	OMIM:615438	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0006554	PMID:22607940	PCS					P	HPO:probinson[2015-05-08]
OMIM:615438	Infantile liver failure syndrome 1		HP:0002007	OMIM:615438	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0002910	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0001972	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:615438	Infantile liver failure syndrome 1		HP:0003128	OMIM:615438	TAS					P	HPO:skoehler[2015-08-02]
OMIM:188740	Tibia, hypoplasia or aplasia of, with polydactyly		HP:0001199	PMID:19847792	PCS		11/13			P	HPO:probinson[2022-03-20]
OMIM:188740	Tibia, hypoplasia or aplasia of, with polydactyly		HP:0003577	PMID:19847792	PCS		13/13			C	HPO:probinson[2022-03-20]
OMIM:188740	Tibia, hypoplasia or aplasia of, with polydactyly		HP:0100258	PMID:19847792	PCS		12/13			P	HPO:probinson[2022-03-20]
OMIM:188740	Tibia, hypoplasia or aplasia of, with polydactyly		HP:0009556	PMID:19847792	PCS					P	HPO:skoehler[2013-10-22];HPO:probinson[2022-03-20]
OMIM:188740	Tibia, hypoplasia or aplasia of, with polydactyly		HP:0005736	PMID:19847792	PCS					P	HPO:probinson[2022-03-20]
OMIM:188740	Tibia, hypoplasia or aplasia of, with polydactyly		HP:0010503	PMID:19847792	PCS		1/13			P	HPO:probinson[2022-03-20]
OMIM:188740	Tibia, hypoplasia or aplasia of, with polydactyly		HP:0000006	PMID:19847792	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-20]
OMIM:612431	Deafness, autosomal dominant 27		HP:0000407	PMID:18279434	PCS	HP:0003621				P	HPO:probinson[2019-01-16]
OMIM:612431	Deafness, autosomal dominant 27		HP:0000006	PMID:18279434	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-01-16]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002540	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002188	PMID:25930971	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001250	OMIM:616657	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001252	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0003593	PMID:25930971	PCS		2/2			C	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0033725	PMID:25930971	PCS		2/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0000737	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0000752	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001249	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001348	PMID:25930971	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001347	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0000253	OMIM:616657	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002510	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0000252	PMID:25930971	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002059	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001344	PMID:25930971	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002079	OMIM:616657	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0003487	PMID:25930971	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002197	PMID:25930971	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001263	PMID:25930971	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0011448	PMID:25930971	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0000007	PMID:25930971	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002307	PMID:25930971	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0006466	PMID:25930971	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0001257	PMID:25930971	PCS		2/2			P	HPO:probinson[2022-09-25]
OMIM:616657	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly		HP:0002500	PMID:25930971	PCS		1/2			P	HPO:probinson[2022-09-25]
OMIM:128290	Ear antitragus, tag at base of		HP:0000598	OMIM:128290	IEA					P	HPO:iea[2009-02-17]
OMIM:128290	Ear antitragus, tag at base of		HP:0000006	OMIM:128290	IEA					I	HPO:iea[2009-02-17]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000054	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0001363	PMID:22634751	PCS		3/11			P	HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0002750	PMID:22634751	PCS		10/11			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0001263	OMIM:614732	TAS		HP:0040283			P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0003196	PMID:22634751	PCS		11/11			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0002150	PMID:22634751	PCS		4/5			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0003072	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0100255	PMID:22634751	PCS		8/10			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0005280	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0011220	PMID:22634751	PCS		11/11			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000938	PMID:22634751	PCS		3/3			P	HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000835	PMID:22634751	PCS	HP:0003577	11/11			P	HPO:skoehler[2013-06-06];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000824	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0008897	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0002656	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0001511	PMID:22634751	PCS		11/11			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000047	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000256	OMIM:614732	TAS		HP:0040283			P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000006	PMID:22634751	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2022-09-29]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000028	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:614732	Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasiacongenita, and genital anomalies		HP:0000369	OMIM:614732	TAS					P	HPO:skoehler[2013-01-11]
OMIM:618108	Immunodeficiency 57		HP:0002014	PMID:30026316	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0005403	PMID:30026316	PCS		3/4			P	HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0004313	PMID:30026316	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0002037	PMID:30026316	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0006528	PMID:30026316	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0410297	PMID:30026316	PCS		1/4			P	HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0002110	PMID:30026316	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0003593	PMID:30026316	PCS		1/4			C	HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0005263	PMID:30026316	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0010976	PMID:30026316	PCS		1/4			P	HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0001508	PMID:30026316	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0000007	PMID:30026316	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0000988	PMID:30026316	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0002205	PMID:30026316	PCS		3/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0009789	PMID:30026316	PCS		3/4			P	HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0040218	PMID:30026316	PCS		3/4			P	HPO:probinson[2021-02-20];HPO:probinson[2021-02-20]
OMIM:618108	Immunodeficiency 57		HP:0003623	PMID:30026316	PCS		3/4			C	HPO:probinson[2021-02-20]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000286	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0010804	OMIM:309580	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000046	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0004322	OMIM:309580	TAS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000089	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001250	OMIM:309580	TAS		35%			P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0010808	OMIM:309580	TAS					P	HPO:skoehler[2012-10-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0010806	OMIM:309580	PCS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0002020	OMIM:309580	PCS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000280	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000316	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0009466	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0002857	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001566	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000158	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000752	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0008734	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001884	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001763	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0002019	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000358	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000451	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0002751	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000054	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000252	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0002750	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0011800	OMIM:309580	TAS					P	HPO:skoehler[2013-11-28]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001182	OMIM:309580	TAS					P	HPO:probinson[2013-04-09]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001419	PMID:8630485	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-21]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000407	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000648	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0002307	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000047	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000369	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000341	OMIM:309580	PCS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0008947	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000582	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000188	OMIM:309580	TAS					P	HPO:skoehler[2013-08-10]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001156	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000463	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001871	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0008551	OMIM:309580	PCS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000219	OMIM:309580	TAS					P	HPO:skoehler[2013-06-04]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0006895	OMIM:309580	PCS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000218	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0030084	OMIM:309580	IEA					P	HPO:skoehler[2018-10-08]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000179	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000135	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001347	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000577	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000154	OMIM:309580	PCS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0005326	OMIM:309580	TAS					P	HPO:skoehler[2017-07-13]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000076	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000431	OMIM:309580	TAS					P	HPO:probinson[2012-05-01]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001762	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0002013	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000194	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000470	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000272	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0005280	OMIM:309580	TAS					P	HPO:probinson[2012-05-01]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000749	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000508	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000268	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001238	OMIM:309580	TAS					P	HPO:probinson[2013-04-09]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0001513	OMIM:309580	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000347	OMIM:309580	PCS					P	HPO:probinson[2012-03-26]
OMIM:309580	Intellectual disability-hypotonic facies syndrome, X-linked		HP:0000028	OMIM:309580	IEA					P	HPO:iea[2009-02-17]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0001265	PMID:33559681	PCS		8/16			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0003401	PMID:33559681	PCS		3/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0001762	PMID:33559681	PCS		6/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0001761	PMID:33559681	PCS		11/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0008959	PMID:33559681	PCS		8/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0001371	PMID:33559681	PCS		9/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0003691	PMID:33559681	PCS		2/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0001252	PMID:33559681	PCS		1/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0010830	PMID:33559681	PCS		3/15			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0009053	PMID:33559681	PCS		15/16			P	HPO:probinson[2021-06-26]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0011463	PMID:33559681	PCS					C	HPO:probinson[2021-05-14];HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0007210	PMID:33559681	PCS		10/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0007002	PMID:33559681	PCS		15/15			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0009027	PMID:33559681	PCS		9/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0000007	PMID:33559681	PCS					I	HPO:probinson[2021-05-14];HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0001308	PMID:33559681	PCS		2/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0002359	PMID:33559681	PCS		6/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0003326	PMID:33559681	PCS		7/17			P	HPO:probinson[2021-05-14]
OMIM:619216	Neuropathy, hereditary motor, with myopathic features		HP:0003458	PMID:33559681	PCS		3/12			P	HPO:probinson[2021-05-14]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0004325	OMIM:613075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000286	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0000343	PMID:20424861;PMID:30769224	PCS		4/4			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001596	OMIM:613075	IEA					P	HPO:skoehler[2015-01-19]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001156	OMIM:613075	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0004322	OMIM:613075	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001252	PMID:20424861	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0003593	PMID:30769224	PCS		1/1			C	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0003010	PMID:20424861	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000280	PMID:30769224	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0045075	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0008070	PMID:19631308;PMID:20424861	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000939	PMID:19631308	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000815	OMIM:613075	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0040079	PMID:19631308;PMID:20424861	PCS		5/6			P	HPO:probinson[2022-05-08];HPO:skoehler[2014-11-26];HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0012471	PMID:20424861;PMID:30769224	PCS		4/4			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0012472	PMID:19631308	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000954	OMIM:613075	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000978	PMID:20424861;PMID:30769224	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000218	PMID:19631308;PMID:20424861	PCS		4/6			P	HPO:probinson[2022-05-08];HPO:skoehler[2012-11-18];HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0000977	PMID:20424861	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0007204	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000212	PMID:19631308;PMID:20424861;PMID:30769224	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001620	PMID:19631308;PMID:20424861	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000256	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001763	PMID:20424861;PMID:30769224	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000974	PMID:20424861;PMID:30769224	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000973	OMIM:613075	IEA					P	HPO:skoehler[2015-07-29]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000494	PMID:19631308;PMID:20424861;PMID:30769224	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0002650	PMID:19631308;PMID:20424861;PMID:30769224	PCS		6/7			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08];HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000431	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001382	PMID:20424861;PMID:30769224	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0002110	OMIM:613075	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001582	PMID:19631308;PMID:20424861	PCS		6/6			P	HPO:probinson[2022-05-08];HPO:skoehler[2018-10-08];HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0011003	PMID:20424861	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0012378	PMID:20424861	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0011107	PMID:19631308	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0100540	PMID:19631308;PMID:20424861;PMID:30769224	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0012520	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0008064	PMID:19631308;PMID:20424861;PMID:30769224	PCS		1/7			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08];HPO:probinson[2022-05-08];HPO:skoehler[2012-11-18];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0008661	PMID:19631308	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0000767	PMID:20424861	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0001537	PMID:19631308;PMID:20424861;PMID:30769224	PCS		4/7			P	HPO:probinson[2022-05-08];HPO:skoehler[2012-11-18];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000007	PMID:19631308	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000348	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000028	OMIM:613075	TAS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-05-08]
OMIM:613075	Macrocephaly, alopecia, cutis laxa, and scoliosis		HP:0000347	PMID:30769224	PCS		1/1			P	HPO:probinson[2022-05-08]
OMIM:613075	Macs syndrome		HP:0004942	PMID:19631308	PCS		1/3		HP:0012825	P	HPO:probinson[2022-05-08]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001254	PMID:29478781	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001298	PMID:29478781	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0002069	PMID:29478781	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0003236	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001993	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0000750	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0004322	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0003201	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0011925	PMID:29478781	PCS		2/2			P	HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001263	PMID:29478781	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0002141	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0031962	PMID:29478781	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0011463	PMID:29478781	PCS		1/2			C	HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001943	PMID:29478781	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001987	PMID:29478781	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0000007	PMID:29478781	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0006466	PMID:29478781	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001324	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0003623	PMID:29478781	PCS		1/2			C	HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0003128	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0003546	PMID:29478781	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0001644	PMID:29478781	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618120	Mitochondrial complex V (ATP synthase) deficiency nuclear type 5		HP:0003535	PMID:29478781	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:617213	Sedoheptulokinase deficiency		HP:0025157	PMID:25647543	PCS		2/2			P	HPO:probinson[2017-05-28]
OMIM:617213	Sedoheptulokinase deficiency		HP:0000007	PMID:25647543	PCS		2/2			I	HPO:probinson[2017-05-28]
OMIM:156000	Meniere disease		HP:0000365	OMIM:156000	IEA					P	HPO:iea[2009-02-17]
OMIM:156000	Meniere disease		HP:0002321	OMIM:156000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:156000	Meniere disease		HP:0000360	OMIM:156000	TAS					P	HPO:skoehler[2014-11-26]
OMIM:156000	Meniere disease		HP:0003829	OMIM:156000	TAS					I	HPO:skoehler[2015-12-30]
OMIM:156000	Meniere disease		HP:0000006	OMIM:156000	IEA					I	HPO:iea[2009-02-17]
OMIM:601471	Facial paresis, hereditary congenital, 1		HP:0010628	PMID:8872479	PCS					P	HPO:lccarmody[2018-10-18]
OMIM:601471	Facial paresis, hereditary congenital, 1		HP:0012507	OMIM:601471	TAS					P	HPO:lccarmody[2018-10-18]
OMIM:601471	Facial paresis, hereditary congenital, 1		HP:0008000	PMID:8872479	PCS					P	HPO:lccarmody[2018-10-18]
OMIM:601471	Facial paresis, hereditary congenital, 1		HP:0003680	OMIM:601471	IEA					C	HPO:iea[2009-02-17]
OMIM:601471	Facial paresis, hereditary congenital, 1		HP:0000006	OMIM:601471	IEA					I	HPO:iea[2009-02-17]
OMIM:601317	Deafness, autosomal dominant nonsyndromic sensorineural 11		HP:0008619	OMIM:601317	TAS					P	HPO:probinson[2009-02-17]
OMIM:601317	Deafness, autosomal dominant nonsyndromic sensorineural 11		HP:0001751	OMIM:601317	TAS					P	HPO:probinson[2013-12-15]
OMIM:601317	Deafness, autosomal dominant nonsyndromic sensorineural 11		HP:0002321	OMIM:601317	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601317	Deafness, autosomal dominant nonsyndromic sensorineural 11		HP:0000006	OMIM:601317	TAS					I	HPO:probinson[2009-02-17]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0002510	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0003577	PMID:31412107	PCS					C	HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0012695	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0002540	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0001344	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0001332	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0002134	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0000007	PMID:31412107	PCS					I	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0008872	PMID:31412107	PCS	HP:0003593	2/2			P	HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0011344	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:618646	Diencephalic-mesencephalic junction dysplasia syndrome 2		HP:0040326	PMID:31412107	PCS		2/2			P	HPO:probinson[2020-06-28];HPO:probinson[2020-06-28]
OMIM:609993	Osteosclerosis - ichthyosis - premature ovarian failure		HP:0008209	OMIM:609993	TAS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-07-14]
OMIM:609993	Osteosclerosis - ichthyosis - premature ovarian failure		HP:0008064	OMIM:609993	TAS					P	HPO:probinson[2021-07-14]
OMIM:609993	Osteosclerosis - ichthyosis - premature ovarian failure		HP:0012514	OMIM:609993	TAS					P	HPO:probinson[2021-07-14]
OMIM:609993	Osteosclerosis - ichthyosis - premature ovarian failure		HP:0031485	OMIM:609993	TAS					P	HPO:probinson[2021-07-14]
OMIM:609993	Osteosclerosis - ichthyosis - premature ovarian failure		HP:0005746	OMIM:609993	TAS					P	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:609993	Osteosclerosis - ichthyosis - premature ovarian failure		HP:0008724	OMIM:609993	TAS		3/3			P	HPO:probinson[2021-07-14]
OMIM:617575	Nephrotic syndrome, type 14		HP:0003774	PMID:28165343	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0003676	PMID:28165343	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000486	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000100	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001250	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001251	PMID:28165343	PCS		2/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0003593	PMID:28165343	PCS		6/8			C	HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001290	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0003073	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0031266	PMID:28165343	PCS					P	HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0012588	PMID:28165343	PCS		5/8			P	HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0012574	PMID:28165343	PCS		2/4			P	HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0011463	PMID:28165343	PCS		1/8			C	HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001943	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001888	PMID:28165343	PCS		2/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000953	PMID:28165343	PCS		8/8			P	HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001967	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000135	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001268	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000252	OMIM:617575	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000054	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0003621	PMID:28165343	PCS		1/8			C	HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0002155	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0002376	PMID:28165343	PCS		1/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000097	PMID:28165343	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0001263	PMID:28165343	PCS		3/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000093	PMID:28165343	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0008064	PMID:28165343	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000969	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000407	PMID:28165343	PCS		2/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000508	OMIM:617575	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617575	Nephrotic syndrome, type 14		HP:0009830	OMIM:617575	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000007	PMID:28165343	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000821	PMID:28165343	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000846	PMID:28165343	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:617575	Nephrotic syndrome, type 14		HP:0000028	PMID:28165343	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-06]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002069	PMID:23297359	PCS		3/4			P	HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0003676	PMID:23297359	PCS					C	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001272	PMID:23297359	PCS		1/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002120	PMID:23297359	PCS		2/4			P	HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001250	OMIM:615362	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002066	PMID:23297359	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001251	PMID:23297359	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0000716	PMID:23297359	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0011462	PMID:23297359	PCS		4/4			C	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0000712	PMID:23297359	PCS		1/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002119	PMID:23297359	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001268	PMID:23297359	PCS		4/4		HP:0003676	P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001347	PMID:23297359	PCS		1/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002476	OMIM:615362	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001289	PMID:23297359	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0003487	OMIM:615362	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001260	PMID:23297359	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002071	OMIM:615362	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0000726	PMID:23297359	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002506	PMID:23297359	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0000007	PMID:23297359	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0002529	PMID:23297359	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0007359	PMID:23297359	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001337	PMID:23297359	PCS		3/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-11]
OMIM:615362	Ceroid lipofuscinosis, neuronal, 13		HP:0001336	OMIM:615362	TAS					P	HPO:skoehler[2015-12-30]
OMIM:261600	Phenylketonuria		HP:0002686	OMIM:261600	IEA					H	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0001250	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0002286	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0034458	OMIM:261600	TAS					P	HPO:probinson[2022-12-18]
OMIM:261600	Phenylketonuria		HP:0100324	OMIM:261600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261600	Phenylketonuria		HP:0000518	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000716	OMIM:261600	TAS					P	HPO:skoehler[2015-12-30]
OMIM:261600	Phenylketonuria		HP:0000958	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000737	OMIM:261600	TAS					P	HPO:skoehler[2012-11-20]
OMIM:261600	Phenylketonuria		HP:0000718	OMIM:261600	TAS					P	HPO:skoehler[2012-11-20]
OMIM:261600	Phenylketonuria		HP:0000739	OMIM:261600	TAS					P	HPO:skoehler[2012-11-20]
OMIM:261600	Phenylketonuria		HP:0000635	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000752	OMIM:261600	TAS					P	HPO:skoehler[2012-11-20]
OMIM:261600	Phenylketonuria		HP:6000281	PMID:466810	PCS	HP:0003577	12/12			P	HPO:probinson[2024-02-27]
OMIM:261600	Phenylketonuria		HP:0002514	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0001249	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0001347	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000252	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0410066	PMID:22626821;PMID:19551947	PCS		20/20			P	HPO:NicoleVasilevsky[2018-02-23];HPO:NicoleVasilevsky[2018-03-02]
OMIM:261600	Phenylketonuria		HP:0005982	OMIM:261600	PCS					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000709	OMIM:261600	TAS					P	HPO:skoehler[2012-11-20]
OMIM:261600	Phenylketonuria		HP:0100610	OMIM:261600	TAS					H	HPO:skoehler[2012-11-20]
OMIM:261600	Phenylketonuria		HP:0000007	OMIM:261600	IEA					I	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000964	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000722	OMIM:261600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:261600	Phenylketonuria		HP:0004923	OMIM:261600	PCS					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0007018	OMIM:261600	TAS					P	HPO:skoehler[2012-11-20]
OMIM:261600	Phenylketonuria		HP:0007513	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0004920	OMIM:261600	IEA					P	HPO:iea[2009-02-17]
OMIM:261600	Phenylketonuria		HP:0000742	OMIM:261600	TAS					P	HPO:skoehler[2012-11-20]
OMIM:613707	Leopard syndrome 3		HP:0000341	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0004322	PMID:19206169	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001250	PMID:19206169	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001054	PMID:19206169;PMID:19416762	PCS		2/2			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0002162	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0030939	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000914	PMID:19206169	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000958	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0011220	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000316	PMID:19206169;PMID:19416762	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001646	OMIM:613707	TAS					P	HPO:probinson[2013-06-02]
OMIM:613707	Leopard syndrome 3		HP:0006610	PMID:19416762	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000256	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000358	PMID:19416762	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001249	PMID:19206169	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0003623	PMID:19206169	PCS					C	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0002212	PMID:19206169;PMID:19416762	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0007429	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000494	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001003	PMID:19206169;PMID:19416762	PCS		2/2			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0002750	PMID:19416762	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000470	PMID:19206169	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0005280	PMID:19206169;PMID:19416762	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000407	PMID:19206169	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000407	PMID:19416762	PCS	HP:0003621	1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001636	PMID:19206169;PMID:19416762	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001319	PMID:19206169	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0002967	PMID:19416762	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000268	PMID:19206169	PCS		1/1			P	HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000465	PMID:19206169	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0001510	PMID:19416762	PCS		1/1			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000369	PMID:19206169;PMID:19416762	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000006	PMID:19206169	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:613707	Leopard syndrome 3		HP:0000962	PMID:19206169;PMID:19416762	PCS		2/2			P	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10];HPO:probinson[2024-12-03]
OMIM:613707	Leopard syndrome 3		HP:0001633	OMIM:613707	TAS					P	HPO:probinson[2013-06-02]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0003621	PMID:23844677;PMID:23777631	PCS		2/6			C	HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0003387	PMID:23844677	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0003431	PMID:23777631	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0003596	PMID:23777631	PCS		4/5			C	HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0002650	PMID:23844677	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0003376	PMID:23844677	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0001761	PMID:23844677;PMID:23777631	PCS		5/5			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0003693	PMID:23844677;PMID:23777631	PCS		6/6			P	HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0003474	PMID:23844677	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0001284	PMID:23844677;PMID:23777631	PCS		6/6			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0002460	PMID:23844677;PMID:23777631	PCS		6/6			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0008180	PMID:23844677	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0000007	PMID:23777631	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0002936	PMID:23777631	PCS		4/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26]
OMIM:615376	Charcot-Marie-Tooth disease, recessive intermediate C		HP:0001765	PMID:23777631	PCS		3/5			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-03-26]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000286	PMID:31327508	PCS		2/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001250	PMID:31327508	PCS		5/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0010490	PMID:31327508	PCS		5/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001629	PMID:31327508	PCS	HP:0003577	3/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000319	PMID:31327508	PCS		4/4			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000316	PMID:31327508	PCS		2/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000659	PMID:31327508	PCS		1/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0002714	PMID:31327508	PCS		5/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001643	PMID:31327508	PCS	HP:0003623	2/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0006610	PMID:31327508	PCS		3/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0005989	PMID:31327508	PCS		2/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001249	PMID:31327508	PCS		4/4			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001344	PMID:31327508	PCS		4/4			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001640	PMID:31327508	PCS		1/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001263	PMID:31327508	PCS		4/4			P	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0005484	PMID:31327508	PCS		3/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0005180	PMID:31327508	PCS		1/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000407	PMID:31327508	PCS		2/4			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001317	PMID:31327508	IEA					P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000426	PMID:31327508	PCS		5/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000568	PMID:31327508	PCS		3/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000348	PMID:31327508	PCS		4/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001631	PMID:31327508	PCS	HP:0003577	2/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0008689	PMID:31327508	PCS		2/2	MALE		P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000006	PMID:31327508	PCS					I	HPO:probinson[2020-07-11];HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000589	PMID:31327508	PCS		4/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0000369	PMID:31327508	PCS		3/5			P	HPO:probinson[2020-07-11]
OMIM:618652	Neurooculocardiogenitourinary syndrome		HP:0001655	PMID:31327508	PCS	HP:0003623	1/5			P	HPO:probinson[2020-07-11]
OMIM:617561	Cohen-Gibson syndrome		HP:0000286	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0003015	PMID:25787343	PCS		1/1			P	HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0003577	OMIM:617561	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001792	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001176	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0001371	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001250	PMID:25787343	PCS		1/1			P	HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0001290	OMIM:617561	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617561	Cohen-Gibson syndrome		HP:0000518	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000938	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000316	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0001548	PMID:25787343	PCS		1/1			P	HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000337	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0100807	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001643	OMIM:617561	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0006610	PMID:25787343	PCS		1/1			P	HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000311	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000256	PMID:25787343	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000278	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0001249	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000995	PMID:25787343	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0002311	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000098	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000494	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000431	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000750	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0002650	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0002673	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001288	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001382	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001263	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0011823	PMID:25787343	PCS		1/1			P	HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0005280	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0400004	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0011304	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0012385	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0001816	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000508	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0001537	PMID:25787343	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0001833	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0005616	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000400	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0002866	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000369	OMIM:617561	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617561	Cohen-Gibson syndrome		HP:0000006	PMID:25787343	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000028	PMID:25787343	PCS		1/1			P	HPO:probinson[2021-09-23]
OMIM:617561	Cohen-Gibson syndrome		HP:0000545	PMID:25787343	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-23]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001298	PMID:27666369	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0003477	PMID:27666369	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0003676	PMID:27666369	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0002510	PMID:27666369	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0003577	PMID:27666369	PCS		1/6			C	HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0002650	PMID:27666369	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001344	PMID:27666369	PCS		2/6			P	HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0002079	PMID:27666369	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001272	PMID:27666369	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0003693	PMID:27666369	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001250	PMID:27666369	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001260	PMID:27666369	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001263	PMID:27666369	PCS	HP:0003593	6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001251	PMID:27666369	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0003593	PMID:27666369	PCS		4/6			C	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001290	PMID:27666369	PCS		4/6			P	HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001507	PMID:27666369	PCS		0/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30];HPO:probinson[2024-03-15]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0011463	PMID:27666369	PCS		1/6			C	HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0009027	PMID:27666369	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0000007	PMID:27666369	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0000648	PMID:27666369	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0007269	PMID:27666369	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001257	PMID:27666369	PCS		6/6			P	HPO:probinson[2020-12-30]
OMIM:617207	Encephalopathy, progressive, with amyotrophy and optic atrophy		HP:0001249	PMID:27666369	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-30]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0001561	OMIM:265300	IEA					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0002202	OMIM:265300	TAS					P	HPO:probinson[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0000431	OMIM:265300	TAS					P	HPO:probinson[2012-05-01]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0001530	OMIM:265300	IEA					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0001541	OMIM:265300	TAS					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0000282	OMIM:265300	IEA					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0030674	PMID:10946350	PCS		3/3			C	HPO:probinson[2024-03-09]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0000272	OMIM:265300	IEA					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0001790	PMID:10946350	PCS	HP:0030674	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0010741	OMIM:265300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0010310	PMID:10946350	PCS		3/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0005280	OMIM:265300	TAS					P	HPO:probinson[2012-05-01]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0012368	OMIM:265300	TAS					P	HPO:skoehler[2013-10-22]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0100540	OMIM:265300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0000969	OMIM:265300	TAS					P	HPO:probinson[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0000316	OMIM:265300	IEA					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0000767	OMIM:265300	IEA					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0000007	OMIM:265300	IEA					I	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0012281	PMID:10946350	PCS					P	HPO:skoehler[2013-04-18];HPO:probinson[2024-03-09]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0006521	PMID:10946350	PCS	HP:0003577	3/3			P	HPO:iea[2013-08-11];HPO:probinson[2024-03-09]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0002205	OMIM:265300	IEA					P	HPO:iea[2009-02-17]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0006533	PMID:10946350	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0001004	PMID:10946350	PCS		3/3			P	HPO:probinson[2024-03-09]
OMIM:265300	Lymphangiectasia, pulmonary, congenital		HP:0001249	PMID:10946350	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:607014	Hurler syndrome		HP:0002344	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0007957	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0007759	OMIM:607014	TAS					P	HPO:skoehler[2014-02-06]
OMIM:607014	Hurler syndrome		HP:0000365	OMIM:607014	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0003311	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0004322	OMIM:607014	TAS	HP:0011463				P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0001371	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:6000910	PMID:818611	PCS		10/10			P	HPO:probinson[2024-08-03]
OMIM:607014	Hurler syndrome		HP:0002180	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0000280	PMID:22557905	PCS	HP:0003593	1/1			P	HPO:probinson[2012-08-04];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0030812	OMIM:607014	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607014	Hurler syndrome		HP:0012471	PMID:22557905	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000316	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000238	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0000158	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0001488	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0001007	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0001249	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0004437	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0002673	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0001387	PMID:22557905	PCS		1/1			P	HPO:probinson[2012-08-04];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000293	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0003320	PMID:8468655	PCS		11/30			P	HPO:probinson[2012-08-04];HPO:probinson[2024-08-03]
OMIM:607014	Hurler syndrome		HP:0001263	OMIM:607014	TAS	HP:0011463				P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0000691	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0011400	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0004490	PMID:22557905	PCS	HP:0011463	1/1			P	HPO:probinson[2012-08-04];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0012185	OMIM:607014	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607014	Hurler syndrome		HP:0002869	OMIM:607014	TAS	HP:0011463				P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0001537	PMID:22557905	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000007	OMIM:607014	TAS					I	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0000403	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0001538	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0001659	OMIM:607014	TAS		4/12			P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0001653	OMIM:607014	TAS		10/12			P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0008802	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0005019	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0003016	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000463	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0004586	OMIM:607014	TAS	HP:0011463				P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0000023	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0002240	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0002680	OMIM:607014	TAS	HP:0011463				P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0100790	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0001706	OMIM:607014	TAS		11/58			P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0000455	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0000212	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0000894	OMIM:607014	TAS	HP:0011463				P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0000256	PMID:22557905	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0001744	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0002159	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0003541	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0000431	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000470	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0005280	OMIM:607014	TAS					P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0002808	OMIM:607014	TAS	HP:0011463				P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0008301	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000943	PMID:22557905	PCS		1/1			P	HPO:probinson[2012-08-04];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000546	OMIM:607014	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0001638	OMIM:607014	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607014	Hurler syndrome		HP:0002007	PMID:22557905	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0002205	OMIM:607014	TAS		4/12			P	HPO:probinson[2012-08-04]
OMIM:607014	Hurler syndrome		HP:0001433	PMID:22557905	PCS		1/1			P	HPO:probinson[2012-08-04];HPO:probinson[2022-03-27]
OMIM:607014	Hurler syndrome		HP:0000501	OMIM:607014	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:609039	Narcolepsy 3		HP:0002494	OMIM:609039	IEA					P	HPO:iea[2009-02-17]
OMIM:609039	Narcolepsy 3		HP:0002519	OMIM:609039	IEA					P	HPO:iea[2009-02-17]
OMIM:609039	Narcolepsy 3		HP:0001262	OMIM:609039	IEA					P	HPO:iea[2009-02-17]
OMIM:609039	Narcolepsy 3		HP:0002524	OMIM:609039	IEA					P	HPO:iea[2009-02-17]
OMIM:609039	Narcolepsy 3		HP:0030050	OMIM:609039	TAS					P	HPO:skoehler[2015-01-21]
OMIM:609039	Narcolepsy 3		HP:0000006	OMIM:609039	IEA					I	HPO:iea[2009-02-17]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000164	PMID:18834968	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000463	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002164	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0003196	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002680	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0003393	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0012368	PMID:18834968	PCS		1/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0003090	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000518	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0009540	PMID:18834968	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000938	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0011461	PMID:18834968	PCS		2/2			C	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0025019	PMID:18834968	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000978	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0008897	PMID:18834968	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002119	PMID:18834968	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002714	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002756	PMID:18834968	PCS		1/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0003645	PMID:18834968	PCS		0/1			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002650	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002132	PMID:18834968	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0001263	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000272	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0010557	PMID:18834968	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0009471	PMID:18834968	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0006184	PMID:18834968	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0009110	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000407	PMID:18834968	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000926	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0032199	PMID:18834968	PCS		0/1			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000007	PMID:18834968	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000307	PMID:18834968	PCS		1/2			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002208	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0001511	PMID:18834968	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0004944	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0002987	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000586	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0001873	PMID:18834968	PCS		0/1			P	HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000369	PMID:18834968	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0000545	PMID:18834968	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-08-28]
OMIM:612394	Bone fragility with contractures, arterial rupture, and deafness		HP:0001776	PMID:18834968	PCS		1/1			P	HPO:probinson[2022-08-28]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000286	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0003455	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000431	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000463	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0001250	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0010696	OMIM:202370	TAS	HP:0003623				P	HPO:probinson[2013-03-30]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0011220	OMIM:202370	IEA					P	HPO:skoehler[2019-02-22]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0001999	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000007	PMID:7719337	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-07]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0002705	OMIM:202370	TAS					P	HPO:skoehler[2017-07-13]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000348	OMIM:202370	IEA					P	HPO:skoehler[2019-02-22]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000846	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000218	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000268	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000565	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0002007	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0000369	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:202370	Peroxisome biogenesis disorder 2B		HP:0001249	OMIM:202370	IEA					P	HPO:iea[2009-02-17]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000343	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000062	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000260	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001250	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001252	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001274	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001290	OMIM:300215	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0011341	OMIM:300215	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001328	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0008872	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000219	OMIM:300215	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0002119	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000218	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001302	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0008734	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0009921	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001347	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0002014	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000054	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000431	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0002171	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0012736	OMIM:300215	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0011344	OMIM:300215	TAS					P	HPO:skoehler[2013-05-31]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000426	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001339	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000348	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001417	OMIM:300215	IEA					I	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0001257	OMIM:300215	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000347	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:300215	Lissencephaly, X-linked, 2		HP:0000369	OMIM:300215	IEA					P	HPO:skoehler[2010-06-19]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0000541	OMIM:600790	TAS					P	HPO:iea[2009-02-17]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0001135	OMIM:600790	TAS					P	HPO:iea[2009-02-17]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0001135	OMIM:600790	TAS	HP:0003577				P	HPO:iea[2015-07-20]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0000639	OMIM:600790	TAS					P	HPO:iea[2009-02-17]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0000505	OMIM:600790	TAS					P	HPO:iea[2009-02-17]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0000006	OMIM:600790	TAS					I	HPO:iea[2009-02-17]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0000545	OMIM:600790	TAS					P	HPO:iea[2009-02-17]
OMIM:600790	Chorioretinal atrophy, progressive bifocal		HP:0000533	OMIM:600790	TAS					P	HPO:iea[2015-07-19]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0003236	PMID:36264506	PCS		3/4			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0003596	PMID:36264506	PCS		1/4			C	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0000023	PMID:36344539	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0002094	PMID:36264506	PCS		4/4			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0001270	PMID:36264506	PCS		0/4			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0012444	PMID:36344539	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0033725	PMID:36344539	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0011463	PMID:36264506	PCS		2/4			C	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0001639	PMID:36264506	PCS		1/4			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0011462	PMID:36264506	PCS		1/4			C	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0009113	PMID:36264506	PCS		4/4			P	HPO:probinson[2023-07-10];HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0033364	PMID:36344539	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0000007	PMID:36264506	PCS					I	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0002878	PMID:36264506	PCS		2/4			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0001511	PMID:36344539	PCS		1/1			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0003306	PMID:36264506	PCS		3/4			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0002877	PMID:36264506	PCS		1/4			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0001249	PMID:36264506;PMID:36344539	PCS		1/5			P	HPO:probinson[2023-07-10]
OMIM:620326	Congenital myopathy 21 with early respiratory failure		HP:0003458	PMID:36264506	PCS		3/3			P	HPO:probinson[2023-07-10]
OMIM:607941	Atrial septal defect 2		HP:0003577	PMID:12845333	PCS		24/24			C	HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0001651	PMID:12845333	PCS		1/24			P	HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0001629	PMID:12845333	PCS		3/24			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0006695	PMID:12845333	PCS		1/24			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0001659	PMID:12845333	PCS		1/24			P	HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0001643	PMID:12845333	PCS		1/24			P	HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0001631	PMID:12845333	PCS		23/24			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0001653	PMID:12845333	PCS		1/24			P	HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0001642	PMID:12845333	PCS		6/24			P	HPO:probinson[2022-09-08]
OMIM:607941	Atrial septal defect 2		HP:0000006	PMID:12845333	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-08]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0003621	PMID:10625078	PCS		2/4			C	HPO:probinson[2022-04-30]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0032639	PMID:10625078	PCS		4/4			P	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0011462	PMID:10625078	PCS		2/4			C	HPO:probinson[2022-04-30]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0000613	PMID:10625078	PCS		3/4		HP:0012825	P	HPO:skoehler[2010-06-20];HPO:probinson[2022-04-30]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0000007	PMID:10625078	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-04-30]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0000531	PMID:10625078	PCS		4/4			P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-30]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0000479	PMID:10625078	PCS		0/4			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-04-30]
OMIM:219750	Cystinosis, adult nonnephropathic		HP:0003259	PMID:10625078	PCS		0/4			P	HPO:probinson[2022-04-30]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000582	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0003577	PMID:25754594	PCS		3/3			C	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0002188	PMID:19405097	PCS		1/1			P	HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0002023	PMID:25754594	PCS		1/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000089	OMIM:614083	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000122	PMID:25754594	PCS		2/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0003593	PMID:19405097	PCS		1/1			C	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000957	PMID:19405097	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0001903	OMIM:614083	TAS					P	HPO:probinson[2013-08-10]
OMIM:614083	Fanconi anemia, complementation group L		HP:0008551	PMID:25754594	PCS		1/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0040012	PMID:25754594	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000316	PMID:25754594	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000437	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000238	PMID:25754594	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0005528	OMIM:614083	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614083	Fanconi anemia, complementation group L		HP:0002575	PMID:25754594	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000054	PMID:25754594	PCS		1/1			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000175	PMID:25754594	PCS		1/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000431	OMIM:614083	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614083	Fanconi anemia, complementation group L		HP:0001321	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0011968	PMID:19405097	PCS		1/1			P	HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0002032	PMID:25754594	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0003221	PMID:19405097	PCS		1/1			P	HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0001263	OMIM:614083	TAS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000470	OMIM:614083	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000151	PMID:25754594	PCS		1/2			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0004590	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0009892	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000568	OMIM:614083	TAS		HP:0040283			P	HPO:skoehler[2015-10-05]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000007	PMID:19405097	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0009777	PMID:25754594	PCS		3/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0001511	PMID:25754594	PCS		2/3			P	HPO:skoehler[2015-10-05];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0001510	PMID:19405097	PCS		1/1			P	HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0007018	PMID:19405097	PCS		1/1			P	HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000465	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0003974	PMID:25754594	PCS		3/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000347	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0000369	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:614083	Fanconi anemia, complementation group L		HP:0001776	PMID:25754594	PCS		1/3			P	HPO:probinson[2022-09-24]
OMIM:604290	ACERULOPLASMINEMIA		HP:0000473	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0002168	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0001260	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0002396	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0003581	OMIM:604290	TAS					C	HPO:probinson[2012-07-16]
OMIM:604290	ACERULOPLASMINEMIA		HP:0025498	OMIM:604290	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604290	ACERULOPLASMINEMIA		HP:0001251	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0002072	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0002071	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0003281	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0000819	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0040303	OMIM:604290	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604290	ACERULOPLASMINEMIA		HP:0000726	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0001903	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0000007	OMIM:604290	IEA					I	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0000546	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:604290	ACERULOPLASMINEMIA		HP:0000643	OMIM:604290	IEA					P	HPO:iea[2009-02-17]
OMIM:614097	Acatalasemia		HP:0000155	OMIM:614097	TAS					P	HPO:probinson[2013-12-08]
OMIM:614097	Acatalasemia		HP:0000007	PMID:11001624	PCS					I	HPO:probinson[2013-12-08];HPO:probinson[2020-07-22]
OMIM:614097	Acatalasemia		HP:0012517	PMID:11001624	PCS					P	HPO:probinson[2014-01-08];HPO:probinson[2020-07-22]
OMIM:616858	Cowden syndrome 7		HP:0002895	PMID:26522472	PCS		6/7			P	HPO:probinson[2017-06-21]
OMIM:616858	Cowden syndrome 7		HP:0003002	OMIM:616858	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616858	Cowden syndrome 7		HP:0012740	OMIM:616858	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616858	Cowden syndrome 7		HP:0200008	OMIM:616858	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616858	Cowden syndrome 7		HP:0012844	PMID:26522472	PCS					P	HPO:probinson[2017-06-21]
OMIM:616858	Cowden syndrome 7		HP:0030075	OMIM:616858	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616858	Cowden syndrome 7		HP:0000256	PMID:26522472	PCS					P	HPO:probinson[2017-06-21]
OMIM:616858	Cowden syndrome 7		HP:0000872	OMIM:616858	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616858	Cowden syndrome 7		HP:0000006	PMID:26522472	PCS					I	HPO:probinson[2017-06-21]
OMIM:616858	Cowden syndrome 7		HP:0000853	OMIM:616858	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616858	Cowden syndrome 7		HP:0001028	PMID:26522472	PCS					P	HPO:probinson[2017-06-21]
OMIM:620332	Oocyte/zygote/embryo maturation arrest 18		HP:0008222	PMID:30877238	PCS		5/5			P	HPO:probinson[2023-07-09]
OMIM:620332	Oocyte/zygote/embryo maturation arrest 18		HP:0011462	PMID:30877238	PCS		5/5			C	HPO:probinson[2023-07-09]
OMIM:620332	Oocyte/zygote/embryo maturation arrest 18		HP:0000007	PMID:30877238	PCS					I	HPO:probinson[2023-07-09]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0000483	PMID:24482476	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0002464	PMID:24482476	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0000540	PMID:24482476	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001310	PMID:24482476	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001272	PMID:24482476	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001252	PMID:24482476	PCS	HP:0003623	3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0002064	PMID:24482476	PCS		2/2			P	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0100543	OMIM:616680	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0000639	PMID:24482476	PCS		5/5			P	HPO:probinson[2022-10-06];HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0011463	PMID:24482476	PCS		2/2			C	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0007663	PMID:24482476	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0002119	OMIM:616680	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0002313	PMID:24482476	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001347	PMID:24482476	PCS		2/2			P	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0003623	PMID:24482476	PCS		3/3			C	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0003487	PMID:24482476	PCS		5/5			P	HPO:probinson[2022-10-06];HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001260	PMID:24482476	PCS		0/2			P	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001263	PMID:24482476	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0007371	PMID:24482476	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0009830	PMID:24482476	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0000007	PMID:24482476	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0007256	PMID:24482476	PCS		3/3			P	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0000648	PMID:24482476	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001319	PMID:24482476	PCS	HP:0003623	3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0002505	PMID:24482476	PCS	HP:0011462	2/3			P	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0001257	PMID:24482476	PCS		5/5			P	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0006886	PMID:24482476	PCS		3/3			P	HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0003677	PMID:24482476	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0000501	PMID:24482476	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0002522	PMID:24482476	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0002600	PMID:24482476	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-06]
OMIM:616680	Spastic paraplegia 75, autosomal recessive		HP:0008944	PMID:24482476	PCS		3/3			P	HPO:probinson[2022-10-06]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0008936	PMID:32197075	PCS		6/6			P	HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0002059	PMID:32197075	PCS					P	HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0002188	PMID:32197075	PCS		5/6			P	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0002079	PMID:32197075	PCS		3/6			P	HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0001250	PMID:32197075	PCS	HP:0003593	6/6			P	HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0001263	PMID:32197075	PCS		6/6			P	HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0000007	PMID:32197075	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0006970	PMID:32197075	PCS					P	HPO:probinson[2020-06-27]
OMIM:618875	Seizures, early-onset, with neurodegeneration and brain calcification		HP:0012389	PMID:32197075	PCS		5/5			P	HPO:probinson[2020-06-27]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001396	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0003577	PMID:34711829	PCS		2/2			C	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001399	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0000122	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0003155	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001395	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001252	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0002240	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0011954	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001270	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001629	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001987	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001943	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0000774	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0002613	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0003026	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0031956	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0011649	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0005543	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0003124	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0006380	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0012021	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0000007	PMID:34711829	PCS					I	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001976	PMID:34711829	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0000126	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620454	Congenital disorder of glycosylation, type IIaa		HP:0001776	PMID:34711829	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0000164	PMID:24714551	PCS		0/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0003577	PMID:24714551	PCS		4/4			C	HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0002299	PMID:24714551	PCS		4/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0001596	OMIM:614929	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0045075	PMID:24714551	PCS		4/4			P	HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0008391	PMID:24714551	PCS		4/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0001806	PMID:24714551	PCS		4/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0002209	PMID:24714551	PCS		4/4			P	HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0000007	PMID:24714551	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0000653	PMID:24714551	PCS		4/4			P	HPO:skoehler[2013-04-18];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0000971	PMID:24714551	PCS		0/4			P	HPO:skoehler[2013-06-10];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0001810	PMID:24714551	PCS		4/4			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-05-08]
OMIM:614929	Ectodermal dysplasia 7, Hair/nail type		HP:0000951	PMID:24714551	PCS		0/4			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-05-08]
OMIM:600974	Deafness, neurosensory, autosomal recessive 7		HP:0003621	PMID:11850618	PCS		18/31			C	HPO:probinson[2022-03-31];HPO:probinson[2022-03-31]
OMIM:600974	Deafness, neurosensory, autosomal recessive 7		HP:0003577	PMID:11850618	PCS		13/31			C	HPO:probinson[2022-03-31]
OMIM:600974	Deafness, neurosensory, autosomal recessive 7		HP:0001751	PMID:11850618	PCS		0/31			P	HP:probinson[2019-05-10];HPO:probinson[2022-03-31]
OMIM:600974	Deafness, neurosensory, autosomal recessive 7		HP:0000407	PMID:11850618	PCS					P	HPO:probinson[2012-07-17];HP:probinson[2019-05-10]
OMIM:600974	Deafness, neurosensory, autosomal recessive 7		HP:0000007	PMID:11850618	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-05-10]
OMIM:611879	Cardiomyopathy, dilated, 1Z		HP:0003596	PMID:15542288	PCS		2/8			C	HPO:probinson[2022-07-03]
OMIM:611879	Cardiomyopathy, dilated, 1Z		HP:0003584	PMID:15542288	PCS		1/8			C	HPO:probinson[2022-07-03]
OMIM:611879	Cardiomyopathy, dilated, 1Z		HP:0011462	PMID:15542288	PCS		5/8			C	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:611879	Cardiomyopathy, dilated, 1Z		HP:0001635	PMID:15542288	PCS		6/7			P	HPO:probinson[2022-07-03]
OMIM:611879	Cardiomyopathy, dilated, 1Z		HP:0000006	PMID:15542288	TAS					I	HPO:probinson[2013-04-03]
OMIM:611879	Cardiomyopathy, dilated, 1Z		HP:0001645	PMID:15542288	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:611879	Cardiomyopathy, dilated, 1Z		HP:0001644	PMID:15542288	TAS		7/8			P	HPO:probinson[2013-01-09];HPO:probinson[2022-07-03]
OMIM:247610	Lymphoid interstitial pneumonia		HP:0001650	OMIM:247610	IEA					P	HPO:iea[2009-02-17]
OMIM:247610	Lymphoid interstitial pneumonia		HP:0006527	OMIM:247610	IEA					P	HPO:iea[2009-02-17]
OMIM:247610	Lymphoid interstitial pneumonia		HP:0000007	OMIM:247610	IEA					I	HPO:iea[2009-02-17]
OMIM:247610	Lymphoid interstitial pneumonia		HP:0001217	OMIM:247610	IEA					P	HPO:iea[2009-02-17]
OMIM:247610	Lymphoid interstitial pneumonia		HP:0001648	OMIM:247610	IEA					P	HPO:iea[2009-02-17]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0001265	OMIM:162400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0003202	PMID:23454272	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0002378	PMID:23454272	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0003387	OMIM:162400	IEA					P	HPO:iea[2009-02-17]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0003431	PMID:23454272	PCS		1/1			P	HPO:probinson[2021-11-24];HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0006858	PMID:23454272	IEA		1/1			P	HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0001761	PMID:23454272	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0006937	PMID:23454272	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0001284	OMIM:162400	TAS					P	HPO:skoehler[2010-06-20];HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0002460	PMID:23454272	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0000518	PMID:23454272	PCS	HP:0003621	1/1			P	HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0000407	OMIM:162400	IEA					P	HPO:iea[2009-02-17]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0006121	OMIM:162400	TAS					P	HPO:probinson[2022-01-29]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0002936	OMIM:162400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0007267	OMIM:162400	IEA					P	HPO:iea[2009-02-17]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0003409	OMIM:162400	TAS					P	HPO:probinson[2021-11-24];HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0001308	PMID:23454272	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0001868	OMIM:162400	IEA					P	HPO:iea[2009-02-17]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0003448	OMIM:162400	IEA					P	HPO:iea[2009-02-17]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0002359	PMID:23454272	PCS		1/1			P	HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0000006	PMID:11242114	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-11-24]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0001886	OMIM:162400	IEA					P	HPO:iea[2009-02-17]
OMIM:162400	Neuropathy, hereditary sensory and autonomic, type IA		HP:0002754	OMIM:162400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613908	Spinocerebellar ataxia 35		HP:0002311	PMID:21106500	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0000473	PMID:21106500	PCS		4/11			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0003596	PMID:21106500	PCS		11/11			C	HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0001288	PMID:21106500	PCS		8/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0003487	PMID:21106500	PCS		5/11			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0001310	PMID:21106500	PCS		11/11			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0001272	PMID:21106500	PCS		4/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0001260	PMID:21106500	PCS		10/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0001251	PMID:21106500	PCS		11/11			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0002080	PMID:21106500	PCS		4/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0010831	PMID:21106500	PCS		3/11			P	HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0000514	PMID:21106500	PCS		2/11			P	HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0007024	PMID:21106500	PCS		11/11			P	HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0002505	PMID:21106500	PCS		8/11			P	HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0000006	PMID:21106500	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0003677	PMID:21106500	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0000467	PMID:21106500	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:613908	Spinocerebellar ataxia 35		HP:0001347	PMID:21106500	PCS		10/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-01]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0025420	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0002240	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0100592	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0100651	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0034063	PMID:34183838	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0034062	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0011463	PMID:34183838	PCS		1/1			C	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0002958	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0002716	PMID:34183838	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0002878	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0020102	PMID:34183838	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0005528	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0200043	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0001744	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0001369	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0410243	PMID:34183838	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0025179	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0410241	PMID:34183838	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0003261	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:6000901	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0032271	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0000821	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0000403	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0000007	PMID:34183838	PCS					I	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0003237	PMID:34183838	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:621004	Autoimmune disease with susceptibility to mycobacterium tuberculosis		HP:0025329	PMID:34183838	PCS		0/1			P	ORCID:0000-0002-0736-9199[2025-02-03]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001650	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000286	PMID:26583190	PCS					P	HPO:probinson[2018-01-25]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000343	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000463	OMIM:243310	TAS					P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0004322	PMID:3351890	PCS					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000243	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001250	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001274	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0002162	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001252	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0003196	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001290	OMIM:243310	TAS					P	HPO:skoehler[2017-07-13]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001508	OMIM:243310	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001647	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000316	PMID:3351890	PCS					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000612	PMID:3351890	PCS					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000637	OMIM:243310	TAS					P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0008897	OMIM:243310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000219	OMIM:243310	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0002119	OMIM:243310	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001302	OMIM:243310	IEA					P	HPO:skoehler[2010-06-20]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001643	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000278	OMIM:243310	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001249	PMID:3351890	PCS					P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0002553	OMIM:243310	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000396	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000154	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000252	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000054	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000431	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001263	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000470	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0011800	OMIM:243310	IEA					P	HPO:skoehler[2018-10-08]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0010066	OMIM:243310	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000407	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000508	PMID:3351890	PCS					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0001339	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000568	OMIM:243310	TAS		HP:0040283			P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000307	OMIM:243310	TAS					P	HPO:skoehler[2015-09-11]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000202	OMIM:243310	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000006	OMIM:243310	TAS					I	HPO:skoehler[2012-10-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000567	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000028	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000369	OMIM:243310	IEA					P	HPO:iea[2009-02-17]
OMIM:243310	Baraitser-Winter syndrome 1		HP:0000204	OMIM:243310	IEA		HP:0040283			P	HPO:probinson[2017-05-29]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000486	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000023	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000276	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000490	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000272	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0011800	OMIM:609944	TAS					P	HPO:skoehler[2013-11-28]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0045075	OMIM:609944	TAS					P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0045074	OMIM:609944	TAS					P	HPO:probinson[2022-05-08]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000407	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000968	OMIM:609944	TAS					P	HPO:probinson[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0002808	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0001939	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000426	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000613	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000767	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000007	OMIM:609944	IEA					I	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0009466	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000218	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0030084	OMIM:609944	TAS					P	HPO:skoehler[2015-12-30]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000047	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000322	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000347	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0001128	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:609944	Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features		HP:0000621	OMIM:609944	IEA					P	HPO:iea[2009-02-17]
OMIM:618849	Bone marrow failure syndrome 6		HP:0030413	PMID:32300648	PCS		1/4			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0011904	PMID:32300648	PCS		2/4			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0031413	PMID:32300648	PCS					P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0011108	PMID:32300648	PCS		1/4			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0012432	PMID:32300648	PCS		2/4			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0001903	PMID:32300648	PCS					P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0000938	PMID:32300648	PCS		1/4			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0001888	PMID:32300648	PCS					P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0000821	PMID:32300648	PCS		1/4			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0005518	PMID:32300648	PCS		2/4			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0005528	PMID:32300648	PCS		3/3			P	HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0000006	PMID:32300648	PCS					I	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0001875	PMID:32300648	PCS					P	HPO:probinson[2020-06-20];HPO:probinson[2020-06-20]
OMIM:618849	Bone marrow failure syndrome 6		HP:0003326	PMID:32300648	PCS		2/4			P	HPO:probinson[2020-06-20]
OMIM:251700	Microphthalmia with hyperopia, retinal degeneration, macrophakia,and dental anomalies		HP:0000164	OMIM:251700	IEA					P	HPO:iea[2009-02-17]
OMIM:251700	Microphthalmia with hyperopia, retinal degeneration, macrophakia,and dental anomalies		HP:0008499	OMIM:251700	IEA					P	HPO:iea[2009-02-17]
OMIM:251700	Microphthalmia with hyperopia, retinal degeneration, macrophakia,and dental anomalies		HP:0000007	OMIM:251700	IEA					I	HPO:iea[2009-02-17]
OMIM:251700	Microphthalmia with hyperopia, retinal degeneration, macrophakia,and dental anomalies		HP:0000546	OMIM:251700	IEA					P	HPO:iea[2009-02-17]
OMIM:251700	Microphthalmia with hyperopia, retinal degeneration, macrophakia,and dental anomalies		HP:0000568	OMIM:251700	IEA					P	HPO:iea[2009-02-17]
OMIM:251700	Microphthalmia with hyperopia, retinal degeneration, macrophakia,and dental anomalies		HP:0000501	OMIM:251700	IEA					P	HPO:iea[2009-02-17]
OMIM:605818	Deafness, autosomal recessive 27		HP:0000407	OMIM:605818	TAS					P	HPO:skoehler[2015-09-11]
OMIM:605818	Deafness, autosomal recessive 27		HP:0000007	OMIM:605818	TAS					I	HPO:skoehler[2015-09-11]
OMIM:614915	Lethal congenital contracture syndrome 4		HP:0003202	OMIM:614915	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614915	Lethal congenital contracture syndrome 4		HP:0003577	PMID:22610851	PCS		4/4			C	HPO:probinson[2022-10-10]
OMIM:614915	Lethal congenital contracture syndrome 4		HP:0001371	OMIM:614915	IEA					P	HPO:skoehler[2013-01-11]
OMIM:614915	Lethal congenital contracture syndrome 4		HP:0005684	OMIM:614915	IEA					P	HPO:skoehler[2013-01-09]
OMIM:614915	Lethal congenital contracture syndrome 4		HP:0002828	OMIM:614915	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614915	Lethal congenital contracture syndrome 4		HP:0000007	PMID:22610851	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-10]
OMIM:614915	Lethal congenital contracture syndrome 4		HP:0002093	OMIM:614915	IEA					P	HPO:skoehler[2019-09-07]
OMIM:255200	Myopathy, centronuclear, 2		HP:0010628	PMID:17676042	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003577	PMID:17676042	PCS		4/5			C	HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001371	PMID:17676042	PCS	HP:0003577	3/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003691	OMIM:255200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0002460	OMIM:255200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001270	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003391	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0008872	OMIM:255200	IEA					P	HPO:iea[2009-02-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003307	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0002515	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0000218	OMIM:255200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003327	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003701	PMID:17676042	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003700	OMIM:255200	IEA					P	HPO:iea[2009-02-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001562	PMID:17676042	PCS		3/5			P	HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003687	PMID:17676042	PCS		4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003621	PMID:17676042	PCS		1/5			C	HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0002650	OMIM:255200	IEA					P	HPO:iea[2009-02-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001762	OMIM:255200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0000276	OMIM:255200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001761	OMIM:255200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001260	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001284	OMIM:255200	IEA					P	HPO:iea[2009-02-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001618	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0002808	OMIM:255200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0000508	OMIM:255200	IEA					P	HPO:iea[2009-02-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0000602	PMID:17676042	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0000007	PMID:17676042	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001558	PMID:17676042	PCS		3/5			P	HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001319	OMIM:255200	IEA					P	HPO:iea[2009-02-17]
OMIM:255200	Myopathy, centronuclear, 2		HP:0002747	PMID:17676042	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0001511	PMID:17676042	PCS		3/5			P	HPO:probinson[2022-08-18]
OMIM:255200	Myopathy, centronuclear, 2		HP:0003458	OMIM:255200	IEA					P	HPO:iea[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003554	PMID:23332920;OMIM:160565	PCS		18/19			P	HPO:probinson[2023-03-07];HPO:skoehler[2014-11-26]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003236	PMID:23332920	PCS		11/11			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0000662	OMIM:160565	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003552	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003198	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0001371	OMIM:160565	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003394	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0011463	PMID:23332920	PCS		5/11			C	HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0009046	OMIM:160565	TAS					P	HPO:skoehler[2014-11-26]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0009005	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0000615	OMIM:160565	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003803	PMID:23332920	PCS		6/9			P	HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0007126	OMIM:160565	TAS					P	HPO:skoehler[2014-11-26]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003701	PMID:23332920	PCS		8/11			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0002359	OMIM:160565	TAS					P	HPO:skoehler[2014-11-26]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003621	PMID:23332920	PCS		2/11			C	HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003388	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003581	OMIM:160565	TAS		4/11			C	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0002093	OMIM:160565	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0034392	PMID:23332920	PCS		6/11			P	HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003738	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003677	OMIM:160565	TAS					C	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0000006	PMID:23332920	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0002522	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0003557	OMIM:160565	TAS		4/9			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-07]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0002600	OMIM:160565	TAS					P	HPO:probinson[2009-02-17]
OMIM:160565	Myopathy, tubular aggregate, 1		HP:0000544	PMID:23332920	PCS		2/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-07]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003158	PMID:32869508	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000121	PMID:16705067;PMID:26136118;PMID:32869508;PMID:16501001;PMID:26426912;PMID:24321194;PMID:18816383;PMID:25477417;PMID:10878661;PMID:27067446;PMID:21669885;PMID:25852890	PCS		59/59			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000483	PMID:32869508;PMID:18816383;PMID:10878661;PMID:27067446;PMID:25852890	PCS		2/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000486	PMID:32869508;PMID:18816383;PMID:10878661;PMID:27067446;PMID:25852890	PCS		1/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0004322	PMID:18816383;PMID:27067446;PMID:21669885	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0001250	OMIM:248250	IEA					P	HPO:iea[2009-02-17]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003155	PMID:27067446	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000083	PMID:16705067;PMID:32869508;PMID:16501001;PMID:26426912;PMID:24321194;PMID:25477417;PMID:27067446;PMID:21669885	PCS		32/32			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0004363	PMID:10878661	PCS		0/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003593	PMID:16705067;PMID:32869508;PMID:16501001;PMID:18816383;PMID:25477417;PMID:27067446;PMID:25852890	PCS		19/33			C	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0010049	PMID:26426912	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0012587	PMID:16705067;PMID:26426912;PMID:24321194;PMID:27067446	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0012622	OMIM:248250	TAS					P	HPO:probinson[2014-01-18]
OMIM:248250	Hypomagnesemia 3, renal		HP:0031425	PMID:27067446	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000639	PMID:32869508;PMID:18816383;PMID:27067446;PMID:25852890	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0011463	PMID:26426912;PMID:24321194;PMID:25477417;PMID:27067446	PCS		11/37			C	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0011462	PMID:26136118;PMID:26426912;PMID:24321194	PCS		5/12			C	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002979	PMID:16501001	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002857	PMID:27067446	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0001324	PMID:27067446	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003149	PMID:25477417	PCS		13/24			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000010	PMID:16501001;PMID:24321194;PMID:18816383;PMID:25477417;PMID:10878661;PMID:25852890	PCS		23/42			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002199	PMID:16705067;PMID:32869508;PMID:26426912;PMID:21669885	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003165	PMID:26136118;PMID:32869508;PMID:24321194;PMID:25477417;PMID:10878661;PMID:27067446;PMID:25852890	PCS		36/39			P	HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002150	PMID:16705067;PMID:26136118;PMID:32869508;PMID:16501001;PMID:26426912;PMID:24321194;PMID:18816383;PMID:25477417;PMID:10878661;PMID:27067446;PMID:21669885;PMID:25852890	PCS		54/58			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000093	PMID:25852890	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0100586	PMID:25477417	PCS		14/24			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002907	PMID:24321194;PMID:25477417	PCS		6/25			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002905	PMID:32869508;PMID:26426912;PMID:27067446	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002748	PMID:25477417	PCS		2/24			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000007	PMID:16705067;PMID:10390358	PCS		20/20			I	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002901	PMID:26136118;PMID:16501001;PMID:26426912;PMID:24321194;PMID:18816383;PMID:27067446;PMID:25852890	PCS		8/13			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002027	PMID:26136118;PMID:25477417	PCS		9/25			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002149	PMID:26136118;PMID:32869508;PMID:25852890	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003774	PMID:16705067;PMID:26136118;PMID:32869508;PMID:16501001;PMID:26426912;PMID:24321194;PMID:18816383;PMID:25477417;PMID:27067446;PMID:21669885;PMID:25852890	PCS		7/45			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000540	PMID:32869508;PMID:18816383;PMID:27067446;PMID:25852890	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0012608	PMID:16705067;PMID:32869508;PMID:16501001;PMID:24321194;PMID:18816383;PMID:25477417;PMID:10878661;PMID:27067446;PMID:21669885;PMID:25852890	PCS		43/45			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0012405	PMID:24321194;PMID:25477417;PMID:10878661	PCS		19/29			P	HPO:skoehler[2013-11-18];HPO:probinson[2024-03-08];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0012406	PMID:10878661	PCS		9/9			P	HPO:probinson[2022-11-24]
OMIM:248250	Hypomagnesemia 3, renal		HP:0033786	PMID:32869508;PMID:26426912	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0001508	OMIM:248250;PMID:18816383;PMID:25477417	PCS		18/35			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002917	PMID:16705067;PMID:26136118;PMID:32869508;PMID:16501001;PMID:26426912;PMID:24321194;PMID:18816383;PMID:10878661;PMID:27067446;PMID:21669885;PMID:25852890	PCS		33/34			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0012052	PMID:26426912	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0006297	PMID:32869508;PMID:26426912	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0008872	OMIM:248250	IEA					P	HPO:iea[2009-02-17]
OMIM:248250	Hypomagnesemia 3, renal		HP:0001941	PMID:32869508;PMID:16501001	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003621	PMID:16705067;PMID:26426912;PMID:24321194;PMID:18816383;PMID:25477417;PMID:21669885	PCS		11/40			C	HPO:iea[2009-02-17];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0005567	PMID:26136118;PMID:32869508;PMID:18816383;PMID:25477417;PMID:10878661;PMID:27067446;PMID:21669885	PCS		41/41			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0002013	PMID:25477417	PCS		8/24			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000790	OMIM:248250	IEA					P	HPO:iea[2009-02-17]
OMIM:248250	Hypomagnesemia 3, renal		HP:0012637	PMID:26136118;PMID:21669885	PCS		2/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0001281	PMID:25477417	PCS		3/24			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000705	PMID:32869508;PMID:26426912	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0008341	PMID:18816383;PMID:10878661	PCS		6/7			P	HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0001959	PMID:18816383;PMID:25477417;PMID:10878661;PMID:27067446;PMID:25852890	PCS		35/40			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000822	PMID:24321194;PMID:18816383	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000103	PMID:32869508;PMID:18816383;PMID:25477417;PMID:10878661;PMID:27067446;PMID:25852890	PCS		36/41			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0003259	PMID:16705067;PMID:32869508;PMID:24321194;PMID:27067446	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000545	PMID:32869508;PMID:18816383;PMID:27067446;PMID:25852890	PCS		1/5			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:248250	Hypomagnesemia 3, renal		HP:0000787	PMID:16705067;PMID:26136118;PMID:24321194;PMID:25477417	PCS		9/32			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-14];ORCID:0000-0002-0736-9199[2024-04-14]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0030234	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0008981	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0009046	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0000007	PMID:31610034	PCS					I	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0012548	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0002527	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0003701	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0003713	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618848	Muscular dystrophy, limb-girdle, autosomal recessive 26		HP:0003557	PMID:31610034	PCS					P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000286	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001770	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0003038	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000365	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0006507	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0003196	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000085	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0010806	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0010049	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001171	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000316	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0009623	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001841	OMIM:609945	TAS					P	HPO:probinson[2013-04-02]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001840	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000054	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000252	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0002750	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0004058	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001263	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0003083	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0006380	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0008362	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0010561	OMIM:609945	IEA					P	HPO:skoehler[2010-06-18]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0002827	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000767	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0002869	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000568	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000048	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000047	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0002866	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000006	OMIM:609945	IEA					I	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0002984	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0005613	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000384	OMIM:609945	TAS					P	HPO:skoehler[2013-04-18]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000023	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001156	OMIM:609945	TAS					P	HPO:skoehler[2014-11-26]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000581	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0003175	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000060	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0010743	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0009760	OMIM:609945	TAS					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0007385	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000218	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0008830	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000378	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000894	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0009803	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000396	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000473	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001363	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0002697	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000233	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000431	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001762	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001162	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0003022	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000470	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0003065	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0003182	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0005160	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0011304	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0010781	OMIM:609945	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000508	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001839	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0008386	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0009556	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001631	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0009756	OMIM:609945	TAS					P	HPO:iea[2012-06-03]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000028	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0000347	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0004987	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:609945	Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia		HP:0001831	OMIM:609945	IEA					P	HPO:iea[2009-02-17]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0002487	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0005216	PMID:36647078	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0007957	PMID:36647078	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0000189	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0001252	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0032794	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0003390	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0011476	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0100785	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0011385	PMID:36647078	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0000637	PMID:33439489;PMID:36647078	PCS		3/3			P	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0003623	PMID:33439489;PMID:36647078	PCS		3/3			C	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0005469	PMID:36647078	PCS		2/2			P	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0002553	PMID:33439489;PMID:36647078	PCS		3/3			P	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0001288	PMID:36647078	PCS		2/2			P	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0000298	PMID:36647078	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0011968	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0001263	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0001284	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0012736	PMID:36647078	PCS		2/2			P	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0034252	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0000729	PMID:36647078	PCS		2/2			P	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0000508	PMID:36647078	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0030890	PMID:36647078	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0000007	PMID:33439489	PCS					I	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0008586	PMID:36647078	PCS		1/2			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0100716	PMID:33439489	PCS		1/1			P	HPO:probinson[2024-03-10]
OMIM:620469	Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay		HP:0000324	PMID:36647078	PCS		2/2			P	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0011908	PMID:22431104	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0004322	PMID:22431104	PCS		1/1			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0000122	PMID:22431104	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0003022	PMID:22431104	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0010972	PMID:22431104	PCS		1/1			P	HPO:probinson[2017-12-22];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0009380	PMID:22431104	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0012139	PMID:22431104	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0100337	PMID:22431104	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0034197	PMID:22431104	PCS		1/1			C	HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0001647	PMID:22431104	PCS		1/1			P	HPO:skoehler[2013-01-09]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0009777	PMID:22431104	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0000625	PMID:22431104	PCS		1/1			P	HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0005528	PMID:22431104	PCS		1/1			P	HPO:probinson[2017-12-22];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0006368	PMID:22431104	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0000413	PMID:22431104	PCS		1/1			P	HPO:skoehler[2013-01-09]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0000006	PMID:22431104	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0002984	PMID:22431104	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0000402	PMID:22431104	PCS		1/1			P	HPO:skoehler[2013-01-09];HPO:probinson[2023-04-11]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0001875	PMID:22431104	PCS		1/1			P	HPO:skoehler[2015-08-16]
OMIM:614900	Diamond-Blackfan anemia 11		HP:0002974	PMID:22431104	PCS		1/1			P	HPO:skoehler[2018-10-08]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003431	PMID:12112076	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003376	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001178	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003693	OMIM:145900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001252	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0002460	OMIM:145900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003593	PMID:12112076	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001270	PMID:12112076	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001171	OMIM:145900	TAS					P	HPO:skoehler[2015-12-30]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0000639	OMIM:145900	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0009027	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0002936	OMIM:145900	TAS					P	HPO:skoehler[2013-03-27]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001308	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003448	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003701	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001763	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001765	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001265	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0002751	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0002136	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0002650	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001761	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003383	PMID:12112076	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0001284	PMID:12112076	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003382	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003481	PMID:12112076	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0003380	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0010871	PMID:12112076	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0011096	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0009053	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0030175	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0000007	PMID:12112076	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0002922	OMIM:145900	IEA					P	HPO:iea[2009-02-17]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0006886	PMID:12112076	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:145900	Hypertrophic neuropathy of dejerine-sottas		HP:0000006	OMIM:145900	IEA					I	HPO:iea[2009-02-17]
OMIM:160570	Myopathy with storage of glycoproteins and glycosaminoglycans		HP:0003236	OMIM:160570	TAS					P	HPO:iea[2009-02-17]
OMIM:160570	Myopathy with storage of glycoproteins and glycosaminoglycans		HP:0003198	OMIM:160570	TAS					P	HPO:skoehler[2009-02-17]
OMIM:160570	Myopathy with storage of glycoproteins and glycosaminoglycans		HP:0008970	OMIM:160570	IEA					P	HPO:skoehler[2010-06-20]
OMIM:160570	Myopathy with storage of glycoproteins and glycosaminoglycans		HP:0000006	OMIM:160570	IEA					I	HPO:iea[2009-02-17]
OMIM:300228	Testicular germ cell tumor 1		HP:0100728	OMIM:300228	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300228	Testicular germ cell tumor 1		HP:0001417	OMIM:300228	IEA					I	HPO:skoehler[2013-01-11]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0003577	PMID:21551322	IEA		1/5			C	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0003596	PMID:11273725;PMID:21551322	PCS		5/15			C	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0003584	PMID:21551322	PCS		1/5			C	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0005110	PMID:21551322	PCS		1/5			P	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0011664	PMID:21551322;PMID:29024827	PCS		9/10			P	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0033755	PMID:21551322	PCS		3/5			P	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0010316	PMID:29024827	IEA		2/5			P	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0011463	PMID:11273725	PCS		1/10			C	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0011462	PMID:11273725;PMID:21551322;PMID:29024827	PCS		8/20			C	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0011461	PMID:29024827	PCS		2/5			C	HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0001635	PMID:11273725;PMID:21551322	PCS		6/12			P	HPO:probinson[2022-07-04];HPO:probinson[2013-04-03];HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0001653	PMID:21551322	PCS		1/5			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0004756	PMID:11273725	PCS		1/6			P	HPO:probinson[2013-04-03];HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0000006	PMID:11273725	PCS					I	HPO:probinson[2013-04-03];HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0001644	PMID:11273725	PCS		5/8			P	HPO:probinson[2013-01-09];HPO:probinson[2022-07-04]
OMIM:611878	Cardiomyopathy, dilated, 1Y		HP:0003623	PMID:29024827	PCS		2/5			C	HPO:probinson[2022-07-04]
OMIM:108800	Atrial septal defect 1		HP:0001650	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0001682	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0001684	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0005301	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0001629	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0011706	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0001647	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0012516	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0001631	PMID:9610535	PCS					P	HPO:iea[2009-02-17]
OMIM:108800	Atrial septal defect 1		HP:0011995	PMID:9610535	PCS					P	HPO:lccarmody[2018-06-27]
OMIM:108800	Atrial septal defect 1		HP:0000006	OMIM:108800	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:600975	Glaucoma 3, primary infantile, B		HP:0000007	OMIM:600975	IEA					I	HPO:iea[2009-02-17]
OMIM:600975	Glaucoma 3, primary infantile, B		HP:0008007	OMIM:600975	IEA					P	HPO:iea[2009-02-17]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0001882	PMID:26712909	PCS					P	HPO:probinson[2017-06-20]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0002099	OMIM:616871	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0003581	OMIM:616871	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0031688	OMIM:616871	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0012311	PMID:25920683	PCS					P	HPO:probinson[2017-06-20]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0004808	PMID:25920683	PCS					P	HPO:probinson[2017-06-20]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0003829	OMIM:616871	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0000964	OMIM:616871	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0002725	OMIM:616871	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0005528	PMID:26712909	PCS					P	HPO:probinson[2017-06-20]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0005505	PMID:25920683	PCS					P	HPO:probinson[2017-06-20]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0000006	PMID:26712909	PCS					I	HPO:probinson[2017-06-20]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0002863	PMID:25920683	PCS					P	HPO:probinson[2017-06-20]
OMIM:616871	Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to		HP:0002665	OMIM:616871	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613909	Spinocerebellar ataxia 32		HP:0100543	OMIM:613909	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613909	Spinocerebellar ataxia 32		HP:0001272	OMIM:613909	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613909	Spinocerebellar ataxia 32		HP:0001251	OMIM:613909	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613909	Spinocerebellar ataxia 32		HP:0000789	OMIM:613909	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613909	Spinocerebellar ataxia 32		HP:0000029	OMIM:613909	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613909	Spinocerebellar ataxia 32		HP:0000006	OMIM:613909	TAS					I	HPO:skoehler[2017-07-13]
OMIM:613909	Spinocerebellar ataxia 32		HP:0000027	OMIM:613909	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0004322	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0001250	PMID:22241097	PCS		3/6			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0045075	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0011480	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0001508	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000957	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0011463	PMID:18183042	PCS		2/2			C	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0010296	PMID:22241097	PCS		1/6			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0006297	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000612	PMID:22241097	PCS		1/6		HP:0012833	P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000219	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000218	PMID:22241097	PCS		1/6			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000653	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000256	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0001348	PMID:22241097	PCS		1/6			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000456	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000252	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000750	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0001263	PMID:22241097;PMID:18183042	PCS		7/7			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000053	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000272	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0002293	PMID:18183042	PCS		2/2			P	HPO:probinson[2021-08-19];HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0001181	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0100336	PMID:22241097	PCS		1/7			P	HPO:probinson[2024-03-08]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0100337	PMID:22241097	PCS		1/7			P	HPO:probinson[2024-03-08]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000767	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000047	PMID:22241097	PCS		1/6	MALE		P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0000006	PMID:18183042	PCS					I	HPO:probinson[2021-08-19];HPO:probinson[2022-12-03]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0001634	PMID:22241097	PCS		1/7			P	HPO:probinson[2021-08-19]
OMIM:618874	Chromosome 17q11.2 duplication syndrome, 1.4-Mb		HP:0002126	PMID:22241097	PCS		1/6			P	HPO:probinson[2021-08-19]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0004325	OMIM:616681	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0001034	PMID:25259927	PCS		2/2			P	HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0003577	PMID:25259927	PCS		2/2			C	HPO:probinson[2023-02-25];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000340	PMID:25259927	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0002510	PMID:25259927	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0020073	PMID:25259927	PCS		2/2			P	HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0004322	OMIM:616681	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000194	PMID:25259927	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0001250	PMID:25259927	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0001274	PMID:25259927	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0001263	OMIM:616681	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0001181	PMID:25259927;OMIM:616681	PCS		11/12			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0006380	PMID:25259927	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000506	PMID:25259927	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0011451	PMID:25259927	PCS		2/2			P	HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000508	PMID:25259927	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000007	PMID:25259927	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0002307	PMID:25259927	PCS		1/1			P	HPO:probinson[2023-02-25];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0001257	PMID:25259927	PCS		2/2			P	HPO:probinson[2023-02-25];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000028	PMID:25259927	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000501	PMID:25259927	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0000347	PMID:25259927	PCS		1/2			P	HPO:skoehler[2015-12-30]
OMIM:616681	Microcephaly 16, primary, autosomal recessive		HP:0009879	PMID:25259927	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:620333	Oocyte/zygote/embryo maturation arrest 19		HP:0008222	PMID:30877238	PCS		3/3			P	HPO:probinson[2023-07-11]
OMIM:620333	Oocyte/zygote/embryo maturation arrest 19		HP:0011462	PMID:30877238	PCS		3/3			C	HPO:probinson[2023-07-11]
OMIM:620333	Oocyte/zygote/embryo maturation arrest 19		HP:0000007	PMID:30877238	PCS					I	HPO:probinson[2023-07-11]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0001264	PMID:24334290	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0000486	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0001288	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0002079	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0003487	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0002497	PMID:24334290	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0001250	PMID:24334290	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0002154	PMID:21471552	PCS		8/8			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-16]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0001260	PMID:24334290	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0002151	PMID:24334290	PCS		4/7			P	HPO:probinson[2017-06-18];HPO:probinson[2024-03-16]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0002490	PMID:24334290	PCS		2/7			P	HPO:probinson[2024-03-16]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:6000829	PMID:24334290	PCS		2/2			P	HPO:probinson[2024-08-03]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0500230	PMID:24334290	PCS		4/8			P	HPO:probinson[2024-03-16]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0000639	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0002928	PMID:24334290	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0000007	PMID:24334290	PCS					I	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0007256	PMID:24334290	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0000648	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0000505	OMIM:616859	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0002415	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0001257	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:616859	Spasticity, childhood-onset, with hyperglycinemia		HP:0001347	PMID:21471552	PCS					P	HPO:probinson[2017-06-18]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001133	OMIM:304700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0002015	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001332	PMID:10878669	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001260	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0000708	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0000408	OMIM:304700	PCS					P	HPO:probinson[2012-03-30]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0100704	OMIM:304700	PCS					P	HPO:probinson[2012-03-30]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0011463	PMID:10878669	PCS		1/1			C	HPO:probinson[2012-03-30];HPO:probinson[2022-12-14]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001419	PMID:8841189	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0008596	PMID:10878669;OMIM:304700	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14];HPO:probinson[2012-03-30]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0000613	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0007663	OMIM:304700	TAS					P	HPO:skoehler[2015-07-26]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0000505	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0002659	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0008954	PMID:10878669	PCS		1/1			P	HPO:probinson[2022-12-14]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001268	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001257	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0000512	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0002533	PMID:10878669	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0000545	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001337	OMIM:304700	IEA					P	HPO:iea[2009-02-17]
OMIM:304700	Mohr-Tranebjaerg syndrome		HP:0001347	PMID:10878669	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-14]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003577	PMID:21549344	PCS		1/2			C	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0002089	PMID:21549344	PCS		2/2		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0025401	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003593	PMID:21549344	PCS		1/2			C	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001270	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0012664	PMID:21549344	PCS		2/2			P	HPO:probinson[2022-10-23];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001508	PMID:21549344	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001522	PMID:21549344	PCS		1/2			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001942	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003688	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003128	PMID:21549344	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001265	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003324	PMID:21549344	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0002353	PMID:21549344	PCS		2/2			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001640	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0011968	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0002151	PMID:21549344	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0011923	PMID:21549344	PCS		2/2			P	HPO:probinson[2022-10-23];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003819	PMID:21549344	PCS		1/2			C	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001639	PMID:21549344	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0001635	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0000007	PMID:21549344	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0008347	PMID:21549344	PCS		2/2			P	HPO:probinson[2022-10-23];HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003811	PMID:21549344	PCS		1/2			C	HPO:probinson[2022-10-23]
OMIM:614096	Combined oxidative phosphorylation deficiency 8		HP:0003557	PMID:21549344	PCS		1/2			P	HPO:probinson[2022-10-23]
OMIM:133100	Erythrocytosis, familial, 1		HP:0001342	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0002641	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0002321	OMIM:133100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0001050	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0012378	OMIM:133100	TAS					P	HPO:skoehler[2013-10-22]
OMIM:133100	Erythrocytosis, familial, 1		HP:0000822	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0001658	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0001900	PMID:8093406	PCS		33/33			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:133100	Erythrocytosis, familial, 1		HP:0001899	PMID:8093406	PCS		33/33			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:133100	Erythrocytosis, familial, 1		HP:0002315	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0000006	PMID:8093406	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:133100	Erythrocytosis, familial, 1		HP:0001744	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:133100	Erythrocytosis, familial, 1		HP:0001898	PMID:8093406	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-30]
OMIM:133100	Erythrocytosis, familial, 1		HP:0002875	OMIM:133100	IEA					P	HPO:iea[2009-02-17]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0001596	PMID:17107387	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0002231	PMID:17107387	PCS		7/7			P	HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0000007	PMID:17107387	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0012746	PMID:17107387	PCS		7/7			P	HPO:skoehler[2014-04-04];HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0001598	PMID:17107387	PCS		7/7			P	HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0000971	PMID:17107387	PCS		0/7			P	HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0001810	PMID:17107387	PCS		7/7			P	HPO:skoehler[2012-11-16];HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0008070	PMID:17107387	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-06-25]
OMIM:614928	Ectodermal dysplasia 6, Hair/nail type		HP:0001249	PMID:17107387	PCS		0/7			P	HPO:probinson[2024-06-25]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002663	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002982	OMIM:600785	TAS					P	HPO:probinson[2012-05-01]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002752	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0003013	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002980	OMIM:600785	TAS					P	HPO:probinson[2012-05-01]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0001596	OMIM:600785	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002970	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0003025	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0003165	OMIM:600785	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0003155	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0003593	OMIM:600785	TAS					C	HPO:probinson[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0030839	OMIM:600785	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0010502	OMIM:600785	TAS					P	HPO:probinson[2012-05-01]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0031415	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0006462	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002748	OMIM:600785	TAS					P	HPO:probinson[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0006463	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0006487	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002857	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0003745	OMIM:600785	IEA					I	HPO:iea[2009-02-17]
OMIM:600785	Vitamin D-dependent rickets type 2B with normal vitamin D receptor		HP:0002753	OMIM:600785	IEA					P	HPO:iea[2009-02-17]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000286	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002069	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000365	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0004322	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001250	PMID:36528028	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0004442	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:5200310	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000160	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001252	PMID:36528028	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000041	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0003593	PMID:36528028	PCS		15/15			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0032794	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0004482	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002180	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0033725	PMID:36528028	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0012469	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0012110	PMID:36528028	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0011342	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000717	PMID:36528028	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000637	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0040019	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001643	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002019	PMID:36528028	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001007	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001249	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000252	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001344	PMID:36528028	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0011968	PMID:36528028	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002791	PMID:36528028	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002033	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001263	PMID:36528028	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002194	PMID:36528028	PCS		13/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0033454	PMID:36528028	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0011097	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0007270	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000609	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000007	PMID:36528028	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001257	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0007359	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000322	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000006	PMID:36528028	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001276	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000582	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000463	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002121	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0010862	PMID:36528028	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002280	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0010821	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001508	PMID:36528028	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0100704	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0008551	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000618	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0100702	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002119	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000256	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001741	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000577	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001320	PMID:36528028	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002015	PMID:36528028	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000750	PMID:36528028	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000431	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001684	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001285	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0003186	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0002171	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0011344	PMID:36528028	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0100710	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0012168	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000505	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0200012	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000664	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0001357	PMID:36528028	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0200055	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0007018	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620455	Neurodevelopmental disorder with hypotonia and speech delay, with or without seizures		HP:0000347	PMID:36528028	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000044	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0003621	PMID:10022408	PCS		1/10			C	HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0003560	OMIM:300200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0003593	PMID:10022408	PCS		2/10			C	HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0008163	PMID:10022408	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000826	OMIM:300200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0001508	PMID:10022408	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0001419	PMID:10022408	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0011463	PMID:10022408	PCS		2/10			C	HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0008197	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0011462	PMID:23384712	PCS		3/3			C	HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0002902	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0001944	PMID:10022408	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000953	PMID:10022408	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000846	PMID:10022408	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000835	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000823	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0004319	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000127	PMID:10022408	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000798	PMID:23384712	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000028	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0008207	OMIM:300200	IEA					P	HPO:iea[2009-02-17]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0003623	PMID:10022408	PCS		5/10			C	HPO:probinson[2022-03-25]
OMIM:300200	Adrenal hypoplasia, congenital		HP:0000027	OMIM:300200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:140850	Hemangiomas, cavernous, of face and supraumbilical midline raphe		HP:0010309	PMID:10826620	PCS					P	HPO:nvasilevsky[2018-10-30]
OMIM:140850	Hemangiomas, cavernous, of face and supraumbilical midline raphe		HP:0410276	PMID:10826620	PCS					P	HPO:nvasilevsky[2018-10-30]
OMIM:140850	Hemangiomas, cavernous, of face and supraumbilical midline raphe		HP:0012020	PMID:10826620	PCS					P	HPO:nvasilevsky[2018-10-30]
OMIM:140850	Hemangiomas, cavernous, of face and supraumbilical midline raphe		HP:0001680	PMID:10826620	PCS					P	HPO:nvasilevsky[2018-10-30]
OMIM:140850	Hemangiomas, cavernous, of face and supraumbilical midline raphe		HP:0007486	OMIM:140850	IEA					P	HPO:iea[2009-02-17]
OMIM:140850	Hemangiomas, cavernous, of face and supraumbilical midline raphe		HP:0000006	OMIM:140850	IEA					I	HPO:iea[2009-02-17]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0025709	PMID:15784703	PCS		2/4			C	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0030795	PMID:15784703	PCS		4/4			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0011463	PMID:15784703	PCS		1/4			C	HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0008255	PMID:15784703	PCS		1/4			P	HPO:probinson[2013-01-09];HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0003593	PMID:15784703	PCS		1/4			C	HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0003074	PMID:15784703	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0040217	PMID:15784703	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0009800	PMID:15784703	PCS		1/2			H	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0000006	PMID:15784703	PCS					I	HPO:probinson[2013-02-28];HPO:probinson[2023-02-18]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0003623	OMIM:610582	TAS		HP:0040283			C	HPO:skoehler[2017-07-13]
OMIM:610582	Diabetes mellitus, transient neonatal, 3		HP:0025329	PMID:15784703	PCS		1/4			P	HPO:probinson[2023-02-18]
OMIM:600791	Deafness, autosomal recessive 4, with enlarged vestibular aqueduct		HP:0003577	PMID:9500541	PCS		10/10			C	HPO:probinson[2022-06-14]
OMIM:600791	Deafness, autosomal recessive 4, with enlarged vestibular aqueduct		HP:0000376	PMID:9500541	PCS		0/3			P	HPO:probinson[2013-04-01];HPO:probinson[2022-06-14]
OMIM:600791	Deafness, autosomal recessive 4, with enlarged vestibular aqueduct		HP:0011387	PMID:9500541	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-14]
OMIM:600791	Deafness, autosomal recessive 4, with enlarged vestibular aqueduct		HP:0000407	PMID:9500541	PCS	HP:0003577	10/10			P	HPO:probinson[2013-04-01];HPO:probinson[2022-06-14]
OMIM:600791	Deafness, autosomal recessive 4, with enlarged vestibular aqueduct		HP:0000007	PMID:9500541	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-06-14]
OMIM:600791	Deafness, autosomal recessive 4, with enlarged vestibular aqueduct		HP:0000853	PMID:9500541	PCS		0/10			P	HPO:probinson[2022-06-14]
OMIM:204700	Amelogenesis imperfecta, hypomaturation type, iia1		HP:0000670	OMIM:204700	TAS					P	HPO:skoehler[2015-04-05]
OMIM:204700	Amelogenesis imperfecta, hypomaturation type, iia1		HP:0000705	PMID:15235027	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-03-27]
OMIM:204700	Amelogenesis imperfecta, hypomaturation type, iia1		HP:0009102	PMID:15235027	PCS		1/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-03-27]
OMIM:204700	Amelogenesis imperfecta, hypomaturation type, iia1		HP:0006285	PMID:15235027	PCS		2/2			P	HPO:probinson[2023-03-27]
OMIM:204700	Amelogenesis imperfecta, hypomaturation type, iia1		HP:0006286	PMID:15235027	PCS		2/2			P	HPO:probinson[2023-03-27]
OMIM:204700	Amelogenesis imperfecta, hypomaturation type, iia1		HP:0003593	PMID:15235027	PCS		2/2			C	HPO:probinson[2023-03-27]
OMIM:204700	Amelogenesis imperfecta, hypomaturation type, iia1		HP:0000007	PMID:15235027	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2023-03-27]
OMIM:249600	Mietens-Weber syndrome		HP:0000486	OMIM:249600	IEA					P	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0000639	OMIM:249600	IEA					P	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0000460	OMIM:249600	TAS					P	HPO:probinson[2013-12-20]
OMIM:249600	Mietens-Weber syndrome		HP:0000007	OMIM:249600	IEA					I	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0008850	OMIM:249600	IEA					P	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0009821	OMIM:249600	IEA					P	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0003083	OMIM:249600	IEA					P	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0001763	OMIM:249600	IEA					P	HPO:skoehler[2010-06-20]
OMIM:249600	Mietens-Weber syndrome		HP:0002987	OMIM:249600	IEA					P	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0005093	OMIM:249600	IEA					P	HPO:iea[2009-02-17]
OMIM:249600	Mietens-Weber syndrome		HP:0001249	OMIM:249600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:614082	Fanconi anemia, complementation group G		HP:0000252	PMID:11093276	PCS		14/22			P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0001909	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0003220	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0001903	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0001172	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0000568	PMID:11093276	PCS		8/22			P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0007565	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0001873	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0001510	PMID:11093276	PCS		19/23			P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0002863	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:614082	Fanconi anemia, complementation group G		HP:0001875	PMID:11093276	PCS					P	HPO:probinson[2013-08-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0002267	PMID:36001086	PCS		3/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0003577	PMID:36001086	PCS		6/6			C	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0000486	PMID:36001086	PCS		1/5			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0000365	PMID:36001086	PCS		3/3			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0002120	PMID:36001086	PCS		1/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001272	PMID:36001086	PCS		3/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0032794	PMID:36001086	PCS	HP:0003623	4/4			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0002380	PMID:36001086	PCS		1/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0032398	PMID:36001086	PCS		4/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0012444	PMID:36001086	PCS		4/7			P	HPO:probinson[2023-07-10];HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0000639	PMID:36001086	PCS		2/5			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0000518	PMID:36001086	PCS		1/5			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0007068	PMID:36001086	PCS		1/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0002878	PMID:36001086	PCS		6/6			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001643	PMID:36001086	PCS		1/6			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0008936	PMID:36001086	PCS		3/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001321	PMID:36001086	PCS		1/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0003121	PMID:36001086	PCS		4/4			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001263	PMID:36001086	PCS		3/3			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0002509	PMID:36001086	PCS		4/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0000007	PMID:36001086	PCS					I	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001511	PMID:36001086	PCS		3/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001631	PMID:36001086	PCS		2/6			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001337	PMID:36001086	PCS		1/7			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0000028	PMID:36001086	PCS		3/4			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0001655	PMID:36001086	PCS		1/6			P	HPO:probinson[2023-07-10]
OMIM:620327	Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities		HP:0000126	PMID:36001086	PCS		1/6			P	HPO:probinson[2023-07-10]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0003676	PMID:28575651	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001332	PMID:29388673	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001272	PMID:28575651	PCS		4/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001250	PMID:29388673	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001252	PMID:28575651;PMID:29388673	PCS		10/10			P	HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001251	PMID:28575651	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0003593	PMID:28575651;PMID:29388673	PCS		11/17			C	ORCID:0000-0002-0736-9199[2024-05-01];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001270	PMID:28575651;PMID:29388673	PCS		18/18			P	ORCID:0000-0002-0736-9199[2024-05-01];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0012444	PMID:29388673	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0033747	PMID:28575651	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0033725	PMID:28575651;PMID:29388673	PCS		6/14			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0100543	PMID:28575651	PCS		2/7			P	HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000639	PMID:28575651;PMID:29388673	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-05-01];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0011463	PMID:28575651;PMID:29388673	PCS		5/17			C	HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000414	PMID:29388673	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000678	PMID:29388673	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0003429	PMID:28575651;PMID:29388673	PCS		13/15			P	HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000218	PMID:29388673	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0007941	PMID:28575651	PCS		2/7			P	HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000212	PMID:29388673	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002415	PMID:28575651	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002599	PMID:28575651	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001347	PMID:28575651;PMID:29388673	PCS		9/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-07];ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0003623	PMID:29388673	PCS		1/10			C	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000473	PMID:28575651	PCS		3/7			P	HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0025331	PMID:28575651	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000571	PMID:28575651	PCS		5/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0003621	PMID:28575651	PCS		1/7			C	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002650	PMID:29388673	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002078	PMID:28575651	PCS		5/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002376	PMID:29388673	PCS		4/6			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000276	PMID:29388673	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001260	PMID:28575651	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07];HPO:probinson[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002451	PMID:28575651	PCS		4/7			P	HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001263	PMID:28575651;PMID:29388673	PCS		11/16			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002070	PMID:28575651	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0011344	PMID:28575651	PCS		2/7			P	HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0034392	PMID:29388673	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000668	PMID:29388673	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0007256	PMID:28575651	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000007	PMID:28575651	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-03-07]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002505	PMID:28575651	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0002007	PMID:29388673	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0000664	PMID:29388673	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:617560	Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy		HP:0001257	PMID:28575651;PMID:29388673	PCS		16/16			P	ORCID:0000-0002-0736-9199[2024-05-01];HPO:skoehler[2018-10-08];HPO:probinson[2022-03-07]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000286	PMID:31422817	PCS		3/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0002188	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000486	PMID:31422817	PCS		3/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001252	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0100694	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000319	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000316	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001845	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001249	PMID:31422817	IEA		4/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0002553	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000252	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000054	PMID:31422817	PCS		1/2	MALE		P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0030148	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0002079	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0011968	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001263	PMID:31422817	PCS		4/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0004691	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001182	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0031632	PMID:31422817	PCS		1/3			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0004409	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0005616	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000125	PMID:31422817	PCS		1/4		HP:0012833	P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000369	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000006	PMID:31422817	PCS					I	HPO:probinson[2020-12-01]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000126	PMID:31422817	PCS	HP:0003577	1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001655	PMID:31422817	PCS		2/3			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000341	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0009916	PMID:31422817	PCS		1/4		HP:0012825	P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000540	PMID:31422817	PCS		3/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000023	PMID:31422817	PCS					P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001195	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0002719	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000733	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000218	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0002558	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001545	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0008936	PMID:31422817	PCS		1/4		HP:0012825	P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001562	PMID:31422817	PCS	HP:0011461	1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000396	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000076	PMID:31422817	PCS	HP:0003577	1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000992	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000750	PMID:31422817	PCS		4/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0002650	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001288	PMID:31422817	PCS		3/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000270	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0045025	PMID:31422817	PCS		2/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0002007	PMID:31422817	PCS		1/4			P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0000028	PMID:31422817	PCS		1/2	MALE		P	HPO:probinson[2020-07-17]
OMIM:618653	Intellectual developmental disorder with impaired language and dysmorphic facies		HP:0001513	PMID:31422817	PCS		2/4		HP:0012825	P	HPO:probinson[2020-07-17]
OMIM:615377	Atrial fibrillation, familial, 13		HP:0001650	PMID:19808477	PCS		1/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-07-10]
OMIM:615377	Atrial fibrillation, familial, 13		HP:0003596	PMID:19808477	PCS		2/2			C	HPO:probinson[2022-07-10]
OMIM:615377	Atrial fibrillation, familial, 13		HP:0031295	PMID:19808477	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-10]
OMIM:615377	Atrial fibrillation, familial, 13		HP:0004757	PMID:19808477	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-07-10]
OMIM:615377	Atrial fibrillation, familial, 13		HP:0000006	PMID:19808477	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-10]
OMIM:613706	Noonan syndrome 7		HP:0000341	PMID:19206169	PCS		3/5			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000286	PMID:19206169	PCS		0/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000486	PMID:19206169	PCS		3/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0004322	PMID:19206169	PCS		5/5			P	HPO:probinson[2013-06-02];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001250	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001054	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001252	OMIM:613706	TAS					P	HPO:probinson[2013-06-02]
OMIM:613706	Noonan syndrome 7		HP:0002162	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0030939	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001290	PMID:19206169	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0006191	PMID:19206169	PCS		1/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0100543	OMIM:613706	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613706	Noonan syndrome 7		HP:0000914	PMID:19206169	PCS		3/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0012471	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0011220	PMID:19206169	PCS		4/5			P	HPO:probinson[2013-06-02];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000316	PMID:19206169	PCS		5/5			P	HPO:probinson[2013-06-02];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000975	PMID:19206169	PCS		1/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0008872	OMIM:613706	TAS					P	HPO:probinson[2013-06-02]
OMIM:613706	Noonan syndrome 7		HP:0001642	PMID:19206169	PCS		3/10			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24];HPO:probinson[2013-06-02];HPO:probinson[2021-05-22]
OMIM:613706	Noonan syndrome 7		HP:0000256	PMID:19206169	PCS		5/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0009748	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001249	PMID:19206169	PCS		5/5			P	HPO:probinson[2013-06-02];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0002212	PMID:19206169	PCS		1/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0002015	OMIM:613706	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613706	Noonan syndrome 7		HP:0000494	PMID:19206169	PCS		3/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0002650	PMID:19206169	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-10]
OMIM:613706	Noonan syndrome 7		HP:0001520	PMID:19206169	PCS		2/4			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001382	PMID:19206169	PCS		3/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000391	PMID:19206169	PCS		4/5			P	HPO:probinson[2013-06-02];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0002033	PMID:19206169	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000470	PMID:19206169	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-10]
OMIM:613706	Noonan syndrome 7		HP:0002031	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0012059	PMID:19206169	PCS		3/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0005280	PMID:19206169	PCS		3/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0011470	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0031162	PMID:19206169	PCS		4/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001639	PMID:19206169	PCS		0/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000767	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000768	PMID:19206169	PCS					P	HPO:skoehler[2018-10-08];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0002967	PMID:19206169	PCS		3/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000306	PMID:19206169	PCS		2/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000268	OMIM:613706	TAS					P	HPO:probinson[2013-06-02]
OMIM:613706	Noonan syndrome 7		HP:0000465	PMID:19206169	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001510	PMID:19206169	PCS	HP:0003623	5/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0001631	PMID:19206169	PCS		1/5			P	HPO:lccarmody[2019-05-24];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000369	PMID:19206169	PCS		4/5			P	HPO:probinson[2013-06-02];HPO:lccarmody[2019-05-24]
OMIM:613706	Noonan syndrome 7		HP:0000006	PMID:19206169	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2020-08-10]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000286	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0003577	OMIM:614069	TAS					C	HPO:skoehler[2013-04-02]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000463	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0003196	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0001270	PMID:21596365	PCS		4/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0002719	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000316	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000218	OMIM:614069	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0020102	PMID:21596365	PCS		2/7			P	HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000278	OMIM:614069	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000311	OMIM:614069	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0001249	PMID:21596365	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0004315	PMID:21596365	PCS		7/7			P	HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0002850	PMID:21596365	PCS		6/7			P	HPO:probinson[2023-03-24];HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0002014	PMID:21596365	PCS		2/7			P	HPO:probinson[2023-03-24];HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0004313	PMID:21596365	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0005401	PMID:21596365	PCS		2/7			P	HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000331	OMIM:614069	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0001263	PMID:21596365	PCS					P	HPO:probinson[2023-03-24];HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0002090	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0005280	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0010976	PMID:21596365	PCS		4/8			P	HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000007	OMIM:614069	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0002788	PMID:21596365	PCS		14/14			P	HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0001510	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0000369	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0002720	PMID:21596365	PCS		5/7			P	HPO:probinson[2023-03-24]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0004469	OMIM:614069	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614069	Immunodeficiency-Centromeric instability-facial anomalies syndrome2		HP:0002721	OMIM:614069	IEA					P	HPO:skoehler[2015-01-27]
OMIM:613060	Epilepsy, idiopathic generalized, 10		HP:0002069	OMIM:613060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613060	Epilepsy, idiopathic generalized, 10		HP:0002123	OMIM:613060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613060	Epilepsy, idiopathic generalized, 10		HP:0002373	OMIM:613060	TAS	HP:0003593				P	HPO:skoehler[2012-10-17]
OMIM:613060	Epilepsy, idiopathic generalized, 10		HP:0002373	PMID:15115768	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:613060	Epilepsy, idiopathic generalized, 10		HP:0002121	OMIM:613060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613060	Epilepsy, idiopathic generalized, 10		HP:0007359	OMIM:613060	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613060	Epilepsy, idiopathic generalized, 10		HP:0000006	PMID:15115768	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:211480	Buerger disease		HP:0012531	OMIM:211480	TAS					P	HPO:skoehler[2014-01-28]
OMIM:211480	Buerger disease		HP:0030880	OMIM:211480	TAS					P	HPO:skoehler[2017-07-13]
OMIM:211480	Buerger disease		HP:0000007	OMIM:211480	IEA					I	HPO:iea[2009-02-17]
OMIM:211480	Buerger disease		HP:0000975	OMIM:211480	IEA					P	HPO:skoehler[2009-02-17]
OMIM:211480	Buerger disease		HP:0009763	OMIM:211480	IEA					P	HPO:skoehler[2009-02-17]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0002510	OMIM:615411	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0000252	PMID:23603762	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0032409	PMID:23603762	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0002079	PMID:23603762	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0001250	PMID:23603762	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0001263	PMID:23603762	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0002282	OMIM:615411	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0031882	PMID:23603762	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0033725	PMID:23603762	PCS		2/2			P	HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0000639	OMIM:615411	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0001339	OMIM:615411	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0002539	OMIM:615411	IEA					P	HPO:skoehler[2015-01-19]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0001302	PMID:23603762	PCS		2/2			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-01]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0001511	OMIM:615411	TAS		HP:0040283			P	HPO:skoehler[2013-10-06]
OMIM:615411	Cortical dysplasia, complex, with other brain malformations 3		HP:0000006	PMID:23603762	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-03-01]
OMIM:616118	Macular degeneration, early-onset		HP:0011506	PMID:24899048	PCS	HP:0011462	1/4			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-20]
OMIM:616118	Macular degeneration, early-onset		HP:0000608	PMID:24899048	PCS		4/4			P	HPO:skoehler[2015-01-21];HP:probinson[2019-01-20]
OMIM:616118	Macular degeneration, early-onset		HP:0007663	PMID:24899048	PCS					P	HPO:skoehler[2015-07-26];HP:probinson[2019-01-20]
OMIM:616118	Macular degeneration, early-onset		HP:0000006	PMID:24899048	PCS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-20]
OMIM:616118	Macular degeneration, early-onset		HP:0011842	PMID:24899048	PCS		0/4			P	HP:probinson[2019-01-20];HPO:probinson[2023-04-09]
OMIM:607015	Hurler-Scheie syndrome		HP:0007957	PMID:22210666	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0004322	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0000023	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0100490	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0002240	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0003393	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0001072	OMIM:607015	IEA					P	HPO:skoehler[2019-04-18]
OMIM:607015	Hurler-Scheie syndrome		HP:0011463	PMID:22210666	PCS		1/1			C	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0012471	OMIM:607015	TAS					P	HPO:skoehler[2014-11-26]
OMIM:607015	Hurler-Scheie syndrome		HP:0002777	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0001744	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0001007	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0002159	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0002650	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0002870	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0001387	PMID:22210666	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0002092	OMIM:607015	TAS				HP:0012825	P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0005280	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0002808	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0001537	PMID:22210666	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0000943	PMID:22210666	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0008301	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0009697	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0000007	PMID:22210666	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0001659	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0002205	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0001653	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:607015	Hurler-Scheie syndrome		HP:0046505	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0001510	PMID:22210666	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:607015	Hurler-Scheie syndrome		HP:0000347	OMIM:607015	TAS					P	HPO:skoehler[2014-01-28]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0003236	PMID:27066570	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0003621	PMID:27066570	PCS		1/3			C	HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0000750	PMID:27066570	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0003693	PMID:27066570	PCS		1/3			P	HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0008981	PMID:27066570	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0001263	PMID:27066570	PCS		1/3			P	HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0003593	PMID:27066570	PCS		2/3			C	HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0000007	PMID:27066570	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0001270	PMID:27066570	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0003391	PMID:27066570	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0003701	PMID:27066570	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-12]
OMIM:618135	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8		HP:0001249	PMID:27066570	PCS		2/3			P	HPO:probinson[2023-02-12]
OMIM:223340	Dk phocomelia syndrome		HP:0009829	OMIM:223340	IEA					P	HPO:iea[2009-02-17]
OMIM:223340	Dk phocomelia syndrome		HP:0000007	OMIM:223340	IEA					I	HPO:iea[2009-02-17]
OMIM:223340	Dk phocomelia syndrome		HP:0002084	OMIM:223340	IEA					P	HPO:iea[2009-02-17]
OMIM:223340	Dk phocomelia syndrome		HP:0000119	OMIM:223340	IEA					P	HPO:iea[2009-02-17]
OMIM:223340	Dk phocomelia syndrome		HP:0001873	OMIM:223340	IEA					P	HPO:iea[2009-02-17]
OMIM:175800	Porokeratosis 1, multiple types		HP:0003621	PMID:26202976	PCS					C	HPO:probinson[2022-09-08]
OMIM:175800	Porokeratosis 1, multiple types		HP:0001036	PMID:26202976	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-08]
OMIM:175800	Porokeratosis 1, multiple types		HP:0011462	PMID:26202976	PCS					C	HPO:probinson[2022-09-08]
OMIM:175800	Porokeratosis 1, multiple types		HP:0200044	PMID:26202976	PCS		9/9			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-08]
OMIM:175800	Porokeratosis 1, multiple types		HP:0000006	PMID:26202976	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-08]
OMIM:122780	Coxoauricular syndrome		HP:0000365	OMIM:122780	IEA					P	HPO:iea[2009-02-17]
OMIM:122780	Coxoauricular syndrome		HP:0004322	OMIM:122780	IEA					P	HPO:iea[2009-02-17]
OMIM:122780	Coxoauricular syndrome		HP:0002827	OMIM:122780	IEA					P	HPO:iea[2009-02-17]
OMIM:122780	Coxoauricular syndrome		HP:0008551	OMIM:122780	IEA					P	HPO:iea[2009-02-17]
OMIM:122780	Coxoauricular syndrome		HP:0001423	OMIM:122780	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:122780	Coxoauricular syndrome		HP:0000006	OMIM:122780	TAS					I	HPO:nvasilevsky[2019-03-11]
OMIM:613074	Deafness, autosomal dominant 50		HP:0000408	OMIM:613074	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613074	Deafness, autosomal dominant 50		HP:0000407	PMID:19363479	PCS					P	HPO:probinson[2013-04-14]
OMIM:613074	Deafness, autosomal dominant 50		HP:0000360	OMIM:613074	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:613074	Deafness, autosomal dominant 50		HP:0001730	PMID:19363479	PCS					P	HPO:probinson[2013-04-14]
OMIM:613074	Deafness, autosomal dominant 50		HP:0000006	PMID:19363479	PCS					I	HPO:probinson[2013-01-09]
OMIM:186750	Talonavicular coalition		HP:0010109	PMID:29270563	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:186750	Talonavicular coalition		HP:0009177	OMIM:186750	IEA					P	HPO:iea[2009-02-17]
OMIM:186750	Talonavicular coalition		HP:0025238	PMID:29270563	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:186750	Talonavicular coalition		HP:0004209	OMIM:186750	IEA					P	HPO:iea[2009-02-17]
OMIM:186750	Talonavicular coalition		HP:0005802	PMID:29270563	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:186750	Talonavicular coalition		HP:0000006	OMIM:186750	IEA					I	HPO:iea[2009-02-17]
OMIM:186750	Talonavicular coalition		HP:0003028	PMID:29270563	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:615363	Estrogen resistance		HP:0003621	PMID:23841731	PCS		1/1			C	HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0031428	PMID:23841731	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0010639	PMID:23841731	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0000013	PMID:23841731	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0002750	PMID:23841731	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0025134	PMID:23841731	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0040270	OMIM:615363	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615363	Estrogen resistance		HP:0001061	PMID:23841731	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0100783	PMID:23841731	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0000938	PMID:23841731	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0000007	PMID:23841731	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0000956	OMIM:615363	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615363	Estrogen resistance		HP:0000823	PMID:23841731	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0000147	PMID:23841731	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0000842	OMIM:615363	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615363	Estrogen resistance		HP:0000786	PMID:23841731	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-01-23]
OMIM:615363	Estrogen resistance		HP:0001952	OMIM:615363	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613712	Hirschsprung disease, susceptibility to, 4		HP:0003577	PMID:9359047;PMID:10231870	PCS		2/2			C	HPO:probinson[2022-12-13]
OMIM:613712	Hirschsprung disease, susceptibility to, 4		HP:0002251	PMID:9359047;PMID:10231870	PCS		2/2			P	HPO:probinson[2022-12-13];HPO:skoehler[2018-10-08];HPO:probinson[2022-12-13]
OMIM:613712	Hirschsprung disease, susceptibility to, 4		HP:0000006	PMID:9359047	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-13]
OMIM:617574	Ichthyosis, congenital, autosomal recessive 13		HP:0003577	PMID:28173123	PCS					C	HPO:probinson[2023-03-12]
OMIM:617574	Ichthyosis, congenital, autosomal recessive 13		HP:0008064	PMID:28173123	PCS					P	HPO:probinson[2023-03-12]
OMIM:617574	Ichthyosis, congenital, autosomal recessive 13		HP:0025114	PMID:28173123	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617574	Ichthyosis, congenital, autosomal recessive 13		HP:0000007	PMID:28173123	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-03-12]
OMIM:617574	Ichthyosis, congenital, autosomal recessive 13		HP:0000972	PMID:28173123	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617574	Ichthyosis, congenital, autosomal recessive 13		HP:0012203	PMID:28173123	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-12]
OMIM:617574	Ichthyosis, congenital, autosomal recessive 13		HP:0000962	PMID:28173123	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:182250	Singleton-Merten syndrome 1		HP:0004325	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001650	OMIM:182250	TAS					P	HPO:skoehler[2012-10-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0004322	PMID:23322711	PCS		6/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001252	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0003593	PMID:23322711	PCS		2/11			C	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0100295	OMIM:182250	IEA					P	HPO:skoehler[2018-10-08]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001290	OMIM:182250	TAS					P	HPO:skoehler[2017-07-13]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000319	PMID:23322711	PCS		7/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0011463	PMID:23322711	PCS		7/11			C	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0011462	PMID:23322711	PCS		1/11			C	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001806	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0006353	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0006232	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0006112	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002857	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001324	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0005303	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002673	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0009890	OMIM:182250;PMID:23322711	PCS		17/17			P	HPO:probinson[2022-05-29];HPO:skoehler[2015-05-31]
OMIM:182250	Singleton-Merten syndrome 1		HP:0009771	OMIM:182250;PMID:23322711	PCS		16/19			P	HPO:probinson[2022-05-29];HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002827	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0006386	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000327	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000006	PMID:25620204	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002202	PMID:23322711	PCS		3/11			P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002684	PMID:23322711	PCS		10/11			P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0004382	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0004380	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0100550	OMIM:182250	TAS					P	HPO:skoehler[2015-05-31]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000939	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000938	PMID:23322711	PCS		10/11			P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0030043	OMIM:182250	TAS					P	HPO:skoehler[2015-01-20]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000337	PMID:23322711	PCS		7/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002515	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000219	PMID:23322711	PCS		7/7			P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0006336	PMID:23322711	PCS		10/11			P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001682	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0003621	PMID:23322711	PCS		1/11			C	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000670	PMID:23322711	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001762	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000992	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002650	PMID:23322711	PCS		3/11			P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001761	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001640	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0003182	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0032153	PMID:23322711	PCS		8/9			P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000706	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000508	PMID:23322711	PCS		7/7		HP:0012825	P	HPO:probinson[2022-05-29]
OMIM:182250	Singleton-Merten syndrome 1		HP:0008102	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0001635	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0002205	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000545	OMIM:182250	IEA					P	HPO:iea[2009-02-17]
OMIM:182250	Singleton-Merten syndrome 1		HP:0000501	PMID:23322711	PCS		5/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-29]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0003202	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001265	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0003477	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0003487	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001371	OMIM:611105	TAS					P	HPO:skoehler[2015-12-30]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001260	OMIM:611105	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0002352	OMIM:611105	TAS					P	HPO:skoehler[2015-01-21]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001251	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001270	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0100543	OMIM:611105	TAS		HP:0040283			P	HPO:skoehler[2014-04-04]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0000639	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0003828	OMIM:611105	TAS					M	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0000007	OMIM:611105	TAS					I	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001324	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001257	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0003677	OMIM:611105	TAS					C	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001337	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611105	Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation		HP:0001347	OMIM:611105	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601316	Deafness, autosomal dominant nonsyndromic sensorineural 10		HP:0000407	OMIM:601316	TAS					P	HPO:probinson[2013-03-12]
OMIM:601316	Deafness, autosomal dominant nonsyndromic sensorineural 10		HP:0000006	OMIM:601316	TAS					I	HPO:probinson[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0006548	PMID:16542389;PMID:18312453;PMID:12920067;PMID:19270816	PCS		29/65			P	HPO:probinson[2022-03-07];HPO:iea[2009-02-17];HPO:probinson[2020-05-07];HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001694	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001250	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002140	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0011934	OMIM:187300	TAS					P	HPO:probinson[2012-06-10]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0012151	PMID:30057878	PCS					P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001009	PMID:18312453	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001722	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0000434	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002138	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001342	OMIM:187300	TAS					P	HPO:probinson[2012-04-25]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0005268	PMID:12920067	PCS		8/28	FEMALE		C	HPO:probinson[2020-05-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002076	PMID:12920067	PCS		20/49			P	HPO:iea[2009-02-17];HPO:probinson[2020-05-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0012418	PMID:30336550	PCS					P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002390	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0100585	PMID:19270816	PCS		2/2			P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0040223	PMID:30057878	PCS					P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0100858	OMIM:187300	TAS					P	HPO:probinson[2012-06-10]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002629	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002707	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001217	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0000524	OMIM:187300	TAS					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002626	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0000961	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0004406	OMIM:187300	IEA	HP:0003621				P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0004406	PMID:12920067	PCS	HP:0011463	48/49			P	HPO:probinson[2020-05-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0004406	PMID:16542389	PCS		13/13			P	HPO:probinson[2022-03-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0004406	PMID:18312453	PCS		1/1			P	HPO:probinson[2022-03-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0000006	PMID:12920067	PCS					I	HPO:probinson[2012-04-25];HPO:probinson[2020-05-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0006107	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002105	PMID:19364794	PCS		1/1			P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001232	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002642	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001394	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0030877	PMID:17220751	PCS		11/126			P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001903	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0006574	PMID:19270816	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0100749	PMID:17641482	PCS					P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0001901	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002239	PMID:16542389	PCS		1/13			P	HPO:probinson[2022-03-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002875	PMID:17641482	PCS					P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0000214	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0030049	PMID:1518020	PCS					P	HPO:skoehler[2014-09-21];HPO:probinson[2020-05-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002573	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0000471	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002094	OMIM:187300;PMID:30057878	PCS		20/20			P	HPO:probinson[2020-11-18];HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0032542	PMID:30057878	PCS					M	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002092	PMID:26015855	PCS					P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002091	PMID:17220751	PCS		19/126			P	HPO:probinson[2020-11-18]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0025709	PMID:18312453	PCS		1/1			C	HPO:probinson[2022-03-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002408	PMID:16542389;PMID:12920067	PCS		5/62			P	HPO:probinson[2022-03-07];HPO:iea[2009-02-17];HPO:probinson[2020-05-07]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0000227	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002604	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002249	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002326	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:187300	Telangiectasia, hereditary hemorrhagic, type 1		HP:0002248	OMIM:187300	IEA					P	HPO:iea[2009-02-17]
OMIM:614055	Acetyl-Coa acetyltransferase-2 deficiency		HP:0003542	OMIM:614055	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614055	Acetyl-Coa acetyltransferase-2 deficiency		HP:0002151	OMIM:614055	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614055	Acetyl-Coa acetyltransferase-2 deficiency		HP:0001263	OMIM:614055	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614055	Acetyl-Coa acetyltransferase-2 deficiency		HP:0001252	OMIM:614055	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614055	Acetyl-Coa acetyltransferase-2 deficiency		HP:0002072	OMIM:614055	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614055	Acetyl-Coa acetyltransferase-2 deficiency		HP:0001290	OMIM:614055	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614055	Acetyl-Coa acetyltransferase-2 deficiency		HP:0003745	OMIM:614055	TAS					I	HPO:skoehler[2015-12-30]
OMIM:603529	Dyserythropoiesis, congenital, with ultrastructurally normal erythroblastheterochromatin		HP:0011273	OMIM:603529	TAS					P	HPO:skoehler[2014-03-24]
OMIM:603529	Dyserythropoiesis, congenital, with ultrastructurally normal erythroblastheterochromatin		HP:0010972	OMIM:603529	TAS					P	HPO:skoehler[2014-03-24]
OMIM:603529	Dyserythropoiesis, congenital, with ultrastructurally normal erythroblastheterochromatin		HP:0032566	PMID:9858240	PCS					P	HPO:probinson[2019-09-07]
OMIM:603529	Dyserythropoiesis, congenital, with ultrastructurally normal erythroblastheterochromatin		HP:0000006	OMIM:603529	TAS					I	HPO:skoehler[2014-03-24]
OMIM:603529	Dyserythropoiesis, congenital, with ultrastructurally normal erythroblastheterochromatin		HP:0004447	OMIM:603529	TAS					P	HPO:skoehler[2014-03-24]
OMIM:606451	Deafness, autosomal dominant 30		HP:0000407	PMID:11571554	PCS					P	HPO:probinson[2019-04-20]
OMIM:606451	Deafness, autosomal dominant 30		HP:0000006	PMID:11571554	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-04-20]
OMIM:118420	Chiari malformation type I		HP:0000365	OMIM:118420	TAS					P	HPO:probinson[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0002321	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0003396	OMIM:118420	TAS					P	HPO:probinson[2013-03-30]
OMIM:118420	Chiari malformation type I		HP:0002066	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0000020	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0000360	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0002061	OMIM:118420	TAS					P	HPO:probinson[2013-03-30]
OMIM:118420	Chiari malformation type I		HP:0003690	OMIM:118420	IEA					P	HPO:skoehler[2010-06-20]
OMIM:118420	Chiari malformation type I		HP:0030833	OMIM:118420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:118420	Chiari malformation type I		HP:0000639	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0000613	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0002317	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0002315	OMIM:118420	TAS					P	HPO:probinson[2013-03-30]
OMIM:118420	Chiari malformation type I		HP:0002015	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0003401	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0000651	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0002650	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0003487	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0002395	OMIM:118420	TAS					P	HPO:skoehler[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0001260	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0012046	OMIM:118420	TAS					P	HPO:probinson[2013-03-30]
OMIM:118420	Chiari malformation type I		HP:0007099	OMIM:118420	TAS					P	HPO:skoehler[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0010780	OMIM:118420	IEA					P	HPO:skoehler[2010-06-18]
OMIM:118420	Chiari malformation type I		HP:0005759	OMIM:118420	IEA					P	HPO:iea[2009-02-17]
OMIM:118420	Chiari malformation type I		HP:0005758	OMIM:118420	TAS					P	HPO:skoehler[2013-10-22]
OMIM:118420	Chiari malformation type I		HP:0000006	OMIM:118420	IEA					I	HPO:iea[2009-02-17]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0005766	PMID:33568816	PCS		3/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0011939	PMID:33568816	PCS		3/3			P	HPO:probinson[2024-07-22]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0000076	PMID:33568816	PCS		1/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0003038	PMID:33568816	PCS		3/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0010621	PMID:33568816	PCS		3/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0033976	PMID:33568816	PCS		3/3			P	HPO:probinson[2021-07-16]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0010645	PMID:33568816	PCS		3/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0031260	PMID:33568816	PCS		3/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0040187	PMID:33568816	PCS		1/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0006077	PMID:33568816	PCS		1/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0001537	PMID:33568816	PCS		2/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0009577	PMID:33568816	PCS		1/3			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0000007	PMID:33568816	PCS					I	HPO:probinson[2021-05-18];HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0000059	PMID:33568816	PCS		1/1			P	HPO:probinson[2021-05-18]
OMIM:619217	Endove syndrome, Limb-Only type		HP:0000126	PMID:33568816	PCS		1/3			P	HPO:probinson[2021-05-18]
OMIM:274230	Thymoma, familial		HP:0002664	OMIM:274230	IEA					P	HPO:iea[2009-02-17]
OMIM:274230	Thymoma, familial		HP:0100522	OMIM:274230	TAS					P	HPO:skoehler[2012-10-17]
OMIM:274230	Thymoma, familial		HP:0001442	OMIM:274230	TAS					I	HPO:skoehler[2015-12-30]
OMIM:274230	Thymoma, familial		HP:0000007	OMIM:274230	IEA					I	HPO:iea[2009-02-17]
OMIM:274230	Thymoma, familial		HP:0002093	OMIM:274230	IEA					P	HPO:iea[2009-02-17]
OMIM:183600	Split-Hand/foot malformation 1		HP:0001199	OMIM:183600	TAS					P	HPO:skoehler[2015-01-04]
OMIM:183600	Split-Hand/foot malformation 1		HP:0000175	OMIM:183600	PCS		HP:0040282			P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0000365	PMID:16688749	PCS		35%			P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0001171	OMIM:183600	PCS		HP:0040281			P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0009380	PMID:16688749	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:183600	Split-Hand/foot malformation 1		HP:0100257	OMIM:183600	TAS					P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0001849	PMID:16688749	PCS		HP:0040282			P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0010055	OMIM:183600	TAS					P	HPO:skoehler[2015-01-04]
OMIM:183600	Split-Hand/foot malformation 1		HP:0003828	OMIM:183600	TAS					M	HPO:skoehler[2015-12-30]
OMIM:183600	Split-Hand/foot malformation 1		HP:0001839	OMIM:183600	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:183600	Split-Hand/foot malformation 1		HP:0003829	OMIM:183600	TAS					I	HPO:skoehler[2015-12-30]
OMIM:183600	Split-Hand/foot malformation 1		HP:0030680	PMID:16688749	PCS		13%			P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0030084	OMIM:183600	TAS					P	HPO:skoehler[2015-01-04]
OMIM:183600	Split-Hand/foot malformation 1		HP:0001159	PMID:16688749	IEA		HP:0040282			P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0000377	PMID:16688749	PCS		35%			P	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0000006	PMID:16688749	PCS					I	HPO:iea[2010-08-13]
OMIM:183600	Split-Hand/foot malformation 1		HP:0001249	PMID:16688749	PCS		33%			P	HPO:iea[2010-08-13]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000483	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000486	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000321	PMID:29276005	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000023	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0002066	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0003593	PMID:29276005	PCS		1/3			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0009185	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0011343	PMID:29276005	PCS		2/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000319	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000718	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000414	OMIM:618109	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0002317	OMIM:618109	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0009765	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0002558	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000377	OMIM:618109	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0003623	PMID:29276005	IEA		2/3			C	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000494	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000233	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000750	OMIM:618109	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0001684	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0002079	OMIM:618109	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0031936	OMIM:618109	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0005487	OMIM:618109	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0011968	PMID:29276005	PCS	HP:0003623	2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0001263	OMIM:618109	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0011344	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0009276	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000508	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000426	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0001338	PMID:29276005	PCS		1/3			P	HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000007	PMID:29276005	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000268	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000047	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0001631	OMIM:618109	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000545	PMID:29276005	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:618109	Intellectual developmental disorder, autosomal recessive 65		HP:0000028	PMID:29276005	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-30]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0003236	PMID:22683087	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0004322	PMID:22683087	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001250	PMID:22683087	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0005575	PMID:22683087	PCS		1/4			P	HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001252	PMID:22683087	PCS		4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0002240	PMID:22683087	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0100252	PMID:22683087	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0100255	PMID:22683087	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0031964	PMID:22683087	PCS		3/4			P	HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0000939	PMID:22683087	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001508	PMID:22683087	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0002656	OMIM:614727	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001324	OMIM:614727	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0000358	OMIM:614727	TAS					P	HPO:skoehler[2015-01-04]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0002751	OMIM:614727	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0031956	PMID:22683087	PCS		4/4			P	HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001382	PMID:22683087	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001263	OMIM:614727	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0000272	PMID:22683087	PCS		3/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0005484	PMID:22683087	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0011800	OMIM:614727	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0000705	OMIM:614727	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001955	PMID:22683087	PCS		1/4			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0000007	PMID:22683087	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001510	PMID:22683087	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0001873	PMID:22683087	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-29]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0002500	OMIM:614727	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614727	Congenital disorder of glycosylation, type IIK		HP:0000369	OMIM:614727	TAS					P	HPO:skoehler[2015-01-04]
OMIM:612356	Heparin cofactor II deficiency		HP:0004850	OMIM:612356	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612356	Heparin cofactor II deficiency		HP:0005521	OMIM:612356	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612356	Heparin cofactor II deficiency		HP:0004761	OMIM:612356	TAS					P	HPO:skoehler[2010-06-19]
OMIM:612356	Heparin cofactor II deficiency		HP:0000006	OMIM:612356	TAS					I	HPO:skoehler[2010-06-19]
OMIM:615439	Macular degeneration, age-related, 13		HP:0011506	OMIM:615439	IEA		10/20			P	HPO:skoehler[2018-10-08]
OMIM:615439	Macular degeneration, age-related, 13		HP:0000529	OMIM:615439	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615439	Macular degeneration, age-related, 13		HP:0000608	OMIM:615439	TAS					P	HPO:skoehler[2015-01-21]
OMIM:615439	Macular degeneration, age-related, 13		HP:0011510	OMIM:615439	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615439	Macular degeneration, age-related, 13		HP:0200056	OMIM:615439	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615439	Macular degeneration, age-related, 13		HP:0000006	OMIM:615439	TAS					I	HPO:skoehler[2013-10-22]
OMIM:619203	Premature ovarian failure 18		HP:0008209	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0025709	PMID:33508233	PCS		1/1			C	HPO:probinson[2022-08-27]
OMIM:619203	Premature ovarian failure 18		HP:0000013	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0000858	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0000869	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0011969	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0008232	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0000007	PMID:33508233	PCS					I	HPO:probinson[2021-03-30];HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0031103	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:619203	Premature ovarian failure 18		HP:0008724	PMID:33508233	PCS		1/1			P	HPO:probinson[2021-03-30]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0002322	PMID:36073231	PCS		2/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0003621	PMID:36073231	PCS		4/4			C	HPO:probinson[2024-02-11];HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0012452	PMID:36073231	PCS		1/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0002067	PMID:36073231	PCS		3/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0000716	PMID:36073231	PCS		1/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0002063	PMID:36073231	PCS		1/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0000739	PMID:36073231	PCS		1/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0000734	PMID:36073231	PCS		1/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0000007	PMID:36073231	PCS					I	HPO:probinson[2024-02-11];HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0002548	PMID:36073231	PCS		4/4			P	HPO:probinson[2024-02-11];HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0002307	PMID:36073231	PCS		1/4			P	HPO:probinson[2024-02-11]
OMIM:620482	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development		HP:0001249	PMID:36073231	PCS		4/4			P	HPO:probinson[2024-02-11]
OMIM:610227	Seborrhea-Like dermatitis with psoriasiform elements		HP:0032152	PMID:16751772	PCS					P	HPO:probinson[2022-02-27]
OMIM:610227	Seborrhea-Like dermatitis with psoriasiform elements		HP:0001051	PMID:16751772	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2022-02-27]
OMIM:610227	Seborrhea-Like dermatitis with psoriasiform elements		HP:0025092	PMID:16751772	PCS					P	HPO:probinson[2022-02-27]
OMIM:610227	Seborrhea-Like dermatitis with psoriasiform elements		HP:0000006	PMID:16751772	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-02-27]
OMIM:610227	Seborrhea-Like dermatitis with psoriasiform elements		HP:0000962	PMID:16751772	PCS					P	HPO:probinson[2013-04-01];HPO:probinson[2022-02-27]
OMIM:606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS		HP:0002850	OMIM:606445	TAS					P	HPO:skoehler[2013-05-07]
OMIM:606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS		HP:0002719	OMIM:606445	TAS					P	HPO:skoehler[2013-05-07]
OMIM:606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS		HP:0002240	OMIM:606445	TAS					P	HPO:skoehler[2013-05-07]
OMIM:606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS		HP:0100827	OMIM:606445	IEA					P	HPO:skoehler[2018-10-08]
OMIM:606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS		HP:0001744	OMIM:606445	TAS					P	HPO:skoehler[2013-05-07]
OMIM:606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS		HP:0000006	OMIM:606445	TAS					I	HPO:skoehler[2013-05-07]
OMIM:619565	Dystonia 31		HP:0003621	PMID:34596301	PCS		2/5			C	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0002356	PMID:34596301	PCS		5/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0002015	PMID:34596301	PCS		1/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0001300	PMID:34596301	PCS		2/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0003552	PMID:34596301	PCS		1/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0001288	PMID:34596301	PCS		3/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0031959	PMID:34596301	PCS		4/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0031960	PMID:34596301	PCS		5/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0012179	PMID:34596301	PCS		2/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0000716	PMID:34596301	PCS		1/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0011462	PMID:34596301	PCS		3/5			C	HPO:probinson[2022-02-04];HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0000007	PMID:34596301	PCS					I	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0007325	PMID:34596301	PCS		3/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0001621	PMID:34596301	PCS		3/5			P	HPO:probinson[2022-02-04]
OMIM:619565	Dystonia 31		HP:0002533	PMID:34596301	PCS					P	HPO:probinson[2022-02-04]
OMIM:230300	GALACTORRHEA		HP:0000007	OMIM:230300	IEA					I	HPO:iea[2009-02-17]
OMIM:230300	GALACTORRHEA		HP:0100829	OMIM:230300	IEA					P	HPO:skoehler[2015-01-21]
OMIM:230300	GALACTORRHEA		HP:0000119	OMIM:230300	IEA					P	HPO:iea[2009-02-17]
OMIM:230300	GALACTORRHEA		HP:0000765	OMIM:230300	IEA					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0002542	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0002015	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0001310	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0002310	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0003487	OMIM:164500	IEA					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0001260	PMID:19659750	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000580	OMIM:164500	TAS					P	HPO:probinson[2017-12-22]
OMIM:164500	Spinocerebellar ataxia 7		HP:0002072	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0002073	PMID:19659750	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0002071	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000529	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000639	PMID:19659750	PCS		2/2			P	HPO:iea[2010-09-13]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000608	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000514	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000623	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000648	PMID:19659750	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0001257	OMIM:164500	TAS					P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0001268	PMID:9781533	PCS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0000006	OMIM:164500	TAS					I	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0001337	PMID:19659750	PCS		2/2			P	HPO:iea[2010-09-13]
OMIM:164500	Spinocerebellar ataxia 7		HP:0001347	OMIM:164500	PCS		7/7			P	HPO:iea[2009-02-17]
OMIM:164500	Spinocerebellar ataxia 7		HP:0003744	OMIM:164500	TAS					I	HPO:iea[2009-02-17]
OMIM:113950	Bundle branch block, familial isolated complete right		HP:0011712	OMIM:113950	TAS					P	HPO:skoehler[2012-11-16]
OMIM:113950	Bundle branch block, familial isolated complete right		HP:0001626	OMIM:113950	IEA					P	HPO:iea[2009-02-17]
OMIM:113950	Bundle branch block, familial isolated complete right		HP:0000006	OMIM:113950	IEA					I	HPO:iea[2009-02-17]
OMIM:136520	Foveal hypoplasia and presenile cataract syndromefoveal hypoplasia, isolated, included		HP:0006934	OMIM:136520	IEA					P	HPO:iea[2009-02-17]
OMIM:136520	Foveal hypoplasia and presenile cataract syndromefoveal hypoplasia, isolated, included		HP:0007819	OMIM:136520	IEA					P	HPO:iea[2009-02-17]
OMIM:136520	Foveal hypoplasia and presenile cataract syndromefoveal hypoplasia, isolated, included		HP:0007750	OMIM:136520	IEA					P	HPO:iea[2009-02-17]
OMIM:136520	Foveal hypoplasia and presenile cataract syndromefoveal hypoplasia, isolated, included		HP:0000505	OMIM:136520	IEA					P	HPO:iea[2009-02-17]
OMIM:136520	Foveal hypoplasia and presenile cataract syndromefoveal hypoplasia, isolated, included		HP:0000006	OMIM:136520	IEA					I	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000220	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0001792	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0002287	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000365	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0004322	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000160	PMID:12766194	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000460	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0030056	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0001092	PMID:12766194	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0045075	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0008070	OMIM:129400	PCS		20/20			P	HPO:skoehler[2013-06-11];HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0001805	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000958	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0006297	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0005709	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000679	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0007500	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000059	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000653	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0002217	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0002558	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0200141	OMIM:129400	TAS					P	HPO:skoehler[2013-08-18]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000698	OMIM:129400	TAS					P	HPO:skoehler[2013-06-13]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0002235	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0002213	OMIM:129400	PCS					P	HPO:iea[2012-03-01]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000175	PMID:12766194	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000670	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000430	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000193	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000691	OMIM:129400	TAS					P	HPO:skoehler[2013-08-10]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0005280	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000508	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000327	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000668	PMID:12766194	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000403	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000348	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0007476	OMIM:129400	IEA					P	HPO:skoehler[2015-01-14]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000966	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0001159	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0008404	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000047	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000982	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000963	OMIM:129400	IEA					P	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000204	PMID:12766194	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-05]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000006	OMIM:129400	IEA					I	HPO:iea[2009-02-17]
OMIM:129400	Rapp-Hodgkin syndrome		HP:0000402	PMID:12766194	PCS		1/1			P	HPO:probinson[2022-11-05]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0003422	PMID:15214000	TAS					P	HPO:probinson[2013-03-25]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0003521	OMIM:608681	TAS					P	HPO:probinson[2015-02-21]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0000902	PMID:15214000	PCS					P	HPO:probinson[2013-03-25]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0002937	OMIM:608681	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0000470	OMIM:608681	TAS					P	HPO:probinson[2013-03-25]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0000007	OMIM:608681	TAS					I	HPO:probinson[2013-01-09]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0002205	OMIM:608681	TAS					P	HPO:probinson[2015-02-21]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0002091	OMIM:608681	TAS		44%			P	HPO:probinson[2013-03-25]
OMIM:608681	Spondylocostal dysostosis 2, autosomal recessive		HP:0008428	OMIM:608681	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001331	PMID:31079899	PCS		1/3			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000582	PMID:31079899	PCS		3/3			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000340	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0002540	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000463	PMID:31079899	PCS		3/3			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0004322	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0002365	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001250	PMID:31079899	PCS		2/2			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001274	PMID:31079899	PCS		1/3			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0003593	OMIM:618492	IEA					C	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001290	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001270	PMID:31079899	PCS		5/5			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000718	PMID:31079899	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000414	PMID:31079899	PCS		3/3			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001347	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000252	PMID:31079899	PCS	HP:0003577	5/5			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0002059	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000750	PMID:31079899	PCS		5/5			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0002079	PMID:31079899	PCS		1/3			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0031936	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001260	PMID:31079899	PCS		3/3			P	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001263	PMID:31079899	PCS		5/5			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0011344	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000448	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000007	PMID:31079899	PCS					I	HPO:probinson[2019-07-07];HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0007018	PMID:31079899	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0000520	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001257	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0009879	PMID:31079899	PCS		3/3			P	HPO:probinson[2019-07-07]
OMIM:618492	Neurodevelopmental disorder with microcephaly and structural brain anomalies		HP:0001611	OMIM:618492	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300758	Hypospadias 2, X-linked		HP:0000808	PMID:17086185	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:300758	Hypospadias 2, X-linked		HP:0003577	PMID:17086185	PCS		4/4			C	HPO:probinson[2023-02-20]
OMIM:300758	Hypospadias 2, X-linked		HP:0001419	PMID:17086185	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-20]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000684	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000365	PMID:16835913	PCS		3/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000365	PMID:16835913	PCS		6/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0100490	PMID:16835913	PCS		8/9	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0100490	PMID:16835913	PCS		9/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000280	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0008097	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000316	PMID:16835913	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006155	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001648	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002857	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0009702	PMID:16835913	PCS		1/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0009702	PMID:16835913	PCS		0/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001007	OMIM:305620	TAS					P	HPO:probinson[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001249	OMIM:305620;PMID:16835913	PCS		10/30			P	HPO:probinson[2022-08-24];HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0003202	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000175	PMID:16835913	PCS		1/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000175	PMID:16835913	PCS		0/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000494	PMID:16835913	PCS		9/9	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000494	PMID:16835913	PCS		7/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001220	PMID:16835913	PCS		8/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001220	PMID:16835913	PCS		10/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002673	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000331	OMIM:305620	TAS					P	HPO:probinson[2012-04-30]
OMIM:305620	Frontometaphyseal dysplasia		HP:0003083	PMID:16835913	PCS		4/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0003083	PMID:16835913	PCS		1/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006380	OMIM:305620	TAS					P	HPO:probinson[2012-05-27]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000407	OMIM:305620	IEA					P	HPO:skoehler[2010-06-20]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001419	PMID:12612583	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002949	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0004608	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000689	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006466	OMIM:305620	TAS					P	HPO:probinson[2012-05-27]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006665	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002700	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002987	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0004602	PMID:16835913	PCS		0/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0004602	PMID:16835913	PCS		3/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000126	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006207	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0010307	OMIM:305620	IEA					P	HPO:skoehler[2010-06-20]
OMIM:305620	Frontometaphyseal dysplasia		HP:0003691	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001592	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0009004	PMID:16835913	PCS		9/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0009004	PMID:16835913	PCS		11/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000218	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0009768	OMIM:305620	TAS					P	HPO:probinson[2012-06-10]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006335	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000336	PMID:16835913	PCS		9/9	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000336	PMID:16835913	PCS		10/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000336	PMID:16835913	PCS		11/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000336	PMID:16835913	PCS		9/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002996	PMID:16835913	PCS		9/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002996	PMID:16835913	PCS		5/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001166	PMID:16835913	PCS		8/9	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001166	PMID:16835913	PCS		5/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001363	PMID:16835913	PCS		1/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001363	PMID:16835913	PCS		0/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002650	PMID:16835913	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002650	PMID:16835913	PCS		2/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000431	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000072	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006440	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001833	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001239	OMIM:305620	TAS					P	HPO:probinson[2012-05-27]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006487	PMID:16835913	PCS		5/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0006487	PMID:16835913	PCS		2/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0000307	OMIM:305620	TAS					P	HPO:probinson[2012-04-30]
OMIM:305620	Frontometaphyseal dysplasia		HP:0003779	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0001634	OMIM:305620	IEA					P	HPO:iea[2009-02-17]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002688	PMID:16835913	PCS		8/9	MALE		P	HPO:probinson[2022-08-24]
OMIM:305620	Frontometaphyseal dysplasia		HP:0002688	PMID:16835913	PCS		6/11	FEMALE		P	HPO:probinson[2022-08-24]
OMIM:120430	Coloboma of optic nerveoptic nerve head pits, bilateral congenital, included		HP:0000541	OMIM:120430	IEA					P	HPO:iea[2009-02-17]
OMIM:120430	Coloboma of optic nerveoptic nerve head pits, bilateral congenital, included		HP:0000006	OMIM:120430	IEA					I	HPO:iea[2009-02-17]
OMIM:120430	Coloboma of optic nerveoptic nerve head pits, bilateral congenital, included		HP:0000588	OMIM:120430	IEA					P	HPO:iea[2009-02-17]
OMIM:253300	Spinal muscular atrophy, type I		HP:0002421	PMID:19780763	PCS					P	HPO:probinson[2022-03-16]
OMIM:253300	Spinal muscular atrophy, type I		HP:0003445	OMIM:253300	IEA					P	HPO:iea[2009-02-17]
OMIM:253300	Spinal muscular atrophy, type I		HP:0001284	OMIM:253300	IEA					P	HPO:iea[2009-02-17]
OMIM:253300	Spinal muscular atrophy, type I		HP:0003593	PMID:19780763	PCS		50/66			C	HPO:probinson[2022-03-16];HPO:probinson[2022-03-16]
OMIM:253300	Spinal muscular atrophy, type I		HP:0001290	PMID:19780763	PCS					P	HPO:probinson[2022-03-16]
OMIM:253300	Spinal muscular atrophy, type I		HP:0002093	OMIM:253300	IEA					P	HPO:iea[2009-02-17]
OMIM:253300	Spinal muscular atrophy, type I		HP:0001629	OMIM:253300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:253300	Spinal muscular atrophy, type I		HP:0003819	PMID:19780763	PCS					C	HPO:probinson[2022-03-16]
OMIM:253300	Spinal muscular atrophy, type I		HP:0000007	PMID:19780763	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:253300	Spinal muscular atrophy, type I		HP:0001558	PMID:19780763	PCS	HP:0011461	22/66			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-16]
OMIM:253300	Spinal muscular atrophy, type I		HP:0001308	OMIM:253300	TAS					P	HPO:probinson[2012-04-27]
OMIM:253300	Spinal muscular atrophy, type I		HP:0002878	OMIM:253300	TAS					P	HPO:skoehler[2014-06-24]
OMIM:253300	Spinal muscular atrophy, type I		HP:0007126	OMIM:253300	TAS					P	HPO:probinson[2012-04-27]
OMIM:253300	Spinal muscular atrophy, type I		HP:0007269	PMID:19780763	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-16]
OMIM:253300	Spinal muscular atrophy, type I		HP:0002205	OMIM:253300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253300	Spinal muscular atrophy, type I		HP:0001631	OMIM:253300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:253300	Spinal muscular atrophy, type I		HP:0003623	PMID:19780763	PCS		16/66			C	HPO:probinson[2022-03-16]
OMIM:601869	Deafness, autosomal recessive 15		HP:0001751	PMID:21660509	PCS		0/17			P	HP:probinson[2019-03-09];HPO:probinson[2024-03-10]
OMIM:601869	Deafness, autosomal recessive 15		HP:0000407	PMID:21660509	PCS		17/17			P	HP:probinson[2019-03-09]
OMIM:601869	Deafness, autosomal recessive 15		HP:0000007	PMID:21326233	PCS					I	HPO:skoehler[2012-10-16];HP:probinson[2019-03-09]
OMIM:601869	Deafness, autosomal recessive 15		HP:0000505	PMID:21660509	PCS		0/17			P	HP:probinson[2019-03-09];HPO:probinson[2024-03-10]
OMIM:601869	Deafness, autosomal recessive 15		HP:0000399	PMID:21326233	PCS		2/2			P	HP:probinson[2019-03-09]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000286	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0030799	OMIM:200980	TAS					P	HPO:skoehler[2017-07-13]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001770	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000882	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0002089	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000189	OMIM:200980	TAS					P	HPO:skoehler[2013-08-18]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0002561	OMIM:200980	TAS					P	HPO:skoehler[2015-01-04]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001171	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001829	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0002937	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0031909	OMIM:200980	IEA					P	HPO:skoehler[2018-10-08]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000813	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000218	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001626	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000774	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000113	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000358	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000776	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001562	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0002751	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000494	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0003762	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0003022	OMIM:200980	TAS					P	HPO:probinson[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001161	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0010477	OMIM:200980	TAS					P	HPO:skoehler[2017-07-13]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0006381	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0002827	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001839	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000921	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000007	OMIM:200980	IEA					I	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000769	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0008468	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000268	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0001511	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0003316	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000069	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000883	OMIM:200980	IEA					P	HPO:skoehler[2010-06-20]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0002987	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000369	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0002984	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000347	OMIM:200980	TAS				HP:0012828	P	HPO:probinson[2012-04-30]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0000104	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:200980	Acrorenal-Mandibular syndrome		HP:0006426	OMIM:200980	IEA					P	HPO:iea[2009-02-17]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0003774	PMID:7493166;PMID:10198255	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0003233	PMID:10487826	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0001399	PMID:8675681	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0003596	PMID:10487826;PMID:8675681;PMID:9916936	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0012309	PMID:9916936	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0003155	PMID:7493166	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0002240	PMID:7493166	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0001609	PMID:12050338	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0011462	PMID:12050338;PMID:7493166;PMID:10198255;PMID:3142462	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0000978	PMID:3142462	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0000956	PMID:10198255	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0030843	PMID:8675681;PMID:9916936;PMID:10198255	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0002014	PMID:7493166	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0001640	PMID:9916936	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0010637	PMID:9916936	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0002094	PMID:10487826	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0000093	PMID:7493166	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0031799	PMID:10487826	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0011034	PMID:10487826	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0002907	PMID:7493166	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0001917	PMID:8675681;PMID:12050338;PMID:7493166	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0000822	PMID:3142462	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0000789	PMID:12050338	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0001635	PMID:10487826;PMID:9916936;PMID:10198255	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0012280	PMID:8675681;PMID:7493166;PMID:3142462	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0001638	PMID:9916936;PMID:7493166;PMID:10198255	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0001873	PMID:3142462	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0004944	PMID:10198255	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0000006	PMID:3142462	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620657	Amyloidosis, hereditary systemic 3		HP:0003216	PMID:10198255	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:150699	Leiomyoma, uterine		HP:0000131	PMID:21868628	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:150699	Leiomyoma, uterine		HP:0001442	PMID:21868628	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:150699	Leiomyoma, uterine		HP:0003581	PMID:21868628	PCS					C	HPO:probinson[2023-02-04]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0001276	PMID:25205402;PMID:20635338	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18];HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000286	PMID:23332918;PMID:25205402;PMID:20635338	PCS		8/24			P	HPO:probinson[2022-04-11];HPO:probinson[2022-06-18];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000582	PMID:23332918;PMID:25205402	PCS		4/23			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000486	PMID:23332918;PMID:25205402	PCS		6/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000463	PMID:23332918;PMID:25205402	PCS		3/23			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000023	PMID:23332918	PCS		1/21			P	HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0004322	PMID:23332918;PMID:25205402	PCS		13/22			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0002002	PMID:20635338	PCS		1/1			P	HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000160	PMID:23332918;PMID:25205402	PCS		12/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0003593	PMID:25205402;PMID:20635338	PCS		4/5			C	HPO:probinson[2022-04-11];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0001290	PMID:23332918	PCS		8/21			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0005274	PMID:23332918;PMID:25205402	PCS		7/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0012745	PMID:23332918;PMID:25205402	PCS		9/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0010862	PMID:20635338	PCS		1/1			P	HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0012471	PMID:25205402	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000316	PMID:23332918;PMID:25205402	PCS		10/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000752	PMID:23332918;PMID:25205402	PCS		4/23			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0001249	PMID:23332918;PMID:25205402	PCS		22/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0003623	PMID:25205402	PCS		1/2			C	HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000154	PMID:25205402	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0002553	PMID:23332918;PMID:25205402	PCS		9/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000494	PMID:25205402	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000252	PMID:23332918;PMID:25205402	PCS		16/22			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000750	PMID:25205402;PMID:20635338	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000574	PMID:25205402	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0002650	PMID:23332918;PMID:25205402	PCS		2/11			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000431	PMID:23332918;PMID:20635338	PCS		8/22			P	HPO:probinson[2022-04-11];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0011968	PMID:23332918;PMID:25205402	PCS		12/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0001263	PMID:23332918;PMID:25205402	PCS		22/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0025112	PMID:23332918;PMID:25205402	PCS		3/10			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0100021	PMID:23332918	PCS		9/21			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0005280	PMID:25205402	PCS		2/2			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0006184	PMID:25205402	PCS		2/2			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0002808	PMID:23332918	PCS		2/9			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0001518	PMID:23332918	PCS		7/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000729	PMID:23332918;PMID:25205402;PMID:20635338	PCS		10/24			P	HPO:probinson[2022-04-11];HPO:probinson[2022-06-18];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000508	PMID:23332918;PMID:25205402	PCS		10/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0001537	PMID:23332918	PCS		1/21			P	HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0002804	PMID:23332918	PCS	HP:0003577	3/20			P	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0002804	PMID:25205402	PCS		2/2			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0004209	PMID:20635338	PCS		1/1			P	HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0001511	PMID:25205402	PCS		1/2			P	HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000520	PMID:23332918;PMID:25205402	PCS		7/23			P	HPO:probinson[2022-04-11];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000322	PMID:23332918;PMID:25205402	PCS		10/23			P	HPO:probinson[2022-04-11];HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000248	PMID:25205402	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000006	PMID:23332918	PCS					I	HPO:skoehler[2015-09-14];HPO:probinson[2022-04-11]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000369	PMID:23332918;PMID:25205402;PMID:20635338	PCS		8/23			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11];HPO:probinson[2022-06-18]
OMIM:615834	Intellectual developmental disorder, autosomal dominant 26		HP:0000347	PMID:23332918;PMID:25205402;PMID:20635338	PCS		9/24			P	HPO:probinson[2022-04-11];HPO:probinson[2022-06-18];HPO:probinson[2022-04-11];HPO:probinson[2022-04-11]
OMIM:602390	Hemochromatosis, type 2A		HP:0000044	PMID:14982867	PCS		6/7			P	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0001254	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0003452	PMID:14982867	PCS		7/7			P	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0000141	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0002240	PMID:14982867	PCS		7/7			P	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0001394	PMID:14982867	PCS		2/4			P	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0011675	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0003281	PMID:14982867	PCS		4/4			P	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0011462	PMID:14982867	PCS					C	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0000789	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0000007	PMID:14982867	PCS					I	HPO:probinson[2013-01-09]
OMIM:602390	Hemochromatosis, type 2A		HP:0000953	PMID:14982867	PCS					P	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0001635	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0001638	PMID:14982867	PCS		2/7			P	HPO:probinson[2013-02-18]
OMIM:602390	Hemochromatosis, type 2A		HP:0001744	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0001644	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0000027	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602390	Hemochromatosis, type 2A		HP:0001369	OMIM:602390	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001671	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0003577	PMID:20921022	PCS		5/5			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0010804	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001651	OMIM:614294	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000023	PMID:20921022	PCS		1/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0004322	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001629	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000316	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0100807	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001748	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000752	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000776	PMID:20921022	PCS		3/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000358	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0002058	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0005469	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000175	PMID:20921022	PCS		1/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000494	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000233	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0002079	PMID:20921022	PCS		1/3			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001263	PMID:20921022	PCS		2/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000470	PMID:20921022	PCS		2/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0100581	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0011641	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000767	PMID:20921022	PCS		1/5			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000664	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001511	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0007018	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001510	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0001972	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000465	PMID:20921022	PCS		2/5			P	HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000006	PMID:20921022	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000204	OMIM:614294	TAS					P	HPO:skoehler[2015-06-22]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000028	PMID:20921022	PCS		2/3			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-09-26]
OMIM:614294	Chromosome 15q25 deletion syndrome		HP:0000369	PMID:20921022	PCS		1/5			P	HPO:probinson[2022-09-26]
OMIM:616483	Infantile liver failure syndrome 2		HP:0001254	PMID:26073778	PCS					P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0002013	PMID:26073778	PCS					P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0001250	PMID:26073778	PCS		1/10			P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0003593	PMID:26073778	PCS					C	HPO:probinson[2020-09-13]
OMIM:616483	Infantile liver failure syndrome 2		HP:0002480	PMID:26073778	PCS					P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0008151	PMID:26073778	PCS				HP:0025215	P	HPO:probinson[2020-09-13]
OMIM:616483	Infantile liver failure syndrome 2		HP:0000007	PMID:26073778	PCS					I	HPO:skoehler[2017-07-13]
OMIM:616483	Infantile liver failure syndrome 2		HP:0001987	PMID:26073778	PCS					P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0001943	PMID:26073778	PCS					P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0001638	PMID:26073778	PCS		1/10			P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0006554	PMID:26073778	PCS	HP:0003593				P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0002910	PMID:26073778	PCS					P	HPO:nvasilevsky[2018-04-05]
OMIM:616483	Infantile liver failure syndrome 2		HP:0000952	PMID:26073778	PCS					P	HPO:nvasilevsky[2018-04-05]
OMIM:606690	LYMPHANGIOLEIOMYOMATOSIS		HP:0001442	OMIM:606690	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:606690	LYMPHANGIOLEIOMYOMATOSIS		HP:0012798	OMIM:606690	IEA					P	HPO:skoehler[2015-01-27]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0002153	PMID:8589714	PCS					P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0000848	PMID:8589714	PCS					P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0000859	PMID:8589714	PCS					P	HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0001944	PMID:8589714	PCS					P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0002902	PMID:8589714	PCS					P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0000007	PMID:8589714	PCS					I	HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0002615	PMID:8589714	PCS					P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0001942	PMID:8589714	PCS					P	HPO:probinson[2023-03-04];HPO:probinson[2023-03-04]
OMIM:620125	Pseudohypoaldosteronism, type IB2, autosomal recessive		HP:0003623	PMID:8589714	PCS					C	HPO:probinson[2023-03-04]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0006517	PMID:18955570	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-10-13]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0001508	PMID:18955570	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0032341	PMID:18955570	PCS	HP:0003621	1/2			P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0025179	PMID:18955570	PCS	HP:0003621	2/2			P	HPO:probinson[2020-10-13]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0032342	PMID:18955570	PCS	HP:0003621	1/2			P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0001417	PMID:18955570	PCS					I	HPO:probinson[2013-03-23]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0002789	PMID:18955570	PCS					P	HPO:probinson[2013-01-09]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0002091	PMID:18955570	PCS				HP:0012828	P	HPO:probinson[2013-03-23]
OMIM:300770	Surfactant metabolism dysfunction, pulmonary, 4		HP:0045051	PMID:18955570	PCS	HP:0003621	1/1			P	HPO:probinson[2020-10-13]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0003510	PMID:29576217	PCS		1/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0003676	PMID:29576217	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0010528	PMID:29576217	PCS		1/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000540	PMID:29576217	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001332	PMID:29576217	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001250	PMID:29576217	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001272	PMID:29576217	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001251	PMID:29576217	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0003593	PMID:29576217	PCS		2/4			C	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001270	PMID:29576217	PCS		1/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002080	PMID:29576217	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000639	PMID:29576217	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001508	PMID:29576217	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0011463	PMID:29576217	PCS		1/4			C	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0003429	PMID:29576217	PCS		4/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002415	PMID:29576217	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000572	PMID:29576217	PCS		1/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000252	PMID:29576217	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002015	PMID:29576217	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002059	PMID:29576217	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0003621	PMID:29576217	PCS		1/4			C	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002079	PMID:29576217	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002376	PMID:29576217	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0011968	PMID:29576217	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001260	PMID:29576217	PCS		2/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001263	PMID:29576217	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0033454	PMID:29576217	PCS		1/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000529	OMIM:617951	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000407	PMID:29576217	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0033044	PMID:29576217	PCS		3/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0034332	PMID:29576217	PCS		4/4			P	HPO:probinson[2022-09-05]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000646	PMID:29576217	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000007	PMID:29576217	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0007256	PMID:29576217	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0000648	PMID:29576217	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002505	PMID:29576217	PCS		1/4			P	HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0001257	PMID:29576217	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:617951	Leukodystrophy, hypomyelinating, 15		HP:0002305	PMID:29576217	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-05-26]
OMIM:255995	Congenital myopathy 13		HP:0002047	OMIM:255995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255995	Congenital myopathy 13		HP:0003577	PMID:28411587;PMID:23736855	PCS		2/2			C	HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0005775	OMIM:255995	IEA					P	HPO:iea[2009-02-17]
OMIM:255995	Congenital myopathy 13		HP:0004322	OMIM:255995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255995	Congenital myopathy 13		HP:0001371	OMIM:255995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255995	Congenital myopathy 13		HP:0000581	OMIM:255995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255995	Congenital myopathy 13		HP:0001252	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0012745	OMIM:255995	TAS					P	HPO:skoehler[2014-03-24]
OMIM:255995	Congenital myopathy 13		HP:0012548	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0001270	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0003391	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0030319	PMID:28411587	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0002119	OMIM:255995	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:255995	Congenital myopathy 13		HP:0002714	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0000218	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0001324	PMID:28411587	PCS	HP:0003577	1/1			P	HPO:skoehler[2015-01-04]
OMIM:255995	Congenital myopathy 13		HP:0003701	PMID:28411587	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0001249	OMIM:255995	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:255995	Congenital myopathy 13		HP:0001265	OMIM:255995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255995	Congenital myopathy 13		HP:0002751	OMIM:255995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255995	Congenital myopathy 13		HP:0002058	OMIM:255995	IEA					P	HPO:iea[2009-02-17]
OMIM:255995	Congenital myopathy 13		HP:0003202	OMIM:255995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255995	Congenital myopathy 13		HP:0000175	OMIM:255995	IEA					P	HPO:iea[2009-02-17]
OMIM:255995	Congenital myopathy 13		HP:0000494	OMIM:255995	TAS					P	HPO:skoehler[2012-11-20]
OMIM:255995	Congenital myopathy 13		HP:0000252	OMIM:255995	IEA					P	HPO:skoehler[2019-02-22]
OMIM:255995	Congenital myopathy 13		HP:0002650	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0011968	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:probinson[2023-07-03];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:255995	Congenital myopathy 13		HP:0001284	PMID:28411587	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0012416	PMID:28411587	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0011800	OMIM:255995	IEA					P	HPO:skoehler[2019-02-22]
OMIM:255995	Congenital myopathy 13		HP:0012418	PMID:28411587	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0002091	OMIM:255995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255995	Congenital myopathy 13		HP:0000506	OMIM:255995	TAS					P	HPO:skoehler[2012-10-17]
OMIM:255995	Congenital myopathy 13		HP:0012240	PMID:28411587	PCS		1/1			P	HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0000508	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0000007	PMID:23736855	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-21]
OMIM:255995	Congenital myopathy 13		HP:0000405	OMIM:255995	IEA					P	HPO:skoehler[2019-02-22]
OMIM:255995	Congenital myopathy 13		HP:0000248	OMIM:255995	IEA					P	HPO:skoehler[2019-02-22]
OMIM:255995	Congenital myopathy 13		HP:0000028	OMIM:255995	IEA					P	HPO:skoehler[2010-06-18]
OMIM:255995	Congenital myopathy 13		HP:0000369	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:255995	Congenital myopathy 13		HP:0000347	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:probinson[2023-07-03];HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:255995	Congenital myopathy 13		HP:0001776	PMID:28411587;PMID:23736855	PCS		2/2			P	HPO:probinson[2023-02-21];HPO:probinson[2023-07-03]
OMIM:165150	Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency		HP:0000221	OMIM:165150	IEA					P	HPO:iea[2009-02-17]
OMIM:165150	Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency		HP:0007650	OMIM:165150	IEA					P	HPO:iea[2009-02-17]
OMIM:165150	Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency		HP:0000006	OMIM:165150	IEA					I	HPO:iea[2009-02-17]
OMIM:165150	Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency		HP:0001249	OMIM:165150	IEA					P	HPO:iea[2009-02-17]
OMIM:614280	Epilepsy, juvenile myoclonic, susceptibility to, 9		HP:0002373	OMIM:614280	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614280	Epilepsy, juvenile myoclonic, susceptibility to, 9		HP:0002121	OMIM:614280	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614280	Epilepsy, juvenile myoclonic, susceptibility to, 9		HP:0000006	OMIM:614280	TAS					I	HPO:skoehler[2012-10-17]
OMIM:604093	Keratosis pilaris atrophicans		HP:0009926	PMID:26142438	PCS	HP:0003593				P	HPO:lccarmody[2018-10-03]
OMIM:604093	Keratosis pilaris atrophicans		HP:0000561	PMID:26142438	PCS	HP:0011463	4/4			P	HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-10]
OMIM:604093	Keratosis pilaris atrophicans		HP:0032152	PMID:26142438	PCS		4/4			P	HPO:skoehler[2019-09-07]
OMIM:604093	Keratosis pilaris atrophicans		HP:0031285	PMID:26142438	PCS					P	HPO:lccarmody[2018-10-03]
OMIM:604093	Keratosis pilaris atrophicans		HP:0003593	PMID:26142438	PCS		4/4			C	HPO:probinson[2024-03-10]
OMIM:604093	Keratosis pilaris atrophicans		HP:0000007	PMID:26142438	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-10]
OMIM:604093	Keratosis pilaris atrophicans		HP:0025249	PMID:26142438	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-10]
OMIM:604093	Keratosis pilaris atrophicans		HP:0200034	PMID:26142438	PCS		4/4			P	HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-10]
OMIM:604093	Keratosis pilaris atrophicans		HP:0010783	PMID:26142438	PCS		4/4			P	HPO:lccarmody[2018-10-03]
OMIM:604093	Keratosis pilaris atrophicans		HP:0000504	PMID:26142438	PCS		0/4			P	HPO:lccarmody[2018-10-03];HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-10]
OMIM:604093	Keratosis pilaris atrophicans		HP:0045075	PMID:26142438	PCS	HP:0011463	4/4			P	HPO:lccarmody[2018-10-03];HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-10]
OMIM:604093	Keratosis pilaris atrophicans		HP:0001249	PMID:26142438	PCS		0/4			P	HPO:lccarmody[2018-10-03];HPO:lccarmody[2018-10-03];HPO:probinson[2024-03-10]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0003201	OMIM:188580	IEA					P	HPO:iea[2009-02-17]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0000836	OMIM:188580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0002900	OMIM:188580	IEA					P	HPO:iea[2009-02-17]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0001649	OMIM:188580	IEA					P	HPO:skoehler[2018-10-08]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0001824	OMIM:188580	IEA					P	HPO:skoehler[2019-09-07]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0001324	OMIM:188580	IEA					P	HPO:iea[2009-02-17]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0001962	OMIM:188580	TAS					P	HPO:skoehler[2013-06-23]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0003745	OMIM:188580	TAS					I	HPO:skoehler[2015-12-30]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0003768	OMIM:188580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0000853	OMIM:188580	TAS					P	HPO:skoehler[2013-06-23]
OMIM:188580	Thyrotoxic periodic paralysis, susceptibility to, 1		HP:0000006	OMIM:188580	IEA					I	HPO:skoehler[2019-04-18]
OMIM:116800	Cataract, lamellar		HP:0100018	OMIM:116800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:116800	Cataract, lamellar		HP:0001134	OMIM:116800	IEA					P	HPO:iea[2009-02-17]
OMIM:116800	Cataract, lamellar		HP:0010693	OMIM:116800	TAS					P	HPO:skoehler[2012-11-25]
OMIM:116800	Cataract, lamellar		HP:0007971	PMID:12089525	PCS					P	HPO:skoehler[2010-06-18]
OMIM:116800	Cataract, lamellar		HP:0000006	PMID:12089525	PCS					I	HPO:iea[2009-02-17]
OMIM:116800	Cataract, lamellar		HP:0010920	OMIM:116800	TAS					P	HPO:probinson[2012-07-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0007418	OMIM:212360	TAS	HP:0003577				P	HPO:probinson[2013-12-18]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0001041	OMIM:212360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0002164	OMIM:212360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0100490	OMIM:212360	TAS					P	HPO:probinson[2013-12-18]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0011838	OMIM:212360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0000958	OMIM:212360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0032152	OMIM:212360	IEA					P	HPO:skoehler[2019-02-22]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0000519	OMIM:212360	IEA					P	HPO:iea[2009-02-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0009775	OMIM:212360	IEA					P	HPO:iea[2009-02-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0000007	OMIM:212360	IEA					I	HPO:iea[2009-02-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0000972	OMIM:212360	TAS					P	HPO:skoehler[2012-10-17]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0008404	OMIM:212360	TAS					P	HPO:skoehler[2013-05-03]
OMIM:212360	Palmoplantar keratoderma and congenital alopecia 2		HP:0000962	OMIM:212360	IEA					P	HPO:iea[2009-02-17]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0001363	OMIM:600593	IEA					P	HPO:iea[2009-02-17]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0005776	OMIM:600593	TAS					P	HPO:probinson[2009-02-17]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0010164	OMIM:600593	TAS					P	HPO:probinson[2012-06-11]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0010230	OMIM:600593	TAS					P	HPO:probinson[2012-06-11]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0006110	OMIM:600593	TAS					P	HPO:probinson[2012-06-09]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0001822	OMIM:600593	IEA					P	HPO:iea[2009-02-17]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0000006	OMIM:600593	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:600593	Craniosynostosis, Adelaide type		HP:0006118	OMIM:600593	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0000175	PMID:12219090	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0008726	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0003577	PMID:20803643	PCS		6/6			C	HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0000013	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0000046	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0001762	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0003298	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0000193	PMID:20803643	PCS		2/6			P	HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0000196	PMID:12219090	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0010554	PMID:12219090	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0000726	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0009755	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0009754	PMID:12219090	PCS		2/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0000048	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0000059	PMID:20803643	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0009757	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0009756	PMID:12219090	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0000006	PMID:12219090	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0000204	PMID:12219090	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119500	Popliteal pterygium syndrome		HP:0000028	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:119500	Popliteal pterygium syndrome		HP:0009758	OMIM:119500	IEA					P	HPO:iea[2009-02-17]
OMIM:617004	Polycystic liver disease 2		HP:0003581	PMID:15133510	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:617004	Polycystic liver disease 2		HP:0002240	PMID:15133510	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:617004	Polycystic liver disease 2		HP:0001407	PMID:15133510	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:617004	Polycystic liver disease 2		HP:0000006	PMID:15133510	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-06]
OMIM:601666	Diabetes mellitus, insulin-dependent, 15		HP:0000819	OMIM:601666	IEA					P	HPO:iea[2009-02-17]
OMIM:601666	Diabetes mellitus, insulin-dependent, 15		HP:0100651	OMIM:601666	TAS					P	HPO:skoehler[2012-10-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001770	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000365	PMID:22541558	PCS		19/20			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001377	PMID:22541558	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000486	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0004322	PMID:22541558	PCS		2/2			P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000122	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001172	PMID:22541558	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001849	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001607	PMID:22541558	PCS		1/9			P	HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0010055	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001845	OMIM:154400	TAS					P	HPO:skoehler[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000238	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0009466	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001643	OMIM:154400	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000278	OMIM:154400	TAS					P	HPO:skoehler[2015-04-05]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0007646	PMID:22541558	PCS		6/14			P	HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001249	PMID:22541558	PCS		1/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000358	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0002974	PMID:22541558	PCS		14/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000891	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000175	PMID:22541558	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000494	PMID:22541558	PCS		20/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000252	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000211	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001025	OMIM:154400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001263	PMID:22541558	PCS		3/11			P	HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0004692	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0011800	PMID:22541558	PCS		17/17			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0012385	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0002827	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0009777	PMID:22541558	PCS		7/22			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0009656	PMID:22541558	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0003319	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000405	PMID:22541558	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0007678	PMID:22541558	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0009778	PMID:22541558	PCS		5/20			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000006	PMID:22541558	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000204	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0002984	PMID:22541558	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000369	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000402	PMID:22541558	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000324	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0008749	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001199	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000220	PMID:22541558	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0003577	PMID:22541558	PCS		9/9			C	HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000384	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0010109	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000185	PMID:22541558	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0010034	PMID:22541558	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001629	PMID:22541558	PCS		2/9			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-11-08];HPO:probinson[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001822	PMID:22541558	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0009601	OMIM:154400	IEA					P	HPO:skoehler[2010-06-18]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000813	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0030084	OMIM:154400	TAS					P	HPO:skoehler[2014-09-21]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000378	PMID:22541558	PCS		3/13			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000377	PMID:22541558	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0004977	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001543	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000652	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000413	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000776	PMID:22541558	PCS		1/9			P	HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0006657	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0005349	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001622	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0002410	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000154	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000750	PMID:22541558	PCS		2/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0002650	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001762	PMID:22541558	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0002251	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000272	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0012478	PMID:22541558	PCS		2/4			P	HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000426	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001636	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0009554	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0009237	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0007776	PMID:22541558	PCS		5/14			P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0003974	PMID:22541558	PCS		1/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0000347	PMID:22541558	PCS		23/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-08]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001634	PMID:22541558	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0002126	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:154400	Acrofacial dysostosis 1, Nager type		HP:0001831	OMIM:154400	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0001773	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000365	OMIM:227330	TAS		HP:0040283			P	HPO:skoehler[2013-04-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000189	OMIM:227330	TAS					P	HPO:skoehler[2013-08-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000463	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0002002	OMIM:227330	IEA					P	HPO:skoehler[2010-06-20]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000023	OMIM:227330	TAS					P	HPO:skoehler[2013-04-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0003196	OMIM:227330	TAS					P	HPO:skoehler[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0008551	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000316	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0001547	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0003508	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000637	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000218	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0001169	OMIM:227330	IEA					P	HPO:skoehler[2010-06-20]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0200021	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0001840	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000358	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0001249	OMIM:227330	TAS		HP:0040283			P	HPO:skoehler[2013-04-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000154	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000472	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000494	OMIM:227330	TAS					P	HPO:skoehler[2013-04-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000211	OMIM:227330	TAS		HP:0040283			P	HPO:skoehler[2013-04-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0012385	OMIM:227330	TAS					P	HPO:skoehler[2013-10-22]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0002948	OMIM:227330	TAS		HP:0040283			P	HPO:skoehler[2013-04-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0100515	OMIM:227330	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000349	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000426	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000767	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000007	OMIM:227330	IEA					I	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000689	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0004209	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0005639	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0001159	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000248	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000325	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000028	OMIM:227330	TAS					P	HPO:skoehler[2013-04-18]
OMIM:227330	Faciodigitogenital syndrome, autosomal recessive		HP:0000049	OMIM:227330	IEA					P	HPO:iea[2009-02-17]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0001880	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0003203	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0410242	PMID:21524210	PCS		0/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0020086	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0002110	OMIM:226990	IEA					P	HPO:skoehler[2010-06-20]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0002240	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0003593	PMID:21524210	PCS		1/1			C	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0003073	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0012312	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0002090	OMIM:226990	IEA					P	HPO:skoehler[2010-06-20]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0012138	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0011897	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0001508	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0002719	OMIM:226990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0001903	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0000007	PMID:21524210	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0001945	PMID:21524210	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0002205	OMIM:226990	IEA					P	HPO:skoehler[2019-04-18]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0000246	OMIM:226990	IEA					P	HPO:skoehler[2010-06-20]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0002514	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0001873	PMID:21524210	PCS		1/1			P	HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0001744	PMID:21524210	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-11]
OMIM:226990	Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive		HP:0002721	PMID:21524210	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-11]
OMIM:300943	Pituitary adenoma 2, GH-secreting		HP:0002893	PMID:25470569	PCS					P	HPO:skoehler[2015-08-22]
OMIM:300943	Pituitary adenoma 2, GH-secreting		HP:0000845	PMID:25806920	PCS	HP:0003581				P	HPO:skoehler[2015-08-22]
OMIM:300943	Pituitary adenoma 2, GH-secreting		HP:0001417	PMID:25470569	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-08-09]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001276	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0002421	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0003676	PMID:30915432	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001332	OMIM:618451	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001250	OMIM:618451	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0003593	PMID:30915432	PCS		1/1			C	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0012448	OMIM:618451	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0000817	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001347	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0008936	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001344	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0002353	OMIM:618451	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0003487	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001266	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0002310	OMIM:618451	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0011968	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001263	OMIM:618451	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0002072	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0025190	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0100021	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0011800	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0012736	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0100660	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0012762	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0034295	PMID:30915432	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0000508	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0000007	PMID:30915432	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001935	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0000322	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001257	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0001931	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-05]
OMIM:618451	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia		HP:0000369	PMID:30915432	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0003676	PMID:26792856	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000340	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0001332	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0004322	PMID:26792856	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0003593	PMID:26792856	PCS		2/2			C	HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0004482	PMID:26792856	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000280	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0007281	PMID:26792856	PCS	HP:0003593	2/2			P	HPO:skoehler[2018-10-08]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000319	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0002415	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000179	PMID:26792856	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0008936	PMID:26792856	PCS		2/2			P	HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000011	PMID:26792856	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0002059	PMID:26792856	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000574	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0002376	PMID:26792856	PCS	HP:0003593	2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0002079	PMID:26792856	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0001284	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0034392	PMID:26792856	PCS		2/2			P	HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0034353	PMID:26792856	PCS		2/2			P	HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0009830	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000448	PMID:26792856	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000007	PMID:26792856	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000543	PMID:26792856	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-06-05]
OMIM:617762	Leukodystrophy, progressive, early childhood-onset		HP:0000369	PMID:26792856	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0003577	PMID:11919560	PCS		3/16			C	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0003596	PMID:11919560	PCS		2/16			C	HPO:probinson[2022-10-24];HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0002089	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0005576	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0030674	PMID:11919560	PCS		1/16			C	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0000083	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001395	PMID:11919560	PCS		13/16			P	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0002240	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0003593	PMID:11919560	PCS		4/16			C	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0002040	PMID:11919560	PCS		2/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001409	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0011463	PMID:11919560	PCS		1/16			C	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0011462	PMID:11919560	PCS		3/16			C	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0004719	PMID:11919560	PCS		9/16			P	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001944	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001405	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001407	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0000113	OMIM:263200	TAS					P	HPO:probinson[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001744	PMID:11919560	PCS		3/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0008659	PMID:11919560	PCS		1/16			P	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0003623	PMID:11919560	PCS		2/16			C	HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001562	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0005564	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0000822	PMID:11919560	PCS		12/16			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0000107	PMID:11919560	PCS		15/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0000007	PMID:11919560	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0001737	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0002009	OMIM:263200	IEA					P	HPO:iea[2009-02-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0003811	OMIM:263200	TAS		HP:0040283			C	HPO:probinson[2012-07-17]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0000105	PMID:11919560	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-24]
OMIM:263200	Polycystic kidney disease 4 with or without polycystic liver disease		HP:0002248	PMID:11919560	PCS		2/16			P	HPO:probinson[2022-10-24]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0003621	PMID:23716654	PCS		1/6			C	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0003596	PMID:23716654	PCS		1/6			C	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0000541	PMID:23716654	PCS		2/6			P	HPO:skoehler[2018-10-08]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0007917	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0001493	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0003593	PMID:23716654	PCS		1/6			C	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0100018	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0000518	PMID:23716654	PCS		1/6			P	HPO:skoehler[2015-08-02]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0000529	PMID:23716654	PCS					P	HPO:skoehler[2015-08-02];HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0011530	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0011463	PMID:23716654	PCS		1/6			C	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0007791	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0100019	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0020045	PMID:23716654	PCS		2/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0007663	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0030490	PMID:23716654	PCS		6/6			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0001489	PMID:23716654	PCS		1/6		HP:0003676	P	HPO:skoehler[2015-08-02]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0001147	PMID:23716654	PCS		1/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0000006	PMID:23716654	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0000666	PMID:23716654	PCS		2/6			P	HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0000545	PMID:23716654	PCS		2/6			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-04-19]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0000533	PMID:23716654	PCS		2/6			P	HPO:skoehler[2015-08-02]
OMIM:616468	Exudative vitreoretinopathy 6		HP:0003623	PMID:23716654	PCS		2/6			C	HPO:probinson[2023-04-19]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0010628	OMIM:611307	IEA					P	HPO:iea[2009-02-17]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003676	OMIM:611307	IEA					C	HPO:iea[2009-02-17]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003236	PMID:20096397	PCS		12/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-26];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003596	PMID:20096397	PCS		5/10			C	HPO:probinson[2023-02-26];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003560	PMID:20096397	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0009050	PMID:20096397	PCS		6/7			P	HPO:probinson[2023-02-26]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0009025	OMIM:611307	IEA					P	HPO:skoehler[2018-10-08];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0008981	PMID:20096397	PCS		4/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0011462	PMID:20096397	PCS		5/10			C	HPO:probinson[2023-02-26];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003749	PMID:20096397	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-26];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0000007	PMID:20096397	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-26]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003701	PMID:20096397	PCS		11/12			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-16]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003547	OMIM:611307	IEA					P	HPO:iea[2009-02-17]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003458	OMIM:611307	IEA					P	HPO:iea[2009-02-17]
OMIM:611307	Muscular dystrophy, limb-girdle, type 2L		HP:0003326	OMIM:611307	IEA					P	HPO:iea[2009-02-17]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0002487	PMID:32116545	PCS		8/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000486	PMID:32116545	PCS		4/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0004322	PMID:32116545	PCS		20/38			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001250	PMID:32116545	PCS		8/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001252	PMID:32116545	PCS		22/36			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000716	PMID:32116545	PCS		2/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000639	PMID:32116545	PCS		2/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000739	PMID:32116545	PCS		2/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0030043	PMID:32116545	PCS		2/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0002119	PMID:32116545	PCS		14/32			P	HPO:probinson[2020-08-02];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0030260	PMID:26166480	TAS		4/11			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001249	PMID:32116545	PCS		37/38			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001622	PMID:32116545	PCS		6/34			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000577	PMID:32116545	PCS		2/10			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001320	PMID:26166480	IEA		1/6			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000252	PMID:32116545	PCS		13/38			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0031418	OMIM:300957	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000750	PMID:32116545	PCS		31/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001288	PMID:32116545	PCS		18/38			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0011968	PMID:32116545	IEA		7/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001382	PMID:32116545	IEA		2/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0002171	PMID:26166480	PCS		1/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000708	PMID:32116545	PCS		15/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001419	PMID:32116545	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001518	PMID:32116545	PCS		10/34			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000407	PMID:32116545	PCS		3/32			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001317	PMID:32116545	PCS		6/32			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000505	PMID:32116545	PCS		2/10			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001956	PMID:32116545	PCS		10/38			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001257	PMID:32116545	PCS		5/38			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0001337	PMID:32116545	PCS		10/38			P	HPO:skoehler[2015-11-15];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0002500	PMID:32116545	PCS		15/32			P	HPO:probinson[2020-08-02];HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0002269	PMID:32116545	PCS		6/32			P	HPO:probinson[2020-08-02]
OMIM:300957	Intellectual developmental disorder, X-linked syndromic, Kumar type		HP:0000028	PMID:32116545	PCS		7/32			P	HPO:probinson[2020-08-02]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0002069	PMID:33999436	PCS		6/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0002521	PMID:33999436	PCS		2/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000486	PMID:33999436	PCS		1/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0010627	PMID:33999436	PCS		6/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0002384	PMID:33999436	PCS		4/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0001252	PMID:33999436	PCS		6/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0003593	PMID:33999436	PCS					C	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0032794	PMID:33999436	PCS		4/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0001270	PMID:33999436	PCS		7/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0012444	PMID:33999436	PCS		4/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0010845	PMID:33999436	PCS		6/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0033725	PMID:33999436	PCS		6/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000639	PMID:33999436	PCS		2/6			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000316	PMID:33999436	PCS		3/6			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000998	PMID:33999436	PCS		2/5			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000556	PMID:33999436	PCS		1/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0003623	PMID:33999436	PCS					C	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000054	PMID:33999436	PCS		2/3			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0001344	PMID:33999436	PCS		6/6			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0011195	PMID:33999436	PCS		6/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0032792	PMID:33999436	PCS		3/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000007	PMID:33999436	PCS					I	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0008245	PMID:33999436	PCS		7/7			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000527	PMID:33999436	PCS		5/6			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0000664	PMID:33999436	PCS		6/6			P	HPO:probinson[2022-08-31]
OMIM:619983	Developmental and epileptic encephalopathy 105 with hypopituitarism		HP:0001257	PMID:33999436	PCS		3/6			P	HPO:probinson[2022-08-31]
OMIM:610019	Cataract, autosomal recessive congenital 2		HP:0100018	PMID:21636066	PCS					P	HPO:probinson[2022-11-05]
OMIM:610019	Cataract, autosomal recessive congenital 2		HP:0003577	PMID:21636066	PCS					C	HPO:probinson[2022-11-05]
OMIM:610019	Cataract, autosomal recessive congenital 2		HP:0003593	PMID:21636066	PCS					C	HPO:probinson[2022-11-05]
OMIM:610019	Cataract, autosomal recessive congenital 2		HP:0000007	PMID:21636066	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-05]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0002166	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0000012	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0000496	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0001332	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0003487	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0001272	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0001260	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0000020	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0001251	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0002064	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0002061	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0011449	OMIM:607565	TAS					P	HPO:probinson[2012-04-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0011448	OMIM:607565	TAS					P	HPO:probinson[2012-04-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0007340	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0002839	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0001258	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0000006	OMIM:607565	IEA					I	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0001249	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:607565	Spastic paraplegia, ataxia, and impaired intellectual development		HP:0001347	OMIM:607565	IEA					P	HPO:iea[2009-02-17]
OMIM:615607	Immunodeficiency 17		HP:0005403	PMID:17277165	PCS		2/2			P	HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0002242	OMIM:615607	TAS		HP:0040283			P	HPO:skoehler[2014-02-25]
OMIM:615607	Immunodeficiency 17		HP:0001890	PMID:1635567	PCS		1/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0003593	PMID:1635567;PMID:17277165	PCS		3/3			C	HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0031123	OMIM:615607	TAS					P	HPO:probinson[2018-04-13]
OMIM:615607	Immunodeficiency 17		HP:0041063	PMID:1635567	PCS		2/2			P	HPO:probinson[2022-09-24];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0009098	PMID:17277165	PCS		2/2			P	HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0001508	PMID:1635567	PCS		1/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0003819	PMID:17277165	PCS		1/2			C	HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0000007	PMID:1635567	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0000964	OMIM:615607	TAS					P	HPO:skoehler[2014-02-25]
OMIM:615607	Immunodeficiency 17		HP:0000403	PMID:17277165	PCS		2/2			P	HPO:probinson[2017-05-29];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0002846	PMID:1635567	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0002205	PMID:17277165	PCS		2/2			P	HPO:skoehler[2014-02-25];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0001522	PMID:17277165	PCS		1/2			C	HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0005218	PMID:17277165	PCS		2/2			P	HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0005415	OMIM:615607	TAS					P	HPO:probinson[2017-05-29]
OMIM:615607	Immunodeficiency 17		HP:0002721	PMID:1635567	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2022-09-24]
OMIM:615607	Immunodeficiency 17		HP:0002028	PMID:17277165	PCS		2/2			P	HPO:probinson[2022-09-24]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001276	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002301	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003233	OMIM:267700	TAS					P	HPO:probinson[2013-01-07]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001250	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003573	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001252	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003075	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001251	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002240	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002383	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003073	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001290	OMIM:267700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0012229	OMIM:267700	TAS					P	HPO:probinson[2013-04-07]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0012156	OMIM:267700	TAS					P	HPO:probinson[2013-01-07]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0008151	OMIM:267700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001508	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0000737	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001903	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002716	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002516	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0000952	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001744	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003645	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001287	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002155	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001882	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001263	OMIM:267700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003141	OMIM:267700	TAS					P	HPO:probinson[2013-01-07]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003362	OMIM:267700	TAS					P	HPO:probinson[2013-01-07]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0011900	OMIM:267700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0003281	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0007430	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002902	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0000007	OMIM:267700	IEA					I	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002922	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001873	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0002445	OMIM:267700	IEA					P	HPO:iea[2009-02-17]
OMIM:267700	Hemophagocytic lymphohistiocytosis, familial, 1		HP:0001259	OMIM:267700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:190330	Trichomegaly		HP:0000518	OMIM:190330	IEA					P	HPO:iea[2009-02-17]
OMIM:190330	Trichomegaly		HP:0000007	OMIM:190330	TAS					I	HPO:skoehler[2015-12-30]
OMIM:190330	Trichomegaly		HP:0000527	OMIM:190330	IEA					P	HPO:iea[2009-02-17]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0002421	PMID:28168212	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0000486	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0001371	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0003198	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0006829	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0001252	PMID:28168212	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0003593	OMIM:618323	IEA					C	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0001270	PMID:28168212	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0025336	PMID:28168212	PCS		1/1			P	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0007941	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0003306	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0003700	PMID:28168212	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0003623	PMID:28168212	PCS		1/1			C	HPO:probinson[2023-02-18];HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0003403	PMID:28168212	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0002058	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0002015	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0002650	PMID:28168212	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0011968	PMID:28168212	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0001382	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0001260	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0001284	PMID:28168212	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0033383	PMID:28168212	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0002808	PMID:28168212	PCS		1/1			P	HPO:skoehler[2019-04-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0000007	PMID:28168212	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618323	Myasthenic syndrome, congenital, 25, presynaptic		HP:0001558	OMIM:618323	IEA					P	HPO:skoehler[2019-04-18]
OMIM:262650	Pituitary dwarfism IV		HP:0002750	OMIM:262650	IEA					P	HPO:iea[2009-02-17]
OMIM:262650	Pituitary dwarfism IV		HP:0000839	OMIM:262650	IEA					P	HPO:iea[2009-02-17]
OMIM:262650	Pituitary dwarfism IV		HP:0001939	OMIM:262650	IEA					P	HPO:iea[2009-02-17]
OMIM:262650	Pituitary dwarfism IV		HP:0000007	OMIM:262650	IEA					I	HPO:iea[2009-02-17]
OMIM:262650	Pituitary dwarfism IV		HP:0001510	OMIM:262650	IEA					P	HPO:iea[2009-02-17]
OMIM:608118	Zinc deficiency, transient neonatal		HP:0001596	PMID:17065149	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-07-15]
OMIM:608118	Zinc deficiency, transient neonatal		HP:0000964	OMIM:608118	TAS					P	HPO:skoehler[2013-01-21]
OMIM:608118	Zinc deficiency, transient neonatal		HP:0031831	PMID:17065149	PCS	HP:0003623	2/2			P	HPO:probinson[2020-07-15]
OMIM:608118	Zinc deficiency, transient neonatal		HP:0000006	PMID:17065149	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-07-15]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0003577	PMID:11791205	PCS		4/4			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0001252	OMIM:616326	TAS	HP:0003623				P	HPO:skoehler[2015-05-31]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0003391	PMID:11791205	PCS		2/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0001508	PMID:11791205	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0009046	PMID:11791205	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0000218	PMID:11791205	PCS		2/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0003403	PMID:11791205	PCS		3/3			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0003324	PMID:11791205	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0000276	OMIM:616326	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0003388	PMID:11791205	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0011968	OMIM:616326	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0011947	PMID:11791205	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0002033	PMID:11791205	PCS		3/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0033454	PMID:11791205	PCS		2/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0002093	OMIM:616326	TAS				HP:0025303	P	HPO:skoehler[2015-05-31]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0012378	PMID:11791205	PCS		2/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0030208	PMID:11791205	PCS		0/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0000508	PMID:11791205	PCS		4/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0001558	PMID:11791205	PCS		2/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0000007	PMID:11791205	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0002804	PMID:11791205	PCS		1/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0001319	OMIM:616326	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0002527	PMID:11791205	PCS		2/4			P	HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0001612	PMID:11791205	PCS		4/4			P	HPO:probinson[2022-09-06];HPO:probinson[2022-09-06]
OMIM:616326	Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency		HP:0002643	PMID:11791205	PCS		1/4			P	HPO:probinson[2022-09-06]
OMIM:619773	Immunodeficiency 95		HP:0002098	PMID:28606988	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0025179	PMID:28606988	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0032297	PMID:29018476	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0033166	PMID:28606988	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0003593	PMID:28606988	PCS		1/1			C	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0000007	PMID:28606988	PCS					I	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0001888	PMID:28606988	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0001954	PMID:29018476	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0002878	PMID:28606988	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0033214	PMID:28606988	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0032137	PMID:29018476	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619773	Immunodeficiency 95		HP:0002205	PMID:29018476	IEA		1/1			P	HPO:probinson[2022-05-29]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003676	PMID:11687801	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003236	PMID:11687801	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0002540	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0000365	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003355	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0001250	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0001252	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003593	PMID:11687801	PCS		3/4			C	HPO:probinson[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0001290	PMID:11687801	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003690	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003391	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0009141	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0000737	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0011463	PMID:11687801	PCS		1/4			C	HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0001349	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003128	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003700	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0002059	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003200	OMIM:609560	TAS					P	HPO:probinson[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0002134	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0011924	PMID:11687801	PCS					P	HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0011925	PMID:11687801	PCS					P	HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0002194	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0011923	PMID:11687801	PCS					P	HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003819	PMID:11687801	PCS		2/4			C	HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0000007	PMID:11687801	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0008347	PMID:11687801	PCS					P	HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0002747	PMID:11687801	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0008945	PMID:11687801	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:609560	Mitochondrial DNA depletion syndrome 2 (myopathic type)		HP:0003458	OMIM:609560	IEA					P	HPO:iea[2009-02-17]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0002365	PMID:19465910	PCS		5/5			P	HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001250	OMIM:610031	IEA					P	HPO:skoehler[2010-06-18]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0006927	OMIM:610031	IEA					P	HPO:iea[2009-02-17]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001491	OMIM:610031	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001274	PMID:19465910	PCS		2/5			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001270	PMID:19465910	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0012469	PMID:19465910	PCS		1/4			P	HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001328	OMIM:610031	IEA					P	HPO:iea[2009-02-17]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001302	OMIM:610031	TAS					P	HPO:skoehler[2012-11-16]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0007941	OMIM:610031	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001269	OMIM:610031	TAS					P	HPO:probinson[2009-02-17]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0006930	OMIM:610031	IEA					P	HPO:iea[2009-02-17]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001249	PMID:19465910	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0000478	OMIM:610031	IEA					P	HPO:iea[2009-02-17]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001320	PMID:19465910	PCS		2/5			P	HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0000252	PMID:19465910	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0002079	PMID:19465910	PCS		1/5			P	HPO:skoehler[2012-11-16]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001321	OMIM:610031	IEA					P	HPO:skoehler[2010-06-18]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0002197	PMID:19465910	PCS		2/4			P	HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001263	PMID:19465910	PCS		4/4			P	HPO:skoehler[2014-04-04];HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0002273	PMID:19465910	PCS		3/4			P	HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001339	OMIM:610031	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0001338	PMID:19465910	PCS		2/5			P	HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0002307	OMIM:610031	TAS					P	HPO:skoehler[2012-11-16]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0002126	PMID:19465910	PCS		5/5			P	HPO:probinson[2023-03-14]
OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7		HP:0000006	PMID:19465910	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-14]
OMIM:162830	Neutrophilia, hereditary		HP:0000006	PMID:19620628	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:162830	Neutrophilia, hereditary		HP:0002863	PMID:19620628	PCS		1/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-01-26]
OMIM:162830	Neutrophilia, hereditary		HP:0008318	OMIM:162830	IEA					P	HPO:iea[2009-02-17]
OMIM:162830	Neutrophilia, hereditary		HP:0001744	PMID:19620628	PCS		12/12			P	HPO:probinson[2023-01-26]
OMIM:162830	Neutrophilia, hereditary		HP:0012138	PMID:19620628	PCS					P	HPO:probinson[2023-01-26];HPO:probinson[2023-01-26]
OMIM:162830	Neutrophilia, hereditary		HP:0011897	PMID:19620628	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-26]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0000365	PMID:25572454	PCS		4/9			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0001156	PMID:25572454	PCS		3/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0000490	PMID:25572454	PCS		11/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0001252	PMID:25572454	PCS		5/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0001263	PMID:25572454	PCS		11/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0011800	PMID:25572454	PCS		8/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0001181	PMID:25572454	PCS		2/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0012385	PMID:25572454	PCS		4/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0000708	PMID:25572454	PCS		5/10			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0000316	PMID:25572454	PCS		4/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0000348	PMID:25572454	PCS		9/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0008872	PMID:25572454	PCS		10/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0002007	PMID:25572454	PCS		5/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0040019	PMID:25572454	PCS		6/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0001775	PMID:25572454	PCS		7/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0001511	PMID:25572454	PCS	HP:0011461	7/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0000322	PMID:25572454	PCS		5/11			P	HPO:probinson[2021-07-14]
OMIM:614257	Chromosome 20q11-q12 deletion syndrome		HP:0000006	PMID:21376300	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-09-20]
DECIPHER:35	WAGR 11p13 deletion syndrome		HP:0010461	DECIPHER:35	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:35	WAGR 11p13 deletion syndrome		HP:0000526	DECIPHER:35	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:35	WAGR 11p13 deletion syndrome		HP:0001249	DECIPHER:35	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:35	WAGR 11p13 deletion syndrome		HP:0009726	DECIPHER:35	IEA					P	HPO:skoehler[2013-05-29]
OMIM:266350	Red skin pigment anomaly of new guinea		HP:0001595	OMIM:266350	IEA					P	HPO:iea[2009-02-17]
OMIM:266350	Red skin pigment anomaly of new guinea		HP:0000639	OMIM:266350	IEA					P	HPO:iea[2009-02-17]
OMIM:266350	Red skin pigment anomaly of new guinea		HP:0000613	OMIM:266350	IEA					P	HPO:iea[2009-02-17]
OMIM:266350	Red skin pigment anomaly of new guinea		HP:0000007	OMIM:266350	IEA					I	HPO:iea[2009-02-17]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000054	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000252	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001671	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0003577	OMIM:612626	IEA					C	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000431	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000486	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001762	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0004322	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001156	OMIM:612626	TAS					P	HPO:skoehler[2014-11-26]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000581	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001263	OMIM:612626	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001508	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001518	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0005819	OMIM:612626	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0003745	OMIM:612626	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001511	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000047	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000028	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000325	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000347	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0000369	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612626	Chromosome 15q26-qter deletion syndrome		HP:0001249	OMIM:612626	IEA					P	HPO:skoehler[2010-06-19]
DECIPHER:21	Miller-Dieker syndrome (MDS)		HP:0000252	DECIPHER:21	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:21	Miller-Dieker syndrome (MDS)		HP:0001339	DECIPHER:21	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:21	Miller-Dieker syndrome (MDS)		HP:0011800	DECIPHER:21	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:21	Miller-Dieker syndrome (MDS)		HP:0001627	DECIPHER:21	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:21	Miller-Dieker syndrome (MDS)		HP:0002007	DECIPHER:21	IEA					P	HPO:skoehler[2013-05-29]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0002000	OMIM:155050	IEA					P	HPO:iea[2009-02-17]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0003196	OMIM:155050	IEA					P	HPO:iea[2009-02-17]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0004609	OMIM:155050	IEA					P	HPO:iea[2009-02-17]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0009882	OMIM:155050	TAS					P	HPO:probinson[2009-02-17]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0000689	OMIM:155050	IEA					P	HPO:iea[2009-02-17]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0005280	OMIM:155050	IEA					P	HPO:iea[2009-02-17]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0009748	OMIM:155050	IEA					P	HPO:iea[2009-02-17]
OMIM:155050	Maxillonasal dysplasia, Binder type		HP:0008428	OMIM:155050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0003577	PMID:34767620	PCS		1/4			C	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0003621	PMID:34767620	PCS		2/4			C	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0004313	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0003596	PMID:34767620	PCS		1/4			C	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0002091	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0031545	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0031413	PMID:34767620	PCS		4/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0001888	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0007588	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0008404	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0002216	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0005528	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0002745	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0002206	PMID:34767620	PCS		3/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0000006	PMID:34767620	PCS					I	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0001876	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:619767	Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6		HP:0002863	PMID:34767620	PCS		1/4			P	HPO:probinson[2022-05-18]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0003577	PMID:12022040	PCS		7/7			C	HPO:probinson[2021-03-07]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0001751	PMID:12022040	PCS		2/7			P	HPO:probinson[2021-03-07]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0001629	PMID:12022040	PCS	HP:0003577	2/7			P	HPO:probinson[2021-03-07]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0000407	PMID:12022040	PCS		6/7			P	HPO:probinson[2021-03-07]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0000627	PMID:12022040	PCS		7/7			P	HPO:probinson[2021-03-07]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0001636	PMID:12022040	PCS	HP:0003577	2/7			P	HPO:probinson[2021-03-07]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0004969	PMID:12022040	PCS	HP:0003577	5/7			P	HPO:probinson[2021-03-07]
OMIM:617992	Deafness, congenital heart defects, and posterior embryotoxon		HP:0000006	PMID:12022040	PCS					I	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0006801	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0003577	PMID:27103078	PCS		1/1			C	HPO:probinson[2023-02-25]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0008707	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000343	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000486	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000463	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-25]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0002066	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0001097	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0012110	OMIM:618479	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000639	PMID:27103078	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000319	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000718	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000557	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0001305	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000411	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0006610	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0001007	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000358	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000252	OMIM:618479	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0001344	PMID:27103078	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0001321	OMIM:618479	IEA				HP:0003680	P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0011825	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0001263	PMID:27103078	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000294	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0011230	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000007	PMID:27103078	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-25]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000546	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000527	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000505	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000664	PMID:27103078	PCS		1/1			P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000666	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome		HP:0000369	OMIM:618479	IEA					P	HPO:skoehler[2019-09-07]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0001397	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0002155	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0003233	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0004322	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0030685	PMID:24889630	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0003593	PMID:24889630	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0003074	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0041079	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0011462	PMID:24889630	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0000855	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0009125	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0000007	PMID:24889630	PCS					I	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0003635	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0005978	PMID:24889630	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0002910	PMID:24889630	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:620680	Lipodystrophy, congenital generalized, type 5		HP:0000842	PMID:24889630	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-21]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0003477	OMIM:610743	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0000486	OMIM:610743	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0002650	OMIM:610743	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0000365	PMID:17159980	PCS		0/53			P	HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0001761	OMIM:610743	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0001310	OMIM:610743	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0002395	PMID:17159980	PCS		14/53			P	HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0001272	PMID:17159980	PCS		34/34			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0002066	PMID:17159980	PCS		52/53			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0001260	PMID:17159980	PCS		53/53			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0003581	PMID:17159980	PCS		53/53			C	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0002070	PMID:17159980	PCS		52/53			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0002071	PMID:17159980	PCS		0/53			P	HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0012332	PMID:17159980	PCS		0/53			P	HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0000639	OMIM:610743	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0002808	OMIM:610743	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0000508	OMIM:610743	IEA					P	HPO:skoehler[2019-09-07]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0008003	PMID:17159980	PCS		23/51			P	HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0000007	PMID:17159980	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0000648	PMID:17159980	PCS		0/53			P	HPO:probinson[2023-04-14]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0001257	OMIM:610743	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:610743	Spinocerebellar ataxia, autosomal recessive 8		HP:0003677	OMIM:610743	TAS					C	HPO:skoehler[2015-12-30]
OMIM:126900	Dupuytren contracture 1		HP:0003676	OMIM:126900	TAS					C	HPO:skoehler[2009-02-17]
OMIM:126900	Dupuytren contracture 1		HP:0009473	OMIM:126900	IEA					P	HPO:iea[2009-02-17]
OMIM:126900	Dupuytren contracture 1		HP:0003581	OMIM:126900	TAS					C	HPO:probinson[2013-12-18]
OMIM:126900	Dupuytren contracture 1		HP:0003829	OMIM:126900	TAS					I	HPO:iea[2009-02-17]
OMIM:126900	Dupuytren contracture 1		HP:0000006	OMIM:126900	TAS					I	HPO:iea[2009-02-17]
OMIM:126900	Dupuytren contracture 1		HP:0005679	OMIM:126900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0002014	PMID:9419367	PCS		2/2			P	HPO:skoehler[2010-06-19]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0001541	PMID:9419367	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0002024	OMIM:602347	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0001394	PMID:9419367	PCS		2/2			P	HPO:skoehler[2010-06-19]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0002240	PMID:9419367	PCS		2/2			P	HPO:skoehler[2010-06-19]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0003593	PMID:9419367	PCS		2/2			C	HPO:skoehler[2010-06-19]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0030948	PMID:9419367	PCS		2/2			P	HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0012202	PMID:9419367	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0033196	PMID:9419367	PCS		1/2			P	HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0006580	PMID:9419367	PCS		2/2			P	HPO:skoehler[2013-06-11];HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0001408	PMID:9419367	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0000007	PMID:9419367	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0000989	PMID:9419367	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0001406	OMIM:602347	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0002910	PMID:9419367	PCS		2/2			P	HPO:skoehler[2010-06-19]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0000952	PMID:9419367	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-21]
OMIM:602347	Cholestasis, progressive familial intrahepatic, 3		HP:0001744	PMID:9419367	PCS		2/2			P	HPO:skoehler[2010-06-19]
OMIM:605428	Deafness, autosomal recessive 26		HP:0000407	PMID:29408807	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:605428	Deafness, autosomal recessive 26		HP:0000007	PMID:29408807	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-07]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001276	OMIM:608093	IEA					P	HPO:skoehler[2018-10-08]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0003577	OMIM:608093	TAS					C	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0002521	PMID:12872255	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001371	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001250	OMIM:608093	IEA					P	HPO:iea[2009-02-17]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0003075	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001252	PMID:12872255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0003593	PMID:12872255	PCS		1/1			C	HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001290	OMIM:608093	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0012469	PMID:12872255	PCS		1/1			P	HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000518	OMIM:608093	TAS					P	HPO:skoehler[2013-11-18]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000639	OMIM:608093	TAS					P	HPO:skoehler[2013-11-18]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000718	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000954	PMID:12872255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0002910	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001249	OMIM:608093	IEA					P	HPO:iea[2009-02-17]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000952	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000577	PMID:12872255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001347	OMIM:608093	TAS					P	HPO:skoehler[2013-11-18]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0003642	PMID:12872255	PCS		1/1			P	HPO:skoehler[2012-11-25];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000252	PMID:12872255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001263	PMID:12872255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0003186	OMIM:608093	TAS					P	HPO:skoehler[2013-11-18]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0002093	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0010781	OMIM:608093	IEA					P	HPO:skoehler[2010-06-20]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000007	PMID:12872255	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001976	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0004209	PMID:12872255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0002104	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000028	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0000347	OMIM:608093	IEA					P	HPO:iea[2009-02-17]
OMIM:608093	Congenital disorder of glycosylation, type Ij		HP:0001337	OMIM:608093	TAS		HP:0040283			P	HPO:skoehler[2012-11-25]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0030732	OMIM:618280	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0002089	PMID:29446546	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001651	OMIM:618280	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0002780	PMID:29446546	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000062	OMIM:618280	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0003010	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0011611	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0004383	OMIM:618280	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0011599	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001270	OMIM:618280	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0012741	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001629	PMID:29446546	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0002779	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001649	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001747	OMIM:618280	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001643	PMID:29446546	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001249	OMIM:618280	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000776	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000054	PMID:29446546	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000431	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0200128	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000151	OMIM:618280	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0031298	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0004691	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0031134	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0010773	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0011626	PMID:29446546	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0010479	PMID:29446546	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000808	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0034198	PMID:29446546	PCS		2/2			C	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001636	OMIM:618280	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001698	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000048	OMIM:618280	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0001631	OMIM:618280	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0002566	PMID:29446546	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0410259	PMID:29446546	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000105	PMID:29446546	PCS		1/2			P	HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000028	PMID:29446546	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-23]
OMIM:618280	Cardiac-Urogenital syndrome		HP:0000006	PMID:29446546	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-23]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0007913	OMIM:169150	IEA					P	HPO:iea[2009-02-17]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0000662	OMIM:169150	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0011506	OMIM:169150	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0025148	PMID:7710395	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-21]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0012508	OMIM:169150	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0000613	OMIM:169150	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0007663	PMID:7710395	PCS		3/6			P	HPO:probinson[2022-12-21]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0007963	PMID:7710395	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0007754	OMIM:169150	IEA					P	HPO:skoehler[2015-07-29]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0030506	PMID:7710395	PCS		5/6			P	HPO:probinson[2022-12-21]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0030825	PMID:7710395	PCS		1/6			P	HPO:probinson[2022-12-21]
OMIM:169150	Macular dystrophy, patterned, 1		HP:0000006	PMID:7710395	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-21]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001254	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001992	PMID:4073853	PCS		25/29			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001596	PMID:4073853	PCS		24/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001250	PMID:4073853	PCS		22/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001051	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001252	PMID:4073853	PCS		27/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0002240	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001251	PMID:4073853	PCS		18/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0003593	PMID:4073853	PCS					C	HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0100275	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0011463	PMID:4073853	PCS					C	HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001987	PMID:4073853	PCS		10/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0008872	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001744	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0000572	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0002014	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0410145	PMID:3930842	PCS					P	HPO:nvasilevsky[2018-03-12]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0002013	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001263	PMID:4073853;OMIM:253260	PCS		29/41			P	HPO:probinson[2022-04-30];HPO:probinson[2022-04-30];HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0001581	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0000407	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0000509	PMID:4073853	PCS		14/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0002506	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0000007	OMIM:253260	IEA					I	HPO:iea[2009-02-17]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0000648	PMID:4073853	PCS		17/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0000988	PMID:4073853	PCS		21/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0005979	PMID:4073853	PCS		25/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0002789	PMID:4073853	PCS		6/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253260	Biotinidase deficiencymultiple carboxylase deficiency, late-onset		HP:0002104	OMIM:253260	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0003577	PMID:12949970;PMID:7726174	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0001156	OMIM:148820	IEA					P	HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0100490	OMIM:148820	TAS					P	HPO:skoehler[2012-10-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0003691	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000581	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0001053	OMIM:148820	IEA					P	HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0012745	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0005274	PMID:12949970	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0010862	PMID:12949970	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0012785	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0012453	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000635	PMID:12949970	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0007443	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000537	PMID:12949970	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0030084	OMIM:148820	TAS					P	HPO:skoehler[2014-09-21]
OMIM:148820	Waardenburg syndrome, type 3		HP:0002216	PMID:7726174	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0009702	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0009129	PMID:12949970;PMID:7726174	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000358	PMID:12949970	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0001249	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0001100	OMIM:148820	IEA					P	HPO:skoehler[2010-06-20]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000252	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000431	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0002211	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0002251	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0010554	OMIM:148820	IEA					P	HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0001060	PMID:12949970;PMID:7726174	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000506	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:iea[2009-02-17];HPO:probinson[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000407	OMIM:148820	IEA					P	HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0009473	OMIM:148820	IEA					P	HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000426	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19];HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000007	OMIM:148820	IEA					I	HPO:skoehler[2010-06-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0002227	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000664	OMIM:148820	IEA					P	HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0001258	OMIM:148820	IEA					P	HPO:iea[2009-02-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0009933	PMID:12949970	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000303	OMIM:148820	IEA					P	HPO:skoehler[2010-06-18]
OMIM:148820	Waardenburg syndrome, type 3		HP:0000006	PMID:8447316	PCS					I	HPO:probinson[2020-07-17]
OMIM:148820	Waardenburg syndrome, type 3		HP:0002226	PMID:12949970;PMID:7726174	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-19]
OMIM:157900	Moebius syndrome		HP:0000044	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000286	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0009816	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000164	OMIM:157900	TAS		37%			P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0001491	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001171	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001608	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000316	OMIM:157900	TAS		25%			P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0009466	OMIM:157900	TAS					P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0003745	OMIM:157900	IEA					I	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0008734	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001763	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001188	OMIM:157900	TAS		20/20			P	HPO:probinson[2009-02-17];HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0002311	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0002312	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000054	OMIM:157900	TAS					P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0000298	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001260	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0002075	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0012385	OMIM:157900	TAS					P	HPO:skoehler[2013-10-22]
OMIM:157900	Moebius syndrome		HP:0001739	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000568	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000565	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000006	OMIM:157900	IEA					I	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0008947	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001597	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0002365	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001156	OMIM:157900	TAS					P	HPO:skoehler[2014-11-26]
OMIM:157900	Moebius syndrome		HP:0001270	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000932	OMIM:157900	TAS					P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0008872	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001349	OMIM:157900	TAS					P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0000218	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0030084	OMIM:157900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:157900	Moebius syndrome		HP:0000377	OMIM:157900	TAS					P	HPO:probinson[2015-03-29]
OMIM:157900	Moebius syndrome		HP:0006897	OMIM:157900	IEA					P	HPO:skoehler[2019-02-22]
OMIM:157900	Moebius syndrome		HP:0009803	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000577	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0002015	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001762	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000750	OMIM:157900	TAS		55%			P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0001288	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0002098	OMIM:157900	TAS					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000193	OMIM:157900	TAS		11%			P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0000470	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0005280	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0009830	OMIM:157900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:157900	Moebius syndrome		HP:0002804	OMIM:157900	TAS		6%			P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0005914	OMIM:157900	TAS					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0001159	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:157900	Moebius syndrome		HP:0000347	OMIM:157900	TAS		64%			P	HPO:probinson[2012-03-26]
OMIM:157900	Moebius syndrome		HP:0002644	OMIM:157900	IEA					P	HPO:probinson[2009-02-17]
OMIM:612961	Multiple synostoses syndrome 3		HP:0001440	PMID:19589401	PCS					P	HPO:probinson[2013-02-17]
OMIM:612961	Multiple synostoses syndrome 3		HP:0000175	OMIM:612961	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612961	Multiple synostoses syndrome 3		HP:0010621	OMIM:612961	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:612961	Multiple synostoses syndrome 3		HP:0003041	PMID:19589401	PCS					P	HPO:probinson[2013-02-17]
OMIM:612961	Multiple synostoses syndrome 3		HP:0008080	OMIM:612961	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:612961	Multiple synostoses syndrome 3		HP:0011304	OMIM:612961	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:612961	Multiple synostoses syndrome 3		HP:0006064	PMID:19589401	PCS					P	HPO:probinson[2016-02-01]
OMIM:612961	Multiple synostoses syndrome 3		HP:0010055	OMIM:612961	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:612961	Multiple synostoses syndrome 3		HP:0002967	PMID:19589401	PCS					P	HPO:probinson[2013-02-17]
OMIM:612961	Multiple synostoses syndrome 3		HP:0000268	OMIM:612961	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:612961	Multiple synostoses syndrome 3		HP:0009701	PMID:19589401	PCS					P	HPO:probinson[2013-02-17]
OMIM:612961	Multiple synostoses syndrome 3		HP:0000520	OMIM:612961	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:612961	Multiple synostoses syndrome 3		HP:0000006	PMID:19589401	PCS					I	HPO:probinson[2013-02-17]
OMIM:619834	Ovarian dysgenesis 10		HP:0008209	PMID:34402903	PCS		2/2			P	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0003621	PMID:34402903	PCS		2/2			C	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0011969	PMID:34402903	PCS		2/2			P	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0008232	PMID:34402903	PCS		2/2			P	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0000007	PMID:34402903	PCS					I	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0000823	PMID:34402903	PCS		2/2			P	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0008214	PMID:34402903	PCS		2/2			P	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0010464	PMID:34402903	PCS		1/2			P	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0000786	PMID:34402903	PCS		2/2			P	HPO:probinson[2022-06-13]
OMIM:619834	Ovarian dysgenesis 10		HP:0008724	PMID:34402903	PCS		1/2			P	HPO:probinson[2022-06-13]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0002345	OMIM:616291	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0003676	PMID:25205112	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0004322	OMIM:616291	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0001310	PMID:25205112	PCS		3/3			P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0031936	PMID:25205112	PCS		3/3			P	HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0001272	OMIM:616291	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0001260	OMIM:616291	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0002066	PMID:25205112	PCS		3/3			P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0001251	PMID:25205112	PCS		3/3			P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0002075	PMID:25205112	PCS		3/3			P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0001270	PMID:25205112	PCS		3/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0002070	PMID:25205112	PCS		3/3			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0012046	PMID:25205112	PCS		3/3			P	HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0000639	OMIM:616291	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0011463	PMID:25205112	PCS		3/3			C	HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0000407	PMID:25205112	PCS		3/3			P	HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0000957	PMID:25205112	PCS		2/3			P	HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0000007	PMID:25205112	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0001756	PMID:25205112	PCS		1/1			P	HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0002522	PMID:25205112	PCS		3/3			P	HPO:probinson[2023-06-10]
OMIM:616291	Lichtenstein-Knorr syndrome		HP:0006855	PMID:25205112	PCS		1/3			P	HPO:probinson[2023-06-10]
OMIM:212200	CARNOSINEMIA		HP:0003167	OMIM:212200	IEA					P	HPO:iea[2009-02-17]
OMIM:212200	CARNOSINEMIA		HP:0002123	OMIM:212200	IEA					P	HPO:iea[2009-02-17]
OMIM:212200	CARNOSINEMIA		HP:0000007	OMIM:212200	IEA					I	HPO:iea[2009-02-17]
OMIM:212200	CARNOSINEMIA		HP:0001249	OMIM:212200	IEA					P	HPO:iea[2009-02-17]
OMIM:161530	Nasal hyperpigmentation, familial transverse		HP:0000953	OMIM:161530	TAS					P	HPO:probinson[2009-02-17]
OMIM:161530	Nasal hyperpigmentation, familial transverse		HP:0000006	OMIM:161530	IEA					I	HPO:iea[2009-02-17]
OMIM:614486	Thrombophilia due to thrombomodulin defect		HP:0003581	PMID:7811989	PCS		2/2			C	HPO:probinson[2022-10-02]
OMIM:614486	Thrombophilia due to thrombomodulin defect		HP:0100724	PMID:7811989	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-02]
OMIM:614486	Thrombophilia due to thrombomodulin defect		HP:0002625	PMID:7811989	PCS		1/2			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-02]
OMIM:614486	Thrombophilia due to thrombomodulin defect		HP:0000006	PMID:7811989	PCS					I	HPO:probinson[2022-10-02]
OMIM:614486	Thrombophilia due to thrombomodulin defect		HP:0002204	PMID:7811989	PCS		1/2			P	HPO:probinson[2022-10-02]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002421	PMID:24515575;PMID:19641205	PCS		2/3			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0003577	PMID:24515575	PCS		1/2			C	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0000189	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0005235	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001250	PMID:24515575	PCS		2/2			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001252	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0006829	PMID:19641205	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0006808	PMID:19641205	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0003593	PMID:24515575;PMID:19641205	PCS		2/3			C	HPO:probinson[2022-07-19];HPO:skoehler[2010-06-19];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0012708	PMID:19641205	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0011335	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0032656	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0011261	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0000817	PMID:19641205	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0000316	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0000954	PMID:24515575	PCS		2/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0003803	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001667	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0008936	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0032989	PMID:19641205	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0005469	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001561	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001344	PMID:24515575;PMID:19641205	PCS		3/3			P	HPO:probinson[2022-07-19];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002133	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0031936	PMID:24515575	PCS		2/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002373	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002230	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002197	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001263	PMID:24515575;PMID:19641205	PCS		3/3			P	HPO:probinson[2022-07-19];HPO:skoehler[2010-06-19];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002151	PMID:19641205	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0005484	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001182	PMID:24515575	PCS		2/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0032988	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0011451	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0032792	PMID:19641205	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0007034	PMID:19641205	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0000007	PMID:19641205	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002705	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0200134	PMID:24515575;PMID:19641205	PCS		2/3			P	HPO:probinson[2022-07-19];HPO:skoehler[2017-07-13];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002307	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0000389	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0000300	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001257	PMID:19641205	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0002104	PMID:19641205	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0003557	PMID:24515575	PCS		1/2			P	HPO:probinson[2022-07-19]
OMIM:612949	Epileptic encephalopathy, early infantile, 39		HP:0001336	PMID:19641205	PCS		1/1			P	HPO:probinson[2022-07-19]
OMIM:216700	Collagenosis, familial reactive perforating		HP:0001939	OMIM:216700	IEA					P	HPO:iea[2009-02-17]
OMIM:216700	Collagenosis, familial reactive perforating		HP:0000007	OMIM:216700	IEA					I	HPO:iea[2009-02-17]
OMIM:216700	Collagenosis, familial reactive perforating		HP:0000951	OMIM:216700	IEA					P	HPO:iea[2009-02-17]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0002069	PMID:33731878	PCS		2/3			P	HPO:probinson[2021-09-18]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0000750	PMID:29100083;PMID:33731878	PCS		4/6			P	HPO:probinson[2021-09-18];HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0002353	PMID:29100083	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0002123	PMID:29100083	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0001250	PMID:29100083	PCS	HP:0003593	3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0002384	PMID:33731878	PCS		1/3			P	HPO:probinson[2021-09-18]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0001260	PMID:29100083	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0002066	PMID:29100083	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0002121	PMID:33731878	PCS		2/3			P	HPO:probinson[2021-09-18]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0001263	PMID:29100083	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0001251	PMID:33731878	PCS		2/2		HP:0012825	P	HPO:probinson[2021-09-18]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0032794	PMID:33731878	PCS		1/3			P	HPO:probinson[2021-09-18]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0001270	PMID:29100083;PMID:33731878	PCS		2/6			P	HPO:probinson[2021-09-18];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0011463	PMID:33731878	PCS		3/3			C	HPO:probinson[2021-09-18]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0000729	PMID:29100083	PCS		1/3			P	HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0200134	PMID:29100083	PCS		3/3			P	HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0000006	PMID:29100083	PCS		20/20			I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2021-09-18];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0001249	PMID:29100083;PMID:33731878	PCS		5/5			P	HPO:probinson[2021-09-18];HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:617831	Intellectual developmental disorder, autosomal dominant 55, with seizures		HP:0001337	PMID:29100083;PMID:33731878	PCS		5/6			P	HPO:probinson[2021-09-18];HPO:skoehler[2018-10-08];HPO:probinson[2019-02-14]
OMIM:620045	Intestinal dysmotility syndrome		HP:0002014	PMID:32487539	PCS		2/2			P	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0030897	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0001561	PMID:32487539	PCS		2/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0002587	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0003577	PMID:32487539	PCS		1/2			C	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0011968	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0001252	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0003270	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0008081	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0000518	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0001508	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0000007	PMID:32487539	PCS					I	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0000218	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0001824	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0000289	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0000369	PMID:32487539	PCS		1/2			P	HPO:probinson[2022-10-03]
OMIM:620045	Intestinal dysmotility syndrome		HP:0003623	PMID:32487539	PCS		1/2			C	HPO:probinson[2022-10-03]
OMIM:617825	Glucocorticoid deficiency 5		HP:0008163	PMID:24601690	PCS		7/7			P	HPO:probinson[2019-06-13];HPO:probinson[2019-06-13]
OMIM:617825	Glucocorticoid deficiency 5		HP:0031074	PMID:24601690	IEA					P	HPO:probinson[2019-06-13]
OMIM:617825	Glucocorticoid deficiency 5		HP:0000007	PMID:24601690	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:617825	Glucocorticoid deficiency 5		HP:0000953	PMID:24601690	PCS		5/7			P	HPO:probinson[2019-06-13]
OMIM:300604	Premature ovarian failure 2B		HP:0008209	PMID:16773570	PCS		5/5			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0000939	PMID:16773570	PCS		2/5			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0000164	PMID:16773570	PCS		2/5			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0001419	PMID:16773570	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0034344	PMID:16773570	PCS					I	HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0008222	PMID:16773570	PCS		5/5			P	HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0011462	PMID:16773570	PCS		5/5			C	HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0000823	PMID:16773570	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:300604	Premature ovarian failure 2B		HP:0000786	PMID:16773570	PCS		5/5			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-10-30]
OMIM:168500	Parietal foramina		HP:0000175	OMIM:168500	IEA					P	HPO:iea[2009-02-17]
OMIM:168500	Parietal foramina		HP:0002697	OMIM:168500;PMID:10742103	PCS		19/20			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-03]
OMIM:168500	Parietal foramina		HP:0001250	OMIM:168500	IEA					P	HPO:iea[2009-02-17]
OMIM:168500	Parietal foramina		HP:0007385	OMIM:168500	IEA					P	HPO:iea[2009-02-17]
OMIM:168500	Parietal foramina		HP:0000592	PMID:10742103	PCS		1/10			P	HPO:probinson[2022-09-03]
OMIM:168500	Parietal foramina		HP:0002084	OMIM:168500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:168500	Parietal foramina		HP:0002315	OMIM:168500	IEA					P	HPO:iea[2009-02-17]
OMIM:168500	Parietal foramina		HP:0002645	PMID:10742103	PCS		1/10			P	HPO:probinson[2022-09-03]
OMIM:168500	Parietal foramina		HP:0000256	PMID:10742103	PCS		1/10			P	HPO:probinson[2022-09-03]
OMIM:168500	Parietal foramina		HP:0000006	PMID:10742103	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:168500	Parietal foramina		HP:0000204	OMIM:168500	IEA					P	HPO:iea[2009-02-17]
OMIM:619808	Deafness, autosomal dominant 83		HP:0003621	PMID:33268592	PCS		2/7			C	HPO:probinson[2022-06-17]
OMIM:619808	Deafness, autosomal dominant 83		HP:0008619	PMID:33268592	PCS		7/7			P	HPO:probinson[2022-06-17]
OMIM:619808	Deafness, autosomal dominant 83		HP:0003596	PMID:33268592	PCS		1/7			C	HPO:probinson[2022-06-17]
OMIM:619808	Deafness, autosomal dominant 83		HP:0011462	PMID:33268592	PCS		5/7			C	HPO:probinson[2022-06-17];HPO:probinson[2022-06-17]
OMIM:619808	Deafness, autosomal dominant 83		HP:0000006	PMID:33268592	PCS					I	HPO:probinson[2022-06-17]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0006350	OMIM:125400	IEA					P	HPO:iea[2009-02-17]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0000691	PMID:22152679	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-06]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0006297	PMID:22152679	PCS		2/2			P	HPO:probinson[2022-10-06]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0000679	PMID:22152679	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-06]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0000007	PMID:22152679	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-06]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0000700	OMIM:125400	IEA					P	HPO:iea[2009-02-17]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0006336	PMID:22152679	PCS		2/2			P	HPO:probinson[2022-10-06]
OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth		HP:0000677	PMID:22152679	PCS		2/2			P	HPO:probinson[2022-10-06]
OMIM:249210	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1		HP:0001562	PMID:28602422	PCS					P	HPO:probinson[2020-06-27]
OMIM:249210	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1		HP:0010956	PMID:28602422	PCS	HP:0030674				P	HPO:probinson[2020-06-27]
OMIM:249210	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1		HP:0000072	PMID:28602422	PCS					P	HPO:probinson[2020-06-27]
OMIM:249210	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1		HP:0007430	PMID:28602422	PCS	HP:0030674				P	HPO:probinson[2020-06-27]
OMIM:249210	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1		HP:0000007	PMID:28602422	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:249210	Megacystis-microcolon-intestinal hypoperistalsis syndrome 1		HP:0002566	PMID:28602422	PCS	HP:0030674				P	HPO:probinson[2020-06-27]
OMIM:603688	Prostate cancer/brain cancer susceptibility		HP:0100006	OMIM:603688	IEA					P	HPO:skoehler[2013-01-14]
OMIM:603688	Prostate cancer/brain cancer susceptibility		HP:0012125	OMIM:603688	IEA					P	HPO:skoehler[2013-01-09]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0002153	PMID:11498583	PCS		10/10			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-03-25]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0008242	PMID:11498583	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-03-25]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0004918	OMIM:614492	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0032066	PMID:11498583	PCS		10/10			P	HPO:probinson[2023-03-25]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0003351	PMID:11498583	PCS		10/10			P	HPO:probinson[2023-03-25]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0000822	PMID:11498583	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-25]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0011423	PMID:11498583	PCS		10/10			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-03-25]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0000006	PMID:11498583	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-25]
OMIM:614492	Pseudohypoaldosteronism, type IIC		HP:0001942	OMIM:614492	TAS					P	HPO:skoehler[2013-01-22]
OMIM:200610	Achondrogenesis, type II		HP:0000343	PMID:34573377	PCS		1/1			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0001552	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:6000653	PMID:28744080	PCS					P	HPO:probinson[2024-05-09]
OMIM:200610	Achondrogenesis, type II		HP:0001090	PMID:34573377	PCS		1/1			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0003826	OMIM:200610	IEA					C	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0008873	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0001789	OMIM:200610	TAS					P	HPO:probinson[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0000773	OMIM:200610	TAS					P	HPO:probinson[2013-04-12]
OMIM:200610	Achondrogenesis, type II		HP:0000476	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0001248	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0003026	PMID:34573377	PCS		1/1		HP:0012828	P	HPO:probinson[2012-05-08];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0003521	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0001760	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0001561	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0000175	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0005622	OMIM:200610	TAS					P	HPO:probinson[2012-05-08]
OMIM:200610	Achondrogenesis, type II		HP:6000866	PMID:24144387	PCS					P	HPO:probinson[2024-08-04]
OMIM:200610	Achondrogenesis, type II		HP:6000867	PMID:24144387	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:200610	Achondrogenesis, type II		HP:0000969	OMIM:200610	IEA					P	HPO:skoehler[2010-06-20]
OMIM:200610	Achondrogenesis, type II		HP:0034198	PMID:34573377	PCS		1/1			C	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0000308	PMID:34573377	PCS		1/1			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0000888	OMIM:200610	TAS					P	HPO:probinson[2013-04-12]
OMIM:200610	Achondrogenesis, type II		HP:0001538	PMID:34573377	PCS		1/1			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0004605	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0002007	PMID:34573377	PCS		1/1			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0002866	OMIM:200610	IEA					P	HPO:iea[2009-02-17]
OMIM:200610	Achondrogenesis, type II		HP:0000248	PMID:34573377	PCS		1/1			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:200610	Achondrogenesis, type II		HP:0000006	PMID:2572591	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-11]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0004324	OMIM:615954	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0001442	OMIM:615954	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0003581	PMID:24708098	PCS					C	HPO:probinson[2020-09-05]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0003074	OMIM:615954	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0012378	OMIM:615954	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0012743	OMIM:615954	TAS		HP:0040283			P	HPO:skoehler[2015-01-20]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0000939	OMIM:615954	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0008231	PMID:24708098	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2020-09-05]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0000716	OMIM:615954	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0012030	PMID:24283224	PCS		15/15			P	HPO:probinson[2020-09-05]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0000822	OMIM:615954	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0002920	PMID:24283224	PCS		18/18			P	HPO:probinson[2020-09-05]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0003118	PMID:24283224	PCS		15/18			P	HPO:probinson[2020-09-05]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0000311	OMIM:615954	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615954	ACTH-independent macronodular adrenal hyperplasia 2		HP:0000006	PMID:24708098	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-09-05]
OMIM:309620	Christianson syndrome		HP:0002652	OMIM:309620	IEA					P	HPO:skoehler[2015-12-30]
OMIM:309620	Christianson syndrome		HP:0000431	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0002023	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0002650	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0004322	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0005487	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0002949	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0005819	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0001417	OMIM:309620	IEA					I	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0008467	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0006897	OMIM:309620	TAS		20/20			P	HPO:iea[2009-02-17];HPO:skoehler[2012-10-17]
OMIM:309620	Christianson syndrome		HP:0001249	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:309620	Christianson syndrome		HP:0001952	OMIM:309620	IEA					P	HPO:iea[2009-02-17]
OMIM:159050	Muscular dystrophy, pseudohypertrophic, with internalized capillaries		HP:0003560	OMIM:159050	TAS					P	HPO:skoehler[2009-02-17]
OMIM:159050	Muscular dystrophy, pseudohypertrophic, with internalized capillaries		HP:0030230	OMIM:159050	TAS					P	HPO:probinson[2015-06-02]
OMIM:159050	Muscular dystrophy, pseudohypertrophic, with internalized capillaries		HP:0001324	OMIM:159050	IEA					P	HPO:iea[2009-02-17]
OMIM:159050	Muscular dystrophy, pseudohypertrophic, with internalized capillaries		HP:0000006	OMIM:159050	IEA					I	HPO:iea[2009-02-17]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0002421	PMID:21150889	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0001263	PMID:21150889	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0001252	PMID:21150889	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0003593	OMIM:618243	IEA					C	HPO:skoehler[2019-02-15]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0002490	PMID:21150889	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0032653	PMID:21150889	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0002093	PMID:21150889	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0011923	PMID:21150889	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0001639	PMID:21150889	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0000007	PMID:21150889	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0025116	PMID:21150889	PCS		1/1			P	HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0001511	OMIM:618243	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0003128	PMID:21150889	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-05]
OMIM:618243	Mitochondrial complex I deficiency, nuclear type 22		HP:0003623	PMID:21150889	PCS		1/1			C	HPO:probinson[2023-03-05]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0002037	PMID:24746753	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0003212	PMID:24746753	PCS	HP:0011463	1/1			P	HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0100280	PMID:24746753	PCS	HP:0011463	1/1			P	HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0030388	PMID:24746753	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0011839	PMID:24746753	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0003593	PMID:24746753	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0012378	PMID:24746753	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0001508	PMID:24746753	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0100759	PMID:24746753	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0033343	PMID:24746753	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0032154	PMID:24746753	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0000007	PMID:24746753	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0002205	PMID:24746753	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0001510	PMID:24746753	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-09]
OMIM:615767	Immunodeficiency, common variable, 11		HP:0004315	PMID:24746753	PCS	HP:0011463	1/1			P	HPO:probinson[2021-05-09]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0001156	OMIM:114150	TAS					P	HPO:probinson[2012-06-09]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0001161	OMIM:114150	IEA					P	HPO:iea[2009-02-17]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0000020	OMIM:114150	IEA					P	HPO:iea[2009-02-17]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0001153	OMIM:114150	IEA					P	HPO:iea[2009-02-17]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0001159	OMIM:114150	IEA					P	HPO:iea[2009-02-17]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0005879	OMIM:114150	IEA					P	HPO:iea[2009-02-17]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0000006	OMIM:114150	IEA					I	HPO:iea[2009-02-17]
OMIM:114150	CAMPTOBRACHYDACTYLY		HP:0001831	OMIM:114150	TAS					P	HPO:probinson[2012-06-09]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0002861	OMIM:278740	TAS					P	HPO:probinson[2013-03-11]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0000992	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0003079	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0004334	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0000491	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0006739	OMIM:278740	TAS					P	HPO:probinson[2013-03-11]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0002671	OMIM:278740	TAS					P	HPO:probinson[2013-03-11]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0000509	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0000613	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0001009	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0000007	OMIM:278740	IEA					I	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0000656	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0001029	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:278740	Xeroderma pigmentosum, complementation group E		HP:0000621	OMIM:278740	IEA					P	HPO:probinson[2009-02-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0001251	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0001081	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0010871	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0001082	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0011993	PMID:4076245	PCS					P	HPO:probinson[2012-07-19]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0011981	OMIM:613470	TAS					P	HPO:probinson[2012-07-18]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0000007	OMIM:613470	TAS					I	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0001324	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0000952	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0001744	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0001249	OMIM:613470	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0003568	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0001930	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:613470	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerasedeficiency		HP:0005525	OMIM:613470	TAS					P	HPO:probinson[2012-07-17]
OMIM:617616	Skraban-Deardorff syndrome		HP:0025186	PMID:28686853	PCS		1/15			P	HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001773	PMID:28686853	PCS		2/8			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000486	PMID:28686853	PCS		8/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001250	OMIM:617616	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001252	PMID:28686853	PCS		9/12			P	HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002020	PMID:28686853	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0003593	PMID:28686853	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002064	OMIM:617616	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0003194	PMID:28686853	PCS		5/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000280	PMID:28686853	PCS		12/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0010800	PMID:28686853	PCS		11/15			P	HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001090	PMID:28686853	PCS		11/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0033725	PMID:28686853	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0012471	PMID:28686853	PCS		9/14			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000316	PMID:28686853	PCS		5/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0009623	PMID:28686853	PCS		1/10			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002019	OMIM:617616;PMID:28686853	PCS		14/22			P	ORCID:0000-0002-0736-9199[2024-06-28];HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001007	PMID:28686853	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001249	PMID:28686853	PCS		15/15			P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000175	PMID:28686853	PCS		1/15			P	HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001344	OMIM:617616	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002079	OMIM:617616	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0011968	PMID:28686853	PCS		6/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000293	PMID:28686853	PCS		11/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000490	PMID:28686853	PCS		0/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001263	PMID:28686853	PCS		15/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0011800	PMID:28686853	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0012020	PMID:28686853	PCS		1/15			P	HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000646	PMID:28686853	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000403	PMID:28686853	PCS		4/10			P	HPO:skoehler[2019-04-18]
OMIM:617616	Skraban-Deardorff syndrome		HP:0004209	PMID:28686853	PCS		4/12			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0009933	PMID:28686853	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000520	PMID:28686853	PCS		3/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000322	PMID:28686853	PCS		7/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000006	PMID:28686853	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000248	PMID:28686853	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0005338	PMID:28686853	PCS		6/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000687	PMID:28686853	PCS		13/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000341	PMID:28686853	PCS		6/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000582	PMID:28686853	PCS		4/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000463	PMID:28686853	PCS		8/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000540	PMID:28686853	PCS		5/13			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0040082	PMID:28686853	PCS		10/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001508	PMID:28686853	PCS		5/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001629	PMID:28686853	PCS		1/15			P	HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000219	PMID:28686853	PCS		3/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002119	OMIM:617616	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000455	PMID:28686853	PCS		11/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0006335	PMID:28686853	PCS		4/9			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000212	PMID:28686853	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000179	PMID:28686853	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000336	PMID:28686853	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000215	PMID:28686853	PCS		13/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000154	PMID:28686853	PCS		10/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002136	OMIM:617616	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0031936	OMIM:617616	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617616	Skraban-Deardorff syndrome		HP:0001761	PMID:28686853	PCS		2/15			P	HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002373	PMID:28686853	PCS		9/13			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0005280	PMID:28686853	PCS		5/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0012683	PMID:28686853	PCS		3/15			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0430028	PMID:28686853	PCS		13/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0002007	PMID:28686853	PCS		0/14			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0200055	PMID:28686853	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000347	PMID:28686853	PCS		5/15			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617616	Skraban-Deardorff syndrome		HP:0000545	PMID:28686853	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-06-28]
OMIM:609428	Tukel syndrome		HP:0007936	OMIM:609428	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0001491	OMIM:609428	IEA					P	HPO:iea[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0004231	OMIM:609428	IEA					P	HPO:iea[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0000508	OMIM:609428	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0006210	OMIM:609428	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0000007	OMIM:609428	IEA					I	HPO:iea[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0001159	OMIM:609428	IEA					P	HPO:skoehler[2010-06-20]
OMIM:609428	Tukel syndrome		HP:0007831	OMIM:609428	IEA					P	HPO:iea[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0009702	OMIM:609428	IEA					P	HPO:iea[2009-02-17]
OMIM:609428	Tukel syndrome		HP:0001477	OMIM:609428	IEA					P	HPO:iea[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0000819	OMIM:167800	IEA					P	HPO:iea[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0002202	OMIM:167800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:167800	Pancreatitis, hereditary		HP:0005213	OMIM:167800	IEA					P	HPO:iea[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0001738	OMIM:167800	IEA					P	HPO:iea[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0002570	OMIM:167800	IEA					P	HPO:iea[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0001977	OMIM:167800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:167800	Pancreatitis, hereditary		HP:0001945	OMIM:167800	TAS					P	HPO:probinson[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0000006	OMIM:167800	IEA					I	HPO:iea[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0001733	OMIM:167800	IEA					P	HPO:iea[2009-02-17]
OMIM:167800	Pancreatitis, hereditary		HP:0002027	OMIM:167800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:167800	Pancreatitis, hereditary		HP:0005206	OMIM:167800	IEA					P	HPO:iea[2009-02-17]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0025474	PMID:30528822	PCS	HP:0003593	18/18			P	HPO:probinson[2020-07-23];HPO:probinson[2024-03-15]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0001595	PMID:30528822	PCS		0/18			P	HPO:probinson[2024-03-15]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0001036	PMID:30528822	PCS					P	HPO:probinson[2020-07-23]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0006482	PMID:30528822	PCS		0/18			P	HPO:probinson[2024-03-15]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0003593	PMID:30528822	PCS		18/18			C	HPO:probinson[2024-03-15]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0011675	PMID:30528822	PCS		0/18			P	HPO:probinson[2020-07-23];HPO:probinson[2024-03-15]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0000989	PMID:30528822	PCS					P	HPO:probinson[2020-07-23]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0000006	PMID:30528822	PCS					I	HPO:probinson[2020-07-23];HPO:probinson[2020-07-23]
OMIM:618531	Erythrokeratodermia veriabilis et progressiva 6		HP:0031190	PMID:30528822	PCS					P	HPO:probinson[2020-07-23]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000341	PMID:28288113	PCS		1/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000582	PMID:28288113	PCS		1/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0003577	PMID:28288113	PCS		6/6			C	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002023	PMID:28288113	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0004322	PMID:28288113	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0010747	PMID:28288113	PCS		1/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000460	OMIM:617602	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0003196	OMIM:617602	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001508	PMID:28288113	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001629	PMID:28288113	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000319	PMID:28288113	PCS		1/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0012450	PMID:28288113	PCS		3/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002616	PMID:28288113	PCS		2/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000337	OMIM:617602	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000678	PMID:28288113	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000218	PMID:28288113	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000977	PMID:28288113	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002714	PMID:28288113	PCS		1/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001763	PMID:28288113	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000776	PMID:28288113	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001166	PMID:28288113	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000670	PMID:28288113	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0003189	OMIM:617602	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002650	PMID:28288113	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000233	PMID:28288113	PCS		3/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000331	PMID:28288113	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002010	OMIM:617602	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001382	PMID:28288113	PCS		3/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000490	PMID:28288113	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001263	PMID:28288113	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001680	PMID:28288113	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0012385	OMIM:617602	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002808	PMID:28288113	PCS		1/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000965	PMID:28288113	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000767	PMID:28288113	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000307	OMIM:617602	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0004209	PMID:28288113	PCS		2/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001511	PMID:28288113	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002007	PMID:28288113	PCS		2/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001852	PMID:28288113	PCS		1/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0006522	PMID:28288113	PCS		2/6			P	HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0001631	PMID:28288113	PCS		3/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000047	PMID:28288113	PCS		2/4	MALE		P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000006	PMID:28288113	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000028	PMID:28288113	PCS		1/4	MALE		P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0002566	PMID:28288113	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617602	Congenital heart defects and skeletal malformations syndrome		HP:0000963	PMID:28288113	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:607411	Patent ductus arteriosus 1		HP:0000007	OMIM:607411	TAS					I	HPO:skoehler[2017-07-13]
OMIM:607411	Patent ductus arteriosus 1		HP:0001643	OMIM:607411	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613464	Retinitis pigmentosa 51		HP:0000077	PMID:20451172	PCS		0/4			P	HPO:probinson[2013-06-02];HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0007737	PMID:20451172	PCS		4/4			P	HPO:probinson[2013-06-02]
OMIM:613464	Retinitis pigmentosa 51		HP:0000662	OMIM:613464	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613464	Retinitis pigmentosa 51		HP:0000980	OMIM:613464	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613464	Retinitis pigmentosa 51		HP:0001263	PMID:20451172	PCS		0/4			P	HPO:probinson[2013-06-02];HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0010442	PMID:20451172	PCS		0/4			P	HPO:probinson[2013-06-02];HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0011003	OMIM:613464	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613464	Retinitis pigmentosa 51		HP:0011463	PMID:20451172	PCS		4/4			C	HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0000608	OMIM:613464	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613464	Retinitis pigmentosa 51		HP:0008323	OMIM:613464	TAS					P	HPO:probinson[2013-06-02]
OMIM:613464	Retinitis pigmentosa 51		HP:0000613	OMIM:613464	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613464	Retinitis pigmentosa 51		HP:0000007	PMID:20451172	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0007663	PMID:20451172	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0000505	OMIM:613464	TAS					P	HPO:probinson[2013-06-02]
OMIM:613464	Retinitis pigmentosa 51		HP:0000510	PMID:20451172	PCS		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0007843	PMID:20451172	PCS		4/4			P	HPO:probinson[2013-06-02];HPO:probinson[2023-03-11]
OMIM:613464	Retinitis pigmentosa 51		HP:0001513	PMID:20451172	PCS		0/4			P	HPO:probinson[2013-06-02];HPO:probinson[2023-03-11]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0002211	OMIM:601706	TAS					P	HPO:probinson[2015-07-19]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0000639	OMIM:601706	TAS					P	HPO:probinson[2009-02-17]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0007509	OMIM:601706	TAS					P	HPO:probinson[2009-02-17]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0000482	OMIM:601706	TAS					P	HPO:probinson[2009-02-17]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0000007	OMIM:601706	TAS					I	HPO:probinson[2009-02-17]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0000612	OMIM:601706	TAS					P	HPO:probinson[2009-02-17]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0007587	OMIM:601706	TAS					P	HPO:probinson[2015-07-19]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0000567	OMIM:601706	TAS					P	HPO:probinson[2015-07-19]
OMIM:601706	Yemenite deaf-blind hypopigmentation syndrome		HP:0008625	OMIM:601706	TAS					P	HPO:probinson[2009-02-17]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000286	PMID:33199684	PCS		11/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0030799	PMID:33199684	PCS		1/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000582	PMID:33199684	PCS		6/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000486	PMID:33199684	PCS		7/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000365	PMID:33199684	PCS		1/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001250	PMID:33199684	PCS		8/18			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001252	PMID:33199684	PCS		12/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0002020	PMID:33199684	PCS		7/19			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0003593	PMID:33199684	PCS					C	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0010863	PMID:33199684	PCS		13/13			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001270	PMID:33199684	PCS		21/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000718	PMID:33199684	PCS		4/17			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001647	PMID:33199684	PCS		1/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000219	PMID:33199684	PCS		11/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001643	PMID:33199684	PCS	HP:0003623	1/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001642	PMID:33199684	PCS		2/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001249	PMID:33199684	PCS		21/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000396	PMID:33199684	PCS		1/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000750	PMID:33199684	PCS		21/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0002793	PMID:33199684	PCS		5/19			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000431	PMID:33199684	PCS		3/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000194	PMID:33199684	PCS		9/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0011968	PMID:33199684	PCS	HP:0003623	12/19			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000490	PMID:33199684	PCS		9/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0010537	PMID:33199684	PCS		1/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000729	PMID:33199684	PCS		9/16			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000689	PMID:33199684	PCS		6/21			P	HPO:probinson[2021-02-28];HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000505	PMID:33199684	PCS		6/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0008589	PMID:33199684	PCS		4/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0004209	PMID:33199684	PCS		3/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0002007	PMID:33199684	PCS		9/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001357	PMID:33199684	PCS		5/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0007018	PMID:33199684	PCS		8/15			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001631	PMID:33199684	PCS		1/21			P	HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0000006	PMID:33199684	PCS					I	HPO:probinson[2021-02-28];HPO:probinson[2021-02-28]
OMIM:619149	Lessel-Kreienkamp syndrome		HP:0001655	PMID:33199684	PCS		3/21			P	HPO:probinson[2021-02-28]
OMIM:606069	Hemochromatosis, type 4		HP:0001397	PMID:11431687	PCS		3/11			P	HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0001394	PMID:11431687	PCS		1/11			P	HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0002240	PMID:11431687	PCS		5/20			P	HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0040270	OMIM:606069	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606069	Hemochromatosis, type 4		HP:0011675	PMID:11431687	PCS		1/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0003281	OMIM:606069	TAS		6/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0012378	PMID:11431687	PCS		2/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0000819	PMID:11431687	PCS		1/20			P	HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0012463	PMID:11431687	PCS		3/20			P	HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0002829	PMID:11431687	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0000518	OMIM:606069	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606069	Hemochromatosis, type 4		HP:0001903	OMIM:606069	IEA					P	HPO:skoehler[2019-09-07]
OMIM:606069	Hemochromatosis, type 4		HP:0000953	PMID:11431687	PCS		2/20			P	HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0001638	PMID:11431687	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0000802	OMIM:606069	TAS					P	HPO:skoehler[2017-07-13]
OMIM:606069	Hemochromatosis, type 4		HP:0002758	PMID:11431687	PCS		2/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0000006	PMID:11431687	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:606069	Hemochromatosis, type 4		HP:0001952	OMIM:606069	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618257	Deafness, autosomal recessive 112		HP:0000407	PMID:24312468	PCS		4/4			P	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:618257	Deafness, autosomal recessive 112		HP:0011463	PMID:24312468	PCS		4/4			C	HPO:probinson[2022-10-01]
OMIM:618257	Deafness, autosomal recessive 112		HP:0000007	PMID:24312468	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-01]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0030799	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0004325	PMID:27476655	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0003016	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001176	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0003577	PMID:27476655	PCS		4/4			C	HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000483	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000486	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000046	PMID:27476655	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0008905	PMID:27476655	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0006429	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0004322	PMID:27476655	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001250	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001272	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0002066	OMIM:617164	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0002020	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001251	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001270	OMIM:617164	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001629	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001508	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000518	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0011220	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000717	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0002979	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000218	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0006610	OMIM:617164	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000278	OMIM:617164	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001249	PMID:27476655	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000054	PMID:27476655	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000252	PMID:27476655	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000494	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000175	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0002870	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0002673	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001382	PMID:27476655	PCS		3/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0011968	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001263	PMID:27476655	PCS		2/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0004691	OMIM:617164	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000808	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000601	PMID:27476655	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0003712	PMID:27476655	PCS		1/4			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0001511	PMID:27476655	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0005616	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000545	PMID:27476655	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000347	PMID:27476655	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000028	PMID:27476655	PCS		1/2			P	HPO:probinson[2022-11-06]
OMIM:617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay		HP:0000006	PMID:27476655	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-06]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0007737	PMID:30850397	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0003577	PMID:32811249	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0003621	PMID:30850397	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000054	PMID:10053027	PCS		2/2	MALE		P	HPO:probinson[2020-12-10]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000750	PMID:30850397	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0001256	PMID:32811249;PMID:30850397	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000662	PMID:32811249;PMID:30850397	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0001156	PMID:10053027;PMID:32811249	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-10];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0003241	OMIM:615983	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0100259	PMID:32811249;PMID:30850397	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000668	PMID:30850397	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000007	PMID:10053027	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-10]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0007663	PMID:10053027;PMID:32811249;PMID:30850397	PCS		9/9			P	HPO:probinson[2020-12-10];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0004209	PMID:32811249	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0007401	PMID:30850397	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0007754	PMID:10053027	PCS		1/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-10]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000543	PMID:30850397	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0007787	PMID:30850397	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000510	PMID:10053027;PMID:30850397	PCS		5/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-10];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0001159	PMID:10053027	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-10]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0007843	PMID:30850397	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0000135	PMID:30850397	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-05-11]
OMIM:615983	Bardet-Biedl syndrome 5		HP:0001513	PMID:10053027;PMID:30850397	PCS		7/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-10];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:151430	B-CELL CLL/LYMPHOMA 2		HP:0001442	OMIM:151430	TAS					I	HPO:probinson[2009-02-17]
OMIM:151430	B-CELL CLL/LYMPHOMA 2		HP:0012191	OMIM:151430	TAS					P	HPO:probinson[2013-12-15]
OMIM:151430	B-CELL CLL/LYMPHOMA 2		HP:0012539	OMIM:151430	TAS					P	HPO:probinson[2013-12-15]
OMIM:619161	Carpal tunnel syndrome 2		HP:0033660	PMID:32686688	PCS		14/14			P	HPO:probinson[2021-04-16]
OMIM:619161	Carpal tunnel syndrome 2		HP:0012185	PMID:32686688	PCS		14/14			P	HPO:probinson[2021-02-27]
OMIM:619161	Carpal tunnel syndrome 2		HP:0033673	PMID:32686688	PCS		14/14			P	HPO:probinson[2021-04-16]
OMIM:619161	Carpal tunnel syndrome 2		HP:0033672	PMID:32686688	PCS		13/14			P	HPO:probinson[2021-04-16]
OMIM:619161	Carpal tunnel syndrome 2		HP:0003393	PMID:32686688	PCS		13/14			P	HPO:probinson[2021-02-27]
OMIM:619161	Carpal tunnel syndrome 2		HP:0046505	PMID:32686688	PCS		13/14		HP:0025301	P	HPO:probinson[2021-02-27]
OMIM:619161	Carpal tunnel syndrome 2		HP:0000006	PMID:32686688	PCS					I	HPO:probinson[2021-02-27];HPO:probinson[2021-02-27]
OMIM:222300	Wolfram syndrome 1		HP:0000365	PMID:9817917	PCS		9/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:222300	Wolfram syndrome 1		HP:0001250	PMID:16151413;PMID:9817917	PCS		1/20			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0001251	PMID:9817917	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-27]
OMIM:222300	Wolfram syndrome 1		HP:0000580	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000819	PMID:16151413;PMID:9817917	PCS		20/20			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0000518	PMID:16151413	PCS		5/10			P	HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0000639	OMIM:222300	IEA		2/10			P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0011463	PMID:16151413	PCS		5/10			C	HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0001889	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0001924	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000873	PMID:16151413;PMID:9817917	PCS		8/20			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0001249	PMID:16151413;PMID:9817917	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0006217	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000011	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0002059	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0002015	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0003621	PMID:16151413	PCS		5/10			C	HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0001260	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000072	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000708	OMIM:222300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:222300	Wolfram syndrome 1		HP:0000407	PMID:16151413	PCS		6/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0000508	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000007	OMIM:222300	IEA					I	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000821	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000029	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0001638	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0000648	PMID:16151413	PCS	HP:0003621	10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0000648	PMID:9817917	PCS		9/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:222300	Wolfram syndrome 1		HP:0001510	PMID:16151413	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-24]
OMIM:222300	Wolfram syndrome 1		HP:0001873	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0002401	OMIM:222300	IEA					P	HPO:iea[2009-02-17]
OMIM:222300	Wolfram syndrome 1		HP:0001337	OMIM:222300;PMID:9817917	PCS		10/20			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:222300	Wolfram syndrome 1		HP:0000126	OMIM:222300	IEA		8/10			P	HPO:iea[2009-02-17]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001276	PMID:36256512	PCS		12/14			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001298	PMID:36256512;PMID:32747156;PMID:25758857	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002169	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0033748	PMID:25758857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0000486	PMID:36256512	PCS		2/8			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002066	PMID:36256512;PMID:32747156	PCS		0/16			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0012706	PMID:25758857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001252	PMID:36256512	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0012707	PMID:25758857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0012708	PMID:25758857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0003593	PMID:36256512	PCS		9/19			C	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002061	PMID:36256512	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002280	PMID:36256512;PMID:32747156;PMID:25758857	PCS		9/17			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0000639	PMID:36256512	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0007020	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0010550	PMID:36256512	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0011463	PMID:36256512;PMID:32747156;PMID:25758857	PCS		12/21			C	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002878	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001945	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002359	PMID:36256512	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001348	PMID:36256512;PMID:25758857	PCS		17/18			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0003128	PMID:36256512;PMID:32747156;PMID:25758857	PCS		2/20			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001941	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002510	PMID:25758857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001762	PMID:36256512;PMID:32747156;PMID:25758857	PCS		2/21			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002133	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002650	PMID:25758857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0031936	PMID:36256512	PCS		8/8			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002376	PMID:36256512;PMID:32747156;PMID:25758857	PCS		15/21			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0003487	PMID:36256512;PMID:25758857	PCS		2/18			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002079	PMID:36256512;PMID:32747156;PMID:25758857	PCS		9/17			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001288	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002197	PMID:36256512	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001263	PMID:36256512;PMID:32747156;PMID:25758857	PCS		7/11			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0011449	PMID:36256512;PMID:25758857	PCS		7/17			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0011448	PMID:36256512;PMID:25758857	PCS		5/17			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0011096	PMID:36256512;PMID:32747156;PMID:25758857	PCS		1/17			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0034295	PMID:36256512;PMID:32747156;PMID:25758857	PCS		8/16			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0007371	PMID:25758857	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0000508	PMID:36256512	PCS		1/7			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0009830	PMID:36256512;PMID:32747156;PMID:25758857	PCS		2/21			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0000007	PMID:36256512	PCS					I	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0000648	PMID:36256512	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0002505	PMID:32747156	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0001258	PMID:36256512;PMID:25758857	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:620938	Spastic paraplegia 93, autosomal recessive		HP:0000544	PMID:36256512	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-01-08]
OMIM:610623	Cataract 11, multiple types		HP:0001276	OMIM:610623	IEA					P	HPO:skoehler[2019-02-22]
OMIM:610623	Cataract 11, multiple types		HP:0003577	PMID:9620774	PCS		2/2			C	HPO:probinson[2022-10-09]
OMIM:610623	Cataract 11, multiple types		HP:0000518	OMIM:610623	IEA					P	HPO:skoehler[2015-01-27]
OMIM:610623	Cataract 11, multiple types		HP:0000618	OMIM:610623	IEA					P	HPO:skoehler[2019-02-22]
OMIM:610623	Cataract 11, multiple types		HP:0000519	PMID:9620774	PCS	HP:0003577	2/2			P	HPO:probinson[2022-10-09]
OMIM:610623	Cataract 11, multiple types		HP:0002072	OMIM:610623	IEA					P	HPO:skoehler[2019-02-22]
OMIM:610623	Cataract 11, multiple types		HP:0000568	OMIM:610623	IEA					P	HPO:skoehler[2015-12-30]
OMIM:610623	Cataract 11, multiple types		HP:0000007	OMIM:610623	IEA					I	HPO:skoehler[2019-02-22]
OMIM:610623	Cataract 11, multiple types		HP:0000006	PMID:9620774	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-09]
OMIM:610623	Cataract 11, multiple types		HP:0001315	OMIM:610623	IEA					P	HPO:skoehler[2019-02-22]
OMIM:610623	Cataract 11, multiple types		HP:0001249	OMIM:610623	IEA					P	HPO:skoehler[2019-02-22]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0003577	OMIM:600430	IEA					C	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000582	PMID:20691407	PCS		4/6			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0004322	OMIM:600430	IEA					P	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000463	PMID:20691407	PCS		4/6			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001250	PMID:20691407	PCS		2/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000581	OMIM:600430	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000283	PMID:20691407	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0010049	OMIM:600430	IEA					P	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0011675	OMIM:600430	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000280	OMIM:600430	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001270	PMID:20691407	PCS		6/7			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0007021	OMIM:600430	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000718	PMID:20691407	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000733	PMID:20691407	PCS		3/3			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0012171	PMID:20691407	PCS		1/6			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000455	PMID:20691407	PCS		5/6			P	HPO:skoehler[2013-06-12];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000752	OMIM:600430	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000311	OMIM:600430	IEA					P	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001249	OMIM:600430	IEA					P	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0009803	OMIM:600430	IEA					P	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0002553	OMIM:600430	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001265	OMIM:600430	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001682	PMID:20691407	PCS		1/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000750	PMID:20691407	PCS		7/7			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0005863	PMID:20691407	PCS		5/6			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001442	OMIM:600430	IEA					I	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0011968	PMID:20691407	PCS		1/6			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000490	OMIM:600430	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001263	PMID:20691407	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000272	PMID:20691407	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0045025	OMIM:600430	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0011800	PMID:20691407	PCS		5/6			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0005280	OMIM:600430	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0012166	PMID:20691407	PCS		2/6			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000407	OMIM:600430	TAS		HP:0040283			P	HPO:skoehler[2014-05-04]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000729	PMID:20691407	PCS		1/6			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000964	OMIM:600430	IEA					P	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000821	PMID:20691407	PCS		2/7			P	HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0100716	PMID:20691407	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000006	PMID:20691407	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000248	PMID:20691407	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001513	PMID:20691407	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-08]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0001831	OMIM:600430	IEA					P	HPO:iea[2009-02-17]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0000445	OMIM:600430	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600430	Chromosome 2q37 deletion syndrome		HP:0004689	PMID:20691407	PCS		4/6			P	HPO:probinson[2023-06-08]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000286	PMID:36067766	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000341	PMID:36067766	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000582	PMID:36067766	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000252	PMID:36067766	PCS		2/5			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0001250	PMID:36067766	PCS		1/5			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0001263	PMID:36067766	PCS		5/5			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0003593	PMID:36067766	PCS		5/5			C	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0011523	PMID:36067766	PCS		1/5			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000639	PMID:36067766	PCS		3/5			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000407	PMID:36067766	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000729	PMID:36067766	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000508	PMID:36067766	PCS		2/5			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0007750	PMID:36067766	PCS		1/5			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000648	PMID:36067766	PCS		1/5			P	HPO:probinson[2022-12-04]
OMIM:620086	Intellectual developmental disorder with ocular anomalies and distinctive facial features		HP:0000006	PMID:36067766	PCS					I	HPO:probinson[2022-12-04]
OMIM:600356	Pachydermodactyly, familial		HP:0000924	OMIM:600356	IEA					P	HPO:iea[2009-02-17]
OMIM:600356	Pachydermodactyly, familial		HP:0000006	OMIM:600356	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0000486	OMIM:193003	IEA					P	HPO:iea[2009-02-17]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0000640	PMID:19471976	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0001761	PMID:19471976	PCS		3/17			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0002310	PMID:16211615	PCS		8/14			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0001272	PMID:16211615	PCS		2/9			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0002495	PMID:16211615	PCS		9/14			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0002066	PMID:16211615	PCS		11/14			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0001260	PMID:16211615	PCS		11/14			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0003680	OMIM:193003	IEA					C	HPO:iea[2009-02-17]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0002174	PMID:16211615	PCS					P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0011477	OMIM:193003	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0002070	PMID:16211615	PCS		12/14			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0000716	PMID:12489043	PCS		2/14			P	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0011463	PMID:12489043	PCS					C	HPO:probinson[2022-11-24]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0007670	OMIM:193003	IEA					P	HPO:probinson[2012-04-01]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0007772	OMIM:193003	IEA					P	HPO:probinson[2012-04-01]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0007179	OMIM:193003	IEA					P	HPO:iea[2009-02-17]
OMIM:193003	Nystagmus 4, congenital, autosomal dominant		HP:0000006	PMID:16211615	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-24]
OMIM:616534	Thyroid cancer, nonmedullary, 4		HP:0002895	PMID:25381600	PCS		3/4			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:616534	Thyroid cancer, nonmedullary, 4		HP:0100615	PMID:25381600	PCS		1/4			P	HPO:probinson[2022-10-11]
OMIM:616534	Thyroid cancer, nonmedullary, 4		HP:0002671	PMID:25381600	PCS		1/4			P	HPO:probinson[2022-10-11]
OMIM:616534	Thyroid cancer, nonmedullary, 4		HP:0012125	PMID:25381600	PCS		1/4			P	HPO:probinson[2022-10-11]
OMIM:616534	Thyroid cancer, nonmedullary, 4		HP:0000006	PMID:25381600	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-11]
OMIM:616534	Thyroid cancer, nonmedullary, 4		HP:0000853	OMIM:616534	IEA					P	HPO:skoehler[2018-10-08]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0001696	PMID:33139725	PCS		4/4			P	HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0001651	PMID:25469542	PCS		1/2			P	HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0003363	PMID:25469542	PCS		2/2			P	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0003251	PMID:33139725	PCS		1/1			P	HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0033036	PMID:33139725;PMID:25469542	PCS		1/6			P	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0000007	PMID:33139725	PCS					I	HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0000403	PMID:33139725	PCS		2/2			P	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0012735	PMID:33139725	PCS		1/1		HP:0011010	P	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:619607	Heterotaxy, visceral, 10, autosomal, with male infertility		HP:0011109	PMID:33139725	PCS		3/3			P	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0002465	OMIM:602541	TAS					P	HPO:skoehler[2013-01-22]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0003236	PMID:21665002	PCS		15/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0010628	OMIM:602541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0000252	PMID:21665002	PCS		6/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0000750	PMID:21665002	PCS		15/15			P	HPO:skoehler[2013-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0003198	OMIM:602541	TAS					P	HPO:skoehler[2013-01-22]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0001250	PMID:21665002	PCS		3/15			P	HPO:skoehler[2013-01-22];HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0003560	PMID:21665002	PCS		15/15			P	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0003593	PMID:21665002	PCS		15/15			C	HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0033686	PMID:21665002	PCS		15/15			P	HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0001290	PMID:21665002	PCS	HP:0003593	15/15			P	HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0001270	PMID:21665002	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0003391	OMIM:602541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0100297	PMID:21665002	PCS		15/15			P	HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0008064	OMIM:602541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0000007	PMID:21665002	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-04]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0002515	OMIM:602541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0001324	PMID:21665002	PCS	HP:0003593	15/15			P	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0001249	PMID:21665002	PCS		15/15			P	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0003677	OMIM:602541	TAS					C	HPO:skoehler[2012-10-17]
OMIM:602541	Muscular dystrophy, congenital, megaconial type		HP:0001644	PMID:21665002	PCS		6/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-06-04]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0001056	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0003577	OMIM:226600	TAS					C	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0033803	PMID:8513326	PCS		2/2			P	HPO:probinson[2022-04-18]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0001596	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0002860	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0002043	OMIM:226600	TAS					P	HPO:probinson[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0001371	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0001030	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0002164	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0000160	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0001075	PMID:8513326	PCS	HP:0003593	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0003593	PMID:8513326	PCS		2/2			C	HPO:probinson[2022-04-18]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0000518	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0001903	OMIM:226600	TAS					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0006297	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0000559	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0002019	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0002015	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0005203	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0004057	OMIM:226600	TAS					P	HPO:probinson[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0002031	OMIM:226600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0004395	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0008066	PMID:8513326	PCS	HP:0003593	2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-04-18]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0000509	OMIM:226600	IEA					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0000007	PMID:8513326	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-18]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0008404	OMIM:226600	TAS					P	HPO:skoehler[2013-05-03]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0001510	OMIM:226600	TAS					P	HPO:iea[2009-02-17]
OMIM:226600	Epidermolysis bullosa dystrophica, autosomal recessive		HP:0200097	PMID:8513326	PCS		2/2			P	HPO:probinson[2022-04-18]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0002069	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0002487	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0002188	PMID:12743223	PCS		2/37			P	HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0002123	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001272	PMID:12743223	PCS		3/37			P	HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001250	PMID:12743223	PCS		27/62			P	HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0002121	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0410053	OMIM:271980	TAS					P	HP:probinson[2019-06-12]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001252	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:6000991	PMID:9683595	PCS					P	HPO:probinson[2024-08-03]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001251	PMID:12743223	PCS		28/62			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0003593	PMID:12743223	PCS		1/14			C	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0032530	OMIM:271980	TAS					P	HP:probinson[2019-06-12]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001290	PMID:12743223	PCS		49/62			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0032531	OMIM:271980	TAS					P	HP:probinson[2019-06-12]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0032532	OMIM:271980	TAS					P	HP:probinson[2019-06-12]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001270	PMID:12743223	PCS		49/62			P	HPO:skoehler[2010-06-18];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000738	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0011463	PMID:12743223	PCS		7/14			C	HPO:probinson[2020-09-19];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000718	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0011462	PMID:12743223	PCS		1/14			C	HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000739	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000717	OMIM:271980	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000752	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001249	PMID:12743223	PCS		47/62			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001265	PMID:12743223	PCS		26/62			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0032528	OMIM:271980	TAS					P	HP:probinson[2019-06-12]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0003621	PMID:12743223	PCS		5/14			C	HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000750	PMID:12743223	PCS		50/62			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0002353	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0002133	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000496	OMIM:271980	IEA					P	HPO:iea[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0001263	OMIM:271980	TAS		20/20			P	HPO:skoehler[2019-02-22];HPO:skoehler[2014-04-04]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000709	OMIM:271980	TAS					P	HPO:probinson[2009-02-17]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000708	PMID:12743223	PCS		28/62			P	HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:6000608	PMID:12127325	PCS					P	HPO:probinson[2024-05-09]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0000007	PMID:12743223	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-19]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0100716	OMIM:271980	TAS					P	HPO:skoehler[2013-05-31]
OMIM:271980	Succinic semialdehyde dehydrogenase deficiency		HP:0500253	OMIM:271980	TAS					P	HP:probinson[2019-06-12]
OMIM:614323	Nevoid hypermelanosis, linear and whorled		HP:0001880	OMIM:614323	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614323	Nevoid hypermelanosis, linear and whorled		HP:0007572	OMIM:614323	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614323	Nevoid hypermelanosis, linear and whorled		HP:0003593	OMIM:614323	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614323	Nevoid hypermelanosis, linear and whorled		HP:0003745	OMIM:614323	TAS					I	HPO:skoehler[2015-12-30]
OMIM:614323	Nevoid hypermelanosis, linear and whorled		HP:0000006	OMIM:614323	TAS					I	HPO:skoehler[2012-10-17]
OMIM:191600	Ureter, cancer of		HP:0100516	OMIM:191600	IEA					P	HPO:skoehler[2015-08-05]
OMIM:191600	Ureter, cancer of		HP:0000006	OMIM:191600	IEA					I	HPO:iea[2009-02-17]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000286	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0010804	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0003196	PMID:19833603	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001252	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000319	PMID:19833603	PCS		3/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000316	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0100807	PMID:19833603	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0009623	PMID:19833603	PCS		5/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0003745	PMID:19833603	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000358	PMID:19833603	PCS		3/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001007	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0004635	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000297	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000331	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000490	PMID:19833603	PCS		3/24			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0011926	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000691	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001263	PMID:19833603	PCS		9/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000294	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0011800	PMID:19833603	PCS		2/12			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001182	PMID:19833603	PCS		2/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0012385	PMID:19833603	PCS		4/12			P	HPO:skoehler[2013-10-22];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0002827	PMID:19833603	PCS		1/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000729	PMID:19833603	PCS		2/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000767	PMID:19833603	PCS		2/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001852	PMID:19833603	PCS		4/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000400	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0009778	PMID:19833603	PCS		4/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000960	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000369	PMID:19833603	PCS		6/24			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000006	PMID:19833603	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0002786	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000445	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000341	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000582	PMID:19833603	PCS		7/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000384	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0003577	PMID:19833603	PCS		12/12			C	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000343	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000463	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000023	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001629	PMID:19833603	PCS		2/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0008551	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000579	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000414	PMID:19833603	PCS		2/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0006970	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000219	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000537	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000411	PMID:19833603	PCS		5/12			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000154	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000396	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000431	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001245	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0002057	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001761	PMID:19833603	PCS		1/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000276	PMID:19833603	PCS		1/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000193	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000470	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0045025	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0005280	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001838	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000508	PMID:19833603	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001636	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000307	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000664	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000268	PMID:19833603	PCS		1/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000465	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0007018	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001631	PMID:19833603	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000347	PMID:19833603	PCS		2/12			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0000028	PMID:19833603	PCS		2/7			P	HPO:probinson[2022-10-30]
OMIM:613458	Chromosome 16p13.3 duplication syndrome		HP:0001831	PMID:19833603	PCS		2/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-30]
OMIM:614337	Colorectal cancer, hereditary nonpolyposis, type 4		HP:0006716	OMIM:614337	TAS					P	HPO:probinson[2013-08-10]
OMIM:614337	Colorectal cancer, hereditary nonpolyposis, type 4		HP:0100615	OMIM:614337	TAS					P	HPO:probinson[2013-08-10]
OMIM:614337	Colorectal cancer, hereditary nonpolyposis, type 4		HP:0012114	OMIM:614337	TAS					P	HPO:probinson[2013-08-10]
OMIM:614337	Colorectal cancer, hereditary nonpolyposis, type 4		HP:0000006	OMIM:614337	TAS					I	HPO:probinson[2013-08-10]
OMIM:158400	Muscle cramps, familial		HP:0003445	OMIM:158400	TAS					P	HPO:probinson[2012-04-26]
OMIM:158400	Muscle cramps, familial		HP:0003236	OMIM:158400	TAS					P	HPO:probinson[2012-04-26]
OMIM:158400	Muscle cramps, familial		HP:0003394	OMIM:158400	TAS					P	HPO:probinson[2012-04-26]
OMIM:158400	Muscle cramps, familial		HP:0000006	OMIM:158400	TAS					I	HPO:probinson[2012-04-26]
OMIM:619613	Delayed puberty, self-limited		HP:0000044	PMID:32493844	PCS		0/6			P	HPO:probinson[2022-02-03]
OMIM:619613	Delayed puberty, self-limited		HP:0002750	PMID:32493844	PCS					P	HPO:probinson[2022-02-03]
OMIM:619613	Delayed puberty, self-limited		HP:0030344	PMID:32493844	PCS					P	HPO:probinson[2022-02-03]
OMIM:619613	Delayed puberty, self-limited		HP:0030341	PMID:32493844	PCS					P	HPO:probinson[2022-02-03]
OMIM:619613	Delayed puberty, self-limited		HP:0040171	PMID:32493844	PCS			MALE		P	HPO:probinson[2022-02-03]
OMIM:619613	Delayed puberty, self-limited		HP:0000823	PMID:32493844	PCS					P	HPO:probinson[2022-02-03]
OMIM:619613	Delayed puberty, self-limited		HP:0000006	PMID:32493844	PCS					I	HPO:probinson[2022-02-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0001531	PMID:31783057	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0002155	PMID:31783057	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0033331	PMID:31783057	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0002240	PMID:31783057	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0000007	PMID:31783057	PCS					I	HPO:probinson[2021-04-03];HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0000988	PMID:31783057	PCS	HP:0003623	1/1			P	HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0001945	PMID:31783057	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0001744	PMID:31783057	PCS		1/1			P	HPO:probinson[2021-04-03]
OMIM:619175	Proteasome-associated autoinflammatory syndrome 5		HP:0003623	PMID:31783057	PCS		1/1			C	HPO:probinson[2021-04-03]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003202	PMID:26208961	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003236	PMID:26208961	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0010628	PMID:26208961	TAS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003376	PMID:26208961	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003487	PMID:26208961	PCS		0/2			P	HPO:probinson[2019-12-22];HPO:probinson[2024-03-15]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003691	PMID:26208961	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0031237	PMID:26208961	PCS		2/2			P	HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0009027	PMID:26208961	PCS	HP:0003581	4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003805	PMID:26208961	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003438	PMID:26208961	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0020203	PMID:26208961	PCS					P	HPO:probinson[2020-03-14]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0000006	PMID:26208961	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003458	PMID:26208961	PCS		3/3			P	HPO:probinson[2019-12-22]
OMIM:617158	Myopathy, distal, with rimmed vacuoles		HP:0003557	PMID:26208961	PCS					P	HPO:probinson[2019-12-22]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0009053	PMID:18313024	PCS					P	HPO:probinson[2013-04-04]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0001288	OMIM:612020	TAS					P	HPO:skoehler[2014-03-24]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0003487	OMIM:612020	TAS					P	HPO:skoehler[2014-03-24]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0007020	PMID:18313024	PCS					P	HPO:probinson[2013-04-04]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0003693	PMID:18313024	PCS					P	HPO:probinson[2013-04-04]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0006827	PMID:18313024	PCS					P	HPO:probinson[2013-04-07]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0001272	OMIM:612020	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0001251	OMIM:612020	TAS		HP:0040283			P	HPO:skoehler[2014-03-24]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0000007	PMID:18313024	PCS					I	HPO:probinson[2013-01-09]
OMIM:612020	Spastic paraplegia 39, autosomal recessive		HP:0001347	OMIM:612020	TAS					P	HPO:skoehler[2014-03-24]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0001276	PMID:21337604	PCS		7/8			P	HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0003236	PMID:21337604	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0002063	PMID:21337604	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0003560	PMID:21337604	PCS					P	HPO:skoehler[2013-05-29];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0003593	PMID:21337604	PCS		7/8			C	HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0002093	PMID:21337604	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0000007	PMID:21337604	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0002878	PMID:21337604	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0001522	PMID:21337604	PCS		7/8			C	HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0002104	PMID:21337604	PCS		1/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0001612	PMID:21337604	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0003678	PMID:21337604	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-22]
OMIM:613869	Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related		HP:0003623	PMID:21337604	PCS		1/8			C	HPO:probinson[2023-02-22]
OMIM:208700	Ataxia with myoclonic epilepsy and presenile dementia		HP:0002123	OMIM:208700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:208700	Ataxia with myoclonic epilepsy and presenile dementia		HP:0001250	OMIM:208700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:208700	Ataxia with myoclonic epilepsy and presenile dementia		HP:0000726	OMIM:208700	IEA					P	HPO:iea[2009-02-17]
OMIM:208700	Ataxia with myoclonic epilepsy and presenile dementia		HP:0001271	OMIM:208700	IEA					P	HPO:iea[2009-02-17]
OMIM:208700	Ataxia with myoclonic epilepsy and presenile dementia		HP:0001251	OMIM:208700	IEA					P	HPO:iea[2009-02-17]
OMIM:208700	Ataxia with myoclonic epilepsy and presenile dementia		HP:0000007	OMIM:208700	IEA					I	HPO:iea[2009-02-17]
OMIM:208700	Ataxia with myoclonic epilepsy and presenile dementia		HP:0001336	OMIM:208700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0000286	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0004313	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0003577	OMIM:616911	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0004432	PMID:26216346	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-15]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0002719	PMID:26216346	PCS		3/4			P	HPO:probinson[2017-06-26];HPO:probinson[2024-03-15]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0001263	OMIM:616911	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0000316	OMIM:616911	PCS					P	HPO:probinson[2017-06-26]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0000007	PMID:26216346	IEA					I	HPO:probinson[2017-06-26]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0001270	PMID:26216346	PCS		4/6			P	HPO:probinson[2017-06-26];HPO:probinson[2024-03-15]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0002846	PMID:26216346	PCS		0/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2024-03-15]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0005280	PMID:26216346	PCS					P	HPO:probinson[2017-06-26]
OMIM:616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4		HP:0001249	PMID:26216346	PCS		3/4			P	HPO:probinson[2017-06-26]
OMIM:203655	Alopecia universalis congenita		HP:0002289	PMID:9445480	PCS	HP:0003623	11/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:203655	Alopecia universalis congenita		HP:0002223	PMID:9445480	PCS		11/11			P	HPO:probinson[2022-07-16]
OMIM:203655	Alopecia universalis congenita		HP:0000561	PMID:9445480	PCS		11/11			P	HPO:probinson[2022-07-16]
OMIM:203655	Alopecia universalis congenita		HP:0002221	PMID:9445480	PCS		11/11			P	HPO:probinson[2022-07-16]
OMIM:203655	Alopecia universalis congenita		HP:0000007	PMID:9445480	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-07-16]
OMIM:203655	Alopecia universalis congenita		HP:0002555	PMID:9445480	PCS		11/11			P	HPO:probinson[2022-07-16]
OMIM:203655	Alopecia universalis congenita		HP:0003623	PMID:9445480	PCS		11/11			C	HPO:probinson[2022-07-16]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0004322	PMID:31438591	PCS		18/22			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001772	PMID:31438591	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000160	PMID:31438591	PCS		10/19			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001252	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001290	PMID:31438591	PCS		6/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001090	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0011220	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002616	PMID:31438591	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001647	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000316	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000238	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000878	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002857	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001840	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001763	PMID:31438591	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002974	PMID:31438591	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000175	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000494	PMID:31438591	PCS		7/10			P	HPO:skoehler[2012-11-20];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000574	OMIM:245600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002750	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001222	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001382	PMID:31438591	PCS		10/18			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0004298	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000691	OMIM:245600	TAS					P	HPO:skoehler[2014-08-24]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0005021	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0011800	PMID:31438591	PCS		19/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0003083	PMID:31438591	PCS		3/5			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002827	OMIM:245600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000926	PMID:31438591	PCS		1/19			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000646	OMIM:245600	TAS					P	HPO:skoehler[2014-08-24]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000007	PMID:31438591	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000768	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0005616	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000565	OMIM:245600	TAS					P	HPO:skoehler[2014-08-24]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001852	PMID:31438591	PCS		6/13			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002987	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0003834	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000520	PMID:31438591	PCS		7/9			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000248	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000369	PMID:31438591	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001655	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0003015	PMID:31438591	PCS		3/5			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0008905	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000343	PMID:31438591	PCS		4/4			P	HPO:probinson[2020-08-08];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000540	PMID:31438591	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000023	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002162	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0003051	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0040160	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001270	PMID:31438591	PCS		5/5			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0012368	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000939	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0012095	PMID:31438591	PCS		20/24			P	HPO:skoehler[2015-01-27];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0009880	OMIM:245600	TAS					P	HPO:skoehler[2012-11-21]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0008593	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000938	PMID:31438591	PCS	HP:0011463	11/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0006099	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0008551	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001822	PMID:31438591	PCS		9/12			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000337	PMID:31438591	PCS		3/5			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002757	PMID:31438591	PCS		8/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000774	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000776	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000974	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0004976	PMID:31438591	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000973	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000274	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001363	PMID:31438591	PCS	HP:0003577	7/10			P	HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002650	PMID:31438591	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001762	PMID:31438591	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001640	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000592	PMID:31438591	PCS		8/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001087	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000470	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0005280	PMID:31438591	PCS		13/24			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000308	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001712	OMIM:245600	IEA					P	HPO:iea[2009-02-17]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0002007	PMID:31438591	PCS		6/16			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001631	PMID:31438591	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000465	PMID:31438591	PCS		8/14			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-08-08]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0000347	OMIM:245600	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects		HP:0001634	OMIM:245600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0007957	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000483	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0003236	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000486	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000365	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0004322	PMID:33523931	PCS		7/10			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001772	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001250	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001252	PMID:33523931	PCS		7/9			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0025024	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000280	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000081	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0006191	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000639	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000316	PMID:33523931	PCS		5/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001642	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000278	PMID:33523931	PCS		4/9			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001007	PMID:33523931	PCS		8/20			P	HPO:probinson[2021-05-05];HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001249	PMID:33523931	PCS		7/7			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000358	PMID:33523931	PCS		3/7			P	HPO:probinson[2021-05-05];HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0009748	PMID:33523931	PCS		1/7			P	HPO:probinson[2021-05-05];HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000252	PMID:33523931	PCS		5/10			P	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000494	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000054	PMID:33523931	PCS		5/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0002079	PMID:33523931	PCS		3/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0002673	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001263	PMID:33523931	PCS		10/10			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0011800	PMID:33523931	PCS		6/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0010557	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000609	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001419	PMID:33523931	PCS					I	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0011330	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000729	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0003316	PMID:33523931	PCS		3/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000047	PMID:33523931	PCS		5/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000369	PMID:33523931	PCS		4/7			P	HPO:probinson[2021-05-05];HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000126	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0003577	PMID:33523931	PCS		10/10			C	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001792	PMID:33523931	PCS		2/9			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000540	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001274	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0002283	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0002240	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001629	PMID:33523931	PCS		6/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0100702	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0008872	PMID:33523931	PCS		4/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0002119	PMID:33523931	PCS		8/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0100507	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0004935	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000256	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0005989	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0002910	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001561	PMID:33523931	PCS	HP:0011461	5/9			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001363	PMID:33523931	PCS		3/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000076	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001762	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001321	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001882	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001162	PMID:33523931	PCS		3/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0005162	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001838	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001518	PMID:33523931	PCS		7/9			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000506	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001719	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000668	PMID:33523931	PCS		3/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0002804	PMID:33523931	PCS		1/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000307	PMID:33523931	PCS		1/9			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001511	PMID:33523931	PCS	HP:0011461	8/10			P	HPO:probinson[2021-05-02]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001830	PMID:33523931	PCS		4/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0001873	PMID:33523931	PCS		2/10			P	HPO:probinson[2021-05-05]
OMIM:301056	Multiple congenital anomalies-neurodevelopmental syndrome, X-linked		HP:0000028	PMID:33523931	PCS		5/20			P	HPO:probinson[2021-05-05]
OMIM:614860	Dystonia 23		HP:0000473	OMIM:614860	TAS					P	HPO:skoehler[2012-11-16]
OMIM:614860	Dystonia 23		HP:0002356	OMIM:614860	TAS					P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0003676	OMIM:614860	TAS					C	HPO:skoehler[2015-12-30]
OMIM:614860	Dystonia 23		HP:0002530	OMIM:614860	TAS					P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0001288	OMIM:614860	TAS					P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0001272	OMIM:614860	TAS		HP:0040283			P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0002120	OMIM:614860	TAS		HP:0040283			P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0002451	OMIM:614860	TAS					P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0003581	OMIM:614860	TAS					C	HPO:skoehler[2012-11-16]
OMIM:614860	Dystonia 23		HP:0011675	OMIM:614860	TAS		HP:0040283			P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0001618	OMIM:614860	TAS					P	HPO:skoehler[2015-04-19]
OMIM:614860	Dystonia 23		HP:0000006	OMIM:614860	TAS					I	HPO:skoehler[2012-11-16]
OMIM:614860	Dystonia 23		HP:0002346	OMIM:614860	TAS		HP:0040282			P	HPO:skoehler[2012-11-28]
OMIM:614860	Dystonia 23		HP:0001336	OMIM:614860	TAS					P	HPO:skoehler[2015-04-19]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0001696	PMID:23040496	PCS		4/9			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0003251	PMID:23040496	PCS		2/3			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0003593	PMID:23040496	PCS		1/9			C	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0033036	PMID:23040496	PCS		9/9			P	HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0012208	OMIM:614874	TAS					P	HPO:probinson[2013-04-07]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0031565	PMID:23040496	PCS		1/9			P	HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0012257	PMID:23040496	PCS		9/9			P	HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0011108	PMID:23040496	PCS		8/9			P	HPO:skoehler[2012-11-20]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0200073	PMID:23040496	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0012265	PMID:23040496	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0012256	PMID:23040496	PCS		9/9			P	HPO:probinson[2013-04-07]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0012384	PMID:23040496	PCS		8/9		HP:0031796	P	HPO:skoehler[2013-10-22]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0012263	PMID:23040496	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0000007	PMID:23040496	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0000403	PMID:23040496	PCS		1/9			P	HPO:skoehler[2012-11-20];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0002643	PMID:23040496	PCS		8/9			P	HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0004469	PMID:23040496	PCS		3/9			P	HPO:skoehler[2012-11-16];HPO:probinson[2023-02-12]
OMIM:614874	Ciliary dyskinesia, primary, 18		HP:0003623	PMID:23040496	PCS		8/9			C	HPO:probinson[2023-02-12]
OMIM:618096	Premature ovarian failure 15		HP:0003621	PMID:29231814	PCS		2/2			C	HPO:probinson[2023-02-22]
OMIM:618096	Premature ovarian failure 15		HP:0000869	PMID:29231814	PCS		1/2			P	HPO:probinson[2023-02-22]
OMIM:618096	Premature ovarian failure 15		HP:0000858	PMID:29231814	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:618096	Premature ovarian failure 15		HP:0008232	PMID:29231814	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:618096	Premature ovarian failure 15		HP:0000876	PMID:29231814	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618096	Premature ovarian failure 15		HP:0000007	PMID:29231814	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:618096	Premature ovarian failure 15		HP:0031103	PMID:29231814	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000044	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0003577	PMID:1594017	PCS		1/2			C	HPO:probinson[2022-05-26]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000046	PMID:1594017	PCS		1/2			P	HPO:probinson[2022-05-26]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000122	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0001251	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0003593	PMID:1594017	PCS		1/2			C	HPO:probinson[2022-05-26]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000458	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000218	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0008734	OMIM:308700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000054	PMID:1594017	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-26]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0001341	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000771	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0001761	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0030344	PMID:18160472;OMIM:308700	PCS		20/20			P	HPO:probinson[2017-08-12];HPO:probinson[2015-06-02]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0003782	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0030341	PMID:18160472;OMIM:308700	PCS		20/20			P	HPO:probinson[2017-08-12];HPO:probinson[2015-06-02]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0003164	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0040171	PMID:1594017	PCS		2/2			P	HPO:probinson[2022-05-26]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0002929	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0001419	PMID:1594017	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-26]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0004409	OMIM:308700	IEA					P	HPO:skoehler[2019-09-07]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000029	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0001335	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000028	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0002225	OMIM:308700	IEA					P	HPO:iea[2009-02-17]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000027	OMIM:308700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:308700	Hypogonadotropic hypogonadism 1 with or without anosmia		HP:0000324	OMIM:308700	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0001276	OMIM:176500	IEA					P	HPO:iea[2009-02-17]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0002344	OMIM:176500	IEA					P	HPO:iea[2009-02-17]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0011970	OMIM:176500	TAS					P	HPO:skoehler[2015-01-21]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0000726	OMIM:176500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0002063	OMIM:176500	TAS					P	HPO:skoehler[2009-02-17]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0001257	OMIM:176500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0000006	OMIM:176500	IEA					I	HPO:iea[2009-02-17]
OMIM:176500	Cerebral amyloid angiopathy, itm2b-related, 1		HP:0001337	OMIM:176500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0003596	PMID:36657711	PCS		5/8			C	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0011462	PMID:36657711	PCS		3/8			C	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0011706	PMID:36657711	PCS		3/8			P	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0006682	PMID:36657711	PCS		2/8			P	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0001635	PMID:36657711	PCS		3/8			P	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0012664	PMID:36657711	PCS		8/8			P	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0001631	PMID:36657711	PCS		2/8			P	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0000006	PMID:36657711	PCS					I	HPO:probinson[2023-06-12]
OMIM:620247	Cardiomyopathy, dilated, 1OO		HP:0001644	PMID:36657711	PCS		8/8			P	HPO:probinson[2023-06-12]
OMIM:309350	Melnick-Needles syndrome		HP:0002982	OMIM:309350	TAS					P	HPO:probinson[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0003015	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000486	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000684	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000882	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001377	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0005792	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0011335	OMIM:309350	TAS					P	HPO:probinson[2012-04-30]
OMIM:309350	Melnick-Needles syndrome		HP:0001270	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001508	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001609	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0010230	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0009882	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000316	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0003826	OMIM:309350	TAS					C	HPO:probinson[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001704	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0002857	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000774	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001423	OMIM:309350	IEA					I	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000894	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001763	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000336	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0002751	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0004611	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000175	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000274	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000472	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000692	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0005446	OMIM:309350	TAS					P	HPO:probinson[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001762	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001288	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0002673	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000270	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000071	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0002092	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0009771	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0002827	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000767	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000403	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001539	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0002208	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000400	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0002205	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000520	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0001634	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:309350	Melnick-Needles syndrome		HP:0000347	OMIM:309350	TAS					P	HPO:probinson[2012-04-30]
OMIM:309350	Melnick-Needles syndrome		HP:0000126	OMIM:309350	IEA					P	HPO:iea[2009-02-17]
OMIM:613855	Episodic ataxia, type 5		HP:0002069	PMID:10762541	PCS		3/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0003621	PMID:10762541	PCS		4/7			C	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0000640	PMID:10762541	PCS		1/9			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0002078	PMID:10762541	PCS		1/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0002321	PMID:10762541	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0002131	PMID:10762541	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0002373	PMID:10762541	PCS		2/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0001260	PMID:10762541	PCS		3/9			P	HPO:probinson[2013-08-10];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0001251	PMID:10762541	PCS		1/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0002172	PMID:10762541	PCS		3/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0010850	PMID:10762541	PCS		1/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0011147	PMID:10762541	PCS		2/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0012000	PMID:10762541	PCS		1/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0007270	PMID:10762541	PCS		1/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0011462	PMID:10762541	PCS		3/7			C	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0003829	PMID:10762541	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0000006	PMID:10762541	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2022-03-26]
OMIM:613855	Episodic ataxia, type 5		HP:0001336	PMID:10762541	PCS		1/9			P	HPO:probinson[2022-03-26];HPO:probinson[2022-03-26]
OMIM:173450	Platelet factor 3 deficiency		HP:0001892	OMIM:173450	IEA					P	HPO:iea[2009-02-17]
OMIM:173450	Platelet factor 3 deficiency		HP:0000006	OMIM:173450	IEA					I	HPO:iea[2009-02-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0010805	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000582	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000343	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0001156	OMIM:614684	IEA					P	HPO:skoehler[2015-01-19]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000316	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000219	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0030084	OMIM:614684	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0001500	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0006610	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000377	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0009789	OMIM:614684	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0009803	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000396	OMIM:614684	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000154	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000054	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000574	OMIM:614684	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000431	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0001999	OMIM:614684	IEA					P	HPO:skoehler[2015-01-19]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000767	OMIM:614684	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000349	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000007	PMID:19938075	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2025-09-26]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000768	OMIM:614684	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0001698	OMIM:614684	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0200055	OMIM:614684	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614684	Hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, impaired intellectual development, and recurrent inflammatory episodes		HP:0000028	OMIM:614684	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0003510	PMID:7923357	PCS					P	HPO:iea[2015-03-21]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0008905	OMIM:264180	IEA					P	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0003311	OMIM:264180	IEA					P	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000463	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0001508	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0002719	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000319	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0002938	OMIM:264180	IEA					P	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0001945	OMIM:264180	TAS					P	HPO:skoehler[2013-04-18]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0001762	OMIM:264180	IEA					P	HPO:skoehler[2010-06-20]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0002650	OMIM:264180	IEA					P	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0003042	OMIM:264180	TAS					P	HPO:probinson[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000592	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000272	OMIM:264180	IEA					P	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000470	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0005680	OMIM:264180	IEA					P	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0011800	OMIM:264180	TAS					P	HPO:skoehler[2013-11-28]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0012385	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000926	OMIM:264180	IEA					P	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0006243	OMIM:264180	TAS					P	HPO:probinson[2015-03-21]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000007	OMIM:264180	IEA					I	HPO:iea[2009-02-17]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0002007	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000465	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000347	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:264180	Pseudodiastrophic dysplasia		HP:0000248	OMIM:264180	TAS					P	HPO:skoehler[2017-07-13]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000582	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0003577	PMID:34112922	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0002188	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0002002	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0001252	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0003593	PMID:36747105	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0010544	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0008551	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000954	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0001763	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000278	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000577	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0003623	PMID:37134193	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000252	PMID:34112922;PMID:36747105	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000574	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0002079	PMID:34112922;PMID:36747105;PMID:37134193	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0002373	PMID:34112922;PMID:36747105;PMID:37134193	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0002395	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0001263	PMID:34112922;PMID:36747105;PMID:37134193	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0002072	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0005280	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000729	PMID:34112922;PMID:36747105;PMID:37134193	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000508	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000369	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000303	PMID:34112922;PMID:36747105;PMID:37134193	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620535	Developmental delay, dysmorphic facies, and brain anomalies		HP:0000006	PMID:34112922	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:112910	Brachydactyly, type A6		HP:0003027	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0003038	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0004322	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0003022	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0005013	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0009370	OMIM:112910	TAS					P	HPO:probinson[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0000925	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0001837	OMIM:112910	TAS					P	HPO:probinson[2012-06-08]
OMIM:112910	Brachydactyly, type A6		HP:0009466	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0006135	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0008127	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0009843	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0008368	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0009702	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0001500	OMIM:112910	TAS					P	HPO:probinson[2012-06-03]
OMIM:112910	Brachydactyly, type A6		HP:0005736	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0000006	OMIM:112910	IEA					I	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0002984	OMIM:112910	IEA					P	HPO:iea[2009-02-17]
OMIM:112910	Brachydactyly, type A6		HP:0009803	OMIM:112910	TAS					P	HPO:probinson[2012-06-03]
OMIM:112910	Brachydactyly, type A6		HP:0001831	OMIM:112910	TAS					P	HPO:probinson[2012-06-08]
OMIM:616939	Chorea, childhood-onset, with psychomotor retardation		HP:0002465	PMID:27123486	PCS					P	HPO:probinson[2017-06-25]
OMIM:616939	Chorea, childhood-onset, with psychomotor retardation		HP:0001263	PMID:27123486	PCS					P	HPO:probinson[2017-06-25]
OMIM:616939	Chorea, childhood-onset, with psychomotor retardation		HP:0002072	PMID:27123486	PCS					P	HPO:probinson[2017-06-25]
OMIM:616939	Chorea, childhood-onset, with psychomotor retardation		HP:0000007	PMID:27123486	PCS					I	HPO:probinson[2017-06-25]
OMIM:616939	Chorea, childhood-onset, with psychomotor retardation		HP:0004305	PMID:27123486	PCS					P	HPO:probinson[2017-06-25]
OMIM:616939	Chorea, childhood-onset, with psychomotor retardation		HP:0001249	OMIM:616939	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616939	Chorea, childhood-onset, with psychomotor retardation		HP:0002457	PMID:27123486	PCS					P	HPO:probinson[2017-06-25]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0003577	PMID:25090642	PCS		3/29			C	HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0003621	PMID:25090642	PCS		13/29			C	HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0009917	PMID:25090642	PCS		3/29			P	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0000541	PMID:25090642	PCS		3/29			P	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0003596	PMID:25090642	PCS		1/29			C	HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0000518	PMID:25090642	PCS		24/29			P	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0011463	PMID:25090642	PCS		4/29			C	HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0011462	PMID:25090642	PCS		8/29			C	HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0000006	PMID:25090642	PCS					I	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620253	Cataract 50 with or without glaucoma		HP:0000501	PMID:25090642	PCS		15/29			P	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:300406	FG syndrome 3		HP:0002213	PMID:12239712	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0003577	PMID:12239712	PCS		6/6			C	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0011968	PMID:12239712	PCS		3/4			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0002021	PMID:12239712	PCS		0/3			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0001252	PMID:12239712	PCS	HP:0003623	5/5			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0001274	PMID:12239712	PCS		1/6			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0004482	PMID:12239712	PCS		4/4			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0008070	PMID:12239712	PCS		2/2			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0011304	PMID:12239712	PCS		4/4			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0034392	PMID:12239712	PCS		2/3			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0010055	PMID:12239712	PCS		4/4			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0000407	PMID:12239712	PCS		0/3			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0011220	PMID:12239712	PCS		5/5			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0007099	PMID:12239712	PCS		1/6			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0012450	PMID:12239712	PCS		3/3			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0001417	PMID:12239712	PCS					I	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0001522	PMID:12239712	PCS		2/6			C	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0000752	PMID:12239712	PCS		3/3			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0001249	PMID:12239712	PCS		6/6			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0002236	PMID:12239712	PCS		3/3			P	HPO:probinson[2023-07-07]
OMIM:300406	FG syndrome 3		HP:0000028	PMID:12239712	PCS		1/4			P	HPO:probinson[2023-07-07]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001276	PMID:31402090	PCS		2/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000486	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001156	PMID:31402090	PCS		2/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000089	PMID:31402090	PCS		1/7		HP:0012834	P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000023	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001290	PMID:31402090	PCS		2/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001270	PMID:31402090	PCS		6/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0009183	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000718	PMID:31402090	PCS		2/6			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000733	PMID:31402090	PCS		1/6			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000378	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000278	PMID:31402090	PCS		3/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001642	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001249	PMID:31402090	PCS		6/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0006956	PMID:31402090	PCS		2/5			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001245	PMID:31402090	PCS		2/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000750	PMID:31402090	PCS		5/6			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0002079	PMID:31402090	PCS		2/5			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0031717	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0004691	PMID:31402090	PCS		2/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0100021	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0100710	PMID:31402090	PCS		1/6			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0009274	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000729	PMID:31402090	PCS		3/6			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001537	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000568	PMID:31402090	PCS		1/7		HP:0012833	P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0100719	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0100716	PMID:31402090	PCS		2/6			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001852	PMID:31402090	PCS		2/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000465	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000006	PMID:31402090	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000347	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000303	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0000545	PMID:31402090	PCS		2/7		HP:0012825	P	HPO:probinson[2020-08-13]
OMIM:618914	Neurodevelopmental, jaw, eye, and digital syndrome		HP:0001655	PMID:31402090	PCS		1/7			P	HPO:probinson[2020-08-13]
OMIM:606519	PHACE association		HP:0005314	OMIM:606519	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606519	PHACE association		HP:0001250	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0100545	OMIM:606519	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606519	PHACE association		HP:0100029	OMIM:606519	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606519	PHACE association		HP:0001629	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0000519	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0007486	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0002617	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0001305	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0001423	OMIM:606519	TAS					I	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0001643	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0000851	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0003745	OMIM:606519	TAS					I	HPO:skoehler[2015-12-30]
OMIM:606519	PHACE association		HP:0007986	OMIM:606519	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606519	PHACE association		HP:0002277	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0001321	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0002076	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0410264	OMIM:606519	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606519	PHACE association		HP:0001263	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0001680	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0000609	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0000568	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:606519	PHACE association		HP:0000648	OMIM:606519	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606519	PHACE association		HP:0000329	OMIM:606519	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606519	PHACE association		HP:0007434	OMIM:606519	TAS					P	HPO:skoehler[2012-10-17]
OMIM:606519	PHACE association		HP:0004942	OMIM:606519	TAS					P	HPO:probinson[2012-05-05]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0003577	PMID:31570889	PCS					C	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000483	PMID:31570889	PCS		1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000486	PMID:31570889	PCS		2/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0001156	PMID:31570889	PCS		2/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0009918	PMID:31570889	PCS		1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000639	PMID:31570889	PCS	HP:0003577	1/7		HP:0012832	P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000518	PMID:31570889	PCS	HP:0003577	2/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0010055	PMID:31570889	PCS		2/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0006297	PMID:31570889	PCS		1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0007663	PMID:31570889	PCS					P	HPO:probinson[2020-04-23];HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0030084	PMID:31570889	PCS		2/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0006335	PMID:31570889	PCS		1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000677	PMID:31570889	PCS		2/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0001249	PMID:31570889	PCS		0/7			P	HPO:probinson[2020-04-23];HPO:probinson[2024-03-16]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000698	PMID:31570889	PCS		3/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0007946	PMID:31570889	PCS		1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000431	PMID:31570889	PCS		3/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0009928	PMID:31570889	PCS		3/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0001442	PMID:31570889	PCS					I	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0004552	PMID:31570889	PCS		3/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000691	PMID:31570889	PCS		3/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0001263	PMID:31570889	PCS		0/7			P	HPO:probinson[2020-04-23];HPO:probinson[2024-03-16]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000272	PMID:31570889	PCS		4/7		HP:0012833	P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0011332	PMID:31570889	PCS		4/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000568	PMID:31570889	PCS		1/7		HP:0012833	P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000689	PMID:31570889	PCS		1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000648	PMID:31570889	PCS		1/7		HP:0012833	P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0001852	PMID:31570889	PCS		1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0009779	PMID:31570889	PCS		1/7		HP:0012833	P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000545	PMID:31570889	PCS		4/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000501	PMID:31570889	PCS	HP:0003577	1/7			P	HPO:probinson[2020-04-23]
OMIM:618727	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic		HP:0000324	PMID:31570889	PCS		7/7			P	HPO:probinson[2020-04-23];HPO:probinson[2020-04-23]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0000750	PMID:20970105	PCS		1/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0003487	PMID:20970105	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0031936	PMID:20970105	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0002497	PMID:20970105	PCS					P	HPO:skoehler[2015-01-26];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0001260	PMID:20970105	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0002066	PMID:20970105	PCS		6/6			P	HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0200049	PMID:20970105	PCS		2/6			P	HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0003593	PMID:20970105	PCS		6/6			C	HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0002070	PMID:20970105	PCS		4/6			P	HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0009072	PMID:20970105	PCS		4/6			P	HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0007083	PMID:20970105	PCS		5/6			P	HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0000639	PMID:20970105	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0000712	PMID:20970105	PCS		4/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0000007	PMID:20970105	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0000648	PMID:20970105	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0006895	PMID:20970105	PCS		4/6			P	HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0003677	PMID:20970105	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:613672	Spastic ataxia 4, autosomal recessive		HP:0002313	PMID:20970105	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-20]
OMIM:238600	Type I hyperlipoproteinemia		HP:0000660	OMIM:238600	IEA					P	HPO:iea[2009-02-17]
OMIM:238600	Type I hyperlipoproteinemia		HP:0001013	PMID:16174715	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:238600	Type I hyperlipoproteinemia		HP:0002013	OMIM:238600	TAS					P	HPO:skoehler[2010-06-18]
OMIM:238600	Type I hyperlipoproteinemia		HP:0002574	OMIM:238600	IEA					P	HPO:iea[2009-02-17]
OMIM:238600	Type I hyperlipoproteinemia		HP:0003124	PMID:16174715	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:238600	Type I hyperlipoproteinemia		HP:0003077	OMIM:238600	IEA					P	HPO:iea[2009-02-17]
OMIM:238600	Type I hyperlipoproteinemia		HP:0031028	PMID:16174715	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-08]
OMIM:238600	Type I hyperlipoproteinemia		HP:0012238	OMIM:238600	TAS					P	HPO:skoehler[2013-04-02]
OMIM:238600	Type I hyperlipoproteinemia		HP:0011462	PMID:16174715	PCS		1/1			C	HPO:probinson[2024-03-08]
OMIM:238600	Type I hyperlipoproteinemia		HP:0001735	PMID:16174715	PCS		1/1			P	HPO:probinson[2024-03-08]
OMIM:238600	Type I hyperlipoproteinemia		HP:0000007	PMID:16174715	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:238600	Type I hyperlipoproteinemia		HP:0002018	OMIM:238600	TAS					P	HPO:skoehler[2009-02-17]
OMIM:238600	Type I hyperlipoproteinemia		HP:0001433	OMIM:238600	IEA					P	HPO:iea[2009-02-17]
OMIM:238600	Type I hyperlipoproteinemia		HP:0004416	PMID:16174715	PCS		0/1			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-08]
OMIM:238600	Type I hyperlipoproteinemia		HP:0000952	OMIM:238600	IEA					P	HPO:iea[2009-02-17]
OMIM:238600	Type I hyperlipoproteinemia		HP:0001744	OMIM:238600	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615565	Retinitis pigmentosa 67		HP:0000007	PMID:24043777	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-10]
OMIM:615565	Retinitis pigmentosa 67		HP:0000510	PMID:24043777	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-02-10]
OMIM:271200	Spinal muscular atrophy, Ryukyuan type		HP:0002751	OMIM:271200	IEA					P	HPO:iea[2009-02-17]
OMIM:271200	Spinal muscular atrophy, Ryukyuan type		HP:0001761	OMIM:271200	IEA					P	HPO:iea[2009-02-17]
OMIM:271200	Spinal muscular atrophy, Ryukyuan type		HP:0003593	OMIM:271200	IEA					C	HPO:iea[2009-02-17]
OMIM:271200	Spinal muscular atrophy, Ryukyuan type		HP:0002380	OMIM:271200	IEA					P	HPO:iea[2009-02-17]
OMIM:271200	Spinal muscular atrophy, Ryukyuan type		HP:0000007	OMIM:271200	IEA					I	HPO:iea[2009-02-17]
OMIM:271200	Spinal muscular atrophy, Ryukyuan type		HP:0007269	OMIM:271200	IEA					P	HPO:iea[2009-02-17]
OMIM:271200	Spinal muscular atrophy, Ryukyuan type		HP:0007126	OMIM:271200	IEA					P	HPO:iea[2009-02-17]
OMIM:102530	Spermatogenic failure 6		HP:0003251	PMID:17847006	PCS		3/3	MALE		P	HPO:probinson[2020-04-27];HPO:probinson[2020-04-27]
OMIM:102530	Spermatogenic failure 6		HP:0000007	PMID:17847006	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-04-27]
OMIM:102530	Spermatogenic failure 6		HP:0031136	PMID:17847006	PCS					P	HPO:probinson[2020-04-27]
OMIM:102530	Spermatogenic failure 6		HP:0012205	PMID:17847006	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2020-04-27]
OMIM:301095	Intellectual developmental disorder, X-linked 110		HP:0002067	PMID:34184986	PCS		1/3			P	HPO:probinson[2023-04-10]
OMIM:301095	Intellectual developmental disorder, X-linked 110		HP:0001344	PMID:34184986	PCS		1/3			P	HPO:probinson[2023-04-10]
OMIM:301095	Intellectual developmental disorder, X-linked 110		HP:0001419	PMID:34184986	PCS					I	HPO:probinson[2023-04-10]
OMIM:301095	Intellectual developmental disorder, X-linked 110		HP:0011463	PMID:34184986	PCS		3/3			C	HPO:probinson[2023-04-10]
OMIM:301095	Intellectual developmental disorder, X-linked 110		HP:0002572	PMID:34184986	PCS		1/3			P	HPO:probinson[2023-04-10]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0002663	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0006108	OMIM:611717	TAS					P	HPO:probinson[2013-04-13]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000582	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000343	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0001498	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0001773	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000463	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0005257	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0001156	OMIM:611717	TAS					P	HPO:skoehler[2014-11-26]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0001371	OMIM:611717	PCS				HP:0012825	P	HPO:probinson[2012-03-02]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000581	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0010049	OMIM:611717	TAS					P	HPO:probinson[2013-04-13]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0004580	OMIM:611717	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000280	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0010585	OMIM:611717	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0006192	OMIM:611717	TAS					P	HPO:probinson[2013-04-13]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0001609	OMIM:611717	TAS					P	HPO:probinson[2013-04-12]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0008551	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0008873	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0008897	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0007665	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000311	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000179	OMIM:611717	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0001620	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0006216	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000215	OMIM:611717	TAS					P	HPO:skoehler[2013-04-12]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0009803	OMIM:611717	TAS					P	HPO:probinson[2013-04-13]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0002655	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0004634	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000154	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0003026	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000431	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0004279	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000475	OMIM:611717	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0005069	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000272	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000470	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0011800	OMIM:611717	TAS					P	HPO:skoehler[2013-11-28]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0005280	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0002091	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000926	OMIM:611717	PCS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000767	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0002967	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0002866	OMIM:611717	IEA					P	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0000006	OMIM:611717	IEA					I	HPO:probinson[2009-02-17]
OMIM:611717	Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech		HP:0001831	OMIM:611717	TAS					P	HPO:probinson[2012-06-10]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000483	PMID:33867525	PCS		3/29			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000365	PMID:33867525	PCS		3/32			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000486	PMID:33867525	PCS		4/29			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001052	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001250	PMID:33867525	PCS		7/33			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000160	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001252	PMID:33867525	PCS		14/27			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0003593	PMID:25217958	PCS		4/4			C	HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0012745	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0002381	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0010055	PMID:25217958	PCS		2/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000718	PMID:33867525	PCS		7/34			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0010296	PMID:33867525	PCS		5/22			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0012471	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0002938	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000316	PMID:25217958	PCS		2/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000678	PMID:25217958	PCS		1/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0003307	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000752	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001007	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001249	PMID:33867525	PCS		23/30			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000494	PMID:25217958	PCS		1/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001385	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001344	PMID:25217958	PCS		2/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0002197	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000490	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001263	PMID:25217958	PCS		1/4			P	HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0010554	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000729	PMID:33867525	PCS		4/34			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001852	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000006	PMID:25217958	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000248	PMID:25217958	PCS		1/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000369	PMID:25217958	PCS		3/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000445	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001276	PMID:33867525	PCS		1/27			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000343	PMID:25217958	PCS		2/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000189	OMIM:616078	TAS					P	HPO:skoehler[2014-11-26]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000540	PMID:33867525	PCS		9/29			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001270	PMID:33867525	PCS		33/34			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0025161	PMID:33867525	PCS		8/34			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000739	PMID:33867525	PCS		8/34			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000219	PMID:25217958	PCS		1/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000218	PMID:25217958	PCS		3/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000750	PMID:25217958	PCS		33/34			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000276	PMID:25217958	PCS		1/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001761	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0002373	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000194	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000508	PMID:25217958	PCS		3/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000307	PMID:25217958	PCS		1/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0100716	PMID:33867525	PCS		3/34			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000505	PMID:33867525	PCS		14/29			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0002007	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000664	PMID:25217958	PCS		2/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0007018	PMID:33867525	PCS		6/34			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000028	PMID:33867525	PCS		3/13			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0000545	PMID:33867525	PCS		3/29			P	HPO:probinson[2022-07-01]
OMIM:616078	Intellectual developmental disorder, autosomal dominant 29		HP:0001513	PMID:25217958	PCS		1/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0002850	PMID:31874111	PCS		2/4			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0001342	PMID:35289316	PCS		3/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0004313	PMID:35289316	PCS		3/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0410300	PMID:31874111	PCS		1/4			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0003593	PMID:35289316	PCS		3/3			C	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0010976	PMID:31874111	PCS		4/4			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0012424	PMID:35289316	PCS		1/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0012121	PMID:35289316	PCS		1/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0012122	PMID:35289316;PMID:31874111	PCS		3/7			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0100653	PMID:35289316	PCS		1/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0001417	PMID:31874111	PCS					I	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0012490	PMID:35289316	PCS		3/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0001433	PMID:35289316	PCS		3/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0004315	PMID:31874111	PCS		3/4			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0002754	PMID:35289316	PCS		1/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0000698	PMID:35289316	PCS		1/3			P	HPO:probinson[2022-07-19]
OMIM:301081	Autoinflammatory disease, systemic, X-linked		HP:0001875	PMID:35289316	PCS		1/3			P	HPO:probinson[2022-07-19]
OMIM:263610	Polyhydramnios, chronic idiopathic		HP:0001561	OMIM:263610	TAS					P	HPO:probinson[2009-02-17]
OMIM:263610	Polyhydramnios, chronic idiopathic		HP:0000007	OMIM:263610	TAS					I	HPO:probinson[2015-04-18]
OMIM:231630	Glutamate monosodium sensitivity		HP:0031284	PMID:942671	PCS	HP:0003581				P	HPO:nvasilevsky[2018-06-13]
OMIM:231630	Glutamate monosodium sensitivity		HP:0002094	PMID:942671	PCS	HP:0003581				P	HPO:nvasilevsky[2018-06-13]
OMIM:231630	Glutamate monosodium sensitivity		HP:0000007	OMIM:231630	IEA					I	HPO:iea[2009-02-17]
OMIM:231630	Glutamate monosodium sensitivity		HP:0100749	PMID:942671	PCS	HP:0003581				P	HPO:nvasilevsky[2018-06-13]
OMIM:231630	Glutamate monosodium sensitivity		HP:0002018	OMIM:231630	IEA					P	HPO:iea[2009-02-17]
OMIM:231630	Glutamate monosodium sensitivity		HP:0002315	PMID:4117590	PCS					P	HPO:probinson[2009-02-17]
OMIM:231630	Glutamate monosodium sensitivity		HP:0001962	PMID:942671	PCS	HP:0003581				P	HPO:nvasilevsky[2018-06-13]
OMIM:613100	Glaucoma 1, open angle, O		HP:0012108	OMIM:613100	TAS					P	HPO:probinson[2013-06-02]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0001265	PMID:22065524	PCS		1/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0003477	PMID:22065524	PCS		3/4			P	HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0003676	PMID:22065524	PCS					C	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0003621	PMID:22065524	PCS		2/4			C	HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0001310	PMID:22065524	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0001272	PMID:22065524	PCS		3/3			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0003693	PMID:22065524	PCS		4/4			P	HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0001260	PMID:22065524	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0001284	PMID:22065524	PCS		3/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0001251	PMID:22065524	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0025708	PMID:22065524	PCS		2/4			C	HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0000639	PMID:22065524	PCS		3/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0000657	PMID:22065524	PCS		3/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0000514	PMID:22065524	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0006254	PMID:22065524	PCS		4/4			P	HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0000007	PMID:22065524	PCS					I	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0002936	PMID:22065524	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0002359	PMID:22065524	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-10-23]
OMIM:615217	Ataxia-Oculomotor apraxia 3		HP:0001324	PMID:22065524	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-23]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0012221	PMID:7738360	PCS		6/8			P	HPO:skoehler[2013-04-02];HPO:probinson[2023-01-28]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0003621	PMID:7738360	PCS		1/1			C	HPO:probinson[2023-01-28];HPO:probinson[2023-01-28]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0001075	PMID:7738360	PCS		7/8			P	HPO:probinson[2023-01-28]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0000007	OMIM:131850	TAS					I	HPO:skoehler[2017-07-13]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0000989	PMID:7738360	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-28]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0008404	PMID:7738360	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-28]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0000006	PMID:7738360	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-28]
OMIM:131850	Epidermolysis bullosa dystrophica, pretibial		HP:0000962	OMIM:131850	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0002421	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0000286	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0002069	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0007858	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0003236	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0007814	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0001274	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0001290	PMID:31256877	PCS		2/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0003390	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0012469	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0007182	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0007165	PMID:31256877	PCS					P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0000514	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0002317	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0002835	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0001249	PMID:31256877	PCS					P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0000358	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0020206	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0001762	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0005565	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0002098	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0001263	PMID:31256877	PCS		2/2			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0005562	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0001284	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0006380	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0000407	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0008981	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0007078	PMID:31256877	PCS					P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0001239	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0000762	PMID:31256877	PCS					P	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0003713	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0000006	PMID:31256877	PCS					I	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:618733	Neuromuscular disease and ocular or auditory anomalies with or without seizures		HP:0003458	PMID:31256877	PCS		1/4			P	HPO:probinson[2020-09-02]
OMIM:134900	Fibrinolytic defect		HP:0007420	OMIM:134900	IEA					P	HPO:iea[2009-02-17]
OMIM:134900	Fibrinolytic defect		HP:0000006	OMIM:134900	IEA					I	HPO:iea[2009-02-17]
OMIM:134900	Fibrinolytic defect		HP:0000974	OMIM:134900	IEA					P	HPO:iea[2009-02-17]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0002059	PMID:26697887;PMID:29764912	PCS		2/6			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0003236	PMID:29764912	IEA		1/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0001310	PMID:29764912	PCS		3/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0003542	PMID:29764912	PCS		1/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0001272	PMID:26697887;PMID:29764912	PCS		4/6			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0001263	PMID:29764912	PCS		8/8			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0002151	PMID:29764912	PCS		1/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0001251	PMID:29764912	PCS		3/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0030187	PMID:29764912	PCS		1/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0003593	PMID:29764912	PCS		2/4			C	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0011463	PMID:26697887;PMID:29764912	PCS		4/6			C	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0000007	PMID:26697887	PCS					I	HPO:probinson[2021-08-22];HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0000722	PMID:26697887	PCS		2/2			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0000725	PMID:26697887;PMID:29764912	PCS		4/6			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0002317	PMID:29764912	PCS		1/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0025435	PMID:29764912	PCS		1/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0001249	PMID:29764912	PCS		3/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0001348	PMID:29764912	PCS		1/4			P	HPO:probinson[2021-08-22]
OMIM:619405	Spinocerebellar ataxia, autosomal recessive 30		HP:0001337	PMID:29764912	PCS		1/4			P	HPO:probinson[2021-08-22]
OMIM:616736	Tremor, hereditary essential, 5		HP:0003621	PMID:26188006	PCS		7/21			C	HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0002067	PMID:26188006	PCS		0/15			P	HPO:probinson[2017-06-17];HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0003596	PMID:26188006	PCS		2/21			C	HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0031947	PMID:26188006	PCS		6/17			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0003584	PMID:26188006	PCS		1/21			C	HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0002174	PMID:26188006	PCS		18/18			P	HPO:probinson[2017-06-17];HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0002080	PMID:26188006	PCS		16/16			P	HPO:probinson[2017-06-17];HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0011463	PMID:26188006	PCS		1/21			C	HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0011462	PMID:26188006	PCS		11/21			C	HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0003829	PMID:26188006	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0030186	PMID:26188006	PCS		7/8			P	HPO:probinson[2017-06-17];HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0000006	PMID:26188006	PCS					I	HPO:probinson[2017-06-17]
OMIM:616736	Tremor, hereditary essential, 5		HP:0003831	PMID:26188006	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:616736	Tremor, hereditary essential, 5		HP:0003677	PMID:26188006	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-15]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0000541	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0001773	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0001156	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0003498	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0003375	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0005011	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0003173	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0006370	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0010231	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0010230	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0002938	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0006134	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0003745	OMIM:609616	IEA					I	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0001763	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0003026	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0003301	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0002650	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0003180	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0000407	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0001837	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0000926	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0000887	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0002866	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0001216	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:609616	Spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctatecalcifications, and deafness		HP:0004568	OMIM:609616	IEA					P	HPO:iea[2009-02-17]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0000121	PMID:9312167	PCS		13/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0003621	PMID:9312167	PCS					C	HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0008341	PMID:9312167	PCS					P	HPO:probinson[2022-03-12];HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0031033	PMID:9312167	PCS		17/17			P	HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0002749	PMID:9312167	PCS		1/18			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0002900	PMID:9312167	PCS		5/18			P	HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0002901	OMIM:179800	IEA					P	HPO:probinson[2009-02-17]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0001324	OMIM:179800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0002756	OMIM:179800	IEA					P	HPO:probinson[2009-02-17]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0000006	PMID:9312167	PCS					I	HPO:probinson[2013-03-12];HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0000787	PMID:9312167	PCS		10/18			P	HPO:probinson[2022-03-12]
OMIM:179800	Renal tubular acidosis, distal, autosomal dominant		HP:0003259	PMID:9312167	PCS		1/18			P	HPO:probinson[2022-03-12]
OMIM:620284	Deafness, autosomal dominant 89		HP:0003577	PMID:33111345	PCS					C	HPO:probinson[2023-06-25]
OMIM:620284	Deafness, autosomal dominant 89		HP:0000365	PMID:33111345	PCS					P	HPO:probinson[2023-06-25]
OMIM:620284	Deafness, autosomal dominant 89		HP:0011463	PMID:33111345	PCS					C	HPO:probinson[2023-06-25]
OMIM:620284	Deafness, autosomal dominant 89		HP:0000006	PMID:33111345	PCS					I	HPO:probinson[2023-06-25]
OMIM:147050	Ige responsiveness, atopic		HP:0003212	OMIM:147050	TAS					P	HPO:iea[2009-02-17]
OMIM:147050	Ige responsiveness, atopic		HP:0002099	OMIM:147050	IEA					P	HPO:iea[2009-02-17]
OMIM:147050	Ige responsiveness, atopic		HP:0000964	OMIM:147050	IEA					P	HPO:iea[2009-02-17]
OMIM:147050	Ige responsiveness, atopic		HP:0003193	OMIM:147050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:147050	Ige responsiveness, atopic		HP:0000006	OMIM:147050	IEA					I	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000286	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000243	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000160	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001252	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000316	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0003745	PMID:17853473	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001643	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000278	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001763	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000358	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001249	PMID:17853473	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0002553	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000054	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0030148	PMID:17853473	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000453	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001263	PMID:17853473	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0010511	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0011800	OMIM:158170	TAS					P	HPO:skoehler[2013-11-28]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001182	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0008080	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0002705	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001539	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001852	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000047	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000369	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000006	PMID:17853473	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000341	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000582	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0003577	PMID:17853473	PCS		1/1			C	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0011918	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000189	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000343	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001795	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000023	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0002002	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000463	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0002286	OMIM:158170	IEA					P	HPO:skoehler[2010-06-20]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0011313	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001629	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0011682	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000219	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000218	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0006610	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001028	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001864	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000395	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000431	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000233	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0002650	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000750	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0005882	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000592	PMID:17853473	PCS		1/1			P	HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000470	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000272	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0045025	PMID:17853473	PCS		1/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0005280	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0001631	PMID:17853473	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-13]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000545	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:158170	Chromosome 9P deletion syndrome		HP:0000347	OMIM:158170	IEA					P	HPO:iea[2009-02-17]
OMIM:606243	Alveolar soft part sarcoma		HP:0001442	OMIM:606243	TAS					I	HPO:probinson[2013-03-30]
OMIM:606243	Alveolar soft part sarcoma		HP:0012218	OMIM:606243	TAS					P	HPO:probinson[2013-01-09]
OMIM:619363	Angioedema, hereditary, 6		HP:0003596	PMID:31087670	PCS		2/6			C	HPO:probinson[2021-07-13]
OMIM:619363	Angioedema, hereditary, 6		HP:0100665	PMID:31087670	PCS		6/6			P	HPO:probinson[2021-07-13]
OMIM:619363	Angioedema, hereditary, 6		HP:0000282	PMID:31087670	PCS		5/6			P	HPO:probinson[2021-07-13]
OMIM:619363	Angioedema, hereditary, 6		HP:0011462	PMID:31087670	IEA		4/6			C	HPO:probinson[2021-07-13]
OMIM:619363	Angioedema, hereditary, 6		HP:0031244	PMID:31087670	PCS		5/6		HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619363	Angioedema, hereditary, 6		HP:0000006	PMID:31087670	TAS					I	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:619363	Angioedema, hereditary, 6		HP:0007514	PMID:31087670	PCS		2/6		HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0004322	PMID:25217960	PCS		2/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0004387	PMID:25217960	PCS	HP:0003593				P	HPO:skoehler[2015-01-27];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0025420	PMID:25217960	PCS		1/3			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0003073	PMID:25217960	PCS		2/3			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0012177	PMID:25217960	PCS		2/3			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001508	PMID:25217960	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001903	PMID:25217959	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0008872	PMID:25217959	PCS		1/1			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001945	PMID:25217959	PCS	HP:0011463	1/1		HP:0025303	P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0005208	PMID:25217960	PCS	HP:0003623	2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001744	PMID:25217960	PCS		2/3			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001744	PMID:25217959	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0003623	PMID:25217960	PCS		3/3			C	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0040218	PMID:25217960	PCS		2/3			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0003326	PMID:25217960	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001287	PMID:25217960	PCS		1/3			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001025	PMID:25217959	PCS		1/1			P	HPO:probinson[2020-10-11];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0005521	PMID:25217960	PCS		1/3		HP:0025303	P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0002572	PMID:25217960	PCS					P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0011900	PMID:25217960	IEA					P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0003281	PMID:25217959;PMID:25217960	PCS		4/4		HP:0025303	P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0012378	PMID:25217959	PCS		1/1		HP:0025303	P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0011227	PMID:25217959;PMID:25217960	PCS		4/4		HP:0025303	P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0002829	PMID:25217960	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0011473	PMID:25217960	PCS					P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001954	PMID:25217960	PCS		3/3			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0000988	PMID:25217960	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001873	PMID:25217959	IEA		1/1			P	HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0001876	PMID:25217960	PCS		1/3		HP:0025303	P	HPO:skoehler[2014-11-26];HPO:probinson[2020-10-11]
OMIM:616050	Autoinflammation with infantile enterocolitis		HP:0000006	PMID:25217959	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-10-11]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002960	PMID:23666743	TAS					P	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0003774	PMID:23666743	PCS		1/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0000100	PMID:23319571	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002783	PMID:23319571	PCS	HP:0003593	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001596	PMID:23666743	PCS		1/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0020072	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0003493	PMID:23319571	PCS	HP:0003621	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0003493	PMID:23666743	PCS		3/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0003493	PMID:26233237	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001890	PMID:23666743	PCS		1/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002240	PMID:23319571	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002240	PMID:23666743	PCS		2/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0030374	PMID:23319571	PCS	HP:0011463	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0030374	PMID:26233237	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0410293	PMID:23319571	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0010702	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0031964	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0033207	PMID:23319571	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0100721	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0012177	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002719	PMID:26233237	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002716	PMID:23319571	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002716	PMID:23666743	PCS		1/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002716	PMID:26233237	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001744	PMID:23319571	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001744	PMID:23666743	PCS		1/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001369	PMID:23666743	PCS		1/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0005404	PMID:23430113;PMID:26233237	PCS		2/2			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0003565	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0000010	PMID:23319571	PCS	HP:0003593	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0005523	PMID:23666743	PCS		2/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0031956	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0005421	PMID:23666743	PCS		2/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0030388	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0025475	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0045042	PMID:23666743	PCS		2/3			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0011108	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0012578	PMID:23319571	PCS	HP:0011463	1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0011227	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0031041	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002729	PMID:23319571	PCS	HP:0011463	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0000007	PMID:23319571	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0000403	PMID:23319571	PCS	HP:0003593	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0000403	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001954	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0020136	PMID:23319571	PCS	HP:0003621	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0008940	PMID:23430113	PCS		1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001973	PMID:23666743	PCS		1/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0002788	PMID:23319571	PCS	HP:0003593	1/1			P	HPO:probinson[2020-11-20]
OMIM:615559	Autoimmune lymphoproliferative syndrome, type III		HP:0001433	PMID:23430113;PMID:26233237	PCS		2/2			P	HPO:probinson[2020-11-20]
OMIM:604454	Welander distal myopathy		HP:0003376	PMID:23348830	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2023-05-20]
OMIM:604454	Welander distal myopathy		HP:0003693	PMID:23348830	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2023-05-20]
OMIM:604454	Welander distal myopathy		HP:0003581	PMID:23348830	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-05-20]
OMIM:604454	Welander distal myopathy		HP:0002460	PMID:23348830	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2023-05-20]
OMIM:604454	Welander distal myopathy		HP:0000007	OMIM:604454	TAS					I	HPO:skoehler[2013-05-03]
OMIM:604454	Welander distal myopathy		HP:0003805	PMID:23348830	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2023-05-20]
OMIM:604454	Welander distal myopathy		HP:0000006	PMID:23348830	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2023-05-20]
OMIM:604454	Welander distal myopathy		HP:0003677	PMID:23348830	PCS					C	HPO:skoehler[2013-05-03];HPO:probinson[2023-05-20]
OMIM:604454	Welander distal myopathy		HP:0008180	PMID:23348830	PCS					P	HPO:skoehler[2013-05-03];HPO:probinson[2023-05-20]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0010307	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001371	PMID:22522446	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001252	PMID:22522446	PCS		3/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0002020	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001290	PMID:22522446	PCS		2/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0012822	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0003093	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0010783	PMID:22522446	PCS		2/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0033031	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001629	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000975	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001649	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000218	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001945	PMID:22522446	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000559	PMID:22522446	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0002835	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001623	PMID:22522446	PCS		2/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001188	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001762	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000331	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000573	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001662	PMID:22522446	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000194	PMID:22522446	PCS		2/3			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0011968	PMID:22522446	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0002033	PMID:22522446	PCS					P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001284	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0012736	PMID:22522446	PCS		2/4			P	HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0034252	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000822	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000007	PMID:22522446	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001319	PMID:22522446	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0007610	PMID:22522446	PCS		2/3			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000763	PMID:22522446	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001511	PMID:22522446	PCS		1/3			P	HPO:probinson[2022-07-16];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0001510	OMIM:614653	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000369	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0002104	PMID:22522446	PCS		2/3			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0002643	PMID:22522446	PCS		2/3			P	HPO:probinson[2022-07-16]
OMIM:614653	Neuropathy, hereditary sensory and autonomic, type VI		HP:0000522	PMID:22522446	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0033309	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0002003	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001396	PMID:29429573	PCS		4/4			P	HPO:probinson[2021-08-18];HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0000365	PMID:29429573	PCS		4/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001395	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0012202	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001508	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001903	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001944	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0000238	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0002757	PMID:29429573	PCS		4/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001824	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0005208	PMID:29429573	PCS		4/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0410204	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0006579	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0005743	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001385	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0002572	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0002099	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0000592	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001263	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0012537	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0000093	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0033736	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0006580	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0011473	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0000007	PMID:29429573	PCS					I	HPO:probinson[2021-08-18];HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0002900	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0000989	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0001414	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0004349	PMID:29429573	PCS		2/4			P	HPO:probinson[2021-08-18]
OMIM:619377	Osteootohepatoenteric syndrome		HP:0002027	PMID:29429573	PCS		1/4			P	HPO:probinson[2021-08-18]
OMIM:616044	Deafness, autosomal dominant 65		HP:0001751	PMID:24729547	PCS		0/9			P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616044	Deafness, autosomal dominant 65		HP:0011462	PMID:24729547;PMID:24729539	PCS		19/19			C	HPO:probinson[2022-04-12];HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:616044	Deafness, autosomal dominant 65		HP:0001730	PMID:24729547;PMID:24729539	PCS	HP:0011462	19/19			P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12];HPO:probinson[2022-04-12]
OMIM:616044	Deafness, autosomal dominant 65		HP:0000006	PMID:24729539	PCS					I	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:616044	Deafness, autosomal dominant 65		HP:0003677	PMID:24729539	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-04-12]
OMIM:616722	Retinal dystrophy and iris coloboma with or without congenital cataract		HP:0011484	PMID:26056285	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-31]
OMIM:616722	Retinal dystrophy and iris coloboma with or without congenital cataract		HP:0000519	PMID:26056285	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-31]
OMIM:616722	Retinal dystrophy and iris coloboma with or without congenital cataract		HP:0007663	PMID:26056285	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-31]
OMIM:616722	Retinal dystrophy and iris coloboma with or without congenital cataract		HP:0000612	PMID:26056285	PCS	HP:0003577	6/9			P	HPO:probinson[2022-03-31]
OMIM:616722	Retinal dystrophy and iris coloboma with or without congenital cataract		HP:0000006	PMID:26056285	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-31]
OMIM:616722	Retinal dystrophy and iris coloboma with or without congenital cataract		HP:0001105	PMID:26056285	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-31]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0025144	OMIM:610353	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0000708	OMIM:610353	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0003621	PMID:16826524	PCS		8/10			C	HPO:probinson[2022-09-03]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0001289	OMIM:610353	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0001332	OMIM:610353	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0011463	PMID:16826524	PCS		1/10			C	HPO:probinson[2022-09-03]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0003829	OMIM:610353	IEA					I	HPO:skoehler[2018-10-08]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0012759	PMID:16826524	PCS		0/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-03]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0025710	PMID:16826524	PCS		1/10			C	HPO:probinson[2022-09-03]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0031951	PMID:16826524	PCS		10/10			P	HPO:probinson[2022-09-03]
OMIM:610353	Epilepsy, nocturnal frontal lobe, 4		HP:0000006	PMID:16826524	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-03]
OMIM:187260	Telangiectasia, hereditary benign		HP:0011463	PMID:14627680	PCS					C	HPO:probinson[2012-07-17]
OMIM:187260	Telangiectasia, hereditary benign		HP:0002617	OMIM:187260	IEA					P	HPO:skoehler[2018-10-08]
OMIM:187260	Telangiectasia, hereditary benign		HP:0007489	PMID:14627680	PCS					P	HPO:probinson[2009-02-17]
OMIM:187260	Telangiectasia, hereditary benign		HP:0000006	PMID:14627680	PCS					I	HPO:probinson[2009-02-17]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0003301	PMID:11565064	PCS					P	HPO:skoehler[2015-02-28];HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0005645	PMID:11565064	PCS		1/1			P	HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0003621	PMID:11565064	PCS					C	HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0003365	OMIM:614135	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0006407	PMID:11565064	PCS					P	HPO:probinson[2015-03-10]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0003370	PMID:11565064	PCS					P	HPO:probinson[2015-03-10]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0030839	PMID:11565064	IEA		2/2			P	HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0010585	PMID:11565064	PCS					P	HPO:skoehler[2015-02-28]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0002829	PMID:11565064	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0010582	PMID:11565064	PCS					P	HPO:skoehler[2015-02-28]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0002815	OMIM:614135	TAS					P	HPO:skoehler[2012-11-21]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0006398	PMID:11565064	PCS					P	HPO:probinson[2015-03-10]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0030041	PMID:11565064	PCS		1/2			P	HPO:skoehler[2014-10-10];HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0002758	PMID:11565064	PCS	HP:0003621	2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0000006	PMID:11565064	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-26]
OMIM:614135	Epiphyseal dysplasia, multiple, 6		HP:0002654	PMID:11565064	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-26]
OMIM:604326	Spinocerebellar ataxia 12		HP:0002345	OMIM:604326	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604326	Spinocerebellar ataxia 12		HP:0001300	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0000496	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0001310	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0002530	OMIM:604326	IEA					P	HPO:skoehler[2010-06-18]
OMIM:604326	Spinocerebellar ataxia 12		HP:0001272	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0002120	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0001260	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0002075	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0002073	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0000716	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0007141	OMIM:604326	IEA					P	HPO:skoehler[2010-06-20]
OMIM:604326	Spinocerebellar ataxia 12		HP:0000726	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0000739	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0000317	OMIM:604326	IEA					P	HPO:skoehler[2010-06-18]
OMIM:604326	Spinocerebellar ataxia 12		HP:0000746	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0000006	OMIM:604326	IEA					I	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0002346	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:604326	Spinocerebellar ataxia 12		HP:0001347	OMIM:604326	IEA					P	HPO:iea[2009-02-17]
OMIM:613882	Hypomagnesemia 6, renal		HP:0003621	PMID:21397062	PCS		2/3			C	HPO:probinson[2023-02-18]
OMIM:613882	Hypomagnesemia 6, renal		HP:0033759	PMID:21397062	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:613882	Hypomagnesemia 6, renal		HP:0002321	PMID:21397062	PCS		1/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-02-18]
OMIM:613882	Hypomagnesemia 6, renal		HP:0002917	PMID:21397062	PCS		4/4			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-18]
OMIM:613882	Hypomagnesemia 6, renal		HP:0011463	PMID:21397062	PCS		1/3			C	HPO:probinson[2023-02-18]
OMIM:613882	Hypomagnesemia 6, renal		HP:0001324	PMID:21397062	PCS		1/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-02-18]
OMIM:613882	Hypomagnesemia 6, renal		HP:0002315	PMID:21397062	PCS		1/4			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-02-18]
OMIM:613882	Hypomagnesemia 6, renal		HP:0000006	PMID:21397062	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0005632	OMIM:119100	IEA					P	HPO:iea[2009-02-17]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0010109	OMIM:119100	IEA					P	HPO:iea[2009-02-17]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0004058	OMIM:119100	TAS					P	HPO:probinson[2012-07-16]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0009460	OMIM:119100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0001839	OMIM:119100	TAS					P	HPO:probinson[2009-02-17]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0006495	OMIM:119100	IEA					P	HPO:iea[2009-02-17]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0006443	OMIM:119100	TAS					P	HPO:probinson[2009-02-17]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0001171	OMIM:119100	TAS					P	HPO:probinson[2012-07-16]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0009556	OMIM:119100	TAS					P	HPO:probinson[2012-07-16]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0000378	OMIM:119100	IEA					P	HPO:iea[2009-02-17]
OMIM:119100	Split-Hand/foot malformation with long bone deficiency 1		HP:0000006	OMIM:119100	IEA					I	HPO:iea[2009-02-17]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000341	PMID:31630790	PCS		3/10			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000582	PMID:31630790	PCS		2/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000340	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0003593	PMID:31630790	PCS					C	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0011182	PMID:31630790	PCS					P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000319	PMID:31630790	PCS		3/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0100704	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000414	PMID:31630790	PCS		2/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000219	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0002416	PMID:31630790	PCS		2/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000411	PMID:31630790	PCS		5/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0001302	PMID:31630790	PCS	HP:0003593	5/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0001348	PMID:31630790	PCS		1/2			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000253	PMID:31630790	PCS		4/4			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0008936	PMID:31630790	PCS		3/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000574	PMID:31630790	PCS		2/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0032409	PMID:31630790	PCS		2/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0002079	PMID:31630790	PCS		3/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0011800	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000327	PMID:31630790	PCS		2/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000007	PMID:31630790	PCS					I	HPO:probinson[2020-04-29];HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000648	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0000664	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0001257	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:618737	Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures		HP:0006304	PMID:31630790	PCS		1/5			P	HPO:probinson[2020-04-29]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003577	PMID:28190456	PCS		4/12			C	HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003236	PMID:28190456	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003676	OMIM:617404	TAS					C	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0000486	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0004322	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0001250	PMID:28190456	PCS		1/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0001252	PMID:28190456	PCS		11/12			P	HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003593	PMID:28190456	PCS		1/12			C	HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0002061	OMIM:617404	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0001270	PMID:28190456	PCS		11/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003391	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0000518	PMID:28190456	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0011463	PMID:28190456	PCS		7/12			C	HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0009126	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003307	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0007126	PMID:28190456	PCS					P	HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003701	PMID:28190456	PCS					P	HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0003306	PMID:28190456	PCS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0001249	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0000252	OMIM:617404	TAS		2/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0002650	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0001288	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0001263	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0002093	OMIM:617404	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0002808	PMID:28190456	PCS		2/12			P	HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0000007	PMID:28190456	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-27]
OMIM:617404	Muscular dystrophy, congenital, with cataracts and intellectual disability		HP:0030051	OMIM:617404	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0001397	PMID:18620775	PCS		17/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0001289	PMID:18620775	PCS		5/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0002155	PMID:10369257	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:6000785	PMID:18620775	PCS					P	HPO:probinson[2024-06-29]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0025630	PMID:10369257	PCS					P	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0003581	PMID:10369257	PCS					C	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0001395	PMID:10369257	PCS		11/14			P	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0011966	PMID:10369257	PCS		37/37			P	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0030948	PMID:10369257	PCS		15/19			P	HPO:probinson[2021-10-14];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0002181	PMID:10369257	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0031964	PMID:10369257	PCS		17/19			P	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0033193	PMID:10369257	PCS		4/14			P	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0500153	PMID:10369257	PCS					P	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0033196	PMID:10369257	PCS		6/14			P	HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0000007	PMID:10369257	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0001987	PMID:18620775	PCS		14/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0001733	PMID:10369257	PCS		5/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0001259	PMID:18620775	PCS		3/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:603471	Citrullinemia, type II, adult-onset		HP:0001402	PMID:10369257	PCS		1/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-10-14]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003676	OMIM:613662	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003434	PMID:12825077	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0000365	OMIM:613662	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0004389	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0002024	OMIM:613662	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001250	OMIM:613662	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001252	OMIM:613662	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001251	OMIM:613662	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003593	OMIM:613662	TAS					C	HPO:skoehler[2012-11-21]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001290	OMIM:613662	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003270	OMIM:613662	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0009141	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001824	OMIM:613662	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0002579	OMIM:613662	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001324	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0002019	OMIM:613662	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003688	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003689	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003324	OMIM:613662	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003621	PMID:12825077	PCS		2/2			C	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003200	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0000590	PMID:12825077	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001263	OMIM:613662	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0004395	OMIM:613662	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0011923	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0000007	PMID:12825077	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0008347	PMID:12825077	PCS		2/2			P	HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0003737	PMID:12825077	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-20]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0001533	OMIM:613662	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0002027	OMIM:613662	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0002500	OMIM:613662	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613662	Mitochondrial DNA depletion syndrome 4B (mngie type)		HP:0004326	PMID:12825077	PCS		2/2			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-20]
OMIM:102520	Acrorenal syndrome		HP:0012210	OMIM:102520	IEA					P	HPO:iea[2009-02-17]
OMIM:102520	Acrorenal syndrome		HP:0009380	OMIM:102520	TAS					P	HPO:skoehler[2009-02-17]
OMIM:102520	Acrorenal syndrome		HP:0000006	OMIM:102520	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0003444	PMID:24207122	PCS					P	HPO:probinson[2017-05-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0031108	OMIM:615575	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0003431	PMID:24207122	PCS		5/5			P	HPO:probinson[2017-05-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0001288	PMID:24207122	PCS					P	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0001761	OMIM:615575	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0003394	OMIM:615575	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0002380	PMID:24207122	PCS					P	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0009072	PMID:24207122	PCS		10/11			P	HPO:probinson[2017-05-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0007340	OMIM:615575	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0003828	OMIM:615575	TAS					M	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0009046	PMID:24207122	PCS					P	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0007210	OMIM:615575	TAS					P	HPO:probinson[2017-05-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0009005	OMIM:615575	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0007269	PMID:24207122	PCS					P	HPO:probinson[2017-05-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0003701	PMID:24207122	PCS		11/11			P	HPO:probinson[2017-05-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0000006	OMIM:615575	TAS					I	HPO:skoehler[2014-01-28]
OMIM:615575	Neuronopathy, distal hereditary motor, type IID		HP:0003677	OMIM:615575	TAS					C	HPO:skoehler[2014-01-28]
OMIM:263600	Polysaccharide, storage of unusual		HP:0011012	OMIM:263600	TAS					P	HPO:probinson[2015-04-18]
OMIM:263600	Polysaccharide, storage of unusual		HP:0000007	OMIM:263600	TAS					I	HPO:probinson[2009-02-17]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0002069	PMID:29053855	PCS		8/22			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0002384	PMID:29053855	PCS		2/22			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000160	PMID:29053855	PCS		5/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0002121	PMID:29053855	PCS		4/22			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000639	PMID:29053855	PCS		6/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0011463	PMID:29053855	PCS		7/14			C	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0011462	PMID:29053855	PCS		3/14			C	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0005709	PMID:29053855	PCS		1/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0100807	PMID:29053855	PCS		2/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000218	PMID:29053855	PCS		3/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000411	PMID:29053855	PCS		1/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000278	PMID:29053855	PCS		2/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0200021	PMID:29053855	PCS		4/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0001249	PMID:29053855	PCS		16/25			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000472	PMID:29053855	PCS		1/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0003621	PMID:29053855	PCS		4/14			C	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000175	PMID:29053855	PCS		3/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0003189	PMID:29053855	PCS		1/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0002373	PMID:29053855	PCS		1/22			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0001263	PMID:29053855	PCS		2/25			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000470	PMID:29053855	PCS		2/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0045025	PMID:29053855	PCS		1/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0011097	PMID:29053855	PCS		2/22			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0032792	PMID:29053855	PCS		1/22			P	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0001417	PMID:29053855	PCS					I	HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000664	PMID:29053855	PCS		1/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000347	PMID:29053855	PCS		8/15			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:301091	Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features		HP:0000369	PMID:29053855	PCS		3/30			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:610419	Deafness, autosomal recessive 68		HP:0000407	OMIM:610419	TAS					P	HPO:iea[2009-02-17]
OMIM:610419	Deafness, autosomal recessive 68		HP:0003593	OMIM:610419	TAS					C	HPO:iea[2009-02-17]
OMIM:610419	Deafness, autosomal recessive 68		HP:0000007	OMIM:610419	TAS					I	HPO:iea[2009-02-17]
OMIM:615561	Complement factor B deficiency		HP:0002586	PMID:24152280	PCS					P	HPO:skoehler[2015-08-30];HPO:probinson[2020-05-10]
OMIM:615561	Complement factor B deficiency		HP:0001287	PMID:24152280	PCS					P	HPO:probinson[2020-05-10]
OMIM:615561	Complement factor B deficiency		HP:0011463	PMID:24152280	PCS					C	HPO:probinson[2020-05-10]
OMIM:615561	Complement factor B deficiency		HP:0002718	PMID:24152280	PCS					P	HPO:skoehler[2015-08-30];HPO:probinson[2020-05-10]
OMIM:615561	Complement factor B deficiency		HP:0000007	PMID:24152280	PCS					I	HPO:probinson[2020-05-10]
OMIM:615561	Complement factor B deficiency		HP:0005381	PMID:24152280	PCS					P	HPO:skoehler[2015-08-30];HPO:probinson[2020-05-10]
OMIM:615561	Complement factor B deficiency		HP:0002090	PMID:24152280	PCS					P	HPO:skoehler[2015-08-30];HPO:probinson[2020-05-10]
OMIM:615561	Complement factor B deficiency		HP:0005416	PMID:24152280	PCS					P	HPO:skoehler[2015-08-30];HPO:probinson[2020-05-10]
OMIM:267300	Renal tubular acidosis, distal, with progressive nerve deafness		HP:0000407	OMIM:267300	IEA					P	HPO:iea[2009-02-17]
OMIM:267300	Renal tubular acidosis, distal, with progressive nerve deafness		HP:0001947	OMIM:267300	IEA					P	HPO:iea[2009-02-17]
OMIM:267300	Renal tubular acidosis, distal, with progressive nerve deafness		HP:0000007	OMIM:267300	IEA					I	HPO:iea[2009-02-17]
OMIM:267300	Renal tubular acidosis, distal, with progressive nerve deafness		HP:0000787	OMIM:267300	IEA					P	HPO:iea[2009-02-17]
OMIM:615207	Immunodeficiency 56		HP:0004798	PMID:23440042	PCS		4/4			P	HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0001399	PMID:23440042	PCS		1/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0002110	PMID:23440042;PMID:25398835	PCS		2/5			P	HPO:probinson[2021-10-04];HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0001394	PMID:23440042	PCS		1/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0011108	PMID:23440042	PCS		1/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0001508	PMID:23440042	PCS		1/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0002719	PMID:23440042	PCS		4/4			P	HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0011463	PMID:23440042	PCS		4/4			C	HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0000007	PMID:23440042	PCS					I	HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0200124	PMID:23440042	PCS		4/4			P	HPO:skoehler[2013-06-11];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0000403	PMID:25398835	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0030151	PMID:23440042	PCS		4/4			P	HPO:skoehler[2015-01-04];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0006532	PMID:23440042	PCS		4/4			P	HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0020102	PMID:25398835	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0002205	PMID:23440042;PMID:25398835	PCS		5/5			P	HPO:probinson[2021-10-04];HPO:skoehler[2013-05-07];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0002028	PMID:23440042	PCS		2/4			P	HPO:skoehler[2013-05-29];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0002721	PMID:23440042	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2021-10-04]
OMIM:615207	Immunodeficiency 56		HP:0003139	PMID:25398835	PCS		1/1			P	HPO:probinson[2021-10-04]
OMIM:613676	Seckel syndrome 4		HP:0004325	PMID:20522431	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0003510	PMID:20522431	PCS		5/5			P	HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0000252	PMID:20522431	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0003577	PMID:20522431	PCS		2/2			C	HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0000430	PMID:20522431	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0010455	PMID:20522431	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0000007	PMID:20522431	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0000348	PMID:20522431	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0001525	PMID:20522431	PCS		1/2			P	HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0000878	PMID:20522431	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0001511	PMID:20522431	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0000278	PMID:20522431	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:613676	Seckel syndrome 4		HP:0000369	PMID:20522431	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-28]
OMIM:618723	Premature ovarian failure 16		HP:0008209	PMID:30010909	PCS			FEMALE		P	HPO:probinson[2020-05-11]
OMIM:618723	Premature ovarian failure 16		HP:0033085	PMID:30010909	IEA		1/1	FEMALE		P	HPO:probinson[2020-08-13]
OMIM:618723	Premature ovarian failure 16		HP:0008232	PMID:30010909	PCS			FEMALE		P	HPO:probinson[2020-05-11]
OMIM:618723	Premature ovarian failure 16		HP:0008214	PMID:30010909	PCS			FEMALE		P	HPO:probinson[2020-05-11]
OMIM:618723	Premature ovarian failure 16		HP:0000006	PMID:30010909	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:612540	Myopathy, congenital, compton-north		HP:0030799	OMIM:612540	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001252	PMID:19026398	PCS		16/16			P	HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0003593	PMID:19026398	PCS		9/16			C	HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0040081	PMID:19026398	PCS		0/7			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0000316	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001989	OMIM:612540	TAS					P	HPO:skoehler[2013-06-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0000218	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001522	OMIM:612540	IEA					C	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001324	PMID:19026398	PCS		16/16			P	HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0004415	PMID:19026398	PCS		1/16			P	HPO:probinson[2023-02-05];HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001622	PMID:19026398	PCS		4/4			P	HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0003623	PMID:19026398	PCS		7/16			C	HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001166	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001561	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0011968	PMID:19026398	PCS		2/16			P	HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0002033	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001263	PMID:19026398	PCS		2/16			P	HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001284	PMID:19026398	PCS		2/16			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0033333	PMID:19026398	PCS		4/16			P	HPO:probinson[2023-02-05];HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0010557	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0012385	OMIM:612540	TAS					P	HPO:skoehler[2013-10-22]
OMIM:612540	Myopathy, congenital, compton-north		HP:0009473	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001518	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0000007	PMID:19026398	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001558	PMID:19026398	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-05]
OMIM:612540	Myopathy, congenital, compton-north		HP:0002705	OMIM:612540	TAS					P	HPO:skoehler[2015-12-30]
OMIM:612540	Myopathy, congenital, compton-north		HP:0001319	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0002747	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0002304	OMIM:612540	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612540	Myopathy, congenital, compton-north		HP:0000268	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612540	Myopathy, congenital, compton-north		HP:0000300	OMIM:612540	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0001250	OMIM:613886	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0002121	PMID:15494731	PCS		1/1			P	HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0002591	PMID:15494731	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0001252	PMID:15494731	PCS	HP:0003593	1/1			P	HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0003593	PMID:15494731	PCS		1/1			C	HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0012448	OMIM:613886	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0011344	PMID:15494731	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0000729	OMIM:613886	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0000817	OMIM:613886	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0000733	PMID:15494731	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0001513	PMID:15494731	PCS		1/1			P	HPO:probinson[2013-08-10];HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0000006	PMID:15494731	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2023-01-23]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0001249	OMIM:613886	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613886	Obesity, hyperphagia, and developmental delay		HP:0000324	OMIM:613886	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0003774	PMID:21756023	PCS		1/5			P	HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0003676	PMID:21756023	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0003621	PMID:21756023	PCS		1/4			C	HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0000100	PMID:21756023	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0000969	PMID:21756023	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0011463	PMID:21756023	PCS		3/4			C	HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0000097	PMID:21756023	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0000790	PMID:21756023	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0003073	PMID:21756023	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0000007	PMID:21756023	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0000093	PMID:21756023	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:614131	Focal segmental glomerulosclerosis 6		HP:0000092	PMID:21756023	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-18]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0003477	OMIM:610357	TAS		HP:0040282			P	HPO:skoehler[2012-11-21]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0003487	OMIM:610357	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0001310	OMIM:610357	TAS		HP:0040282			P	HPO:skoehler[2012-11-21]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0001272	OMIM:610357	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0001251	OMIM:610357	TAS		HP:0040282			P	HPO:skoehler[2012-11-21]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0002064	OMIM:610357	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0002061	OMIM:610357	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0011448	OMIM:610357	TAS					P	HPO:probinson[2012-04-26]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0007340	OMIM:610357	TAS		HP:0040282			P	HPO:skoehler[2012-11-21]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0007210	OMIM:610357	TAS		HP:0040282			P	HPO:skoehler[2012-11-21]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0002839	OMIM:610357	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0000007	OMIM:610357	IEA					I	HPO:skoehler[2010-06-19]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0001258	OMIM:610357	TAS					P	HPO:skoehler[2015-01-21]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0003677	OMIM:610357	IEA					C	HPO:skoehler[2010-06-19]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0000006	PMID:25585697	IEA					I	HPO:probinson[2020-07-17]
OMIM:610357	Spastic paraplegia 30, autosomal recessive		HP:0001347	OMIM:610357	IEA					P	HPO:skoehler[2010-06-19]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0031834	PMID:24254849	PCS		1/6			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0001660	PMID:24254849;PMID:35396997	PCS		5/10			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0003577	PMID:24254849	PCS		1/6			C	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0005268	PMID:35396997	PCS		3/4			C	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0030674	PMID:24254849	PCS		3/6			C	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0003593	PMID:24254849	PCS		2/6			C	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0004383	PMID:35396997	PCS		3/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0031632	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0033568	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0011579	PMID:24254849	PCS		1/6			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0011680	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0034199	PMID:35396997	PCS		1/3			C	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0034198	PMID:35396997	PCS		2/3			C	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0001719	PMID:24254849	PCS		1/6			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0011560	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0001669	PMID:24254849	PCS		1/6			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0000767	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0000007	PMID:24254849	PCS					I	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0004935	PMID:24254849	PCS		1/6			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0001511	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0001642	PMID:24254849	PCS		1/6			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0000476	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:620294	Congenital heart defects, multiple types, 9		HP:0000369	PMID:35396997	PCS		1/4			P	HPO:probinson[2023-07-06]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0002257	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0012265	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0002783	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0002110	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0002837	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0000403	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0012735	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0000007	OMIM:616726	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0006532	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0000405	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616726	Ciliary dyskinesia, primary, 33		HP:0100750	PMID:26387594	PCS					P	HPO:probinson[2017-06-17]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0001265	PMID:25192047	PCS					P	HPO:skoehler[2014-10-10];HPO:probinson[2022-03-12]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0000365	PMID:25192047	PCS		2/10			P	HPO:skoehler[2014-10-10];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0001761	PMID:25192047	PCS		7/10			P	HPO:skoehler[2014-10-10];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0003388	PMID:25192047	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0025680	PMID:25192047	PCS		6/8			P	HPO:probinson[2022-02-03]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0003693	PMID:25192047	PCS		4/10			P	HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0001284	PMID:25192047	PCS		10/10			P	HPO:skoehler[2014-10-10];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0002460	PMID:25192047	PCS		5/10			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0001270	PMID:25192047	PCS		1/10			P	HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0033383	PMID:25192047	PCS		8/9			P	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0011463	PMID:25192047	PCS					C	HPO:probinson[2022-03-12]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0009027	PMID:25192047	PCS		6/10			P	HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0002936	PMID:25192047	PCS		2/10			P	HPO:probinson[2021-10-16];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0002515	PMID:25192047	PCS		4/10			P	HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0007126	PMID:25192047	PCS		1/10			P	HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0003701	PMID:25192047	PCS		3/10			P	HPO:skoehler[2014-10-10];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0001763	PMID:25192047	PCS		1/10			P	HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0000006	PMID:25192047	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-10-16]
OMIM:616040	Myasthenic syndrome, congenital, 7, presynaptic		HP:0001765	PMID:25192047	PCS		8/10			P	HPO:skoehler[2014-10-10];HPO:probinson[2021-10-16]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0000286	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0000750	PMID:33711248	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0002188	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0004322	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0031936	PMID:33711248	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0003593	PMID:33711248	PCS		2/2			C	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0032794	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0011097	PMID:33711248	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0000316	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0000218	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0000565	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0007359	PMID:33711248	PCS		1/2			P	HPO:probinson[2021-08-20]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0000006	PMID:33711248	PCS					I	HPO:probinson[2021-08-16];HPO:probinson[2021-08-16]
OMIM:619373	Neurodevelopmental disorder with infantile epileptic spasms		HP:0001249	PMID:33711248	PCS		2/2			P	HPO:probinson[2021-08-20]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0003236	PMID:22522420	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000541	PMID:22522420	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0002365	PMID:22522420	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001252	OMIM:614643	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001290	OMIM:614643	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0031882	OMIM:614643	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0002084	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0002282	OMIM:614643	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0007260	PMID:22522420	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000518	PMID:22522420	PCS		4/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0008551	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001305	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000238	PMID:22522420	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000659	PMID:22522420	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0002119	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001302	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001522	PMID:22522420	PCS		3/5			C	HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000256	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000278	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0007968	PMID:22522420	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001321	PMID:22522420	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0002079	PMID:22522420	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000490	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001284	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0003560	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001181	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000609	PMID:22522420	PCS		2/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0032391	PMID:22522420	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0003819	PMID:22522420	PCS		2/5			C	HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001339	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000007	PMID:22522420	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001558	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000568	PMID:22522420	PCS		3/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0001338	PMID:22522420	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0007973	OMIM:614643	TAS					P	HPO:skoehler[2013-02-25]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0002007	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000501	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0000369	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7		HP:0002126	OMIM:614643	TAS					P	HPO:skoehler[2012-10-17]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000483	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0007957	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0003236	OMIM:175780	TAS					P	HPO:skoehler[2014-07-11]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002301	PMID:15905400	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001332	PMID:15905400	PCS		1/10			P	HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001250	PMID:15905400	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002140	OMIM:175780	IEA					P	HPO:skoehler[2010-06-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000482	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0003593	PMID:15905400	PCS		1/9			C	HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0500087	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0011463	PMID:15905400	PCS		4/9			C	HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000519	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0003829	OMIM:175780	IEA					I	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002539	OMIM:175780	IEA					P	HPO:skoehler[2018-10-08]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000238	OMIM:175780	IEA					P	HPO:skoehler[2010-06-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001249	PMID:15905400	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001342	OMIM:175780;PMID:15905400	PCS		12/16			P	HPO:probinson[2022-08-04];HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0003487	PMID:15905400	PCS		1/10			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000573	PMID:15905400	PCS		1/6			P	HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002076	OMIM:175780	IEA					P	HPO:skoehler[2019-09-07]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002352	PMID:15905400	PCS		6/6			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002077	PMID:15905400	PCS		3/6			P	HPO:probinson[2022-08-04];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002273	OMIM:175780	IEA					P	HPO:iea[2009-02-17]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0032046	OMIM:175780	IEA					P	HPO:skoehler[2019-02-22]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0010636	OMIM:175780	TAS					P	HPO:skoehler[2014-07-11]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0011496	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000646	OMIM:175780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000568	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0007676	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001136	PMID:15905400	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001257	OMIM:175780	IEA					P	HPO:skoehler[2010-06-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0007359	PMID:15905400	PCS		1/10			P	HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000006	PMID:15905400	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0003577	PMID:15905400	PCS		4/9			C	HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000540	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001272	OMIM:175780	TAS					P	HPO:skoehler[2014-07-11]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0009918	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0007663	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001269	PMID:15905400	PCS		6/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000577	OMIM:175780	IEA					P	HPO:iea[2009-02-17]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0007209	OMIM:175780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001123	OMIM:175780	IEA					P	HPO:iea[2009-02-17]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002451	OMIM:175780	IEA					P	HPO:iea[2009-02-17]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0002132	PMID:15905400	PCS		8/10			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0011500	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0012520	PMID:15905400	PCS		6/6			P	HPO:probinson[2022-08-04]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0001878	OMIM:175780	TAS					P	HPO:skoehler[2014-07-11]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0007894	OMIM:175780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000622	OMIM:175780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000501	OMIM:175780	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:175780	Brain small vessel disease 1 with or without ocular anomalies		HP:0000545	OMIM:175780	IEA					P	HPO:skoehler[2019-04-18]
OMIM:619367	Angioedema, hereditary, 8		HP:0002014	PMID:33508266	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0100665	PMID:33508266	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0000282	PMID:33508266	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0002572	PMID:33508266	PCS					P	HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0031244	PMID:33508266	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0012027	PMID:33508266	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0000006	PMID:33508266	PCS					I	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0007514	PMID:33508266	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619367	Angioedema, hereditary, 8		HP:0002027	PMID:33508266	PCS				HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0010628	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003676	OMIM:254090	IEA					C	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0002783	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001371	OMIM:254090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0020152	PMID:16258657	PCS					P	HPO:probinson[2019-09-07]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003593	OMIM:254090	IEA					C	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001270	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0005072	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001508	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003828	OMIM:254090	IEA					M	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0008872	OMIM:254090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0000975	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0000218	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003803	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0000411	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003701	OMIM:254090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0007502	OMIM:254090	IEA					P	HPO:skoehler[2010-06-18]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0002877	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0000311	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003306	PMID:12011280	PCS		15/15			P	HPO:iea[2009-02-17];HP:probinson[2019-06-04]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001249	PMID:12011280	PCS		0/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-03-09]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003700	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0000473	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0002650	PMID:12011280	PCS		12/15			P	HPO:iea[2009-02-17];HP:probinson[2019-06-04]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001762	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001382	PMID:12011280	PCS		12/12			P	HPO:skoehler[2010-06-20];HP:probinson[2019-06-04]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003560	OMIM:254090	IEA					P	HPO:skoehler[2015-01-19]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0002093	OMIM:254090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0008180	OMIM:254090	IEA					P	HPO:skoehler[2010-06-20]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0006460	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0002808	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0002827	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0000007	OMIM:254090	IEA					I	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001319	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0002747	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0030095	PMID:12011280	PCS		6/11			P	HP:probinson[2019-06-04]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0001533	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0006149	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003713	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0000006	OMIM:254090	IEA					I	HPO:skoehler[2010-06-19]
OMIM:254090	Ullrich congenital muscular dystrophy 1		HP:0003557	OMIM:254090	IEA					P	HPO:iea[2009-02-17]
OMIM:610425	Cataract 23		HP:0100018	PMID:20577656	PCS	HP:0003577	2/2			P	HPO:probinson[2024-02-15]
OMIM:610425	Cataract 23		HP:0000482	PMID:20577656	PCS		2/2			P	HPO:probinson[2024-02-15]
OMIM:610425	Cataract 23		HP:0007971	PMID:16960806	PCS	HP:0011463				P	HPO:probinson[2013-02-28]
OMIM:610425	Cataract 23		HP:0000006	PMID:16960806	PCS					I	HPO:probinson[2013-01-09]
OMIM:620280	Deafness, autosomal dominant 86		HP:0001751	PMID:32776944	PCS		0/15			P	HPO:probinson[2023-06-18]
OMIM:620280	Deafness, autosomal dominant 86		HP:0000407	PMID:32776944	PCS	HP:0003581	15/15			P	HPO:probinson[2023-06-18]
OMIM:620280	Deafness, autosomal dominant 86		HP:0003581	PMID:32776944	PCS		15/15			C	HPO:probinson[2023-06-18]
OMIM:620280	Deafness, autosomal dominant 86		HP:0000360	PMID:32776944	PCS		15/15			P	HPO:probinson[2023-06-18]
OMIM:620280	Deafness, autosomal dominant 86		HP:0011390	PMID:32776944	PCS		0/1			P	HPO:probinson[2023-06-18]
OMIM:620280	Deafness, autosomal dominant 86		HP:0000006	PMID:32776944	PCS					I	HPO:probinson[2023-06-18]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0030644	PMID:26593267	PCS		1/5			P	HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0000551	PMID:26593267	PCS		4/4			P	HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0001251	PMID:26593267	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0032794	PMID:26593267	PCS		1/6			P	HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0000639	PMID:26593267	PCS	HP:0003593	2/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0011463	PMID:26593267	PCS					C	HPO:probinson[2021-03-13];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0000613	PMID:26593267	PCS		5/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0007663	PMID:26593267	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0000007	PMID:26593267	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0000603	PMID:26593267	PCS		2/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0000543	PMID:26593267	PCS		6/6			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-03-13]
OMIM:616732	Optic atrophy 10 with or without ataxia, impaired intellectual development and seizures		HP:0007976	PMID:26593267	PCS		1/6			P	HPO:probinson[2021-03-13]
OMIM:619401	Lymphatic malformation 11		HP:0003621	PMID:32947856	PCS		2/3			C	HPO:probinson[2021-07-10]
OMIM:619401	Lymphatic malformation 11		HP:0011462	PMID:32947856	PCS		1/3			C	HPO:probinson[2021-07-10]
OMIM:619401	Lymphatic malformation 11		HP:0010741	PMID:32947856	PCS		4/4			P	HPO:probinson[2021-07-10]
OMIM:619401	Lymphatic malformation 11		HP:0001004	PMID:32947856	PCS		2/4			P	HPO:probinson[2021-07-10]
OMIM:619401	Lymphatic malformation 11		HP:0000006	PMID:32947856	PCS					I	HPO:probinson[2021-07-10];HPO:probinson[2021-07-10]
OMIM:609612	Fibrosis of extraocular muscles, congenital, with synergistic divergence		HP:0000508	OMIM:609612	TAS					P	HPO:skoehler[2014-02-06]
OMIM:609612	Fibrosis of extraocular muscles, congenital, with synergistic divergence		HP:0000006	OMIM:609612	TAS					I	HPO:skoehler[2014-02-06]
OMIM:609612	Fibrosis of extraocular muscles, congenital, with synergistic divergence		HP:0000577	OMIM:609612	TAS					P	HPO:skoehler[2014-02-06]
OMIM:164100	Nystagmus 2, congenital, autosomal dominant		HP:0000486	OMIM:164100	PCS					P	HPO:probinson[2012-04-01]
OMIM:164100	Nystagmus 2, congenital, autosomal dominant		HP:0003593	OMIM:164100	TAS					C	HPO:skoehler[2012-10-17]
OMIM:164100	Nystagmus 2, congenital, autosomal dominant		HP:0007663	OMIM:164100	TAS					P	HPO:skoehler[2015-07-20]
OMIM:164100	Nystagmus 2, congenital, autosomal dominant		HP:0000505	OMIM:164100	PCS				HP:0012825	P	HPO:probinson[2012-04-01]
OMIM:164100	Nystagmus 2, congenital, autosomal dominant		HP:0032037	OMIM:164100	IEA					P	HPO:skoehler[2019-02-22]
OMIM:164100	Nystagmus 2, congenital, autosomal dominant		HP:0000006	OMIM:164100	IEA					I	HPO:iea[2009-02-17]
OMIM:164100	Nystagmus 2, congenital, autosomal dominant		HP:0000666	OMIM:164100	PCS				HP:0012825	P	HPO:probinson[2012-04-01]
OMIM:129000	Earring holes, natural		HP:0004461	OMIM:129000	TAS					P	HPO:iea[2009-02-17]
OMIM:129000	Earring holes, natural		HP:0000006	OMIM:129000	TAS					I	HPO:iea[2009-02-17]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000286	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0030799	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0003577	PMID:26220823	PCS		8/8			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0004322	PMID:26220823	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000243	PMID:26220823	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001970	PMID:26220823	PCS		1/8			P	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0004442	PMID:26220823	PCS		1/8			P	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0045075	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001629	PMID:26220823	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0011220	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000316	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001305	PMID:26220823	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001800	PMID:26220823	PCS		3/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000653	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001522	PMID:26220823	PCS		1/8			C	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001763	PMID:26220823	PCS		1/8			P	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001249	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001320	PMID:26220823	PCS		4/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000494	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000695	PMID:26220823	PCS		1/8			P	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0001263	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000790	PMID:26220823	PCS		1/8			P	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000093	PMID:26220823	PCS		1/8			P	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0005280	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0003819	PMID:26220823	PCS		2/8			C	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0002209	PMID:26220823	PCS		8/8			P	HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000007	PMID:26220823	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000369	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		HP:0000347	PMID:26220823	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-09]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0001892	PMID:20966167	PCS					P	HPO:skoehler[2009-02-17]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0031364	OMIM:609821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0000007	PMID:20966167	PCS					I	HPO:probinson[2009-02-17]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0000978	PMID:1333302	PCS					P	HPO:probinson[2009-02-17]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0001934	PMID:20966167	PCS					P	HPO:probinson[2013-12-14]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0004846	PMID:20966167	PCS					P	HPO:probinson[2013-12-14]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0000421	PMID:10816552	PCS					P	HPO:probinson[2009-02-17]
OMIM:609821	Bleeding disorder, platelet-type, 8		HP:0004866	PMID:20966167	PCS					P	HPO:probinson[2009-02-17]
OMIM:136120	Fish-Eye disease		HP:0007759	OMIM:136120	TAS					P	HPO:skoehler[2009-02-17]
OMIM:136120	Fish-Eye disease		HP:0002155	OMIM:136120	TAS					P	HPO:skoehler[2009-02-17]
OMIM:136120	Fish-Eye disease		HP:0003233	OMIM:136120	TAS					P	HPO:skoehler[2013-02-25]
OMIM:136120	Fish-Eye disease		HP:0003141	OMIM:136120	TAS					P	HPO:probinson[2013-12-15]
OMIM:136120	Fish-Eye disease		HP:0003362	OMIM:136120	TAS					P	HPO:probinson[2009-02-17]
OMIM:136120	Fish-Eye disease		HP:0000007	OMIM:136120	TAS					I	HPO:skoehler[2012-10-17]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000286	PMID:29985992	PCS		1/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000343	PMID:29985992	PCS		9/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000540	PMID:29985992	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000160	PMID:29985992	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0001252	PMID:29985992	PCS		4/12			P	HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0003593	PMID:29985992	PCS		12/12			C	HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0012745	PMID:29985992	PCS		7/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0001270	PMID:29985992	PCS		11/12			P	HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0031545	PMID:29985992	PCS		1/12			P	HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0045074	PMID:29985992	PCS		5/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0002719	PMID:29985992	PCS		4/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000739	PMID:29985992	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000316	PMID:29985992	PCS		7/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000219	PMID:29985992	PCS		11/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0002317	PMID:29985992	PCS		1/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0001249	PMID:29985992	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000677	PMID:29985992	PCS		5/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0002058	PMID:29985992	PCS		6/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0001880	PMID:29985992	PCS		4/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000750	PMID:29985992	PCS		12/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0031936	PMID:29985992	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0011968	PMID:29985992	PCS		3/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0002099	PMID:29985992	PCS		7/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0001263	PMID:29985992	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000691	PMID:29985992	PCS		5/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000729	PMID:29985992	PCS		4/12			P	HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000668	PMID:29985992	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000448	PMID:29985992	PCS		9/12			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0001257	PMID:29985992	PCS		1/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000006	PMID:29985992	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-23]
OMIM:618092	Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities		HP:0000545	PMID:29985992	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-23]
OMIM:117850	Cervical hypertrichosis with underlying kyphoscoliosis		HP:0002751	OMIM:117850	TAS					P	HPO:probinson[2009-02-17]
OMIM:117850	Cervical hypertrichosis with underlying kyphoscoliosis		HP:0004532	OMIM:117850	TAS					P	HPO:probinson[2009-02-17]
OMIM:117850	Cervical hypertrichosis with underlying kyphoscoliosis		HP:0011913	OMIM:117850	TAS					P	HPO:probinson[2012-07-18]
OMIM:117850	Cervical hypertrichosis with underlying kyphoscoliosis		HP:0011914	OMIM:117850	TAS					P	HPO:probinson[2012-07-18]
OMIM:117850	Cervical hypertrichosis with underlying kyphoscoliosis		HP:0000006	OMIM:117850	TAS					I	HPO:probinson[2009-02-17]
OMIM:117850	Cervical hypertrichosis with underlying kyphoscoliosis		HP:0004535	OMIM:117850	TAS					P	HPO:probinson[2009-02-17]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0008935	OMIM:614870	TAS					P	HPO:probinson[2013-02-24]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0003577	PMID:17041890	PCS		1/1			C	HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0001410	OMIM:614870	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0000431	PMID:17041890	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0030048	OMIM:614870	IEA					P	HPO:skoehler[2019-02-22]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0001250	PMID:17041890	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0001252	PMID:17041890	PCS		1/1			P	HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0002240	OMIM:614870	TAS					P	HPO:probinson[2013-02-24]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0011344	OMIM:614870	TAS					P	HPO:probinson[2013-02-24]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0010655	OMIM:614870	TAS					P	HPO:probinson[2013-02-24]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0000107	PMID:17041890	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0000007	PMID:9683594	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0008872	OMIM:614870	TAS					P	HPO:probinson[2013-02-24]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0001302	OMIM:614870	TAS					P	HPO:probinson[2013-02-24]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0003811	PMID:17041890	PCS		1/1			C	HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0000369	PMID:17041890	PCS		1/1			P	HPO:skoehler[2019-02-22];HPO:probinson[2023-02-09]
OMIM:614870	Peroxisome biogenesis disorder 6A (Zellweger)		HP:0003678	OMIM:614870	IEA					C	HPO:skoehler[2019-02-22]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0000452	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0004440	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0000272	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0000327	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0000007	OMIM:241310	IEA					I	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0000205	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0001643	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0012730	OMIM:241310	TAS					P	HPO:skoehler[2014-03-24]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0001631	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0000347	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:241310	Hypomandibular faciocranial dysostosis		HP:0000588	OMIM:241310	IEA					P	HPO:iea[2009-02-17]
OMIM:618086	Spermatogenic failure 28		HP:0011969	PMID:30075111	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-29]
OMIM:618086	Spermatogenic failure 28		HP:0003251	PMID:30075111	PCS		3/3			P	HPO:probinson[2023-03-29]
OMIM:618086	Spermatogenic failure 28		HP:0011462	PMID:30075111	PCS		3/3			C	HPO:probinson[2023-03-29]
OMIM:618086	Spermatogenic failure 28		HP:0008232	PMID:30075111	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-29]
OMIM:618086	Spermatogenic failure 28		HP:0000007	PMID:30075111	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-29]
OMIM:618086	Spermatogenic failure 28		HP:0040171	PMID:30075111	PCS		1/3			P	HPO:probinson[2023-03-29]
OMIM:618086	Spermatogenic failure 28		HP:0008734	PMID:30075111	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-29]
OMIM:618086	Spermatogenic failure 28		HP:0011961	PMID:30075111	PCS		3/3			P	HPO:probinson[2023-03-29]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0007957	PMID:35933355;PMID:35924320;PMID:28069640	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0025169	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		12/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0003593	PMID:32666529;PMID:35933355;PMID:28069640	PCS		6/13			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0410030	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0030718	PMID:35924320;PMID:28069640	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001270	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		5/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0011359	PMID:35933355;PMID:28069640	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001629	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001508	PMID:35933355;PMID:35924320;PMID:28069640	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0011463	PMID:32666529;PMID:35924320;PMID:28069640	PCS		7/13			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001806	PMID:32666529;PMID:35933355;PMID:28069640	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001647	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0004756	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001249	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001644	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001561	PMID:32666529;PMID:35933355	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0031318	PMID:35924320;PMID:28069640	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0003621	PMID:32666529	PCS		1/7			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001685	PMID:35924320;PMID:28069640	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0034306	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		3/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0005280	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0005180	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		4/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0012413	PMID:35924320	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0040149	PMID:32666529;PMID:35933355;PMID:28069640	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0009890	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0008064	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0002209	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0000007	PMID:28069640	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0000989	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0002208	PMID:35933355;PMID:35924320	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001698	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0008404	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001653	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		4/13			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0000982	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		0/12			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620519	Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities		HP:0001655	PMID:32666529;PMID:35933355;PMID:35924320;PMID:28069640	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003202	PMID:10507732	PCS		20/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003236	PMID:10507732	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003621	PMID:10507732	PCS		3/20			C	HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003555	PMID:10507732	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0002650	PMID:10507732	PCS		1/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0001371	PMID:10507732	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0005133	PMID:10507732	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003560	PMID:10507732	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003391	OMIM:253700	IEA					P	HPO:iea[2009-02-17]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0002090	PMID:10507732	PCS		5/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0002091	PMID:10507732	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0100297	PMID:10507732	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0011463	PMID:10507732	PCS		17/20			C	HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003707	PMID:10507732	PCS		2/20			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0000007	PMID:10507732	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003307	OMIM:253700	IEA					P	HPO:iea[2009-02-17]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0002505	PMID:10507732	PCS		20/20			P	HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003803	PMID:10507732	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003713	OMIM:253700	IEA					P	HPO:iea[2009-02-17]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0001667	PMID:10507732	PCS		0/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003678	PMID:10507732	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:253700	Muscular dystrophy, limb-girdle, type 2C		HP:0003557	PMID:10507732	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0003565	PMID:33674380	PCS		1/1			P	HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0100279	PMID:33674380	PCS		1/1			P	HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0001903	PMID:33674380	PCS		1/1			P	HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0003593	PMID:33674380	PCS		1/1			C	HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0000007	PMID:33674380	PCS					I	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0001270	PMID:33674380	PCS		1/1			P	HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0025085	PMID:33674380	PCS		1/1			P	HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0011227	PMID:33674380	PCS		1/1			P	HPO:probinson[2021-07-14]
OMIM:619398	Inflammatory bowel disease (infantile ulcerative colitis) 31		HP:0001974	PMID:33674380	PCS		1/1			P	HPO:probinson[2021-07-14]
OMIM:257200	Niemann-Pick disease, type A		HP:0002540	PMID:16434659	PCS		10/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0002188	PMID:16434659	PCS		3/3			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0004322	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0001252	PMID:16434659	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0002063	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0010729	PMID:16434659	PCS		10/10			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0002240	PMID:16434659	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0003593	PMID:16434659	PCS		10/10			C	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0031964	PMID:16434659	PCS		10/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0000939	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0001508	PMID:16434659	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0000737	PMID:16434659	PCS		10/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0003609	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0008872	PMID:16434659	PCS	HP:0003593	10/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0002716	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0001324	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0002019	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0000256	PMID:16434659	PCS		2/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0001249	OMIM:257200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:257200	Niemann-Pick disease, type A		HP:0006579	PMID:16434659	PCS		1/10			P	HPO:probinson[2012-07-19];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0001744	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0001265	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0003202	PMID:16434659	PCS		10/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0031956	PMID:16434659	PCS		10/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0001982	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0004333	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0002013	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0000991	OMIM:257200	TAS					P	HPO:probinson[2012-07-19]
OMIM:257200	Niemann-Pick disease, type A		HP:0002376	PMID:16434659	PCS		10/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0001541	PMID:16434659	PCS		2/10			P	HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0001263	PMID:16434659	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0000007	OMIM:257200	IEA					I	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0002207	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0001935	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0001538	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0002205	PMID:16434659	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-03-13]
OMIM:257200	Niemann-Pick disease, type A		HP:0002305	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:257200	Niemann-Pick disease, type A		HP:0001257	OMIM:257200	IEA					P	HPO:iea[2009-02-17]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0001562	PMID:32427860	IEA	HP:0030674	2/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0011471	PMID:32427860	PCS	HP:0003593	1/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0000252	PMID:32427860	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0001344	PMID:32427860	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0001332	PMID:32427860	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0001518	PMID:32427860	PCS	HP:0003577	1/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0032794	PMID:32427860	PCS	HP:0003593	2/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0001290	PMID:32427860	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0000007	PMID:32427860	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0011344	PMID:32427860	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0003429	PMID:32427860	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618910	Epileptic encephalopathy, early infantile, 86		HP:0003700	PMID:32427860	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:252350	Moyamoya disease 1		HP:0012474	OMIM:252350	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252350	Moyamoya disease 1		HP:0001009	OMIM:252350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:252350	Moyamoya disease 1		HP:0000007	OMIM:252350	IEA					I	HPO:iea[2009-02-17]
OMIM:252350	Moyamoya disease 1		HP:0005291	OMIM:252350	IEA					P	HPO:iea[2009-02-17]
OMIM:156830	Micromelic bone dysplasia with cloverleaf skull		HP:0002983	OMIM:156830	TAS					P	HPO:skoehler[2009-02-17]
OMIM:156830	Micromelic bone dysplasia with cloverleaf skull		HP:0000007	PMID:4073120	TAS					I	HPO:nvasilevsky[2019-03-12];HPO:nvasilevsky[2019-03-12]
OMIM:156830	Micromelic bone dysplasia with cloverleaf skull		HP:0002676	OMIM:156830	TAS					P	HPO:skoehler[2009-02-17]
OMIM:156830	Micromelic bone dysplasia with cloverleaf skull		HP:0000006	OMIM:156830	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0003554	PMID:21255763	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001252	PMID:21255763	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0003593	PMID:21255763	PCS		3/3			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0012622	PMID:21255763	PCS					P	HPO:skoehler[2014-01-18];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0000819	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001508	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0002917	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001903	PMID:21255763	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0004719	PMID:21255763	PCS		2/2			P	HPO:skoehler[2013-04-18];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0002878	PMID:21255763	PCS		2/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001622	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001882	PMID:21255763	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0011968	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0002151	PMID:21255763	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001263	PMID:21255763	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0000093	PMID:21255763	PCS		1/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0002092	PMID:21255763	PCS		3/3			P	HPO:skoehler[2013-05-29];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0002093	PMID:21255763	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0002902	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0000007	PMID:21255763	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0000103	PMID:21255763	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001873	PMID:21255763	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0005977	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0000127	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0003138	PMID:21255763	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0001876	PMID:21255763	PCS		1/3			P	HPO:probinson[2023-02-04]
OMIM:613845	Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome		HP:0002149	PMID:21255763	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-04]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000154	PMID:25217958	PCS		2/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000396	PMID:25217958	PCS		1/7			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0002069	PMID:25217958	PCS		1/7			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000582	PMID:25217958	PCS		1/7			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000750	PMID:25217958	PCS		6/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0001263	PMID:25217958	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0001252	PMID:25217958	PCS		5/6			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0003593	PMID:25217958	PCS					C	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0001270	PMID:25217958	PCS		5/5			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0012760	PMID:25217958	PCS		5/7			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000718	PMID:25217958	PCS		3/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000508	PMID:25217958	PCS		2/7			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000316	PMID:25217958	PCS		1/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000664	PMID:25217958	PCS		1/7			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0002558	PMID:25217958	PCS		1/7			P	HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000006	PMID:25217958	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-14]
OMIM:616083	Intellectual developmental disorder, autosomal dominant 30		HP:0000248	PMID:25217958	PCS		1/7			P	HPO:probinson[2022-06-14]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0002344	PMID:27435091	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0002069	PMID:27435091	PCS		4/7			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0003236	PMID:27435091	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0002521	PMID:27435091	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0002510	PMID:27435091	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0001332	PMID:27435091	PCS		2/6			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0011968	PMID:27435091	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0001250	PMID:27435091	PCS		7/7		HP:0031375	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0002151	OMIM:617389	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0001263	PMID:27435091	PCS		2/2			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0001252	PMID:27435091	PCS		6/7			P	HPO:probinson[2023-02-23];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0003593	PMID:27435091	PCS		2/7			C	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0032794	PMID:27435091	PCS		6/7			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0033725	PMID:27435091	PCS		1/7			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0011097	PMID:27435091	PCS		2/7			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0032792	PMID:27435091	PCS		4/7			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0032660	PMID:27435091	PCS		1/7			P	HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0000007	PMID:27435091	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0200134	PMID:27435091	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0000505	PMID:27435091	PCS		3/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-23]
OMIM:617389	Epileptic encephalopathy, early infantile, 53		HP:0003623	PMID:27435091	PCS		5/7			C	HPO:probinson[2023-02-23]
OMIM:145680	Dystransthyretinemic euthyroidal hyperthyroxinemia		HP:0008247	OMIM:145680	IEA					P	HPO:probinson[2012-03-25]
OMIM:145680	Dystransthyretinemic euthyroidal hyperthyroxinemia		HP:0000006	OMIM:145680	IEA					I	HPO:probinson[2012-03-25]
OMIM:165550	Optic nerve hypoplasia		HP:0000609	PMID:12721955	PCS		4/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:165550	Optic nerve hypoplasia		HP:0007968	PMID:12721955	PCS		2/8			P	HPO:probinson[2021-02-25]
OMIM:165550	Optic nerve hypoplasia		HP:0000639	PMID:12721955	PCS		4/8			P	HPO:probinson[2021-02-25]
OMIM:165550	Optic nerve hypoplasia		HP:0007663	PMID:12721955	PCS		8/8			P	HPO:skoehler[2015-07-26];HPO:probinson[2021-02-25]
OMIM:165550	Optic nerve hypoplasia		HP:0025514	PMID:12721955	PCS		1/8			P	HPO:probinson[2021-02-25]
OMIM:165550	Optic nerve hypoplasia		HP:0000505	PMID:12721955	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:165550	Optic nerve hypoplasia		HP:0012521	PMID:12721955	PCS		2/8			P	HPO:skoehler[2015-01-21];HPO:probinson[2021-02-25]
OMIM:165550	Optic nerve hypoplasia		HP:0000006	PMID:12721955	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-25]
OMIM:614858	Hypogonadotropic hypogonadism 14 with or without anosmia		HP:0000044	PMID:20887964	PCS		6/7			P	HPO:probinson[2022-11-26]
OMIM:614858	Hypogonadotropic hypogonadism 14 with or without anosmia		HP:0000458	PMID:20887964	PCS		2/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-26]
OMIM:614858	Hypogonadotropic hypogonadism 14 with or without anosmia		HP:0008734	PMID:20887964	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-26]
OMIM:614858	Hypogonadotropic hypogonadism 14 with or without anosmia		HP:0000006	PMID:20887964	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-26]
OMIM:614858	Hypogonadotropic hypogonadism 14 with or without anosmia		HP:0000028	PMID:20887964	PCS		1/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-11-26]
OMIM:614858	Hypogonadotropic hypogonadism 14 with or without anosmia		HP:0000786	PMID:20887964	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-11-26]
OMIM:613689	Mammary-Digital-Nail syndrome		HP:0002164	OMIM:613689	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613689	Mammary-Digital-Nail syndrome		HP:0010313	OMIM:613689	TAS			FEMALE		P	HPO:skoehler[2013-06-03]
OMIM:613689	Mammary-Digital-Nail syndrome		HP:0008404	OMIM:613689	TAS					P	HPO:skoehler[2013-05-03]
OMIM:613689	Mammary-Digital-Nail syndrome		HP:0000006	OMIM:613689	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613689	Mammary-Digital-Nail syndrome		HP:0001798	OMIM:613689	TAS					P	HPO:skoehler[2012-10-17]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0003577	PMID:30642273	PCS		3/3			C	HPO:probinson[2023-01-20]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0012542	PMID:30642273	PCS		3/3			P	HPO:probinson[2023-01-20]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0002164	PMID:30642273	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-20]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0001805	OMIM:161050	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0001806	PMID:30642273	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-20]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0000007	PMID:23374899	PCS					I	HPO:probinson[2020-07-17]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0030804	OMIM:161050	IEA					P	HPO:skoehler[2018-10-08]
OMIM:161050	Nail disorder, nonsyndromic congenital, 1		HP:0003677	OMIM:161050	TAS					C	HPO:skoehler[2012-10-17]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0000252	PMID:35953447	PCS		1/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0000750	PMID:35455965;PMID:35953447	PCS		3/6		HP:0012825	P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0002188	PMID:35455965;PMID:35953447	PCS		6/6			P	HPO:probinson[2023-06-15];HPO:probinson[2023-06-15];HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0031936	PMID:35455965	PCS		2/2			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0001332	PMID:35953447	PCS		1/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0001250	PMID:35953447	PCS		3/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0002066	PMID:35953447	PCS		2/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0001260	PMID:35953447	PCS		1/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0001252	PMID:35455965;PMID:35953447	PCS		5/6			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0000592	PMID:35953447	PCS		1/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0001263	PMID:35953447	PCS		3/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0003593	PMID:35455965	PCS		1/2			C	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0031987	PMID:35953447	PCS		1/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0000639	PMID:35455965;PMID:35953447	PCS		6/6			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0011342	PMID:35455965	PCS		2/2			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0000817	PMID:35953447	PCS		1/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0001510	PMID:35953447	PCS		1/4			P	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0000006	PMID:35455965	PCS					I	HPO:probinson[2023-06-15]
OMIM:620243	Leukodystrophy, hypomyelinating, 25		HP:0003623	PMID:35455965;PMID:35953447	PCS		5/6			C	HPO:probinson[2023-06-15]
OMIM:600193	Waardenburg syndrome, type IIB		HP:0001100	PMID:7951321	PCS		36/36			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:600193	Waardenburg syndrome, type IIB		HP:0002211	PMID:7951321	PCS		36/36			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:600193	Waardenburg syndrome, type IIB		HP:0000407	PMID:7951321	PCS		36/36			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:600193	Waardenburg syndrome, type IIB		HP:0000506	PMID:7951321	PCS		0/36			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:600193	Waardenburg syndrome, type IIB		HP:0001999	PMID:7951321	PCS		0/36			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:600193	Waardenburg syndrome, type IIB		HP:0002216	PMID:7951321	PCS		36/36			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:600193	Waardenburg syndrome, type IIB		HP:0000006	PMID:7951321	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2024-03-09]
OMIM:607373	Autism, susceptibility to, 8		HP:0000750	OMIM:607373	IEA					P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0002353	OMIM:607373	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0001250	OMIM:607373	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0003144	OMIM:607373	IEA		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0011463	OMIM:607373	IEA					C	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0000717	OMIM:607373	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0000728	OMIM:607373	IEA					P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0000723	OMIM:607373	TAS					P	HPO:skoehler[2013-06-04]
OMIM:607373	Autism, susceptibility to, 8		HP:0000733	OMIM:607373	TAS					P	HPO:skoehler[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0001426	OMIM:607373	IEA					I	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0000758	OMIM:607373	IEA					P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0003745	OMIM:607373	IEA					I	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0000721	OMIM:607373	IEA					P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0000732	OMIM:607373	IEA					P	HPO:iea[2009-02-17]
OMIM:607373	Autism, susceptibility to, 8		HP:0001249	OMIM:607373	IEA					P	HPO:iea[2009-02-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001298	PMID:30245030	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002300	OMIM:618253	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002465	PMID:30245030	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002344	PMID:30245030	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0003577	PMID:30245030	PCS		1/4			C	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001250	PMID:30245030	PCS		2/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0003593	PMID:30245030	PCS		1/4			C	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001290	PMID:30245030	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0011951	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0008070	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0012179	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0011463	PMID:30245030	PCS		1/4			C	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0000737	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001987	PMID:30245030	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001943	PMID:30245030	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002119	PMID:30245030	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001942	PMID:30245030	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0003128	PMID:30245030	PCS		2/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0008936	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001562	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002015	PMID:30245030	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002133	PMID:30245030	PCS		2/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001321	PMID:30245030	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0011968	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002110	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001260	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001263	PMID:30245030	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002151	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002490	PMID:30245030	PCS		2/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002093	PMID:30245030	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0011923	PMID:30245030	PCS					P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0034295	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0033044	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001518	PMID:30245030	PCS		2/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0000007	PMID:30245030	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0000648	PMID:30245030	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002505	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001511	PMID:30245030	PCS		2/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0000047	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001257	PMID:30245030	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0002104	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0001875	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33		HP:0009879	PMID:30245030	PCS		1/4			P	HPO:probinson[2022-10-17]
OMIM:146160	Hypomelia with mullerian duct anomalies		HP:0003762	OMIM:146160	IEA					P	HPO:iea[2009-02-17]
OMIM:146160	Hypomelia with mullerian duct anomalies		HP:0001162	OMIM:146160	IEA					P	HPO:iea[2009-02-17]
OMIM:146160	Hypomelia with mullerian duct anomalies		HP:0008740	OMIM:146160	IEA					P	HPO:iea[2009-02-17]
OMIM:146160	Hypomelia with mullerian duct anomalies		HP:0001171	OMIM:146160	IEA					P	HPO:iea[2009-02-17]
OMIM:146160	Hypomelia with mullerian duct anomalies		HP:0000006	OMIM:146160	IEA					I	HPO:iea[2009-02-17]
OMIM:612018	Cataract, juvenile, with microcornea and glucosuria		HP:0003621	PMID:18304496	PCS					C	HPO:probinson[2024-03-14]
OMIM:612018	Cataract, juvenile, with microcornea and glucosuria		HP:0000518	PMID:18304496	PCS	HP:0003621	11/14			P	HPO:probinson[2013-01-09];HPO:probinson[2021-09-20]
OMIM:612018	Cataract, juvenile, with microcornea and glucosuria		HP:0000482	PMID:18304496	PCS		11/14			P	HPO:probinson[2013-04-03];HPO:probinson[2021-09-20]
OMIM:612018	Cataract, juvenile, with microcornea and glucosuria		HP:0003076	PMID:18304496	PCS		9/14			P	HPO:probinson[2013-04-03];HPO:probinson[2021-09-20]
OMIM:612018	Cataract, juvenile, with microcornea and glucosuria		HP:0000006	PMID:18304496	PCS					I	HPO:probinson[2013-04-03]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000252	PMID:7264357	PCS		0/1			P	HPO:probinson[2012-08-01];HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000992	PMID:7264357	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0004334	OMIM:278750	TAS					P	HPO:probinson[2009-02-17]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0002860	PMID:36308448	PCS		4/10			P	HPO:probinson[2012-03-03];HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000491	OMIM:278750	TAS					P	HPO:probinson[2009-02-17]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0002671	PMID:36308448	PCS		2/10			P	HPO:probinson[2012-03-03];HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0003593	PMID:7264357	PCS		1/1			C	HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0034697	PMID:7264357	PCS		1/1			P	HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0012056	PMID:36308448	PCS		0/10			P	HPO:probinson[2012-08-01];HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000509	OMIM:278750	TAS					P	HPO:probinson[2009-02-17]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000613	OMIM:278750	TAS					P	HPO:probinson[2009-02-17]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000007	PMID:10385124	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000656	OMIM:278750	TAS					P	HPO:probinson[2009-02-17]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0001510	PMID:7264357	PCS		0/1			P	HPO:probinson[2012-08-01];HPO:probinson[2023-06-10]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0001029	OMIM:278750	TAS					P	HPO:probinson[2009-02-17]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0000621	OMIM:278750	TAS					P	HPO:probinson[2009-02-17]
OMIM:278750	Xeroderma pigmentosum, variant type		HP:0007603	PMID:36308448	PCS		10/10			P	HPO:probinson[2023-06-10]
OMIM:114140	Callosities, hereditary painful		HP:0000006	OMIM:114140	IEA					I	HPO:iea[2009-02-17]
OMIM:114140	Callosities, hereditary painful		HP:0000951	OMIM:114140	IEA					P	HPO:iea[2009-02-17]
OMIM:615777	Desbuquois dysplasia 2		HP:0000286	PMID:24581741	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0003510	PMID:24581741	PCS		7/7			P	HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0001252	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0004482	OMIM:615777	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615777	Desbuquois dysplasia 2		HP:0010049	PMID:24581741	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000280	PMID:24581741	PCS		2/7			P	HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0002938	PMID:24581741	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0011461	PMID:24581741	PCS		7/7			C	HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000954	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000678	OMIM:615777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0008897	PMID:24581741	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0001769	OMIM:615777	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615777	Desbuquois dysplasia 2		HP:0002656	PMID:24581741	PCS		7/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0001763	PMID:24581741	PCS		1/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000311	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0001840	PMID:22711505	PCS					P	HPO:probinson[2024-08-04]
OMIM:615777	Desbuquois dysplasia 2		HP:0001249	PMID:24581741	PCS		5/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0003048	OMIM:615777	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0000175	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000252	OMIM:615777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0002673	OMIM:615777	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615777	Desbuquois dysplasia 2		HP:0001382	PMID:24581741	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0001263	PMID:24581741	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0002827	PMID:24581741	PCS		3/7			P	HPO:probinson[2021-05-11];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000926	PMID:24581741	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000767	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000007	PMID:24581741	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000768	PMID:24581741	PCS		1/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000520	PMID:24581741	PCS		7/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0003016	PMID:24581741	PCS		7/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000343	PMID:24581741	PCS		1/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0033102	PMID:24581741	PCS		5/7			P	HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0012725	OMIM:615777	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0012368	PMID:24581741	PCS		7/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:6000816	PMID:27030147	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:615777	Desbuquois dysplasia 2		HP:0000774	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0001863	PMID:24581741	PCS		1/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000894	OMIM:615777	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615777	Desbuquois dysplasia 2		HP:0009803	OMIM:615777	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615777	Desbuquois dysplasia 2		HP:0004976	PMID:24581741	PCS		6/7			P	HPO:probinson[2021-05-11];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0003026	PMID:24581741	PCS		7/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000750	OMIM:615777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0002970	OMIM:615777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0031936	PMID:24581741	PCS		2/7			P	HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0004233	PMID:24581741	PCS		7/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000193	OMIM:615777	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0000592	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000470	PMID:24581741	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0005280	PMID:24581741	PCS		1/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0003180	OMIM:615777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0011304	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000668	OMIM:615777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0001956	PMID:24581741	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0001511	PMID:24581741	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-11]
OMIM:615777	Desbuquois dysplasia 2		HP:0000664	OMIM:615777	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615777	Desbuquois dysplasia 2		HP:0002643	PMID:24581741	PCS	HP:0003623	4/7			P	HPO:probinson[2021-05-11]
OMIM:258480	Opsismodysplasia		HP:0002663	PMID:23273567	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:258480	Opsismodysplasia		HP:0003510	PMID:23273567	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:258480	Opsismodysplasia		HP:0004565	PMID:23273567	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0001773	PMID:23273567	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	OPSISMODYSPLASIA		HP:0003311	PMID:23273567	PCS		2/9			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0001252	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0003196	PMID:23273567	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0001290	OMIM:258480	TAS					P	HPO:skoehler[2017-07-13]
OMIM:258480	Opsismodysplasia		HP:0004482	PMID:23273567	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:258480	OPSISMODYSPLASIA		HP:0010049	PMID:23273567	PCS		9/9			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0011220	PMID:23273567	PCS		7/9			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000316	PMID:23273567	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000239	PMID:23273567	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000117	PMID:23273567	PCS		5/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000637	PMID:23273567	PCS		2/5			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000358	PMID:23273567	PCS		1/5			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000969	OMIM:258480	IEA					P	HPO:skoehler[2010-06-20]
OMIM:258480	Opsismodysplasia		HP:0000007	PMID:23273567	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000922	OMIM:258480	TAS					P	HPO:probinson[2012-06-10]
OMIM:258480	Opsismodysplasia		HP:0001538	OMIM:258480	TAS					P	HPO:probinson[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0000520	PMID:23273567	PCS		7/8			P	ORCID:0000-0002-0736-9199[2024-05-12]
OMIM:258480	Opsismodysplasia		HP:0002148	PMID:23273567	PCS		5/6			P	HPO:skoehler[2013-06-05];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000369	PMID:23273567	PCS		1/6			P	HPO:probinson[2022-05-10]
OMIM:258480	OPSISMODYSPLASIA		HP:0003577	PMID:23273567	PCS		9/9			C	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000343	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0008905	PMID:23273567	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000463	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0001591	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0003177	PMID:23273567	PCS		2/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0003175	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0003173	PMID:23273567	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	OPSISMODYSPLASIA		HP:0001270	PMID:23273567	PCS		4/6			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0008873	PMID:23273567	PCS					P	HPO:probinson[2015-02-28];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0008479	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0000774	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0001027	PMID:23273567	PCS		3/6			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000256	PMID:23273567	PCS		5/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	OPSISMODYSPLASIA		HP:0009803	PMID:23273567	PCS		9/9			P	HPO:probinson[2022-05-10]
OMIM:258480	OPSISMODYSPLASIA		HP:0002677	PMID:23273567	PCS		2/9			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0001562	PMID:23273567	PCS	HP:0011461	1/13			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0003026	PMID:23273567	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0001561	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0002650	OMIM:258480	IEA					P	HPO:skoehler[2019-09-07]
OMIM:258480	Opsismodysplasia		HP:0004279	PMID:23273567	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0003021	PMID:23273567	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0000470	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0002093	PMID:23273567	PCS		8/8			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0005280	PMID:23273567	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0003180	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0000907	OMIM:258480	TAS					P	HPO:probinson[2012-06-10]
OMIM:258480	Opsismodysplasia		HP:0000348	PMID:23273567	PCS		7/9			P	HPO:probinson[2022-05-10]
OMIM:258480	Opsismodysplasia		HP:0002007	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0002205	OMIM:258480	IEA					P	HPO:iea[2009-02-17]
OMIM:258480	Opsismodysplasia		HP:0000586	PMID:23273567	PCS		7/8			P	HPO:probinson[2022-05-10]
OMIM:615011	Phosphohydroxylysinuria		HP:6000806	PMID:23242558	PCS		3/3			P	HPO:probinson[2024-08-03];HPO:probinson[2024-08-03]
OMIM:615011	Phosphohydroxylysinuria		HP:0031870	PMID:23242558	PCS		1/1			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:615011	Phosphohydroxylysinuria		HP:0000007	PMID:23242558	PCS					I	HPO:probinson[2022-12-04]
OMIM:617606	Deafness, autosomal dominant 72		HP:0003676	PMID:28013291	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617606	Deafness, autosomal dominant 72		HP:0000407	PMID:28013291	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617606	Deafness, autosomal dominant 72		HP:0011462	PMID:28013291	PCS					C	HPO:probinson[2022-10-01]
OMIM:617606	Deafness, autosomal dominant 72		HP:0000360	PMID:28013291	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:617606	Deafness, autosomal dominant 72		HP:0000006	PMID:28013291	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-10-01]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0003577	PMID:30425301	PCS		2/2			C	HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0002231	PMID:30425301	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0008070	PMID:30425301	PCS		3/3			P	HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000958	PMID:30425301	PCS	HP:0003577	2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000613	PMID:30425301	PCS	HP:0003577	2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0002209	PMID:30425301	PCS	HP:0011463	2/2			P	HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000007	PMID:30425301	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000964	PMID:30425301	PCS		2/2			P	HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000989	PMID:30425301	PCS		1/2			P	HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000966	PMID:30425301	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000653	PMID:30425301	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000498	PMID:30425301	PCS	HP:0003577	2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0002217	PMID:30425301	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-19]
OMIM:618535	Ectodermal dysplasia 15, Hypohidrotic/hair type		HP:0000982	PMID:30425301	PCS		0/2			P	HPO:probinson[2022-10-19]
OMIM:300833	46,xx sex reversal 3		HP:0012245	PMID:21183788	PCS		3/3			P	HPO:probinson[2013-04-02];HPO:probinson[2023-04-02]
OMIM:300833	46,xx sex reversal 3		HP:0001423	PMID:21183788	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2023-04-02]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0003027	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0001773	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0008905	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0001156	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0001162	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0010049	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0000007	OMIM:611263	IEA					I	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0000774	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611263	Asphyxiating thoracic dystrophy 2		HP:0001169	OMIM:611263	IEA					P	HPO:skoehler[2010-06-19]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001892	OMIM:602579	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001399	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0002243	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001395	PMID:11134235	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001252	PMID:11134235	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001394	PMID:11134235	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0002240	PMID:11134235	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0003593	PMID:11134235	PCS		2/2			C	HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001290	OMIM:602579	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0003073	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0031842	OMIM:602579	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001929	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001508	PMID:11134235	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0000114	PMID:11134235	PCS		1/2			P	HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0002014	PMID:11134235	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0003642	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0002013	PMID:11134235	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:6000782	PMID:9525984	PCS		1/1			P	HPO:probinson[2024-06-29]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0002570	PMID:11134235	PCS		2/2			P	HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0000969	PMID:11134235	PCS		1/2			P	HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0003819	PMID:11134235	PCS		1/2			C	HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0000825	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0011473	PMID:11134235	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001977	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0000107	PMID:11134235	PCS		2/2			P	HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0000007	PMID:11134235	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:602579	Congenital disorder of glycosylation, type Ib		HP:0001976	OMIM:602579	IEA					P	HPO:iea[2009-02-17]
OMIM:186350	Syndactyly-Polydactyly-Earlobe syndrome		HP:0001177	OMIM:186350	TAS					P	HPO:probinson[2013-03-24]
OMIM:186350	Syndactyly-Polydactyly-Earlobe syndrome		HP:0000363	OMIM:186350	TAS					P	HPO:probinson[2013-03-24]
OMIM:186350	Syndactyly-Polydactyly-Earlobe syndrome		HP:0001837	OMIM:186350	TAS					P	HPO:probinson[2013-03-24]
OMIM:186350	Syndactyly-Polydactyly-Earlobe syndrome		HP:0001841	OMIM:186350	TAS					P	HPO:probinson[2013-03-24]
OMIM:186350	Syndactyly-Polydactyly-Earlobe syndrome		HP:0000006	OMIM:186350	IEA					I	HPO:iea[2009-02-17]
OMIM:186350	Syndactyly-Polydactyly-Earlobe syndrome		HP:0005767	OMIM:186350	IEA					P	HPO:iea[2009-02-17]
OMIM:186350	Syndactyly-Polydactyly-Earlobe syndrome		HP:0001853	OMIM:186350	TAS					P	HPO:probinson[2013-03-24]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0000709	PMID:23086396	PCS		HP:0040283			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-11-07]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0000708	PMID:23086396	PCS		10/15			P	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0003621	PMID:23086396	PCS					C	HPO:probinson[2022-11-07]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0002133	OMIM:615005	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0000716	OMIM:615005	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0011463	PMID:23086396	PCS					C	HPO:probinson[2022-11-07]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0000718	PMID:23086396	PCS		HP:0040283			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-11-07]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0012075	OMIM:615005	TAS		HP:0040283			P	HPO:skoehler[2013-01-21]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0007359	OMIM:615005	IEA					P	HPO:skoehler[2013-01-11]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0000006	PMID:23086396	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2022-11-07]
OMIM:615005	Epilepsy, nocturnal frontal lobe, 5		HP:0001249	PMID:23086396	PCS		6/15			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-11-07]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0001320	PMID:24702957	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0002521	PMID:24702957	PCS		1/2			P	HPO:skoehler[2014-08-24]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0001344	PMID:24702957	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0005445	PMID:24702957	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0002365	PMID:24702957	PCS		1/2			P	HPO:skoehler[2014-08-24]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0002079	PMID:24702957	PCS		1/2			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0001250	PMID:24702957	PCS		2/2			P	HPO:skoehler[2014-08-24]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0001252	PMID:24702957	PCS		1/2			P	HPO:skoehler[2014-11-26]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0003593	PMID:24702957	PCS		2/2			C	HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0001290	PMID:24702957	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0010841	PMID:24702957	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0011344	PMID:24702957	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0012469	PMID:24702957	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0034295	PMID:24702957	PCS		1/2			P	HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0002539	PMID:24702957	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0002119	PMID:24702957	PCS		1/2			P	HPO:skoehler[2014-08-24]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0000006	PMID:24702957	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-04]
OMIM:615763	Cortical dysplasia, complex, with other brain malformations 5		HP:0009879	PMID:24702957	PCS		1/2			P	HPO:skoehler[2014-11-26]
OMIM:154570	Mannose 6-phosphate receptor recognition defect, Lebanese type		HP:0004356	OMIM:154570	IEA					P	HPO:iea[2015-05-23]
OMIM:154570	Mannose 6-phosphate receptor recognition defect, Lebanese type		HP:0000006	OMIM:154570	IEA					I	HPO:iea[2009-02-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0000670	OMIM:613312	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0003621	PMID:20137773	PCS		4/5			C	HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0002970	PMID:20137773	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0004322	PMID:20137773	PCS		4/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0002750	OMIM:613312	IEA					P	HPO:skoehler[2019-04-18]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0002673	PMID:20137773	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0012408	PMID:20137773	PCS		1/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0003155	PMID:20137773	PCS		4/5			P	HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0011463	PMID:20137773	PCS		1/5			C	HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0000007	PMID:20137773	PCS					I	HPO:skoehler[2013-01-10];HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0003109	OMIM:613312	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0002857	OMIM:613312	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0004912	PMID:20137773	PCS		5/5			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-08-17]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0001642	OMIM:613312	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613312	Hypophosphatemic rickets, autosomal recessive, 2		HP:0000685	OMIM:613312	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0034518	PMID:27745832	PCS		26/28			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0002650	PMID:27745832	PCS		14/51			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0000023	PMID:27745832	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0003003	PMID:27745832	PCS		2/36			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0001030	PMID:27745832	PCS		44/52			P	HPO:skoehler[2017-07-13]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0001382	PMID:27745832	PCS		38/56			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0001373	PMID:27745832	PCS		43/53			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0030816	PMID:27745832	PCS		61/65			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0034517	PMID:27745832	PCS		50/76			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0002829	PMID:27745832	PCS		13/39			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0000704	PMID:27745832	PCS		75/83			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0001537	PMID:27745832	PCS		3/45			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0000987	PMID:27745832	PCS		29/55			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0000978	PMID:27745832	PCS		58/63			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0002667	PMID:27745832	PCS		1/36			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0001015	PMID:27745832	PCS		14/42			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0000006	PMID:27745832	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0000974	PMID:27745832	PCS		38/54			P	HPO:probinson[2023-02-19]
OMIM:617174	Ehlers-Danlos syndrome, periodontal type, 2		HP:0000225	PMID:27745832	PCS		51/58			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0001265	OMIM:618247	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0002059	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0002015	OMIM:618247	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0002353	OMIM:618247	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0000365	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0001266	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0001332	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0001272	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0003693	OMIM:618247	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0001260	OMIM:618247	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0002151	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0032653	PMID:22114105	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0002093	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0011923	PMID:22114105	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0034295	PMID:22114105	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0002509	OMIM:618247	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0000007	PMID:22114105	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0003648	PMID:22114105	PCS		1/1			P	HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0000510	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0001942	PMID:22114105	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:618247	Mitochondrial complex I deficiency, nuclear type 26		HP:0003623	PMID:22114105	PCS		1/1			C	HPO:probinson[2022-11-27]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0001265	OMIM:614455	TAS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0003774	PMID:22187985	PCS		11/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0003676	PMID:22187985	PCS					C	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0003621	PMID:22187985	PCS		5/12			C	HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0003236	PMID:22187985	PCS		5/11			P	HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0003376	OMIM:614455	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0001761	PMID:22187985	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0000097	OMIM:614455	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0003383	PMID:22187985	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0001284	PMID:22187985	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0002460	PMID:22187985	PCS		12/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0000093	PMID:22187985	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0034337	OMIM:614455	TAS					P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0000407	PMID:22187985	PCS		4/12			P	HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0011462	PMID:22187985	PCS		7/12			C	HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0009027	OMIM:614455	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0009830	PMID:22187985	PCS		12/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0002936	OMIM:614455	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0007149	PMID:22187985	PCS		12/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0000006	PMID:22187985	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0003447	PMID:22187985	PCS		6/6			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0008944	PMID:22187985	PCS		12/12			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-10]
OMIM:614455	Charcot-Marie-Tooth disease, dominant intermediate E		HP:0001765	OMIM:614455	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000110	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0003774	PMID:22626039	PCS	HP:0003621	2/2			P	HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000365	OMIM:615993	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0004322	PMID:22626039	PCS		2/2			P	HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0002098	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000083	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0001263	PMID:22626039	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0003241	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0010442	PMID:22626039	PCS		0/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0011950	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0100543	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000107	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000007	PMID:20835237	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000403	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000546	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0007663	PMID:22626039	PCS		2/2			P	HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0002205	PMID:22626039	PCS		1/2		HP:0011010	P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000510	PMID:22626039	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000135	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0001249	PMID:22626039	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0001513	PMID:22626039	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-25]
OMIM:615993	Bardet-Biedl syndrome 16		HP:0000104	OMIM:615993	TAS					P	HPO:skoehler[2014-11-26]
OMIM:609404	Preeclampsia/eclampsia 4		HP:0100601	OMIM:609404	IEA					H	HPO:skoehler[2015-01-27]
OMIM:609404	Preeclampsia/eclampsia 4		HP:0100602	PMID:17290274	PCS					H	HPO:probinson[2013-01-09]
OMIM:609404	Preeclampsia/eclampsia 4		HP:0011462	PMID:17290274	PCS					C	HPO:probinson[2022-03-31]
OMIM:609404	Preeclampsia/eclampsia 4		HP:0010982	PMID:17290274	PCS					I	HPO:probinson[2013-03-26]
OMIM:107100	Anorectal anomalies		HP:0000143	OMIM:107100	IEA					P	HPO:iea[2009-02-17]
OMIM:107100	Anorectal anomalies		HP:0002023	OMIM:107100	IEA					P	HPO:iea[2009-02-17]
OMIM:107100	Anorectal anomalies		HP:0000006	OMIM:107100	IEA					I	HPO:iea[2009-02-17]
OMIM:614333	Intellectual developmental disorder, autosomal recessive 29		HP:0001344	PMID:21629298	PCS		5/5			P	HPO:probinson[2018-06-13];HPO:probinson[2024-03-15]
OMIM:614333	Intellectual developmental disorder, autosomal recessive 29		HP:0001252	PMID:21629298	PCS					P	HPO:probinson[2018-06-13]
OMIM:614333	Intellectual developmental disorder, autosomal recessive 29		HP:0000717	PMID:21629298	PCS		0/5			P	HPO:probinson[2018-06-13];HPO:probinson[2024-03-15]
OMIM:614333	Intellectual developmental disorder, autosomal recessive 29		HP:0000007	PMID:21629298	PCS					I	HPO:skoehler[2017-07-13]
OMIM:614333	Intellectual developmental disorder, autosomal recessive 29		HP:0001270	PMID:21629298	PCS				HP:0012825	P	HPO:probinson[2018-06-13]
OMIM:614327	Tumor predisposition syndrome		HP:0012056	PMID:21941004;PMID:21874003	PCS		5/23			P	HPO:probinson[2022-04-17];HPO:skoehler[2012-10-17];HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0007716	PMID:21941004;PMID:21874003	PCS		4/23			P	HPO:probinson[2022-04-17];HPO:skoehler[2012-10-17];HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0003596	PMID:21874003	PCS		3/8			C	HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0003584	PMID:21874003	PCS		1/8			C	HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0030078	PMID:21941004	PCS		1/8			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0005584	OMIM:614327	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614327	Tumor predisposition syndrome		HP:0011462	PMID:21874003	PCS		4/8			C	HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0002858	PMID:21941004	PCS		1/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0000006	PMID:21874003	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-17]
OMIM:614327	Tumor predisposition syndrome		HP:0100001	PMID:21941004	PCS		1/8			P	HPO:probinson[2022-04-17]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0003774	PMID:31481669	PCS	HP:0011463	11/11			P	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000341	PMID:31481669	PCS		3/8			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0002036	PMID:31481669	PCS		3/11			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000252	PMID:31481669	PCS		11/11			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0001266	PMID:31481669	PCS		1/11			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0001272	PMID:31481669	PCS		9/9			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0002120	PMID:31481669	PCS		9/9			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0001263	PMID:31481669	PCS		11/11			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000097	PMID:31481669	PCS		3/6			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0003593	PMID:31481669	PCS		7/11			C	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0005484	PMID:31481669	PCS		10/11			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0002020	PMID:31481669	PCS		3/11			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0033725	PMID:31481669	PCS		5/9			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0011463	PMID:31481669	PCS		4/11			C	HPO:probinson[2022-02-01];HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000316	PMID:31481669	PCS		1/8			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000007	PMID:31481669	PCS					I	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000601	PMID:31481669	PCS		2/8			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0002119	PMID:31481669	PCS		5/9			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0007874	PMID:31481669	PCS		3/8			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0002208	PMID:31481669	PCS		2/8			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0001967	PMID:31481669	PCS		3/6			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000400	PMID:31481669	PCS		3/8			P	HPO:probinson[2022-02-01]
OMIM:619603	Galloway-Mowat syndrome 9		HP:0000369	PMID:31481669	PCS		3/8			P	HPO:probinson[2022-02-01]
OMIM:193007	Vestibulopathy, familial		HP:0000365	PMID:8290084	PCS		0/3			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-08]
OMIM:193007	Vestibulopathy, familial		HP:0002321	PMID:8290084	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-08]
OMIM:193007	Vestibulopathy, familial		HP:0034773	PMID:8290084	PCS		3/3			P	HPO:probinson[2024-03-08]
OMIM:193007	Vestibulopathy, familial		HP:0002141	PMID:8290084	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:193007	Vestibulopathy, familial		HP:0000006	PMID:8290084	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:193007	Vestibulopathy, familial		HP:0003677	PMID:8290084	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003236	PMID:28821231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002067	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001332	PMID:28821231;PMID:15911822;PMID:12510040	PCS		66/67			P	ORCID:0000-0002-0736-9199[2024-05-04];HPO:iea[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003198	OMIM:234200	TAS					P	HPO:skoehler[2012-11-18]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001250	PMID:28821231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003199	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003155	PMID:28821231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002063	PMID:28821231;PMID:15911822;PMID:12510040	PCS		60/67			P	ORCID:0000-0002-0736-9199[2024-05-04];HPO:iea[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001251	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003593	PMID:15911822	PCS		2/16			C	HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002180	OMIM:234200	TAS					P	HPO:probinson[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000716	PMID:28821231;PMID:15911822	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-05-04];HPO:probinson[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0008770	PMID:15911822	PCS		7/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0011463	PMID:28821231;PMID:15911822	PCS		4/15			C	ORCID:0000-0002-0736-9199[2024-05-04];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0011462	PMID:15911822	PCS		2/14			C	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001927	PMID:15911822;PMID:12510040	PCS		6/66			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-14];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000953	OMIM:234200	TAS					P	HPO:probinson[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000752	PMID:15911822	PCS		4/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001249	PMID:28821231	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002311	PMID:28821231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001300	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003487	PMID:12510040	PCS		13/52			P	HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001266	PMID:12510040	PCS		51/52			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002310	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001260	PMID:15911822;PMID:12510040	PCS		65/66			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001263	PMID:15911822;PMID:12510040	PCS		5/34			P	ORCID:0000-0002-0736-9199[2024-05-04];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002072	PMID:28821231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002071	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001618	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000726	PMID:15911822;OMIM:234200	PCS		11/24			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000007	PMID:15911822	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000648	PMID:15911822;PMID:12510040	PCS		3/80			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0007313	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002505	PMID:15911822	PCS		5/14			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002304	PMID:15911822	PCS		2/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001257	PMID:12510040	PCS		13/52			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001337	PMID:15911822	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000643	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003678	OMIM:234200	TAS					C	HPO:skoehler[2012-11-26]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002120	PMID:28821231	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002283	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000020	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000580	PMID:15911822	PCS		4/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0100035	PMID:15911822	PCS		1/14			P	HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0100034	PMID:15911822	PCS		2/14			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0008872	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000658	OMIM:234200	TAS					P	HPO:probinson[2012-07-16]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001268	PMID:15911822;PMID:12510040	PCS		25/68			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001347	PMID:12510040	PCS		13/52			P	HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002454	PMID:28821231;PMID:15911822	PCS		15/15			P	ORCID:0000-0002-0736-9199[2024-05-04];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0002015	PMID:15911822	PCS		5/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0003621	PMID:15911822	PCS		9/14			C	HPO:probinson[2022-03-14]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0031814	OMIM:234200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0001288	PMID:15911822;OMIM:234200	PCS		18/18			P	HPO:iea[2009-02-17];ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000273	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0007256	PMID:15911822	PCS		12/14			P	HPO:skoehler[2015-01-04];HPO:probinson[2024-05-04]
OMIM:234200	Neurodegeneration with brain iron accumulation 1		HP:0000546	OMIM:234200	IEA					P	HPO:iea[2009-02-17]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0025452	PMID:27030597;PMID:28835462	PCS		11/13			P	HPO:probinson[2020-08-13];HPO:probinson[2020-11-27]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0003565	PMID:28835462	PCS		1/3			P	HPO:probinson[2020-11-27]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0030783	PMID:27030597	PCS					P	HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0011944	PMID:27030597	PCS					P	HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0010783	PMID:27030597	PCS					P	HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0011227	PMID:27030597;PMID:28835462	PCS		11/13			P	HPO:probinson[2020-08-13];HPO:probinson[2020-11-27]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0002829	PMID:27030597	PCS		12/12			P	HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0040154	PMID:28835462	PCS		1/3			P	HPO:probinson[2020-11-27]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0001903	PMID:27030597	PCS		4/12			P	HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0011463	PMID:27030597	PCS					C	HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0033188	PMID:28835462	PCS		3/3			P	HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0001954	PMID:27030597;PMID:28835462	PCS		13/15			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-11-27]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0012490	PMID:28835462	PCS		1/3			P	HPO:probinson[2020-11-27]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0000006	PMID:27030597	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0003326	PMID:27030597	PCS		12/12			P	HPO:probinson[2020-08-13]
OMIM:608068	Neutrophilic dermatosis, acute febrile		HP:0001644	PMID:27030597	PCS		1/12			P	HPO:probinson[2020-08-13]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0003577	PMID:33100333	PCS		1/1			C	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0005599	PMID:33100333	PCS		2/2			P	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0000639	PMID:33100333	PCS		2/2			P	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0012805	PMID:33100333	PCS		2/2			P	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0001010	PMID:33100333	PCS		2/2			P	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0000613	PMID:33100333	PCS		1/2			P	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0007750	PMID:33100333	PCS		1/2			P	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0000007	PMID:33100333	PCS					I	HPO:probinson[2021-03-07];HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0007663	PMID:33100333	PCS		2/2			P	HPO:probinson[2021-03-07]
OMIM:619165	Oculocutaneous albinism, type VIII		HP:0040030	PMID:33100333	PCS		2/2			P	HPO:probinson[2021-03-07]
OMIM:609376	Cataract 35		HP:0000518	OMIM:609376	IEA					P	HPO:skoehler[2015-01-27]
OMIM:609376	Cataract 35		HP:0000007	OMIM:609376	TAS					I	HPO:skoehler[2014-01-28]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0030314	OMIM:614441	PCS					P	HPO:skoehler[2015-04-05]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0003621	PMID:23509104	PCS		2/5			C	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0001051	PMID:23509104	PCS		5/7			P	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0003073	PMID:23509104	PCS		3/7			P	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0030839	PMID:23509104	PCS		5/7			P	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0001072	PMID:23509104	PCS		5/7			P	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0001061	PMID:23509104	PCS		5/7			P	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0100774	OMIM:614441	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0011462	PMID:23509104	PCS		3/5			C	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0000007	PMID:23509104	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0001217	PMID:23509104	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0000975	PMID:23509104	PCS		1/7			P	HPO:probinson[2021-07-10]
OMIM:614441	Hypertrophic osteoarthropathy, primary, autosomal recessive 2		HP:0005208	PMID:23509104	PCS		7/7			P	HPO:probinson[2021-07-10]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0001250	PMID:34900151	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0000083	OMIM:615987	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0001263	PMID:34900151	PCS		1/1			P	HPO:probinson[2023-02-18]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0000107	OMIM:615987	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0000007	PMID:16582908	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-18]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0010442	PMID:34900151	PCS		0/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-18]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0000510	PMID:34900151	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-18]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0000135	OMIM:615987	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0001513	PMID:34900151	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-18]
OMIM:615987	Bardet-Biedl syndrome 10		HP:0000556	PMID:34900151	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-18]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001276	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0002883	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001254	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001596	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001992	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0002013	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001250	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001263	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001252	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001290	OMIM:253270	TAS					P	HPO:skoehler[2017-07-13]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0000737	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:4000200	PMID:8319716	PCS		1/1			P	HPO:probinson[2024-01-06]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0033596	PMID:8319716	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0033111	PMID:8319716	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0000007	PMID:7842009	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0008872	PMID:8319716	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001987	PMID:8319716	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0000988	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0002789	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001873	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001942	PMID:8319716	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-25]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0001259	OMIM:253270	IEA					P	HPO:iea[2009-02-17]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0003623	PMID:8319716	PCS		1/1			C	HPO:probinson[2023-02-25]
OMIM:253270	Holocarboxylase synthetase deficiency		HP:0003128	PMID:8319716	PCS		1/1			P	HPO:probinson[2023-02-25]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0003038	OMIM:201250	TAS		20/20			P	HPO:skoehler[2010-06-20];HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0001773	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0003022	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0003042	OMIM:201250	TAS					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0003086	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0005096	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0008890	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002827	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0006011	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0006110	OMIM:201250	TAS					P	HPO:iea[2012-06-09]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0000954	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0006144	OMIM:201250	TAS					P	HPO:iea[2012-06-09]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0000007	OMIM:201250	IEA					I	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0006014	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002986	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0005736	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0009778	OMIM:201250	TAS					P	HPO:iea[2009-02-17]
OMIM:201250	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002984	OMIM:201250	IEA					P	HPO:iea[2009-02-17]
OMIM:612965	46XY sex reversal 3		HP:0000808	PMID:17200175	PCS	HP:0003577	1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0000013	OMIM:612965	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612965	46XY sex reversal 3		HP:0000133	PMID:17200175	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0012245	PMID:17200175	PCS		2/4			P	HPO:skoehler[2015-01-27];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0001470	PMID:17200175	PCS					I	HPO:probinson[2013-04-07];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0000062	PMID:17200175	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0011969	PMID:17200175	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0008232	PMID:17200175	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0008665	PMID:17200175	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-30]
OMIM:612965	46XY sex reversal 3		HP:0030913	PMID:17200175	PCS		1/4			P	HPO:probinson[2020-11-30]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0005479	PMID:30063982	PCS		1/1			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0010803	PMID:28532655	PCS		2/2			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0410297	PMID:28532655	PCS		1/1			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0410395	PMID:28532655	PCS		1/1			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0003593	PMID:28532655	PCS		1/2			C	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0011240	PMID:28532655	PCS		2/2			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0001508	PMID:28532655	PCS		1/2			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0002719	PMID:28532655	PCS		1/2			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0011463	PMID:28532655;PMID:30063982	PCS		2/3			C	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0001903	PMID:30063982	PCS		1/1			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0000316	PMID:28532655	PCS		2/2			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0006532	PMID:28532655;PMID:30063982	PCS		2/3			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0004812	PMID:28532655	PCS		1/2			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0001744	PMID:28532655	PCS		1/2			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0004315	PMID:28532655;PMID:30063982	PCS		2/3			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0500266	PMID:28532655	PCS		1/1			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0000396	PMID:28532655	PCS		2/2			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0002850	PMID:28532655;PMID:30063982	PCS		3/3			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0004432	PMID:28532655	PCS		1/2			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0005280	PMID:28532655	PCS		2/2			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0010976	PMID:28532655;PMID:30063982	PCS		3/3			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0000007	PMID:28532655	PCS					I	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0000322	PMID:28532655	PCS		2/2			P	HPO:probinson[2022-06-27];HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0001876	PMID:28532655	PCS		1/2			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0002720	PMID:28532655;PMID:30063982	PCS		3/3			P	HPO:probinson[2022-06-27]
OMIM:619824	Agammaglobulinemia 8B, autosomal recessive		HP:0002028	PMID:30063982	PCS		1/1			P	HPO:probinson[2022-06-27]
OMIM:617809	Geleophysic dysplasia 3		HP:0000343	OMIM:617809	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617809	Geleophysic dysplasia 3		HP:0001773	OMIM:617809	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617809	Geleophysic dysplasia 3		HP:0000463	PMID:27068007	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0001156	PMID:27068007	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0004322	PMID:27068007	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0002240	PMID:27068007	PCS		0/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0001072	OMIM:617809	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617809	Geleophysic dysplasia 3		HP:0001607	PMID:27068007	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0011463	PMID:27068007	PCS		2/3			C	HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0001609	PMID:27068007	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0012471	PMID:27068007	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0000414	PMID:27068007	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0002878	OMIM:617809	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617809	Geleophysic dysplasia 3		HP:0002656	OMIM:617809	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617809	Geleophysic dysplasia 3		HP:0002777	OMIM:617809	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617809	Geleophysic dysplasia 3		HP:0000311	PMID:27068007	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0002996	PMID:27068007	PCS		2/3			P	HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0003623	PMID:27068007	PCS		1/3			C	HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0001622	PMID:27068007	PCS		1/3			P	HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0009826	OMIM:617809	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617809	Geleophysic dysplasia 3		HP:0001561	OMIM:617809	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617809	Geleophysic dysplasia 3		HP:0000431	PMID:27068007	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0002750	OMIM:617809	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617809	Geleophysic dysplasia 3		HP:0000293	PMID:27068007	PCS		1/3			P	HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0002094	OMIM:617809	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617809	Geleophysic dysplasia 3		HP:0002090	OMIM:617809	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617809	Geleophysic dysplasia 3		HP:0005280	PMID:27068007	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0010535	OMIM:617809	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617809	Geleophysic dysplasia 3		HP:0006248	PMID:27068007	PCS		2/3			P	HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0001653	PMID:27068007	PCS		1/3			P	HPO:probinson[2023-02-06]
OMIM:617809	Geleophysic dysplasia 3		HP:0000006	PMID:27068007	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-06]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0000253	OMIM:608097	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0000252	OMIM:608097	TAS					P	HPO:skoehler[2014-01-28]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0002521	OMIM:608097	TAS					P	HPO:skoehler[2014-01-28]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0002079	OMIM:608097	TAS					P	HPO:skoehler[2014-01-28]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0001250	PMID:12682315	PCS					P	HPO:probinson[2013-03-24]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0001263	PMID:12682315	PCS					P	HPO:probinson[2013-03-24]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0001252	OMIM:608097	TAS					P	HPO:skoehler[2014-11-26]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0003593	OMIM:608097	TAS					C	HPO:skoehler[2014-01-28]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0002273	OMIM:608097	TAS					P	HPO:skoehler[2014-01-28]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0001290	OMIM:608097	TAS					P	HPO:skoehler[2017-07-13]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0032388	OMIM:608097	IEA					P	HPO:skoehler[2019-09-07]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0001508	OMIM:608097	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0007165	PMID:12682315	PCS					P	HPO:probinson[2013-03-24]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0000817	OMIM:608097	TAS					P	HPO:skoehler[2014-01-28]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0000007	PMID:12682315	PCS					I	HPO:probinson[2013-01-09]
OMIM:608097	Periventricular heterotopia with microcephaly, autosomal recessive		HP:0001249	OMIM:608097	TAS				HP:0012828	P	HPO:skoehler[2014-01-28]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0001276	OMIM:618284	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0004325	PMID:27582084	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0000252	PMID:27582084	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0003577	PMID:27582084	PCS		4/4			C	HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0000750	PMID:27582084	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0004322	PMID:27582084	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0003487	PMID:27582084	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0001332	PMID:27582084	PCS		4/4			P	HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0001260	PMID:27582084	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0002396	PMID:27582084	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0002064	PMID:27582084	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0002194	PMID:27582084	PCS		4/4			P	HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0000519	PMID:27582084	PCS	HP:0003577	4/4			P	HPO:skoehler[2019-04-18]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0000007	PMID:27582084	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0001510	PMID:27582084	PCS		4/4			P	HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0007018	PMID:27582084	PCS		4/4			P	HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0001249	PMID:27582084	PCS		4/4			P	HPO:probinson[2023-03-31]
OMIM:618284	Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum		HP:0000501	PMID:27582084	PCS		1/4			P	HPO:probinson[2023-03-31]
OMIM:615978	Immunodeficiency 27B		HP:0005661	PMID:15589309	PCS					P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:615978	Immunodeficiency 27B		HP:0011275	PMID:15589309	PCS					P	HPO:probinson[2022-04-12]
OMIM:615978	Immunodeficiency 27B		HP:0011274	PMID:15589309	PCS					P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:615978	Immunodeficiency 27B		HP:0008940	PMID:28902581	PCS					P	HPO:probinson[2017-09-17]
OMIM:615978	Immunodeficiency 27B		HP:0000006	PMID:15589309	PCS					I	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:615978	Immunodeficiency 27B		HP:0002721	PMID:15589309	PCS					P	HPO:skoehler[2015-09-15];HPO:probinson[2022-04-12]
OMIM:615978	Immunodeficiency 27B		HP:0002754	PMID:28902581	PCS					P	HPO:probinson[2017-09-17]
OMIM:610828	Holoprosencephaly 7		HP:0006988	PMID:17001668	PCS		2/4			P	HPO:probinson[2017-05-28];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0000242	OMIM:610828	TAS					P	HPO:probinson[2012-05-01]
OMIM:610828	Holoprosencephaly 7		HP:0010649	OMIM:610828	TAS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0000161	PMID:17001668;PMID:11941477	PCS		3/12			P	HPO:probinson[2023-03-12];HPO:probinson[2024-03-29]
OMIM:610828	Holoprosencephaly 7		HP:0001250	OMIM:610828	TAS					P	HPO:probinson[2017-05-28]
OMIM:610828	Holoprosencephaly 7		HP:0004122	PMID:17001668	PCS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0003196	PMID:17001668	PCS		1/4			P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0000283	PMID:18830227	PCS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0100333	PMID:17001668	PCS		2/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0010650	OMIM:610828	TAS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0003829	OMIM:610828	TAS					I	HPO:skoehler[2017-07-13]
OMIM:610828	Holoprosencephaly 7		HP:0000437	PMID:17001668	PCS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0000316	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0006870	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0000238	PMID:11941477	PCS		1/8			P	HPO:probinson[2017-05-28];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0006315	PMID:17001668;PMID:11941477	PCS		2/12			P	HPO:probinson[2023-03-12];HPO:probinson[2012-04-24];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0005469	PMID:18830227	PCS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0000175	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0000252	PMID:17001668	PCS		3/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0005104	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0011803	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0001263	PMID:17001668;PMID:11941477	PCS		7/12			P	HPO:probinson[2023-03-12];HPO:probinson[2012-04-24];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0011800	OMIM:610828	TAS					P	HPO:skoehler[2017-07-13]
OMIM:610828	Holoprosencephaly 7		HP:0100336	PMID:11941477	PCS		2/8			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0100337	PMID:11941477	PCS		1/8			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0100334	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0009099	PMID:17001668;PMID:11941477	PCS		3/12			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0009891	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0000601	PMID:17001668;PMID:11941477	PCS		5/12			P	HPO:probinson[2023-03-12];HPO:probinson[2012-04-24];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0000568	PMID:17001668	PCS		2/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0001338	PMID:11941477	PCS		1/8			P	HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0002507	OMIM:610828	TAS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0001539	PMID:11941477	PCS		1/8			P	HPO:probinson[2012-04-24];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0007633	PMID:17001668	PCS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0000400	PMID:17001668	PCS		3/4			P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0000006	PMID:11941477	PCS					I	HPO:probinson[2010-03-17]
OMIM:610828	Holoprosencephaly 7		HP:0003577	PMID:17001668;PMID:11941477	PCS		10/10			C	HPO:probinson[2023-03-12];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0000582	PMID:17001668;PMID:11941477	PCS		4/12			P	HPO:probinson[2017-05-28];HPO:probinson[2022-06-22];HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0002365	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0001274	PMID:17001668;PMID:11941477	PCS		2/12			P	HPO:probinson[2012-04-24];HPO:probinson[2023-03-12];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0005273	PMID:17001668	PCS		2/4			P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0010664	PMID:11941477	PCS		1/8			P	HPO:probinson[2017-05-28];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0012368	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0000612	PMID:17001668	PCS		1/4			P	HPO:probinson[2017-05-28]
OMIM:610828	Holoprosencephaly 7		HP:0002436	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0000256	OMIM:610828	TAS					P	HPO:probinson[2012-04-24]
OMIM:610828	Holoprosencephaly 7		HP:0000871	PMID:11941477	PCS		1/8			P	HPO:probinson[2012-04-24];HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0000431	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0001360	PMID:11941477	PCS		4/8			P	HPO:probinson[2022-06-22]
OMIM:610828	Holoprosencephaly 7		HP:0002007	OMIM:610828	TAS					P	HPO:probinson[2012-05-01]
OMIM:610828	Holoprosencephaly 7		HP:0000664	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0000267	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:610828	Holoprosencephaly 7		HP:0000586	PMID:17001668	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001298	PMID:25758935	PCS					P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0002069	PMID:25758935	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000341	PMID:25758935	PCS		2/3			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000286	PMID:25758935	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001276	PMID:27601654;PMID:25758935	PCS		13/16			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0003676	PMID:27601654	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001371	PMID:27601654	PCS		3/14			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001250	PMID:27601654	PCS		5/14			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0002121	PMID:25758935	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001252	PMID:25758935	PCS		2/3			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001252	PMID:27601654	PCS	HP:0003593	7/8			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0003593	PMID:25758935	PCS		3/3			C	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001508	PMID:25758935	PCS		1/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000218	PMID:25758935	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001249	PMID:27601654	PCS		14/14			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000358	PMID:25758935	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001347	PMID:27601654;PMID:25758935	PCS		12/15			P	HPO:probinson[2022-04-12];HPO:probinson[2022-05-31];HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000252	PMID:27601654;PMID:25758935	PCS		16/17			P	HPO:probinson[2022-04-12];HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001344	PMID:25758935	PCS		3/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0002079	PMID:27601654	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001260	PMID:27601654	PCS		10/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001263	PMID:25758935	PCS		3/3			P	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0005484	PMID:27601654	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000007	PMID:25758935	PCS					I	HPO:skoehler[2015-09-16];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000601	PMID:25758935	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0002307	PMID:27601654	PCS		11/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0001257	PMID:27601654	PCS		10/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-12]
OMIM:616281	Neurodevelopmental disorder with microcephaly and spastic paraplegia		HP:0000369	PMID:25758935	PCS		1/3			P	HPO:probinson[2022-04-12]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0002465	OMIM:245348	IEA					P	HPO:iea[2009-02-17]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0002268	PMID:16049940	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001332	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001252	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001251	PMID:16049940	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0003593	PMID:16049940	PCS		2/2			C	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001270	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0000639	PMID:16049940	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0000657	PMID:16049940	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0020045	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0007325	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001348	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001347	OMIM:245348	IEA					P	HPO:iea[2009-02-17]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0003128	OMIM:245348	IEA				HP:0012825	P	HPO:iea[2012-05-05]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0000252	OMIM:245348	IEA					P	HPO:iea[2009-02-17]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001266	PMID:16049940	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0011968	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001263	PMID:16049940;OMIM:245348	PCS		12/12			P	HPO:skoehler[2019-02-22];HPO:skoehler[2014-04-04];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0002194	OMIM:245348	IEA					P	HPO:iea[2009-02-17]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0032988	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0002928	OMIM:245348	TAS					P	HPO:skoehler[2017-07-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0012043	PMID:16049940	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0000508	PMID:16049940	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0000007	PMID:16049940	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0001319	OMIM:245348	IEA					P	HPO:iea[2009-02-17]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0002307	PMID:16049940	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:245348	Pyruvate dehydrogenase E2 deficiency		HP:0006961	PMID:16049940	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001650	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0004325	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000684	PMID:15770227	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001651	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0004322	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001371	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001250	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000482	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0010722	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0012304	PMID:15004558	PCS		1/11			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0010055	PMID:15770227	PCS		2/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000519	PMID:15004558	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000519	PMID:15770227	PCS	HP:0003577	3/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001643	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001642	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000677	PMID:15770227	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000358	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001765	PMID:15004558	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0002974	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001188	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000176	PMID:15004558	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000572	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000252	PMID:15004558	PCS		1/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000574	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0002079	PMID:15004558	PCS		1/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0004691	PMID:15004558	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000528	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000407	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0033189	PMID:15770227;PMID:15004558	PCS		8/11			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001537	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000689	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000568	PMID:15004558	PCS		9/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000568	PMID:15770227	PCS	HP:0003577	3/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000846	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001852	PMID:15770227	PCS		2/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000047	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0011090	OMIM:300166	TAS					P	HPO:skoehler[2012-10-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000343	PMID:15770227	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000541	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000581	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001153	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001270	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0040080	OMIM:300166	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300166	Microphthalmia, syndromic 2		HP:0100348	PMID:15770227	PCS		3/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001629	PMID:15004558	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001629	PMID:15770227	PCS	HP:0003577	2/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0100349	PMID:15770227	PCS		3/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0005709	PMID:15770227	PCS		1/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001305	PMID:15004558	PCS		1/11			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000612	PMID:15770227	PCS	HP:0003577	1/3			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000455	PMID:15770227;PMID:15004558	PCS		10/14			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0006335	PMID:15004558	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001423	OMIM:300166	IEA					I	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000378	PMID:15004558	PCS		1/11			P	HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0002313	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000456	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000577	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000275	OMIM:300166	TAS					P	HPO:probinson[2012-05-01]
OMIM:300166	Microphthalmia, syndromic 2		HP:0007968	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0002650	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001762	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000276	OMIM:300166	TAS					P	HPO:probinson[2012-05-01]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000193	PMID:15770227	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0011069	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001719	PMID:15004558	PCS		1/11			P	HPO:skoehler[2015-02-22];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000508	PMID:15770227	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000426	PMID:15004558	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000821	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000667	OMIM:300166	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001631	PMID:15004558	PCS		7/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:300166	Microphthalmia, syndromic 2		HP:0007733	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000028	OMIM:300166	TAS					P	HPO:skoehler[2015-02-22]
OMIM:300166	Microphthalmia, syndromic 2		HP:0000501	OMIM:300166	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300166	Microphthalmia, syndromic 2		HP:0001634	OMIM:300166	IEA					P	HPO:iea[2009-02-17]
OMIM:614496	Pseudohypoaldosteronism, type IIE		HP:0002153	OMIM:614496	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614496	Pseudohypoaldosteronism, type IIE		HP:0008242	PMID:22266938	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-03-05]
OMIM:614496	Pseudohypoaldosteronism, type IIE		HP:0004918	OMIM:614496	TAS					P	HPO:skoehler[2015-12-30]
OMIM:614496	Pseudohypoaldosteronism, type IIE		HP:0000822	PMID:22266938	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614496	Pseudohypoaldosteronism, type IIE		HP:0011423	OMIM:614496	TAS					P	HPO:skoehler[2013-01-22]
OMIM:614496	Pseudohypoaldosteronism, type IIE		HP:0000006	PMID:22266938	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:614496	Pseudohypoaldosteronism, type IIE		HP:0001942	PMID:22266938	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2023-03-05]
OMIM:133500	Exchondrosis of pinna, posterior		HP:0000598	OMIM:133500	IEA					P	HPO:iea[2009-02-17]
OMIM:133500	Exchondrosis of pinna, posterior		HP:0000006	OMIM:133500	IEA					I	HPO:iea[2009-02-17]
OMIM:612781	Growth hormone deficiency, isolated, type IB		HP:0031878	PMID:8496314	PCS		2/5			P	HPO:probinson[2023-04-09]
OMIM:612781	Growth hormone deficiency, isolated, type IB		HP:0000054	PMID:8496314	PCS		3/3	MALE		P	HPO:probinson[2023-04-09]
OMIM:612781	Growth hormone deficiency, isolated, type IB		HP:0004322	OMIM:612781	TAS		5/5			P	HPO:probinson[2013-04-07];HPO:probinson[2023-04-09]
OMIM:612781	Growth hormone deficiency, isolated, type IB		HP:0002750	OMIM:612781	TAS					P	HPO:probinson[2013-04-07]
OMIM:612781	Growth hormone deficiency, isolated, type IB		HP:0000007	PMID:8288694	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-24]
OMIM:612781	Growth hormone deficiency, isolated, type IB		HP:0034323	PMID:8496314	PCS		5/5			P	HPO:probinson[2023-04-09]
OMIM:612781	Growth hormone deficiency, isolated, type IB		HP:0000824	PMID:8496314	PCS		5/5			P	HPO:probinson[2013-04-07];HPO:probinson[2023-04-09]
OMIM:300600	Aland island eye disease		HP:0000483	PMID:17525176	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0000639	PMID:17525176	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0001141	PMID:17525176	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0007750	PMID:17525176	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0005592	PMID:17525176	PCS		0/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0007894	PMID:17525176	PCS		6/6			P	HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0011522	PMID:17525176	PCS		6/6			P	HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0001417	PMID:17525176	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:300600	Aland island eye disease		HP:0000545	PMID:17525176	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001187	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0003577	PMID:2993307	PCS		1/1			C	HPO:probinson[2022-11-04]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0002650	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001762	OMIM:617821	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001030	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001382	PMID:2993307	PCS	HP:0003577	1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-04]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001075	OMIM:617821	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001290	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0002194	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0032153	OMIM:617821	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0002808	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0002827	PMID:2993307	PCS	HP:0003577	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-04]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001822	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0000978	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0003307	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0000977	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0000015	OMIM:617821	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0002645	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001763	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0000006	PMID:2993307	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-04]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0001623	OMIM:617821	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617821	Ehlers-Danlos syndrome, arthrochalasia type, 2		HP:0000974	OMIM:617821	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300614	Deafness, X-linked 5		HP:0003202	PMID:25986071	PCS		0/16			P	HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0000365	PMID:25986071	PCS		16/16			P	HPO:probinson[2013-04-05];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0004454	PMID:25986071	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0002321	PMID:25986071	PCS		0/16			P	HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0000360	PMID:25986071	PCS		12/16			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0001284	PMID:25986071	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0003390	PMID:25986071	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0001419	PMID:25986071	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0011463	PMID:25986071	PCS		16/16			C	HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0034585	PMID:25986071	PCS		7/7			P	HPO:probinson[2023-03-31]
OMIM:300614	Deafness, X-linked 5		HP:0002936	PMID:25986071	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0002317	PMID:25986071	PCS		7/16			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0003677	PMID:25986071	PCS					C	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0000545	PMID:25986071	PCS		4/16			P	HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0001249	PMID:25986071	PCS		0/16			P	HPO:probinson[2023-02-28]
OMIM:300614	Deafness, X-linked 5		HP:0001963	PMID:25986071	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-28]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0002069	PMID:21549341	PCS		8/14			P	HPO:probinson[2022-05-15];HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0002059	OMIM:204300	IEA					P	HPO:iea[2009-02-17]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0002367	OMIM:204300	TAS					P	HPO:probinson[2012-06-11]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0003596	PMID:21549341	PCS		3/14			C	HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0002352	OMIM:204300	IEA					P	HPO:iea[2009-02-17]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0003584	PMID:21549341	PCS		1/14			C	HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0003581	OMIM:204300	IEA					C	HPO:iea[2009-02-17]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0002074	OMIM:204300	IEA					P	HPO:iea[2009-02-17]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0001251	PMID:21549341	PCS		7/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0031475	PMID:21549341	PCS		1/14			P	HPO:probinson[2022-05-15];HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0002071	OMIM:204300	IEA					P	HPO:iea[2009-02-17]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0000716	OMIM:204300	IEA					P	HPO:iea[2009-02-17]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0000726	PMID:21549341	PCS		9/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0011462	PMID:21549341	PCS		10/14			C	HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0000007	PMID:21549341	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0008765	OMIM:204300	TAS					P	HPO:probinson[2012-06-11]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0003208	OMIM:204300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0003657	OMIM:204300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0007359	PMID:21549341	PCS		2/14			P	HPO:probinson[2022-05-15];HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0001268	PMID:21549341	PCS		14/14			P	HPO:probinson[2022-05-15]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0003226	OMIM:204300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0003205	OMIM:204300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:204300	Ceroid lipofuscinosis, neuronal, 6B (Kufs type)		HP:0001336	PMID:21549341	PCS		8/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:280000	CHIME syndrome		HP:0002069	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000286	PMID:30023290;PMID:28371479	PCS		8/9			P	HPO:probinson[2023-04-09];HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0001176	PMID:28371479	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000684	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000486	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000480	PMID:28371479	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001250	PMID:28371479	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0003155	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002066	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001252	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0003593	PMID:30023290	PCS		2/2			C	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0032794	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0410030	PMID:28371479	PCS		1/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000280	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000081	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0033725	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0009185	OMIM:280000	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:280000	CHIME syndrome		HP:0000958	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000639	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0011220	PMID:30023290;PMID:28371479	PCS		3/4			P	HPO:probinson[2023-04-09];HPO:skoehler[2012-10-17]
OMIM:280000	CHIME syndrome		HP:0012471	PMID:28371479	PCS		6/8			P	HPO:nvasilevsky[2019-03-29];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000316	PMID:30023290;PMID:28371479	PCS		8/9			P	HPO:probinson[2023-04-09];HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001249	PMID:28371479	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002553	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000175	PMID:28371479	PCS		4/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0031956	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001263	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0012385	OMIM:280000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:280000	CHIME syndrome		HP:0010281	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0008760	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0000767	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001537	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000007	PMID:22444671	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0004969	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0004209	OMIM:280000	TAS					P	HPO:probinson[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0000405	PMID:28371479	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002307	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000322	PMID:28371479	PCS		6/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000248	PMID:28371479	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000567	PMID:28371479	PCS		2/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000126	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0005338	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000687	PMID:28371479	PCS		6/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001776	PMID:28371479	PCS		2/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002562	PMID:28371479	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001156	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000023	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002240	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0031964	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0008070	PMID:28371479	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001629	PMID:28371479	PCS		2/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001507	PMID:22444671	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:280000	CHIME syndrome		HP:0001669	PMID:28371479	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0030084	PMID:30023290	PCS		2/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002557	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0000972	PMID:28371479	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000179	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0004415	PMID:28371479	PCS		1/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000396	PMID:30023290	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000154	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0002136	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0002059	PMID:28371479	PCS		5/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002213	PMID:28371479	PCS		7/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001682	PMID:28371479	PCS		1/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001520	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0000431	OMIM:280000;PMID:28371479	PCS		18/18			P	HPO:probinson[2012-05-01];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000232	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000034	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000194	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0009909	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000074	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0100040	PMID:28371479	PCS		6/7			P	HPO:nvasilevsky[2019-03-29];HPO:nvasilevsky[2019-03-29];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0005280	PMID:30023290;PMID:28371479	PCS		9/10			P	HPO:probinson[2012-05-01];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0034295	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0008064	PMID:28371479	PCS		8/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0009473	OMIM:280000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:280000	CHIME syndrome		HP:0000506	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001719	PMID:28371479	PCS		1/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000508	PMID:28371479	PCS		4/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001636	PMID:28371479	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0001833	PMID:28371479	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0002007	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0001357	OMIM:280000	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:280000	CHIME syndrome		HP:0000465	OMIM:280000	IEA					P	HPO:iea[2009-02-17]
OMIM:280000	CHIME syndrome		HP:0006721	PMID:28371479	PCS		1/8			P	HPO:probinson[2023-04-09]
OMIM:280000	CHIME syndrome		HP:0000666	PMID:30023290	PCS		1/2			P	HPO:probinson[2023-04-09]
OMIM:312210	Radiation sensitivity of natural killer activity		HP:0002715	OMIM:312210	IEA					P	HPO:iea[2009-02-17]
OMIM:312210	Radiation sensitivity of natural killer activity		HP:0001417	OMIM:312210	IEA					I	HPO:iea[2009-02-17]
OMIM:259775	Raine syndrome		HP:0002983	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0000244	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0004322	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0005257	PMID:17924334	PCS		6/7			P	HPO:probinson[2012-07-30];HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0003155	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000160	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0010808	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0003196	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000316	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000239	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000238	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0001847	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0001522	PMID:17924334	PCS		7/7			C	HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0000358	OMIM:259775	TAS		HP:0040283			P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0002553	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0000175	OMIM:259775	TAS					P	HPO:probinson[2009-02-17]
OMIM:259775	Raine syndrome		HP:0000494	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000252	OMIM:259775	TAS					P	HPO:probinson[2009-02-17]
OMIM:259775	Raine syndrome		HP:0000453	OMIM:259775	TAS					P	HPO:probinson[2012-04-29]
OMIM:259775	Raine syndrome		HP:0000695	OMIM:259775	TAS		HP:0040283			P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000452	OMIM:259775	TAS					P	HPO:probinson[2012-04-29]
OMIM:259775	Raine syndrome		HP:0001263	OMIM:259775	TAS					P	HPO:skoehler[2015-12-30]
OMIM:259775	Raine syndrome		HP:0000691	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0011800	OMIM:259775	TAS					P	HPO:skoehler[2013-11-28]
OMIM:259775	Raine syndrome		HP:0000767	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0000007	PMID:17924334	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0000520	OMIM:259775	TAS					P	HPO:probinson[2009-02-17]
OMIM:259775	Raine syndrome		HP:0000248	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0002148	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000369	OMIM:259775	TAS					P	HPO:probinson[2009-02-17]
OMIM:259775	Raine syndrome		HP:0000126	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0003577	PMID:17924334	PCS		7/7			C	HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0002089	PMID:17924334	PCS		4/7			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0001156	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:259775	Raine syndrome		HP:0031485	PMID:17924334	PCS		7/7			P	HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0011001	OMIM:259775	TAS	HP:0003623				P	HPO:probinson[2009-02-17]
OMIM:259775	Raine syndrome		HP:0011001	PMID:17924334	PCS		7/7			P	HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0006297	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0000218	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000411	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2013-05-31]
OMIM:259775	Raine syndrome		HP:0000377	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0002514	PMID:17924334	PCS		3/4			P	HPO:probinson[2012-07-30];HPO:probinson[2022-05-09]
OMIM:259775	Raine syndrome		HP:0000212	OMIM:259775	TAS					P	HPO:probinson[2012-04-29]
OMIM:259775	Raine syndrome		HP:0000410	OMIM:259775	TAS		HP:0040283			P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000154	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0000072	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:259775	Raine syndrome		HP:0000272	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0000470	OMIM:259775	TAS					P	HPO:skoehler[2012-10-17]
OMIM:259775	Raine syndrome		HP:0005280	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:259775	Raine syndrome		HP:0002804	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0006487	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0003811	OMIM:259775	IEA					C	HPO:probinson[2009-02-17]
OMIM:259775	Raine syndrome		HP:0001357	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0000303	OMIM:259775	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:259775	Raine syndrome		HP:0000347	OMIM:259775	TAS					P	HPO:probinson[2012-07-30]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0002059	PMID:22243965	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0010837	PMID:22243965	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0003676	PMID:22243965	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0001344	PMID:22243965	PCS		5/5			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0000365	PMID:22243965	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0002540	PMID:22243965	PCS		5/5			P	HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0001272	PMID:22243965	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0001250	PMID:22243965	PCS		2/5			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0001252	OMIM:614482	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0003593	PMID:22243965	PCS		5/5			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0011967	PMID:22243965	PCS		4/4			P	HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0011344	PMID:22243965	PCS		5/5			P	HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0012704	PMID:22243965	PCS		5/5			P	HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0000639	PMID:22243965	PCS		3/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0003819	PMID:22243965	PCS		5/5			C	HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0000519	PMID:22243965	PCS	HP:0003577	5/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0000007	PMID:22243965	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:614482	Congenital cataracts, hearing loss, and neurodegeneration		HP:0003429	PMID:22243965	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-07]
OMIM:257980	Odontoonychodermal dysplasia		HP:0003577	PMID:15316967	PCS		2/3			C	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0002164	PMID:15316967	PCS					P	HPO:skoehler[2013-01-22];HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0010783	OMIM:257980	TAS					P	HPO:skoehler[2013-01-22]
OMIM:257980	Odontoonychodermal dysplasia		HP:0040162	OMIM:257980	IEA					P	HPO:skoehler[2018-10-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0045075	PMID:19559398	PCS		7/10			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0011359	OMIM:257980	TAS					P	HPO:skoehler[2012-10-17]
OMIM:257980	Odontoonychodermal dysplasia		HP:0008391	OMIM:257980	TAS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0000958	PMID:19559398	PCS		6/10			P	HPO:iea[2010-04-24]
OMIM:257980	Odontoonychodermal dysplasia		HP:0010298	PMID:15316967	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0011463	PMID:15316967	PCS		1/3			C	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0001807	PMID:15316967	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0011065	PMID:15316967	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0000613	PMID:19559398	PCS		3/10			P	HPO:iea[2009-02-17]
OMIM:257980	Odontoonychodermal dysplasia		HP:0000975	PMID:19559398	PCS		2/10			P	HPO:iea[2010-04-24]
OMIM:257980	Odontoonychodermal dysplasia		HP:0000972	PMID:15316967	PCS		2/3			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0006313	PMID:15316967	PCS		3/3			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0007502	PMID:15316967	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0002213	OMIM:257980	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257980	Odontoonychodermal dysplasia		HP:0025493	PMID:15316967	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0025114	OMIM:257980	IEA					P	HPO:skoehler[2018-10-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0002231	PMID:19559398	PCS		5/8			P	HPO:iea[2010-04-24]
OMIM:257980	Odontoonychodermal dysplasia		HP:0025092	OMIM:257980	TAS					P	HPO:skoehler[2017-07-13]
OMIM:257980	Odontoonychodermal dysplasia		HP:0006481	PMID:19559398	PCS		5/11			P	HPO:iea[2009-02-17]
OMIM:257980	Odontoonychodermal dysplasia		HP:0032152	OMIM:257980	IEA					P	HPO:skoehler[2019-02-22]
OMIM:257980	Odontoonychodermal dysplasia		HP:0001816	PMID:15316967	PCS		1/3			P	HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0000668	OMIM:257980	TAS					P	HPO:skoehler[2013-01-22]
OMIM:257980	Odontoonychodermal dysplasia		HP:0002209	PMID:15316967;PMID:19559398	PCS		9/13			P	HPO:probinson[2022-05-08];HPO:iea[2009-02-17]
OMIM:257980	Odontoonychodermal dysplasia		HP:0000007	PMID:19559398	PCS					I	HPO:iea[2009-02-17]
OMIM:257980	Odontoonychodermal dysplasia		HP:0007410	PMID:15316967	PCS		1/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0000966	PMID:19559398	PCS		3/10			P	HPO:iea[2010-04-24]
OMIM:257980	Odontoonychodermal dysplasia		HP:0007556	PMID:19559398	PCS		3/10			P	HPO:iea[2009-02-17]
OMIM:257980	Odontoonychodermal dysplasia		HP:0001810	PMID:19559398	PCS		7/11			P	HPO:iea[2009-02-17]
OMIM:257980	Odontoonychodermal dysplasia		HP:0001799	PMID:15316967	PCS		3/3			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:257980	Odontoonychodermal dysplasia		HP:0006349	PMID:19559398	PCS		10/10			P	HPO:iea[2010-04-24]
OMIM:257980	Odontoonychodermal dysplasia		HP:0001798	OMIM:257980	TAS					P	HPO:skoehler[2013-01-22]
OMIM:200600	Achondrogenesis, type IA		HP:0002983	PMID:29872333	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000882	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0002089	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000463	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0001552	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0001591	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0010808	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:6000653	PMID:28744080	PCS					P	HPO:probinson[2024-05-09]
OMIM:200600	Achondrogenesis, type IA		HP:0003196	PMID:29872333	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000262	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0003175	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:6000654	PMID:23956106	PCS	HP:0034198	2/3			P	HPO:probinson[2024-05-09]
OMIM:200600	Achondrogenesis, type IA		HP:0010306	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0012368	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0010963	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0200083	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000916	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0002979	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0003826	OMIM:200600	TAS					C	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0001789	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0000774	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000894	OMIM:200600	TAS					P	HPO:probinson[2012-07-29]
OMIM:200600	Achondrogenesis, type IA		HP:0000773	PMID:29872333	PCS		1/1			P	HPO:probinson[2012-07-29];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0003521	PMID:29872333	PCS		1/1			P	HPO:probinson[2012-07-29];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0001561	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0001762	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0004331	PMID:29872333	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000470	PMID:29872333	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0010675	OMIM:200600	TAS					P	HPO:probinson[2012-07-29]
OMIM:200600	Achondrogenesis, type IA		HP:0004590	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0005281	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0005280	PMID:29872333	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0010660	OMIM:200600	TAS					P	HPO:iea[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0010880	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0034198	PMID:29872333	PCS		1/1			C	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000904	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0000007	PMID:20089971	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0006640	PMID:29872333	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0004606	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0006488	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0001538	PMID:29872333	PCS		1/1			P	HPO:probinson[2012-07-29];HPO:probinson[2022-05-18]
OMIM:200600	Achondrogenesis, type IA		HP:0006489	OMIM:200600	TAS					P	HPO:probinson[2012-07-29]
OMIM:200600	Achondrogenesis, type IA		HP:0002984	OMIM:200600	TAS					P	HPO:probinson[2009-02-17]
OMIM:200600	Achondrogenesis, type IA		HP:0000369	PMID:29872333	PCS		1/1			P	HPO:probinson[2022-05-18]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0001030	PMID:25683118	PCS		2/4			P	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0003593	PMID:25683118	PCS		4/4			C	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0025092	PMID:25683118	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0032541	PMID:25683118	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0030318	PMID:25683118	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0100792	PMID:25683118	PCS		1/1			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0000958	PMID:25683118	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0008066	PMID:25683118	PCS		4/4			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0100825	PMID:25683118	PCS		2/4			P	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0040189	PMID:25683118	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0001806	PMID:25683118	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0007530	PMID:25683118	PCS		2/4			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0000007	PMID:25683118	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0007421	PMID:25683118	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0000989	PMID:25683118	PCS		1/4			P	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0007502	PMID:25683118	PCS		1/1			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0002745	PMID:25683118	PCS		2/4			P	HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0000962	PMID:25683118	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-11]
OMIM:616295	Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads		HP:0001820	PMID:25683118	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-11]
OMIM:309630	Metacarpal 4-5 fusion		HP:0003577	PMID:23709756	PCS		2/2			C	HPO:probinson[2022-12-10]
OMIM:309630	Metacarpal 4-5 fusion		HP:0001419	PMID:23709756	PCS					I	HPO:skoehler[2013-11-18];HPO:probinson[2022-12-10]
OMIM:309630	Metacarpal 4-5 fusion		HP:0005709	PMID:23709756	PCS		1/2			P	HPO:probinson[2022-12-10]
OMIM:309630	Metacarpal 4-5 fusion		HP:0010047	PMID:23709756	PCS		2/2			P	HPO:probinson[2022-12-10]
OMIM:309630	Metacarpal 4-5 fusion		HP:0004209	PMID:23709756	PCS		1/2			P	HPO:probinson[2022-12-10]
OMIM:309630	Metacarpal 4-5 fusion		HP:0005867	PMID:23709756	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-10]
OMIM:607398	Glucocorticoid deficiency 2		HP:0000252	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0003154	PMID:27660747;PMID:16868047	PCS		2/2			P	HPO:probinson[2024-03-13];HPO:iea[2009-02-17];HPO:probinson[2022-11-26];HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0002571	PMID:27660747;PMID:16868047	PCS		1/2			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0001285	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0040084	PMID:16868047	PCS		0/1			P	HPO:probinson[2024-03-13];HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0032794	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0011344	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0012444	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0033725	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0008163	PMID:27660747;PMID:16868047	PCS		2/2			P	HPO:probinson[2024-03-13];HPO:iea[2009-02-17];HPO:probinson[2022-11-26];HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0011153	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0001988	PMID:16868047;PMID:15654338	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0000007	PMID:15654338	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-26]
OMIM:607398	Glucocorticoid deficiency 2		HP:0000953	PMID:27660747	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-26];HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0001943	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0006532	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0008689	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0003623	PMID:27660747	PCS		1/1			C	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0000522	PMID:27660747;PMID:16868047	PCS		1/2			P	HPO:probinson[2024-03-13]
OMIM:607398	Glucocorticoid deficiency 2		HP:0001336	PMID:16868047	PCS		1/1			P	HPO:probinson[2024-03-13]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003236	PMID:11381124;PMID:20106987	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003577	PMID:20729548;PMID:20106987	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0002783	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0030674	PMID:11381124	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0001252	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003273	PMID:20106987	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003593	PMID:16075202;PMID:20106987	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0001270	PMID:16075202;PMID:11506412;PMID:20729548	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0034677	PMID:20106987	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0100297	PMID:11381124;PMID:20106987	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0006094	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0100807	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0020045	PMID:11381124	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0002878	PMID:11381124	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0000218	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003701	PMID:20729548;PMID:20106987	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0001324	PMID:20106987	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003306	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0001249	PMID:11381124;PMID:11506412	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003722	PMID:11381124	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003623	PMID:11381124;PMID:11506412	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0000473	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003202	PMID:11506412;PMID:20106987	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003324	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003687	PMID:20106987	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0002650	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0031936	PMID:20106987	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0000470	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0034665	PMID:20106987	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0001181	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0008081	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0034671	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0002808	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0002827	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0001558	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0000007	PMID:11381124	PCS					I	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0030095	PMID:16075202	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003713	PMID:20106987	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0034391	PMID:16075202;PMID:11381124;PMID:11506412;PMID:20729548;PMID:20106987	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0000347	PMID:11381124	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620727	Ullrich congenital muscular dystrophy 1B		HP:0003557	PMID:16075202;PMID:11381124;PMID:20106987	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:611465	Gallbladder disease 4		HP:0001081	PMID:17632509	PCS					P	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-20]
OMIM:611465	Gallbladder disease 4		HP:0010982	PMID:17632509	PCS					I	HPO:skoehler[2013-04-01];HPO:probinson[2020-07-20]
OMIM:275300	TRACHEOBRONCHOMEGALY		HP:0006538	OMIM:275300	IEA					P	HPO:iea[2009-02-17]
OMIM:275300	TRACHEOBRONCHOMEGALY		HP:0002110	OMIM:275300	IEA					P	HPO:iea[2009-02-17]
OMIM:275300	TRACHEOBRONCHOMEGALY		HP:0006509	OMIM:275300	IEA					P	HPO:iea[2009-02-17]
OMIM:275300	TRACHEOBRONCHOMEGALY		HP:0000007	OMIM:275300	IEA					I	HPO:iea[2009-02-17]
OMIM:275300	TRACHEOBRONCHOMEGALY		HP:0001522	OMIM:275300	IEA					C	HPO:iea[2009-02-17]
OMIM:617014	Neutropenia, severe congenital, 7, autosomal recessive		HP:0033606	PMID:24753537	PCS		0/3			P	HPO:probinson[2023-04-19]
OMIM:617014	Neutropenia, severe congenital, 7, autosomal recessive		HP:0002719	PMID:24753537	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-19]
OMIM:617014	Neutropenia, severe congenital, 7, autosomal recessive		HP:0011463	PMID:24753537	PCS		1/4			C	HPO:probinson[2023-04-19]
OMIM:617014	Neutropenia, severe congenital, 7, autosomal recessive		HP:0003593	PMID:24753537	PCS		1/4			C	HPO:probinson[2023-04-19]
OMIM:617014	Neutropenia, severe congenital, 7, autosomal recessive		HP:0000007	PMID:24753537	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-19]
OMIM:617014	Neutropenia, severe congenital, 7, autosomal recessive		HP:0001875	PMID:24753537	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-19]
OMIM:617014	Neutropenia, severe congenital, 7, autosomal recessive		HP:0003623	PMID:24753537	PCS		2/4			C	HPO:probinson[2023-04-19]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0000252	PMID:11062482	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0003577	PMID:11062482	PCS		3/3			C	HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0001696	OMIM:605376	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0001651	PMID:11062482	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0003363	OMIM:605376	TAS					P	HPO:probinson[2013-03-24]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0001274	PMID:11062482	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0011599	OMIM:605376	TAS					P	HPO:probinson[2013-03-24]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0033379	PMID:11062482	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0011537	OMIM:605376	TAS					P	HPO:probinson[2013-03-24]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0001719	OMIM:605376	TAS					P	HPO:skoehler[2015-12-30]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0003829	PMID:11062482	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0001669	PMID:11062482	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0001746	PMID:11062482	PCS		1/3			P	HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0006695	OMIM:605376	TAS					P	HPO:probinson[2013-03-24]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0001748	PMID:11062482	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0000006	PMID:11062482	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-10-07]
OMIM:605376	Heterotaxy, visceral, 2, autosomal		HP:0002566	PMID:11062482	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-07]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0004322	OMIM:271600	TAS					P	HPO:probinson[2009-02-17]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0011909	OMIM:271600	TAS					P	HPO:probinson[2012-06-03]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0000926	OMIM:271600	TAS					P	HPO:probinson[2009-02-17]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0000007	OMIM:271600	TAS					I	HPO:probinson[2009-02-17]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0005194	OMIM:271600	TAS					P	HPO:probinson[2012-06-03]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0002758	OMIM:271600	TAS					P	HPO:probinson[2012-06-03]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0008843	OMIM:271600	TAS				HP:0012828	P	HPO:probinson[2012-05-27]
OMIM:271600	Spondyloepiphyseal dysplasia tarda, autosomal recessive		HP:0002655	OMIM:271600	TAS					P	HPO:probinson[2009-02-17]
DECIPHER:19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0004322	DECIPHER:19	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0000717	DECIPHER:19	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0000736	DECIPHER:19	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0000752	DECIPHER:19	IEA					P	HPO:skoehler[2013-05-29]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0001276	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0004467	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000582	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0001498	OMIM:226980	TAS					P	HPO:skoehler[2012-05-05]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0001552	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0003311	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0004322	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000083	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0002240	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0003593	PMID:10932183	PCS		5/5			C	HPO:probinson[2009-02-17];HPO:probinson[2022-10-08]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0003071	OMIM:226980	TAS					P	HPO:probinson[2013-04-08]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0010168	OMIM:226980	TAS					P	HPO:skoehler[2015-02-23]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0010585	OMIM:226980	TAS					P	HPO:probinson[2013-04-08]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0100651	OMIM:226980	TAS					P	HPO:skoehler[2015-12-30]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000939	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0010230	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0008134	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0006274	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0006110	OMIM:226980	TAS					P	HPO:probinson[2012-06-09]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0030043	OMIM:226980	TAS					P	HPO:skoehler[2015-01-20]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000316	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0003307	OMIM:226980	TAS					P	HPO:skoehler[2013-04-18]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0002857	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000218	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0002656	PMID:10932183	PCS	HP:0011463	3/3			P	HPO:probinson[2009-02-17];HPO:probinson[2022-10-08]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000831	PMID:10932183	PCS	HP:0003593	5/5			P	HPO:probinson[2015-02-23];HPO:probinson[2022-10-08]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0002654	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0003301	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0004236	OMIM:226980	TAS					P	HPO:skoehler[2012-05-05]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000252	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0002673	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0001263	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0010234	OMIM:226980	TAS					P	HPO:skoehler[2015-02-23]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0005280	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0002827	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000926	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0000007	PMID:10932183	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-10-08]
OMIM:226980	Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus		HP:0002868	OMIM:226980	TAS					P	HPO:probinson[2009-02-17]
OMIM:608652	Deafness, autosomal dominant 47		HP:0000407	PMID:12634859	PCS					P	HP:probinson[2019-03-02]
OMIM:608652	Deafness, autosomal dominant 47		HP:0000006	PMID:12634859	PCS					I	HPO:skoehler[2017-07-13];HP:probinson[2019-03-02]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0001025	OMIM:617772	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0002829	OMIM:617772	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0000509	OMIM:617772	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0011462	PMID:28847925	PCS					C	HPO:probinson[2022-10-06]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0002716	OMIM:617772	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0032323	OMIM:617772	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0001945	OMIM:617772	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0002315	OMIM:617772	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0000006	PMID:28847925	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-10-06]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0003677	PMID:28847925	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-06]
OMIM:617772	Deafness, autosomal dominant 34, with or without inflammation		HP:0001369	OMIM:617772	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001276	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000286	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001792	OMIM:601110	TAS					P	HPO:probinson[2012-03-03]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0002521	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0003577	PMID:10581255	PCS		1/1			C	HPO:probinson[2023-01-26]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000486	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001250	PMID:10581255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0002164	OMIM:601110	TAS					P	HPO:probinson[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001371	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001272	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001508	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0100807	OMIM:601110	TAS					P	HPO:probinson[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000612	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000414	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000218	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0030084	OMIM:601110	TAS					P	HPO:skoehler[2014-09-21]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001347	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000654	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001864	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0003642	PMID:10581255	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-01-26]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0002014	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0008936	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000252	PMID:10581255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0002059	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000431	OMIM:601110	TAS					P	HPO:probinson[2012-03-03]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001762	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0002013	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000193	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001285	PMID:10581255	PCS		1/1			P	HPO:probinson[2023-01-26]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001263	OMIM:601110	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001141	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0012537	OMIM:601110	TAS					P	HPO:skoehler[2014-01-28]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0001181	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0005280	OMIM:601110	TAS					P	HPO:probinson[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0009473	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0011473	OMIM:601110	TAS					P	HPO:skoehler[2013-05-29]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000007	PMID:10581255	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0002804	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000648	PMID:10581255	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-01-26]
OMIM:601110	Congenital disorder of glycosylation, type Id		HP:0000400	OMIM:601110	IEA					P	HPO:iea[2009-02-17]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0003577	PMID:25612912	PCS		2/2			C	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0004322	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0002066	PMID:25612912	PCS		2/2			P	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0002283	OMIM:300953	TAS					P	HPO:skoehler[2015-06-22]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0045055	PMID:25612912	PCS		2/2			P	HP:probinson[2019-04-19];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0045075	PMID:25612912	PCS		2/2			P	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0008070	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0041068	PMID:25612912	PCS		1/2			P	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0002719	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0001305	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0008734	PMID:25612912	PCS		2/2			P	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0006313	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0001423	PMID:25612912	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0002217	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0005328	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000556	PMID:25612912	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000253	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000154	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0002136	PMID:25612912	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000252	OMIM:300953	TAS					P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000054	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000992	OMIM:300953	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000750	PMID:25612912	PCS		2/2			P	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000871	PMID:25612912	PCS		1/2			P	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0002299	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0001321	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0034425	PMID:25612912	PCS		2/2			P	HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000609	PMID:25612912	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000965	OMIM:300953	TAS					P	HPO:skoehler[2015-06-22]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000348	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0001511	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0000303	PMID:25612912	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2023-01-20]
OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		HP:0002028	OMIM:300953	TAS					P	HPO:skoehler[2015-12-30]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000286	PMID:25966638	PCS		3/9			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0003577	PMID:25966638	PCS					C	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0003016	PMID:25966638	PCS		8/8			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0002265	PMID:25966638	PCS		5/8			P	HPO:iea[2009-02-17];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0002089	PMID:25966638	PCS		9/9			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0002101	PMID:25966638	PCS		4/4			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0001371	PMID:25966638	PCS		1/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000260	PMID:25966638	PCS		4/6			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0003375	PMID:25966638	PCS		8/8			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0032313	PMID:25966638	PCS					P	HP:probinson[2019-04-19]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000319	PMID:25966638	PCS		10/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0009487	PMID:25966638	PCS		8/8			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000316	PMID:25966638	PCS		6/9			P	HPO:iea[2009-02-17];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0001405	PMID:25966638	PCS		6/8			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0001627	PMID:25966638	PCS	HP:0003577	6/8			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000813	PMID:25966638	PCS		3/3	FEMALE		P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000113	PMID:25966638	PCS		9/10			P	HPO:iea[2009-02-17];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000278	PMID:25966638	PCS		9/9			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000776	PMID:25966638	PCS		1/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000358	PMID:25966638	PCS		10/10			P	HPO:iea[2009-02-17];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0001562	PMID:25966638	PCS		1/5			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0003026	PMID:25966638	PCS		10/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0002652	OMIM:263210	TAS					P	HPO:skoehler[2017-07-13]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000252	PMID:25966638	PCS		9/11			P	HPO:probinson[2012-05-01];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0001561	PMID:25966638	PCS		1/5			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000474	PMID:25966638	PCS		9/9			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000430	PMID:25966638;OMIM:263210	PCS		19/19			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0004331	PMID:25966638	PCS		7/8			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000470	PMID:25966638	PCS		9/9			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000506	PMID:25966638	PCS		6/9			P	HPO:iea[2009-02-17];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000007	PMID:25966638	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0001539	PMID:25966638	PCS		2/5			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000444	PMID:25966638;OMIM:263210	PCS		20/20			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000520	PMID:25966638	PCS		8/9			P	HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000248	OMIM:263210	TAS					P	HPO:probinson[2012-05-01]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000369	PMID:25966638	PCS		10/10			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:263210	Gillessen-Kaesbach-Nishimura syndrome		HP:0000347	PMID:25966638	PCS		9/9			P	HPO:skoehler[2017-07-13];HP:probinson[2019-02-02]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002300	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002067	PMID:12325083	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002063	PMID:12325083	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002141	PMID:12325083	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002185	PMID:12325083	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0100256	PMID:12325083	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000737	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0031908	PMID:12325083	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0200147	OMIM:601104	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000613	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000658	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002439	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002059	PMID:12325083	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002015	PMID:12325083	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000651	OMIM:601104	PCS					P	HPO:probinson[2012-04-06]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0001300	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002530	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002354	OMIM:601104	PCS					P	HPO:probinson[2012-03-18]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0001260	PMID:12325083	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0003584	PMID:12325083	PCS		1/1			C	HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002451	OMIM:601104	PCS					P	HPO:probinson[2012-03-18];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0003581	OMIM:601104	PCS					C	HPO:probinson[2012-03-18]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002171	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002172	PMID:12325083	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000605	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002528	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002529	OMIM:601104	PCS					P	HPO:probinson[2012-03-18]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002527	PMID:12325083	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002304	OMIM:601104	PCS					P	HPO:probinson[2012-03-18]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000741	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000006	OMIM:601104	IEA					I	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000622	OMIM:601104	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0000743	OMIM:601104	PCS					P	HPO:probinson[2012-03-18];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002544	OMIM:601104	IEA					P	HPO:iea[2009-02-17]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0001337	OMIM:601104	PCS					P	HPO:probinson[2012-03-18];HPO:probinson[2022-09-03]
OMIM:601104	Supranuclear palsy, progressive, 1		HP:0002446	PMID:12325083	PCS		1/1			P	HPO:probinson[2022-09-03]
OMIM:135950	Finger locking, recurrent, with intrauterine growth retardation andproportionate short stature		HP:0004322	OMIM:135950	IEA					P	HPO:iea[2009-02-17]
OMIM:135950	Finger locking, recurrent, with intrauterine growth retardation andproportionate short stature		HP:0001511	OMIM:135950	TAS					P	HPO:probinson[2013-02-25]
OMIM:135950	Finger locking, recurrent, with intrauterine growth retardation andproportionate short stature		HP:0000006	OMIM:135950	IEA					I	HPO:iea[2009-02-17]
OMIM:605362	Cardiomyopathy, dilated, 1J		HP:0000407	PMID:10769282	IEA	HP:0003621				P	HPO:probinson[2013-02-23]
OMIM:605362	Cardiomyopathy, dilated, 1J		HP:0001635	PMID:10769282	IEA					P	HPO:probinson[2013-02-23]
OMIM:605362	Cardiomyopathy, dilated, 1J		HP:0005162	OMIM:605362	IEA					P	HPO:skoehler[2019-02-22]
OMIM:605362	Cardiomyopathy, dilated, 1J		HP:0000006	PMID:10769282	IEA					I	HPO:probinson[2013-01-09]
OMIM:605362	Cardiomyopathy, dilated, 1J		HP:0001645	PMID:10769282	IEA					P	HPO:probinson[2013-02-23]
OMIM:605362	Cardiomyopathy, dilated, 1J		HP:0001644	PMID:10769282	IEA	HP:0003581				P	HPO:probinson[2013-02-23]
OMIM:605362	Cardiomyopathy, dilated, 1J		HP:0001699	OMIM:605362	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0001287	OMIM:613500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0002850	PMID:9419212	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0004432	PMID:9419212	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0002718	PMID:25502423	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0003593	PMID:9419212	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0030252	PMID:9419212	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0000007	PMID:9419212	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0000403	PMID:9419212	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0006532	OMIM:613500	TAS					P	HPO:skoehler[2012-11-21]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0002205	OMIM:613500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0002843	PMID:9419212	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-03-26]
OMIM:613500	Agammaglobulinemia 2, autosomal recessive		HP:0002720	PMID:9419212	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0001100	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0002211	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0001053	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0002251	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0000407	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0000635	OMIM:613266	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0000458	OMIM:613266	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0002216	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0002227	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0007732	OMIM:613266	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0000135	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0000006	PMID:9462749	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-03]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0000028	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613266	Waardenburg syndrome, type 4C		HP:0002226	OMIM:613266	IEA					P	HPO:skoehler[2010-06-19]
OMIM:190320	Trichodentoosseous syndrome		HP:0001595	OMIM:190320	IEA					P	HPO:iea[2009-02-17]
OMIM:190320	Trichodentoosseous syndrome		HP:0000264	OMIM:190320	TAS					P	HPO:iea[2015-03-22]
OMIM:190320	Trichodentoosseous syndrome		HP:0001808	OMIM:190320	IEA					P	HPO:iea[2009-02-17]
OMIM:190320	Trichodentoosseous syndrome		HP:0011001	OMIM:190320	TAS					P	HPO:iea[2009-02-17]
OMIM:190320	Trichodentoosseous syndrome		HP:0000691	OMIM:190320	TAS					P	HPO:probinson[2013-04-09]
OMIM:190320	Trichodentoosseous syndrome		HP:0000679	OMIM:190320	TAS					P	HPO:iea[2009-02-17]
OMIM:190320	Trichodentoosseous syndrome		HP:0000268	OMIM:190320	TAS					P	HPO:iea[2009-02-17]
OMIM:190320	Trichodentoosseous syndrome		HP:0002007	OMIM:190320	TAS					P	HPO:iea[2009-02-17]
OMIM:190320	Trichodentoosseous syndrome		HP:0000006	OMIM:190320	TAS					I	HPO:iea[2009-02-17]
OMIM:190320	Trichodentoosseous syndrome		HP:0000687	OMIM:190320	TAS					P	HPO:probinson[2013-04-09]
OMIM:603075	Macular degeneration, age-related, 1		HP:0030499	PMID:15013873	PCS	HP:0003584				P	HP:probinson[2018-07-08]
OMIM:603075	Macular degeneration, age-related, 1		HP:0030499	PMID:9715689	PCS		10/10			P	HPO:probinson[2021-07-05]
OMIM:603075	Macular degeneration, age-related, 1		HP:0011506	OMIM:603075	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:603075	Macular degeneration, age-related, 1		HP:0000529	PMID:15013873	PCS	HP:0003584				P	HPO:skoehler[2015-12-30]
OMIM:603075	Macular degeneration, age-related, 1		HP:0003584	PMID:9715689	PCS		7/7			C	HPO:probinson[2021-07-05]
OMIM:603075	Macular degeneration, age-related, 1		HP:0031609	PMID:15013873	PCS	HP:0003584				P	HP:probinson[2018-07-08]
OMIM:603075	Macular degeneration, age-related, 1		HP:0031609	PMID:9715689	PCS		5/10			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:603075	Macular degeneration, age-related, 1		HP:0000608	PMID:15013873;PMID:9715689	PCS		18/20			P	HP:probinson[2018-07-08];HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:603075	Macular degeneration, age-related, 1		HP:0025574	OMIM:603075	TAS		HP:0040283			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-03]
OMIM:603075	Macular degeneration, age-related, 1		HP:0012643	OMIM:603075	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603075	Macular degeneration, age-related, 1		HP:0000006	PMID:9715689	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-05]
OMIM:615617	Immunodeficiency 19		HP:0012176	PMID:14602880	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-05]
OMIM:615617	Immunodeficiency 19		HP:0005403	PMID:14602880	PCS		3/3			P	HPO:probinson[2023-02-05]
OMIM:615617	Immunodeficiency 19		HP:0001508	OMIM:615617	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615617	Immunodeficiency 19		HP:0031691	PMID:14602880	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:615617	Immunodeficiency 19		HP:0004430	PMID:14602880	PCS		3/3			P	HPO:probinson[2023-02-05]
OMIM:615617	Immunodeficiency 19		HP:0003593	PMID:14602880	PCS		2/2			C	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-05]
OMIM:615617	Immunodeficiency 19		HP:0000007	PMID:14602880	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-05]
OMIM:615617	Immunodeficiency 19		HP:0000403	OMIM:615617	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615617	Immunodeficiency 19		HP:0002846	PMID:14602880	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-05]
OMIM:615617	Immunodeficiency 19		HP:0002205	OMIM:615617	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615617	Immunodeficiency 19		HP:0002028	PMID:14602880	PCS		1/3			P	HPO:probinson[2023-02-05]
OMIM:221745	Deafness, sensorineural, Autosomal-Mitochondrial type		HP:0003621	OMIM:221745	IEA					C	HPO:iea[2009-02-17]
OMIM:221745	Deafness, sensorineural, Autosomal-Mitochondrial type		HP:0000408	OMIM:221745	TAS					P	HPO:skoehler[2012-10-17]
OMIM:221745	Deafness, sensorineural, Autosomal-Mitochondrial type		HP:0000407	OMIM:221745	IEA					P	HPO:skoehler[2010-06-20]
OMIM:221745	Deafness, sensorineural, Autosomal-Mitochondrial type		HP:0001427	OMIM:221745	TAS					I	HPO:skoehler[2012-10-17]
OMIM:221745	Deafness, sensorineural, Autosomal-Mitochondrial type		HP:0000007	OMIM:221745	IEA					I	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0025100	PMID:29300384	PCS		77.8%			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0000684	OMIM:235730;PMID:29300384	PCS		15/20			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0004961	PMID:17958891;PMID:29300384	PCS		14/433			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000486	PMID:29300384	PCS		56.8%			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0004322	PMID:17958891;PMID:29300384	PCS		104/224			P	HPO:iea[2018-03-12];HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0001250	PMID:17958891;PMID:29300384	PCS		343/446			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0002021	PMID:29300384	PCS		14/190			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0001252	PMID:12920073	PCS		7/22			P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000482	OMIM:235730	IEA					P	HPO:skoehler[2019-09-07]
OMIM:235730	Mowat-Wilson syndrome		HP:0004362	PMID:17958891	PCS					P	HPO:iea[2018-03-13]
OMIM:235730	Mowat-Wilson syndrome		HP:0001290	OMIM:235730	TAS					P	HPO:skoehler[2017-07-13]
OMIM:235730	Mowat-Wilson syndrome		HP:0001290	PMID:29300384	PCS	HP:0003593	79.1%			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0003270	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0012429	PMID:29300384	PCS		40.7%			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0000518	OMIM:235730	IEA					P	HPO:skoehler[2019-09-07]
OMIM:235730	Mowat-Wilson syndrome		HP:0000316	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0007048	OMIM:235730	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:235730	Mowat-Wilson syndrome		HP:0001643	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0002019	PMID:17958891;PMID:29300384	PCS		109/383			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0001642	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0009748	OMIM:235730	IEA					P	HPO:iea[2009-12-18]
OMIM:235730	Mowat-Wilson syndrome		HP:0000176	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000494	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0003720	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000252	PMID:17958891;PMID:29300384	PCS		379/480			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000692	OMIM:235730;PMID:29300384	PCS		20/20			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000175	PMID:17958891;PMID:29300384	PCS		9/395			P	HPO:iea[2018-03-13];HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0001344	OMIM:235730;PMID:29300384	PCS		68/96			P	HPO:skoehler[2013-01-22];HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0002079	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000490	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000767	OMIM:235730	TAS					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000403	PMID:29300384	PCS		34.6%			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0000568	OMIM:235730	IEA					P	HPO:skoehler[2019-09-07]
OMIM:235730	Mowat-Wilson syndrome		HP:0002307	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000768	OMIM:235730	TAS					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000048	PMID:17958891	IEA		3/63			P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000565	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000047	PMID:12920073	PCS		3/22	MALE		P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000047	PMID:29300384	PCS		71/119			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0000006	PMID:17958891	PCS					I	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000567	OMIM:235730	IEA					P	HPO:skoehler[2019-09-07]
OMIM:235730	Mowat-Wilson syndrome		HP:0000687	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0009918	OMIM:235730	IEA					P	HPO:skoehler[2019-09-07]
OMIM:235730	Mowat-Wilson syndrome		HP:0001274	PMID:12920073	PCS		5/22			P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0001273	PMID:29300384	PCS		79.6%			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0005274	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0001270	PMID:12920073	PCS					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0040082	OMIM:235730	TAS					P	HPO:skoehler[2014-11-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0001629	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0012372	PMID:29300384	PCS		22/221			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0000612	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0001627	PMID:29300384	PCS		193/332			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0002119	OMIM:235730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:235730	Mowat-Wilson syndrome		HP:0009765	PMID:17103451	PCS		3/3			P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000378	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0002558	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0004415	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000077	PMID:29300384	PCS		59/233			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0000750	PMID:17103451	PCS		100%			P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000431	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0002013	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000078	PMID:29300384	PCS		105/244			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:235730	Mowat-Wilson syndrome		HP:0002251	PMID:26156877;PMID:29300384;PMID:12920073	PCS		272/613			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27];HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0009909	PMID:17958891	PCS					P	HPO:iea[2009-12-18]
OMIM:235730	Mowat-Wilson syndrome		HP:0011229	OMIM:235730	TAS					P	HPO:skoehler[2013-01-22]
OMIM:235730	Mowat-Wilson syndrome		HP:0000508	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000307	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0001631	OMIM:235730	IEA					P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000028	PMID:17958891	IEA		23/63	MALE		P	HPO:iea[2009-02-17]
OMIM:235730	Mowat-Wilson syndrome		HP:0000028	PMID:29300384	PCS		51/123			P	HPO:lccarmody[2018-09-27];HPO:lccarmody[2018-09-27]
OMIM:146000	Hypochondroplasia		HP:0003015	OMIM:146000	TAS				HP:0012825	P	HPO:probinson[2012-05-05]
OMIM:146000	Hypochondroplasia		HP:0003026	PMID:10777366	PCS		2/2		HP:0012825	P	HPO:probinson[2012-05-05];HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0009815	OMIM:146000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:146000	Hypochondroplasia		HP:0001363	PMID:10777366	PCS		0/2			P	HPO:probinson[2012-07-24];HPO:probinson[2024-03-08]
OMIM:146000	Hypochondroplasia		HP:0003621	PMID:10777366	PCS		1/1			C	HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0001377	OMIM:146000	IEA					P	HPO:iea[2009-02-17]
OMIM:146000	Hypochondroplasia		HP:0001156	OMIM:146000	IEA					P	HPO:iea[2009-02-17]
OMIM:146000	Hypochondroplasia		HP:0002970	OMIM:146000	IEA					P	HPO:iea[2009-02-17]
OMIM:146000	Hypochondroplasia		HP:0000272	OMIM:146000	IEA					P	HPO:iea[2009-02-17]
OMIM:146000	Hypochondroplasia		HP:0012679	PMID:10777366	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0004060	PMID:10777366	PCS		0/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0005280	PMID:10777366	PCS		2/2			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0100864	PMID:10777366	PCS		1/2			P	HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0011220	PMID:10777366	PCS		2/2			P	HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0002938	PMID:10777366	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0008873	PMID:10777366	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0000956	OMIM:146000	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:146000	Hypochondroplasia		HP:0002007	OMIM:146000	IEA					P	HPO:iea[2009-02-17]
OMIM:146000	Hypochondroplasia		HP:0000256	PMID:10777366	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0000006	PMID:7670477	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:146000	Hypochondroplasia		HP:0001249	OMIM:146000	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000286	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000582	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000321	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000486	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000387	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000365	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0002002	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000581	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0012745	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0010621	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0012368	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0011220	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0012450	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0001845	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000219	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0001249	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000750	PMID:29460469	PCS		1/1			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0031936	PMID:29460469	PCS		1/1			P	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000293	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0001382	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0005280	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000729	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0001852	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0002788	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000006	PMID:29460469	PCS					I	HPO:probinson[2020-07-25];HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000446	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0000347	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0002588	PMID:29460469	PCS		1/2			P	HPO:probinson[2020-07-25]
OMIM:618333	Menke-Hennekam syndrome 2		HP:0006349	PMID:29460469	PCS		2/2			P	HPO:probinson[2020-07-25]
OMIM:614521	Thrombocythemia 3		HP:0001894	PMID:22397670	PCS		6/6			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-26]
OMIM:614521	Thrombocythemia 3		HP:0001442	OMIM:614521	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614521	Thrombocythemia 3		HP:0002140	PMID:22397670	PCS	HP:0003581	2/6			P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:614521	Thrombocythemia 3		HP:0031386	PMID:22397670	IEA					P	HPO:probinson[2022-03-27];HPO:probinson[2022-03-27]
OMIM:614521	Thrombocythemia 3		HP:0000006	PMID:22397670	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0004325	PMID:32761064	PCS		2/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002188	PMID:32761064	PCS		2/6			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0001250	PMID:32761064	PCS		6/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0003196	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0012745	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0012427	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0010763	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0031861	PMID:32761064	PCS		1/3			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0011343	PMID:32761064	PCS		2/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0012471	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000678	PMID:32761064	PCS		2/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0001249	PMID:32761064	PCS					P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0007328	PMID:32761064	PCS		2/8			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002553	PMID:32761064	PCS		2/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000054	PMID:32761064	PCS		2/7	MALE		P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002353	PMID:32761064	PCS		6/7			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000729	PMID:32761064	PCS		1/5			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000007	PMID:32761064	PCS					I	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000527	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000522	PMID:32761064	PCS		1/8			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002028	PMID:32761064	PCS		1/7			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000463	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002240	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0001270	PMID:32761064	PCS		7/8			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0012450	PMID:32761064	PCS		3/7			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000337	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000733	PMID:32761064	PCS		1/5			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000218	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000577	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000750	PMID:32761064	PCS		7/8			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0020062	PMID:32761064	PCS		3/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002650	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000430	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0011344	PMID:32761064	PCS		5/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0012510	PMID:32761064	PCS		1/6			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0005280	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0003819	PMID:32761064	PCS		1/9			C	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002808	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000348	PMID:32761064	PCS		2/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0001319	PMID:32761064	PCS	HP:0003623	3/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000307	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0001511	PMID:32761064	PCS	HP:0003577	1/8			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002007	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0001357	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000268	PMID:32761064	PCS		2/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0001873	PMID:32761064	PCS		1/8			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0007018	PMID:32761064	PCS		2/5			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0002643	PMID:32761064	PCS	HP:0003623	3/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000028	PMID:32761064	PCS		3/7	MALE		P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000347	PMID:32761064	PCS		1/9			P	HPO:probinson[2020-12-03]
OMIM:619005	Neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia		HP:0000742	PMID:32761064	PCS		1/8			P	HPO:probinson[2020-12-03]
OMIM:617028	Intellectual developmental disorder, autosomal recessive 54		HP:0002267	PMID:27106596	PCS		1/4			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:617028	Intellectual developmental disorder, autosomal recessive 54		HP:0000750	PMID:27106596	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:617028	Intellectual developmental disorder, autosomal recessive 54		HP:0003593	PMID:27106596	PCS		4/4			C	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:617028	Intellectual developmental disorder, autosomal recessive 54		HP:0000712	PMID:27106596	PCS		1/4			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:617028	Intellectual developmental disorder, autosomal recessive 54		HP:0000007	PMID:27106596	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:617028	Intellectual developmental disorder, autosomal recessive 54		HP:0007018	PMID:27106596	PCS		1/4			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:617028	Intellectual developmental disorder, autosomal recessive 54		HP:0001249	PMID:27106596	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-26]
OMIM:610021	Hyperinsulinemic hypoglycemia, familial, 7		HP:0004510	PMID:1358043	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-04]
OMIM:610021	Hyperinsulinemic hypoglycemia, familial, 7		HP:0000825	PMID:17701893	PCS				HP:0025377	P	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-04]
OMIM:610021	Hyperinsulinemic hypoglycemia, familial, 7		HP:0002173	PMID:11207177	PCS				HP:0025377	P	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-04]
OMIM:610021	Hyperinsulinemic hypoglycemia, familial, 7		HP:0001943	PMID:17701893	PCS				HP:0025377	P	HPO:probinson[2013-12-15];HPO:probinson[2020-09-04]
OMIM:610021	Hyperinsulinemic hypoglycemia, familial, 7		HP:0000006	PMID:17701893	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2020-09-04]
OMIM:610021	Hyperinsulinemic hypoglycemia, familial, 7		HP:0000842	PMID:17701893	PCS				HP:0025377	P	HPO:probinson[2009-02-17];HPO:probinson[2020-09-04]
OMIM:617996	Oocyte maturation defect 5		HP:0034719	PMID:29606300	PCS		4/4			P	HPO:probinson[2023-06-05]
OMIM:617996	Oocyte maturation defect 5		HP:0008222	PMID:29606300	PCS		4/4			P	HPO:probinson[2023-02-17]
OMIM:617996	Oocyte maturation defect 5		HP:0011462	PMID:29606300	PCS		4/4			C	HPO:probinson[2023-02-17]
OMIM:617996	Oocyte maturation defect 5		HP:0000007	PMID:29606300	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0008936	PMID:18439546	PCS		20/20			P	HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0001344	PMID:18439546	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0002540	PMID:18439546	PCS		20/20			P	HPO:skoehler[2018-10-08]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0003200	PMID:18439546	PCS		0/3			P	HPO:probinson[2023-05-17];HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0001332	PMID:18439546	PCS		20/20			P	HPO:skoehler[2013-10-06]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0011924	PMID:18439546	PCS		3/3			P	HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0001263	PMID:18439546	PCS		20/20			P	HPO:skoehler[2013-10-06]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0002151	PMID:18439546	PCS		20/20			P	HPO:skoehler[2013-10-06]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0001251	PMID:18439546	PCS		20/20			P	HPO:skoehler[2013-10-06]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0003593	PMID:18439546	PCS					C	HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0002071	PMID:18439546	PCS		20/20			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0000007	PMID:18439546	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0000711	PMID:18439546	PCS		20/20			P	HPO:probinson[2023-05-17]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0002305	PMID:18439546	PCS		20/20			P	HPO:skoehler[2013-10-06]
OMIM:615159	Mitochondrial complex III deficiency, nuclear type 4		HP:0001347	PMID:18439546	PCS		20/20			P	HPO:skoehler[2013-10-06]
OMIM:115470	Cat eye syndrome		HP:0002025	PMID:11693792	PCS		6/88			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0025023	PMID:11693792	PCS		3/88			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0002245	PMID:11693792	PCS		2/48			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000286	PMID:11693792	PCS		29/45			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0004467	OMIM:115470	IEA					P	HPO:iea[2009-02-17]
OMIM:115470	Cat eye syndrome		HP:0000384	OMIM:115470	IEA					P	HPO:iea[2009-02-17]
OMIM:115470	Cat eye syndrome		HP:0003577	PMID:11693792	PCS					C	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0002023	PMID:11693792	PCS		61/88			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000365	PMID:11693792	PCS		11/68			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0004322	PMID:11693792	PCS		32/64			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0002580	PMID:11693792	PCS		2/48			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000085	PMID:11693792	PCS		2/77			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0004383	PMID:11693792	PCS		2/80			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0100590	PMID:11693792	PCS		36/88			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0001629	PMID:11693792	PCS		18/80			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0011662	PMID:11693792	PCS		3/80			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0001507	OMIM:115470	IEA					P	HPO:iea[2009-02-17]
OMIM:115470	Cat eye syndrome		HP:0000316	PMID:11693792	PCS		48/69			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000612	OMIM:115470	TAS					P	HPO:probinson[2009-02-17]
OMIM:115470	Cat eye syndrome		HP:0001643	PMID:11693792	PCS		7/80			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0001642	PMID:11693792	PCS		5/80			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000175	PMID:11693792	PCS		15/48			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000494	PMID:11693792	PCS		48/70			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000076	PMID:11693792	PCS		13/77			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0005160	PMID:11693792	PCS		15/80			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0001636	PMID:11693792	PCS		7/80			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0001537	PMID:11693792	PCS		8/48			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000568	PMID:11693792	PCS		23/59			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0005912	PMID:11693792	PCS		4/48			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0001631	PMID:11693792	PCS		15/80			P	HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0003974	OMIM:115470	IEA					P	HPO:iea[2009-02-17]
OMIM:115470	Cat eye syndrome		HP:0000006	PMID:11693792	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000567	PMID:11693792	PCS		54/88			P	HPO:probinson[2015-07-19];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0002566	PMID:11693792	PCS		8/48			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000369	PMID:11693792	PCS		42/61			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000347	PMID:11693792	PCS		27/48			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000402	OMIM:115470	IEA					P	HPO:iea[2009-02-17]
OMIM:115470	Cat eye syndrome		HP:0000104	PMID:11693792	PCS		18/77			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-25]
OMIM:115470	Cat eye syndrome		HP:0000126	PMID:11693792	PCS		13/77			P	HPO:probinson[2022-09-25]
DECIPHER:31	Hereditary Liability to Pressure Palsies (HNPP)		HP:0012078	DECIPHER:31	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:31	Hereditary Liability to Pressure Palsies (HNPP)		HP:0002450	DECIPHER:31	IEA					P	HPO:skoehler[2013-05-29]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0000175	PMID:29805041	PCS		1/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0030039	PMID:29805041	PCS		10/10			P	HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0006109	PMID:29805041	PCS		6/9			P	HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0001762	PMID:29805041	PCS		1/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0002650	PMID:29805041	PCS		10/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0001371	PMID:29805041	PCS		10/10			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0009760	PMID:29805041	PCS		2/9			P	HPO:probinson[2019-11-28];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0000470	PMID:29805041	PCS		6/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0002949	PMID:29805041	PCS		4/10			P	HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0000007	PMID:29805041	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0008368	PMID:29805041	PCS		6/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:618469	Contractures, pterygia, and variable skeletal fusions syndrome 1B		HP:0000465	PMID:29805041	PCS		5/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-11-28]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002069	PMID:33280099	PCS		3/9			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0010804	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000486	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002188	PMID:33280099	PCS		2/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001250	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002066	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0010808	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001252	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002020	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0012708	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0012745	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0032794	PMID:30160831;PMID:33280099	PCS		2/10			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0012389	PMID:33280099	PCS		3/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0033725	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0012469	PMID:33280099	PCS		3/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001804	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000954	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001249	PMID:33280099	PCS		9/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001265	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002870	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001266	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000691	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001263	PMID:30160831;PMID:33280099	PCS		10/10			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002072	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0100660	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0005619	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0005617	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002307	PMID:33280099	PCS		4/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000565	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002987	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0007359	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000006	PMID:30160831	PCS					I	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001336	PMID:30160831;PMID:33280099	PCS		4/10			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001156	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0031045	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002280	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0012444	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0006297	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0012450	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000733	PMID:33280099	PCS		2/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002119	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002835	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000218	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000455	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001302	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000212	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001028	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0008936	PMID:33280099	PCS		5/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002015	PMID:30160831;PMID:33280099	PCS		4/10			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002059	PMID:33280099	PCS		3/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002650	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002376	PMID:33280099	PCS		5/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002373	PMID:33280099	PCS		2/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001284	PMID:30160831;PMID:33280099	PCS		3/10			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0010852	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0011147	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0010536	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0005280	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0032667	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0032792	PMID:33280099	PCS		4/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0001558	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000549	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000664	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0200055	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002205	PMID:33280099	PCS		2/9			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0000347	PMID:30160831	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619777	Developmental and epileptic encephalopathy 100		HP:0002126	PMID:33280099	PCS		1/9			P	HPO:probinson[2022-05-29]
OMIM:617982	Ververi-Brady syndrome		HP:0000582	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0003577	PMID:30281152	PCS		2/2			C	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0004322	PMID:30281152	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0001195	PMID:30281152	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0001252	PMID:30281152;PMID:28692176	PCS		2/5			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0001270	PMID:30281152;PMID:28692176	PCS		4/5			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0002080	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000319	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000316	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0001669	PMID:30281152	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000414	PMID:30281152	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000219	PMID:30281152;PMID:28692176	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0002317	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000218	PMID:30281152	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000455	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000378	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0001249	PMID:28692176	PCS		3/3			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0001265	PMID:28692176	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000154	PMID:30281152;PMID:28692176	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000252	PMID:28692176	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000750	PMID:30281152;PMID:28692176	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0002650	PMID:30281152	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000232	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0002750	PMID:30281152	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0003025	PMID:30281152	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0011968	PMID:30281152	PCS		1/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0008180	PMID:28692176	PCS	HP:0011463	2/3			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000729	PMID:28692176	PCS		1/3			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000508	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000448	PMID:28692176	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0004209	PMID:30281152	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0001511	PMID:28692176	PCS		0/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000400	PMID:30281152	PCS		2/2			P	HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000006	PMID:28692176	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000369	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:617982	Ververi-Brady syndrome		HP:0000445	PMID:28692176	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-06-27]
OMIM:620848	Spermatogenic failure 92		HP:0034011	PMID:37804054;PMID:38091523	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0032560	PMID:37804054	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0003251	PMID:37804054;PMID:38091523	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0011462	PMID:37804054;PMID:38091523	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0012207	PMID:37804054;PMID:38091523	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0000007	PMID:37804054	PCS					I	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0034811	PMID:37804054	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0000798	PMID:37804054;PMID:38091523	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0032558	PMID:37804054	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620848	Spermatogenic failure 92		HP:0032559	PMID:37804054	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:619011	Oocyte maturation defect 9		HP:0008222	PMID:32473092	PCS		5/5			P	HPO:probinson[2020-11-29]
OMIM:619011	Oocyte maturation defect 9		HP:0011462	PMID:32473092	PCS		5/5			C	HPO:probinson[2024-03-16]
OMIM:619011	Oocyte maturation defect 9		HP:0000140	PMID:32473092	PCS		0/5			P	HPO:probinson[2020-11-29];HPO:probinson[2024-03-16]
OMIM:619011	Oocyte maturation defect 9		HP:0000007	PMID:32473092	PCS					I	HPO:probinson[2020-11-29];HPO:probinson[2020-11-29]
OMIM:619011	Oocyte maturation defect 9		HP:0033336	PMID:32473092	PCS		1/4			P	HPO:probinson[2020-12-07]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0010628	OMIM:616322	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0003388	PMID:11435464	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0011968	PMID:11435464	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0003473	PMID:11435464	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0001252	PMID:11435464	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0003593	OMIM:616322	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0002093	PMID:11435464	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0000508	PMID:11435464	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0000602	PMID:11435464	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0000007	PMID:11435464	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0001558	OMIM:616322	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0001319	OMIM:616322	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0000218	OMIM:616322	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0001324	OMIM:616322	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0001612	PMID:11435464	PCS		1/1			P	HPO:probinson[2023-02-26]
OMIM:616322	Myasthenic syndrome, congenital, 3B, fast-channel		HP:0000467	OMIM:616322	TAS					P	HPO:skoehler[2015-05-31]
OMIM:620690	Developmental dysplasia of the hip 3		HP:0001374	PMID:36067312	PCS					P	HPO:probinson[2024-04-06]
OMIM:620690	Developmental dysplasia of the hip 3		HP:0003274	PMID:36067312	PCS					P	HPO:probinson[2024-04-06]
OMIM:620690	Developmental dysplasia of the hip 3		HP:0003593	PMID:36067312	PCS					C	HPO:probinson[2024-04-06]
OMIM:620690	Developmental dysplasia of the hip 3		HP:0000006	PMID:36067312	PCS					I	HPO:probinson[2024-04-06]
OMIM:610753	Alopecia areata 2		HP:0002289	PMID:17236136	PCS					P	HPO:skoehler[2017-07-13]
OMIM:610753	Alopecia areata 2		HP:0007418	PMID:17236136	PCS					P	HPO:lccarmody[2018-06-13]
OMIM:610753	Alopecia areata 2		HP:0002232	PMID:17236136	PCS					P	HPO:lccarmody[2018-06-13]
OMIM:610753	Alopecia areata 2		HP:0003829	PMID:17236136	PCS					I	HPO:skoehler[2017-07-13]
OMIM:610753	Alopecia areata 2		HP:0001426	PMID:17236136	PCS					I	HPO:lccarmody[2018-06-13]
OMIM:610753	Alopecia areata 2		HP:0002293	PMID:17236136	PCS					P	HPO:lccarmody[2018-06-13]
OMIM:610753	Alopecia areata 2		HP:0000007	OMIM:610753	IEA					I	HPO:skoehler[2018-10-08]
OMIM:610753	Alopecia areata 2		HP:0000006	OMIM:610753	IEA					I	HPO:skoehler[2018-10-08]
OMIM:208300	Ascites, chylous		HP:0000007	OMIM:208300	IEA					I	HPO:iea[2009-02-17]
OMIM:208300	Ascites, chylous		HP:0012281	OMIM:208300	TAS	HP:0003577				P	HPO:probinson[2013-04-07]
OMIM:208300	Ascites, chylous		HP:0000501	OMIM:208300	TAS					P	HPO:skoehler[2010-06-20]
OMIM:245200	Krabbe disease		HP:0006801	OMIM:245200	PCS					P	HPO:probinson[2012-04-11]
OMIM:245200	Krabbe disease		HP:0001276	PMID:20886637	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0000365	OMIM:245200	PCS					P	HPO:probinson[2012-04-11]
OMIM:245200	Krabbe disease		HP:0001250	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0001252	PMID:20886637	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0003593	PMID:20886637	PCS		25/30			C	HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0002180	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0001508	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0000639	PMID:20886637	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0007141	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0011463	PMID:20886637	PCS		4/30			C	HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0011462	PMID:20886637	PCS		1/30			C	HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0034322	PMID:20886637	PCS		29/29			P	HPO:probinson[2022-09-05];HPO:probinson[2024-08-04]
OMIM:245200	Krabbe disease		HP:0000618	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0000238	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0007305	PMID:20886637	PCS		5/22			P	HPO:probinson[2012-04-11];HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0002333	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0008936	PMID:20886637	PCS		23/30			P	HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0002353	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0002376	PMID:20886637	PCS		12/30			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0002013	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0007928	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0025013	OMIM:245200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:245200	Krabbe disease		HP:0002191	PMID:20886637	PCS		30/30			P	HPO:skoehler[2013-08-18];HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0011096	OMIM:245200	PCS					P	HPO:probinson[2012-04-11]
OMIM:245200	Krabbe disease		HP:0002506	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0000007	PMID:8297359	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-14]
OMIM:245200	Krabbe disease		HP:0001954	OMIM:245200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:245200	Krabbe disease		HP:0002922	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0000648	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0001973	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:245200	Krabbe disease		HP:0000762	OMIM:245200	IEA					P	HPO:iea[2009-02-17]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000121	PMID:27811305	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0002003	PMID:27811305	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0004445	PMID:27811305;PMID:28089922	PCS		11/11			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15];HPO:probinson[2017-06-16]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000486	PMID:27811305	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000684	OMIM:300990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0004322	PMID:27811305;PMID:28089922	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15];HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000160	PMID:28089922	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0003097	PMID:27811305	PCS	HP:0011461	1/2			P	HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0003593	OMIM:300990	IEA					C	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001290	OMIM:300990	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0012368	PMID:27811305;PMID:28089922	PCS		3/3			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15];HPO:probinson[2017-06-16];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000518	OMIM:300990	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001903	PMID:28089922	PCS		1/1			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000678	OMIM:300990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000337	PMID:27811305	PCS					P	HPO:probinson[2017-06-16]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000219	PMID:27811305;PMID:28089922	PCS		3/3			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15];HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0006610	PMID:27811305	PCS		1/2			P	HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001643	PMID:28089922	PCS	HP:0003577	1/1			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001763	OMIM:300990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000410	OMIM:300990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001249	PMID:27811305	PCS				HP:0012825	P	HPO:probinson[2017-06-16]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000176	PMID:27811305	PCS	HP:0003577	2/2			P	HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000110	PMID:27811305	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000396	PMID:27811305	PCS					P	HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001561	PMID:27811305	PCS	HP:0030674	2/2			P	HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000494	PMID:27811305	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0410005	PMID:28089922	PCS		1/1			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001762	PMID:28089922	PCS		1/1			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001883	PMID:27811305	PCS	HP:0030674	1/2			P	HPO:probinson[2017-06-16];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000750	PMID:28089922	PCS		1/1			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001382	OMIM:300990	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000193	PMID:27811305	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000470	PMID:27811305	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0011800	OMIM:300990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0002150	PMID:27811305	PCS					P	HPO:probinson[2017-06-16]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0005280	PMID:27811305	PCS		2/2			P	HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001419	PMID:27811305	PCS					I	HPO:probinson[2017-06-16]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000407	PMID:27811305	PCS					P	HPO:probinson[2017-06-16]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000405	PMID:28089922	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0004209	PMID:27811305	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000664	PMID:28089922	PCS		1/1			P	HPO:probinson[2020-09-15];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000565	OMIM:300990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0000347	PMID:27811305	PCS		2/2			P	HPO:probinson[2017-06-16];HPO:probinson[2020-09-15]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0009836	OMIM:300990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300990	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis		HP:0001655	PMID:28089922	PCS	HP:0003577	1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-09-15]
OMIM:160010	Myoglobinuria, autosomal dominant		HP:0001919	OMIM:160010	IEA					P	HPO:iea[2009-02-17]
OMIM:160010	Myoglobinuria, autosomal dominant		HP:0003236	OMIM:160010	TAS					P	HPO:skoehler[2009-02-17]
OMIM:160010	Myoglobinuria, autosomal dominant		HP:0002913	OMIM:160010	IEA					P	HPO:iea[2009-02-17]
OMIM:160010	Myoglobinuria, autosomal dominant		HP:0001324	OMIM:160010	IEA					P	HPO:skoehler[2010-06-20]
OMIM:160010	Myoglobinuria, autosomal dominant		HP:0000006	OMIM:160010	TAS					I	HPO:skoehler[2013-05-29]
OMIM:160010	Myoglobinuria, autosomal dominant		HP:0003326	OMIM:160010	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606864	Carney-Stratakis syndrome		HP:0007378	OMIM:606864	TAS					P	HPO:skoehler[2015-01-21]
OMIM:606864	Carney-Stratakis syndrome		HP:0002668	OMIM:606864	TAS					P	HPO:skoehler[2015-01-21]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0000252	PMID:30351409	PCS		2/19			P	HPO:probinson[2019-07-06]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0000750	PMID:30351409	PCS		2/19			P	HPO:probinson[2019-07-06]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0001250	PMID:30351409	PCS	HP:0003593	19/19			P	HPO:probinson[2019-07-06]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0002373	OMIM:618482	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0002121	OMIM:618482	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0000729	PMID:30351409	PCS		3/19			P	HPO:probinson[2019-07-06]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0001263	OMIM:618482	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0003829	OMIM:618482	IEA					I	HPO:skoehler[2019-09-07]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0000006	PMID:30351409	PCS					I	HPO:probinson[2019-07-06];HPO:probinson[2019-07-06]
OMIM:618482	Generalized epilepsy with febrile seizures plus, type 10		HP:0001249	PMID:30351409	PCS		13/19			P	HPO:probinson[2019-07-06];HPO:probinson[2019-07-06]
OMIM:300984	Intellectual developmental disorder, X-linked 105		HP:0000708	PMID:25644381	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300984	Intellectual developmental disorder, X-linked 105		HP:0001344	PMID:25644381	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-27]
OMIM:300984	Intellectual developmental disorder, X-linked 105		HP:0001419	PMID:25644381	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:300984	Intellectual developmental disorder, X-linked 105		HP:0001249	PMID:25644381	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-27]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0003202	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0002089	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0000969	OMIM:253310	IEA					P	HPO:skoehler[2010-06-20]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0001560	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0004571	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0007277	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0000007	OMIM:253310	IEA					I	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0009004	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0002804	OMIM:253310	TAS					P	HPO:skoehler[2012-10-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0003811	OMIM:253310	IEA					C	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0000347	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:253310	Lethal congenital contracture syndrome 1		HP:0000765	OMIM:253310	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0003577	PMID:20829317	PCS		11/11			C	HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0000684	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000541	PMID:20829317	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0000486	PMID:20829317	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0000980	OMIM:308300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:308300	Incontinentia pigmenti		HP:0004322	OMIM:308300	PCS					P	HPO:skoehler[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0001596	PMID:20829317	PCS		2/11			P	HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0002164	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0001250	PMID:20829317	PCS		3/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0010783	OMIM:308300	TAS					P	HPO:skoehler[2013-01-22]
OMIM:308300	Incontinentia pigmenti		HP:0008070	OMIM:308300	PCS	HP:0003581				P	HPO:skoehler[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000518	PMID:20829317	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0001805	OMIM:308300	PCS					P	HPO:skoehler[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0002937	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0001807	OMIM:308300	PCS					P	HPO:skoehler[2012-03-01]
OMIM:308300	Incontinentia pigmenti		HP:0001803	OMIM:308300	PCS					P	HPO:skoehler[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0002557	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000554	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0001423	OMIM:308300	IEA					I	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0002558	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0001249	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000677	PMID:20829317	PCS		2/11			P	HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0000698	PMID:20829317	PCS		3/11			P	HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0002751	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0001000	OMIM:308300	TAS					P	HPO:skoehler[2013-01-22]
OMIM:308300	Incontinentia pigmenti		HP:0001880	OMIM:308300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0002213	OMIM:308300	PCS					P	HPO:skoehler[2012-03-01]
OMIM:308300	Incontinentia pigmenti		HP:0000252	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000573	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0003187	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000491	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0100783	OMIM:308300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:308300	Incontinentia pigmenti		HP:0100699	OMIM:308300	TAS					P	HPO:skoehler[2013-01-22]
OMIM:308300	Incontinentia pigmenti		HP:0008066	PMID:20829317	PCS		10/11			P	HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0040186	PMID:20829317	PCS		1/11			P	HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0000668	PMID:20829317	PCS		5/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-09]
OMIM:308300	Incontinentia pigmenti		HP:0007750	OMIM:308300	TAS					P	HPO:skoehler[2017-07-13]
OMIM:308300	Incontinentia pigmenti		HP:0000568	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0007850	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0004529	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000648	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0002208	OMIM:308300	TAS	HP:0011463				P	HPO:skoehler[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0005815	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0008404	OMIM:308300	TAS					P	HPO:skoehler[2013-05-03]
OMIM:308300	Incontinentia pigmenti		HP:0001257	OMIM:308300	IEA					P	HPO:iea[2009-02-17]
OMIM:308300	Incontinentia pigmenti		HP:0000962	OMIM:308300	TAS					P	HPO:skoehler[2013-01-22]
OMIM:308300	Incontinentia pigmenti		HP:0001974	OMIM:308300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000486	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001212	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000365	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0004322	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001332	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002020	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0003593	PMID:35202563	PCS					C	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0012745	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0012471	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0010296	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0012472	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0100807	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000637	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0003763	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0003764	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000252	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000494	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0031717	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000490	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0100021	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001182	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0008081	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0012583	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0007392	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000403	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002705	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0003758	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000527	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000369	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000248	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000006	PMID:35202563	PCS					I	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000582	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002002	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000463	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000185	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001270	PMID:35202563	PCS		3/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0012450	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000219	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0012171	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000455	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000974	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001028	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002650	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000750	PMID:35202563	PCS		5/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000194	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000470	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0011344	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0011228	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0100710	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0007495	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000629	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001954	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0500011	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0007018	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000742	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0005216	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000286	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002188	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001250	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001252	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001251	PMID:35202563	PCS		3/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002061	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000280	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0010761	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0031624	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000319	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000957	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000717	PMID:35202563	PCS		3/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0003307	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000713	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000278	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001763	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001249	PMID:35202563	PCS		5/5			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0025573	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002510	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001264	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000175	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0009928	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000574	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002870	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001382	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0011968	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000691	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000053	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001263	PMID:35202563	PCS		17/17			P	HPO:probinson[2022-08-21];HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000294	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0010877	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0009890	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002509	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000448	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001257	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000322	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000960	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0007359	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000325	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000687	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0005338	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0008947	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000384	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000540	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002719	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001508	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000414	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002714	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001348	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001347	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000154	PMID:35202563	PCS		4/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002212	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0008936	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000431	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002057	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000391	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000826	PMID:35202563	PCS		2/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0030051	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0002205	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0001510	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:619950	Tessadori-van Haaften neurodevelopmental syndrome 3		HP:0000303	PMID:35202563	PCS		1/17			P	HPO:probinson[2022-08-21]
OMIM:618496	Aortic valve disease 3		HP:0001650	PMID:30455415	PCS		1/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:618496	Aortic valve disease 3		HP:0001647	PMID:30455415	PCS		10/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:618496	Aortic valve disease 3		HP:0002616	PMID:30455415	PCS		11/12			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:618496	Aortic valve disease 3		HP:0001631	PMID:30455415	PCS		1/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:618496	Aortic valve disease 3		HP:0004933	PMID:30455415	PCS		1/15			P	HPO:probinson[2023-02-11]
OMIM:618496	Aortic valve disease 3		HP:0000006	PMID:30455415	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-11]
OMIM:176100	Porphyria cutanea tarda		HP:0000992	PMID:2920211	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:176100	Porphyria cutanea tarda		HP:0001596	OMIM:176100	IEA					P	HPO:iea[2009-02-17]
OMIM:176100	Porphyria cutanea tarda		HP:0001030	OMIM:176100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176100	Porphyria cutanea tarda		HP:0005586	OMIM:176100	IEA					P	HPO:iea[2009-02-17]
OMIM:176100	Porphyria cutanea tarda		HP:0001394	OMIM:176100	IEA					P	HPO:iea[2009-02-17]
OMIM:176100	Porphyria cutanea tarda		HP:0034715	OMIM:176100	TAS					P	HPO:probinson[2023-06-05]
OMIM:176100	Porphyria cutanea tarda		HP:0100324	OMIM:176100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176100	Porphyria cutanea tarda		HP:0010473	PMID:2920211	PCS		1/1			P	HPO:probinson[2022-04-22]
OMIM:176100	Porphyria cutanea tarda		HP:0001806	OMIM:176100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176100	Porphyria cutanea tarda		HP:0000007	PMID:2920211	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-04-22]
OMIM:176100	Porphyria cutanea tarda		HP:0002219	OMIM:176100	IEA					P	HPO:iea[2009-02-17]
OMIM:176100	Porphyria cutanea tarda		HP:0000006	PMID:2920211	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-22]
OMIM:176100	Porphyria cutanea tarda		HP:0001402	OMIM:176100	IEA					P	HPO:iea[2009-02-17]
OMIM:200990	Acrocallosal syndrome		HP:0001177	PMID:19619433	PCS		HP:0040281			P	HPO:iea[2009-10-22]
OMIM:200990	Acrocallosal syndrome		HP:0000286	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0001770	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2009-10-21]
OMIM:200990	Acrocallosal syndrome		HP:0000486	PMID:19619433	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000365	PMID:19619433	PCS		HP:0040283			P	HPO:iea[2009-10-22]
OMIM:200990	Acrocallosal syndrome		HP:0010803	PMID:19619433	PCS		3/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0002023	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0001250	PMID:1491747	PCS		9/27			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0002263	PMID:19619433	PCS		3/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0010808	PMID:19619433	PCS		2/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000160	PMID:19619433	PCS		2/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0003196	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2009-10-21]
OMIM:200990	Acrocallosal syndrome		HP:0001252	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0001290	PMID:1491747	PCS		20/23			P	HPO:iea[2009-10-22]
OMIM:200990	Acrocallosal syndrome		HP:0010291	PMID:19619433	PCS		1/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000639	PMID:19619433	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000319	PMID:19619433	PCS		1/59			P	HPO:iea[2009-10-22];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0012471	PMID:19619433	PCS		4/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0011220	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0000316	PMID:1491747	PCS		24/26			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0008897	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0009942	PMID:19619433	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0001841	PMID:19619433	PCS		HP:0040281			P	HPO:iea[2009-10-22]
OMIM:200990	Acrocallosal syndrome		HP:0000358	PMID:19619433	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0001249	PMID:1491747	PCS		23/25			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000054	PMID:19619433	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000494	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000175	PMID:19619433	PCS		12/59			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0005148	OMIM:200990	IEA					P	HPO:skoehler[2018-10-08]
OMIM:200990	Acrocallosal syndrome		HP:0001182	PMID:19619433	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0001537	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0006101	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2009-10-22]
OMIM:200990	Acrocallosal syndrome		HP:0000007	OMIM:200990	TAS					I	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000648	OMIM:200990	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000207	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0004209	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0009611	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0000322	PMID:19619433	PCS		18/59			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000047	PMID:1491747	PCS		10/18			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000685	PMID:19619433	PCS		1/59			P	HPO:iea[2009-10-22];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000369	OMIM:200990	TAS					P	HPO:probinson[2020-07-19]
OMIM:200990	Acrocallosal syndrome		HP:0000204	PMID:19619433	PCS		12/59			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000143	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0000384	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0006329	PMID:19619433	PCS		1/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0001671	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0000343	PMID:19619433	PCS		5/59			P	HPO:iea[2009-10-22];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000023	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0001156	OMIM:200990	TAS					P	HPO:skoehler[2014-11-26]
OMIM:200990	Acrocallosal syndrome		HP:0000260	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0001274	OMIM:200990	IEA					P	HPO:skoehler[2015-01-19]
OMIM:200990	Acrocallosal syndrome		HP:0001508	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2009-10-22]
OMIM:200990	Acrocallosal syndrome		HP:0000337	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0030680	PMID:1491747	PCS		5/22			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000218	PMID:19619433	PCS		18/59			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0002714	PMID:19619433	PCS		5/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0006335	PMID:19619433	PCS		2/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000256	PMID:1491747	PCS		25/27			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000212	PMID:19619433	PCS		1/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000377	PMID:1491747	PCS		19/23			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000154	PMID:19619433	PCS		2/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000431	PMID:1491747	PCS		24/26			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000233	PMID:19619433	PCS		5/59			P	HPO:iea[2009-10-21];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0001641	OMIM:200990	TAS					P	HPO:probinson[2017-08-27]
OMIM:200990	Acrocallosal syndrome		HP:0001162	PMID:19619433	PCS		HP:0040281			P	HPO:iea[2009-10-21]
OMIM:200990	Acrocallosal syndrome		HP:0000194	PMID:19619433	PCS		9/59			P	HPO:iea[2009-10-21];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0003781	PMID:19619433	PCS		1/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000193	PMID:19619433	PCS		2/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000190	PMID:19619433	PCS		1/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0010576	PMID:1491747	PCS		10/27			P	HPO:iea[2009-10-22]
OMIM:200990	Acrocallosal syndrome		HP:0007370	PMID:19619433;OMIM:603099	PCS		HP:0040280			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000308	PMID:19619433	PCS		8/59			P	HPO:iea[2009-10-21];HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0010066	PMID:19619433	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0007894	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:200990	Acrocallosal syndrome		HP:0001830	PMID:19619433	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0002007	PMID:1491747	PCS		23/26			P	HPO:probinson[2017-08-27]
OMIM:200990	Acrocallosal syndrome		HP:0001510	PMID:19619433	PCS		HP:0040282			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000303	PMID:19619433	PCS		1/59			P	HPO:probinson[2022-09-03]
OMIM:200990	Acrocallosal syndrome		HP:0000028	PMID:19619433	PCS		HP:0040283			P	HPO:iea[2012-04-24]
OMIM:200990	Acrocallosal syndrome		HP:0000589	OMIM:200990	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:200990	Acrocallosal syndrome		HP:0000269	OMIM:200990	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604901	North american indian childhood cirrhosis		HP:0001409	PMID:12417987	IEA					P	HPO:probinson[2013-02-23]
OMIM:604901	North american indian childhood cirrhosis		HP:0000007	PMID:12417987	IEA					I	HPO:probinson[2013-01-09]
OMIM:604901	North american indian childhood cirrhosis		HP:0002613	PMID:12417987	IEA					P	HPO:probinson[2013-02-23]
OMIM:604901	North american indian childhood cirrhosis		HP:0006579	PMID:12417987	IEA					P	HPO:probinson[2013-02-23]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0000252	OMIM:121070	TAS				HP:0012825	P	HPO:probinson[2010-06-20]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0003577	PMID:7039311	PCS					C	HPO:probinson[2022-06-26]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0001762	OMIM:121070	IEA					P	HPO:iea[2009-02-17]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0000211	OMIM:121070	TAS					P	HPO:skoehler[2017-07-13]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0000160	OMIM:121070	IEA					P	HPO:iea[2009-02-17]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0005684	OMIM:121070	TAS					P	HPO:probinson[2009-02-17]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0009473	OMIM:121070	TAS				HP:0012828	P	HPO:probinson[2012-05-27]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0008366	OMIM:121070	TAS					P	HPO:probinson[2022-06-26]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0040196	OMIM:121070	TAS					P	HPO:skoehler[2015-10-05]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0011234	OMIM:121070	TAS					P	HPO:probinson[2009-02-17]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0000006	OMIM:121070	IEA					I	HPO:iea[2009-02-17]
OMIM:121070	Arthrogryposis, distal, type 2E		HP:0000347	OMIM:121070	IEA					P	HPO:iea[2009-02-17]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003236	PMID:35617047	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003596	PMID:35617047	PCS		2/5			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003198	PMID:35617047	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003690	PMID:35617047	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0030319	PMID:35617047	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0031964	PMID:35617047	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0007141	PMID:35617047	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0011463	PMID:35617047	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0011462	PMID:35617047	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003327	PMID:35617047	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0002579	PMID:35617047	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0002018	PMID:35617047	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003688	PMID:35617047	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0001249	PMID:35617047	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0002578	PMID:35617047	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003689	PMID:35617047	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003202	PMID:35617047	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003687	PMID:35617047	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0002015	PMID:35617047	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0031956	PMID:35617047	PCS		0/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003621	PMID:35617047	PCS		1/5			C	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0003200	PMID:35617047	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0002013	PMID:35617047	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0001284	PMID:35617047	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0000407	PMID:35617047	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0000508	PMID:35617047	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0000602	PMID:35617047	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0000007	PMID:35617047	PCS					I	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0002505	PMID:35617047	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0000006	PMID:35617047	PCS					I	HPO:probinson[2024-05-02]
OMIM:620647	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6		HP:0004326	PMID:35617047	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-02]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0002465	OMIM:615824	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000286	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000582	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001250	PMID:28804536;PMID:24385928	PCS		2/2			P	HPO:probinson[2022-10-01];HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001252	PMID:28804536	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001508	PMID:28804536	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000718	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0008314	PMID:24385928	PCS		0/1			P	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000752	OMIM:615824	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001942	OMIM:615824	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001623	PMID:28804536	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0003623	PMID:28804536;PMID:24385928	PCS		2/2			C	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0003128	PMID:28804536	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001562	PMID:28804536	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0002133	PMID:28804536	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0002013	PMID:28804536	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0011924	PMID:24385928	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0002151	PMID:24385928	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001263	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0002490	PMID:24385928	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0011923	PMID:24385928	PCS		1/1			P	HPO:probinson[2022-10-01];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0005280	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0100259	OMIM:615824	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000407	PMID:24385928	PCS		1/1		HP:0012825	P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000007	PMID:24385928	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001319	PMID:28804536	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0008347	PMID:24385928	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0004902	PMID:24385928	PCS	HP:0003623	1/1			P	HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000664	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0001511	PMID:28804536;PMID:24385928	PCS		2/2			P	HPO:probinson[2022-10-01];HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0002049	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:615824	Mitochondrial complex III deficiency, nuclear type 7		HP:0000028	PMID:24385928	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-10-01]
OMIM:614284	Stickler syndrome, type V		HP:0000541	PMID:21671392	PCS		8/8			P	HPO:skoehler[2012-10-17]
OMIM:614284	Stickler syndrome, type V		HP:0004322	PMID:21671392	PCS		8/8			P	HPO:skoehler[2018-10-08]
OMIM:614284	Stickler syndrome, type V		HP:0000331	PMID:21671392	PCS		8/8			P	HPO:probinson[2023-03-23]
OMIM:614284	Stickler syndrome, type V		HP:0000518	PMID:21671392	PCS		0/8			P	HPO:probinson[2023-03-23]
OMIM:614284	Stickler syndrome, type V		HP:0000407	PMID:21671392	PCS		8/8			P	HPO:skoehler[2017-07-13]
OMIM:614284	Stickler syndrome, type V		HP:0011463	PMID:21671392	PCS					C	HPO:probinson[2023-03-23]
OMIM:614284	Stickler syndrome, type V		HP:0007773	PMID:21671392	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-23]
OMIM:614284	Stickler syndrome, type V		HP:0000007	PMID:21671392	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-23]
OMIM:614284	Stickler syndrome, type V		HP:0011800	PMID:21671392	PCS		8/8			P	HPO:probinson[2023-03-23]
OMIM:614284	Stickler syndrome, type V		HP:0011003	PMID:21671392	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-23]
OMIM:614284	Stickler syndrome, type V		HP:0000201	PMID:21671392	PCS		0/8			P	HPO:probinson[2023-03-23]
OMIM:605389	Hypotrichosis 1		HP:0000164	PMID:20393562	PCS		0/19			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-02]
OMIM:605389	Hypotrichosis 1		HP:0001597	PMID:20393562	PCS		0/19			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-02];HPO:probinson[2023-04-09]
OMIM:605389	Hypotrichosis 1		HP:0002231	PMID:20393562	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-02]
OMIM:605389	Hypotrichosis 1		HP:0011463	PMID:20393562	PCS					C	HPO:probinson[2022-11-02]
OMIM:605389	Hypotrichosis 1		HP:0000653	PMID:20393562	PCS		0/19			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-09]
OMIM:605389	Hypotrichosis 1		HP:0045075	PMID:20393562	PCS		0/19			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-09]
OMIM:605389	Hypotrichosis 1		HP:0008070	PMID:20393562	PCS	HP:0011463	19/19			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-11-02];HPO:probinson[2023-04-09]
OMIM:605389	Hypotrichosis 1		HP:0000006	PMID:20393562	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2022-11-02]
OMIM:605389	Hypotrichosis 1		HP:0002225	PMID:20393562	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-09]
OMIM:605389	Hypotrichosis 1		HP:0002215	PMID:20393562	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-09]
OMIM:605389	Hypotrichosis 1		HP:0000951	PMID:20393562	PCS		0/19			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-02]
OMIM:620121	Iron overload, susceptibility to		HP:0012463	PMID:26582087	PCS		4/8			P	HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0003596	PMID:26582087	PCS		6/8			C	HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0012465	PMID:26582087	PCS					P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0002829	PMID:26582087	PCS		2/8			P	HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0003584	PMID:26582087	PCS		2/8			C	HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0003281	PMID:26582087	PCS		8/8			P	HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0005978	PMID:26582087	PCS		1/8			P	HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0000006	PMID:26582087	PCS					I	HPO:probinson[2023-01-19]
OMIM:620121	Iron overload, susceptibility to		HP:0031877	PMID:26582087	PCS		4/6			P	HPO:probinson[2023-01-19]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0001596	PMID:25712130	PCS		0/2			P	HPO:probinson[2022-06-20]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0011463	PMID:25712130	PCS		2/2			C	HPO:probinson[2022-06-20]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0008066	PMID:25712130	PCS	HP:0011463	2/2			P	HPO:probinson[2022-06-20]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0000007	PMID:25712130	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-20]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0000989	PMID:25712130	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0008404	PMID:25712130	PCS		2/2			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-06-20]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0007556	PMID:25712130	PCS		2/2			P	HPO:skoehler[2015-08-02];HPO:probinson[2022-06-20]
OMIM:616487	Epidermolysis bullosa simplex with nail dystrophy		HP:0034193	PMID:25712130	PCS		2/2			P	HPO:probinson[2022-06-20]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0003016	OMIM:617941	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0004322	PMID:28331068	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001252	PMID:28331068	PCS		5/6			P	HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0002240	PMID:28331068	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0003593	PMID:28331068	PCS		5/6			C	HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0008151	PMID:28331068	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001508	PMID:28331068	PCS		5/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0002719	PMID:28331068	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001607	PMID:28331068	PCS		HP:0040284			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0011463	PMID:28331068	PCS		1/6			C	HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0006276	PMID:28331068	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0000218	PMID:28331068	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001522	PMID:28331068	PCS		1/6			C	HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001601	PMID:28331068	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0003645	PMID:28331068	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0002014	PMID:28331068	PCS		5/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0000252	PMID:28331068	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0002970	PMID:28331068	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0003025	PMID:28331068	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001263	PMID:28331068	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0002570	PMID:28331068	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0011003	PMID:28331068	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0000907	PMID:28331068	PCS		4/4			P	HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0003819	PMID:28331068	PCS		2/6			C	HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001738	PMID:28331068	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0000007	PMID:28331068	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001873	PMID:28331068	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0000369	PMID:28331068	PCS		4/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001875	PMID:28331068	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:617941	Shwachman-Diamond syndrome 2		HP:0001897	PMID:28331068	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-15]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0001562	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0006989	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0001640	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0012707	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0012708	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0011923	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0001518	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0034198	PMID:33502047	PCS		1/1			C	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0001903	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0001639	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0011682	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0000007	PMID:33502047	PCS					I	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0001511	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0000047	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0001631	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0000028	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:620135	Mitochondrial complex I deficiency, nuclear type 39		HP:0003128	PMID:33502047	PCS		1/1			P	HPO:probinson[2022-12-12]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002421	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002069	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000483	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000486	PMID:29100089	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002540	OMIM:617799	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0004322	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001250	PMID:29100089	PCS		4/20			P	HPO:probinson[2022-06-03];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002384	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001252	PMID:29100089	PCS		6/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000680	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002020	PMID:29100089	PCS		2/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001251	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0003593	PMID:29100089	PCS		4/10			C	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002061	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000639	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000958	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0011220	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000718	PMID:29100089	PCS		2/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000678	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001605	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002579	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001249	PMID:29100089	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0003763	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000252	PMID:29100089	PCS		5/10			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000970	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001344	PMID:29100089	PCS		3/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000331	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0011968	PMID:29100089	PCS		1/10			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000490	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001263	PMID:29100089	PCS		8/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0011800	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0011445	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0100660	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001816	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000729	PMID:29100089	PCS		2/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000964	PMID:29100089	PCS		2/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000565	PMID:29100089	PCS		2/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000006	PMID:29100089	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002104	PMID:29100089	PCS		3/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000687	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000341	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002883	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002487	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000340	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0003577	PMID:29100089	PCS		6/10			C	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001272	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0008070	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000737	PMID:29100089	PCS		4/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000817	PMID:29100089	PCS		3/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0012450	PMID:29100089	PCS		4/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0025116	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000016	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0008936	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000750	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0002376	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0010819	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0004396	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0032988	PMID:29100089	PCS		2/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001518	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0500093	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0000505	OMIM:617799	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001510	PMID:29100089	PCS		2/10			P	HPO:probinson[2022-06-03]
OMIM:617799	Intellectual developmental disorder, autosomal dominant 54		HP:0001875	PMID:29100089	PCS		1/10			P	HPO:probinson[2022-06-03]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0004324	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0001596	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0025383	OMIM:615830	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0001030	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0001061	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000819	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000939	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000716	OMIM:615830	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000938	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0008221	OMIM:615830	TAS				HP:0012832	P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000822	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000712	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000978	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0003118	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0003701	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0500011	OMIM:615830	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0001579	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0001007	OMIM:615830	TAS					P	HPO:skoehler[2014-08-24]
OMIM:615830	Pigmented nodular adrenocortical disease, primary, 4		HP:0000006	OMIM:615830	TAS					I	HPO:skoehler[2015-12-30]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000582	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001250	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001252	PMID:37880421	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0005274	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0011463	PMID:37880421	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000718	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000238	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000219	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001302	PMID:37880421	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001324	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001249	PMID:37880421	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000358	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001347	PMID:37880421	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000750	PMID:37880421	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0009905	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0002376	PMID:37880421	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001263	PMID:37880421	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0010751	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000729	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000007	PMID:37880421	PCS					I	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000648	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0000664	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0001257	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0007018	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:620653	Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly		HP:0007933	PMID:37880421	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-01]
OMIM:618643	Spermatogenic failure 39		HP:0032560	PMID:31178125	PCS					P	HPO:probinson[2020-07-22]
OMIM:618643	Spermatogenic failure 39		HP:0003251	PMID:31178125	PCS		5/5			P	HPO:probinson[2020-07-22]
OMIM:618643	Spermatogenic failure 39		HP:0011462	PMID:31178125	PCS		5/5			C	HPO:probinson[2022-05-14]
OMIM:618643	Spermatogenic failure 39		HP:0032562	PMID:31178125	PCS					P	HPO:probinson[2020-07-22]
OMIM:618643	Spermatogenic failure 39		HP:0000007	PMID:31178125	PCS					I	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:618643	Spermatogenic failure 39		HP:0012207	PMID:31178125	PCS		15/15			P	HPO:probinson[2020-07-22]
OMIM:618643	Spermatogenic failure 39		HP:0032558	PMID:31178125	PCS					P	HPO:probinson[2020-07-22]
OMIM:618643	Spermatogenic failure 39		HP:0000798	PMID:31178125	PCS					P	HPO:probinson[2020-07-22]
OMIM:618643	Spermatogenic failure 39		HP:0032559	PMID:31178125	PCS					P	HPO:probinson[2020-07-22]
OMIM:300589	Nystagmus 5, congenital, X-linked		HP:0000484	OMIM:300589	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300589	Nystagmus 5, congenital, X-linked		HP:0000486	OMIM:300589	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300589	Nystagmus 5, congenital, X-linked		HP:0000639	OMIM:300589	TAS	HP:0003593				P	HPO:skoehler[2012-10-14]
OMIM:300589	Nystagmus 5, congenital, X-linked		HP:0001423	OMIM:300589	TAS					I	HPO:skoehler[2012-10-14]
OMIM:300589	Nystagmus 5, congenital, X-linked		HP:0011515	OMIM:300589	TAS					P	HPO:skoehler[2012-10-14]
OMIM:190650	Triphalangeal thumbs and dislocation of patella		HP:0001199	OMIM:190650	IEA					P	HPO:iea[2009-02-17]
OMIM:190650	Triphalangeal thumbs and dislocation of patella		HP:0004322	OMIM:190650	IEA					P	HPO:iea[2009-02-17]
OMIM:190650	Triphalangeal thumbs and dislocation of patella		HP:0005001	OMIM:190650	TAS					P	HPO:skoehler[2009-02-17]
OMIM:190650	Triphalangeal thumbs and dislocation of patella		HP:0000006	OMIM:190650	IEA					I	HPO:iea[2009-02-17]
OMIM:114550	Hepatocellular carcinoma		HP:0001442	OMIM:114550	TAS					I	HPO:probinson[2009-02-17]
OMIM:114550	Hepatocellular carcinoma		HP:0006572	OMIM:114550	TAS					P	HPO:probinson[2009-02-17]
OMIM:114550	Hepatocellular carcinoma		HP:0001402	OMIM:114550	TAS					P	HPO:probinson[2009-02-17]
OMIM:114550	Hepatocellular carcinoma		HP:0001413	OMIM:114550	TAS					P	HPO:probinson[2009-02-17]
OMIM:615401	Immunodeficiency 8		HP:0410300	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0002783	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0001263	OMIM:615401	TAS					P	HPO:skoehler[2013-09-30]
OMIM:615401	Immunodeficiency 8		HP:0410295	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0003593	PMID:19097825	PCS		1/1			C	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0002020	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0009098	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:4000166	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-03-31]
OMIM:615401	Immunodeficiency 8		HP:0001888	PMID:19097825	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0000007	PMID:19097825	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0000403	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0002788	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0007018	PMID:19097825	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:615401	Immunodeficiency 8		HP:0002721	PMID:19097825	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-02-11]
OMIM:613070	Liver failure, infantile, transient		HP:0001252	OMIM:613070	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613070	Liver failure, infantile, transient		HP:0002240	PMID:19732863	PCS		13/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0003593	PMID:19732863	PCS		10/13			C	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0001290	OMIM:613070	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613070	Liver failure, infantile, transient		HP:0003073	PMID:19732863	PCS		13/13			P	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0003270	PMID:19732863	PCS		13/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0031964	PMID:19732863	PCS		12/12			P	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0008151	PMID:19732863	PCS		8/8			P	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0000737	PMID:19732863	PCS	HP:0003593	13/13			P	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0200125	PMID:19732863	PCS		2/2			P	HPO:skoehler[2013-06-11];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0008872	PMID:19732863	PCS	HP:0003593	13/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0003648	PMID:19732863	PCS		13/13			P	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0006554	PMID:19732863	PCS	HP:0003593	13/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0001522	PMID:19732863	PCS		4/13			C	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0002910	OMIM:613070	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613070	Liver failure, infantile, transient		HP:0000952	PMID:19732863	PCS	HP:0003593	13/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0001403	PMID:19732863	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0004315	PMID:19732863	PCS		5/7			P	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0003128	PMID:19732863	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0003623	PMID:19732863	PCS		3/13			C	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0002013	PMID:19732863	PCS	HP:0003593	13/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0002151	PMID:19732863	PCS		12/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0008160	PMID:19732863	PCS		13/13			P	HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0002904	PMID:19732863	PCS		10/11			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0000007	PMID:19732863	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-09-11]
OMIM:613070	Liver failure, infantile, transient		HP:0001414	OMIM:613070	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613070	Liver failure, infantile, transient		HP:0003215	PMID:19732863	PCS		13/13			P	HPO:probinson[2022-09-11]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000582	PMID:24916380	PCS		3/3		HP:0012825	P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0007737	PMID:24916380	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000662	PMID:24916380	PCS	HP:0003621	3/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000430	PMID:24916380	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0004322	PMID:24916380	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0009907	PMID:24916380	PCS		2/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0001263	PMID:24916380	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000272	PMID:24916380	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000518	PMID:24916380	PCS	HP:0003621	3/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0011463	PMID:24916380	PCS		3/3			C	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000689	PMID:24916380	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000007	PMID:24916380	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000510	PMID:24916380	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0007843	PMID:24916380	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0007722	PMID:24916380	PCS		3/3			P	HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000556	PMID:24916380	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-02-12]
OMIM:616108	Retinal dystrophy, juvenile cataracts, and short stature syndrome		HP:0000687	PMID:24916380	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-02-12]
OMIM:110050	Blepharonasofacial malformation syndrome		HP:0010628	OMIM:110050	IEA					P	HPO:iea[2009-02-17]
OMIM:110050	Blepharonasofacial malformation syndrome		HP:0000298	OMIM:110050	IEA					P	HPO:iea[2009-02-17]
OMIM:110050	Blepharonasofacial malformation syndrome		HP:0000506	OMIM:110050	IEA					P	HPO:iea[2009-02-17]
OMIM:110050	Blepharonasofacial malformation syndrome		HP:0000006	OMIM:110050	IEA					I	HPO:iea[2009-02-17]
OMIM:110050	Blepharonasofacial malformation syndrome		HP:0001249	OMIM:110050	IEA					P	HPO:iea[2009-02-17]
OMIM:110050	Blepharonasofacial malformation syndrome		HP:0001304	OMIM:110050	IEA					P	HPO:iea[2009-02-17]
OMIM:223350	Dohle bodies and leukemia		HP:0040235	PMID:5280989	PCS					P	HPO:lccarmody[2018-11-06]
OMIM:223350	Dohle bodies and leukemia		HP:0001684	PMID:5280989	PCS					P	HPO:lccarmody[2018-11-06]
OMIM:223350	Dohle bodies and leukemia		HP:0001903	PMID:5280989	IEA					P	HPO:skoehler[2010-06-20];HPO:lccarmody[2018-11-06]
OMIM:223350	Dohle bodies and leukemia		HP:0004808	PMID:5280989	PCS					P	HPO:lccarmody[2018-11-06]
OMIM:223350	Dohle bodies and leukemia		HP:0000007	OMIM:223350	IEA					I	HPO:iea[2009-02-17]
OMIM:223350	Dohle bodies and leukemia		HP:0001954	PMID:5280989	PCS					P	HPO:lccarmody[2018-11-06]
OMIM:223350	Dohle bodies and leukemia		HP:0001004	PMID:5280989	PCS					P	HPO:lccarmody[2018-11-06]
OMIM:618131	Immunodeficiency 58		HP:0004322	PMID:27896283	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0410135	PMID:27647349	PCS		1/6			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002583	PMID:29479355	PCS		1/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0001051	PMID:27647349	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0003394	PMID:27896283	PCS		3/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0001075	PMID:27647349	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0003593	PMID:29479355	PCS		1/7			C	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0003193	PMID:29479355	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0012203	PMID:27647349	PCS		1/6			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0031292	PMID:27896283	PCS		1/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0032140	PMID:28112205	PCS					P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0001508	PMID:28112205	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0032163	PMID:27896283;PMID:27647349	PCS		4/10			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0011463	PMID:29479355	PCS		5/7			C	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0006510	PMID:27896283	PCS		2/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0006532	PMID:27896283	PCS		2/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0001742	PMID:27896283	PCS		3/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0200043	PMID:29479355;PMID:27896283	PCS		8/15			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0003623	PMID:29479355	PCS		1/7			C	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0004313	PMID:27896283	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002015	PMID:29479355	PCS		5/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0000992	PMID:27896283	PCS		2/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0005202	PMID:27647349	PCS		1/6			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002099	PMID:29479355;PMID:27896283;PMID:27647349	PCS		8/17			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002110	PMID:29479355;PMID:27647349	PCS		6/13			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0012378	PMID:27896283	PCS		2/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0011107	PMID:27896283	PCS		3/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0100633	PMID:29479355	PCS		5/7			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0008064	PMID:27647349	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002728	PMID:27647349	PCS		3/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0040189	PMID:27647349	PCS		3/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0025526	PMID:27896283	PCS		4/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0000007	PMID:27647349	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0000964	PMID:29479355;PMID:27896283	PCS		11/15			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0100518	PMID:27896283	PCS		2/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0100838	PMID:29479355	PCS		7/7			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0005419	PMID:28112205	PCS					P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0000389	PMID:29479355	PCS		2/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002205	PMID:29479355;PMID:27896283;PMID:27647349	PCS		11/17			P	HPO:skoehler[2019-04-18];HPO:probinson[2020-11-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002788	PMID:27896283	PCS		2/4			P	HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0004469	PMID:27647349	PCS		1/6			P	HPO:skoehler[2019-02-15];HPO:probinson[2020-11-15]
OMIM:618131	Immunodeficiency 58		HP:0002028	PMID:29479355;PMID:27896283	PCS		4/15			P	HPO:probinson[2020-11-15]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001650	OMIM:615415	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001562	PMID:26862157;PMID:23418306	PCS		3/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001396	OMIM:615415	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0003577	OMIM:615415	TAS					C	HPO:skoehler[2013-09-30]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001660	PMID:23418306	PCS		2/3			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0002980	PMID:26862157;PMID:23418306	PCS		3/3			P	HPO:probinson[2022-11-26];HPO:probinson[2022-11-26];HPO:skoehler[2013-10-22];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0002089	PMID:23418306	PCS		1/3			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001696	PMID:23418306	PCS		1/3			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001762	PMID:23418306	PCS		1/3			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0002101	PMID:23418306	PCS		1/3			P	HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001395	OMIM:615415	TAS					P	HPO:skoehler[2013-09-30]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0002240	OMIM:615415	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0002280	PMID:26862157	PCS		1/1			P	HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001639	OMIM:615415	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0034198	PMID:23418306	PCS		3/3			C	HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001746	PMID:23418306	PCS		1/3			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0000800	PMID:26862157;PMID:23418306	PCS		3/4			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0003826	PMID:26862157;PMID:23418306	PCS		2/2			C	HPO:skoehler[2014-01-28];HPO:probinson[2022-11-26];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0000007	PMID:23418306	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0006563	PMID:23418306	PCS		2/2			P	HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001407	PMID:23418306	PCS		2/3			P	HPO:probinson[2022-11-26]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0001642	OMIM:615415	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615415	Renal-Hepatic-Pancreatic dysplasia 2		HP:0000105	PMID:23418306	PCS		2/3			P	HPO:skoehler[2013-09-30];HPO:probinson[2022-11-26]
OMIM:613702	Klippel-Feil syndrome 3, autosomal dominant		HP:6000807	PMID:17023841	PCS					P	HPO:probinson[2024-08-03]
OMIM:613702	Klippel-Feil syndrome 3, autosomal dominant		HP:0000612	PMID:19864492	PCS					P	HPO:probinson[2017-12-13]
OMIM:613702	Klippel-Feil syndrome 3, autosomal dominant		HP:0030281	PMID:19864492	PCS					P	HPO:probinson[2017-12-13]
OMIM:613702	Klippel-Feil syndrome 3, autosomal dominant		HP:0002943	PMID:19864492	PCS					P	HPO:probinson[2017-12-13]
OMIM:613702	Klippel-Feil syndrome 3, autosomal dominant		HP:0000006	PMID:19864492	PCS					I	HPO:probinson[2013-06-02]
OMIM:613702	Klippel-Feil syndrome 3, autosomal dominant		HP:0004635	OMIM:613702	TAS					P	HPO:probinson[2013-06-02]
OMIM:613702	Klippel-Feil syndrome 3, autosomal dominant		HP:0000567	PMID:19864492	PCS					P	HPO:probinson[2017-12-13]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0002015	OMIM:603511	IEA					P	HPO:iea[2009-02-17]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003236	OMIM:603511	IEA					P	HPO:iea[2009-02-17]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0010628	OMIM:603511	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003555	OMIM:603511	TAS					P	HPO:probinson[2009-02-17]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0001283	OMIM:603511	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0001371	OMIM:603511	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003551	PMID:22334415	PCS		6/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003560	PMID:22334415	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0002094	OMIM:603511	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003391	PMID:22334415	PCS		2/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0033383	PMID:22334415	PCS		2/2			P	HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0011462	PMID:22334415	PCS		9/9			C	HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0009046	PMID:22334415	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003749	PMID:22334415	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003805	PMID:22334415	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0002515	PMID:22334415	PCS		4/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0002505	PMID:22334415	PCS		5/9			P	HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003547	PMID:22334415	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0000006	PMID:22334415	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003677	PMID:22334415	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-08-28]
OMIM:603511	Muscular dystrophy, limb-girdle, type 1E		HP:0003326	PMID:22334415	PCS		1/9			P	HPO:probinson[2022-08-28]
OMIM:227650	Fanconi anemia		HP:0003213	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0003214	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000365	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000486	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0004322	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000086	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0003251	PMID:29904161	TAS		HP:0040284			P	HPO:nvasilevsky[2019-05-14];HPO:nvasilevsky[2019-05-14]
OMIM:227650	Fanconi anemia		HP:0000085	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000081	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0012210	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001909	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000815	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000957	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001903	OMIM:227650	TAS					P	HPO:skoehler[2012-10-17]
OMIM:227650	Fanconi anemia		HP:0030680	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000978	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001627	OMIM:227650	TAS					P	HPO:skoehler[2015-12-30]
OMIM:227650	Fanconi anemia		HP:0009943	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001249	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000252	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001000	OMIM:227650	TAS					P	HPO:skoehler[2014-03-24]
OMIM:227650	Fanconi anemia		HP:0003221	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001518	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000568	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000007	OMIM:227650	TAS					I	HPO:skoehler[2017-07-13]
OMIM:227650	Fanconi anemia		HP:0009777	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001896	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0009778	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001873	OMIM:227650	TAS					P	HPO:skoehler[2012-10-17]
OMIM:227650	Fanconi anemia		HP:0000028	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001876	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0003974	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0000104	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001017	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:227650	Fanconi anemia		HP:0001875	OMIM:227650	IEA					P	HPO:iea[2009-02-17]
OMIM:615373	Left ventricular noncompaction 8		HP:0003621	PMID:23768516	PCS		2/3			C	HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0025169	PMID:23768516	PCS		2/3			P	HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0011462	PMID:23768516	PCS		1/3			C	HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0025168	PMID:23768516	PCS		1/3			P	HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0030682	PMID:23768516	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0001635	PMID:23768516	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0011675	PMID:23768516	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0001653	PMID:23768516	PCS		1/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0000006	PMID:23768516	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-07-03]
OMIM:615373	Left ventricular noncompaction 8		HP:0001644	PMID:23768516	PCS		1/3			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-07-03]
OMIM:619549	Immunodeficiency 86, mycobacteriosis		HP:0003203	PMID:30127434	PCS		0/1			P	HPO:probinson[2022-01-23]
OMIM:619549	Immunodeficiency 86, mycobacteriosis		HP:0020086	PMID:30127434	PCS		3/3			P	HPO:probinson[2022-01-23]
OMIM:619549	Immunodeficiency 86, mycobacteriosis		HP:0003496	PMID:30127434	PCS		2/3			P	HPO:probinson[2022-01-23]
OMIM:619549	Immunodeficiency 86, mycobacteriosis		HP:0000007	PMID:30127434	PCS					I	HPO:probinson[2022-01-23]
OMIM:619549	Immunodeficiency 86, mycobacteriosis		HP:0004315	PMID:30127434	PCS		3/3			P	HPO:probinson[2022-01-23]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0004325	PMID:28198391	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0012583	PMID:28198391	PCS		1/1			P	HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0000160	PMID:28198391	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0012471	PMID:28198391	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0008551	PMID:28198391	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0003593	PMID:28198391	PCS		1/1			C	HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0000007	PMID:28198391	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0011126	PMID:28198391	PCS		1/1			P	HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0001511	PMID:28198391	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0008689	PMID:28198391	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0000369	PMID:28198391	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-14]
OMIM:617564	Meier-Gorlin syndrome 8		HP:0000347	PMID:28198391	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-14]
OMIM:222700	Lysinuric protein intolerance		HP:0003774	OMIM:222700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0003355	OMIM:222700	TAS					P	HPO:skoehler[2015-01-21]
OMIM:222700	Lysinuric protein intolerance		HP:0004322	OMIM:222700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0003297	PMID:10080182	PCS		10/10			P	HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0001252	PMID:10080182	PCS		4/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0002240	PMID:10080182	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0003593	PMID:10080182	PCS		10/10			C	HPO:probinson[2012-03-25];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0008070	OMIM:222700	TAS					P	HPO:skoehler[2012-03-01]
OMIM:222700	Lysinuric protein intolerance		HP:0000939	PMID:10080182	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0012156	OMIM:222700	TAS					P	HPO:skoehler[2013-01-22]
OMIM:222700	Lysinuric protein intolerance		HP:0500142	PMID:10080182	PCS		10/10			P	HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0001508	PMID:10080182	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0001903	OMIM:222700	IEA		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0001987	OMIM:222700	TAS					P	HPO:probinson[2012-03-25]
OMIM:222700	Lysinuric protein intolerance		HP:0002757	OMIM:222700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:222700	Lysinuric protein intolerance		HP:0001324	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0002018	PMID:10080182	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0000974	OMIM:222700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:222700	Lysinuric protein intolerance		HP:0001249	PMID:10080182	PCS		2/4			P	HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0002038	PMID:10080182	PCS		9/10			P	HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0001744	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0000973	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0002014	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0003202	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0002213	OMIM:222700	TAS					P	HPO:probinson[2012-03-25]
OMIM:222700	Lysinuric protein intolerance		HP:0006517	OMIM:222700	TAS					P	HPO:skoehler[2014-06-24]
OMIM:222700	Lysinuric protein intolerance		HP:0002750	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0001882	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0002013	PMID:10080182	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0001263	PMID:10080182	PCS		10/10			P	HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0002151	OMIM:222700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:222700	Lysinuric protein intolerance		HP:0004395	OMIM:222700	TAS					P	HPO:skoehler[2013-01-22]
OMIM:222700	Lysinuric protein intolerance		HP:0003281	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0002093	OMIM:222700	IEA		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0040223	OMIM:222700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:222700	Lysinuric protein intolerance		HP:0000007	PMID:10080182	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-05-20]
OMIM:222700	Lysinuric protein intolerance		HP:0000725	OMIM:222700	TAS		HP:0040283			P	HPO:probinson[2012-03-25]
OMIM:222700	Lysinuric protein intolerance		HP:0001956	OMIM:222700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0003218	OMIM:222700	TAS					P	HPO:probinson[2012-03-25]
OMIM:222700	Lysinuric protein intolerance		HP:0001873	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0001733	OMIM:222700	IEA					P	HPO:iea[2009-02-17]
OMIM:222700	Lysinuric protein intolerance		HP:0001259	OMIM:222700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000286	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0001276	PMID:23487782	PCS		2/3			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0006109	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000483	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0003577	PMID:23487782	PCS		3/3			C	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000563	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000486	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000540	PMID:23487782	PCS		3/3			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0004322	PMID:23487782	PCS		3/3			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0003199	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000581	PMID:23487782	PCS		1/3			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0008052	PMID:23487782	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0006251	PMID:23487782	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0032342	PMID:23487782	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0003725	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0030084	OMIM:108145	TAS					P	HPO:skoehler[2014-09-21]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000218	PMID:23487782	PCS		3/3			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000411	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0009921	PMID:23487782	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000512	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0001249	PMID:23487782	PCS		0/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0003546	PMID:23487782	PCS		2/2			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0002875	PMID:23487782	PCS		3/3			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0007703	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0001166	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0001265	PMID:23487782	PCS		3/3			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0002650	PMID:23487782	PCS		1/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0004673	PMID:23487782	PCS		6/6			P	HPO:probinson[2023-02-11];HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000490	PMID:23487782	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0005684	PMID:23487782	PCS	HP:0003577	3/3			P	HPO:probinson[2012-07-16];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0005001	PMID:23487782	PCS		1/2			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0002091	PMID:23487782	PCS		3/3			P	HPO:skoehler[2014-02-06];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0006184	PMID:23487782	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0002808	PMID:23487782	PCS		3/3			P	HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000508	PMID:23487782	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0001119	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000602	PMID:23487782	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000767	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0005879	PMID:23487782	PCS	HP:0003577	3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000006	PMID:23487782	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0000325	OMIM:108145	IEA					P	HPO:iea[2009-02-17]
OMIM:108145	Arthrogryposis, distal, type 5		HP:0001776	PMID:23487782	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0002465	PMID:26544804	PCS					P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000286	PMID:26544804	PCS		3/15			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0003577	PMID:26544804	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000582	PMID:26544804	PCS		1/15			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000486	PMID:26544804	PCS		6/15			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000343	PMID:26544804	PCS		4/15			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000365	PMID:26544804	PCS		2/14			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001772	PMID:26544804	PCS		3/16			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0003396	PMID:26544804	PCS		2/4			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0004684	PMID:26544804	PCS		4/16			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0002066	PMID:26544804	PCS		8/14			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001252	PMID:26544804	PCS	HP:0003593	15/17			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001508	PMID:26544804	PCS		11/17			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001629	PMID:26544804	PCS		3/17			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000319	PMID:26544804	PCS		1/15			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0012450	PMID:26544804	PCS		8/11			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0002616	PMID:26544804	PCS		3/17			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001647	PMID:26544804	PCS		2/17			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0002936	PMID:26544804	PCS					P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000219	PMID:26544804	PCS		6/15			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0002317	PMID:26544804	PCS					P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000218	PMID:26544804	PCS		4/13			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001763	PMID:26544804	PCS		3/16			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001249	PMID:26544804	PCS					P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0007108	PMID:26544804	PCS		9/12			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0002136	PMID:26544804	PCS		2/17			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000494	PMID:26544804	PCS		6/15			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000750	PMID:26544804	PCS		15/15			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0031936	PMID:26544804	PCS		11/13			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0011968	PMID:26544804	PCS		12/13			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001382	PMID:26544804	PCS		5/12			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001263	PMID:26544804	PCS		17/17			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001284	PMID:26544804	PCS		12/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0010535	PMID:26544804	PCS		4/8			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001719	PMID:26544804	PCS		1/17			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0004209	PMID:26544804	PCS		3/15			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0001852	PMID:26544804	PCS		1/17			P	HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000762	PMID:26544804	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000006	PMID:26544804	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000325	PMID:26544804	PCS		6/16			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:616652	Yuan-Harel-Lupski syndrome		HP:0000445	PMID:26544804	PCS		9/15			P	HPO:skoehler[2015-11-29];HPO:probinson[2022-11-24]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0002421	PMID:33131106	PCS		2/4			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0032989	PMID:33131106	PCS		2/3			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0002521	PMID:33131106	PCS		3/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0000750	PMID:33131106	PCS		5/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0002540	PMID:33131106	PCS		2/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0031936	PMID:33131106	PCS		3/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0001250	PMID:33131106	PCS		4/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0001252	PMID:33131106	PCS		2/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0003593	PMID:33131106	PCS		3/4			C	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0033128	PMID:33131106	PCS		3/4			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0011097	PMID:33131106	PCS		1/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0000639	PMID:33131106	PCS		1/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0000729	PMID:33131106	PCS		4/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0200134	PMID:33131106	PCS		3/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0002119	PMID:33131106	PCS		1/5		HP:0012825	P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0025336	PMID:33131106	PCS		3/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0012171	PMID:33131106	PCS		1/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0000006	PMID:33131106	PCS					I	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0001249	PMID:33131106	PCS		5/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0001337	PMID:33131106	PCS		1/5			P	HPO:probinson[2022-01-23]
OMIM:619561	Developmental and epileptic encephalopathy 97		HP:0003623	PMID:33131106	PCS		1/4			C	HPO:probinson[2022-01-23]
OMIM:607039	Deafness, autosomal recessive 22		HP:0000407	OMIM:607039	TAS					P	HPO:probinson[2013-02-26]
OMIM:607039	Deafness, autosomal recessive 22		HP:0000007	OMIM:607039	TAS					I	HPO:probinson[2013-01-09]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0000132	PMID:34758189;PMID:28134622	PCS		5/6			P	HPO:probinson[2024-02-11];HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0030138	PMID:34758189	PCS		2/3			P	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0011877	PMID:34758189;PMID:28134622	PCS		8/8			P	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0040185	PMID:28134622	PCS		4/5			P	HPO:probinson[2024-02-11];HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0011891	PMID:28134622	PCS		1/2			P	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0011463	PMID:34758189	PCS		3/3			C	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0008320	PMID:34758189	PCS		3/3			P	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0006298	PMID:34758189;PMID:28134622	PCS		3/8			P	HPO:probinson[2024-02-11];HPO:probinson[2024-02-11];HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0000978	PMID:34758189	PCS		3/3			P	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0004846	PMID:28134622	PCS		1/5			P	HPO:probinson[2024-02-11];HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0004406	PMID:34758189	PCS		2/3			P	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0001873	PMID:34758189;PMID:28134622	PCS		4/8			P	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0000006	PMID:28134622	PCS					I	HPO:probinson[2024-02-11]
OMIM:620486	Bleeding disorder, platelet-type, 25		HP:0004866	PMID:34758189	PCS		2/3			P	HPO:probinson[2024-02-11]
OMIM:226200	Enterokinase deficiency		HP:0002014	OMIM:226200	IEA					P	HPO:probinson[2009-02-17]
OMIM:226200	Enterokinase deficiency		HP:0001508	OMIM:226200	TAS					P	HPO:probinson[2009-02-17]
OMIM:226200	Enterokinase deficiency		HP:0007609	OMIM:226200	TAS					P	HPO:probinson[2009-02-17]
OMIM:226200	Enterokinase deficiency		HP:0003075	OMIM:226200	TAS					P	HPO:probinson[2009-02-17]
OMIM:226200	Enterokinase deficiency		HP:0000007	OMIM:226200	TAS					I	HPO:probinson[2009-02-17]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0003621	PMID:34267448	PCS		1/1			C	HPO:probinson[2022-03-27]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0000083	PMID:34267448	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0000790	PMID:34267448;PMID:2227934	PCS		2/2			P	HPO:probinson[2022-03-27];HPO:probinson[2022-05-21]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0034368	PMID:2227934	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0034279	PMID:2227934	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:6000803	PMID:22934314	PCS					P	HPO:probinson[2024-08-03]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0100520	PMID:34267448	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0011463	PMID:2227934	PCS		1/1			C	HPO:probinson[2022-05-21]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0000007	PMID:34267448	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-27]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0000787	PMID:34267448;PMID:2227934	PCS		2/2			P	HPO:probinson[2022-05-21];HPO:probinson[2013-12-15];HPO:probinson[2022-03-27]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0001942	PMID:34267448	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0003259	PMID:34267448	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:614723	Adenine phosphoribosyltransferase deficiency		HP:0002027	PMID:34267448	PCS		1/1			P	HPO:probinson[2022-03-27]
OMIM:191200	Tune deafness		HP:0000365	OMIM:191200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:191200	Tune deafness		HP:0000006	OMIM:191200	IEA					I	HPO:iea[2009-02-17]
OMIM:615429	Deafness, autosomal recessive 88		HP:0000007	PMID:24039609	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2021-09-06]
OMIM:615429	Deafness, autosomal recessive 88		HP:0000410	PMID:24039609	PCS	HP:0003593	6/6			P	HPO:probinson[2021-09-06]
OMIM:158000	Monilethrix		HP:0001596	OMIM:158000	IEA					P	HPO:iea[2009-02-17]
OMIM:158000	Monilethrix		HP:0002299	OMIM:158000	TAS					P	HPO:skoehler[2012-10-17]
OMIM:158000	Monilethrix		HP:0002164	OMIM:158000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:158000	Monilethrix		HP:0032152	OMIM:158000	IEA					P	HPO:skoehler[2019-02-22]
OMIM:158000	Monilethrix		HP:0003828	OMIM:158000	IEA					M	HPO:skoehler[2010-06-19]
OMIM:158000	Monilethrix		HP:0010719	OMIM:158000	TAS					P	HPO:skoehler[2010-06-18]
OMIM:158000	Monilethrix		HP:0003593	OMIM:158000	IEA					C	HPO:skoehler[2010-06-19]
OMIM:158000	Monilethrix		HP:0007468	OMIM:158000	IEA					P	HPO:iea[2009-02-17]
OMIM:158000	Monilethrix		HP:0008404	OMIM:158000	TAS					P	HPO:skoehler[2013-05-03]
OMIM:158000	Monilethrix		HP:0000006	OMIM:158000	TAS					I	HPO:iea[2009-02-17]
OMIM:158000	Monilethrix		HP:0008070	OMIM:158000	TAS					P	HPO:skoehler[2010-06-18]
OMIM:610551	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 1		HP:0005353	PMID:16973841	PCS					P	HPO:probinson[2013-01-09]
OMIM:610551	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 1		HP:0000007	PMID:16973841	PCS					I	HPO:probinson[2013-04-01]
OMIM:610551	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 1		HP:0012302	PMID:16973841	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-07-22]
OMIM:309585	Wilson-Turner syndrome		HP:0000252	PMID:1746601	PCS		2/14			P	HPO:skoehler[2012-12-03];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001344	PMID:1746601	PCS		3/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0000750	PMID:1746601	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001773	PMID:1746601	PCS		3/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0000574	PMID:1746601	PCS		14/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0000771	PMID:1746601	PCS		8/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001761	PMID:1746601	PCS		3/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0025268	PMID:1746601	PCS		6/14			P	HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001263	PMID:1746601	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001182	PMID:1746601	PCS		5/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001419	PMID:25644381	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0000712	PMID:1746601	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001763	PMID:1746601	PCS		4/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0000028	PMID:1746601	PCS		7/14			P	HPO:skoehler[2012-12-03];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001249	PMID:1746601	PCS		14/14			P	HPO:iea[2012-03-01];HPO:probinson[2021-09-28]
OMIM:309585	Wilson-Turner syndrome		HP:0001513	PMID:1746601	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000486	PMID:33565190	PCS		4/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0004322	PMID:33565190	PCS		4/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001134	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001250	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001252	PMID:33565190;PMID:31230721	PCS		16/28			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0011410	PMID:33565190	PCS	HP:0003577	5/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0007082	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000639	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000717	PMID:31230721	PCS		2/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000316	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0008499	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000238	PMID:33565190	PCS		2/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0002415	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001763	PMID:31230721	PCS		2/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001249	PMID:33565190;PMID:31230721	PCS		18/28			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001265	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001382	PMID:33565190;PMID:31230721	PCS		8/28			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0011968	PMID:33565190	PCS	HP:0003623	9/18			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001263	PMID:33565190;PMID:31230721	PCS		24/28			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000407	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000729	PMID:33565190	PCS		3/20			P	HPO:probinson[2021-11-27];HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0002705	PMID:31230721	PCS		3/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000403	PMID:33565190	PCS		5/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0004969	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000322	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000006	PMID:31230721	PCS					I	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000325	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000369	PMID:31230721	PCS		3/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0002003	PMID:31230721	PCS		2/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000540	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001270	PMID:31230721	PCS		6/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0025161	PMID:33565190	PCS		3/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001508	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001629	PMID:33565190	PCS		3/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001947	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0012450	PMID:33565190	PCS		3/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000733	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000736	PMID:31230721	PCS		2/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000256	PMID:33565190;PMID:31230721	PCS		10/26			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0001942	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0006956	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000750	PMID:31230721	PCS		5/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0002573	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0005280	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0012168	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0007099	PMID:33565190	PCS		1/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000348	PMID:31230721	PCS		4/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0000505	PMID:31230721	PCS		1/8			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0025502	PMID:33565190	PCS		6/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0100716	PMID:33565190	PCS		2/20			P	HPO:probinson[2021-11-27];HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0002205	PMID:33565190	PCS		4/20			P	HPO:probinson[2021-11-27]
OMIM:619575	Developmental delay with or without intellectual impairment or behavioral abnormalities		HP:0007018	PMID:33565190;PMID:31230721	PCS		3/28			P	HPO:probinson[2021-11-27]
OMIM:153800	Macular degeneration, age-related, 2		HP:0000608	PMID:9295268	PCS	HP:0003584				P	HP:probinson[2018-07-08]
OMIM:153800	Macular degeneration, age-related, 2		HP:0000006	OMIM:153800	TAS					I	HPO:iea[2009-02-17]
OMIM:618680	Pancreatic cancer, susceptibility to, 5		HP:0002861	PMID:31406347	PCS	HP:0003596				P	HPO:probinson[2020-09-02]
OMIM:618680	Pancreatic cancer, susceptibility to, 5		HP:0006725	PMID:31406347	IEA	HP:0003596				P	HPO:probinson[2020-09-02]
OMIM:618680	Pancreatic cancer, susceptibility to, 5		HP:0000006	PMID:31406347	PCS					I	HPO:probinson[2020-09-02];HPO:probinson[2020-09-02]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000483	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0003676	OMIM:616875	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0002023	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001212	PMID:26942288	PCS		3/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000540	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000188	PMID:26942288	PCS		1/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001332	OMIM:616875	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001272	PMID:26942288	PCS		6/6			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001250	PMID:26942288	PCS		1/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001290	OMIM:616875	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0012444	PMID:26942288	PCS		5/6			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0100704	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000316	PMID:26942288	PCS		1/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000212	PMID:26942288	PCS		4/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0008755	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000278	PMID:26942288	PCS		4/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000512	PMID:26942288	PCS		3/6			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001249	OMIM:616875	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001265	PMID:26942288	PCS		5/6			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0008936	PMID:26942288	PCS		6/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0002059	OMIM:616875	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000750	PMID:26942288	PCS		7/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0002650	PMID:26942288	PCS		5/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0002079	OMIM:616875	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000490	PMID:26942288	PCS		5/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0001263	OMIM:616875;PMID:26942288	PCS		17/17			P	HPO:skoehler[2019-02-22];HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000294	PMID:26942288	PCS		1/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0005484	PMID:26942288	PCS		3/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0007371	PMID:26942288	PCS		6/6			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000649	PMID:26942288	PCS		3/6			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0002509	PMID:26942288	PCS		4/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000007	PMID:26942288	PCS					I	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000648	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000565	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000322	PMID:26942288	PCS		3/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000347	PMID:26942288	PCS		1/7			P	HPO:probinson[2017-06-20]
OMIM:616875	Cerebellar atrophy, visual impairment, and psychomotor retardation		HP:0000545	PMID:26942288	PCS					P	HPO:probinson[2017-06-20]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0030795	PMID:26101329	PCS					P	HPO:probinson[2020-09-03]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0001518	PMID:17855560	PCS	HP:0003577				P	HPO:probinson[2020-09-03]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0003074	PMID:17855560	PCS	HP:0003623				P	HPO:probinson[2020-09-03]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0000007	PMID:26101329	PCS					I	HPO:probinson[2020-09-03]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0100651	PMID:17855560	PCS	HP:0003623				P	HPO:probinson[2020-09-03]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0040217	PMID:17855560	PCS					P	HPO:probinson[2020-09-03]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0000006	PMID:17855560	PCS					I	HPO:probinson[2020-09-03];HPO:probinson[2020-09-03]
OMIM:618858	Diabetes mellitus, permanent neonatal 4		HP:0001953	PMID:17855560	PCS	HP:0003623				P	HPO:probinson[2020-09-03]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0001374	PMID:9732492	PCS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0007759	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0000882	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0004322	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0003298	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0003274	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0000946	PMID:9732492	PCS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0002938	PMID:9732492	PCS					P	HPO:probinson[2017-05-31]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0000568	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0000612	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0004209	PMID:9732492	PCS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0003418	PMID:9732492	PCS					P	HPO:probinson[2017-05-31]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0000894	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0000006	PMID:11146474	PCS					I	HPO:iea[2009-02-17]
OMIM:169550	Pelvis-Shoulder dysplasia		HP:0000588	OMIM:169550	TAS					P	HPO:iea[2009-02-17]
OMIM:621001	Spermatogenic failure 96		HP:0003251	PMID:35285020;PMID:34392356	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:621001	Spermatogenic failure 96		HP:0011462	PMID:35285020;PMID:34392356	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:621001	Spermatogenic failure 96		HP:0030087	PMID:35285020	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:621001	Spermatogenic failure 96		HP:0000007	PMID:34392356	PCS					I	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:621001	Spermatogenic failure 96		HP:0011961	PMID:35285020;PMID:34392356	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:621001	Spermatogenic failure 96		HP:0031039	PMID:35285020	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:621001	Spermatogenic failure 96		HP:0000028	PMID:35285020	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:621001	Spermatogenic failure 96		HP:0030338	PMID:35285020	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-12-24]
OMIM:600971	Deafness, autosomal recessive 6		HP:0003577	PMID:12145746	PCS					C	HPO:probinson[2024-03-16]
OMIM:600971	Deafness, autosomal recessive 6		HP:0000365	PMID:12145746	PCS	HP:0003577	15/15			P	HPO:skoehler[2013-01-11];HPO:probinson[2024-03-16]
OMIM:600971	Deafness, autosomal recessive 6		HP:0000007	PMID:12145746	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2024-03-16]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003554	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003577	OMIM:605809	IEA					C	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0000486	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0002882	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003473	OMIM:605809	TAS					P	HPO:probinson[2012-04-12]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003198	OMIM:605809	IEA					P	HPO:skoehler[2018-10-08]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003397	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0001290	OMIM:605809	TAS					P	HPO:probinson[2012-04-12]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003690	OMIM:605809	TAS					P	HPO:skoehler[2015-05-31]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0008872	OMIM:605809	TAS					P	HPO:probinson[2012-04-12]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0000597	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003402	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003403	PMID:7531341	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003623	PMID:7531341	PCS		1/1			C	HPO:probinson[2023-02-18]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0002872	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0002015	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0003388	OMIM:605809	TAS					P	HPO:skoehler[2015-05-31]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0001283	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0002098	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0002033	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0000508	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0000007	PMID:7531341	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-18]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0002747	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0000006	OMIM:605809	TAS					I	HPO:skoehler[2015-12-30]
OMIM:605809	Myasthenic syndrome, congenital, 4A, slow-channel		HP:0001612	OMIM:605809	IEA					P	HPO:iea[2009-02-17]
OMIM:600965	Deafness, autosomal dominant 6		HP:0003621	PMID:11709538	PCS					C	HPO:probinson[2022-04-12]
OMIM:600965	Deafness, autosomal dominant 6		HP:0000408	PMID:11709538	PCS					P	HPO:probinson[2012-03-30];HPO:probinson[2022-04-12]
OMIM:600965	Deafness, autosomal dominant 6		HP:0008573	PMID:11709538	PCS					P	HPO:probinson[2012-03-30];HPO:probinson[2022-04-12]
OMIM:600965	Deafness, autosomal dominant 6		HP:0000006	PMID:11709538	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-12]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0008619	PMID:25256757	PCS		4/7			P	HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000053	PMID:10677307	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000581	PMID:10677307	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0045025	PMID:25256757	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000280	PMID:25256757	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0001419	PMID:25256757	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000629	PMID:10677307	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000414	PMID:25256757	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000400	PMID:25256757	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000179	PMID:25256757	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0000336	PMID:10677307	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:300238	Intellectual developmental disorder, X-linked syndromic, Shashi type		HP:0001513	PMID:25256757	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-28]
OMIM:609941	Deafness, autosomal recessive 51		HP:0000407	PMID:16158433	PCS	HP:0003593				P	HPO:probinson[2009-02-17];HP:probinson[2019-01-20]
OMIM:609941	Deafness, autosomal recessive 51		HP:0000007	PMID:16158433	PCS					I	HPO:probinson[2009-02-17];HP:probinson[2019-01-20]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0003202	PMID:24482476	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0001771	PMID:24482476	PCS		2/4			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000252	PMID:34585293	PCS		1/2			P	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0002650	PMID:24482476	PCS		1/4			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000750	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0031936	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0011968	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0001260	PMID:24482476	PCS		0/4			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0003474	PMID:24482476	PCS		0/3			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0001263	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0003593	PMID:24482476	PCS		4/4			C	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0002380	PMID:24482476	PCS		0/3			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0001270	PMID:24482476	PCS		4/4			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0011448	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000407	PMID:34585293	PCS		1/2			P	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000316	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000007	PMID:24482476	PCS					I	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000218	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0001257	PMID:34585293;PMID:24482476	PCS		6/6			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0001510	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000369	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0000347	PMID:34585293	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620323	Spastic paraplegia 70, autosomal recessive		HP:0001347	PMID:24482476	PCS		3/3			P	HPO:probinson[2023-07-09]
OMIM:616849	Brachydactyly, type A1, D		HP:0002311	PMID:25758993	PCS					P	HPO:probinson[2017-06-23]
OMIM:616849	Brachydactyly, type A1, D		HP:0001760	PMID:25758993	PCS		0/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0003577	PMID:25758993	PCS		2/2			C	HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0000750	PMID:25758993	PCS		1/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0009650	PMID:25758993	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0010241	PMID:25758993	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0004220	PMID:25758993	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0009566	PMID:25758993	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0009568	PMID:25758993	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0004209	PMID:25758993	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:616849	Brachydactyly, type A1, D		HP:0000006	PMID:25758993	PCS					I	HPO:probinson[2017-06-23]
OMIM:616849	Brachydactyly, type A1, D		HP:0009638	PMID:25758993	PCS		2/2			P	HPO:probinson[2017-06-23];HPO:probinson[2022-03-26]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0001265	OMIM:606482	IEA					P	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0003621	OMIM:606482	IEA					C	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0001761	OMIM:606482	IEA					P	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0003693	OMIM:606482	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0003383	OMIM:606482	IEA					P	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0001284	OMIM:606482	IEA					P	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0002460	OMIM:606482	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0003481	OMIM:606482	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0003380	OMIM:606482	IEA					P	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0040078	OMIM:606482	TAS					P	HPO:skoehler[2014-11-26]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0002936	OMIM:606482	IEA					P	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0000006	OMIM:606482	IEA					I	HPO:iea[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0007107	OMIM:606482	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:606482	Charcot-Marie-Tooth disease, dominant intermediate B		HP:0000764	OMIM:606482	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0005576	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0004322	PMID:2918547	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001370	OMIM:607944	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0005374	OMIM:607944	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0100255	PMID:26951490	PCS		24/25			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0011463	PMID:2918547	PCS		2/4			C	HPO:probinson[2020-10-31];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002938	PMID:2918547	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001888	PMID:26951490	PCS		6/13			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002657	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0007526	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002751	OMIM:607944	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001386	PMID:2918547	PCS		3/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001264	OMIM:607944	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0005387	OMIM:607944	TAS					P	HPO:probinson[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001263	PMID:26951490	PCS		7/25			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0011800	PMID:2918547	PCS		2/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000926	PMID:2918547;PMID:26951490	PCS		28/29			P	HPO:probinson[2020-10-31];HPO:iea[2009-02-17];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000403	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000007	PMID:2918547	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001973	PMID:26951490	PCS		12/26			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001257	PMID:26951490	PCS		11/25			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000369	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001034	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002960	PMID:26951490	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0003577	PMID:2918547	PCS		2/4			C	HPO:probinson[2020-10-31];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0003016	PMID:2918547	PCS		4/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001552	PMID:2918547	PCS		2/4			P	HPO:probinson[2020-10-31];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000460	OMIM:607944	TAS					P	HPO:probinson[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000262	PMID:2918547	PCS		1/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0003493	PMID:26951490	PCS		21/22			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000979	OMIM:607944	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0100866	PMID:2918547	PCS		3/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002716	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002958	PMID:26951490	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0004979	OMIM:607944	TAS					P	HPO:probinson[2012-05-26]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002514	PMID:26951490	PCS		9/14			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002478	OMIM:607944	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001045	OMIM:607944	IEA					P	HPO:skoehler[2010-06-20]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0005403	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0003301	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0003621	OMIM:607944	IEA					C	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002650	PMID:2918547	PCS		1/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002694	PMID:2918547	PCS		1/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0003025	OMIM:607944	TAS					P	HPO:probinson[2012-05-26]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0030320	PMID:2918547	PCS		2/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0030880	PMID:26951490	PCS		6/51			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0005681	OMIM:607944	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002090	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002091	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0011108	OMIM:607944	TAS					P	HPO:probinson[2012-05-26]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0000821	OMIM:607944	IEA					P	HPO:iea[2009-02-17]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002725	PMID:26951490	PCS		7/26			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002205	PMID:26951490	PCS		3/25			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0002007	PMID:2918547	PCS		1/4			P	HPO:probinson[2020-10-31]
OMIM:607944	Spondyloenchondrodysplasia with immune dysregulation		HP:0001875	PMID:26951490	PCS		3/8			P	HPO:probinson[2020-10-31]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000121	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002069	PMID:23636107	PCS		1/4			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000164	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000486	PMID:23636107	PCS		4/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0004443	PMID:23636107	PCS		1/2			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001250	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001252	PMID:23636107	PCS		4/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0003196	OMIM:615398	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001251	OMIM:615398	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0003593	OMIM:615398	TAS					C	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001290	OMIM:615398	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0032794	PMID:23636107	PCS		2/4			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0010841	PMID:23636107	PCS		3/4			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000639	PMID:23636107	PCS		4/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001723	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001643	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001249	PMID:23636107	PCS		4/4			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000496	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0003487	OMIM:615398	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002750	PMID:23636107	PCS		4/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001263	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002150	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0011448	OMIM:615398	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0011330	PMID:23636107	PCS		1/2			P	HPO:probinson[2022-10-11];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000767	PMID:23636107	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000007	PMID:23636107	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000565	OMIM:615398	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000248	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000369	OMIM:615398	IEA					P	HPO:skoehler[2019-04-18]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000341	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0003577	PMID:23636107	PCS		4/4			C	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000343	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000463	OMIM:615398	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002002	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000540	PMID:23636107	PCS		4/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001272	PMID:23636107	PCS		2/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002121	PMID:23636107	PCS		1/4			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000939	OMIM:615398	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0100704	PMID:23636107	PCS		4/4			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000938	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002714	OMIM:615398	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000218	OMIM:615398	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000256	OMIM:615398	TAS				HP:0012825	P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002059	PMID:23636107	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001520	OMIM:615398	TAS				HP:0012825	P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002650	PMID:23636107	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0001321	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0002376	OMIM:615398	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0003022	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000194	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000072	PMID:23636107	PCS		3/4			P	HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0003186	PMID:23636107	PCS		2/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000071	OMIM:615398	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0005280	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000107	PMID:23636107	PCS		1/4			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-10-11]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000348	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3		HP:0000505	OMIM:615398	TAS					P	HPO:skoehler[2013-10-06]
OMIM:216300	Cleft palate, deafness, and oligodontia		HP:0010109	OMIM:216300	IEA					P	HPO:iea[2009-02-17]
OMIM:216300	Cleft palate, deafness, and oligodontia		HP:0000185	OMIM:216300	IEA					P	HPO:iea[2009-02-17]
OMIM:216300	Cleft palate, deafness, and oligodontia		HP:0000007	OMIM:216300	IEA					I	HPO:iea[2009-02-17]
OMIM:216300	Cleft palate, deafness, and oligodontia		HP:0001852	OMIM:216300	IEA					P	HPO:iea[2009-02-17]
OMIM:216300	Cleft palate, deafness, and oligodontia		HP:0008513	OMIM:216300	IEA					P	HPO:iea[2009-02-17]
OMIM:216300	Cleft palate, deafness, and oligodontia		HP:0012225	OMIM:216300	TAS					P	HPO:probinson[2013-03-30]
OMIM:216300	Cleft palate, deafness, and oligodontia		HP:0006349	OMIM:216300	TAS					P	HPO:probinson[2009-02-17]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000486	PMID:36724785	PCS		6/11			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0004322	PMID:36724785	PCS		8/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0001772	PMID:36724785	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0001250	PMID:36724785	PCS		4/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002066	PMID:36724785	PCS		3/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0001252	PMID:36724785	PCS		5/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0003593	PMID:36724785	PCS					C	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002061	PMID:36724785	PCS		4/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0007380	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0100704	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000319	PMID:36724785	PCS		3/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002515	PMID:36724785	PCS		2/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002812	PMID:36724785	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002216	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000752	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0001249	PMID:36724785	PCS		9/9			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000252	PMID:36724785	PCS		9/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000076	PMID:36724785	PCS		2/7			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000750	PMID:36724785	PCS		11/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002650	PMID:36724785	PCS		5/10			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0031936	PMID:36724785	PCS		9/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002970	PMID:36724785	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000771	PMID:36724785	PCS		2/6			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0001263	PMID:36724785	PCS		11/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002072	PMID:36724785	PCS		6/22			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0100710	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0034373	PMID:36724785	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000749	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000007	PMID:36724785	PCS					I	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0002307	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000565	PMID:36724785	PCS		2/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000369	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000742	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:620445	Neurodevelopmental disorder with microcephaly and movement abnormalities		HP:0000687	PMID:36724785	PCS		1/11			P	HPO:probinson[2024-03-02]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0000275	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0001792	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0000750	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0000276	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0000639	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0001419	PMID:12070254	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0000689	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0000322	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0001249	PMID:14735593;PMID:12070254	PCS		6/6			P	HPO:probinson[2021-09-28]
OMIM:300210	Intellectual developmental disorder, X-linked 58		HP:0000545	PMID:14735593	PCS		1/1			P	HPO:probinson[2021-09-28]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002300	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0003596	PMID:16041373	PCS					C	HPO:probinson[2021-02-19]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002442	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0001332	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002145	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002120	OMIM:600795	TAS					P	HPO:probinson[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002063	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000020	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000719	OMIM:600795	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000718	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000734	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000711	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000733	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000757	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000751	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000710	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0001347	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0003487	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0001288	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002354	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002310	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002371	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002529	OMIM:600795	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000741	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000006	PMID:16041373	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-19]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0000743	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0002446	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:600795	Frontotemporal dementia and/or amytrophic lateral sclerosis 7		HP:0001336	OMIM:600795	IEA					P	HPO:iea[2009-02-17]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0002069	PMID:36823193	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000286	PMID:36823193	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0002267	PMID:36823193	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000486	PMID:36823193	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0002066	PMID:36823193	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0003155	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0012707	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001251	PMID:36823193	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0003593	PMID:36823193	PCS		1/7			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0010763	PMID:36823193	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0012389	PMID:36823193	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0033725	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000639	PMID:36823193	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0011463	PMID:36823193	PCS		5/7			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001324	PMID:36823193	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000597	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001249	PMID:36823193	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0003348	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0003623	PMID:36823193	PCS		1/7			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000572	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000252	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0003200	PMID:36823193	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0011968	PMID:36823193	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0002151	PMID:36823193	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001263	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0011923	PMID:36823193	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0034353	PMID:36823193	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0025405	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000648	PMID:36823193	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000369	PMID:36823193	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000006	PMID:36823193	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001336	PMID:36823193	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0004887	PMID:36823193	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001272	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0012847	PMID:36823193	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0007663	PMID:36823193	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001943	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0003648	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0008358	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0007305	PMID:36823193	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0003403	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0008936	PMID:36823193	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000750	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0001288	PMID:36823193	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0002013	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0002171	PMID:36823193	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000508	PMID:36823193	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0000426	PMID:36823193	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0009830	PMID:36823193	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620451	Combined oxidative phosphorylation deficiency 58		HP:0008347	PMID:36823193	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001371	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001250	PMID:7637805	PCS		9/16			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001252	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001251	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0002361	PMID:7637805	PCS		15/16			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001290	OMIM:256730	TAS					P	HPO:skoehler[2017-07-13]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000716	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000738	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000737	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000618	OMIM:256730	TAS	HP:0011463				P	HPO:probinson[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001922	PMID:7637805	PCS		0/12			P	HPO:probinson[2023-02-22]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001249	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000654	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000253	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000550	OMIM:256730	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0002059	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0003621	PMID:7637805	PCS		16/16			C	HPO:probinson[2023-02-22]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0002353	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001263	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0002074	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0002371	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0005484	OMIM:256730	TAS					P	HPO:probinson[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:6000783	PMID:9535296	PCS		5/5			P	HPO:probinson[2024-06-29]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000529	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001939	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000608	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000007	PMID:7637805	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000546	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0000648	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0003657	PMID:7637805	PCS		16/16			P	HPO:probinson[2023-02-22]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001257	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:256730	Ceroid lipofuscinosis, neuronal, 1		HP:0001336	OMIM:256730	IEA					P	HPO:iea[2009-02-17]
OMIM:125000	Deafness, unilateral		HP:0009900	OMIM:125000	TAS					P	HPO:probinson[2013-03-10]
OMIM:125000	Deafness, unilateral		HP:0000006	OMIM:125000	TAS					I	HPO:probinson[2009-02-17]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0001133	PMID:20625056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0003621	PMID:20625056	PCS		9/24			C	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0001099	PMID:20625056	PCS		15/25			P	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0000662	PMID:20625056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0000580	PMID:20625056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0011003	PMID:20625056	PCS		11/19			P	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0030529	PMID:20625056	PCS		4/25			P	HPO:probinson[2022-03-15];HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0011504	PMID:20625056	PCS		7/25			P	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0000518	OMIM:312600	IEA					P	HPO:iea[2009-02-17]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0011463	PMID:20625056	PCS		11/24			C	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0011462	PMID:20625056	PCS		4/24			C	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0007761	PMID:20625056	PCS		1/25			P	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0001417	PMID:9697692	PCS					I	HPO:skoehler[2015-02-11];HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0000603	PMID:20625056	PCS		13/25			P	HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0000510	PMID:20625056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0200065	PMID:20625056	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:312600	Retinitis pigmentosa 2, X-linked		HP:0000545	PMID:20625056	PCS		19/19			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-15]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0000175	OMIM:602196	IEA					P	HPO:skoehler[2010-06-20]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0000772	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0001382	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0001252	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0000767	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0001290	OMIM:602196	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0001965	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0006631	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0000201	OMIM:602196	TAS					P	HPO:probinson[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0000465	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0000006	OMIM:602196	IEA					I	HPO:iea[2009-02-17]
OMIM:602196	Pierre Robin sequence with pectus excavatum and rib and scapular anomalies		HP:0000347	OMIM:602196	IEA					P	HPO:iea[2009-02-17]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001276	OMIM:613925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0002344	PMID:21419380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0002059	PMID:21419380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0003577	PMID:21419380	PCS		3/10			C	HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0002015	PMID:21419380	PCS		8/20			P	HPO:probinson[2022-10-03];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0000750	PMID:21419380	PCS		4/20			P	HPO:probinson[2022-10-03];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001355	PMID:21419380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001272	PMID:21419380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001250	PMID:21419380	PCS		8/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001260	PMID:21419380	PCS		7/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001251	PMID:21419380	PCS		7/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0003593	PMID:21419380	PCS		3/10			C	HPO:probinson[2022-10-03];HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0002061	PMID:21419380	PCS		7/10			P	HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001270	PMID:21419380	PCS		4/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0011463	PMID:21419380	PCS		4/10			C	HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0007341	PMID:21419380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0000007	PMID:21419380	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0002119	OMIM:613925	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0007204	PMID:21419380	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0000256	PMID:21419380	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001268	PMID:21419380	PCS		9/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-03]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0001249	PMID:21419380	PCS		5/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0003677	PMID:21419380	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613925	Megalencephalic leukoencephalopathy with subcortical cysts 2A		HP:0006986	PMID:21419380	PCS		4/10			P	HPO:probinson[2022-10-03]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001331	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0002983	PMID:27599773	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000343	PMID:27599773	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001377	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0004322	PMID:31325655;PMID:27599773;PMID:31705726	PCS		4/4			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000463	PMID:27599773;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001156	PMID:27599773;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000540	PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0003691	PMID:31325655	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001373	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001252	PMID:31705726	PCS	HP:0003593	2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0005274	PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0033102	PMID:31325655;PMID:27599773	PCS		2/2			P	HPO:probinson[2020-10-12]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001270	PMID:31705726	PCS		2/2		HP:0012825	P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0006094	PMID:27599773	PCS	HP:0011463	1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001629	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0007165	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000954	PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0003307	PMID:31325655;PMID:27599773;PMID:31705726	PCS		3/4			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0002119	PMID:31705726	PCS		2/2		HP:0012825	P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0002857	PMID:31325655	PCS		1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001643	PMID:31705726	PCS	HP:0003577	1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000311	PMID:27599773	PCS		1/1			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001763	PMID:31325655;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000256	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000494	PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0002650	PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001382	PMID:31325655;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0003066	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0004691	PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0011800	PMID:27599773;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0005280	PMID:27599773;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0003180	PMID:31325655;PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0005180	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0040022	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000308	PMID:27599773;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0010880	PMID:31705726	IEA	HP:0030674	1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000767	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000007	PMID:27599773	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0003417	PMID:27599773;PMID:31705726	PCS		3/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0005616	PMID:27599773	PCS	HP:0011463	1/1			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0003316	PMID:27599773;PMID:31705726	PCS		2/3			P	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0002007	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0000444	PMID:31705726	PCS		2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0007018	PMID:31705726	PCS		2/2		HP:0012825	P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001631	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0002643	PMID:31705726	PCS	HP:0003623	2/2			P	HPO:probinson[2020-08-13]
OMIM:618870	Skeletal dysplasia, mild, with joint laxity and advanced bone age		HP:0001655	PMID:31705726	PCS		1/2			P	HPO:probinson[2020-08-13]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0002069	PMID:24928908	PCS		6/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0003621	PMID:24928908	PCS		3/7			C	HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0025709	PMID:24928908	PCS		2/7			C	HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0002123	PMID:24928908	PCS		3/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0002373	PMID:24928908	PCS		0/8			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0001250	PMID:24928908	PCS		9/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0002121	PMID:24928908	PCS		4/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0011463	PMID:24928908	PCS		1/7			C	HPO:probinson[2023-01-21]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0003829	OMIM:616685	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616685	Epilepsy, idiopathic generalized, susceptibility to, 14		HP:0000006	PMID:24928908	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-01-21]
OMIM:602197	Cerebellar degeneration-related autoantigen 3		HP:0001317	OMIM:602197	IEA					P	HPO:skoehler[2013-01-09]
OMIM:605820	Nonaka myopathy		HP:0003236	PMID:12177386	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-06-11]
OMIM:605820	Nonaka myopathy		HP:0001288	OMIM:605820	IEA					P	HPO:iea[2009-02-17]
OMIM:605820	Nonaka myopathy		HP:0009053	PMID:12177386	PCS	HP:0003581	6/9			P	HP:probinson[2019-06-11]
OMIM:605820	Nonaka myopathy		HP:0003693	OMIM:605820	IEA					P	HPO:iea[2009-02-17]
OMIM:605820	Nonaka myopathy		HP:0003581	OMIM:605820	IEA					C	HPO:iea[2009-02-17]
OMIM:605820	Nonaka myopathy		HP:0002460	OMIM:605820	IEA					P	HPO:iea[2009-02-17]
OMIM:605820	Nonaka myopathy		HP:0003791	OMIM:605820	IEA					P	HPO:iea[2009-02-17]
OMIM:605820	Nonaka myopathy		HP:0000007	PMID:12177386	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-06-11]
OMIM:605820	Nonaka myopathy		HP:0003805	PMID:12177386	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-06-11]
OMIM:605820	Nonaka myopathy		HP:0003458	OMIM:605820	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001311	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001310	OMIM:256731	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001272	PMID:15728307	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0002120	PMID:15728307	PCS		2/2			P	HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001250	PMID:15728307	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001251	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0000639	OMIM:256731	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001922	PMID:15728307	PCS		0/2			P	HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0003208	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001249	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0003226	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0003205	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0200085	PMID:15728307	PCS		2/2			P	HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0002333	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0002312	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0003621	PMID:15728307	PCS		2/2			C	HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0002376	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001260	OMIM:256731	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0002074	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0002075	OMIM:256731	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0000529	PMID:15728307	PCS	HP:0003621	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0000007	PMID:9662406	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0000546	OMIM:256731	IEA					P	HPO:iea[2009-02-17]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0002505	PMID:15728307	PCS		2/2			P	HPO:probinson[2023-02-07]
OMIM:256731	Ceroid lipofuscinosis, neuronal, 5		HP:0001336	PMID:15728307	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-07]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0004322	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0012745	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0010296	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0012471	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002938	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000637	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002019	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0006237	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000358	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000995	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002553	PMID:35904126	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000252	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000098	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000494	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000490	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0004691	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0032521	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001060	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0100023	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0011094	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000403	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002944	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0004209	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002307	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000405	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000400	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000369	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000006	PMID:35904126	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000582	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002002	PMID:35904126	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000463	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002000	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000185	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0008872	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000218	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0006610	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000179	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0006855	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001320	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000750	PMID:35904126	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0003189	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002650	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000232	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002373	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000072	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0011225	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002808	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0004942	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000742	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001377	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001250	PMID:35904126	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002186	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001371	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001252	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0010806	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0011856	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0100962	PMID:35904126	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000957	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000319	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000718	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0011462	PMID:35904126	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000717	PMID:35904126	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0003307	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0025336	PMID:35904126	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000278	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001763	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001249	PMID:35904126	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000574	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002474	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000331	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0002750	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001382	PMID:35904126	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0012412	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0006380	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000729	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000448	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0007598	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000444	PMID:35904126	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001257	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000322	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000289	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000445	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000687	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000540	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000023	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0040080	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0012771	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0008551	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0001863	PMID:35904126	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000774	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000431	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0031936	PMID:35904126	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000430	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0045025	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0034373	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000426	PMID:35904126	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0030051	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000664	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620450	Intellectual developmental disorder, autosomal dominant 73		HP:0000028	PMID:35904126	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:171450	Phlebectasia of lips		HP:0000006	OMIM:171450	IEA					I	HPO:iea[2009-02-17]
OMIM:171450	Phlebectasia of lips		HP:0000159	OMIM:171450	IEA					P	HPO:iea[2012-07-24]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0002751	PMID:24027061	PCS					P	HPO:skoehler[2015-12-30]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0003202	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0000365	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0001288	PMID:24027061	PCS					P	HPO:skoehler[2015-12-30]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0001332	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0003388	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0002151	PMID:24027061	PCS					P	HPO:skoehler[2015-12-30]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0001251	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0001284	OMIM:616684	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0011096	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0000407	PMID:24027061	PCS				HP:0012825	P	HPO:skoehler[2015-12-30]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0003828	OMIM:616684	TAS					M	HPO:skoehler[2017-07-13]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0009830	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0000007	PMID:24027061	PCS					I	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0000666	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0003677	OMIM:616684	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616684	Charcot-Marie-Tooth disease, type 4K		HP:0003447	PMID:24027061	PCS					P	HPO:probinson[2017-06-18]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0002014	PMID:23733340	PCS		1/1			P	HPO:skoehler[2013-09-30]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0003596	PMID:23733340	PCS		1/1			C	HPO:probinson[2023-06-05]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0001442	PMID:23733340	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-06-05]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0002829	PMID:23733340	PCS		1/1			P	HPO:skoehler[2013-09-30]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0004818	PMID:23733340	PCS		1/1			P	HPO:skoehler[2015-01-27]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0001878	PMID:23733340	PCS		1/1			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-06-05]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0002094	PMID:23733340	PCS		1/1			P	HPO:skoehler[2013-09-30]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0002315	PMID:23733340	PCS		1/1			P	HPO:skoehler[2013-09-30]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0012378	PMID:23733340	PCS		1/1			P	HPO:skoehler[2013-10-22]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0002027	PMID:23733340	PCS		1/1			P	HPO:skoehler[2013-09-30]
OMIM:615399	Paroxysmal nocturnal hemoglobinuria 2		HP:0000006	PMID:23733340	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-06-05]
OMIM:613930	Alopecia-intellectual disability syndrome 3		HP:0002289	OMIM:613930	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613930	Alopecia-intellectual disability syndrome 3		HP:0003577	OMIM:613930	TAS					C	HPO:skoehler[2012-10-17]
OMIM:613930	Alopecia-intellectual disability syndrome 3		HP:0000007	OMIM:613930	TAS					I	HPO:skoehler[2012-10-17]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003378	OMIM:606483	TAS					P	HPO:probinson[2009-02-17]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001265	PMID:32937143	PCS		1/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003445	PMID:32937143	PCS		6/7			P	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003596	PMID:32937143	PCS		4/7			C	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003376	OMIM:606483	IEA					P	HPO:iea[2009-02-17]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001761	PMID:32937143	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001288	PMID:32937143	PCS		4/7			P	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003693	OMIM:606483	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001260	PMID:32937143	PCS		1/7		HP:0012825	P	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003394	PMID:32937143	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003383	OMIM:606483	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001284	PMID:32937143	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0002460	PMID:32937143	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003481	OMIM:606483	IEA					P	HPO:iea[2009-02-17]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0003393	PMID:32937143	PCS		1/7			P	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001270	PMID:32937143	PCS		1/7			P	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0011463	PMID:32937143	PCS		1/7			C	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0011462	PMID:32937143	PCS		2/7			C	HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0009027	PMID:32937143	PCS		5/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0002936	PMID:32937143	PCS		3/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0000006	PMID:32937143	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0007107	OMIM:606483	TAS					P	HPO:skoehler[2009-02-17]
OMIM:606483	Charcot-Marie-Tooth disease, dominant intermediate A		HP:0001765	PMID:32937143	PCS		1/7			P	HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0003621	PMID:15161766	PCS		6/10			C	HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0034384	PMID:15161766	PCS		10/10			P	HPO:probinson[2022-10-07]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0008283	PMID:15161766	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0000825	PMID:15161766	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0011463	PMID:15161766	PCS		1/10			C	HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0002173	PMID:15161766	PCS		5/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0011462	PMID:15161766	PCS		3/10			C	HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0000006	PMID:15161766	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:609968	Hyperinsulinemic hypoglycemia, familial, 5		HP:0001325	PMID:15161766	PCS		8/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:620322	C1q deficiency 3		HP:0007417	PMID:8630118	PCS		2/2			P	HPO:probinson[2023-06-27];HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0003621	PMID:21654842	PCS		1/1			C	HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0011463	PMID:8630118	PCS		1/2			C	HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0007274	PMID:21654842	PCS		1/1			P	HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0003493	PMID:8630118	PCS		2/2			P	HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0000007	PMID:8630118	PCS					I	HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0034601	PMID:21654842;PMID:8630118	PCS		3/3			P	HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0032435	PMID:8630118	PCS		1/2			P	HPO:probinson[2023-06-27]
OMIM:620322	C1q deficiency 3		HP:0003623	PMID:8630118	PCS		1/2			C	HPO:probinson[2023-06-27]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0000286	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001572	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001773	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001344	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001250	OMIM:300577	IEA					P	HPO:skoehler[2015-07-28]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0006829	OMIM:300577	IEA	HP:0003593				P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001263	OMIM:300577	IEA		20/20			P	HPO:skoehler[2013-01-09];HPO:skoehler[2019-02-22]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0003196	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0002162	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001999	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001417	OMIM:300577	IEA					I	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0009237	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0000218	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0002967	OMIM:300577	TAS					P	HPO:skoehler[2015-11-15];HP:probinson[2019-01-04]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0030084	OMIM:300577	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0200055	OMIM:300577	IEA					P	HPO:skoehler[2013-01-09]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001423	OMIM:300577	TAS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:300577	Intellectual developmental disorder, X-linked 91		HP:0001513	OMIM:300577	IEA	HP:0003593				P	HPO:skoehler[2013-01-09]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0001761	OMIM:600794	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003693	OMIM:600794	TAS					P	HPO:probinson[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003484	OMIM:600794	IEA					P	HPO:iea[2012-03-15]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0002460	OMIM:600794	TAS		20/20			P	HPO:probinson[2012-07-16];HPO:iea[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003392	OMIM:600794	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003393	OMIM:600794	IEA					P	HPO:iea[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0011462	PMID:12690580	PCS					C	HPO:probinson[2022-09-04]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0009830	OMIM:600794	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003426	OMIM:600794	IEA					P	HPO:iea[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0001763	OMIM:600794	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003427	OMIM:600794	IEA					P	HPO:iea[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0009129	OMIM:600794	IEA					P	HPO:iea[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0000006	PMID:12690580	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003435	OMIM:600794	IEA					P	HPO:iea[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0003677	OMIM:600794	IEA					C	HPO:iea[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0001765	OMIM:600794	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:600794	Neuronopathy, distal hereditary motor, type VA		HP:0001347	OMIM:600794	IEA		HP:0040283			P	HPO:probinson[2012-03-15]
OMIM:620444	Craniofacial microsomia 2		HP:0003577	PMID:36260083	PCS		10/10			C	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:5201016	PMID:36260083	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0011266	PMID:36260083	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0000193	PMID:36260083	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0010609	PMID:36260083	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0008551	PMID:36260083	PCS		10/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0011267	PMID:36260083	PCS		8/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0020223	PMID:36260083	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0008569	PMID:36260083	PCS		1/10			P	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0000006	PMID:36260083	PCS					I	HPO:probinson[2024-03-02]
OMIM:620444	Craniofacial microsomia 2		HP:0000347	PMID:36260083	PCS		3/10			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:300211	Episodic muscle weakness, X-linked		HP:0001417	OMIM:300211	IEA					I	HPO:skoehler[2013-01-11]
OMIM:300211	Episodic muscle weakness, X-linked		HP:0001324	OMIM:300211	IEA		HP:0040280			P	HPO:skoehler[2013-01-09]
OMIM:612390	Pontocerebellar hypoplasia, type 2C		HP:0001320	PMID:18711368	PCS					P	HPO:probinson[2013-04-14]
OMIM:612390	Pontocerebellar hypoplasia, type 2C		HP:0000252	PMID:18711368	PCS					P	HPO:probinson[2013-04-14]
OMIM:612390	Pontocerebellar hypoplasia, type 2C		HP:0001332	PMID:18711368	PCS					P	HPO:probinson[2013-04-14]
OMIM:612390	Pontocerebellar hypoplasia, type 2C		HP:0100307	PMID:18711368	PCS					P	HPO:probinson[2013-04-14]
OMIM:612390	Pontocerebellar hypoplasia, type 2C		HP:0002072	PMID:18711368	PCS					P	HPO:probinson[2013-04-14]
OMIM:612390	Pontocerebellar hypoplasia, type 2C		HP:0000007	PMID:18711368	PCS					I	HPO:probinson[2013-04-14]
OMIM:612390	Pontocerebellar hypoplasia, type 2C		HP:0000505	PMID:18711368	PCS					P	HPO:probinson[2013-04-14]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0002908	OMIM:243300	TAS					P	HPO:probinson[2009-02-17]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0000365	PMID:19478059	PCS					P	HPO:probinson[2016-07-03]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0001046	OMIM:243300	TAS					P	HPO:probinson[2012-07-24]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0002240	OMIM:243300	TAS					P	HPO:probinson[2009-02-17]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0000007	OMIM:243300	TAS					I	HPO:probinson[2009-02-17]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0000989	OMIM:243300	TAS					P	HPO:probinson[2009-02-17]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0006575	OMIM:243300	TAS					P	HPO:probinson[2009-02-17]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0012202	OMIM:243300	TAS					P	HPO:probinson[2016-07-03]
OMIM:243300	Cholestasis, benign recurrent intrahepatic 1		HP:0001733	OMIM:243300	TAS					P	HPO:probinson[2009-02-17]
OMIM:169545	Pelvic lipomatosis with crossed renal ectopia		HP:0000086	OMIM:169545	IEA					P	HPO:iea[2009-02-17]
OMIM:169545	Pelvic lipomatosis with crossed renal ectopia		HP:0034009	OMIM:169545	TAS					P	HPO:probinson[2021-10-03]
OMIM:169545	Pelvic lipomatosis with crossed renal ectopia		HP:0000006	OMIM:169545	IEA					I	HPO:iea[2009-02-17]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0025066	PMID:17485548	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0001394	OMIM:616860	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0002240	OMIM:616860	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0003281	PMID:25342667	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0012132	PMID:25342667	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0011273	PMID:25342667	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0002908	PMID:17485548	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0012465	PMID:25342667	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0001903	PMID:25342667	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0032231	OMIM:616860	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0000007	PMID:25342667	PCS					I	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0001433	PMID:25342667	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0005978	PMID:25342667	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0002910	PMID:17485548	PCS					P	HPO:probinson[2017-06-18]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0001744	OMIM:616860	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616860	Anemia, sideroblastic, 3, pyridoxine-refractory		HP:0000952	OMIM:616860	TAS					P	HPO:skoehler[2017-07-13]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0002257	PMID:25048963	PCS					P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0002110	PMID:25048963	PCS		9/9			P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0032341	PMID:25048963	PCS					P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0033036	PMID:25048963	PCS		7/7			P	HPO:probinson[2020-09-13]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0000007	PMID:25048963	PCS					I	HPO:probinson[2020-06-28];HPO:probinson[2021-02-25]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0100582	PMID:25048963	PCS					P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0006510	PMID:25048963	PCS					P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0002093	PMID:25048963	PCS		2/9			P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0002090	PMID:25048963	PCS		9/9			P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0011108	PMID:25048963	PCS		11/13			P	HPO:probinson[2020-06-28]
OMIM:618695	Ciliary dyskinesia, primary, 42		HP:0003623	PMID:25048963	PCS					C	HPO:probinson[2020-06-28]
OMIM:310980	OMPHALOCELE		HP:0003577	OMIM:310980	TAS					C	HPO:probinson[2022-07-03]
OMIM:310980	Omphalocele		HP:0001539	OMIM:310980	IEA					P	HPO:iea[2009-02-17]
OMIM:310980	Omphalocele		HP:0001417	OMIM:310980	IEA					I	HPO:iea[2009-02-17]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000494	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000750	PMID:32197073	PCS		6/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000463	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0002002	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0002079	PMID:32197073	PCS		2/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0001250	PMID:32197073	PCS		2/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0011968	PMID:32197073	PCS		5/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0002120	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000490	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0001290	PMID:32197073	PCS		3/4			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0001270	PMID:32197073	PCS		6/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0100023	PMID:32197073	PCS					P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0009890	PMID:32197073	IEA		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000748	PMID:32197073	PCS		2/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000729	PMID:32197073	PCS		3/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0007099	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0002714	OMIM:618859	TAS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0001488	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0001257	PMID:32197073	PCS		4/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000006	PMID:32197073	PCS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0000248	PMID:32197073	PCS		1/6			P	HPO:probinson[2020-08-12]
OMIM:618859	Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities		HP:0001249	PMID:32197073	PCS		6/6			P	HPO:probinson[2020-08-12]
OMIM:618681	Lessel-Kubisch syndrome		HP:0000089	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0004322	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0000083	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0000160	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0000822	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0000007	PMID:28846075	PCS					I	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0002216	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0001620	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0000135	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0002225	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17];HPO:probinson[2020-07-17]
OMIM:618681	Lessel-Kubisch syndrome		HP:0000446	PMID:28846075	PCS		1/1			P	HPO:probinson[2020-07-17]
OMIM:174500	Polydactyly, preaxial II		HP:0001177	PMID:18178630	PCS		HP:0040281			P	HPO:iea[2009-10-29]
OMIM:174500	Polydactyly, preaxial II		HP:0009606	OMIM:174500	TAS					P	HPO:skoehler[2012-10-17]
OMIM:174500	Polydactyly, preaxial II		HP:0001162	PMID:18178630	PCS		HP:0040282			P	HPO:iea[2009-10-29]
OMIM:174500	Polydactyly, preaxial II		HP:0010066	OMIM:174500	TAS		HP:0040282			P	HPO:sdoelken[2009-02-17]
OMIM:174500	Polydactyly, preaxial II		HP:0009942	OMIM:174500	TAS		HP:0040281			P	HPO:sdoelken[2009-10-29]
OMIM:174500	Polydactyly, preaxial II		HP:0001841	PMID:18178630	PCS		HP:0040282			P	HPO:iea[2009-10-28]
OMIM:174500	Polydactyly, preaxial II		HP:0001830	PMID:18178630	PCS		HP:0040282			P	HPO:iea[2009-10-29]
OMIM:174500	Polydactyly, preaxial II		HP:0001159	PMID:18178630	PCS		HP:0040282			P	HPO:iea[2009-10-29]
OMIM:174500	Polydactyly, preaxial II		HP:0000006	PMID:12837695	PCS					I	HPO:iea[2009-02-17]
OMIM:174500	Polydactyly, preaxial II		HP:0005866	OMIM:174500	PCS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:605808	Birdshot chorioretinopathy		HP:0100832	PMID:25667738	PCS					P	HPO:probinson[2022-05-04]
OMIM:605808	Birdshot chorioretinopathy		HP:0012123	PMID:10896989	PCS					P	HPO:probinson[2015-07-19]
OMIM:605808	Birdshot chorioretinopathy		HP:0003596	PMID:25667738	PCS					C	HPO:probinson[2022-05-04]
OMIM:605808	Birdshot chorioretinopathy		HP:0000505	PMID:10896989	PCS					P	HPO:probinson[2015-07-19]
OMIM:605808	Birdshot chorioretinopathy		HP:0011531	PMID:10896989	PCS					P	HPO:probinson[2015-07-19]
OMIM:605808	Birdshot chorioretinopathy		HP:0000532	OMIM:605808	TAS					P	HPO:probinson[2009-02-17]
OMIM:605808	Birdshot chorioretinopathy		HP:0007722	PMID:18378316	PCS					P	HPO:probinson[2015-07-19]
OMIM:605808	Birdshot chorioretinopathy		HP:0000006	OMIM:605808	TAS					I	HPO:probinson[2009-02-17]
OMIM:620478	Thrombocytopenia 9		HP:0001892	PMID:28466964;PMID:32150607	PCS		4/14		HP:0012825	P	HPO:probinson[2024-02-11]
OMIM:620478	Thrombocytopenia 9		HP:6000021	PMID:32150607	PCS		4/4			P	HPO:probinson[2024-04-03]
OMIM:620478	Thrombocytopenia 9		HP:0030402	PMID:28466964	PCS		0/2			P	HPO:probinson[2024-02-11]
OMIM:620478	Thrombocytopenia 9		HP:0001873	PMID:28466964;PMID:32150607	PCS		10/10		HP:0012825;HP:0012825	P	HPO:probinson[2024-02-11]
OMIM:620478	Thrombocytopenia 9		HP:0000006	PMID:28466964	PCS					I	HPO:probinson[2024-02-11]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0001396	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0010307	PMID:38821050	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0001250	PMID:38821050	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0002240	PMID:38821050	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0002020	PMID:38821050	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0003593	PMID:38821050	PCS		4/4			C	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0033725	PMID:38821050	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0034782	PMID:38821050	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0001508	PMID:38821050	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0034341	PMID:38821050	PCS					I	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0000998	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0001643	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0001744	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0200020	PMID:38821050	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0003642	PMID:38821050	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0008936	PMID:38821050	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0002650	PMID:38821050	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0002870	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0011344	PMID:38821050	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0002093	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:6000988	PMID:38821050	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0011471	PMID:38821050	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0008064	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0034671	PMID:38821050	PCS		3/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0000407	PMID:38821050	PCS		3/3			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0001999	PMID:38821050	PCS		4/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0000964	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0002104	PMID:38821050	PCS		2/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:301133	Congenital disorder of glycosylation, type 1DD		HP:0034391	PMID:38821050	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-25]
OMIM:136900	Sorsby fundus dystrophy		HP:0011462	PMID:7894485	PCS					C	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:136900	Sorsby fundus dystrophy		HP:0000618	OMIM:136900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:136900	Sorsby fundus dystrophy		HP:0007754	PMID:7894485	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:136900	Sorsby fundus dystrophy		HP:0000006	PMID:7894485	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:136900	Sorsby fundus dystrophy		HP:0000512	OMIM:136900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:136900	Sorsby fundus dystrophy		HP:0000501	OMIM:136900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:136900	Sorsby fundus dystrophy		HP:0000533	PMID:7894485	PCS					P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0002153	PMID:22634753	PCS		0/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0001250	OMIM:614736	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0003154	PMID:22634753	PCS		15/15			P	HPO:probinson[2023-02-18]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0040084	PMID:22634753	PCS		0/15			P	HPO:probinson[2023-02-18]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0040085	PMID:22634753	PCS		0/15			P	HPO:probinson[2023-02-18]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0008163	PMID:22634753	PCS		15/15			P	HPO:probinson[2023-02-18]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0001508	OMIM:614736	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0000826	OMIM:614736	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0002902	PMID:22634753	PCS		0/15			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-18]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0000007	PMID:22634753	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-18]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0001943	OMIM:614736	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0000851	OMIM:614736	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0000028	OMIM:614736	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0000127	OMIM:614736	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:614736	Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency		HP:0001325	OMIM:614736	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0003577	PMID:9445165	PCS		1/1			C	HPO:probinson[2022-07-16]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0006682	PMID:9445165	PCS		1/1			P	HPO:probinson[2022-07-16]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0000007	PMID:9445165	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2022-07-16]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0001657	PMID:9445165	PCS		1/1			P	HPO:probinson[2013-04-06];HPO:probinson[2022-07-16]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0001279	PMID:9445165	PCS		1/1			P	HPO:probinson[2013-04-06];HPO:probinson[2022-07-16]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0001664	OMIM:612347	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0008527	PMID:9445165	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-07-16]
OMIM:612347	Jervell and Lange-Nielsen syndrome 2		HP:0001645	OMIM:612347	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614050	Atrial fibrillation, familial, 12		HP:0003596	PMID:17245405	PCS		1/1			C	HPO:probinson[2022-03-03]
OMIM:614050	Atrial fibrillation, familial, 12		HP:0004757	PMID:17245405	PCS		1/1			P	HPO:skoehler[2013-06-11];HPO:probinson[2022-03-03]
OMIM:614050	Atrial fibrillation, familial, 12		HP:0000006	PMID:17245405	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-03]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0031108	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0003577	PMID:32065591	PCS		3/8			C	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0010307	PMID:32065591	PCS		8/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0031629	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0001252	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0010829	PMID:32065591	PCS		4/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0002460	PMID:32065591	PCS		4/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0002380	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0003392	PMID:32065591	PCS		2/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0031986	PMID:32065591	PCS		2/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0011463	PMID:32065591	PCS		5/8			C	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0009027	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0001604	PMID:32065591	PCS		8/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0008954	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0007328	PMID:32065591	PCS		3/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0002751	PMID:32065591	PCS		2/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0003687	PMID:32065591	PCS		1/1			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0002015	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0002650	PMID:32065591	PCS		2/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0031936	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0001761	PMID:32065591	PCS		6/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0002076	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0030166	PMID:32065591	PCS		3/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0012046	PMID:32065591	PCS		4/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0000969	PMID:32065591	PCS		2/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0100759	PMID:32065591	PCS		1/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0006886	PMID:32065591	PCS		4/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0002522	PMID:32065591	PCS		5/8			P	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0000006	PMID:32065591	PCS					I	HPO:probinson[2021-11-20]
OMIM:619574	Charcot-Marie-Tooth disease, axonal, type 2HH		HP:0001337	PMID:32065591	PCS		2/8			P	HPO:probinson[2021-11-20]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0001298	OMIM:616647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0000252	PMID:26224535	PCS		5/7			P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0002059	OMIM:616647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0002133	PMID:26224535	PCS					P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0002188	PMID:26224535	PCS					P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0011968	PMID:26224535	PCS		6/7			P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0001250	PMID:26224535	PCS		7/7			P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0001263	PMID:26224535	PCS		6/6			P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0006829	OMIM:616647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0003593	PMID:26224535	PCS					C	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0012444	PMID:26224535	PCS					P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0000518	PMID:26224535	PCS		3/7			P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0000737	PMID:26224535	PCS					P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0000007	PMID:26224535	PCS					I	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0001638	OMIM:616647	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0001522	PMID:26224535	PCS					C	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0001511	OMIM:616647	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0001620	PMID:26224535	PCS					P	HPO:probinson[2017-06-17]
OMIM:616647	Epileptic encephalopathy, early infantile, 35		HP:0200085	PMID:26224535	PCS					P	HPO:probinson[2017-06-17]
OMIM:612353	Porokeratosis 6, disseminated superficial Actinic type		HP:0200044	OMIM:612353	TAS					P	HPO:skoehler[2012-11-16]
OMIM:612353	Porokeratosis 6, disseminated superficial Actinic type		HP:0000006	OMIM:612353	TAS					I	HPO:skoehler[2012-11-16]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001254	PMID:12838198	IEA		9/15			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:6001023	PMID:7738175	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0002686	OMIM:609015	IEA					H	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001396	PMID:12838198	PCS		2/15			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003236	PMID:12838198	PCS		7/8			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003198	OMIM:609015	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001252	PMID:12838198	PCS		14/17			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003394	PMID:12838198	IEA		5/15			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0000580	PMID:12838198	PCS		2/16			P	HPO:probinson[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003593	PMID:12838198	PCS		11/21			C	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:6001024	PMID:7738175	PCS		1/1			P	HPO:probinson[2024-08-03]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0011675	PMID:12838198	PCS		2/17			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001508	PMID:12838198	PCS		7/10			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0002913	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001789	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001987	PMID:12838198	PCS		8/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0002878	OMIM:609015	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0002910	OMIM:609015	TAS					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001644	PMID:12838198	PCS		8/11			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001985	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003128	PMID:12838198	PCS		13/17			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003326	OMIM:609015	TAS					P	HPO:skoehler[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003623	PMID:12838198	PCS		10/21			C	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003324	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0031956	PMID:12838198	PCS		7/15			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0003201	OMIM:609015	TAS					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0011968	PMID:12838198	PCS		9/10			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001560	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001263	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001284	PMID:12838198	PCS		7/9			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0045045	PMID:12838198	PCS		12/12			P	HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0002093	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001518	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0009830	PMID:12838198	PCS		11/14			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-06-26]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0000007	OMIM:609015	IEA					I	HPO:iea[2009-02-17]
OMIM:609015	Mitochondrial trifunctional protein deficiency		HP:0001635	OMIM:609015	IEA					P	HPO:iea[2009-02-17]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000365	PMID:29180823	PCS		4/18			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001773	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000486	PMID:29180823	PCS		13/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0004322	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000243	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001371	PMID:29180823	PCS		5/17			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001250	OMIM:309590	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000160	PMID:29180823	PCS		1/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0003196	PMID:29180823	PCS		8/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0003593	OMIM:309590	IEA					C	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001290	PMID:29180823	PCS		14/20			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0012745	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000639	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000316	PMID:29180823	IEA		7/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001845	PMID:29180823	PCS		9/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000752	PMID:29180823	PCS		4/16			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001249	PMID:29180823;PMID:18252223	PCS		25/25			P	HPO:probinson[2021-09-28];HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000677	PMID:29180823	PCS		2/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000358	OMIM:309590	IEA		8/19			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0002311	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0003202	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000494	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000252	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000054	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001264	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001344	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0002750	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0002079	PMID:29180823	PCS		2/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000490	PMID:29180823	PCS		15/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001263	PMID:29180823	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001182	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0012385	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000767	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000601	PMID:29180823	PCS		6/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000648	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001417	PMID:18252223	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2021-09-28]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000565	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000047	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000322	PMID:29180823	PCS		10/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000248	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000369	PMID:29180823	PCS		7/19			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000325	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001792	PMID:29180823	PCS		4/19			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000582	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000343	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001156	PMID:29180823	PCS		12/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000540	PMID:29180823	PCS		7/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000581	PMID:29180823	PCS		12/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0002162	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001270	PMID:29180823	PCS		20/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000414	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000733	PMID:29180823	PCS		8/17			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000219	PMID:29180823	PCS		16/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0002119	PMID:29180823	PCS		4/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0030084	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000537	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000218	PMID:29180823	PCS		1/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000455	PMID:29180823	PCS		15/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000378	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000411	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000256	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000179	PMID:29180823	PCS		6/21			P	HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001347	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000154	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0002059	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001363	PMID:29180823	PCS		2/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000750	PMID:29180823;PMID:18252223	PCS		15/16			P	HPO:probinson[2021-09-28];HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0002650	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0031936	PMID:29180823	PCS		16/19			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000276	PMID:29180823;PMID:18252223	PCS		12/27			P	HPO:probinson[2021-09-28];HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0005280	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0001518	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000508	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000348	PMID:29180823	PCS		13/21			P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0200055	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000028	PMID:29180823	PCS		3/7	MALE		P	HPO:skoehler[2019-09-07];HPO:probinson[2021-02-20]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000347	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:309590	Intellectual developmental disorder, X-linked syndromic, Turner type		HP:0000545	OMIM:309590	IEA					P	HPO:skoehler[2019-09-07]
OMIM:601449	Deafness, progressive, with stapes fixation		HP:0000381	OMIM:601449	TAS					P	HPO:probinson[2013-03-10]
OMIM:601449	Deafness, progressive, with stapes fixation		HP:0000007	OMIM:601449	TAS					I	HPO:probinson[2009-02-17]
OMIM:601449	Deafness, progressive, with stapes fixation		HP:0008513	OMIM:601449	TAS					P	HPO:probinson[2009-02-17]
OMIM:600757	Orofacial cleft 3		HP:0000271	OMIM:600757	IEA					P	HPO:iea[2009-02-17]
OMIM:600757	Orofacial cleft 3		HP:0000006	OMIM:600757	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:272650	Tatsumi factor deficiency		HP:0001892	OMIM:272650	IEA					P	HPO:iea[2009-02-17]
OMIM:272650	Tatsumi factor deficiency		HP:0003010	OMIM:272650	IEA					P	HPO:iea[2009-02-17]
OMIM:272650	Tatsumi factor deficiency		HP:0000007	OMIM:272650	IEA					I	HPO:iea[2009-02-17]
OMIM:272650	Tatsumi factor deficiency		HP:0003337	OMIM:272650	IEA					P	HPO:iea[2009-02-17]
OMIM:613065	Leukemia, acute lymphocytic, susceptibility to, 1		HP:0001442	OMIM:613065	TAS					I	HPO:probinson[2020-07-14]
OMIM:613065	Leukemia, acute lymphocytic, susceptibility to, 1		HP:0010982	OMIM:613065	TAS					I	HPO:probinson[2013-04-14]
OMIM:613065	Leukemia, acute lymphocytic, susceptibility to, 1		HP:0006721	OMIM:613065	TAS					P	HPO:probinson[2013-04-14]
OMIM:604519	Inflammatory bowel disease 3		HP:0100279	OMIM:604519	TAS					P	HPO:skoehler[2017-07-13]
OMIM:604519	Inflammatory bowel disease 3		HP:0000006	OMIM:604519	TAS					I	HPO:skoehler[2017-07-13]
OMIM:277700	Werner syndrome		HP:0025441	PMID:30891318;PMID:30568144	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0000320	PMID:30568144	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0004322	PMID:30891318;OMIM:277700	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-06-03];HPO:iea[2009-02-17]
OMIM:277700	Werner syndrome		HP:0007618	OMIM:277700	IEA					P	HPO:iea[2009-02-17]
OMIM:277700	Werner syndrome		HP:0005177	PMID:30891318;OMIM:277700	PCS		10/11			P	ORCID:0000-0002-0736-9199[2024-06-03];HPO:iea[2009-02-17]
OMIM:277700	Werner syndrome		HP:0033047	PMID:30568144	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0003074	PMID:30891318;PMID:30568144	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0031964	PMID:30568144	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0000819	PMID:30891318;PMID:30568144	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-03];HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0000939	OMIM:277700;PMID:30568144	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-06-03];HPO:iea[2009-02-17]
OMIM:277700	Werner syndrome		HP:0100324	OMIM:277700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:277700	Werner syndrome		HP:0000518	PMID:30891318;PMID:30568144	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-03];HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0011462	PMID:30891318	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0002858	PMID:30891318;OMIM:277700;PMID:30568144	PCS		10/12			P	HPO:skoehler[2010-06-20];ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0040217	PMID:30891318;PMID:30568144	PCS		2/2			P	HPO:probinson[2022-05-14];ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0002216	PMID:30891318;PMID:30568144	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0001620	PMID:30891318;PMID:30568144	PCS		2/2			P	HPO:probinson[2022-05-14];ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0000135	OMIM:277700	IEA					P	HPO:iea[2009-02-17]
OMIM:277700	Werner syndrome		HP:0005328	PMID:30891318;PMID:30568144	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-14];ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0031956	PMID:30568144	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0003621	PMID:30568144	PCS		1/1			C	HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0004334	PMID:30891318;PMID:30568144	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0002155	PMID:30891318;PMID:30568144	PCS		2/2			P	HPO:probinson[2022-05-14];ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0002293	PMID:30568144	PCS	HP:0011462	1/1			P	HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0007495	PMID:30568144	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0003419	PMID:30568144	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0000007	PMID:8602509	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-14]
OMIM:277700	Werner syndrome		HP:0000546	PMID:30891318;OMIM:277700;PMID:30568144	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-06-03];HPO:iea[2009-02-17]
OMIM:277700	Werner syndrome		HP:0002669	PMID:30891318;OMIM:277700;PMID:30568144	PCS		10/12			P	HPO:probinson[2009-02-17];ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0000444	PMID:30891318;PMID:30568144	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-03];HPO:iea[2009-02-17];HPO:probinson[2024-06-03]
OMIM:277700	Werner syndrome		HP:0008404	PMID:30891318	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0007556	PMID:30891318	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0002863	PMID:30891318;PMID:30568144	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-03]
OMIM:277700	Werner syndrome		HP:0004349	PMID:30568144	PCS		1/1			P	HPO:probinson[2022-05-14]
OMIM:615414	Microcephaly 11, primary, autosomal recessive		HP:0000252	PMID:23418308	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-03-04]
OMIM:615414	Microcephaly 11, primary, autosomal recessive		HP:0004322	PMID:23418308	PCS		2/2			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-03-04]
OMIM:615414	Microcephaly 11, primary, autosomal recessive		HP:0000007	PMID:23418308	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2023-03-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0001760	OMIM:608323	IEA					P	HPO:iea[2009-02-17]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0030237	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0003431	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0001288	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0003484	OMIM:608323	IEA					P	HPO:probinson[2012-03-13]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0003693	PMID:24354524	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0003383	PMID:24354524	PCS		0/1			P	HPO:skoehler[2013-05-31];HPO:probinson[2024-03-13]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0002460	PMID:24354524	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0003450	OMIM:608323	IEA					P	HPO:iea[2009-02-17]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0001284	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0025709	PMID:24354524	PCS		1/1			C	HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0009046	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0002936	PMID:24354524	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0003448	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:608323	Charcot-Marie-Tooth disease, dominant intermediate C		HP:0000006	PMID:16429158	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-12]
OMIM:617565	Perrault syndrome 6		HP:0008209	PMID:28449065	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-10]
OMIM:617565	Perrault syndrome 6		HP:0000013	PMID:28449065	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-10]
OMIM:617565	Perrault syndrome 6		HP:0000869	PMID:28449065	PCS		1/2	FEMALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2020-08-10]
OMIM:617565	Perrault syndrome 6		HP:0000407	PMID:28449065	PCS		2/2			P	HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:617565	Perrault syndrome 6		HP:0000858	PMID:28449065	PCS					P	HPO:probinson[2020-08-10]
OMIM:617565	Perrault syndrome 6		HP:0000007	PMID:28449065	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2020-08-10]
OMIM:617565	Perrault syndrome 6		HP:0010464	PMID:28449065	PCS		1/1			P	HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:617565	Perrault syndrome 6		HP:0000786	PMID:28449065	PCS		1/2	FEMALE		P	HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000286	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0030953	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000750	PMID:34102099	PCS		3/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0001250	PMID:34102099	PCS		2/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0001382	PMID:34102099	PCS		2/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0001274	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0001263	PMID:34102099	PCS		3/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0001252	PMID:34102099	PCS		3/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000718	PMID:34102099	PCS		2/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000316	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000767	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000007	PMID:34102099	PCS					I	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000218	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0004626	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0001257	PMID:34102099	PCS		3/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0001249	PMID:34102099	PCS		3/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000336	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000369	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:619548	Usmani-Riazuddin syndrome, autosomal recessive		HP:0000358	PMID:34102099	PCS		1/3			P	HPO:probinson[2022-01-23]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001399	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0002243	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000023	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001252	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0003075	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0002240	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001290	OMIM:235255	TAS					P	HPO:skoehler[2017-07-13]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0003270	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0009085	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001629	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000319	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0006273	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000316	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000998	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000219	OMIM:235255	IEA					P	HPO:skoehler[2010-06-20]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0002119	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000218	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000774	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001522	OMIM:235255	IEA					C	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001004	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0005989	OMIM:235255	TAS					P	HPO:skoehler[2015-01-20]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001744	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0005469	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000054	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000175	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000494	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001561	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000431	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000474	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001541	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0001162	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000272	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000470	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0011800	OMIM:235255	TAS					P	HPO:skoehler[2015-11-15]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000007	OMIM:235255	IEA					I	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0002901	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0006521	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000520	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000028	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000347	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000369	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0000126	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:235255	Mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly		HP:0008229	OMIM:235255	IEA					P	HPO:iea[2009-02-17]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0000639	PMID:19864492	PCS					P	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0010984	PMID:19864492	PCS					I	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0007750	PMID:19864492	PCS					P	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0000505	PMID:19864492	TAS					P	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0007633	PMID:19864492	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0009911	PMID:19864492	PCS		1/2			P	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0007766	PMID:19864492	PCS					P	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0000589	PMID:19864492	PCS		HP:0040281			P	HPO:iea[2012-04-24]
OMIM:613703	Microphthalmia, isolated, with coloboma 6		HP:0000006	PMID:19864492	PCS					I	HPO:iea[2012-04-24]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000286	PMID:31044565	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0003213	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0003214	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0003577	PMID:16429406;PMID:22701786	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000486	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0020073	PMID:31044565	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000365	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0004322	PMID:31044565;PMID:16429406;PMID:22701786	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001371	PMID:22701786	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000086	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000085	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000081	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001909	PMID:16429406	PCS		0/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001629	PMID:22701786	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000815	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0011463	PMID:31044565	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000957	PMID:31044565;PMID:16429406;PMID:22701786	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2021-02-18];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001903	PMID:31044565;PMID:16429406	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:skoehler[2012-10-17];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000953	PMID:8128956	PCS		1/1			P	HP:probinson[2019-05-17];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0009942	PMID:31044565;PMID:22701786	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-19]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000978	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0005528	PMID:31044565;PMID:22701786	PCS		2/2			P	HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0009943	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001249	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000252	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0003221	PMID:31044565;PMID:16429406;PMID:22701786	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0011940	PMID:31044565	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001518	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000568	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000007	PMID:1574115	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0009777	PMID:31044565;PMID:16429406;PMID:22701786	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001896	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001511	PMID:22701786	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001873	PMID:16429406;PMID:8128956	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:skoehler[2012-10-17];HP:probinson[2019-05-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0009778	PMID:31044565;PMID:22701786	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000325	PMID:22701786	PCS		1/1			P	HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001876	PMID:31044565;PMID:16429406	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2021-02-18]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000028	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0003974	PMID:31044565;PMID:16429406;PMID:22701786	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HPO:probinson[2024-04-19]
OMIM:227645	Fanconi anemia, complementation group C		HP:0000104	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001875	PMID:16429406;PMID:8128956	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-04-19];HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:227645	Fanconi anemia, complementation group C		HP:0001017	OMIM:227645	IEA					P	HPO:iea[2009-02-17]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0003577	PMID:21549340	PCS		4/4			C	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000365	PMID:21549340	PCS		4/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0001234	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0001377	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0001773	OMIM:614078	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0001156	PMID:21549340	PCS		2/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0004322	PMID:21549340	PCS		4/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000160	OMIM:614078	TAS					P	HPO:skoehler[2012-11-18]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0004440	PMID:21549340	PCS		2/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0003196	OMIM:614078	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0010049	PMID:21549340	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0012368	PMID:21549340	PCS		2/4			P	HPO:skoehler[2013-10-22];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0002999	PMID:21549340	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0002857	PMID:21549340	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0004976	PMID:21549340	PCS		5/8			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0003048	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0003026	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000175	PMID:21549340	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0001385	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0009826	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000431	PMID:21549340	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0001241	PMID:21549340	PCS		2/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0005001	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0009190	PMID:21549340	PCS		1/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000007	PMID:21549340	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000348	PMID:21549340	PCS		2/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0002945	PMID:21549340	PCS		2/4			P	HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000520	PMID:21549340	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0000347	PMID:21549340	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614078	Chondrodysplasia with joint dislocations, Gpapp type		HP:0001831	OMIM:614078	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613717	Treacher collins syndrome 2		HP:0000175	PMID:21131976;PMID:24603435	PCS		4/13			P	HPO:probinson[2022-11-10];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0003577	PMID:24603435	PCS		2/4			C	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000494	PMID:21131976;PMID:24603435	PCS		9/12			P	HPO:probinson[2022-11-10];HPO:skoehler[2012-11-20];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0004467	PMID:24603435	PCS		1/4			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000453	PMID:21131976	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000750	PMID:21131976	PCS		2/7			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000452	PMID:21131976	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0005473	PMID:24603435	PCS		1/4			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000272	PMID:24603435	PCS		3/4			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0001270	PMID:21131976	PCS		1/7			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0010669	PMID:21131976	PCS		5/8			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0009892	PMID:24603435	PCS		1/4			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000308	PMID:24603435	PCS		2/4			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0008551	PMID:21131976	PCS		7/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000007	PMID:24603435	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000405	PMID:21131976;PMID:24603435	PCS		8/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-10];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000652	PMID:21131976	PCS		3/8			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000278	PMID:24603435	PCS		1/4			P	HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000006	PMID:21131976	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:613717	Treacher collins syndrome 2		HP:0000347	PMID:21131976;PMID:24603435	PCS		11/13			P	HPO:probinson[2022-11-10];HPO:skoehler[2012-10-17];HPO:probinson[2022-11-10]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0003577	PMID:28575648	PCS		6/6			C	HPO:probinson[2022-12-04]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0040189	PMID:28575648	PCS		6/6			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-12-04]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0000007	PMID:28575648	PCS					I	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-12-04]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0025080	PMID:28575648	PCS		1/1			P	HPO:nvasilevsky[2019-02-25];HPO:probinson[2022-12-04]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0000989	PMID:28575648	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-04]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0010783	PMID:28575648	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-04]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0007479	PMID:28575648	PCS		4/6			P	HPO:probinson[2022-12-04]
OMIM:617571	Ichthyosis, congenital, autosomal recessive 14		HP:0000962	PMID:28575648	PCS		6/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-04]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0002652	OMIM:182255	IEA					P	HPO:iea[2009-02-17]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0002663	OMIM:182255	TAS					P	HPO:probinson[2012-05-14]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0004322	OMIM:182255	IEA					P	HPO:iea[2009-02-17]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0010034	OMIM:182255	IEA					P	HPO:iea[2009-02-17]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0005819	OMIM:182255	TAS					P	HPO:probinson[2009-02-17]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0004209	OMIM:182255	IEA					P	HPO:iea[2009-02-17]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0009844	OMIM:182255	TAS					P	HPO:probinson[2013-04-07]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0000006	OMIM:182255	IEA					I	HPO:iea[2009-02-17]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0010579	OMIM:182255	IEA					P	HPO:iea[2009-02-17]
OMIM:182255	Skeletal dysplasia with delayed epiphyseal and carpal bone ossification		HP:0001216	OMIM:182255	TAS					P	HPO:probinson[2012-05-14]
OMIM:609029	Emanuel syndrome		HP:0001650	OMIM:609029	IEA		28/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001374	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000483	PMID:19606488	PCS		8/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002023	PMID:19606488	PCS		9/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000365	PMID:19606488	PCS		45/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000486	PMID:19606488	PCS		21/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000089	PMID:19606488	PCS		11/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000122	PMID:19606488	PCS		8/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001250	PMID:19606488	PCS		30/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000680	PMID:19606488	PCS		50/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001252	OMIM:609029;PMID:19606488	PCS		51/73			P	HPO:probinson[2023-02-24];HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0002020	PMID:19606488	PCS		34/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000678	PMID:19606488	PCS		23/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000238	PMID:19606488	PCS		11/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001643	PMID:19606488	PCS		7/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002019	PMID:19606488	PCS		40/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001642	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0001249	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000175	PMID:19606488	PCS		34/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000252	PMID:19606488	PCS		14/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000054	PMID:19606488	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001660	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000010	PMID:19606488	PCS		11/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002079	PMID:19606488	PCS		12/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0011968	OMIM:609029	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609029	Emanuel syndrome		HP:0000490	OMIM:609029	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609029	Emanuel syndrome		HP:0001263	OMIM:609029	TAS		63/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0034392	PMID:19606488	PCS		9/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0009098	PMID:19606488	PCS		7/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000403	PMID:19606488	PCS		61/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002307	PMID:19606488	PCS		47/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000400	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000960	PMID:19606488	PCS		15/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000369	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000324	OMIM:609029	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609029	Emanuel syndrome		HP:0004467	PMID:19606488	PCS		96/126			P	HPO:probinson[2023-02-24];HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000384	PMID:19606488	PCS		21/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000582	OMIM:609029	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609029	Emanuel syndrome		HP:0003577	PMID:19606488	PCS		63/63			C	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000343	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0002562	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000023	PMID:19606488	PCS		9/63			P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0001195	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0012802	OMIM:609029	TAS					P	HPO:skoehler[2014-06-24]
OMIM:609029	Emanuel syndrome		HP:0001629	PMID:19606488	PCS		8/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001508	PMID:19606488	PCS		39/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001305	PMID:19606488	PCS		5/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002119	PMID:19606488	PCS		17/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000218	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0009765	OMIM:609029	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609029	Emanuel syndrome		HP:0000776	OMIM:609029;PMID:19606488	PCS		15/73			P	HPO:probinson[2023-02-24];HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0001622	PMID:19606488	PCS		6/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001562	PMID:19606488	PCS		10/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000473	PMID:19606488	PCS		9/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002059	OMIM:609029	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609029	Emanuel syndrome		HP:0000750	OMIM:609029	TAS					P	HPO:skoehler[2012-10-17]
OMIM:609029	Emanuel syndrome		HP:0002650	PMID:19606488	PCS		20/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000474	OMIM:609029;PMID:19606488	PCS		25/73			P	HPO:probinson[2023-02-24];HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0011108	PMID:19606488	PCS		21/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002808	PMID:19606488	PCS		19/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001558	PMID:19606488	PCS		11/63			P	HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001511	PMID:19606488	PCS		15/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002205	PMID:19606488	PCS		30/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0001631	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000028	OMIM:609029	IEA					P	HPO:iea[2009-02-17]
OMIM:609029	Emanuel syndrome		HP:0000347	PMID:19606488	PCS		38/63			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0000545	PMID:19606488	PCS		24/63			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-24]
OMIM:609029	Emanuel syndrome		HP:0002566	PMID:19606488	PCS		5/63			P	HPO:probinson[2023-02-24]
OMIM:617217	Amelogenesis imperfecta, hypomaturation type, IIA6		HP:0000705	PMID:27693231	PCS					P	HPO:probinson[2021-02-13]
OMIM:617217	Amelogenesis imperfecta, hypomaturation type, IIA6		HP:0009102	PMID:27693231	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:617217	Amelogenesis imperfecta, hypomaturation type, IIA6		HP:0006285	PMID:27693231	PCS					P	HPO:probinson[2021-02-13]
OMIM:617217	Amelogenesis imperfecta, hypomaturation type, IIA6		HP:0000007	PMID:27693231	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-13]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0003477	PMID:24123876	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0008209	PMID:28633435	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0003577	PMID:28969388	PCS		1/4			C	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0000486	PMID:28969388;PMID:28633435	PCS		4/13			P	HPO:probinson[2022-06-08];HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001256	PMID:28969388;PMID:24123876	PCS		4/6			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0004322	PMID:28633435	PCS		3/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001252	PMID:24123876	PCS		2/2			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001251	PMID:24123876	PCS		2/2			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002460	PMID:28969388	PCS		4/4			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001270	PMID:28969388	PCS		2/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001171	PMID:28969388	PCS		2/4			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0007141	PMID:28633435	PCS		9/9			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0011463	PMID:28969388	PCS		1/4			C	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0009027	OMIM:618124	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002936	OMIM:618124	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002317	PMID:28969388	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001249	PMID:28633435	PCS		7/9			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0007328	PMID:28633435	PCS		1/9			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001265	PMID:28969388	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0003621	PMID:28969388	PCS		2/4			C	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0000750	PMID:28969388	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002650	PMID:28969388;PMID:28633435	PCS		3/13			P	HPO:probinson[2022-06-08];HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002870	PMID:28633435	PCS		1/9			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0000496	OMIM:618124	IEA		HP:0040284			P	HPO:skoehler[2019-02-15]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0031936	PMID:28633435	PCS		5/9			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001761	PMID:28969388	PCS		2/4			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002808	PMID:28969388	PCS		1/4			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0000602	PMID:28969388	PCS		1/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0000007	PMID:28633435	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002705	OMIM:618124	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002505	PMID:28633435	PCS	HP:0003621	6/8			P	HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0001513	PMID:28633435	PCS		2/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0003677	PMID:28633435	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2022-06-08]
OMIM:618124	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development		HP:0002522	PMID:28633435	PCS		6/9			P	HPO:probinson[2022-06-08]
OMIM:607004	Brachydactyly, type A1, B		HP:0009370	OMIM:607004	TAS					P	HPO:probinson[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0004322	OMIM:607004	IEA					P	HPO:iea[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0010230	OMIM:607004	IEA					P	HPO:iea[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0008111	OMIM:607004	TAS					P	HPO:probinson[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0009882	OMIM:607004	IEA					P	HPO:iea[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0005819	OMIM:607004	IEA					P	HPO:iea[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0009466	OMIM:607004	IEA					P	HPO:iea[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0010047	OMIM:607004	IEA					P	HPO:iea[2009-02-17]
OMIM:607004	Brachydactyly, type A1, B		HP:0030084	OMIM:607004	TAS					P	HPO:skoehler[2014-09-21]
OMIM:607004	Brachydactyly, type A1, B		HP:0000006	OMIM:607004	IEA					I	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0002751	OMIM:109500	IEA					P	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0002277	OMIM:109500	IEA					P	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0003396	OMIM:109500	TAS					P	HPO:probinson[2013-03-30]
OMIM:109500	Basilar impression, primary		HP:0004484	OMIM:109500	IEA					P	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0003828	OMIM:109500	TAS					M	HPO:skoehler[2013-04-02]
OMIM:109500	Basilar impression, primary		HP:0000470	OMIM:109500	IEA					P	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0002691	OMIM:109500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:109500	Basilar impression, primary		HP:0003829	OMIM:109500	IEA					I	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0003690	OMIM:109500	IEA					P	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0002318	OMIM:109500	IEA					P	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0005758	OMIM:109500	IEA					P	HPO:iea[2009-02-17]
OMIM:109500	Basilar impression, primary		HP:0000006	OMIM:109500	IEA					I	HPO:iea[2009-02-17]
OMIM:613071	Bronchiectasis with or without elevated sweat chloride 3		HP:0002110	OMIM:613071	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613071	Bronchiectasis with or without elevated sweat chloride 3		HP:0000006	OMIM:613071	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613071	Bronchiectasis with or without elevated sweat chloride 3		HP:0004469	OMIM:613071	IEA					P	HPO:skoehler[2010-06-19]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0002069	PMID:23518707	PCS		5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0003621	PMID:23518707	PCS		5/5			C	HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0033715	PMID:23518707	PCS		1/5			P	HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0011182	PMID:23518707	PCS		3/5			P	HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0002384	PMID:23518707	PCS		4/5			P	HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0011165	PMID:23518707	PCS		3/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0000007	PMID:23518707	PCS					I	HPO:skoehler[2013-09-30];HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0001337	PMID:23518707	PCS		5/5			P	HPO:skoehler[2015-07-29];HPO:probinson[2022-12-18]
OMIM:615400	Epilepsy, familial adult myoclonic, 5		HP:0001336	PMID:23518707	PCS		5/5			P	HPO:probinson[2022-12-18]
OMIM:612838	Brugada syndrome 5		HP:0001663	PMID:18464934	TAS					P	HPO:probinson[2013-04-07]
OMIM:612838	Brugada syndrome 5		HP:0012251	PMID:18464934	TAS					P	HPO:probinson[2013-04-07]
OMIM:612838	Brugada syndrome 5		HP:0000006	PMID:18464934	TAS					I	HPO:probinson[2013-04-07]
OMIM:612838	Brugada syndrome 5		HP:0011710	PMID:18464934	TAS					P	HPO:probinson[2013-04-07]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001254	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001250	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001252	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0003593	PMID:11170888	PCS		2/5			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001290	OMIM:210200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0002919	OMIM:210200	TAS					P	HPO:probinson[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001508	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0033596	PMID:11170888	PCS		7/7			P	HPO:probinson[2022-09-04]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0033111	PMID:11170888	PCS		7/7			P	HPO:probinson[2022-09-04]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0006573	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0008872	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001943	OMIM:210200	TAS					P	HPO:probinson[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0004911	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001249	OMIM:210200	IEA					P	HPO:skoehler[2010-06-18]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001347	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:4000206	OMIM:210200	TAS					P	HPO:probinson[2024-01-06]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0002179	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0003621	PMID:11170888	PCS		1/5			C	HPO:probinson[2022-09-04]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0002013	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001263	OMIM:210200	IEA		20/20			P	HPO:skoehler[2019-02-22];HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0003581	PMID:11170888	PCS		2/5			C	HPO:probinson[2022-09-04]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0008281	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0000007	PMID:11181649	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-01-30]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0002104	OMIM:210200	IEA					P	HPO:skoehler[2019-09-07]
OMIM:210200	3-Methylcrotonyl-CoA carboxylase 1 deficiency		HP:0001259	OMIM:210200	IEA					P	HPO:iea[2009-02-17]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002069	PMID:29100089	PCS		0/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000286	PMID:29100089	PCS		1/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000486	PMID:29100089	PCS		1/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002121	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001252	PMID:29100089	PCS		7/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0003097	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0003593	PMID:29100089	PCS					C	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001629	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000737	PMID:29100089	PCS		0/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0008551	PMID:29100089	PCS		0/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001548	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002317	PMID:29100089	PCS		0/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002857	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002579	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000256	PMID:29100089	PCS		2/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002236	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001249	PMID:29100089	PCS		14/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000154	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0008936	PMID:29100089	PCS	HP:0003593	1/14			P	HPO:probinson[2025-02-23]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000494	PMID:29100089	PCS		2/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000252	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000054	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001344	PMID:29100089	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000750	PMID:29100089	PCS		13/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002353	PMID:29100089	PCS		2/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0006979	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0031936	PMID:29100089	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002373	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001382	PMID:29100089	PCS		2/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001263	PMID:29100089	PCS		12/14			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002194	PMID:29100089	PCS		12/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0011327	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0007074	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0100814	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0030890	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000601	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000505	PMID:29100089	PCS		0/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0001510	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000006	PMID:29100089	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000248	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000028	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002247	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0002566	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0004305	PMID:29100089	PCS		2/14			P	HPO:probinson[2022-06-16]
OMIM:617798	Intellectual developmental disorder, autosomal dominant 53		HP:0000126	PMID:29100089	PCS		1/14			P	HPO:probinson[2022-06-16]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0002421	PMID:26005868	PCS		3/3			P	HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0003577	PMID:26005868	PCS		3/3			C	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0003676	OMIM:616486	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0000582	PMID:26005868	PCS		0/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0002540	PMID:26005868	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0002365	OMIM:616486	TAS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001250	OMIM:616486	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001252	PMID:26005868	PCS		3/3			P	HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0002064	OMIM:616486	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001251	PMID:26005868	PCS		0/3			P	HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0002119	PMID:26005868	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001347	PMID:26005868	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0000253	OMIM:616486	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0000252	PMID:26005868	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001344	PMID:26005868	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001321	OMIM:616486	TAS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0002079	PMID:26005868	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001263	PMID:26005868	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001285	PMID:26005868	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0011421	PMID:26005868	PCS		1/3			C	HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0003819	PMID:26005868	PCS		2/3			C	HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0000729	PMID:26005868	PCS		2/3			P	HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0000007	PMID:26005868	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-27]
OMIM:616486	Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities		HP:0001776	PMID:26005868	PCS		2/3			P	HPO:probinson[2022-08-27]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0001561	OMIM:214700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0003621	PMID:19861545	PCS		1/5			C	HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0003113	OMIM:214700	IEA					P	HPO:iea[2009-02-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0003593	PMID:19861545	PCS		4/5			C	HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0003270	OMIM:214700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0034470	PMID:19861545	PCS		2/2			P	HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0000859	PMID:19861545	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0001508	OMIM:214700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0001948	OMIM:214700	IEA					P	HPO:iea[2009-02-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0000848	PMID:19861545	PCS		2/2			P	HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0001507	OMIM:214700	IEA					P	HPO:iea[2009-02-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0032067	PMID:19861545	PCS		6/6			P	HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0200114	OMIM:214700	TAS					P	HPO:skoehler[2013-06-05]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0002902	OMIM:214700	IEA					P	HPO:iea[2009-02-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0001944	OMIM:214700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0000007	PMID:19861545	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0002900	PMID:19861545	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0001510	OMIM:214700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0005208	PMID:19861545	PCS		6/6			P	HPO:probinson[2022-12-18]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0001622	OMIM:214700	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214700	Diarrhea 1, secretory chloride, congenital		HP:0000841	OMIM:214700	TAS					P	HPO:skoehler[2013-06-13]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0003577	PMID:25957469	PCS		7/7			C	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000365	OMIM:178110	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0001552	OMIM:178110	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000023	PMID:25957469	PCS		1/7			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0004322	PMID:25957469	PCS		8/9			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0003273	PMID:25957469	PCS		2/4			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0009760	PMID:25957469	PCS		2/9			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0001629	PMID:25957469	PCS		2/7			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0002937	OMIM:178110	IEA					P	HPO:iea[2009-02-17]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0009702	OMIM:178110	IEA					P	HPO:skoehler[2019-09-07]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000358	PMID:25957469	PCS		5/9			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000175	PMID:25957469	PCS		1/7			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0001363	PMID:25957469	PCS		2/7			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000494	PMID:25957469	PCS		7/9			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000252	OMIM:178110	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0003302	PMID:25957469	PCS		1/7			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0002650	OMIM:178110	IEA		7/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0001040	PMID:25957469	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000470	PMID:25957469	PCS		10/10			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0010554	PMID:25957469	PCS		1/7			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0012385	PMID:25957469	PCS		9/9			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0006380	PMID:25957469	PCS		7/10			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0033142	PMID:25957469	PCS		7/9			P	HPO:probinson[2020-10-13];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0002948	PMID:25957469	PCS		5/8			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000508	PMID:25957469	PCS		5/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0002804	OMIM:178110	IEA					P	HPO:skoehler[2015-01-19]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0008445	PMID:25957469	PCS		1/7			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000768	OMIM:178110	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0008368	OMIM:178110	IEA					P	HPO:skoehler[2019-09-07]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0002987	OMIM:178110	TAS					P	HPO:skoehler[2015-07-26]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0009756	PMID:25957469	PCS		5/9			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000465	PMID:25957469	PCS		8/9			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000006	PMID:28205584	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2020-10-13]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0034391	PMID:25957469	PCS		6/9			P	HPO:probinson[2023-02-11]
OMIM:178110	Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A		HP:0000369	PMID:25957469	PCS		5/9			P	HPO:probinson[2023-02-11]
OMIM:167030	Nephrolithiasis, calcium oxalate		HP:0001919	PMID:27210743	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:167030	Nephrolithiasis, calcium oxalate		HP:0003159	PMID:27210743	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:167030	Nephrolithiasis, calcium oxalate		HP:0011463	PMID:27210743	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:167030	Nephrolithiasis, calcium oxalate		HP:0008672	PMID:27210743	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-19]
OMIM:167030	Nephrolithiasis, calcium oxalate		HP:0000074	PMID:27210743	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:167030	Nephrolithiasis, calcium oxalate		HP:0000007	PMID:27210743	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-19]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001495	PMID:24637309	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0007957	PMID:24637309	PCS		2/5			P	HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000684	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0004322	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0003273	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0003593	OMIM:259600;PMID:24637309;PMID:17059372	PCS		15/16			C	HPO:iea[2009-02-17];HPO:probinson[2020-09-13];HPO:probinson[2022-08-16];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000280	PMID:24637309	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001171	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0008090	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0011463	PMID:24637309	IEA		1/5			C	HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0008011	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0008133	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000316	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0006234	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001763	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001007	PMID:24637309	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0002751	PMID:24637309	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001220	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0025131	OMIM:259600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001783	OMIM:259600;PMID:17059372	PCS		11/11			P	HPO:probinson[2022-08-16];HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0003320	PMID:24637309	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0002829	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000327	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000007	OMIM:259600	IEA					I	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0006466	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000520	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000248	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000446	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001034	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0003016	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001473	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001476	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0003179	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0003493	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001230	PMID:17059372	PCS		1/1			P	HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001072	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000939	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0006252	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000938	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0008078	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001504	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0006012	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000414	PMID:24637309	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0002953	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000212	PMID:24637309	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0002753	PMID:17059372	PCS		1/1			P	HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0003621	OMIM:259600	IEA					C	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001288	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001761	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0005441	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001482	PMID:24637309;PMID:17059372	PCS		2/6			P	HPO:probinson[2022-08-16];HPO:iea[2009-02-17];HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0010537	PMID:24637309	PCS		2/5			P	HPO:probinson[2020-09-13]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0006086	PMID:17059372	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-13];HPO:probinson[2022-08-16]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001239	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001836	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0002007	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0000347	OMIM:259600	IEA					P	HPO:iea[2009-02-17]
OMIM:259600	Multicentric osteolysis, nodulosis, and arthropathy		HP:0001634	PMID:24637309	PCS		1/5			P	HPO:probinson[2020-09-13]
OMIM:604928	Wolfram syndrome 2		HP:0001892	PMID:11317648	PCS					P	HPO:probinson[2013-02-24]
OMIM:604928	Wolfram syndrome 2		HP:0000011	OMIM:604928	IEA					P	HPO:skoehler[2019-09-07]
OMIM:604928	Wolfram syndrome 2		HP:0004313	OMIM:604928	IEA					P	HPO:skoehler[2019-09-07]
OMIM:604928	Wolfram syndrome 2		HP:0003621	PMID:10739754	PCS		11/13			C	HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0004398	PMID:10739754	PCS		11/16			P	HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0000819	PMID:10739754	PCS		16/16			P	HPO:probinson[2013-01-09];HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0000716	PMID:10739754	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0000407	PMID:10739754	PCS		14/16			P	HPO:probinson[2013-02-24];HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0011463	PMID:10739754	PCS		2/13			C	HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0008320	PMID:11317648	PCS					P	HPO:probinson[2013-02-24]
OMIM:604928	Wolfram syndrome 2		HP:0000007	PMID:10739754	PCS					I	HPO:probinson[2013-02-24]
OMIM:604928	Wolfram syndrome 2		HP:0000876	OMIM:604928	IEA					P	HPO:skoehler[2019-09-07]
OMIM:604928	Wolfram syndrome 2		HP:0000648	PMID:10739754	PCS		16/16			P	HPO:probinson[2013-02-24];HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0000873	PMID:10739754	PCS		0/16			P	HPO:probinson[2013-02-24];HPO:probinson[2024-03-10]
OMIM:604928	Wolfram syndrome 2		HP:0001138	OMIM:604928	TAS					P	HPO:skoehler[2015-01-04]
OMIM:604928	Wolfram syndrome 2		HP:0000786	OMIM:604928	IEA					P	HPO:skoehler[2019-09-07]
OMIM:127400	Dyschromatosis symmetrica hereditaria 1		HP:0003593	PMID:12916015	PCS					C	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-15]
OMIM:127400	Dyschromatosis symmetrica hereditaria 1		HP:0007441	PMID:12916015	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-04-15]
OMIM:127400	Dyschromatosis symmetrica hereditaria 1		HP:0000006	PMID:12916015	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-15]
OMIM:310200	Duchenne muscular dystrophy		HP:0001771	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0003115	OMIM:310200	IEA					P	HPO:skoehler[2018-10-08]
OMIM:310200	Duchenne muscular dystrophy		HP:0003236	PMID:29067653	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0001371	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0003551	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0001252	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0011675	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0003391	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0011463	OMIM:310200	TAS		1/1			C	HPO:probinson[2013-03-31];HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0003707	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0003307	OMIM:310200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:310200	Duchenne muscular dystrophy		HP:0002878	OMIM:310200	TAS					P	HPO:skoehler[2014-06-24]
OMIM:310200	Duchenne muscular dystrophy		HP:0002515	PMID:29067653	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0001324	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0001644	OMIM:310200	TAS					P	HPO:skoehler[2012-10-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0001265	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0002870	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0002650	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0002791	OMIM:310200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:310200	Duchenne muscular dystrophy		HP:0003089	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0003560	OMIM:310200	TAS					P	HPO:skoehler[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0002194	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0002091	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0006380	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0001419	PMID:29067653	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0008981	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0001635	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0001638	OMIM:310200	IEA					P	HPO:iea[2009-02-17]
OMIM:310200	Duchenne muscular dystrophy		HP:0002505	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0002747	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:310200	Duchenne muscular dystrophy		HP:0030051	PMID:29067653	PCS		1/1			P	HPO:probinson[2022-05-31]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0000486	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0001252	PMID:37133451	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0012707	PMID:37133451	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0003593	PMID:37133451	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0002181	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0012666	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0012751	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0001508	PMID:37133451	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0011463	PMID:37133451	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0007305	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0003348	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0003623	PMID:37133451	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0002013	PMID:37133451	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0002376	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0011968	PMID:37133451	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0002076	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0001263	PMID:37133451	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0002151	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0012734	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0001081	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0011923	PMID:37133451	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0002928	PMID:37133451	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0001639	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0000546	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0001635	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0000007	PMID:37133451	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0008347	PMID:37133451	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0000741	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0007018	PMID:37133451	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0002104	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620646	Combined oxidative phosphorylation deficiency 59		HP:0003215	PMID:37133451	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0002421	PMID:29576218	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0003676	PMID:29576218	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0000365	OMIM:617954	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0002540	PMID:29576218	PCS		5/5			P	HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001310	PMID:29576218	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001332	PMID:29576218	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001272	PMID:29576218	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001250	PMID:29576218	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001252	PMID:29576218	PCS		4/5			P	HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001251	PMID:29576218	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0003593	PMID:29576218	PCS		4/5			C	HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001508	PMID:29576218	PCS		2/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0011463	PMID:29576218	PCS		1/5			C	HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0007366	PMID:29576218	PCS		1/5			P	HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001249	PMID:29576218	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0000572	PMID:29576218	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001344	PMID:29576218	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0002376	PMID:29576218	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0011968	PMID:29576218	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0002352	OMIM:617954	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001263	PMID:29576218	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0002151	PMID:29576218	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0005484	PMID:29576218	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0000007	PMID:29576218	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0200134	PMID:29576218	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0000648	PMID:29576218	PCS		1/5			P	HPO:probinson[2023-03-12]
OMIM:617954	Multiple mitochondrial dysfunctions syndrome 6		HP:0001257	PMID:29576218	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:255990	Nathalie syndrome		HP:0003202	OMIM:255990	IEA					P	HPO:iea[2009-02-17]
OMIM:255990	Nathalie syndrome		HP:0003115	OMIM:255990	IEA					P	HPO:iea[2009-02-17]
OMIM:255990	Nathalie syndrome		HP:0000365	OMIM:255990	IEA					P	HPO:iea[2009-02-17]
OMIM:255990	Nathalie syndrome		HP:0000518	OMIM:255990	IEA					P	HPO:iea[2009-02-17]
OMIM:255990	Nathalie syndrome		HP:0000007	OMIM:255990	IEA					I	HPO:iea[2009-02-17]
OMIM:255990	Nathalie syndrome		HP:0000119	OMIM:255990	IEA					P	HPO:iea[2009-02-17]
OMIM:255990	Nathalie syndrome		HP:0001510	OMIM:255990	IEA					P	HPO:iea[2009-02-17]
OMIM:608874	Orofacial cleft 5		HP:0000175	PMID:15354328	PCS	HP:0003577				P	HPO:probinson[2013-03-25];HPO:probinson[2020-07-21]
OMIM:608874	Orofacial cleft 5		HP:0000204	PMID:15354328	PCS	HP:0003577				P	HPO:probinson[2013-01-09];HPO:probinson[2020-07-21]
OMIM:608874	Orofacial cleft 5		HP:0000006	PMID:10742093	PCS					I	HPO:probinson[2013-03-25]
OMIM:123100	Craniosynostosis 1		HP:0001650	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0030799	OMIM:123100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:123100	Craniosynostosis 1		HP:0003577	PMID:17343269	PCS		1/2			C	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0001363	OMIM:123100	TAS					P	HPO:probinson[2009-02-17]
OMIM:123100	Craniosynostosis 1		HP:0000263	OMIM:123100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:123100	Craniosynostosis 1		HP:0004422	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0004442	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0000262	OMIM:123100	IEA					P	HPO:probinson[2009-02-17]
OMIM:123100	Craniosynostosis 1		HP:0003593	PMID:17343269	PCS		1/2			C	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0031664	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0011317	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0011220	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0000268	OMIM:123100	TAS					P	HPO:probinson[2009-02-17]
OMIM:123100	Craniosynostosis 1		HP:0002007	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0000006	PMID:17343269	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-08-21]
OMIM:123100	Craniosynostosis 1		HP:0001249	PMID:17343269	PCS		0/2			P	HPO:probinson[2014-05-24];HPO:probinson[2024-03-08]
OMIM:123100	Craniosynostosis 1		HP:0000269	PMID:17343269	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0002136	OMIM:605388	IEA					P	HPO:iea[2009-02-17]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0001272	OMIM:605388	IEA					P	HPO:iea[2009-02-17]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0001260	OMIM:605388	IEA					P	HPO:iea[2009-02-17]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0002075	OMIM:605388	IEA					P	HPO:iea[2009-02-17]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0003593	OMIM:605388	IEA					C	HPO:iea[2009-02-17]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0000007	OMIM:605388	IEA					I	HPO:iea[2009-02-17]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0100021	OMIM:605388	IEA					P	HPO:skoehler[2015-01-27]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0001270	OMIM:605388	IEA					P	HPO:iea[2009-02-17]
OMIM:605388	Cerebral palsy, ataxic, autosomal recessive		HP:0000666	OMIM:605388	IEA					P	HPO:iea[2009-02-17]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0002487	PMID:30982612	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0002069	PMID:30982612	PCS		4/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0002540	PMID:30982612	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0000486	PMID:30982612	PCS		3/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001332	PMID:30982612	PCS		5/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0000463	PMID:30982612	PCS		1/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001250	OMIM:618497	IEA				HP:0031375	P	HPO:skoehler[2019-09-07]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001252	PMID:30982612	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0002020	PMID:30982612	PCS		3/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0003593	PMID:30982612	PCS		4/5			C	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0032794	PMID:30982612	PCS		5/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0000639	PMID:30982612	PCS		2/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0100704	PMID:30982612	PCS		3/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0011463	PMID:30982612	PCS		1/5			C	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0012171	PMID:30982612	PCS		1/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0003763	PMID:30982612	PCS		1/3			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0002059	PMID:30982612	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001344	OMIM:618497	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001883	PMID:30982612	PCS		1/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001266	PMID:30982612	PCS		3/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0002376	PMID:30982612	PCS		5/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0011968	PMID:30982612	PCS		6/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001263	PMID:30982612	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0005484	PMID:30982612	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0011097	PMID:30982612	PCS		4/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0032792	PMID:30982612	PCS		3/6			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0000007	PMID:30982612	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0200134	PMID:30982612	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0000405	PMID:30982612	PCS		1/3			P	HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0002205	PMID:30982612	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:618497	Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements		HP:0001336	PMID:30982612	PCS		6/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-23]
OMIM:126050	Digitotalar dysmorphism		HP:0001838	OMIM:126050	TAS					P	HPO:probinson[2009-02-17]
OMIM:126050	Digitotalar dysmorphism		HP:0100490	OMIM:126050	TAS					P	HPO:probinson[2012-07-26]
OMIM:126050	Digitotalar dysmorphism		HP:0009465	OMIM:126050	TAS					P	HPO:probinson[2009-02-17]
OMIM:126050	Digitotalar dysmorphism		HP:0000006	OMIM:126050	TAS					I	HPO:probinson[2009-02-17]
OMIM:126050	Digitotalar dysmorphism		HP:0003502	OMIM:126050	TAS					P	HPO:probinson[2009-02-17]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000341	PMID:35202563	PCS		2/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0011939	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0004467	PMID:35202563	PCS		3/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000384	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000486	PMID:35202563	PCS		3/6			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0010803	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000365	PMID:35202563	PCS		2/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0002002	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000122	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0100490	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001252	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0003593	PMID:35202563	PCS		3/3			C	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0011318	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001909	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000316	PMID:35202563	PCS		2/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000954	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000238	PMID:35202563	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001822	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0007663	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0002558	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001249	PMID:35202563	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000358	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0002553	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000494	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000054	PMID:35202563	PCS		1/1			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000076	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0002650	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001684	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0011968	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001382	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001263	PMID:35202563	PCS		3/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0004691	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0005280	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0012520	PMID:35202563	PCS		1/2			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001838	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0002808	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000426	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0001852	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000322	PMID:35202563	PCS		2/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000006	PMID:35202563	PCS					I	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000347	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000369	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0000028	PMID:35202563	PCS		1/1			P	HPO:probinson[2022-08-21]
OMIM:619951	Tessadori-van Haaften neurodevelopmental syndrome 4		HP:0002863	PMID:35202563	PCS		1/3			P	HPO:probinson[2022-08-21]
OMIM:300985	Vas deferens, congenital bilateral aplasia of, X-linked		HP:0003251	PMID:27476656	PCS					P	HPO:probinson[2022-10-24]
OMIM:300985	Vas deferens, congenital bilateral aplasia of, X-linked		HP:0011462	PMID:27476656	PCS					C	HPO:probinson[2022-10-24]
OMIM:300985	Vas deferens, congenital bilateral aplasia of, X-linked		HP:0001417	PMID:27476656	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-24]
OMIM:300985	Vas deferens, congenital bilateral aplasia of, X-linked		HP:0012873	PMID:27476656	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-24]
OMIM:300985	Vas deferens, congenital bilateral aplasia of, X-linked		HP:0000027	PMID:27476656	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-24]
OMIM:619789	Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive		HP:0005532	PMID:34818416	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:619789	Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive		HP:0011463	PMID:34818416	PCS		1/1			C	HPO:probinson[2022-05-29]
OMIM:619789	Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive		HP:0000007	PMID:34818416	PCS					I	HPO:probinson[2022-05-29]
OMIM:619789	Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive		HP:0001972	PMID:34818416	PCS		1/1			P	HPO:probinson[2022-05-29]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001891	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003453	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0000123	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0000100	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003454	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003496	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003493	PMID:16446975	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001890	PMID:10412980	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0025300	OMIM:603909	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002240	PMID:10412980	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001904	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002716	PMID:10412980	PCS	HP:0003593	1/1			P	HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002239	PMID:16446975	PCS					P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002731	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001744	PMID:10412980	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0005404	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002853	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002633	OMIM:603909	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003565	PMID:10412980	PCS		1/1			P	HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002730	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002851	PMID:10412980	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001880	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003621	OMIM:603909	IEA					C	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002972	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001025	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003262	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003261	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002729	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0000967	PMID:16446975	IEA					P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0002923	PMID:10412980	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003613	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001973	OMIM:603909	IEA					P	HPO:iea[2009-02-17]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0001873	PMID:16446975	PCS					P	HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0000006	PMID:10412980	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0004844	OMIM:603909;PMID:16446975	PCS		20/20			P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13];HPO:probinson[2020-10-13]
OMIM:603909	Autoimmune lymphoproliferative syndrome, type IIA		HP:0003237	PMID:16446975	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-10-13]
OMIM:207740	Aplasia of extensor muscles of fingers, unilateral, with generalizedpolyneuropathy		HP:0003011	OMIM:207740	IEA					P	HPO:iea[2009-02-17]
OMIM:207740	Aplasia of extensor muscles of fingers, unilateral, with generalizedpolyneuropathy		HP:0001271	OMIM:207740	IEA					P	HPO:iea[2009-02-17]
OMIM:207740	Aplasia of extensor muscles of fingers, unilateral, with generalizedpolyneuropathy		HP:0000007	OMIM:207740	IEA					I	HPO:iea[2009-02-17]
OMIM:207740	Aplasia of extensor muscles of fingers, unilateral, with generalizedpolyneuropathy		HP:0000966	OMIM:207740	IEA					P	HPO:iea[2009-02-17]
OMIM:155900	Melkersson-Rosenthal syndrome		HP:0010628	OMIM:155900	IEA					P	HPO:skoehler[2010-06-20]
OMIM:155900	Melkersson-Rosenthal syndrome		HP:0000221	OMIM:155900	IEA					P	HPO:iea[2009-02-17]
OMIM:155900	Melkersson-Rosenthal syndrome		HP:0000282	OMIM:155900	IEA					P	HPO:iea[2009-02-17]
OMIM:155900	Melkersson-Rosenthal syndrome		HP:0000006	OMIM:155900	IEA					I	HPO:iea[2009-02-17]
OMIM:155900	Melkersson-Rosenthal syndrome		HP:0000478	OMIM:155900	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0002025	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000286	PMID:7545870	PCS		2/11			P	HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0002961	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0008209	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000340	PMID:22373003;PMID:7545870	PCS		21/21			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31];HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0000582	PMID:7545870	PCS		11/11			P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0003577	PMID:22373003	PCS					C	HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0007814	PMID:7545870	PCS		2/11			P	HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0002023	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000265	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0004322	OMIM:251260	TAS					P	HPO:skoehler[2013-02-27]
OMIM:251260	Nijmegen breakage syndrome		HP:0002002	PMID:7545870	PCS		2/11			P	HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0001890	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0010620	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0002180	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000957	PMID:22373003	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0002837	PMID:7545870	PCS		6/11			P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0002859	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0006532	PMID:7545870	PCS		6/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0000752	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0001249	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0005602	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0002014	OMIM:251260	TAS					P	HPO:skoehler[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0004798	OMIM:251260	TAS					P	HPO:skoehler[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0005403	OMIM:251260	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000175	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000252	PMID:7545870	PCS	HP:0003577	11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12];HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0000010	PMID:7545870	PCS		3/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0000453	PMID:22373003	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0003189	PMID:22373003	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0000750	PMID:22373003	PCS					P	HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0002110	PMID:7545870	PCS		2/11			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0004691	PMID:7545870	PCS		5/11			P	HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0010976	OMIM:251260	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000007	PMID:22373003	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0000524	PMID:7545870	PCS		5/11			P	HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0000403	PMID:7545870	PCS		2/11			P	HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0009733	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0001511	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000400	PMID:7545870	PCS		11/11			P	HPO:probinson[2013-08-11];HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0000246	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0001852	PMID:7545870	PCS		7/11			P	HPO:probinson[2023-03-31]
OMIM:251260	Nijmegen breakage syndrome		HP:0001873	OMIM:251260	IEA					P	HPO:skoehler[2010-06-20]
OMIM:251260	Nijmegen breakage syndrome		HP:0000204	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0002665	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0002885	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:251260	Nijmegen breakage syndrome		HP:0000347	PMID:7545870	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-12]
OMIM:251260	Nijmegen breakage syndrome		HP:0000126	OMIM:251260	IEA					P	HPO:iea[2009-02-17]
OMIM:186580	Blau syndrome		HP:0007813	OMIM:186580	IEA					P	HPO:iea[2009-02-17]
OMIM:186580	Blau syndrome		HP:0001386	PMID:4056967	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0025230	OMIM:186580	TAS					P	HPO:skoehler[2017-07-13]
OMIM:186580	Blau syndrome		HP:0005830	OMIM:186580	IEA					P	HPO:skoehler[2010-06-18]
OMIM:186580	Blau syndrome		HP:0000585	OMIM:186580	IEA					P	HPO:skoehler[2010-06-18]
OMIM:186580	Blau syndrome		HP:0001101	PMID:4056967	PCS		3/11			P	HPO:skoehler[2010-06-18];HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0100490	PMID:11528384;OMIM:186580	PCS		17/20			P	HPO:probinson[2012-06-04];HPO:probinson[2020-11-28];HPO:iea[2009-02-17]
OMIM:186580	Blau syndrome		HP:0012219	PMID:19479837	PCS		3/45			P	HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0001291	OMIM:186580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:186580	Blau syndrome		HP:0011505	OMIM:186580	TAS					P	HPO:probinson[2012-06-04]
OMIM:186580	Blau syndrome		HP:0100769	PMID:19479837	PCS					P	HPO:probinson[2012-06-04];HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0000518	OMIM:186580	IEA					P	HPO:skoehler[2010-06-18]
OMIM:186580	Blau syndrome		HP:0000822	PMID:19479837	PCS		4/45			P	HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0001701	PMID:19479837	PCS		2/45			P	HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0007432	PMID:19479837	PCS		42/44			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0000964	OMIM:186580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:186580	Blau syndrome		HP:0000554	PMID:19479837;PMID:11528384	PCS		39/54			P	HPO:probinson[2012-06-04];HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:186580	Blau syndrome		HP:0000598	OMIM:186580	IEA					P	HPO:iea[2009-02-17]
OMIM:186580	Blau syndrome		HP:0200042	OMIM:186580	IEA					P	HPO:skoehler[2010-06-20]
OMIM:186580	Blau syndrome		HP:0000501	OMIM:186580	IEA					P	HPO:skoehler[2010-06-18]
OMIM:186580	Blau syndrome		HP:0000006	OMIM:186580	TAS					I	HPO:probinson[2009-02-17]
OMIM:186580	Blau syndrome		HP:0001369	PMID:19479837;PMID:11528384;PMID:4056967	PCS		61/66			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0000473	OMIM:118800	TAS					P	HPO:probinson[2012-04-27]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0002015	OMIM:118800	IEA					P	HPO:iea[2009-02-17]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0002411	OMIM:118800	IEA					P	HPO:iea[2009-02-17]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0002268	OMIM:118800	IEA					P	HPO:iea[2009-02-17]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0001260	OMIM:118800	IEA					P	HPO:iea[2009-02-17]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0011463	PMID:15262732	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0007098	PMID:15262732	PCS		12/12			P	HPO:probinson[2012-04-27];HPO:probinson[2022-12-22]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0000273	OMIM:118800	IEA					P	HPO:iea[2009-02-17]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0003593	OMIM:118800	TAS					C	HPO:skoehler[2012-11-16]
OMIM:118800	Paroxysmal nonkinesigenic dyskinesia 1		HP:0000006	PMID:15262732	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-22]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000286	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001331	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0003312	PMID:20301362	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001177	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002389	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000486	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002144	OMIM:194190	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0004322	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs;ISBN-13:978-3-7945-2657-4	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0003199	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0004484	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002020	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001290	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001171	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040283			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000639	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000316	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000558	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000954	OMIM:194190	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000238	OMIM:194190	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0008850	ISBN-13:978-3-7945-2657-4	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000119	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		25%			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001841	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0003745	OMIM:194190	TAS					I	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001840	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002974	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002553	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0007109	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000252	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001385	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000175	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002353	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		90%			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002750	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001263	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000407	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		15%			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002948	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002827	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001812	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000405	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		40%			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000202	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000444	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000047	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		50%			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000322	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000960	OMIM:194190	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000520	ISBN-13:978-3-7945-2657-4	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0009778	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000402	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000006	OMIM:194190	TAS					I	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000204	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000384	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0004467	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000188	OMIM:194190	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0010109	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0009918	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002162	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001274	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001508	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs;ISBN-13:978-3-7945-2657-4	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001629	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0007385	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040283			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000612	ISBN-13:978-3-7945-2657-4	TAS		30%			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0030680	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000733	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002119	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001747	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002714	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0006655	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000377	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001028	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000431	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002650	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001762	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002057	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0004794	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002011	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		33%			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000151	OMIM:194190	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001080	OMIM:194190	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0009193	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0011863	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000826	OMIM:194190	TAS					P	HPO:skoehler[2012-10-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000902	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001518	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002808	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000508	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000668	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000348	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001558	OMIM:194190	TAS					P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001511	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs;ISBN-13:978-3-7945-2657-4	TAS		HP:0040281			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000465	OMIM:194190	TAS		HP:0040283			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001510	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs;ISBN-13:978-3-7945-2657-4	TAS		HP:0040281			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0001631	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		27%			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000347	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0000028	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		50%			P	HPO:iea[2010-09-10]
OMIM:194190	Wolf-Hirschhorn syndrome		HP:0002721	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		69%			P	HPO:iea[2010-09-10]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000286	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0004325	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000486	OMIM:300749	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000365	OMIM:300749	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0004322	PMID:19165920	PCS		3/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001250	PMID:19165920	PCS		3/6			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000480	PMID:19165920	PCS		1/6			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0003196	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001252	PMID:19165920	PCS		3/5			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001090	OMIM:300749	TAS					P	HPO:skoehler[2015-07-26]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0012110	PMID:19165920	PCS		5/5			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000639	OMIM:300749	TAS		HP:0040283			P	HPO:skoehler[2015-07-26]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000319	PMID:19165920	PCS		1/5			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000316	PMID:19165920	PCS		1/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0008897	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0025336	PMID:19165920	PCS		3/4			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001324	OMIM:300749	TAS					P	HPO:skoehler[2015-07-26]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0004879	PMID:19165920	PCS		1/6			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000253	OMIM:300749	TAS					P	HPO:skoehler[2015-12-30]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000252	PMID:19165920	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000494	PMID:19165920	PCS		1/5			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001344	PMID:19165920	PCS		4/4			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0011968	PMID:19165920	PCS		5/5			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0002198	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001263	PMID:19165920	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000609	PMID:19165920	PCS		1/6			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000407	PMID:19165920	PCS		2/4			P	HPO:skoehler[2012-11-21];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000966	OMIM:300749	TAS					P	HPO:skoehler[2015-07-26]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000400	PMID:19165920	PCS		3/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001257	PMID:19165920	PCS		2/6			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001276	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000343	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0002365	PMID:19165920	PCS		5/5			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000218	OMIM:300749	TAS					P	HPO:skoehler[2015-07-26]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001423	PMID:19165920	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001302	OMIM:300749	TAS		HP:0040283			P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000455	PMID:19165920	PCS		2/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001347	OMIM:300749	TAS					P	HPO:skoehler[2015-07-26]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0008936	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000431	PMID:19165920	PCS		3/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0002650	PMID:19165920	PCS		2/6			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001321	PMID:19165920	PCS		5/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0031936	PMID:19165920	PCS		3/3			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000426	OMIM:300749	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000543	PMID:19165920	PCS		2/6			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0001357	PMID:19165920	PCS		1/5			P	HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000300	OMIM:300749	TAS					P	HPO:skoehler[2015-07-26]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0000347	PMID:19165920	PCS		3/5			P	HPO:skoehler[2012-10-14];HPO:probinson[2021-09-06]
OMIM:300749	Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia		HP:0009879	PMID:19165920	PCS		5/5			P	HPO:probinson[2021-09-06]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0001696	PMID:28041644	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0002110	PMID:28041644	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0001419	PMID:28041644	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0003251	PMID:28041644	PCS		1/1			P	HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0033036	PMID:28041644	PCS		4/4			P	HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0012735	PMID:28041644	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0002205	PMID:28041644	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0000389	PMID:28041644	PCS		4/4			P	HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0001742	PMID:28041644	PCS		4/4			P	HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0011108	PMID:28041644	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0002643	PMID:28041644	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:300991	Ciliary dyskinesia, primary, 36, X-linked		HP:0003623	PMID:28041644	PCS		2/2			C	HPO:probinson[2022-12-19]
OMIM:120435	Lynch syndrome I		HP:0003003	OMIM:120435	TAS					P	HPO:probinson[2009-02-17]
OMIM:120435	Lynch syndrome I		HP:0000006	OMIM:120435	TAS					I	HPO:skoehler[2009-02-17]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0000340	PMID:27737959	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-19]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0003577	PMID:27737959	PCS		1/1			C	HPO:probinson[2022-12-19]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0001344	PMID:27737959	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-19]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0004322	PMID:27737959	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-19]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0001518	PMID:27737959	PCS		1/1			P	HPO:probinson[2022-12-19]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0000729	PMID:27737959	PCS		1/1			P	HPO:probinson[2022-12-19]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0011451	PMID:27737959	PCS		1/1			P	HPO:probinson[2022-12-19]
OMIM:617983	Microcephaly 21, primary, autosomal recessive		HP:0000007	PMID:27737959	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-12-19]
OMIM:616445	Candidiasis, familial, 9		HP:0011463	PMID:25918342	PCS		1/3			C	HPO:probinson[2022-09-08]
OMIM:616445	Candidiasis, familial, 9		HP:0033351	PMID:25918342	PCS		1/3			P	HPO:probinson[2022-09-08];HPO:probinson[2022-09-08]
OMIM:616445	Candidiasis, familial, 9		HP:0002728	PMID:25918342	PCS		3/3			P	HPO:probinson[2022-09-08]
OMIM:616445	Candidiasis, familial, 9		HP:0003593	PMID:25918342	PCS		2/3			C	HPO:probinson[2022-09-08]
OMIM:616445	Candidiasis, familial, 9		HP:0000007	PMID:25918342	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-08]
OMIM:616445	Candidiasis, familial, 9		HP:0012203	PMID:25918342	PCS		1/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-09-08]
OMIM:616445	Candidiasis, familial, 9		HP:0011107	PMID:25918342	PCS		1/3			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-09-08]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0008936	PMID:31031012	PCS		11/11			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0000252	PMID:31031012	PCS		6/11			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0002059	PMID:31031012	PCS		3/10			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0001344	PMID:31031012	PCS		8/8			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0002540	PMID:31031012	PCS		7/8			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0002188	PMID:31031012	PCS		1/12			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0002079	PMID:31031012	PCS		6/10			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0001250	PMID:31031012	PCS	HP:0003593	11/11			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0001272	PMID:31031012	PCS		1/10			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0030891	PMID:31031012	PCS		2/11			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0002061	PMID:31031012	PCS					P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0010841	PMID:31031012	PCS		7/9			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0011344	PMID:31031012	PCS					P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0003819	PMID:31031012	PCS		3/11			C	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0000007	PMID:31031012	PCS					I	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0008872	PMID:31031012	PCS		9/11			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0001249	PMID:31031012	PCS		11/11			P	HPO:probinson[2020-05-15]
OMIM:618468	Epileptic encephalopathy, early infantile, 76		HP:0006986	PMID:31031012	PCS					P	HPO:probinson[2020-05-15]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001397	PMID:11479539	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0003577	OMIM:269700	IEA					C	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000065	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001176	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000144	OMIM:269700	TAS			FEMALE		P	HPO:skoehler[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001394	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0002240	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0003292	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0003809	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000877	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0009125	OMIM:269700	TAS					P	HPO:skoehler[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000956	PMID:11479539	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001544	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0040217	PMID:11479539	PCS		4/4			P	HPO:probinson[2022-09-04]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0002833	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0002910	OMIM:269700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001620	OMIM:269700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001007	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001744	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000098	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0002155	PMID:11479539	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0002591	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0005144	OMIM:269700	TAS					P	HPO:lccarmody[2018-12-28]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001639	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001735	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0003716	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001537	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000007	PMID:11479539	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0001833	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000868	OMIM:269700	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0025128	OMIM:269700	TAS					P	HP:probinson[2019-01-22]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0003758	OMIM:269700	TAS					P	HP:probinson[2019-01-22]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0003758	PMID:11479539	PCS	HP:0003577	4/4			P	HPO:probinson[2022-09-04]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0008665	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0005616	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000400	OMIM:269700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000147	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0005978	PMID:11479539	PCS		3/4			P	HPO:probinson[2022-09-04]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000842	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000303	OMIM:269700	IEA					P	HPO:iea[2009-02-17]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000787	OMIM:269700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:269700	Lipodystrophy, congenital generalized, type 2		HP:0000325	OMIM:269700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601887	Malignant hyperthermia, susceptibility to, 5		HP:0002047	PMID:9199552	PCS					P	HPO:probinson[2023-05-19]
OMIM:601887	Malignant hyperthermia, susceptibility to, 5		HP:0012416	OMIM:601887	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601887	Malignant hyperthermia, susceptibility to, 5		HP:0001649	OMIM:601887	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601887	Malignant hyperthermia, susceptibility to, 5		HP:0001945	OMIM:601887	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601887	Malignant hyperthermia, susceptibility to, 5		HP:0000006	PMID:9199552	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-19]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0002015	PMID:16916845	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0010628	PMID:16916845	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0003750	PMID:16916845	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0011968	PMID:16916845	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0002033	PMID:16916845	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0001252	PMID:16916845	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0001270	PMID:16916845	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0002093	PMID:16916845	PCS		1/1		HP:0025303	P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0030319	PMID:16916845	PCS		1/1			P	HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0030208	PMID:16916845	PCS		0/1			P	HPO:probinson[2022-10-24];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0000508	PMID:16916845	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0000007	PMID:16916845	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0000218	PMID:16916845	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-10-24]
OMIM:616323	Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency		HP:0003623	PMID:16916845	PCS		1/1			C	HPO:probinson[2022-10-24]
OMIM:620849	Spermatogenic failure 93		HP:0033393	PMID:34155512	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0034011	PMID:34155512	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0032560	PMID:34155512	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0003251	PMID:34155512	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0011462	PMID:34155512	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0012207	PMID:34155512	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0000007	PMID:34155512	PCS					I	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0034811	PMID:34155512	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0000798	PMID:34155512	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0032558	PMID:34155512	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:620849	Spermatogenic failure 93		HP:0032559	PMID:34155512	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-14]
OMIM:619004	Deeah syndrome		HP:0004325	PMID:32761064	PCS		10/13			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000286	PMID:32761064	PCS		1/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000365	PMID:32761064	PCS		4/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000486	PMID:32761064	PCS		2/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002188	PMID:32761064	PCS		1/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002024	PMID:32761064	PCS		2/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0004322	PMID:32761064	PCS		14/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001250	PMID:32761064	PCS		9/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000160	PMID:32761064	PCS		10/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001252	PMID:32761064	PCS		14/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0003196	PMID:32761064	PCS		3/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0012745	PMID:32761064	PCS		2/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0031861	PMID:32761064	PCS		3/11			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001522	PMID:32761064	PCS		1/14			C	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000278	PMID:32761064	PCS		2/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0007328	PMID:32761064	PCS		9/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000054	PMID:32761064	PCS		4/5	MALE		P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002353	PMID:32761064	PCS		9/13			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002750	PMID:32761064	PCS		2/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0003320	PMID:32761064	PCS		1/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0004370	PMID:32761064	PCS					P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0010557	PMID:32761064	PCS		3/14			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001738	PMID:32761064	PCS		13/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0032210	PMID:32761064	PCS		2/13			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000007	PMID:32761064	PCS					I	HPO:probinson[2020-11-30];HPO:probinson[2022-12-03]
OMIM:619004	Deeah syndrome		HP:0000966	PMID:32761064	PCS		6/11			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000565	PMID:32761064	PCS		4/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000322	PMID:32761064	PCS		2/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000369	PMID:32761064	PCS		3/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000522	PMID:32761064	PCS		5/13			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002028	PMID:32761064	PCS		10/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000341	PMID:32761064	PCS		2/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000343	PMID:32761064	PCS		1/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000189	PMID:32761064	PCS		2/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0010627	PMID:32761064	PCS		2/13			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000540	PMID:32761064	PCS		1/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002162	PMID:32761064	PCS		1/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002240	PMID:32761064	PCS		4/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0005274	PMID:32761064	PCS		1/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001270	PMID:32761064	PCS		14/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0025481	PMID:32761064	PCS		1/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0033078	PMID:32761064	PCS		3/13			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0012450	PMID:32761064	PCS		6/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000218	PMID:32761064	PCS		4/12			P	HPO:probinson[2020-12-03];HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0006610	PMID:32761064	PCS		1/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002015	PMID:32761064	PCS		2/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001561	PMID:32761064	PCS	HP:0011461	1/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0020062	PMID:32761064	PCS		13/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000750	PMID:32761064	PCS		9/11			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000871	PMID:32761064	PCS		8/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002650	PMID:32761064	PCS		1/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000470	PMID:32761064	PCS		2/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0011421	PMID:32761064	PCS		1/14			C	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0011344	PMID:32761064	PCS		14/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0012510	PMID:32761064	PCS		4/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0003819	PMID:32761064	PCS		5/14			C	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001998	PMID:32761064	PCS	HP:0003623	9/13			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000348	PMID:32761064	PCS		4/12			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000824	PMID:32761064	PCS		8/10			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001319	PMID:32761064	PCS	HP:0003623	4/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001511	PMID:32761064	PCS		3/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0001873	PMID:32761064	PCS		5/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000028	PMID:32761064	PCS		4/5	MALE		P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000545	PMID:32761064	PCS		1/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0002643	PMID:32761064	PCS	HP:0003623	7/14			P	HPO:probinson[2020-12-03]
OMIM:619004	Deeah syndrome		HP:0000742	PMID:32761064	PCS		6/11			P	HPO:probinson[2020-12-03]
OMIM:108420	Spermatogenic failure 2		HP:0030346	PMID:33437391	PCS		0/1			P	HPO:probinson[2022-08-04]
OMIM:108420	Spermatogenic failure 2		HP:0030345	PMID:33437391	PCS		0/1			P	HPO:probinson[2022-08-04]
OMIM:108420	Spermatogenic failure 2		HP:0003251	PMID:33437391	PCS		1/1			P	HPO:probinson[2022-08-04]
OMIM:108420	Spermatogenic failure 2		HP:0011462	PMID:33437391	PCS		1/1			C	HPO:probinson[2022-08-04]
OMIM:108420	Spermatogenic failure 2		HP:0030087	PMID:33437391	PCS		0/1			P	HPO:probinson[2022-08-04]
OMIM:108420	Spermatogenic failure 2		HP:0000007	PMID:33437391	PCS					I	HPO:probinson[2022-08-04]
OMIM:108420	Spermatogenic failure 2		HP:0011961	PMID:33437391	PCS		1/1			P	HPO:probinson[2022-08-04]
OMIM:108420	Spermatogenic failure 2		HP:0000798	OMIM:108420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:108420	Spermatogenic failure 2		HP:0000027	OMIM:108420	TAS					P	HPO:skoehler[2017-07-13]
OMIM:602342	Pierpont syndrome		HP:0004325	PMID:26769062	PCS		3/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0002265	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0001773	OMIM:602342	TAS					P	HPO:skoehler[2013-04-08]
OMIM:602342	Pierpont syndrome		HP:0000486	OMIM:602342	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000365	PMID:26769062	PCS		5/5			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0001212	PMID:26769062	IEA		6/6			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0004322	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0001250	OMIM:602342	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0003196	OMIM:602342	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602342	Pierpont syndrome		HP:0000482	PMID:26769062	PCS		3/6			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0001252	PMID:26769062	PCS		6/6			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000283	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0006191	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0009381	PMID:26769062	PCS		6/6			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000759	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000319	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0011341	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000316	OMIM:602342	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602342	Pierpont syndrome		HP:0001769	OMIM:602342	TAS					P	HPO:skoehler[2013-04-08]
OMIM:602342	Pierpont syndrome		HP:0001169	OMIM:602342	TAS					P	HPO:probinson[2013-04-07]
OMIM:602342	Pierpont syndrome		HP:0000358	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0001249	PMID:26769062	PCS		6/6			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000252	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000054	OMIM:602342	TAS		HP:0040283	MALE		P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0007946	OMIM:602342	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602342	Pierpont syndrome		HP:0011968	OMIM:602342	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000293	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000490	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0001263	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0011800	OMIM:602342	TAS					P	HPO:skoehler[2013-11-28]
OMIM:602342	Pierpont syndrome		HP:0100853	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0009890	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0002708	OMIM:602342	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0002308	PMID:30365874	PCS		1/2			P	HP:probinson[2019-01-21];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000568	OMIM:602342	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602342	Pierpont syndrome		HP:0000289	OMIM:602342	TAS					P	HPO:skoehler[2012-10-17]
OMIM:602342	Pierpont syndrome		HP:0000006	PMID:26769062	PCS					I	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000248	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000687	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000445	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0001276	OMIM:602342	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000581	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0001508	OMIM:602342	TAS		HP:0040283			P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0001869	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0006610	OMIM:602342;PMID:21834056	PCS		14/15			P	HP:probinson[2019-01-21];HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000455	PMID:26769062	PCS		6/6			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000750	PMID:21834056	PCS		9/9			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0002650	PMID:26769062	PCS		5/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0004279	OMIM:602342	TAS					P	HPO:probinson[2013-04-07]
OMIM:602342	Pierpont syndrome		HP:0000233	PMID:26769062	PCS		6/6			P	HPO:skoehler[2018-10-08];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000232	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000272	PMID:26769062	PCS		6/6			P	HPO:skoehler[2012-10-16];HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000470	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0045025	PMID:26769062	PCS		5/6			P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0000506	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0012043	OMIM:602342	IEA					P	HPO:skoehler[2018-10-08]
OMIM:602342	Pierpont syndrome		HP:0032276	PMID:26769062	PCS					P	HP:probinson[2019-02-12]
OMIM:602342	Pierpont syndrome		HP:0000348	OMIM:602342	TAS					P	HPO:skoehler[2012-10-16]
OMIM:602342	Pierpont syndrome		HP:0000028	PMID:28562391	PCS	HP:0003577	1/1	MALE		P	HP:probinson[2019-01-21]
OMIM:602342	Pierpont syndrome		HP:0001831	PMID:26769062	PCS		6/6			P	HP:probinson[2019-01-21]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001792	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001520	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0003355	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001250	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001263	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001252	OMIM:614520	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0012448	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2013-11-28]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001290	OMIM:614520	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0005280	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0002919	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001508	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001903	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0011220	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001537	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0000316	OMIM:614520	TAS				HP:0012825	P	HPO:skoehler[2013-06-06]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0000218	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0006610	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0005528	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0003745	OMIM:614520	TAS					I	HPO:skoehler[2015-12-30]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001159	OMIM:614520	IEA					P	HPO:skoehler[2019-09-07]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001873	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0002126	OMIM:614520	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0001875	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614520	Encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency		HP:0003128	OMIM:614520	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0031956	PMID:12709789	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0011924	PMID:12709789	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0002151	PMID:12709789	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0002240	PMID:12709789	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0003593	PMID:12709789	PCS		1/1			C	HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0000007	PMID:12709789	PCS					I	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0001943	PMID:12709789	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0020078	PMID:12709789	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0012759	PMID:12709789	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0001942	PMID:12709789	PCS		1/1			P	HPO:skoehler[2013-10-06];HPO:probinson[2023-02-19]
OMIM:615158	Mitochondrial complex III deficiency, nuclear type 3		HP:0031964	PMID:12709789	PCS		1/1			P	HPO:probinson[2023-02-19]
OMIM:113000	Brachydactyly, type B1		HP:0003026	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0000054	PMID:10986040	PCS			MALE		P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0005831	OMIM:113000	TAS					P	HPO:skoehler[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0000260	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0000270	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0010554	OMIM:113000	PCS	HP:0003577	HP:0040283			P	HPO:skoehler[2013-06-23]
OMIM:113000	Brachydactyly, type B1		HP:0004590	PMID:19461659	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0011304	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0012385	PMID:10986040	PCS					P	HPO:skoehler[2013-10-22]
OMIM:113000	Brachydactyly, type B1		HP:0001629	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0009473	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0001804	PMID:9973295	PCS					P	HPO:probinson[2017-12-17]
OMIM:113000	Brachydactyly, type B1		HP:0002937	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0002948	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0005819	PMID:9973295	PCS					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0010185	PMID:9973295	PCS					P	HPO:probinson[2017-12-17]
OMIM:113000	Brachydactyly, type B1		HP:0002944	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0001159	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0000696	OMIM:113000	IEA					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0000006	PMID:10986040	PCS					I	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0001798	OMIM:113000	PCS					P	HPO:iea[2009-02-17]
OMIM:113000	Brachydactyly, type B1		HP:0009835	PMID:10986040	PCS		HP:0040281			P	HP:probinson[2018-07-06];HP:probinson[2018-07-14]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0003477	OMIM:616451	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0003621	PMID:25609768	PCS					C	HPO:probinson[2023-01-28]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0003487	OMIM:616451	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0001123	OMIM:616451	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0001284	OMIM:616451	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0000007	PMID:25609768	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-28]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0002936	OMIM:616451	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0000648	OMIM:616451	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0000505	OMIM:616451	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0001258	OMIM:616451	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0003677	OMIM:616451	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616451	Spastic paraplegia 74, autosomal recessive		HP:0001347	OMIM:616451	IEA					P	HPO:skoehler[2018-10-08]
OMIM:619762	Kury-Isidor syndrome		HP:0000483	PMID:35051358	PCS		2/11			P	HPO:probinson[2022-04-17];HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0010804	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0003577	PMID:35051358	PCS		11/11			C	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000486	PMID:35051358	PCS		3/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000343	PMID:35051358	PCS		4/11			P	HPO:probinson[2022-04-17];HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001596	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001156	PMID:35051358	PCS		2/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000463	PMID:35051358	PCS		2/22			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001250	PMID:35051358	PCS		6/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001252	PMID:35051358	PCS		7/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001270	PMID:35051358	PCS		6/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000280	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001629	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000998	PMID:35051358	PCS		3/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0009623	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000218	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001249	PMID:35051358	PCS					P	HPO:probinson[2022-04-17];HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001385	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000494	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000750	PMID:35051358	PCS		11/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001762	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0002650	PMID:35051358	PCS		2/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0011968	PMID:35051358	PCS		4/8			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000490	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001263	PMID:35051358	PCS		11/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000470	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0011003	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001838	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000729	PMID:35051358	PCS		2/10			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000508	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000403	PMID:35051358	PCS		4/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0006101	PMID:35051358	PCS		3/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000207	PMID:35051358	PCS		2/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0030490	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0002007	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0001510	PMID:35051358	PCS		9/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0007018	PMID:35051358	PCS		3/10			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000960	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000006	PMID:35051358	PCS					I	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000369	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000248	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000126	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:619762	Kury-Isidor syndrome		HP:0000687	PMID:35051358	PCS		1/11			P	HPO:probinson[2022-04-17]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0002014	PMID:10525050	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0004432	PMID:10525050	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0002783	PMID:11920841	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0003593	PMID:11920841	PCS		1/1			C	HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0410293	PMID:10525050	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0001508	PMID:10525050	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0002718	PMID:11920841	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0030252	PMID:11920841	PCS		1/1			P	HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0000007	PMID:10525050	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0000403	PMID:11920841	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0002837	PMID:10525050	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0002843	PMID:11920841	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0001875	PMID:10525050	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-02-21]
OMIM:613501	Agammaglobulinemia 3, autosomal recessive		HP:0003623	PMID:10525050	PCS		1/1			C	HPO:probinson[2023-02-21]
OMIM:615170	Wahab syndrome		HP:0012385	OMIM:615170	IEA					P	HPO:skoehler[2015-08-05]
OMIM:615170	Wahab syndrome		HP:0001773	OMIM:615170	TAS					P	HPO:skoehler[2013-04-18]
OMIM:615170	Wahab syndrome		HP:0004279	OMIM:615170	TAS					P	HPO:skoehler[2013-04-18]
OMIM:615170	Wahab syndrome		HP:0010049	OMIM:615170	TAS					P	HPO:skoehler[2013-05-31]
OMIM:615170	Wahab syndrome		HP:0031013	OMIM:615170	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615170	Wahab syndrome		HP:0001181	OMIM:615170	TAS					P	HPO:skoehler[2013-04-18]
OMIM:615170	Wahab syndrome		HP:0030084	OMIM:615170	IEA					P	HPO:skoehler[2015-08-05]
OMIM:615170	Wahab syndrome		HP:0001159	OMIM:615170	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:615170	Wahab syndrome		HP:0009778	OMIM:615170	TAS					P	HPO:skoehler[2013-04-18]
OMIM:615170	Wahab syndrome		HP:0000006	OMIM:615170	TAS					I	HPO:skoehler[2013-04-18]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0000175	PMID:24942156	PCS		2/2			P	HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0003577	PMID:24942156	PCS		2/2			C	HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0000494	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0011904	PMID:24942156	PCS		2/2			P	HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0011800	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0012741	PMID:24942156	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0001419	PMID:24942156	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0008551	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0000405	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0005518	PMID:24942156	PCS		2/2			P	HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0030270	PMID:24942156	PCS					P	HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0000653	PMID:24942156	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0001972	PMID:24942156	PCS		1/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0000413	PMID:24942156	PCS		1/2			P	HPO:probinson[2022-12-20]
OMIM:300946	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis		HP:0000347	PMID:24942156	PCS		2/2			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-12-20]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002169	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003236	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003676	PMID:26094573	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003596	PMID:26094573	PCS		2/4			C	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001310	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001272	PMID:26094573	PCS		2/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002120	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003394	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001251	OMIM:616479	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0011712	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0100543	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0007340	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0007220	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0007366	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0007663	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002317	PMID:26094573	PCS		4/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003327	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001324	PMID:26094573	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001488	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0000597	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001348	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003688	PMID:26094573	PCS		3/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003546	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001347	OMIM:616479	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003326	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001265	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003202	OMIM:616479	TAS					P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002136	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002015	PMID:26094573	PCS		4/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003200	PMID:26094573	PCS		3/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0003487	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001288	PMID:26094573	PCS		2/8			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0000590	PMID:26094573	PCS		4/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001260	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002151	PMID:26094573	PCS		2/4			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002172	PMID:26094573	PCS		1/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002093	OMIM:616479	TAS		HP:0040283			P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0025709	PMID:26094573	PCS		2/4			C	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0001618	PMID:26094573	PCS		2/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0000508	PMID:26094573	PCS		2/4			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0000602	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0009830	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0007256	OMIM:616479	TAS					P	HPO:skoehler[2015-08-02]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0000007	PMID:26094573	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002505	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:616479	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2		HP:0002403	PMID:26094573	PCS		1/4			P	HPO:probinson[2023-03-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000286	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002465	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002188	PMID:30827496	PCS		1/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000365	PMID:30827496	PCS		3/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001773	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000046	PMID:30827496;OMIM:618454	PCS		11/16			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000089	PMID:30827496	PCS		4/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0004322	PMID:30827496	PCS		7/23			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001250	PMID:30827496	PCS		4/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001252	PMID:30827496	PCS		8/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0003196	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0410030	PMID:30827496	PCS	HP:0003577	5/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0011463	PMID:30424743	PCS		1/1			C	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000319	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0011220	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000316	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0007366	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0030260	PMID:30827496	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001643	PMID:30827496	PCS		3/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001249	PMID:30827496	PCS		17/20			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000358	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002553	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000175	PMID:30827496	PCS		5/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000252	PMID:30827496	PCS		7/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001344	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002079	PMID:30827496	PCS		1/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0011968	PMID:30827496	PCS		8/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002395	PMID:30827496	PCS		5/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000490	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001263	PMID:30827496	PCS		24/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002194	PMID:30424743	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000729	PMID:30424743;PMID:30827496	PCS		6/25			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001537	PMID:30827496	PCS		1/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000601	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000722	PMID:30827496	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001539	PMID:30827496	PCS		1/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0004209	PMID:30827496	PCS		4/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000322	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000006	PMID:30424743	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000369	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000126	PMID:30827496	PCS		6/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001655	PMID:30827496	PCS		3/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001792	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000582	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000463	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000023	PMID:30827496	PCS		1/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002120	PMID:30827496	PCS		2/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002164	PMID:30827496	PCS		8/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000460	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0010862	PMID:30424743	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000738	PMID:30424743	PCS		1/1			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002719	PMID:30827496	PCS		3/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001629	PMID:30827496	PCS	HP:0003577	5/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0005709	PMID:30827496	PCS		2/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000414	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000219	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002119	PMID:30827496	PCS		3/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0008755	PMID:30827496	PCS		3/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002558	PMID:30827496	PCS		4/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000776	PMID:30827496	PCS		1/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001320	PMID:30827496	PCS		6/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000154	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000076	PMID:30827496	PCS		3/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000750	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0007925	PMID:30827496	PCS		3/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002650	PMID:30827496	PCS		3/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000431	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0031936	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0001680	PMID:30827496	PCS		2/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002092	PMID:30827496	PCS		2/24			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0005280	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000709	PMID:30424743	PCS	HP:0003621	1/1			P	HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000426	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000107	PMID:30827496	PCS		4/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000505	PMID:30827496	PCS		4/24			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000028	PMID:30827496	PCS		1/6			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-31]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000347	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0002126	OMIM:618454	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618454	Developmental delay with or without dysmorphic facies and autism		HP:0000588	PMID:30827496	PCS		1/24			P	HPO:probinson[2022-10-31]
OMIM:617767	Joubert syndrome 33		HP:0002188	PMID:26167768	PCS		2/6			P	HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0001263	PMID:26167768	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0001252	PMID:26167768	PCS		1/6			P	HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0001251	PMID:26167768	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0000657	PMID:26167768	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0002419	PMID:26167768	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0000007	PMID:26167768	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0000548	PMID:26167768	PCS		0/6			P	HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0001159	PMID:26167768	PCS		1/6			P	HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0000256	PMID:26167768	PCS		1/6			P	HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0002104	PMID:26167768	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-12]
OMIM:617767	Joubert syndrome 33		HP:0001744	PMID:26167768	PCS		0/6			P	HPO:probinson[2023-03-12]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0002257	PMID:23022101	PCS		9/9			P	HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0003621	PMID:23022101	PCS		2/9			C	HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0001696	PMID:23022101;PMID:23849777	PCS		0/10			P	HPO:probinson[2022-02-28];HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0002110	PMID:23022101	PCS		9/9			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0003593	PMID:23022101	PCS		2/9			C	HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0100582	PMID:23022101	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0033542	PMID:23022101	PCS		1/1			P	HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0012207	PMID:23022101	PCS		1/1	MALE		P	HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0011108	PMID:23022101	PCS		9/9			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0200073	PMID:23022101	PCS					P	HPO:skoehler[2013-06-04];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0012265	PMID:23022101;PMID:23849777	PCS		12/12			P	HPO:probinson[2022-02-28];HPO:probinson[2022-02-28];HPO:probinson[2022-02-28];HPO:probinson[2013-04-07];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0011463	PMID:23022101	PCS		2/9			C	HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0000007	PMID:23022101	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0000403	PMID:23022101;PMID:23849777	PCS		11/11			P	HPO:skoehler[2012-11-20];HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0002878	PMID:23849777	PCS		1/1			P	HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0006532	PMID:23022101	PCS					P	HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0002205	PMID:23022101	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0002643	PMID:23022101	PCS		8/9			P	HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0003623	PMID:23022101	PCS		3/9			C	HPO:probinson[2022-02-28];HPO:probinson[2022-02-28]
OMIM:608647	Ciliary dyskinesia, primary, 5		HP:0004469	PMID:23022101	PCS		9/9			P	HPO:probinson[2022-02-28]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000286	PMID:29460469	PCS		5/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000321	PMID:29460469	IEA		10/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000486	PMID:29460469	PCS		26/48			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0010803	PMID:29460469	PCS		8/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000365	PMID:29460469	PCS		13/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0002144	PMID:29460469	PCS		1/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001250	PMID:29460469	PCS		5/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001371	PMID:29460469	PCS		4/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0003196	PMID:29460469	PCS		12/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0002020	PMID:29460469	PCS		3/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0012745	PMID:29460469	PCS		15/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000518	PMID:29460469	PCS		2/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0010055	PMID:29460469	PCS		3/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0011220	PMID:29460469	PCS		13/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001845	PMID:29460469	PCS		5/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001249	PMID:29460469	PCS		19/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000494	PMID:29460469	PCS		3/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000175	PMID:29460469	PCS		2/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001385	PMID:29460469	PCS		3/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000574	PMID:29460469	PCS		5/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000293	PMID:29460469	PCS		7/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001382	PMID:29460469	PCS		4/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0011968	PMID:29460469	PCS		18/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000490	PMID:29460469	PCS		1/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000729	PMID:29460469	PCS		13/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001537	PMID:29460469	PCS		2/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000527	PMID:29460469	PCS		6/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0004209	PMID:29460469	PCS		6/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0001852	PMID:29460469	PCS		9/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0002788	PMID:29460469	PCS		10/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000322	PMID:29460469	PCS		4/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000006	PMID:29460469	PCS					I	HPO:probinson[2020-07-21];HPO:probinson[2022-12-03]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000446	PMID:29460469	PCS		5/21			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000369	PMID:29460469	PCS		12/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0006349	PMID:29460469	PCS		3/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000582	PMID:29460469	PCS		14/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000343	PMID:29460469	PCS		12/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000387	PMID:29460469	PCS		6/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000463	PMID:29460469	PCS		11/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0002002	PMID:29460469	PCS		6/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000540	PMID:29460469	PCS		8/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000023	PMID:29460469	PCS		3/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0002000	PMID:29460469	PCS		14/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000581	PMID:29460469	PCS		10/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0010621	PMID:29460469	PCS		7/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0012368	PMID:29460469	PCS		9/24			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0008070	PMID:29460469	PCS		4/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0011238	PMID:29460469	PCS		9/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000618	PMID:29460469	PCS		2/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0012450	PMID:29460469	PCS		8/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000219	PMID:29460469	PCS		11/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000218	PMID:29460469	PCS		9/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000411	PMID:29460469	PCS		13/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000457	PMID:29460469	PCS		11/24			P	HPO:probinson[2020-07-21];HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000396	PMID:29460469	PCS		9/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0002650	PMID:29460469	PCS		6/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000430	PMID:29460469	PCS		3/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0031936	PMID:29460469	PCS					P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0005280	PMID:29460469	PCS		13/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0400005	PMID:29460469	PCS		6/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000506	PMID:29460469	PCS		13/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000508	PMID:29460469	PCS		8/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000347	PMID:29460469	PCS		14/24			P	HPO:probinson[2020-07-21]
OMIM:618332	Menke-Hennekam syndrome 1		HP:0000028	PMID:29460469	PCS		6/13	MALE		P	HPO:probinson[2020-07-21]
OMIM:615616	Arrhythmogenic right ventricular dysplasia, familial, 13		HP:0003621	PMID:23136403	PCS		2/2			C	HPO:probinson[2022-07-10]
OMIM:615616	Arrhythmogenic right ventricular dysplasia, familial, 13		HP:0011705	PMID:23136403	PCS		1/5			P	HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:615616	Arrhythmogenic right ventricular dysplasia, familial, 13		HP:0005133	PMID:23136403	PCS		2/5			P	HPO:probinson[2022-07-10];HPO:probinson[2022-07-10]
OMIM:615616	Arrhythmogenic right ventricular dysplasia, familial, 13		HP:0011713	PMID:23136403	PCS		2/5			P	HPO:probinson[2022-07-10]
OMIM:615616	Arrhythmogenic right ventricular dysplasia, familial, 13		HP:0004756	PMID:23136403	PCS		2/5			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-07-10]
OMIM:615616	Arrhythmogenic right ventricular dysplasia, familial, 13		HP:0000006	PMID:23136403	PCS					I	HPO:skoehler[2014-02-06];HPO:probinson[2022-07-10]
OMIM:614508	Mirror movements 2		HP:0011463	PMID:22305526	PCS					C	HPO:probinson[2023-05-19]
OMIM:614508	Mirror movements 2		HP:0003829	PMID:22305526	PCS					I	HPO:skoehler[2012-11-18];HPO:probinson[2023-05-19]
OMIM:614508	Mirror movements 2		HP:0003593	PMID:22305526	PCS					C	HPO:probinson[2023-05-19]
OMIM:614508	Mirror movements 2		HP:0001335	PMID:22305526	PCS		10/18			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-05-19]
OMIM:614508	Mirror movements 2		HP:0000006	PMID:22305526	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-19]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0004322	PMID:24762113	PCS		8/9			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0001156	PMID:24762113	PCS		6/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0003088	PMID:24762113	PCS		1/8			P	HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0011800	PMID:24762113	PCS		6/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0005280	PMID:24762113	PCS		3/9			P	HPO:skoehler[2019-04-18]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0010886	PMID:24762113	PCS		1/8			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0100777	OMIM:165800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0010055	OMIM:165800	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0002938	OMIM:165800	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0002515	OMIM:165800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0002007	OMIM:165800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0005616	PMID:24762113	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0009778	PMID:24762113	PCS		3/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0008843	OMIM:165800	IEA					P	HPO:skoehler[2019-04-18]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0000006	PMID:20137779	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-21]
OMIM:165800	Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans		HP:0000303	PMID:24762113	PCS		3/9			P	HPO:probinson[2023-04-21]
OMIM:613267	Corneal dystrophy, fuchs endothelial, 3		HP:0007957	OMIM:613267	TAS				HP:0003676	P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:613267	Corneal dystrophy, fuchs endothelial, 3		HP:0012040	OMIM:613267	TAS					P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:613267	Corneal dystrophy, fuchs endothelial, 3		HP:0003581	OMIM:613267	TAS					C	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:613267	Corneal dystrophy, fuchs endothelial, 3		HP:0000505	OMIM:613267	TAS					P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:613267	Corneal dystrophy, fuchs endothelial, 3		HP:0012038	OMIM:613267	TAS					P	HPO:probinson[2023-02-27];HPO:probinson[2023-02-27]
OMIM:613267	Corneal dystrophy, fuchs endothelial, 3		HP:0000006	PMID:25722209	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-27]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0001234	OMIM:112450	TAS					P	HPO:skoehler[2012-11-16]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0010109	OMIM:112450	TAS					P	HPO:skoehler[2009-02-17]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0009882	OMIM:112450	IEA					P	HPO:iea[2009-02-17]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0010049	OMIM:112450	IEA					P	HPO:iea[2009-02-17]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0009778	OMIM:112450	TAS					P	HPO:skoehler[2009-02-17]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0008080	OMIM:112450	IEA					P	HPO:skoehler[2015-12-30]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0000006	OMIM:112450	IEA					I	HPO:iea[2009-02-17]
OMIM:112450	Brachydactyly, preaxial, with hallux varus and thumb abduction		HP:0010743	OMIM:112450	IEA					P	HPO:iea[2009-02-17]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0010627	OMIM:221750	IEA					P	HPO:skoehler[2010-06-18]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0004322	OMIM:221750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0000407	OMIM:221750	TAS					P	HPO:skoehler[2013-03-14]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0000839	OMIM:221750	TAS					P	HPO:skoehler[2015-01-21]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0000470	OMIM:221750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0008213	OMIM:221750	IEA					P	HPO:iea[2009-02-17]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0000007	OMIM:221750	IEA					I	HPO:iea[2009-02-17]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0000824	OMIM:221750	IEA					P	HPO:iea[2009-02-17]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0001249	OMIM:221750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:221750	Deafness, sensorineural, with pituitary dwarfism		HP:0000830	OMIM:221750	IEA					P	HPO:iea[2009-02-17]
OMIM:273770	THREONINEMIA		HP:0003354	OMIM:273770	IEA					P	HPO:iea[2009-02-17]
OMIM:273770	THREONINEMIA		HP:0001250	OMIM:273770	IEA					P	HPO:iea[2009-02-17]
OMIM:273770	THREONINEMIA		HP:0003296	OMIM:273770	IEA					P	HPO:iea[2009-02-17]
OMIM:273770	THREONINEMIA		HP:0000007	OMIM:273770	IEA					I	HPO:iea[2009-02-17]
OMIM:273770	THREONINEMIA		HP:0001510	OMIM:273770	IEA					P	HPO:iea[2009-02-17]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0000473	PMID:24319291	PCS		1/7			P	HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0003621	PMID:24319291	PCS		1/7			C	HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0003676	PMID:24319291	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0002059	PMID:24319291	PCS		1/7			P	HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0003487	PMID:24319291	PCS		1/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0001310	PMID:24319291	PCS		7/7			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0002497	PMID:24319291	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0001272	PMID:24319291	PCS		1/7			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0003693	OMIM:611302	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0001260	PMID:24319291	PCS		5/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0002066	PMID:24319291	PCS		7/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0002380	OMIM:611302	IEA					P	HPO:skoehler[2010-06-19]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0011448	PMID:24319291	PCS		1/6			P	HPO:probinson[2023-04-08];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0011463	PMID:24319291	PCS		6/7			C	HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0000007	PMID:24319291	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0007663	PMID:24319291	PCS		1/7			P	HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0002359	PMID:24319291	PCS		1/7			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0001257	PMID:24319291	PCS		4/7			P	HPO:skoehler[2010-06-20]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0001268	PMID:24319291	PCS		0/7			P	HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0002599	PMID:24319291	PCS		5/6			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0000666	PMID:24319291	PCS		5/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0001337	PMID:24319291	PCS		5/6			P	HPO:skoehler[2014-02-25];HPO:probinson[2023-04-08]
OMIM:611302	Spastic ataxia 2, autosomal recessive		HP:0001347	PMID:24319291	PCS		6/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-08]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0003577	PMID:25772934	PCS		1/2			C	HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0000486	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001695	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001250	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001274	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0000680	PMID:25772934	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001252	PMID:25772934	PCS		1/2		HP:0012828	P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0005152	PMID:25772934	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0011781	PMID:25772934	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001508	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0000639	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001423	PMID:25772934	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0004756	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001644	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0008936	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0006956	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001663	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0001263	PMID:25772934	PCS		1/2			P	HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0034197	PMID:25772934	PCS		1/2			C	HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0007572	PMID:25772934	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0007398	PMID:25772934	PCS		2/2			P	HPO:probinson[2023-02-05];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0000568	PMID:25772934	PCS		0/2			P	HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0000647	PMID:25772934	PCS		0/2			P	HPO:probinson[2023-02-05];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0000564	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:300952	Linear skin defects with multiple congenital anomalies 3		HP:0000545	PMID:25772934	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-05]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0005990	OMIM:225250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0008191	PMID:16418214	PCS		1/4			P	HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0100028	PMID:16418214	PCS		3/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0033078	PMID:16418214	PCS		4/4			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0032210	PMID:16418214	PCS		1/4			P	HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0002925	PMID:16418214	PCS		4/4			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0000821	PMID:16418214	PCS		4/4			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0000851	OMIM:225250	IEA					P	HPO:skoehler[2015-01-19]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0001510	OMIM:225250	IEA					P	HPO:skoehler[2010-06-20]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0001653	PMID:16418214	PCS		1/4			P	HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0000006	PMID:16418214	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:225250	Hypothyroidism, congenital, nongoitrous, 5		HP:0001655	PMID:16418214	PCS		1/4			P	HPO:probinson[2023-02-12]
OMIM:618440	Oculoskeletodental syndrome		HP:0000286	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0000365	PMID:31034465	PCS		3/5			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0002243	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0004322	PMID:31034465	PCS		5/5			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0005257	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0002162	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0002240	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0000280	PMID:31034465	PCS		3/3			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0010761	PMID:31034465	PCS		3/6			P	HPO:probinson[2019-05-22];HPO:probinson[2019-05-22];HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0003072	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0100864	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0000519	PMID:31034465	PCS	HP:0003577	5/5			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0008155	PMID:31034465	PCS		3/3			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0000158	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0000677	PMID:31034465	PCS		2/3			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0001744	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0002650	PMID:31034465	PCS		5/5			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0000431	PMID:31034465	PCS		2/3			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0002750	PMID:31034465	PCS		2/3			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0001263	PMID:31034465	PCS		2/2			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0000294	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0002150	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0032325	PMID:31034465	PCS		1/3			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0001518	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0000007	PMID:31034465	PCS					I	HPO:probinson[2019-05-22];HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0000821	PMID:31034465	PCS		2/3			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0000766	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0002901	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0002942	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0002987	OMIM:618440	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618440	Oculoskeletodental syndrome		HP:0000501	PMID:31034465	PCS		4/5			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0000028	PMID:31034465	PCS	HP:0003577	1/2			P	HPO:probinson[2019-05-22]
OMIM:618440	Oculoskeletodental syndrome		HP:0000104	OMIM:618440	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001212	PMID:27612186	PCS		2/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0003199	OMIM:617773	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001252	PMID:27612186	PCS	HP:0003577	3/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0003593	OMIM:617773	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0012469	PMID:27612186	PCS		2/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000718	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000316	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0100807	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0003701	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000752	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000358	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001249	PMID:27612186	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0002553	OMIM:617773	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000574	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0002353	OMIM:617773	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0002079	OMIM:617773	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0003487	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001382	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001263	PMID:27612186	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001182	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000448	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000007	PMID:27612186	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000527	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001257	PMID:27612186	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000369	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0002521	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0002169	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0003577	PMID:27612186	PCS		3/3			C	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001310	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001270	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0012444	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000414	PMID:27612186	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0002317	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000218	PMID:27612186	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001347	PMID:27612186	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000698	PMID:27612186	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0008936	PMID:27612186;OMIM:617773	PCS		11/13			P	HPO:probinson[2022-06-16];HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001762	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0002650	PMID:27612186	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000750	OMIM:617773	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0001761	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000276	PMID:27612186	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0031936	PMID:27612186	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0010819	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0005484	OMIM:617773	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0100874	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0032792	PMID:27612186	PCS		2/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000664	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000268	PMID:27612186	PCS		1/3			P	HPO:probinson[2022-06-16]
OMIM:617773	Intellectual developmental disorder, autosomal recessive 61		HP:0000303	PMID:27612186	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-16]
OMIM:619986	Immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection		HP:0025452	PMID:35587511	PCS					P	HPO:probinson[2022-09-05]
OMIM:619986	Immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection		HP:0003621	PMID:35587511	PCS					C	HPO:probinson[2022-09-05]
OMIM:619986	Immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection		HP:0031292	PMID:35587511	PCS					P	HPO:probinson[2022-09-05]
OMIM:619986	Immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection		HP:0011132	PMID:35587511	PCS					P	HPO:probinson[2022-09-05]
OMIM:619986	Immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection		HP:0003829	PMID:35587511	PCS					I	HPO:probinson[2022-09-05]
OMIM:619986	Immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection		HP:0000006	PMID:35587511	PCS					I	HPO:probinson[2022-09-05]
OMIM:619986	Immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection		HP:0002721	PMID:35587511	PCS					P	HPO:probinson[2022-09-05]
OMIM:608653	Deafness, autosomal recessive 32, with or without immotile sperm		HP:0003577	PMID:27259055	PCS		7/7			C	HPO:probinson[2022-02-27]
OMIM:608653	Deafness, autosomal recessive 32, with or without immotile sperm		HP:0000407	PMID:27259055	PCS	HP:0003577	7/7			P	HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:608653	Deafness, autosomal recessive 32, with or without immotile sperm		HP:0000407	PMID:27259055	PCS	HP:0003621				P	HPO:probinson[2022-02-27]
OMIM:608653	Deafness, autosomal recessive 32, with or without immotile sperm		HP:0003251	PMID:27259055	PCS		5/8	MALE		P	HPO:probinson[2022-02-27];HPO:probinson[2022-02-27]
OMIM:608653	Deafness, autosomal recessive 32, with or without immotile sperm		HP:0000007	PMID:27259055	PCS					I	HPO:skoehler[2015-09-11];HPO:probinson[2022-02-27]
OMIM:608653	Deafness, autosomal recessive 32, with or without immotile sperm		HP:0012208	PMID:27259055	PCS					P	HPO:probinson[2022-02-27]
OMIM:608653	Deafness, autosomal recessive 32, with or without immotile sperm		HP:0012864	PMID:27259055	PCS		4/4	MALE		P	HPO:skoehler[2019-02-22];HPO:probinson[2022-02-27]
DECIPHER:18	1p36 microdeletion syndrome		HP:0001250	DECIPHER:18	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:18	1p36 microdeletion syndrome		HP:0000490	DECIPHER:18	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:18	1p36 microdeletion syndrome		HP:0000270	DECIPHER:18	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:18	1p36 microdeletion syndrome		HP:0001252	DECIPHER:18	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:18	1p36 microdeletion syndrome		HP:0000307	DECIPHER:18	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:18	1p36 microdeletion syndrome		HP:0001249	DECIPHER:18	IEA					P	HPO:skoehler[2013-05-29]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000275	OMIM:602418	TAS					P	HPO:probinson[2012-05-01]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000175	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0003027	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000276	OMIM:602418	TAS					P	HPO:probinson[2012-05-01]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0009380	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0005070	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0006495	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000601	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0009623	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0009777	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000218	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000006	OMIM:602418	IEA					I	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000204	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000347	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0002984	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0006315	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:602418	Weyers ulnar ray/oligodactyly syndrome		HP:0000126	OMIM:602418	IEA					P	HPO:iea[2009-02-17]
OMIM:612794	Atrial septal defect 5		HP:0001684	PMID:17947298	PCS	HP:0003577	20/20			P	HPO:probinson[2023-04-03]
OMIM:612794	Atrial septal defect 5		HP:0000006	PMID:17947298	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-03]
OMIM:300615	Brunner syndrome		HP:0100710	OMIM:300615	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300615	Brunner syndrome		HP:0002014	OMIM:300615	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:300615	Brunner syndrome		HP:0001419	PMID:24169519	PCS					I	HPO:skoehler[2015-12-30]
OMIM:300615	Brunner syndrome		HP:0031284	OMIM:300615	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:300615	Brunner syndrome		HP:0000718	PMID:24169519	PCS					P	HPO:probinson[2017-05-29]
OMIM:300615	Brunner syndrome		HP:0000717	PMID:24169519	PCS					P	HPO:skoehler[2014-07-11]
OMIM:300615	Brunner syndrome		HP:0030186	OMIM:300615	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300615	Brunner syndrome		HP:0000744	PMID:24169519	PCS					P	HPO:probinson[2017-05-29]
OMIM:300615	Brunner syndrome		HP:0001270	PMID:24169519	TAS		HP:0040283			P	HPO:skoehler[2014-07-11]
OMIM:300615	Brunner syndrome		HP:0100716	PMID:24169519	PCS					P	HPO:probinson[2017-05-29]
OMIM:300615	Brunner syndrome		HP:0002315	OMIM:300615	IEA					P	HPO:skoehler[2018-10-08]
OMIM:300615	Brunner syndrome		HP:0001249	PMID:24169519	PCS					P	HPO:probinson[2017-05-29]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002861	PMID:35931051	PCS		1/11			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0000164	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0003577	PMID:35931051	PCS		2/9			C	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0001596	PMID:35931051	PCS		9/9			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0004322	PMID:35931051	PCS		2/10			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002020	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0003593	PMID:35931051	PCS		6/9			C	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0010984	PMID:35931051	PCS					I	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0001508	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002719	PMID:35931051	PCS		3/10			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0001903	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0000653	PMID:35931051	PCS		9/9			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0008734	PMID:35931051	PCS		1/11			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0001488	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0004315	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002850	PMID:35931051	PCS		2/9			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0009926	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002015	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0000252	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0003621	PMID:35931051	PCS		1/9			C	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0001000	PMID:35931051	PCS		10/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0006739	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002671	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0031413	PMID:35931051	PCS		2/3			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0008404	PMID:35931051	PCS		10/10			P	HPO:probinson[2022-10-02];HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0001511	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002745	PMID:35931051	PCS		4/10			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0002720	PMID:35931051	PCS		4/9			P	HPO:probinson[2022-10-02]
OMIM:620040	Dyskeratosis congenita, digenic		HP:0001018	PMID:35931051	PCS		1/10			P	HPO:probinson[2022-10-02]
OMIM:620726	Bethlem myopathy 1C		HP:0034392	PMID:17886299	PCS		1/2			P	HPO:probinson[2024-06-24]
OMIM:620726	Bethlem myopathy 1C		HP:0002808	PMID:17886299	PCS		1/2			P	HPO:probinson[2024-06-24]
OMIM:620726	Bethlem myopathy 1C		HP:0001270	PMID:17886299	PCS		1/2			P	HPO:probinson[2024-06-24]
OMIM:620726	Bethlem myopathy 1C		HP:0001324	PMID:17886299	PCS		2/2			P	HPO:probinson[2024-06-24];HPO:probinson[2024-06-24]
OMIM:620726	Bethlem myopathy 1C		HP:0003701	PMID:17886299	PCS		1/2			P	HPO:probinson[2024-06-24]
OMIM:620726	Bethlem myopathy 1C		HP:0000006	PMID:9536084	PCS					I	HPO:probinson[2024-06-24];HPO:probinson[2024-06-24]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0004443	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0004322	PMID:25683121	PCS		6/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0030674	PMID:25683121	PCS		1/1			C	HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0004440	PMID:25683121	PCS		6/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000262	OMIM:616294	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0001252	PMID:25683121	PCS		4/5			P	HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0010862	PMID:25683121	PCS		2/5			P	HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000938	PMID:25683121	PCS		7/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000316	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000238	PMID:25683121	PCS		5/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0008897	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0002757	PMID:25683121	PCS	HP:0030674	1/1			P	HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000218	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0001620	PMID:25683121	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000256	PMID:25683121	PCS		4/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0001562	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000494	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000592	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0001263	PMID:25683121	PCS		0/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0011800	PMID:25683121	PCS		3/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0010537	PMID:25683121	PCS		4/4			P	HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0002808	OMIM:616294	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000308	PMID:25683121	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000926	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000767	PMID:25683121	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000007	PMID:25683121	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000703	OMIM:616294	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0002868	PMID:25683121	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0002007	PMID:25683121	PCS		6/6			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0002645	PMID:25683121	PCS		3/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000520	PMID:25683121	PCS		6/7			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-12]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000883	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616294	Cole-Carpenter syndrome 2		HP:0000325	OMIM:616294	TAS					P	HPO:skoehler[2015-05-31]
OMIM:615945	Spinocerebellar ataxia 37		HP:0002015	OMIM:615945	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615945	Spinocerebellar ataxia 37		HP:0003621	PMID:28686858	PCS		14/30			C	HPO:probinson[2023-04-15];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0003596	PMID:28686858	PCS		4/30			C	HPO:probinson[2023-04-15];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0001272	OMIM:615945	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615945	Spinocerebellar ataxia 37		HP:0001260	PMID:28686858	PCS		27/30			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0001251	PMID:28686858	PCS		27/27			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0000639	OMIM:615945	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615945	Spinocerebellar ataxia 37		HP:0011463	PMID:28686858	PCS		2/30			C	HPO:probinson[2023-04-15];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0011462	PMID:28686858	PCS		10/30			C	HPO:probinson[2023-04-15];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0002317	PMID:28686858	PCS		9/30			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0002359	OMIM:615945	TAS					P	HPO:skoehler[2014-10-06]
OMIM:615945	Spinocerebellar ataxia 37		HP:0001337	OMIM:615945	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615945	Spinocerebellar ataxia 37		HP:0000006	PMID:28686858	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-04-15]
OMIM:615945	Spinocerebellar ataxia 37		HP:0003677	OMIM:615945	TAS					C	HPO:skoehler[2015-12-30]
OMIM:614483	Brain small vessel disease 2		HP:0002069	PMID:30315939	PCS		1/2			P	HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0002301	PMID:22209246	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0002510	PMID:30315939	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0002132	PMID:22209246	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0001263	PMID:30315939	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0002170	PMID:22209246	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0010636	PMID:30315939	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0032391	PMID:30315939	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0003829	PMID:22209246	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0002119	PMID:22209246	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0000565	PMID:30315939	PCS		1/2			P	HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0007359	PMID:30315939	PCS		1/2			P	HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0001510	PMID:30315939	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0000006	PMID:22209246	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-20]
OMIM:614483	Brain small vessel disease 2		HP:0002126	PMID:30315939	PCS		2/2			P	HPO:probinson[2021-02-20]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0004325	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0003510	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0003577	PMID:24389050	PCS		2/2			C	HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000463	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0001156	PMID:24389050	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0002384	OMIM:615789	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0005590	PMID:24389050	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0045075	PMID:24389050	PCS		2/2			P	HPO:probinson[2022-05-08];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000639	OMIM:615789	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0002719	PMID:24389050	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0001903	PMID:24389050	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000938	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0009882	OMIM:615789;PMID:24389050	PCS		12/12			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0009623	OMIM:615789	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0001522	PMID:24389050	PCS		1/2			C	HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000577	OMIM:615789	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000252	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0001762	PMID:24389050	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0002079	PMID:24389050	PCS		1/2			P	HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0005585	OMIM:615789	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0011927	PMID:24389050	TAS					P	HPO:probinson[2015-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0012736	OMIM:615789	TAS					P	HPO:skoehler[2015-08-16]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0011003	OMIM:615789	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0005280	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000308	OMIM:615789	IEA					P	HPO:skoehler[2019-02-22]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0001518	PMID:24389050	TAS		4/4			P	HPO:probinson[2015-05-08];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000506	PMID:24389050	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0002209	PMID:24389050	PCS		2/2			P	HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000007	PMID:24389050	TAS					I	HPO:probinson[2015-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000348	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0002007	PMID:24389050	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0001159	OMIM:615789	IEA					P	HPO:skoehler[2019-09-07]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0004823	PMID:24389050	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-05-08]
OMIM:615789	Short stature with microcephaly and distinctive facies		HP:0000520	PMID:24389050	TAS		2/2			P	HPO:probinson[2015-05-08];HPO:probinson[2022-05-08]
OMIM:614497	Microphthalmia, isolated, with coloboma 7		HP:0003577	PMID:22226084	PCS		8/8			C	HPO:probinson[2023-04-07]
OMIM:614497	Microphthalmia, isolated, with coloboma 7		HP:0000568	OMIM:614497	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614497	Microphthalmia, isolated, with coloboma 7		HP:0000612	PMID:22226084	PCS		8/8			P	HPO:probinson[2023-04-07]
OMIM:614497	Microphthalmia, isolated, with coloboma 7		HP:0000006	PMID:22226084	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-07]
OMIM:614497	Microphthalmia, isolated, with coloboma 7		HP:0031613	PMID:22226084	PCS		8/8			P	HPO:probinson[2023-04-07]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002521	PMID:35880319;PMID:30564627	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002540	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002365	PMID:35880319;PMID:30564627	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002046	PMID:30564627	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0003593	PMID:35880319;PMID:30564627	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0032794	PMID:35880319;PMID:30564627	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001270	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0031960	PMID:35880319;PMID:30564627	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002280	PMID:35880319;PMID:30564627	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0031943	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0012110	PMID:35880319;PMID:30564627	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002719	PMID:35880319;PMID:30564627	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001508	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0000737	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002119	PMID:35880319;PMID:30564627	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0000411	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001348	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0008936	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0003202	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002179	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0030303	PMID:35880319;PMID:30564627	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0000252	PMID:35880319;PMID:30564627	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001344	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002079	PMID:35880319;PMID:30564627	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002310	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001761	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0011968	PMID:35880319;PMID:30564627	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002197	PMID:30564627	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001263	PMID:35880319;PMID:30564627	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0031354	PMID:30564627	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0011097	PMID:35880319;PMID:30564627	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0034295	PMID:35880319;PMID:30564627	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0032792	PMID:35880319;PMID:30564627	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0002509	PMID:30564627	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0000601	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0000007	PMID:30564627	PCS					I	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0000763	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001257	PMID:35880319	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0000347	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:620732	Neurodevelopmental disorder with hyperkinetic movements, seizures and structural brain abnormalities		HP:0001336	PMID:35880319;PMID:30564627	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000286	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0003577	OMIM:245349	TAS					C	HPO:skoehler[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000243	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001332	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001250	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001251	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0003828	OMIM:245349	IEA					M	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000316	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0002317	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0002416	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000218	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001249	OMIM:245349	IEA					P	HPO:skoehler[2010-06-18]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001942	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0003128	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0003348	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000252	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0002510	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000496	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0003542	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001263	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0002928	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0007010	OMIM:245349	TAS					P	HPO:probinson[2012-06-10]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000767	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000007	OMIM:245349	IEA					I	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001338	OMIM:245349	TAS					P	HPO:probinson[2012-06-10]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0000648	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001319	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0007015	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:245349	Pyruvate dehydrogenase e3-binding protein deficiency		HP:0001258	OMIM:245349	IEA					P	HPO:iea[2009-02-17]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0003477	PMID:24354524	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0030237	PMID:24354524	PCS		1/2			P	HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0003596	PMID:24354524	PCS		1/2			C	HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0003376	PMID:24354524	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0001288	PMID:24354524	PCS		3/3			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0003693	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0003584	PMID:24354524	PCS		1/2			C	HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0001284	OMIM:616280	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0002460	PMID:24354524	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0009130	PMID:24354524	PCS		2/2			P	HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0009027	OMIM:616280	TAS					P	HPO:skoehler[2015-04-05]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0002936	PMID:24354524	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0000006	PMID:24354524	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-04]
OMIM:616280	Charcot-Marie-Tooth disease, axonal, type 2U		HP:0003677	PMID:24354524	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-09-04]
OMIM:610829	Holoprosencephaly 9		HP:0006988	PMID:14581620	PCS		1/11			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000286	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0004322	OMIM:610829	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:610829	Holoprosencephaly 9		HP:0001250	OMIM:610829	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610829	Holoprosencephaly 9		HP:0003196	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0001092	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0033725	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0010650	PMID:17096318	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0011220	PMID:17096318	PCS		2/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0003829	PMID:17096318	PCS					I	HPO:iea[2010-03-17]
OMIM:610829	Holoprosencephaly 9		HP:0000238	PMID:14581620	PCS		1/11			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0010290	PMID:14581620	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0003745	PMID:17096318	PCS					I	HPO:iea[2010-03-17]
OMIM:610829	Holoprosencephaly 9		HP:0002536	PMID:17096318	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000358	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0006315	PMID:14581620	PCS		1/11			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000175	PMID:14581620	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000252	PMID:14581620	PCS		2/11			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000054	OMIM:610829	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610829	Holoprosencephaly 9		HP:0000453	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0001263	PMID:14581620	PCS					P	HPO:skoehler[2014-06-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0011800	PMID:14581620	PCS		2/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0100336	PMID:17096318;PMID:14581620	PCS		3/15			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0100337	PMID:17096318;PMID:14581620	PCS		3/15			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000609	PMID:14581620	PCS		1/11			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000528	PMID:17096318	PCS		1/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000327	PMID:17096318;PMID:14581620	PCS		20/20			P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000689	PMID:17096318	PCS		11/14			P	HPO:probinson[2024-03-08];HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000601	PMID:17096318;PMID:14581620	PCS		16/25			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-08];HPO:probinson[2024-03-08];HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000568	OMIM:610829	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610829	Holoprosencephaly 9		HP:0001338	PMID:17096318;PMID:14581620	PCS		12/14			P	HPO:probinson[2024-03-08];HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000400	PMID:17096318	PCS		11/14			P	HPO:probinson[2024-03-08];HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000322	PMID:17096318	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0009932	PMID:14581620	PCS		2/11			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000006	PMID:17096318	PCS					I	HPO:iea[2010-03-17]
OMIM:610829	Holoprosencephaly 9		HP:0000204	PMID:14581620	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000324	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0003577	PMID:17096318	PCS		4/4			C	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000384	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0010627	PMID:14581620	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0010626	PMID:14581620	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000260	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0002714	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000455	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0002436	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000179	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000395	OMIM:610829	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610829	Holoprosencephaly 9		HP:0000871	PMID:14581620	PCS		3/11			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0001360	OMIM:610829	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610829	Holoprosencephaly 9		HP:0001162	PMID:14581620	PCS		2/11			P	HPO:iea[2012-04-24];HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0000272	PMID:17096318;PMID:14581620	PCS		11/14			P	HPO:probinson[2024-03-08];HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000470	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0005280	PMID:17096318	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0100960	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0011272	OMIM:610829	TAS					P	HPO:skoehler[2014-06-24]
OMIM:610829	Holoprosencephaly 9		HP:0000508	PMID:17096318	PCS		1/4			P	HPO:probinson[2024-03-08]
OMIM:610829	Holoprosencephaly 9		HP:0006485	PMID:14581620	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000824	PMID:14581620	PCS					P	HPO:iea[2012-04-24]
OMIM:610829	Holoprosencephaly 9		HP:0000028	OMIM:610829	TAS					P	HPO:skoehler[2014-06-24]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0000486	PMID:28051072	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0002540	PMID:28051072	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0001332	PMID:27164704	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0001250	PMID:27164704	PCS		0/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0002120	PMID:28051072	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0001252	PMID:27164704;PMID:28051072	PCS		4/4			P	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0003593	PMID:28051072	PCS		2/2			C	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0000817	PMID:28051072	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0000954	PMID:28051072	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0000733	PMID:28051072	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0025336	PMID:28051072	PCS		2/2			P	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0002353	PMID:27164704	PCS		2/2			P	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0001344	PMID:27164704	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0002079	PMID:28051072	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0001263	PMID:27164704;PMID:28051072	PCS		4/4			P	HPO:probinson[2022-06-18];HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0011800	PMID:28051072	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0012760	PMID:28051072	PCS		1/2			P	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0000729	PMID:27164704	PCS		2/2			P	HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0000007	PMID:27164704	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0100716	PMID:27164704	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0200134	PMID:28051072	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0002007	PMID:28051072	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0001257	PMID:27164704	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617820	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive		HP:0004305	PMID:28051072	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:159900	Dystonia 11, myoclonic		HP:0000473	PMID:11528394	PCS		37/37			P	HPO:iea[2009-02-17]
OMIM:159900	Dystonia 11, myoclonic		HP:0003621	PMID:11528394	PCS		23/37			C	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:159900	Dystonia 11, myoclonic		HP:0002356	PMID:11528394	PCS		21/37			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:159900	Dystonia 11, myoclonic		HP:0025269	PMID:11528394	PCS		4/37			P	HPO:probinson[2023-02-12]
OMIM:159900	Dystonia 11, myoclonic		HP:0001252	OMIM:159900	TAS		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:159900	Dystonia 11, myoclonic		HP:0030955	PMID:11528394	PCS		1/37			P	HPO:probinson[2023-02-12]
OMIM:159900	Dystonia 11, myoclonic		HP:0000716	OMIM:159900	IEA					P	HPO:iea[2009-02-17]
OMIM:159900	Dystonia 11, myoclonic		HP:0011463	PMID:11528394	PCS		14/37			C	HPO:probinson[2023-02-12]
OMIM:159900	Dystonia 11, myoclonic		HP:0000739	PMID:11528394	PCS		1/37			P	HPO:iea[2009-02-17]
OMIM:159900	Dystonia 11, myoclonic		HP:0003829	PMID:11528394	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-12]
OMIM:159900	Dystonia 11, myoclonic		HP:0000756	OMIM:159900	IEA					P	HPO:iea[2009-02-17]
OMIM:159900	Dystonia 11, myoclonic		HP:0000722	PMID:11528394	PCS		1/37			P	HPO:iea[2009-02-17]
OMIM:159900	Dystonia 11, myoclonic		HP:0000006	PMID:11528394	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:159900	Dystonia 11, myoclonic		HP:0001337	OMIM:159900	IEA					P	HPO:iea[2009-02-17]
OMIM:159900	Dystonia 11, myoclonic		HP:0001336	PMID:11528394	PCS		37/37			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-02-12]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0002751	OMIM:600384	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0001991	OMIM:600384	TAS					P	HPO:skoehler[2013-05-31]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0000252	OMIM:600384	IEA					P	HPO:iea[2009-02-17]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0100543	OMIM:600384	TAS					P	HPO:skoehler[2014-04-04]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0004322	OMIM:600384	PCS					P	HPO:probinson[2012-03-18]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0001449	OMIM:600384	PCS					P	HPO:probinson[2012-03-18]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0010554	OMIM:600384	TAS					P	HPO:skoehler[2012-10-17]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0001159	OMIM:600384	IEA					P	HPO:iea[2009-02-17]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0000006	OMIM:600384	IEA					I	HPO:iea[2009-02-17]
OMIM:600384	Aphalangia, partial, with syndactyly and duplication of metatarsaliv		HP:0001249	OMIM:600384	PCS					P	HPO:probinson[2012-03-18]
OMIM:612780	SESAME syndrome		HP:0004322	OMIM:612780	PCS		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0001272	PMID:19289823	PCS		2/5			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0012606	PMID:19289823	PCS		5/5			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0001250	PMID:19289823	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0001252	PMID:19289823	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0001251	PMID:19289823	PCS		5/5			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0003593	PMID:19289823	PCS		4/4			C	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0001290	OMIM:612780	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612780	SESAME syndrome		HP:0002080	PMID:19289823	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0007182	OMIM:612780	PCS		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0000859	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0002917	PMID:19289823	PCS		5/5			P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0032067	PMID:19289823	PCS		5/5			P	HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0007267	PMID:19289823	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0030083	OMIM:612780	TAS					P	HPO:skoehler[2014-09-21]
OMIM:612780	SESAME syndrome		HP:0003127	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0001249	PMID:19289823	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0000750	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0001960	PMID:19289823	PCS		5/5			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0001263	PMID:19289823	PCS		5/5			P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0002075	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0000848	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0001959	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0000407	PMID:19289823	PCS		5/5			P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0000805	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0000822	PMID:19289823	PCS		0/5			P	HPO:skoehler[2013-05-30];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0000007	PMID:19289823	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0000128	PMID:19289823	PCS		10/10			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05];HPO:probinson[2023-03-05]
OMIM:612780	SESAME syndrome		HP:0002900	PMID:19289823	PCS		5/5			P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0000103	OMIM:612780	PCS					P	HPO:probinson[2012-04-11]
OMIM:612780	SESAME syndrome		HP:0000127	PMID:19289823	PCS		5/5			P	HPO:probinson[2012-04-11];HPO:probinson[2023-03-05]
OMIM:603855	Cystic fibrosis, modifier of, 1		HP:0004401	OMIM:603855	IEA					P	HPO:skoehler[2013-01-09]
OMIM:617808	Coffin-siris syndrome 6		HP:0000286	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0002003	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0004322	PMID:26238514	PCS		4/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0002002	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0001156	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0001250	PMID:26238514	PCS		0/4			P	HP:probinson[2018-05-19];HPO:probinson[2023-02-11]
OMIM:617808	Coffin-siris syndrome 6		HP:0002020	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0003593	PMID:26238514	PCS		4/4			C	HPO:probinson[2023-02-11]
OMIM:617808	Coffin-siris syndrome 6		HP:0001290	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0000280	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0001270	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0100033	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000739	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0100702	PMID:26238514	PCS		1/2			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0006970	PMID:26238514	PCS		1/2			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000733	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0030084	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0000455	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0002019	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000278	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0001249	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0000358	PMID:26238514	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:617808	Coffin-siris syndrome 6		HP:0002751	PMID:26238514	PCS		1/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000175	PMID:26238514	PCS		1/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000494	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000750	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0001263	PMID:26238514	PCS		4/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0045025	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0012758	PMID:26238514	PCS		4/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0005280	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0009110	PMID:26238514	PCS		1/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0001999	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000767	PMID:26238514	PCS		1/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0002705	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000348	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0000405	PMID:26238514	PCS		1/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0002007	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0001357	PMID:26238514	PCS		2/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0002645	PMID:26238514	PCS		2/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0001631	PMID:26238514	PCS		1/4			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0007018	PMID:26238514	PCS					P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000322	OMIM:617808	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617808	Coffin-siris syndrome 6		HP:0000006	PMID:26238514	PCS		1/2			I	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000347	PMID:26238514	PCS		1/2			P	HP:probinson[2018-05-19]
OMIM:617808	Coffin-siris syndrome 6		HP:0000369	PMID:26238514	PCS		4/4			P	HPO:probinson[2023-02-11]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0003596	PMID:32855533	PCS		5/12			C	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0002650	PMID:32855533	PCS		1/8			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0004970	PMID:32855533	PCS		3/11			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0003584	PMID:32855533	PCS		4/12			C	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0001519	PMID:32855533	PCS		2/8			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0011462	PMID:32855533	PCS		3/12			C	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0002616	PMID:32855533	PCS		5/11			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0001647	PMID:32855533	PCS		1/11			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0000767	PMID:32855533	PCS		1/8			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0000316	PMID:32855533	PCS		1/8			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0002108	PMID:32855533	PCS		1/8			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0001659	PMID:32855533	PCS		1/11			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0000218	PMID:32855533	PCS		1/8			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0006510	PMID:32855533	PCS		1/8			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0004933	PMID:32855533	PCS		3/11			P	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0000006	PMID:32855533	PCS					I	HPO:probinson[2022-06-20]
OMIM:619825	Aortic aneurysm, familial thoracic 12		HP:0001369	PMID:32855533	PCS		2/8			P	HPO:probinson[2022-06-20]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003158	PMID:36606057;PMID:17245395;PMID:37487849	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003774	PMID:23826568;PMID:28509303;PMID:23197950;PMID:32274456;PMID:33574344;PMID:34904096;PMID:32847529;PMID:31068150;PMID:15844001;PMID:14569098;PMID:15673476;PMID:23988501;PMID:37487849;PMID:15575003;PMID:14531790;PMID:22034507;PMID:36606057;PMID:21060763;PMID:29513881;PMID:17245395;PMID:27729211;PMID:29569962;PMID:15983957;PMID:27764983;PMID:20151160;PMID:33616882	PCS		91/182			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003676	PMID:12471200	PCS					C	HPO:skoehler[2013-05-07];HPO:probinson[2022-04-01]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003596	PMID:22034507;PMID:28509303;PMID:32847529;PMID:33574344;PMID:29513881;PMID:17245395;PMID:32274456;PMID:14531790	PCS		30/66			C	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000123	OMIM:162000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000089	PMID:22034507;PMID:23826568;PMID:23197950;PMID:23988501;PMID:17245395;PMID:15575003;PMID:27729211;PMID:15844001;PMID:25786455;PMID:27764983;PMID:20151160;PMID:14531790	PCS		17/33			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0001970	PMID:23988501	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0011935	PMID:37487849;PMID:31068150	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000083	PMID:12471200	PCS		12/12			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0012624	PMID:28509303;PMID:29513881;PMID:27729211;PMID:29569962;PMID:20151160;PMID:33616882	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0012625	PMID:22034507;PMID:36606057;PMID:29513881;PMID:27729211;PMID:15844001;PMID:25786455;PMID:20151160;PMID:27764983	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0012626	PMID:22034507;PMID:28509303;PMID:37487849;PMID:27764983	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0012622	PMID:14569098;PMID:23826568;PMID:15673476;PMID:23197950;PMID:32274456;PMID:23988501;PMID:33574344;PMID:34904096;PMID:15575003;PMID:14531790;PMID:22034507;PMID:21060763;PMID:32847529;PMID:15983957	PCS		33/33			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0012623	PMID:22034507;PMID:14569098;PMID:15673476;PMID:29513881;PMID:23988501;PMID:15983957	PCS		23/29			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0011463	PMID:17245395;PMID:37487849;PMID:31068150;PMID:27764983;PMID:33616882	PCS		5/15			C	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0011462	PMID:23826568;PMID:15673476;PMID:23197950;PMID:33574344;PMID:32274456;PMID:23988501;PMID:34904096;PMID:15575003;PMID:25786455;PMID:14531790;PMID:22034507;PMID:32847529;PMID:17245395;PMID:15844001;PMID:27764983;PMID:20151160	PCS		50/89			C	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0004719	PMID:23826568;PMID:23197950;PMID:29513881;PMID:17245395;PMID:37487849;PMID:31068150;PMID:25786455;PMID:15844001;PMID:20151160	PCS		4/23			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0001942	PMID:37487849	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003621	PMID:12471200;PMID:36606057;PMID:21060763;PMID:32847529;PMID:23988501;PMID:17245395;PMID:29569962;PMID:15844001;PMID:20151160	PCS		20/33			C	ORCID:0000-0002-0736-9199[2024-08-08];HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000076	PMID:17245395	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000794	PMID:37487849	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0005565	PMID:36606057;PMID:23826568;PMID:17245395;PMID:37487849;PMID:20151160	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0032948	PMID:14569098;PMID:36606057;PMID:28509303;PMID:32847529;PMID:33574344;PMID:17245395;PMID:37487849;PMID:15575003;PMID:31068150;PMID:25786455;PMID:27764983;PMID:14531790	PCS		21/24			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003165	PMID:36606057;PMID:37487849	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003584	PMID:22034507	PCS		2/19			C	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000790	PMID:23826568;PMID:32847529;PMID:23197950;PMID:32274456;PMID:29513881;PMID:31068150;PMID:25786455	PCS		5/32			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000096	PMID:36606057;PMID:28509303;PMID:32847529;PMID:17245395;PMID:31068150;PMID:15844001;PMID:25786455;PMID:27764983;PMID:14531790	PCS		10/15			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000093	PMID:23826568;PMID:28509303;PMID:23197950;PMID:32274456;PMID:15575003;PMID:25786455;PMID:22034507;PMID:36606057;PMID:21060763;PMID:32847529;PMID:17245395;PMID:29513881;PMID:31068150;PMID:27729211;PMID:15844001;PMID:20151160;PMID:27764983;PMID:33616882	PCS		33/57			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000092	PMID:12471200;PMID:36606057;PMID:28509303;PMID:32847529;PMID:17245395;PMID:37487849;PMID:31068150;PMID:25786455;PMID:14531790	PCS		24/24			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-04-01];ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0012213	PMID:12471200	PCS		28/32			P	HPO:probinson[2022-04-01]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000822	PMID:28509303;PMID:23197950;PMID:23988501;PMID:37487849;PMID:15575003;PMID:14531790;PMID:22034507;PMID:36606057;PMID:32847529;PMID:17245395;PMID:27729211;PMID:29569962;PMID:15983957;PMID:20151160;PMID:33616882	PCS		42/72			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000107	PMID:14569098;PMID:15673476;PMID:23197950;PMID:33574344;PMID:23988501;PMID:25786455;PMID:14531790;PMID:29513881;PMID:17245395;PMID:31068150;PMID:15983957;PMID:20151160;PMID:33616882	PCS		25/65			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000108	PMID:36606057;PMID:15673476;PMID:37487849	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000103	PMID:22034507	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0000006	PMID:12471200	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003259	PMID:23826568;PMID:28509303;PMID:15673476;PMID:23197950;PMID:33574344;PMID:23988501;PMID:37487849;PMID:34904096;PMID:15575003;PMID:36606057;PMID:21060763;PMID:29513881;PMID:17245395;PMID:29569962;PMID:15844001;PMID:27764983;PMID:20151160	PCS		50/57			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0001997	PMID:14569098;PMID:28509303;PMID:23826568;PMID:15673476;PMID:23197950;PMID:33574344;PMID:37487849;PMID:34904096;PMID:15575003;PMID:14531790;PMID:22034507;PMID:36606057;PMID:21060763;PMID:32847529;PMID:17245395;PMID:29513881;PMID:15844001;PMID:15983957;PMID:27764983;PMID:20151160;PMID:33616882	PCS		36/85			P	ORCID:0000-0002-0736-9199[2024-08-08];HPO:iea[2009-02-17];HPO:probinson[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0003138	PMID:36606057;PMID:23826568;PMID:21060763;PMID:23197950;PMID:34904096;PMID:15844001	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0002149	PMID:12471200;PMID:28509303;PMID:23826568;PMID:15673476;PMID:23197950;PMID:23988501;PMID:33574344;PMID:37487849;PMID:34904096;PMID:15575003;PMID:25786455;PMID:14531790;PMID:36606057;PMID:21060763;PMID:32847529;PMID:29513881;PMID:17245395;PMID:29569962;PMID:15844001;PMID:15983957;PMID:20151160;PMID:27764983;PMID:33616882	PCS		100/130			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-01];ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:162000	Tubulointerstitial kidney disease, autosomal dominant, 1		HP:0004722	PMID:32847529;PMID:17245395;PMID:14531790	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-08-08]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0002553	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000582	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000494	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000431	PMID:24623383	PCS		5/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000574	PMID:24623383	PCS		1/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000331	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000463	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000490	PMID:24623383	PCS		2/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000280	PMID:24623383	PCS		5/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0012368	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0012471	PMID:24623383	PCS		5/5			P	HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0011220	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000316	PMID:24623383	PCS		2/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000414	PMID:24623383	PCS		2/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000007	PMID:24623383	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000664	PMID:24623383	PCS		4/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000311	PMID:24623383	PCS		1/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000278	PMID:24623383	PCS		2/5			P	HPO:probinson[2022-06-15];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0000336	PMID:24623383	PCS		3/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2022-06-15]
OMIM:615979	Intellectual developmental disorder, autosomal recessive 45		HP:0001249	PMID:24623383	PCS		5/5			P	HPO:skoehler[2015-01-19];HPO:probinson[2022-06-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002487	OMIM:618285	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0008936	PMID:30343943	PCS		30/30			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002521	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002510	PMID:30343943	PCS		16/30			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0001344	PMID:30343943	PCS		21/24			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002353	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002540	PMID:30343943	PCS		21/24			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002133	PMID:30343943	PCS		2/30			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0001332	PMID:30343943	PCS		12/30			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002376	PMID:30343943	PCS		9/30			P	HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002120	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0007371	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0000639	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0100704	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002803	PMID:30343943	PCS	HP:0003577	13/30			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0002804	PMID:30343943	PCS	HP:0003577				P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0200134	PMID:30343943	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0000256	OMIM:618285	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0000006	PMID:30343943	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-18]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0001347	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618285	Developmental and epileptic encephalopathy 69		HP:0001336	OMIM:618285	IEA					P	HPO:skoehler[2019-02-15]
OMIM:608096	Epilepsy, familial temporal lobe, 2		HP:0002069	PMID:16972079	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:608096	Epilepsy, familial temporal lobe, 2		HP:0002373	OMIM:608096	IEA					P	HPO:iea[2009-02-17]
OMIM:608096	Epilepsy, familial temporal lobe, 2		HP:0002384	OMIM:608096	IEA					P	HPO:iea[2009-02-17]
OMIM:608096	Epilepsy, familial temporal lobe, 2		HP:0002349	OMIM:608096	IEA					P	HPO:iea[2009-02-17]
OMIM:608096	Epilepsy, familial temporal lobe, 2		HP:0032656	PMID:16972079	PCS		4/7			P	HPO:probinson[2021-06-26]
OMIM:608096	Epilepsy, familial temporal lobe, 2		HP:0000006	PMID:16972079	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-26]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0001382	PMID:19557868	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2024-03-08]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0001252	PMID:19557868	PCS		1/10			P	HPO:probinson[2024-03-08];HPO:probinson[2024-03-08]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0001373	PMID:19557868	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-08]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0001065	OMIM:130020	IEA					P	HPO:skoehler[2010-06-20]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0100699	PMID:19557868	PCS		0/10			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-08]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0003738	PMID:19557868	PCS		4/10			P	HPO:probinson[2024-03-08]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0002505	PMID:19557868	PCS		0/10			P	HPO:probinson[2024-03-08]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0002758	OMIM:130020	IEA					P	HPO:iea[2009-02-17]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0000977	OMIM:130020	IEA					P	HPO:iea[2009-02-17]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0001324	PMID:19557868	PCS		2/10			P	HPO:probinson[2024-03-08]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0000006	OMIM:130020	IEA					I	HPO:iea[2009-02-17]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0000974	OMIM:130020	IEA					P	HPO:iea[2009-02-17]
OMIM:130020	Ehlers-danlos syndrome, Hypermobility type		HP:0001634	OMIM:130020	IEA					P	HPO:iea[2009-02-17]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001374	OMIM:618291	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0003577	OMIM:618291	IEA					C	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0031846	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002120	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001371	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0003298	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0006829	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001270	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0012650	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0009487	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0000954	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002878	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0100309	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002119	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0000377	OMIM:618291	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0000256	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001320	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001188	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0003202	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0006956	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001561	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002650	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001762	PMID:27751653	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002871	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001321	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002079	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0011968	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0011800	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001181	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0012510	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0010557	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0034197	PMID:27751653	PCS		1/2			C	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002808	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0034198	PMID:27751653	PCS		1/2			C	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002827	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002828	PMID:27751653	PCS		2/2			P	HPO:probinson[2023-02-23];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002804	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0001558	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0002747	OMIM:618291	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0000960	PMID:27751653	PCS		1/2			P	HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0000006	PMID:27751653	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-23]
OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant		HP:0000347	PMID:27751653	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-23]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000286	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002465	OMIM:251300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0007759	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000486	PMID:26123727	PCS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0004322	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001332	PMID:26123727	PCS		8/15			P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001250	PMID:26123727	PCS		7/15			P	HPO:skoehler[2015-02-22]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000083	OMIM:251300	IEA					P	HPO:skoehler[2018-10-08]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001010	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001252	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001251	OMIM:251300	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0003593	OMIM:251300	IEA					C	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0003073	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000518	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000639	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000316	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001967	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001249	PMID:26123727	PCS		15/15			P	HPO:skoehler[2015-02-22]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0005469	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001188	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002036	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002510	OMIM:251300	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000252	PMID:26123727	PCS		13/15			P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002079	OMIM:251300	TAS					P	HPO:skoehler[2015-02-22]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0011968	OMIM:251300	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001263	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000097	PMID:26123727	PCS					P	HPO:probinson[2017-05-29]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0011800	OMIM:251300	TAS					P	HPO:skoehler[2015-10-05]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000093	PMID:26123727	PCS		6/12			P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0012385	OMIM:251300	TAS					P	HPO:skoehler[2013-10-22]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000448	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000568	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000007	PMID:26123727	PCS					I	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000648	PMID:26123727	PCS		13/14			P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0007676	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000400	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001257	PMID:26123727	PCS		9/15			P	HPO:probinson[2017-05-29]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000369	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002269	PMID:26123727	PCS		0/12			P	HPO:probinson[2017-05-29];HPO:probinson[2024-03-09]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000340	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001792	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002365	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000100	PMID:26123727	PCS					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001272	PMID:26123727	PCS		12/12			P	HPO:skoehler[2015-02-22]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000418	OMIM:251300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001305	OMIM:251300	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002119	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000218	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001302	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001347	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001562	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000154	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0008936	PMID:26123727	PCS		11/15			P	HPO:probinson[2017-05-29]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0002059	PMID:26123727	PCS		8/12			P	HPO:skoehler[2015-02-22]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000750	OMIM:251300	PCS		11/12			P	HPO:probinson[2017-05-29]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001762	OMIM:251300	TAS					P	HPO:skoehler[2015-11-15]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001761	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0005484	OMIM:251300	TAS					P	HPO:skoehler[2015-12-30]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0009473	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001518	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000508	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001511	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0000347	OMIM:251300	IEA					P	HPO:iea[2009-02-17]
OMIM:251300	Galloway-Mowat syndrome 1		HP:0001238	OMIM:251300	TAS					P	HPO:skoehler[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0001595	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000582	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000463	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0004322	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000491	OMIM:122430	IEA					P	HPO:skoehler[2010-06-20]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000272	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0011800	OMIM:122430	TAS					P	HPO:skoehler[2013-11-28]
OMIM:122430	Ramos-Arroyo syndrome		HP:0005280	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0011229	OMIM:122430	TAS					P	HPO:skoehler[2013-05-31]
OMIM:122430	Ramos-Arroyo syndrome		HP:0012155	OMIM:122430	IEA					P	HPO:skoehler[2015-01-27]
OMIM:122430	Ramos-Arroyo syndrome		HP:0001508	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000407	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0007980	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000316	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0007663	OMIM:122430	TAS					P	HPO:skoehler[2015-07-26]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000505	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0001643	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0002007	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000006	OMIM:122430	IEA					I	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0000369	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:122430	Ramos-Arroyo syndrome		HP:0001249	OMIM:122430	IEA					P	HPO:iea[2009-02-17]
OMIM:612964	Premature ovarian failure 7		HP:0008209	PMID:19246354	PCS		4/9	FEMALE		P	HPO:probinson[2013-04-07];HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0000013	PMID:19246354	PCS		2/9	FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0000133	PMID:31361404	PCS					P	HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0001470	PMID:19246354	PCS					I	HPO:probinson[2013-04-07]
OMIM:612964	Premature ovarian failure 7		HP:0011969	PMID:19246354	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0000869	PMID:19246354	PCS		1/9	FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0008232	PMID:19246354	PCS		9/9	FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0008665	PMID:19246354	PCS		2/9	FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0002555	PMID:19246354	PCS		2/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-11]
OMIM:612964	Premature ovarian failure 7		HP:0000786	PMID:19246354	PCS		4/9	FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2020-07-11]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0001254	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0025484	PMID:9590296	PCS		1/2			P	HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0003577	PMID:9590296	PCS		1/4			C	HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0002045	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0010307	OMIM:218700	TAS					P	HPO:skoehler[2017-07-13]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0031507	PMID:9590296	PCS		4/5			P	HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0001252	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0005990	PMID:9590296	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0003270	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0008191	PMID:9590296	PCS		1/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0100028	OMIM:218700	IEA					P	HPO:skoehler[2010-06-18]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0000958	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0008872	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0000851	OMIM:218700	IEA					P	HPO:skoehler[2015-01-19]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0000158	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0002019	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0000853	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0003623	PMID:9590296	PCS		2/4			C	HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0003621	PMID:9590296	PCS		1/4			C	HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0001662	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0002750	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0004491	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0002904	OMIM:218700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0001537	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0002925	PMID:9590296	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0000821	PMID:9590296	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0001615	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0001510	OMIM:218700	IEA					P	HPO:iea[2009-02-17]
OMIM:218700	Hypothyroidism, congenital, nongoitrous, 2		HP:0000006	PMID:9590296	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-28]
OMIM:619831	Spermatogenic failure 71		HP:0003251	PMID:32719396;PMID:33713115	PCS		4/4			P	HPO:probinson[2022-06-27]
OMIM:619831	Spermatogenic failure 71		HP:0011462	PMID:32719396;PMID:33713115	PCS		4/4			C	HPO:probinson[2022-06-27]
OMIM:619831	Spermatogenic failure 71		HP:0034299	PMID:32719396	PCS		2/2			P	HPO:probinson[2022-09-05]
OMIM:619831	Spermatogenic failure 71		HP:0000007	PMID:32719396	PCS					I	HPO:probinson[2022-06-27]
OMIM:619831	Spermatogenic failure 71		HP:0011961	PMID:32719396;PMID:33713115	PCS		4/4			P	HPO:probinson[2022-06-27]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0001771	PMID:18852439	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0005997	PMID:18852439	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0003202	PMID:18852439	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0003236	PMID:18852439	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0010628	PMID:18852439	PCS		1/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0003676	PMID:18852439	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0004322	PMID:18852439	PCS		1/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0002460	PMID:18852439	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0011463	PMID:18852439	PCS		2/2			C	HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0032341	PMID:18852439	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0002938	PMID:18852439	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0000007	PMID:18852439	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0002944	PMID:18852439	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0003701	PMID:18852439	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2022-02-01]
OMIM:255600	Myosclerosis, autosomal recessive		HP:0003306	PMID:18852439	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-01]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0006944	PMID:31439721	PCS		1/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0001771	PMID:31439721	PCS		2/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0003676	PMID:31439721	PCS		3/3			C	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0003431	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0001250	PMID:31439721	PCS		0/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0003593	PMID:27485015	PCS		1/1			C	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0001270	PMID:31439721	PCS		3/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0100297	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0040081	PMID:27485015	PCS		0/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0007340	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0011463	PMID:31439721	PCS		3/3			C	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0009027	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0007002	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0007126	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0008954	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0001324	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0002359	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0007149	PMID:31439721	PCS		1/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0001249	PMID:31439721	PCS		0/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0003447	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0002650	PMID:31439721	PCS		1/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0001284	PMID:27485015	PCS		1/1			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0009053	PMID:31439721	PCS		3/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0001257	PMID:31439721	PCS		1/3			P	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0000006	PMID:27485015	PCS					I	HPO:probinson[2022-12-05]
OMIM:620068	Charcot-Marie-Tooth disease, axonal, type 2II		HP:0008944	PMID:31439721	PCS		3/3			P	HPO:probinson[2022-12-05]
OMIM:610140	Heart-hand syndrome, Slovenian type		HP:0001156	PMID:18611980	PCS		6/14			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-26]
OMIM:610140	Heart-hand syndrome, Slovenian type		HP:0003198	PMID:18611980	PCS		1/14			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-26]
OMIM:610140	Heart-hand syndrome, Slovenian type		HP:0030084	OMIM:610140	TAS					P	HPO:skoehler[2014-09-21]
OMIM:610140	Heart-hand syndrome, Slovenian type		HP:0001159	OMIM:610140	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610140	Heart-hand syndrome, Slovenian type		HP:0010239	OMIM:610140	IEA					P	HPO:skoehler[2010-06-20]
OMIM:610140	Heart-hand syndrome, Slovenian type		HP:0000006	PMID:18611980	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-26]
OMIM:610140	Heart-hand syndrome, Slovenian type		HP:0001644	OMIM:610140	IEA					P	HPO:skoehler[2010-06-19]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002144	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000486	PMID:32335897	PCS		4/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002540	PMID:32335897	PCS		3/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0004322	PMID:32335897	PCS		5/6			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001332	PMID:32335897	PCS		2/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0004684	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001250	PMID:32335897	PCS		2/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0010807	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001252	PMID:29938792;PMID:32335897	PCS		6/6			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002020	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000085	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001251	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000639	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000678	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000278	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001249	PMID:32335897	PCS		6/6			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0003048	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002553	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001188	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000494	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000252	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0003244	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001344	PMID:32335897	PCS		2/5			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0010957	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002673	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001382	PMID:32335897	PCS		3/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0011968	PMID:32335897	PCS		4/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001263	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0003042	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002827	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0004209	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000768	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000047	PMID:32335897	PCS		2/5			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000006	PMID:29938792	PCS					I	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000369	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000385	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0003016	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0003577	PMID:29938792	PCS		1/1			C	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000581	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001508	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000418	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000938	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000218	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0004976	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002677	PMID:29938792;PMID:32335897	PCS		2/8			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001320	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001166	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0002650	PMID:29938792;PMID:32335897	PCS		3/8			P	HPO:probinson[2022-12-04];HPO:probinson[2022-12-04];HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0004993	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000276	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0030048	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000272	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0100760	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0100759	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000348	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0001357	PMID:29938792	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000543	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000303	PMID:32335897	PCS		1/7			P	HPO:probinson[2022-12-04]
OMIM:620083	Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects		HP:0000028	PMID:32335897	PCS		2/5			P	HPO:probinson[2022-12-04]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0001320	PMID:25855803	PCS		2/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0001762	PMID:25855803	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0002089	PMID:25855803	PCS		2/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0001321	PMID:25855803	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0010945	PMID:25855803	PCS		2/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0010557	PMID:25855803	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0012650	PMID:25855803	PCS	HP:0011461	3/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0006380	PMID:25855803	PCS		2/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0010292	PMID:25855803	PCS		1/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0012454	PMID:25855803	PCS		1/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0007033	PMID:25855803	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0011461	PMID:25855803	PCS		3/3			C	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0008796	PMID:25855803	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0002804	PMID:25855803	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0000007	PMID:25855803	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0002119	PMID:25855803	PCS		1/3			P	HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0000268	PMID:25855803	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		HP:0000347	PMID:25855803	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-14]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0000252	PMID:31608932	PCS		4/4			P	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0001561	PMID:31608932	PCS		3/3			P	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0000023	PMID:31608932	PCS		1/3			P	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0007363	PMID:31608932	PCS		3/3			P	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0011461	PMID:31608932	PCS		3/3			C	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0000007	PMID:31608932	PCS					I	HPO:probinson[2022-02-03];HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0001989	PMID:31608932	PCS		3/3			P	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0003811	PMID:31608932	PCS		2/2			C	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0002536	PMID:31608932	PCS		4/4			P	HPO:probinson[2022-02-03]
OMIM:619602	Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies		HP:0002126	PMID:31608932	PCS		4/4			P	HPO:probinson[2022-02-03]
OMIM:614326	Feingold syndrome 2		HP:0004322	PMID:21892160	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0001629	PMID:21892160	PCS		1/14			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0011100	PMID:21892160	PCS		4/13			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0004220	PMID:21892160	PCS		11/14			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0005484	PMID:21892160	PCS		10/14			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0009577	PMID:21892160	PCS		11/14			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0004691	PMID:21892160	PCS		11/14			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0008897	PMID:21892160	PCS		4/14			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0009779	PMID:21892160	PCS		11/14			P	HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0009778	PMID:21892160	PCS		5/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0000006	PMID:21892160	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-08]
OMIM:614326	Feingold syndrome 2		HP:0001249	PMID:21892160	PCS		13/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-08]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000483	PMID:26846096	PCS		1/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0003577	PMID:26846096	PCS		2/2			C	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0007737	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000486	PMID:26846096	PCS		1/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001156	PMID:26846096	PCS		2/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000083	PMID:22353939	PCS		1/3			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0003074	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0010442	PMID:22353939	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000518	PMID:26846096	PCS		1/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000858	PMID:26846096	PCS		1/1			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000510	PMID:22353939;PMID:34212515	PCS		4/4			P	HPO:probinson[2021-07-05];HPO:skoehler[2014-11-26];HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0007843	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001249	PMID:22353939;PMID:34212515	PCS		2/4			P	HPO:probinson[2021-07-05];HPO:skoehler[2014-11-26];HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000750	PMID:26846096	PCS		2/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001162	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001263	PMID:26846096	PCS		2/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0002591	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0100259	PMID:26846096	PCS		2/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001959	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000007	PMID:16380913	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0000546	PMID:26846096	PCS		2/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001956	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001159	PMID:26846096	PCS		2/2			P	HPO:probinson[2021-02-06]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001830	PMID:34212515	PCS		1/1			P	HPO:probinson[2021-07-05]
OMIM:615986	Bardet-Biedl syndrome 9		HP:0001513	PMID:26846096;PMID:22353939	PCS		3/5			P	HPO:probinson[2021-02-06];HPO:skoehler[2014-11-26];HPO:probinson[2021-02-06]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0002014	OMIM:264350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0002013	OMIM:264350	TAS					P	HPO:probinson[2009-02-17]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0002153	PMID:8589714	PCS		10/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0008242	OMIM:264350	TAS					P	HPO:probinson[2009-02-17]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0000859	PMID:8589714	PCS		10/10			P	HPO:probinson[2011-02-06];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0001508	OMIM:264350	TAS					P	HPO:probinson[2012-07-22]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0002902	PMID:8589714	PCS		10/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0001944	PMID:8589714	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0000007	PMID:8589714	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0008872	OMIM:264350	TAS					P	HPO:probinson[2009-02-17]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0002615	PMID:8589714	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0002205	OMIM:264350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0000127	OMIM:264350	TAS					P	HPO:probinson[2009-02-17]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0001942	PMID:8589714	PCS		10/10			P	HPO:probinson[2012-07-22];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0000841	PMID:8589714	PCS					P	HPO:skoehler[2013-06-13];HPO:probinson[2022-03-25]
OMIM:264350	Pseudohypoaldosteronism, type I, autosomal recessive		HP:0003623	PMID:8589714	PCS					C	HPO:probinson[2022-03-25]
OMIM:619164	Immunodeficiency 76		HP:0005403	PMID:30822429	PCS		5/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0002583	PMID:30822429	PCS		1/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0003593	PMID:30822429	PCS		3/5			C	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0010976	PMID:30822429	PCS		1/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0100501	PMID:30822429	PCS		2/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0003819	PMID:30822429	PCS		3/5			C	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0011463	PMID:30822429	PCS		2/5			C	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0000007	PMID:30822429	PCS					I	HPO:probinson[2021-05-07];HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0002716	PMID:30822429	PCS		3/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0001888	PMID:30822429	PCS		5/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0012191	PMID:30822429	PCS		1/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0006532	PMID:30822429	PCS		5/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0001510	PMID:30822429	PCS		3/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0001744	PMID:30822429	PCS		3/5			P	HPO:probinson[2021-05-07]
OMIM:619164	Immunodeficiency 76		HP:0002028	PMID:30822429	PCS		2/5			P	HPO:probinson[2021-05-07]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0008936	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0000252	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0001640	PMID:32969598	PCS	HP:0030674	1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0002376	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0002783	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0030674	PMID:32969598	PCS		1/3			C	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0001250	PMID:32969598	PCS		2/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0002151	PMID:32969598	PCS		3/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0001263	PMID:32969598	PCS		3/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0003593	PMID:32969598	PCS		1/3			C	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0011923	PMID:32969598	PCS		3/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0002280	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0011463	PMID:32969598	PCS		1/3			C	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0011682	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0000817	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0002509	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0000007	PMID:32969598	PCS					I	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0006970	PMID:32969598	PCS		2/3			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0008358	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0000543	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0001257	PMID:32969598	PCS		2/3			P	HPO:probinson[2021-02-19]
OMIM:619170	Mitochondrial complex I deficiency, nuclear type 36		HP:0003348	PMID:32969598	PCS		1/3			P	HPO:probinson[2021-02-19]
OMIM:615992	Bardet-Biedl syndrome 15		HP:0000007	PMID:20671153	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-10]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001254	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0008209	OMIM:603896	PCS					P	HPO:probinson[2012-04-11]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001250	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0004485	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001252	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0006808	OMIM:603896	PCS					P	HPO:probinson[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001290	OMIM:603896	TAS					P	HPO:skoehler[2017-07-13]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0008193	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0008233	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000618	OMIM:603896	PCS		HP:0040283			P	HPO:probinson[2012-04-11]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000712	OMIM:603896	PCS					P	HPO:probinson[2012-04-11]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0002317	OMIM:603896	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001945	OMIM:603896	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000256	OMIM:603896	PCS		HP:0040282			P	HPO:probinson[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000751	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0007305	OMIM:603896	PCS					P	HPO:probinson[2012-04-11]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0003621	OMIM:603896	PCS		HP:0040282			C	HPO:probinson[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001288	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0002354	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0002376	OMIM:603896	PCS					P	HPO:probinson[2012-04-11]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0002352	OMIM:603896	TAS				HP:0012828	P	HPO:probinson[2012-07-15]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001260	OMIM:603896	TAS					P	HPO:skoehler[2012-10-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0002171	OMIM:603896	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000869	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000007	OMIM:603896	IEA					I	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000648	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000746	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0001257	OMIM:603896	IEA					P	HPO:iea[2009-02-17]
OMIM:603896	Leukoencephalopathy with vanishing white matter		HP:0000786	OMIM:603896	IEA					P	HPO:skoehler[2018-10-08]
OMIM:124900	Deafness, autosomal dominant 1		HP:0000132	PMID:26912466	PCS		1/8			P	HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0003621	PMID:26912466	PCS		4/7			C	HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0011891	PMID:26912466	PCS		1/8			P	HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0000407	PMID:26912466	PCS		8/8			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0011463	PMID:26912466	PCS		3/7			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0003540	PMID:26912466	PCS		0/3			P	HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0040185	PMID:26912466	PCS		8/8			P	HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0001873	PMID:26912466	PCS		8/8			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-26]
OMIM:124900	Deafness, autosomal dominant 1		HP:0000006	PMID:26912466	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-26]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0012133	PMID:7949083	PCS					P	HPO:skoehler[2013-06-13];HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0001442	PMID:7949083	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0004861	PMID:7949083	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0003584	PMID:7949083	PCS					C	HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0031385	PMID:7949083	PCS					P	HPO:probinson[2021-07-14];HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0010972	PMID:7949083	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0003745	PMID:7949083	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0001466	PMID:7949083	PCS					I	HPO:probinson[2021-07-14]
OMIM:153550	Chromosome 5q deletion syndrome		HP:0002863	OMIM:153550	TAS					P	HPO:skoehler[2010-06-18]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0002476	OMIM:604121	TAS					P	HPO:skoehler[2013-07-17]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0003676	PMID:22328086	PCS					C	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0003596	PMID:22328086	PCS		2/4			C	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0002354	PMID:22328086	PCS		3/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0001272	OMIM:604121	TAS					P	HPO:skoehler[2013-07-17]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0002494	PMID:22328086	PCS		4/4			P	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0003550	PMID:22328086	PCS		2/4			P	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0001251	PMID:22328086	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0001262	PMID:22328086	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0025233	PMID:22328086	PCS		1/4			P	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0000709	PMID:22328086	PCS		3/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0000716	PMID:22328086	PCS		3/4			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0000726	PMID:22328086	PCS		2/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0000407	PMID:22328086	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0011462	PMID:22328086	PCS		2/4			C	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0002519	PMID:22328086	PCS		2/4			P	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0000648	PMID:22328086	PCS		4/4			P	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0002524	PMID:22328086	PCS		4/4			P	HPO:skoehler[2013-11-18];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0030050	PMID:22328086	PCS		4/4			P	HPO:skoehler[2015-01-20];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0000763	PMID:22328086	PCS		4/4			P	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0001257	OMIM:604121	TAS					P	HPO:skoehler[2013-07-17]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0005978	PMID:22328086	PCS		2/4			P	HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0000006	PMID:22328086	PCS					I	HPO:skoehler[2013-07-17];HPO:probinson[2022-12-20]
OMIM:604121	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant		HP:0001347	OMIM:604121	TAS					P	HPO:skoehler[2013-07-17]
OMIM:610154	Deafness, autosomal recessive 44		HP:0000007	OMIM:610154	IEA					I	HPO:iea[2009-02-17]
OMIM:610154	Deafness, autosomal recessive 44		HP:0000399	OMIM:610154	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0001012	OMIM:176920	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0003676	OMIM:176920	TAS					C	HPO:skoehler[2015-12-30]
OMIM:176920	Proteus syndrome, somatic		HP:0003593	OMIM:176920	TAS					C	HPO:skoehler[2015-12-30]
OMIM:176920	Proteus syndrome, somatic		HP:0012721	OMIM:176920	TAS					P	HPO:skoehler[2014-08-03]
OMIM:176920	Proteus syndrome, somatic		HP:0100764	OMIM:176920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176920	Proteus syndrome, somatic		HP:0007483	OMIM:176920	TAS					P	HPO:probinson[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0012032	OMIM:176920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:176920	Proteus syndrome, somatic		HP:0001528	OMIM:176920	TAS					P	HPO:probinson[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0003745	OMIM:176920	IEA					I	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0007403	OMIM:176920	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0000256	OMIM:176920	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0001744	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0002753	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0001028	OMIM:176920	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0010816	OMIM:176920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:176920	Proteus syndrome, somatic		HP:0002751	OMIM:176920	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0000494	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0003764	OMIM:176920	IEA					P	HPO:skoehler[2010-06-20]
OMIM:176920	Proteus syndrome, somatic		HP:0000276	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0001442	PMID:21793738	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-07-24]
OMIM:176920	Proteus syndrome, somatic		HP:0005465	OMIM:176920	TAS					P	HPO:probinson[2012-04-30]
OMIM:176920	Proteus syndrome, somatic		HP:0001140	OMIM:176920	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0000194	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0002176	OMIM:176920	TAS					P	HPO:probinson[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0004472	OMIM:176920	IEA					P	HPO:iea[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0025092	OMIM:176920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:176920	Proteus syndrome, somatic		HP:0004490	OMIM:176920	TAS					P	HPO:probinson[2012-04-30]
OMIM:176920	Proteus syndrome, somatic		HP:0005280	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:6000009	PMID:31371346	PCS		2/2			P	HPO:probinson[2024-01-06]
OMIM:176920	Proteus syndrome, somatic		HP:0000508	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0002625	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0000268	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:176920	Proteus syndrome, somatic		HP:0003416	OMIM:176920	TAS					P	HPO:probinson[2009-02-17]
OMIM:176920	Proteus syndrome, somatic		HP:0000962	OMIM:176920	TAS					P	HPO:skoehler[2014-07-11]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0002069	PMID:34626583	PCS		11/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000341	PMID:34626583	PCS		1/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0001332	PMID:34626583	PCS		15/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0001250	PMID:34626583	PCS		13/18			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0002121	PMID:34626583	PCS		3/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0001252	PMID:34626583	PCS		13/17			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0003593	PMID:34626583	PCS					C	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0032794	PMID:34626583	PCS		7/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0012469	PMID:34626583	PCS		4/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0100704	PMID:34626583	PCS		15/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0006970	PMID:34626583	PCS					P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000218	PMID:34626583	PCS		1/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0001249	PMID:34626583	PCS					P	HPO:probinson[2022-01-29];HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000215	PMID:34626583	PCS		1/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000252	PMID:34626583	PCS		13/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0002510	PMID:34626583	PCS		12/14			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000494	PMID:34626583	PCS		2/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0002650	PMID:34626583	PCS		7/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0002079	PMID:34626583	PCS					P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0001263	PMID:34626583	PCS		18/18			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000294	PMID:34626583	PCS		1/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0005280	PMID:34626583	PCS		1/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0100952	PMID:34626583	PCS					P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000506	PMID:34626583	PCS		1/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0011099	PMID:34626583	PCS		1/14			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000007	PMID:34626583	PCS					I	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0001257	PMID:34626583	PCS		17/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0007359	PMID:34626583	PCS		4/25			P	HPO:probinson[2022-01-29]
OMIM:619616	Neurodevelopmental disorder with hearing loss and spasticity		HP:0000347	PMID:34626583	PCS		1/25			P	HPO:probinson[2022-01-29]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0003236	PMID:28356563	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0000252	OMIM:617613	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0003676	OMIM:617613	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0000486	PMID:28356563	PCS		1/2			P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0002376	OMIM:617613	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0011968	PMID:28356563	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0001250	PMID:28356563	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0001263	PMID:28356563	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0002151	OMIM:617613	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0003593	PMID:28356563	PCS		2/2			C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0000580	OMIM:617613	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0012448	OMIM:617613	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0000007	PMID:28356563	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0002119	PMID:28356563	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0001302	PMID:28356563	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0001510	OMIM:617613	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0002415	PMID:28356563	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0001257	PMID:28356563	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617613	Multiple mitochondrial dysfunctions syndrome 5		HP:0001347	PMID:28356563	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:601071	Deafness, autosomal recessive 9		HP:0008529	OMIM:601071	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601071	Deafness, autosomal recessive 9		HP:0003577	PMID:10192385	PCS					C	HPO:probinson[2021-02-28]
OMIM:601071	Deafness, autosomal recessive 9		HP:0000407	PMID:10192385	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2021-02-28]
OMIM:601071	Deafness, autosomal recessive 9		HP:0000407	PMID:10192385	PCS	HP:0003577	3/3			P	HPO:probinson[2021-02-28]
OMIM:601071	Deafness, autosomal recessive 9		HP:0004463	OMIM:601071	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601071	Deafness, autosomal recessive 9		HP:0000007	PMID:10192385	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2021-02-28]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000121	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0003510	OMIM:156400	TAS	HP:0003593				P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000365	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0003155	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0005871	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0003273	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0003072	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000938	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000316	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0002737	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0002515	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0003109	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000773	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0002756	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0003026	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000692	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0004676	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000453	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000452	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0003021	OMIM:156400	TAS					P	HPO:probinson[2012-07-28]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0002150	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000829	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0006380	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0100759	OMIM:156400	TAS					P	HPO:probinson[2012-07-28]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0006487	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0004209	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000520	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000006	OMIM:156400	TAS					I	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000248	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0000347	OMIM:156400	TAS					P	HPO:probinson[2009-02-17]
OMIM:156400	Metaphyseal chondrodysplasia, Jansen type		HP:0002148	OMIM:156400	IEA					P	HPO:probinson[2009-02-17]
OMIM:121850	Corneal fleck dystrophy		HP:0000613	OMIM:121850	IEA					P	HPO:skoehler[2010-06-20]
OMIM:121850	Corneal fleck dystrophy		HP:0007962	OMIM:121850	IEA					P	HPO:iea[2009-02-17]
OMIM:121850	Corneal fleck dystrophy		HP:0000006	OMIM:121850	IEA					I	HPO:iea[2009-02-17]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0003621	PMID:34214472	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0020072	PMID:34214472	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0032163	PMID:34214472	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0033510	PMID:34214472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0000403	PMID:34214472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0000007	PMID:34214472	PCS					I	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0032301	PMID:34214472	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0032247	PMID:34214472	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0032215	PMID:34214472	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0550004	PMID:34214472	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:620901	Immunodeficiency 123 with HPV-related verrucosis		HP:0200043	PMID:34214472	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-28]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0001298	PMID:22499348	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0003198	PMID:22499348	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0011968	PMID:22277967	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0030674	PMID:22277967	PCS		1/1			C	HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0001252	PMID:22499348	PCS		1/1			P	HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0001263	PMID:22499348	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0011923	PMID:22499348;PMID:22277967	PCS		2/2			P	HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0001508	PMID:22277967	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0000007	PMID:22277967	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0001511	PMID:22277967	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0003798	PMID:22277967	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0001622	PMID:22277967	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-05]
OMIM:618246	Mitochondrial complex I deficiency, nuclear type 25		HP:0003128	PMID:22499348;PMID:22277967	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-05];HPO:probinson[2023-02-05]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0008209	PMID:27486781	TAS		3/5	FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0003621	PMID:27486781	PCS		1/10			C	HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0000869	PMID:27486781	PCS		1/5	FEMALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0003581	PMID:27486781	PCS		9/10			C	HPO:probinson[2021-07-06];HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0007663	PMID:27486781	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0000007	PMID:27486781	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0002206	PMID:27486781	PCS		1/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0000556	PMID:27486781	PCS		6/6		HP:0003676	P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:617175	Retinal dystrophy with or without extraocular anomalies		HP:0000853	PMID:27486781	PCS		3/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-06]
OMIM:613313	Hemochromatosis, type 2B		HP:0003452	OMIM:613313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613313	Hemochromatosis, type 2B		HP:0001395	PMID:12469120	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0001394	PMID:12469120	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0002240	OMIM:613313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613313	Hemochromatosis, type 2B		HP:0003281	PMID:12469120	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0012463	PMID:12469120	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0000869	PMID:12469120	PCS	HP:0011462	2/2			P	HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0001903	OMIM:613313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613313	Hemochromatosis, type 2B		HP:0011462	PMID:12469120	PCS		2/2			C	HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0000007	PMID:12469120	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0000953	PMID:12469120	PCS		2/2			P	HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0001635	OMIM:613313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613313	Hemochromatosis, type 2B		HP:0001638	OMIM:613313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613313	Hemochromatosis, type 2B		HP:0000135	PMID:12469120	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-04]
OMIM:613313	Hemochromatosis, type 2B		HP:0002910	OMIM:613313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613313	Hemochromatosis, type 2B		HP:0001744	OMIM:613313	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613307	Deafness, autosomal recessive 79		HP:0000750	OMIM:613307	IEA	HP:0011463				P	HPO:skoehler[2013-01-10]
OMIM:613307	Deafness, autosomal recessive 79		HP:0000408	OMIM:613307	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613307	Deafness, autosomal recessive 79		HP:0000407	OMIM:613307	IEA	HP:0011463				P	HPO:skoehler[2013-01-09]
OMIM:613307	Deafness, autosomal recessive 79		HP:0000007	OMIM:613307	TAS					I	HPO:skoehler[2015-12-30]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0001045	PMID:22236196	PCS		4/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0005425	PMID:22236196	PCS		12/27			P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0410135	PMID:22236196	PCS		27/27		HP:0025206	P	HPO:probinson[2020-09-26];HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0002099	PMID:19910034	PCS		9/21			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0003493	PMID:22236196	PCS		13/21			P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0003593	PMID:19910034	PCS					C	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0003193	PMID:22236196	PCS		9/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0010783	PMID:19910034	PCS		20/20		HP:0025206	P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0031972	PMID:19910034	PCS		12/20		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0011971	PMID:19910034	PCS		1/5		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0012203	PMID:22236196	PCS		2/21			P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0100665	PMID:19910034	PCS		6/20		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0011463	PMID:19910034	PCS					C	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0012393	PMID:22236196	PCS		15/27			P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0000403	PMID:22236196	PCS		6/21			P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0000989	PMID:19910034	PCS		20/20		HP:0025206	P	HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0000872	PMID:22236196	PCS		2/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-26]
OMIM:614468	Familial cold autoinflammatory syndrome 3		HP:0000006	PMID:19910034	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-26]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0003202	PMID:29429571	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0002059	PMID:29429571	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0002013	PMID:29429571	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0001250	PMID:29429571	PCS		1/2			P	HPO:skoehler[2019-02-15]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0001263	PMID:29429571	PCS		2/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0002151	PMID:29429571	PCS		2/2			P	HPO:skoehler[2019-02-15]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0003593	PMID:29429571	PCS		2/2			C	HPO:skoehler[2019-02-15];HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0001290	PMID:29429571	PCS		2/2			P	HPO:skoehler[2019-04-18]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0002490	PMID:29429571	PCS		4/4			P	HPO:probinson[2023-06-04];HPO:skoehler[2019-02-15]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0011923	PMID:29429571	PCS		1/1			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0010479	PMID:29429571	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0003819	PMID:29429571	PCS		1/2			C	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0001508	PMID:29429571	PCS		1/2			P	HPO:skoehler[2019-04-18]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0001518	PMID:29429571	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0002902	PMID:29429571	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0000007	PMID:29429571	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0002878	PMID:29429571	PCS		1/2			P	HPO:probinson[2023-06-04]
OMIM:618252	Mitochondrial complex I deficiency, nuclear type 32		HP:0001942	PMID:29429571	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-06-04]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0002223	PMID:12740761;OMIM:137940	PCS		14/14			P	HPO:probinson[2022-05-08];HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000561	PMID:12740761;OMIM:137940	PCS		14/14			P	HPO:probinson[2022-05-08];HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000286	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0003577	PMID:12740761;OMIM:137940	PCS		11/15			C	HPO:probinson[2022-05-08];HPO:skoehler[2015-12-30]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0003676	OMIM:137940	TAS					C	HPO:skoehler[2015-12-30]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0001596	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0010648	PMID:12740761	PCS		2/4			P	HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0005598	OMIM:137940	TAS					P	HPO:probinson[2009-02-17]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000083	OMIM:137940	TAS					P	HPO:probinson[2009-02-17]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0003593	PMID:12740761	PCS		3/5			C	HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0001790	PMID:12740761	PCS	HP:0011461	1/5			P	HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0012622	OMIM:137940	TAS					P	HPO:skoehler[2015-12-30]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0012471	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0011461	PMID:12740761	PCS		1/5			C	HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0007621	OMIM:137940	TAS					P	HPO:probinson[2009-02-17]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000653	OMIM:137940	TAS					P	HPO:probinson[2012-03-01]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0001004	PMID:12740761	PCS		5/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0003189	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000431	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000034	PMID:12740761	PCS		2/2			P	HPO:skoehler[2015-06-22];HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000793	OMIM:137940	TAS					P	HPO:probinson[2009-02-17]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000095	OMIM:137940	TAS					P	HPO:probinson[2015-02-15]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0001480	OMIM:137940	IEA					P	HPO:skoehler[2018-10-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0001263	OMIM:137940	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0100540	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000426	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0002209	PMID:12740761	PCS		4/4			P	HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0003758	OMIM:137940	TAS					P	HPO:probinson[2009-02-17]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0006521	OMIM:137940	TAS					P	HPO:skoehler[2015-12-30]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000300	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000006	PMID:12740761	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-05-08]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000303	OMIM:137940	TAS					P	HPO:skoehler[2015-06-22]
OMIM:137940	Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome		HP:0000962	OMIM:137940	TAS					P	HPO:probinson[2024-12-03]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0010648	PMID:28163941;PMID:19875893;PMID:15731757;PMID:20358619;PMID:16283890	PCS		7/13			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2013-10-22];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0003593	PMID:24220024	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0410151	PMID:23608731	PCS					P	HPO:lccarmody[2018-10-25]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0011934	PMID:15731757	PCS		1/6			P	HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0011463	PMID:28679693	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005807	OMIM:610168	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0002616	PMID:28163941;PMID:19875893;PMID:15731757;PMID:20358619;PMID:24220024;PMID:32528524;PMID:18084123;PMID:28679693;PMID:16283890	PCS		19/20			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001647	PMID:15731757	PCS	HP:0003577	2/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001647	PMID:18084123	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001647	PMID:20358619	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001647	PMID:16283890	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001647	PMID:28679693	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000316	PMID:28163941;PMID:19875893;PMID:15731757;PMID:20358619;PMID:24220024;PMID:18084123;PMID:16283890	PCS		16/17			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0004959	PMID:15731757;PMID:28679693;PMID:16283890;PMID:16027248	PCS		5/49			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000238	PMID:19875893;PMID:15731757;PMID:18084123;PMID:16283890	PCS		3/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001643	PMID:15731757	PCS	HP:0003623	5/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001643	PMID:18084123	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001643	PMID:20358619	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001643	PMID:24220024	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001643	PMID:16283890	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001643	PMID:28679693	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0004955	OMIM:610168	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001763	PMID:24344637	PCS					P	HP:probinson[2018-04-29]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000278	PMID:19875893;PMID:15731757;PMID:20358619;PMID:32528524;PMID:18084123;PMID:28679693;PMID:16283890	PCS		10/16			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001249	PMID:15731757	PCS		2/10			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000175	PMID:19875893;PMID:15731757;PMID:32528524;PMID:16283890	PCS		4/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0004970	OMIM:610168	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0004970	PMID:16027248	PCS	HP:0003581	17/40			P	HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001382	PMID:19875893;PMID:15731757;PMID:20358619;PMID:24220024;PMID:18084123;PMID:16283890	PCS		14/16			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001263	PMID:19875893;PMID:15731757;PMID:18084123;PMID:16283890	PCS		2/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001065	PMID:24344637	PCS					P	HP:probinson[2018-04-29]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005182	PMID:15731757	IEA	HP:0003577	1/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005182	PMID:18084123	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005182	PMID:20358619	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005182	PMID:28679693	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0012499	PMID:16027248	PCS	HP:0003581	3/40			P	HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0030745	PMID:15731757	PCS	HP:0011461	3/8			P	HPO:probinson[2021-10-21];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0030745	PMID:18084123	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0030745	PMID:20358619	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0030745	PMID:16283890	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0030745	PMID:28679693	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0012385	PMID:28163941;PMID:19875893;PMID:15731757;PMID:18084123;PMID:16283890	PCS		9/14			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2013-10-22];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0100259	PMID:15731757;PMID:16283890	PCS		1/10			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0100775	PMID:15731757;PMID:24220024;PMID:18084123;PMID:16283890	PCS		3/6			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0002308	PMID:15731757;PMID:18084123;PMID:16283890	PCS		2/9			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000767	PMID:28163941;PMID:19875893;PMID:20358619;PMID:18084123;PMID:24344637	PCS		13/16			P	HP:probinson[2018-04-29];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001537	OMIM:610168	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000766	PMID:15731757	PCS		7/10			P	HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0002108	PMID:24344637	PCS					P	HP:probinson[2018-04-29]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000768	PMID:28163941;PMID:19875893;PMID:20358619;PMID:18084123;PMID:24344637	PCS		11/16			P	HP:probinson[2018-04-29];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000520	PMID:19875893;PMID:15731757;PMID:16283890	PCS		8/11			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000006	PMID:15731757	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001655	PMID:19875893;PMID:28679693	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005116	PMID:28163941;PMID:19875893;PMID:15731757;PMID:24220024;PMID:32528524;PMID:18084123;PMID:28679693;PMID:16283890	PCS		15/15			P	HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0003577	PMID:19875893;PMID:20358619	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001156	OMIM:610168	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000023	PMID:20358619;PMID:24220024	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0003179	PMID:24344637	PCS					P	HP:probinson[2018-04-29]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005113	PMID:16027248	PCS	HP:0003581	1/40			P	HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0005112	PMID:16027248	PCS	HP:0003584	1/40			P	HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000939	PMID:20358619	PCS		1/1			P	HPO:skoehler[2012-11-18];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0031252	PMID:15731757;PMID:20358619;PMID:32528524	PCS		3/10			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0004937	PMID:15731757;PMID:28679693;PMID:16283890;PMID:16027248	PCS		6/51			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000977	PMID:19875893;PMID:15731757;PMID:20358619;PMID:16283890	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0004933	PMID:28163941;PMID:20358619;PMID:32528524;PMID:18084123;PMID:28679693;PMID:16027248	PCS		23/47			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000577	PMID:15731757;PMID:16283890	PCS		6/10			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001166	PMID:28163941;PMID:19875893;PMID:15731757;PMID:20358619;PMID:18084123;PMID:28679693;PMID:16283890	PCS		10/16			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001363	PMID:19875893;PMID:15731757;PMID:32528524;PMID:18084123;PMID:16283890	PCS		3/11			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0003621	PMID:20358619	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0003302	PMID:24344637	PCS					P	HP:probinson[2018-04-29]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0002650	PMID:28163941;PMID:19875893;PMID:15731757;PMID:20358619;PMID:24220024;PMID:18084123;PMID:16283890	PCS		11/16			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001762	PMID:19875893;PMID:15731757;PMID:20358619;PMID:24220024;PMID:18084123;PMID:28679693;PMID:16283890	PCS		6/16			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000193	PMID:28163941;PMID:19875893;PMID:15731757;PMID:20358619;PMID:24220024;PMID:32528524;PMID:18084123;PMID:16283890	PCS		12/15			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000592	PMID:19875893;PMID:15731757;PMID:20358619;PMID:18084123;PMID:16283890	PCS		7/13			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000272	PMID:19875893;PMID:15731757;PMID:32528524;PMID:18084123;PMID:28679693;PMID:16283890	PCS		9/14			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001083	PMID:28163941;PMID:19875893;PMID:15731757;PMID:20358619;PMID:24220024;PMID:32528524;PMID:18084123;PMID:28679693;PMID:24344637;PMID:16283890	PCS		0/44			P	HP:probinson[2018-04-29];HPO:probinson[2024-03-14];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001519	PMID:19875893;PMID:15731757;PMID:20358619;PMID:18084123;PMID:16283890	PCS		4/15			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2024-03-31];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0009473	OMIM:610168	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0012163	PMID:16027248	PCS		2/40			P	HPO:probinson[2021-05-23]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001159	OMIM:610168	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001631	PMID:15731757;PMID:20358619;PMID:18084123;PMID:16283890	PCS		3/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0004944	PMID:15731757;PMID:16283890;PMID:16027248	PCS		5/50			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0000347	OMIM:610168	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610168	Loeys-Dietz syndrome 2		HP:0001634	PMID:28163941;PMID:19875893;PMID:15731757;PMID:28679693;PMID:16283890	PCS		3/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-05-23];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:618534	Immunodeficiency 64		HP:0002783	PMID:27776107	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0003496	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0001890	PMID:29155103	PCS	HP:0011463	2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0003493	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0025289	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0032218	PMID:28822832;PMID:27776107	PCS		2/2			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0033207	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-13]
OMIM:618534	Immunodeficiency 64		HP:0100721	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0001508	PMID:27776107	PCS	HP:0003593	1/1		HP:0012828	P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0002719	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0031394	PMID:27776107	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0012191	PMID:28822832;PMID:27776107	PCS		2/2			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0002716	PMID:28822832	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0001744	PMID:28822832	PCS		1/1			P	HPO:probinson[2020-05-19];HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0004315	PMID:28822832	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0025379	PMID:29155103	PCS		1/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0002110	PMID:27776107	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0032069	PMID:29155103	PCS		1/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0003261	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0031379	PMID:28822832	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0031381	PMID:27776107	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0100759	PMID:27776107	PCS		1/1			P	HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0000007	PMID:27776107	PCS					I	HPO:probinson[2020-05-19];HPO:probinson[2020-05-19]
OMIM:618534	Immunodeficiency 64		HP:0001973	PMID:29155103	PCS	HP:0003593	1/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0001433	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:618534	Immunodeficiency 64		HP:0003237	PMID:29155103	PCS		2/2			P	HPO:probinson[2020-10-02]
OMIM:617607	Amelogenesis imperfecta, type IIIB		HP:0000705	PMID:27412008	IEA		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-20]
OMIM:617607	Amelogenesis imperfecta, type IIIB		HP:0006285	PMID:27412008	PCS		1/1			P	HPO:probinson[2021-02-20];HPO:probinson[2021-02-20]
OMIM:617607	Amelogenesis imperfecta, type IIIB		HP:0003593	PMID:27412008	PCS					C	HPO:probinson[2021-02-20]
OMIM:617607	Amelogenesis imperfecta, type IIIB		HP:0000006	PMID:27412008	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-02-20]
OMIM:611276	Glaucoma 1, open angle, H		HP:0100018	PMID:26162006	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:611276	Glaucoma 1, open angle, H		HP:0001123	PMID:26162006	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:611276	Glaucoma 1, open angle, H		HP:0007906	PMID:26162006	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:611276	Glaucoma 1, open angle, H		HP:0003581	PMID:26162006	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:611276	Glaucoma 1, open angle, H		HP:0012108	PMID:26162006	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:611276	Glaucoma 1, open angle, H		HP:0007663	PMID:35490425	PCS					P	HPO:probinson[2024-07-06]
OMIM:611276	Glaucoma 1, open angle, H		HP:0012796	PMID:35490425	PCS					P	HPO:probinson[2024-07-06]
OMIM:611276	Glaucoma 1, open angle, H		HP:0000006	PMID:26162006	PCS					I	ORCID:0000-0002-0736-9199[2024-07-06]
OMIM:609439	Deafness, autosomal recessive 48		HP:0001751	PMID:18505454	TAS					P	HPO:probinson[2012-07-16]
OMIM:609439	Deafness, autosomal recessive 48		HP:0000007	OMIM:609439	TAS					I	HPO:probinson[2009-02-17]
OMIM:609439	Deafness, autosomal recessive 48		HP:0011476	OMIM:609439	TAS	HP:0003577			HP:0012832	P	HPO:probinson[2012-07-16]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0001332	PMID:23001123	PCS		2/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0002063	OMIM:615010	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0002240	PMID:23001123	PCS		1/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0003593	PMID:23001123	PCS		11/14			C	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0012229	PMID:23001123	PCS		1/11			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0034513	PMID:23001123	PCS		6/7			P	HPO:probinson[2024-01-16]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0000639	PMID:23001123	PCS		1/14			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0000737	PMID:23001123	PCS		7/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0011463	PMID:23001123	PCS		1/14			C	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0002514	PMID:23001123	PCS		14/14			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0002415	PMID:23001123	PCS		11/14			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0001744	PMID:23001123	PCS		1/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0003623	PMID:23001123	PCS		2/14			C	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0000252	PMID:23001123	PCS		5/14			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0002376	PMID:23001123	PCS		3/14			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0011968	PMID:23001123	PCS		6/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0009709	PMID:23001123	PCS		10/10			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0002371	OMIM:615010	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0011344	PMID:23001123	PCS		14/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0001878	PMID:23001123	PCS		3/14			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0000007	PMID:23001123	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0002505	OMIM:615010	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0009710	PMID:23001123	PCS		1/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0001511	PMID:23001123	PCS		1/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0001873	PMID:23001123	PCS		2/14			P	HPO:probinson[2022-12-10]
OMIM:615010	Aicardi-Goutieres syndrome 6		HP:0001337	OMIM:615010	TAS					P	HPO:skoehler[2014-05-04]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0005876	PMID:14508707	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0002014	PMID:14508707	PCS		16/29			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000275	PMID:12973667	PCS		3/5			P	HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0003676	PMID:14508707	PCS					C	HPO:skoehler[2013-01-21];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0001371	PMID:12973667	PCS		4/5			P	HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0001482	PMID:12214284;PMID:12973667	PCS		34/35			P	HPO:probinson[2014-05-24];HPO:probinson[2022-05-02];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0003593	PMID:14508707	PCS		22/30			C	HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000280	PMID:12973667	PCS		4/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0001072	PMID:12973667	PCS		3/5			P	HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000939	PMID:12973667	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0002719	PMID:12973667;PMID:14508707	PCS		17/35			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-05-02];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0001508	PMID:12973667;PMID:14508707	PCS		19/35			P	HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0002829	PMID:12973667	PCS		4/5			P	HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0011463	PMID:14508707	PCS		8/30			C	HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000938	PMID:12973667	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000007	PMID:14508707	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000169	PMID:12973667	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000212	PMID:12973667;PMID:14508707	PCS		33/35			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0002797	PMID:12973667	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0001249	PMID:14508707	PCS		0/30			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-02]
OMIM:228600	Hyaline fibromatosis syndrome		HP:0000369	PMID:12973667	PCS		3/5			P	HPO:probinson[2022-05-02]
OMIM:144010	Hypercholesterolemia, familial, 2		HP:0003124	OMIM:144010	PCS		5/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:144010	Hypercholesterolemia, familial, 2		HP:0001084	OMIM:144010	IEA					P	HPO:iea[2009-02-17]
OMIM:144010	Hypercholesterolemia, familial, 2		HP:0003141	PMID:7883971	PCS		7/8			P	HPO:probinson[2021-06-24]
OMIM:144010	Hypercholesterolemia, familial, 2		HP:0001114	OMIM:144010	IEA					P	HPO:iea[2009-02-17]
OMIM:144010	Hypercholesterolemia, familial, 2		HP:0000006	PMID:7883971	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:144010	Hypercholesterolemia, familial, 2		HP:0001677	PMID:7883971	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-06-24]
OMIM:247990	Macdermot-Winter syndrome		HP:0002553	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0000252	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0002057	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0001250	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0000050	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0100490	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0001263	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0000294	OMIM:247990	TAS					P	HPO:skoehler[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0000007	OMIM:247990	IEA					I	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0002119	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0000400	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0001511	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0001522	OMIM:247990	IEA					C	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0006610	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0000358	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:247990	Macdermot-Winter syndrome		HP:0002236	OMIM:247990	TAS					P	HPO:skoehler[2012-09-18]
OMIM:247990	Macdermot-Winter syndrome		HP:0000126	OMIM:247990	IEA					P	HPO:iea[2009-02-17]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0008935	OMIM:614859	TAS					P	HPO:probinson[2013-02-24]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0003577	PMID:26094004	PCS		1/1			C	HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0000431	OMIM:614859	TAS		1/1			P	HPO:skoehler[2017-07-13]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0000260	PMID:26094004	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0001250	PMID:26094004	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0002033	PMID:26094004	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0001252	PMID:26094004	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0002240	OMIM:614859	TAS					P	HPO:probinson[2013-02-24]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0001284	PMID:26094004	PCS		1/1		HP:0003676	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0001290	OMIM:614859	TAS				HP:0003676	P	HPO:skoehler[2017-07-13]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0033643	PMID:26094004	PCS		1/1			P	HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0012368	PMID:26094004	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0010655	OMIM:614859	TAS					P	HPO:probinson[2013-02-24]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0002617	OMIM:614859	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0000348	PMID:26094004	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0008872	OMIM:614859	TAS					P	HPO:probinson[2013-02-24]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0000007	PMID:9354782	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0000113	PMID:26094004	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:614859	Peroxisome biogenesis disorder 3A (Zellweger)		HP:0000369	PMID:26094004	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-08]
OMIM:306700	Hemophilia A		HP:0003125	PMID:8259143	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:306700	Hemophilia A		HP:0005261	PMID:34017743	PCS		96/151			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-07];HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0040242	PMID:8259143	PCS					P	HPO:probinson[2022-03-07]
OMIM:306700	Hemophilia A		HP:0001419	PMID:8259143	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-07]
OMIM:306700	Hemophilia A		HP:0000979	PMID:34017743	PCS		7/151			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0000978	PMID:34017743	PCS		132/151			P	HPO:probinson[2009-02-17];HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0000967	PMID:34017743	PCS		7/151			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0002758	OMIM:306700	IEA					P	HPO:iea[2009-02-17]
OMIM:306700	Hemophilia A		HP:0001934	PMID:34017743	PCS		116/151			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0002249	PMID:34017743	PCS		19/151			P	HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0000421	PMID:34017743	PCS		21/151			P	HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0003645	PMID:8259143	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-07]
OMIM:306700	Hemophilia A		HP:0002248	PMID:34017743	PCS		19/151			P	HPO:probinson[2024-03-09]
OMIM:306700	Hemophilia A		HP:0000225	PMID:34017743	PCS		39/151			P	HPO:probinson[2024-03-09]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0002014	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0000870	PMID:31263451	PCS					P	HPO:probinson[2019-09-07]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0002893	PMID:11836268;PMID:15292304	PCS		164/354			P	HPO:probinson[2022-03-31];HPO:skoehler[2010-06-18];HPO:probinson[2021-05-08]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0004398	OMIM:131100	IEA					P	HPO:skoehler[2010-06-20]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0002044	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0003581	PMID:11836268	PCS					C	HPO:probinson[2022-03-31]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0001031	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0100570	PMID:15292304	PCS		5/30			P	HPO:skoehler[2013-05-31];HPO:probinson[2021-05-08]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0003072	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0030404	PMID:31263451	TAS					P	HPO:skoehler[2015-06-22];HPO:probinson[2019-09-07]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0100633	OMIM:131100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0008261	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0000957	OMIM:131100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0012197	PMID:15292304	PCS		3/30			P	HPO:skoehler[2013-03-15];HPO:probinson[2021-05-08]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0009720	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0008256	PMID:11836268;PMID:15292304	PCS		58/354			P	HPO:iea[2009-02-17];HPO:probinson[2021-05-08];HPO:probinson[2022-03-31]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0001943	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0000854	OMIM:131100	TAS					P	HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0000845	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0003118	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0000006	OMIM:131100	IEA					I	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0007449	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0002897	OMIM:131100	IEA					P	HPO:iea[2009-02-17]
OMIM:131100	Multiple endocrine neoplasia 1		HP:0006767	PMID:31263451;OMIM:131100	PCS		22/40			P	HPO:probinson[2009-02-17];HPO:skoehler[2017-07-13];HPO:probinson[2019-09-07];HPO:probinson[2021-05-08]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0011859	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0003493	PMID:27965258	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0001890	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0002240	PMID:27965258	PCS		1/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0003593	PMID:27965258	PCS		3/3			C	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0001097	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0032061	PMID:27965258	PCS		1/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0000958	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0001508	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0100646	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0000613	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0000554	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0000972	PMID:27965258	PCS		3/3			P	HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0007502	PMID:27965258	PCS		3/3			P	HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0001744	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0005764	PMID:27965258	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0025092	PMID:27965258	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0003261	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0011227	PMID:27965258	PCS		3/3			P	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0011496	PMID:27965258	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0033001	PMID:27965258	PCS		1/3			P	HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0000007	PMID:27965258	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0001954	PMID:27965258	PCS		3/3			P	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0001510	PMID:27965258	PCS		2/3		HP:0012826	P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0000006	PMID:27965258	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:617388	Autoinflammation with arthritis and dyskeratosis		HP:0003237	PMID:27965258	PCS		1/3			P	HPO:probinson[2020-11-26]
OMIM:609808	Hamartoma, precalcaneal congenital fibrolipomatous		HP:0010566	OMIM:609808	IEA					P	HPO:skoehler[2015-01-27]
OMIM:609808	Hamartoma, precalcaneal congenital fibrolipomatous		HP:0000006	OMIM:609808	IEA					I	HPO:iea[2009-02-17]
OMIM:609808	Hamartoma, precalcaneal congenital fibrolipomatous		HP:0000951	OMIM:609808	IEA					P	HPO:iea[2009-02-17]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000286	PMID:36604604	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0003577	PMID:36604604	PCS		1/3			C	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000486	PMID:34379057;PMID:34764295	PCS		3/6			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0002188	PMID:34379057	PCS		1/2			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001250	PMID:34764295	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0002360	PMID:34379057;PMID:36604604	PCS		5/6			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001252	PMID:36604604	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0002020	PMID:34379057	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0003593	PMID:34379057;PMID:36604604	PCS		5/6			C	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0010863	PMID:36604604	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001270	PMID:34379057;PMID:34764295	PCS		6/6			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0010864	PMID:34379057;PMID:34764295;PMID:36604604	PCS		7/9			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001508	PMID:34379057	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000716	PMID:36604604	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000319	PMID:34379057	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0011463	PMID:34764295	PCS		3/3			C	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000718	PMID:34764295	PCS		2/2			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0005709	PMID:34379057	PCS		2/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000733	PMID:34764295	PCS		1/1			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000736	PMID:34379057	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000219	PMID:34379057	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0008897	PMID:34379057	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000218	PMID:34379057	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000752	PMID:34379057	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001324	PMID:36604604	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0002017	PMID:34379057	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001320	PMID:34379057	PCS		1/2			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0002311	PMID:36604604	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0011808	PMID:36604604	PCS		2/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000750	PMID:34379057;PMID:34764295	PCS		6/6			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001344	PMID:36604604	PCS		3/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0002079	PMID:34379057	PCS		1/2			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0001684	PMID:34379057	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0033838	PMID:36604604	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0005484	PMID:34379057;PMID:34764295;PMID:36604604	PCS		5/9			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0007010	PMID:34379057;PMID:34764295	PCS		6/6			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000729	PMID:34764295	PCS		1/3			P	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0000007	PMID:34379057	PCS					I	HPO:probinson[2023-06-15]
OMIM:620242	Neurodevelopmental disorder with poor growth and behavioral abnormalities		HP:0007018	PMID:34764295;PMID:36604604	PCS		5/5			P	HPO:probinson[2023-06-15]
OMIM:610381	Cone-Rod dystrophy 11		HP:0007924	OMIM:610381	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610381	Cone-Rod dystrophy 11		HP:0000980	OMIM:610381	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610381	Cone-Rod dystrophy 11		HP:0000608	PMID:15028672	PCS					P	HPO:probinson[2013-03-30]
OMIM:610381	Cone-Rod dystrophy 11		HP:0000613	OMIM:610381	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:610381	Cone-Rod dystrophy 11		HP:0000548	PMID:15028672	PCS					P	HPO:probinson[2013-03-30]
OMIM:610381	Cone-Rod dystrophy 11		HP:0007401	OMIM:610381	TAS				HP:0003676	P	HPO:skoehler[2015-08-16]
OMIM:610381	Cone-Rod dystrophy 11		HP:0011504	OMIM:610381	TAS					P	HPO:skoehler[2015-08-16]
OMIM:610381	Cone-Rod dystrophy 11		HP:0000006	PMID:15028672	PCS					I	HPO:probinson[2013-01-09]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0006519	OMIM:178500	IEA					P	HPO:iea[2009-02-17]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0001394	OMIM:178500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0002094	PMID:19100526	PCS					P	HPO:probinson[2020-06-11]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0012735	PMID:19100526	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-06-11]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0002092	OMIM:178500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0031950	PMID:19100526	PCS					P	HPO:probinson[2020-10-28]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0010702	OMIM:178500	IEA					P	HPO:iea[2009-02-17]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0045051	PMID:19100526	PCS					P	HPO:probinson[2020-06-11]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0032977	PMID:3702942	PCS					P	HPO:probinson[2020-06-14]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0100759	PMID:30854216	PCS		50%			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-06-11]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0002206	PMID:19100526	PCS		11/15			P	HPO:probinson[2009-02-17];HPO:probinson[2020-10-28]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0000006	PMID:19100526	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-10-28]
OMIM:178500	Pulmonary fibrosis, idiopathic		HP:0002875	OMIM:178500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:618905	Silver-Russell syndrome 2		HP:0001476	PMID:11829489	PCS	HP:0003593	3/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0004322	PMID:11829489	PCS		4/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0002750	PMID:11829489	PCS		2/3			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0000592	PMID:11829489	PCS		3/4			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0004482	PMID:11829489	PCS		5/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0004691	PMID:11829489	PCS		1/4			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0032384	PMID:11829489	IEA					I	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0011342	PMID:11829489	PCS		3/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0000975	PMID:11829489	PCS		2/4			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0001998	PMID:11829489	PCS	HP:0003623	1/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0004209	PMID:11829489	PCS		5/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0002714	PMID:11829489	PCS		4/5			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0001511	PMID:11829489	PCS	HP:0030674	4/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0002007	PMID:11829489	PCS		4/4			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0001466	PMID:11829489	IEA					I	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0000325	PMID:11829489	PCS		4/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0000347	PMID:11829489	PCS		3/5			P	HPO:probinson[2020-08-12]
OMIM:618905	Silver-Russell syndrome 2		HP:0000963	PMID:11829489	PCS		2/5			P	HPO:probinson[2020-08-12]
OMIM:302200	Cataract, congenital total, with posterior sutural opacities in heterozygotes		HP:0100018	OMIM:302200	TAS	HP:0003577		MALE		P	HPO:probinson[2009-02-17]
OMIM:302200	Cataract, congenital total, with posterior sutural opacities in heterozygotes		HP:0001141	OMIM:302200	TAS			MALE		P	HPO:probinson[2009-02-17]
OMIM:302200	Cataract, congenital total, with posterior sutural opacities in heterozygotes		HP:0001417	PMID:19414485	PCS					I	HPO:probinson[2009-02-17]
OMIM:302200	Cataract, congenital total, with posterior sutural opacities in heterozygotes		HP:0010695	OMIM:302200	TAS			FEMALE		P	HPO:probinson[2013-10-13]
OMIM:613850	Inosine triphosphatase deficiency		HP:6000510	PMID:12384777	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:613850	Inosine triphosphatase deficiency		HP:0000007	PMID:12384777	PCS					I	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:613850	Inosine triphosphatase deficiency		HP:6000511	PMID:12384777	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-08-04]
OMIM:613688	Long QT syndrome 2		HP:0001663	OMIM:613688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613688	Long QT syndrome 2		HP:0025708	PMID:34502138	PCS		1/1			C	HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0001695	PMID:34357002	PCS		1/4			P	HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0011463	PMID:34357002	PCS		1/4			C	HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0003581	PMID:34901807;PMID:34357002	PCS		4/5			C	HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0001657	PMID:34357002	PCS		4/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0005184	PMID:34901807	PCS		1/1			P	HPO:probinson[2022-07-09];HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0034303	PMID:34357002	PCS		3/3			P	HPO:probinson[2022-09-05]
OMIM:613688	Long QT syndrome 2		HP:0001664	OMIM:613688	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613688	Long QT syndrome 2		HP:0001279	PMID:34357002	PCS		3/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0001645	PMID:34502138;PMID:34357002	PCS		2/5			P	HPO:probinson[2022-07-09];HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:613688	Long QT syndrome 2		HP:0000006	PMID:7889573	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-09]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0000286	OMIM:135400	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0000494	OMIM:135400	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0009928	PMID:19463983	PCS		HP:0040283			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-12]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0004540	PMID:19463983	PCS	HP:0003577				P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-12]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0000998	OMIM:135400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0000414	PMID:19463983	PCS		HP:0040283			P	HPO:skoehler[2014-08-24];HPO:probinson[2023-03-12]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0000007	PMID:19463983	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0000169	PMID:19463983	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0001007	OMIM:135400	IEA					P	HPO:iea[2009-02-17]
OMIM:135400	Hypertrichosis terminalis, generalized, with or without gingival hyperplasia		HP:0012810	PMID:19463983	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-12]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001298	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001397	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001399	PMID:11687800	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0002045	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001250	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001271	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001252	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0002240	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0003593	PMID:11687800	PCS					C	HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0003073	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001508	PMID:11687800	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0000639	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001409	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001405	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0006254	PMID:11687800	PCS		19/19			P	HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0008872	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001404	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001943	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0002910	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0000952	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001744	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001347	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0003128	PMID:11687800	PCS		19/19			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0003623	PMID:11687800	PCS					C	HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0002059	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0000252	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001541	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0002013	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0011924	PMID:11687800	PCS					P	HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0011923	PMID:11687800	PCS					P	HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0002909	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0006581	PMID:11687800	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0002904	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0000007	PMID:11687800	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0000549	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0008347	PMID:11687800	PCS					P	HPO:probinson[2022-12-02]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001510	OMIM:251880	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001873	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:251880	Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)		HP:0001413	OMIM:251880	IEA					P	HPO:iea[2009-02-17]
OMIM:206700	Gillespie syndrome		HP:0002421	PMID:27108797	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002540	PMID:27108798	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001256	PMID:27108797;PMID:27108798;PMID:35743164;PMID:28698159	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002342	PMID:27108797;PMID:28698159	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001250	PMID:27108797	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001252	PMID:27108798;PMID:35743164	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001251	PMID:37964426;PMID:27108797;PMID:27108798;PMID:35743164;PMID:28698159	PCS		16/16			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002020	PMID:27108798	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0030011	PMID:27108797	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0003593	PMID:27108797;PMID:27108798;PMID:35743164;PMID:28698159	PCS		5/14			C	ORCID:0000-0002-0736-9199[2024-07-17];HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0001290	PMID:27108797;PMID:28698159	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-07-17];HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0033725	PMID:27108797	PCS		1/4			P	HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0000716	PMID:27108798	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000639	PMID:27108797;PMID:35743164;PMID:28698159	PCS		9/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001328	PMID:27108798	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0025336	PMID:27108797;PMID:27108798;PMID:28698159	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001642	PMID:28698159	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001249	PMID:27108797	PCS		3/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0001660	PMID:27108797	PCS	HP:0003577	1/5			P	HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0025335	PMID:27108797	PCS		5/5			P	HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0100021	PMID:37964426;PMID:27108797;PMID:27108798;PMID:35743164;PMID:28698159	PCS		0/16			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002194	PMID:37964426;PMID:28698159	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002071	PMID:27108797	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0007750	PMID:27108798	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000007	PMID:27108797	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0000526	PMID:37964426;PMID:27108797	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0007676	PMID:27108797;PMID:27108798;PMID:35743164;PMID:28698159	PCS		14/14			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000006	PMID:27108797	PCS					I	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0001336	PMID:27108797	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0004689	PMID:27108797	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0003577	PMID:37964426;PMID:27108797;PMID:27108798	PCS		10/12			C	ORCID:0000-0002-0736-9199[2024-07-17];HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0001272	PMID:37964426;PMID:27108797;PMID:27108798;PMID:35743164	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-07-17];HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0001350	PMID:27108797;PMID:28698159	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001270	PMID:27108797;PMID:35743164	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0100275	PMID:35743164	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000657	PMID:28698159	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0007663	PMID:28698159	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002119	PMID:27108797	PCS		1/4			P	HPO:probinson[2022-06-14]
OMIM:206700	Gillespie syndrome		HP:0006855	PMID:28698159	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002015	PMID:28698159	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000750	PMID:27108798	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002650	PMID:27108798;PMID:28698159	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001321	PMID:37964426;OMIM:206700;PMID:27108798	PCS		17/17			P	ORCID:0000-0002-0736-9199[2024-07-17];HPO:iea[2009-02-17]
OMIM:206700	Gillespie syndrome		HP:0031936	PMID:27108798;PMID:35743164	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001288	PMID:27108797	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0007928	PMID:28698159	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002174	PMID:27108797;PMID:28698159	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001081	PMID:27108798	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000826	PMID:28698159	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002808	PMID:27108797	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0009751	PMID:27108797	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000508	PMID:35743164;PMID:28698159	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001999	PMID:27108797	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0009830	PMID:27108797	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0007256	PMID:27108797;PMID:28698159	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0000505	PMID:27108797;PMID:27108798	PCS		12/12			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-14];ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0001510	PMID:28698159	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:206700	Gillespie syndrome		HP:0002522	PMID:27108797	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-17]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000286	PMID:15150541	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0007759	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0010804	OMIM:612582	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0002023	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000486	PMID:15150541	PCS		3/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001492	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001250	PMID:15150541	PCS		1/6			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000160	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001252	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0010609	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0003593	PMID:15150541	PCS		1/6			C	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001290	OMIM:612582	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0012745	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000316	PMID:15150541	PCS		5/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001328	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001009	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000678	OMIM:612582	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000238	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-01]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001643	PMID:15150541	PCS		2/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0003745	PMID:15150541	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001885	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001249	OMIM:612582	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000358	PMID:15150541	PCS		3/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000494	PMID:15150541	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001385	OMIM:612582	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001382	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001263	PMID:15150541	PCS		5/6			P	HPO:skoehler[2014-04-04];HPO:probinson[2021-07-01]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0011800	OMIM:612582	TAS					P	HPO:skoehler[2013-11-28]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000407	PMID:15150541	PCS		3/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-01]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0009891	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000767	PMID:15150541	PCS		2/6			P	HPO:probinson[2021-07-01]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001537	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0004209	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000248	PMID:15150541	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000204	PMID:15150541	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000369	PMID:15150541	PCS		3/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001655	PMID:15150541	PCS		2/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0003577	PMID:15150541	PCS		5/6			C	HPO:probinson[2021-07-04];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0004467	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000540	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001274	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000580	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001270	PMID:15150541	PCS		4/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-01]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001629	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0012450	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000337	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001305	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000659	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000218	PMID:15150541	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000256	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0007700	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0002236	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000577	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000750	OMIM:612582;PMID:15150541	PCS		12/16			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-01]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000592	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000272	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000470	PMID:15150541	PCS		1/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0005280	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001838	OMIM:612582	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0006482	OMIM:612582	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000627	PMID:15150541	PCS		1/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0000506	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001837	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001636	OMIM:612582	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0002007	OMIM:612582	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612582	Chromosome 6pter-p24 deletion syndrome		HP:0001631	PMID:15150541	PCS		1/6			P	HPO:probinson[2021-07-04]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0002751	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0001762	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0003431	OMIM:607831	TAS					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0003693	OMIM:607831	TAS					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0001284	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0002460	OMIM:607831	TAS					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0003450	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0003593	OMIM:607831	TAS					C	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0001171	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0003380	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0000007	OMIM:607831	IEA					I	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0002936	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0003701	OMIM:607831	IEA					P	HPO:iea[2009-02-17]
OMIM:607831	Charcot-Marie-Tooth disease, axonal, type 2K		HP:0000006	OMIM:607831	IEA					I	HPO:iea[2009-02-17]
OMIM:202200	Glucocorticoid deficiency 1		HP:0000098	OMIM:202200	IEA					P	HPO:iea[2009-02-17]
OMIM:202200	Glucocorticoid deficiency 1		HP:0003577	PMID:8227361	PCS		1/1			C	HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0001250	OMIM:202200	IEA					P	HPO:iea[2009-02-17]
OMIM:202200	Glucocorticoid deficiency 1		HP:0003154	PMID:8227361	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0040084	PMID:8227361	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0040085	PMID:8227361	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0008163	PMID:8227361	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0001508	OMIM:202200	IEA					P	HPO:iea[2009-02-17]
OMIM:202200	Glucocorticoid deficiency 1		HP:0002719	OMIM:202200	IEA					P	HPO:iea[2009-02-17]
OMIM:202200	Glucocorticoid deficiency 1		HP:0031074	PMID:8227361	PCS		1/1			P	HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0007440	PMID:8227361	PCS	HP:0003577	1/1			P	HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0001988	PMID:8227361	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0000007	PMID:8227361	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:202200	Glucocorticoid deficiency 1		HP:0000953	OMIM:202200	IEA					P	HPO:iea[2009-02-17]
OMIM:202200	Glucocorticoid deficiency 1		HP:0005616	OMIM:202200	IEA					P	HPO:iea[2009-02-17]
OMIM:202200	Glucocorticoid deficiency 1		HP:0001259	PMID:8227361	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-24]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0002663	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0004688	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0008905	OMIM:250220	TAS					P	HPO:skoehler[2010-06-20]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003498	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001156	OMIM:250220	TAS					P	HPO:skoehler[2015-04-05]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003375	OMIM:250220	TAS					P	HPO:skoehler[2013-08-18]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001252	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000262	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0010049	OMIM:250220	IEA					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001290	OMIM:250220	TAS					P	HPO:skoehler[2017-07-13]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0011675	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0009381	OMIM:250220	TAS					P	HPO:probinson[2012-06-10]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0010230	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0007187	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0008798	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000878	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0006059	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000774	OMIM:250220	TAS					P	HPO:skoehler[2010-06-20]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000773	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0002657	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000358	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0009803	OMIM:250220	IEA					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003026	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0012819	OMIM:250220	IEA					P	HPO:skoehler[2018-10-08]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001762	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003025	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0002132	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001582	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003021	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000470	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003085	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0031233	PMID:24706940	PCS					P	HPO:probinson[2018-04-13]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0004491	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0005280	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003180	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000926	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0002869	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000007	OMIM:250220	TAS					I	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000887	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0008786	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001631	OMIM:250220	TAS					P	HPO:probinson[2009-02-17]
OMIM:250220	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001831	OMIM:250220	TAS					P	HPO:probinson[2012-06-10]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0002421	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000582	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0002540	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000486	PMID:29878067	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001310	PMID:29878067	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001332	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000540	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001250	PMID:29878067	PCS		2/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0003196	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001251	PMID:29878067	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0003593	PMID:29878067	PCS		2/4			C	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0010841	PMID:29878067	PCS		1/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0010862	PMID:29878067	PCS		4/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0040080	PMID:29878067	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0008070	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000316	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000657	PMID:29878067	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0030084	PMID:29878067	PCS		2/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001007	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001249	PMID:29878067	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001347	PMID:29878067	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0003623	PMID:29878067	PCS		2/4			C	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0006855	PMID:29878067	PCS		1/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0008936	PMID:29878067	PCS		4/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000252	PMID:29878067	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000750	PMID:29878067	PCS		4/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001321	PMID:29878067	PCS		3/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000490	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001263	PMID:29878067	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0045025	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0002194	PMID:29878067	PCS		4/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0012434	PMID:29878067	PCS		4/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0002509	PMID:29878067	PCS		2/4			P	HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001159	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0001257	OMIM:618087	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000006	PMID:29878067	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits		HP:0000303	PMID:29878067	PCS		1/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001252	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001097	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0009064	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0011220	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0007485	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0002616	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0100807	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000238	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000278	PMID:20979188;PMID:21594993	PCS		2/2			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001763	PMID:26860060	PCS					P	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0005328	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000995	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000098	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001187	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000494	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000490	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0011003	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0008081	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0100578	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0100775	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000767	PMID:26860060	PCS					P	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0002705	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0003758	PMID:26860060	PCS					P	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000520	PMID:20979188;PMID:21594993	PCS		2/2			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000325	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000006	PMID:20979188	PCS					I	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0030799	PMID:26860060	PCS					P	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0003691	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000460	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001270	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000418	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0007663	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0008872	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000337	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000978	PMID:26860060	PCS					P	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000218	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000774	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000256	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001622	PMID:21594993	PCS		1/1			P	HPO:probinson[2017-06-23];HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001562	PMID:26860060	PCS					P	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001166	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001363	PMID:26860060	PCS					P	HPO:probinson[2017-06-23]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001083	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0012759	PMID:21594993	PCS		0/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0100960	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0002808	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000426	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0000822	OMIM:616914	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001511	PMID:20979188	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:616914	Marfan lipodystrophy syndrome		HP:0001634	PMID:21594993	PCS		1/1			P	HPO:probinson[2021-05-27]
OMIM:203650	Alopecia-intellectual disability syndrome 1		HP:0002289	PMID:28054173	PCS		3/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:203650	Alopecia-intellectual disability syndrome 1		HP:0001596	PMID:28054173	PCS		7/7			P	HPO:probinson[2023-02-11];HPO:probinson[2023-02-11]
OMIM:203650	Alopecia-intellectual disability syndrome 1		HP:0000007	PMID:28054173	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-11]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000494	PMID:31649276	IEA		6/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000175	PMID:31649276	PCS		3/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000252	PMID:31649276	PCS		1/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000452	PMID:31649276	PCS		2/6			P	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000272	PMID:31649276	PCS		6/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0009554	PMID:31649276	PCS		1/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0008872	PMID:31649276	PCS		5/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000405	PMID:31649276	PCS		5/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000652	PMID:31649276	PCS		3/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000006	PMID:31649276	PCS					I	HPO:probinson[2020-08-31];HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000347	PMID:31649276	PCS		5/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0001249	PMID:31649276	PCS		0/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0000324	PMID:31649276	PCS		2/6			P	HPO:probinson[2020-08-31]
OMIM:618939	Treacher-Collins syndrome 4		HP:0004887	PMID:31649276	PCS	HP:0003623	3/6			P	HPO:probinson[2020-08-31]
OMIM:621160	Diarrhea 14, congenital 		HP:0002014	PMID:40174224	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621160	Diarrhea 14, congenital 		HP:0003577	PMID:40174224	PCS		2/2			C	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621160	Diarrhea 14, congenital 		HP:0033994	PMID:40174224	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:621160	Diarrhea 14, congenital 		HP:0000007	PMID:40174224	PCS					I	ORCID:0000-0002-0736-9199[2025-10-08]
OMIM:609820	Erythrocytosis, familial, 3		HP:0001900	OMIM:609820	IEA					P	HPO:iea[2009-02-17]
OMIM:609820	Erythrocytosis, familial, 3		HP:0001899	OMIM:609820	IEA					P	HPO:iea[2009-02-17]
OMIM:609820	Erythrocytosis, familial, 3		HP:0000006	OMIM:609820	IEA					I	HPO:iea[2009-02-17]
OMIM:609820	Erythrocytosis, familial, 3		HP:0001898	OMIM:609820	IEA					P	HPO:iea[2009-02-17]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001298	PMID:27040692	PCS					P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0007957	PMID:27040691	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0006989	PMID:27040692	PCS					P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000365	PMID:27040691;PMID:27040692;PMID:36522252	PCS		1/24			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000486	PMID:30103036;PMID:27275012;PMID:36522252	PCS		7/11			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002263	PMID:27040692;PMID:37876076;PMID:36273129	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003593	PMID:37876076;PMID:30103036;PMID:27275012;PMID:29283439;PMID:36522252	PCS		7/20			C	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001290	PMID:36522252	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0010841	PMID:29283439;PMID:36522252	PCS		6/11			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0033725	PMID:32363625;PMID:29283439	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000518	PMID:27040692	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000639	PMID:36522252	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0012471	PMID:27040691;PMID:37876076;PMID:36273129	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001845	PMID:27275012	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000238	PMID:36522252	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000878	PMID:27040691;PMID:27040692	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003623	PMID:27275012;PMID:32363625	PCS		4/5			C	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002553	PMID:27040692;PMID:36273129;PMID:36522252	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000252	PMID:27040691;PMID:27040692;PMID:29283439	PCS		1/26			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];HPO:probinson[2024-03-15];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001344	PMID:27040691;PMID:37876076;PMID:30103036;PMID:32363625;PMID:36522252	PCS		18/24			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002155	PMID:36522252	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003124	PMID:36522252	PCS		3/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000490	PMID:27040691;PMID:27040692;PMID:30103036;PMID:36273129	PCS		6/21			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0033454	PMID:27040692;PMID:36522252	PCS		7/10			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0012736	PMID:27040692	PCS		5/5			P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001182	PMID:32363625	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0012697	PMID:27040692	PCS					P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0034392	PMID:32363625	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000767	PMID:36273129	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000007	PMID:27040692	PCS					I	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001338	PMID:29283439	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000527	PMID:27040691;PMID:36273129	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000520	PMID:27275012	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000248	PMID:37876076;PMID:30103036;PMID:27275012	PCS		5/6			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000369	PMID:36522252	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000341	PMID:27040692;PMID:37876076;PMID:30103036;PMID:29283439	PCS		14/16			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];HPO:probinson[2024-03-15];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003577	PMID:36273129;PMID:29283439;PMID:36522252	PCS		12/15			C	ORCID:0000-0002-0736-9199[2024-10-14];HPO:skoehler[2017-07-13];HPO:probinson[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000340	PMID:27040691;PMID:37876076;PMID:36273129	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000582	PMID:27040691;PMID:37876076;PMID:36273129	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000343	PMID:27040691;PMID:30103036;PMID:36273129	PCS		3/16			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000463	PMID:27040692;PMID:37876076;PMID:36273129	PCS		4/7			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0010945	PMID:27040691	PCS	HP:0011461	1/13			P	HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001272	PMID:27275012;PMID:36273129;PMID:32363625	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003693	PMID:29283439	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003690	PMID:32363625;PMID:29283439	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001270	PMID:27040691;PMID:37876076;PMID:30103036;PMID:27275012;PMID:36273129;PMID:32363625;PMID:29283439;PMID:36522252	PCS		34/35			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0012444	PMID:27040692	PCS					P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0100704	PMID:27040692;PMID:27275012;PMID:36522252	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000337	PMID:27040691;PMID:36273129	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0006970	PMID:27040691;PMID:37876076;PMID:36273129	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002119	PMID:27040692;PMID:32363625	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000218	PMID:36522252	PCS		2/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003327	PMID:32363625	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000212	PMID:27040692;PMID:37876076;PMID:36273129	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001320	PMID:27040692	PCS					P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001562	PMID:27040691	PCS	HP:0030674	1/11			P	HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0009826	PMID:29283439	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001561	PMID:36522252	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000750	PMID:27040691;PMID:36273129	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002650	PMID:27040691;PMID:30103036;PMID:32363625	PCS		4/17			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002133	PMID:30103036;PMID:32363625;PMID:29283439	PCS		0/11			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001321	OMIM:616900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002376	PMID:27040691;PMID:27040692;PMID:32363625;PMID:29283439;PMID:36522252	PCS		11/34			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];ORCID:0000-0002-0736-9199[2024-10-14];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000194	PMID:27040691;PMID:30103036;PMID:36273129	PCS		4/16			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0005487	PMID:27040691;PMID:37876076;PMID:36273129;PMID:36522252	PCS		2/21			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001284	PMID:29283439	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000470	PMID:27040691	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002093	PMID:27040692;PMID:30103036;PMID:29283439	PCS		10/15			P	HPO:skoehler[2019-09-07];HPO:probinson[2024-10-14];ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0100288	PMID:30103036	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0008180	PMID:32363625	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0011471	PMID:27040692	PCS		5/5			P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001837	PMID:27040691	PCS		1/13			P	HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000508	PMID:27040692	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0030890	PMID:29283439	PCS		6/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001558	PMID:27040691	PCS	HP:0030674	1/11			P	HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001558	PMID:36522252	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000347	PMID:36522252	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000286	PMID:27040691;PMID:37876076;PMID:36273129	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002465	PMID:27040691	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0010804	PMID:27040691;PMID:37876076;PMID:36273129;PMID:36522252	PCS		7/21			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14];HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001250	PMID:27040691;PMID:27040692;PMID:30103036;PMID:27275012;PMID:36273129;PMID:29283439;PMID:36522252	PCS		26/37			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];ORCID:0000-0002-0736-9199[2024-10-14];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002187	PMID:29283439;PMID:36522252	PCS		14/14			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001252	PMID:27040691;PMID:27040692;PMID:37876076;PMID:30103036;PMID:27275012;PMID:36273129;PMID:32363625;PMID:29283439	PCS		35/35			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0006829	PMID:27040692	PCS		5/5			P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0012708	PMID:27040692	PCS		3/3			P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0010884	PMID:29283439	PCS		8/8			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000280	PMID:27040691;PMID:27040692;PMID:37876076;PMID:36273129;PMID:29283439;PMID:36522252	PCS		17/34			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14];HPO:skoehler[2017-07-13];HPO:probinson[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000316	PMID:37876076;PMID:36273129	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000954	PMID:27275012	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000158	PMID:27040691;PMID:27040692;PMID:37876076;PMID:36273129;PMID:29283439;PMID:36522252	PCS		14/34			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001007	PMID:27040691;PMID:36273129;PMID:32363625;PMID:36522252	PCS		4/22			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003444	PMID:29283439;PMID:36522252	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001265	PMID:27040691;PMID:27040692;PMID:37876076;PMID:36273129;PMID:32363625;PMID:36522252	PCS		20/25			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14];HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002750	PMID:27040691	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002079	PMID:27040691	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0011968	PMID:37876076;PMID:36522252	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001263	PMID:27040691;PMID:27040692;PMID:37876076;PMID:30103036;PMID:27275012;PMID:32363625;PMID:36522252	PCS		32/32			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0033383	PMID:29283439;PMID:36522252	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0012020	PMID:27040692	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000565	PMID:27040692	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0003557	PMID:32363625	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002283	PMID:27040691;PMID:36273129;PMID:32363625;PMID:29283439	PCS		8/21			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000262	PMID:36522252	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002280	PMID:32363625	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000939	PMID:27040692;PMID:29283439	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000414	PMID:27040691;PMID:37876076;PMID:36273129	PCS		3/15			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:skoehler[2017-07-13];HPO:probinson[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0001500	PMID:27040691	PCS		1/13			P	HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000256	PMID:27040691;PMID:30103036;PMID:36273129;PMID:32363625	PCS		6/17			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2019-09-03];HPO:probinson[2019-09-03]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0005964	PMID:29283439	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002058	PMID:36522252	PCS		1/6			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0002059	OMIM:616900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000431	PMID:27040691;PMID:37876076;PMID:36273129	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0012510	PMID:27040692	PCS		5/5			P	HPO:probinson[2017-06-24]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000426	PMID:27040692;PMID:37876076;PMID:36273129	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-10-04];HPO:probinson[2017-06-24];HPO:probinson[2024-03-15]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000821	PMID:29283439	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0007334	PMID:32363625	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000664	PMID:27040691;PMID:37876076;PMID:36273129	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000028	PMID:36273129;PMID:36522252	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-10-04];ORCID:0000-0002-0736-9199[2024-10-14]
OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		HP:0000303	PMID:27040691;PMID:36273129	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-10-04]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001410	OMIM:614871	TAS					P	HPO:probinson[2013-02-24]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001272	PMID:20695019;PMID:19127411	PCS		3/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0003693	PMID:20695019	PCS		1/2			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002066	PMID:20695019;PMID:19127411	PCS		2/3			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001252	PMID:19127411	PCS		1/1			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001251	PMID:20695019;PMID:19127411	PCS		3/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0012569	PMID:19127411	PCS		1/1			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002080	OMIM:614871	TAS		HP:0040283			P	HPO:skoehler[2015-01-28]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0000639	PMID:19127411	PCS		1/1			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0011463	PMID:20695019;PMID:19127411	PCS		2/3			C	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0010571	PMID:20695019	PCS		4/4			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0007002	PMID:20695019	PCS		2/2			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002936	OMIM:614871	TAS		HP:0040283			P	HPO:skoehler[2015-01-28]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002317	PMID:19127411	PCS		1/1			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002415	PMID:19127411	PCS		1/1			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0006579	PMID:20695019	PCS		1/2			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0000556	OMIM:614871	TAS					P	HPO:probinson[2013-02-24]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001265	OMIM:614871	TAS		HP:0040283			P	HPO:skoehler[2015-01-28]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0003621	PMID:20695019	PCS		1/2			C	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001761	PMID:20695019	PCS		1/2			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001260	PMID:20695019;PMID:19127411	PCS		2/3			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002495	PMID:20695019	PCS		1/2			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001263	OMIM:614871	TAS					P	HPO:probinson[2013-02-24]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001284	PMID:20695019	PCS		1/2			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002070	PMID:20695019	PCS		1/2			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0000407	OMIM:614871	TAS					P	HPO:probinson[2013-02-24]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0007772	PMID:20695019	PCS		1/2			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0000007	PMID:9683594	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0001319	OMIM:614871	TAS					P	HPO:probinson[2013-02-24]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0000505	OMIM:614871	TAS					P	HPO:probinson[2013-02-24]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0003438	PMID:20695019	PCS		1/2			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0000641	PMID:19127411	PCS		1/1			P	HPO:skoehler[2015-01-28];HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0006886	PMID:20695019	PCS		1/2			P	HPO:probinson[2022-11-01]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0002500	OMIM:614871	TAS		HP:0040283			P	HPO:skoehler[2015-01-28]
OMIM:614871	Peroxisome biogenesis disorder 6B		HP:0003677	OMIM:614871	TAS					C	HPO:skoehler[2015-12-30]
OMIM:618093	Spinocerebellar ataxia 48		HP:0002069	PMID:31126790	PCS		3/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0003676	PMID:30381368	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0002015	PMID:31126790;PMID:30381368	PCS		10/17			P	HPO:probinson[2021-06-21];HPO:skoehler[2019-04-18];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001300	PMID:31126790	PCS		5/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001310	PMID:31126790	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0003487	PMID:30381368	PCS		1/9			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001332	PMID:31126790	PCS		3/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001272	PMID:31126790;PMID:30381368	PCS		11/17			P	HPO:probinson[2021-06-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001260	PMID:31126790;PMID:30381368	PCS		14/17			P	HPO:probinson[2021-06-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0002066	PMID:31126790	PCS		2/8			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0000020	PMID:30381368	PCS		3/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0003581	PMID:31126790;PMID:30381368	PCS		16/17			C	HPO:probinson[2021-06-21];HPO:probinson[2021-06-21];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001251	PMID:31126790	PCS		8/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0002072	PMID:31126790	PCS		4/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0100785	PMID:31126790	PCS					P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0000716	PMID:31126790	PCS		8/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0000737	PMID:31126790	PCS					P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0000739	PMID:31126790;PMID:30381368	PCS		15/19			P	HPO:probinson[2021-06-21];HPO:skoehler[2019-02-15];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001268	PMID:31126790	PCS		8/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0000006	PMID:30381368	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001337	PMID:31126790	PCS		2/8			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0004326	PMID:30381368	PCS		2/9			P	HPO:probinson[2021-06-21]
OMIM:618093	Spinocerebellar ataxia 48		HP:0001347	PMID:31126790	PCS		6/8			P	HPO:probinson[2021-06-21]
OMIM:101000	Neurofibromatosis, type II		HP:0007935	PMID:8318482	PCS		36/45			P	HPO:probinson[2017-12-10]
OMIM:101000	Neurofibromatosis, type II		HP:0000365	PMID:1484939	PCS		68/183		HP:0012833	P	HPO:probinson[2017-12-10];HPO:probinson[2024-03-06];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0002321	PMID:1484939	PCS		8/100			P	HPO:iea[2018-03-13];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0001250	PMID:1484939	PCS		10/120			P	HPO:probinson[2017-12-10]
OMIM:101000	Neurofibromatosis, type II		HP:0001251	PMID:1484939	PCS		10/120			P	HPO:probinson[2017-12-10]
OMIM:101000	Neurofibromatosis, type II		HP:0000360	PMID:1484939	PCS		19/183			P	HPO:probinson[2017-12-10];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0100014	PMID:1484939	PCS		1/63			P	HPO:skoehler[2013-05-31];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0000518	PMID:1484939	PCS		81/148			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0000957	PMID:1484939;PMID:19545378	PCS		158/355			P	HPO:probinson[2024-03-06];HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:101000	Neurofibromatosis, type II		HP:0011462	PMID:19545378	PCS					C	HPO:probinson[2022-03-15]
OMIM:101000	Neurofibromatosis, type II		HP:0002858	PMID:8727812;PMID:1484939;PMID:19545378	PCS		179/415			P	HPO:probinson[2024-03-06];HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:101000	Neurofibromatosis, type II		HP:0009588	PMID:1484939	PCS		62/63			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0000997	PMID:1484939	PCS		0/100			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0009589	PMID:8727812	PCS		43/48			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0002315	PMID:1484939	PCS		2/63			P	HPO:iea[2009-02-17]
OMIM:101000	Neurofibromatosis, type II		HP:0500089	PMID:1484939;PMID:19545378	PCS		15/294			P	HPO:probinson[2024-03-06];HPO:probinson[2022-03-15]
OMIM:101000	Neurofibromatosis, type II		HP:0007787	PMID:8727812	PCS		30/48			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0000751	PMID:1484939	PCS		1/63			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0001067	PMID:1484939	PCS		27/100			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0000572	PMID:1484939	PCS		7/63			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0000651	PMID:1484939	PCS		1/63			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0009590	PMID:8727812;PMID:7747758	PCS		65/111			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0009593	PMID:31881415	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0009592	PMID:1484939	PCS		1/63			P	HPO:iea[2009-02-17]
OMIM:101000	Neurofibromatosis, type II		HP:0009594	PMID:7747758	PCS		5/58			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0100019	PMID:8318482	PCS	HP:0003621	17/45			P	HPO:probinson[2017-12-10]
OMIM:101000	Neurofibromatosis, type II		HP:0009830	PMID:1484939	PCS		3/100			P	HPO:skoehler[2013-05-03];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0030052	PMID:1484939	PCS		0/100			P	HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0002888	PMID:1484939;PMID:19545378	PCS		10/294			P	HPO:probinson[2024-03-06];HPO:iea[2009-02-17];HPO:probinson[2022-03-15]
OMIM:101000	Neurofibromatosis, type II		HP:0000006	PMID:1484939	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-03-06]
OMIM:101000	Neurofibromatosis, type II		HP:0009737	PMID:1484939	PCS		2/55			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-06]
OMIM:618078	Ovarian dysgenesis 6		HP:0003621	PMID:26485283	PCS		5/5	FEMALE		C	HPO:probinson[2023-02-12]
OMIM:618078	Ovarian dysgenesis 6		HP:0000013	PMID:26485283	PCS		5/5	FEMALE		P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:618078	Ovarian dysgenesis 6		HP:0000815	PMID:26485283	PCS		5/5	FEMALE		P	HPO:probinson[2023-02-12]
OMIM:618078	Ovarian dysgenesis 6		HP:0008197	PMID:26485283	PCS		5/5	FEMALE		P	HPO:probinson[2023-02-12]
OMIM:618078	Ovarian dysgenesis 6		HP:0000007	PMID:26485283	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:618078	Ovarian dysgenesis 6		HP:0000786	PMID:26485283	PCS		5/5	FEMALE		P	HPO:probinson[2023-02-12]
OMIM:619366	Angioedema, hereditary, 7		HP:0100665	PMID:32542751	PCS		3/3		HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619366	Angioedema, hereditary, 7		HP:0033250	PMID:32542751	PCS					P	HPO:probinson[2021-07-13]
OMIM:619366	Angioedema, hereditary, 7		HP:0000282	PMID:32542751	PCS		3/3		HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619366	Angioedema, hereditary, 7		HP:0030254	PMID:32542751	PCS					P	HPO:probinson[2021-07-13]
OMIM:619366	Angioedema, hereditary, 7		HP:0031244	PMID:32542751	PCS		3/3		HP:0031796	P	HPO:probinson[2021-07-13]
OMIM:619366	Angioedema, hereditary, 7		HP:0000006	PMID:32542751	TAS					I	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:185300	Sturge-Weber syndrome		HP:0012222	OMIM:185300	TAS					P	HPO:probinson[2013-03-30]
OMIM:185300	Sturge-Weber syndrome		HP:0001250	OMIM:185300	IEA					P	HPO:iea[2009-02-17]
OMIM:185300	Sturge-Weber syndrome		HP:0002120	OMIM:185300	IEA					P	HPO:iea[2009-02-17]
OMIM:185300	Sturge-Weber syndrome		HP:0000557	OMIM:185300	IEA					P	HPO:iea[2009-02-17]
OMIM:185300	Sturge-Weber syndrome		HP:0007872	OMIM:185300	IEA					P	HPO:iea[2009-02-17]
OMIM:185300	Sturge-Weber syndrome		HP:0000329	OMIM:185300	IEA					P	HPO:iea[2009-02-17]
OMIM:185300	Sturge-Weber syndrome		HP:0003745	OMIM:185300	IEA					I	HPO:iea[2009-02-17]
OMIM:185300	Sturge-Weber syndrome		HP:0000256	OMIM:185300	TAS					P	HPO:probinson[2009-02-17]
OMIM:185300	Sturge-Weber syndrome		HP:0001249	OMIM:185300	IEA					P	HPO:iea[2009-02-17]
OMIM:616055	Episodic ataxia, type 8		HP:0002411	OMIM:616055	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:616055	Episodic ataxia, type 8		HP:0000639	OMIM:616055	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:616055	Episodic ataxia, type 8		HP:0002131	OMIM:616055	IEA					P	HPO:skoehler[2015-01-27]
OMIM:616055	Episodic ataxia, type 8		HP:0001260	OMIM:616055	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616055	Episodic ataxia, type 8		HP:0003680	OMIM:616055	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616055	Episodic ataxia, type 8		HP:0001251	OMIM:616055	TAS				HP:0025303	P	HPO:skoehler[2014-11-26]
OMIM:616055	Episodic ataxia, type 8		HP:0001350	OMIM:616055	TAS				HP:0025303	P	HPO:skoehler[2014-11-26]
OMIM:616055	Episodic ataxia, type 8		HP:0001324	OMIM:616055	TAS				HP:0025303	P	HPO:skoehler[2014-11-26]
OMIM:616055	Episodic ataxia, type 8		HP:0002080	OMIM:616055	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:616055	Episodic ataxia, type 8		HP:0000006	OMIM:616055	TAS					I	HPO:skoehler[2015-12-30]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0002421	PMID:18571143	PCS		10/10			P	HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0000486	PMID:18571143	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0003487	PMID:18571143	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0001266	PMID:18571143	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0001371	PMID:18571143	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0001250	PMID:18571143	PCS		6/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0001263	PMID:18571143	PCS		10/10			P	HPO:skoehler[2012-10-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0001252	PMID:18571143	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0002151	PMID:18571143	PCS		4/10			P	HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0005484	PMID:18571143	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0002191	PMID:18571143	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0000639	PMID:18571143	PCS		9/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0000007	PMID:18571143	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0008872	PMID:18571143	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0003219	PMID:18571143	PCS		5/8			P	HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0001258	PMID:18571143	PCS		10/10			P	HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0002415	PMID:18571143	PCS		8/8			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0002104	PMID:18571143	PCS		6/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0002599	PMID:18571143	PCS		10/10			P	HPO:probinson[2023-02-12]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0001347	PMID:18571143	PCS		10/10			P	HPO:iea[2009-02-17]
OMIM:612233	Leukodystrophy, hypomyelinating, 4		HP:0003623	PMID:18571143	PCS		10/10			C	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0002366	OMIM:105500	TAS					P	HPO:probinson[2009-02-17]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0002059	PMID:22637429	PCS		1/3			P	HPO:probinson[2023-03-08]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0001300	PMID:22637429	PCS		0/3			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-08]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0003596	PMID:22637429	PCS		1/3			C	HPO:probinson[2023-03-08]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0001283	OMIM:105500	TAS					P	HPO:probinson[2009-02-17]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0000726	PMID:22637429	PCS		1/3			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-08]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0003584	PMID:22637429	PCS		2/3			C	HPO:probinson[2023-03-08]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0003394	OMIM:105500	IEA					P	HPO:probinson[2009-02-17]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0007354	PMID:22637429	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-08]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0003470	OMIM:105500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0001324	OMIM:105500	IEA					P	HPO:skoehler[2010-06-18]
OMIM:105500	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1		HP:0000006	PMID:22637429	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-08]
OMIM:181600	Huriez syndrome		HP:0001792	OMIM:181600	TAS					P	HPO:iea[2009-02-17]
OMIM:181600	Huriez syndrome		HP:0006739	PMID:29409814	PCS		15%			P	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:181600	Huriez syndrome		HP:0025092	OMIM:181600	TAS					P	HPO:skoehler[2019-04-18]
OMIM:181600	Huriez syndrome		HP:0001182	OMIM:181600	TAS					P	HPO:skoehler[2019-04-18]
OMIM:181600	Huriez syndrome		HP:0007455	PMID:29409814	PCS					P	HPO:probinson[2021-05-02]
OMIM:181600	Huriez syndrome		HP:0007545	PMID:29409814	IEA	HP:0003577				P	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:181600	Huriez syndrome		HP:0008404	PMID:29409814	PCS					P	HPO:probinson[2021-05-02]
OMIM:181600	Huriez syndrome		HP:0000006	PMID:29409814	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:612555	Breast-Ovarian cancer, familial, susceptibility to, 2		HP:0003002	PMID:8524414	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-06]
OMIM:612555	Breast-Ovarian cancer, familial, susceptibility to, 2		HP:0100615	PMID:8524414	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-06]
OMIM:612555	Breast-Ovarian cancer, familial, susceptibility to, 2		HP:0011462	PMID:8524414	PCS					C	HPO:probinson[2023-03-06]
OMIM:612555	Breast-Ovarian cancer, familial, susceptibility to, 2		HP:0000006	PMID:8524414	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-06]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0003577	OMIM:616733	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0000365	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0002089	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001371	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001271	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001252	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001290	OMIM:616733	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001270	OMIM:616733	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0012531	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0008897	OMIM:616733	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001324	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0000110	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001562	OMIM:616733	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0011968	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0002098	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001263	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0011096	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001518	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0000822	OMIM:616733	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0000007	PMID:26084283	PCS					I	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001712	OMIM:616733	IEA					P	HPO:skoehler[2019-09-07]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0000505	OMIM:616733	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0001511	OMIM:616733	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0003259	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:616733	Coenzyme Q10 deficiency, primary, 8		HP:0005932	PMID:26084283	PCS					P	HPO:probinson[2017-06-17]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0003577	PMID:11050632	PCS		7/7			C	HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0000662	PMID:11050632	PCS		7/7			P	HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0000089	PMID:7987310	PCS		1/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0001156	OMIM:600151	TAS					P	HPO:skoehler[2014-11-26]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0001263	PMID:8588586	PCS		12/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0003241	PMID:8588586	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0000580	PMID:11050632	PCS		7/7			P	HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0005180	PMID:7987310	PCS		1/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0100259	PMID:11050632;PMID:7987310;PMID:8588586	PCS		31/31			P	HPO:probinson[2021-01-07];HPO:probinson[2021-01-07];HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0000007	PMID:15258860	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2019-02-03]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0000505	PMID:11050632	PCS		7/7			P	HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0000510	PMID:8588586	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0001513	PMID:11050632;PMID:7987310;PMID:8588586	TAS		23/31			P	HPO:probinson[2021-01-07];HPO:skoehler[2014-11-26];HPO:probinson[2021-01-07]
OMIM:600151	Bardet-Biedl syndrome 3		HP:0001249	PMID:11050632;PMID:8588586	PCS		13/19			P	HPO:probinson[2021-01-07];HPO:skoehler[2014-11-26];HPO:probinson[2021-01-07]
OMIM:620281	Deafness, autosomal dominant 87		HP:0003577	PMID:33358777	PCS		7/7			C	HPO:probinson[2023-06-25]
OMIM:620281	Deafness, autosomal dominant 87		HP:0000376	PMID:33358777	PCS		3/3			P	HPO:probinson[2023-06-25]
OMIM:620281	Deafness, autosomal dominant 87		HP:0000365	PMID:33358777	PCS		7/7		HP:0012829	P	HPO:probinson[2023-06-25]
OMIM:620281	Deafness, autosomal dominant 87		HP:0011387	PMID:33358777	PCS		3/3			P	HPO:probinson[2023-06-25]
OMIM:620281	Deafness, autosomal dominant 87		HP:0000006	PMID:33358777	PCS					I	HPO:probinson[2023-06-18]
OMIM:120970	Cone-Rod dystrophy 2		HP:0001133	PMID:9610810	PCS		7/7			P	HPO:probinson[2015-07-20];HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0011509	PMID:24136862	PCS		7/7			P	HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0007737	PMID:15531334	PCS		1/1			P	HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000662	PMID:7864751	PCS	HP:0011462				P	HPO:probinson[2009-02-17];HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000551	PMID:9610810	PCS	HP:0003621	7/7			P	HPO:skoehler[2015-07-20];HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0012508	PMID:15531334	PCS		1/1			P	HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000618	OMIM:120970	TAS					P	HPO:skoehler[2010-06-20]
OMIM:120970	Cone-Rod dystrophy 2		HP:0007663	PMID:9610810	PCS	HP:0003621	7/7			P	HPO:probinson[2015-07-20];HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0007994	OMIM:120970	TAS					P	HPO:skoehler[2015-07-26]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000548	PMID:9610810	PCS					P	HPO:probinson[2009-02-17];HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000603	PMID:7864751	PCS					P	HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0007722	PMID:15531334	PCS		1/1			P	HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000006	PMID:9610810	PCS					I	HPO:probinson[2009-02-17];HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000512	PMID:24136862	PCS					P	HP:probinson[2019-03-09]
OMIM:120970	Cone-Rod dystrophy 2		HP:0000533	OMIM:120970	TAS					P	HPO:probinson[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0001287	OMIM:600145	IEA					P	HPO:iea[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0000011	OMIM:600145	TAS					P	HPO:iea[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0003577	PMID:17409324	PCS		3/3			C	HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0002144	PMID:17409324	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0002475	PMID:17409324	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0005224	OMIM:600145	IEA					P	HPO:iea[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0025247	OMIM:600145	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600145	Sacral defect with anterior meningocele		HP:0030708	PMID:17409324	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0010305	OMIM:600145	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600145	Sacral defect with anterior meningocele		HP:0012033	OMIM:600145	TAS					P	HPO:probinson[2012-07-27]
OMIM:600145	Sacral defect with anterior meningocele		HP:0007293	OMIM:600145	TAS					P	HPO:iea[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0100565	PMID:17409324	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0009790	OMIM:600145	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600145	Sacral defect with anterior meningocele		HP:0000238	PMID:17409324	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0003418	OMIM:600145	IEA					P	HPO:iea[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0020223	PMID:17409324	PCS		1/4			P	HPO:probinson[2022-10-06]
OMIM:600145	Sacral defect with anterior meningocele		HP:0002315	OMIM:600145	IEA					P	HPO:iea[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0002019	OMIM:600145	IEA					P	HPO:iea[2009-02-17]
OMIM:600145	Sacral defect with anterior meningocele		HP:0000006	PMID:17409324	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0001776	PMID:17409324	PCS		1/4			P	HPO:probinson[2022-10-02]
OMIM:600145	Sacral defect with anterior meningocele		HP:0002435	OMIM:600145	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600145	Sacral defect with anterior meningocele		HP:0000016	OMIM:600145	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617439	Craniosynostosis 7		HP:0001363	OMIM:617439	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617439	Craniosynostosis 7		HP:0000750	OMIM:617439	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617439	Craniosynostosis 7		HP:0012758	OMIM:617439	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617439	Craniosynostosis 7		HP:0000006	OMIM:617439	TAS					I	HPO:skoehler[2017-07-13]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000483	OMIM:610356	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000662	PMID:16909397	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000486	OMIM:610356	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000613	OMIM:610356	TAS					P	HPO:skoehler[2012-10-17]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000007	PMID:16909397	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-11-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0007663	PMID:16909397	PCS					P	HPO:probinson[2022-11-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000548	PMID:16909397	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0007401	PMID:16909397	PCS		HP:0040283			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000575	OMIM:610356	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000666	OMIM:610356	TAS					P	HPO:skoehler[2013-01-22]
OMIM:610356	Retinal cone dystrophy 3B		HP:0000545	OMIM:610356	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613887	Cataract, autosomal recessive congenital 4		HP:0000518	OMIM:613887	TAS	HP:0003577				P	HPO:probinson[2013-08-10]
OMIM:613887	Cataract, autosomal recessive congenital 4		HP:0000007	OMIM:613887	TAS					I	HPO:probinson[2013-08-10]
OMIM:236600	Hydrocephalus, nonsyndromic, autosomal recessive 1		HP:0001250	PMID:21031079	PCS		1/1			P	HPO:skoehler[2013-06-05];HPO:probinson[2023-02-17]
OMIM:236600	Hydrocephalus, nonsyndromic, autosomal recessive 1		HP:0034198	PMID:21031079	PCS		2/2			C	HPO:probinson[2023-02-17]
OMIM:236600	Hydrocephalus, nonsyndromic, autosomal recessive 1		HP:0000238	PMID:21031079	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:236600	Hydrocephalus, nonsyndromic, autosomal recessive 1		HP:0000007	PMID:21031079	PCS					I	HPO:skoehler[2013-06-05];HPO:probinson[2023-02-17]
OMIM:236600	Hydrocephalus, nonsyndromic, autosomal recessive 1		HP:0002119	PMID:21031079	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-17]
OMIM:236600	Hydrocephalus, nonsyndromic, autosomal recessive 1		HP:0001249	OMIM:236600	TAS					P	HPO:skoehler[2013-06-05]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000365	OMIM:612541	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002783	PMID:19118303	PCS		2/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0003198	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0032435	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0012311	OMIM:612541	TAS					P	HPO:skoehler[2013-08-18]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0100525	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002619	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0100806	PMID:19118303	PCS		2/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000954	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001888	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001643	PMID:19118303	PCS		1/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0009789	PMID:19118303	PCS		2/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001642	PMID:19118303	PCS		1/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0003623	PMID:19118303	PCS					C	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000175	PMID:19118303	PCS		1/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000252	PMID:19118303	PCS		2/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000010	PMID:19118303	PCS		4/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001263	OMIM:612541	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0040187	PMID:19118303	PCS		5/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000407	PMID:19118303	PCS		2/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000007	PMID:19118303	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000768	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002788	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001653	PMID:19118303	PCS		1/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001015	PMID:19118303	PCS		9/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000126	OMIM:612541	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000023	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002240	OMIM:612541	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0012133	OMIM:612541	TAS					P	HPO:skoehler[2013-06-13]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001508	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001903	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002718	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000778	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0030084	OMIM:612541	TAS					P	HPO:skoehler[2014-09-21]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000218	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0012490	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001744	OMIM:612541	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0004854	PMID:19118303	PCS		5/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000431	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001882	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000155	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001684	PMID:19118303	PCS		7/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0010774	PMID:19118303	PCS		1/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002092	OMIM:612541	TAS					P	HPO:skoehler[2015-01-21]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002093	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0011304	OMIM:612541	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0002205	OMIM:612541	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001510	OMIM:612541	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001433	PMID:19118303	PCS		3/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000388	PMID:19118303	PCS		1/12			P	HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001873	OMIM:612541	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0000028	PMID:19118303	PCS		4/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11]
OMIM:612541	Neutropenia, severe congenital, 4, autosomal recessive		HP:0001875	PMID:19118303	PCS		12/12			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-11]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0002960	OMIM:612227	TAS					P	HPO:probinson[2009-02-17]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0000819	OMIM:612227	IEA					P	HPO:skoehler[2015-01-27]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0001993	OMIM:612227	TAS					P	HPO:probinson[2009-02-17]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0000855	OMIM:612227	TAS					P	HPO:probinson[2009-02-17]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0001426	OMIM:612227	TAS					I	HPO:probinson[2009-02-17]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0000007	OMIM:612227	IEA					I	HPO:skoehler[2018-10-08]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0006279	OMIM:612227	TAS					P	HPO:probinson[2009-02-17]
OMIM:612227	Diabetes mellitus, ketosis-prone		HP:0000006	OMIM:612227	TAS					I	HPO:skoehler[2015-12-30]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0002014	OMIM:615548	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0003577	PMID:24036948	PCS		2/2			C	HPO:probinson[2022-12-13]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0012332	OMIM:615548	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0001058	PMID:24036948	PCS		2/2			P	HPO:probinson[2022-12-13]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0007021	PMID:24036948	PCS		2/2			P	HPO:skoehler[2014-06-24];HPO:probinson[2022-12-13]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0000975	OMIM:615548	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0001270	PMID:24036948	PCS		2/2		HP:0012825	P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-13]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0000989	OMIM:615548	TAS					P	HPO:skoehler[2017-07-13]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0001324	PMID:24036948	PCS		2/2		HP:0012825	P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-13]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0002019	OMIM:615548	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615548	Neuropathy, hereditary sensory and autonomic, type VII		HP:0000006	PMID:24036948	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-13]
OMIM:232300	Glycogen storage disease II		HP:0003236	OMIM:232300	TAS					P	HPO:probinson[2012-04-11]
OMIM:232300	Glycogen storage disease II		HP:0002202	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0000365	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0003551	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0001252	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0000020	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0002240	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0001790	PMID:33082562;PMID:31467850	PCS		11/11			P	HPO:probinson[2025-03-01]
OMIM:232300	Glycogen storage disease II		HP:0003690	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:6001008	PMID:20301438	PCS					P	HPO:probinson[2024-08-03]
OMIM:232300	Glycogen storage disease II		HP:0033567	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0011462	PMID:35386406	PCS		1/1			C	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0006597	OMIM:232300	TAS					P	HPO:probinson[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0003725	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0001945	OMIM:232300	TAS					P	HPO:probinson[2012-04-11]
OMIM:232300	Glycogen storage disease II		HP:0025435	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0000158	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0001324	PMID:35386406	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0003701	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0001744	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0003546	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0002138	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0001265	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:6000088	OMIM:232300	TAS					P	HPO:probinson[2024-01-13]
OMIM:232300	Glycogen storage disease II		HP:0001640	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0001288	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0001284	OMIM:232300	TAS					P	HPO:probinson[2012-04-11]
OMIM:232300	Glycogen storage disease II		HP:0005165	OMIM:232300	TAS					P	HPO:probinson[2013-04-07]
OMIM:232300	Glycogen storage disease II		HP:0033235	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0002094	PMID:35386406	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0011400	OMIM:232300	TAS					P	HPO:probinson[2012-04-11]
OMIM:232300	Glycogen storage disease II		HP:0002093	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0011703	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0009051	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0031185	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0001716	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0032232	PMID:35386406	PCS		1/1			P	HPO:probinson[2022-06-15]
OMIM:232300	Glycogen storage disease II		HP:0000007	OMIM:232300	IEA					I	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0002747	OMIM:232300	TAS					P	HPO:skoehler[2013-04-07]
OMIM:232300	Glycogen storage disease II		HP:0002205	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:232300	Glycogen storage disease II		HP:0004944	OMIM:232300	IEA					P	HPO:iea[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0002894	OMIM:151623	IEA					P	HPO:iea[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0002488	OMIM:151623	IEA					P	HPO:iea[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0003002	OMIM:151623	IEA					P	HPO:iea[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0003003	OMIM:151623	IEA					P	HPO:iea[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0030078	OMIM:151623	TAS					P	HPO:skoehler[2014-09-21]
OMIM:151623	Li-Fraumeni syndrome		HP:0012125	OMIM:151623	TAS					P	HPO:skoehler[2012-10-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0030448	OMIM:151623	TAS					P	HPO:skoehler[2015-08-05]
OMIM:151623	Li-Fraumeni syndrome		HP:0100787	OMIM:151623	TAS					P	HPO:probinson[2012-07-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0100768	OMIM:151623	IEA					P	HPO:skoehler[2019-09-07]
OMIM:151623	Li-Fraumeni syndrome		HP:0002669	OMIM:151623	TAS					P	HPO:probinson[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0002667	OMIM:151623	IEA					P	HPO:iea[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0000006	OMIM:151623	IEA					I	HPO:iea[2009-02-17]
OMIM:151623	Li-Fraumeni syndrome		HP:0006744	OMIM:151623	IEA					P	HPO:iea[2009-02-17]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0002067	PMID:26475694	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0002375	OMIM:609161	IEA					P	HPO:iea[2009-02-17]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0003596	PMID:26475694;PMID:20085714	PCS		8/8			C	HPO:probinson[2023-03-18];HPO:probinson[2024-03-14]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0001288	PMID:20085714	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0002395	OMIM:609161	IEA					P	HPO:iea[2009-02-17]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0001260	PMID:26475694	PCS		1/1			P	HPO:skoehler[2009-02-17]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0002063	PMID:20085714	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0002075	PMID:20085714	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2024-03-14]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0001350	PMID:26475694	PCS		1/1			P	HPO:probinson[2023-03-18]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0040140	PMID:20085714	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2024-03-14]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0007039	PMID:26475694	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-18]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0000006	PMID:20085714	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-18]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0001348	PMID:26475694	PCS		1/1			P	HPO:probinson[2023-03-18]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0003677	PMID:26475694	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2023-03-18]
OMIM:609161	Striatal degeneration, autosomal dominant		HP:0001337	PMID:20085714	PCS		0/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2024-03-14]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000670	PMID:23851939	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0004467	PMID:23851939	PCS		4/4		HP:0012832	P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000431	PMID:23851939	PCS		2/3			P	HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000265	OMIM:615560	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000592	OMIM:615560	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615560	Otofaciocervical syndrome 2		HP:0003691	PMID:23851939	PCS		2/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0001263	PMID:23851939	PCS		3/4			P	HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0001182	OMIM:615560	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615560	Otofaciocervical syndrome 2		HP:0030668	PMID:23851939	PCS		1/4			P	HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000308	PMID:23851939	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000509	PMID:23851939	PCS		3/4			P	HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000107	PMID:23851939	PCS		2/4			P	HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000007	PMID:23851939	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000689	OMIM:615560	TAS		HP:0040283			P	HPO:skoehler[2014-01-28]
OMIM:615560	Otofaciocervical syndrome 2		HP:0030084	OMIM:615560	TAS		HP:0040283			P	HPO:skoehler[2014-09-21]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000378	PMID:23851939	PCS		4/4			P	HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0007678	PMID:23851939	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000410	PMID:23851939	PCS		4/4			P	HPO:skoehler[2014-06-24];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0200021	PMID:23851939	PCS		1/3			P	HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000369	PMID:23851939	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:615560	Otofaciocervical syndrome 2		HP:0000522	PMID:23851939	PCS		4/4			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-12]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000494	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0001792	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0005321	OMIM:608257	TAS					P	HPO:probinson[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000272	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0012385	OMIM:608257	TAS					P	HPO:skoehler[2015-12-30]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0009892	OMIM:608257	IEA					P	HPO:skoehler[2010-06-18]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0009473	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000689	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000405	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000006	OMIM:608257	IEA					I	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000347	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000402	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0000413	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:608257	Mandibulofacial dysostosis with ptosis, autosomal dominant		HP:0007911	OMIM:608257	IEA					P	HPO:iea[2009-02-17]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0003577	PMID:24691054	PCS		1/1			C	HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0001561	PMID:24691054	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0002013	OMIM:616069	TAS					P	HPO:skoehler[2014-11-26]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0003212	PMID:24691054	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0200039	PMID:24691054	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0001680	PMID:24691054	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0025092	PMID:24691054	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0100501	OMIM:616069	TAS					P	HPO:skoehler[2014-11-26]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0001508	PMID:24691054	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0001944	PMID:24691054	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0000822	PMID:24691054	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0000007	PMID:24691054	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0000527	OMIM:616069	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0200034	PMID:24691054	PCS		1/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2023-02-12]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0006532	OMIM:616069	TAS					P	HPO:skoehler[2014-11-26]
OMIM:616069	Inflammatory skin and bowel disease, neonatal, 2		HP:0005208	PMID:24691054	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:611706	Migraine with or without aura, susceptibility to, 12		HP:0002013	OMIM:611706	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611706	Migraine with or without aura, susceptibility to, 12		HP:0002076	OMIM:611706	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611706	Migraine with or without aura, susceptibility to, 12		HP:0000613	OMIM:611706	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611706	Migraine with or without aura, susceptibility to, 12		HP:0002183	OMIM:611706	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611706	Migraine with or without aura, susceptibility to, 12		HP:0002018	OMIM:611706	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611706	Migraine with or without aura, susceptibility to, 12		HP:0002315	OMIM:611706	TAS					P	HPO:skoehler[2017-07-13]
OMIM:611706	Migraine with or without aura, susceptibility to, 12		HP:0000006	OMIM:611706	TAS					I	HPO:skoehler[2017-07-13]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0025474	PMID:9036939	PCS		1/2			P	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0001595	PMID:9036939	PCS		0/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0003577	PMID:9036939	PCS		1/2			C	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0001597	PMID:9036939	PCS		0/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0010783	PMID:9036939	PCS		2/2			P	HPO:skoehler[2010-06-20]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0040162	PMID:9036939	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0008064	PMID:9036939	PCS		2/2			P	HPO:probinson[2013-12-16];HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0008066	PMID:9036939	PCS		2/2			P	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0040189	PMID:9036939	PCS		1/2			P	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0007453	PMID:9036939	PCS		1/2			P	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0007475	PMID:9036939	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0000972	PMID:9036939	PCS		0/2			P	HPO:probinson[2009-02-17];HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0000006	PMID:9036939	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0200041	PMID:9036939	PCS		2/2			P	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0003623	PMID:9036939	PCS		1/2			C	HPO:probinson[2023-04-08]
OMIM:607602	Ichthyosis, cyclic, with epidermolytic hyperkeratosis		HP:0040009	PMID:9036939	PCS		1/1			P	HPO:probinson[2023-04-08]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0000859	PMID:21311022	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-12-13]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0001959	OMIM:613677	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0003351	OMIM:613677;PMID:21311022	PCS		13/13			P	HPO:probinson[2013-06-02];HPO:probinson[2022-12-13]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0008221	OMIM:613677	TAS					P	HPO:probinson[2013-06-02]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0000822	PMID:21311022	PCS		3/3			P	HPO:probinson[2013-06-02];HPO:probinson[2022-12-13]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0002150	OMIM:613677	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0002900	OMIM:613677	TAS					P	HPO:skoehler[2014-08-03]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0000103	OMIM:613677	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0000006	PMID:21311022	PCS					I	HPO:probinson[2013-06-02];HPO:probinson[2022-12-13]
OMIM:613677	Hyperaldosteronism, familial, type III		HP:0001942	OMIM:613677	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:615206	Card11 immunodeficiency		HP:0004313	PMID:23374270	PCS		1/1			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0004432	PMID:23561803	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0003593	PMID:23374270;PMID:23561803	PCS		2/2			C	HPO:skoehler[2013-05-07];HPO:probinson[2022-11-06];HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0000007	PMID:23561803	PCS					I	HPO:skoehler[2013-05-07];HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0020102	PMID:23374270;PMID:23561803	PCS		2/2			P	HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0002205	PMID:23374270	PCS		1/1			P	HPO:skoehler[2013-05-07];HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0012312	PMID:23561803	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0031402	PMID:23561803	PCS		1/1			P	HPO:probinson[2022-11-06]
OMIM:615206	Card11 immunodeficiency		HP:0002721	PMID:23561803	PCS		1/1			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-11-06]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002069	PMID:30244534	PCS		3/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002521	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002188	PMID:30244534	PCS		2/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000343	PMID:30244534	PCS		3/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000100	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001250	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002384	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002120	PMID:30244534	PCS		1/5		HP:0012825	P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001252	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001251	PMID:30244534	PCS		2/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0033720	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0012469	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0031491	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000319	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000817	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0012450	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000954	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000733	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0025336	PMID:30244534	PCS		2/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000212	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001265	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000099	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000252	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002213	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001344	PMID:27346735;PMID:30244534	PCS		5/6			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0031936	PMID:30244534	PCS		5/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001382	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0033719	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000490	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001263	PMID:30244534	PCS		5/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000096	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000093	PMID:30244534	PCS		2/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0011344	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0007270	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002827	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0032792	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0008763	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0007334	PMID:30244534	PCS		1/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000664	PMID:30244534	PCS		2/5			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0001510	PMID:27346735	PCS		1/1			P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000047	PMID:30244534	PCS		1/2	MALE		P	HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0000006	PMID:27346735	PCS					I	HPO:probinson[2021-10-21];HPO:probinson[2021-10-21]
OMIM:619428	Focal segmental glomerulosclerosis and neurodevelopmental syndrome		HP:0002346	PMID:30244534	PCS		1/5		HP:0012825	P	HPO:probinson[2021-10-21]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0003577	PMID:26044572	PCS					C	HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0004322	PMID:26044572	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0001156	PMID:26044572	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0001162	PMID:26044572	PCS		3/7			P	HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0010454	PMID:26044572	PCS		5/7			P	HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0034374	PMID:26044572	PCS		5/7			P	HPO:probinson[2022-09-05]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0000888	PMID:26044572	PCS		5/7			P	HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0000007	PMID:26044572	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0000895	PMID:27666822	PCS					P	HPO:lccarmody[2018-09-26]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0000774	PMID:26044572	PCS		4/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0001830	PMID:26044572	PCS		4/7			P	HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0001522	PMID:26044572	PCS		1/7			C	HPO:probinson[2022-08-22]
OMIM:617405	Short-Rib thoracic dysplasia 17 with or without polydactyly		HP:0000773	PMID:26044572	PCS		5/7			P	HPO:probinson[2022-08-22]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0005469	PMID:26340333	PCS		1/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000252	PMID:26340333	PCS		3/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000494	PMID:26340333	PCS		3/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0006956	PMID:26340333	PCS		2/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0001476	PMID:26340333	PCS		2/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000486	PMID:26340333	PCS		5/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0002650	PMID:26340333	PCS		2/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0004443	PMID:26340333	PCS		1/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0003298	PMID:26340333	PCS		2/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0001274	PMID:26340333	PCS		1/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000294	PMID:26340333	PCS		1/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0011318	PMID:26340333	IEA	HP:0003577	6/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0012110	PMID:26340333	PCS		3/9			P	HPO:probinson[2020-05-20];HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000609	PMID:26340333	PCS		1/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000729	PMID:26340333	PCS		2/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000508	PMID:26340333	PCS		3/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000348	PMID:26340333	PCS		3/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0001305	PMID:26340333	PCS		1/9			P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000006	PMID:26340333	PCS					I	HPO:probinson[2020-05-20];HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000248	PMID:26340333	PCS	HP:0003577				P	HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0001249	PMID:26340333	PCS		9/9			P	HPO:probinson[2020-05-20];HPO:probinson[2020-05-20]
OMIM:618736	Structural brain anomalies with impaired intellectual development and craniosynostosis		HP:0000324	PMID:26340333	PCS					P	HPO:probinson[2020-05-20]
OMIM:607616	Niemann-pick disease, type B		HP:0003596	PMID:22818240	PCS		5/15			C	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0003233	PMID:15545621;PMID:22818240	PCS		36/44			P	HPO:probinson[2022-03-19];HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0004322	OMIM:607616	IEA					P	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0002240	PMID:22818240	PCS		10/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0045051	PMID:22818240	PCS		5/8			P	HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0011463	PMID:22818240	PCS		1/15			C	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0001903	PMID:22818240	PCS		4/15			P	HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0011462	PMID:22818240	PCS		7/15			C	HPO:probinson[2022-03-19];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0034300	OMIM:607616	TAS					P	HPO:probinson[2022-09-05]
OMIM:607616	Niemann-pick disease, type B		HP:0003609	OMIM:607616	IEA					P	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0006530	PMID:22818240	PCS		2/15			P	HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0001103	OMIM:607616	IEA					P	HPO:skoehler[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0001268	PMID:22818240	PCS		0/15			P	HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0001744	PMID:22818240	PCS		14/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0003621	PMID:22818240	PCS		2/15			C	HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0001982	OMIM:607616	IEA					P	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0002155	PMID:22818240	PCS		24/29			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0004333	OMIM:607616	IEA					P	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0003141	PMID:15545621;PMID:22818240	PCS		23/44			P	HPO:probinson[2022-03-19];HPO:iea[2009-02-17];HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0002094	OMIM:607616	IEA					P	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0002829	PMID:22818240	PCS		2/15			P	HPO:probinson[2022-03-19]
OMIM:607616	Niemann-pick disease, type B		HP:0000007	OMIM:607616	IEA					I	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0002207	OMIM:607616	IEA					P	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0002205	OMIM:607616	IEA					P	HPO:iea[2009-02-17]
OMIM:607616	Niemann-pick disease, type B		HP:0001873	PMID:22818240	PCS		8/15			P	HPO:probinson[2022-03-19]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000286	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000486	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0004322	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001250	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000160	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0003593	OMIM:618050;PMID:27479843	PCS		11/12			C	HPO:probinson[2022-05-31];HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001290	OMIM:618050	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001609	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000316	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000998	OMIM:618050	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0002019	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001763	OMIM:618050	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001249	PMID:27479843	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000358	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000252	OMIM:618050	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0011968	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001382	OMIM:618050	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001263	PMID:27479843	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0005780	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0011800	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000729	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000722	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000006	PMID:27479843	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0002883	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000582	PMID:27479843	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0003577	PMID:27479843	PCS		1/2			C	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001156	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001195	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000581	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001270	PMID:27479843	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0025161	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001508	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000739	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000219	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000218	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000455	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0002014	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0001363	OMIM:618050	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000750	PMID:27479843	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0002254	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0002650	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000276	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0400000	OMIM:618050	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0009276	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0002808	PMID:27479843	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000506	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000508	PMID:27479843	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000426	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000307	PMID:27479843	PCS		2/2			P	HPO:probinson[2022-05-31]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0030051	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0007018	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000388	OMIM:618050	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618050	Intellectual developmental disorder, autosomal dominant 57		HP:0000545	PMID:27479843	PCS		1/2			P	HPO:probinson[2022-05-31]
OMIM:615574	Asparagine synthetase deficiency		HP:0002267	OMIM:615574;PMID:27469131;PMID:24139043	PCS		14/21			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-14];HPO:probinson[2023-08-22];HPO:probinson[2023-08-22];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001298	OMIM:615574	TAS				HP:0003676	P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0003676	OMIM:615574	TAS					C	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0001176	OMIM:615574	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0001250	PMID:29375865	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0002340	PMID:27469131	PCS		1/2			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0025664	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001252	PMID:27469131	PCS		1/2			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0003593	PMID:24139043	PCS		2/6			C	HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0002020	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0033725	PMID:27469131;PMID:29375865	PCS		2/3			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0012110	PMID:27469131;PMID:28776279;PMID:24139043	PCS		8/12			P	HPO:skoehler[2014-09-21];HPO:probinson[2022-12-14];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0007082	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0000316	PMID:27469131	PCS		1/2			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002539	OMIM:615574	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0020045	PMID:28776279	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0020206	PMID:27469131	PCS		1/2			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0003623	PMID:24139043	PCS		4/6			C	HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0000253	OMIM:615574	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615574	Asparagine synthetase deficiency		HP:0002510	PMID:28776279	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0000252	PMID:24139043	PCS		8/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0002079	PMID:27469131	PCS		1/2			P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0011968	PMID:27469131	PCS		2/2			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002198	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001263	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0012736	OMIM:615574	TAS					P	HPO:probinson[2017-05-29]
OMIM:615574	Asparagine synthetase deficiency		HP:0000609	PMID:28776279	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0034197	PMID:28776279	PCS		3/3			C	HPO:probinson[2023-08-22];HPO:probinson[2023-08-22];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0011451	PMID:27469131;PMID:29375865	PCS		3/3			P	HPO:probinson[2023-08-22];HPO:probinson[2023-08-22];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002509	PMID:24139043	PCS		9/9			P	HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0000007	PMID:24139043	PCS					I	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0000400	OMIM:615574	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0001337	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0500157	PMID:28776279	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001276	PMID:27469131;PMID:29375865	PCS		3/3			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0000340	PMID:27469131;PMID:29375865	PCS		2/3			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002521	PMID:24139043	PCS		3/8			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0003577	PMID:29375865	PCS		1/1			C	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002169	PMID:27469131	PCS		1/2			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002365	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002283	PMID:28776279	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0005274	PMID:27469131	PCS		2/2			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0012448	OMIM:615574	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0001508	PMID:28776279	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0000737	PMID:28776279	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0100704	PMID:28776279	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0000618	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0020221	PMID:28776279	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0002119	PMID:27469131	PCS		2/2			P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0001347	PMID:27469131;PMID:28776279;PMID:24139043	PCS		11/12			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-14];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001320	PMID:28776279	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0008936	PMID:27469131;PMID:24139043	PCS		6/11			P	HPO:skoehler[2014-01-28];HPO:probinson[2022-12-14];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001321	PMID:29375865	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0010851	PMID:24139043	PCS		2/8			P	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0011344	PMID:24139043	PCS		9/9			P	HPO:probinson[2022-12-14]
OMIM:615574	Asparagine synthetase deficiency		HP:0002093	OMIM:615574	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0010535	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0034295	PMID:29375865	PCS		1/1			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0009110	PMID:27469131	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001833	OMIM:615574	TAS					P	HPO:skoehler[2014-05-04]
OMIM:615574	Asparagine synthetase deficiency		HP:0001558	PMID:27469131;PMID:28776279	PCS		2/3			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0001511	PMID:27469131	PCS		2/2			P	HPO:probinson[2023-08-22]
OMIM:615574	Asparagine synthetase deficiency		HP:0000347	OMIM:615574	TAS					P	HPO:skoehler[2014-01-28]
OMIM:615574	Asparagine synthetase deficiency		HP:0009879	PMID:27469131;PMID:24139043;PMID:29375865	PCS		9/12			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-14];HPO:probinson[2023-08-22]
OMIM:613105	Choroidal dystrophy, central areolar 2		HP:0000613	OMIM:613105	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613105	Choroidal dystrophy, central areolar 2		HP:0000006	OMIM:613105	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613105	Choroidal dystrophy, central areolar 2		HP:0000533	PMID:14557183	PCS					P	HPO:probinson[2015-07-19]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001176	PMID:20543202	PCS		13/28			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000486	PMID:20543202	PCS		4/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000365	PMID:20543202	PCS		3/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001250	PMID:20543202	PCS		2/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001252	PMID:20543202	PCS		13/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001290	OMIM:613675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000280	PMID:20543202	PCS		17/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0100543	PMID:20543202	PCS		27/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0007183	PMID:20543202	PCS		13/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000957	PMID:20543202	PCS		27/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000316	PMID:20543202	PCS		25/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001328	PMID:20543202	PCS		13/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001548	OMIM:613675	TAS					P	HPO:skoehler[2013-05-31]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000997	PMID:20543202	PCS		28/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0030680	PMID:20543202	PCS		8/28			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000736	PMID:20543202	PCS		16/22			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001627	OMIM:613675	TAS					P	HPO:skoehler[2015-12-30]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0003745	OMIM:613675	PCS					I	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000256	PMID:20543202	PCS		9/23			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001249	OMIM:613675	TAS		38%			P	HPO:skoehler[2012-11-18]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001067	PMID:20543202	PCS		25/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000098	PMID:20543202	PCS		13/28			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000475	PMID:20543202	PCS		9/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0002650	PMID:20543202	PCS		12/28			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000750	PMID:20543202	PCS		14/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001761	PMID:20543202	PCS		5/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001382	PMID:20543202	PCS		21/29			P	HPO:iea[2011-03-29]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0002011	PMID:20543202	PCS		5/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001263	PMID:20543202	PCS		14/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0100697	PMID:20543202	PCS		6/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0100698	PMID:20543202	PCS		22/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0012062	PMID:20543202	PCS		8/16			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000767	PMID:20543202	PCS		9/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0001833	OMIM:613675	TAS		46%			P	HPO:skoehler[2012-11-18]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0030052	OMIM:613675	TAS					P	HPO:skoehler[2014-09-21]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0009732	PMID:20543202	PCS		22/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0009735	PMID:20543202	PCS		9/14			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0007018	PMID:20543202	PCS		8/24			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0009734	PMID:20543202	PCS		5/27			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0009737	PMID:20543202	PCS		27/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000369	PMID:20543202	PCS		4/29			P	HPO:iea[2012-04-24]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000006	OMIM:613675	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613675	Chromosome 17q11.2 deletion syndrome, 1.4-mb		HP:0000324	PMID:20543202	PCS		8/29			P	HPO:iea[2012-04-24]
OMIM:156600	Microcoria, congenital		HP:0000616	OMIM:156600	TAS					P	HPO:probinson[2009-02-17]
OMIM:156600	Microcoria, congenital		HP:0007906	OMIM:156600	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:156600	Microcoria, congenital		HP:0008345	OMIM:156600	IEA					P	HPO:iea[2009-02-17]
OMIM:156600	Microcoria, congenital		HP:0025492	OMIM:156600	TAS	HP:0003577				P	HPO:skoehler[2017-07-13]
OMIM:156600	Microcoria, congenital		HP:0000006	OMIM:156600	IEA					I	HPO:iea[2009-02-17]
OMIM:156600	Microcoria, congenital		HP:0000545	OMIM:156600	IEA					P	HPO:iea[2009-02-17]
OMIM:156600	Microcoria, congenital		HP:0000501	OMIM:156600	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:613107	Neutropenia, severe congenital, 2, autosomal dominant		HP:0012311	OMIM:613107	TAS					P	HPO:probinson[2013-08-10]
OMIM:613107	Neutropenia, severe congenital, 2, autosomal dominant		HP:0010976	OMIM:613107	TAS					P	HPO:probinson[2013-06-02]
OMIM:613107	Neutropenia, severe congenital, 2, autosomal dominant		HP:0000006	OMIM:613107	TAS					I	HPO:probinson[2013-06-02]
OMIM:613107	Neutropenia, severe congenital, 2, autosomal dominant		HP:0001875	OMIM:613107	TAS					P	HPO:probinson[2013-06-02]
OMIM:261000	Intrinsic factor deficiency		HP:0020181	PMID:14576042	PCS		1/1			P	HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0003401	OMIM:261000	IEA					P	HPO:iea[2009-02-17]
OMIM:261000	Intrinsic factor deficiency		HP:0003621	OMIM:261000	IEA					C	HPO:iea[2009-02-17]
OMIM:261000	Intrinsic factor deficiency		HP:0200118	PMID:14576042	PCS		1/1			P	HPO:skoehler[2013-06-11];HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0003474	OMIM:261000	IEA					P	HPO:iea[2009-02-17]
OMIM:261000	Intrinsic factor deficiency		HP:0031965	PMID:14576042	PCS		1/1			P	HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0100502	PMID:14576042	PCS		1/1			P	HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0011463	PMID:14576042	PCS		1/1			C	HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0001889	PMID:14576042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0000007	PMID:14576042	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0005518	OMIM:261000	IEA					P	HPO:iea[2009-02-17]
OMIM:261000	Intrinsic factor deficiency		HP:0025435	PMID:14576042	PCS		1/1			P	HPO:probinson[2022-10-22]
OMIM:261000	Intrinsic factor deficiency		HP:0200143	OMIM:261000	TAS					P	HPO:skoehler[2013-06-13]
OMIM:261000	Intrinsic factor deficiency		HP:0005219	PMID:14576042	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-22]
OMIM:530000	Kearns-Sayre syndrome		HP:0004322	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001250	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000580	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001251	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0011675	OMIM:530000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:530000	Kearns-Sayre syndrome		HP:0000819	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001709	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001947	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001427	OMIM:530000	IEA					I	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001924	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001324	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0003128	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0002135	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000252	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0003200	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000590	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000829	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000407	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000726	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000508	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001638	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0002922	OMIM:530000	TAS					P	HPO:probinson[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0000763	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0001994	OMIM:530000	TAS					P	HPO:probinson[2009-02-17]
OMIM:530000	Kearns-Sayre syndrome		HP:0008207	OMIM:530000	IEA					P	HPO:iea[2009-02-17]
OMIM:612219	Ewing sarcoma		HP:0012254	OMIM:612219	TAS					P	HPO:probinson[2013-01-09]
OMIM:612219	Ewing sarcoma		HP:0001442	OMIM:612219	TAS					I	HPO:probinson[2013-04-07]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0003577	PMID:26846950	PCS		2/5			C	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0031319	PMID:26846950	PCS		1/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001640	PMID:26846950	PCS		3/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001695	PMID:26846950	PCS		1/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0005157	PMID:26846950	PCS		2/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0005144	PMID:26846950;PMID:27106955	PCS		3/7			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0025168	PMID:26846950	PCS		1/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001790	PMID:26846950	PCS		2/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0003593	PMID:27106955	PCS		2/2			C	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0005180	PMID:26846950	PCS		2/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0034197	PMID:26846950	PCS		1/5			C	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001706	PMID:26846950	PCS		1/1			P	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0034198	PMID:26846950	PCS		1/5			C	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001639	PMID:26846950;PMID:27106955	PCS		3/7			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0011463	PMID:26846950	PCS		1/5			C	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0006670	PMID:26846950	PCS		2/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001657	PMID:27106955	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001635	PMID:26846950	PCS		1/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0000007	PMID:26846950	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0002119	PMID:26846950	PCS		1/5			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001653	PMID:26846950	PCS		1/5			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001059	PMID:27106955	PCS		2/2			P	HPO:probinson[2022-07-11]
OMIM:618052	Cardiomyopathy, familial hypertrophic 27		HP:0001667	PMID:26846950	PCS		1/5			P	HPO:probinson[2022-07-11]
OMIM:265500	Pulmonic stenosis		HP:0000007	OMIM:265500	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:265500	Pulmonic stenosis		HP:0001426	PMID:12987021	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:265500	Pulmonic stenosis		HP:0001642	OMIM:265500	IEA					P	HPO:iea[2009-02-17]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0005313	PMID:27895300	PCS		2/17			P	HPO:probinson[2021-07-13]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0003596	PMID:27895300	PCS		14/17			C	HPO:probinson[2021-07-13]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0003584	PMID:27895300	PCS		3/17			C	HPO:probinson[2021-07-13]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0031056	PMID:27895300	PCS		3/17			P	HPO:probinson[2021-07-13]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0007029	PMID:27895300	IEA		14/17			P	HPO:probinson[2021-07-13]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0012159	PMID:27895300	PCS		1/17			P	HPO:probinson[2021-07-16]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0000006	PMID:27895300	PCS					I	HPO:probinson[2021-07-13];HPO:probinson[2021-07-13]
OMIM:618734	Aneurysm, intracranial berry, 12		HP:0002138	PMID:27895300	PCS		7/17			P	HPO:probinson[2021-07-13]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001399	OMIM:616719	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0002066	PMID:26581903	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0025268	PMID:26581903	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001395	PMID:26581903	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0002240	PMID:26581903	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0003593	PMID:26581903	PCS		2/3			C	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0002460	PMID:26581903	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001270	PMID:26581903	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0007141	PMID:26581903	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0011463	PMID:26581903	PCS		1/3			C	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0002936	PMID:26581903	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0002359	PMID:26581903	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001744	PMID:26581903	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001347	PMID:26581903	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0007328	PMID:26581903	PCS		1/3			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0006855	PMID:26581903	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001265	PMID:26581903	PCS		2/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0003202	PMID:26581903	PCS		3/3			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0003401	PMID:26581903	PCS		1/3			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001762	OMIM:616719	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0002070	PMID:26581903	PCS		1/3			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0012852	PMID:26581903	PCS		2/2			P	HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0000007	PMID:26581903	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001257	PMID:26581903	PCS		1/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:616719	Spinocerebellar ataxia, autosomal recessive 21		HP:0001337	PMID:26581903	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-04]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0003431	PMID:27797808	PCS		40/43			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001250	PMID:27797808	PCS		6/57			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0003474	PMID:27797808	PCS					P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0002063	PMID:27797808	PCS		10/56			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0000020	PMID:27797808	PCS		22/52			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001251	PMID:27797808	PCS		20/56			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0012229	PMID:27797808	PCS		5/39			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0100543	PMID:27797808	PCS		18/41			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0007185	PMID:27797808	PCS		20/57			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0000616	PMID:27797808	PCS		24/39			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0002119	PMID:27797808	PCS		47/51			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001324	PMID:27797808	PCS		28/56			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0003448	PMID:27797808	PCS		33/43			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0003403	PMID:27797808	PCS		11/42			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001265	PMID:27797808	PCS					P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001288	PMID:27797808	PCS					P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001260	PMID:27797808	PCS		2/57			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0002352	PMID:27797808	PCS		47/51			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0002572	PMID:27797808	PCS		12/57			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0000708	PMID:27797808	PCS		12/56			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0000726	PMID:27797808	PCS		45/57			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0002922	PMID:27797808	PCS		23/39			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001279	PMID:27797808	PCS		3/57			P	HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0000006	PMID:27797808	PCS					I	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:603472	Neuronal intranuclear inclusion disease		HP:0001337	PMID:27797808	PCS		12/57			P	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0002179	PMID:20080937	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0003642	PMID:20080937	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0000252	PMID:20080937	PCS		1/2			P	HPO:skoehler[2015-07-26];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0001344	OMIM:613661	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0000486	OMIM:613661	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0002013	PMID:20080937	PCS		2/2		HP:0031796	P	HPO:skoehler[2013-06-11];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0011968	PMID:20080937	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0001250	PMID:20080937	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0001263	OMIM:613661	TAS		20/20			P	HPO:skoehler[2019-02-22];HPO:skoehler[2012-10-17]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0001252	PMID:20080937	PCS		2/2			P	HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0003593	PMID:20080937	PCS		1/2			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0003186	PMID:20080937	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0000294	PMID:20080937	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0003819	PMID:20080937	PCS		1/2			C	HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0000407	PMID:20080937	PCS		2/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0011198	PMID:20080937	PCS		2/2			P	HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0000007	PMID:20080937	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0000348	PMID:20080937	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0001987	PMID:20080937	PCS		1/2			P	HPO:probinson[2023-01-26]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0001319	OMIM:613661	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0005968	OMIM:613661	TAS					P	HPO:skoehler[2013-06-04]
OMIM:613661	Congenital disorder of glycosylation, type Ip		HP:0003623	PMID:20080937	PCS		1/2			C	HPO:probinson[2023-01-26]
OMIM:620283	Deafness, autosomal dominant 88		HP:0000365	PMID:36048850	PCS					P	HPO:probinson[2023-06-25]
OMIM:620283	Deafness, autosomal dominant 88		HP:0011462	PMID:36048850	PCS					C	HPO:probinson[2023-06-25]
OMIM:620283	Deafness, autosomal dominant 88		HP:0000006	PMID:36048850	PCS					I	HPO:probinson[2023-06-25]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0001297	PMID:30442288	PCS		5/64			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0005157	PMID:30442288	PCS		4/41			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0001670	PMID:30442288	PCS		35/41			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0003581	PMID:30442288	PCS					C	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0005110	PMID:30442288	PCS		6/55			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0031992	PMID:30442288	PCS		2/41			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0012664	PMID:30442288	PCS		6/46			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0031656	PMID:30442288	PCS		5/40			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:4000004	PMID:30442288	PCS		11/17			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0031295	PMID:30442288	PCS		19/39			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0000006	PMID:30442288	PCS					I	HPO:probinson[2021-07-08];HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0001645	PMID:30442288	PCS		11/68			P	HPO:probinson[2021-07-08]
OMIM:619402	Cardiomyopathy, familial hypertrophic, 28		HP:0032092	PMID:30442288	PCS		9/42			P	HPO:probinson[2021-07-08]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0003236	PMID:14506070	PCS		8/11			P	HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0000640	PMID:14506070	PCS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001332	OMIM:208920	TAS		5/14			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0003693	PMID:14506070	PCS		14/14			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001272	OMIM:208920	PCS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0002066	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001251	PMID:14506070	PCS		14/14			P	HPO:probinson[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0003073	PMID:14506070	PCS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0033051	PMID:14506070	PCS		8/11			P	HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0100543	PMID:14506070	PCS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0011463	PMID:14506070	PCS		6/13			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0040078	OMIM:208920	IEA					P	HPO:skoehler[2018-10-08]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0000657	PMID:14506070	PCS		12/14			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0002936	PMID:14506070	PCS		12/13			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001324	OMIM:208920	TAS					P	HPO:skoehler[2012-10-17]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001268	OMIM:208920	IEA		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001265	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0003621	PMID:14506070	PCS		9/13			C	HPO:probinson[2012-03-18];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0000571	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0002078	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0002650	PMID:14506070	PCS		6/12			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0003387	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001761	PMID:14506070	PCS		6/11			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0003124	PMID:14506070	PCS		9/12			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0000590	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001260	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0003581	OMIM:208920	TAS					C	HPO:skoehler[2012-10-17]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001284	PMID:14506070	PCS		12/13			P	HPO:iea[2012-04-24];HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0002072	PMID:14506070	PCS		11/14			P	HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0002070	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0000726	OMIM:208920	TAS					P	HPO:skoehler[2017-07-13]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0000007	OMIM:208920	TAS					I	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0002505	PMID:14506070	PCS	HP:0003581	11/14			P	HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0006886	PMID:14506070	PCS		11/11			P	HPO:probinson[2022-09-04]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0001337	OMIM:208920	TAS					P	HPO:iea[2012-04-24]
OMIM:208920	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia		HP:0000764	OMIM:208920	PCS					P	HPO:probinson[2012-03-18]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0000495	OMIM:217800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0003621	OMIM:217800	IEA					C	HPO:iea[2009-02-17]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0001131	OMIM:217800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0001939	OMIM:217800	IEA					P	HPO:iea[2009-02-17]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0000613	OMIM:217800	IEA					P	HPO:iea[2009-02-17]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0000007	OMIM:217800	IEA					I	HPO:iea[2009-02-17]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0007754	OMIM:217800	TAS					P	HPO:skoehler[2015-01-21]
OMIM:217800	Macular dystrophy, corneal, 1		HP:0007856	OMIM:217800	IEA					P	HPO:iea[2009-02-17]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0001397	PMID:20049731	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0003621	PMID:20049731	PCS		1/1			C	HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0002155	PMID:20049731	PCS	HP:0011462	1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0030796	PMID:20049731	PCS		1/1			P	HPO:probinson[2022-04-01];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0030685	PMID:20049731	PCS		1/1			P	HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0002240	PMID:20049731	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0003292	PMID:20049731	PCS		1/1			P	HPO:probinson[2022-04-01];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0000858	PMID:20049731	PCS		1/1			P	HPO:probinson[2022-04-01];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0000822	PMID:20049731	PCS		1/1			P	HPO:probinson[2022-04-01];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0000007	PMID:20049731	PCS					I	HPO:skoehler[2013-06-04];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0009125	PMID:20049731	PCS		1/1			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0000956	PMID:20049731	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-04-01]
OMIM:615238	Lipodystrophy, familial partial, type 5		HP:0001953	PMID:20049731	PCS		1/1			P	HPO:probinson[2022-04-01];HPO:probinson[2022-04-01]
OMIM:614640	UV-sensitive syndrome 3		HP:0003224	OMIM:614640	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614640	UV-sensitive syndrome 3		HP:0000992	OMIM:614640	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614640	UV-sensitive syndrome 3		HP:0000958	OMIM:614640	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614640	UV-sensitive syndrome 3		HP:0001480	OMIM:614640	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614640	UV-sensitive syndrome 3		HP:0003593	OMIM:614640	TAS					C	HPO:skoehler[2012-10-17]
OMIM:614640	UV-sensitive syndrome 3		HP:0001009	OMIM:614640	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614640	UV-sensitive syndrome 3		HP:0000007	PMID:22466610	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-28]
OMIM:229050	Folate malabsorption, hereditary		HP:0002024	OMIM:229050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:229050	Folate malabsorption, hereditary		HP:0001250	OMIM:229050	IEA					P	HPO:iea[2009-02-17]
OMIM:229050	Folate malabsorption, hereditary		HP:0001252	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0001251	OMIM:229050	IEA					P	HPO:iea[2009-02-17]
OMIM:229050	Folate malabsorption, hereditary		HP:0003593	PMID:17129779	PCS		2/2			C	HPO:skoehler[2010-06-19];HPO:probinson[2022-12-03]
OMIM:229050	Folate malabsorption, hereditary		HP:0001290	OMIM:229050	TAS					P	HPO:skoehler[2017-07-13]
OMIM:229050	Folate malabsorption, hereditary		HP:6000258	PMID:11804211	PCS					P	HPO:probinson[2024-02-27]
OMIM:229050	Folate malabsorption, hereditary		HP:0001508	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0002719	PMID:17129779	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-03]
OMIM:229050	Folate malabsorption, hereditary		HP:0000737	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0008872	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0100507	PMID:17129779	PCS		2/2			P	HPO:probinson[2022-12-03]
OMIM:229050	Folate malabsorption, hereditary		HP:0001249	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0002135	OMIM:229050	IEA					P	HPO:iea[2009-02-17]
OMIM:229050	Folate malabsorption, hereditary		HP:0002014	PMID:17129779	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:229050	Folate malabsorption, hereditary		HP:0004851	PMID:17129779	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:229050	Folate malabsorption, hereditary		HP:0001882	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0000155	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0001263	OMIM:229050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:229050	Folate malabsorption, hereditary		HP:0100660	OMIM:229050	TAS					P	HPO:skoehler[2013-05-31]
OMIM:229050	Folate malabsorption, hereditary		HP:0009830	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0000007	PMID:17129779	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-03]
OMIM:229050	Folate malabsorption, hereditary		HP:0002305	OMIM:229050	IEA					P	HPO:iea[2009-02-17]
OMIM:229050	Folate malabsorption, hereditary		HP:0001873	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:229050	Folate malabsorption, hereditary		HP:0001875	OMIM:229050	IEA					P	HPO:skoehler[2010-06-18]
OMIM:165590	Orofaciodigital syndrome X		HP:0001177	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0000175	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0000506	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0002990	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0000278	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0005280	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0005802	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0000006	OMIM:165590	IEA					I	HPO:iea[2009-02-17]
OMIM:165590	Orofaciodigital syndrome X		HP:0009380	OMIM:165590	IEA					P	HPO:iea[2009-02-17]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0002169	PMID:22717650	PCS		6/9			P	HPO:skoehler[2012-11-16];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0000750	PMID:22717650	PCS		6/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0001288	PMID:22717650	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0001332	PMID:22717650	PCS		2/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0001382	PMID:22717650	PCS		8/8			P	HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0002495	PMID:22717650	PCS		2/9			P	HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0001263	PMID:22717650	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0003593	PMID:22717650	PCS		6/9			C	HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0200049	PMID:22717650	PCS		6/9			P	HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0100543	PMID:22717650	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0002808	PMID:22717650	PCS		9/9			P	HPO:skoehler[2012-11-16];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0011463	PMID:22717650	PCS		3/9			C	HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0000998	PMID:22717650	PCS		3/9			P	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0000007	PMID:22717650	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0000768	PMID:22717650	PCS		7/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0006895	PMID:22717650	PCS		9/9			P	HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0001258	PMID:22717650	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-12-10]
OMIM:614898	Spastic paraplegia 53, autosomal recessive		HP:0001347	PMID:22717650	PCS		9/9			P	HPO:skoehler[2012-11-16];HPO:probinson[2020-12-10]
OMIM:617349	Aortic aneurysm, familial thoracic 11, susceptibility to		HP:0003581	PMID:26854927	PCS					C	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:617349	Aortic aneurysm, familial thoracic 11, susceptibility to		HP:0003829	PMID:26854927	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-02]
OMIM:617349	Aortic aneurysm, familial thoracic 11, susceptibility to		HP:0012499	PMID:26854927	PCS		1/10			P	HPO:probinson[2021-05-02];HPO:probinson[2021-05-02]
OMIM:617349	Aortic aneurysm, familial thoracic 11, susceptibility to		HP:0004933	PMID:26854927	PCS		7/10			P	HPO:probinson[2021-05-02]
OMIM:617349	Aortic aneurysm, familial thoracic 11, susceptibility to		HP:0000006	PMID:26854927	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-02]
OMIM:617349	Aortic aneurysm, familial thoracic 11, susceptibility to		HP:0004942	PMID:26854927	PCS					P	HPO:probinson[2021-05-02]
OMIM:148370	Keratolytic winter erythema		HP:0007410	OMIM:148370	IEA					P	HPO:skoehler[2019-02-22]
OMIM:148370	Keratolytic winter erythema		HP:0010783	OMIM:148370	IEA					P	HPO:skoehler[2015-01-27]
OMIM:148370	Keratolytic winter erythema		HP:0000006	OMIM:148370	IEA					I	HPO:iea[2009-02-17]
OMIM:148370	Keratolytic winter erythema		HP:0000951	OMIM:148370	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0001056	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000164	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0001770	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000486	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0002100	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0004322	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000161	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000480	OMIM:258865	IEA					P	HPO:skoehler[2018-10-08]
OMIM:258865	Orofaciodigital syndrome IX		HP:0010566	OMIM:258865	IEA					P	HPO:skoehler[2010-06-20]
OMIM:258865	Orofaciodigital syndrome IX		HP:0012444	OMIM:258865	IEA					P	HPO:skoehler[2018-10-08]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000316	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000218	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000455	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000456	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0005349	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000175	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000252	OMIM:258865	IEA					P	HPO:skoehler[2019-04-18]
OMIM:258865	Orofaciodigital syndrome IX		HP:0001161	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0001263	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000191	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0012385	OMIM:258865	IEA					P	HPO:skoehler[2018-10-08]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000506	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0001419	OMIM:258865	IEA					I	HPO:iea[2009-02-17]
OMIM:258865	Orofaciodigital syndrome IX		HP:0000007	OMIM:258865	IEA					I	HPO:skoehler[2019-04-18]
OMIM:258865	Orofaciodigital syndrome IX		HP:0005736	OMIM:258865	IEA					P	HPO:iea[2009-02-17]
OMIM:187501	Tetralogy of Fallot and glaucoma		HP:0001087	OMIM:187501	IEA					P	HPO:iea[2009-02-17]
OMIM:187501	Tetralogy of Fallot and glaucoma		HP:0001636	OMIM:187501	IEA					P	HPO:iea[2009-02-17]
OMIM:187501	Tetralogy of Fallot and glaucoma		HP:0000006	OMIM:187501	IEA					I	HPO:iea[2009-02-17]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001298	PMID:19375058	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001276	PMID:19375058	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0002059	PMID:19375058	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0002045	PMID:19375058	PCS	HP:0003623	1/1			P	HPO:probinson[2023-02-08]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001662	OMIM:614654	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001332	PMID:19375058	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001272	PMID:19375058	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0011968	PMID:19375058	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001250	PMID:19375058	PCS		1/1		HP:0031375	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001263	PMID:19375058	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001252	OMIM:614654	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0002151	OMIM:614654	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0005484	OMIM:614654	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001290	OMIM:614654	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0002093	OMIM:614654	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0034369	PMID:19375058	PCS		1/1			P	HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0000007	PMID:19375058	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001712	PMID:19375058	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001511	OMIM:614654	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001612	OMIM:614654	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0003348	OMIM:614654	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0001347	OMIM:614654	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0003128	PMID:19375058	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-07]
OMIM:614654	Coenzyme Q10 deficiency, primary, 5		HP:0003623	PMID:19375058	PCS		1/1			C	HPO:probinson[2023-02-07]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0000771	OMIM:201910	TAS	HP:0003581				P	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:6000516	PMID:34780778	PCS					P	HPO:probinson[2024-04-03]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0001507	OMIM:201910	IEA					P	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0008221	OMIM:201910	IEA					P	HPO:skoehler[2015-01-19]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0000822	OMIM:201910	IEA					P	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0000007	OMIM:201910	IEA					I	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0001943	OMIM:201910	IEA					P	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0001954	OMIM:201910	IEA					P	HPO:skoehler[2019-04-18]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0001945	OMIM:201910	IEA					P	HPO:skoehler[2010-06-20]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0000840	OMIM:201910	IEA					P	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0000047	OMIM:201910	IEA					P	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0000127	OMIM:201910	IEA					P	HPO:iea[2009-02-17]
OMIM:201910	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency		HP:0000765	OMIM:201910	IEA					P	HPO:iea[2009-02-17]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0002919	PMID:36595822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0001959	PMID:36595822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0011462	PMID:36595822	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0003074	PMID:36595822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0004904	PMID:17426099;PMID:36595822	PCS		11/11			P	HPO:probinson[2013-04-04];ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0032368	PMID:36595822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0040217	PMID:36595822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0000103	PMID:36595822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0040216	PMID:36595822	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0000006	PMID:17426099	PCS					I	HPO:probinson[2013-01-09]
OMIM:612225	Maturity-onset diabetes of the young, type IX		HP:0025329	PMID:36595822	PCS		0/1			P	ORCID:0000-0002-0736-9199[2024-07-14]
OMIM:613885	Meckel syndrome, type 8		HP:0000175	PMID:21462283	PCS		1/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000252	PMID:21462283	PCS		1/5			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0003577	PMID:21462283	PCS		5/5			C	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0001762	PMID:21462283	PCS		1/5			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000062	PMID:21462283	PCS		1/5			P	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0002085	PMID:21462283	PCS		3/5			P	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0003196	PMID:21462283	PCS		1/5			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000470	PMID:21462283	PCS		1/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0002084	PMID:21462283	PCS		5/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0003270	PMID:21462283	PCS		2/5			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0010442	PMID:21462283	PCS		5/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000528	PMID:21462283	PCS		1/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0004719	PMID:21462283	PCS		1/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000007	PMID:21462283	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000337	PMID:21462283	PCS		1/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000568	PMID:21462283	PCS		1/5			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0025700	PMID:21462283	PCS		1/5			P	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000774	PMID:21462283	PCS		1/5			P	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0001698	PMID:21462283	PCS		1/5			P	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000113	PMID:21462283	PCS		2/5			P	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000204	PMID:21462283	PCS		1/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000457	PMID:21462283	PCS		1/5			P	HPO:skoehler[2015-04-26];HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000105	PMID:21462283	PCS		1/5			P	HPO:probinson[2022-10-30]
OMIM:613885	Meckel syndrome, type 8		HP:0000369	PMID:21462283	PCS		1/5			P	HPO:probinson[2013-08-10];HPO:probinson[2022-10-30]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0001320	PMID:22983954	PCS		1/2			P	HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000340	PMID:22983954	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0003577	PMID:22983954	PCS		4/4			C	HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000574	PMID:22983954	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000750	PMID:22983954	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0004322	PMID:22983954	PCS		4/4			P	HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0001250	PMID:22983954	PCS		0/4			P	HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0001263	PMID:22983954	PCS		4/4			P	HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0100710	OMIM:604321	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000718	OMIM:604321	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0011451	PMID:22983954	PCS		4/4			P	HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000316	OMIM:604321	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000007	PMID:22983954	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0009765	PMID:22983954	PCS		4/4			P	HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0001335	OMIM:604321	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000664	PMID:22983954	PCS		4/4			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0001249	PMID:22983954	PCS		4/4			P	HPO:skoehler[2013-06-16];HPO:probinson[2022-12-17]
OMIM:604321	Microcephaly 4, primary, autosomal recessive		HP:0000347	OMIM:604321	IEA					P	HPO:skoehler[2018-10-08]
OMIM:607628	Epilepsy with grand mal seizures on awakening		HP:0007193	OMIM:607628	TAS					P	HPO:probinson[2009-02-17]
OMIM:607628	Epilepsy with grand mal seizures on awakening		HP:0002123	OMIM:607628	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:607628	Epilepsy with grand mal seizures on awakening		HP:0002121	OMIM:607628	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:607628	Epilepsy with grand mal seizures on awakening		HP:0000006	OMIM:607628	TAS					I	HPO:probinson[2009-02-17]
OMIM:131880	Epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase		HP:0008066	OMIM:131880	TAS					P	HPO:probinson[2013-12-16]
OMIM:131880	Epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase		HP:0003593	OMIM:131880	TAS					C	HPO:probinson[2009-02-17]
OMIM:131880	Epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase		HP:0000006	OMIM:131880	TAS					I	HPO:probinson[2009-02-17]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0010739	PMID:28434888	PCS		1/1			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-20]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0010816	PMID:28434888	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0003764	PMID:28434888	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-20]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0003577	PMID:28434888	PCS		1/1			C	HPO:probinson[2023-02-20]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0002650	PMID:28434888	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0001387	OMIM:166700	IEA					P	HPO:iea[2009-02-17]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0001371	OMIM:166700	IEA					P	HPO:skoehler[2010-06-20]
OMIM:166700	Buschke-Ollendorff syndrome		HP:6000943	PMID:30430046	PCS					P	HPO:probinson[2024-08-03]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0100898	OMIM:166700	IEA					P	HPO:skoehler[2018-10-08]
OMIM:166700	Buschke-Ollendorff syndrome		HP:6000817	OMIM:166700	TAS					P	HPO:probinson[2024-08-03]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0001609	OMIM:166700	IEA					P	HPO:iea[2009-02-17]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0100559	PMID:28434888	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:166700	Buschke-Ollendorff syndrome		HP:0000006	PMID:15489854	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001298	PMID:20206331	PCS		1/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0006824	OMIM:211530	TAS					P	HPO:skoehler[2015-01-04]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0010628	PMID:20206331	PCS		2/9			P	HPO:skoehler[2015-01-04]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0003676	PMID:20206331	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0000365	PMID:20206331	PCS		2/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0010307	PMID:20206331	PCS		3/9			P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001252	PMID:20206331	PCS		2/9			P	HPO:skoehler[2010-06-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001251	OMIM:211530	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002141	PMID:20206331	PCS		1/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0003593	PMID:20206331	PCS		3/9			C	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0012473	PMID:20206331	PCS		1/9			P	HPO:skoehler[2013-11-28]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0011463	PMID:20206331	PCS		2/9			C	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001308	PMID:20206331	PCS		2/9			P	HPO:iea[2009-02-17]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001605	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001324	PMID:20206331	PCS		3/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0003701	PMID:20206331	PCS		1/9			P	HPO:skoehler[2010-06-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001621	OMIM:211530	IEA					P	HPO:skoehler[2010-06-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002877	OMIM:211530	IEA					P	HPO:iea[2009-02-17]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001348	PMID:20206331	PCS		1/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001347	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002058	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0003202	PMID:20206331	PCS		2/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002312	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002015	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0003324	PMID:20206331	PCS		1/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0003621	PMID:20206331	PCS		4/9			C	HPO:iea[2009-02-17]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002650	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002078	PMID:20206331	PCS		1/9			P	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001283	PMID:20206331	PCS		3/9			P	HPO:iea[2009-02-17]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002098	PMID:20206331	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002094	OMIM:211530	TAS					P	HPO:skoehler[2013-11-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002093	PMID:20206331	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0011449	OMIM:211530	IEA					P	HPO:skoehler[2010-06-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0011448	PMID:20206331	PCS		1/9			P	HPO:skoehler[2012-10-17]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0009130	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0007097	OMIM:211530	IEA					P	HPO:iea[2009-02-17]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0003819	PMID:20206331	PCS		1/9			C	HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002808	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0000407	PMID:20206331	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0009113	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0000508	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0001317	OMIM:211530	IEA					P	HPO:skoehler[2018-10-08]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0009830	PMID:20206331	PCS		1/9			P	HPO:skoehler[2010-06-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0000007	PMID:20206331	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-04-11]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0002205	OMIM:211530	IEA					P	HPO:skoehler[2010-06-20]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0000544	PMID:20206331	PCS		1/9			P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0000467	OMIM:211530	IEA					P	HPO:skoehler[2010-06-18]
OMIM:211530	Brown-Vialetto-Van Laere syndrome 1		HP:0004887	PMID:20206331	PCS		1/9			P	HPO:probinson[2023-04-11]
OMIM:162200	Neurofibromatosis, type 1		HP:0004322	PMID:11106357	PCS		50/385			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:162200	Neurofibromatosis, type 1		HP:0001250	PMID:29566708	PCS		19/437			P	HPO:probinson[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:6001124	OMIM:162200	TAS					P	HPO:probinson[2024-12-14]
OMIM:162200	Neurofibromatosis, type 1		HP:0003593	PMID:20301288	PCS					C	HPO:probinson[2022-04-03]
OMIM:162200	Neurofibromatosis, type 1		HP:0011463	PMID:20301288	PCS					C	HPO:probinson[2022-04-03]
OMIM:162200	Neurofibromatosis, type 1		HP:0012032	PMID:7607663;PMID:26178382;PMID:36659944;PMID:9101303;PMID:8664912;PMID:29290338;PMID:17160901	PCS		9/328			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000316	PMID:38596211	PCS		3/15			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002858	OMIM:162200	IEA					P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001328	PMID:10204844	PCS		186/300			P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000997	PMID:7607663;PMID:26178382;PMID:36659944;PMID:38596211;PMID:9101303;PMID:8664912;PMID:10204844;PMID:29290338	PCS		435/546			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000238	OMIM:162200	IEA					P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002859	OMIM:162200	IEA					P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0007565	PMID:7607663;PMID:20513137;PMID:26178382;PMID:36659944;PMID:38596211;PMID:9101303;PMID:8664912;PMID:10204844;PMID:29290338	PCS		677/781			P	HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002857	OMIM:162200	IEA					P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002414	OMIM:162200	IEA		151/357			P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001642	PMID:26178382;PMID:29290338;PMID:17160901	PCS		18/267			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001920	PMID:10204844;PMID:29290338	PCS		4/641			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002897	OMIM:162200	IEA					P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001067	PMID:7607663;PMID:20513137;PMID:26178382;PMID:38596211;PMID:9101303;PMID:8664912;PMID:10204844;PMID:29290338	PCS		297/457			P	HPO:iea[2018-03-13];ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000494	PMID:38596211	PCS		4/15			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0007429	PMID:20513137;PMID:26178382;PMID:38596211;PMID:29290338	PCS		48/56			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0003002	PMID:7607663;PMID:36659944;PMID:9101303;PMID:8664912;PMID:29290338	PCS		1/148			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0003003	PMID:7607663;PMID:36659944;PMID:9101303;PMID:8664912;PMID:29290338	PCS		1/148			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0010795	PMID:7607663;PMID:38596211;PMID:36659944;PMID:9101303;PMID:8664912;PMID:29290338	PCS		2/163			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0100697	OMIM:162200	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2019-01-22]
OMIM:162200	Neurofibromatosis, type 1		HP:0000767	PMID:7607663;PMID:26178382;PMID:36659944;PMID:38596211;PMID:9101303;PMID:8664912;PMID:29618358;PMID:29290338;PMID:17160901	PCS		24/439			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:probinson[2019-01-22]
OMIM:162200	Neurofibromatosis, type 1		HP:0009733	PMID:26178382;PMID:38596211	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000768	PMID:26178382;PMID:38596211;PMID:29290338	PCS		13/274			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0009732	PMID:7607663;PMID:20513137;PMID:23035791;PMID:26178382;PMID:36659944;PMID:38596211;PMID:9101303;PMID:8664912;PMID:29290338;PMID:17160901	PCS		139/554			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002865	PMID:7607663;PMID:36659944;PMID:9101303;PMID:8664912;PMID:29290338	PCS		1/148			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0009735	PMID:10204844;PMID:29290338	PCS		34/354			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0006743	PMID:7607663;PMID:36659944;PMID:9101303;PMID:8664912;PMID:29290338	PCS		3/148			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0009734	PMID:20513137;PMID:26178382;PMID:38596211;PMID:8664912;PMID:10204844;PMID:29290338	PCS		64/476			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000006	PMID:10204844	PCS					I	HPO:probinson[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0009737	PMID:7607663;PMID:20513137;PMID:26178382;PMID:38596211;PMID:36659944;PMID:8664912;PMID:10204844;PMID:29290338;PMID:17160901	PCS		240/533			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000369	PMID:38596211	PCS		2/15			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002666	PMID:25130111	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0009736	PMID:10204844	PCS		10/300			P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002521	PMID:18802710	PCS					P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0020073	PMID:17105749	PCS					P	HPO:probinson[2019-04-20]
OMIM:162200	Neurofibromatosis, type 1		HP:0001629	PMID:26178382;PMID:29290338	PCS		2/223			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001548	OMIM:162200	IEA					P	HPO:skoehler[2010-06-20]
OMIM:162200	Neurofibromatosis, type 1		HP:0001701	PMID:29290338	PCS		1/118			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000256	PMID:31326214	PCS		48/128			P	HPO:iea[2009-02-17];HPO:probinson[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002410	OMIM:162200	IEA					P	HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002650	PMID:7607663;PMID:20513137;PMID:26178382;PMID:36659944;PMID:38596211;PMID:9101303;PMID:8664912;PMID:29290338;PMID:17160901	PCS		56/365			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17];HPO:probinson[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001480	PMID:20513137;PMID:26178382;PMID:29290338;PMID:17160901	PCS		146/224			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001680	PMID:29290338	PCS		1/118			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0033680	PMID:7607663;PMID:36659944;PMID:9101303;PMID:8664912;PMID:29290338	PCS		1/148			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0009592	PMID:26178382;PMID:29290338	PCS		2/137			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:skoehler[2010-06-20];HPO:probinson[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001639	PMID:29290338	PCS		1/118			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0002808	PMID:7607663;PMID:26178382;PMID:38596211;PMID:36659944;PMID:9101303;PMID:8664912	PCS		2/145			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001718	PMID:29290338	PCS		1/118			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000822	OMIM:162200;PMID:26178382;PMID:29290338	PCS		10/238			P	ORCID:0000-0002-0736-9199[2024-08-17];HPO:iea[2009-02-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0030052	PMID:10204844	PCS	HP:0011463	151/357			P	HPO:skoehler[2014-09-21]
OMIM:162200	Neurofibromatosis, type 1		HP:0030052	PMID:38596211	PCS		11/15			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0030052	PMID:9101303	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0030052	PMID:26178382	PCS		8/22			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0030052	PMID:36659944	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0030052	PMID:8664912	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0030052	PMID:29290338	PCS		69/130			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0001631	PMID:26178382;PMID:29290338;PMID:17160901	PCS		3/267			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000465	PMID:38596211	PCS		1/15			P	ORCID:0000-0002-0736-9199[2024-08-17]
OMIM:162200	Neurofibromatosis, type 1		HP:0000501	PMID:22138687	PCS					P	HPO:iea[2009-02-17]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001410	OMIM:614867	TAS					P	HPO:probinson[2013-02-24]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001310	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001272	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0003593	PMID:10528859	PCS		1/1			C	HPO:probinson[2022-10-20]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001251	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001290	OMIM:614867	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000639	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0003828	OMIM:614867	TAS					M	HPO:skoehler[2015-12-30]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0010571	OMIM:614867	TAS					P	HPO:probinson[2013-02-24]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0009046	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000514	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000657	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0002317	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000510	PMID:10528859	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2022-10-20]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000556	OMIM:614867	TAS					P	HPO:probinson[2013-02-24]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001265	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001761	OMIM:614867	TAS		HP:0040283			P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001382	PMID:10528859	PCS		1/1			P	HPO:probinson[2022-10-20]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001260	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001263	PMID:10528859	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2022-10-20]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0003819	PMID:10528859	PCS		1/1			C	HPO:probinson[2022-10-20]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000407	OMIM:614867	TAS					P	HPO:probinson[2013-02-24]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0008167	PMID:10528859	PCS		1/1			P	HPO:probinson[2013-02-24];HPO:probinson[2022-10-20]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000007	PMID:10528859	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-10-20]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0000505	OMIM:614867	TAS					P	HPO:probinson[2013-02-24]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001319	OMIM:614867	TAS					P	HPO:probinson[2013-02-24]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0001337	OMIM:614867	TAS					P	HPO:skoehler[2015-02-22]
OMIM:614867	Peroxisome biogenesis disorder 5B		HP:0003677	OMIM:614867	TAS					C	HPO:skoehler[2015-12-30]
OMIM:301051	Immunodeficiency 74, COVID19-related, X-linked		HP:0033141	PMID:32706371	PCS		4/4			P	HPO:probinson[2020-10-12]
OMIM:301051	Immunodeficiency 74, COVID19-related, X-linked		HP:0001419	PMID:32706371	PCS					I	HPO:probinson[2020-09-13];HPO:probinson[2020-09-13]
OMIM:301051	Immunodeficiency 74, COVID19-related, X-linked		HP:0031691	PMID:32706371	PCS		4/4			P	HPO:probinson[2020-09-13]
OMIM:618091	Spermatogenic failure 29		HP:0003251	PMID:28554943	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:618091	Spermatogenic failure 29		HP:0011462	PMID:28554943	PCS		2/2			C	HPO:probinson[2023-02-18]
OMIM:618091	Spermatogenic failure 29		HP:0000007	PMID:28554943	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-18]
OMIM:618091	Spermatogenic failure 29		HP:0012208	PMID:28554943	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:618091	Spermatogenic failure 29		HP:0011961	PMID:28554943	PCS		2/2			P	HPO:probinson[2023-02-18]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0001397	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0004313	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0001410	PMID:29127204	PCS	HP:0003593	3/3			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0001541	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0002240	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0003593	PMID:29127204	PCS					C	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0012301	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0002719	PMID:29127204	PCS		3/3			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0001419	PMID:29127204	PCS					I	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0002910	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0000047	PMID:29127204	PCS		2/3			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0000952	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0000347	PMID:29127204	PCS		2/3			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0000369	PMID:29127204	PCS		2/3			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0000973	PMID:29127204	PCS		3/3			P	HPO:probinson[2020-07-24];HPO:probinson[2020-07-24]
OMIM:301045	Congenital disorder of glycosylation, type IIr		HP:0001413	PMID:29127204	PCS					P	HPO:probinson[2020-07-24]
OMIM:614873	Peroxisome biogenesis disorder 7B		HP:0001410	OMIM:614873	TAS					P	HPO:probinson[2013-02-24]
OMIM:614873	Peroxisome biogenesis disorder 7B		HP:0000407	OMIM:614873	TAS					P	HPO:probinson[2013-02-24]
OMIM:614873	Peroxisome biogenesis disorder 7B		HP:0001263	OMIM:614873	TAS					P	HPO:probinson[2013-02-24]
OMIM:614873	Peroxisome biogenesis disorder 7B		HP:0000007	OMIM:614873	TAS					I	HPO:probinson[2013-01-09]
OMIM:614873	Peroxisome biogenesis disorder 7B		HP:0000505	OMIM:614873	TAS					P	HPO:probinson[2013-02-24]
OMIM:614873	Peroxisome biogenesis disorder 7B		HP:0001319	OMIM:614873	TAS					P	HPO:probinson[2013-02-24]
OMIM:614873	Peroxisome biogenesis disorder 7B		HP:0000556	OMIM:614873	TAS					P	HPO:probinson[2013-02-24]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001254	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001250	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0003210	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001252	PMID:33029243	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0002240	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0003593	OMIM:251100	IEA					C	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001290	OMIM:251100	TAS					P	HPO:skoehler[2017-07-13]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0031962	PMID:33029243	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0002919	PMID:33029243	PCS		1/1			P	HPO:skoehler[2010-06-20]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001508	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0034661	PMID:33029243	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001903	OMIM:251100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0034662	PMID:33029243	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001944	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0008872	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001987	PMID:33029243	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001946	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0002912	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001348	PMID:33029243	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001942	PMID:33029243	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0003145	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0002013	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0002098	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0002154	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001263	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0040126	PMID:33029243	PCS		0/1			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-15]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0012120	PMID:33029243	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-15]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0000007	PMID:12438653	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-15]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001873	OMIM:251100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001876	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001337	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001259	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:251100	Methylmalonic aciduria, vitamin B12-responsive, cblA type		HP:0001875	OMIM:251100	IEA					P	HPO:iea[2009-02-17]
OMIM:174310	Polydactyly, postaxial, with progressive myopia		HP:0001162	OMIM:174310	IEA					P	HPO:iea[2009-02-17]
OMIM:174310	Polydactyly, postaxial, with progressive myopia		HP:0000006	OMIM:174310	IEA					I	HPO:iea[2009-02-17]
OMIM:174310	Polydactyly, postaxial, with progressive myopia		HP:0000545	OMIM:174310	IEA					P	HPO:iea[2009-02-17]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0002463	PMID:26010655	PCS					P	HPO:probinson[2017-06-23]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0000750	OMIM:616902	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0001250	PMID:26010655	PCS					P	HPO:probinson[2017-06-23]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0001263	PMID:26010655	PCS					P	HPO:probinson[2017-06-23]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0000717	PMID:26010655	PCS					P	HPO:probinson[2017-06-23]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0003829	OMIM:616902	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0000526	OMIM:616902	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0000006	PMID:26010655	PCS					I	HPO:probinson[2017-06-23]
OMIM:616902	Chromosome 11P13 deletion syndrome, distal		HP:0001249	OMIM:616902	TAS					P	HPO:skoehler[2017-07-13]
OMIM:139210	Myhre syndrome		HP:0001650	OMIM:139210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0000365	PMID:22158539;PMID:22243968;PMID:24715504	PCS		17/20			P	HPO:skoehler[2010-06-20];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001773	PMID:22158539	PCS		11/11			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000486	PMID:22158539	PCS		3/11			P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0001376	PMID:22158539	PCS		11/11			P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0004322	PMID:22158539	PCS		9/11			P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0001250	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0000160	PMID:22243968	PCS		7/8			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0001251	OMIM:139210	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:139210	Myhre syndrome		HP:0410030	PMID:22243968	PCS	HP:0003577	1/8			P	HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0009381	OMIM:139210	TAS					P	HPO:probinson[2012-06-10]
OMIM:139210	Myhre syndrome		HP:0000518	PMID:22243968	PCS		1/7			P	HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0011463	PMID:24715504	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001608	OMIM:139210	TAS					P	HPO:skoehler[2013-03-10]
OMIM:139210	Myhre syndrome		HP:0000717	PMID:22243968	PCS		2/8			P	HPO:skoehler[2010-06-20];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0002938	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000316	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0001845	OMIM:139210	TAS					P	HPO:skoehler[2012-11-21]
OMIM:139210	Myhre syndrome		HP:0009466	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0000752	PMID:22158539;PMID:24715504	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001643	PMID:22158539	PCS		5/11			P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0001642	PMID:22158539	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001249	OMIM:139210	TAS					P	HPO:skoehler[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0002553	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000175	PMID:22243968	PCS		1/8			P	HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0003720	PMID:22158539;PMID:24715504	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-05-11];HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0000252	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0000574	OMIM:139210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0002750	PMID:22158539	PCS		5/7			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001387	PMID:22243968;PMID:24715504	PCS		9/9			P	HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0004894	OMIM:139210	TAS					P	HPO:skoehler[2012-11-21]
OMIM:139210	Myhre syndrome		HP:0003561	PMID:22243968	PCS	HP:0003577	3/5			P	HP:probinson[2019-03-02];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000490	OMIM:139210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0001263	PMID:22158539;PMID:24715504	PCS		10/12			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0004691	OMIM:139210	TAS					P	HPO:skoehler[2012-11-21]
OMIM:139210	Myhre syndrome		HP:0011800	PMID:22243968	PCS		8/8			P	HPO:skoehler[2013-11-28];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0012385	OMIM:139210	TAS					P	HPO:skoehler[2013-10-22]
OMIM:139210	Myhre syndrome		HP:0002948	OMIM:139210	TAS					P	HPO:skoehler[2012-11-21]
OMIM:139210	Myhre syndrome		HP:0000926	PMID:22158539;PMID:22243968	PCS		10/17			P	ORCID:0000-0002-0736-9199[2024-05-11];HPO:probinson[2013-04-14];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000327	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0000568	OMIM:139210	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:139210	Myhre syndrome		HP:0000527	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0004209	PMID:22158539	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001698	OMIM:139210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0003712	PMID:22243968	PCS		8/8			P	HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0002866	PMID:22243968	PCS		8/8			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000960	PMID:22158539	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000322	PMID:22158539;PMID:22243968	PCS		19/19			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000006	PMID:22243968	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000369	OMIM:139210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0000885	PMID:22243968	PCS		4/8			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0001276	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000385	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000220	PMID:22158539	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0004621	PMID:22158539;PMID:24715504	PCS		10/10			P	ORCID:0000-0002-0736-9199[2024-05-11];HPO:probinson[2013-04-14]
OMIM:139210	Myhre syndrome		HP:0001156	PMID:24715504	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000540	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0002684	PMID:22158539;PMID:22243968;PMID:24715504	PCS		18/18			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000581	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0001072	PMID:22158539;OMIM:139210	PCS		19/21			P	ORCID:0000-0002-0736-9199[2024-05-11];HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0008070	OMIM:139210	TAS					P	HPO:skoehler[2012-11-26]
OMIM:139210	Myhre syndrome		HP:0001629	PMID:22243968	PCS		1/8			P	HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0009088	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0100867	PMID:22158539	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0008551	PMID:22158539	PCS		2/11			P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0002878	OMIM:139210	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:139210	Myhre syndrome		HP:0000219	PMID:22243968;OMIM:139210	PCS		17/18			P	HP:probinson[2019-03-02];HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0000256	PMID:22243968	PCS		2/8			P	HP:probinson[2019-03-02];HPO:probinson[2019-07-03]
OMIM:139210	Myhre syndrome		HP:0003026	PMID:22158539	PCS		9/9			P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0002213	OMIM:139210	TAS	HP:0003577				P	HPO:skoehler[2012-11-21]
OMIM:139210	Myhre syndrome		HP:0004279	PMID:22158539;PMID:24715504	PCS		12/12			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001680	OMIM:139210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0000272	OMIM:139210	TAS					P	HPO:skoehler[2012-10-17]
OMIM:139210	Myhre syndrome		HP:0000470	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0045025	PMID:22158539;PMID:22243968	PCS		18/19			P	HPO:skoehler[2018-10-08];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0002093	OMIM:139210	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:139210	Myhre syndrome		HP:0010579	PMID:22158539	PCS		5/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0000709	PMID:22158539;PMID:24715504	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0032152	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0002808	PMID:24715504	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001518	PMID:22243968	PCS	HP:0003577	5/7			P	HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000822	PMID:22243968	PCS		2/8			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000426	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0030053	PMID:22243968	PCS		6/8			P	HPO:skoehler[2014-09-21];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0001511	OMIM:139210	IEA					P	HPO:iea[2009-02-17]
OMIM:139210	Myhre syndrome		HP:0001631	PMID:22243968	PCS		1/8			P	HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000028	PMID:22243968	PCS		2/5	MALE		P	HPO:iea[2009-02-17];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0000303	PMID:22158539;PMID:22243968;PMID:24715504	PCS		20/20			P	HPO:iea[2009-02-17];HP:probinson[2019-03-02];ORCID:0000-0002-0736-9199[2024-05-11]
OMIM:139210	Myhre syndrome		HP:0001513	PMID:22243968	PCS		5/8			P	HPO:skoehler[2012-11-18];HP:probinson[2019-03-02]
OMIM:139210	Myhre syndrome		HP:0001831	OMIM:139210	TAS					P	HPO:probinson[2012-06-10]
OMIM:137215	Gastric cancer, hereditary diffuse		HP:0000175	OMIM:137215	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:137215	Gastric cancer, hereditary diffuse		HP:0002582	OMIM:137215	IEA					P	HPO:iea[2009-02-17]
OMIM:137215	Gastric cancer, hereditary diffuse		HP:0003581	PMID:11443625	PCS		5/5			C	HPO:probinson[2022-04-24]
OMIM:137215	Gastric cancer, hereditary diffuse		HP:0012126	PMID:11443625	PCS		5/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2022-04-24]
OMIM:137215	Gastric cancer, hereditary diffuse		HP:0000006	PMID:9537325	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-04-24]
OMIM:137215	Gastric cancer, hereditary diffuse		HP:0000204	OMIM:137215	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:618907	Silver-Russell syndrome 4		HP:0004325	PMID:28796236	PCS		3/4			P	HPO:probinson[2020-08-12]
OMIM:618907	Silver-Russell syndrome 4		HP:0003561	PMID:28796236	PCS	HP:0003577	5/5			P	HPO:probinson[2020-08-12]
OMIM:618907	Silver-Russell syndrome 4		HP:0001518	PMID:28796236	PCS	HP:0003577	4/5			P	HPO:probinson[2020-08-12]
OMIM:618907	Silver-Russell syndrome 4		HP:0011220	PMID:28796236	PCS		4/5			P	HPO:probinson[2020-08-12]
OMIM:618907	Silver-Russell syndrome 4		HP:0008872	PMID:28796236	PCS	HP:0003593	4/4			P	HPO:probinson[2020-08-12]
OMIM:618907	Silver-Russell syndrome 4		HP:0040196	PMID:28796236	PCS		3/5			P	HPO:probinson[2020-08-12]
OMIM:618907	Silver-Russell syndrome 4		HP:0000006	PMID:28796236	PCS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618907	Silver-Russell syndrome 4		HP:0000325	PMID:28796236	PCS		5/5			P	HPO:probinson[2020-08-12]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000341	PMID:34424553	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0002521	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0010804	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0003236	PMID:30237576	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0002169	PMID:30237576	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000486	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0002188	PMID:30237576;PMID:26742501	PCS		2/2			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0001371	PMID:30237576	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0002120	PMID:34424553	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0001252	PMID:30237576;PMID:26742501;PMID:34424553	PCS		3/3			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0003593	PMID:26742501;PMID:34424553	PCS		2/2			C	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0100295	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0012444	PMID:30237576	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0033725	PMID:30237576;PMID:26742501;PMID:34424553	PCS		3/3			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0012469	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0001508	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000319	PMID:34424553	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0011220	PMID:34424553	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000253	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000252	PMID:30237576;PMID:34424553	PCS		2/2			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000750	PMID:30237576	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0001263	PMID:30237576;PMID:26742501;PMID:34424553	PCS		3/3			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0005280	PMID:34424553	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000007	PMID:26742501	PCS					I	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0007359	PMID:34424553	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000347	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:620240	Developmental delay with hypotonia, myopathy, and brain abnormalities		HP:0000248	PMID:26742501	PCS		1/1			P	HPO:probinson[2023-06-16]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000286	OMIM:300373	TAS					P	HPO:probinson[2009-02-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002025	OMIM:300373	IEA		HP:0040284			P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0003038	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002023	OMIM:300373	IEA		HP:0040284			P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0004322	OMIM:300373	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001250	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001252	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002020	OMIM:300373	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001290	OMIM:300373	IEA					P	HPO:skoehler[2017-07-13]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000316	OMIM:300373	TAS					P	HPO:probinson[2009-02-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000239	OMIM:300373	TAS					P	HPO:probinson[2009-02-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000678	OMIM:300373	TAS					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000238	OMIM:300373	TAS					P	HPO:probinson[2009-02-17]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002779	OMIM:300373	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001643	OMIM:300373	IEA					P	HPO:skoehler[2009-02-22]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000358	OMIM:300373	TAS					P	HPO:probinson[2009-02-19]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000175	OMIM:300373	TAS					P	HPO:probinson[2009-02-17]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000695	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0005464	OMIM:300373	TAS					P	HPO:skoehler[2014-05-04]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002990	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0012385	OMIM:300373	TAS					P	HPO:skoehler[2015-05-04]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000767	OMIM:300373	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000689	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001338	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0005619	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0006784	OMIM:300373	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001539	OMIM:300373	IEA		HP:0040284			P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0004209	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000405	OMIM:300373	TAS					P	HPO:probinson[2009-02-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0006587	OMIM:300373	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000201	OMIM:300373	IEA					P	HPO:skoehler[2009-02-17]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000003	OMIM:300373	IEA		HP:0040284			P	HPO:skoehler[2009-02-17]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002104	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000204	OMIM:300373	TAS					P	HPO:probinson[2009-02-17]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000369	OMIM:300373	TAS					P	HPO:probinson[2009-02-19]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000885	OMIM:300373	TAS					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001611	OMIM:300373	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000341	OMIM:300373	TAS					P	HPO:probinson[2009-02-19]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0010628	OMIM:300373	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0005830	OMIM:300373	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001476	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0005950	OMIM:300373	IEA					P	HPO:skoehler[2014-06-24]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002684	OMIM:300373	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0003298	OMIM:300373	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0010740	OMIM:300373	TAS					P	HPO:skoehler[2015-11-24]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001508	OMIM:300373	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001629	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0008551	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000218	OMIM:300373	TAS		15%			P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0006610	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001423	PMID:22043478	PCS					I	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002315	OMIM:300373	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000256	OMIM:300373	TAS					P	HPO:probinson[2009-02-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000179	OMIM:300373	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001166	OMIM:300373	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001562	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000396	OMIM:300373	TAS					P	HPO:probinson[2009-02-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001561	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002694	OMIM:300373	TAS					P	HPO:probinson[2015-03-22]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001762	OMIM:300373	IEA					P	HPO:skoehler[2009-02-22]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000431	OMIM:300373	IEA					P	HPO:skoehler[2009-02-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002650	OMIM:300373	TAS		23%			P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000750	OMIM:300373	IEA		10%			P	HPO:skoehler[2010-06-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000193	OMIM:300373	TAS					P	HPO:probinson[2009-02-17]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0009473	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002007	OMIM:300373	TAS					P	HPO:probinson[2009-02-23]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0001631	OMIM:300373	TAS					P	HPO:probinson[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000465	OMIM:300373	TAS					P	HPO:probinson[2009-02-20]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0002566	OMIM:300373	IEA					P	HPO:skoehler[2009-02-21]
OMIM:300373	Osteopathia striata with cranial sclerosis		HP:0000347	OMIM:300373	TAS					P	HPO:probinson[2009-02-19]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0001265	PMID:24925318	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0003236	PMID:24925318	PCS		3/3			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0031936	PMID:24925318	PCS		2/2			P	HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0003551	PMID:24925318	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0003593	PMID:24925318	PCS		2/2			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0003560	PMID:24925318	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0001270	PMID:24925318	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0003391	PMID:24925318	PCS		1/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0002280	PMID:24925318	PCS		1/2			P	HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0000007	PMID:24925318	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0001319	PMID:24925318	PCS		2/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-13]
OMIM:616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12		HP:0003325	PMID:24925318	PCS		2/2			P	HPO:probinson[2022-12-13];HPO:probinson[2022-12-13]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001374	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000486	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0004322	PMID:18478038	PCS		3/3			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001250	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000160	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001252	PMID:11092761;PMID:18478038	PCS		6/6			P	HPO:probinson[2023-02-10];HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0003593	PMID:11092761;PMID:18478038	PCS		6/6			C	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0500163	PMID:11092761;PMID:18478038	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000518	PMID:11092761;PMID:18478038	PCS		3/6			P	HPO:probinson[2023-02-10];HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0011220	OMIM:219150	TAS					P	HPO:skoehler[2012-10-17]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000316	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000239	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0003745	OMIM:219150	IEA					I	HPO:skoehler[2010-06-19]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001249	OMIM:219150	IEA					P	HPO:iea[2009-02-17]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001344	PMID:18478038	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002750	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001382	PMID:11092761	PCS		2/2			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002395	PMID:18478038	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001263	PMID:11092761;PMID:18478038	PCS		6/6			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001181	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0007394	PMID:18478038	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002827	PMID:18478038	PCS		3/4			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000767	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001537	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000007	PMID:11092761	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000601	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000400	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002305	PMID:18478038	PCS		2/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000248	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000369	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000963	OMIM:219150	IEA					P	HPO:skoehler[2010-06-20]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000023	OMIM:219150	IEA					P	HPO:iea[2009-02-17]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0003693	PMID:18478038	PCS		4/4			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0003572	PMID:11092761	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0008070	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001508	PMID:11092761;PMID:18478038	PCS		6/6			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-10];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000418	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001987	PMID:11092761;PMID:18478038	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000974	PMID:11092761	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000973	PMID:18478038	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001347	PMID:18478038	PCS		4/4			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002650	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001762	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0005961	PMID:11092761;PMID:18478038	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001084	OMIM:219150	IEA					P	HPO:iea[2009-02-17]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002572	PMID:11092761	PCS		2/2			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0010537	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0500139	PMID:11092761;PMID:18478038	PCS		2/6			P	HPO:probinson[2023-02-10]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002007	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0001511	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0002645	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000028	OMIM:219150	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:219150	Cutis laxa, autosomal recessive, type IIIA		HP:0000545	OMIM:219150	IEA					P	HPO:skoehler[2010-06-18]
OMIM:615589	Otosclerosis 10		HP:0000362	OMIM:615589	IEA					P	HPO:skoehler[2015-01-27]
OMIM:615589	Otosclerosis 10		HP:0000006	OMIM:615589	TAS					I	HPO:skoehler[2014-02-06]
OMIM:133701	Exostoses, multiple, type II		HP:0002762	PMID:8782816;PMID:11432960	PCS		17/17			P	HPO:probinson[2022-03-31]
OMIM:133701	Exostoses, multiple, type II		HP:0003621	PMID:11432960	PCS		3/9			C	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:133701	Exostoses, multiple, type II		HP:0003068	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0004322	OMIM:133701	IEA		0/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:133701	Exostoses, multiple, type II		HP:0003276	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0003593	PMID:11432960	IEA		1/9			C	HPO:probinson[2022-03-31]
OMIM:133701	Exostoses, multiple, type II		HP:0010049	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0000918	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0011463	PMID:11432960	PCS		5/9			C	HPO:probinson[2022-03-31]
OMIM:133701	Exostoses, multiple, type II		HP:0002812	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0003406	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0002318	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0002857	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0006765	PMID:8782816;PMID:11432960	PCS		1/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31];HPO:probinson[2022-03-31]
OMIM:133701	Exostoses, multiple, type II		HP:0000006	PMID:8782816	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:133701	Exostoses, multiple, type II		HP:0003105	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:133701	Exostoses, multiple, type II		HP:0000896	OMIM:133701	IEA					P	HPO:iea[2009-02-17]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0002378	OMIM:604484	TAS		HP:0040283			P	HPO:skoehler[2013-09-30]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0002398	OMIM:604484	TAS					P	HPO:probinson[2012-04-11]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0001288	OMIM:604484	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0003077	PMID:22883144	PCS		3/13			P	HPO:skoehler[2013-09-30];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0003581	PMID:22883144	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0003394	PMID:22883144	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0001284	PMID:22883144	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0002380	PMID:22883144	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0002171	OMIM:604484	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0003074	PMID:22883144	PCS		4/13			P	HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0003380	OMIM:604484	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0008180	OMIM:604484	TAS					P	HPO:skoehler[2012-10-17]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0040078	PMID:22883144	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0009830	OMIM:604484	TAS					P	HPO:probinson[2012-04-11]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0002936	PMID:22883144	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0007126	PMID:22883144	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0003701	PMID:22883144	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0000763	PMID:22883144	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0000006	PMID:22883144	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0003677	PMID:22883144	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2023-02-22]
OMIM:604484	Neuropathy, hereditary motor and sensory, Okinawa type		HP:0002445	OMIM:604484	TAS					P	HPO:probinson[2012-04-11]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0001880	PMID:36884218	PCS		15/16			P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0001047	PMID:36884218	PCS		15/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0003212	PMID:36884218	PCS					P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0004322	PMID:36884218	PCS		7/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0002099	PMID:36884218	PCS		11/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0003593	PMID:36884218	PCS		16/16			C	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0001581	PMID:36884218	PCS		7/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0002020	PMID:36884218	PCS		4/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0410151	PMID:36884218	PCS					P	HPO:probinson[2024-03-12];HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0000939	PMID:36884218	PCS		3/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0032064	PMID:36884218	PCS		10/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0500093	PMID:36884218	PCS		15/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0100845	PMID:36884218	PCS		9/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0012191	PMID:36884218	PCS		1/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0004429	PMID:36884218	PCS		2/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0002205	PMID:36884218	PCS		5/16			P	HPO:probinson[2024-03-12]
OMIM:620532	Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections		HP:0000006	PMID:36884218	PCS					I	HPO:probinson[2024-03-12]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0001419	OMIM:300367	IEA					I	HPO:iea[2009-02-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0003828	OMIM:300367	TAS					M	HPO:skoehler[2012-10-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0001905	OMIM:300367	IEA					P	HPO:iea[2009-02-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0001927	OMIM:300367	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0003593	OMIM:300367	TAS					C	HPO:skoehler[2012-10-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0010972	OMIM:300367	IEA					P	HPO:iea[2009-02-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0000967	OMIM:300367	IEA					P	HPO:iea[2009-02-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0000978	OMIM:300367	IEA					P	HPO:iea[2009-02-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0001934	OMIM:300367	TAS					P	HPO:iea[2009-02-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0000421	OMIM:300367	IEA					P	HPO:iea[2009-02-17]
OMIM:300367	Thrombocytopenia, X-linked, with or without dyserythropoietic anemia		HP:0004447	OMIM:300367	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:616080	Microcephaly 12, primary, autosomal recessive		HP:0000340	PMID:23918663	PCS		10/10			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-12]
OMIM:616080	Microcephaly 12, primary, autosomal recessive		HP:0003577	PMID:23918663	PCS		10/10			C	HPO:probinson[2023-03-12]
OMIM:616080	Microcephaly 12, primary, autosomal recessive		HP:0001250	PMID:23918663	PCS		0/10			P	HPO:probinson[2023-03-12]
OMIM:616080	Microcephaly 12, primary, autosomal recessive		HP:0011451	PMID:23918663	PCS		10/10			P	HPO:probinson[2023-03-12]
OMIM:616080	Microcephaly 12, primary, autosomal recessive		HP:0000007	PMID:23918663	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-12]
OMIM:616080	Microcephaly 12, primary, autosomal recessive		HP:0009879	PMID:23918663	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-12]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0003774	PMID:27466185	PCS		11/12			P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0003621	PMID:17690917	PCS					C	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0005576	PMID:27466185	PCS		4/4			P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0003355	PMID:17690917	PCS					P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0030078	PMID:27466185	PCS	HP:0011462	1/12			P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0002097	PMID:27466185	PCS		3/12			P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0003076	PMID:17690917	PCS					P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0000093	PMID:17690917	PCS					P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0045051	PMID:27466185	PCS					P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0004918	PMID:17690917	PCS					P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0000822	PMID:17690917	PCS	HP:0003621	7/19			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0000007	PMID:27466185	PCS					I	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0002857	PMID:27466185	PCS		12/12			P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0004912	PMID:17690917	PCS		19/19			P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0002206	PMID:27466185	PCS					P	HPO:probinson[2020-08-11]
OMIM:618913	Fanconi renotubular syndrome 5		HP:0002148	PMID:17690917	PCS					P	HPO:probinson[2020-08-11]
OMIM:612580	Intellectual developmental disorder, autosomal dominant 3		HP:0001250	PMID:19012874	PCS		1/5			P	HPO:probinson[2018-06-13]
OMIM:612580	Intellectual developmental disorder, autosomal dominant 3		HP:0000729	PMID:19012874	PCS		1/5			P	HPO:probinson[2018-06-13]
OMIM:612580	Intellectual developmental disorder, autosomal dominant 3		HP:0000006	PMID:19012874	PCS					I	HPO:probinson[2013-04-06]
OMIM:612580	Intellectual developmental disorder, autosomal dominant 3		HP:0001249	PMID:19012874	PCS		5/5			P	HPO:probinson[2013-04-06]
OMIM:190900	TRITANOPIA		HP:0000552	OMIM:190900	IEA					P	HPO:probinson[2009-02-17]
OMIM:190900	TRITANOPIA		HP:0000551	PMID:1531728	PCS					P	HPO:lccarmody[2018-06-29]
OMIM:190900	TRITANOPIA		HP:0008275	OMIM:190900	IEA					P	HPO:iea[2009-02-17]
OMIM:190900	TRITANOPIA		HP:0007641	PMID:1531728	PCS					P	HPO:lccarmody[2018-06-29]
OMIM:190900	TRITANOPIA		HP:0000006	OMIM:190900	IEA					I	HPO:iea[2009-02-17]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000286	PMID:24656866	PCS		2/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000341	PMID:24656866	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0003676	PMID:24656866	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000340	PMID:24656866	PCS		2/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0001252	PMID:24656866	PCS		3/4			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0003593	PMID:24656866	PCS		1/4			C	HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0002119	PMID:24656866	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0003429	PMID:24656866	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000218	PMID:24656866	PCS		2/3			P	HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000358	PMID:24656866	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0006855	PMID:24656866	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0001347	OMIM:615760	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0003623	PMID:24656866	PCS		3/4			C	HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000253	PMID:24656866	PCS		4/4			P	HPO:skoehler[2015-01-21];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0002059	PMID:24656866	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000252	PMID:24656866	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0002133	PMID:24656866	PCS		1/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000431	PMID:24656866	PCS		2/3			P	HPO:probinson[2023-03-30];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0002079	PMID:24656866	PCS					P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0012736	PMID:24656866	PCS		4/4			P	HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0005280	PMID:24656866	PCS		1/3			P	HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000007	PMID:24656866	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000601	PMID:24656866	PCS		2/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0000369	PMID:24656866	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-30]
OMIM:615760	Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy		HP:0009879	PMID:24656866	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-30]
OMIM:610618	Angioedema, hereditary, 3		HP:0005225	PMID:10984376	PCS				HP:0025303	P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-13]
OMIM:610618	Angioedema, hereditary, 3		HP:0100665	PMID:10984376	PCS					P	HPO:probinson[2013-01-09];HPO:probinson[2021-07-13]
OMIM:610618	Angioedema, hereditary, 3		HP:0002574	PMID:10984376	PCS					P	HPO:probinson[2013-02-28];HPO:probinson[2021-07-13]
OMIM:610618	Angioedema, hereditary, 3		HP:0002013	PMID:10984376	PCS				HP:0025303	P	HPO:skoehler[2014-01-28];HPO:probinson[2021-07-13]
OMIM:610618	Angioedema, hereditary, 3		HP:0012271	PMID:10984376	PCS					P	HPO:probinson[2013-04-07];HPO:probinson[2021-07-13]
OMIM:610618	Angioedema, hereditary, 3		HP:0000282	PMID:10984376	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-13]
OMIM:610618	Angioedema, hereditary, 3		HP:0011855	PMID:10984376	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-07-13]
OMIM:610618	Angioedema, hereditary, 3		HP:0000006	PMID:10984376	PCS					I	HPO:probinson[2013-02-28];HPO:probinson[2021-07-13]
OMIM:607364	Bartter syndrome, type 3		HP:0000121	PMID:9326936	PCS		0/17			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0005579	OMIM:607364	IEA					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0003324	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0003577	PMID:9326936	PCS		5/17			C	HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0003621	PMID:9326936	PCS		3/17			C	HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0001960	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0000591	OMIM:607364	IEA					P	HPO:skoehler[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0003593	PMID:9326936	PCS		6/17			C	HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0003081	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0000848	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0000859	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0011463	PMID:9326936	PCS		3/17			C	HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0008046	OMIM:607364	IEA					P	HPO:skoehler[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0001944	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0000007	PMID:9326936	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0000128	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0002914	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0002900	PMID:9326936	PCS		17/17			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0002615	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0000103	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0003127	PMID:9326936	PCS		11/17			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-12]
OMIM:607364	Bartter syndrome, type 3		HP:0000127	OMIM:607364	TAS					P	HPO:skoehler[2013-10-06]
OMIM:607364	Bartter syndrome, type 3		HP:0000610	OMIM:607364	IEA					P	HPO:skoehler[2009-02-17]
OMIM:607364	Bartter syndrome, type 3		HP:0000841	OMIM:607364	IEA					P	HPO:iea[2009-02-17]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0003202	PMID:21617257	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0003676	PMID:21617257	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0002650	PMID:21617257	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0031936	PMID:21617257	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0001332	PMID:21617257	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0001252	PMID:21617257	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0002151	PMID:21617257	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0003593	PMID:21617257	PCS		1/1			C	HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0001290	OMIM:618244	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0002490	PMID:21617257	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0001270	PMID:21617257	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0011923	PMID:21617257	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0000998	PMID:21617257	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0000007	PMID:21617257	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-07-11]
OMIM:618244	Mitochondrial complex I deficiency, nuclear type 23		HP:0001510	PMID:21617257	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0001344	PMID:25704603	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0002540	PMID:25704603	PCS		2/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000343	PMID:25704603	PCS		3/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0001263	PMID:25704603	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0003593	PMID:25704603	PCS		5/5			C	HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0045025	PMID:25704603	PCS		5/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000748	PMID:25704603	PCS		1/5			P	HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000718	PMID:25704603	PCS		3/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000712	PMID:25704603	PCS		3/5			P	HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000007	PMID:25704603	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0002515	PMID:25704603	PCS		3/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000400	PMID:25704603	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0200055	PMID:25704603	PCS		3/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000303	PMID:25704603	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0001337	PMID:25704603	PCS		5/5			P	HPO:probinson[2023-02-20]
OMIM:616269	Intellectual developmental disorder, autosomal recessive 48		HP:0000742	PMID:25704603	PCS		3/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2023-02-20]
OMIM:620903	Polycystic kidney disease 8		HP:0003774	PMID:37598857;PMID:36215968	PCS		13/14			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0003621	PMID:37598857	PCS		3/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0003577	PMID:37598857	PCS		1/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0003596	PMID:37598857	PCS		3/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0004322	PMID:37598857	PCS		2/19			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0000083	PMID:36215968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0003584	PMID:37598857	PCS		1/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0000097	PMID:37598857	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0003593	PMID:36215968	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0000090	PMID:37598857;PMID:36215968	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0001959	PMID:36215968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0011463	PMID:37598857	PCS		4/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0011462	PMID:37598857	PCS		2/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0004719	PMID:36215968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0011461	PMID:37598857	PCS		4/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0000822	PMID:37598857;PMID:36215968	PCS		16/20			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0001712	PMID:37598857	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0001407	PMID:37598857;PMID:36215968	PCS		2/20			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0000103	PMID:36215968	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0000105	PMID:37598857;PMID:36215968	PCS		14/20			P	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0000006	PMID:37598857	PCS					I	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:620903	Polycystic kidney disease 8		HP:0003623	PMID:37598857	PCS		1/19			C	ORCID:0000-0002-0736-9199[2024-12-27]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0100710	OMIM:300830	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0001419	OMIM:300830	TAS					I	HPO:skoehler[2015-12-30]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0001252	OMIM:300830	TAS		HP:0040283			P	HPO:skoehler[2015-11-15]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0000718	OMIM:300830	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0000717	OMIM:300830	TAS		HP:0040280			P	HPO:skoehler[2015-12-30]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0003593	OMIM:300830	TAS					C	HPO:skoehler[2015-12-30]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0001290	OMIM:300830	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0007018	OMIM:300830	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0001249	OMIM:300830	TAS					P	HPO:skoehler[2015-11-15]
OMIM:300830	Autism, susceptibility to, X-linked 4		HP:0100034	OMIM:300830	TAS					P	HPO:skoehler[2015-11-15]
OMIM:618522	Intellectual developmental disorder 59		HP:0002465	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000341	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000486	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0001773	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000343	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0004322	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0001156	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0001250	PMID:23033978	PCS		0/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0003593	PMID:23033978	PCS		1/1			C	HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0001290	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0012368	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0001808	OMIM:618522	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000637	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000411	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000256	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0003502	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0002553	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000297	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0004279	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000750	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0001263	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000348	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000960	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000545	PMID:23033978	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000369	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000006	PMID:23033978	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0000742	PMID:23033978	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618522	Intellectual developmental disorder 59		HP:0004425	OMIM:618522	IEA					P	HPO:skoehler[2019-09-07]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0000253	PMID:20493457	PCS		3/3			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0002059	OMIM:613477	TAS					P	HPO:skoehler[2015-05-31]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0002521	PMID:20493457	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0000252	PMID:20493457	PCS		3/3			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0002510	PMID:20493457	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0002079	PMID:20493457	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0001272	PMID:20493457	PCS		2/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0001250	PMID:20493457	PCS		3/3			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0002120	PMID:20493457	PCS		2/3			P	HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0001252	OMIM:613477	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0003593	PMID:20493457	PCS		3/3			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0002020	PMID:20493457	PCS		2/3			P	HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0001290	OMIM:613477	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0034295	PMID:20493457	PCS		3/3			P	HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0007366	PMID:20493457	PCS		1/3			P	HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0200134	PMID:20493457	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0003429	OMIM:613477	TAS					P	HPO:skoehler[2013-01-21]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0000006	PMID:20493457	PCS					I	HPO:skoehler[2012-12-03];HPO:probinson[2022-10-24]
OMIM:613477	Epileptic encephalopathy, early infantile, 5		HP:0001347	OMIM:613477	TAS					P	HPO:skoehler[2015-05-31]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0002650	PMID:25683117	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0004322	PMID:25683117	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0004440	PMID:25683117	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0001263	PMID:25683117	PCS		0/2			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000691	OMIM:112240	TAS					P	HPO:skoehler[2015-05-31]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0003593	PMID:25683117	PCS		2/2			C	HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:6000871	PMID:25683117	PCS		2/2			P	HPO:probinson[2024-08-03]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0005472	OMIM:112240	IEA					P	HPO:iea[2009-02-17]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0011800	PMID:25683117	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000938	PMID:25683117	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000238	OMIM:112240	IEA					P	HPO:iea[2009-02-17]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0002757	PMID:25683117	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000703	PMID:25683117	PCS		1/2			P	HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0002007	PMID:25683117	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0002953	PMID:25683117	PCS		2/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0002645	PMID:25683117	PCS		1/2			P	HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0001334	PMID:25683117	PCS		2/2		HP:0003676	P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0001620	OMIM:112240	TAS					P	HPO:skoehler[2015-05-31]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000586	OMIM:112240	IEA					P	HPO:iea[2009-02-17]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000520	PMID:25683117	PCS		2/2			P	HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000006	PMID:25683117	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0000347	PMID:25683117	PCS		1/2			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-12-04]
OMIM:112240	Cole-Carpenter syndrome 1		HP:0004349	PMID:25683117	PCS		2/2			P	HPO:probinson[2022-12-04]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0002069	PMID:23252400	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0002476	OMIM:615006	IEA		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0002521	OMIM:615006	IEA		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0002540	OMIM:615006	IEA					P	HPO:skoehler[2018-10-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0002266	PMID:23252400	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0010819	PMID:23252400	PCS		2/4			P	HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0001252	OMIM:615006	IEA		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0003593	PMID:23252400	PCS		4/4			C	HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0032794	PMID:23252400	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0011344	PMID:23252400	PCS		4/4			P	HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0011097	OMIM:615006	IEA		4/4			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0000737	OMIM:615006	IEA		1/1			P	HPO:skoehler[2013-01-11]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0000817	OMIM:615006	IEA		1/1			P	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0032792	PMID:23252400	PCS		1/4			P	HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0000007	PMID:23252400	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2023-03-08]
OMIM:615006	Developmental and epileptic encephalopathy 15		HP:0200134	OMIM:615006	IEA		4/4			P	HPO:skoehler[2015-01-19];HPO:probinson[2023-03-08]
OMIM:601067	Usher syndrome, type ID		HP:0001751	OMIM:601067	TAS					P	HPO:probinson[2009-02-17]
OMIM:601067	Usher syndrome, type ID		HP:0000365	OMIM:601067	TAS	HP:0003577			HP:0012829	P	HPO:probinson[2013-08-12]
OMIM:601067	Usher syndrome, type ID		HP:0000007	OMIM:601067	TAS					I	HPO:probinson[2009-02-17]
OMIM:601067	Usher syndrome, type ID		HP:0000510	OMIM:601067	TAS					P	HPO:probinson[2009-02-17]
OMIM:617605	Deafness, autosomal dominant 71		HP:0003676	PMID:27657680	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2019-06-13]
OMIM:617605	Deafness, autosomal dominant 71		HP:0001751	PMID:27657680	PCS		0/11			P	HPO:probinson[2019-06-13];HPO:probinson[2021-07-03]
OMIM:617605	Deafness, autosomal dominant 71		HP:0000407	PMID:27657680	PCS	HP:0011462	11/11			P	HPO:probinson[2019-06-13];HPO:probinson[2019-06-13]
OMIM:617605	Deafness, autosomal dominant 71		HP:0000006	PMID:27657680	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2019-06-13]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003774	OMIM:618250	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003750	PMID:27374773	PCS		3/3			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0030774	PMID:27374773	PCS		1/1			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0032653	PMID:27374773	PCS		2/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0001508	OMIM:618250	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0011463	PMID:27374773	PCS		1/3			C	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0001627	OMIM:618250	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003648	PMID:27374773	PCS		1/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0025710	PMID:27374773	PCS		1/3			C	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0001324	OMIM:618250	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0001962	PMID:27374773	PCS		1/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003701	PMID:27374773	PCS		2/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003546	PMID:27374773	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003348	PMID:27374773	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003128	PMID:27374773	PCS		1/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003326	OMIM:618250	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003621	PMID:27374773	PCS		1/3			C	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003388	OMIM:618250	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0002013	PMID:27374773	PCS		1/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0002151	PMID:27374773	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0002094	PMID:27374773	PCS		1/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0011923	PMID:27374773	PCS		3/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0012378	PMID:27374773	PCS		1/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0001639	OMIM:618250	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0003738	PMID:27374773	PCS		3/3			P	HPO:probinson[2023-02-22]
OMIM:618250	Mitochondrial complex I deficiency, nuclear type 29		HP:0000007	PMID:27374773	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000365	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002023	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001212	PMID:24431331	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000089	OMIM:309800	TAS					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001250	PMID:24431331	PCS		1/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002021	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001252	OMIM:309800	TAS					P	HPO:skoehler[2014-11-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000482	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001290	PMID:24431331	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000718	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002938	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001647	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0009466	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000678	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0020006	OMIM:309800	TAS					P	HPO:probinson[2015-07-22]
OMIM:309800	Microphthalmia, syndromic 1		HP:0200021	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001249	PMID:24431331	PCS		4/4	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002751	OMIM:309800	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001264	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000692	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000252	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002035	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000690	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0012385	OMIM:309800	TAS					P	HPO:skoehler[2013-10-22]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000528	PMID:24431331	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000729	OMIM:309800	TAS		HP:0040283			P	HPO:skoehler[2014-04-04]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000767	PMID:24431331	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000403	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000568	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002705	OMIM:309800	TAS					P	HPO:skoehler[2015-12-30]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001417	PMID:24431331	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000202	OMIM:309800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000047	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000369	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000204	OMIM:309800	TAS					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000567	OMIM:309800	TAS					P	HPO:probinson[2015-07-19]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001018	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002089	OMIM:309800	TAS		HP:0040283			P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001270	PMID:24431331	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000618	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000612	OMIM:309800	TAS		20/20			P	HPO:probinson[2012-06-10];HPO:iea[2015-07-21]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000218	PMID:24431331	PCS		4/4			P	HPO:skoehler[2014-02-06];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0030084	PMID:24431331	PCS		4/4			P	HPO:skoehler[2014-09-21];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000774	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000894	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0008678	OMIM:309800	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000377	OMIM:309800	TAS					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000396	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002650	PMID:24431331	PCS		4/4			P	HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000072	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0002251	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0009473	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000508	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001159	PMID:24431331	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-08-26]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000465	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0001510	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000028	OMIM:309800	IEA					P	HPO:iea[2009-02-17]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000742	OMIM:309800	TAS					P	HPO:skoehler[2014-02-06]
OMIM:309800	Microphthalmia, syndromic 1		HP:0000588	OMIM:309800	TAS					P	HPO:probinson[2012-06-10]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000682	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0002223	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0004322	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0002164	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000581	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000819	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000958	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0001128	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000677	OMIM:601701	TAS					P	HPO:skoehler[2015-07-26]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0002751	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0003202	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000252	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000175	OMIM:601701	TAS					P	HPO:iea[2012-05-05]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0002552	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0045025	OMIM:601701	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0012385	OMIM:601701	TAS					P	HPO:skoehler[2013-10-22]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0100018	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000968	OMIM:601701	TAS					P	HPO:probinson[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0009473	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000987	OMIM:601701	TAS					P	HPO:probinson[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0001999	OMIM:601701	TAS				HP:0012825	P	HPO:probinson[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000007	OMIM:601701	IEA					I	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0002804	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0007477	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000966	OMIM:601701	TAS					P	HPO:probinson[2012-05-05]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000202	OMIM:601701	IEA					P	HPO:skoehler[2010-06-18]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000204	OMIM:601701	TAS					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000248	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000621	OMIM:601701	IEA					P	HPO:iea[2009-02-17]
OMIM:601701	Arthrogryposis and ectodermal dysplasia		HP:0000962	OMIM:601701	TAS					P	HPO:probinson[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000286	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0008705	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000494	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0001374	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000431	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0002650	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0002561	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0005280	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0002937	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000508	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000316	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000767	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0001537	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000238	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000218	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0002967	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0001159	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0001643	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000006	OMIM:104350	IEA					I	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000369	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0001634	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:104350	Amastia, bilateral, with ureteral triplication and dysmorphism		HP:0000126	OMIM:104350	IEA					P	HPO:iea[2009-02-17]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0002312	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0003621	PMID:12470185;PMID:9931538	PCS		2/2			C	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0002155	OMIM:277460	TAS					P	HPO:probinson[2013-12-15]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001310	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001332	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001288	PMID:12470185	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0003124	OMIM:277460	TAS					P	HPO:probinson[2013-12-15]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0100291	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001272	PMID:12470185	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0030223	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001260	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0003141	OMIM:277460	TAS					P	HPO:probinson[2013-12-15]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001284	OMIM:277460	TAS					P	HPO:skoehler[2009-02-17]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001251	PMID:9931538	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0002075	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0010874	OMIM:277460	TAS					P	HPO:skoehler[2012-10-17]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0002073	PMID:12470185	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0033687	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0010831	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0100513	PMID:12470185;PMID:9931538	PCS		2/2			P	HPO:probinson[2013-12-15];HPO:probinson[2022-04-24];HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0000007	PMID:12470185	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0002403	PMID:9931538	PCS		1/1			P	HPO:probinson[2022-04-24]
OMIM:277460	Ataxia with isolated vitamin E deficiency		HP:0001114	OMIM:277460	TAS					P	HPO:skoehler[2009-02-17]
OMIM:615774	Oocyte maturation defect		HP:0008222	PMID:24670168	PCS		4/4			P	HPO:probinson[2022-03-21]
OMIM:615774	Oocyte maturation defect		HP:0011462	PMID:24670168	PCS		4/4			C	HPO:probinson[2022-03-21]
OMIM:615774	Oocyte maturation defect		HP:0000007	PMID:24670168	PCS					I	HPO:skoehler[2014-05-04];HPO:probinson[2022-03-21]
OMIM:615774	Oocyte maturation defect		HP:6000328	PMID:24670168	PCS		2/2			P	HPO:probinson[2024-02-27]
OMIM:603116	CDAGS syndrome		HP:0000143	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0003577	PMID:15924278	PCS		7/7			C	HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0002023	PMID:15924278	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0004443	PMID:15924278	PCS		2/5			P	HPO:probinson[2012-07-19];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0004442	PMID:15924278	PCS		2/5			P	HPO:probinson[2012-07-19];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0004440	PMID:15924278	PCS		5/5			P	HPO:probinson[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0045075	OMIM:603116	TAS					P	HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0000239	PMID:15924278	PCS		6/6			P	HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0000656	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0200044	PMID:15924278	PCS		2/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0000653	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0000894	PMID:15924278	PCS		5/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0000773	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0000175	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0002697	PMID:15924278	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0000270	OMIM:603116	TAS					P	HPO:probinson[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0001263	PMID:15924278	PCS		4/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0000272	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0011800	OMIM:603116	TAS					P	HPO:skoehler[2013-11-28]
OMIM:603116	CDAGS syndrome		HP:0002808	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0000407	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0000508	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0002209	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0000007	PMID:15924278	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0002007	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0000047	PMID:15924278	PCS		4/4	MALE		P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:603116	CDAGS syndrome		HP:0000248	OMIM:603116	IEA					P	HPO:iea[2009-02-17]
OMIM:603116	CDAGS syndrome		HP:0025407	PMID:15924278	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-05-07]
OMIM:101200	Apert syndrome		HP:0001331	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0002663	PMID:9002682	PCS		1/3			P	HP:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0001177	OMIM:101200	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:101200	Apert syndrome		HP:0000244	PMID:23546041	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000684	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000365	PMID:7668257	PCS		14/35			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000486	PMID:7668257	PCS		23/34			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0004487	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0004443	PMID:9002682	PCS		1/3			P	HP:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0002021	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0004442	PMID:9002682	PCS		1/2			P	HP:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0004440	PMID:9002682	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0010055	PMID:23546041	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0011220	PMID:23546041	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000316	PMID:23546041;PMID:7668257	PCS		37/38			P	ORCID:0000-0002-0736-9199[2024-04-21];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000239	PMID:23546041	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000238	PMID:7668257	PCS		5/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0004635	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0001249	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000358	PMID:23546041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000175	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000494	PMID:23546041	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000453	OMIM:101200	TAS		8/34			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000452	PMID:9002682	PCS		1/2			P	HPO:probinson[2012-04-24];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0002032	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0010554	PMID:23546041	PCS		2/2			P	HPO:probinson[2012-04-24];HPO:probinson[2024-04-21]
OMIM:101200	Apert syndrome		HP:0003041	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0011800	PMID:23546041;PMID:9002682;PMID:7668257	PCS		40/40			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-03-14];ORCID:0000-0002-0736-9199[2024-04-21];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0001061	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:6000807	PMID:25206089	PCS					P	HPO:probinson[2024-08-03]
OMIM:101200	Apert syndrome		HP:0000689	PMID:9002682;PMID:7668257	PCS		11/13			P	HP:probinson[2022-03-14];HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0006101	PMID:7668257	PCS		36/36			P	HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000768	PMID:9002682	PCS		1/2			P	HP:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0002623	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000520	PMID:23546041;PMID:9002682;PMID:7668257	PCS		40/40			P	HP:probinson[2022-03-14];HPO:probinson[2022-03-14];ORCID:0000-0002-0736-9199[2024-04-21];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000006	PMID:23546041	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000248	PMID:9002682	PCS		1/3			P	HP:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000369	PMID:23546041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000126	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0004468	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0003577	PMID:23546041;PMID:9002682	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-04-21];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0001355	OMIM:101200	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000189	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000463	PMID:23546041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0001274	PMID:7668257	PCS		4/36			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0010621	PMID:23546041	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0012725	PMID:9002682	PCS		1/3			P	HP:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0012368	OMIM:101200	TAS					P	HPO:skoehler[2013-10-22]
OMIM:101200	Apert syndrome		HP:6000934	PMID:31145570	PCS					P	HPO:probinson[2024-08-03]
OMIM:101200	Apert syndrome		HP:0001629	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0001507	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0100702	OMIM:101200	IEA					P	HPO:skoehler[2012-10-09]
OMIM:101200	Apert syndrome		HP:0008111	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0007343	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0009642	OMIM:101200	TAS					P	HPO:probinson[2012-04-24]
OMIM:101200	Apert syndrome		HP:0000337	OMIM:101200	TAS					P	HPO:probinson[2012-05-01]
OMIM:101200	Apert syndrome		HP:0000975	PMID:7668257	PCS		23/35			P	HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000219	PMID:23546041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0002119	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000218	PMID:23546041	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0006610	PMID:23546041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0002996	PMID:7668257	PCS		13/36			P	HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0001363	PMID:7668257	IEA		36/36			P	HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0001561	PMID:23546041	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0001321	PMID:7668257	PCS		3/36			P	HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0005048	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0001162	OMIM:101200	TAS		HP:0040283			P	HPO:probinson[2012-04-24]
OMIM:101200	Apert syndrome		HP:0000193	PMID:9002682	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000270	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0004397	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0004991	PMID:7668257	PCS		19/34			P	HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000272	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0005280	PMID:23546041;PMID:9002682	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-21];HP:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0011304	PMID:9002682	PCS		1/2			P	HP:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0007291	OMIM:101200	TAS					P	HPO:probinson[2012-04-24]
OMIM:101200	Apert syndrome		HP:0007099	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000348	OMIM:101200	TAS					P	HPO:probinson[2012-05-01]
OMIM:101200	Apert syndrome		HP:0000389	PMID:7668257	PCS		24/34			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0002007	PMID:23546041	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-21]
OMIM:101200	Apert syndrome		HP:0001159	PMID:9002682	PCS		1/2			P	HP:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000586	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000028	PMID:23546041	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2024-04-21]
OMIM:101200	Apert syndrome		HP:0000303	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:101200	Apert syndrome		HP:0000545	PMID:9002682	PCS		1/2			P	HP:probinson[2022-03-14];HPO:probinson[2022-03-14]
OMIM:101200	Apert syndrome		HP:0000148	OMIM:101200	IEA					P	HPO:iea[2009-02-17]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0025066	OMIM:618278	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0004445	OMIM:618278	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0000486	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001332	PMID:29423877;PMID:32435055	PCS		4/4			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16];HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001250	PMID:29423877	PCS		2/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002240	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001270	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0100750	PMID:32435055	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0012444	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0033725	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001508	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002719	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0000737	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0000817	PMID:29423877	PCS		3/3			P	HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001404	OMIM:618278	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002878	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002119	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001923	OMIM:618278	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0004315	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0003623	PMID:29423877;PMID:32435055	PCS		4/4			C	HPO:probinson[2022-03-16];HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002014	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0008936	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001640	PMID:29423877;PMID:32435055	PCS		2/4			P	HPO:probinson[2022-03-19];HPO:skoehler[2019-04-18];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002079	OMIM:618278	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0011968	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0004870	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001263	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002093	PMID:29423877	PCS		3/3			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0011273	OMIM:618278	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0008282	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0003819	PMID:29423877	PCS		3/3			C	HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001878	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0000767	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0000007	PMID:29423877	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0000505	PMID:29423877	PCS		3/3			P	HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001714	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002205	PMID:29423877	PCS		3/3			P	HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001433	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002206	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002789	OMIM:618278	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001414	PMID:29423877	PCS		1/3			P	HPO:probinson[2022-03-16]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0002445	OMIM:618278	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001974	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0001336	PMID:32435055	PCS		1/1			P	HPO:probinson[2022-03-19]
OMIM:618278	Fibrosis, neurodegeneration, and cerebral angiomatosis		HP:0004447	OMIM:618278	IEA					P	HPO:skoehler[2019-02-15]
OMIM:185100	Strabismus, susceptibility to		HP:0031724	OMIM:185100	IEA					P	HPO:skoehler[2018-10-08]
OMIM:185100	Strabismus, susceptibility to		HP:0000486	OMIM:185100	IEA					P	HPO:iea[2009-02-17]
OMIM:616255	Short stature with nonspecific skeletal abnormalities		HP:0002750	OMIM:616255	TAS		HP:0040283			P	HPO:skoehler[2015-12-30]
OMIM:616255	Short stature with nonspecific skeletal abnormalities		HP:0003508	PMID:16384845	PCS		16/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-02]
OMIM:616255	Short stature with nonspecific skeletal abnormalities		HP:0000006	PMID:16384845	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-02]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0002510	PMID:19465911	PCS		7/7			P	HPO:probinson[2021-02-27]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0002376	PMID:19465911	PCS		7/7		HP:0025215	P	HPO:probinson[2021-02-27]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0000737	PMID:19465911	PCS		3/7			P	HPO:probinson[2021-02-27]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0002352	PMID:19465911	PCS		6/6			P	HPO:probinson[2021-02-27]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0003593	PMID:19465911	PCS		7/7			C	HPO:probinson[2021-02-27]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0012708	PMID:19465911	PCS					P	HPO:probinson[2021-02-27]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0000007	PMID:19465911	PCS					I	HPO:probinson[2021-02-27];HPO:probinson[2021-02-27]
OMIM:619166	Mitochondrial complex II deficiency, nuclear type 2		HP:0001510	PMID:19465911	PCS		6/7			P	HPO:probinson[2021-02-27]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0000490	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0000160	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0000272	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0004691	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0010442	PMID:21937992;PMID:19797195	PCS		9/9			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-08-30];HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0005280	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0100259	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0000316	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0000007	PMID:21937992	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0030084	PMID:31469663	PCS		2/2			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0000510	PMID:31469663;PMID:19797195	PCS		6/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-08-30];HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0000135	PMID:31469663;PMID:19797195	PCS		5/5			P	HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0001513	PMID:21937992;PMID:31469663;PMID:19797195	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-08-30];HPO:probinson[2021-08-30]
OMIM:615984	Bardet-Biedl syndrome 7		HP:0001249	PMID:21937992;PMID:31469663	PCS		6/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-08-30];HPO:probinson[2021-08-30]
OMIM:614324	Ovarian dysgenesis 3		HP:0003621	PMID:21963259	PCS		3/3			C	HPO:probinson[2022-06-11]
OMIM:614324	Ovarian dysgenesis 3		HP:0010463	PMID:21963259	PCS		3/3			P	HPO:probinson[2022-06-11]
OMIM:614324	Ovarian dysgenesis 3		HP:0011969	PMID:21963259	PCS		3/3			P	HPO:probinson[2022-06-11];HPO:probinson[2022-06-11]
OMIM:614324	Ovarian dysgenesis 3		HP:0008222	PMID:21963259	PCS					P	HPO:probinson[2022-06-11];HPO:probinson[2022-06-11]
OMIM:614324	Ovarian dysgenesis 3		HP:0008232	PMID:21963259	PCS		3/3			P	HPO:probinson[2022-06-11];HPO:probinson[2022-06-11]
OMIM:614324	Ovarian dysgenesis 3		HP:0000007	PMID:21963259	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:614324	Ovarian dysgenesis 3		HP:0000823	PMID:21963259	PCS		3/3			P	HPO:probinson[2022-06-11]
OMIM:614324	Ovarian dysgenesis 3		HP:0000786	PMID:21963259	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-06-11]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0002015	PMID:17439987	PCS		2/15			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0001762	OMIM:181400	IEA					P	HPO:iea[2009-02-17]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0003596	PMID:17439987	PCS		5/13			C	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0000771	PMID:17439987	PCS		3/9	MALE		P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0030319	PMID:17439987	PCS		2/15			P	HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0011462	PMID:17439987	PCS		8/13			C	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0009027	PMID:17439987	PCS		2/15			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0009049	PMID:17439987	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0003805	PMID:17439987	PCS		6/8			P	HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0003704	PMID:17439987	PCS		13/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0003724	PMID:17439987	PCS		13/15			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0020203	PMID:17439987	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:181400	Scapuloperoneal syndrome, neurogenic, Kaeser type		HP:0000006	PMID:17439987	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0003676	OMIM:605229	IEA					C	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0001761	OMIM:605229	IEA					P	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0003487	OMIM:605229	IEA					P	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0007340	OMIM:605229	IEA					P	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0003581	OMIM:605229	TAS					C	HPO:probinson[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0002064	OMIM:605229	IEA					P	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0002061	OMIM:605229	IEA					P	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0007002	OMIM:605229	IEA					P	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0000007	OMIM:605229	IEA					I	HPO:iea[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0001258	OMIM:605229	TAS					P	HPO:probinson[2009-02-17]
OMIM:605229	Spastic paraplegia 14, autosomal recessive		HP:0001347	OMIM:605229	IEA					P	HPO:iea[2009-02-17]
OMIM:148600	Keratoderma, palmoplantar, punctate type IA		HP:0001595	PMID:28239884	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:148600	Keratoderma, palmoplantar, punctate type IA		HP:0001597	PMID:28239884	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:148600	Keratoderma, palmoplantar, punctate type IA		HP:0003596	PMID:28239884	PCS		1/3			C	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:148600	Keratoderma, palmoplantar, punctate type IA		HP:0006482	PMID:28239884	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:148600	Palmoplantar keratoderma, punctate type IA		HP:0025114	PMID:23064416	PCS					P	HP:probinson[2019-04-13]
OMIM:148600	Keratoderma, palmoplantar, punctate type IA		HP:0011462	PMID:28239884	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-05-25]
OMIM:148600	Palmoplantar keratoderma, punctate type IA		HP:0025092	PMID:23064416	PCS					P	HP:probinson[2019-04-13];HP:probinson[2019-04-13]
OMIM:148600	Palmoplantar keratoderma, punctate type IA		HP:0007530	PMID:23064416	PCS		3/3			P	HP:probinson[2019-04-13]
OMIM:148600	Palmoplantar keratoderma, punctate type IA		HP:0040162	PMID:23064416	PCS					P	HP:probinson[2019-04-13]
OMIM:148600	Palmoplantar keratoderma, punctate type IA		HP:0000006	PMID:23064416	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-04-13]
OMIM:264420	Fundus dystrophy, pseudoinflammatory, recessive form		HP:0007769	OMIM:264420	IEA					P	HPO:iea[2009-02-17]
OMIM:264420	Fundus dystrophy, pseudoinflammatory, recessive form		HP:0000573	OMIM:264420	IEA					P	HPO:iea[2009-02-17]
OMIM:264420	Fundus dystrophy, pseudoinflammatory, recessive form		HP:0000529	OMIM:264420	TAS					P	HPO:probinson[2013-04-08]
OMIM:264420	Fundus dystrophy, pseudoinflammatory, recessive form		HP:0000007	OMIM:264420	IEA					I	HPO:iea[2009-02-17]
OMIM:264420	Fundus dystrophy, pseudoinflammatory, recessive form		HP:0007641	OMIM:264420	IEA					P	HPO:iea[2009-02-17]
OMIM:264420	Fundus dystrophy, pseudoinflammatory, recessive form		HP:0000545	OMIM:264420	IEA					P	HPO:iea[2009-02-17]
OMIM:264420	Fundus dystrophy, pseudoinflammatory, recessive form		HP:0007822	OMIM:264420	IEA					P	HPO:iea[2009-02-17]
OMIM:300818	Paroxysmal nocturnal hemoglobinuria		HP:0001442	PMID:8306954	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2022-08-17]
OMIM:300818	Paroxysmal nocturnal hemoglobinuria		HP:0003581	PMID:25244093	PCS					C	HPO:probinson[2022-08-17]
OMIM:300818	Paroxysmal nocturnal hemoglobinuria		HP:0004818	PMID:8306954	PCS					P	HPO:skoehler[2012-10-14];HPO:probinson[2022-08-17]
OMIM:619614	Retinitis pigmentosa 92		HP:0001133	PMID:30085091	PCS		1/1			P	HPO:probinson[2022-01-31]
OMIM:619614	Retinitis pigmentosa 92		HP:0003596	PMID:30085091	PCS		1/2			C	HPO:probinson[2022-01-31]
OMIM:619614	Retinitis pigmentosa 92		HP:0000662	PMID:30085091	PCS		2/2			P	HPO:probinson[2022-01-31]
OMIM:619614	Retinitis pigmentosa 92		HP:0011462	PMID:30085091	PCS		1/2			C	HPO:probinson[2022-01-31]
OMIM:619614	Retinitis pigmentosa 92		HP:0000580	PMID:30085091	PCS		2/2			P	HPO:probinson[2022-01-31]
OMIM:619614	Retinitis pigmentosa 92		HP:0000007	PMID:30085091	PCS					I	HPO:probinson[2022-01-31]
OMIM:619614	Retinitis pigmentosa 92		HP:0000505	PMID:30085091	PCS		2/2			P	HPO:probinson[2022-01-31]
OMIM:619614	Retinitis pigmentosa 92		HP:0030528	PMID:30085091	PCS		1/1			P	HPO:probinson[2022-01-31]
OMIM:617639	Deafness, autosomal recessive 107		HP:0000365	PMID:26881968	PCS	HP:0003593	2/2			P	HPO:probinson[2019-06-13]
OMIM:617639	Deafness, autosomal recessive 107		HP:0000007	PMID:26881968	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-06-13]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0000054	PMID:16493448	PCS			MALE		P	HPO:iea[2009-02-17];HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0000750	PMID:16493448	PCS		14/14			P	HPO:probinson[2012-07-22];HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0000662	PMID:16493448	PCS	HP:0003593				P	HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0008915	PMID:16493448	PCS	HP:0011463	14/14			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0001252	PMID:16493448	PCS		0/14			P	HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0003593	PMID:16493448	PCS					C	HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0000518	PMID:16493448	PCS	HP:0003621				P	HPO:iea[2009-02-17]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0000007	PMID:16493448	PCS					I	HPO:iea[2009-02-17]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0007663	PMID:16493448	PCS	HP:0011463				P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0001956	PMID:16493448	PCS	HP:0011463				P	HPO:iea[2009-02-17]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0001257	PMID:16493448	PCS		0/14			P	HPO:probinson[2023-03-31]
OMIM:610156	Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome		HP:0000556	PMID:16493448	PCS					P	HPO:probinson[2015-07-20];HPO:probinson[2023-03-31]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003687	PMID:17761684	PCS		1/1			P	HPO:probinson[2023-03-18]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003236	PMID:17761684	PCS		1/1			P	HPO:probinson[2012-04-11]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003621	PMID:17761684	PCS		1/1			C	HPO:probinson[2023-03-18]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003198	PMID:17761684	PCS		1/1			P	HPO:probinson[2023-03-18]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003691	PMID:17761684	PCS		1/1			P	HPO:probinson[2023-03-18]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003560	OMIM:612999	TAS					P	HPO:skoehler[2013-05-29]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0011675	OMIM:612999	TAS					P	HPO:probinson[2012-04-11]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0002093	PMID:17761684	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0011463	OMIM:612999	TAS					C	HPO:probinson[2012-04-11]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0001638	OMIM:612999	TAS					P	HPO:probinson[2012-04-11]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0007126	OMIM:612999	TAS					P	HPO:probinson[2012-04-11]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003701	OMIM:612999	TAS					P	HPO:probinson[2012-04-11]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0000006	PMID:17761684	PCS					I	HPO:probinson[2012-04-11];HPO:probinson[2023-03-18]
OMIM:612999	Emery-Dreifuss muscular dystrophy 5, autosomal dominant		HP:0003557	PMID:17761684	PCS		1/1			P	HPO:probinson[2023-03-18]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0000385	PMID:2669480	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0000431	PMID:2669480	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0000083	PMID:2669480	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0011220	PMID:2669480	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0008551	PMID:2669480	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0000007	OMIM:236400	IEA					I	HPO:iea[2009-02-17]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0003041	OMIM:236400	IEA					P	HPO:iea[2009-02-17]
OMIM:236400	Humeroradial synostosishumeroradial/multiple synostosis syndrome		HP:0000248	PMID:2669480	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000175	PMID:24219130;PMID:12165566;PMID:9697705;PMID:35963604;PMID:16882747	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-10];ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0003577	PMID:24219130;PMID:12165566;PMID:9697705;PMID:35963604;PMID:16882747	PCS		7/7			C	ORCID:0000-0002-0736-9199[2024-04-30];HPO:probinson[2023-06-10]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0001561	OMIM:241850	IEA					P	HPO:iea[2009-02-17]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000453	PMID:24219130;PMID:12165566;PMID:16882747	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0031507	PMID:12165566;PMID:9697705;PMID:16882747	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0002750	PMID:12165566	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0011968	PMID:24219130;PMID:35963604	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0001263	PMID:12165566;PMID:9697705;PMID:35963604	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:6000244	PMID:16882747	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0010564	PMID:24219130;PMID:12165566;PMID:9697705;PMID:35963604;PMID:16882747	PCS		2/7			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-06-10];ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0430050	PMID:12165566;PMID:35963604	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0008191	PMID:24219130;PMID:12165566;PMID:9697705;PMID:35963604;PMID:16882747	PCS		8/9			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-10];ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0100786	PMID:24219130	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000316	PMID:12165566	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000007	PMID:9697705	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-10]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0002925	PMID:12165566;PMID:16882747	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000821	PMID:24219130;PMID:12165566;PMID:9697705;PMID:35963604;PMID:16882747	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000851	PMID:9697705	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000369	PMID:24219130;PMID:12165566;PMID:9697705;PMID:35963604;PMID:16882747	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0000358	PMID:24219130;PMID:12165566;PMID:9697705;PMID:35963604;PMID:16882747	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-04-30]
OMIM:241850	Bamforth-Lazarus syndrome		HP:0004502	PMID:9697705	PCS		2/2			P	HPO:probinson[2023-06-10]
OMIM:614456	Melanoma, cutaneous malignant, susceptibility to, 8		HP:0012056	PMID:22080950	PCS					P	HPO:probinson[2013-01-09]
OMIM:614456	Melanoma, cutaneous malignant, susceptibility to, 8		HP:0000006	PMID:22080950	PCS					I	HPO:probinson[2013-08-10]
OMIM:613339	Epilepsy, hot water, 1		HP:0003621	OMIM:613339	IEA					C	HPO:skoehler[2010-06-19]
OMIM:613339	Epilepsy, hot water, 1		HP:0002373	OMIM:613339	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:613339	Epilepsy, hot water, 1		HP:0001252	OMIM:613339	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613339	Epilepsy, hot water, 1		HP:0003829	OMIM:613339	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613339	Epilepsy, hot water, 1		HP:0001290	OMIM:613339	TAS					P	HPO:skoehler[2017-07-13]
OMIM:613339	Epilepsy, hot water, 1		HP:0002329	OMIM:613339	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613339	Epilepsy, hot water, 1		HP:0000006	OMIM:613339	IEA					I	HPO:skoehler[2010-06-19]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0007737	PMID:24608809	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0001263	PMID:18327255	PCS		5/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-14]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0000007	PMID:18327255	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-14]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0010442	PMID:18327255;PMID:24608809	PCS		8/8			P	HPO:probinson[2021-02-14];HPO:skoehler[2014-11-26];HPO:probinson[2021-02-14]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0000510	PMID:18327255;PMID:24608809	PCS		7/8			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14];HPO:skoehler[2014-11-26];HPO:probinson[2021-02-14]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0007843	PMID:24608809	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0001249	PMID:18327255	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-14]
OMIM:615990	Bardet-Biedl syndrome 13		HP:0001513	PMID:18327255;PMID:24608809	PCS		8/8			P	HPO:probinson[2021-02-14];HPO:skoehler[2014-11-26];HPO:probinson[2021-02-14]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000132	PMID:32565547	PCS		1/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0001022	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000486	PMID:32565547	PCS		1/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0002286	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0012805	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0033535	PMID:32565547	IEA		2/2			P	HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000639	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0008320	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0007750	PMID:32565547	PCS		1/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000613	PMID:32565547	PCS		1/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000007	PMID:32565547	PCS					I	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0007663	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0001107	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000978	PMID:32565547	PCS		1/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000421	PMID:32565547	PCS		2/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000225	PMID:32565547	PCS		1/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:619172	Hermansky-Pudlak syndrome 11		HP:0000995	PMID:32565547	PCS		1/2			P	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:618287	Autoinflammatory disease, familial, Behcet-like-3		HP:0000155	PMID:28600438	PCS		4/4			P	HPO:probinson[2019-09-07];HPO:probinson[2019-10-04]
OMIM:618287	Autoinflammatory disease, familial, Behcet-like-3		HP:0002719	PMID:28600438	PCS		0/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2019-09-07];HPO:probinson[2024-03-15]
OMIM:618287	Autoinflammatory disease, familial, Behcet-like-3		HP:0032564	PMID:28600438	PCS		1/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2019-09-07];HPO:probinson[2019-10-04]
OMIM:618287	Autoinflammatory disease, familial, Behcet-like-3		HP:0032565	PMID:28600438	PCS		1/3	FEMALE		P	HPO:probinson[2019-09-07];HPO:probinson[2019-10-04]
OMIM:618287	Autoinflammatory disease, familial, Behcet-like-3		HP:0000006	PMID:28600438	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2019-09-07]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001177	PMID:37384395	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0002023	PMID:37384395	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000262	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0003097	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001274	PMID:37384395	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0410030	PMID:37619988;PMID:37384395	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000180	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001629	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0008551	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000316	PMID:37384395	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000337	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0006695	PMID:37619988;PMID:37384395	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0006159	PMID:37384395	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001841	PMID:37384395	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000278	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000256	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000175	PMID:37619988;PMID:37384395	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001561	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001660	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000431	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001321	PMID:37384395	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001162	PMID:37619988;PMID:37384395	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0010112	PMID:37384395	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0033183	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0034199	PMID:37619988	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0010880	PMID:37619988	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0034198	PMID:37384395	PCS		4/4			C	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000007	PMID:37384395	PCS					I	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0001830	PMID:37619988;PMID:37384395	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000664	PMID:37384395	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000347	PMID:37619988;PMID:37384395	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:620718	Orofaciodigital syndrome XX		HP:0000369	PMID:37619988;PMID:37384395	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-30]
OMIM:239900	Hypertrophic neuropathy and cataract		HP:0000518	OMIM:239900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:239900	Hypertrophic neuropathy and cataract		HP:0009830	OMIM:239900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:239900	Hypertrophic neuropathy and cataract		HP:0000007	OMIM:239900	TAS					I	HPO:skoehler[2009-02-17]
OMIM:239900	Hypertrophic neuropathy and cataract		HP:0002936	OMIM:239900	TAS					P	HPO:skoehler[2013-03-24]
OMIM:239900	Hypertrophic neuropathy and cataract		HP:0002922	OMIM:239900	TAS					P	HPO:skoehler[2009-02-17]
OMIM:203450	Alexander disease		HP:0001310	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0002483	OMIM:203450	TAS					P	HPO:probinson[2009-02-17]
OMIM:203450	Alexander disease		HP:0001250	OMIM:203450	IEA					P	HPO:iea[2009-02-17]
OMIM:203450	Alexander disease		HP:0003593	PMID:11138011;OMIM:203450	PCS		19/21			C	HPO:probinson[2009-02-17];HPO:probinson[2022-05-10]
OMIM:203450	Alexander disease		HP:0001251	PMID:17438228	PCS		1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0004481	OMIM:203450	IEA					P	HPO:iea[2009-02-17]
OMIM:203450	Alexander disease		HP:0007162	OMIM:203450	IEA					P	HPO:iea[2009-02-17]
OMIM:203450	Alexander disease		HP:0011463	PMID:11138011	PCS		1/11			C	HPO:probinson[2022-05-10];HPO:probinson[2022-05-10]
OMIM:203450	Alexander disease		HP:0000238	OMIM:203450	IEA					P	HPO:iea[2009-02-17]
OMIM:203450	Alexander disease		HP:0025710	PMID:17438228	PCS		1/1			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0001522	PMID:11138011	PCS		2/11			C	HPO:probinson[2022-05-10]
OMIM:203450	Alexander disease		HP:0003621	PMID:11138011	PCS		1/11			C	HPO:probinson[2022-05-10]
OMIM:203450	Alexander disease		HP:0002376	OMIM:203450	TAS					P	HPO:probinson[2009-02-17]
OMIM:203450	Alexander disease		HP:0003487	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0001260	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0011421	PMID:11138011	PCS		5/11			C	HPO:probinson[2022-05-10]
OMIM:203450	Alexander disease		HP:0010530	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0100321	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0012378	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0025492	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0003819	PMID:11138011	PCS		1/11			C	HPO:probinson[2022-05-10]
OMIM:203450	Alexander disease		HP:0012043	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0002922	OMIM:203450	IEA					P	HPO:iea[2009-02-17]
OMIM:203450	Alexander disease		HP:0002329	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0000741	PMID:17438228	PCS		1/1			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:203450	Alexander disease		HP:0001257	OMIM:203450	IEA					P	HPO:iea[2009-02-17]
OMIM:203450	Alexander disease		HP:0000006	PMID:11138011	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-10]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0002069	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0002067	PMID:33414379	PCS		2/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0001250	PMID:33414379	PCS		5/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0003593	PMID:33414379	PCS		4/9			C	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0012169	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000719	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0007164	PMID:33414379	PCS		3/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0011463	PMID:33414379	PCS		2/9			C	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000718	PMID:33414379	PCS		6/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0012471	PMID:33414379	PCS		2/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000953	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0020045	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0012170	PMID:33414379	PCS		2/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000752	PMID:33414379	PCS		2/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0001302	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0001249	PMID:33414379	PCS		11/12			P	HPO:probinson[2022-07-17];HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000252	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0003621	PMID:33414379	PCS		3/9			C	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0002354	PMID:33414379	PCS		3/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0002197	PMID:33414379	PCS		3/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0001263	PMID:33414379	PCS		6/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000709	PMID:33414379	PCS		3/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0011198	PMID:33414379	PCS		2/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0001339	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000007	PMID:28397838	PCS					I	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0100716	PMID:33414379	PCS		2/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000565	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0007018	PMID:33414379	PCS		5/12			P	HPO:probinson[2022-07-17]
OMIM:619827	Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly		HP:0000787	PMID:33414379	PCS		1/12			P	HPO:probinson[2022-07-17]
OMIM:274800	Thyroid hormonogenesis, genetic defect in, 4		HP:0000007	OMIM:274800	IEA					I	HPO:iea[2009-02-17]
OMIM:274800	Thyroid hormonogenesis, genetic defect in, 4		HP:0000821	OMIM:274800	IEA					P	HPO:iea[2009-02-17]
OMIM:274800	Thyroid hormonogenesis, genetic defect in, 4		HP:0001510	OMIM:274800	IEA					P	HPO:iea[2009-02-17]
OMIM:274800	Thyroid hormonogenesis, genetic defect in, 4		HP:0000853	OMIM:274800	IEA					P	HPO:iea[2009-02-17]
OMIM:274800	Thyroid hormonogenesis, genetic defect in, 4		HP:0001249	OMIM:274800	IEA					P	HPO:iea[2009-02-17]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0010804	PMID:35108495	PCS		2/8			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0002188	PMID:35108495	PCS		2/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000486	PMID:35108495	PCS		2/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000365	PMID:35108495	PCS		1/7			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0004322	PMID:35108495	PCS		2/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0002263	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0008807	PMID:35108495	PCS		1/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001252	PMID:35108495	PCS		4/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0003196	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001251	PMID:35108495	PCS		2/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0002020	PMID:35108495	PCS		1/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000280	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0033725	PMID:35108495	PCS		2/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000518	PMID:35108495	PCS		2/8			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000718	PMID:35108495	PCS		1/5			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0007165	PMID:35108495	PCS		1/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000316	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000238	PMID:35108495	PCS		1/9			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000358	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001249	PMID:35108495	PCS		3/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001601	PMID:35108495	PCS		1/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001765	PMID:35108495	PCS		2/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000252	PMID:35108495	PCS		3/6			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001385	PMID:35108495	PCS		3/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000574	PMID:35108495	PCS		2/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000331	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0002673	PMID:35108495	PCS		1/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001263	PMID:35108495	PCS		4/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0100021	PMID:35108495	PCS		3/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000007	PMID:35108495	PCS					I	HPO:probinson[2022-06-26]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000527	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000648	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000341	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03];HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0003577	PMID:35108495	PCS		8/10			C	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000582	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000541	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0010747	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0002002	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001270	PMID:35108495	PCS		3/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001508	PMID:35108495	PCS		2/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000737	PMID:35108495	PCS		2/5			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0100702	PMID:35108495	PCS		1/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0006970	PMID:35108495	PCS		2/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0002119	PMID:35108495	PCS		2/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000218	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0007108	PMID:35108495	PCS		1/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0003621	PMID:35108495	PCS		1/10			C	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001561	PMID:35108495	PCS		2/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0002650	PMID:35108495	PCS		5/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000276	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0030048	PMID:35108495	PCS		1/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001761	PMID:35108495	PCS		3/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0005684	PMID:35108495	PCS		1/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0005280	PMID:35108495	PCS		2/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0011471	PMID:35108495	PCS		2/9			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0025708	PMID:35108495	PCS		1/10			C	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000629	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0033683	PMID:35108495	PCS		1/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0100716	PMID:35108495	PCS		2/5			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001511	PMID:35108495	PCS		1/10			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0001357	PMID:35108495	PCS		1/8			P	HPO:probinson[2022-07-03]
OMIM:619833	Neurodevelopmental disorder with neuromuscular and skeletal abnormalities		HP:0000347	PMID:35108495	PCS		3/8			P	HPO:probinson[2022-07-03]
OMIM:307150	Hypertrichosis, congenital generalized		HP:0002650	PMID:21636067	PCS		HP:0040283	MALE		P	HPO:skoehler[2013-06-03];HPO:probinson[2023-02-12]
OMIM:307150	Hypertrichosis, congenital generalized		HP:0004540	PMID:21636067	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:307150	Hypertrichosis, congenital generalized		HP:0001423	PMID:21636067	PCS					I	HPO:skoehler[2013-05-29];HPO:probinson[2023-02-12]
OMIM:307150	Hypertrichosis, congenital generalized		HP:0001007	PMID:21636067	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-12]
OMIM:243060	Male infertility with large-headed, multiflagellar, polyploid spermatozoa		HP:0034309	PMID:21733974	PCS		2/2			P	HPO:probinson[2022-09-05]
OMIM:243060	Male infertility with large-headed, multiflagellar, polyploid spermatozoa		HP:0003251	PMID:17435757	PCS		16/16			P	HPO:probinson[2022-08-04];HPO:skoehler[2010-06-20];HPO:probinson[2022-08-04]
OMIM:243060	Male infertility with large-headed, multiflagellar, polyploid spermatozoa		HP:0011462	PMID:17435757	PCS		2/2			C	HPO:probinson[2022-08-04]
OMIM:243060	Male infertility with large-headed, multiflagellar, polyploid spermatozoa		HP:0000007	PMID:17435757	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-04]
OMIM:243060	Male infertility with large-headed, multiflagellar, polyploid spermatozoa		HP:0025437	PMID:17435757	PCS		2/2			P	HPO:probinson[2022-08-04]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0000660	PMID:19304573	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0002155	PMID:17883852;PMID:19304573	PCS		3/3			P	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0003233	PMID:19304573	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0003563	PMID:19304573	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0001013	PMID:19304573	PCS		0/1			P	HPO:probinson[2022-03-08];HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0002583	OMIM:615947	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0002240	PMID:19304573	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0005181	PMID:17883852	PCS		1/2			P	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0012238	PMID:17883852;PMID:19304573	PCS		3/3			P	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0025708	PMID:17883852	PCS		2/2			C	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0100027	PMID:17883852	PCS		2/2			P	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0001508	PMID:19304573	PCS		1/1			P	HPO:skoehler[2014-08-24];HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0010980	PMID:17883852	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0011463	PMID:19304573	PCS		1/1			C	HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0000007	PMID:17883852	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0001744	PMID:19304573	PCS		1/1			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-08]
OMIM:615947	Hyperlipoproteinemia, type ID		HP:0001733	PMID:19304573	PCS		0/1			P	HPO:probinson[2022-03-08];HPO:probinson[2022-03-08]
OMIM:131300	Camurati-Engelmann disease		HP:0000365	PMID:15894597	IEA		10/67			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:131300	Camurati-Engelmann disease		HP:0003034	OMIM:131300	TAS					P	HPO:iea[2009-02-17];HPO:probinson[2024-08-04]
OMIM:131300	Camurati-Engelmann disease		HP:0001293	PMID:20301335	PCS	HP:0003581				P	HPO:iea[2009-12-02];HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0005791	PMID:15894597	IEA		21/22			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:131300	Camurati-Engelmann disease		HP:0032458	PMID:15894597	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2019-04-20]
OMIM:131300	Camurati-Engelmann disease		HP:0011001	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0001903	PMID:20301335	PCS		HP:0040283			P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0009763	PMID:15894597	IEA		63/92			P	HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:131300	Camurati-Engelmann disease		HP:0002515	PMID:20301335;PMID:15894597	PCS		54/102			P	HPO:iea[2009-02-17];HP:probinson[2019-03-09];HPO:probinson[2019-04-20]
OMIM:131300	Camurati-Engelmann disease		HP:0002857	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0001324	PMID:29620655;PMID:15894597	PCS		40/96			P	HP:probinson[2019-03-09];HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:131300	Camurati-Engelmann disease		HP:0002315	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0005528	OMIM:131300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:131300	Camurati-Engelmann disease		HP:0003202	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:6001056	PMID:15326622	PCS					P	HPO:probinson[2024-08-04]
OMIM:131300	Camurati-Engelmann disease		HP:0003621	PMID:15894597	IEA					C	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0000670	PMID:20301335	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0002650	PMID:20301335;PMID:29620655	PCS		12/14			P	HP:probinson[2019-03-09];HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0002694	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0000651	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0003388	PMID:29620655;PMID:15894597	PCS		36/76			P	HP:probinson[2019-03-09];HPO:iea[2009-02-17];HPO:probinson[2019-04-20]
OMIM:131300	Camurati-Engelmann disease		HP:0007807	PMID:20301335	PCS					P	HPO:iea[2009-02-17];HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0004396	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0012514	PMID:29620655	PCS		4/4			P	HPO:skoehler[2019-02-22];HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0003758	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0000823	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0001533	PMID:15894597	IEA					P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0000520	PMID:15894597	IEA	HP:0003581				P	HPO:iea[2009-02-17]
OMIM:131300	Camurati-Engelmann disease		HP:0000520	PMID:29620655	PCS		2/4			P	HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0000303	PMID:20301335	PCS	HP:0003581				P	HPO:iea[2009-12-02];HP:probinson[2019-03-09]
OMIM:131300	Camurati-Engelmann disease		HP:0000006	PMID:15894597	IEA					I	HPO:iea[2009-02-17]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0008936	PMID:27616480	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0001276	PMID:27616480	PCS		16/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0000252	PMID:27616480	PCS		3/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0002540	PMID:27616480	PCS		3/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0001344	PMID:27616480	PCS		9/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0002123	PMID:27616480	PCS		4/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0031936	PMID:27616480	PCS		13/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0002373	PMID:27616480	PCS		2/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0002197	PMID:27616480	PCS		1/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0001250	PMID:27616480	PCS		10/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0001263	PMID:27616480	PCS		16/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0003593	PMID:27616480	PCS					C	HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0001290	PMID:27616480	PCS	HP:0003593	15/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0000729	PMID:27616480	PCS		7/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0000007	PMID:27616480	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0007359	PMID:27616480	PCS		1/16			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0002126	PMID:27616480	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0001249	PMID:27616480	PCS		16/16			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-03]
OMIM:617188	Intellectual developmental disorder, autosomal recessive 57		HP:0001347	PMID:27616480	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-03]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0003455	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000286	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0007759	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000582	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0003355	OMIM:214110	IEA					P	HPO:skoehler[2010-06-20]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001250	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001252	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000262	OMIM:214110	TAS					P	HPO:probinson[2012-05-01]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0002240	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000580	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0011039	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001290	OMIM:214110	TAS					P	HPO:skoehler[2017-07-13]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001093	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0012103	OMIM:214110	TAS					P	HPO:skoehler[2013-06-13]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000518	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001508	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000316	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000778	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000239	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000954	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0030680	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001627	OMIM:214110	TAS					P	HPO:skoehler[2015-12-30]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001401	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001840	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000113	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001249	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000952	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001088	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000175	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001762	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0002033	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001284	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0100540	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0012385	OMIM:214110	TAS					P	HPO:skoehler[2013-10-22]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0003819	OMIM:214110	IEA					C	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0009473	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000007	PMID:7719337	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2022-11-05]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000348	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0008665	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0002967	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000268	OMIM:214110	TAS					P	HPO:probinson[2012-05-01]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0001511	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0002104	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000028	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0000347	OMIM:214110	IEA					P	HPO:skoehler[2018-10-08]
OMIM:214110	Peroxisome biogenesis disorder 2A (Zellweger)		HP:0002764	OMIM:214110	IEA					P	HPO:iea[2009-02-17]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0002135	PMID:15908569	PCS					P	HPO:probinson[2013-03-31]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0001298	PMID:15908569	PCS					P	HPO:probinson[2013-03-31]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0002059	PMID:15908569	PCS					P	HPO:probinson[2013-03-31]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0000252	OMIM:610181	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0001332	OMIM:610181	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0003828	OMIM:610181	TAS					M	HPO:skoehler[2015-12-30]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0000007	PMID:15908569	PCS					I	HPO:probinson[2013-01-09]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0100827	OMIM:610181	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0001258	OMIM:610181	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:610181	Aicardi-Goutieres syndrome 2		HP:0009704	PMID:15908569	PCS					P	HPO:probinson[2013-03-31]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0002069	PMID:29100083	PCS	HP:0011463	3/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0002067	OMIM:617836	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0002353	OMIM:617836	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0000750	OMIM:617836	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0002123	PMID:29100083	PCS	HP:0011463	5/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0001332	OMIM:617836	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0004322	OMIM:617836	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0001263	PMID:29100083	PCS	HP:0003593	7/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0002063	OMIM:617836	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0001251	PMID:29100083	PCS		4/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0001290	PMID:29100083	PCS		3/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0011150	PMID:29100083	PCS	HP:0011463	2/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0007099	PMID:29100083	PCS		1/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0003828	OMIM:617836	IEA					M	HPO:skoehler[2018-10-08]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0200134	PMID:29100083	PCS		7/7			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0000006	PMID:29100083	PCS					I	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0001337	PMID:29100083	PCS		6/8			P	HP:probinson[2018-07-07]
OMIM:617836	Developmental delay and seizures with or without movement abnormalities		HP:0001249	OMIM:617836	IEA					P	HPO:skoehler[2018-10-08]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0003510	OMIM:302000	IEA					P	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0000252	OMIM:302000	IEA					P	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0007418	OMIM:302000	IEA					P	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0009381	OMIM:302000	TAS					P	HPO:probinson[2013-04-09]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0001597	OMIM:302000	IEA					P	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0001063	OMIM:302000	IEA					P	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0003819	OMIM:302000	IEA					C	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0000953	OMIM:302000	IEA					P	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0001182	OMIM:302000	TAS					P	HPO:probinson[2013-04-09]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0001417	OMIM:302000	IEA					I	HPO:iea[2009-02-17]
OMIM:302000	Bullous dystrophy, hereditary Macular type		HP:0001249	OMIM:302000	IEA					P	HPO:iea[2009-02-17]
OMIM:613488	Myxoid liposarcoma		HP:0001442	OMIM:613488	IEA					I	HPO:probinson[2013-04-07]
OMIM:613488	Myxoid liposarcoma		HP:0012268	OMIM:613488	TAS					P	HPO:probinson[2013-04-07]
OMIM:206500	Anencephaly		HP:0002323	PMID:28087737	PCS	HP:0003577	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-14]
OMIM:206500	Anencephaly		HP:0003577	PMID:28087737	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2021-07-14]
OMIM:206500	Anencephaly		HP:0000007	PMID:28087737	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-07-14]
OMIM:206500	Anencephaly		HP:0002414	PMID:28087737	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-14]
OMIM:612782	Immunodeficiency 9		HP:0003577	PMID:20004786	PCS		6/6			C	HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0002046	OMIM:612782	TAS					P	HPO:skoehler[2015-06-22]
OMIM:612782	Immunodeficiency 9		HP:0003198	OMIM:612782	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612782	Immunodeficiency 9		HP:0001252	PMID:20004786	PCS		6/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0003391	OMIM:612782	TAS					P	HPO:skoehler[2015-06-22]
OMIM:612782	Immunodeficiency 9		HP:0001508	PMID:20004786	PCS		4/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0002719	PMID:20004786	PCS		5/6			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0000778	PMID:20004786	PCS		3/6			P	HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0001888	PMID:20004786	PCS		0/6			P	HPO:probinson[2024-03-14]
OMIM:612782	Immunodeficiency 9		HP:0003701	OMIM:612782	TAS					P	HPO:skoehler[2015-06-22]
OMIM:612782	Immunodeficiency 9		HP:0001522	PMID:20004786	PCS		4/6			C	HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0004315	PMID:20004786	PCS		0/5			P	HPO:probinson[2024-03-14]
OMIM:612782	Immunodeficiency 9		HP:0002850	PMID:20004786	PCS		1/5			P	HPO:probinson[2024-03-14]
OMIM:612782	Immunodeficiency 9		HP:0001288	OMIM:612782	TAS					P	HPO:skoehler[2015-06-22]
OMIM:612782	Immunodeficiency 9		HP:0020086	PMID:20004786	PCS		1/6			P	HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0001263	PMID:20004786	PCS		2/6			P	HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0011107	OMIM:612782	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612782	Immunodeficiency 9		HP:0010280	OMIM:612782	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612782	Immunodeficiency 9		HP:0000705	PMID:20004786	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0000968	PMID:20004786	PCS		2/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0040089	PMID:20004786	PCS		0/4			P	HPO:probinson[2024-03-14]
OMIM:612782	Immunodeficiency 9		HP:0000007	PMID:20004786	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0001954	OMIM:612782	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612782	Immunodeficiency 9		HP:0002747	OMIM:612782	TAS					P	HPO:skoehler[2015-06-22]
OMIM:612782	Immunodeficiency 9		HP:0002720	PMID:20004786	PCS		0/5			P	HPO:probinson[2024-03-14]
OMIM:612782	Immunodeficiency 9		HP:0002721	PMID:20004786	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-08]
OMIM:612782	Immunodeficiency 9		HP:0002028	PMID:20004786	PCS		3/6			P	HPO:probinson[2023-03-08]
OMIM:620056	Polycystic kidney disease 7		HP:0003774	PMID:35896117	PCS		6/19			P	HPO:probinson[2022-11-25]
OMIM:620056	Polycystic kidney disease 7		HP:0012585	PMID:35896117	PCS		7/17			P	HPO:probinson[2022-11-25]
OMIM:620056	Polycystic kidney disease 7		HP:0032948	PMID:35896117	PCS		1/1			P	HPO:probinson[2022-11-25]
OMIM:620056	Polycystic kidney disease 7		HP:0000083	PMID:35896117	PCS		10/19			P	HPO:probinson[2022-11-25]
OMIM:620056	Polycystic kidney disease 7		HP:0003581	PMID:35896117	PCS		19/19			C	HPO:probinson[2022-11-25]
OMIM:620056	Polycystic kidney disease 7		HP:0005562	PMID:35896117	PCS		16/17			P	HPO:probinson[2022-11-25]
OMIM:620056	Polycystic kidney disease 7		HP:0000822	PMID:35896117	PCS		9/18			P	HPO:probinson[2022-11-25]
OMIM:620056	Polycystic kidney disease 7		HP:0000006	PMID:35896117	PCS					I	HPO:probinson[2022-11-25]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000046	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000486	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001250	OMIM:617822	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0003196	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001290	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0012793	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000518	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000316	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001845	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000238	PMID:25558065	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000476	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001249	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000358	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001188	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000054	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001344	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000496	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001263	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001181	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0010557	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0012385	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000969	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0007033	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001339	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000007	PMID:25558065	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-01-22]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000601	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001698	OMIM:617822	IEA		HP:0040284			P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000369	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0003577	OMIM:617822	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000582	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0002202	PMID:25558065	PCS		1/1			P	HPO:probinson[2023-01-22]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000463	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000540	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0002365	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0002282	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0012725	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000657	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001305	PMID:25558065	PCS		1/1			P	HPO:probinson[2023-01-22]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0002119	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0030084	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000218	OMIM:617822	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000256	OMIM:617822	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001760	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001762	PMID:25558065	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-01-22]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001321	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0005280	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000708	OMIM:617822	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0007370	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0002804	OMIM:617822	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0001357	OMIM:617822	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000465	OMIM:617822	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617822	Alkuraya-Kucinskas syndrome		HP:0000347	PMID:25558065	PCS		1/1			P	HPO:probinson[2023-01-22];HPO:probinson[2023-01-22]
OMIM:608902	Drug metabolism, poor, cyp2d6-relateddrug metabolism, ultrarapid, cyp2d6-related, included		HP:0002664	OMIM:608902	IEA					P	HPO:iea[2009-02-17]
OMIM:608902	Drug metabolism, poor, cyp2d6-relateddrug metabolism, ultrarapid, cyp2d6-related, included		HP:0001939	OMIM:608902	IEA					P	HPO:iea[2009-02-17]
OMIM:608902	Drug metabolism, poor, cyp2d6-relateddrug metabolism, ultrarapid, cyp2d6-related, included		HP:0000007	OMIM:608902	TAS					I	HPO:probinson[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0001265	OMIM:601098	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003401	PMID:19541485	PCS		1/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003621	PMID:19541485	PCS		1/2			C	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0033748	PMID:19541485	PCS		2/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003596	PMID:19541485	PCS		1/2			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003431	PMID:19541485	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0001761	PMID:19541485	PCS		1/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003693	OMIM:601098	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0001271	PMID:19541485	PCS		2/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0002066	PMID:19541485	PCS		2/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003383	OMIM:601098	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0002460	OMIM:601098	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0001251	PMID:19541485	PCS		1/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003481	OMIM:601098	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0003382	OMIM:601098	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0007141	PMID:19541485	PCS		2/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0007230	PMID:19541485	PCS		2/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0002936	OMIM:601098	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0002403	PMID:19541485	PCS		1/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0000762	PMID:19541485	PCS		2/2			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601098	Charcot-Marie-Tooth disease, demyelinating, type 1C		HP:0000006	PMID:12525712	PCS					I	HPO:skoehler[2009-02-17];HPO:probinson[2022-09-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0003202	PMID:25751282	PCS		6/6		HP:0012825	P	HPO:skoehler[2015-04-19];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0003487	PMID:25751282	PCS		6/6			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0001288	PMID:25751282	PCS		6/6			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0034397	PMID:25751282	PCS		2/5			P	HPO:probinson[2022-12-18]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0003581	PMID:25751282	PCS		6/6			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0034399	PMID:25751282	PCS		6/6			P	HPO:probinson[2022-12-18]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0003701	PMID:25751282	PCS		6/6		HP:0012825	P	HPO:skoehler[2015-04-19];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0001258	PMID:25751282	PCS		6/6			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0006886	PMID:25751282	PCS		6/6			P	HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0000006	PMID:25751282	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0003677	PMID:25751282	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-04]
OMIM:616282	Spastic paraplegia 73, autosomal dominant		HP:0001347	PMID:25751282	PCS		6/6			P	HPO:skoehler[2015-04-19];HPO:probinson[2022-11-04]
OMIM:553000	Oncocytoma		HP:0001427	PMID:21555623	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-17]
OMIM:553000	Oncocytoma		HP:0011798	OMIM:553000	TAS					P	HPO:probinson[2021-06-26];HPO:probinson[2021-06-26]
OMIM:620730	Hyperemesis gravidarum, susceptibility to		HP:0012188	PMID:38092039	PCS					H	HPO:probinson[2024-06-29]
OMIM:620730	Hyperemesis gravidarum, susceptibility to		HP:0000006	PMID:38092039	PCS					I	HPO:probinson[2024-06-29]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0002153	PMID:22266938	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2023-01-28]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0008242	PMID:22266938	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2023-01-28]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0004918	PMID:22266938	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2023-01-28]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0011462	PMID:22266938	PCS					C	HPO:probinson[2023-01-28]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0000822	PMID:22266938	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0000007	PMID:22266938	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0011423	PMID:22266938	PCS					P	HPO:skoehler[2012-11-21];HPO:probinson[2023-01-28]
OMIM:614495	Pseudohypoaldosteronism, type IID		HP:0000006	PMID:22266938	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-28]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0001100	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0002211	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0000407	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0001053	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0002251	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0000635	OMIM:613265	IEA					P	HPO:skoehler[2010-06-20]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0000007	OMIM:613265	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0002216	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0002227	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0000006	OMIM:613265	IEA					I	HPO:skoehler[2010-06-19]
OMIM:613265	Waardenburg syndrome, type 4B		HP:0002226	OMIM:613265	IEA					P	HPO:skoehler[2010-06-19]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0003785	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0008936	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0000750	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0001300	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0002375	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0000298	OMIM:605407	TAS					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0002066	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0002451	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0002063	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0003593	OMIM:605407	IEA					C	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0001270	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0002071	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0003828	OMIM:605407	TAS					M	HPO:skoehler[2013-03-15]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0000508	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0000007	OMIM:605407	IEA					I	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0002548	OMIM:605407	TAS					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0001337	OMIM:605407	IEA					P	HPO:iea[2018-03-07]
OMIM:605407	Segawa syndrome, autosomal recessive		HP:0001336	PMID:8817341	PCS		HP:0040283			P	HPO:skoehler[2018-03-07]
OMIM:620877	Deafness, autosomal recessive 125		HP:0003577	PMID:33964205	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620877	Deafness, autosomal recessive 125		HP:0000750	PMID:33964205	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620877	Deafness, autosomal recessive 125		HP:0001751	PMID:33964205	PCS		0/3			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620877	Deafness, autosomal recessive 125		HP:0000407	PMID:33964205	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620877	Deafness, autosomal recessive 125		HP:0011463	PMID:33964205	PCS		2/4			C	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620877	Deafness, autosomal recessive 125		HP:0001999	PMID:33964205	PCS		0/4			P	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:620877	Deafness, autosomal recessive 125		HP:0000007	PMID:33964205	PCS					I	ORCID:0000-0002-0736-9199[2024-12-15]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0004322	PMID:30014507	PCS		2/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001252	PMID:30014507	PCS		3/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0003593	PMID:30014507	PCS		9/9			C	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001270	PMID:30014507	PCS		7/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0012704	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001629	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000337	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000414	PMID:30014507	PCS		2/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000637	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000219	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001643	PMID:30014507	PCS		2/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001249	PMID:30014507	PCS		6/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000677	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0006956	PMID:30014507	PCS		1/9		HP:0012833	P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000750	PMID:30014507	PCS		9/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000276	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001263	PMID:30014507	PCS		9/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0100632	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0007010	PMID:30014507	PCS		2/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000767	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000601	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001357	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0002007	PMID:30014507	PCS		2/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000047	PMID:30014507	PCS		2/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0001631	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000006	PMID:30014507	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-25]
OMIM:618330	Global developmental delay with or without impaired intellectual development		HP:0000369	PMID:30014507	PCS		1/9			P	HPO:probinson[2023-03-25]
OMIM:608645	Deafness, autosomal dominant 31		HP:0040113	OMIM:608645	TAS					P	HPO:skoehler[2015-09-11]
OMIM:608645	Deafness, autosomal dominant 31		HP:0000006	OMIM:608645	TAS					I	HPO:skoehler[2015-09-11]
OMIM:618456	Deafness, autosomal recessive 114		HP:0000407	PMID:30610177	PCS				HP:0012828	P	HPO:nvasilevsky[2019-09-11]
OMIM:618456	Deafness, autosomal recessive 114		HP:0000007	OMIM:618456	IEA					I	HPO:skoehler[2019-09-07]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0002850	PMID:27016798	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0005357	PMID:27016798	PCS					P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0032140	PMID:27016798	PCS		1/1			P	HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0030388	PMID:27016798	PCS		2/3			P	HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0005387	PMID:27016798	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0011108	PMID:27016798	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0000006	PMID:27016798	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0003765	PMID:27016798	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0002720	PMID:27016798	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0002028	PMID:27016798	PCS		1/3			P	HPO:probinson[2021-05-09]
OMIM:617765	Immunodeficiency, common variable, 14		HP:0004315	PMID:27016798	PCS		3/3			P	HPO:probinson[2021-05-09]
OMIM:273000	Teeth, fused		HP:0000164	OMIM:273000	IEA					P	HPO:iea[2009-02-17]
OMIM:273000	Teeth, fused		HP:0000007	OMIM:273000	IEA					I	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0002015	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0001310	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0002354	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0001272	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0001260	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0002066	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0006938	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0004373	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0002073	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0000639	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0000716	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0003829	OMIM:605361	IEA					I	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0000317	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0001268	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0007018	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0000006	OMIM:605361	IEA					I	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0003677	OMIM:605361	IEA					C	HPO:iea[2009-02-17]
OMIM:605361	Spinocerebellar ataxia 14		HP:0001347	OMIM:605361	IEA					P	HPO:iea[2009-02-17]
OMIM:605375	Epilepsy, nocturnal frontal lobe, 3		HP:0001250	PMID:11104662	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2020-07-20]
OMIM:605375	Epilepsy, nocturnal frontal lobe, 3		HP:0000006	PMID:11104662	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2020-07-20]
OMIM:189100	Toe, misshapen		HP:0000924	OMIM:189100	IEA					P	HPO:iea[2009-02-17]
OMIM:189100	Toe, misshapen		HP:0000006	OMIM:189100	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:614278	Platelet-Activating factor acetylhydrolase deficiency		HP:0040175	PMID:8675689	PCS					P	HPO:skoehler[2015-08-24];HPO:probinson[2022-04-10]
OMIM:614278	Platelet-Activating factor acetylhydrolase deficiency		HP:0040178	PMID:10194471	PCS					P	HPO:skoehler[2015-08-24];HPO:probinson[2022-04-10]
OMIM:614278	Platelet-Activating factor acetylhydrolase deficiency		HP:0000007	PMID:8675689	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-04-10]
OMIM:613517	Microphthalmia, isolated 6		HP:0008052	OMIM:613517	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613517	Microphthalmia, isolated 6		HP:0007906	PMID:21850159	PCS		3/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-02]
OMIM:613517	Microphthalmia, isolated 6		HP:0000482	OMIM:613517	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613517	Microphthalmia, isolated 6		HP:0008499	PMID:21850159	PCS		9/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-04-02]
OMIM:613517	Microphthalmia, isolated 6		HP:0000646	PMID:21850159	PCS		2/9			P	HPO:probinson[2023-04-02]
OMIM:613517	Microphthalmia, isolated 6		HP:0000007	PMID:21397065	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-02]
OMIM:613517	Microphthalmia, isolated 6		HP:0000568	PMID:21850159	PCS		9/9			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-04-02]
OMIM:613517	Microphthalmia, isolated 6		HP:0030823	OMIM:613517	TAS					P	HPO:skoehler[2017-07-13]
OMIM:140300	Hashimoto thyroiditis		HP:0030057	OMIM:140300	TAS					P	HPO:probinson[2015-02-15]
OMIM:140300	Hashimoto thyroiditis		HP:0000872	OMIM:140300	TAS					P	HPO:probinson[2009-02-17]
OMIM:140300	Hashimoto thyroiditis		HP:0000006	OMIM:140300	TAS					I	HPO:probinson[2009-02-17]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0002521	PMID:29069600	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0002376	OMIM:617771	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0002123	OMIM:617771	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0002079	OMIM:617771	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0001250	PMID:29069600	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0025401	PMID:29069600	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0001263	OMIM:617771	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0001252	PMID:29069600	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0003593	OMIM:617771	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0012736	PMID:29069600	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0033725	PMID:29069600	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0011097	PMID:29069600	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0007270	OMIM:617771	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0034295	PMID:29069600	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0032792	PMID:29069600	PCS		1/1			P	HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0200134	PMID:29069600	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0000006	PMID:29069600	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-08]
OMIM:617771	Developmental and epileptic encephalopathy 57		HP:0003623	PMID:29069600	PCS		1/1			C	HPO:probinson[2023-03-08]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001792	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0005214	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000486	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002024	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0004322	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002860	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001371	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000482	OMIM:601675	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0003196	PMID:9758621	PCS					P	HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001097	OMIM:601675	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0003593	PMID:9758621	PCS		11/11			C	HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0045055	OMIM:601675	TAS					P	HP:probinson[2019-04-19]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0008070	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001808	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000518	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000958	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000639	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002719	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0007485	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000613	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001009	OMIM:601675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0009886	PMID:9758621	PCS		11/11			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000411	OMIM:601675	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001522	PMID:9758621	PCS		4/11			C	HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000135	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000278	PMID:9758621;OMIM:601675	PCS		20/20			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001249	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0004315	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002213	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000252	PMID:9758621	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000992	PMID:9758621	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000750	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002299	OMIM:601675	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002099	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002671	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001480	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001518	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0034354	PMID:9758621	PCS		11/11			P	HPO:probinson[2022-09-05]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000007	PMID:9758621	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0001019	PMID:9758621	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000568	OMIM:601675	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000207	OMIM:601675	IEA					P	HPO:skoehler[2019-09-07]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0007479	OMIM:601675	IEA					P	HPO:iea[2009-02-17]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0008404	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000400	PMID:9758621	PCS					P	HPO:probinson[2022-03-26]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0002028	OMIM:601675	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0000962	OMIM:601675	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601675	Trichothiodystrophy 1, photosensitive		HP:0003777	PMID:9758621	PCS		11/11			P	HPO:probinson[2022-03-26]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0002540	PMID:30503518	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0000486	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0002188	PMID:30503518	PCS		1/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0001272	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0001250	PMID:30503518	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0001252	PMID:30503518	PCS		2/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0001274	PMID:30503518	PCS		1/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0002020	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0000639	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0100704	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0011463	PMID:30503518	PCS		2/2			C	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0006970	PMID:30503518	PCS		1/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0001622	PMID:30503518	PCS		1/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0011968	PMID:30503518	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0001263	PMID:30503518	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0030948	PMID:30503518	PCS		1/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0002093	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0034392	PMID:30503518	PCS		2/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0034353	PMID:30503518	PCS		1/2			P	HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0000007	PMID:30503518	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0200134	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0000648	PMID:30503518	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0000505	PMID:30503518	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-08]
OMIM:618324	Congenital disorder of glycosylation with defective fucosylation 2		HP:0002205	PMID:30503518	PCS		1/2			P	HPO:probinson[2022-10-08]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0001265	PMID:26991897	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0003596	PMID:26991897	PCS		8/10			C	HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0001284	OMIM:617017	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0009053	PMID:26991897	PCS		10/10			P	HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0007141	PMID:26991897	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0000726	PMID:26991897	PCS		0/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0009027	OMIM:617017	TAS					P	HPO:skoehler[2017-07-13]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0000007	PMID:26991897	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0002936	PMID:26991897	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0002317	PMID:26991897	PCS		10/10			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0025710	PMID:26991897	PCS		2/10			C	HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0000006	OMIM:617017	TAS					I	HPO:skoehler[2017-07-13]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0003677	PMID:26991897	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-07]
OMIM:617017	Charcot-Marie-Tooth disease, axonal, type 2T		HP:0008944	PMID:26991897	PCS		10/10			P	HPO:probinson[2023-02-07]
OMIM:161480	Nasal bones, absence of		HP:0000271	OMIM:161480	IEA					P	HPO:iea[2009-02-17]
OMIM:161480	Nasal bones, absence of		HP:0002000	OMIM:161480	TAS					P	HPO:skoehler[2017-07-13]
OMIM:161480	Nasal bones, absence of		HP:0009933	OMIM:161480	TAS					P	HPO:skoehler[2017-07-13]
OMIM:161480	Nasal bones, absence of		HP:0000006	OMIM:161480	IEA					I	HPO:iea[2009-02-17]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0002421	PMID:11782989	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0002015	PMID:11782989	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0003324	PMID:11782989	PCS		1/1		HP:0012828	P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0003676	PMID:11782989	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0003388	PMID:11782989	PCS		1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0001252	PMID:11782989	PCS	HP:0003623	1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0003593	PMID:11782989	PCS		1/1			C	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0002093	PMID:11782989	PCS		1/1		HP:0025303	P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0000508	PMID:11782989	PCS	HP:0003593	1/1			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0025336	PMID:11782989	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0002505	PMID:11782989	PCS	HP:0003621	1/1			P	HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0000006	PMID:11782989	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0003402	PMID:11782989	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0003403	PMID:11782989	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:616321	Myasthenic syndrome, congenital, 3A, slow-channel		HP:0003436	PMID:11782989	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0000252	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0011924	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0001250	PMID:32488845	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0001263	PMID:27356879;PMID:32488845	PCS		2/2			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0002151	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0001252	PMID:32488845	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0003593	PMID:27356879;PMID:32488845	IEA		2/2			C	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0011923	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04];HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0012762	PMID:32488845	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0000639	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0001508	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0030890	PMID:32488845	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0000007	PMID:27356879	PCS		1/1			I	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0008347	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0001324	PMID:27356879;PMID:32488845	PCS		2/2			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0000544	PMID:27356879	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:619012	Combined oxidative phosphorylation deficiency 48		HP:0003128	PMID:32488845	PCS		1/1			P	HPO:probinson[2022-03-04]
OMIM:601885	Cataract, zonular pulverulent 3		HP:0010920	OMIM:601885	IEA					P	HPO:skoehler[2013-01-09]
OMIM:601885	Cataract, zonular pulverulent 3		HP:0000006	OMIM:601885	IEA					I	HPO:skoehler[2013-01-09]
OMIM:188550	Thyroid cancer, nonmedullary, 1		HP:0002895	OMIM:188550	TAS					P	HPO:probinson[2009-02-17]
OMIM:188550	Thyroid cancer, nonmedullary, 1		HP:0040198	OMIM:188550	TAS					P	HPO:skoehler[2015-12-30]
OMIM:188550	Thyroid cancer, nonmedullary, 1		HP:0000006	OMIM:188550	TAS					I	HPO:probinson[2009-02-17]
OMIM:188550	Thyroid cancer, nonmedullary, 1		HP:0000853	OMIM:188550	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0002069	PMID:19196676	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0000473	PMID:19196676	PCS		1/3			P	HPO:skoehler[2013-11-28];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0000252	PMID:21237447	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0002353	OMIM:612621	TAS					P	HPO:skoehler[2014-05-04]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0002342	PMID:19196676;PMID:21237447	PCS		6/6			P	HPO:probinson[2022-06-18];HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0002463	PMID:21237447	PCS					P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0000486	PMID:19196676	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0002376	OMIM:612621	TAS					P	HPO:skoehler[2013-10-06]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0001250	PMID:21237447	PCS		4/6			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-18];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0001263	PMID:19196676	PCS		3/3			P	HPO:skoehler[2014-04-04];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0001252	PMID:19196676	PCS		3/3			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0003593	PMID:19196676	PCS		3/3			C	HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0001270	PMID:19196676	PCS		3/3			P	HPO:probinson[2013-04-06];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0012444	PMID:21237447	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0011150	PMID:19196676	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0000729	PMID:21237447	PCS		1/3			P	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0200134	PMID:19196676	PCS					P	HPO:skoehler[2013-10-06];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0002307	PMID:19196676	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0000006	PMID:19196676	PCS					I	HPO:probinson[2013-04-06];HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0005988	PMID:19196676	PCS		1/3			P	HPO:probinson[2022-06-18]
OMIM:612621	Intellectual developmental disorder, autosomal dominant 5		HP:0001249	OMIM:612621	TAS					P	HPO:probinson[2013-04-06]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0001034	PMID:666331	PCS					P	HPO:probinson[2009-02-17]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0007505	PMID:21368769	PCS					P	HPO:probinson[2009-02-17]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0001045	OMIM:145250	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0001003	PMID:21368769	PCS					P	HPO:probinson[2017-05-29]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0000957	PMID:21368769	PCS					P	HPO:skoehler[2015-04-05]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0001053	PMID:21368769	PCS					P	HPO:skoehler[2015-04-05]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0003593	PMID:19375057	PCS					C	HPO:probinson[2017-05-29]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0000006	PMID:21368769	PCS					I	HPO:probinson[2009-02-17]
OMIM:145250	Hyperpigmentation, familial progressive		HP:0000962	OMIM:145250	TAS					P	HPO:skoehler[2009-02-17]
OMIM:305800	Membranoproliferative glomerulonephritis, X-linked		HP:0001693	OMIM:305800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:305800	Membranoproliferative glomerulonephritis, X-linked		HP:0000793	OMIM:305800	IEA					P	HPO:iea[2009-02-17]
OMIM:305800	Membranoproliferative glomerulonephritis, X-linked		HP:0001939	OMIM:305800	IEA					P	HPO:iea[2009-02-17]
OMIM:305800	Membranoproliferative glomerulonephritis, X-linked		HP:0009125	OMIM:305800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:614250	Narcolepsy 7		HP:0002870	PMID:21907016	PCS		3/6			P	HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0002519	PMID:21907016	PCS		3/6			P	HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0011462	PMID:21907016	PCS		6/6			C	HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0001262	PMID:21907016	PCS	HP:0011462	6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0025233	PMID:21907016	PCS		3/6			P	HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0002524	PMID:21907016	PCS	HP:0011462	6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0030050	PMID:21907016	PCS					P	HPO:skoehler[2015-01-20];HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0005978	PMID:21907016	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0001513	PMID:21907016	PCS		5/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
OMIM:614250	Narcolepsy 7		HP:0000006	PMID:21907016	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-03]
DECIPHER:32	22q11 duplication syndrome		HP:0000506	DECIPHER:32	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:32	22q11 duplication syndrome		HP:0001249	DECIPHER:32	IEA					P	HPO:skoehler[2013-05-29]
DECIPHER:32	22q11 duplication syndrome		HP:0001611	DECIPHER:32	IEA					P	HPO:skoehler[2013-05-29]
OMIM:619774	Immunodeficiency 96		HP:0002850	PMID:30395541	PCS		5/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0002783	PMID:1581963	PCS		1/1			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0003593	PMID:30395541	IEA		2/5			C	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0001270	PMID:1581963	PCS		1/1			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0031379	PMID:1581963	PCS		1/1			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0002719	PMID:30395541	PCS		5/5			P	HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0011463	PMID:30395541	PCS		3/5			C	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0500270	PMID:30395541	PCS		4/4			P	HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0000007	PMID:1581963	PCS					I	HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0000524	PMID:1581963	PCS		1/1			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0000403	PMID:1581963	PCS		1/1			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0000964	PMID:30395541	PCS		1/5			P	HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0005518	PMID:30395541	PCS		5/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0001510	PMID:1581963	PCS		1/1			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0000003	PMID:30395541	PCS		2/5			P	HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0002720	PMID:30395541;PMID:1581963	PCS		6/6			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0001249	PMID:30395541	PCS		0/5			P	HPO:probinson[2022-05-29]
OMIM:619774	Immunodeficiency 96		HP:0004315	PMID:30395541;PMID:1581963	PCS		6/6			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:617981	Erythrocytosis 7		HP:0001900	PMID:15921161	PCS					P	HPO:probinson[2021-02-19]
OMIM:617981	Erythrocytosis 7		HP:0001899	PMID:15921161	PCS					P	HPO:probinson[2021-02-19]
OMIM:617981	Erythrocytosis 7		HP:0001901	PMID:15921161	PCS					P	HPO:probinson[2021-02-19]
OMIM:617981	Erythrocytosis 7		HP:0000006	PMID:15921161	PCS					I	HPO:probinson[2021-02-19];HPO:probinson[2021-02-19]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0002465	OMIM:300978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0004322	OMIM:300978	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000160	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0003593	PMID:25735484	PCS		4/4			C	HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001290	OMIM:300978	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0100962	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000718	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000316	PMID:25735484	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000635	PMID:25735484	PCS		1/3			P	HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0008734	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001763	OMIM:300978	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001249	PMID:25735484	PCS		4/4	MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000494	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000252	OMIM:300978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000054	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0011968	PMID:25735484	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001263	OMIM:300978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001419	PMID:25735484	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000729	PMID:25735484	PCS		3/4			P	HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000448	OMIM:300978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000601	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000444	PMID:25735484	PCS		1/3			P	HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000047	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001257	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001337	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000687	PMID:25735484	PCS		1/3			P	HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000220	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001792	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0002089	OMIM:300978	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001156	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000739	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000337	PMID:25735484	PCS		3/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001627	OMIM:300978	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0002714	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000776	OMIM:300978	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001347	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000275	OMIM:300978	IEA					P	HPO:skoehler[2019-09-07]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0002136	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0002015	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0002213	PMID:25735484	PCS		2/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000750	PMID:25735484	PCS		3/3			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000431	PMID:25735484	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000272	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0011304	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000708	OMIM:300978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000426	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0100716	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001510	OMIM:300978	IEA					P	HPO:skoehler[2019-02-22]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0001598	PMID:25735484	PCS		1/3			P	HPO:probinson[2022-10-18]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000028	OMIM:300978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300978	Tonne-Kalscheuer syndrome		HP:0000347	OMIM:300978	TAS					P	HPO:skoehler[2017-07-13]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002322	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0010628	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0008209	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003676	OMIM:157640	IEA					C	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002067	OMIM:157640	IEA		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003596	PMID:15534189	PCS		1/2			C	HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002066	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002063	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0001350	PMID:15534189	PCS		1/2			P	HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003690	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003390	OMIM:157640	IEA		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000518	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000716	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000815	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0025710	PMID:15534189	PCS		1/2			C	HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003548	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003688	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003546	OMIM:157640	IEA		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002578	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003689	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003722	PMID:15534189	PCS		1/2			P	HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0001265	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003323	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003202	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0007824	PMID:15534189	PCS		1/2			P	HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002015	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002378	PMID:15534189	PCS		1/2			P	HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000651	PMID:15534189	PCS		1/2			P	HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0006858	OMIM:157640	TAS					P	HPO:probinson[2012-04-28]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0001300	OMIM:157640	IEA		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003200	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0001761	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003201	OMIM:157640	IEA					P	HPO:skoehler[2018-10-08]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000590	OMIM:157640	IEA					P	HPO:skoehler[2010-06-18]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0001260	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003581	OMIM:157640	IEA					C	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002151	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000869	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000407	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000508	OMIM:157640	IEA		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000029	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0002548	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0006886	OMIM:157640	TAS		1/2			P	HPO:probinson[2012-04-28];HPO:probinson[2022-11-27]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003713	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000006	OMIM:157640	IEA					I	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003458	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0003557	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:157640	Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1		HP:0000786	OMIM:157640	IEA					P	HPO:iea[2009-02-17]
OMIM:600231	Palmoplantar keratoderma, Bothnian type		HP:0011463	PMID:23830519	PCS					C	HPO:probinson[2021-05-02]
OMIM:600231	Palmoplantar keratoderma, Bothnian type		HP:0007447	PMID:23830519	PCS					P	HPO:probinson[2021-05-02]
OMIM:600231	Palmoplantar keratoderma, Bothnian type		HP:0000006	PMID:23830519	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-05-02]
OMIM:606640	Amyotrophic lateral sclerosis 3		HP:0001272	PMID:11706389	PCS		0/20			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-10]
OMIM:606640	Amyotrophic lateral sclerosis 3		HP:0002483	PMID:11706389	PCS		20/20			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-10]
OMIM:606640	Amyotrophic lateral sclerosis 3		HP:0000726	PMID:11706389	PCS		0/20			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-10]
OMIM:606640	Amyotrophic lateral sclerosis 3		HP:0007340	PMID:11706389	PCS		20/20			P	HPO:probinson[2017-06-25];HPO:probinson[2024-03-10]
OMIM:606640	Amyotrophic lateral sclerosis 3		HP:0003581	PMID:11706389	PCS		20/20			C	HPO:probinson[2022-06-16];HPO:probinson[2024-03-10]
OMIM:606640	Amyotrophic lateral sclerosis 3		HP:0000006	PMID:11706389	PCS					I	HPO:probinson[2017-06-25]
OMIM:248900	Mast syndrome		HP:0001276	PMID:14564668	PCS		14/14			P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0002186	OMIM:248900	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:248900	Mast syndrome		HP:0001272	PMID:14564668	PCS		3/3			P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0030891	PMID:14564668	PCS		1/1			P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0001270	PMID:14564668	PCS		10/11			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0033725	PMID:14564668	PCS		3/3			P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0012672	PMID:14564668	PCS	HP:0003581				P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0011463	PMID:14564668	PCS					C	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0007340	OMIM:248900	TAS					P	HPO:skoehler[2014-10-06]
OMIM:248900	Mast syndrome		HP:0002313	OMIM:248900	IEA					P	HPO:iea[2009-02-17]
OMIM:248900	Mast syndrome		HP:0001347	PMID:14564668	PCS		14/14			P	HPO:skoehler[2014-10-06]
OMIM:248900	Mast syndrome		HP:0002311	PMID:14564668	PCS					P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0002476	PMID:14564668	PCS		9/13			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0002059	PMID:14564668	PCS		3/3			P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0002015	PMID:14564668	PCS		9/14			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0003487	PMID:14564668	PCS		14/14			P	HPO:skoehler[2014-10-06]
OMIM:248900	Mast syndrome		HP:0001288	PMID:14564668	PCS		14/14			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0001260	PMID:14564668	PCS		14/14			P	HPO:skoehler[2014-10-06]
OMIM:248900	Mast syndrome		HP:0002075	PMID:14564668	PCS					P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0000726	PMID:14564668	PCS		14/14			P	HPO:skoehler[2010-06-20]
OMIM:248900	Mast syndrome		HP:0033683	PMID:14564668	PCS		7/12			P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0009830	OMIM:248900	TAS		HP:0040283			P	HPO:skoehler[2014-10-06]
OMIM:248900	Mast syndrome		HP:0000007	PMID:14564668	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0001258	OMIM:248900	TAS					P	HPO:skoehler[2014-10-06]
OMIM:248900	Mast syndrome		HP:0002305	PMID:14564668	PCS		3/14			P	HPO:probinson[2023-02-20]
OMIM:248900	Mast syndrome		HP:0003677	PMID:14564668	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-02-20]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0000252	OMIM:616335	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0003577	OMIM:616335	TAS					C	HPO:skoehler[2015-12-30]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0000639	OMIM:616335	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0001263	OMIM:616335	TAS				HP:0012825	P	HPO:skoehler[2015-06-22]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0001999	OMIM:616335	TAS		HP:0040283			P	HPO:skoehler[2015-06-22]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0000568	OMIM:616335	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0007663	OMIM:616335	TAS					P	HPO:skoehler[2015-07-26]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0000007	OMIM:616335	TAS					I	HPO:skoehler[2015-12-30]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0000505	OMIM:616335	TAS					P	HPO:skoehler[2015-06-22]
OMIM:616335	Microcephaly and chorioretinopathy, autosomal recessive, 3		HP:0007731	PMID:25817018	PCS					P	HPO:skoehler[2015-07-19]
OMIM:620687	Moyamoya disease 7		HP:0012495	PMID:37253099	PCS					P	HPO:probinson[2024-04-28];HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0100546	PMID:37253099	PCS					P	HPO:probinson[2024-04-28];HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0001297	PMID:37253099	PCS					P	HPO:probinson[2024-04-28];HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0002076	PMID:37253099	PCS					P	HPO:probinson[2024-04-28];HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0011463	PMID:37253099	PCS					C	HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0003581	PMID:37253099	PCS					C	HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0000007	PMID:37253099	PCS					I	HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0001269	PMID:37253099	PCS					P	HPO:probinson[2024-04-28];HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0002326	PMID:37253099	PCS					P	HPO:probinson[2024-04-28];HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0002315	PMID:37253099	PCS					P	HPO:probinson[2024-04-28];HPO:probinson[2024-04-28]
OMIM:620687	Moyamoya disease 7		HP:0000006	PMID:37253099	PCS					I	HPO:probinson[2024-04-28]
OMIM:272450	Syndesmodysplasic dwarfism		HP:0003510	OMIM:272450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272450	Syndesmodysplasic dwarfism		HP:0001387	OMIM:272450	IEA					P	HPO:skoehler[2010-06-20]
OMIM:272450	Syndesmodysplasic dwarfism		HP:0000007	OMIM:272450	IEA					I	HPO:iea[2009-02-17]
OMIM:243100	Internal carotid arteries, hypoplasia of		HP:0000726	OMIM:243100	IEA					P	HPO:iea[2009-02-17]
OMIM:243100	Internal carotid arteries, hypoplasia of		HP:0000007	OMIM:243100	IEA					I	HPO:iea[2009-02-17]
OMIM:243100	Internal carotid arteries, hypoplasia of		HP:0002637	OMIM:243100	IEA					P	HPO:iea[2009-02-17]
OMIM:243100	Internal carotid arteries, hypoplasia of		HP:0005290	OMIM:243100	IEA					P	HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0001254	OMIM:307030	TAS					P	HPO:skoehler[2012-11-20]
OMIM:307030	Glycerol kinase deficiency		HP:0000486	OMIM:307030	TAS					P	HPO:skoehler[2014-01-28]
OMIM:307030	Glycerol kinase deficiency		HP:0001993	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:0004322	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:0003198	OMIM:307030	IEA					P	HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0001250	PMID:8651297	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0000939	OMIM:307030	IEA					P	HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0007185	OMIM:307030	IEA					P	HPO:skoehler[2018-10-08]
OMIM:307030	Glycerol kinase deficiency		HP:0011463	PMID:8651297	PCS		2/4			C	HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0000316	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:0001943	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:0002714	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:0002018	PMID:6299616	PCS		1/1			P	HPO:probinson[2024-01-06];HPO:probinson[2024-01-06]
OMIM:307030	Glycerol kinase deficiency		HP:0002756	OMIM:307030	IEA					P	HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0001942	PMID:6299616	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-06]
OMIM:307030	Glycerol kinase deficiency		HP:0001249	PMID:8651297	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0003326	PMID:6299616	PCS		1/1			P	HPO:probinson[2024-01-06];HPO:probinson[2024-01-06]
OMIM:307030	Glycerol kinase deficiency		HP:0003621	PMID:8651297	PCS		1/4			C	HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0002155	OMIM:307030	TAS					P	HPO:skoehler[2012-11-20]
OMIM:307030	Glycerol kinase deficiency		HP:0002013	PMID:6299616	PCS		1/1			P	HPO:probinson[2024-01-06];HPO:probinson[2024-01-06]
OMIM:307030	Glycerol kinase deficiency		HP:0002572	OMIM:307030	IEA					P	HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0001263	PMID:8651297;OMIM:307030	PCS		12/14			P	HPO:skoehler[2019-02-22];HPO:skoehler[2012-10-17];HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0003581	PMID:8651297	PCS		1/4			C	HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0002151	PMID:6299616	PCS		1/1			P	HPO:probinson[2024-01-06];HPO:probinson[2024-01-06]
OMIM:307030	Glycerol kinase deficiency		HP:0003560	OMIM:307030	TAS					P	HPO:skoehler[2012-11-20]
OMIM:307030	Glycerol kinase deficiency		HP:0040301	PMID:8651297	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0008182	OMIM:307030	IEA					P	HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0006280	PMID:8651297	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:307030	Glycerol kinase deficiency		HP:0040302	PMID:8651297;PMID:6299616	PCS		5/5			P	HPO:probinson[2023-06-09];HPO:probinson[2024-01-06];HPO:probinson[2024-01-06]
OMIM:307030	Glycerol kinase deficiency		HP:0001419	OMIM:307030	TAS					I	HPO:skoehler[2013-06-04]
OMIM:307030	Glycerol kinase deficiency		HP:0001518	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:4000211	PMID:6299616	PCS		1/1			P	HPO:probinson[2024-01-06];HPO:probinson[2024-01-06]
OMIM:307030	Glycerol kinase deficiency		HP:0000846	OMIM:307030	TAS		20/20			P	HPO:skoehler[2012-11-20];HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0002007	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:0001510	OMIM:307030	IEA					P	HPO:iea[2009-02-17]
OMIM:307030	Glycerol kinase deficiency		HP:0000369	OMIM:307030	TAS					P	HPO:skoehler[2012-10-17]
OMIM:307030	Glycerol kinase deficiency		HP:0000028	OMIM:307030	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:307030	Glycerol kinase deficiency		HP:0001259	OMIM:307030	IEA					P	HPO:skoehler[2010-06-20]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0002960	PMID:31040184	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0002014	PMID:31040184	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0000010	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0006527	PMID:31040184	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0001890	PMID:31040184	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0002240	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0003593	PMID:31040184	PCS		2/2			C	HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0032247	PMID:31040184	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0008064	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0001508	PMID:31040184	PCS		2/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0033222	PMID:31040184	PCS		1/2			P	HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0000007	PMID:31040184	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0001558	OMIM:618495	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0002716	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0000403	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0002205	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0001744	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0003237	PMID:31040184	PCS		2/2			P	HPO:probinson[2022-09-06]
OMIM:618495	Immunodeficiency 63 with lymphoproliferation and autoimmunity		HP:0002721	OMIM:618495	IEA					P	HPO:skoehler[2019-09-07]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0001034	PMID:28504826	PCS		1/1			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0001100	PMID:35543077	PCS		4/6			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0003577	PMID:28504826	PCS		1/1			C	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0002211	PMID:35543077	PCS		3/6			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0001010	PMID:35543077;PMID:28504826	PCS		7/7			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0000957	PMID:28504826	PCS		1/1			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0011364	PMID:35543077;PMID:28504826	PCS		3/7			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0000506	PMID:28504826	PCS		1/1			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0000407	PMID:35543077	PCS		5/6			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0000635	PMID:28504826	PCS		1/1			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0000007	PMID:28504826	PCS					I	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0002216	PMID:35543077	PCS		2/6			P	HPO:probinson[2022-08-26]
OMIM:619947	Waardenburg syndrome, type 2F		HP:0008527	PMID:28504826	PCS		1/1			P	HPO:probinson[2022-08-26]
OMIM:618481	Deafness, autosomal recessive 99		HP:0003577	PMID:25331638	PCS		2/2			C	HPO:probinson[2024-03-15]
OMIM:618481	Deafness, autosomal recessive 99		HP:0001751	PMID:25331638	PCS		2/2			P	HPO:probinson[2019-07-06];HPO:probinson[2024-03-15]
OMIM:618481	Deafness, autosomal recessive 99		HP:0000407	PMID:25331638	PCS		2/2		HP:0012829	P	HPO:probinson[2019-07-06];HPO:probinson[2024-03-15]
OMIM:618481	Deafness, autosomal recessive 99		HP:0000007	PMID:25331638	PCS					I	HPO:probinson[2019-07-06];HPO:probinson[2019-07-06]
OMIM:123880	Cystic angiomatosis of bone, diffuse		HP:0000924	OMIM:123880	IEA					P	HPO:iea[2009-02-17]
OMIM:123880	Cystic angiomatosis of bone, diffuse		HP:0002833	OMIM:123880	IEA					P	HPO:skoehler[2015-01-27]
OMIM:123880	Cystic angiomatosis of bone, diffuse		HP:0000006	OMIM:123880	IEA					I	HPO:iea[2009-02-17]
OMIM:174700	Polydactyly, preaxial IV		HP:0011939	OMIM:174700	TAS					P	HPO:probinson[2024-07-22]
OMIM:174700	Polydactyly, preaxial IV		HP:0005688	OMIM:174700	TAS					P	HPO:probinson[2009-02-17]
OMIM:174700	Polydactyly, preaxial IV		HP:0003577	PMID:10441570	PCS		40/40			C	HPO:probinson[2022-12-20]
OMIM:174700	Polydactyly, preaxial IV		HP:0100258	PMID:10441570	PCS		40/40			P	HPO:probinson[2009-02-17];HPO:probinson[2022-12-20]
OMIM:174700	Polydactyly, preaxial IV		HP:0009942	OMIM:174700	IEA					P	HPO:skoehler[2019-09-07]
OMIM:174700	Polydactyly, preaxial IV		HP:0010713	OMIM:174700	TAS					P	HPO:probinson[2009-02-17]
OMIM:174700	Polydactyly, preaxial IV		HP:0000006	PMID:10441570	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-12-20]
OMIM:139600	Hairy elbows		HP:0004322	PMID:139600	PCS		75%			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-04]
OMIM:139600	Hairy elbows		HP:0004780	PMID:139600	IEA					P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-04]
OMIM:139600	Hairy elbows		HP:0001999	PMID:14791960	PCS		25%			P	HPO:lccarmody[2018-10-04]
OMIM:139600	Hairy elbows		HP:0000006	OMIM:139600	TAS		20/20			I	HPO:skoehler[2019-02-22];HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0008936	PMID:24399846	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0003577	PMID:24399846	PCS		4/4			C	HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0011968	PMID:24399846	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0010818	PMID:24399846	PCS		4/4			P	HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0001290	PMID:24399846	PCS	HP:0003577	4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0012736	PMID:24399846	PCS		4/4			P	HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0012444	PMID:24399846	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0011182	PMID:24399846	PCS		4/4			P	HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0002509	PMID:24399846	PCS		4/4			P	HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0031165	PMID:24399846	PCS		4/4			P	HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0000007	PMID:24399846	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0001558	PMID:24399846	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-18]
OMIM:615833	Epileptic encephalopathy, early infantile, 21		HP:0200134	PMID:24399846	PCS		4/4			P	HPO:skoehler[2014-07-11];HPO:probinson[2022-10-18]
OMIM:182900	Spherocytosis, type 1		HP:0005502	PMID:17327413	PCS		7/12			P	HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0003621	PMID:17327413	PCS		2/13			C	HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0004444	PMID:17327413	PCS		13/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0003593	PMID:17327413	PCS		1/13			C	HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0001081	OMIM:182900	IEA					P	HPO:iea[2009-02-17]
OMIM:182900	Spherocytosis, type 1		HP:0011463	PMID:17327413	PCS		1/13			C	HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0002904	OMIM:182900	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0001878	PMID:17327413	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0000007	PMID:17327413	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0001923	PMID:17327413	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0000006	PMID:17327413	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0000952	PMID:17327413	PCS		12/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0001744	PMID:17327413	PCS		6/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-03]
OMIM:182900	Spherocytosis, type 1		HP:0003623	PMID:17327413	PCS		9/13			C	HPO:probinson[2022-04-03]
OMIM:601846	Vacuolar neuromyopathy		HP:0002015	OMIM:601846	TAS					P	HPO:probinson[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003236	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003555	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003687	OMIM:601846	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0001761	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003581	OMIM:601846	IEA					C	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003691	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0002460	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003560	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0001618	OMIM:601846	TAS					P	HPO:probinson[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003828	OMIM:601846	IEA					M	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0009027	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003805	OMIM:601846	TAS					P	HPO:probinson[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003547	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0000006	OMIM:601846	IEA					I	HPO:iea[2009-02-17]
OMIM:601846	Vacuolar neuromyopathy		HP:0003722	OMIM:601846	IEA					P	HPO:iea[2009-02-17]
OMIM:614293	Hydatidiform mole, recurrent, 2		HP:0032192	PMID:23232697	PCS		3/3			P	HPO:probinson[2019-04-20]
OMIM:614293	Hydatidiform mole, recurrent, 2		HP:0000007	PMID:23232697	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2019-04-20]
OMIM:616490	Joubert syndrome 23		HP:0006989	PMID:26096313	PCS		1/9			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0000496	PMID:26096313	PCS		6/6			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0000407	PMID:26096313	PCS		1/9			P	HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0007033	PMID:26096313	PCS		1/9			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0001263	PMID:26096313	PCS		5/5			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0000007	PMID:26096313	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0010442	PMID:26096313	PCS	HP:0003577	1/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0002789	PMID:26096313	PCS		5/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0000589	PMID:26096313	PCS	HP:0003577	1/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:616490	Joubert syndrome 23		HP:0002104	PMID:26096313	PCS		4/8			P	HPO:skoehler[2015-08-05];HPO:probinson[2023-01-18]
OMIM:242550	Ichthyosis, split hairs, and amino aciduria		HP:0001595	OMIM:242550	IEA					P	HPO:iea[2009-02-17]
OMIM:242550	Ichthyosis, split hairs, and amino aciduria		HP:0003355	OMIM:242550	IEA					P	HPO:iea[2009-02-17]
OMIM:242550	Ichthyosis, split hairs, and amino aciduria		HP:0007431	OMIM:242550	TAS					P	HPO:skoehler[2009-02-17]
OMIM:242550	Ichthyosis, split hairs, and amino aciduria		HP:0000007	OMIM:242550	IEA					I	HPO:iea[2009-02-17]
OMIM:242550	Ichthyosis, split hairs, and amino aciduria		HP:0001249	OMIM:242550	IEA					P	HPO:iea[2009-02-17]
OMIM:235900	Histiocytosis, familial lipochrome		HP:0002113	OMIM:235900	TAS					P	HPO:probinson[2009-02-17]
OMIM:235900	Histiocytosis, familial lipochrome		HP:0005413	OMIM:235900	TAS					P	HPO:probinson[2009-02-17]
OMIM:235900	Histiocytosis, familial lipochrome		HP:0005764	OMIM:235900	TAS					P	HPO:probinson[2009-02-17]
OMIM:235900	Histiocytosis, familial lipochrome		HP:0002719	OMIM:235900	TAS					P	HPO:probinson[2009-02-17]
OMIM:235900	Histiocytosis, familial lipochrome		HP:0000007	OMIM:235900	TAS					I	HPO:probinson[2009-02-17]
OMIM:235900	Histiocytosis, familial lipochrome		HP:0100727	OMIM:235900	IEA					P	HPO:skoehler[2015-01-27]
OMIM:235900	Histiocytosis, familial lipochrome		HP:0010702	OMIM:235900	TAS					P	HPO:probinson[2012-07-18]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002069	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001034	PMID:1372469	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001276	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002861	OMIM:278800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002542	PMID:1372469	PCS		2/2			P	HPO:iea[2011-12-28];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0003510	PMID:1372469	PCS		1/2			P	HPO:probinson[2012-03-18];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0003079	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001036	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000486	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002283	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001251	PMID:1372469	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0010665	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0012407	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0008110	PMID:1372469	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0011463	PMID:1372469	PCS		2/2			C	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0040078	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001009	PMID:1372469	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000656	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002119	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002415	PMID:1372469	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001268	PMID:1372469	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001249	PMID:1372469	PCS		2/2			P	HPO:probinson[2012-03-18];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001029	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0008639	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001265	PMID:1372469	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002135	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0002059	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000252	PMID:1372469	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000992	PMID:1372469	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0004334	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0003487	PMID:1372469	PCS		2/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001266	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000491	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0025455	PMID:1372469	PCS		2/2			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001263	PMID:1372469	PCS		2/2			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001284	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000407	PMID:1372469	PCS		1/2			P	HPO:probinson[2012-03-18];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000509	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0009830	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000007	PMID:10767341	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000648	PMID:1372469	PCS		1/2			P	HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0008689	PMID:1372469	PCS		1/1			P	HPO:probinson[2022-04-10];HPO:probinson[2022-04-10]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0001257	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:278800	De Sanctis-Cacchione syndrome		HP:0000621	OMIM:278800	IEA					P	HPO:iea[2009-02-17]
OMIM:609981	Immunodeficiency 54		HP:0005523	OMIM:609981	TAS					P	HPO:skoehler[2013-05-31]
OMIM:609981	Immunodeficiency 54		HP:0000252	PMID:22354167	PCS		3/4			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0004322	PMID:22354167	PCS		5/6			P	HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0011749	PMID:22354170	PCS					P	HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0002240	OMIM:609981	TAS					P	HPO:skoehler[2012-12-02]
OMIM:609981	Immunodeficiency 54		HP:0002093	OMIM:609981	TAS		HP:0040283			P	HPO:skoehler[2012-12-02]
OMIM:609981	Immunodeficiency 54		HP:0011410	PMID:22354167	PCS		5/6			P	HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0001508	PMID:22354170	PCS		5/8			P	HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0011342	PMID:22354167	PCS		5/6			P	HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0040012	PMID:22354170	PCS					P	HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0000007	PMID:22354167	PCS					I	HPO:skoehler[2012-12-02];HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0002716	OMIM:609981	TAS					P	HPO:skoehler[2012-12-02]
OMIM:609981	Immunodeficiency 54		HP:0000953	PMID:22354170	PCS		5/8			P	HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0000846	PMID:22354167	PCS		6/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0008897	PMID:22354167	PCS					P	HPO:skoehler[2012-12-02];HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0002878	OMIM:609981	TAS		HP:0040283			P	HPO:skoehler[2014-06-24]
OMIM:609981	Immunodeficiency 54		HP:0004429	PMID:22354167	PCS		6/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0001511	PMID:22354167	PCS		6/6			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0002205	PMID:22354170	PCS		1/7			P	HPO:skoehler[2012-12-02];HPO:probinson[2021-05-30]
OMIM:609981	Immunodeficiency 54		HP:0001744	OMIM:609981	TAS					P	HPO:skoehler[2012-12-02]
OMIM:609981	Immunodeficiency 54		HP:0040218	PMID:22354167	PCS		6/6			P	HPO:probinson[2021-05-30]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0007715	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0002650	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0031936	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0001640	PMID:30701273	PCS	HP:0003593	1/2			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0002792	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0002460	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0001290	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0100295	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0002093	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0030319	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0031237	PMID:30701273	PCS		2/2			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0008872	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0001635	PMID:30701273	PCS	HP:0003593	1/2			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0020202	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0000218	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0003803	PMID:30701273	PCS		2/2			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0001324	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0003701	PMID:30701273	PCS	HP:0011463				P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0000597	PMID:30701273	PCS					P	HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0000006	PMID:30701273	PCS					I	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618654	Myopathy, congenital with structured cores and Z-line abnormalities		HP:0003557	PMID:30701273	PCS		2/2			P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:610208	Migraine with or without aura, susceptibility to, 10		HP:0002013	OMIM:610208	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610208	Migraine with or without aura, susceptibility to, 10		HP:0002077	OMIM:610208	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610208	Migraine with or without aura, susceptibility to, 10		HP:0000613	OMIM:610208	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610208	Migraine with or without aura, susceptibility to, 10		HP:0002083	OMIM:610208	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610208	Migraine with or without aura, susceptibility to, 10		HP:0002183	OMIM:610208	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610208	Migraine with or without aura, susceptibility to, 10		HP:0002018	OMIM:610208	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610208	Migraine with or without aura, susceptibility to, 10		HP:0000006	OMIM:610208	IEA					I	HPO:skoehler[2010-06-19]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002188	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001250	PMID:27694961	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000160	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0003196	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001252	PMID:27694961	PCS		2/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0003593	PMID:27694961	PCS		2/7			C	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001251	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0012469	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0009540	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000316	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002539	PMID:27694961	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000678	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000311	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0020049	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001249	PMID:27694961	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0003623	PMID:27694961	PCS		2/7			C	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000175	PMID:27694961	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001344	PMID:27694961	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002079	PMID:27694961	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0011968	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000490	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001263	PMID:27694961	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0004691	PMID:27694961	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002194	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002190	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0010712	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0006380	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000407	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0004209	PMID:27694961	PCS		2/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000520	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000201	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000006	PMID:27694961	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0034391	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002521	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0003577	PMID:27694961	PCS		5/7			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0010705	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000463	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002121	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002282	PMID:27694961	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001629	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001508	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0100704	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0008936	PMID:27694961	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0001762	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000750	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000276	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0032388	PMID:27694961	PCS		7/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0032988	PMID:27694961	PCS		2/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0009471	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000308	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000543	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000268	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0002126	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000545	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000347	PMID:27694961	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000666	PMID:27694961	PCS		1/7			P	HPO:probinson[2023-02-10]
OMIM:617201	Periventricular nodular heterotopia 7		HP:0000028	PMID:27694961	PCS		1/3	MALE		P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-10]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0003577	PMID:20637498	PCS		6/7			C	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001252	PMID:20637498	PCS		7/7			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0003593	PMID:20637498	PCS		1/7			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001270	PMID:20637498	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000639	PMID:20637498	PCS		7/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000518	PMID:20637498	PCS		2/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000958	PMID:20637498	PCS		5/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001508	PMID:20637498	PCS		2/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000316	OMIM:612379	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000998	OMIM:612379	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0002910	PMID:20637498	PCS		6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001249	PMID:20637498	PCS		7/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000973	OMIM:612379	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001320	PMID:20637498	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0003642	PMID:20637498	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000572	PMID:20637498	PCS		7/7			P	HPO:skoehler[2013-06-03];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001000	OMIM:612379	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0002015	PMID:20637498	PCS		2/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001263	PMID:20637498	PCS		4/4			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0003186	PMID:20637498	PCS		2/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0005280	OMIM:612379	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0008064	PMID:20637498	PCS		4/7			P	HPO:skoehler[2015-07-29];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000007	PMID:20637498	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000964	PMID:20637498	PCS		5/7			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001976	PMID:20637498	PCS		5/5			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000568	PMID:20637498	PCS		2/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001935	PMID:20637498	PCS		5/7			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000648	PMID:20637498	PCS		5/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0001257	PMID:20637498	PCS		2/7			P	HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000248	OMIM:612379	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000589	PMID:20637498	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2022-07-16]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000369	OMIM:612379	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0002126	OMIM:612379	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612379	Congenital disorder of glycosylation, type IQ		HP:0000962	OMIM:612379	IEA					P	HPO:skoehler[2010-06-20]
OMIM:615402	Dyschromatosis universalis hereditaria 3		HP:0001034	PMID:23519333	PCS	HP:0011463				P	HP:probinson[2019-03-02]
OMIM:615402	Dyschromatosis universalis hereditaria 3		HP:0020073	PMID:23519333	PCS	HP:0011463				P	HP:probinson[2019-03-02]
OMIM:615402	Dyschromatosis universalis hereditaria 3		HP:0011463	PMID:23519333	PCS					C	HPO:probinson[2022-08-15]
OMIM:615402	Dyschromatosis universalis hereditaria 3		HP:0000006	PMID:23519333	PCS					I	HPO:skoehler[2013-09-30];HP:probinson[2019-03-02]
OMIM:312830	Scarf syndrome		HP:0000286	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0003312	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000343	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000486	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000023	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0001552	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0004443	OMIM:312830	IEA					P	HPO:iea[2012-02-24]
OMIM:312830	Scarf syndrome		HP:0002162	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0004440	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0008070	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0006297	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000879	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0002557	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0006610	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000358	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0001249	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000973	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0001540	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000054	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000494	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000431	OMIM:312830	TAS					P	HPO:probinson[2012-05-01]
OMIM:312830	Scarf syndrome		HP:0000331	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000474	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000051	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000294	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000470	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0001419	OMIM:312830	IEA					I	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000508	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0001537	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000426	OMIM:312830	TAS					P	HPO:probinson[2012-05-01]
OMIM:312830	Scarf syndrome		HP:0000768	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000048	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000465	OMIM:312830	TAS					P	HPO:probinson[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000028	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:312830	Scarf syndrome		HP:0000369	OMIM:312830	IEA					P	HPO:iea[2009-02-17]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0100864	PMID:19615667	PCS	HP:0003593	2/2			P	HPO:probinson[2013-04-14];HPO:probinson[2022-06-05]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0002983	PMID:19615667	PCS		0/2			P	HPO:probinson[2013-04-14];HPO:probinson[2022-06-05]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0003016	PMID:19615667	PCS	HP:0003593	2/2			P	HPO:probinson[2015-03-08];HPO:probinson[2022-06-05]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0003025	PMID:19615667	PCS	HP:0003593	2/2			P	HPO:probinson[2013-04-14];HPO:probinson[2022-06-05]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0002970	PMID:19615667	PCS		2/2			P	HPO:probinson[2022-06-05]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0003593	PMID:19615667	PCS		2/2			C	HPO:probinson[2022-06-05]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0002979	PMID:19615667	PCS		2/2			P	HPO:probinson[2013-04-14];HPO:probinson[2022-06-05]
OMIM:613073	Metaphyseal anadysplasia 2		HP:0000007	PMID:19615667	PCS					I	HPO:probinson[2013-04-14]
OMIM:618126	Liddle syndrome 3		HP:0003351	PMID:28710092	PCS		2/2			P	HPO:probinson[2023-04-08]
OMIM:618126	Liddle syndrome 3		HP:0000822	PMID:28710092	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-04-08]
OMIM:618126	Liddle syndrome 3		HP:0200114	PMID:28710092	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-04-08]
OMIM:618126	Liddle syndrome 3		HP:0002900	PMID:28710092	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-04-08]
OMIM:618126	Liddle syndrome 3		HP:0004319	PMID:28710092	PCS		2/2			P	HPO:probinson[2023-04-08]
OMIM:618126	Liddle syndrome 3		HP:0000006	PMID:28710092	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-04-08]
OMIM:601477	Ribbing disease		HP:0003034	OMIM:601477	TAS					P	HPO:skoehler[2009-02-17]
OMIM:601477	Ribbing disease		HP:0000007	OMIM:601477	IEA					I	HPO:iea[2009-02-17]
OMIM:619238	Immunodeficiency 79		HP:0003621	PMID:31781092	PCS		1/1			C	HPO:probinson[2021-05-08]
OMIM:619238	Immunodeficiency 79		HP:0000007	PMID:31781092	PCS					I	HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:619238	Immunodeficiency 79		HP:0033004	PMID:31781092	PCS		1/1		HP:0031375	P	HPO:probinson[2021-05-08]
OMIM:619238	Immunodeficiency 79		HP:0000403	PMID:33471124	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:619238	Immunodeficiency 79		HP:0033005	PMID:31781092	PCS		1/1		HP:0031375	P	HPO:probinson[2021-05-08]
OMIM:619238	Immunodeficiency 79		HP:0002788	PMID:33471124	PCS		1/1			P	HPO:probinson[2021-05-08]
OMIM:619238	Immunodeficiency 79		HP:0032215	PMID:33471124	IEA		1/1			P	HPO:probinson[2021-05-08];HPO:probinson[2021-05-08]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0003577	PMID:17098888	PCS		10/10			C	HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0008619	PMID:17098888	PCS	HP:0003577	10/10			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0001751	PMID:17098888	PCS		0/10			P	HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0003251	PMID:17098888	PCS	HP:0011462	3/3			P	HPO:skoehler[2015-01-21];HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0000007	PMID:17098888	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0012207	PMID:17098888	PCS		3/3			P	HPO:probinson[2013-03-12];HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0012868	PMID:17098888	PCS		3/3			P	HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0008669	PMID:17098888	PCS		3/3			P	HPO:probinson[2012-07-22];HPO:probinson[2022-06-22]
OMIM:611102	Deafness, sensorineural, and male infertility		HP:0012865	PMID:17098888	PCS		3/3			P	HPO:probinson[2022-06-22]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0001000	OMIM:225050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0012265	OMIM:225050	TAS					P	HPO:probinson[2013-04-07]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0001025	OMIM:225050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0007607	OMIM:225050	IEA					P	HPO:iea[2009-02-17]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0002164	OMIM:225050	IEA					P	HPO:iea[2009-02-17]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0002719	OMIM:225050	IEA					P	HPO:iea[2009-02-17]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0002209	OMIM:225050	IEA					P	HPO:iea[2009-02-17]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0000007	OMIM:225050	IEA					I	HPO:iea[2009-02-17]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0000832	OMIM:225050	IEA					P	HPO:iea[2009-02-17]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0005938	OMIM:225050	TAS					P	HPO:probinson[2013-04-07]
OMIM:225050	Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliarydyskinesia		HP:0045075	OMIM:225050	TAS					P	HPO:probinson[2022-05-07]
OMIM:268150	Anemia, hemolytic, Rh-null, Regulator type		HP:0004446	OMIM:268150	IEA					P	HPO:iea[2009-02-17]
OMIM:268150	Anemia, hemolytic, Rh-null, Regulator type		HP:0005502	OMIM:268150	IEA					P	HPO:iea[2009-02-17]
OMIM:268150	Anemia, hemolytic, Rh-null, Regulator type		HP:0008282	OMIM:268150	IEA					P	HPO:iea[2009-02-17]
OMIM:268150	Anemia, hemolytic, Rh-null, Regulator type		HP:0001878	OMIM:268150	IEA					P	HPO:iea[2009-02-17]
OMIM:268150	Anemia, hemolytic, Rh-null, Regulator type		HP:0000952	OMIM:268150	IEA					P	HPO:iea[2009-02-17]
OMIM:268150	Anemia, hemolytic, Rh-null, Regulator type		HP:0000006	OMIM:268150	TAS					I	HPO:skoehler[2019-04-18]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000483	PMID:34089229	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000486	PMID:30950035	PCS		1/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0002540	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0004322	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001252	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001251	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0003593	PMID:30950035	PCS		3/3			C	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001290	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0032794	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0012471	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0003429	PMID:34089229	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001324	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0002415	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000278	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001249	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000252	PMID:34089229	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000692	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001344	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0004411	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0002310	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0011968	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001260	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001263	PMID:34089229;PMID:30950035	PCS		5/5			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001182	PMID:34089229	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0005180	PMID:30950035	PCS	HP:0003621	3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0012385	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000448	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000007	PMID:30950035	PCS					I	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000648	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000565	PMID:34089229	PCS		2/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001257	PMID:34089229;PMID:30950035	PCS		4/5			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001653	PMID:30950035	PCS	HP:0003621	3/3			P	HPO:probinson[2021-11-27];HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000340	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001310	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001272	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0002120	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0011712	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0030084	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001302	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001347	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000154	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0002015	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0002650	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000426	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0001510	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000545	PMID:34089229;PMID:30950035	PCS		3/5			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000666	PMID:30950035	PCS		3/3			P	HPO:probinson[2021-11-27]
OMIM:619576	Cerebellar ataxia, brain abnormalities, and cardiac conduction defects		HP:0000303	PMID:34089229	PCS		1/2			P	HPO:probinson[2021-11-27]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0002059	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0006813	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0002188	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0002540	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0002133	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0002376	OMIM:616645	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0003781	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0001250	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0001263	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0003593	PMID:26333769	PCS					C	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0005484	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0007256	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0000007	OMIM:616645	TAS					I	HPO:skoehler[2017-07-13]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0007334	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0007359	PMID:26333769	PCS					P	HPO:probinson[2017-06-17]
OMIM:616645	Epileptic encephalopathy, early infantile, 34		HP:0001249	OMIM:616645	TAS					P	HPO:skoehler[2017-07-13]
OMIM:272120	Sudden infant death syndrome		HP:0002047	OMIM:272120	TAS					P	HPO:skoehler[2018-10-08]
OMIM:272120	Sudden infant death syndrome		HP:0005949	OMIM:272120	TAS					P	HPO:skoehler[2010-06-20]
OMIM:272120	Sudden infant death syndrome		HP:0000007	OMIM:272120	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:272120	Sudden infant death syndrome		HP:0001426	OMIM:272120	TAS					I	HPO:nvasilevsky[2019-03-12]
OMIM:272120	Sudden infant death syndrome		HP:0001699	OMIM:272120	TAS					P	HPO:skoehler[2012-07-18]
OMIM:607748	Hypercholanemia, familial		HP:0002630	OMIM:607748	TAS					P	HPO:probinson[2013-03-04]
OMIM:607748	Hypercholanemia, familial		HP:0011892	OMIM:607748	TAS					P	HPO:probinson[2013-03-04]
OMIM:607748	Hypercholanemia, familial		HP:0001508	OMIM:607748	TAS					P	HPO:probinson[2013-03-04]
OMIM:607748	Hypercholanemia, familial		HP:0002570	OMIM:607748	TAS					P	HPO:probinson[2013-03-04]
OMIM:607748	Hypercholanemia, familial		HP:0002748	OMIM:607748	TAS					P	HPO:probinson[2013-03-04]
OMIM:607748	Hypercholanemia, familial		HP:0000007	OMIM:607748	TAS					I	HPO:probinson[2013-01-09]
OMIM:607748	Hypercholanemia, familial		HP:0000989	OMIM:607748	TAS					P	HPO:probinson[2013-03-04]
OMIM:607748	Hypercholanemia, familial		HP:0012202	OMIM:607748	TAS					P	HPO:probinson[2013-03-12]
OMIM:220100	Cystinuria		HP:0003532	OMIM:220100	TAS					P	HPO:probinson[2012-07-26]
OMIM:220100	Cystinuria		HP:0003268	OMIM:220100	TAS					P	HPO:probinson[2012-07-26]
OMIM:220100	Cystinuria		HP:0000010	OMIM:220100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220100	Cystinuria		HP:0003297	OMIM:220100	TAS					P	HPO:probinson[2012-07-26]
OMIM:220100	Cystinuria		HP:0000083	OMIM:220100	TAS					P	HPO:skoehler[2012-10-17]
OMIM:220100	Cystinuria		HP:0003131	OMIM:220100	TAS					P	HPO:probinson[2009-02-17]
OMIM:220100	Cystinuria		HP:0000007	OMIM:220100	TAS					I	HPO:skoehler[2012-10-17]
OMIM:220100	Cystinuria		HP:0000787	OMIM:220100	IEA					P	HPO:iea[2009-02-17]
OMIM:220100	Cystinuria		HP:0000006	OMIM:220100	TAS					I	HPO:skoehler[2012-10-17]
OMIM:153630	MACROGLOSSIA		HP:0000158	OMIM:153630	IEA					P	HPO:iea[2009-02-17]
OMIM:153630	MACROGLOSSIA		HP:0000006	OMIM:153630	IEA					I	HPO:iea[2009-02-17]
OMIM:115665	Cataract, congenital, Volkmann type		HP:0100018	PMID:7607651	PCS	HP:0003577	41/41			P	HPO:iea[2012-07-31]
OMIM:115665	Cataract, congenital, Volkmann type		HP:0000529	PMID:7607651	PCS					P	HPO:iea[2009-02-17]
OMIM:115665	Cataract, congenital, Volkmann type		HP:0000519	OMIM:115665	TAS					P	HPO:skoehler[2012-10-17]
OMIM:115665	Cataract, congenital, Volkmann type		HP:0000006	OMIM:115665	PCS					I	HPO:iea[2009-02-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001298	OMIM:614052	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0003577	PMID:18953340;OMIM:614052	PCS		35/35			C	HPO:probinson[2022-08-27];HPO:skoehler[2012-11-20]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000343	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000463	OMIM:614052	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000023	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001250	OMIM:614052	TAS		HP:0040283			P	HPO:skoehler[2014-08-24]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001271	PMID:18953340	PCS		1/25			P	HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001252	PMID:18953340	PCS		19/25			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001251	OMIM:614052	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001290	OMIM:614052	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0011675	OMIM:614052	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0012368	OMIM:614052	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0002080	OMIM:614052	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000518	OMIM:614052	TAS		HP:0040283			P	HPO:skoehler[2012-11-20]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001508	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001987	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0002578	OMIM:614052	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0003348	OMIM:614052	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0003128	PMID:18953340	PCS		25/25			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001622	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0005469	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001562	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000431	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0002352	OMIM:614052	TAS					P	HPO:skoehler[2014-08-24]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0011925	PMID:18953340	PCS		25/25			P	HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001263	PMID:18953340;OMIM:614052	PCS		30/30			P	HPO:skoehler[2019-02-22];HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0002151	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0002093	OMIM:614052	TAS	HP:0003623				P	HPO:skoehler[2012-11-20]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0003819	PMID:18953340	PCS		4/25			C	HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001639	PMID:18953340	PCS		22/25			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000308	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001518	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000822	OMIM:614052	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001537	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000007	PMID:18953340	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001511	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0003811	PMID:18953340	PCS		8/25			C	HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000047	PMID:18953340	PCS		7/13	MALE		P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001510	PMID:18953340	PCS		10/25			P	HPO:probinson[2022-08-27];HPO:probinson[2022-08-27]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000028	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0000369	OMIM:614052	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0001337	OMIM:614052	TAS					P	HPO:skoehler[2012-11-20]
OMIM:614052	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2		HP:0003535	PMID:18953340	PCS		20/25			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-27]
OMIM:612423	Prekallikrein deficiency		HP:0001892	PMID:15461630	PCS		0/1			P	HPO:probinson[2013-04-14];HPO:probinson[2022-08-28]
OMIM:612423	Prekallikrein deficiency		HP:0034371	PMID:15461630	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:612423	Prekallikrein deficiency		HP:0003584	PMID:15461630	PCS		1/1			C	HPO:probinson[2022-08-28]
OMIM:612423	Prekallikrein deficiency		HP:0000007	PMID:15461630	PCS					I	HPO:probinson[2013-04-14]
OMIM:612423	Prekallikrein deficiency		HP:0003645	PMID:15461630	PCS		1/1			P	HPO:probinson[2013-04-14];HPO:probinson[2022-08-28]
OMIM:269500	Sclerosteosis 1		HP:0001474	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0001133	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0010628	OMIM:269500	IEA					P	HPO:skoehler[2018-10-08]
OMIM:269500	Sclerosteosis 1		HP:0000365	OMIM:269500	TAS					P	HPO:probinson[2012-05-01]
OMIM:269500	Sclerosteosis 1		HP:0001233	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0002164	PMID:35208525	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0100543	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0000639	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0000858	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0007285	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0000916	OMIM:269500	TAS					P	HPO:probinson[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0001548	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0100729	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000316	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0002516	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0002315	PMID:35208525	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000336	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0006415	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0000572	PMID:35208525	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000692	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000431	OMIM:269500	IEA					P	HPO:iea[2012-05-01]
OMIM:269500	Sclerosteosis 1		HP:0004576	PMID:35208525	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0001085	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0002690	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000272	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0004097	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0011800	OMIM:269500	TAS					P	HPO:skoehler[2013-11-28]
OMIM:269500	Sclerosteosis 1		HP:0005280	OMIM:269500	IEA					P	HPO:iea[2012-05-01]
OMIM:269500	Sclerosteosis 1		HP:0025709	PMID:35208525	PCS		1/1			C	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0002829	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000689	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0000007	PMID:11179006	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000648	PMID:35208525	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0001159	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0002007	PMID:35208525	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000565	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0000520	PMID:35208525	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000303	PMID:35208525	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0000622	PMID:35208525	PCS		1/1			P	HPO:probinson[2022-09-28]
OMIM:269500	Sclerosteosis 1		HP:0001699	OMIM:269500	TAS					P	HPO:probinson[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0000885	OMIM:269500	TAS					P	HPO:probinson[2009-02-17]
OMIM:269500	Sclerosteosis 1		HP:0002644	OMIM:269500	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0003510	OMIM:224400	IEA					P	HPO:skoehler[2015-01-21]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0002983	OMIM:224400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0003016	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0001376	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0003375	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0002084	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0012368	OMIM:224400	TAS					P	HPO:skoehler[2013-10-22]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0008110	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000238	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000774	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000311	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000773	OMIM:224400	TAS					P	HPO:probinson[2010-06-18]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0001007	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0003026	OMIM:224400	TAS					P	HPO:probinson[2012-05-08]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000175	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0005622	OMIM:224400	TAS					P	HPO:probinson[2012-05-08]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0004233	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000272	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000470	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0012019	OMIM:224400	IEA					P	HPO:skoehler[2018-10-08]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0011800	OMIM:224400	TAS					P	HPO:skoehler[2013-11-28]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0001083	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0001181	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0012385	OMIM:224400	TAS					P	HPO:skoehler[2013-10-22]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0009473	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000007	OMIM:224400	IEA					I	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0006487	OMIM:224400	TAS					P	HPO:probinson[2012-05-08]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0008921	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000586	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000347	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:224400	Dyssegmental dysplasia, Rolland-Desbuquois type		HP:0000501	OMIM:224400	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-Ichthyosis-Deafness syndrome, autosomal dominant		HP:0002221	PMID:11918723	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0002860	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000221	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0002164	OMIM:148210	TAS					P	HPO:skoehler[2012-11-21]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0012804	OMIM:148210	TAS					P	HPO:skoehler[2015-01-20]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0001097	PMID:11918723	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-Ichthyosis-Deafness syndrome, autosomal dominant		HP:0045075	PMID:11918723	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000618	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000613	PMID:11918723	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000559	OMIM:148210	TAS					P	HPO:skoehler[2012-11-26]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000653	PMID:11918723	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0005406	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0001128	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-Ichthyosis-Deafness syndrome, autosomal dominant		HP:0002555	PMID:11918723	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-Ichthyosis-Deafness syndrome, autosomal dominant		HP:0003623	PMID:11918723	PCS		1/1			C	HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000495	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0001761	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-Ichthyosis-Deafness syndrome, autosomal dominant		HP:0000491	PMID:11918723	PCS	HP:0011463	1/1			P	HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-Ichthyosis-Deafness syndrome, autosomal dominant		HP:0000691	PMID:11918723	PCS		1/1			P	HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0006380	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0008064	PMID:11918723	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000407	PMID:11918723	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000966	PMID:11918723	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0008404	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0002745	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0002987	OMIM:148210	IEA					P	HPO:iea[2009-02-17]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000006	PMID:11918723	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:148210	Keratitis-ichthyosis-deafness syndrome		HP:0000962	PMID:11918723	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-07]
OMIM:193400	von Willebrand disease, type 1		HP:0003125	OMIM:193400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:193400	von Willebrand disease, type 1		HP:0000132	OMIM:193400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:193400	von Willebrand disease, type 1		HP:0001650	OMIM:193400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:193400	von Willebrand disease, type 1		HP:0005542	OMIM:193400	IEA					P	HPO:iea[2009-02-17]
OMIM:193400	von Willebrand disease, type 1		HP:0003540	OMIM:193400	IEA					P	HPO:iea[2009-02-17]
OMIM:193400	von Willebrand disease, type 1		HP:0000471	OMIM:193400	IEA					P	HPO:iea[2009-02-17]
OMIM:193400	von Willebrand disease, type 1		HP:0003010	OMIM:193400	IEA					P	HPO:iea[2009-02-17]
OMIM:193400	von Willebrand disease, type 1		HP:0005261	OMIM:193400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:193400	von Willebrand disease, type 1		HP:0012147	OMIM:193400	TAS					P	HPO:probinson[2021-02-26]
OMIM:193400	von Willebrand disease, type 1		HP:0003829	OMIM:193400	TAS					I	HPO:skoehler[2012-10-17]
OMIM:193400	von Willebrand disease, type 1		HP:0006298	PMID:12649144	PCS		4/12			P	HPO:probinson[2021-02-26]
OMIM:193400	von Willebrand disease, type 1		HP:0000978	PMID:12649144	PCS		5/12			P	HPO:skoehler[2010-06-20];HPO:probinson[2021-02-26]
OMIM:193400	von Willebrand disease, type 1		HP:0001934	PMID:12649144	PCS		4/12			P	HPO:probinson[2021-02-26]
OMIM:193400	von Willebrand disease, type 1		HP:0004846	PMID:12649144	PCS		4/12			P	HPO:probinson[2021-02-26]
OMIM:193400	von Willebrand disease, type 1		HP:0002239	OMIM:193400	IEA					P	HPO:iea[2009-02-17]
OMIM:193400	von Willebrand disease, type 1		HP:0000421	PMID:12649144	PCS		8/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2021-02-26]
OMIM:193400	von Willebrand disease, type 1		HP:0001634	OMIM:193400	IEA					P	HPO:iea[2009-02-17]
OMIM:193400	von Willebrand disease, type 1		HP:0000006	OMIM:193400	IEA					I	HPO:iea[2009-02-17]
OMIM:611880	Cardiomyopathy, dilated, 2A		HP:0031318	PMID:15070570	PCS		0/1			P	HPO:probinson[2022-07-04]
OMIM:611880	Cardiomyopathy, dilated, 2A		HP:0031319	PMID:15070570	PCS		1/1			P	HPO:probinson[2022-07-04]
OMIM:611880	Cardiomyopathy, dilated, 2A		HP:0011462	PMID:15070570	PCS		2/2			C	HPO:probinson[2014-05-24];HPO:probinson[2022-07-04]
OMIM:611880	Cardiomyopathy, dilated, 2A		HP:0001635	PMID:15070570	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:611880	Cardiomyopathy, dilated, 2A		HP:0000007	PMID:15070570	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:611880	Cardiomyopathy, dilated, 2A		HP:0033755	PMID:15070570	PCS		1/2			P	HPO:probinson[2022-07-04]
OMIM:611880	Cardiomyopathy, dilated, 2A		HP:0001644	PMID:15070570	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-07-04]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0002322	PMID:11462174	PCS		1/4			P	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0002067	PMID:11462174	PCS		4/4			P	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0031959	PMID:12953260	PCS		1/2			P	HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0003581	PMID:11462174	PCS					C	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0002063	PMID:11462174	PCS		4/4			P	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0002174	PMID:11462174	PCS		3/4			P	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0100660	PMID:12953260	TAS		1/2			P	HP:probinson[2019-05-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0000739	PMID:12953260	PCS		2/2			P	HPO:skoehler[2010-06-20];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0000007	PMID:11462174	PCS					I	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0000725	PMID:11462174	PCS		1/4			P	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0002548	PMID:11462174;PMID:12953260	PCS		4/4			P	HP:probinson[2019-05-17];HP:probinson[2019-05-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0003677	PMID:11462174	PCS		4/4			C	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0001348	PMID:11462174	PCS		3/4			P	HP:probinson[2019-05-17]
OMIM:606324	Parkinson disease 7, autosomal recessive early-onset		HP:0000643	PMID:11462174	PCS		1/4			P	HPO:iea[2009-02-17];HP:probinson[2019-05-17]
OMIM:260530	Parana hard-skin syndrome		HP:0001438	OMIM:260530	IEA					P	HPO:iea[2009-02-17]
OMIM:260530	Parana hard-skin syndrome		HP:0000007	OMIM:260530	IEA					I	HPO:iea[2009-02-17]
OMIM:260530	Parana hard-skin syndrome		HP:0006596	OMIM:260530	IEA					P	HPO:iea[2009-02-17]
OMIM:260530	Parana hard-skin syndrome		HP:0008850	OMIM:260530	IEA					P	HPO:iea[2009-02-17]
OMIM:260530	Parana hard-skin syndrome		HP:0002093	OMIM:260530	IEA					P	HPO:iea[2009-02-17]
OMIM:260530	Parana hard-skin syndrome		HP:0000951	OMIM:260530	IEA					P	HPO:iea[2009-02-17]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0003676	PMID:18976727	PCS					C	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-18]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0003621	PMID:18976727	PCS					C	HPO:probinson[2023-02-18]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0001310	OMIM:612437	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0002123	PMID:18976727	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-18]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0003487	OMIM:612437	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0001260	OMIM:612437	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0010819	OMIM:612437	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0001251	PMID:18976727	PCS					P	HPO:probinson[2023-02-18]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0000007	PMID:18976727	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-18]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0003390	OMIM:612437	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0001337	OMIM:612437	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612437	Epilepsy, progressive myoclonic 1B		HP:0001336	PMID:18976727	PCS					P	HPO:probinson[2023-02-18]
OMIM:113200	Brachydactyly, type D		HP:0010077	OMIM:113200	TAS					P	HPO:iea[2012-06-10]
OMIM:113200	Brachydactyly, type D		HP:0009642	OMIM:113200	TAS					P	HPO:iea[2009-02-17]
OMIM:113200	Brachydactyly, type D		HP:0005627	OMIM:113200	TAS					P	HPO:iea[2009-02-17]
OMIM:113200	Brachydactyly, type D		HP:0000006	OMIM:113200	TAS					I	HPO:iea[2009-02-17]
OMIM:155255	MEDULLOBLASTOMA		HP:0001442	OMIM:155255	TAS					I	HPO:probinson[2020-07-14]
OMIM:155255	MEDULLOBLASTOMA		HP:0003829	OMIM:155255	TAS					I	HPO:skoehler[2017-07-13]
OMIM:155255	MEDULLOBLASTOMA		HP:0000007	OMIM:155255	TAS					I	HPO:skoehler[2017-07-13]
OMIM:155255	MEDULLOBLASTOMA		HP:0000006	OMIM:155255	TAS					I	HPO:probinson[2009-02-17]
OMIM:155255	MEDULLOBLASTOMA		HP:0002885	OMIM:155255	TAS					P	HPO:probinson[2009-02-17]
OMIM:619562	Joubert syndrome 39		HP:0001320	PMID:33791682	PCS		1/8			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0030674	PMID:33791682	PCS		8/8			C	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0002085	PMID:33791682	PCS		5/8			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0001263	PMID:33791682	PCS		4/4			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0004383	PMID:33791682	PCS	HP:0011461	1/8			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0100259	PMID:33791682	PCS		2/8			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0040213	PMID:33791682	PCS		1/4			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0009183	PMID:33791682	PCS		2/4			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0007021	PMID:33791682	PCS		1/4			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0000657	PMID:33791682	PCS		1/4			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0000007	PMID:33791682	PCS					I	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0002419	PMID:33791682	PCS		2/8			P	HPO:probinson[2021-12-18];HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0025502	PMID:33791682	PCS		2/4			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0000113	PMID:33791682	PCS		1/8			P	HPO:probinson[2021-12-18]
OMIM:619562	Joubert syndrome 39		HP:0000556	PMID:33791682	PCS		4/4			P	HPO:probinson[2021-12-18]
OMIM:616651	Roifman syndrome		HP:0000343	PMID:26522830	PCS		6/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0004322	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000463	PMID:26522830	PCS		6/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0001156	OMIM:616651	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616651	Roifman syndrome		HP:0000460	PMID:26522830	PCS		6/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0001252	PMID:26522830	PCS		5/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0003273	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0002240	PMID:26522830	PCS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0010049	PMID:26522830	PCS		6/6			P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0001290	OMIM:616651	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616651	Roifman syndrome		HP:0001629	PMID:26522830	PCS		1/6			P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0000954	PMID:26522830	PCS		5/6			P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0002716	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000219	PMID:26522830	PCS		6/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0008897	PMID:16901296	PCS		6/6			P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0000637	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0006532	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0002714	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0001744	PMID:26522830	PCS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000556	PMID:26522830	PCS		3/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0001622	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0002655	OMIM:616651	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616651	Roifman syndrome		HP:0003301	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000252	PMID:26522830	PCS		5/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0001880	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000494	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000430	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0012817	PMID:26522830	PCS		1/6			P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0001263	PMID:26522830	PCS		5/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0011927	PMID:26522830	PCS		6/6			P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0006361	PMID:26522830	PCS					P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0011231	OMIM:616651	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616651	Roifman syndrome		HP:0000403	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000964	PMID:26522830	PCS		3/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0000007	PMID:26522830	PCS					I	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0004209	PMID:26522830	PCS		4/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0001511	PMID:16901296	PCS		6/6			P	HPO:skoehler[2015-12-30]
OMIM:616651	Roifman syndrome		HP:0004625	PMID:26522830	PCS					P	HPO:probinson[2017-05-29]
OMIM:616651	Roifman syndrome		HP:0001831	OMIM:616651	TAS					P	HPO:skoehler[2015-12-30]
OMIM:610220	Deafness, autosomal recessive 59		HP:0000407	OMIM:610220	IEA					P	HPO:probinson[2013-03-31]
OMIM:610220	Deafness, autosomal recessive 59		HP:0000007	OMIM:610220	IEA					I	HPO:probinson[2013-01-09]
OMIM:609942	Noonan syndrome 3		HP:0000286	PMID:19396835	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000486	PMID:17056636;PMID:16474405;PMID:19396835	PCS		8/14			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0004322	PMID:17056636;PMID:16474405	PCS		9/12			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0004442	PMID:16474405;PMID:19396835	PCS		2/7			P	HPO:probinson[2021-05-20];HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001250	PMID:17056636	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0003196	PMID:19396835	PCS		1/2			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0004482	PMID:17056636	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000280	PMID:17056636	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0045075	PMID:17056636	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0006191	PMID:17056636	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000639	PMID:17056636;PMID:16474405	PCS		1/12			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000914	PMID:17056636;PMID:16474405	PCS		2/12			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000316	PMID:17056636;PMID:19396835	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001643	OMIM:609942	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609942	Noonan syndrome 3		HP:0000476	PMID:19396835	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001642	PMID:16474405	PCS	HP:0003577	1/5			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001642	PMID:17056636	PCS		3/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0001249	PMID:17056636	PCS		7/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000358	PMID:17056636;PMID:19396835	PCS		4/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000494	PMID:17056636;PMID:19396835	PCS		5/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0002750	OMIM:609942	IEA					P	HPO:skoehler[2019-04-18]
OMIM:609942	Noonan syndrome 3		HP:0011968	PMID:17056636	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0001263	PMID:17056636;PMID:19396835	PCS		9/9			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001582	PMID:17056636	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000767	PMID:17056636;PMID:19396835	PCS		7/9			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:skoehler[2019-04-18];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000768	PMID:17056636;PMID:16474405	PCS		1/12			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000006	PMID:16474405	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000369	PMID:17056636;PMID:19396835	PCS		6/9			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001655	PMID:19396835	PCS		1/2			P	HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0030799	OMIM:609942	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609942	Noonan syndrome 3		HP:0003577	PMID:19396835	PCS		2/2			C	HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000463	PMID:17056636;PMID:19396835	PCS		2/9			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001156	PMID:17056636	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0002162	PMID:17056636	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0012209	PMID:16474405	PCS		1/5			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0008070	PMID:17056636	PCS		2/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0001508	PMID:17056636	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0011321	PMID:19396835	PCS		1/2			P	HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001629	PMID:16474405	PCS		1/5			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001305	PMID:17056636	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000978	PMID:16474405	PCS		1/5			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001869	PMID:17056636	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0001704	PMID:16474405	PCS		1/5			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000218	PMID:19396835	IEA		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-22]
OMIM:609942	Noonan syndrome 3		HP:0006610	PMID:17056636	PCS		0/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0001561	PMID:19396835	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000391	PMID:19396835	PCS		1/2			P	HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000470	PMID:17056636	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0005281	OMIM:609942	IEA					P	HPO:skoehler[2018-10-08]
OMIM:609942	Noonan syndrome 3		HP:0005280	PMID:17056636	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0001639	PMID:17056636;PMID:16474405	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0007099	PMID:19396835	PCS		1/2			P	HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000508	PMID:17056636;PMID:16474405	PCS		7/12			P	HPO:probinson[2021-05-20];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0002967	PMID:17056636	PCS		1/7			P	ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000268	PMID:19396835	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0002007	PMID:19396835	PCS		1/2			P	HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001631	PMID:17056636;PMID:16474405	PCS		2/12			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20];ORCID:0000-0002-0736-9199[2024-06-08]
OMIM:609942	Noonan syndrome 3		HP:0000465	PMID:17056636;PMID:19396835	PCS		5/9			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:probinson[2013-03-31];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0000028	PMID:17056636;PMID:16474405	PCS		3/8			P	ORCID:0000-0002-0736-9199[2024-06-08];HPO:skoehler[2019-04-18];HPO:probinson[2021-05-20]
OMIM:609942	Noonan syndrome 3		HP:0001634	PMID:16474405	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-20]
OMIM:618697	Retinitis pigmentosa 87 with choroidal involvement		HP:0007737	PMID:21654732	PCS					P	HPO:probinson[2020-06-13]
OMIM:618697	Retinitis pigmentosa 87 with choroidal involvement		HP:0000580	PMID:21654732	PCS					P	HPO:probinson[2020-06-13]
OMIM:618697	Retinitis pigmentosa 87 with choroidal involvement		HP:0007994	PMID:21654732	PCS					P	HPO:probinson[2020-06-13]
OMIM:618697	Retinitis pigmentosa 87 with choroidal involvement		HP:0030505	PMID:21654732	PCS					P	HPO:probinson[2020-06-13]
OMIM:618697	Retinitis pigmentosa 87 with choroidal involvement		HP:0000006	PMID:21654732	PCS					I	HPO:probinson[2020-06-13];HPO:probinson[2020-06-13]
OMIM:618697	Retinitis pigmentosa 87 with choroidal involvement		HP:0000533	PMID:21654732	PCS					P	HPO:probinson[2020-06-13]
OMIM:182280	Small cell cancer of the lung		HP:0100526	OMIM:182280	TAS					P	HPO:iea[2009-02-17]
OMIM:182280	Small cell cancer of the lung		HP:0000006	OMIM:182280	TAS					I	HPO:iea[2009-02-17]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0004325	PMID:39471804	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000486	PMID:39471804	PCS		3/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0004322	PMID:39471804	PCS		2/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001332	PMID:39471804	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000122	PMID:39471804	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002020	PMID:39471804	PCS		3/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0003593	PMID:39471804	PCS		3/14			C	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0010442	PMID:39471804	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0011410	PMID:39471804	PCS		4/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0006191	PMID:39471804	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002937	PMID:39471804	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000998	PMID:39471804	PCS		1/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001324	PMID:39471804	PCS		4/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0010290	PMID:39471804	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0003623	PMID:39471804	PCS		2/7			C	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0003763	PMID:39471804	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002553	PMID:39471804	PCS		5/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000494	PMID:39471804	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000252	PMID:39471804	PCS		3/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0031956	PMID:39471804	PCS		6/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001344	PMID:39471804	PCS		1/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0011803	PMID:39471804	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000490	PMID:39471804	PCS		2/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001581	PMID:39471804	PCS		0/8			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0033733	PMID:39471804	PCS		6/8			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0010557	PMID:39471804	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0034392	PMID:39471804	PCS		0/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002827	PMID:39471804	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000007	PMID:39471804	PCS					I	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000527	PMID:39471804	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002028	PMID:39471804	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001276	PMID:39471804	PCS		0/11			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000582	PMID:39471804	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0010946	PMID:39471804	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002002	PMID:39471804	PCS		9/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0003573	PMID:39471804	PCS		1/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002240	PMID:39471804	PCS		5/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0010665	PMID:39471804	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0012202	PMID:39471804	PCS		6/6			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0031964	PMID:39471804	PCS		4/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0100027	PMID:39471804	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000337	PMID:39471804	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002119	PMID:39471804	PCS		2/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000219	PMID:39471804	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0030084	PMID:39471804	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000218	PMID:39471804	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0012171	PMID:39471804	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0006579	PMID:39471804	PCS		1/11			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000750	PMID:39471804	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000232	PMID:39471804	PCS		9/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000194	PMID:39471804	PCS		8/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0011471	PMID:39471804	PCS		0/4			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000902	PMID:39471804	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000508	PMID:39471804	PCS		4/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000989	PMID:39471804	PCS		9/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0100716	PMID:39471804	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002007	PMID:39471804	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0007018	PMID:39471804	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000347	PMID:39471804	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000286	PMID:39471804	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0010804	PMID:39471804	PCS		7/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002188	PMID:39471804	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001250	PMID:39471804	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0003155	PMID:39471804	PCS		12/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:6000950	PMID:39471804	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001252	PMID:39471804	PCS		11/11			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0032794	PMID:39471804	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0011463	PMID:39471804	PCS		1/7			C	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000316	PMID:39471804	PCS		4/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001647	PMID:39471804	PCS		1/3			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0025336	PMID:39471804	PCS		10/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000278	PMID:39471804	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001007	PMID:39471804	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001249	PMID:39471804	PCS		14/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001265	PMID:39471804	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000574	PMID:39471804	PCS		3/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0011968	PMID:39471804	PCS		7/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001263	PMID:39471804	PCS		11/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0030948	PMID:39471804	PCS		3/11			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0031910	PMID:39471804	PCS		0/6			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0012385	PMID:39471804	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002908	PMID:39471804	PCS		4/11			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0011451	PMID:39471804	PCS		1/4			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000729	PMID:39471804	PCS		2/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000601	PMID:39471804	PCS		5/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0003316	PMID:39471804	PCS		0/3			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000325	PMID:39471804	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0008947	PMID:39471804	PCS		1/9			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002169	PMID:39471804	PCS		1/1			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000384	PMID:39471804	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0030674	PMID:39471804	PCS		1/7			C	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001508	PMID:39471804	PCS		2/2			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000817	PMID:39471804	PCS		1/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000414	PMID:39471804	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0009765	PMID:39471804	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001347	PMID:39471804	PCS		0/7			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000154	PMID:39471804	PCS		0/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001363	PMID:39471804	PCS		1/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0031936	PMID:39471804	PCS		11/12			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002570	PMID:39471804	PCS		1/10			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001081	PMID:39471804	PCS		4/13			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0001518	PMID:39471804	PCS		3/5			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000307	PMID:39471804	PCS		2/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0002205	PMID:39471804	PCS		1/8			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000664	PMID:39471804	PCS		2/3			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000028	PMID:39471804	PCS		2/7			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:621016	Neurodevelopmental disorder with variable familial hypercholanemia		HP:0000303	PMID:39471804	PCS		3/14			P	ORCID:0000-0002-0736-9199[2025-09-23]
OMIM:122750	Coxa vara		HP:0002812	OMIM:122750	IEA					P	HPO:iea[2009-02-17]
OMIM:122750	Coxa vara		HP:0000006	OMIM:122750	IEA					I	HPO:iea[2009-02-17]
OMIM:234820	Hemangiopericytoma, malignant		HP:0000007	OMIM:234820	IEA					I	HPO:iea[2009-02-17]
OMIM:234820	Hemangiopericytoma, malignant		HP:0001626	OMIM:234820	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0004599	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0002983	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0001561	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0003577	OMIM:600972	TAS					C	HPO:probinson[2022-05-06]
OMIM:600972	Achondrogenesis, type IB		HP:0000023	OMIM:600972	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0000272	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0003270	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0002093	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0012368	OMIM:600972	TAS					P	HPO:skoehler[2013-10-22]
OMIM:600972	Achondrogenesis, type IB		HP:0000969	OMIM:600972	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600972	Achondrogenesis, type IB		HP:0000946	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0003826	OMIM:600972	IEA					C	HPO:skoehler[2010-06-20]
OMIM:600972	Achondrogenesis, type IB		HP:0001537	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0000007	PMID:8528239	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-06]
OMIM:600972	Achondrogenesis, type IB		HP:0001789	OMIM:600972	TAS					P	HPO:skoehler[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0000774	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0008921	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:600972	Achondrogenesis, type IB		HP:0000773	OMIM:600972	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600972	Achondrogenesis, type IB		HP:0001623	OMIM:600972	IEA					P	HPO:iea[2009-02-17]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0001254	PMID:29917077	PCS		2/4			P	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0002067	PMID:29917077	PCS		1/4			P	HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0002376	PMID:29917077	PCS		4/4			P	HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0003819	PMID:29917077	PCS					C	HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0001639	PMID:29917077	PCS		1/4			P	HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0001251	PMID:29917077	IEA		3/4			P	HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0002072	PMID:29917077	PCS		2/4			P	HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0000602	PMID:29917077	PCS		2/4			P	HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0000007	PMID:29917077	PCS					I	HPO:probinson[2020-07-14];HPO:probinson[2020-07-14]
OMIM:618683	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6		HP:0001347	PMID:29917077	PCS		1/4			P	HPO:probinson[2020-07-14]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0003037	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0003015	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0003577	PMID:7859284	PCS		3/3			C	HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000463	PMID:7859284	PCS		3/3			P	HPO:iea[2018-03-07];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0004322	PMID:7859284	PCS		3/3			P	HPO:iea[2018-03-07];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0001371	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0010047	PMID:7859284	PCS		3/3			P	HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0002938	PMID:7859284	PCS		3/3			P	HPO:iea[2018-03-07];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000414	OMIM:215150	TAS					P	HPO:probinson[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0006532	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0002656	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000410	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0006237	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0004679	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0009803	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000336	PMID:7859284	PCS		3/3			P	HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0003026	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000175	PMID:7859284	PCS		0/3			P	HPO:probinson[2018-03-07];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0004279	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0005003	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0003088	PMID:7859284	PCS		3/3			P	HPO:iea[2018-03-07];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000272	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0011800	PMID:7859284	PCS		3/3			P	HPO:skoehler[2018-03-07];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0005280	PMID:7859284	PCS		3/3			P	HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0002829	OMIM:215150	TAS					P	HPO:skoehler[2014-02-06]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000407	PMID:7859284	PCS		3/3			P	HPO:skoehler[2014-05-04];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000926	OMIM:215150	TAS	HP:0011463				P	HPO:probinson[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000007	PMID:7859284	PCS					I	HPO:probinson[2018-03-07];HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0003417	OMIM:215150	TAS	HP:0011463				P	HPO:probinson[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000201	OMIM:215150	TAS					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000520	PMID:7859284	PCS		3/3			P	HPO:probinson[2022-12-10]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0000347	OMIM:215150	IEA					P	HPO:iea[2018-03-07]
OMIM:215150	Otospondylomegaepiphyseal dysplasia		HP:0004568	OMIM:215150	TAS					P	HPO:probinson[2016-07-08]
OMIM:621002	Premature ovarian failure 25		HP:0002960	PMID:35285020	PCS		0/2			P	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:621002	Premature ovarian failure 25		HP:0008209	PMID:35285020	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:621002	Premature ovarian failure 25		HP:0000858	PMID:35285020	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:621002	Premature ovarian failure 25		HP:0008222	PMID:35285020	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:621002	Premature ovarian failure 25		HP:0011462	PMID:35285020	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:621002	Premature ovarian failure 25		HP:0008232	PMID:35285020	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:621002	Premature ovarian failure 25		HP:0000007	PMID:35285020	PCS					I	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:621002	Premature ovarian failure 25		HP:0031103	PMID:35285020	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-12-26]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0002312	PMID:21419380	PCS		6/18		HP:0012825	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0003577	PMID:21419380	PCS		1/18			C	HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0001344	PMID:21419380	PCS		1/18			P	HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0000750	PMID:21419380	PCS		10/18			P	HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0001355	PMID:21419380	PCS		18/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0001250	PMID:21419380	PCS		1/18			P	HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0001252	PMID:21419380	PCS		7/18		HP:0012825	P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0003593	PMID:21419380	PCS		17/18			C	HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0001270	PMID:21419380	PCS		11/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0007341	PMID:21419380	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0007204	PMID:21419380	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0000256	PMID:21419380	PCS		18/18			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0000006	PMID:21419380	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-07]
OMIM:613926	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without impaired intellectual development		HP:0001249	PMID:21419380	PCS		5/18			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-03-07]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000286	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0002983	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000882	OMIM:614091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0002089	OMIM:614091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000200	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000089	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0001156	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0004322	OMIM:614091	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0002164	OMIM:614091	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0001395	OMIM:614091	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0010442	PMID:21473986	PCS					P	HPO:probinson[2013-02-23]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0008070	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0100840	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0009882	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0001789	OMIM:614091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000218	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000774	PMID:21473986	PCS					P	HPO:probinson[2013-02-23]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000773	PMID:21473986	PCS					P	HPO:probinson[2013-02-23]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000113	OMIM:614091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000476	OMIM:614091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0003026	OMIM:614091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0003027	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0002213	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000175	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0001541	OMIM:614091	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000691	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0010812	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0003180	OMIM:614091	IEA					P	HPO:skoehler[2019-04-18]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0100259	OMIM:614091	TAS					P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000107	PMID:21473986	PCS					P	HPO:probinson[2013-02-23]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000007	PMID:21473986	PCS					I	HPO:probinson[2013-01-09]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0006487	PMID:21473986	PCS					P	HPO:probinson[2013-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0001159	PMID:21473986	PCS					P	HPO:probinson[2013-02-23]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000268	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0000047	OMIM:614091	TAS				HP:0012825	P	HPO:skoehler[2014-02-25]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0006644	OMIM:614091	TAS					P	HPO:skoehler[2015-01-21]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0011090	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614091	Short-Rib thoracic dysplasia 7 with or without polydactyly		HP:0006349	OMIM:614091	IEA					P	HPO:skoehler[2018-10-08]
OMIM:210000	Behr syndrome		HP:0001771	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0003676	PMID:25012220	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0001310	PMID:25012220	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0001272	PMID:25012220	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0003593	PMID:25012220	PCS		1/6			C	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0001251	PMID:25012220	PCS		6/6			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0003390	PMID:25012220	PCS		2/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0001270	OMIM:210000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210000	Behr syndrome		HP:0007141	PMID:25012220	PCS		1/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0000639	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0011463	PMID:25012220	PCS		5/6			C	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0012450	PMID:25012220	PCS		3/6			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0000618	PMID:25012220	PCS		1/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0006970	PMID:25012220	PCS		1/5			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0002317	PMID:25012220	PCS		1/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0002359	PMID:25012220	PCS		1/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0001249	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0001347	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0006855	PMID:25012220	PCS		2/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0002015	PMID:25012220	PCS		2/6			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0002078	PMID:25012220	PCS		1/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0001288	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0003487	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0003089	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0001260	PMID:25012220	PCS		1/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0002191	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0000529	OMIM:210000	TAS					P	HPO:skoehler[2017-07-13]
OMIM:210000	Behr syndrome		HP:0034311	PMID:25012220	PCS		1/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0009830	PMID:25012220	PCS		4/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0000007	PMID:25012220	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0000505	PMID:25012220	PCS		2/4			P	HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0000648	PMID:25012220	PCS		6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-11-25]
OMIM:210000	Behr syndrome		HP:0006366	OMIM:210000	IEA					P	HPO:iea[2009-02-17]
OMIM:210000	Behr syndrome		HP:0001337	PMID:25012220	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-11-25]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000175	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0007429	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000252	PMID:28553959	PCS		3/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0004322	PMID:28553959	PCS		1/1			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0001250	PMID:28553959	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000490	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0001263	PMID:28553959	PCS		2/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000085	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0003593	PMID:28553959	PCS		3/6			C	HPO:probinson[2022-11-27];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000639	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0011463	PMID:28553959	PCS		3/6			C	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0002804	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000007	PMID:28553959	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0200024	PMID:28553959	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000444	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0002667	PMID:28553959	PCS		6/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000510	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0001510	PMID:28553959	PCS		2/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-27]
OMIM:617598	Mosaic variegated aneuploidy syndrome 3		HP:0000369	PMID:28553959	PCS		1/6			P	HPO:probinson[2022-11-27]
OMIM:618873	Lissencephaly 10		HP:0002069	PMID:32097630	PCS		2/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0002384	PMID:32097630	PCS		6/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0002121	PMID:32097630	PCS		1/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0032794	PMID:32097630	PCS		2/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0031882	PMID:32097630	PCS		2/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0032411	PMID:32097630	PCS		9/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0031589	PMID:32097630	PCS		2/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0000716	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0100704	PMID:32097630	PCS		2/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0000718	PMID:32097630	PCS		2/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0007302	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0001302	PMID:32097630	PCS		3/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0001249	PMID:32097630	PCS		6/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0000473	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0002353	PMID:32097630	PCS		11/11			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0002373	PMID:32097630	PCS		2/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0002197	PMID:32097630	PCS		2/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0010819	PMID:32097630	PCS		4/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0030222	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0001263	PMID:32097630	PCS		5/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0040196	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0007270	PMID:32097630	PCS		1/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0032792	PMID:32097630	PCS		3/12			P	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0000729	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0000668	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0007334	PMID:32097630	PCS		1/12			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0008765	PMID:32097630	PCS		1/13			P	HPO:probinson[2020-07-06]
OMIM:618873	Lissencephaly 10		HP:0000006	PMID:32097630	PCS					I	HPO:probinson[2020-07-06];HPO:probinson[2020-07-06]
OMIM:301119	Spermatogenic failure, X-linked, 8, susceptibility to		HP:0034011	PMID:38013430;PMID:38573307	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:301119	Spermatogenic failure, X-linked, 8, susceptibility to		HP:0032560	PMID:38013430	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:301119	Spermatogenic failure, X-linked, 8, susceptibility to		HP:0003251	PMID:38013430;PMID:38573307	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:301119	Spermatogenic failure, X-linked, 8, susceptibility to		HP:0011462	PMID:38013430;PMID:38573307	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:301119	Spermatogenic failure, X-linked, 8, susceptibility to		HP:0001417	PMID:38013430	PCS					I	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:301119	Spermatogenic failure, X-linked, 8, susceptibility to		HP:0000798	PMID:38013430;PMID:38573307	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:301119	Spermatogenic failure, X-linked, 8, susceptibility to		HP:0012865	PMID:38013430;PMID:38573307	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-08-05]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0000154	OMIM:309545	PCS					P	HPO:iea[2012-03-17];HP:probinson[2019-01-04]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0000321	OMIM:309545	IEA					P	HPO:iea[2009-02-17]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0000750	OMIM:309545	PCS					P	HPO:iea[2012-03-17];HP:probinson[2019-01-04]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0001250	OMIM:309545	IEA					P	HPO:iea[2009-02-17]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0002381	OMIM:309545	IEA					P	HPO:iea[2009-02-17]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0002719	OMIM:309545	IEA					P	HPO:iea[2009-02-17]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0008897	OMIM:309545	PCS					P	HPO:iea[2012-03-17];HP:probinson[2019-01-04]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0001417	OMIM:309545	IEA					I	HPO:iea[2009-02-17]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0000179	OMIM:309545	PCS					P	HPO:iea[2012-03-17];HP:probinson[2019-01-04]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0000248	OMIM:309545	IEA					P	HPO:iea[2009-02-17]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0000303	OMIM:309545	IEA					P	HPO:iea[2009-02-17]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0000215	OMIM:309545	PCS					P	HPO:iea[2012-03-17];HP:probinson[2019-01-04]
OMIM:309545	Intellectual developmental disorder, X-linked syndromic 12		HP:0001249	OMIM:309545	TAS					P	HPO:skoehler[2012-10-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0006824	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0005599	PMID:28183707;PMID:10349196	PCS		8/8			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-11-11];HPO:probinson[2022-03-14]
OMIM:214500	Chediak-Higashi syndrome		HP:0000486	PMID:23049325	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001250	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0001010	PMID:28183707	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:214500	Chediak-Higashi syndrome		HP:0002240	PMID:23049325	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0003593	PMID:26944273;PMID:10349196	PCS		14/19			C	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001251	PMID:20301751	PCS					P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0005592	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0032499	PMID:28183707;PMID:6243205	PCS		11/11			P	HPO:probinson[2020-11-06];HPO:probinson[2022-03-14]
OMIM:214500	Chediak-Higashi syndrome		HP:0002180	PMID:20301751	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0011993	PMID:20301751	PCS					P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0012156	PMID:29939658	PCS					P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0000639	PMID:20301751	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0002719	PMID:10349196	PCS		6/7			P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001903	PMID:29939658;PMID:28183707	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11];HPO:probinson[2022-03-14]
OMIM:214500	Chediak-Higashi syndrome		HP:0011462	PMID:26944273	PCS		4/9			C	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0009027	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0000613	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0002716	PMID:29939658	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0007663	PMID:26944273	PCS		2/9			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001107	PMID:26944273	PCS		8/9			P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0002218	PMID:23049325	PCS		4/4			P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0000978	PMID:29939658	PCS					P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001104	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0001324	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0005429	PMID:29939658	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0005406	PMID:23049325	PCS		3/4			P	HPO:probinson[2012-06-22];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001249	PMID:20301751	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0000952	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0001744	PMID:23049325	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0003623	PMID:26944273	PCS		1/9			C	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001265	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0000230	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0001288	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0001882	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0012484	PMID:20301751	PCS					P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0000704	PMID:29939658	PCS					P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0007133	PMID:29939658	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0000007	PMID:9215680	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0007730	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0004406	PMID:29939658	PCS					P	HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0000762	OMIM:214500	IEA					P	HPO:iea[2009-02-17]
OMIM:214500	Chediak-Higashi syndrome		HP:0001873	PMID:29939658	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001337	PMID:20301751	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-11]
OMIM:214500	Chediak-Higashi syndrome		HP:0001875	PMID:20301751	PCS					P	HPO:probinson[2020-11-11]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003202	PMID:37339631	PCS		5/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003698	PMID:37339631	PCS		1/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0002015	PMID:37339631	PCS		3/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003596	PMID:37339631	PCS		8/10			C	HPO:probinson[2024-03-10];HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0001288	PMID:37339631	PCS		2/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003487	PMID:37339631	PCS		1/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003484	PMID:37339631	PCS		2/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003551	PMID:37339631	PCS		4/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0001260	PMID:37339631	PCS		3/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0002380	PMID:37339631	PCS		2/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0033685	PMID:37339631	PCS		3/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0010875	PMID:37339631	PCS		1/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0007340	PMID:37339631	PCS		8/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003805	PMID:37339631	PCS		1/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0002878	PMID:37339631	PCS		1/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0025710	PMID:37339631	PCS		2/10			C	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0001324	PMID:37339631	PCS		1/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0000006	PMID:37339631	PCS					I	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0001315	PMID:37339631	PCS		5/10			P	HPO:probinson[2024-03-10]
OMIM:620452	Amyotrophic lateral sclerosis 28		HP:0003326	PMID:37339631	PCS		1/10			P	HPO:probinson[2024-03-10]
OMIM:605822	Spondyloocular syndrome		HP:0004325	OMIM:605822	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:605822	Spondyloocular syndrome		HP:0000164	PMID:26027496	PCS		0/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0003577	PMID:26027496	PCS		2/2			C	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0031846	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000541	PMID:26027496	PCS		2/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0004322	OMIM:605822	TAS		HP:0040283			P	HPO:skoehler[2015-08-16]
OMIM:605822	Spondyloocular syndrome		HP:0002162	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0005176	PMID:26027496	PCS		2/2			P	HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0012741	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000518	PMID:26027496	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000639	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000914	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000938	OMIM:605822	TAS					P	HPO:skoehler[2015-08-16]
OMIM:605822	Spondyloocular syndrome		HP:0001845	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0100807	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0002317	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0001324	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0007787	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0002953	PMID:26027496	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0001004	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0001763	PMID:26027496	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000358	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0002753	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0001166	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000591	PMID:26027496	PCS		0/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0010511	OMIM:605822	TAS					P	HPO:skoehler[2015-08-16]
OMIM:605822	Spondyloocular syndrome		HP:0000407	PMID:26027496	PCS		3/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000926	PMID:26027496	PCS		2/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000646	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000007	PMID:26027496	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000505	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000768	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0001631	PMID:26027496	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000465	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0002588	PMID:26027496	PCS		1/2			P	HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0000369	PMID:26027496	PCS		1/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:605822	Spondyloocular syndrome		HP:0001634	PMID:26027496	PCS		2/2			P	HPO:skoehler[2015-08-16];HPO:probinson[2022-12-14]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0003236	OMIM:254130	TAS					P	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0003693	OMIM:254130	TAS					P	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0003551	OMIM:254130	TAS					P	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0003581	OMIM:254130	TAS		HP:0040282			C	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0003560	OMIM:254130	IEA					P	HPO:iea[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0002460	OMIM:254130	TAS					P	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0003791	OMIM:254130	TAS		HP:0040283			P	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0009072	OMIM:254130	TAS					P	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0010546	OMIM:254130	TAS					P	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0007340	OMIM:254130	TAS					P	HPO:skoehler[2012-10-17]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0000007	OMIM:254130	TAS					I	HPO:probinson[2018-03-07]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0200101	OMIM:254130	TAS					P	HPO:skoehler[2013-06-05]
OMIM:254130	Miyoshi muscular dystrophy 1		HP:0030051	OMIM:254130	IEA					P	HPO:skoehler[2018-10-08]
OMIM:170980	Peroneal nerve, accessory deep		HP:0000707	OMIM:170980	IEA					P	HPO:iea[2009-02-17]
OMIM:170980	Peroneal nerve, accessory deep		HP:0000006	OMIM:170980	IEA					I	HPO:iea[2009-02-17]
OMIM:127600	Dyskeratosis, hereditary benign intraepithelial		HP:0000613	OMIM:127600	TAS		HP:0040283			P	HPO:skoehler[2013-06-06]
OMIM:127600	Dyskeratosis, hereditary benign intraepithelial		HP:0000505	OMIM:127600	IEA					P	HPO:iea[2009-02-17]
OMIM:127600	Dyskeratosis, hereditary benign intraepithelial		HP:0025337	OMIM:127600	IEA					P	HPO:skoehler[2018-10-08]
OMIM:127600	Dyskeratosis, hereditary benign intraepithelial		HP:0002745	OMIM:127600	IEA					P	HPO:iea[2009-02-17]
OMIM:127600	Dyskeratosis, hereditary benign intraepithelial		HP:0000006	OMIM:127600	IEA					I	HPO:iea[2009-02-17]
OMIM:620320	Hematuria, benign familial, 2		HP:0033282	PMID:11961012	PCS		0/4			P	HPO:probinson[2023-07-11]
OMIM:620320	Hematuria, benign familial, 2		HP:0003621	PMID:11961012	PCS		6/9			C	HPO:probinson[2023-07-11]
OMIM:620320	Hematuria, benign familial, 2		HP:0002907	PMID:11961012	PCS		9/9			P	HPO:probinson[2023-07-11]
OMIM:620320	Hematuria, benign familial, 2		HP:0000407	PMID:11961012	PCS		0/9			P	HPO:probinson[2023-07-11]
OMIM:620320	Hematuria, benign familial, 2		HP:0003581	PMID:11961012	PCS		3/9			C	HPO:probinson[2023-07-11]
OMIM:620320	Hematuria, benign familial, 2		HP:0000093	PMID:11961012	PCS		0/9			P	HPO:probinson[2023-07-11]
OMIM:620320	Hematuria, benign familial, 2		HP:0000006	PMID:11961012	PCS					I	HPO:probinson[2023-07-11]
OMIM:314500	Van den bosch syndrome		HP:0000970	OMIM:314500	IEA					P	HPO:iea[2009-02-17]
OMIM:314500	Van den bosch syndrome		HP:0000924	OMIM:314500	IEA					P	HPO:iea[2009-02-17]
OMIM:314500	Van den bosch syndrome		HP:0200016	OMIM:314500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:314500	Van den bosch syndrome		HP:0001417	OMIM:314500	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:314500	Van den bosch syndrome		HP:0001466	OMIM:314500	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:314500	Van den bosch syndrome		HP:0001139	OMIM:314500	IEA					P	HPO:iea[2009-02-17]
OMIM:314500	Van den bosch syndrome		HP:0001249	OMIM:314500	IEA					P	HPO:iea[2009-02-17]
OMIM:121270	Copper deficiency, familial benign		HP:0002212	OMIM:121270	TAS					P	HPO:probinson[2009-02-17]
OMIM:121270	Copper deficiency, familial benign		HP:0002234	OMIM:121270	TAS					P	HPO:probinson[2009-02-17]
OMIM:121270	Copper deficiency, familial benign		HP:0001250	OMIM:121270	IEA					P	HPO:iea[2009-02-17]
OMIM:121270	Copper deficiency, familial benign		HP:0001508	OMIM:121270	IEA					P	HPO:iea[2009-02-17]
OMIM:121270	Copper deficiency, familial benign		HP:0001051	OMIM:121270	IEA					P	HPO:iea[2009-02-17]
OMIM:121270	Copper deficiency, familial benign		HP:0001903	OMIM:121270	TAS				HP:0012825	P	HPO:nvasilevsky[2019-03-07]
OMIM:121270	Copper deficiency, familial benign		HP:0011967	OMIM:121270	TAS					P	HPO:probinson[2012-07-18]
OMIM:121270	Copper deficiency, familial benign		HP:0001417	OMIM:121270	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:121270	Copper deficiency, familial benign		HP:0000006	OMIM:121270	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0002333	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:6000461	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-04-03]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0002312	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0002015	PMID:37143309	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0031936	PMID:37143309	PCS		2/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0001332	PMID:37143309	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0001250	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0001260	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0002063	PMID:37143309	PCS		1/2			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0003593	PMID:37143309	PCS		3/3			C	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0002061	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0001270	PMID:37143309	PCS		2/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0002070	PMID:37143309	PCS		2/3			P	HPO:probinson[2024-03-02];HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0000716	PMID:37143309	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0000726	PMID:37143309	PCS	HP:0003621	3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0002505	PMID:37143309	PCS		2/2			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0000256	PMID:37143309	PCS	HP:0003593	3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0001257	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0000006	PMID:37143309	PCS					I	HPO:probinson[2024-03-02]
OMIM:620447	Megalencephalic leukoencephalopathy with subcortical cysts 3		HP:0006986	PMID:37143309	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0003233	PMID:21129723	PCS		6/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000882	PMID:21129723	PCS		1/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0004322	PMID:20534754	PCS		11/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001371	PMID:20534754	PCS		12/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001250	PMID:20534754	PCS		2/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0100490	OMIM:256040	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0003593	PMID:21881205	PCS		1/3			C	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0012785	PMID:21881205	PCS		3/3			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0011850	PMID:21953331	IEA		2/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0011463	PMID:21881205	IEA		2/3			C	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0033178	PMID:21129723	IEA		2/2			P	HPO:probinson[2020-10-12]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000998	PMID:21953331	PCS		5/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000953	OMIM:256040	TAS					P	HPO:skoehler[2012-11-18]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0100807	OMIM:256040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000956	PMID:21953331	PCS		2/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000158	PMID:21881205;PMID:20534754	PCS		5/15			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001324	OMIM:256040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002216	PMID:21129723	PCS		1/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001249	PMID:21881205	PCS		1/3			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0005328	PMID:21129723	PCS		1/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002215	PMID:21129723	PCS		2/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0003565	PMID:21881205;PMID:21953331;PMID:20534754	PCS		16/22			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0003202	PMID:21881205;PMID:21953331;PMID:21129723	PCS		12/24			P	HPO:probinson[2020-09-27];HPO:skoehler[2012-11-18];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0025131	PMID:21953331;OMIM:256040	PCS		17/19			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002155	PMID:21953331;PMID:20534754	PCS		6/21			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000771	PMID:21129723	PCS		1/6	MALE		P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0030783	PMID:21129723	PCS		2/2			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000292	PMID:21129723	PCS					P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0040270	PMID:21129723	PCS					P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0012219	PMID:21881205	PCS		3/3			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0100534	PMID:21953331	PCS		4/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002829	PMID:21953331	PCS		9/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000448	OMIM:256040	IEA					P	HPO:iea[2009-02-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000007	PMID:21129723	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000403	PMID:21953331	PCS		4/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001935	PMID:20534754	PCS		3/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0200035	PMID:21953331	PCS		9/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001538	PMID:21953331	PCS		7/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000400	OMIM:256040	IEA					P	HPO:iea[2009-02-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002788	PMID:21953331	PCS		1/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0008887	OMIM:256040	IEA					P	HPO:iea[2009-02-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002987	OMIM:256040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000520	PMID:21129723	PCS		1/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0003237	PMID:21881205	PCS		3/3			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0005830	OMIM:256040	TAS				HP:0012828	P	HPO:skoehler[2013-06-06]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0030356	PMID:21129723	PCS		2/2			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002240	PMID:21881205;PMID:21953331;PMID:20534754	PCS		19/24			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0011675	PMID:21881205	PCS		2/3			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0010783	OMIM:256040	IEA					P	HPO:skoehler[2010-06-20]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0010702	PMID:20534754	PCS		6/12			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001508	PMID:21953331;OMIM:256040	PCS		15/19			P	HPO:probinson[2020-09-27];HPO:skoehler[2012-10-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001507	OMIM:256040	IEA					P	HPO:iea[2009-02-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000858	PMID:21129723	PCS		1/6	FEMALE		P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0012450	PMID:21129723	PCS		2/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001822	PMID:21129723	PCS		2/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0009125	PMID:20534754	PCS	HP:0011463	12/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0009125	PMID:21881205	PCS		3/3			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0009125	PMID:21953331	PCS		9/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002716	PMID:21953331	PCS		7/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0012490	PMID:20534754	PCS					P	HPO:skoehler[2014-01-28];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002910	PMID:21953331	PCS		8/9			P	HPO:skoehler[2012-11-18];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000179	OMIM:256040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001744	PMID:21881205;PMID:21953331;PMID:20534754	PCS		10/24			P	HPO:probinson[2020-09-27];HPO:skoehler[2012-11-18];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002135	PMID:21881205;PMID:21953331;PMID:20534754	PCS		7/19			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002653	PMID:21129723	PCS		2/12			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001640	OMIM:256040	IEA					P	HPO:iea[2009-02-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000031	PMID:21953331	PCS		2/5	MALE		P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0003261	PMID:21881205	PCS		3/3			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0011421	PMID:21953331	PCS		1/9			C	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0011108	PMID:21953331	PCS		2/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0011227	PMID:21881205;PMID:21953331	PCS		12/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0100759	OMIM:256040	TAS					P	HPO:skoehler[2012-10-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0000509	PMID:21953331	PCS		4/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001635	OMIM:256040	IEA					P	HPO:iea[2009-02-17]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001954	PMID:21881205;PMID:21953331	PCS		12/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0030053	PMID:20534754	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0002925	PMID:21953331	PCS		2/9			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001510	PMID:21953331	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001873	PMID:21953331	PCS		1/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0001315	PMID:21129723	PCS		1/12			P	HPO:probinson[2020-09-27]
OMIM:256040	Proteasome-associated autoinflammatory syndrome 1 and digenic forms		HP:0007856	PMID:21129723	PCS		1/12			P	HPO:probinson[2020-09-27]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001254	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0000343	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001332	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0000463	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001250	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001252	PMID:9266390;OMIM:312170	PCS		11/12			P	HPO:probinson[2022-12-12];HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001274	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0003593	PMID:9266390	PCS		2/2			C	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001290	OMIM:312170	TAS					P	HPO:skoehler[2017-07-13]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002119	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002878	PMID:9266390	PCS		2/2			P	HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001423	PMID:9266390	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0000454	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001942	PMID:9266390	PCS		2/2			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001249	PMID:9266390	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0006799	OMIM:312170	TAS					P	HPO:skoehler[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0003128	PMID:9266390	PCS		2/2			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0003348	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002872	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0000252	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002059	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0000431	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0003542	PMID:9266390	PCS		1/1			P	HPO:probinson[2022-12-12];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001266	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0000496	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002131	OMIM:312170	TAS					P	HPO:skoehler[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002151	PMID:9266390	PCS		2/2			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001263	OMIM:312170	TAS					P	HPO:skoehler[2012-10-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002490	PMID:9266390	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002928	PMID:9266390	PCS		1/1			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001518	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0000508	OMIM:312170	IEA					P	HPO:skoehler[2010-06-20]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001999	OMIM:312170	IEA					P	HPO:skoehler[2010-06-20];HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0004925	OMIM:312170	TAS					P	HPO:skoehler[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0002007	OMIM:312170	IEA					P	HPO:iea[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0004900	OMIM:312170	TAS					P	HPO:skoehler[2009-02-17]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001337	PMID:9266390	PCS		1/2			P	HPO:probinson[2022-12-12]
OMIM:312170	Pyruvate dehydrogenase e1-alpha deficiency		HP:0001336	PMID:9266390	PCS		1/2			P	HPO:probinson[2022-12-12]
OMIM:613933	Acetyl-CoA carboxylase deficiency		HP:0003198	OMIM:613933	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613933	Acetyl-CoA carboxylase deficiency		HP:0001252	PMID:34552920	PCS		1/1			P	HPO:skoehler[2014-11-26]
OMIM:613933	Acetyl-CoA carboxylase deficiency		HP:0001263	PMID:34552920	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:613933	Acetyl-CoA carboxylase deficiency		HP:0002151	PMID:34552920	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:613933	Acetyl-CoA carboxylase deficiency		HP:6000430	PMID:34552920	PCS		1/1			P	HPO:probinson[2024-02-27]
OMIM:613933	Acetyl-CoA carboxylase deficiency		HP:0000007	PMID:34552920	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2024-02-27]
OMIM:613933	Acetyl-CoA carboxylase deficiency		HP:0001510	OMIM:613933	TAS					P	HPO:skoehler[2012-10-17]
OMIM:618866	Tremor, hereditary essential, 6		HP:0001272	PMID:31819945	PCS		0/1			P	HPO:probinson[2020-06-14];HPO:probinson[2024-03-16]
OMIM:618866	Tremor, hereditary essential, 6		HP:0003581	PMID:31819945	PCS					C	HPO:probinson[2024-03-16]
OMIM:618866	Tremor, hereditary essential, 6		HP:0002174	PMID:31819945	PCS	HP:0003581				P	HPO:probinson[2020-06-14]
OMIM:618866	Tremor, hereditary essential, 6		HP:0030186	PMID:31819945	PCS	HP:0003581				P	HPO:probinson[2020-06-14]
OMIM:618866	Tremor, hereditary essential, 6		HP:0012477	PMID:31819945	IEA	HP:0003581	24/197			P	HPO:probinson[2020-06-14]
OMIM:618866	Tremor, hereditary essential, 6		HP:0002415	PMID:31819945	PCS		0/1			P	HPO:probinson[2020-06-14];HPO:probinson[2024-03-16]
OMIM:618866	Tremor, hereditary essential, 6		HP:0000006	PMID:31819945	PCS					I	HPO:probinson[2020-06-14];HPO:probinson[2020-06-14]
OMIM:618866	Tremor, hereditary essential, 6		HP:0002346	PMID:31819945	PCS	HP:0003581	74/197			P	HPO:probinson[2020-06-14]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0001056	OMIM:131705	TAS					P	HPO:probinson[2009-02-17]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0001030	OMIM:131705	TAS					P	HPO:probinson[2009-02-17]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0008066	PMID:9406826	PCS	HP:0003623	6/6			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-09-30]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0001075	OMIM:131705	TAS				HP:0012825	P	HPO:probinson[2015-02-02]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0000007	OMIM:131705	TAS					I	HPO:probinson[2009-02-17]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0008404	OMIM:131705	TAS					P	HPO:skoehler[2013-05-03]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0000006	PMID:9406826	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2022-09-30]
OMIM:131705	Transient bullous dermolysis of the newborn		HP:0003623	PMID:9406826	PCS		6/6			C	HPO:probinson[2022-09-30]
OMIM:620321	C1q deficiency 2		HP:0007417	PMID:17513176;PMID:24160257	PCS		4/4			P	HPO:probinson[2023-06-18];HPO:probinson[2023-06-18];HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0002783	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0003493	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0025300	PMID:17513176	PCS		3/3			P	HPO:probinson[2023-06-18];HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0100750	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0011463	PMID:17513176;PMID:24160257	PCS		4/4			C	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0001903	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0100806	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0020102	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0001369	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0003565	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0000155	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0025434	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0001041	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0002110	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0200029	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0033399	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0033476	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0034601	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0011227	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0033040	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0002829	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0000007	PMID:24160257	PCS					I	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0000403	PMID:17513176	PCS		1/3			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0009710	PMID:24160257	PCS		1/1			P	HPO:probinson[2023-06-18]
OMIM:620321	C1q deficiency 2		HP:0002923	PMID:17513176;PMID:24160257	PCS		2/4			P	HPO:probinson[2023-06-18]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0003236	PMID:25125609	PCS		0/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0003676	PMID:25125609	PCS					C	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0003431	PMID:25125609	PCS		5/5			P	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0003596	PMID:25125609	PCS		3/5			C	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0001761	PMID:25125609	PCS		4/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0008959	PMID:25125609	PCS		4/5			P	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0006937	PMID:25125609	PCS		5/5			P	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0009053	PMID:25125609	PCS		4/5			P	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0011463	PMID:25125609	PCS		1/5			C	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0011462	PMID:25125609	PCS		1/5			C	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0009005	PMID:25125609	PCS		4/5			P	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0006886	PMID:25125609	PCS		5/5			P	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0003438	PMID:25125609	PCS		5/5			P	HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0000006	PMID:25125609	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:616687	Charcot-Marie-Tooth disease, axonal, type 2Y		HP:0001765	PMID:25125609	PCS		4/5			P	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-09]
OMIM:137360	GENOCHONDROMATOSIS		HP:0030298	PMID:17632779	PCS					P	HPO:lccarmody[2018-06-26]
OMIM:137360	GENOCHONDROMATOSIS		HP:0030295	PMID:17632779	PCS					P	HPO:lccarmody[2018-06-26]
OMIM:137360	GENOCHONDROMATOSIS		HP:0000006	PMID:17632779	PCS					I	HPO:iea[2009-02-17]
OMIM:233800	Grouped pigmentation of the macula		HP:0007703	OMIM:233800	TAS					P	HPO:probinson[2013-12-08]
OMIM:233800	Grouped pigmentation of the macula		HP:0012508	OMIM:233800	TAS					P	HPO:probinson[2013-12-14]
OMIM:233800	Grouped pigmentation of the macula		HP:0000007	OMIM:233800	TAS					I	HPO:probinson[2009-02-17]
OMIM:618872	Nizon-Isidor syndrome		HP:0001212	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000486	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000540	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000463	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0001250	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000160	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0001274	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0002020	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0001290	PMID:31155615	PCS		2/6			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0012724	PMID:31155615	PCS		3/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0001270	PMID:31155615	PCS		4/6			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0045075	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000718	PMID:31155615	PCS		4/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000739	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000316	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0008872	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000612	PMID:31155615	PCS		1/7		HP:0012833	P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0100807	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000414	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000219	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0007687	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0002714	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0002019	PMID:31155615	PCS		3/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0001763	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0001249	PMID:31155615	IEA		7/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000494	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000750	PMID:31155615	PCS		7/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0002079	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000232	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000194	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000490	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0005280	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000729	PMID:31155615	PCS		4/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000426	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0005619	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000348	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0002705	PMID:31155615	PCS		2/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000307	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0007018	PMID:31155615	PCS		3/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000047	PMID:31155615	PCS		1/4	MALE		P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000322	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000006	PMID:31155615	PCS					I	HPO:probinson[2020-06-27];HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000545	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:618872	Nizon-Isidor syndrome		HP:0000325	PMID:31155615	PCS		1/7			P	HPO:probinson[2020-06-27]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000286	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001374	OMIM:244450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000483	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000486	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0004322	OMIM:244450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000160	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0003196	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000482	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001252	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001290	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0004283	OMIM:244450	TAS					P	HPO:probinson[2012-07-15]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0045075	PMID:23200864	PCS		4/4			P	HPO:probinson[2022-05-07]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000639	OMIM:244450	IEA		4/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000319	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000954	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000316	PMID:23200864	PCS		3/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0006511	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001840	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0002019	PMID:23200864	PCS		2/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001601	OMIM:244450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000252	PMID:23200864	PCS					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001344	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0002079	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000007	PMID:23200864	PCS					I	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0004209	PMID:23200864	PCS		2/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000963	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000369	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000248	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000582	PMID:23200864	PCS		2/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000384	OMIM:244450	IEA		1/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0003577	PMID:23200864	PCS		4/4			C	HPO:probinson[2022-05-07]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000463	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001591	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000581	PMID:23200864	PCS		4/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001270	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0008070	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001629	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0002719	PMID:23200864	PCS		3/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001508	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0008872	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0002119	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000219	OMIM:244450	TAS		20/20			P	HPO:skoehler[2013-06-04];HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000218	PMID:23200864	PCS		1/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000059	OMIM:244450	IEA					P	HPO:skoehler[2019-04-18]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000377	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000699	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000275	OMIM:244450	IEA		2/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0008936	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000670	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0003300	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000276	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0003146	PMID:23200864	PCS		2/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001680	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0011302	OMIM:244450	TAS					P	HPO:probinson[2012-07-15]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0005280	PMID:23200864	PCS		4/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000506	PMID:23200864	PCS		4/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000508	PMID:23200864	PCS		3/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0008665	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000543	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0001631	PMID:23200864	PCS		2/4			P	HP:probinson[2018-04-16]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0002643	OMIM:244450	IEA		2/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000545	OMIM:244450	IEA					P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0000347	PMID:23200864	PCS		4/4			P	HPO:iea[2009-02-17]
OMIM:244450	Kaufman oculocerebrofacial syndrome		HP:0002566	OMIM:244450	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0002421	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0002521	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0002169	OMIM:617599	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0002540	OMIM:617599	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0001371	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0001250	OMIM:617599	IEA				HP:0031375	P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0003593	OMIM:617599	IEA					C	HPO:skoehler[2019-09-07]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0010841	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0100704	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0000817	PMID:28334793	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0001347	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0003623	OMIM:617599	IEA					C	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0008936	OMIM:617599	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0000252	OMIM:617599	IEA					P	HPO:skoehler[2019-04-18]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0001344	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0002079	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0011968	PMID:28334793	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0001382	OMIM:617599;PMID:28334793	TAS		20/20			P	HPO:nvasilevsky[2019-03-29];HPO:skoehler[2019-04-18]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0001263	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0040195	PMID:28334793	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0002509	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0000007	OMIM:617599	IEA					I	HPO:skoehler[2019-04-18]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0200134	OMIM:617599	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617599	Epileptic encephalopathy, early infantile, 55		HP:0001510	PMID:28334793	TAS					P	HPO:nvasilevsky[2019-03-29]
OMIM:614090	Sick sinus syndrome 3		HP:0011704	PMID:21378987	PCS					P	HPO:probinson[2022-07-09]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002113	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0010628	OMIM:612387	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002202	PMID:29299831	PCS		HP:0040284			P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002110	PMID:10430755	PCS		HP:0040283			P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0003581	PMID:10430755	PCS					C	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002240	OMIM:612387	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002097	PMID:10430755	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002094	OMIM:612387	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0012219	OMIM:612387	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002092	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0012418	PMID:10430755	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002091	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0032976	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0100721	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0006530	OMIM:612387	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0001217	PMID:10430755	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0100749	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0000554	OMIM:612387	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002206	PMID:29299831	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002107	PMID:10430755	PCS					P	HPO:probinson[2020-08-26]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0001744	OMIM:612387	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0000006	OMIM:612387	IEA					I	HPO:skoehler[2019-04-18]
OMIM:612387	Sarcoidosis, susceptibility to, 2		HP:0002105	PMID:10430755	IEA					P	HPO:probinson[2020-08-26]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0000473	PMID:33539324	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0002069	PMID:33539324	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0003621	PMID:33539324	PCS		3/3			C	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0000571	PMID:33539324	PCS		2/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0001310	PMID:33539324	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0001272	PMID:33539324	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0001260	PMID:33539324	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0002075	PMID:33539324	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0002061	PMID:33539324	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0012048	PMID:33539324	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0012049	PMID:33539324	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0002080	PMID:33539324	PCS		1/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0000514	PMID:33539324	PCS		2/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0000007	PMID:33539324	PCS					I	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0007325	PMID:33539324	PCS		3/3			P	HPO:probinson[2024-03-02]
OMIM:620453	Dystonia 22, juvenile-onset		HP:0001268	PMID:33539324	PCS	HP:0003581	3/3			P	HPO:probinson[2024-03-02]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001176	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001057	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002021	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0025267	PMID:38325380	PCS		2/17			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000085	PMID:38325380	PCS		2/17			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011410	PMID:38325380	PCS		9/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0012506	PMID:38325380	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0006191	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000518	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000639	PMID:38325380	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001845	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000998	PMID:38325380	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000637	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002019	PMID:38325380	PCS		4/16			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001840	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002138	PMID:38325380	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001187	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002035	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002033	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001182	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0100259	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000407	PMID:38325380	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000646	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000767	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000648	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000405	PMID:38325380	PCS		5/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000768	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000400	PMID:38325380	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002943	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000189	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002121	PMID:38325380	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000739	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0100702	PMID:38325380	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0006970	PMID:38325380	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001822	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0030084	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002015	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000750	PMID:38325380	PCS		16/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002013	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0025592	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011069	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000506	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000629	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000744	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000505	PMID:38325380	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002007	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0007018	PMID:38325380	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000501	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0004305	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001831	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000286	PMID:38325380	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000044	PMID:38325380	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001250	PMID:38325380	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001252	PMID:38325380	PCS		13/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001373	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000280	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0012028	PMID:38325380	PCS		1/16			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000716	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000718	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000717	PMID:38325380	PCS		9/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0008455	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000954	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000713	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000158	PMID:38325380	PCS		9/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000278	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002217	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001249	PMID:38325380	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002578	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003304	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0006934	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001385	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000175	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011968	PMID:38325380	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001382	PMID:38325380	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002591	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001263	PMID:38325380	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000294	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000609	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0009890	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000843	PMID:38325380	PCS		2/12			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001814	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000047	PMID:38325380	PCS		8/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000384	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001476	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000023	PMID:38325380	PCS		13/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000260	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000262	PMID:38325380	PCS		1/16			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0010862	PMID:38325380	PCS		16/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000938	PMID:38325380	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:6001070	PMID:38325380	PCS		0/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0009765	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000378	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000256	PMID:38325380	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000154	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000396	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000275	PMID:38325380	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003301	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002213	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003302	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000276	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000391	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000272	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0005280	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000822	PMID:38325380	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000821	PMID:38325380	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000823	PMID:38325380	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003416	PMID:38325380	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000028	PMID:38325380	PCS		5/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000121	PMID:38325380	PCS		2/17			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000483	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000486	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003072	PMID:38325380	PCS		1/11			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0010722	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0007443	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0009748	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000358	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002897	PMID:38325380	PCS		1/16			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003623	PMID:38325380	PCS		9/9			C	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001342	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003763	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002553	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000494	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011800	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011003	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000926	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001217	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0006101	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000369	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000126	PMID:38325380	PCS		2/17			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000341	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000582	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001792	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000343	PMID:38325380	PCS		7/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000581	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011599	PMID:38325380	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000337	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000219	PMID:38325380	PCS		12/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0100309	PMID:38325380	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000218	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000455	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0006335	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001562	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001561	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0003189	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000475	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002650	PMID:38325380	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001680	PMID:38325380	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011229	PMID:38325380	PCS		8/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011231	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000347	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002188	PMID:38325380	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001773	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000684	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0010808	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001097	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0004482	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000319	PMID:38325380	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0011220	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0031473	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001647	PMID:38325380	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002616	PMID:38325380	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000316	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000678	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001643	PMID:38325380	PCS		5/15			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002870	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000574	PMID:38325380	PCS		4/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002079	PMID:38325380	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002750	PMID:38325380	PCS		1/12			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000691	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0012532	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002190	PMID:38325380	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001537	PMID:38325380	PCS		9/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000448	PMID:38325380	PCS		0/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0030031	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0009931	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001417	PMID:36333996	PCS					I	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000201	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000541	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000540	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002286	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002162	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002280	PMID:38325380	PCS		0/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001629	PMID:38325380	PCS		2/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000656	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000414	PMID:38325380	PCS		3/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001622	PMID:38325380	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0002059	PMID:38325380	PCS		2/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001520	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0031936	PMID:38325380	PCS		15/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0100633	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0012520	PMID:38325380	PCS		1/13			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0100874	PMID:38325380	PCS		1/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000307	PMID:38325380	PCS		7/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000664	PMID:38325380	PCS		6/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0001631	PMID:38325380	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000787	PMID:38325380	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000303	PMID:38325380	PCS		2/18			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:301118	Intellectual developmental disorder, X-linked syndromic 37		HP:0000545	PMID:38325380	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-09-21]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0003202	OMIM:208100	IEA					P	HPO:skoehler[2019-04-18]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0003577	OMIM:208100	IEA					C	HPO:skoehler[2018-10-08]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0001762	OMIM:208100	IEA					P	HPO:skoehler[2019-04-18]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0003198	OMIM:208100	IEA					P	HPO:iea[2009-02-17]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0002803	OMIM:208100	IEA					P	HPO:skoehler[2010-06-18]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0000007	OMIM:208100	IEA					I	HPO:iea[2009-02-17]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0030680	OMIM:208100	IEA					P	HPO:iea[2009-02-17]
OMIM:208100	Arthrogryposis multiplex congenita, Neurogenic type		HP:0002804	OMIM:208100	TAS					P	HPO:probinson[2009-02-17]
OMIM:245000	Papillon-Lefevre syndrome		HP:0006308	OMIM:245000	IEA					P	HPO:iea[2009-02-17]
OMIM:245000	Papillon-Lefevre syndrome		HP:0000166	OMIM:245000	IEA	HP:0003593				P	HPO:iea[2009-02-17]
OMIM:245000	Papillon-Lefevre syndrome		HP:0006480	OMIM:245000	IEA					P	HPO:iea[2009-02-17]
OMIM:245000	Papillon-Lefevre syndrome		HP:0000007	PMID:10581027	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-24]
OMIM:245000	Papillon-Lefevre syndrome		HP:0006960	OMIM:245000	IEA					P	HPO:skoehler[2010-06-20]
OMIM:245000	Papillon-Lefevre syndrome		HP:0000972	OMIM:245000	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0000121	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0000164	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002983	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001250	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:6000873	OMIM:241500	TAS					P	HPO:probinson[2024-08-03]
OMIM:241500	Hypophosphatasia, infantile		HP:0005474	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001252	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0003491	OMIM:241500	TAS					P	HPO:probinson[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0003072	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001508	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001903	OMIM:241500	IEA					P	HPO:skoehler[2010-06-20]
OMIM:241500	Hypophosphatasia, infantile		HP:0000737	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002979	OMIM:241500	TAS					P	HPO:probinson[2012-05-28]
OMIM:241500	Hypophosphatasia, infantile		HP:0008873	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0003826	OMIM:241500	TAS					C	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001945	OMIM:241500	TAS					P	HPO:probinson[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002659	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001522	OMIM:241500	IEA					C	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002019	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0000773	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0000897	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002039	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0025430	OMIM:241500	TAS					P	HPO:probinson[2023-02-12];HPO:probinson[2023-02-12]
OMIM:241500	Hypophosphatasia, infantile		HP:0001363	OMIM:241500	TAS					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001561	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0001024	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002013	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0000592	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0003021	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0003282	PMID:3174660	PCS		1/1			P	HPO:probinson[2023-02-12]
OMIM:241500	Hypophosphatasia, infantile		HP:0002150	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0004492	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002170	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0011864	OMIM:241500	TAS					P	HPO:probinson[2012-05-28]
OMIM:241500	Hypophosphatasia, infantile		HP:0000926	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0006385	OMIM:241500	TAS					P	HPO:probinson[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0000007	PMID:3174660	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-12]
OMIM:241500	Hypophosphatasia, infantile		HP:0004606	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0003239	PMID:3174660;OMIM:241500	PCS		11/11			P	HPO:probinson[2023-02-12];HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002205	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0002104	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:241500	Hypophosphatasia, infantile		HP:0008428	OMIM:241500	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0000286	OMIM:190685	IEA		298/524			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0002023	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0004322	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0010808	PMID:15036797	PCS		157/524			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0001252	OMIM:190685	TAS		400/524			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0000639	PMID:15036797	PCS		17/524			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0000954	PMID:15036797;OMIM:190685	PCS		184/534			P	HPO:probinson[2022-05-15];HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0025656	PMID:31167209	PCS					P	HPO:probinson[2022-02-27]
OMIM:190685	Down syndrome		HP:0003745	OMIM:190685	IEA					I	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0000158	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0001643	PMID:15036797	PCS		11/58			P	HPO:probinson[2022-05-15];HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0001169	OMIM:190685	TAS					P	HPO:probinson[2013-04-07]
OMIM:190685	Down syndrome		HP:0001249	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0001382	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0010316	PMID:15036797	PCS		1/58			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0000405	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0001852	PMID:15036797	IEA		242/524			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0002866	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0000248	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0001655	PMID:15036797	PCS		5/58			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0000582	PMID:15036797	PCS		440/524			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0003577	PMID:15036797	PCS					C	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0001674	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0001156	PMID:15036797	PCS		58/524			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0004220	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0012368	OMIM:190685	TAS					P	HPO:skoehler[2014-11-27]
OMIM:190685	Down syndrome		HP:0001629	PMID:15036797	PCS		27/58			P	HPO:probinson[2022-05-15];HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0008551	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0100867	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0006695	PMID:15036797	PCS		2/58			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0030084	PMID:15036797	PCS		189/524			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0005989	PMID:15036797	PCS		193/524			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0002511	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0006733	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0004415	PMID:15036797	PCS		4/58			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0005547	OMIM:190685	IEA					P	HPO:skoehler[2015-01-21]
OMIM:190685	Down syndrome		HP:0001088	PMID:15036797	PCS		17/524			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0003467	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0004279	OMIM:190685	TAS					P	HPO:probinson[2013-04-07]
OMIM:190685	Down syndrome		HP:0000474	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0000272	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0002251	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0010773	PMID:15036797	PCS		1/58			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0003182	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0001719	PMID:15036797	PCS		2/58			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0001636	PMID:15036797	PCS		9/58			P	HPO:probinson[2022-05-15]
OMIM:190685	Down syndrome		HP:0000821	OMIM:190685	IEA					P	HPO:iea[2009-02-17]
OMIM:190685	Down syndrome		HP:0025705	PMID:34247811	PCS					P	HPO:probinson[2022-02-03]
OMIM:190685	Down syndrome		HP:0001631	PMID:15036797	PCS		17/58			P	HPO:probinson[2022-05-15];HPO:probinson[2022-05-15]
OMIM:619588	Epidermolysis bullosa simplex 2B, generalized intermediate		HP:0003577	PMID:1718160	PCS					C	HPO:probinson[2021-11-15]
OMIM:619588	Epidermolysis bullosa simplex 2B, generalized intermediate		HP:0007446	PMID:1718160	PCS		18/18			P	HPO:probinson[2021-11-15];HPO:probinson[2021-11-15]
OMIM:619588	Epidermolysis bullosa simplex 2B, generalized intermediate		HP:0000006	PMID:1718160	PCS					I	HPO:probinson[2021-11-15]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000486	PMID:26365382	PCS					P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000243	PMID:26365382	PCS		1/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0002186	PMID:26365382	PCS		3/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001250	PMID:26365382	PCS		5/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001252	PMID:26365382	PCS		4/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001290	OMIM:616863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000718	PMID:26365382	PCS		5/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000239	PMID:26365382	PCS		1/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001822	PMID:26365382	PCS		1/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001249	PMID:26365382	PCS		7/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000054	OMIM:616863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000750	PMID:26365382	PCS		6/6			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001344	OMIM:616863	IEA					P	HPO:skoehler[2018-10-08]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0030223	PMID:26365382	PCS					P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000270	PMID:26365382	PCS		1/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001263	PMID:26365382	PCS		7/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0010536	PMID:26365382	PCS					P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0012412	PMID:26365382	PCS		1/2			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000729	PMID:26365382	PCS		5/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0011098	OMIM:616863	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0001999	OMIM:616863	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0004209	PMID:26365382	PCS		1/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000028	PMID:26365382	PCS		3/4			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000369	PMID:26365382	PCS		1/7			P	HPO:probinson[2017-06-19]
OMIM:616863	Chromosome 16p13.2 deletion syndrome		HP:0000006	PMID:26365382	PCS					I	HPO:probinson[2017-06-19]
OMIM:308100	Ichthyosis, X-linked		HP:0007759	PMID:29672931	PCS		0/35			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0003577	PMID:29672931	PCS		15/35			C	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0003593	PMID:29672931	PCS		8/35			C	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0010788	PMID:3864567	PCS		2/76			P	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0008064	PMID:29672931	PCS		35/35			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0001419	PMID:3474618	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0011463	PMID:29672931	PCS		3/35			C	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0033252	PMID:29672931	PCS		5/35			P	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0007431	OMIM:308100	TAS					P	HPO:probinson[2009-02-17]
OMIM:308100	Ichthyosis, X-linked		HP:0000966	PMID:29672931	PCS		12/35			P	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0000982	PMID:29672931	PCS		3/35		HP:0012825	P	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0000028	PMID:29672931	PCS		4/35			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0001249	PMID:29672931	PCS		2/35			P	HPO:probinson[2022-05-04]
OMIM:308100	Ichthyosis, X-linked		HP:0003623	PMID:29672931	PCS		9/35			C	HPO:probinson[2022-05-04]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0008848	OMIM:612350	TAS					P	HPO:skoehler[2013-05-31]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0003015	PMID:31438591	PCS		4/6			P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000684	OMIM:612350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0006429	OMIM:612350	TAS					P	HPO:probinson[2012-06-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0004322	PMID:31438591	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0001073	PMID:31438591	PCS		5/7			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0100490	OMIM:612350	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0010049	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0003370	OMIM:612350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0003393	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0003071	OMIM:612350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0001270	PMID:31438591	PCS		3/6			P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0100864	OMIM:612350	TAS					P	HPO:probinson[2012-06-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000938	PMID:31438591	PCS		7/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000316	PMID:31438591	PCS		1/1			P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0002515	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000978	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000218	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0001763	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0009803	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000974	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0003301	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0002751	PMID:31438591	PCS		1/7			P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000494	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0001382	PMID:31438591	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000193	PMID:31438591	PCS		3/8			P	HPO:skoehler[2010-06-19];HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000592	PMID:31438591	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0001182	OMIM:612350	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0003083	PMID:31438591	PCS		3/6			P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0005280	PMID:31438591	PCS		1/1			P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0009473	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000926	PMID:31438591	PCS					P	HPO:skoehler[2010-06-19];HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000668	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000689	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000007	OMIM:612350	IEA					I	HPO:skoehler[2010-06-19]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0002007	PMID:31438591	PCS					P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0001015	OMIM:612350	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000465	PMID:31438591	PCS		8/8			P	HPO:probinson[2020-08-08]
OMIM:612350	Ehlers-Danlos syndrome, spondylodysplastic type, 3		HP:0000963	OMIM:612350	IEA					P	HPO:skoehler[2010-06-19]
OMIM:303900	Colorblindness, partial, protan series		HP:0200018	OMIM:303900	PCS					P	HPO:probinson[2012-04-06]
OMIM:303900	Colorblindness, partial, protan series		HP:0001419	OMIM:303900	PCS					I	HPO:probinson[2012-04-06]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0100950	OMIM:609016	TAS					P	HPO:probinson[2013-03-30]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0001252	OMIM:609016	TAS	HP:0003593				P	HPO:probinson[2013-03-30]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0002240	OMIM:609016	TAS	HP:0003593				P	HPO:probinson[2013-03-30]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0000580	OMIM:609016	TAS					P	HPO:probinson[2015-07-19]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0001943	OMIM:609016	TAS	HP:0003593				P	HPO:probinson[2013-01-09]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0000007	OMIM:609016	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0001638	OMIM:609016	TAS	HP:0003593				P	HPO:probinson[2013-03-30]
OMIM:609016	Long-Chain 3-hydroxyacyl-coa dehydrogenase deficiency		HP:0001699	OMIM:609016	TAS					P	HPO:probinson[2013-03-30]
OMIM:620484	Thrombocytopenia 10		HP:0000132	PMID:30591527	PCS		1/1			P	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0001892	PMID:30591527	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0003577	PMID:30591527	PCS		2/2			C	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0000007	PMID:30591527	PCS					I	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0000978	PMID:30591527	PCS		1/2			P	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0000967	PMID:30591527	PCS		1/2			P	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0004406	PMID:30591527	PCS		1/2			P	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0001873	PMID:30591527	PCS	HP:0003577	2/2			P	HPO:probinson[2024-02-11]
OMIM:620484	Thrombocytopenia 10		HP:0005537	PMID:30591527	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0001276	PMID:27799064	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000154	PMID:27799064	PCS		1/4			P	HPO:probinson[2023-06-09];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000252	PMID:27799064	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000463	PMID:27799064	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0011968	PMID:27799064	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0001250	PMID:27799064	PCS		3/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000490	PMID:27799064	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0001263	PMID:27799064	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0002151	PMID:27799064	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0001252	PMID:27799064	PCS		4/4			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0003593	PMID:27799064	PCS		4/4			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0030682	PMID:27799064	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0011800	PMID:27799064	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0005280	PMID:27799064	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000518	PMID:27799064	PCS		1/3			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0001508	PMID:27799064	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0001639	PMID:27799064	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0012240	PMID:27799064	PCS		3/3			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000007	PMID:27799064	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000414	PMID:27799064	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0000347	PMID:27799064	PCS		1/4			P	HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0003348	PMID:27799064	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0003128	PMID:27799064	PCS		4/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-06-09]
OMIM:617228	Combined oxidative phosphorylation deficiency 31		HP:0003557	PMID:27799064	PCS		2/3			P	HPO:probinson[2023-06-09]
OMIM:611881	Glycogen storage disease XII		HP:0000286	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0003236	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0003555	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0004322	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0003198	OMIM:611881	TAS		HP:0040283			P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0002162	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0001252	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0003593	PMID:8598869	PCS		1/1			C	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0002240	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:6000555	PMID:2825199	PCS		1/1			P	HPO:probinson[2024-04-03]
OMIM:611881	Glycogen storage disease XII		HP:0031964	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0001903	PMID:8598869	PCS	HP:0003593	1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0025435	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0001324	PMID:8598869	PCS	HP:0011463	1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0001249	OMIM:611881	TAS		HP:0040283			P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0000952	PMID:8598869	PCS	HP:0003593	1/1			P	HPO:probinson[2012-07-27];HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0001744	PMID:8598869	PCS		1/1			P	HPO:probinson[2012-07-27];HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0020181	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0003641	PMID:8598869	PCS		1/1		HP:0012825	P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0000470	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0001081	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0001082	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0002904	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0000508	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0000007	PMID:2825199	PCS					I	HPO:probinson[2012-07-27];HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0000823	OMIM:611881	TAS					P	HPO:probinson[2012-07-27]
OMIM:611881	Glycogen storage disease XII		HP:0001895	OMIM:611881	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611881	Glycogen storage disease XII		HP:0001930	OMIM:611881	TAS		1/1			P	HPO:probinson[2012-07-27];HPO:probinson[2022-10-01]
OMIM:611881	Glycogen storage disease XII		HP:0001897	OMIM:611881	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611881	Glycogen storage disease XII		HP:0003557	PMID:8598869	PCS		1/1			P	HPO:probinson[2022-10-01]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0003621	PMID:21092923	PCS		3/8			C	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0003596	PMID:21092923	PCS		1/8			C	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0002078	OMIM:613728	TAS					P	HPO:skoehler[2015-01-04]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0003487	PMID:21092923	PCS		2/8			P	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0001310	OMIM:613728	TAS					P	HPO:skoehler[2015-01-04]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0001761	PMID:21092923	PCS		3/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0001272	PMID:21092923	PCS		7/7		HP:0012828	P	HPO:skoehler[2013-06-06];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0001260	PMID:21092923	PCS		8/8			P	HPO:skoehler[2015-01-04];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0002066	PMID:21092923	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0002380	PMID:21092923	PCS		2/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0002070	PMID:21092923	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0033206	PMID:21092923	PCS		8/8			P	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0002080	OMIM:613728	TAS		HP:0040283			P	HPO:skoehler[2015-01-04]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0010545	PMID:21092923	PCS		3/8			P	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0007083	PMID:21092923	PCS		8/8			P	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0007350	PMID:21092923	PCS		8/8			P	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0000639	PMID:21092923	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0011462	PMID:21092923	PCS		4/8			C	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0000514	PMID:21092923	PCS		1/8			P	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0000503	PMID:21092923	PCS		3/8			P	HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0000007	PMID:21092923	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0007338	PMID:21092923	PCS		5/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-18]
OMIM:613728	Spinocerebellar ataxia, autosomal recessive 10		HP:0001249	PMID:21092923	PCS		2/8			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-04-18]
OMIM:266140	Pyropoikilocytosis, hereditary		HP:0004445	OMIM:266140	IEA					P	HPO:iea[2009-02-17]
OMIM:266140	Pyropoikilocytosis, hereditary		HP:0001878	OMIM:266140	IEA					P	HPO:iea[2009-02-17]
OMIM:266140	Pyropoikilocytosis, hereditary		HP:0004839	OMIM:266140	TAS					P	HPO:iea[2009-02-17]
OMIM:266140	Pyropoikilocytosis, hereditary		HP:0000007	OMIM:266140	IEA					I	HPO:iea[2009-02-17]
OMIM:266140	Pyropoikilocytosis, hereditary		HP:0004835	OMIM:266140	IEA					P	HPO:iea[2009-02-17]
OMIM:155240	Thyroid carcinoma, familial medullary		HP:0002865	OMIM:155240	IEA					P	HPO:iea[2009-02-17]
OMIM:155240	Thyroid carcinoma, familial medullary		HP:0000006	OMIM:155240	IEA					I	HPO:iea[2009-02-17]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0011463	PMID:16651346	PCS		1/1			C	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0030718	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0001723	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0031333	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0002615	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0012664	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0033568	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0000006	PMID:16651346	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0012249	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:612422	Cardiomyopathy, familial restrictive, 3		HP:0004942	PMID:16651346	PCS		1/1			P	HPO:probinson[2023-02-11]
OMIM:614053	Mitochondrial complex V (atp synthase) deficiency, nuclear type 3		HP:0001639	OMIM:614053	TAS					P	HPO:probinson[2013-08-10]
OMIM:614053	Mitochondrial complex V (atp synthase) deficiency, nuclear type 3		HP:0011925	PMID:20566710	PCS					P	HPO:probinson[2013-08-10]
OMIM:614053	Mitochondrial complex V (atp synthase) deficiency, nuclear type 3		HP:0009830	OMIM:614053	TAS					P	HPO:probinson[2013-08-10]
OMIM:614053	Mitochondrial complex V (atp synthase) deficiency, nuclear type 3		HP:0000007	PMID:20566710	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-24]
OMIM:614053	Mitochondrial complex V (atp synthase) deficiency, nuclear type 3		HP:0001249	OMIM:614053	TAS					P	HPO:probinson[2013-08-10]
OMIM:614053	Mitochondrial complex V (atp synthase) deficiency, nuclear type 3		HP:0003128	OMIM:614053	TAS	HP:0003623				P	HPO:probinson[2013-08-10]
OMIM:614053	Mitochondrial complex V (atp synthase) deficiency, nuclear type 3		HP:0003535	OMIM:614053	TAS					P	HPO:probinson[2013-08-10]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0003477	PMID:24468074	PCS		1/10			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000365	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0002067	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001310	PMID:24468074	PCS		2/10			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001332	PMID:24468074	PCS		1/10			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001250	PMID:24468074	PCS		1/10			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0002066	PMID:24468074;PMID:25056583	PCS		6/11			P	HPO:probinson[2022-03-08];HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001252	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0003593	PMID:24468074	PCS		3/10			C	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001251	PMID:25056583	PCS		1/1		HP:0025215	P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0031960	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000639	PMID:24468074	PCS		7/10		HP:0025215	P	HPO:iea[2009-02-17];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0011463	PMID:24468074;PMID:25056583	PCS		6/11			C	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000618	PMID:24468074	PCS		2/10			P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0006852	PMID:24468074	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001269	PMID:25056583	PCS		1/1			P	HPO:skoehler[2015-04-05];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001324	PMID:24468074	PCS		10/10		HP:0025215	P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0007965	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0002311	PMID:24468074;PMID:25056583	PCS		2/11			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-08];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000572	PMID:24468074	PCS				HP:0003676	P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0003621	PMID:24468074	PCS		2/10			C	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0002015	PMID:24468074;PMID:25056583	PCS		3/11			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0002078	PMID:24468074	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001761	PMID:24468074	PCS		3/10			P	HPO:skoehler[2009-02-17];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000012	PMID:24468074	PCS	HP:0011462	1/10			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0002131	PMID:24468074	PCS		10/10		HP:0025215	P	HPO:iea[2013-08-11];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001260	PMID:24468074;PMID:25056583	PCS		4/11			P	HPO:probinson[2022-03-08];HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001284	PMID:24468074;PMID:25056583	PCS		11/11			P	HPO:probinson[2022-03-08];HPO:iea[2009-02-17];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0004372	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0002172	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000408	PMID:24468074	PCS					P	HPO:skoehler[2015-01-04];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000529	PMID:24468074	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000407	PMID:24468074	PCS		10/10			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0001716	PMID:24468074	PCS		1/10			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000729	PMID:24468074	PCS		2/10			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000648	PMID:24468074;PMID:25056583	PCS		11/11			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-08];HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000505	PMID:25056583	PCS		1/1			P	HPO:probinson[2022-03-08]
OMIM:601338	Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss		HP:0000006	PMID:24468074	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-08]
OMIM:620490	Spermatogenic failure 85		HP:0032560	PMID:34172998	PCS		1/1			P	HPO:probinson[2024-02-11]
OMIM:620490	Spermatogenic failure 85		HP:0034011	PMID:34172998	PCS		1/1			P	HPO:probinson[2024-02-11]
OMIM:620490	Spermatogenic failure 85		HP:0003251	PMID:34172998	PCS		2/2			P	HPO:probinson[2024-02-11]
OMIM:620490	Spermatogenic failure 85		HP:0011462	PMID:34172998	PCS		2/2			C	HPO:probinson[2024-02-11]
OMIM:620490	Spermatogenic failure 85		HP:0000007	PMID:34172998	PCS					I	HPO:probinson[2024-02-11]
OMIM:620490	Spermatogenic failure 85		HP:0012869	PMID:34172998	PCS		1/1			P	HPO:probinson[2024-02-11]
OMIM:620490	Spermatogenic failure 85		HP:0012205	PMID:34172998	PCS		1/1			P	HPO:probinson[2024-02-11]
OMIM:611895	Amyotrophic lateral sclerosis 9		HP:0003693	PMID:17886298	PCS					P	HPO:probinson[2013-04-03]
OMIM:611895	Amyotrophic lateral sclerosis 9		HP:0002460	PMID:17886298	PCS					P	HPO:probinson[2013-04-03]
OMIM:611895	Amyotrophic lateral sclerosis 9		HP:0007354	OMIM:611895	TAS					P	HPO:skoehler[2015-01-19]
OMIM:611895	Amyotrophic lateral sclerosis 9		HP:0001257	PMID:17886298	PCS					P	HPO:probinson[2013-04-03]
OMIM:611895	Amyotrophic lateral sclerosis 9		HP:0000006	PMID:17886298	PCS					I	HPO:probinson[2013-04-03]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0001012	OMIM:600740	IEA					P	HPO:iea[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0002653	OMIM:600740	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0004398	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0000083	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0003072	OMIM:600740	IEA					P	HPO:iea[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0012378	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0000716	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0002918	OMIM:600740	IEA					P	HPO:iea[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0008200	OMIM:600740	IEA					P	HPO:skoehler[2010-06-20]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0003529	OMIM:600740	IEA					P	HPO:iea[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0002749	OMIM:600740	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0000934	OMIM:600740	IEA					P	HPO:iea[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0001324	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0002315	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0000787	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0001733	OMIM:600740	IEA					P	HPO:iea[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0003127	OMIM:600740	IEA					P	HPO:iea[2009-02-17]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0008659	OMIM:600740	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0000006	OMIM:600740	TAS					I	HPO:skoehler[2017-07-13]
OMIM:600740	Hypocalciuric hypercalcemia, familial, type III		HP:0002148	OMIM:600740	TAS					P	HPO:skoehler[2017-07-13]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0000176	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0000252	PMID:30311385	PCS		1/1			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0002521	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0000750	PMID:31696658;PMID:30311385;PMID:32341456	PCS		5/5			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0002188	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0031936	PMID:32341456	PCS		3/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0001250	PMID:32341456	PCS	HP:0003593	2/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0011968	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0000193	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0003593	PMID:32341456	PCS		3/3			C	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0010851	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0001270	PMID:31696658	PCS		1/1			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0012469	PMID:32341456	PCS		2/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0001508	PMID:30311385	PCS		1/1			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0000729	PMID:31696658	PCS		1/1			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0032792	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0009777	PMID:30311385	PCS		1/1			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0025336	PMID:32341456	PCS		3/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0000752	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0001631	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0001642	PMID:32341456	PCS		1/3			P	HPO:probinson[2021-05-11]
OMIM:619239	Neurodevelopmental disorder with or without autism or seizures		HP:0000006	PMID:32341456	PCS					I	HPO:probinson[2021-05-11]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0031507	PMID:1971148	PCS		3/3			P	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0011968	PMID:1971148	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0000260	PMID:1971148	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0001252	OMIM:275100	IEA					P	HPO:iea[2009-02-17]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0003593	PMID:1971148	PCS		3/3			C	HPO:probinson[2023-03-25];HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0001270	PMID:1971148	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0005280	PMID:1971148	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0000958	PMID:1971148	PCS		1/3			P	HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0031098	PMID:1971148	PCS		3/3			P	HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0001537	OMIM:275100	IEA					P	HPO:iea[2009-02-17]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0000007	PMID:1971148	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0000821	PMID:1971148	PCS		3/3			P	HPO:probinson[2023-03-25]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0008850	OMIM:275100	TAS					P	HPO:skoehler[2009-02-17]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0001539	PMID:1971148	PCS		1/3			P	HPO:iea[2009-02-17]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0001615	PMID:1971148	PCS		2/3			P	HPO:iea[2009-02-17]
OMIM:275100	Hypothyroidism, congenital, nongoitrous, 4		HP:0000158	PMID:1971148	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-25]
OMIM:617214	Spermatogenic failure 17		HP:0003251	PMID:26721930	PCS		2/2			P	HPO:probinson[2023-02-22]
OMIM:617214	Spermatogenic failure 17		HP:0011462	PMID:26721930	PCS		2/2			C	HPO:probinson[2023-02-22]
OMIM:617214	Spermatogenic failure 17		HP:0000007	PMID:26721930	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-22]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001177	PMID:17436244	PCS		3/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000486	PMID:17436244	PCS		1/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000365	PMID:17436244	PCS		1/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0004322	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000086	PMID:17436244	PCS		1/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000085	PMID:17436244	PCS		1/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000081	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000957	PMID:17436244	PCS		2/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000316	PMID:17436244	PCS		1/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000238	PMID:17436244	PCS		4/29			P	HPO:probinson[2020-11-28];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001643	PMID:17436244	PCS		4/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0009944	PMID:17436244	PCS		1/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0005528	PMID:17436244	PCS		25/28			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0009943	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001249	PMID:17436244	PCS		9/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000054	PMID:17436244	PCS		2/17	MALE		P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000252	PMID:17436244	PCS		25/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0002079	PMID:17436244	PCS		4/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0002032	PMID:17436244	PCS		1/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0010035	PMID:17436244	PCS		2/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000568	PMID:17436244	PCS		17/28			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000601	PMID:17436244	PCS		2/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000007	PMID:17436244	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001734	PMID:17436244	PCS		1/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0009777	PMID:17436244	PCS		3/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001896	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000125	PMID:17436244	PCS		4/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0009778	PMID:17436244	PCS		9/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000369	PMID:17436244	PCS		3/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001017	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0003213	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0003214	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000581	PMID:17436244	PCS		1/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001274	PMID:17436244	PCS		2/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001909	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000815	PMID:17436244	PCS		1/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001903	PMID:17436244	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000978	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001627	OMIM:227646	TAS					P	HPO:skoehler[2015-12-30]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0002575	PMID:17436244	PCS		1/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001000	PMID:17436244	PCS		19/29			P	HPO:skoehler[2014-03-24];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0003221	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000075	PMID:17436244	PCS		1/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001518	PMID:17436244	PCS	HP:0030674	24/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001873	PMID:17436244	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0007018	PMID:17436244	PCS		3/29			P	HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001876	PMID:17436244	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000028	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0003974	PMID:17436244	PCS		3/29			P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0000104	OMIM:227646	IEA					P	HPO:iea[2009-02-17]
OMIM:227646	Fanconi anemia, complementation group D2		HP:0001875	PMID:17436244	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-28]
OMIM:271400	Asplenia, isolated congenital		HP:0001894	OMIM:271400	TAS		HP:0040283			P	HPO:skoehler[2013-02-25]
OMIM:271400	Asplenia, isolated congenital		HP:0032550	PMID:12111187	PCS					P	HPO:probinson[2019-09-07]
OMIM:271400	Asplenia, isolated congenital		HP:0003593	OMIM:271400	TAS					C	HPO:skoehler[2012-10-17]
OMIM:271400	Asplenia, isolated congenital		HP:0001746	OMIM:271400	TAS					P	HPO:skoehler[2012-10-17]
OMIM:271400	Asplenia, isolated congenital		HP:0000006	OMIM:271400	TAS					I	HPO:skoehler[2012-10-17]
OMIM:618641	Infantile liver failure syndrome 3		HP:0001397	PMID:31204009	PCS		2/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0001396	PMID:31204009	PCS					P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0001762	PMID:31204009	IEA	HP:0003577	1/3			P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0004322	PMID:31204009	PCS					P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0003593	PMID:31204009	PCS					C	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0002240	PMID:31204009	PCS		3/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0002480	PMID:31204009	PCS					P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0003170	PMID:31204009	PCS		2/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0010574	PMID:31204009	PCS		3/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0012852	PMID:31204009	PCS		1/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0008151	PMID:31204009	PCS		3/3			P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0003819	PMID:31204009	PCS		1/3			C	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0000926	PMID:31204009	PCS		1/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0000007	PMID:31204009	PCS					I	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0001987	PMID:31204009	PCS					P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0008479	PMID:31204009	PCS		3/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0006554	PMID:31204009	PCS	HP:0003593				P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0002910	PMID:31204009	PCS					P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0000952	PMID:31204009	PCS					P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0001744	PMID:31204009	PCS		2/3			P	HPO:probinson[2020-07-07]
OMIM:618641	Infantile liver failure syndrome 3		HP:0004568	PMID:31204009	PCS		3/3			P	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0003621	PMID:28575650	PCS					C	HPO:probinson[2022-11-08]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0008052	PMID:28575650	PCS					P	HPO:probinson[2022-11-08]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0000541	PMID:28575650	PCS					P	HPO:probinson[2022-11-08]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0000639	PMID:28575650	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0011530	PMID:28575650	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0000546	PMID:28575650	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2022-11-08]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0030490	PMID:28575650	PCS					P	HPO:probinson[2022-11-08]
OMIM:617572	Exudative vitreoretinopathy 7		HP:0000006	PMID:28575650	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-08]
OMIM:610209	Migraine with or without aura, susceptibility to, 11		HP:0002013	OMIM:610209	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610209	Migraine with or without aura, susceptibility to, 11		HP:0002077	OMIM:610209	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610209	Migraine with or without aura, susceptibility to, 11		HP:0000613	OMIM:610209	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610209	Migraine with or without aura, susceptibility to, 11		HP:0002083	OMIM:610209	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610209	Migraine with or without aura, susceptibility to, 11		HP:0002183	OMIM:610209	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610209	Migraine with or without aura, susceptibility to, 11		HP:0002018	OMIM:610209	IEA					P	HPO:skoehler[2010-06-19]
OMIM:610209	Migraine with or without aura, susceptibility to, 11		HP:0000006	OMIM:610209	IEA					I	HPO:skoehler[2010-06-19]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0003236	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0001288	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0003693	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0002460	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0031237	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0009027	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0003805	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0003736	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0003803	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0003701	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0020203	PMID:30900782	PCS					P	HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0000006	PMID:30900782	PCS					I	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:618655	Myopathy, distal, 6, adult onset		HP:0003557	PMID:30900782	PCS					P	HPO:probinson[2020-06-23];HPO:probinson[2020-06-23]
OMIM:142700	Developmental dysplasia of the hip 1		HP:0001374	OMIM:142700	IEA					P	HPO:iea[2009-02-17]
OMIM:142700	Developmental dysplasia of the hip 1		HP:0008807	OMIM:142700	IEA					P	HPO:iea[2009-02-17]
OMIM:142700	Developmental dysplasia of the hip 1		HP:0001426	OMIM:142700	IEA					I	HPO:iea[2009-02-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0000121	PMID:2212001	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0002199	PMID:2212001	PCS		2/2			P	HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0031817	PMID:2212001	PCS		2/2			P	HPO:lccarmody[2018-09-25];HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0003593	PMID:2212001	PCS		2/2			C	HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0001281	PMID:2212001	PCS		1/2			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0000829	PMID:2212001	PCS		2/2			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-09-25];HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0000518	OMIM:146200	IEA					P	HPO:iea[2009-02-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0000737	PMID:2212001	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0031990	PMID:2212001	PCS		1/2			P	HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0002905	PMID:2212001	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0000007	OMIM:146200	IEA					I	HPO:skoehler[2019-09-07]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0025303	PMID:2212001	PCS		1/2			C	HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0002901	PMID:2212001	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0002514	OMIM:146200	IEA					P	HPO:iea[2009-02-17]
OMIM:146200	Hypoparathyroidism, familial isolated		HP:0000006	PMID:2212001	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-08-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0005216	PMID:9158151	PCS		1/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003554	OMIM:601462	IEA					P	HPO:iea[2009-02-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003596	PMID:9158151	PCS		1/4			C	HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003473	PMID:9158151	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003593	PMID:9158151	PCS		1/4			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0007340	PMID:9158151	PCS		1/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0000218	OMIM:601462	TAS		HP:0040283			P	HPO:skoehler[2015-04-26]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0008954	PMID:9158151	PCS		1/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0000597	OMIM:601462	IEA					P	HPO:iea[2009-02-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0002015	OMIM:601462	IEA					P	HPO:iea[2009-02-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003324	PMID:9158151	PCS		2/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003621	PMID:9158151	PCS		1/4			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003443	OMIM:601462	IEA					P	HPO:iea[2009-02-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0011968	OMIM:601462	TAS					P	HPO:skoehler[2015-04-26]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003484	PMID:9158151	PCS		4/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0001260	OMIM:601462	IEA					P	HPO:iea[2009-02-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0030208	PMID:9158151	PCS		0/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0025709	PMID:9158151	PCS		1/4			C	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0009130	PMID:9158151	PCS		3/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0009113	PMID:9158151	PCS		2/4			P	HPO:probinson[2022-09-04];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0000508	OMIM:601462	IEA					P	HPO:iea[2009-02-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0000602	OMIM:601462	TAS					P	HPO:skoehler[2015-04-26]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0004889	OMIM:601462	IEA					P	HPO:iea[2009-02-17]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0000006	PMID:9158151	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:601462	Myasthenic syndrome, congenital, 1A, slow-channel		HP:0003436	PMID:9158151	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-09-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0000819	PMID:14645853	PCS		1/13			P	HPO:skoehler[2010-06-18];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0003124	PMID:14645853	PCS		9/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0003581	PMID:14645853	PCS		13/13			C	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0000822	PMID:14645853	PCS		8/13			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0001658	PMID:14645853	PCS		9/13			P	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0100749	PMID:14645853	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0005181	PMID:14645853	PCS		13/13			P	HPO:probinson[2023-02-04];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0000006	PMID:14645853	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-04]
OMIM:608320	Coronary artery disease, autosomal dominant, 1		HP:0001513	PMID:14645853	PCS		1/13			P	HPO:probinson[2023-02-04]
OMIM:212400	Cataract and congenital ichthyosis		HP:0000518	OMIM:212400	IEA					P	HPO:iea[2009-02-17]
OMIM:212400	Cataract and congenital ichthyosis		HP:0007431	OMIM:212400	IEA					P	HPO:iea[2009-02-17]
OMIM:212400	Cataract and congenital ichthyosis		HP:0000007	OMIM:212400	IEA					I	HPO:iea[2009-02-17]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0001265	PMID:25818867	PCS		10/21			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0003401	PMID:25818867	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0003676	PMID:25818867	PCS					C	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0003596	PMID:25818867	PCS		6/18			C	HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0002495	PMID:25818867	PCS		12/21			P	HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0003584	PMID:25818867	PCS		8/18			C	HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0012514	PMID:25818867	PCS		20/20			P	HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0010871	PMID:25818867	PCS		9/21			P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0000639	PMID:25818867	PCS		0/17			P	HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0011462	PMID:25818867	PCS		4/18			C	HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0009830	PMID:25818867	PCS					P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0002936	PMID:25818867	PCS					P	HPO:skoehler[2015-08-02];HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0001324	PMID:25818867	PCS		0/21			P	HPO:probinson[2023-03-29]
OMIM:616491	Charcot-Marie-Tooth disease, axonal, type 2V		HP:0000006	PMID:25818867	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-03-29]
OMIM:265850	PYGMY		HP:0000818	OMIM:265850	IEA					P	HPO:iea[2009-02-17]
OMIM:265850	PYGMY		HP:0004322	OMIM:265850	TAS	HP:0003593				P	HPO:skoehler[2009-02-17]
OMIM:265850	PYGMY		HP:0001939	OMIM:265850	IEA					P	HPO:iea[2009-02-17]
OMIM:265850	PYGMY		HP:0000007	OMIM:265850	IEA					I	HPO:iea[2009-02-17]
OMIM:265850	PYGMY		HP:0001426	OMIM:265850	IEA					I	HPO:iea[2009-02-17]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0001265	PMID:27055475	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0004576	PMID:27055475	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0001250	OMIM:615198	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0003155	OMIM:615198	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0001263	PMID:27055475	PCS		1/1			P	HPO:skoehler[2013-05-03];HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0001252	PMID:27055475	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0003593	PMID:27055475	PCS		1/1			C	HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0100255	OMIM:615198	IEA					P	HPO:skoehler[2015-01-21]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0100923	OMIM:615198	TAS					P	HPO:skoehler[2014-04-04]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0001508	PMID:27055475	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0011001	PMID:27055475	PCS		0/1			P	HPO:skoehler[2013-05-30];HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0000007	PMID:27055475	PCS					I	HPO:skoehler[2013-05-03];HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0100959	PMID:27055475	PCS		1/1			P	HPO:probinson[2022-12-13]
OMIM:615198	Osteosclerotic metaphyseal dysplasia		HP:0001249	OMIM:615198	TAS		HP:0040283			P	HPO:skoehler[2013-11-18]
OMIM:614286	Myelodysplastic syndrome		HP:0001442	OMIM:614286	TAS					I	HPO:probinson[2013-08-10]
OMIM:614286	Myelodysplastic syndrome		HP:0002863	OMIM:614286	TAS					P	HPO:probinson[2013-01-09]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0002553	OMIM:216100	TAS					P	HPO:probinson[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0000252	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0003995	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0001377	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0004322	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0001780	OMIM:216100	TAS					P	HPO:probinson[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0000085	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0001191	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0000508	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0000316	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0001438	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0000007	OMIM:216100	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0000824	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0009601	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0000204	OMIM:216100	TAS					P	HPO:probinson[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0001249	OMIM:216100	IEA					P	HPO:iea[2009-02-17]
OMIM:216100	Cleft lip/palate with abnormal thumbs and microcephaly		HP:0001545	OMIM:216100	TAS					P	HPO:probinson[2012-03-02]
OMIM:611498	Nephronophthisis 7		HP:0003774	PMID:17618285	PCS					P	HPO:probinson[2013-02-22]
OMIM:611498	Nephronophthisis 7		HP:0000007	PMID:17618285	PCS					I	HPO:probinson[2013-01-09]
OMIM:611498	Nephronophthisis 7		HP:0000090	PMID:17618285	PCS					P	HPO:probinson[2013-02-22]
OMIM:611498	Nephronophthisis 7		HP:0000092	PMID:17618285	PCS					P	HPO:probinson[2013-02-22]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001276	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0007759	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000486	PMID:32302043	PCS		31/39			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0004322	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000463	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001596	PMID:32302043	PCS		56/56			P	HPO:skoehler[2010-06-20];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000260	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001250	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000262	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0003196	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001252	OMIM:601853	TAS					P	HPO:skoehler[2014-11-26]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001251	PMID:32302043	PCS		19/30			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001290	OMIM:601853	TAS					P	HPO:skoehler[2017-07-13]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0100543	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000716	OMIM:601853	IEA					P	HPO:skoehler[2018-10-08]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000319	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000316	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000218	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0007302	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0003745	OMIM:601853	IEA					I	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0002678	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000752	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000358	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0002335	OMIM:601853	TAS					P	HPO:probinson[2012-06-10]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001347	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0006899	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001320	OMIM:601853	TAS					P	HPO:probinson[2012-06-10]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0031912	PMID:32302043	PCS		29/44			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001363	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000494	PMID:32302043	PCS		20/25			P	HPO:probinson[2020-09-12];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000233	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0031913	PMID:32302043	PCS	HP:0030674	55/56			P	HPO:skoehler[2018-10-08];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0001263	PMID:32302043	IEA		31/43			P	HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000272	PMID:32302043	PCS		41/44			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0011800	OMIM:601853	TAS					P	HPO:skoehler[2013-11-28]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0100716	OMIM:601853	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000824	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0002645	OMIM:601853	IEA					P	HPO:iea[2009-02-17]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000369	PMID:32302043	PCS	HP:0003577	38/41			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:601853	Gomez-Lopez-Hernandez syndrome		HP:0000248	PMID:32302043	PCS		41/46			P	HPO:iea[2009-02-17];HPO:probinson[2020-09-12]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0002014	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0002630	OMIM:601847	TAS					P	HPO:probinson[2012-07-16]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0001046	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0004322	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0003155	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0001394	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0002240	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0003593	OMIM:601847	IEA					C	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0002908	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0001508	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0003819	OMIM:601847	IEA					C	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0000007	OMIM:601847	IEA					I	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0000989	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0001406	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0001744	OMIM:601847	IEA					P	HPO:iea[2009-02-17]
OMIM:601847	Cholestasis, progressive familial intrahepatic 2		HP:0001402	OMIM:601847	IEA					P	HPO:skoehler[2010-06-20]
OMIM:168300	Paramyotonia congenita		HP:0005348	OMIM:168300	TAS	HP:0003621				P	HPO:skoehler[2012-11-20]
OMIM:168300	Paramyotonia congenita		HP:0003552	OMIM:168300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:168300	Paramyotonia congenita		HP:0011809	OMIM:168300	TAS					P	HPO:probinson[2012-07-16]
OMIM:168300	Paramyotonia congenita		HP:0011968	OMIM:168300	TAS	HP:0011463				P	HPO:skoehler[2012-11-20]
OMIM:168300	Paramyotonia congenita		HP:0003593	OMIM:168300	IEA					C	HPO:skoehler[2009-02-17]
OMIM:168300	Paramyotonia congenita		HP:0012899	OMIM:168300	TAS					P	HPO:skoehler[2014-06-24]
OMIM:168300	Paramyotonia congenita		HP:0001319	OMIM:168300	IEA		HP:0040283			P	HPO:skoehler[2010-06-20]
OMIM:168300	Paramyotonia congenita		HP:0003712	OMIM:168300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:168300	Paramyotonia congenita		HP:0010548	OMIM:168300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:168300	Paramyotonia congenita		HP:0001324	OMIM:168300	TAS					P	HPO:skoehler[2012-11-20]
OMIM:168300	Paramyotonia congenita		HP:0000006	OMIM:168300	IEA					I	HPO:iea[2009-02-17]
OMIM:168300	Paramyotonia congenita		HP:0003326	OMIM:168300	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000187	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000486	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001795	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0004322	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001250	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001274	OMIM:300004	TAS		20/20			P	HPO:skoehler[2009-02-17];HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000280	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001090	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000639	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001845	OMIM:300004	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000218	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000411	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000336	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001007	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000110	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000252	OMIM:300004	TAS					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0002510	OMIM:300004	TAS					P	HPO:skoehler[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0002650	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0003121	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001263	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000294	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001182	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000505	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000648	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001319	OMIM:300004	IEA					P	HPO:skoehler[2010-06-18]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0001417	OMIM:300004	IEA					I	HPO:skoehler[2010-06-19]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000664	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000047	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0000028	OMIM:300004	IEA					P	HPO:iea[2009-02-17]
OMIM:300004	Corpus callosum, agenesis of, with abnormal genitalia		HP:0002445	OMIM:300004	IEA					P	HPO:skoehler[2010-06-20]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0000252	PMID:33500254	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0003621	PMID:33500254	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0002650	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0004322	PMID:33500254	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0001596	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0030344	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0001263	PMID:33500254	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0030341	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0034323	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0040075	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0011003	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0000815	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0000407	PMID:33500254	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0031098	PMID:33500254	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0011462	PMID:33500254	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0000007	PMID:33500254	PCS					I	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:620651	Diabetes, deafness, developmental delay, and short stature syndrome		HP:0005978	PMID:33500254	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:180870	Ruvalcaba syndrome		HP:0000252	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000494	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0002983	OMIM:180870	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180870	Ruvalcaba syndrome		HP:0001377	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0001773	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0002650	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0004279	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000023	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000430	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0004322	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000460	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0010049	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0010743	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0002808	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000678	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000769	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000823	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000774	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0200055	OMIM:180870	TAS					P	HPO:skoehler[2012-10-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000006	OMIM:180870	IEA					I	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000028	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0001249	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0009803	OMIM:180870	IEA					P	HPO:iea[2009-02-17]
OMIM:180870	Ruvalcaba syndrome		HP:0000556	OMIM:180870	TAS					P	HPO:probinson[2015-07-20]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0001132	PMID:21885030	PCS		3/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0100832	PMID:21885030	PCS		5/13			P	HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0200071	PMID:21885030	PCS		9/13			P	HPO:skoehler[2013-05-31];HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0000541	PMID:21885030	PCS		4/13			P	HPO:skoehler[2012-11-18];HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0000518	PMID:21885030	PCS		11/13			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0011463	PMID:21885030	PCS		13/13			C	HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0007992	PMID:21885030	PCS		3/13			P	HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0000007	PMID:21885030	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0032037	PMID:21885030	PCS	HP:0011463	13/13			P	HPO:probinson[2022-10-18]
OMIM:614292	Myopia, high, with cataract and vitreoretinal degeneration		HP:0011003	PMID:21885030	PCS	HP:0011463	9/11			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-10-18]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0002014	PMID:34750991	PCS		1/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0001289	PMID:34750991	PCS		2/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0002013	PMID:34750991	PCS		2/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0011924	PMID:34750991	PCS		2/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0002151	PMID:34750991	PCS		2/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0011463	PMID:34750991	PCS		2/2			C	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0008551	PMID:34750991	PCS		1/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0000007	PMID:34750991	PCS					I	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0001987	PMID:34750991	PCS		2/2			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0001943	PMID:34750991	PCS		2/2			P	HPO:probinson[2023-01-19];HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0001945	PMID:34750991	PCS		1/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0002788	PMID:34750991	PCS		1/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0001733	PMID:34750991	PCS		1/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0002027	PMID:34750991	PCS		1/2			P	HPO:probinson[2023-01-19]
OMIM:620137	Mitochondrial complex III deficiency, nuclear type 11		HP:0001942	PMID:34750991	PCS		2/2			P	HPO:probinson[2023-01-19]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0003016	OMIM:612813	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0003027	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0008905	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0001156	OMIM:612813	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0002651	OMIM:612813	IEA					P	HPO:skoehler[2015-01-27]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0001552	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0001382	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0000272	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0000470	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0005285	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0004482	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0011800	OMIM:612813	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0011304	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0009381	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0010582	OMIM:612813	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0001609	PMID:19110214	IEA		2/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0000926	OMIM:612813	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0002938	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0000007	PMID:19110214	IEA					I	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:4000007	OMIM:612813	IEA					P	HPO:skoehler[2019-04-18]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0000369	PMID:19110214	IEA		3/3		HP:0012825	P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0000303	PMID:19110214	IEA		3/3			P	HPO:probinson[2012-07-29]
OMIM:612813	Spondyloepimetaphyseal dysplasia, Aggrecan type		HP:0000358	PMID:19110214	IEA		3/3		HP:0012825	P	HPO:probinson[2012-07-29]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0004322	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0001250	PMID:30661771	PCS		4/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0001252	PMID:30661771	PCS		5/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0003593	PMID:30661771	PCS		5/5			C	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0011856	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000319	PMID:30661771	PCS		1/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0100602	PMID:30661771	PCS		1/5			H	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0002317	PMID:30661771	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000219	PMID:30661771	PCS		1/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000218	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0002019	PMID:30661771	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0001622	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0008936	PMID:30661771	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0001562	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0002353	PMID:30661771	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000750	PMID:30661771	PCS		5/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0031936	PMID:30661771	PCS		3/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000490	PMID:30661771	PCS		4/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0001263	PMID:30661771	PCS		5/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0410263	PMID:30661771	PCS		0/4			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0100023	PMID:30661771	PCS		3/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0100876	PMID:30661771	PCS		2/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0034210	PMID:30661771	PCS	HP:0034197	1/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0010880	PMID:30661771	PCS	HP:0034197	2/5			P	HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0002509	PMID:30661771	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000426	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000007	PMID:30661771	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0004209	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000960	PMID:30661771	PCS		2/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0001257	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:618480	Neurodevelopmental disorder with seizures and speech and walking impairment		HP:0000369	PMID:30661771	PCS		1/5			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-25]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0001596	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0001681	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0000272	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0040160	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0011800	OMIM:176670	TAS					P	HPO:skoehler[2013-11-28]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0005181	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0007485	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0001658	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0001635	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0000007	OMIM:176670	TAS					I	HPO:skoehler[2015-12-30];HP:probinson[2019-01-04]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0001510	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0004416	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0000006	OMIM:176670	IEA					I	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0000347	OMIM:176670	IEA					P	HPO:iea[2009-02-17]
OMIM:176670	Hutchinson-Gilford progeria syndrome		HP:0002797	PMID:16838330	PCS					P	HPO:iea[2015-03-22]
OMIM:225290	ECTRODACTYLY-POLYDACTYLY		HP:0001162	OMIM:225290	IEA					P	HPO:iea[2009-02-17]
OMIM:225290	ECTRODACTYLY-POLYDACTYLY		HP:0001839	OMIM:225290	IEA					P	HPO:iea[2009-02-17]
OMIM:225290	ECTRODACTYLY-POLYDACTYLY		HP:0000007	OMIM:225290	IEA					I	HPO:iea[2009-02-17]
OMIM:225290	ECTRODACTYLY-POLYDACTYLY		HP:0001171	OMIM:225290	IEA					P	HPO:iea[2009-02-17]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0003236	PMID:27376152	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0003621	PMID:27376152	PCS		3/3			C	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0002155	PMID:27376152	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0002870	PMID:27376152	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0025383	PMID:27376152	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0002240	PMID:27376152	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0003074	PMID:27376152	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0000819	PMID:27376152	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0000822	PMID:27376152	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0009125	PMID:27376152	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0000956	PMID:27376152	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0001997	PMID:27376152	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0000006	PMID:27376152	PCS					I	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:620679	Lipodystrophy, familial partial, type 8		HP:0002149	PMID:27376152	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-05-09]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0001176	OMIM:221790	PCS					P	HPO:probinson[2012-03-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0100678	OMIM:221790	PCS					P	HPO:probinson[2012-03-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0001939	OMIM:221790	IEA					P	HPO:iea[2009-02-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0000448	OMIM:221790	IEA					P	HPO:iea[2009-02-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0000007	OMIM:221790	IEA					I	HPO:iea[2009-02-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0001833	OMIM:221790	PCS					P	HPO:probinson[2012-03-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0001072	OMIM:221790	PCS					P	HPO:probinson[2012-03-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0000400	OMIM:221790	IEA					P	HPO:iea[2009-02-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0002415	OMIM:221790	PCS					P	HPO:probinson[2012-03-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0001249	OMIM:221790	PCS		20/20			P	HPO:probinson[2012-03-17];HPO:iea[2009-02-17]
OMIM:221790	DERMATOLEUKODYSTROPHY		HP:0005328	OMIM:221790	PCS					P	HPO:probinson[2012-03-17]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000286	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000365	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002540	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001212	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000089	PMID:30827498	PCS		1/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000122	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001250	PMID:30827498	PCS		5/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001252	PMID:30827498	PCS	HP:0003593	8/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002020	PMID:30827498	PCS		5/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001845	PMID:30827498	PCS		4/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002019	PMID:30827498	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000358	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001249	PMID:30827498	PCS		8/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000175	PMID:30827498	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001385	PMID:30827498	PCS		1/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002870	PMID:30827498	PCS		3/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001344	PMID:30827498	PCS		5/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002079	PMID:30827498	PCS		4/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0005301	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001382	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000490	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001263	PMID:30827498	PCS		8/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0003680	PMID:30827498	PCS					C	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0410263	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0010557	PMID:30827498	PCS		3/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0034353	PMID:30827498	PCS		2/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0010880	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002705	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000403	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000568	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000006	PMID:30827498	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000369	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000126	OMIM:618494	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001655	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000341	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0003577	PMID:30827498	PCS		8/8			C	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002521	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000343	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0011833	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001629	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0100704	PMID:30827498	PCS		4/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000414	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001627	OMIM:618494	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000219	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0009765	PMID:30827498	PCS					P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001545	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001320	PMID:30827498	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001562	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002059	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002015	PMID:30827498	PCS		4/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0025352	PMID:30827498	PCS					I	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002650	PMID:30827498	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000194	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0003186	PMID:30827498	PCS		2/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001680	PMID:30827498	PCS		1/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0010654	PMID:30827498	PCS		4/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000348	OMIM:618494	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0001631	PMID:30827498	PCS		2/8			P	HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0000028	PMID:30827498	PCS		1/2			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		HP:0002126	PMID:30827498	PCS		4/8			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-10-06]
OMIM:608687	Spinocerebellar ataxia 20		HP:0002345	PMID:14998916	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0001260	PMID:14998916	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0002066	PMID:14998916	PCS		9/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0003581	PMID:14998916	PCS		14/14			C	HPO:probinson[2012-07-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0002174	PMID:14998916	PCS		2/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0002070	PMID:14998916	PCS		11/14			P	HPO:skoehler[2010-06-20];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0010530	PMID:14998916	PCS		10/14			P	HPO:skoehler[2010-06-18];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0000639	PMID:14998916	PCS		2/14		HP:0012825	P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0001618	PMID:14998916	PCS		10/14			P	HPO:probinson[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0007256	PMID:14998916	PCS		5/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0001620	PMID:14998916	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0000006	PMID:14998916	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0003677	PMID:14998916	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:608687	Spinocerebellar ataxia 20		HP:0007338	PMID:14998916	PCS		10/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-14]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0002069	PMID:23933820	PCS		4/33			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0000750	PMID:23933820	PCS		18/36			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0004322	PMID:20890276	PCS		3/7			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0001761	PMID:20890276	PCS		1/8			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0002376	PMID:23933820	PCS		19/35			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0001250	PMID:20890276	PCS		7/8			P	HPO:iea[2009-02-17];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0002384	PMID:23933820	PCS		4/33			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0010819	PMID:23933820	PCS		1/33			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0001263	PMID:20890276	PCS		4/8			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0003196	PMID:20890276	PCS		1/8			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0001252	PMID:20890276	PCS		4/6			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0002381	PMID:23933820	PCS		9/72			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25];HPO:skoehler[2010-06-20];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0012557	PMID:20890276;PMID:23933820	PCS		21/39			P	HPO:probinson[2021-09-25];HPO:probinson[2014-01-04];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0031491	PMID:23933820	PCS		33/69			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0001518	PMID:20890276	PCS	HP:0003577	1/4			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0011451	PMID:20890276	PCS	HP:0003577	1/3			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0000729	PMID:23933820	PCS		1/36			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0003829	PMID:23933820	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0011098	PMID:23933820	PCS		8/36			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0007334	PMID:23933820	PCS		3/33			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0007018	PMID:23933820	PCS		6/36			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0007359	PMID:20890276	PCS	HP:0003593	1/8			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0007359	PMID:23933820	PCS		14/33			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0007359	PMID:23933820	PCS		4/33			P	HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0000006	PMID:20890276	PCS					I	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25]
OMIM:245570	Epilepsy, focal, with speech disorder and with or without impaired intellectual development		HP:0001249	PMID:20890276;PMID:23933820	PCS		9/44			P	HPO:skoehler[2013-11-28];HPO:probinson[2021-09-25];HPO:probinson[2021-09-25]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000286	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001212	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0004322	PMID:27545675	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001250	PMID:27545675	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001252	PMID:27545675	PCS		6/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001251	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0002020	PMID:27545675	PCS	HP:0003593	2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0003593	PMID:27545675	PCS					C	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0012745	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000718	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0012471	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000316	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0003307	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001763	PMID:27545675	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001249	PMID:27545675	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001344	PMID:27545675	PCS		1/6			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0011968	PMID:27545675	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001382	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001263	PMID:27545675	PCS		6/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0011800	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0100024	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0100023	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000729	PMID:27545675	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000601	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000722	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0007874	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0002307	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000768	PMID:27545675	PCS		1/6			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000322	PMID:27545675	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001276	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001508	PMID:27545675	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000739	PMID:27545675	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0012450	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000733	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000218	PMID:27545675	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0009765	PMID:27545675	PCS		3/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001423	PMID:27545675	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000577	PMID:27545675	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001166	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0002212	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000154	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0002650	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001321	PMID:27545675	PCS		1/5			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0002376	PMID:27545675	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001288	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000430	PMID:27545675	PCS		3/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0005484	PMID:27545675	PCS		2/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0100716	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001631	PMID:27545675	PCS		1/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0007018	PMID:27545675	PCS		2/6			P	HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0000347	PMID:27545675	PCS		1/6			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-10-03]
OMIM:300986	Intellectual developmental disorder, X-linked syndromic, Bain type		HP:0001634	PMID:27545675	PCS		2/6			P	HPO:probinson[2021-10-03]
OMIM:251505	Microphthalmia, isolated, with coloboma 4		HP:0001144	PMID:1621783	PCS		11/196			P	HPO:lccarmody[2018-10-04];HPO:lccarmody[2018-10-04]
OMIM:251505	Microphthalmia, isolated, with coloboma 4		HP:0000482	PMID:1621783	PCS		155/196			P	HPO:lccarmody[2018-10-04]
OMIM:251505	Microphthalmia, isolated, with coloboma 4		HP:0000007	OMIM:251505	IEA					I	HPO:iea[2009-02-17]
OMIM:251505	Microphthalmia, isolated, with coloboma 4		HP:0000568	OMIM:251505	IEA		11/196			P	HPO:iea[2009-02-17];HPO:lccarmody[2018-10-04]
OMIM:251505	Microphthalmia, isolated, with coloboma 4		HP:0000589	OMIM:251505	IEA		185/196			P	HPO:skoehler[2015-12-30];HPO:lccarmody[2018-10-04]
OMIM:222500	DIASTEMATOMYELIA		HP:0000707	OMIM:222500	IEA					P	HPO:iea[2009-02-17]
OMIM:222500	DIASTEMATOMYELIA		HP:0000007	OMIM:222500	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0025441	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0003165	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0005450	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0003072	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0012378	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0031415	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0006051	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0001959	PMID:17710231	PCS		0/1			P	HPO:probinson[2020-08-11];HPO:probinson[2024-03-15]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0000938	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0002905	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0000007	PMID:17710231	PCS					I	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0000103	PMID:17710231	PCS		0/1			P	HPO:probinson[2020-08-11];HPO:probinson[2024-03-15]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0002315	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0002514	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0000787	PMID:17710231	PCS		0/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11];HPO:probinson[2024-03-15]
OMIM:617994	Tumoral calcinosis, hyperphosphatemic, familial, 3		HP:0008208	PMID:17710231	PCS		1/1			P	HPO:probinson[2020-08-11];HPO:probinson[2020-08-11]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000286	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001276	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000044	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000486	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001310	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001250	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0002066	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001252	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0003593	PMID:34730112	PCS		3/3			C	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001290	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001270	PMID:34730112	PCS		2/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000639	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001249	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001347	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001265	PMID:34730112	PCS		2/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0002136	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000054	PMID:34730112	PCS		2/2	MALE		P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001561	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0002650	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001321	PMID:34730112	PCS		2/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0030344	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001263	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0030341	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0002075	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000007	PMID:34730112	PCS					I	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000823	PMID:34730112	PCS		3/3			P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0001511	PMID:34730112	PCS		1/3			P	HPO:probinson[2022-04-03]
OMIM:619761	Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism		HP:0000028	PMID:34730112	PCS		2/2	MALE		P	HPO:probinson[2022-04-03];HPO:probinson[2022-04-03]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0002850	PMID:23129749	PCS					P	HPO:skoehler[2015-07-26];HPO:probinson[2020-08-10]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0410299	PMID:23129749	PCS		2/2			P	HPO:probinson[2020-08-10]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0034839	PMID:23129749	PCS		1/1			P	HPO:probinson[2023-07-18]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0002719	PMID:25352053	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-08-10]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0001744	PMID:25352053	PCS		1/1			P	HPO:skoehler[2015-07-26];HPO:probinson[2020-08-10]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0000006	PMID:25352053	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-10]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0002720	PMID:25352053	PCS	HP:0011463	1/1			P	HPO:probinson[2020-08-10]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0005404	PMID:25352053	PCS	HP:0003593	1/1			P	HPO:probinson[2020-08-10];HPO:probinson[2020-08-10]
OMIM:616452	B-cell expansion with NFKB and T-cell anergy		HP:0005404	PMID:23129749	PCS		4/4			P	HPO:probinson[2020-08-10]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0000365	OMIM:610023	TAS				HP:0012825	P	HPO:skoehler[2014-01-28]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0004322	OMIM:610023	TAS					P	HPO:skoehler[2014-01-28]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0001156	OMIM:610023	TAS					P	HPO:skoehler[2014-11-26]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0007906	OMIM:610023	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0001263	OMIM:610023	TAS				HP:0012825	P	HPO:skoehler[2014-01-28]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0000568	OMIM:610023	TAS					P	HPO:skoehler[2014-01-28]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0000612	OMIM:610023	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0000659	OMIM:610023	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0030084	OMIM:610023	TAS					P	HPO:skoehler[2014-09-21]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0001159	OMIM:610023	IEA					P	HPO:skoehler[2018-10-08]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0007700	OMIM:610023	IEA					P	HPO:skoehler[2015-12-30]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0000006	OMIM:610023	TAS					I	HPO:skoehler[2014-01-28]
OMIM:610023	Brachydactyly, coloboma, and anterior segment dysgenesis		HP:0000589	OMIM:610023	IEA					P	HPO:skoehler[2015-12-30]
OMIM:607239	Deafness, autosomal recessive 33		HP:0000365	OMIM:607239	TAS					P	HPO:skoehler[2017-07-13]
OMIM:607239	Deafness, autosomal recessive 33		HP:0000007	OMIM:607239	TAS					I	HPO:skoehler[2017-07-13]
OMIM:620686	Premature ovarian failure 23		HP:0033085	PMID:31000419;PMID:35991565	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620686	Premature ovarian failure 23		HP:0000869	PMID:31000419;PMID:35991565	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620686	Premature ovarian failure 23		HP:0008222	PMID:34392356;PMID:31000419;PMID:35991565	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620686	Premature ovarian failure 23		HP:0011462	PMID:34392356;PMID:31000419;PMID:35991565	PCS		5/5			C	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620686	Premature ovarian failure 23		HP:0008232	PMID:31000419;PMID:35991565	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620686	Premature ovarian failure 23		HP:0000876	PMID:31000419;PMID:35991565	PCS		3/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620686	Premature ovarian failure 23		HP:0000007	PMID:31000419	PCS					I	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:620686	Premature ovarian failure 23		HP:0031103	PMID:31000419;PMID:35991565	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-05-04]
OMIM:619007	Retinitis pigmentosa 90		HP:0001133	PMID:28412069	PCS		3/4			P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0003621	PMID:28412069	PCS		5/7			C	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0007737	PMID:28412069	PCS		2/7			P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0000662	PMID:28412069	PCS		7/7			P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0000486	PMID:28412069	PCS		1/7			P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0025158	PMID:28412069	PCS		1/7			P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0003593	PMID:28412069	IEA		1/7			C	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0011505	PMID:28412069	PCS		1/7			P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0011463	PMID:28412069	PCS		1/7			C	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0000007	PMID:28412069	PCS					I	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0007663	PMID:28412069	PCS					P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0007843	PMID:28412069	PCS		5/7			P	HPO:probinson[2020-12-01]
OMIM:619007	Retinitis pigmentosa 90		HP:0007722	PMID:28412069	PCS					P	HPO:probinson[2020-12-01]
OMIM:615629	Deafness, autosomal dominant 56		HP:0003621	PMID:23936043	PCS					C	HPO:probinson[2022-12-18]
OMIM:615629	Deafness, autosomal dominant 56		HP:0001751	PMID:23936043	PCS		0/11			P	HPO:probinson[2022-12-18]
OMIM:615629	Deafness, autosomal dominant 56		HP:0000407	PMID:23936043	PCS		11/11			P	HPO:probinson[2022-12-18]
OMIM:615629	Deafness, autosomal dominant 56		HP:0011462	PMID:23936043	PCS					C	HPO:probinson[2022-12-18]
OMIM:615629	Deafness, autosomal dominant 56		HP:0000006	PMID:23936043	PCS					I	HPO:skoehler[2014-02-25];HPO:probinson[2022-12-18]
OMIM:191000	Trochlea of the humerus, aplasia of		HP:0000175	OMIM:191000	IEA					P	HPO:iea[2009-02-17]
OMIM:191000	Trochlea of the humerus, aplasia of		HP:0005792	OMIM:191000	IEA					P	HPO:iea[2009-02-17]
OMIM:191000	Trochlea of the humerus, aplasia of		HP:0000006	OMIM:191000	TAS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21]
OMIM:115300	Carotenemia, familial		HP:0430074	PMID:17951468	PCS		1/1			P	HPO:probinson[2024-02-09]
OMIM:115300	Carotenemia, familial		HP:0004905	PMID:17951468	PCS		1/1			P	HPO:probinson[2015-02-01];HPO:probinson[2024-02-09]
OMIM:115300	Carotenemia, familial		HP:0000006	PMID:17951468	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2024-02-09]
OMIM:115300	Carotenemia, familial		HP:0000951	OMIM:115300	IEA					P	HPO:iea[2009-02-17]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001397	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0004322	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0003199	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001290	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0003073	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0011461	PMID:31355908	PCS					C	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0006530	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0008872	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0002910	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0003546	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0007109	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001562	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001166	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0000252	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0002155	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0002650	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001382	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0000490	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001263	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0012735	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0040075	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0002091	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0000007	PMID:31355908	PCS					I	HPO:probinson[2020-12-04];HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0000821	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001935	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0004428	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:619013	Rajab interstitial lung disease with brain calcifications 2		HP:0001433	PMID:31355908	PCS		1/1			P	HPO:probinson[2020-12-04]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0001771	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003236	OMIM:609200	IEA		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-02-15]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003555	PMID:10958653	PCS		1/1			P	HPO:probinson[2024-02-15]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003687	PMID:10958653	PCS		1/1			P	HPO:probinson[2024-02-15]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003552	OMIM:609200	TAS					P	HPO:probinson[2012-04-26]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003693	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0001271	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003581	PMID:10958653	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2024-02-15]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0001284	OMIM:609200	TAS					P	HPO:probinson[2012-04-26]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0100303	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0009063	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0001638	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003715	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003701	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0000006	PMID:10958653	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-02-15]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003677	OMIM:609200	IEA					C	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0002600	OMIM:609200	IEA					P	HPO:iea[2009-02-17]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003326	OMIM:609200	TAS					P	HPO:probinson[2012-04-26]
OMIM:609200	Myopathy, myofibrillar, 3		HP:0003557	PMID:10958653	PCS		1/1			P	HPO:probinson[2024-02-15]
OMIM:609566	Parietal foramina 3		HP:0002697	OMIM:609566	TAS		20/20			P	HPO:iea[2009-02-17];HPO:skoehler[2015-01-21]
OMIM:609566	Parietal foramina 3		HP:0007385	OMIM:609566	IEA					P	HPO:iea[2009-02-17]
OMIM:609566	Parietal foramina 3		HP:0002084	OMIM:609566	IEA					P	HPO:iea[2009-02-17]
OMIM:609566	Parietal foramina 3		HP:0000006	OMIM:609566	IEA					I	HPO:iea[2009-02-17]
OMIM:300979	Xq25 duplication syndrome		HP:0000286	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0000297	OMIM:300979	TAS		16/27			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0002553	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0000098	PMID:26443594	PCS		3/28			P	HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0000750	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0000574	OMIM:300979	TAS		7/17			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0001321	OMIM:300979	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0002079	OMIM:300979	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0004322	OMIM:300979	TAS		6/28			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0001250	PMID:26443594	PCS		10/31			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0001263	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0000272	PMID:26443594	PCS		23/27			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0001290	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0045075	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0012471	PMID:26443594	PCS		15/26			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0000729	PMID:26443594	PCS		4/15			P	HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0000739	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0001417	PMID:26443594	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0000752	OMIM:300979	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300979	Xq25 duplication syndrome		HP:0001249	PMID:26443594	PCS		33/33			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:300979	Xq25 duplication syndrome		HP:0000303	OMIM:300979	TAS		16/26			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:617980	Erythrocytosis 6		HP:0001900	PMID:18818920	PCS		17/17			P	HPO:probinson[2021-03-30]
OMIM:617980	Erythrocytosis 6		HP:0001899	PMID:18818920	PCS		17/17			P	HPO:probinson[2021-03-30];HPO:probinson[2021-03-30]
OMIM:617980	Erythrocytosis 6		HP:0001901	PMID:18818920	PCS		17/17			P	HPO:probinson[2021-03-30];HPO:probinson[2021-03-30]
OMIM:617980	Erythrocytosis 6		HP:0000006	PMID:18818920	PCS					I	HPO:probinson[2021-03-30];HPO:probinson[2021-03-30]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002444	PMID:35045343	PCS		2/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000365	PMID:35045343	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000480	PMID:35045343	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002000	PMID:35045343	PCS		2/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0001252	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002282	PMID:35045343	PCS		2/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0001270	PMID:35045343	PCS		4/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0033725	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0011265	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0009487	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002816	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0008551	PMID:35045343	PCS		2/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000316	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002119	PMID:35045343	PCS		3/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000218	PMID:35045343	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000158	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000256	PMID:35045343	PCS		2/6			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0001249	PMID:35045343	PCS		3/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0001320	PMID:35045343	PCS		4/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002553	PMID:35045343	PCS		2/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002015	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000750	PMID:35045343	PCS		4/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0011802	PMID:35045343	PCS		2/6			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0032327	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0011304	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0012760	PMID:35045343	PCS		3/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000007	PMID:35045343	PCS					I	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0001338	PMID:35045343	PCS		3/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000348	PMID:35045343	PCS		2/4			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0001852	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000960	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000347	PMID:35045343	PCS		5/6			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0002126	PMID:35045343	PCS		3/5			P	HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0000324	PMID:35045343	PCS		1/5			P	HPO:probinson[2022-05-29];HPO:probinson[2022-05-29]
OMIM:619775	Congenital disorder of deglycosylation 2		HP:0001776	PMID:35045343	PCS		1/4			P	HPO:probinson[2022-05-29]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002421	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0000640	OMIM:600224	TAS					P	HPO:probinson[2013-03-30]
OMIM:600224	Spinocerebellar ataxia 5		HP:0000486	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001310	PMID:22914369	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001272	PMID:22914369	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002066	OMIM:600224	IEA					P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001252	PMID:22914369	PCS		1/1			P	HPO:skoehler[2014-11-26]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001251	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0003593	PMID:22914369	PCS		1/1			C	HPO:skoehler[2014-01-28]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002080	PMID:22914369	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0100543	OMIM:600224	TAS					P	HPO:skoehler[2017-07-13]
OMIM:600224	Spinocerebellar ataxia 5		HP:0007286	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0000317	PMID:22914369	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001347	PMID:22914369	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002311	OMIM:600224	IEA					P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002136	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001583	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001321	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001260	PMID:22914369	PCS		1/1			P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002495	OMIM:600224	IEA					P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0001263	PMID:22914369	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002075	PMID:22914369	PCS		1/1			P	HPO:skoehler[2014-01-28]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002493	OMIM:600224	IEA					P	HPO:skoehler[2018-10-08]
OMIM:600224	Spinocerebellar ataxia 5		HP:0002070	OMIM:600224	IEA					P	HPO:iea[2009-02-17]
OMIM:600224	Spinocerebellar ataxia 5		HP:0011448	PMID:22914369	PCS		1/1			P	HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0007772	OMIM:600224	IEA					P	HPO:skoehler[2010-06-18]
OMIM:600224	Spinocerebellar ataxia 5		HP:0000006	PMID:16429157	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-04-15]
OMIM:600224	Spinocerebellar ataxia 5		HP:0003677	PMID:22914369	PCS		1/1			C	HPO:iea[2009-02-17];HPO:probinson[2023-04-15]
OMIM:614251	Parkinson disease 18		HP:0003587	PMID:21907011	PCS					C	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0002322	PMID:21907011	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0100315	PMID:21907011	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0002067	PMID:21907011	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0001300	PMID:21907011	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0003596	PMID:21907011	PCS					C	HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0003584	PMID:21907011	PCS					C	HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0002063	PMID:21907011	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:614251	Parkinson disease 18		HP:0000006	PMID:21907011	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-27]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0002366	PMID:15106121	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0030007	PMID:15106121	PCS					P	HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0002169	OMIM:602433	TAS		HP:0040283			P	HPO:probinson[2009-02-17]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0003621	PMID:15106121	PCS					C	HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0006825	PMID:9497266	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0001288	PMID:15106121	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0002398	PMID:15106121	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0003487	PMID:15106121	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0006827	PMID:15106121	PCS		2/2			P	HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0003693	PMID:15106121	PCS					P	HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0002460	PMID:15106121	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0010546	PMID:15106121	PCS					P	HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0033383	PMID:15106121	PCS					P	HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0011462	PMID:15106121	PCS					C	HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0040078	PMID:15106121	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0007354	PMID:15106121	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0003405	PMID:15106121	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0000006	PMID:15106121	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0003677	PMID:15106121	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0000764	OMIM:602433	IEA					P	HPO:iea[2009-02-17]
OMIM:602433	Amyotrophic lateral sclerosis 4, juvenile		HP:0001347	PMID:15106121	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-02-20]
OMIM:617770	Spinocerebellar ataxia 46		HP:0001310	OMIM:617770	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617770	Spinocerebellar ataxia 46		HP:0001272	PMID:29053796	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0002066	PMID:29053796	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0001260	PMID:29053796	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0003581	PMID:29053796	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0003390	PMID:29053796	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0002070	PMID:29053796	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0000639	OMIM:617770	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617770	Spinocerebellar ataxia 46		HP:0000514	PMID:29053796	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0008003	PMID:29053796	PCS					P	HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0002403	OMIM:617770	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617770	Spinocerebellar ataxia 46		HP:0003677	PMID:29053796	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-07]
OMIM:617770	Spinocerebellar ataxia 46		HP:0000006	PMID:29053796	PCS					I	HPO:nvasilevsky[2019-03-21];HPO:lccarmody[2019-03-21];HPO:skoehler[2019-03-21];HPO:probinson[2023-02-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001572	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000486	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001773	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002540	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0004322	PMID:30612693	PCS		2/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000160	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001252	PMID:30612693	PCS		9/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0003593	PMID:30612693	PCS					C	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002020	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001251	PMID:30612693	PCS		2/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0040183	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0500041	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000639	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0011463	PMID:30612693	PCS					C	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000316	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000712	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0003307	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002857	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000311	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001249	PMID:30612693	PCS		13/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000252	PMID:30612693	PCS		3/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000574	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002079	PMID:30612693	PCS		4/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002197	PMID:30612693	PCS		4/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000293	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000490	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001263	PMID:30612693	PCS		13/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0008081	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000729	PMID:30612693	PCS		2/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000722	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002944	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0004209	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001257	PMID:30612693	PCS		4/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000322	OMIM:618443	IEA		1/13			P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000369	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000006	PMID:30612693	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000582	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000343	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000463	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001272	PMID:30612693	PCS		3/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002240	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0012448	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0012650	PMID:30612693	PCS		2/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0100704	PMID:30612693	PCS		2/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002317	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000219	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000218	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000411	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002059	PMID:30612693	PCS		3/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002650	PMID:30612693	PCS		4/26			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30];HPO:probinson[2022-09-30];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000276	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0031936	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001321	OMIM:618443	IEA					P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0045025	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0002808	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000426	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000668	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0009237	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000664	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0200055	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001238	PMID:30612693	PCS		1/13			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-09-30]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0001513	OMIM:618443	IEA		HP:0040284			P	HPO:skoehler[2019-09-07]
OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities		HP:0000347	PMID:30612693	PCS		1/13			P	HPO:probinson[2022-09-30]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0003577	PMID:35107634	PCS		1/1			C	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0002188	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0004322	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05];HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0003819	PMID:35107634	PCS		1/1			C	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0001252	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05];HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0003186	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0003282	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0000007	PMID:35107634	PCS					I	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0011344	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05];HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0006466	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0002208	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:619985	Glycosylphosphatidylinositol biosynthesis defect 25		HP:0008070	PMID:35107634	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:614279	46,xy sex reversal 8		HP:0012245	OMIM:614279	TAS					P	HPO:skoehler[2013-04-02]
OMIM:614279	46,xy sex reversal 8		HP:0000062	OMIM:614279	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614279	46,xy sex reversal 8		HP:0000007	OMIM:614279	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614279	46,xy sex reversal 8		HP:0000037	OMIM:614279	TAS					P	HPO:skoehler[2015-01-21]
OMIM:614279	46,xy sex reversal 8		HP:0000028	OMIM:614279	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613270	Corneal dystrophy, fuchs endothelial, 6		HP:0011490	PMID:24094747	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:613270	Corneal dystrophy, fuchs endothelial, 6		HP:0012040	PMID:24094747	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:613270	Corneal dystrophy, fuchs endothelial, 6		HP:0000491	PMID:24094747	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:613270	Corneal dystrophy, fuchs endothelial, 6		HP:0001131	OMIM:613270	IEA					P	HPO:skoehler[2013-01-09]
OMIM:613270	Corneal dystrophy, fuchs endothelial, 6		HP:0007663	PMID:24094747	PCS					P	HPO:lccarmody[2018-10-05];HPO:lccarmody[2018-10-05]
OMIM:613270	Corneal dystrophy, fuchs endothelial, 6		HP:0012038	PMID:24094747	PCS					P	HPO:lccarmody[2018-10-05]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0000286	PMID:30471716	PCS		1/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0002069	PMID:30471716	PCS		7/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0000486	PMID:30471716	PCS		3/5			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0002365	PMID:30471716	PCS		8/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0004322	PMID:30471716	PCS		1/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001250	PMID:30471716	PCS		9/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0002384	PMID:30471716	PCS		3/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001252	PMID:30471716	PCS		7/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0003593	PMID:30471716	PCS		7/9			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0025101	PMID:30471716	PCS		9/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0032794	PMID:30471716	PCS		5/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0012469	PMID:30471716	PCS		2/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0012110	PMID:30471716	PCS		8/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0100307	PMID:30471716	PCS		7/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001629	PMID:30471716	PCS		1/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0011463	PMID:30471716	PCS		1/9			C	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0100704	PMID:30471716	PCS		2/7			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0000316	PMID:30471716	PCS		1/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0025336	PMID:30471716	PCS		5/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001302	PMID:30471716	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001320	PMID:30471716	PCS		7/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0002015	PMID:30471716	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0000252	PMID:30471716	PCS		2/8			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0030303	PMID:30471716	PCS		9/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0003621	PMID:30471716	PCS		1/9			C	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001344	PMID:30471716	PCS		4/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0002079	PMID:30471716	PCS		7/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0031936	PMID:30471716	PCS		8/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0011968	PMID:30471716	PCS		2/7			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001263	PMID:30471716	PCS		9/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0034405	PMID:30471716	PCS		1/9			P	HPO:probinson[2022-12-18]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0005280	PMID:30471716	PCS		1/9			P	HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001339	PMID:30471716	PCS		9/9			P	HPO:skoehler[2019-09-07];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0001257	PMID:30471716	PCS		3/9			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0000006	PMID:30471716	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0004305	PMID:30471716	PCS		HP:0040284			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-11-10]
OMIM:618325	Lissencephaly 9 with complex brainstem malformation		HP:0000369	PMID:30471716	PCS		1/9			P	HPO:probinson[2022-11-10]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0002059	PMID:30120216	PCS		1/2		HP:0003676	P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0003236	PMID:30120216	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0003676	PMID:30120216	PCS					C	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0001344	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0002540	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0002133	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0002188	PMID:30120216	PCS		2/2			P	HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0002376	PMID:30120216	PCS		2/2		HP:0033184	P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0003201	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0001250	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0003593	PMID:30120216	PCS		2/2			C	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0005484	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0011344	PMID:30120216	PCS		2/2			P	HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0100704	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0000007	PMID:30120216	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:618331	Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis		HP:0002445	PMID:30120216	PCS		2/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-30]
OMIM:615615	Immunodeficiency 18		HP:0002850	PMID:15546002	PCS		1/2			P	HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0045080	PMID:15546002	PCS		1/1			P	HPO:probinson[2017-05-29];HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0410242	PMID:15546002	PCS		0/2			P	HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0003460	PMID:15546002	PCS		2/2			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0003593	PMID:15546002	PCS		2/2			C	HPO:skoehler[2014-02-06];HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0031123	OMIM:615615	TAS					P	HPO:probinson[2018-04-13]
OMIM:615615	Immunodeficiency 18		HP:0031379	PMID:15546002;PMID:8490660	PCS		3/3			P	HPO:probinson[2017-05-29];HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0010975	PMID:15546002	PCS		0/2			P	HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0040088	PMID:8490660	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0011463	PMID:8490660	PCS		1/1			C	HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0000007	OMIM:615615	TAS					I	HPO:skoehler[2014-02-06]
OMIM:615615	Immunodeficiency 18		HP:0001888	PMID:15546002	PCS		2/2			P	HPO:skoehler[2014-02-06];HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0000403	PMID:8490660	PCS		1/1			P	HPO:skoehler[2014-02-06]
OMIM:615615	Immunodeficiency 18		HP:0006532	PMID:8490660	PCS		1/1			P	HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0002205	OMIM:615615	TAS					P	HPO:skoehler[2014-02-06]
OMIM:615615	Immunodeficiency 18		HP:0002721	PMID:15546002;PMID:8490660	PCS		3/3			P	HPO:skoehler[2014-06-24];HPO:probinson[2024-03-15];HPO:probinson[2024-03-15]
OMIM:615615	Immunodeficiency 18		HP:0040218	PMID:15546002	PCS		0/2			P	HPO:probinson[2024-03-15]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0002850	PMID:10583958	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0002243	PMID:10583958	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0004432	PMID:10583958	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0003593	PMID:10583958	PCS		1/1			C	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0011109	PMID:10583958	PCS		1/1			P	HPO:skoehler[2013-06-04];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0002718	PMID:10583958	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0000007	PMID:10583958	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0000403	PMID:10583958	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0006532	PMID:10583958	PCS		1/1			P	HPO:skoehler[2012-11-21];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0002843	PMID:10583958	PCS		0/1			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0002720	PMID:10583958	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0001875	PMID:10583958	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-03-26]
OMIM:613502	Agammaglobulinemia 4, autosomal recessive		HP:0004315	PMID:10583958	PCS		1/1			P	HPO:probinson[2022-03-26]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0001276	PMID:8874222	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0002179	OMIM:250800	TAS					P	HPO:skoehler[2009-02-17]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0000252	OMIM:250800	IEA					P	HPO:iea[2009-02-17]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0000486	OMIM:250800	IEA					P	HPO:iea[2009-02-17]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:6000133	PMID:8874222	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0001263	PMID:8874222	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0012119	OMIM:250800	TAS		1/1			P	HPO:probinson[2013-12-15]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0000007	PMID:8874222	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0020045	PMID:8874222	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0001901	OMIM:250800	TAS					P	HPO:iea[2009-02-17]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0000961	PMID:8874222	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2024-01-13]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0002315	OMIM:250800	IEA					P	HPO:probinson[2009-02-17]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0001510	OMIM:250800	IEA					P	HPO:iea[2009-02-17]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0001249	OMIM:250800	IEA					P	HPO:iea[2009-02-17]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0001337	PMID:8874222	PCS		1/1			P	HPO:probinson[2024-01-13]
OMIM:250800	Methemoglobinemia due to deficiency of methemoglobin reductase		HP:0002875	OMIM:250800	TAS					P	HPO:probinson[2013-12-15]
OMIM:207780	AREDYLD		HP:0000968	OMIM:207780	IEA					P	HPO:skoehler[2015-01-14]
OMIM:207780	AREDYLD		HP:0000007	OMIM:207780	TAS					I	HPO:skoehler[2017-07-13]
OMIM:207780	AREDYLD		HP:0004528	OMIM:207780	IEA					P	HPO:iea[2009-02-17]
OMIM:207780	AREDYLD		HP:0000598	OMIM:207780	IEA					P	HPO:iea[2009-02-17]
OMIM:207780	AREDYLD		HP:0000303	OMIM:207780	IEA					P	HPO:iea[2009-02-17]
OMIM:618457	Deafness, autosomal recessive 115		HP:0000407	PMID:30973865	PCS		1/1			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:618457	Deafness, autosomal recessive 115		HP:0000007	PMID:30973865	PCS					I	HPO:skoehler[2019-09-07];HPO:probinson[2023-05-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0012265	PMID:23261302	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0001696	PMID:23261302	PCS		3/6			P	HPO:probinson[2013-03-25];HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0002110	PMID:23261302	PCS		5/6			P	HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0003593	PMID:23261302	PCS		3/6			C	HPO:probinson[2022-03-05]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0033036	PMID:23261302	PCS		6/6			P	HPO:probinson[2022-03-05]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0000007	PMID:23261302	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0000403	PMID:23261302	PCS		6/6			P	HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0002205	PMID:23261302	PCS					P	HPO:probinson[2013-03-25];HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0011108	PMID:23261302	PCS		6/6			P	HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0002643	PMID:23261302	PCS	HP:0003623	3/5			P	HPO:probinson[2020-07-21]
OMIM:608644	Ciliary dyskinesia, primary, 3, with or without situs inversus		HP:0003623	PMID:23261302	PCS		3/6			C	HPO:probinson[2022-03-05]
OMIM:619991	Liver disease, severe congenital		HP:0030215	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003355	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003075	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003593	PMID:35864190	PCS		5/14			C	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0031664	PMID:35864190	PCS		3/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000639	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0004719	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0100806	PMID:35864190	PCS		3/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003348	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003623	PMID:35864190	PCS		7/14			C	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000010	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0012735	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0012465	PMID:35864190	PCS		3/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001738	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0100814	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000007	PMID:35864190	PCS					I	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000403	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0008404	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000520	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000126	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001397	PMID:35864190	PCS		3/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003577	PMID:35864190	PCS		1/14			C	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001399	PMID:35864190	PCS		6/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002243	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002240	PMID:35864190	PCS		10/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0005231	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002480	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0011359	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0033193	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0033196	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0031295	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000737	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000736	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0100827	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0006698	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002910	PMID:35864190	PCS		10/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001942	PMID:35864190	PCS		3/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002014	PMID:35864190	PCS		8/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001682	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003621	PMID:35864190	PCS		1/14			C	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000750	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002013	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0025631	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0004395	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0033994	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002090	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0007010	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0006560	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0009797	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28];HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000348	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001954	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0006568	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000347	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002586	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000286	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0004488	PMID:35864190	PCS	HP:0003577	1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002188	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0010648	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0031508	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001252	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003270	PMID:35864190	PCS		11/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0100327	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001928	PMID:35864190	PCS		7/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001406	PMID:35864190	PCS		5/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001643	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000952	PMID:35864190	PCS		5/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001541	PMID:35864190	PCS		4/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0025053	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0011968	PMID:35864190	PCS		6/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001382	PMID:35864190	PCS		3/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002594	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0003281	PMID:35864190	PCS		5/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0012653	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002904	PMID:35864190	PCS		5/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001537	PMID:35864190	PCS		5/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002902	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000964	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0002901	PMID:35864190	PCS	HP:0003623	1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000047	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000325	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001655	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000023	PMID:35864190	PCS		6/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001629	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001508	PMID:35864190	PCS		10/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001903	PMID:35864190	PCS		5/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000418	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0006254	PMID:35864190	PCS		6/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001987	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001744	PMID:35864190	PCS		10/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001882	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001640	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000034	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0005162	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0012758	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0005280	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0100512	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0100513	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0100598	PMID:35864190	PCS		2/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0000825	PMID:35864190	PCS		5/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0031142	PMID:35864190	PCS		7/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0004905	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001511	PMID:35864190	PCS		9/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001357	PMID:35864190	PCS		1/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001873	PMID:35864190	PCS		3/14			P	HPO:probinson[2022-08-28]
OMIM:619991	Liver disease, severe congenital		HP:0001631	PMID:35864190	PCS	HP:0003577	1/14			P	HPO:probinson[2022-08-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003676	OMIM:252150	TAS					C	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000343	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0001250	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0011935	OMIM:252150	TAS					P	HPO:probinson[2012-06-10]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0011814	OMIM:252150	TAS					P	HPO:probinson[2012-06-11]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003570	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003196	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003808	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000639	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0012471	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003606	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000316	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0008872	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002119	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002932	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000256	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0001249	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003447	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002179	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002059	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003643	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000252	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002510	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0010934	OMIM:252150	TAS					P	HPO:probinson[2012-06-11]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000276	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002079	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000293	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003166	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0001285	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0011942	OMIM:252150	TAS					P	HPO:probinson[2012-06-11]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002171	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0012019	OMIM:252150	IEA					P	HPO:skoehler[2018-10-08]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0011943	OMIM:252150	TAS					P	HPO:probinson[2012-06-11]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0001083	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0034744	OMIM:252150	TAS					P	HPO:probinson[2023-06-05]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0011096	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000804	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0000007	OMIM:252150	IEA					I	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003739	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0002007	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0001510	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003537	OMIM:252150	TAS					P	HPO:skoehler[2014-01-28]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003534	OMIM:252150	IEA					P	HPO:iea[2009-02-17]
OMIM:252150	Molybdenum cofactor deficiency, complementation group A		HP:0003359	OMIM:252150	TAS					P	HPO:probinson[2012-06-10]
OMIM:200170	Acanthosis nigricans with muscle cramps and acral enlargement		HP:0003394	OMIM:200170	IEA					P	HPO:iea[2009-02-17]
OMIM:200170	Acanthosis nigricans with muscle cramps and acral enlargement		HP:0000855	OMIM:200170	IEA					P	HPO:iea[2009-02-17]
OMIM:200170	Acanthosis nigricans with muscle cramps and acral enlargement		HP:0000007	OMIM:200170	IEA					I	HPO:iea[2009-02-17]
OMIM:200170	Acanthosis nigricans with muscle cramps and acral enlargement		HP:0000956	OMIM:200170	IEA					P	HPO:iea[2009-02-17]
OMIM:612783	Immunodeficiency 10		HP:0000100	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0003198	OMIM:612783	IEA					P	HPO:skoehler[2010-06-20]
OMIM:612783	Immunodeficiency 10		HP:0002164	OMIM:612783	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612783	Immunodeficiency 10		HP:0001890	PMID:19420366	PCS		1/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0001252	PMID:19420366	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0002240	PMID:19420366	PCS		2/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0002719	PMID:19420366	PCS		3/3			P	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0100726	PMID:20876309	PCS	HP:0011463	1/1			P	HPO:probinson[2020-01-31]
OMIM:612783	Immunodeficiency 10		HP:0002718	PMID:19420366	PCS		3/3			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0100806	PMID:19420366	PCS		3/3			P	HPO:probinson[2024-03-14];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0001943	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0002716	PMID:19420366	PCS		2/3			P	HPO:skoehler[2010-06-19]
OMIM:612783	Immunodeficiency 10		HP:0006532	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0001744	PMID:19420366	PCS		2/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0003623	PMID:19420366	PCS		2/3			C	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0004315	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0002850	PMID:19420366	PCS		2/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0000010	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0003261	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0040088	PMID:19420366	PCS		0/3			P	HPO:skoehler[2014-11-27];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0000705	PMID:19420366	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0032297	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0000007	PMID:19420366	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0001954	OMIM:612783	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612783	Immunodeficiency 10		HP:0000403	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0000966	OMIM:612783	TAS					P	HPO:skoehler[2017-07-13]
OMIM:612783	Immunodeficiency 10		HP:0007676	PMID:19420366	PCS		3/3			P	HPO:skoehler[2010-06-20];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0001973	PMID:19420366	PCS		3/3			P	HPO:probinson[2024-03-14];HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0002720	PMID:19420366	PCS		1/3			P	HPO:probinson[2024-03-14]
OMIM:612783	Immunodeficiency 10		HP:0002721	PMID:19420366	PCS		3/3			P	HPO:skoehler[2015-01-27];HPO:probinson[2024-03-14]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0002960	PMID:25038750	PCS					P	HPO:skoehler[2015-01-21];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0000164	PMID:25038750	PCS		2/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0002783	PMID:25038750	PCS		1/5			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0004322	PMID:25038750;PMID:25359994	PCS		12/16			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0002242	PMID:25359994	PCS		5/13			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0001890	PMID:25359994	PCS		11/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0003593	PMID:25038750;PMID:25359994	PCS		5/16			C	HPO:probinson[2020-11-26];HPO:probinson[2024-03-15]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0100651	PMID:25038750	PCS	HP:0003623	4/5			P	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0100651	PMID:25359994	PCS		2/13			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0001904	PMID:25359994	PCS		6/13			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0011463	PMID:25038750;PMID:25359994	PCS		7/16			C	HPO:probinson[2020-11-26];HPO:probinson[2024-03-15]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0003623	PMID:25038750	PCS		3/5			C	HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0005942	PMID:25038750	PCS		1/5			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0006515	PMID:25359994	PCS		3/13			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0004313	PMID:25359994	PCS		4/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0001880	PMID:25038750	PCS		0/3			P	HPO:probinson[2020-11-26];HPO:probinson[2024-03-15]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0003621	PMID:25359994	PCS		4/13			C	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0005764	PMID:25359994	PCS		2/13			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0002571	PMID:25359994	PCS		1/13			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0012189	PMID:25359994	PCS		1/13			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0001738	PMID:25038750	PCS		2/5			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0002608	PMID:25038750	PCS		2/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0000964	PMID:25038750	PCS		2/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0000821	PMID:25038750;PMID:25359994	PCS		3/18			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-11-26];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0000823	PMID:25038750	PCS		1/5			P	HPO:skoehler[2014-10-06];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0001973	PMID:25359994	PCS		7/13			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0002788	PMID:25038750	PCS		1/5			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0001433	PMID:25359994	PCS		9/13			P	HPO:probinson[2020-11-26]
OMIM:615952	Autoimmune disease, multisystem, infantile-onset, 1		HP:0000006	PMID:25038750	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-11-26]
OMIM:614494	Retinitis pigmentosa 63		HP:0000662	OMIM:614494	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614494	Retinitis pigmentosa 63		HP:0000543	OMIM:614494	TAS					P	HPO:skoehler[2013-05-31]
OMIM:614494	Retinitis pigmentosa 63		HP:0000510	OMIM:614494	IEA					P	HPO:skoehler[2015-01-19]
OMIM:614494	Retinitis pigmentosa 63		HP:0000622	OMIM:614494	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614494	Retinitis pigmentosa 63		HP:0000006	OMIM:614494	TAS					I	HPO:skoehler[2012-10-17]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0001155	OMIM:221800	IEA					P	HPO:iea[2009-02-17]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0032153	OMIM:221800	IEA					P	HPO:skoehler[2019-02-22]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0001131	OMIM:221800	IEA					P	HPO:iea[2009-02-17]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0008134	OMIM:221800	IEA					P	HPO:iea[2009-02-17]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0000007	OMIM:221800	IEA					I	HPO:iea[2009-02-17]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0007795	OMIM:221800	IEA					P	HPO:iea[2009-02-17]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0200036	OMIM:221800	IEA					P	HPO:skoehler[2010-06-20]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0008039	OMIM:221800	IEA					P	HPO:iea[2009-02-17]
OMIM:221800	Dermochondrocorneal dystrophy		HP:0000212	OMIM:221800	IEA					P	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0001520	OMIM:256450	IEA					P	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0004510	OMIM:256450	IEA					P	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0000825	OMIM:256450	IEA					P	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0002173	OMIM:256450	IEA					P	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0000007	OMIM:256450	IEA					I	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0000006	OMIM:256450	IEA					I	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0001249	OMIM:256450	IEA					P	HPO:iea[2009-02-17]
OMIM:256450	Hyperinsulinemic hypoglycemia, familial, 1		HP:0001325	OMIM:256450	TAS					P	HPO:probinson[2009-02-17]
OMIM:620731	Microphthalmia/coloboma 11		HP:0003577	PMID:33633439;PMID:36695497;PMID:32737437	PCS		28/28			C	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000486	PMID:33633439;PMID:36695497	PCS		2/25			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000541	PMID:36695497	PCS		1/8			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000480	PMID:33633439;PMID:32737437	PCS		8/17			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0011003	PMID:33633439;PMID:32737437	PCS		5/15			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000639	PMID:33633439;PMID:36695497;PMID:32737437	PCS		9/28			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0100019	PMID:32737437	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000613	PMID:33633439	PCS		1/17			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0007750	PMID:33633439	PCS		1/14			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0008499	PMID:33633439	PCS		3/11			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000568	PMID:36695497;PMID:32737437	PCS		2/11			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000612	PMID:33633439;PMID:36695497;PMID:32737437	PCS		16/28			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0007663	PMID:33633439	PCS		6/12			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0007766	PMID:33633439	PCS		7/14			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000567	PMID:36695497;PMID:32737437	PCS		8/11			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000006	PMID:32737437	PCS					I	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:620731	Microphthalmia/coloboma 11		HP:0000588	PMID:36695497;PMID:32737437	PCS		4/11			P	ORCID:0000-0002-0736-9199[2024-06-07]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000286	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001562	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000582	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000750	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000034	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0010775	OMIM:601927	IEA					P	HPO:skoehler[2010-06-18]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0005280	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001629	OMIM:601927	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000506	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0011220	OMIM:601927	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000007	OMIM:601927	IEA					I	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000348	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001789	OMIM:601927	TAS				HP:0012828	P	HPO:probinson[2021-11-24]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001800	OMIM:601927	TAS					P	HPO:probinson[2021-11-24]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000219	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001539	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0004749	OMIM:601927	TAS					P	HPO:skoehler[2012-10-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000455	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001643	OMIM:601927	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0002623	OMIM:601927	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0000311	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001004	OMIM:601927	IEA					P	HPO:iea[2009-02-17]
OMIM:601927	Lymphedema, cardiac septal defects, and characteristic facies		HP:0001631	OMIM:601927	IEA	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0007946	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0000343	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0000486	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0000750	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0009908	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0001328	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0007687	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0000006	OMIM:182875	IEA					I	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0000369	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:182875	Speech development, delayed, with facial asymmetry, strabismus, andtransverse earlobe crease		HP:0000324	OMIM:182875	IEA					P	HPO:iea[2009-02-17]
OMIM:620725	Bethlem myopathy 1B		HP:0001220	PMID:11865138	PCS		5/9			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003687	PMID:11865138	PCS		2/2			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003555	PMID:11865138	PCS		2/2			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003236	PMID:11865138	PCS		9/9			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003581	PMID:11865138	PCS		3/9			C	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003593	PMID:11865138	PCS		1/9			C	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0002460	PMID:11865138	PCS		6/9			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0034677	PMID:11865138;PMID:17886299	PCS		4/11			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0100297	PMID:11865138	PCS		2/2			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0012084	PMID:11865138	PCS		2/2			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0011463	PMID:11865138	PCS		5/9			C	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0034671	PMID:11865138;PMID:17886299	PCS		5/11			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003701	PMID:11865138;PMID:17886299	PCS		11/11			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003713	PMID:11865138	PCS		2/2			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0003306	PMID:17886299	PCS		1/2			P	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0000006	PMID:8782832	PCS					I	HPO:probinson[2024-06-24]
OMIM:620725	Bethlem myopathy 1B		HP:0034391	PMID:17886299	PCS		2/2			P	HPO:probinson[2024-06-24]
OMIM:615946	Myopia 24, autosomal dominant		HP:0003621	PMID:24891338	PCS		5/5			C	HPO:probinson[2022-11-02]
OMIM:615946	Myopia 24, autosomal dominant		HP:0011003	PMID:24891338	PCS		5/5			P	HPO:probinson[2022-11-02]
OMIM:615946	Myopia 24, autosomal dominant		HP:0000006	PMID:24891338	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-02]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0001397	PMID:22226083	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0002155	PMID:22226083	PCS		10/10			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0004322	PMID:22226083	PCS		4/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0002013	PMID:22226083	PCS		3/10			P	HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0001508	PMID:22226083	PCS		1/10			P	HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0001395	PMID:22226083	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0002240	PMID:22226083	PCS		8/8			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0003593	PMID:22226083	PCS		10/10			C	HPO:skoehler[2012-10-17]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0000007	PMID:22226083	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0030948	PMID:22226083	PCS		10/10			P	HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0002910	PMID:22226083	PCS		10/10			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-04-04]
OMIM:614480	Hypertriglyceridemia, transient infantile		HP:0001744	PMID:22226083	PCS		3/7			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-04-04]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001399	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001250	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0003155	PMID:19494034	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0003593	PMID:19494034	PCS		1/1			C	HPO:probinson[2023-05-19]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0002240	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001394	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001251	OMIM:613489	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0012301	PMID:19494034	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0000639	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001508	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0000737	PMID:19494034	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0006892	PMID:19494034	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0002910	PMID:19494034	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001744	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001347	PMID:19494034	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0004798	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0008936	PMID:19494034	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0000252	PMID:19494034	PCS		1/1			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0002059	OMIM:613489	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001344	PMID:19494034	PCS		1/1			P	HPO:skoehler[2014-11-26]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0002079	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0011968	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001263	PMID:19494034	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0100874	PMID:19494034	PCS		1/1			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0002509	PMID:19494034	PCS		1/1			P	HPO:probinson[2023-05-19]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0001999	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0000007	PMID:19494034	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-05-19]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0002205	PMID:19494034	PCS		1/1			P	HPO:skoehler[2012-10-17]
OMIM:613489	Congenital disorder of glycosylation, type IIj		HP:0002028	OMIM:613489	TAS		HP:0040283			P	HPO:skoehler[2013-05-29]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0002015	PMID:9462747;PMID:34225694	PCS	HP:0003584	3/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-04];HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0010628	OMIM:164300	IEA					P	HPO:iea[2009-02-17]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0003676	PMID:34225694	PCS					C	HPO:iea[2009-02-17];HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0003236	PMID:34225694	PCS		0/1			P	HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0003200	PMID:1944407	PCS		0/1			P	HPO:skoehler[2013-05-30];HPO:probinson[2024-03-08]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0001288	PMID:34225694	PCS	HP:0003584	1/1			P	HPO:probinson[2009-02-17];HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0000298	OMIM:164300	TAS					P	HPO:skoehler[2012-10-17]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0007838	PMID:9462747	PCS	HP:0003584	6/6			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0001260	OMIM:164300	IEA					P	HPO:iea[2009-02-17]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0003584	PMID:9462747	PCS		6/6			C	HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0002460	OMIM:164300	IEA					P	HPO:iea[2009-02-17]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0003690	OMIM:164300	IEA					P	HPO:skoehler[2010-06-20]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0000508	PMID:34225694	IEA	HP:0003584	1/1			P	HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0003701	PMID:34225694	PCS	HP:0003584	1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0000006	PMID:9462747	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-04]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0000467	OMIM:164300	IEA					P	HPO:iea[2009-02-17]
OMIM:164300	Oculopharyngeal muscular dystrophy		HP:0001611	PMID:34225694	PCS		1/1			P	HPO:probinson[2022-06-04]
OMIM:129200	Basan syndrome		HP:0001056	PMID:24664640	PCS					P	HPO:skoehler[2010-06-20];HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0001056	PMID:26932190	PCS	HP:0003577	8/8			P	HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0001034	PMID:26932190	PCS		5/8		HP:0025292	P	HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0030044	PMID:26932190	PCS		8/8			P	HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0010621	OMIM:129200	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:129200	Basan syndrome		HP:0025092	OMIM:129200	TAS					P	HPO:skoehler[2017-07-13]
OMIM:129200	Basan syndrome		HP:0031045	PMID:24664640;PMID:26932190	PCS	HP:0003623	11/14			P	HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0032541	PMID:26932190	PCS		7/8			P	HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0001182	OMIM:129200	IEA					P	HPO:iea[2009-02-17]
OMIM:129200	Basan syndrome		HP:0034012	PMID:24664640	PCS	HP:0003581	3/6			P	HPO:probinson[2021-10-03]
OMIM:129200	Basan syndrome		HP:0034012	PMID:26932190	PCS		8/8			P	HPO:probinson[2021-10-03]
OMIM:129200	Basan syndrome		HP:0000968	OMIM:129200	IEA					P	HPO:skoehler[2015-01-14]
OMIM:129200	Basan syndrome		HP:0000954	PMID:26932190	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0007455	PMID:24664640;PMID:26932190	PCS	HP:0003577	15/15			P	HPO:probinson[2021-09-23];HPO:skoehler[2015-01-19];HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0008404	PMID:26932190	PCS		1/8			P	HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0000982	PMID:26932190	PCS		2/8			P	HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0000006	PMID:24664640	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-09-23]
OMIM:129200	Basan syndrome		HP:0003623	PMID:26932190	PCS		8/8			C	HPO:probinson[2021-09-23]
OMIM:619832	Auditory neuropathy, autosomal dominant 3		HP:0000365	PMID:34050020	PCS					P	HPO:probinson[2022-06-27]
OMIM:619832	Auditory neuropathy, autosomal dominant 3		HP:0003584	PMID:34050020	PCS					C	HPO:probinson[2022-06-27]
OMIM:619832	Auditory neuropathy, autosomal dominant 3		HP:0000006	PMID:34050020	PCS					I	HPO:probinson[2022-06-27]
OMIM:619832	Auditory neuropathy, autosomal dominant 3		HP:0001963	PMID:34050020	PCS					P	HPO:probinson[2022-06-27]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0006380	OMIM:300158	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0001288	OMIM:300158	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0001419	OMIM:300158	TAS					I	HPO:skoehler[2012-11-20]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0003680	OMIM:300158	TAS					C	HPO:skoehler[2012-10-14]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0003273	OMIM:300158	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0002804	OMIM:300158	IEA					P	HPO:skoehler[2015-01-19]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0001417	OMIM:300158	TAS					I	HPO:skoehler[2012-10-14]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0006466	OMIM:300158	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300158	Arthrogryposis, congenital, lower limb, X-linked		HP:0001763	OMIM:300158	TAS					P	HPO:skoehler[2012-10-14]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0001265	OMIM:618292	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000286	OMIM:618292	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000494	PMID:28195318	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0001344	PMID:28195318	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000276	PMID:28195318	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0031936	PMID:28195318	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000463	OMIM:618292	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0002066	PMID:28195318	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0001252	PMID:28195318	PCS		2/2			P	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0001263	PMID:28195318	PCS		2/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0003593	PMID:28195318	PCS		2/2			C	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0004482	PMID:28195318	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0001182	OMIM:618292	IEA					P	HPO:skoehler[2019-04-18]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0100807	PMID:28195318	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000689	PMID:28195318	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000007	PMID:28195318	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0002317	PMID:28195318	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000307	PMID:28195318	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000218	PMID:28195318	PCS		1/2			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0001315	PMID:28195318	PCS		1/2			P	HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0000303	PMID:28195318	PCS		1/2			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-09-30]
OMIM:618292	Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia		HP:0003502	OMIM:618292	IEA					P	HPO:skoehler[2019-04-18]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000286	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0002069	PMID:31859446	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001770	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0004322	PMID:31859446;PMID:30903679	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001252	PMID:31859446	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001251	PMID:31859446;PMID:29474920	PCS		1/3			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0003593	PMID:35386260;PMID:29474920	PCS		2/2			C	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0012389	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0045075	PMID:30903679	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0033725	PMID:31859446;PMID:35386260	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0011463	PMID:31859446;PMID:30903679	PCS		2/3			C	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000316	PMID:31859446;PMID:35386260;PMID:30903679	PCS		4/4			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001249	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000677	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001007	PMID:31859446	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0003623	PMID:31859446	PCS		1/2			C	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001265	PMID:31859446	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000252	PMID:31859446;PMID:30903679	PCS		2/3			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0002197	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001382	PMID:31859446	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0002198	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001263	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		5/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001182	PMID:31859446;PMID:29474920	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000448	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000767	PMID:31859446	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0007874	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000047	PMID:31859446;PMID:30903679	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000369	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000006	PMID:29474920	PCS					I	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000341	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000340	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0004220	PMID:30903679	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0100704	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000218	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		4/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0012171	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0009765	PMID:31859446	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0030084	PMID:31859446;PMID:30903679	PCS		3/3			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000653	PMID:30903679	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0008936	PMID:35386260;PMID:30903679	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0002059	PMID:31859446;PMID:35386260	PCS		1/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0002213	PMID:30903679	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0002133	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000431	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0002650	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0031936	PMID:30903679	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0011147	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000508	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		3/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000426	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000307	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		2/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0001511	PMID:31859446;PMID:35386260;PMID:30903679;PMID:29474920	PCS		1/5			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0200055	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0004349	PMID:29474920	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:620719	Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		HP:0000028	PMID:31859446;PMID:30903679	PCS		2/2			P	ORCID:0000-0002-0736-9199[2024-06-09]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000343	PMID:30388402	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000463	PMID:30388402	PCS		2/18			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0001250	PMID:30388402	PCS		0/18			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0001274	PMID:30388402	PCS		3/11			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000581	PMID:30388402	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0001252	PMID:30388402	PCS		11/17			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0001270	PMID:30388402	PCS		11/16			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0012741	PMID:30388402	PCS		2/15			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0045075	PMID:30388402	PCS		4/17			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0033725	PMID:30388402	PCS		2/11			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000718	PMID:30388402	PCS		1/15			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000739	PMID:30388402	PCS		3/15			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000717	PMID:30388402	PCS		4/15			P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0002119	PMID:30388402	PCS		2/11			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000256	PMID:30388402	PCS		13/16			P	HPO:skoehler[2019-09-07];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0001249	PMID:30388402	PCS		18/18			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000494	PMID:30388402	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000750	PMID:30388402	PCS		18/18			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000276	PMID:30388402	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0100710	PMID:30388402	PCS		1/15			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0034054	PMID:30388402	PCS		1/15			P	HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000348	PMID:30388402	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0007018	PMID:30388402	PCS		11/15			P	HPO:probinson[2023-03-03];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000006	PMID:30388402	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-03]
OMIM:618286	Macrocephaly, acquired, with impaired intellectual development		HP:0000446	PMID:30388402	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2023-03-03]
OMIM:619826	Spermatogenic failure 69		HP:0003251	PMID:31985809;PMID:33108537	PCS		3/3			P	HPO:probinson[2022-06-19]
OMIM:619826	Spermatogenic failure 69		HP:0011462	PMID:31985809	PCS		2/2			C	HPO:probinson[2022-06-19]
OMIM:619826	Spermatogenic failure 69		HP:0000007	PMID:31985809	IEA					I	HPO:probinson[2022-06-19]
OMIM:619826	Spermatogenic failure 69		HP:0012205	PMID:31985809;PMID:33108537	PCS		3/3			P	HPO:probinson[2022-06-19]
OMIM:612740	Porphyria, acute hepatic		HP:0003401	OMIM:612740	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612740	Porphyria, acute hepatic		HP:0003577	PMID:2063868	PCS		1/1			C	HPO:probinson[2023-02-11]
OMIM:612740	Porphyria, acute hepatic		HP:0002013	OMIM:612740	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612740	Porphyria, acute hepatic		HP:0001508	PMID:2063868	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-11]
OMIM:612740	Porphyria, acute hepatic		HP:0011848	OMIM:612740	TAS					P	HPO:skoehler[2012-10-17]
OMIM:612740	Porphyria, acute hepatic		HP:0001252	PMID:2063868	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-11]
OMIM:612740	Porphyria, acute hepatic		HP:0003163	PMID:2063868	PCS		1/1			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-02-11]
OMIM:612740	Porphyria, acute hepatic		HP:0001878	OMIM:612740	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612740	Porphyria, acute hepatic		HP:0000007	PMID:2063868	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-11]
OMIM:612740	Porphyria, acute hepatic		HP:0003470	OMIM:612740	IEA					P	HPO:skoehler[2010-06-19]
OMIM:612740	Porphyria, acute hepatic		HP:0002203	PMID:2063868	PCS		1/1			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-02-11]
OMIM:614331	Colorectal cancer, hereditary nonpolyposis, type 6		HP:0006716	PMID:9590282	PCS					P	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:614331	Colorectal cancer, hereditary nonpolyposis, type 6		HP:0000006	PMID:9590282	PCS					I	HPO:probinson[2013-08-10];HPO:probinson[2020-07-20]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0003236	OMIM:612998	TAS					P	HPO:probinson[2012-04-11]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0011463	OMIM:612998	TAS					C	HPO:probinson[2012-04-11]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0005144	OMIM:612998	TAS					P	HPO:probinson[2012-04-11]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0003560	OMIM:612998	IEA					P	HPO:skoehler[2015-07-29]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0007126	OMIM:612998	TAS					P	HPO:probinson[2012-04-11]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0003701	OMIM:612998	TAS					P	HPO:probinson[2012-04-11]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0000006	OMIM:612998	TAS					I	HPO:probinson[2012-04-11]
OMIM:612998	Emery-Dreifuss muscular dystrophy 4, autosomal dominant		HP:0000467	OMIM:612998	TAS					P	HPO:probinson[2012-04-11]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0000486	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0002188	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001332	PMID:36206744	PCS		2/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001250	PMID:36206744	PCS		5/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001252	PMID:36206744	PCS		5/7			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0000020	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0003593	PMID:36206744	PCS		3/8			C	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001251	PMID:36206744	PCS		7/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0010522	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0010543	PMID:36206744	PCS		3/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001270	PMID:36206744	PCS		8/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0000639	PMID:36206744	PCS		4/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0000739	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001302	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0002019	PMID:36206744	PCS		1/8		HP:0012828	P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001249	PMID:36206744	PCS		7/7			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0003623	PMID:36206744	PCS		5/8			C	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0011968	PMID:36206744	PCS		2/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0002076	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001263	PMID:36206744	PCS		8/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0000565	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001257	PMID:36206744	PCS		4/7			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001631	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0000006	PMID:36206744	PCS					I	HPO:probinson[2022-11-24]
OMIM:620094	Neurodevelopmental disorder with eye movement abnormalities and ataxia		HP:0001336	PMID:36206744	PCS		1/8			P	HPO:probinson[2022-11-24]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0002850	PMID:28628108	PCS		3/8			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0001880	PMID:28628108	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0031813	PMID:28628108	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0001047	PMID:28628108	PCS		8/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0003212	PMID:28628108	PCS		5/7			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0002099	PMID:28628108	PCS		5/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0002110	PMID:28628108	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0002090	PMID:28628108	PCS		4/8			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0100279	PMID:28628108	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0032185	PMID:28628108	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0031692	PMID:28628108	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0500093	PMID:28628108	PCS		3/8			P	HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0000006	PMID:28628108	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-12]
OMIM:617638	Immunodeficiency 11B with atopic dermatitis		HP:0002028	PMID:28628108	PCS		1/8			P	HPO:probinson[2023-02-12]
OMIM:619615	Deafness, autosomal recessive 119		HP:0003577	PMID:34626583	PCS		1/3			C	HPO:probinson[2022-01-29]
OMIM:619615	Deafness, autosomal recessive 119		HP:0001250	PMID:34626583	PCS		0/22			P	HPO:probinson[2022-01-29]
OMIM:619615	Deafness, autosomal recessive 119		HP:0000407	PMID:34626583	PCS		22/22			P	HPO:probinson[2022-01-29]
OMIM:619615	Deafness, autosomal recessive 119		HP:0011463	PMID:34626583	PCS		2/3			C	HPO:probinson[2022-01-29]
OMIM:619615	Deafness, autosomal recessive 119		HP:0001263	PMID:34626583	PCS		0/22			P	HPO:probinson[2022-01-29]
OMIM:619615	Deafness, autosomal recessive 119		HP:0000007	PMID:34626583	PCS					I	HPO:probinson[2022-01-29]
OMIM:619615	Deafness, autosomal recessive 119		HP:0001249	PMID:34626583	PCS		0/22			P	HPO:probinson[2022-01-29]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0000750	OMIM:606053	IEA					P	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0002540	OMIM:606053	IEA					P	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0031936	OMIM:606053	IEA					P	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0001382	OMIM:606053	IEA		HP:0040284			P	HPO:skoehler[2019-04-18]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0001263	OMIM:606053	IEA					P	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0003593	OMIM:606053	IEA					C	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0001290	OMIM:606053	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0012760	OMIM:606053	IEA					P	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0000717	OMIM:606053	IEA					P	HPO:iea[2009-02-17]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0000733	OMIM:606053	IEA					P	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0001302	OMIM:606053	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:606053	Intellectual developmental disorder with autism and speech delay		HP:0000006	PMID:30268909	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-07-17]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000343	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000364	PMID:33217309	PCS		0/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0001250	PMID:33217309	PCS		0/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0001290	PMID:33217309	PCS		2/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0001270	PMID:33217309	PCS		3/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0010602	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000639	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0100704	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000316	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0030680	PMID:33217309	PCS		0/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000975	PMID:33217309	PCS		2/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000219	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0009886	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0008936	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000011	PMID:33217309	PCS		2/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0002553	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0002353	PMID:33217309	PCS		2/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0001263	PMID:33217309	PCS		3/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0004370	PMID:33217309	PCS		2/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0002093	PMID:33217309	PCS		3/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0100022	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0011471	PMID:33217309	PCS		3/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000646	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0001137	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000763	PMID:33217309	PCS		2/3			P	HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0000006	PMID:33217309	PCS					I	HPO:probinson[2021-05-06];HPO:probinson[2021-05-06]
OMIM:619173	Neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities		HP:0003557	PMID:33217309	PCS		1/3			P	HPO:probinson[2021-05-06]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0000639	PMID:18327255	PCS		1/1			P	HPO:probinson[2022-12-15]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0000083	PMID:18327255	PCS		1/1			P	HPO:probinson[2022-12-15]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0001263	PMID:18327255	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-15]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0000007	PMID:18327255	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-15]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0010442	PMID:18327255	PCS		0/1			P	HPO:probinson[2022-12-15]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0000510	PMID:18327255	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-15]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0001513	PMID:18327255	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-15]
OMIM:615991	Bardet-Biedl syndrome 14		HP:0001249	PMID:18327255	PCS		1/1			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-12-15]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0000121	OMIM:211900	TAS					P	HPO:probinson[2013-11-24]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0003621	PMID:15599692	PCS		2/2			C	HPO:probinson[2009-02-17];HPO:probinson[2024-03-08]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0003761	PMID:15687324	PCS		3/5			P	HPO:skoehler[2015-01-27];HPO:probinson[2023-03-11]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0001102	OMIM:211900	TAS					P	HPO:probinson[2009-02-17]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0003771	OMIM:211900	TAS					P	HPO:probinson[2009-02-17]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0003155	PMID:15599692	PCS		0/2			P	HPO:probinson[2024-03-08]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0005572	OMIM:211900	TAS					P	HPO:skoehler[2014-06-24]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0031485	OMIM:211900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0005571	OMIM:211900	TAS					P	HPO:probinson[2009-02-17]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0003072	PMID:15599692	PCS		0/2			P	HPO:probinson[2014-05-24];HPO:probinson[2024-03-08]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0031415	PMID:15687324	PCS		5/5			P	HPO:probinson[2023-03-11];HPO:probinson[2023-03-11]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0100774	PMID:15599692	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2024-03-08]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0002905	PMID:15687324;PMID:15599692	PCS		7/7			P	HPO:probinson[2009-02-17];HPO:probinson[2023-03-11];HPO:probinson[2024-03-08]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0006297	OMIM:211900	TAS					P	HPO:probinson[2009-02-17]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0000679	OMIM:211900	TAS					P	HPO:probinson[2009-02-17]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0000843	PMID:15599692	PCS		0/2			P	HPO:probinson[2014-05-24];HPO:probinson[2024-03-08]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0000007	PMID:15687324	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2023-03-11]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0004934	OMIM:211900	TAS					P	HPO:probinson[2009-02-17]
OMIM:211900	Tumoral calcinosis, hyperphosphatemic, familial, 1		HP:0007799	OMIM:211900	TAS					P	HPO:probinson[2009-02-17]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0003577	PMID:22100072	PCS		2/2			C	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0002188	PMID:22100072	PCS		1/2			P	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000023	PMID:22100072	PCS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0002123	PMID:22100072	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0001250	OMIM:614457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0010783	PMID:22100072	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0012444	PMID:22100072	PCS		1/2			P	HPO:skoehler[2013-11-28];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000958	PMID:22100072	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000613	PMID:22100072	PCS		1/2			P	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0002977	OMIM:614457	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0002510	OMIM:614457	TAS		1/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000252	OMIM:614457	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000230	PMID:22100072	PCS		1/2			P	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0002099	OMIM:614457	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0001263	OMIM:614457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0012736	PMID:22100072	PCS		2/2			P	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0011003	PMID:22100072	PCS		1/2			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0034392	PMID:22100072	PCS		2/4			P	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0008064	PMID:22100072	PCS		2/2			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0003819	PMID:22100072	PCS		1/2			C	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000649	OMIM:614457	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0040189	PMID:22100072	PCS		2/2			P	HPO:skoehler[2015-10-05];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0002509	PMID:22100072	PCS		2/2			P	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000007	PMID:22100072	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0007479	PMID:22100072	PCS		1/2			P	HPO:probinson[2023-01-22]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0001510	OMIM:614457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614457	Ichthyosis, spastic quadriplegia, and impaired intellectual development		HP:0000962	OMIM:614457	TAS					P	HPO:skoehler[2012-10-17]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0000110	OMIM:615985	TAS		HP:0040283			P	HPO:skoehler[2014-11-26]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0100259	PMID:14520415	PCS		8/8			P	HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0003577	PMID:14520415	PCS		8/8			C	HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0001696	PMID:14520415	PCS		1/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0001263	PMID:14520415	PCS		8/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0000007	PMID:14520415	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0000510	PMID:14520415	PCS		8/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0000135	PMID:14520415	PCS		5/6			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0000047	PMID:14520415	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0000248	PMID:14520415	PCS		8/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0001249	OMIM:615985	TAS					P	HPO:skoehler[2014-11-26]
OMIM:615985	Bardet-Biedl syndrome 8		HP:0001513	PMID:14520415	PCS		8/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:118750	Choreoathetosis, familial inverted		HP:0001288	OMIM:118750	IEA					P	HPO:iea[2009-02-17]
OMIM:118750	Choreoathetosis, familial inverted		HP:0001250	OMIM:118750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:118750	Choreoathetosis, familial inverted		HP:0000726	OMIM:118750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:118750	Choreoathetosis, familial inverted		HP:0002063	OMIM:118750	IEA					P	HPO:skoehler[2010-06-20]
OMIM:118750	Choreoathetosis, familial inverted		HP:0003593	OMIM:118750	IEA					C	HPO:iea[2009-02-17]
OMIM:118750	Choreoathetosis, familial inverted		HP:0007256	OMIM:118750	IEA					P	HPO:iea[2009-02-17]
OMIM:118750	Choreoathetosis, familial inverted		HP:0007326	OMIM:118750	IEA					P	HPO:iea[2009-02-17]
OMIM:118750	Choreoathetosis, familial inverted		HP:0000006	OMIM:118750	IEA					I	HPO:iea[2009-02-17]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001332	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001250	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0025169	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001252	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001251	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0012708	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0002240	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0003593	PMID:24367056	PCS		1/1			C	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0011951	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0002919	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0011461	PMID:26008905	PCS		1/1			C	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0003648	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0008314	PMID:26008905;PMID:24367056	PCS		2/2			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0003128	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001644	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0002376	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0011968	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001263	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0005484	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0030682	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0005180	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0012043	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0000007	PMID:24367056	PCS					I	HPO:probinson[2021-02-28];HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001712	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0000505	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0000543	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0003811	PMID:26008905	PCS		1/1			C	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001653	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001336	PMID:24367056	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:619167	Mitochondrial complex II deficiency, nuclear type 3		HP:0001655	PMID:26008905	PCS		1/1			P	HPO:probinson[2021-02-28]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0003621	PMID:26257172;PMID:26828946	PCS		3/4			C	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0002378	PMID:26828946	PCS		2/3			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0003376	OMIM:618279	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0001288	OMIM:618279	IEA					P	HPO:skoehler[2019-02-15]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0001761	PMID:26257172;PMID:26828946	PCS		4/4			P	HPO:probinson[2022-10-07];HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0003487	PMID:26828946	PCS		0/3			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0003693	PMID:26257172;PMID:26828946	PCS		4/4			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0003383	PMID:26257172;PMID:26828946	PCS		4/4			P	HPO:probinson[2022-10-07];HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0002460	PMID:26257172	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0012548	PMID:26828946	PCS		3/3			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0011096	PMID:26257172	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0033383	PMID:26257172	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0025708	PMID:26828946	PCS		1/3			C	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0009053	PMID:26828946	PCS		3/3			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0002936	PMID:26257172	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0002359	PMID:26828946	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0006886	PMID:26828946	PCS		3/3			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0003438	PMID:26828946	PCS		2/3			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0000006	PMID:26257172	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0003677	PMID:26828946	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0001765	PMID:26257172	PCS		1/1			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0007328	PMID:26828946	PCS		3/3			P	HPO:probinson[2022-10-07]
OMIM:618279	Charcot-Marie-Tooth disease, demyelinating, type 1G		HP:0006844	PMID:26828946	PCS		2/3			P	HPO:probinson[2022-10-07]
OMIM:610143	Deafness, autosomal recessive 62		HP:0000007	PMID:16650082	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-13]
OMIM:610143	Deafness, autosomal recessive 62		HP:0000399	PMID:16650082	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-13]
OMIM:193005	Vestibulocochlear dysfunction, progressive		HP:0000707	OMIM:193005	IEA					P	HPO:iea[2009-02-17]
OMIM:193005	Vestibulocochlear dysfunction, progressive		HP:0000360	OMIM:193005	IEA					P	HPO:iea[2009-02-17]
OMIM:193005	Vestibulocochlear dysfunction, progressive		HP:0001730	OMIM:193005	IEA					P	HPO:iea[2009-02-17]
OMIM:193005	Vestibulocochlear dysfunction, progressive		HP:0008568	OMIM:193005	IEA					P	HPO:iea[2009-02-17]
OMIM:193005	Vestibulocochlear dysfunction, progressive		HP:0000006	OMIM:193005	IEA					I	HPO:iea[2009-02-17]
OMIM:311900	TARP syndrome		HP:0002245	PMID:20451169	PCS		1/2			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0003577	PMID:20451169	PCS		3/3			C	HPO:probinson[2023-06-09];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0001399	PMID:20451169	PCS		1/2			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0000463	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001250	PMID:20451169	PCS		1/2			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0001252	OMIM:311900	TAS		1/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0000162	OMIM:311900	IEA		1/2			P	HPO:iea[2009-02-17]
OMIM:311900	TARP syndrome		HP:0000085	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001290	OMIM:311900	TAS					P	HPO:skoehler[2017-07-13]
OMIM:311900	TARP syndrome		HP:0012745	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0012725	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0006191	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001508	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0008551	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000316	OMIM:311900	IEA					P	HPO:skoehler[2018-10-08]
OMIM:311900	TARP syndrome		HP:0000239	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000954	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000879	OMIM:311900	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0100309	PMID:20451169	PCS		1/3			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0030084	OMIM:311900	TAS					P	HPO:skoehler[2014-09-21]
OMIM:311900	TARP syndrome		HP:0000218	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000358	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001788	PMID:20451169	PCS		1/2			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0001320	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001562	PMID:20451169	PCS		1/2			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0000175	OMIM:311900	IEA		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0000395	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001762	OMIM:311900	IEA		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0000431	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001321	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000199	OMIM:311900	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001263	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0100259	OMIM:311900	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001838	PMID:20451169	PCS		1/2			P	HPO:probinson[2023-06-09];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0009891	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001419	PMID:20451169	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0000767	OMIM:311900	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:311900	TARP syndrome		HP:0001636	OMIM:311900	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000648	OMIM:311900	TAS		HP:0040283			P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0001511	OMIM:311900	TAS		1/2			P	HPO:skoehler[2014-08-03];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0003811	PMID:20451169	PCS		3/3			C	HPO:probinson[2023-06-09];HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0002305	PMID:20451169	PCS		1/3			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0001631	PMID:20451169	PCS		1/3			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0002984	OMIM:311900	TAS				HP:0012840	P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000369	OMIM:311900	TAS		1/2			P	HPO:skoehler[2014-08-03]
OMIM:311900	TARP syndrome		HP:0000347	PMID:20451169;OMIM:311900	PCS		13/13			P	HPO:probinson[2023-06-09];HPO:iea[2009-02-17]
OMIM:311900	TARP syndrome		HP:0001776	PMID:20451169	PCS		1/3			P	HPO:probinson[2023-06-09]
OMIM:311900	TARP syndrome		HP:0000126	OMIM:311900	TAS					P	HPO:skoehler[2014-08-03]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0002169	PMID:31978608	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0001245	PMID:31978608	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0001761	PMID:26462740	PCS		2/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0001382	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0002110	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0003691	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0033685	PMID:31978608	PCS		1/1			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0012499	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0100550	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0033383	PMID:31978608	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0009053	PMID:31978608	PCS		4/4			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0007141	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0011463	PMID:31978608	PCS		4/4			C	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0009830	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0000978	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0002758	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0001763	PMID:31978608;PMID:26462740	PCS		3/7			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0004933	PMID:26462740	PCS		1/3			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0000006	PMID:26462740	PCS					I	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0001249	PMID:31978608	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:620080	Neuronopathy, distal hereditary motor, type X		HP:0001347	PMID:31978608	PCS		2/4			P	HPO:probinson[2022-12-04]
OMIM:616532	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7		HP:0003621	PMID:26216125	PCS		1/1			C	HPO:probinson[2022-12-19]
OMIM:616532	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7		HP:0001250	PMID:26216125	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-19]
OMIM:616532	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7		HP:0200149	PMID:26216125	PCS		1/1			P	HPO:probinson[2022-12-19]
OMIM:616532	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7		HP:0031179	PMID:26216125	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:616532	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7		HP:0002315	PMID:26216125	PCS		1/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-12-19]
OMIM:616532	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7		HP:0012302	PMID:26216125	PCS		1/2			P	HPO:probinson[2022-12-19]
OMIM:616532	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7		HP:0000006	PMID:26216125	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-12-19]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0006548	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0009938	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000160	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002066	OMIM:606721	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0003196	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000360	PMID:18237401	PCS		1/3			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0100651	PMID:18237401	PCS	HP:0011462	2/3			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000639	PMID:18237401	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000958	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000518	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0011462	PMID:18237401	PCS		1/3			C	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000519	PMID:18237401	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0007485	PMID:18237401	PCS					P	HPO:probinson[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000239	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002936	PMID:18237401	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000956	PMID:18237401	PCS		2/3			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0005328	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0003623	PMID:25898808	PCS		2/2			C	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002155	PMID:18237401	PCS		3/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0003124	PMID:18237401	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0003487	PMID:18237401	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0011968	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002075	PMID:18237401	PCS		2/3			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0040270	OMIM:606721	IEA					P	HPO:skoehler[2019-04-18]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000965	PMID:25898808	PCS		2/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002108	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0003758	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0003635	PMID:11781404	PCS					P	HPO:probinson[2017-09-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000325	PMID:25898808	PCS		2/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000963	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000369	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000006	PMID:18237401	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002202	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0003577	PMID:18237401	PCS		2/3			C	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002169	OMIM:606721	IEA					P	HPO:iea[2009-02-17]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0001278	PMID:18237401	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0005995	PMID:11781404	PCS					P	HPO:probinson[2017-09-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0001310	OMIM:606721	IEA					P	HPO:skoehler[2010-06-20]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000580	PMID:18237401	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0008070	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0100027	PMID:18237401	PCS		2/3			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0001508	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000418	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0007340	PMID:18237401	PCS		2/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0009762	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000855	PMID:18237401	PCS		1/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0009125	PMID:25898808;PMID:18237401	PCS		4/5			P	HPO:probinson[2022-04-01];HPO:iea[2009-02-17];HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0001347	OMIM:606721	IEA					P	HPO:iea[2009-02-17]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002014	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002015	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002013	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0005320	PMID:11781404	PCS					P	HPO:probinson[2017-09-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002092	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0001518	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0002209	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000822	PMID:18237401	PCS	HP:0011462	1/3			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0000103	PMID:25898808	PCS		1/2			P	HPO:probinson[2022-04-01]
OMIM:606721	Lipodystrophy, familial partial, type 7		HP:0001952	OMIM:606721	IEA					P	HPO:iea[2009-02-17]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0000054	OMIM:250790	IEA					P	HPO:skoehler[2018-10-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0003577	PMID:20080843	PCS		1/1			C	HPO:probinson[2023-02-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0000062	PMID:20080843	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0011969	PMID:20080843	PCS		1/1			P	HPO:probinson[2023-02-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0000007	PMID:20080843	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-02-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0012119	PMID:20080843	PCS		1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-02-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0000961	OMIM:250790	IEA					P	HPO:iea[2009-02-17]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0000037	OMIM:250790	TAS					P	HPO:skoehler[2013-05-03]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0000048	PMID:20080843	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0000047	OMIM:250790	IEA					P	HPO:skoehler[2018-10-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0031215	PMID:20080843	PCS		1/1			P	HPO:probinson[2023-02-08]
OMIM:250790	Methemoglobinemia and ambiguous genitalia		HP:0012853	PMID:20080843	PCS		1/1			P	HPO:probinson[2023-02-08]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0000154	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0002883	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0002136	OMIM:614325	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0000486	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0002650	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0002376	OMIM:614325	IEA					P	HPO:skoehler[2018-10-08]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0011968	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0010808	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0001252	OMIM:614325	TAS					P	HPO:skoehler[2014-11-26]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0002020	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0001290	OMIM:614325	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0000007	PMID:19896112	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2020-12-10]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0200134	OMIM:614325	TAS		HP:0040282			P	HPO:skoehler[2013-06-11]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0002307	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0002019	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614325	Pitt-Hopkins-Like syndrome 2		HP:0001642	OMIM:614325	TAS					P	HPO:skoehler[2012-10-17]
OMIM:106220	Aniridia and absent patella		HP:0000518	OMIM:106220	IEA					P	HPO:iea[2009-02-17]
OMIM:106220	Aniridia and absent patella		HP:0006498	OMIM:106220	IEA					P	HPO:iea[2009-02-17]
OMIM:106220	Aniridia and absent patella		HP:0000526	OMIM:106220	IEA					P	HPO:iea[2009-02-17]
OMIM:106220	Aniridia and absent patella		HP:0000006	OMIM:106220	IEA					I	HPO:iea[2009-02-17]
OMIM:106220	Aniridia and absent patella		HP:0000501	OMIM:106220	IEA					P	HPO:iea[2009-02-17]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0001344	PMID:28143899	PCS		1/5			P	HPO:probinson[2022-06-18]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0031936	PMID:28143899	PCS		2/5			P	HPO:probinson[2022-06-18]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0001250	PMID:28143899	PCS		4/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0001263	PMID:28143899	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2022-06-18]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0003593	PMID:28143899	PCS					C	HPO:probinson[2022-06-18]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0000007	PMID:15557513	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-06-18]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0100716	PMID:28143899	PCS		5/5			P	HPO:probinson[2022-06-18]
OMIM:607417	Intellectual developmental disorder, autosomal recessive 2		HP:0007018	PMID:28143899	PCS		2/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-18]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0001562	PMID:28191891	PCS		1/29			P	HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0003577	PMID:28191891	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0003027	PMID:28191891	PCS		2/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0000252	PMID:28191891	PCS		29/29			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0000582	PMID:28191891	PCS		3/29			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0001156	PMID:28191891	PCS		2/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0002750	PMID:28191891	PCS		6/29			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0004322	PMID:28191891	PCS		29/29			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0001263	PMID:28191891	PCS		15/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0003065	PMID:28191891	PCS		2/29			P	HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0010049	PMID:28191891	PCS		3/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0003083	PMID:28191891	PCS		2/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0000007	PMID:28191891	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0006443	PMID:28191891	PCS		2/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0004209	PMID:28191891	PCS		7/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0000878	PMID:28191891	PCS		1/29			P	HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0000444	PMID:28191891	PCS		5/29			P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0001511	PMID:28191891	PCS					P	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0002984	PMID:28191891	PCS		1/29			P	HPO:skoehler[2018-10-08]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0002974	PMID:28191891	PCS		1/29			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-25]
OMIM:617604	Microcephaly, short stature, and limb abnormalities		HP:0009879	PMID:28191891	PCS		1/29			P	HPO:skoehler[2018-10-08]
OMIM:119300	van der Woude syndrome 1		HP:0000175	PMID:20184620	PCS		14/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119300	van der Woude syndrome 1		HP:0003577	PMID:20184620	PCS		24/24			C	HPO:probinson[2022-05-23]
OMIM:119300	van der Woude syndrome 1		HP:0000193	PMID:20184620	PCS		2/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119300	van der Woude syndrome 1		HP:0000196	PMID:19842205;PMID:20184620	PCS		24/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23];HPO:probinson[2022-05-23]
OMIM:119300	van der Woude syndrome 1		HP:0000668	PMID:20184620	PCS		1/24			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119300	van der Woude syndrome 1		HP:0000006	PMID:12219090	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-05-23]
OMIM:119300	van der Woude syndrome 1		HP:0000204	PMID:19842205;PMID:20184620	PCS		22/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-05-23];HPO:probinson[2022-05-23]
OMIM:222448	Donnai-Barrow syndrome		HP:0003577	PMID:25682901	PCS		4/4			C	HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000541	PMID:25682901;PMID:17632512	PCS		2/21			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000365	PMID:25682901	PCS		4/4			P	HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0001250	PMID:17632512	PCS		2/17			P	HPO:iea[2010-04-26];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000260	PMID:12923867;PMID:25682901;PMID:17632512	PCS		27/31			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0005574	PMID:20301732	PCS		100%			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0003196	PMID:12923867	PCS		9/11			P	HPO:iea[2009-02-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0001274	PMID:25682901	PCS		4/4			P	HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000518	PMID:25682901	PCS		1/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0001629	PMID:17632512	PCS		2/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000316	PMID:12923867;PMID:25682901;PMID:17632512	PCS		26/33			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000612	PMID:12923867	PCS		3/6			P	HPO:iea[2009-02-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0000813	PMID:25682901	PCS		HP:0040283			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000879	PMID:17632512	PCS		2/17			P	HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000455	PMID:20301732	PCS		HP:0040281			P	HPO:iea[2010-04-26];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000256	OMIM:222448	TAS					P	HPO:skoehler[2012-10-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0000776	PMID:12923867	PCS		9/13			P	HPO:iea[2009-02-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0000776	PMID:17632512	PCS	HP:0003577	9/17			P	HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000776	PMID:25682901	PCS		1/4			P	HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000358	PMID:12923867	PCS		7/11			P	HPO:iea[2009-02-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0000556	PMID:17632512	PCS		3/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000494	PMID:12923867	PCS		8/11			P	HPO:iea[2009-02-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0001263	PMID:12923867;PMID:25682901;PMID:17632512	PCS		15/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000272	OMIM:222448	TAS					P	HPO:skoehler[2012-10-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0011800	OMIM:222448	TAS					P	HPO:skoehler[2013-11-28]
OMIM:222448	Donnai-Barrow syndrome		HP:0000093	PMID:17632512	PCS		17/17			P	HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0011003	PMID:12923867;PMID:25682901;PMID:17632512	PCS		18/18			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0005280	PMID:20301732	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0100876	PMID:20301732	PCS		HP:0040281			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0007370	PMID:12923867	PCS		11/11			P	HPO:iea[2010-04-26]
OMIM:222448	Donnai-Barrow syndrome		HP:0000529	PMID:20301732	PCS		HP:0040282			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0009110	PMID:20301732	PCS		50%			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000407	PMID:12923867;PMID:17632512	PCS		15/15			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0001537	PMID:17632512	PCS		1/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0000007	PMID:17632512	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0001338	OMIM:222448;PMID:17632512	PCS		15/27			P	HPO:probinson[2022-03-25];HPO:skoehler[2012-10-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0001539	PMID:12923867;PMID:25682901;PMID:17632512	PCS		16/33			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0007676	OMIM:222448	PCS		HP:0040283			P	HPO:iea[2010-04-26]
OMIM:222448	Donnai-Barrow syndrome		HP:0000520	PMID:17632512	PCS		3/17			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-25]
OMIM:222448	Donnai-Barrow syndrome		HP:0002566	PMID:12923867	PCS		3/13			P	HPO:iea[2009-02-17]
OMIM:222448	Donnai-Barrow syndrome		HP:0000369	PMID:12923867	PCS		HP:0040282			P	HPO:iea[2009-02-17]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001331	PMID:25105228	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001177	PMID:33776626;PMID:25105228;PMID:26706854	PCS		0/6			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002389	PMID:25105228	PCS		1/4			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0011819	PMID:25105228	PCS		1/4			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001250	OMIM:603671	TAS					P	HPO:skoehler[2014-10-06]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0004122	PMID:25105228	PCS		4/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002781	OMIM:603671	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0010806	PMID:26706854	PCS		2/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2024-03-28]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001805	OMIM:603671	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000316	PMID:33776626;PMID:25105228;PMID:26706854	PCS		9/9			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-09];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001841	PMID:33776626;PMID:25105228;PMID:26706854	PCS		5/6			P	HPO:probinson[2023-03-09];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0006951	PMID:25105228	PCS		1/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2024-03-28]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001249	OMIM:603671	IEA					P	HPO:skoehler[2010-06-19]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000175	PMID:25105228	PCS		1/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000494	PMID:26706854	PCS		3/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2024-03-28]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002079	PMID:25105228	PCS		1/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0011803	PMID:33776626;PMID:25105228;PMID:26706854	PCS		8/9			P	HPO:skoehler[2012-10-17];HPO:probinson[2024-03-28];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001263	PMID:25105228;PMID:26706854	PCS		6/7			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0005462	PMID:25105228	PCS		3/4			P	HPO:probinson[2023-03-09];HPO:probinson[2024-03-28]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0040075	PMID:25105228	PCS		2/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0010559	PMID:25105228	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09];HPO:probinson[2024-03-28]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002190	PMID:25105228	PCS		2/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000609	PMID:25105228	PCS		1/3			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0034199	PMID:33776626	PCS		1/1			C	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0005736	PMID:25105228	PCS		3/4			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000006	PMID:25105228	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000248	OMIM:603671	IEA					P	HPO:skoehler[2010-06-19]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000204	OMIM:603671	IEA					P	HPO:skoehler[2010-06-19]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000369	PMID:33776626;PMID:25105228;PMID:26706854	PCS		1/9			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0006866	PMID:25105228;PMID:26706854	PCS		6/8			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0003577	PMID:25105228;PMID:26706854	PCS		8/8			C	HPO:probinson[2023-03-09];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:6000295	OMIM:603671	TAS					P	HPO:probinson[2024-02-27]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001274	PMID:33776626;PMID:25105228	PCS		1/5			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-09];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002084	PMID:33776626;OMIM:603671;PMID:25105228;PMID:26706854	PCS		11/19			P	HPO:skoehler[2010-06-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002282	OMIM:603671	IEA					P	HPO:skoehler[2018-10-08]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002119	PMID:25105228	PCS		2/4			P	HPO:skoehler[2010-06-19];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0100629	PMID:25105228;PMID:26706854	PCS		5/5			P	HPO:probinson[2023-03-09];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000455	OMIM:603671	IEA					P	HPO:skoehler[2010-06-19]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000456	OMIM:603671	IEA					P	HPO:skoehler[2019-02-22]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002697	PMID:25105228;PMID:26706854	PCS		4/8			P	HPO:probinson[2023-03-09];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0007968	PMID:25105228	PCS		1/3			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001762	OMIM:603671;PMID:26706854	PCS		12/14			P	HPO:skoehler[2010-06-19];ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000431	PMID:26706854	PCS		4/4			P	HPO:skoehler[2019-02-22];HPO:probinson[2024-03-28]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0002690	PMID:25105228	PCS		3/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0003065	PMID:25105228	PCS		3/3			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0032388	PMID:25105228	PCS		1/4			P	HPO:skoehler[2019-04-18];HPO:probinson[2024-03-28]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0032466	PMID:25105228	PCS		2/2			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:6000787	OMIM:603671	TAS					P	HPO:probinson[2024-08-04]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0012520	PMID:25105228	PCS		1/4			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000506	PMID:25105228	PCS		4/4			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0034014	PMID:25105228	PCS		4/4			P	HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000508	PMID:25105228;PMID:26706854	PCS		5/8			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0025706	PMID:33776626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0001159	OMIM:603671	IEA					P	HPO:skoehler[2010-06-20]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000028	PMID:25105228;PMID:26706854	PCS		2/4			P	ORCID:0000-0002-0736-9199[2024-04-01];HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000501	PMID:25105228	PCS		1/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0004987	PMID:33776626	PCS		1/1			P	ORCID:0000-0002-0736-9199[2024-04-01]
OMIM:603671	Acromelic frontonasal dysostosis		HP:0000545	PMID:25105228	PCS		2/3			P	HPO:skoehler[2014-10-06];HPO:probinson[2023-03-09]
OMIM:601700	Sebaceous gland hyperplasia, familial presenile		HP:0003621	OMIM:601700	TAS					C	HPO:probinson[2022-09-04]
OMIM:601700	Sebaceous gland hyperplasia, familial presenile		HP:0025507	OMIM:601700	TAS					P	HPO:probinson[2022-09-04]
OMIM:601700	Sebaceous gland hyperplasia, familial presenile		HP:0032227	OMIM:601700	TAS					P	HPO:probinson[2022-09-04]
OMIM:601700	Sebaceous gland hyperplasia, familial presenile		HP:0000006	OMIM:601700	IEA					I	HPO:iea[2009-02-17]
OMIM:601700	Sebaceous gland hyperplasia, familial presenile		HP:0000951	OMIM:601700	IEA					P	HPO:iea[2009-02-17]
OMIM:150700	Leiomyoma of vulva and esophagus		HP:0005240	OMIM:150700	IEA					P	HPO:iea[2009-02-17]
OMIM:150700	Leiomyoma of vulva and esophagus		HP:0008665	OMIM:150700	IEA					P	HPO:iea[2009-02-17]
OMIM:150700	Leiomyoma of vulva and esophagus		HP:0000006	OMIM:150700	IEA					I	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0001331	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Microphthalmia, syndromic 7		HP:0003577	PMID:16059943	PCS		11/11			C	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000365	PMID:16059943	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0002023	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0004322	PMID:16059943	PCS		3/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0001250	OMIM:309801	IEA					P	HPO:skoehler[2010-06-18]
OMIM:309801	Microphthalmia, syndromic 7		HP:0011716	PMID:16059943	PCS		1/8			P	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0001274	PMID:16059943	PCS		1/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000580	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000041	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0005152	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0011675	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Microphthalmia, syndromic 7		HP:0010448	PMID:16059943	PCS		1/8			P	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0001629	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000518	PMID:16059943	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Microphthalmia, syndromic 7		HP:0000954	PMID:16059943	PCS		1/8			P	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000612	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000238	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Microphthalmia, syndromic 7		HP:0000659	PMID:16059943	PCS		1/11			P	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0001423	OMIM:309801	IEA					I	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000776	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Microphthalmia, syndromic 7		HP:0001249	PMID:16059943	PCS		2/9			P	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0001545	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000054	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000252	PMID:16059943	PCS		1/8			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Microphthalmia, syndromic 7		HP:0000175	PMID:16059943	PCS		1/8			P	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000013	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0030048	OMIM:309801	TAS					P	HPO:skoehler[2014-09-21]
OMIM:309801	Microphthalmia, syndromic 7		HP:0001263	PMID:16059943	PCS		2/9			P	HPO:probinson[2022-06-25]
OMIM:309801	Microphthalmia, syndromic 7		HP:0011003	PMID:16059943	PCS		1/11			P	HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0012861	OMIM:309801	TAS					P	HPO:skoehler[2014-06-24]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0007398	PMID:16059943	PCS		11/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000568	PMID:16059943	PCS		10/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000647	PMID:16059943	PCS		3/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-06-25]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0008665	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0002623	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0000047	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:309801	Linear skin defects with multiple congenital anomalies 1		HP:0001631	OMIM:309801	IEA					P	HPO:iea[2009-02-17]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0008936	PMID:27616483	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0002059	OMIM:617162	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0002015	PMID:27616483	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0002521	PMID:27616483	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0000252	PMID:27616483	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0001344	OMIM:617162	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0011968	PMID:27616483	PCS		1/2			P	HPO:skoehler[2017-07-13]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0002197	PMID:27616483	PCS		1/2			P	HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0001250	PMID:27616483	PCS		2/2		HP:0031375	P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0001263	PMID:27616483	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0003593	PMID:27616483	PCS		1/2			C	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0001508	PMID:27616483	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0100704	PMID:27616483	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0002509	PMID:27616483	PCS		2/2			P	HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0001558	PMID:27616483	PCS		1/2			P	HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0200134	PMID:27616483	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0002307	PMID:27616483	PCS		1/2			P	HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0001763	PMID:27616483	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0000006	PMID:27616483	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0001337	PMID:27616483	PCS		1/2			P	HPO:probinson[2023-02-26]
OMIM:617162	Epileptic encephalopathy, early infantile, 46		HP:0003623	PMID:27616483	PCS		1/2			C	HPO:probinson[2023-02-26]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0002344	PMID:28604674	PCS					P	HPO:skoehler[2019-02-15];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0003202	PMID:28604674	PCS		2/3			P	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0001310	PMID:28604674	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0001250	PMID:28604674	PCS		1/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0001263	PMID:28604674	PCS		3/3			P	HPO:skoehler[2019-02-15];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0001252	PMID:28604674	PCS		3/3			P	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0003593	PMID:28604674	PCS		3/3			C	HPO:skoehler[2019-02-15];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0002280	PMID:28604674	PCS		1/3			P	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0011923	PMID:28604674	PCS		2/2			P	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0001508	PMID:28604674	PCS		2/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0000639	PMID:28604674	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0003819	PMID:28604674	PCS		2/3			C	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0000407	PMID:28604674	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0009830	PMID:28604674	PCS		1/3			P	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0000007	PMID:28604674	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0008872	PMID:28604674	PCS		2/3			P	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0002119	PMID:28604674	PCS		1/3			P	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0002205	PMID:28604674	PCS		1/3			P	HPO:probinson[2021-05-31]
OMIM:618251	Mitochondrial complex I deficiency, nuclear type 31		HP:0001336	PMID:28604674	PCS		1/3			P	HPO:probinson[2021-05-31]
OMIM:607371	Dystonia, juvenile-onset		HP:0002751	PMID:12325076	PCS	HP:0003621	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0000175	PMID:12325076	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0002015	PMID:12325076	PCS		2/2			P	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0003577	PMID:12325076	PCS		2/2			C	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0000882	PMID:12325076	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0002571	PMID:12325076	PCS	HP:0011463	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0031959	PMID:12325076	PCS	HP:0003621	2/2			P	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0001260	PMID:12325076	PCS	HP:0003621	2/2			P	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0001270	PMID:12325076	PCS		2/2			P	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0010553	PMID:12325076	PCS	HP:0011462	2/2			P	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0000518	PMID:12325076	PCS		1/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0000407	PMID:12325076	PCS	HP:0011463	2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0001518	PMID:12325076	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0011342	PMID:12325076	PCS		2/2			P	HPO:probinson[2012-07-21];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0008796	PMID:12325076	PCS		2/2			P	HPO:probinson[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0007024	PMID:12325076	PCS		2/2			P	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0000348	PMID:12325076	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0002505	PMID:12325076	PCS	HP:0011462	2/2			P	HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0007325	PMID:12325076	PCS	HP:0011462	2/2			P	HPO:probinson[2012-07-21];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0000006	PMID:16685646	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:607371	Dystonia, juvenile-onset		HP:0000204	PMID:12325076	PCS		2/2			P	HPO:iea[2009-02-17];HPO:probinson[2022-09-05]
OMIM:616268	Arboleda-Tham syndrome		HP:0011939	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000483	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000486	PMID:25728775	PCS		4/8			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001332	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0002780	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0002020	PMID:25728775	PCS		3/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0002141	PMID:32041641	PCS		5/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001290	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0010051	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000358	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0002553	PMID:32041641	PCS		5/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000010	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000252	PMID:32041641	PCS		5/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001344	PMID:25728775;PMID:32041641	PCS		7/9			P	HPO:probinson[2022-06-24];HPO:skoehler[2018-10-08];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000490	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0011800	PMID:32041641	PCS		3/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0006185	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0006342	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000767	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000646	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000403	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0100818	PMID:32041641	PCS		5/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000648	PMID:25728775	PCS		1/2			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001852	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000520	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0007678	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000369	PMID:32041641	PCS		4/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000006	PMID:32041641	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000126	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000341	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0003577	PMID:25728775	PCS		4/4			C	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001156	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0012724	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0100785	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0008593	PMID:32041641	PCS		3/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0100704	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0000733	PMID:32041641	PCS		4/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000219	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0006610	PMID:32041641	PCS		5/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001544	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000455	PMID:32041641	PCS		4/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000456	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0002015	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001684	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0002098	PMID:32041641	PCS	HP:0003623	1/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0003186	PMID:32041641	PCS		1/4			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000509	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000508	PMID:25728775	PCS		2/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0100559	PMID:32041641	PCS		1/4			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001319	OMIM:616268	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616268	Arboleda-Tham syndrome		HP:0002007	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000465	PMID:32041641	PCS		0/5			P	HPO:probinson[2020-08-02];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0002643	OMIM:616268	TAS					P	HPO:skoehler[2015-12-30]
OMIM:616268	Arboleda-Tham syndrome		HP:0000286	PMID:25728775;PMID:32041641	PCS		5/9			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0002100	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001250	PMID:32041641	PCS		3/5			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000160	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001252	PMID:25728775	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0045074	PMID:32041641	PCS		3/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0020045	PMID:32041641	PCS		4/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0002857	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0025336	PMID:25728775	PCS		4/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001643	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0001642	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001763	PMID:32041641	PCS		4/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001249	PMID:32041641	PCS		5/5			P	HPO:skoehler[2015-07-29];HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001765	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000175	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0011968	PMID:25728775	PCS		3/4			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001263	PMID:25728775;PMID:32041641	PCS		7/9			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0011451	PMID:25728775	PCS		4/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000729	PMID:25728775;PMID:32041641	PCS		4/8			P	HPO:probinson[2020-08-02];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0025325	PMID:32041641	PCS		5/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001538	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000565	PMID:25728775	PCS		2/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000322	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0008689	PMID:25728775	PCS		1/2			P	HPO:probinson[2022-06-24];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000325	PMID:32041641	PCS		4/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000324	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000385	PMID:32041641	PCS		3/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0002562	PMID:32041641	PCS		3/4			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0010109	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0040080	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001629	PMID:25728775	PCS		1/3			P	HPO:skoehler[2015-05-31];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0009765	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0006895	PMID:32041641	PCS		3/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0002714	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0000774	PMID:32041641	PCS		5/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0009129	PMID:32041641	PCS		4/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000154	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0008936	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000395	PMID:32041641	PCS		5/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001363	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0000276	PMID:32041641	PCS		4/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0002970	PMID:32041641	PCS		1/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0031936	PMID:25728775	PCS		4/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001480	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0011272	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000308	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0007210	PMID:32041641	PCS		4/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000426	PMID:25728775;PMID:32041641	PCS		4/13			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000307	PMID:32041641	PCS		3/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0002205	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001357	OMIM:616268	TAS					P	HPO:skoehler[2015-05-31]
OMIM:616268	Arboleda-Tham syndrome		HP:0001511	PMID:32041641	PCS	HP:0030674	2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0001511	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000389	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001510	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0001631	PMID:25728775;PMID:32041641	PCS		4/8			P	HPO:skoehler[2015-05-31];HPO:probinson[2020-08-02];HPO:probinson[2022-06-24];HPO:probinson[2022-06-24]
OMIM:616268	Arboleda-Tham syndrome		HP:0000545	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0000303	PMID:32041641	PCS		2/5			P	HPO:probinson[2020-08-02]
OMIM:616268	Arboleda-Tham syndrome		HP:0002566	PMID:25728775	PCS		1/4			P	HPO:probinson[2022-06-24]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001342	OMIM:263400	IEA					P	HPO:iea[2009-02-17]
OMIM:263400	Erythrocytosis, familial, 2		HP:0002641	OMIM:263400	IEA					P	HPO:iea[2009-02-17]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001297	OMIM:263400	IEA					P	HPO:iea[2009-02-17]
OMIM:263400	Erythrocytosis, familial, 2		HP:0003621	PMID:12844285	PCS		1/7			C	HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0003593	PMID:23403324	PCS		1/1			C	HPO:probinson[2022-03-11];HPO:probinson[2022-12-03]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001050	OMIM:263400	IEA					P	HPO:iea[2009-02-17]
OMIM:263400	Erythrocytosis, familial, 2		HP:0033644	PMID:12844285;PMID:23403324	PCS		7/9			P	HPO:probinson[2022-03-11];HPO:probinson[2022-12-03];HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0002092	PMID:23403324	PCS		1/1			P	HPO:probinson[2022-03-11];HPO:probinson[2022-12-03]
OMIM:263400	Erythrocytosis, familial, 2		HP:0012378	OMIM:263400	TAS					P	HPO:skoehler[2013-10-22]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001508	PMID:23403324	PCS	HP:0011463	1/1			P	HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0011463	PMID:12844285;PMID:23403324	PCS		7/8			C	HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0002619	OMIM:263400	IEA					P	HPO:iea[2009-02-17]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001900	PMID:12844285;PMID:23403324	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-11];HPO:probinson[2022-03-11];HPO:probinson[2022-12-03];HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0000007	PMID:12844285	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001899	PMID:12844285	PCS		7/7			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0002615	OMIM:263400	IEA					P	HPO:iea[2009-02-17]
OMIM:263400	Erythrocytosis, familial, 2		HP:0002315	PMID:23403324	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-11]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001898	OMIM:263400	IEA					P	HPO:iea[2009-02-17]
OMIM:263400	Erythrocytosis, familial, 2		HP:0001028	OMIM:263400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:618245	Mitochondrial complex I deficiency, nuclear type 24		HP:0003676	PMID:22200994	PCS					C	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618245	Mitochondrial complex I deficiency, nuclear type 24		HP:0002151	PMID:22200994	PCS		1/1			P	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618245	Mitochondrial complex I deficiency, nuclear type 24		HP:0001252	PMID:22200994	PCS		1/1			P	HPO:probinson[2022-12-15]
OMIM:618245	Mitochondrial complex I deficiency, nuclear type 24		HP:0003593	PMID:22200994	PCS		1/1			C	HPO:skoehler[2019-02-15];HPO:probinson[2022-12-15]
OMIM:618245	Mitochondrial complex I deficiency, nuclear type 24		HP:0000007	PMID:22200994	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-15]
OMIM:618245	Mitochondrial complex I deficiency, nuclear type 24		HP:0011923	PMID:22200994	PCS		2/2			P	HPO:probinson[2022-12-15]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0000594	OMIM:613310	TAS		HP:0040283			P	HPO:skoehler[2014-04-13]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0007917	OMIM:613310	TAS		HP:0040283			P	HPO:skoehler[2014-04-13]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0001493	PMID:20159111	PCS		2/6			P	HPO:probinson[2022-10-10]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0007663	PMID:20159111	PCS		3/6			P	HPO:skoehler[2015-07-26];HPO:probinson[2022-10-10]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0000505	PMID:20159111	PCS		3/6			P	HPO:skoehler[2014-04-13];HPO:probinson[2022-10-10]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0030490	PMID:20159111	PCS					P	HPO:skoehler[2015-07-29];HPO:probinson[2022-10-10]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0001147	OMIM:613310	IEA					P	HPO:skoehler[2018-10-08]
OMIM:613310	Exudative vitreoretinopathy 5		HP:0000006	PMID:20159111	PCS					I	HPO:skoehler[2014-04-13];HPO:probinson[2022-10-10]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000483	PMID:25138099	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000582	PMID:24680889	PCS		5/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000343	PMID:25138099	PCS		2/2			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000486	PMID:25480035	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000463	PMID:25138099;PMID:25480035	PCS		4/9			P	HPO:probinson[2020-12-12];HPO:skoehler[2017-07-13];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0003593	PMID:25138099	PCS		2/2			C	HPO:probinson[2022-06-03]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000319	PMID:24680889	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000414	PMID:25138099	PCS		2/2			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000678	PMID:25480035	PCS		3/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0003307	PMID:25480035	PCS		2/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000219	PMID:24680889	PCS		5/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0002714	PMID:25138099	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0001249	PMID:24680889	PCS		7/7			P	HPO:skoehler[2015-01-19];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000494	PMID:24680889;PMID:25138099	PCS		2/9			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000750	PMID:24680889;PMID:25138099	PCS		8/9			P	HPO:probinson[2020-12-12];HPO:skoehler[2014-11-26];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0002650	PMID:24680889	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000431	PMID:25138099	PCS		2/2			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0031936	PMID:25138099	PCS		2/2			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0011968	PMID:24680889	PCS		5/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0001263	PMID:25480035	PCS		7/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000294	PMID:25138099	PCS		2/2			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0005280	PMID:24680889	PCS		3/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0100259	PMID:24680889	PCS		1/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0002808	PMID:24680889	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000729	PMID:24680889	PCS		5/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0100559	PMID:24680889	PCS		2/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000508	PMID:24680889	PCS		1/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000348	PMID:24680889	PCS		1/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000722	PMID:25480035	PCS		3/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0002307	PMID:25480035	PCS		3/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0001852	PMID:25138099	PCS		1/2			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000664	PMID:24680889	PCS		5/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000047	PMID:25480035	PCS					P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000960	PMID:24680889	PCS		2/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000006	PMID:24680889	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000248	PMID:24680889	PCS		3/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0009836	PMID:25138099	PCS		1/2			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000369	PMID:24680889	PCS		5/7			P	HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000347	PMID:24680889	PCS		3/7			P	HPO:skoehler[2014-08-24];HPO:probinson[2020-12-12]
OMIM:615761	Intellectual developmental disorder, autosomal dominant 23		HP:0000545	PMID:25138099	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2020-12-12]
OMIM:605572	Abdominal obesity-metabolic syndrome quantitative trait locus 2		HP:0000822	OMIM:605572	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605572	Abdominal obesity-metabolic syndrome quantitative trait locus 2		HP:0012743	OMIM:605572	TAS					P	HPO:skoehler[2017-07-13]
OMIM:605572	Abdominal obesity-metabolic syndrome quantitative trait locus 2		HP:0000006	OMIM:605572	TAS					I	HPO:skoehler[2017-07-13]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0002135	PMID:23255827	PCS		10/12			P	HPO:skoehler[2013-01-09];HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0003621	PMID:23255827	PCS		1/6			C	HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0001300	PMID:23255827	PCS		1/13			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0003596	PMID:23255827	PCS		1/6			C	HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0002076	PMID:23255827	PCS		3/13			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0003584	PMID:23255827	PCS		1/6			C	HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0000716	OMIM:615007	TAS					P	HPO:skoehler[2015-12-30]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0000726	PMID:23255827	PCS		1/13			P	HPO:skoehler[2013-01-21];HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0011462	PMID:23255827	PCS		3/6			C	HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0007302	PMID:23255827	PCS		1/13			P	HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0007018	PMID:23255827	PCS		1/13			P	HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0000006	PMID:23255827	PCS					I	HPO:skoehler[2013-01-11];HPO:probinson[2022-12-15]
OMIM:615007	Basal ganglia calcification, idiopathic, 4		HP:0000666	PMID:23255827	PCS		1/13			P	HPO:probinson[2022-12-15]
OMIM:617610	Polycystic kidney disease 5		HP:0003774	PMID:28530676	PCS	HP:0011462	4/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0003621	PMID:28530676	PCS		2/7			C	HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0005565	PMID:28530676	PCS		3/7			P	HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0011463	PMID:28530676	PCS		4/7			C	HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0004719	PMID:28530676	PCS		7/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0003593	PMID:28530676	PCS		1/7			C	HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0000822	PMID:28530676	PCS		5/7			P	HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0000007	PMID:28530676	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0001433	PMID:28530676	PCS		1/7			P	HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0000113	PMID:28530676	PCS		6/7			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0000105	PMID:28530676	PCS		2/7			P	HPO:probinson[2022-12-14]
OMIM:617610	Polycystic kidney disease 5		HP:0003677	PMID:28530676	PCS					C	HPO:skoehler[2018-10-08];HPO:probinson[2022-12-14]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0030799	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0001880	PMID:28747427;PMID:30309848	PCS		2/2			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0001363	PMID:28747427	PCS		1/1		HP:0012828	P	HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0002650	PMID:28747427	PCS		1/1			P	HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0003212	PMID:30309848	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0003212	PMID:28747427	PCS		1/1			P	HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0000491	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0002110	PMID:28747427	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0003040	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0012758	PMID:30309848	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0009473	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0002827	PMID:30309848	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0500093	PMID:30309848	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0000007	PMID:30309848	PCS					I	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0000403	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0001217	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0000678	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0000964	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0000964	PMID:28747427	PCS	HP:0011463	1/1			P	HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0002944	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0000158	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0002205	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0002205	PMID:28747427	PCS	HP:0003593	1/1			P	HPO:probinson[2020-05-15]
OMIM:618523	Hyper-IgE recurrent infection syndrome 4, autosomal recessive		HP:0002028	PMID:30309848	PCS		1/1			P	HPO:probinson[2020-05-15];HPO:probinson[2020-05-15]
OMIM:601072	Deafness, autosomal recessive 8/10		HP:0003577	PMID:11137999	PCS					C	HPO:probinson[2021-02-28]
OMIM:601072	Deafness, autosomal recessive 8/10		HP:0000407	PMID:11137999	PCS					P	HPO:skoehler[2010-06-18];HPO:probinson[2021-02-28]
OMIM:601072	Deafness, autosomal recessive 8/10		HP:0011463	PMID:11137999	PCS					C	HPO:probinson[2012-07-19];HPO:probinson[2021-02-28]
OMIM:601072	Deafness, autosomal recessive 8/10		HP:0000007	PMID:11137999	PCS					I	HPO:probinson[2009-02-17];HPO:probinson[2021-02-28]
OMIM:300831	CK syndrome		HP:0000286	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000582	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000486	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0001250	OMIM:300831	TAS	HP:0003593				P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0001290	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000737	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000718	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000678	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0003307	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000218	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000752	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0001302	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000278	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0001249	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000358	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0003103	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000275	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000252	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000750	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0002650	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000276	OMIM:300831	TAS					P	HPO:skoehler[2012-10-15]
OMIM:300831	CK syndrome		HP:0001382	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0001263	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000272	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0002808	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0001419	PMID:19377476	PCS					I	HPO:skoehler[2012-10-14];HPO:probinson[2023-03-25]
OMIM:300831	CK syndrome		HP:0011297	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000426	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0007874	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0001533	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0000347	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:300831	CK syndrome		HP:0002126	OMIM:300831	TAS					P	HPO:skoehler[2012-10-14]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0001320	PMID:24989451	PCS		4/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0003202	PMID:24989451	PCS		8/11		HP:0012828	P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0000365	PMID:24989451	PCS		9/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0002079	PMID:24989451	PCS		4/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0002120	PMID:24989451	PCS		3/8			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0011968	PMID:24989451	PCS		6/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0001263	PMID:24989451	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0001285	PMID:24989451	PCS		8/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0003593	PMID:24989451	PCS		11/11			C	HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0002093	PMID:24989451	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0002280	PMID:24989451	PCS		2/8			P	HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0034392	PMID:24989451	PCS		3/11			P	HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0001508	PMID:24989451	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0003819	PMID:24989451	PCS					C	HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0000737	PMID:24989451	PCS		4/11			P	HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0000007	PMID:24989451	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0002878	PMID:24989451	PCS		11/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0000505	PMID:24989451	PCS		9/11			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0001308	PMID:24989451	PCS		1/11			P	HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0007269	PMID:24989451	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0001324	PMID:24989451	PCS		6/11		HP:0012828	P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-30]
OMIM:616081	Pontocerebellar hypoplasia, type 1C		HP:0001347	PMID:24989451	PCS		1/11			P	HPO:probinson[2022-10-30]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0003621	PMID:33512449	PCS		3/6			C	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0003453	PMID:33512449	PCS		2/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0001890	PMID:33512449	PCS		4/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0003593	PMID:33512449	PCS		2/6			C	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0002240	PMID:33512449	PCS		5/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0100651	PMID:33512449	PCS		1/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0010976	PMID:33512449	PCS		2/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0011107	PMID:33512449	PCS		1/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0011974	PMID:33512449	PCS		1/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0025708	PMID:33512449	PCS		1/6			C	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0009098	PMID:33512449	PCS		1/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0012156	PMID:33512449	PCS		1/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0012234	PMID:33512449	PCS		2/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0002719	PMID:33512449	PCS					P	HPO:probinson[2022-06-08];HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0000403	PMID:33512449	PCS		2/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0002716	PMID:33512449	PCS		2/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0001417	PMID:33512449	PCS					I	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0020102	PMID:33512449	PCS		1/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0005528	PMID:33512449	PCS		3/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0001510	PMID:33512449	PCS		1/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0001873	PMID:33512449	PCS		5/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0001744	PMID:33512449	PCS		5/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0001875	PMID:33512449	PCS		6/6			P	HPO:probinson[2022-06-08]
OMIM:301078	Immunodeficiency 98 with autoinflammation, X-linked		HP:0004315	PMID:33512449	PCS		5/6			P	HPO:probinson[2022-06-08]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000252	PMID:18241066	PCS		4/5			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000494	PMID:18241066	PCS		1/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000431	PMID:18241066	PCS		1/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000276	PMID:18241066	PCS		1/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000581	PMID:18241066	PCS		1/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0003196	PMID:18241066	PCS		2/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0002162	PMID:18241066	PCS		1/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0001263	OMIM:611936	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0012745	OMIM:611936	TAS					P	HPO:skoehler[2014-03-24]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0001090	OMIM:611936	TAS					P	HPO:skoehler[2012-10-17]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000414	PMID:18241066	PCS		3/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0006114	PMID:18241066	PCS		2/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000311	PMID:18241066	PCS		3/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000256	PMID:18241066	PCS		1/5			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0001763	PMID:18241066	PCS		2/4			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0000006	OMIM:611936	IEA					I	HPO:iea[2010-09-13]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0001513	PMID:18241066	PCS		3/5			P	HPO:iea[2010-09-14]
OMIM:611936	Chromosome 3q29 duplication syndrome		HP:0001249	PMID:18241066	PCS		3/4			P	HPO:iea[2010-09-14]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0000252	OMIM:304100	IEA					P	HPO:iea[2009-02-17]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0000486	PMID:16650080	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001321	OMIM:304100	TAS					P	HPO:probinson[2012-06-10]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0002079	PMID:16650080	PCS		2/2			P	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001250	OMIM:304100	IEA					P	HPO:iea[2009-02-17]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001263	PMID:16650080	PCS		2/2			P	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0002251	PMID:16650080	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0003083	PMID:16650080	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0032327	OMIM:304100	IEA					P	HPO:skoehler[2019-04-18]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0034198	PMID:16650080	PCS		2/2			C	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001419	PMID:16650080	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0007068	OMIM:304100	TAS					P	HPO:probinson[2012-06-10]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0000238	OMIM:304100	IEA					P	HPO:iea[2009-02-17]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001338	PMID:16650080	PCS		1/2			P	HPO:iea[2009-02-17]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0002119	PMID:16650080	PCS		2/2			P	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0000218	PMID:16650080	PCS		1/2			P	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001763	PMID:16650080	PCS		2/2			P	HPO:probinson[2023-05-19]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001257	OMIM:304100	IEA					P	HPO:iea[2009-02-17]
OMIM:304100	Corpus callosum, partial agenesis of, X-linked		HP:0001249	PMID:16650080	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2023-05-19]
OMIM:133700	Exostoses, multiple, type I		HP:0002762	PMID:11432960;PMID:34012378;PMID:35106951	PCS		38/38			P	HPO:probinson[2022-03-31];HPO:probinson[2022-03-31];HPO:probinson[2022-03-31]
OMIM:133700	Exostoses, multiple, type I		HP:0003621	PMID:34012378	PCS		2/2			C	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:133700	Exostoses, multiple, type I		HP:0003068	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0004322	PMID:11432960	PCS		1/27			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:133700	Exostoses, multiple, type I		HP:0003276	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0010049	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0000918	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0011463	PMID:35106951	PCS		8/8			C	HPO:probinson[2022-03-31]
OMIM:133700	Exostoses, multiple, type I		HP:0002812	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0003406	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0002318	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0002857	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0006765	PMID:11432960;PMID:34012378;PMID:35106951	PCS		7/37			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-31];HPO:probinson[2022-03-31]
OMIM:133700	Exostoses, multiple, type I		HP:0000006	PMID:7550340	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-31]
OMIM:133700	Exostoses, multiple, type I		HP:0003105	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:133700	Exostoses, multiple, type I		HP:0000896	OMIM:133700	IEA					P	HPO:iea[2009-02-17]
OMIM:612581	Intellectual developmental disorder, autosomal dominant 4		HP:0000331	OMIM:612581	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612581	Intellectual developmental disorder, autosomal dominant 4		HP:0011800	OMIM:612581	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612581	Intellectual developmental disorder, autosomal dominant 4		HP:0001159	OMIM:612581	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612581	Intellectual developmental disorder, autosomal dominant 4		HP:0000006	PMID:19012874	TAS					I	HPO:probinson[2013-04-06]
OMIM:612581	Intellectual developmental disorder, autosomal dominant 4		HP:0001249	PMID:19012874	TAS					P	HPO:probinson[2013-04-06]
OMIM:612581	Intellectual developmental disorder, autosomal dominant 4		HP:0001831	OMIM:612581	IEA					P	HPO:skoehler[2018-10-08]
OMIM:612581	Intellectual developmental disorder, autosomal dominant 4		HP:0000577	OMIM:612581	IEA					P	HPO:skoehler[2019-04-18]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0002850	PMID:8462096	PCS					P	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0005403	PMID:8462096	PCS					P	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0005479	PMID:8462096	PCS					P	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0004432	PMID:8462096	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0004430	PMID:8462096	PCS					P	HPO:skoehler[2009-02-17];HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0002240	OMIM:300400	IEA					P	HPO:iea[2009-02-17]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0003593	PMID:8462096	IEA		2/3			C	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0002090	OMIM:300400	IEA					P	HPO:iea[2009-02-17]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0012177	PMID:8462096	PCS					P	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0009098	PMID:8462096	PCS		1/3			P	HPO:probinson[2013-12-15];HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0001508	PMID:8462096	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0001419	PMID:8462096	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0007274	OMIM:300400	IEA					P	HPO:iea[2009-02-17]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0000778	OMIM:300400	TAS					P	HPO:probinson[2013-12-15]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0000988	OMIM:300400	IEA					P	HPO:skoehler[2010-06-20]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0006532	PMID:8462096	PCS		1/3			P	HPO:probinson[2020-11-27];HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0002841	OMIM:300400	IEA					P	HPO:iea[2009-02-17]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0002720	PMID:8462096	PCS					P	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0003347	PMID:8462096	PCS					P	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0002028	OMIM:300400	IEA					P	HPO:iea[2009-02-17]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0003623	PMID:8462096	PCS		1/3			C	HPO:probinson[2020-11-27]
OMIM:300400	Severe combined immunodeficiency, X-linked		HP:0004315	PMID:8462096	PCS					P	HPO:probinson[2020-11-27]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0003431	PMID:32367058	PCS		11/42			P	HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0002650	PMID:32367058	PCS					P	HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0008959	PMID:32367058	IEA		26/44			P	HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0009053	PMID:32367058	PCS		43/44			P	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0001288	PMID:32367058	PCS					P	HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0001761	PMID:32367058	PCS					P	HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0002495	PMID:32367058	PCS		17/40			P	HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0007078	PMID:32367058	PCS		26/40			P	HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0000007	PMID:32367058	PCS					I	HPO:probinson[2020-08-12];HPO:probinson[2020-08-12]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0033124	PMID:32367058	PCS		10/10			P	HPO:probinson[2020-10-13]
OMIM:618912	Sorbitol dehydrogenase deficiency with peripheral neuropathy		HP:0007328	PMID:32367058	PCS		13/39			P	HPO:probinson[2020-08-12]
OMIM:607832	Focal segmental glomerulosclerosis 3, susceptibility to		HP:0000083	PMID:17713465	PCS					P	HPO:probinson[2013-03-04]
OMIM:607832	Focal segmental glomerulosclerosis 3, susceptibility to		HP:0000097	PMID:17713465	PCS					P	HPO:probinson[2013-03-04]
OMIM:607832	Focal segmental glomerulosclerosis 3, susceptibility to		HP:0000790	PMID:17713465	PCS					P	HPO:probinson[2013-03-04]
OMIM:607832	Focal segmental glomerulosclerosis 3, susceptibility to		HP:0000822	PMID:17713465	PCS					P	HPO:probinson[2013-03-04]
OMIM:607832	Focal segmental glomerulosclerosis 3, susceptibility to		HP:0000093	PMID:17713465	PCS					P	HPO:probinson[2013-03-04]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0001760	OMIM:137200	TAS					P	HPO:skoehler[2012-11-16]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0003202	OMIM:137200	IEA					P	HPO:skoehler[2015-01-21]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0003236	PMID:22961002	PCS		12/14			P	HPO:skoehler[2012-11-16];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0002411	PMID:22961002	PCS		2/50			P	HPO:iea[2009-02-17];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0003676	PMID:22961002	PCS					C	HPO:skoehler[2012-11-16];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0003621	PMID:22961002	PCS		44/50			C	HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0003552	PMID:22961002	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0003394	PMID:22961002	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0002380	OMIM:137200	TAS					P	HPO:skoehler[2012-11-16]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0003390	PMID:22961002	PCS					P	HPO:skoehler[2012-11-16];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0034351	PMID:22961002	PCS		44/46			P	HPO:probinson[2022-09-05]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0011463	PMID:22961002	PCS		4/50			C	HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0011462	PMID:22961002	PCS		2/50			C	HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0009027	OMIM:137200	TAS					P	HPO:skoehler[2012-11-16]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0000007	PMID:22961002	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0002936	PMID:22961002	PCS		23/28			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-08-22]
OMIM:137200	Neuromyotonia and axonal neuropathy, autosomal recessive		HP:0000975	OMIM:137200	IEA					P	HPO:iea[2009-02-17]
OMIM:204100	Leber congenital amaurosis, type II		HP:0001320	OMIM:204100	IEA					P	HPO:iea[2009-02-17]
OMIM:204100	Leber congenital amaurosis, type II		HP:0001099	PMID:12960219	PCS		1/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000563	PMID:16505055	PCS		0/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000662	PMID:12960219;PMID:16505055	PCS		14/14			P	HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0001483	OMIM:204100	IEA					P	HPO:iea[2009-02-17]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000580	OMIM:204100	IEA					P	HPO:iea[2009-02-17]
OMIM:204100	Leber congenital amaurosis, type II		HP:0003593	PMID:12960219;PMID:16505055	PCS		14/14			C	HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0030825	PMID:12960219	PCS		6/13			P	HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000518	PMID:12960219	PCS		0/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000639	PMID:16505055	PCS		1/1			P	HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000618	OMIM:204100	IEA					P	HPO:iea[2009-02-17]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000613	PMID:12960219;PMID:16505055	PCS		0/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10];HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000007	PMID:12960219	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0007663	PMID:12960219;PMID:16505055	PCS		14/14			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10];HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0000543	PMID:12960219	PCS		9/13			P	HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0007688	PMID:12960219	PCS		13/13			P	HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0007843	PMID:12960219;PMID:16505055	PCS		13/13			P	HPO:probinson[2022-03-10]
OMIM:204100	Leber congenital amaurosis, type II		HP:0001249	PMID:12960219	PCS		2/13			P	HPO:iea[2009-02-17];HPO:probinson[2022-03-10]
OMIM:620241	Hydrocephalus, congenital, 5, susceptibility to		HP:0002410	PMID:29983323	PCS					P	HPO:probinson[2023-06-12]
OMIM:620241	Hydrocephalus, congenital, 5, susceptibility to		HP:0003577	PMID:29983323	PCS					C	HPO:probinson[2023-06-12]
OMIM:620241	Hydrocephalus, congenital, 5, susceptibility to		HP:0003829	PMID:29983323	PCS					I	HPO:probinson[2023-06-12]
OMIM:620241	Hydrocephalus, congenital, 5, susceptibility to		HP:0000006	PMID:29983323	PCS					I	HPO:probinson[2023-06-12]
OMIM:620241	Hydrocephalus, congenital, 5, susceptibility to		HP:0010953	PMID:29983323	PCS					P	HPO:probinson[2023-06-12]
OMIM:610382	Prosopagnosia, hereditary		HP:0010528	OMIM:610382	IEA					P	HPO:skoehler[2015-01-27]
OMIM:610382	Prosopagnosia, hereditary		HP:0000006	OMIM:610382	TAS					I	HPO:skoehler[2012-10-17]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0000252	PMID:31616000	PCS		3/18			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0001363	PMID:31616000	PCS	HP:0003577	3/14			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0000750	PMID:31616000	PCS	HP:0011463	18/20			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0002650	PMID:31616000	PCS					P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0002376	PMID:31616000	PCS		2/11			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0002497	PMID:31616000	PCS		5/13			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0001250	PMID:31616000	PCS		11/20			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0001382	PMID:31616000	PCS		3/9			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0001290	PMID:31616000	PCS		5/13			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0001270	PMID:31616000	PCS	HP:0011463	13/19			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0000729	PMID:31616000	PCS		15/20			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0000739	PMID:31616000	PCS		4/12			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0012450	PMID:31616000	PCS		9/15			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0000733	PMID:31616000	PCS		13/19			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0007018	PMID:31616000	PCS		4/14			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0000006	PMID:31616000	PCS					I	HPO:probinson[2020-08-13];HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0001249	PMID:31616000	PCS		19/20			P	HPO:probinson[2020-08-13]
OMIM:618906	Intellectual developmental disorder with autistic features and language delay, with or without seizures		HP:0000687	PMID:31616000	PCS					P	HPO:probinson[2020-08-13]
OMIM:249000	Meckel syndrome 1		HP:0002023	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0100490	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001252	PMID:27377014;PMID:33193692	PCS		2/2			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001408	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000319	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0000316	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000238	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0002419	PMID:27377014;PMID:33193692	PCS		2/2			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0009466	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0002617	OMIM:249000	IEA					P	HPO:skoehler[2018-10-08]
OMIM:249000	Meckel syndrome 1		HP:0000835	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0006872	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0004639	OMIM:249000	TAS					P	HPO:probinson[2013-04-14]
OMIM:249000	Meckel syndrome 1		HP:0025336	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001643	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000113	PMID:17377820	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:249000	Meckel syndrome 1		HP:0001600	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000175	PMID:35360848	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0000252	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001341	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001583	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001344	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0000695	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0002198	PMID:35360848	PCS		3/3			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0005343	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000130	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001263	PMID:27377014;PMID:33193692	PCS		2/2			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0003241	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0100259	PMID:35360848	PCS		3/3			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0034198	PMID:27377014;PMID:35360848	PCS		4/4			C	HPO:probinson[2022-07-11];HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0002308	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000800	PMID:35360848	PCS		0/3			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0000007	PMID:17377820	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-14]
OMIM:249000	Meckel syndrome 1		HP:0000601	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000568	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0009931	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0006267	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001539	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000204	PMID:35360848	PCS		0/3			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0000369	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001671	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0002323	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000340	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0002089	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001195	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000061	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001274	PMID:27377014;PMID:35360848	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-07-11];HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0002085	PMID:35360848;PMID:17377820	PCS		9/9			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14];HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0000180	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001829	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001746	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000337	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001305	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000612	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000219	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0002119	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001747	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0030084	OMIM:249000	TAS					P	HPO:skoehler[2014-09-21]
OMIM:249000	Meckel syndrome 1		HP:0000537	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001623	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001744	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000033	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0008936	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001562	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000154	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001883	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001321	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0031936	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001162	PMID:17377820;PMID:33193692	PCS		4/6			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-14];HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0001680	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000470	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000508	PMID:27377014	PCS		1/1			P	HPO:probinson[2022-07-11]
OMIM:249000	Meckel syndrome 1		HP:0006563	PMID:17377820	PCS		1/1			P	HPO:probinson[2021-02-14]
OMIM:249000	Meckel syndrome 1		HP:0006487	OMIM:249000	IEA					P	HPO:skoehler[2010-06-18]
OMIM:249000	Meckel syndrome 1		HP:0001511	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0001830	PMID:17377820	PCS		5/5			P	HPO:probinson[2021-02-14];HPO:probinson[2021-02-14]
OMIM:249000	Meckel syndrome 1		HP:0001159	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000069	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000465	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000028	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0002566	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000347	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:249000	Meckel syndrome 1		HP:0000104	OMIM:249000	IEA					P	HPO:iea[2009-02-17]
OMIM:200400	Achalasia, familial esophageal		HP:0002571	OMIM:200400	IEA					P	HPO:iea[2009-02-17]
OMIM:200400	Achalasia, familial esophageal		HP:0001370	OMIM:200400	IEA					P	HPO:iea[2009-02-17]
OMIM:200400	Achalasia, familial esophageal		HP:0001097	OMIM:200400	IEA					P	HPO:iea[2009-02-17]
OMIM:200400	Achalasia, familial esophageal		HP:0000217	OMIM:200400	IEA					P	HPO:iea[2009-02-17]
OMIM:200400	Achalasia, familial esophageal		HP:0000007	OMIM:200400	IEA					I	HPO:iea[2009-02-17]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0003621	PMID:25390740	PCS		1/9			C	HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0001993	PMID:25390740	PCS		9/9		HP:0012828	P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0002919	PMID:25390740	PCS		6/9			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0011968	PMID:25390740	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0011463	PMID:25390740	PCS		7/9			C	HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0001263	PMID:25390740	PCS					P	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0003593	PMID:25390740	PCS		1/9			C	HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0012734	PMID:25390740	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0000007	PMID:25390740	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0000006	PMID:25390740	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-10-01]
OMIM:616095	Monocarboxylate transporter 1 deficiency		HP:0001249	PMID:25390740	PCS		3/9			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-10-01]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0003577	PMID:17336976	PCS		1/1			C	HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000343	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000260	PMID:17336976	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0001250	OMIM:614872	TAS					P	HPO:probinson[2013-02-24]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0006829	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0002240	OMIM:614872	TAS					P	HPO:probinson[2013-02-24]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0012368	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000639	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000518	PMID:17336976	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000218	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0001522	PMID:17336976	PCS		4/4			C	HPO:probinson[2013-02-24];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000358	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000952	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0005469	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0008935	OMIM:614872	TAS					P	HPO:probinson[2013-02-24]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0001762	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0011968	OMIM:614872	TAS					P	HPO:probinson[2013-02-24]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0004491	PMID:17336976	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0010655	OMIM:614872	TAS					P	HPO:probinson[2013-02-24]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0034298	PMID:17336976	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0034297	PMID:17336976	PCS		1/1			P	HPO:probinson[2022-09-05]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000348	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000007	PMID:12851857	PCS					I	HPO:probinson[2013-01-09];HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0002126	PMID:17336976	PCS		1/1			P	HPO:probinson[2022-06-22]
OMIM:614872	Peroxisome biogenesis disorder 7A (zellweger)		HP:0000369	PMID:17336976	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-06-22]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0002025	PMID:21507892	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0003577	PMID:21507892	PCS		10/10			C	HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0001263	PMID:21507892	PCS		1/10			P	HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:6000101	OMIM:248450	TAS					P	HPO:probinson[2024-01-06]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000528	PMID:21507892	PCS		1/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0009553	PMID:21507892	PCS		7/9			P	HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000316	PMID:21507892	PCS		4/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000007	PMID:21507892	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000568	OMIM:248450	PCS				HP:0012828	P	HPO:iea[2012-04-01]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000579	OMIM:248450	IEA					P	HPO:iea[2009-02-17]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0001539	PMID:21507892	PCS		3/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000625	PMID:21507892	PCS		4/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0001126	PMID:21507892	PCS		1/10			P	HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000455	PMID:21507892	PCS		3/10			P	HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0001545	PMID:21507892	PCS		2/10			P	HPO:iea[2009-02-17];HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000456	PMID:21507892	PCS		9/10			P	HPO:probinson[2023-06-11]
OMIM:248450	Manitoba oculotrichoanal syndrome		HP:0000148	PMID:21507892	PCS		1/7			P	HPO:probinson[2023-06-11]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002069	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001773	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001250	PMID:28166369	PCS		10/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0003196	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002020	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001290	PMID:28166369	PCS		8/8			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0012469	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000319	PMID:23863341;PMID:28166369	PCS		4/11			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0010055	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000678	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0007687	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000311	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000278	PMID:26358754;PMID:23863341	PCS		2/2			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000358	PMID:28166369	PCS		3/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001007	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0006315	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002553	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000252	PMID:26358754;PMID:23863341	PCS		2/2			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001385	PMID:23863341;PMID:28166369	PCS		2/11			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000494	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000175	PMID:28166369	PCS		2/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002353	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001344	PMID:26358754;PMID:28166369	PCS		11/11			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000453	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002079	PMID:26358754;PMID:28166369	PCS		2/11			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000490	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001263	PMID:23863341;PMID:28166369	PCS		11/11			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000294	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0011800	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001182	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0010711	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0012385	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000729	PMID:28166369	PCS		2/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0031165	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002507	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000601	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0007359	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000322	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000325	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000324	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000687	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001276	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000341	PMID:28166369	PCS		2/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000582	PMID:23863341;PMID:28166369	PCS		2/11			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002521	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0003577	PMID:26358754	PCS		1/1			C	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000463	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000460	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0033349	PMID:28166369	PCS		7/10			C	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001629	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000817	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000733	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000219	PMID:28166369	PCS		2/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0030084	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002714	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001423	PMID:23863341	PCS					I	HPO:probinson[2021-01-24];HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000776	PMID:23863341	PCS	HP:0003577	1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0008936	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000396	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000750	PMID:23863341	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0002650	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001883	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0031936	PMID:23863341	PCS	HP:0003593	1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001285	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0010773	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0011344	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0009471	PMID:28166369	PCS		1/10			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001511	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0000664	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0200055	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001510	PMID:26358754	PCS		1/1			P	HPO:probinson[2021-01-24]
OMIM:301044	Developmental and epileptic encephalopathy 85, with or without midline brain defects		HP:0001631	PMID:28166369	PCS		3/10			P	HPO:probinson[2021-01-24]
OMIM:600807	Asthma, susceptibility to		HP:0002099	OMIM:600807	IEA					P	HPO:iea[2009-02-17]
OMIM:600807	Asthma, susceptibility to		HP:0001426	OMIM:600807	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:600807	Asthma, susceptibility to		HP:0000006	OMIM:600807	TAS					I	HPO:nvasilevsky[2019-03-07]
OMIM:600807	Asthma, susceptibility to		HP:4000007	OMIM:600807	TAS					P	HPO:probinson[2021-10-03]
OMIM:600807	Asthma, susceptibility to		HP:0032933	OMIM:600807	TAS					P	HPO:probinson[2022-04-15]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002069	PMID:30032983	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002540	PMID:30032983	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001310	PMID:30032983	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002123	PMID:30032983	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001272	PMID:30032983	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002066	PMID:30032983	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002063	PMID:30032983	PCS		2/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001252	PMID:30032983	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0010862	PMID:30032983	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0011463	PMID:30032983	PCS		3/3			C	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0000752	PMID:30032983	PCS		2/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001320	PMID:30032983	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001344	PMID:30032983	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0000750	PMID:30032983	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001288	PMID:30032983	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002079	PMID:30032983	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002376	PMID:30032983	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001263	PMID:30032983	PCS		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002194	PMID:30032983	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0012434	PMID:30032983	PCS		3/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0031358	PMID:30032983	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0032792	PMID:30032983	PCS		1/3			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0000007	PMID:30032983	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0002307	PMID:30032983	PCS		1/2			P	HPO:probinson[2023-03-05]
OMIM:618090	Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum		HP:0001337	PMID:30032983	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-03-05]
OMIM:609823	Deafness, autosomal recessive 28		HP:0003593	OMIM:609823	IEA					C	HPO:iea[2009-02-17]
OMIM:609823	Deafness, autosomal recessive 28		HP:0000007	OMIM:609823	IEA					I	HPO:iea[2009-02-17]
OMIM:609823	Deafness, autosomal recessive 28		HP:0008625	OMIM:609823	TAS					P	HPO:skoehler[2009-02-17]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0002188	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0004322	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0030674	PMID:35325049	PCS		1/2			C	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0001272	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0000162	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0003593	PMID:35325049	PCS		1/2			C	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0010585	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0012368	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0033725	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0008434	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0002415	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0000278	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0004976	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0008936	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0003026	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0002059	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0000175	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0001344	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0002650	PMID:35325049	PCS		2/2			P	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0002673	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0002079	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0004233	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0011968	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0001382	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0002451	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0003042	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0001263	PMID:35325049	PCS		2/2			P	HPO:probinson[2023-06-12];HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0001181	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0000007	PMID:35325049	PCS					I	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0004626	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0000201	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:620269	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia		HP:0000666	PMID:35325049	PCS		1/2			P	HPO:probinson[2023-06-12]
OMIM:305550	Fingerprint body myopathy		HP:0003198	OMIM:305550	IEA					P	HPO:skoehler[2010-06-20]
OMIM:305550	Fingerprint body myopathy		HP:0001939	OMIM:305550	IEA					P	HPO:iea[2009-02-17]
OMIM:305550	Fingerprint body myopathy		HP:0001417	OMIM:305550	IEA					I	HPO:iea[2009-02-17]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0000321	OMIM:300428	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0004322	OMIM:300428	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0007010	OMIM:300428	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0000053	OMIM:300428	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0004482	OMIM:300428	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0000218	OMIM:300428	TAS					P	HPO:skoehler[2017-07-13]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0001417	OMIM:300428	TAS					I	HPO:skoehler[2017-07-13]
OMIM:300428	Intellectual developmental disorder, X-linked 2		HP:0001249	PMID:6839531	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2025-09-26]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001265	PMID:26996948	PCS					P	HPO:probinson[2017-06-24]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0002059	PMID:26996948	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001344	PMID:26996948	PCS		1/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0000750	PMID:26996948	PCS					P	HPO:probinson[2017-06-24]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001321	PMID:26996948	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0002079	PMID:26996948	PCS		1/5			P	HPO:probinson[2017-06-24];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001250	PMID:26996948	PCS		3/5			P	HPO:probinson[2017-06-24];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0003155	PMID:26996948	PCS		0/5			P	HPO:probinson[2017-06-24];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001263	PMID:26996948	PCS		5/5			P	HPO:probinson[2017-06-24];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0006829	PMID:26996948	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001251	PMID:26996948	PCS		2/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0003593	PMID:26996948	PCS		4/5			C	HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001290	PMID:26996948	PCS	HP:0003577				P	HPO:probinson[2017-06-24]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0011193	PMID:26996948	PCS					P	HPO:probinson[2017-06-24]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0011461	PMID:26996948	PCS		1/5			C	HPO:probinson[2022-03-05]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0000007	PMID:26996948	PCS					I	HPO:probinson[2017-06-24]
OMIM:616917	Neurodevelopmental disorder with or without hypotonia, seizures, and cerebellar atrophy		HP:0001511	PMID:26996948	PCS		1/5			P	HPO:probinson[2017-06-24];HPO:probinson[2022-03-05]
OMIM:301050	Alport syndrome, X-linked		HP:0003774	OMIM:301050	TAS					P	HPO:skoehler[2012-11-26]
OMIM:301050	Alport syndrome, X-linked		HP:0003676	OMIM:301050	TAS					C	HPO:skoehler[2012-10-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000123	OMIM:301050	IEA					P	HPO:skoehler[2010-06-20]
OMIM:301050	Alport syndrome, X-linked		HP:0000100	OMIM:301050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000083	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:6001026	PMID:22921432	PCS		183/207			P	HPO:probinson[2024-08-03]
OMIM:301050	Alport syndrome, X-linked		HP:0001142	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0030034	OMIM:301050	TAS					P	HPO:skoehler[2014-09-21]
OMIM:301050	Alport syndrome, X-linked		HP:0011501	OMIM:301050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000093	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000829	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0008064	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000407	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0002907	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000519	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000822	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0001417	OMIM:301050	IEA					I	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0001423	OMIM:301050	TAS					I	HPO:skoehler[2013-05-29]
OMIM:301050	Alport syndrome, X-linked		HP:0001873	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0200020	OMIM:301050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301050	Alport syndrome, X-linked		HP:0000545	OMIM:301050	TAS					P	HPO:skoehler[2012-10-17]
OMIM:301050	Alport syndrome, X-linked		HP:0006756	OMIM:301050	IEA					P	HPO:iea[2009-02-17]
OMIM:301050	Alport syndrome, X-linked		HP:0004722	OMIM:301050	TAS					P	HPO:skoehler[2015-12-30]
OMIM:618084	Peeling skin syndrome 6		HP:0003577	PMID:28884927	PCS		1/1			C	HPO:probinson[2023-02-22]
OMIM:618084	Peeling skin syndrome 6		HP:0001036	OMIM:618084	IEA					P	HPO:skoehler[2018-10-08]
OMIM:618084	Peeling skin syndrome 6		HP:0001047	PMID:28884927	PCS		3/3			P	HPO:probinson[2023-02-22]
OMIM:618084	Peeling skin syndrome 6		HP:0000958	PMID:28884927	PCS		3/3			P	HPO:probinson[2023-02-22]
OMIM:618084	Peeling skin syndrome 6		HP:0040189	PMID:28884927	PCS		3/3			P	HPO:probinson[2023-02-22];HPO:probinson[2023-02-22]
OMIM:618084	Peeling skin syndrome 6		HP:0000007	PMID:28884927	PCS					I	HPO:skoehler[2019-04-18];HPO:probinson[2023-02-22]
OMIM:618084	Peeling skin syndrome 6		HP:0000989	OMIM:618084	IEA		3/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:618084	Peeling skin syndrome 6		HP:0040162	PMID:28884927	PCS		1/1			P	HPO:skoehler[2018-10-08];HPO:probinson[2023-02-22]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0004963	OMIM:208060	TAS					P	HPO:probinson[2012-04-06]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0004589	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0001385	OMIM:208060	TAS					P	HPO:probinson[2012-04-06]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0004322	OMIM:208060	TAS					P	HPO:probinson[2012-04-06]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0002592	OMIM:208060	IEA					P	HPO:skoehler[2018-10-08]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0012622	OMIM:208060	TAS					P	HPO:probinson[2014-01-18]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0001903	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0008014	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0000822	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0001658	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0000007	OMIM:208060	IEA					I	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0030053	OMIM:208060	TAS					P	HPO:probinson[2022-07-01]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0000823	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0002634	OMIM:208060	TAS					P	HPO:probinson[2012-04-06]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0009803	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:208060	Arteriosclerosis, severe juvenile		HP:0007768	OMIM:208060	IEA					P	HPO:probinson[2009-02-17]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000286	PMID:14630978	PCS		1/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001254	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0007759	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000365	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001250	PMID:14630978	PCS		2/4			P	HPO:probinson[2013-02-24];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0003155	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001252	PMID:14630978	PCS		3/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0033643	PMID:14630978	PCS		3/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001093	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000518	PMID:14630978	PCS		1/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0011463	PMID:14630978	PCS		1/4			C	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0010571	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000316	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000239	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000954	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001522	PMID:14630978	PCS		2/4			C	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001401	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000510	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001840	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000113	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000311	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001249	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000952	PMID:14630978	PCS		1/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0003623	PMID:14630978	PCS		1/4			C	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000175	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0031956	PMID:14630978	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0030148	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002197	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002033	PMID:14630978	PCS		1/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001263	OMIM:614866	TAS					P	HPO:probinson[2013-02-24]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0030948	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0031358	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0005180	PMID:14630978	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0100540	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0012385	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002908	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000407	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000007	PMID:1546315	PCS					I	HPO:probinson[2013-02-24];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000648	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001659	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002305	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000047	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001653	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000369	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001396	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0003577	PMID:14630978	PCS		1/4			C	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001792	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001272	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000260	PMID:14630978	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001274	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002240	PMID:14630978	PCS		2/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000580	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0011039	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0012368	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0031964	PMID:14630978	PCS		2/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001508	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001629	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0008872	OMIM:614866	TAS					P	HPO:probinson[2013-02-24]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0025116	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000218	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0025435	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002557	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001302	OMIM:614866;PMID:14630978	PCS		11/14			P	HPO:probinson[2023-02-10];HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0004734	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001744	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0006855	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001088	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001762	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001321	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0030048	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0004474	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001284	PMID:14630978	PCS		2/4			P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0011421	PMID:14630978	PCS		1/4			C	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0010655	OMIM:614866	TAS					P	HPO:probinson[2013-02-24]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001518	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0012043	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000107	OMIM:614866	TAS					P	HPO:probinson[2013-02-24]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000348	OMIM:614866;PMID:14630978	PCS		11/14			P	HPO:probinson[2023-02-10];HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0008665	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002967	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001511	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001631	PMID:14630978	PCS		1/4			P	HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0001433	OMIM:614866	TAS					P	HPO:probinson[2013-02-24]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000028	PMID:14630978	PCS		1/3	MALE		P	HPO:skoehler[2015-08-16];HPO:probinson[2023-02-10]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0000347	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002126	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:614866	Peroxisome biogenesis disorder 5A (Zellweger)		HP:0002764	OMIM:614866	TAS					P	HPO:skoehler[2015-08-16]
OMIM:188800	Tibial torsion, bilateral medial		HP:0002650	OMIM:188800	IEA					P	HPO:skoehler[2018-10-08]
OMIM:188800	Tibial torsion, bilateral medial		HP:0002979	OMIM:188800	TAS					P	HPO:probinson[2012-07-19]
OMIM:188800	Tibial torsion, bilateral medial		HP:0000006	OMIM:188800	TAS					I	HPO:iea[2009-02-17]
OMIM:188800	Tibial torsion, bilateral medial		HP:0100694	OMIM:188800	TAS					P	HPO:skoehler[2012-10-17]
OMIM:187500	Tetralogy of Fallot		HP:0004467	OMIM:187500	IEA					P	HPO:iea[2009-02-17]
OMIM:187500	Tetralogy of Fallot		HP:0001636	OMIM:187500	IEA					P	HPO:iea[2009-02-17]
OMIM:187500	Tetralogy of Fallot		HP:0000337	OMIM:187500	IEA					P	HPO:iea[2009-02-17]
OMIM:187500	Tetralogy of Fallot		HP:0004209	OMIM:187500	IEA					P	HPO:iea[2009-02-17]
OMIM:187500	Tetralogy of Fallot		HP:0000520	OMIM:187500	IEA					P	HPO:iea[2009-02-17]
OMIM:187500	Tetralogy of Fallot		HP:0000006	OMIM:187500	IEA					I	HPO:iea[2009-02-17]
OMIM:151620	Lichen planus, familial		HP:0000006	OMIM:151620	IEA					I	HPO:iea[2009-02-17]
OMIM:151620	Lichen planus, familial		HP:0000951	OMIM:151620	IEA					P	HPO:iea[2009-02-17]
OMIM:616042	Deafness, autosomal recessive 103		HP:0001751	PMID:24781754	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-08]
OMIM:616042	Deafness, autosomal recessive 103		HP:0000407	PMID:24781754	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-08]
OMIM:616042	Deafness, autosomal recessive 103		HP:0011463	PMID:24781754	PCS		2/2			C	HPO:probinson[2022-11-08]
OMIM:616042	Deafness, autosomal recessive 103		HP:0000007	PMID:24781754	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2022-11-08]
OMIM:616042	Deafness, autosomal recessive 103		HP:0008568	PMID:24781754	PCS		2/2			P	HPO:skoehler[2014-11-26];HPO:probinson[2022-11-08]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0031329	PMID:32514796	PCS		2/2			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0030149	PMID:32514796	PCS	HP:0003593	1/6			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0003593	PMID:32514796;PMID:32870709	PCS		9/12			C	HPO:probinson[2022-07-04];HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0030718	PMID:32514796	PCS		1/6			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0002092	PMID:32514796	PCS		3/5			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0012664	PMID:32514796	PCS		5/5			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0033997	PMID:32514796	PCS		2/2			P	HPO:probinson[2021-10-03]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0005180	PMID:32514796	PCS		3/5			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0011623	PMID:32514796	PCS		1/5			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0000007	PMID:32514796	PCS					I	HPO:probinson[2021-08-18];HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0001522	PMID:32514796	PCS		4/6			C	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0001653	PMID:32514796	PCS		3/5			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0001644	PMID:32514796	PCS	HP:0003593	6/6			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0001655	PMID:32514796	PCS		1/5			P	HPO:probinson[2021-08-18]
OMIM:619371	Cardiomyopathy, dilated, 2D		HP:0003623	PMID:32514796	PCS		3/6			C	HPO:probinson[2021-08-18]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0003301	PMID:17726487	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0002650	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0001376	PMID:17726487	PCS		5/5			P	HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0001371	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0008819	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0030431	PMID:17726487	PCS		3/5			P	HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0003370	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0010049	PMID:17726487	PCS		2/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0010743	PMID:17726487	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0100864	OMIM:609162	TAS					P	HPO:probinson[2012-06-08]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0002829	PMID:17726487	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0001507	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0000926	PMID:17726487	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0002812	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0002515	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0002945	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0002868	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0002942	OMIM:609162	IEA					P	HPO:iea[2009-02-17]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0000006	PMID:17726487	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-10-13]
OMIM:609162	Czech dysplasia, Metatarsal type		HP:0001831	PMID:17726487	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2021-10-13]
OMIM:616724	Tooth agenesis, selective, 7		HP:0000679	PMID:26387593	PCS		6/28			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-03-15]
OMIM:616724	Tooth agenesis, selective, 7		HP:0000006	PMID:26387593	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-15]
OMIM:616724	Tooth agenesis, selective, 7		HP:0006349	PMID:26387593	PCS		20/26			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-03-15]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003376	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0000365	OMIM:118220	TAS					P	HPO:skoehler[2012-11-16]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003431	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0001178	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003693	OMIM:118220	TAS					P	HPO:probinson[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0002460	OMIM:118220	TAS					P	HPO:probinson[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003690	OMIM:118220	TAS					P	HPO:skoehler[2012-11-16]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0001171	OMIM:118220	TAS					P	HPO:skoehler[2015-12-30]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003828	OMIM:118220	TAS					M	HPO:skoehler[2012-10-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0009027	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0002936	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003449	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0001765	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0004336	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0002751	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003587	OMIM:118220	IEA					C	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0001265	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003621	OMIM:118220	IEA					C	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0001761	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003383	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0001284	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003481	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003382	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003380	OMIM:118220	IEA					P	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0009830	OMIM:118220	TAS					P	HPO:skoehler[2012-11-18]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0003677	OMIM:118220	IEA					C	HPO:iea[2009-02-17]
OMIM:118220	Charcot-Marie-Tooth disease, demyelinating, type 1A		HP:0000006	OMIM:118220	IEA					I	HPO:iea[2009-02-17]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0006515	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0200029	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0001903	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0000979	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0002240	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0000967	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0002878	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0002788	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0002091	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0000006	PMID:34536415	PCS					I	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0001744	PMID:34536415	PCS		1/1			P	HPO:probinson[2023-06-24]
OMIM:620296	Autoinflammation with pulmonary and cutaneous vasculitis		HP:0003623	PMID:34536415	PCS		1/1			C	HPO:probinson[2023-06-24]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0000252	PMID:31353024	PCS		2/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0001250	PMID:31353024	PCS		6/14			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0001263	PMID:31353024	IEA		12/14			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0001252	PMID:31353024	PCS		6/14			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0001251	PMID:31353024	PCS		4/14			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0001273	PMID:31353024	PCS		6/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0012443	PMID:31353024	PCS		11/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0000729	PMID:31353024	PCS		6/14			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0002539	PMID:31353024	PCS		3/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0001999	PMID:31353024	PCS		8/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0000733	PMID:31353024	PCS		4/14			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0000238	PMID:31353024	PCS		3/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0002119	PMID:31353024	PCS		8/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0007018	PMID:31353024	PCS		3/14			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0000256	PMID:31353024	PCS		1/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0000006	PMID:31353024	PCS					I	HPO:probinson[2020-07-07];HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0001249	PMID:31353024	PCS					P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0002269	PMID:31353024	PCS		1/15			P	HPO:probinson[2020-07-07]
OMIM:618709	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures		HP:0003468	PMID:31353024	PCS		4/15			P	HPO:probinson[2020-07-07]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0003577	PMID:11528396	PCS		11/11			C	HPO:probinson[2022-10-06]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0003693	OMIM:604320	TAS					P	HPO:probinson[2012-04-11]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0100490	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0000020	OMIM:604320	TAS					P	HPO:probinson[2012-04-11]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0002460	OMIM:604320	TAS					P	HPO:probinson[2012-04-11]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0003690	OMIM:604320	TAS					P	HPO:probinson[2012-04-11]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001508	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0040078	OMIM:604320	IEA					P	HPO:skoehler[2018-10-08]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0000975	OMIM:604320	TAS					P	HPO:probinson[2012-04-11]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0006597	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0002878	OMIM:604320	TAS					P	HPO:skoehler[2014-06-24]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0007269	PMID:11528396	PCS					P	HPO:probinson[2012-04-11];HPO:probinson[2022-10-06]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0005946	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0002019	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0009109	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001622	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001265	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0005348	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0003445	OMIM:604320	TAS					P	HPO:probinson[2012-04-11]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001762	PMID:11528396	PCS		1/11			P	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0002398	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0009110	PMID:11528396	PCS		11/11			P	HPO:probinson[2012-04-11];HPO:probinson[2022-10-06]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001518	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0009113	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0000007	PMID:11528396	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-10-06]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001558	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001319	PMID:11528396	PCS		11/11			P	HPO:probinson[2022-10-06]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001511	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0000762	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0002789	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0001612	OMIM:604320	IEA					P	HPO:iea[2009-02-17]
OMIM:604320	Spinal muscular atrophy, distal, autosomal recessive, 1		HP:0000764	OMIM:604320	TAS					P	HPO:probinson[2012-04-11]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001331	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000286	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0003577	PMID:15642837;PMID:12796275	PCS		2/2			C	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000365	PMID:15642837;PMID:12796275	PCS		2/2			P	HPO:probinson[2022-08-17];HPO:probinson[2022-08-17];HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0002002	OMIM:613884	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000023	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0009919	PMID:12796275	PCS	HP:0003593	1/1			P	HPO:skoehler[2012-10-17];HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0009919	PMID:15642837	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001274	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0040080	OMIM:613884	TAS					P	HPO:skoehler[2014-11-26]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001629	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001845	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000954	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000337	OMIM:613884	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000414	OMIM:613884	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000612	PMID:15642837	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000219	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000218	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0003745	OMIM:613884	TAS					I	HPO:skoehler[2015-12-30]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0002558	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001249	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0008936	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000054	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000750	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000232	OMIM:613884	TAS					P	HPO:skoehler[2013-01-22]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0002079	OMIM:613884	TAS		HP:0040283			P	HPO:skoehler[2012-11-18]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001360	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0002827	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001537	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000601	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000568	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0004209	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000268	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0002007	OMIM:613884	TAS					P	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001510	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000006	OMIM:613884	TAS					I	HPO:skoehler[2012-10-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000567	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000028	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000369	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0000347	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:613884	Chromosome 13q14 deletion syndrome		HP:0001655	PMID:12796275	PCS		1/1			P	HPO:probinson[2022-08-17]
OMIM:616730	Nephrotic syndrome, type 11		HP:0003774	PMID:26411495	PCS					P	HPO:probinson[2017-06-17]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000341	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0003676	OMIM:616730	TAS					C	HPO:skoehler[2017-07-13]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000340	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000100	PMID:26411495	PCS					P	HPO:probinson[2017-06-17]
OMIM:616730	Nephrotic syndrome, type 11		HP:0003073	PMID:26411495	PCS					P	HPO:probinson[2017-06-17]
OMIM:616730	Nephrotic syndrome, type 11		HP:0410030	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0001629	OMIM:616730	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000319	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0003828	OMIM:616730	TAS					M	HPO:skoehler[2017-07-13]
OMIM:616730	Nephrotic syndrome, type 11		HP:0001967	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000218	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0030084	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0009944	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0001644	OMIM:616730	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0001166	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000175	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000794	OMIM:616730	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000750	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0003124	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000097	PMID:26411495	PCS		8/10			P	HPO:probinson[2017-06-17]
OMIM:616730	Nephrotic syndrome, type 11		HP:0001263	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000093	PMID:26411495	PCS					P	HPO:probinson[2017-06-17]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000092	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0012579	OMIM:616730	TAS					P	HPO:skoehler[2017-07-13]
OMIM:616730	Nephrotic syndrome, type 11		HP:0001999	OMIM:616730	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000007	PMID:26411495	PCS					I	HPO:probinson[2017-06-17]
OMIM:616730	Nephrotic syndrome, type 11		HP:0000347	OMIM:616730	IEA					P	HPO:skoehler[2019-02-22]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0003621	PMID:30872117	PCS		1/2			C	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0002155	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0002783	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0020072	PMID:30872117	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0002110	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0410295	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0011900	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0011108	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0012189	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0012476	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0031382	PMID:30872117	PCS		2/2			P	HPO:probinson[2023-07-09];HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0011463	PMID:30872117	PCS		1/2			C	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0030252	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0000007	PMID:30872117	PCS					I	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0008940	PMID:30872117	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0001744	PMID:30872117	PCS		2/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0001876	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:620282	Immunodeficiency 109 with lymphoproliferation		HP:0004315	PMID:30872117	PCS		1/2			P	HPO:probinson[2023-07-09]
OMIM:234000	Factor XII deficiency		HP:0004841	OMIM:234000	IEA					P	HPO:iea[2009-02-17]
OMIM:234000	Factor XII deficiency		HP:0005542	OMIM:234000	IEA					P	HPO:iea[2009-02-17]
OMIM:234000	Factor XII deficiency		HP:0000007	OMIM:234000	IEA					I	HPO:iea[2009-02-17]
OMIM:234000	Factor XII deficiency		HP:0003645	OMIM:234000	IEA					P	HPO:iea[2009-02-17]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0000486	OMIM:610427	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0000551	OMIM:610427	TAS		HP:0040283			P	HPO:skoehler[2015-05-31]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0000639	PMID:16960802	PCS					P	HPO:probinson[2013-02-28]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0000613	OMIM:610427	TAS					P	HPO:skoehler[2015-05-31]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0000007	PMID:16960802	PCS					I	HPO:probinson[2013-02-28]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0007642	PMID:16960802	PCS					P	HPO:probinson[2013-02-28]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0000505	PMID:16960802	PCS					P	HPO:probinson[2013-02-28]
OMIM:610427	Cone-Rod synaptic disorder, congenital nonprogressive		HP:0007984	PMID:16960802	PCS					P	HPO:probinson[2013-03-12]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0002069	PMID:25164438	PCS		3/3			P	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0002521	PMID:25164438	PCS		1/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0001344	PMID:25164438	PCS		1/3			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0002384	PMID:25164438	PCS		1/3			P	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0010819	PMID:25164438	PCS		3/3			P	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0001263	PMID:25164438	PCS		3/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0001252	PMID:25164438	PCS		2/3			P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0003593	PMID:25164438	PCS		1/3			C	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0012469	PMID:25164438	PCS		2/3			P	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0007270	PMID:25164438	PCS		1/3			P	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0011463	PMID:25164438	PCS		1/3			C	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0200134	PMID:25164438	PCS					P	HPO:skoehler[2014-11-26];HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0007334	PMID:25164438	PCS		1/3			P	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0012171	PMID:25164438	PCS		1/3			P	HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0000006	PMID:25164438	PCS					I	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-16]
OMIM:616056	Developmental and epileptic encephalopathy 26		HP:0003623	PMID:25164438	PCS		1/3			C	HPO:probinson[2021-02-16]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0001562	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0000010	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0000021	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0012762	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0010945	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0000007	PMID:33031641	PCS					I	HPO:probinson[2021-07-08];HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0011499	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0003270	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0002205	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0000787	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:619365	Megacystis-microcolon-intestinal hypoperistalsis syndrome 4		HP:0100771	PMID:33031641	PCS		1/1			P	HPO:probinson[2021-07-08]
OMIM:614899	Deafness, autosomal recessive 93		HP:0003577	PMID:22981119	PCS					C	HPO:probinson[2022-09-30]
OMIM:614899	Deafness, autosomal recessive 93		HP:0000365	PMID:22981119	PCS					P	HPO:skoehler[2015-01-27];HPO:probinson[2022-09-30]
OMIM:614899	Deafness, autosomal recessive 93		HP:0000007	PMID:22981119	PCS					I	HPO:skoehler[2012-11-16];HPO:probinson[2022-09-30]
OMIM:247950	Lysine malabsorption syndrome		HP:0008272	OMIM:247950	IEA					P	HPO:iea[2009-02-17]
OMIM:247950	Lysine malabsorption syndrome		HP:0003297	OMIM:247950	IEA					P	HPO:iea[2009-02-17]
OMIM:247950	Lysine malabsorption syndrome		HP:0000007	OMIM:247950	IEA					I	HPO:iea[2009-02-17]
OMIM:247950	Lysine malabsorption syndrome		HP:0001510	OMIM:247950	IEA					P	HPO:iea[2009-02-17]
OMIM:247950	Lysine malabsorption syndrome		HP:0001249	OMIM:247950	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0003510	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001276	PMID:18524657	PCS		3/111			P	HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000023	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001250	PMID:18524657	PCS		10/115			P	HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001252	PMID:18524657;PMID:22234367	PCS		111/115			P	HPO:probinson[2022-04-30];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0010729	PMID:18524657	PCS		50/84			P	HPO:skoehler[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0002240	PMID:18524657	PCS		104/122			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0003593	PMID:22234367	PCS		4/4			C	HPO:probinson[2022-04-30]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000280	OMIM:230500	IEA		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001071	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000316	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000998	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001922	PMID:18524657	PCS					P	HPO:iea[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001789	PMID:18524657	PCS		8/130			P	HPO:probinson[2021-07-01];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0008479	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001522	OMIM:230500	IEA					C	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000212	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000457	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001249	PMID:18524657;PMID:22234367	PCS		119/119			P	HPO:probinson[2022-04-30];HPO:iea[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001744	PMID:18524657	PCS		104/122			P	HPO:iea[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001644	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000079	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0002650	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001387	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001263	PMID:18524657;PMID:22234367	PCS		119/119			P	HPO:probinson[2022-04-30];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000470	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001639	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0002808	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0008166	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000943	PMID:22234367	PCS		4/4			P	HPO:probinson[2022-04-30]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000007	PMID:18524657	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001635	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0007313	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0000900	OMIM:230500	TAS					P	HPO:probinson[2012-07-16]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001654	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0002007	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:230500	GM1-gangliosidosis, type I		HP:0001511	PMID:18524657	PCS	HP:0011461	2/130			P	HPO:probinson[2021-07-01]
OMIM:230500	GM1-gangliosidosis, type I		HP:0004568	OMIM:230500	IEA					P	HPO:iea[2009-02-17]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0000662	PMID:33602140	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0030498	PMID:33602140	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0012026	PMID:33602140;PMID:3339136	PCS		3/3			P	HPO:probinson[2022-04-30]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0011463	PMID:33602140	PCS		1/1			C	HPO:probinson[2022-04-30]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0012152	PMID:33602140	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0000618	OMIM:258870	IEA					P	HPO:iea[2009-02-17]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0000007	PMID:2916580	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0000505	PMID:33602140	PCS		1/1			P	HPO:probinson[2022-04-30]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0003701	OMIM:258870	IEA					P	HPO:iea[2009-02-17]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0007787	OMIM:258870	IEA					P	HPO:iea[2009-02-17]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0000545	OMIM:258870	IEA					P	HPO:iea[2009-02-17]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0003457	OMIM:258870	IEA					P	HPO:iea[2009-02-17]
OMIM:258870	Gyrate atrophy of choroid and retina with or without ornithinemia		HP:0000533	PMID:33602140	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2022-04-30]
OMIM:306930	Hemopoietic proliferation		HP:0001871	OMIM:306930	IEA					P	HPO:iea[2009-02-17]
OMIM:306930	Hemopoietic proliferation		HP:0001417	OMIM:306930	IEA					I	HPO:iea[2009-02-17]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000286	PMID:27479907	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000486	PMID:27479907	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000200	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0004322	PMID:27479907	PCS		2/5			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001250	OMIM:617360	IEA		HP:0040284			P	HPO:skoehler[2019-02-22]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000160	PMID:27479907	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001252	PMID:27479907	PCS		3/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002020	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0012745	OMIM:617360	IEA					P	HPO:skoehler[2019-02-22]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0011856	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000319	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000717	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000316	PMID:27479907	PCS		4/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0025336	PMID:27479907	PCS		6/6			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000356	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002019	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000358	PMID:27479907	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001249	PMID:27479907	PCS		5/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002553	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000252	PMID:27479907	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000574	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002079	PMID:27479907	PCS		1/7			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002472	OMIM:617360	TAS		HP:0040283			P	HPO:skoehler[2017-07-13]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001382	PMID:27479907	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0011968	PMID:27479907	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000691	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001263	PMID:27479907	PCS		7/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0012385	PMID:27479907	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000322	PMID:27479907	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000369	PMID:27479907	PCS		1/7			P	HPO:skoehler[2019-02-22];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000006	PMID:27479907	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000324	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000582	PMID:27479907	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0003577	PMID:27479907	PCS		7/7			C	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002121	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0003298	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002162	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000581	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001274	PMID:27479907	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001270	PMID:27479907	PCS		5/5			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001629	PMID:27479907	PCS		3/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000414	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0006970	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000219	PMID:27479907	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002714	PMID:27479907	PCS		2/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0030084	PMID:27479907	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0006610	PMID:27479907	PCS		2/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0005989	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000215	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000396	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002212	PMID:27479907	PCS		1/7			P	HPO:skoehler[2019-04-18];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001561	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000431	PMID:27479907	PCS		2/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000233	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000750	PMID:27479907	PCS		4/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002650	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0031936	PMID:27479907	PCS		5/5			P	HPO:skoehler[2018-10-08];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0002572	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0010536	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000506	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000508	PMID:27479907	PCS		1/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000426	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001357	PMID:27479907	PCS		2/14			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0007413	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001511	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0001631	PMID:27479907	PCS		5/7			P	HPO:skoehler[2017-07-13];HPO:probinson[2022-09-25]
OMIM:617360	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		HP:0000269	PMID:27479907	PCS		1/7			P	HPO:probinson[2022-09-25]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0005215	PMID:24140114	PCS		2/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0007418	PMID:24140114	PCS		2/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0002021	PMID:24140114	PCS		1/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0011734	PMID:24140114	PCS		4/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0012203	PMID:24140114	PCS		1/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0031074	PMID:24140114	PCS		2/2			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0011463	PMID:24140114	PCS		4/4			C	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0001943	PMID:24140114	PCS					P	HPO:skoehler[2018-10-08];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0006532	PMID:24140114	PCS		3/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0003765	PMID:24140114	PCS		1/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0410028	PMID:24140114	PCS		3/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0004315	PMID:24140114	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0002850	PMID:24140114	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0025379	PMID:24140114	PCS		2/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0002099	PMID:24140114	PCS		4/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0005387	PMID:24140114	PCS		4/4			P	HPO:probinson[2021-05-09];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0001263	PMID:24140114	PCS		1/4			P	HPO:skoehler[2014-03-24];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0032069	PMID:24140114	PCS		1/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0030804	PMID:24140114	PCS		2/4			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0011108	PMID:24140114	PCS		3/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0007099	PMID:24140114	PCS		2/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0033166	PMID:24140114	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0000403	PMID:24140114	PCS		3/4			P	HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0000824	OMIM:615577	TAS		HP:0040283			P	HPO:skoehler[2015-04-05]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0000006	PMID:24140114	PCS					I	HPO:skoehler[2014-03-24];HPO:probinson[2021-05-09]
OMIM:615577	Immunodeficiency, common variable, 10		HP:0002720	PMID:24140114	PCS		4/4			P	HPO:probinson[2021-05-09]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000365	PMID:16114046	PCS		4/19			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000160	PMID:16114046	PCS		14/27			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0025267	OMIM:614669	TAS					P	HPO:skoehler[2017-07-13]
OMIM:614669	Auriculocondylar syndrome 2		HP:0001252	PMID:16114046	PCS		2/11			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000162	PMID:16114046	PCS		5/11			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0009088	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0011342	PMID:16114046	PCS		3/13			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000678	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000256	PMID:16114046	PCS		3/12			P	HPO:skoehler[2012-11-18];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000311	PMID:16114046	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000358	PMID:16114046	PCS		2/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0008537	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0008559	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000175	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0007627	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0007628	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0004453	PMID:16114046	PCS					P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0002098	PMID:16114046	PCS		8/22			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0011968	PMID:16114046	PCS		4/19			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000171	PMID:16114046	PCS		2/11			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0012478	PMID:16114046	PCS		1/20			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000508	PMID:16114046	PCS		3/11			P	HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000007	OMIM:614669	TAS					I	HPO:skoehler[2013-10-06]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000689	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0003778	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0002104	OMIM:614669	TAS					P	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000006	OMIM:614669	TAS					I	HPO:skoehler[2012-10-17]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000369	PMID:16114046	PCS		2/20			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000347	PMID:16114046	PCS		22/31			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-01-30]
OMIM:614669	Auriculocondylar syndrome 2		HP:0000402	PMID:16114046	PCS		3/10			P	HPO:probinson[2023-01-30]
OMIM:613660	Cone-rod dystrophy 15		HP:0001133	PMID:20805371	PCS					P	HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0000662	PMID:20805371	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0000551	PMID:20805371	PCS					P	HPO:skoehler[2013-05-29];HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0000529	PMID:20805371	PCS		6/6			P	HPO:skoehler[2013-05-31];HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0000613	PMID:20805371	PCS		HP:0040283			P	HPO:skoehler[2012-11-18];HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0000007	PMID:20805371	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0000510	PMID:20805371	PCS					P	HPO:skoehler[2015-01-19];HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0007722	PMID:20805371	PCS					P	HPO:probinson[2021-06-01]
OMIM:613660	Cone-rod dystrophy 15		HP:0007843	PMID:20805371	PCS					P	HPO:probinson[2021-06-01]
OMIM:268025	Retinitis pigmentosa, late-adult onset		HP:0000007	OMIM:268025	IEA					I	HPO:iea[2009-02-17]
OMIM:268025	Retinitis pigmentosa, late-adult onset		HP:0000510	OMIM:268025	IEA	HP:0003584				P	HPO:iea[2009-02-17]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0002289	PMID:20302578;PMID:16175511	PCS		3/3			P	HPO:skoehler[2015-12-30];HPO:probinson[2021-02-21];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0007418	PMID:20613772	PCS		1/1			P	HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0000695	PMID:16175511	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0001057	PMID:16175511	PCS		1/1			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0004057	PMID:16175511	PCS		1/1			P	HPO:skoehler[2014-01-28];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0100792	PMID:20302578;PMID:20613772;PMID:16175511	PCS		4/4			P	HPO:probinson[2021-02-21];HPO:probinson[2013-03-22];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0008094	PMID:16175511	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0008066	PMID:20613772	PCS		1/1			P	HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0001817	PMID:20613772	PCS		1/1			P	HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0009884	PMID:16175511	PCS		1/1			P	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0000007	PMID:16175511	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0004209	PMID:20302578	PCS		1/2			P	HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0001159	PMID:20302578	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0001852	PMID:16175511	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0003811	PMID:20302578;PMID:20613772;PMID:16175511	PCS		4/4			C	HPO:iea[2009-02-17];HPO:probinson[2021-02-21];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0200041	PMID:20302578;PMID:16175511	PCS		3/3			P	HPO:probinson[2021-02-21];HPO:skoehler[2010-06-20];HPO:probinson[2021-02-21]
OMIM:609638	Epidermolysis bullosa, lethal acantholytic		HP:0001798	PMID:16175511	PCS		1/1			P	HPO:skoehler[2015-02-22];HPO:probinson[2021-02-21]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0001133	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000164	OMIM:617406	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000750	PMID:26854863	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0030631	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0001162	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000085	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0030329	PMID:26854863	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000618	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0007750	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0030483	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000668	OMIM:617406	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000007	PMID:27008867	PCS					I	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0025502	OMIM:617406	IEA					P	HPO:skoehler[2019-09-07]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000548	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000510	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0002910	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0001513	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0000545	OMIM:617406	IEA					P	HPO:skoehler[2018-10-08]
OMIM:617406	Bardet-Biedl syndrome 21		HP:0001105	PMID:27008867	PCS					P	HPO:probinson[2017-05-30]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0000253	PMID:31422819	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0001320	PMID:31422819	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0004325	PMID:31422819	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0002059	PMID:31422819	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0002510	PMID:31422819	PCS		2/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0001344	PMID:31422819	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0000750	PMID:31422819	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0002540	PMID:31422819	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0002079	PMID:31422819	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0004322	PMID:31422819	PCS		3/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0001250	PMID:31422819	PCS	HP:0003593	4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0002151	PMID:31422819	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0002719	PMID:31422819	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0000007	PMID:31422819	PCS					I	HPO:probinson[2020-05-11];HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0008872	PMID:31422819	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0001987	PMID:31422819	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0001319	PMID:31422819	PCS		4/4			P	HPO:probinson[2020-05-11]
OMIM:618721	Epileptic encephalopathy, early infantile, 82		HP:0002313	PMID:31422819	PCS		2/4			P	HPO:probinson[2020-05-11]
OMIM:150270	Laryngeal adductor paralysis		HP:0001609	OMIM:150270	TAS	HP:0003577				P	HPO:iea[2009-02-17]
OMIM:150270	Laryngeal adductor paralysis		HP:0003470	OMIM:150270	IEA					P	HPO:skoehler[2018-10-08]
OMIM:150270	Laryngeal adductor paralysis		HP:0000006	PMID:709905	PCS					I	HPO:iea[2009-02-17]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000286	PMID:28257692	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0001212	PMID:28257692	PCS		2/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0004322	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0001290	PMID:28257692	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0001270	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000954	PMID:28257692	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0001328	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000218	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000179	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0005469	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0002553	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000176	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000396	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000252	PMID:28257692	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000574	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000233	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0002299	PMID:28257692	PCS		1/2			P	HPO:skoehler[2018-10-08];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000194	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000193	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000592	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0011069	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0005280	PMID:28257692	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000729	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000629	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000527	PMID:28257692	PCS		2/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000405	PMID:28257692	PCS					P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000664	PMID:28257692	PCS		1/2			P	HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000006	PMID:28257692	PCS					I	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:617412	Brachycephaly, trichomegaly, and developmental delay		HP:0000369	PMID:28257692	PCS		1/2			P	HPO:skoehler[2017-07-13];HPO:probinson[2021-04-25]
OMIM:604308	Mass syndrome		HP:0001166	PMID:21332468	PCS		4/4			P	HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0002650	PMID:21332468	PCS		1/4			P	HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0100775	PMID:21332468	PCS		3/4			P	HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0001519	PMID:21332468	PCS		3/3			P	HPO:skoehler[2013-02-23];HPO:probinson[2021-04-25];HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0001065	PMID:21332468	PCS		5/7			P	HPO:skoehler[2013-02-23];HPO:probinson[2021-04-25];HPO:probinson[2022-03-13];HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0001083	PMID:21332468	PCS		0/3			P	HPO:skoehler[2013-02-23];HPO:probinson[2021-04-25];HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0000768	PMID:21332468	PCS		1/4			P	HPO:probinson[2021-04-25];HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0004933	PMID:21332468	PCS		0/7			P	HPO:probinson[2021-04-25];HPO:probinson[2022-03-13];HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0000006	PMID:21332468	PCS					I	HPO:skoehler[2013-01-09];HPO:probinson[2021-04-25]
OMIM:604308	Mass syndrome		HP:0001634	PMID:21332468	PCS		3/3			P	HPO:skoehler[2013-02-23];HPO:probinson[2021-04-25];HPO:probinson[2022-03-13]
OMIM:604308	Mass syndrome		HP:0004942	PMID:21332468	PCS		7/7		HP:0012825;HP:0012825	P	HPO:skoehler[2013-02-23];HPO:probinson[2021-04-25];HPO:probinson[2022-03-13];HPO:probinson[2022-03-13]
OMIM:613674	Vesicoureteral reflux 3		HP:0012572	PMID:20960469	PCS		2/4			P	HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0000010	PMID:20960469	PCS		1/4			P	HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0001561	PMID:20960469	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0033737	PMID:20960469	PCS		1/4			P	HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0000072	PMID:20960469	PCS		1/4			P	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0000074	PMID:20960469	PCS		1/4			P	HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0012450	PMID:20960469	PCS		2/4			P	HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0033741	PMID:20960469	PCS		1/4			P	HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0000006	PMID:20960469	PCS					I	HPO:skoehler[2012-10-17];HPO:probinson[2023-03-11]
OMIM:613674	Vesicoureteral reflux 3		HP:0000126	PMID:20960469	PCS		2/4			P	HPO:skoehler[2012-10-17]
OMIM:603467	Fanconi anemia, complementation group F		HP:0003577	PMID:27714961	PCS		3/3			C	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0011419	PMID:27714961	PCS	HP:0011461	1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0004322	PMID:31288759;PMID:27714961	PCS		3/4			P	HPO:probinson[2021-07-05];HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001233	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000089	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001195	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001508	PMID:31288759	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001903	PMID:31288759	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000957	PMID:27714961	PCS		3/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0008551	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001328	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000953	PMID:31288759	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0030260	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0005528	PMID:31288759	PCS		1/1			P	HPO:probinson[2013-09-14];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001643	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000252	PMID:31288759;PMID:27714961	PCS		2/4			P	HPO:probinson[2021-07-05];HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001561	PMID:27714961	PCS	HP:0011461	1/3			P	HPO:probinson[2021-07-05];HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000076	PMID:27714961	PCS		2/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000750	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001882	PMID:31288759	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0003221	PMID:31288759	PCS		1/1			P	HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0002090	PMID:31288759	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000007	PMID:10615118	PCS					I	HPO:probinson[2013-09-14];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000568	PMID:27714961	PCS		2/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0009777	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000824	PMID:27714961	PCS		2/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000405	PMID:27714961	PCS		2/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001511	PMID:27714961	PCS	HP:0011461	1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000125	PMID:27714961	PCS		2/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001873	PMID:31288759	PCS		1/1			P	HPO:probinson[2020-07-22];HPO:probinson[2020-07-22]
OMIM:603467	Fanconi anemia, complementation group F		HP:0009778	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000960	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0001631	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0002984	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0002247	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:603467	Fanconi anemia, complementation group F		HP:0000028	PMID:27714961	PCS		1/3			P	HPO:probinson[2021-07-05]
OMIM:613112	Macrothrombocytopenia, autosomal dominant, tubb1-related		HP:0003577	PMID:18849486	PCS		1/1			C	HPO:probinson[2022-06-08]
OMIM:613112	Macrothrombocytopenia, autosomal dominant, tubb1-related		HP:0003540	PMID:18849486	PCS		0/2			P	HPO:skoehler[2014-11-27];HPO:probinson[2022-06-08]
OMIM:613112	Macrothrombocytopenia, autosomal dominant, tubb1-related		HP:0040185	PMID:18849486	PCS		2/2			P	HPO:skoehler[2015-12-30];HPO:probinson[2022-06-08]
OMIM:613112	Macrothrombocytopenia, autosomal dominant, tubb1-related		HP:0000006	PMID:18849486	PCS					I	HPO:skoehler[2010-06-19];HPO:probinson[2022-06-08]
OMIM:106750	Anonychia with flexural pigmentation		HP:0000958	OMIM:106750	TAS					P	HPO:skoehler[2009-02-17]
OMIM:106750	Anonychia with flexural pigmentation		HP:0007471	OMIM:106750	IEA					P	HPO:iea[2009-02-17]
OMIM:106750	Anonychia with flexural pigmentation		HP:0000006	OMIM:106750	IEA					I	HPO:iea[2009-02-17]
OMIM:106750	Anonychia with flexural pigmentation		HP:0001798	OMIM:106750	IEA					P	HPO:iea[2009-02-17]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003236	PMID:17444505	PCS		HP:0040283			P	HPO:skoehler[2013-08-13];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0030059	OMIM:611705	IEA					P	HPO:skoehler[2018-10-08]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003198	PMID:17444505	PCS		5/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003551	PMID:17444505	PCS		5/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0011717	PMID:17444505	PCS		1/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003593	OMIM:611705	TAS		3/5			C	HPO:skoehler[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0001270	PMID:17444505	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0011675	PMID:17444505	PCS		4/4			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0030319	PMID:17444505	PCS		5/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0012666	PMID:17444505	PCS		4/4			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0100297	PMID:17444505	PCS		2/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0009046	PMID:17444505	PCS		5/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003789	PMID:17444505	PCS		3/5			P	HPO:probinson[2023-03-12];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0001645	PMID:17444505	PCS		4/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003623	PMID:17444505	PCS		2/5			C	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0001644	PMID:17444505	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003324	PMID:17444505	PCS		5/5			P	HPO:skoehler[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003687	PMID:17444505	PCS		5/5			P	HPO:skoehler[2010-06-20];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0002650	PMID:17444505	PCS		1/5			P	HPO:skoehler[2017-07-13];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0034392	PMID:17444505	PCS		5/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0008981	PMID:17444505	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0000508	PMID:17444505	PCS		5/5			P	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0000007	PMID:17444505	PCS					I	HPO:iea[2009-02-17];HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0001635	PMID:17444505	PCS		1/4			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0001678	PMID:17444505	PCS		1/5			P	HPO:probinson[2023-03-12]
OMIM:611705	Congenital myopathy 5 with cardiomyopathy		HP:0003557	PMID:17444505	PCS		5/5			P	HPO:probinson[2023-03-12];HPO:probinson[2023-03-12]
ORPHA:79414	Woolly hair nevus		HP:0002212	ORPHA:79414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0002213	ORPHA:79414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0011365	ORPHA:79414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0040149	ORPHA:79414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0007534	ORPHA:79414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0034275	ORPHA:79414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0001100	ORPHA:79414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0001156	ORPHA:79414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0006304	ORPHA:79414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0009917	ORPHA:79414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0011387	ORPHA:79414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79414	Woolly hair nevus		HP:0000826	ORPHA:79414	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001387	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001824	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001945	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002039	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002315	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002633	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002637	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0005216	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0011227	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0012378	ORPHA:397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000505	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000597	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000716	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001369	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001596	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001903	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0003565	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0005413	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0005764	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0011899	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0030164	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0030783	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0033123	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0033834	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:6000502	ORPHA:397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000083	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000206	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000365	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000405	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000421	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000508	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000572	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000639	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000648	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000651	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000790	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000873	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0000975	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001123	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001251	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001260	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001287	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001324	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001399	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001645	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001701	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0001872	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002027	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002103	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002321	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002367	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002647	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0002829	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0003326	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0003401	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0004420	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0005112	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0005244	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0009830	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0011658	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0011675	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0012735	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0031246	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0100576	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0100721	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0100758	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0100776	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0100809	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397	Giant cell arteritis		HP:0200042	ORPHA:397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000028	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000035	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000045	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000048	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000051	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000054	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000062	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000137	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0001053	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0008665	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0008723	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0010459	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0010970	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0010987	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0012145	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0012861	ORPHA:199310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome		HP:0000954	ORPHA:199310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199310	Tetragametic chimerism syndrome	NOT	HP:0001263	ORPHA:199310	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001268	ORPHA:399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001347	ORPHA:399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002072	ORPHA:399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000496	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000713	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000716	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000718	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000722	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000734	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000737	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000738	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000739	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000741	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0000746	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001250	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001288	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001332	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001336	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001824	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002067	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002141	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002312	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002354	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001288	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002375	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0003324	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0004305	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0004408	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0007010	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0009088	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0025401	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0031473	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0031843	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0031845	ORPHA:399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0001262	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002059	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002063	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002169	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002300	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002340	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002500	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002540	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0002591	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0003107	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0003487	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0010794	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0030842	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0030955	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0031589	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0040140	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0045082	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0100785	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399	Huntington disease		HP:0200136	ORPHA:399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000678	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000939	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001083	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001166	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001249	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001519	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002160	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002757	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0004337	ORPHA:394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000545	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000646	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000767	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000768	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000822	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001387	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001761	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002204	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002209	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002637	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002650	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002808	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002857	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0004420	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0004936	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0100026	ORPHA:394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000218	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000486	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000501	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000518	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000541	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000648	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000708	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000709	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000716	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000729	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0000739	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001010	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001025	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001132	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001250	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001300	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001328	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001332	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001733	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0001933	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002039	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002040	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002071	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002170	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002239	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002240	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002353	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002500	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0002910	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0004374	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0007703	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0008770	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0012758	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0025300	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0033505	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0033724	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:394	Homocystinuria due to cystathionine beta-synthase deficiency		HP:0100790	ORPHA:394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:393	46,XX testicular difference of sex development		HP:0000026	ORPHA:393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:393	46,XX testicular difference of sex development		HP:0000062	ORPHA:393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:393	46,XX testicular difference of sex development		HP:0000147	ORPHA:393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:393	46,XX testicular difference of sex development		HP:0008734	ORPHA:393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0100247	ORPHA:396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0000716	ORPHA:396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0000775	ORPHA:396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0001824	ORPHA:396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0001944	ORPHA:396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0002360	ORPHA:396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0004395	ORPHA:396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:396	Chronic hiccup		HP:0100738	ORPHA:396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000708	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001288	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002011	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002061	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002156	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002160	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002493	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0003286	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0007340	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0012379	ORPHA:395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000725	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001250	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001251	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001268	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002313	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002518	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0003658	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0009830	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0410263	ORPHA:395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000709	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001249	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001254	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001263	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001269	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001328	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001345	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001508	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001727	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001977	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002069	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002104	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002315	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002500	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002625	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0006827	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0007359	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0008872	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0008935	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0012444	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0100543	ORPHA:395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000238	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000252	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000478	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000639	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0000648	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001297	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0001298	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002119	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002121	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:395	Homocystinuria due to methylene tetrahydrofolate reductase deficiency		HP:0002123	ORPHA:395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0000889	ORPHA:392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001171	ORPHA:392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001387	ORPHA:392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0030680	ORPHA:392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001199	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001629	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001631	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001678	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0002650	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0002808	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0004757	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0005916	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0006501	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0009777	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0011705	ORPHA:392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0000767	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0000772	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0000912	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001643	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0001679	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0002974	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0031095	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0004383	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0006101	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0006695	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0009829	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0010772	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0011304	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:392	Holt-Oram syndrome		HP:0200021	ORPHA:392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0001249	ORPHA:199318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0001263	ORPHA:199318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000252	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000256	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000286	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000400	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000411	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000486	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000494	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000717	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0000995	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0001250	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0001252	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0002007	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0004209	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0004322	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0005274	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0007018	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0007302	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0030680	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199318	15q13.3 microdeletion syndrome		HP:0100753	ORPHA:199318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002665	ORPHA:391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002716	ORPHA:391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0005374	ORPHA:391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0012378	ORPHA:391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0000975	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0000989	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001824	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001945	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002039	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0003418	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0004396	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0011227	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0012735	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0030166	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0100749	ORPHA:391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0000988	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001251	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001744	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001880	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001888	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001903	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0001974	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002076	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002093	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002105	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002240	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002653	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002664	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0002797	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0005528	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0009830	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391	Classic Hodgkin lymphoma		HP:0025435	ORPHA:391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000219	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000307	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000331	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000592	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0001518	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0002007	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0002714	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0002750	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0004209	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0004322	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0004482	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0008897	ORPHA:231137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000066	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000322	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000324	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000325	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000460	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000527	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000582	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0000975	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0001212	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0001786	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0001943	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0002213	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0006889	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0008872	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0009890	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0011342	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231137	Silver-Russell syndrome due to 7p11.2p13 microduplication		HP:0011471	ORPHA:231137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0002164	ORPHA:1401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0002212	ORPHA:1401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0009755	ORPHA:1401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0000072	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0000175	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0000190	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0000316	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0000958	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0000966	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0001251	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0002710	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0005280	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0006349	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0010297	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0030011	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0100750	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0200160	ORPHA:1401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome		HP:0004704	ORPHA:1401	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome	NOT	HP:0001270	ORPHA:1401	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1401	CHAND syndrome	NOT	HP:0200041	ORPHA:1401	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0002304	ORPHA:240094	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0031825	ORPHA:240094	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0002317	ORPHA:240094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0001621	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0002141	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0002464	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0005329	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0031434	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0031814	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0031908	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0031937	ORPHA:240094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0000726	ORPHA:240094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0002505	ORPHA:240094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0002527	ORPHA:240094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0007311	ORPHA:240094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0009053	ORPHA:240094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0000571	ORPHA:240094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0000643	ORPHA:240094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome		HP:0000657	ORPHA:240094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome	NOT	HP:0002063	ORPHA:240094	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:240094	Progressive supranuclear palsy-pure akinesia with gait freezing syndrome	NOT	HP:0002067	ORPHA:240094	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0000175	ORPHA:2736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0001539	ORPHA:2736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0000136	ORPHA:2736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0000185	ORPHA:2736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0000193	ORPHA:2736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0000238	ORPHA:2736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0000278	ORPHA:2736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2736	Lethal omphalocele-cleft palate syndrome		HP:0100333	ORPHA:2736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0000160	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0000233	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0000316	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0000347	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0001156	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0001171	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0001231	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0006101	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0008388	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0009804	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0100335	ORPHA:1406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0000322	ORPHA:1406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0000431	ORPHA:1406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0005916	ORPHA:1406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0000400	ORPHA:1406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1406	Charlie M syndrome		HP:0001199	ORPHA:1406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2730	Postaxial tetramelic oligodactyly		HP:0001167	ORPHA:2730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2730	Postaxial tetramelic oligodactyly		HP:0005916	ORPHA:2730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2730	Postaxial tetramelic oligodactyly		HP:0012165	ORPHA:2730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2730	Postaxial tetramelic oligodactyly		HP:0100257	ORPHA:2730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0000365	ORPHA:2732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0000486	ORPHA:2732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0000567	ORPHA:2732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0000639	ORPHA:2732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0000648	ORPHA:2732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0001250	ORPHA:2732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0001251	ORPHA:2732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0001276	ORPHA:2732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0001347	ORPHA:2732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0002119	ORPHA:2732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0002120	ORPHA:2732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0002167	ORPHA:2732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0002353	ORPHA:2732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2732	Olivopontocerebellar atrophy-deafness syndrome		HP:0002542	ORPHA:2732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0002017	ORPHA:79403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0003270	ORPHA:79403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0004399	ORPHA:79403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0008066	ORPHA:79403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0011100	ORPHA:79403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0200097	ORPHA:79403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0000070	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0000075	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0000110	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0000126	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0000790	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0001561	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0001581	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0006297	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0010477	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0012227	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0100577	ORPHA:79403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0000656	ORPHA:79403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0001057	ORPHA:79403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0001059	ORPHA:79403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79403	Junctional epidermolysis bullosa with pyloric atresia		HP:0008404	ORPHA:79403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0000389	ORPHA:199302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0100335	ORPHA:199302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0000220	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0000708	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0001518	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0001572	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0006332	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0009088	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0011438	ORPHA:199302	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0031469	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0040115	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0100336	ORPHA:199302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0000405	ORPHA:199302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0000668	ORPHA:199302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0001328	ORPHA:199302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0001537	ORPHA:199302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0001561	ORPHA:199302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0001696	ORPHA:199302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199302	Isolated cleft lip		HP:0001762	ORPHA:199302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002064	ORPHA:99013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0000012	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0000605	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0000639	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0000648	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0001272	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0001611	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002166	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002395	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0003200	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0003474	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0003487	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0006895	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0007018	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0007164	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0007256	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0007340	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0008322	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0011446	ORPHA:99013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0000543	ORPHA:99013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0001260	ORPHA:99013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0001761	ORPHA:99013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002120	ORPHA:99013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002500	ORPHA:99013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002650	ORPHA:99013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0003484	ORPHA:99013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0001328	ORPHA:99013	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002015	ORPHA:99013	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0002354	ORPHA:99013	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99013	Spastic paraplegia type 7		HP:0012514	ORPHA:99013	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001030	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001508	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001510	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001581	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001597	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0006297	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0008066	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0011830	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0020117	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0200035	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0200041	ORPHA:79404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001211	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001609	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001798	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001818	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001903	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002094	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0004395	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0010307	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0031446	ORPHA:79404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000003	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000010	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000014	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000016	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000070	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000072	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000081	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000107	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000126	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000481	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000939	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000969	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001057	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001596	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001602	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001615	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001644	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001944	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001955	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002013	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002019	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002043	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002087	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002090	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002098	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002860	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002878	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0003111	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0004057	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0004386	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0006000	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0008404	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0008682	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0010476	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0012227	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0100518	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0100806	ORPHA:79404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0000999	ORPHA:79404	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001250	ORPHA:79404	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0001662	ORPHA:79404	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79404	Severe generalized junctional epidermolysis bullosa		HP:0002107	ORPHA:79404	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0012252	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0031464	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0000670	ORPHA:79405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0008066	ORPHA:79405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0011355	ORPHA:79405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0001030	ORPHA:79405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0001075	ORPHA:79405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0006297	ORPHA:79405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0008404	ORPHA:79405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0001056	ORPHA:79405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0001798	ORPHA:79405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0004386	ORPHA:79405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0020117	ORPHA:79405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa		HP:0200097	ORPHA:79405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0000079	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0000478	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0000982	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0001510	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0001903	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0001965	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0002671	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0002860	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0004057	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0010562	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79405	Junctional epidermolysis bullosa inversa	NOT	HP:0012056	ORPHA:79405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0000365	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0000648	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0000763	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001251	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001260	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001262	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001284	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001288	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001324	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001337	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0001761	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0002385	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0002463	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0002650	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0002808	ORPHA:99014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0003712	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0007328	ORPHA:99014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0009830	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99014	X-linked Charcot-Marie-Tooth disease type 5		HP:0040129	ORPHA:99014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0002653	ORPHA:389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0002797	ORPHA:389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0000964	ORPHA:389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0000988	ORPHA:389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001744	ORPHA:389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001945	ORPHA:389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0002240	ORPHA:389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0002716	ORPHA:389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0012735	ORPHA:389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0000155	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0000365	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0000873	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001251	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001260	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001268	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001510	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001824	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001873	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001882	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0002108	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0003073	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0003249	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0034323	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0034769	ORPHA:389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0001399	ORPHA:389	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0002093	ORPHA:389	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:389	Langerhans cell histiocytosis		HP:0030991	ORPHA:389	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0000253	ORPHA:477814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0034311	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0001250	ORPHA:477814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0001263	ORPHA:477814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0002187	ORPHA:477814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0100704	ORPHA:477814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0002719	ORPHA:477814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0004322	ORPHA:477814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0004325	ORPHA:477814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0000648	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0000823	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0001252	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0001531	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0002110	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0002665	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0003202	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0005387	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0011330	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0012191	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0012444	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0032218	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477814	Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome		HP:0033725	ORPHA:477814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0002014	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0004322	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0004387	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0031369	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0100806	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0002251	ORPHA:388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0005214	ORPHA:388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0012719	ORPHA:388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0001531	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0001824	ORPHA:388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0003270	ORPHA:388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0011968	ORPHA:388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0034754	ORPHA:388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:6000224	ORPHA:388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0001510	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0001561	ORPHA:388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0002017	ORPHA:388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0002019	ORPHA:388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:388	Hirschsprung disease		HP:0002027	ORPHA:388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0001030	ORPHA:79406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0001798	ORPHA:79406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0006297	ORPHA:79406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0007455	ORPHA:79406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0008066	ORPHA:79406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0008404	ORPHA:79406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0000670	ORPHA:79406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0000975	ORPHA:79406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0011355	ORPHA:79406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0020117	ORPHA:79406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa		HP:0200097	ORPHA:79406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0000079	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0000478	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0000982	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0001056	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0001075	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0001510	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0001903	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0001965	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0002671	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0002860	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0004057	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0004386	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0010562	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0012056	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0012252	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79406	Late-onset junctional epidermolysis bullosa	NOT	HP:0031464	ORPHA:79406	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0000639	ORPHA:99015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0000648	ORPHA:99015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0000763	ORPHA:99015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0001249	ORPHA:99015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0001251	ORPHA:99015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0001257	ORPHA:99015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0001260	ORPHA:99015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0001324	ORPHA:99015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0001347	ORPHA:99015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0001376	ORPHA:99015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0002064	ORPHA:99015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0002071	ORPHA:99015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0002204	ORPHA:99015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0002205	ORPHA:99015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0002607	ORPHA:99015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0003487	ORPHA:99015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99015	Spastic paraplegia type 2		HP:0005340	ORPHA:99015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0000325	ORPHA:231140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0000331	ORPHA:231140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001518	ORPHA:231140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0002750	ORPHA:231140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0004322	ORPHA:231140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0100555	ORPHA:231140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0000218	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0000411	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0000678	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0004209	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0004325	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0004482	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0008872	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0008897	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0011220	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0100559	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0100560	ORPHA:231140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0000811	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001052	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001249	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001250	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001270	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001540	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001943	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001998	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0010442	ORPHA:231140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0000975	ORPHA:231140	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231140	Silver-Russell syndrome due to an imprinting defect of 11p15		HP:0001476	ORPHA:231140	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0000325	ORPHA:231147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0001518	ORPHA:231147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0002007	ORPHA:231147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0004209	ORPHA:231147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0000175	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0000324	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0000924	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0000975	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0001263	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0001511	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0001622	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0001627	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0001943	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0002194	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0003241	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0005484	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0008872	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0030884	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0100555	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231147	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11		HP:0100559	ORPHA:231147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0001250	ORPHA:382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0000708	ORPHA:382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002071	ORPHA:382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002465	ORPHA:382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0007153	ORPHA:382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0010864	ORPHA:382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0011344	ORPHA:382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0100022	ORPHA:382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0000717	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0000718	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0000752	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0001251	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0001332	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002069	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002072	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002123	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002305	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002384	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0002457	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0010819	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0100716	ORPHA:382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:382	Guanidinoacetate methyltransferase deficiency		HP:0001252	ORPHA:382	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000750	ORPHA:477817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001263	ORPHA:477817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001999	ORPHA:477817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0008872	ORPHA:477817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0008947	ORPHA:477817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0031936	ORPHA:477817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000708	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001382	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001531	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001627	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001760	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0002360	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0002460	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0002936	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0003693	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0009027	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0012210	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0012450	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0200101	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0410263	ORPHA:477817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000219	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000319	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000325	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000343	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000377	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000445	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000486	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000494	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000762	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0000763	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001629	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001631	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001647	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001655	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001719	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001762	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001763	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0001852	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0002136	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0002623	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0003380	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0003396	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0004691	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0004942	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0005301	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477817	PMP22-RAI1 contiguous gene duplication syndrome		HP:0008081	ORPHA:477817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000670	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001030	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001056	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001075	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001371	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001510	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001903	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0004057	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0004386	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0008066	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0012532	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0200097	ORPHA:79408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000478	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000716	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000739	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001798	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001891	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001965	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0002860	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0008404	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0011354	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0031446	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0032676	ORPHA:79408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000083	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000099	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000160	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000572	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000794	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000823	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000938	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000939	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001057	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001581	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001644	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0001917	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0002015	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0002020	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0002839	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0004395	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0004791	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0008366	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0010296	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0011936	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0012056	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0012227	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0012390	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0012622	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0031831	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0031903	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0100508	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0100512	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0200020	ORPHA:79408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0000079	ORPHA:79408	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form		HP:0031464	ORPHA:79408	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form	NOT	HP:0000982	ORPHA:79408	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form	NOT	HP:0002671	ORPHA:79408	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form	NOT	HP:0006297	ORPHA:79408	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79408	Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form	NOT	HP:0012252	ORPHA:79408	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0001030	ORPHA:79409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0000079	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0000670	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0001056	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0001075	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0001798	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0004386	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0008066	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0008404	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0011355	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0031464	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0200097	ORPHA:79409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0000402	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0001510	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0001903	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0002043	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0004057	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0007446	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0012227	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa		HP:0025416	ORPHA:79409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0000478	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0000982	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0001965	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0002671	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0002860	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0006297	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0012056	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79409	Recessive dystrophic epidermolysis bullosa inversa	NOT	HP:0012252	ORPHA:79409	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:384	Huriez syndrome		HP:0000958	ORPHA:384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:384	Huriez syndrome		HP:0000982	ORPHA:384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:384	Huriez syndrome		HP:0001597	ORPHA:384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:384	Huriez syndrome		HP:0001792	ORPHA:384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:384	Huriez syndrome		HP:0008065	ORPHA:384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:384	Huriez syndrome		HP:0011838	ORPHA:384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:384	Huriez syndrome		HP:0100679	ORPHA:384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0000325	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001508	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001511	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001518	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001562	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0002750	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0004209	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0004322	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0008897	ORPHA:231144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0000324	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001270	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001328	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001537	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0001558	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0004482	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0008846	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0008947	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0011220	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231144	Silver-Russell syndrome due to 11p15 microduplication		HP:0011800	ORPHA:231144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000023	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000028	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000071	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000079	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000160	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000174	ORPHA:2719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000252	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000268	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000407	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000463	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000478	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000504	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000518	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000545	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000639	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000656	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000691	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0000963	ORPHA:2719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001107	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001139	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001166	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001172	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001249	ORPHA:2719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001251	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001257	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001305	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001347	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001376	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001510	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001608	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0001903	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0002071	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0002305	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0002353	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0002510	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0003196	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0004322	ORPHA:2719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0005280	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0005561	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0005599	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0007256	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0007730	ORPHA:2719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0007957	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0008056	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2719	Oculocerebral hypopigmentation syndrome, Cross type		HP:0100022	ORPHA:2719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0000238	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0000499	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0000534	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0000639	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0000952	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001053	ORPHA:381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001249	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001250	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001251	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001252	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001257	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001263	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001315	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001541	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001744	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001873	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001874	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001882	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0001945	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0002021	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0002084	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0002216	ORPHA:381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0002218	ORPHA:381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0002240	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0002716	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0002721	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0003119	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0004313	ORPHA:381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0004322	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0005528	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0006824	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0007730	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0010741	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0011364	ORPHA:381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0012115	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:381	Griscelli syndrome		HP:0100022	ORPHA:381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0000238	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0000256	ORPHA:380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0000316	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0000348	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0000431	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0000506	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0000776	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001162	ORPHA:380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001177	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001250	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001256	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001274	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001363	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001537	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001770	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001830	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0001841	ORPHA:380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0002007	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0005616	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0006101	ORPHA:380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0010059	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:380	Greig cephalopolysyndactyly syndrome		HP:0011304	ORPHA:380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0006292	ORPHA:199306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000175	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000202	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000220	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000403	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000750	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0002033	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0008872	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0009088	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0100334	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0200136	ORPHA:199306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000405	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000689	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0001611	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0004395	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0006342	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0010294	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0011044	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0100337	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0200153	ORPHA:199306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199306	Cleft lip/palate		HP:0000327	ORPHA:199306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0000691	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0000692	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0000982	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0001231	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0001596	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0001800	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0002231	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0006482	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0008070	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0009804	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2722	Odonto-onycho dysplasia-alopecia syndrome		HP:0045075	ORPHA:2722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000112	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000657	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001249	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001251	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001252	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001263	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001320	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002104	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002419	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002793	ORPHA:220497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000276	ORPHA:220497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000358	ORPHA:220497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000639	ORPHA:220497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001288	ORPHA:220497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0004422	ORPHA:220497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0011968	ORPHA:220497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000083	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000175	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000202	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000238	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000426	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000463	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000486	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000508	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000612	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0000864	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001161	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001250	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001274	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0001337	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002084	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002126	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002251	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002553	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0002650	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220497	Joubert syndrome with renal defect		HP:0030680	ORPHA:220497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2724	Odontomatosis-aortae esophagus stenosis syndrome		HP:0001399	ORPHA:2724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2724	Odontomatosis-aortae esophagus stenosis syndrome		HP:0002015	ORPHA:2724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2724	Odontomatosis-aortae esophagus stenosis syndrome		HP:0002621	ORPHA:2724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2724	Odontomatosis-aortae esophagus stenosis syndrome		HP:0011068	ORPHA:2724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2724	Odontomatosis-aortae esophagus stenosis syndrome		HP:0012819	ORPHA:2724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2724	Odontomatosis-aortae esophagus stenosis syndrome		HP:0030680	ORPHA:2724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002067	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0006921	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002063	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0001337	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0000496	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0001268	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002527	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002172	ORPHA:240085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002098	ORPHA:240085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002068	ORPHA:240085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0001332	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002548	ORPHA:240085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0000741	ORPHA:240085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0000716	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0010794	ORPHA:240085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0000511	ORPHA:240085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0000570	ORPHA:240085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002167	ORPHA:240085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome	NOT	HP:0000739	ORPHA:240085	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:240085	Progressive supranuclear palsy-predominant parkinsonism syndrome		HP:0002354	ORPHA:240085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000556	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000657	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001249	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001251	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001252	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001263	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001320	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002104	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002419	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002793	ORPHA:220493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000276	ORPHA:220493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000639	ORPHA:220493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001288	ORPHA:220493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0004422	ORPHA:220493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0011968	ORPHA:220493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000175	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000202	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000238	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000358	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000426	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000463	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000480	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000486	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000508	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000572	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000612	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0000864	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001161	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001250	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001274	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001337	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001651	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0001829	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002084	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002126	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002251	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002553	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0002650	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0003468	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220493	Joubert syndrome with ocular defect		HP:0030680	ORPHA:220493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000028	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000046	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000093	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000252	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000356	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000365	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000403	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000508	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000568	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000581	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000646	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000685	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000687	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000691	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000750	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0001018	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0001256	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0001270	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0001511	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0008551	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0008897	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0030148	ORPHA:2728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0000175	ORPHA:2728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0001631	ORPHA:2728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0012619	ORPHA:2728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2728	Blepharophimosis-intellectual disability syndrome, Ohdo type		HP:0012768	ORPHA:2728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0008066	ORPHA:79410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0011355	ORPHA:79410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0012221	ORPHA:79410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0000987	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0000989	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0001030	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0001056	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0001075	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0001231	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0001798	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0007446	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0008388	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0008404	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0010562	ORPHA:79410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0000478	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0000670	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0001792	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0004057	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0030350	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0045059	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0200037	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0200041	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form		HP:0200097	ORPHA:79410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0000079	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0000982	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0001510	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0001903	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0001965	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0002671	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0002860	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0004386	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0006297	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0012056	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0012252	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79410	Localized dystrophic epidermolysis bullosa, pretibial form	NOT	HP:0031464	ORPHA:79410	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0000230	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0000246	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0000388	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0000964	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0000992	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0001034	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0001287	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0001744	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0001874	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0001945	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0002021	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0002024	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0002205	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0002240	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0002575	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0006510	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0012733	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0100523	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0100533	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0100721	ORPHA:379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0100806	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:379	Chronic granulomatous disease		HP:0200042	ORPHA:379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0011354	ORPHA:79411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0001030	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0001056	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0001075	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0001798	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0008066	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0008404	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0009723	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0200097	ORPHA:79411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0000670	ORPHA:79411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0001057	ORPHA:79411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0200041	ORPHA:79411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa		HP:0001000	ORPHA:79411	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0000079	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0000478	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0000982	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0001510	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0001903	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0001965	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0002671	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0002860	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0004057	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0004386	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0006297	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0012056	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0012252	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79411	Self-improving dystrophic epidermolysis bullosa	NOT	HP:0031464	ORPHA:79411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0000091	ORPHA:2720	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0000218	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0000238	ORPHA:2720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0000365	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0000518	ORPHA:2720	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0000613	ORPHA:2720	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0000639	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001107	ORPHA:2720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001166	ORPHA:2720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001249	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001250	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001251	ORPHA:2720	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001263	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001276	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001874	ORPHA:2720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0001931	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0002363	ORPHA:2720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0003272	ORPHA:2720	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0004322	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0004349	ORPHA:2720	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0007360	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0007513	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0007730	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0010662	ORPHA:2720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0010978	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2720	Oculocerebral hypopigmentation syndrome, Preus type		HP:0011364	ORPHA:2720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0011789	ORPHA:90673	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0000851	ORPHA:90673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0002925	ORPHA:90673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0006579	ORPHA:90673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0025484	ORPHA:90673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0031219	ORPHA:90673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0031507	ORPHA:90673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0000158	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0001254	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0001265	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0001537	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0001662	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0002019	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0003265	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0004491	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0005930	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0005990	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0008223	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0008828	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0008872	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0025429	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0031220	ORPHA:90673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0000969	ORPHA:90673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0001252	ORPHA:90673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations		HP:0002045	ORPHA:90673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations	NOT	HP:0000853	ORPHA:90673	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations	NOT	HP:0011437	ORPHA:90673	TAS					H	ORPHA:orphadata[2025-10-22]
ORPHA:90673	Hypothyroidism due to TSH receptor mutations	NOT	HP:0030057	ORPHA:90673	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0005990	ORPHA:90674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0008245	ORPHA:90674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0025483	ORPHA:90674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0031098	ORPHA:90674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0031208	ORPHA:90674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0031219	ORPHA:90674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0031507	ORPHA:90674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000053	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000158	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000270	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000282	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000870	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000958	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001265	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001508	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001510	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001537	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001609	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001615	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0002019	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0002045	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0002690	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0002750	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0003124	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0003265	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0004491	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0005280	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0005930	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0006579	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0008828	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0008872	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0012378	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0012758	ORPHA:90674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001252	ORPHA:90674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001254	ORPHA:90674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0001662	ORPHA:90674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0002312	ORPHA:90674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0007018	ORPHA:90674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000716	ORPHA:90674	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency		HP:0000853	ORPHA:90674	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency	NOT	HP:0011437	ORPHA:90674	TAS					H	ORPHA:orphadata[2025-10-22]
ORPHA:90674	Isolated thyroid-stimulating hormone deficiency	NOT	HP:0030057	ORPHA:90674	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0000750	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001252	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001508	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001649	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001824	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001873	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001876	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001892	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0002013	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0100502	ORPHA:35858	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0200118	ORPHA:35858	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0410216	ORPHA:35858	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001889	ORPHA:35858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001972	ORPHA:35858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0004821	ORPHA:35858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0000093	ORPHA:35858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0000980	ORPHA:35858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001875	ORPHA:35858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0001923	ORPHA:35858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0004823	ORPHA:35858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0020061	ORPHA:35858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0032566	ORPHA:35858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0000206	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0000707	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0002019	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0002376	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0004396	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0030318	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0031936	ORPHA:35858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35858	Imerslund-Gräsbeck syndrome		HP:0002721	ORPHA:35858	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0010797	ORPHA:252054	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0002017	ORPHA:252054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0002315	ORPHA:252054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0002321	ORPHA:252054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0006880	ORPHA:252054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0009711	ORPHA:252054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0010576	ORPHA:252054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0030915	ORPHA:252054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0000011	ORPHA:252054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0003484	ORPHA:252054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0007340	ORPHA:252054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0009713	ORPHA:252054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0012534	ORPHA:252054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0030144	ORPHA:252054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0100661	ORPHA:252054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252054	Hemangioblastoma		HP:0000238	ORPHA:252054	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0000478	ORPHA:99000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0000504	ORPHA:99000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0000505	ORPHA:99000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0000551	ORPHA:99000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0001123	ORPHA:99000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0001139	ORPHA:99000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0007677	ORPHA:99000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0007730	ORPHA:99000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99000	Adult-onset foveomacular vitelliform dystrophy		HP:0007899	ORPHA:99000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0000790	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0000967	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0001698	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0001701	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0001873	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0001903	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0002094	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0002829	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0003138	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0003236	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0003326	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0003493	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0003565	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0005184	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0005421	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0011227	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0025300	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0025343	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0030057	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0045042	ORPHA:231111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0001945	ORPHA:231111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0045073	ORPHA:231111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231111	Drug-induced lupus erythematosus		HP:0025142	ORPHA:231111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357154	Oral submucous fibrosis		HP:0000160	ORPHA:357154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357154	Oral submucous fibrosis		HP:0000163	ORPHA:357154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357154	Oral submucous fibrosis		HP:0000211	ORPHA:357154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357154	Oral submucous fibrosis		HP:0000600	ORPHA:357154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357154	Oral submucous fibrosis		HP:0001371	ORPHA:357154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357154	Oral submucous fibrosis		HP:0012182	ORPHA:357154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357154	Oral submucous fibrosis		HP:0100825	ORPHA:357154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0000169	ORPHA:2709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0000212	ORPHA:2709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0000684	ORPHA:2709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0001131	ORPHA:2709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0000505	ORPHA:2709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0005216	ORPHA:2709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0006482	ORPHA:2709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2709	Oculodental syndrome, Rutherfurd type		HP:0007957	ORPHA:2709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002172	ORPHA:240071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002527	ORPHA:240071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000514	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0001268	ORPHA:240071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0030953	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000633	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000622	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000643	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000613	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0007086	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0100710	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0007164	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000605	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002068	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0001300	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0006921	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002067	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002141	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000511	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002530	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002304	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0001337	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0001260	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0007158	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0001332	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0000570	ORPHA:240071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0007256	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240071	Classic progressive supranuclear palsy syndrome		HP:0002548	ORPHA:240071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0011123	ORPHA:542592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0025528	ORPHA:542592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0000819	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0001030	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0001075	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0002814	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0010783	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0011990	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0032217	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0032252	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0100585	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0200034	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0200035	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0200036	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0200042	ORPHA:542592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0000271	ORPHA:542592	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0001155	ORPHA:542592	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0001965	ORPHA:542592	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0002973	ORPHA:542592	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0000820	ORPHA:542592	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542592	Necrobiosis lipoidica		HP:0002860	ORPHA:542592	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000164	ORPHA:2712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000174	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000175	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000176	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000275	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000343	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000365	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000407	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000426	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000456	ORPHA:2712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000482	ORPHA:2712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000501	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000508	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000518	ORPHA:2712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000541	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000568	ORPHA:2712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000612	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000677	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000684	ORPHA:2712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0000692	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001083	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001169	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001249	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001263	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001634	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001643	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001671	ORPHA:2712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0001765	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0002553	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0002566	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0002650	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0002857	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0002967	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0002974	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0004209	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0004691	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0004969	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0006315	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0008872	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0009778	ORPHA:2712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0010327	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0010339	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2712	Oculofaciocardiodental syndrome		HP:0011090	ORPHA:2712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000568	ORPHA:2714	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0002099	ORPHA:2714	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000175	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000252	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000391	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000400	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000518	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000555	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0001249	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0001257	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0001263	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0001382	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0001511	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0001773	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0002705	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0004322	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0006913	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0007370	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0007968	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0008386	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0200055	ORPHA:2714	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000501	ORPHA:2714	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0000541	ORPHA:2714	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2714	Oculo-palato-cerebral syndrome		HP:0002283	ORPHA:2714	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000083	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000093	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000154	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000275	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000298	ORPHA:2715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000303	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000400	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000486	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000505	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000518	ORPHA:2715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0000648	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001053	ORPHA:2715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001252	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001257	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001264	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001266	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001347	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001852	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0002187	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0002650	ORPHA:2715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0004322	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0001382	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0007360	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0007703	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0008046	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0009748	ORPHA:2715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0010620	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0010669	ORPHA:2715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2715	Severe oculo-renal-cerebellar syndrome		HP:0100820	ORPHA:2715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0200063	ORPHA:220460	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0003003	ORPHA:220460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0004394	ORPHA:220460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0004783	ORPHA:220460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0005227	ORPHA:220460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0006753	ORPHA:220460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0030255	ORPHA:220460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0100896	ORPHA:220460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0000131	ORPHA:220460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0000854	ORPHA:220460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0005562	ORPHA:220460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0009592	ORPHA:220460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0010614	ORPHA:220460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0012740	ORPHA:220460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0040276	ORPHA:220460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0002672	ORPHA:220460	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0002894	ORPHA:220460	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0002895	ORPHA:220460	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0003002	ORPHA:220460	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0006744	ORPHA:220460	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0008256	ORPHA:220460	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis		HP:0030434	ORPHA:220460	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220460	Attenuated familial adenomatous polyposis	NOT	HP:0007649	ORPHA:220460	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0000316	ORPHA:2717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0000456	ORPHA:2717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0000528	ORPHA:2717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0000568	ORPHA:2717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0000579	ORPHA:2717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0000636	ORPHA:2717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0001126	ORPHA:2717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0001545	ORPHA:2717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0002025	ORPHA:2717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2717	Oculotrichoanal syndrome		HP:0010720	ORPHA:2717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0000764	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0002495	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0002936	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0003202	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0003447	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0007141	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0007249	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0007267	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0007328	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0008959	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0008994	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0008997	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0009053	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0010830	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0011096	ORPHA:101097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0000925	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001171	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001284	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001315	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001371	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001604	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001609	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001761	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001762	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0002317	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0002359	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0002505	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0003731	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0006858	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0007233	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0008954	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0011727	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0030237	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0031629	ORPHA:101097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0000765	ORPHA:101097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness		HP:0001270	ORPHA:101097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101097	Autosomal recessive Charcot-Marie-Tooth disease with hoarseness	NOT	HP:0000762	ORPHA:101097	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0000989	ORPHA:79400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0003341	ORPHA:79400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0007446	ORPHA:79400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0007497	ORPHA:79400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0007585	ORPHA:79400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0008066	ORPHA:79400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0025238	ORPHA:79400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0002046	ORPHA:79400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0003401	ORPHA:79400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0003489	ORPHA:79400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0012513	ORPHA:79400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0200035	ORPHA:79400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0000975	ORPHA:79400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0007556	ORPHA:79400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0010765	ORPHA:79400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0031446	ORPHA:79400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0200041	ORPHA:79400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0001056	ORPHA:79400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0001075	ORPHA:79400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0008404	ORPHA:79400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0030350	ORPHA:79400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex		HP:0200097	ORPHA:79400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79400	Localized epidermolysis bullosa simplex	NOT	HP:0009123	ORPHA:79400	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0000982	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0001030	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0001034	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0007446	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0008066	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0020073	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0031045	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0200041	ORPHA:79401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement		HP:0000164	ORPHA:79401	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement	NOT	HP:0000478	ORPHA:79401	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement	NOT	HP:0001627	ORPHA:79401	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79401	PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement	NOT	HP:0002012	ORPHA:79401	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000175	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000366	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000430	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000446	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000463	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000482	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000598	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000670	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000682	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001770	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0004209	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0006101	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0006323	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0009804	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0010761	ORPHA:2710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000011	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000161	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000187	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000303	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000316	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000348	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000405	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000478	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000501	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000504	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000505	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000518	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000545	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000601	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000648	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000944	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001231	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001250	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001251	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001257	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001260	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001288	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001324	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001347	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001597	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0002212	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0002217	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0002313	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0002514	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0003103	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0003196	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0004437	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0007360	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0008070	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0008499	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000377	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0009843	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0011342	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0030084	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0100490	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0100774	ORPHA:2710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000286	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000347	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000365	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000486	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000490	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000525	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000582	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000639	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000679	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000889	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000940	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0000982	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001156	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001161	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001177	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001249	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001537	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001629	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0001943	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0002213	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0002299	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0003067	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0003312	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0010109	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0011675	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0030680	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2710	Oculodentodigital dysplasia		HP:0100335	ORPHA:2710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0000982	ORPHA:79402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0001000	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0001056	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0001057	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0001075	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0001510	ORPHA:79402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0001798	ORPHA:79402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0001903	ORPHA:79402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0002231	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0004552	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0006297	ORPHA:79402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0008066	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0008404	ORPHA:79402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79402	Intermediate generalized junctional epidermolysis bullosa		HP:0200097	ORPHA:79402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000938	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000939	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001007	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001369	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001495	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001999	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0002797	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0003040	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0005922	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0006234	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0009139	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0045039	ORPHA:371428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000248	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000916	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001230	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001482	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001626	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0003312	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0005441	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0011355	ORPHA:371428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000147	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000315	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000612	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0000822	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001059	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001085	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001249	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001539	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001629	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001631	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001634	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001647	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001678	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001680	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0001719	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0002659	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0005994	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0010314	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371428	Multicentric osteolysis-nodulosis-arthropathy spectrum		HP:0100651	ORPHA:371428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0003324	ORPHA:34516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0001260	ORPHA:34516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0002015	ORPHA:34516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0003551	ORPHA:34516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0003557	ORPHA:34516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0002505	ORPHA:34516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0003715	ORPHA:34516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0003805	ORPHA:34516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0012548	ORPHA:34516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0030951	ORPHA:34516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0004303	ORPHA:34516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:34516	DNAJB6-related limb-girdle muscular dystrophy D1		HP:0010548	ORPHA:34516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0002615	ORPHA:97292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0003115	ORPHA:97292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0005162	ORPHA:97292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0009805	ORPHA:97292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0000961	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0000969	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001635	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001658	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001695	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0002094	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0004372	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0006670	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0011675	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0012418	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0012764	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0030830	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0030848	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0030851	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0030876	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0100520	ORPHA:97292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001289	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001653	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001942	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0002151	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0002240	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0002321	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0003259	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0012251	ORPHA:97292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001259	ORPHA:97292	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97292	Cardiogenic shock		HP:0001708	ORPHA:97292	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001052	ORPHA:97297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0012758	ORPHA:97297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000243	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000252	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000293	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000297	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000520	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000589	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000648	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000664	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000998	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001105	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001274	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001376	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001511	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001525	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001662	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002013	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002079	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002104	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002187	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002205	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002360	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002540	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002719	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002803	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002870	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0003049	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0004322	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0005487	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0006471	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0006863	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0006895	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0008872	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0008936	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0010733	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0010864	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0012537	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0040082	ORPHA:97297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000016	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000175	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000278	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000316	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000347	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000358	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000431	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000463	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0000767	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001250	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001305	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001373	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002119	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0005280	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0006070	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0010291	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0011003	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0012448	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0012453	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0410030	ORPHA:97297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001081	ORPHA:97297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001640	ORPHA:97297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001671	ORPHA:97297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0001734	ORPHA:97297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002667	ORPHA:97297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97297	Bohring-Opitz syndrome		HP:0002885	ORPHA:97297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0003236	ORPHA:34515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0003560	ORPHA:34515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0003701	ORPHA:34515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0030099	ORPHA:34515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0001290	ORPHA:34515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0002515	ORPHA:34515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0003547	ORPHA:34515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0003749	ORPHA:34515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0005109	ORPHA:34515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0008981	ORPHA:34515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0001270	ORPHA:34515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0001644	ORPHA:34515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0002359	ORPHA:34515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0002650	ORPHA:34515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0003551	ORPHA:34515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0009046	ORPHA:34515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34515	FKRP-related limb-girdle muscular dystrophy R9		HP:0030092	ORPHA:34515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0000853	ORPHA:97290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0002730	ORPHA:97290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0002733	ORPHA:97290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0002757	ORPHA:97290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0002895	ORPHA:97290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0003002	ORPHA:97290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0003003	ORPHA:97290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0005994	ORPHA:97290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0006528	ORPHA:97290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0006735	ORPHA:97290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0006766	ORPHA:97290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0011798	ORPHA:97290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:0012288	ORPHA:97290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97290	Familial papillary thyroid carcinoma with renal papillary neoplasia		HP:3000037	ORPHA:97290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001249	ORPHA:438213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001344	ORPHA:438213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002136	ORPHA:438213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0008947	ORPHA:438213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0010862	ORPHA:438213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0012758	ORPHA:438213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000478	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000504	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000549	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000977	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001250	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001262	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001270	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001332	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002019	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002045	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002104	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002267	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002307	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002540	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002791	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002870	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0005957	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0010536	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0010863	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0011968	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0012171	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0100247	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0100512	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0100660	ORPHA:438213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000119	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000278	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000293	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000486	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000540	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000565	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000639	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000818	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000924	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000939	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001336	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001385	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001382	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001627	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002002	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002015	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002020	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002058	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002079	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0002650	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0004305	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0004322	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0007193	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0007655	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0007874	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0009890	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0010818	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0011097	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0011951	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0012448	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0012704	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0025313	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0030890	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0031622	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0100704	ORPHA:438213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000028	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000076	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000126	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000139	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000543	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000787	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000821	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000826	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000870	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0000938	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001331	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001629	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001631	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001642	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001643	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001647	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001655	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0001903	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0011747	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0031253	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438213	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome		HP:0040303	ORPHA:438213	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000327	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000343	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000518	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000541	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000545	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0002652	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0003196	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0004327	ORPHA:90653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000175	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000407	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000520	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000926	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0001634	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0002758	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0002829	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0001382	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0005930	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0100734	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:6000015	ORPHA:90653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0000572	ORPHA:90653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90653	Stickler syndrome type 1		HP:0001249	ORPHA:90653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000028	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000174	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000179	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000233	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000238	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000286	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000316	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000365	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000358	ORPHA:2701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000400	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000463	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000465	ORPHA:2701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000670	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0000767	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0001156	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0001231	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0001249	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0001639	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0001642	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0001800	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0002002	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0002162	ORPHA:2701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0002209	ORPHA:2701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0002750	ORPHA:2701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0003196	ORPHA:2701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0004322	ORPHA:2701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0005108	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0009811	ORPHA:2701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2701	Noonan syndrome-like disorder with loose anagen hair		HP:0100840	ORPHA:2701	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0000407	ORPHA:90654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0000518	ORPHA:90654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0000541	ORPHA:90654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0000545	ORPHA:90654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0004327	ORPHA:90654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0007957	ORPHA:90654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0000175	ORPHA:90654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:0000488	ORPHA:90654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90654	Stickler syndrome type 2		HP:6000015	ORPHA:90654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0001250	ORPHA:438216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0001263	ORPHA:438216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0002098	ORPHA:438216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0008872	ORPHA:438216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0002058	ORPHA:438216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0011344	ORPHA:438216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000218	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000219	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000252	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000276	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000286	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000293	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000297	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000324	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000348	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000430	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000431	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000455	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000463	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000506	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000545	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000582	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000637	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000736	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000739	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0001251	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0001332	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0002007	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0002136	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0002267	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0006481	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0006829	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0000377	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0010804	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0011081	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0011220	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0012899	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438216	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation		HP:0100660	ORPHA:438216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0001321	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0002120	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0002334	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0005306	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0010733	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0011427	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0012157	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0100308	ORPHA:2703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0000238	ORPHA:2703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2703	Port-wine nevi-mega cisterna magna-hydrocephalus syndrome		HP:0001250	ORPHA:2703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000010	ORPHA:2704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000020	ORPHA:2704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000028	ORPHA:2704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000076	ORPHA:2704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000083	ORPHA:2704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000126	ORPHA:2704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000796	ORPHA:2704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0000822	ORPHA:2704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0001959	ORPHA:2704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0002019	ORPHA:2704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2704	Urofacial syndrome		HP:0002607	ORPHA:2704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0000407	ORPHA:90658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0000762	ORPHA:90658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0001288	ORPHA:90658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0002936	ORPHA:90658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0007108	ORPHA:90658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0009053	ORPHA:90658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0000615	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0001288	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0001761	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0002166	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0002172	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0002522	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0002600	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0008944	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0008962	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0009027	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0009049	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0009130	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0010829	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0010830	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0010832	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0011727	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0012074	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0012391	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0030211	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0030237	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0031006	ORPHA:90658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0000360	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0001171	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0001263	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0001765	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0002141	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0002540	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0003376	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0008110	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0008124	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0009473	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0009916	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0011476	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90658	Charcot-Marie-Tooth disease type 1E		HP:0012735	ORPHA:90658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000248	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000252	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000278	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000347	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000582	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000587	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000648	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001166	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001249	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001263	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001328	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001833	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0002094	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0002098	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0002878	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0005469	ORPHA:2707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000154	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000159	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000177	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000233	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000275	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000276	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000286	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000319	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000322	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000384	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000482	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000486	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000506	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000545	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000581	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000639	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0000691	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001508	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001510	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0002223	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0002705	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0010547	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0011968	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0012745	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0045074	ORPHA:2707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001135	ORPHA:2707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0001139	ORPHA:2707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2707	Oculocerebrofacial syndrome, Kaufman type		HP:0008665	ORPHA:2707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0012232	ORPHA:51083	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0001662	ORPHA:51083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0001962	ORPHA:51083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0005110	ORPHA:51083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0001279	ORPHA:51083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0001645	ORPHA:51083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0001663	ORPHA:51083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0001678	ORPHA:51083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51083	Congenital short QT syndrome		HP:0004308	ORPHA:51083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0000762	ORPHA:101085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002460	ORPHA:101085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0003202	ORPHA:101085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0003474	ORPHA:101085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0007141	ORPHA:101085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0007220	ORPHA:101085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0011402	ORPHA:101085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0001155	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0001270	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0001284	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0001761	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002066	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002070	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002317	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002346	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002378	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002403	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002495	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0003376	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0003387	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0004463	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0007149	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0007327	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0007328	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0008944	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0009027	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0009053	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0009130	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0010831	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0010873	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0030237	ORPHA:101085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0000020	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0000407	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0000609	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0001252	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0001260	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002380	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002650	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0003394	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0003401	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0003691	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0008956	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0008994	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0008997	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0012452	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0012473	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0012785	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0030319	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0100543	ORPHA:101085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101085	Charcot-Marie-Tooth disease type 1F		HP:0002540	ORPHA:101085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0100521	ORPHA:97289	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0100634	ORPHA:97289	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0045026	ORPHA:97289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0100721	ORPHA:97289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0001824	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0002730	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0003118	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0003154	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0005345	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0007457	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0012735	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0030829	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0100568	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0100570	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0100749	ORPHA:97289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0000870	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0000938	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0002893	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0003072	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0004724	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0006767	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0008200	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0008261	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97289	Thymic neuroendocrine tumor		HP:0011761	ORPHA:97289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370103	Primary dystonia, DYT17 type		HP:0001260	ORPHA:370103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370103	Primary dystonia, DYT17 type		HP:0001618	ORPHA:370103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370103	Primary dystonia, DYT17 type		HP:0007325	ORPHA:370103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370103	Primary dystonia, DYT17 type		HP:0000473	ORPHA:370103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370103	Primary dystonia, DYT17 type		HP:0012179	ORPHA:370103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370103	Primary dystonia, DYT17 type	NOT	HP:0001300	ORPHA:370103	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:370103	Primary dystonia, DYT17 type	NOT	HP:0002120	ORPHA:370103	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000175	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000316	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000336	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000365	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000431	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000494	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000674	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0000677	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0001256	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0001376	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0001852	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0002652	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0005280	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0010109	ORPHA:90650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0002684	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0002738	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0003042	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0004279	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0005916	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0006487	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0009623	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0009778	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0009882	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0011001	ORPHA:90650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0001850	ORPHA:90650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0005048	ORPHA:90650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90650	Otopalatodigital syndrome type 1		HP:0005640	ORPHA:90650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0001265	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0001288	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0001761	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0002460	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0002936	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0003202	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0003431	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0003448	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0003701	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0007108	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0010871	ORPHA:101081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0002141	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0002751	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0003401	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0007131	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0008981	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0009113	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0010833	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0030834	ORPHA:101081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101081	Charcot-Marie-Tooth disease type 1A		HP:0006801	ORPHA:101081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000160	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000175	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000239	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000272	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000316	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000336	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000337	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000365	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000369	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000377	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000494	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000674	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000677	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000774	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002089	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002652	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0003196	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0005280	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0006487	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0009778	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0010109	ORPHA:90652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000047	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000126	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000162	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000201	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000238	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000347	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000772	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001249	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001263	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001321	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001508	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001539	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001654	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001671	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002684	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002738	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002869	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002990	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0003042	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0004279	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0005640	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0005916	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0006000	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0011001	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0100490	ORPHA:90652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0000518	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0001087	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002084	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002475	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0002650	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0005048	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0008368	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0009702	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90652	Otopalatodigital syndrome type 2		HP:0100258	ORPHA:90652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0001324	ORPHA:101082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0000365	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0000615	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0000762	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0001284	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0002650	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0002922	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0003202	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0003236	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0003469	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0003477	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0003712	ORPHA:101082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0001270	ORPHA:101082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101082	Charcot-Marie-Tooth disease type 1B		HP:0003474	ORPHA:101082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000023	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000045	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000158	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000212	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000280	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000303	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000343	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000400	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000455	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000457	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000486	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000618	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000639	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000648	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000940	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000944	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000951	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001250	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001251	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001252	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001257	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001337	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001347	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001387	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001635	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001744	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001824	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002007	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002205	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002230	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002383	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002650	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002652	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002829	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0003307	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0003312	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0004322	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0004345	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0005280	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0005930	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0007325	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0007957	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0008046	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0010318	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0010729	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0100022	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0100490	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0100670	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001627	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002071	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002500	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000924	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0011951	ORPHA:354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0410263	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001638	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0100543	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0025013	ORPHA:354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0008166	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002376	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000943	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002015	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001332	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0040197	ORPHA:354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001508	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0011968	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001288	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002020	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001543	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0011471	ORPHA:354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001290	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0025190	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001263	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001433	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001007	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001789	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002808	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0009826	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000369	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002011	ORPHA:354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000160	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002167	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0012523	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001643	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0000926	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001622	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0500049	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001072	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0002317	ORPHA:354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:354	GM1 gangliosidosis		HP:0001629	ORPHA:354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0000158	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0001667	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0002136	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0002359	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0002515	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0002938	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003236	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003458	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003484	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003551	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003557	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003691	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003707	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003730	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0004311	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0008981	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0009046	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0030007	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0100284	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0100297	ORPHA:353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0000276	ORPHA:353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0001771	ORPHA:353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0002650	ORPHA:353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003391	ORPHA:353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0003722	ORPHA:353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0025169	ORPHA:353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353	Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5		HP:0030051	ORPHA:353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0000273	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0000713	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0000733	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0001259	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0002039	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0002300	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0002533	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0007302	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0010529	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0100753	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0410291	ORPHA:648919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0000752	ORPHA:648919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0002396	ORPHA:648919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0025401	ORPHA:648919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0030903	ORPHA:648919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648919	Idiopathic catatonia		HP:0100710	ORPHA:648919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0002066	ORPHA:356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0007340	ORPHA:356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0012534	ORPHA:356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0100543	ORPHA:356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0000726	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0001260	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0001268	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0001284	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0001315	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0001317	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0002062	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0002071	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0002360	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0003401	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0011730	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0031006	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0410263	ORPHA:356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356	Gerstmann-Straussler-Scheinker syndrome		HP:0045084	ORPHA:356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001928	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002071	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002092	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002093	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002119	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002179	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002206	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002754	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002756	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002758	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002797	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002804	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002808	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0003233	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0003459	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0004322	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0004374	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0004380	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0004382	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0006530	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0006775	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0006824	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0007141	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0007957	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0008064	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0010702	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0010729	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0011001	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0011227	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0012115	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0031047	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001399	ORPHA:355	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0012223	ORPHA:355	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0034336	ORPHA:355	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001744	ORPHA:355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001903	ORPHA:355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002240	ORPHA:355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0003656	ORPHA:355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0012378	ORPHA:355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000486	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000716	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000823	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000924	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000938	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001081	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001249	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001251	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001373	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001510	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001873	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001882	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001945	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002015	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002027	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002069	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002123	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002376	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002653	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002750	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002757	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0002829	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0003281	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0003330	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0004975	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0008872	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0010885	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0032640	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0100022	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:6000213	ORPHA:355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000093	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000225	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000238	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000365	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000488	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000657	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000726	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000790	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0000939	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001000	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001103	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001252	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001300	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001337	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001387	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001394	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001395	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001522	ORPHA:355	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001637	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001654	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001697	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001789	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001876	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:355	Gaucher disease		HP:0001892	ORPHA:355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000708	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001257	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001288	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002401	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002497	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002634	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0003418	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0007024	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0008480	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0012514	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0030892	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0040161	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0100543	ORPHA:199354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000712	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000718	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000726	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000737	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000741	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001268	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001269	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001297	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002063	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002293	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002506	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0003474	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0007256	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0012671	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0012672	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0030833	ORPHA:199354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002069	ORPHA:199354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002751	ORPHA:199354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199354	Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy	NOT	HP:0003657	ORPHA:199354	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0008162	ORPHA:35878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0012051	ORPHA:35878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0000825	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0001263	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0001328	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0002121	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0002197	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0002342	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0007018	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0008283	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0011198	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35878	Hyperinsulinism-hyperammonemia syndrome		HP:0012402	ORPHA:35878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0001284	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0001288	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0001761	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0002378	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0002936	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0003376	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0003431	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0003444	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0008944	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0008954	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0009027	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0009053	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0011399	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0011727	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0030237	ORPHA:101076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0000407	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0000543	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0001138	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0001249	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0001265	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0001347	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0002313	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0003487	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0006801	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0007924	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101076	X-linked Charcot-Marie-Tooth disease type 2		HP:0031866	ORPHA:101076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001270	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001284	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001288	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001760	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001761	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001288	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0003431	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0003474	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0003693	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0007141	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0008110	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0008944	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0008954	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0009027	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0009063	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0030237	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0031936	ORPHA:101077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001265	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001337	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0001385	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0002091	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0002540	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0002650	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0003477	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0007108	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0007149	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0008081	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101077	X-linked Charcot-Marie-Tooth disease type 3		HP:0008994	ORPHA:101077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0000365	ORPHA:101078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0000762	ORPHA:101078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0000763	ORPHA:101078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0001249	ORPHA:101078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0001251	ORPHA:101078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0001284	ORPHA:101078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0001288	ORPHA:101078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0001337	ORPHA:101078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0001761	ORPHA:101078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0002360	ORPHA:101078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0002460	ORPHA:101078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0002650	ORPHA:101078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0002808	ORPHA:101078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0003202	ORPHA:101078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0007141	ORPHA:101078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101078	X-linked Charcot-Marie-Tooth disease type 4		HP:0007328	ORPHA:101078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0000338	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0000571	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0000658	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001257	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001260	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001337	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001347	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002015	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002063	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002067	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002145	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002172	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002185	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002312	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0002548	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0004373	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0006892	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0007058	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0007153	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0010522	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0025262	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0040081	ORPHA:199351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0000605	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0000716	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0000746	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0000751	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001250	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001263	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001332	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0001336	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0011999	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199351	Adult-onset dystonia-parkinsonism		HP:0012675	ORPHA:199351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0000280	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0000365	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0000925	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0001249	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0001250	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0002652	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0003468	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0007957	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:351	Galactosialidosis		HP:0010729	ORPHA:351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46532	Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome		HP:0000980	ORPHA:46532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46532	Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome		HP:0001744	ORPHA:46532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46532	Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome		HP:0001903	ORPHA:46532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46532	Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome		HP:0002240	ORPHA:46532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46532	Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome		HP:0003330	ORPHA:46532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46532	Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome		HP:0011904	ORPHA:46532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0000708	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0000709	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0000716	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0000737	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0000739	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0001250	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0001254	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0001268	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0001945	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0002315	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0002922	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0010843	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0012229	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0012658	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0033687	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:5000016	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:5000020	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:6000397	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:6001115	ORPHA:623615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:0010532	ORPHA:623615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:5000005	ORPHA:623615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis		HP:5000010	ORPHA:623615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis	NOT	HP:0002383	ORPHA:623615	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:623615	Autoimmune limbic encephalitis	NOT	HP:0100836	ORPHA:623615	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000217	ORPHA:289390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001097	ORPHA:289390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000077	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000707	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000739	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000951	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001970	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002829	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0003011	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0004431	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0005195	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0011850	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0012378	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0012532	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0031950	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0033555	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0034064	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0034066	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0034069	ORPHA:289390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000083	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000099	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000708	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000716	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000958	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000965	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000979	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001045	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001250	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001287	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001317	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001324	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001369	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001871	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001873	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001882	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001888	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001895	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0001897	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002011	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002613	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002633	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002665	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002716	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0003326	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0003474	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0004302	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0004313	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0032218	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0005421	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0005523	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0006527	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0006530	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0006536	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0010702	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0012089	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0012219	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0012387	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0020151	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0030880	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0031088	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0031246	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0031452	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0031983	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0034076	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0034093	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0045042	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0100614	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0100646	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0100653	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0100778	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0200042	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0200123	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0410008	ORPHA:289390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0000726	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002072	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0002143	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0007141	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0009830	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0032018	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0100543	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0100583	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289390	Primary Sjögren disease		HP:0200120	ORPHA:289390	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0033792	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000384	ORPHA:141132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0001140	ORPHA:141132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0011332	ORPHA:141132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000347	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000365	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000413	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000750	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0002414	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0002650	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0002937	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0008551	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0009117	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0009118	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0012210	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0012758	ORPHA:141132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000238	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000252	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000568	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000589	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0000678	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0001511	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0001561	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0001627	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0002308	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0002781	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0002870	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0007370	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141132	Oculo-auriculo-vertebral spectrum		HP:0009892	ORPHA:141132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0000763	ORPHA:101075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0001284	ORPHA:101075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0001761	ORPHA:101075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0007149	ORPHA:101075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0008944	ORPHA:101075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0040129	ORPHA:101075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0007328	ORPHA:101075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0000365	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0001251	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0001260	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0001262	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0001288	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0001337	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0002463	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0002650	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101075	X-linked Charcot-Marie-Tooth disease type 1		HP:0002808	ORPHA:101075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000033	ORPHA:347	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000037	ORPHA:347	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0100820	ORPHA:347	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000093	ORPHA:347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000097	ORPHA:347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000786	ORPHA:347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000815	ORPHA:347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000837	ORPHA:347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0008214	ORPHA:347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0008723	ORPHA:347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000083	ORPHA:347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000100	ORPHA:347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000150	ORPHA:347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0000822	ORPHA:347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0010464	ORPHA:347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:347	Frasier syndrome		HP:0002667	ORPHA:347	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:346	Quinquaud folliculitis decalvans		HP:0001581	ORPHA:346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:346	Quinquaud folliculitis decalvans		HP:0001595	ORPHA:346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:346	Quinquaud folliculitis decalvans		HP:0002232	ORPHA:346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:346	Quinquaud folliculitis decalvans		HP:0004552	ORPHA:346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:346	Quinquaud folliculitis decalvans		HP:0010783	ORPHA:346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:346	Quinquaud folliculitis decalvans		HP:0100699	ORPHA:346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:346	Quinquaud folliculitis decalvans		HP:0200039	ORPHA:346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0000164	ORPHA:349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0000248	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0000280	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0000365	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0000821	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0000943	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0000975	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001063	ORPHA:349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001250	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001252	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001257	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001263	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001508	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001597	ORPHA:349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001626	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001640	ORPHA:349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0001999	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0002240	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0002510	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0002808	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0003199	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0005264	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0005595	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0007256	ORPHA:349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0007957	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0008155	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0008430	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0010864	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0011220	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0011276	ORPHA:349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:349	Fucosidosis		HP:0100578	ORPHA:349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0001249	ORPHA:101070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0001250	ORPHA:101070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0001270	ORPHA:101070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0002119	ORPHA:101070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0002539	ORPHA:101070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0007033	ORPHA:101070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0007266	ORPHA:101070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0000565	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0001263	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0001317	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0001320	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0002141	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0002463	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0007256	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0010864	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0012110	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0025190	ORPHA:101070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0000252	ORPHA:101070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0000486	ORPHA:101070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0002123	ORPHA:101070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0002365	ORPHA:101070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0010819	ORPHA:101070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0011147	ORPHA:101070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101070	Bilateral frontoparietal polymicrogyria		HP:0040194	ORPHA:101070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001942	ORPHA:348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001943	ORPHA:348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0003128	ORPHA:348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0012379	ORPHA:348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002013	ORPHA:348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002014	ORPHA:348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002149	ORPHA:348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0003162	ORPHA:348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0004913	ORPHA:348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0000737	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0000980	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001249	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001250	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001252	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001259	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001262	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001397	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001649	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001946	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0001998	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002094	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002098	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002119	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002240	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002329	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002876	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0002910	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0003265	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0004372	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0004879	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0005949	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0006582	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0040301	ORPHA:348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:348	Fructose-1,6-bisphosphatase deficiency		HP:0003348	ORPHA:348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0001249	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0001269	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0002539	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0006872	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0006891	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0006956	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0007359	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0012758	ORPHA:101071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0002069	ORPHA:101071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0011185	ORPHA:101071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0012704	ORPHA:101071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0002123	ORPHA:101071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0012469	ORPHA:101071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101071	Unilateral hemispheric polymicrogyria		HP:0020220	ORPHA:101071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0000979	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001025	ORPHA:343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001063	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001250	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001251	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001263	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001369	ORPHA:343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001376	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001510	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0001954	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002014	ORPHA:343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002027	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002076	ORPHA:343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002239	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002240	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002586	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002633	ORPHA:343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002716	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0002829	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0003261	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0003326	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0003565	ORPHA:343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0005214	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0010783	ORPHA:343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0011107	ORPHA:343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:343	Hyperimmunoglobulinemia D with periodic fever		HP:0200034	ORPHA:343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0001262	ORPHA:33208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0002360	ORPHA:33208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0100786	ORPHA:33208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0000736	ORPHA:33208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0002354	ORPHA:33208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0033630	ORPHA:33208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:6000456	ORPHA:33208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0000716	ORPHA:33208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0002519	ORPHA:33208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0006896	ORPHA:33208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0025233	ORPHA:33208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33208	Idiopathic hypersomnia		HP:0025267	ORPHA:33208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002019	ORPHA:342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002027	ORPHA:342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002829	ORPHA:342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0003326	ORPHA:342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000093	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000737	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001055	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001250	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001369	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001974	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002014	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002102	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002360	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002745	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0004396	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0005764	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0010783	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0011899	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0012378	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0025406	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0033748	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0100749	ORPHA:342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000100	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000112	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000121	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000716	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000739	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0000988	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001287	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001541	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001658	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001733	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001744	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002024	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002586	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002633	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002716	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002758	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0003419	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0003565	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0005214	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0005244	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001945	ORPHA:342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0002017	ORPHA:342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0006554	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0010741	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0011034	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0011675	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0100796	ORPHA:342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:342	Familial Mediterranean fever		HP:0001701	ORPHA:342	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:345	Dissecting cellulitis of the scalp		HP:0000969	ORPHA:345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:345	Dissecting cellulitis of the scalp		HP:0000989	ORPHA:345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:345	Dissecting cellulitis of the scalp		HP:0001482	ORPHA:345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:345	Dissecting cellulitis of the scalp		HP:0001581	ORPHA:345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:345	Dissecting cellulitis of the scalp		HP:0001595	ORPHA:345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:345	Dissecting cellulitis of the scalp		HP:0100658	ORPHA:345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:345	Dissecting cellulitis of the scalp		HP:0100809	ORPHA:345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0000127	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0000407	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0000848	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0000859	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001249	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001250	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001251	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001263	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0002197	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0002900	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0002917	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0005567	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0012591	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0012606	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0030083	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0200114	ORPHA:199343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0000805	ORPHA:199343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001959	ORPHA:199343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0002345	ORPHA:199343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001272	ORPHA:199343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001344	ORPHA:199343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0001288	ORPHA:199343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0002540	ORPHA:199343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0003477	ORPHA:199343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0007182	ORPHA:199343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199343	EAST syndrome		HP:0007340	ORPHA:199343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001919	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001945	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0003259	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0011037	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0012213	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0030005	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0032169	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0100520	ORPHA:340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000093	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000099	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000622	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000967	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001262	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001324	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001649	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001873	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001962	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001970	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001974	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002013	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002018	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002027	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002315	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002615	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0003326	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0003418	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0004325	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0004729	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0012378	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0025143	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0030783	ORPHA:340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000713	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000790	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000975	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001289	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001903	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002014	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002090	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002094	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002098	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002153	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002202	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002248	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002905	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002910	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0011896	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0012735	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0031273	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0031364	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0100519	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0100598	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0100785	ORPHA:340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000421	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0000822	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0001259	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002170	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002249	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0002878	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0011029	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:340	Hemorrhagic fever-renal syndrome		HP:0012622	ORPHA:340	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia		HP:0030688	ORPHA:438274	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia		HP:0001081	ORPHA:438274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia		HP:0002027	ORPHA:438274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia		HP:0002894	ORPHA:438274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia		HP:0012440	ORPHA:438274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia		HP:0030404	ORPHA:438274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia	NOT	HP:0000819	ORPHA:438274	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia	NOT	HP:0002044	ORPHA:438274	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia	NOT	HP:0010280	ORPHA:438274	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:438274	GCGR-related hyperglucagonemia	NOT	HP:0031181	ORPHA:438274	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0005143	ORPHA:99050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0030680	ORPHA:99050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0000961	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001508	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001631	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001635	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001643	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0002205	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0002875	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0012382	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0032092	ORPHA:99050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001629	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001636	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001669	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0002092	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0011604	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0011661	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0012303	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0030148	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0031632	ORPHA:99050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0001680	ORPHA:99050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0002089	ORPHA:99050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0004383	ORPHA:99050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0004935	ORPHA:99050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0012020	ORPHA:99050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99050	Abnormal origin of right or left pulmonary artery from the aorta		HP:0031934	ORPHA:99050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0001251	ORPHA:623626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0002922	ORPHA:623626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0012229	ORPHA:623626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:6000397	ORPHA:623626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0000639	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0000651	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0001260	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0001272	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0002015	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0002017	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0002315	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0002317	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0011134	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0012189	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0033834	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0100013	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0100543	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:0100615	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:5000006	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:5000016	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:5000024	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:5000030	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:5000034	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623626	Paraneoplastic cerebellar degeneration		HP:5000037	ORPHA:623626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000505	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000543	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000544	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000648	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000649	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000758	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000762	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001250	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001257	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001270	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001272	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001324	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001347	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002015	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002353	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002376	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002521	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0004302	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0005484	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0008936	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0011968	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0012087	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0012696	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0012736	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0012751	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0025112	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0040288	ORPHA:485421	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001510	ORPHA:485421	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485421	MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0011097	ORPHA:485421	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0001612	ORPHA:141127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0001561	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002098	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002778	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0005607	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0011661	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0030680	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0030828	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0030923	ORPHA:141127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0000069	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0000077	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0000119	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0000363	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0000961	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0001562	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0001629	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0001643	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0001791	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002023	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002088	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002094	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002101	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002245	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002247	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002575	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002577	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0004935	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0005151	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0012718	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0012768	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0031935	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0100867	ORPHA:141127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0000707	ORPHA:141127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0002781	ORPHA:141127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0004383	ORPHA:141127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141127	Congenital tracheal stenosis		HP:0025426	ORPHA:141127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0001004	ORPHA:79452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0000034	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0000962	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0001785	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0002619	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0002624	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0003550	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0010741	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0100658	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0100797	ORPHA:79452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0000286	ORPHA:79452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0000708	ORPHA:79452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0001328	ORPHA:79452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0008069	ORPHA:79452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0100725	ORPHA:79452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0200058	ORPHA:79452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0001055	ORPHA:79452	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79452	Milroy disease		HP:0001999	ORPHA:79452	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0000054	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0000225	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0000519	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0000568	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0000961	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0000978	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0001649	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0001667	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0001712	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0001892	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0001933	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0001945	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0002027	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0002179	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0002580	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0007185	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0008151	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0008734	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0009723	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0011029	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0011884	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0012223	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0012886	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0030680	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0100759	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:335	Congenital fibrinogen deficiency		HP:0100845	ORPHA:335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0025081	ORPHA:79455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0000989	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0001034	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0002014	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0012733	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0025473	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0025533	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0030350	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0040186	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0200035	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0200036	ORPHA:79455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0000953	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0001072	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0002013	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0002018	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0002027	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0002094	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0002315	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0002615	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0008066	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0010783	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0031284	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0031901	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0040189	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0100585	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0200041	ORPHA:79455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0007583	ORPHA:79455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0011971	ORPHA:79455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0100665	ORPHA:79455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma		HP:0100845	ORPHA:79455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79455	Cutaneous mastocytoma	NOT	HP:0002716	ORPHA:79455	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0001743	ORPHA:79456	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002716	ORPHA:79456	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0005547	ORPHA:79456	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0005561	ORPHA:79456	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0000989	ORPHA:79456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0011354	ORPHA:79456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0025081	ORPHA:79456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0031284	ORPHA:79456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0031901	ORPHA:79456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0001025	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0001072	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002013	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002014	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002315	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002615	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0004395	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0008066	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0025533	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0100827	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0100845	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0200041	ORPHA:79456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0001019	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0001392	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0001945	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002027	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002239	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0002240	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0009123	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0011971	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0030828	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79456	Diffuse cutaneous mastocytosis		HP:0040189	ORPHA:79456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0011986	ORPHA:337	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001376	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001482	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001844	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0002949	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0003306	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0003468	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0010054	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0010109	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0011987	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0011989	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0030431	ORPHA:337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0000365	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001172	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001385	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001596	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0002093	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0002650	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0002659	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0003367	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0010058	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0030084	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0030838	ORPHA:337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0000787	ORPHA:337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001004	ORPHA:337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001508	ORPHA:337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001822	ORPHA:337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0002625	ORPHA:337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0030038	ORPHA:337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0100240	ORPHA:337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0000501	ORPHA:337	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001249	ORPHA:337	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001250	ORPHA:337	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0001903	ORPHA:337	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:337	Fibrodysplasia ossificans progressiva		HP:0002750	ORPHA:337	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0100845	ORPHA:79457	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0011354	ORPHA:79457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0025081	ORPHA:79457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0000989	ORPHA:79457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0010783	ORPHA:79457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0012733	ORPHA:79457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0025507	ORPHA:79457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0000737	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0001945	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0002013	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0002014	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0002018	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0002027	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0002315	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0002653	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0008066	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0011971	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0020172	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0031284	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0031901	ORPHA:79457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79457	Maculopapular cutaneous mastocytosis		HP:0002094	ORPHA:79457	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0000028	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0000175	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0000218	ORPHA:376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0000324	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0000365	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0000767	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0001376	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0001883	ORPHA:376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0002650	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0003199	ORPHA:376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0004209	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0004322	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0006101	ORPHA:376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:376	Gordon syndrome		HP:0100490	ORPHA:376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0000083	ORPHA:375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0000093	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0000541	ORPHA:375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0000790	ORPHA:375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0000979	ORPHA:375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0001369	ORPHA:375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0001903	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0001945	ORPHA:375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0002093	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0002105	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0002113	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0002633	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0002829	ORPHA:375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0002960	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0003326	ORPHA:375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0006335	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0012735	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0100749	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:375	Anti-glomerular basement membrane disease		HP:0100820	ORPHA:375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000194	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000322	ORPHA:228384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000337	ORPHA:228384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000348	ORPHA:228384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000463	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000486	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000490	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000574	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000582	ORPHA:228384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000609	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000729	ORPHA:228384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000733	ORPHA:228384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0000750	ORPHA:228384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0001250	ORPHA:228384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0001252	ORPHA:228384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0001770	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0002079	ORPHA:228384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0002119	ORPHA:228384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0002335	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0003196	ORPHA:228384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0006913	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0010864	ORPHA:228384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0011968	ORPHA:228384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228384	5q14.3 microdeletion syndrome		HP:0012639	ORPHA:228384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000995	ORPHA:377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002514	ORPHA:377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002664	ORPHA:377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0010610	ORPHA:377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0010612	ORPHA:377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000256	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000431	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000464	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000772	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000892	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000902	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000907	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0001156	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002650	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002671	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002948	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0005462	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0008422	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0010603	ORPHA:377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000028	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000044	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000202	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000238	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000248	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000280	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000286	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000303	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000316	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000486	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000501	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000506	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000518	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000612	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0000670	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0001166	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0001249	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002007	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002858	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002937	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0003468	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0004408	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0005449	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0010618	ORPHA:377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0002885	ORPHA:377	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:377	Gorlin syndrome		HP:0010617	ORPHA:377	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:371	Glycogen storage disease due to muscle phosphofructokinase deficiency		HP:0001324	ORPHA:371	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371	Glycogen storage disease due to muscle phosphofructokinase deficiency		HP:0001903	ORPHA:371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371	Glycogen storage disease due to muscle phosphofructokinase deficiency		HP:0002149	ORPHA:371	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371	Glycogen storage disease due to muscle phosphofructokinase deficiency		HP:0002486	ORPHA:371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371	Glycogen storage disease due to muscle phosphofructokinase deficiency		HP:0003202	ORPHA:371	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371	Glycogen storage disease due to muscle phosphofructokinase deficiency		HP:0009051	ORPHA:371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0012418	ORPHA:685082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0000765	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0000961	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0001622	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0002789	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0002878	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0030863	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0100598	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0100750	ORPHA:685082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0001649	ORPHA:685082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0001662	ORPHA:685082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0001695	ORPHA:685082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0002090	ORPHA:685082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0002615	ORPHA:685082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0011947	ORPHA:685082	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:685082	Pediatric acute respiratory distress syndrome		HP:0100806	ORPHA:685082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000003	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000028	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000098	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000154	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000158	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000256	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000280	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000303	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000316	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000772	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001162	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001629	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001744	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001769	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001773	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001831	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002240	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002558	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002948	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0003212	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0003422	ORPHA:373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000023	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000072	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000073	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000126	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000175	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000358	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000431	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000463	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000465	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000470	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000494	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000767	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001522	ORPHA:373	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001537	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001539	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001561	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001631	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001657	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001770	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001792	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001943	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002164	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002167	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002650	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002705	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0003196	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0004209	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0006101	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0009536	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0010318	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0011039	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0011304	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0011710	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0030680	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0100490	ORPHA:373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000047	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000204	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000286	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0000776	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001249	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001250	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001252	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001263	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001274	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001305	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001374	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001608	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001609	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001638	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001748	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0001762	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002664	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002667	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0002884	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0003006	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0004510	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0005616	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:373	Simpson-Golabi-Behmel syndrome		HP:0008736	ORPHA:373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0000790	ORPHA:329918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0000093	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0000793	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0000822	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0003259	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0003774	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0005421	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0012574	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0012622	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0025364	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0030888	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0031047	ORPHA:329918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0000100	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0000572	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0001919	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0002719	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0002960	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0009125	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0011510	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0025567	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0030469	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0030506	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329918	C3 glomerulopathy		HP:0045042	ORPHA:329918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000737	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000739	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000815	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000822	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000876	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0001265	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0001266	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0001289	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0001657	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002094	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002176	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002514	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003394	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003401	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003472	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003739	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003761	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0004305	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0004349	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0004438	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0009642	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0010041	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0011458	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0011869	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0012049	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0025027	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0100749	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002199	ORPHA:79443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003528	ORPHA:79443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000852	ORPHA:79443	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000311	ORPHA:79443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002901	ORPHA:79443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002905	ORPHA:79443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003165	ORPHA:79443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0003456	ORPHA:79443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0004322	ORPHA:79443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0008227	ORPHA:79443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000293	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000470	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000518	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000639	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000684	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000824	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0001156	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0001249	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0001513	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002135	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002591	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0002684	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0004704	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0005280	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0006297	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0006960	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0010027	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0010044	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0010047	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0010049	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0010743	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0011001	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0011986	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0012185	ORPHA:79443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000407	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000486	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000509	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000585	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0000716	ORPHA:79443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A		HP:0008202	ORPHA:79443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79443	Pseudohypoparathyroidism type 1A	NOT	HP:0030057	ORPHA:79443	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0000938	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0000939	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001508	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0002240	ORPHA:369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0006568	ORPHA:369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0000823	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001510	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001943	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001946	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0002910	ORPHA:369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0000737	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001252	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001270	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001395	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0002360	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0003077	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0003270	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0003710	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0004322	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0004913	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0006580	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0030973	ORPHA:369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0000077	ORPHA:369	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0000093	ORPHA:369	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001394	ORPHA:369	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001402	ORPHA:369	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0001639	ORPHA:369	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369	Glycogen storage disease due to liver glycogen phosphorylase deficiency		HP:0011997	ORPHA:369	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000852	ORPHA:79444	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0002901	ORPHA:79444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0002905	ORPHA:79444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0003165	ORPHA:79444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0003456	ORPHA:79444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0008227	ORPHA:79444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000293	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000311	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000470	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000518	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000639	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000684	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000824	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0001156	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0001249	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0001513	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0002135	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0002591	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0004322	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0004704	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0005280	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0006297	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0006960	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0010044	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0010047	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0010049	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0010743	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0011986	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0012185	ORPHA:79444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000509	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000716	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000737	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000739	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000815	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0000876	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0001265	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0001289	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0001657	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0002094	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0002514	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0003394	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0003401	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0003472	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0003739	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0003761	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0009642	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0010041	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0011001	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0011458	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0012049	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0025027	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0100749	ORPHA:79444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0002199	ORPHA:79444	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C		HP:0008202	ORPHA:79444	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79444	Pseudohypoparathyroidism type 1C	NOT	HP:0030057	ORPHA:79444	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0003236	ORPHA:368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0003546	ORPHA:368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0009051	ORPHA:368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0030231	ORPHA:368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0030234	ORPHA:368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0003201	ORPHA:368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0003652	ORPHA:368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0003710	ORPHA:368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0008305	ORPHA:368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0040319	ORPHA:368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0001324	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0001639	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0001649	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0001919	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0002875	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0003202	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0003738	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0008967	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0009073	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0012378	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0030973	ORPHA:368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0002015	ORPHA:368	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0005216	ORPHA:368	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:368	Glycogen storage disease due to muscle glycogen phosphorylase deficiency		HP:0012622	ORPHA:368	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0000311	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0001156	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0004322	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0009237	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0010044	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0010047	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0010743	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0011986	ORPHA:79445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0000750	ORPHA:79445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0001249	ORPHA:79445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0001511	ORPHA:79445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0001513	ORPHA:79445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0004180	ORPHA:79445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0009650	ORPHA:79445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism		HP:0025027	ORPHA:79445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism	NOT	HP:0002901	ORPHA:79445	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism	NOT	HP:0002905	ORPHA:79445	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79445	Pseudopseudohypoparathyroidism	NOT	HP:0003165	ORPHA:79445	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0000750	ORPHA:141152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0002094	ORPHA:141152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0011470	ORPHA:141152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0011968	ORPHA:141152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0000171	ORPHA:141152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0000347	ORPHA:141152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0001824	ORPHA:141152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0002098	ORPHA:141152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0002781	ORPHA:141152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0006265	ORPHA:141152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0011471	ORPHA:141152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0000175	ORPHA:141152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0005483	ORPHA:141152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0010566	ORPHA:141152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0011951	ORPHA:141152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141152	Isolated congenital hypoglossia/aglossia		HP:0012478	ORPHA:141152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001324	ORPHA:365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0009073	ORPHA:365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0010471	ORPHA:365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0034932	ORPHA:365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000338	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000750	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001265	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001270	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001284	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001308	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001508	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001510	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001640	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001712	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002093	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002205	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002240	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001288	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002747	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002875	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003236	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003326	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003391	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003458	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003546	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003551	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0007340	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0008872	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0011947	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0012378	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0025435	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0030148	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0030231	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0031964	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0100595	ORPHA:365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000158	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000183	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000297	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000365	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000508	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0000939	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001260	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001639	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002015	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002098	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002326	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002540	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002633	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002650	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002878	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003307	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0003324	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0004944	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0005165	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0005216	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0006824	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0008947	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0009113	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0010535	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0012532	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0012727	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0012764	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0030195	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0030196	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0031310	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0032092	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:3000062	ORPHA:365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0001371	ORPHA:365	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0002607	ORPHA:365	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0007002	ORPHA:365	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0100543	ORPHA:365	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:365	Glycogen storage disease due to acid maltase deficiency		HP:0100750	ORPHA:365	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0000293	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0000991	ORPHA:364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0001250	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0001252	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0001943	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0002149	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0002205	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0002719	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0003077	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0004322	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364	Glycogen storage disease due to glucose-6-phosphatase deficiency		HP:0100543	ORPHA:364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001410	ORPHA:367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0002240	ORPHA:367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0011354	ORPHA:367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0012269	ORPHA:367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0031331	ORPHA:367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0500032	ORPHA:367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001270	ORPHA:367	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001290	ORPHA:367	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001508	ORPHA:367	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001644	ORPHA:367	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0002910	ORPHA:367	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0003073	ORPHA:367	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0003198	ORPHA:367	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001371	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001394	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001399	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001409	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001433	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001541	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001561	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001635	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001790	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0001989	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0002040	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0002093	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0002098	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0003202	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0003645	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0006829	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:367	Glycogen storage disease due to glycogen branching enzyme deficiency		HP:0008151	ORPHA:367	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:366	Glycogen storage disease due to glycogen debranching enzyme deficiency		HP:0000293	ORPHA:366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:366	Glycogen storage disease due to glycogen debranching enzyme deficiency		HP:0001256	ORPHA:366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:366	Glycogen storage disease due to glycogen debranching enzyme deficiency		HP:0001943	ORPHA:366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:366	Glycogen storage disease due to glycogen debranching enzyme deficiency		HP:0002155	ORPHA:366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:366	Glycogen storage disease due to glycogen debranching enzyme deficiency		HP:0002721	ORPHA:366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:366	Glycogen storage disease due to glycogen debranching enzyme deficiency		HP:0003198	ORPHA:366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:366	Glycogen storage disease due to glycogen debranching enzyme deficiency		HP:0004322	ORPHA:366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000308	ORPHA:228396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000327	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000340	ORPHA:228396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000343	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000358	ORPHA:228396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000377	ORPHA:228396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000463	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000496	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000506	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000508	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000561	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0000574	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0001092	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0002553	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0004209	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0004422	ORPHA:228396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0005180	ORPHA:228396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228396	Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome		HP:0012471	ORPHA:228396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000083	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000225	ORPHA:33226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000365	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000421	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000520	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000573	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000965	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000979	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0000980	ORPHA:33226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001025	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001251	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001297	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001635	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001744	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001874	ORPHA:33226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001897	ORPHA:33226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001909	ORPHA:33226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0001945	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002014	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002024	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002039	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002076	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002093	ORPHA:33226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002113	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002202	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002239	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002240	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002321	ORPHA:33226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002354	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002633	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002665	ORPHA:33226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002716	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0002719	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0003565	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0004372	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0005508	ORPHA:33226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0006824	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0008046	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0009830	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0010741	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0010841	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0012378	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0100539	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0100724	ORPHA:33226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33226	Waldenström macroglobulinemia		HP:0100778	ORPHA:33226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000826	ORPHA:361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0004319	ORPHA:361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0025451	ORPHA:361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000010	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000027	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000851	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0001249	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0001325	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0001639	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002445	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0100618	ORPHA:361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency	NOT	HP:0002960	ORPHA:361	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000846	ORPHA:361	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0008163	ORPHA:361	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0001508	ORPHA:361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002615	ORPHA:361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0007440	ORPHA:361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0011043	ORPHA:361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0012734	ORPHA:361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0031076	ORPHA:361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0031214	ORPHA:361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000127	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0001824	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002013	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002014	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002019	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002039	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002153	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002173	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002574	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002719	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0002902	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0012432	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0012605	ORPHA:361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000028	ORPHA:361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:361	Familial glucocorticoid deficiency		HP:0000098	ORPHA:361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0012378	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0012638	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0001250	ORPHA:360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0002354	ORPHA:360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0012174	ORPHA:360	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0025461	ORPHA:360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0000572	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0000712	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0001273	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0001324	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0002181	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0002315	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0002463	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0002500	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:360	Glioblastoma		HP:0003470	ORPHA:360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000076	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000160	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000232	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000248	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000286	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000343	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000407	ORPHA:228399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000431	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000506	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0000637	ORPHA:228399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0001252	ORPHA:228399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0001263	ORPHA:228399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0001291	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0001629	ORPHA:228399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0001631	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0001773	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0002020	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0002553	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0007018	ORPHA:228399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228399	8q12 microduplication syndrome		HP:0009921	ORPHA:228399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0007359	ORPHA:101046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0008765	ORPHA:101046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0011185	ORPHA:101046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0002381	ORPHA:101046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0011182	ORPHA:101046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0002349	ORPHA:101046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0002367	ORPHA:101046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0011154	ORPHA:101046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0012332	ORPHA:101046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0031951	ORPHA:101046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0000708	ORPHA:101046	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0000716	ORPHA:101046	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0002069	ORPHA:101046	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0002076	ORPHA:101046	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0002197	ORPHA:101046	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0007334	ORPHA:101046	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features		HP:0100710	ORPHA:101046	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features	NOT	HP:0001249	ORPHA:101046	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:101046	Epilepsy with auditory features	NOT	HP:0410263	ORPHA:101046	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000028	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000046	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000135	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000164	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000248	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000289	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000316	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000369	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000430	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000463	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000486	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000506	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000568	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000582	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000639	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0000698	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0001256	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0001274	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0001362	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0001511	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0001562	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0001596	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0002007	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0002084	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0002213	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0002335	ORPHA:228390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0002342	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0004440	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0005280	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228390	Frontonasal dysplasia-alopecia-genital anomalies syndrome		HP:0011803	ORPHA:228390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0030114	ORPHA:178400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0040081	ORPHA:178400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0003738	ORPHA:178400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0008963	ORPHA:178400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0009073	ORPHA:178400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0003325	ORPHA:178400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0003438	ORPHA:178400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0008954	ORPHA:178400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0009005	ORPHA:178400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset		HP:0031177	ORPHA:178400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset	NOT	HP:0000467	ORPHA:178400	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset	NOT	HP:0003474	ORPHA:178400	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:178400	Distal myopathy with anterior tibial onset	NOT	HP:0003805	ORPHA:178400	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000639	ORPHA:79430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001010	ORPHA:79430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001875	ORPHA:79430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001892	ORPHA:79430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002721	ORPHA:79430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0007443	ORPHA:79430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0007730	ORPHA:79430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000083	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000421	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000483	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000486	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000518	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000545	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000587	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000613	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000646	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000649	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000978	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001107	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002206	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0005599	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0400008	ORPHA:79430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000505	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000527	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000682	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000962	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0000995	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001072	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001638	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001824	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0001872	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002024	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002027	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002039	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002094	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002239	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0002671	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0006739	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79430	Hermansky-Pudlak syndrome		HP:0012378	ORPHA:79430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101041	Familial hypofibrinogenemia		HP:0000225	ORPHA:101041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101041	Familial hypofibrinogenemia		HP:0000421	ORPHA:101041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101041	Familial hypofibrinogenemia		HP:0001892	ORPHA:101041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101041	Familial hypofibrinogenemia		HP:0002239	ORPHA:101041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0000505	ORPHA:79431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0000587	ORPHA:79431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0000613	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0000639	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0000649	ORPHA:79431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0000962	ORPHA:79431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0001010	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0001022	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0001072	ORPHA:79431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0001107	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0001480	ORPHA:79431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0002671	ORPHA:79431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0005599	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0006739	ORPHA:79431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0007730	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79431	Oculocutaneous albinism type 1A		HP:0007750	ORPHA:79431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0005323	ORPHA:141145	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0000324	ORPHA:141145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0000689	ORPHA:141145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0001572	ORPHA:141145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0004411	ORPHA:141145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0012471	ORPHA:141145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0100875	ORPHA:141145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0002098	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0002315	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0005216	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0006536	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0009900	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0010807	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0025797	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141145	Hemifacial hyperplasia		HP:0040264	ORPHA:141145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0000539	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0000613	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0000635	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0000639	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0001010	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0001100	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0001480	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0002226	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0005599	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0007663	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0007703	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0007730	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0007750	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0007988	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0011364	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0012805	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0025551	ORPHA:79432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0002227	ORPHA:79432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0002671	ORPHA:79432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0006739	ORPHA:79432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0012056	ORPHA:79432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0030856	ORPHA:79432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0200098	ORPHA:79432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79432	Oculocutaneous albinism type 2		HP:0007481	ORPHA:79432	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002897	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0003201	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0003326	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0003401	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0003470	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0005135	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0005978	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0006789	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0007359	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0009800	ORPHA:358	TAS		HP:0040284			H	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0011736	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0012248	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0012250	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0012364	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0025072	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0030880	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0100324	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0100647	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0100651	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0100785	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002900	ORPHA:358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001324	ORPHA:358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001508	ORPHA:358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001657	ORPHA:358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002027	ORPHA:358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002632	ORPHA:358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002917	ORPHA:358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000017	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000093	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000128	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000805	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000823	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001952	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000855	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002017	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002901	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002918	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0003394	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0030083	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0200114	ORPHA:358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000020	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000097	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000360	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000622	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000872	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000934	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0000975	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001262	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001279	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001663	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001698	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001891	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001947	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001953	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001959	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001962	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001970	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001994	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0001997	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002014	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002019	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002098	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002315	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002321	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002514	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002619	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002829	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:358	Gitelman syndrome		HP:0002894	ORPHA:358	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001251	ORPHA:99027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0012332	ORPHA:99027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001257	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001288	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001324	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001337	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001347	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002066	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002493	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002936	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0003487	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0005341	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0006827	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0006958	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007256	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007366	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007377	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0011931	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0030890	ORPHA:99027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000010	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000012	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000016	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000496	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000639	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000802	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000970	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001260	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001276	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001278	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001310	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0001371	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002015	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002019	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002045	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002064	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002075	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002080	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002169	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002200	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002273	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002345	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002599	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0003326	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0004302	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0004395	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0005968	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0006886	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007351	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007360	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007369	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007370	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0007480	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0010831	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0010845	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0011951	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0100543	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0100639	ORPHA:99027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000407	ORPHA:99027	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000708	ORPHA:99027	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0000726	ORPHA:99027	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99027	Adult-onset autosomal dominant leukodystrophy		HP:0002922	ORPHA:99027	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0000635	ORPHA:79433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0000639	ORPHA:79433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0001010	ORPHA:79433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0001480	ORPHA:79433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0002297	ORPHA:79433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0007730	ORPHA:79433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0011358	ORPHA:79433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0000486	ORPHA:79433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0002226	ORPHA:79433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0002227	ORPHA:79433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0025551	ORPHA:79433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0100814	ORPHA:79433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79433	Oculocutaneous albinism type 3		HP:0200098	ORPHA:79433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0000486	ORPHA:79434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0000505	ORPHA:79434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0000587	ORPHA:79434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0000613	ORPHA:79434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0000639	ORPHA:79434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0000995	ORPHA:79434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0001010	ORPHA:79434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0001022	ORPHA:79434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0001072	ORPHA:79434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0001480	ORPHA:79434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0002671	ORPHA:79434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0002861	ORPHA:79434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0005599	ORPHA:79434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0006739	ORPHA:79434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0007703	ORPHA:79434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0007730	ORPHA:79434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79434	Oculocutaneous albinism type 1B		HP:0007750	ORPHA:79434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0040075	ORPHA:90695	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000044	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000141	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000457	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000789	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000824	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0001510	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0001943	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0002615	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0002920	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0004322	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0008245	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0008734	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0009888	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0010311	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0010627	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0012378	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0040086	ORPHA:90695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000823	ORPHA:90695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000839	ORPHA:90695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0000938	ORPHA:90695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0002019	ORPHA:90695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0002750	ORPHA:90695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0005625	ORPHA:90695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0008187	ORPHA:90695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0011755	ORPHA:90695	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90695	Non-acquired panhypopituitarism		HP:0012731	ORPHA:90695	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0000639	ORPHA:79435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0007663	ORPHA:79435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0007703	ORPHA:79435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0007750	ORPHA:79435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0000613	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0001010	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0001022	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0001072	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0001107	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0005599	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0007730	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0011364	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0025551	ORPHA:79435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0003764	ORPHA:79435	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79435	Oculocutaneous albinism type 4		HP:0008069	ORPHA:79435	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0000822	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001249	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001250	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001251	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001254	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001328	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001950	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002013	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002240	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002329	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002353	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002789	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002910	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0011966	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0012758	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0025630	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0032470	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0032491	ORPHA:23	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0000083	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0000670	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0000709	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0000742	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0000750	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0000964	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001270	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001324	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001332	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001337	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001394	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001395	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001399	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001894	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002014	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002155	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002232	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002283	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0002900	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0003218	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0003777	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0006280	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0006970	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0007018	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0007183	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0009886	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0011362	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0011675	ORPHA:23	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001402	ORPHA:23	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0001987	ORPHA:23	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0003217	ORPHA:23	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0003355	ORPHA:23	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:23	Argininosuccinic aciduria		HP:0005961	ORPHA:23	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0000232	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0000233	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0000252	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0000319	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0000431	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0000455	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0000767	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0001249	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0001270	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0001510	ORPHA:73273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0001511	ORPHA:73273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0002750	ORPHA:73273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0004279	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0004322	ORPHA:73273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0006610	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73273	Growth delay due to insulin-like growth factor I resistance		HP:0030084	ORPHA:73273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0000467	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0000473	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0001263	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0001319	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0001558	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0002460	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0002515	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003236	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003327	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003391	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003458	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003551	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003555	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003701	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003715	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003736	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003798	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003805	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0006785	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0010628	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0012899	ORPHA:97240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97240	Zebra body myopathy		HP:0003713	ORPHA:97240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000252	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000399	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000407	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000708	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000736	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000752	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000855	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001249	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001256	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001508	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001511	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001518	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001999	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0004322	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0007018	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0008527	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0008619	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0008846	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0008850	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0008897	ORPHA:73272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000135	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000153	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000347	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000684	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000939	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0002750	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0003265	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0004209	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0006266	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0030084	ORPHA:73272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000294	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000508	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000545	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000954	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0000957	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001270	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001943	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0001956	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0002162	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0007911	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0011120	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73272	Growth delay due to insulin-like growth factor type 1 deficiency		HP:0011220	ORPHA:73272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0003536	ORPHA:24	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0000316	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001250	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001252	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001254	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001263	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001298	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001531	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001561	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001622	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002007	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002059	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002119	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0005280	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0008872	ORPHA:24	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0000252	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0000463	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0000648	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0000817	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001259	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001273	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001332	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001511	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001562	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001875	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001901	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002013	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002240	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002421	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002500	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0002521	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0003191	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0006808	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0010804	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0012402	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0012448	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0012469	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0025646	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0034648	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0100704	ORPHA:24	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001942	ORPHA:24	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001943	ORPHA:24	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0001987	ORPHA:24	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:24	Fumaric aciduria		HP:0003128	ORPHA:24	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0000962	ORPHA:312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0001019	ORPHA:312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0001824	ORPHA:312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0004396	ORPHA:312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0007475	ORPHA:312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0008064	ORPHA:312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0008066	ORPHA:312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0000992	ORPHA:312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0000982	ORPHA:312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0100780	ORPHA:312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:312	Autosomal dominant epidermolytic ichthyosis		HP:0200042	ORPHA:312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002134	ORPHA:25	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0003150	ORPHA:25	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0012379	ORPHA:25	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0001260	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0001332	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0001334	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002015	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002311	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002305	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002315	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002339	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0004481	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0007132	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0009716	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0011968	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0012704	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0012753	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0031982	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0040194	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0100954	ORPHA:25	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0000573	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0000726	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0001250	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0001251	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0001337	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0001373	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002063	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002072	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002086	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002119	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002321	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002376	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002451	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0002500	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0003162	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0003546	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0006829	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0007185	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0012469	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0100309	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0100543	ORPHA:25	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0009830	ORPHA:25	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:25	Glutaryl-CoA dehydrogenase deficiency		HP:0012622	ORPHA:25	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0000252	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0000488	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0000646	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001249	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001250	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001252	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001254	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001263	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001508	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001980	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0011968	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0012378	ORPHA:26	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0000238	ORPHA:26	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0000708	ORPHA:26	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0001288	ORPHA:26	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0030680	ORPHA:26	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0100022	ORPHA:26	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26	Methylmalonic acidemia with homocystinuria		HP:0000988	ORPHA:26	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0002373	ORPHA:101039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000708	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000718	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000722	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000739	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000750	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0001249	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0001270	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0002069	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0002133	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0010818	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0011169	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0012433	ORPHA:101039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000729	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000752	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0001256	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0001263	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0002121	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0002123	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0002187	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0002342	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0007270	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0007359	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0010819	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0010864	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0011172	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0100710	ORPHA:101039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0000709	ORPHA:101039	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101039	Female restricted epilepsy with intellectual disability		HP:0100738	ORPHA:101039	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0000467	ORPHA:97244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0001290	ORPHA:97244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0002093	ORPHA:97244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0002650	ORPHA:97244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0003198	ORPHA:97244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0003306	ORPHA:97244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0011842	ORPHA:97244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0001265	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0002090	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0002421	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0002987	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0003089	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0003202	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0003273	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0003307	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0030878	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0031546	ORPHA:97244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0001263	ORPHA:97244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0002515	ORPHA:97244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97244	Rigid spine syndrome		HP:0003391	ORPHA:97244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001336	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001824	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001882	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001894	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001944	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001945	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001942	ORPHA:20	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001958	ORPHA:20	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001987	ORPHA:20	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0003344	ORPHA:20	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0000741	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001250	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001252	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001254	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001903	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001988	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002039	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002149	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002151	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002240	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002353	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002572	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002789	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002910	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0006561	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0006582	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0008151	ORPHA:20	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0000952	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0000969	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0000980	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001256	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001259	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001265	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001298	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001974	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002014	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002104	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002342	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002521	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002615	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002919	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0010864	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0012378	ORPHA:20	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0000252	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001251	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001257	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001260	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001325	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001644	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001695	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0001735	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002045	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0002352	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:20	3-hydroxy-3-methylglutaric aciduria		HP:0011099	ORPHA:20	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0012103	ORPHA:330050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000639	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000648	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001250	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001263	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001344	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002133	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002151	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002376	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002540	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0012707	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0410263	ORPHA:330050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0000486	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001272	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001332	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001337	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001488	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002069	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002123	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0001288	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002381	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002384	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002506	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0002650	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0003202	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0006801	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0007359	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0010553	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0011471	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330050	DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect		HP:0012569	ORPHA:330050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0000708	ORPHA:22	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0001249	ORPHA:22	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0001251	ORPHA:22	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0001252	ORPHA:22	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0001263	ORPHA:22	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0001939	ORPHA:22	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0002069	ORPHA:22	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0002123	ORPHA:22	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:22	Succinic semialdehyde dehydrogenase deficiency		HP:0002133	ORPHA:22	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0000083	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0000648	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001249	ORPHA:27	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001250	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001251	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001252	ORPHA:27	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001254	ORPHA:27	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001259	ORPHA:27	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001263	ORPHA:27	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001266	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001638	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001733	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001873	ORPHA:27	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001882	ORPHA:27	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001903	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001944	ORPHA:27	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001972	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0001987	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0002017	ORPHA:27	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0002093	ORPHA:27	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0002167	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0002240	ORPHA:27	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0002273	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0002385	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:27	Vitamin B12-unresponsive methylmalonic acidemia		HP:0002721	ORPHA:27	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0000083	ORPHA:28	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001249	ORPHA:28	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001252	ORPHA:28	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001254	ORPHA:28	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001259	ORPHA:28	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001263	ORPHA:28	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001508	ORPHA:28	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001903	ORPHA:28	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001944	ORPHA:28	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0001987	ORPHA:28	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0002017	ORPHA:28	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0002093	ORPHA:28	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28	Vitamin B12-responsive methylmalonic acidemia		HP:0002240	ORPHA:28	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000239	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000252	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000268	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000325	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000358	ORPHA:29	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000494	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000518	ORPHA:29	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0000592	ORPHA:29	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0001249	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0001250	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0001251	ORPHA:29	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0001252	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0001263	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0001744	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0002120	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0002750	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29	Mevalonic aciduria		HP:0004322	ORPHA:29	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0001028	ORPHA:141179	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0007466	ORPHA:141179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0007618	ORPHA:141179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0031449	ORPHA:141179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0100585	ORPHA:141179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0001015	ORPHA:141179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0001635	ORPHA:141179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0001873	ORPHA:141179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0031207	ORPHA:141179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0100784	ORPHA:141179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma		HP:0410266	ORPHA:141179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141179	Non-involuting congenital hemangioma	NOT	HP:0012329	ORPHA:141179	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0002197	ORPHA:307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0002392	ORPHA:307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0007000	ORPHA:307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0000153	ORPHA:307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0000496	ORPHA:307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0002121	ORPHA:307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0002373	ORPHA:307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0007207	ORPHA:307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0000718	ORPHA:307	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy		HP:0002133	ORPHA:307	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:307	Juvenile myoclonic epilepsy	NOT	HP:0001249	ORPHA:307	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0011171	ORPHA:306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0011182	ORPHA:306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy	NOT	HP:0002361	ORPHA:306	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy	NOT	HP:0410263	ORPHA:306	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0002372	ORPHA:306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0032807	ORPHA:306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0002104	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0002266	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0002384	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0007334	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0007359	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0010818	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0011153	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0011167	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0011169	ORPHA:306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0000961	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0001276	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0002069	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0002121	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0032678	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0032823	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0032906	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0045084	ORPHA:306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306	Self-limited infantile epilepsy		HP:0002133	ORPHA:306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314802	Short stature due to partial GHR deficiency		HP:0000823	ORPHA:314802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314802	Short stature due to partial GHR deficiency		HP:0002750	ORPHA:314802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314802	Short stature due to partial GHR deficiency		HP:0001510	ORPHA:314802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314802	Short stature due to partial GHR deficiency		HP:0004322	ORPHA:314802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314802	Short stature due to partial GHR deficiency		HP:0001943	ORPHA:314802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314802	Short stature due to partial GHR deficiency		HP:0011800	ORPHA:314802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314802	Short stature due to partial GHR deficiency		HP:0030353	ORPHA:314802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0000408	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0000508	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0000519	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0001252	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0001263	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0001315	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0001583	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0002079	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0003128	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0008936	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0012343	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome		HP:0030089	ORPHA:330054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330054	Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome	NOT	HP:0001324	ORPHA:330054	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0001250	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002085	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002126	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002269	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002282	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002349	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0003330	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0007359	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0011818	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0032046	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0045084	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0430005	ORPHA:101030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0000290	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0001338	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002057	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002367	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002435	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0002475	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0011195	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0012013	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0025373	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0031006	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101030	Subependymal nodular heterotopia		HP:0100022	ORPHA:101030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0001336	ORPHA:308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0002070	ORPHA:308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0002392	ORPHA:308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0007000	ORPHA:308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0001251	ORPHA:308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0001260	ORPHA:308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0002080	ORPHA:308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0000726	ORPHA:308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0000992	ORPHA:308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:308	Progressive myoclonic epilepsy type 1		HP:0001249	ORPHA:308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0001742	ORPHA:137914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0011109	ORPHA:137914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0031416	ORPHA:137914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0000961	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0001363	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0001601	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0001607	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0002098	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0002205	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0002779	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0002781	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0005321	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0011968	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0030215	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0030842	ORPHA:137914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137914	Choanal atresia		HP:0010442	ORPHA:137914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0000951	ORPHA:220402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0001000	ORPHA:220402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0001053	ORPHA:220402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0002015	ORPHA:220402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0002017	ORPHA:220402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0002020	ORPHA:220402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0002092	ORPHA:220402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0002206	ORPHA:220402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0002960	ORPHA:220402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0008366	ORPHA:220402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0009473	ORPHA:220402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0100579	ORPHA:220402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0100585	ORPHA:220402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0100958	ORPHA:220402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220402	Limited cutaneous systemic sclerosis		HP:0200042	ORPHA:220402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0001051	ORPHA:302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0001053	ORPHA:302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0001581	ORPHA:302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0002715	ORPHA:302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0002860	ORPHA:302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0007565	ORPHA:302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0100585	ORPHA:302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0200034	ORPHA:302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0200035	ORPHA:302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0200039	ORPHA:302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:302	Inherited epidermodysplasia verruciformis		HP:0200043	ORPHA:302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0001320	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0001344	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0002079	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0002119	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0002126	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0002350	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0002363	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0002415	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0002421	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0003236	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0007361	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0008947	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0010864	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0011197	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0011344	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0025336	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0030046	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0031882	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0031936	ORPHA:370997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0000518	ORPHA:370997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0000556	ORPHA:370997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0000557	ORPHA:370997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		HP:0011003	ORPHA:370997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0000992	ORPHA:330058	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0032381	ORPHA:330058	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0100699	ORPHA:330058	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0025300	ORPHA:330058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0033700	ORPHA:330058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0000491	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0000613	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0000964	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0002315	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0007663	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0009926	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0010783	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0025337	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0031190	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0031541	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0033834	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme		HP:0100585	ORPHA:330058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330058	Hydroa vacciniforme	NOT	HP:0010473	ORPHA:330058	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:73267	Non-24-hour sleep-wake syndrome		HP:0000618	ORPHA:73267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73267	Non-24-hour sleep-wake syndrome		HP:0000716	ORPHA:73267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73267	Non-24-hour sleep-wake syndrome		HP:0001262	ORPHA:73267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73267	Non-24-hour sleep-wake syndrome		HP:0012689	ORPHA:73267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73267	Non-24-hour sleep-wake syndrome		HP:0025406	ORPHA:73267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0000016	ORPHA:228371	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0000217	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0000508	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0000651	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0001260	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0001324	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0002014	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0002015	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0002017	ORPHA:228371	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0002019	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0002027	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0002747	ORPHA:228371	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0003470	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0006543	ORPHA:228371	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0006597	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0006824	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0011499	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0011675	ORPHA:228371	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228371	Foodborne botulism		HP:0100021	ORPHA:228371	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0001249	ORPHA:35	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0001263	ORPHA:35	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0001638	ORPHA:35	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0001943	ORPHA:35	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0001987	ORPHA:35	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0001992	ORPHA:35	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0002019	ORPHA:35	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0002240	ORPHA:35	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0003353	ORPHA:35	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0010978	ORPHA:35	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35	Propionic acidemia		HP:0011675	ORPHA:35	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000023	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000028	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000047	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000098	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000256	ORPHA:36	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000260	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000269	ORPHA:36	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000316	ORPHA:36	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000340	ORPHA:36	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000407	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000776	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0000889	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0001162	ORPHA:36	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0001199	ORPHA:36	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0001305	ORPHA:36	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0007360	ORPHA:36	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0007370	ORPHA:36	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36	Acrocallosal syndrome		HP:0010864	ORPHA:36	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000157	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000206	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000221	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000492	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000498	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000505	ORPHA:37	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000509	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000534	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000613	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000712	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0000958	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0001508	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0001596	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0001597	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0001807	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0001818	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0001824	ORPHA:37	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0002024	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0002028	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0002039	ORPHA:37	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0002120	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0004322	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0004396	ORPHA:37	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0008066	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0008402	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0010783	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0011354	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0100825	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0200020	ORPHA:37	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0200039	ORPHA:37	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37	Acrodermatitis enteropathica		HP:0200042	ORPHA:37	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001394	ORPHA:101028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001433	ORPHA:101028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001873	ORPHA:101028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001903	ORPHA:101028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0010903	ORPHA:101028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0012202	ORPHA:101028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0000056	ORPHA:101028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0000077	ORPHA:101028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0000969	ORPHA:101028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001009	ORPHA:101028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001789	ORPHA:101028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001999	ORPHA:101028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0100678	ORPHA:101028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001263	ORPHA:101028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001631	ORPHA:101028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0001680	ORPHA:101028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0002795	ORPHA:101028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101028	Transaldolase deficiency		HP:0200128	ORPHA:101028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000085	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000158	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000162	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000218	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000219	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000293	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000341	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000343	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000347	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000358	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000378	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000405	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000463	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000527	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000664	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001249	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001263	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001513	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002086	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002553	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0004322	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0011842	ORPHA:444077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000252	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000311	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000365	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001156	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001627	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001629	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001643	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002019	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002020	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0003468	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0006528	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0011471	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0011951	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0100874	ORPHA:444077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000047	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000076	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000407	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000410	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000486	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000494	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000508	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000518	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000520	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000545	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000574	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000646	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000771	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000821	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000824	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0000956	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001231	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001357	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001601	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001607	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001635	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001655	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0001800	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002092	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002099	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002212	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002616	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002645	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002714	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0002779	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0003038	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0003074	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0003196	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0004602	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0006434	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0008388	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0009894	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0009937	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0010535	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0011221	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0025313	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0030043	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444077	Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome		HP:0200055	ORPHA:444077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0000069	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0000316	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0000358	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0000431	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0000494	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0001263	ORPHA:30	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0001385	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0001643	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0001744	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0001903	ORPHA:30	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0002205	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0003218	ORPHA:30	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0003355	ORPHA:30	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0003526	ORPHA:30	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0011840	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30	Hereditary orotic aciduria		HP:0008388	ORPHA:30	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0000238	ORPHA:31	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0000816	ORPHA:31	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0001251	ORPHA:31	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0001263	ORPHA:31	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0001276	ORPHA:31	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0003202	ORPHA:31	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0004322	ORPHA:31	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0010286	ORPHA:31	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0012401	ORPHA:31	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31	Oxoglutaric aciduria		HP:0100022	ORPHA:31	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32	Glutathione synthetase deficiency		HP:0000707	ORPHA:32	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32	Glutathione synthetase deficiency		HP:0001878	ORPHA:32	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32	Glutathione synthetase deficiency		HP:0001996	ORPHA:32	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32	Glutathione synthetase deficiency		HP:0003343	ORPHA:32	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32	Glutathione synthetase deficiency		HP:0010978	ORPHA:32	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000252	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000675	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000679	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000689	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001263	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001321	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001999	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002213	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002650	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0008070	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0045075	ORPHA:444072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001256	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001508	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002079	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002119	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002280	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002465	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002750	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0006511	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0009085	ORPHA:444072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000023	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000028	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000074	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000126	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000343	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000347	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000369	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000431	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000463	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000470	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000486	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000518	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0000954	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001182	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001601	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001629	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0001634	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002365	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002418	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0002509	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0003100	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0003510	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0004970	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0005135	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0006970	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0007068	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0007835	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0008366	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0010864	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0011406	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0011800	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444072	Cerebellar-facial-dental syndrome		HP:0012110	ORPHA:444072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101023	Cleft hard palate		HP:0000163	ORPHA:101023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101023	Cleft hard palate		HP:0002463	ORPHA:101023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101023	Cleft hard palate		HP:0002870	ORPHA:101023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101023	Cleft hard palate		HP:0008872	ORPHA:101023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101023	Cleft hard palate		HP:0000405	ORPHA:101023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001263	ORPHA:33	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001942	ORPHA:33	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001249	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001250	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001252	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001254	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001508	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001987	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0002013	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0002919	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0003128	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0008872	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0031962	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0033111	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0033447	ORPHA:33	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0000750	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001259	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001270	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001289	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001310	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001337	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001735	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001824	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0002045	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0002901	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0007018	ORPHA:33	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0001994	ORPHA:33	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0002453	ORPHA:33	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33	Isovaleric acidemia		HP:0011675	ORPHA:33	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0000159	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0000969	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0000989	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0001025	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0001279	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0002018	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0002315	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0002321	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0030809	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0030828	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0100326	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0100539	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0100665	ORPHA:97230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0002094	ORPHA:97230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0011971	ORPHA:97230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97230	Solar urticaria		HP:0100845	ORPHA:97230	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0001288	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0002094	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0002091	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0002747	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0002792	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003202	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003236	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003458	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003555	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003557	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003722	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003803	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003805	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0008800	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0008978	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0009027	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0012764	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0031237	ORPHA:178464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0002460	ORPHA:178464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0003701	ORPHA:178464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0008963	ORPHA:178464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0008981	ORPHA:178464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0100293	ORPHA:178464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178464	Hereditary myopathy with early respiratory failure		HP:0002527	ORPHA:178464	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0000972	ORPHA:38	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0025092	ORPHA:38	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0025167	ORPHA:38	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0045059	ORPHA:38	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0002955	ORPHA:38	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0025114	ORPHA:38	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0025507	ORPHA:38	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0040162	ORPHA:38	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0006089	ORPHA:38	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0025509	ORPHA:38	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0200035	ORPHA:38	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:38	Acrokeratoelastoidosis of Costa		HP:0002814	ORPHA:38	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0001250	ORPHA:101029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0002269	ORPHA:101029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0002538	ORPHA:101029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0032391	ORPHA:101029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0001257	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0001324	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0001328	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0001347	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0002126	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0002699	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0010843	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0011193	ORPHA:101029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0001274	ORPHA:101029	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0002079	ORPHA:101029	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101029	Sub-cortical nodular heterotopia		HP:0002134	ORPHA:101029	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000750	ORPHA:171829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0001263	ORPHA:171829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0001513	ORPHA:171829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0001999	ORPHA:171829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000256	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000293	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000341	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000486	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000582	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0001319	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0001328	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0002033	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0002591	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0007874	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0025160	ORPHA:171829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000278	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000337	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000347	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000369	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000414	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000463	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000478	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000574	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000729	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0000765	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0001182	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0001833	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0002136	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0002311	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0005280	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0008551	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171829	6q16 microdeletion syndrome		HP:0031703	ORPHA:171829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000819	ORPHA:99889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0003118	ORPHA:99889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0003154	ORPHA:99889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0003466	ORPHA:99889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0012030	ORPHA:99889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0030200	ORPHA:99889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000141	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000708	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000712	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000739	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000822	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000939	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000953	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000963	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000978	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001007	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001050	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001058	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001061	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001065	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001324	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001626	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001888	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001956	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001974	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002721	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0004324	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0007126	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0008221	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0010284	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0012743	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0025017	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0025383	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0025406	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0030348	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0031364	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0031845	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0031891	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0100785	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0500011	ORPHA:99889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000716	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000725	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000869	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000876	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000979	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001297	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001658	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0001824	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002014	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002039	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002086	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002209	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002354	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002733	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002953	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0006749	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0011370	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0012398	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0030405	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0030446	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0031284	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0031589	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0040270	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0100521	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0100634	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0200042	ORPHA:99889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000709	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0000726	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002666	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0002865	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0006722	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0006725	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0006753	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0010741	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0011999	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0012125	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0025269	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0030357	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0030445	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0100757	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion		HP:0500167	ORPHA:99889	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion	NOT	HP:0002690	ORPHA:99889	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99889	Cushing syndrome due to ectopic ACTH secretion	NOT	HP:0008291	ORPHA:99889	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0000964	ORPHA:330064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0000989	ORPHA:330064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0000992	ORPHA:330064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0025092	ORPHA:330064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0030350	ORPHA:330064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0001053	ORPHA:330064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0007505	ORPHA:330064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0007573	ORPHA:330064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0025127	ORPHA:330064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0100725	ORPHA:330064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0001019	ORPHA:330064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330064	Chronic actinic dermatitis		HP:0003193	ORPHA:330064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0002714	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0002804	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0002919	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0005487	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0005750	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0012594	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0012758	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0000124	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0000365	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001251	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001252	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001259	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0002186	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0002594	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0003477	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0010864	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0010935	ORPHA:99885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus	NOT	HP:0030057	ORPHA:99885	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0000857	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001508	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001824	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001944	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0003074	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0003076	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0006274	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0011106	ORPHA:99885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0000488	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001249	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001263	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001270	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001488	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001511	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0001627	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0002069	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99885	Isolated permanent neonatal diabetes mellitus		HP:0002123	ORPHA:99885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001283	ORPHA:97229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001291	ORPHA:97229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001730	ORPHA:97229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0006824	ORPHA:97229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000496	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000508	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001252	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001260	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001265	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001324	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001336	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0002015	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0002093	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0003202	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0003690	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0010628	ORPHA:97229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000135	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000505	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000543	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000551	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000718	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000738	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000771	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000822	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0000873	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001249	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001250	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001251	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0001337	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0002120	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0004326	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0007730	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0008002	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0010535	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97229	Riboflavin transporter deficiency		HP:0012332	ORPHA:97229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001511	ORPHA:99886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001518	ORPHA:99886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001944	ORPHA:99886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0003074	ORPHA:99886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0040216	ORPHA:99886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0000158	ORPHA:99886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001537	ORPHA:99886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0004904	ORPHA:99886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0008255	ORPHA:99886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0000077	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0000079	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0000365	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0000707	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0000821	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001250	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001252	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001508	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001627	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0009800	ORPHA:99886	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0012758	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0040064	ORPHA:99886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus		HP:0001953	ORPHA:99886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99886	Transient neonatal diabetes mellitus	NOT	HP:0030057	ORPHA:99886	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0200143	ORPHA:332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency	NOT	HP:6000344	ORPHA:332	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0005219	ORPHA:332	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0001889	ORPHA:332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0100502	ORPHA:332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0000726	ORPHA:332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0001328	ORPHA:332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0002160	ORPHA:332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0002719	ORPHA:332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0002912	ORPHA:332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0025406	ORPHA:332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0001510	ORPHA:332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0002315	ORPHA:332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0003401	ORPHA:332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0006827	ORPHA:332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0009830	ORPHA:332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:332	Congenital intrinsic factor deficiency		HP:0012120	ORPHA:332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0008357	ORPHA:331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0011884	ORPHA:331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0030657	ORPHA:331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0000978	ORPHA:331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0001342	ORPHA:331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0001933	ORPHA:331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0005261	ORPHA:331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0007420	ORPHA:331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0012233	ORPHA:331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0030140	ORPHA:331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0000132	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0000225	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0000421	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0001058	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0001934	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0004846	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0006298	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0011889	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0011891	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0030137	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0031364	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0040232	ORPHA:331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0200067	ORPHA:331	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0001399	ORPHA:331	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0002037	ORPHA:331	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331	Congenital factor XIII deficiency		HP:0012324	ORPHA:331	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0005184	ORPHA:101016	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0001279	ORPHA:101016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0001688	ORPHA:101016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0005135	ORPHA:101016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0001250	ORPHA:101016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0001645	ORPHA:101016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0001664	ORPHA:101016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0004308	ORPHA:101016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0012332	ORPHA:101016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0500018	ORPHA:101016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0001197	ORPHA:101016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome		HP:0002900	ORPHA:101016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101016	Romano-Ward syndrome	NOT	HP:0000365	ORPHA:101016	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0001249	ORPHA:370968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0003236	ORPHA:370968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0008947	ORPHA:370968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0030046	ORPHA:370968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0030099	ORPHA:370968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000252	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0001263	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0001270	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002120	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002828	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0003325	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0007015	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0008981	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0011968	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0030197	ORPHA:370968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000028	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000054	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000478	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000486	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000545	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000580	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0000707	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0001315	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0001320	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0001321	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002079	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002093	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002119	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002465	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002505	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002518	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002650	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002827	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0002878	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0003327	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0003549	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0003712	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0004637	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0007361	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0008443	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0010628	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0010864	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370968	Congenital muscular dystrophy with intellectual disability		HP:0040173	ORPHA:370968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0001279	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0001962	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0002094	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0002321	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0003546	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0005110	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0012378	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0100749	ORPHA:334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0001658	ORPHA:334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0001727	ORPHA:334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:334	Hereditary atrial fibrillation		HP:0001907	ORPHA:334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001369	ORPHA:333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001371	ORPHA:333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001386	ORPHA:333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001609	ORPHA:333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0007470	ORPHA:333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0012379	ORPHA:333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0000707	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0000708	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001249	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001263	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001508	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001615	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002086	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002829	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0003444	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0003640	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0008947	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0010729	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0011842	ORPHA:333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0000502	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0000608	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0000766	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0000939	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001155	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001250	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001257	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001336	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001433	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001612	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001618	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001760	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001954	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002093	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002098	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002207	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002300	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002376	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002788	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002815	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0003019	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0003202	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0004322	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0005483	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0006511	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0007957	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0009811	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0011968	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0012444	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0025392	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0025405	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0025423	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0100750	ORPHA:333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0000639	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001395	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001399	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001541	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001686	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001789	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001831	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001873	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001903	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0001999	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002028	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002385	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002716	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0002910	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0006575	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0007759	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0009381	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:333	Farber disease		HP:0012469	ORPHA:333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0002061	ORPHA:101010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0002064	ORPHA:101010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0002317	ORPHA:101010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0002395	ORPHA:101010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0003487	ORPHA:101010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0007020	ORPHA:101010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0008969	ORPHA:101010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0000570	ORPHA:101010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0001251	ORPHA:101010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0002936	ORPHA:101010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0003474	ORPHA:101010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0003693	ORPHA:101010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0007141	ORPHA:101010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0012407	ORPHA:101010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101010	Autosomal spastic paraplegia type 30		HP:0100275	ORPHA:101010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001250	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001320	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001385	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001629	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001999	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0002007	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0002015	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0002020	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0002033	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0002079	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0002119	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0002650	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0007018	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0007305	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0011229	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0012803	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0031910	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0100704	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0100716	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000478	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001249	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001252	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001263	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001511	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0001627	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0008897	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0011968	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0410263	ORPHA:494344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000028	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000047	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000076	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000119	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000286	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000347	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000365	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000358	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000453	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000463	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000483	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000486	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000508	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000545	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000565	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000567	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000568	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000577	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000581	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000612	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000648	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000659	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000708	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494344	RERE-related neurodevelopmental syndrome		HP:0000729	ORPHA:494344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0001260	ORPHA:101011	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0001285	ORPHA:101011	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0002015	ORPHA:101011	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0002483	ORPHA:101011	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0001348	ORPHA:101011	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0002064	ORPHA:101011	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0008994	ORPHA:101011	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0001276	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0001288	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0001761	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0001288	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0002395	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0002936	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0007350	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0008956	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0009046	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0010831	ORPHA:101011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101011	Autosomal dominant spastic paraplegia type 31		HP:0030237	ORPHA:101011	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0003645	ORPHA:330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0004841	ORPHA:330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0001907	ORPHA:330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0001977	ORPHA:330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0007985	ORPHA:330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0012636	ORPHA:330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0200067	ORPHA:330	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0001026	ORPHA:330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330	Congenital factor XII deficiency		HP:0001892	ORPHA:330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002897	ORPHA:99880	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0003072	ORPHA:99880	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0008200	ORPHA:99880	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002148	ORPHA:99880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002150	ORPHA:99880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0003165	ORPHA:99880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0011766	ORPHA:99880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0000121	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0000131	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0000787	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0000939	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0001959	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002015	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0003072	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0010614	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0012232	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0012378	ORPHA:99880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0000083	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0000107	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0000934	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0001324	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0001733	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002017	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002019	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002315	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002574	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002653	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0004398	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0008696	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0200025	ORPHA:99880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002667	ORPHA:99880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0002890	ORPHA:99880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0006725	ORPHA:99880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0010788	ORPHA:99880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99880	Hyperparathyroidism-jaw tumor syndrome		HP:0012032	ORPHA:99880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000276	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000316	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001166	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001252	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001548	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0010864	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0011220	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0011229	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0045075	ORPHA:457359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000218	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000256	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000303	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000358	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000400	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000494	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000520	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000582	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001263	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001344	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001355	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001519	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001520	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001533	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001833	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001999	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002066	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002069	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002307	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001288	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002751	ORPHA:457359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000054	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000272	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000297	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000325	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000426	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000472	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0000586	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0012760	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001321	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001334	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001376	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001382	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001555	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001763	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0001998	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002119	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002120	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002808	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0002938	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0006863	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0007074	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0007204	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0011003	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome		HP:0011330	ORPHA:457359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0011438	ORPHA:40366	TAS		HP:0040280			H	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000218	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000252	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000286	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000347	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000378	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000463	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000479	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000778	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0001622	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0001662	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0001710	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0001999	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0005104	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0006695	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0008058	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0008364	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0008551	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0008619	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0009099	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0009117	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0012759	ORPHA:40366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0000384	ORPHA:40366	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0001709	ORPHA:40366	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0006493	ORPHA:40366	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0006496	ORPHA:40366	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40366	Acitretin/etretinate embryopathy		HP:0009760	ORPHA:40366	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000252	ORPHA:457351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000407	ORPHA:457351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000505	ORPHA:457351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0001263	ORPHA:457351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002353	ORPHA:457351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000729	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000817	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0001250	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0001257	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0001344	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002069	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002121	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002123	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002342	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002540	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0006808	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0006863	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0008947	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0010864	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0011352	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0012443	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0100704	ORPHA:457351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000278	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000430	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0001319	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0001873	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002019	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002079	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002120	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002283	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002509	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002521	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002553	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002721	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0003189	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0005280	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0010838	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0011229	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0011290	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0011451	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0012444	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0012469	ORPHA:457351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0000733	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0001631	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002451	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0002650	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0004532	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0011471	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0020049	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457351	Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome		HP:0100716	ORPHA:457351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0001892	ORPHA:329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0001929	ORPHA:329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0003645	ORPHA:329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0006298	ORPHA:329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0010989	ORPHA:329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0000132	ORPHA:329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0000421	ORPHA:329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0002239	ORPHA:329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329	Congenital factor XI deficiency		HP:0005261	ORPHA:329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0010307	ORPHA:137935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0002098	ORPHA:137935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0011968	ORPHA:137935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0012735	ORPHA:137935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0030864	ORPHA:137935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0000329	ORPHA:137935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0000750	ORPHA:137935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0000961	ORPHA:137935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0001609	ORPHA:137935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0030828	ORPHA:137935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0002013	ORPHA:137935	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0002104	ORPHA:137935	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137935	Airway infantile hemangioma		HP:0002360	ORPHA:137935	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0000083	ORPHA:99879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0000121	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0000934	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0000938	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0002148	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0002150	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0002897	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0003072	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0003109	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0003165	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0008200	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0003072	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0011458	ORPHA:99879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99879	Familial isolated hyperparathyroidism		HP:0040160	ORPHA:99879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001627	ORPHA:97214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0002092	ORPHA:97214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0003546	ORPHA:97214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001324	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001962	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0002875	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0004755	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0005110	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0005115	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0005317	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0012378	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0012418	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0030148	ORPHA:97214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0000961	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001217	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001254	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001392	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001541	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001609	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001629	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001631	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001643	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001681	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001694	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001708	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001891	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0002098	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0002105	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0002240	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0003270	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0004756	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0004840	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0005180	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0006695	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0010741	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0011227	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0011604	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0011712	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0012382	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0012398	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0030848	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0030849	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0031138	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0100749	ORPHA:97214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0000083	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001279	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001297	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001636	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0001892	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0002149	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0002321	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0004308	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0005518	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0006689	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0007430	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0030049	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0030828	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97214	Eisenmenger syndrome		HP:0100724	ORPHA:97214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0008151	ORPHA:328	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0008321	ORPHA:328	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0004846	ORPHA:328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0006298	ORPHA:328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0000225	ORPHA:328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0000421	ORPHA:328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0000132	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0000790	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0000978	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0002239	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0005261	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0007420	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0011884	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0011891	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0012233	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0025328	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0030140	ORPHA:328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0002138	ORPHA:328	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:328	Congenital factor X deficiency		HP:0011854	ORPHA:328	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0003645	ORPHA:325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0008151	ORPHA:325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0040250	ORPHA:325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0000421	ORPHA:325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0001892	ORPHA:325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0002170	ORPHA:325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0005261	ORPHA:325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0000132	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0001903	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0002907	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0006298	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0011884	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0011890	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0011891	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0012233	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0012541	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0030137	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0030138	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency		HP:0030140	ORPHA:325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency	NOT	HP:0004420	ORPHA:325	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:325	Congenital factor II deficiency	NOT	HP:0004936	ORPHA:325	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000083	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000100	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000365	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000524	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000790	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000962	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000966	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001014	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001131	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001369	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001482	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001635	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001903	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002024	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002027	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002326	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002829	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0003326	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0004343	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0007957	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0012378	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0033595	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0034864	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0100579	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0100585	ORPHA:324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000091	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000093	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000112	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000179	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000280	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000360	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000518	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000648	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000708	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000823	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001646	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001653	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001678	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002017	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002039	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002046	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002097	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0003077	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0003119	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0003546	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0004322	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0011710	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0012532	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0031006	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0100543	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0500008	ORPHA:324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000407	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000716	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000739	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000822	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000873	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001004	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001250	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001297	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001637	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001639	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001681	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001712	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0001945	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002093	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002094	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002321	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002376	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002571	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0002823	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0004306	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0004349	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0006510	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0011675	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0100820	ORPHA:324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324	Fabry disease		HP:0000975	ORPHA:324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000003	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000278	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000337	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000343	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000486	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000494	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0001263	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0001770	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0002019	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0002514	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0004389	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0010956	ORPHA:73246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000028	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000252	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000369	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000411	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0000508	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0001166	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0001252	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0001511	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0001601	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0004279	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0006101	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0007678	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73246	Visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome		HP:0045075	ORPHA:73246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0002170	ORPHA:327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0002239	ORPHA:327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0000132	ORPHA:327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0000225	ORPHA:327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0000421	ORPHA:327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0000978	ORPHA:327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0004846	ORPHA:327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0005261	ORPHA:327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0008151	ORPHA:327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0000138	ORPHA:327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0010881	ORPHA:327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:327	Congenital factor VII deficiency		HP:0011891	ORPHA:327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73245	Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome		HP:0000518	ORPHA:73245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73245	Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome		HP:0001305	ORPHA:73245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73245	Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome		HP:0001320	ORPHA:73245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73245	Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome		HP:0002280	ORPHA:73245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73245	Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome		HP:0002460	ORPHA:73245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73245	Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome		HP:0003444	ORPHA:73245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73245	Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome		HP:0008944	ORPHA:73245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0000421	ORPHA:326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0005261	ORPHA:326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0000132	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0000225	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0000790	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0000978	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0001934	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0002239	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0004846	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0006298	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0007420	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0011890	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0011891	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0030137	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0030140	ORPHA:326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0002105	ORPHA:326	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0002170	ORPHA:326	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0002573	ORPHA:326	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:326	Congenital factor V deficiency		HP:0100608	ORPHA:326	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0001003	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0001045	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0001258	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0001347	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0002064	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0002515	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0002607	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0002751	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0012701	ORPHA:101003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0000085	ORPHA:101003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0001250	ORPHA:101003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0002218	ORPHA:101003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0002827	ORPHA:101003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101003	Autosomal recessive spastic paraplegia type 23		HP:0004322	ORPHA:101003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0030431	ORPHA:321	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0001376	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002763	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002815	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002823	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003330	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003959	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0004302	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0004322	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0012531	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0040069	ORPHA:321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0001369	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002673	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002857	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002991	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002992	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003016	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003026	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003326	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003474	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003977	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0005922	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0006385	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0006487	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0008800	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0009821	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0009826	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0010049	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0010501	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0025232	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0030883	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0032510	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0040071	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0100555	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0100559	ORPHA:321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0000016	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0000896	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0000918	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0001191	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0001850	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002015	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002107	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002144	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002176	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0002318	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003396	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0003406	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0004684	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0005214	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0006765	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0008443	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0012151	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0020110	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0031625	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0040163	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:321	Multiple osteochondromas		HP:0100749	ORPHA:321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000023	ORPHA:3191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000286	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000347	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000358	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000463	ORPHA:3191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000470	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000568	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000639	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0000691	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0001061	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0001080	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0001249	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0001513	ORPHA:3191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0001608	ORPHA:3191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0001682	ORPHA:3191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0002093	ORPHA:3191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0002650	ORPHA:3191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0002808	ORPHA:3191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0003119	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0004322	ORPHA:3191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0005048	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0005174	ORPHA:3191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0005978	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0007598	ORPHA:3191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0008777	ORPHA:3191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3191	Subaortic stenosis-short stature syndrome		HP:0011675	ORPHA:3191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001332	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001336	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001252	ORPHA:13	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002179	ORPHA:13	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0000508	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0000711	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0000713	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0000716	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0000750	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0000980	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001249	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001250	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001251	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001263	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001266	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001270	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001276	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0001347	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002015	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002063	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002067	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002071	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002072	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002169	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002329	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002421	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002487	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002521	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0002527	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0003781	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:13	6-pyruvoyl-tetrahydropterin synthase deficiency		HP:0010553	ORPHA:13	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101004	Autosomal recessive spastic paraplegia type 24		HP:0001257	ORPHA:101004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101004	Autosomal recessive spastic paraplegia type 24		HP:0001258	ORPHA:101004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101004	Autosomal recessive spastic paraplegia type 24		HP:0001347	ORPHA:101004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101004	Autosomal recessive spastic paraplegia type 24		HP:0002169	ORPHA:101004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101004	Autosomal recessive spastic paraplegia type 24		HP:0012407	ORPHA:101004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101004	Autosomal recessive spastic paraplegia type 24		HP:0030051	ORPHA:101004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101004	Autosomal recessive spastic paraplegia type 24		HP:0000407	ORPHA:101004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0000822	ORPHA:320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0002900	ORPHA:320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0003351	ORPHA:320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0000121	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0001508	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0001959	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0001960	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0004319	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0004322	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0011731	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0012603	ORPHA:320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0000083	ORPHA:320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0001095	ORPHA:320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0001297	ORPHA:320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0001511	ORPHA:320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess		HP:0001712	ORPHA:320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320	Apparent mineralocorticoid excess	NOT	HP:0012606	ORPHA:320	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000707	ORPHA:14	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001927	ORPHA:14	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002570	ORPHA:14	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002630	ORPHA:14	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0025201	ORPHA:14	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0100513	ORPHA:14	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000529	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000551	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000662	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001284	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001508	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001903	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001923	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002028	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002904	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003073	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003146	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003233	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003326	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003563	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0004905	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0007703	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0012153	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0100512	ORPHA:14	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000510	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000575	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000938	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001251	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001260	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001310	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001397	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001761	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001762	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002013	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002066	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002136	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002240	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002403	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002493	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002495	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002751	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002910	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003198	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003376	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0003487	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0006858	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0007894	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0008151	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0009053	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0010831	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0025022	ORPHA:14	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000508	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000602	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000618	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0000821	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001097	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001394	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001395	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001635	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001640	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0001892	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0002878	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:14	Abetalipoproteinemia		HP:0012804	ORPHA:14	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0002385	ORPHA:101005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0008441	ORPHA:101005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0000763	ORPHA:101005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0001258	ORPHA:101005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0012514	ORPHA:101005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0030833	ORPHA:101005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0000519	ORPHA:101005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0001087	ORPHA:101005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0003134	ORPHA:101005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0007141	ORPHA:101005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0008480	ORPHA:101005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0012513	ORPHA:101005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101005	Autosomal recessive spastic paraplegia type 25		HP:0100712	ORPHA:101005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3193	Supravalvular aortic stenosis		HP:0004381	ORPHA:3193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3193	Supravalvular aortic stenosis		HP:0011675	ORPHA:3193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3193	Supravalvular aortic stenosis		HP:0001279	ORPHA:3193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3193	Supravalvular aortic stenosis		HP:0001681	ORPHA:3193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3193	Supravalvular aortic stenosis		HP:0002094	ORPHA:3193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3193	Supravalvular aortic stenosis		HP:0031664	ORPHA:3193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3193	Supravalvular aortic stenosis		HP:0000822	ORPHA:3193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001249	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001288	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001324	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001347	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0002061	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0002120	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0003202	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0003487	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0007141	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0030890	ORPHA:101006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0000079	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0000518	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001317	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001332	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001761	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0002650	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0006938	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0007024	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0100660	ORPHA:101006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0001265	ORPHA:101006	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0008209	ORPHA:101006	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101006	Autosomal recessive spastic paraplegia type 26		HP:0040171	ORPHA:101006	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0002808	ORPHA:15	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0002979	ORPHA:15	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0003498	ORPHA:15	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0005619	ORPHA:15	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0009826	ORPHA:15	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000242	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000256	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000309	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000365	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000463	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0001156	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0001377	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0002007	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0002870	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0002938	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0003026	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0003194	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0003416	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0004060	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0005280	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0005819	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0008445	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0008947	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0010241	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0010536	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0011452	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0045086	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0045087	ORPHA:15	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000260	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000956	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0001513	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0002091	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0003180	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0003375	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0005257	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0008905	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0011867	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0012418	ORPHA:15	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:15	Achondroplasia		HP:0000238	ORPHA:15	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000039	ORPHA:322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000076	ORPHA:322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0002836	ORPHA:322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0004298	ORPHA:322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0010866	ORPHA:322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0100645	ORPHA:322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000020	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000023	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000048	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000075	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000077	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000083	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000085	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000089	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000136	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0001367	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0001539	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0004321	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0011024	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0011842	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0025489	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0030014	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0030261	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0040307	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0100599	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0100600	ORPHA:322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000028	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000069	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000110	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000238	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000252	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000271	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000290	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0000315	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0001627	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0002023	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0002025	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0002414	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0010475	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:322	Exstrophy-epispadias complex		HP:0012443	ORPHA:322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000246	ORPHA:73263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001945	ORPHA:73263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0012378	ORPHA:73263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0012531	ORPHA:73263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0012735	ORPHA:73263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0032162	ORPHA:73263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000572	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000622	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000629	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000819	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001291	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001622	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001742	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001875	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001993	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002013	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002014	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002018	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002027	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002105	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002107	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002113	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002202	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002248	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002315	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002383	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002583	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0004377	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0004387	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0005263	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0008066	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0011949	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0031417	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0032166	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0033661	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0032177	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0032564	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0032674	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0045026	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0100537	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0100539	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0100658	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0100721	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0100749	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0100750	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0200035	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0200039	ORPHA:73263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000083	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000123	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000265	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000421	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000508	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000520	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000541	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000544	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0000651	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001701	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0001733	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002239	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002249	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002573	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002586	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0002797	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0004418	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0004420	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0004944	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0007185	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0012115	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0012375	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0012819	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0020101	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0025059	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0025326	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0030049	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0031369	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73263	Zygomycosis		HP:0100584	ORPHA:73263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0000613	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0000670	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0000682	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0000982	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001072	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001131	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001156	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001817	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0003510	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0004279	ORPHA:3194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0000230	ORPHA:3194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001155	ORPHA:3194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001167	ORPHA:3194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001231	ORPHA:3194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0001622	ORPHA:3194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0005916	ORPHA:3194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0010783	ORPHA:3194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0000365	ORPHA:3194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0000662	ORPHA:3194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3194	Corneodermatoosseous syndrome		HP:0012047	ORPHA:3194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000316	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000750	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000924	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001155	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001257	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001260	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001263	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001270	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001290	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001317	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001328	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001347	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001350	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001382	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001510	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001760	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002015	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002019	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002313	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002464	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002495	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0003202	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0003484	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0003487	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0004322	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0005922	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0011094	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0012443	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0100518	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0100543	ORPHA:101000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000252	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000286	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000369	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000448	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000494	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000709	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000712	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000738	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000739	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001172	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001609	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0001761	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002064	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002360	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0002857	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0003693	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0005288	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0011098	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0011448	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0025269	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0030084	ORPHA:101000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101000	Autosomal recessive spastic paraplegia type 20		HP:0000126	ORPHA:101000	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000027	ORPHA:10	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000789	ORPHA:10	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000815	ORPHA:10	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001249	ORPHA:10	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001263	ORPHA:10	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002167	ORPHA:10	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0008734	ORPHA:10	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000098	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000179	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000286	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000316	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000389	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000486	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000581	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000582	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000670	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000679	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000682	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000684	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000716	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000739	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000771	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001252	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001337	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001513	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001763	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002019	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002099	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002205	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002974	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0003042	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0003043	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0004209	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0005469	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001382	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0007018	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0008872	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0010807	ORPHA:10	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000023	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000028	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000175	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000276	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000324	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000639	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000709	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000717	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0000733	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001250	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001251	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001260	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001385	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0001883	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002020	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002104	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002119	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002650	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0002665	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0005978	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0008736	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0012802	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:10	48,XXYY syndrome		HP:0030680	ORPHA:10	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3196	Steroid dehydrogenase deficiency-dental anomalies syndrome		HP:0000682	ORPHA:3196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3196	Steroid dehydrogenase deficiency-dental anomalies syndrome		HP:0001399	ORPHA:3196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3196	Steroid dehydrogenase deficiency-dental anomalies syndrome		HP:0006297	ORPHA:3196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3196	Steroid dehydrogenase deficiency-dental anomalies syndrome		HP:0011069	ORPHA:3196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0000726	ORPHA:101001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0001288	ORPHA:101001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0007256	ORPHA:101001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0001257	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0001263	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0001268	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0001288	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0001347	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0002015	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0002079	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0002186	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0002476	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0003134	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0006892	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0007340	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0010526	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0012075	ORPHA:101001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0001317	ORPHA:101001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101001	Autosomal recessive spastic paraplegia type 21		HP:0002071	ORPHA:101001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000252	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000316	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000358	ORPHA:11	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000431	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000486	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000582	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000823	ORPHA:11	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001249	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001252	ORPHA:11	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001263	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001357	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001385	ORPHA:11	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001643	ORPHA:11	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001671	ORPHA:11	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0001773	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0002974	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0004209	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0010978	ORPHA:11	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0100490	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0200055	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0000347	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:11	Pentasomy X syndrome		HP:0004322	ORPHA:11	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000490	ORPHA:444051	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0001263	ORPHA:444051	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000348	ORPHA:444051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0001511	ORPHA:444051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000316	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000322	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000365	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000478	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000598	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0000708	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0001252	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0001884	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0002007	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0002508	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0011800	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0012385	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0040019	ORPHA:444051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0001156	ORPHA:444051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444051	20q11.2 microdeletion syndrome		HP:0001181	ORPHA:444051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001251	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001257	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001276	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001336	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001347	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001387	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0002020	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0002036	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0002063	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0002380	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0003552	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0100022	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0100633	ORPHA:3197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001288	ORPHA:3197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001537	ORPHA:3197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0002360	ORPHA:3197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0100790	ORPHA:3197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001249	ORPHA:3197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001250	ORPHA:3197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0001373	ORPHA:3197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3197	Hereditary hyperekplexia		HP:0002827	ORPHA:3197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0007939	ORPHA:16	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0000545	ORPHA:16	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0000551	ORPHA:16	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0000639	ORPHA:16	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0025549	ORPHA:16	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0030619	ORPHA:16	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0000505	ORPHA:16	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0000512	ORPHA:16	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0000540	ORPHA:16	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0000613	ORPHA:16	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0001131	ORPHA:16	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:16	Blue cone monochromatism		HP:0007703	ORPHA:16	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0001258	ORPHA:101007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0002395	ORPHA:101007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0003487	ORPHA:101007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0005340	ORPHA:101007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0006938	ORPHA:101007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0001260	ORPHA:101007	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0002075	ORPHA:101007	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0007377	ORPHA:101007	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101007	Autosomal recessive spastic paraplegia type 27		HP:0000407	ORPHA:101007	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0001347	ORPHA:101008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0003487	ORPHA:101008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0001761	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0002061	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0002063	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0002064	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0002172	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0002317	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0002650	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0006944	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0007021	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0007340	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101008	Autosomal recessive spastic paraplegia type 28		HP:0010830	ORPHA:101008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0000399	ORPHA:87884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0000408	ORPHA:87884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0000750	ORPHA:87884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0001963	ORPHA:87884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0008596	ORPHA:87884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0011476	ORPHA:87884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0000405	ORPHA:87884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0005101	ORPHA:87884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0007670	ORPHA:87884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0011474	ORPHA:87884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0012713	ORPHA:87884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0012714	ORPHA:87884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87884	Non-syndromic genetic deafness		HP:0008573	ORPHA:87884	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002912	ORPHA:17	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0012120	ORPHA:17	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001263	ORPHA:17	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003535	ORPHA:17	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0008947	ORPHA:17	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0012379	ORPHA:17	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0012751	ORPHA:17	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001249	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001298	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001397	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001508	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001510	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002059	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002151	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002240	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002490	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002910	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003128	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003202	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0008347	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0011923	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0011924	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0011968	ORPHA:17	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000252	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000407	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000486	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000508	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000718	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000736	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000975	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001250	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001266	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001276	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001332	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001336	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001371	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001639	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001943	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002013	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002020	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002045	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002098	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002104	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002205	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002317	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002352	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002360	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0002487	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003200	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003201	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003557	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0012087	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0012240	ORPHA:17	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000047	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0000202	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001643	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001655	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0001680	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003097	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0003219	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0004742	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0005792	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0010442	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:17	Fatal infantile lactic acidosis with methylmalonic aciduria		HP:0011611	ORPHA:17	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0002395	ORPHA:101009	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0003487	ORPHA:101009	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0000365	ORPHA:101009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0001761	ORPHA:101009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0002036	ORPHA:101009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0002904	ORPHA:101009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0100790	ORPHA:101009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0002169	ORPHA:101009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0002495	ORPHA:101009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0007350	ORPHA:101009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0010936	ORPHA:101009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0001250	ORPHA:101009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0002034	ORPHA:101009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101009	Autosomal dominant spastic paraplegia type 29		HP:0010831	ORPHA:101009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0000121	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0001996	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002900	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0004349	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0004918	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0012405	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0032066	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0032944	ORPHA:18	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0000128	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0000787	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0001324	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0001508	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0001510	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002150	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0003109	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0004322	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0012608	ORPHA:18	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0000107	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0000114	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0000407	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0001944	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0001959	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002013	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002014	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002019	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002653	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002659	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002747	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002748	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0002749	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0003126	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0003355	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0004396	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0011387	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0011964	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0012213	ORPHA:18	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0001878	ORPHA:18	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:18	Distal renal tubular acidosis		HP:0003470	ORPHA:18	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000160	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000189	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000426	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000490	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000494	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000670	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000750	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0001249	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0001324	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0001328	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0001763	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0001845	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0002352	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0002553	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0002750	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0003458	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0004322	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0010761	ORPHA:457365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000179	ORPHA:457365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000331	ORPHA:457365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000508	ORPHA:457365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000592	ORPHA:457365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0000602	ORPHA:457365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457365	Intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome		HP:0001337	ORPHA:457365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002063	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002267	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0001288	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0003326	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0012894	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0030057	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0100543	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:5000002	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:5000007	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0000739	ORPHA:3198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0000975	ORPHA:3198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002527	ORPHA:3198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0003457	ORPHA:3198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0011964	ORPHA:3198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0000712	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0000756	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0001288	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0001336	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0001347	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002015	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002019	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:5000011	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:5000012	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:5000014	ORPHA:3198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0000651	ORPHA:3198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0000819	ORPHA:3198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0000821	ORPHA:3198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002104	ORPHA:3198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002321	ORPHA:3198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0002938	ORPHA:3198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder		HP:0031825	ORPHA:3198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3198	Stiff person spectrum disorder	NOT	HP:0012639	ORPHA:3198	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0003560	ORPHA:370980	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001270	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001272	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001290	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001319	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001349	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001771	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001288	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0002359	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0002500	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0003324	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0003326	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0003394	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0003458	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0003797	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0007126	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0008180	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0012548	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0030051	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0030099	ORPHA:370980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0000252	ORPHA:370980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0002350	ORPHA:370980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0002751	ORPHA:370980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0001302	ORPHA:370980	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0002119	ORPHA:370980	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability		HP:0002282	ORPHA:370980	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370980	Congenital muscular dystrophy without intellectual disability	NOT	HP:0001249	ORPHA:370980	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0001876	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0001882	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0001903	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0004828	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0005508	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0012133	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0025035	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0031020	ORPHA:318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:318	Acute erythroid leukemia		HP:0005528	ORPHA:318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0001824	ORPHA:99867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0031378	ORPHA:99867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0031409	ORPHA:99867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100749	ORPHA:99867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0001324	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0001609	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0001945	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0002094	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0002664	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0002721	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0002960	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0004313	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0012735	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0030166	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0030208	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0045026	ORPHA:99867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0000099	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0000707	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0001370	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0001909	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0001915	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0002725	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0003326	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0005560	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0007108	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0007378	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0012288	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0012410	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0012539	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0031041	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100031	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100279	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100324	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100526	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100527	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100614	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99867	Thymoma		HP:0100787	ORPHA:99867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000252	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000962	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000988	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000992	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001034	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001824	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0004322	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0008066	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0010783	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0012733	ORPHA:317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000501	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000518	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000819	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000958	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001595	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001596	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0005588	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0007400	ORPHA:317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000035	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000365	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0000411	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001156	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001182	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001249	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0001597	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0002230	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0007957	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0008069	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:317	Erythrokeratodermia variabilis		HP:0030680	ORPHA:317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0000969	ORPHA:99868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0000975	ORPHA:99868	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0001824	ORPHA:99868	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0002094	ORPHA:99868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0003473	ORPHA:99868	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0005345	ORPHA:99868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0006597	ORPHA:99868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0012378	ORPHA:99868	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0012735	ORPHA:99868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0100521	ORPHA:99868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0100540	ORPHA:99868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0100721	ORPHA:99868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99868	Thymic carcinoma		HP:0100749	ORPHA:99868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0000252	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0000682	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0000691	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0001251	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0001511	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0003355	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0004322	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0005978	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3199	Stimmler syndrome		HP:0010864	ORPHA:3199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314	Erythroderma desquamativum		HP:0001051	ORPHA:314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314	Erythroderma desquamativum		HP:0001508	ORPHA:314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314	Erythroderma desquamativum		HP:0002014	ORPHA:314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314	Erythroderma desquamativum		HP:0010978	ORPHA:314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000656	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000958	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000962	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000989	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0001019	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0001597	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0008064	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0008070	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0100679	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0100840	ORPHA:313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000232	ORPHA:313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0011039	ORPHA:313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000083	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000164	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0000389	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0001944	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0002205	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0004322	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0100543	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0100758	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313	Lamellar ichthyosis		HP:0100806	ORPHA:313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:316	Progressive symmetric erythrokeratodermia		HP:0000982	ORPHA:316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:316	Progressive symmetric erythrokeratodermia		HP:0010783	ORPHA:316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:316	Progressive symmetric erythrokeratodermia		HP:0200035	ORPHA:316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0001028	ORPHA:141184	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0007466	ORPHA:141184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0007618	ORPHA:141184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0031449	ORPHA:141184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0100585	ORPHA:141184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0001015	ORPHA:141184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0001635	ORPHA:141184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0001873	ORPHA:141184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0100784	ORPHA:141184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0410266	ORPHA:141184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0010885	ORPHA:141184	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0031207	ORPHA:141184	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma		HP:0100578	ORPHA:141184	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141184	Rapidly involuting congenital hemangioma	NOT	HP:0012329	ORPHA:141184	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000233	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000272	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000286	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000343	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000369	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000414	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001182	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001508	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001627	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0002194	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0002705	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0007687	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0009748	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0010862	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0012745	ORPHA:485405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000154	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000278	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000280	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000293	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000486	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000540	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000545	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000574	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000739	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000752	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0000824	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001156	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001212	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001511	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001631	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001649	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001702	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0001822	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0003196	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0004691	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0007018	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0008689	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0008947	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0009237	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0011040	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0012166	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0012170	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0012450	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485405	16p12.1p12.3 triplication syndrome		HP:0040025	ORPHA:485405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0000238	ORPHA:73256	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0010576	ORPHA:73256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0025354	ORPHA:73256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0030047	ORPHA:73256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0000504	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0000716	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0001251	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0002017	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0002315	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0002514	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0002516	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0008000	ORPHA:73256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0000360	ORPHA:73256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0001254	ORPHA:73256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0001259	ORPHA:73256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0002172	ORPHA:73256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0003401	ORPHA:73256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0003487	ORPHA:73256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73256	Central neurocytoma		HP:0007021	ORPHA:73256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:315	Erythrokeratoderma ''en cocardes''		HP:0000962	ORPHA:315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:315	Erythrokeratoderma ''en cocardes''		HP:0001000	ORPHA:315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:315	Erythrokeratoderma ''en cocardes''		HP:0008069	ORPHA:315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:315	Erythrokeratoderma ''en cocardes''		HP:0200034	ORPHA:315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:315	Erythrokeratoderma ''en cocardes''		HP:0002664	ORPHA:315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3180	Spondylocamptodactyly syndrome		HP:0000926	ORPHA:3180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3180	Spondylocamptodactyly syndrome		HP:0002650	ORPHA:3180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3180	Spondylocamptodactyly syndrome		HP:0100490	ORPHA:3180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0000819	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0001824	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002014	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002017	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002019	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002039	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002240	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002570	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002574	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002894	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0004396	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0004840	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0005609	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0012432	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0100833	ORPHA:97283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0001046	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0001406	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0001438	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0001541	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002239	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0005214	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0012334	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0030145	ORPHA:97283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0000820	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0000837	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0000845	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0000870	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0001031	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002865	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002893	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0002897	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0003072	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0003118	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0008200	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97283	Somatostatinoma		HP:0008256	ORPHA:97283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3181	Sprengel deformity		HP:0000175	ORPHA:3181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3181	Sprengel deformity		HP:0000470	ORPHA:3181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3181	Sprengel deformity		HP:0000473	ORPHA:3181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3181	Sprengel deformity		HP:0001435	ORPHA:3181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3181	Sprengel deformity		HP:0003043	ORPHA:3181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3181	Sprengel deformity		HP:0008952	ORPHA:3181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002894	ORPHA:97282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002900	ORPHA:97282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0005208	ORPHA:97282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0000819	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001824	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001895	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001944	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002017	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002024	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002039	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002240	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002574	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0003072	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0003324	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0003394	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0004396	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0010783	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0012432	ORPHA:97282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001046	ORPHA:97282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001406	ORPHA:97282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001438	ORPHA:97282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001541	ORPHA:97282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0012334	ORPHA:97282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0030895	ORPHA:97282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0000820	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0000837	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0000845	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0000870	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0001031	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002747	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002893	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002896	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0002897	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0003005	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0003118	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0003528	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0006719	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0006731	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0008200	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma		HP:0008256	ORPHA:97282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97282	VIPoma	NOT	HP:0002573	ORPHA:97282	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0030445	ORPHA:97287	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0001824	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002039	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002090	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002094	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002099	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002105	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002730	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0004396	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0006530	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0030828	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0031246	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0100749	ORPHA:97287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0000845	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0001005	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0001399	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0001708	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0001962	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002240	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0002615	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0003118	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0003144	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0003154	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0004385	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0005180	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0007380	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0012701	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:4000007	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0030149	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0030166	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97287	Bronchial neuroendocrine tumor		HP:0031566	ORPHA:97287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0000360	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0000365	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0001824	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0002015	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0002027	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0002239	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0002668	ORPHA:97286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0005214	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0006824	ORPHA:97286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97286	Carney-Stratakis syndrome		HP:0100723	ORPHA:97286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000252	ORPHA:3186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000356	ORPHA:3186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000413	ORPHA:3186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0001360	ORPHA:3186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0009927	ORPHA:3186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000202	ORPHA:3186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000568	ORPHA:3186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0002984	ORPHA:3186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0003022	ORPHA:3186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0003422	ORPHA:3186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0009601	ORPHA:3186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0011467	ORPHA:3186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000161	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000365	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000601	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000612	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0000921	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0001539	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0001636	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0001829	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0002269	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0002623	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0031095	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0008678	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0009829	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0009914	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3186	Holoprosencephaly-radial heart renal anomalies syndrome		HP:0100542	ORPHA:3186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0000853	ORPHA:97285	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0002665	ORPHA:97285	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0000475	ORPHA:97285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0000821	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0000872	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0001609	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0002015	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0002094	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0002716	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0002781	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0010307	ORPHA:97285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0000836	ORPHA:97285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0012531	ORPHA:97285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97285	Thyroid lymphoma		HP:0002098	ORPHA:97285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000158	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000160	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000179	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000256	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000280	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000286	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000311	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000316	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000347	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000358	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000365	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000444	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000483	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000486	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000494	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000508	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000574	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000577	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000629	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000646	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000684	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000718	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000722	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000750	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001263	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000805	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0000964	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001051	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001249	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001250	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001269	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001290	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001508	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001513	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001634	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001716	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001760	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0001763	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0002003	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0002019	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0002046	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0002079	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0002136	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0002705	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0003186	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0004209	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0006482	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0011246	ORPHA:369950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0012680	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369950	Intellectual disability-seizures-macrocephaly-obesity syndrome		HP:0100703	ORPHA:369950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0001347	ORPHA:171863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0002061	ORPHA:171863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0002064	ORPHA:171863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0002314	ORPHA:171863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0003487	ORPHA:171863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0006895	ORPHA:171863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0007020	ORPHA:171863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0002166	ORPHA:171863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0002169	ORPHA:171863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0007210	ORPHA:171863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0007340	ORPHA:171863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0100561	ORPHA:171863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42		HP:0001761	ORPHA:171863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42	NOT	HP:0001250	ORPHA:171863	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42	NOT	HP:0002921	ORPHA:171863	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42	NOT	HP:0003457	ORPHA:171863	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171863	Autosomal dominant spastic paraplegia type 42	NOT	HP:0012898	ORPHA:171863	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002894	ORPHA:97280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000206	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000819	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000988	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000989	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001824	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001895	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001927	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002014	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002017	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002019	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002039	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002240	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002574	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0004396	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0008066	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0010280	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0012432	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0031181	ORPHA:97280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000716	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001046	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001406	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001438	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001541	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001907	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002239	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002570	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0005214	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0012334	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0030145	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0030895	ORPHA:97280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000820	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000837	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000845	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0000870	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0001031	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002893	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0002897	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0003072	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0003118	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0008200	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97280	Glucagonoma		HP:0008256	ORPHA:97280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000286	ORPHA:90646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000316	ORPHA:90646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000381	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000405	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000408	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000708	ORPHA:90646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000815	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0000823	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0002750	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0001100	ORPHA:90646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0004452	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0100503	ORPHA:90646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0100543	ORPHA:90646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0007642	ORPHA:90646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0008669	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0011384	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0011388	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90646	Deafness-hypogonadism syndrome		HP:0012717	ORPHA:90646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0005184	ORPHA:90647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0008619	ORPHA:90647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0011476	ORPHA:90647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0001279	ORPHA:90647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0001664	ORPHA:90647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0007185	ORPHA:90647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0011675	ORPHA:90647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0030973	ORPHA:90647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0001250	ORPHA:90647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0001663	ORPHA:90647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90647	Jervell and Lange-Nielsen syndrome		HP:0001891	ORPHA:90647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3189	Congenital pulmonary valvar stenosis		HP:0001602	ORPHA:3189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3189	Congenital pulmonary valvar stenosis		HP:0001631	ORPHA:3189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3189	Congenital pulmonary valvar stenosis		HP:0030680	ORPHA:3189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0000364	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0000504	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0000708	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0000739	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0000825	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0000842	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0000975	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0001250	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0001254	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0001259	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0001337	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0001958	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0001962	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0001988	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0002044	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0002494	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0002591	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0003324	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0003401	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0004324	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0004372	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0006476	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0006767	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0007159	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0008200	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0008283	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0010534	ORPHA:97279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0010832	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0011446	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0012051	ORPHA:97279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0012378	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0100631	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0100634	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97279	Insulinoma		HP:0100785	ORPHA:97279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002894	ORPHA:97278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0100833	ORPHA:97278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0001438	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0001824	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002014	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002017	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002019	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002039	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002240	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002574	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0004396	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0030144	ORPHA:97278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0001046	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0001081	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0001406	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0001541	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002239	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0005214	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0006723	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0012334	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0030145	ORPHA:97278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0000820	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0000837	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0000845	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0000870	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0001031	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002893	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0002897	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0003072	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0003118	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0008200	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97278	PPoma		HP:0008256	ORPHA:97278	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0012418	ORPHA:330012	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0100598	ORPHA:330012	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002094	ORPHA:330012	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0000961	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0001649	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0001974	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002017	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002039	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002315	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002360	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0003546	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0012735	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0030830	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0031457	ORPHA:330012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0001945	ORPHA:330012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002321	ORPHA:330012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002789	ORPHA:330012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0012764	ORPHA:330012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0032016	ORPHA:330012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0100749	ORPHA:330012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330012	High altitude pulmonary edema		HP:0002105	ORPHA:330012	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000822	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002013	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002018	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002019	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002027	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002039	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0003270	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0012378	ORPHA:330015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000124	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000684	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000708	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000716	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000988	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001328	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001518	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001622	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001903	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002315	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002354	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002460	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002715	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002795	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0005268	ORPHA:330015	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0005560	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0007010	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0007015	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0007018	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0031058	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0032155	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0100511	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0100512	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0100543	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0100602	ORPHA:330015	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0100785	ORPHA:330015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000140	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0012760	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000789	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000798	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0000823	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001249	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001250	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001259	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001298	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0001970	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002099	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002270	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002750	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0002843	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0003141	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0003212	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0003233	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0003474	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0004437	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0005368	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0007178	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0009830	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0012207	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0012622	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0012864	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0030018	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0031429	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:330015	Lead poisoning		HP:0040306	ORPHA:330015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0001263	ORPHA:369942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0001396	ORPHA:369942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0000407	ORPHA:369942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0001250	ORPHA:369942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0001511	ORPHA:369942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0002500	ORPHA:369942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0030151	ORPHA:369942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0033643	ORPHA:369942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0000347	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0000486	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0000518	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0000835	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0001272	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0001332	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0002119	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0002910	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369942	CADDS		HP:0003196	ORPHA:369942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002119	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002126	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002169	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002350	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0006899	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0006955	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0012110	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0012695	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000541	ORPHA:370959	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000568	ORPHA:370959	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000618	ORPHA:370959	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001638	ORPHA:370959	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0003236	ORPHA:370959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0003560	ORPHA:370959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0030046	ORPHA:370959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0030099	ORPHA:370959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000158	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000238	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000252	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001263	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001317	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001321	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002198	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002282	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002363	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002365	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002938	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0003701	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0003707	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0003712	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0007204	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0007256	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0007260	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0012443	ORPHA:370959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000485	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000486	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000518	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000525	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000545	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000589	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000609	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0000648	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001250	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001256	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001274	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0001347	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement		HP:0002085	ORPHA:370959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000235	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000316	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000347	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000444	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000543	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0001250	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0002120	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0007370	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0100672	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000252	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000494	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0000518	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0001639	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0002353	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3173	Infantile spasms-broad thumbs syndrome		HP:0011304	ORPHA:3173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3175	X-linked spasticity-intellectual disability-epilepsy syndrome		HP:0001249	ORPHA:3175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3175	X-linked spasticity-intellectual disability-epilepsy syndrome		HP:0001257	ORPHA:3175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3175	X-linked spasticity-intellectual disability-epilepsy syndrome		HP:0001276	ORPHA:3175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3175	X-linked spasticity-intellectual disability-epilepsy syndrome		HP:0002063	ORPHA:3175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3175	X-linked spasticity-intellectual disability-epilepsy syndrome		HP:0002133	ORPHA:3175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3175	X-linked spasticity-intellectual disability-epilepsy syndrome		HP:0002301	ORPHA:3175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3175	X-linked spasticity-intellectual disability-epilepsy syndrome		HP:0003552	ORPHA:3175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0000848	ORPHA:171876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0001942	ORPHA:171876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0002153	ORPHA:171876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0002902	ORPHA:171876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0011740	ORPHA:171876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0040085	ORPHA:171876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0001531	ORPHA:171876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0001944	ORPHA:171876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0002013	ORPHA:171876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0031274	ORPHA:171876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0200117	ORPHA:171876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0001047	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0001081	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0001824	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0002754	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0003508	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0008872	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0011110	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0011675	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0012735	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0030828	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171876	Generalized pseudohypoaldosteronism type 1		HP:0200039	ORPHA:171876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0001007	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0001250	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0001518	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0001762	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0002205	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0002808	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0004322	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0005280	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0008780	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0010864	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0000518	ORPHA:85288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0001344	ORPHA:85288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0003144	ORPHA:85288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0000286	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0000486	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0000750	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85288	X-linked intellectual disability, Stocco Dos Santos type		HP:0000752	ORPHA:85288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0000736	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0000772	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0000826	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0000830	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0000863	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0001249	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0001273	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0001290	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0001328	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0002418	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0002474	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0003468	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0100710	ORPHA:280195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0000252	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0001355	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0001545	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0001680	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0002015	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0007330	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0007375	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0011471	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0012110	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0012650	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280195	Septopreoptic holoprosencephaly		HP:0031913	ORPHA:280195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85295	HSD10 disease, atypical type		HP:0000708	ORPHA:85295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85295	HSD10 disease, atypical type		HP:0001249	ORPHA:85295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85295	HSD10 disease, atypical type		HP:0100022	ORPHA:85295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85297	X-linked spinocerebellar ataxia type 3		HP:0000407	ORPHA:85297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85297	X-linked spinocerebellar ataxia type 3		HP:0000565	ORPHA:85297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85297	X-linked spinocerebellar ataxia type 3		HP:0000648	ORPHA:85297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85297	X-linked spinocerebellar ataxia type 3		HP:0001251	ORPHA:85297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85297	X-linked spinocerebellar ataxia type 3		HP:0001252	ORPHA:85297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85297	X-linked spinocerebellar ataxia type 3		HP:0001263	ORPHA:85297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85292	X-linked spinocerebellar ataxia type 4		HP:0002073	ORPHA:85292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85292	X-linked spinocerebellar ataxia type 4		HP:0000726	ORPHA:85292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85292	X-linked spinocerebellar ataxia type 4		HP:0001270	ORPHA:85292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85292	X-linked spinocerebellar ataxia type 4		HP:0002174	ORPHA:85292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85292	X-linked spinocerebellar ataxia type 4		HP:0002354	ORPHA:85292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85292	X-linked spinocerebellar ataxia type 4		HP:0001288	ORPHA:85292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85292	X-linked spinocerebellar ataxia type 4		HP:0007256	ORPHA:85292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000023	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000154	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000322	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000363	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000448	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000470	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000494	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000664	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000752	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001344	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002167	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002342	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0004209	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0004279	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0008736	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0010720	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0010807	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0010864	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0200021	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0200055	ORPHA:85293	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000179	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000218	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000256	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000581	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000718	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001337	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001513	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001761	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001773	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001852	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002136	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002650	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0004322	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0004326	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0008734	ORPHA:85293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000135	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000252	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000286	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000956	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0000975	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001250	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001770	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002353	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002721	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002808	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0002967	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0004422	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0001382	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85293	X-linked intellectual disability, Cabezas type		HP:0100490	ORPHA:85293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85294	X-linked epilepsy-learning disabilities-behavior disorders syndrome		HP:0000256	ORPHA:85294	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85294	X-linked epilepsy-learning disabilities-behavior disorders syndrome		HP:0000718	ORPHA:85294	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85294	X-linked epilepsy-learning disabilities-behavior disorders syndrome		HP:0001250	ORPHA:85294	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85294	X-linked epilepsy-learning disabilities-behavior disorders syndrome		HP:0001328	ORPHA:85294	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0005285	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0008905	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0011304	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0000303	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0000358	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0000358	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0000470	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0001156	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0001382	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0001552	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0001597	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0002938	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0003027	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0004482	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0011800	ORPHA:171866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0001609	ORPHA:171866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171866	Spondyloepimetaphyseal dysplasia, aggrecan type		HP:0002795	ORPHA:171866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3176	Spina bifida-hypospadias syndrome		HP:0000047	ORPHA:3176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3176	Spina bifida-hypospadias syndrome		HP:0002414	ORPHA:3176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3176	Spina bifida-hypospadias syndrome		HP:0010301	ORPHA:3176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0000505	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0001131	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0001251	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0002073	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0002342	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0002493	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0002503	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0007006	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3177	Spinocerebellar degeneration-corneal dystrophy syndrome		HP:0007957	ORPHA:3177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0000822	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0001250	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0001289	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0001332	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0001337	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0001649	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0001919	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002018	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002039	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002094	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002098	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002500	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002572	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002574	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002615	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002878	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0002900	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0003324	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0006515	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0007185	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330021	Mercury poisoning		HP:0100785	ORPHA:330021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0000154	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0000248	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0000303	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0000321	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0001250	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0001510	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0002300	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0002719	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0010814	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0010864	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0012471	ORPHA:85290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0000023	ORPHA:85290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0000034	ORPHA:85290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0000252	ORPHA:85290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0006956	ORPHA:85290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85290	X-linked intellectual disability, Wilson type		HP:0012448	ORPHA:85290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0000845	ORPHA:97261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0000280	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0001438	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0001824	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002014	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002017	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002019	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002039	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002044	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002240	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002574	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002894	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0003118	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0004396	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0007410	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0030144	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0100526	ORPHA:97261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0000820	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0000837	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0000870	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0001031	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0001046	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0001081	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0001406	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0001541	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002239	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002893	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002897	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0003072	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0005214	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0006723	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0008200	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0008256	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0012334	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0030145	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0100833	ORPHA:97261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0002666	ORPHA:97261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97261	GRFoma		HP:0100521	ORPHA:97261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0000252	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001249	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001250	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001263	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001272	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001290	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001508	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0011968	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0012345	ORPHA:370924	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0000028	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0000046	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0000054	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0000078	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0000648	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001511	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0001873	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370924	STT3B-CDG		HP:0002098	ORPHA:370924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0000958	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0000989	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0001019	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0002665	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0002716	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0002843	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0004332	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0008069	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0012192	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0100725	ORPHA:3162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0000982	ORPHA:3162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0001596	ORPHA:3162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0001744	ORPHA:3162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0002240	ORPHA:3162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0002721	ORPHA:3162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0008404	ORPHA:3162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0033221	ORPHA:3162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0000656	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0000969	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0001337	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0002045	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0002103	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0003202	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0007400	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0009830	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0010701	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0025143	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0025144	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3162	Sézary syndrome		HP:0100758	ORPHA:3162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0003256	ORPHA:370927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000252	ORPHA:370927	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001249	ORPHA:370927	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001263	ORPHA:370927	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001290	ORPHA:370927	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001999	ORPHA:370927	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000154	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000400	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000486	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000490	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000687	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001508	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0002013	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0002020	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0011024	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0011339	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0011968	ORPHA:370927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001250	ORPHA:370927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000085	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0000924	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001331	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001373	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001626	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001928	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0002079	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0002518	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0002650	ORPHA:370927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370927	SSR4-CDG		HP:0001643	ORPHA:370927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000023	ORPHA:3163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000407	ORPHA:3163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000490	ORPHA:3163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0003510	ORPHA:3163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0001382	ORPHA:3163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0007676	ORPHA:3163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000164	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000271	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000485	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000501	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000615	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000682	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000691	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000819	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000855	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0001596	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0001824	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0002167	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0004396	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0007392	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0008070	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0009125	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0011800	ORPHA:3163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000272	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000277	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000316	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000325	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000336	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000431	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000506	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000593	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0000627	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0001156	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0004279	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0007957	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0010668	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3163	SHORT syndrome		HP:0011220	ORPHA:3163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0000219	ORPHA:3164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0000465	ORPHA:3164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0000494	ORPHA:3164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0000499	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0000506	ORPHA:3164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0001252	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0001263	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0001539	ORPHA:3164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0001620	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0002000	ORPHA:3164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0002020	ORPHA:3164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0002023	ORPHA:3164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0002028	ORPHA:3164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0002643	ORPHA:3164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0002650	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0002714	ORPHA:3164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0005338	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0005956	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0008749	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0008872	ORPHA:3164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3164	Omphalocele syndrome, Shprintzen-Goldberg type		HP:0009555	ORPHA:3164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0000324	ORPHA:583097	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0000158	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0000293	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0000303	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0006288	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0007552	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0011801	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0012370	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0030812	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0430028	ORPHA:583097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0000995	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0001302	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0001572	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0002360	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0006349	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0007206	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0010535	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0012433	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0031023	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583097	Congenital infiltrating lipomatosis of the face		HP:0012478	ORPHA:583097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0000016	ORPHA:178475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0000508	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0000651	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0001260	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0001324	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0001695	ORPHA:178475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0001945	ORPHA:178475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0002015	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0002019	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0002094	ORPHA:178475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0002747	ORPHA:178475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0006597	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0006824	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0011499	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178475	Wound botulism		HP:0100021	ORPHA:178475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0000049	ORPHA:85277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0000322	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0000565	ORPHA:85277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0000729	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0000733	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0001249	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0001250	ORPHA:85277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0001319	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0001344	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0002020	ORPHA:85277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0002079	ORPHA:85277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0002119	ORPHA:85277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0002120	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0002273	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0003011	ORPHA:85277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0003196	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0010804	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85277	X-linked intellectual disability, Cantagrel type		HP:0011344	ORPHA:85277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0000217	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0000298	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0000389	ORPHA:178478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0000508	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0000600	ORPHA:178478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0000651	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0000822	ORPHA:178478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0001097	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0001252	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0001260	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0001284	ORPHA:178478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0001620	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0001695	ORPHA:178478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002015	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002019	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002027	ORPHA:178478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002039	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002094	ORPHA:178478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002307	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002360	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002607	ORPHA:178478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002615	ORPHA:178478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002747	ORPHA:178478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0002902	ORPHA:178478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0006824	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0011499	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0100021	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178478	Infant botulism		HP:0100022	ORPHA:178478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0005484	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0007370	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0008872	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0011968	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0100024	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000490	ORPHA:85278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000939	ORPHA:85278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002360	ORPHA:85278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002650	ORPHA:85278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0003199	ORPHA:85278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0001382	ORPHA:85278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0200134	ORPHA:85278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002300	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002307	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002353	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002487	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000275	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000276	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000400	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000486	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000574	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0001344	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002078	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002187	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002197	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002376	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002529	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0004326	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0011344	ORPHA:85278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000194	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000252	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000602	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000639	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000717	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000733	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000748	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000765	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0000767	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0001181	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0001250	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0001272	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0001508	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002015	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002019	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002020	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002066	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002119	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002120	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85278	Christianson syndrome		HP:0002194	ORPHA:85278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000028	ORPHA:85279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000327	ORPHA:85279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000750	ORPHA:85279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0002232	ORPHA:85279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0010864	ORPHA:85279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000718	ORPHA:85279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0001250	ORPHA:85279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0001257	ORPHA:85279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0001347	ORPHA:85279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0004322	ORPHA:85279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000218	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000252	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000256	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000411	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000426	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000486	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000490	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0000717	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0001182	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0001762	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0004279	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0007565	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0008734	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0030084	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85279	KDM5C-related syndromic X-linked intellectual disability		HP:0100490	ORPHA:85279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000028	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000076	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000089	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000110	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000175	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000238	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000252	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000365	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000369	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000411	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000444	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000568	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000609	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0000612	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0001162	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0001263	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0001357	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0001510	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0001511	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0001596	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0002251	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0002650	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0002937	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0003811	ORPHA:85284	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0005343	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0008064	ORPHA:85284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0008734	ORPHA:85284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0010864	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85284	BRESEK syndrome		HP:0012443	ORPHA:85284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000272	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000286	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000316	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000470	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000520	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000598	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000729	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000926	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000938	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001156	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001249	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001270	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001363	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001498	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001845	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002007	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001288	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002651	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002750	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002751	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002815	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0003196	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0003272	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0004322	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0004689	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0005280	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0010579	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0010804	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0012471	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0100864	ORPHA:457395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000164	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000252	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000369	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000766	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001256	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001290	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001763	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001838	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002812	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002857	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002944	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002967	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0003026	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0003100	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0003275	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0003307	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0003521	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0004209	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0004279	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0004568	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0005096	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0005639	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0006461	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0006863	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0010049	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0010585	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0012428	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0030292	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0030293	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0040261	ORPHA:457395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0000486	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001377	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001643	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001653	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001655	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001761	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0001863	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002079	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002342	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0002677	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0004592	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0008812	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457395	Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome		HP:0030427	ORPHA:457395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000028	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000047	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000054	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000089	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000104	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000233	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000238	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000239	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000248	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000262	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000272	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000316	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000337	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000343	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000347	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000348	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000369	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000463	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000581	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0000768	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001250	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001276	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001285	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001363	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001513	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001537	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001601	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001643	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0001770	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0002000	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0002059	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0002308	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0002342	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0002974	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0003196	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0004279	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0005280	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0006487	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0006610	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0007375	ORPHA:171839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171839	Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome		HP:0008551	ORPHA:171839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0000365	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0000544	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0001249	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0001257	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0001263	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0001266	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0001344	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0001531	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0002033	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0002421	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0004322	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0005484	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0008947	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0100660	ORPHA:85285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0000076	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0000126	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0000218	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0000446	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0000490	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0001347	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0002120	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0002987	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0003273	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0006380	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0006466	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85285	X-linked intellectual disability, Schimke type		HP:0011471	ORPHA:85285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000053	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000232	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000280	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000336	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000400	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000414	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000581	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0000750	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0001250	ORPHA:85286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0001513	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0002342	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85286	X-linked intellectual disability, Shashi type		HP:0100540	ORPHA:85286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0000028	ORPHA:85287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0000202	ORPHA:85287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0000204	ORPHA:85287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0000276	ORPHA:85287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0000455	ORPHA:85287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0000664	ORPHA:85287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0001176	ORPHA:85287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0001177	ORPHA:85287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0001256	ORPHA:85287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0002162	ORPHA:85287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0002650	ORPHA:85287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85287	X-linked intellectual disability, Siderius type		HP:0008734	ORPHA:85287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000218	ORPHA:85280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000252	ORPHA:85280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000272	ORPHA:85280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000322	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000490	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000494	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000767	ORPHA:85280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0000995	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0001182	ORPHA:85280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0001250	ORPHA:85280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0001956	ORPHA:85280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0001999	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0002342	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0002714	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0002967	ORPHA:85280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0004322	ORPHA:85280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85280	X-linked intellectual disability-cubitus valgus-dysmorphism syndrome		HP:0007598	ORPHA:85280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000028	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000054	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000252	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000293	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000311	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000340	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000639	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000713	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0000819	ORPHA:85282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001182	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001250	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001252	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001276	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001347	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001510	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001513	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0001762	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0002353	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0002714	ORPHA:85282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0003241	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0008736	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0009748	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0010864	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0011344	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85282	MEHMO syndrome		HP:0012471	ORPHA:85282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0000135	ORPHA:85283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0000324	ORPHA:85283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0000482	ORPHA:85283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0000577	ORPHA:85283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0001838	ORPHA:85283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0003202	ORPHA:85283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0001382	ORPHA:85283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0007477	ORPHA:85283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85283	X-linked intellectual disability, Miles-Carpenter type		HP:0010864	ORPHA:85283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0000969	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0001063	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0001369	ORPHA:3165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0001482	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0001824	ORPHA:3165	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0001879	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0001880	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0002829	ORPHA:3165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0003326	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0003401	ORPHA:3165	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0012378	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0012733	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0100537	ORPHA:3165	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0100614	ORPHA:3165	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0100658	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3165	Eosinophilic fasciitis		HP:0100748	ORPHA:3165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0040320	ORPHA:228302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0001324	ORPHA:228302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003455	ORPHA:228302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0045045	ORPHA:228302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0100295	ORPHA:228302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0000083	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0001970	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003201	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003236	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003394	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003449	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003710	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003774	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0008682	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0009058	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0011964	ORPHA:228302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0002913	ORPHA:228302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003326	ORPHA:228302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003546	ORPHA:228302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0003738	ORPHA:228302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228302	Carnitine palmitoyl transferase II deficiency, myopathic form		HP:0012380	ORPHA:228302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000219	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000280	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000286	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000316	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000319	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000369	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000431	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000629	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0000943	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001081	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001250	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001256	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001290	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001382	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001433	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001609	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001847	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001939	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001999	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002240	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002354	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002474	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002487	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002574	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002705	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002781	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0002910	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0003645	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0004691	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0007018	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0008151	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0008443	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0010535	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0011220	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0012103	ORPHA:3166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3166	Sialuria		HP:0001263	ORPHA:3166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0004923	ORPHA:238583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0000708	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0001252	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0003781	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0003785	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0012758	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0040206	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0040210	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0040416	ORPHA:238583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0000252	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0000750	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0001250	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0001276	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0001300	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0001332	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0002135	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0002360	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0002421	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0002917	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0004904	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0010553	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0033594	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:0100543	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238583	Hyperphenylalaninemia due to tetrahydrobiopterin deficiency		HP:6000482	ORPHA:238583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0008419	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0008818	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0009381	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0009832	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0009834	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0010052	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0011304	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0001156	ORPHA:3168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0001761	ORPHA:3168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0001840	ORPHA:3168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0002650	ORPHA:3168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0003180	ORPHA:3168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0005819	ORPHA:3168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0010239	ORPHA:3168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0012385	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0000286	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0000300	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0000926	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0001533	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0001597	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0001782	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0001783	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0003418	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0003468	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0004679	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3168	Sillence syndrome		HP:0006170	ORPHA:3168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0002910	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003201	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0006929	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0011675	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0012380	ORPHA:228305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001324	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0002315	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0002574	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0002913	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003198	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003236	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003326	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003449	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003546	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003710	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0003738	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0008315	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0011936	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0011964	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0040320	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0045045	ORPHA:228305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001250	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001305	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001397	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001399	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001638	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001714	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0001985	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		HP:0002240	ORPHA:228305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0000062	ORPHA:3169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0000079	ORPHA:3169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0002023	ORPHA:3169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0008678	ORPHA:3169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0010305	ORPHA:3169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0010497	ORPHA:3169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0001626	ORPHA:3169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0002414	ORPHA:3169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0002575	ORPHA:3169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3169	Sirenomelia		HP:0006501	ORPHA:3169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0000365	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0001394	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0001396	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0001397	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0001511	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0001994	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0003128	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0003281	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0012464	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0012465	ORPHA:53693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53693	GRACILE syndrome		HP:0100613	ORPHA:53693	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000252	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000343	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000664	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000885	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000894	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001027	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001061	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001373	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001382	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001510	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001763	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0002240	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0002342	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0002673	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0003015	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0003026	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0004322	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0005616	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0011304	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0012471	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0030084	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0100864	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0500011	ORPHA:370930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000175	ORPHA:370930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000520	ORPHA:370930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0000545	ORPHA:370930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001007	ORPHA:370930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0001956	ORPHA:370930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370930	XYLT1-CDG		HP:0004482	ORPHA:370930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002913	ORPHA:228308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0008315	ORPHA:228308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0011936	ORPHA:228308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0012380	ORPHA:228308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0040320	ORPHA:228308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0045045	ORPHA:228308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0000083	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0000113	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0000800	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001250	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001274	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001399	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001638	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001985	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002240	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002269	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002514	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002643	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0003077	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0003215	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0003236	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0011675	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0011968	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0012443	ORPHA:228308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0000238	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001259	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001290	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001302	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001320	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001397	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001637	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001640	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001942	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001970	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0001987	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002119	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002126	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002134	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0002705	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0006559	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0007229	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0008682	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		HP:0012722	ORPHA:228308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53697	Gnathodiaphyseal dysplasia		HP:0000935	ORPHA:53697	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53697	Gnathodiaphyseal dysplasia		HP:0000938	ORPHA:53697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53697	Gnathodiaphyseal dysplasia		HP:0002650	ORPHA:53697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53697	Gnathodiaphyseal dysplasia		HP:0002757	ORPHA:53697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53697	Gnathodiaphyseal dysplasia		HP:0006487	ORPHA:53697	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53697	Gnathodiaphyseal dysplasia		HP:0007626	ORPHA:53697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53697	Gnathodiaphyseal dysplasia		HP:0012802	ORPHA:53697	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000375	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000399	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000407	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000505	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000648	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000649	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000708	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0001268	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0001332	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0001751	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0002283	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0003487	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0004463	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0006801	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0007256	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0007325	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0007377	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0008596	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0011448	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0012048	ORPHA:52368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000551	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000572	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000603	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000613	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000726	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000751	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0000763	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0001337	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0002015	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0002172	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0002186	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0002340	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0002362	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0002540	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0004373	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0004432	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0009830	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0011951	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0011999	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0100704	ORPHA:52368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52368	Mohr-Tranebjaerg syndrome		HP:0007018	ORPHA:52368	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0001347	ORPHA:444099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0002061	ORPHA:444099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0002064	ORPHA:444099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0002314	ORPHA:444099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0003487	ORPHA:444099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0007020	ORPHA:444099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0000012	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0000020	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0002166	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0001288	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0003457	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0007199	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0008944	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0009053	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0012898	ORPHA:444099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73		HP:0001761	ORPHA:444099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73	NOT	HP:0000726	ORPHA:444099	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73	NOT	HP:0001250	ORPHA:444099	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:444099	Autosomal dominant spastic paraplegia type 73	NOT	HP:0002921	ORPHA:444099	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0000961	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001511	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001518	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001622	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001640	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001667	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0002240	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0002789	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0002878	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0004887	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0005180	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0010772	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0012418	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0031441	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0031443	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0031664	ORPHA:555874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001655	ORPHA:555874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001698	ORPHA:555874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0001704	ORPHA:555874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555874	Congenital tricuspid valve dysplasia		HP:0030718	ORPHA:555874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0000964	ORPHA:263534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0008064	ORPHA:263534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0008066	ORPHA:263534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0008499	ORPHA:263534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0010783	ORPHA:263534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0012393	ORPHA:263534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0040189	ORPHA:263534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0000953	ORPHA:263534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0007605	ORPHA:263534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0012733	ORPHA:263534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0200034	ORPHA:263534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263534	Acral peeling skin syndrome		HP:0200041	ORPHA:263534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0000648	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0000651	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0000763	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0001251	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0001288	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0001881	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0001928	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0002321	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0004374	ORPHA:3151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0007256	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0008064	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3151	Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome		HP:0100654	ORPHA:3151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0000098	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0000366	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0000407	ORPHA:3152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0000508	ORPHA:3152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0000648	ORPHA:3152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0001233	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0003103	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0004493	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0005019	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0006101	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0009838	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0010628	ORPHA:3152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0011001	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3152	Sclerosteosis		HP:0100798	ORPHA:3152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001653	ORPHA:555877	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0005180	ORPHA:555877	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0010444	ORPHA:555877	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001634	ORPHA:555877	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001659	ORPHA:555877	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0000189	ORPHA:555877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001382	ORPHA:555877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001647	ORPHA:555877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001763	ORPHA:555877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0031624	ORPHA:555877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0000179	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0000316	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0000343	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0000347	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0000767	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0000974	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001290	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001488	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0001643	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0002079	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0002094	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0002650	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0030718	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:555877	FLNA-related X-linked myxomatous valvular dysplasia		HP:0032388	ORPHA:555877	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0000962	ORPHA:171851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0001249	ORPHA:171851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0002242	ORPHA:171851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0008064	ORPHA:171851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0009830	ORPHA:171851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0001406	ORPHA:171851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0010837	ORPHA:171851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171851	MEDNIK syndrome		HP:0011967	ORPHA:171851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0000148	ORPHA:65681	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0000130	ORPHA:65681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0000786	ORPHA:65681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0002027	ORPHA:65681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0030011	ORPHA:65681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0031500	ORPHA:65681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0031501	ORPHA:65681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0003762	ORPHA:65681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0030160	ORPHA:65681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0100674	ORPHA:65681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0000145	ORPHA:65681	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:65681	Vaginal atresia		HP:0000813	ORPHA:65681	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0000365	ORPHA:65682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0000952	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0000989	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0001081	ORPHA:65682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0001394	ORPHA:65682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0001402	ORPHA:65682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0001733	ORPHA:65682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0001824	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0002017	ORPHA:65682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0002027	ORPHA:65682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0002028	ORPHA:65682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0002039	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0002611	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0002910	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0011985	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65682	Benign recurrent intrahepatic cholestasis		HP:0012378	ORPHA:65682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0000707	ORPHA:65683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0001250	ORPHA:65683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0002361	ORPHA:65683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0012757	ORPHA:65683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0410263	ORPHA:65683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0000708	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0001256	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0001269	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0002384	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0002536	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0006891	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0007359	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0030890	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0031951	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0100543	ORPHA:65683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0002197	ORPHA:65683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0007334	ORPHA:65683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0010864	ORPHA:65683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0011097	ORPHA:65683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0012469	ORPHA:65683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65683	Isolated focal cortical dysplasia		HP:0025170	ORPHA:65683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0001324	ORPHA:65684	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0001337	ORPHA:65684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0002380	ORPHA:65684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0002398	ORPHA:65684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0002715	ORPHA:65684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0002817	ORPHA:65684	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0003134	ORPHA:65684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0003457	ORPHA:65684	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0007149	ORPHA:65684	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65684	Monomelic amyotrophy		HP:0100022	ORPHA:65684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0000508	ORPHA:178487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0000651	ORPHA:178487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0001324	ORPHA:178487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0002014	ORPHA:178487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0002094	ORPHA:178487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0002747	ORPHA:178487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0006597	ORPHA:178487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0006824	ORPHA:178487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178487	Adult intestinal botulism		HP:0100021	ORPHA:178487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0000175	ORPHA:85273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0000252	ORPHA:85273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0000340	ORPHA:85273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0000365	ORPHA:85273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0000411	ORPHA:85273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0000426	ORPHA:85273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0000767	ORPHA:85273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0001249	ORPHA:85273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0002650	ORPHA:85273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0004322	ORPHA:85273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0008734	ORPHA:85273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85273	X-linked intellectual disability, Abidi type		HP:0100335	ORPHA:85273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0000028	ORPHA:85274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0000054	ORPHA:85274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0000135	ORPHA:85274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0000572	ORPHA:85274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0000692	ORPHA:85274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0001182	ORPHA:85274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0001249	ORPHA:85274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0001324	ORPHA:85274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0001513	ORPHA:85274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0002231	ORPHA:85274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0002342	ORPHA:85274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0002546	ORPHA:85274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0004322	ORPHA:85274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0006482	ORPHA:85274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85274	Syndromic X-linked intellectual disability 7		HP:0008736	ORPHA:85274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85275	Microphthalmia-ankyloblepharon-intellectual disability syndrome		HP:0000528	ORPHA:85275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85275	Microphthalmia-ankyloblepharon-intellectual disability syndrome		HP:0000568	ORPHA:85275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85275	Microphthalmia-ankyloblepharon-intellectual disability syndrome		HP:0001256	ORPHA:85275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85275	Microphthalmia-ankyloblepharon-intellectual disability syndrome		HP:0009755	ORPHA:85275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000023	ORPHA:85276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000028	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000154	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000175	ORPHA:85276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000248	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000256	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000286	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000303	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000322	ORPHA:85276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000337	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000347	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000400	ORPHA:85276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000486	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000494	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000501	ORPHA:85276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000518	ORPHA:85276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0000996	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0001250	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0001263	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0001377	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0001643	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0001671	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0001773	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0001992	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0002120	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0002342	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0002714	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0003355	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0004322	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0005280	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0005306	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0007413	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0009811	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0010864	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0011800	ORPHA:85276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0012023	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0200055	ORPHA:85276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85276	X-linked intellectual disability, Armfield type		HP:0400004	ORPHA:85276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0000217	ORPHA:178481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0000508	ORPHA:178481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0000651	ORPHA:178481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0001252	ORPHA:178481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0001260	ORPHA:178481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0001522	ORPHA:178481	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0002014	ORPHA:178481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0002015	ORPHA:178481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0002017	ORPHA:178481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0002094	ORPHA:178481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0002747	ORPHA:178481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0006824	ORPHA:178481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178481	Intestinal botulism		HP:0011499	ORPHA:178481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0000572	ORPHA:171844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0000618	ORPHA:171844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0001166	ORPHA:171844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0002650	ORPHA:171844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0000486	ORPHA:171844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0000518	ORPHA:171844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0000541	ORPHA:171844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0000565	ORPHA:171844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0001132	ORPHA:171844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0007703	ORPHA:171844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171844	Blindness-scoliosis-arachnodactyly syndrome		HP:0012376	ORPHA:171844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0000823	ORPHA:314811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0002750	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0001510	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0004322	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0001943	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0001946	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0002013	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0002027	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0004323	ORPHA:314811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0004325	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314811	Short stature due to GHSR deficiency		HP:0030353	ORPHA:314811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0000090	ORPHA:3156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0000505	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0000518	ORPHA:3156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0000529	ORPHA:3156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0000556	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0000822	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0001251	ORPHA:3156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0001263	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0002612	ORPHA:3156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0003774	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0004322	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0004348	ORPHA:3156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0007703	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0008209	ORPHA:3156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0010579	ORPHA:3156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3156	Senior-Loken syndrome		HP:0012622	ORPHA:3156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000505	ORPHA:3157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000609	ORPHA:3157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0100842	ORPHA:3157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000028	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000175	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000486	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000639	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000864	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0001250	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0001274	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0001331	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0004322	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0004374	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0008736	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0010627	ORPHA:3157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000407	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000458	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000717	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000873	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000958	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0000966	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0001249	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0001263	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0001513	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0001959	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0002019	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0002032	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0002360	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0002575	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0007360	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0009800	ORPHA:3157	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0012378	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3157	Septo-optic dysplasia spectrum		HP:0030680	ORPHA:3157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0000729	ORPHA:370943	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0001256	ORPHA:370943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0004976	ORPHA:370943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0001385	ORPHA:370943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0001765	ORPHA:370943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0002121	ORPHA:370943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0002342	ORPHA:370943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0002650	ORPHA:370943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0002827	ORPHA:370943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370943	Autism spectrum disorder-epilepsy-arthrogryposis syndrome		HP:0010864	ORPHA:370943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001892	ORPHA:71493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001894	ORPHA:71493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0004420	ORPHA:71493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0004936	ORPHA:71493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0000975	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0000989	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001744	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0002315	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0002326	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0002637	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0003401	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0004950	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0100749	ORPHA:71493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001123	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001250	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001260	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001279	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0001824	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0002092	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0002321	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0002863	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0004808	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0005268	ORPHA:71493	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:71493	Familial thrombocytosis		HP:0005506	ORPHA:71493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001880	ORPHA:3260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0000980	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001903	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001945	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001974	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002098	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002863	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0003270	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0031323	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0100724	ORPHA:3260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0000622	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0000708	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0000726	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0000964	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0000965	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0000989	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001019	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001025	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001217	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001250	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001289	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001298	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001324	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001347	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001369	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001386	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001433	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001508	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001635	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001644	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001727	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001733	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001744	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001785	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001873	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0001894	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002013	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002015	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002024	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002027	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002028	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002094	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002099	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002113	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002170	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002202	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002204	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002206	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002326	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002354	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002583	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002829	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0002910	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0003202	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0003326	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0003401	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0003474	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0004302	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0005115	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0005547	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0006253	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0006580	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0008872	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0008940	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0009830	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0011123	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0011897	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0011974	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0012735	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0025289	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0030151	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0030880	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0100665	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0100749	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0200029	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0200034	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0200036	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3260	Idiopathic hypereosinophilic syndrome		HP:0200123	ORPHA:3260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002960	ORPHA:3261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0000978	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001890	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001892	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001904	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001971	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001973	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002240	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002851	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0003237	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0005404	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0010702	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0011117	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0030886	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0033199	ORPHA:3261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001744	ORPHA:3261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002716	ORPHA:3261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002730	ORPHA:3261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0000099	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001025	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001880	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001888	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001923	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002633	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002848	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002850	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002923	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0003212	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0003261	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0003453	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0003493	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0003613	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0004315	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0004844	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0032218	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0012115	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0012189	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0012190	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0012191	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0012539	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0030080	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0031392	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0031393	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0034447	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0040126	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0100646	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0100827	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:6000016	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:6000017	ORPHA:3261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0000083	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0000554	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0000854	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001250	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001369	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001402	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0001789	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002113	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002206	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002315	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002583	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002671	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002725	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0002890	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0005263	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0005528	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0008069	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0008209	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0010619	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0011107	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0012490	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0031020	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3261	Autoimmune lymphoproliferative syndrome		HP:0100648	ORPHA:3261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0000160	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0000238	ORPHA:83473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0000256	ORPHA:83473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0000316	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0000348	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0000506	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0001162	ORPHA:83473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0001250	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0001355	ORPHA:83473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0001629	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0001653	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0001671	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0002126	ORPHA:83473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0005105	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0005280	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83473	Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome		HP:0100542	ORPHA:83473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217622	Sensorineural deafness with dilated cardiomyopathy		HP:0000365	ORPHA:217622	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217622	Sensorineural deafness with dilated cardiomyopathy		HP:0001635	ORPHA:217622	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217622	Sensorineural deafness with dilated cardiomyopathy		HP:0001644	ORPHA:217622	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217622	Sensorineural deafness with dilated cardiomyopathy		HP:0030872	ORPHA:217622	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217622	Sensorineural deafness with dilated cardiomyopathy		HP:0000403	ORPHA:217622	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0000175	ORPHA:63862	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0001518	ORPHA:63862	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0001539	ORPHA:63862	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0001622	ORPHA:63862	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0002323	ORPHA:63862	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0100333	ORPHA:63862	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0000776	ORPHA:63862	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0002084	ORPHA:63862	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0002414	ORPHA:63862	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0000104	ORPHA:63862	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0000252	ORPHA:63862	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0002023	ORPHA:63862	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0002575	ORPHA:63862	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0002983	ORPHA:63862	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63862	Schisis association		HP:0030680	ORPHA:63862	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0000988	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0001063	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0001873	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0001977	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0002958	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0003645	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0004855	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0005521	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0005543	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0008066	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0008151	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0011227	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0011900	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0012733	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0025022	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0025475	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0031273	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0031365	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0100758	ORPHA:49566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0001399	ORPHA:49566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0002170	ORPHA:49566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0002664	ORPHA:49566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0011029	ORPHA:49566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0100806	ORPHA:49566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49566	Acquired purpura fulminans		HP:0025452	ORPHA:49566	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:57196	Medial condensing osteitis of the clavicle		HP:0000889	ORPHA:57196	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57196	Medial condensing osteitis of the clavicle		HP:0010657	ORPHA:57196	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57196	Medial condensing osteitis of the clavicle		HP:0030834	ORPHA:57196	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57196	Medial condensing osteitis of the clavicle		HP:0006467	ORPHA:57196	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57196	Medial condensing osteitis of the clavicle		HP:0011227	ORPHA:57196	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0000836	ORPHA:99819	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0011790	ORPHA:99819	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0012188	ORPHA:99819	TAS		HP:0040280			H	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0000853	ORPHA:99819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0001824	ORPHA:99819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0002014	ORPHA:99819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0002378	ORPHA:99819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0008249	ORPHA:99819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0011784	ORPHA:99819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0000713	ORPHA:99819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0000752	ORPHA:99819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0001270	ORPHA:99819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0002360	ORPHA:99819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism		HP:0000520	ORPHA:99819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99819	Familial gestational hyperthyroidism	NOT	HP:0030057	ORPHA:99819	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000028	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000233	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000248	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000252	ORPHA:99812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000286	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000294	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000320	ORPHA:99812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000347	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000431	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000506	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000582	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000821	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000924	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000992	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0001249	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0001263	ORPHA:99812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0001510	ORPHA:99812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0001876	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0001974	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0002024	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0002240	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0002488	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0002665	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0002716	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0002721	ORPHA:99812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0003220	ORPHA:99812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0000444	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0004209	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0004422	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0004430	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0005561	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0005978	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0008736	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0010783	ORPHA:99812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99812	LIG4 syndrome		HP:0100585	ORPHA:99812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0000252	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0000567	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0000612	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0001376	ORPHA:3265	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0002435	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0003019	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0003042	ORPHA:3265	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0003070	ORPHA:3265	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0008056	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0008368	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3265	Isolated humero-radial synostosis		HP:0009601	ORPHA:3265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0000640	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0001251	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0001284	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0001761	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0002166	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0002283	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0002464	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0002503	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0003073	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0003124	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0003376	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0003693	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0006855	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0006858	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0007021	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0007141	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0009053	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0009830	ORPHA:94124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1		HP:0001250	ORPHA:94124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94124	Spinocerebellar ataxia with axonal neuropathy type 1	NOT	HP:0001249	ORPHA:94124	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0002910	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0003326	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0012384	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0012735	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0025426	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0025439	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0031464	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0100792	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0200042	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0200097	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0200136	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000036	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000217	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000491	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000572	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000613	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000716	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000790	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001010	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001128	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001600	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001875	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001919	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0002014	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0002090	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0003270	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0004378	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0004386	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0004887	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0008404	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0008682	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0010285	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0011354	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0012122	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0012375	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0012594	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0025416	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0030943	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0031088	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0031731	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0100518	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0200020	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0430007	ORPHA:95455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000618	ORPHA:95455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001798	ORPHA:95455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0006528	ORPHA:95455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0031368	ORPHA:95455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0100806	ORPHA:95455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001945	ORPHA:95455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0008066	ORPHA:95455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0011123	ORPHA:95455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0012378	ORPHA:95455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0030953	ORPHA:95455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000509	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000600	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000739	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000953	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000987	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0000988	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001097	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0001903	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0002039	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0002098	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95455	Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum		HP:0002315	ORPHA:95455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0000069	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0001048	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0001172	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0002974	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0003070	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0005916	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0009601	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0010935	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3266	Isolated humero-radio-ulnar synostosis		HP:0100560	ORPHA:3266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0000763	ORPHA:36258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0002633	ORPHA:36258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0004420	ORPHA:36258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0100758	ORPHA:36258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0200042	ORPHA:36258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0001063	ORPHA:36258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0002829	ORPHA:36258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0003401	ORPHA:36258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0004417	ORPHA:36258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0030880	ORPHA:36258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0033402	ORPHA:36258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0033505	ORPHA:36258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0000975	ORPHA:36258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0002638	ORPHA:36258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0031006	ORPHA:36258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0100785	ORPHA:36258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36258	Buerger disease		HP:0025324	ORPHA:36258	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0002470	ORPHA:94122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0000639	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0001260	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0001263	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0001290	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0001321	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0002066	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0002078	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0002080	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type		HP:0002136	ORPHA:94122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94122	Cerebellar ataxia, Cayman type	NOT	HP:0000479	ORPHA:94122	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000164	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000252	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000286	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000288	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000574	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000664	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000768	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0000772	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0001249	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0001263	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0001622	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0002650	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0002750	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0002974	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0004209	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0004322	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0006101	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0007477	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3268	Radioulnar synostosis-microcephaly-scoliosis syndrome		HP:0009811	ORPHA:3268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis		HP:0010446	ORPHA:95459	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis		HP:0030148	ORPHA:95459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis		HP:0005180	ORPHA:95459	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis		HP:0001635	ORPHA:95459	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis		HP:0002092	ORPHA:95459	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis		HP:0002615	ORPHA:95459	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis	NOT	HP:0001370	ORPHA:95459	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis	NOT	HP:0006689	ORPHA:95459	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:95459	Congenital tricuspid stenosis	NOT	HP:0100570	ORPHA:95459	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0002818	ORPHA:3269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0002974	ORPHA:3269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0002996	ORPHA:3269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0006394	ORPHA:3269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0040071	ORPHA:3269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0001457	ORPHA:3269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0003083	ORPHA:3269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0030834	ORPHA:3269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0030836	ORPHA:3269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0001159	ORPHA:3269	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0001374	ORPHA:3269	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0001762	ORPHA:3269	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3269	Isolated radio-ulnar synostosis		HP:0010442	ORPHA:3269	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0000602	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0000708	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0000872	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0001250	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0001251	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0001284	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0001288	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0001290	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0001310	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0002015	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0002315	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0002403	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0002406	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0002495	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0003390	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0003542	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0009830	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0012079	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0012251	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0100022	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0100543	ORPHA:94125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94125	Recessive mitochondrial ataxia syndrome		HP:0001260	ORPHA:94125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0002027	ORPHA:51890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0003474	ORPHA:51890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0010830	ORPHA:51890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0000975	ORPHA:51890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0002321	ORPHA:51890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0001974	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0002018	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0002039	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0003270	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0003418	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0003565	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0012533	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0100963	ORPHA:51890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0000010	ORPHA:51890	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0000023	ORPHA:51890	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0004325	ORPHA:51890	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51890	Anterior cutaneous nerve entrapment syndrome		HP:0004798	ORPHA:51890	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0000174	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0001290	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0001371	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0002808	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0003236	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0003306	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0003324	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0003458	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0003557	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0004303	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0005072	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0006149	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0100297	ORPHA:75840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0000347	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0000470	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0000473	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0000565	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0001181	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0001238	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0001324	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0001558	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0002359	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0002650	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0002827	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0002878	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0002987	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0003700	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0006380	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0008081	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0009113	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75840	Ullrich congenital muscular dystrophy		HP:0010511	ORPHA:75840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99811	Neuronal intestinal pseudoobstruction		HP:0000695	ORPHA:99811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99811	Neuronal intestinal pseudoobstruction		HP:0001643	ORPHA:99811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99811	Neuronal intestinal pseudoobstruction		HP:0002024	ORPHA:99811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99811	Neuronal intestinal pseudoobstruction		HP:0002719	ORPHA:99811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99811	Neuronal intestinal pseudoobstruction		HP:0004313	ORPHA:99811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99811	Neuronal intestinal pseudoobstruction		HP:0000776	ORPHA:99811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99811	Neuronal intestinal pseudoobstruction		HP:0001671	ORPHA:99811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0001249	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0001260	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0001336	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0002376	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0007221	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0007272	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0011166	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0011188	ORPHA:263516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0000252	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0000504	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0000648	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0000726	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0001272	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0001327	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0002059	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0002069	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0002073	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0002373	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0007370	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0011185	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0012462	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263516	Progressive myoclonic epilepsy type 3		HP:0045084	ORPHA:263516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000252	ORPHA:447980	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000750	ORPHA:447980	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001263	ORPHA:447980	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001511	ORPHA:447980	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001999	ORPHA:447980	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000160	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000276	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000286	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000322	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000347	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000369	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000448	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000506	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000545	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001270	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001344	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001510	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002342	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0012471	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0100807	ORPHA:447980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000175	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000340	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000358	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000430	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000494	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000540	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000582	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000646	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000666	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000737	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000752	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000826	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0000939	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001385	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001629	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0001761	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002019	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002020	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002059	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002092	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002373	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002572	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002751	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0002827	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0003186	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0008551	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0010864	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0012741	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0030043	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0030084	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447980	19p13.3 microduplication syndrome		HP:0100716	ORPHA:447980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238578	Familial clubfoot due to 17q23.1q23.2 microduplication		HP:0001385	ORPHA:238578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238578	Familial clubfoot due to 17q23.1q23.2 microduplication		HP:0001762	ORPHA:238578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238578	Familial clubfoot due to 17q23.1q23.2 microduplication		HP:0001800	ORPHA:238578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238578	Familial clubfoot due to 17q23.1q23.2 microduplication		HP:0004322	ORPHA:238578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0005048	ORPHA:3250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0008368	ORPHA:3250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0100264	ORPHA:3250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0100490	ORPHA:3250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0000407	ORPHA:3250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0001156	ORPHA:3250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0003042	ORPHA:3250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0003070	ORPHA:3250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0005880	ORPHA:3250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0005916	ORPHA:3250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0040019	ORPHA:3250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0000486	ORPHA:3250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0003019	ORPHA:3250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0004209	ORPHA:3250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3250	Proximal symphalangism		HP:0006101	ORPHA:3250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83465	Narcolepsy type 2		HP:0000708	ORPHA:83465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83465	Narcolepsy type 2		HP:0000738	ORPHA:83465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83465	Narcolepsy type 2		HP:0001262	ORPHA:83465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83465	Narcolepsy type 2		HP:0002360	ORPHA:83465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83465	Narcolepsy type 2		HP:0100785	ORPHA:83465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0008551	ORPHA:83463	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0040119	ORPHA:83463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0000377	ORPHA:83463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0000413	ORPHA:83463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0000750	ORPHA:83463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0008589	ORPHA:83463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0009892	ORPHA:83463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0001360	ORPHA:83463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83463	Microtia		HP:0007018	ORPHA:83463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0001541	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0001824	ORPHA:83469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0001903	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0002017	ORPHA:83469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0002027	ORPHA:83469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0002240	ORPHA:83469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0002585	ORPHA:83469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0002595	ORPHA:83469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0002716	ORPHA:83469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0002894	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0003270	ORPHA:83469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0004326	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0010788	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0100006	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0100242	ORPHA:83469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0100526	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0100615	ORPHA:83469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83469	Desmoplastic small round cell tumor		HP:0100721	ORPHA:83469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0012064	ORPHA:83468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0002653	ORPHA:83468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0002756	ORPHA:83468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0003926	ORPHA:83468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0006431	ORPHA:83468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0100253	ORPHA:83468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0002992	ORPHA:83468	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0012428	ORPHA:83468	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0000707	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0002143	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0002696	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0002867	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0003172	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0003312	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0003418	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0003979	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83468	Solitary bone cyst		HP:0100748	ORPHA:83468	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83467	Morvan syndrome		HP:5000005	ORPHA:83467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0000083	ORPHA:83472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0000100	ORPHA:83472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0001250	ORPHA:83472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0001257	ORPHA:83472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0001260	ORPHA:83472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0012444	ORPHA:83472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0000252	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0000648	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0000951	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0001249	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0001251	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0001252	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0001270	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0007153	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83472	CAMOS syndrome		HP:0007360	ORPHA:83472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0005359	ORPHA:83471	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002719	ORPHA:83471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0005352	ORPHA:83471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0005374	ORPHA:83471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0005403	ORPHA:83471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0031381	ORPHA:83471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0031397	ORPHA:83471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0001508	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002090	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002718	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002960	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0004798	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0031690	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0031691	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0032169	ORPHA:83471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0000010	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0000246	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0000389	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0000821	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0000964	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0001287	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002014	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002024	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002716	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0002726	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0003472	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0004844	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0005366	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0005387	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0005401	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0009098	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0020101	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0031430	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0100646	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0100806	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83471	T-cell immunodeficiency with thymic aplasia		HP:0200122	ORPHA:83471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0000407	ORPHA:137867	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0001283	ORPHA:137867	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0001621	ORPHA:137867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0002460	ORPHA:137867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0003487	ORPHA:137867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0003693	ORPHA:137867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0006801	ORPHA:137867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0007289	ORPHA:137867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0000360	ORPHA:137867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0000505	ORPHA:137867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0000648	ORPHA:137867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0001315	ORPHA:137867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0001317	ORPHA:137867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0002015	ORPHA:137867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0100753	ORPHA:137867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0007663	ORPHA:137867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137867	Madras motor neuron disease		HP:0010628	ORPHA:137867	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000054	ORPHA:75858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000505	ORPHA:75858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000750	ORPHA:75858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0001956	ORPHA:75858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000518	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000556	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000718	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000752	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0001105	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0001256	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0002342	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0002465	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0007675	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0010864	ORPHA:75858	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome		HP:0000077	ORPHA:75858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome	NOT	HP:0000613	ORPHA:75858	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome	NOT	HP:0000639	ORPHA:75858	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:75858	MORM syndrome	NOT	HP:0001252	ORPHA:75858	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000046	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000069	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000135	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000164	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000204	ORPHA:3253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000347	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000400	ORPHA:3253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000411	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000431	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000494	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000664	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000668	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000670	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000674	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000682	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000966	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000968	ORPHA:3253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0000972	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0001249	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0001250	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0001596	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0001770	ORPHA:3253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0001810	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0002167	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0002205	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0002353	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0002553	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0100337	ORPHA:3253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0003307	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0003777	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0005338	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0006101	ORPHA:3253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0006482	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0006610	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0007477	ORPHA:3253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0007598	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0008070	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0008391	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0008404	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0010669	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0011800	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3253	Cleft lip/palate-ectodermal dysplasia syndrome		HP:0100840	ORPHA:3253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000047	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000256	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000268	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000289	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000294	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000316	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000347	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000358	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000470	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000486	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000540	ORPHA:75857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000639	ORPHA:75857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000750	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001263	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000771	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0000962	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001357	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001250	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001256	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001310	ORPHA:75857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001321	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001382	ORPHA:75857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001508	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001513	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001741	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001822	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001884	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0001999	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002066	ORPHA:75857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002079	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002126	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002269	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002282	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002500	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002521	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002538	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002553	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002650	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0002705	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0005487	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0006610	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0006712	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0007165	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0008947	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0011220	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0012471	ORPHA:75857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0030084	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0012745	ORPHA:75857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75857	6q terminal deletion syndrome		HP:0030048	ORPHA:75857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0001250	ORPHA:99802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0025373	ORPHA:99802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0030890	ORPHA:99802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0000267	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0000929	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0001263	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0002119	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0002126	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0002392	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0007206	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0010851	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0011153	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0011193	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0011195	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0011215	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0032046	ORPHA:99802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0000256	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0000648	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0001269	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0001302	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0001336	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0002133	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0002171	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0002282	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0004302	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0006824	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0010819	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0010864	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0011097	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0011167	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0012246	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0012377	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99802	Hemimegalencephaly		HP:0012757	ORPHA:99802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0000486	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001508	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001518	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0002251	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0005957	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0007110	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0010536	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0012332	ORPHA:99803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001249	ORPHA:99803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001250	ORPHA:99803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001252	ORPHA:99803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001522	ORPHA:99803	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0002020	ORPHA:99803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0000407	ORPHA:99803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001558	ORPHA:99803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001561	ORPHA:99803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0001562	ORPHA:99803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0003005	ORPHA:99803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99803	Haddad syndrome		HP:0003006	ORPHA:99803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000028	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000252	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000426	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000430	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000431	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000445	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001249	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001263	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001328	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0002300	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0002381	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0003510	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0004209	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0010529	ORPHA:3255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000322	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000337	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000494	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000648	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001252	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001257	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001376	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001510	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001511	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001792	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001864	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0002007	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0002451	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0002750	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0004322	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0007598	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0010550	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0010580	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0010624	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0010761	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0011220	ORPHA:3255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0000233	ORPHA:3255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001250	ORPHA:3255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0001629	ORPHA:3255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0002558	ORPHA:3255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3255	Filippi syndrome		HP:0006101	ORPHA:3255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0001817	ORPHA:3258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0002007	ORPHA:3258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0005048	ORPHA:3258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0005916	ORPHA:3258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0006101	ORPHA:3258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0012165	ORPHA:3258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0100240	ORPHA:3258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000316	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000494	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0001770	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0001802	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0002974	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0002984	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0003022	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0009778	ORPHA:3258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000272	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000322	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000365	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000411	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000444	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000508	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000518	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000520	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000639	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000656	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000668	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000682	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000772	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0000821	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0001601	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0001849	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0002650	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0002705	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0002827	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0002983	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0003042	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0003196	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0003312	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0004736	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0007477	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3258	Cenani-Lenz syndrome		HP:0008678	ORPHA:3258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0012301	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0030282	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000160	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000218	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000253	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000316	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000343	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000347	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000431	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000475	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000494	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001290	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001433	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0002342	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0002673	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0002751	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0003180	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0003422	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0007033	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0007112	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0008551	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0011342	ORPHA:263508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000201	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000219	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000319	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000358	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000470	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000902	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0000938	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001103	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001256	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001320	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001508	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001762	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0001999	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0002092	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0002280	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0003026	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0003316	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0004582	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0008897	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0008905	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263508	COG1-CDG		HP:0011995	ORPHA:263508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0012347	ORPHA:263501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0012358	ORPHA:263501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0000252	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0000340	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0000639	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0000737	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001251	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001263	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001344	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001347	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001394	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001433	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001510	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001531	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0001873	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0002254	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0002509	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0002788	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0002910	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0003124	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0003155	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0003256	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0006892	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0008935	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0008936	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0011172	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0011968	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0012301	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0100874	ORPHA:263501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0002079	ORPHA:263501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0004798	ORPHA:263501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0006583	ORPHA:263501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263501	COG4-CDG		HP:0040187	ORPHA:263501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0011380	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0011800	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000119	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000175	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000193	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000238	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000388	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000407	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000453	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000505	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000648	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0002032	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0002093	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0002119	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0002308	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0002676	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0002983	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0004397	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0006536	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0008404	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0012803	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0030680	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0100702	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0200020	ORPHA:87	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000244	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000327	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000337	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000405	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000520	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0001363	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0001770	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0002007	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0004440	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0004487	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0005280	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0006101	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0012368	ORPHA:87	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000189	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000239	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000303	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000316	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000324	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000444	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000486	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000494	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000586	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000678	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000684	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000689	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000822	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0000975	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0001249	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0001274	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0001331	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0003422	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0004635	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0008872	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0009601	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87	Apert syndrome		HP:0011304	ORPHA:87	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0001047	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0001250	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0001321	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0001344	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0001347	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0001510	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002171	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002376	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002506	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002510	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002599	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0003281	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0004463	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0004840	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0007346	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0008568	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0008936	ORPHA:3240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0001873	ORPHA:3240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002013	ORPHA:3240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002014	ORPHA:3240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome		HP:0002878	ORPHA:3240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome	NOT	HP:0001332	ORPHA:3240	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3240	Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome	NOT	HP:0011002	ORPHA:3240	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000164	ORPHA:3241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000174	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000200	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000322	ORPHA:3241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000324	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000407	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000430	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000431	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000490	ORPHA:3241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0000582	ORPHA:3241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0001643	ORPHA:3241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0002007	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0004524	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3241	Deafness-craniofacial syndrome		HP:0010297	ORPHA:3241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0001896	ORPHA:88	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0000225	ORPHA:88	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0000421	ORPHA:88	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0000573	ORPHA:88	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0001873	ORPHA:88	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0001875	ORPHA:88	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0002719	ORPHA:88	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0031364	ORPHA:88	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia	NOT	HP:0030057	ORPHA:88	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0001903	ORPHA:88	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0005528	ORPHA:88	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88	Idiopathic aplastic anemia		HP:0001876	ORPHA:88	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0012721	ORPHA:83454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0100026	ORPHA:83454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0011297	ORPHA:83454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0200036	ORPHA:83454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0002814	ORPHA:83454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0002817	ORPHA:83454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0011354	ORPHA:83454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0011355	ORPHA:83454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0200034	ORPHA:83454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0200035	ORPHA:83454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0002629	ORPHA:83454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0002778	ORPHA:83454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0010640	ORPHA:83454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0012210	ORPHA:83454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0031445	ORPHA:83454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83454	Glomuvenous malformation		HP:0045026	ORPHA:83454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0000230	ORPHA:83453	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0000055	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0000155	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0000989	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0001036	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0010783	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0011118	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0012531	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0012537	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0025092	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0100725	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0200041	ORPHA:83453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83453	Vulvovaginal gingival syndrome		HP:0001807	ORPHA:83453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0009763	ORPHA:83452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0000958	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0003474	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0004305	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0008383	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0010741	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0010742	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0010783	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0010834	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0012533	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0012534	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83452	Complex regional pain syndrome		HP:0040170	ORPHA:83452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0000277	ORPHA:83451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0000326	ORPHA:83451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0003330	ORPHA:83451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0100671	ORPHA:83451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0100717	ORPHA:83451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0000309	ORPHA:83451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0000700	ORPHA:83451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0001571	ORPHA:83451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0430028	ORPHA:83451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0000155	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0000689	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0006308	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0006481	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0006483	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0007626	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0009088	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0010885	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0011069	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0011968	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0012065	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0012531	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0030793	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83451	Florid cemento-osseous dysplasia		HP:0031035	ORPHA:83451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0000568	ORPHA:83461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0001087	ORPHA:83461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0007707	ORPHA:83461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0008062	ORPHA:83461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0000504	ORPHA:83461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0000541	ORPHA:83461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0000588	ORPHA:83461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0000647	ORPHA:83461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0007973	ORPHA:83461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0011483	ORPHA:83461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0000526	ORPHA:83461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0000667	ORPHA:83461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83461	Congenital primary aphakia		HP:0100583	ORPHA:83461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0011397	ORPHA:137898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001260	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001317	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001337	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002073	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002167	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002191	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002312	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002317	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001288	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002460	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002493	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002497	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002505	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0003487	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0006978	ORPHA:137898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001265	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001268	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001270	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001315	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001328	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002151	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002166	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002490	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0003477	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0006858	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0007010	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0008969	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0010794	ORPHA:137898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0000365	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0000508	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0000514	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0000639	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0000648	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0000651	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001249	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001250	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001252	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001271	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001272	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001276	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001344	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001350	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0001371	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002059	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002078	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0002079	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0005340	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0007668	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137898	Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome		HP:0009055	ORPHA:137898	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001324	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002093	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002206	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002960	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0003326	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0006530	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0012735	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0100614	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0100749	ORPHA:81	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0000217	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0000969	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001097	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001252	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001369	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001945	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002094	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002829	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0003236	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0003457	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0030880	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034143	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034145	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034146	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034147	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034148	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034149	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034150	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034151	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034152	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0034153	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0100679	ORPHA:81	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0000988	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0000989	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001373	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001608	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0001659	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002015	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002092	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002205	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0002664	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0012819	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:0100585	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:6001013	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:81	Antisynthetase syndrome		HP:6001014	ORPHA:81	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000252	ORPHA:3242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0001249	ORPHA:3242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0003202	ORPHA:3242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0003510	ORPHA:3242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0004326	ORPHA:3242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000047	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000272	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000274	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000275	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000276	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000286	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000303	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000322	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000400	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000448	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000582	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000772	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000912	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0001510	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0001596	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0008734	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0045074	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0100830	ORPHA:3242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000160	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000175	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000407	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000486	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000518	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000612	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000767	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0000819	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0001172	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0001250	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0001387	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0001572	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0002023	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0002705	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0003328	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0004209	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0008499	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0010761	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3242	Renpenning syndrome		HP:0030853	ORPHA:3242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0000365	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0000524	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0000618	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0000639	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0000648	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0000763	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0002066	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0002073	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0002166	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0002346	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0001288	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0002464	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0005102	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0006254	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0007126	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0007141	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0007263	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome		HP:0008180	ORPHA:95433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95433	Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome	NOT	HP:0000657	ORPHA:95433	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0001976	ORPHA:82	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0040246	ORPHA:82	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0002204	ORPHA:82	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0002625	ORPHA:82	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0002638	ORPHA:82	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0004831	ORPHA:82	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0031437	ORPHA:82	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0004420	ORPHA:82	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0005268	ORPHA:82	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0012636	ORPHA:82	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0030242	ORPHA:82	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0030243	ORPHA:82	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0030248	ORPHA:82	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0200067	ORPHA:82	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:82	Hereditary thrombophilia due to congenital antithrombin deficiency		HP:0005305	ORPHA:82	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0200039	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0001644	ORPHA:3243	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0003002	ORPHA:3243	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0005550	ORPHA:3243	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0012531	ORPHA:3243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0025474	ORPHA:3243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0030350	ORPHA:3243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0011117	ORPHA:3243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0031236	ORPHA:3243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0200036	ORPHA:3243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0000271	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0000464	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0001061	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0001155	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0001974	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0002829	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0003326	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0003565	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0011118	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0011227	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0011897	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0011944	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0025616	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0030783	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0032324	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0100614	ORPHA:3243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0001903	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0002037	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0002664	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0002719	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0004377	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0004808	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0008066	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0012490	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0020169	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0025452	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0040154	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0040313	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3243	Sweet syndrome		HP:0200037	ORPHA:3243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000248	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000270	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000358	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000463	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000772	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000774	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0001166	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0001387	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0002007	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0002980	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0003070	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0003196	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0003275	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0010669	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0030680	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0100490	ORPHA:83	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000453	ORPHA:83	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000520	ORPHA:83	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0001363	ORPHA:83	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0012210	ORPHA:83	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000160	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000175	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000262	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000316	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000343	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000486	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0000494	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0001883	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0002757	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83	Antley-Bixler syndrome		HP:0009891	ORPHA:83	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002779	ORPHA:95430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0004468	ORPHA:95430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001601	ORPHA:95430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002093	ORPHA:95430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002788	ORPHA:95430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0010307	ORPHA:95430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0012735	ORPHA:95430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0030828	ORPHA:95430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0032355	ORPHA:95430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0000961	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0000973	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001508	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001609	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001622	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001627	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001686	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002020	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002032	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002090	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002094	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002107	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002575	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002643	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0011968	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0012758	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0030864	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0030966	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0031245	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0032177	ORPHA:95430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001629	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001631	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001636	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001640	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001643	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0001750	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002089	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002092	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002097	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002104	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002110	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002780	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0002786	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0010773	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0011590	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95430	Congenital tracheomalacia		HP:0012020	ORPHA:95430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001000	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001053	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001172	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001871	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001873	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001882	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001903	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002817	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0003220	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0004322	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0005522	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0006501	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0007400	ORPHA:84	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000079	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000252	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001249	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001263	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001671	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002650	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002664	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0007874	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0012210	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0012745	ORPHA:84	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000010	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000027	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000028	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000035	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000047	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000072	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000083	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000130	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000135	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000175	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000218	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000238	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000268	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000286	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000316	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000324	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000340	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000347	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000364	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000365	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000453	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000478	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000483	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000486	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000492	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000504	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000505	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000508	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000518	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000520	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000568	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000582	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000639	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000813	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000864	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001199	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001347	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001392	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001510	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001511	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001537	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001562	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001631	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001636	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001639	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001643	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001646	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001679	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001760	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001763	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001770	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0001824	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002007	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002023	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002119	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002245	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002251	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002414	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002575	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002823	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002827	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0002863	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0003022	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0004209	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0004349	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0005344	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0006101	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0006265	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0006824	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0007565	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0008053	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0000377	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0008678	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0010293	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0010469	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0012041	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0012639	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0040071	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0100026	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0100542	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0100587	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0100760	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84	Fanconi anemia		HP:0100867	ORPHA:84	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0004197	ORPHA:3246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0004218	ORPHA:3246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0006019	ORPHA:3246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0000256	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0001032	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0001156	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0001245	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0001770	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0005807	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0006101	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0007477	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0009700	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0010179	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0010182	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0010487	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0030084	ORPHA:3246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0000405	ORPHA:3246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0001018	ORPHA:3246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0005650	ORPHA:3246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0006143	ORPHA:3246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0010103	ORPHA:3246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3246	Symphalangism with multiple anomalies of hands and feet		HP:0100371	ORPHA:3246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3248	Isolated distal symphalangism		HP:0005048	ORPHA:3248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3248	Isolated distal symphalangism		HP:0001387	ORPHA:3248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3248	Isolated distal symphalangism		HP:0009773	ORPHA:3248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3248	Isolated distal symphalangism		HP:0100490	ORPHA:3248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002066	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002070	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002073	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002078	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002366	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002493	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0003474	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0007256	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0025404	ORPHA:95434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0000496	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0000570	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0001260	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0001761	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002317	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0002380	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0007141	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0007338	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0010522	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0010831	ORPHA:95434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95434	Autosomal recessive cerebellar ataxia-movement disorder syndrome		HP:0001336	ORPHA:95434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034098	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034099	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034100	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034101	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0100758	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0025420	ORPHA:80	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001511	ORPHA:80	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0000822	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001622	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0002140	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0002326	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0003613	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0004420	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0004936	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0008222	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0012378	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0012531	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0020136	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0020137	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0025343	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0032376	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0033260	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0033505	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034156	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034157	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0100602	ORPHA:80	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0100724	ORPHA:80	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0000093	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001250	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001268	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001638	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001650	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001653	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001659	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001718	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0001873	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0002092	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034084	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:80	Antiphospholipid syndrome		HP:0034097	ORPHA:80	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001251	ORPHA:96	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001284	ORPHA:96	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001324	ORPHA:96	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0003487	ORPHA:96	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0007256	ORPHA:96	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0009830	ORPHA:96	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0100513	ORPHA:96	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000639	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000662	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000763	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001260	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001272	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001288	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001310	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001761	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0002075	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0002167	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0002312	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0002599	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0002650	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0010831	ORPHA:96	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000012	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000505	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000649	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000819	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001268	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001276	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001332	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001337	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0001639	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0002376	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0002403	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0003202	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0004374	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0007703	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0011675	ORPHA:96	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96	Ataxia with vitamin E deficiency		HP:0000580	ORPHA:96	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0001263	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0001332	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0002072	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0002310	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0002322	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0001288	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0003557	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0003687	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0003701	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0004305	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0007153	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0007158	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0009046	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0012751	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0030230	ORPHA:401768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0000252	ORPHA:401768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0000508	ORPHA:401768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0000602	ORPHA:401768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0000648	ORPHA:401768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0001251	ORPHA:401768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0003477	ORPHA:401768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs		HP:0008180	ORPHA:401768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs	NOT	HP:0000365	ORPHA:401768	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs	NOT	HP:0000831	ORPHA:401768	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:401768	Proximal myopathy with extrapyramidal signs	NOT	HP:0001638	ORPHA:401768	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0000639	ORPHA:97	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0001251	ORPHA:97	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0002321	ORPHA:97	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0000360	ORPHA:97	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0000651	ORPHA:97	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0001260	ORPHA:97	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0001332	ORPHA:97	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0002017	ORPHA:97	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0002076	ORPHA:97	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0002301	ORPHA:97	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0000473	ORPHA:97	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0000708	ORPHA:97	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0001249	ORPHA:97	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97	Familial paroxysmal ataxia		HP:0006855	ORPHA:97	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0000020	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001251	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001257	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001260	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001272	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001310	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001317	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001320	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001324	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001634	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002061	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002073	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002079	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002317	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001288	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0003487	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0007108	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0007141	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0007256	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0007361	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0007922	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0007979	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0009830	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0011931	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0012104	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0012896	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0100702	ORPHA:98	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0000708	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0001760	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002015	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002066	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002080	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0002495	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0003438	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0003693	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0009027	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0010830	ORPHA:98	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		HP:0000802	ORPHA:98	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3230	Deafness-oligodontia syndrome		HP:0000359	ORPHA:3230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3230	Deafness-oligodontia syndrome		HP:0000407	ORPHA:3230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3230	Deafness-oligodontia syndrome		HP:0000677	ORPHA:3230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3230	Deafness-oligodontia syndrome		HP:0002321	ORPHA:3230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95429	Angioma serpiginosum		HP:0007797	ORPHA:95429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95429	Angioma serpiginosum		HP:0010783	ORPHA:95429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95429	Angioma serpiginosum		HP:0011276	ORPHA:95429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95429	Angioma serpiginosum		HP:0012733	ORPHA:95429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3239	Deafness-vitiligo-achalasia syndrome		HP:0000407	ORPHA:3239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3239	Deafness-vitiligo-achalasia syndrome		HP:0001053	ORPHA:3239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3239	Deafness-vitiligo-achalasia syndrome		HP:0002353	ORPHA:3239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3239	Deafness-vitiligo-achalasia syndrome		HP:0002571	ORPHA:3239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3239	Deafness-vitiligo-achalasia syndrome		HP:0003202	ORPHA:3239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3239	Deafness-vitiligo-achalasia syndrome		HP:0003510	ORPHA:3239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001824	ORPHA:95427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002024	ORPHA:95427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002244	ORPHA:95427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0004395	ORPHA:95427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0100508	ORPHA:95427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0000832	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001396	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001508	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001510	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001543	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001944	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001977	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002013	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002014	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002019	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002570	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002580	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002591	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002621	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0003111	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0003270	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0003572	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0004387	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0011473	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0012850	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0030247	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0030248	ORPHA:95427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0001265	ORPHA:95427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0002251	ORPHA:95427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0011100	ORPHA:95427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0011787	ORPHA:95427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95427	Secondary short bowel syndrome		HP:0100806	ORPHA:95427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001249	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001250	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001251	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001508	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0002243	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0002376	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0002421	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0002465	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0003202	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0007267	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0008947	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0011344	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0012537	ORPHA:95428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0000253	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001137	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001272	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001336	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0001943	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0002119	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0002910	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0006846	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0007366	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0007420	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95428	COG8-CDG		HP:0008151	ORPHA:95428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000230	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000670	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000682	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000684	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000694	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000706	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0003771	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0006286	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0006297	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0006479	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0006481	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0009722	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0010299	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0011073	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0011084	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0030757	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0040264	ORPHA:83450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000212	ORPHA:83450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0000685	ORPHA:83450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0001572	ORPHA:83450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0006283	ORPHA:83450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0006336	ORPHA:83450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0009085	ORPHA:83450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83450	Regional odontodysplasia		HP:0200025	ORPHA:83450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0003251	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008214	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008232	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008665	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008726	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008730	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008734	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008736	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0010464	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0011969	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0012244	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0012870	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0040171	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0100779	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000028	ORPHA:251510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000150	ORPHA:251510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000823	ORPHA:251510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000030	ORPHA:251510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000149	ORPHA:251510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000846	ORPHA:251510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0002750	ORPHA:251510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008187	ORPHA:251510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0008193	ORPHA:251510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000100	ORPHA:251510	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0002667	ORPHA:251510	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0030680	ORPHA:251510	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000027	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000045	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000047	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000054	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000058	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000062	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000133	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000142	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000771	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000786	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000812	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000815	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000837	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000868	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0000939	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0002215	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251510	46,XY partial gonadal dysgenesis		HP:0002225	ORPHA:251510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0007628	ORPHA:137888	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000377	ORPHA:137888	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0009902	ORPHA:137888	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000160	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000162	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000175	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000183	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000193	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000293	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000324	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000347	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000358	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000377	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000384	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000678	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000689	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0002098	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0002870	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0008772	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0009895	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0010754	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0025267	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0030022	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0100277	ORPHA:137888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000171	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000256	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000365	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0000508	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0001263	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0001290	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0007627	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0011802	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0011968	ORPHA:137888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137888	Auriculocondylar syndrome		HP:0030713	ORPHA:137888	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000212	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000303	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000316	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000431	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000750	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001249	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001537	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001999	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002167	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002650	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0003196	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0004337	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0008551	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0012068	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0012471	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0100660	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0100729	ORPHA:93	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000053	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000158	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000164	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000280	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000670	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000768	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002684	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0003103	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0008430	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0040071	ORPHA:93	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000023	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000389	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0000708	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001250	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001369	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001387	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001744	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0001763	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002024	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002205	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002240	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002360	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0002750	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0003468	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0004568	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93	Aspartylglucosaminuria		HP:0011276	ORPHA:93	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0000383	ORPHA:3232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0000405	ORPHA:3232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0000377	ORPHA:3232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0008628	ORPHA:3232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0009738	ORPHA:3232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0009739	ORPHA:3232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0009906	ORPHA:3232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3232	Deafness-ear malformation-facial palsy syndrome		HP:0010628	ORPHA:3232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3233	Cochleosaccular degeneration-cataract syndrome		HP:0000408	ORPHA:3233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3233	Cochleosaccular degeneration-cataract syndrome		HP:0000518	ORPHA:3233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3233	Cochleosaccular degeneration-cataract syndrome		HP:0005102	ORPHA:3233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3233	Cochleosaccular degeneration-cataract syndrome		HP:0001251	ORPHA:3233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3233	Cochleosaccular degeneration-cataract syndrome		HP:0001250	ORPHA:3233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002522	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002527	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002650	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002839	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0003115	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0003390	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0003394	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0007010	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0010873	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0012079	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0012452	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0030183	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000365	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002066	ORPHA:95	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001260	ORPHA:95	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002070	ORPHA:95	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002141	ORPHA:95	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0003487	ORPHA:95	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0009130	ORPHA:95	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0010831	ORPHA:95	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000012	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000570	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000639	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000648	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001063	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001310	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001324	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001638	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001760	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001761	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001762	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002037	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002080	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002270	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002312	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002495	ORPHA:95	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000716	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000739	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0000819	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001257	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001272	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001332	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0001618	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002015	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002075	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002540	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002546	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0003431	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0004349	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0007663	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0010535	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0025402	ORPHA:95	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95	Friedreich ataxia		HP:0002072	ORPHA:95	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3235	Progressive deafness with stapes fixation		HP:0000381	ORPHA:3235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3235	Progressive deafness with stapes fixation		HP:0008513	ORPHA:3235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000174	ORPHA:3236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000286	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000405	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000413	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000446	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000508	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000545	ORPHA:3236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000581	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0000682	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0002213	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0003042	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0003272	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0004209	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0007477	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0007598	ORPHA:3236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3236	Conductive deafness-ptosis-skeletal anomalies syndrome		HP:0008773	ORPHA:3236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0000708	ORPHA:90	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0001250	ORPHA:90	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0001263	ORPHA:90	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0001987	ORPHA:90	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0002167	ORPHA:90	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0002353	ORPHA:90	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0002478	ORPHA:90	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0004374	ORPHA:90	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0008339	ORPHA:90	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90	Argininemia		HP:0010864	ORPHA:90	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0000405	ORPHA:3237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0001156	ORPHA:3237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0001387	ORPHA:3237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0004279	ORPHA:3237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0009773	ORPHA:3237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0007598	ORPHA:3237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0010579	ORPHA:3237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0011304	ORPHA:3237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0000324	ORPHA:3237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3237	Multiple synostoses syndrome		HP:0001597	ORPHA:3237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000938	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000939	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0001510	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0001513	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0002653	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0002663	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0002750	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0002857	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0003077	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0003251	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0003782	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0008072	ORPHA:91	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0008222	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0008675	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0010458	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000855	ORPHA:91	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000956	ORPHA:91	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0001397	ORPHA:91	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0002050	ORPHA:91	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0002230	ORPHA:91	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0005978	ORPHA:91	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000028	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000061	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000098	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000786	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91	Aromatase deficiency		HP:0000815	ORPHA:91	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0000405	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0001156	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0001634	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0001653	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0002705	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0003312	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0003510	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0004279	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0005048	ORPHA:3238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0000692	ORPHA:3238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3238	Cardiospondylocarpofacial syndrome		HP:0006352	ORPHA:3238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0001824	ORPHA:67	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002014	ORPHA:67	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002027	ORPHA:67	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002579	ORPHA:67	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0004385	ORPHA:67	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0025085	ORPHA:67	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0100749	ORPHA:67	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0001635	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0001697	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0001903	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0001945	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0001974	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002094	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002105	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002202	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002563	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002625	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0002910	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0003073	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0003155	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0005214	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0011919	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0012735	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0025044	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0032016	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0100282	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67	Amoebiasis due to Entamoeba histolytica		HP:0100523	ORPHA:67	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000613	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000708	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000751	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001250	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001945	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002013	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002018	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002315	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002383	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002921	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002922	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0200149	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0410263	ORPHA:68	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000324	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000572	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000651	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000711	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000737	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001254	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001269	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001289	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001317	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002134	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002143	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002181	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002381	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002418	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002500	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002516	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002538	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002721	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0006897	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0007011	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0007185	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0007361	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0010628	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0011441	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0012246	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0012286	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0012747	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0020059	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0025258	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0031179	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0031910	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0032252	ORPHA:68	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000223	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000246	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000618	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0000834	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001251	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001259	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001482	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0001700	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0002090	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0004409	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0011675	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0011947	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0012804	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0030953	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0031731	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0032162	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0032620	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0040197	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0100583	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0200026	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0200034	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0200039	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:68	Amoebiasis due to free-living amoebae		HP:0200042	ORPHA:68	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000586	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000765	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000883	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0001344	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0002015	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0002020	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0002100	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0002119	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0002194	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0003100	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0003199	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0003244	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0003312	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0008897	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0009237	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0009875	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0009882	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0031207	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0100759	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000774	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000940	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0001263	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0001290	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0002240	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0002910	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0003016	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0006462	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0011849	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0100774	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000239	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000325	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000463	ORPHA:73230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000316	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000347	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000348	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73230	Ossification anomalies-psychomotor developmental delay syndrome		HP:0000520	ORPHA:73230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000790	ORPHA:63	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0012577	ORPHA:63	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0030034	ORPHA:63	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000083	ORPHA:63	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000093	ORPHA:63	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000822	ORPHA:63	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0012574	ORPHA:63	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000092	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000097	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000100	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000123	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000407	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000478	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000495	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000794	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0002907	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0003774	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0004722	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0005576	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0011488	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0011501	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0012045	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0012576	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0025005	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0032583	ORPHA:63	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0000608	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0001679	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0002013	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0002015	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0002094	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0002837	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0004942	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0006756	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0007787	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0008665	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0010307	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0012735	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63	Alport syndrome		HP:0410019	ORPHA:63	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002091	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002591	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002788	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002808	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002910	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002943	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0003474	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0004438	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0004469	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0004626	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0005978	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0006532	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0007722	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0008373	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0010863	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0011108	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0012622	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0025383	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0030948	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0031865	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000010	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000012	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000016	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000020	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000054	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000099	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000147	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000230	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000311	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000490	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000729	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000771	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000798	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000824	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000832	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000858	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001007	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001123	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001394	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001395	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001397	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001399	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001409	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001433	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001635	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001685	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001744	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001751	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001831	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002020	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002040	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002092	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002098	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002213	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002240	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002292	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002311	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002925	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0003774	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0005616	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0006510	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0007010	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0007787	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0008625	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0008734	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0009381	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0009804	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0009894	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0010790	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0011073	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0011510	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0012041	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0012115	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0012786	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0012860	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0025335	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0025336	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0025488	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0025496	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0030348	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0031507	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0031936	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0100518	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0410019	ORPHA:64	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001251	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001733	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002360	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002480	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0003326	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0010465	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0011147	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0012569	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0100543	ORPHA:64	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000388	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000408	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000548	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000556	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000572	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000618	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000639	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000855	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001513	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0002155	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0003077	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0004322	ORPHA:64	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000009	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000518	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000543	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000613	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000815	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000822	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000842	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0000956	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001328	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001644	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001763	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64	Alström syndrome		HP:0001956	ORPHA:64	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0001141	ORPHA:65	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0007703	ORPHA:65	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0012795	ORPHA:65	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000512	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000518	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000540	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000563	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000613	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000639	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0001250	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0001252	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0001483	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0002084	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0002269	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0004374	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0006817	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0030211	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0030466	ORPHA:65	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000365	ORPHA:65	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000543	ORPHA:65	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0000729	ORPHA:65	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0001249	ORPHA:65	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0001263	ORPHA:65	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0001270	ORPHA:65	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65	Leber congenital amaurosis		HP:0012426	ORPHA:65	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000648	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000729	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001249	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001250	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001252	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001263	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001999	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0002079	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0007663	ORPHA:401777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000286	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000365	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000411	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000426	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000463	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000486	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000565	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000577	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000582	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000609	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000646	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000722	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001123	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001182	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001344	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0003194	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0007018	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0007766	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0008762	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0011039	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0100704	ORPHA:401777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000540	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000545	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000563	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0000639	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0001257	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0002750	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0004322	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0012448	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401777	Optic atrophy-intellectual disability syndrome		HP:0025100	ORPHA:401777	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001522	ORPHA:85212	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001558	ORPHA:85212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001876	ORPHA:85212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0002804	ORPHA:85212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0003811	ORPHA:85212	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0003826	ORPHA:85212	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0007479	ORPHA:85212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0008064	ORPHA:85212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0000218	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0000358	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0000463	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0000656	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001252	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001371	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001433	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001508	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001873	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001903	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0002908	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0003656	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0005280	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0031956	ORPHA:85212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0000238	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001250	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001276	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0001790	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0002020	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0002033	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0002170	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0002179	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85212	Fetal Gaucher disease		HP:0007957	ORPHA:85212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000023	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000112	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000280	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000365	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000750	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000768	ORPHA:87876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000939	ORPHA:87876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0000943	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001103	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001250	ORPHA:87876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001251	ORPHA:87876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001263	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001290	ORPHA:87876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001324	ORPHA:87876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001337	ORPHA:87876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001371	ORPHA:87876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001537	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001541	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001618	ORPHA:87876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001744	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0001789	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0002094	ORPHA:87876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0002240	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0002808	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0003202	ORPHA:87876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0004322	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0005561	ORPHA:87876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0007957	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0010306	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0010741	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87876	Sialidosis type 2		HP:0100022	ORPHA:87876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73229	HANAC syndrome		HP:0000083	ORPHA:73229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73229	HANAC syndrome		HP:0003394	ORPHA:73229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73229	HANAC syndrome		HP:0005562	ORPHA:73229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73229	HANAC syndrome		HP:0012841	ORPHA:73229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73229	HANAC syndrome		HP:0000790	ORPHA:73229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0001231	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0001249	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0003241	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0003777	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0008388	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0011362	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0045074	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0100643	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000311	ORPHA:3220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000786	ORPHA:3220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0001176	ORPHA:3220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0004322	ORPHA:3220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0011675	ORPHA:3220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000763	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000956	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0001265	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0002514	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0002750	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0008064	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0009830	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0009890	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0010547	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0100490	ORPHA:3220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000135	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000164	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000365	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000407	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000492	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000534	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000614	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000679	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000682	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3220	Deafness-enamel hypoplasia-nail defects syndrome		HP:0000819	ORPHA:3220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0045051	ORPHA:60	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0000100	ORPHA:60	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0001396	ORPHA:60	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0006510	ORPHA:60	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0032229	ORPHA:60	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0001402	ORPHA:60	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0001399	ORPHA:60	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0002097	ORPHA:60	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0002110	ORPHA:60	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0032025	ORPHA:60	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0000952	ORPHA:60	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0001394	ORPHA:60	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0002240	ORPHA:60	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0012115	ORPHA:60	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0012387	ORPHA:60	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60	Alpha-1-antitrypsin deficiency		HP:0012490	ORPHA:60	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0003396	ORPHA:99857	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0040272	ORPHA:99857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0000224	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0001618	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0001288	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0002922	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0003401	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0003418	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0003473	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0003474	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0006824	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0007209	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0010532	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0010550	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0010871	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0012229	ORPHA:99857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0000622	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0000639	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0001250	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0001283	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0002073	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0002858	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0003409	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0007024	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0007305	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99857	Secondary syringomyelia		HP:0100518	ORPHA:99857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0003565	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0030153	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0032106	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0100523	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0100806	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0100889	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome	NOT	HP:0001405	ORPHA:480520	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001406	ORPHA:480520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0011040	ORPHA:480520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0000077	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0000952	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001945	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002027	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002240	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002904	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002908	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0003155	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0025143	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0030151	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0032545	ORPHA:480520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0000113	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0000989	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001394	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001399	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001409	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001733	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001873	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001882	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001892	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001971	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0001974	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002040	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002248	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002249	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002612	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480520	Caroli syndrome		HP:0002910	ORPHA:480520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000158	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000280	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000365	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000518	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0001249	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0001263	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0001744	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0002240	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0002652	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0002750	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0004493	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0005280	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0005978	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0007957	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0008821	ORPHA:61	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000023	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000189	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000212	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000316	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000336	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000389	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000400	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000470	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000708	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0001252	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0001385	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0002650	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0002808	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0006487	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0010807	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0011039	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0011354	ORPHA:61	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000256	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000303	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000687	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000689	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0000738	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0001369	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0002205	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0002516	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0010885	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:61	Alpha-mannosidosis		HP:0100240	ORPHA:61	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0011755	ORPHA:95496	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0000864	ORPHA:95496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0001508	ORPHA:95496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0004322	ORPHA:95496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0000821	ORPHA:95496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0000823	ORPHA:95496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0001943	ORPHA:95496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0008736	ORPHA:95496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0000028	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0000786	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0000835	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0000873	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0001249	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0001250	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0001263	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0001522	ORPHA:95496	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:95496	Pituitary stalk interruption syndrome		HP:0100842	ORPHA:95496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000407	ORPHA:3222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001251	ORPHA:3222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0002149	ORPHA:3222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000083	ORPHA:3222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001249	ORPHA:3222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001252	ORPHA:3222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001679	ORPHA:3222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0002167	ORPHA:3222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000486	ORPHA:3222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000496	ORPHA:3222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0000822	ORPHA:3222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0001638	ORPHA:3222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3222	Phosphoribosylpyrophosphate synthetase superactivity		HP:0011675	ORPHA:3222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0001771	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0002359	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0002515	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003236	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003307	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003391	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003551	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003560	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003691	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003701	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0003707	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0006467	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0030051	ORPHA:62	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:62	Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3		HP:0002943	ORPHA:62	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0001508	ORPHA:99852	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0002039	ORPHA:99852	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0002448	ORPHA:99852	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0004325	ORPHA:99852	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0000932	ORPHA:99852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0001251	ORPHA:99852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0001257	ORPHA:99852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0002134	ORPHA:99852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0002363	ORPHA:99852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0007366	ORPHA:99852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0000496	ORPHA:99852	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0006958	ORPHA:99852	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0001600	ORPHA:99852	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99852	Ravine syndrome		HP:0002104	ORPHA:99852	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000047	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000324	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000358	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000369	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000407	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000411	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0001249	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0001321	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0001761	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0002119	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0002120	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0002334	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0005105	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0005916	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0007477	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0011220	ORPHA:3224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000164	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000286	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0000316	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0001273	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0001596	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0001770	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0001956	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0002167	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0002558	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0003468	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0006101	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3224	Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome		HP:0010109	ORPHA:3224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3225	Hearing loss-familial salivary gland insensitivity to aldosterone syndrome		HP:0000407	ORPHA:3225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3225	Hearing loss-familial salivary gland insensitivity to aldosterone syndrome		HP:0002902	ORPHA:3225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3225	Hearing loss-familial salivary gland insensitivity to aldosterone syndrome		HP:0010286	ORPHA:3225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0001644	ORPHA:73224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0001960	ORPHA:73224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0002150	ORPHA:73224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0002901	ORPHA:73224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0002917	ORPHA:73224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0012608	ORPHA:73224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0000121	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0000859	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0001635	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0001645	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0001698	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0002487	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0002829	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0003472	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0003527	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0003739	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0006559	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0011038	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0100598	ORPHA:73224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73224	Kidney tubulopathy-dilated cardiomyopathy syndrome		HP:0002069	ORPHA:73224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000708	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000718	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000736	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000938	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0001072	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0001382	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0003127	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0007018	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0007387	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0007483	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0010719	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0011125	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0011368	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0025080	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0025160	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0100710	ORPHA:73223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000750	ORPHA:73223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0002353	ORPHA:73223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000233	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000286	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000337	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000343	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000347	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000431	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000574	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000664	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0000689	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0001593	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0001653	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0003307	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0003691	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0005180	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0011065	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0011074	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0011220	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0012365	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0012520	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0040022	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73223	Global developmental delay-osteopenia-ectodermal defect syndrome		HP:0040025	ORPHA:73223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0001934	ORPHA:79	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0005261	ORPHA:79	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0000790	ORPHA:79	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0001892	ORPHA:79	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0012151	ORPHA:79	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0012233	ORPHA:79	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0040247	ORPHA:79	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0000225	ORPHA:79	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0000978	ORPHA:79	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0002170	ORPHA:79	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0002653	ORPHA:79	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79	Congenital alpha2-antiplasmin deficiency		HP:0011884	ORPHA:79	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0002061	ORPHA:401785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0001260	ORPHA:401785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0001347	ORPHA:401785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0001288	ORPHA:401785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0030051	ORPHA:401785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0001284	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0001317	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0002064	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0002169	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0002943	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0003202	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0006380	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401785	Autosomal recessive spastic paraplegia type 62		HP:0012514	ORPHA:401785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0040075	ORPHA:95494	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000044	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000141	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000457	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000789	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000824	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000938	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0001510	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0001943	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0002615	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0002920	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0008245	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0008734	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0009888	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0010311	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0010626	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0010627	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0012378	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0040086	ORPHA:95494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000823	ORPHA:95494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000839	ORPHA:95494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0002019	ORPHA:95494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0002750	ORPHA:95494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0005625	ORPHA:95494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0008187	ORPHA:95494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000478	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0000609	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0001250	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0001274	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0001331	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0001360	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0004637	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0009099	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0010442	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0011297	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0011344	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0011755	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0012731	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95494	Combined pituitary hormone deficiencies, genetic forms		HP:0100842	ORPHA:95494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002315	ORPHA:74	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0012229	ORPHA:74	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0032061	ORPHA:74	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0000651	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0000737	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0001262	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0001287	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0001945	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002013	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002019	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002027	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002516	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002587	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002829	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0003326	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0003401	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0004396	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0011450	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0012378	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0025258	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0032064	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0410263	ORPHA:74	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0000622	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0000989	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0001250	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0001324	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002018	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002119	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002181	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0002460	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0003237	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0003261	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0003496	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0012531	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0030833	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0031179	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0032336	ORPHA:74	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0001259	ORPHA:74	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:74	Angiostrongyliasis		HP:0100963	ORPHA:74	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000003	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000028	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000046	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000126	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000252	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000280	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000316	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000343	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000347	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000365	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000369	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000426	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000445	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000448	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000684	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000750	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0000946	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0001249	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0001250	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0001263	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0001274	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0001631	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0001762	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0002020	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0002089	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0002104	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0002209	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0002213	ORPHA:85201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0002804	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0002974	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0003175	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0003273	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0004279	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0004322	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0006380	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0006443	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0008665	ORPHA:85201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85201	Genitopatellar syndrome		HP:0011968	ORPHA:85201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0000276	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0000340	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0000365	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0000403	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0000430	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0000445	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0000648	ORPHA:85202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0001027	ORPHA:85202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0001250	ORPHA:85202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0001256	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0001263	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0001596	ORPHA:85202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0001629	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0002092	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0002205	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0004322	ORPHA:85202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0004334	ORPHA:85202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0004415	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0005280	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0009882	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0011108	ORPHA:85202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0011800	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0100593	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85202	Keutel syndrome		HP:0100682	ORPHA:85202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85203	Acropectoral syndrome		HP:0000765	ORPHA:85203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85203	Acropectoral syndrome		HP:0001177	ORPHA:85203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85203	Acropectoral syndrome		HP:0006101	ORPHA:85203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0000407	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0002024	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0002028	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0002301	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0002570	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0002588	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0003457	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0004326	ORPHA:3217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0000508	ORPHA:3217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0000600	ORPHA:3217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0001265	ORPHA:3217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0002167	ORPHA:3217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0000496	ORPHA:3217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0000992	ORPHA:3217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0001156	ORPHA:3217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3217	Deafness-small bowel diverticulosis-neuropathy syndrome		HP:0004279	ORPHA:3217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0000872	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0001733	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0003493	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0005200	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0005421	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0030991	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0030992	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0031281	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0032300	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0045042	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0002923	ORPHA:596448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0003212	ORPHA:596448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0003237	ORPHA:596448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0003565	ORPHA:596448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0005339	ORPHA:596448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0011227	ORPHA:596448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0032252	ORPHA:596448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0001744	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0001873	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0001880	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0001882	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0001945	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0032229	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0032235	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0033028	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0033040	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0033555	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0100280	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease	NOT	HP:0100778	ORPHA:596448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:596448	IgG4-related systemic disease		HP:0000315	ORPHA:596448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000023	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000307	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000325	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000365	ORPHA:3218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000470	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000541	ORPHA:3218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000545	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0000579	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0001156	ORPHA:3218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0001256	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0001263	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0001537	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0002007	ORPHA:3218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0002167	ORPHA:3218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0003307	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0003312	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0004322	ORPHA:3218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0006499	ORPHA:3218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3218	Deafness-epiphyseal dysplasia-short stature syndrome		HP:0010306	ORPHA:3218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000154	ORPHA:3219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000174	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000179	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000212	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000232	ORPHA:3219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000256	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000276	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000280	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000282	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000286	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000293	ORPHA:3219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000311	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000316	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000407	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000505	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000508	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000545	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000574	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000664	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000767	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000965	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0000974	ORPHA:3219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0001156	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0005916	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0001176	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0001249	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0001250	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0001482	ORPHA:3219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0001760	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0002167	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0002353	ORPHA:3219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0002414	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0002650	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0002808	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0003298	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0003312	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0004322	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0004493	ORPHA:3219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0009882	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0010783	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0011800	ORPHA:3219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0100255	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0100670	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3219	Fountain syndrome		HP:0200034	ORPHA:3219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0003202	ORPHA:70	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0003701	ORPHA:70	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001283	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001284	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001308	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001315	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002015	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002033	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002100	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001288	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002460	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002540	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002643	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002747	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0003327	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0003551	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0003731	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0004878	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0004891	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0009046	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0012378	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0030319	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0031108	ORPHA:70	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001252	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001263	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001270	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001319	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001349	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001371	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001558	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001631	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002019	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002020	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002091	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002421	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002578	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002650	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002791	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002827	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002828	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002878	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002942	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0003698	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0006380	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0006844	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0008959	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0009053	ORPHA:70	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001662	ORPHA:70	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0001942	ORPHA:70	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70	Proximal spinal muscular atrophy		HP:0002987	ORPHA:70	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0003652	ORPHA:99845	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0001324	ORPHA:99845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0001945	ORPHA:99845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0030234	ORPHA:99845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0040319	ORPHA:99845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0000083	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0001315	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0002910	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0003554	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0003558	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0003738	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0008305	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0010969	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0012544	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0025435	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0100614	ORPHA:99845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0000467	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0001919	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0002153	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0002167	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0001288	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0002901	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0002905	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0003394	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0005216	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0007340	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0008997	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0011675	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0030195	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0045037	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0100520	ORPHA:99845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99845	Genetic recurrent myoglobinuria		HP:0005521	ORPHA:99845	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0002014	ORPHA:71	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0003146	ORPHA:71	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0000488	ORPHA:71	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0002570	ORPHA:71	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0002630	ORPHA:71	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0002910	ORPHA:71	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0001508	ORPHA:71	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0001510	ORPHA:71	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0002013	ORPHA:71	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0003270	ORPHA:71	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0006565	ORPHA:71	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0100508	ORPHA:71	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0000505	ORPHA:71	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0001397	ORPHA:71	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0003458	ORPHA:71	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0001284	ORPHA:71	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0001927	ORPHA:71	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0003198	ORPHA:71	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease		HP:0010831	ORPHA:71	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71	Chylomicron retention disease	NOT	HP:0002155	ORPHA:71	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000252	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000708	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000729	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000748	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000750	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000752	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001250	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001251	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001270	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001337	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002120	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002136	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002167	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002353	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002360	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002465	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0010864	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0011344	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0100716	ORPHA:72	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000154	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000483	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000486	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001010	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001513	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001999	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002019	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002020	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002286	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002307	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002591	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002650	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0006979	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0007730	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0008947	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0010808	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0011024	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0011968	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0100023	ORPHA:72	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000303	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000508	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000540	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000543	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000545	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000563	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000639	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000646	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000648	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000687	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000718	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000739	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0000817	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001336	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0001344	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002013	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002015	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002033	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002123	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002133	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0002540	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0005469	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0007266	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0007270	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0008081	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0010465	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0010819	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0011471	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0012569	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0040082	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0040288	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0100703	ORPHA:72	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:72	Angelman syndrome		HP:0012469	ORPHA:72	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002797	ORPHA:73	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0010639	ORPHA:73	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0010657	ORPHA:73	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0000473	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0000938	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0000969	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002653	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002683	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0003319	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0004302	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0005216	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0005731	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0009139	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0010754	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0011384	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0011821	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0011849	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0012294	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0031417	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0045039	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0100764	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0200025	ORPHA:73	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0000265	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0000365	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0001167	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002202	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002756	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002823	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0007099	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0007461	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0045027	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0430005	ORPHA:73	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0001287	ORPHA:73	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002176	ORPHA:73	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0002754	ORPHA:73	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:73	Gorham-Stout disease		HP:0040163	ORPHA:73	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0004784	ORPHA:480536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0005227	ORPHA:480536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0200063	ORPHA:480536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0000131	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0000854	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0003003	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0004394	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0008069	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0009592	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0012126	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0012740	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0100743	ORPHA:480536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0000107	ORPHA:480536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480536	MSH3-related polyposis		HP:0025274	ORPHA:480536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000407	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000486	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000639	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000684	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000953	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0001053	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0001480	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0001572	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0005599	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0007565	ORPHA:3214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000322	ORPHA:3214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000348	ORPHA:3214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000482	ORPHA:3214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000612	ORPHA:3214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0001288	ORPHA:3214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0007730	ORPHA:3214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0011483	ORPHA:3214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0000679	ORPHA:3214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0001276	ORPHA:3214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0002705	ORPHA:3214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0008499	ORPHA:3214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3214	Deaf blind hypopigmentation syndrome, Yemenite type		HP:0200007	ORPHA:3214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0001257	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0001271	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0001288	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0002815	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0005109	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0007083	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0007178	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401780	Autosomal recessive spastic paraplegia type 61		HP:0012407	ORPHA:401780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001250	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001511	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001518	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001935	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001954	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0002059	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0002360	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0010864	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000010	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000166	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000189	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000212	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000252	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000294	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000303	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000316	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000385	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000403	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000405	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000431	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000457	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000491	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000527	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001169	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001251	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001290	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001347	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001537	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001845	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0002002	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0002028	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0002240	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0005280	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0006480	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0006532	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0006895	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0007041	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0007333	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0008551	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0009826	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0010808	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0011229	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0011341	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0020045	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0031123	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0031629	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0100540	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0100699	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0200037	ORPHA:99843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000280	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001508	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001903	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0001974	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0002719	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0004322	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0011897	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0410292	ORPHA:99843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99843	Leukocyte adhesion deficiency type II		HP:0000729	ORPHA:99843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000135	ORPHA:3216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000218	ORPHA:3216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000369	ORPHA:3216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000377	ORPHA:3216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000384	ORPHA:3216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000396	ORPHA:3216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000402	ORPHA:3216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000405	ORPHA:3216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0000407	ORPHA:3216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0001263	ORPHA:3216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0004299	ORPHA:3216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0004452	ORPHA:3216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3216	Conductive deafness-malformed external ear syndrome		HP:0008551	ORPHA:3216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45	Adenosine monophosphate deaminase deficiency		HP:0003326	ORPHA:45	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45	Adenosine monophosphate deaminase deficiency		HP:0003394	ORPHA:45	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45	Adenosine monophosphate deaminase deficiency		HP:0003690	ORPHA:45	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45	Adenosine monophosphate deaminase deficiency		HP:0003738	ORPHA:45	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45	Adenosine monophosphate deaminase deficiency		HP:0009020	ORPHA:45	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45	Adenosine monophosphate deaminase deficiency	NOT	HP:0002151	ORPHA:45	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:45	Adenosine monophosphate deaminase deficiency	NOT	HP:0008331	ORPHA:45	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0000219	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0000248	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0000252	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0000319	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0000343	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0000369	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0000463	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0001249	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0001250	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0001290	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0001344	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0001999	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0003196	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0005469	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0005487	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0007103	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46	Adenylosuccinate lyase deficiency		HP:0011344	ORPHA:46	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0000162	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0000246	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0000389	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0000407	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0000509	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0000988	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001053	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001287	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001369	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001508	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001596	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001824	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001873	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001875	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001903	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0001945	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002024	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002028	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002088	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002664	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002721	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002754	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002901	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0002960	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0004322	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0004432	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0006532	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0012115	ORPHA:47	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0012378	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0100658	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0100763	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0100765	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0100806	ORPHA:47	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0100838	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47	X-linked agammaglobulinemia		HP:0200042	ORPHA:47	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0001258	ORPHA:401795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0000639	ORPHA:401795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0001762	ORPHA:401795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0002061	ORPHA:401795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0002064	ORPHA:401795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0002169	ORPHA:401795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0002395	ORPHA:401795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0002509	ORPHA:401795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59		HP:0001249	ORPHA:401795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59	NOT	HP:0001317	ORPHA:401795	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:401795	Autosomal recessive spastic paraplegia type 59	NOT	HP:0002500	ORPHA:401795	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:48	Congenital bilateral absence of vas deferens		HP:0003251	ORPHA:48	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48	Congenital bilateral absence of vas deferens		HP:0011962	ORPHA:48	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48	Congenital bilateral absence of vas deferens		HP:0012873	ORPHA:48	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48	Congenital bilateral absence of vas deferens		HP:0000122	ORPHA:48	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48	Congenital bilateral absence of vas deferens		HP:0430121	ORPHA:48	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48	Congenital bilateral absence of vas deferens		HP:0000798	ORPHA:48	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48	Congenital bilateral absence of vas deferens		HP:0012210	ORPHA:48	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41	Dyschromatosis symmetrica hereditaria		HP:0001304	ORPHA:41	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41	Dyschromatosis symmetrica hereditaria		HP:0007988	ORPHA:41	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:41	Dyschromatosis symmetrica hereditaria		HP:0011509	ORPHA:41	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:41	Dyschromatosis symmetrica hereditaria		HP:0012733	ORPHA:41	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001252	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001315	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001410	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001987	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0002013	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0002240	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003215	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003473	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003701	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003738	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0011936	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0030199	ORPHA:42	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0000256	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0000750	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001251	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001254	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001259	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001397	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001640	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001943	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0001946	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0002014	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0002069	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0002373	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0002875	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0002910	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003198	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003202	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003236	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0003394	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0004326	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0005684	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0007185	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0011675	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0012378	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0040155	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42	Medium chain acyl-CoA dehydrogenase deficiency		HP:0045040	ORPHA:42	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000504	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000505	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000572	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000708	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000726	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000752	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0001249	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0001288	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0001328	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0001730	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0001939	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0002311	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0002312	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0002315	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0002385	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0003474	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0004302	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0007018	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0007199	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0008969	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0100543	ORPHA:43	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000011	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000718	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000734	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000846	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0001123	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0001269	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0002381	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0002516	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0002839	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0003154	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0008768	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0011733	ORPHA:43	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000651	ORPHA:43	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0000802	ORPHA:43	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43	X-linked adrenoleukodystrophy		HP:0003470	ORPHA:43	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000174	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000256	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000268	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000358	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000407	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000463	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000486	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000505	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000508	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000639	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000648	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0001250	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0001252	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0001347	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0001392	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0001939	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0002269	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0002353	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0002376	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0004322	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0007598	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000260	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000348	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000431	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0000518	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0007703	ORPHA:44	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0008207	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0011344	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44	Neonatal adrenoleukodystrophy		HP:0100022	ORPHA:44	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000014	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000028	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000052	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000062	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000072	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000126	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000358	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0000800	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0001562	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0001629	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0001631	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0001776	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0002023	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0002089	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0002575	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0003196	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0005280	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0005944	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0006827	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0009800	ORPHA:49	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0010480	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0010945	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0010958	ORPHA:49	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0030261	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0012583	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0012584	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0012620	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0012732	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49	Penile agenesis		HP:0100590	ORPHA:49	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0008066	ORPHA:555905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0031234	ORPHA:555905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0200037	ORPHA:555905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0000989	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0011354	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0012531	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0030057	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0031539	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0100792	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0200035	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0200039	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0200041	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0200097	ORPHA:555905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0001880	ORPHA:555905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0003261	ORPHA:555905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0025528	ORPHA:555905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0031292	ORPHA:555905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0032335	ORPHA:555905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:555905	IgA pemphigus		HP:0100279	ORPHA:555905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000478	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000504	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000935	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000944	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000966	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000975	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0001954	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002652	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002983	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0003016	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0003103	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0003401	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0004322	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0006487	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0008872	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0012332	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0100490	ORPHA:3206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000211	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000632	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000938	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000939	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0001371	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0001376	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0001511	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0001562	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0001762	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002098	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002099	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002104	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002650	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002757	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002857	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0002987	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0006380	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0007328	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0010298	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0012785	ORPHA:3206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000164	ORPHA:3206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000821	ORPHA:3206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0000960	ORPHA:3206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0001252	ORPHA:3206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0006844	ORPHA:3206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0008000	ORPHA:3206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3206	Stüve-Wiedemann syndrome		HP:0100028	ORPHA:3206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0000252	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0000316	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0000347	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0000431	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0000494	ORPHA:3207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0000664	ORPHA:3207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0001181	ORPHA:3207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0001249	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0001252	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0001347	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0002007	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0002119	ORPHA:3207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0002120	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0004322	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0007360	ORPHA:3207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0007370	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3207	White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome		HP:0012430	ORPHA:3207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0006895	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0008872	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0011166	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0011343	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0012817	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0040196	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000076	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000544	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000580	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000618	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000639	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000726	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002421	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002505	ORPHA:3208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000478	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001257	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001270	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001626	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001639	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001712	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001824	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002123	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002333	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002376	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003324	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003388	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003487	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003508	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003510	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003693	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003701	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003756	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0005162	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0006801	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0007083	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0007272	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0007350	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0007663	ORPHA:3208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0000737	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001250	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001251	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001285	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001290	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0001511	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002313	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002359	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0002474	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0003202	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0005150	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3208	Isolated succinate-CoQ reductase deficiency		HP:0006380	ORPHA:3208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0000268	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0000912	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0001156	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0001387	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0002007	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0002650	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0002808	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0003086	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0003300	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0003307	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0003312	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0003498	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0004568	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0005280	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0001382	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0006487	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0008422	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40	Acromesomelic dysplasia, Maroteaux type		HP:0011220	ORPHA:40	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0000277	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0001182	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0001773	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0001831	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0004322	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0004408	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0009882	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0011675	ORPHA:3201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0000176	ORPHA:3201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0000294	ORPHA:3201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0000668	ORPHA:3201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0001373	ORPHA:3201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0002705	ORPHA:3201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0010185	ORPHA:3201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0000162	ORPHA:3201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0000252	ORPHA:3201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0001249	ORPHA:3201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0010044	ORPHA:3201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3201	Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome		HP:0100490	ORPHA:3201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001878	ORPHA:3202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001930	ORPHA:3202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0005502	ORPHA:3202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001081	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001744	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001923	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001972	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001981	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0003281	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0003573	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0011042	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0025435	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0032231	ORPHA:3202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0000969	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001046	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001907	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0002027	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0003265	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0004804	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0005518	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0010972	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0012431	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001900	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0025548	ORPHA:3202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0001901	ORPHA:3202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0030242	ORPHA:3202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3202	Dehydrated hereditary stomatocytosis		HP:0030950	ORPHA:3202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000739	ORPHA:444002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001252	ORPHA:444002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001263	ORPHA:444002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000219	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000286	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000341	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000347	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000358	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000369	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000486	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000508	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000545	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000574	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000722	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000736	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000750	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000753	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000817	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000953	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001028	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001156	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001250	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001256	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001260	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001513	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0001773	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0002079	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0002194	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0002307	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0002421	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0002705	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0004209	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0005280	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0007018	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0007598	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0011368	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0011968	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0012433	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0012448	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0012758	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0030190	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0200034	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0200055	ORPHA:444002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444002	11q22.2q22.3 microdeletion syndrome		HP:0000708	ORPHA:444002	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000750	ORPHA:447997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0001249	ORPHA:447997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0001347	ORPHA:447997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0001252	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0001270	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0001276	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002015	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002061	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002079	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0005484	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0011451	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0012444	ORPHA:447997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000020	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000316	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000369	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000411	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000431	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000664	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000733	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000737	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0000752	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0001999	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002020	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002069	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002169	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002205	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002521	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0002828	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0003739	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0005280	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0006808	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0011471	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0012167	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447997	Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome		HP:0012469	ORPHA:447997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0001878	ORPHA:3203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0001923	ORPHA:3203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0004446	ORPHA:3203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0005502	ORPHA:3203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0025065	ORPHA:3203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0025547	ORPHA:3203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0001046	ORPHA:3203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0001744	ORPHA:3203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0001977	ORPHA:3203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0011273	ORPHA:3203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3203	Overhydrated hereditary stomatocytosis		HP:0025435	ORPHA:3203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0000348	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0000490	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0000616	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0000979	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0001746	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0001872	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0002167	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0003011	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0004322	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0008064	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0001903	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3204	Stormorken-Sjaastad-Langslet syndrome		HP:0001928	ORPHA:3204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001251	ORPHA:94147	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001260	ORPHA:94147	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001310	ORPHA:94147	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001347	ORPHA:94147	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000548	ORPHA:94147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0002015	ORPHA:94147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000572	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000597	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000602	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000639	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001098	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001263	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001268	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001270	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001272	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001319	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001324	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001508	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0001635	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0002059	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0002075	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0002310	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0003474	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0003487	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0007663	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0011968	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0012452	ORPHA:94147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000608	ORPHA:94147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000613	ORPHA:94147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000618	ORPHA:94147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0000709	ORPHA:94147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94147	Spinocerebellar ataxia type 7		HP:0012047	ORPHA:94147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0008245	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0012378	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0012758	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0025483	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0025502	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0031219	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0031507	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0032210	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome	NOT	HP:0000853	ORPHA:99832	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome	NOT	HP:0002925	ORPHA:99832	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome	NOT	HP:0011437	ORPHA:99832	TAS					H	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome	NOT	HP:0030057	ORPHA:99832	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0000707	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0000716	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0000870	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0000958	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0001254	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0001510	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0001609	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0002750	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0005990	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0006579	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99832	Resistance to thyrotropin-releasing hormone syndrome		HP:0008202	ORPHA:99832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0100774	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0200026	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000996	ORPHA:3205	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0001250	ORPHA:3205	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0005306	ORPHA:3205	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000486	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000501	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000648	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000708	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000750	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0001123	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0001249	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0001297	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0001347	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0002315	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0007018	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0012019	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0012222	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0012469	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0012758	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0100659	ORPHA:3205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000212	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000238	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000256	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000364	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000504	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000524	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000541	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000557	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000572	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000610	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000612	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000618	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000689	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0000729	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0001100	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0001131	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0002015	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0002120	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0002204	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0002308	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0002360	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0002514	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0004936	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0007872	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0008046	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0009926	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0011787	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0012377	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0034323	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3205	Sturge-Weber syndrome		HP:0100761	ORPHA:3205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000364	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000504	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001000	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001369	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001373	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001386	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001387	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001717	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0002758	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0002829	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0003355	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0005645	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0007400	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0030764	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0033704	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0100593	ORPHA:56	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000024	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000366	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000787	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001597	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001650	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001654	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0003418	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0004380	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0004382	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0004690	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0007832	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0040319	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0100550	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0100773	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:6000027	ORPHA:56	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000501	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000821	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0000822	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001653	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001658	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001718	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0001878	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0002621	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0002650	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0002659	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0004349	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0004942	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0007906	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0011034	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0011982	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0012119	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0025612	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:0034882	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56	Alkaptonuria		HP:6000025	ORPHA:56	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001945	ORPHA:57	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0012545	ORPHA:57	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001324	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001878	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0003326	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0003458	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0003558	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0003756	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0008331	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0009045	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0100295	ORPHA:57	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0000750	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001249	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001270	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001328	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001510	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0001919	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0002153	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0002913	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0003199	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57	Glycogen storage disease due to aldolase A deficiency		HP:0011675	ORPHA:57	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000256	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001249	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001250	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001257	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001274	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001347	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001355	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001508	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002007	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002017	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002167	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002169	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002353	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002360	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002650	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0007256	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0100729	ORPHA:58	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000496	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000508	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000639	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000651	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000712	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000716	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000975	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001251	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001260	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001288	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001337	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001618	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002015	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002019	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002045	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002381	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002445	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002514	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002615	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002808	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0010535	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0010628	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0100247	ORPHA:58	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000218	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000238	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000470	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000819	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000821	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000822	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000826	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0000938	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001252	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001324	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0001645	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002072	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002093	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002376	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002383	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002410	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0002607	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0003307	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0007481	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0012332	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:58	Alexander disease		HP:0100716	ORPHA:58	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001249	ORPHA:59	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0008936	ORPHA:59	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000275	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000276	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000750	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000767	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000822	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000975	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001251	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001257	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001266	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001332	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001347	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001531	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001649	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001763	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002058	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002205	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002360	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002375	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002751	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002926	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0003202	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0007256	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0008081	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0008872	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0011788	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0012444	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0012448	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0031936	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0045082	ORPHA:59	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000028	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000252	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0000639	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001250	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001319	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001348	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001371	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001558	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002071	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002342	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002421	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002509	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0002510	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0003324	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0003487	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0004322	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0006579	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0011448	ORPHA:59	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001518	ORPHA:59	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001561	ORPHA:59	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0001622	ORPHA:59	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0004488	ORPHA:59	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:59	Allan-Herndon-Dudley syndrome		HP:0100660	ORPHA:59	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000028	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000069	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000100	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000248	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000280	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000307	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000311	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000316	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000322	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000347	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000411	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000486	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000490	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000494	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000563	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000615	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000772	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000822	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0000823	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001131	ORPHA:52	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001256	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001328	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001396	ORPHA:52	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001508	ORPHA:52	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001511	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001629	ORPHA:52	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0001631	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0002007	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0002240	ORPHA:52	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0002750	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0003022	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0003189	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0003298	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0003312	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0003422	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0004209	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0004617	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0004969	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0006571	ORPHA:52	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0008678	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0009882	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0012368	ORPHA:52	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52	Alagille syndrome		HP:0100585	ORPHA:52	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000256	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000944	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0001369	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0001373	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002007	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002653	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002754	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002757	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002758	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0005789	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0005916	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0005930	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0006824	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0007626	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0009882	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0010628	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0010885	ORPHA:53	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000164	ORPHA:53	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000648	ORPHA:53	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0001903	ORPHA:53	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002650	ORPHA:53	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002857	ORPHA:53	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0004322	ORPHA:53	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0012378	ORPHA:53	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000238	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000365	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000618	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000670	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0001873	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0001881	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0002901	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0005746	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0012145	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0030757	ORPHA:53	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0000505	ORPHA:53	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53	Albers-Schönberg osteopetrosis		HP:0001293	ORPHA:53	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0000483	ORPHA:54	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0000486	ORPHA:54	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0000505	ORPHA:54	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0000545	ORPHA:54	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0000613	ORPHA:54	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0000615	ORPHA:54	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0000639	ORPHA:54	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0001103	ORPHA:54	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0001107	ORPHA:54	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0001480	ORPHA:54	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0005592	ORPHA:54	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0007730	ORPHA:54	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0007750	ORPHA:54	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54	X-linked recessive ocular albinism		HP:0008069	ORPHA:54	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1490	Corneal dystrophy-perceptive deafness syndrome		HP:0000407	ORPHA:1490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1490	Corneal dystrophy-perceptive deafness syndrome		HP:0000505	ORPHA:1490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1490	Corneal dystrophy-perceptive deafness syndrome		HP:0000639	ORPHA:1490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1490	Corneal dystrophy-perceptive deafness syndrome		HP:0001131	ORPHA:1490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1490	Corneal dystrophy-perceptive deafness syndrome		HP:0007957	ORPHA:1490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1497	X-linked complicated corpus callosum dysgenesis		HP:0000252	ORPHA:1497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1497	X-linked complicated corpus callosum dysgenesis		HP:0001249	ORPHA:1497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1497	X-linked complicated corpus callosum dysgenesis		HP:0001250	ORPHA:1497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1497	X-linked complicated corpus callosum dysgenesis		HP:0001257	ORPHA:1497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1497	X-linked complicated corpus callosum dysgenesis		HP:0001321	ORPHA:1497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1497	X-linked complicated corpus callosum dysgenesis		HP:0001324	ORPHA:1497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1497	X-linked complicated corpus callosum dysgenesis		HP:0002251	ORPHA:1497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0000252	ORPHA:1496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0000262	ORPHA:1496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0000486	ORPHA:1496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0000545	ORPHA:1496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0000639	ORPHA:1496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0001249	ORPHA:1496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0001250	ORPHA:1496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0001263	ORPHA:1496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0001274	ORPHA:1496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0001363	ORPHA:1496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0002353	ORPHA:1496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0002410	ORPHA:1496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0004374	ORPHA:1496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1496	Corpus callosum agenesis-neuronopathy syndrome		HP:0007703	ORPHA:1496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001873	ORPHA:99827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001945	ORPHA:99827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0003496	ORPHA:99827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0030005	ORPHA:99827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000421	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002014	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002017	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002027	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002039	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002240	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002315	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0003236	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0003237	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0003326	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0003645	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0020071	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0025258	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0025435	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0030833	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0032198	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0200026	ORPHA:99827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000225	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000509	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000613	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000707	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000712	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000713	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000790	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000822	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000952	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000975	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000979	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001259	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001262	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001289	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001399	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001649	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001662	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001744	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001882	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001974	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002105	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002248	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002249	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002321	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002380	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002615	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002716	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0025143	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0031364	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0100247	ORPHA:99827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000031	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000093	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000573	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0000846	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001082	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001541	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001698	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001735	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0001876	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002092	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0002829	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0005162	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0007420	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0011029	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0011710	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0011850	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0011854	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0011896	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0011897	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0012151	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0012219	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0012282	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0012819	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0025420	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0031218	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0100309	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99827	Crimean-Congo hemorrhagic fever		HP:0100796	ORPHA:99827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000252	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000384	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000411	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0001276	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0001510	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0002079	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0002119	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0002750	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0006532	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0010864	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0010978	ORPHA:1495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000174	ORPHA:1495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000347	ORPHA:1495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0001511	ORPHA:1495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0001522	ORPHA:1495	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0001883	ORPHA:1495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0100490	ORPHA:1495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000160	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000348	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000639	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0000648	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0001250	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0001608	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0002020	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0003196	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0004322	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1495	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome		HP:0030680	ORPHA:1495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0000225	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0000421	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0000967	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0000978	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0000988	ORPHA:99828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0000989	ORPHA:99828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0001254	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0001342	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0001541	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0001873	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0001882	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0001945	ORPHA:99828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002014	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002017	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002027	ORPHA:99828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002239	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002240	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002315	ORPHA:99828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002615	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0002829	ORPHA:99828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0003075	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99828	Dengue fever		HP:0006543	ORPHA:99828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001945	ORPHA:99829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002018	ORPHA:99829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0003496	ORPHA:99829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0020071	ORPHA:99829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0031964	ORPHA:99829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0000083	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001662	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001892	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001919	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001942	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002013	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002027	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002248	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002315	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002829	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0003236	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0003259	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0003326	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0006277	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0025143	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0030139	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0030783	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0031956	ORPHA:99829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0000952	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001250	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001259	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001735	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001873	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0001974	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002014	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002904	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0003225	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0003419	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0005115	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0008151	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0011897	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0011900	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0030005	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0031273	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0032066	ORPHA:99829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0000988	ORPHA:99829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002133	ORPHA:99829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0002516	ORPHA:99829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0011029	ORPHA:99829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0012664	ORPHA:99829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0031690	ORPHA:99829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99829	Yellow fever		HP:0100519	ORPHA:99829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001010	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001249	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001252	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001263	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001274	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001522	ORPHA:1493	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001638	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0002205	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0002353	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0002719	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0004322	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0005374	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0005999	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0007703	ORPHA:1493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000218	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000437	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000518	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000639	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000648	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001250	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001321	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001947	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0002282	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0012110	ORPHA:1493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000316	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000407	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0000601	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001103	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0001387	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0002120	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0002360	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0004315	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0008348	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0008872	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1493	Vici syndrome		HP:0011968	ORPHA:1493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0001945	ORPHA:99824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0003496	ORPHA:99824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0005268	ORPHA:99824	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0020071	ORPHA:99824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0025406	ORPHA:99824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0400008	ORPHA:99824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0001324	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0002015	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0002017	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0002027	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0002315	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0012735	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0025439	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0100749	ORPHA:99824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0000282	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0000365	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0000509	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0000952	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0001250	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0001622	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0001892	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0002014	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0002094	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0002829	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0003418	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0031273	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0100520	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99824	Lassa fever		HP:0100806	ORPHA:99824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000175	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000204	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000252	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000322	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000411	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000541	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000567	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000568	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000588	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000639	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000648	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000823	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000826	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000892	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000902	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0000921	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001000	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001012	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001252	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001257	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001276	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001302	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001338	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001357	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0001385	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002019	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002020	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002024	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002036	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002119	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002126	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002342	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002353	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002650	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0002884	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0003305	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0003316	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0004374	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0005338	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0005815	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0007360	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0007703	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0008872	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0010759	ORPHA:50	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0010864	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0011343	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0011344	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0012469	ORPHA:50	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0200008	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50	Aicardi syndrome		HP:0200055	ORPHA:50	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0000751	ORPHA:99825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0001250	ORPHA:99825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0001259	ORPHA:99825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0001336	ORPHA:99825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0001337	ORPHA:99825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0001945	ORPHA:99825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0002017	ORPHA:99825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0002039	ORPHA:99825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0002098	ORPHA:99825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0002315	ORPHA:99825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0002321	ORPHA:99825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0002383	ORPHA:99825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0002615	ORPHA:99825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0003326	ORPHA:99825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0012378	ORPHA:99825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0012735	ORPHA:99825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99825	Nipah virus disease		HP:0100776	ORPHA:99825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001257	ORPHA:51	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001263	ORPHA:51	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001276	ORPHA:51	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002132	ORPHA:51	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002139	ORPHA:51	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002187	ORPHA:51	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0007052	ORPHA:51	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000252	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000625	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000737	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000958	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001250	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001332	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001433	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001955	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002071	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002079	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002119	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001288	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002371	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002376	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002415	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002514	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002910	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002960	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000444	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0004322	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0004374	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0007076	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0008936	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0009704	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0009709	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0009710	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0012444	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0030356	ORPHA:51	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000054	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000369	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000496	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000501	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000508	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000639	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000819	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000821	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0000965	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001063	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001087	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001337	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001357	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001369	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001609	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001640	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002313	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002315	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002510	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002650	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0002828	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0003552	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0004809	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0006579	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0007108	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0007256	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0012490	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0030880	ORPHA:51	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0001639	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0004942	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0004963	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0005550	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0011834	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0030038	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0040140	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0100578	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51	Aicardi-Goutières syndrome		HP:0100614	ORPHA:51	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002716	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002829	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002900	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002910	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003073	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003128	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003236	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003256	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003259	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003418	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003645	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0008151	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0011029	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0011151	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0011896	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0012534	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0025085	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0030139	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0031246	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0031273	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0040186	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0410288	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000554	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000709	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001882	ORPHA:99826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001888	ORPHA:99826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0010702	ORPHA:99826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0020071	ORPHA:99826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0030005	ORPHA:99826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001892	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001923	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001945	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002013	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002014	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002027	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002039	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002315	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0003326	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0004332	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0012137	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0025143	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0030953	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0032043	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0032169	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0410257	ORPHA:99826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000083	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000718	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000967	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000978	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000988	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001250	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001254	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001259	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001289	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001649	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001662	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001873	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001943	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001944	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002018	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002045	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002329	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002615	ORPHA:99826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0000952	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001369	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001701	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001733	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0001987	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0002480	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0004360	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0005521	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0011024	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0011106	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99826	Marburg hemorrhagic fever		HP:0100796	ORPHA:99826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001639	ORPHA:444013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0003128	ORPHA:444013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0000707	ORPHA:444013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0008947	ORPHA:444013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0000505	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0000961	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001250	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001256	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001263	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001508	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001635	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001667	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001712	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0001716	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0002415	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0002878	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0003388	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0008347	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0008872	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0010307	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0011923	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0012666	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0012696	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0012747	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0012751	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0012763	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444013	Combined oxidative phosphorylation defect type 23		HP:0100543	ORPHA:444013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0000978	ORPHA:177926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0003125	ORPHA:177926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0000132	ORPHA:177926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0000421	ORPHA:177926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0001892	ORPHA:177926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0004846	ORPHA:177926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0006298	ORPHA:177926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0011890	ORPHA:177926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0011891	ORPHA:177926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0003645	ORPHA:177926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0005261	ORPHA:177926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177926	Bleeding disorder in hemophilia A carriers		HP:0007420	ORPHA:177926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000248	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000272	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000358	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000370	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000405	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000413	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000463	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000486	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000772	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000776	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0000921	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0001249	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0001252	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0001537	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0001545	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0001629	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0002007	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0002093	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0002650	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0003272	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0004322	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0004349	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0001382	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0007477	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0009623	ORPHA:1488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1488	Cooper-Jabs syndrome		HP:0100490	ORPHA:1488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0001156	ORPHA:1487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0001171	ORPHA:1487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0001199	ORPHA:1487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0001810	ORPHA:1487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0008388	ORPHA:1487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0008391	ORPHA:1487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0010624	ORPHA:1487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1487	Cooks syndrome		HP:0011304	ORPHA:1487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0001892	ORPHA:329971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0001903	ORPHA:329971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0002573	ORPHA:329971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0001017	ORPHA:329971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0001510	ORPHA:329971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0000969	ORPHA:329971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0005227	ORPHA:329971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0004394	ORPHA:329971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0030256	ORPHA:329971	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0100896	ORPHA:329971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329971	Generalized juvenile polyposis/juvenile polyposis coli		HP:0004783	ORPHA:329971	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0000316	ORPHA:1486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0000347	ORPHA:1486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0000358	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0000465	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0000470	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0000772	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0001376	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0001561	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0002089	ORPHA:1486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0002757	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0003100	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0003103	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0003202	ORPHA:1486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0003272	ORPHA:1486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0003312	ORPHA:1486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0004322	ORPHA:1486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0009775	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1486	Lethal congenital contracture syndrome type 1		HP:0009811	ORPHA:1486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0000175	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0000632	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0000966	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0001263	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0001376	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0002804	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0100335	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1484	Contractures-ectodermal dysplasia-cleft lip/palate syndrome		HP:0100543	ORPHA:1484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477781	Primary condylar hyperplasia		HP:3000077	ORPHA:477781	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477781	Primary condylar hyperplasia		HP:0000306	ORPHA:477781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477781	Primary condylar hyperplasia		HP:0000324	ORPHA:477781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477781	Primary condylar hyperplasia		HP:0009102	ORPHA:477781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477781	Primary condylar hyperplasia		HP:0010754	ORPHA:477781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477781	Primary condylar hyperplasia		HP:0001572	ORPHA:477781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0000958	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0000988	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0000989	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0000992	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001029	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001252	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001260	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001324	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001369	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001376	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001596	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001609	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001618	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001638	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001681	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001701	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001824	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0001945	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002015	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002019	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002027	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002091	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002094	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002206	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002239	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002633	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002829	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0002960	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0003236	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0003326	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0003394	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0003457	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0003565	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0003761	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0010783	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0011227	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0011675	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0011710	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0012378	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0012735	ORPHA:93672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0100540	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0100579	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0100585	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0100614	ORPHA:93672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93672	Juvenile dermatomyositis		HP:0200042	ORPHA:93672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0000365	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0000529	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0001249	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0001263	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002123	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002133	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002151	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002273	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002376	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002500	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002506	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0003200	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0008347	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0011923	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0011924	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0031165	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0200134	ORPHA:477774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0000729	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0001344	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0001790	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002015	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0002079	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0004305	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0007351	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0010853	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0012531	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0025517	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0040288	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477774	Combined oxidative phosphorylation defect type 27		HP:0100275	ORPHA:477774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329967	Intermittent hydrarthrosis		HP:0001386	ORPHA:329967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329967	Intermittent hydrarthrosis		HP:0002829	ORPHA:329967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329967	Intermittent hydrarthrosis		HP:0002815	ORPHA:329967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329967	Intermittent hydrarthrosis		HP:0045086	ORPHA:329967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329967	Intermittent hydrarthrosis		HP:0000934	ORPHA:329967	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0001631	ORPHA:1478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0001684	ORPHA:1478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0005110	ORPHA:1478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0031664	ORPHA:1478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0001635	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0001640	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0001962	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0002092	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0002205	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0002875	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0004749	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0005133	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0010445	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0011567	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0011712	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0012378	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0033567	ORPHA:1478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0001297	ORPHA:1478	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1478	Interatrial communication		HP:0031297	ORPHA:1478	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000003	ORPHA:1475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000076	ORPHA:1475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000083	ORPHA:1475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000089	ORPHA:1475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000110	ORPHA:1475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000365	ORPHA:1475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000480	ORPHA:1475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000486	ORPHA:1475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000505	ORPHA:1475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000545	ORPHA:1475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000588	ORPHA:1475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0000639	ORPHA:1475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0001093	ORPHA:1475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1475	Renal coloboma syndrome		HP:0001382	ORPHA:1475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000407	ORPHA:1473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000486	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000501	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000505	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000508	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000518	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000541	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000567	ORPHA:1473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000568	ORPHA:1473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000612	ORPHA:1473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000627	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000639	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000648	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0000790	ORPHA:1473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0001249	ORPHA:1473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0100337	ORPHA:1473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1473	Uveal coloboma-cleft lip and palate-intellectual disability		HP:0007957	ORPHA:1473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0000104	ORPHA:1471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0000567	ORPHA:1471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0001817	ORPHA:1471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0004322	ORPHA:1471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0005831	ORPHA:1471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0009882	ORPHA:1471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0011304	ORPHA:1471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0100490	ORPHA:1471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1471	Coloboma of macula-brachydactyly type B syndrome		HP:0100798	ORPHA:1471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1479	Atrial septal defect-atrioventricular conduction defects syndrome		HP:0001671	ORPHA:1479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1479	Atrial septal defect-atrioventricular conduction defects syndrome		HP:0011675	ORPHA:1479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1479	Atrial septal defect-atrioventricular conduction defects syndrome		HP:0011710	ORPHA:1479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0012412	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0012650	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0025160	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0030339	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0031507	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0100716	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0200055	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000938	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000939	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001250	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001256	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001263	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001385	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001518	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001558	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001999	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002342	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002578	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002714	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002870	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002871	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0006889	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0010741	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0010829	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0031100	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0031169	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0100739	ORPHA:177904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000826	ORPHA:177904	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000028	ORPHA:177904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001513	ORPHA:177904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002119	ORPHA:177904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002591	ORPHA:177904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0008872	ORPHA:177904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000044	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000046	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000060	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000064	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000486	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000504	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000708	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000709	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000717	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000729	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000786	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000789	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000819	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000823	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0000824	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001010	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001252	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001328	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001508	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0001773	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002205	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002360	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0002650	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0003241	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0004322	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0005599	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0007730	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0007874	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0008734	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0008770	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0009088	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0010627	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0011734	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0011787	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0012104	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0012105	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0012166	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177904	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2		HP:0012411	ORPHA:177904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000028	ORPHA:177901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001513	ORPHA:177901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002119	ORPHA:177901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0008872	ORPHA:177901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000044	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000046	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000060	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000064	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000486	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000504	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000708	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000709	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000717	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000729	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000786	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000789	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000819	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000823	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000824	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001010	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001252	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001263	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001328	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001508	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001773	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002205	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002342	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002360	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002591	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002650	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0003241	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0004322	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0005599	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0007730	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0007874	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0008734	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0008770	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0009088	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0010627	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0011734	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0011787	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0012104	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0012105	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0012166	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0012411	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0012412	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0012650	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0025160	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0030339	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0031507	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0100716	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0100739	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0200055	ORPHA:177901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000219	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000938	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000939	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001250	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001256	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001385	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001518	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0001558	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002578	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002714	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002870	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0002871	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0006889	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0010741	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0010829	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0031100	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0031169	ORPHA:177901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177901	Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1		HP:0000826	ORPHA:177901	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0000303	ORPHA:2790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0000407	ORPHA:2790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0000639	ORPHA:2790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0000772	ORPHA:2790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0003103	ORPHA:2790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0003312	ORPHA:2790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0004493	ORPHA:2790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0005019	ORPHA:2790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0005789	ORPHA:2790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0010628	ORPHA:2790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0100789	ORPHA:2790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0100861	ORPHA:2790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2790	Endosteal hyperostosis, Worth type		HP:0100923	ORPHA:2790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0001896	ORPHA:300298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0001903	ORPHA:300298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0003281	ORPHA:300298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0012464	ORPHA:300298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0000027	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0000135	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0000864	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0000980	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0002910	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0003452	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0004823	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0012378	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0012465	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0025066	ORPHA:300298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0000821	ORPHA:300298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0000846	ORPHA:300298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0000957	ORPHA:300298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0001433	ORPHA:300298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0001510	ORPHA:300298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300298	Severe congenital hypochromic anemia with ringed sideroblasts		HP:0012134	ORPHA:300298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0000360	ORPHA:1467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0000491	ORPHA:1467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0000613	ORPHA:1467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0001751	ORPHA:1467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0002321	ORPHA:1467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0007663	ORPHA:1467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0000407	ORPHA:1467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0001894	ORPHA:1467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0001903	ORPHA:1467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0001974	ORPHA:1467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0003565	ORPHA:1467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0100533	ORPHA:1467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0000509	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0000554	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0000618	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0001659	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0002633	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0005310	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0100532	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1467	Cogan syndrome		HP:0100534	ORPHA:1467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000135	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000232	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000252	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000347	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000407	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000431	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000470	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000505	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000518	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000568	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000648	ORPHA:1466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0000992	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001250	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001252	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001276	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001315	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001387	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001511	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001522	ORPHA:1466	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0001883	ORPHA:1466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0002120	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0002514	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0002804	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0004322	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0005105	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0005487	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0007360	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0007703	ORPHA:1466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0008872	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0009830	ORPHA:1466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0010978	ORPHA:1466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0011344	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1466	COFS syndrome		HP:0100490	ORPHA:1466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000154	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000179	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000280	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000574	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000998	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001792	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0011231	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0011968	ORPHA:1465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000028	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000119	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000219	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000289	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000294	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000365	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000455	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000463	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000486	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000505	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000508	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000684	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000708	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001007	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001250	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001382	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001510	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001627	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001999	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002209	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002342	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002650	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002719	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002750	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002788	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0003196	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0005280	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0008398	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0008897	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0008947	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0009237	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0009928	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0010864	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0011937	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0011951	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0012810	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0030084	ORPHA:1465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000047	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000085	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000545	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000718	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000729	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000752	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001274	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001305	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001344	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001629	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001631	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001636	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001643	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0009879	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0012523	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0100790	ORPHA:1465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0000252	ORPHA:1465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0001511	ORPHA:1465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002884	ORPHA:1465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1465	Coffin-Siris syndrome		HP:0002895	ORPHA:1465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0030950	ORPHA:1464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0034350	ORPHA:1464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0001508	ORPHA:1464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0001635	ORPHA:1464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0002098	ORPHA:1464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0002789	ORPHA:1464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0004383	ORPHA:1464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0030148	ORPHA:1464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0000961	ORPHA:1464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0001640	ORPHA:1464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0002040	ORPHA:1464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0002240	ORPHA:1464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0011675	ORPHA:1464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1464	Univentricular heart		HP:0012418	ORPHA:1464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0000961	ORPHA:1461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0030680	ORPHA:1461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0001629	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0001633	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0001642	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0001669	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0001718	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0002093	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0004381	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0010446	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0011968	ORPHA:1461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0000765	ORPHA:1461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1461	Criss-cross heart		HP:0001999	ORPHA:1461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0001249	ORPHA:324262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0001347	ORPHA:324262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0002066	ORPHA:324262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0003698	ORPHA:324262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0000565	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0000571	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0001310	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0002075	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0002167	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0002406	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0004302	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0011347	ORPHA:324262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0000508	ORPHA:324262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0001250	ORPHA:324262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0001271	ORPHA:324262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0001344	ORPHA:324262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324262	Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency		HP:0007979	ORPHA:324262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000408	ORPHA:2791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000670	ORPHA:2791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0006479	ORPHA:2791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0011070	ORPHA:2791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0011078	ORPHA:2791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000212	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000276	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000293	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000326	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000343	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000463	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000679	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000682	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000684	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000704	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0001757	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0003771	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0011051	ORPHA:2791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000480	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000482	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000518	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000568	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0000612	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0011068	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0031353	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2791	Otodental syndrome		HP:0100719	ORPHA:2791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000218	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000293	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000324	ORPHA:2792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000400	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000405	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000411	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000413	ORPHA:2792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000463	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0000889	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0001249	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0001263	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0001276	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0001347	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0002167	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0002750	ORPHA:2792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0003691	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0004322	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0004467	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0005280	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0007477	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0008678	ORPHA:2792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0009738	ORPHA:2792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2792	Otofaciocervical syndrome		HP:0200021	ORPHA:2792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0000268	ORPHA:2793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0000400	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0000582	ORPHA:2793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0000940	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0001256	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0001371	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0001597	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0006380	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0008577	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0009738	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0009756	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0009906	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2793	Otoonychoperoneal syndrome		HP:0011039	ORPHA:2793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0012119	ORPHA:464453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0000739	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0000961	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0001289	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0001941	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0001962	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0002013	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0002094	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0002315	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0002321	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0012378	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0012418	ORPHA:464453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0001259	ORPHA:464453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0001279	ORPHA:464453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0001649	ORPHA:464453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0002027	ORPHA:464453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0002329	ORPHA:464453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0007185	ORPHA:464453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0011675	ORPHA:464453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0001250	ORPHA:464453	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464453	Acquired methemoglobinemia		HP:0002098	ORPHA:464453	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000147	ORPHA:2795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000795	ORPHA:2795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0003457	ORPHA:2795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0100518	ORPHA:2795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000016	ORPHA:2795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000876	ORPHA:2795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0001007	ORPHA:2795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0001061	ORPHA:2795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000020	ORPHA:2795	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000132	ORPHA:2795	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000137	ORPHA:2795	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2795	Fowler urethral sphincter dysfunction syndrome		HP:0000141	ORPHA:2795	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000280	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000508	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000771	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000845	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000939	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000969	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000975	ORPHA:2796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000964	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0000982	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001051	ORPHA:2796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001061	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001072	ORPHA:2796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001231	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001369	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001376	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001386	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001744	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0001903	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002024	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002239	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002240	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002650	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002653	ORPHA:2796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002754	ORPHA:2796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002797	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002829	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0002970	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0003103	ORPHA:2796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0004398	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0005561	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0005930	ORPHA:2796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0008069	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0010541	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0010720	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0010829	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0010885	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0011362	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0100021	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0100526	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0100760	ORPHA:2796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2796	Pachydermoperiostosis		HP:0200055	ORPHA:2796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2798	Pachygyria-intellectual disability-epilepsy syndrome		HP:0001250	ORPHA:2798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2798	Pachygyria-intellectual disability-epilepsy syndrome		HP:0001263	ORPHA:2798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2798	Pachygyria-intellectual disability-epilepsy syndrome		HP:0001622	ORPHA:2798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2798	Pachygyria-intellectual disability-epilepsy syndrome		HP:0010864	ORPHA:2798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0000708	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0001263	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0001319	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0001513	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0001558	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0001773	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0001999	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0002591	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0004322	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0008872	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0200055	ORPHA:177910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0004039	ORPHA:177910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0004283	ORPHA:177910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0000044	ORPHA:177910	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0001010	ORPHA:177910	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0003241	ORPHA:177910	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0005599	ORPHA:177910	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:177910	Prader-Willi syndrome due to imprinting mutation		HP:0007730	ORPHA:177910	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0010818	ORPHA:505652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000232	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000337	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000490	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000729	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000750	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000817	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0001249	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0001252	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0001288	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0001510	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002002	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002019	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002020	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002069	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002194	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0001288	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002421	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002521	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0003763	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0003808	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0006979	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0007328	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0007359	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0009852	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0010841	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0011220	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0011343	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0011344	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0011471	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0011968	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0012171	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0012469	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0012471	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0032794	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0033850	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0100704	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:5200061	ORPHA:505652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000252	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000341	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000348	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000565	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000577	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000664	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0000749	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0001332	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0001822	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002072	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002104	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002650	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002783	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002808	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505652	CDKL5-deficiency disorder		HP:0002883	ORPHA:505652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0000253	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001118	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001249	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001250	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001263	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001285	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001510	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001999	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0004322	ORPHA:438178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0000219	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0000316	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0000319	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0000343	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0000400	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0000508	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001272	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0001305	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0002540	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0002553	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0003196	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0003698	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		HP:0005280	ORPHA:438178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0000939	ORPHA:2788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0002659	ORPHA:2788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0000541	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0000938	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0001141	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0001382	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0002505	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0002515	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0003016	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0004327	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0006367	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0007875	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0007898	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0007957	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0008947	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0012052	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0012109	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0030490	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0040069	ORPHA:2788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0000568	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0000750	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0001263	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0002007	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0002194	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0002645	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0003366	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0004322	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0006934	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0030551	ORPHA:2788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0000384	ORPHA:2788	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0000592	ORPHA:2788	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0008236	ORPHA:2788	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0030515	ORPHA:2788	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2788	Osteoporosis-pseudoglioma syndrome		HP:0030680	ORPHA:2788	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000268	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000272	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000275	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000347	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000358	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000369	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000405	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000413	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000494	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000508	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0002435	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0002645	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0002705	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0100775	ORPHA:2789	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000023	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000319	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000470	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000678	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000767	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0001537	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0002162	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0002650	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0003312	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0004452	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0004493	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0005487	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0001382	ORPHA:2789	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000028	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000218	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000286	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000316	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000407	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000520	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0000612	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0001252	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0001263	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0001629	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0002308	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0002808	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0003307	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2789	Lateral meningocele syndrome		HP:0003396	ORPHA:2789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000003	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000023	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000083	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000112	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000202	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000238	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000256	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000276	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000369	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000426	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000463	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000486	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000505	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000508	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000567	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000588	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000612	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000639	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000657	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0000864	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001162	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001250	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001251	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001252	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001288	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001320	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001337	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001347	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001394	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001409	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0001744	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002085	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002104	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002240	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002269	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002342	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002553	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002612	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002650	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002793	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002896	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0002910	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0004422	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0005248	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0007360	ORPHA:1454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0007370	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0008872	ORPHA:1454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1454	Joubert syndrome with hepatic defect		HP:0100626	ORPHA:1454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1453	Cleidorhizomelic syndrome		HP:0000889	ORPHA:1453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1453	Cleidorhizomelic syndrome		HP:0001156	ORPHA:1453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1453	Cleidorhizomelic syndrome		HP:0004209	ORPHA:1453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1453	Cleidorhizomelic syndrome		HP:0004220	ORPHA:1453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1453	Cleidorhizomelic syndrome		HP:0005019	ORPHA:1453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1453	Cleidorhizomelic syndrome		HP:0007598	ORPHA:1453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1453	Cleidorhizomelic syndrome		HP:0008905	ORPHA:1453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000389	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000684	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000772	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000939	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0001156	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000164	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000239	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000316	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000340	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000347	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000670	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000682	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000774	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000894	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002007	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002205	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002645	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002652	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002705	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0004322	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0008821	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0010669	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0011069	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0200021	ORPHA:1452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000246	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000303	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000364	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000365	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0003298	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0004331	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0005107	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0005280	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0005916	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0010751	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0010807	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0011219	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0011800	ORPHA:1452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000162	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000175	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000248	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000256	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000337	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0000882	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0001172	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0001182	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0001810	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002644	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002650	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002757	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002812	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0002857	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0004209	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0005930	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0008391	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1452	Cleidocranial dysplasia		HP:0010535	ORPHA:1452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000256	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000365	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000407	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000505	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000520	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000538	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000554	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000618	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000969	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0000979	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001025	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001156	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001249	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001263	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001287	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001367	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001373	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001476	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001510	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001622	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001744	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001872	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001874	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001903	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001911	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001945	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0001974	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002007	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002017	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002076	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002240	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002353	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002516	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002652	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002716	ORPHA:1451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0002829	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0003326	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0003565	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0004349	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0011227	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0012378	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0100533	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0100654	ORPHA:1451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1451	CINCA syndrome		HP:0200034	ORPHA:1451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0000069	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0000126	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0000174	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0000286	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0000340	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0000348	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0000463	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0001249	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0001561	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0002007	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0002162	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0003196	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0004097	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1450	Ring chromosome 8 syndrome		HP:0100830	ORPHA:1450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0001263	ORPHA:79350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0002342	ORPHA:79350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0008897	ORPHA:79350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0011968	ORPHA:79350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0012279	ORPHA:79350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0000047	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0000154	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0000252	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0000293	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0000337	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0000341	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0000347	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0001276	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0001999	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0002020	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0002069	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0100540	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79350	3-phosphoserine phosphatase deficiency, infantile/juvenile form		HP:0100633	ORPHA:79350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000944	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0002684	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0005465	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0008808	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0008818	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0011001	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0011002	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0100670	ORPHA:2780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000175	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000176	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000193	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000239	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000256	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000270	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000405	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000431	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000684	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0002007	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0002650	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0002705	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0005469	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0011220	ORPHA:2780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000248	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000278	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000286	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000347	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000358	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000369	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0000518	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0001249	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0001263	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0001328	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0001555	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0001650	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0001680	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0002300	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0002381	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0002514	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0003298	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0003307	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0003510	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0010529	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0010628	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2780	Osteopathia striata-cranial sclerosis syndrome		HP:0012368	ORPHA:2780	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0012277	ORPHA:79351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0012279	ORPHA:79351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0000252	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0000565	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001257	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001508	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001511	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002013	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0004322	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0006808	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0007281	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0011097	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0011344	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0011451	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0011968	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0012448	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0012762	ORPHA:79351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0000023	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0000135	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0000519	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0000708	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0000737	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001181	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001276	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0006872	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001537	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001889	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0001999	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002020	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002069	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002079	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002119	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002121	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002123	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002305	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002510	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0002536	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0006872	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0007503	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0010719	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0010819	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0010821	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0011343	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0030215	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0100633	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79351	3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form		HP:0100704	ORPHA:79351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0012048	ORPHA:464440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0012049	ORPHA:464440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0002345	ORPHA:464440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0002356	ORPHA:464440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0002451	ORPHA:464440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0002530	ORPHA:464440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0004373	ORPHA:464440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464440	Primary dystonia, DYT27 type		HP:0007351	ORPHA:464440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001513	ORPHA:177907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001612	ORPHA:177907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0002033	ORPHA:177907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0008872	ORPHA:177907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000044	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000219	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000341	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000824	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001256	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001319	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001773	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001999	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0002098	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0002205	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0002714	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0003241	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0004322	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0006829	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0007874	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0010627	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0025160	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0200055	ORPHA:177907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000077	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000154	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000175	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000193	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000218	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000232	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000252	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000278	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000316	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000347	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000384	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000446	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000448	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000455	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000463	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000470	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000486	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000490	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000520	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000540	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000545	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000582	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000601	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000670	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000708	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000722	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000733	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0012760	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000739	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000750	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0000953	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001010	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001156	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001250	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001263	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001265	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001344	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001347	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001511	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001562	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001611	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001627	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001643	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001655	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001763	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001776	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0001845	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0002120	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0002650	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0003196	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0004209	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0005469	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0005599	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0006347	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0006956	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0007018	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0007730	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0009085	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0010801	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0010864	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0011470	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0012166	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0012168	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0012433	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0012704	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0012775	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0030084	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0040025	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0040082	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0100704	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177907	Prader-Willi syndrome due to translocation		HP:0200096	ORPHA:177907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231080	High-grade dysplasia in patients with Barrett esophagus		HP:0100580	ORPHA:231080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231080	High-grade dysplasia in patients with Barrett esophagus		HP:0002015	ORPHA:231080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231080	High-grade dysplasia in patients with Barrett esophagus		HP:0002020	ORPHA:231080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231080	High-grade dysplasia in patients with Barrett esophagus		HP:0005240	ORPHA:231080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001947	ORPHA:2785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0011002	ORPHA:2785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0012379	ORPHA:2785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000164	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001263	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001293	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001999	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002049	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002135	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002514	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002757	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002901	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0003148	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0003236	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0004322	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0008341	ORPHA:2785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000126	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000160	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000179	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000218	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000248	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000278	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000347	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000400	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000479	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000592	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000648	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000692	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000767	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000787	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000867	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001105	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001249	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001328	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001357	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001508	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001562	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001873	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001876	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001882	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001903	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002240	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002518	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002684	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0004445	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0005461	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0005528	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0006335	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0006641	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0006824	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0010864	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0011220	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0012370	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0030812	ORPHA:2785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0000405	ORPHA:2785	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0001942	ORPHA:2785	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002092	ORPHA:2785	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002273	ORPHA:2785	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0002870	ORPHA:2785	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2785	Osteopetrosis with renal tubular acidosis		HP:0012181	ORPHA:2785	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000072	ORPHA:1458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000286	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000396	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000407	ORPHA:1458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000463	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000486	ORPHA:1458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000508	ORPHA:1458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000518	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000639	ORPHA:1458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000682	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0000684	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0001156	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0001252	ORPHA:1458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0001263	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0001374	ORPHA:1458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0001600	ORPHA:1458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0001629	ORPHA:1458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0002644	ORPHA:1458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0002650	ORPHA:1458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0002750	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0003196	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0003312	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0003417	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0004122	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0004322	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0005242	ORPHA:1458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0005280	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0001382	ORPHA:1458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0005930	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0006482	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0009901	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0010049	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1458	CODAS syndrome		HP:0012368	ORPHA:1458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0000479	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0000505	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0000545	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0000639	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0000926	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0000939	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0000980	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0001010	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0001022	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0002808	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0004322	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2786	Osteoporosis-oculocutaneous hypopigmentation syndrome		HP:0005599	ORPHA:2786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0012305	ORPHA:1457	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0011103	ORPHA:1457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0001640	ORPHA:1457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0001647	ORPHA:1457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0001677	ORPHA:1457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0004383	ORPHA:1457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0000822	ORPHA:1457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0001635	ORPHA:1457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0001643	ORPHA:1457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0005301	ORPHA:1457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0011682	ORPHA:1457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0012304	ORPHA:1457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0001297	ORPHA:1457	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0001636	ORPHA:1457	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0002092	ORPHA:1457	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation		HP:0010883	ORPHA:1457	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation	NOT	HP:0005295	ORPHA:1457	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1457	Aorta coarctation	NOT	HP:0011611	ORPHA:1457	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0000118	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0000837	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0008669	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0008734	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0011961	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0012205	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0012864	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399808	Male infertility with teratozoospermia due to single gene mutation		HP:0012868	ORPHA:399808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0004348	ORPHA:210110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0002659	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0002757	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0003418	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0004618	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0004975	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0005652	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0005746	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0005789	ORPHA:210110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0000707	ORPHA:210110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0001903	ORPHA:210110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0003155	ORPHA:210110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0000164	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0000505	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0000689	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0001293	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0001433	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0002754	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0006482	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0007958	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis		HP:0031035	ORPHA:210110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis	NOT	HP:0001873	ORPHA:210110	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:210110	Intermediate osteopetrosis	NOT	HP:0002901	ORPHA:210110	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000219	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000232	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000272	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000316	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000343	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000347	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000369	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000445	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000664	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000924	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0001007	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0001252	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0001256	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0001263	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0001999	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0003022	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0004325	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0005469	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0008551	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0009928	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0030084	ORPHA:357175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000337	ORPHA:357175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0000494	ORPHA:357175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0002342	ORPHA:357175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357175	Short ulna-dysmorphism-hypotonia-intellectual disability syndrome		HP:0010864	ORPHA:357175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2777	Osteomesopyknosis		HP:0011001	ORPHA:2777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2777	Osteomesopyknosis		HP:0002650	ORPHA:2777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2777	Osteomesopyknosis		HP:0002808	ORPHA:2777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2777	Osteomesopyknosis		HP:0003312	ORPHA:2777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2777	Osteomesopyknosis		HP:0100861	ORPHA:2777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2777	Osteomesopyknosis		HP:0001939	ORPHA:2777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2777	Osteomesopyknosis		HP:0003103	ORPHA:2777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001249	ORPHA:1445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001250	ORPHA:1445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001263	ORPHA:1445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001999	ORPHA:1445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000141	ORPHA:1445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000252	ORPHA:1445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000789	ORPHA:1445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0002353	ORPHA:1445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000027	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000750	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000765	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000873	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0000992	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001159	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001257	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001288	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001360	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0001627	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0002123	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0002650	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0004283	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0004313	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0004322	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0007565	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0008467	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0011171	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0025190	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0030039	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0030084	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1445	Ring chromosome 21 syndrome		HP:0200055	ORPHA:1445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0002353	ORPHA:1444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0032671	ORPHA:1444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0000708	ORPHA:1444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0001268	ORPHA:1444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0011153	ORPHA:1444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0031951	ORPHA:1444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0200134	ORPHA:1444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0000736	ORPHA:1444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0001249	ORPHA:1444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0001328	ORPHA:1444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0001510	ORPHA:1444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1444	Ring chromosome 20 syndrome		HP:0012758	ORPHA:1444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2779	Osteopathia striata-pigmentary dermopathy-white forelock syndrome		HP:0000940	ORPHA:2779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2779	Osteopathia striata-pigmentary dermopathy-white forelock syndrome		HP:0000944	ORPHA:2779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2779	Osteopathia striata-pigmentary dermopathy-white forelock syndrome		HP:0002211	ORPHA:2779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2779	Osteopathia striata-pigmentary dermopathy-white forelock syndrome		HP:0002644	ORPHA:2779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2779	Osteopathia striata-pigmentary dermopathy-white forelock syndrome		HP:0007412	ORPHA:2779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2779	Osteopathia striata-pigmentary dermopathy-white forelock syndrome		HP:0010740	ORPHA:2779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2779	Osteopathia striata-pigmentary dermopathy-white forelock syndrome		HP:0100670	ORPHA:2779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000252	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000316	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000347	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000358	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000365	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000369	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000426	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000729	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0000973	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0001249	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0001263	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0001510	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0001762	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0002002	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0002194	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1443	Ring chromosome 19 syndrome		HP:0011220	ORPHA:1443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0000252	ORPHA:1442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0001249	ORPHA:1442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0001263	ORPHA:1442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0004322	ORPHA:1442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0100543	ORPHA:1442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0000812	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0000821	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0001250	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0001252	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0001511	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0001762	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0002463	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0012448	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1442	Ring chromosome 18 syndrome		HP:0410030	ORPHA:1442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0000957	ORPHA:1441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001249	ORPHA:1441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001250	ORPHA:1441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001263	ORPHA:1441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0004322	ORPHA:1441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0012045	ORPHA:1441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0000252	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0000286	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0000347	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0000431	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0000750	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001252	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001328	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001339	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001510	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001511	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0001770	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1441	Ring chromosome 17 syndrome		HP:0030084	ORPHA:1441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0001249	ORPHA:1440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0001250	ORPHA:1440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000708	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000750	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0001252	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0001270	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0001511	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0002719	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0005484	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0008897	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0025373	ORPHA:1440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000486	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000501	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000518	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000545	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000612	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000752	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0000957	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0001273	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0002650	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1440	Ring chromosome 14 syndrome		HP:0007703	ORPHA:1440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000294	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000455	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000463	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000506	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000629	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000817	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0001249	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0002079	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0002465	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0010818	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0010841	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0012105	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0012110	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0100704	ORPHA:411986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000232	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000322	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000341	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000414	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000426	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000527	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000528	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000574	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000664	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0000733	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0001252	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0001336	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0002121	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0002384	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0002521	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0002540	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0009748	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0009904	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0010819	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0012469	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0012471	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411986	Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome		HP:0040159	ORPHA:411986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0000238	ORPHA:2770	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0000657	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0000708	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0000727	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0000734	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0000737	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0000751	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0001250	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0001257	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0001376	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002072	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002119	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002120	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002167	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002354	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002376	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002488	ORPHA:2770	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002514	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002652	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002653	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0002829	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0004349	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0005930	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0009124	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0010524	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0012062	ORPHA:2770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0012719	ORPHA:2770	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2770	Nasu-Hakola disease		HP:0100022	ORPHA:2770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0000325	ORPHA:2771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0000926	ORPHA:2771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0000939	ORPHA:2771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0001059	ORPHA:2771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0001387	ORPHA:2771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0001762	ORPHA:2771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0002093	ORPHA:2771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0002645	ORPHA:2771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0002650	ORPHA:2771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0002757	ORPHA:2771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0002804	ORPHA:2771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0002808	ORPHA:2771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0004322	ORPHA:2771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2771	Bruck syndrome		HP:0006487	ORPHA:2771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000028	ORPHA:2772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000062	ORPHA:2772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000252	ORPHA:2772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000316	ORPHA:2772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000358	ORPHA:2772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000518	ORPHA:2772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000592	ORPHA:2772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0000772	ORPHA:2772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0001195	ORPHA:2772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0001511	ORPHA:2772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0001629	ORPHA:2772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0002119	ORPHA:2772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0002269	ORPHA:2772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0002757	ORPHA:2772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0002983	ORPHA:2772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0004383	ORPHA:2772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0005474	ORPHA:2772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0001382	ORPHA:2772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0007360	ORPHA:2772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0008736	ORPHA:2772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2772	Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome		HP:0008873	ORPHA:2772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0000478	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0000504	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0000648	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0001249	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0001250	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0002645	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0002757	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2773	Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome		HP:0011344	ORPHA:2773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000047	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000135	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000160	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000233	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000248	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000252	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000271	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000272	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000286	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000294	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000322	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000385	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000426	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000431	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000494	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000601	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000932	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001270	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001488	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0002120	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0002553	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0004322	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0004425	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0007687	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0008846	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0009088	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0009899	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0011344	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0012368	ORPHA:1449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001000	ORPHA:1449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001238	ORPHA:1449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0002119	ORPHA:1449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0003196	ORPHA:1449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0009933	ORPHA:1449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0030148	ORPHA:1449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000034	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000175	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000303	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000329	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000463	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000486	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000565	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000954	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000957	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001317	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0002857	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0002861	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0004619	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0007481	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0200055	ORPHA:1449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0000193	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001357	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001360	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0001696	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0004209	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0009099	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0009237	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1449	Ring chromosome 7 syndrome		HP:0009779	ORPHA:1449	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0000252	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0000286	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0000316	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0000400	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0000431	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0000470	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0002093	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0002162	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0004322	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0009882	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1448	Ring chromosome 6 syndrome		HP:0100589	ORPHA:1448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0000093	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0000112	ORPHA:2774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0000325	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0000347	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0000431	ORPHA:2774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0000506	ORPHA:2774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0000520	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0001225	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0001288	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0001376	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0001495	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0001504	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0001561	ORPHA:2774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0002714	ORPHA:2774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0002797	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0003019	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0003100	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0003457	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0004326	ORPHA:2774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0005930	ORPHA:2774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2774	Multicentric carpo-tarsal osteolysis with or without nephropathy		HP:0100490	ORPHA:2774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1447	Ring chromosome 4 syndrome		HP:0001171	ORPHA:1447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1447	Ring chromosome 4 syndrome		HP:0006501	ORPHA:1447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1447	Ring chromosome 4 syndrome		HP:0002817	ORPHA:1447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1447	Ring chromosome 4 syndrome		HP:0040071	ORPHA:1447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0000164	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0000327	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0000455	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0000520	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0001256	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0002797	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0004322	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0009882	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2776	Autosomal recessive distal osteolysis syndrome		HP:0011800	ORPHA:2776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000027	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000252	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000268	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000276	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000286	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000293	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000307	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000400	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000414	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000574	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000719	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000729	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000750	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0000969	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001004	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001067	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001176	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001250	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001263	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001290	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001510	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0002066	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0002376	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0004691	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0007328	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0010808	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0011800	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0012471	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0012810	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0100797	ORPHA:1446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001274	ORPHA:1446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0001331	ORPHA:1446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1446	Ring chromosome 22 syndrome		HP:0002202	ORPHA:1446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0000028	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0000077	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0000256	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0000316	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0000356	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0000750	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0000924	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0001263	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0001270	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0001627	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314034	7p22.1 microduplication syndrome		HP:0001999	ORPHA:314034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000219	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000028	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000252	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000303	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0001250	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0001252	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0001999	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0002020	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0002719	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0008850	ORPHA:435938	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000047	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000407	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000411	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000678	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0000954	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0001182	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0001601	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0004415	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0006101	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0006380	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0006466	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0009796	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0012033	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0012385	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435938	X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome		HP:0100716	ORPHA:435938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0000819	ORPHA:46487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0000953	ORPHA:46487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0000987	ORPHA:46487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0000989	ORPHA:46487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0001056	ORPHA:46487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0001595	ORPHA:46487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0002027	ORPHA:46487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0002037	ORPHA:46487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0008066	ORPHA:46487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46487	Epidermolysis bullosa acquisita		HP:0008404	ORPHA:46487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0001249	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0001410	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0001999	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0002079	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0002361	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0002506	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0002510	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0003256	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0005484	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0010818	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0010837	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0011967	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435934	COG2-CDG		HP:0012506	ORPHA:435934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0002960	ORPHA:46488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0008066	ORPHA:46488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0200034	ORPHA:46488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0000155	ORPHA:46488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:4000027	ORPHA:46488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:4000028	ORPHA:46488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0000421	ORPHA:46488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0000989	ORPHA:46488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0002037	ORPHA:46488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0009725	ORPHA:46488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46488	Linear IgA dermatosis		HP:0009726	ORPHA:46488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46486	Mucous membrane pemphigoid		HP:0000230	ORPHA:46486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46486	Mucous membrane pemphigoid		HP:0000618	ORPHA:46486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46486	Mucous membrane pemphigoid		HP:0000987	ORPHA:46486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46486	Mucous membrane pemphigoid		HP:0002960	ORPHA:46486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46486	Mucous membrane pemphigoid		HP:0007957	ORPHA:46486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46486	Mucous membrane pemphigoid		HP:0008066	ORPHA:46486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46486	Mucous membrane pemphigoid		HP:0200097	ORPHA:46486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0000505	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0000968	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0001231	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0002213	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0007703	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0008070	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0008388	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0100804	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0200102	ORPHA:1433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0002558	ORPHA:1433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0006101	ORPHA:1433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0007791	ORPHA:1433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0008402	ORPHA:1433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0010793	ORPHA:1433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0040262	ORPHA:1433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1433	Choroidal atrophy-alopecia syndrome		HP:0045074	ORPHA:1433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2768	Blount disease		HP:0002982	ORPHA:2768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2768	Blount disease		HP:0002815	ORPHA:2768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2768	Blount disease		HP:0006491	ORPHA:2768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2768	Blount disease		HP:0010591	ORPHA:2768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2768	Blount disease		HP:0040188	ORPHA:2768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000272	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000303	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000307	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000309	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000363	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000414	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000448	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000457	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000574	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000692	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000822	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0002149	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0002650	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0002659	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0002757	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0002808	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0003103	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0003189	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0005613	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0006352	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0006660	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0009748	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0010443	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0010668	ORPHA:2769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000670	ORPHA:2769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000772	ORPHA:2769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0000921	ORPHA:2769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0003312	ORPHA:2769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0004209	ORPHA:2769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0001250	ORPHA:2769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2769	Familial osteodysplasia, Anderson type		HP:0003042	ORPHA:2769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0008163	ORPHA:95409	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0008207	ORPHA:95409	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0000953	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001324	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001508	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001824	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002014	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002017	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002019	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002027	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002039	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002615	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002960	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0003154	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0011106	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0012378	ORPHA:95409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0000083	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0000127	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0000848	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001250	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001252	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001278	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001897	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001943	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002149	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002153	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002902	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0004319	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0005976	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0008226	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0011948	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0012364	ORPHA:95409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0000823	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0000835	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0000958	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001045	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001297	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0001658	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002215	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002321	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0002829	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0003072	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0030018	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95409	Acute adrenal insufficiency		HP:0030083	ORPHA:95409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2760	OSLAM syndrome		HP:0000670	ORPHA:2760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2760	OSLAM syndrome		HP:0001874	ORPHA:2760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2760	OSLAM syndrome		HP:0002669	ORPHA:2760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2760	OSLAM syndrome		HP:0002974	ORPHA:2760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2760	OSLAM syndrome		HP:0004209	ORPHA:2760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2760	OSLAM syndrome		HP:0004322	ORPHA:2760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2760	OSLAM syndrome		HP:0005518	ORPHA:2760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001263	ORPHA:1439	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001510	ORPHA:1439	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001999	ORPHA:1439	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000252	ORPHA:1439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0007477	ORPHA:1439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0030084	ORPHA:1439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000028	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000131	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000369	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000465	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000565	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000767	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000807	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0000821	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001007	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001028	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001061	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001159	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001518	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001684	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0001810	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0002705	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0002938	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0003187	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0004207	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0008551	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1439	Ring chromosome 12 syndrome		HP:0009656	ORPHA:1439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000233	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000316	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000343	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000347	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000369	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000431	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000470	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000494	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000568	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0000767	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0001182	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0001249	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0001250	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0001252	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0001511	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0001852	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0002007	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0002251	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0002901	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0004326	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0006610	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0008678	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0009738	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1438	Ring chromosome 10 syndrome		HP:0009748	ORPHA:1438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0000828	ORPHA:2762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0001034	ORPHA:2762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0001156	ORPHA:2762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0001376	ORPHA:2762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0001482	ORPHA:2762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0002653	ORPHA:2762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0002758	ORPHA:2762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0010766	ORPHA:2762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0011987	ORPHA:2762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0012733	ORPHA:2762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0100242	ORPHA:2762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2762	Progressive osseous heteroplasia		HP:0200034	ORPHA:2762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000252	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000311	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000343	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000431	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000463	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000494	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000506	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0000508	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0002714	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0004209	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0008872	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0010720	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1437	Ring chromosome 1 syndrome		HP:0100543	ORPHA:1437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399805	Male infertility with azoospermia or oligozoospermia due to single gene mutation		HP:0000027	ORPHA:399805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399805	Male infertility with azoospermia or oligozoospermia due to single gene mutation		HP:0000118	ORPHA:399805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399805	Male infertility with azoospermia or oligozoospermia due to single gene mutation		HP:0000837	ORPHA:399805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399805	Male infertility with azoospermia or oligozoospermia due to single gene mutation		HP:0008669	ORPHA:399805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399805	Male infertility with azoospermia or oligozoospermia due to single gene mutation		HP:0008734	ORPHA:399805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399805	Male infertility with azoospermia or oligozoospermia due to single gene mutation		HP:0011961	ORPHA:399805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399805	Male infertility with azoospermia or oligozoospermia due to single gene mutation		HP:0011962	ORPHA:399805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0001156	ORPHA:1436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0002023	ORPHA:1436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0002650	ORPHA:1436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0002949	ORPHA:1436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0004322	ORPHA:1436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0005107	ORPHA:1436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0005819	ORPHA:1436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0005978	ORPHA:1436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1436	X-linked skeletal dysplasia-intellectual disability syndrome		HP:0008467	ORPHA:1436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0001376	ORPHA:2764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0001386	ORPHA:2764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0001387	ORPHA:2764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0002815	ORPHA:2764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0002829	ORPHA:2764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0000938	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0001367	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0001377	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0001382	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0003088	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0003184	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0006376	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0010885	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0011843	ORPHA:2764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0001288	ORPHA:2764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0002992	ORPHA:2764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2764	Osteochondritis dissecans		HP:0009050	ORPHA:2764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000407	ORPHA:1435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000532	ORPHA:1435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001139	ORPHA:1435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0200065	ORPHA:1435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000375	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000381	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000405	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000648	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000824	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000830	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001251	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001256	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001263	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001347	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001510	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001513	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0002066	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0002750	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0004458	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0005109	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0007663	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0007675	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0007937	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0007994	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0008245	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0008619	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0008897	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0011448	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0030532	ORPHA:1435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000486	ORPHA:1435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000639	ORPHA:1435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0000822	ORPHA:1435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001250	ORPHA:1435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0001920	ORPHA:1435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0002075	ORPHA:1435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome		HP:0003484	ORPHA:1435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome	NOT	HP:0000863	ORPHA:1435	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome	NOT	HP:0010625	ORPHA:1435	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1435	Xq21 microdeletion syndrome	NOT	HP:0011748	ORPHA:1435	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0001409	ORPHA:210136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0001433	ORPHA:210136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0002206	ORPHA:210136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0005528	ORPHA:210136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0011954	ORPHA:210136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0001873	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0002091	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0002094	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0002910	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0003281	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0006707	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0012735	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0030830	ORPHA:210136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0001685	ORPHA:210136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0002103	ORPHA:210136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210136	Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome		HP:0030829	ORPHA:210136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0000737	ORPHA:30925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0000873	ORPHA:30925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0001254	ORPHA:30925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0001510	ORPHA:30925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0001824	ORPHA:30925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0001945	ORPHA:30925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0001959	ORPHA:30925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0002013	ORPHA:30925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30925	Hereditary arginine vasopressin deficiency		HP:0002014	ORPHA:30925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0000774	ORPHA:1423	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0003026	ORPHA:1423	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0003950	ORPHA:1423	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0005616	ORPHA:1423	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0005789	ORPHA:1423	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0009826	ORPHA:1423	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0000347	ORPHA:1423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0001561	ORPHA:1423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0000158	ORPHA:1423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0000969	ORPHA:1423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0002098	ORPHA:1423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1423	Lethal recessive chondrodysplasia		HP:0002983	ORPHA:1423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000252	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000400	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000506	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000774	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0001249	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0001511	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0002644	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0002983	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0003043	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0003510	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0004330	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0005622	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0009803	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0010049	ORPHA:1422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000037	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000486	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000490	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000567	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000581	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0000616	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0006872	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1422	Chondrodysplasia-difference of sex development syndrome		HP:0007676	ORPHA:1422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000478	ORPHA:220386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000601	ORPHA:220386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001508	ORPHA:220386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001510	ORPHA:220386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002033	ORPHA:220386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0004322	ORPHA:220386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0011968	ORPHA:220386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000161	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000175	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000193	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000218	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000252	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000407	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000457	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000708	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000716	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000737	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000739	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000741	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001249	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001250	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001254	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001257	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001328	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001344	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002013	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002015	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002019	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002020	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002270	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002363	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002451	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002540	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002793	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002871	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0005968	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0006528	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0006979	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0007018	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0007301	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0008947	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0010654	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0011442	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0011951	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0012285	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0040327	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0045005	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0100704	ORPHA:220386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000119	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000238	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000256	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000818	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000824	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000871	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000873	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0000924	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001274	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001371	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0001627	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002465	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002650	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0002827	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0006315	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0008936	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0009914	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0009932	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0011471	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0011787	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0012718	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0012806	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0031860	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220386	Semilobar holoprosencephaly		HP:0040064	ORPHA:220386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000153	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000159	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000288	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000358	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000369	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000600	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000772	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000921	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0002094	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0002098	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0002205	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0002878	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0002937	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0003312	ORPHA:2759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000286	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000396	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000431	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000453	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0000494	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0001166	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0001561	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0001622	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0004209	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0001382	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0009896	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0010295	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2759	Imperforate oropharynx-costovertebral anomalies syndrome		HP:0011302	ORPHA:2759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0003095	ORPHA:36237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0005406	ORPHA:36237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0008066	ORPHA:36237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0010783	ORPHA:36237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0100763	ORPHA:36237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0100806	ORPHA:36237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0100820	ORPHA:36237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36237	Bullous impetigo		HP:0200039	ORPHA:36237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0012418	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0031246	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0031864	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0032177	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0032308	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0100749	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0001254	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0001289	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0001882	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002105	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002107	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002113	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002721	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0025144	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0025419	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0025439	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0031273	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0032016	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0100758	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0100806	ORPHA:36238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0000819	ORPHA:36238	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0030955	ORPHA:36238	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0001945	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0001974	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002090	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002094	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002098	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002789	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0003565	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0012735	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0032169	ORPHA:36238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002202	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002615	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0002878	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0011227	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0011897	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0011919	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36238	Staphylococcal necrotizing pneumonia		HP:0011949	ORPHA:36238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1429	Benign hereditary chorea		HP:0001288	ORPHA:1429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1429	Benign hereditary chorea		HP:0100022	ORPHA:1429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000161	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000180	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000187	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000191	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000218	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000271	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000316	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000431	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0002007	ORPHA:2750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000164	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000175	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000199	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000324	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000430	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000494	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000668	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000929	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001161	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001249	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001250	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001251	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001829	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001831	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0004097	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0004209	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0004349	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0006101	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0010579	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0011802	ORPHA:2750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000003	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000083	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000093	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000126	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000286	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000347	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000365	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000389	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000453	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000506	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000682	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000822	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000924	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0000958	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001056	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001156	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001162	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001177	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001274	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001305	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001332	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001337	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001596	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001732	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001737	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0001738	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0002208	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0002299	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0002617	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0002910	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0008070	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0008368	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0010669	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0010807	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0100267	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2750	Orofaciodigital syndrome type 1		HP:0100612	ORPHA:2750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000175	ORPHA:2751	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000161	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000190	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000199	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000218	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000431	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000685	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0001841	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0004322	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0006042	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0006101	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0006289	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0010055	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0010068	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0010100	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0010297	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0011802	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0011819	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0040019	ORPHA:2751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000220	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000347	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000405	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000411	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000506	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000679	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0001161	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0001162	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0001263	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0002104	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0002789	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0004987	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0005349	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0005736	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0005873	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0006342	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0006695	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0007768	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0008947	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0009826	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0010230	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0011087	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0030680	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0100702	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0100874	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0410033	ORPHA:2751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000050	ORPHA:2751	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0000695	ORPHA:2751	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0002069	ORPHA:2751	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2751	Orofaciodigital syndrome type 2		HP:0009776	ORPHA:2751	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000407	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000463	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0001367	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0003468	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0003498	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0005280	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0011800	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0040163	ORPHA:1427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000175	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000193	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000347	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0001156	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0002656	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0006375	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0009826	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0011314	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0011867	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0012368	ORPHA:1427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000162	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000358	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000470	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000520	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000926	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0001376	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0001561	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0001852	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0002758	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0002834	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0002938	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0002982	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0003037	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0003417	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0009803	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0010049	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0010502	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0100569	ORPHA:1427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000486	ORPHA:1427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0000540	ORPHA:1427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia		HP:0025573	ORPHA:1427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia	NOT	HP:0000518	ORPHA:1427	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia	NOT	HP:0000541	ORPHA:1427	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia	NOT	HP:0007964	ORPHA:1427	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1427	Autosomal recessive otospondylomegaepiphyseal dysplasia	NOT	HP:0011003	ORPHA:1427	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0000347	ORPHA:1426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0000774	ORPHA:1426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0000926	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0001004	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0001156	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0001362	ORPHA:1426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0001881	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0002983	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0003312	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0004331	ORPHA:1426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0006619	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0008890	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0008905	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0009106	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0011800	ORPHA:1426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0011849	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0100569	ORPHA:1426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1426	Greenberg dysplasia		HP:0100602	ORPHA:1426	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002615	ORPHA:36234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0031273	ORPHA:36234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0032169	ORPHA:36234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001289	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001581	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001649	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001942	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001945	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002027	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002098	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002151	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0003326	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0011799	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0012531	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0100537	ORPHA:36234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0000083	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0000099	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0000246	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0000988	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001287	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001369	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0001873	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002013	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002014	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002018	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002090	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002383	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002586	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002754	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002789	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002814	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002817	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0002901	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0003073	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0003095	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0003236	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0003259	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0005521	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0008066	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0011355	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0011947	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0012115	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0012819	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0025143	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0025439	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0025615	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0030005	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0031364	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0031691	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0031864	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0032170	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0032237	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0032238	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0032675	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0040189	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0100614	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0100658	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0100806	ORPHA:36234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0000010	ORPHA:36234	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36234	Bacterial toxic-shock syndrome		HP:0000969	ORPHA:36234	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000463	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000470	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000501	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000520	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000944	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0001249	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0001591	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0002999	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0003366	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0003510	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0005280	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0005616	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0001382	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0008873	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0010318	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0100490	ORPHA:1425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000358	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000499	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0000592	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0001629	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0002650	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0002673	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0002812	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0002816	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0002974	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0003042	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0004209	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0008070	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1425	Desbuquois syndrome		HP:0200055	ORPHA:1425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000157	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000161	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000168	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000190	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000202	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000252	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000278	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000316	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000347	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000356	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000358	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000369	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000405	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000445	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000453	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000457	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000496	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001162	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001177	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001249	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001263	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001328	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001367	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001373	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001511	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001562	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001601	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0002205	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0002970	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0002983	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0003196	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0003510	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0005772	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0006101	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0008734	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0009118	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0010285	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0010469	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0010566	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0011267	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0011830	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0030868	ORPHA:2753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000175	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000176	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000193	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000520	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001171	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001508	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001510	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0002120	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0002705	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0011968	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0012157	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0100308	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0100490	ORPHA:2753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000104	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000143	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000322	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0000598	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0001800	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0002023	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0002089	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0004871	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0005944	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0008207	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0008678	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0011255	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0025023	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2753	Orofaciodigital syndrome type 4		HP:0030680	ORPHA:2753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000175	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000180	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000190	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000199	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000218	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000276	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000286	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000316	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000347	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000358	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000405	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000455	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000565	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000639	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001156	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001159	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001249	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001251	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001252	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001263	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001288	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001290	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001508	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001510	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0002007	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0002419	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0004322	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0004422	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0007036	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0008689	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0008872	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0011802	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0040019	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0100258	ORPHA:2754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000104	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0000426	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001161	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001250	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001320	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001337	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001627	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0001829	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0002104	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0002269	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0002444	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0002553	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0002876	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0006145	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0007370	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0008678	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0009084	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2754	Orofaciodigital syndrome type 6		HP:0100260	ORPHA:2754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0000126	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001195	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001629	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001631	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001636	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001643	ORPHA:210122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001647	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001650	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001734	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0001746	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0002023	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0002092	ORPHA:210122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0002098	ORPHA:210122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0002251	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0002566	ORPHA:210122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0002575	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0002580	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0003468	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0004383	ORPHA:210122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0006695	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0010882	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0011467	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210122	Congenital alveolar capillary dysplasia		HP:0100867	ORPHA:210122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0000444	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0000670	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0000962	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0001034	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0001595	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0001798	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0002293	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0004404	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0007471	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0007502	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0030503	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0040211	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69125	Anonychia with flexural pigmentation		HP:0100872	ORPHA:69125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0001251	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0001260	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0002066	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0002078	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0002136	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0002345	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0002719	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0006801	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0007979	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0010904	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210128	Urocanic aciduria		HP:0012237	ORPHA:210128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0000093	ORPHA:69126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0001061	ORPHA:69126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0001369	ORPHA:69126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0001376	ORPHA:69126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0001945	ORPHA:69126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0002716	ORPHA:69126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0002829	ORPHA:69126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0010702	ORPHA:69126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0012378	ORPHA:69126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0012649	ORPHA:69126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0100280	ORPHA:69126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0100614	ORPHA:69126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0100651	ORPHA:69126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0200039	ORPHA:69126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69126	PAPA syndrome		HP:0200042	ORPHA:69126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0002650	ORPHA:2744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0002808	ORPHA:2744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0007817	ORPHA:2744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0000252	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0000470	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0000486	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0000505	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0000639	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0001252	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0002750	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0003198	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0003508	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0009921	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0100543	ORPHA:2744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0000407	ORPHA:2744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2744	Horizontal gaze palsy with progressive scoliosis		HP:0001250	ORPHA:2744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1412	Tarsal-carpal coalition syndrome		HP:0003028	ORPHA:1412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1412	Tarsal-carpal coalition syndrome		HP:0004322	ORPHA:1412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1412	Tarsal-carpal coalition syndrome		HP:0008368	ORPHA:1412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000348	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000455	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000508	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000537	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0002007	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0005280	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0005453	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0009119	ORPHA:488437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000256	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000260	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000316	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0000358	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0001511	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0001518	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0002693	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0004322	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0005494	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0010291	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia		HP:0011330	ORPHA:488437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia	NOT	HP:0000077	ORPHA:488437	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia	NOT	HP:0000820	ORPHA:488437	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:488437	SIX2-related frontonasal dysplasia	NOT	HP:0001263	ORPHA:488437	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000316	ORPHA:2745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000343	ORPHA:2745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000431	ORPHA:2745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0011220	ORPHA:2745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000047	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000175	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000349	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000463	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000506	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000508	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000736	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001249	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001273	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001328	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001999	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002119	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0004322	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0008751	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0012758	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0410030	ORPHA:2745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000023	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000028	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000048	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000049	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000076	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000079	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000119	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000126	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000218	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000239	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000252	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000347	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000358	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000365	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000369	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000494	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000729	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000776	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001274	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001305	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001363	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001537	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001539	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001627	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001629	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001631	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001643	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001655	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0001680	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002015	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002023	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002079	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002100	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002465	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002575	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002616	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0004397	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0004467	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0005301	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0005487	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0006817	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0008872	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0010307	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0012443	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0031936	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0100879	ORPHA:2745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000486	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000539	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000668	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000695	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0000813	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0002779	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0003422	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0010296	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2745	Opitz GBBB syndrome		HP:0010518	ORPHA:2745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0000239	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0000256	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0000592	ORPHA:2746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0000767	ORPHA:2746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0000774	ORPHA:2746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0000944	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0001156	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0001182	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0001252	ORPHA:2746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0001387	ORPHA:2746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0001744	ORPHA:2746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0002007	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0002093	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0002205	ORPHA:2746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0002240	ORPHA:2746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0002750	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0003173	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0003175	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0003177	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0003196	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0003510	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0005280	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0005469	ORPHA:2746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0005930	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0008479	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0011304	ORPHA:2746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2746	Opsismodysplasia		HP:0100569	ORPHA:2746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1410	Uncombable hair syndrome		HP:0001595	ORPHA:1410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1410	Uncombable hair syndrome		HP:0002208	ORPHA:1410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1410	Uncombable hair syndrome		HP:0002224	ORPHA:1410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1410	Uncombable hair syndrome		HP:0002552	ORPHA:1410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1410	Uncombable hair syndrome		HP:0011364	ORPHA:1410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1410	Uncombable hair syndrome		HP:0002232	ORPHA:1410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000278	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000324	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000377	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000437	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000455	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000465	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000470	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000506	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000574	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000772	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000929	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000935	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000938	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0001054	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0001256	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0001773	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0002750	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0003298	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0006402	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0006429	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0010761	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0012036	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0012368	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0012810	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0200055	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0430007	ORPHA:488434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488434	Camptodactyly syndrome, Guadalajara type 3		HP:0000054	ORPHA:488434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0000083	ORPHA:220393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0000217	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0000670	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0000951	ORPHA:220393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0001324	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0001369	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0001371	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0001635	ORPHA:220393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002015	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002017	ORPHA:220393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002020	ORPHA:220393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002024	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002092	ORPHA:220393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002094	ORPHA:220393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002113	ORPHA:220393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002206	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002797	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002829	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0002960	ORPHA:220393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0030016	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0030142	ORPHA:220393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0100520	ORPHA:220393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0100585	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0100735	ORPHA:220393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0100958	ORPHA:220393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220393	Diffuse cutaneous systemic sclerosis		HP:0200042	ORPHA:220393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0000365	ORPHA:79394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0000491	ORPHA:79394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0000656	ORPHA:79394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0000966	ORPHA:79394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0000982	ORPHA:79394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0000989	ORPHA:79394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0001019	ORPHA:79394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0001508	ORPHA:79394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0001596	ORPHA:79394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0001597	ORPHA:79394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0004322	ORPHA:79394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0008064	ORPHA:79394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79394	Congenital ichthyosiform erythroderma		HP:0200020	ORPHA:79394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0009926	ORPHA:57145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0030953	ORPHA:57145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0032148	ORPHA:57145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0000508	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0000711	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0000713	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0000975	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0001069	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0002076	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0031284	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0031417	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0031731	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0100661	ORPHA:57145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0000282	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0000613	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0000616	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0001041	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0001742	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0002018	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0030766	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0040264	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0100540	ORPHA:57145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57145	SUNCT syndrome		HP:0002013	ORPHA:57145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0000972	ORPHA:79395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0007503	ORPHA:79395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0010491	ORPHA:79395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0000962	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0000982	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0001036	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0007465	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0007479	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0025114	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0025525	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0032541	ORPHA:79395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0001596	ORPHA:79395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0001805	ORPHA:79395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0008404	ORPHA:79395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0025092	ORPHA:79395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0040162	ORPHA:79395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis		HP:0000707	ORPHA:79395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79395	Keratoderma hereditarium mutilans with ichthyosis	NOT	HP:0000407	ORPHA:79395	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0000982	ORPHA:79396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001030	ORPHA:79396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0008066	ORPHA:79396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0008404	ORPHA:79396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0010783	ORPHA:79396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0011354	ORPHA:79396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0000953	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001056	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001057	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001075	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001510	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001581	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001596	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001903	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0006297	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0007589	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0007599	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0011471	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0011968	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0100699	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0200097	ORPHA:79396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0000540	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0000613	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001010	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001263	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001363	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001508	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001600	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001601	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001609	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0001805	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0002119	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0002719	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0002780	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0003073	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0004313	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0005483	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0006934	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0007483	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0007957	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0008944	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0010298	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0100806	ORPHA:79396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79396	Autosomal dominant generalized epidermolysis bullosa simplex, severe form		HP:0006739	ORPHA:79396	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0001070	ORPHA:79397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0003341	ORPHA:79397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0007427	ORPHA:79397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0007585	ORPHA:79397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0008066	ORPHA:79397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0009123	ORPHA:79397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0001034	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0002164	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0005590	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0007556	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0008404	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0009719	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0010765	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0045059	ORPHA:79397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0000164	ORPHA:79397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0000992	ORPHA:79397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0001056	ORPHA:79397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0001596	ORPHA:79397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79397	Epidermolysis bullosa simplex with mottled pigmentation		HP:0200097	ORPHA:79397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0001369	ORPHA:1416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0001386	ORPHA:1416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0002829	ORPHA:1416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0005108	ORPHA:1416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0100593	ORPHA:1416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0002758	ORPHA:1416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0000934	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0001373	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0001376	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0001387	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0001945	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0004349	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0012649	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0031013	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0045082	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0100769	ORPHA:1416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1416	Familial calcium pyrophosphate deposition		HP:0001250	ORPHA:1416	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001336	ORPHA:324290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0100318	ORPHA:324290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0000708	ORPHA:324290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001260	ORPHA:324290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001347	ORPHA:324290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001250	ORPHA:324290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001251	ORPHA:324290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001268	ORPHA:324290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001285	ORPHA:324290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0001289	ORPHA:324290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0002300	ORPHA:324290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324290	PRDM8-related progressive myoclonus epilepsy		HP:0011999	ORPHA:324290	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0000962	ORPHA:79399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0003341	ORPHA:79399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0007585	ORPHA:79399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0008066	ORPHA:79399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0005585	ORPHA:79399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0005590	ORPHA:79399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0007556	ORPHA:79399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0010765	ORPHA:79399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0000164	ORPHA:79399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0001034	ORPHA:79399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0001056	ORPHA:79399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0008404	ORPHA:79399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0009123	ORPHA:79399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0009719	ORPHA:79399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0200097	ORPHA:79399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0000989	ORPHA:79399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79399	Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form		HP:0200034	ORPHA:79399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0000485	ORPHA:2741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0000501	ORPHA:2741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0000618	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0001376	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0002974	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0002983	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0003027	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0003042	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0004348	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0005048	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0005446	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0006055	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0006439	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0006441	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0006501	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0007957	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0009773	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0012478	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2741	Ophthalmomandibulomelic dysplasia		HP:0100490	ORPHA:2741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000202	ORPHA:1415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000384	ORPHA:1415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0004467	ORPHA:1415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000377	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000580	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0001638	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0001680	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0002566	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0004297	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0004322	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0012437	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0100890	ORPHA:1415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000076	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000126	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000148	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0000776	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0001629	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0001631	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0001643	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0002019	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0002023	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0002245	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:0004942	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1415	Hardikar syndrome		HP:6000413	ORPHA:1415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001324	ORPHA:37553	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0003768	ORPHA:37553	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0003752	ORPHA:37553	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000164	ORPHA:37553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000347	ORPHA:37553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001657	ORPHA:37553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001999	ORPHA:37553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0004308	ORPHA:37553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0004322	ORPHA:37553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0008153	ORPHA:37553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000218	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000219	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000316	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000324	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000325	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000327	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000337	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000369	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000414	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000431	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000677	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000678	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000859	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001250	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001328	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001382	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001510	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001644	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001664	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001773	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001864	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001962	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0002650	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0004691	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0005135	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0005147	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0005184	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0006335	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0006682	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0006696	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0007215	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0011073	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0012745	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0012758	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0025072	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0030799	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0031677	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0200055	ORPHA:37553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000089	ORPHA:37553	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0000124	ORPHA:37553	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37553	Andersen-Tawil syndrome		HP:0001279	ORPHA:37553	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0000952	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0001000	ORPHA:1414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0001004	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0001012	ORPHA:1414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0001080	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0001394	ORPHA:1414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0001409	ORPHA:1414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0001744	ORPHA:1414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0002017	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0002027	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0002239	ORPHA:1414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0002240	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0002653	ORPHA:1414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0003077	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0003110	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0004349	ORPHA:1414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0006566	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0011985	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0012378	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1414	Cholestasis-lymphedema syndrome		HP:0100763	ORPHA:1414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0000818	ORPHA:276152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0000843	ORPHA:276152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0002897	ORPHA:276152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0003072	ORPHA:276152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0003165	ORPHA:276152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0008208	ORPHA:276152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0000825	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0000845	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0000854	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0001031	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0002014	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0002044	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0002574	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0002893	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0004398	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0006767	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0006772	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0008256	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0008283	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0010615	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0011760	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0011761	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0012091	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0012197	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0030445	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0100633	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0100634	ORPHA:276152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0003118	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0006780	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0007449	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0008291	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0010783	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0010788	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0012030	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0012334	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0030079	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0030688	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0100570	ORPHA:276152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276152	Multiple endocrine neoplasia type 4		HP:0100522	ORPHA:276152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0000221	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0000508	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0000597	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0000602	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0001249	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0001263	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0001328	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0007703	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0012246	ORPHA:2743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0000545	ORPHA:2743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0010628	ORPHA:2743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0000512	ORPHA:2743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2743	Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome		HP:0002301	ORPHA:2743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0000246	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0000403	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0001508	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0001888	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0002014	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0002788	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0002849	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0002960	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0003212	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0005354	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0005368	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0005390	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0005403	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0006532	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0010444	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0010976	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0011123	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0012393	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0025379	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:277	Severe combined immunodeficiency due to adenosine deaminase deficiency		HP:0030813	ORPHA:277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000924	ORPHA:508533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001263	ORPHA:508533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001270	ORPHA:508533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0004565	ORPHA:508533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000252	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000765	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001156	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001230	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001249	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001252	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001265	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001328	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001888	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001999	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002007	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002808	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002813	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002867	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003196	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003311	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003319	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003375	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003498	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0004313	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0005403	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0008807	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0009768	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0009803	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0010049	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0025336	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0031381	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0032061	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0045060	ORPHA:508533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000085	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000160	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000194	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000212	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000276	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000280	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000293	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000343	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000347	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000414	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000463	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000490	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000520	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000639	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000733	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0000960	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001177	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001250	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001276	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001290	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001344	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001347	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001363	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001561	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001634	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0001830	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002079	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002119	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002179	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002197	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002240	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002307	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002341	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002540	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002676	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002750	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002850	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002938	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002987	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0002996	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003051	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003189	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0003212	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0004315	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0004430	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0004894	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0005280	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0005306	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0032218	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0005415	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0005619	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0006532	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0008445	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0008462	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0008763	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0008936	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0009053	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0008936	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0009826	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0011166	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0011344	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0030320	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508533	Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome		HP:0100865	ORPHA:508533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0001888	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0001954	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002090	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0032218	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0010701	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0031381	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0031397	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0040218	ORPHA:276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0000988	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002014	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002718	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002720	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0004315	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0005390	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0012735	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0031545	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0045080	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0100806	ORPHA:276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0001508	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002728	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002732	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0005353	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0005376	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0005406	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0005428	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0009098	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0011370	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0030813	ORPHA:276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0000952	ORPHA:276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002240	ORPHA:276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0002665	ORPHA:276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0003237	ORPHA:276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276	T-B+ severe combined immunodeficiency due to gamma chain deficiency		HP:0005523	ORPHA:276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0003125	ORPHA:99147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0004377	ORPHA:99147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0008151	ORPHA:99147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0008330	ORPHA:99147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0030129	ORPHA:99147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0030680	ORPHA:99147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0000132	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0000421	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0000471	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0000790	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0000978	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001642	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001650	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001653	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001659	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001897	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001931	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001933	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0001934	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0002239	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0002249	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0002615	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0005261	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0005505	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0025406	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0100608	ORPHA:99147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99147	Acquired von Willebrand syndrome		HP:0002170	ORPHA:99147	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003326	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0005110	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0006677	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0007010	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0009027	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0012248	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0012378	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0030192	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0030319	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0031466	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0100543	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0100786	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0410011	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000026	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000029	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000144	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000467	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000483	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000540	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000602	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000712	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001324	ORPHA:273	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001262	ORPHA:273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002460	ORPHA:273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003740	ORPHA:273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0007787	ORPHA:273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0031546	ORPHA:273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0100284	ORPHA:273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000708	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001288	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002494	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002870	ORPHA:273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000716	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000729	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000736	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000739	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000802	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000815	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000819	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000842	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000855	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000867	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001081	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001256	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001260	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001263	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001268	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001319	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001328	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001349	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001488	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001558	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001561	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001596	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001762	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002014	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002019	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002093	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002120	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002234	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002500	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002527	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002747	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002878	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002910	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002926	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003124	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003202	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003693	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003701	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003722	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0004389	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0004755	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0004887	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0006889	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0007663	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0007941	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0008872	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0009113	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0009830	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0010794	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0010804	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0010952	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0011470	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0011999	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0012899	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0012901	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0012903	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0025169	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0040171	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0040173	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0200136	ORPHA:273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000717	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000718	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0000824	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0001644	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0002540	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003003	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003477	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003547	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0003749	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0008069	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0008770	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0012054	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0012114	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0025318	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0030692	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:273	Steinert myotonic dystrophy		HP:0040198	ORPHA:273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000238	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000248	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000268	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000298	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000501	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000505	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000518	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000545	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000648	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000750	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0000767	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001250	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001252	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001263	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001288	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001357	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001371	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001511	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001612	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0001644	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0002119	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0002353	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0003198	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0003457	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0003560	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0007260	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0007370	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0007973	ORPHA:272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0010864	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0030046	ORPHA:272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:272	Congenital muscular dystrophy, Fukuyama type		HP:0100490	ORPHA:272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0002718	ORPHA:275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0002720	ORPHA:275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0004315	ORPHA:275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0005390	ORPHA:275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0200043	ORPHA:275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0200117	ORPHA:275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0000388	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0000988	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0001045	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0001508	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0002960	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0004429	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0005681	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0009098	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0011107	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0011274	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0031123	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0045080	ORPHA:275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275	Severe combined immunodeficiency due to DCLRE1C deficiency		HP:0000872	ORPHA:275	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0011871	ORPHA:274	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0001892	ORPHA:274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0001902	ORPHA:274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0011879	ORPHA:274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0040185	ORPHA:274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0000132	ORPHA:274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0000967	ORPHA:274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0002239	ORPHA:274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0004406	ORPHA:274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0006298	ORPHA:274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0007420	ORPHA:274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0000225	ORPHA:274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0000978	ORPHA:274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0002248	ORPHA:274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0004846	ORPHA:274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0012143	ORPHA:274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0012587	ORPHA:274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0001250	ORPHA:274	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0002076	ORPHA:274	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0002099	ORPHA:274	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:274	Bernard-Soulier syndrome		HP:0008738	ORPHA:274	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0010535	ORPHA:270	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0100543	ORPHA:270	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0000508	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0000602	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0002015	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0003198	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0003200	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0003302	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0003805	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0004303	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0012378	ORPHA:270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0000183	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0001618	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0003325	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0003327	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0011968	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0012473	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0012531	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0012548	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0030319	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0032342	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0034045	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0100304	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:6001011	ORPHA:270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0000298	ORPHA:270	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:270	Oculopharyngeal muscular dystrophy		HP:0003236	ORPHA:270	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0000316	ORPHA:1522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0000405	ORPHA:1522	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0000407	ORPHA:1522	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0000431	ORPHA:1522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0000505	ORPHA:1522	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0000506	ORPHA:1522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0000944	ORPHA:1522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0001291	ORPHA:1522	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0002652	ORPHA:1522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0004493	ORPHA:1522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0005280	ORPHA:1522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0010628	ORPHA:1522	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1522	Craniometaphyseal dysplasia		HP:0011002	ORPHA:1522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000316	ORPHA:1521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000445	ORPHA:1521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000455	ORPHA:1521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0001363	ORPHA:1521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0004112	ORPHA:1521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0009116	ORPHA:1521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000136	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000154	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000200	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000218	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000465	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0000486	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0001159	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0001231	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0001357	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0001464	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0001540	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0002162	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0002558	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0006008	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0006709	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0009930	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0011959	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0012243	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0030867	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1521	Craniofrontonasal dysplasia-Poland anomaly syndrome		HP:0045075	ORPHA:1521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000407	ORPHA:2855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000837	ORPHA:2855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000013	ORPHA:2855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000786	ORPHA:2855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0008209	ORPHA:2855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0010464	ORPHA:2855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000027	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000175	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000218	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000813	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000869	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0000876	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0001251	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0001263	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0001328	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0001513	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0001519	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0003477	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2855	Perrault syndrome		HP:0007256	ORPHA:2855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2856	Persistent Müllerian duct syndrome		HP:0000023	ORPHA:2856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2856	Persistent Müllerian duct syndrome		HP:0000028	ORPHA:2856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2856	Persistent Müllerian duct syndrome		HP:0000037	ORPHA:2856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000047	ORPHA:1520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000049	ORPHA:1520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000164	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000202	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000218	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000248	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000252	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000316	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000324	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000349	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000407	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000431	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000457	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000474	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000494	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000767	ORPHA:1520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000776	ORPHA:1520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000889	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0000912	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001156	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001161	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001249	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001252	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001357	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001363	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001852	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0002007	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0002079	ORPHA:1520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0002162	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0002224	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0002650	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0004122	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0004209	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0001382	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0006101	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0006585	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0006709	ORPHA:1520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0008402	ORPHA:1520	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0010059	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0010719	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0100490	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1520	Craniofrontonasal dysplasia		HP:0200021	ORPHA:1520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000160	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000275	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000316	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000327	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000407	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000457	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000494	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000564	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0000581	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0003019	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0003049	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0003196	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0005280	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0009465	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0009924	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0012368	ORPHA:1529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1529	Craniofacial-deafness-hand syndrome		HP:0100490	ORPHA:1529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0000238	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0000252	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0000358	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0000505	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0000568	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0000648	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0001263	ORPHA:1528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0001274	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0001321	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0001339	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0001363	ORPHA:1528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0002007	ORPHA:1528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0002139	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0007330	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1528	Craniotelencephalic dysplasia		HP:0100842	ORPHA:1528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1527	Craniosynostosis, Philadelphia type		HP:0000637	ORPHA:1527	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1527	Craniosynostosis, Philadelphia type		HP:0001363	ORPHA:1527	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1527	Craniosynostosis, Philadelphia type		HP:0006101	ORPHA:1527	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0000252	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0000365	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0000400	ORPHA:2850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0000613	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0000815	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001156	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001171	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001249	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001250	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001252	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001371	ORPHA:2850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001510	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0001596	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0002209	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0002231	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0002353	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0002650	ORPHA:2850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0002750	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0004322	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0005105	ORPHA:2850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0008064	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0011842	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0100840	ORPHA:2850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2850	Alopecia-intellectual disability syndrome		HP:0200012	ORPHA:2850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0009027	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0011712	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0012037	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0012532	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0030002	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0030319	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0030664	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0100595	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0000541	ORPHA:269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0000572	ORPHA:269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0001250	ORPHA:269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0002093	ORPHA:269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0005115	ORPHA:269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0007898	ORPHA:269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0000298	ORPHA:269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003202	ORPHA:269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003236	ORPHA:269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003307	ORPHA:269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003323	ORPHA:269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003691	ORPHA:269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0000407	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0000491	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0000509	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0000767	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0001288	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0001538	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0002091	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0002359	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0002650	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003325	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003376	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0003458	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0004673	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0006587	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0008046	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0008959	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:269	Facioscapulohumeral dystrophy		HP:0009023	ORPHA:269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0000239	ORPHA:1525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0000929	ORPHA:1525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0000964	ORPHA:1525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0001070	ORPHA:1525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0001369	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0001386	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0001387	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0002758	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0002815	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0002829	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0002992	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0003103	ORPHA:1525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0004097	ORPHA:1525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1525	Cranio-osteoarthropathy		HP:0100760	ORPHA:1525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0003236	ORPHA:268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0007340	ORPHA:268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0008994	ORPHA:268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0001315	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0001640	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0001667	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0001761	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0003115	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0003307	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0003551	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0003691	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0003722	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0008981	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0008997	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0009046	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0011712	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0012664	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0100748	ORPHA:268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0002015	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0002072	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0002540	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0002996	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0003306	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0005085	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0008800	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0008959	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0030051	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0045054	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268	Dysferlin-related limb-girdle muscular dystrophy R2		HP:0100515	ORPHA:268	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001903	ORPHA:508542	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0005528	ORPHA:508542	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000280	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001249	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001635	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001873	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001875	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001882	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001888	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001896	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001999	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0002788	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0002863	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0004322	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0006872	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0010976	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0012758	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0031688	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0031689	ORPHA:508542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000212	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000243	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000365	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000518	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000684	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000765	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000916	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000958	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0000964	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001156	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0001482	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0002783	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0004991	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0005180	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0005792	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0010049	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0011800	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0012490	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508542	Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome		HP:0012817	ORPHA:508542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0000657	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0000739	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0001251	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0001289	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0002442	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0010523	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0010524	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0010525	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0010526	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0100704	ORPHA:54247	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0000504	ORPHA:54247	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0000551	ORPHA:54247	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0000613	ORPHA:54247	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0010522	ORPHA:54247	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0030217	ORPHA:54247	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0002354	ORPHA:54247	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0002367	ORPHA:54247	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0002463	ORPHA:54247	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0002494	ORPHA:54247	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0011098	ORPHA:54247	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54247	Posterior cortical atrophy		HP:0030216	ORPHA:54247	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003324	ORPHA:267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0001371	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0001288	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0002987	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003089	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003236	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003306	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003307	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003560	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003691	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003701	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0005879	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0006466	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0007340	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0008946	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0008981	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0009060	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0012037	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0030051	ORPHA:267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0001239	ORPHA:267	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:267	Calpain-3-related limb-girdle muscular dystrophy R1		HP:0003551	ORPHA:267	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0000767	ORPHA:261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001315	ORPHA:261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001387	ORPHA:261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0002486	ORPHA:261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003198	ORPHA:261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003236	ORPHA:261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0006785	ORPHA:261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0000912	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001288	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001771	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0002155	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0002515	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0002987	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003141	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003306	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003418	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003458	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003691	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003805	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0004631	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0008948	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0008956	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0008994	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0008997	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0011807	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0030051	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0030117	ORPHA:261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0000508	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001252	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001513	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001644	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001678	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0002650	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0002808	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0003307	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0005115	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0008064	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0009125	ORPHA:261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001605	ORPHA:261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001639	ORPHA:261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0001645	ORPHA:261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0002747	ORPHA:261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy		HP:0005155	ORPHA:261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261	Emery-Dreifuss muscular dystrophy	NOT	HP:0001249	ORPHA:261	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1509	Coxopodopatellar syndrome		HP:0001385	ORPHA:1509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1509	Coxopodopatellar syndrome		HP:0002644	ORPHA:1509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1509	Coxopodopatellar syndrome		HP:0002815	ORPHA:1509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1509	Coxopodopatellar syndrome		HP:0005930	ORPHA:1509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1509	Coxopodopatellar syndrome		HP:0006498	ORPHA:1509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000308	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000431	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000463	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000708	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0001336	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0003763	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0004322	ORPHA:324313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0007018	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0011342	ORPHA:324313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000248	ORPHA:324313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000369	ORPHA:324313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000565	ORPHA:324313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0002378	ORPHA:324313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:3000022	ORPHA:324313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000218	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000286	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000403	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000540	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000574	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000826	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000957	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0000958	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0001387	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0001537	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0001795	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0001800	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0002553	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0002650	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0003241	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0004209	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0010489	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324313	9p13 microdeletion syndrome		HP:0011330	ORPHA:324313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000013	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000047	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000054	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000144	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000147	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000786	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000815	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000823	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000939	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0002215	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0002225	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0002231	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0002750	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0004349	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008187	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008193	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008214	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008232	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008675	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0011969	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0012112	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0030349	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0040171	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0100607	ORPHA:90796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000028	ORPHA:90796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000868	ORPHA:90796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0004322	ORPHA:90796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008726	ORPHA:90796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008734	ORPHA:90796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0012041	ORPHA:90796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000033	ORPHA:90796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000037	ORPHA:90796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0000771	ORPHA:90796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0001508	ORPHA:90796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0008730	ORPHA:90796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90796	46,XY difference of sex development due to isolated 17,20-lyase deficiency		HP:0012244	ORPHA:90796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002376	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002384	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002509	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002540	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0007772	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0008947	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0011198	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0100704	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0000396	ORPHA:488613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0000767	ORPHA:488613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002126	ORPHA:488613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0012448	ORPHA:488613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome	NOT	HP:0000252	ORPHA:488613	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0001263	ORPHA:488613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0001290	ORPHA:488613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0001249	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0001250	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0001508	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0001510	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002353	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002474	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0010841	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0011968	ORPHA:488613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0000126	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0000175	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0000218	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0000486	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0000639	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488613	Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome		HP:0002069	ORPHA:488613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2843	Pentosuria		HP:0011021	ORPHA:2843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2843	Pentosuria		HP:0031979	ORPHA:2843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2843	Pentosuria		HP:0011013	ORPHA:2843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000151	ORPHA:90797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0003251	ORPHA:90797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0010463	ORPHA:90797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0011969	ORPHA:90797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0030088	ORPHA:90797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0031102	ORPHA:90797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0040307	ORPHA:90797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000047	ORPHA:90797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000062	ORPHA:90797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000771	ORPHA:90797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0008689	ORPHA:90797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0025132	ORPHA:90797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000027	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000048	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000051	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000054	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0000786	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0001620	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0008189	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0008665	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0009888	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0025134	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0025486	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0040314	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0100728	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90797	Partial androgen insensitivity syndrome		HP:0100779	ORPHA:90797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0000522	ORPHA:289483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0001249	ORPHA:289483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0001263	ORPHA:289483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0001270	ORPHA:289483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0001344	ORPHA:289483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0012434	ORPHA:289483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0000486	ORPHA:289483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0002571	ORPHA:289483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0009916	ORPHA:289483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0000384	ORPHA:289483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0000718	ORPHA:289483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0000805	ORPHA:289483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0002002	ORPHA:289483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0002015	ORPHA:289483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome		HP:0002119	ORPHA:289483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289483	Intellectual disability-alacrima-achalasia syndrome	NOT	HP:0000834	ORPHA:289483	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0009112	ORPHA:2847	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0011635	ORPHA:2847	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0002089	ORPHA:2847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0002643	ORPHA:2847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0012418	ORPHA:2847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0000766	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0000767	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0000776	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0001627	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0001631	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0001636	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0001643	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0001647	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0001718	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0001962	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0002245	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0002566	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0012718	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0100632	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2847	Pericardial and diaphragmatic defect		HP:0100749	ORPHA:2847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0001225	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0001836	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0002812	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0002938	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0003940	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0005086	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0005195	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0008812	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0100490	ORPHA:2848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0000939	ORPHA:2848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0012062	ORPHA:2848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0100864	ORPHA:2848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0001634	ORPHA:2848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0001653	ORPHA:2848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0001701	ORPHA:2848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0002102	ORPHA:2848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0001541	ORPHA:2848	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0008610	ORPHA:2848	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome		HP:0100018	ORPHA:2848	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome	NOT	HP:0002960	ORPHA:2848	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2848	Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome	NOT	HP:0033331	ORPHA:2848	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000098	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000177	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000194	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000256	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000278	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000311	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000319	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000347	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000348	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000431	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000490	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0001249	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0001252	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0001263	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0001328	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0002240	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0003196	ORPHA:2849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000028	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000187	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000286	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000358	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000369	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000391	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000463	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000842	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0002667	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0002705	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0008736	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0012090	ORPHA:2849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000023	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000268	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0000508	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0001250	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0002133	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0005306	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0007598	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0010733	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2849	Perlman syndrome		HP:0100541	ORPHA:2849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000028	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000049	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000086	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000202	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000232	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000233	ORPHA:1519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000248	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000311	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000316	ORPHA:1519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000343	ORPHA:1519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000349	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000369	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000426	ORPHA:1519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000431	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000486	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000494	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000508	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000520	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000574	ORPHA:1519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0000767	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001156	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001537	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001539	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001629	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001631	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001636	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001643	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0001831	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0002553	ORPHA:1519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0003196	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0004209	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0004467	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0006101	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0006288	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0010458	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0010751	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0011039	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0011220	ORPHA:1519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1519	SPECC1L-related hypertelorism syndrome		HP:0011675	ORPHA:1519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0001945	ORPHA:54251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0011227	ORPHA:54251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0001824	ORPHA:54251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0001903	ORPHA:54251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0002027	ORPHA:54251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0002733	ORPHA:54251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0002910	ORPHA:54251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0011897	ORPHA:54251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0100523	ORPHA:54251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0000035	ORPHA:54251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0001732	ORPHA:54251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0002014	ORPHA:54251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0002088	ORPHA:54251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0003326	ORPHA:54251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0030049	ORPHA:54251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0100763	ORPHA:54251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54251	Aseptic abscess syndrome		HP:0000077	ORPHA:54251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000154	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000256	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000280	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000286	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000294	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000336	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000343	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000431	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000463	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000470	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000527	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000574	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000774	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000885	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000926	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000939	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0000944	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0001256	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0001537	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0001639	ORPHA:1517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0001640	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0001643	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0001654	ORPHA:1517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0001869	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0002162	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0002230	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0002652	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0002673	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0002750	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0003300	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0004634	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0005616	ORPHA:1517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0006101	ORPHA:1517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0007665	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0009882	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0010059	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0010109	ORPHA:1517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1517	Cantú syndrome		HP:0012471	ORPHA:1517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0000953	ORPHA:90790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0003154	ORPHA:90790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0008730	ORPHA:90790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0000055	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0000841	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0001945	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0002013	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0002153	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0002902	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0008163	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0008221	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0030347	ORPHA:90790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0000037	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0000053	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0000707	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0000952	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0001250	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0001298	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0001508	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0001943	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0002090	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0010885	ORPHA:90790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0003002	ORPHA:90790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0012114	ORPHA:90790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90790	Congenital lipoid adrenal hyperplasia due to STAR deficency		HP:0040187	ORPHA:90790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000163	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000194	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000238	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000256	ORPHA:1516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000268	ORPHA:1516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000286	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000316	ORPHA:1516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000322	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000324	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000347	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000369	ORPHA:1516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000402	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000430	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000431	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000470	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000486	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000494	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000639	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0000960	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0001052	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0001363	ORPHA:1516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0001537	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0001643	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0002007	ORPHA:1516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0002079	ORPHA:1516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0004209	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0004322	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0009891	ORPHA:1516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1516	Non-syndromic bilambdoid and sagittal craniosynostosis		HP:0011344	ORPHA:1516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0008258	ORPHA:90791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000033	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000047	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000061	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000127	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000771	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000848	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000953	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0001944	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0001998	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0002013	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0002153	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0002615	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0002902	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0004319	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0008163	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0008665	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0011749	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0012041	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0025380	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0030088	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0031213	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0040171	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0500022	ORPHA:90791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000027	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000028	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000037	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0000808	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0001007	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0001263	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0001508	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0008730	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0008734	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0012412	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0012768	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90791	Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency		HP:0012881	ORPHA:90791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001263	ORPHA:488618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001627	ORPHA:488618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0003508	ORPHA:488618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0025550	ORPHA:488618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000518	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000554	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000722	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000750	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001252	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001256	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001344	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001629	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001631	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0007018	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0410072	ORPHA:488618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000107	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000365	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000509	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000733	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0000869	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001051	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001643	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0001655	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0002240	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0011686	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0100651	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488618	Transketolase deficiency		HP:0100716	ORPHA:488618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000164	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000232	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000268	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000269	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000286	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000463	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000545	ORPHA:1515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000601	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000639	ORPHA:1515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000668	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000679	ORPHA:1515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000682	ORPHA:1515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000691	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000767	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000774	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000939	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000940	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0000944	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0001156	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0001231	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0001363	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0002007	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0004209	ORPHA:1515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0001382	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0006101	ORPHA:1515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0008070	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0008388	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0008499	ORPHA:1515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0008905	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1515	Cranioectodermal dysplasia		HP:0009882	ORPHA:1515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0000248	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0000347	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0000446	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0000527	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0000574	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0001249	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0002230	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0003196	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0003298	ORPHA:1514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0004322	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0006101	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0007477	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0010720	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1514	Craniodigital-intellectual disability syndrome		HP:0100874	ORPHA:1514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0000592	ORPHA:2840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0001288	ORPHA:2840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0001376	ORPHA:2840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0002827	ORPHA:2840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0003100	ORPHA:2840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0003202	ORPHA:2840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0003298	ORPHA:2840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0005280	ORPHA:2840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0008839	ORPHA:2840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2840	Pelvic dysplasia-arthrogryposis of lower limbs syndrome		HP:0010767	ORPHA:2840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001252	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001270	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001324	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001612	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001939	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002020	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002375	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002540	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002878	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0003560	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0003560	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0009025	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0030091	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0030234	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0100295	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0100614	ORPHA:258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0000158	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001249	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001250	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001371	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002181	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002446	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002783	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002835	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0003457	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0005216	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0010628	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0010754	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0012747	ORPHA:258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0000194	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0000649	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001302	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001315	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001319	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001339	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0001638	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002015	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002058	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002121	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002650	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002791	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0003307	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0004325	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0004878	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0006879	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0007141	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0007359	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0010808	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0011675	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0012664	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0100543	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0100750	ORPHA:258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002092	ORPHA:258	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:258	Laminin subunit alpha 2-related congenital muscular dystrophy		HP:0002093	ORPHA:258	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000822	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000837	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008258	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0031074	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0032330	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0032362	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0040171	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0500022	ORPHA:90793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000026	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000047	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000138	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000144	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000771	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000786	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000823	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000858	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0002750	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0002900	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0003351	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0004319	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008163	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008187	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008197	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008232	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008689	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0011749	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0011969	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0031216	ORPHA:90793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000033	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000048	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000054	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0000151	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0001508	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0002221	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0002555	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0003251	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0003394	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008207	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0008730	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0010465	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90793	Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency		HP:0040314	ORPHA:90793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0000256	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0000280	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0000402	ORPHA:1513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0000405	ORPHA:1513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0000431	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0000648	ORPHA:1513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0000772	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0001249	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0002007	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0004322	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0004493	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0005019	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1513	Craniodiaphyseal dysplasia		HP:0005280	ORPHA:1513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2841	Hailey-Hailey disease		HP:0000962	ORPHA:2841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2841	Hailey-Hailey disease		HP:0010783	ORPHA:2841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2841	Hailey-Hailey disease		HP:0100792	ORPHA:2841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2841	Hailey-Hailey disease		HP:0200041	ORPHA:2841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2841	Hailey-Hailey disease		HP:0200037	ORPHA:2841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0008163	ORPHA:90794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0030348	ORPHA:90794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0031074	ORPHA:90794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0031213	ORPHA:90794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0031216	ORPHA:90794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000127	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000140	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000144	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000811	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000841	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000876	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0001007	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0001061	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0001507	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0001508	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0001824	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0001944	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0001998	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0002013	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0002153	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0002615	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0002902	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0003113	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0003154	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0003639	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0004012	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0004319	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0004322	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0005616	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0005976	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0008207	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0008665	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0011106	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0011968	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0012411	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0012417	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0012605	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0025380	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0030088	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0031066	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0500022	ORPHA:90794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000040	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000044	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000061	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000062	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000098	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0000151	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0002292	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0005268	ORPHA:90794	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0008734	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0010465	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0012412	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0025451	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0025486	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0031273	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90794	Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency		HP:0100779	ORPHA:90794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0000028	ORPHA:1512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0000175	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0000316	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0000347	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0000358	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0000463	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0000882	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0001387	ORPHA:1512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0001511	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0001762	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0001770	ORPHA:1512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0002119	ORPHA:1512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0004331	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0005280	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0006101	ORPHA:1512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0006660	ORPHA:1512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0007370	ORPHA:1512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0008736	ORPHA:1512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0009882	ORPHA:1512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1512	Crane-Heise syndrome		HP:0100569	ORPHA:1512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000047	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000049	ORPHA:2842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000069	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000078	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000104	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000110	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000269	ORPHA:2842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000286	ORPHA:2842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000347	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000768	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000795	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0000811	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0001638	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0002120	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0004209	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0006443	ORPHA:2842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0006610	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0007598	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0010751	ORPHA:2842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2842	Penoscrotal transposition		HP:0100600	ORPHA:2842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000062	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000822	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0001507	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0002900	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0003351	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0005616	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0008163	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0025380	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0030348	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0031213	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0032330	ORPHA:90795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000040	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000061	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000826	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000858	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000953	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0001007	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0001061	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0003154	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0004322	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0008236	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0008665	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0012411	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0012412	ORPHA:90795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000127	ORPHA:90795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000147	ORPHA:90795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0000771	ORPHA:90795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0001596	ORPHA:90795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0025451	ORPHA:90795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0030088	ORPHA:90795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0002170	ORPHA:90795	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90795	Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency		HP:0010314	ORPHA:90795	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0001298	ORPHA:51188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0003219	ORPHA:51188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0000967	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0001063	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0001249	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0001250	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0001251	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0001290	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0001508	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0002014	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0002071	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0002376	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0003128	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0007256	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0012751	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0012758	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0012841	ORPHA:51188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51188	Ethylmalonic encephalopathy		HP:0012747	ORPHA:51188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276183	Spinocerebellar ataxia type 32		HP:0000027	ORPHA:276183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276183	Spinocerebellar ataxia type 32		HP:0000029	ORPHA:276183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276183	Spinocerebellar ataxia type 32		HP:0001272	ORPHA:276183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276183	Spinocerebellar ataxia type 32		HP:0002073	ORPHA:276183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276183	Spinocerebellar ataxia type 32		HP:0003251	ORPHA:276183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276183	Spinocerebellar ataxia type 32		HP:0100543	ORPHA:276183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0000544	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002013	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002015	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002018	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002020	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002027	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002352	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002579	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003270	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0004326	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0004396	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0007141	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0012850	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0025149	ORPHA:298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0000407	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0000508	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0000597	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0001155	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0001824	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002014	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002460	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002500	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002910	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0002922	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003128	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003200	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003348	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003387	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003388	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003401	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003431	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003448	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003477	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0007108	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0008049	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0009027	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0009830	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0011024	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0012103	ORPHA:298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0000044	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0000815	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0001249	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0001394	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0001403	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0001903	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0003199	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0025461	ORPHA:298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:298	Mitochondrial neurogastrointestinal encephalomyopathy		HP:0000726	ORPHA:298	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000453	ORPHA:280200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0006315	ORPHA:280200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0010644	ORPHA:280200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000252	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000322	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000446	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000601	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001249	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001511	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001622	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0004322	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0010804	ORPHA:280200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000062	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000104	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000175	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000202	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000463	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000486	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000612	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000821	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0000871	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001028	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001250	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001274	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001360	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0001636	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0002099	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0002247	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0002650	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0003196	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0003458	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0008736	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0009800	ORPHA:280200	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0009914	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280200	Microform holoprosencephaly		HP:0030680	ORPHA:280200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0002098	ORPHA:99125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0000961	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001631	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001649	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0002092	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0002875	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0011539	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0011719	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0012378	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0012763	ORPHA:99125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0000980	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001629	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001640	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001643	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001651	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001708	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001719	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001750	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0002033	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0002089	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0002205	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0002240	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0004383	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0004415	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0004887	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0005180	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0005253	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0005949	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0009805	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0011720	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0011721	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0011722	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0030853	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0030918	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0030919	ORPHA:99125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001653	ORPHA:99125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001669	ORPHA:99125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0001680	ORPHA:99125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0011560	ORPHA:99125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99125	Congenital total pulmonary venous return anomaly		HP:0012304	ORPHA:99125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0000478	ORPHA:295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0000504	ORPHA:295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0001511	ORPHA:295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0001541	ORPHA:295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0001639	ORPHA:295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0001789	ORPHA:295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0001873	ORPHA:295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0001903	ORPHA:295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:295	Fetal parvovirus syndrome		HP:0010880	ORPHA:295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33314	Jessner lymphocytic infiltration of the skin		HP:0000989	ORPHA:33314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33314	Jessner lymphocytic infiltration of the skin		HP:0000992	ORPHA:33314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33314	Jessner lymphocytic infiltration of the skin		HP:0004332	ORPHA:33314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33314	Jessner lymphocytic infiltration of the skin		HP:0010783	ORPHA:33314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33314	Jessner lymphocytic infiltration of the skin		HP:0200034	ORPHA:33314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33314	Jessner lymphocytic infiltration of the skin		HP:0200035	ORPHA:33314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0000407	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0001249	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0001744	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0001873	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0001903	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0001928	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0002240	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0002908	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0002910	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0012424	ORPHA:294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0000252	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0000573	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0000648	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0000952	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0000967	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0001250	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0001511	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0002119	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0002514	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294	Fetal cytomegalovirus syndrome		HP:0012115	ORPHA:294	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0012229	ORPHA:297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001882	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002018	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002039	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002315	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002829	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003326	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0011112	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0012378	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0020071	ORPHA:297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000360	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000365	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000505	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000602	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000613	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000708	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000716	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000751	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001262	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001287	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001291	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001308	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001337	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001873	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001974	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002013	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002015	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002311	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002321	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002360	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002487	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003202	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003237	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003418	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003470	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003474	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003496	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0003565	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0004372	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0009763	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0011098	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0011227	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0011392	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0011450	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0012332	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0025258	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0031987	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0032044	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0100543	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:3000047	ORPHA:297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0000709	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001259	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0001637	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002197	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0002910	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0007359	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0010628	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0011441	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0012486	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0012747	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0030196	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0031003	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:297	Tick-borne encephalitis		HP:0031258	ORPHA:297	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0000944	ORPHA:296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0001028	ORPHA:296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002763	ORPHA:296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002797	ORPHA:296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002983	ORPHA:296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0005701	ORPHA:296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0100761	ORPHA:296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0001387	ORPHA:296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0001482	ORPHA:296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002653	ORPHA:296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0000324	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002650	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002664	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002756	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002857	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002967	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0002970	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0003067	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0004936	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0006765	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0006824	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0100242	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0100559	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0100560	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0100764	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:296	Ollier disease		HP:0200042	ORPHA:296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000252	ORPHA:96097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0004322	ORPHA:96097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000028	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000047	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000160	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000233	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000286	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000316	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000343	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000347	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000369	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000400	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000426	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000494	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000670	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000750	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0001156	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0001363	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0001629	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0002342	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0002984	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0003022	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0003196	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0012368	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0100790	ORPHA:96097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000567	ORPHA:96097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0000964	ORPHA:96097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0001651	ORPHA:96097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0009777	ORPHA:96097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96097	Distal duplication 5q syndrome		HP:0011466	ORPHA:96097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0000252	ORPHA:291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0000518	ORPHA:291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0000568	ORPHA:291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0000987	ORPHA:291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0001249	ORPHA:291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0001263	ORPHA:291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0001511	ORPHA:291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0002120	ORPHA:291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:291	Congenital varicella syndrome		HP:0002983	ORPHA:291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000235	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000252	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000407	ORPHA:290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000486	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000501	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000505	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000518	ORPHA:290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000568	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000639	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000944	ORPHA:290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000952	ORPHA:290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0000988	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001249	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001250	ORPHA:290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001252	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001264	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001511	ORPHA:290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001629	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001631	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001643	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001744	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001873	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0001903	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0002167	ORPHA:290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0002240	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0004322	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0004414	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0007703	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0007957	ORPHA:290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0008053	ORPHA:290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:290	Congenital rubella syndrome		HP:0100651	ORPHA:290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293	Congenital herpes simplex virus infection		HP:0000252	ORPHA:293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293	Congenital herpes simplex virus infection		HP:0001511	ORPHA:293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293	Congenital herpes simplex virus infection		HP:0001622	ORPHA:293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293	Congenital herpes simplex virus infection		HP:0002324	ORPHA:293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0000988	ORPHA:292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0000707	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0000737	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001287	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001873	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001945	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0002086	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0025031	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0100806	ORPHA:292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001396	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001399	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001558	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001561	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001622	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001638	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001698	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001789	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001791	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001875	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001882	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001892	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001903	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001974	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0002098	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0002119	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0002202	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0002383	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0002615	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0003073	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0005521	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0011121	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0012115	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0012758	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0012819	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0025116	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0200149	ORPHA:292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0001987	ORPHA:292	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0002045	ORPHA:292	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:292	Congenital enterovirus infection		HP:0004311	ORPHA:292	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001276	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001999	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0002292	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0002510	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0002916	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0008947	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0010864	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0011220	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0011344	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000079	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000311	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000343	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000431	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000478	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000717	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000729	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001274	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001627	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0004209	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0005656	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0007018	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0007020	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0100710	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0100807	ORPHA:96092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000028	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000054	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000126	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000278	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000316	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000347	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000384	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000470	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000592	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000664	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000826	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001250	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001305	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001321	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001636	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001651	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0002650	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0002705	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0002827	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0005781	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0006292	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0010487	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0011466	ORPHA:96092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000154	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000232	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000400	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000463	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000750	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0000767	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001249	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001256	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96092	8p inverted duplication/deletion syndrome		HP:0001263	ORPHA:96092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000414	ORPHA:363958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000447	ORPHA:363958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000750	ORPHA:363958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001252	ORPHA:363958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001263	ORPHA:363958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001999	ORPHA:363958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0100025	ORPHA:363958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000028	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000047	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000119	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000232	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000276	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000286	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000365	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000400	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000411	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000486	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000505	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000508	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000540	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000582	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000708	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000968	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001250	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001256	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001319	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001373	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001382	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001382	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001518	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001627	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001761	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001763	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001848	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002011	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002119	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002342	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002353	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0005656	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0007359	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0008897	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0011182	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0011185	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0011968	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0012433	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0012443	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0012745	ORPHA:363958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000010	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000075	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000076	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000126	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000194	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000238	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000256	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000403	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000426	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000430	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000431	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000519	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000581	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000648	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000729	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000739	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000748	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000767	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000768	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000826	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000957	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000960	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000962	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000964	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001010	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001045	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001054	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001166	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001212	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001274	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001363	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001533	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001596	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001601	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001629	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001631	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001638	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001642	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001647	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002079	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002197	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002205	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002286	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002414	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002650	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002652	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002779	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002808	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0003302	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0003307	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0004942	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0005216	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0006482	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0006813	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0007018	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0007099	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0008064	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0008207	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0008445	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0009130	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0009928	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0010864	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0010945	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0011098	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0011470	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0011822	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0012683	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0012699	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0025268	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0030746	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0100775	ORPHA:363958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000252	ORPHA:363958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000821	ORPHA:363958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0000824	ORPHA:363958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0001028	ORPHA:363958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0002861	ORPHA:363958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363958	17q21.31 microdeletion syndrome		HP:0010788	ORPHA:363958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000207	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000232	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000272	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000316	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000322	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000457	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000494	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000508	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0001643	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0005280	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0012471	ORPHA:46627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0004209	ORPHA:46627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0004220	ORPHA:46627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0006159	ORPHA:46627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000269	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000365	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000486	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0000545	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0001161	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0001263	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0001629	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0001770	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0002360	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0002558	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0004218	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0006335	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0006349	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46627	Char syndrome		HP:0010112	ORPHA:46627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001250	ORPHA:244310	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001252	ORPHA:244310	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001263	ORPHA:244310	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0000365	ORPHA:244310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0002804	ORPHA:244310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0000252	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0000505	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001508	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001892	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001928	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001977	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0002240	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0003186	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0004322	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0011968	ORPHA:244310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0000932	ORPHA:244310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0001251	ORPHA:244310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0002059	ORPHA:244310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0002120	ORPHA:244310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0002401	ORPHA:244310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0007146	ORPHA:244310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244310	RFT1-CDG		HP:0030890	ORPHA:244310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0000407	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0000486	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0000501	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0000541	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0000787	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0000822	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0001072	ORPHA:2833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0001324	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0001376	ORPHA:2833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0001482	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0003011	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0003119	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0004322	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0005978	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0007328	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0008065	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0009830	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0011800	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0100578	ORPHA:2833	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2833	Stiff skin syndrome		HP:0100679	ORPHA:2833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0007407	ORPHA:2834	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000023	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000028	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000218	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000253	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000286	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000316	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000319	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000343	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000369	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000455	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000494	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000670	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000684	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000750	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000767	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000938	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0000973	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001263	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001374	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001476	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001508	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001511	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001537	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001611	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001763	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001788	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001869	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0002645	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0002751	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0002761	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0002812	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0003160	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0003199	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0004322	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0004426	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0004993	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0005272	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0005425	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0006114	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0006191	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0006891	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0007392	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0007457	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0008070	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0008113	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0008897	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0008947	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0009125	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0010838	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0011003	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0025167	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0200141	ORPHA:2834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001305	ORPHA:2834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001320	ORPHA:2834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0001350	ORPHA:2834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0002073	ORPHA:2834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0002133	ORPHA:2834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0011995	ORPHA:2834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome		HP:0010989	ORPHA:2834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2834	Wrinkly skin syndrome	NOT	HP:0002097	ORPHA:2834	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000044	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000164	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000545	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000668	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001251	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001260	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001332	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0006808	ORPHA:289494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000496	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000823	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001337	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0002015	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0002071	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0002307	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0002493	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0004322	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0007240	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0030890	ORPHA:289494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000570	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000640	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000684	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000824	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001250	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001268	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001272	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0001310	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0002075	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0002079	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0002926	ORPHA:289494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000518	ORPHA:289494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0000648	ORPHA:289494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289494	4H leukodystrophy		HP:0031206	ORPHA:289494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0000256	ORPHA:2835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0000271	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0000272	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0000336	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0000337	ORPHA:2835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0000767	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0001252	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0001263	ORPHA:2835	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0001800	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0002164	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0003196	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0004322	ORPHA:2835	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0005280	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0010669	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2835	Pectus excavatum-macrocephaly-dysplastic nails syndrome		HP:0011220	ORPHA:2835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000174	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000177	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000194	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000212	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000238	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000252	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000272	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000286	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000293	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000400	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000463	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000496	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000572	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000648	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0001182	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0001250	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0001263	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0001272	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0001347	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0001371	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0001376	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002119	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002120	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002132	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002205	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002329	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002353	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002521	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0002804	ORPHA:2836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0003196	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0004422	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0006829	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0007366	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0000377	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0010741	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0010864	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0011800	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0011968	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0012398	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0012469	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0100022	ORPHA:2836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2836	PEHO syndrome		HP:0100540	ORPHA:2836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2838	Renal caliceal diverticuli-deafness syndrome		HP:0000077	ORPHA:2838	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2838	Renal caliceal diverticuli-deafness syndrome		HP:0000079	ORPHA:2838	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2838	Renal caliceal diverticuli-deafness syndrome		HP:0000407	ORPHA:2838	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2838	Renal caliceal diverticuli-deafness syndrome		HP:0000072	ORPHA:2838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2838	Renal caliceal diverticuli-deafness syndrome		HP:0000126	ORPHA:2838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2838	Renal caliceal diverticuli-deafness syndrome		HP:0010935	ORPHA:2838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0005775	ORPHA:2839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000062	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000126	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000171	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000175	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000238	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000347	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000377	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000480	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000482	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000612	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0000890	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0001159	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0001591	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0001762	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0002324	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0002414	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0002515	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0002938	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0003083	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0003173	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0003175	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0003312	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0004322	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0005026	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0005613	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0005769	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0006077	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0006492	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0006710	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0006712	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0006713	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0007633	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0008472	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0008551	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0008807	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0008857	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0009100	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0009937	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0012745	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2839	Pelvis-shoulder dysplasia		HP:0100490	ORPHA:2839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0000365	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0000413	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0002644	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0002823	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0002827	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0002983	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0004322	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0004349	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1508	Coxoauricular syndrome		HP:0008551	ORPHA:1508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000003	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000023	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000028	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000126	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000154	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000164	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000174	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000202	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000212	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000256	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000286	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000316	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000322	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000343	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000347	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000365	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000358	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000389	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000431	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000463	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000470	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000486	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000494	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000508	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000520	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000527	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000582	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000592	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000637	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000668	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000767	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000768	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000902	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0000960	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001052	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001156	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001171	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001249	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001522	ORPHA:1507	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001537	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001596	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001629	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001631	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001636	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001641	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001679	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001702	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001770	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0001852	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0002007	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0002205	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0002263	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0002650	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0002714	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0002808	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0003027	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0003042	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0003196	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0003272	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0003422	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0004209	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0004397	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0005048	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0005280	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0006101	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0007598	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0008736	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0008873	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0009882	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0010059	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0010296	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0010297	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0010804	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0010807	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0011069	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0011304	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0011800	ORPHA:1507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0012815	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0100490	ORPHA:1507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1507	Autosomal recessive Robinow syndrome		HP:0100798	ORPHA:1507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0000174	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0000256	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0000358	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0000772	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0001511	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0002007	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0002644	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1506	Thin ribs-tubular bones-dysmorphism syndrome		HP:0003100	ORPHA:1506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001531	ORPHA:488627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000280	ORPHA:488627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001250	ORPHA:488627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001263	ORPHA:488627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000093	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000253	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002120	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002187	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001288	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002465	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0007052	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0007334	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0012213	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0012622	ORPHA:488627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000100	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000407	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000486	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000505	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000592	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000639	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000709	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000718	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0000961	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001260	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001288	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001290	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001344	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001347	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0001970	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002015	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002079	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002119	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002141	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002193	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002367	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0002857	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0006956	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0006989	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0040329	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0100702	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488627	Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome		HP:0100814	ORPHA:488627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0000286	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0000303	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0000445	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0000457	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0001156	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0002812	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0002857	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0003196	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0003307	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0003312	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0004097	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0005687	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0005792	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0008905	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0010049	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0012368	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2831	Rhizomelic dysplasia, Patterson-Lowry type		HP:0100729	ORPHA:2831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0006744	ORPHA:1501	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000080	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000737	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000739	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000819	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000822	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000859	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000975	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0000998	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0001065	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0001324	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0001824	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0001939	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0001962	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0002027	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0002900	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0003118	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0003466	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0004324	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0011748	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0012030	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0025134	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0025269	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0025380	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0025436	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0030078	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0030348	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0500022	ORPHA:1501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1501	Adrenocortical carcinoma		HP:0003110	ORPHA:1501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0001877	ORPHA:288	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0004445	ORPHA:288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0005502	ORPHA:288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0000952	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0001744	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0001878	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0001923	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0002904	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0003265	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0003546	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0004446	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0004447	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0004804	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0006579	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0012378	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0200042	ORPHA:288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0001081	ORPHA:288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0001789	ORPHA:288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0001945	ORPHA:288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0002007	ORPHA:288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0002027	ORPHA:288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0008897	ORPHA:288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:288	Hereditary elliptocytosis		HP:0025143	ORPHA:288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0000962	ORPHA:79503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0001581	ORPHA:79503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0007447	ORPHA:79503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0008064	ORPHA:79503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0001371	ORPHA:79503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0008404	ORPHA:79503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0007460	ORPHA:79503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79503	Ichthyosis hystrix of Curth-Macklin		HP:0011889	ORPHA:79503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000974	ORPHA:287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001027	ORPHA:287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001030	ORPHA:287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001065	ORPHA:287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001073	ORPHA:287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001075	ORPHA:287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002761	ORPHA:287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000938	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001058	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001252	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001324	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002013	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002018	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002020	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0003394	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0003771	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0012378	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0012450	ORPHA:287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000015	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000023	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000139	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000286	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000481	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000978	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0000993	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001063	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001270	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001386	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001537	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001622	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001760	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001762	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001763	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001788	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002035	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002036	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002616	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002650	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002758	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002827	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002829	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002999	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0003010	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0003083	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0003834	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0004872	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0004944	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0004947	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0005294	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0006243	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0007495	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0009763	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0010749	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0010750	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0010754	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0025014	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0025019	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0025509	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0030009	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0031364	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0031653	ORPHA:287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001278	ORPHA:287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001634	ORPHA:287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001653	ORPHA:287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0001704	ORPHA:287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:287	Classical Ehlers-Danlos syndrome		HP:0002315	ORPHA:287	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000164	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000774	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001161	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001231	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001508	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001595	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001597	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001654	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001800	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001829	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002164	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002857	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002983	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0006695	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0008921	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0009882	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0010306	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0011830	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0030680	ORPHA:289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000028	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000039	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000047	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000069	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000077	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000190	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000486	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000668	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000691	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001241	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001511	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001629	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001631	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001651	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001696	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002644	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0006703	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0011065	ORPHA:289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000008	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000072	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000233	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000684	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0000924	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0001249	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002097	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002488	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002750	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0002967	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0005048	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0005561	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0008678	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289	Ellis Van Creveld syndrome		HP:0011362	ORPHA:289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0002073	ORPHA:276193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0001260	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0001272	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0001310	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0001347	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0002066	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0002070	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0002080	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0001288	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0003487	ORPHA:276193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0000467	ORPHA:276193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0000473	ORPHA:276193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0000641	ORPHA:276193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0002342	ORPHA:276193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35		HP:0007024	ORPHA:276193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35	NOT	HP:0000602	ORPHA:276193	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35	NOT	HP:0000639	ORPHA:276193	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:276193	Spinocerebellar ataxia type 35	NOT	HP:0009830	ORPHA:276193	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0002878	ORPHA:280210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0004322	ORPHA:280210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0040288	ORPHA:280210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0000639	ORPHA:280210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0002061	ORPHA:280210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0002171	ORPHA:280210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0006808	ORPHA:280210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0007210	ORPHA:280210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0010864	ORPHA:280210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0012447	ORPHA:280210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001251	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001252	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001260	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001344	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0002421	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0002540	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0004302	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0006511	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001302	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0012043	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0030187	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0031954	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0040330	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0430015	ORPHA:280210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001321	ORPHA:280210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001508	ORPHA:280210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form		HP:0001288	ORPHA:280210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001407	ORPHA:284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001880	ORPHA:284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0003565	ORPHA:284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0010702	ORPHA:284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0000952	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001410	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001903	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001945	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002027	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0003419	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0010741	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0012378	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0025406	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0410019	ORPHA:284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0000107	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0000766	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001824	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002094	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002105	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002315	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0010766	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0011732	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0012735	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0025408	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0030151	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0031292	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0032445	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0100749	ORPHA:284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0000775	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001250	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001251	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001260	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001269	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001409	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001697	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0001737	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002013	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002321	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002381	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002516	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002613	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0002639	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0003468	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0010576	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0011805	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0012062	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0025487	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0040163	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0100016	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284	Alveolar echinococcosis		HP:0100523	ORPHA:284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000015	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000028	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000190	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000271	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000286	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000316	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000411	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000499	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000506	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000670	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000767	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000822	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000912	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000951	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000963	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000978	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000995	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001263	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001634	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001654	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001892	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002107	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002617	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002647	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002900	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0004322	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0005244	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0007495	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0009906	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0010648	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0011029	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0012733	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100543	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100784	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100840	ORPHA:286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000233	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000501	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000520	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001622	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001762	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002093	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002619	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002642	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0004947	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0005294	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0012368	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100585	ORPHA:286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000023	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000047	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000139	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000160	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000164	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000168	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000212	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000230	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000446	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000490	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000508	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000563	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000592	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000615	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000691	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0000704	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001000	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001073	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001373	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001374	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001482	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001537	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001582	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001596	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002076	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002105	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002242	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002321	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002326	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002705	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002758	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0002797	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0004372	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0004937	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0004942	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0004970	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0001382	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0006323	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0007392	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0007900	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0010318	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0010535	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0010719	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0030680	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100545	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100645	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100718	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:286	Vascular Ehlers-Danlos syndrome		HP:0100817	ORPHA:286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0003401	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0004970	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0005293	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0005294	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0010318	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0011003	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0012332	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0012732	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0030880	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0032152	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0100550	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0100645	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0100823	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0400008	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000974	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001063	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001373	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001382	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001760	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002321	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002360	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002645	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002827	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002829	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0003042	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0003326	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001382	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0012378	ORPHA:285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000678	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000716	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000739	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000762	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000963	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000977	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000978	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001065	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001166	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001634	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001763	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002017	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002019	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002024	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002035	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002076	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002758	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0011675	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0012532	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0031607	ORPHA:285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000023	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000144	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000212	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000230	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000286	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000421	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000508	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000563	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000691	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0000987	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001097	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001376	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001482	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0001537	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002020	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002104	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002579	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002616	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002650	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002705	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0002797	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:285	Hypermobile Ehlers-Danlos syndrome		HP:0003019	ORPHA:285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001631	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001654	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001671	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001760	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001762	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002144	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002360	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002650	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002720	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002750	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002808	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0003312	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0003468	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0004467	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0006655	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0006703	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0007385	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0008830	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0009778	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0010109	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0011968	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0030680	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000078	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000079	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000151	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000175	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000389	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000485	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000486	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000488	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000501	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000520	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000639	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000647	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000939	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001274	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001519	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002205	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002715	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0003363	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0005264	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0006709	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0007360	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0010464	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0100022	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0100790	ORPHA:280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000047	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000153	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000159	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000252	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000268	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000286	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000288	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000316	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000322	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000347	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000348	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000358	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000431	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000494	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000668	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001250	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001251	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001252	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001263	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001508	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001511	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001558	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002007	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002162	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002553	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0002714	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0008551	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0009890	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0010864	ORPHA:280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000028	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000077	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000204	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000365	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000508	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000612	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000648	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000679	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000684	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000765	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000776	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000902	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000925	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000958	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0000960	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001028	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001166	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001171	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001177	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280	Wolf-Hirschhorn syndrome		HP:0001362	ORPHA:280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2818	Spastic paraplegia-glaucoma-intellectual disability syndrome		HP:0000501	ORPHA:2818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2818	Spastic paraplegia-glaucoma-intellectual disability syndrome		HP:0001249	ORPHA:2818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2818	Spastic paraplegia-glaucoma-intellectual disability syndrome		HP:0001257	ORPHA:2818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2818	Spastic paraplegia-glaucoma-intellectual disability syndrome		HP:0010550	ORPHA:2818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0000953	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0001025	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0001053	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0001257	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0001288	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0001347	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0002167	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0002353	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2819	Spastic paraplegia-facial-cutaneous lesions syndrome		HP:0010550	ORPHA:2819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000252	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000286	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000308	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000311	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000358	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000431	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0001252	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0001608	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0001620	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0010864	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0011344	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0200046	ORPHA:281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000218	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000316	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000470	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000494	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0001511	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0002650	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0004322	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0200055	ORPHA:281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000023	ORPHA:281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0000384	ORPHA:281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0002757	ORPHA:281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0004348	ORPHA:281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0001382	ORPHA:281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0006101	ORPHA:281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281	Monosomy 5p syndrome		HP:0030680	ORPHA:281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0001029	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0002064	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0003400	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0003693	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0007020	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0007108	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0007141	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2821	Spastic paraplegia-neuropathy-poikiloderma syndrome		HP:0011457	ORPHA:2821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001250	ORPHA:488635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001252	ORPHA:488635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0011344	ORPHA:488635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0000750	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001265	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001321	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001382	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001510	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001999	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0002066	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0002079	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0002141	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0030047	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0031936	ORPHA:488635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0000219	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0000316	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0000445	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0000540	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0000729	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001187	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001272	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001344	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001511	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0001763	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0002069	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0002329	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0003394	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0005280	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0007258	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0008081	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0010510	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0011193	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome		HP:0011968	ORPHA:488635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001256	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001268	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001328	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002079	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002191	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002385	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0003477	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0007141	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0007178	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0007340	ORPHA:2822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000639	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000708	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000712	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000736	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001152	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001251	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001260	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001288	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002015	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002120	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002354	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002540	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0003445	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0003482	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0006913	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0006956	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0007350	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0030455	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0030890	ORPHA:2822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000486	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000505	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000546	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000709	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0000726	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001004	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001250	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001278	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001300	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001513	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0001761	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002071	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0002650	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0003693	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0006827	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0007183	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0009055	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0025058	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0025502	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2822	Autosomal recessive spastic paraplegia type 11		HP:0045007	ORPHA:2822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0000340	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0000347	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0000348	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0000483	ORPHA:2824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0000508	ORPHA:2824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0000639	ORPHA:2824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0000982	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001156	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001166	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001231	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001249	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001257	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001258	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001347	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001348	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0002061	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0002209	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0003189	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0001382	ORPHA:2824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0010579	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2824	Paraplegia-intellectual disability-hyperkeratosis syndrome		HP:0010620	ORPHA:2824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001319	ORPHA:488632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0003323	ORPHA:488632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0003444	ORPHA:488632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0006829	ORPHA:488632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000280	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000750	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001250	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001284	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001315	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001999	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002079	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002093	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002119	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002283	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002518	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002540	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0003119	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0003202	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0011344	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0031165	ORPHA:488632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000158	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000256	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000286	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000337	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000340	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000414	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000574	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000767	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000821	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000939	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001007	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001629	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002045	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002376	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002650	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002705	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002750	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0009826	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0010804	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0011198	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0100288	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0100543	ORPHA:488632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000011	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000028	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000252	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000303	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000343	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000407	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000431	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000470	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000486	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000490	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000582	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000639	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000664	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000717	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000824	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000836	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000878	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0000964	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001500	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001540	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001562	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001642	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0001837	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0002099	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0004691	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0005487	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0007302	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0007957	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0011734	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0012547	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488632	TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome		HP:0030084	ORPHA:488632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2826	Spastic paraplegia-precocious puberty syndrome		HP:0001260	ORPHA:2826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2826	Spastic paraplegia-precocious puberty syndrome		HP:0001348	ORPHA:2826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2826	Spastic paraplegia-precocious puberty syndrome		HP:0002342	ORPHA:2826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2826	Spastic paraplegia-precocious puberty syndrome		HP:0007020	ORPHA:2826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2826	Spastic paraplegia-precocious puberty syndrome		HP:0008185	ORPHA:2826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2826	Spastic paraplegia-precocious puberty syndrome		HP:0010791	ORPHA:2826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002063	ORPHA:2828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000716	ORPHA:2828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000738	ORPHA:2828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000741	ORPHA:2828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0001337	ORPHA:2828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002172	ORPHA:2828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0100660	ORPHA:2828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000551	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000726	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0012760	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000736	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000739	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0001257	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0001332	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0001347	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002014	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002018	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002019	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002067	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002141	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0002578	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0003394	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0004409	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0012332	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0012452	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0025269	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0030014	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0040307	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0100543	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0100785	ORPHA:2828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000651	ORPHA:2828	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000713	ORPHA:2828	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0000727	ORPHA:2828	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2828	Young-onset Parkinson disease		HP:0100710	ORPHA:2828	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002470	ORPHA:314978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0000486	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0001152	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0001270	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0001320	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0001321	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002078	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002080	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002312	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002317	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002345	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002359	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0002464	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia		HP:0008935	ORPHA:314978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia	NOT	HP:0001249	ORPHA:314978	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:314978	X-linked non progressive cerebellar ataxia	NOT	HP:0003487	ORPHA:314978	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0000365	ORPHA:276198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0001251	ORPHA:276198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0001260	ORPHA:276198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002070	ORPHA:276198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002078	ORPHA:276198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0000514	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0000622	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0001308	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0001310	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0001288	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002380	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0003202	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0003487	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0007001	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0012473	ORPHA:276198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0000508	ORPHA:276198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0001347	ORPHA:276198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0000651	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002015	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002076	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002080	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002321	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002346	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002378	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0002607	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0007018	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276198	Spinocerebellar ataxia type 36		HP:0045084	ORPHA:276198	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0012382	ORPHA:99104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0031297	ORPHA:99104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0001962	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0002875	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0003546	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0010772	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0012378	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0031634	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0031664	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0031687	ORPHA:99104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0002092	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0002094	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0002326	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0005115	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0005133	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0011675	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0011710	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0030718	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0031972	ORPHA:99104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0000961	ORPHA:99104	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0001279	ORPHA:99104	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0001297	ORPHA:99104	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0001708	ORPHA:99104	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0002090	ORPHA:99104	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0002718	ORPHA:99104	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99104	Atrial septal defect, coronary sinus type		HP:0005317	ORPHA:99104	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0012382	ORPHA:99105	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0001962	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0002875	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0003546	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0010772	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0012378	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0031546	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0031663	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0031664	ORPHA:99105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0001692	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0002092	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0002094	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0004749	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0004755	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0005110	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0005115	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0005133	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0005180	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0006699	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0011700	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0011705	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0011712	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0011716	ORPHA:99105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0001297	ORPHA:99105	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0001635	ORPHA:99105	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0001907	ORPHA:99105	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99105	Atrial septal defect, sinus venosus type		HP:0006536	ORPHA:99105	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001653	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001712	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001962	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0002205	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0002875	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0004927	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0005133	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0005180	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0011705	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0011712	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0012248	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0012378	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0031595	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0031658	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0031662	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0031664	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0031687	ORPHA:99106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0000961	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001279	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001508	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001635	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001678	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001694	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0001907	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0002092	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0002094	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0002105	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0002789	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0002795	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0003546	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0004749	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0005110	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0006536	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0012398	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0030718	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0031295	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0100759	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99106	Atrial septal defect, ostium primum type		HP:0100760	ORPHA:99106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0000093	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0000112	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0000407	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0001249	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0001257	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0001288	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0001347	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0002167	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0010550	ORPHA:2820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0000822	ORPHA:2820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0003510	ORPHA:2820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2820	Spastic paraplegia-nephritis-deafness syndrome		HP:0004209	ORPHA:2820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000486	ORPHA:233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000496	ORPHA:233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000657	ORPHA:233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0009921	ORPHA:233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0012246	ORPHA:233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0012745	ORPHA:233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000407	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000463	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000490	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000542	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000581	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000634	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0002162	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0005640	ORPHA:233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000086	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000175	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000232	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000252	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000324	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000347	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000365	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000384	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000402	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000431	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000465	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000470	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000482	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000508	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000526	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000567	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000612	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000615	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000639	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000643	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000646	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001053	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001156	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001177	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001199	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001250	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001263	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001357	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0001762	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0002984	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0003202	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0003298	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0003312	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0003974	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0007400	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0007766	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0007818	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0007990	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0000377	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0009601	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0011365	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0011386	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0012385	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0012732	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0025186	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0030680	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0031705	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:233	Duane retraction syndrome		HP:0100274	ORPHA:233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0004870	ORPHA:232	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001878	ORPHA:232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0002719	ORPHA:232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0012531	ORPHA:232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0000488	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0000939	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0000952	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001743	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001891	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001894	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001923	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001974	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0002754	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0010885	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0011981	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0012622	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0100749	ORPHA:232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0000707	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001081	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001406	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0002092	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0002140	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0002597	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0003259	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0008282	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0011886	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0011904	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0012418	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0025326	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0025435	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0031090	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0034336	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0200023	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0200042	ORPHA:232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001931	ORPHA:232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0001935	ORPHA:232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:232	Sickle cell anemia		HP:0005518	ORPHA:232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000294	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000340	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000347	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000358	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000403	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000411	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000508	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000581	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000964	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001508	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001609	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001620	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001773	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001852	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002093	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002209	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002213	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002719	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002750	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0004209	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0005280	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000252	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000316	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000506	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001249	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001511	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0004322	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0009601	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0009602	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0009891	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0011304	ORPHA:235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000028	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000047	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000055	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000176	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000260	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000270	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000275	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000286	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0005338	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0007018	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0008897	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0009738	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0012758	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0200055	ORPHA:235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000126	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000164	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000218	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000238	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000365	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000486	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000518	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000545	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000613	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000639	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000678	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000684	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000736	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000750	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000767	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000829	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000958	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000960	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000965	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001000	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001156	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001231	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001250	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001252	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001328	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001363	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001627	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001770	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001800	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001840	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001873	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001874	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001903	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002013	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002019	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002020	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002024	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002025	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002028	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002035	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002099	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002360	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002650	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0003298	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0001382	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0007370	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0008872	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0030680	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:5200060	ORPHA:235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000154	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000485	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000568	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000612	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0000824	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002664	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0002665	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:235	Dubowitz syndrome		HP:0006721	ORPHA:235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0000952	ORPHA:234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0001080	ORPHA:234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0001392	ORPHA:234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0001928	ORPHA:234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0001945	ORPHA:234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0002027	ORPHA:234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0002240	ORPHA:234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0002908	ORPHA:234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0004295	ORPHA:234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0012086	ORPHA:234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:234	Dubin-Johnson syndrome		HP:0012378	ORPHA:234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280224	Pelizaeus-Merzbacher disease, transitional form		HP:0000639	ORPHA:280224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280224	Pelizaeus-Merzbacher disease, transitional form		HP:0003429	ORPHA:280224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280224	Pelizaeus-Merzbacher disease, transitional form		HP:0001285	ORPHA:280224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280224	Pelizaeus-Merzbacher disease, transitional form		HP:0002342	ORPHA:280224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280224	Pelizaeus-Merzbacher disease, transitional form		HP:0010864	ORPHA:280224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0000988	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0000989	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0001369	ORPHA:231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0001371	ORPHA:231	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0001376	ORPHA:231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0001482	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0002014	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0002017	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0008066	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0011134	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0100326	ORPHA:231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0100658	ORPHA:231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0100758	ORPHA:231	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0100838	ORPHA:231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231	Dracunculiasis		HP:0200042	ORPHA:231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001278	ORPHA:230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001488	ORPHA:230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0011979	ORPHA:230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0012384	ORPHA:230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001279	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001315	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001903	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001943	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0002360	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0003138	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0003259	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0009020	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0012378	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0012877	ORPHA:230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0000017	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0000622	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001252	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0001944	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0002013	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0002014	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0002045	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0002094	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0002321	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0003115	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0012670	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0100749	ORPHA:230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0000842	ORPHA:230	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:230	Dopamine beta-hydroxylase deficiency		HP:0000855	ORPHA:230	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0000238	ORPHA:2807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0000505	ORPHA:2807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0001250	ORPHA:2807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0001276	ORPHA:2807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0002664	ORPHA:2807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0004374	ORPHA:2807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0012639	ORPHA:2807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0100543	ORPHA:2807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2807	Papilloma of choroid plexus		HP:0200022	ORPHA:2807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2808	Laryngeal abductor paralysis		HP:0001601	ORPHA:2808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2808	Laryngeal abductor paralysis		HP:0002093	ORPHA:2808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0003323	ORPHA:399096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0009053	ORPHA:399096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0001288	ORPHA:399096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0002515	ORPHA:399096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0003552	ORPHA:399096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0009046	ORPHA:399096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0030234	ORPHA:399096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0003693	ORPHA:399096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0003707	ORPHA:399096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0008997	ORPHA:399096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0009073	ORPHA:399096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy		HP:0003201	ORPHA:399096	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:399096	Distal anoctaminopathy	NOT	HP:0009049	ORPHA:399096	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0000311	ORPHA:2812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0000768	ORPHA:2812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0000962	ORPHA:2812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0001072	ORPHA:2812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0001182	ORPHA:2812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0001510	ORPHA:2812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0002093	ORPHA:2812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0002230	ORPHA:2812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0004322	ORPHA:2812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0006596	ORPHA:2812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0006610	ORPHA:2812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2812	Parana hard skin syndrome		HP:0007440	ORPHA:2812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0000135	ORPHA:2815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0000407	ORPHA:2815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0000505	ORPHA:2815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0000518	ORPHA:2815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0000639	ORPHA:2815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0001251	ORPHA:2815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0001288	ORPHA:2815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0001347	ORPHA:2815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0002313	ORPHA:2815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0004322	ORPHA:2815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0004374	ORPHA:2815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0007328	ORPHA:2815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2815	Spastic paraparesis-deafness syndrome		HP:0100022	ORPHA:2815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0200146	ORPHA:229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0001640	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0001643	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0001659	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0001677	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0002616	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0002875	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0004933	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0004959	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0005162	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0012499	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0012763	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0100749	ORPHA:229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0000965	ORPHA:229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0001297	ORPHA:229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0002647	ORPHA:229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0004944	ORPHA:229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0004950	ORPHA:229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229	Familial aortic dissection		HP:0012163	ORPHA:229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0000639	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0000750	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001251	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001256	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001263	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0006808	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0011203	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0031936	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0040330	ORPHA:280219	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001252	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001257	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001285	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001332	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0002167	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0002305	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0002346	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0001288	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0002421	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0007256	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0007377	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0008936	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0025336	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0030187	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0100543	ORPHA:280219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0002071	ORPHA:280219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0002310	ORPHA:280219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280219	Pelizaeus-Merzbacher disease, classic form		HP:0031954	ORPHA:280219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226	Dihydropteridine reductase deficiency		HP:0000252	ORPHA:226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226	Dihydropteridine reductase deficiency		HP:0001249	ORPHA:226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226	Dihydropteridine reductase deficiency		HP:0001263	ORPHA:226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226	Dihydropteridine reductase deficiency		HP:0002015	ORPHA:226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000048	ORPHA:227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000119	ORPHA:227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0100599	ORPHA:227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000047	ORPHA:227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0002023	ORPHA:227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0008706	ORPHA:227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0030275	ORPHA:227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0100600	ORPHA:227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000023	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000028	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000039	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000073	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000075	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0000085	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0001627	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0001631	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0002836	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0003172	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0004712	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0008669	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0010475	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0011024	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0011140	ORPHA:227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0002650	ORPHA:227	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0002937	ORPHA:227	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0003316	ORPHA:227	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0004792	ORPHA:227	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0005223	ORPHA:227	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227	Diphallia		HP:0009777	ORPHA:227	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:222	Erosive pustular dermatosis of the scalp		HP:0001595	ORPHA:222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:222	Erosive pustular dermatosis of the scalp		HP:0004552	ORPHA:222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:222	Erosive pustular dermatosis of the scalp		HP:0010783	ORPHA:222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:222	Erosive pustular dermatosis of the scalp		HP:0200039	ORPHA:222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:222	Erosive pustular dermatosis of the scalp		HP:0200041	ORPHA:222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001824	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002093	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002205	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002206	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002207	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002747	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002829	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002910	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0003236	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0003458	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0006530	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0011362	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0012378	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0012544	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0025435	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0025508	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0025535	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0034140	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0034141	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0040324	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0100614	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0200034	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0200042	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0000992	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001029	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001596	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001618	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001658	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0000492	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0000969	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002960	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0003325	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0003326	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0003457	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0003701	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0009071	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0010783	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0100539	ORPHA:221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0000934	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0000958	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0000988	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0000989	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001041	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001063	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001252	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001369	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001597	ORPHA:221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001701	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001879	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0001945	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002015	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002092	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002633	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002664	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0002665	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0003002	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0008065	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0008872	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0011675	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0011703	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0012819	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0025536	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0030078	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0030880	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0033033	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0033554	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0034105	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0034139	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0034142	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0034152	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0100585	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0100658	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0100723	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0100758	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0430033	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:6000006	ORPHA:221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221	Dermatomyositis		HP:0010765	ORPHA:221	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0004322	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0011106	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0011968	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0001263	ORPHA:223	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0001561	ORPHA:223	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0010677	ORPHA:223	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0009806	ORPHA:223	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0003158	ORPHA:223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0003228	ORPHA:223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0004906	ORPHA:223	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0001508	ORPHA:223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0001945	ORPHA:223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0001959	ORPHA:223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0002017	ORPHA:223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0002019	ORPHA:223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0002039	ORPHA:223	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0000009	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0000072	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0000083	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0001250	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:223	Arginine vasopressin resistance		HP:0001510	ORPHA:223	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0003134	ORPHA:280234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0003429	ORPHA:280234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0007108	ORPHA:280234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0011096	ORPHA:280234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0000762	ORPHA:280234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0001251	ORPHA:280234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0001288	ORPHA:280234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0007020	ORPHA:280234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0000648	ORPHA:280234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0001317	ORPHA:280234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0002342	ORPHA:280234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0002478	ORPHA:280234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0002540	ORPHA:280234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome		HP:0012758	ORPHA:280234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280234	Null syndrome	NOT	HP:0000639	ORPHA:280234	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:220	Denys-Drash syndrome		HP:0000037	ORPHA:220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220	Denys-Drash syndrome		HP:0000093	ORPHA:220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220	Denys-Drash syndrome		HP:0000100	ORPHA:220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220	Denys-Drash syndrome		HP:0000112	ORPHA:220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220	Denys-Drash syndrome		HP:0002667	ORPHA:220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220	Denys-Drash syndrome		HP:0000822	ORPHA:220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220	Denys-Drash syndrome		HP:0000133	ORPHA:220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0002936	ORPHA:399081	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0003458	ORPHA:399081	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0006466	ORPHA:399081	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0009005	ORPHA:399081	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0009063	ORPHA:399081	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0001430	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0002166	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0001288	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0003376	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0006844	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0006937	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0008954	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0009031	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0040081	ORPHA:399081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0003438	ORPHA:399081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0002505	ORPHA:399081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:399081	KLHL9-related early-onset distal myopathy		HP:0003477	ORPHA:399081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000028	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000298	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000343	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000369	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000377	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000431	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000457	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000506	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000581	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0002553	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0008577	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0009738	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0010720	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0010781	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0045075	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0100024	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0100679	ORPHA:178303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000135	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000164	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000252	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000327	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000470	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0001263	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0001376	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0001852	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0006610	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0100490	ORPHA:178303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000176	ORPHA:178303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0000653	ORPHA:178303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0001363	ORPHA:178303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0005288	ORPHA:178303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178303	8q22.1 microdeletion syndrome		HP:0006101	ORPHA:178303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0002312	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0001288	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0002936	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0003376	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0003458	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0003805	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0008180	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0008954	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0009005	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0009031	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0009063	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0009473	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0012548	ORPHA:399086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0001171	ORPHA:399086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy		HP:0009073	ORPHA:399086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399086	HNRNPA1-related adult-onset distal myopathy	NOT	HP:0001638	ORPHA:399086	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000164	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000256	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000365	ORPHA:2801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000648	ORPHA:2801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000768	ORPHA:2801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000822	ORPHA:2801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000889	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000939	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0000995	ORPHA:2801	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0001482	ORPHA:2801	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0002149	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0002757	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0004322	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0004437	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0006487	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0007703	ORPHA:2801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2801	Juvenile Paget disease		HP:0100670	ORPHA:2801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001251	ORPHA:2802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001903	ORPHA:2802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0002066	ORPHA:2802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0002167	ORPHA:2802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0012187	ORPHA:2802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0031936	ORPHA:2802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0000486	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0000639	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0000750	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001260	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001347	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001348	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001924	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0002172	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0002194	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0004840	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0011273	ORPHA:2802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0000717	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001252	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001272	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001310	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001510	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0002075	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0004447	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0020081	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0034499	ORPHA:2802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0000028	ORPHA:2802	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0000716	ORPHA:2802	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001250	ORPHA:2802	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0001992	ORPHA:2802	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0100543	ORPHA:2802	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2802	X-linked sideroblastic anemia and spinocerebellar ataxia		HP:0100753	ORPHA:2802	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0000176	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0000316	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0000455	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0000494	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0000506	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0001061	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0001137	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0001257	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0001263	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0001761	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0001763	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0001840	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0002069	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0002967	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0002986	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0003022	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0003042	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0005280	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0006293	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0010809	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0011220	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0012385	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0030084	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0100037	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2804	W syndrome		HP:0100268	ORPHA:2804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000708	ORPHA:2806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001268	ORPHA:2806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001336	ORPHA:2806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000716	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000726	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000737	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000738	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000746	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001250	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001254	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001288	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001332	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0002360	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0002371	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0010856	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0010856	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0012332	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0012424	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0012444	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0012672	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0030891	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0031358	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0033044	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0430088	ORPHA:2806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000572	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0000573	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001085	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001251	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0001257	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0002071	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0002119	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0012229	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0012708	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0012709	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:0100660	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2806	Subacute sclerosing leukoencephalitis		HP:6000397	ORPHA:2806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:219	Delta-sarcoglycan-related limb-girdle muscular dystrophy R6		HP:0002362	ORPHA:219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:219	Delta-sarcoglycan-related limb-girdle muscular dystrophy R6		HP:0003691	ORPHA:219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:219	Delta-sarcoglycan-related limb-girdle muscular dystrophy R6		HP:0008948	ORPHA:219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:219	Delta-sarcoglycan-related limb-girdle muscular dystrophy R6		HP:0008956	ORPHA:219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:219	Delta-sarcoglycan-related limb-girdle muscular dystrophy R6		HP:0009055	ORPHA:219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:219	Delta-sarcoglycan-related limb-girdle muscular dystrophy R6		HP:0010628	ORPHA:219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0000989	ORPHA:218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001034	ORPHA:218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001597	ORPHA:218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0008410	ORPHA:218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0045059	ORPHA:218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0200016	ORPHA:218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0000498	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0000982	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001000	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001072	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001097	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001595	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001808	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0005212	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0010610	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0010612	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0031288	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:6001074	ORPHA:218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0000716	ORPHA:218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001249	ORPHA:218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0001250	ORPHA:218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0007302	ORPHA:218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0011859	ORPHA:218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0012733	ORPHA:218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:218	Darier disease		HP:0200037	ORPHA:218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0005306	ORPHA:168984	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0031487	ORPHA:168984	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0001052	ORPHA:168984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0001528	ORPHA:168984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0001548	ORPHA:168984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0100764	ORPHA:168984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0000324	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0001004	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0001508	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0002619	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0004099	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0012721	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0100553	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0100554	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0100555	ORPHA:168984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0000098	ORPHA:168984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0000767	ORPHA:168984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0000774	ORPHA:168984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome		HP:0003005	ORPHA:168984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168984	CLAPO syndrome	NOT	HP:0001249	ORPHA:168984	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0000639	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0000666	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0001252	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0000011	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0000316	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0000490	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0001268	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0001273	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0001288	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0001347	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0001510	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0002061	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0002167	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0002197	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0002313	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0001288	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0002376	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0002540	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0003429	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0003487	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0007413	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0010936	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0011342	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0011343	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0011800	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0030784	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0030890	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0032044	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280229	Pelizaeus-Merzbacher disease in female carriers		HP:0032588	ORPHA:280229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0000545	ORPHA:215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0000662	ORPHA:215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0007663	ORPHA:215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0030469	ORPHA:215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0000486	ORPHA:215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0000639	ORPHA:215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0030638	ORPHA:215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0030639	ORPHA:215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0000540	ORPHA:215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0007984	ORPHA:215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0030483	ORPHA:215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0031705	ORPHA:215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0000551	ORPHA:215	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0007703	ORPHA:215	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:215	Congenital stationary night blindness		HP:0030329	ORPHA:215	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0000787	ORPHA:214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0000790	ORPHA:214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0003131	ORPHA:214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0004337	ORPHA:214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0000083	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0000822	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0002017	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0002149	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0012088	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0012405	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0030157	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0033067	ORPHA:214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0002150	ORPHA:214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:214	Cystinuria		HP:0003149	ORPHA:214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0000238	ORPHA:217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0000256	ORPHA:217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0000269	ORPHA:217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0001305	ORPHA:217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0002691	ORPHA:217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0001321	ORPHA:217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0002007	ORPHA:217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0002198	ORPHA:217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0005445	ORPHA:217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0006817	ORPHA:217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0010952	ORPHA:217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0011427	ORPHA:217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0000175	ORPHA:217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0001249	ORPHA:217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0001270	ORPHA:217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0002084	ORPHA:217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0002516	ORPHA:217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0007370	ORPHA:217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0000639	ORPHA:217	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217	Isolated Dandy-Walker malformation		HP:0002078	ORPHA:217	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000597	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000602	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0001596	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0001804	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0001812	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0002300	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0002381	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0003198	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0010529	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0010547	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0012246	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0200037	ORPHA:257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000508	ORPHA:257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0000682	ORPHA:257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0004334	ORPHA:257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0008065	ORPHA:257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0200034	ORPHA:257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0003473	ORPHA:257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:257	Epidermolysis bullosa simplex with muscular dystrophy		HP:0012378	ORPHA:257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:256	Early-onset generalized limb-onset dystonia		HP:0001276	ORPHA:256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:256	Early-onset generalized limb-onset dystonia		HP:0001288	ORPHA:256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:256	Early-onset generalized limb-onset dystonia		HP:0001608	ORPHA:256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:256	Early-onset generalized limb-onset dystonia		HP:0003011	ORPHA:256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:256	Early-onset generalized limb-onset dystonia		HP:0100022	ORPHA:256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000098	ORPHA:300373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000845	ORPHA:300373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000870	ORPHA:300373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0012503	ORPHA:300373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0030269	ORPHA:300373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000280	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000975	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001072	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0002591	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0002893	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0004924	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0008283	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0010535	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0025163	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0025267	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0031098	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0031418	ORPHA:300373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000135	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000699	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000823	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000873	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000924	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000956	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001123	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001176	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001250	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001251	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001626	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001833	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0002315	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0003270	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0011748	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0012505	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0040075	ORPHA:300373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0000707	ORPHA:300373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300373	X-linked acrogigantism		HP:0001249	ORPHA:300373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001875	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001903	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002066	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002080	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002119	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002120	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002197	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002209	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002293	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002299	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002562	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002705	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002719	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002750	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002828	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002860	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0002942	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0003079	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0003139	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0006297	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0006538	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0006970	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007034	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007256	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007266	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007381	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007485	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007495	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007587	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0007633	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0008064	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0008386	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0008391	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0008619	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0009830	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0010551	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0011001	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0012760	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:4000007	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0025548	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0045055	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0100275	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0410219	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000028	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000133	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000252	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000278	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000280	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000286	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000316	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000320	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000411	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000482	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000483	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000486	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000509	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000519	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000545	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000546	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000565	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000601	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000608	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000613	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000639	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000656	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000670	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000938	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000958	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000964	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0000992	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001097	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001197	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001217	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001257	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001260	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001263	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001265	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001276	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001290	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001338	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001363	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001373	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001511	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001537	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001598	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001618	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001629	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001638	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001807	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001808	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33364	Trichothiodystrophy		HP:0001809	ORPHA:33364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0000958	ORPHA:248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0001231	ORPHA:248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0002213	ORPHA:248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0006323	ORPHA:248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0008388	ORPHA:248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0000685	ORPHA:248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0000966	ORPHA:248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0001595	ORPHA:248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0001596	ORPHA:248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248	Autosomal recessive hypohidrotic ectodermal dysplasia		HP:0006482	ORPHA:248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0010734	ORPHA:249	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000929	ORPHA:249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002797	ORPHA:249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0003330	ORPHA:249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0009121	ORPHA:249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0040064	ORPHA:249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000277	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000326	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002148	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002653	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002748	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002753	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002756	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002823	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0003155	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0005731	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0006487	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0010657	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0010668	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0011821	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0031955	ORPHA:249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000772	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000889	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0001288	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002650	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002696	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002749	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002812	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002818	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002992	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0031095	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0003319	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0004302	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0004322	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0006316	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0009911	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0012294	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0040071	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0040163	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0100559	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0100712	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0430000	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0430022	ORPHA:249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000138	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000365	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000572	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000818	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000819	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000836	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0000845	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002669	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0002890	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0003072	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0003118	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0003401	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0005605	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0007565	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0010465	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0010514	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0010788	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0030428	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:249	Fibrous dysplasia of bone		HP:0100013	ORPHA:249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000389	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000403	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001742	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0002257	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0002643	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0003251	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0005425	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0011109	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0011947	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0012206	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0031245	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0032016	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0100582	ORPHA:244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000119	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000365	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000405	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000750	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000924	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001217	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001627	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001696	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0002011	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0002110	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0006536	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0008222	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0011274	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0011617	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0025177	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0030680	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0030828	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0031456	ORPHA:244	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0032543	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0100750	ORPHA:244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000238	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0000510	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001669	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001719	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001746	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0001748	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0002119	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0002566	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0002878	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0005301	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0010772	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0011535	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0011539	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244	Primary ciliary dyskinesia		HP:0025576	ORPHA:244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000133	ORPHA:243	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0008209	ORPHA:243	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000144	ORPHA:243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000786	ORPHA:243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000823	ORPHA:243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000837	ORPHA:243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0008214	ORPHA:243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0009888	ORPHA:243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000938	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0002225	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0002750	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0004349	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0005625	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0008684	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0010311	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0010464	ORPHA:243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000365	ORPHA:243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000869	ORPHA:243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0001939	ORPHA:243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0004322	ORPHA:243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0000252	ORPHA:243	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0001166	ORPHA:243	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0001251	ORPHA:243	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis		HP:0002206	ORPHA:243	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:243	46,XX gonadal dysgenesis	NOT	HP:0000062	ORPHA:243	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000272	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000347	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000358	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000378	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000494	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000625	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0002558	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0002984	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0003022	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0007477	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0007651	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0008551	ORPHA:246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000175	ORPHA:246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000370	ORPHA:246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000405	ORPHA:246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0006101	ORPHA:246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0030680	ORPHA:246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0100335	ORPHA:246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0100490	ORPHA:246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:246	Postaxial acrofacial dysostosis		HP:0000486	ORPHA:246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000327	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000347	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000365	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000494	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000750	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0002652	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0009601	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0010669	ORPHA:245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000154	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000174	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000175	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000413	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000508	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000652	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0001387	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0002093	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0002984	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0005105	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0006501	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0007776	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0008551	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0100840	ORPHA:245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000122	ORPHA:245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0000358	ORPHA:245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0001199	ORPHA:245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0002814	ORPHA:245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0009829	ORPHA:245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0030680	ORPHA:245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:245	Nager syndrome		HP:0100335	ORPHA:245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0000431	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0000944	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0001156	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0001191	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0001387	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0001804	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002644	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002818	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002823	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002970	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002982	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002983	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002984	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002986	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002992	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0003022	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0003027	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0003031	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0031095	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0003067	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0003272	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0004209	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0005019	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0005280	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0005736	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0005930	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0006248	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0006443	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0006459	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0008873	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0010579	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0010624	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0040071	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0100777	ORPHA:240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002683	ORPHA:240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0002857	ORPHA:240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240	Léri-Weill dyschondrosteosis		HP:0003042	ORPHA:240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228277	Familial anetoderma		HP:0200034	ORPHA:228277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228277	Familial anetoderma		HP:0002705	ORPHA:228277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228277	Familial anetoderma		HP:0002761	ORPHA:228277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228277	Familial anetoderma		HP:0002938	ORPHA:228277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228277	Familial anetoderma		HP:0002992	ORPHA:228277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228277	Familial anetoderma		HP:0040079	ORPHA:228277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:242	46,XY complete gonadal dysgenesis		HP:0000037	ORPHA:242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:242	46,XY complete gonadal dysgenesis		HP:0000044	ORPHA:242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:242	46,XY complete gonadal dysgenesis		HP:0000147	ORPHA:242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:242	46,XY complete gonadal dysgenesis		HP:0008715	ORPHA:242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0000365	ORPHA:241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0000992	ORPHA:241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0001034	ORPHA:241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0001053	ORPHA:241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0001480	ORPHA:241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0004322	ORPHA:241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0005590	ORPHA:241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0007565	ORPHA:241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:241	Dyschromatosis universalis hereditaria		HP:0012733	ORPHA:241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001249	ORPHA:599373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001250	ORPHA:599373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001263	ORPHA:599373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0011185	ORPHA:599373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0000729	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0000750	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0000752	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001251	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001252	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001337	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001344	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0002123	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0002376	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0002384	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0002521	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0002540	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0006989	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0010819	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0010841	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0011097	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0011153	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0011203	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0012469	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0012762	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0200134	ORPHA:599373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001257	ORPHA:599373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0001332	ORPHA:599373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0002510	ORPHA:599373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0007334	ORPHA:599373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0012448	ORPHA:599373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:599373	STXBP1-related encephalopathy		HP:0100660	ORPHA:599373	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0011763	ORPHA:300385	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0000870	ORPHA:300385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0002315	ORPHA:300385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0003154	ORPHA:300385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0006767	ORPHA:300385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0008291	ORPHA:300385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0100836	ORPHA:300385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0007663	ORPHA:300385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0007987	ORPHA:300385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0012377	ORPHA:300385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0012505	ORPHA:300385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0040075	ORPHA:300385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0000365	ORPHA:300385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0000845	ORPHA:300385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0001251	ORPHA:300385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0010514	ORPHA:300385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0011442	ORPHA:300385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0011760	ORPHA:300385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0100561	ORPHA:300385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0000873	ORPHA:300385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0011759	ORPHA:300385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300385	Pituitary carcinoma		HP:0011762	ORPHA:300385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0012363	ORPHA:263494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0001315	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0001324	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0001644	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0001763	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0002187	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0002401	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0002910	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0003487	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0003560	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0003749	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0003805	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0008331	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0008981	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263494	DPM3-CDG		HP:0100749	ORPHA:263494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0011354	ORPHA:167635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0031047	ORPHA:167635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0200034	ORPHA:167635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0000271	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0000464	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0001072	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0001155	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002015	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002056	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002829	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002973	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0003198	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0003236	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0003701	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0011838	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0025512	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0030053	ORPHA:167635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0000077	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0000160	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0000989	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0001250	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0001298	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0001626	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002020	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002088	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002460	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002875	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0003326	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0008509	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0011024	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0011805	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0030178	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0030880	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0100771	ORPHA:167635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0001259	ORPHA:167635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0001297	ORPHA:167635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0002326	ORPHA:167635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0006704	ORPHA:167635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0006775	ORPHA:167635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema		HP:0030966	ORPHA:167635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:167635	Scleromyxedema	NOT	HP:0002926	ORPHA:167635	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0010541	ORPHA:357225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0000290	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0000519	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0001250	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0001263	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0002171	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0006889	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0006970	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0030455	ORPHA:357225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0000252	ORPHA:357225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0001298	ORPHA:357225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0001629	ORPHA:357225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0001631	ORPHA:357225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0002650	ORPHA:357225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0007663	ORPHA:357225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357225	Primary non-essential cutis verticis gyrata		HP:0010562	ORPHA:357225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0000365	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0000389	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0000988	ORPHA:33355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0001508	ORPHA:33355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0001824	ORPHA:33355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0001874	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0001882	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0001903	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0001944	ORPHA:33355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0001945	ORPHA:33355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0002014	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0002024	ORPHA:33355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0002205	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0003287	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0004313	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0004430	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0005374	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0010515	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0100806	ORPHA:33355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33355	Reticular dysgenesis		HP:0200042	ORPHA:33355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000039	ORPHA:237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000047	ORPHA:237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000076	ORPHA:237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0012732	ORPHA:237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000010	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000020	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000041	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000048	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0000054	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0001153	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0001543	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0002023	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0003244	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0003762	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0008635	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0008665	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0008706	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0008743	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0010447	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0012227	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0012531	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0012583	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0025407	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0025489	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0100518	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:237	Duplication of urethra		HP:0100519	ORPHA:237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000248	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000252	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000316	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000400	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000411	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000470	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000490	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000494	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000615	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000678	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0000960	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0001156	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0001249	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0001263	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0001800	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0001804	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0002650	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0002714	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0002808	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0004209	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0005105	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0006610	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0007477	ORPHA:236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0007598	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0011079	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0100335	ORPHA:236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:236	Trisomy 9p syndrome		HP:0100798	ORPHA:236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002656	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003026	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003090	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003183	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003272	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003274	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003368	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003510	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003690	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0004568	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0005106	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0006429	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0008786	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0008905	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0010306	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0010864	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0031233	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0040163	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0100255	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000750	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000752	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001256	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001285	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001347	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001377	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001538	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002359	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002465	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002540	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002747	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002788	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002812	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002857	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003028	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003066	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003311	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003467	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003698	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0004242	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0006633	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0031987	ORPHA:239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease	NOT	HP:0000365	ORPHA:239	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease	NOT	HP:0007957	ORPHA:239	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease	NOT	HP:0012379	ORPHA:239	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001249	ORPHA:239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001508	ORPHA:239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002651	ORPHA:239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0003521	ORPHA:239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000252	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000280	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000470	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000768	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000885	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000925	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000926	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0000946	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001270	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0001288	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:239	Dyggve-Melchior-Clausen disease		HP:0002652	ORPHA:239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228240	Elastoderma		HP:0200034	ORPHA:228240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228240	Elastoderma		HP:0200036	ORPHA:228240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228240	Elastoderma		HP:0100963	ORPHA:228240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228240	Elastoderma		HP:0000964	ORPHA:228240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228240	Elastoderma		HP:0001055	ORPHA:228240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228240	Elastoderma		HP:0000973	ORPHA:228240	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:228240	Elastoderma		HP:0100678	ORPHA:228240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0003027	ORPHA:97360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0004322	ORPHA:97360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000316	ORPHA:97360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001518	ORPHA:97360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0003086	ORPHA:97360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0003241	ORPHA:97360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0005011	ORPHA:97360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000028	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000046	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000054	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000059	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000060	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000126	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000187	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000202	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000207	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000212	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000256	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000343	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000347	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000358	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000369	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000454	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000455	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000463	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000520	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000668	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000678	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000689	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000692	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000902	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000921	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001156	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001159	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001627	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001629	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001631	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001642	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001680	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001792	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0002007	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0002164	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0002650	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0002751	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0002937	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0003196	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0005280	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0006439	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0009611	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0009882	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0009890	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0010296	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0010297	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0010882	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0011662	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0011800	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0030039	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0030264	ORPHA:97360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000003	ORPHA:97360	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0000410	ORPHA:97360	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0001537	ORPHA:97360	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0006291	ORPHA:97360	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0006335	ORPHA:97360	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0012758	ORPHA:97360	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97360	Robinow syndrome		HP:0040171	ORPHA:97360	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0002573	ORPHA:209964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0002027	ORPHA:209964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0002254	ORPHA:209964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0012450	ORPHA:209964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0500005	ORPHA:209964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0000002	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0000722	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0001903	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0002035	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0002574	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0004325	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0012390	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0012702	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0025085	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0025086	ORPHA:209964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209964	Solitary rectal ulcer syndrome		HP:0012425	ORPHA:209964	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0001012	ORPHA:199276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0001031	ORPHA:199276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0001513	ORPHA:199276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0006773	ORPHA:199276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0009830	ORPHA:199276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0025502	ORPHA:199276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0007596	ORPHA:199276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199276	Familial multiple lipomatosis		HP:0007618	ORPHA:199276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000750	ORPHA:254531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0001252	ORPHA:254531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0001270	ORPHA:254531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0001382	ORPHA:254531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0001511	ORPHA:254531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0001773	ORPHA:254531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0200055	ORPHA:254531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000826	ORPHA:254531	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0001513	ORPHA:254531	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0008897	ORPHA:254531	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0011220	ORPHA:254531	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0011968	ORPHA:254531	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000218	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000322	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000347	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000403	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000445	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000729	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0012760	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0000817	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0001249	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0002650	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0003124	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0004673	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0004904	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0007010	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0008947	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254531	Temple syndrome due to paternal 14q32.2 hypomethylation		HP:0030084	ORPHA:254531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000089	ORPHA:97362	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000076	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000093	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000107	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000822	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001562	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0002009	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0011968	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0012213	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0012622	ORPHA:97362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000028	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000483	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000540	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000639	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0000969	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001254	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001508	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001510	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001518	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001622	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001903	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0001942	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0002153	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0002643	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0002902	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0002907	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0003076	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0004322	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0012758	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0025466	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97362	Renal hypoplasia, bilateral		HP:0100520	ORPHA:97362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000750	ORPHA:263487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001270	ORPHA:263487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0008947	ORPHA:263487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000252	ORPHA:263487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000358	ORPHA:263487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000369	ORPHA:263487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000448	ORPHA:263487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0004322	ORPHA:263487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0010864	ORPHA:263487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000011	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000020	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000028	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000054	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000218	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000278	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000407	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000431	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000470	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000486	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000599	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0000729	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001250	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001256	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001272	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001348	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001433	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001511	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0001562	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0002078	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0002240	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0002342	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0002506	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0002857	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0002910	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0003160	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0006956	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0007366	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0009473	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0011471	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0012444	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0012448	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0012762	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0040019	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0100490	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0100678	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263487	COG5-CDG		HP:0100704	ORPHA:263487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001256	ORPHA:254534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001263	ORPHA:254534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001561	ORPHA:254534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0005257	ORPHA:254534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0006267	ORPHA:254534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0006665	ORPHA:254534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0008872	ORPHA:254534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001252	ORPHA:254534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001520	ORPHA:254534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001540	ORPHA:254534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0002033	ORPHA:254534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0008897	ORPHA:254534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001518	ORPHA:254534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001537	ORPHA:254534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001539	ORPHA:254534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001548	ORPHA:254534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001627	ORPHA:254534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0001629	ORPHA:254534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254534	Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation		HP:0002194	ORPHA:254534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494444	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome		HP:0000408	ORPHA:494444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494444	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome		HP:0001873	ORPHA:494444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494444	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome		HP:0011877	ORPHA:494444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494444	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome		HP:0001875	ORPHA:494444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494444	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome		HP:0001891	ORPHA:494444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494444	DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome		HP:0006285	ORPHA:494444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0000483	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0000512	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0000545	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0000551	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0000639	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0007663	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0007750	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0007894	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178333	Åland Islands eye disease		HP:0030513	ORPHA:178333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0001618	ORPHA:399058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0002015	ORPHA:399058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0009063	ORPHA:399058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0000467	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0001265	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0003325	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0003327	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0003458	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0003557	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0003736	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0009027	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0030225	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0040081	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0100020	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0100299	ORPHA:399058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0001349	ORPHA:399058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0001638	ORPHA:399058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0001288	ORPHA:399058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0002747	ORPHA:399058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0003552	ORPHA:399058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399058	Alpha-B crystallin-related late-onset myopathy		HP:0009073	ORPHA:399058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000253	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000347	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000938	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001263	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001290	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001321	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001344	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001508	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001999	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002058	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002123	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002421	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002650	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0003236	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0003642	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0005781	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0007179	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0011169	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0200134	ORPHA:329178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000218	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000219	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000243	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000294	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000486	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000601	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000648	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0000689	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001561	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0001976	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002002	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002098	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002205	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002240	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002518	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0002910	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0003196	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0003241	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0010851	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0012762	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy		HP:0040288	ORPHA:329178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0001300	ORPHA:97355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002063	ORPHA:97355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002067	ORPHA:97355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0000511	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0000571	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0000726	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0000727	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0000738	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0001278	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0001332	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0001336	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002119	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002120	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002172	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002186	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002193	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002345	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0002360	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0003458	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0005341	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0007045	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0007240	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0010549	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0012332	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0012753	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism		HP:0030902	ORPHA:97355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97355	Caribbean parkinsonism	NOT	HP:0100315	ORPHA:97355	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0000613	ORPHA:209967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0001251	ORPHA:209967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0002017	ORPHA:209967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0002321	ORPHA:209967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0002183	ORPHA:209967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0000640	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0000651	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0001250	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0001272	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0001350	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0002076	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0002301	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0002315	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209967	Episodic ataxia type 6		HP:0007663	ORPHA:209967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001249	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001263	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001347	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001371	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0002460	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0002540	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0002987	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0006380	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0006466	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0007350	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0012453	ORPHA:209951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000154	ORPHA:209951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000158	ORPHA:209951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001257	ORPHA:209951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001344	ORPHA:209951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0002079	ORPHA:209951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0003487	ORPHA:209951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000218	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000322	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000377	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000574	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000664	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0000666	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001250	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0001583	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0002015	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0002166	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0002378	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0003273	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0003306	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0005830	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0005997	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0011448	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209951	Autosomal spastic paraplegia type 18		HP:0100712	ORPHA:209951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199267	Infantile digital fibromatosis		HP:0200036	ORPHA:199267	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199267	Infantile digital fibromatosis		HP:0000962	ORPHA:199267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199267	Infantile digital fibromatosis		HP:0001036	ORPHA:199267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199267	Infantile digital fibromatosis		HP:0025092	ORPHA:199267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199267	Infantile digital fibromatosis		HP:0012531	ORPHA:199267	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0001089	ORPHA:263479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0025341	ORPHA:263479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0031701	ORPHA:263479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0100832	ORPHA:263479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0000518	ORPHA:263479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0000622	ORPHA:263479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0001100	ORPHA:263479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0034820	ORPHA:263479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0034821	ORPHA:263479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0000501	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0000613	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0001085	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0007663	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0007777	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0007906	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0025337	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0030534	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0200026	ORPHA:263479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0000543	ORPHA:263479	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0009916	ORPHA:263479	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0011958	ORPHA:263479	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0030554	ORPHA:263479	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis		HP:0100014	ORPHA:263479	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263479	Fuchs heterochromic iridocyclitis	NOT	HP:0011484	ORPHA:263479	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000992	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002013	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002015	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002018	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002024	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002315	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0004326	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0004395	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0004396	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0005263	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0007400	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0008066	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0010280	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0012378	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0012531	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0031258	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0100543	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0100753	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0100825	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0100497	ORPHA:97352	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000158	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000206	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000716	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000726	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000738	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000958	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000962	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000988	ORPHA:97352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000613	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000712	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0000739	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0001324	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002014	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002019	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0002360	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0003401	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0007141	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0025300	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0031987	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0032448	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0033505	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0100653	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97352	Pellagra		HP:0200037	ORPHA:97352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0500006	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0000509	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0000962	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001369	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001386	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001387	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001597	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002014	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002754	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002829	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0008391	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0011107	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0100543	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0100686	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0100773	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0200039	ORPHA:29207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0000988	ORPHA:29207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001101	ORPHA:29207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002027	ORPHA:29207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002037	ORPHA:29207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002103	ORPHA:29207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0003419	ORPHA:29207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0000010	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0000554	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0000613	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001659	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001701	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001824	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0001945	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002093	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0002206	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0003565	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0011227	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0012219	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0012317	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29207	Reactive arthritis		HP:0034438	ORPHA:29207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0000750	ORPHA:254525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001252	ORPHA:254525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001270	ORPHA:254525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001773	ORPHA:254525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0008897	ORPHA:254525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0200055	ORPHA:254525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001319	ORPHA:254525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001511	ORPHA:254525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0011220	ORPHA:254525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0000119	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0000347	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0000358	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0000826	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001249	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001513	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0001627	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0002714	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0004482	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0007010	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0008872	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0030084	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254525	Temple syndrome due to paternal 14q32.2 microdeletion		HP:0031878	ORPHA:254525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001263	ORPHA:254528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001561	ORPHA:254528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0005257	ORPHA:254528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0006665	ORPHA:254528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0011968	ORPHA:254528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000023	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001371	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001382	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001537	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001540	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0002878	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0006267	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0008897	ORPHA:254528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000126	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000158	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000194	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000278	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000286	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000337	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000341	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000463	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000565	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000767	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000884	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0000954	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001239	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001252	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001539	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001601	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001845	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0002263	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0005280	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0005989	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0010511	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0012385	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0012785	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0045025	ORPHA:254528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254528	Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion		HP:0001511	ORPHA:254528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0001270	ORPHA:314918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0001328	ORPHA:314918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0002465	ORPHA:314918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0011342	ORPHA:314918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0012379	ORPHA:314918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0000256	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0000510	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0000750	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0001250	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0001252	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0001347	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0002421	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0002493	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0003487	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0012751	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314918	Mild Canavan disease		HP:0040196	ORPHA:314918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0012379	ORPHA:171706	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0002925	ORPHA:171706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0031506	ORPHA:171706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0032210	ORPHA:171706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0000508	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0000736	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0001249	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0001510	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0001513	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0002750	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0003162	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0003391	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0004322	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0008994	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0009053	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0012548	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0031903	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171706	Short stature-delayed bone age due to thyroid hormone metabolism deficiency		HP:0040214	ORPHA:171706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome		HP:0001274	ORPHA:171703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome		HP:0001321	ORPHA:171703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome		HP:0002098	ORPHA:171703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome		HP:0002119	ORPHA:171703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome		HP:0002126	ORPHA:171703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome		HP:0002719	ORPHA:171703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome		HP:0011451	ORPHA:171703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0000572	ORPHA:209959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0200026	ORPHA:209959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0500081	ORPHA:209959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0000491	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0000613	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0000615	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0000622	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0007773	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0011488	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0012122	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0012123	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0025337	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0030953	ORPHA:209959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0004327	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0007906	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0007917	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0008030	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0011484	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0011505	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0011531	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0011886	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0012040	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0012121	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0025341	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0025561	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0030485	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0030486	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0031615	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0031618	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209959	Phacoanaphylactic uveitis		HP:0040049	ORPHA:209959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0000256	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001252	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001263	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001270	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001344	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002421	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002540	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0004302	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0025053	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0025405	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0034649	ORPHA:314911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0000648	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0000737	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001250	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001254	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001347	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001387	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001612	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002013	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002020	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002033	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002069	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002360	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0003487	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0011968	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0012762	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0200136	ORPHA:314911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0000618	ORPHA:314911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001257	ORPHA:314911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0001355	ORPHA:314911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0040288	ORPHA:314911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0002200	ORPHA:314911	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0011471	ORPHA:314911	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314911	Severe Canavan disease		HP:0025013	ORPHA:314911	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002322	ORPHA:97349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0001945	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002067	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002329	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002396	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002465	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0003324	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0003487	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0004305	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0007256	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0010553	ORPHA:97349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0000194	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0000496	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0000514	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0000716	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0001250	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0001260	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0001488	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002013	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002015	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002063	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002304	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002315	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002374	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002381	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002795	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0002808	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0003401	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0005329	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0006801	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0000718	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0008765	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0011446	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0012735	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0025331	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0025456	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0030188	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0040082	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0045007	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0100595	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97349	Postencephalitic parkinsonism		HP:0200149	ORPHA:97349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0000591	ORPHA:209956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0002922	ORPHA:209956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0004328	ORPHA:209956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0007663	ORPHA:209956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0012231	ORPHA:209956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0025339	ORPHA:209956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0030823	ORPHA:209956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0031526	ORPHA:209956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0000568	ORPHA:209956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0000622	ORPHA:209956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0001123	ORPHA:209956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0008052	ORPHA:209956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome		HP:0012508	ORPHA:209956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209956	Idiopathic uveal effusion syndrome	NOT	HP:0012632	ORPHA:209956	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:211	Familial cylindromatosis		HP:0001482	ORPHA:211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:211	Familial cylindromatosis		HP:0100585	ORPHA:211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000093	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000112	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000124	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000613	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000821	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000823	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001324	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001508	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001944	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001959	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001994	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002013	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002148	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002900	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0003198	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0003355	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0004322	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0007957	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0009806	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0012378	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0100651	ORPHA:213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000083	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000121	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000135	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000488	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000585	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000787	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001510	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001744	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001942	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002240	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002748	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002749	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002901	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0003076	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0003109	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0003155	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0003458	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0011968	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0012072	ORPHA:213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000027	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0000505	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001252	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001256	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001288	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001409	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001738	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001945	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0001952	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002019	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002024	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002381	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0002902	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0003234	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0006824	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:213	Cystinosis		HP:0012093	ORPHA:213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000505	ORPHA:98673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000648	ORPHA:98673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000407	ORPHA:98673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000551	ORPHA:98673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000602	ORPHA:98673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0007141	ORPHA:98673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0012511	ORPHA:98673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0025514	ORPHA:98673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0030515	ORPHA:98673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000508	ORPHA:98673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000603	ORPHA:98673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001251	ORPHA:98673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001288	ORPHA:98673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0003198	ORPHA:98673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000135	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000518	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000639	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000726	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000738	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000819	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0000821	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001250	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001257	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001258	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001263	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001269	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001272	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001284	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001761	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0001972	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0002015	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0002076	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0002135	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0002518	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0003202	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0003326	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0003691	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0007366	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0007371	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0009921	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0011968	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0012378	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0030319	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98673	Autosomal dominant optic atrophy, classic form		HP:0100543	ORPHA:98673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0003153	ORPHA:212	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0001249	ORPHA:212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0001250	ORPHA:212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0003286	ORPHA:212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0000787	ORPHA:212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0001337	ORPHA:212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0001762	ORPHA:212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:212	Cystathioninuria		HP:0000377	ORPHA:212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0007663	ORPHA:97341	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0011506	ORPHA:97341	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0001103	ORPHA:97341	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0000646	ORPHA:97341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0007750	ORPHA:97341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0007814	ORPHA:97341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0010822	ORPHA:97341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97341	Persistent placoid maculopathy		HP:0012508	ORPHA:97341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199251	Ledderhose disease		HP:0001482	ORPHA:199251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199251	Ledderhose disease		HP:0002829	ORPHA:199251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199251	Ledderhose disease		HP:0003401	ORPHA:199251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199251	Ledderhose disease		HP:0009830	ORPHA:199251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199251	Ledderhose disease		HP:0100679	ORPHA:199251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0001891	ORPHA:209981	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0004840	ORPHA:209981	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0025066	ORPHA:209981	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0012464	ORPHA:209981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0031877	ORPHA:209981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0040303	ORPHA:209981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0001017	ORPHA:209981	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0030318	ORPHA:209981	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0001596	ORPHA:209981	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209981	IRIDA syndrome		HP:0001598	ORPHA:209981	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0000316	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0001156	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0001371	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0001552	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002515	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002650	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002829	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002857	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002945	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002967	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0003037	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0003312	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0003521	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0008905	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0009811	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0010582	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0010585	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0045075	ORPHA:263463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0000337	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0000343	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0000684	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0001270	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002553	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0002751	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0010049	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263463	CHST3-related skeletal dysplasia		HP:0030680	ORPHA:263463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0000826	ORPHA:254516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0001270	ORPHA:254516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0001518	ORPHA:254516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0001773	ORPHA:254516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0008897	ORPHA:254516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0008947	ORPHA:254516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0200055	ORPHA:254516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0000750	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0001256	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0001513	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0001622	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0004322	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0004482	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0008872	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0011968	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0040288	ORPHA:254516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0000028	ORPHA:254516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0002591	ORPHA:254516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0002650	ORPHA:254516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0005978	ORPHA:254516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0000193	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0000238	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0000307	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0000824	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0001988	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0002007	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0004209	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254516	Temple syndrome		HP:0007429	ORPHA:254516	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000289	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000293	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000347	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000463	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000465	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000470	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001249	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001263	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001376	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001561	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001591	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002015	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002033	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002421	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0004887	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0005257	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0005280	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0006267	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0006665	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0011968	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0025336	ORPHA:254519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000205	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000581	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001520	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001539	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001540	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001601	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001622	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002007	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002019	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002673	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002751	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0011335	ORPHA:254519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0000023	ORPHA:254519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001548	ORPHA:254519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001626	ORPHA:254519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0002884	ORPHA:254519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0008551	ORPHA:254519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0008897	ORPHA:254519	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254519	Kagami-Ogata syndrome		HP:0001250	ORPHA:254519	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0000016	ORPHA:254509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0000217	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0000508	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0001278	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0001324	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0002015	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0002019	ORPHA:254509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0002094	ORPHA:254509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0006597	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0006824	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0011499	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0012378	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254509	Iatrogenic botulism		HP:0100021	ORPHA:254509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000253	ORPHA:481152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001249	ORPHA:481152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001344	ORPHA:481152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001508	ORPHA:481152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002540	ORPHA:481152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0011344	ORPHA:481152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0011968	ORPHA:481152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000327	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000369	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000411	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000414	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001250	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001252	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001257	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001999	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002013	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002079	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002376	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0003202	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0003429	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0007258	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0030890	ORPHA:481152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000218	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000233	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000316	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000319	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000325	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000341	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000343	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000365	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000396	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000400	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000463	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000494	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000565	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000582	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000639	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000718	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000737	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000768	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0000924	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001166	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001251	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001274	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001347	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001371	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001382	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002069	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002283	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0001288	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002365	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002465	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002509	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0002827	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0005072	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0005659	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0006460	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0010055	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0011166	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0011229	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0011304	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481152	PYCR2-related microcephaly-progressive leukoencephalopathy		HP:0100704	ORPHA:481152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0009810	ORPHA:97336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0040188	ORPHA:97336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0001377	ORPHA:97336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0001386	ORPHA:97336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0002996	ORPHA:97336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0031095	ORPHA:97336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0030835	ORPHA:97336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0001871	ORPHA:97336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0003945	ORPHA:97336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0025259	ORPHA:97336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97336	Panner disease		HP:0030865	ORPHA:97336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000189	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000238	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000248	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000262	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000316	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000327	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000348	ORPHA:207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000365	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000405	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000444	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000453	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000486	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000508	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000509	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000520	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000612	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000646	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000648	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000929	ORPHA:207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000956	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0000995	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0001053	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0001321	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0001999	ORPHA:207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0002007	ORPHA:207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0002093	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0002308	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0002315	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0002516	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0005107	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0011324	ORPHA:207	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0011386	ORPHA:207	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:207	Crouzon syndrome		HP:0011800	ORPHA:207	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0030839	ORPHA:97335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0001288	ORPHA:97335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0003045	ORPHA:97335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0003066	ORPHA:97335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0006456	ORPHA:97335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0009046	ORPHA:97335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0002362	ORPHA:97335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97335	Osgood-Schlatter disease		HP:0030866	ORPHA:97335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0000726	ORPHA:204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002529	ORPHA:204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0006790	ORPHA:204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0012672	ORPHA:204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0030890	ORPHA:204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0000708	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0001251	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0001289	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0001336	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002059	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002100	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002171	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002354	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002367	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002446	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002521	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002719	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002922	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0004887	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0100543	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0100806	ORPHA:204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0000505	ORPHA:204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0001257	ORPHA:204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002071	ORPHA:204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0002493	ORPHA:204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0003487	ORPHA:204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0006801	ORPHA:204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:204	Sporadic Creutzfeldt-Jakob disease		HP:0007256	ORPHA:204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0000238	ORPHA:137817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0000360	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0000365	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0000478	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0000504	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0000763	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0000970	ORPHA:137817	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0001265	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0001287	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0001324	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0002076	ORPHA:137817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0002829	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0002839	ORPHA:137817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0003401	ORPHA:137817	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137817	Arachnoiditis		HP:0012378	ORPHA:137817	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000238	ORPHA:97339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001977	ORPHA:97339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0004947	ORPHA:97339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0008629	ORPHA:97339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0030724	ORPHA:97339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000256	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000501	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000504	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000520	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000572	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000932	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001085	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001268	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001297	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001317	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001324	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001342	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002017	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002138	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002170	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002196	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002315	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002311	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002463	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002516	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0003474	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0007906	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0011342	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0011695	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0012375	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0031157	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0100309	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:3000043	ORPHA:97339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000651	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000726	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0000741	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001250	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001251	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001269	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0001300	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002167	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002181	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002273	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0002617	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0006824	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0007333	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0011343	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97339	Dural sinus malformation		HP:0030766	ORPHA:97339	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0000952	ORPHA:205	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0003265	ORPHA:205	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0008282	ORPHA:205	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0001252	ORPHA:205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0002033	ORPHA:205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0000365	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0000597	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0000989	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0001250	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0001254	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0001259	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0001343	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0001433	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0002179	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0002321	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0002329	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0002354	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0002383	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0006297	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0006958	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0025430	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:205	Crigler-Najjar syndrome		HP:0100543	ORPHA:205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97337	Sinding-Larsen-Johansson disease		HP:0030839	ORPHA:97337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97337	Sinding-Larsen-Johansson disease		HP:0001386	ORPHA:97337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97337	Sinding-Larsen-Johansson disease		HP:0010501	ORPHA:97337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97337	Sinding-Larsen-Johansson disease		HP:0040188	ORPHA:97337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97337	Sinding-Larsen-Johansson disease		HP:0002661	ORPHA:97337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0001274	ORPHA:200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0000736	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0000750	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0001252	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0001328	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0002015	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0002342	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0002311	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0002463	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0010522	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0010864	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:0031843	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:200	Isolated corpus callosum agenesis		HP:6000915	ORPHA:200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000036	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000077	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000130	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000158	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000218	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000221	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000256	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000365	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000518	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000545	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000717	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000767	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000771	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000820	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000853	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000982	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0000995	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001048	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001053	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001156	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001249	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001250	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001251	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001263	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001317	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001482	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0001508	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0002516	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0002650	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0002664	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0002808	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0002858	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0002861	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0003002	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0004322	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0004390	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0005374	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0005584	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0005595	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0006731	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0007565	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0008069	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0008675	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0009720	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0010614	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0012032	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0012062	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0012114	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0012733	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0012740	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0100006	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0100031	ORPHA:201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0100543	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0100579	ORPHA:201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0100780	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0200034	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:201	Cowden syndrome		HP:0200063	ORPHA:201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0011744	ORPHA:199244	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0011749	ORPHA:199244	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0003118	ORPHA:199244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0008291	ORPHA:199244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0012030	ORPHA:199244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0000505	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0000822	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0001065	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0002900	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0005978	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0007340	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0007440	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0007924	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0030521	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0030591	ORPHA:199244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0000830	ORPHA:199244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0002516	ORPHA:199244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0007807	ORPHA:199244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0009050	ORPHA:199244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0012246	ORPHA:199244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0000870	ORPHA:199244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0000873	ORPHA:199244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0002170	ORPHA:199244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0010788	ORPHA:199244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0011763	ORPHA:199244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0200026	ORPHA:199244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199244	Nelson syndrome		HP:0430022	ORPHA:199244	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97332	Kienbock disease		HP:0001376	ORPHA:97332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97332	Kienbock disease		HP:0002653	ORPHA:97332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97332	Kienbock disease		HP:0002758	ORPHA:97332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97332	Kienbock disease		HP:0002829	ORPHA:97332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97332	Kienbock disease		HP:0003019	ORPHA:97332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97332	Kienbock disease		HP:0010885	ORPHA:97332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97332	Kienbock disease		HP:0010886	ORPHA:97332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0000825	ORPHA:263458	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0001943	ORPHA:263458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0001988	ORPHA:263458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0008283	ORPHA:263458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0030794	ORPHA:263458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0001250	ORPHA:263458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0012378	ORPHA:263458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0000855	ORPHA:263458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263458	Hyperinsulinism due to INSR deficiency		HP:0001259	ORPHA:263458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0000763	ORPHA:97330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0000772	ORPHA:97330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0000969	ORPHA:97330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0001324	ORPHA:97330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0002619	ORPHA:97330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0002829	ORPHA:97330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0003326	ORPHA:97330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0003394	ORPHA:97330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0003401	ORPHA:97330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0003457	ORPHA:97330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97330	Thoracic outlet syndrome		HP:0004936	ORPHA:97330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0000093	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0000713	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0000825	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0000842	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0000975	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0000980	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001249	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001250	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001254	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001259	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001319	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001337	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0002240	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001520	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001649	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001985	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001994	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0001998	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0002013	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0002014	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0002329	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0002344	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0002910	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0003076	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0003155	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0003162	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0004324	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0004359	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0004510	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0004912	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0005979	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0006568	ORPHA:263455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263455	Congenital hyperinsulinism due to HNF4A deficiency		HP:0012378	ORPHA:263455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0002716	ORPHA:199241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0005954	ORPHA:199241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0025104	ORPHA:199241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0025179	ORPHA:199241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0030879	ORPHA:199241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0045051	ORPHA:199241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0000961	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0001708	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0002094	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0002105	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0002875	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0004890	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0010741	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0012151	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0012418	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0025180	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0025420	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0030968	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0100721	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0100759	ORPHA:199241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0002202	ORPHA:199241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0100598	ORPHA:199241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis		HP:0001698	ORPHA:199241	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis	NOT	HP:0003493	ORPHA:199241	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:199241	Pulmonary capillary hemangiomatosis	NOT	HP:0032230	ORPHA:199241	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0001260	ORPHA:209970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0001324	ORPHA:209970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0002131	ORPHA:209970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0002321	ORPHA:209970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0000639	ORPHA:209970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0000360	ORPHA:209970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0000651	ORPHA:209970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0002076	ORPHA:209970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0002411	ORPHA:209970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0002487	ORPHA:209970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209970	Episodic ataxia type 7		HP:0100543	ORPHA:209970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0002090	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0002094	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0002098	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0002113	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0002789	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0002878	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0011112	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0011227	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0012418	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0030783	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0032094	ORPHA:178320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0000969	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0001735	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0001945	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0002105	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0006530	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0011118	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0025420	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0030955	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0031273	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178320	Acute lung injury		HP:0100806	ORPHA:178320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0000016	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0000217	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0000508	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0000651	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0001324	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0002014	ORPHA:254504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0002017	ORPHA:254504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0002019	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0002094	ORPHA:254504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0003470	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0006824	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0011499	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254504	Inhalational botulism		HP:0012378	ORPHA:254504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000256	ORPHA:457485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001249	ORPHA:457485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001355	ORPHA:457485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001250	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001263	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001328	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001520	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001999	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002007	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002119	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002167	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002197	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002212	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0007359	ORPHA:457485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000028	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000154	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000194	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000316	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000343	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000486	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000729	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000752	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000957	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001028	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001053	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001252	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001273	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001288	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001538	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001540	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001763	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002099	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002126	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0004789	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0005257	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0011220	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0025104	ORPHA:457485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000047	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000331	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0000494	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0001998	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0002720	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0005266	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0005280	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457485	Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome		HP:0012393	ORPHA:457485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001156	ORPHA:65759	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001770	ORPHA:65759	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0006101	ORPHA:65759	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000028	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000098	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000256	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000263	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000275	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000286	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000316	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000929	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001159	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001249	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001357	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001363	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001513	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0003241	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0004209	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0004279	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0005487	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0010442	ORPHA:65759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000262	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000445	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000457	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000481	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0000486	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001162	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001841	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0002676	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0002857	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0011304	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0012243	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0030680	ORPHA:65759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001537	ORPHA:65759	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001643	ORPHA:65759	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001748	ORPHA:65759	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0001762	ORPHA:65759	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0002751	ORPHA:65759	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0010044	ORPHA:65759	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65759	Carpenter syndrome		HP:0100490	ORPHA:65759	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0009934	ORPHA:141091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0010938	ORPHA:141091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0010939	ORPHA:141091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0000202	ORPHA:141091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0000316	ORPHA:141091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0002056	ORPHA:141091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0002693	ORPHA:141091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0006956	ORPHA:141091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141091	Polyrrhinia		HP:0010951	ORPHA:141091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0012382	ORPHA:99103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0001962	ORPHA:99103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0002875	ORPHA:99103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0003546	ORPHA:99103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0012378	ORPHA:99103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0030718	ORPHA:99103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0031664	ORPHA:99103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0001633	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0001635	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0001653	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0002092	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0002094	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0004749	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0004755	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0005110	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0005115	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0005133	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0005162	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0005180	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0005957	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0010741	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0011675	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0011705	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0011710	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0012250	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0012764	ORPHA:99103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0000961	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0001279	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0001297	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0001708	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0002090	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0002326	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0002718	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0005317	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99103	Atrial septal defect, ostium secundum type		HP:0006536	ORPHA:99103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000248	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000256	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000316	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000337	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000348	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000365	ORPHA:178377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000505	ORPHA:178377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0000648	ORPHA:178377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0001363	ORPHA:178377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0002315	ORPHA:178377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0002516	ORPHA:178377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0002684	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0010628	ORPHA:178377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0011001	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0011342	ORPHA:178377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178377	Osteosclerosis-developmental delay-craniosynostosis syndrome		HP:0012802	ORPHA:178377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0001249	ORPHA:137831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0001263	ORPHA:137831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0001321	ORPHA:137831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0000486	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0000490	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0000729	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0012760	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0000817	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0001251	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0001252	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0001290	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0001999	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002119	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002123	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002167	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002342	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002384	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002465	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002951	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0010864	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0400000	ORPHA:137831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0000303	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0000431	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0000448	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002080	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002172	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002280	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0002340	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0006817	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0006913	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0006951	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0007018	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome		HP:0007112	ORPHA:137831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000154	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000280	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000316	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000322	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000431	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000490	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0001061	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0001072	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0001156	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0001634	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0002797	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0005280	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0010885	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0012471	ORPHA:137834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000212	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000303	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000337	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000348	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000411	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000494	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000684	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0001387	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0002650	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0002808	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0002816	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0004209	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0004568	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0005916	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0006480	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0100490	ORPHA:137834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000023	ORPHA:137834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0000771	ORPHA:137834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137834	Frank-Ter Haar syndrome		HP:0001537	ORPHA:137834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000245	ORPHA:141099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0012806	ORPHA:141099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000625	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0002011	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0002119	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0009932	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0011821	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0012372	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0032039	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0430023	ORPHA:141099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000202	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000218	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000256	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000316	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000337	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000343	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000534	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000567	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000579	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000609	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000612	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000614	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0001273	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0001360	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0003241	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0007957	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0009117	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0040296	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0430005	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:3000030	ORPHA:141099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000122	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000286	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000453	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000482	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000486	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000508	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000518	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000520	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000528	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000568	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0000588	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0001144	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0001629	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0001643	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0005580	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0007946	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0009914	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0012300	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141099	Proboscis lateralis		HP:0012738	ORPHA:141099	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0000083	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0000093	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0000100	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0000822	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0001342	ORPHA:84090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0001966	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0002907	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0003073	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0010741	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84090	Fibronectin glomerulopathy		HP:0100820	ORPHA:84090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141096	Supernumerary nostril		HP:0009934	ORPHA:141096	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:141096	Supernumerary nostril		HP:0000271	ORPHA:141096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141096	Supernumerary nostril		HP:0002006	ORPHA:141096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141096	Supernumerary nostril		HP:0000453	ORPHA:141096	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141096	Supernumerary nostril		HP:0000482	ORPHA:141096	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141096	Supernumerary nostril		HP:0000519	ORPHA:141096	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:141096	Supernumerary nostril		HP:3000040	ORPHA:141096	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0009830	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0011951	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0011968	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0030680	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0031282	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0031423	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000062	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000126	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000218	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000413	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000486	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000518	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000878	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001305	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001894	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002126	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002139	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002937	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0003298	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0004626	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0006934	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0008110	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0008221	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0010497	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0011326	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0011409	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0012725	ORPHA:79500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000212	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000343	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000431	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000463	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001167	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001231	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001263	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001780	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001817	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002353	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0008388	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0012810	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0100797	ORPHA:79500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000179	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000194	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000219	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000280	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000286	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000294	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000316	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000369	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000414	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000474	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001265	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001561	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002033	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002069	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002384	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002714	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0004209	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0008947	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0009237	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0009882	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0010347	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0012402	ORPHA:79500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000079	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000121	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000164	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000175	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000187	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000189	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000200	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000248	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000252	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000269	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000455	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000545	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000648	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000675	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000687	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000696	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000729	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0000851	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001199	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001336	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001488	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0001719	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002007	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002020	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0002098	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0004442	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79500	DOORS syndrome		HP:0005306	ORPHA:79500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0000972	ORPHA:79501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0000982	ORPHA:79501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0011124	ORPHA:79501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0045059	ORPHA:79501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0025092	ORPHA:79501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0025114	ORPHA:79501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0040162	ORPHA:79501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0002861	ORPHA:79501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0003002	ORPHA:79501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0012500	ORPHA:79501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0012531	ORPHA:79501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0100751	ORPHA:79501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0002671	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0002860	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0005584	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0006725	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0008404	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0010622	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0012125	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0012126	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0012189	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0030692	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0040274	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0040276	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79501	Punctate palmoplantar keratoderma type 1		HP:0100526	ORPHA:79501	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0002342	ORPHA:96061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000076	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000126	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000268	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000276	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000316	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000347	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000377	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000400	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000411	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000445	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000455	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000463	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000486	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000490	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000772	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000774	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0001376	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0001869	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0002007	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0002650	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0003275	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0003422	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0006191	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0006443	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0007957	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0009738	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0100490	ORPHA:96061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000028	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000098	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000175	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000218	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000365	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0000470	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0001010	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0001053	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0001274	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0002804	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0004209	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0004322	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0008734	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96061	Mosaic trisomy 8 syndrome		HP:0030680	ORPHA:96061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3294	Extensor tendons of finger anomalies		HP:0000991	ORPHA:3294	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3294	Extensor tendons of finger anomalies		HP:0001012	ORPHA:3294	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3294	Extensor tendons of finger anomalies		HP:0100490	ORPHA:3294	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3294	Extensor tendons of finger anomalies		HP:0000939	ORPHA:3294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3294	Extensor tendons of finger anomalies		HP:0001376	ORPHA:3294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3294	Extensor tendons of finger anomalies		HP:0003202	ORPHA:3294	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263432	Nevus of Ito		HP:0003764	ORPHA:263432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263432	Nevus of Ito		HP:0012056	ORPHA:263432	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:263432	Nevus of Ito	NOT	HP:0025534	ORPHA:263432	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0003125	ORPHA:35909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0003225	ORPHA:35909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0003645	ORPHA:35909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0008151	ORPHA:35909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0000225	ORPHA:35909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0000421	ORPHA:35909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0000978	ORPHA:35909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0006298	ORPHA:35909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0011889	ORPHA:35909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0030137	ORPHA:35909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0000132	ORPHA:35909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0000790	ORPHA:35909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0002170	ORPHA:35909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0002239	ORPHA:35909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0004846	ORPHA:35909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0005261	ORPHA:35909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0002149	ORPHA:35909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35909	Combined deficiency of factor V and factor VIII		HP:0003077	ORPHA:35909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84085	Hinman syndrome		HP:0000010	ORPHA:84085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84085	Hinman syndrome		HP:0000076	ORPHA:84085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84085	Hinman syndrome		HP:0000083	ORPHA:84085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84085	Hinman syndrome		HP:0000126	ORPHA:84085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84085	Hinman syndrome		HP:0000805	ORPHA:84085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84085	Hinman syndrome		HP:0002019	ORPHA:84085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84085	Hinman syndrome		HP:0002607	ORPHA:84085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0000089	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0000108	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0000822	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001395	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001396	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001409	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001433	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001959	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0002910	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0003155	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0003573	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0004719	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0005565	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0006563	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0006571	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0012591	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0012622	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0020132	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0032581	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0032622	ORPHA:84081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0000713	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0000718	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001394	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001541	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0001903	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0002040	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0002500	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0002506	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0002612	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0003774	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0007018	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0012163	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0012585	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84081	Senior-Boichis syndrome		HP:0031589	ORPHA:84081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0008138	ORPHA:178382	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0001436	ORPHA:178382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0001771	ORPHA:178382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0001838	ORPHA:178382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0008081	ORPHA:178382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0030311	ORPHA:178382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0000707	ORPHA:178382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0001763	ORPHA:178382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0005684	ORPHA:178382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0025238	ORPHA:178382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0002475	ORPHA:178382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0030268	ORPHA:178382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178382	Congenital vertical talus		HP:0030840	ORPHA:178382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209919	Idiopathic copper-associated cirrhosis		HP:0001394	ORPHA:209919	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:209919	Idiopathic copper-associated cirrhosis		HP:0025321	ORPHA:209919	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:209919	Idiopathic copper-associated cirrhosis		HP:0001397	ORPHA:209919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209919	Idiopathic copper-associated cirrhosis		HP:0010839	ORPHA:209919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209919	Idiopathic copper-associated cirrhosis		HP:0032254	ORPHA:209919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209919	Idiopathic copper-associated cirrhosis	NOT	HP:0010837	ORPHA:209919	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0000211	ORPHA:3299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002015	ORPHA:3299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002179	ORPHA:3299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0003552	ORPHA:3299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0040212	ORPHA:3299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0001276	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0001649	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0001945	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002063	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0005363	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0011355	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0011964	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0025258	ORPHA:3299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0000822	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0001259	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0001337	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0001662	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002027	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002098	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002501	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002607	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0002789	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0003236	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0003345	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0003639	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0005341	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0006824	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0012332	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0025145	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3299	Tetanus		HP:0025425	ORPHA:3299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0000579	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0000620	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0001742	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0009926	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0012763	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0030215	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0030829	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:3000066	ORPHA:141083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0000646	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0001945	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0002033	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0002719	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0004411	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0004885	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0007651	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0007717	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0010307	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0025337	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0025612	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0030752	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0030864	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0045025	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0100539	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0100658	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141083	Nasolacrimal duct cyst		HP:0200026	ORPHA:141083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0000511	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0001260	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0001310	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0001347	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002066	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002075	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002080	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002136	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002167	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002168	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002313	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0002317	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0004302	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423275	Spinocerebellar ataxia type 40		HP:0006879	ORPHA:423275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183707	Infantile LAD-like disease due to RAC2 deficiency		HP:0001058	ORPHA:183707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183707	Infantile LAD-like disease due to RAC2 deficiency		HP:0001974	ORPHA:183707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183707	Infantile LAD-like disease due to RAC2 deficiency		HP:0002721	ORPHA:183707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183707	Infantile LAD-like disease due to RAC2 deficiency		HP:0011990	ORPHA:183707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0008163	ORPHA:199299	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0011735	ORPHA:199299	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0011748	ORPHA:199299	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001254	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001324	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001508	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001824	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002014	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002017	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002019	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002027	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002039	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002615	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002920	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002960	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0012378	ORPHA:199299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0000872	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001897	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001972	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002149	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002902	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0008209	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0011134	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0100647	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0100651	ORPHA:199299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0000829	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0000958	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001045	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001250	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001278	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001880	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0001943	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002321	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002608	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002829	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0003072	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0006462	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0012115	ORPHA:199299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0002893	ORPHA:199299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency		HP:0100806	ORPHA:199299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199299	Late-onset isolated ACTH deficiency	NOT	HP:0002153	ORPHA:199299	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000100	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000164	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000217	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000246	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000327	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000463	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000958	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000962	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000963	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000964	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0000966	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0001097	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0001508	ORPHA:238468	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0001597	ORPHA:238468	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0001999	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0002007	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0002217	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0004298	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0006482	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0007400	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0009804	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0009886	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0010978	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0011358	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0011362	ORPHA:238468	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0012471	ORPHA:238468	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0012735	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0100533	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0100543	ORPHA:238468	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0100783	ORPHA:238468	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238468	Hypohidrotic ectodermal dysplasia		HP:0100840	ORPHA:238468	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0001649	ORPHA:3282	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0031593	ORPHA:3282	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:6001086	ORPHA:3282	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:6001087	ORPHA:3282	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0004749	ORPHA:3282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0005110	ORPHA:3282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0034376	ORPHA:3282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:6000264	ORPHA:3282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0001629	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0001631	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0001639	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0001642	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0002094	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0002615	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0002789	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0004758	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0005162	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0008872	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0011717	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:4000141	ORPHA:3282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0000028	ORPHA:3282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0000821	ORPHA:3282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0001254	ORPHA:3282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0001279	ORPHA:3282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3282	Multifocal atrial tachycardia		HP:0006671	ORPHA:3282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3283	His bundle tachycardia		HP:0001638	ORPHA:3283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3283	His bundle tachycardia		HP:0011675	ORPHA:3283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3283	His bundle tachycardia		HP:0011716	ORPHA:3283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3283	His bundle tachycardia		HP:0100544	ORPHA:3283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0001998	ORPHA:199296	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0008163	ORPHA:199296	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0011735	ORPHA:199296	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0000835	ORPHA:199296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0002615	ORPHA:199296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0002902	ORPHA:199296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0012378	ORPHA:199296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0002173	ORPHA:199296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0006579	ORPHA:199296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency		HP:0012115	ORPHA:199296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199296	Congenital isolated ACTH deficiency	NOT	HP:0002153	ORPHA:199296	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002273	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002376	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0003487	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0006999	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0007374	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0007811	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0008947	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0012758	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001276	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001336	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002020	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002063	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002359	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002396	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002446	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002505	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0003484	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0006799	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0007340	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0007688	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0012697	ORPHA:225154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0000648	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0000750	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001251	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001256	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001257	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001260	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001266	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001285	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001288	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001332	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001347	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0001508	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002015	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002066	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225154	Familial infantile bilateral striatal necrosis		HP:0002167	ORPHA:225154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0000464	ORPHA:494424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0000707	ORPHA:494424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0000822	ORPHA:494424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0001297	ORPHA:494424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002621	ORPHA:494424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0031910	ORPHA:494424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0000819	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0001269	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0001609	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0001727	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0001977	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002138	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002381	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002633	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002634	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002637	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0003484	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0003549	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0005160	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0006824	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0012089	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0012531	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0031690	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0032169	ORPHA:494424	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002721	ORPHA:494424	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0002960	ORPHA:494424	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0005313	ORPHA:494424	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:494424	Extracranial carotid artery aneurysm		HP:0032271	ORPHA:494424	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0000988	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0001392	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0001903	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0002015	ORPHA:44890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0002017	ORPHA:44890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0002019	ORPHA:44890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0002239	ORPHA:44890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0005214	ORPHA:44890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0006753	ORPHA:44890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0007378	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0007400	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0012378	ORPHA:44890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0100242	ORPHA:44890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0100273	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0100723	ORPHA:44890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0100743	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0100751	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:44890	Gastrointestinal stromal tumor		HP:0100833	ORPHA:44890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0000776	ORPHA:171719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0001166	ORPHA:171719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0001371	ORPHA:171719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0001376	ORPHA:171719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0001582	ORPHA:171719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0001654	ORPHA:171719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0002097	ORPHA:171719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171719	Cutis laxa-Marfanoid syndrome		HP:0002827	ORPHA:171719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0002643	ORPHA:217563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0002789	ORPHA:217563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0006517	ORPHA:217563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0006530	ORPHA:217563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0002092	ORPHA:217563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0002113	ORPHA:217563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0031457	ORPHA:217563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0001667	ORPHA:217563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0004876	ORPHA:217563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0006515	ORPHA:217563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217563	Neonatal acute respiratory distress syndrome		HP:0006528	ORPHA:217563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0004756	ORPHA:3286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0001695	ORPHA:3286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0001962	ORPHA:3286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0002321	ORPHA:3286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0004755	ORPHA:3286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0005110	ORPHA:3286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0031677	ORPHA:3286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0001279	ORPHA:3286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0001645	ORPHA:3286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3286	Catecholaminergic polymorphic ventricular tachycardia		HP:0001663	ORPHA:3286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001654	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001824	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001945	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002617	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002633	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0012089	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0012378	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0100545	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0100735	ORPHA:3287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0000822	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001250	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001324	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001369	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001646	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001658	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001903	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001920	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002039	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002076	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002092	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002315	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0003326	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0003565	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0004417	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0004970	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0012649	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0020141	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0032554	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0100749	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0100758	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0200042	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:6000944	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:6000945	ORPHA:3287	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0000488	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0000505	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001297	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001635	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001644	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0001659	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002094	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002105	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002167	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002321	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002326	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002637	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0002829	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0004306	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0004372	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0005244	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0011227	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0012219	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0030166	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0033834	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3287	Takayasu arteritis		HP:0100576	ORPHA:3287	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0007663	ORPHA:209943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0007906	ORPHA:209943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0100832	ORPHA:209943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0000501	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0000541	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0000613	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0000622	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0000648	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0001147	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0007917	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209943	IRVAN syndrome		HP:0040049	ORPHA:209943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000003	ORPHA:3270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000164	ORPHA:3270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000174	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000256	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000268	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000275	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000364	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000411	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000426	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000448	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000486	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000670	ORPHA:3270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0000767	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0001252	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0001263	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0001288	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0002167	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0002974	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0003011	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3270	Radioulnar synostosis-developmental delay-hypotonia syndrome		HP:0007477	ORPHA:3270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000708	ORPHA:300305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000718	ORPHA:300305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000750	ORPHA:300305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0001249	ORPHA:300305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0001263	ORPHA:300305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0001999	ORPHA:300305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000319	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000343	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000358	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000400	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000463	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0000664	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0001176	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0001250	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0001513	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0002553	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0011094	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300305	11p15.4 microduplication syndrome		HP:0012389	ORPHA:300305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0001263	ORPHA:263410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0002134	ORPHA:263410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0012697	ORPHA:263410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0000711	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0000737	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0001250	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0001251	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0001260	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0001289	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0001332	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0001347	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0002273	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0002329	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0002465	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0007105	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0007185	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0012747	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0030215	ORPHA:263410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0000494	ORPHA:263410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0002093	ORPHA:263410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0002133	ORPHA:263410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0002510	ORPHA:263410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0004302	ORPHA:263410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0008947	ORPHA:263410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263410	Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome		HP:0012469	ORPHA:263410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001999	ORPHA:84064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002041	ORPHA:84064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002224	ORPHA:84064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002721	ORPHA:84064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000316	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000337	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000431	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001256	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001263	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001392	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001394	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001395	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001511	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001518	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002240	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002299	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0003139	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0004322	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0005599	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0009886	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0011121	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0011220	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0011473	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0025156	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0030056	ORPHA:84064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000957	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000958	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001627	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001888	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001894	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002583	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002719	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0005263	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0011031	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0011877	ORPHA:84064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000023	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000089	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000113	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000501	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000778	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0000821	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001629	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001631	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001636	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001643	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001647	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001659	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0001744	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0002884	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0004969	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0007513	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84064	Syndromic diarrhea		HP:0025085	ORPHA:84064	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0000365	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0000768	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0001762	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0002650	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0002938	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0002945	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0002948	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0003498	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0006297	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0008368	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0009702	ORPHA:3275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0000175	ORPHA:3275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0000470	ORPHA:3275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0001216	ORPHA:3275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0001763	ORPHA:3275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0002007	ORPHA:3275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3275	Spondylocarpotarsal synostosis		HP:0002750	ORPHA:3275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0001382	ORPHA:486815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0002747	ORPHA:486815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0003458	ORPHA:486815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0007502	ORPHA:486815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0000218	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0000467	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0000767	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0000958	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0001270	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0001290	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0002020	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0002205	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0002421	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0002650	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0003306	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0003557	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0003687	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0003690	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0003789	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0010647	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0011471	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0011968	ORPHA:486815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0000028	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0000750	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0000823	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0001612	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0002828	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0008081	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0008180	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486815	Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome		HP:0025502	ORPHA:486815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0000639	ORPHA:423296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0001260	ORPHA:423296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0002066	ORPHA:423296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0001288	ORPHA:423296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0000514	ORPHA:423296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0001272	ORPHA:423296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0003474	ORPHA:423296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0009830	ORPHA:423296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0002460	ORPHA:423296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0000708	ORPHA:423296	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:423296	Spinocerebellar ataxia type 38		HP:0001337	ORPHA:423296	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000028	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000189	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000268	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000269	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000308	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000316	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000325	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000358	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001252	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001263	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001276	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001510	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001511	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001539	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001629	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001631	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0003275	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0004097	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0004322	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0004326	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0010864	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0030680	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0100490	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0100543	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0100810	ORPHA:3380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000008	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000085	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000126	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000175	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000235	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000248	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000252	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000286	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000453	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000581	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000776	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001195	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001250	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001561	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001762	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001792	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002020	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002023	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002032	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002190	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002750	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002871	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0003272	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0004646	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0007598	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0008872	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0010557	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0010880	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0010935	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0100335	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0100790	ORPHA:3380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000518	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000568	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000612	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000772	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0000879	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001188	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001321	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0001360	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002021	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002308	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002323	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002414	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002814	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0002817	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0006501	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0007370	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0007703	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3380	Trisomy 18 syndrome		HP:0007957	ORPHA:3380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0000722	ORPHA:238446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0000750	ORPHA:238446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0001249	ORPHA:238446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0001252	ORPHA:238446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0001263	ORPHA:238446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0007018	ORPHA:238446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0000717	ORPHA:238446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0001250	ORPHA:238446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0002186	ORPHA:238446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0004209	ORPHA:238446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0000256	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0000286	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0000298	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0000494	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0001251	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0004322	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0001382	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0006101	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238446	15q11q13 microduplication syndrome		HP:0030680	ORPHA:238446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000508	ORPHA:502430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000286	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000289	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000356	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000494	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000729	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000750	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0001252	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0001270	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0002263	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0002553	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0003196	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0005274	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0005487	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0011968	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0012758	ORPHA:502430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000028	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000316	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000365	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000369	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000824	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0000954	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0001627	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0002870	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0004209	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0006989	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0033454	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0040064	ORPHA:502430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502430	Weiss-Kruszka Syndrome		HP:0009623	ORPHA:502430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001660	ORPHA:3384	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0000961	ORPHA:3384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001627	ORPHA:3384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001649	ORPHA:3384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001654	ORPHA:3384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0031653	ORPHA:3384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001511	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001629	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001640	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001659	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001667	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0002789	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0011660	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0012020	ORPHA:3384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0000778	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0000849	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001631	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001636	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001642	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001643	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001999	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0002089	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0002101	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0004415	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0004935	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0005301	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0006704	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0011611	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0011640	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0025575	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0031632	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0045060	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0100598	ORPHA:3384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0001669	ORPHA:3384	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0004971	ORPHA:3384	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3384	Common arterial trunk		HP:0031635	ORPHA:3384	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000028	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000160	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000164	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000316	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000343	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000365	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000430	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000431	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000457	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000486	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000490	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000494	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0000508	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001387	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001508	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001510	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001557	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001561	ORPHA:2053	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001562	ORPHA:2053	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001611	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0001762	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0002047	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0002167	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0002650	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0004322	ORPHA:2053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0008872	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0009465	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0010489	ORPHA:2053	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0010751	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0100490	ORPHA:2053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2053	Freeman-Sheldon syndrome		HP:0100790	ORPHA:2053	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001298	ORPHA:83597	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0007204	ORPHA:83597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0007305	ORPHA:83597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0010845	ORPHA:83597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0000708	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0000737	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001250	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001251	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001268	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001317	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001945	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002018	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002134	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002143	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002181	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002315	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002518	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002922	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0007256	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0012486	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0012696	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0012747	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0025373	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0031696	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0032492	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0100786	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0200149	ORPHA:83597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0000572	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0000718	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001259	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001269	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001289	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0001324	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002013	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0002167	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0003474	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0004887	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0006824	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0010843	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0011151	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0011193	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0030857	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0031179	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0100653	ORPHA:83597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0004305	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0006562	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0006597	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0007103	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0012302	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0020088	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0020089	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0031693	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83597	Acute disseminated encephalomyelitis		HP:0031695	ORPHA:83597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0002023	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0002025	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0005105	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0005280	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000377	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0008736	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0008749	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0010297	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0010458	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0012732	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000028	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000047	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000068	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000202	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000204	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000218	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000252	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000405	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000413	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000430	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000431	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000813	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001249	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001362	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001522	ORPHA:2052	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001537	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001539	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001607	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000079	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000618	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001126	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0006101	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0007925	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0007993	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0008678	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0012725	ORPHA:2052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000046	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000062	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000142	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000148	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000316	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000356	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000358	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000370	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000528	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000568	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000678	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000689	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001602	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0001770	ORPHA:2052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0002084	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0002089	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0002101	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0002475	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0002777	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0003191	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0003422	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0004112	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0004397	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0006610	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0008551	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0010720	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0030680	ORPHA:2052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0000772	ORPHA:2052	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0003183	ORPHA:2052	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2052	Fraser syndrome		HP:0009826	ORPHA:2052	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0000561	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0000695	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001030	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001802	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001817	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0002223	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0002298	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0002878	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0005597	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0031274	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0031538	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0032449	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0100792	ORPHA:158687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0000175	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0000377	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0000924	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001233	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001511	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001562	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001638	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001640	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0001836	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0004209	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0006097	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0006670	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0010705	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158687	Lethal acantholytic erosive disorder		HP:0011039	ORPHA:158687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000262	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000347	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000494	ORPHA:2050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000520	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000592	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000682	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000684	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000772	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0000944	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0001252	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0001263	ORPHA:2050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0001334	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0001511	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0001608	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0002007	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0002645	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0002650	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0002652	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0002757	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0002808	ORPHA:2050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0003312	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0004322	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0001382	ORPHA:2050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0006367	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0006487	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2050	Cole-Carpenter syndrome		HP:0011800	ORPHA:2050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0000079	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0001030	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0001057	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0002013	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0003236	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0003270	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0003341	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0004399	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0007585	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0008066	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0200041	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0200097	ORPHA:158684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0000070	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0000075	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0000096	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0000110	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0000126	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0000795	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0001056	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0001075	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0001371	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0001561	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0003560	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0004552	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0007385	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0007589	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0008404	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0008551	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158684	Epidermolysis bullosa simplex with pyloric atresia		HP:0010477	ORPHA:158684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0000953	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0000989	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0001036	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0003341	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0005585	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0007513	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0007585	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0008066	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0031045	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0031180	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0200037	ORPHA:158681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0000464	ORPHA:158681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0002815	ORPHA:158681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0007599	ORPHA:158681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema		HP:0012221	ORPHA:158681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema	NOT	HP:0000478	ORPHA:158681	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema	NOT	HP:0000972	ORPHA:158681	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema	NOT	HP:0008404	ORPHA:158681	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:158681	Epidermolysis bullosa simplex with circinate migratory erythema	NOT	HP:0200097	ORPHA:158681	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000003	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000028	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000047	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000076	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000126	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000154	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000161	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000175	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000218	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000280	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000316	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000337	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000343	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000347	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000358	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000431	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000463	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000470	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000474	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000568	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000774	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000776	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0000813	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001249	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001250	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001274	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001305	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001539	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001561	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001636	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001671	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001679	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0001804	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002020	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002023	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002089	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002119	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002120	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002247	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002251	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0002566	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0004209	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0004397	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0006610	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0006709	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0007957	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0009882	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0010804	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0011344	ORPHA:2059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0012303	ORPHA:2059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2059	Fryns syndrome		HP:0100335	ORPHA:2059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000154	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000179	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000232	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000252	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000322	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000347	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000426	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0000446	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0001166	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0001249	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0001252	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0001519	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0002650	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0002714	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0002827	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0004322	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0004326	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0001382	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2058	Fryns-Smeets-Thiry syndrome		HP:0006443	ORPHA:2058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000179	ORPHA:2057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000303	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000316	ORPHA:2057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000458	ORPHA:2057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000508	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000565	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000574	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000581	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0000664	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0001291	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0002553	ORPHA:2057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0004322	ORPHA:2057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2057	Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome		HP:0006889	ORPHA:2057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0001252	ORPHA:137754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0001298	ORPHA:137754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0003324	ORPHA:137754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0001250	ORPHA:137754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0001263	ORPHA:137754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0002013	ORPHA:137754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0002104	ORPHA:137754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0003396	ORPHA:137754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0006817	ORPHA:137754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0007370	ORPHA:137754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0000316	ORPHA:137754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0000407	ORPHA:137754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137754	Aminoacylase 1 deficiency		HP:0000445	ORPHA:137754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2056	Essential fructosuria		HP:0011033	ORPHA:2056	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2056	Essential fructosuria		HP:0012379	ORPHA:2056	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2056	Essential fructosuria		HP:0010969	ORPHA:2056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2056	Essential fructosuria		HP:0030272	ORPHA:2056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2056	Essential fructosuria		HP:0031979	ORPHA:2056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2056	Essential fructosuria	NOT	HP:0003074	ORPHA:2056	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0001288	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0001760	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0003477	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0003484	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0007141	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0007220	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0007340	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0011402	ORPHA:99939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0001265	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0001761	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0001884	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0002460	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0003458	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0003474	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0003693	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0003701	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0009046	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0012896	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0030235	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0200101	ORPHA:99939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0001270	ORPHA:99939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0002540	ORPHA:99939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0003376	ORPHA:99939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99939	Autosomal dominant Charcot-Marie-Tooth disease type 2E		HP:0000762	ORPHA:99939	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000707	ORPHA:3385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001262	ORPHA:3385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002360	ORPHA:3385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0006979	ORPHA:3385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0030050	ORPHA:3385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0032323	ORPHA:3385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000741	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000989	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001324	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001433	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001744	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001824	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002240	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002315	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001288	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002494	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002500	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002716	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0003115	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0011442	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0012378	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0012751	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0025145	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0100785	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0410263	ORPHA:3385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000020	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000083	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000140	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000491	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000509	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000651	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000708	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000718	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000737	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000739	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000771	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000789	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000802	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000818	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000847	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000952	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001101	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001266	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001269	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001288	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001337	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001345	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001596	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001709	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002013	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002014	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002018	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002119	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002167	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002304	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002380	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002476	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002829	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0003401	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0003470	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0003474	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0004305	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0004372	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0005521	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0006824	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0007178	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0010831	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0011706	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0011731	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0032367	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0040086	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0100653	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0100660	ORPHA:3385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0000738	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001085	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001250	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001259	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001622	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001635	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0001701	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0002196	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0005268	ORPHA:3385	TAS		HP:0040284			C	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0011675	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0012486	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0012819	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0025475	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3385	African trypanosomiasis		HP:0031258	ORPHA:3385	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0000969	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0000980	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0000988	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0001638	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0001744	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0001907	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0001945	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002014	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002027	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002094	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002240	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002315	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002716	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0003326	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0011355	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0011675	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0012735	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0012819	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0030057	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0100539	ORPHA:3386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0001635	ORPHA:3386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002251	ORPHA:3386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002571	ORPHA:3386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0012700	ORPHA:3386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0000707	ORPHA:3386	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0002383	ORPHA:3386	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3386	American trypanosomiasis		HP:0009830	ORPHA:3386	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000490	ORPHA:502434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001249	ORPHA:502434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001263	ORPHA:502434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000028	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000154	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000426	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000729	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001250	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0002020	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0011968	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0045074	ORPHA:502434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000050	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000085	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000202	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000218	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000252	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000347	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000369	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000486	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000527	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000664	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000954	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0000965	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001252	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001377	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001382	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001508	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001511	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001566	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0001999	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0002650	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0002817	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0004209	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0004322	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0004691	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0010864	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0012444	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502434	STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome		HP:0200134	ORPHA:502434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0001891	ORPHA:99931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0000980	ORPHA:99931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0001433	ORPHA:99931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002105	ORPHA:99931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002113	ORPHA:99931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0012378	ORPHA:99931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0012735	ORPHA:99931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0025179	ORPHA:99931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0001508	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0001640	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0001945	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002091	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002094	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002206	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002240	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002878	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0002923	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0003262	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0003453	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0003493	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0012393	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0025390	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0025392	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0025420	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0030057	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0030148	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0030830	ORPHA:99931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0000099	ORPHA:99931	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99931	Idiopathic pulmonary hemosiderosis		HP:0100327	ORPHA:99931	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0001873	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0001875	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0001892	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0001902	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0001933	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0002090	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0002098	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0003010	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0011883	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0012143	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0012418	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0040223	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238459	SLC35A1-CDG		HP:0100658	ORPHA:238459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0002191	ORPHA:401866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0008288	ORPHA:401866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0000505	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0000639	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0000648	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0000736	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0001264	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0001276	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0001347	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0002317	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0002415	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0002464	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0002928	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0003487	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0008945	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0100561	ORPHA:401866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0000737	ORPHA:401866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0001251	ORPHA:401866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0001290	ORPHA:401866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0001336	ORPHA:401866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0002376	ORPHA:401866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0011968	ORPHA:401866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia		HP:0001712	ORPHA:401866	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia	NOT	HP:0002151	ORPHA:401866	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:401866	Childhood-onset spasticity with hyperglycinemia	NOT	HP:0100543	ORPHA:401866	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0001300	ORPHA:238455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0001332	ORPHA:238455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0000338	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0000737	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0001263	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0001276	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0001344	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0002019	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0002020	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0002067	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0002072	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0002310	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0002375	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0002509	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0004354	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0007256	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0008936	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0010553	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0011968	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238455	Infantile dystonia-parkinsonism		HP:0100021	ORPHA:238455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0000121	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0000164	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0000168	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0000174	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0000230	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0000975	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0000988	ORPHA:53715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0001053	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0001482	ORPHA:53715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0001609	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0001744	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0002240	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0002653	ORPHA:53715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0007470	ORPHA:53715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0008069	ORPHA:53715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0010783	ORPHA:53715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0100249	ORPHA:53715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53715	Familial tumoral calcinosis		HP:0100774	ORPHA:53715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001635	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001640	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001649	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0002875	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0003115	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0005162	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0031664	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0031670	ORPHA:2041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001279	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001627	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001631	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001643	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001647	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001650	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001655	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001681	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0001962	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0002092	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0002617	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0002789	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0005133	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0006689	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0010741	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0011675	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0012764	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0030848	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2041	Coronary arterial fistula		HP:0030882	ORPHA:2041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2040	Congenital respiratory-biliary fistula		HP:0001392	ORPHA:2040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2040	Congenital respiratory-biliary fistula		HP:0002777	ORPHA:2040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0001805	ORPHA:158676	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0001808	ORPHA:158676	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0008404	ORPHA:158676	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0001810	ORPHA:158676	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0008391	ORPHA:158676	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0008401	ORPHA:158676	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0040036	ORPHA:158676	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only		HP:0001802	ORPHA:158676	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only	NOT	HP:0001030	ORPHA:158676	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only	NOT	HP:0008066	ORPHA:158676	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:158676	Localized dystrophic epidermolysis bullosa, nails only	NOT	HP:0011121	ORPHA:158676	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000225	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000324	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000360	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000365	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000421	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000496	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000520	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000572	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0000737	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0001249	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0001250	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0001260	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0001263	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0001269	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0001342	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0002017	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0002138	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0002315	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0002617	ORPHA:53719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0007185	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0007730	ORPHA:53719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0007797	ORPHA:53719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0011276	ORPHA:53719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0100021	ORPHA:53719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0100026	ORPHA:53719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0100659	ORPHA:53719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53719	Cerebrofacial arteriovenous metameric syndrome type 2		HP:0100784	ORPHA:53719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0000613	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0000632	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0000643	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0007663	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0008000	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0009926	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0030953	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0200026	ORPHA:171673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0000491	ORPHA:171673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0000559	ORPHA:171673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0007727	ORPHA:171673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0011494	ORPHA:171673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0011496	ORPHA:171673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0100583	ORPHA:171673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171673	Limbal stem cell deficiency		HP:0500008	ORPHA:171673	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0000963	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0000972	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0000992	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0001009	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0001029	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0001030	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0001056	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0001810	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0002043	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0002814	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0004334	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0007473	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0008066	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0008391	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0010783	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0025474	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0031045	ORPHA:158673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0002815	ORPHA:158673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0008390	ORPHA:158673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158673	Localized dystrophic epidermolysis bullosa, acral form		HP:0009811	ORPHA:158673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0001172	ORPHA:2048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0001250	ORPHA:2048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0001263	ORPHA:2048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0001288	ORPHA:2048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0001344	ORPHA:2048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0001608	ORPHA:2048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0009800	ORPHA:2048	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:2048	Foix-Chavany-Marie syndrome		HP:0100543	ORPHA:2048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000408	ORPHA:2047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000505	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000510	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000518	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000545	ORPHA:2047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000670	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000726	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0000820	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0001250	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0001251	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0001387	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0001596	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002120	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002353	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002376	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002381	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002514	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002621	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002650	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0002808	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0003202	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0004326	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0004334	ORPHA:2047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0005978	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0007328	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0008207	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0009830	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0012062	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0100022	ORPHA:2047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2047	Flynn-Aird syndrome		HP:0200042	ORPHA:2047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99926	Gestational choriocarcinoma		HP:0100768	ORPHA:99926	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99926	Gestational choriocarcinoma		HP:0002664	ORPHA:99926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99926	Gestational choriocarcinoma		HP:0005268	ORPHA:99926	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:99926	Gestational choriocarcinoma		HP:0011433	ORPHA:99926	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:99926	Gestational choriocarcinoma		HP:0031502	ORPHA:99926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99926	Gestational choriocarcinoma		HP:0100608	ORPHA:99926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0000492	ORPHA:2045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0000498	ORPHA:2045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0000499	ORPHA:2045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0000613	ORPHA:2045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0000653	ORPHA:2045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0000787	ORPHA:2045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0001597	ORPHA:2045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0008069	ORPHA:2045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2045	FLOTCH syndrome		HP:0100533	ORPHA:2045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99927	Hydatidiform mole		HP:0000836	ORPHA:99927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99927	Hydatidiform mole		HP:0001903	ORPHA:99927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99927	Hydatidiform mole		HP:0002017	ORPHA:99927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99927	Hydatidiform mole		HP:0005268	ORPHA:99927	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:99927	Hydatidiform mole		HP:0100602	ORPHA:99927	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:99927	Hydatidiform mole		HP:0100878	ORPHA:99927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99927	Hydatidiform mole		HP:0400008	ORPHA:99927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0000273	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0001250	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0001260	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0001328	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002015	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002533	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002788	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0008936	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0030215	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0100022	ORPHA:225147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0000020	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0000298	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0000338	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0000736	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0001288	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0001300	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0001332	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0001347	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002033	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002066	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002067	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002072	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002300	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002301	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002307	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002322	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0002465	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0003487	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0004372	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0005366	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0007158	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0007185	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0007359	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0008947	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0011151	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0025439	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0030187	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:225147	Sporadic infantile bilateral striatal necrosis		HP:0040288	ORPHA:225147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0000590	ORPHA:352470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0003325	ORPHA:352470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0000716	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0001288	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0001290	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0001533	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0001558	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0001288	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0002828	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0002870	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0002875	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0003198	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0003307	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0003326	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0003391	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0003394	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0003737	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0004673	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0007970	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0008331	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352470	DNA2-related mitochondrial DNA deletion syndrome		HP:0040013	ORPHA:352470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99928	Placental site trophoblastic tumor		HP:0000141	ORPHA:99928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99928	Placental site trophoblastic tumor		HP:0005268	ORPHA:99928	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:99928	Placental site trophoblastic tumor		HP:0011434	ORPHA:99928	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:99928	Placental site trophoblastic tumor		HP:0100608	ORPHA:99928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001518	ORPHA:2044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0004322	ORPHA:2044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0011098	ORPHA:2044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000154	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000325	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000470	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000486	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000750	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000914	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001256	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001510	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0002342	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0002750	ORPHA:2044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000028	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000047	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000104	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000107	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000121	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000126	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000322	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000327	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000369	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000405	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000446	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000455	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000490	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000540	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000670	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000677	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000691	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000711	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000718	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000722	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000736	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000739	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000826	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000878	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000894	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001156	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001250	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001260	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001344	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001385	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001611	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001620	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0002019	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0002020	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0002136	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0002751	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0003037	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0003083	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0003189	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0003879	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0005743	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0006335	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0007018	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0009765	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0009778	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0010049	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0010946	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0010957	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0011300	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0012871	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0025160	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0030084	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0030424	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0040288	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0100710	ORPHA:2044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000113	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0000593	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001631	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001636	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0001680	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0002608	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0003774	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0005301	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0008554	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0011599	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2044	Floating-Harbor syndrome		HP:0012538	ORPHA:2044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0002094	ORPHA:275766	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0001667	ORPHA:275766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0002092	ORPHA:275766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0004890	ORPHA:275766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0005317	ORPHA:275766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:3000042	ORPHA:275766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0001279	ORPHA:275766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0001635	ORPHA:275766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0001785	ORPHA:275766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0005180	ORPHA:275766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0012098	ORPHA:275766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0030148	ORPHA:275766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0100749	ORPHA:275766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0001962	ORPHA:275766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0002105	ORPHA:275766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension		HP:0010741	ORPHA:275766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension	NOT	HP:0003549	ORPHA:275766	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:275766	Idiopathic pulmonary arterial hypertension	NOT	HP:0004870	ORPHA:275766	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000161	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000235	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000256	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000268	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000316	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000482	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000534	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000581	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000615	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000951	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0001561	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0001601	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0100629	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000175	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000324	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0000612	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0002007	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3374	Unilateral ocular duplication		HP:0002084	ORPHA:3374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0000127	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0008207	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0000952	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0000989	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0000991	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001114	ORPHA:275761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001263	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001297	ORPHA:275761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001395	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001399	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001410	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001414	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001433	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001508	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001541	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001824	ORPHA:275761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001903	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001922	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001941	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001944	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001971	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002013	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002014	ORPHA:275761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002017	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002027	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002040	ORPHA:275761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002092	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002153	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002155	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002361	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002570	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002615	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002902	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0002910	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0003124	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0003155	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0003270	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0012605	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0004326	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0004333	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0004395	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0004416	ORPHA:275761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0001677	ORPHA:275761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0006583	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0010512	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0011106	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0011968	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0012598	ORPHA:275761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275761	Lysosomal acid lipase deficiency		HP:0100543	ORPHA:275761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0002916	ORPHA:3375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000098	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000286	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000750	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001263	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001270	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001328	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0002019	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0002027	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0004209	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0008947	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0100543	ORPHA:3375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000003	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000316	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000582	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000716	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000739	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000767	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000869	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001249	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001250	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001337	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001385	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001629	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001631	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0002960	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0001382	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0007018	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0008209	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0008678	ORPHA:3375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3375	Trisomy X syndrome		HP:0000826	ORPHA:3375	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000028	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000047	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000062	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000154	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000158	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000160	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000175	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000235	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000238	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000256	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000316	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000347	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000358	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000470	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000518	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000612	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0000774	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0001360	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0001511	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0001539	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0001561	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0001671	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0001732	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0002240	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0002435	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0002566	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0002916	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0004331	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0005264	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0006101	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0007370	ORPHA:3376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0008056	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0008736	ORPHA:3376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3376	Triploidy syndrome		HP:0100335	ORPHA:3376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0004322	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000233	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000252	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000286	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000311	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000316	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000319	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000347	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0000369	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0001249	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0001250	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0001263	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0005280	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0007370	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36367	Distal deletion 1q syndrome		HP:0011220	ORPHA:36367	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3377	Trismus-pseudocamptodactyly syndrome		HP:0000303	ORPHA:3377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3377	Trismus-pseudocamptodactyly syndrome		HP:0001376	ORPHA:3377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3377	Trismus-pseudocamptodactyly syndrome		HP:0002827	ORPHA:3377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3377	Trismus-pseudocamptodactyly syndrome		HP:0003011	ORPHA:3377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3377	Trismus-pseudocamptodactyly syndrome		HP:0004322	ORPHA:3377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3377	Trismus-pseudocamptodactyly syndrome		HP:0009773	ORPHA:3377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3377	Trismus-pseudocamptodactyly syndrome		HP:0000508	ORPHA:3377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99925	Invasive mole		HP:0011433	ORPHA:99925	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:99925	Invasive mole		HP:0400008	ORPHA:99925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000161	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000175	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000235	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000272	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000369	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000476	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000528	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000568	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000601	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001162	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001250	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001252	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001511	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001629	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001631	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001643	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001789	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0002167	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0002644	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0007598	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0010864	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0011344	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0030680	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0100543	ORPHA:3378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000008	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000028	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000069	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000126	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000164	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000343	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000370	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000384	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000407	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000478	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000490	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000499	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000504	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000518	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000612	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000648	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000772	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0000774	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0001362	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0002101	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0002308	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0002650	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0002705	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0002808	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0004467	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0005306	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0005562	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0007477	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0008046	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0008053	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0009738	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0011039	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0100257	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0100627	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3378	Trisomy 13 syndrome		HP:0100790	ORPHA:3378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0003325	ORPHA:352479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0030046	ORPHA:352479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0000158	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0001626	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0002792	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0003202	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0003707	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0008994	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0008997	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0030234	ORPHA:352479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0002505	ORPHA:352479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0003326	ORPHA:352479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0003691	ORPHA:352479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0008305	ORPHA:352479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0000478	ORPHA:352479	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352479	ISPD-related limb-girdle muscular dystrophy R20		HP:0011446	ORPHA:352479	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001263	ORPHA:3379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0010864	ORPHA:3379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000028	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000076	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000154	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000175	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000218	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000219	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000252	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000286	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000316	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000322	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000347	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000358	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000581	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000768	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001161	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001761	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001822	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0002000	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0002007	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0002162	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0002572	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0002857	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0003510	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0004322	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0005280	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0008905	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0009911	ORPHA:3379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000075	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000411	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0000752	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001166	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001250	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001321	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001382	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001627	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001747	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0001845	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0002650	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0006897	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3379	Distal duplication 17q syndrome		HP:0008619	ORPHA:3379	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0000498	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0001805	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0003765	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0005406	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0008396	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0010783	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0011131	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0011228	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0011354	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0012390	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0025085	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0031123	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0040181	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0040189	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0100038	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0200039	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0410017	ORPHA:294023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294023	Neonatal inflammatory skin and bowel disease		HP:0001712	ORPHA:294023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001058	ORPHA:99921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001072	ORPHA:99921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0007432	ORPHA:99921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0000217	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0000495	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0000613	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001000	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001097	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001596	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001806	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002110	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002719	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002910	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0008404	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0010783	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0012537	ORPHA:99921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0000142	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0000790	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001324	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001369	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001371	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001541	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001741	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001824	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0001876	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002014	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002015	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002018	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002020	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002027	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002031	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002039	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002043	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002094	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002107	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002113	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002202	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0002829	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0003326	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0004791	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0006536	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0011946	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0012181	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0012344	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0012531	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0012735	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0025270	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0030828	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0100537	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0100577	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0100749	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0200037	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99921	Chronic graft versus host disease		HP:0200042	ORPHA:99921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48372	Nodular regenerative hyperplasia of the liver		HP:0001409	ORPHA:48372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48372	Nodular regenerative hyperplasia of the liver		HP:0006707	ORPHA:48372	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0000958	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0002208	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0002209	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0002299	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0002552	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0003777	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0009886	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0045075	ORPHA:3361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0001596	ORPHA:3361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3361	Trichodysplasia-xeroderma syndrome		HP:0002231	ORPHA:3361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000003	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000107	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000162	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000364	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000358	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000411	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000430	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000463	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000478	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000486	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000504	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000505	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000508	ORPHA:2031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000567	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000581	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0000639	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0001249	ORPHA:2031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0001250	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0001276	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0002093	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0002119	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0002435	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0002612	ORPHA:2031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0003196	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0004209	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0004322	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0004422	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0007477	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2031	Hepatic fibrosis-renal cysts-intellectual disability syndrome		HP:0100022	ORPHA:2031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0000407	ORPHA:47045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0000509	ORPHA:47045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0000975	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0000989	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0001025	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0001369	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0001944	ORPHA:47045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0001945	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0001959	ORPHA:47045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0002017	ORPHA:47045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0002027	ORPHA:47045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0002315	ORPHA:47045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0002829	ORPHA:47045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0003326	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0010783	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0012378	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47045	Familial cold urticaria		HP:0012534	ORPHA:47045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0000821	ORPHA:48377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0000836	ORPHA:48377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0000953	ORPHA:48377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0000989	ORPHA:48377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0001370	ORPHA:48377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0002725	ORPHA:48377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0002960	ORPHA:48377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0006775	ORPHA:48377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0010702	ORPHA:48377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0010783	ORPHA:48377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48377	Subcorneal pustular dermatosis		HP:0200039	ORPHA:48377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001009	ORPHA:2038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0004952	ORPHA:2038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001892	ORPHA:2038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0002094	ORPHA:2038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0002140	ORPHA:2038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0002326	ORPHA:2038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0012151	ORPHA:2038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0012418	ORPHA:2038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0000421	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0000961	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001217	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001658	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001891	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001962	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001977	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0002076	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0002092	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0002105	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0006689	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0011919	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0012735	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0030049	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0030148	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0040223	ORPHA:2038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0001250	ORPHA:2038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0002722	ORPHA:2038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0005244	ORPHA:2038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2038	Pulmonary arteriovenous malformation		HP:0100523	ORPHA:2038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000385	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000951	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0001965	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0006709	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0008070	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0008551	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0009738	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0011251	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0011272	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0100783	ORPHA:2036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000010	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000164	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000506	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000518	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000684	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000822	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0001231	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0100540	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0100651	ORPHA:2036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000073	ORPHA:2036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000077	ORPHA:2036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000625	ORPHA:2036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0000966	ORPHA:2036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0005580	ORPHA:2036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2036	Scalp-ear-nipple syndrome		HP:0012330	ORPHA:2036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0002583	ORPHA:35062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0033431	ORPHA:35062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0000554	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0001287	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0001824	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0001945	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0002017	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0002027	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0002039	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0002090	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0006515	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0012115	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0012486	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0032118	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0033993	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0430087	ORPHA:35062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0000572	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0000979	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0000988	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0001289	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0001733	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0001873	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0001878	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0003326	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0004936	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0012223	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0012378	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0025143	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35062	Severe disseminated cytomegalovirus infection in immunocompetent patients		HP:0033117	ORPHA:35062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0000750	ORPHA:209908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002167	ORPHA:209908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0001260	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0001328	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002465	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002474	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002546	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0006977	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0007010	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0010863	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0011098	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0031434	ORPHA:209908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002307	ORPHA:209908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002339	ORPHA:209908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002340	ORPHA:209908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0007015	ORPHA:209908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0011968	ORPHA:209908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0012434	ORPHA:209908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0000176	ORPHA:209908	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0000396	ORPHA:209908	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0000729	ORPHA:209908	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0002705	ORPHA:209908	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209908	Isolated childhood apraxia of speech		HP:0011228	ORPHA:209908	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0001004	ORPHA:2035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0002716	ORPHA:2035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0003550	ORPHA:2035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0100763	ORPHA:2035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000953	ORPHA:2035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000962	ORPHA:2035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0002840	ORPHA:2035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0012224	ORPHA:2035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0012378	ORPHA:2035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0012531	ORPHA:2035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0032061	ORPHA:2035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000034	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000045	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000077	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0001945	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0002088	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0002091	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0012735	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0030828	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0031690	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0031842	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0032260	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0100673	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0100796	ORPHA:2035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000031	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000093	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000099	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000100	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000790	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0000796	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0001785	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0005086	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2035	Lymphatic filariasis		HP:0008763	ORPHA:2035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0006530	ORPHA:2032	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0001063	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0002020	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0002110	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0002206	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0002875	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0012378	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0012735	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0025175	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0025179	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0025390	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0030830	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0031631	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0031950	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0032341	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0045051	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0100759	ORPHA:2032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0003546	ORPHA:2032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0010444	ORPHA:2032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2032	Idiopathic pulmonary fibrosis		HP:0033367	ORPHA:2032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000546	ORPHA:3363	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000135	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000527	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000580	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000821	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000824	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0001249	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0001251	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0001510	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0001518	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0001596	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0002750	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0003265	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0008070	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0009830	ORPHA:3363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000028	ORPHA:3363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000054	ORPHA:3363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000164	ORPHA:3363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000545	ORPHA:3363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0002007	ORPHA:3363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0000252	ORPHA:3363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3363	Trichomegaly-retina pigmentary degeneration-dwarfism syndrome		HP:0001250	ORPHA:3363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001272	ORPHA:35069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002361	ORPHA:35069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002376	ORPHA:35069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000648	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000649	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001251	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001268	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001285	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001347	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002191	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002317	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002454	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002483	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002500	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0003134	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0003405	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0003444	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0003477	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0007141	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0007256	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0008936	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0009830	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0012675	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0012698	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0025435	ORPHA:35069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000486	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000618	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000639	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000708	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000712	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000729	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000736	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000750	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0000752	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001257	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001260	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001288	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001332	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001371	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002019	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0002307	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0005968	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0011951	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0012043	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0012332	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0100710	ORPHA:35069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0001250	ORPHA:35069	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0005949	ORPHA:35069	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0010545	ORPHA:35069	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0025331	ORPHA:35069	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0030842	ORPHA:35069	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35069	Infantile neuroaxonal dystrophy		HP:0031358	ORPHA:35069	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0000243	ORPHA:3366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0011330	ORPHA:3366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0000336	ORPHA:3366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0000341	ORPHA:3366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0000431	ORPHA:3366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0000601	ORPHA:3366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0000664	ORPHA:3366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0002553	ORPHA:3366	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0000750	ORPHA:3366	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0001539	ORPHA:3366	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0001085	ORPHA:3366	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3366	Non-syndromic metopic craniosynostosis		HP:0002516	ORPHA:3366	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000021	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000047	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000076	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000252	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000465	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000668	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000722	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000736	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000752	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000829	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001274	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001655	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001955	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001999	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002099	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002206	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002360	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002389	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002527	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002679	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002878	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0004322	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0030082	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0100738	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0100753	ORPHA:209905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000820	ORPHA:209905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000707	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000851	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001251	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001266	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002072	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002086	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002098	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002643	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0008947	ORPHA:209905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0000407	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001256	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001260	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001263	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001270	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001332	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001336	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001508	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001510	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001629	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001631	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0001671	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002080	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002092	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002186	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002205	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002311	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002312	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0002925	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0004305	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0006530	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0006532	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0008188	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0008223	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209905	Brain-lung-thyroid syndrome		HP:0011780	ORPHA:209905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0001396	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0001397	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0001403	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0002155	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0003124	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0003141	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0006573	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0011980	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0012115	ORPHA:209902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0001513	ORPHA:209902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0001677	ORPHA:209902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0004943	ORPHA:209902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0008372	ORPHA:209902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0012397	ORPHA:209902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209902	Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency		HP:0100514	ORPHA:209902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000243	ORPHA:3369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0001263	ORPHA:3369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0004322	ORPHA:3369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000023	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000216	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000218	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000237	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000286	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000341	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000358	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000431	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000601	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0001250	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0001518	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0001629	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0002342	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0000444	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0005484	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0005494	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0005495	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0005769	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0008897	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3369	Trigonocephaly-short stature-developmental delay syndrome		HP:0011324	ORPHA:3369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000709	ORPHA:36397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000716	ORPHA:36397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000739	ORPHA:36397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0001482	ORPHA:36397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0001513	ORPHA:36397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002829	ORPHA:36397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0012378	ORPHA:36397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0001031	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002027	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002215	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002225	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0003119	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0003270	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0003565	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0007596	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0011227	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0012532	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0025406	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0025502	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0031905	ORPHA:36397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000217	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000819	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000821	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000822	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000958	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0000978	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0001250	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0001369	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0001581	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002014	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002019	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002315	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002354	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002360	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002376	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0002960	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0003401	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0009830	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0034265	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36397	Adiposis dolorosa		HP:0100585	ORPHA:36397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3350	Tremor-nystagmus-duodenal ulcer syndrome		HP:0000639	ORPHA:3350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3350	Tremor-nystagmus-duodenal ulcer syndrome		HP:0002588	ORPHA:3350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3350	Tremor-nystagmus-duodenal ulcer syndrome		HP:0100022	ORPHA:3350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3350	Tremor-nystagmus-duodenal ulcer syndrome		HP:0001251	ORPHA:3350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001252	ORPHA:2020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0003323	ORPHA:2020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0011807	ORPHA:2020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0000218	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0000678	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001270	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001284	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001315	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001371	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001508	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001824	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002015	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002058	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002086	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002421	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002747	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0003388	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0004347	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0004396	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0011842	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0011968	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0012378	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0030192	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0030319	ORPHA:2020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0000276	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0000347	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0000602	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0000767	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001374	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001558	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001561	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001609	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001627	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001648	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001761	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0001762	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002205	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002315	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002360	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002650	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002751	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002878	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0002987	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0003273	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0003307	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0003324	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0003547	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0003749	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0004878	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0005216	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0006380	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0006466	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0009004	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0009027	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0011470	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0011951	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0012416	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0012418	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2020	Congenital fiber-type disproportion myopathy		HP:0012785	ORPHA:2020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0001250	ORPHA:306550	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0001298	ORPHA:306550	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0001410	ORPHA:306550	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0001395	ORPHA:306550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0002059	ORPHA:306550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0001629	ORPHA:306550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0004935	ORPHA:306550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306550	FADD-related immunodeficiency		HP:0030057	ORPHA:306550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000750	ORPHA:352490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001249	ORPHA:352490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001999	ORPHA:352490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000160	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000252	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000286	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000316	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000322	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000347	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000369	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000431	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000486	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000520	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000722	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000729	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000733	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001263	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001290	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001328	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001488	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001518	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0002553	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0004322	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0008762	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0008872	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0012745	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0025112	ORPHA:352490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000023	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000028	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000278	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000463	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000582	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000752	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0000964	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001250	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001257	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001276	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001347	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001537	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001627	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001631	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0001760	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0002650	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0002803	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0002804	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0002808	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0004283	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0005274	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0006184	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0007018	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0009183	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0009473	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0012443	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0100021	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352490	Autism spectrum disorder due to AUTS2 deficiency		HP:0100277	ORPHA:352490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0000169	ORPHA:2028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0000212	ORPHA:2028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0000271	ORPHA:2028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0000929	ORPHA:2028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0000940	ORPHA:2028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0001387	ORPHA:2028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0001482	ORPHA:2028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0001522	ORPHA:2028	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0001595	ORPHA:2028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0002797	ORPHA:2028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0003202	ORPHA:2028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0005876	ORPHA:2028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0008065	ORPHA:2028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0011024	ORPHA:2028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0200034	ORPHA:2028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2028	Juvenile hyaline fibromatosis		HP:0200042	ORPHA:2028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2027	Gingival fibromatosis-progressive deafness syndrome		HP:0000169	ORPHA:2027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2027	Gingival fibromatosis-progressive deafness syndrome		HP:0000212	ORPHA:2027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2027	Gingival fibromatosis-progressive deafness syndrome		HP:0000407	ORPHA:2027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2027	Gingival fibromatosis-progressive deafness syndrome		HP:0000684	ORPHA:2027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0000164	ORPHA:2026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0000169	ORPHA:2026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0000212	ORPHA:2026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0000280	ORPHA:2026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0000574	ORPHA:2026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0000664	ORPHA:2026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0000684	ORPHA:2026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0001007	ORPHA:2026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0001250	ORPHA:2026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0001251	ORPHA:2026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0002230	ORPHA:2026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0002353	ORPHA:2026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2026	Gingival fibromatosis-hypertrichosis syndrome		HP:0100543	ORPHA:2026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000169	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000212	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000218	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000232	ORPHA:2025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000256	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000316	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000430	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000494	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000574	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000664	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0000684	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0002263	ORPHA:2025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0005280	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2025	Gingival fibromatosis-facial dysmorphism syndrome		HP:0006482	ORPHA:2025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2024	Hereditary gingival fibromatosis		HP:0000169	ORPHA:2024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2024	Hereditary gingival fibromatosis		HP:0000212	ORPHA:2024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0002585	ORPHA:2023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0002814	ORPHA:2023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0030448	ORPHA:2023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0001945	ORPHA:2023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0003011	ORPHA:2023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0001824	ORPHA:2023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0002039	ORPHA:2023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0002817	ORPHA:2023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2023	Undifferentiated pleomorphic sarcoma		HP:0012378	ORPHA:2023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0000174	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0000347	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0000358	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0000506	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0001635	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0001723	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0001852	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0001943	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0011039	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0030680	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0100543	ORPHA:2022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0000028	ORPHA:2022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0000830	ORPHA:2022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0001250	ORPHA:2022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0008736	ORPHA:2022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2022	Endocardial fibroelastosis		HP:0001706	ORPHA:2022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000160	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000175	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000260	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000311	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000316	ORPHA:2021	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000364	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000369	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000463	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000470	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000494	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000520	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000772	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000773	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000774	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000882	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000885	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000940	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0000944	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0001156	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0001357	ORPHA:2021	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0001539	ORPHA:2021	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0001591	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0001804	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0002093	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0002983	ORPHA:2021	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0003312	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0004322	ORPHA:2021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0005280	ORPHA:2021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2021	Fibrochondrogenesis		HP:0100490	ORPHA:2021	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0000264	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0000268	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0000679	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0000687	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0000691	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0001597	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0001808	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0002007	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0006285	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0009722	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0011001	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0011362	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0030312	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0030758	ORPHA:3352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0006485	ORPHA:3352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3352	Tricho-dento-osseous syndrome		HP:0040019	ORPHA:3352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0000008	ORPHA:3353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0000684	ORPHA:3353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0000982	ORPHA:3353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0002209	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0002213	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0002299	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0002650	ORPHA:3353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0003272	ORPHA:3353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0003307	ORPHA:3353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0005338	ORPHA:3353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0006482	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0007565	ORPHA:3353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0008069	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0008499	ORPHA:3353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0011069	ORPHA:3353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0100840	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0009720	ORPHA:3353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0009804	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3353	Trichodermodysplasia-dental alterations syndrome		HP:0200102	ORPHA:3353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0011923	ORPHA:99901	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001290	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001298	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001397	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001508	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001635	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001639	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001644	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001873	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001987	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0002151	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0002910	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003128	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003198	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003234	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003324	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003326	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003458	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003473	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0008151	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0008331	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0025435	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0045045	ORPHA:99901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001645	ORPHA:99901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0001958	ORPHA:99901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0002181	ORPHA:99901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0003215	ORPHA:99901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0006554	ORPHA:99901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99901	Acyl-CoA dehydrogenase 9 deficiency		HP:0011695	ORPHA:99901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000218	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000276	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000347	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000365	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000601	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000716	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000739	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000750	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000767	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000786	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000836	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000870	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001256	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001265	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001270	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001290	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001310	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001321	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001337	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001510	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001761	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0002073	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0002075	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0001288	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0002650	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0002750	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0002761	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0003326	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0003391	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0003458	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0003474	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0003557	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0003701	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0003737	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0004322	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0008180	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0009051	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0012032	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0012240	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0030319	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0030890	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0100874	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0100887	ORPHA:502423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000729	ORPHA:502423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0100753	ORPHA:502423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000543	ORPHA:502423	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome		HP:0000580	ORPHA:502423	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002197	ORPHA:36387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002121	ORPHA:36387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002373	ORPHA:36387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0001251	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0001252	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002069	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002123	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002311	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002376	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002539	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0007010	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0007058	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0010819	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0010850	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0011151	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0100543	ORPHA:36387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0000729	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0000739	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0001337	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0001763	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002067	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002133	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0002384	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0003066	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0004684	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0007359	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0008770	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36387	Genetic epilepsy with febrile seizure plus		HP:0100694	ORPHA:36387	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002540	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002754	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002756	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002821	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0003693	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0007002	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0012735	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0100287	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0001324	ORPHA:36386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002141	ORPHA:36386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002270	ORPHA:36386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002936	ORPHA:36386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0007078	ORPHA:36386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0031060	ORPHA:36386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0000962	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0001026	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0001058	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002460	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0003376	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0006937	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0007021	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0007550	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0009027	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0009763	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0010829	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0010834	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0200042	ORPHA:36386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0000365	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36386	Hereditary sensory and autonomic neuropathy type 1		HP:0002020	ORPHA:36386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99981	Apnea of prematurity		HP:0002104	ORPHA:99981	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99981	Apnea of prematurity		HP:0000961	ORPHA:99981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99981	Apnea of prematurity		HP:0001662	ORPHA:99981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99981	Apnea of prematurity		HP:0012418	ORPHA:99981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99981	Apnea of prematurity		HP:0001531	ORPHA:99981	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0001744	ORPHA:52416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0001824	ORPHA:52416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0002039	ORPHA:52416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0002716	ORPHA:52416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0005561	ORPHA:52416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0011024	ORPHA:52416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0012378	ORPHA:52416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0001945	ORPHA:52416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52416	Mantle cell lymphoma		HP:0012191	ORPHA:52416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85336	X-linked neurodegenerative syndrome, Hamel type		HP:0000618	ORPHA:85336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85336	X-linked neurodegenerative syndrome, Hamel type		HP:0001250	ORPHA:85336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85336	X-linked neurodegenerative syndrome, Hamel type		HP:0001257	ORPHA:85336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85336	X-linked neurodegenerative syndrome, Hamel type		HP:0001263	ORPHA:85336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85336	X-linked neurodegenerative syndrome, Hamel type		HP:0001522	ORPHA:85336	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:85336	X-linked neurodegenerative syndrome, Hamel type		HP:0010864	ORPHA:85336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0000505	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0000614	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0000820	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0001824	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0001903	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0001945	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0002017	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0002027	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0002113	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0002205	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0002716	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0012191	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0012378	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0100721	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0000975	ORPHA:52417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0002019	ORPHA:52417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52417	MALT lymphoma		HP:0012123	ORPHA:52417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0012533	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0030016	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0030155	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0030943	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0032150	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0033345	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0100515	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0100518	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0100639	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0500005	ORPHA:60039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0034267	ORPHA:60039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0034805	ORPHA:60039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome		HP:0034806	ORPHA:60039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome	NOT	HP:0000989	ORPHA:60039	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome	NOT	HP:0001311	ORPHA:60039	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome	NOT	HP:0003474	ORPHA:60039	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome	NOT	HP:0007379	ORPHA:60039	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome	NOT	HP:0010787	ORPHA:60039	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:60039	Pudendal nerve entrapment syndrome	NOT	HP:0030439	ORPHA:60039	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:85338	X-linked intellectual disability-ataxia-apraxia syndrome		HP:0001250	ORPHA:85338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85338	X-linked intellectual disability-ataxia-apraxia syndrome		HP:0001251	ORPHA:85338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85338	X-linked intellectual disability-ataxia-apraxia syndrome		HP:0001256	ORPHA:85338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85338	X-linked intellectual disability-ataxia-apraxia syndrome		HP:0001762	ORPHA:85338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85338	X-linked intellectual disability-ataxia-apraxia syndrome		HP:0002186	ORPHA:85338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85332	X-linked intellectual disability-retinitis pigmentosa syndrome		HP:0001249	ORPHA:85332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85332	X-linked intellectual disability-retinitis pigmentosa syndrome		HP:0007730	ORPHA:85332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0000608	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0001249	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0001251	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0001263	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0001274	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0001290	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0001522	ORPHA:85334	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0002123	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0006538	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85334	X-linked neurodegenerative syndrome, Bertini type		HP:0200134	ORPHA:85334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0001609	ORPHA:60032	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0001618	ORPHA:60032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002098	ORPHA:60032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002778	ORPHA:60032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0001508	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002015	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002093	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002094	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002105	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002781	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002788	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002789	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0006532	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0010307	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0030828	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0031246	ORPHA:60032	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0001279	ORPHA:60032	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0001945	ORPHA:60032	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002088	ORPHA:60032	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002779	ORPHA:60032	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0002860	ORPHA:60032	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0030842	ORPHA:60032	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60032	Recurrent respiratory papillomatosis		HP:0100750	ORPHA:60032	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000218	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000238	ORPHA:85335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000276	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000280	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000322	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000365	ORPHA:85335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000400	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000587	ORPHA:85335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000718	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0000729	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0001252	ORPHA:85335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0001263	ORPHA:85335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0001264	ORPHA:85335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0001288	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0001317	ORPHA:85335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0002342	ORPHA:85335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0002465	ORPHA:85335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0002514	ORPHA:85335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0002650	ORPHA:85335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0002684	ORPHA:85335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85335	Fried syndrome		HP:0003202	ORPHA:85335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0002110	ORPHA:60033	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0002795	ORPHA:60033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0011947	ORPHA:60033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0031245	ORPHA:60033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0002094	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0002105	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0002783	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0005376	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0030828	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0030830	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0030877	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0100749	ORPHA:60033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0001658	ORPHA:60033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0001945	ORPHA:60033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0002097	ORPHA:60033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0004326	ORPHA:60033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0011949	ORPHA:60033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0100812	ORPHA:60033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60033	Idiopathic bronchiectasis		HP:0001217	ORPHA:60033	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001678	ORPHA:60041	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001709	ORPHA:60041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001622	ORPHA:60041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0030365	ORPHA:60041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0000961	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0000975	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0000980	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001279	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001511	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001562	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001612	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001635	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001643	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001655	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001662	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001698	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001789	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0003546	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0005184	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0008872	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0011706	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0012378	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0012398	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0030830	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0033113	ORPHA:60041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0001706	ORPHA:60041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0002202	ORPHA:60041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0011705	ORPHA:60041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60041	Congenital heart block		HP:0031653	ORPHA:60041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2017	Sternal cleft		HP:0000765	ORPHA:2017	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2017	Sternal cleft		HP:0000766	ORPHA:2017	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2017	Sternal cleft		HP:0010309	ORPHA:2017	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2017	Sternal cleft		HP:0002094	ORPHA:2017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2017	Sternal cleft		HP:0002205	ORPHA:2017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2017	Sternal cleft		HP:0012735	ORPHA:2017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0000160	ORPHA:2016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0000175	ORPHA:2016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0000232	ORPHA:2016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0000293	ORPHA:2016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0000347	ORPHA:2016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0000581	ORPHA:2016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0001608	ORPHA:2016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2016	Cleft palate-lateral synechia syndrome		HP:0010285	ORPHA:2016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0000175	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0000219	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0000286	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0000347	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0000358	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0000463	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0000470	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0001249	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0003196	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0003468	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2015	Cleft palate-short stature-vertebral anomalies syndrome		HP:0004322	ORPHA:2015	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000154	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000256	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000324	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001052	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001161	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001770	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001829	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0006101	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0100026	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0100555	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0100585	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0100761	ORPHA:60040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000238	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000293	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000348	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000965	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001034	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001249	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001252	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001263	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001508	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0002007	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0002119	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0001382	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0007360	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0012639	ORPHA:60040	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000490	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0000648	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0002126	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0002308	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0002637	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0002664	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0005280	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0011675	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60040	Megalencephaly-capillary malformation-polymicrogyria syndrome		HP:0030680	ORPHA:60040	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0000505	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0000654	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0000662	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0001133	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0007722	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0007760	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0030491	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0031528	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0200065	ORPHA:41751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0000551	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0000580	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0000603	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0000618	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0001129	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0001141	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0007814	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0011505	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0030329	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:41751	Bietti crystalline dystrophy		HP:0030528	ORPHA:41751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000047	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000175	ORPHA:2013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000212	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000252	ORPHA:2013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000347	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000400	ORPHA:2013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000411	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000508	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0000767	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0001252	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0001263	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0001800	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0002750	ORPHA:2013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0003202	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0004322	ORPHA:2013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0004428	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0006709	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0009465	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2013	Cleft palate-large ears-small head syndrome		HP:0009882	ORPHA:2013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0000175	ORPHA:2010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0000413	ORPHA:2010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0000506	ORPHA:2010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0003019	ORPHA:2010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0003028	ORPHA:2010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0008368	ORPHA:2010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0008513	ORPHA:2010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0009702	ORPHA:2010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2010	Cleft palate-stapes fixation-oligodontia syndrome		HP:0012225	ORPHA:2010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0001608	ORPHA:99977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0001864	ORPHA:99977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0002017	ORPHA:99977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0002716	ORPHA:99977	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0008872	ORPHA:99977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0011459	ORPHA:99977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0012735	ORPHA:99977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99977	Squamous cell carcinoma of the esophagus		HP:0100749	ORPHA:99977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0000952	ORPHA:99978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0001824	ORPHA:99978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0001945	ORPHA:99978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0002027	ORPHA:99978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0002240	ORPHA:99978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0002716	ORPHA:99978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0004936	ORPHA:99978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0012334	ORPHA:99978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0012378	ORPHA:99978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99978	Perihilar cholangiocarcinoma		HP:0030153	ORPHA:99978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001635	ORPHA:3342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002616	ORPHA:3342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002617	ORPHA:3342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0004942	ORPHA:3342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0005344	ORPHA:3342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0100545	ORPHA:3342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0100585	ORPHA:3342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000023	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000276	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000316	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000400	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000963	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000974	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001363	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002647	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0004415	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001382	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0009099	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0010668	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0012378	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0100541	ORPHA:3342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000256	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000272	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000486	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000545	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000563	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000581	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0000822	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001119	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001166	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001249	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001252	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001263	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001328	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001385	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001582	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001637	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001639	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001644	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001658	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001695	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0001838	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002020	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002021	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002036	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002094	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002098	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002650	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002673	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002812	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002827	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0002878	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0003196	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0004209	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0005743	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0006543	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0007495	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0011302	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0012745	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0012819	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3342	Arterial tortuosity syndrome		HP:0100633	ORPHA:3342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0005616	ORPHA:420179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000098	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000256	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000275	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000300	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000348	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000486	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000494	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000767	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0001319	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002079	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002119	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002162	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002342	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0003100	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0008872	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0011220	ORPHA:420179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000160	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000218	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000307	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000324	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000490	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000543	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000639	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0000739	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0001250	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0001256	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0001357	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002007	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002076	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002131	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002365	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0002650	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0005280	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0006956	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0007766	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0010864	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420179	Malan overgrowth syndrome		HP:0030799	ORPHA:420179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0002982	ORPHA:3344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0002991	ORPHA:3344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0002992	ORPHA:3344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0003103	ORPHA:3344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0003510	ORPHA:3344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0006487	ORPHA:3344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0010502	ORPHA:3344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0001249	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0002650	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0002808	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0002823	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0002980	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0003177	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0003272	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0003312	ORPHA:3344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0000820	ORPHA:3344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0001903	ORPHA:3344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0031095	ORPHA:3344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0006501	ORPHA:3344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3344	Weismann-Netter syndrome		HP:0040071	ORPHA:3344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3346	Tracheal agenesis		HP:0001561	ORPHA:3346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3346	Tracheal agenesis		HP:0001671	ORPHA:3346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3346	Tracheal agenesis		HP:0002093	ORPHA:3346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3346	Tracheal agenesis		HP:0006703	ORPHA:3346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3346	Tracheal agenesis		HP:0100682	ORPHA:3346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0001171	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0002823	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0002983	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0003041	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0005792	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0006101	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0006501	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0040071	ORPHA:2019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0002991	ORPHA:2019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0009811	ORPHA:2019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0009812	ORPHA:2019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0100560	ORPHA:2019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0004322	ORPHA:2019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2019	Femur-fibula-ulna complex		HP:0009828	ORPHA:2019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3347	Mounier-Kühn syndrome		HP:0002086	ORPHA:3347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3347	Mounier-Kühn syndrome		HP:0002090	ORPHA:3347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3347	Mounier-Kühn syndrome		HP:0002205	ORPHA:3347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3347	Mounier-Kühn syndrome		HP:0002777	ORPHA:3347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3347	Mounier-Kühn syndrome		HP:0006538	ORPHA:3347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3347	Mounier-Kühn syndrome		HP:0010776	ORPHA:3347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3347	Mounier-Kühn syndrome		HP:0012387	ORPHA:3347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0001513	ORPHA:99976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0001864	ORPHA:99976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0002017	ORPHA:99976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0002020	ORPHA:99976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0002716	ORPHA:99976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0008872	ORPHA:99976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0011459	ORPHA:99976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0012735	ORPHA:99976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0100580	ORPHA:99976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99976	Adenocarcinoma of the oesophagus and oesophagogastric junction		HP:0100749	ORPHA:99976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0000590	ORPHA:352447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0000508	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0001265	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0001611	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0001618	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0001644	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002015	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002018	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002094	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002719	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002808	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002878	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0003198	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0003200	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0003236	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0003306	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0003388	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0003546	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0003700	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0008443	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0030319	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0040013	ORPHA:352447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0000787	ORPHA:352447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002747	ORPHA:352447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0004396	ORPHA:352447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0000252	ORPHA:352447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0000815	ORPHA:352447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0001249	ORPHA:352447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0001272	ORPHA:352447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0002014	ORPHA:352447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome		HP:0011675	ORPHA:352447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352447	Progressive external ophthalmoplegia-myopathy-emaciation syndrome	NOT	HP:0000651	ORPHA:352447	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002787	ORPHA:3348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0031245	ORPHA:3348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0001945	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002090	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002205	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002777	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002781	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002875	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0005607	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0012387	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0025426	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0032016	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0100593	ORPHA:3348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0001609	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002105	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0006532	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0010307	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0030828	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0031352	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0100633	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0100749	ORPHA:3348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0002093	ORPHA:3348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3348	Tracheobronchopathia osteochondroplastica		HP:0100750	ORPHA:3348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99971	Well-differentiated liposarcoma		HP:0001482	ORPHA:99971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99971	Well-differentiated liposarcoma		HP:0002579	ORPHA:99971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99971	Well-differentiated liposarcoma		HP:0012211	ORPHA:99971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000194	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000252	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000276	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000325	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000331	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000348	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000411	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0000718	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0001263	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0001288	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0001290	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0001999	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0002187	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0002353	ORPHA:85329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0003189	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0003198	ORPHA:85329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0003202	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0004322	ORPHA:85329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85329	X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome		HP:0011968	ORPHA:85329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis		HP:0001974	ORPHA:26137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis		HP:0002315	ORPHA:26137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis		HP:0200036	ORPHA:26137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis		HP:0000509	ORPHA:26137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis		HP:0001880	ORPHA:26137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis		HP:0003193	ORPHA:26137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis	NOT	HP:0002633	ORPHA:26137	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:26137	Juvenile temporal arteritis	NOT	HP:0002637	ORPHA:26137	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0000529	ORPHA:52427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0000662	ORPHA:52427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0008323	ORPHA:52427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0030506	ORPHA:52427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0030825	ORPHA:52427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0000603	ORPHA:52427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0000613	ORPHA:52427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0007675	ORPHA:52427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0007814	ORPHA:52427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0007843	ORPHA:52427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0007987	ORPHA:52427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0007994	ORPHA:52427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0001105	ORPHA:52427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0001142	ORPHA:52427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0007401	ORPHA:52427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0008527	ORPHA:52427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0011505	ORPHA:52427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0031605	ORPHA:52427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52427	Retinitis punctata albescens		HP:0000580	ORPHA:52427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001249	ORPHA:261652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001263	ORPHA:261652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001999	ORPHA:261652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000078	ORPHA:261652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000708	ORPHA:261652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001548	ORPHA:261652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001627	ORPHA:261652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002719	ORPHA:261652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0410263	ORPHA:261652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000023	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000076	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000077	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000179	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000252	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000365	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000729	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000750	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001250	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001270	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001321	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001508	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001520	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002020	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002079	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002119	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002194	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002463	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002500	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0004322	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0006863	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0009909	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0011351	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0011800	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0033127	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0100716	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0200005	ORPHA:261652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000164	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000248	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000519	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000540	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000695	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000826	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0000974	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001182	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001252	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001357	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0001537	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002023	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002171	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261652	Kleefstra syndrome due to a point mutation		HP:0002779	ORPHA:261652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000324	ORPHA:52429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000347	ORPHA:52429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000356	ORPHA:52429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000359	ORPHA:52429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000384	ORPHA:52429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000405	ORPHA:52429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000407	ORPHA:52429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000413	ORPHA:52429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0004467	ORPHA:52429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0008609	ORPHA:52429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0009795	ORPHA:52429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0010628	ORPHA:52429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000175	ORPHA:52429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000365	ORPHA:52429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0000614	ORPHA:52429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52429	Branchiootic syndrome		HP:0100267	ORPHA:52429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0000098	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0000377	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0000391	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0000574	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0000691	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001176	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001182	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001252	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001263	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001284	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001513	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001833	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0001999	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0002342	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0002857	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0007477	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0009928	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0010761	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0010804	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0010864	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0011968	ORPHA:85325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85325	X-linked intellectual disability, Stevenson type		HP:0100540	ORPHA:85325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0000272	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0000316	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0000343	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0000349	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0000455	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0000463	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0001249	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0002003	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0002007	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0004209	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0004322	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85326	X-linked intellectual disability, Stoll type		HP:0005281	ORPHA:85326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0009745	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0030353	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome	NOT	HP:0003564	ORPHA:85327	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0000053	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0000325	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0000718	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0000752	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0000845	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0001260	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0002187	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0003189	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85327	X-linked intellectual disability-acromegaly-hyperactivity syndrome		HP:0007361	ORPHA:85327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0002829	ORPHA:247353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0003565	ORPHA:247353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0025474	ORPHA:247353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0200039	ORPHA:247353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001019	ORPHA:247353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001597	ORPHA:247353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0012531	ORPHA:247353	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001369	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001945	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001974	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0011227	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0012378	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0025252	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0025502	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0100825	ORPHA:247353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0000083	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001513	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001888	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0002901	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0002902	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0002910	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0003073	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0010741	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0100847	ORPHA:247353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0000554	ORPHA:247353	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0001635	ORPHA:247353	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247353	Generalized pustular psoriasis		HP:0100806	ORPHA:247353	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000028	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000048	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000083	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000089	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000110	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000154	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000164	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000179	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000232	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000252	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000272	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000286	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000347	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000369	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000407	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000431	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000506	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000518	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000545	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000581	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000689	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0000821	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0001537	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0001876	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0002342	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0004322	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0006610	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0006709	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0007477	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0008736	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0010864	ORPHA:85321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85321	Deafness-intellectual disability syndrome, Martin-Probst type		HP:0100585	ORPHA:85321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000023	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000028	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000034	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000160	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000286	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000411	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000426	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0000750	ORPHA:85322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0001182	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0001250	ORPHA:85322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0001263	ORPHA:85322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0001276	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0001288	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0001511	ORPHA:85322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0002205	ORPHA:85322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0002510	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0002750	ORPHA:85322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85322	X-linked intellectual disability, Pai type		HP:0010864	ORPHA:85322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0012760	ORPHA:329249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0000842	ORPHA:329249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0001513	ORPHA:329249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0002591	ORPHA:329249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0004322	ORPHA:329249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0000718	ORPHA:329249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0000750	ORPHA:329249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency		HP:0008763	ORPHA:329249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency	NOT	HP:0002910	ORPHA:329249	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency	NOT	HP:0003074	ORPHA:329249	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:329249	Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency	NOT	HP:0003077	ORPHA:329249	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:458798	Spinocerebellar ataxia type 41		HP:0002066	ORPHA:458798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458798	Spinocerebellar ataxia type 41		HP:0002172	ORPHA:458798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458798	Spinocerebellar ataxia type 41		HP:0006855	ORPHA:458798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000028	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000135	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000252	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000278	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000286	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000316	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000400	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000519	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0001249	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0001250	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0001518	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0002191	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0003202	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0009004	ORPHA:85323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0000218	ORPHA:85323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85323	X-linked intellectual disability, Seemanova type		HP:0001627	ORPHA:85323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85324	X-linked intellectual disability, Shrimpton type		HP:0000252	ORPHA:85324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85324	X-linked intellectual disability, Shrimpton type		HP:0000348	ORPHA:85324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85324	X-linked intellectual disability, Shrimpton type		HP:0000486	ORPHA:85324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85324	X-linked intellectual disability, Shrimpton type		HP:0004322	ORPHA:85324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85324	X-linked intellectual disability, Shrimpton type		HP:0010864	ORPHA:85324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000347	ORPHA:3338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000377	ORPHA:3338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000506	ORPHA:3338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001249	ORPHA:3338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001273	ORPHA:3338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0003196	ORPHA:3338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0012745	ORPHA:3338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000028	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000174	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000175	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000260	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000293	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000365	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000470	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001252	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001274	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001545	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001671	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0002251	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0004322	ORPHA:3338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000218	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000252	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000369	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000391	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0000774	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001156	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001250	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001338	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001511	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001600	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001638	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001642	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001643	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0002059	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0002079	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0002119	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0002643	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0007360	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0008872	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0008897	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0030084	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0045075	ORPHA:3338	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001305	ORPHA:3338	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001636	ORPHA:3338	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0001680	ORPHA:3338	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3338	Toriello-Carey syndrome		HP:0009892	ORPHA:3338	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000047	ORPHA:3339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000625	ORPHA:3339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001999	ORPHA:3339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000502	ORPHA:3339	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001140	ORPHA:3339	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001274	ORPHA:3339	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001331	ORPHA:3339	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0007440	ORPHA:3339	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0008065	ORPHA:3339	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0012639	ORPHA:3339	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000069	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000256	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000286	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000365	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000463	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000486	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000506	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000520	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000581	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000598	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001156	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001252	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001508	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001510	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001561	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0001626	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0002251	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0003196	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0004279	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0008749	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0011968	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0012745	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0030680	ORPHA:3339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000014	ORPHA:3339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000036	ORPHA:3339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3339	Oculoectodermal syndrome		HP:0000039	ORPHA:3339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0008751	ORPHA:2004	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0000961	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0001601	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0001608	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0001615	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0002094	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0002205	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0002835	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0010307	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0012735	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0030842	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0031162	ORPHA:2004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2004	Laryngotracheoesophageal cleft		HP:0002643	ORPHA:2004	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0000324	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0000457	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0001251	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0002209	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0002435	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0100337	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0002827	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0005273	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0008625	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0009804	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0012033	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0100335	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2003	Cleft lip/palate-deafness-sacral lipoma syndrome		HP:0100559	ORPHA:2003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0000316	ORPHA:2001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0000347	ORPHA:2001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0000470	ORPHA:2001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0100337	ORPHA:2001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0005469	ORPHA:2001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0012368	ORPHA:2001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0030680	ORPHA:2001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0000582	ORPHA:2001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0004209	ORPHA:2001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0004383	ORPHA:2001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0001643	ORPHA:2001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0001679	ORPHA:2001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0002566	ORPHA:2001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0010297	ORPHA:2001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2001	Cleft lip/palate-intestinal malrotation-cardiopathy syndrome		HP:0011304	ORPHA:2001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0000238	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0000256	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0000737	ORPHA:99966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0000741	ORPHA:99966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0001250	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0001251	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0001324	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0001376	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0002017	ORPHA:99966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0002076	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0002514	ORPHA:99966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0004372	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0004374	ORPHA:99966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0006824	ORPHA:99966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0100021	ORPHA:99966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99966	Atypical teratoid rhabdoid tumor		HP:0100836	ORPHA:99966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99967	Myxoid/round cell liposarcoma		HP:0001482	ORPHA:99967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99967	Myxoid/round cell liposarcoma		HP:0002027	ORPHA:99967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99967	Myxoid/round cell liposarcoma		HP:0002579	ORPHA:99967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99969	Pleomorphic liposarcoma		HP:0012034	ORPHA:99969	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99969	Pleomorphic liposarcoma		HP:0001482	ORPHA:99969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0003347	ORPHA:35078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0005354	ORPHA:35078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0005403	ORPHA:35078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0031381	ORPHA:35078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0001888	ORPHA:35078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0002028	ORPHA:35078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0002205	ORPHA:35078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0005390	ORPHA:35078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0009098	ORPHA:35078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0040219	ORPHA:35078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0000371	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0001531	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0002850	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0004315	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0004429	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0004798	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0006532	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0010976	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0011837	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0200039	ORPHA:35078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0000143	ORPHA:35078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0000953	ORPHA:35078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0000988	ORPHA:35078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0001433	ORPHA:35078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35078	T-B+ severe combined immunodeficiency due to JAK3 deficiency		HP:0001999	ORPHA:35078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000506	ORPHA:572333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000508	ORPHA:572333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000537	ORPHA:572333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000581	ORPHA:572333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000322	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000369	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000431	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000539	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000633	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000646	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0007656	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0011481	ORPHA:572333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000013	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000144	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000147	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000486	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000574	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000656	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000815	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000869	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000876	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0002553	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0007732	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0007835	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0008209	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0008214	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0008222	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0008232	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0008233	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0010464	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0010748	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0011969	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0025572	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0032514	ORPHA:572333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572333	Blepharophimosis-ptosis-epicanthus inversus syndrome plus		HP:0000639	ORPHA:572333	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000369	ORPHA:2008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001171	ORPHA:2008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001249	ORPHA:2008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0008872	ORPHA:2008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000028	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000047	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000175	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000204	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000316	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000348	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000431	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000527	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001511	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001839	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0002120	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0005916	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0008736	ORPHA:2008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000520	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0000836	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001250	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001252	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001276	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001373	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001522	ORPHA:2008	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001629	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001631	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001636	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001660	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001680	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001718	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001770	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001822	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0001829	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0002023	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0006101	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0100490	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2008	Acrocardiofacial syndrome		HP:0100589	ORPHA:2008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002460	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002515	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003236	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003307	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003458	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003557	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003701	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003805	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0012083	ORPHA:52430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0000925	ORPHA:52430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002145	ORPHA:52430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002797	ORPHA:52430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003155	ORPHA:52430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0004322	ORPHA:52430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0012444	ORPHA:52430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0030838	ORPHA:52430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0000518	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0001249	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0001293	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0001397	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0001635	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0001638	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002300	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002380	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002381	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002442	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002450	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002463	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002493	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002659	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002683	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002839	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003390	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003444	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003445	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0003700	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0004347	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0004490	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0007002	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0007354	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0011314	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0012548	ORPHA:52430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		HP:0002756	ORPHA:52430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2007	Alar cartilages hypoplasia-coloboma-telecanthus syndrome		HP:0000316	ORPHA:2007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2007	Alar cartilages hypoplasia-coloboma-telecanthus syndrome		HP:0000430	ORPHA:2007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2007	Alar cartilages hypoplasia-coloboma-telecanthus syndrome		HP:0000431	ORPHA:2007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2007	Alar cartilages hypoplasia-coloboma-telecanthus syndrome		HP:0000444	ORPHA:2007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2007	Alar cartilages hypoplasia-coloboma-telecanthus syndrome		HP:0000506	ORPHA:2007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2007	Alar cartilages hypoplasia-coloboma-telecanthus syndrome		HP:0003191	ORPHA:2007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2007	Alar cartilages hypoplasia-coloboma-telecanthus syndrome		HP:0100335	ORPHA:2007	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0003457	ORPHA:99965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0003484	ORPHA:99965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0008954	ORPHA:99965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0030237	ORPHA:99965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0001337	ORPHA:99965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0002380	ORPHA:99965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0003444	ORPHA:99965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0006827	ORPHA:99965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0012531	ORPHA:99965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0031372	ORPHA:99965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0001880	ORPHA:99965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome		HP:0010702	ORPHA:99965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome	NOT	HP:0003474	ORPHA:99965	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99965	O'Sullivan-McLeod syndrome	NOT	HP:0040272	ORPHA:99965	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0000117	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0001510	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002049	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002909	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003076	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003126	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003149	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003646	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0004910	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0004918	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0032943	ORPHA:3337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0001324	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0001824	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002148	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002653	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002659	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002749	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002900	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003081	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003234	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003537	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0004912	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0012606	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0012622	ORPHA:3337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0001944	ORPHA:3337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002150	ORPHA:3337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0003774	ORPHA:3337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0001943	ORPHA:3337	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3337	Primary Fanconi renotubular syndrome		HP:0002206	ORPHA:3337	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0000252	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0000308	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0000486	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001252	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001257	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001274	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001320	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001339	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0002069	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0002079	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0002198	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0002365	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0025101	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0034051	ORPHA:171680	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0000609	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0000639	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001302	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001338	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0002126	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0006989	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0007359	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0012469	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0012650	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0025517	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0031882	ORPHA:171680	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0002251	ORPHA:171680	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0001263	ORPHA:171680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0002119	ORPHA:171680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171680	Lissencephaly due to TUBA1A mutation		HP:0025102	ORPHA:171680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0000077	ORPHA:53721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0000763	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0000925	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0001014	ORPHA:53721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0001052	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0001347	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0001635	ORPHA:53721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0002143	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0002385	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0002390	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0002653	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0002751	ORPHA:53721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0002829	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0002839	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0006773	ORPHA:53721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0012378	ORPHA:53721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0100026	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0100758	ORPHA:53721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0100761	ORPHA:53721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53721	Spinal arteriovenous metameric syndrome		HP:0100764	ORPHA:53721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0000280	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0001249	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0001250	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0001263	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0001290	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0002828	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0005876	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85319	X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome		HP:0008872	ORPHA:85319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000175	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000303	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000316	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000322	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000336	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000411	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000664	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0000998	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0001250	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0001251	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0001272	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0001288	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0001324	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0002342	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0002344	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0002650	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0002808	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0004313	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0005487	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0007598	ORPHA:85317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85317	X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome		HP:0009830	ORPHA:85317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0002697	ORPHA:60015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0000932	ORPHA:60015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0002013	ORPHA:60015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0002315	ORPHA:60015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0012721	ORPHA:60015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0100809	ORPHA:60015	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0000175	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0000894	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0001249	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0001250	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0001363	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0002085	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0002475	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0002762	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0007385	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0008497	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0011304	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0012480	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0040197	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60015	Enlarged parietal foramina		HP:0410030	ORPHA:60015	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0002172	ORPHA:171684	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0034773	ORPHA:171684	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0002141	ORPHA:171684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0002321	ORPHA:171684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0007670	ORPHA:171684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:6001104	ORPHA:171684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0000739	ORPHA:171684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0002354	ORPHA:171684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:0031987	ORPHA:171684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy		HP:5200273	ORPHA:171684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171684	Idiopathic bilateral vestibulopathy	NOT	HP:0000407	ORPHA:171684	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000023	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000028	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000076	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000126	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000218	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000238	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000252	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000286	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000343	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000407	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000414	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000431	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000486	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000490	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000518	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000568	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000612	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000716	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000717	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0000739	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001161	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001249	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001250	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001252	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001263	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001274	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001508	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001511	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001643	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001671	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001762	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001770	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001773	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001829	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0002007	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0002360	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0002650	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0004209	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0004322	ORPHA:250989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0001382	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0007018	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0008499	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0010059	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0010296	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0011304	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0011611	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250989	1q21.1 microdeletion syndrome		HP:0100753	ORPHA:250989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000028	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000078	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000175	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000176	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000271	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000280	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000430	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000455	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000486	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000490	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000525	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000582	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000601	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000708	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000776	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0000815	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001249	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001250	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001263	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001319	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001360	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001510	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0004322	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001762	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0001792	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0002011	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0002007	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0002089	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0005280	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0011344	ORPHA:250999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0011447	ORPHA:250999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250999	1q41q42 microdeletion syndrome		HP:0012471	ORPHA:250999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0000083	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0000123	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0000407	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0001250	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0001336	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0001350	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0001873	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0002470	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0009127	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome		HP:0009798	ORPHA:3327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3327	Thyrocerebrorenal syndrome	NOT	HP:0001249	ORPHA:3327	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0000396	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0001156	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0001162	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0001171	ORPHA:3329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0001177	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0001376	ORPHA:3329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0001539	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0002823	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0002980	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0002991	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0003038	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0003097	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0005772	ORPHA:3329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0006101	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0006443	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0006495	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0009756	ORPHA:3329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3329	Tibial aplasia-ectrodactyly syndrome		HP:0100257	ORPHA:3329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85320	X-linked intellectual disability-macrocephaly-macroorchidism syndrome		HP:0000053	ORPHA:85320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85320	X-linked intellectual disability-macrocephaly-macroorchidism syndrome		HP:0000256	ORPHA:85320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85320	X-linked intellectual disability-macrocephaly-macroorchidism syndrome		HP:0002342	ORPHA:85320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000028	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000047	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000238	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000256	ORPHA:250994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000316	ORPHA:250994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000486	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000501	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000518	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000717	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0000738	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001249	ORPHA:250994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001250	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001252	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001263	ORPHA:250994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001276	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001385	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001508	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001636	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0001762	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0002007	ORPHA:250994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0002020	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0002804	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0002827	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0007018	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250994	1q21.1 microduplication syndrome		HP:0100753	ORPHA:250994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000077	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000085	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000119	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000151	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000175	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000337	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000347	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000348	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000358	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000407	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0000891	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0001181	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0001636	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0001671	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0001873	ORPHA:3320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0001928	ORPHA:3320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0002650	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0002673	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0002827	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0002949	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0002970	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0002990	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0002999	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0003974	ORPHA:3320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0004209	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0004717	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0006101	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0006495	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0006498	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0006507	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0007413	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0009829	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0011304	ORPHA:3320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3320	Thrombocytopenia-absent radius syndrome		HP:0100694	ORPHA:3320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001760	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001288	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0002522	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0004336	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0007010	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0007230	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0007340	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0008959	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0009053	ORPHA:99956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000501	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001605	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001618	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001761	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0002650	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0002751	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0002936	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0008994	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0012046	ORPHA:99956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000183	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000407	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000508	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000518	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000557	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000648	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0000729	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001026	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001087	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001270	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001328	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001337	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0001763	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0002093	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0002540	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0002792	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0003401	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0008997	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0012473	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0030051	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0030237	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99956	Charcot-Marie-Tooth disease type 4B2		HP:0030319	ORPHA:99956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0000252	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001249	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001251	ORPHA:3322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001263	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001265	ORPHA:3322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001276	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001321	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001508	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001511	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001873	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001881	ORPHA:3322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001903	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0001928	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002119	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002120	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002209	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002216	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002514	ORPHA:3322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002664	ORPHA:3322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002721	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0002745	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0004322	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0004334	ORPHA:3322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0005528	ORPHA:3322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0007392	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0007440	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0008404	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3322	Hoyeraal-Hreidarsson syndrome		HP:0011358	ORPHA:3322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002099	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002205	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002718	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002719	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002783	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002788	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002960	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0032169	ORPHA:183675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0000010	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0000403	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0001047	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0001369	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002090	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002110	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002720	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002725	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002829	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002850	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0003193	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0003326	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0004315	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0005231	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0006532	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0011109	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0011110	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0012378	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0012387	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0020096	ORPHA:183675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0000031	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0000819	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0000988	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0001082	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0001370	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002608	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0002665	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0003765	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0005353	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0006562	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0012476	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0030151	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0030998	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0032262	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0032275	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0100324	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0100523	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0100806	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:183675	Recurrent infections associated with rare immunoglobulin isotypes deficiency		HP:0500093	ORPHA:183675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0001907	ORPHA:3325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0001973	ORPHA:3325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0100724	ORPHA:3325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0002625	ORPHA:3325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0003144	ORPHA:3325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0004420	ORPHA:3325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0004936	ORPHA:3325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0001297	ORPHA:3325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0001658	ORPHA:3325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0002204	ORPHA:3325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0002637	ORPHA:3325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0005521	ORPHA:3325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0012649	ORPHA:3325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0030248	ORPHA:3325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3325	Classic heparin-induced thrombocytopenia		HP:0040231	ORPHA:3325	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0001284	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0001760	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0002495	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0002936	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0003409	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0003431	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0003477	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0007108	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0007230	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0009053	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0011096	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0012078	ORPHA:99953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0001155	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0001761	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0001762	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0001288	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0003693	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0003701	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0007210	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0008959	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0009129	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0010830	ORPHA:99953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0002141	ORPHA:99953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0002505	ORPHA:99953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0002650	ORPHA:99953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0007328	ORPHA:99953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99953	Charcot-Marie-Tooth disease type 4G		HP:0008081	ORPHA:99953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0003431	ORPHA:99950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0007078	ORPHA:99950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0007108	ORPHA:99950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0009053	ORPHA:99950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0000407	ORPHA:99950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0001270	ORPHA:99950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0001760	ORPHA:99950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0002317	ORPHA:99950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0002460	ORPHA:99950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0007210	ORPHA:99950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0001171	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0001761	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0001765	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0002174	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0002540	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0002751	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0002936	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0003474	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0003701	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0008959	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0009129	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99950	Charcot-Marie-Tooth disease type 4D		HP:0032649	ORPHA:99950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0002912	ORPHA:289504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0003215	ORPHA:289504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0012120	ORPHA:289504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0040145	ORPHA:289504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001250	ORPHA:289504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0000252	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0000708	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0000750	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001263	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001298	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001332	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001508	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001941	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001943	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001944	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0001993	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0002013	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0002076	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0002254	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0002354	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0002384	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0002910	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0008936	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0011169	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0031064	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289504	Combined malonic and methylmalonic acidemia		HP:0040288	ORPHA:289504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002091	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002094	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0005317	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0012378	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0030874	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0031246	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0032094	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0100749	ORPHA:60025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0000961	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0001708	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0001824	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002093	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002105	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002107	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002110	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002113	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002240	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002789	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002875	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0003473	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0012398	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0012418	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0025178	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0030879	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0031944	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0100759	ORPHA:60025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0000144	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0000790	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0001945	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002206	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0002878	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0004241	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0004382	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0004724	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0004963	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0008703	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0010766	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0011947	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0012215	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0012387	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis		HP:0025179	ORPHA:60025	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis	NOT	HP:0004363	ORPHA:60025	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:60025	Pulmonary alveolar microlithiasis	NOT	HP:0100529	ORPHA:60025	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0002729	ORPHA:60026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0012735	ORPHA:60026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0025392	ORPHA:60026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0030150	ORPHA:60026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0100721	ORPHA:60026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0002094	ORPHA:60026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0025179	ORPHA:60026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0100749	ORPHA:60026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0002721	ORPHA:60026	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:60026	Pulmonary nodular lymphoid hyperplasia		HP:0030057	ORPHA:60026	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0001300	ORPHA:171695	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0007256	ORPHA:171695	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0000011	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0000338	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0000514	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0001257	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0001332	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0001336	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0001347	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0001762	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002015	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002063	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002067	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002080	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002172	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002360	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002362	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0002367	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0003487	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0011960	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0012332	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0031435	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0100543	ORPHA:171695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0000726	ORPHA:171695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171695	Parkinsonian-pyramidal syndrome		HP:0100315	ORPHA:171695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0000252	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0001317	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0002060	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0002119	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0002472	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0002538	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0009879	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0012444	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329228	Microcephalic primordial dwarfism due to ZNF335 deficiency		HP:0012757	ORPHA:329228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0000003	ORPHA:3316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0000175	ORPHA:3316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0000204	ORPHA:3316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0001562	ORPHA:3316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0008678	ORPHA:3316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0030680	ORPHA:3316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0000268	ORPHA:3316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0000316	ORPHA:3316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0000348	ORPHA:3316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0000494	ORPHA:3316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3316	Thomas syndrome		HP:0004383	ORPHA:3316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001643	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001763	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0002617	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0002647	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0004942	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0005116	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0005294	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0100718	ORPHA:60030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000098	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000175	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000193	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000202	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000272	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000316	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000347	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000592	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000964	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000987	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001065	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001166	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001363	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001382	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001762	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0002099	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0002650	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0100490	ORPHA:60030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000545	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000767	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000768	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000963	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0000978	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001373	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001653	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001695	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001892	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0002108	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0001382	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:60030	Loeys-Dietz syndrome		HP:0410151	ORPHA:60030	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0001892	ORPHA:3318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0002076	ORPHA:3318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0001658	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0001872	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0001894	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0003010	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0003401	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0004420	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0004936	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0005513	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0005561	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0011875	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0012378	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0031388	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0100576	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0100659	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0100749	ORPHA:3318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0001744	ORPHA:3318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0002315	ORPHA:3318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0002321	ORPHA:3318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0100785	ORPHA:3318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0000505	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0000978	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0001974	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0002326	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0002488	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0002863	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0011974	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0030243	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3318	Essential thrombocythemia		HP:0032147	ORPHA:3318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0000280	ORPHA:3319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0000470	ORPHA:3319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0000995	ORPHA:3319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0001671	ORPHA:3319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0001873	ORPHA:3319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0001903	ORPHA:3319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0002650	ORPHA:3319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0003312	ORPHA:3319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0004322	ORPHA:3319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0004331	ORPHA:3319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3319	Congenital amegakaryocytic thrombocytopenia		HP:0011902	ORPHA:3319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000750	ORPHA:329224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001249	ORPHA:329224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001263	ORPHA:329224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001999	ORPHA:329224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000028	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000316	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000369	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000411	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000414	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000494	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000527	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001250	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001488	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001508	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002019	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002553	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0008947	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0012443	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0012523	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0025160	ORPHA:329224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000023	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000154	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000219	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000252	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000294	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000319	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000400	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000589	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000664	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000699	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000729	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000767	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0000954	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001195	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001238	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001260	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001272	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001321	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001344	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001537	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001629	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001631	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001643	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001647	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001655	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0001763	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002020	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002317	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002389	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002650	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002714	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0002951	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0004209	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0005421	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0006610	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0010821	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0011304	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0012210	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329224	Schuurs-Hoeijmakers syndrome		HP:0040288	ORPHA:329224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000407	ORPHA:250984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0002656	ORPHA:250984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0011003	ORPHA:250984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0012368	ORPHA:250984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000272	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000347	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000518	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000545	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0002829	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0003301	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0004327	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0001382	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0005930	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0007773	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0011800	ORPHA:250984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000218	ORPHA:250984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000541	ORPHA:250984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000926	ORPHA:250984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0002650	ORPHA:250984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0002655	ORPHA:250984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0006429	ORPHA:250984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0007992	ORPHA:250984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250984	Autosomal recessive Stickler syndrome		HP:0000175	ORPHA:250984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0000762	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001760	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001761	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0002460	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0002936	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0003457	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0003693	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0007010	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0007015	ORPHA:99948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001270	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001284	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001604	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001609	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001765	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0001776	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0002317	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0002540	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0003387	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0006064	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0006248	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0006858	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0006886	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0006937	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0007267	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0007328	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0009072	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0009473	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0012391	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0030237	ORPHA:99948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0002091	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0002359	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0002650	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0003547	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0003731	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0007108	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0008443	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0008935	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0009109	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0012078	ORPHA:99948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99948	Charcot-Marie-Tooth disease type 4A		HP:0030319	ORPHA:99948	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35093	Non-syndromic sagittal craniosynostosis		HP:0000268	ORPHA:35093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35093	Non-syndromic sagittal craniosynostosis		HP:0000269	ORPHA:35093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35093	Non-syndromic sagittal craniosynostosis		HP:0002007	ORPHA:35093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35093	Non-syndromic sagittal craniosynostosis		HP:0002516	ORPHA:35093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001760	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001288	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0003380	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0003431	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0003444	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0004302	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0007108	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0007141	ORPHA:99949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001284	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001308	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001761	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001765	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002066	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002359	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002460	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002650	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0003326	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0003394	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0003693	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0006886	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0008443	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0009027	ORPHA:99949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0000183	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0000407	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0000486	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0000587	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0000639	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0000651	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001260	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001272	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001385	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001508	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001604	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0001763	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002093	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002307	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002346	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002403	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002540	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0002791	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0007209	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0007328	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0007695	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0009916	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0010871	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0012473	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0030319	ORPHA:99949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0000648	ORPHA:99949	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0007994	ORPHA:99949	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0008081	ORPHA:99949	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99949	Charcot-Marie-Tooth disease type 4C		HP:0100661	ORPHA:99949	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0000762	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0001288	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0002460	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0002936	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0003202	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0003701	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0009130	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0011096	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0011675	ORPHA:99944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99944	Autosomal dominant Charcot-Marie-Tooth disease type 2K		HP:0001270	ORPHA:99944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000316	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000347	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000363	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000486	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000490	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000494	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000545	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000646	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000750	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001263	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000444	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0030434	ORPHA:3310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000010	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000028	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000110	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000126	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000175	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000193	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000218	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000238	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000239	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000286	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000414	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000470	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000532	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000577	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000639	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000678	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000682	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000789	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000798	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000882	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000921	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000952	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000960	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001250	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001290	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001302	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001305	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001328	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001369	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001373	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001511	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001528	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001633	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001671	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001701	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001762	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0002126	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0002143	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0002714	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0002725	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0004209	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0005562	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0005912	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0006710	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0007598	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0009099	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0011044	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0011467	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0012378	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0030031	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0030880	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0040262	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0100614	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0200055	ORPHA:3310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000054	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000085	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000256	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000322	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000705	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000719	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000729	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0000752	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001339	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001537	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001651	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0001655	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0002089	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0002092	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0011646	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3310	Tetrasomy 9p syndrome		HP:0011968	ORPHA:3310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0003281	ORPHA:139507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0001395	ORPHA:139507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0002614	ORPHA:139507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0006562	ORPHA:139507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0012115	ORPHA:139507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0012463	ORPHA:139507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0012465	ORPHA:139507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0000078	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0000819	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0001397	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0001402	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0001413	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0001627	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0001635	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0002240	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0003118	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0011732	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0011772	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0012090	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0012852	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0031035	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0100510	ORPHA:139507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0000939	ORPHA:139507	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0002586	ORPHA:139507	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139507	Dietary iron overload disease		HP:0011459	ORPHA:139507	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0001760	ORPHA:99947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003390	ORPHA:99947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003438	ORPHA:99947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003444	ORPHA:99947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003474	ORPHA:99947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0009027	ORPHA:99947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0001155	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0001761	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002359	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002378	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002495	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002522	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002601	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002936	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003394	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003551	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0006460	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0007010	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0007328	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0009046	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0009053	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0010829	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0025238	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0030237	ORPHA:99947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0001371	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0001605	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0001609	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0001618	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002143	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002174	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003376	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003401	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003487	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0003731	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0006844	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0006915	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0008944	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0012452	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0012513	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0031108	ORPHA:99947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0000238	ORPHA:99947	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0000407	ORPHA:99947	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0000648	ORPHA:99947	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0000662	ORPHA:99947	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99947	Autosomal dominant Charcot-Marie-Tooth disease type 2A2		HP:0002650	ORPHA:99947	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0001171	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0001177	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0001199	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0002991	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0006433	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0004322	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0005613	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0006495	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0006507	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0009601	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0009813	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0030680	ORPHA:3312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0000356	ORPHA:3312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0000365	ORPHA:3312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0000855	ORPHA:3312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0002257	ORPHA:3312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3312	Thalidomide embryopathy		HP:0009892	ORPHA:3312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0001315	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0001762	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0003376	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0003444	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0003445	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0003477	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0007289	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0007328	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0007340	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0008944	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0009129	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99940	Autosomal dominant Charcot-Marie-Tooth disease type 2F		HP:0010829	ORPHA:99940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3314	Thiemann disease, familial form		HP:0000944	ORPHA:3314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3314	Thiemann disease, familial form		HP:0001156	ORPHA:3314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3314	Thiemann disease, familial form		HP:0001376	ORPHA:3314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3314	Thiemann disease, familial form		HP:0005930	ORPHA:3314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3314	Thiemann disease, familial form		HP:0010885	ORPHA:3314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0000248	ORPHA:35099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0000316	ORPHA:35099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0000337	ORPHA:35099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0000365	ORPHA:35099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0000520	ORPHA:35099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0001156	ORPHA:35099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0001249	ORPHA:35099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0002516	ORPHA:35099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0009701	ORPHA:35099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0009891	ORPHA:35099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35099	Non-syndromic bicoronal craniosynostosis		HP:0011800	ORPHA:35099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0000126	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0000175	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0000252	ORPHA:3305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0000322	ORPHA:3305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0000347	ORPHA:3305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0000384	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0000444	ORPHA:3305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0001511	ORPHA:3305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0002308	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0002916	ORPHA:3305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0006433	ORPHA:3305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0004422	ORPHA:3305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0006703	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0008056	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0008678	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0010515	ORPHA:3305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3305	Tetraploidy syndrome		HP:0100720	ORPHA:3305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0000965	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0000967	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0000979	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0001324	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0001945	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0002633	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0012224	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0100721	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0100778	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0200042	ORPHA:91138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0000083	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0000093	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0000790	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0001369	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0001392	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0001744	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0002027	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0002240	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0002829	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0003326	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0005244	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0006562	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0007141	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0009830	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0009831	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0100758	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0100820	ORPHA:91138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0001097	ORPHA:91138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91138	Cryoglobulinemic vasculitis		HP:0002239	ORPHA:91138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0000063	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0000154	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0000219	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0000248	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0000369	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0001250	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0007875	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0008665	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0010864	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250977	AICA-ribosiduria		HP:0011220	ORPHA:250977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0001513	ORPHA:71528	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0009126	ORPHA:71528	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0002591	ORPHA:71528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0001010	ORPHA:71528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0001396	ORPHA:71528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0002297	ORPHA:71528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0008915	ORPHA:71528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0011734	ORPHA:71528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0000823	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0000824	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0000842	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0000956	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0001508	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0001510	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0002173	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0002750	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0008213	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71528	Obesity due to prohormone convertase I deficiency		HP:0008245	ORPHA:71528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0001513	ORPHA:71529	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0009126	ORPHA:71529	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0002591	ORPHA:71529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0005616	ORPHA:71529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0008915	ORPHA:71529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0000822	ORPHA:71529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0000842	ORPHA:71529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0000956	ORPHA:71529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0002155	ORPHA:71529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71529	Obesity due to melanocortin 4 receptor deficiency		HP:0005978	ORPHA:71529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000729	ORPHA:3306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001290	ORPHA:3306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001382	ORPHA:3306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0002307	ORPHA:3306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000733	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000752	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001250	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0006863	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0010529	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0011352	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0011968	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0012169	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0012758	ORPHA:3306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000135	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000218	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000248	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000252	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000286	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000322	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000358	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000455	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000486	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000490	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000494	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000664	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000718	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001156	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001510	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001999	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0004209	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0004691	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0012443	ORPHA:3306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000028	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000122	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000133	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0000826	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001629	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001636	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0001762	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome		HP:0100790	ORPHA:3306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3306	Inverted duplicated chromosome 15 syndrome	NOT	HP:0002007	ORPHA:3306	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000160	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000233	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000252	ORPHA:3307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000271	ORPHA:3307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000286	ORPHA:3307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000324	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000343	ORPHA:3307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000358	ORPHA:3307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0000494	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0001176	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0001249	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0001250	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0001279	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0001288	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0002269	ORPHA:3307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0002571	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0002650	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3307	Tetrasomy 18p syndrome		HP:0003196	ORPHA:3307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0005550	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0006562	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0006824	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0011024	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0032335	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000979	ORPHA:91139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001871	ORPHA:91139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0410135	ORPHA:91139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001955	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0003496	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0006121	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0007067	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0007141	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0009830	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0011355	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0012378	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0030880	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0031047	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0032018	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0033260	ORPHA:91139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000077	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000083	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000093	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000793	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000822	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001369	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001824	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002633	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002829	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002907	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0003401	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0005508	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0006775	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0010833	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0011276	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0012191	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0012574	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0032290	ORPHA:91139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000100	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0000123	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001250	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001297	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001627	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001635	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001658	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0001701	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002011	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002027	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002088	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002239	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002315	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002344	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0002923	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0004302	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91139	Simple cryoglobulinemia		HP:0004431	ORPHA:91139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001250	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001263	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001319	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001321	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001635	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001845	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0002092	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0003196	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0006931	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0011800	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0012368	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0100807	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000316	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000343	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000369	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000431	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000470	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000582	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001508	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001762	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0002098	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0002205	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0004209	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0004467	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0005989	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0008897	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0010109	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0030148	ORPHA:3309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000218	ORPHA:3309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000260	ORPHA:3309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000286	ORPHA:3309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0001612	ORPHA:3309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0002089	ORPHA:3309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0007483	ORPHA:3309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0010318	ORPHA:3309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000238	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000256	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000280	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000293	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000347	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000358	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000463	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000767	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3309	Tetrasomy 5p syndrome		HP:0000961	ORPHA:3309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0000609	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0000707	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0001250	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0001265	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0001319	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0001344	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0002126	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0011344	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0030048	ORPHA:250972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0001274	ORPHA:250972	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0002069	ORPHA:250972	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0002365	ORPHA:250972	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0006989	ORPHA:250972	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250972	Polymicrogyria with optic nerve hypoplasia		HP:0012469	ORPHA:250972	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0001513	ORPHA:71526	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0009126	ORPHA:71526	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0002591	ORPHA:71526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0001010	ORPHA:71526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0001396	ORPHA:71526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0002297	ORPHA:71526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0008915	ORPHA:71526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0011734	ORPHA:71526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0000823	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0000824	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0000842	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0000956	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0001508	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0001510	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0002173	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0002750	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0008213	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71526	Obesity due to pro-opiomelanocortin deficiency		HP:0008245	ORPHA:71526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0002317	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0002495	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0003392	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0003393	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0003426	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0003427	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0003435	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0003484	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0003693	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0007178	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0009053	ORPHA:139536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0001347	ORPHA:139536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0001761	ORPHA:139536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0001765	ORPHA:139536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0008081	ORPHA:139536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139536	Distal hereditary motor neuropathy type 5		HP:0040131	ORPHA:139536	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0001252	ORPHA:91130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0001639	ORPHA:91130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0001942	ORPHA:91130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0002151	ORPHA:91130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0003128	ORPHA:91130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0012103	ORPHA:91130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0000961	ORPHA:91130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0001508	ORPHA:91130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0003198	ORPHA:91130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0009805	ORPHA:91130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91130	Cardiomyopathy-hypotonia-lactic acidosis syndrome		HP:0002098	ORPHA:91130	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91132	Ichthyosis-hypotrichosis syndrome		HP:0008064	ORPHA:91132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91132	Ichthyosis-hypotrichosis syndrome		HP:0008070	ORPHA:91132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0001644	ORPHA:91131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0003642	ORPHA:91131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0012379	ORPHA:91131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0031319	ORPHA:91131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0001250	ORPHA:91131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0001508	ORPHA:91131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0001635	ORPHA:91131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0002910	ORPHA:91131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0008064	ORPHA:91131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0011342	ORPHA:91131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0031329	ORPHA:91131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0000253	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0000486	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0000505	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0000729	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0000817	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0001249	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0001270	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0001344	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0002069	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0002521	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0003323	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0004322	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0006829	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0007359	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0008947	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0010841	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0010845	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0011675	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0012469	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0025335	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91131	DK1-CDG		HP:0031936	ORPHA:91131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0009924	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000003	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000028	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000046	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000148	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000160	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000293	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000347	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000482	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000518	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000568	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000612	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000648	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000772	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000921	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0001274	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0001600	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0001671	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0002023	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0002101	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0002777	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0006709	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0008736	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0009812	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0010494	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0100335	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0100569	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0100842	ORPHA:3301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000202	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0000238	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0001561	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0003057	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0006703	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0008551	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3301	Tetraamelia-multiple malformations syndrome		HP:0009103	ORPHA:3301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0000028	ORPHA:3303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0000233	ORPHA:3303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0000268	ORPHA:3303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0000337	ORPHA:3303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0000520	ORPHA:3303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0001156	ORPHA:3303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0001511	ORPHA:3303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0001636	ORPHA:3303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0004209	ORPHA:3303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0004467	ORPHA:3303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0005105	ORPHA:3303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3303	Tetralogy of Fallot		HP:0009891	ORPHA:3303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0000973	ORPHA:91135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0001582	ORPHA:91135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0001928	ORPHA:91135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0200034	ORPHA:91135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0001102	ORPHA:91135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0001892	ORPHA:91135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0002621	ORPHA:91135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91135	Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency		HP:0004944	ORPHA:91135	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0002073	ORPHA:352403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0000750	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001256	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001260	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001263	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001272	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001310	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001347	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001350	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0002075	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0002078	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0007240	ORPHA:352403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0000486	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0000639	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0000641	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0000651	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0000666	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0001257	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0002080	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352403	Spectrin-associated autosomal recessive cerebellar ataxia		HP:0008003	ORPHA:352403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000411	ORPHA:3304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0001525	ORPHA:3304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0002187	ORPHA:3304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000028	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000218	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000252	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000347	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000400	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000494	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000954	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0001631	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0001636	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0001642	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0001719	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0004691	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0011335	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0011344	ORPHA:3304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000219	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000316	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000348	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000403	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000431	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000486	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0000961	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0001276	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0001643	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0002179	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0002623	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0005278	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0005301	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0007687	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0100759	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3304	Fallot complex-intellectual disability-growth delay syndrome		HP:0100760	ORPHA:3304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000280	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000316	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000319	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000322	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000358	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000445	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000527	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000563	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000574	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000582	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000664	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000750	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001249	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001373	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001376	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001513	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001762	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001773	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001840	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001999	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0002487	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0002857	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0003077	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0003763	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0004209	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0004322	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0006316	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0009907	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0011098	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0011822	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0200055	ORPHA:289522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000175	ORPHA:289522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000252	ORPHA:289522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000365	ORPHA:289522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0000470	ORPHA:289522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0001290	ORPHA:289522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0002650	ORPHA:289522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome		HP:0006951	ORPHA:289522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289522	Microtriplication 11q24.1 syndrome	NOT	HP:0001250	ORPHA:289522	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0000062	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0000252	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0000316	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0000612	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0000648	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0001155	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0001276	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0001360	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0001671	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0002023	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0002084	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0002323	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0003312	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0004322	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0005916	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0007370	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0008056	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0008207	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0008678	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0009601	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0100543	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1590	Distal deletion 13q syndrome		HP:0100589	ORPHA:1590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001629	ORPHA:99094	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001659	ORPHA:99094	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0025578	ORPHA:99094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0031567	ORPHA:99094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001635	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001962	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0002875	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0006704	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0011645	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0011681	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0012378	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0012663	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0031668	ORPHA:99094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001712	ORPHA:99094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0004970	ORPHA:99094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0011682	ORPHA:99094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0100749	ORPHA:99094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001643	ORPHA:99094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001647	ORPHA:99094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001655	ORPHA:99094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0001705	ORPHA:99094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99094	Laubry-Pezzi syndrome		HP:0004890	ORPHA:99094	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001629	ORPHA:99095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0012382	ORPHA:99095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001635	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001667	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001708	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001785	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001945	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001962	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0002094	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0005168	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0006689	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0011682	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0012378	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0012398	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0030718	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0030830	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0031443	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0031664	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0031667	ORPHA:99095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001324	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0001642	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0002092	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0002563	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0002617	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0005180	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0010741	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0030848	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99095	Congenital Gerbode defect		HP:0100749	ORPHA:99095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000322	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000411	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000668	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000750	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0001156	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0001249	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0001263	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0004322	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0009738	ORPHA:1598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000175	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000248	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000252	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000286	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000347	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000400	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000431	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000465	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000470	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000508	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000670	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000692	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000767	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000822	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0001252	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0002162	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0002714	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0002751	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0006610	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0100625	ORPHA:1598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000568	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000708	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0000821	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0001004	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0001360	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0001596	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0002960	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0007325	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1598	Monosomy 18p syndrome		HP:0030680	ORPHA:1598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000160	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000252	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000288	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000316	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000358	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000582	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000648	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0000995	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0001172	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0001622	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0001626	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0001643	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0001671	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0002093	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0002240	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0002983	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0003272	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0003312	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0004097	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0004322	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0005487	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0005916	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0007477	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0007598	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0008551	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0009601	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0010293	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0010306	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0100555	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0100560	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1597	Distal deletion 17q syndrome		HP:0200055	ORPHA:1597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001511	ORPHA:1596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001518	ORPHA:1596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000028	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000047	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000054	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000164	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000175	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000219	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000252	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000280	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000316	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000322	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000325	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000347	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000365	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000369	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000455	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000486	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000581	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000582	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000729	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000750	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000776	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001250	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001263	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001508	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001510	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001647	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001680	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001718	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001762	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001792	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0002089	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0002761	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0002827	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0002857	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0004322	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001671	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0005469	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0005709	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0007018	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0008897	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0009381	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0009882	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0010297	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0012303	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0030353	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0030918	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0040019	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0200055	ORPHA:1596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000003	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000476	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0000954	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001195	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0001643	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0004383	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0004471	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0011560	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0011651	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1596	Distal deletion 15q syndrome		HP:0100542	ORPHA:1596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0200063	ORPHA:160148	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0002019	ORPHA:160148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0002027	ORPHA:160148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0002573	ORPHA:160148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0002582	ORPHA:160148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0001824	ORPHA:160148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0002014	ORPHA:160148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160148	Cap polyposis		HP:0003270	ORPHA:160148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79492	Pili gemini		HP:0003329	ORPHA:79492	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79492	Pili gemini		HP:0003328	ORPHA:79492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0031024	ORPHA:79493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0000271	ORPHA:79493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0000464	ORPHA:79493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0001965	ORPHA:79493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0012842	ORPHA:79493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0025367	ORPHA:79493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0200036	ORPHA:79493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0001892	ORPHA:79493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0002671	ORPHA:79493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0007606	ORPHA:79493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0010732	ORPHA:79493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0025512	ORPHA:79493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0200042	ORPHA:79493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0000365	ORPHA:79493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0000372	ORPHA:79493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0000505	ORPHA:79493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0010287	ORPHA:79493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0010288	ORPHA:79493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0010628	ORPHA:79493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79493	Brooke-Spiegler syndrome		HP:0100684	ORPHA:79493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002172	ORPHA:37612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002311	ORPHA:37612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002411	ORPHA:37612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0000622	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0000651	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0000975	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0001260	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002018	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002312	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002315	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002321	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0003394	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0003552	ORPHA:37612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0000750	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0001188	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0001266	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0001270	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0001272	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0001276	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0001328	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002098	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002486	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002650	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0002751	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0005461	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0008981	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37612	Episodic ataxia type 1		HP:0030051	ORPHA:37612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34587	Danon disease		HP:0001249	ORPHA:34587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34587	Danon disease		HP:0001288	ORPHA:34587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34587	Danon disease		HP:0001639	ORPHA:34587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34587	Danon disease		HP:0001644	ORPHA:34587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34587	Danon disease		HP:0006543	ORPHA:34587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34587	Danon disease		HP:0010547	ORPHA:34587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001817	ORPHA:79499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0008625	ORPHA:79499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0000164	ORPHA:79499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0000677	ORPHA:79499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001199	ORPHA:79499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001802	ORPHA:79499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0008386	ORPHA:79499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0000268	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0000348	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001057	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001249	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001250	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001763	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001800	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0001999	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0002465	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0009778	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0012554	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0200104	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79499	Autosomal dominant deafness-onychodystrophy syndrome		HP:0200141	ORPHA:79499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000028	ORPHA:1580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000431	ORPHA:1580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000444	ORPHA:1580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0001249	ORPHA:1580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0011344	ORPHA:1580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000252	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000316	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000347	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000364	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000365	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000358	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000400	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000470	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000486	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000494	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0001511	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0001800	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0004209	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0004322	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0007598	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0030680	ORPHA:1580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000147	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000175	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0000465	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0001231	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0001387	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0002023	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0004397	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0008736	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0009811	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1580	Distal deletion 10p syndrome		HP:0100335	ORPHA:1580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000750	ORPHA:544254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001249	ORPHA:544254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001263	ORPHA:544254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0002197	ORPHA:544254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0010832	ORPHA:544254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000708	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000729	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001251	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001252	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001288	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001999	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0002342	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0002360	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0002311	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0002376	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0002465	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0010864	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0020208	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0100738	ORPHA:544254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000047	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000154	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000160	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000218	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000233	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000252	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000276	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000325	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000400	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000490	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0012760	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0000992	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001337	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0001344	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0008770	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0008872	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0011150	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0012703	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0030810	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0040080	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0100023	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544254	SYNGAP1-related developmental and epileptic encephalopathy		HP:0100259	ORPHA:544254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000252	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000316	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000391	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000426	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000431	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0001249	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0001511	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0004322	ORPHA:1587	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000243	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000286	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000347	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000369	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000411	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000470	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000508	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000518	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000568	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000612	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0001156	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0001252	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0004209	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0006101	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0007477	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0009919	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0030680	ORPHA:1587	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0000465	ORPHA:1587	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0001360	ORPHA:1587	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0002079	ORPHA:1587	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0009601	ORPHA:1587	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1587	Monosomy 13q14 syndrome		HP:0011024	ORPHA:1587	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0002960	ORPHA:79480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0011355	ORPHA:79480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0025300	ORPHA:79480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0025474	ORPHA:79480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0100792	ORPHA:79480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0003493	ORPHA:79480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0008066	ORPHA:79480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0031540	ORPHA:79480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0000155	ORPHA:79480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0001053	ORPHA:79480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0002725	ORPHA:79480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0007510	ORPHA:79480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0030208	ORPHA:79480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79480	Pemphigus erythematosus		HP:0200041	ORPHA:79480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0002960	ORPHA:79481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0100792	ORPHA:79481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0000989	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0001965	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0007473	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0008066	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0010783	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0025474	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0040189	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0200041	ORPHA:79481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0000155	ORPHA:79481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0001019	ORPHA:79481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0011830	ORPHA:79481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0200037	ORPHA:79481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0003765	ORPHA:79481	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0004377	ORPHA:79481	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0008069	ORPHA:79481	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0025527	ORPHA:79481	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0025528	ORPHA:79481	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79481	Pemphigus foliaceus		HP:0200039	ORPHA:79481	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0000286	ORPHA:1581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0000431	ORPHA:1581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0000486	ORPHA:1581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0000508	ORPHA:1581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0000582	ORPHA:1581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0000664	ORPHA:1581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0001156	ORPHA:1581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0001251	ORPHA:1581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0001252	ORPHA:1581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0001288	ORPHA:1581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0004209	ORPHA:1581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0004422	ORPHA:1581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0007598	ORPHA:1581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0010557	ORPHA:1581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1581	Non-distal deletion 10q syndrome		HP:0100543	ORPHA:1581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0000572	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0000613	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0006758	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0007663	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0007830	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0007984	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0007987	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0030057	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0030357	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0030786	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0033020	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0100013	ORPHA:71505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0000543	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0000603	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0001105	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0001133	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0004377	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0007641	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0007722	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0007793	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0010784	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0010788	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0012189	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0030528	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0030627	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0100275	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0100522	ORPHA:71505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0000648	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0002367	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0002894	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0003003	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0006725	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0011531	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0012056	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71505	Cancer-associated retinopathy		HP:0012125	ORPHA:71505	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000028	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000033	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000037	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000127	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000144	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000151	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000771	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000823	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000848	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000939	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0001197	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0001274	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0001508	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0001941	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0001944	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0001998	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0002013	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0002153	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0002615	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0002750	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0002902	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0003107	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0003154	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0004319	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0004349	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0007440	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0007574	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008073	ORPHA:289548	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008163	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008187	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008207	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008730	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008734	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0010789	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0011106	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0011749	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0011968	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0012244	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0012245	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0012598	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0012605	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0030349	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0030369	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0100779	ORPHA:289548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000835	ORPHA:289548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0001622	ORPHA:289548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008232	ORPHA:289548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0011969	ORPHA:289548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0000142	ORPHA:289548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0008665	ORPHA:289548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0010512	ORPHA:289548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289548	Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency		HP:0012854	ORPHA:289548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0000639	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0001256	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0001258	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0002061	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0002064	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0002166	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0001288	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0002509	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401800	Autosomal recessive spastic paraplegia type 60		HP:0007002	ORPHA:401800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0002061	ORPHA:488594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0002395	ORPHA:488594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0003487	ORPHA:488594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0001251	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0001260	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0001761	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0002066	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0003202	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0007340	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0007350	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0009830	ORPHA:488594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0000009	ORPHA:488594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0000496	ORPHA:488594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0002070	ORPHA:488594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0002650	ORPHA:488594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0008081	ORPHA:488594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488594	Autosomal recessive spastic paraplegia type 76		HP:0011448	ORPHA:488594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0001257	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0001276	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0001347	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0002194	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0003202	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0004322	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0004325	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0012407	ORPHA:401805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401805	Autosomal recessive spastic paraplegia type 63		HP:0002518	ORPHA:401805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0000338	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0000473	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0001260	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0001270	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0001300	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002015	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002066	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002067	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002172	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002300	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002307	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002451	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0012179	ORPHA:71517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0000712	ORPHA:71517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0000716	ORPHA:71517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0000739	ORPHA:71517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0001250	ORPHA:71517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0001272	ORPHA:71517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0002322	ORPHA:71517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71517	Rapid-onset dystonia-parkinsonism		HP:0001290	ORPHA:71517	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0000473	ORPHA:71518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0002457	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0000737	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0000741	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0000980	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0001251	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0002013	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0002076	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0002321	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71518	Benign paroxysmal torticollis of infancy		HP:0002329	ORPHA:71518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71519	Psychogenic movement disorders		HP:0001288	ORPHA:71519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71519	Psychogenic movement disorders		HP:0002167	ORPHA:71519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71519	Psychogenic movement disorders		HP:0100022	ORPHA:71519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1574	Retinal degeneration-nanophthalmos-glaucoma syndrome		HP:0000505	ORPHA:1574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1574	Retinal degeneration-nanophthalmos-glaucoma syndrome		HP:0000512	ORPHA:1574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1574	Retinal degeneration-nanophthalmos-glaucoma syndrome		HP:0000545	ORPHA:1574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1574	Retinal degeneration-nanophthalmos-glaucoma syndrome		HP:0000568	ORPHA:1574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1574	Retinal degeneration-nanophthalmos-glaucoma syndrome		HP:0000639	ORPHA:1574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1574	Retinal degeneration-nanophthalmos-glaucoma syndrome		HP:0000648	ORPHA:1574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1574	Retinal degeneration-nanophthalmos-glaucoma syndrome		HP:0007703	ORPHA:1574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0000608	ORPHA:1573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0000618	ORPHA:1573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0000639	ORPHA:1573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0000962	ORPHA:1573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0000995	ORPHA:1573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0001480	ORPHA:1573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0002209	ORPHA:1573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0002213	ORPHA:1573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0002299	ORPHA:1573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0002652	ORPHA:1573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0002813	ORPHA:1573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0003777	ORPHA:1573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0004322	ORPHA:1573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0008002	ORPHA:1573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1573	Hypotrichosis with juvenile macular degeneration		HP:0100326	ORPHA:1573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000541	ORPHA:1571	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000545	ORPHA:1571	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000608	ORPHA:1571	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0001362	ORPHA:1571	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0002085	ORPHA:1571	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000238	ORPHA:1571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000529	ORPHA:1571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000572	ORPHA:1571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000639	ORPHA:1571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0004327	ORPHA:1571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0007773	ORPHA:1571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000076	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000286	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000486	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0000518	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0001083	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0001250	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0001595	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0001643	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0001651	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0002021	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0005280	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0001382	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0011800	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0030037	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1571	Knobloch syndrome		HP:0100764	ORPHA:1571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0009800	ORPHA:1570	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0100745	ORPHA:1570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0002650	ORPHA:1570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0031095	ORPHA:1570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0003422	ORPHA:1570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0006501	ORPHA:1570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0009601	ORPHA:1570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1570	Symbrachydactyly of hands and feet		HP:0040071	ORPHA:1570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0000590	ORPHA:276238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0001332	ORPHA:276238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002071	ORPHA:276238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002073	ORPHA:276238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002493	ORPHA:276238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0007256	ORPHA:276238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0009830	ORPHA:276238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0000520	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0000623	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0000640	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0000651	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0000750	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0001257	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0001260	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0001272	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0001347	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002198	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002312	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002503	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0003202	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0003487	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0007089	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0007240	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0011960	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0040140	ORPHA:276238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0000011	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0001605	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0001751	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002015	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002354	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0002360	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0003394	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0004370	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276238	Machado-Joseph disease type 1		HP:0008944	ORPHA:276238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0005353	ORPHA:33276	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001034	ORPHA:33276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0002814	ORPHA:33276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0008069	ORPHA:33276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0012733	ORPHA:33276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0000479	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001028	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001298	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001743	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0002721	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0005523	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0008940	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0011024	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0200034	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0200036	ORPHA:33276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0000988	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001004	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001392	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001824	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0001945	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0002014	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0002088	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0005293	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0011793	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0012378	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33276	Kaposi sarcoma		HP:0200035	ORPHA:33276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002027	ORPHA:79473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0010472	ORPHA:79473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0010473	ORPHA:79473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0012217	ORPHA:79473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0012379	ORPHA:79473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000707	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000708	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000739	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000992	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001324	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002019	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002273	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0003163	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0003418	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0007178	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0008066	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0008997	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0100749	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0200037	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0200041	ORPHA:79473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000011	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000822	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000953	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000998	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001010	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001056	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001072	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001250	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001265	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001347	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001649	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002018	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002203	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002595	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002902	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0002910	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0003474	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0011355	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0012332	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0031218	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0100699	ORPHA:79473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0000738	ORPHA:79473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001259	ORPHA:79473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001392	ORPHA:79473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001402	ORPHA:79473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0001903	ORPHA:79473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0011999	ORPHA:79473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79473	Variegate porphyria		HP:0012622	ORPHA:79473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000035	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000135	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000144	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000233	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000275	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000347	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000444	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000519	ORPHA:79474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000546	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000765	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000819	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000822	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000823	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000831	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000905	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000842	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000869	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000934	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000939	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000962	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0000963	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001015	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0009771	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001376	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001385	ORPHA:79474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001397	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001508	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004322	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001595	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001596	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001601	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001608	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001634	ORPHA:79474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001635	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001650	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001677	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001763	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001808	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0001838	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0002155	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0002211	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0002216	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0002231	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0002669	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0002858	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0003074	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0003076	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0003202	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0008981	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0003738	ORPHA:79474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0003777	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004054	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004279	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004325	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004349	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004361	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004380	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004414	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0004950	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0005109	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0005177	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0005328	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0005978	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0007509	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0007495	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0007618	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0007703	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0008065	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0008069	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0008209	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0008283	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0008419	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0009064	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0009726	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0010721	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0011001	ORPHA:79474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0011362	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0040019	ORPHA:79474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100013	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100031	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100526	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100578	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100585	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100615	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100649	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100659	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100679	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100833	ORPHA:79474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0100840	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79474	Atypical Werner syndrome		HP:0200042	ORPHA:79474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0000488	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0000639	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0000651	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0001249	ORPHA:79476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0001250	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0001251	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0001263	ORPHA:79476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0001276	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0001290	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0002216	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0002514	ORPHA:79476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0003077	ORPHA:79476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0007443	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0007730	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0011364	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79476	Griscelli syndrome type 1		HP:0100022	ORPHA:79476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0000952	ORPHA:79477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0000967	ORPHA:79477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0001250	ORPHA:79477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0001276	ORPHA:79477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0001744	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0001875	ORPHA:79477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0001876	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0001945	ORPHA:79477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0002017	ORPHA:79477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0002113	ORPHA:79477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0002216	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0002240	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0002716	ORPHA:79477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0002721	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0003077	ORPHA:79477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0005599	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0007443	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0007730	ORPHA:79477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79477	Griscelli syndrome type 2		HP:0012156	ORPHA:79477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79478	Griscelli syndrome type 3		HP:0005599	ORPHA:79478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79478	Griscelli syndrome type 3		HP:0007443	ORPHA:79478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79478	Griscelli syndrome type 3		HP:0007730	ORPHA:79478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0004923	ORPHA:1578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0040210	ORPHA:1578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0010553	ORPHA:1578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0040206	ORPHA:1578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0000737	ORPHA:1578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0001276	ORPHA:1578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0001337	ORPHA:1578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0002917	ORPHA:1578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0008936	ORPHA:1578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0012758	ORPHA:1578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0001300	ORPHA:1578	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0004904	ORPHA:1578	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1578	Pterin-4 alpha-carbinolamine dehydratase deficiency		HP:0100021	ORPHA:1578	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0002166	ORPHA:209004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0007133	ORPHA:209004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0011402	ORPHA:209004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0002936	ORPHA:209004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0003693	ORPHA:209004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0005508	ORPHA:209004	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0007002	ORPHA:209004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0007220	ORPHA:209004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0007267	ORPHA:209004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0007340	ORPHA:209004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0100287	ORPHA:209004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0003390	ORPHA:209004	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0007240	ORPHA:209004	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0012514	ORPHA:209004	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0031006	ORPHA:209004	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0002665	ORPHA:209004	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0006775	ORPHA:209004	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0025346	ORPHA:209004	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:209004	Polyneuropathy associated with IgM monoclonal gammopathy		HP:0100778	ORPHA:209004	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0000252	ORPHA:401810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0000718	ORPHA:401810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0000823	ORPHA:401810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0001257	ORPHA:401810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0001260	ORPHA:401810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0001288	ORPHA:401810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0006889	ORPHA:401810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0001284	ORPHA:401810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401810	Autosomal recessive spastic paraplegia type 64		HP:0002500	ORPHA:401810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0001249	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0001284	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0001301	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0001321	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0001762	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0002061	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0002064	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0002079	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0002166	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0001288	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0002509	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0007020	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0007210	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401815	Autosomal recessive spastic paraplegia type 66		HP:0030048	ORPHA:401815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000625	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000653	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0001156	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0001274	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0002006	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0005258	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0005466	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0009119	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0011803	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0040019	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0045075	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0100490	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0001249	ORPHA:306542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0001636	ORPHA:306542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0004423	ORPHA:306542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0006931	ORPHA:306542	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000175	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000286	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000316	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000327	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000349	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000358	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000384	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000405	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000430	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000431	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000508	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000518	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306542	Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		HP:0000568	ORPHA:306542	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000526	ORPHA:250923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000572	ORPHA:250923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000639	ORPHA:250923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0007663	ORPHA:250923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0007676	ORPHA:250923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0007750	ORPHA:250923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0008059	ORPHA:250923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000486	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000501	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000518	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000642	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000659	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0001083	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0001097	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0007894	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0007957	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0011496	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0030466	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0030468	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0030622	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0032107	ORPHA:250923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000508	ORPHA:250923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000568	ORPHA:250923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000609	ORPHA:250923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0000613	ORPHA:250923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0030961	ORPHA:250923	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:250923	Isolated aniridia		HP:0100719	ORPHA:250923	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1566	Dandy-Walker malformation-postaxial polydactyly syndrome		HP:0001162	ORPHA:1566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1566	Dandy-Walker malformation-postaxial polydactyly syndrome		HP:0001305	ORPHA:1566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0001257	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0001258	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0001288	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0001347	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0012332	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0003409	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0007328	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0009830	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0200042	ORPHA:139578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0002143	ORPHA:139578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0002169	ORPHA:139578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0003390	ORPHA:139578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0003431	ORPHA:139578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0003487	ORPHA:139578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0003693	ORPHA:139578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0007020	ORPHA:139578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0001886	ORPHA:139578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139578	Mutilating hereditary sensory neuropathy with spastic paraplegia		HP:0006121	ORPHA:139578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0000248	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0000252	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0000280	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0000750	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0001357	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0001558	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0001662	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0002342	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0002506	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0005469	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0007000	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0007281	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0010864	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2898	X-linked intellectual disability-plagiocephaly syndrome		HP:0011220	ORPHA:2898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000083	ORPHA:1563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000112	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000431	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000506	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000518	ORPHA:1563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000821	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000829	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0000966	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0001004	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0001072	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0001156	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0001634	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0001798	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0002230	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0002901	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0004322	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1563	Dahlberg-Borer-Newcomer syndrome		HP:0009882	ORPHA:1563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000707	ORPHA:1560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001250	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002514	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002922	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0003474	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0004302	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0010576	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0010651	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0010702	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0011805	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0012443	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0012703	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0100702	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0200149	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0410234	ORPHA:1560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000651	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000708	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000712	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000738	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000925	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000929	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000933	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001637	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002133	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002197	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002354	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002493	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002516	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0006824	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0007359	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0009745	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0012372	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0025258	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0100249	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0100561	ORPHA:1560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000541	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000726	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0000741	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001094	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001251	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001260	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001268	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001289	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0001297	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0002383	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0004420	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0007185	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0012424	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1560	Cysticercosis		HP:0025163	ORPHA:1560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0000968	ORPHA:2890	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0000175	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0000377	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0000561	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0000958	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0000964	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0000982	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0001596	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0002223	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0002289	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0002299	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0002552	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0007439	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0008394	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0008404	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0010562	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0012725	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0030953	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0410030	ORPHA:2890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2890	Pili torti-onychodysplasia syndrome		HP:0002231	ORPHA:2890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0001251	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0001252	ORPHA:2891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0001263	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0001288	ORPHA:2891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0001510	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0003777	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0001382	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0010719	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0100840	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2891	Pili torti-developmental delay-neurological abnormalities syndrome		HP:0200102	ORPHA:2891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0003487	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0007089	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0007240	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0007256	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0011960	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0040140	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0000011	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0001605	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0001751	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002015	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002354	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002360	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0003394	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0003477	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0004370	ORPHA:276244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0000590	ORPHA:276244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002071	ORPHA:276244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002073	ORPHA:276244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0008944	ORPHA:276244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0000520	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0000623	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0000640	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0000651	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0000750	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0001257	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0001260	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0001272	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0001332	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0001347	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002198	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002312	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002366	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002398	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002460	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002493	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0002503	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0003202	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276244	Machado-Joseph disease type 3		HP:0003457	ORPHA:276244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1568	X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome		HP:0000023	ORPHA:1568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1568	X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome		HP:0000028	ORPHA:1568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1568	X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome		HP:0000256	ORPHA:1568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1568	X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome		HP:0000486	ORPHA:1568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1568	X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome		HP:0002119	ORPHA:1568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1568	X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome		HP:0002120	ORPHA:1568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1568	X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome		HP:0007360	ORPHA:1568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000154	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000174	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000252	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000280	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000293	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000322	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000341	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000391	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000426	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000463	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000470	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000483	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000490	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000545	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000582	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000692	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000954	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001182	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001249	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001251	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001252	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001263	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001328	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001508	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001510	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001763	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002019	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002020	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002036	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002300	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002342	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002360	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002381	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0006352	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0008081	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0010529	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0010743	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0011039	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0011300	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0011833	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0011968	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0012471	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0040019	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0100633	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0200055	ORPHA:2896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000451	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000486	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001063	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001250	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001344	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001786	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002066	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002472	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002793	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002883	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0007370	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0010535	ORPHA:2896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000028	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000054	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000718	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0000729	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0001053	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002558	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002650	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0008897	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0040082	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0100716	ORPHA:2896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0002251	ORPHA:2896	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2896	Pitt-Hopkins syndrome		HP:0012189	ORPHA:2896	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0000163	ORPHA:2897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0000964	ORPHA:2897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0000982	ORPHA:2897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0000989	ORPHA:2897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0001019	ORPHA:2897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0001072	ORPHA:2897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0001597	ORPHA:2897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0002664	ORPHA:2897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0007400	ORPHA:2897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0008064	ORPHA:2897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0008392	ORPHA:2897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0100725	ORPHA:2897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0200034	ORPHA:2897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2897	Pityriasis rubra pilaris		HP:0200039	ORPHA:2897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0000590	ORPHA:276241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002071	ORPHA:276241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002073	ORPHA:276241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0000520	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0000623	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0000640	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0000651	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0000750	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0001257	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0001260	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0001272	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0001332	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0001347	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002198	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002312	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002493	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002503	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0003202	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0003487	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0007089	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0007240	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0007256	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0009830	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0011960	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0040140	ORPHA:276241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0000011	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0001605	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0001751	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002015	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002354	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0002360	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0003394	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0004370	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276241	Machado-Joseph disease type 2		HP:0008944	ORPHA:276241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0001256	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0001263	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0001274	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0001347	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0002061	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0002064	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0002120	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0001288	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0003487	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0003700	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0006817	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0007020	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0012447	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0100022	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401820	Autosomal recessive spastic paraplegia type 67		HP:0200085	ORPHA:401820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000414	ORPHA:363965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000447	ORPHA:363965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000750	ORPHA:363965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001252	ORPHA:363965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001263	ORPHA:363965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001999	ORPHA:363965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0100025	ORPHA:363965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000028	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000047	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000119	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000232	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000276	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000286	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000365	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000400	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000411	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000486	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000505	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000508	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000540	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000582	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000708	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000968	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001250	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001256	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001319	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001373	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001382	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001382	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001518	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001627	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001761	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001763	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001848	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002011	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002119	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002342	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002353	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0005656	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0007359	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0008897	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0011182	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0011185	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0011968	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0012433	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0012443	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0012745	ORPHA:363965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000010	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000075	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000076	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000126	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000194	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000238	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000256	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000403	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000426	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000430	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000431	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000519	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000581	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000648	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000729	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000739	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000748	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000767	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000768	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000826	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000957	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000960	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000962	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000964	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001010	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001045	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001054	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001166	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001212	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001274	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001363	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001533	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001596	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001601	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001629	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001631	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001638	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001642	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001647	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002079	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002197	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002205	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002286	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002414	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002650	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002652	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002779	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002808	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0003302	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0003307	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0004942	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0005216	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0006482	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0006813	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0007018	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0007099	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0008064	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0008207	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0008445	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0009130	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0009928	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0010864	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0010945	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0011098	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0011470	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0011822	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0012683	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0012699	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0025268	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0030746	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0100775	ORPHA:363965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000252	ORPHA:363965	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000821	ORPHA:363965	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0000824	ORPHA:363965	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0001028	ORPHA:363965	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0002861	ORPHA:363965	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363965	Koolen-De Vries syndrome due to a point mutation		HP:0010788	ORPHA:363965	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001249	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002013	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002020	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002360	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002487	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0008762	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0025152	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000219	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000244	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000286	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000319	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000349	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000540	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000713	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000729	ORPHA:522077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001270	ORPHA:522077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001344	ORPHA:522077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002353	ORPHA:522077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0008947	ORPHA:522077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0011344	ORPHA:522077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000486	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000565	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000639	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000733	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000817	ORPHA:522077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000739	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0000742	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001251	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001266	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001332	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001382	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001601	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001631	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0001776	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002072	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002465	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002650	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002871	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002883	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0002938	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0003196	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0004691	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0004879	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0005274	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0005876	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0007874	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0008081	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0008138	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0010535	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0010850	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0011194	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0011196	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0011228	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0011445	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0011968	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0012169	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0012448	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0025247	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0040296	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:522077	Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome		HP:0100248	ORPHA:522077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002027	ORPHA:583861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0030248	ORPHA:583861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0001974	ORPHA:583861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002013	ORPHA:583861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002014	ORPHA:583861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002018	ORPHA:583861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002039	ORPHA:583861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0001081	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0001541	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0001945	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002151	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002239	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0002615	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0003270	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0030151	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0031273	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0100806	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:0410282	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583861	Isolated mesenteric vein thrombosis		HP:6000377	ORPHA:583861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000028	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000048	ORPHA:1555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000160	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000175	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000189	ORPHA:1555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000238	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000262	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000268	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000271	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000272	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000316	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000364	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000391	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000400	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000453	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000463	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000478	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000494	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000504	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000508	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000520	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000648	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000822	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000929	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000956	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000982	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0000995	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0001363	ORPHA:1555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0001482	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0001537	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0001545	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0001597	ORPHA:1555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0001732	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0002098	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0002676	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0003246	ORPHA:1555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0004450	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0005280	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0007469	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0009804	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0009906	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0010669	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0011800	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1555	Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome		HP:0100761	ORPHA:1555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0000316	ORPHA:1553	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0000324	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0000568	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0000588	ORPHA:1553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0000612	ORPHA:1553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0001053	ORPHA:1553	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0001177	ORPHA:1553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0001249	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0001274	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0001363	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0001770	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0001829	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0002119	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0002230	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0002566	ORPHA:1553	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0006101	ORPHA:1553	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0008065	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0009602	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1553	Curry-Jones syndrome		HP:0011304	ORPHA:1553	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0000164	ORPHA:2889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0000365	ORPHA:2889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0000534	ORPHA:2889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0000682	ORPHA:2889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0001596	ORPHA:2889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0001597	ORPHA:2889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0002299	ORPHA:2889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0003777	ORPHA:2889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2889	Pili torti		HP:0010719	ORPHA:2889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0000708	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0001257	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0001260	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0001268	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0001324	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002063	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002172	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002378	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0003487	ORPHA:289560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0000020	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0000648	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0001288	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0001300	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0001332	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002015	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002067	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002313	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002359	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002453	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002607	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0006801	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0007002	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0045007	ORPHA:289560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0000570	ORPHA:289560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002362	ORPHA:289560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289560	Mitochondrial membrane protein-associated neurodegeneration		HP:0002093	ORPHA:289560	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0001873	ORPHA:244242	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0002910	ORPHA:244242	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0001878	ORPHA:244242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0000093	ORPHA:244242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0002315	ORPHA:244242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0004324	ORPHA:244242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0007430	ORPHA:244242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0008071	ORPHA:244242	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0008151	ORPHA:244242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0011900	ORPHA:244242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0012378	ORPHA:244242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0100602	ORPHA:244242	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0001058	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0001937	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0002013	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0002018	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0002027	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0002202	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0002615	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0003418	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0003641	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0005521	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0011419	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0025435	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0025547	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0030834	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0100598	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0100601	ORPHA:244242	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0410019	ORPHA:244242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0001342	ORPHA:244242	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0001919	ORPHA:244242	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:244242	HELLP syndrome		HP:0011029	ORPHA:244242	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0008517	ORPHA:1552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0030736	ORPHA:1552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0002023	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0002025	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0003270	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0003419	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0007293	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0009790	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0012450	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0032155	ORPHA:1552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0000011	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0000076	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0000085	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0000125	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0000238	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0000813	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0001153	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0002144	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0002242	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0009793	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0010447	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0012033	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0025247	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0030451	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0034231	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0200040	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:6000336	ORPHA:1552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0000010	ORPHA:1552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0001287	ORPHA:1552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1552	Currarino syndrome		HP:0100559	ORPHA:1552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0000431	ORPHA:1551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0001061	ORPHA:1551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0001250	ORPHA:1551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0001252	ORPHA:1551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0001903	ORPHA:1551	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0002002	ORPHA:1551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0002234	ORPHA:1551	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0004322	ORPHA:1551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0005019	ORPHA:1551	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0008060	ORPHA:1551	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0010978	ORPHA:1551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1551	Familial benign copper deficiency		HP:0011967	ORPHA:1551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000238	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000252	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000365	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000488	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000639	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000648	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000958	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000988	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000992	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001025	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001029	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001249	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001251	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001257	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0002634	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0004322	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0004326	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0004334	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0004337	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0007495	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0007587	ORPHA:220295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0000651	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001260	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001263	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0001289	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0002671	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0002861	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0006739	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:220295	Xeroderma pigmentosum-Cockayne syndrome complex		HP:0007108	ORPHA:220295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0012758	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0000252	ORPHA:2880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001987	ORPHA:2880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001988	ORPHA:2880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0002151	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0002173	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0003128	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0003217	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0003648	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0012402	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0031956	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0031964	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0034648	ORPHA:2880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001252	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001254	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001325	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001397	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001410	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0001998	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0002013	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0002329	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2880	Phosphoenolpyruvate carboxykinase deficiency		HP:0006846	ORPHA:2880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0000991	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0001744	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0001878	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0001902	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0002829	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0002910	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0003124	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0004446	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0005181	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0033341	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0040185	ORPHA:2882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0001650	ORPHA:2882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2882	Sitosterolemia		HP:0005059	ORPHA:2882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0002211	ORPHA:2884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0005599	ORPHA:2884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0007544	ORPHA:2884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0001053	ORPHA:2884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0002226	ORPHA:2884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0002227	ORPHA:2884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0012733	ORPHA:2884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0000252	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0000343	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0000365	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0000431	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0000664	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0001100	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0001249	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0001251	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0001252	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0002251	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0002683	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2884	Piebaldism		HP:0008069	ORPHA:2884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0000407	ORPHA:2885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0000499	ORPHA:2885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0000534	ORPHA:2885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0000992	ORPHA:2885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0001029	ORPHA:2885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0001053	ORPHA:2885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0001100	ORPHA:2885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0001249	ORPHA:2885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0001251	ORPHA:2885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0002251	ORPHA:2885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0005599	ORPHA:2885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0007400	ORPHA:2885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0008069	ORPHA:2885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2885	Piebald trait-neurologic defects syndrome		HP:0012733	ORPHA:2885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000003	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000202	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000347	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000541	ORPHA:1556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000555	ORPHA:1556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000821	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000951	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000965	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0000979	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0001250	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0001511	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0001541	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0001643	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0001770	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0001933	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0002650	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0002814	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0002817	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0004349	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0005306	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0006101	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0006385	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0007565	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0008065	ORPHA:1556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0100026	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0100543	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0100545	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0100555	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0100585	ORPHA:1556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0100627	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0100814	ORPHA:1556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1556	Cutis marmorata telangiectatica congenita		HP:0200041	ORPHA:1556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000201	ORPHA:2886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001631	ORPHA:2886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001762	ORPHA:2886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0005301	ORPHA:2886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000162	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000175	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000316	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000340	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000347	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000431	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000961	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001249	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001263	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001290	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001508	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001511	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001838	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0009891	ORPHA:2886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000028	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000085	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000126	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000239	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000365	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000358	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000385	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000395	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000463	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000545	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000574	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000954	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001161	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001250	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001273	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001321	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001978	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0002104	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0002136	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0002650	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0004492	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0006101	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0006434	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0009738	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0012745	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0030084	ORPHA:2886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000199	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000648	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000767	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0000879	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0001636	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0002089	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0002246	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0009085	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0010720	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0011445	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2886	TARP syndrome		HP:0100259	ORPHA:2886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0000365	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0000518	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0001256	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0001263	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0001274	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0002061	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0002120	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0002378	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0002464	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0006817	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0007020	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0012447	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401830	Autosomal recessive spastic paraplegia type 69		HP:0100022	ORPHA:401830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0001256	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0001263	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0002061	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0002378	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0006530	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0007020	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0009830	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0012447	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0100022	ORPHA:401835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401835	Autosomal recessive spastic paraplegia type 70		HP:0000100	ORPHA:401835	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0000358	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0000369	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0000772	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0001059	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0001511	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0003312	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0003316	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0009465	ORPHA:2876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0000286	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0000396	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0000405	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0000494	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0001199	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0001387	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0001629	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0001680	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0002475	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0002974	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0004935	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0005280	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0009778	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0009906	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0010059	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0011304	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0012304	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2876	PHAVER syndrome		HP:0100490	ORPHA:2876	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0000028	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0000151	ORPHA:2879	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0000175	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0000347	ORPHA:2879	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0000411	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0000470	ORPHA:2879	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0009380	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0001362	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0001511	ORPHA:2879	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0001789	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0001849	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0001883	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002023	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002164	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002435	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002575	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002705	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002983	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002984	ORPHA:2879	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002986	ORPHA:2879	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002990	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0002992	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0003041	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0003196	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0003498	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0003982	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0006487	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0008517	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0008736	ORPHA:2879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0009103	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2879	Phocomelia, Schinzel type		HP:0100257	ORPHA:2879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000174	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000262	ORPHA:1540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000303	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000316	ORPHA:1540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000327	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000444	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000486	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000508	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0000520	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0001770	ORPHA:1540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0001783	ORPHA:1540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0001839	ORPHA:1540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0001841	ORPHA:1540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0002007	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0002991	ORPHA:1540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0004691	ORPHA:1540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0009773	ORPHA:1540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0009891	ORPHA:1540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0010059	ORPHA:1540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0010743	ORPHA:1540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1540	Jackson-Weiss syndrome		HP:0011800	ORPHA:1540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0000286	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0000377	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0000581	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0001249	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0001387	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0001620	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0004322	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome		HP:0006297	ORPHA:2871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2871	Pfeiffer-Palm-Teller syndrome	NOT	HP:0001650	ORPHA:2871	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0000035	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0000047	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0000164	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0000268	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0000486	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0000768	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0001166	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0001249	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0001252	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0001387	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0001608	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0002205	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0002650	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0002750	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0002808	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0006703	ORPHA:1548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1548	Cryptorchidism-arachnodactyly-intellectual disability syndrome		HP:0007598	ORPHA:1548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000863	ORPHA:95513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000871	ORPHA:95513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0011751	ORPHA:95513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000141	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000622	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000802	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000870	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000980	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0001278	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0001895	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0001959	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0002018	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0002315	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0003158	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0007987	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0008163	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0008213	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0008214	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0008240	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0008245	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0011735	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0011748	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0012504	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0012696	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0030018	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0040171	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0040306	ORPHA:95513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000407	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000651	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0000872	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0002902	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0003493	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0004396	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0007041	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95513	Panhypophysitis		HP:0008202	ORPHA:95513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000358	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000431	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000473	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000494	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0001238	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0001249	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0001537	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000347	ORPHA:2872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000369	ORPHA:2872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0001263	ORPHA:2872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0001510	ORPHA:2872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0001511	ORPHA:2872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0004442	ORPHA:2872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0012478	ORPHA:2872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000028	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000047	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000054	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000193	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000268	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000289	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0000316	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0001627	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0002705	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0002778	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0002876	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0004322	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0006191	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0008070	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0008112	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0009540	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0010487	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0010621	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0010721	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2872	Cardiocranial syndrome, Pfeiffer type		HP:0011220	ORPHA:2872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1547	Cryptomicrotia-brachydactyly-excess fingertip arch syndrome		HP:0000048	ORPHA:1547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1547	Cryptomicrotia-brachydactyly-excess fingertip arch syndrome		HP:0000506	ORPHA:1547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1547	Cryptomicrotia-brachydactyly-excess fingertip arch syndrome		HP:0001480	ORPHA:1547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1547	Cryptomicrotia-brachydactyly-excess fingertip arch syndrome		HP:0001800	ORPHA:1547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1547	Cryptomicrotia-brachydactyly-excess fingertip arch syndrome		HP:0005872	ORPHA:1547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1547	Cryptomicrotia-brachydactyly-excess fingertip arch syndrome		HP:0007477	ORPHA:1547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1547	Cryptomicrotia-brachydactyly-excess fingertip arch syndrome		HP:0009882	ORPHA:1547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0001945	ORPHA:1546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002721	ORPHA:1546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0012735	ORPHA:1546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0025392	ORPHA:1546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000238	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000478	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000504	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000708	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0001268	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0001287	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0001394	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002013	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002090	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002094	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002098	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002120	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002202	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002315	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002516	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002664	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002725	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002960	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0003690	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0031179	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0100721	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0100749	ORPHA:1546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000024	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000356	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000479	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000587	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000602	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0000618	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0001250	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0001291	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002181	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002354	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002586	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002754	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0002797	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0005526	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0011531	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1546	Cryptococcosis		HP:0100806	ORPHA:1546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0010817	ORPHA:2874	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0025510	ORPHA:2874	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0002650	ORPHA:2874	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0000995	ORPHA:2874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0002671	ORPHA:2874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0002859	ORPHA:2874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0004912	ORPHA:2874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0012758	ORPHA:2874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0100556	ORPHA:2874	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0000028	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0000501	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0000589	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0000826	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0000975	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0001004	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0001028	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0001250	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0001269	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0001347	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0001528	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0002232	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0002414	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0002666	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0002667	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0011675	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0012056	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0012583	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0030409	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0030880	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0100702	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0100814	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2874	Phakomatosis pigmentokeratotica		HP:0100963	ORPHA:2874	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000160	ORPHA:1545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000218	ORPHA:1545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000293	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000343	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000347	ORPHA:1545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000445	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000463	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000966	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0000975	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0001250	ORPHA:1545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0001276	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0001371	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0001376	ORPHA:1545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0001522	ORPHA:1545	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0001645	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0002047	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0002093	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0002650	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0002808	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0011968	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0100490	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0100543	ORPHA:1545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1545	Crisponi syndrome		HP:0100729	ORPHA:1545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0000324	ORPHA:2875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0000501	ORPHA:2875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0000592	ORPHA:2875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0001052	ORPHA:2875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0001053	ORPHA:2875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0001250	ORPHA:2875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0002120	ORPHA:2875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0002353	ORPHA:2875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0002514	ORPHA:2875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0003401	ORPHA:2875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0004349	ORPHA:2875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0007440	ORPHA:2875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0100026	ORPHA:2875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2875	Phakomatosis pigmentovascularis		HP:0100543	ORPHA:2875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000871	ORPHA:95512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000141	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000622	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000802	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000870	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000980	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0001278	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0001895	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0002018	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0002315	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0003158	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0007987	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0008163	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0008213	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0008214	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0008240	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0008245	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0011735	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0011748	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0012504	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0012696	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0030018	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0040171	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0040306	ORPHA:95512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000407	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000651	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0000872	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0002902	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0003493	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0004396	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0007041	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95512	Adenohypophysitis		HP:0008202	ORPHA:95512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0001256	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0001263	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0001347	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0002061	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0002064	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0002079	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0002378	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0003487	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0007020	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0009830	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0012447	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71		HP:0100022	ORPHA:401840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401840	Autosomal recessive spastic paraplegia type 71	NOT	HP:0003457	ORPHA:401840	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0002063	ORPHA:401849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0002064	ORPHA:401849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0001761	ORPHA:401849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0002839	ORPHA:401849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0002174	ORPHA:401849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0002354	ORPHA:401849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0006938	ORPHA:401849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0011446	ORPHA:401849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401849	Autosomal spastic paraplegia type 72		HP:0012531	ORPHA:401849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0002079	ORPHA:306511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0007020	ORPHA:306511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0000020	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0001249	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0001251	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0001336	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0001347	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0002061	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0002064	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0002839	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0003236	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0003319	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0007340	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0030890	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0100543	ORPHA:306511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0000488	ORPHA:306511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0001300	ORPHA:306511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0002136	ORPHA:306511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306511	Autosomal recessive spastic paraplegia type 48		HP:0009830	ORPHA:306511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2865	Short stature-webbed neck-heart disease syndrome		HP:0000465	ORPHA:2865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2865	Short stature-webbed neck-heart disease syndrome		HP:0000470	ORPHA:2865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2865	Short stature-webbed neck-heart disease syndrome		HP:0001249	ORPHA:2865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2865	Short stature-webbed neck-heart disease syndrome		HP:0001627	ORPHA:2865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2865	Short stature-webbed neck-heart disease syndrome		HP:0001999	ORPHA:2865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2865	Short stature-webbed neck-heart disease syndrome		HP:0004322	ORPHA:2865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2865	Short stature-webbed neck-heart disease syndrome		HP:0011354	ORPHA:2865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000233	ORPHA:1532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000238	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000248	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000262	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000298	ORPHA:1532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000316	ORPHA:1532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000369	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000463	ORPHA:1532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000505	ORPHA:1532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0000506	ORPHA:1532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0001251	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0001317	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0001320	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0002293	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0002342	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0002363	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0004322	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0007328	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0007957	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0011800	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0100543	ORPHA:1532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1532	Gómez-López-Hernández syndrome		HP:0100797	ORPHA:1532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0000407	ORPHA:2866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0000501	ORPHA:2866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0001363	ORPHA:2866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0002300	ORPHA:2866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0002664	ORPHA:2866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0004322	ORPHA:2866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0004397	ORPHA:2866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2866	Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome		HP:0010978	ORPHA:2866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0001510	ORPHA:2867	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0001999	ORPHA:2867	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0004322	ORPHA:2867	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0000085	ORPHA:2867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0000256	ORPHA:2867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0000308	ORPHA:2867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0000325	ORPHA:2867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0000774	ORPHA:2867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0002663	ORPHA:2867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2867	Short stature, Brussels type		HP:0100593	ORPHA:2867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0000164	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0000218	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0000508	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0000678	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0001252	ORPHA:2868	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0001634	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0001642	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0001654	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0002750	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0003498	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0004209	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0001382	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0100729	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2868	Short stature-valvular heart disease-characteristic facies syndrome		HP:0200055	ORPHA:2868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0000069	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0000366	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0001003	ORPHA:2869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0001903	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0002013	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0002027	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0002035	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0002086	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0002239	ORPHA:2869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0002664	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0002672	ORPHA:2869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0003002	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0005214	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0005244	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0005264	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0005562	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0005584	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0006725	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0008675	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0011024	ORPHA:2869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0012126	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0012720	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0012733	ORPHA:2869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0030079	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100273	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100526	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100574	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100582	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100644	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100669	ORPHA:2869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100743	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100751	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2869	Peutz-Jeghers syndrome		HP:0100833	ORPHA:2869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0000238	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0000268	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0000316	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0000347	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0000486	ORPHA:1538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0000648	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0001249	ORPHA:1538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0001305	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0001321	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0002007	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1538	Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome		HP:0005472	ORPHA:1538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000028	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000187	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000218	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000288	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000347	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000369	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000431	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000437	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000494	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000527	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000684	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0000830	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0001156	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0001257	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0001643	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0001651	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0002023	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0002645	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0004322	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0007477	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0008678	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0009804	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0012854	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0100490	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2863	Short stature-wormian bones-dextrocardia syndrome		HP:0100543	ORPHA:2863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0000708	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001250	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001252	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001254	ORPHA:156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001259	ORPHA:156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001315	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001399	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001639	ORPHA:156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001645	ORPHA:156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001939	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001943	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0001947	ORPHA:156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0002167	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0002240	ORPHA:156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0002910	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0003202	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0004374	ORPHA:156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0007185	ORPHA:156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0008279	ORPHA:156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0011675	ORPHA:156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156	Carnitine palmitoyl transferase 1A deficiency		HP:0012378	ORPHA:156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0001548	ORPHA:276280	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0004099	ORPHA:276280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0100659	ORPHA:276280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0000034	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0000105	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0001012	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0001051	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0001829	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0002624	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0002650	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0003764	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0008551	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0010714	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0012887	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0040009	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0100578	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0100585	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0100763	ORPHA:276280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276280	Hemihyperplasia-multiple lipomatosis syndrome		HP:0002667	ORPHA:276280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0000467	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0001289	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0001324	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0002013	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0002240	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0002312	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0002910	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0006846	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158	Systemic primary carnitine deficiency		HP:0007334	ORPHA:158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001324	ORPHA:157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003326	ORPHA:157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0012380	ORPHA:157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002913	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003077	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003198	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003236	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003546	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003738	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0008315	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0011936	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0040320	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0045045	ORPHA:157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001250	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001970	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002240	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002315	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002574	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003201	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003449	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003710	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0003774	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0008682	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0011964	ORPHA:157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0000113	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0000238	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0000800	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001259	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001274	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001302	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001320	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001399	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001638	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0001985	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002126	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002134	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002269	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002514	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0002643	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0006559	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0011675	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157	Carnitine palmitoyltransferase II deficiency		HP:0012443	ORPHA:157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0001644	ORPHA:154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0025169	ORPHA:154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0000969	ORPHA:154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0001635	ORPHA:154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0002875	ORPHA:154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0011675	ORPHA:154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0012378	ORPHA:154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0012764	ORPHA:154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0000407	ORPHA:154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0001727	ORPHA:154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0003198	ORPHA:154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0003457	ORPHA:154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:154	Familial isolated dilated cardiomyopathy		HP:0100578	ORPHA:154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002411	ORPHA:324442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002486	ORPHA:324442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003444	ORPHA:324442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0009053	ORPHA:324442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0100288	ORPHA:324442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001288	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001315	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001760	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002359	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003236	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003438	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003546	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003710	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0007002	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0007178	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0007289	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0012899	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0030198	ORPHA:324442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001284	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001371	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001761	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001771	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002166	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002273	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002356	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002505	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003376	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003390	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003401	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003409	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003552	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0003760	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0008944	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0008954	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0008991	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0009005	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0009027	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0009049	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0009077	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0009130	ORPHA:324442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0000975	ORPHA:324442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001171	ORPHA:324442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001256	ORPHA:324442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0001328	ORPHA:324442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0002943	ORPHA:324442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0004686	ORPHA:324442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324442	Autosomal recessive axonal neuropathy with neuromyotonia		HP:0100490	ORPHA:324442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0030429	ORPHA:289596	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0000282	ORPHA:289596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0000421	ORPHA:289596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0000520	ORPHA:289596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0000651	ORPHA:289596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0001742	ORPHA:289596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0002516	ORPHA:289596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289596	Juvenile nasopharyngeal angiofibroma		HP:0012198	ORPHA:289596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0000132	ORPHA:168816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0001824	ORPHA:168816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0002019	ORPHA:168816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0002027	ORPHA:168816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0002586	ORPHA:168816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0002664	ORPHA:168816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0003270	ORPHA:168816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0030016	ORPHA:168816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168816	Peritoneal inclusion cyst		HP:0100608	ORPHA:168816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633228	Isolated proximal femoral focal deficiency		HP:0005613	ORPHA:633228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633228	Isolated proximal femoral focal deficiency		HP:0009108	ORPHA:633228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633228	Isolated proximal femoral focal deficiency		HP:0011428	ORPHA:633228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633228	Isolated proximal femoral focal deficiency		HP:0100559	ORPHA:633228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633228	Isolated proximal femoral focal deficiency		HP:0008800	ORPHA:633228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633228	Isolated proximal femoral focal deficiency		HP:0010501	ORPHA:633228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633228	Isolated proximal femoral focal deficiency	NOT	HP:0009800	ORPHA:633228	TAS					H	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0001541	ORPHA:168811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0001824	ORPHA:168811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0001928	ORPHA:168811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0002027	ORPHA:168811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0002094	ORPHA:168811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0002586	ORPHA:168811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0002595	ORPHA:168811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0002664	ORPHA:168811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0003270	ORPHA:168811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168811	Malignant peritoneal mesothelioma		HP:0010741	ORPHA:168811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0000964	ORPHA:443811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001581	ORPHA:443811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002205	ORPHA:443811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002719	ORPHA:443811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002960	ORPHA:443811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0032218	ORPHA:443811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0031292	ORPHA:443811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0000389	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001047	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001251	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001508	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001888	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002342	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002718	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002923	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0003212	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0003237	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0004429	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0005403	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0006532	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0011343	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0031402	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0045080	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0100806	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0200029	ORPHA:443811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0000218	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0000405	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0000407	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0000793	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0000924	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001260	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001336	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001875	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001878	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001880	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001882	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001904	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001999	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002099	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002110	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002665	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002841	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0003193	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0003261	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0004430	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0004789	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0005528	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0007083	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0008587	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0011109	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0031393	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0031394	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0040148	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0040218	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0045025	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0200042	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0200101	ORPHA:443811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001156	ORPHA:443811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0001250	ORPHA:443811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002020	ORPHA:443811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0002754	ORPHA:443811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0004322	ORPHA:443811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:443811	PGM3-CDG		HP:0100633	ORPHA:443811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293621	X-linked endothelial corneal dystrophy		HP:0000585	ORPHA:293621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293621	X-linked endothelial corneal dystrophy		HP:0007663	ORPHA:293621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293621	X-linked endothelial corneal dystrophy		HP:0007957	ORPHA:293621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293621	X-linked endothelial corneal dystrophy		HP:0011488	ORPHA:293621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293621	X-linked endothelial corneal dystrophy		HP:0000565	ORPHA:293621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293621	X-linked endothelial corneal dystrophy		HP:0000639	ORPHA:293621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293621	X-linked endothelial corneal dystrophy		HP:0100018	ORPHA:293621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0100659	ORPHA:46724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0100761	ORPHA:46724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0100784	ORPHA:46724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0000505	ORPHA:46724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0001250	ORPHA:46724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0001342	ORPHA:46724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0002354	ORPHA:46724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0030746	ORPHA:46724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0100543	ORPHA:46724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:0002315	ORPHA:46724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:46724	Cerebral arteriovenous malformation		HP:5200044	ORPHA:46724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0000277	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0000716	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0001618	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0001824	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0002015	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0005216	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0010754	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0012531	ORPHA:93958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0000159	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0000273	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0000366	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0000473	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0000643	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0002487	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0003763	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0007325	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0012049	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0031008	ORPHA:93958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0001260	ORPHA:93958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0002098	ORPHA:93958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93958	Oromandibular dystonia		HP:0002451	ORPHA:93958	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001249	ORPHA:93952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002069	ORPHA:93952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0000750	ORPHA:93952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001270	ORPHA:93952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002317	ORPHA:93952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002600	ORPHA:93952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0007076	ORPHA:93952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0010819	ORPHA:93952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0012391	ORPHA:93952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0000338	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001272	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001288	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001310	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001350	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001513	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001621	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001712	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001763	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0001848	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002079	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002186	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002307	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002345	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002359	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002540	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0002650	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0003438	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0003487	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0010527	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0010529	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93952	X-linked intellectual disability, Hedera type		HP:0011812	ORPHA:93952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0000952	ORPHA:30391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001396	ORPHA:30391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001508	ORPHA:30391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001410	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001525	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0002240	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0002630	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0002908	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0002910	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0003155	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0006579	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0008151	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0011984	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0011985	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0030948	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0040321	ORPHA:30391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0000602	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0000821	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0000989	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001250	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001394	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001405	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001408	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001518	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001744	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001999	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0040075	ORPHA:30391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:30391	Isolated biliary atresia		HP:0001114	ORPHA:30391	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001396	ORPHA:53035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0000952	ORPHA:53035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001406	ORPHA:53035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002027	ORPHA:53035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002908	ORPHA:53035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0003155	ORPHA:53035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0030151	ORPHA:53035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0030948	ORPHA:53035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0000113	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0000989	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001081	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001394	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001541	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001744	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001824	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001945	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001974	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002013	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002018	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002039	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002040	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002240	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0025143	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0031964	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0032106	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0032545	ORPHA:53035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001395	ORPHA:53035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0001409	ORPHA:53035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0002613	ORPHA:53035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0030153	ORPHA:53035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease		HP:0100523	ORPHA:53035	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease	NOT	HP:0001405	ORPHA:53035	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:53035	Caroli disease	NOT	HP:0045056	ORPHA:53035	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000252	ORPHA:93950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0004325	ORPHA:93950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000248	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000327	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000582	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0001257	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0001263	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0001518	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0004322	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0008734	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0010864	ORPHA:93950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000275	ORPHA:93950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000276	ORPHA:93950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000303	ORPHA:93950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000400	ORPHA:93950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0000486	ORPHA:93950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0001256	ORPHA:93950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93950	X-linked intellectual disability, Sutherland-Haan type		HP:0002023	ORPHA:93950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:145	Hereditary breast and/or ovarian cancer syndrome		HP:0011027	ORPHA:145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:145	Hereditary breast and/or ovarian cancer syndrome		HP:0030406	ORPHA:145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:145	Hereditary breast and/or ovarian cancer syndrome		HP:0100615	ORPHA:145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:145	Hereditary breast and/or ovarian cancer syndrome		HP:0003002	ORPHA:145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:145	Hereditary breast and/or ovarian cancer syndrome		HP:0002861	ORPHA:145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:145	Hereditary breast and/or ovarian cancer syndrome		HP:0002894	ORPHA:145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:145	Hereditary breast and/or ovarian cancer syndrome		HP:0012125	ORPHA:145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001824	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002019	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002024	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002027	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002239	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0003003	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0008069	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0009720	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0012174	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0012378	ORPHA:144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0000708	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0000716	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0000737	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0000739	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001250	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001252	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001276	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001522	ORPHA:144	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002017	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002076	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002516	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0006753	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0007018	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100613	ORPHA:144	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100743	ORPHA:144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0000505	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0000738	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001123	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001260	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001288	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001371	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0001402	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002167	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002354	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002376	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002671	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002893	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002894	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0002896	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0003002	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0003006	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0003401	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0004374	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0004377	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0006725	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0006758	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0007256	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0009726	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0010524	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0010526	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0010622	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0010786	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0012114	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0012118	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100031	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100571	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100576	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100615	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100660	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100684	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0100835	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:144	Lynch syndrome		HP:0200008	ORPHA:144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:147	Carbamoyl-phosphate synthetase 1 deficiency		HP:0001250	ORPHA:147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:147	Carbamoyl-phosphate synthetase 1 deficiency		HP:0001252	ORPHA:147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:147	Carbamoyl-phosphate synthetase 1 deficiency		HP:0001951	ORPHA:147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:147	Carbamoyl-phosphate synthetase 1 deficiency		HP:0001987	ORPHA:147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:147	Carbamoyl-phosphate synthetase 1 deficiency		HP:0002093	ORPHA:147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:147	Carbamoyl-phosphate synthetase 1 deficiency		HP:0003355	ORPHA:147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:147	Carbamoyl-phosphate synthetase 1 deficiency		HP:0005961	ORPHA:147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33408	Bullous lichen planus		HP:0000989	ORPHA:33408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33408	Bullous lichen planus		HP:0008066	ORPHA:33408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33408	Bullous lichen planus		HP:0100725	ORPHA:33408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33408	Bullous lichen planus		HP:0100783	ORPHA:33408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33408	Bullous lichen planus		HP:0200034	ORPHA:33408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0001270	ORPHA:313781	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000219	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000260	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000319	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000369	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000377	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000426	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000750	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0001249	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0001250	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0001531	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0001792	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0002353	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0002421	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0002553	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0004325	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0011220	ORPHA:313781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000252	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000256	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000316	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000358	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000482	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000488	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000490	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000494	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000506	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0000664	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0001156	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0006101	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0007663	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0008589	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0010442	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0010804	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0030084	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313781	20p13 microdeletion syndrome		HP:0045025	ORPHA:313781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0000256	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0000365	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0000505	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0000618	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0000648	ORPHA:141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0000649	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0001250	ORPHA:141	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0001252	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0001263	ORPHA:141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0001276	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0001371	ORPHA:141	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0002020	ORPHA:141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0002353	ORPHA:141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0002376	ORPHA:141	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0004372	ORPHA:141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0007703	ORPHA:141	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0008872	ORPHA:141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141	Canavan disease		HP:0100543	ORPHA:141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0001395	ORPHA:33402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0002027	ORPHA:33402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0002240	ORPHA:33402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0006254	ORPHA:33402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0002013	ORPHA:33402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0002605	ORPHA:33402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0012378	ORPHA:33402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0030242	ORPHA:33402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33402	Pediatric hepatocellular carcinoma		HP:0410019	ORPHA:33402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000175	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000256	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000347	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000470	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000774	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000878	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0001601	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002093	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002650	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002757	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002779	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002786	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002827	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002982	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0003026	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0003038	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0006487	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0006584	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0008477	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0008821	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0012368	ORPHA:140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000037	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000062	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000316	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000369	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000520	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0001762	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002980	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0004322	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0010781	ORPHA:140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000126	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0000365	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002119	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0002808	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0004408	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0005280	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0007036	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140	Campomelic dysplasia		HP:0030680	ORPHA:140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0003072	ORPHA:143	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0006780	ORPHA:143	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0008200	ORPHA:143	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002148	ORPHA:143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002150	ORPHA:143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0003165	ORPHA:143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0011766	ORPHA:143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0000121	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0000131	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0000787	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0000939	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0001609	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0001824	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0001959	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002015	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0003072	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0010614	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0012232	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0012378	ORPHA:143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0000083	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0000107	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0000934	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0001324	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0001733	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002017	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002019	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002315	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002574	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002653	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0004398	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0008696	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0200025	ORPHA:143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002667	ORPHA:143	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0002890	ORPHA:143	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0006725	ORPHA:143	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0010788	ORPHA:143	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:143	Parathyroid carcinoma		HP:0012032	ORPHA:143	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0011779	ORPHA:142	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0000475	ORPHA:142	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0000853	ORPHA:142	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0001609	ORPHA:142	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0005994	ORPHA:142	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0001605	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0002015	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0002098	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0002716	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0002781	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0004894	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0012531	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0100526	ORPHA:142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0001618	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0001824	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0002094	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0002105	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0010307	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0010622	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0011805	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0012735	ORPHA:142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0002575	ORPHA:142	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:142	Anaplastic thyroid carcinoma		HP:0100836	ORPHA:142	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0031792	ORPHA:293603	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0000622	ORPHA:293603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0000639	ORPHA:293603	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0011487	ORPHA:293603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0007957	ORPHA:293603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0011490	ORPHA:293603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0012040	ORPHA:293603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0007663	ORPHA:293603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293603	Congenital hereditary endothelial dystrophy type II		HP:0000407	ORPHA:293603	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0001258	ORPHA:139480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0001347	ORPHA:139480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0002061	ORPHA:139480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0003487	ORPHA:139480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0006827	ORPHA:139480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0007002	ORPHA:139480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0009055	ORPHA:139480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0001272	ORPHA:139480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139480	Autosomal recessive spastic paraplegia type 39		HP:0002066	ORPHA:139480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001272	ORPHA:139485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0002073	ORPHA:139485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001252	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001348	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0002342	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0002376	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0003546	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0003701	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0004696	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0012752	ORPHA:139485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0000486	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001250	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001336	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001337	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001347	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0002151	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0002490	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0003128	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0003457	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0007256	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0012758	ORPHA:139485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0000365	ORPHA:139485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0000771	ORPHA:139485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139485	Autosomal recessive ataxia due to ubiquinone deficiency		HP:0001332	ORPHA:139485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0001256	ORPHA:93945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0001263	ORPHA:93945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000275	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000276	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000303	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000322	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000327	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000378	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000400	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000414	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0000486	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0002292	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0004322	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93945	X-linked intellectual disability, Porteous type		HP:0004325	ORPHA:93945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168829	Primary peritoneal carcinoma		HP:0002017	ORPHA:168829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168829	Primary peritoneal carcinoma		HP:0002019	ORPHA:168829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168829	Primary peritoneal carcinoma		HP:0002027	ORPHA:168829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168829	Primary peritoneal carcinoma		HP:0002586	ORPHA:168829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168829	Primary peritoneal carcinoma		HP:0002664	ORPHA:168829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168829	Primary peritoneal carcinoma		HP:0003270	ORPHA:168829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000160	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000175	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000252	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000272	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000347	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000378	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000414	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0000431	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0001166	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0001249	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0001263	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0001522	ORPHA:93946	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0001631	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93946	Hamel cerebro-palato-cardiac syndrome		HP:0004322	ORPHA:93946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000158	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000252	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000275	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000276	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000286	ORPHA:93947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000325	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000378	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000411	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0000582	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0001249	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0001250	ORPHA:93947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0001257	ORPHA:93947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0001264	ORPHA:93947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0001510	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0001631	ORPHA:93947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0002299	ORPHA:93947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0004322	ORPHA:93947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0008404	ORPHA:93947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93947	X-linked intellectual disability, Golabi-Ito-Hall type		HP:0011359	ORPHA:93947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0000793	ORPHA:54370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0000083	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0000093	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0000100	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0000822	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0002907	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0004746	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0005421	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0012622	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0030888	ORPHA:54370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0001919	ORPHA:54370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0003073	ORPHA:54370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0003774	ORPHA:54370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0001658	ORPHA:54370	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0001977	ORPHA:54370	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54370	Primary membranoproliferative glomerulonephritis		HP:0011510	ORPHA:54370	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000028	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000044	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000054	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000359	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000365	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000396	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000458	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000589	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000612	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000823	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001263	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001291	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000377	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0008872	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0009906	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0011382	ORPHA:138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000008	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000048	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000066	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000160	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000275	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000324	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000358	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000453	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000486	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000508	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000528	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000567	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000568	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000639	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000648	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000684	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000717	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000722	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000830	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001249	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001252	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001561	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001636	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001643	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001646	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001671	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002015	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002020	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0004322	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0005113	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0005280	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0007018	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0008897	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0010628	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0010751	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0011611	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0030680	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0100736	ORPHA:138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000076	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000085	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000126	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000175	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000204	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000252	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000286	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000316	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000384	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000478	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000504	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000625	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000632	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000772	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000834	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001156	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001305	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001360	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001511	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001537	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001601	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001883	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002093	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002410	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002553	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002575	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002650	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002937	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0002992	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0004209	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0004348	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0006824	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0007360	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0008551	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0010443	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0010669	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0010978	ORPHA:138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0000465	ORPHA:138	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0001539	ORPHA:138	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:138	CHARGE syndrome		HP:0010442	ORPHA:138	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0002093	ORPHA:93941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0003312	ORPHA:93941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0004326	ORPHA:93941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0000772	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0001601	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0001671	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0001743	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0002366	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0002575	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0002777	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0011100	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93941	Laryngotracheoesophageal cleft type 4		HP:0100016	ORPHA:93941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0012165	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0000104	ORPHA:139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0000126	ORPHA:139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0001159	ORPHA:139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0010655	ORPHA:139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0000962	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0001036	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0007431	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0008394	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0010049	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0025092	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0031517	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0045060	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0100803	ORPHA:139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0001627	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0002011	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0002089	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0002650	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0002828	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0003651	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0004552	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0009827	ORPHA:139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139	CHILD syndrome		HP:0010442	ORPHA:139	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0000164	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0000252	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0000286	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0000518	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0000944	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0000958	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0001376	ORPHA:177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0001510	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0001596	ORPHA:177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0002231	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0002650	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0003298	ORPHA:177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0004322	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0005930	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0008064	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0008905	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0009826	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0010655	ORPHA:177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0010864	ORPHA:177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:177	Rhizomelic chondrodysplasia punctata		HP:0012368	ORPHA:177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0007843	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0011508	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0030329	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0030644	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0100014	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0100533	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0100832	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0200056	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000541	ORPHA:179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0011506	ORPHA:179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0030530	ORPHA:179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000532	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000572	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000610	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0007906	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0008046	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0011505	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0011531	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0030609	ORPHA:179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000518	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000543	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000613	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179	Birdshot chorioretinopathy		HP:0000622	ORPHA:179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0002515	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0002812	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0003021	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0003025	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0006431	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0009826	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0025369	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0030299	ORPHA:174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0000907	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0001248	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0001385	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0002970	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0002980	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0003015	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0003026	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0003411	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0005028	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0005923	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0006028	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0006208	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0006634	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0008873	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0009852	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0045079	ORPHA:174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0000926	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0001513	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0002829	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0002938	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0002979	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0003301	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0003468	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0004019	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:174	Metaphyseal chondrodysplasia, Schmid type		HP:0004042	ORPHA:174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002014	ORPHA:173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001324	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001649	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001941	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001944	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002013	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002615	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002900	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002901	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002902	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0003111	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0003394	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0011036	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0011037	ORPHA:173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0000490	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0000737	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001250	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001254	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001622	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001919	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001943	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002027	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002789	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0002883	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0003128	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0005268	ORPHA:173	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0007185	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0007517	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0031274	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0032155	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0032448	ORPHA:173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001297	ORPHA:173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0001945	ORPHA:173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:173	Cholera		HP:0011951	ORPHA:173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0000962	ORPHA:254478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0007535	ORPHA:254478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0100725	ORPHA:254478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0200037	ORPHA:254478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0000989	ORPHA:254478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0011830	ORPHA:254478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0000498	ORPHA:254478	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0000509	ORPHA:254478	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0001597	ORPHA:254478	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254478	Lichen planus pemphigoides		HP:0008066	ORPHA:254478	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000545	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000774	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001315	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002024	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0003272	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0005280	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0006589	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0008155	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0011220	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000248	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000286	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000400	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000431	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000457	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000463	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000768	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000772	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000960	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001903	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002240	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002251	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002644	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002750	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0003220	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0004313	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0005616	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001382	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0008056	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0010306	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0010318	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0012722	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0100543	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0200055	ORPHA:175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000444	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000470	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000486	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000505	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000592	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000940	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000944	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001252	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001377	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001508	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001638	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001671	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001732	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0001875	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002093	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002353	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002650	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002652	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002777	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002901	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002982	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0002983	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0003027	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0003307	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0003312	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0004279	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0004625	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0005019	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0005871	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0005930	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0006487	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0007703	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0008070	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0008499	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0008873	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0008905	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0009832	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0010301	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0011849	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0045075	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0100255	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0100569	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0100729	ORPHA:175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000174	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000212	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:175	Cartilage-hair hypoplasia		HP:0000358	ORPHA:175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0000479	ORPHA:170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0000486	ORPHA:170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0000518	ORPHA:170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0000615	ORPHA:170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0002213	ORPHA:170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0002217	ORPHA:170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0002224	ORPHA:170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0002231	ORPHA:170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0002299	ORPHA:170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0005338	ORPHA:170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0005599	ORPHA:170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:170	Woolly hair		HP:0010719	ORPHA:170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0012469	ORPHA:324422	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000343	ORPHA:324422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0001290	ORPHA:324422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0002521	ORPHA:324422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000316	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000331	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000463	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000639	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000717	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000750	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0000817	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0001181	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0002283	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0002312	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0002421	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0004325	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0012443	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0030047	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324422	ALG13-CDG		HP:0100543	ORPHA:324422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0000952	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0001396	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0001508	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0001744	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0001872	ORPHA:172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0001928	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0002024	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0002240	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0002664	ORPHA:172	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0002750	ORPHA:172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0002901	ORPHA:172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0004322	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0004349	ORPHA:172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:172	Progressive familial intrahepatic cholestasis		HP:0100543	ORPHA:172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001396	ORPHA:171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0002960	ORPHA:171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0012440	ORPHA:171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001394	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001395	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001409	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001433	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001541	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001744	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001824	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001945	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0002240	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0002910	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0010638	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0012522	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0012700	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0030168	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100279	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100869	ORPHA:171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0000083	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0000716	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0000938	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0000939	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0000952	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0000989	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001081	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001402	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001635	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001733	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0002027	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0002202	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0002608	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0003073	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0003459	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0003700	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0004905	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0008151	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0011892	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0012115	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0012378	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0030153	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0040275	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100512	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100513	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100626	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100646	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100651	ORPHA:171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0000554	ORPHA:171	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0001298	ORPHA:171	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0006554	ORPHA:171	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis		HP:0100575	ORPHA:171	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis	NOT	HP:0001879	ORPHA:171	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis	NOT	HP:0005429	ORPHA:171	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis	NOT	HP:0011034	ORPHA:171	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171	Primary sclerosing cholangitis	NOT	HP:0100727	ORPHA:171	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000023	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000028	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000047	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000154	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000218	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000256	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000269	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000272	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000316	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000343	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000347	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000348	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000378	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000402	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000448	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000475	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000486	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000494	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000609	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000678	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000750	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000766	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001263	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001317	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001357	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001533	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001622	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001631	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001763	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001837	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002021	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002119	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002136	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002236	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002250	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002307	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002342	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002761	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0004322	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0004492	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0004785	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0005852	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0007370	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0008551	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0008935	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0011090	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0012471	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0012506	ORPHA:93932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000194	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000238	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000331	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000407	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000453	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000722	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000954	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0000960	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001172	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001250	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001363	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001537	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001634	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0001680	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002019	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002020	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002023	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0002092	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0005876	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0006101	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0007018	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0009762	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0012433	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93932	FG syndrome type 1		HP:0040022	ORPHA:93932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000175	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000221	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000278	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000369	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000463	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000486	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000568	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000646	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000718	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000768	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000954	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001081	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001181	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001257	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001274	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001315	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001629	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001631	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001761	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001845	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002019	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002059	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002079	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002092	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002342	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001288	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002389	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002650	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002705	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002808	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0004691	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0006101	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0006532	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0006956	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0007082	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0008499	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0009468	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0009471	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0010186	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0010557	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0011670	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0030084	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0032077	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002540	ORPHA:464738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0007413	ORPHA:464738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0011344	ORPHA:464738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000047	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000232	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000252	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000286	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000303	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000316	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000322	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000348	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000482	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000494	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000508	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000519	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001250	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001252	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0001344	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002209	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002263	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0002465	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0005274	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0010804	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0045075	ORPHA:464738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000023	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464738	Basel-Vanagaite-Smirin-Yosef syndrome		HP:0000126	ORPHA:464738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0001627	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0009813	ORPHA:294975	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0003826	ORPHA:294975	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0033127	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0000765	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0000925	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0001671	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0000271	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0000464	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0011603	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0002088	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0000175	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0000104	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0003272	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0010442	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0001159	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0001518	ORPHA:294975	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:294975	Isolated absence of upper arm and forearm with hand present		HP:0000987	ORPHA:294975	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0000010	ORPHA:93930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0000023	ORPHA:93930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0000039	ORPHA:93930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0000056	ORPHA:93930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0000069	ORPHA:93930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0000076	ORPHA:93930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0001537	ORPHA:93930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0001539	ORPHA:93930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0002566	ORPHA:93930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0002607	ORPHA:93930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0002836	ORPHA:93930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0004378	ORPHA:93930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93930	Classic bladder exstrophy		HP:0008736	ORPHA:93930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0000508	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0000657	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001251	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001256	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001257	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001272	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001310	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001321	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001332	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0001336	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002015	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002069	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002075	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002123	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002313	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002353	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002460	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0002464	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0003477	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0003693	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0007108	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0007141	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0007340	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome		HP:0008316	ORPHA:313772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0000825	ORPHA:79644	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0000707	ORPHA:79644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0001988	ORPHA:79644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0030796	ORPHA:79644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0031080	ORPHA:79644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0000845	ORPHA:79644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0001520	ORPHA:79644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0031223	ORPHA:79644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0031224	ORPHA:79644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0040299	ORPHA:79644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0001249	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0001250	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0001998	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0002104	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0003118	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0008194	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0008947	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0011968	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency		HP:0012758	ORPHA:79644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79644	Autosomal recessive hyperinsulinism due to Kir6.2 deficiency	NOT	HP:0002919	ORPHA:79644	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001010	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001881	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001922	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002718	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002719	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0012145	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0012156	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0031408	ORPHA:167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000613	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000704	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000978	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000992	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001410	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001433	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001583	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001744	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001892	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001945	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002205	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002721	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0003281	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0004527	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0005406	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0005599	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0007499	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0007663	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0007703	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0007730	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0011869	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0011990	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0012176	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0020096	ORPHA:167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000225	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000421	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000486	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000666	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000707	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000726	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000762	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000763	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000952	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000969	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0000988	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001249	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001250	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001251	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001258	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001272	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001288	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001300	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001324	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001328	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001337	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001698	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001873	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001875	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001876	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0001903	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002155	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002202	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002540	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002716	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002902	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0002910	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0003075	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0003474	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0006308	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0006824	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0006827	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0007178	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0009830	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0011900	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0012444	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0025435	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0100543	ORPHA:167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:167	Chédiak-Higashi syndrome		HP:0005585	ORPHA:167	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:169	Ringed hair disease		HP:0002213	ORPHA:169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169	Ringed hair disease		HP:0010720	ORPHA:169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168	Loose anagen syndrome		HP:0000612	ORPHA:168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168	Loose anagen syndrome		HP:0001595	ORPHA:168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168	Loose anagen syndrome		HP:0010721	ORPHA:168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163	Hereditary hyperferritinemia-cataract syndrome		HP:0000518	ORPHA:163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163	Hereditary hyperferritinemia-cataract syndrome		HP:0001939	ORPHA:163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0003236	ORPHA:280333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0006785	ORPHA:280333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0030099	ORPHA:280333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0001270	ORPHA:280333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0002317	ORPHA:280333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0002515	ORPHA:280333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0003551	ORPHA:280333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0008981	ORPHA:280333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0010864	ORPHA:280333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0001256	ORPHA:280333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0002465	ORPHA:280333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0002938	ORPHA:280333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0003391	ORPHA:280333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0003707	ORPHA:280333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280333	Alpha-dystroglycan-related limb-girdle muscular dystrophy R16		HP:0006466	ORPHA:280333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93928	Isolated epispadias		HP:0030911	ORPHA:93928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93928	Isolated epispadias		HP:0000039	ORPHA:93928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93928	Isolated epispadias		HP:0100627	ORPHA:93928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93928	Isolated epispadias		HP:0000020	ORPHA:93928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93928	Isolated epispadias		HP:0000076	ORPHA:93928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93928	Isolated epispadias		HP:0002644	ORPHA:93928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000396	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000400	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001172	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001250	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001263	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001344	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001635	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001640	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0002187	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0005781	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0006705	ORPHA:324410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000053	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000232	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000280	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000303	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000319	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000414	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0000426	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001634	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001650	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0001653	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0002465	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0002510	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0002540	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0002751	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0003376	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0004749	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0005180	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0005280	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324410	X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome		HP:0010808	ORPHA:324410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0000056	ORPHA:93929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0000070	ORPHA:93929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0000072	ORPHA:93929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0000074	ORPHA:93929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0000076	ORPHA:93929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0000085	ORPHA:93929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0000086	ORPHA:93929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0001539	ORPHA:93929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0001762	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002023	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002414	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002475	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002566	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002827	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002836	ORPHA:93929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002937	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002991	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0002992	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0008678	ORPHA:93929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0008736	ORPHA:93929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0010475	ORPHA:93929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0011027	ORPHA:93929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0011301	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93929	Cloacal exstrophy		HP:0100668	ORPHA:93929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome		HP:0001643	ORPHA:228190	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome		HP:0001647	ORPHA:228190	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome		HP:0005295	ORPHA:228190	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome		HP:0005922	ORPHA:228190	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome		HP:0004209	ORPHA:228190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome		HP:0010047	ORPHA:228190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome		HP:0011927	ORPHA:228190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228190	Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome	NOT	HP:0000271	ORPHA:228190	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0002716	ORPHA:160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0001824	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0001903	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0002027	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0002729	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0003565	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0011227	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0012378	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0025142	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0030783	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0100721	ORPHA:160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0000952	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0002017	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0003270	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0008940	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0011024	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0012735	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0025066	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0030157	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0031500	ORPHA:160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0000083	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0000790	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0001723	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0001873	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0002094	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0005214	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0006000	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0011974	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:160	Castleman disease		HP:0012050	ORPHA:160	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0002438	ORPHA:324416	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0003560	ORPHA:324416	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0007973	ORPHA:324416	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0000202	ORPHA:324416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0000238	ORPHA:324416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0002119	ORPHA:324416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0007260	ORPHA:324416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0007700	ORPHA:324416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0000078	ORPHA:324416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0004488	ORPHA:324416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0000519	ORPHA:324416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0000568	ORPHA:324416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0002085	ORPHA:324416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324416	Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome		HP:0000589	ORPHA:324416	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0000756	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0001288	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0001348	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0002063	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0002527	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0002540	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0002960	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0003394	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0025329	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0100283	ORPHA:443804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0000739	ORPHA:443804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0001387	ORPHA:443804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0031825	ORPHA:443804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:0045084	ORPHA:443804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:5000002	ORPHA:443804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:5000007	ORPHA:443804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:443804	Focal stiff limb syndrome		HP:5000012	ORPHA:443804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0100008	ORPHA:93921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0009593	ORPHA:93921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0010302	ORPHA:93921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0012531	ORPHA:93921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0000131	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0000360	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0000365	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0000518	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0001324	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0002650	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0002664	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0003401	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0012032	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0410275	ORPHA:93921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0001250	ORPHA:93921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0001621	ORPHA:93921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0002380	ORPHA:93921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0002858	ORPHA:93921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0011750	ORPHA:93921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis		HP:0033748	ORPHA:93921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93921	Full schwannomatosis	NOT	HP:0009589	ORPHA:93921	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000478	ORPHA:93926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000601	ORPHA:93926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001508	ORPHA:93926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001510	ORPHA:93926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002033	ORPHA:93926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0004322	ORPHA:93926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0011968	ORPHA:93926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000161	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000175	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000193	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000218	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000252	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000407	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000457	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000708	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000716	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000737	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000739	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000741	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001249	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001250	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001254	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001257	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001328	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001344	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002013	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002015	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002019	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002020	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002270	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002363	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002451	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002540	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002793	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002871	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0005968	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0006528	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0006979	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0007018	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0007301	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0008947	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0010654	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0011442	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0011951	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0012285	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0040327	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0045005	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0100704	ORPHA:93926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000119	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000238	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000256	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000818	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000824	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000871	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000873	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0000924	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001274	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001371	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0001627	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002465	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002650	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0002827	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0006315	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0008936	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0009914	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0009932	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0011471	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0011787	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0012718	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0012806	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0031860	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93926	Midline interhemispheric variant of holoprosencephaly		HP:0040064	ORPHA:93926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000601	ORPHA:93924	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0011968	ORPHA:93924	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000161	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000175	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000218	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000407	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000457	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000478	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000708	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000716	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000737	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000739	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000818	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000873	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001249	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001328	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001508	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001510	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002019	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002020	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002033	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002270	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002465	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0004322	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0006528	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0006979	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0007018	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0011442	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0011951	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0012285	ORPHA:93924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000119	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000193	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000238	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000252	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000256	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000741	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000824	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000871	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0000924	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001250	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001254	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001257	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001274	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001627	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002013	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002015	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002363	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002451	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002650	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002793	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002827	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002871	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0005968	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0007301	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0008947	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0008936	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0010654	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0011471	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0011787	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0012718	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0031860	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0040064	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0040327	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0100704	ORPHA:93924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001344	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0001371	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0002540	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0006315	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0009914	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0009932	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0012806	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93924	Lobar holoprosencephaly		HP:0045005	ORPHA:93924	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000478	ORPHA:93925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000601	ORPHA:93925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001508	ORPHA:93925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001510	ORPHA:93925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002033	ORPHA:93925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0004322	ORPHA:93925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0011968	ORPHA:93925	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000161	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000175	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000193	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000218	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000252	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000407	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000457	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000708	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000716	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000737	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000739	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000741	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001249	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001250	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001254	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001257	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001328	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001344	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002013	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002015	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002019	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002020	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002270	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002363	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002451	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002540	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002793	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002871	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0005968	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0006528	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0006979	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0007018	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0007301	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0008947	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0010654	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0011442	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0011951	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0012285	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0040327	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0045005	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0100704	ORPHA:93925	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000119	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000238	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000256	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000818	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000824	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000871	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000873	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0000924	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001274	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001371	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0001627	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002465	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002650	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0002827	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0006315	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0008936	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0009914	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0009932	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0011471	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0011787	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0012718	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0012806	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0031860	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93925	Alobar holoprosencephaly		HP:0040064	ORPHA:93925	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000137	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000470	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000823	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000837	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000879	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000938	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000939	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001510	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001511	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002750	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002967	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0003492	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0004322	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0006610	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0006709	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0008209	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0008222	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0008897	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0012774	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0040072	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0100625	ORPHA:99226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000218	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000278	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000347	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000365	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000369	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000403	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000465	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000474	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000475	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000708	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000739	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000758	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000786	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000822	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000869	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000872	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000914	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001328	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001397	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001513	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001531	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001800	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001952	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002162	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002705	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002808	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002857	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002910	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0005113	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0005689	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0006438	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0006456	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0007477	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0009759	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0010044	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0010047	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0010510	ORPHA:99226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000085	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000086	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000164	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000286	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000476	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000486	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000508	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000545	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000716	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000767	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000842	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000987	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000995	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001004	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001045	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001231	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001385	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001395	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001596	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001631	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001647	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001657	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001658	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001680	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001763	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001812	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001831	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002608	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002611	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002650	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002960	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0003067	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0003186	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0003764	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0004349	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0005603	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0005978	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0007018	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000377	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0009118	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0011307	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0012434	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0100646	ORPHA:99226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000150	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0000471	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0001394	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002037	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002613	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002647	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0002861	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0004383	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0004386	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0005294	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0008678	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99226	Monosomy X syndrome		HP:0012758	ORPHA:99226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001254	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001263	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001298	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001324	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001638	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001985	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001987	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0002093	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0002240	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0002615	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0002910	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0003162	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0003201	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0003215	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0003234	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0004756	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0008331	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0011675	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0045045	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0000737	ORPHA:159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0000252	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0000639	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0000961	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001250	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001259	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0001399	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0002045	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0002882	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0100520	ORPHA:159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:159	Carnitine-acylcarnitine translocase deficiency		HP:0100602	ORPHA:159	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0030067	ORPHA:370348	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0000473	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0000952	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0000989	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001250	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001265	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001541	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001733	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001824	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001892	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001903	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0001965	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0002017	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0002039	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0002315	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0002321	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0002574	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0002894	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0003270	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0003418	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0003474	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0007340	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0010302	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0010784	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0012513	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0030692	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0031030	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0031501	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0100608	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0100615	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0100711	ORPHA:370348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0000520	ORPHA:370348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0000826	ORPHA:370348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0006254	ORPHA:370348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0011932	ORPHA:370348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0025435	ORPHA:370348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370348	Peripheral primitive neuroectodermal tumor		HP:0100849	ORPHA:370348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001800	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001952	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002162	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002705	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002808	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002857	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002910	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0005113	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0005689	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0006438	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000137	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000470	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000823	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000837	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000879	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000938	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000939	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001510	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001511	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002750	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002967	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0003492	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0004322	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0006610	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0006709	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0008209	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0008222	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0008897	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0012774	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0040072	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0100625	ORPHA:99228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000218	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000278	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000347	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000365	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000369	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000403	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000465	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000474	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000475	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000708	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000739	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000758	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000786	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000822	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000869	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000872	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000914	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001328	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001397	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001513	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001531	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0006456	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0007477	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0009759	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0010044	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0010047	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0010510	ORPHA:99228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000085	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000086	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000164	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000286	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000476	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000486	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000508	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000545	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000716	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000767	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000842	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000987	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000995	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001004	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001045	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001231	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001385	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001395	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001596	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001631	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001647	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001657	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001658	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001680	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001763	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001812	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001831	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002608	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002611	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002650	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002960	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0003067	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0003186	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0003764	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0004349	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0005603	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0005978	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0007018	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000377	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0009118	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0011307	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0012434	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0100646	ORPHA:99228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000150	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0000471	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0001394	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002037	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002613	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002647	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0002861	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0004383	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0004386	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0005294	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0008678	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99228	Mosaic monosomy X syndrome		HP:0012758	ORPHA:99228	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:112	Bartter syndrome		HP:0001939	ORPHA:112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:112	Bartter syndrome		HP:0004322	ORPHA:112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:111	Barth syndrome		HP:0001644	ORPHA:111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:111	Barth syndrome		HP:0001706	ORPHA:111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:111	Barth syndrome		HP:0001874	ORPHA:111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:111	Barth syndrome		HP:0008322	ORPHA:111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0000889	ORPHA:114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0003042	ORPHA:114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0004322	ORPHA:114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0006501	ORPHA:114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0009906	ORPHA:114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0009907	ORPHA:114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0001385	ORPHA:114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0000400	ORPHA:114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0003019	ORPHA:114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:114	Auriculoosteodysplasia		HP:0005916	ORPHA:114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0002208	ORPHA:113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0001056	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0001482	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0002209	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0002671	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0003777	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0008070	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0009886	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0045075	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0200102	ORPHA:113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0000400	ORPHA:113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0000889	ORPHA:113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0001167	ORPHA:113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0100720	ORPHA:113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:113	Bazex-Dupré-Christol syndrome		HP:0100777	ORPHA:113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000556	ORPHA:110	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000548	ORPHA:110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001513	ORPHA:110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0008915	ORPHA:110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0012758	ORPHA:110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000119	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000135	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000163	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000218	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000512	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000551	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000613	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000618	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000639	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000662	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000668	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000678	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000708	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000716	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000717	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000736	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000822	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001156	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001328	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002155	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002910	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0003233	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0004322	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0004408	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0007663	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0008724	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0008736	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0012622	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0025691	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0100259	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0100543	ORPHA:110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000011	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000028	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000076	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000085	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000100	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000126	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000147	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000278	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000316	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000343	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000365	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000358	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000388	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000400	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000426	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000470	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000483	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000486	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000494	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000518	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000691	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000712	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000739	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000750	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000789	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000818	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000821	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000855	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0000858	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001159	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001249	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001250	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001251	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001257	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001382	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001395	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001397	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001627	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001762	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002099	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002167	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002230	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0003202	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0005280	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0005562	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0005978	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0006101	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0008376	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0008734	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0010747	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0011024	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0011026	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0012384	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0030010	ORPHA:110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0001638	ORPHA:110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002037	ORPHA:110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002251	ORPHA:110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0002608	ORPHA:110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:110	Bardet-Biedl syndrome		HP:0005769	ORPHA:110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228169	Autosomal dominant striatal neurodegeneration		HP:0001260	ORPHA:228169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228169	Autosomal dominant striatal neurodegeneration		HP:0001288	ORPHA:228169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228169	Autosomal dominant striatal neurodegeneration		HP:0002015	ORPHA:228169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228169	Autosomal dominant striatal neurodegeneration		HP:0002063	ORPHA:228169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228169	Autosomal dominant striatal neurodegeneration		HP:0002067	ORPHA:228169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228169	Autosomal dominant striatal neurodegeneration		HP:0002075	ORPHA:228169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228169	Autosomal dominant striatal neurodegeneration		HP:0100022	ORPHA:228169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0002480	ORPHA:529799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0003265	ORPHA:529799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0006579	ORPHA:529799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0006958	ORPHA:529799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0000407	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0000502	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0001250	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0001276	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0001343	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0001878	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0001945	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0002871	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0003073	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0011968	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0012696	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0032106	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0100021	ORPHA:529799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0003228	ORPHA:529799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0025331	ORPHA:529799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529799	Acute bilirubin encephalopathy		HP:0040187	ORPHA:529799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000256	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002250	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0003764	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0004322	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0004390	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0005306	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0007400	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0012032	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0100013	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0100026	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0100761	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0200008	ORPHA:109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000767	ORPHA:109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001482	ORPHA:109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001933	ORPHA:109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002650	ORPHA:109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000098	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000189	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000268	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000343	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000347	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000400	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000445	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000463	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000587	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000872	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0000965	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001004	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001009	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001249	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001250	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001252	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001324	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001681	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001943	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002007	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002167	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002170	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002194	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002664	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002665	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002750	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002858	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0002890	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0003196	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0003198	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0003202	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0004326	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0004942	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0001382	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0007565	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0009023	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0010784	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0011304	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:109	Bannayan-Riley-Ruvalcaba syndrome		HP:0100641	ORPHA:109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0000083	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0000613	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0000716	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0000952	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0000975	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001259	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001289	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001376	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001399	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001635	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001658	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001744	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001864	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001873	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001878	ORPHA:108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001882	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0001945	ORPHA:108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0002017	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0002039	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0002093	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0002240	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0002315	ORPHA:108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0002719	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0002829	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0003326	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0004936	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0005521	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0012378	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0012735	ORPHA:108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0100724	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:108	Babesiosis		HP:0100776	ORPHA:108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0000988	ORPHA:90000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0002829	ORPHA:90000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0003326	ORPHA:90000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0008066	ORPHA:90000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0010702	ORPHA:90000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0200029	ORPHA:90000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0200036	ORPHA:90000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90000	Erythema elevatum diutinum		HP:0200037	ORPHA:90000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0000076	ORPHA:105	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0000083	ORPHA:105	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0000010	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0000021	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0000072	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0000126	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0001562	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0003270	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0004321	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0010479	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0010955	ORPHA:105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0000110	ORPHA:105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0001541	ORPHA:105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:105	Atresia of urethra		HP:0010444	ORPHA:105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0007924	ORPHA:104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0200125	ORPHA:104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000529	ORPHA:104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000576	ORPHA:104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000603	ORPHA:104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000622	ORPHA:104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000648	ORPHA:104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0007763	ORPHA:104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0012841	ORPHA:104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000512	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000551	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0000649	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0001251	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0002174	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0003198	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0004309	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0009830	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0011675	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0020120	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:104	Leber hereditary optic neuropathy		HP:0032036	ORPHA:104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000359	ORPHA:107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000365	ORPHA:107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000370	ORPHA:107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0004467	ORPHA:107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000384	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000394	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000402	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000405	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000410	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000413	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0004452	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000377	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0008586	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0008678	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0009794	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0009796	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0011387	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0011388	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0011395	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0100272	ORPHA:107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000003	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000074	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000076	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000083	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000126	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000175	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000278	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000324	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000356	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0000407	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0007925	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0008551	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0009798	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0010628	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0011481	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0040106	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0100274	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:107	BOR syndrome		HP:0100581	ORPHA:107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90002	Undifferentiated connective tissue syndrome		HP:0020151	ORPHA:90002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90002	Undifferentiated connective tissue syndrome		HP:0034076	ORPHA:90002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90002	Undifferentiated connective tissue syndrome		HP:0034093	ORPHA:90002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0002896	ORPHA:90003	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0031140	ORPHA:90003	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0001945	ORPHA:90003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0002027	ORPHA:90003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0030057	ORPHA:90003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0000819	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0001080	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0001394	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0001824	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0002013	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0002018	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0003270	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0025406	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0410369	ORPHA:90003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0031956	ORPHA:90003	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver		HP:0031964	ORPHA:90003	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90003	Inflammatory pseudotumor of the liver	NOT	HP:0006254	ORPHA:90003	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0002075	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0002073	ORPHA:101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0000597	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0000639	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0000726	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001138	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001152	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001250	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001251	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001260	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001265	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001266	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001310	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0001336	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0002066	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0002070	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0002078	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0002345	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0004305	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0010831	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0010867	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0030890	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0100543	ORPHA:101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0000643	ORPHA:101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0002354	ORPHA:101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101	Dentatorubral pallidoluysian atrophy		HP:0012048	ORPHA:101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0000035	ORPHA:100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0000147	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0000486	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0000496	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0000639	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0000819	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0000823	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001250	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001251	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001257	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001260	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001288	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001337	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001508	ORPHA:100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0001888	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0002167	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0002205	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0002216	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0002664	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0002715	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0002721	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0002910	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0003202	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0003220	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0004313	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0004322	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0005374	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0005599	ORPHA:100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0005978	ORPHA:100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0007495	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0007565	ORPHA:100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0008065	ORPHA:100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0010515	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0100022	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0100543	ORPHA:100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0100579	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100	Ataxia-telangiectasia		HP:0100585	ORPHA:100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0000640	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0001260	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0001300	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002019	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002063	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002066	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002067	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002073	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002172	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002174	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002310	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002322	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002359	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0012332	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002494	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0002530	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0004926	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0005341	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0007256	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0008652	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0010307	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0010536	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0012658	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0012670	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0030015	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0030880	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:102	Multiple system atrophy		HP:0100595	ORPHA:102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0000822	ORPHA:280356	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0000842	ORPHA:280356	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0000877	ORPHA:280356	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0000956	ORPHA:280356	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0001397	ORPHA:280356	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0002155	ORPHA:280356	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0100578	ORPHA:280356	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0000789	ORPHA:280356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0003635	ORPHA:280356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0003758	ORPHA:280356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0008981	ORPHA:280356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0009017	ORPHA:280356	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0000147	ORPHA:280356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0000876	ORPHA:280356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0001395	ORPHA:280356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280356	PLIN1-related familial partial lipodystrophy		HP:0003117	ORPHA:280356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001010	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001249	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001250	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001252	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001263	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001328	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0002216	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0005599	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0100022	ORPHA:33445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0000545	ORPHA:33445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001337	ORPHA:33445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0000486	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0000587	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0000639	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0000648	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001251	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001257	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001276	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0001321	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0002063	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0002120	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0002205	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0002334	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0003552	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0007440	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0007754	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0008059	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0012157	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33445	Neuroectodermal melanolysosomal disease		HP:0100308	ORPHA:33445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50809	Talo-patello-scaphoid osteolysis		HP:0003037	ORPHA:50809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50809	Talo-patello-scaphoid osteolysis		HP:0006202	ORPHA:50809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50809	Talo-patello-scaphoid osteolysis		HP:0006378	ORPHA:50809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50809	Talo-patello-scaphoid osteolysis		HP:0008095	ORPHA:50809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50809	Talo-patello-scaphoid osteolysis		HP:0010044	ORPHA:50809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50809	Talo-patello-scaphoid osteolysis		HP:0100769	ORPHA:50809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001941	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001942	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001945	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002013	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002149	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002789	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002919	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0011446	ORPHA:134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0000741	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001259	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001262	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001894	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001944	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001974	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001987	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001993	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002014	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0004372	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0012735	ORPHA:134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0000713	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0000822	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0000969	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0000980	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001250	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001251	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001252	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001257	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001265	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001270	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001824	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001943	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002039	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002151	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002240	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0002615	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0003074	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0007308	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0012523	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0012705	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0500001	ORPHA:134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0001256	ORPHA:134	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:134	Beta-ketothiolase deficiency		HP:0010864	ORPHA:134	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0002795	ORPHA:133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0006516	ORPHA:133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0100326	ORPHA:133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0001824	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0002093	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0002094	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0005607	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0006527	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0012378	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0012735	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0025179	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0025393	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0025439	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0030877	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0030878	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0031392	ORPHA:133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0002206	ORPHA:133	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0100721	ORPHA:133	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:133	Chronic beryllium disease		HP:0011121	ORPHA:133	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000347	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000418	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000819	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000855	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000991	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0002155	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0002216	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0002240	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003712	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003717	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003758	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0005328	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0008065	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0009125	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0100578	ORPHA:280365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000147	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000287	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000311	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000468	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000869	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000956	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0000963	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001397	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001597	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001870	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0002621	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003233	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003292	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003635	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0004416	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0004943	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0006288	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0008968	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0008993	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0009771	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0030685	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0040266	ORPHA:280365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001635	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001639	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001677	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001733	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0001744	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0002230	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003198	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0003326	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0005115	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0005150	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0100607	ORPHA:280365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280365	Autosomal semi-dominant severe lipodystrophic laminopathy		HP:0004308	ORPHA:280365	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002352	ORPHA:136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002500	ORPHA:136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0032325	ORPHA:136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0040329	ORPHA:136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000712	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000741	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001297	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002076	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002077	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002326	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002637	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0100543	ORPHA:136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000716	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000726	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000739	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000819	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0000822	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001250	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001257	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001260	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001288	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001289	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001298	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001300	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0001342	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002015	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002140	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002170	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002301	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002333	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002354	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002463	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0007185	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0007236	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0010794	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0010992	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0012444	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0031843	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0100545	ORPHA:136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:136	Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy		HP:0002381	ORPHA:136	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0006978	ORPHA:135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0410263	ORPHA:135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000648	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000737	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001250	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001257	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001272	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001347	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002059	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002070	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002078	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002344	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0006855	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0007366	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0008209	ORPHA:135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000089	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000133	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000252	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000518	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000618	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000708	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000741	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000786	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0000869	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001260	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001264	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001269	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001270	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001298	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001310	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001371	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001433	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001510	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001511	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001558	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001562	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0001733	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002013	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002015	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002076	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002315	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0002804	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0006956	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0007361	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0008288	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0008947	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0011342	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0011968	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0012690	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0012704	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0032398	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0033049	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0100543	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0100653	ORPHA:135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:135	CACH syndrome		HP:0004481	ORPHA:135	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0000407	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0000648	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0000750	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0001260	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0001284	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0001310	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0002066	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0002073	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0002075	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0002080	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0002460	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0002828	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0003487	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0007108	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0007141	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:504476	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome		HP:0008568	ORPHA:504476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0001279	ORPHA:130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0001695	ORPHA:130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0011712	ORPHA:130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0012251	ORPHA:130	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0001649	ORPHA:130	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0001663	ORPHA:130	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0004751	ORPHA:130	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0004755	ORPHA:130	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0011704	ORPHA:130	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0011705	ORPHA:130	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0004308	ORPHA:130	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:130	Brugada syndrome		HP:0011715	ORPHA:130	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0012379	ORPHA:132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0002878	ORPHA:132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0001392	ORPHA:132	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0001635	ORPHA:132	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0001658	ORPHA:132	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0002664	ORPHA:132	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0003470	ORPHA:132	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0004887	ORPHA:132	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:132	Hereditary butyrylcholinesterase deficiency		HP:0031035	ORPHA:132	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0001409	ORPHA:131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0001541	ORPHA:131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0001744	ORPHA:131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0001394	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0001945	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002027	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002040	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002240	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002910	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0003155	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0030243	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0033045	ORPHA:131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0000083	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0000952	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0001082	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0001824	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002024	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002239	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002480	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0002586	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0005214	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0005244	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:131	Budd-Chiari syndrome		HP:0006554	ORPHA:131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0000121	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0000128	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0000729	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0001263	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0002133	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0002194	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0002197	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0002465	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0002917	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0005567	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0006872	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564178	Primary hypomagnesemia-refractory seizures-intellectual disability syndrome		HP:0012726	ORPHA:564178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0000164	ORPHA:300493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0001999	ORPHA:300493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0003165	ORPHA:300493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0004322	ORPHA:300493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0000716	ORPHA:300493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0002515	ORPHA:300493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0002814	ORPHA:300493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0005101	ORPHA:300493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0000739	ORPHA:300493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0001167	ORPHA:300493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0002007	ORPHA:300493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0002829	ORPHA:300493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300493	Sagliker syndrome		HP:0100649	ORPHA:300493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000028	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000046	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000135	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000202	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000252	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000256	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000280	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000336	ORPHA:127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000365	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000490	ORPHA:127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000508	ORPHA:127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000518	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000574	ORPHA:127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000581	ORPHA:127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000639	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0000771	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001182	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001249	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001250	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001252	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001769	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001831	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001836	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001956	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0003202	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0003272	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0004322	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0001382	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0008070	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0008734	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0008736	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0008872	ORPHA:127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0009748	ORPHA:127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:127	Borjeson-Forssman-Lehmann syndrome		HP:0009830	ORPHA:127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0000286	ORPHA:126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0000508	ORPHA:126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0000581	ORPHA:126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0005280	ORPHA:126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0000545	ORPHA:126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0011481	ORPHA:126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0000486	ORPHA:126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0000639	ORPHA:126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:126	Blepharophimosis-ptosis-epicanthus inversus syndrome		HP:0000664	ORPHA:126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0001581	ORPHA:129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0001595	ORPHA:129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0001596	ORPHA:129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0001597	ORPHA:129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0002209	ORPHA:129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0100725	ORPHA:129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0100825	ORPHA:129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0100840	ORPHA:129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:129	Pseudopelade of Brocq		HP:0200034	ORPHA:129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0000135	ORPHA:123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0001249	ORPHA:123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0000407	ORPHA:123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0001596	ORPHA:123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0002231	ORPHA:123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0002299	ORPHA:123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0003777	ORPHA:123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0100840	ORPHA:123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0000035	ORPHA:123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0000478	ORPHA:123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0002213	ORPHA:123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:123	Björnstad syndrome		HP:0008736	ORPHA:123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0001012	ORPHA:122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0002097	ORPHA:122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0002107	ORPHA:122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0002865	ORPHA:122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0002897	ORPHA:122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0005584	ORPHA:122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0007703	ORPHA:122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0010609	ORPHA:122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0100632	ORPHA:122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:122	Birt-Hogg-Dubé syndrome		HP:0200034	ORPHA:122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0001510	ORPHA:125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0001511	ORPHA:125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0001518	ORPHA:125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002715	ORPHA:125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0004313	ORPHA:125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0008850	ORPHA:125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0008887	ORPHA:125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000272	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000275	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000278	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000347	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000388	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000855	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000957	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000988	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000992	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0001010	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002020	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002664	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002719	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002720	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002850	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0003251	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0004315	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0004396	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0008209	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0031393	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0032218	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0040195	ORPHA:125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000010	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000027	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000554	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000653	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000798	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000819	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0001009	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0001029	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0001818	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002090	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002232	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002665	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002863	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0004808	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0005353	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0006510	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0006721	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0006758	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0008066	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0008069	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0011110	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0011471	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0011947	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0012384	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0012387	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0012743	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0020105	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0025615	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0031123	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0032170	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0100013	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0100273	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0100825	ORPHA:125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0000488	ORPHA:125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002667	ORPHA:125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0002878	ORPHA:125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0012126	ORPHA:125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:125	Bloom syndrome		HP:0100751	ORPHA:125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0012410	ORPHA:124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0030270	ORPHA:124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000234	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000980	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001254	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001510	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001518	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001896	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0005518	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0005532	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0011904	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0012133	ORPHA:124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000047	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000085	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000104	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000119	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000185	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000218	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000465	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000470	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000912	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001199	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001227	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001627	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001629	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001631	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001882	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001895	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0002817	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0002863	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0004322	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0009777	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0009778	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0009944	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0012758	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0020118	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0410030	ORPHA:124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000252	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000286	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000294	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000316	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000347	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000369	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000431	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000486	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000508	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0000519	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001087	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001680	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001790	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001873	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001875	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0001894	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0002669	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0004808	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0005280	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0006758	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0008551	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:124	Diamond-Blackfan anemia		HP:0040276	ORPHA:124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0004756	ORPHA:45453	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0001635	ORPHA:45453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0001695	ORPHA:45453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0006677	ORPHA:45453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0011710	ORPHA:45453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0031595	ORPHA:45453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0001557	ORPHA:45453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0004755	ORPHA:45453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0005152	ORPHA:45453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0009729	ORPHA:45453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia		HP:0001716	ORPHA:45453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45453	Incessant infant ventricular tachycardia	NOT	HP:0025169	ORPHA:45453	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0010885	ORPHA:399180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0001376	ORPHA:399180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0002653	ORPHA:399180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0002960	ORPHA:399180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0030955	ORPHA:399180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0001370	ORPHA:399180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0001288	ORPHA:399180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0002664	ORPHA:399180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0002725	ORPHA:399180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0003549	ORPHA:399180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0004377	ORPHA:399180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0031520	ORPHA:399180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399180	Secondary non-traumatic avascular necrosis		HP:0100724	ORPHA:399180	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0003115	ORPHA:45452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0004755	ORPHA:45452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0005150	ORPHA:45452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0011675	ORPHA:45452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0002789	ORPHA:45452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0004763	ORPHA:45452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0005162	ORPHA:45452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0012664	ORPHA:45452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0025074	ORPHA:45452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0001520	ORPHA:45452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0001789	ORPHA:45452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0002098	ORPHA:45452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0008872	ORPHA:45452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0009800	ORPHA:45452	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:45452	Idiopathic neonatal atrial flutter		HP:0025116	ORPHA:45452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49804	Lichen amyloidosis		HP:0000989	ORPHA:49804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49804	Lichen amyloidosis		HP:0200034	ORPHA:49804	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0001288	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0003547	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0003551	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0003698	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0003731	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0003738	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0003749	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0007126	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0007149	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0008944	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0008963	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0008994	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0009053	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0011399	ORPHA:45448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0002505	ORPHA:45448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0003326	ORPHA:45448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0008981	ORPHA:45448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0009027	ORPHA:45448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0030051	ORPHA:45448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0031108	ORPHA:45448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy		HP:0200101	ORPHA:45448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy	NOT	HP:0001626	ORPHA:45448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy	NOT	HP:0002747	ORPHA:45448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy	NOT	HP:0003552	ORPHA:45448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:45448	Miyoshi myopathy	NOT	HP:0008954	ORPHA:45448	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0001945	ORPHA:33475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002922	ORPHA:33475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0011972	ORPHA:33475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0012229	ORPHA:33475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0025258	ORPHA:33475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0031179	ORPHA:33475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000613	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000967	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000988	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002039	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002315	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002587	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0004372	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0011227	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0100806	ORPHA:33475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000083	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000236	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000365	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000737	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0000979	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0001085	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0001250	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0001254	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002329	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002516	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002615	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0003401	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0032308	ORPHA:33475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0001297	ORPHA:33475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002045	ORPHA:33475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002383	ORPHA:33475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0002643	ORPHA:33475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0006824	ORPHA:33475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0011880	ORPHA:33475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:33475	Meningococcal meningitis		HP:0031273	ORPHA:33475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0000750	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0002058	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0002136	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0001288	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0002515	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0003198	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0003236	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0003391	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0003557	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0003749	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0008981	ORPHA:119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0001638	ORPHA:119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:119	Beta-sarcoglycan-related limb-girdle muscular dystrophy R4		HP:0002913	ORPHA:119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000098	ORPHA:116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001520	ORPHA:116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002664	ORPHA:116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000105	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000112	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000121	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000154	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000158	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000269	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000280	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000303	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000363	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000520	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000776	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000842	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000995	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001052	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001139	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001513	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001528	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001537	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001539	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001561	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001582	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001622	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001738	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001943	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001998	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002150	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0003271	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0004464	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0005616	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0006267	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0008523	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0008659	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0009908	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0011417	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0011800	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0030720	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0031510	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0100555	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0100876	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000309	ORPHA:116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000023	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000028	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000073	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000076	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000150	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000175	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000219	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000239	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000260	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000329	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000362	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000787	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000821	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001540	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001639	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001640	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001744	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0001901	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002167	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002194	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002240	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002667	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002859	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002884	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0003006	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0005487	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0005562	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0006254	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0006744	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0008186	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0008676	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0008872	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0010535	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0012090	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0012758	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0030255	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0030680	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0100243	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0100589	ORPHA:116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000365	ORPHA:116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0000852	ORPHA:116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:116	Beckwith-Wiedemann syndrome		HP:0002308	ORPHA:116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0000218	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0001166	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0001371	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0001387	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0001533	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0002650	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0002803	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0002804	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0003011	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0008453	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0008544	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0009901	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0100490	ORPHA:115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0001519	ORPHA:115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0001083	ORPHA:115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0001634	ORPHA:115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0002247	ORPHA:115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0002566	ORPHA:115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0002575	ORPHA:115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0004942	ORPHA:115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:115	Congenital contractural arachnodactyly		HP:0030680	ORPHA:115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0001030	ORPHA:251393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0008066	ORPHA:251393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0002215	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0002225	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0004529	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0006297	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0008404	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0009722	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0011073	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0031045	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0032156	ORPHA:251393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0001057	ORPHA:251393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0001810	ORPHA:251393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0004552	ORPHA:251393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0008391	ORPHA:251393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0000987	ORPHA:251393	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0001056	ORPHA:251393	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0003121	ORPHA:251393	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251393	Localized junctional epidermolysis bullosa		HP:0004057	ORPHA:251393	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:118	Beta-mannosidosis		HP:0000365	ORPHA:118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:118	Beta-mannosidosis		HP:0001249	ORPHA:118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:118	Beta-mannosidosis		HP:0001250	ORPHA:118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:118	Beta-mannosidosis		HP:0001999	ORPHA:118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:118	Beta-mannosidosis		HP:0002205	ORPHA:118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:118	Beta-mannosidosis		HP:0005247	ORPHA:118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002024	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002039	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002102	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002105	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002113	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002202	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002204	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002321	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002354	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002376	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002383	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002516	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002637	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002716	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0003401	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0004420	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0006824	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0007256	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0010885	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0012819	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0033430	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000155	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000613	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001287	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001369	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001482	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001945	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002017	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002076	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002633	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0003326	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0011107	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0012378	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100796	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0200034	ORPHA:117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001061	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001269	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001288	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001289	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002027	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002239	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002315	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002638	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002829	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0003249	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0003565	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0004936	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0007813	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0008066	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0011227	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0012121	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0012219	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0012649	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0025532	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100326	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0200039	ORPHA:117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000031	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000083	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000488	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000518	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000618	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000708	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000737	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001097	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001250	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001251	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001347	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001637	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001653	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001658	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001659	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001701	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001733	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001744	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001824	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0001954	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100584	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100614	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100653	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100654	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100758	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0100820	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:4000041	ORPHA:117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0000099	ORPHA:117	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:117	Behçet disease		HP:0002014	ORPHA:117	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0001344	ORPHA:280384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0002376	ORPHA:280384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0003121	ORPHA:280384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0010864	ORPHA:280384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0000154	ORPHA:280384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0000158	ORPHA:280384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0002373	ORPHA:280384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0002987	ORPHA:280384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0006380	ORPHA:280384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0006466	ORPHA:280384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0000218	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0000322	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0000377	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0000574	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0000664	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0002015	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0002378	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0007350	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0011448	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280384	Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome		HP:0100712	ORPHA:280384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001945	ORPHA:228123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002090	ORPHA:228123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002721	ORPHA:228123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0003237	ORPHA:228123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0003496	ORPHA:228123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000707	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000987	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000988	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000989	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001369	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001880	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002098	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002105	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002113	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002716	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002922	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0003326	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0011450	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0011919	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0011921	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0011972	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012219	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012229	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012282	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012378	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012490	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012500	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012735	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0025084	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0025615	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0030351	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0032177	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0032217	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0032252	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0100721	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0100749	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0200034	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0200035	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0200149	ORPHA:228123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000014	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000077	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000083	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000119	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000238	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000365	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000479	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000613	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000622	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000751	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000818	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000885	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0000925	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001250	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001392	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001701	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001733	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001743	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001783	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0001871	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002315	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002586	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002633	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002637	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002682	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002754	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0002797	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0005916	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0010460	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0010461	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0011314	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0012864	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0020101	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0025637	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0031179	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0032161	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228123	Coccidioidomycosis		HP:0100543	ORPHA:228123	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000175	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000218	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000252	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000286	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000319	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000324	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000347	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000369	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000426	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000448	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000483	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000545	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000582	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000657	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000718	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000954	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001156	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001182	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001250	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001257	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001321	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001349	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001622	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001631	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001643	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001763	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001852	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002169	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000750	ORPHA:96148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001249	ORPHA:96148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001263	ORPHA:96148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001328	ORPHA:96148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001999	ORPHA:96148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000219	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000356	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000431	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000486	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000708	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000805	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001508	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002280	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002395	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002465	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002719	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0008897	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0008947	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0030084	ORPHA:96148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000076	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000085	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000119	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002317	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002360	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002389	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0004209	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0004322	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0005709	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0006956	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0007010	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0007018	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0007068	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0008081	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0008527	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0010743	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0011968	ORPHA:96148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000009	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000248	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000325	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000337	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000341	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000349	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000411	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000494	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000520	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000601	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000739	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0000767	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001212	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001251	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001363	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001385	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001800	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0001919	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002007	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002023	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002827	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0002938	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0003196	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0003298	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0003691	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0005487	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0008554	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96148	Distal deletion 10q syndrome		HP:0011376	ORPHA:96148	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000232	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000248	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000316	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000463	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001249	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001252	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001263	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001328	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002300	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002381	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002553	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0003196	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0005469	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0010529	ORPHA:96147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000028	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000035	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000158	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000252	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000664	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000717	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001250	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001513	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001671	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002121	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002133	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002714	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0010808	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0011097	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0011800	ORPHA:96147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000023	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000076	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000083	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000365	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000708	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000716	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000737	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000739	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0000741	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001274	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001331	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001508	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001510	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001636	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001650	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001659	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001680	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0001710	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002119	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002120	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0002360	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0008736	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0011968	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0012157	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0100308	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96147	Kleefstra syndrome due to 9q34 microdeletion		HP:0100541	ORPHA:96147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0000750	ORPHA:208513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0001260	ORPHA:208513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0001310	ORPHA:208513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0002066	ORPHA:208513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0002080	ORPHA:208513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0002194	ORPHA:208513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0010862	ORPHA:208513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0000570	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0000639	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0000657	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0001270	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0001272	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0001290	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0002075	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0006855	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0012434	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0100543	ORPHA:208513	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0001251	ORPHA:208513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0001263	ORPHA:208513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208513	Spinocerebellar ataxia type 29		HP:0025405	ORPHA:208513	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000218	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000252	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000272	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000275	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000276	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000286	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000308	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000358	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000426	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000486	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000582	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000678	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000737	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000750	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0001249	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0001250	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0001263	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0001302	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0001533	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0002126	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0002360	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0002381	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0002538	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0002751	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0002938	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0007874	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0010511	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0025406	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0100807	ORPHA:251383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000708	ORPHA:251383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000718	ORPHA:251383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0000752	ORPHA:251383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0001290	ORPHA:251383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome		HP:0001382	ORPHA:251383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251383	CK syndrome	NOT	HP:0003107	ORPHA:251383	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002194	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0012368	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000369	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0009437	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0012741	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0004904	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000113	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001611	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001999	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001513	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000248	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0009904	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002705	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000319	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001792	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000280	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000171	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001176	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001833	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0011407	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000252	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0010818	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001249	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000819	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0004322	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000752	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0007328	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0008770	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000742	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000086	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002893	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000347	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0008551	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002987	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002751	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000054	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000750	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001510	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000260	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000954	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0004691	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001643	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001655	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0005129	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0008499	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0007573	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0008513	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001531	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000506	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0009891	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000343	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000161	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0011069	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000256	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000494	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002021	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000414	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000463	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002213	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0004209	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0008081	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002032	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002247	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001734	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0005912	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002007	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0005819	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001845	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000126	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000076	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0006533	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001263	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0001290	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0002003	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0000470	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96149	Distal deletion 12q syndrome		HP:0010055	ORPHA:96149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0011904	ORPHA:251380	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0045047	ORPHA:251380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0000488	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0001744	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0001746	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0001923	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0002027	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0002113	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0002829	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0004840	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0008346	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0032169	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251380	Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome		HP:0034336	ORPHA:251380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0000708	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0000712	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0000716	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0000739	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0001328	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0002360	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0002549	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0007018	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0011458	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0030223	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0040264	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280397	Familial Alzheimer-like prion disease		HP:0100543	ORPHA:280397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000316	ORPHA:89844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001249	ORPHA:89844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001999	ORPHA:89844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0006818	ORPHA:89844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0011451	ORPHA:89844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0045028	ORPHA:89844	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000269	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000308	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000340	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000341	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000350	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000369	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000431	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000445	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001250	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001511	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0002683	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0003808	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0011344	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0011968	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0012736	ORPHA:89844	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000268	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0000479	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001181	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001272	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001274	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001631	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001655	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0001838	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0002015	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0002079	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0002098	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0002269	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0002514	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89844	Lissencephaly syndrome, Norman-Roberts type		HP:0006270	ORPHA:89844	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0000987	ORPHA:89842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001030	ORPHA:89842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001510	ORPHA:89842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001903	ORPHA:89842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0004325	ORPHA:89842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0008066	ORPHA:89842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0031903	ORPHA:89842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0000670	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001056	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001508	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001581	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0002015	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0002019	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0002020	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0002031	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0002043	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0003073	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0003202	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0003234	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0004395	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0007400	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0010450	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0011968	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0031831	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0032676	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0040303	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0100512	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0200041	ORPHA:89842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0000160	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0000572	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0000716	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0000739	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0000823	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001057	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001371	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001644	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001798	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0001802	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0002164	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0003764	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0004057	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0010296	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0011471	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0012390	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0200020	ORPHA:89842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89842	Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form		HP:0002860	ORPHA:89842	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0000989	ORPHA:89843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0008066	ORPHA:89843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0003019	ORPHA:89843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0008404	ORPHA:89843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0009811	ORPHA:89843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0012221	ORPHA:89843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0100725	ORPHA:89843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0200035	ORPHA:89843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0000152	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0000962	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0001056	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0001075	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0001482	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0002973	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0003341	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0004334	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0008388	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0100699	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0200034	ORPHA:89843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89843	Dystrophic epidermolysis bullosa pruriginosa		HP:0003212	ORPHA:89843	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0001371	ORPHA:440713	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0002804	ORPHA:440713	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0012768	ORPHA:440713	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000023	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000083	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000091	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000239	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000256	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000348	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000586	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0000601	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0001385	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0001396	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0001409	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0001540	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0001623	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0001903	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0002119	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0002570	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0002611	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0004322	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0004840	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0008850	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0011400	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0011998	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0012115	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0012157	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440713	Isolated sedoheptulokinase deficiency		HP:0100886	ORPHA:440713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0000496	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0000726	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0000743	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0001249	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0001263	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0001272	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0001300	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0001332	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0001337	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0002059	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0002063	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0002067	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0002313	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0002360	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0002448	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0002465	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0012332	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0012675	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0012678	ORPHA:329284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0000648	ORPHA:329284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0000718	ORPHA:329284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329284	Beta-propeller protein-associated neurodegeneration		HP:0001250	ORPHA:329284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0000509	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0000554	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0000708	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0000978	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0000988	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001034	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001055	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001369	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001637	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001701	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001744	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001954	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0001974	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002013	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002014	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002019	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002027	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002076	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002102	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002321	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002586	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002633	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002716	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0002829	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0003326	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0003401	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0003565	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0005214	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0006824	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0010783	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0011227	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0012733	ORPHA:32960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100537	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100539	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100614	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100658	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100749	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100776	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100781	ORPHA:32960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:32960	Tumor necrosis factor receptor 1 associated periodic syndrome		HP:0100796	ORPHA:32960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98797	Isochromosomy Yp syndrome		HP:0000027	ORPHA:98797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98797	Isochromosomy Yp syndrome		HP:0000062	ORPHA:98797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98797	Isochromosomy Yp syndrome		HP:0000771	ORPHA:98797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98797	Isochromosomy Yp syndrome		HP:0003251	ORPHA:98797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98797	Isochromosomy Yp syndrome		HP:0008193	ORPHA:98797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98797	Isochromosomy Yp syndrome		HP:0008734	ORPHA:98797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0000027	ORPHA:98798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0000062	ORPHA:98798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0000771	ORPHA:98798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0003248	ORPHA:98798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0003251	ORPHA:98798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0008193	ORPHA:98798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0008734	ORPHA:98798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98798	Isochromosomy Yq syndrome		HP:0012871	ORPHA:98798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0007874	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0008734	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0008770	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0009088	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0010627	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0011734	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0011787	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0012104	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0012105	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0012166	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0012411	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0012412	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0012650	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0025160	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0030339	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0031507	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0100716	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0100739	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0200055	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000938	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000028	ORPHA:98793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001513	ORPHA:98793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002119	ORPHA:98793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0008872	ORPHA:98793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000044	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000046	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000060	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000064	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000486	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000504	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000708	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000709	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000717	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000729	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000786	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000789	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000819	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000823	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000824	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001010	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001252	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001263	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001328	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001508	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001773	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002205	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002342	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002360	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002591	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002650	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0003241	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0004322	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0005599	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0007730	ORPHA:98793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000939	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001250	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001256	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001385	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001518	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0001558	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002578	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002714	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002870	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0002871	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0006889	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0010741	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0010829	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0031100	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0031169	ORPHA:98793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98793	Prader-Willi syndrome due to paternal 15q11q13 deletion		HP:0000826	ORPHA:98793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002353	ORPHA:98794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0004485	ORPHA:98794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0005484	ORPHA:98794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0011203	ORPHA:98794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0012758	ORPHA:98794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000154	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000486	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000687	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000729	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000736	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000748	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000752	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001010	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001513	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002019	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002033	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002079	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002167	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002307	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002395	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002650	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0004302	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0005469	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0005599	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0007730	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0008947	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0010808	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0010864	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0011968	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0012448	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0040082	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0100703	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0100738	ORPHA:98794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0000303	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001251	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001336	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001337	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001344	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002015	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002046	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002136	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002141	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0002465	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0010505	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0033063	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0040196	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0100022	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0100023	ORPHA:98794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001250	ORPHA:98794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98794	Angelman syndrome due to maternal 15q11q13 deletion		HP:0001263	ORPHA:98794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0000154	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0000687	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0001010	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0001249	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0001250	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0001263	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002353	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002395	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002465	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0005599	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0007730	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0010808	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0011968	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0100703	ORPHA:98795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0000303	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002015	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002033	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002046	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002069	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002136	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002141	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0002167	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0004485	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0005484	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0007270	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0008947	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0011185	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98795	Angelman syndrome due to paternal uniparental disomy of chromosome 15		HP:0025190	ORPHA:98795	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000028	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000047	ORPHA:98791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000218	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000252	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000272	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000278	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000286	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000316	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000337	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000347	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000348	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000358	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000431	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000470	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000494	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000768	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0000978	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0001249	ORPHA:98791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0001252	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0001371	ORPHA:98791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0001508	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0001762	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0001831	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0001935	ORPHA:98791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0002007	ORPHA:98791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0002167	ORPHA:98791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0004322	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0009891	ORPHA:98791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0009906	ORPHA:98791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0011903	ORPHA:98791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0012378	ORPHA:98791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98791	Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16		HP:0100840	ORPHA:98791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0010876	ORPHA:264675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0001531	ORPHA:264675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0002091	ORPHA:264675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0002098	ORPHA:264675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0004887	ORPHA:264675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0012418	ORPHA:264675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0025391	ORPHA:264675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0001649	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0002789	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0003651	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0011949	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0012735	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0030057	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0030830	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264675	Hereditary pulmonary alveolar proteinosis		HP:0031029	ORPHA:264675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0000962	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0000972	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001231	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0007446	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0008066	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0008388	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0200041	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0200097	ORPHA:89838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0000953	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0000989	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001010	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001056	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001075	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001508	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001802	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001807	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0001810	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0003764	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0007589	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89838	Autosomal recessive generalized epidermolysis bullosa simplex		HP:0031464	ORPHA:89838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000407	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000729	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000819	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000974	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001027	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001250	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001257	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001382	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001399	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001433	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001562	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0006129	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0010648	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0011342	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0100511	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0100633	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0410263	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001249	ORPHA:541423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001263	ORPHA:541423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001510	ORPHA:541423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001511	ORPHA:541423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0002910	ORPHA:541423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0031831	ORPHA:541423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001252	ORPHA:541423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001344	ORPHA:541423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001395	ORPHA:541423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001396	ORPHA:541423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0001397	ORPHA:541423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0002719	ORPHA:541423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0011968	ORPHA:541423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000081	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000126	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000252	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000293	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:541423	Growth delay-intellectual disability-hepatopathy syndrome		HP:0000311	ORPHA:541423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000164	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000202	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000272	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000286	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000316	ORPHA:96125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000319	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000322	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000337	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000347	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000365	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000369	ORPHA:96125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000430	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000445	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000463	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000486	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000494	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000501	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000593	ORPHA:96125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000627	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0000750	ORPHA:96125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0001256	ORPHA:96125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0001263	ORPHA:96125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0001631	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0001762	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0001773	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0002119	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0002650	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0002714	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0003422	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0004209	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0004279	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0005280	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0005930	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0007676	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0007957	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0008499	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0009918	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0011483	ORPHA:96125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96125	Distal deletion 6p syndrome		HP:0100716	ORPHA:96125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000194	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000218	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000233	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000269	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000278	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000286	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000343	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000348	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000358	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000445	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000470	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000606	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000664	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000954	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0001249	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0002858	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0004209	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0012368	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0045025	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0100008	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0100242	ORPHA:96123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000054	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000252	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0000975	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0001051	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0001072	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0001217	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0001276	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0001386	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0001433	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0004840	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0005272	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0005359	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0005781	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0006101	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0008066	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0008070	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0010541	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0010785	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96123	Monosomy 22 syndrome		HP:0100324	ORPHA:96123	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000175	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000276	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000322	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000327	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000358	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000405	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000407	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0000574	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001166	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001249	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001250	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001252	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001263	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001537	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001596	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001629	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001704	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0004313	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0001382	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0010511	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0010562	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0010882	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96129	Distal deletion 19p syndrome		HP:0100672	ORPHA:96129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0031951	ORPHA:98784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0000733	ORPHA:98784	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0002268	ORPHA:98784	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0004305	ORPHA:98784	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0000020	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0000716	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0000739	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0002883	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0011174	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0011182	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0011193	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0025236	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0031535	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0031589	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0100543	ORPHA:98784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0000708	ORPHA:98784	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0001256	ORPHA:98784	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0001345	ORPHA:98784	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0002069	ORPHA:98784	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0007018	ORPHA:98784	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98784	Sleep-related hypermotor epilepsy		HP:0025235	ORPHA:98784	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000750	ORPHA:96121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000218	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000219	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000248	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000256	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000268	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000278	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000322	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000337	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000347	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000363	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000358	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000455	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000490	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000527	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000689	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000699	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000739	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000752	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000776	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000954	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001256	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001270	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001290	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001310	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001321	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001363	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0004942	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001999	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002011	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002119	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002317	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002342	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0009879	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0009929	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0012450	ORPHA:96121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000023	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000028	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000200	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000233	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000316	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000348	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000389	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000396	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000565	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000718	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000733	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0012760	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000753	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000965	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001250	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001382	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001510	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001513	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001643	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002300	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002307	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002360	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002591	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0004322	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0004768	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0009748	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0010794	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0010864	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0011228	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0011333	ORPHA:96121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000047	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000122	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000126	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000238	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000311	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000365	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000470	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000483	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000486	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000577	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000767	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000805	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000957	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0000960	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001629	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001631	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001650	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0001763	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002779	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002937	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0002967	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0007772	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0008655	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0008684	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0012795	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0030212	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0045025	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0100716	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96121	7q11.23 microduplication syndrome		HP:0100807	ORPHA:96121	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228113	Anal fistula		HP:0005218	ORPHA:228113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228113	Anal fistula		HP:0000989	ORPHA:228113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228113	Anal fistula		HP:0100658	ORPHA:228113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228113	Anal fistula		HP:0500005	ORPHA:228113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228113	Anal fistula		HP:0001974	ORPHA:228113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228113	Anal fistula		HP:0001945	ORPHA:228113	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228113	Anal fistula		HP:0025143	ORPHA:228113	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0000975	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0001824	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0002353	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0002380	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0002411	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0003394	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0003552	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0008981	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0010546	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0100288	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:5000005	ORPHA:84142	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0002936	ORPHA:84142	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:84142	Isaacs syndrome		HP:0001324	ORPHA:84142	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0001945	ORPHA:228116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002017	ORPHA:228116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002092	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002094	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002105	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002204	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002315	ORPHA:228116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002516	ORPHA:228116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0002633	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0004936	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0004937	ORPHA:228116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0006543	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0010741	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0012378	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0012735	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0100545	ORPHA:228116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0100576	ORPHA:228116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228116	Hughes-Stovin syndrome		HP:0100749	ORPHA:228116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0020153	ORPHA:228119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0000246	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001875	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001945	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002090	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002721	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0011356	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0012203	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0020101	ORPHA:228119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001482	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001818	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001888	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002105	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002113	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002202	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0003326	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0004377	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0006516	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0025179	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0031245	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0031457	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0032177	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0032252	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0040186	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0100749	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0200034	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0200042	ORPHA:228119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0000077	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0000479	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0000491	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001369	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001392	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0001743	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002110	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002586	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0002754	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0008066	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0011450	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0012490	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0025044	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0030049	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0032156	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0033661	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0100537	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0100614	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0100658	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:228119	Fusariosis		HP:0410017	ORPHA:228119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000008	ORPHA:991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0002089	ORPHA:991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0004414	ORPHA:991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0004971	ORPHA:991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0030680	ORPHA:991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000003	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000035	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000062	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000130	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000776	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0001522	ORPHA:991	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0001539	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0004383	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0008633	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0008678	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0010458	ORPHA:991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000252	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000648	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000772	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0000889	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0001645	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0001679	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0001696	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0001743	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0002084	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0002269	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0002414	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0002435	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0004322	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0011675	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:991	PAGOD syndrome		HP:0100555	ORPHA:991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0000028	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0000175	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0000316	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0000347	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0000358	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0000476	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0001059	ORPHA:994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0001262	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0001305	ORPHA:994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0001511	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0001561	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0001989	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0002089	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0002093	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0002304	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0002375	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0002650	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0002804	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0002828	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0003700	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0005245	ORPHA:994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0005280	ORPHA:994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0010489	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:994	Fetal akinesia deformation sequence		HP:0100490	ORPHA:994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0000278	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0000486	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0000684	ORPHA:166272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0000703	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0000774	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0000926	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0000944	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0001522	ORPHA:166272	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0001643	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0002007	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0002098	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0002650	ORPHA:166272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0002673	ORPHA:166272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0002983	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0003196	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0003278	ORPHA:166272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0004279	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0004322	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0005280	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0001382	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0006487	ORPHA:166272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166272	Odontochondrodysplasia		HP:0010579	ORPHA:166272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0000160	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0000171	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0000358	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0000478	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0001274	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0001291	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0001360	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0001561	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0001696	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0002098	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0007360	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0008736	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0009914	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0009924	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0009939	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0011386	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0100596	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0100663	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:990	Agnathia-holoprosencephaly-situs inversus syndrome		HP:0100840	ORPHA:990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0008278	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0001288	ORPHA:171622	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0001256	ORPHA:171622	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0007361	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0007020	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0002395	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0001328	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0007133	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0002079	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0001761	ORPHA:171622	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0002191	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0002166	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171622	Autosomal recessive spastic paraplegia type 32		HP:0003487	ORPHA:171622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000028	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000065	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000158	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000212	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000218	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000237	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000269	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000271	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000278	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000347	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000363	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000448	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000586	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000826	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0000857	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001511	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001537	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001562	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001629	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001640	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001804	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001944	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0002123	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0002240	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0002643	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0008897	ORPHA:96191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001382	ORPHA:96191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0001643	ORPHA:96191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0010866	ORPHA:96191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96191	Paternal uniparental disomy of chromosome 6 syndrome		HP:0100767	ORPHA:96191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0000075	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0001090	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0001263	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0001290	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0001561	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0001684	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0002654	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0002751	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0004991	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0006385	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0010593	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0011327	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96190	Paternal uniparental disomy of chromosome 5 syndrome		HP:0100753	ORPHA:96190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231736	Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome		HP:0000482	ORPHA:231736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231736	Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome		HP:0000556	ORPHA:231736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231736	Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome		HP:0000567	ORPHA:231736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231736	Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome		HP:0000568	ORPHA:231736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231736	Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome		HP:0000612	ORPHA:231736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231736	Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome		HP:0007968	ORPHA:231736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231736	Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome		HP:0011502	ORPHA:231736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0002310	ORPHA:494526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0001260	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0001270	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0002072	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0002307	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0002317	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0002359	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0008936	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0011470	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0011968	ORPHA:494526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0001337	ORPHA:494526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement		HP:0100248	ORPHA:494526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494526	Infantile-onset generalized dyskinesia with orofacial involvement	NOT	HP:0012444	ORPHA:494526	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0000762	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0001288	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0001761	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002141	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002166	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0001288	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002460	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002936	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003438	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003477	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003693	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0007010	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0007141	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0008959	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0009027	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0009046	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0009130	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0010830	ORPHA:435387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0000708	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0000712	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0001260	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0001315	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0001765	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002094	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002136	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002354	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002359	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0002938	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003236	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003376	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003394	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003401	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003551	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003691	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003701	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0003731	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0006389	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0006886	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0006944	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0007328	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0008994	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0008997	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0009053	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435387	Autosomal dominant Charcot-Marie-Tooth disease type 2Y		HP:0030051	ORPHA:435387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63275	Pemphigoid gestationis		HP:0000989	ORPHA:63275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63275	Pemphigoid gestationis		HP:0001508	ORPHA:63275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63275	Pemphigoid gestationis		HP:0001511	ORPHA:63275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63275	Pemphigoid gestationis		HP:0001622	ORPHA:63275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63275	Pemphigoid gestationis		HP:0008066	ORPHA:63275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63275	Pemphigoid gestationis		HP:0200037	ORPHA:63275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0001347	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0002061	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0002064	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0002314	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0003393	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0003487	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0007020	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0001761	ORPHA:171617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0003392	ORPHA:171617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0003426	ORPHA:171617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0003427	ORPHA:171617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0003457	ORPHA:171617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0009031	ORPHA:171617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0009053	ORPHA:171617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0100561	ORPHA:171617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0002166	ORPHA:171617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0006892	ORPHA:171617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0009027	ORPHA:171617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38		HP:0100543	ORPHA:171617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38	NOT	HP:0000020	ORPHA:171617	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38	NOT	HP:0000726	ORPHA:171617	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38	NOT	HP:0001250	ORPHA:171617	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38	NOT	HP:0002921	ORPHA:171617	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38	NOT	HP:0009049	ORPHA:171617	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171617	Autosomal dominant spastic paraplegia type 38	NOT	HP:0012898	ORPHA:171617	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0031177	ORPHA:63273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0009053	ORPHA:63273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0008954	ORPHA:63273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0008959	ORPHA:63273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0009027	ORPHA:63273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0006389	ORPHA:63273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0012515	ORPHA:63273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0002141	ORPHA:63273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0030319	ORPHA:63273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0003738	ORPHA:63273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0002600	ORPHA:63273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement	NOT	HP:0002015	ORPHA:63273	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement	NOT	HP:0002747	ORPHA:63273	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0001626	ORPHA:63273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0002540	ORPHA:63273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement	NOT	HP:0003474	ORPHA:63273	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0009046	ORPHA:63273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0030200	ORPHA:63273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0001288	ORPHA:63273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0006135	ORPHA:63273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0008994	ORPHA:63273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63273	Distal myopathy with posterior leg and anterior hand involvement		HP:0001638	ORPHA:63273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002307	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002359	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0006801	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0007141	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0010544	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0040010	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0004322	ORPHA:251347	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001251	ORPHA:251347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000298	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000514	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000657	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001260	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001272	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001290	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001310	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001315	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001320	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001332	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002066	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002072	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002080	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002198	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002310	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0003438	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0100953	ORPHA:251347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000617	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000640	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000641	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000750	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0000815	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001336	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001382	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0001761	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251347	Ataxia-telangiectasia-like disorder		HP:0002075	ORPHA:251347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000160	ORPHA:989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000175	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000218	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000324	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000347	ORPHA:989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000431	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000506	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0000668	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0001156	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0001171	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0001231	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0001249	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0001291	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0001522	ORPHA:989	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0001543	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0002023	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0002167	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0005235	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0006101	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0006265	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0008872	ORPHA:989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0009776	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0009813	ORPHA:989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0009882	ORPHA:989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0010295	ORPHA:989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:989	Hypoglossia-hypodactyly syndrome		HP:0010669	ORPHA:989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:988	Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome		HP:0002991	ORPHA:988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:988	Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome		HP:0004322	ORPHA:988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:988	Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome		HP:0005048	ORPHA:988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:988	Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome		HP:0005772	ORPHA:988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:988	Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome		HP:0006443	ORPHA:988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:988	Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome		HP:0009601	ORPHA:988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0005162	ORPHA:75249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0030718	ORPHA:75249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0030950	ORPHA:75249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0031295	ORPHA:75249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0031329	ORPHA:75249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0001639	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0001653	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0002094	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0002205	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0002240	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0005110	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0005115	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0005180	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0008897	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0012398	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0012764	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0100598	ORPHA:75249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0001279	ORPHA:75249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0001297	ORPHA:75249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75249	Familial isolated restrictive cardiomyopathy		HP:0001907	ORPHA:75249	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0000268	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0000316	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0000629	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0000703	ORPHA:166277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0001376	ORPHA:166277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0001773	ORPHA:166277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0001863	ORPHA:166277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0002645	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0002756	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0003103	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0004322	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0009824	ORPHA:166277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166277	Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia		HP:0011120	ORPHA:166277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:981	Internal carotid absence		HP:0002138	ORPHA:981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:981	Internal carotid absence		HP:0002637	ORPHA:981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:981	Internal carotid absence		HP:0004944	ORPHA:981	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:981	Internal carotid absence		HP:0002315	ORPHA:981	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:981	Internal carotid absence		HP:0100702	ORPHA:981	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000826	ORPHA:96184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001252	ORPHA:96184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001270	ORPHA:96184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001773	ORPHA:96184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0008897	ORPHA:96184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0200055	ORPHA:96184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000750	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001249	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001382	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001511	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001513	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001518	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001622	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0001956	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0004322	ORPHA:96184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000028	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000160	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000175	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000193	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000218	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000293	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000322	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000347	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000403	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000445	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0000463	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0002021	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0002650	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0003124	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0004904	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0005280	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0007010	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0011220	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0011968	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96184	Temple syndrome due to maternal uniparental disomy of chromosome 14		HP:0030084	ORPHA:96184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0000276	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0000324	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0000347	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0000369	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0000470	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0000545	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0001263	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0001508	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0001511	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0001558	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0001795	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0002546	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0002751	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0002999	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0003070	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0003089	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0003468	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0011968	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0040188	ORPHA:96183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0000851	ORPHA:96183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96183	Maternal uniparental disomy of chromosome 9 syndrome		HP:0007973	ORPHA:96183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001627	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0002092	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0002205	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0003115	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0003546	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0006532	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0012417	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0031983	ORPHA:980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0000961	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001510	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001631	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001635	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001636	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001640	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001643	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001649	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001655	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001660	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001671	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0001680	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0002089	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0002094	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0002105	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0002110	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0004749	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0005110	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0006704	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0010741	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0012020	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0012664	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0012764	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0025576	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0031246	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0031664	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0040045	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0100598	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:980	Absence of the pulmonary artery		HP:0100749	ORPHA:980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0010469	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0000271	ORPHA:983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0000008	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0000022	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0000037	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0000062	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0000144	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0008633	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0008734	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0008736	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:983	Testicular regression syndrome		HP:0010468	ORPHA:983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:55654	Hypotrichosis simplex		HP:0000653	ORPHA:55654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:55654	Hypotrichosis simplex		HP:0001596	ORPHA:55654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:55654	Hypotrichosis simplex		HP:0002209	ORPHA:55654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:55654	Hypotrichosis simplex		HP:0002231	ORPHA:55654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:55654	Hypotrichosis simplex		HP:0045075	ORPHA:55654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:55654	Hypotrichosis simplex		HP:0008070	ORPHA:55654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000233	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000325	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000356	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000750	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001156	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001159	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001263	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001270	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001508	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001518	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001999	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002020	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002714	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0003162	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0004482	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0008872	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0011220	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0030084	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0100555	ORPHA:96182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000028	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000047	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000119	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000160	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000201	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000331	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000678	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000691	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000824	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000826	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000855	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000975	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001328	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001476	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001620	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001627	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002007	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002013	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002019	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002650	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002705	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002835	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002870	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0003199	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0003944	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0004209	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0004396	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0008846	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0010782	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0011094	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0012412	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0012523	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0100559	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0100633	ORPHA:96182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000085	ORPHA:96182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000110	ORPHA:96182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0000347	ORPHA:96182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0001511	ORPHA:96182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0002750	ORPHA:96182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96182	Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7		HP:0008897	ORPHA:96182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000023	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000034	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000175	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000204	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000325	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000510	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000512	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000529	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0000964	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0001249	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0001511	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0001873	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0002119	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0002721	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0003100	ORPHA:96181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0005268	ORPHA:96181	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0002194	ORPHA:96181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0002805	ORPHA:96181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0008258	ORPHA:96181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0008665	ORPHA:96181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96181	Maternal uniparental disomy of chromosome 6 syndrome		HP:0030088	ORPHA:96181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000510	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000580	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000662	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000707	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000716	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000750	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0001123	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0001249	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0001251	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0001310	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0001877	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0001927	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0002014	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0002064	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0002495	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0002600	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0002630	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0003146	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0003236	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0003563	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0003707	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0003722	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0004322	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0004325	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0004395	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0004905	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0006785	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0008181	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0008897	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0010831	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0010875	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0011892	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0011900	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0100513	ORPHA:96180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000011	ORPHA:96180	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000407	ORPHA:96180	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000648	ORPHA:96180	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0000873	ORPHA:96180	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96180	Maternal uniparental disomy of chromosome 4 syndrome		HP:0100651	ORPHA:96180	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001258	ORPHA:171629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001347	ORPHA:171629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002061	ORPHA:171629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001288	ORPHA:171629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0003487	ORPHA:171629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0009027	ORPHA:171629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0000657	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001249	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001260	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001268	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001272	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001285	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001310	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002075	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002079	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002359	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0006895	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0007325	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0007366	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0007371	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0011448	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0100543	ORPHA:171629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0000020	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0000298	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0000467	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0001250	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002120	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002454	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002607	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0002808	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0005656	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0006879	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0010677	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0011096	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0100515	ORPHA:171629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0000602	ORPHA:171629	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171629	Autosomal recessive spastic paraplegia type 35		HP:0000648	ORPHA:171629	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000164	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000271	ORPHA:978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000426	ORPHA:978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000431	ORPHA:978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000579	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000958	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000963	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0000995	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0001480	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0001596	ORPHA:978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0001597	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0001770	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0001803	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0001839	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0002209	ORPHA:978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0002213	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0002557	ORPHA:978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0002561	ORPHA:978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0003187	ORPHA:978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0006101	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0006482	ORPHA:978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0100797	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0100798	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:978	ADULT syndrome		HP:0200042	ORPHA:978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0000021	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0000079	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0000485	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0001250	ORPHA:977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0001252	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0001397	ORPHA:977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0001508	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0002242	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0002750	ORPHA:977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0003198	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0003457	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0004322	ORPHA:977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0004349	ORPHA:977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0007440	ORPHA:977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0008207	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:977	Adrenomyodystrophy		HP:0011344	ORPHA:977	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0001511	ORPHA:96179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0001560	ORPHA:96179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0008897	ORPHA:96179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0000821	ORPHA:96179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0001562	ORPHA:96179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0002643	ORPHA:96179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0003028	ORPHA:96179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0004639	ORPHA:96179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0005781	ORPHA:96179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0000041	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0000047	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0000083	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0000110	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0000546	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0000824	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0001177	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0001622	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0001763	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0002089	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0002652	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0002721	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0004209	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0004880	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0005268	ORPHA:96179	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0008209	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0008440	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0008689	ORPHA:96179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96179	Maternal uniparental disomy of chromosome 2 syndrome		HP:0001263	ORPHA:96179	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0000965	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001057	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001362	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001508	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002814	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002817	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0004050	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0008065	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0008070	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0010760	ORPHA:974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0000238	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0000486	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0000518	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0000568	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001156	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001171	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001636	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001641	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001883	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0004935	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0005916	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0006101	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0009882	ORPHA:974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001249	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001250	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001269	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001276	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001394	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001409	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001541	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001596	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001622	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001804	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001817	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001873	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0001882	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002040	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002084	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002092	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002132	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002239	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002353	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0002612	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0006970	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0010624	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:974	Adams-Oliver syndrome		HP:0100026	ORPHA:974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:973	Isolated absence/hypoplasia of fingers excluding thumb, unilateral		HP:0001799	ORPHA:973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:973	Isolated absence/hypoplasia of fingers excluding thumb, unilateral		HP:0005916	ORPHA:973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:973	Isolated absence/hypoplasia of fingers excluding thumb, unilateral		HP:0009778	ORPHA:973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:973	Isolated absence/hypoplasia of fingers excluding thumb, unilateral		HP:0009988	ORPHA:973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:973	Isolated absence/hypoplasia of fingers excluding thumb, unilateral		HP:0010049	ORPHA:973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0012379	ORPHA:976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000083	ORPHA:976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000093	ORPHA:976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000787	ORPHA:976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000822	ORPHA:976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0001919	ORPHA:976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0012622	ORPHA:976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0100518	ORPHA:976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000010	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000016	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000019	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0000791	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0003774	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0005110	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0011848	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0012587	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0030157	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:976	Adenine phosphoribosyltransferase deficiency		HP:0100520	ORPHA:976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0000846	ORPHA:75233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0001263	ORPHA:75233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0001399	ORPHA:75233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0001510	ORPHA:75233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0001541	ORPHA:75233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0001744	ORPHA:75233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0001903	ORPHA:75233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0001945	ORPHA:75233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0002017	ORPHA:75233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0002040	ORPHA:75233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0002240	ORPHA:75233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0002570	ORPHA:75233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0003270	ORPHA:75233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0004326	ORPHA:75233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0004333	ORPHA:75233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0004395	ORPHA:75233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75233	Wolman disease		HP:0010512	ORPHA:75233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001263	ORPHA:96170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000028	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000054	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000135	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000218	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000343	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000347	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000365	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000369	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000384	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000400	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000403	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000486	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000490	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000545	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000582	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000678	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000684	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000692	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000750	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000789	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001195	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001249	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001250	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001290	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001374	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001508	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001510	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001642	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001650	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001660	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002015	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002019	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002020	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002059	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002205	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002562	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002650	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002719	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002751	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0004397	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0004467	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0005815	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0009765	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0011968	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0012802	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0030820	ORPHA:96170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000023	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000089	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000122	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000175	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000193	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000238	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000252	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000483	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000508	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000540	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000776	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0000960	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001274	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001305	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001511	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001558	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001562	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001622	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001623	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001629	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001631	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0001643	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002023	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002119	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002308	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002500	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0002828	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0003028	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0005401	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0005989	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0009101	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0012714	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96170	Emanuel syndrome		HP:0012735	ORPHA:96170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000252	ORPHA:96176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0001510	ORPHA:96176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0001999	ORPHA:96176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0010864	ORPHA:96176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000047	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000048	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000054	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000062	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000316	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000400	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000431	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000463	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000832	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0002652	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0005280	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0005927	ORPHA:96176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000218	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000243	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000286	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000322	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000347	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000358	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000470	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000676	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000717	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000957	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0001000	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0001290	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0001596	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0002007	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0002023	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0002323	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0009601	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0011301	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0012211	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0030032	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0100779	ORPHA:96176	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0000479	ORPHA:96176	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0001274	ORPHA:96176	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0003256	ORPHA:96176	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0005233	ORPHA:96176	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96176	Ring chromosome 13 syndrome		HP:0009919	ORPHA:96176	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:494541	Childhood-onset benign chorea with striatal involvement		HP:0002072	ORPHA:494541	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494541	Childhood-onset benign chorea with striatal involvement		HP:0010994	ORPHA:494541	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494541	Childhood-onset benign chorea with striatal involvement		HP:0031206	ORPHA:494541	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494541	Childhood-onset benign chorea with striatal involvement		HP:0000739	ORPHA:494541	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494541	Childhood-onset benign chorea with striatal involvement		HP:0002548	ORPHA:494541	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494541	Childhood-onset benign chorea with striatal involvement	NOT	HP:0000726	ORPHA:494541	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:494541	Childhood-onset benign chorea with striatal involvement	NOT	HP:0002194	ORPHA:494541	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0000982	ORPHA:158668	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0001030	ORPHA:158668	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0008404	ORPHA:158668	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0000966	ORPHA:158668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0001508	ORPHA:158668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0002289	ORPHA:158668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0001288	ORPHA:158668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0008070	ORPHA:158668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0040181	ORPHA:158668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0040189	ORPHA:158668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0000164	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0000670	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0000989	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0001581	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0002028	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0004322	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0005218	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0006482	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0006532	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0007502	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0008066	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0012227	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0030809	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0100699	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0100806	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158668	Ectodermal dysplasia-skin fragility syndrome		HP:0100825	ORPHA:158668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000028	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000280	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000294	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000350	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000666	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001131	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0007957	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0008707	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0008729	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0011229	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0045075	ORPHA:495875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000047	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000343	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000369	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000463	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000478	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000486	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000505	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000557	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000664	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001007	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001097	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001305	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001320	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0002136	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0002172	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0002342	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0002465	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0005280	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0010864	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0011343	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0011344	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0011825	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0012110	ORPHA:495875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000064	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000107	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000252	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000347	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000455	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000470	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000527	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000609	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0000718	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001321	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001350	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0001545	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0002000	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0002020	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0006610	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0007018	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0025405	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495875	Congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome		HP:0040171	ORPHA:495875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0000763	ORPHA:658549	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0000217	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0001010	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0001097	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0007550	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0008652	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0031284	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0032147	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0033748	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0040270	ORPHA:658549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0000009	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0001962	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0002579	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0003394	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0004926	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0007328	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0010829	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0012452	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0012533	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0012700	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0033850	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:658549	Idiopathic small fibers neuropathy		HP:0100502	ORPHA:658549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440727	Combined hamartoma of the retina and retinal pigment epithelium		HP:0000577	ORPHA:440727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440727	Combined hamartoma of the retina and retinal pigment epithelium		HP:0000618	ORPHA:440727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440727	Combined hamartoma of the retina and retinal pigment epithelium		HP:0000579	ORPHA:440727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440727	Combined hamartoma of the retina and retinal pigment epithelium		HP:0007663	ORPHA:440727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440727	Combined hamartoma of the retina and retinal pigment epithelium		HP:0007773	ORPHA:440727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440727	Combined hamartoma of the retina and retinal pigment epithelium		HP:0012795	ORPHA:440727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440727	Combined hamartoma of the retina and retinal pigment epithelium		HP:0012841	ORPHA:440727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000028	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000047	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000073	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000075	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000076	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000126	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000164	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000175	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000189	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000232	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000252	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000276	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000280	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000286	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000337	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000348	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000396	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000411	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000414	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000426	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000430	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000431	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000486	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000508	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000518	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000581	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000582	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000668	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000682	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000691	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000767	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000821	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0000958	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001166	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001249	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001250	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001252	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001263	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001611	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001647	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001671	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002021	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002119	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002465	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002650	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002705	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002808	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002827	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0002948	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0003422	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0004322	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0005599	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0001382	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0007370	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0008064	ORPHA:96169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0008499	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0008872	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0009928	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0010719	ORPHA:96169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96169	Koolen-De Vries syndrome		HP:0100025	ORPHA:96169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001256	ORPHA:96168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001263	ORPHA:96168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001510	ORPHA:96168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001513	ORPHA:96168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001999	ORPHA:96168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000252	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000316	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000337	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000426	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000448	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000455	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000494	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0003256	ORPHA:96168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000286	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000347	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000358	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000363	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000421	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0000855	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001397	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001642	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001763	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0002573	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0003645	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0008151	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0010945	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0011228	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0011565	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0100608	ORPHA:96168	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001162	ORPHA:96168	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001274	ORPHA:96168	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0001830	ORPHA:96168	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0003072	ORPHA:96168	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0032152	ORPHA:96168	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96168	Monosomy 13q34 syndrome		HP:0040188	ORPHA:96168	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000028	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000164	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000316	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000347	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000463	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001249	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001263	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001582	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001595	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001869	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001999	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0002162	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0002714	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0100729	ORPHA:96167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000046	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000050	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000077	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000190	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000212	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000356	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000365	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000369	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000389	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000464	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000766	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000767	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001250	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001257	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001629	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001631	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001636	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0001643	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0002650	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0004209	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0004415	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0005280	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0006443	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0007598	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0012471	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0030680	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0100490	ORPHA:96167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000175	ORPHA:96167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000204	ORPHA:96167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000478	ORPHA:96167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0000504	ORPHA:96167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96167	Recombinant 8 syndrome		HP:0004378	ORPHA:96167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0002314	ORPHA:171612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0007020	ORPHA:171612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0001347	ORPHA:171612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0002061	ORPHA:171612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0002166	ORPHA:171612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0003487	ORPHA:171612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0007340	ORPHA:171612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0100561	ORPHA:171612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0000012	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0002064	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0002169	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0001288	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0003394	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0007350	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0001761	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37		HP:0012378	ORPHA:171612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37	NOT	HP:0001250	ORPHA:171612	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37	NOT	HP:0002921	ORPHA:171612	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37	NOT	HP:0003457	ORPHA:171612	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171612	Autosomal dominant spastic paraplegia type 37	NOT	HP:0012898	ORPHA:171612	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0008905	ORPHA:63259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0010301	ORPHA:63259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000160	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000369	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001360	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001543	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001561	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001838	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0002323	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0002414	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0003307	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0008465	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0009939	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0030680	ORPHA:63259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000078	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000104	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000202	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000238	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000476	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0000776	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001305	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001339	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001539	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0001762	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0002023	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0002084	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0002247	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0002475	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0002804	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0003396	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63259	Iniencephaly		HP:0012294	ORPHA:63259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0000407	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0000470	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0000824	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0003423	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0004322	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0008213	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0008245	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0010627	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0011748	ORPHA:231720	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231720	Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome		HP:0012287	ORPHA:231720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0001347	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0001348	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0002061	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0002166	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0002362	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0003487	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0011448	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171607	X-linked spastic paraplegia type 34		HP:0012514	ORPHA:171607	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000474	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000708	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000710	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000711	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000718	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000719	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000723	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000733	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000734	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000737	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000751	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000757	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0001268	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002145	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002354	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002371	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002381	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002442	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002465	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0006892	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0010522	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0010526	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0010529	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0030213	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0030223	ORPHA:275864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002500	ORPHA:275864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0011204	ORPHA:275864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0012658	ORPHA:275864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0030212	ORPHA:275864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000709	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0000741	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0001288	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0001347	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002069	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002071	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002300	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002380	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002446	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0002493	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275864	Behavioral variant of frontotemporal dementia		HP:0012671	ORPHA:275864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0000218	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0003458	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0003722	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0003798	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0006466	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0009005	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0009027	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0009063	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0009077	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0012036	ORPHA:399103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0001533	ORPHA:399103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0002875	ORPHA:399103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0009073	ORPHA:399103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0012548	ORPHA:399103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0030319	ORPHA:399103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:399103	Distal nebulin myopathy		HP:0001638	ORPHA:399103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0000776	ORPHA:63260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0001539	ORPHA:63260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0002023	ORPHA:63260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0002323	ORPHA:63260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0002475	ORPHA:63260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0005857	ORPHA:63260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0010301	ORPHA:63260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0010309	ORPHA:63260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63260	Craniorachischisis		HP:0010497	ORPHA:63260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000023	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000252	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000331	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000341	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000407	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000446	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000496	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000711	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000737	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001250	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001257	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001276	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001371	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001508	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0002079	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0002187	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0002650	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0003196	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0010845	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0011185	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0011471	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0011800	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0011968	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0025373	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0025405	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0100704	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0200134	ORPHA:544503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000518	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0000668	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001182	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001272	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001290	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001382	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001385	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0001999	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0002069	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0002098	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0002164	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0002750	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0005072	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0006070	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0006094	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0007514	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0011432	ORPHA:544503	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0012098	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0012448	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0012469	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0040126	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544503	RNF13-related severe early-onset epileptic encephalopathy		HP:0100806	ORPHA:544503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0000252	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0000366	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0000407	ORPHA:999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0000483	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0000613	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0000639	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0001053	ORPHA:999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0001107	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0001252	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0001256	ORPHA:999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0001770	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0004209	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0004322	ORPHA:999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0005599	ORPHA:999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0007400	ORPHA:999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:999	Ermine phenotype		HP:0007730	ORPHA:999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:998	Albinism-deafness syndrome		HP:0000407	ORPHA:998	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:998	Albinism-deafness syndrome		HP:0001053	ORPHA:998	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:998	Albinism-deafness syndrome		HP:0001100	ORPHA:998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:998	Albinism-deafness syndrome		HP:0002167	ORPHA:998	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:998	Albinism-deafness syndrome		HP:0007400	ORPHA:998	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:998	Albinism-deafness syndrome		HP:0007443	ORPHA:998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:998	Albinism-deafness syndrome		HP:0007544	ORPHA:998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0000952	ORPHA:75234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0000989	ORPHA:75234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0001394	ORPHA:75234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0001399	ORPHA:75234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0001744	ORPHA:75234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0002014	ORPHA:75234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0002017	ORPHA:75234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0002040	ORPHA:75234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0002155	ORPHA:75234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0002240	ORPHA:75234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0002634	ORPHA:75234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0003124	ORPHA:75234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75234	Cholesteryl ester storage disease		HP:0010512	ORPHA:75234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0000750	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0001284	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0001290	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0003202	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0003324	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0003390	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0003557	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0006829	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0009830	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0010994	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0011343	ORPHA:238329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0000737	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0001308	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0002093	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0002098	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0002151	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0002375	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0002376	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0002490	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0003542	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0004305	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0009025	ORPHA:238329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238329	Severe X-linked mitochondrial encephalomyopathy		HP:0008872	ORPHA:238329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0003462	ORPHA:401973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0003465	ORPHA:401973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000028	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000218	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000238	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000260	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000316	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000347	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000369	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000422	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000426	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000472	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000474	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000506	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000518	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000568	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000582	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000960	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001161	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001249	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001250	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001263	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001290	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001305	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001508	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001650	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001845	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0002079	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0002509	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0002808	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0004322	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0004691	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0005590	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0006958	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0008064	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0009941	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0010055	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0010557	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0011800	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0012433	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0100807	ORPHA:401973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000175	ORPHA:401973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000718	ORPHA:401973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0000752	ORPHA:401973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401973	MEND syndrome		HP:0001627	ORPHA:401973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000504	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000605	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000639	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000712	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000716	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000726	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000736	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000737	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000739	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000741	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000751	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0001250	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0001289	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0001324	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0001336	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0001337	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0001350	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002066	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002067	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002073	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002283	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002312	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002401	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002446	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002464	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002529	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0003487	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0005327	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0006943	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0007009	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0007017	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0007158	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0007183	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0007256	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0010846	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0011099	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0012332	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0012672	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0025152	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0100256	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0100785	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0100786	ORPHA:282166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000738	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0000746	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002072	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0002922	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0007686	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0010542	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0100292	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:282166	Inherited Creutzfeldt-Jakob disease		HP:0100661	ORPHA:282166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0001511	ORPHA:3021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0008897	ORPHA:3021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0000175	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0000218	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0000417	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0002014	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0006498	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0006501	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0009601	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0011968	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0040064	ORPHA:3021	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0004313	ORPHA:3021	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome		HP:0005403	ORPHA:3021	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome	NOT	HP:0001029	ORPHA:3021	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3021	RAPADILINO syndrome	NOT	HP:0001249	ORPHA:3021	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0000988	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0001369	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0001386	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0001945	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0002829	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0002960	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0003565	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0005681	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0011227	ORPHA:85414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0002716	ORPHA:85414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0000099	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0000938	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0001510	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0001701	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0001744	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0002027	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0002202	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0002240	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0003281	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0004890	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0012122	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85414	Systemic-onset juvenile idiopathic arthritis		HP:0033430	ORPHA:85414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0005227	ORPHA:261584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000160	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000215	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000218	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000276	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000303	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000316	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000343	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000348	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000455	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000494	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0001256	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0001891	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0002234	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0002584	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0004482	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0004783	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0007649	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0010522	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0011078	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0200040	ORPHA:261584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000347	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000470	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000954	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0001115	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0001290	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0002064	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0002162	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0003003	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0006536	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0007766	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0100245	ORPHA:261584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0000077	ORPHA:261584	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0002884	ORPHA:261584	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261584	5q22 microdeletion syndrome		HP:0100246	ORPHA:261584	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001260	ORPHA:508093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001332	ORPHA:508093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0031206	ORPHA:508093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001336	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001508	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0002015	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0002059	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0002072	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0002315	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0002530	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0008314	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0008347	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0011923	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0011968	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0012707	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0025312	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0032005	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0000639	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0000648	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001270	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001288	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0002451	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0007663	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0012179	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0100660	ORPHA:508093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0000649	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001251	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001252	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001257	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001272	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508093	MEPAN syndrome		HP:0001324	ORPHA:508093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0001369	ORPHA:85410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0003493	ORPHA:85410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0040313	ORPHA:85410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0000554	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0001382	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0001508	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0002960	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0003028	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0003565	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0005086	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0030356	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0011117	ORPHA:85410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0000572	ORPHA:85410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0000585	ORPHA:85410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0001370	ORPHA:85410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0007663	ORPHA:85410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0007833	ORPHA:85410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0008850	ORPHA:85410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0000501	ORPHA:85410	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85410	Oligoarticular juvenile idiopathic arthritis		HP:0000518	ORPHA:85410	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0000590	ORPHA:329336	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003546	ORPHA:329336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003690	ORPHA:329336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0000218	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0000365	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0001260	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0001488	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002015	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002522	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002747	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003202	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003326	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003551	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003738	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0011968	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0030196	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0030319	ORPHA:329336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0000565	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0000580	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0001638	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002076	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002141	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002361	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002406	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002505	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002549	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0002650	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003133	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0003722	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0005150	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0007141	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329336	Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		HP:0007256	ORPHA:329336	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000098	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000179	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000219	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000256	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000337	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000343	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000455	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000494	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0001520	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0001548	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0001999	ORPHA:137634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000267	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000365	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000486	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000609	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000729	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000766	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0000768	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0001256	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0001641	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0001642	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0005616	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0008058	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0011098	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0012741	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137634	Overgrowth-macrocephaly-facial dysmorphism syndrome		HP:0030680	ORPHA:137634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000707	ORPHA:356961	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000924	ORPHA:356961	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001249	ORPHA:356961	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001250	ORPHA:356961	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001263	ORPHA:356961	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002521	ORPHA:356961	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0008947	ORPHA:356961	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000252	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000478	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000951	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001155	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001272	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001531	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001999	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002086	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002500	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002540	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002650	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002715	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002910	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0004322	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0008936	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0010864	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0011968	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012345	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012348	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012363	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012448	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012469	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0025053	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0040288	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0045060	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0100704	ORPHA:356961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000407	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000474	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000486	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000577	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000826	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001010	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001285	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001363	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001511	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001627	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001762	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001840	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002059	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002079	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002673	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002686	ORPHA:356961	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0003121	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0003186	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0007366	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0007704	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0011185	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0011314	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012762	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012803	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0200012	ORPHA:356961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0000938	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001305	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001382	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0001636	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002020	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002418	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002539	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0002925	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0005736	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0006956	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0008695	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0012210	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0025484	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0025517	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0030043	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:356961	SLC35A2-CDG		HP:0100490	ORPHA:356961	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0001250	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0002354	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0002902	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0002922	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0011185	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0012756	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0020071	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0031885	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0100806	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0200149	ORPHA:163921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0000708	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0000709	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0000716	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0000739	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0001251	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0001289	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0001332	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0001336	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0011203	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0012332	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0025100	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0100022	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163921	Posttransplant acute limbic encephalitis		HP:0100543	ORPHA:163921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3023	External auditory canal atresia-vertical talus-hypertelorism syndrome		HP:0000316	ORPHA:3023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3023	External auditory canal atresia-vertical talus-hypertelorism syndrome		HP:0000365	ORPHA:3023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3023	External auditory canal atresia-vertical talus-hypertelorism syndrome		HP:0000413	ORPHA:3023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3023	External auditory canal atresia-vertical talus-hypertelorism syndrome		HP:0000486	ORPHA:3023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3023	External auditory canal atresia-vertical talus-hypertelorism syndrome		HP:0004209	ORPHA:3023	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3023	External auditory canal atresia-vertical talus-hypertelorism syndrome		HP:0007598	ORPHA:3023	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002366	ORPHA:275872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0000708	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0000716	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0000738	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0000741	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0001260	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0001300	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002015	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002071	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002073	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002171	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002186	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002273	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002314	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002385	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002442	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002460	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0003700	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0003701	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0007190	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0010549	ORPHA:275872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0000605	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0000734	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0001265	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0001283	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002283	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002300	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002380	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0003487	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0008322	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0008619	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0030223	ORPHA:275872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0000508	ORPHA:275872	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002127	ORPHA:275872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275872	Frontotemporal dementia with motor neuron disease		HP:0002145	ORPHA:275872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0002607	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0002644	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0003199	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0005640	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0008479	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0008517	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0009800	ORPHA:3027	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0011867	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0100710	ORPHA:3027	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000069	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000073	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000076	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000086	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000104	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0001315	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0001387	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0001762	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0002023	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0002650	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0030680	ORPHA:3027	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000028	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000062	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000083	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000202	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000822	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0000921	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0002089	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0002139	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3027	Caudal regression syndrome		HP:0002308	ORPHA:3027	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0009027	ORPHA:59135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0011916	ORPHA:59135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0000218	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0000467	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0001288	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0001430	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0002460	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0002650	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0003323	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0003326	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0003789	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0003803	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0004696	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0008180	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0008316	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0012507	ORPHA:59135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0001644	ORPHA:59135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0003458	ORPHA:59135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy		HP:0008994	ORPHA:59135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59135	Laing distal myopathy	NOT	HP:0003805	ORPHA:59135	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001999	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0011911	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0011800	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001363	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000248	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000262	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001760	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001155	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001166	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0030084	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0012385	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001440	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0009701	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003019	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001838	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001883	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002974	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003041	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0005892	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0008368	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000062	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000811	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000055	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0040253	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0025486	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000032	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000047	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000054	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003154	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0008163	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031074	ORPHA:95699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031213	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031216	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031187	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031215	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0030349	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031083	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000822	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000028	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000786	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0008675	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000823	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000798	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000144	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0008072	ORPHA:95699	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001007	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000924	ORPHA:95699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003070	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001377	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002987	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0006487	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002980	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0011302	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001371	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001762	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000772	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003468	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000882	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002650	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000774	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003275	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0006439	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003049	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001519	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0005913	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002967	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0010049	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0006118	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002007	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000260	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000452	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000453	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000414	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003196	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0005280	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000160	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002705	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000377	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000369	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000402	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000405	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000238	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000079	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0010946	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000076	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000122	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002020	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002019	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001545	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0011403	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0002308	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0007466	ORPHA:95699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000750	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0010862	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0003826	ORPHA:95699	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000927	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0009738	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000363	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001376	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0001156	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0032362	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0011969	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0008232	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0008214	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031100	ORPHA:95699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0008221	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0031065	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95699	Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency		HP:0000147	ORPHA:95699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000175	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000201	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000252	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000316	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000430	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001156	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001256	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001263	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0002263	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0011341	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0012745	ORPHA:364577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000171	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000232	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000365	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000385	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000414	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000426	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000506	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000568	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000639	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000664	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000677	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000957	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0000996	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001252	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001508	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001511	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001562	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0001792	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0002000	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0003196	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0005487	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0006289	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0007957	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0009246	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0010752	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0010804	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0011078	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0011401	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0012370	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0030680	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0045074	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364577	Intellectual disability-brachydactyly-Pierre Robin syndrome		HP:0100380	ORPHA:364577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001369	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001386	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001387	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001785	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0002829	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0003019	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0003565	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0005086	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0005186	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0100686	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0100769	ORPHA:85408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0000554	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001155	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001371	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001384	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001530	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001824	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001832	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001903	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0002716	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0003043	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0003319	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0003326	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0003493	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0008843	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0010754	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0011134	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0011911	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0040313	ORPHA:85408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001094	ORPHA:85408	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85408	Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis		HP:0001433	ORPHA:85408	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0001263	ORPHA:401986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0002119	ORPHA:401986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0007370	ORPHA:401986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0000079	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0000256	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0000722	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0001249	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0001250	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0001252	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0002007	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0002144	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0007018	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0007099	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0030746	ORPHA:401986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0000965	ORPHA:401986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0001363	ORPHA:401986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0007906	ORPHA:401986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401986	1p31p32 microdeletion syndrome		HP:0011834	ORPHA:401986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000194	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000252	ORPHA:52503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000272	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000298	ORPHA:52503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000508	ORPHA:52503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000729	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000742	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000750	ORPHA:52503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001249	ORPHA:52503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001250	ORPHA:52503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001251	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001252	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001263	ORPHA:52503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001276	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001332	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0002019	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0002072	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0000752	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001582	ORPHA:52503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0002251	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0002305	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0002595	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0004322	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0004326	ORPHA:52503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0001382	ORPHA:52503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52503	X-linked creatine transporter deficiency		HP:0012113	ORPHA:52503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0001216	ORPHA:3010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0002353	ORPHA:3010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0008947	ORPHA:3010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0011344	ORPHA:3010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0012450	ORPHA:3010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0200000	ORPHA:3010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000028	ORPHA:3010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0001182	ORPHA:3010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0001250	ORPHA:3010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0002719	ORPHA:3010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000194	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000289	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000316	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000426	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000473	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000486	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000685	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0000767	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0001792	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0002307	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0002705	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0003270	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3010	Qazi-Markouizos syndrome		HP:0007477	ORPHA:3010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000293	ORPHA:513456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000687	ORPHA:513456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000750	ORPHA:513456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001249	ORPHA:513456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001250	ORPHA:513456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0010803	ORPHA:513456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0430028	ORPHA:513456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000168	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000280	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000347	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000463	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001252	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001508	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002069	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002121	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0005274	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0005280	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0005338	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0007800	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0008872	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0010800	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0011342	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0011344	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0025336	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0031936	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0410263	ORPHA:513456	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000175	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000252	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000403	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000486	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000540	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000545	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000646	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000729	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0000733	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001302	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001321	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001344	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001385	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001629	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001761	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0001840	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002019	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002020	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002066	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002079	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002119	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002136	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002373	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0002779	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0005750	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0006808	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0006897	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0008762	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0010740	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0011471	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0011842	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0012020	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0012172	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0012683	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0025186	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome		HP:0040115	ORPHA:513456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001250	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001257	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001332	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001336	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001338	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002015	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002020	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002119	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002120	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002650	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0007096	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0008936	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0011344	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0011451	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0011471	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0012110	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0030890	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0100704	ORPHA:500144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0000011	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0000648	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001274	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001561	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0001605	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002376	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002490	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0002521	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0005484	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0011097	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0012796	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500144	Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome		HP:0030043	ORPHA:500144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0000298	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0000741	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0001260	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0001300	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002063	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002067	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002120	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002167	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002172	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002322	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002362	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002425	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002527	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0002987	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0004673	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0007034	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0007311	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0007975	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0011121	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306692	Cyanide-induced parkinsonism-dystonia		HP:0012157	ORPHA:306692	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0000020	ORPHA:329329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0000750	ORPHA:329329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0001252	ORPHA:329329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0001263	ORPHA:329329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0001302	ORPHA:329329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0001315	ORPHA:329329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0002069	ORPHA:329329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0000316	ORPHA:329329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0000506	ORPHA:329329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0000565	ORPHA:329329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329329	Autosomal recessive frontotemporal pachygyria		HP:0001250	ORPHA:329329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000169	ORPHA:3019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000189	ORPHA:3019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000293	ORPHA:3019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000405	ORPHA:3019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000407	ORPHA:3019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000593	ORPHA:3019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000682	ORPHA:3019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000684	ORPHA:3019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000819	ORPHA:3019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0000962	ORPHA:3019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0001249	ORPHA:3019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0001250	ORPHA:3019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0001508	ORPHA:3019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0002230	ORPHA:3019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0002797	ORPHA:3019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0007703	ORPHA:3019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3019	Ramon syndrome		HP:0100585	ORPHA:3019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0001332	ORPHA:352596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0001336	ORPHA:352596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002788	ORPHA:352596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0007256	ORPHA:352596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0000252	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0001326	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002123	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002133	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002188	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002376	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0008935	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0011968	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0200134	ORPHA:352596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0001262	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0001263	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0001269	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002071	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002301	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0002506	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0025152	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0100275	ORPHA:352596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352596	Progressive myoclonic epilepsy with dystonia		HP:0000648	ORPHA:352596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000233	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000293	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000311	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000414	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000750	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0001250	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0001270	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002003	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002015	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002164	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002999	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0008936	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0010864	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0011822	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0200005	ORPHA:495818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000160	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000252	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000421	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000483	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000486	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000506	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000708	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0001357	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0001762	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002019	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002099	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002540	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002553	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0003065	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0005487	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0006471	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0010665	ORPHA:495818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000028	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000046	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000054	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000077	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000248	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000369	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000377	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000445	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000465	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000470	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0000954	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0001009	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0001285	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0001643	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002188	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0002518	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0006443	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0006855	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0010720	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0011825	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495818	9q33.3q34.11 microdeletion syndrome		HP:0100633	ORPHA:495818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0000491	ORPHA:163934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0000958	ORPHA:163934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0001097	ORPHA:163934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0007957	ORPHA:163934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0000492	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0000498	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0000613	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0000622	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0007879	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0011457	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0011496	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0030953	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0200026	ORPHA:163934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0000559	ORPHA:163934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163934	Atopic keratoconjunctivitis		HP:0012375	ORPHA:163934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3011	Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome		HP:0000510	ORPHA:3011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3011	Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome		HP:0001141	ORPHA:3011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3011	Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome		HP:0002187	ORPHA:3011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3011	Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome		HP:0002376	ORPHA:3011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3011	Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome		HP:0008610	ORPHA:3011	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000003	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000104	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000110	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000278	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000347	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000444	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000470	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0000772	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0001156	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002094	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002098	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002202	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002705	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002714	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002878	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002983	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0002984	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0003312	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0003510	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0004279	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0005280	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0008678	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0009811	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3015	Radio-renal syndrome		HP:0010310	ORPHA:3015	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0000238	ORPHA:3016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0001562	ORPHA:3016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0002984	ORPHA:3016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0012165	ORPHA:3016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0100257	ORPHA:3016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0000143	ORPHA:3016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0002023	ORPHA:3016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0004871	ORPHA:3016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3016	Absent radius-anogenital anomalies syndrome		HP:0025023	ORPHA:3016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000316	ORPHA:247262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001250	ORPHA:247262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001263	ORPHA:247262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0003155	ORPHA:247262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0006118	ORPHA:247262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0008947	ORPHA:247262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000431	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000637	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001249	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001510	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001999	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002069	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002714	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0010804	ORPHA:247262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000126	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000193	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000218	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000248	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000280	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000286	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000289	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000303	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000311	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000322	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000347	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000378	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000391	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000414	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000426	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000470	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000540	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000565	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000582	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000594	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000657	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000729	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0000767	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001009	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001195	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001251	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001288	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001315	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001336	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001357	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001385	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001545	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001562	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0001792	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002251	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002342	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002392	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002553	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002558	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002650	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0002696	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0006808	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0010850	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0010864	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0011471	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0030084	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0040194	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247262	Hyperphosphatasia-intellectual disability syndrome		HP:0040195	ORPHA:247262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000712	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0001276	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0001288	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0001332	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002067	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002071	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002172	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002174	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002315	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002354	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002396	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002453	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0003287	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0006979	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0025464	ORPHA:306682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000505	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000718	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000722	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000746	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000748	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000802	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0001289	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0002304	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0030018	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0040306	ORPHA:306682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000716	ORPHA:306682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000737	ORPHA:306682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0000738	ORPHA:306682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:5200321	ORPHA:306682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306682	Manganese poisoning		HP:0031466	ORPHA:306682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0000708	ORPHA:306686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0002354	ORPHA:306686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0002518	ORPHA:306686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0012706	ORPHA:306686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0012708	ORPHA:306686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0002063	ORPHA:306686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0002067	ORPHA:306686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0002817	ORPHA:306686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306686	Delayed encephalopathy due to carbon monoxide poisoning		HP:0004673	ORPHA:306686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0007256	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0011169	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012448	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012469	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012698	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012762	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0025160	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0025336	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0030051	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0030890	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0100660	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001259	ORPHA:3008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0100023	ORPHA:3008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002151	ORPHA:3008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003128	ORPHA:3008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0032653	ORPHA:3008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001250	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001508	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001510	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001942	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001987	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002161	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002490	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003348	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003542	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003648	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0008358	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0011966	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012644	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012706	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012707	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012708	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0012758	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0410175	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500147	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500149	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500181	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500198	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500200	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500231	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500233	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0500246	ORPHA:3008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0000639	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0000722	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0000741	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0000817	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001249	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001251	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001252	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001262	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001274	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001290	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001332	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001337	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001943	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0001944	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002013	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002039	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002119	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002240	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002416	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002465	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002789	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0002793	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003074	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003228	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003265	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0003429	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0006999	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3008	Pyruvate carboxylase deficiency		HP:0007109	ORPHA:3008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0000590	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0001488	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0002015	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0003325	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0003390	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0003797	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0007340	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0008615	ORPHA:329314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0000486	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0000518	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0000648	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0000716	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0000726	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0001251	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0001618	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0003326	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0003394	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0003558	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0003749	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0025406	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency		HP:0100543	ORPHA:329314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0000040	ORPHA:3000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0000053	ORPHA:3000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0000098	ORPHA:3000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0000708	ORPHA:3000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0000798	ORPHA:3000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0000826	ORPHA:3000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0001061	ORPHA:3000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0001595	ORPHA:3000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0003251	ORPHA:3000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0005616	ORPHA:3000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3000	Familial peripheral male-limited precocious puberty		HP:0007018	ORPHA:3000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0001873	ORPHA:3002	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0000967	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0000979	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0004420	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0025329	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0025379	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0030908	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0032069	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0034062	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0034063	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0034189	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:4000170	ORPHA:3002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0000225	ORPHA:3002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0000421	ORPHA:3002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0000790	ORPHA:3002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0000978	ORPHA:3002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0002239	ORPHA:3002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0034263	ORPHA:3002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0001342	ORPHA:3002	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3002	Immune thrombocytopenia		HP:0011885	ORPHA:3002	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0000369	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0000457	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0000465	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0000773	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0000888	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0002694	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0002983	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0003026	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0003175	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0003270	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0004493	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0008817	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0010306	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0011338	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0011867	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0012790	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0030290	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0040194	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0100540	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0100625	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0100748	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0100856	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3003	Pyknoachondrogenesis		HP:0100866	ORPHA:3003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3004	Mirror polydactyly-vertebral segmentation-limbs defects syndrome		HP:0001171	ORPHA:3004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3004	Mirror polydactyly-vertebral segmentation-limbs defects syndrome		HP:0001829	ORPHA:3004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3004	Mirror polydactyly-vertebral segmentation-limbs defects syndrome		HP:0002247	ORPHA:3004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3004	Mirror polydactyly-vertebral segmentation-limbs defects syndrome		HP:0003422	ORPHA:3004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3004	Mirror polydactyly-vertebral segmentation-limbs defects syndrome		HP:0004322	ORPHA:3004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3004	Mirror polydactyly-vertebral segmentation-limbs defects syndrome		HP:0005359	ORPHA:3004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3004	Mirror polydactyly-vertebral segmentation-limbs defects syndrome		HP:0009829	ORPHA:3004	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0002857	ORPHA:3005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0004975	ORPHA:3005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0000303	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0000411	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0000670	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0000689	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0002659	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0003051	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0005464	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0006599	ORPHA:3005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0000696	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0000926	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0001324	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0002645	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0002650	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0002829	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0003418	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3005	Pyle disease		HP:0010539	ORPHA:3005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0003128	ORPHA:3006	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0001250	ORPHA:3006	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0000737	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0001557	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0002079	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0002133	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0002643	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0007359	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0010845	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0010851	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0011152	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0011968	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0012758	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0020217	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0025116	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0030917	ORPHA:3006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0000273	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0000496	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0000711	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0001249	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0002119	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0002188	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0002280	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0002521	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0010819	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0010841	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0011097	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0011166	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0011198	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0011199	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0012420	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0012444	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0012704	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0012768	ORPHA:3006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3006	Pyridoxine-dependent-developmental and epileptic encephalopathy		HP:0001943	ORPHA:3006	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0000738	ORPHA:513436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0007153	ORPHA:513436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78	NOT	HP:0003202	ORPHA:513436	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0000486	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0001260	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0001272	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0001347	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0002073	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0002120	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0001288	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0003477	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0003482	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0003487	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0007020	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0007240	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0100543	ORPHA:513436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0000011	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0000605	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0000666	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0001332	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0002079	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0002478	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0002518	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0003390	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0007256	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0001761	ORPHA:513436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0000317	ORPHA:513436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:513436	Autosomal recessive spastic paraplegia type 78		HP:0000726	ORPHA:513436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000003	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000075	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000076	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000125	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000126	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000212	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000316	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000478	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000480	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000482	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000483	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000486	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000505	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000508	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000518	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000539	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000545	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000568	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000612	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000615	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000648	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000678	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000684	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000692	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000767	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000768	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000932	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001089	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001159	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001166	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001181	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001347	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001371	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001492	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001636	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001641	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001642	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001647	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001650	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001680	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001746	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001763	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001822	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001847	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001848	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002007	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002019	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002021	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002540	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002572	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002650	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002719	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002750	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002857	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0003763	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0004313	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0004414	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0006482	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0007048	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0007328	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0009487	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0009918	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0010055	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0010511	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0011451	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0012385	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0012430	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0030791	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0040331	ORPHA:261552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000034	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000041	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000048	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000054	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000175	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000193	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000286	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000407	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001153	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001320	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001321	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001629	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001643	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002015	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002126	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002335	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002465	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002553	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002777	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0004961	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0005580	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0007099	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0007165	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001249	ORPHA:261552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001344	ORPHA:261552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001999	ORPHA:261552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002474	ORPHA:261552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0040082	ORPHA:261552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000020	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000028	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000047	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000119	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000179	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000194	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000303	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000307	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000322	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000358	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000403	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000431	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000437	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000444	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000490	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000506	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000707	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0000733	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001250	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001257	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001273	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001274	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001508	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0001627	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002079	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002136	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002251	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002353	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002360	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0002607	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0004322	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0005484	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0006956	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0007010	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0007270	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0007359	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0008947	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0009765	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0009909	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0011229	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0025100	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0030303	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0031936	ORPHA:261552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0011120	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0011317	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0011886	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0012081	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0030264	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0410005	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation		HP:0410031	ORPHA:261552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0004910	ORPHA:47159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0004918	ORPHA:47159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0001508	ORPHA:47159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0001510	ORPHA:47159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0002013	ORPHA:47159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0002900	ORPHA:47159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0003646	ORPHA:47159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000478	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000501	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000518	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000585	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000787	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000924	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0001249	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0001530	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0001944	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0001959	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0002014	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0002024	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0002150	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0003076	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0003109	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0003126	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0003149	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0003355	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0004349	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0006285	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0011106	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0012573	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0012605	ORPHA:47159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000121	ORPHA:47159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0000589	ORPHA:47159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0001682	ORPHA:47159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:47159	Proximal renal tubular acidosis		HP:0004322	ORPHA:47159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000023	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000154	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000248	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000252	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000272	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000280	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000286	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000307	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000325	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000343	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000348	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000431	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000448	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000486	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0000574	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001156	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001256	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001511	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001537	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001631	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001633	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001800	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001802	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001804	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001817	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0001857	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0002007	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0002086	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0002230	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0002750	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0004209	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0004322	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0004422	ORPHA:1292	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0008398	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0009773	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0009890	ORPHA:1292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0100797	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1292	Brachymorphism-onychodysplasia-dysphalangism syndrome		HP:0100798	ORPHA:1292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0001268	ORPHA:329308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002527	ORPHA:329308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007020	ORPHA:329308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007240	ORPHA:329308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0000605	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0000648	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0000666	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0001123	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0001260	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0001272	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002069	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002079	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002425	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002427	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002478	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002493	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002505	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0006827	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0006855	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007153	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007199	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007325	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007924	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0030584	ORPHA:329308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0000486	ORPHA:329308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007359	ORPHA:329308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0000716	ORPHA:329308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0000739	ORPHA:329308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0002015	ORPHA:329308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0007302	ORPHA:329308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329308	Fatty acid hydroxylase-associated neurodegeneration		HP:0009830	ORPHA:329308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000514	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000605	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000726	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001300	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002063	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002395	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0003487	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0007256	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0007350	ORPHA:306674	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000020	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000183	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000338	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000736	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001167	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001254	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001289	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001336	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002120	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001288	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002367	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002425	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0008969	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0010553	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0011446	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0012378	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0100660	ORPHA:306674	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000511	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000639	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000643	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000658	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0000741	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001260	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001268	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001276	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001288	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001760	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0001945	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002015	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002067	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002493	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0002607	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0003324	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0007083	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0025403	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306674	Kufor-Rakeb syndrome		HP:0031008	ORPHA:306674	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000951	ORPHA:35173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0010655	ORPHA:35173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000324	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000518	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000929	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0001019	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0002007	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0004322	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0004468	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0005280	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0006619	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0008064	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0025474	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0040189	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0100559	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0100560	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0100569	ORPHA:35173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000218	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000316	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000369	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000482	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000494	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000568	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000653	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0001197	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0001371	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0001597	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0001762	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0001998	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0002088	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0002208	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0002232	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0002751	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0002827	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0002999	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0004552	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0005756	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0008434	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0008443	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0008850	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0010720	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0045075	ORPHA:35173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000126	ORPHA:35173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000377	ORPHA:35173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0000407	ORPHA:35173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35173	X-linked dominant chondrodysplasia punctata		HP:0100702	ORPHA:35173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000054	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000164	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000176	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000193	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000248	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000252	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000303	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000307	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000309	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000316	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000327	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000348	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000455	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000470	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000486	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000506	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000520	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000607	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000664	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000670	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000767	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000808	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0002342	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0002553	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0002679	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0002684	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0002714	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0005280	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0008516	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0009748	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0009907	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0010299	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0010724	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0010749	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0011072	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0012368	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0100334	ORPHA:1299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000233	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000322	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000410	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000494	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0001363	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0003319	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0003423	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0006480	ORPHA:1299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000071	ORPHA:1299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000625	ORPHA:1299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0001250	ORPHA:1299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0000042	ORPHA:1299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0001537	ORPHA:1299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0001545	ORPHA:1299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0002561	ORPHA:1299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0002836	ORPHA:1299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0009814	ORPHA:1299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1299	Branchioskeletogenital syndrome		HP:0009818	ORPHA:1299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000003	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000104	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000126	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000202	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000218	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000232	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000268	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000358	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000377	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000405	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000431	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000455	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000482	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000486	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000508	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000518	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000579	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000582	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000589	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000612	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000691	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0000987	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0001028	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0001177	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0001511	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0001611	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0002002	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0002167	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0002216	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0004322	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0004464	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0004467	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0008606	ORPHA:1297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0009804	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0100268	ORPHA:1297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0100335	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1297	Branchio-oculo-facial syndrome		HP:0100798	ORPHA:1297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0001513	ORPHA:179494	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0003292	ORPHA:179494	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0000771	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0000786	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0000815	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0000842	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0002591	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0032218	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0005419	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0008187	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0008214	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0008724	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0008734	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0040171	ORPHA:179494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0000712	ORPHA:179494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0000831	ORPHA:179494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0002155	ORPHA:179494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0002788	ORPHA:179494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0004926	ORPHA:179494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0005616	ORPHA:179494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:179494	Obesity due to leptin receptor gene deficiency		HP:0008245	ORPHA:179494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0000023	ORPHA:1296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0000047	ORPHA:1296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0000154	ORPHA:1296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0000272	ORPHA:1296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0000384	ORPHA:1296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0000952	ORPHA:1296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0001249	ORPHA:1296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0001252	ORPHA:1296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0001396	ORPHA:1296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0001511	ORPHA:1296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0001531	ORPHA:1296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0001629	ORPHA:1296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0004313	ORPHA:1296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0005248	ORPHA:1296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0007360	ORPHA:1296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1296	Lambert syndrome		HP:0009794	ORPHA:1296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0000971	ORPHA:247257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0001945	ORPHA:247257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0011159	ORPHA:247257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0012378	ORPHA:247257	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0001289	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0002013	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0002094	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0002098	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0002546	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0002615	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0011029	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247257	Inhalational anthrax		HP:0100806	ORPHA:247257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000219	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000316	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000337	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000506	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0001053	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0001156	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0003196	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0005288	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0005916	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0009882	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0010624	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0010669	ORPHA:1295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000044	ORPHA:1295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000048	ORPHA:1295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000458	ORPHA:1295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0000664	ORPHA:1295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0001387	ORPHA:1295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0002857	ORPHA:1295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1295	Brachytelephalangy-dysmorphism-Kallmann syndrome		HP:0008736	ORPHA:1295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0001284	ORPHA:98771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0001324	ORPHA:98771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0002066	ORPHA:98771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0003474	ORPHA:98771	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0000365	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0001260	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0001310	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0001761	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0002395	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0002600	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0007141	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0010546	ORPHA:98771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0000639	ORPHA:98771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0001272	ORPHA:98771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0002346	ORPHA:98771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0003202	ORPHA:98771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0003477	ORPHA:98771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98771	Spinocerebellar ataxia type 18		HP:0030187	ORPHA:98771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0001251	ORPHA:98772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0001288	ORPHA:98772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0000020	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0001265	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0001272	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0001347	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0002070	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0002078	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0002172	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0006938	ORPHA:98772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0000602	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0000639	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0000651	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0001260	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0001350	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0002136	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0002311	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0002396	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98772	Spinocerebellar ataxia type 19/22		HP:0007772	ORPHA:98772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0002066	ORPHA:98773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0002071	ORPHA:98773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0002073	ORPHA:98773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0007944	ORPHA:98773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0000639	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0000708	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0001249	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0001260	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0001337	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0002063	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0002304	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0006855	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0010526	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0100543	ORPHA:98773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98773	Spinocerebellar ataxia type 21		HP:0000651	ORPHA:98773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86788	X-linked severe congenital neutropenia		HP:0001875	ORPHA:86788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86788	X-linked severe congenital neutropenia		HP:0002718	ORPHA:86788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86788	X-linked severe congenital neutropenia		HP:0012312	ORPHA:86788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0011970	ORPHA:85458	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0001250	ORPHA:85458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0001342	ORPHA:85458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0002120	ORPHA:85458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0002138	ORPHA:85458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0002315	ORPHA:85458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0002344	ORPHA:85458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0012520	ORPHA:85458	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0000726	ORPHA:85458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0002922	ORPHA:85458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0012229	ORPHA:85458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0025714	ORPHA:85458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85458	Cerebral Amyloid Angiopathy		HP:0030890	ORPHA:85458	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0010904	ORPHA:51208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0012335	ORPHA:51208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0012379	ORPHA:51208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0032164	ORPHA:51208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0500170	ORPHA:51208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0000750	ORPHA:51208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0001889	ORPHA:51208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0001903	ORPHA:51208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0010864	ORPHA:51208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0011342	ORPHA:51208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0012758	ORPHA:51208	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0000717	ORPHA:51208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51208	Formiminoglutamic aciduria		HP:0001631	ORPHA:51208	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0008245	ORPHA:226307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0031098	ORPHA:226307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0031219	ORPHA:226307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000158	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000270	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000282	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000871	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001254	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001265	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001510	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001537	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001662	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0002019	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0002045	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0004491	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0005930	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0005990	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0006579	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0008202	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0008828	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0008872	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0010627	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0012378	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0012758	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0031507	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0040075	ORPHA:226307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000044	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000407	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000470	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000609	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000824	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0000839	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001161	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001252	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001274	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001317	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001943	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0001999	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0002920	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0004637	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0005280	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0009381	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0011220	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0011755	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0011800	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0025502	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0030341	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0030344	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function		HP:0031218	ORPHA:226307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function	NOT	HP:0011437	ORPHA:226307	TAS					H	ORPHA:orphadata[2025-10-22]
ORPHA:226307	Hypothyroidism due to deficient transcription factors involved in pituitary development or function	NOT	HP:0025483	ORPHA:226307	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0000238	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0000369	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0000567	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0001249	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0001250	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0001263	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0001320	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002119	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002363	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002538	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002876	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0005949	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0008947	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0011968	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0040288	ORPHA:163961	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0000278	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0000316	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0000347	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0000358	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0001284	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0001305	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002007	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002015	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002033	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002245	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0002335	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0003196	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0005815	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0007738	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0007965	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163961	X-linked cerebral-cerebellar-coloboma syndrome		HP:0009928	ORPHA:163961	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001649	ORPHA:137675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0004755	ORPHA:137675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0004756	ORPHA:137675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000961	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000980	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001508	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001635	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001640	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001678	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001716	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001945	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0002013	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0002240	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0002329	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0002401	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0002789	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0003546	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0011712	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0011716	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0012735	ORPHA:137675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000107	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000147	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000175	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000238	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000485	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000568	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0000648	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001250	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001254	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001274	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001629	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001907	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0001943	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0002301	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0002438	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0003128	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0004749	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0005110	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0005165	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0005950	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0007185	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0007707	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0007957	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137675	Histiocytoid cardiomyopathy		HP:0100598	ORPHA:137675	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000154	ORPHA:163966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000238	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000322	ORPHA:163966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000347	ORPHA:163966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000369	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000457	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000568	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000883	ORPHA:163966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000926	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0000962	ORPHA:163966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0001256	ORPHA:163966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0001321	ORPHA:163966	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0001511	ORPHA:163966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0001522	ORPHA:163966	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0001773	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0002007	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0002866	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0003196	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0004279	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0004322	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0005871	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0006028	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0008364	ORPHA:163966	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type		HP:0008905	ORPHA:163966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001251	ORPHA:247245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0008619	ORPHA:247245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0009591	ORPHA:247245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001272	ORPHA:247245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001273	ORPHA:247245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001892	ORPHA:247245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0007240	ORPHA:247245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0007340	ORPHA:247245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0011029	ORPHA:247245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0100543	ORPHA:247245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0000009	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0000458	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0000726	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001260	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001310	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001350	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001934	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002013	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002018	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002070	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002075	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002138	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002143	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002315	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002317	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002321	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002334	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002354	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002359	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002921	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0002922	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0003401	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0003418	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0003487	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0003698	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0006827	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0007256	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0007328	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0007366	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0009916	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0010633	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0010829	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0032398	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0100006	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0100026	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0100952	ORPHA:247245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0001250	ORPHA:247245	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0030321	ORPHA:247245	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247245	Superficial siderosis		HP:0045052	ORPHA:247245	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0000666	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0001260	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0002015	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0002073	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0002141	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0001288	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0008003	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0010544	ORPHA:98767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0001332	ORPHA:98767	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0007256	ORPHA:98767	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98767	Spinocerebellar ataxia type 11		HP:0009830	ORPHA:98767	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0000639	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001256	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001260	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001263	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001270	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001272	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001290	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001347	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0002066	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0002070	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001288	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0006886	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0009046	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0010794	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0030187	ORPHA:98768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0000012	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0000020	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0000365	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0000473	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0000543	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0000648	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001336	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0002015	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0002172	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0002312	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0006801	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0008003	ORPHA:98768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001250	ORPHA:98768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0001999	ORPHA:98768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0002067	ORPHA:98768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0004322	ORPHA:98768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98768	Spinocerebellar ataxia type 13		HP:0025331	ORPHA:98768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0001251	ORPHA:98769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0001272	ORPHA:98769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0001347	ORPHA:98769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0002066	ORPHA:98769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0002345	ORPHA:98769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0002346	ORPHA:98769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0007351	ORPHA:98769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98769	Spinocerebellar ataxia type 15/16		HP:0030188	ORPHA:98769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0002066	ORPHA:98763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0001290	ORPHA:98763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0002070	ORPHA:98763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0002073	ORPHA:98763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0005109	ORPHA:98763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0006855	ORPHA:98763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0000640	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0001152	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0001260	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0001336	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0001337	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0002063	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0002600	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0003474	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98763	Spinocerebellar ataxia type 14		HP:0100543	ORPHA:98763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0000640	ORPHA:98764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0001260	ORPHA:98764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0001337	ORPHA:98764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0000718	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0001288	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0001761	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0002066	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0002070	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0002078	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0002354	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0001288	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0003390	ORPHA:98764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0000486	ORPHA:98764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0000642	ORPHA:98764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0000716	ORPHA:98764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0001256	ORPHA:98764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0001272	ORPHA:98764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0002378	ORPHA:98764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0002304	ORPHA:98764	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98764	Spinocerebellar ataxia type 27A		HP:0010526	ORPHA:98764	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0002495	ORPHA:98765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0003438	ORPHA:98765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0010830	ORPHA:98765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0010831	ORPHA:98765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0001251	ORPHA:98765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0001260	ORPHA:98765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0001288	ORPHA:98765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0002333	ORPHA:98765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0001284	ORPHA:98765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0003390	ORPHA:98765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0007002	ORPHA:98765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98765	Spinocerebellar ataxia type 4		HP:0009830	ORPHA:98765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98766	Spinocerebellar ataxia type 5		HP:0001272	ORPHA:98766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98766	Spinocerebellar ataxia type 5		HP:0001288	ORPHA:98766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98766	Spinocerebellar ataxia type 5		HP:0001350	ORPHA:98766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98766	Spinocerebellar ataxia type 5		HP:0002311	ORPHA:98766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0000639	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0000802	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0001251	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0001257	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0001272	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0001332	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0001347	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002063	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002066	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002067	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002070	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002172	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002317	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002464	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0006855	ORPHA:98760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0000020	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0000273	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0000716	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002015	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002495	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0002835	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0007772	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98760	Spinocerebellar ataxia type 8		HP:0012110	ORPHA:98760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001249	ORPHA:261537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001344	ORPHA:261537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001999	ORPHA:261537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002474	ORPHA:261537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0040082	ORPHA:261537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000020	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000028	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000047	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000119	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000179	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000194	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000303	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000307	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000322	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000358	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000403	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000431	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000437	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000444	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000490	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000506	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000733	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001250	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001257	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001273	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001274	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001508	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001627	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002079	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002136	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002251	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002353	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002360	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002607	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0004322	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0005484	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0006956	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0007010	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0007270	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0007359	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0008947	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0009765	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0009909	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0011229	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0025100	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0031936	ORPHA:261537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000003	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000075	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000076	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000125	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000126	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000212	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000316	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000480	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000483	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000486	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000508	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000518	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000545	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000568	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000612	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000678	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000684	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000692	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000767	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000768	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000932	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001159	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001166	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001181	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001371	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001492	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001636	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001641	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001642	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001647	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001650	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001680	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001746	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001763	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001822	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001847	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001848	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002019	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002021	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002540	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002572	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002650	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002719	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002750	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002857	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0003763	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0004313	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0004414	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0006482	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0007048	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0007328	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0009487	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0010055	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0010511	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0011451	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0012385	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0012430	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0040331	ORPHA:261537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000034	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000041	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000048	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000054	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000175	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000193	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0000407	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001153	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001320	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0001321	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002015	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002126	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002335	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002465	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0002777	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0004961	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0007099	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0007165	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0011317	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0012081	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0030264	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0410005	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22		HP:0410031	ORPHA:261537	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000026	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000054	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000062	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000286	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000303	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000316	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000347	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000358	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000431	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000708	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000729	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000744	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000750	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0001263	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000771	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000774	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0003241	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0000837	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0002750	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0001249	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0001776	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0001999	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0002119	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0002500	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0002788	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0003782	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0008193	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0008734	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0010506	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0011220	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0011343	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0040019	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0040171	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261534	49,XXXYY syndrome		HP:0045058	ORPHA:261534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0001260	ORPHA:98761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002066	ORPHA:98761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002073	ORPHA:98761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0000639	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0000640	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0001272	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0001310	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002075	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002080	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002141	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002168	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002197	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002317	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0007772	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0011198	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0030186	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0100660	ORPHA:98761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0000012	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0000716	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0000718	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0000741	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0001265	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0001290	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0001347	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002061	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002133	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002360	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0002384	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0003487	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98761	Spinocerebellar ataxia type 10		HP:0011153	ORPHA:98761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0001251	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0001272	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0001300	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0001317	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0001347	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002059	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002345	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002406	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0030188	ORPHA:98762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0000708	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0000726	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0001288	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002067	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002080	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002174	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002317	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0002375	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0007010	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0007141	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0007256	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98762	Spinocerebellar ataxia type 12		HP:0100543	ORPHA:98762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0003447	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0007078	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0012062	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0012185	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0012531	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0012534	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0000158	ORPHA:85446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0002015	ORPHA:85446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0002239	ORPHA:85446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0002242	ORPHA:85446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0003040	ORPHA:85446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0005106	ORPHA:85446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0005108	ORPHA:85446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0001635	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0002273	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0002445	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0003043	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0004389	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0011675	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0030843	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0100261	ORPHA:85446	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0001369	ORPHA:85446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0030833	ORPHA:85446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0030834	ORPHA:85446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0000762	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0001227	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85446	Wild type ABeta2M amyloidosis		HP:0003401	ORPHA:85446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001249	ORPHA:1272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001263	ORPHA:1272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0008897	ORPHA:1272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0012368	ORPHA:1272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000028	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000160	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000175	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000219	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000238	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000239	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000248	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000316	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000343	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000348	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000358	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000369	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000407	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000494	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000505	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000518	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000519	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000582	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000586	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000677	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001182	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001250	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001357	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001376	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001488	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001838	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002119	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002120	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002209	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002353	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0003196	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0004209	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0004322	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0005280	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0005487	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0007099	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0008551	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0008947	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0011333	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0012385	ORPHA:1272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000023	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000093	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000270	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000402	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000485	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000501	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000527	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000765	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0000776	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001363	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001643	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001698	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0001701	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002079	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002373	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002650	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002680	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0002974	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0003187	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0005815	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0012770	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1272	Aymé-Gripp syndrome		HP:0030680	ORPHA:1272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0000112	ORPHA:85447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0001271	ORPHA:85447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0000802	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0001638	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0001640	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0001678	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0001824	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0002014	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0002019	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0011675	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0012185	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0012211	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0012332	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85447	ATTRV30M amyloidosis		HP:0100832	ORPHA:85447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0000252	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0000340	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0000347	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0000448	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0001387	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0001522	ORPHA:1270	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0004322	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0008850	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0008872	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0011344	ORPHA:1270	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0000028	ORPHA:1270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0001838	ORPHA:1270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0004209	ORPHA:1270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0008846	ORPHA:1270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0100490	ORPHA:1270	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0000202	ORPHA:1270	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0001250	ORPHA:1270	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0002101	ORPHA:1270	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0002119	ORPHA:1270	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1270	Bowen-Conradi syndrome		HP:0030680	ORPHA:1270	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289601	Hereditary arterial and articular multiple calcification syndrome		HP:0003207	ORPHA:289601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289601	Hereditary arterial and articular multiple calcification syndrome		HP:0011025	ORPHA:289601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289601	Hereditary arterial and articular multiple calcification syndrome		HP:0025015	ORPHA:289601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289601	Hereditary arterial and articular multiple calcification syndrome		HP:0025324	ORPHA:289601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289601	Hereditary arterial and articular multiple calcification syndrome		HP:0012101	ORPHA:289601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289601	Hereditary arterial and articular multiple calcification syndrome		HP:0001717	ORPHA:289601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289601	Hereditary arterial and articular multiple calcification syndrome		HP:0005116	ORPHA:289601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000478	ORPHA:85448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000958	ORPHA:85448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001005	ORPHA:85448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001097	ORPHA:85448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001149	ORPHA:85448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001488	ORPHA:85448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000217	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000365	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000505	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000518	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000707	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000969	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000973	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000978	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001251	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001271	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0002015	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0002411	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0007067	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0007663	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0010628	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0011356	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0011675	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0012185	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0012804	ORPHA:85448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000093	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000501	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000597	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000763	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000989	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001260	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0001638	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0004926	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0007488	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0008070	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0010535	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0010749	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0012473	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0025408	ORPHA:85448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0000716	ORPHA:85448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0002483	ORPHA:85448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0002549	ORPHA:85448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0003774	ORPHA:85448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0008404	ORPHA:85448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85448	AGel amyloidosis		HP:0011947	ORPHA:85448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0012378	ORPHA:85443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0000077	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0000093	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0000100	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0001627	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0001639	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0001824	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0002024	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0003115	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0006530	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0007141	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0010702	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0012280	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0012592	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0025077	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0025552	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0031185	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0031326	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0032613	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0100639	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0410173	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0410174	ORPHA:85443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0000083	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0000217	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0000978	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0001713	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0001903	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0002094	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0002240	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0002870	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0003073	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0003155	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0003270	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0005120	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0005307	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0008321	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0008652	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0009830	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0010286	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0011675	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0012185	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0012332	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0012398	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0025389	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0030164	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0031246	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0031595	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0032550	ORPHA:85443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0000158	ORPHA:85443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0001609	ORPHA:85443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0002015	ORPHA:85443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0002239	ORPHA:85443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0002578	ORPHA:85443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis		HP:0011024	ORPHA:85443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85443	AL amyloidosis	NOT	HP:0012664	ORPHA:85443	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000093	ORPHA:85445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000112	ORPHA:85445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0001917	ORPHA:85445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0002615	ORPHA:85445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0011034	ORPHA:85445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000100	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000105	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0001396	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0002013	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0002018	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0002024	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0002027	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0002028	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0002240	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0004395	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0004936	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0011830	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0012622	ORPHA:85445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000083	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000853	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0001278	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0001744	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0001919	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0005162	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0009830	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0012185	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0025077	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0030164	ORPHA:85445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000158	ORPHA:85445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000821	ORPHA:85445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0000846	ORPHA:85445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85445	AA amyloidosis		HP:0030843	ORPHA:85445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000093	ORPHA:85450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000112	ORPHA:85450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0032613	ORPHA:85450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000083	ORPHA:85450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000822	ORPHA:85450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0001970	ORPHA:85450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0003259	ORPHA:85450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0011024	ORPHA:85450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0012213	ORPHA:85450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0012591	ORPHA:85450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000017	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000092	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000100	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000967	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000979	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0001410	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0001433	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0001635	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0001824	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0001903	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002013	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002014	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002018	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002020	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002027	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002239	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002240	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002716	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0002733	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0003198	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0003233	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0003565	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0005214	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0005576	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0009830	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0031368	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0031799	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0410281	ORPHA:85450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000035	ORPHA:85450	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000135	ORPHA:85450	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0000798	ORPHA:85450	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0003251	ORPHA:85450	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85450	Hereditary amyloidosis with primary renal involvement		HP:0008720	ORPHA:85450	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0000174	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0000347	ORPHA:1278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0000431	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0000574	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0000664	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0001156	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0001177	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0001231	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0002007	ORPHA:1278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0006433	ORPHA:1278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0010049	ORPHA:1278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0010743	ORPHA:1278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1278	Brachydactyly-preaxial hallux varus syndrome		HP:0011304	ORPHA:1278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000026	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000028	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000047	ORPHA:163971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000252	ORPHA:163971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000336	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000400	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000426	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000490	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000709	ORPHA:163971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000815	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0000837	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0002750	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0004209	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0001256	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0001508	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0004322	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0001792	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0001999	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0008187	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0008734	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0004440	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0011999	ORPHA:163971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0040171	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0100962	ORPHA:163971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163971	X-linked intellectual disability, Cilliers type		HP:0200055	ORPHA:163971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0000853	ORPHA:226316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0002925	ORPHA:226316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0008263	ORPHA:226316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0025484	ORPHA:226316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0031507	ORPHA:226316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0000158	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0001070	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0001254	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0001537	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0001615	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0002019	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0006579	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0011437	ORPHA:226316	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0011968	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0031169	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0031221	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0100786	ORPHA:226316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0000969	ORPHA:226316	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0001252	ORPHA:226316	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0002045	ORPHA:226316	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:226316	Genetic transient congenital hypothyroidism		HP:0005990	ORPHA:226316	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001692	ORPHA:85451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0003115	ORPHA:85451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0030843	ORPHA:85451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0031185	ORPHA:85451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0410174	ORPHA:85451	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001639	ORPHA:85451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001640	ORPHA:85451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001723	ORPHA:85451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0005150	ORPHA:85451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0011675	ORPHA:85451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0012664	ORPHA:85451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001297	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001635	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001681	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001712	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001903	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001907	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0003416	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0012185	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0012332	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0025028	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0100550	ORPHA:85451	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001271	ORPHA:85451	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0001650	ORPHA:85451	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85451	ATTRV122I amyloidosis		HP:0009830	ORPHA:85451	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0000174	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0000347	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0000444	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0001156	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0001633	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0003027	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0003043	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0004299	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0009804	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0100543	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1277	Brachydactyly-mesomelia-intellectual disability-heart defects syndrome		HP:0100818	ORPHA:1277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1276	Brachydactyly-arterial hypertension syndrome		HP:0000822	ORPHA:1276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1276	Brachydactyly-arterial hypertension syndrome		HP:0001156	ORPHA:1276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1276	Brachydactyly-arterial hypertension syndrome		HP:0004322	ORPHA:1276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1276	Brachydactyly-arterial hypertension syndrome		HP:0009803	ORPHA:1276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1276	Brachydactyly-arterial hypertension syndrome		HP:0010049	ORPHA:1276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0025104	ORPHA:137667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0011276	ORPHA:137667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0000421	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001004	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001009	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001722	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001892	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0002408	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0002637	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0004947	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0009127	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0012733	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0030713	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0100026	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0100763	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0100784	ORPHA:137667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0000011	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0000238	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0000996	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001028	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001250	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001627	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001635	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0001790	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0002076	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0002315	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0004302	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0010310	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137667	Capillary malformation-arteriovenous malformation		HP:0020073	ORPHA:137667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0000256	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0001156	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0001231	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0001387	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0003042	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0031095	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0004209	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0005048	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0006501	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0009832	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1275	Brachydactyly-elbow wrist dysplasia syndrome		HP:0040071	ORPHA:1275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0000851	ORPHA:226313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0000853	ORPHA:226313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0002925	ORPHA:226313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0003270	ORPHA:226313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0031507	ORPHA:226313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0000158	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0001070	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0001265	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0001319	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0001520	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0001537	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0001538	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0002019	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0002045	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0002663	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0005280	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0005930	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0006579	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0008820	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0008872	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0100786	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0500011	ORPHA:226313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0000958	ORPHA:226313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0001662	ORPHA:226313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0002098	ORPHA:226313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:226313	Congenital hypothyroidism due to maternal intake of antithyroid drugs		HP:0004491	ORPHA:226313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000496	ORPHA:247234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0001251	ORPHA:247234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002066	ORPHA:247234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000572	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000608	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000640	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002354	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0007670	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0007772	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0008278	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0012332	ORPHA:247234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000338	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000763	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0001257	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0001260	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0001291	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0001300	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0001347	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002015	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002063	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002075	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002304	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002322	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002362	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0003487	ORPHA:247234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000020	ORPHA:247234	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0000726	ORPHA:247234	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247234	Sporadic adult-onset ataxia of unknown etiology		HP:0002080	ORPHA:247234	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0000572	ORPHA:59181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0007754	ORPHA:59181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0030500	ORPHA:59181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0031528	ORPHA:59181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0000610	ORPHA:59181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0000662	ORPHA:59181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0001129	ORPHA:59181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0011506	ORPHA:59181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0030491	ORPHA:59181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0030602	ORPHA:59181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0030625	ORPHA:59181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0000533	ORPHA:59181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0000580	ORPHA:59181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0000618	ORPHA:59181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0001105	ORPHA:59181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0001141	ORPHA:59181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59181	Sorsby pseudoinflammatory fundus dystrophy		HP:0007722	ORPHA:59181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0000026	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0000028	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0000252	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0000278	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0012760	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0000815	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0000837	ORPHA:163976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0002750	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0004209	ORPHA:163976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0001256	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0001508	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0004322	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0001511	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0005978	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0007018	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0008187	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0008551	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0008734	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0004440	ORPHA:163976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0012646	ORPHA:163976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163976	X-linked intellectual disability, Van Esch type		HP:0040171	ORPHA:163976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0002073	ORPHA:98756	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0045007	ORPHA:98756	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0000514	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0000623	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0000639	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0000726	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0001260	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0001265	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0001290	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0001332	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0002066	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0002072	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0002174	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0002380	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0003133	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0003394	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0006955	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0008311	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0012082	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0025461	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0030186	ORPHA:98756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0000597	ORPHA:98756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0001300	ORPHA:98756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0002120	ORPHA:98756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0002536	ORPHA:98756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0006801	ORPHA:98756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98756	Spinocerebellar ataxia type 2		HP:0012762	ORPHA:98756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0000520	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0000590	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0000639	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0000651	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0000750	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0001260	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0001332	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0001347	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0002071	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0002073	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0002312	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0003202	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0007256	ORPHA:98757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0001605	ORPHA:98757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0001751	ORPHA:98757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98757	Spinocerebellar ataxia type 3		HP:0004370	ORPHA:98757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0000639	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0002066	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0002073	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0002080	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0002172	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0002311	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0002317	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0007979	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0030511	ORPHA:98758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0000504	ORPHA:98758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0000651	ORPHA:98758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0001347	ORPHA:98758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0002015	ORPHA:98758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0003487	ORPHA:98758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0010544	ORPHA:98758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0030842	ORPHA:98758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0000643	ORPHA:98758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0001260	ORPHA:98758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98758	Spinocerebellar ataxia type 6		HP:0001332	ORPHA:98758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0001251	ORPHA:98759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0001288	ORPHA:98759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0000473	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0000643	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0000708	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0001257	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0001268	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0001272	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0001300	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0001332	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0002063	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0002072	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0002529	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0004305	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0007058	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0007256	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0007366	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0012082	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98759	Spinocerebellar ataxia type 17		HP:0002356	ORPHA:98759	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000026	ORPHA:261529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000027	ORPHA:261529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000028	ORPHA:261529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000033	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000047	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000048	ORPHA:261529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000051	ORPHA:261529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000061	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000133	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000150	ORPHA:261529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000771	ORPHA:261529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0004322	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0001513	ORPHA:261529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0003251	ORPHA:261529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0008222	ORPHA:261529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0008669	ORPHA:261529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0000062	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0010460	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0010461	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0010464	ORPHA:261529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0012741	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261529	Ring chromosome Y syndrome		HP:0100779	ORPHA:261529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000064	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000486	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000708	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000709	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000717	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000729	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000786	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000789	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000823	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000824	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001252	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001256	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001328	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001508	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001773	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002205	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002591	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002650	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0003241	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0004322	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0006889	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0008734	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0010627	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0011734	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0012104	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0012105	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0012650	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0025160	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0030339	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0031169	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0200055	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000819	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000938	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000939	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001250	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001263	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001385	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001518	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001558	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002360	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002578	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002714	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002870	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002871	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0007874	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0010741	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0010829	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0011787	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0012166	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0012411	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0012412	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0031100	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0031507	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0100716	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0100739	ORPHA:98754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000826	ORPHA:98754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001010	ORPHA:98754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002342	ORPHA:98754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0005599	ORPHA:98754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0007730	ORPHA:98754	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000028	ORPHA:98754	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0001513	ORPHA:98754	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0002119	ORPHA:98754	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0008872	ORPHA:98754	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000044	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000046	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98754	Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15		HP:0000060	ORPHA:98754	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002073	ORPHA:98755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0009830	ORPHA:98755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0000496	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0000514	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001260	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001272	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001288	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001332	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001350	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002015	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002067	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002072	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002354	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002483	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0007001	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0007366	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0007377	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0007928	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0025331	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0025401	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0030216	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0040129	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0100543	ORPHA:98755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0000597	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0000639	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0000648	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001265	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001290	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0001310	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002075	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002141	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002174	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002363	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002380	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0002878	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0003202	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0006801	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0007338	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0010831	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98755	Spinocerebellar ataxia type 1		HP:0410011	ORPHA:98755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0000054	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0000358	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0000470	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0006610	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0000789	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0000914	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0010049	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0001249	ORPHA:261524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0001252	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0001256	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0001263	ORPHA:261524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0004322	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0002162	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0002916	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0002967	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0100853	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0008734	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261524	Paternal uniparental disomy of chromosome X syndrome		HP:0011343	ORPHA:261524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0001250	ORPHA:2590	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0001336	ORPHA:2590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002366	ORPHA:2590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0004302	ORPHA:2590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0007340	ORPHA:2590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0012379	ORPHA:2590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0000708	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0001337	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002100	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002123	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002312	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0001288	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002359	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002747	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0010819	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0011147	ORPHA:2590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0000407	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0001268	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0001757	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002515	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002540	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002650	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002878	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0025097	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0025190	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0032667	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0045084	ORPHA:2590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0001249	ORPHA:2590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome		HP:0002015	ORPHA:2590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome	NOT	HP:0001371	ORPHA:2590	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome	NOT	HP:0001433	ORPHA:2590	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome	NOT	HP:0001609	ORPHA:2590	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2590	Spinal muscular atrophy-progressive myoclonic epilepsy syndrome	NOT	HP:0200036	ORPHA:2590	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000077	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000169	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000271	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000478	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000765	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000929	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000934	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0000944	ORPHA:2591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0001376	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0001482	ORPHA:2591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0001595	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0002242	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0002575	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0002797	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0002894	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0003011	ORPHA:2591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0003072	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0004374	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0005107	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0005214	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0007400	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0008069	ORPHA:2591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0010614	ORPHA:2591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0012062	ORPHA:2591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0100242	ORPHA:2591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0100526	ORPHA:2591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0100835	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2591	Infantile myofibromatosis		HP:0200042	ORPHA:2591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0000252	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0000268	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0000347	ORPHA:1261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0000505	ORPHA:1261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0000824	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0001256	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0001257	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0002119	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0002353	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0002514	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1261	Bonnemann-Meinecke-Reich syndrome		HP:0004322	ORPHA:1261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0001369	ORPHA:85435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0002829	ORPHA:85435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0002923	ORPHA:85435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0005764	ORPHA:85435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0001376	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0001386	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0002813	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0003565	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0005187	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0005930	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0006252	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0011227	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0011117	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0040311	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0100769	ORPHA:85435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0000938	ORPHA:85435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0004349	ORPHA:85435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0010588	ORPHA:85435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85435	Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis		HP:0100555	ORPHA:85435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000609	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000648	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000729	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0001257	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0001344	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0001508	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0002063	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0002317	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0002650	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0003508	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0100660	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000253	ORPHA:163937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0001321	ORPHA:163937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0002342	ORPHA:163937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0011344	ORPHA:163937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0012110	ORPHA:163937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000252	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000278	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000316	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000337	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000343	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000347	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000400	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000407	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000431	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000455	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000486	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000505	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000545	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000639	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0001250	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0001288	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0001332	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0002120	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0002360	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0002553	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0003196	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0008872	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0008936	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0008947	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0011097	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0012171	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0032794	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0034353	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0200134	ORPHA:163937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163937	X-linked intellectual disability, Najm type		HP:0000543	ORPHA:163937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0011118	ORPHA:85436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0000989	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0001369	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0001803	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0002829	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0002960	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0003493	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0003765	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0005764	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0031090	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0031091	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0040313	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0100686	ORPHA:85436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0000554	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0000988	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0001376	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0002815	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0003019	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0003043	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0005197	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0007663	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0012122	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0025300	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0025526	ORPHA:85436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0001094	ORPHA:85436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0001101	ORPHA:85436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0001806	ORPHA:85436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0010754	ORPHA:85436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85436	Psoriasis-related juvenile idiopathic arthritis		HP:0012317	ORPHA:85436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0040313	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0100536	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0100712	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0001627	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0001760	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0001832	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0003019	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0003043	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0003319	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0001369	ORPHA:85438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0002829	ORPHA:85438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0100686	ORPHA:85438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0000925	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0001384	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0003028	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0003418	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0004690	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0005086	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0008364	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0008843	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0012317	ORPHA:85438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0003366	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0006217	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0007813	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0009811	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0011842	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0011911	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0012122	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0031090	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0100711	ORPHA:85438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0000794	ORPHA:85438	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0001634	ORPHA:85438	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0001659	ORPHA:85438	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85438	Enthesitis-related juvenile idiopathic arthritis		HP:0006698	ORPHA:85438	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0000016	ORPHA:1267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0000217	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0000651	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0001260	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0002014	ORPHA:1267	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0002015	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0002017	ORPHA:1267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0002019	ORPHA:1267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0002027	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0002093	ORPHA:1267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0006597	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0006824	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0010547	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0011499	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0011675	ORPHA:1267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0100021	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0009113	ORPHA:1267	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1267	Botulism		HP:0012378	ORPHA:1267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0001873	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0001882	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0002014	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0002027	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0006562	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0012378	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0033834	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:6001005	ORPHA:137698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0001399	ORPHA:137698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0006515	ORPHA:137698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0012486	ORPHA:137698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0033431	ORPHA:137698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0033993	ORPHA:137698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137698	Cytomegalovirus disease in patients with impaired cell mediated immunity deemed at risk		HP:0032118	ORPHA:137698	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0000164	ORPHA:1264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0001118	ORPHA:1264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0001156	ORPHA:1264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0007703	ORPHA:1264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0008070	ORPHA:1264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0030056	ORPHA:1264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0000677	ORPHA:1264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0001155	ORPHA:1264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0011069	ORPHA:1264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1264	Tricho-retino-dento-digital syndrome		HP:0010047	ORPHA:1264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0000774	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0000824	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0002983	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0002992	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0006492	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0008890	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0011849	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0100569	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0100856	ORPHA:1263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0000028	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0001539	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0001561	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0001789	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0002818	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0002823	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0031095	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0005916	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0006101	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0006703	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0010318	ORPHA:1263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1263	Boomerang dysplasia		HP:0040071	ORPHA:1263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0000164	ORPHA:1262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0000189	ORPHA:1262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0000534	ORPHA:1262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0000668	ORPHA:1262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0000975	ORPHA:1262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0001804	ORPHA:1262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0002216	ORPHA:1262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0007477	ORPHA:1262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0007598	ORPHA:1262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1262	Böök syndrome		HP:0200055	ORPHA:1262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001250	ORPHA:352582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0002123	ORPHA:352582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001260	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001272	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0006891	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0007359	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0011171	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0011197	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0025190	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0025373	ORPHA:352582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0000520	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0000643	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0000750	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001251	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001256	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001263	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001270	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0001288	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0002069	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0002312	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0002342	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0006889	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0025100	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0032388	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352582	Familial infantile myoclonic epilepsy		HP:0045084	ORPHA:352582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0003326	ORPHA:2593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0003394	ORPHA:2593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0003458	ORPHA:2593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0003473	ORPHA:2593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0030200	ORPHA:2593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0100301	ORPHA:2593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0003557	ORPHA:2593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0003687	ORPHA:2593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2593	Tubular aggregate myopathy		HP:0003554	ORPHA:2593	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003756	ORPHA:2596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0007126	ORPHA:2596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0100651	ORPHA:2596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0002395	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0002540	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003487	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003546	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003547	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003551	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0009046	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0009073	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0012391	ORPHA:2596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0001260	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0002073	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0002098	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0002342	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0002359	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003326	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003477	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0003749	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0008944	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0012036	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0012507	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0030051	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0030319	ORPHA:2596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0000407	ORPHA:2596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0000726	ORPHA:2596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0001319	ORPHA:2596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0001771	ORPHA:2596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0002495	ORPHA:2596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0031258	ORPHA:2596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2596	Myopathy and diabetes mellitus		HP:0100753	ORPHA:2596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0000407	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0001250	ORPHA:2597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0001942	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0003198	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0003202	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0003348	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0003457	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0003737	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2597	Mitochondrial myopathy-lactic acidosis-deafness syndrome		HP:0004320	ORPHA:2597	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0000218	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0000252	ORPHA:2598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0000343	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0000347	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0000501	ORPHA:2598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0000823	ORPHA:2598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0001249	ORPHA:2598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0001252	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0001903	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0001939	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0002650	ORPHA:2598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0002808	ORPHA:2598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0003128	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0003196	ORPHA:2598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0003198	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0003457	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0003737	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0009055	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2598	Mitochondrial myopathy and sideroblastic anemia		HP:0009743	ORPHA:2598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0000027	ORPHA:261519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0000062	ORPHA:261519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0000233	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0000252	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0000470	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0000914	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001010	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001249	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001250	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001274	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001263	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001371	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001399	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0004322	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001635	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0001838	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0002162	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0002650	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0002916	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0002967	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0003186	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0003248	ORPHA:261519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0003550	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0005280	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0008193	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261519	Maternal uniparental disomy of chromosome X syndrome		HP:0100490	ORPHA:261519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0000140	ORPHA:137686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0000868	ORPHA:137686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0000876	ORPHA:137686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0000789	ORPHA:137686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0000869	ORPHA:137686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0002574	ORPHA:137686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0005268	ORPHA:137686	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0100607	ORPHA:137686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0100608	ORPHA:137686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0031035	ORPHA:137686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137686	Asherman syndrome		HP:0100767	ORPHA:137686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000177	ORPHA:1253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000218	ORPHA:1253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000316	ORPHA:1253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000445	ORPHA:1253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000492	ORPHA:1253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000505	ORPHA:1253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000508	ORPHA:1253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000581	ORPHA:1253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000821	ORPHA:1253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0000853	ORPHA:1253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0004097	ORPHA:1253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1253	Ascher syndrome		HP:0012724	ORPHA:1253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000154	ORPHA:163956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000958	ORPHA:163956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002194	ORPHA:163956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002465	ORPHA:163956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0009765	ORPHA:163956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000054	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000076	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000233	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000256	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000316	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000475	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000582	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000664	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000718	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001250	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001629	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001761	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001773	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002162	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002230	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002500	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002714	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0003265	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0005280	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0006610	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0007103	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0010529	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0010864	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0012450	ORPHA:163956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000028	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000047	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000348	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000365	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000400	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000430	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000486	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000519	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0000722	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001562	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001636	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001643	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001655	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001718	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001719	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001776	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001845	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0001875	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002002	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002092	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002205	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0002342	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0004467	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0004969	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0005345	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0007509	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0008404	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0010721	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0011800	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0011913	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0012110	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0030311	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0100760	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0100838	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163956	X-linked intellectual disability, Nascimento type		HP:0410018	ORPHA:163956	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000023	ORPHA:1252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000028	ORPHA:1252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000175	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000286	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000298	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000343	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000365	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000430	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000431	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000445	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000499	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000506	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000581	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000632	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000648	ORPHA:1252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0001072	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0001249	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0001304	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0001347	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0001582	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0001608	ORPHA:1252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0002162	ORPHA:1252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0005338	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0001382	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0006101	ORPHA:1252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0000377	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0009804	ORPHA:1252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1252	Blepharonasofacial malformation syndrome		HP:0100335	ORPHA:1252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0001025	ORPHA:2582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0001072	ORPHA:2582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0001369	ORPHA:2582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0001376	ORPHA:2582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0001880	ORPHA:2582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0001888	ORPHA:2582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0002103	ORPHA:2582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0003011	ORPHA:2582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0005469	ORPHA:2582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2582	Myalgia-eosinophilia syndrome associated with tryptophan		HP:0007328	ORPHA:2582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0001015	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0001482	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0002841	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0003330	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0005406	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0010219	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0030053	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0031288	ORPHA:2583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0000939	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0001155	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0002754	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0002815	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0011844	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0025245	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0040072	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0100763	ORPHA:2583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0000152	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0000707	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0000765	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0002661	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0002756	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0002953	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0003312	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0003418	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0010550	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0012062	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0031500	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0031501	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2583	Mycetoma		HP:0100809	ORPHA:2583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0000958	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0000964	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0000988	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0000989	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0002665	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0004332	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0008069	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0010783	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0200035	ORPHA:2584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001029	ORPHA:2584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001053	ORPHA:2584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001596	ORPHA:2584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0002716	ORPHA:2584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0007400	ORPHA:2584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0012192	ORPHA:2584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0025475	ORPHA:2584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0000492	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0000962	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0000969	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001019	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001597	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001744	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0002240	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0005561	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0007488	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0200042	ORPHA:2584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001824	ORPHA:2584	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0001945	ORPHA:2584	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2584	Classic mycosis fungoides		HP:0030166	ORPHA:2584	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0000252	ORPHA:2585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0000639	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001251	ORPHA:2585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001272	ORPHA:2585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001288	ORPHA:2585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001347	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001744	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001874	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001876	ORPHA:2585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0001908	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0002167	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0002205	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0002317	ORPHA:2585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0004311	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0004313	ORPHA:2585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0004820	ORPHA:2585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0007360	ORPHA:2585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2585	Ataxia-pancytopenia syndrome		HP:0011869	ORPHA:2585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001249	ORPHA:352577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001263	ORPHA:352577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002167	ORPHA:352577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0008872	ORPHA:352577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0008947	ORPHA:352577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000252	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000486	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000729	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000924	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001344	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002187	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002705	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0010864	ORPHA:352577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000194	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000232	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000268	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000316	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000414	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000426	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000430	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000494	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000582	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000664	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0000678	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001166	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001250	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001276	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001320	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001519	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0001763	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002342	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002360	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002500	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002540	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002553	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0002650	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0003189	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0004673	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0009765	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0011220	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352577	Bainbridge-Ropers syndrome		HP:0100023	ORPHA:352577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000160	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000233	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000303	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000327	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000365	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000772	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000926	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001156	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001249	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001263	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001328	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001387	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001511	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0003172	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0003510	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0003712	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0004279	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0004493	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0008818	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0011800	ORPHA:2588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000028	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000159	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000508	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000581	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000822	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000944	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001072	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0001671	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0003457	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0005930	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0008499	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0012745	ORPHA:2588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000023	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000036	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000039	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000047	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000135	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000175	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000176	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000193	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000518	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000708	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0000826	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0003241	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0030690	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0100333	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2588	Myhre syndrome		HP:0100541	ORPHA:2588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0000269	ORPHA:1259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0000501	ORPHA:1259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0000508	ORPHA:1259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0000545	ORPHA:1259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0000612	ORPHA:1259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0001083	ORPHA:1259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0007703	ORPHA:1259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0011039	ORPHA:1259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0100540	ORPHA:1259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1259	Blepharoptosis-myopia-ectopia lentis syndrome		HP:0100798	ORPHA:1259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0001260	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0001336	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0002073	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0002080	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0002522	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0003445	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0003700	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0007141	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0007240	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2589	Myoclonus-cerebellar ataxia-deafness syndrome		HP:0008619	ORPHA:2589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0000252	ORPHA:2570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0000340	ORPHA:2570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0000347	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0000369	ORPHA:2570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0000470	ORPHA:2570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0000490	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0000581	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0001181	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0001360	ORPHA:2570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0001376	ORPHA:2570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0001511	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0001558	ORPHA:2570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0002103	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0002120	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0002324	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0002828	ORPHA:2570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0006703	ORPHA:2570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0007360	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0007370	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0007477	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0008678	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0010662	ORPHA:2570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0100490	ORPHA:2570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2570	Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome		HP:0100625	ORPHA:2570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2579	Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome		HP:0001251	ORPHA:2579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2579	Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome		HP:0003198	ORPHA:2579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2579	Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome		HP:0005978	ORPHA:2579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2579	Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome		HP:0007703	ORPHA:2579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139414	Congenital panfollicular nevus		HP:0010566	ORPHA:139414	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139414	Congenital panfollicular nevus		HP:0012500	ORPHA:139414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139414	Congenital panfollicular nevus		HP:0200036	ORPHA:139414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139414	Congenital panfollicular nevus		HP:0000962	ORPHA:139414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139414	Congenital panfollicular nevus	NOT	HP:0000989	ORPHA:139414	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:139414	Congenital panfollicular nevus	NOT	HP:0012531	ORPHA:139414	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0000822	ORPHA:139411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0001541	ORPHA:139411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0001649	ORPHA:139411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0001903	ORPHA:139411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002014	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002017	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002027	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002039	ORPHA:139411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002113	ORPHA:139411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002239	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002315	ORPHA:139411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002666	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002668	ORPHA:139411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002716	ORPHA:139411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0002717	ORPHA:139411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0008256	ORPHA:139411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0011675	ORPHA:139411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0012378	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0100243	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0100721	ORPHA:139411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139411	Carney triad		HP:0100723	ORPHA:139411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1243	Best vitelliform macular dystrophy		HP:0000505	ORPHA:1243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1243	Best vitelliform macular dystrophy		HP:0000551	ORPHA:1243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1243	Best vitelliform macular dystrophy		HP:0001123	ORPHA:1243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1243	Best vitelliform macular dystrophy		HP:0001139	ORPHA:1243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1243	Best vitelliform macular dystrophy		HP:0008028	ORPHA:1243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1243	Best vitelliform macular dystrophy		HP:0012508	ORPHA:1243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000486	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000508	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000542	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000577	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0001491	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0011347	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0012241	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0025721	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0030211	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0030534	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:6000709	ORPHA:45358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000512	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000539	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000616	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000646	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0001477	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0007831	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0012547	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0025309	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0030588	ORPHA:45358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000044	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000473	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000518	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000565	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0000609	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0009380	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0001249	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0001252	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0001357	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0002013	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0002126	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0002194	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0008527	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0009916	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0025186	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:45358	Congenital fibrosis of extraocular muscles		HP:0032466	ORPHA:45358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0001324	ORPHA:139417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002071	ORPHA:139417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002922	ORPHA:139417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0003474	ORPHA:139417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0012229	ORPHA:139417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0012332	ORPHA:139417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:5000013	ORPHA:139417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0000016	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0000020	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0000822	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0001257	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0001278	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0001287	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0001288	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0001347	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0001945	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002019	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002138	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002385	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002493	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002495	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002578	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002590	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002721	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002725	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002839	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0002960	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0003401	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0003418	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0003484	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0003487	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0004370	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0005341	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0007305	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0009053	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0010547	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0010550	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0010831	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0010835	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0011967	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0011972	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0012378	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0012534	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0025615	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0031179	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0031691	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0031700	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0031845	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0032271	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0032283	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0032492	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0100502	ORPHA:139417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139417	Acute transverse myelitis		HP:0200023	ORPHA:139417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0000176	ORPHA:1241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0000324	ORPHA:1241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0000486	ORPHA:1241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0000506	ORPHA:1241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0000582	ORPHA:1241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0000646	ORPHA:1241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0005325	ORPHA:1241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1241	Bencze syndrome		HP:0010807	ORPHA:1241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000044	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000141	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000789	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000824	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000938	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0001943	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0002615	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0002920	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0005625	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0012378	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0040086	ORPHA:95619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000823	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000863	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0000871	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0001510	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0002750	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0008245	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0008734	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0009888	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95619	Post-traumatic pituitary deficiency		HP:0010311	ORPHA:95619	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0000009	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0000639	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0000662	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0001276	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0001347	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0002205	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0004374	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0008348	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0012638	ORPHA:2571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0000518	ORPHA:2571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0002103	ORPHA:2571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2571	X-linked immunoneurologic disorder		HP:0003198	ORPHA:2571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0000519	ORPHA:2572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0000545	ORPHA:2572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0000648	ORPHA:2572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0001131	ORPHA:2572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0001251	ORPHA:2572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0001288	ORPHA:2572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0002497	ORPHA:2572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0002503	ORPHA:2572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0003457	ORPHA:2572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0004313	ORPHA:2572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0004374	ORPHA:2572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2572	Spastic ataxia-corneal dystrophy syndrome		HP:0007360	ORPHA:2572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2573	Moyamoya disease		HP:0001009	ORPHA:2573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2573	Moyamoya disease		HP:0001249	ORPHA:2573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2573	Moyamoya disease		HP:0001250	ORPHA:2573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2573	Moyamoya disease		HP:0002119	ORPHA:2573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2573	Moyamoya disease		HP:0100659	ORPHA:2573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0000135	ORPHA:2574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0000252	ORPHA:2574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0000407	ORPHA:2574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0000962	ORPHA:2574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0001249	ORPHA:2574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0001250	ORPHA:2574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0001596	ORPHA:2574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0004322	ORPHA:2574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0004326	ORPHA:2574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2574	Moynahan syndrome		HP:0008070	ORPHA:2574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000083	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000093	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000407	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000509	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000554	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000763	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000790	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000988	ORPHA:36412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0000989	ORPHA:36412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001250	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001251	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001287	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001315	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001369	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001373	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001541	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001654	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001698	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0001744	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002014	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002017	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002027	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002091	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002094	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002097	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002105	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002202	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002240	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002665	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002716	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002718	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0002960	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0003326	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0004374	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0004431	ORPHA:36412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0006536	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0006824	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0007400	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0009830	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0011944	ORPHA:36412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0012735	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0100021	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0100326	ORPHA:36412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0100533	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0100534	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0100665	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36412	Hypocomplementemic urticarial vasculitis		HP:0100820	ORPHA:36412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000047	ORPHA:2575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000049	ORPHA:2575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000100	ORPHA:2575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000316	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000347	ORPHA:2575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000400	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000431	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000490	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000506	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0000807	ORPHA:2575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0001249	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0001877	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0001889	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0002007	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0002014	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0002205	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0004826	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2575	Cystic fibrosis-gastritis-megaloblastic anemia syndrome		HP:0005263	ORPHA:2575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0000256	ORPHA:2576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0000431	ORPHA:2576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0001315	ORPHA:2576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0001511	ORPHA:2576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0001620	ORPHA:2576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0002240	ORPHA:2576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0002680	ORPHA:2576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0004322	ORPHA:2576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2576	Mulibrey nanism		HP:0004326	ORPHA:2576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0030521	ORPHA:95613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0030907	ORPHA:95613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000651	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000802	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000815	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000822	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000876	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0001943	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0002017	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0002315	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0002615	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0002893	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0002902	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0006824	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0008202	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0008245	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0011748	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0030591	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0030595	ORPHA:95613	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000508	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000613	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000622	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000824	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000870	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000980	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0001259	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0001945	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0002921	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0007663	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0011499	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0012378	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0040075	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0100829	ORPHA:95613	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000845	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0000863	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0001262	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0001289	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0001895	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0002339	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0003118	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95613	Pituitary apoplexy		HP:0100661	ORPHA:95613	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0000175	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0000303	ORPHA:1248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0000327	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0000457	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0000691	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0001065	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0002000	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0002650	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0003196	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0004609	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0005280	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0005288	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0008428	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0009804	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0009882	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0010185	ORPHA:1248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0010807	ORPHA:1248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0011800	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0011892	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1248	Maxillonasal dysplasia		HP:0012368	ORPHA:1248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000027	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000086	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000104	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000110	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000365	ORPHA:2578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000470	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000772	ORPHA:2578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0000813	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0002162	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0003422	ORPHA:2578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0004322	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2578	Mayer-Rokitansky-Küster-Hauser syndrome type 2		HP:0008684	ORPHA:2578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0002352	ORPHA:83629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0005871	ORPHA:83629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0000505	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0000587	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0001249	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0001258	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0001288	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0001337	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0001347	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0002059	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0002062	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0002079	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0003020	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0003487	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0004349	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0012747	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0030051	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0030866	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0100707	ORPHA:83629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0000463	ORPHA:83629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0000666	ORPHA:83629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0005280	ORPHA:83629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83629	Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome		HP:0011800	ORPHA:83629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000028	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000047	ORPHA:83628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000048	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000054	ORPHA:83628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000059	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000062	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000075	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000076	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000104	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0000136	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0001028	ORPHA:83628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0002023	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0002414	ORPHA:83628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0002475	ORPHA:83628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0002836	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0004397	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83628	LUMBAR syndrome		HP:0010609	ORPHA:83628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0000719	ORPHA:401901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0001251	ORPHA:401901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0002063	ORPHA:401901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0002072	ORPHA:401901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0002354	ORPHA:401901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0100543	ORPHA:401901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0000709	ORPHA:401901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0000716	ORPHA:401901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0000739	ORPHA:401901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0001300	ORPHA:401901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0001332	ORPHA:401901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0001337	ORPHA:401901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0002493	ORPHA:401901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401901	Huntington disease-like syndrome due to C9ORF72 expansions		HP:0001336	ORPHA:401901	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0001944	ORPHA:83620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0002013	ORPHA:83620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0002014	ORPHA:83620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0002024	ORPHA:83620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0004918	ORPHA:83620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0001409	ORPHA:83620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0002611	ORPHA:83620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0025354	ORPHA:83620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83620	Enteric anendocrinosis		HP:0100651	ORPHA:83620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000174	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000248	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000252	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000303	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000316	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000324	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000337	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000384	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000486	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000506	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000568	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000592	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000612	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000668	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0000765	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0001182	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0001250	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0001276	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0002006	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0002007	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0002558	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0002650	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0007477	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0007598	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0009748	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0010751	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0011304	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0100022	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0100267	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0100490	ORPHA:1236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0100543	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1236	Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome		HP:0100720	ORPHA:1236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0000083	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0000100	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0000988	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0001019	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0001695	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0001824	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0001880	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0001945	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0001970	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0002094	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0002113	ORPHA:139402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0002383	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0002716	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0002910	ORPHA:139402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0006515	ORPHA:139402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0006554	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0009830	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0010783	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0012115	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0012733	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0012735	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0012819	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0030249	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0100326	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0100646	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0100665	ORPHA:139402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0100827	ORPHA:139402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139402	Drug reaction with eosinophilia and systemic symptoms		HP:0200039	ORPHA:139402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000050	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000062	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000161	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000175	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000252	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0001770	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0001800	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0001883	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0006101	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0007418	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0009755	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0009756	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0010185	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0100240	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0100840	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0200102	ORPHA:1234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000160	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000347	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000430	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0000625	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0001249	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0003196	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0007957	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0009777	ORPHA:1234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0008678	ORPHA:1234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1234	Bartsocas-Papas syndrome		HP:0030680	ORPHA:1234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0000496	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0001252	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0001332	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0001336	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0001522	ORPHA:139406	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0001744	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0002069	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0002093	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0002205	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139406	Encephalopathy due to prosaposin deficiency		HP:0002240	ORPHA:139406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000049	ORPHA:1231	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000154	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000271	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000316	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000365	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000377	ORPHA:1231	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000413	ORPHA:1231	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000414	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000431	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000463	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000506	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000656	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000684	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0000974	ORPHA:1231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0001508	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0001582	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0002230	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0002557	ORPHA:1231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0008065	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0011224	ORPHA:1231	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0100783	ORPHA:1231	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0100840	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1231	Barber-Say syndrome		HP:0200102	ORPHA:1231	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0001258	ORPHA:306617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0001256	ORPHA:306617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0002342	ORPHA:306617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0002493	ORPHA:306617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0007340	ORPHA:306617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0100543	ORPHA:306617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0001181	ORPHA:306617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0001251	ORPHA:306617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306617	X-linked complicated spastic paraplegia type 1		HP:0001268	ORPHA:306617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0000044	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0000182	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0000298	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0000486	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0000544	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0001167	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0001252	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0001776	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0002342	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0002540	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0003477	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0007108	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0007209	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0008000	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2560	Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome		HP:0045037	ORPHA:2560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001513	ORPHA:2563	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000179	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000215	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000218	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000248	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000256	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000286	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000316	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000319	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000337	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000343	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000348	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000470	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000486	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000494	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000501	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000567	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000625	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000639	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000679	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000684	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000689	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000879	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000965	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001176	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001249	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001250	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001520	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001548	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001795	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0001833	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0002007	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0002980	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0004322	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0007633	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0008577	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0011849	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0012810	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0025112	ORPHA:2563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000098	ORPHA:2563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000618	ORPHA:2563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0000717	ORPHA:2563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome		HP:0006585	ORPHA:2563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2563	MOMO syndrome	NOT	HP:0000820	ORPHA:2563	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2564	Tetramelic monodactyly		HP:0001171	ORPHA:2564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2564	Tetramelic monodactyly		HP:0012165	ORPHA:2564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0000028	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0000347	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0000358	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0000414	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0000431	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0002002	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0002093	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0011001	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0030680	ORPHA:1237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0000062	ORPHA:1237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0001252	ORPHA:1237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0001334	ORPHA:1237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1237	Beemer-Ertbruggen syndrome		HP:0001873	ORPHA:1237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664372	Soft and hard cleft palate		HP:0000327	ORPHA:664372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664372	Soft and hard cleft palate		HP:0000689	ORPHA:664372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664372	Soft and hard cleft palate		HP:0001611	ORPHA:664372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664372	Soft and hard cleft palate		HP:0000347	ORPHA:664372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401911	AXIN2-related polyposis		HP:0005227	ORPHA:401911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401911	AXIN2-related polyposis		HP:0200063	ORPHA:401911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401911	AXIN2-related polyposis		HP:0003003	ORPHA:401911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401911	AXIN2-related polyposis		HP:0100743	ORPHA:401911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401911	AXIN2-related polyposis	NOT	HP:0000968	ORPHA:401911	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:401911	AXIN2-related polyposis	NOT	HP:0008070	ORPHA:401911	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:401911	AXIN2-related polyposis	NOT	HP:3000050	ORPHA:401911	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0000154	ORPHA:83619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0000316	ORPHA:83619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0000384	ORPHA:83619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0000508	ORPHA:83619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0000602	ORPHA:83619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0004467	ORPHA:83619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0011272	ORPHA:83619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83619	Macrostomia-preauricular tags-external ophthalmoplegia syndrome		HP:0011338	ORPHA:83619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0000083	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0000505	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0000509	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0000613	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0000621	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0000795	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001637	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001645	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001658	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001733	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001824	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001873	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001874	ORPHA:36426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001903	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001945	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0001960	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002014	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002015	ORPHA:36426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002017	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002027	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002043	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002091	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002094	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002103	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002205	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002239	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0002910	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0003781	ORPHA:36426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0006554	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0008066	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0010783	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0012378	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0012733	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0012735	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0030016	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0100518	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0100792	ORPHA:36426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0100806	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36426	Stevens-Johnson syndrome		HP:0200020	ORPHA:36426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0010976	ORPHA:83617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000175	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000252	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000347	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000369	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000430	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000452	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000581	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001036	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001051	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001166	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001263	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001508	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002098	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002850	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0004440	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0008897	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0011471	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0025092	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0031190	ORPHA:83617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000023	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000028	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000054	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000126	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000160	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000244	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000278	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000286	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000348	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000431	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000494	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000883	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000890	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000954	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000964	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0000989	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001081	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001344	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001511	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0001845	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002021	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002089	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002208	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002240	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002506	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002594	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0002949	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0004425	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0004616	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0010976	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0006560	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0009697	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0011682	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83617	Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome		HP:0012444	ORPHA:83617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000219	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000252	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000322	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000331	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000358	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000430	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001256	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001488	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001763	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001863	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0004322	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0009237	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0011833	ORPHA:163979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000028	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000047	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000054	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000126	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000175	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000238	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000337	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000453	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000494	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000520	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0000582	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001187	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001321	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001629	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001631	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001643	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001782	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001838	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001873	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0001903	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0002093	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0002170	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0002682	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0002777	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0002901	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0002904	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0004691	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0005306	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0006610	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0008386	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0008551	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0010511	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0011467	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0011611	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163979	X-linked intellectual disability-craniofacioskeletal syndrome		HP:0030148	ORPHA:163979	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0002121	ORPHA:139431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0011168	ORPHA:139431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0002123	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0010852	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0010858	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0011185	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0011193	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0020216	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0025190	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0045084	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0100785	ORPHA:139431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0000739	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0001249	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0001328	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0002373	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0002457	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0007704	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0010819	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0010850	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0011182	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0012001	ORPHA:139431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0010818	ORPHA:139431	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139431	Epilepsy with eyelid myoclonia		HP:0031491	ORPHA:139431	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000239	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000244	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000248	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000520	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0009380	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0001510	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0001531	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0002007	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0004322	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0006501	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0009601	ORPHA:1225	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000160	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000218	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0001191	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0001511	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0001545	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0002024	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0003196	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0005916	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0006487	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0006498	ORPHA:1225	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000069	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000076	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000126	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000175	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000275	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000286	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000316	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000337	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000347	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000405	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000426	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000446	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000601	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0000639	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0001029	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0001671	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0002023	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0002650	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0002665	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0002669	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0100542	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1225	Baller-Gerold syndrome		HP:0100589	ORPHA:1225	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000486	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000639	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0001249	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0001263	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0001328	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0001387	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0002300	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0002381	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0002984	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0003022	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0003042	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0003196	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0003510	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0007957	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0010529	ORPHA:2557	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000348	ORPHA:2557	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000431	ORPHA:2557	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000445	ORPHA:2557	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0003070	ORPHA:2557	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0004209	ORPHA:2557	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000252	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000482	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000518	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0000647	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0001385	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0001840	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0001883	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0002673	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0002812	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0002827	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0002991	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2557	Mietens syndrome		HP:0005743	ORPHA:2557	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139436	Multicentric reticulohistiocytosis		HP:0001324	ORPHA:139436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139436	Multicentric reticulohistiocytosis		HP:0001369	ORPHA:139436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139436	Multicentric reticulohistiocytosis		HP:0001945	ORPHA:139436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139436	Multicentric reticulohistiocytosis		HP:0004326	ORPHA:139436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139436	Multicentric reticulohistiocytosis		HP:0100727	ORPHA:139436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139436	Multicentric reticulohistiocytosis		HP:0200036	ORPHA:139436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0001276	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0002267	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0002376	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0002384	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0007333	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0010818	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0012018	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0200134	ORPHA:163985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163985	Hyperekplexia-epilepsy syndrome		HP:0000243	ORPHA:163985	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0000117	ORPHA:352540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0001324	ORPHA:352540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002148	ORPHA:352540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002756	ORPHA:352540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0003109	ORPHA:352540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0003155	ORPHA:352540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0000121	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002653	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002659	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002749	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0003701	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0006487	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0010622	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0012052	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:6000489	ORPHA:352540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0000768	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0000787	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0001288	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0001510	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0001760	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0001850	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002093	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002669	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002808	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002823	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002901	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002982	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0002991	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0004912	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0010734	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0011847	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0012288	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0040163	ORPHA:352540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0003468	ORPHA:352540	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352540	Oncogenic osteomalacia		HP:0030731	ORPHA:352540	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1221	Cheilitis glandularis		HP:0000179	ORPHA:1221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1221	Cheilitis glandularis		HP:0002664	ORPHA:1221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1221	Cheilitis glandularis		HP:0002860	ORPHA:1221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1221	Cheilitis glandularis		HP:0010286	ORPHA:1221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1221	Cheilitis glandularis		HP:0010978	ORPHA:1221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001824	ORPHA:2552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002027	ORPHA:2552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002028	ORPHA:2552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002254	ORPHA:2552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002721	ORPHA:2552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0032218	ORPHA:2552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000246	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001945	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002013	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002018	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002039	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0011277	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0012384	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0012387	ORPHA:2552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000024	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000123	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000206	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000491	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000572	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000828	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0000849	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001080	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001096	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001250	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001733	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001743	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0001944	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002090	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002383	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002586	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002754	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002778	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0002840	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0004326	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0005561	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0008777	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0011027	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0011950	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0012115	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0012804	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0012819	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0025439	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0030049	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0030126	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0030151	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0100584	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0100614	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0100646	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0100806	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0200036	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2552	Microsporidiosis		HP:0500006	ORPHA:2552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1229	Congenital intrauterine infection-like syndrome		HP:0000252	ORPHA:1229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1229	Congenital intrauterine infection-like syndrome		HP:0001250	ORPHA:1229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1229	Congenital intrauterine infection-like syndrome		HP:0001257	ORPHA:1229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1229	Congenital intrauterine infection-like syndrome		HP:0001347	ORPHA:1229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1229	Congenital intrauterine infection-like syndrome		HP:0002120	ORPHA:1229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1229	Congenital intrauterine infection-like syndrome		HP:0002514	ORPHA:1229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1229	Congenital intrauterine infection-like syndrome		HP:0100022	ORPHA:1229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1228	Banki syndrome		HP:0001156	ORPHA:1228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1228	Banki syndrome		HP:0004209	ORPHA:1228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1228	Banki syndrome		HP:0005048	ORPHA:1228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1228	Banki syndrome		HP:0005916	ORPHA:1228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000028	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000160	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000252	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000278	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000347	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000356	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000413	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001508	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001510	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001511	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0002750	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0003100	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0003510	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0004209	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001382	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0005930	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0009892	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0009939	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0011267	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0011968	ORPHA:2554	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000059	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000060	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000064	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000327	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000358	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000369	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000772	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001363	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0002094	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0002098	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0002705	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0002878	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0006443	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0006660	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0008665	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0100490	ORPHA:2554	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000039	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000047	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000175	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000176	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000193	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0000365	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001249	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001263	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0001328	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0003042	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0008736	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0012471	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2554	Ear-patella-short stature syndrome		HP:0100783	ORPHA:2554	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000035	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000147	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000164	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000252	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000275	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000340	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000444	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000490	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000821	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000828	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0000842	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0001249	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0001250	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0001251	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0001511	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0002353	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0003118	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0004097	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0004322	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0008193	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1227	Bangstad syndrome		HP:0100651	ORPHA:1227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0000175	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0000278	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0000453	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0000851	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0001249	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0001561	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0008191	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1226	Bamforth-Lazarus syndrome		HP:0011362	ORPHA:1226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000528	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000568	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000647	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000776	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000953	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001000	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0004334	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0007957	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0008065	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0010783	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0011800	ORPHA:2556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000278	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000347	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000431	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000445	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000492	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000499	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000598	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000614	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001053	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001639	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001644	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001671	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001999	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0003510	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0004327	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0007703	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0009939	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0011531	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0011675	ORPHA:2556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000035	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000036	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000037	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000039	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000047	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000062	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000238	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000252	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000363	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000365	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000501	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000556	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000572	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000618	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000627	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000646	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000682	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0000960	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001249	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001250	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001263	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001274	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001328	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001331	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001508	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001510	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001597	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001634	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001653	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0001704	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0002034	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0002094	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0002098	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0002133	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0002300	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0002381	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0002878	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0004302	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0004378	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0005180	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0007731	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0007973	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0008665	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0010529	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0011027	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0011265	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2556	Microphthalmia with linear skin defects syndrome		HP:0011968	ORPHA:2556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0000988	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0000989	ORPHA:37748	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0001025	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0001369	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0001744	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0001903	ORPHA:37748	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0001945	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0001974	ORPHA:37748	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0002240	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0002633	ORPHA:37748	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0002653	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0002665	ORPHA:37748	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0002716	ORPHA:37748	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0002829	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0003326	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0003496	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0009830	ORPHA:37748	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0011001	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0012378	ORPHA:37748	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0012733	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37748	Schnitzler syndrome		HP:0200034	ORPHA:37748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000174	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000219	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000431	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000486	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000494	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000577	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000687	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000750	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0001156	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0001252	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0001263	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0011078	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0011220	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0031936	ORPHA:477993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000028	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000041	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000047	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000256	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000316	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000463	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000592	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000657	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000664	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0000998	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0001182	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0001488	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0001655	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0001800	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0002079	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0002169	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0002209	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0002558	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0004209	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0006895	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0009778	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0009890	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0011832	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0012081	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0012430	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0012448	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0030048	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477993	Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome		HP:0045075	ORPHA:477993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0000303	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0000455	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0000470	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0000894	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0001182	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0001256	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0001644	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0001647	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0001659	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0001999	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0002553	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0002947	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0003124	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0004322	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0005978	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0011342	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0011822	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0012368	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0025502	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0100817	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0100874	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401923	9q31.1q31.3 microdeletion syndrome		HP:0200055	ORPHA:401923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0005318	ORPHA:83601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0000821	ORPHA:83601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0000853	ORPHA:83601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0001289	ORPHA:83601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0002500	ORPHA:83601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0002902	ORPHA:83601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0003470	ORPHA:83601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0000709	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0000716	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0000739	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0001873	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0001945	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0001974	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0002017	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0002133	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0002197	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0002315	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0002721	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0007359	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0009102	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0012332	ORPHA:83601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0005991	ORPHA:83601	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis	NOT	HP:0002181	ORPHA:83601	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0006846	ORPHA:83601	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:83601	Steroid-responsive encephalopathy associated with autoimmune thyroiditis		HP:0000872	ORPHA:83601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001298	ORPHA:83600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0002360	ORPHA:83600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0000651	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001254	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001268	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001300	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001337	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001945	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0002315	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0002922	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0002960	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0003326	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0003484	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0004429	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0005986	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0007146	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0010702	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0012547	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0025439	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0100660	ORPHA:83600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0000020	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0000613	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0000709	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001250	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001259	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0001662	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0002607	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0002883	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0009763	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83600	Encephalitis lethargica		HP:0025258	ORPHA:83600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0007404	ORPHA:530838	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0007447	ORPHA:530838	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0000958	ORPHA:530838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0001551	ORPHA:530838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0010783	ORPHA:530838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0012203	ORPHA:530838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0001047	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0001598	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0004690	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0006203	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0007446	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0025524	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0032523	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0032541	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530838	KRT1-related diffuse nonepidermolytic keratoderma		HP:0040189	ORPHA:530838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0000277	ORPHA:1214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0000324	ORPHA:1214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0000347	ORPHA:1214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0007400	ORPHA:1214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0001250	ORPHA:1214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0003011	ORPHA:1214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0008065	ORPHA:1214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0100555	ORPHA:1214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0000490	ORPHA:1214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0000508	ORPHA:1214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1214	Progressive hemifacial atrophy		HP:0001100	ORPHA:1214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000219	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000248	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000252	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000286	ORPHA:352530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000311	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000316	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000341	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000377	ORPHA:352530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000431	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000664	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0001263	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0000851	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0001182	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0001250	ORPHA:352530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0001252	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0001321	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0001513	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0001999	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0002047	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0002079	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0002120	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0002123	ORPHA:352530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0002265	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0002714	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0004209	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0009891	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0007052	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0010864	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0007642	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0011228	ORPHA:352530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome		HP:0012443	ORPHA:352530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0000014	ORPHA:2547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0000072	ORPHA:2547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0000347	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0000568	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0001376	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0001561	ORPHA:2547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0001643	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0002007	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0003196	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0008551	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0008736	ORPHA:2547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0009773	ORPHA:2547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0010935	ORPHA:2547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0100490	ORPHA:2547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2547	Microphthalmia-microtia-fetal akinesia syndrome		HP:0100867	ORPHA:2547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000324	ORPHA:2549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000359	ORPHA:2549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0003778	ORPHA:2549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0006511	ORPHA:2549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0008551	ORPHA:2549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0009601	ORPHA:2549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0030680	ORPHA:2549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000076	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000202	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000384	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000407	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000413	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0003458	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0004322	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0004452	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0004467	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0006695	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0008678	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0008706	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0100543	ORPHA:2549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000078	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000154	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000175	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0000405	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0001177	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0001199	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0004397	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0006703	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0008056	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0009800	ORPHA:2549	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:2549	Oculoauriculovertebral spectrum with radial defects		HP:0100335	ORPHA:2549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0002069	ORPHA:139426	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0010850	ORPHA:139426	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0002371	ORPHA:139426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0004372	ORPHA:139426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0011168	ORPHA:139426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0012462	ORPHA:139426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0001249	ORPHA:139426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0002121	ORPHA:139426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0002123	ORPHA:139426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139426	Perioral myoclonia with absences		HP:0002527	ORPHA:139426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1216	Autosomal dominant congenital benign spinal muscular atrophy		HP:0001252	ORPHA:1216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1216	Autosomal dominant congenital benign spinal muscular atrophy		HP:0001387	ORPHA:1216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1216	Autosomal dominant congenital benign spinal muscular atrophy		HP:0003693	ORPHA:1216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1216	Autosomal dominant congenital benign spinal muscular atrophy		HP:0004326	ORPHA:1216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1216	Autosomal dominant congenital benign spinal muscular atrophy		HP:0008964	ORPHA:1216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0000529	ORPHA:1215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0000648	ORPHA:1215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0000407	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0000590	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0000649	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0001488	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0003198	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0003325	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0003737	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0004463	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0012378	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0020119	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0100285	ORPHA:1215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0000763	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0001133	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0001251	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0001258	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0001761	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0003438	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0003444	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0007002	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0009830	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0012511	ORPHA:1215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0000819	ORPHA:1215	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0001638	ORPHA:1215	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1215	Autosomal dominant optic atrophy plus syndrome		HP:0002076	ORPHA:1215	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000218	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000233	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000248	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000252	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000294	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000343	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000347	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000413	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000463	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000470	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000527	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000574	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000664	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000684	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000687	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001249	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001276	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001770	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001773	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002020	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002162	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002230	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002553	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002714	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002750	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002983	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0003196	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0004322	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0005280	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0007665	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0009623	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0010034	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0010300	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0010864	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0200055	ORPHA:199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000003	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000028	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000047	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000059	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000076	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000358	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000405	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000407	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000482	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000498	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000508	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000545	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000667	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000722	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000739	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000965	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001387	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001508	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001511	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001622	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002167	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002360	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002557	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002974	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0003042	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0004209	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0007018	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0007598	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0008736	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0008850	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0008872	ORPHA:199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000083	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000130	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000175	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000400	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000453	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000486	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000501	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000518	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000639	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000717	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000767	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000776	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000786	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0000823	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001250	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001252	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001385	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001557	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001629	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001631	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001883	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0001956	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002021	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002119	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002120	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002566	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002580	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0002827	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0007360	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0009830	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0010880	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0012165	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0030680	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:199	Cornelia de Lange syndrome		HP:0040071	ORPHA:199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000384	ORPHA:195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0002023	ORPHA:195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0004467	ORPHA:195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000126	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000316	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000494	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000567	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000612	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000772	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0001252	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0001256	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0001385	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0001511	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0004322	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0008678	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0030680	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0100542	ORPHA:195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000078	ORPHA:195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000365	ORPHA:195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:195	Cat-eye syndrome		HP:0000568	ORPHA:195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000239	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000270	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000271	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000929	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000974	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001249	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001263	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001328	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002514	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001382	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0100777	ORPHA:198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000343	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000767	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000768	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000926	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000938	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000939	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000952	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000978	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000987	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001156	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001252	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001396	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002015	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002020	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002033	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002036	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002045	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002578	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002617	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002705	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002748	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002749	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0003019	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0004279	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0004408	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0005293	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0010562	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0012115	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0025270	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0100240	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0100633	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0100699	ORPHA:198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000010	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000015	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000023	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000348	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000494	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0000774	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001385	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0001763	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002208	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002650	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002673	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002797	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002808	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002812	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002827	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002857	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0002991	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0003172	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0003874	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0005743	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0006507	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0006660	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0008818	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0009556	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0100541	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0100874	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:198	Occipital horn syndrome		HP:0200021	ORPHA:198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000179	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000194	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000232	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000280	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000286	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000316	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000463	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000494	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000668	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000687	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000767	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000768	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000940	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001176	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001182	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001249	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001252	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001500	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002007	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002167	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002650	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002750	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002808	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0003312	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0004322	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0004493	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0005280	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001382	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0006482	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0009928	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0011344	ORPHA:192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000154	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000189	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000218	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000252	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000327	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000411	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000445	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001276	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001288	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001582	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001763	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001804	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001812	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002119	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002191	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002868	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0006480	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0006692	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0008872	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0008897	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0009193	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0009882	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0010049	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0011065	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0011220	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0011580	ORPHA:192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000023	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000407	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000486	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000518	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000648	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000684	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0000708	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001250	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001324	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001633	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001638	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001646	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0001702	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002120	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002269	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0002711	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0003202	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0006288	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0007360	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0007370	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0007703	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0010535	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0010819	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:192	Coffin-Lowry syndrome		HP:0100716	ORPHA:192	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0000099	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0001824	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0001945	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002039	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002829	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0003326	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0005368	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0010876	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0011123	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0011227	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0012649	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0030166	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0031691	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0032018	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0200029	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0410008	ORPHA:48435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0000093	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0000790	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0000793	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0000822	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0000965	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0001063	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0001369	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0001482	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0001638	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002011	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002027	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002090	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002140	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002617	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002726	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0002923	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0003261	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0003493	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0004386	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0005318	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0005366	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0005401	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0006562	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0006689	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0009830	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0010702	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0011274	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0020101	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0020114	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0020180	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0025143	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0025188	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0030880	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0031363	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0031692	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0031693	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0032166	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0032170	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0032230	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0100778	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48435	Postinfectious vasculitis		HP:0100796	ORPHA:48435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139450	Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome		HP:0000564	ORPHA:139450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139450	Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome		HP:0000612	ORPHA:139450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139450	Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome		HP:0000613	ORPHA:139450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139450	Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome		HP:0008551	ORPHA:139450	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0003477	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0004934	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0005930	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0006482	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0006483	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0008043	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0008197	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0008936	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0011451	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0011471	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0011527	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0012211	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0012804	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0025300	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0025403	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000568	ORPHA:191	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000573	ORPHA:191	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001105	ORPHA:191	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001344	ORPHA:191	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0006349	ORPHA:191	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000253	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000408	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000580	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000708	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001268	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001272	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001510	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0003510	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0004326	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0007266	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0007703	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0008897	ORPHA:191	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000490	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000518	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000529	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000556	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000670	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000762	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000992	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001250	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001251	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001263	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001288	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001757	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002020	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002059	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002135	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002171	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002213	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002461	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002514	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002545	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002803	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0003202	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0003474	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0003758	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0005781	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0006297	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0007108	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0007141	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0007240	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0007346	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0008872	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0009830	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0011359	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0012372	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0100543	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0100678	ORPHA:191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000011	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000020	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000028	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000083	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000089	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000093	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000100	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000122	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000444	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000481	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000486	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000512	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000519	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000522	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000540	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000543	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000546	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000585	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000613	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000616	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000633	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000639	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000648	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000680	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000689	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000819	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000822	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000823	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0000970	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001097	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001249	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001257	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001265	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001276	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001284	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001347	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001612	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001744	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002080	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002149	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002240	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002345	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0001288	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002376	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002509	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002540	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002621	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002650	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002684	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002808	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:191	Cockayne syndrome		HP:0002910	ORPHA:191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000219	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000316	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000494	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0001156	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0001256	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0001382	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0001627	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0009778	ORPHA:401935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000028	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000086	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000319	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000343	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000426	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000431	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0000664	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0001629	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0001631	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0001660	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0002566	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0003083	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0003196	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0004935	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0005852	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401935	14q24.1q24.3 microdeletion syndrome		HP:0011800	ORPHA:401935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000028	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000164	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000194	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000212	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000252	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000294	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000322	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000327	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000347	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000384	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000407	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000426	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000486	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000492	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000494	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000499	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000527	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000545	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000568	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000574	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000612	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000639	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000648	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000767	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0000823	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001000	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001135	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001166	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001182	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001249	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001250	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001252	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001263	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001511	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001513	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001531	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001558	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001572	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001612	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001629	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001634	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001852	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001875	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0002167	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0002650	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0002705	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0002808	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0002857	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0002967	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0003272	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0004209	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0004283	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0004322	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0001382	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0006101	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0007703	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0008872	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0009804	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0009906	ORPHA:193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0010295	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0010669	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0011308	ORPHA:193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0100874	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:193	Cohen syndrome		HP:0200046	ORPHA:193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000518	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000568	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000639	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000763	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0001256	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0001263	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0001511	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0002808	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0003134	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0003401	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0004322	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0005830	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0007182	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0010620	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0034681	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000939	ORPHA:48431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0002120	ORPHA:48431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0002650	ORPHA:48431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0030890	ORPHA:48431	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0001251	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0001310	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0001943	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0002072	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0002080	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0002119	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0003319	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0007256	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0008942	ORPHA:48431	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000044	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000347	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000482	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48431	Congenital cataracts-facial dysmorphism-neuropathy syndrome		HP:0000486	ORPHA:48431	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0000486	ORPHA:190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0000501	ORPHA:190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0000518	ORPHA:190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0000541	ORPHA:190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0000593	ORPHA:190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0001103	ORPHA:190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0008046	ORPHA:190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:190	Coats disease		HP:0008053	ORPHA:190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0001561	ORPHA:1203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0002247	ORPHA:1203	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0001622	ORPHA:1203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0002013	ORPHA:1203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0025656	ORPHA:1203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0001508	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0001732	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0001734	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0001824	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0001944	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0002587	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0003270	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0004414	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0004909	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0030145	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1203	Duodenal atresia		HP:0034754	ORPHA:1203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1202	Larynx atresia		HP:0001601	ORPHA:1202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1202	Larynx atresia		HP:0001608	ORPHA:1202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1202	Larynx atresia		HP:0002093	ORPHA:1202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1202	Larynx atresia		HP:0002205	ORPHA:1202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1202	Larynx atresia		HP:0004322	ORPHA:1202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1202	Larynx atresia		HP:0030680	ORPHA:1202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0000286	ORPHA:2536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0000311	ORPHA:2536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0000482	ORPHA:2536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0000501	ORPHA:2536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0000505	ORPHA:2536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0000929	ORPHA:2536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0000982	ORPHA:2536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0002688	ORPHA:2536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0012368	ORPHA:2536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2536	Microcornea-glaucoma-absent frontal sinuses syndrome		HP:0100789	ORPHA:2536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0004322	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0005235	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0011968	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0025015	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0005245	ORPHA:1201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0001508	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0001511	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0002013	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0002566	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1201	Small bowel atresia		HP:0003270	ORPHA:1201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0000174	ORPHA:1200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0000316	ORPHA:1200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0000426	ORPHA:1200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0000431	ORPHA:1200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0000478	ORPHA:1200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0000504	ORPHA:1200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0001671	ORPHA:1200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0003196	ORPHA:1200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0004322	ORPHA:1200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0004502	ORPHA:1200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1200	Burn-McKeown syndrome		HP:0012745	ORPHA:1200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001508	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001510	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001743	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002020	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002036	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002818	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0009778	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0011968	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0100633	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0100841	ORPHA:2538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0000003	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0000110	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001167	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001357	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002007	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0031095	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0005916	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0005988	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0011220	ORPHA:2538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0000085	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0000104	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0000143	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0000528	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0000568	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001274	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001331	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001631	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0001660	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002023	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002032	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002101	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002139	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002240	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002536	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002566	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0002575	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0003042	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0004050	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0004736	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0004871	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0006660	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0008678	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0009827	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0009829	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0012165	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0025023	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0030680	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2538	Microgastria-limb reduction defect syndrome		HP:0100257	ORPHA:2538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0001260	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0001269	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0001290	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0001300	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0001332	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0001337	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0002067	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0006801	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0006956	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0011331	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0012444	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0012768	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0100556	ORPHA:306669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0000716	ORPHA:306669	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0001288	ORPHA:306669	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0002650	ORPHA:306669	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306669	Hemiparkinsonism-hemiatrophy syndrome		HP:0100308	ORPHA:306669	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001999	ORPHA:488642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0002141	ORPHA:488642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0010864	ORPHA:488642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0011344	ORPHA:488642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0011451	ORPHA:488642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000365	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001156	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001250	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001257	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001344	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0002465	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0002540	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0004322	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0004692	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0008947	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0011968	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0030084	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0030962	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0100022	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0100704	ORPHA:488642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000081	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000175	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000308	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000316	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000510	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000519	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000582	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000592	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0000768	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001182	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001251	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001276	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001382	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001511	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001583	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001734	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001773	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001800	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001838	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0001845	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0002714	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0002751	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0003273	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0004209	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0006380	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0006979	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0007598	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0008513	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0008780	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0010296	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0020045	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488642	TELO2-related intellectual disability-neurodevelopmental disorder		HP:0200055	ORPHA:488642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0011662	ORPHA:1209	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0000961	ORPHA:1209	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0001629	ORPHA:1209	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0001631	ORPHA:1209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0001655	ORPHA:1209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0001669	ORPHA:1209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0004762	ORPHA:1209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0005301	ORPHA:1209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0001680	ORPHA:1209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1209	Tricuspid atresia		HP:0004935	ORPHA:1209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1208	Pulmonary atresia-intact ventricular septum syndrome		HP:0001622	ORPHA:1208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1208	Pulmonary atresia-intact ventricular septum syndrome		HP:0001643	ORPHA:1208	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1208	Pulmonary atresia-intact ventricular septum syndrome		HP:0001702	ORPHA:1208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1208	Pulmonary atresia-intact ventricular septum syndrome		HP:0004935	ORPHA:1208	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1208	Pulmonary atresia-intact ventricular septum syndrome		HP:0009800	ORPHA:1208	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0003764	ORPHA:35125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0000953	ORPHA:35125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0001010	ORPHA:35125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0002176	ORPHA:35125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0003416	ORPHA:35125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0006827	ORPHA:35125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0007199	ORPHA:35125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0012531	ORPHA:35125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0000483	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0000505	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0000750	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0001263	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0001276	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0001284	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0002944	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0003487	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0009077	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0010302	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0012032	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0012443	ORPHA:35125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0000113	ORPHA:35125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0000938	ORPHA:35125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0001999	ORPHA:35125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0002859	ORPHA:35125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0004942	ORPHA:35125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35125	Epidermal nevus syndrome		HP:0100512	ORPHA:35125	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0002014	ORPHA:35122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0002027	ORPHA:35122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0002013	ORPHA:35122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0002018	ORPHA:35122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0002019	ORPHA:35122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0002020	ORPHA:35122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0004396	ORPHA:35122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0033589	ORPHA:35122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0002607	ORPHA:35122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0003270	ORPHA:35122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0011848	ORPHA:35122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0012378	ORPHA:35122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0025085	ORPHA:35122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35122	Congenital sucrase-isomaltase deficiency		HP:0001508	ORPHA:35122	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000174	ORPHA:2533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000232	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000252	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000286	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000324	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000347	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000369	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000378	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000384	ORPHA:2533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000407	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0000411	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0001249	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0002057	ORPHA:2533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0002167	ORPHA:2533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2533	Microcephaly-deafness-intellectual disability syndrome		HP:0004322	ORPHA:2533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0000708	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0001260	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002015	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002059	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002071	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002376	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0007256	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0030890	ORPHA:500180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0000252	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0001250	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0001257	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0001263	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0001332	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0001344	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002066	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002187	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002353	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002381	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002540	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0010864	ORPHA:500180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0000718	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0000729	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0000752	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0000768	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002072	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002079	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002119	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002509	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0002808	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0007328	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0008947	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0011471	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500180	Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder		HP:0100710	ORPHA:500180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0000653	ORPHA:189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0000972	ORPHA:189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0000982	ORPHA:189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0001596	ORPHA:189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0008070	ORPHA:189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0008404	ORPHA:189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0045075	ORPHA:189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0000365	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0000953	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0001072	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0001792	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0001798	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0002209	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0002213	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0002215	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0002221	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0002223	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0002225	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0002555	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0004528	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0004779	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0005599	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0008383	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0011911	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0031288	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0045059	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189	Hidrotic ectodermal dysplasia		HP:0100759	ORPHA:189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0001974	ORPHA:188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0010741	ORPHA:188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0001733	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0001824	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0002014	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0002027	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0002615	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0003326	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0012378	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0025142	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0031417	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0100598	ORPHA:188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0000083	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0000091	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0001701	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0002202	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0004936	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0006543	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0006775	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0011675	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0012735	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0012819	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:188	Systemic capillary leak syndrome		HP:0100520	ORPHA:188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001627	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001629	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001631	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001635	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001651	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001680	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0002088	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0002089	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0004971	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0005345	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0030680	ORPHA:185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001636	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001643	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001719	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001750	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0002092	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0002098	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0002205	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0004383	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0010772	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0010773	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0011560	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0012382	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0012735	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0025495	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0040044	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0040045	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0100632	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0100730	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0100790	ORPHA:185	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0000119	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0000925	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0001660	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0002107	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0011638	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0011662	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0011670	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0011671	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:185	Scimitar syndrome		HP:0012722	ORPHA:185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000164	ORPHA:184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000277	ORPHA:184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000293	ORPHA:184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000505	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000520	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000529	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000648	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0000677	ORPHA:184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0001608	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0002781	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0002870	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0006482	ORPHA:184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0008872	ORPHA:184	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0012062	ORPHA:184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:184	Cherubism		HP:0012802	ORPHA:184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0000161	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0000204	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0000277	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0000309	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0000326	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0000699	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0010281	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0012292	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:0040079	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401942	Familial median cleft of the upper and lower lips		HP:3000010	ORPHA:401942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0000953	ORPHA:186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001394	ORPHA:186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002613	ORPHA:186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002908	ORPHA:186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0011971	ORPHA:186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0030167	ORPHA:186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0000820	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0000952	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0000989	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001114	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001278	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001395	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001399	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001402	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001409	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002240	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002841	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002960	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003119	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003124	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003155	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003493	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003496	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0011040	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0012203	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0030948	ORPHA:186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0000939	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001262	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001541	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0001744	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002040	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002360	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002480	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002570	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0002608	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003073	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003261	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0003270	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0012115	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0012378	ORPHA:186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:186	Primary biliary cholangitis		HP:0004386	ORPHA:186	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000175	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000176	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000193	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000252	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000278	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000347	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001249	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001257	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001274	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001276	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001331	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001508	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001510	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001511	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002063	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0003510	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0003552	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0011968	ORPHA:35107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000160	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000363	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000366	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000358	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000369	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000486	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000639	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001250	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002119	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002133	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0003196	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0005280	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0009748	ORPHA:35107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000062	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000104	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000238	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000256	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000286	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0000494	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001302	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001339	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001643	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001744	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001840	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001883	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002007	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002126	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002269	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002536	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002566	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0002983	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0004334	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0001302	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0008065	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0008678	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0010772	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0011001	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0011002	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35107	Desmosterolosis		HP:0011220	ORPHA:35107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0000232	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0000457	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0000684	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0000691	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0000966	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0002231	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0008070	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0010803	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0100840	ORPHA:181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0002007	ORPHA:181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0000822	ORPHA:181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0000830	ORPHA:181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0009882	ORPHA:181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:181	X-linked hypohidrotic ectodermal dysplasia		HP:0100651	ORPHA:181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0000505	ORPHA:180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0000512	ORPHA:180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0000545	ORPHA:180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0000662	ORPHA:180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0007703	ORPHA:180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0000529	ORPHA:180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0001133	ORPHA:180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0001139	ORPHA:180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0007994	ORPHA:180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0000533	ORPHA:180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0000551	ORPHA:180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0007787	ORPHA:180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0011506	ORPHA:180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0030602	ORPHA:180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180	Choroideremia		HP:0040049	ORPHA:180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000246	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000979	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001025	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001824	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001880	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002099	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002113	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002633	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002960	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0007009	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0009830	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0012649	ORPHA:183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000790	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000822	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000988	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001053	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001288	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001639	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001697	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001970	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002015	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002017	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002027	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002103	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002829	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002923	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0003212	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0004936	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0006536	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0012378	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0032018	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0032071	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0032230	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0033557	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0033559	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0034104	ORPHA:183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000083	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000093	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0000965	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001063	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001369	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001482	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001635	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001658	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0001945	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002020	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002024	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002093	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002105	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002202	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0002326	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0003326	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0004374	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0005214	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0006535	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0006824	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0008653	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0012735	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0012819	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0032064	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0100582	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0100584	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0100614	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0100820	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:0200034	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:183	Eosinophilic granulomatosis with polyangiitis		HP:6000070	ORPHA:183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0001297	ORPHA:401945	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0000822	ORPHA:401945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0011834	ORPHA:401945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0100659	ORPHA:401945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0000965	ORPHA:401945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0001873	ORPHA:401945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0030402	ORPHA:401945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401945	Moyamoya disease with early-onset achalasia		HP:0030880	ORPHA:401945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0000989	ORPHA:182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0002814	ORPHA:182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0000962	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0000969	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0001004	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0001482	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0001760	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0003550	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0012500	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0025474	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0025475	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0025527	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0025528	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0040009	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0045059	ORPHA:182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0000987	ORPHA:182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0001053	ORPHA:182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0002718	ORPHA:182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0002817	ORPHA:182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0011276	ORPHA:182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0031842	ORPHA:182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0000163	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0000491	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0000656	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0001097	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0002088	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0002721	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0002797	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0002860	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0007606	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0011334	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0031013	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:182	Chromomycosis		HP:0500043	ORPHA:182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0001250	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0001266	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0001320	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0001321	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002123	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002360	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0006850	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0011344	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0011968	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0031162	ORPHA:2524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0000253	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0000340	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0001270	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002020	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002033	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002104	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002268	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002365	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002719	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0007663	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0012469	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0200136	ORPHA:2524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0001257	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002079	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002119	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002536	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0003487	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0003558	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0006895	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0006989	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0007598	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0008936	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0011171	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0011471	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0012765	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0025190	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0100704	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0200049	ORPHA:2524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2		HP:0002350	ORPHA:2524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2524	Pontocerebellar hypoplasia type 2	NOT	HP:0001999	ORPHA:2524	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0001249	ORPHA:139444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0001263	ORPHA:139444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0001270	ORPHA:139444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0002061	ORPHA:139444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0002352	ORPHA:139444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0010576	ORPHA:139444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0000252	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0000407	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0000486	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0001344	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0002169	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0003487	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0004302	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139444	Leukoencephalopathy with bilateral anterior temporal lobe cysts		HP:0008936	ORPHA:139444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0007731	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0007973	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0009891	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0010310	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0012471	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0012490	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0040189	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0100658	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0100758	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0200042	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000252	ORPHA:2526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000478	ORPHA:2526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000504	ORPHA:2526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001004	ORPHA:2526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000545	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000969	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001249	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001252	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001263	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001328	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001595	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001820	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0007703	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0008388	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0100644	ORPHA:2526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000286	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000293	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000307	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000340	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000343	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000411	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000431	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000445	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000463	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000488	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000492	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000499	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000501	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000508	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000518	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000528	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000541	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000556	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000568	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000572	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000582	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000587	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000614	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000618	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000646	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000648	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0000958	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001055	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001072	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001250	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001257	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001276	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001482	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001631	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0001909	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0002063	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0002133	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0002202	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0002665	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0003510	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0003552	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2526	Microcephaly-lymphedema-chorioretinopathy syndrome		HP:0004936	ORPHA:2526	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000135	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000160	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000218	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000248	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000252	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000278	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000286	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000482	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000518	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000568	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0000582	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0001510	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0002191	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0004322	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2528	Microcephaly-microcornea syndrome, Seemanova type		HP:0010864	ORPHA:2528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0003458	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0003557	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0003707	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0001761	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0008954	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0009005	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0009063	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0030089	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0040081	ORPHA:488650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0002312	ORPHA:488650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0003124	ORPHA:488650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0003760	ORPHA:488650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0008962	ORPHA:488650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0000467	ORPHA:488650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0001962	ORPHA:488650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type		HP:0003326	ORPHA:488650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type	NOT	HP:0001284	ORPHA:488650	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:488650	Distal myopathy, Tateyama type	NOT	HP:0002936	ORPHA:488650	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0000175	ORPHA:2521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0000176	ORPHA:2521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0000193	ORPHA:2521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0000252	ORPHA:2521	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0000278	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0000303	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0000347	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0001249	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0001263	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0001328	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0007703	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2521	Microcephaly-cleft palate-abnormal retinal pigmentation syndrome		HP:0100490	ORPHA:2521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000047	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000069	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000252	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000340	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000347	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000369	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000444	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000470	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000508	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000520	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000767	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000772	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0000889	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0001256	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0001347	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0002167	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0002176	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0002808	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0002949	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0003272	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0003307	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0004312	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0004322	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0006482	ORPHA:2522	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0010620	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2522	Microcephaly-cervical spine fusion anomalies syndrome		HP:0012371	ORPHA:2522	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2523	Microcephaly-brain defect-spasticity-hypernatremia syndrome		HP:0000252	ORPHA:2523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2523	Microcephaly-brain defect-spasticity-hypernatremia syndrome		HP:0001257	ORPHA:2523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2523	Microcephaly-brain defect-spasticity-hypernatremia syndrome		HP:0001360	ORPHA:2523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2523	Microcephaly-brain defect-spasticity-hypernatremia syndrome		HP:0001939	ORPHA:2523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2523	Microcephaly-brain defect-spasticity-hypernatremia syndrome		HP:0002120	ORPHA:2523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2523	Microcephaly-brain defect-spasticity-hypernatremia syndrome		HP:0100543	ORPHA:2523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0001324	ORPHA:401953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0001350	ORPHA:401953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0002172	ORPHA:401953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0000639	ORPHA:401953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0001260	ORPHA:401953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0001337	ORPHA:401953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0002066	ORPHA:401953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0012547	ORPHA:401953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0002076	ORPHA:401953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:401953	Episodic ataxia with slurred speech		HP:0002411	ORPHA:401953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000028	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000218	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000252	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000407	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000482	ORPHA:139471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000518	ORPHA:139471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000528	ORPHA:139471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000545	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000556	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000567	ORPHA:139471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000568	ORPHA:139471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000612	ORPHA:139471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000639	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000647	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0000864	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0001250	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0001263	ORPHA:139471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0001274	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0001830	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0002164	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0006101	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0007068	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139471	Microphthalmia with brain and digit anomalies		HP:0009623	ORPHA:139471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0001260	ORPHA:458803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0001317	ORPHA:458803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002317	ORPHA:458803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0012759	ORPHA:458803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000012	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000716	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0001152	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0001272	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002015	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002064	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002066	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0003487	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0006855	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0006938	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0007979	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0031166	ORPHA:458803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000020	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000486	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000571	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000639	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000651	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0000802	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002321	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002322	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002346	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002511	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0002650	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0003765	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0007351	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0007366	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0012708	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:458803	Spinocerebellar ataxia type 42		HP:0030890	ORPHA:458803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001249	ORPHA:500150	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001263	ORPHA:500150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001999	ORPHA:500150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0012443	ORPHA:500150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000119	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000486	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000540	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000729	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001382	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001511	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001531	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002079	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002119	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002197	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002538	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0003508	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0008872	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0008947	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0010864	ORPHA:500150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000085	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000122	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000175	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000193	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000233	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000286	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000293	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000319	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000322	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000324	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000327	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000341	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000365	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000369	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000411	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000431	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000490	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000494	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000529	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000545	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000565	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000577	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000592	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000609	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000639	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000648	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000891	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0000902	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001027	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001166	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001257	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001627	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0001631	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002007	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002015	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002020	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002028	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002097	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002121	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002126	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002140	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002212	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002283	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002308	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002326	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002376	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002500	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002578	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002579	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002714	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002719	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002751	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002878	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002937	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0002938	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0003100	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0003196	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0004315	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0004433	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0004442	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0004482	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0005280	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0005639	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0006956	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0006970	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0006989	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0007100	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0007933	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0008765	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0009777	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0009879	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0010485	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0011220	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0011330	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0011467	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0011471	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0011648	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0011819	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0012582	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0025116	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0030707	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0045075	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0100307	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0100702	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0100704	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		HP:0430021	ORPHA:500150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0000252	ORPHA:139474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0000682	ORPHA:139474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0001249	ORPHA:139474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0001263	ORPHA:139474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0004322	ORPHA:139474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0006297	ORPHA:139474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0000053	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0000233	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0000272	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0000653	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0000750	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0001250	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0004411	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0009928	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0011803	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139474	17q11.2 microduplication syndrome		HP:0045075	ORPHA:139474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0000252	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0000347	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0001010	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0001263	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0007730	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0009882	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0010185	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2513	Microcephaly-albinism-digital anomalies syndrome		HP:0001263	ORPHA:2513	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2514	Autosomal dominant primary microcephaly		HP:0000252	ORPHA:2514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2514	Autosomal dominant primary microcephaly		HP:0000411	ORPHA:2514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2514	Autosomal dominant primary microcephaly		HP:0000666	ORPHA:2514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2514	Autosomal dominant primary microcephaly		HP:0001137	ORPHA:2514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2514	Autosomal dominant primary microcephaly		HP:0004322	ORPHA:2514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2514	Autosomal dominant primary microcephaly		HP:0009804	ORPHA:2514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0000252	ORPHA:2515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0001249	ORPHA:2515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0001644	ORPHA:2515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0100543	ORPHA:2515	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0000356	ORPHA:2515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0001852	ORPHA:2515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0004209	ORPHA:2515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0004322	ORPHA:2515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0000340	ORPHA:2515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0001250	ORPHA:2515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0001511	ORPHA:2515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0001629	ORPHA:2515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0002119	ORPHA:2515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0002705	ORPHA:2515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2515	Microcephaly-cardiomyopathy syndrome		HP:0007703	ORPHA:2515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000252	ORPHA:2516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0001511	ORPHA:2516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0001629	ORPHA:2516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0002101	ORPHA:2516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0100543	ORPHA:2516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000104	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000175	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000347	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000383	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000430	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000465	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000470	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0000581	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0001252	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0001387	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0001660	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0001679	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0002705	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0004467	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0006610	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0007598	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0008678	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2516	Microcephaly-cardiac defect-lung malsegmentation syndrome		HP:0009882	ORPHA:2516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001249	ORPHA:500159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001263	ORPHA:500159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000252	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000708	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000733	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001250	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001270	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001344	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001627	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002465	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0008872	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0008947	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0011968	ORPHA:500159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000028	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000047	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000194	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000256	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000363	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000403	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000407	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000426	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000463	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000819	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0000964	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001321	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001357	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001382	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001537	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001629	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001643	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001647	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001655	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0001999	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002079	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002119	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002126	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002280	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002365	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002518	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002553	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002650	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0002786	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0003086	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0006532	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0007033	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0008527	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0009237	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0009765	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0030515	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom		HP:0200007	ORPHA:500159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000252	ORPHA:2518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000307	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000340	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000411	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000431	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000463	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000486	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000499	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000505	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000639	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0000648	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0001249	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0001250	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0001276	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0001511	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0002120	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0002269	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0002650	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0004322	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0004422	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0007360	ORPHA:2518	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2518	Autosomal recessive chorioretinopathy-microcephaly syndrome		HP:0007703	ORPHA:2518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000054	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000851	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0001249	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0001250	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0001263	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0001631	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0006934	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0008947	ORPHA:2519	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000028	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000252	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000286	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000565	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000766	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000772	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000773	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0000885	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0001162	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0001629	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0001643	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0002079	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0002092	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0002098	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0002558	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2519	Microcephaly-seizures-intellectual disability-heart disease syndrome		HP:0005989	ORPHA:2519	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000028	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000060	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000064	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000126	ORPHA:2510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000218	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000252	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000322	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000347	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000358	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000400	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000431	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000463	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000480	ORPHA:2510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000482	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000518	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000568	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000648	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000649	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0000823	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001250	ORPHA:2510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001252	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001257	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001263	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001302	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001317	ORPHA:2510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001320	ORPHA:2510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001339	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001387	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0001511	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0002120	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0002230	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0002650	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0002808	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0003196	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0004322	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0007370	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0007703	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0008736	ORPHA:2510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0009830	ORPHA:2510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0010864	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0100542	ORPHA:2510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2510	Micro syndrome		HP:0100704	ORPHA:2510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000239	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000248	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000252	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000270	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000272	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000275	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000276	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000303	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000364	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000446	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000486	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000508	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000598	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000601	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0000767	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0001156	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0001167	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0001172	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0001249	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0001263	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0001328	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0002650	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0003019	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0003172	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0003510	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0004279	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0005469	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0005916	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0007598	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0008818	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0009721	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0009891	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0010668	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0100333	ORPHA:2511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0003307	ORPHA:2511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2511	Microbrachycephaly-ptosis-cleft lip syndrome		HP:0010579	ORPHA:2511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0004322	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0011020	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0012758	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000278	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000286	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000405	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000407	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000431	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000677	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000691	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0002300	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0002650	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0002750	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0002901	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0002942	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0003090	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0003307	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0005280	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0006297	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0006989	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0007042	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0009237	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0009928	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0010663	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0010761	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0030084	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0100255	ORPHA:557003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000121	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000164	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000280	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000365	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000501	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000519	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0000599	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0001297	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0001328	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0001999	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:557003	Oculoskeletodental syndrome		HP:0003072	ORPHA:557003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0000219	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0000252	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0000340	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0000582	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0001263	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0001510	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0002282	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0004322	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0010864	ORPHA:2512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0000076	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0000122	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0001274	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0001302	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0001347	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0002119	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0003103	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2512	Autosomal recessive primary microcephaly		HP:0007333	ORPHA:2512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0001256	ORPHA:500166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0001999	ORPHA:500166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0410263	ORPHA:500166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0000365	ORPHA:500166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0000729	ORPHA:500166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0000924	ORPHA:500166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0001382	ORPHA:500166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0002119	ORPHA:500166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0032059	ORPHA:500166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0040195	ORPHA:500166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0000164	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0000722	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0000736	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0001250	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0001808	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0002213	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0002500	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0002750	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0006989	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500166	SIN3-related intellectual disability syndrome due to a point mutation		HP:0030084	ORPHA:500166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0000280	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0000325	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0000414	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0000448	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0000581	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0001249	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0008947	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293707	Blepharophimosis-intellectual disability syndrome, MKB type		HP:0009928	ORPHA:293707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0002480	ORPHA:529808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0003265	ORPHA:529808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0006579	ORPHA:529808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0006958	ORPHA:529808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0000407	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0000502	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0001249	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0001250	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0001276	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0001343	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0001878	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0001945	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0002871	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0003073	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0011968	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0012696	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0032106	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0100021	ORPHA:529808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0003228	ORPHA:529808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0025518	ORPHA:529808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529808	Chronic bilirubin encephalopathy		HP:0040187	ORPHA:529808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0000405	ORPHA:2502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0001256	ORPHA:2502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0100255	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0000403	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0001169	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0001382	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0001769	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0001773	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0001964	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0002868	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0002970	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0002979	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0003015	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0003016	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0003026	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0003085	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0004279	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0006009	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0006413	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0006417	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0008110	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0008873	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0009760	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0100864	ORPHA:2502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0000486	ORPHA:2502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2502	Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome		HP:0000540	ORPHA:2502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0000104	ORPHA:139466	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0001510	ORPHA:139466	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0001562	ORPHA:139466	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0002089	ORPHA:139466	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0012245	ORPHA:139466	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0000036	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0000047	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0000202	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0000776	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0000834	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0001629	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0001642	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0004794	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0005343	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139466	SERKAL syndrome		HP:0030680	ORPHA:139466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000023	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000028	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000045	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000046	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000047	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000175	ORPHA:2505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000252	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000271	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000286	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000343	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000347	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000358	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000482	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000488	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000568	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000969	ORPHA:2505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0001072	ORPHA:2505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0001249	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0001263	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0001537	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0001635	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0002230	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0003011	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0004322	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0006768	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0007400	ORPHA:2505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0007522	ORPHA:2505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0000377	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0100559	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2505	Multiple benign circumferential skin creases on limbs		HP:0100560	ORPHA:2505	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95626	Acquired arginine vasopressin deficiency		HP:0000873	ORPHA:95626	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95626	Acquired arginine vasopressin deficiency		HP:0001824	ORPHA:95626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95626	Acquired arginine vasopressin deficiency		HP:0001959	ORPHA:95626	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95626	Acquired arginine vasopressin deficiency		HP:0100515	ORPHA:95626	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000023	ORPHA:2508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000047	ORPHA:2508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000110	ORPHA:2508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000252	ORPHA:2508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000280	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000411	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000486	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0000639	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0001250	ORPHA:2508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0001257	ORPHA:2508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0001274	ORPHA:2508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0002120	ORPHA:2508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0002230	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0002445	ORPHA:2508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0002650	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0003272	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0004322	ORPHA:2508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0008678	ORPHA:2508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0010720	ORPHA:2508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0010864	ORPHA:2508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2508	Corpus callosum agenesis-abnormal genitalia syndrome		HP:0011344	ORPHA:2508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0005987	ORPHA:276399	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0002671	ORPHA:276399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0005584	ORPHA:276399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0100528	ORPHA:276399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0100615	ORPHA:276399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0100617	ORPHA:276399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0100619	ORPHA:276399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0200063	ORPHA:276399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0002890	ORPHA:276399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0006779	ORPHA:276399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0007129	ORPHA:276399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0030071	ORPHA:276399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter		HP:0030434	ORPHA:276399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276399	Familial multinodular goiter	NOT	HP:0000836	ORPHA:276399	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0000347	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0000444	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0000951	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0000963	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0001249	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0001773	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0002213	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0002650	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0002652	ORPHA:2500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0004322	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0001382	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0007392	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0007400	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0007495	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0008065	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0100578	ORPHA:2500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0100585	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0200042	ORPHA:2500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2500	Acrogeria		HP:0200055	ORPHA:2500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0000164	ORPHA:2501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0000670	ORPHA:2501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0000944	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0001288	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0001385	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0002650	ORPHA:2501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0002750	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0002970	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0003307	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0003498	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0004349	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0005871	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0005930	ORPHA:2501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0006385	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0006409	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0006487	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2501	Metaphyseal chondrodysplasia, Spahr type		HP:0100255	ORPHA:2501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0011923	ORPHA:2609	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000114	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000407	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000486	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000508	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000543	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000639	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000817	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001138	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001251	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001252	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001254	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001263	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001298	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001324	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001508	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001511	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001639	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0001943	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0002013	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0002093	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0002240	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0002352	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0002415	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0002421	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0002490	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0003128	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0003542	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0003737	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0007704	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0008316	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0012748	ORPHA:2609	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000252	ORPHA:2609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000618	ORPHA:2609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0000819	ORPHA:2609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0011968	ORPHA:2609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2609	Isolated complex I deficiency		HP:0025116	ORPHA:2609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0000952	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001399	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001518	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001622	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001744	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0002027	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0002240	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0002910	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0003077	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0003155	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0004359	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0006560	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0011113	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0011473	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0030948	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0032245	ORPHA:567983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001081	ORPHA:567983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001394	ORPHA:567983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001395	ORPHA:567983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001397	ORPHA:567983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0001409	ORPHA:567983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567983	Parenteral nutrition-associated cholestasis		HP:0002908	ORPHA:567983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000269	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000324	ORPHA:2612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000478	ORPHA:2612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000504	ORPHA:2612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000506	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000568	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000612	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0000995	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001048	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001249	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001250	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001252	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001305	ORPHA:2612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001315	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001347	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001357	ORPHA:2612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001510	ORPHA:2612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0001596	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0002007	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0002119	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0002132	ORPHA:2612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0002353	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0002514	ORPHA:2612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0002816	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0003422	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0004422	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0007360	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0007370	ORPHA:2612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0007400	ORPHA:2612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0009720	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2612	Linear nevus sebaceus syndrome		HP:0100555	ORPHA:2612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2613	Nail-patella-like renal disease		HP:0000083	ORPHA:2613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2613	Nail-patella-like renal disease		HP:0000093	ORPHA:2613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2613	Nail-patella-like renal disease		HP:0000822	ORPHA:2613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2613	Nail-patella-like renal disease		HP:0002907	ORPHA:2613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2613	Nail-patella-like renal disease		HP:0004322	ORPHA:2613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2613	Nail-patella-like renal disease		HP:0100820	ORPHA:2613	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0025186	ORPHA:91412	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0000486	ORPHA:91412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0000646	ORPHA:91412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0007687	ORPHA:91412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0010824	ORPHA:91412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0025584	ORPHA:91412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0008897	ORPHA:91412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0012758	ORPHA:91412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0012803	ORPHA:91412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0020041	ORPHA:91412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0031747	ORPHA:91412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0000078	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0000175	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0000453	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0000589	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0000787	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0001627	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0004408	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0025514	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0031703	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91412	Marcus-Gunn syndrome		HP:0410030	ORPHA:91412	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001597	ORPHA:2614	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0011297	ORPHA:2614	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000077	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001369	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001371	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001763	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002019	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002815	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002987	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003199	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003418	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0008034	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0008110	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0009780	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0009811	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0012718	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0100798	ORPHA:2614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000083	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000093	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000100	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000123	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000348	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000478	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000767	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000790	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0000939	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001250	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001377	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001762	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001771	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001772	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0001884	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002650	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002823	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002938	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002967	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002992	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002999	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003045	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003065	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003083	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003302	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003304	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0003774	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0004209	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0004349	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0004722	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0005190	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0006297	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0006380	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0006394	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0006443	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0007328	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0007906	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0008007	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0008124	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0009697	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0009760	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0009781	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0009890	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0010829	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0010886	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0012108	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0030051	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0030839	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0031006	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0031910	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0045086	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0100797	ORPHA:2614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0002597	ORPHA:2614	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0005290	ORPHA:2614	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2614	Nail-patella syndrome		HP:0006702	ORPHA:2614	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91414	Pilomatrixoma		HP:0030434	ORPHA:91414	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:91414	Pilomatrixoma		HP:0001482	ORPHA:91414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91414	Pilomatrixoma		HP:0012288	ORPHA:91414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91414	Pilomatrixoma		HP:0010766	ORPHA:91414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91414	Pilomatrixoma		HP:0000989	ORPHA:91414	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91414	Pilomatrixoma		HP:0033559	ORPHA:91414	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000047	ORPHA:2616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000144	ORPHA:2616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000232	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000268	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000307	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000325	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000337	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000343	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000411	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000414	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000463	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000470	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000574	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000682	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000684	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000883	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000888	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0000944	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0001374	ORPHA:2616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0001511	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0001838	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0002007	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0002650	ORPHA:2616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0002750	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0002808	ORPHA:2616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0002983	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0003022	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0003100	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0003173	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0003175	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0003307	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0003691	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0004209	ORPHA:2616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0004322	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0004570	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0001382	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0008839	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0009811	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0010306	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0011800	ORPHA:2616	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0100625	ORPHA:2616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2616	3M syndrome		HP:0100659	ORPHA:2616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000028	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000174	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000252	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000347	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000358	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000444	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000508	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000670	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000958	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0000975	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0001249	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0001276	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0001347	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0002162	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0002216	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0002293	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0002353	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0002650	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0002808	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0003422	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0003510	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0004349	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0004399	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0006610	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0007477	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0007495	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0009721	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0010807	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0011362	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2617	Microcephalic primordial dwarfism, Montreal type		HP:0100578	ORPHA:2617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0000522	ORPHA:91416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0000491	ORPHA:91416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0000508	ORPHA:91416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0000509	ORPHA:91416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0000613	ORPHA:91416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0007732	ORPHA:91416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0009743	ORPHA:91416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0200020	ORPHA:91416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima		HP:0007820	ORPHA:91416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91416	Isolated congenital alacrima	NOT	HP:0002571	ORPHA:91416	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0000926	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0000938	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0001831	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0002654	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0002829	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0003028	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0003368	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0003510	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0005086	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0005872	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0008843	ORPHA:2619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0001376	ORPHA:2619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0003019	ORPHA:2619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0003940	ORPHA:2619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0009742	ORPHA:2619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0032153	ORPHA:2619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type		HP:0003179	ORPHA:2619	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type	NOT	HP:0002960	ORPHA:2619	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2619	Brachydactylous dwarfism, Mseleni type	NOT	HP:0012649	ORPHA:2619	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0001289	ORPHA:33543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0007200	ORPHA:33543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0100543	ORPHA:33543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000613	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000713	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000716	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000737	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000739	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000741	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000975	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0001945	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0002167	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0002315	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0002591	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0007057	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0008762	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0010534	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0012658	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:5200321	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0031249	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0034004	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0100738	ORPHA:33543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000622	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0000746	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0001350	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0001959	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0002018	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0002300	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0002519	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0004396	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0025233	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0030221	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0031217	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:0046504	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33543	Kleine-Levin syndrome		HP:5200218	ORPHA:33543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000077	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000256	ORPHA:2611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000481	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000486	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000518	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000612	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000929	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000962	ORPHA:2611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0001250	ORPHA:2611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0001268	ORPHA:2611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0001305	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0001770	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0001883	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0002119	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0002650	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0002652	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0002816	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0004349	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0007370	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0008060	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0009592	ORPHA:2611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0010049	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0100006	ORPHA:2611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0000488	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0002148	ORPHA:2611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0002209	ORPHA:2611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2611	Linear verrucous nevus syndrome		HP:0012500	ORPHA:2611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0002359	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0002505	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003202	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003236	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003325	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003391	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003458	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003551	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003749	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0040287	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0001263	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0001284	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0001488	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0001611	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0001771	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0002015	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0002194	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0003324	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0008981	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0009073	ORPHA:254361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0001270	ORPHA:254361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0009053	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0025435	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0040266	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0430025	ORPHA:254361	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0001626	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0002086	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0002206	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0002875	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0004631	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0011712	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0011950	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17		HP:0100750	ORPHA:254361	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17	NOT	HP:0000951	ORPHA:254361	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:254361	Plectin-related limb-girdle muscular dystrophy R17	NOT	HP:0030208	ORPHA:254361	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000581	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0001181	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0001250	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0002521	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0008947	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0010864	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0011343	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0011451	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0100587	ORPHA:293725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000185	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000278	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000293	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000311	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000319	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000322	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000358	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000391	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000395	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000414	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000437	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000448	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0000807	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0001562	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0002190	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0002339	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0005274	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0006191	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0006956	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0006970	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0009928	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0010761	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293725	Blepharophimosis-intellectual disability syndrome, Verloes type		HP:0011251	ORPHA:293725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623789	Body integrity dysphoria		HP:0000712	ORPHA:623789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623789	Body integrity dysphoria		HP:0003690	ORPHA:623789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623789	Body integrity dysphoria		HP:0008441	ORPHA:623789	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:623789	Body integrity dysphoria		HP:0000739	ORPHA:623789	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:623789	Body integrity dysphoria		HP:0100738	ORPHA:623789	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:623789	Body integrity dysphoria		HP:0100753	ORPHA:623789	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0001369	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0001387	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0001288	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0002829	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0005187	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0005194	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0010219	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0010630	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0010741	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0025238	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0040034	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0040188	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0100039	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0100662	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0100925	ORPHA:564003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0010672	ORPHA:564003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0010885	ORPHA:564003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0008089	ORPHA:564003	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:564003	Osteochondrosis of the metatarsal bone		HP:0040035	ORPHA:564003	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000021	ORPHA:2604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000072	ORPHA:2604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000076	ORPHA:2604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0003270	ORPHA:2604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0010318	ORPHA:2604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000175	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000252	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000311	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000337	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000347	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000358	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000426	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000463	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000774	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0000843	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0001166	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0001387	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0001537	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0001798	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0002251	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0003363	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0030680	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2604	Familial visceral myopathy		HP:0100490	ORPHA:2604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0000028	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0000047	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0000485	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0000492	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0000505	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0001249	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0001257	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0001263	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0005517	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0008619	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2608	N syndrome		HP:0012372	ORPHA:2608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0000252	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0000717	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0000718	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0001249	ORPHA:254351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0001250	ORPHA:254351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0001328	ORPHA:254351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0001631	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0001643	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0002132	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0002308	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0007018	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254351	Distal 7q11.23 microdeletion syndrome		HP:0007302	ORPHA:254351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0001249	ORPHA:313892	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0001270	ORPHA:313892	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000750	ORPHA:313892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0430028	ORPHA:313892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000189	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000486	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000545	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000577	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000648	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000678	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000739	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000768	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0001252	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0002007	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0002711	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0002938	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0002948	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0004691	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0005659	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0012443	ORPHA:313892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000078	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000718	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0000733	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0001250	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0001653	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0002020	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0002650	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0003316	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0007018	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0011968	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313892	Developmental and speech delay due to SOX5 deficiency		HP:0100716	ORPHA:313892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0002979	ORPHA:156728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0004322	ORPHA:156728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0009826	ORPHA:156728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0001377	ORPHA:156728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0002515	ORPHA:156728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0002938	ORPHA:156728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0008873	ORPHA:156728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0000767	ORPHA:156728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0003037	ORPHA:156728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0005257	ORPHA:156728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:156728	Spondyloepimetaphyseal dysplasia, matrilin-3 type		HP:0012368	ORPHA:156728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0010831	ORPHA:319199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0002169	ORPHA:319199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0007350	ORPHA:319199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0000750	ORPHA:319199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0000768	ORPHA:319199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0002808	ORPHA:319199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0001382	ORPHA:319199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0200049	ORPHA:319199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0000365	ORPHA:319199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0002451	ORPHA:319199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0002495	ORPHA:319199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0000252	ORPHA:319199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0000372	ORPHA:319199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0001508	ORPHA:319199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0002119	ORPHA:319199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319199	Autosomal recessive spastic paraplegia type 53		HP:0002539	ORPHA:319199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0000704	ORPHA:75392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0001034	ORPHA:75392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0001075	ORPHA:75392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0004322	ORPHA:75392	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0000212	ORPHA:75392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0000691	ORPHA:75392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0000974	ORPHA:75392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0001382	ORPHA:75392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0006308	ORPHA:75392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0006349	ORPHA:75392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0000347	ORPHA:75392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75392	Periodontal Ehlers-Danlos syndrome		HP:0006323	ORPHA:75392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0000347	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0000388	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0000926	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0002750	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0000938	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0000939	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0100255	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0000975	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0001288	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0009926	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0004322	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0001595	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0001812	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0001288	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0002656	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0002815	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0003025	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0003045	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0003084	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0003886	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0006482	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0007642	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0008110	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0008124	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0008404	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0008394	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0012542	ORPHA:319195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319195	Chondroectodermal dysplasia with night blindness		HP:0030055	ORPHA:319195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0002126	ORPHA:300573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0002539	ORPHA:300573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0100543	ORPHA:300573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0000252	ORPHA:300573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001249	ORPHA:300573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001263	ORPHA:300573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001269	ORPHA:300573	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0000486	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001250	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001272	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001273	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001302	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0002079	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0002282	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0002339	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0002363	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0002389	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0006956	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0007018	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0007301	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0007359	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0008947	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0012110	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0012377	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0012650	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0025102	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0025160	ORPHA:300573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001274	ORPHA:300573	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0001339	ORPHA:300573	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300573	Polymicrogyria due to TUBB2B mutation		HP:0010636	ORPHA:300573	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0000764	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002143	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002936	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0004359	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0007199	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0009053	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0030177	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0031064	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0040078	ORPHA:139399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0000849	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0001000	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0001257	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0001347	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002064	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002213	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002607	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002839	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0003487	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0006827	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0007006	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0007266	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0007372	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0008167	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0008969	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0009830	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0010284	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0011749	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0012378	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0030014	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0031845	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0040307	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0100291	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0100639	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0100816	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0410263	ORPHA:139399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0000012	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0000016	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0000020	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0000708	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0000846	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0001260	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002292	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0002354	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0003418	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0004302	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0008207	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0012534	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0100502	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139399	Adrenomyeloneuropathy		HP:0100543	ORPHA:139399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0003089	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0007034	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0007663	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0010527	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0010794	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0011448	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0030222	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0031993	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0040288	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0045084	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000618	ORPHA:139396	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002540	ORPHA:139396	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0031358	ORPHA:139396	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002518	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0003477	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0004302	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0004359	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0007141	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0012501	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000026	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000317	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000365	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000657	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000736	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000752	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001250	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001251	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001260	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001269	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001285	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001288	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001289	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001310	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002015	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002061	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002167	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002186	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002354	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001288	ORPHA:139396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001268	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002196	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0007162	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0007305	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0008163	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0008167	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0008207	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0009830	ORPHA:139396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0000708	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0001328	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002143	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:139396	X-linked cerebral adrenoleukodystrophy		HP:0002283	ORPHA:139396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001250	ORPHA:300570	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001263	ORPHA:300570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000486	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000496	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000565	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000639	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001249	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001257	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001321	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001338	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001339	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001488	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002079	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002126	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002194	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002334	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002365	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002465	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002474	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002497	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002540	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0007260	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0008872	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0008897	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0008936	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0009879	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0010862	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0011344	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0025336	ORPHA:300570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000218	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000256	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000286	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000347	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000369	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000407	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000473	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000494	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000570	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000572	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000609	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000657	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000712	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000733	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0012760	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0000736	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001260	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001264	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001320	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001332	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001357	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001382	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001491	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001773	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0001840	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002134	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002343	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002510	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002751	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002857	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002943	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0002967	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0005216	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0005469	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0006956	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0007048	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0007359	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0008619	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0010663	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0011451	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0012332	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0012434	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0012697	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0025101	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0030302	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0030534	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0030903	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0040326	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0100785	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation		HP:0200055	ORPHA:300570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000059	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000160	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000293	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000358	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000407	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000486	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000494	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000527	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000556	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000574	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000637	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000648	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000687	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000691	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0001182	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0001488	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0001511	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0001602	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0001686	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0001799	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0001822	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0003186	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0008757	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0009183	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0009537	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0009600	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0010066	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0010193	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0010864	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0011304	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0011968	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0012471	ORPHA:324540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000048	ORPHA:324540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000064	ORPHA:324540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324540	Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome		HP:0000046	ORPHA:324540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0000089	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0000232	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0000343	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0000377	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0000463	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0000582	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0001162	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0001252	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0001321	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0001511	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0001596	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0001629	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0001631	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0002208	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0002299	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0004322	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0004415	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0005280	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0006610	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0006817	ORPHA:75389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0008404	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0011344	ORPHA:75389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0011747	ORPHA:75389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75389	Brain malformation-congenital heart disease-postaxial polydactyly syndrome		HP:0011757	ORPHA:75389	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000369	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000411	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000750	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001249	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001263	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001290	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001999	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0002079	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0002194	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0006863	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0008468	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0008472	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0008897	ORPHA:480907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000218	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000276	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000307	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000336	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000343	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000365	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000389	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000463	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000486	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000494	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000729	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001382	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0002342	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0200136	ORPHA:480907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000219	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000252	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000286	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000347	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000414	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000455	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000490	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000527	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000574	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0000664	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001250	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001264	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001332	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001337	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0001513	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0002395	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0005280	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480907	X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome		HP:0012032	ORPHA:480907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0000648	ORPHA:254343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0001260	ORPHA:254343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0001347	ORPHA:254343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0002313	ORPHA:254343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0003487	ORPHA:254343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0000182	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0000639	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0001270	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0001336	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0002073	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0002359	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0006895	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0007240	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0200049	ORPHA:254343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0000712	ORPHA:254343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254343	Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome		HP:0001265	ORPHA:254343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000028	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000047	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000175	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000233	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000248	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000252	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000286	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000316	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000337	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000343	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000369	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000405	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000407	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000446	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000463	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000470	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000486	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000520	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000545	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000639	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000664	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000668	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000750	ORPHA:254346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000752	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000821	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000826	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001250	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001252	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001263	ORPHA:254346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001363	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001397	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001511	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001513	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001629	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001631	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001653	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001659	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001852	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001863	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0001869	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0002079	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0002119	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0002230	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0002650	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0002804	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0002808	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0003077	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0004209	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0004279	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0006101	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0006191	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0006817	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0000377	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0011675	ORPHA:254346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254346	19p13.12 microdeletion syndrome		HP:0100716	ORPHA:254346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0001638	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0001663	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0001714	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0001962	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0002321	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0002875	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0003199	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0003458	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0003484	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0003547	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0003722	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0004756	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0005144	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0009023	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0009027	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0010872	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0011675	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0011712	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0012251	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0012270	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0031319	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency		HP:0040014	ORPHA:263297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency	NOT	HP:0000819	ORPHA:263297	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency	NOT	HP:0000821	ORPHA:263297	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:263297	Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency	NOT	HP:0040081	ORPHA:263297	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000750	ORPHA:319182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000219	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000311	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000316	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000324	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000343	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000431	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000527	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000574	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000708	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000718	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000733	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000736	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000739	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000744	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000752	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000824	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001182	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001252	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0002015	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0002194	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0002750	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0004540	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0005616	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0008897	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0009811	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0011968	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0012745	ORPHA:319182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000218	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000252	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000268	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000286	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000348	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000369	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000465	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000506	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000508	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000664	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000767	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0000960	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001155	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001249	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001250	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001273	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001508	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0001511	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0002020	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0002230	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0002361	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0003196	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0004209	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0004322	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0006712	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0008905	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0010485	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0012368	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0030084	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319182	Wiedemann-Steiner syndrome		HP:0100581	ORPHA:319182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0000969	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0001482	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0001744	ORPHA:33577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0001824	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0001945	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0002017	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0002027	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0002240	ORPHA:33577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0002829	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0002960	ORPHA:33577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0003326	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0008065	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0010783	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0012490	ORPHA:33577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33577	Nodular non-suppurative panniculitis		HP:0100533	ORPHA:33577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0025289	ORPHA:50918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0000155	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0000988	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0000989	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0000992	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001596	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001824	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001882	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002039	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002633	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002716	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002733	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0010783	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0011134	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0012378	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0025143	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0025300	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0025435	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0030166	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0100540	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0200029	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0200036	ORPHA:50918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0000464	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001287	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001744	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001873	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001875	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001903	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002829	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002910	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0003326	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0003493	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0003565	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0006530	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0008066	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0011024	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0011227	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0011801	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0012733	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0025475	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0100827	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0200034	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0200035	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0200041	ORPHA:50918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0001251	ORPHA:50918	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002202	ORPHA:50918	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0002240	ORPHA:50918	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0008940	ORPHA:50918	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0012819	ORPHA:50918	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50918	Kikuchi-Fujimoto disease		HP:0200039	ORPHA:50918	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000023	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000098	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000160	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000218	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000316	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000348	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000369	ORPHA:217385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000445	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000470	ORPHA:217385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0000494	ORPHA:217385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0001252	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0001263	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0001374	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0002007	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0002079	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0002119	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0003196	ORPHA:217385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0004209	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217385	17p13.3 microduplication syndrome		HP:0008736	ORPHA:217385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0003477	ORPHA:497764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0008959	ORPHA:497764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0009053	ORPHA:497764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0000571	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0000768	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0001260	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0001265	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0001284	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0001761	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0002066	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0002070	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0002317	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0002396	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0002936	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0003387	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0003693	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0007141	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0009027	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0012531	ORPHA:497764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0002073	ORPHA:497764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43		HP:0006855	ORPHA:497764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:497764	Spinocerebellar ataxia type 43	NOT	HP:0000726	ORPHA:497764	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0000969	ORPHA:449285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0010783	ORPHA:449285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0011355	ORPHA:449285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0012531	ORPHA:449285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0031364	ORPHA:449285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0000707	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0001297	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0001649	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0001873	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0001892	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0001928	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002013	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002170	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002637	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0003201	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0003470	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0003713	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0007024	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0009088	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0011900	ORPHA:449285	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0000225	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0000421	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0001658	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0001919	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002014	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002068	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002203	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002615	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002878	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0002902	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0005521	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0030149	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0040075	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449285	Snakebite envenomation		HP:0100665	ORPHA:449285	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001250	ORPHA:529665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0002353	ORPHA:529665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000316	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000341	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000455	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000463	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000545	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000639	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000657	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000750	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000938	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000939	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001256	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001257	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001260	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001272	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001290	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001310	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001321	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001337	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001347	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0002066	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0002069	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0001288	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0003698	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0011220	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0012758	ORPHA:529665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000505	ORPHA:529665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0000648	ORPHA:529665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome		HP:0002133	ORPHA:529665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome	NOT	HP:0003155	ORPHA:529665	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000750	ORPHA:391372	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002474	ORPHA:391372	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0009088	ORPHA:391372	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0011220	ORPHA:391372	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000119	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000194	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000303	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000316	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000403	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000455	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000478	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000486	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000494	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000508	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000539	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000708	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000729	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000736	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000739	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000954	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001257	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001270	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001371	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001508	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001627	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002019	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002236	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002342	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002714	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002788	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0003196	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0005272	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0007301	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0008762	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0010864	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0011823	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0011968	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0012471	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0410263	ORPHA:391372	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000077	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000256	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000278	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000581	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000598	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000639	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000819	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0000821	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001212	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001250	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001252	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001256	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0001581	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002092	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0002353	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0007018	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0008589	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0012393	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0025502	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0030084	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391372	FOXP1 Syndrome		HP:0040303	ORPHA:391372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0001945	ORPHA:449280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002721	ORPHA:449280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0032169	ORPHA:449280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0032255	ORPHA:449280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0001482	ORPHA:449280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002090	ORPHA:449280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0010766	ORPHA:449280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0032162	ORPHA:449280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0032262	ORPHA:449280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0000246	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0000819	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0001701	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0001977	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002102	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002105	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002206	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002754	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002795	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0002878	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0003095	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0005059	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0005265	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0011450	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0011919	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0012210	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0012387	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0012735	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0020101	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0031994	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0032159	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0032176	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0100584	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0100806	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449280	Scedosporiosis		HP:0410263	ORPHA:449280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0001284	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0003474	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0003484	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0007340	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0011964	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0012735	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0030179	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0030200	ORPHA:90117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0000079	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0001337	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0002483	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0002540	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0002936	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0003236	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0003698	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0007289	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0010546	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0030007	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0031910	ORPHA:90117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0002015	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0002094	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0002878	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0004887	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0010827	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0011014	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0011470	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0011951	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90117	Hereditary motor and sensory neuropathy, Okinawa type		HP:0410262	ORPHA:90117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0000717	ORPHA:217377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0000750	ORPHA:217377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0000826	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001249	ORPHA:217377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001250	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001513	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001609	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001611	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001761	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001763	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0001770	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217377	Microduplication Xp11.22p11.23 syndrome		HP:0012557	ORPHA:217377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001878	ORPHA:33574	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0002503	ORPHA:33574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0003198	ORPHA:33574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0003355	ORPHA:33574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0009830	ORPHA:33574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0000709	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0000952	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001249	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001251	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001260	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001263	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001347	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001433	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0001923	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33574	Glutamate-cysteine ligase deficiency		HP:0010522	ORPHA:33574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0000317	ORPHA:324588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0002310	ORPHA:324588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0001260	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0001332	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0001336	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0002072	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0002322	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0001288	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0002509	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0008936	ORPHA:324588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0001347	ORPHA:324588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0001635	ORPHA:324588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0001644	ORPHA:324588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia		HP:0002194	ORPHA:324588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324588	Familial dyskinesia and facial myokymia	NOT	HP:0001249	ORPHA:324588	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0000762	ORPHA:90103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0001256	ORPHA:90103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0003387	ORPHA:90103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0007078	ORPHA:90103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0007141	ORPHA:90103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0007210	ORPHA:90103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0008625	ORPHA:90103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0001260	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0001263	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0001344	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0001531	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0001761	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0002066	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0002522	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0003134	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0003409	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0003438	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0006938	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0008944	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0008954	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0008959	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0008962	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0009027	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0009031	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0009053	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0009129	ORPHA:90103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0002093	ORPHA:90103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0012046	ORPHA:90103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome		HP:0012531	ORPHA:90103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90103	Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome	NOT	HP:0040078	ORPHA:90103	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0000286	ORPHA:324581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0000316	ORPHA:324581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0000341	ORPHA:324581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0001265	ORPHA:324581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0001290	ORPHA:324581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0001072	ORPHA:324581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0001270	ORPHA:324581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0001612	ORPHA:324581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0000160	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0000268	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0000431	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0001254	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0002058	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0002380	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0002795	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0003687	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0011220	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0031139	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324581	Benign Samaritan congenital myopathy		HP:0031237	ORPHA:324581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:25968	Self-limited childhood occipital epilepsy		HP:0002384	ORPHA:25968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:25968	Self-limited childhood occipital epilepsy		HP:0012011	ORPHA:25968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:25968	Self-limited childhood occipital epilepsy		HP:0002013	ORPHA:25968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25968	Self-limited childhood occipital epilepsy		HP:0002315	ORPHA:25968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25968	Self-limited childhood occipital epilepsy		HP:0002367	ORPHA:25968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:25968	Self-limited childhood occipital epilepsy		HP:0025518	ORPHA:25968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0000605	ORPHA:251282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0001276	ORPHA:251282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0001347	ORPHA:251282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002061	ORPHA:251282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0000514	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0001258	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002015	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002064	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002070	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002354	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0001288	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002464	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002497	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0003487	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0006961	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0008969	ORPHA:251282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0000492	ORPHA:251282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0000508	ORPHA:251282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0001332	ORPHA:251282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0001337	ORPHA:251282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0001761	ORPHA:251282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0002166	ORPHA:251282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1		HP:0010831	ORPHA:251282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1	NOT	HP:0001250	ORPHA:251282	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1	NOT	HP:0002921	ORPHA:251282	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:251282	Autosomal dominant spastic ataxia type 1	NOT	HP:0003700	ORPHA:251282	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0000750	ORPHA:208444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0001249	ORPHA:208444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0001263	ORPHA:208444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0001256	ORPHA:208444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0001285	ORPHA:208444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0001250	ORPHA:208444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0001269	ORPHA:208444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0002353	ORPHA:208444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0004302	ORPHA:208444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria		HP:0006801	ORPHA:208444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208444	Bilateral frontal polymicrogyria	NOT	HP:0002200	ORPHA:208444	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000750	ORPHA:208441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0002194	ORPHA:208441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0002539	ORPHA:208441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0010862	ORPHA:208441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000708	ORPHA:208441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0001249	ORPHA:208441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0001250	ORPHA:208441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0001263	ORPHA:208441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0002069	ORPHA:208441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000174	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000252	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000256	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000365	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000486	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000505	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000718	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0000951	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0001252	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0001257	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0001345	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0001999	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0002367	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0002384	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0007024	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0008765	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0011297	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0031258	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0031589	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208441	Bilateral parasagittal parieto-occipital polymicrogyria		HP:0100852	ORPHA:208441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0000825	ORPHA:324575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001319	ORPHA:324575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001998	ORPHA:324575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0030796	ORPHA:324575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0031084	ORPHA:324575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0040299	ORPHA:324575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0000713	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0000842	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0000980	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001069	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001520	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001649	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001962	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001985	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0002173	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0002329	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0003162	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0004904	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0012051	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0012759	ORPHA:324575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001254	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001279	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001325	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0001518	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0002591	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0007185	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0009800	ORPHA:324575	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0011968	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0012734	ORPHA:324575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324575	Hyperinsulinism due to HNF1A deficiency		HP:0002240	ORPHA:324575	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002240	ORPHA:264580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002910	ORPHA:264580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0012379	ORPHA:264580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0030272	ORPHA:264580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001395	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001510	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001943	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001946	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002155	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003124	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003162	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0410175	ORPHA:264580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0000147	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0000823	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0000858	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0000876	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001249	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001263	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001396	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001397	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001508	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002194	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002360	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002719	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002913	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003202	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003236	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003323	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003326	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003394	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003546	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0004322	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0012378	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0030232	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0100607	ORPHA:264580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0000750	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0000939	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001252	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001394	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001638	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001744	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001903	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0001947	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002013	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002014	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002018	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0002040	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0003128	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0004324	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0006580	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264580	Glycogen storage disease due to liver phosphorylase kinase deficiency		HP:0012028	ORPHA:264580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001263	ORPHA:544469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001285	ORPHA:544469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001344	ORPHA:544469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002020	ORPHA:544469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002540	ORPHA:544469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0008936	ORPHA:544469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0010864	ORPHA:544469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0000252	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001250	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001272	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001357	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002059	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002093	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002169	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002353	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002650	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0008872	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0012448	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0032794	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0033725	ORPHA:544469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0000347	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0000369	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0000518	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0000648	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001308	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001347	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001639	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0001776	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0003236	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0011097	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0100704	ORPHA:544469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0000488	ORPHA:544469	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544469	PRUNE1-related neurological syndrome		HP:0002313	ORPHA:544469	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0000822	ORPHA:251274	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0040084	ORPHA:251274	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0002900	ORPHA:251274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0008221	ORPHA:251274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0011740	ORPHA:251274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0000360	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0000421	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0001324	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0001657	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0001712	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0001959	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0002018	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0002150	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0002170	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0002315	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III		HP:0200114	ORPHA:251274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251274	Familial hyperaldosteronism type III	NOT	HP:0011739	ORPHA:251274	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002194	ORPHA:208447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0012736	ORPHA:208447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0031936	ORPHA:208447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0000708	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0000733	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0001257	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002197	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002300	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002510	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0008936	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0010864	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0011968	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0100022	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0100704	ORPHA:208447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0000252	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0000729	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0001256	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0001332	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0001510	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002020	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002069	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002079	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002123	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002133	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002187	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002342	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002360	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0004322	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0005216	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0006956	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0007166	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0007204	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0007359	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0007824	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0010553	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0010818	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0010819	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0010821	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0011147	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0011153	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0011344	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0012469	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0012704	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0025097	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0025100	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0025517	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0040288	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0100660	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0100716	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0200136	ORPHA:208447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:208447	Bilateral generalized polymicrogyria		HP:0002376	ORPHA:208447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0000389	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0001047	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0002090	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0002099	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0002205	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0003212	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0004429	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0005401	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0005403	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0005406	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0010976	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0011108	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0012203	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0200042	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0200043	ORPHA:217390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0002860	ORPHA:217390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0006763	ORPHA:217390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217390	Combined immunodeficiency due to DOCK8 deficiency		HP:0030417	ORPHA:217390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006350	ORPHA:49042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006486	ORPHA:49042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0000683	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0000694	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0001382	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006282	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006286	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006479	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0010299	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0011084	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0025124	ORPHA:49042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0000978	ORPHA:49042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0001592	ORPHA:49042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006094	ORPHA:49042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006335	ORPHA:49042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0006336	ORPHA:49042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0010485	ORPHA:49042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0045086	ORPHA:49042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0000365	ORPHA:49042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0000592	ORPHA:49042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49042	Dentinogenesis imperfecta		HP:0003010	ORPHA:49042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0012531	ORPHA:49041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000083	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000126	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000822	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0001824	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0001897	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0002027	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0002039	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0003138	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0003259	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0003419	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0003565	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0005310	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0011227	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0012378	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0012583	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0025379	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0030157	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0031191	ORPHA:49041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000074	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000872	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0001370	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0001919	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0001945	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0002017	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0002019	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0002725	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0002923	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0003262	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0003453	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0003765	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0010741	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0012578	ORPHA:49041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000034	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000100	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000790	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0000802	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0002639	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0008682	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0012871	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0012877	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0100518	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49041	IgG4-related retroperitoneal fibrosis		HP:0100817	ORPHA:49041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000047	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000252	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000750	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001057	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001249	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001508	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001510	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001511	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0004209	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0004326	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0011968	ORPHA:217346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000028	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000233	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000276	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000278	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000348	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000430	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000958	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000963	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001770	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001863	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0002164	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0002205	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0002213	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0002558	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0005338	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0006101	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0006610	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0008070	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0010761	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0200102	ORPHA:217346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000048	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000154	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000365	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000482	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0000518	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001374	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0001629	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0006315	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217346	19q13.11 microdeletion syndrome		HP:0030680	ORPHA:217346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88643	Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome		HP:0000851	ORPHA:88643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88643	Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome		HP:0001263	ORPHA:88643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88643	Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome		HP:0001363	ORPHA:88643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88643	Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome		HP:0001513	ORPHA:88643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88643	Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome		HP:0001640	ORPHA:88643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88643	Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome		HP:0002583	ORPHA:88643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88643	Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome		HP:0003073	ORPHA:88643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001251	ORPHA:88644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001272	ORPHA:88644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001288	ORPHA:88644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002493	ORPHA:88644	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0000736	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001257	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001270	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001315	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001347	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002061	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002380	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0003202	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0003487	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0007340	ORPHA:88644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0000020	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0000486	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0000508	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0000570	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0000597	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001249	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001260	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001310	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001319	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001558	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001761	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002312	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002500	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002650	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002808	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0003445	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0007267	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0007772	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0011448	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0025402	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0031960	ORPHA:88644	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0001271	ORPHA:88644	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002086	ORPHA:88644	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0002495	ORPHA:88644	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0003390	ORPHA:88644	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0007178	ORPHA:88644	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88644	Autosomal recessive ataxia, Beauce type		HP:0007366	ORPHA:88644	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000164	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000218	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000252	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000272	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000286	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000322	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000347	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000356	ORPHA:217340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000463	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000574	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000664	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000717	ORPHA:217340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000722	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000729	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0000823	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0001249	ORPHA:217340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0001252	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0001263	ORPHA:217340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0001508	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0001770	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0001852	ORPHA:217340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0002230	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0003196	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0004209	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217340	17q21.31 microduplication syndrome		HP:0007018	ORPHA:217340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0011001	ORPHA:166119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0011849	ORPHA:166119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0040068	ORPHA:166119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0004289	ORPHA:166119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0009106	ORPHA:166119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0011314	ORPHA:166119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0040163	ORPHA:166119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0100774	ORPHA:166119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0100925	ORPHA:166119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0000620	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0001376	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0001387	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0001474	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0002653	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0002823	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0002829	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0004240	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0012758	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0030838	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0030840	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0030955	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0031051	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0032148	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0100569	ORPHA:166119	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0000077	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0000175	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0000818	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0001159	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0001627	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0002960	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0007417	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0010562	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166119	Isolated osteopoikilosis		HP:0100324	ORPHA:166119	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75325	Osteosclerosis-ichthyosis-premature ovarian failure syndrome		HP:0008064	ORPHA:75325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75325	Osteosclerosis-ichthyosis-premature ovarian failure syndrome		HP:0008209	ORPHA:75325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75325	Osteosclerosis-ichthyosis-premature ovarian failure syndrome		HP:0010741	ORPHA:75325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75325	Osteosclerosis-ichthyosis-premature ovarian failure syndrome		HP:0011001	ORPHA:75325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0000962	ORPHA:166113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0000982	ORPHA:166113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0001036	ORPHA:166113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0002664	ORPHA:166113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0008404	ORPHA:166113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0011367	ORPHA:166113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0040189	ORPHA:166113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0001903	ORPHA:166113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0008066	ORPHA:166113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0012034	ORPHA:166113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0100816	ORPHA:166113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0000956	ORPHA:166113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0000969	ORPHA:166113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0000989	ORPHA:166113	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166113	Bazex syndrome		HP:0030078	ORPHA:166113	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0000028	ORPHA:531151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0000126	ORPHA:531151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0001627	ORPHA:531151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0001288	ORPHA:531151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0002579	ORPHA:531151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0000508	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0000637	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0000750	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0001385	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0001883	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0002650	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0002714	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0003186	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0003422	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0007370	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0008897	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0012811	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0030809	ORPHA:531151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0000729	ORPHA:531151	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0001250	ORPHA:531151	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0001363	ORPHA:531151	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0002282	ORPHA:531151	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0003396	ORPHA:531151	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531151	9q21.13 microdeletion syndrome		HP:0010442	ORPHA:531151	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001627	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001629	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001635	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001643	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001659	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001712	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0002094	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0002875	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0031664	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0031668	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0032092	ORPHA:3092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001279	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001640	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001642	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001647	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001653	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001671	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001680	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001681	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0001962	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0004757	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0004970	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0006689	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0006695	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0012764	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0030950	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0030973	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3092	Fixed subaortic stenosis		HP:0100749	ORPHA:3092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0001650	ORPHA:3093	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0002875	ORPHA:3093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0030148	ORPHA:3093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0001712	ORPHA:3093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0004380	ORPHA:3093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0005135	ORPHA:3093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0005176	ORPHA:3093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0010883	ORPHA:3093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0025075	ORPHA:3093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0001681	ORPHA:3093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0001706	ORPHA:3093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0005162	ORPHA:3093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0012664	ORPHA:3093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0030850	ORPHA:3093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0100584	ORPHA:3093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0001645	ORPHA:3093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3093	Congenital aortic valve stenosis		HP:0012727	ORPHA:3093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0008058	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0008936	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0011471	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0012448	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0012736	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0030211	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0002169	ORPHA:423479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0003487	ORPHA:423479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0006579	ORPHA:423479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0010536	ORPHA:423479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0030921	ORPHA:423479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0030927	ORPHA:423479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency	NOT	HP:0011903	ORPHA:423479	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0002187	ORPHA:423479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000268	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000316	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000369	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000407	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000430	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000490	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000543	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000556	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000577	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0000873	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0001116	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0001285	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0001511	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0001525	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0002069	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0002079	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0002509	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0004322	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0004639	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0006801	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423479	X-linked intellectual disability-limb spasticity-retinal dystrophy-arginine vasopressin deficiency		HP:0007965	ORPHA:423479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0003808	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0005484	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0011344	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0012719	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0032588	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0032807	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0045084	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0100703	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0200055	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0000748	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001256	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001319	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001337	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001510	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002123	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002194	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002650	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002808	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0007281	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0007328	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0012469	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0025269	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0025387	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0030215	ORPHA:3095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome	NOT	HP:0007824	ORPHA:3095	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0000713	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0000729	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0000817	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001249	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001250	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001288	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002353	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002360	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002371	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002376	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002793	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0004302	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0004305	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0011968	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0012171	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0100022	ORPHA:3095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0000723	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0012760	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001252	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001257	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001332	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0001773	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002066	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002186	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002300	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002505	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002540	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002876	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3095	Atypical Rett syndrome		HP:0002882	ORPHA:3095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000027	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000135	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000670	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000682	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000789	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001249	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001252	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001263	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002463	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0008734	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0008736	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0010807	ORPHA:96264	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000028	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000046	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000110	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000286	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000316	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000389	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000486	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000545	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000581	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000582	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000679	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000684	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000717	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000771	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001250	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001763	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002019	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002099	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002205	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002650	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002673	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002827	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002974	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0003042	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0004209	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001382	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0005930	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0007018	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0200021	ORPHA:96264	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000175	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000248	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000303	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000445	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000457	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000470	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000737	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0000744	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001337	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001360	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0001762	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002020	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002079	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002139	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0002204	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0004322	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0004936	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0005280	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0005978	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0008678	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0030680	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0100025	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96264	49,XXXXY syndrome		HP:0100962	ORPHA:96264	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000027	ORPHA:96263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000135	ORPHA:96263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000789	ORPHA:96263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001256	ORPHA:96263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001263	ORPHA:96263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002463	ORPHA:96263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0008734	ORPHA:96263	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000028	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000046	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000098	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000286	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000316	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000389	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000457	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000486	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000582	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000670	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000679	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000682	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000684	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000717	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000771	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001252	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001763	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002019	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002099	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002205	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002974	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0003042	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0004209	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001382	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0005930	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0007018	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0008736	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0010807	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0200021	ORPHA:96263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000023	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000110	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000175	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000248	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000303	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000324	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000470	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000581	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000737	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000739	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000750	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001250	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001337	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001513	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0001762	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002020	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002204	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002650	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002673	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0002827	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0004936	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0005978	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0000718	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0012433	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0030680	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96263	48,XXXY syndrome		HP:0100753	ORPHA:96263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0000062	ORPHA:3097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0000142	ORPHA:3097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0000148	ORPHA:3097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0000776	ORPHA:3097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0006703	ORPHA:3097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0011027	ORPHA:3097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0000028	ORPHA:3097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0002101	ORPHA:3097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0004383	ORPHA:3097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0008736	ORPHA:3097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0030010	ORPHA:3097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0100632	ORPHA:3097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0000085	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001629	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001631	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001636	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001643	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001650	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001669	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001680	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001696	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001710	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0001743	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0004736	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3097	Meacham syndrome		HP:0010772	ORPHA:3097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0000157	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0000175	ORPHA:3098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0000218	ORPHA:3098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0000252	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0000260	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0000347	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0000470	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0001061	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0001156	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0001177	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0001199	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0001376	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0001642	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0002808	ORPHA:3098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0002815	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0002827	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0031095	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0003312	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0004322	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0005280	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0005930	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0008905	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0009811	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0009882	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0011362	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3098	Rhizomelic syndrome, Urbach type		HP:0100543	ORPHA:3098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001252	ORPHA:88639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001270	ORPHA:88639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001332	ORPHA:88639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002013	ORPHA:88639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002344	ORPHA:88639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0000286	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0000486	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0000639	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001250	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001347	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001508	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001942	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002078	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002119	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002151	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002360	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002521	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0003287	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0003468	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0007370	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0011334	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0011968	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0012469	ORPHA:88639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0000028	ORPHA:88639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0000737	ORPHA:88639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001298	ORPHA:88639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002093	ORPHA:88639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002352	ORPHA:88639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0012697	ORPHA:88639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0001636	ORPHA:88639	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88639	Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency		HP:0002599	ORPHA:88639	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000159	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000212	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000218	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000280	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000343	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000494	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000974	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0001007	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0001382	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0001582	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0001763	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0002209	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0002650	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0011232	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0012724	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0040079	ORPHA:217335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000766	ORPHA:217335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000978	ORPHA:217335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0001537	ORPHA:217335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0001620	ORPHA:217335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0100543	ORPHA:217335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000028	ORPHA:217335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0000815	ORPHA:217335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0001156	ORPHA:217335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0002659	ORPHA:217335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0004942	ORPHA:217335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0008209	ORPHA:217335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217335	RIN2 syndrome		HP:0011003	ORPHA:217335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88637	Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome		HP:0000668	ORPHA:88637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88637	Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome		HP:0000815	ORPHA:88637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88637	Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome		HP:0001251	ORPHA:88637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88637	Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome		HP:0003429	ORPHA:88637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000750	ORPHA:411493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001347	ORPHA:411493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0002194	ORPHA:411493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0010862	ORPHA:411493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000430	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000431	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000520	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000527	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000637	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001249	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001250	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001257	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001263	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001276	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001290	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0001510	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0002421	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0002538	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0002553	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0007141	ORPHA:411493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000737	ORPHA:411493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0002363	ORPHA:411493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0009879	ORPHA:411493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0025405	ORPHA:411493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000486	ORPHA:411493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000505	ORPHA:411493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411493	Pontocerebellar hypoplasia type 10		HP:0000648	ORPHA:411493	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88635	Vacuolar myopathy with sarcoplasmic reticulum protein aggregates		HP:0003198	ORPHA:88635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88635	Vacuolar myopathy with sarcoplasmic reticulum protein aggregates		HP:0003236	ORPHA:88635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0000100	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0000246	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0000421	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0000708	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0000980	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001288	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001369	ORPHA:3099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001482	ORPHA:3099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001633	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001646	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001654	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001701	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0001945	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002017	ORPHA:3099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002019	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002027	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002039	ORPHA:3099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002072	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002076	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002093	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002103	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002167	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002380	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0002829	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0010318	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0010522	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0010526	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0010783	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0011675	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0012378	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0012733	ORPHA:3099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0012819	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0100248	ORPHA:3099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0100584	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0100749	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3099	Rheumatic fever		HP:0100776	ORPHA:3099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000365	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000366	ORPHA:897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000426	ORPHA:897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000430	ORPHA:897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000431	ORPHA:897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000478	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000504	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000506	ORPHA:897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000534	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0000664	ORPHA:897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0001103	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0001341	ORPHA:897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002019	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002027	ORPHA:897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002211	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002216	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002226	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002227	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002242	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0002251	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0005214	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0005599	ORPHA:897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:897	Waardenburg-Shah syndrome		HP:0007703	ORPHA:897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000252	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000271	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000365	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000446	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000494	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000506	ORPHA:896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000574	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0000581	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0001063	ORPHA:896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0001167	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0001249	ORPHA:896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0001258	ORPHA:896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0001387	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0001631	ORPHA:896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0002779	ORPHA:896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0002817	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0005048	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0010554	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0010804	ORPHA:896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0011364	ORPHA:896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0100490	ORPHA:896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:896	Waardenburg syndrome type 3		HP:0100750	ORPHA:896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0002333	ORPHA:168782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0002376	ORPHA:168782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0010864	ORPHA:168782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0001250	ORPHA:168782	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0000729	ORPHA:168782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0001268	ORPHA:168782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0007064	ORPHA:168782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0100851	ORPHA:168782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0000020	ORPHA:168782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0000733	ORPHA:168782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0012760	ORPHA:168782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0000739	ORPHA:168782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0001344	ORPHA:168782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0002607	ORPHA:168782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0007086	ORPHA:168782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168782	Childhood disintegrative disorder		HP:0000726	ORPHA:168782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000238	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000541	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000556	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000587	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000648	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001249	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001252	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001263	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001265	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001284	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001302	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001321	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001324	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001328	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001339	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001460	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0002119	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0002126	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0002269	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0002334	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0002536	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0003202	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0003560	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001302	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0007731	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0007973	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0010508	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0012400	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0040081	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0045040	ORPHA:899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000028	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000256	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000501	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000528	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000568	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001274	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001305	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001331	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0007957	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0008736	ORPHA:899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000175	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000176	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000193	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000252	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000358	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000369	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000411	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000482	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000518	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0000612	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:899	Walker-Warburg syndrome		HP:0001250	ORPHA:899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000023	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000028	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000047	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000179	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000202	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000308	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000316	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000340	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000400	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000414	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000431	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000486	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0000582	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0001176	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0001250	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0001376	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0001597	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0002162	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0002242	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0002650	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0002750	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0004209	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0008559	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0009882	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0010864	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0011304	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0011344	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0100335	ORPHA:3080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3080	Intellectual disability, Wolff type		HP:0100490	ORPHA:3080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000028	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000174	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000303	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000347	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000405	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000446	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000470	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000582	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000601	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000768	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0000772	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0001162	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0001249	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0001595	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0001770	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0001991	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0002007	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0002217	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0002808	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0004209	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0004299	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0004322	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0005930	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0006265	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0006610	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0008736	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0009738	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0009896	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0009906	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0010059	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0010508	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0010978	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0030056	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3082	Intellectual disability-polydactyly-uncombable hair syndrome		HP:0100840	ORPHA:3082	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000028	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000147	ORPHA:3085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000280	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000407	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000505	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000518	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000639	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000771	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000815	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000842	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000869	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000956	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0000958	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0001156	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0001249	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0001272	ORPHA:3085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0001513	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0001769	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0001831	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0002750	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0002808	ORPHA:3085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0003307	ORPHA:3085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0004322	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0005978	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0007703	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0008734	ORPHA:3085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3085	Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome		HP:0010562	ORPHA:3085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000939	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000953	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000963	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000978	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001007	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001050	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001058	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001061	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001065	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001324	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001626	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001888	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001956	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001974	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0002721	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0003154	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0004324	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0007126	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0008221	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0010284	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0012743	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0025017	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0025383	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0003118	ORPHA:96253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0003466	ORPHA:96253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0008291	ORPHA:96253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0012030	ORPHA:96253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000141	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000708	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000712	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000819	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000822	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0031891	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0040270	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0500011	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000716	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000725	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000869	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000876	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000979	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001297	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001658	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0002086	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0002209	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0002315	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0002354	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0002690	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0002953	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0011370	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0031284	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0031364	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0031589	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0031845	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0033505	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0200042	ORPHA:96253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000709	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0000726	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0001123	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0007807	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0010741	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0010885	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0011999	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0025269	ORPHA:96253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96253	Cushing disease		HP:0030200	ORPHA:96253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88629	Tritanopia		HP:0000479	ORPHA:88629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88629	Tritanopia		HP:0000552	ORPHA:88629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88629	Tritanopia		HP:0030584	ORPHA:88629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88629	Tritanopia		HP:0000613	ORPHA:88629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88629	Tritanopia		HP:0007663	ORPHA:88629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88629	Tritanopia		HP:0012043	ORPHA:88629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0012532	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0012785	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0030147	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0040132	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002607	ORPHA:88628	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0000518	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0001250	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0001284	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0001251	ORPHA:88628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002166	ORPHA:88628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0010831	ORPHA:88628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0000510	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0000572	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0000580	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0000662	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0001249	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0001288	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0001290	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002066	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0007737	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0040078	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0045010	ORPHA:88628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002143	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002194	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002403	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002579	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002650	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002754	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0002808	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0003394	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88628	Posterior column ataxia-retinitis pigmentosa syndrome		HP:0012385	ORPHA:88628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0000822	ORPHA:231632	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0003351	ORPHA:231632	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0011740	ORPHA:231632	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0002315	ORPHA:231632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0002900	ORPHA:231632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0006735	ORPHA:231632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0100615	ORPHA:231632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0200114	ORPHA:231632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0000360	ORPHA:231632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0000421	ORPHA:231632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0001324	ORPHA:231632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor		HP:0002018	ORPHA:231632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231632	Ectopic aldosterone-producing tumor	NOT	HP:0008256	ORPHA:231632	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:88621	Ichthyosis-prematurity syndrome		HP:0001622	ORPHA:88621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88621	Ichthyosis-prematurity syndrome		HP:0001880	ORPHA:88621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88621	Ichthyosis-prematurity syndrome		HP:0002643	ORPHA:88621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88621	Ichthyosis-prematurity syndrome		HP:0007549	ORPHA:88621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88621	Ichthyosis-prematurity syndrome		HP:0008064	ORPHA:88621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0025197	ORPHA:88630	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0025473	ORPHA:88630	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0000191	ORPHA:88630	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0001156	ORPHA:88630	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0001371	ORPHA:88630	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0001596	ORPHA:88630	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0030084	ORPHA:88630	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0000286	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0000316	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0000437	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0000612	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0000685	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0001159	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0001655	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0002650	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0004322	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0004467	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0009139	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0010306	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0012385	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0045039	ORPHA:88630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0001653	ORPHA:88630	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:88630	Terminal osseous dysplasia-pigmentary defects syndrome		HP:0001723	ORPHA:88630	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0005528	ORPHA:3088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0430048	ORPHA:3088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0000252	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0000541	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0001321	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0001510	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0001915	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0002745	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0007617	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0007898	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0008070	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0008404	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0012758	ORPHA:3088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0001250	ORPHA:3088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0001251	ORPHA:3088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0001531	ORPHA:3088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3088	Revesz syndrome		HP:0004334	ORPHA:3088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000028	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000158	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000164	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000179	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000189	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000256	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000280	ORPHA:3071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000286	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000293	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000358	ORPHA:3071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000470	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000474	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000486	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000563	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000682	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000951	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000956	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0000962	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001231	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001249	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001531	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001561	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001582	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001595	ORPHA:3071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001598	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001629	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001634	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001639	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001642	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001800	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001814	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0002020	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0002033	ORPHA:3071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0002120	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0002224	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0002750	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0004322	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0004690	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0005280	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0001382	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0007440	ORPHA:3071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0007477	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0008872	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0009465	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0009748	ORPHA:3071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0012740	ORPHA:3071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0100679	ORPHA:3071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3071	Costello syndrome		HP:0100729	ORPHA:3071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0000316	ORPHA:3074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0000337	ORPHA:3074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0000343	ORPHA:3074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0000445	ORPHA:3074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0000463	ORPHA:3074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0001249	ORPHA:3074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0002007	ORPHA:3074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0004209	ORPHA:3074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3074	Intellectual disability-short stature-hypertelorism syndrome		HP:0010669	ORPHA:3074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0002160	ORPHA:88618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0002910	ORPHA:88618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0003073	ORPHA:88618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0010901	ORPHA:88618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0010919	ORPHA:88618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0000486	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0000565	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0000708	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0000736	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001263	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001321	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001392	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001508	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001510	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001789	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001928	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001976	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001999	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0002079	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0002376	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0002421	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0003236	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0003429	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0003560	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0008151	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0008169	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0008947	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0011900	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0011996	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0012110	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0012448	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0030890	ORPHA:88618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0000164	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0000252	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001324	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001402	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001638	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0001763	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0002119	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0002878	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0003235	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0007141	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0010719	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency		HP:0012704	ORPHA:88618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001259	ORPHA:88619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002922	ORPHA:88619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0006846	ORPHA:88619	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001249	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001250	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001257	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001260	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001276	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001288	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0001945	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002013	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002063	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002171	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002181	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002363	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002376	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002510	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0002793	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0003324	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0010663	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0011887	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0012747	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0025404	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88619	Familial acute necrotizing encephalopathy		HP:0031982	ORPHA:88619	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000194	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000268	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000289	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000322	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000338	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000341	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000347	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000411	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000446	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000455	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000752	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0000960	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0001263	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0001290	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0001319	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0001618	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0002015	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0002553	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0002705	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0010804	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0011081	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0011968	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0012471	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0030197	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0030200	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0040288	ORPHA:166108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0001284	ORPHA:166108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0001308	ORPHA:166108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0005060	ORPHA:166108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0005879	ORPHA:166108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0007002	ORPHA:166108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0007269	ORPHA:166108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166108	Birk-Barel syndrome		HP:0008366	ORPHA:166108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000272	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001156	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001230	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001249	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001769	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001783	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001831	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0003196	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0005280	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0006009	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0009803	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0010049	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0010055	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0010743	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0012368	ORPHA:439822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000280	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000303	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000322	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000327	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001511	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0005616	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0008897	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0010579	ORPHA:439822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000028	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000047	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000219	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000248	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000283	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000316	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000343	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000347	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000358	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000365	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000448	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000505	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000508	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000540	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000565	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000601	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000637	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000682	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0000729	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001250	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001319	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001382	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001513	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0001763	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0002003	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0002007	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0002516	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0002615	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0002684	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0003165	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0003301	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0005274	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0005819	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0008457	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0009824	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0010665	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439822	PDE4D haploinsufficiency syndrome		HP:0045025	ORPHA:439822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0002814	ORPHA:542643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0033260	ORPHA:542643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0200042	ORPHA:542643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0000953	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0000965	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001058	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001075	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001581	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001903	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001977	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0002619	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0002960	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0003029	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0003565	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0005339	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0007572	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0010741	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0012514	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0025016	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0100585	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0100724	ORPHA:542643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0000819	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0000822	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001760	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001976	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0002160	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0003119	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0003401	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0003493	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0004855	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0005293	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0005543	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0025343	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0030350	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0031190	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0031364	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0031365	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0032018	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0040224	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0040248	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0100963	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0410008	ORPHA:542643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001876	ORPHA:542643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001901	ORPHA:542643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0001974	ORPHA:542643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0002140	ORPHA:542643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0002725	ORPHA:542643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0012393	ORPHA:542643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542643	Livedoid vasculopathy		HP:0100647	ORPHA:542643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000162	ORPHA:166100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000175	ORPHA:166100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000272	ORPHA:166100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000343	ORPHA:166100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000347	ORPHA:166100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000407	ORPHA:166100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000767	ORPHA:166100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0000768	ORPHA:166100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0002758	ORPHA:166100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0002829	ORPHA:166100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0005916	ORPHA:166100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166100	Autosomal dominant otospondylomegaepiphyseal dysplasia		HP:0100777	ORPHA:166100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0000053	ORPHA:3077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0000718	ORPHA:3077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0000737	ORPHA:3077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0000752	ORPHA:3077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0001250	ORPHA:3077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002360	ORPHA:3077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0006801	ORPHA:3077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0001337	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0001635	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002039	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002061	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002342	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002395	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0004322	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0000718	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0007302	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0010864	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0011188	ORPHA:3077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0001297	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0001300	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0001513	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002136	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002322	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002362	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0002751	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0025403	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3077	X-linked intellectual disability-psychosis-macroorchidism syndrome		HP:0100852	ORPHA:3077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000252	ORPHA:3078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000648	ORPHA:3078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001250	ORPHA:3078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001276	ORPHA:3078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0008850	ORPHA:3078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0012715	ORPHA:3078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000618	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001257	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001518	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0002198	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0002788	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0005486	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0005949	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0010864	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0012444	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0040288	ORPHA:3078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000076	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000239	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000347	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000377	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0000400	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001199	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001305	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001321	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001336	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001374	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001629	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001838	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0001848	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0003196	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0005781	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0006829	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0006956	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3078	Severe X-linked intellectual disability, Gustavson type		HP:0008110	ORPHA:3078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000218	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000252	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000303	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000316	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000340	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000400	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000431	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000494	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000613	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000689	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000768	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0001231	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0001249	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0001537	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0001671	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0002064	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0002167	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0002213	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0002644	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0002683	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0004209	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0004322	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0004349	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0004422	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0006482	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0008407	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0008425	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0010807	ORPHA:3079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000126	ORPHA:3079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3079	Intellectual disability, Buenos-Aires type		HP:0000581	ORPHA:3079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0001288	ORPHA:98895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0002913	ORPHA:98895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0003236	ORPHA:98895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0003326	ORPHA:98895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0003546	ORPHA:98895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0003551	ORPHA:98895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0012086	ORPHA:98895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0001324	ORPHA:98895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0002527	ORPHA:98895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0002814	ORPHA:98895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0002910	ORPHA:98895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0003394	ORPHA:98895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0012378	ORPHA:98895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0001763	ORPHA:98895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0003202	ORPHA:98895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98895	Becker muscular dystrophy		HP:0030051	ORPHA:98895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0000750	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0001263	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0001270	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0001328	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0001371	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0001638	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0002093	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0002515	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0002650	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0003202	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0003236	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0003323	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0003701	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0008981	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98896	Duchenne muscular dystrophy		HP:0100543	ORPHA:98896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0000301	ORPHA:98897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0000590	ORPHA:98897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0000597	ORPHA:98897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0001824	ORPHA:98897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0007838	ORPHA:98897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0008376	ORPHA:98897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0030319	ORPHA:98897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0000183	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0000218	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0001604	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0002058	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0002100	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0002705	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0002747	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0007149	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0008756	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0008944	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0009053	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0009063	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0031162	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0200136	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0430015	ORPHA:98897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0000408	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0001284	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0002091	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0001288	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0002505	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0008959	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0008963	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0009027	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0009073	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0030192	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:3000005	ORPHA:98897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0008997	ORPHA:98897	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:0010550	ORPHA:98897	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98897	Oculopharyngodistal myopathy		HP:3000010	ORPHA:98897	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000252	ORPHA:391307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0001263	ORPHA:391307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0001999	ORPHA:391307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0010864	ORPHA:391307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000708	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000718	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000733	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000750	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0002360	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0002650	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0002751	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0004322	ORPHA:391307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000164	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000233	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000340	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000400	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000448	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000486	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000490	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000664	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000737	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0000752	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0001888	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0002079	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0002342	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0002486	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0002500	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0004691	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391307	Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome		HP:0008209	ORPHA:391307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0001279	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0001635	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0002027	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0002094	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0002321	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0011675	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0011710	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:871	Hereditary progressive cardiac conduction defect		HP:0012722	ORPHA:871	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000248	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000286	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000470	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000474	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000582	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001156	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001249	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001252	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001328	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001382	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0005280	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0011897	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0012368	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0100830	ORPHA:870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000144	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000158	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000160	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000164	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000179	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000189	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000194	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000235	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000457	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000475	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000691	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001513	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001537	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001629	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001852	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001871	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001873	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001901	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002247	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002376	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002511	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002714	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0003196	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0004209	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0004322	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0006695	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0007495	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0007598	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0010808	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0010978	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0030680	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0100763	ORPHA:870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000405	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000486	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000498	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000518	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000545	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000563	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000646	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000823	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001250	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001288	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001636	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001684	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0001909	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002020	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002023	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002251	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002608	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0002750	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0003414	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0005978	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0006733	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0007328	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0008070	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0008678	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0012450	ORPHA:870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:870	Down syndrome		HP:0000836	ORPHA:870	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0030499	ORPHA:75376	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0030500	ORPHA:75376	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0000572	ORPHA:75376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0007754	ORPHA:75376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0007937	ORPHA:75376	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0007703	ORPHA:75376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0011509	ORPHA:75376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0012508	ORPHA:75376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0030629	ORPHA:75376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0030631	ORPHA:75376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0030632	ORPHA:75376	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0000613	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0007401	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0007793	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0007950	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0011506	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0012231	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0025574	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0030528	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75376	Familial drusen		HP:0031526	ORPHA:75376	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0000126	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0001376	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0001482	ORPHA:873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0002024	ORPHA:873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0002027	ORPHA:873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0002239	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0002797	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0002829	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0003011	ORPHA:873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0003326	ORPHA:873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0004298	ORPHA:873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0005214	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0007703	ORPHA:873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0008069	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0010614	ORPHA:873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0010935	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0100245	ORPHA:873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0100749	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0100806	ORPHA:873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:873	Desmoid tumor		HP:0200008	ORPHA:873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75373	Progressive bifocal chorioretinal atrophy		HP:0000505	ORPHA:75373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75373	Progressive bifocal chorioretinal atrophy		HP:0000545	ORPHA:75373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75373	Progressive bifocal chorioretinal atrophy		HP:0000565	ORPHA:75373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75373	Progressive bifocal chorioretinal atrophy		HP:0000580	ORPHA:75373	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75373	Progressive bifocal chorioretinal atrophy		HP:0000639	ORPHA:75373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75373	Progressive bifocal chorioretinal atrophy		HP:0001135	ORPHA:75373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75373	Progressive bifocal chorioretinal atrophy		HP:0007401	ORPHA:75373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75374	Bradyopsia		HP:0000505	ORPHA:75374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75374	Bradyopsia		HP:0000613	ORPHA:75374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002751	ORPHA:3063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000175	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000179	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000275	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000276	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000324	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000939	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001166	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001519	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001611	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002317	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002808	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0003199	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0008947	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0010511	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0011308	ORPHA:3063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000028	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000029	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000047	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000160	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000218	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000316	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000319	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000369	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000414	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000426	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000463	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000465	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000582	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000664	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000678	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000750	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001256	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001336	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001344	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001999	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002123	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002353	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002540	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002757	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0003698	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0004305	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0007509	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0007687	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0010722	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0011153	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0045075	ORPHA:3063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000086	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000232	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000248	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000303	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000322	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000378	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000385	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000391	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000520	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000767	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0000768	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0001355	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002181	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0002187	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0004322	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0006610	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0010789	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0011003	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3063	X-linked intellectual disability, Snyder type		HP:0012385	ORPHA:3063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000252	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000278	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000325	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000426	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0001270	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0001999	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0002172	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0008947	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0011094	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0011343	ORPHA:319171	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000218	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000341	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000411	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0000490	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0001166	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0002761	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0002996	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0005469	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0005922	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0006927	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0010501	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0010669	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319171	Distal 17p13.1 microdeletion syndrome		HP:0010850	ORPHA:319171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0001263	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0001508	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0001511	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0001638	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0002059	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0002093	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0002151	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0003236	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0008872	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0008947	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0011923	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0012622	ORPHA:324525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0001250	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0001947	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0002490	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0002521	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0003348	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0003535	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0004322	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324525	Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation		HP:0011924	ORPHA:324525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0001263	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0001508	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0001744	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002110	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002205	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002716	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002720	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0004322	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0005387	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0008348	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0010976	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0011956	ORPHA:693681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0000509	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002014	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002024	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002240	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0002960	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0005411	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0032163	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0032204	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693681	Activated PI3K-delta syndrome 2		HP:0032247	ORPHA:693681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000039	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000175	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000180	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000191	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000243	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000252	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000308	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000340	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000358	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000414	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000465	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000470	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000480	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000506	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0000582	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001162	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001249	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001252	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001263	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001305	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001338	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001629	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001643	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001830	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0001999	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0002079	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0002198	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0002419	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0007082	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0007165	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0008689	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0008753	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0010051	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0010055	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0010066	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0010297	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0010535	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0011069	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0011471	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0011802	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0012447	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:434179	Orofaciodigital syndrome type 14		HP:0100954	ORPHA:434179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:868	Triose phosphate-isomerase deficiency		HP:0000762	ORPHA:868	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:868	Triose phosphate-isomerase deficiency		HP:0001252	ORPHA:868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:868	Triose phosphate-isomerase deficiency		HP:0001639	ORPHA:868	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:868	Triose phosphate-isomerase deficiency		HP:0003202	ORPHA:868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:868	Triose phosphate-isomerase deficiency		HP:0006597	ORPHA:868	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:868	Triose phosphate-isomerase deficiency		HP:0007009	ORPHA:868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:868	Triose phosphate-isomerase deficiency		HP:0010978	ORPHA:868	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:867	Familial multiple trichoepithelioma		HP:0001482	ORPHA:867	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:867	Familial multiple trichoepithelioma		HP:0002671	ORPHA:867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:867	Familial multiple trichoepithelioma		HP:0100585	ORPHA:867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:867	Familial multiple trichoepithelioma		HP:0200034	ORPHA:867	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000044	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000174	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000316	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000494	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000508	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000545	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000597	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0001519	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0002231	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0002750	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0003202	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0003307	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0004209	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0004303	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0004322	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0004493	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0008736	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0010628	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0010864	ORPHA:3068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000252	ORPHA:3068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000411	ORPHA:3068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000426	ORPHA:3068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0001376	ORPHA:3068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0003272	ORPHA:3068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000324	ORPHA:3068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000377	ORPHA:3068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000768	ORPHA:3068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0000772	ORPHA:3068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0002575	ORPHA:3068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3068	Intellectual disability-myopathy-short stature-endocrine defect syndrome		HP:0030680	ORPHA:3068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0000982	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001531	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001611	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001824	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001943	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0002013	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0002173	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0002615	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0003154	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0004322	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0008163	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0000522	ORPHA:869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0000846	ORPHA:869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0002571	ORPHA:869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0007440	ORPHA:869	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0008872	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0012735	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0031078	ORPHA:869	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0000252	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0000407	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0000505	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0000648	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001097	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001249	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001251	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001252	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001347	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0001761	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0002093	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0002376	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0007002	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0007556	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0010486	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0012804	ORPHA:869	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:869	Triple A syndrome		HP:0004319	ORPHA:869	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000282	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000969	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001265	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001324	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0002018	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0003212	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0003457	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0030953	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0100539	ORPHA:863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000211	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000360	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000496	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000509	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000602	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000708	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000737	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000741	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000988	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001254	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001262	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001269	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001289	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001626	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0002015	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0002321	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0002354	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0002921	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0004372	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0005986	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0200026	ORPHA:863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000553	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000573	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000587	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0000651	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001287	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0001298	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0002301	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0002381	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0003487	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0009916	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0010628	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:863	Trichinellosis		HP:0025342	ORPHA:863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0000961	ORPHA:860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001649	ORPHA:860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001693	ORPHA:860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0011028	ORPHA:860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0011563	ORPHA:860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0012418	ORPHA:860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0030148	ORPHA:860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0000975	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001508	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001629	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001631	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001633	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001635	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001640	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001641	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001643	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001667	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0002789	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0006704	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0010772	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0012303	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0025074	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0031348	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0031349	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0032092	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0200128	ORPHA:860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001518	ORPHA:860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0001680	ORPHA:860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0002240	ORPHA:860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0011611	ORPHA:860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0012304	ORPHA:860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0009800	ORPHA:860	TAS		HP:0040284			H	ORPHA:orphadata[2025-10-22]
ORPHA:860	Congenitally uncorrected transposition of the great arteries		HP:0011438	ORPHA:860	TAS		HP:0040284			H	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000046	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000143	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000154	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000160	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000162	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000175	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000204	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000218	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000248	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000316	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000384	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000453	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000518	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000568	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000643	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000682	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000778	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000834	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000925	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0001263	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0001508	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0001643	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0002006	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0002084	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0002093	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0002381	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0002575	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0005701	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0005990	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0006482	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0008736	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0008872	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0009554	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0009795	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0011481	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0030680	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000272	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000278	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000327	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000347	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000494	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0001999	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0002652	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0004348	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0010669	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0010807	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0011219	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0011800	ORPHA:861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000164	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000294	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000356	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000358	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000370	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000405	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000413	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000431	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000486	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000505	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000561	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000612	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000625	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000689	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000750	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0002007	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0008551	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0009804	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0011386	ORPHA:861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:861	Treacher-Collins syndrome		HP:0000028	ORPHA:861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000154	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000232	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000233	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000252	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000319	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000325	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000343	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000463	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001156	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0005916	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001249	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001263	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001328	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001373	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001596	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002300	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002381	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002705	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0004279	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0008070	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0009928	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0010529	ORPHA:3051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000028	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000035	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000446	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000527	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000581	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000964	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001167	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001250	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0001852	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002121	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002133	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002553	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002650	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0003510	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0006610	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0007392	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0007665	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0009836	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0010720	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0011097	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0012745	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0100760	ORPHA:3051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0000494	ORPHA:3051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0002750	ORPHA:3051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0005616	ORPHA:3051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0005930	ORPHA:3051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0030680	ORPHA:3051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3051	Nicolaides-Baraitser syndrome		HP:0100790	ORPHA:3051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0007642	ORPHA:75382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0007984	ORPHA:75382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0030824	ORPHA:75382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000539	ORPHA:75382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000545	ORPHA:75382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000608	ORPHA:75382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000486	ORPHA:75382	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000505	ORPHA:75382	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000510	ORPHA:75382	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000639	ORPHA:75382	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease		HP:0000651	ORPHA:75382	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease	NOT	HP:0001123	ORPHA:75382	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:75382	Oguchi disease	NOT	HP:0007641	ORPHA:75382	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3052	X-linked intellectual disability-seizures-psoriasis syndrome		HP:0001249	ORPHA:3052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3052	X-linked intellectual disability-seizures-psoriasis syndrome		HP:0001250	ORPHA:3052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3052	X-linked intellectual disability-seizures-psoriasis syndrome		HP:0003765	ORPHA:3052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3052	X-linked intellectual disability-seizures-psoriasis syndrome	NOT	HP:0003538	ORPHA:3052	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3052	X-linked intellectual disability-seizures-psoriasis syndrome	NOT	HP:0008064	ORPHA:3052	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000026	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000027	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000119	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000243	ORPHA:99330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000262	ORPHA:99330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000280	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000316	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000347	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000358	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000394	ORPHA:99330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000519	ORPHA:99330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000708	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000744	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000750	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0001263	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000771	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0003241	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0000837	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002750	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0001176	ORPHA:99330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0009237	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0001249	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0001252	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0001999	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002119	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002500	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002650	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002761	ORPHA:99330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002788	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002967	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0002974	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0003782	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0003946	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0004237	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0008193	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0008734	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0011310	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0011343	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0040019	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0040171	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0045058	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0100559	ORPHA:99330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99330	49,XYYYY syndrome		HP:0100710	ORPHA:99330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0008959	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0009046	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0010628	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0012391	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0003803	ORPHA:178145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0004976	ORPHA:178145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0005001	ORPHA:178145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0001319	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0001762	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0002194	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0003324	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0003327	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0001382	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178145	Moderate multiminicore disease with hand involvement		HP:0008954	ORPHA:178145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000232	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000272	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000280	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000316	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000463	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000750	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001252	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001263	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002263	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0003196	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0010804	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0010864	ORPHA:261494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000158	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000248	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000252	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000303	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000337	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000365	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000389	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000391	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000582	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000664	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000708	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000718	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000729	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000742	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001513	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001629	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001647	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001680	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002019	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002360	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002553	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0011675	ORPHA:261494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000028	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000047	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000054	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000076	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000083	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000107	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000126	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000324	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000684	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0000733	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001250	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001274	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001376	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001636	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0001762	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002020	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002021	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002094	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002119	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002120	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002205	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002376	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002558	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002607	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002650	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002714	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0002779	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0004322	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0004415	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0006288	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0008736	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0100716	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261494	Kleefstra syndrome		HP:0100790	ORPHA:261494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000028	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000218	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000268	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000369	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000426	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000465	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000470	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0000954	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0001371	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0001591	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0002093	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0002194	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0002650	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0002792	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0002804	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0003327	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0003789	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0008050	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0030084	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0100297	ORPHA:178148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178148	Antenatal multiminicore disease with arthrogryposis multiplex congenita		HP:0002808	ORPHA:178148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0000822	ORPHA:231625	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0100631	ORPHA:231625	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0001324	ORPHA:231625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0002900	ORPHA:231625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0003118	ORPHA:231625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0003351	ORPHA:231625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0011740	ORPHA:231625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0200114	ORPHA:231625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0001962	ORPHA:231625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0002018	ORPHA:231625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0003081	ORPHA:231625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0003394	ORPHA:231625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0003401	ORPHA:231625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0005135	ORPHA:231625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0000360	ORPHA:231625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0000421	ORPHA:231625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0002170	ORPHA:231625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231625	Adrenocortical carcinoma with pure aldosterone hypersecretion		HP:0002315	ORPHA:231625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0000718	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0000729	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0000750	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0000752	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0001252	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0001257	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0002342	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0002360	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0003763	ORPHA:356996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0000256	ORPHA:356996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0001250	ORPHA:356996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0001256	ORPHA:356996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:356996	ANK3-related intellectual disability-sleep disturbance syndrome		HP:0001520	ORPHA:356996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000143	ORPHA:857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000384	ORPHA:857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001177	ORPHA:857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001199	ORPHA:857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0002023	ORPHA:857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0004792	ORPHA:857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000377	ORPHA:857	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000028	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000083	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000365	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000396	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001482	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001545	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001760	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001763	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001863	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0002019	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0004209	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0008551	ORPHA:857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000047	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000048	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000076	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000086	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000089	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000130	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000142	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000154	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000324	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000486	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000504	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000518	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000567	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000568	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000581	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000612	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000772	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000821	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0000823	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001140	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001249	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001274	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001508	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001631	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001636	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001641	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001643	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001671	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0001770	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0002308	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0002607	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0003468	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0004322	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0005562	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0006824	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0008736	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0009465	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0009912	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0009944	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0010059	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0010331	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0010481	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0010760	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0011304	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0012210	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0030680	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:857	Townes-Brocks syndrome		HP:0100559	ORPHA:857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000028	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000358	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000486	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000506	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000708	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0001249	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0001250	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0001263	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0001513	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0001608	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0004322	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0008736	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0010468	ORPHA:3055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0008064	ORPHA:3055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000639	ORPHA:3055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000964	ORPHA:3055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0000992	ORPHA:3055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3055	X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome		HP:0004299	ORPHA:3055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000026	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000027	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000098	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000179	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000218	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000286	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000316	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000343	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000470	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000708	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000718	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000744	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0000750	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0001263	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0012210	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0001061	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0001249	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0001256	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0001760	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0001763	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0002099	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0002788	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0002974	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0003083	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0005280	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0006297	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0006316	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0007477	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0008193	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0011968	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99329	48,XYYY syndrome		HP:0100710	ORPHA:99329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0001873	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0001875	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0001876	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0001888	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0001919	ORPHA:859	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0001980	ORPHA:859	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0002720	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0002850	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0003220	ORPHA:859	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0004313	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0004315	ORPHA:859	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:859	Transcobalamin deficiency		HP:0012120	ORPHA:859	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3057	Monoamine oxidase A deficiency		HP:0000708	ORPHA:3057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3057	Monoamine oxidase A deficiency		HP:0100543	ORPHA:3057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0000238	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0000252	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0000365	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0000505	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0000568	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0000639	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0000952	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001250	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001252	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001263	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001511	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001531	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001541	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001622	ORPHA:858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001640	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001873	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0001903	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0002014	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0002119	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0002240	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0002514	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0002716	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0002910	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0007703	ORPHA:858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0012733	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:858	Congenital toxoplasmosis		HP:0100543	ORPHA:858	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0004809	ORPHA:853	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0000967	ORPHA:853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0000979	ORPHA:853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0001892	ORPHA:853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0007420	ORPHA:853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0012541	ORPHA:853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0000790	ORPHA:853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0002170	ORPHA:853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0002239	ORPHA:853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0002249	ORPHA:853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0031364	ORPHA:853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0000618	ORPHA:853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0000707	ORPHA:853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0001263	ORPHA:853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0002138	ORPHA:853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0008619	ORPHA:853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:853	Fetal and neonatal alloimmune thrombocytopenia		HP:0100021	ORPHA:853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0030631	ORPHA:75377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0031152	ORPHA:75377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0000505	ORPHA:75377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0000572	ORPHA:75377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0007401	ORPHA:75377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0007663	ORPHA:75377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0007894	ORPHA:75377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0007924	ORPHA:75377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0030615	ORPHA:75377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0000533	ORPHA:75377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0007814	ORPHA:75377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0007980	ORPHA:75377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0011510	ORPHA:75377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0030491	ORPHA:75377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0030629	ORPHA:75377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0000662	ORPHA:75377	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75377	Central areolar choroidal dystrophy		HP:0007641	ORPHA:75377	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75378	Oligocone trichromacy		HP:0000512	ORPHA:75378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75378	Oligocone trichromacy		HP:0000613	ORPHA:75378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000028	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000062	ORPHA:893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000232	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000252	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000347	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000364	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000501	ORPHA:893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000505	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000508	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000518	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0000639	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0001249	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0001513	ORPHA:893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0002650	ORPHA:893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0004322	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0007299	ORPHA:893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0008053	ORPHA:893	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:893	WAGR syndrome		HP:0100627	ORPHA:893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0000478	ORPHA:892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0000822	ORPHA:892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0005584	ORPHA:892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0006748	ORPHA:892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0006880	ORPHA:892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0009711	ORPHA:892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0011976	ORPHA:892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0000572	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0000739	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0000975	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0000980	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001085	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001095	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001297	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001638	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001737	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001962	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0002027	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0002315	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0002321	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0003334	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0003418	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0003484	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0005162	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0005562	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0008261	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0009053	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0009715	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0009763	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0011675	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0030393	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0030405	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0040049	ORPHA:892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0000541	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001658	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0001901	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0002516	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0002668	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0002894	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0012819	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:892	Von Hippel-Lindau disease		HP:0030424	ORPHA:892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0000365	ORPHA:895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0002216	ORPHA:895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0005599	ORPHA:895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0000407	ORPHA:895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0001053	ORPHA:895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0001100	ORPHA:895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0002211	ORPHA:895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0000077	ORPHA:895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0000506	ORPHA:895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0000508	ORPHA:895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0002251	ORPHA:895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:895	Waardenburg syndrome type 2		HP:0004414	ORPHA:895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000303	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000365	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000478	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000504	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000506	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000574	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000632	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0001053	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0001100	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002211	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002226	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002227	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0003196	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0005599	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0008527	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0011364	ORPHA:894	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000430	ORPHA:894	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000431	ORPHA:894	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000664	ORPHA:894	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0001595	ORPHA:894	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002216	ORPHA:894	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0010804	ORPHA:894	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000175	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000204	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000486	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000508	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0000912	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002251	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002414	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002435	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0002650	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:894	Waardenburg syndrome type 1		HP:0030680	ORPHA:894	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0000565	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0000938	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0001250	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0001290	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0001337	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0001397	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0001508	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0002019	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0002020	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0002167	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0002910	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0003256	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0003429	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0003642	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0004322	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0005616	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0007301	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0012758	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0410018	ORPHA:300536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0000958	ORPHA:300536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0009125	ORPHA:300536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0000832	ORPHA:300536	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300536	DDOST-CDG		HP:0012593	ORPHA:300536	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001761	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001831	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001840	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001956	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002205	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002313	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002378	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002938	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002942	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002944	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0004691	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0004692	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0005469	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0008414	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0009738	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0011220	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0011800	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0011968	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0030044	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000232	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000233	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000348	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000455	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000490	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000582	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001999	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002234	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002292	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0003086	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0010864	ORPHA:3041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000054	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000135	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000219	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000414	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000635	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001250	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002317	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0002751	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0003065	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0003199	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0003241	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0003758	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0008734	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0008947	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0010499	ORPHA:3041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000218	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000268	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000286	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000322	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000411	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000742	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0000957	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001187	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3041	Intellectual disability-balding-patella luxation-acromicria syndrome		HP:0001310	ORPHA:3041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000135	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000174	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000238	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000400	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000405	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000494	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000518	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000664	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000767	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000771	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0000774	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0001249	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0001250	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0001288	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0001357	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0001371	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0001798	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0001903	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0002376	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0002650	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0002797	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0002808	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0002868	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0003198	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0003273	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0003301	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0003312	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0004322	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0005103	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0005121	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0008689	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0011800	ORPHA:3042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3042	Intellectual disability-cataracts-calcified pinnae-myopathy syndrome		HP:0012062	ORPHA:3042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0007773	ORPHA:891	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0007685	ORPHA:891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0001493	ORPHA:891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0007663	ORPHA:891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0007917	ORPHA:891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0012795	ORPHA:891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0030666	ORPHA:891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0031526	ORPHA:891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0000252	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0000365	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0000518	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0000533	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0000568	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0000618	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0001004	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0001141	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0001256	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0001270	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0004349	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0007902	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0011342	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0012230	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0030496	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0030503	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0040049	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0100014	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:891	Familial exudative vitreoretinopathy		HP:0100832	ORPHA:891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0000083	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0000952	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0001541	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0002027	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0002240	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0002878	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0002910	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0003573	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0004324	ORPHA:890	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0001928	ORPHA:890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0003645	ORPHA:890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:890	Hepatic veno-occlusive disease		HP:0002480	ORPHA:890	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0002205	ORPHA:693661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0001744	ORPHA:693661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0002110	ORPHA:693661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0002240	ORPHA:693661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0002716	ORPHA:693661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0002960	ORPHA:693661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0010976	ORPHA:693661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0011956	ORPHA:693661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0000509	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0000620	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0001263	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0002014	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0002024	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0004322	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0005401	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0011110	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0020114	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0032163	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0032204	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0032247	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0200043	ORPHA:693661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:693661	Activated PI3K-delta syndrome 1		HP:0031699	ORPHA:693661	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0000028	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0000135	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0000233	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0000414	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0000490	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001256	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001263	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001508	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001620	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001773	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0004322	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0008734	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0200055	ORPHA:261483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0000771	ORPHA:261483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001252	ORPHA:261483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001511	ORPHA:261483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0001956	ORPHA:261483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0002231	ORPHA:261483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261483	Xq27.3q28 duplication syndrome		HP:0002750	ORPHA:261483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0002148	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0002150	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0003109	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0004912	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0010639	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0031415	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0031425	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0031428	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0031817	ORPHA:157215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0000787	ORPHA:157215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0000924	ORPHA:157215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0001510	ORPHA:157215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0002653	ORPHA:157215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0002749	ORPHA:157215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0004349	ORPHA:157215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0012408	ORPHA:157215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0000897	ORPHA:157215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0002515	ORPHA:157215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0002756	ORPHA:157215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0002979	ORPHA:157215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157215	Hereditary hypophosphatemic rickets with hypercalciuria		HP:0004322	ORPHA:157215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168796	Heart-hand syndrome, Slovenian type		HP:0001644	ORPHA:168796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168796	Heart-hand syndrome, Slovenian type		HP:0001760	ORPHA:168796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168796	Heart-hand syndrome, Slovenian type		HP:0005115	ORPHA:168796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168796	Heart-hand syndrome, Slovenian type		HP:0005150	ORPHA:168796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168796	Heart-hand syndrome, Slovenian type		HP:0011675	ORPHA:168796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168796	Heart-hand syndrome, Slovenian type		HP:0011702	ORPHA:168796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168796	Heart-hand syndrome, Slovenian type		HP:0001156	ORPHA:168796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0000276	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0000303	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0000445	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0000490	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0001263	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0001999	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0002225	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0002342	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0003191	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0003782	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0008232	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0008734	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0011969	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0012809	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0040171	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0100651	ORPHA:3044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0002069	ORPHA:3044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0008947	ORPHA:3044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0100783	ORPHA:3044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0000327	ORPHA:3044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0002373	ORPHA:3044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3044	Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome		HP:0008988	ORPHA:3044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0000163	ORPHA:889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0000965	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0000979	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0000988	ORPHA:889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0001025	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0001482	ORPHA:889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0001581	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0001945	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0002633	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0002829	ORPHA:889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0003326	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0010783	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0100758	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:889	Cutaneous small vessel vasculitis		HP:0200034	ORPHA:889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000212	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000316	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000347	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000356	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000369	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000485	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000695	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000894	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0000938	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0001007	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0001156	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0001591	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0001978	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0003175	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0004440	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0004453	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0005474	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0007642	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0008665	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0010455	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0011223	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0011800	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0030042	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0030313	ORPHA:313855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0001433	ORPHA:313855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0002814	ORPHA:313855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313855	FGFR2-related bent bone dysplasia		HP:0002979	ORPHA:313855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000028	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000269	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000278	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000340	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000347	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000358	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000369	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000414	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000448	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000581	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000821	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001249	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001252	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001263	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001328	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0003189	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0003510	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0012745	ORPHA:3047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000176	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000193	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000252	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001250	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001508	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001510	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001561	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001629	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001631	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001643	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0002205	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0004209	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0004426	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0001382	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0005990	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0006695	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0007598	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0008188	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0008191	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0009738	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0011968	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0100028	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0100490	ORPHA:3047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0000614	ORPHA:3047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3047	Blepharophimosis-intellectual disability syndrome, SBBYS type		HP:0100648	ORPHA:3047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000407	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000505	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000512	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000529	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000618	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000662	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0001123	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0001751	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0007703	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0008568	ORPHA:886	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000518	ORPHA:886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000545	ORPHA:886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0001251	ORPHA:886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0008499	ORPHA:886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000360	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000483	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000639	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000670	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000682	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000691	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000709	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000716	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000738	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0000739	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0001639	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0002120	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0002194	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0002312	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0003198	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0003457	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0007360	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0007994	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0008947	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0010780	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0011025	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0011073	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:886	Usher syndrome		HP:0031936	ORPHA:886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0100267	ORPHA:888	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0000175	ORPHA:888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0000196	ORPHA:888	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0000193	ORPHA:888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0000204	ORPHA:888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0000668	ORPHA:888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0010286	ORPHA:888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:888	Van der Woude syndrome		HP:0010296	ORPHA:888	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001561	ORPHA:887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001622	ORPHA:887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0002023	ORPHA:887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0002777	ORPHA:887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0006703	ORPHA:887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000086	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000104	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000776	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001601	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001671	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0002575	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0003422	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0006501	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0030680	ORPHA:887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000003	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000008	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000028	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000047	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000048	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000062	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000126	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000175	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000239	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000358	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000772	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0000795	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001048	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001177	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001195	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001511	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001539	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0001732	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0002085	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0002323	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0005107	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0005108	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0005264	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0006101	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0008736	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0012732	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:887	VACTERL/VATER association		HP:0100335	ORPHA:887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:882	Tyrosinemia type 1		HP:0001402	ORPHA:882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:882	Tyrosinemia type 1		HP:0001744	ORPHA:882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:882	Tyrosinemia type 1		HP:0002240	ORPHA:882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:882	Tyrosinemia type 1		HP:0002909	ORPHA:882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:882	Tyrosinemia type 1		HP:0006463	ORPHA:882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:882	Tyrosinemia type 1		HP:0006554	ORPHA:882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002808	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002857	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002910	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0005113	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0005689	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0006438	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0006456	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0007477	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0009759	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0010044	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0010047	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0010510	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000085	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000086	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000164	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000286	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000476	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000486	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000508	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000545	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000716	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000767	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000842	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000987	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000995	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001004	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001045	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001231	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001385	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001395	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001596	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001631	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001647	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001657	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001658	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001680	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001763	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001812	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001831	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002608	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002611	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002650	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002960	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0003067	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0003186	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0003764	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0004349	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0005603	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0005978	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0007018	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000377	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0009118	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0011307	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0012434	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0100646	ORPHA:881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000150	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000471	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000133	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000137	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000470	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000823	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000837	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000879	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000938	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000939	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001510	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001511	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002750	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001394	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002037	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002613	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002647	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002861	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0004383	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0004386	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0005294	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0008678	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0012758	ORPHA:881	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002967	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0003492	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0004322	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0006610	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0006709	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0008209	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0008222	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0008897	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0012774	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0040072	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0100625	ORPHA:881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000218	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000278	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000347	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000365	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000369	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000403	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000465	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000474	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000475	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000708	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000739	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000758	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000786	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000822	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000869	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000872	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0000914	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001328	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001397	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001513	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001531	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001800	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001952	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0001999	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002162	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:881	Turner syndrome		HP:0002705	ORPHA:881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000215	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000219	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000232	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000343	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000470	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000508	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000684	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000966	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0001252	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0001315	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0002714	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0002750	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0004322	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0004326	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0001382	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0008070	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0010864	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0045075	ORPHA:884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000280	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000316	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000463	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000506	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000582	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0002007	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0003196	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0011220	ORPHA:884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0000486	ORPHA:884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0002023	ORPHA:884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:884	Pallister-Killian syndrome		HP:0100736	ORPHA:884	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000729	ORPHA:647799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000750	ORPHA:647799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001249	ORPHA:647799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001263	ORPHA:647799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0010862	ORPHA:647799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000293	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000414	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000490	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000718	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000733	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001270	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001328	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001513	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0002263	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0002342	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0002360	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0002591	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0007018	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0007874	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0008947	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0011443	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0012378	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0100710	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0100738	ORPHA:647799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000028	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000252	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000483	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000486	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000540	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000739	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000817	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001250	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001256	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001319	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001508	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001511	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001558	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001622	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0001998	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0002020	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0002098	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0002119	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0003763	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0004322	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0005988	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0008071	ORPHA:647799	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0008872	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0009800	ORPHA:647799	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0010864	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0025160	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0025502	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0032508	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:6000352	ORPHA:647799	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000054	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000107	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000135	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000256	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000545	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000639	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000657	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000776	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0000872	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0003077	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0010535	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0010952	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:647799	MYT1L-related developmental delay-intellectual disability-obesity syndrome		HP:0034977	ORPHA:647799	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000044	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000232	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000316	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000403	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000486	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000540	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000565	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001263	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000846	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0000939	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001249	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001250	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001257	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001259	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001274	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001319	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001289	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001382	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001510	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0001993	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0002017	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0002155	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0003198	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0003199	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0003236	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0008981	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0003738	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0003750	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0004349	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0005949	ORPHA:261476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0008207	ORPHA:261476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261476	Xp21 deletion syndrome		HP:0040019	ORPHA:261476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0000003	ORPHA:3032	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0000110	ORPHA:3032	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0001305	ORPHA:3032	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0001561	ORPHA:3032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0001562	ORPHA:3032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0001732	ORPHA:3032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0002089	ORPHA:3032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0002566	ORPHA:3032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0012440	ORPHA:3032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3032	NPHP3-related Meckel-like syndrome		HP:0030146	ORPHA:3032	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0006286	ORPHA:88661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0011073	ORPHA:88661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0005216	ORPHA:88661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0006285	ORPHA:88661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0006297	ORPHA:88661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0009102	ORPHA:88661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0011084	ORPHA:88661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0011085	ORPHA:88661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0025124	ORPHA:88661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0000679	ORPHA:88661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0000685	ORPHA:88661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0000687	ORPHA:88661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0006283	ORPHA:88661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0010299	ORPHA:88661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0011071	ORPHA:88661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:88661	Amelogenesis imperfecta		HP:0030791	ORPHA:88661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0000112	ORPHA:3033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0000114	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0000252	ORPHA:3033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0000316	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0001561	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0001562	ORPHA:3033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0001622	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0001636	ORPHA:3033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0002089	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0005562	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0001382	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0007598	ORPHA:3033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3033	Renal tubular dysgenesis		HP:0008660	ORPHA:3033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0007565	ORPHA:137605	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000708	ORPHA:137605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000997	ORPHA:137605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001328	ORPHA:137605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0030052	ORPHA:137605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000256	ORPHA:137605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000736	ORPHA:137605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000752	ORPHA:137605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000766	ORPHA:137605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001012	ORPHA:137605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0004322	ORPHA:137605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000365	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000518	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000750	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0000787	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001114	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001250	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001252	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001270	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001332	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001634	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0001642	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0002650	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0002667	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0004209	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0004845	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0006671	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0007018	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0007099	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0009588	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0010442	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0030358	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0032077	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0100245	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0100543	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0100615	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome		HP:0410263	ORPHA:137605	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome	NOT	HP:0001067	ORPHA:137605	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome	NOT	HP:0009734	ORPHA:137605	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome	NOT	HP:0009737	ORPHA:137605	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome	NOT	HP:0100006	ORPHA:137605	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:137605	Legius syndrome	NOT	HP:0100252	ORPHA:137605	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3034	Delayed membranous cranial ossification		HP:0000269	ORPHA:3034	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3034	Delayed membranous cranial ossification		HP:0000316	ORPHA:3034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3034	Delayed membranous cranial ossification		HP:0000457	ORPHA:3034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3034	Delayed membranous cranial ossification		HP:0000582	ORPHA:3034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3034	Delayed membranous cranial ossification		HP:0002007	ORPHA:3034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3034	Delayed membranous cranial ossification		HP:0004331	ORPHA:3034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3034	Delayed membranous cranial ossification		HP:0011800	ORPHA:3034	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0000347	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0000582	ORPHA:3035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0000772	ORPHA:3035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0001511	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0001539	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0001744	ORPHA:3035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002089	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002410	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002514	ORPHA:3035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002566	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002814	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002982	ORPHA:3035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002986	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0002991	ORPHA:3035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0006487	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0009816	ORPHA:3035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3035	Growth delay-hydrocephaly-lung hypoplasia syndrome		HP:0100569	ORPHA:3035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000218	ORPHA:3038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000316	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000324	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000343	ORPHA:3038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000369	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000463	ORPHA:3038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000486	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000494	ORPHA:3038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000508	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000577	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0000750	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0001249	ORPHA:3038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0007946	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3038	Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome		HP:0009908	ORPHA:3038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0000256	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0001482	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0001635	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0001883	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0002757	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0004349	ORPHA:137608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0004374	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0005293	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0007392	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0010566	ORPHA:137608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100013	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100026	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100031	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100559	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100560	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100615	ORPHA:137608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100761	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0100764	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137608	Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome		HP:0200034	ORPHA:137608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000194	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000327	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000431	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000457	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0001156	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0001249	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0001597	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0001831	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0003196	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0003312	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0004322	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0005280	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0005616	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0005916	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0010049	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0010579	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0010655	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0010743	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0011800	ORPHA:950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000028	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000055	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000248	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000303	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000316	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000365	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000463	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000506	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000684	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000940	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000944	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0001373	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002007	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002673	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002818	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002823	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002970	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002983	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002984	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0003022	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0003416	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0006059	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0006487	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0009830	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0010978	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0011220	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0040071	ORPHA:950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000135	ORPHA:950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000286	ORPHA:950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000858	ORPHA:950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0000995	ORPHA:950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0002650	ORPHA:950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0010807	ORPHA:950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:950	Acrodysostosis		HP:0012368	ORPHA:950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0100494	ORPHA:98850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0000939	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0000989	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001433	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001824	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001974	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002014	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002024	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002027	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002039	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002615	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002653	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002716	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002829	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0003155	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0012378	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0025142	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0031284	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0031408	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0031901	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0032155	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0100845	ORPHA:98850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001025	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001409	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001410	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001541	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001873	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001875	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001876	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001903	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001909	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0001971	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002239	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002756	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0002797	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0004377	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0008066	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0011121	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98850	Aggressive systemic mastocytosis		HP:0040186	ORPHA:98850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0000164	ORPHA:93160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0000268	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0000765	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0000787	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0000843	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0000944	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0000951	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0001288	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0001373	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0001596	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002007	ORPHA:93160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002148	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002650	ORPHA:93160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002653	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002749	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002757	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002797	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002857	ORPHA:93160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002901	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0002970	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0003272	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0003312	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0003330	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0004322	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0006323	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0009124	ORPHA:93160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0012062	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93160	Hypocalcemic vitamin D-resistant rickets		HP:0100670	ORPHA:93160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0001290	ORPHA:456328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000028	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000048	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000054	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000807	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000808	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0001561	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0002093	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0003244	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0040314	ORPHA:456328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000218	ORPHA:456328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000278	ORPHA:456328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0000883	ORPHA:456328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0001382	ORPHA:456328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456328	X-linked myotubular myopathy-abnormal genitalia syndrome		HP:0011968	ORPHA:456328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001288	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001332	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001392	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001409	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001413	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001744	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001901	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002040	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002063	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002067	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002075	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002172	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002240	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002345	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001288	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002453	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002910	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0009830	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0010927	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0012447	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0012751	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0040135	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0000252	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0000952	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001639	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001928	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002078	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002154	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002313	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0002446	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0004337	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0007010	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0008151	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0012343	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0025196	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0025321	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0100513	ORPHA:309854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0000338	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001260	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309854	Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome		HP:0001276	ORPHA:309854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000175	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000262	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000322	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000347	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000358	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000377	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000426	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000463	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000494	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000506	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000508	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000520	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0001182	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0001199	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0001231	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0002869	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0003312	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0004322	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0004467	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0008388	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0009882	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0010034	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0010097	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0011304	ORPHA:949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000252	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000316	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000340	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000405	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000407	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000453	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000545	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000632	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0000767	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0001363	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0002673	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0002857	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0003272	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0003298	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0004452	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0006288	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0009465	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0011453	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0011454	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:949	Acrocraniofacial dysostosis		HP:0030680	ORPHA:949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0005561	ORPHA:98848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0011121	ORPHA:98848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0031408	ORPHA:98848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0100494	ORPHA:98848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0100495	ORPHA:98848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0000939	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0000988	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0000989	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0001025	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0011354	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0012393	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0025081	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0031284	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0031901	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0032155	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0040186	ORPHA:98848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0100845	ORPHA:98848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0001744	ORPHA:98848	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0002240	ORPHA:98848	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis		HP:0002716	ORPHA:98848	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98848	Indolent systemic mastocytosis	NOT	HP:0004377	ORPHA:98848	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0004377	ORPHA:98849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0012324	ORPHA:98849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0031901	ORPHA:98849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0100494	ORPHA:98849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0000980	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0000989	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001824	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001873	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001880	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001895	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001897	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001945	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001974	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002315	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0005547	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0012378	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0031020	ORPHA:98849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0000939	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001025	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001279	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001649	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0001744	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002014	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002018	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002027	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002086	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002240	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002615	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002653	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002659	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002665	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002716	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002829	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0002863	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0003326	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0004398	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0004808	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0011897	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0012138	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0012325	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0031284	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0031807	ORPHA:98849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0005550	ORPHA:98849	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0006775	ORPHA:98849	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98849	Systemic mastocytosis with associated hematologic neoplasm		HP:0011034	ORPHA:98849	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0000929	ORPHA:945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0007360	ORPHA:945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0001162	ORPHA:945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0001362	ORPHA:945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0002269	ORPHA:945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0000175	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0000238	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0000316	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0001360	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0001539	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0001883	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0002101	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0002414	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:945	Acalvaria		HP:0030680	ORPHA:945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0000820	ORPHA:3143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0000872	ORPHA:3143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0002608	ORPHA:3143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0008207	ORPHA:3143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0100647	ORPHA:3143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0100651	ORPHA:3143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0000135	ORPHA:3143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0000829	ORPHA:3143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0001053	ORPHA:3143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0001596	ORPHA:3143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0003011	ORPHA:3143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3143	Autoimmune polyendocrinopathy type 2		HP:0034061	ORPHA:3143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000028	ORPHA:3144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000175	ORPHA:3144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000256	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000268	ORPHA:3144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000272	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000470	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000773	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000774	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000882	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000895	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000944	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000946	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0000947	ORPHA:3144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0001004	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0001231	ORPHA:3144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0001561	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0001800	ORPHA:3144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0002983	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0003038	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0003312	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0005019	ORPHA:3144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0005616	ORPHA:3144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0008108	ORPHA:3144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0008479	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0008873	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3144	Schneckenbecken dysplasia		HP:0012107	ORPHA:3144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0000010	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0000246	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0000508	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0000819	ORPHA:169105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0001581	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0001618	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0001873	ORPHA:169105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0001881	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0001903	ORPHA:169105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0002014	ORPHA:169105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0002015	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0002094	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0002110	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0002205	ORPHA:169105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0003473	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0004313	ORPHA:169105	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0010515	ORPHA:169105	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0012735	ORPHA:169105	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0100522	ORPHA:169105	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169105	Good syndrome		HP:0100721	ORPHA:169105	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0000347	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0000405	ORPHA:3145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0000494	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0000670	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0000823	ORPHA:3145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0001249	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0001263	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0001376	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0001939	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0002514	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0004322	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0009738	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0009806	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0010669	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3145	Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndrome		HP:0011069	ORPHA:3145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0007185	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0008288	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0011344	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0012444	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0012736	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0100704	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0001942	ORPHA:941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0002448	ORPHA:941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0012379	ORPHA:941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0000252	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0000750	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0001249	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0001250	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0001257	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0001263	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0002154	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0003108	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0008947	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0030781	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0500230	ORPHA:941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0000253	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0000365	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0000729	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0001336	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0002072	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:941	D-glyceric aciduria		HP:0002079	ORPHA:941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0000750	ORPHA:943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001332	ORPHA:943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0012120	ORPHA:943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0034657	ORPHA:943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0000252	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001250	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001263	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001508	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001510	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001638	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001942	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001943	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0011968	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:6000355	ORPHA:943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001252	ORPHA:943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001254	ORPHA:943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0001946	ORPHA:943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0002013	ORPHA:943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:943	Malonic aciduria		HP:0002014	ORPHA:943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0000013	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0000130	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0000137	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0000141	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0000252	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0000924	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0000944	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0001182	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0001367	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0001595	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0002289	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0002815	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0002823	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0002970	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0003019	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0031095	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0003272	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0003307	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0004322	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0005930	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0008724	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0009806	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0011964	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3130	Satoyoshi syndrome		HP:0200102	ORPHA:3130	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0000218	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0001265	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0001288	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0001319	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002093	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003325	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003327	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003557	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003722	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003803	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0009027	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0010628	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0030198	ORPHA:171436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0000275	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0000347	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0000470	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0000508	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0000767	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0000774	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0001349	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0001371	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0001561	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002375	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002515	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002650	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002804	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002827	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002857	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002877	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002970	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003198	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003236	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003306	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003307	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0003798	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0011968	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0030196	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0030200	ORPHA:171436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171436	Typical nemaline myopathy		HP:0002808	ORPHA:171436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0003324	ORPHA:171433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0003798	ORPHA:171433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0006829	ORPHA:171433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0000765	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001265	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001270	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001371	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001558	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001561	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0002015	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0002058	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001288	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0002375	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0002878	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0003202	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0003458	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0003803	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0005855	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0010628	ORPHA:171433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0000316	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0000343	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0000369	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0000602	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001284	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001349	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0001622	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0002705	ORPHA:171433	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy		HP:0002804	ORPHA:171433	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171433	Intermediate nemaline myopathy	NOT	HP:0001638	ORPHA:171433	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000775	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000883	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001181	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001349	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001622	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0002089	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0002804	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0007514	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000765	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001270	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001371	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001558	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001561	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0001623	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0002015	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0002375	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0002878	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0003202	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0003327	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0003798	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0003803	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0005855	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0006829	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0009025	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0010628	ORPHA:171430	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000047	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000054	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000239	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000369	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171430	Severe congenital nemaline myopathy		HP:0000602	ORPHA:171430	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0000044	ORPHA:939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0003128	ORPHA:939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0000325	ORPHA:939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0000343	ORPHA:939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0008551	ORPHA:939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0000252	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0000340	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0000347	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0001250	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0001511	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0002119	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0002120	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0002514	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0007360	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:939	3-hydroxyisobutyric aciduria		HP:0007370	ORPHA:939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000252	ORPHA:3132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0001263	ORPHA:3132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0001999	ORPHA:3132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0005432	ORPHA:3132	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000135	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000218	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000340	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000347	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000400	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000411	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000426	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000444	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000750	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0001363	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0002650	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0002654	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0002987	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0003065	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0004313	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0005001	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0006380	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0012219	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0012490	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0040238	ORPHA:3132	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000028	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000233	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000316	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000358	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000455	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000490	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000510	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000582	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000608	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000648	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000670	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000692	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0000964	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0001007	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0001193	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0001583	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0001772	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0002313	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0002553	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0002827	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0002843	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0003487	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0004315	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0004322	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0005659	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0006895	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0007034	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0007105	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0009553	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0011431	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0011448	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0031008	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3132	Say-Barber-Miller syndrome		HP:0045075	ORPHA:3132	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000023	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000028	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000048	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000051	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000054	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000280	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000286	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000343	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000358	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000465	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000470	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000486	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000494	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000508	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000768	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000879	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0000973	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0001256	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0001363	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0001537	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0001540	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0002162	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0003312	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0001382	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0006297	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0006610	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0008070	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0011084	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0012028	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0012810	ORPHA:3134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0002342	ORPHA:3134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3134	SCARF syndrome		HP:0002557	ORPHA:3134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0000023	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0000767	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0000944	ORPHA:935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0001732	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0001888	ORPHA:935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0001903	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0002024	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0002205	ORPHA:935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0002213	ORPHA:935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0002251	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0003085	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0004349	ORPHA:935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0004422	ORPHA:935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0004430	ORPHA:935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0004432	ORPHA:935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0005374	ORPHA:935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0011364	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:935	Short-limb skeletal dysplasia with severe combined immunodeficiency		HP:0100543	ORPHA:935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0002015	ORPHA:930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0001824	ORPHA:930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0002020	ORPHA:930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0012387	ORPHA:930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0012735	ORPHA:930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0100749	ORPHA:930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0002100	ORPHA:930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0004395	ORPHA:930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0030828	ORPHA:930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:930	Idiopathic achalasia		HP:0031085	ORPHA:930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0000280	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0000365	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0000486	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0000518	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0000618	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0000639	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0000717	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001004	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001249	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001250	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001252	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001257	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001263	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001321	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0001640	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002019	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002020	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002120	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002169	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002321	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002376	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002445	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0002650	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0006532	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0009830	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0010471	ORPHA:3137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0011276	ORPHA:3137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3137	Alpha-N-acetylgalactosaminidase deficiency		HP:0012471	ORPHA:3137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000256	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000343	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000347	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000463	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000470	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000474	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000774	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0001789	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0002007	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0002652	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0002983	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0003196	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0003336	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0003510	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0004348	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0006703	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0010306	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0012368	ORPHA:932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000023	ORPHA:932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0001537	ORPHA:932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0001561	ORPHA:932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0000476	ORPHA:932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:932	Achondrogenesis		HP:0030680	ORPHA:932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0001167	ORPHA:3138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0001231	ORPHA:3138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0002221	ORPHA:3138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0004370	ORPHA:3138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0006495	ORPHA:3138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000028	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000130	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000144	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000823	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0001513	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0002557	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0003019	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0004322	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0008736	ORPHA:3138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000089	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000668	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000768	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000889	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0000912	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0001162	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0001601	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0001629	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0001800	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0002021	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0002023	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0002818	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0031095	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0004050	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0004299	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0004397	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0005916	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0009751	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0009882	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0011675	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0100490	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3138	Ulnar-mammary syndrome		HP:0100783	ORPHA:3138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0000944	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0002990	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0003974	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0003982	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0004050	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0005792	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0005930	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:931	Isolated acheiropodia		HP:0009813	ORPHA:931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0000975	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0001182	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0001810	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0001842	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0002645	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0002797	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0002815	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0003028	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0003103	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0003202	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0003272	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0003307	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0004349	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0005930	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:970	Hereditary sensory and autonomic neuropathy type 2		HP:0008391	ORPHA:970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0000776	ORPHA:972	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0001250	ORPHA:972	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0001251	ORPHA:972	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0001260	ORPHA:972	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0001350	ORPHA:972	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0002064	ORPHA:972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0003236	ORPHA:972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0003457	ORPHA:972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0003803	ORPHA:972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:972	Hereditary continuous muscle fiber activity		HP:0100022	ORPHA:972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0001171	ORPHA:971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0008678	ORPHA:971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0012210	ORPHA:971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0000083	ORPHA:971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0002992	ORPHA:971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0006501	ORPHA:971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0040071	ORPHA:971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0000175	ORPHA:971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0000347	ORPHA:971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0000478	ORPHA:971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:971	Acrorenal syndrome		HP:0000504	ORPHA:971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0001876	ORPHA:86843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0011974	ORPHA:86843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0001324	ORPHA:86843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0012129	ORPHA:86843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0012143	ORPHA:86843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0012378	ORPHA:86843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0031020	ORPHA:86843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0003419	ORPHA:86843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0004808	ORPHA:86843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0004820	ORPHA:86843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0005528	ORPHA:86843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0031385	ORPHA:86843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0031386	ORPHA:86843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0100827	ORPHA:86843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86843	Acute panmyelosis with myelofibrosis		HP:0001744	ORPHA:86843	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0002863	ORPHA:86841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0001877	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0001894	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0001972	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0012133	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0012143	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0025435	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0031020	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0031385	ORPHA:86841	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0001882	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0001892	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0004808	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0005528	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0011273	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0011992	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0012129	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0012148	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86841	Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality		HP:0031035	ORPHA:86841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0010896	ORPHA:3129	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0010897	ORPHA:3129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0000486	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0000648	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0000712	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0001251	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0001256	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0001263	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0001270	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0001639	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0001642	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0002069	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0002273	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0002360	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0002371	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0002465	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0007875	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0008610	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0008947	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0010522	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0011727	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3129	Sarcosinemia		HP:0100022	ORPHA:3129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0002863	ORPHA:98826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0010972	ORPHA:98826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0001972	ORPHA:98826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0012133	ORPHA:98826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0012150	ORPHA:98826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0012378	ORPHA:98826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0001895	ORPHA:98826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0001897	ORPHA:98826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0002094	ORPHA:98826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0005528	ORPHA:98826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0030872	ORPHA:98826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0001873	ORPHA:98826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0001875	ORPHA:98826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98826	Myelodysplastic neoplasm with low blasts		HP:0001892	ORPHA:98826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0002863	ORPHA:98827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0001871	ORPHA:98827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0012148	ORPHA:98827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0012378	ORPHA:98827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0045040	ORPHA:98827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0001974	ORPHA:98827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0002960	ORPHA:98827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0005528	ORPHA:98827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0030166	ORPHA:98827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98827	Unclassified myelodysplastic syndrome		HP:0004808	ORPHA:98827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000023	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000028	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000160	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000233	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000252	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000348	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000444	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000494	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000508	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000512	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000649	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000678	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000768	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000774	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000790	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0000823	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0001053	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0001156	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0001249	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0001250	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0001263	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0001511	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0002230	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0002650	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0002808	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0002983	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0003196	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0004209	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0005048	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0009623	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0009811	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0010049	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0010579	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0100542	ORPHA:3121	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0100734	ORPHA:3121	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3121	Ruvalcaba syndrome		HP:0200055	ORPHA:3121	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000160	ORPHA:969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000179	ORPHA:969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000311	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000343	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000414	ORPHA:969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000463	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000527	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000534	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0000762	ORPHA:969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0001156	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0001387	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0001609	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0002750	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0002823	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0003196	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0003300	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0003510	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0004279	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0005900	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0005930	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0010049	ORPHA:969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:969	Acromicric dysplasia		HP:0200055	ORPHA:969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0001156	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0001387	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002167	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002644	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002650	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002827	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0002999	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0003028	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0003042	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0003086	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0006011	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0006014	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0007598	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0008368	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0008890	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0009778	ORPHA:968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0010049	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:968	Acromesomelic dysplasia, Hunter-Thompson type		HP:0100543	ORPHA:968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0002161	ORPHA:3124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0011021	ORPHA:3124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0001507	ORPHA:3124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0003297	ORPHA:3124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0004322	ORPHA:3124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0001250	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0001256	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0001264	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0001268	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0001337	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0001987	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0002066	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0002936	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0003131	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0011966	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0012758	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0032397	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0100543	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3124	Saccharopinuria		HP:0500151	ORPHA:3124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001869	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002758	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002829	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0003859	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0004099	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0006191	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000158	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000276	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000280	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000293	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000303	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000337	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000400	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000445	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000818	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000830	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000845	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000975	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001051	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001072	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001176	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001182	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001386	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001769	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0011760	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0011334	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0012185	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0012471	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0012802	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0025406	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0025693	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0030269	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0100540	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0100607	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000238	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000602	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000689	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000789	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000802	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000846	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000869	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000876	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000956	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000998	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001061	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001081	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001123	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001639	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001653	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002155	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002315	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002953	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0003233	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0003326	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0005266	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0006767	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0006824	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0007440	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0008245	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0010541	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0011675	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0012452	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0030166	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0012378	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0033794	ORPHA:963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000044	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000164	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000336	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000664	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000687	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000716	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000739	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000819	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000822	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000855	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0000870	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0001609	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002007	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002076	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002230	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0002808	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0003401	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0003416	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0005978	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0005987	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0010535	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0010609	ORPHA:963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0031653	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0046504	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0100518	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0100786	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:963	Acromegaly		HP:0100829	ORPHA:963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0007359	ORPHA:98820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0011185	ORPHA:98820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0002069	ORPHA:98820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0025373	ORPHA:98820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0031951	ORPHA:98820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0000708	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0000729	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0000980	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0001249	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0002349	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0002367	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0002384	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0002427	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0003401	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0008765	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0010841	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0012005	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0012469	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0012531	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0031284	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0032046	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0100543	ORPHA:98820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0002126	ORPHA:98820	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0002521	ORPHA:98820	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0007206	ORPHA:98820	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98820	Familial focal epilepsy with variable foci		HP:0011171	ORPHA:98820	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0001250	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0001276	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0001336	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0001561	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0001999	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0002365	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0002804	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0002871	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0004887	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0006955	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0011451	ORPHA:166063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0000340	ORPHA:166063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0000347	ORPHA:166063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166063	Pontocerebellar hypoplasia type 4		HP:0011800	ORPHA:166063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0000520	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0000929	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0001274	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0001360	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0001561	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0002683	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0005466	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0007360	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0012443	ORPHA:563612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0000369	ORPHA:563612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0005280	ORPHA:563612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0009800	ORPHA:563612	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0010627	ORPHA:563612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0011756	ORPHA:563612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0011821	ORPHA:563612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563612	Isolated exencephaly		HP:0030244	ORPHA:563612	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0010972	ORPHA:86839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0012378	ORPHA:86839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0001017	ORPHA:86839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0001945	ORPHA:86839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0001962	ORPHA:86839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0002875	ORPHA:86839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0000573	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0001873	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0001892	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0001974	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0002653	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0004808	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0005528	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0005561	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0010741	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0010876	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0012116	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0012136	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0012148	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0012150	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0025065	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86839	Myelodysplastic neoplasm with increased blasts		HP:0031035	ORPHA:86839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000407	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001251	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001263	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001270	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001738	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001999	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0002342	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0003693	ORPHA:456312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000219	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000248	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000309	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000577	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000819	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001155	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001310	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001319	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001508	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001530	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001760	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001771	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0002353	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0002460	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0005484	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0009623	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0010628	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0100307	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0100807	ORPHA:456312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000049	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000316	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000821	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0000823	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001374	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001558	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001772	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0001844	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0002123	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0002240	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0003431	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0003448	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0006276	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0008366	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0009463	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0009464	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0009473	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0012418	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0030146	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0030951	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		HP:0100800	ORPHA:456312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000085	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0001172	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0002818	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0004712	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0004736	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0006501	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0009650	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0009778	ORPHA:959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000015	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000405	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000407	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000486	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000505	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000588	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0001177	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0001199	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0001852	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0003022	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0006433	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0007766	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0008678	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0010059	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0010109	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0012745	ORPHA:959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000076	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000286	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000316	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000482	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000508	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000518	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000567	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000568	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000589	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000612	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0000639	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0001636	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0001770	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0001883	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0002251	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0002948	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0003422	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0005792	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0006101	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:959	Acro-renal-ocular syndrome		HP:0008897	ORPHA:959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0001250	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002371	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002381	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002463	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0011098	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0025373	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0030391	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0031491	ORPHA:98818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000708	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000729	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002121	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002376	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0007018	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0007086	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0009088	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0011153	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0011198	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0012015	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0012018	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0025190	ORPHA:98818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000712	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000716	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000718	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000736	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000739	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0000752	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0001350	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002066	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002069	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002300	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002354	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002359	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002360	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0002384	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0003376	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0003698	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0007270	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0011166	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0011169	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0031951	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0032671	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0100710	ORPHA:98818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0030057	ORPHA:98818	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98818	Landau-Kleffner syndrome		HP:0200134	ORPHA:98818	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001266	ORPHA:98811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001332	ORPHA:98811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0007166	ORPHA:98811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001249	ORPHA:98811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001250	ORPHA:98811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001304	ORPHA:98811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0002121	ORPHA:98811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0003401	ORPHA:98811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0004305	ORPHA:98811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0006801	ORPHA:98811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0000718	ORPHA:98811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0000737	ORPHA:98811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001251	ORPHA:98811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001328	ORPHA:98811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0002072	ORPHA:98811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0001256	ORPHA:98811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98811	Paroxysmal exertion-induced dyskinesia		HP:0002061	ORPHA:98811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000316	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000343	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000347	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000494	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000574	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000704	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000929	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000938	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000939	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001156	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001831	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001999	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002652	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002797	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0004322	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0004331	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0009882	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0011305	ORPHA:955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000160	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000164	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000233	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000256	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000268	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000269	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000277	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000280	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000293	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000365	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000445	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000463	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000470	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000506	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001231	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002230	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002308	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002645	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002650	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002653	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002688	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002691	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002714	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002757	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002829	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0004586	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001382	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0008424	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0010807	ORPHA:955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000023	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000047	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000175	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000238	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000294	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000369	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000431	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000518	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000545	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000612	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000664	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000768	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000823	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0000958	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001072	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001508	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001537	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001608	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001629	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001643	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001650	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001718	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0001744	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002205	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002208	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002240	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002315	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002566	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002808	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0002999	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0003396	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0005562	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0006487	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0009830	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0010669	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0030680	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0100670	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0100790	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:955	Hajdu-Cheney syndrome		HP:0200042	ORPHA:955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0000952	ORPHA:3111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0002908	ORPHA:3111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0012379	ORPHA:3111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0002904	ORPHA:3111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0010473	ORPHA:3111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0031811	ORPHA:3111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0001046	ORPHA:3111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome		HP:0032106	ORPHA:3111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome	NOT	HP:0000989	ORPHA:3111	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3111	Rotor syndrome	NOT	HP:0031137	ORPHA:3111	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000202	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000218	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000275	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000322	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000347	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000358	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000470	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000494	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000768	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000776	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000813	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000882	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000883	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000889	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0000912	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0001171	ORPHA:958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0001511	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0001562	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0001839	ORPHA:958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002089	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002101	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002575	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002650	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002808	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002827	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002937	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0002984	ORPHA:958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0003022	ORPHA:958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0003316	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0003762	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0004408	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0006101	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0006381	ORPHA:958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0006426	ORPHA:958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0008678	ORPHA:958	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0010295	ORPHA:958	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:958	Acro-renal-mandibular syndrome		HP:0010669	ORPHA:958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0000698	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0000966	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0000968	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0001508	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0001510	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0002718	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0008070	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0010701	ORPHA:98813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0000403	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0002028	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0002037	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0002728	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0005404	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0011274	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0033581	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0100828	ORPHA:98813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0000938	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0000964	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0002720	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0002850	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0002960	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0003212	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0003237	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0003496	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0004313	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0004315	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0008404	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0008872	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0010741	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0011108	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0020101	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0031188	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0031691	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98813	Hypohidrotic ectodermal dysplasia with immunodeficiency		HP:0040075	ORPHA:98813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0000175	ORPHA:957	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0000767	ORPHA:957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0001199	ORPHA:957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0001256	ORPHA:957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0002414	ORPHA:957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0002705	ORPHA:957	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0005048	ORPHA:957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0006101	ORPHA:957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0008368	ORPHA:957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0009882	ORPHA:957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0011304	ORPHA:957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:957	Acropectorovertebral dysplasia		HP:0100490	ORPHA:957	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0000164	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0000190	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0000668	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0000698	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0001162	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0001231	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0001792	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0001800	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0002006	ORPHA:952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0003502	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0004209	ORPHA:952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0006288	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0006315	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0008388	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0008404	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0009738	ORPHA:952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0010557	ORPHA:952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0100797	ORPHA:952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:952	Acrofacial dysostosis, Weyers type		HP:0200055	ORPHA:952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0000639	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0001284	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0001761	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0001762	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002066	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002070	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002174	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002312	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002317	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0001288	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002495	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002650	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002751	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0003431	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0003474	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0003693	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0007131	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0007141	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0007328	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0007340	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0010829	ORPHA:3115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002359	ORPHA:3115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002839	ORPHA:3115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0002857	ORPHA:3115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0003202	ORPHA:3115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0003487	ORPHA:3115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3115	Roussy-Lévy syndrome		HP:0008954	ORPHA:3115	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0000835	ORPHA:563609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0001511	ORPHA:563609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0000776	ORPHA:563609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0001539	ORPHA:563609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0009800	ORPHA:563609	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0010516	ORPHA:563609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0030244	ORPHA:563609	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:563609	Isolated anencephaly		HP:0410030	ORPHA:563609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0001332	ORPHA:98810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0007166	ORPHA:98810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0001266	ORPHA:98810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0002072	ORPHA:98810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0002487	ORPHA:98810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0004305	ORPHA:98810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0000211	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0000473	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0001387	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0002063	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0002094	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0002167	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0003324	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0025401	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98810	Paroxysmal non-kinesigenic dyskinesia		HP:0100660	ORPHA:98810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000099	ORPHA:93126	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000083	ORPHA:93126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000093	ORPHA:93126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0002907	ORPHA:93126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0003259	ORPHA:93126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0011944	ORPHA:93126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0012213	ORPHA:93126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0032230	ORPHA:93126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000096	ORPHA:93126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000951	ORPHA:93126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0001945	ORPHA:93126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0002086	ORPHA:93126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0008653	ORPHA:93126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000478	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000979	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0001609	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0001919	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0001970	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0002027	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0002087	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0002094	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0002829	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0003493	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0004930	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0012089	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0012587	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0012593	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0012735	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0040223	ORPHA:93126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0000155	ORPHA:93126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0001626	ORPHA:93126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0001733	ORPHA:93126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0011024	ORPHA:93126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0032018	ORPHA:93126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis		HP:0100532	ORPHA:93126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis	NOT	HP:0002955	ORPHA:93126	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93126	Pauci-immune glomerulonephritis	NOT	HP:0032616	ORPHA:93126	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0001892	ORPHA:98892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0002020	ORPHA:98892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0002021	ORPHA:98892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0002650	ORPHA:98892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0100790	ORPHA:98892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0000963	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0001382	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0001643	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0001654	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0001659	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0007165	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0007359	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0012639	ORPHA:98892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0002999	ORPHA:98892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0003834	ORPHA:98892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98892	Periventricular nodular heterotopia		HP:0004942	ORPHA:98892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000282	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001873	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001945	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002014	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002315	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002910	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0003326	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0025258	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0025439	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0031691	ORPHA:319213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000083	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000707	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000988	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001259	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001289	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001882	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001888	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001942	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001974	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002013	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002018	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002907	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0003645	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0007430	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0011227	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0011896	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0025435	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0031273	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0031364	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0040186	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0100520	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0100749	ORPHA:319213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000613	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000739	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000975	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0000979	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001250	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001268	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001324	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0001662	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002015	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002069	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002098	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002181	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002322	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002329	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0002615	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0004787	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0009830	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0012384	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0012819	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0025145	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0030139	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0030830	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0031246	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0032043	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0032155	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0100539	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319213	Lujo hemorrhagic fever		HP:0100750	ORPHA:319213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000127	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000841	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000848	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000859	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001960	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0002900	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0004727	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0008619	ORPHA:89938	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001252	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001270	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001324	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001508	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001518	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001561	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001622	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0002150	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0002902	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0002917	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0003081	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0003113	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0003527	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0012622	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0025335	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0031936	ORPHA:89938	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000121	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000712	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001525	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001919	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0001944	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0002013	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0002312	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0003774	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0040288	ORPHA:89938	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000325	ORPHA:89938	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4		HP:0000411	ORPHA:89938	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:89938	Bartter syndrome type 4	NOT	HP:0000822	ORPHA:89938	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000529	ORPHA:98890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000543	ORPHA:98890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000551	ORPHA:98890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000603	ORPHA:98890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000648	ORPHA:98890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0007663	ORPHA:98890	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000639	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000712	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0000762	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0001249	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0001266	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0002066	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0002075	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0002080	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0003487	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0012164	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98890	Early-onset X-linked optic atrophy		HP:0012638	ORPHA:98890	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97560	Primary membranous glomerulonephritis		HP:0034002	ORPHA:97560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0006487	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0008117	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0008144	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0010299	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0025335	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0030757	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0031936	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000360	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000787	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000867	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000920	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0006640	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0001324	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0001363	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0001369	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0001376	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002007	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002015	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002176	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002360	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002869	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0003416	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0006432	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0007099	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0008442	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0012378	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0012449	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0025369	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0100686	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:6000407	ORPHA:89936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000407	ORPHA:89936	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0005789	ORPHA:89936	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0100658	ORPHA:89936	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000117	ORPHA:89936	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002148	ORPHA:89936	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002748	ORPHA:89936	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0003127	ORPHA:89936	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0003155	ORPHA:89936	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0006490	ORPHA:89936	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000121	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000694	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0000897	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0001510	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002653	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002829	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002857	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002970	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0002979	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0003498	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0003856	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0004349	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89936	X-linked hypophosphatemia		HP:0005930	ORPHA:89936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0002148	ORPHA:89937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0003109	ORPHA:89937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0001324	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0001510	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0001891	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0002653	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0002748	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0002749	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0002979	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0003155	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0012378	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0030757	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0100512	ORPHA:89937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0020110	ORPHA:89937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:89937	Autosomal dominant hypophosphatemic rickets		HP:0002901	ORPHA:89937	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000316	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000431	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000445	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000463	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0001156	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002983	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0003196	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0004279	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0008736	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0011800	ORPHA:3107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000028	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000059	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000060	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000064	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000168	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000212	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000256	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000278	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000286	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000343	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000347	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000520	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000527	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000582	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000637	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000767	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0001537	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002007	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002705	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002714	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002937	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0003312	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0003510	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0004209	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0004322	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0005280	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0007665	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0009099	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0010297	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0010807	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0011220	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0012905	ORPHA:3107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000023	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000036	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000039	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000047	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000322	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000358	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000365	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000369	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000470	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000486	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000494	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000508	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000592	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000668	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000674	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000677	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000768	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0000960	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0001249	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0001263	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0001328	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0001385	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0001596	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002650	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002673	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002812	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0002827	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0003042	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0005306	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0005743	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0006101	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0008402	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0010733	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0011069	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0040036	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0100490	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0100541	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3107	Autosomal dominant Robinow syndrome		HP:0100798	ORPHA:3107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000505	ORPHA:909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001118	ORPHA:909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0012379	ORPHA:909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000543	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000639	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000649	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000708	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000762	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000939	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001138	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001167	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001249	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001250	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001251	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001257	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001260	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001288	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001317	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001328	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001332	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001347	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001761	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002028	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002071	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002310	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002385	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002453	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002992	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0003487	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0003693	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0005109	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0006958	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0007256	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0007272	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0007377	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0008046	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0009830	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0010874	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0011931	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0012758	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0012896	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0030890	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0100543	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0100872	ORPHA:909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000464	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000492	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000520	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000648	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000713	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000716	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000717	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000718	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000736	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000738	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000821	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0000938	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001081	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001155	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001272	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0001300	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002151	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002171	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002283	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002322	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002423	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002659	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002823	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002942	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0004416	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0005181	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0006480	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0006579	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0007018	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0007305	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0007495	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0007922	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0008516	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0009811	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0011994	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0012075	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0012706	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0012707	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0031589	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0040078	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0100321	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0200125	ORPHA:909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002088	ORPHA:909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002196	ORPHA:909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0002313	ORPHA:909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0003474	ORPHA:909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:909	Cerebrotendinous xanthomatosis		HP:0010530	ORPHA:909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000053	ORPHA:908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000389	ORPHA:908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0001382	ORPHA:908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0001763	ORPHA:908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002167	ORPHA:908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002342	ORPHA:908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0003564	ORPHA:908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000246	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000256	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000275	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000276	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000303	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000388	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000400	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000411	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000750	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0001252	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002003	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002007	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002020	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002194	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002360	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002650	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0007018	ORPHA:908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000486	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000717	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000737	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0000739	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0001250	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0001634	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0002120	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0004970	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:908	Fragile X syndrome		HP:0100716	ORPHA:908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0000365	ORPHA:3109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0001631	ORPHA:3109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0001642	ORPHA:3109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0000151	ORPHA:3109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0000786	ORPHA:3109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0008726	ORPHA:3109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0000077	ORPHA:3109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0002027	ORPHA:3109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0030016	ORPHA:3109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0000085	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0000086	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0000122	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0002948	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0003312	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0003422	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0005107	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0010463	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0030127	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0031086	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3109	Mayer-Rokitansky-Küster-Hauser syndrome		HP:0031703	ORPHA:3109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000140	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000716	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000718	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000952	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000978	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000989	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001155	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001249	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001260	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001369	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001386	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001394	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001397	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001508	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001744	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001824	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001873	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001903	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002240	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002312	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001288	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002653	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002756	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002829	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002910	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0003418	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0004324	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0006554	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0008994	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0012115	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:5200321	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0200032	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0200119	ORPHA:905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000751	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000939	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001288	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001332	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001337	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001878	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002072	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0010837	ORPHA:905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000709	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000738	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000739	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000787	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000789	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0000829	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001250	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001541	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0001733	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002013	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0002027	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0003355	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0003781	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0012748	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:0100785	ORPHA:905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:905	Wilson disease		HP:6000642	ORPHA:905	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001263	ORPHA:480880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002342	ORPHA:480880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000119	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000453	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000478	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001305	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002023	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002079	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002536	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0004322	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0007483	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0008947	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0100259	ORPHA:480880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000110	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000126	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000164	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000175	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000212	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000218	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000219	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000248	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000324	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000341	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000343	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000365	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000358	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000369	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000431	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000448	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000454	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000483	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000486	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000494	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000506	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000518	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000540	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000545	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000582	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000692	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000823	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000938	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000960	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0000998	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001182	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001238	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001250	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001320	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001321	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001374	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001376	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001385	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001382	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001631	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001638	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001643	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001761	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001763	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001773	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001822	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001845	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002098	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002119	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002198	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002212	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0001288	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002365	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002557	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002650	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002664	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0002944	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0004095	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0004298	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0005272	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0005280	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0005722	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0007360	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0010499	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0011220	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0011968	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0012444	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0012471	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0012745	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0012810	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0030925	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0030928	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0031508	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0100890	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0200055	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0200117	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability		HP:0410026	ORPHA:480880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000010	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000014	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000015	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000023	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000025	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000028	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000044	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000075	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000076	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000083	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000089	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000093	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000121	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000125	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000147	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000154	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000158	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000179	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000212	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000232	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000252	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000275	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000280	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000286	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000307	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000337	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000343	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000347	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000348	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000358	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000389	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000400	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000407	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000411	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000431	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000464	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000485	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000486	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000501	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000505	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000518	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000545	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000581	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000627	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000632	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000635	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000668	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000670	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000682	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000689	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000691	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000716	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000717	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000722	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000739	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000767	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000787	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000821	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000822	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000826	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000938	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000939	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0000960	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001052	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001081	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001136	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001181	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001231	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001249	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001251	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001252	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001257	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001260	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001288	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001297	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001310	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001337	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001347	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001361	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001387	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001382	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001513	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001531	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001537	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001582	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001608	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001609	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001618	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001626	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001629	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001631	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001634	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001635	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001636	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001639	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001640	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001642	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001643	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001645	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001647	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001653	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001658	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001671	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001763	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001800	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001822	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001969	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002017	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002019	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002020	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002024	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002027	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002035	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002071	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002120	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002141	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002150	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002167	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002183	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002205	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002253	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002308	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002376	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002575	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002623	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002637	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002644	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002650	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002750	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002808	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002829	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002857	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002974	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0002999	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003028	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003072	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003119	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003196	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003198	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003236	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003298	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003307	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003312	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0003422	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004209	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004295	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004305	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004306	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004322	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004381	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004398	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004428	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0004969	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0005113	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0005344	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0005562	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0001382	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0005978	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0006482	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0007018	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0007372	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0007477	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0007495	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0007720	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0007957	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0008053	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0008499	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0008661	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0008736	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0010526	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0010662	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0010669	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0010780	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0010807	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0010880	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0011001	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0012433	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0012639	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100025	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100240	ORPHA:904	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100539	ORPHA:904	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100545	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100613	ORPHA:904	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100659	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100785	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0100817	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:904	Williams syndrome		HP:0200021	ORPHA:904	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0000238	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0000648	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0001321	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0002085	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0002282	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0002365	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0002500	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0007260	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0011344	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0012447	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0032398	ORPHA:352682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement		HP:0001250	ORPHA:352682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement	NOT	HP:0003457	ORPHA:352682	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000112	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000140	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000225	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000246	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000388	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000389	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000421	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000491	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000498	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000509	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000778	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000964	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000967	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000978	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0000979	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001025	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001287	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001328	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001369	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001645	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001873	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001875	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001878	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001879	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001888	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001903	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001935	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0001945	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002028	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002037	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002094	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002170	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002205	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002248	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002488	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002573	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002633	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002664	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002665	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002721	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0002960	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0003010	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0005558	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0006510	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0006535	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0007420	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0009830	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0011029	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0011675	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0011869	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0011875	ORPHA:906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0012378	ORPHA:906	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0100749	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0100774	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0100806	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0100820	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:906	Wiskott-Aldrich syndrome		HP:0200042	ORPHA:906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0000989	ORPHA:901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0100658	ORPHA:901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0000969	ORPHA:901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0001880	ORPHA:901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0008066	ORPHA:901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0200037	ORPHA:901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0001945	ORPHA:901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome		HP:0002829	ORPHA:901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:901	Wells syndrome	NOT	HP:0002633	ORPHA:901	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0000640	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0000716	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0000739	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0001260	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0001618	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002019	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002066	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002068	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002070	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002073	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002136	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002172	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002174	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002310	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002359	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002494	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002530	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0004926	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0005341	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0007256	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0008652	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0010307	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0010536	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0010545	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0012332	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0012658	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0012670	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0030015	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0030880	ORPHA:227510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0000741	ORPHA:227510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0001300	ORPHA:227510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002063	ORPHA:227510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002067	ORPHA:227510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0002322	ORPHA:227510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227510	Multiple system atrophy, cerebellar type		HP:0100595	ORPHA:227510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000163	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000246	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000366	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000388	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000421	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000790	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001824	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001945	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002113	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002205	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002633	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002637	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002829	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002955	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002960	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0012378	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0100820	ORPHA:900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000093	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000099	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000579	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000864	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000988	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001369	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002017	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002027	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002093	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002105	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002206	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0003565	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0005764	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0006510	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0006535	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0009830	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0011227	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0012649	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0012735	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0032230	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0033557	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0033559	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0034104	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0100532	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0100533	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0100539	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0100749	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0200034	ORPHA:900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000024	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000071	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000083	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000126	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000389	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000407	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000488	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000491	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000505	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000520	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000763	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000822	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000873	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0000979	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001250	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001287	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001607	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001681	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001701	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0001733	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002091	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002102	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002202	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002239	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002301	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0002315	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0003326	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0004936	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0005214	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0006824	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0011675	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0025420	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0033608	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0100758	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:900	Granulomatosis with polyangiitis		HP:0200042	ORPHA:900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002269	ORPHA:98889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0032407	ORPHA:98889	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0000750	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001249	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001250	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001257	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001263	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001328	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001347	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001371	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002392	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002463	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0005684	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0007359	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0008947	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0012014	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0012017	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0020190	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0030319	ORPHA:98889	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0000252	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0000347	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0000365	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0000453	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0000639	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0000767	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001260	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001310	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001320	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001349	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0001511	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002015	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002020	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002061	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002104	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002307	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002385	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002509	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002510	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0002835	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0007024	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0007033	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0007301	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0010808	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0011157	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0011755	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0011968	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0012015	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0012469	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98889	Bilateral perisylvian polymicrogyria		HP:0410011	ORPHA:98889	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0001872	ORPHA:903	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0001928	ORPHA:903	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0008330	ORPHA:903	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0011869	ORPHA:903	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0000132	ORPHA:903	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0000421	ORPHA:903	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0000471	ORPHA:903	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0000978	ORPHA:903	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0001633	ORPHA:903	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0003125	ORPHA:903	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0030129	ORPHA:903	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0000967	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0001873	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0001935	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0002239	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0003645	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0004097	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0005261	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0005293	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:903	Von Willebrand disease		HP:0040242	ORPHA:903	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0000768	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0002187	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0002751	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0004322	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0006462	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0011964	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0012899	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0012903	ORPHA:3101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0001621	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0002015	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0002527	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0003712	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0005638	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0008422	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0009053	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0100288	ORPHA:3101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0000565	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0001265	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0001284	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0001840	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0002540	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0002857	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0003199	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0004568	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome		HP:0007156	ORPHA:3101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0000160	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0000164	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0000294	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0000369	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0000470	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0000581	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0001373	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0001376	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0001540	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0001620	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3101	Richieri Costa-da Silva syndrome	NOT	HP:0012368	ORPHA:3101	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000135	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000444	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000518	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000765	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000939	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0001533	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0001608	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002209	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002211	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002216	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0003777	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0004322	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0007495	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0010721	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100578	ORPHA:902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000035	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000144	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000275	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000855	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000934	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000962	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0001635	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0001658	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0001838	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002621	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0003202	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0004415	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0005978	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0007618	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0007703	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0008065	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0009125	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0010468	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0011001	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100585	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100679	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0200042	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0200055	ORPHA:902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000822	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0000869	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0001387	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0001601	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002664	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002672	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002858	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002860	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002861	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0002890	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0003002	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0005268	ORPHA:902	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0009726	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0012056	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0012060	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100242	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100526	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100615	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100649	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100659	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:902	Werner syndrome		HP:0100833	ORPHA:902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0000308	ORPHA:3102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0000377	ORPHA:3102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0001762	ORPHA:3102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0006355	ORPHA:3102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0009601	ORPHA:3102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0010109	ORPHA:3102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0000201	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0000690	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0001245	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0001609	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0002643	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0002984	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0003038	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0004209	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0004322	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0004987	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0005011	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0005736	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0006536	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0008872	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0009237	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0010752	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0012789	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0200154	ORPHA:3102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0000193	ORPHA:3102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0001328	ORPHA:3102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0008744	ORPHA:3102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0010565	ORPHA:3102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3102	Richieri Costa-Pereira syndrome		HP:0011051	ORPHA:3102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000248	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000252	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000272	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000316	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000430	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0002817	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0002984	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0004209	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0005011	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0006487	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0008070	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0008846	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0008897	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0009466	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0009601	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0009623	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0009829	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0009943	ORPHA:3103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000028	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000040	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000175	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000204	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000347	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000387	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000518	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000520	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001156	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001249	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001263	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001622	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0002974	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0007452	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000377	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0008665	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0009891	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0030680	ORPHA:3103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000113	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000218	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000470	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000501	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000568	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000592	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0000639	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001239	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001363	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001561	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001852	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0001873	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0005048	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0005876	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0006101	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0006380	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0006443	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3103	Roberts syndrome		HP:0007598	ORPHA:3103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0001347	ORPHA:59298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002315	ORPHA:59298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002344	ORPHA:59298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002922	ORPHA:59298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0007305	ORPHA:59298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0030890	ORPHA:59298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0000565	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0000651	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0001250	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0001251	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0001298	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0001324	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002013	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002018	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002172	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002321	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0002516	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0011448	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59298	Schilder disease		HP:0012229	ORPHA:59298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0000162	ORPHA:3104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0000347	ORPHA:3104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0009380	ORPHA:3104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0040071	ORPHA:3104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0000164	ORPHA:3104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0000175	ORPHA:3104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0000275	ORPHA:3104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0004209	ORPHA:3104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0005916	ORPHA:3104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3104	Robin sequence-oligodactyly syndrome		HP:0003312	ORPHA:3104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0001945	ORPHA:319218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002014	ORPHA:319218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0010702	ORPHA:319218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0020071	ORPHA:319218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0100749	ORPHA:319218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0001882	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0001888	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0001892	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002013	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002015	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002018	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002027	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002239	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002249	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002315	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0004396	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0012115	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0012735	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0025143	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0025439	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0040186	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0100806	ORPHA:319218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0001254	ORPHA:319218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0001735	ORPHA:319218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0001873	ORPHA:319218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002094	ORPHA:319218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0002829	ORPHA:319218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0005521	ORPHA:319218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319218	Ebola hemorrhagic fever		HP:0100247	ORPHA:319218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98880	Familial afibrinogenemia		HP:0000225	ORPHA:98880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98880	Familial afibrinogenemia		HP:0000421	ORPHA:98880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98880	Familial afibrinogenemia		HP:0001342	ORPHA:98880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98880	Familial afibrinogenemia		HP:0001386	ORPHA:98880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98880	Familial afibrinogenemia		HP:0001892	ORPHA:98880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98880	Familial afibrinogenemia		HP:0005268	ORPHA:98880	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:98880	Familial afibrinogenemia		HP:0400008	ORPHA:98880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98881	Familial dysfibrinogenemia		HP:0000225	ORPHA:98881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98881	Familial dysfibrinogenemia		HP:0000421	ORPHA:98881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98881	Familial dysfibrinogenemia		HP:0001892	ORPHA:98881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98881	Familial dysfibrinogenemia		HP:0002239	ORPHA:98881	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98881	Familial dysfibrinogenemia		HP:0004936	ORPHA:98881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0002719	ORPHA:169154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001508	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001888	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0004429	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0005403	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0032218	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0005415	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0031381	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0045080	ORPHA:169154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0000155	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001019	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001433	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001596	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001875	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001880	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001945	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0001973	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0002028	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0002716	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0002783	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0002788	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0003212	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0003237	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0003261	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0005401	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0010702	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0025526	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0040187	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169154	T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency		HP:0100827	ORPHA:169154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001324	ORPHA:300605	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002061	ORPHA:300605	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0003202	ORPHA:300605	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0003693	ORPHA:300605	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0006986	ORPHA:300605	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0007354	ORPHA:300605	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001264	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001276	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001332	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001348	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002167	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001288	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002460	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002483	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002540	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0003429	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0005750	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0031936	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0031960	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0100295	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0100360	ORPHA:300605	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0000020	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0000252	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0000605	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0000639	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0000708	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001251	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001263	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001300	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0001317	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002015	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002072	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002169	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002179	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002425	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002530	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002544	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002599	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0002650	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0003701	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0003722	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0004326	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0011471	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0012048	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0030051	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300605	Juvenile amyotrophic lateral sclerosis		HP:0100543	ORPHA:300605	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000175	ORPHA:1393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000347	ORPHA:1393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0001591	ORPHA:1393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002643	ORPHA:1393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0030282	ORPHA:1393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000162	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000405	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000413	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0001249	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0001511	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0001522	ORPHA:1393	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002779	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002808	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0004322	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0011968	ORPHA:1393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000003	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000252	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0000465	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0001629	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002132	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002324	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002414	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002435	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002475	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0002514	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0004209	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1393	Cerebrocostomandibular syndrome		HP:0010290	ORPHA:1393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0002372	ORPHA:31709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0001250	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0001266	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0001332	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0002072	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0002305	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0002384	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0004305	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0007166	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0007359	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0032755	ORPHA:31709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0011172	ORPHA:31709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis		HP:0012002	ORPHA:31709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31709	Infantile convulsions and choreoathetosis	NOT	HP:0410263	ORPHA:31709	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000174	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000272	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000278	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000286	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000366	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000358	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000494	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000508	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000512	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000545	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000662	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000664	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0000670	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0001100	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0001156	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0001276	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0002650	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0004209	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0001382	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0007703	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0008046	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0100543	ORPHA:1390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1390	Night blindness-skeletal anomalies-dysmorphism syndrome		HP:0200021	ORPHA:1390	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001324	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001508	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001639	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001640	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001712	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0002240	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0003236	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0008872	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0008947	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0010471	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0012379	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0025335	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0025336	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0025435	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0031964	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0032092	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0040329	ORPHA:308552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0000158	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0000183	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0000297	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001270	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001284	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0002093	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0002098	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0002747	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0002878	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0003324	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0003701	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0004887	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0005165	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0009805	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0011947	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0030148	ORPHA:308552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0000365	ORPHA:308552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:308552	Glycogen storage disease due to acid maltase deficiency, infantile onset		HP:0001249	ORPHA:308552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0002090	ORPHA:397596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0200117	ORPHA:397596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0000403	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0001744	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0002110	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0002240	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0002716	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0002960	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0003496	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0004313	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0010976	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0011109	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0011956	ORPHA:397596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0000252	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0000365	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0001369	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0001508	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0002242	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0002665	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0011110	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0012758	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0031692	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0031693	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397596	Activated PI3K-delta syndrome		HP:0032170	ORPHA:397596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313906	Congenital pancreatic cyst		HP:0000952	ORPHA:313906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313906	Congenital pancreatic cyst		HP:0001733	ORPHA:313906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313906	Congenital pancreatic cyst		HP:0002013	ORPHA:313906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313906	Congenital pancreatic cyst		HP:0002027	ORPHA:313906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313906	Congenital pancreatic cyst		HP:0002039	ORPHA:313906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313906	Congenital pancreatic cyst		HP:0003270	ORPHA:313906	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000325	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000347	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001511	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001518	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0004209	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0004482	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0008872	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0008897	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0011220	ORPHA:397590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000045	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000047	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000175	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000369	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000750	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001159	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001270	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001562	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001626	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0009237	ORPHA:397590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000023	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000028	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000048	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000821	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0000957	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001263	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001804	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0001943	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0002007	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0002099	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0006266	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0007018	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0010442	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0030260	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0100257	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0100555	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397590	Silver-Russell syndrome due to a point mutation		HP:0100607	ORPHA:397590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0000268	ORPHA:1399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0000365	ORPHA:1399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0000639	ORPHA:1399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0000815	ORPHA:1399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0001251	ORPHA:1399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0001268	ORPHA:1399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0001276	ORPHA:1399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0001288	ORPHA:1399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0001347	ORPHA:1399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0001387	ORPHA:1399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0002919	ORPHA:1399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0003693	ORPHA:1399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1399	Richards-Rundle syndrome		HP:0004349	ORPHA:1399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0000762	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0001761	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0001288	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0002378	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0002936	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0003438	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0003482	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0007141	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0007340	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0008944	ORPHA:352675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0002166	ORPHA:352675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0003236	ORPHA:352675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0003376	ORPHA:352675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0003393	ORPHA:352675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0000407	ORPHA:352675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352675	X-linked Charcot-Marie-Tooth disease type 6		HP:0001270	ORPHA:352675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0000252	ORPHA:1398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0000256	ORPHA:1398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0000496	ORPHA:1398	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0000708	ORPHA:1398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0001250	ORPHA:1398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0001251	ORPHA:1398	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0001252	ORPHA:1398	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0001276	ORPHA:1398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0002167	ORPHA:1398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1398	Isolated cerebellar agenesis		HP:0100022	ORPHA:1398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1397	Hydrocephaly-cerebellar agenesis syndrome		HP:0000518	ORPHA:1397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1397	Hydrocephaly-cerebellar agenesis syndrome		HP:0001249	ORPHA:1397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1397	Hydrocephaly-cerebellar agenesis syndrome		HP:0001251	ORPHA:1397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1397	Hydrocephaly-cerebellar agenesis syndrome		HP:0001252	ORPHA:1397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1397	Hydrocephaly-cerebellar agenesis syndrome		HP:0012642	ORPHA:1397	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000252	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000256	ORPHA:276413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000286	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000308	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000316	ORPHA:276413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000369	ORPHA:276413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000463	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000494	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000582	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000601	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0000717	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001166	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001249	ORPHA:276413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001250	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001263	ORPHA:276413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001321	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001508	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001643	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001704	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001883	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0002007	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0002308	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0002463	ORPHA:276413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0005280	ORPHA:276413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0001382	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0006695	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0007018	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0100444	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0100783	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276413	10q22.3q23.3 microdeletion syndrome		HP:0200008	ORPHA:276413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000154	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000175	ORPHA:1394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000204	ORPHA:1394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000248	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000256	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000286	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000289	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000316	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000358	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000445	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000470	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000486	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000494	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000574	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000664	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000774	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000892	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000902	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0000912	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0001249	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0001320	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0001561	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0002079	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0002119	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0002120	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0002162	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0002208	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0002650	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0002937	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0003196	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0003422	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0004322	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0010720	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0011800	ORPHA:1394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1394	Cerebrofaciothoracic dysplasia		HP:0100790	ORPHA:1394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0001386	ORPHA:98878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0002829	ORPHA:98878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0003125	ORPHA:98878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0005261	ORPHA:98878	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0011889	ORPHA:98878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0001907	ORPHA:98878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0007420	ORPHA:98878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0030140	ORPHA:98878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0002239	ORPHA:98878	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0009811	ORPHA:98878	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0012233	ORPHA:98878	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0030746	ORPHA:98878	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0002170	ORPHA:98878	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98878	Hemophilia A		HP:0012223	ORPHA:98878	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0000790	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0001058	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0002170	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0003010	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0003645	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0004406	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0004846	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0005261	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0006298	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0011858	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0012233	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0012541	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0040232	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98879	Hemophilia B		HP:0400008	ORPHA:98879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000278	ORPHA:480898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000490	ORPHA:480898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000750	ORPHA:480898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0001263	ORPHA:480898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0001999	ORPHA:480898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0007371	ORPHA:480898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0100275	ORPHA:480898	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000212	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000253	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000322	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000649	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0001212	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0001265	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0002059	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0002187	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0002509	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0002650	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0031954	ORPHA:480898	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000294	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000347	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000377	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000483	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000486	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000545	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000565	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0000648	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0001045	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0002023	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0002353	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0008755	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480898	Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome		HP:0100704	ORPHA:480898	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0001903	ORPHA:98870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0004447	ORPHA:98870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0011273	ORPHA:98870	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0001877	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0002904	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0003452	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0005518	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0012130	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0012378	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0025035	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0025196	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0025354	ORPHA:98870	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0000225	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0000980	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0002249	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0002315	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0002910	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0011891	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0030140	ORPHA:98870	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98870	Congenital dyserythropoietic anemia type III		HP:0004322	ORPHA:98870	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0000028	ORPHA:1381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0000047	ORPHA:1381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0000174	ORPHA:1381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0000486	ORPHA:1381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0000518	ORPHA:1381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0000639	ORPHA:1381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0001249	ORPHA:1381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0001636	ORPHA:1381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0002023	ORPHA:1381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0002857	ORPHA:1381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0008063	ORPHA:1381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1381	Cataract-intellectual disability-anal atresia-urinary defects syndrome		HP:0008736	ORPHA:1381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000712	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000716	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000737	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0001257	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0001260	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0001300	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0001347	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002063	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002451	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002493	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0004373	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0008760	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0100710	ORPHA:216873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000722	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0001288	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0001337	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002015	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002072	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002167	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0007256	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0012048	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0030216	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0100543	ORPHA:216873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000488	ORPHA:216873	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000618	ORPHA:216873	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000648	ORPHA:216873	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0000709	ORPHA:216873	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002312	ORPHA:216873	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0002359	ORPHA:216873	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216873	Atypical pantothenate kinase-associated neurodegeneration		HP:0012473	ORPHA:216873	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1380	Cataract-nephropathy-encephalopathy syndrome		HP:0000124	ORPHA:1380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1380	Cataract-nephropathy-encephalopathy syndrome		HP:0000518	ORPHA:1380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1380	Cataract-nephropathy-encephalopathy syndrome		HP:0000639	ORPHA:1380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1380	Cataract-nephropathy-encephalopathy syndrome		HP:0001249	ORPHA:1380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1380	Cataract-nephropathy-encephalopathy syndrome		HP:0001250	ORPHA:1380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1380	Cataract-nephropathy-encephalopathy syndrome		HP:0004322	ORPHA:1380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0003458	ORPHA:171445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0008180	ORPHA:171445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0008994	ORPHA:171445	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0001288	ORPHA:171445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0002093	ORPHA:171445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0003418	ORPHA:171445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0003551	ORPHA:171445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0003555	ORPHA:171445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0001638	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0001712	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0003691	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0009830	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0011712	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0012548	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0025168	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0030177	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0030319	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0034392	ORPHA:171445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0003326	ORPHA:171445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0003722	ORPHA:171445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0030235	ORPHA:171445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171445	Muscle filaminopathy		HP:0410011	ORPHA:171445	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0012490	ORPHA:86884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0030350	ORPHA:86884	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0001433	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0001824	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0001945	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0003256	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0012156	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0012378	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0025143	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0025474	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86884	Subcutaneous panniculitis-like T-cell lymphoma		HP:0200042	ORPHA:86884	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003198	ORPHA:171442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003458	ORPHA:171442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003798	ORPHA:171442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0002067	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003326	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003484	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003557	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003722	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003803	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0009058	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0031047	ORPHA:171442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0000218	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0000275	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0000276	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0000347	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0001265	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0001371	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0001644	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0002068	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0001288	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0002483	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0002747	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0002792	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0003552	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0007340	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0010546	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0011968	ORPHA:171442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy		HP:0008180	ORPHA:171442	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171442	Adult-onset nemaline myopathy	NOT	HP:0007010	ORPHA:171442	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0002460	ORPHA:329478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0000726	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0001437	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0002344	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0001288	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0002359	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0002380	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0003326	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0003394	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0003458	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0003691	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0003805	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0008180	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0008954	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0008978	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0009005	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0009027	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0012548	ORPHA:329478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0000020	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0000716	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0000739	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0000762	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0001300	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0001337	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0001349	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0002607	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0003418	ORPHA:329478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation		HP:0002792	ORPHA:329478	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation	NOT	HP:0001638	ORPHA:329478	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:329478	Adult-onset distal myopathy due to VCP mutation	NOT	HP:0003701	ORPHA:329478	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0000174	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0000308	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0000343	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0000649	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0001162	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0001249	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0001276	ORPHA:1389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0001347	ORPHA:1389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0002205	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0003196	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0004322	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0004326	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0011220	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1389	Cortical blindness-intellectual disability-polydactyly syndrome		HP:0100704	ORPHA:1389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000162	ORPHA:1388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000175	ORPHA:1388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000272	ORPHA:1388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000347	ORPHA:1388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0001508	ORPHA:1388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0004209	ORPHA:1388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0005930	ORPHA:1388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000293	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000358	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000389	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0001387	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0001629	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0002553	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0002650	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0004322	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0030680	ORPHA:1388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000316	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0000767	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0001631	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0002119	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0001382	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0009467	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0010285	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0010508	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1388	Catel-Manzke syndrome		HP:0100490	ORPHA:1388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0000975	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0000989	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0001744	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0001824	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0001945	ORPHA:86893	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0002039	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0002240	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0002665	ORPHA:86893	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0002716	ORPHA:86893	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0002721	ORPHA:86893	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0003002	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0005561	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0012191	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86893	Nodular lymphocyte predominant Hodgkin lymphoma		HP:0012378	ORPHA:86893	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002960	ORPHA:37042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0000818	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0000964	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0000964	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001531	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001891	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002242	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0003111	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0003212	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0005208	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0007473	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0011123	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0012393	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0025379	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0031401	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0100646	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0100651	ORPHA:37042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0000821	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001025	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001581	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001875	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001890	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001904	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001970	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001973	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002013	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002024	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002098	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002205	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002719	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002901	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002910	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002917	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0003073	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0003765	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0004326	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0006515	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0008066	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0008404	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0012115	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0012578	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0030909	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0031085	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0031104	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0031123	ORPHA:37042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0000100	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0000836	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001287	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001596	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0001744	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002090	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002583	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002595	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002716	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0002754	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0005263	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0025156	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0040288	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0100614	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:37042	Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		HP:0100806	ORPHA:37042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000028	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000044	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000218	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000221	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000232	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000248	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000252	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000272	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000322	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000347	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000358	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000518	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000601	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0000692	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0001155	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0001249	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0002120	ORPHA:1387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0002162	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0002650	ORPHA:1387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0003307	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0004322	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0005280	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0007477	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0007495	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0008388	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0008872	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0009465	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0009738	ORPHA:1387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0009832	ORPHA:1387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome		HP:0011800	ORPHA:1387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001987	ORPHA:927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002013	ORPHA:927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002018	ORPHA:927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0008947	ORPHA:927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0000712	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0000713	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0000739	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001250	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001254	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001259	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001263	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001289	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001508	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002315	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002329	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002465	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0003217	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0003348	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0004396	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0007185	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0008281	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0011968	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0012378	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0100543	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0100785	ORPHA:927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0000252	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0000708	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0000725	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0000733	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001251	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001271	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001297	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0001298	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002014	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002098	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002240	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002637	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0002863	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0006582	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0010529	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0010550	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:927	Hyperammonemia due to N-acetylglutamate synthase deficiency		HP:0031258	ORPHA:927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0001258	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0001288	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0002064	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0002395	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0003155	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0003324	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0003445	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0003487	ORPHA:329475	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0002653	ORPHA:329475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0002757	ORPHA:329475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0002829	ORPHA:329475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0004563	ORPHA:329475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0011842	ORPHA:329475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0001308	ORPHA:329475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329475	Spastic paraplegia-Paget disease of bone syndrome		HP:0007289	ORPHA:329475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001284	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001290	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001349	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001371	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001533	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001623	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001638	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001761	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001989	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002483	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002515	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002650	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002747	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002792	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003691	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0008180	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0011968	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0030192	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000508	ORPHA:171439	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001561	ORPHA:171439	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002804	ORPHA:171439	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy	NOT	HP:0007010	ORPHA:171439	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003198	ORPHA:171439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003458	ORPHA:171439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003798	ORPHA:171439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001265	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001270	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002067	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002068	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0002312	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0001288	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003306	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003546	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003552	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003557	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003690	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0003803	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0009055	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0009058	ORPHA:171439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000218	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000275	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000276	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000316	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000347	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000467	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171439	Childhood-onset nemaline myopathy		HP:0000774	ORPHA:171439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0012517	ORPHA:926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0000155	ORPHA:926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0000166	ORPHA:926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0000225	ORPHA:926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0000230	ORPHA:926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0001935	ORPHA:926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0005978	ORPHA:926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0040113	ORPHA:926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0100758	ORPHA:926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0001045	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0001300	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0002634	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0006357	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0012531	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0100605	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0100651	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:926	Acatalasemia		HP:0100753	ORPHA:926	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0000252	ORPHA:929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0000286	ORPHA:929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0000303	ORPHA:929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0000347	ORPHA:929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0000400	ORPHA:929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0000448	ORPHA:929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0001249	ORPHA:929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0001510	ORPHA:929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0002571	ORPHA:929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:929	Achalasia-microcephaly syndrome		HP:0007477	ORPHA:929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1383	Cataract-deafness-hypogonadism syndrome		HP:0000135	ORPHA:1383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1383	Cataract-deafness-hypogonadism syndrome		HP:0000407	ORPHA:1383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1383	Cataract-deafness-hypogonadism syndrome		HP:0000519	ORPHA:1383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1383	Cataract-deafness-hypogonadism syndrome		HP:0001256	ORPHA:1383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1383	Cataract-deafness-hypogonadism syndrome		HP:0004322	ORPHA:1383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1383	Cataract-deafness-hypogonadism syndrome		HP:0004554	ORPHA:1383	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000490	ORPHA:276422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000047	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000062	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000164	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000252	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000288	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000293	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000308	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000337	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000486	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000582	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000601	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0001249	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0001263	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0002381	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0030680	ORPHA:276422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000369	ORPHA:276422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000389	ORPHA:276422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000772	ORPHA:276422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0000889	ORPHA:276422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276422	10q22.3q23.3 microduplication syndrome		HP:0001636	ORPHA:276422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0002317	ORPHA:482601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003236	ORPHA:482601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003458	ORPHA:482601	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0001315	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0002091	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003551	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003700	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003731	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003805	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0007210	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0008944	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0008959	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0008994	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0009027	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0009046	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0009050	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0009053	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0009129	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0030051	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0030193	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0030319	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0031108	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0031237	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0032341	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0034391	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0034677	ORPHA:482601	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0000218	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0001639	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0002359	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0002540	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003376	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0003798	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0009072	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0012548	ORPHA:482601	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0002200	ORPHA:482601	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy		HP:0005216	ORPHA:482601	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:482601	Adenylosuccinate synthetase-like 1-related distal myopathy	NOT	HP:0003474	ORPHA:482601	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0002110	ORPHA:922	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0002257	ORPHA:922	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0002788	ORPHA:922	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0005938	ORPHA:922	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0002094	ORPHA:922	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0002098	ORPHA:922	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0011109	ORPHA:922	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:922	Familial nasal acilia		HP:0100750	ORPHA:922	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000219	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000280	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000286	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000316	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000343	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000411	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000463	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000470	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000486	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000637	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001263	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000786	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0000939	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0004209	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001182	ORPHA:96201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001249	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001250	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0002069	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001319	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001382	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001510	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001562	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001629	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001647	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001718	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001770	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0001999	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0002162	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0002616	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0009824	ORPHA:96201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0009816	ORPHA:96201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0004691	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0004349	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0010864	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0007642	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0008209	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0010945	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0011968	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0012725	ORPHA:96201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96201	X small rings syndrome		HP:0400000	ORPHA:96201	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0000767	ORPHA:98863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001315	ORPHA:98863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001387	ORPHA:98863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0002486	ORPHA:98863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003198	ORPHA:98863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003236	ORPHA:98863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0006785	ORPHA:98863	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0000470	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0000912	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001288	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001639	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0002155	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0002515	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003141	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003306	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003418	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003458	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003691	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003805	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0004631	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0008948	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0008956	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0008994	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0008997	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0011807	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0030051	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0030117	ORPHA:98863	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0000508	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001252	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001513	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001678	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001771	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0002650	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0002808	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0002987	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0003307	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0005115	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0008064	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0009125	ORPHA:98863	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001605	ORPHA:98863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0001645	ORPHA:98863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0002747	ORPHA:98863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy		HP:0005155	ORPHA:98863	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98863	X-linked Emery-Dreifuss muscular dystrophy	NOT	HP:0001249	ORPHA:98863	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001387	ORPHA:423461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0004322	ORPHA:423461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0008897	ORPHA:423461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0010471	ORPHA:423461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000212	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000280	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000286	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000293	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000403	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000405	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000470	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000943	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001072	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001371	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001653	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001659	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001288	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0002653	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0002751	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0005280	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0009023	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0012069	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0040160	ORPHA:423461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001537	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001540	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001609	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001635	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0001667	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0002505	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0002788	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0002797	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0007957	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0012185	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0100543	ORPHA:423461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000407	ORPHA:423461	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:423461	Mucolipidosis type III alpha/beta		HP:0000520	ORPHA:423461	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000028	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000047	ORPHA:921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000174	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000175	ORPHA:921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000272	ORPHA:921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000286	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000400	ORPHA:921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000405	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000407	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000482	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000567	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000589	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0000612	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0001156	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0001631	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0001770	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0001831	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0002974	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0004322	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0008743	ORPHA:921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0009465	ORPHA:921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0010751	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0012368	ORPHA:921	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:921	Abruzzo-Erickson syndrome		HP:0100542	ORPHA:921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000055	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000062	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000154	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000233	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000327	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000365	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000413	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000430	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000463	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000505	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000545	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000561	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000691	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000750	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000958	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0000963	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001000	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001126	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001263	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001510	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001537	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001539	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001582	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0001770	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0002213	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0002223	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0003187	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0005280	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0006709	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0007392	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0007957	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0008070	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0008551	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0008736	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0010669	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0010720	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0011224	ORPHA:920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0100490	ORPHA:920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:920	Ablepharon macrostomia syndrome		HP:0200020	ORPHA:920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0001288	ORPHA:216866	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0000157	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0000510	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0000543	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0000580	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0001257	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0001260	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0001347	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0002015	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0002359	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0002454	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0002533	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0002540	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0002659	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0003552	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0007018	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0007325	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0012675	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0030051	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0100543	ORPHA:216866	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0000298	ORPHA:216866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0001263	ORPHA:216866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0001824	ORPHA:216866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0002179	ORPHA:216866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0011951	ORPHA:216866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0012735	ORPHA:216866	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0000618	ORPHA:216866	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216866	Classic pantothenate kinase-associated neurodegeneration		HP:0001250	ORPHA:216866	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1377	Cataract-microcornea syndrome		HP:0000482	ORPHA:1377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1377	Cataract-microcornea syndrome		HP:0000518	ORPHA:1377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1377	Cataract-microcornea syndrome		HP:0000545	ORPHA:1377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1377	Cataract-microcornea syndrome		HP:0000612	ORPHA:1377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1377	Cataract-microcornea syndrome		HP:0000639	ORPHA:1377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1377	Cataract-microcornea syndrome		HP:0001131	ORPHA:1377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1377	Cataract-microcornea syndrome		HP:0007957	ORPHA:1377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:329466	Autosomal dominant focal dystonia, DYT25 type		HP:0004373	ORPHA:329466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:329466	Autosomal dominant focal dystonia, DYT25 type		HP:0000473	ORPHA:329466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329466	Autosomal dominant focal dystonia, DYT25 type		HP:0002451	ORPHA:329466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329466	Autosomal dominant focal dystonia, DYT25 type		HP:0002530	ORPHA:329466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329466	Autosomal dominant focal dystonia, DYT25 type		HP:0012049	ORPHA:329466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329466	Autosomal dominant focal dystonia, DYT25 type		HP:0012179	ORPHA:329466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:329466	Autosomal dominant focal dystonia, DYT25 type		HP:0031008	ORPHA:329466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0000175	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0000211	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0000377	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0000486	ORPHA:916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0001238	ORPHA:916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0001305	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0001387	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0001762	ORPHA:916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0002650	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0002664	ORPHA:916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0002828	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0003272	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0006501	ORPHA:916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:916	Aase-Smith syndrome		HP:0100490	ORPHA:916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0000174	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0000519	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0000691	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0000767	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0001249	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0002162	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0002230	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1375	Cataract-hypertrichosis-intellectual disability syndrome		HP:0005280	ORPHA:1375	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000049	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000232	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000316	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001169	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001537	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001769	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001773	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0004279	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0004322	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0100490	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0200055	ORPHA:915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000023	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000028	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000337	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000343	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000358	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000431	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000463	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000494	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000508	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000974	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0004209	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001382	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0006101	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000377	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0009890	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0100543	ORPHA:915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000164	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000175	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000202	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000204	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000286	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000311	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000327	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000470	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000485	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000486	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000684	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000708	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000767	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0000954	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001635	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001763	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0001883	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0002816	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0003319	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0005640	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0007018	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:915	Aarskog-Scott syndrome		HP:0030680	ORPHA:915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0000023	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0000191	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0000286	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0000358	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0000508	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0000518	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0001048	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0001537	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0004322	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1373	Cataract-aberrant oral frenula-growth delay syndrome		HP:0008499	ORPHA:1373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0009053	ORPHA:276435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0001265	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0001284	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0001288	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0002380	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0003236	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0003445	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0003449	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0003710	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0008985	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0008994	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0031921	ORPHA:276435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0001308	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0001337	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0002015	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0003200	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0003458	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0003805	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0006886	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0008954	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0008997	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0040132	ORPHA:276435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0002086	ORPHA:276435	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0002483	ORPHA:276435	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset		HP:0002540	ORPHA:276435	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276435	Lower motor neuron syndrome with late-adult onset	NOT	HP:0002493	ORPHA:276435	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0002435	ORPHA:268810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0045005	ORPHA:268810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0001347	ORPHA:268810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0000238	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0000805	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0001276	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0002144	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0002308	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0001288	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0002375	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0002395	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0002436	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0002607	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0003438	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0005986	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0006986	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0008467	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0010550	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0025480	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0040194	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268810	Isolated posterior meningocele		HP:0100565	ORPHA:268810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000260	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000286	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000348	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000431	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000582	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000952	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001315	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001399	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001508	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001522	ORPHA:912	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0002093	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0002240	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0002353	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0002652	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0004322	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0005280	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0006829	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0007957	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0008167	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000377	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0008872	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0010655	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0012368	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0012736	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0100543	ORPHA:912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000003	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000028	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000047	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000126	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000218	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000252	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000256	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000347	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000407	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000505	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000518	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000532	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000627	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000639	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000648	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001250	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001622	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0002021	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0002024	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0002126	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0005469	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0008665	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0009891	ORPHA:912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000157	ORPHA:912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000474	ORPHA:912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0000501	ORPHA:912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001088	ORPHA:912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001629	ORPHA:912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0001928	ORPHA:912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:912	Zellweger syndrome		HP:0008207	ORPHA:912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003306	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003418	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003458	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003691	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003805	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0004631	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0005115	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0005155	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0008948	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0008956	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0008994	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0008997	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0011807	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0030051	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0030117	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001252	ORPHA:98855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001513	ORPHA:98855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0002650	ORPHA:98855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0002808	ORPHA:98855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003307	ORPHA:98855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0008064	ORPHA:98855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0009125	ORPHA:98855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy	NOT	HP:0001249	ORPHA:98855	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0000767	ORPHA:98855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001387	ORPHA:98855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0002486	ORPHA:98855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0002600	ORPHA:98855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003198	ORPHA:98855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003236	ORPHA:98855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0006785	ORPHA:98855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0000912	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001288	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001644	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001645	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001678	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0001771	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0002155	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0002515	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0002987	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98855	Autosomal recessive Emery-Dreifuss muscular dystrophy		HP:0003141	ORPHA:98855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002718	ORPHA:911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0004429	ORPHA:911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0005390	ORPHA:911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0031381	ORPHA:911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0001508	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002028	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002090	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0004798	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0005415	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0005422	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0009098	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0200117	ORPHA:911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0000100	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0000988	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0001297	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0001433	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0001880	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002583	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002716	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002728	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002733	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002840	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0005406	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0010280	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0011274	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0100827	ORPHA:911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0001890	ORPHA:911	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0001973	ORPHA:911	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0002665	ORPHA:911	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:911	Combined immunodeficiency due to ZAP70 deficiency		HP:0005523	ORPHA:911	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0002936	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003380	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003390	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003447	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003482	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0007002	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0007078	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0009053	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0040078	ORPHA:98856	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0001284	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0001760	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0001761	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0001765	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0002460	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003376	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003387	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003693	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003701	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0007149	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0008956	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0008959	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0008994	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0009049	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0009130	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0011916	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0030237	ORPHA:98856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0002540	ORPHA:98856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003724	ORPHA:98856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0007126	ORPHA:98856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0007249	ORPHA:98856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0008988	ORPHA:98856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1		HP:0003431	ORPHA:98856	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98856	Charcot-Marie-Tooth disease type 2B1	NOT	HP:0007233	ORPHA:98856	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002044	ORPHA:913	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0100634	ORPHA:913	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002014	ORPHA:913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002018	ORPHA:913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002574	ORPHA:913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002588	ORPHA:913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0004398	ORPHA:913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0100633	ORPHA:913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0001824	ORPHA:913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0000843	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0000845	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0000854	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0000952	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0001012	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002239	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002573	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0002893	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0003072	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0003118	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0003165	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0005214	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0006767	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0008208	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0008256	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0008291	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0010783	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0011760	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0011761	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0012030	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0012032	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0012334	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0030404	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0030688	ORPHA:913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:913	Zollinger-Ellison syndrome		HP:0006744	ORPHA:913	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000270	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000473	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0001262	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0001263	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0001290	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002059	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002213	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002650	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0008897	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0010055	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0100840	ORPHA:276432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000023	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000028	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000280	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000290	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000308	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000341	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000369	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000400	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000430	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000494	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000520	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000708	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000729	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0000973	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0001254	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0001276	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0001629	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002000	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002007	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002119	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002194	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002362	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002457	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0002705	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0004415	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0009931	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0010803	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0011675	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0025104	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276432	Ogden syndrome		HP:0030149	ORPHA:276432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000028	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000135	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000164	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000252	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000365	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000407	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000486	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000491	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000498	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000518	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000524	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000613	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000621	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000648	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000656	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000958	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000962	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000963	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000992	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0000995	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001009	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001029	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001034	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001053	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001059	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001072	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001250	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001251	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001257	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001315	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001480	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001508	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001596	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001945	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002071	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002120	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002353	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002376	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002664	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002750	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002829	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0002861	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0003355	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0004322	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0004334	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0004493	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0001249	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0007759	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0008734	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0009755	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0009830	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0010649	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0010783	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0012378	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0012733	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0012740	ORPHA:910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0100012	ORPHA:910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0100543	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:910	Xeroderma pigmentosum		HP:0100585	ORPHA:910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0000767	ORPHA:98853	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001315	ORPHA:98853	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001387	ORPHA:98853	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0002486	ORPHA:98853	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003198	ORPHA:98853	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003236	ORPHA:98853	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0006785	ORPHA:98853	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0000912	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001288	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001771	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0002155	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0002515	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0002987	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003141	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003306	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003418	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003458	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003691	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003805	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0004631	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0008948	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0008956	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0008994	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0008997	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0011807	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0030051	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0030117	ORPHA:98853	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0000508	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001252	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001513	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001644	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001678	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0002650	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0002808	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0003307	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0005115	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0008064	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0009125	ORPHA:98853	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001605	ORPHA:98853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001639	ORPHA:98853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0001645	ORPHA:98853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0002747	ORPHA:98853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy		HP:0005155	ORPHA:98853	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98853	Autosomal dominant Emery-Dreifuss muscular dystrophy	NOT	HP:0001249	ORPHA:98853	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000218	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000278	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001270	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001290	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0002093	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0002515	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003323	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003391	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003551	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003700	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0009046	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0010628	ORPHA:169186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000160	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000193	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000276	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000411	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000597	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000602	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0000750	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001256	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001260	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001284	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001349	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001618	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001654	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001712	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001761	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001762	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0001999	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003273	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003307	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003403	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003687	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003691	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0003803	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169186	Autosomal recessive centronuclear myopathy		HP:0100807	ORPHA:169186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2690	Neutropenia-monocytopenia-deafness syndrome		HP:0000407	ORPHA:2690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2690	Neutropenia-monocytopenia-deafness syndrome		HP:0001874	ORPHA:2690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2690	Neutropenia-monocytopenia-deafness syndrome		HP:0004311	ORPHA:2690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2690	Neutropenia-monocytopenia-deafness syndrome		HP:0010978	ORPHA:2690	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0001518	ORPHA:90050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0001622	ORPHA:90050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0008046	ORPHA:90050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0500049	ORPHA:90050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0000486	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0000501	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0000518	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0000545	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0000618	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0000646	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0001103	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0001136	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0007663	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0007902	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90050	Retinopathy of prematurity		HP:0007917	ORPHA:90050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000256	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000407	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000480	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000494	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001249	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001263	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001328	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001520	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001629	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001634	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001999	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0004712	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0011407	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0012385	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0012471	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0030037	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0410252	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0410255	ORPHA:500095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000003	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000023	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000105	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000158	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000286	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000311	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000316	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000400	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000411	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000483	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000486	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000490	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000518	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000637	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0000750	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001172	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001176	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001707	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001762	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001833	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001840	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0001847	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0002619	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0002667	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0002982	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0003298	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0011800	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0031069	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500095	Tall stature-intellectual disability-renal anomalies syndrome		HP:0100694	ORPHA:500095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0001269	ORPHA:306741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0001332	ORPHA:306741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0002518	ORPHA:306741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0012751	ORPHA:306741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0001787	ORPHA:306741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0002451	ORPHA:306741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0100556	ORPHA:306741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0000245	ORPHA:306741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0000250	ORPHA:306741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0001250	ORPHA:306741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0003487	ORPHA:306741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0007256	ORPHA:306741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0010540	ORPHA:306741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0001270	ORPHA:306741	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:306741	Hemidystonia-hemiatrophy syndrome		HP:0012106	ORPHA:306741	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0001945	ORPHA:50839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0002716	ORPHA:50839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0030350	ORPHA:50839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0002039	ORPHA:50839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0033834	ORPHA:50839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0000541	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0001369	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0001433	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0001824	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0002027	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0002829	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0003326	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0003565	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0011227	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0012121	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0020161	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0020165	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0032118	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0100653	ORPHA:50839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0002754	ORPHA:50839	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0033430	ORPHA:50839	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50839	Cat-scratch disease		HP:0100584	ORPHA:50839	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0000407	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0000505	ORPHA:1368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0000519	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0000639	ORPHA:1368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0000762	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0001251	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0001256	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0001276	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0001284	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0001337	ORPHA:1368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0004322	ORPHA:1368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0008615	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1368	Cataract-ataxia-deafness syndrome		HP:0009830	ORPHA:1368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0010824	ORPHA:137596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0012155	ORPHA:137596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0007924	ORPHA:137596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0000483	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0000495	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0000559	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0000622	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0000632	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0000819	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0012040	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0012122	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0012804	ORPHA:137596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0012533	ORPHA:137596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0100583	ORPHA:137596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:137596	Neurotrophic keratopathy		HP:0100963	ORPHA:137596	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0000505	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0000518	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0000982	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0000987	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0001387	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0001482	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0007418	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0008065	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0008404	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1366	Autosomal recessive palmoplantar keratoderma and congenital alopecia		HP:0100679	ORPHA:1366	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0007663	ORPHA:137599	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0007765	ORPHA:137599	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0012040	ORPHA:137599	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0012108	ORPHA:137599	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0000622	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0007812	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0007906	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0009926	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0012039	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0012155	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0030953	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0031448	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0100583	ORPHA:137599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0000491	ORPHA:137599	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0000618	ORPHA:137599	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0011134	ORPHA:137599	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:137599	Herpes simplex virus stromal keratitis		HP:0033834	ORPHA:137599	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0001257	ORPHA:352641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002073	ORPHA:352641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0003487	ORPHA:352641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0000570	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0000639	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0001348	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002015	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002061	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002066	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002464	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0003477	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0007141	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0007256	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0010831	ORPHA:352641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0000020	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0000407	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0001761	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002059	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002166	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002346	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002650	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0003693	ORPHA:352641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0001256	ORPHA:352641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity		HP:0002078	ORPHA:352641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity	NOT	HP:0004905	ORPHA:352641	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:352641	Autosomal recessive cerebellar ataxia with late-onset spasticity	NOT	HP:0100513	ORPHA:352641	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:697160	Infantile epileptic spasms syndrome		HP:0001336	ORPHA:697160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:697160	Infantile epileptic spasms syndrome		HP:0002376	ORPHA:697160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:697160	Infantile epileptic spasms syndrome		HP:0002521	ORPHA:697160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:697160	Infantile epileptic spasms syndrome		HP:0012469	ORPHA:697160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:697160	Infantile epileptic spasms syndrome		HP:0000707	ORPHA:697160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:697160	Infantile epileptic spasms syndrome		HP:0011121	ORPHA:697160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1361	Carnosinase deficiency		HP:0001249	ORPHA:1361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1361	Carnosinase deficiency		HP:0002123	ORPHA:1361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1361	Carnosinase deficiency		HP:0002353	ORPHA:1361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1361	Carnosinase deficiency		HP:0002376	ORPHA:1361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1361	Carnosinase deficiency		HP:0003167	ORPHA:1361	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0000822	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001050	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001899	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0011106	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0020059	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0025548	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0025619	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0100724	ORPHA:90041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0000739	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0000848	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001513	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0002149	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0002152	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0002155	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0002315	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0002321	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0003124	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0003394	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0004950	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0005117	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0012378	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0012605	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0025502	ORPHA:90041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001082	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001297	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001658	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001677	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001681	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0002094	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0004398	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0100785	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0410019	ORPHA:90041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0000121	ORPHA:90041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0000819	ORPHA:90041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome		HP:0001997	ORPHA:90041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90041	Gaisböck syndrome	NOT	HP:0001744	ORPHA:90041	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0000421	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0000989	ORPHA:90042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0001892	ORPHA:90042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0001901	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0001907	ORPHA:90042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0002027	ORPHA:90042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0002094	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0002315	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0002321	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0002829	ORPHA:90042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0002875	ORPHA:90042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0004936	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0011902	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0012378	ORPHA:90042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90042	Primary familial polycythemia		HP:0012735	ORPHA:90042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2695	Bifid nose		HP:0000316	ORPHA:2695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2695	Bifid nose		HP:0011803	ORPHA:2695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0000338	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0000496	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0000508	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0000975	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001251	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001260	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001263	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001276	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001285	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001288	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001290	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001300	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001332	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001337	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001611	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0001760	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0002075	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0002310	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0002360	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0002362	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0002421	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0002451	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0002597	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0005484	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0008936	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0010307	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0010553	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0011443	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0012378	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0030215	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352649	Brain dopamine-serotonin vesicular transport disease		HP:0100543	ORPHA:352649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90044	Familial pseudohyperkalemia		HP:0002153	ORPHA:90044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90044	Familial pseudohyperkalemia		HP:0000822	ORPHA:90044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90044	Familial pseudohyperkalemia		HP:0004446	ORPHA:90044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90044	Familial pseudohyperkalemia		HP:0001923	ORPHA:90044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90044	Familial pseudohyperkalemia		HP:0005518	ORPHA:90044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90044	Familial pseudohyperkalemia		HP:0004802	ORPHA:90044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0000010	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0000206	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0000708	ORPHA:90045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0000980	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001250	ORPHA:90045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001263	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001347	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001508	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001873	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001876	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001880	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0001889	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002014	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002017	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002020	ORPHA:90045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002039	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002205	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002514	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002715	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0002721	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0003202	ORPHA:90045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0004313	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0009830	ORPHA:90045	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0100022	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90045	Hereditary folate malabsorption		HP:0100825	ORPHA:90045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0003687	ORPHA:169189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0000508	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0000883	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0001290	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0001436	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0001520	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0001558	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0001561	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0002194	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0001288	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0003458	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0003803	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0004488	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0005268	ORPHA:169189	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0008180	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0008994	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0008997	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0010546	ORPHA:169189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0000020	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0000028	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0000544	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0001048	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0002021	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0002522	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0002747	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0003477	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0003738	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0008981	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0012768	ORPHA:169189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169189	Autosomal dominant centronuclear myopathy		HP:0002047	ORPHA:169189	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0001531	ORPHA:2697	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0002804	ORPHA:2697	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000124	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000962	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0001249	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0001994	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0002028	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0002240	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0002719	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0002908	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0006566	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0007370	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0008064	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0008780	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0011873	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0012483	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0030402	ORPHA:2697	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000121	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000252	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000365	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000369	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000821	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000938	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0000973	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0001252	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0001558	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0001562	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0002756	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0003202	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0005248	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome		HP:0009806	ORPHA:2697	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2697	Arthrogryposis-renal dysfunction-cholestasis syndrome	NOT	HP:0030948	ORPHA:2697	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2698	Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		HP:0001820	ORPHA:2698	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2698	Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		HP:0008527	ORPHA:2698	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2698	Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		HP:0032541	ORPHA:2698	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2698	Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		HP:0000972	ORPHA:2698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2698	Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		HP:0000982	ORPHA:2698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2698	Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		HP:0000410	ORPHA:2698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2698	Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome		HP:0045059	ORPHA:2698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0000486	ORPHA:1369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0000501	ORPHA:1369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0000512	ORPHA:1369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0000518	ORPHA:1369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0000545	ORPHA:1369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0000639	ORPHA:1369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0001131	ORPHA:1369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0001639	ORPHA:1369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0003128	ORPHA:1369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1369	Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome		HP:0003198	ORPHA:1369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2680	Hypomyelination neuropathy-arthrogryposis syndrome		HP:0001252	ORPHA:2680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2680	Hypomyelination neuropathy-arthrogryposis syndrome		HP:0001315	ORPHA:2680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2680	Hypomyelination neuropathy-arthrogryposis syndrome		HP:0001376	ORPHA:2680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2680	Hypomyelination neuropathy-arthrogryposis syndrome		HP:0002098	ORPHA:2680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2680	Hypomyelination neuropathy-arthrogryposis syndrome		HP:0003457	ORPHA:2680	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0000980	ORPHA:544482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001873	ORPHA:544482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001878	ORPHA:544482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001919	ORPHA:544482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0012378	ORPHA:544482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0032169	ORPHA:544482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0000707	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001945	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001974	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002014	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002027	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0011037	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0011115	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0011116	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0011947	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0030783	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0032155	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0100282	ORPHA:544482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0000822	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0000969	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001287	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001733	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002013	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002018	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002090	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002094	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002102	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002153	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002901	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002902	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0004372	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0005208	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0012593	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0012819	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0025085	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0031691	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0031864	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0100519	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0100520	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0100735	ORPHA:544482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0000819	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001250	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001259	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0001269	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0002576	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0003095	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0005244	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0007430	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0011919	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0030049	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0031368	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:544482	Infection-related hemolytic uremic syndrome		HP:0100704	ORPHA:544482	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0000182	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0000273	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0000708	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0000712	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0000719	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0000722	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0000737	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0001260	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0001290	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0002072	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0002315	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0002317	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0100248	ORPHA:306731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0003095	ORPHA:306731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0005366	ORPHA:306731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0010783	ORPHA:306731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306731	Sydenham chorea		HP:0100584	ORPHA:306731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0000980	ORPHA:90037	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0001324	ORPHA:90037	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0001635	ORPHA:90037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0001649	ORPHA:90037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0001744	ORPHA:90037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0001890	ORPHA:90037	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0002315	ORPHA:90037	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0002875	ORPHA:90037	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0003573	ORPHA:90037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0012086	ORPHA:90037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90037	Drug-induced autoimmune hemolytic anemia		HP:0012378	ORPHA:90037	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001873	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001919	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001937	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002013	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002014	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002027	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0003259	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0005423	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0008282	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0100519	ORPHA:90038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0000707	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0000737	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0000822	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001250	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001262	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001923	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001944	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001974	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001981	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002900	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002902	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0003641	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0025085	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0025435	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0031368	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0100282	ORPHA:90038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001259	ORPHA:90038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001658	ORPHA:90038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0001733	ORPHA:90038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002035	ORPHA:90038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002576	ORPHA:90038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0002586	ORPHA:90038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90038	Shiga toxin-associated hemolytic uremic syndrome		HP:0012851	ORPHA:90038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0000160	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0000163	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0000311	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0000457	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0000463	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0003196	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0004322	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0005599	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0007440	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0007477	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0030680	ORPHA:1355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1355	Congenital heart defect-round face-developmental delay syndrome		HP:0000047	ORPHA:1355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0001332	ORPHA:306734	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0000473	ORPHA:306734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0000643	ORPHA:306734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0002268	ORPHA:306734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0004373	ORPHA:306734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0007325	ORPHA:306734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0002451	ORPHA:306734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0002530	ORPHA:306734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:306734	Primary dystonia, DYT21 type		HP:0012049	ORPHA:306734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0005560	ORPHA:90039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0011902	ORPHA:90039	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0011905	ORPHA:90039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0011906	ORPHA:90039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0011907	ORPHA:90039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0025066	ORPHA:90039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0025547	ORPHA:90039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0045048	ORPHA:90039	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0030058	ORPHA:90039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0045047	ORPHA:90039	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0000980	ORPHA:90039	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0001744	ORPHA:90039	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0001903	ORPHA:90039	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90039	Hemoglobin D disease		HP:0002027	ORPHA:90039	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0000772	ORPHA:1354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0000774	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0000944	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0001522	ORPHA:1354	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0001629	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0001631	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0001633	ORPHA:1354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0001702	ORPHA:1354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0002808	ORPHA:1354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0003312	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0003498	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0004414	ORPHA:1354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0005026	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1354	Heart defects-limb shortening syndrome		HP:0005616	ORPHA:1354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000256	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000316	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000400	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000414	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000490	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000653	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000718	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001263	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001319	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001488	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001520	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001561	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001792	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0002003	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0002223	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0007018	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0008689	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0012520	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0030890	ORPHA:544488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000023	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000278	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000337	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000384	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000407	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000494	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000561	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000581	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000708	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000902	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0000960	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001182	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001250	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001257	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001344	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001596	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0001800	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0002099	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0002209	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0002334	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0002465	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0002608	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0004209	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0006956	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0006989	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0007074	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0007082	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0007109	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0010880	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0011276	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0011309	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0012450	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0032152	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0032671	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0045075	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0100716	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:544488	Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome		HP:0410018	ORPHA:544488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000119	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000252	ORPHA:1352	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000347	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000364	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000378	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000431	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000486	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000568	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000581	ORPHA:1352	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0000582	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0001107	ORPHA:1352	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0001336	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0001511	ORPHA:1352	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0001545	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0001671	ORPHA:1352	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0002023	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0003022	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0003974	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0004209	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0008551	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0009601	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1352	Atrioventricular defect-blepharophimosis-radial and anal defect syndrome		HP:0010035	ORPHA:1352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0000407	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0000556	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0000572	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0000648	ORPHA:49827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0000819	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0000980	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001254	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001297	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001629	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001631	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001635	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001695	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001873	ORPHA:49827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0001889	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0002014	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0002039	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0002315	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0003401	ORPHA:49827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0004322	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49827	Thiamine-responsive megaloblastic anemia syndrome		HP:0006671	ORPHA:49827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0000889	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0001156	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0001387	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0002983	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0003043	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0031095	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0006501	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0009601	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0009811	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0011675	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0040071	ORPHA:1350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0001161	ORPHA:1350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0005916	ORPHA:1350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0010044	ORPHA:1350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0010047	ORPHA:1350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0000028	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0000164	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0000174	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0001249	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0001555	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0002162	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0003019	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0009908	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0030680	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1350	Heart-hand syndrome type 2		HP:0100556	ORPHA:1350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0000980	ORPHA:90033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0001890	ORPHA:90033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0002315	ORPHA:90033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0002875	ORPHA:90033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0002960	ORPHA:90033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0012378	ORPHA:90033	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0001744	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0001923	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0001962	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0002829	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0003641	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0004835	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0005523	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0008282	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0020062	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0020181	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0025435	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0032366	ORPHA:90033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0000952	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0001635	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0001649	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0001945	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0002725	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0005550	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0012086	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0030848	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90033	Autoimmune hemolytic anemia, warm type		HP:0100749	ORPHA:90033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0000246	ORPHA:2686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0002315	ORPHA:2686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0002653	ORPHA:2686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0040289	ORPHA:2686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0000155	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0000230	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0001581	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0001954	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0002716	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0011110	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0011947	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0012378	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0025289	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0025439	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0030757	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0032323	ORPHA:2686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0000388	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0000704	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0001873	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0001888	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0002027	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0006308	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0006357	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0009789	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0031690	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0031891	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0100658	ORPHA:2686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0002586	ORPHA:2686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0004387	ORPHA:2686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0031864	ORPHA:2686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0032169	ORPHA:2686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2686	Cyclic neutropenia		HP:0100806	ORPHA:2686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0001890	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0001945	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0002014	ORPHA:90035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0002017	ORPHA:90035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0002205	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0002315	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0002829	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0003418	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0003641	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0004844	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90035	Paroxysmal cold hemoglobinuria		HP:0012086	ORPHA:90035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0000158	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0000239	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0000271	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0000280	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0000821	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0000952	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0001252	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0001263	ORPHA:95720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0001510	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0002019	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0003270	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0004322	ORPHA:95720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0005990	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0010864	ORPHA:95720	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95720	Thyroid hypoplasia		HP:0012378	ORPHA:95720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001580	ORPHA:1359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000138	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000845	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000866	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000870	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001003	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001074	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0003118	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0005585	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0007565	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0010785	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0010788	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0011672	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0011760	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0030269	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0030428	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100619	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100814	ORPHA:1359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000008	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000053	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000199	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000708	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000771	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000798	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000822	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000978	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001007	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001065	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001297	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001324	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001507	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001635	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001907	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0004324	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0006753	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0010619	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0010732	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0012041	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0012206	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0012743	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0012887	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0025274	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0025318	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0025383	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0025451	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0030038	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0030072	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0030075	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100008	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100013	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100618	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100638	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100737	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100751	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0500011	ORPHA:1359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000098	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0000826	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0001402	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0002890	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0002894	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0002895	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0004944	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0006731	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1359	Carney complex		HP:0100743	ORPHA:1359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000126	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000162	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000175	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000201	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000218	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000233	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000252	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000286	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000343	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000347	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000463	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000494	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000508	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000634	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0000807	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0001156	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0001249	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0001252	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0001510	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0001600	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0001602	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0001762	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0002119	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0002514	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0002650	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0003196	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0003198	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0003202	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0004322	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0006824	ORPHA:1358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0007360	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0009465	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0009751	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0010295	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0010628	ORPHA:1358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1358	Carey-Fineman-Ziter syndrome		HP:0100735	ORPHA:1358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0000980	ORPHA:90036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0000988	ORPHA:90036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0001324	ORPHA:90036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0001649	ORPHA:90036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0001890	ORPHA:90036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0001945	ORPHA:90036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0002665	ORPHA:90036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0002725	ORPHA:90036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0002829	ORPHA:90036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0002875	ORPHA:90036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0002960	ORPHA:90036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0003573	ORPHA:90036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0012086	ORPHA:90036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90036	Mixed-type autoimmune hemolytic anemia		HP:0012378	ORPHA:90036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0001875	ORPHA:2688	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0005202	ORPHA:2688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0001888	ORPHA:2688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0002718	ORPHA:2688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0002719	ORPHA:2688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0005561	ORPHA:2688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0001945	ORPHA:2688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0003496	ORPHA:2688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0011107	ORPHA:2688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0012139	ORPHA:2688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0012312	ORPHA:2688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0031020	ORPHA:2688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0002841	ORPHA:2688	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia		HP:0012311	ORPHA:2688	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2688	Adult idiopathic neutropenia	NOT	HP:0003453	ORPHA:2688	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0002719	ORPHA:169160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0001888	ORPHA:169160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0001945	ORPHA:169160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0003460	ORPHA:169160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0004315	ORPHA:169160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0008866	ORPHA:169160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0031381	ORPHA:169160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0045080	ORPHA:169160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0000388	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0001019	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0001433	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0001880	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0002014	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0002039	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0002090	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0002722	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0004385	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0005353	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0005401	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0006532	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0009098	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0010702	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169160	T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta		HP:0012115	ORPHA:169160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0000343	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0000470	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0000829	ORPHA:50810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0000878	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001181	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001250	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001252	ORPHA:50810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001263	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001276	ORPHA:50810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001284	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001321	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001339	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001508	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0001561	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0002098	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0002353	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0002983	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0003196	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0004554	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0005484	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0007598	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0010945	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0100530	ORPHA:50810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0100540	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50810	Microlissencephaly-micromelia syndrome		HP:0000280	ORPHA:50810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0000407	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0000938	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0001249	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0001263	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0001508	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0001511	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0001518	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0001533	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0004322	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0004993	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0005328	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0009064	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50811	Lipodystrophy-intellectual disability-deafness syndrome		HP:0100959	ORPHA:50811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000218	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000252	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000286	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000298	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000307	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000348	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000431	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000463	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000582	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0000953	ORPHA:50812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0001252	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0001263	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0001265	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0001508	ORPHA:50812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0001511	ORPHA:50812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0001596	ORPHA:50812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0002007	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0002240	ORPHA:50812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0002299	ORPHA:50812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0004322	ORPHA:50812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0007598	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50812	Zellweger-like syndrome without peroxisomal anomalies		HP:0010864	ORPHA:50812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000154	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000218	ORPHA:50814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000233	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000239	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000316	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000319	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000327	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000336	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000343	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000426	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000445	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000670	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000684	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000685	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000691	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000750	ORPHA:50814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000774	ORPHA:50814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0000953	ORPHA:50814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0001000	ORPHA:50814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0001763	ORPHA:50814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0002007	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0002208	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0002299	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0002650	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0002652	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0004322	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0004331	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0005306	ORPHA:50814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0001382	ORPHA:50814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0006480	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0008031	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0008070	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0008444	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50814	Craniolenticulosutural dysplasia		HP:0008808	ORPHA:50814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000175	ORPHA:50815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000377	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000384	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000396	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000405	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000407	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000410	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000413	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000483	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0000486	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0001328	ORPHA:50815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0004322	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0004452	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0004467	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0007427	ORPHA:50815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0008774	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0009795	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0009796	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0009839	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0009882	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50815	Branchiogenic deafness syndrome		HP:0011272	ORPHA:50815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2678	Familial isolated café-au-lait macules		HP:0001480	ORPHA:2678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2678	Familial isolated café-au-lait macules		HP:0007565	ORPHA:2678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0009830	ORPHA:90026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0010783	ORPHA:90026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0032147	ORPHA:90026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0000989	ORPHA:90026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0001872	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0001909	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0002045	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0002205	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0002633	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0002936	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0010741	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0012533	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0012534	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90026	Primary erythromelalgia		HP:0200101	ORPHA:90026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0011437	ORPHA:95715	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0030057	ORPHA:95715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0000260	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0000958	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0001265	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0001537	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0002019	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0002926	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0011968	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0031098	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0031219	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0031507	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0100786	ORPHA:95715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0000280	ORPHA:95715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0001319	ORPHA:95715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0002908	ORPHA:95715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0006579	ORPHA:95715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0025379	ORPHA:95715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0025483	ORPHA:95715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies		HP:0500011	ORPHA:95715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95715	Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies	NOT	HP:0000853	ORPHA:95715	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0000518	ORPHA:1345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0000822	ORPHA:1345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0000926	ORPHA:1345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0001387	ORPHA:1345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0001635	ORPHA:1345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0001639	ORPHA:1345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0001654	ORPHA:1345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0002204	ORPHA:1345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0002652	ORPHA:1345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0002758	ORPHA:1345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0004420	ORPHA:1345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0005108	ORPHA:1345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0010885	ORPHA:1345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1345	Cardiomyopathy-cataract-hip spine disease syndrome		HP:0011675	ORPHA:1345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0012758	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0000158	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0000282	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0001249	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0001252	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0001254	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0001265	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0001662	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0002045	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0003265	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0005280	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0025482	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0025483	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0031219	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0031220	ORPHA:95716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0000407	ORPHA:95716	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis	NOT	HP:0011437	ORPHA:95716	TAS					H	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0002925	ORPHA:95716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0031507	ORPHA:95716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0000270	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0000851	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0000853	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0001537	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0002019	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0004491	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0005930	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0006579	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0008263	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0008828	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95716	Familial thyroid dyshormonogenesis		HP:0008872	ORPHA:95716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0000158	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0000239	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0000271	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0000280	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0000821	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0001252	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0001324	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0002019	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0003270	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0008191	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0011968	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0012378	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0025483	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0100786	ORPHA:95713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0000282	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0001254	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0001263	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0001510	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0001537	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0001615	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0004322	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0006579	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0008282	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0010864	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95713	Athyreosis		HP:0033850	ORPHA:95713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001962	ORPHA:1344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0005155	ORPHA:1344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0025478	ORPHA:1344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0031546	ORPHA:1344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0031595	ORPHA:1344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001627	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0002094	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0003560	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0011675	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0011704	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0011712	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0012378	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0012664	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0030682	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0030973	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0410174	ORPHA:1344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001260	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001279	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001371	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001635	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001638	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001662	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0001907	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0002018	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0002140	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0002301	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0002315	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0002321	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0002381	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0003202	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0004756	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1344	Isolated atrial standstill		HP:0011707	ORPHA:1344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0001508	ORPHA:91359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0002207	ORPHA:91359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0002883	ORPHA:91359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0012418	ORPHA:91359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0012735	ORPHA:91359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0025179	ORPHA:91359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0032341	ORPHA:91359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0000961	ORPHA:91359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0001945	ORPHA:91359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0002098	ORPHA:91359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0002789	ORPHA:91359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0030864	ORPHA:91359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91359	Chronic pneumonitis of infancy		HP:0100721	ORPHA:91359	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0001510	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0001537	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0002019	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0003270	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0008191	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0012378	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0100786	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000854	ORPHA:95719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000872	ORPHA:95719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0002925	ORPHA:95719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0011788	ORPHA:95719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0025379	ORPHA:95719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0025388	ORPHA:95719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0032069	ORPHA:95719	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000843	ORPHA:95719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0002895	ORPHA:95719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0100647	ORPHA:95719	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0002865	ORPHA:95719	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0006731	ORPHA:95719	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0011780	ORPHA:95719	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000158	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000239	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000271	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000280	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0000952	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0001252	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95719	Thyroid hemiagenesis		HP:0001263	ORPHA:95719	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000276	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000280	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000293	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000391	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000463	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000478	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000499	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000504	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000637	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000958	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000982	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001249	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001252	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001263	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001531	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001631	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001642	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001654	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002167	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002213	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002299	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0004322	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0007392	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0008872	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0009891	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0030680	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0100840	ORPHA:1340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000028	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000218	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000256	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000286	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000316	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000343	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000348	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000358	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000400	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000465	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000470	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000486	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000494	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000508	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000545	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000639	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000767	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000962	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000974	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001003	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001048	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001622	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002007	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002162	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002217	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002353	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002650	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0003196	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0004422	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0005280	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0006191	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0007440	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0007565	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0008064	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0008070	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0008391	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0010669	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0040071	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0200102	ORPHA:1340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000126	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000176	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000238	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0000648	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001004	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001260	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001582	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0001639	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002120	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002857	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0002967	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0011024	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1340	Cardiofaciocutaneous syndrome		HP:0012719	ORPHA:1340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0002925	ORPHA:95717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0031507	ORPHA:95717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0000270	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0001537	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0002019	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0004491	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0005930	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0006579	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0008828	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0008872	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0012758	ORPHA:95717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0000158	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0000282	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0001252	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0001254	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0001265	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0001662	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0002045	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0003265	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism		HP:0005280	ORPHA:95717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism	NOT	HP:0011437	ORPHA:95717	TAS					H	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism	NOT	HP:0030057	ORPHA:95717	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism	NOT	HP:0031219	ORPHA:95717	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:95717	Idiopathic congenital hypothyroidism	NOT	HP:0031220	ORPHA:95717	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0040075	ORPHA:91350	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000505	ORPHA:91350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000870	ORPHA:91350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0007924	ORPHA:91350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0012505	ORPHA:91350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0030521	ORPHA:91350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0030591	ORPHA:91350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000044	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000238	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000830	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000871	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0002315	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0002516	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0007807	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0008240	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0011735	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0012246	ORPHA:91350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000651	ORPHA:91350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0000873	ORPHA:91350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0002170	ORPHA:91350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0004372	ORPHA:91350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0008245	ORPHA:91350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0030907	ORPHA:91350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91350	Pituitary deficiency due to Rathke cleft cysts		HP:0430022	ORPHA:91350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0001967	ORPHA:2670	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0008677	ORPHA:2670	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0000083	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0000518	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0000639	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0001104	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0001252	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0001263	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0001270	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0001562	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0008872	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0025492	ORPHA:2670	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0000505	ORPHA:2670	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0001265	ORPHA:2670	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0007676	ORPHA:2670	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0007968	ORPHA:2670	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2670	Pierson syndrome		HP:0034375	ORPHA:2670	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000252	ORPHA:2671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000340	ORPHA:2671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001511	ORPHA:2671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0008064	ORPHA:2671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0012471	ORPHA:2671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0012639	ORPHA:2671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0100679	ORPHA:2671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000062	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000135	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000153	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000211	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000232	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000288	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000316	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000400	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000457	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000520	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000951	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001176	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001302	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001305	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001321	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001331	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001339	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001371	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001460	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001558	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001561	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001769	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002126	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002179	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002269	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002334	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002536	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0003202	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0003241	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0003394	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0003560	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001302	ORPHA:2671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000175	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000176	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000193	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000269	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000278	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000347	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000492	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000499	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000518	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000614	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000938	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0000939	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001059	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0001595	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002089	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002119	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002414	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002514	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002650	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002748	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002749	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002804	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0002983	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2671	Neu-Laxova syndrome		HP:0030680	ORPHA:2671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0001251	ORPHA:2672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0001257	ORPHA:2672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0001276	ORPHA:2672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0002063	ORPHA:2672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0003552	ORPHA:2672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0001265	ORPHA:2672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0001284	ORPHA:2672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0001382	ORPHA:2672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0100022	ORPHA:2672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0000708	ORPHA:2672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0001252	ORPHA:2672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0002300	ORPHA:2672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0002381	ORPHA:2672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2672	Neuhauser-Eichner-Opitz syndrome		HP:0010529	ORPHA:2672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000248	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000369	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000413	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000426	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0001199	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0001249	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0001252	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0001511	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0004322	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0005916	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000377	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0009896	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0009912	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0010650	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0011220	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0011830	ORPHA:2673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000028	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000122	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000286	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000288	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000303	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000316	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000494	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000508	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0000767	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0001131	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0001357	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0009811	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0009832	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2673	Neurofaciodigitorenal syndrome		HP:0030680	ORPHA:2673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000830	ORPHA:91351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0002017	ORPHA:91351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0010885	ORPHA:91351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0011750	ORPHA:91351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000135	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000141	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000651	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000870	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000871	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000876	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0002331	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0003324	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0007663	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0010514	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0012505	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0030907	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0100829	ORPHA:91351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0000798	ORPHA:91351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0001250	ORPHA:91351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0001287	ORPHA:91351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0011442	ORPHA:91351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0011730	ORPHA:91351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0001117	ORPHA:91351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91351	Pituitary dermoid and epidermoid cysts		HP:0001959	ORPHA:91351	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0000802	ORPHA:91354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0000876	ORPHA:91354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0002315	ORPHA:91354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0000824	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0000826	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0000870	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0001250	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0002921	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0002960	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0007663	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0008245	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0011446	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0011748	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0030532	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0040075	ORPHA:91354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0000651	ORPHA:91354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0000863	ORPHA:91354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0002615	ORPHA:91354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0002902	ORPHA:91354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome		HP:0100661	ORPHA:91354	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91354	Pituitary deficiency due to empty sella turcica syndrome	NOT	HP:0002893	ORPHA:91354	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90023	Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency		HP:0000280	ORPHA:90023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90023	Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency		HP:0001875	ORPHA:90023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90023	Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency		HP:0002721	ORPHA:90023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90023	Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency		HP:0004322	ORPHA:90023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90023	Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency		HP:0005599	ORPHA:90023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90023	Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency		HP:0006538	ORPHA:90023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90023	Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency		HP:0007443	ORPHA:90023	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0010864	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0012378	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:6000855	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0001618	ORPHA:95712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0002015	ORPHA:95712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0100028	ORPHA:95712	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000158	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000239	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000271	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000280	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000820	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000821	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000952	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0001252	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0001324	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0001537	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0002019	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0002925	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0003270	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0100029	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0100786	ORPHA:95712	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0000958	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0001263	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0001510	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0001609	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95712	Thyroid ectopia		HP:0004322	ORPHA:95712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0000407	ORPHA:1349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001251	ORPHA:1349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001288	ORPHA:1349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001324	ORPHA:1349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001350	ORPHA:1349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001639	ORPHA:1349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0011342	ORPHA:1349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0000590	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0000597	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001268	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001298	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001635	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001644	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0002094	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0002151	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0003200	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0003457	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0003542	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0003546	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0012514	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0030680	ORPHA:1349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0000822	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001012	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0001347	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0002373	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0003326	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0009126	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0009830	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0012378	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1349	Mitochondrial DNA-related cardiomyopathy and hearing loss		HP:0100749	ORPHA:1349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000455	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000689	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001363	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001385	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001510	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001627	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001629	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002282	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002342	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002465	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002540	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002650	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002711	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002714	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0003763	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0010864	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0010880	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0031936	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000175	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000193	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000280	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000405	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000407	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000411	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000430	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000476	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000508	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000540	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000637	ORPHA:352665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001252	ORPHA:352665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000028	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000076	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000126	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000158	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000194	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000252	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000276	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000431	ORPHA:352665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000545	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000586	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000587	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000589	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000609	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000821	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000938	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0000975	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001250	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001274	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001284	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001315	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001324	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001382	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001548	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001631	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001647	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001762	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001763	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0001954	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002019	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002046	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002079	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002263	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002558	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002572	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002578	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002579	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002705	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0002877	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0003186	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0003388	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0003422	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0004389	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0004442	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0004443	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0004467	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0004942	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0005487	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0006481	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0007328	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0007655	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0008872	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0009794	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0009804	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0010297	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0010807	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0011147	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0011330	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0011470	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0011807	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352665	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion		HP:0100259	ORPHA:352665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000098	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000276	ORPHA:90024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000307	ORPHA:90024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000316	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000347	ORPHA:90024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000365	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000407	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000430	ORPHA:90024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000431	ORPHA:90024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000448	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000486	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000494	ORPHA:90024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000664	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000668	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000687	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000691	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0000698	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0001291	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0008499	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0008551	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0010609	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0011069	ORPHA:90024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90024	Deafness with labyrinthine aplasia, microtia, and microdontia		HP:0011372	ORPHA:90024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001249	ORPHA:480864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001263	ORPHA:480864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002151	ORPHA:480864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002919	ORPHA:480864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0003115	ORPHA:480864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0003236	ORPHA:480864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0003458	ORPHA:480864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0000750	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001250	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001251	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001657	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001943	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001987	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002071	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002283	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002311	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002376	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002579	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002910	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0003128	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0004305	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0008223	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0008872	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0008942	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0011343	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0011675	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0031936	ORPHA:480864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0000605	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0000639	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0000646	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0000648	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001276	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001297	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001332	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0001347	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002015	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002069	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002123	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002169	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002173	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0002384	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0003487	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0010818	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0011342	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0011344	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0012469	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0031165	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0045045	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0100704	ORPHA:480864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0000252	ORPHA:480864	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:480864	Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome		HP:0000407	ORPHA:480864	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0030016	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0030018	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000407	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000651	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000872	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001324	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001513	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001662	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001962	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002019	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002321	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002829	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002902	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0003493	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0004396	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0007041	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0025143	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0030907	ORPHA:91355	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000709	ORPHA:91355	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000863	ORPHA:91355	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001259	ORPHA:91355	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000871	ORPHA:91355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000876	ORPHA:91355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0008163	ORPHA:91355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0008240	ORPHA:91355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0011735	ORPHA:91355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0011748	ORPHA:91355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0012432	ORPHA:91355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000141	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000622	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000802	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000958	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0000980	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001278	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001895	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0001943	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002018	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002215	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002225	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0002315	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0003158	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0003187	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0007987	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0008202	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0008213	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0008214	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0008245	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0011734	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91355	Sheehan syndrome		HP:0012504	ORPHA:91355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000766	ORPHA:1335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000776	ORPHA:1335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001539	ORPHA:1335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001629	ORPHA:1335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001697	ORPHA:1335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0030680	ORPHA:1335	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001631	ORPHA:1335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0002089	ORPHA:1335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000047	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000104	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000110	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000175	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000202	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0000238	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001171	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001636	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001748	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0001883	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0002084	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0002323	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0002650	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0002992	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0006501	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0011467	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1335	Pentalogy of Cantrell		HP:0100335	ORPHA:1335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000836	ORPHA:91347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000853	ORPHA:91347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002925	ORPHA:91347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0012503	ORPHA:91347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0012505	ORPHA:91347	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000026	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000044	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000134	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000135	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000140	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000529	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000771	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000802	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000858	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000868	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000938	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000939	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000975	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000980	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0001337	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0001824	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0001962	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002013	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002017	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002315	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002615	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002920	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0003388	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0008240	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0011362	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0011734	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0011735	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0011748	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0011782	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0012041	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0012378	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0030018	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0100639	ORPHA:91347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000508	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000618	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000651	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000789	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000822	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000823	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000837	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000845	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0000870	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0001117	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0001250	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0001635	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0001698	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002321	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0002900	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0004308	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0005115	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0006824	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0006897	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0007011	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0007942	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0008153	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0008247	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0012246	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0012377	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0030517	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0030521	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91347	TSH-secreting pituitary adenoma		HP:0030588	ORPHA:91347	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000010	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000142	ORPHA:1334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000153	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000159	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000478	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000504	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000682	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000790	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000951	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000962	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000988	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0000989	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0001231	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0001250	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0001597	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0001821	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0002105	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0002205	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0002715	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0002719	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0004306	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0004370	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0008388	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0008872	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0010783	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0012115	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0012735	ORPHA:1334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0030016	ORPHA:1334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0100825	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0200034	ORPHA:1334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1334	Chronic mucocutaneous candidiasis		HP:0200042	ORPHA:1334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0000083	ORPHA:2668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0000093	ORPHA:2668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0000407	ORPHA:2668	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0000843	ORPHA:2668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0001903	ORPHA:2668	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0003072	ORPHA:2668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0012062	ORPHA:2668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2668	Nephropathy-deafness-hyperparathyroidism syndrome		HP:0100820	ORPHA:2668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000508	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000618	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000651	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000863	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000870	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000871	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000873	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0001117	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0001250	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002050	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002321	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0006824	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0006897	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0007011	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0007942	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0012246	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0012377	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0030088	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0030517	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0030998	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002893	ORPHA:91349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000026	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000044	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000134	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000135	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000140	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000529	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000802	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000824	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000830	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000837	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000846	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000858	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000868	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000980	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002013	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002017	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002315	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002615	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0002920	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0003388	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0008240	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0008245	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0008993	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0010972	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0011362	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0011734	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0011735	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0011748	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0011804	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0012041	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0012378	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0012503	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0030018	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0030521	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0040075	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0100639	ORPHA:91349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91349	Non-functioning pituitary adenoma		HP:0000053	ORPHA:91349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0000079	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0000126	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0000193	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0000405	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0001172	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0008071	ORPHA:2669	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0009611	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0010055	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2669	Nephrosis-deafness-urinary tract-digital malformations syndrome		HP:0010097	ORPHA:2669	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0006725	ORPHA:1333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0001738	ORPHA:1333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0001824	ORPHA:1333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002027	ORPHA:1333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002039	ORPHA:1333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0003418	ORPHA:1333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0004396	ORPHA:1333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0012432	ORPHA:1333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0000952	ORPHA:1333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002716	ORPHA:1333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0004389	ORPHA:1333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0005249	ORPHA:1333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0012334	ORPHA:1333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0000819	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0001433	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002017	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002254	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002861	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002896	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0002910	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0003002	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0003003	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0025318	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1333	Familial pancreatic carcinoma		HP:0100592	ORPHA:1333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0040171	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0046504	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0100639	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0001250	ORPHA:95702	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0001824	ORPHA:95702	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0002225	ORPHA:95702	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0003154	ORPHA:95702	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0000953	ORPHA:95702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0008163	ORPHA:95702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0000044	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0000798	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0000823	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0001531	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0002013	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0002014	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0002018	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0002153	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0002321	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0002902	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0008186	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0008207	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0008734	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0012378	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95702	X-linked adrenal hypoplasia congenita		HP:0030344	ORPHA:95702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0002865	ORPHA:1332	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0003528	ORPHA:1332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0005994	ORPHA:1332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0000975	ORPHA:1332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0002014	ORPHA:1332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0002015	ORPHA:1332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0002716	ORPHA:1332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0001618	ORPHA:1332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0001824	ORPHA:1332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0002666	ORPHA:1332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0008200	ORPHA:1332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0010622	ORPHA:1332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0030146	ORPHA:1332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1332	Medullary thyroid carcinoma		HP:0100526	ORPHA:1332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0011759	ORPHA:91348	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000140	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000505	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000789	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000802	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000830	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0001123	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0012378	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0030018	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0030088	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0040086	ORPHA:91348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000138	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000141	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000238	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000798	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000823	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000824	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000837	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000863	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000871	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000938	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0000939	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0001541	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0002050	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0002315	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0002625	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0002750	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0008236	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0008245	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0008675	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0009888	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0011748	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0012246	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91348	Functioning gonadotropic adenoma		HP:0100829	ORPHA:91348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0011577	ORPHA:1330	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001653	ORPHA:1330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001962	ORPHA:1330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0002205	ORPHA:1330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0002875	ORPHA:1330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0009020	ORPHA:1330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0030148	ORPHA:1330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001279	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001636	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001643	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001647	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001650	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001680	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001681	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001692	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001702	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0001719	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0002326	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0004383	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0004749	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0006689	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0010772	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0011565	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0030853	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1330	Partial atrioventricular septal defect		HP:0031298	ORPHA:1330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0100627	ORPHA:95706	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000028	ORPHA:95706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0012435	ORPHA:95706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000048	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000054	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000175	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000716	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000739	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000776	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0000818	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0001539	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0002023	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0002032	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0008226	ORPHA:95706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0001518	ORPHA:95706	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95706	Non-syndromic posterior hypospadias		HP:0008722	ORPHA:95706	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95707	Idiopathic isolated micropenis		HP:0000054	ORPHA:95707	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:95707	Idiopathic isolated micropenis	NOT	HP:0000047	ORPHA:95707	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:95707	Idiopathic isolated micropenis	NOT	HP:0000062	ORPHA:95707	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000316	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000337	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000407	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000426	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0005280	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0009836	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0009882	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0010059	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0010109	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0010185	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0011304	ORPHA:2662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000256	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000286	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000327	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000508	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0001609	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0002263	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0004209	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0010624	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0010804	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0030680	ORPHA:2662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0000708	ORPHA:2662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0004322	ORPHA:2662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2662	Keipert syndrome		HP:0100543	ORPHA:2662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2663	Nathalie syndrome		HP:0000407	ORPHA:2663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2663	Nathalie syndrome		HP:0000518	ORPHA:2663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2663	Nathalie syndrome		HP:0004322	ORPHA:2663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2663	Nathalie syndrome		HP:0011675	ORPHA:2663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1338	Heart defect-tongue hamartoma-polysyndactyly syndrome		HP:0000028	ORPHA:1338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1338	Heart defect-tongue hamartoma-polysyndactyly syndrome		HP:0001233	ORPHA:1338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1338	Heart defect-tongue hamartoma-polysyndactyly syndrome		HP:0001643	ORPHA:1338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1338	Heart defect-tongue hamartoma-polysyndactyly syndrome		HP:0001682	ORPHA:1338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1338	Heart defect-tongue hamartoma-polysyndactyly syndrome		HP:0011802	ORPHA:1338	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1338	Heart defect-tongue hamartoma-polysyndactyly syndrome		HP:0100835	ORPHA:1338	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1336	Hyperkeratosis-hyperpigmentation syndrome		HP:0000962	ORPHA:1336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1336	Hyperkeratosis-hyperpigmentation syndrome		HP:0000992	ORPHA:1336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1336	Hyperkeratosis-hyperpigmentation syndrome		HP:0007400	ORPHA:1336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1336	Hyperkeratosis-hyperpigmentation syndrome		HP:0007565	ORPHA:1336	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1336	Hyperkeratosis-hyperpigmentation syndrome		HP:0200034	ORPHA:1336	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0001511	ORPHA:86822	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0001561	ORPHA:86822	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0000252	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0000282	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0001302	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0001321	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0001338	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0001339	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0001762	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0002089	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0002134	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0002365	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0002804	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0003330	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0003405	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0006827	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0006872	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0007190	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0008178	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0009882	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0010049	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0010655	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86822	Lissencephaly type 3-metacarpal bone dysplasia syndrome		HP:0012697	ORPHA:86822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000750	ORPHA:500055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001263	ORPHA:500055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001999	ORPHA:500055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0410263	ORPHA:500055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000135	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000565	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000718	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000729	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001249	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001250	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001252	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001288	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001319	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001508	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002020	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002079	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002099	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0004322	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0007018	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0007082	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0008872	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0012450	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0012762	ORPHA:500055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000028	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000054	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000238	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000248	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000252	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000365	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000486	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000545	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0000639	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001344	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001357	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001371	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001385	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001558	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0001773	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002028	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002033	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002119	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002360	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002650	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0002808	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0004482	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0006970	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0008770	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0010535	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0012166	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0025160	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0025502	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0100710	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500055	Hao-Fountain syndrome due to 16p13.2 microdeletion		HP:0200055	ORPHA:500055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0011356	ORPHA:293812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0010783	ORPHA:293812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0025474	ORPHA:293812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0020172	ORPHA:293812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0000953	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0000155	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0011354	ORPHA:293812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0010280	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0007473	ORPHA:293812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0003341	ORPHA:293812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0410323	ORPHA:293812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0008066	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0200041	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0032565	ORPHA:293812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0032156	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0001945	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0025143	ORPHA:293812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293812	Fixed drug eruption		HP:0012378	ORPHA:293812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0003366	ORPHA:86820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0031520	ORPHA:86820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0007311	ORPHA:86820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0008800	ORPHA:86820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0008812	ORPHA:86820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0008843	ORPHA:86820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0030838	ORPHA:86820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0031058	ORPHA:86820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86820	Familial avascular necrosis of femoral head		HP:0100559	ORPHA:86820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000365	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000473	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000716	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000739	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0001251	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0001300	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0001348	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0001761	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0001762	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002063	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002066	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002067	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002071	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002174	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002360	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002395	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002451	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0003487	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0003785	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0004373	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0008297	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0012378	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0045007	ORPHA:98808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000666	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000722	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000821	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0000822	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0001370	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002166	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002601	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0002650	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0005876	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia		HP:0007325	ORPHA:98808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98808	Autosomal dominant dopa-responsive dystonia	NOT	HP:0001249	ORPHA:98808	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000160	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000189	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000324	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000347	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000348	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000486	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000508	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0000520	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0001387	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0002162	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0002650	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0002683	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0003272	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0003307	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0003422	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0004322	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0004422	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0005048	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0006101	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0100490	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0100555	ORPHA:1323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1323	Camptodactyly-joint contractures-facial skeletal defects syndrome		HP:0001511	ORPHA:1323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0001332	ORPHA:98809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0002072	ORPHA:98809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0002305	ORPHA:98809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0004305	ORPHA:98809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0100660	ORPHA:98809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0011157	ORPHA:98809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0001250	ORPHA:98809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0002076	ORPHA:98809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98809	Paroxysmal kinesigenic dyskinesia		HP:0002356	ORPHA:98809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000239	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000256	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000270	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000303	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000316	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000337	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000400	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000453	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000682	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000944	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001156	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001249	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001263	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001328	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001582	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0002684	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0002750	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0003103	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0003510	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0004279	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0004437	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0005465	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001382	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0006101	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0006660	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0007495	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0008065	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0009773	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0011001	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0011002	ORPHA:2658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000023	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000028	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000036	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000039	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000047	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000154	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000614	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001167	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0003070	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0005916	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0010628	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0012471	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0100541	ORPHA:2658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000135	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000175	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000176	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000193	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0000238	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001252	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001274	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001331	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001376	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001804	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0001812	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0002650	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0002705	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0002808	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2658	Lenz-Majewski hyperostotic dwarfism		HP:0003241	ORPHA:2658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0000707	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0001332	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002059	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002500	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002758	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003445	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003458	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0005108	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0100285	ORPHA:1320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0000234	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0001300	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003236	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003444	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0006959	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0007354	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0012647	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0100022	ORPHA:1320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002134	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002145	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002486	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002511	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0002715	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003396	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003398	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003416	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0003737	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0007361	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0012486	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0012548	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0030113	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0030197	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0100315	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1320	Idiopathic camptocormia		HP:0100614	ORPHA:1320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0000643	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0000726	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0002015	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0001618	ORPHA:98805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0007325	ORPHA:98805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0012049	ORPHA:98805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0000182	ORPHA:98805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0000194	ORPHA:98805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0000473	ORPHA:98805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0001288	ORPHA:98805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0003782	ORPHA:98805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0009938	ORPHA:98805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0002075	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0002098	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0002751	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0004305	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98805	Primary dystonia, DYT4 type		HP:0007351	ORPHA:98805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0001332	ORPHA:98806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0007325	ORPHA:98806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0001260	ORPHA:98806	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0000473	ORPHA:98806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0000643	ORPHA:98806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0012049	ORPHA:98806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0012179	ORPHA:98806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0031008	ORPHA:98806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98806	Primary dystonia, DYT6 type		HP:0002451	ORPHA:98806	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0004373	ORPHA:98807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0001609	ORPHA:98807	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0007325	ORPHA:98807	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0000473	ORPHA:98807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0000733	ORPHA:98807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0001304	ORPHA:98807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0002172	ORPHA:98807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0004305	ORPHA:98807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0001332	ORPHA:98807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0002451	ORPHA:98807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0006961	ORPHA:98807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0012179	ORPHA:98807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0002174	ORPHA:98807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98807	Primary dystonia, DYT13 type		HP:0002345	ORPHA:98807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002034	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002583	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002597	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0003549	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0004296	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0005224	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0025015	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0100590	ORPHA:70475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002019	ORPHA:70475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002027	ORPHA:70475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0100279	ORPHA:70475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0500005	ORPHA:70475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0005214	ORPHA:70475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0012089	ORPHA:70475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0012702	ORPHA:70475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0100806	ORPHA:70475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002014	ORPHA:70475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002573	ORPHA:70475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70475	Radiation proctitis		HP:0002607	ORPHA:70475	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000010	ORPHA:93110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0010957	ORPHA:93110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0012622	ORPHA:93110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000076	ORPHA:93110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000126	ORPHA:93110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000020	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000083	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000822	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0003774	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0008718	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0008897	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0010677	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0010945	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0012330	ORPHA:93110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000016	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000278	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0000316	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0001254	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0001562	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0005105	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0008661	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93110	Posterior urethral valve		HP:0100518	ORPHA:93110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000481	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000502	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000591	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000613	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0001096	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0007879	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0009926	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0011496	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0011859	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0012393	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0025337	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0030953	ORPHA:70476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000622	ORPHA:70476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000643	ORPHA:70476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0025350	ORPHA:70476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0033841	ORPHA:70476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0034804	ORPHA:70476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0100699	ORPHA:70476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000498	ORPHA:70476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0000563	ORPHA:70476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0007663	ORPHA:70476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0012804	ORPHA:70476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70476	Vernal keratoconjunctivitis		HP:0032107	ORPHA:70476	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000003	ORPHA:93111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000047	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000083	ORPHA:93111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000085	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000104	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000303	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000365	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000813	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000819	ORPHA:93111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000821	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0000952	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001249	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001263	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001369	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001397	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001919	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001959	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001994	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0002021	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0002149	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0002910	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0005584	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0001382	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0009715	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0012092	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0012093	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0012873	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0100800	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93111	HNF1B-related autosomal dominant tubulointerstitial kidney disease		HP:0100820	ORPHA:93111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001674	ORPHA:1329	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0010445	ORPHA:1329	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001508	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0003115	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0005120	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0012382	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0025447	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0030950	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0030973	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0031650	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0031664	ORPHA:1329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0000961	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0000975	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001635	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001640	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001649	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001667	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001708	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0002240	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0002789	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0006532	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0011968	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0030828	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0030864	ORPHA:1329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001254	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001678	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0004890	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0011712	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0030830	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0030848	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0031595	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0031658	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0100786	ORPHA:1329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1329	Complete atrioventricular septal defect		HP:0001999	ORPHA:1329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000925	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000929	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000940	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002652	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002653	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002818	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002823	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0031095	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0004326	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0005464	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0005791	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0006501	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0012544	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0040071	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0100774	ORPHA:1328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001324	ORPHA:1328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001376	ORPHA:1328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002515	ORPHA:1328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002992	ORPHA:1328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0003202	ORPHA:1328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0100255	ORPHA:1328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000016	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000135	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000365	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000501	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000520	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000648	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000670	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000684	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000763	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0000823	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001251	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001533	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001639	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001744	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001763	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001882	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001903	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0001999	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002007	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002039	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002167	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002240	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002644	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002650	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002673	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002808	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0002857	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0003307	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0003565	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0007552	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0007807	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0008872	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1328	Camurati-Engelmann disease		HP:0010628	ORPHA:1328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000160	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000218	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000248	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000252	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000275	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000276	ORPHA:1327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000286	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000303	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000358	ORPHA:1327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000463	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000482	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000506	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000581	ORPHA:1327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000664	ORPHA:1327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000689	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000767	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000768	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000774	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000960	ORPHA:1327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0000995	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001156	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001249	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001250	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001263	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001511	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001770	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001822	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0001831	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0002414	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0002553	ORPHA:1327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0002714	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0002750	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0002967	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0003196	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0003312	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0003691	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0004322	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0005280	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0006292	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0008551	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0009882	ORPHA:1327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0009891	ORPHA:1327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0009907	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0010807	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0011800	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0012368	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1327	Camptodactyly syndrome, Guadalajara type 1		HP:0100490	ORPHA:1327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001250	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001251	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001257	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001324	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001397	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001410	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001639	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002072	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002344	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002376	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002465	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002540	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0003688	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0007183	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0009830	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0010841	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0011203	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0100022	ORPHA:70472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0000248	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001290	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001627	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001635	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001999	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002015	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002020	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002060	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002310	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002870	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002878	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0005599	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0007325	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0010536	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0011471	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0012243	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0100660	ORPHA:70472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001252	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001263	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001508	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0001942	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002151	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002401	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0002490	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0003128	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0008347	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70472	Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type		HP:0012379	ORPHA:70472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0000066	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0000252	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0000767	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0001511	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0001762	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0001885	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0002827	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0003065	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0004322	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0004634	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0005643	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0011917	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1326	Camptodactyly syndrome, Guadalajara type 2		HP:0100490	ORPHA:1326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000256	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000774	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000926	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000944	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001252	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001582	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002089	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002187	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002652	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002983	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0005280	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0008873	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0010306	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0010880	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0012368	ORPHA:2655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000365	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000520	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001156	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001511	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002007	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002119	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002282	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0011800	ORPHA:2655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000077	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000238	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000369	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000494	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0000956	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001250	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001385	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001387	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001561	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001631	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001643	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002093	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002676	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002808	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0002867	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0001382	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0030680	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2655	Thanatophoric dysplasia		HP:0100781	ORPHA:2655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1325	Camptodactyly-taurinuria syndrome		HP:0001836	ORPHA:1325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1325	Camptodactyly-taurinuria syndrome		HP:0003166	ORPHA:1325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1325	Camptodactyly-taurinuria syndrome		HP:0003355	ORPHA:1325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1325	Camptodactyly-taurinuria syndrome		HP:0100490	ORPHA:1325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000083	ORPHA:86818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000093	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000233	ORPHA:86818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000272	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000365	ORPHA:86818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000463	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000486	ORPHA:86818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000494	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000545	ORPHA:86818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0000944	ORPHA:86818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0001182	ORPHA:86818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0001252	ORPHA:86818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0001595	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0001643	ORPHA:86818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0001646	ORPHA:86818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0002907	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0004445	ORPHA:86818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0005280	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0010864	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0011069	ORPHA:86818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0012471	ORPHA:86818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86818	Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome		HP:0100820	ORPHA:86818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0001249	ORPHA:86814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0001336	ORPHA:86814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0002197	ORPHA:86814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0002315	ORPHA:86814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0002353	ORPHA:86814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0002378	ORPHA:86814	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0007359	ORPHA:86814	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86814	Familial adult myoclonic epilepsy		HP:0100576	ORPHA:86814	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0001824	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0002024	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0002039	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0002721	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0003202	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0004326	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0004395	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90081	AIDS wasting syndrome		HP:0500012	ORPHA:90081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0000253	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0000486	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0000733	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001252	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001270	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001288	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0011968	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0100660	ORPHA:561854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0000505	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0000729	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0000749	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0000817	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001257	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001266	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001273	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001332	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001336	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001344	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002019	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002020	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002069	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002310	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002360	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002487	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0003763	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0003781	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0004322	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0004325	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0007359	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0008850	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0011344	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0012448	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0012469	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0030215	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0100022	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0100543	ORPHA:561854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0012760	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001274	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0001302	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002079	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002376	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002465	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002540	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002650	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002751	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002795	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0007766	ORPHA:561854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0002133	ORPHA:561854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:561854	FOXG1 syndrome		HP:0012171	ORPHA:561854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0000969	ORPHA:86816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0003073	ORPHA:86816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0001518	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0001622	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0003075	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0003077	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0003124	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0005413	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0009125	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0010702	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0010741	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0012378	ORPHA:86816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0000282	ORPHA:86816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0001513	ORPHA:86816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0001562	ORPHA:86816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0002783	ORPHA:86816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0005268	ORPHA:86816	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0011342	ORPHA:86816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86816	Congenital analbuminemia		HP:0030851	ORPHA:86816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0001288	ORPHA:86812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003551	ORPHA:86812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0000252	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0000750	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0001249	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0002515	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0002938	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003236	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003391	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003557	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003560	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003687	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003701	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003733	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0008981	ORPHA:86812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0000729	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0001319	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0001638	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0001712	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0002027	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0002094	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0002098	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0002650	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003198	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003306	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003325	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003388	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003700	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0003803	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0010794	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0012735	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86812	POMT1-related limb-girdle muscular dystrophy R11		HP:0031108	ORPHA:86812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293807	Ketamine-induced biliary dilatation		HP:0000738	ORPHA:293807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293807	Ketamine-induced biliary dilatation		HP:0002027	ORPHA:293807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293807	Ketamine-induced biliary dilatation		HP:0012440	ORPHA:293807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293807	Ketamine-induced biliary dilatation		HP:0100518	ORPHA:293807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1313	Infantile choroidocerebral calcification syndrome		HP:0000486	ORPHA:1313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1313	Infantile choroidocerebral calcification syndrome		HP:0001250	ORPHA:1313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1313	Infantile choroidocerebral calcification syndrome		HP:0001347	ORPHA:1313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1313	Infantile choroidocerebral calcification syndrome		HP:0002514	ORPHA:1313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1313	Infantile choroidocerebral calcification syndrome		HP:0010864	ORPHA:1313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000023	ORPHA:2645	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000028	ORPHA:2645	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000316	ORPHA:2645	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000347	ORPHA:2645	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000411	ORPHA:2645	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000453	ORPHA:2645	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000463	ORPHA:2645	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0000889	ORPHA:2645	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0001156	ORPHA:2645	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0001249	ORPHA:2645	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0001363	ORPHA:2645	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0001531	ORPHA:2645	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0002650	ORPHA:2645	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0002750	ORPHA:2645	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0003312	ORPHA:2645	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0003510	ORPHA:2645	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0006283	ORPHA:2645	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0008905	ORPHA:2645	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0009804	ORPHA:2645	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2645	Osteoglosphonic dysplasia		HP:0011849	ORPHA:2645	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0100581	ORPHA:93109	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0000010	ORPHA:93109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0000105	ORPHA:93109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0000107	ORPHA:93109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0000126	ORPHA:93109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0000790	ORPHA:93109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0001970	ORPHA:93109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0012211	ORPHA:93109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis		HP:0000787	ORPHA:93109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93109	Congenital megacalycosis	NOT	HP:0006000	ORPHA:93109	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0000324	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0000520	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0000708	ORPHA:1310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0001945	ORPHA:1310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0002093	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0002650	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0004490	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0005731	ORPHA:1310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0005791	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0006465	ORPHA:1310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0008872	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0010702	ORPHA:1310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0100658	ORPHA:1310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1310	Caffey disease		HP:0100963	ORPHA:1310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000003	ORPHA:93108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000009	ORPHA:93108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000091	ORPHA:93108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0008678	ORPHA:93108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0011130	ORPHA:93108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0012575	ORPHA:93108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0012622	ORPHA:93108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000010	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000020	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000070	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000072	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000076	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000083	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000105	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000126	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0000822	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0001562	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0002027	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0004722	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0005999	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0012300	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0012330	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0012596	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0030157	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0031500	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0031501	ORPHA:93108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0001586	ORPHA:93108	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93108	Renal dysplasia		HP:0010957	ORPHA:93108	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0001153	ORPHA:1319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0001156	ORPHA:1319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0001231	ORPHA:1319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0001770	ORPHA:1319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0001800	ORPHA:1319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0006101	ORPHA:1319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0009465	ORPHA:1319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0009601	ORPHA:1319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1319	Camptobrachydactyly		HP:0100490	ORPHA:1319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000083	ORPHA:93101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000091	ORPHA:93101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0005563	ORPHA:93101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0011035	ORPHA:93101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0012210	ORPHA:93101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0012622	ORPHA:93101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0030162	ORPHA:93101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000010	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000069	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000076	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000093	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000122	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000125	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000126	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0000822	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0001518	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0001622	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0001944	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0001959	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93101	Renal hypoplasia		HP:0010481	ORPHA:93101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0000003	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0000175	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0000268	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0000476	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0000772	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0001156	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0001522	ORPHA:1318	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0001562	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0001732	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0001737	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0002652	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0002983	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0005562	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0006487	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0007495	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0100760	ORPHA:1318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0000765	ORPHA:1318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0001789	ORPHA:1318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0002240	ORPHA:1318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0002863	ORPHA:1318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0010781	ORPHA:1318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0100569	ORPHA:1318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0000280	ORPHA:1318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0001004	ORPHA:1318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0002242	ORPHA:1318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0008056	ORPHA:1318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1318	Campomelia, Cumming type		HP:0030680	ORPHA:1318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0000252	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0000494	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0000518	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0000772	ORPHA:2643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0001156	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0001249	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0001252	ORPHA:2643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0001511	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0001875	ORPHA:2643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0002119	ORPHA:2643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0002205	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0002714	ORPHA:2643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0002750	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0002850	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0003510	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0004315	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0005930	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2643	Microcephalic primordial dwarfism, Toriello type		HP:0006297	ORPHA:2643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001251	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001257	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001276	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001315	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001612	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0002093	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0002353	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0002514	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0100543	ORPHA:1314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0000252	ORPHA:1314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001250	ORPHA:1314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001508	ORPHA:1314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001561	ORPHA:1314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0001608	ORPHA:1314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0002269	ORPHA:1314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1314	Symmetrical thalamic calcifications		HP:0011675	ORPHA:1314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0002983	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0002992	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0003022	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0003038	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0003042	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0003048	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0003498	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0009465	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0010781	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0040071	ORPHA:2634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0005048	ORPHA:2634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0000486	ORPHA:2634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2634	Mesomelic dwarfism, Reinhardt-Pfeiffer type		HP:0000545	ORPHA:2634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0007099	ORPHA:268882	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002315	ORPHA:268882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002331	ORPHA:268882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0030833	ORPHA:268882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0040010	ORPHA:268882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0000360	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0000639	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0001293	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0001605	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002015	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002066	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002073	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002196	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002321	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002395	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002516	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002650	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002949	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0003396	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0003474	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0004602	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0004608	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0006824	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0007067	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0009591	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0010558	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0010825	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0010826	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0011389	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0012046	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0012534	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0025258	ORPHA:268882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0000020	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0000613	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0000651	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0001324	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0001437	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0002512	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0003487	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0005758	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0008615	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0010536	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0012366	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268882	Arnold-Chiari malformation type I		HP:0030195	ORPHA:268882	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0012735	ORPHA:1302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0032177	ORPHA:1302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0001945	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0001974	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0002039	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0002091	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0002094	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0003565	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0011897	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0012378	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0025179	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0030830	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0031246	ORPHA:1302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0000961	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0001824	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0002105	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0011227	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0030828	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0031994	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0032016	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0100749	ORPHA:1302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0002098	ORPHA:1302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0002107	ORPHA:1302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0002829	ORPHA:1302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0012418	ORPHA:1302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0025421	ORPHA:1302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1302	Cryptogenic organizing pneumonia		HP:0030166	ORPHA:1302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000175	ORPHA:2635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000238	ORPHA:2635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000348	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000358	ORPHA:2635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000518	ORPHA:2635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000772	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000774	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0000944	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0001387	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0002650	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0002652	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0002808	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0002826	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0002983	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0003103	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0003312	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0003336	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0003510	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0004209	ORPHA:2635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0005108	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0005280	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0006703	ORPHA:2635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0008434	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0100490	ORPHA:2635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0100670	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2635	Metatropic dysplasia		HP:0100818	ORPHA:2635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000028	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000046	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000048	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000059	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000062	ORPHA:1300	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000175	ORPHA:1300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000219	ORPHA:1300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000347	ORPHA:1300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000453	ORPHA:1300	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0000772	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0001171	ORPHA:1300	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0001328	ORPHA:1300	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0001387	ORPHA:1300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0001597	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0001770	ORPHA:1300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0002230	ORPHA:1300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0002650	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0006101	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0008288	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0009754	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0009755	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0009756	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0100267	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1300	Autosomal dominant popliteal pterygium syndrome		HP:0100335	ORPHA:1300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000072	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000077	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000079	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000126	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000252	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000269	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000278	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000347	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000358	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000369	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000414	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000448	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000470	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000501	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000520	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000924	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000938	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000939	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000944	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001156	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001167	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001176	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001249	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001250	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001257	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001263	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001276	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001328	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001511	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001596	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0001622	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002063	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002094	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002121	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002133	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002748	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002749	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002750	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002878	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0002983	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0003172	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0003189	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0003312	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0003510	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0003552	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0004279	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0005108	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0005613	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0005916	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0006660	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0007598	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0008070	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0008818	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0009832	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0009836	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0010443	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0010935	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0011097	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0011457	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0045074	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0100530	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0100569	ORPHA:2636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000028	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000175	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000176	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000193	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000268	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000272	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000340	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000474	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0000494	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0004209	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0009912	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2636	Microcephalic osteodysplastic primordial dwarfism types I and III		HP:0012471	ORPHA:2636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000055	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000252	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000278	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000293	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000369	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000407	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000430	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000431	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000448	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000494	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000691	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000826	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000944	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0000958	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001053	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001156	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001249	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001250	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001263	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001297	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001511	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001601	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001611	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001620	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001631	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001643	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001903	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001956	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002079	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002119	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002205	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002213	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002617	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002650	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002750	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002777	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002812	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002866	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0002983	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0003275	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0003498	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0004209	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0001382	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0005930	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0007018	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0007565	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0009804	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0009906	ORPHA:2637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0045025	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0100545	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0100659	ORPHA:2637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2637	Microcephalic osteodysplastic primordial dwarfism type II		HP:0100840	ORPHA:2637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0000446	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0001156	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0001172	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0001376	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0002818	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0002983	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0002992	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0003272	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0004322	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0005048	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0005930	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0006492	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0007598	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0008368	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2639	Fibular aplasia-complex brachydactyly syndrome		HP:0040071	ORPHA:2639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000365	ORPHA:293843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000508	ORPHA:293843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000537	ORPHA:293843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002553	ORPHA:293843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002974	ORPHA:293843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0006394	ORPHA:293843	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000202	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000316	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000494	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000506	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000581	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000593	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0001249	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0001363	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0001540	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002265	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002558	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002650	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002714	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0003298	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0003307	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0008689	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0008897	ORPHA:293843	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000369	ORPHA:293843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0000377	ORPHA:293843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0001537	ORPHA:293843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002825	ORPHA:293843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0002827	ORPHA:293843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0005105	ORPHA:293843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293843	3MC syndrome		HP:0040016	ORPHA:293843	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0000952	ORPHA:90062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001404	ORPHA:90062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002910	ORPHA:90062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0012115	ORPHA:90062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0000712	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0000713	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0000846	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0000978	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001289	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001350	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001873	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001943	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001987	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002013	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002014	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002018	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002329	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002605	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002614	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002615	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002793	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002795	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0003225	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0003256	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0008151	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0008169	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0008321	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0030977	ORPHA:90062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0000716	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0000988	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001250	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001251	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001259	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001298	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001892	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001919	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001941	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001945	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0001948	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002170	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002181	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002239	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002311	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002516	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002625	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0002883	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0007021	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0012417	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0031273	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90062	Acute liver failure		HP:0031844	ORPHA:90062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1309	Medullary sponge kidney		HP:0000787	ORPHA:1309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1309	Medullary sponge kidney		HP:0000790	ORPHA:1309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1309	Medullary sponge kidney		HP:0001528	ORPHA:1309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1309	Medullary sponge kidney		HP:0002150	ORPHA:1309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1309	Medullary sponge kidney		HP:0008341	ORPHA:1309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000028	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000212	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000218	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000243	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000252	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000286	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000319	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000343	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000347	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000358	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000463	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000470	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000582	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001249	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0003196	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0004209	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0004422	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0005280	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0010458	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0100720	ORPHA:1308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000191	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000233	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000486	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000767	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000960	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001250	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001252	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001373	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001376	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001531	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001582	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001883	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0002983	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0003083	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0004322	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0004378	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0007598	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0007601	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0010978	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0030680	ORPHA:1308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000003	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000085	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000175	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0000776	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001161	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001522	ORPHA:1308	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001539	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001561	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0001770	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0002019	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0007370	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0008678	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0010318	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1308	C syndrome		HP:0010720	ORPHA:1308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0000980	ORPHA:90064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0009763	ORPHA:90064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0011121	ORPHA:90064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0012514	ORPHA:90064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0025018	ORPHA:90064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0001974	ORPHA:90064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0003401	ORPHA:90064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0003690	ORPHA:90064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0006937	ORPHA:90064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0030846	ORPHA:90064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0031271	ORPHA:90064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0001297	ORPHA:90064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0001658	ORPHA:90064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0001941	ORPHA:90064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0003470	ORPHA:90064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0004755	ORPHA:90064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90064	Acute peripheral arterial occlusion		HP:0100758	ORPHA:90064	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000308	ORPHA:1307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000327	ORPHA:1307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000358	ORPHA:1307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0002916	ORPHA:1307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0003028	ORPHA:1307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0005916	ORPHA:1307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0012165	ORPHA:1307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000028	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000083	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000089	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000093	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000160	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000218	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000405	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000545	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0002342	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0003019	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0006501	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0009601	ORPHA:1307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000171	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000175	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000256	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000407	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000426	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000639	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0000691	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0001839	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0004322	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0008368	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1307	Distal limb deficiencies-micrognathia syndrome		HP:0040071	ORPHA:1307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0009145	ORPHA:90065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0000822	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001133	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001259	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001342	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002013	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002018	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002315	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002354	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0012250	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0025637	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0100543	ORPHA:90065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0000238	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0000505	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0000821	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001250	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001279	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001635	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001658	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001712	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0001974	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002140	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002344	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002490	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0002637	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0003074	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0003124	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0004302	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0005184	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0006824	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0030955	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0031058	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0031885	ORPHA:90065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90065	Acquired aneurysmal subarachnoid hemorrhage		HP:0040075	ORPHA:90065	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0000112	ORPHA:442582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0000853	ORPHA:442582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0001917	ORPHA:442582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0030843	ORPHA:442582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0031047	ORPHA:442582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0031185	ORPHA:442582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0100292	ORPHA:442582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442582	AH amyloidosis		HP:0009830	ORPHA:442582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000028	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000252	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000286	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000316	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000325	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000543	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000649	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000708	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000713	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000729	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000750	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0001263	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000767	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0010554	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0001249	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0001252	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000964	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0004322	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0002079	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0002119	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0002123	ORPHA:314389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0002521	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0000232	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0002788	ORPHA:314389	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0003236	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0003282	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0003700	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0004691	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0005280	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0001054	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0007328	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0009908	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0011265	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0011343	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0012751	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0030353	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314389	Xq12-q13.3 duplication syndrome		HP:0100739	ORPHA:314389	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0000202	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0000252	ORPHA:1305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0000347	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0000407	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0000463	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0001156	ORPHA:1305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0001249	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0001643	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0001734	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0001743	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0001770	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0001822	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0002032	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0002247	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0003312	ORPHA:1305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0004209	ORPHA:1305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0004322	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0005280	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0000377	ORPHA:1305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0009468	ORPHA:1305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1305	Feingold syndrome		HP:0012745	ORPHA:1305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0000175	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0000233	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0000278	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0000358	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0000396	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0000944	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0002089	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0002101	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0003027	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0003042	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0003272	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0003422	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0005916	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0005930	ORPHA:2631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0006487	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0010781	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2631	Mesomelic dwarfism-cleft palate-camptodactyly syndrome		HP:0100490	ORPHA:2631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0000218	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0001191	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0002983	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0003067	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0003510	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0005026	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0005930	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0006487	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0006492	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0008873	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0009465	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0040071	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2632	Langer mesomelic dysplasia		HP:0100864	ORPHA:2632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001392	ORPHA:1304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000975	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001369	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001744	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001824	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001882	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001903	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001945	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002018	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002039	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002240	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002829	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0003095	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0003237	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0003565	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0011024	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0011227	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012378	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0025155	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0025406	ORPHA:1304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000031	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000099	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000119	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000707	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000716	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000951	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000979	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001508	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001518	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001622	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001873	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001971	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001974	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002011	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002013	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002027	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002090	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002202	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002315	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002716	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002754	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002923	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0003496	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0005086	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0005268	ORPHA:1304	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0005561	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0008843	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0009830	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012252	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012317	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012387	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0025143	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0025245	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0030350	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0032252	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0100326	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0100523	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0100796	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0410008	ORPHA:1304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0000708	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001626	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001646	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001701	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0001894	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002072	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002326	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0002383	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0004418	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012089	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012122	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012424	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0012819	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0025044	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0030250	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0031910	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0032620	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1304	Brucellosis		HP:0100584	ORPHA:1304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000709	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000713	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000725	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000822	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000975	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001649	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001945	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0011499	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0011999	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0100749	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0100754	ORPHA:90068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000093	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001658	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002013	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002018	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002027	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002107	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002113	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002789	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0003236	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0004372	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0005115	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0006803	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0008765	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0012735	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0025421	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0025435	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0030157	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0030828	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0031258	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0100598	ORPHA:90068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000099	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000746	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0000790	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001250	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001259	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001337	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001342	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001657	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001919	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0001970	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002069	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002098	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002105	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002133	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002138	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002140	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002583	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002615	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002647	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0002883	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0003201	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0004305	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0004308	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0005244	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0005521	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0006677	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0007359	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0011106	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0011151	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0025085	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0025420	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90068	Cocaine intoxication		HP:0031368	ORPHA:90068	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0001376	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0002857	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0002974	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0002983	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0002991	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0002992	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0003027	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0003042	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0006501	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0008368	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0008845	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0010781	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0040071	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0100490	ORPHA:2633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0000248	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0000268	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0000486	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0000960	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0001249	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0002650	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0002970	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0003019	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0004209	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0006101	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0007598	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2633	Mesomelic dysplasia, Nievergelt type		HP:0100729	ORPHA:2633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0002094	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0006536	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0011946	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0012418	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0012735	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0030877	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0032341	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0032342	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0032359	ORPHA:1303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0002090	ORPHA:1303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0011947	ORPHA:1303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0031246	ORPHA:1303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0045051	ORPHA:1303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0002110	ORPHA:1303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0002960	ORPHA:1303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1303	Bronchiolitis obliterans		HP:0025179	ORPHA:1303	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0002113	ORPHA:90060	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0001824	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0001903	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0001945	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0002105	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0002960	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0003565	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0012735	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0025179	ORPHA:90060	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0000093	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0000152	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0000707	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0000790	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0000924	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0000951	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0001873	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0001974	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0002094	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0002923	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0003259	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0003453	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0003493	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0003613	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0004887	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0005421	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0012418	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0045042	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0045050	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0100749	ORPHA:90060	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0002091	ORPHA:90060	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0002206	ORPHA:90060	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0006536	ORPHA:90060	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0025174	ORPHA:90060	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90060	Diffuse alveolar hemorrhage		HP:0030950	ORPHA:90060	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0004322	ORPHA:2623	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000219	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000311	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000343	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000405	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000463	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001072	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001156	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001376	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001511	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001561	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001773	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002099	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002750	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0003026	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0003196	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0004279	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0004890	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0006536	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0011428	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0034281	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0034350	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0034392	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0040261	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0410018	ORPHA:2623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000316	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000483	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000540	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000545	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001385	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001601	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001602	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001650	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001653	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0001718	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002091	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002093	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002240	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002777	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002779	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0002870	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0006530	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0006695	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0012185	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0030051	ORPHA:2623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000501	ORPHA:2623	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2623	Geleophysic dysplasia		HP:0000821	ORPHA:2623	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001518	ORPHA:90051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001622	ORPHA:90051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001649	ORPHA:90051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0010978	ORPHA:90051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0040187	ORPHA:90051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0000980	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001319	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001875	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001942	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001945	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001974	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002045	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002094	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002579	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0003270	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0004325	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0011227	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0011410	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0012719	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0030783	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0031602	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0032169	ORPHA:90051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0000236	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0000952	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0000961	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0000967	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0000969	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0000979	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001250	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001265	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001287	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001410	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001662	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001744	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001873	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001892	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0001903	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002013	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002014	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002240	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002615	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002686	ORPHA:90051	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0002795	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0004387	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0004713	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0005968	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0030863	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0100520	ORPHA:90051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0011880	ORPHA:90051	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0020101	ORPHA:90051	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90051	Sepsis in premature infants		HP:0031696	ORPHA:90051	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0012163	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0100775	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000965	ORPHA:91387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0003549	ORPHA:91387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0200146	ORPHA:91387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000525	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000822	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001640	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001659	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001677	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002875	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0004933	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0005162	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0012499	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0012763	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0100749	ORPHA:91387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000023	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000098	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000278	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000316	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000766	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0000978	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001166	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001297	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001643	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001647	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0001763	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002105	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002107	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002138	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002140	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002326	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002616	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002647	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002650	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002686	ORPHA:91387	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0002705	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0004944	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0004950	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0004959	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0005112	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91387	Familial thoracic aortic aneurysm and aortic dissection		HP:0011106	ORPHA:91387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0100561	ORPHA:90058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0001257	ORPHA:90058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0002315	ORPHA:90058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0002839	ORPHA:90058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0003474	ORPHA:90058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0010549	ORPHA:90058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0012332	ORPHA:90058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0000016	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0002590	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0002953	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0003072	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0003396	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0007185	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0012533	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90058	Spinal cord injury		HP:0012534	ORPHA:90058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000020	ORPHA:404448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000729	ORPHA:404448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0012760	ORPHA:404448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000750	ORPHA:404448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001263	ORPHA:404448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002167	ORPHA:404448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000722	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000739	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001167	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001382	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002020	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002591	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0007018	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0008947	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0011343	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0011344	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0012443	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0012450	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0025160	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0200136	ORPHA:404448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000010	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000179	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000219	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000243	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000319	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000369	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000411	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000483	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000486	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000540	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000718	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000954	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001357	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001488	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001597	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001780	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001852	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001956	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002013	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002059	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002079	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002119	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002360	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002376	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002788	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002835	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0004322	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0005216	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0006288	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0006610	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0007042	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0008551	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0009890	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0010442	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0011342	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0011471	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0030680	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0100704	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0200006	ORPHA:404448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000023	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000028	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000248	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000252	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000577	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000612	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000637	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0000646	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001007	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001118	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001156	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001250	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001276	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0001537	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002098	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0002209	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0004691	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0005280	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0008935	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0010055	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404448	ADNP syndrome		HP:0011304	ORPHA:404448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0000272	ORPHA:1885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0000303	ORPHA:1885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0000505	ORPHA:1885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0000518	ORPHA:1885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0000639	ORPHA:1885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0000646	ORPHA:1885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0000822	ORPHA:1885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0001083	ORPHA:1885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0001387	ORPHA:1885	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0009918	ORPHA:1885	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1885	Isolated ectopia lentis		HP:0100543	ORPHA:1885	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0000407	ORPHA:1883	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0000670	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0000962	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0001166	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0002208	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0002299	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0002650	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0002808	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0004322	ORPHA:1883	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0007529	ORPHA:1883	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0008070	ORPHA:1883	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0009183	ORPHA:1883	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0100490	ORPHA:1883	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1883	Ectodermal dysplasia-sensorineural deafness syndrome		HP:0100543	ORPHA:1883	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0000708	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0000821	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0000966	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0001596	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0001810	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0002205	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0002209	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0002213	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0002750	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0004322	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0008391	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0012265	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0045075	ORPHA:1882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0000632	ORPHA:1882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1882	Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome		HP:0000995	ORPHA:1882	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001622	ORPHA:1880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001631	ORPHA:1880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0002093	ORPHA:1880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0010316	ORPHA:1880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0011575	ORPHA:1880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0012378	ORPHA:1880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0030680	ORPHA:1880	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0000961	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001643	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001671	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001962	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0005110	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0005180	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0011675	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0011712	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0031667	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0100749	ORPHA:1880	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001635	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001645	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0002094	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0002637	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0004306	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0004420	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0010741	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0012418	ORPHA:1880	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001297	ORPHA:1880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1880	Ebstein malformation of the tricuspid valve		HP:0001658	ORPHA:1880	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000238	ORPHA:53271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000248	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000256	ORPHA:53271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000272	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000316	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000407	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000508	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0000520	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0001034	ORPHA:53271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0001053	ORPHA:53271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0001263	ORPHA:53271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0001357	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0001773	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0002516	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0002705	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0004279	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0004440	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0005599	ORPHA:53271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0008368	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0009702	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53271	Muenke syndrome		HP:0010579	ORPHA:53271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0000407	ORPHA:314404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0030050	ORPHA:314404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0000648	ORPHA:314404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0003287	ORPHA:314404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0000020	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0000518	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0000639	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0000716	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0000763	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0001251	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0001257	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0001268	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0001272	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0001347	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002059	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002200	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002322	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002346	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002354	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002476	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002500	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002529	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0002921	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0003487	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0003550	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0007082	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0007366	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314404	Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		HP:0009830	ORPHA:314404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000256	ORPHA:404443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0011407	ORPHA:404443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000708	ORPHA:404443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001513	ORPHA:404443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002342	ORPHA:404443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002751	ORPHA:404443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0008947	ORPHA:404443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000028	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000280	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000311	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000574	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000739	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001250	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001256	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001382	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001566	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001631	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001831	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002119	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002308	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002376	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0008094	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0010864	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0045025	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0100753	ORPHA:404443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000303	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000316	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0000718	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001537	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001643	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0001653	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002000	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002002	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0002616	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0003508	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0005180	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0007302	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0011688	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0012324	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404443	Tatton-Brown-Rahman syndrome		HP:0100634	ORPHA:404443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0001248	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0001762	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0002093	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0002827	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0002999	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0003042	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0031095	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0003417	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0004976	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0006408	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0008417	ORPHA:56305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0000218	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0000347	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0001188	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0001263	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0001561	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0002990	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0003049	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0003862	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0003902	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0003974	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0005257	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0005619	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0005736	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0005905	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0006384	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56305	Atelosteogenesis type III		HP:0008755	ORPHA:56305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0009826	ORPHA:56304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000175	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000470	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000773	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000774	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001156	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001193	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001230	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001234	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001591	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001602	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001776	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001840	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001852	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001999	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0002089	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0002786	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0002857	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0003097	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0003423	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0004991	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0005257	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0006009	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0006375	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0006385	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0008110	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0008752	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0008905	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0009803	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0009824	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0010049	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0012385	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0012427	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0100694	ORPHA:56304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000219	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000286	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000316	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000343	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000347	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000369	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0000506	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001357	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001538	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0001561	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0002947	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0002983	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0002987	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0004664	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0008434	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0011800	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0012810	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0100337	ORPHA:56304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56304	Atelosteogenesis type II		HP:0003042	ORPHA:56304	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0012074	ORPHA:454718	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0000622	ORPHA:454718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0001284	ORPHA:454718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0007695	ORPHA:454718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0009916	ORPHA:454718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0011499	ORPHA:454718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0000540	ORPHA:454718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0000613	ORPHA:454718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0001278	ORPHA:454718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0012803	ORPHA:454718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454718	Holmes-Adie syndrome		HP:0034315	ORPHA:454718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0000726	ORPHA:412066	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0000719	ORPHA:412066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002145	ORPHA:412066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002333	ORPHA:412066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002354	ORPHA:412066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0012757	ORPHA:412066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0000736	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0000739	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0000741	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0001300	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002067	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002172	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002362	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002463	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002506	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0002527	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0003552	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0007311	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0010794	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0030216	ORPHA:412066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments		HP:0006892	ORPHA:412066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments	NOT	HP:0002503	ORPHA:412066	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:412066	PRKAR1B-related neurodegenerative dementia with intermediate filaments	NOT	HP:0007373	ORPHA:412066	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000750	ORPHA:412069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001249	ORPHA:412069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001252	ORPHA:412069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001263	ORPHA:412069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001270	ORPHA:412069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000486	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000925	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001250	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001251	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001273	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001382	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001508	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001999	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0002474	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0002781	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0002870	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0011477	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0011968	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0012443	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0031936	ORPHA:412069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000316	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000347	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000365	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000369	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000385	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000411	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000490	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000494	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000565	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000582	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0000717	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001363	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0001601	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0002079	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0002353	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0002650	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0002779	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0004887	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0005280	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0006951	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0009909	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0012448	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0025267	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0025573	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412069	AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome		HP:0100704	ORPHA:412069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0000505	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0000551	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0000613	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0000639	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0000648	ORPHA:1873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0000682	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0000705	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0007703	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1873	Jalili syndrome		HP:0011073	ORPHA:1873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000613	ORPHA:1872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000662	ORPHA:1872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0007703	ORPHA:1872	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000529	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000543	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000551	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000603	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0001105	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0007641	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0007737	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0007843	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0030466	ORPHA:1872	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000505	ORPHA:1872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0000639	ORPHA:1872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1872	Cone rod dystrophy		HP:0012508	ORPHA:1872	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1871	Progressive cone dystrophy		HP:0000505	ORPHA:1871	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1871	Progressive cone dystrophy		HP:0000512	ORPHA:1871	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1871	Progressive cone dystrophy		HP:0000551	ORPHA:1871	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1871	Progressive cone dystrophy		HP:0000613	ORPHA:1871	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1871	Progressive cone dystrophy		HP:0007703	ORPHA:1871	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0003785	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0012153	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0012447	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0012450	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0025455	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0025457	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0025458	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000580	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000648	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001488	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0011496	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0030001	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0040209	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000297	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000559	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000657	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001265	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001332	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001336	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001374	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001382	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001385	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001413	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001414	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001744	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001771	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001929	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002072	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002119	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002121	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002171	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002205	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002240	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002305	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002345	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002421	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002650	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002673	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002750	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002909	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0003086	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0003121	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0003447	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0003834	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0004349	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0005484	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0005543	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0008151	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0010819	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0010821	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0011167	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0011900	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0011954	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0012340	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0012448	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0012469	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0020037	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0025336	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0025401	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0030194	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0030906	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0031008	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0031051	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0031146	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0031162	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0100899	ORPHA:404454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000543	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000548	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000577	ORPHA:404454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002059	ORPHA:404454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002487	ORPHA:404454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0007141	ORPHA:404454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000522	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0000633	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001249	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001263	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001266	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001272	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001344	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001508	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0001518	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002123	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002187	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002353	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002376	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002465	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002540	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002659	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002870	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0002910	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404454	Alacrimia-choreoathetosis-liver dysfunction syndrome		HP:0003563	ORPHA:404454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1879	Melorheostosis with osteopoikilosis		HP:0000822	ORPHA:1879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1879	Melorheostosis with osteopoikilosis		HP:0000951	ORPHA:1879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1879	Melorheostosis with osteopoikilosis		HP:0001012	ORPHA:1879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1879	Melorheostosis with osteopoikilosis		HP:0001482	ORPHA:1879	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1879	Melorheostosis with osteopoikilosis		HP:0003103	ORPHA:1879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1879	Melorheostosis with osteopoikilosis		HP:0010001	ORPHA:1879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1879	Melorheostosis with osteopoikilosis		HP:0010739	ORPHA:1879	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0000098	ORPHA:1878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0000298	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0001288	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0002515	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0003198	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0003236	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0003457	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0003557	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1878	TRIM32-related limb-girdle muscular dystrophy R8		HP:0008994	ORPHA:1878	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0001633	ORPHA:1876	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0002024	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0002578	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0003198	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0003202	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0003270	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0004326	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0004389	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0011024	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0000508	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0000544	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0004295	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1876	Oculogastrointestinal muscular dystrophy		HP:0005203	ORPHA:1876	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0000135	ORPHA:1875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0000137	ORPHA:1875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0000298	ORPHA:1875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0000486	ORPHA:1875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0000508	ORPHA:1875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0000518	ORPHA:1875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0001252	ORPHA:1875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0001288	ORPHA:1875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0002808	ORPHA:1875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0002967	ORPHA:1875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0003560	ORPHA:1875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0001382	ORPHA:1875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0006610	ORPHA:1875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1875	Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome		HP:0008734	ORPHA:1875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0000028	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0000608	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0000750	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0001159	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0001260	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0001270	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0001285	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0001332	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0002120	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0002200	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0002307	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0002342	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0003396	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0007030	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0008780	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0011506	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0012469	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404451	FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome		HP:0031936	ORPHA:404451	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0001738	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0001824	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0002027	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0002570	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0003270	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0004905	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0011892	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0012378	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0100512	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0100513	ORPHA:309031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0000939	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0001097	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0001510	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0001891	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0002014	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0002748	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0002749	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0012047	ORPHA:309031	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0000707	ORPHA:309031	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0000969	ORPHA:309031	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309031	Pancreatic triacylglycerol lipase deficiency		HP:0002583	ORPHA:309031	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0000405	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0000457	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0000774	ORPHA:1861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0000944	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0001249	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0001250	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0001251	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0001252	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0001263	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0001334	ORPHA:1861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0002878	ORPHA:1861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0004322	ORPHA:1861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1861	Thoracic dysplasia-hydrocephalus syndrome		HP:0009826	ORPHA:1861	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000077	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000238	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000256	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000260	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000365	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000520	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000774	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000926	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000944	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000946	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0000956	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001156	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001171	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001250	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001252	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001387	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001561	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001582	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001631	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0001643	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002007	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002093	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002119	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002187	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002282	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002652	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002676	ORPHA:1860	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002808	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002980	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0002983	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0003097	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0003185	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0005280	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0006487	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0006703	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0007392	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0008909	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0010880	ORPHA:1860	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0012368	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1860	Thanatophoric dysplasia type 1		HP:0100781	ORPHA:1860	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0000252	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0000953	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0001063	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0001182	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0001256	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0001596	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0002090	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0004322	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0005590	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0007957	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0008066	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0008404	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0009381	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0011361	ORPHA:1867	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0000028	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0000262	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0000518	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0001510	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0001627	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0003241	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0008734	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0030148	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1867	Hereditary bullous dystrophy, macular type		HP:0500262	ORPHA:1867	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000470	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000774	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001376	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001762	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002879	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002979	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002983	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003026	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003510	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0005268	ORPHA:1865	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0009826	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0012368	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0040064	ORPHA:1865	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000028	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000119	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000160	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000175	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000238	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000252	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000347	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000358	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000369	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000431	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000519	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000520	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000773	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0000946	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001007	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001059	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001195	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001371	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001627	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0001789	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002084	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002089	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0002093	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003173	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0003175	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0005622	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0032548	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1865	Dyssegmental dysplasia, Silverman-Handmaker type		HP:0100759	ORPHA:1865	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1852	X-linked retinal dysplasia		HP:0000486	ORPHA:1852	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1852	X-linked retinal dysplasia		HP:0000505	ORPHA:1852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1852	X-linked retinal dysplasia		HP:0000639	ORPHA:1852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1852	X-linked retinal dysplasia		HP:0007703	ORPHA:1852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1852	X-linked retinal dysplasia		HP:0007973	ORPHA:1852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1852	X-linked retinal dysplasia		HP:0008046	ORPHA:1852	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0001970	ORPHA:91500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0007813	ORPHA:91500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0025466	ORPHA:91500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0032589	ORPHA:91500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0032590	ORPHA:91500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0032637	ORPHA:91500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0001085	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0001824	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0001945	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0002907	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0003259	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0012122	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0012123	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0012213	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0012378	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0012595	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0025337	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0100586	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0200026	ORPHA:91500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0000505	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0000518	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0000613	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0000988	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0001895	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0001897	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0001994	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0002027	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0002039	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0002829	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0003237	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0003326	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0003355	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0003565	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0004918	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0007902	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0007906	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0008682	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0010702	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0011227	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0011484	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0011505	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0011506	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0012121	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0012124	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0025188	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0030157	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0031616	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0031851	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0040049	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0100532	ORPHA:91500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0007703	ORPHA:91500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0007777	ORPHA:91500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91500	Tubulointerstitial nephritis and uveitis syndrome		HP:0011525	ORPHA:91500	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000003	ORPHA:1851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0002643	ORPHA:1851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0001622	ORPHA:1851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0003270	ORPHA:1851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0031500	ORPHA:1851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000028	ORPHA:1851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000076	ORPHA:1851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000105	ORPHA:1851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000122	ORPHA:1851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0001562	ORPHA:1851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000070	ORPHA:1851	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000074	ORPHA:1851	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000085	ORPHA:1851	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0000822	ORPHA:1851	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1851	Multicystic dysplastic kidney		HP:0030735	ORPHA:1851	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0000164	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0000303	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0000689	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0001156	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0001249	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0001250	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0001385	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0002353	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0002650	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0002652	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0002808	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0002866	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0003212	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0004322	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1858	Skeletal dysplasia-epilepsy-short stature syndrome		HP:0009882	ORPHA:1858	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0000175	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0000365	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0000545	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0001384	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0003022	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0003071	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0003498	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0005106	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0005863	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0008788	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0010582	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0045060	ORPHA:1856	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0000518	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0000541	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0000926	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0001377	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0001385	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0001883	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0003300	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0003365	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0008812	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0010055	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1856	Spondyloperipheral dysplasia-short ulna syndrome		HP:0010743	ORPHA:1856	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000926	ORPHA:1855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0003493	ORPHA:1855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0100255	ORPHA:1855	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001257	ORPHA:1855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002960	ORPHA:1855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0004322	ORPHA:1855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0012622	ORPHA:1855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0020151	ORPHA:1855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0410263	ORPHA:1855	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000093	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000684	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000689	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000707	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000790	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000822	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000946	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001249	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001263	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001270	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001369	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001890	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001973	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002072	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002119	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002315	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002514	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002518	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002633	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002719	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002725	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002979	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0003326	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0003521	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0005681	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0009826	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0009882	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0012115	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0012514	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0030038	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0030047	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0030880	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0032252	ORPHA:1855	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000768	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000821	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000824	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0000988	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001045	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001250	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0001876	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002090	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0002808	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1855	Spondyloenchondrodysplasia		HP:0011800	ORPHA:1855	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0012286	ORPHA:54595	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002514	ORPHA:54595	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0010576	ORPHA:54595	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0011750	ORPHA:54595	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0012505	ORPHA:54595	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0040075	ORPHA:54595	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000044	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000135	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000863	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000870	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001085	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001262	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001513	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002017	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002315	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002360	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0007924	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0007987	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0008245	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0011734	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0030521	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0030588	ORPHA:54595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000238	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000365	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000648	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000823	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001510	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002516	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002591	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002637	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002659	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0003508	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0005978	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0010535	ORPHA:54595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0000708	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001117	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001249	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001250	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001259	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001263	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0001658	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002321	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0002719	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0008897	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0010939	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54595	Craniopharyngioma		HP:0430000	ORPHA:54595	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000252	ORPHA:404473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0001249	ORPHA:404473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0001257	ORPHA:404473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0001270	ORPHA:404473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0001999	ORPHA:404473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0002465	ORPHA:404473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0008936	ORPHA:404473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000478	ORPHA:404473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000708	ORPHA:404473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0002376	ORPHA:404473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0011451	ORPHA:404473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000219	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000319	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000343	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000430	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000455	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000486	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000540	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000545	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000718	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000729	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0002079	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0002119	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0002144	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0002188	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0002360	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0003396	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0009765	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0025160	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0100716	ORPHA:404473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0000365	ORPHA:404473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:404473	Intellectual disability-peripheral spasticity-exudative vitreoretinopathy syndrome		HP:0001250	ORPHA:404473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000044	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000252	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000668	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000670	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000771	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000823	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000824	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0000953	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0001249	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0001596	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0002333	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0002750	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0002751	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0002828	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0004322	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0006480	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0007373	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0007481	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0009487	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0010627	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0011735	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0030353	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0031074	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0040171	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0100578	ORPHA:157954	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0003700	ORPHA:157954	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0008202	ORPHA:157954	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157954	ANE syndrome		HP:0008245	ORPHA:157954	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0000009	ORPHA:391487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001510	ORPHA:391487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002242	ORPHA:391487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002728	ORPHA:391487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002750	ORPHA:391487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002788	ORPHA:391487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0004322	ORPHA:391487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0000818	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0000823	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0000832	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0000938	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0000964	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001433	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001888	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001890	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001920	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002014	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002110	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002719	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002721	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002958	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0004387	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0004944	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0005353	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0010976	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0011123	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0011473	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0012163	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0040160	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0100646	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0100651	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0100817	ORPHA:391487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001635	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001655	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001873	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001904	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0001973	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002092	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002383	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0002724	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0003613	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0004966	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0011459	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0012115	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0012182	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome		HP:0030355	ORPHA:391487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391487	STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome	NOT	HP:0005403	ORPHA:391487	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001970	ORPHA:449395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0003237	ORPHA:449395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0032300	ORPHA:449395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0000083	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0000093	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0000790	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001919	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0002923	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0003259	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0003493	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0004431	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0005421	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0012622	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0032298	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0032616	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0045042	ORPHA:449395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0000024	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0000105	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0000620	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001082	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001287	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001410	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001679	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001701	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001733	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001824	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0001880	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0002027	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0002088	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0002102	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0002716	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0002840	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0003212	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0005200	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0006000	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0006515	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0011109	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0011123	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0011747	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0012089	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0012378	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0012578	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0012592	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0012593	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0025633	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0030991	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0031032	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0031093	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0031281	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0031549	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0045026	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0100016	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0100577	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0100646	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0500006	ORPHA:449395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0000126	ORPHA:449395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0010741	ORPHA:449395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease		HP:0011227	ORPHA:449395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449395	IgG4-related kidney disease	NOT	HP:0100586	ORPHA:449395	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000008	ORPHA:1839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000014	ORPHA:1839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000119	ORPHA:1839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000212	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000221	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000518	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000613	ORPHA:1839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000639	ORPHA:1839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000790	ORPHA:1839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0000962	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0001131	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0001596	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0002205	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0002206	ORPHA:1839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0002213	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0002575	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0008070	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1839	Hereditary mucoepithelial dysplasia		HP:0012732	ORPHA:1839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0000290	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0000473	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0000483	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0000486	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0000646	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0002007	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0004484	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0011225	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:3000030	ORPHA:620102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0000565	ORPHA:620102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0000577	ORPHA:620102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0012803	ORPHA:620102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0030001	ORPHA:620102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:620102	Non-syndromic unicoronal craniosynostosis		HP:0001085	ORPHA:620102	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217266	BNAR syndrome		HP:0011803	ORPHA:217266	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:217266	BNAR syndrome		HP:0000200	ORPHA:217266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217266	BNAR syndrome		HP:0001545	ORPHA:217266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217266	BNAR syndrome		HP:0002025	ORPHA:217266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217266	BNAR syndrome		HP:0010322	ORPHA:217266	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217266	BNAR syndrome		HP:0000104	ORPHA:217266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217266	BNAR syndrome		HP:0012252	ORPHA:217266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0000104	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0000286	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0000316	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0000369	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0000457	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0001562	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0001958	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0002089	ORPHA:1848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0001563	ORPHA:1848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0002242	ORPHA:1848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0002575	ORPHA:1848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0005107	ORPHA:1848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0030680	ORPHA:1848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0100589	ORPHA:1848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0000008	ORPHA:1848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0000175	ORPHA:1848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0010497	ORPHA:1848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1848	Renal agenesis, bilateral		HP:0100335	ORPHA:1848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0000828	ORPHA:140286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0000121	ORPHA:140286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0000829	ORPHA:140286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0002135	ORPHA:140286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0002901	ORPHA:140286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0002905	ORPHA:140286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0012378	ORPHA:140286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0031817	ORPHA:140286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0000716	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0000739	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0001250	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0002150	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0002380	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0002748	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0002749	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0003394	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0007302	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0007787	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0011675	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0025425	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0031006	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0031990	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0033630	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:0033748	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:4000007	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140286	Secondary hypoparathyroidism due to impaired parathormon secretion		HP:6000919	ORPHA:140286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0000707	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0002721	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0002921	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0004302	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0007305	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0031392	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0100706	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0100707	ORPHA:217260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0000505	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0001260	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0001268	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0002066	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0002167	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0002315	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0003474	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0003690	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0004374	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0005415	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0010549	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0100543	ORPHA:217260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0000639	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0000751	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0001123	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0001250	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0001300	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0002321	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0002381	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0004377	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0012246	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0025479	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0030516	ORPHA:217260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0000651	ORPHA:217260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0001287	ORPHA:217260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0001310	ORPHA:217260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217260	Progressive multifocal leukoencephalopathy		HP:0003401	ORPHA:217260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000773	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000774	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001824	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002093	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002652	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002823	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002983	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0008890	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0008905	ORPHA:1842	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000348	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000364	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000457	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000463	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000470	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0000940	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001172	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001252	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001373	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001591	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002007	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001382	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0005930	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0009811	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0012368	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0030680	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0100255	ORPHA:1842	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001155	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001508	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001631	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001639	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001643	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001883	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0001903	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002014	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002017	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002205	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0002240	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0005989	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1842	Bone dysplasia, lethal Holmgren type		HP:0100790	ORPHA:1842	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0000822	ORPHA:231580	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0003351	ORPHA:231580	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0011740	ORPHA:231580	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0002900	ORPHA:231580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0003081	ORPHA:231580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0008221	ORPHA:231580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0200114	ORPHA:231580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0000360	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0000421	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0001324	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0001959	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0001962	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0002018	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0002315	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231580	Primary unilateral adrenal hyperplasia		HP:0003394	ORPHA:231580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0000020	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0000708	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0001250	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0001257	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0001332	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0001371	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002071	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002072	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002120	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002136	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002167	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002300	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002340	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002361	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002457	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0002607	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0005327	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0007076	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0007240	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0007256	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0007308	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157946	Huntington disease-like 3		HP:0100543	ORPHA:157946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0006532	ORPHA:454750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0008872	ORPHA:454750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0030842	ORPHA:454750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0033362	ORPHA:454750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0001508	ORPHA:454750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0002020	ORPHA:454750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0002098	ORPHA:454750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0002788	ORPHA:454750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0003270	ORPHA:454750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454750	Isolated tracheoesophageal fistula		HP:0200048	ORPHA:454750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0001406	ORPHA:69663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0011848	ORPHA:69663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0001081	ORPHA:69663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0002910	ORPHA:69663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0025502	ORPHA:69663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0030948	ORPHA:69663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0000822	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0001082	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0001402	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0001513	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0001733	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0002896	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0003124	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0005230	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0030151	ORPHA:69663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0000819	ORPHA:69663	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0002613	ORPHA:69663	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0030991	ORPHA:69663	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69663	Low phospholipid-associated cholelithiasis		HP:0100523	ORPHA:69663	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002072	ORPHA:157941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000708	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000716	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000726	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000746	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001260	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001288	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002066	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002119	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0004305	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0100543	ORPHA:157941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000298	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000496	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000514	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000570	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000617	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000639	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000711	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0000750	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001250	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001272	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001290	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001310	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001350	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0001824	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002067	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002120	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002134	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002171	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002311	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002312	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002353	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002354	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002359	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002375	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002457	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0002533	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0003043	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0006801	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0006961	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0007010	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0008003	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0011446	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157941	Huntington disease-like 1		HP:0040201	ORPHA:157941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000648	ORPHA:543470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000750	ORPHA:543470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001263	ORPHA:543470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001508	ORPHA:543470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002194	ORPHA:543470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0010862	ORPHA:543470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000505	ORPHA:543470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001251	ORPHA:543470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001252	ORPHA:543470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001257	ORPHA:543470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002376	ORPHA:543470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002465	ORPHA:543470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0012087	ORPHA:543470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000062	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000252	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000518	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000603	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000618	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0000639	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001250	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001272	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001273	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001276	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001320	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0001622	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002066	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002079	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002134	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002353	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0002506	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0007333	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0008665	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0008936	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0012430	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0012448	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0012697	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0012794	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0100022	ORPHA:543470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome		HP:0100602	ORPHA:543470	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0000989	ORPHA:69665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0012202	ORPHA:69665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0002910	ORPHA:69665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0025031	ORPHA:69665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0100785	ORPHA:69665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0000716	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0002643	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0002904	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0003155	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0012420	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0012689	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0011117	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0030900	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0031248	ORPHA:69665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0100602	ORPHA:69665	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0000821	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0000952	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0001082	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0001337	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0001518	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0001541	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0001622	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0001732	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0002027	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy		HP:0012164	ORPHA:69665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy	NOT	HP:0000988	ORPHA:69665	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69665	Intrahepatic cholestasis of pregnancy	NOT	HP:0002960	ORPHA:69665	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000093	ORPHA:1830	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000097	ORPHA:1830	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000112	ORPHA:1830	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001511	ORPHA:1830	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0003368	ORPHA:1830	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0004322	ORPHA:1830	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0031409	ORPHA:1830	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000455	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000691	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000707	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000822	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000926	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001003	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001034	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001250	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001263	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001297	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001510	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001622	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001875	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001888	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001903	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001999	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002315	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002621	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002637	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002655	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002719	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002926	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002938	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0003077	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0003182	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0003270	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0003300	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0003521	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0005352	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0011840	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0008784	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0008839	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0012593	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0410373	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0410377	ORPHA:1830	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000470	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0000668	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001260	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001269	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001324	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001508	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001518	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001635	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001873	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002092	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002133	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002140	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002301	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002326	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002381	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002907	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0003774	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0004931	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0005280	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0006344	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0006813	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0007957	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0012579	ORPHA:1830	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001298	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0001733	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002242	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002376	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0002960	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0005523	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0005528	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1830	Schimke immuno-osseous dysplasia		HP:0012539	ORPHA:1830	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000708	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000736	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0001250	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0001289	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002354	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0012229	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0032264	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0032266	ORPHA:217253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000738	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000739	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000746	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0001945	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002013	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002014	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002315	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0004305	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0011289	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0012226	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0012332	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0100660	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0100754	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0100785	ORPHA:217253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000709	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000713	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000716	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0000733	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0001266	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0001278	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0001332	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0001336	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002063	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002072	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002133	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002179	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002197	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002300	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002310	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002371	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0002463	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0003781	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0007359	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0008763	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0010553	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0012173	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0012333	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:5200321	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0031258	ORPHA:217253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0003006	ORPHA:217253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0012189	ORPHA:217253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0100013	ORPHA:217253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0100521	ORPHA:217253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0100526	ORPHA:217253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:217253	NMDA receptor encephalitis		HP:0100616	ORPHA:217253	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000218	ORPHA:168624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000243	ORPHA:168624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000256	ORPHA:168624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000268	ORPHA:168624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000303	ORPHA:168624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000316	ORPHA:168624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000348	ORPHA:168624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0000582	ORPHA:168624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0001256	ORPHA:168624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0001770	ORPHA:168624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0002119	ORPHA:168624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0010059	ORPHA:168624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0010807	ORPHA:168624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168624	Familial scaphocephaly syndrome, McGillivray type		HP:0011800	ORPHA:168624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0000944	ORPHA:1837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0002750	ORPHA:1837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0003272	ORPHA:1837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0006501	ORPHA:1837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0040071	ORPHA:1837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0002991	ORPHA:1837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0003312	ORPHA:1837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0004322	ORPHA:1837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0005916	ORPHA:1837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0000164	ORPHA:1837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0000457	ORPHA:1837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0000691	ORPHA:1837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0000787	ORPHA:1837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0001608	ORPHA:1837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1837	Metaphyseal chondrodysplasia, Rosenberg type		HP:0006482	ORPHA:1837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0002750	ORPHA:168621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0008829	ORPHA:168621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0008835	ORPHA:168621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0001974	ORPHA:168621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0002515	ORPHA:168621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0003565	ORPHA:168621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0008800	ORPHA:168621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0012514	ORPHA:168621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0031955	ORPHA:168621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0001374	ORPHA:168621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0001945	ORPHA:168621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0008812	ORPHA:168621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168621	Dysplasia of head of femur, Meyer type		HP:0030812	ORPHA:168621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0000772	ORPHA:1836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0001883	ORPHA:1836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0002967	ORPHA:1836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0002991	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0003027	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0003028	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0031095	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0003422	ORPHA:1836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0004209	ORPHA:1836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0004322	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0005009	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0005048	ORPHA:1836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0008368	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0009465	ORPHA:1836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1836	Mesomelic dysplasia, Kantaputra type		HP:0100490	ORPHA:1836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0000750	ORPHA:404499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0001260	ORPHA:404499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0001265	ORPHA:404499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0002066	ORPHA:404499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0002070	ORPHA:404499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0002194	ORPHA:404499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0001152	ORPHA:404499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0001249	ORPHA:404499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0001250	ORPHA:404499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0000639	ORPHA:404499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404499	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency		HP:0002172	ORPHA:404499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000008	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000069	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000078	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000079	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000107	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000126	ORPHA:1834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000212	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000238	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000316	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000324	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000347	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000384	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000470	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000707	ORPHA:1834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000772	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000776	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000921	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0000924	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0001140	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0001392	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0001539	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0001562	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0001622	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0001743	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002019	ORPHA:1834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002020	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002023	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002120	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002242	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002575	ORPHA:1834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002644	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002650	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0002815	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0003312	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0003422	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0004322	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0006703	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0008551	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0008678	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0012718	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0012732	ORPHA:1834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1834	Axial mesodermal dysplasia spectrum		HP:0100542	ORPHA:1834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0007020	ORPHA:466722	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002061	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0010549	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002395	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0012407	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0003487	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0007210	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002505	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0003800	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0001263	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0000278	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0000675	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0000486	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0000508	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0008936	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002080	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0001260	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002421	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0001250	ORPHA:466722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0001344	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0005216	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002068	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002882	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002751	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0008872	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0000020	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002067	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0001332	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0008110	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0001385	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0001336	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0008689	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0000011	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0025488	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002376	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0100785	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466722	Autosomal recessive spastic paraplegia type 77		HP:0002268	ORPHA:466722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404493	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency		HP:0001249	ORPHA:404493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404493	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency		HP:0001250	ORPHA:404493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404493	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency		HP:0001999	ORPHA:404493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404493	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency		HP:0001251	ORPHA:404493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404493	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency		HP:0000248	ORPHA:404493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404493	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency		HP:0001290	ORPHA:404493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000239	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000252	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000270	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000278	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000347	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000358	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000369	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000457	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000463	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000470	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0009099	ORPHA:1832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000169	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000212	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0000520	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0001511	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0002094	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0002098	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0002878	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0003196	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1832	Osteosclerotic bone dysplasia		HP:0009939	ORPHA:1832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0000366	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0000499	ORPHA:1818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0000668	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0000995	ORPHA:1818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0008070	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0002231	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0006482	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0006709	ORPHA:1818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0007521	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0008388	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0100578	ORPHA:1818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1818	Ectodermal dysplasia, trichoodontoonychial type		HP:0100840	ORPHA:1818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0000774	ORPHA:157973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001252	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001263	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001288	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001371	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001376	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001522	ORPHA:157973	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001558	ORPHA:157973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001635	ORPHA:157973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001883	ORPHA:157973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0002093	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0002421	ORPHA:157973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0003198	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0003202	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0003306	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0003307	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0003327	ORPHA:157973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0003457	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0004326	ORPHA:157973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0001382	ORPHA:157973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0011675	ORPHA:157973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157973	Congenital muscular dystrophy due to LMNA mutation		HP:0011968	ORPHA:157973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000239	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000248	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000316	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000455	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000456	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000506	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0001249	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0001263	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0001274	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0001762	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0001841	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0002056	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0002084	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0002435	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0006866	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0008388	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0009099	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0009928	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0011803	ORPHA:1827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000161	ORPHA:1827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0002119	ORPHA:1827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0002190	ORPHA:1827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0040326	ORPHA:1827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000028	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000154	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000508	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000545	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0001250	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0002690	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0002781	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0003065	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0005772	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0006951	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0010627	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0040075	ORPHA:1827	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0000501	ORPHA:1827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1827	Acromelic frontonasal dysplasia		HP:0025247	ORPHA:1827	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000316	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000336	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000347	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000365	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000431	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000494	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001999	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0002650	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0002652	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0009473	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0009803	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0011304	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0100807	ORPHA:1826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000126	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000280	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000293	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000405	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000407	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000941	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001220	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001239	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001607	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001627	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0002694	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0002949	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0002987	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0002996	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0003016	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0003083	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0006000	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0006070	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0006248	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0008081	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0008661	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0009487	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0009650	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0009882	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0010049	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0010501	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0010505	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0010562	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0010743	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0100490	ORPHA:1826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000175	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000193	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000410	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000481	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000483	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000646	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000677	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000912	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0000954	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001249	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001363	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001510	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0001761	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0002308	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0003298	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0006006	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0006383	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0008952	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1826	Frontometaphyseal dysplasia		HP:0009004	ORPHA:1826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000154	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000286	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000316	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000324	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000343	ORPHA:1825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000407	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000431	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000463	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000508	ORPHA:1825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000708	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0000823	ORPHA:1825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0001053	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0001172	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0001249	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0001250	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0002002	ORPHA:1825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0002650	ORPHA:1825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0002750	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0003019	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0004322	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0005280	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0006101	ORPHA:1825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0007477	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0009623	ORPHA:1825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1825	Epiphyseal dysplasia-hearing loss-dysmorphism syndrome		HP:0100542	ORPHA:1825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0000252	ORPHA:1824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0000483	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0000505	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0000639	ORPHA:1824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0000926	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0001156	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0001249	ORPHA:1824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0001387	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0002656	ORPHA:1824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0002750	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0002812	ORPHA:1824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0002829	ORPHA:1824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0002999	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0003042	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0003083	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0004322	ORPHA:1824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0005930	ORPHA:1824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0007370	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0007703	ORPHA:1824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0010582	ORPHA:1824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1824	Lowry-Wood syndrome		HP:0100643	ORPHA:1824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0001387	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0001763	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0002653	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0002757	ORPHA:1822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0002758	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0002823	ORPHA:1822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0002857	ORPHA:1822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0002970	ORPHA:1822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0003367	ORPHA:1822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0005616	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0005930	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0008368	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0008812	ORPHA:1822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0010582	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0100555	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1822	Dysplasia epiphysealis hemimelica		HP:0100777	ORPHA:1822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53296	Familial cutaneous collagenoma		HP:0001000	ORPHA:53296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53296	Familial cutaneous collagenoma		HP:0001631	ORPHA:53296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53296	Familial cutaneous collagenoma		HP:0001635	ORPHA:53296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53296	Familial cutaneous collagenoma		HP:0001638	ORPHA:53296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53296	Familial cutaneous collagenoma		HP:0001681	ORPHA:53296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53296	Familial cutaneous collagenoma		HP:0200034	ORPHA:53296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53296	Familial cutaneous collagenoma		HP:0200036	ORPHA:53296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0000078	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0000278	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0000365	ORPHA:1809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0000411	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0000561	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0000858	ORPHA:1809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0001231	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0001249	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0002164	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0002209	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0002223	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0002231	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0002552	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0002558	ORPHA:1809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0007477	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0007502	ORPHA:1809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0007565	ORPHA:1809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1809	Hidrotic ectodermal dysplasia, Halal type		HP:0008388	ORPHA:1809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000175	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000286	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000316	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000327	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000349	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000358	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000384	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000486	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000508	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000518	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000568	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000612	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0001156	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0002084	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0002650	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0002738	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0002938	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0004112	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0004423	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0006931	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0007370	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0008591	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0010297	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0011817	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0025247	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0040019	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0100490	ORPHA:391474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0000873	ORPHA:391474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391474	Frontorhiny		HP:0040075	ORPHA:391474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0000653	ORPHA:1808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0001595	ORPHA:1808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0001597	ORPHA:1808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0002209	ORPHA:1808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0002215	ORPHA:1808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0002223	ORPHA:1808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0002225	ORPHA:1808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0008401	ORPHA:1808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0008404	ORPHA:1808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1808	Hidrotic ectodermal dysplasia, Christianson-Fourie type		HP:0011675	ORPHA:1808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000494	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000520	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000592	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000926	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000938	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000944	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000963	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000974	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000978	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001182	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001371	ORPHA:157965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001508	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002652	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003071	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003370	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003393	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0006429	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0008848	ORPHA:157965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0010489	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157965	SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome		HP:0100864	ORPHA:157965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0000286	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0000322	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0000431	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0000457	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0000486	ORPHA:1807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0000494	ORPHA:1807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0000632	ORPHA:1807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0001053	ORPHA:1807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0001582	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0002023	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0002553	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0002714	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0005338	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0007495	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0007565	ORPHA:1807	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0007776	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0008065	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0008070	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0009743	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0010720	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0010751	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0010935	ORPHA:1807	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1807	Focal facial dermal dysplasia type III		HP:0100781	ORPHA:1807	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000164	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000411	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000446	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000482	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000568	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000618	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000647	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0001131	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0001249	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0001999	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0002167	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0004322	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0008070	ORPHA:1806	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000365	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000478	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000504	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000518	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000962	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0000966	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0001000	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0001097	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0001231	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0002205	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0002213	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1806	Ectodermal dysplasia-blindness syndrome		HP:0200042	ORPHA:1806	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000486	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000602	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001298	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001744	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002240	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002653	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002659	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002797	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0010885	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0012378	ORPHA:77261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000726	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000823	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000938	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001250	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001251	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001288	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001510	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001789	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001873	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001876	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001903	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002123	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002750	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0004963	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0007885	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0010702	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0011001	ORPHA:77261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000093	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000164	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000674	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0000790	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001637	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001654	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0001698	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002092	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0002205	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0004322	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0004380	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0004382	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77261	Gaucher disease type 3		HP:0006530	ORPHA:77261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0000486	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0000602	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001257	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001298	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001332	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001744	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002015	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002240	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002793	ORPHA:77260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0000211	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0000605	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0000737	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001250	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001252	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001371	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001873	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001903	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002013	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002094	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002098	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002123	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002179	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002205	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0003656	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0006530	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0007272	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0010307	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0025425	ORPHA:77260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001695	ORPHA:77260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0001790	ORPHA:77260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0002804	ORPHA:77260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0007479	ORPHA:77260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77260	Gaucher disease type 2		HP:0008064	ORPHA:77260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65282	Carvajal syndrome		HP:0001635	ORPHA:65282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65282	Carvajal syndrome		HP:0001644	ORPHA:65282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65282	Carvajal syndrome		HP:0002224	ORPHA:65282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65282	Carvajal syndrome		HP:0005588	ORPHA:65282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0000987	ORPHA:231568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0008066	ORPHA:231568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0001030	ORPHA:231568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0001056	ORPHA:231568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0001810	ORPHA:231568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0008404	ORPHA:231568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0031045	ORPHA:231568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0001075	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0001802	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0001817	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0008390	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0008391	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0031446	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0200041	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231568	Autosomal dominant generalized dystrophic epidermolysis bullosa		HP:0200097	ORPHA:231568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0000158	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0000238	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0000256	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0001161	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0001250	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0001251	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0002017	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0002126	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0002315	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0002516	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0006824	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0012081	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0200034	ORPHA:65285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0010619	ORPHA:65285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0012844	ORPHA:65285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0100031	ORPHA:65285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0100615	ORPHA:65285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65285	Lhermitte-Duclos disease		HP:0200016	ORPHA:65285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000047	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000085	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000164	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000202	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000218	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000232	ORPHA:65286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000252	ORPHA:65286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000256	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000275	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000276	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000322	ORPHA:65286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000324	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000369	ORPHA:65286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000400	ORPHA:65286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000426	ORPHA:65286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000494	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000518	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000568	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000678	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000709	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000716	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000717	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000718	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000739	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000750	ORPHA:65286	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000767	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0000768	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001000	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001182	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001249	ORPHA:65286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001263	ORPHA:65286	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001288	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001508	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001611	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001643	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001682	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0002020	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0002092	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0003196	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0004209	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0001382	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0007018	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0007302	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65286	3q29 microdeletion syndrome		HP:0008416	ORPHA:65286	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome		HP:0000325	ORPHA:65288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome		HP:0000331	ORPHA:65288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome		HP:0000369	ORPHA:65288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome		HP:0000609	ORPHA:65288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome		HP:0000857	ORPHA:65288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome		HP:0001321	ORPHA:65288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome		HP:0100800	ORPHA:65288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001873	ORPHA:91547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001945	ORPHA:91547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0003573	ORPHA:91547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0011227	ORPHA:91547	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0000952	ORPHA:91547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001903	ORPHA:91547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001974	ORPHA:91547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002315	ORPHA:91547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002910	ORPHA:91547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0003326	ORPHA:91547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0025435	ORPHA:91547	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0000079	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001649	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001882	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001892	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0001919	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002013	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002027	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002615	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002829	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0003259	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0012378	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0012735	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0025143	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0031179	ORPHA:91547	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0000421	ORPHA:91547	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0000790	ORPHA:91547	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002014	ORPHA:91547	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0002105	ORPHA:91547	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0008151	ORPHA:91547	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0011897	ORPHA:91547	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91547	Relapsing fever		HP:0011899	ORPHA:91547	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0000554	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0000613	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0000708	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0001287	ORPHA:91546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0001324	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0001369	ORPHA:91546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0001386	ORPHA:91546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0001678	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0001945	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0002017	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0002315	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0002354	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0002383	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0002829	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0003326	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0003401	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0004334	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0006824	ORPHA:91546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0009830	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0011675	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0012378	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0100576	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0100785	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91546	Lyme disease		HP:0200036	ORPHA:91546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000047	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000144	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000457	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000534	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000668	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000684	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000787	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000823	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0000982	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0001249	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0002230	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0004322	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0007400	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0007513	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0008736	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1816	Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome		HP:0009721	ORPHA:1816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000023	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000028	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000175	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000238	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000256	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000278	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000286	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000316	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000369	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000490	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000492	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000494	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000682	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000691	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000767	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000821	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000958	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000963	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0000966	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0001252	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0001274	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0001288	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0001561	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0001852	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0002007	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0002119	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0002213	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0002558	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0002991	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0003196	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0005280	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0007360	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0008736	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0008872	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0010624	ORPHA:1812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0010669	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0010864	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0010978	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1812	Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome		HP:0100840	ORPHA:1812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0000164	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0000670	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0000968	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0001597	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0001799	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0001816	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0006323	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0006337	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1811	Odontomicronychial dysplasia		HP:0008383	ORPHA:1811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0000823	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0000938	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0000939	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001510	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001744	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001971	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002039	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002240	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002653	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002750	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002797	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0003656	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0010885	ORPHA:77259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0000225	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0000978	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001433	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001873	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001876	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001903	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001928	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002027	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0003281	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0031830	ORPHA:77259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0000716	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0000790	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001081	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001409	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001541	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001882	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001892	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002092	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002176	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002756	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002758	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0002953	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0003233	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0004322	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0004975	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0005230	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0006530	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0006775	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0007141	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0010702	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0032640	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0034336	ORPHA:77259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001300	ORPHA:77259	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001394	ORPHA:77259	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0001399	ORPHA:77259	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77259	Gaucher disease type 1		HP:0012223	ORPHA:77259	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0000164	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0000668	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0000963	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0000966	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0002231	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0006323	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0006482	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0008070	ORPHA:1810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0001231	ORPHA:1810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0000457	ORPHA:1810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0000964	ORPHA:1810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0001000	ORPHA:1810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0002047	ORPHA:1810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0011220	ORPHA:1810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1810	Autosomal dominant hypohidrotic ectodermal dysplasia		HP:0012471	ORPHA:1810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000325	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000343	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000347	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000400	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000411	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000414	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000653	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0002007	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0004209	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0004322	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0008070	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0009882	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0010049	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0010579	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0010743	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0011341	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0011910	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0045075	ORPHA:77258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000164	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000218	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0000768	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0001252	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0001808	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0001820	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0002650	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0003307	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0005743	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0011069	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77258	Trichorhinophalangeal syndrome type 1		HP:0100490	ORPHA:77258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000324	ORPHA:794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000348	ORPHA:794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000929	ORPHA:794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001363	ORPHA:794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0004209	ORPHA:794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0004440	ORPHA:794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0006101	ORPHA:794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000189	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000248	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000270	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000294	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000316	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000426	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000444	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000486	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000508	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000643	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001156	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001357	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0003307	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0005280	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0007598	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0007678	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0008551	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000377	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0009738	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0009899	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0010807	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0011386	ORPHA:794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000028	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000175	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000193	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000286	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000327	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000365	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000369	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000405	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000407	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000601	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000646	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0000648	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001199	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001250	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001627	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001822	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0001837	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0002076	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0002315	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0002342	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0002516	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0002650	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0002697	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0002974	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0003312	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0004322	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0005037	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0010084	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0010535	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0010720	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0011304	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:794	Saethre-Chotzen syndrome		HP:0030680	ORPHA:794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0000822	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0001369	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0002015	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0002960	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0003119	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0003236	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0003493	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0003701	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0008997	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0011838	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0025131	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0025142	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0030859	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0030880	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0032169	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0033040	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0033555	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0033560	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0034088	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0034093	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0100296	ORPHA:206572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0000077	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0000819	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0001627	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0001873	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0001882	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0002092	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0002273	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0001288	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0002725	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0002910	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0003549	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0003551	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0004269	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0006530	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0009053	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0009763	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0011121	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0100324	ORPHA:206572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206572	Overlap myositis		HP:0001370	ORPHA:206572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0000765	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0000925	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0000969	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0000988	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0001061	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0001369	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0001581	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002024	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002027	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002028	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002037	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002570	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002653	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002754	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002757	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002797	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002829	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0003765	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0004936	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0005464	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0006824	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0010622	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0100686	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0100769	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0100781	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0100847	ORPHA:793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0200039	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0002633	ORPHA:793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0100749	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:793	SAPHO syndrome		HP:0100774	ORPHA:793	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0002647	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0002650	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0002758	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0003179	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0004268	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0004944	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0005086	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0005116	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0005294	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0012432	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0025487	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000278	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000767	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000768	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001382	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001519	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001627	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001642	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001712	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0003302	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0005110	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0005112	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0008419	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0010886	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0100490	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0100775	ORPHA:284984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000175	ORPHA:284984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000939	ORPHA:284984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001643	ORPHA:284984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome	NOT	HP:0001363	ORPHA:284984	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001763	ORPHA:284984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0002617	ORPHA:284984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0011645	ORPHA:284984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000023	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000139	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000193	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000218	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000272	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000276	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000316	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000348	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000689	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000978	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0000987	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001065	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001166	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001537	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001653	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0001659	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0002076	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284984	Aneurysm-osteoarthritis syndrome		HP:0002315	ORPHA:284984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0000256	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0000293	ORPHA:796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0000365	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0000618	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0001250	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0001251	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0001324	ORPHA:796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0001508	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0001635	ORPHA:796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0001744	ORPHA:796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0002205	ORPHA:796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0002240	ORPHA:796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0002333	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0002652	ORPHA:796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0002808	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0004343	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0007272	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0010729	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:796	Sandhoff disease		HP:0100022	ORPHA:796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001508	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001620	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0002091	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0002194	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0002421	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0002650	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0002828	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0002877	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0003306	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0003327	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0003560	ORPHA:324604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0000218	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001290	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0003700	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0004322	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0004889	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0005991	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0009058	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0030319	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0100295	ORPHA:324604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0000303	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0000308	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001385	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001634	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001635	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001667	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001708	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy		HP:0001763	ORPHA:324604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324604	Classic multiminicore myopathy	NOT	HP:0030091	ORPHA:324604	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0009919	ORPHA:790	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0000486	ORPHA:790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0000501	ORPHA:790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0000520	ORPHA:790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0000555	ORPHA:790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0031615	ORPHA:790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0000554	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0001100	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0001909	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0002665	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0002669	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0002859	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0002861	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0007663	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0007703	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0007862	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0007902	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0011886	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0012372	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0025244	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0025337	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0100243	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0100658	ORPHA:790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0000175	ORPHA:790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0009733	ORPHA:790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0012254	ORPHA:790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:790	Retinoblastoma		HP:0030408	ORPHA:790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000496	ORPHA:792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000501	ORPHA:792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000504	ORPHA:792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000512	ORPHA:792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000529	ORPHA:792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0030502	ORPHA:792	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000493	ORPHA:792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0007722	ORPHA:792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0007902	ORPHA:792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0007984	ORPHA:792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0025158	ORPHA:792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000486	ORPHA:792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000541	ORPHA:792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0000662	ORPHA:792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0030824	ORPHA:792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:792	X-linked retinoschisis		HP:0030825	ORPHA:792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000405	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000407	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000505	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000512	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000546	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000613	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000618	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000639	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000648	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0007675	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0007703	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0007737	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0008046	ORPHA:791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000501	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000543	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000563	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000602	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000662	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000842	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0001105	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0007787	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0007843	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0007994	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0011505	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0012426	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0030466	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0030488	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0030610	ORPHA:791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0000551	ORPHA:791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0007663	ORPHA:791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:791	Retinitis pigmentosa		HP:0030786	ORPHA:791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157997	Benign cephalic histiocytosis		HP:0000988	ORPHA:157997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157997	Benign cephalic histiocytosis		HP:0100727	ORPHA:157997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157997	Benign cephalic histiocytosis		HP:0200034	ORPHA:157997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157997	Benign cephalic histiocytosis		HP:0011123	ORPHA:157997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0025475	ORPHA:157991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0030350	ORPHA:157991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0100727	ORPHA:157991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0040186	ORPHA:157991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0000989	ORPHA:157991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0031901	ORPHA:157991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0032061	ORPHA:157991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0040126	ORPHA:157991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0001909	ORPHA:157991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis		HP:0005585	ORPHA:157991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis	NOT	HP:0002716	ORPHA:157991	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:157991	Generalized eruptive histiocytosis	NOT	HP:0031871	ORPHA:157991	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000028	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000054	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000121	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000175	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000193	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000233	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000252	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000278	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000316	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000358	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000384	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000405	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000463	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000470	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000483	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000486	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000540	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000582	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000592	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000954	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000960	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001100	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001156	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001274	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001290	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001734	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001845	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001864	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0002019	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0002101	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0002162	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0002788	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0002828	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0003196	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0004209	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0004689	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0004704	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0005280	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0005495	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0006801	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0009913	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0010034	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0010864	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0010945	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0011466	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0011918	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0012758	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0030148	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0040018	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0040022	ORPHA:264450	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000126	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000238	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0000633	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001250	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001305	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001636	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0001711	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0003006	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0004794	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0004969	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0005176	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0008609	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0011546	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0011939	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264450	Trisomy 8p syndrome		HP:0100790	ORPHA:264450	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0001945	ORPHA:319251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0003237	ORPHA:319251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0020071	ORPHA:319251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002039	ORPHA:319251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000478	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000573	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000575	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000613	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0001324	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0003496	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0007663	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0025188	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0032118	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0032323	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0200026	ORPHA:319251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000225	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000554	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000738	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000790	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000952	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0000988	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0001269	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0001873	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0001892	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0001903	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0001977	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002248	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002249	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002315	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002321	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002383	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002385	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0002910	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0003418	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0003470	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0003781	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0004372	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0005268	ORPHA:319251	TAS		HP:0040284			C	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0005542	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0012115	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0012229	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0025013	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0031691	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319251	Rift valley fever		HP:0040049	ORPHA:319251	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0000311	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0000470	ORPHA:1803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0000773	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0000774	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0000944	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0001288	ORPHA:1803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0001591	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0002162	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0002644	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0002857	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0002991	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0003042	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0003307	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0005019	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0001382	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0008873	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0009826	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1803	Thoracomelic dysplasia		HP:0012368	ORPHA:1803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0000944	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0001744	ORPHA:1802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0001903	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0002167	ORPHA:1802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0002644	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0002823	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0002992	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0003103	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0003312	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0004493	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0005019	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0006487	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1802	Ghosal hematodiaphyseal dysplasia		HP:0010978	ORPHA:1802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001653	ORPHA:284979	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0002097	ORPHA:284979	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0005180	ORPHA:284979	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000268	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000485	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000768	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000973	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001083	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001166	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001181	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001270	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001371	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001518	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001626	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001634	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001704	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001713	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0002643	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0004970	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0008124	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0008734	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0010511	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0011003	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0011968	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0012418	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0030148	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0100578	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0100625	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0100693	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0100807	ORPHA:284979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000347	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000369	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000431	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000490	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000494	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0000592	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001252	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001265	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0001382	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0002616	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0002705	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0009901	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284979	Neonatal Marfan syndrome		HP:0012771	ORPHA:284979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0000347	ORPHA:1801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0000774	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0000895	ORPHA:1801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0000907	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0000921	ORPHA:1801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0000944	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0001176	ORPHA:1801	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0001252	ORPHA:1801	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0001376	ORPHA:1801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0001387	ORPHA:1801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0002983	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0003180	ORPHA:1801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0003312	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0003498	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0006487	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0010306	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0010561	ORPHA:1801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1801	Kyphomelic dysplasia		HP:0012368	ORPHA:1801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0001007	ORPHA:786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0003154	ORPHA:786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0004319	ORPHA:786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0012030	ORPHA:786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0012378	ORPHA:786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0000822	ORPHA:786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0000876	ORPHA:786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0001061	ORPHA:786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0002900	ORPHA:786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0008221	ORPHA:786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0030087	ORPHA:786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0200114	ORPHA:786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0000062	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0000789	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0000798	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0000826	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0001943	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0002292	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0003118	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0010458	ORPHA:786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:786	Generalized glucocorticoid resistance syndrome		HP:0001297	ORPHA:786	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000347	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000365	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000369	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000403	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000465	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000474	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000475	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000708	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000739	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000758	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000786	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000822	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000869	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000872	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000914	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001328	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001397	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001513	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001531	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001800	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001952	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002162	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002705	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002808	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002857	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002910	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0005113	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0005689	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0006438	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0006456	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0007477	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0009759	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0010044	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0010047	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0010510	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000085	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000086	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000164	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000286	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000476	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000486	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000508	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000545	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000716	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000767	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000842	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000987	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000995	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001004	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001045	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001231	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001385	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001395	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001596	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001631	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001647	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001657	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001658	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001680	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001763	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001812	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001831	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002608	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002611	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002650	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002960	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0003067	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0003186	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0003764	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0004349	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0005603	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0005978	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0007018	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000377	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0009118	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0011307	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0012434	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0100646	ORPHA:99413	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000150	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000471	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001394	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002037	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002613	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002647	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002861	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0004383	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0004386	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0005294	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0008678	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0012758	ORPHA:99413	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000137	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000470	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000823	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000837	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000879	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000938	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000939	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001510	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0001511	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002750	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0002967	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0003492	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0004322	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0006610	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0006709	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0008209	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0008222	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0008897	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0012774	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0040072	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0100625	ORPHA:99413	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000218	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99413	Turner syndrome due to structural X chromosome anomalies		HP:0000278	ORPHA:99413	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0002553	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0002719	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0004209	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0006817	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0007018	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0009832	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0010535	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0030434	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0030680	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0031087	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0100760	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000365	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000508	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000678	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000987	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001250	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001385	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001513	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001561	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001631	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0002308	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0005306	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0005743	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0006101	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0006530	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0010562	ORPHA:783	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000218	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000316	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000369	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000444	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000494	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000506	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000750	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001156	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001249	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001263	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001531	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0004322	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001382	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0008872	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0010059	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0011087	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0011304	ORPHA:783	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000028	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000119	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000164	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000252	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000286	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000347	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000431	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000486	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000501	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000518	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000579	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000589	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000670	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000708	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000729	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000737	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0000739	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001273	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0001627	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0002019	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0002093	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0002098	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:783	Rubinstein-Taybi syndrome		HP:0002230	ORPHA:783	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000593	ORPHA:782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000627	ORPHA:782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0008053	ORPHA:782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000232	ORPHA:782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000365	ORPHA:782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000501	ORPHA:782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0011800	ORPHA:782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0030680	ORPHA:782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000047	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000316	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000327	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000431	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000506	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000668	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000691	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0000864	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0001510	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0001582	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0002025	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0005280	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:782	Axenfeld-Rieger syndrome		HP:0011220	ORPHA:782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000013	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000098	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000786	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000837	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000938	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000939	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0001548	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0002663	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0003117	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0003187	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0003799	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0008187	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0008197	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0008675	ORPHA:785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000842	ORPHA:785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0000956	ORPHA:785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0001061	ORPHA:785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0001677	ORPHA:785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0001952	ORPHA:785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0002574	ORPHA:785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome		HP:0010679	ORPHA:785	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome	NOT	HP:0000834	ORPHA:785	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome	NOT	HP:0030087	ORPHA:785	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:785	Estrogen resistance syndrome	NOT	HP:0100133	ORPHA:785	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0001250	ORPHA:391457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0001263	ORPHA:391457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0001639	ORPHA:391457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0001942	ORPHA:391457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0003128	ORPHA:391457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0012379	ORPHA:391457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0500170	ORPHA:391457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0001392	ORPHA:391457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391457	HSD10 disease, neonatal type		HP:0003256	ORPHA:391457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0032252	ORPHA:781	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0000613	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0000988	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001324	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001744	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001945	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002014	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002017	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002315	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002910	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0003326	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0003565	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0012378	ORPHA:781	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0000716	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0000790	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0000952	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0000979	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001392	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001433	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001511	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001518	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001562	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001622	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001626	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001824	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001873	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001878	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001903	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002039	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002090	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002240	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002360	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002633	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002829	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002922	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002923	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0003262	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0003613	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0010702	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0011227	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0012115	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0012735	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0020136	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0030166	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0033430	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0040186	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0100584	ORPHA:781	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001082	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001287	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001698	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0001701	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002098	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002202	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002383	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002716	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0002754	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0005162	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0006530	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0011034	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0012819	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0025343	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:781	Q fever		HP:0100778	ORPHA:781	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0025238	ORPHA:566943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0001387	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0001288	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0005656	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0010505	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0010741	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0010885	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0012098	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0030871	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0100339	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0100662	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0100925	ORPHA:566943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0001369	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0001763	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0005063	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0005086	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0008110	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0008124	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0032153	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0100535	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566943	Mueller-Weiss syndrome		HP:0100694	ORPHA:566943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001922	ORPHA:565612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0003756	ORPHA:565612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0009058	ORPHA:565612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0012379	ORPHA:565612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0031331	ORPHA:565612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0000819	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001430	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001435	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001638	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001677	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001681	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001962	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0002094	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0002240	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0003077	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0003236	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0005145	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0009805	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0011675	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0032141	ORPHA:565612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0000407	ORPHA:565612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001249	ORPHA:565612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001733	ORPHA:565612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0003805	ORPHA:565612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0011123	ORPHA:565612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0031684	ORPHA:565612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0000478	ORPHA:565612	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy		HP:0001744	ORPHA:565612	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:565612	Primary triglyceride deposit cardiomyovasculopathy	NOT	HP:0008064	ORPHA:565612	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000028	ORPHA:398079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000135	ORPHA:398079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000789	ORPHA:398079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001270	ORPHA:398079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001513	ORPHA:398079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001999	ORPHA:398079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0008947	ORPHA:398079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000044	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000046	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000060	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000064	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000486	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000708	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000729	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000750	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000786	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001249	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001315	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001319	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001328	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001508	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001612	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001773	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0002119	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0002591	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0002650	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0003241	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0008197	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0008734	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0012166	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0012287	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0012506	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0012743	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0012758	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0025160	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0040288	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0200055	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0410263	ORPHA:398079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000054	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000217	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000219	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000446	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000709	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000826	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000938	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0000939	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001010	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001250	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001254	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0001385	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0002205	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0002494	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0002714	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0002870	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0005599	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0005978	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0007874	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0010536	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0010829	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0011787	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0012411	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0012412	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398079	SIM1-related Prader-Willi-like syndrome		HP:0040030	ORPHA:398079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000154	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000356	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000708	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000729	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0001263	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0001270	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0002465	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0008947	ORPHA:313947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000164	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000219	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000414	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000448	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000486	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000527	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000601	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000678	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000817	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0001155	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0001488	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0001760	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0002136	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0002360	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0002311	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0002553	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0004209	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0005274	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0010055	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0011800	ORPHA:313947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000294	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000331	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000483	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000505	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000957	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0001852	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0002013	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0002020	ORPHA:313947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:313947	2q23.1 microduplication syndrome		HP:0000718	ORPHA:313947	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003198	ORPHA:206569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003236	ORPHA:206569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003458	ORPHA:206569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003713	ORPHA:206569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0030057	ORPHA:206569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0030200	ORPHA:206569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0002015	ORPHA:206569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003202	ORPHA:206569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003326	ORPHA:206569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0008994	ORPHA:206569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0033708	ORPHA:206569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0033713	ORPHA:206569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0100614	ORPHA:206569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0001962	ORPHA:206569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0002664	ORPHA:206569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003327	ORPHA:206569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0003691	ORPHA:206569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0006530	ORPHA:206569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0012819	ORPHA:206569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0100749	ORPHA:206569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0000988	ORPHA:206569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0001635	ORPHA:206569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0002829	ORPHA:206569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206569	Immune-mediated necrotizing myopathy		HP:0030880	ORPHA:206569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0000217	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0000952	ORPHA:779	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0000988	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0000989	ORPHA:779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0001097	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0001369	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0001394	ORPHA:779	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0001541	ORPHA:779	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0001945	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0002015	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0002020	ORPHA:779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0002093	ORPHA:779	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0002240	ORPHA:779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0002383	ORPHA:779	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0003326	ORPHA:779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0004295	ORPHA:779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0007400	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0011354	ORPHA:779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0011838	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0012378	ORPHA:779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0100579	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0100585	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0100725	ORPHA:779	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:779	Reynolds syndrome		HP:0200042	ORPHA:779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000053	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000164	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000218	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000248	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000256	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000275	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000322	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000327	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000347	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000348	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000369	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000411	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000426	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000678	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000708	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000709	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000738	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0000767	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001156	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001166	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001249	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001250	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001252	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001519	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001608	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001611	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001631	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0002167	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0002650	ORPHA:776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0001382	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0007018	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0007370	ORPHA:776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0100490	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:776	Lujan-Fryns syndrome		HP:0100753	ORPHA:776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001288	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0003202	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0003763	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0003808	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0030217	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0033850	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0000713	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001082	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001987	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002151	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002360	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002490	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002540	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002650	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0003542	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0008947	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0012332	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0031793	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0500231	ORPHA:778	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0011451	ORPHA:778	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0000253	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0000733	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001263	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001288	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001344	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002376	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002793	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0007064	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0012171	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0025430	ORPHA:778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001250	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001332	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001508	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0001510	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002067	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:778	Rett syndrome		HP:0002353	ORPHA:778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0005930	ORPHA:166002	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0003365	ORPHA:166002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0009826	ORPHA:166002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0012770	ORPHA:166002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0030839	ORPHA:166002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0030973	ORPHA:166002	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0002515	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0002758	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0002812	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0002815	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0002857	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0002970	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0003028	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0003045	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0003946	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0003999	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0004322	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0006055	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0006190	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0009189	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0010631	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0010665	ORPHA:166002	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0001324	ORPHA:166002	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:166002	Multiple epiphyseal dysplasia due to collagen 9 anomaly		HP:0003198	ORPHA:166002	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0000762	ORPHA:206594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001324	ORPHA:206594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0002922	ORPHA:206594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003431	ORPHA:206594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0007377	ORPHA:206594	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001284	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001288	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001974	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001288	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0002359	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003447	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003474	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003551	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003565	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0004302	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0006881	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0007078	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0007141	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0007220	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0007262	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0011096	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0012531	ORPHA:206594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001266	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001337	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0001430	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0002403	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0002460	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0002936	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003237	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003376	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0003448	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0006376	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0006844	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0007230	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0008800	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0010505	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0012078	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0032169	ORPHA:206594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0002086	ORPHA:206594	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0002270	ORPHA:206594	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206594	Subacute inflammatory demyelinating polyneuropathy		HP:0006824	ORPHA:206594	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0000252	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0001263	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0001273	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0001320	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0002363	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0010663	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0012110	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0012502	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0032398	ORPHA:467166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0000486	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0000657	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0001302	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0002119	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0007018	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0012547	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0031882	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0040327	ORPHA:467166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0000256	ORPHA:467166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0001251	ORPHA:467166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0001252	ORPHA:467166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0001488	ORPHA:467166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0002121	ORPHA:467166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0012469	ORPHA:467166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:467166	Tubulinopathy-associated dysgyria		HP:0020214	ORPHA:467166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002059	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002061	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002079	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002151	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002307	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002353	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002509	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002521	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002650	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0003394	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0003487	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0004305	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0005745	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0006956	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0007366	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0007371	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0011448	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0011470	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0012428	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0030051	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0031959	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0000543	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0000750	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0000817	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001273	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001317	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001321	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001344	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001662	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002421	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002490	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002500	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002505	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0007321	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0008763	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0008872	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0008936	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0011344	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0012379	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0030890	ORPHA:565624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0000028	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0000194	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0000252	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0000762	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001250	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001260	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001324	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001347	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001511	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0001998	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002013	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565624	Combined oxidative phosphorylation defect type 39		HP:0002058	ORPHA:565624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0000256	ORPHA:63446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0000767	ORPHA:63446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0000768	ORPHA:63446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0000774	ORPHA:63446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0001792	ORPHA:63446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0001821	ORPHA:63446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0002650	ORPHA:63446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0002652	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0002750	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0002812	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0002869	ORPHA:63446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0002970	ORPHA:63446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0002983	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0003300	ORPHA:63446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0003307	ORPHA:63446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0003367	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0004279	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0004322	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0006059	ORPHA:63446	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0010306	ORPHA:63446	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63446	Acrocapitofemoral dysplasia		HP:0010579	ORPHA:63446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0011473	ORPHA:398063	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002028	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0001824	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002024	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0001935	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0000939	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002910	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0000707	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0011123	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0030057	ORPHA:398063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002853	ORPHA:398063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002901	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0003075	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002917	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002148	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0001891	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0001897	ORPHA:398063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0001972	ORPHA:398063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0010639	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0012052	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0025409	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002027	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0004395	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002829	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0033143	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002243	ORPHA:398063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0003073	ORPHA:398063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398063	Refractory celiac disease		HP:0002665	ORPHA:398063	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0004220	ORPHA:63442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0005819	ORPHA:63442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0005930	ORPHA:63442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0010034	ORPHA:63442	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0000668	ORPHA:63442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0000684	ORPHA:63442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0001385	ORPHA:63442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0004322	ORPHA:63442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0008843	ORPHA:63442	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0002750	ORPHA:63442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:63442	Angel-shaped phalango-epiphyseal dysplasia		HP:0001382	ORPHA:63442	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000028	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000789	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001249	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001270	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001319	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001371	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001999	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002033	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0008947	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0011968	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0012758	ORPHA:398069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000046	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000060	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000064	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000135	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000478	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000486	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000708	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000729	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000750	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000786	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001256	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001315	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001328	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001508	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001558	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001612	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001773	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002020	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002119	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002591	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002650	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002808	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0003241	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0004322	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0004324	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0005968	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0006889	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0008197	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0008734	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0010535	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0012166	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0012287	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0012450	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0012506	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0012743	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0025160	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0040288	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0100543	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0200055	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0410263	ORPHA:398069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000054	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000217	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000219	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000446	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000545	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000565	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000709	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000722	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000826	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000938	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0000939	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001010	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001250	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001254	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001385	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0001631	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002205	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002494	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002714	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0002870	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0005599	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0005978	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0007874	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0010536	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0010829	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0011787	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0012411	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0040030	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398069	Schaaf-Yang syndrome		HP:0100710	ORPHA:398069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206599	Isolated asymptomatic elevation of creatine phosphokinase		HP:0003236	ORPHA:206599	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:206599	Isolated asymptomatic elevation of creatine phosphokinase	NOT	HP:0003198	ORPHA:206599	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:206599	Isolated asymptomatic elevation of creatine phosphokinase	NOT	HP:0008331	ORPHA:206599	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0000952	ORPHA:521219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0001081	ORPHA:521219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0002027	ORPHA:521219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0002904	ORPHA:521219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0003155	ORPHA:521219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0011980	ORPHA:521219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0040319	ORPHA:521219	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0001649	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0001733	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0001945	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0002013	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0002018	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0002039	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0002910	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0003270	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0011848	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0025143	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0410019	ORPHA:521219	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0030154	ORPHA:521219	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:521219	Mirizzi syndrome		HP:0100889	ORPHA:521219	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0012073	ORPHA:391417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000529	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000750	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001250	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001263	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001328	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002342	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002376	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0040155	ORPHA:391417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000365	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000648	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000708	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000729	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000736	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001251	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001260	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001266	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001288	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001336	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0004925	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0006892	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0007042	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0008947	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0012433	ORPHA:391417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000252	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0000639	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001337	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0001347	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002015	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002063	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002119	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002307	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002313	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0002579	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0007030	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0008897	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391417	HSD10 disease		HP:0011470	ORPHA:391417	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0000011	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0000020	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0000708	ORPHA:206583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0000726	ORPHA:206583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0001249	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0001251	ORPHA:206583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0001257	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0001269	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0001288	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0001324	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0001376	ORPHA:206583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0002071	ORPHA:206583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0002839	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0002936	ORPHA:206583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0003457	ORPHA:206583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0007256	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0009830	ORPHA:206583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206583	Adult polyglucosan body disease		HP:0200042	ORPHA:206583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63455	Paraneoplastic pemphigus		HP:0000155	ORPHA:63455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63455	Paraneoplastic pemphigus		HP:0008066	ORPHA:63455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63455	Paraneoplastic pemphigus		HP:0012191	ORPHA:63455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63455	Paraneoplastic pemphigus		HP:0100242	ORPHA:63455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63455	Paraneoplastic pemphigus		HP:0100522	ORPHA:63455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:63455	Paraneoplastic pemphigus		HP:0200041	ORPHA:63455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:63455	Paraneoplastic pemphigus		HP:0200097	ORPHA:63455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0012760	ORPHA:97685	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000736	ORPHA:97685	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001480	ORPHA:97685	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0007565	ORPHA:97685	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000271	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000529	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000708	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000822	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001072	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001328	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001627	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001999	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002076	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002315	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002354	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002360	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002463	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0004562	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0009732	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0009737	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0011442	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0025105	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0100585	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0200034	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0410263	ORPHA:97685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000337	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000486	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000490	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000501	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000520	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000610	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000618	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000729	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000823	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000925	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000935	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000938	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000939	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001034	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001176	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001249	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001250	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001263	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001271	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001297	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001511	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001639	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001642	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001680	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001833	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001920	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002088	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002092	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002650	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002797	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002808	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0003165	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0004322	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0004944	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0007236	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0007359	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0007524	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0007850	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0009733	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0009734	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0010795	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0010796	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0012492	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0012531	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0030692	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0031023	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0032458	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0100008	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0100697	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0100817	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0430022	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:3000062	ORPHA:97685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000316	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000369	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000465	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000494	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0000826	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0001909	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002666	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002859	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002863	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0002979	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0003001	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0003002	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0005280	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0006610	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0100252	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0100723	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:97685	17q11 microdeletion syndrome		HP:0100775	ORPHA:97685	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000337	ORPHA:798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000455	ORPHA:798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002007	ORPHA:798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0003196	ORPHA:798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0011800	ORPHA:798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0012736	ORPHA:798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0012758	ORPHA:798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000078	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000126	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000154	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000158	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000260	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000316	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000329	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000341	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000356	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000369	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000470	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000505	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000520	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000586	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000885	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001250	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001531	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001627	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002079	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002119	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0004554	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0009882	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0011039	ORPHA:798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000168	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000187	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000218	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000278	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000347	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000375	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000452	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000522	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000684	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000765	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000889	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001537	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001545	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001734	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001845	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002089	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002098	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002120	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002190	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002251	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002645	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002694	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002751	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002982	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0003173	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0007099	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0008610	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0008628	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0009792	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0010034	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0010464	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0010557	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0045005	ORPHA:798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000023	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000047	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000054	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000069	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000107	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000280	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000322	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0000787	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001257	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001276	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001601	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0001605	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002015	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002521	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002650	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002667	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002884	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002888	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0002974	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0005349	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0006532	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0009748	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0011097	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0011471	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0011787	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0012324	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0012385	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0025259	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:798	Schinzel-Giedion syndrome		HP:0030736	ORPHA:798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000836	ORPHA:797	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001878	ORPHA:797	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001880	ORPHA:797	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002045	ORPHA:797	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002105	ORPHA:797	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000518	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000618	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000620	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000787	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000873	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000953	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001010	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001097	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001369	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001399	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001409	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001482	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001596	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001903	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001970	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002097	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002107	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002110	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002150	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002206	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002240	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002716	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002733	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002781	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002921	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002922	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0003072	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0003701	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0004756	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0007734	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0009830	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0010310	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0010628	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0011024	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0011675	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0011801	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0011850	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0012062	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0012243	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0012722	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0030146	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0030872	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0033505	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0040186	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0100699	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0200035	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000821	ORPHA:797	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000834	ORPHA:797	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000554	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001386	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001410	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001824	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001873	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001882	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0001945	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002088	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002094	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002103	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0002202	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0003011	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0011121	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0012219	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0012378	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0012735	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0100749	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0100828	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0200036	ORPHA:797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000083	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000121	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000433	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000501	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:797	Sarcoidosis		HP:0000502	ORPHA:797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0000486	ORPHA:799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0001249	ORPHA:799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0001250	ORPHA:799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0001257	ORPHA:799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0001263	ORPHA:799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0001269	ORPHA:799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0002132	ORPHA:799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0002353	ORPHA:799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0002510	ORPHA:799	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:799	Schizencephaly		HP:0007370	ORPHA:799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002487	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002505	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002506	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002579	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0006892	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0007030	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0010864	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0010936	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0012707	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0030391	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002151	ORPHA:391428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002490	ORPHA:391428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0003287	ORPHA:391428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0012379	ORPHA:391428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000618	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000750	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001250	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001252	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001263	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001942	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001943	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002059	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002180	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002376	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0003128	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0011343	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0500170	ORPHA:391428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000252	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000365	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000510	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000546	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000572	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000639	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000648	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000711	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000749	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0000961	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001260	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001264	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001266	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001285	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001332	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001344	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001639	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001640	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001987	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0001999	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002015	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002134	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002311	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391428	HSD10 disease, infantile type		HP:0002421	ORPHA:391428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000028	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000230	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000256	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000286	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000963	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000973	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000974	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001166	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001252	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001263	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001371	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001510	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001642	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001650	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001763	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0004322	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0005328	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0007469	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0009125	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0010511	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0100813	ORPHA:75496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000160	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000431	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000506	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000653	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000938	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000987	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001000	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001075	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001999	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002209	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002652	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003202	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0045075	ORPHA:75496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002751	ORPHA:75496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001382	ORPHA:75496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75496	B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome		HP:0006481	ORPHA:75496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0001382	ORPHA:750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0008873	ORPHA:750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0000926	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0001156	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002515	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002663	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002758	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002761	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002829	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002938	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003016	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003025	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003026	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003312	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0005720	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0006149	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0009803	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0009826	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0010582	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0020152	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0045086	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0100531	ORPHA:750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0001377	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0001387	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002650	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002857	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0002970	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003015	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003090	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003093	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003180	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003756	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0004236	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0004568	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0006460	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0006499	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0008807	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0008833	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0008839	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0009107	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0010579	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0010585	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0100864	ORPHA:750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0003311	ORPHA:750	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:750	Pseudoachondroplasia		HP:0010646	ORPHA:750	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0000023	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0000963	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0000974	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0000978	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0001537	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0002020	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0004322	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0001382	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0030680	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75497	X-linked Ehlers-Danlos syndrome		HP:0100790	ORPHA:75497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000028	ORPHA:752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000037	ORPHA:752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000047	ORPHA:752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000062	ORPHA:752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000789	ORPHA:752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0008665	ORPHA:752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000023	ORPHA:752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0025380	ORPHA:752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0100779	ORPHA:752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000048	ORPHA:752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0000771	ORPHA:752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:752	46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency		HP:0008736	ORPHA:752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0030439	ORPHA:424016	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0002025	ORPHA:424016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0002027	ORPHA:424016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0002584	ORPHA:424016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0002716	ORPHA:424016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0002896	ORPHA:424016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0010622	ORPHA:424016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0012432	ORPHA:424016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0100526	ORPHA:424016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0002035	ORPHA:424016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0100743	ORPHA:424016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424016	Adenocarcinoma of the anal canal		HP:0200042	ORPHA:424016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0030438	ORPHA:424019	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0002027	ORPHA:424019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0002584	ORPHA:424019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0002716	ORPHA:424019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0012740	ORPHA:424019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0002025	ORPHA:424019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0002035	ORPHA:424019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0002896	ORPHA:424019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0010622	ORPHA:424019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0100526	ORPHA:424019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0100743	ORPHA:424019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424019	Squamous cell carcinoma of the anal canal		HP:0200042	ORPHA:424019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0007325	ORPHA:589618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0033049	ORPHA:589618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000252	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000473	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0001249	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0001260	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0002015	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0004322	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0012758	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0031959	ORPHA:589618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000276	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000414	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000639	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000716	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000729	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000739	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000821	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000826	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0001618	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0002425	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0004209	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0007018	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0007256	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0012048	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0031960	ORPHA:589618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28		HP:0000486	ORPHA:589618	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:589618	Dystonia 28	NOT	HP:0011968	ORPHA:589618	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0010763	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0012385	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0012724	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000028	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000365	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000389	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000776	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0001385	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0001513	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0002751	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0002870	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0012393	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0200053	ORPHA:412035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000219	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000272	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000430	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000540	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000677	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000742	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000750	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0000752	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0001047	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0001508	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0001511	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0002013	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0002019	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0002205	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0002342	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0004322	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412035	13q12.3 microdeletion syndrome		HP:0007328	ORPHA:412035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0006517	ORPHA:747	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0000961	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0001217	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0002087	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0002091	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0002094	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0003651	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0010876	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0012418	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0025435	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0030057	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0045051	ORPHA:747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0012735	ORPHA:747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0025391	ORPHA:747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0030830	ORPHA:747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0001824	ORPHA:747	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0001945	ORPHA:747	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0002105	ORPHA:747	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0012378	ORPHA:747	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:747	Autoimmune pulmonary alveolar proteinosis		HP:0100749	ORPHA:747	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001284	ORPHA:746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003201	ORPHA:746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003546	ORPHA:746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001252	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001254	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001324	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001531	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001635	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001638	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001712	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001985	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0002033	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0002901	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003394	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003551	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003756	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0006555	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0007340	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0008872	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0009063	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0009830	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0011808	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0100626	ORPHA:746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0000580	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0000829	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001250	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001259	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001270	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001396	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001653	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0001761	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0002093	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0002359	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0002878	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003324	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003326	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0003487	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0005180	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0008110	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0008138	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0011675	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0030051	ORPHA:746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0002476	ORPHA:746	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0007067	ORPHA:746	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0007141	ORPHA:746	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:746	Mitochondrial trifunctional protein deficiency		HP:0025145	ORPHA:746	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0000488	ORPHA:743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0000963	ORPHA:743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0000979	ORPHA:743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0001000	ORPHA:743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0001933	ORPHA:743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0002204	ORPHA:743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0002625	ORPHA:743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0004418	ORPHA:743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0004420	ORPHA:743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0005293	ORPHA:743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0008065	ORPHA:743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0100659	ORPHA:743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0100758	ORPHA:743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:743	Severe hereditary thrombophilia due to congenital protein S deficiency		HP:0200042	ORPHA:743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000294	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000316	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000347	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000365	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000370	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000457	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000505	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000520	ORPHA:742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000670	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000958	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000962	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000963	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000982	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000989	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0000992	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0001007	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0001166	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0001231	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0001249	ORPHA:742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0001744	ORPHA:742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0001999	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0002205	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0002211	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0002230	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0002240	ORPHA:742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0002715	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0002857	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0003272	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0004349	ORPHA:742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0005280	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0007473	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0007598	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0007703	ORPHA:742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0008065	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0010669	ORPHA:742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0010783	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0012786	ORPHA:742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0200034	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:742	Prolidase deficiency		HP:0200042	ORPHA:742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0000963	ORPHA:745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0000979	ORPHA:745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0001000	ORPHA:745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0001038	ORPHA:745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0002204	ORPHA:745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0004936	ORPHA:745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0005293	ORPHA:745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0008065	ORPHA:745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0100659	ORPHA:745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:745	Severe hereditary thrombophilia due to congenital protein C deficiency		HP:0100758	ORPHA:745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000995	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001000	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001072	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001167	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001482	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001519	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001548	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001555	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002650	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002652	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002808	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0003199	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0003312	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004099	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004326	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004437	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0005306	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0007400	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0007552	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0010816	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0011276	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0012032	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100026	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100555	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100559	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100560	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100764	ORPHA:744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000268	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000311	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000316	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000400	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000896	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001004	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002101	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002204	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004418	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004459	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004490	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0005595	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0006101	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0007565	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0009125	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0010566	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0012721	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0025104	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0032445	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0032446	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0034275	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100730	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100761	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100774	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:6000009	ORPHA:744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000040	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000053	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000105	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000107	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000194	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000256	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000276	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000324	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000369	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000463	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000464	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000486	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000494	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000501	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000508	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000518	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000520	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000545	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000557	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000567	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000670	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000682	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0000873	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001249	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001250	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001363	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001387	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001597	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001645	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001744	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0001822	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002230	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002282	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002664	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002719	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002827	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0002858	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0003019	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0003715	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004209	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0004420	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0005280	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0005916	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0007440	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0007703	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0007818	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0007899	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0008675	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0009594	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0009804	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0009928	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0010497	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0010508	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0010516	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0010788	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0011386	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0030680	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100006	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100521	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100526	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100615	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:0100777	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:744	Proteus syndrome		HP:6000007	ORPHA:744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000546	ORPHA:166035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000707	ORPHA:166035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001156	ORPHA:166035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001999	ORPHA:166035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0004322	ORPHA:166035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000510	ORPHA:166035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000662	ORPHA:166035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000750	ORPHA:166035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001249	ORPHA:166035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001263	ORPHA:166035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0011968	ORPHA:166035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000023	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000028	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000085	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000107	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000347	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000369	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000400	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000430	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000494	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000512	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000561	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000818	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0000957	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001123	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001319	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001363	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001511	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001596	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001629	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001763	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001792	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0001822	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0002007	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0002120	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0002194	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0002223	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0002342	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0005345	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0005871	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0007099	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0008064	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0010049	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0010761	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0030148	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166035	Brachydactyly-short stature-retinitis pigmentosa syndrome		HP:0030455	ORPHA:166035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002540	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0007164	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0001249	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0001250	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0001265	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0001621	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0001761	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002066	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002304	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002650	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0004305	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0007256	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0007311	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0008969	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0012378	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0012444	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0012638	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0100022	ORPHA:391411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0001336	ORPHA:391411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002362	ORPHA:391411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002425	ORPHA:391411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0000338	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0001332	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002063	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002067	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002172	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391411	Atypical juvenile parkinsonism		HP:0002322	ORPHA:391411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0000017	ORPHA:178029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0000716	ORPHA:178029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0000739	ORPHA:178029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0000873	ORPHA:178029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001250	ORPHA:178029	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001254	ORPHA:178029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001262	ORPHA:178029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001508	ORPHA:178029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001824	ORPHA:178029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001944	ORPHA:178029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001945	ORPHA:178029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0001959	ORPHA:178029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0002014	ORPHA:178029	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0002017	ORPHA:178029	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0002039	ORPHA:178029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0002315	ORPHA:178029	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:178029	Arginine vasopressin deficiency		HP:0002902	ORPHA:178029	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000160	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000233	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000347	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000405	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001525	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001544	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001824	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0007394	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0007485	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0008647	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0011354	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0100678	ORPHA:740	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000050	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000134	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000200	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000218	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000278	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000418	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000436	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000586	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000855	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001376	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001620	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001633	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001646	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001810	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002232	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002362	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002621	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002673	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002827	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002875	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0003292	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0004482	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0005461	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0007418	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0008391	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0008573	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0010296	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0011832	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0012569	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0025168	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0100679	ORPHA:740	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000331	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000444	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000668	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000678	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000684	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000765	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000822	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000894	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000905	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0000961	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001034	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001297	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001387	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001650	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001653	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001658	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001659	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001714	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001718	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001757	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002170	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002223	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002326	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002758	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002781	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0004334	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0004349	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0004380	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0004382	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0006248	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0006335	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0006467	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0007957	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0008800	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0009839	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0009904	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0010505	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0010766	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0010885	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0011079	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0011457	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0012474	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0030002	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0030838	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0030880	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0200034	ORPHA:740	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0001681	ORPHA:740	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0002092	ORPHA:740	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0012804	ORPHA:740	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:740	Hutchinson-Gilford progeria syndrome		HP:0025169	ORPHA:740	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000978	ORPHA:324636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0012531	ORPHA:324636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0031364	ORPHA:324636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0012378	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0025406	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002315	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0001945	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002829	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0003326	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000421	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002239	ORPHA:324636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0005261	ORPHA:324636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000790	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002170	ORPHA:324636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0033676	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0001894	ORPHA:324636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0008352	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0003645	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0001877	ORPHA:324636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0001973	ORPHA:324636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000708	ORPHA:324636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000716	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000739	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000989	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0025474	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000969	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0040064	ORPHA:324636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000271	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002321	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0410019	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002018	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002013	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0002014	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000132	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000712	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0100716	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0030140	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0012233	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0000707	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0008770	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0012076	ORPHA:324636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324636	Autoerythrocyte sensitization syndrome		HP:0031190	ORPHA:324636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002494	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002578	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002591	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002650	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002659	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002870	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0003241	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0005599	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0005616	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0006297	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0006889	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0007018	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0008734	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0010536	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0010829	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0012506	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0012650	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0012743	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0030339	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0034323	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0200055	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0410263	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000217	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000446	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000709	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000729	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000822	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001250	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001262	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001297	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001385	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002013	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002020	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002342	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002500	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002714	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0005978	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0007874	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0008245	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0011470	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0011748	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0011787	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0012166	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0012411	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0012412	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0031100	ORPHA:739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000826	ORPHA:739	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0011734	ORPHA:739	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000028	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000739	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000789	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001252	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001270	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001510	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002015	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0004322	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0008872	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0025160	ORPHA:739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000046	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000059	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000060	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000064	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000135	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000164	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000486	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000540	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000545	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000678	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000704	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000708	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000750	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000786	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000823	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000824	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000938	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000939	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0000969	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001010	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001055	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001256	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001265	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001328	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001508	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001558	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001612	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001773	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0001999	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002033	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002119	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:739	Prader-Willi syndrome		HP:0002205	ORPHA:739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:735	Porokeratosis of Mibelli		HP:0000962	ORPHA:735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:735	Porokeratosis of Mibelli		HP:0000989	ORPHA:735	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:735	Porokeratosis of Mibelli		HP:0000992	ORPHA:735	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:735	Porokeratosis of Mibelli		HP:0008065	ORPHA:735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:735	Porokeratosis of Mibelli		HP:0200044	ORPHA:735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000252	ORPHA:391408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000819	ORPHA:391408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001249	ORPHA:391408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001518	ORPHA:391408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0003508	ORPHA:391408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0011451	ORPHA:391408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000823	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001250	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001263	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001511	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001943	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001999	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002465	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0004325	ORPHA:391408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000160	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000219	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000274	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000275	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000286	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000293	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000294	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000311	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000322	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000341	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000343	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000347	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000400	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000407	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000445	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000463	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000470	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000494	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000592	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000601	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000664	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000677	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000685	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000767	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0000821	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001238	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001321	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001348	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001382	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001620	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0001946	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002079	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002136	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002213	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002313	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002365	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002460	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002650	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002714	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0002751	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0003196	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0007258	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0008070	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0008081	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0008850	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0008936	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0010344	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0010864	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0011308	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0012448	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0025383	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0030084	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome		HP:0200021	ORPHA:391408	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0000972	ORPHA:737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0025528	ORPHA:737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0040211	ORPHA:737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0045059	ORPHA:737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0100872	ORPHA:737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0200035	ORPHA:737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0200044	ORPHA:737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0000989	ORPHA:737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0002814	ORPHA:737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:737	Porokeratosis plantaris palmaris et disseminata		HP:0011354	ORPHA:737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001252	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002829	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002960	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0003236	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0003457	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0003701	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0004303	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0012544	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0012735	ORPHA:732	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001369	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001824	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001945	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002019	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002039	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002093	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002875	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0003326	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0003493	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0006530	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0012378	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0033713	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034143	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034145	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034146	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034147	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034148	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034149	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034150	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034151	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0034152	ORPHA:732	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0000091	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0000934	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0000988	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001288	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001315	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001608	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001611	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001618	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001633	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001635	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001639	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001644	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001658	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001701	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0001894	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002020	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002027	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002068	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002206	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002239	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002240	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0002633	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0003565	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0004936	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0005150	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0011675	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0030880	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0031352	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0100595	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:732	Polymyositis		HP:0100827	ORPHA:732	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000105	ORPHA:731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000113	ORPHA:731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000822	ORPHA:731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001395	ORPHA:731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001405	ORPHA:731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000083	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001396	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001409	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001510	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001562	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001744	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001971	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002040	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002089	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002612	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002630	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002878	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002902	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0003774	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0004905	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0005565	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0006560	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0011040	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0011892	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0011968	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0012202	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0030948	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0100512	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0100513	ORPHA:731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000010	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000952	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001433	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001541	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001873	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001919	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001959	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002239	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002243	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002791	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002884	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0006532	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0030151	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0100520	ORPHA:731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000347	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000369	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0000457	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0001737	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0002108	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0030153	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0040064	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:731	Autosomal recessive polycystic kidney disease		HP:0100543	ORPHA:731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0030434	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0030692	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0031459	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0040274	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0100575	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0100646	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0200040	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0003003	ORPHA:733	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0005227	ORPHA:733	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0007378	ORPHA:733	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0007649	ORPHA:733	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0100245	ORPHA:733	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0200063	ORPHA:733	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0000164	ORPHA:733	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0002014	ORPHA:733	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0002019	ORPHA:733	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0004394	ORPHA:733	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0004783	ORPHA:733	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0025388	ORPHA:733	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0100246	ORPHA:733	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0000706	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0000820	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0002895	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0006771	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0008256	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0010615	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0011068	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0011069	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0100631	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0100717	ORPHA:733	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0000821	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0000853	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0001733	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0002884	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0002885	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0002888	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0002893	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0005230	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0006725	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0009592	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0010614	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0011355	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0012032	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0012126	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:733	Familial adenomatous polyposis		HP:0030153	ORPHA:733	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000505	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000510	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000662	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001133	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001263	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001508	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0002240	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0003323	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0004322	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0008167	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0010571	ORPHA:772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000365	ORPHA:772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000407	ORPHA:772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000639	ORPHA:772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000708	ORPHA:772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001251	ORPHA:772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001252	ORPHA:772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001257	ORPHA:772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000271	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000518	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0000648	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001250	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0001638	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0005930	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0008064	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0010628	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:772	Infantile Refsum disease		HP:0011675	ORPHA:772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0000214	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0000227	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0000421	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0000434	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001009	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0004406	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0100579	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0100585	ORPHA:774	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001409	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001903	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002076	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0006548	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0006574	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0011025	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0100026	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0100761	ORPHA:774	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0000524	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001250	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001342	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001394	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001399	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0001635	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002040	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002092	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002105	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002138	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002204	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002239	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002326	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002408	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0002629	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0004936	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0007763	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0100659	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0100784	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:774	Hereditary hemorrhagic telangiectasia		HP:0200008	ORPHA:774	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000083	ORPHA:773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000458	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000478	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000488	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000496	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000504	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000505	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000508	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000518	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000529	ORPHA:773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000568	ORPHA:773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000639	ORPHA:773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000662	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000958	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001251	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001638	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001744	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000407	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0000616	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001252	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001760	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001761	ORPHA:773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001765	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0001939	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0002093	ORPHA:773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0002164	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0002376	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0002652	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0003202	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0004374	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0005930	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0007256	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0007703	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0008064	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0009830	ORPHA:773	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0010049	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0010864	ORPHA:773	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:773	Refsum disease		HP:0012722	ORPHA:773	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0000716	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0000738	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0000739	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0001250	ORPHA:770	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0001645	ORPHA:770	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0001945	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0002014	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0002017	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0002039	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0002076	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0003401	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0003781	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0004372	ORPHA:770	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0007018	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0100021	ORPHA:770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0100776	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0100785	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0000708	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:770	Rabies		HP:0001604	ORPHA:770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0001945	ORPHA:324625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0002829	ORPHA:324625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0012378	ORPHA:324625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000745	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000988	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0001369	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0001386	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0001387	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0002315	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0003326	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0005198	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0007483	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0010741	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0010783	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0012733	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0030834	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0030839	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0040186	ORPHA:324625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000225	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000282	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000421	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000613	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000716	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000967	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000989	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0000992	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0001892	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0002013	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0002014	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0007473	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0008066	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0009830	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0012219	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0025143	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0025232	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0025289	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0025337	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0032063	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0040165	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0100686	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0100769	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0200037	ORPHA:324625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0001250	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0002383	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0002716	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0002797	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0003401	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0003406	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0012185	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0030880	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324625	Chikungunya		HP:0031002	ORPHA:324625	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001260	ORPHA:412057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001272	ORPHA:412057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002070	ORPHA:412057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002078	ORPHA:412057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001166	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001181	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001288	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001347	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002172	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002317	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001288	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0005328	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0010831	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0012896	ORPHA:412057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000135	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000365	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000602	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000639	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000640	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000666	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001263	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001321	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002015	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002061	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002063	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002167	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002174	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002346	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002354	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002378	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0003693	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0006801	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0007371	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0011098	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0011448	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0012104	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0012110	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0100543	ORPHA:412057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000501	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000657	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000789	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000821	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0000876	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001094	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001105	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001152	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001250	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001596	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001733	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0001999	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0002679	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0005978	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0012547	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0012569	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency		HP:0100651	ORPHA:412057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66518	Short fifth metacarpals-insulin resistance syndrome		HP:0000842	ORPHA:66518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66518	Short fifth metacarpals-insulin resistance syndrome		HP:0004322	ORPHA:66518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66518	Short fifth metacarpals-insulin resistance syndrome		HP:0001744	ORPHA:66518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66518	Short fifth metacarpals-insulin resistance syndrome		HP:0004444	ORPHA:66518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66518	Short fifth metacarpals-insulin resistance syndrome		HP:0010047	ORPHA:66518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66518	Short fifth metacarpals-insulin resistance syndrome		HP:0001742	ORPHA:66518	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0003758	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0004322	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0008283	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0008665	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0008850	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0011998	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0012542	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000998	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001007	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001249	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001263	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001511	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0002719	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0003162	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000040	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000164	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000678	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000831	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000855	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000956	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000958	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0030088	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0030348	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0030796	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0031452	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0100874	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0100879	ORPHA:769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000121	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000158	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000212	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000218	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000221	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000280	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000294	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000303	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000400	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000426	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000445	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000463	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000488	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000821	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0000826	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001629	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001631	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001638	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001953	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0001959	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0002216	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0002750	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0002900	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0006288	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0007305	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0009830	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0010442	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0012686	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:769	Rabson-Mendenhall syndrome		HP:0040270	ORPHA:769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000218	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000243	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000252	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000275	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000286	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000316	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000343	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000431	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000496	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000582	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0000767	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001012	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001250	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001251	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001252	ORPHA:765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001254	ORPHA:765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001257	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001260	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001263	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001266	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001288	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001332	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001337	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001510	ORPHA:765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001511	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0001999	ORPHA:765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0002007	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0002094	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0002119	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0002789	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0007256	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0007370	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0008872	ORPHA:765	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0100021	ORPHA:765	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:765	Pyruvate dehydrogenase deficiency		HP:0100453	ORPHA:765	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0000316	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0000347	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0000455	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0000582	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0000766	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0001156	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0002650	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0002656	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0002663	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0002857	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0003038	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0003071	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0003083	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0004322	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0008905	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0010585	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0100168	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0410005	ORPHA:166016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0006380	ORPHA:166016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166016	Multiple epiphyseal dysplasia, Lowry type		HP:0006471	ORPHA:166016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0000083	ORPHA:764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0001482	ORPHA:764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0001645	ORPHA:764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0001824	ORPHA:764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0001945	ORPHA:764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0001974	ORPHA:764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0002719	ORPHA:764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0003326	ORPHA:764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0100614	ORPHA:764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0100616	ORPHA:764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0100806	ORPHA:764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:764	Pyomyositis		HP:0100838	ORPHA:764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0011121	ORPHA:767	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0000077	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0001824	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0001945	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0002829	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0003326	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0005764	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0009830	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0011227	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0031003	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0033260	ORPHA:767	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0000707	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0000822	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0000965	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0001482	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0001701	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0002011	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0002027	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0002088	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0003390	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0010783	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0011024	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0030680	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0030880	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0200042	ORPHA:767	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0000478	ORPHA:767	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0001638	ORPHA:767	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:767	Polyarteritis nodosa		HP:0002102	ORPHA:767	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0001744	ORPHA:766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0001903	ORPHA:766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0001923	ORPHA:766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0004870	ORPHA:766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0008282	ORPHA:766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0025109	ORPHA:766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0001789	ORPHA:766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0003281	ORPHA:766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0003452	ORPHA:766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0004804	ORPHA:766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0006579	ORPHA:766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0001877	ORPHA:766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0004447	ORPHA:766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0011273	ORPHA:766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:766	Hemolytic anemia due to red cell pyruvate kinase deficiency		HP:0012463	ORPHA:766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0003236	ORPHA:206559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0006785	ORPHA:206559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0030099	ORPHA:206559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0001328	ORPHA:206559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0002194	ORPHA:206559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0001288	ORPHA:206559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0003551	ORPHA:206559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0007126	ORPHA:206559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0030197	ORPHA:206559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0100543	ORPHA:206559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0001263	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0001644	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0002119	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0002540	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0003691	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0003697	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0006913	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0008981	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0011712	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206559	POMT2-related limb-girdle muscular dystrophy R14		HP:0025169	ORPHA:206559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000790	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000978	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000979	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000988	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002017	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002027	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002633	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002829	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0005244	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0200039	ORPHA:761	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0001369	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0001945	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002039	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002076	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002383	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0003326	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0010783	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0011276	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0100796	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0200042	ORPHA:761	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000083	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000093	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000648	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0000969	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0001025	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0001250	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0001324	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002091	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0002239	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0004374	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0012733	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0100534	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0100665	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:761	Immunoglobulin A vasculitis		HP:0100820	ORPHA:761	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0002843	ORPHA:760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0011935	ORPHA:760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0000707	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001890	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0002205	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0002719	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0002960	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0003537	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0004430	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0005363	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0032166	ORPHA:760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0000708	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0000752	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001249	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001251	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001252	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001257	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001263	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001276	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001888	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0002313	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0002664	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0011442	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0045080	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0100021	ORPHA:760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0000407	ORPHA:760	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001297	ORPHA:760	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0001973	ORPHA:760	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:760	Purine nucleoside phosphorylase deficiency		HP:0002725	ORPHA:760	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001156	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002007	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0004474	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0005446	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0005906	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0008873	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0009839	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0011001	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0030353	ORPHA:763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000164	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000270	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000327	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000347	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000444	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000448	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000520	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000592	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000824	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001511	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001597	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001773	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002659	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002870	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0005789	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0008598	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0009381	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0011800	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0012532	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0200055	ORPHA:763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000218	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000668	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000670	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000680	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000689	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000696	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000889	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001601	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001807	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002164	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002645	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002650	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002866	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0003027	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0003302	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0003304	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0006297	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0006335	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0008905	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0010307	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0010884	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0011342	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0025502	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0100559	ORPHA:763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000486	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000539	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000707	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0000774	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001382	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0001433	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002308	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002493	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002516	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0002808	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0003307	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0004440	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:763	Pycnodysostosis		HP:0007266	ORPHA:763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000750	ORPHA:436003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001270	ORPHA:436003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000162	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000175	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000347	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000396	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001166	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001167	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001385	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001762	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0002870	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0002974	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0003396	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0009778	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0012430	ORPHA:436003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000023	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000047	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000394	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000430	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000486	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000494	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0000612	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001239	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001631	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001840	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0001845	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0002360	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0002687	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0002705	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0002944	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0004969	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0007099	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0007359	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0008551	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0009929	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436003	Contractures-developmental delay-Pierre Robin syndrome		HP:0025100	ORPHA:436003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0012663	ORPHA:66529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0010872	ORPHA:66529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0012251	ORPHA:66529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0031483	ORPHA:66529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0100749	ORPHA:66529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0410174	ORPHA:66529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0000822	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001513	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001657	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001681	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001962	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0002013	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0002094	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0002615	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0005184	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0006698	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0008180	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0009805	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0012250	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0025077	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0031138	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:6001073	ORPHA:66529	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001250	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001279	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001653	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001662	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001663	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0001727	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0004308	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0005110	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0011675	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0030149	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy		HP:0100598	ORPHA:66529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy	NOT	HP:0001677	ORPHA:66529	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy	NOT	HP:0005145	ORPHA:66529	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy	NOT	HP:0006704	ORPHA:66529	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:66529	Tako-Tsubo cardiomyopathy	NOT	HP:0012819	ORPHA:66529	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000474	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000488	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000573	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000951	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001102	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0007392	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0030680	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0100545	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0100659	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0100679	ORPHA:758	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000978	ORPHA:758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001065	ORPHA:758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001582	ORPHA:758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0004417	ORPHA:758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0025473	ORPHA:758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0033027	ORPHA:758	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000121	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000505	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000592	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000765	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000822	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0000974	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001012	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001297	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001482	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001634	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001645	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001650	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001681	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001723	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001872	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0002172	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0002239	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0002326	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0002514	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0004306	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0001382	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0011506	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0012508	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0100585	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:758	Pseudoxanthoma elasticum		HP:0100817	ORPHA:758	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0000164	ORPHA:757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0000682	ORPHA:757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0000822	ORPHA:757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0001324	ORPHA:757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0001510	ORPHA:757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0002017	ORPHA:757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0002153	ORPHA:757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0003768	ORPHA:757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:757	Pseudohypoaldosteronism type 2		HP:0004322	ORPHA:757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0002938	ORPHA:206546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0003236	ORPHA:206546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0003701	ORPHA:206546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0001435	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0001644	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0001712	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0002540	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0002942	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0002943	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0003324	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0003326	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0003394	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0003710	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0003731	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0008981	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0030097	ORPHA:206546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0001635	ORPHA:206546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers		HP:0002987	ORPHA:206546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	NOT	HP:0002380	ORPHA:206546	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:206546	Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers	NOT	HP:0003409	ORPHA:206546	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0000008	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0000098	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0000151	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0000786	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0003251	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0008655	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0008689	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0008730	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0011969	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0012888	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0025134	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0030088	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0040314	ORPHA:99429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0000823	ORPHA:99429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0002215	ORPHA:99429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0002221	ORPHA:99429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0002225	ORPHA:99429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0002555	ORPHA:99429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0031102	ORPHA:99429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0010788	ORPHA:99429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0001061	ORPHA:99429	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0030346	ORPHA:99429	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99429	Complete androgen insensitivity syndrome		HP:0100728	ORPHA:99429	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000028	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000033	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000046	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000048	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000051	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000062	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000144	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0000818	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0008736	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:753	46,XY difference of sex development due to 5-alpha-reductase 2 deficiency		HP:0100779	ORPHA:753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:55881	Adamantinoma		HP:0002653	ORPHA:55881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:55881	Adamantinoma		HP:0002756	ORPHA:55881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:55881	Adamantinoma		HP:0003072	ORPHA:55881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0001638	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0002913	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0002987	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003089	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003691	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0006466	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0008981	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0009129	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0010628	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0012785	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003326	ORPHA:206549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0006785	ORPHA:206549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0008994	ORPHA:206549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0009053	ORPHA:206549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0001430	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0002816	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003236	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003445	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003458	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003482	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003555	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003557	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003730	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0003738	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0004303	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0007210	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0008988	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0008997	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0009050	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0012548	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0031237	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0100295	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0100297	ORPHA:206549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0001239	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206549	Anoctamin-5-related limb-girdle muscular dystrophy R12		HP:0001371	ORPHA:206549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000026	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000028	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000037	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000047	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000054	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000062	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000118	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000134	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000151	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000786	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000811	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000812	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000815	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000837	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0002750	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0008187	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0008193	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0010790	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0040171	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0100783	ORPHA:755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000030	ORPHA:755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0000869	ORPHA:755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:755	Leydig cell hypoplasia		HP:0012872	ORPHA:755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0000207	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0000256	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0000316	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0000431	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0000767	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0000924	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0001249	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002007	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002419	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002654	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002663	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002857	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0003037	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0030084	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0031092	ORPHA:166024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0001274	ORPHA:166024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002079	ORPHA:166024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002829	ORPHA:166024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0004322	ORPHA:166024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0002059	ORPHA:166024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0012725	ORPHA:166024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:166024	Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome		HP:0003468	ORPHA:166024	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0000473	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0001336	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0001618	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0002317	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0002346	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0001288	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0002356	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0002530	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0004373	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0012179	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0012893	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0200085	ORPHA:420492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0002883	ORPHA:420492	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0005115	ORPHA:420492	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0025269	ORPHA:420492	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0001272	ORPHA:420492	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:420492	Adult-onset cervical dystonia, DYT23 type		HP:0002120	ORPHA:420492	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000431	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000494	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000506	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000508	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000581	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000609	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000648	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000750	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001263	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002342	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000126	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000248	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000278	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000340	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000341	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000369	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000411	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000160	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000218	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000232	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000252	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000286	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000319	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000343	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000426	ORPHA:261349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000486	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000505	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000527	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000717	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000729	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001182	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001252	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001290	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001508	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001510	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001511	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001840	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002061	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002205	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0005274	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0006610	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0007018	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0100490	ORPHA:261349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000003	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000023	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000098	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000135	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000348	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000365	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000767	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0000771	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001260	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001288	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001321	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001561	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001601	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001611	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001653	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001659	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001763	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001852	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0001863	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002015	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002119	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002213	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002353	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002558	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002650	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002808	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0002999	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0005487	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0007598	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0008734	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0010628	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0011968	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0045075	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261349	2p15p16.1 microdeletion syndrome		HP:0100625	ORPHA:261349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93283	Spondyloepiphyseal dysplasia, Kimberley type		HP:0000926	ORPHA:93283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93283	Spondyloepiphyseal dysplasia, Kimberley type		HP:0002655	ORPHA:93283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93283	Spondyloepiphyseal dysplasia, Kimberley type		HP:0002758	ORPHA:93283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93283	Spondyloepiphyseal dysplasia, Kimberley type		HP:0002983	ORPHA:93283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93283	Spondyloepiphyseal dysplasia, Kimberley type		HP:0003508	ORPHA:93283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93283	Spondyloepiphyseal dysplasia, Kimberley type		HP:0005930	ORPHA:93283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93283	Spondyloepiphyseal dysplasia, Kimberley type		HP:0010306	ORPHA:93283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000003	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000028	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000046	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000062	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000126	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000160	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000175	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000238	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000256	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000308	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000316	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000356	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000369	ORPHA:261344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000445	ORPHA:261344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000476	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000494	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000528	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000601	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000772	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0000776	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001166	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001177	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001274	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001321	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001539	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001561	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001629	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001643	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001770	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001789	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001800	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0001833	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0002007	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0002023	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0002119	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0005280	ORPHA:261344	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0006610	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0008386	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0008676	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0010306	ORPHA:261344	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0010880	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261344	Trisomy 1q syndrome		HP:0100490	ORPHA:261344	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0000926	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0001508	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0001552	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002654	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003051	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003088	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003521	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0004594	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0005775	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0012771	ORPHA:93284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0000470	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0001376	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0001386	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002763	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002829	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002945	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003043	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003365	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003418	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003855	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0005086	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0008843	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0010656	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0011001	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0030839	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0100569	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0100712	ORPHA:93284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002650	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002751	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002812	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002938	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002942	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0002996	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003311	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003832	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0004586	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0004637	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0006233	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0006248	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0006467	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0008812	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0009763	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0010231	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0010575	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0025131	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0025263	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0040161	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0100864	ORPHA:93284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda		HP:0003401	ORPHA:93284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda	NOT	HP:0000175	ORPHA:93284	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda	NOT	HP:0000541	ORPHA:93284	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda	NOT	HP:0002960	ORPHA:93284	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda	NOT	HP:0012649	ORPHA:93284	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93284	Spondyloepiphyseal dysplasia tarda	NOT	HP:0100769	ORPHA:93284	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000085	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000212	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000218	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000252	ORPHA:46059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000286	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000293	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000340	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000341	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000343	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000347	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000365	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000414	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000463	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000482	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000494	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000508	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0000518	ORPHA:46059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001162	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001250	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001252	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001263	ORPHA:46059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001328	ORPHA:46059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001336	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001399	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001406	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001508	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001511	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001770	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001830	ORPHA:46059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001873	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0001883	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0002240	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0002308	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0002435	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0002514	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0002714	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0003196	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0004422	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0004823	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0005487	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0007759	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0008278	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0008736	ORPHA:46059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0011875	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:46059	Lathosterolosis		HP:0100711	ORPHA:46059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0001250	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0001257	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0001302	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0001319	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0002119	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0002187	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0002282	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0002521	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0008936	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0010864	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0011201	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0011968	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0012469	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0012758	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0020219	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0031882	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1084	Isolated lissencephaly type 1 without known genetic defects		HP:0100952	ORPHA:1084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0000252	ORPHA:1083	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0000750	ORPHA:1083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0001263	ORPHA:1083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0002079	ORPHA:1083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0007190	ORPHA:1083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0007266	ORPHA:1083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0010864	ORPHA:1083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0025190	ORPHA:1083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0001276	ORPHA:1083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0001339	ORPHA:1083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0001347	ORPHA:1083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0001999	ORPHA:1083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0002119	ORPHA:1083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0002120	ORPHA:1083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0006891	ORPHA:1083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0001272	ORPHA:1083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0001302	ORPHA:1083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0002090	ORPHA:1083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0002126	ORPHA:1083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0007165	ORPHA:1083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0009879	ORPHA:1083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1083	Microlissencephaly		HP:0032391	ORPHA:1083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0000791	ORPHA:411543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0001997	ORPHA:411543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0002149	ORPHA:411543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0003149	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0003240	ORPHA:411543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0012759	ORPHA:411543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0000083	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0000407	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0000707	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0001249	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0001252	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0001369	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0020074	ORPHA:411543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0001251	ORPHA:411543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0001919	ORPHA:411543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0007178	ORPHA:411543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0009830	ORPHA:411543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0000501	ORPHA:411543	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0000545	ORPHA:411543	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0001263	ORPHA:411543	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411543	Severe phosphoribosylpyrophosphate synthetase superactivity		HP:0002205	ORPHA:411543	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000308	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000327	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000343	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000505	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000506	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000518	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000541	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000545	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002652	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002829	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000272	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000286	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0003196	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0003312	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0004327	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0005280	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0005930	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0011800	ORPHA:828	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000158	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000162	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000175	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000193	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000204	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000347	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000365	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000389	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000407	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000457	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000463	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000483	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000520	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000768	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000926	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001166	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001252	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001373	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001519	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001634	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002020	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002205	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002650	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002653	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002758	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002808	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002857	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0003302	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001382	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0006461	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0007992	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0011003	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0011530	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0011675	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0031153	ORPHA:828	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000316	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000486	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000501	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000519	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000554	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000618	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000682	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0000940	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001083	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0001533	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0002827	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0003179	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0003202	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0003416	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0004322	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0004326	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0004349	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0004374	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0006288	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0008872	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0009804	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0010290	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0010807	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:828	Stickler syndrome		HP:0031154	ORPHA:828	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0000531	ORPHA:98969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0001939	ORPHA:98969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0007759	ORPHA:98969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0007856	ORPHA:98969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0000495	ORPHA:98969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0001141	ORPHA:98969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0100689	ORPHA:98969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0000484	ORPHA:98969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0000613	ORPHA:98969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0012155	ORPHA:98969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98969	Macular corneal dystrophy		HP:0200026	ORPHA:98969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0030057	ORPHA:398124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0000951	ORPHA:398124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001392	ORPHA:398124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001871	ORPHA:398124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0000238	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0000962	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0000988	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0000992	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001036	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001644	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001678	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001873	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001875	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001903	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0002240	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0002500	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0002910	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0011675	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0012722	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0025300	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0025474	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0040186	ORPHA:398124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0000256	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001399	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001627	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001657	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001744	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001876	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001878	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001892	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0001915	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0002086	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0002135	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0002652	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus		HP:0011702	ORPHA:398124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398124	Neonatal lupus erythematosus	NOT	HP:0001396	ORPHA:398124	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0007663	ORPHA:827	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0000493	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0000551	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0000603	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0000608	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0000610	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0000649	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0000662	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0007704	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0007722	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0007814	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0008002	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0030329	ORPHA:827	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0008059	ORPHA:827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0030500	ORPHA:827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:827	Stargardt disease		HP:0030786	ORPHA:827	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0000988	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0000989	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001369	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001386	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001945	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001974	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002829	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0003281	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0003565	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0005059	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0010783	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0011227	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0011897	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0012378	ORPHA:829	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001744	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001824	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001903	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002027	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002102	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002202	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002240	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002716	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002910	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0003155	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0003326	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0005828	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0008940	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0025406	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0025439	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0033050	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0040186	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:6000933	ORPHA:829	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0000093	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001298	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001701	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0001733	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002018	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002039	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002098	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002840	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0002923	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0003119	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0003493	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0005528	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0006515	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0012115	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0012156	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0012544	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0012819	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0100773	ORPHA:829	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0000509	ORPHA:829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0000554	ORPHA:829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0005521	ORPHA:829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0011034	ORPHA:829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0033430	ORPHA:829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease		HP:0100534	ORPHA:829	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease	NOT	HP:0002665	ORPHA:829	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease	NOT	HP:0031693	ORPHA:829	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:829	Adult-onset Still disease	NOT	HP:0100806	ORPHA:829	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0005561	ORPHA:824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0000980	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001433	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001744	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001871	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001873	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001903	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0002240	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0012143	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0012378	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0025142	ORPHA:824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0000967	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0000979	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001409	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001876	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001892	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001894	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001945	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001974	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001977	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001978	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0002039	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0002716	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0003388	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0004420	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0004447	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0004936	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0011134	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0030157	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0031020	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0031364	ORPHA:824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0001028	ORPHA:824	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0004326	ORPHA:824	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0004377	ORPHA:824	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis		HP:0025435	ORPHA:824	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:824	Primary myelofibrosis	NOT	HP:0030057	ORPHA:824	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000077	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000238	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000256	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000365	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000520	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000774	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000926	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000944	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0000956	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001156	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001250	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001252	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001360	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001376	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001561	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001582	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001631	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001643	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002007	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002084	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002093	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002119	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002269	ORPHA:93274	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002652	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002676	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002808	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0002983	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0004322	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0005280	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0001382	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0006703	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0010306	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0010880	ORPHA:93274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0012368	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93274	Thanatophoric dysplasia type 2		HP:0100543	ORPHA:93274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0000708	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0000965	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001727	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002076	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002120	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002315	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002321	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002354	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0007141	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0011276	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0100545	ORPHA:820	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0000726	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0000822	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001123	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001268	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001269	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001270	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001324	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001653	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001659	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002326	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002376	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0007359	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0010794	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0011714	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0012213	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0025722	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0031987	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0100543	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0100576	ORPHA:820	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0000093	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0000112	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0000716	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001250	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001337	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0001647	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002072	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002170	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002381	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0003613	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0009710	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0009830	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0012246	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0020166	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0025342	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0030773	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0030880	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0033126	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0100704	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:5200330	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:6000139	ORPHA:820	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0002138	ORPHA:820	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0030746	ORPHA:820	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:820	Sneddon syndrome		HP:0033260	ORPHA:820	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0001269	ORPHA:444463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0001744	ORPHA:444463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0001878	ORPHA:444463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0002960	ORPHA:444463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0001890	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0001973	ORPHA:444463	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0000403	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0001297	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0001888	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0002716	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0002725	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0011343	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0011947	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444463	Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency		HP:0012115	ORPHA:444463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0000531	ORPHA:98962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0007881	ORPHA:98962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0000495	ORPHA:98962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0000505	ORPHA:98962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0011493	ORPHA:98962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0000613	ORPHA:98962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0007663	ORPHA:98962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0008039	ORPHA:98962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0011495	ORPHA:98962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98962	Granular corneal dystrophy type I		HP:0200026	ORPHA:98962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0005502	ORPHA:822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0000952	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0000980	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001081	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001324	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001744	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001903	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001923	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0002240	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0002904	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0004444	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0005525	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0011900	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0025548	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0100724	ORPHA:822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001251	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001723	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001945	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001978	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0002027	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0003326	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0025143	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0040186	ORPHA:822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001510	ORPHA:822	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0001997	ORPHA:822	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0003270	ORPHA:822	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:822	Hereditary spherocytosis		HP:0200042	ORPHA:822	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0000531	ORPHA:98963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0007802	ORPHA:98963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0011493	ORPHA:98963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0000505	ORPHA:98963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0007663	ORPHA:98963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0007759	ORPHA:98963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0008039	ORPHA:98963	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0000495	ORPHA:98963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98963	Granular corneal dystrophy type II		HP:0000622	ORPHA:98963	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0000481	ORPHA:98964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0000559	ORPHA:98964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0000572	ORPHA:98964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0001149	ORPHA:98964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0007957	ORPHA:98964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0011493	ORPHA:98964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0000483	ORPHA:98964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0000495	ORPHA:98964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0000613	ORPHA:98964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0008039	ORPHA:98964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0012040	ORPHA:98964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0025337	ORPHA:98964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0200026	ORPHA:98964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0007924	ORPHA:98964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0008511	ORPHA:98964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0011003	ORPHA:98964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98964	Lattice corneal dystrophy type I		HP:0012155	ORPHA:98964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000098	ORPHA:821	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000280	ORPHA:821	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0012771	ORPHA:821	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000268	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000275	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000276	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000365	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000389	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000483	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000494	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000708	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001250	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001252	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001256	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001263	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001382	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002019	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002650	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0004768	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0005616	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0006579	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0011220	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0011968	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0031284	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0040194	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0400000	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0410263	ORPHA:821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000076	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000077	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000083	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000164	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000256	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000718	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000729	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000739	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001176	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001320	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001337	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001371	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001627	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001629	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001631	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001643	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001763	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002020	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002059	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002069	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002119	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002121	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002123	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002280	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002342	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002311	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002384	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002389	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002442	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002808	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0004942	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0007370	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0010741	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0010864	ORPHA:821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000023	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000028	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000034	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000047	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000073	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000074	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000104	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000126	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000144	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000405	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000486	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000518	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000540	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000545	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000639	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000668	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000696	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000767	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000821	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0000953	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001010	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001028	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001363	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001537	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001741	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001762	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001792	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0001998	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002251	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0002664	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0003006	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0003072	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0003273	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0003468	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0004691	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0005617	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0006466	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0006721	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0007018	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0006349	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0009592	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0009797	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0010957	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0030357	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0030736	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:821	Sotos syndrome		HP:0032447	ORPHA:821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000028	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000122	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000158	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000218	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000238	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000252	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000256	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000280	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000286	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000303	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000316	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000319	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000322	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000325	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000337	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000343	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000347	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000369	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000411	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000414	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000445	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000457	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000465	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000486	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000490	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000494	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000582	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000588	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0000960	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001182	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001249	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001250	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001252	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001260	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001263	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001618	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001629	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001643	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001704	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001770	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001800	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0001836	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0002007	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0002023	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0002162	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0002463	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0002650	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0004422	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0005180	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0007018	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0009738	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0009795	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0011039	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0012471	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0100022	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0100490	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261337	Distal 22q11.2 microduplication syndrome		HP:0100540	ORPHA:261337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0007881	ORPHA:98960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0007924	ORPHA:98960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0008039	ORPHA:98960	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0000495	ORPHA:98960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0000613	ORPHA:98960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0007759	ORPHA:98960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0032148	ORPHA:98960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0200026	ORPHA:98960	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98960	Thiel-Behnke corneal dystrophy		HP:0000483	ORPHA:98960	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000773	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000774	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000944	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001773	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002093	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002983	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0003270	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0004279	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0005716	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0008873	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0009106	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0010306	ORPHA:93271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000028	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000062	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000089	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000126	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000204	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000256	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000286	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000343	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000347	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000445	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001162	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001789	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002007	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002612	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0003762	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0004599	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0005280	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0008716	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0008736	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0030680	ORPHA:93271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000107	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0000518	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001177	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001274	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001305	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001321	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0001539	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002006	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002023	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002032	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002089	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0002119	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0004397	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0010297	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		HP:0010564	ORPHA:93271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1074	Ankyloblepharon filiforme adnatum-imperforate anus syndrome		HP:0000028	ORPHA:1074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1074	Ankyloblepharon filiforme adnatum-imperforate anus syndrome		HP:0000175	ORPHA:1074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1074	Ankyloblepharon filiforme adnatum-imperforate anus syndrome		HP:0009755	ORPHA:1074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1074	Ankyloblepharon filiforme adnatum-imperforate anus syndrome		HP:0009804	ORPHA:1074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1074	Ankyloblepharon filiforme adnatum-imperforate anus syndrome		HP:0100335	ORPHA:1074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1072	Ankyloblepharon filiforme adnatum-cleft palate syndrome		HP:0000175	ORPHA:1072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1072	Ankyloblepharon filiforme adnatum-cleft palate syndrome		HP:0009755	ORPHA:1072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1072	Ankyloblepharon filiforme adnatum-cleft palate syndrome		HP:0009775	ORPHA:1072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1072	Ankyloblepharon filiforme adnatum-cleft palate syndrome		HP:0100267	ORPHA:1072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1072	Ankyloblepharon filiforme adnatum-cleft palate syndrome		HP:0100335	ORPHA:1072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000405	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000431	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000966	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0001795	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0001810	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0001812	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0002208	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0008070	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0008391	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0009755	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0100335	ORPHA:1071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000175	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000176	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000347	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000653	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000668	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000682	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000687	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000698	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000982	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0007440	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0011819	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0045075	ORPHA:1071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000411	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0000684	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0001092	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0001608	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0001629	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0002558	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0004209	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1071	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		HP:0006101	ORPHA:1071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000010	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000023	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000160	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000175	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000219	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000252	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000272	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000276	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000307	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000319	ORPHA:261330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000324	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000363	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000407	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000426	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000430	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000453	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000490	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000581	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000657	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000716	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0000722	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001166	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001249	ORPHA:261330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001250	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001263	ORPHA:261330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001510	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001511	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001622	ORPHA:261330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001629	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001631	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001659	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001660	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001763	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001770	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001802	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001817	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001852	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002021	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002205	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002463	ORPHA:261330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002553	ORPHA:261330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002607	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002664	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002673	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002705	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0002721	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0003307	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0004209	ORPHA:261330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0004279	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0004322	ORPHA:261330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0004942	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0001382	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0006487	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0007018	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0009465	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0009795	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0009882	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0010296	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0100033	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261330	Distal 22q11.2 microdeletion syndrome		HP:0100490	ORPHA:261330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1078	Thumb stiffness-brachydactyly-intellectual disability syndrome		HP:0001172	ORPHA:1078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1078	Thumb stiffness-brachydactyly-intellectual disability syndrome		HP:0001249	ORPHA:1078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1078	Thumb stiffness-brachydactyly-intellectual disability syndrome		HP:0001387	ORPHA:1078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1078	Thumb stiffness-brachydactyly-intellectual disability syndrome		HP:0005916	ORPHA:1078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1078	Thumb stiffness-brachydactyly-intellectual disability syndrome		HP:0009370	ORPHA:1078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1078	Thumb stiffness-brachydactyly-intellectual disability syndrome		HP:0001513	ORPHA:1078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000252	ORPHA:816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000488	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000545	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000608	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000613	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000682	ORPHA:816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000958	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0000962	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001025	ORPHA:816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001249	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001250	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001252	ORPHA:816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001257	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001260	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001264	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0001387	ORPHA:816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0002167	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0002650	ORPHA:816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0002652	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0002808	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0004322	ORPHA:816	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0007256	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0007440	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0007703	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0008064	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0010783	ORPHA:816	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0100533	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:816	Sjögren-Larsson syndrome		HP:0200020	ORPHA:816	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1077	Dental ankylosis		HP:0000303	ORPHA:1077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1077	Dental ankylosis		HP:0000682	ORPHA:1077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1077	Dental ankylosis		HP:0004209	ORPHA:1077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1077	Dental ankylosis		HP:0009804	ORPHA:1077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000164	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000248	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000337	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000403	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000431	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000490	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000582	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000664	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000679	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000680	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000733	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000739	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000750	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001156	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001249	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001252	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001263	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001265	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001513	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001609	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002007	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002167	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002360	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0005280	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0005607	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0007018	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0010804	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0011800	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0012689	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0100716	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0100729	ORPHA:819	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000194	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000220	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000280	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000303	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000316	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000321	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000322	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000347	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000405	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000463	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000482	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000486	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000545	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001169	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001288	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001531	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001558	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001627	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001763	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001770	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002019	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002020	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002119	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002155	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002353	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002650	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002788	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0003124	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0003196	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0004209	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0004322	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0006979	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0007328	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0007370	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0008872	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0009830	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0010780	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0025160	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0030051	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0030680	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0032041	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0032508	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0032509	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0100543	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0100710	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:5200360	ORPHA:819	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000069	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000119	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000175	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000204	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000252	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000541	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000821	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000823	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0000826	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001161	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001250	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0001387	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0002720	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0008678	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0010535	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0011675	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0034819	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:819	Smith-Magenis syndrome		HP:0100542	ORPHA:819	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0002149	ORPHA:411536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0003149	ORPHA:411536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0003240	ORPHA:411536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0000791	ORPHA:411536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0001369	ORPHA:411536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0020074	ORPHA:411536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0000083	ORPHA:411536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0001919	ORPHA:411536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0012626	ORPHA:411536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity		HP:0000707	ORPHA:411536	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity	NOT	HP:0000407	ORPHA:411536	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity	NOT	HP:0000478	ORPHA:411536	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity	NOT	HP:0001249	ORPHA:411536	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity	NOT	HP:0001999	ORPHA:411536	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:411536	Mild phosphoribosylpyrophosphate synthetase superactivity	NOT	HP:0009830	ORPHA:411536	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000252	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000347	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000431	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000463	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001249	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001252	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001263	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001510	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002020	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0004322	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0004691	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0006482	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0007477	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0008872	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0010569	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0010880	ORPHA:818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000028	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000047	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000062	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000154	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000175	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000212	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000343	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000358	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000470	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000508	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000717	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000965	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000992	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000996	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001162	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001262	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001511	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001561	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001600	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001629	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001631	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001830	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002089	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002101	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002119	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002360	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002719	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002777	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002827	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0004422	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0005916	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0006610	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0006695	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0007018	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0007360	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0008665	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0008736	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0009623	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0030680	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0100716	ORPHA:818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000003	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000074	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000126	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000171	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000286	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000316	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000407	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000453	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000486	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000494	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000499	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000501	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000518	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000520	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000582	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000612	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000639	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000647	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000648	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000682	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000772	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0000776	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001156	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001171	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001250	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001276	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001360	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001543	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001643	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0001884	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002021	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002251	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002650	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0002808	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0003027	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0003312	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0005264	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0005599	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0006101	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0006288	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0006501	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0007370	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0008056	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0008678	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0008905	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0009465	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0009804	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0010297	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0011069	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:818	Smith-Lemli-Opitz syndrome		HP:0100542	ORPHA:818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000325	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000369	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000592	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001511	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0004322	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0004326	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0004482	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0008897	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0011220	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0011968	ORPHA:813	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000028	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000032	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000233	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000270	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000347	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000358	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000678	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000855	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001270	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001531	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001620	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001622	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001988	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0002019	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0002020	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0002360	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0002714	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0002750	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0002829	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0003199	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0004209	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0008364	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0008734	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0010782	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0011844	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0012412	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0100555	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0100559	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0100560	ORPHA:813	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000047	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000079	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000142	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000729	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000826	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000957	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0000975	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001256	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001513	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001626	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0001852	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0002650	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0005484	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:813	Silver-Russell syndrome		HP:0008935	ORPHA:813	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000179	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000280	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000407	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000431	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000488	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000505	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000518	ORPHA:812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000529	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000639	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000762	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000768	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000943	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0000962	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001249	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001250	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001251	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001252	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001288	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001324	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001336	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001337	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001350	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0001744	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0002007	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0002167	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0002353	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0002650	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0002652	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0002750	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0002808	ORPHA:812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0003202	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0003312	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0003355	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0003461	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0004322	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0007957	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0010306	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0010729	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0011276	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0012061	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0100022	ORPHA:812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:812	Sialidosis type 1		HP:0100790	ORPHA:812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0000613	ORPHA:98957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0000622	ORPHA:98957	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0000643	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0007663	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0008039	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0009926	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0010637	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0011496	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0034804	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0200026	ORPHA:98957	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98957	Gelatinous drop-like corneal dystrophy		HP:0011493	ORPHA:98957	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0000473	ORPHA:420485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0000643	ORPHA:420485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0002451	ORPHA:420485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0007351	ORPHA:420485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0012477	ORPHA:420485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0001336	ORPHA:420485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0001600	ORPHA:420485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0002378	ORPHA:420485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420485	Cranio-cervical dystonia with laryngeal and upper-limb involvement		HP:0012048	ORPHA:420485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000062	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000239	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000316	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000322	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000347	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000369	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000431	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000470	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000518	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000568	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000772	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000774	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000889	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000926	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0000944	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0001274	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0001539	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0001629	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0002007	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0002676	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0002691	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0002714	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0004331	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0005930	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0006487	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0008905	ORPHA:93267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93267	Cloverleaf skull-multiple congenital anomalies syndrome		HP:0009623	ORPHA:93267	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000924	ORPHA:811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001738	ORPHA:811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001871	ORPHA:811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001875	ORPHA:811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001903	ORPHA:811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002630	ORPHA:811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0011024	ORPHA:811	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000708	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001508	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001510	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001873	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001897	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001972	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002570	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002594	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002750	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002863	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0004322	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0004395	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0004905	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0005518	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0011892	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0012202	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0040238	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0100512	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0100513	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0410252	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0410255	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0410289	ORPHA:811	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000246	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000670	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000729	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000736	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000886	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000938	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000988	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001249	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001367	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001627	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001876	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001882	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001909	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001915	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002090	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002718	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002953	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0003016	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0003025	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0004429	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0004808	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0005528	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0005871	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0045027	ORPHA:811	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000155	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000356	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000365	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000684	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000819	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000824	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0000964	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0001167	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002240	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002721	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002754	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0002910	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0006461	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0008064	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0040075	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:811	Shwachman-Diamond syndrome		HP:0100806	ORPHA:811	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001945	ORPHA:810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002027	ORPHA:810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0025086	ORPHA:810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0032155	ORPHA:810	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001944	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001974	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002013	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002018	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002039	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0003111	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0012378	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0012702	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0025406	ORPHA:810	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001531	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001943	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002373	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002590	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002721	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002902	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0025085	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0025615	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0031274	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0100279	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0100282	ORPHA:810	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0000509	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0000554	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0000979	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001025	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001369	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001396	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001399	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001873	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001919	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0001937	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002090	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0002586	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0003201	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0005575	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0009830	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0012804	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0012819	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0025059	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0031368	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0031864	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0100806	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:810	Shigellosis		HP:0500006	ORPHA:810	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:851	Paris-Trousseau thrombocytopenia		HP:0001249	ORPHA:851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:851	Paris-Trousseau thrombocytopenia		HP:0001626	ORPHA:851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0000028	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0000046	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0000062	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0001522	ORPHA:168593	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0001695	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0002020	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0002045	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0002793	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0008736	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0010535	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0011675	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0012332	ORPHA:168593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0000602	ORPHA:168593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0001265	ORPHA:168593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0001336	ORPHA:168593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0001510	ORPHA:168593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168593	Sudden infant death-dysgenesis of the testes syndrome		HP:0001608	ORPHA:168593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0030057	ORPHA:562639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0032220	ORPHA:562639	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0000989	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0002910	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0003237	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0003493	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0011040	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0012378	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0033562	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034093	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034107	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034108	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034110	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034111	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034114	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034115	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0034155	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0100889	ORPHA:562639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0001394	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0001396	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0002037	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0002611	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0002829	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0002904	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0003155	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0003262	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0003496	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0025344	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0030167	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0030909	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0030948	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0030988	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0030991	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0032252	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0100279	ORPHA:562639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562639	Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome		HP:0030908	ORPHA:562639	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000348	ORPHA:93262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000956	ORPHA:93262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0002007	ORPHA:93262	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000238	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000248	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000262	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000272	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000316	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000327	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000405	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000453	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000486	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000508	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000520	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0001156	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0002308	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0002516	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0003312	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0005916	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0007360	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0100533	ORPHA:93262	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000174	ORPHA:93262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000444	ORPHA:93262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000505	ORPHA:93262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0000648	ORPHA:93262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0002076	ORPHA:93262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0002093	ORPHA:93262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93262	Crouzon syndrome-acanthosis nigricans syndrome		HP:0005107	ORPHA:93262	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000076	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000085	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000126	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000175	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000218	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000244	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000316	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000348	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000365	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000369	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000402	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000453	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000520	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0000646	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0001249	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0001250	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0001376	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0001601	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0001770	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0001773	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0002023	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0002098	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0002308	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0002410	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0002516	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0002566	ORPHA:93260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0002779	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0003196	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0005280	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0006101	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0008080	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0010059	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0010109	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0011304	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0011800	ORPHA:93260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93260	Pfeiffer syndrome type 3		HP:0200055	ORPHA:93260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001873	ORPHA:261323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000252	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000280	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000414	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000708	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001156	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001249	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001250	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001344	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001531	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001792	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001999	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0004322	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0006979	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0008872	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0008897	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0011344	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0012385	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0030084	ORPHA:261323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000179	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000219	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000311	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000316	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000319	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000369	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000403	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000463	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000486	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000494	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000678	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000752	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000958	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0000960	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001106	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001274	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001631	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0001903	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0002307	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0002465	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0002557	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0002714	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0002750	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0003086	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0003763	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0007874	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0008404	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0008551	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0008947	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0009226	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0009597	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0010230	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0011800	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0012172	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0012471	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0012745	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0030215	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0030799	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0100703	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261323	21q22.11q22.12 microdeletion syndrome		HP:0100716	ORPHA:261323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001290	ORPHA:2394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0002013	ORPHA:2394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0002151	ORPHA:2394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0003128	ORPHA:2394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0012758	ORPHA:2394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001250	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001254	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001257	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001943	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0002240	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0002480	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0002910	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0008344	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0011968	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0012402	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0100724	ORPHA:2394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0000252	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0000708	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001251	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001399	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001508	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001638	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0001987	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0003234	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0003394	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0007663	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0010913	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2394	Pyruvate dehydrogenase E3 deficiency		HP:0030872	ORPHA:2394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0000975	ORPHA:1063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0001903	ORPHA:1063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0011355	ORPHA:1063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0000329	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0000565	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0000967	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0000979	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0000998	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0001873	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0003401	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0005548	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0008069	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0010990	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0011900	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0012531	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1063	Tufted angioma		HP:0031490	ORPHA:1063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1062	Hereditary neurocutaneous malformation		HP:0000707	ORPHA:1062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1062	Hereditary neurocutaneous malformation		HP:0001028	ORPHA:1062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1062	Hereditary neurocutaneous malformation		HP:0001250	ORPHA:1062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1062	Hereditary neurocutaneous malformation		HP:0002277	ORPHA:1062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0000023	ORPHA:1069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0000028	ORPHA:1069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0000501	ORPHA:1069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0000508	ORPHA:1069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0000518	ORPHA:1069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0000526	ORPHA:1069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0001252	ORPHA:1069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1069	Aniridia-absent patella syndrome		HP:0006498	ORPHA:1069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1068	Aniridia-intellectual disability syndrome		HP:0000518	ORPHA:1068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1068	Aniridia-intellectual disability syndrome		HP:0000526	ORPHA:1068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1068	Aniridia-intellectual disability syndrome		HP:0000609	ORPHA:1068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1068	Aniridia-intellectual disability syndrome		HP:0001083	ORPHA:1068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1068	Aniridia-intellectual disability syndrome		HP:0002342	ORPHA:1068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000499	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000518	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000568	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000577	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0002788	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0007820	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0007957	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000506	ORPHA:2399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000589	ORPHA:2399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0001012	ORPHA:2399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000268	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000316	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000327	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000337	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000349	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000369	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000437	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000445	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0008850	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0009926	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0030670	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0030953	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0031111	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0040164	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0045075	ORPHA:2399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0000378	ORPHA:2399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0004209	ORPHA:2399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:0007633	ORPHA:2399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome		HP:3000022	ORPHA:2399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2399	Nasopalpebral lipoma-coloboma syndrome	NOT	HP:0002011	ORPHA:2399	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0000855	ORPHA:2398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0001012	ORPHA:2398	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0001288	ORPHA:2398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0001315	ORPHA:2398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0001387	ORPHA:2398	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0002240	ORPHA:2398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0002829	ORPHA:2398	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0003401	ORPHA:2398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0009124	ORPHA:2398	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2398	Multiple symmetric lipomatosis		HP:0009830	ORPHA:2398	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0000505	ORPHA:1067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0000508	ORPHA:1067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0000518	ORPHA:1067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0000545	ORPHA:1067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0001249	ORPHA:1067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0001596	ORPHA:1067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0001627	ORPHA:1067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0005599	ORPHA:1067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0007957	ORPHA:1067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0008053	ORPHA:1067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1067	Aniridia-ptosis-intellectual disability-familial obesity syndrome		HP:0009917	ORPHA:1067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0001249	ORPHA:281090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0001263	ORPHA:281090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0002381	ORPHA:281090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0007018	ORPHA:281090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0007957	ORPHA:281090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0000028	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0000083	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0000122	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0000135	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0000717	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0001250	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0001339	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0002488	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0002577	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0004298	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0004322	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0010866	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0100617	ORPHA:281090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0000962	ORPHA:281090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0000966	ORPHA:281090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281090	Syndromic recessive X-linked ichthyosis		HP:0008064	ORPHA:281090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0003010	ORPHA:849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0004406	ORPHA:849	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0000225	ORPHA:849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0000978	ORPHA:849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0004846	ORPHA:849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0030137	ORPHA:849	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0000132	ORPHA:849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0000979	ORPHA:849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0002239	ORPHA:849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0007420	ORPHA:849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0012587	ORPHA:849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0031364	ORPHA:849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0400008	ORPHA:849	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia		HP:0011871	ORPHA:849	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia	NOT	HP:0004866	ORPHA:849	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia	NOT	HP:0008148	ORPHA:849	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia	NOT	HP:0011870	ORPHA:849	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia	NOT	HP:0011872	ORPHA:849	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia	NOT	HP:0011894	ORPHA:849	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:849	Glanzmann thrombasthenia	NOT	HP:0031128	ORPHA:849	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0000298	ORPHA:1065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0000364	ORPHA:1065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0000526	ORPHA:1065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0001249	ORPHA:1065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0001251	ORPHA:1065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0001252	ORPHA:1065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0001263	ORPHA:1065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0002167	ORPHA:1065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0002168	ORPHA:1065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0004414	ORPHA:1065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1065	Aniridia-cerebellar ataxia-intellectual disability syndrome		HP:0100022	ORPHA:1065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001276	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001331	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001704	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002059	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002063	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002092	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002119	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002120	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002167	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002300	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002381	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002514	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002797	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0003552	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0004493	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0005306	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0007957	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0010529	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0010622	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0012062	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0012157	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0100761	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000943	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001269	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001650	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001679	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001680	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002301	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002445	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002652	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0002763	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000488	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000991	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001012	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001249	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001250	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001263	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001482	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001596	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0009125	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0012759	ORPHA:2396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000256	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000271	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000492	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000499	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000612	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000614	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000708	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0000929	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001052	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001257	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0001274	ORPHA:2396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0003470	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0011611	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2396	Encephalocraniocutaneous lipomatosis		HP:0040188	ORPHA:2396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0000122	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0000463	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0000486	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0000506	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0000526	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0001087	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0001363	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0002007	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0002714	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0004322	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0005280	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0011342	ORPHA:1064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0000347	ORPHA:1064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0001252	ORPHA:1064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0001334	ORPHA:1064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1064	Aniridia-renal agenesis-psychomotor retardation syndrome		HP:0007957	ORPHA:1064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001081	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001744	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001789	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001878	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001903	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001971	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0002863	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0004823	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0005507	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0010620	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0010978	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0100543	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0430028	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001935	ORPHA:846	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0011902	ORPHA:846	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001433	ORPHA:846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001635	ORPHA:846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001698	ORPHA:846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001923	ORPHA:846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0001978	ORPHA:846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0002202	ORPHA:846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0007430	ORPHA:846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:846	Alpha-thalassemia		HP:0000952	ORPHA:846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001324	ORPHA:845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002191	ORPHA:845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0003202	ORPHA:845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0003495	ORPHA:845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0010969	ORPHA:845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0012379	ORPHA:845	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000505	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000708	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000736	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001260	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001288	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001347	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002015	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002171	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002172	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002311	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002312	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002359	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002376	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002380	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002460	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0003394	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0003551	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0007010	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0007103	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0007340	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0009050	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0010729	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0011951	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0012696	ORPHA:845	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000496	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000618	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000648	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000709	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000716	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000739	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001250	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001272	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001290	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001310	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001332	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001336	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001337	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001344	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0001377	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002119	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002267	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002283	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002307	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002354	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002384	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0002540	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0003066	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0004302	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0004481	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0008959	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0009088	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0011147	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0011448	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0011471	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0012049	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0012515	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0100754	ORPHA:845	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000365	ORPHA:845	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0000826	ORPHA:845	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0003333	ORPHA:845	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0025013	ORPHA:845	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease		HP:0031358	ORPHA:845	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:845	Tay-Sachs disease	NOT	HP:0001433	ORPHA:845	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0000924	ORPHA:848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0000980	ORPHA:848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0001744	ORPHA:848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0001903	ORPHA:848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0001935	ORPHA:848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0011902	ORPHA:848	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0000044	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0000737	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0000929	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0001324	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0002093	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0002240	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0004349	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0004370	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0011031	ORPHA:848	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0001081	ORPHA:848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0001639	ORPHA:848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0001873	ORPHA:848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0004936	ORPHA:848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0012115	ORPHA:848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:848	Beta-thalassemia		HP:0200042	ORPHA:848	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000028	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000037	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000062	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000252	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000271	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000316	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000708	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001249	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002020	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002381	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0010461	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0011328	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0012368	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0012736	ORPHA:847	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000158	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000179	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000232	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000286	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000457	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000463	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000506	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000717	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001250	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001252	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001762	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0004322	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0008736	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0010804	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0010806	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0011800	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0011902	ORPHA:847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000010	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000077	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000126	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000164	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000407	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000545	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000618	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000648	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0000716	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001156	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001258	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001274	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001371	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001387	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001522	ORPHA:847	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0001903	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002017	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002019	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002120	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002251	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002383	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0002580	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0004209	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0008872	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0100022	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:847	X-linked alpha-thalassemia-intellectual disability syndrome		HP:0100716	ORPHA:847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0000218	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0000248	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0000316	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0000348	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0000365	ORPHA:93258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0000369	ORPHA:93258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0000520	ORPHA:93258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0001770	ORPHA:93258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0001773	ORPHA:93258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0002410	ORPHA:93258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0003196	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0004279	ORPHA:93258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0005280	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0006101	ORPHA:93258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0008080	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0009601	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0010059	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0010109	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0011304	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0011318	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93258	Pfeiffer syndrome type 1		HP:0011800	ORPHA:93258	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:841	Sebocystomatosis		HP:0000787	ORPHA:841	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:841	Sebocystomatosis		HP:0009720	ORPHA:841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:841	Sebocystomatosis		HP:0012035	ORPHA:841	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000175	ORPHA:93259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000218	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000238	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000272	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000316	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000348	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000369	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000413	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000453	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000520	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0000572	ORPHA:93259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0001249	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0001250	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0001263	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0001376	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0001601	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0001770	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0001773	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002023	ORPHA:93259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002098	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002308	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002410	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002516	ORPHA:93259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002566	ORPHA:93259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002676	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0002779	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0003196	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0005280	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0006101	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0008080	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0009603	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0010059	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0010109	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0011304	ORPHA:93259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93259	Pfeiffer syndrome type 2		HP:0200055	ORPHA:93259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000293	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000311	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000411	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000470	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000574	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001252	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001288	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001999	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002167	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002311	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002553	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002916	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0003312	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001382	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0012332	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0100543	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0100790	ORPHA:261318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000023	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000164	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000174	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000248	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000286	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000294	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000316	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000347	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000358	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000400	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000463	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000486	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000582	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001156	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001357	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001537	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001760	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001883	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002162	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002208	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002414	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0003196	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0003272	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0006101	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0100874	ORPHA:261318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000028	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000047	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000053	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000069	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000077	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000126	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000232	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000233	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000268	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000319	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000322	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000494	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000581	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000691	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0000926	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0001177	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002007	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002650	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002714	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0002808	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0003422	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0004349	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0004397	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0005562	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0006610	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0009738	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0030680	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0100490	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261318	Trisomy 20p syndrome		HP:0100542	ORPHA:261318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000726	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0001251	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0001260	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0001288	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0001310	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002066	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002080	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002120	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002354	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0030216	ORPHA:93256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000713	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000716	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000722	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000737	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000739	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000802	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0001265	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0001324	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002063	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002172	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002839	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0007340	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0009830	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0012083	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0012332	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0012534	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0100275	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0100515	ORPHA:93256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000821	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0000822	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0001300	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002015	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002067	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002363	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002607	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0002615	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93256	Fragile X-associated tremor/ataxia syndrome		HP:0003326	ORPHA:93256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:840	Syringocystadenoma papilliferum		HP:0001482	ORPHA:840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:840	Syringocystadenoma papilliferum		HP:0002209	ORPHA:840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:840	Syringocystadenoma papilliferum		HP:0008066	ORPHA:840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:840	Syringocystadenoma papilliferum		HP:0010815	ORPHA:840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:840	Syringocystadenoma papilliferum		HP:0200034	ORPHA:840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000750	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001249	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001252	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001510	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001518	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0002813	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0012520	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0012758	ORPHA:261311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000358	ORPHA:261311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000494	ORPHA:261311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000582	ORPHA:261311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001250	ORPHA:261311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001531	ORPHA:261311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0006385	ORPHA:261311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000047	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000233	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000286	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000297	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000316	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000319	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000325	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000341	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000414	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000460	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000520	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000729	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0000960	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001182	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001562	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001631	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001713	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001762	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001763	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0001822	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0002079	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0002188	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0002553	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0002573	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0002827	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0006709	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0009899	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0012304	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261311	20q13.33 microdeletion syndrome		HP:0012858	ORPHA:261311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0010785	ORPHA:180229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0030061	ORPHA:180229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0030338	ORPHA:180229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0002027	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0002585	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0005107	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0006254	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0012288	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0031500	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0040231	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0045026	ORPHA:180229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0000053	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0000818	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0000858	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0001945	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0003144	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0003270	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0008236	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:180229	Polyembryoma		HP:0030088	ORPHA:180229	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000286	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000347	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000501	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000518	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000568	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001305	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001541	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001561	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002119	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0003560	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0004322	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0007957	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0010880	ORPHA:1052	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000252	ORPHA:1052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000325	ORPHA:1052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000478	ORPHA:1052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000504	ORPHA:1052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001249	ORPHA:1052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001263	ORPHA:1052	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000003	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000062	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000175	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000340	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000348	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000365	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000358	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000445	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000457	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000494	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000821	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000924	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0000929	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001000	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001250	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001252	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001360	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001510	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001511	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001631	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001659	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001679	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001680	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0001682	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002007	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002101	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002104	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002247	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002664	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002667	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002797	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002817	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002859	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0002863	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0003003	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0004209	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0006721	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0007360	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0007370	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0007565	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0010978	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0012126	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0030680	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0100650	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1052	Mosaic variegated aneuploidy syndrome		HP:0200008	ORPHA:1052	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0001249	ORPHA:2382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0001298	ORPHA:2382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0011195	ORPHA:2382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0000708	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0000718	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0000729	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0000737	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0000752	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0001268	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0001336	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0002069	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0002353	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0002363	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0002527	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0007270	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0010818	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0010819	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0012075	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0012758	ORPHA:2382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0000709	ORPHA:2382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0000741	ORPHA:2382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0002123	ORPHA:2382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0002321	ORPHA:2382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0002376	ORPHA:2382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2382	Lennox-Gastaut syndrome		HP:0007359	ORPHA:2382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000309	ORPHA:1051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0012155	ORPHA:1051	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000283	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000316	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000491	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000579	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000582	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0001249	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0001525	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0001643	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0002007	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0002194	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0002251	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0003510	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0004325	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0005280	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0007663	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0007980	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0008619	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0011120	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0011220	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0012332	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0030491	ORPHA:1051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000160	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000217	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000343	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000452	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000463	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000533	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000620	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000670	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0000742	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0001631	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0002098	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0002209	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0004411	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0006979	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0008872	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0009890	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0010298	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0010782	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0011451	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0012450	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0012537	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0012804	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1051	Ramos-Arroyo syndrome		HP:0045025	ORPHA:1051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0000164	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0001373	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0002750	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0002829	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0003202	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0004322	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0010885	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2380	Legg-Calvé-Perthes disease		HP:0100773	ORPHA:2380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0000988	ORPHA:1059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0001048	ORPHA:1059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0001482	ORPHA:1059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0001928	ORPHA:1059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0001935	ORPHA:1059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0002580	ORPHA:1059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0002584	ORPHA:1059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0002597	ORPHA:1059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0002653	ORPHA:1059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0003010	ORPHA:1059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0005244	ORPHA:1059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0100026	ORPHA:1059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1059	Blue rubber bleb nevus		HP:0100761	ORPHA:1059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002072	ORPHA:2388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0004305	ORPHA:2388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000708	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001250	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001300	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001315	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001927	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002311	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002340	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002451	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002460	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002495	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002527	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003198	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003236	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003438	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003445	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003477	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003693	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0006956	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0007078	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012049	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0025402	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0030272	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0100034	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0100035	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0100295	ORPHA:2388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000496	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000514	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000643	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000712	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000716	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000718	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000722	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000736	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000737	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000739	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000741	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0000752	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001260	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001268	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001276	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001350	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001369	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001744	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001824	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002015	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002067	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002069	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002120	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002240	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002322	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002487	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002505	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002599	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003380	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0003763	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0004302	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0006913	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0008110	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0008767	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0009049	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0010808	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0011999	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012048	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012167	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012168	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012479	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012697	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0025100	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0025331	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0025479	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0025517	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0030220	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0031008	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0031843	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0031908	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0031982	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0100716	ORPHA:2388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0001644	ORPHA:2388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0002360	ORPHA:2388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012332	ORPHA:2388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0012675	ORPHA:2388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0025435	ORPHA:2388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0031956	ORPHA:2388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2388	Choreoacanthocytosis		HP:0031964	ORPHA:2388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0000498	ORPHA:2387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0000499	ORPHA:2387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0000613	ORPHA:2387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0000787	ORPHA:2387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0001231	ORPHA:2387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0005978	ORPHA:2387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0008388	ORPHA:2387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2387	Leukonychia totalis		HP:0009720	ORPHA:2387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:839	Congenital nephrotic syndrome, Finnish type		HP:0000091	ORPHA:839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:839	Congenital nephrotic syndrome, Finnish type		HP:0000093	ORPHA:839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:839	Congenital nephrotic syndrome, Finnish type		HP:0000100	ORPHA:839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:839	Congenital nephrotic syndrome, Finnish type		HP:0000696	ORPHA:839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:839	Congenital nephrotic syndrome, Finnish type		HP:0004639	ORPHA:839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1055	Congenital left ventricular aneurysm		HP:0001711	ORPHA:1055	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1055	Congenital left ventricular aneurysm		HP:0001635	ORPHA:1055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1055	Congenital left ventricular aneurysm		HP:0002104	ORPHA:1055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1055	Congenital left ventricular aneurysm		HP:0005135	ORPHA:1055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1055	Congenital left ventricular aneurysm		HP:0011675	ORPHA:1055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1055	Congenital left ventricular aneurysm		HP:0012249	ORPHA:1055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0000972	ORPHA:2386	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0001276	ORPHA:2386	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0002317	ORPHA:2386	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0100543	ORPHA:2386	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0000726	ORPHA:2386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0002200	ORPHA:2386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0002273	ORPHA:2386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0010845	ORPHA:2386	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0001324	ORPHA:2386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0001350	ORPHA:2386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0002312	ORPHA:2386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0030051	ORPHA:2386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0100252	ORPHA:2386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0200034	ORPHA:2386	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0002079	ORPHA:2386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2386	Leukoencephalopathy-palmoplantar keratoderma syndrome		HP:0003380	ORPHA:2386	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0002315	ORPHA:838	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000407	ORPHA:838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000572	ORPHA:838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0001273	ORPHA:838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0001289	ORPHA:838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0001290	ORPHA:838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0100543	ORPHA:838	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000360	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000496	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000651	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000708	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000709	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000741	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0000751	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0001254	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0001260	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0001324	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0002017	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0002066	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0002321	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0002493	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0003474	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:838	Susac syndrome		HP:0100851	ORPHA:838	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0011645	ORPHA:1054	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0001659	ORPHA:1054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0002094	ORPHA:1054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0030148	ORPHA:1054	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0000969	ORPHA:1054	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0001635	ORPHA:1054	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0012735	ORPHA:1054	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0001297	ORPHA:1054	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0006689	ORPHA:1054	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0100520	ORPHA:1054	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1054	Aneurysm of sinus of Valsalva		HP:0100749	ORPHA:1054	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1053	Vein of Galen aneurysmal malformation		HP:0002617	ORPHA:1053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1053	Vein of Galen aneurysmal malformation		HP:0100659	ORPHA:1053	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1053	Vein of Galen aneurysmal malformation		HP:0100784	ORPHA:1053	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0003005	ORPHA:251992	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0000834	ORPHA:251992	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0005220	ORPHA:251992	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0045026	ORPHA:251992	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0200063	ORPHA:251992	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0000822	ORPHA:251992	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0002574	ORPHA:251992	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0004390	ORPHA:251992	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0005249	ORPHA:251992	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0100631	ORPHA:251992	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0000315	ORPHA:251992	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0002034	ORPHA:251992	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0002239	ORPHA:251992	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0003330	ORPHA:251992	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0007110	ORPHA:251992	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251992	Ganglioneuroma		HP:0008775	ORPHA:251992	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0000093	ORPHA:834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0000100	ORPHA:834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0000639	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0000657	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001000	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001249	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001250	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001251	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001252	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001257	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001260	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001263	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001288	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001531	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001541	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001744	ORPHA:834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001760	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001789	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0001999	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0002167	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0002205	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0002240	ORPHA:834	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0002305	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0002652	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0002817	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0004349	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0007256	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0007730	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0010318	ORPHA:834	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:834	Free sialic acid storage disease		HP:0200042	ORPHA:834	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0000716	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0000739	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0000741	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0001300	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002019	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002063	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002067	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002172	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002310	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002322	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002359	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002494	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002530	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0004926	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0005341	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0007256	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0008652	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0010307	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0010536	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0012332	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0012658	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0012670	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0030015	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0030880	ORPHA:98933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0000640	ORPHA:98933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0001260	ORPHA:98933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002066	ORPHA:98933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002073	ORPHA:98933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0002174	ORPHA:98933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98933	Multiple system atrophy, parkinsonian type		HP:0100595	ORPHA:98933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0000751	ORPHA:98934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0100022	ORPHA:98934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0000708	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0000726	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0001288	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0001300	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0001332	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0001347	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0001824	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0002060	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0002072	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0002120	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0002340	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0002354	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0002476	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0004302	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0004305	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98934	Huntington disease-like 2		HP:0010994	ORPHA:98934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0000252	ORPHA:833	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0000293	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0000343	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0000490	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0000545	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0001083	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0001250	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0001251	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0001257	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0001285	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0002017	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0002376	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0002793	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0003196	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0003355	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0004374	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0008872	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0010864	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0011220	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0012471	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:833	Encephalopathy due to sulfite oxidase deficiency		HP:0100022	ORPHA:833	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0001993	ORPHA:832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:6000361	ORPHA:832	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0002013	ORPHA:832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0002789	ORPHA:832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0002919	ORPHA:832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0410175	ORPHA:832	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0001252	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0001254	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0001259	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0001531	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0001640	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0001944	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0002018	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:832	Succinyl-CoA:3-oxoacid CoA transferase deficiency		HP:0004325	ORPHA:832	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000233	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000252	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000316	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000322	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000347	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000348	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000400	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000414	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000431	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000490	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0000963	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0001010	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0001252	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0001256	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0001508	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0001511	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0001562	ORPHA:261304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0002098	ORPHA:261304	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0008070	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0010781	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0011343	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0011968	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0100578	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261304	Paternal 20q13.2q13.3 microdeletion syndrome		HP:0100840	ORPHA:261304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0001288	ORPHA:363454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0002460	ORPHA:363454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0002515	ORPHA:363454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0003391	ORPHA:363454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0003701	ORPHA:363454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0005853	ORPHA:363454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0008944	ORPHA:363454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0001265	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0001270	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0001347	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0001371	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0001385	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0001558	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0003307	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0005109	ORPHA:363454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0003547	ORPHA:363454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363454	BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy		HP:0030237	ORPHA:363454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0000464	ORPHA:1041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001518	ORPHA:1041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001541	ORPHA:1041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001790	ORPHA:1041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0005268	ORPHA:1041	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0030005	ORPHA:1041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0032548	ORPHA:1041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0000077	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001004	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001561	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001698	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001871	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0002202	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0007430	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0030680	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0032169	ORPHA:1041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0000079	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0001627	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0002652	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0002664	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0011024	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0011675	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0031110	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1041	Hydrops fetalis		HP:0100763	ORPHA:1041	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0000944	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0001387	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0002814	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0004039	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0004322	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0005930	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0006487	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0006501	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1040	Metaphyseal anadysplasia		HP:0040071	ORPHA:1040	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0000944	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0001156	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0001385	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0002644	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0002650	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0002652	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0003312	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0004209	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0004322	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0004349	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0005916	ORPHA:2370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0000520	ORPHA:2370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0001511	ORPHA:2370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0000160	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0000233	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0000358	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0000486	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0001263	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0001671	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0003196	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2370	Larsen-like osseous dysplasia-short stature syndrome		HP:0007957	ORPHA:2370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0000256	ORPHA:2379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0000486	ORPHA:2379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0001249	ORPHA:2379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0001250	ORPHA:2379	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0002007	ORPHA:2379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0002063	ORPHA:2379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0002167	ORPHA:2379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0002396	ORPHA:2379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2379	Early-onset parkinsonism-intellectual disability syndrome		HP:0100022	ORPHA:2379	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1048	Isolated anencephaly/exencephaly		HP:0002323	ORPHA:1048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1048	Isolated anencephaly/exencephaly		HP:0008207	ORPHA:1048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0000164	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0000168	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0000272	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0000490	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0000970	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0001058	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0001256	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0002661	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0007021	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0007249	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64752	Hereditary sensory and autonomic neuropathy type 5		HP:0010829	ORPHA:64752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0000750	ORPHA:163721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0001250	ORPHA:163721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0011098	ORPHA:163721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0001249	ORPHA:163721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0002307	ORPHA:163721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0007334	ORPHA:163721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0007359	ORPHA:163721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0011196	ORPHA:163721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0011198	ORPHA:163721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0031491	ORPHA:163721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0000736	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0001260	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0001328	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0001611	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0002079	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0002546	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0010300	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163721	Rolandic epilepsy-speech dyspraxia syndrome		HP:0031434	ORPHA:163721	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001177	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001199	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001770	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001841	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0005916	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0006101	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0008368	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0009601	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0010689	ORPHA:2378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0000366	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0000430	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0000448	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0000457	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001376	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001883	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0002000	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0003019	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0003974	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0009556	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0010503	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0100524	ORPHA:2378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0000028	ORPHA:2378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0000238	ORPHA:2378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0000316	ORPHA:2378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001249	ORPHA:2378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0001252	ORPHA:2378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0002714	ORPHA:2378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2378	Laurin-Sandrow syndrome		HP:0007370	ORPHA:2378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0001251	ORPHA:64753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0001284	ORPHA:64753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0006855	ORPHA:64753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0007141	ORPHA:64753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0000640	ORPHA:64753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0000657	ORPHA:64753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0001152	ORPHA:64753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0002141	ORPHA:64753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0003474	ORPHA:64753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0006254	ORPHA:64753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0000486	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0001266	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0001332	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0002015	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0002174	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0002346	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0002839	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0003073	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0003124	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0003236	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0003487	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64753	Spinocerebellar ataxia with axonal neuropathy type 2		HP:0007256	ORPHA:64753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000047	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000069	ORPHA:1046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000160	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000233	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000252	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000347	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000457	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0000929	ORPHA:1046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001252	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001541	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001561	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001562	ORPHA:1046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001744	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001852	ORPHA:1046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001903	ORPHA:1046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0001928	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0002093	ORPHA:1046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0006703	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0008678	ORPHA:1046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1046	Lethal hemolytic anemia-genital anomalies syndrome		HP:0008736	ORPHA:1046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0001161	ORPHA:2377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0001249	ORPHA:2377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0001513	ORPHA:2377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0006101	ORPHA:2377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0009896	ORPHA:2377	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000028	ORPHA:2377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000083	ORPHA:2377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000407	ORPHA:2377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0004322	ORPHA:2377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0008736	ORPHA:2377	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000248	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000286	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000358	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000486	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000518	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000612	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0000639	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0001156	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0001251	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0002612	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0005978	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0007598	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0030680	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2377	Laurence-Moon syndrome		HP:0100627	ORPHA:2377	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0010566	ORPHA:64754	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0025249	ORPHA:64754	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0000252	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0000518	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0001052	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0001250	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0001595	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0001760	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0001770	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0002414	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0002650	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0003298	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0003468	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0006101	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0008064	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64754	Nevus comedonicus syndrome		HP:0100258	ORPHA:64754	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0000045	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0000064	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0000767	ORPHA:64755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0000768	ORPHA:64755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0000902	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0001034	ORPHA:64755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0002558	ORPHA:64755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0002650	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0002808	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0002983	ORPHA:64755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0002992	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0003298	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0003724	ORPHA:64755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0005815	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0010311	ORPHA:64755	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0010566	ORPHA:64755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0100559	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0100560	ORPHA:64755	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64755	Becker nevus syndrome		HP:0100578	ORPHA:64755	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2375	Laryngeal abductor paralysis-intellectual disability syndrome		HP:0001605	ORPHA:2375	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2375	Laryngeal abductor paralysis-intellectual disability syndrome		HP:0002110	ORPHA:2375	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2375	Laryngeal abductor paralysis-intellectual disability syndrome		HP:0004886	ORPHA:2375	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2375	Laryngeal abductor paralysis-intellectual disability syndrome		HP:0000252	ORPHA:2375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2375	Laryngeal abductor paralysis-intellectual disability syndrome		HP:0001270	ORPHA:2375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2375	Laryngeal abductor paralysis-intellectual disability syndrome		HP:0002342	ORPHA:2375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2375	Laryngeal abductor paralysis-intellectual disability syndrome		HP:0012768	ORPHA:2375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2374	Isolated congenital laryngeal web		HP:0001601	ORPHA:2374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2374	Isolated congenital laryngeal web		HP:0001609	ORPHA:2374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2374	Isolated congenital laryngeal web		HP:0001671	ORPHA:2374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2374	Isolated congenital laryngeal web		HP:0002098	ORPHA:2374	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2374	Isolated congenital laryngeal web		HP:0004322	ORPHA:2374	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2374	Isolated congenital laryngeal web		HP:0010307	ORPHA:2374	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2373	Congenital laryngomalacia		HP:0000175	ORPHA:2373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2373	Congenital laryngomalacia		HP:0001601	ORPHA:2373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2373	Congenital laryngomalacia		HP:0001608	ORPHA:2373	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2373	Congenital laryngomalacia		HP:0100335	ORPHA:2373	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001265	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001270	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001558	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001776	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0002540	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0002804	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0008935	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0030200	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0430025	ORPHA:319332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0000028	ORPHA:319332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0002650	ORPHA:319332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0000276	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0000343	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0000400	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0000486	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001181	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001188	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001249	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0001518	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0003391	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0005191	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0005280	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0005469	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0008897	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0011471	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0012785	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita		HP:0031729	ORPHA:319332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita	NOT	HP:0000252	ORPHA:319332	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita	NOT	HP:0001561	ORPHA:319332	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:319332	Autosomal recessive myogenic arthrogryposis multiplex congenita	NOT	HP:0040081	ORPHA:319332	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0001942	ORPHA:31824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0001944	ORPHA:31824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0001974	ORPHA:31824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002013	ORPHA:31824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002018	ORPHA:31824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002098	ORPHA:31824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002615	ORPHA:31824	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0000083	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0001635	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0001871	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002014	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002148	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002900	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002901	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002902	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0002917	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0003111	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0003128	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0004360	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0004372	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0005521	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0006543	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0006846	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0011106	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0011675	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0012819	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0030149	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0100520	ORPHA:31824	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31824	Colchicine poisoning		HP:0001596	ORPHA:31824	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000164	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000348	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000490	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000750	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0001999	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0003189	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0009765	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0040196	ORPHA:363444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000010	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000119	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000278	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000286	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000319	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000670	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0001263	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0001627	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0002119	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0006989	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0010864	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0012443	ORPHA:363444	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000047	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000054	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000077	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000085	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000122	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000215	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000220	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000307	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000337	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000365	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0000689	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0001328	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0001631	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0001643	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0001845	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0002023	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0008209	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0009890	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0010282	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0011623	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0011682	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0012382	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0012385	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363444	THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome		HP:0030127	ORPHA:363444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0002721	ORPHA:538934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0001744	ORPHA:538934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0001876	ORPHA:538934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0001954	ORPHA:538934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0005229	ORPHA:538934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0012115	ORPHA:538934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0034799	ORPHA:538934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0100280	ORPHA:538934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0000083	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0000123	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0000554	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0001369	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0002037	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0002583	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0002719	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0004313	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0012219	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0030151	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0031292	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0031693	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0040218	ORPHA:538934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538934	X-linked lymphoproliferative disease due to XIAP deficiency		HP:0001399	ORPHA:538934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0000666	ORPHA:163727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0002268	ORPHA:163727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0002356	ORPHA:163727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0007104	ORPHA:163727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0007332	ORPHA:163727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0011295	ORPHA:163727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0012012	ORPHA:163727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163727	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome		HP:0001250	ORPHA:163727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0001942	ORPHA:31825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0000505	ORPHA:31825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0000622	ORPHA:31825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0000822	ORPHA:31825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0002170	ORPHA:31825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0003077	ORPHA:31825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0030955	ORPHA:31825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0031982	ORPHA:31825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0000587	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0000618	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0001259	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0001273	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0001289	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0001658	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0002013	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0002014	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0002027	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0002453	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0002500	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0005978	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0007146	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0012128	ORPHA:31825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0001250	ORPHA:31825	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0001342	ORPHA:31825	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0002339	ORPHA:31825	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0004754	ORPHA:31825	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0005291	ORPHA:31825	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0031422	ORPHA:31825	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31825	Methanol poisoning		HP:0100651	ORPHA:31825	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001942	ORPHA:31826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0003128	ORPHA:31826	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001251	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001289	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001350	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001649	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002013	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002018	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002329	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002789	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002901	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0031844	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0031962	ORPHA:31826	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0000083	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0000822	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0000961	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001259	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001635	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001657	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002153	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002315	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002615	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002793	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0004885	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0005110	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0005263	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0007695	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0030955	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0031273	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0100598	ORPHA:31826	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0000124	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0000602	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0000639	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0000790	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001250	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001298	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0001336	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002045	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0002181	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0008682	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0010628	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0011037	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0030157	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31826	Ethylene glycol poisoning		HP:0031910	ORPHA:31826	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0008131	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0008144	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0008369	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0010741	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0025238	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0030840	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0031051	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0031955	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0100662	ORPHA:563991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0001369	ORPHA:563991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0010885	ORPHA:563991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0010886	ORPHA:563991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563991	Osteochondrosis of the tarsal bone		HP:0100323	ORPHA:563991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0010866	ORPHA:2369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0011418	ORPHA:2369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0040064	ORPHA:2369	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000077	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000765	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000776	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000925	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001196	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001627	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001629	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001631	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001683	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002011	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0005257	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0006711	ORPHA:2369	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000175	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000238	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000316	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000431	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000453	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0000612	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001132	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001195	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001392	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001540	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001776	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0001839	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002084	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002143	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002242	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002323	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002414	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002475	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0002933	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0003298	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0004275	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0005280	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0006368	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0006496	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0007385	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0007957	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0008458	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0009775	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0010055	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0010242	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0010541	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0010554	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0100656	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2369	Limb body wall complex		HP:0410030	ORPHA:2369	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0001543	ORPHA:2368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0001511	ORPHA:2368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0010881	ORPHA:2368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0011432	ORPHA:2368	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0034207	ORPHA:2368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0001561	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0001562	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0001622	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0002566	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0002580	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0011100	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0031368	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2368	Gastroschisis		HP:0100016	ORPHA:2368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000069	ORPHA:1035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000218	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000348	ORPHA:1035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000358	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000444	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000463	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000486	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000494	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0000958	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001166	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001249	ORPHA:1035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001250	ORPHA:1035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001252	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001513	ORPHA:1035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001537	ORPHA:1035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001631	ORPHA:1035	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001852	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0002007	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0002353	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0002857	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0002983	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0004322	ORPHA:1035	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0001382	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1035	Beta-mercaptolactate cysteine disulfiduria		HP:0100720	ORPHA:1035	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0002151	ORPHA:2364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0003236	ORPHA:2364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0003542	ORPHA:2364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0000972	ORPHA:2364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0002913	ORPHA:2364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0003326	ORPHA:2364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0003394	ORPHA:2364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0003552	ORPHA:2364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0009020	ORPHA:2364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0000083	ORPHA:2364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2364	Glycogen storage disease due to lactate dehydrogenase deficiency		HP:0003201	ORPHA:2364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000164	ORPHA:2363	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000217	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000377	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000478	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000670	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000682	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001097	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0009926	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0010286	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0011297	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0011481	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0011482	ORPHA:2363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000369	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000378	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000405	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000407	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000410	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000495	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000508	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000668	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000691	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001092	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001096	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001159	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001172	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001770	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001999	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0002984	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0006101	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0006297	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0007656	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0007892	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0007925	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0009777	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0009778	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0009942	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0011496	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0012155	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0012804	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0030084	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0032107	ORPHA:2363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000028	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000076	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000089	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000126	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000193	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000202	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000347	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000453	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000458	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000577	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0000813	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001250	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001263	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001369	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0001643	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0002015	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0002164	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0002650	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0005349	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0008551	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0011487	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2363	Lacrimoauriculodentodigital syndrome		HP:0012108	ORPHA:2363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000112	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000121	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000212	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000682	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000684	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000705	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0006286	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0011073	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0031428	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0100530	ORPHA:1031	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000083	ORPHA:1031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0000805	ORPHA:1031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0003127	ORPHA:1031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0004727	ORPHA:1031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1031	Enamel-renal syndrome		HP:0012365	ORPHA:1031	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0006665	ORPHA:96334	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001263	ORPHA:96334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001561	ORPHA:96334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001999	ORPHA:96334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0006267	ORPHA:96334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0011968	ORPHA:96334	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000158	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000278	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000470	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000767	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000924	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001371	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001510	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001540	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001622	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002002	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002751	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002866	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002878	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0005257	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0005268	ORPHA:96334	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0005280	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0008551	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0008897	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0009826	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0011335	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0011823	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0012745	ORPHA:96334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000028	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000160	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000252	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000260	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000286	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000303	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000322	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000327	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000343	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000347	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000358	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000431	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000445	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000463	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000490	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000581	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000773	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000774	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000882	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000884	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000890	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000907	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000919	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000946	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000954	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0000973	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001181	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001220	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001250	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001252	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001339	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001357	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001433	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001520	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001538	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001539	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001601	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001615	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001629	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001631	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001639	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001792	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001840	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002007	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002057	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002089	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002091	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002092	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002240	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002307	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002557	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002645	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002650	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002673	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002694	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002884	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002937	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0002982	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0003049	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0003186	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0003241	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0004299	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0004322	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0004415	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0005054	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0005736	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0005989	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0006591	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0006610	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0007685	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0009600	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0009824	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0009832	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0009836	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0010034	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0010301	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0010561	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0010655	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0010804	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0011343	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0011344	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0011471	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0011824	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0012284	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0012303	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0012385	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0012428	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0012471	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0040024	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0100864	ORPHA:96334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001511	ORPHA:96334	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:96334	Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14		HP:0001548	ORPHA:96334	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001629	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001642	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001643	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001647	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001680	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001714	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0002079	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0002119	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0002608	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0003196	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0005280	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0010800	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0011220	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000505	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000708	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000750	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001249	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001263	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001270	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001627	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0007018	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0012443	ORPHA:284169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000293	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000483	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000486	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000718	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000739	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001250	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001319	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0002019	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0002360	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0011968	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0012745	ORPHA:284169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000358	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000365	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000414	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000453	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000490	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000494	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000540	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000545	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000567	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000646	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000664	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0000729	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion		HP:0001321	ORPHA:284169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:211067	Episodic ataxia type 5		HP:0000640	ORPHA:211067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:211067	Episodic ataxia type 5		HP:0001251	ORPHA:211067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:211067	Episodic ataxia type 5		HP:0001260	ORPHA:211067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:211067	Episodic ataxia type 5		HP:0002078	ORPHA:211067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:211067	Episodic ataxia type 5		HP:0002172	ORPHA:211067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:211067	Episodic ataxia type 5		HP:0002321	ORPHA:211067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0000132	ORPHA:397685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0000134	ORPHA:397685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0000141	ORPHA:397685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0000789	ORPHA:397685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0000876	ORPHA:397685	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0000938	ORPHA:397685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0000939	ORPHA:397685	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0012886	ORPHA:397685	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397685	Familial hyperprolactinemia		HP:0100829	ORPHA:397685	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000293	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000311	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000322	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000365	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000369	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000508	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0001249	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0001252	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0001999	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0002263	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0002714	ORPHA:284160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000347	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000348	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000430	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000445	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000470	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000486	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000494	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000581	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000647	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0001611	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0007957	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0010489	ORPHA:284160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000028	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000160	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000164	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000218	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000286	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000316	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000518	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000568	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0000964	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0004408	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0005916	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0006101	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0007370	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0007730	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0008736	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284160	8q21.11 microdeletion syndrome		HP:0100490	ORPHA:284160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0000272	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0000286	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0000297	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0000303	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0000729	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0000739	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0000752	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0001250	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0001263	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0001290	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0001321	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0002079	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0002342	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0002360	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0002553	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0008050	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0009088	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0012471	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0045075	ORPHA:521258	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521258	Xq25 microduplication syndrome		HP:0004322	ORPHA:521258	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001945	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002102	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002829	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002923	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0007514	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0010702	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0011838	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0020151	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0030880	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0033028	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0034076	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0034092	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0034093	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0100614	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0100661	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000093	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000988	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001369	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002020	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002094	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002206	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002960	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0003326	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0003565	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0005263	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0012378	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0100324	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0100749	ORPHA:809	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000217	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000709	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001097	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001386	ORPHA:809	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000112	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000155	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000365	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000716	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0000979	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001009	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001250	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001387	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001596	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001698	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001701	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001744	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001873	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001878	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0001882	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002092	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002239	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002315	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002716	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0002797	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0003010	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0003075	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0003115	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0006530	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0009830	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0010885	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0012050	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0012219	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0012578	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0012819	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0025300	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0030878	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0031857	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0033430	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0033834	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:809	Mixed connective tissue disease		HP:0100721	ORPHA:809	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0100730	ORPHA:2357	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0031983	ORPHA:2357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0045026	ORPHA:2357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0001945	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002031	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002090	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002094	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0003319	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0012735	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0031035	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0032016	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0032445	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0100749	ORPHA:2357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0000464	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0000775	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0001324	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0001637	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0001697	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002015	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002027	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002103	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002105	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002315	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002577	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002585	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0002699	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0003396	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0003401	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0003418	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0010766	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0030833	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0100712	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2357	Bronchogenic cyst		HP:0100750	ORPHA:2357	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002315	ORPHA:2356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0010576	ORPHA:2356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0032070	ORPHA:2356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000020	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000238	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000508	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000622	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000639	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000651	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000716	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000734	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000737	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000745	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000818	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0000933	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001123	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001250	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001269	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001288	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001293	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001317	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001350	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002018	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002027	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002138	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002176	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002273	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002308	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002321	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002354	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002385	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002460	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002540	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002839	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002936	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0003401	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0003418	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0003698	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0004396	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0005324	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0006824	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0007086	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0007291	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0007340	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0009745	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0010303	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0010628	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0011499	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0011868	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0012246	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0012514	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0012700	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0025331	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0025479	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0030215	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0032327	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0100754	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0100785	ORPHA:2356	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001249	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0001360	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002084	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0002664	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0012294	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0012758	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0032059	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0032169	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2356	Arachnoid cyst		HP:0100951	ORPHA:2356	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0000246	ORPHA:163703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0000708	ORPHA:163703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0001254	ORPHA:163703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0001699	ORPHA:163703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0001945	ORPHA:163703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0002315	ORPHA:163703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0002353	ORPHA:163703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0002376	ORPHA:163703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0002960	ORPHA:163703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0003326	ORPHA:163703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0007359	ORPHA:163703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163703	Febrile infection-related epilepsy syndrome		HP:0012735	ORPHA:163703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000077	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000708	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0001250	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002539	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0009716	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0009717	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0009719	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0011354	ORPHA:805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000107	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000716	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000717	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000718	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000729	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000752	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0001249	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0001328	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002133	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002360	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0007359	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0007449	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0008762	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0009594	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0009721	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0009729	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0010615	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0011097	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0012433	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0012469	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0012622	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0012758	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0012798	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0040030	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0100710	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0100716	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0200035	ORPHA:805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000083	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000739	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000822	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0001407	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002098	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002105	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002465	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0006772	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0007018	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0009718	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0010953	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0011947	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0100804	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0200040	ORPHA:805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0000113	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002666	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002878	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002893	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0002897	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0003774	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0004942	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0005584	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0008208	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0011029	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0012778	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0030405	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:805	Tuberous sclerosis complex		HP:0100570	ORPHA:805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0000501	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0000529	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0001089	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0007663	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0009918	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0011483	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0011489	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0012040	ORPHA:64734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0007818	ORPHA:64734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0007990	ORPHA:64734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0011484	ORPHA:64734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0011500	ORPHA:64734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0011525	ORPHA:64734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0025309	ORPHA:64734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0025358	ORPHA:64734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64734	Iridocorneal endothelial syndrome		HP:0001100	ORPHA:64734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000252	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000275	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000347	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000363	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000387	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000444	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000494	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000501	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0000682	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0001249	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0001363	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0001385	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0001511	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0001852	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0002209	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0002650	ORPHA:808	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0002750	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0004209	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0004322	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0004326	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0001382	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0007495	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0009804	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0010579	ORPHA:808	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0011342	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:808	Seckel syndrome		HP:0100543	ORPHA:808	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000499	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000505	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000548	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000556	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000574	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000613	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000639	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000648	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0000664	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0002208	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1021	Amaurosis-hypertrichosis syndrome		HP:0008499	ORPHA:1021	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0000713	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0000726	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0000738	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0001250	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0001276	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0001289	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0001300	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0001336	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0002120	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0002185	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0002354	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0002463	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0003791	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0012433	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0012759	ORPHA:1020	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0000734	ORPHA:1020	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0000504	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0000657	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0001249	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0001251	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0002186	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0002381	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0010525	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0010526	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0011446	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1020	Early-onset autosomal dominant Alzheimer disease		HP:0030219	ORPHA:1020	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000256	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000343	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000347	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000463	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000470	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000474	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000774	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0001773	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0001789	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0002007	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0002983	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0003196	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0003336	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0003498	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0003510	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0005716	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0006703	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0010306	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0012368	ORPHA:93298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000772	ORPHA:93298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0001537	ORPHA:93298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0001561	ORPHA:93298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0001762	ORPHA:93298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0100541	ORPHA:93298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0000476	ORPHA:93298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93298	Achondrogenesis type 1B		HP:0030680	ORPHA:93298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000256	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000343	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000347	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000463	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000470	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000474	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000774	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0001789	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0002007	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0002983	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0003196	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0003270	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0003336	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0003510	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0005716	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0006703	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0010306	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0012368	ORPHA:93299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0001537	ORPHA:93299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0001561	ORPHA:93299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0001773	ORPHA:93299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0002757	ORPHA:93299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0004279	ORPHA:93299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0006640	ORPHA:93299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0100541	ORPHA:93299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0000476	ORPHA:93299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93299	Achondrogenesis type 1A		HP:0030680	ORPHA:93299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0000138	ORPHA:64739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0000837	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0001007	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0001541	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0002017	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0002018	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0002027	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0002202	ORPHA:64739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0003270	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0007430	ORPHA:64739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0008675	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0011106	ORPHA:64739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0012398	ORPHA:64739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0030088	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0012886	ORPHA:64739	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0030005	ORPHA:64739	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64739	Ovarian hyperstimulation syndrome		HP:0100598	ORPHA:64739	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0003026	ORPHA:93296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0011849	ORPHA:93296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000201	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000478	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000773	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000774	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000946	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000969	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0002089	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0002652	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0002983	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0004322	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0004605	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0008788	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0008828	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0011800	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0030290	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0031096	ORPHA:93296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000365	ORPHA:93296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000518	ORPHA:93296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000541	ORPHA:93296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0000545	ORPHA:93296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0001132	ORPHA:93296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0004327	ORPHA:93296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93296	Achondrogenesis type 2		HP:0006543	ORPHA:93296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0007354	ORPHA:803	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002180	ORPHA:803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003324	ORPHA:803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0007373	ORPHA:803	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0000217	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0000708	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0000712	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0000716	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0000739	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0001257	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0001260	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0001347	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0001618	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0001824	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002015	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002094	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002307	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002380	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002878	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003202	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003394	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003470	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003484	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003487	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003693	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0007340	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0008955	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0012378	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0012473	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0012531	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0030192	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0030195	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0030196	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0030878	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0031993	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0100543	ORPHA:803	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0001308	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002145	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002313	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002360	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0002463	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0003376	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0004326	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0009027	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0012764	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0033683	ORPHA:803	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:803	Amyotrophic lateral sclerosis		HP:0025425	ORPHA:803	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000023	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000069	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000079	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000160	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000175	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000205	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000211	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000218	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000232	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000252	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000293	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000294	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000298	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000316	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000343	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000347	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000358	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000396	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000426	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000470	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000482	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000486	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000505	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000508	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000518	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000534	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000545	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000581	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000600	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000643	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000689	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000737	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000739	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000767	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000768	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000772	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000787	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000912	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000926	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000939	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0000944	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001083	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001239	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001249	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001265	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001276	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001288	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001324	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001385	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001387	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001522	ORPHA:800	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001537	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001557	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001561	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001601	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001618	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001620	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001621	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001762	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0001763	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002047	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002092	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002093	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002104	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002167	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002230	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002486	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002645	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002650	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002652	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002673	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002750	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002804	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002808	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002812	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002857	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0002983	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003042	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003044	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003179	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003198	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003202	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003236	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003273	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003306	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003307	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003326	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003457	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0003712	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0004322	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0004325	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0004326	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0005830	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0005930	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0006487	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0007018	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0007740	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0008056	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0008734	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0008872	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0009743	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0010508	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0010978	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0011001	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0011069	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0011675	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0012368	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0012544	ORPHA:800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0100569	ORPHA:800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0100612	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0100795	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:800	Schwartz-Jampel syndrome		HP:0100813	ORPHA:800	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0000232	ORPHA:1028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0000682	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0000684	ORPHA:1028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0000958	ORPHA:1028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0000962	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0000966	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0001231	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0001800	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0001806	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0002213	ORPHA:1028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0006286	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0006288	ORPHA:1028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0006482	ORPHA:1028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0009804	ORPHA:1028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1028	Amelo-onycho-hypohidrotic syndrome		HP:0011073	ORPHA:1028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0002155	ORPHA:444490	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0003077	ORPHA:444490	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0012238	ORPHA:444490	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0000660	ORPHA:444490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0001433	ORPHA:444490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0001735	ORPHA:444490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0002574	ORPHA:444490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0100027	ORPHA:444490	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0001013	ORPHA:444490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0001397	ORPHA:444490	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0001508	ORPHA:444490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0002017	ORPHA:444490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0004325	ORPHA:444490	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0000716	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0000726	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0000819	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0000952	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0002204	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0002354	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0009789	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome		HP:0100851	ORPHA:444490	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:444490	Familial chylomicronemia syndrome	NOT	HP:0004416	ORPHA:444490	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000648	ORPHA:411590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000709	ORPHA:411590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000716	ORPHA:411590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000726	ORPHA:411590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000729	ORPHA:411590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000739	ORPHA:411590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000819	ORPHA:411590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000026	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000377	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000501	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000823	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000863	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0001952	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0002073	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0002579	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0003477	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0008193	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0008527	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0010935	ORPHA:411590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0000821	ORPHA:411590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0002093	ORPHA:411590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411590	Wolfram-like syndrome		HP:0008850	ORPHA:411590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0000825	ORPHA:411593	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0000831	ORPHA:411593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0000855	ORPHA:411593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0002725	ORPHA:411593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0010702	ORPHA:411593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0030057	ORPHA:411593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0000956	ORPHA:411593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0001824	ORPHA:411593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0001958	ORPHA:411593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0002960	ORPHA:411593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0003162	ORPHA:411593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0005059	ORPHA:411593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411593	Insulin autoimmune syndrome		HP:0012051	ORPHA:411593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000175	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000256	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000260	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000369	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000470	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000773	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000774	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000907	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000926	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000946	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0000969	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0001156	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0001538	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0001561	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0001623	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0001631	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0001762	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0002763	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0003015	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0003174	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0003417	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0005026	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0005622	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0008178	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0008479	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0008890	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2347	Lethal Kniest-like dysplasia		HP:0012368	ORPHA:2347	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0001824	ORPHA:64741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0001945	ORPHA:64741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0002094	ORPHA:64741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0002105	ORPHA:64741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0002113	ORPHA:64741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0006532	ORPHA:64741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0012735	ORPHA:64741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0100528	ORPHA:64741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64741	Pulmonary blastoma		HP:0100749	ORPHA:64741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1014	Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome		HP:0000815	ORPHA:1014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1014	Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome		HP:0001256	ORPHA:1014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1014	Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome		HP:0007418	ORPHA:1014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000324	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000465	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000470	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000925	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0002162	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0004602	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0005640	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0005986	ORPHA:2345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000119	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000365	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000772	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000912	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0002315	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0002650	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0003043	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0003298	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0005988	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0030833	ORPHA:2345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000086	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0000175	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0001291	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0001629	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0002023	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0002414	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0030680	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0003416	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0004374	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0004397	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0005107	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0008678	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0030680	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0034980	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2345	Isolated Klippel-Feil syndrome		HP:0100543	ORPHA:2345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0008151	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0030146	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0030169	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0031015	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0000952	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0000989	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001405	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001541	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001873	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0002239	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0002480	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0002719	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0002904	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0002910	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0003073	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0011954	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0020136	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0020137	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0030242	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0100543	ORPHA:64743	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001402	ORPHA:64743	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001744	ORPHA:64743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001903	ORPHA:64743	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001409	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001882	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001892	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0001971	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0002040	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0003262	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64743	Hepatoportal sclerosis		HP:0006707	ORPHA:64743	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0000853	ORPHA:64744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0100646	ORPHA:64744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0000821	ORPHA:64744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0000872	ORPHA:64744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0025379	ORPHA:64744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0032069	ORPHA:64744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0032300	ORPHA:64744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0001605	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0002015	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0002777	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0002901	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0002960	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0005994	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0009798	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0100647	ORPHA:64744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0005200	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0011784	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0012503	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0030991	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0031281	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0032039	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0045026	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease		HP:0100732	ORPHA:64744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease	NOT	HP:0002664	ORPHA:64744	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:64744	IgG4-related thyroid disease	NOT	HP:0012393	ORPHA:64744	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0000989	ORPHA:64745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0001065	ORPHA:64745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0030350	ORPHA:64745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0030351	ORPHA:64745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0001036	ORPHA:64745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0004324	ORPHA:64745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0025474	ORPHA:64745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0030898	ORPHA:64745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0200037	ORPHA:64745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0001041	ORPHA:64745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0030899	ORPHA:64745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0030900	ORPHA:64745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0031248	ORPHA:64745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0031538	ORPHA:64745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0100872	ORPHA:64745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0000964	ORPHA:64745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0008066	ORPHA:64745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0025493	ORPHA:64745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy		HP:0030901	ORPHA:64745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy	NOT	HP:0031540	ORPHA:64745	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:64745	Pruritic urticarial papules and plaques of pregnancy	NOT	HP:0031541	ORPHA:64745	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0000704	ORPHA:2342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0000982	ORPHA:2342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0000670	ORPHA:2342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0000972	ORPHA:2342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0001166	ORPHA:2342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0001763	ORPHA:2342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0001805	ORPHA:2342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0001870	ORPHA:2342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0009771	ORPHA:2342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0000958	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0001288	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0001581	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0001803	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0005830	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0006323	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0012785	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2342	Haim-Munk syndrome		HP:0410027	ORPHA:2342	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0000825	ORPHA:276556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001985	ORPHA:276556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001988	ORPHA:276556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0012051	ORPHA:276556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0030796	ORPHA:276556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0031084	ORPHA:276556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0040299	ORPHA:276556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0000713	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0000980	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001069	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001520	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001649	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001962	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0002329	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0012759	ORPHA:276556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001254	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001279	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001325	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0001639	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0002133	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0002173	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0002240	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0002591	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0007185	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0011968	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276556	Hyperinsulinism due to UCP2 deficiency		HP:0031224	ORPHA:276556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0000653	ORPHA:1010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0000982	ORPHA:1010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0001597	ORPHA:1010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0002209	ORPHA:1010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0008404	ORPHA:1010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0045075	ORPHA:1010	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0000958	ORPHA:1010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0001807	ORPHA:1010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0004528	ORPHA:1010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0010491	ORPHA:1010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0011838	ORPHA:1010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0012785	ORPHA:1010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0032152	ORPHA:1010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0001041	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0001058	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0002223	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0002298	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0002435	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0009886	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0009900	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0031057	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0040189	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0100018	ORPHA:1010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0000613	ORPHA:1010	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1010	Autosomal dominant palmoplantar keratoderma and congenital alopecia		HP:0001250	ORPHA:1010	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0000653	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0000989	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0001041	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0002287	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0004552	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0007502	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0025084	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0032152	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0045059	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0045075	ORPHA:2340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0000498	ORPHA:2340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0000509	ORPHA:2340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0000613	ORPHA:2340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0000982	ORPHA:2340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0001047	ORPHA:2340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0001131	ORPHA:2340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2340	Keratosis follicularis spinulosa decalvans		HP:0008404	ORPHA:2340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000501	ORPHA:98976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0012040	ORPHA:98976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000485	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000557	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000613	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000643	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0001089	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0007765	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0007906	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0007957	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0009926	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0011490	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0025751	ORPHA:98976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000545	ORPHA:98976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000572	ORPHA:98976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0000646	ORPHA:98976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0007663	ORPHA:98976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0012803	ORPHA:98976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98976	Congenital glaucoma		HP:0100693	ORPHA:98976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0000505	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0000525	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0000587	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0000593	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0001138	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0007854	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0007906	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0007994	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0012108	ORPHA:98977	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0011003	ORPHA:98977	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0012511	ORPHA:98977	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0012796	ORPHA:98977	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0000603	ORPHA:98977	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0012636	ORPHA:98977	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98977	Juvenile glaucoma		HP:0025326	ORPHA:98977	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0011490	ORPHA:98973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0011491	ORPHA:98973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0000483	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0000646	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0007663	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0011483	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0012040	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0025358	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0032122	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0100692	ORPHA:98973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0000501	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0000565	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0000613	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0000622	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0000632	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0007906	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0007957	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0009918	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0200026	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98973	Posterior polymorphous corneal dystrophy		HP:0200065	ORPHA:98973	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0000158	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0000280	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0000821	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0000952	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0001288	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0001324	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0001537	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0002019	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0002167	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0002360	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0003198	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0003326	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0003712	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0004322	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2349	Muscular pseudohypertrophy-hypothyroidism syndrome		HP:0100543	ORPHA:2349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0002664	ORPHA:443167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0001909	ORPHA:443167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0002860	ORPHA:443167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0003006	ORPHA:443167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0012182	ORPHA:443167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0012254	ORPHA:443167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0045026	ORPHA:443167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0100757	ORPHA:443167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:443167	NUT midline carcinoma		HP:0012142	ORPHA:443167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0002015	ORPHA:1018	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0002031	ORPHA:1018	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0012718	ORPHA:1018	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0100751	ORPHA:1018	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000093	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000112	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000407	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000478	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000518	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000790	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0001508	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0002013	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0002020	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0002571	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0003262	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0006756	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0010460	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0012622	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0100749	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0100771	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0410281	ORPHA:1018	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000491	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0000545	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0001824	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0002094	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0002205	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0003774	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0006524	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0010450	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0010614	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0010784	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0011501	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0011951	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0012252	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0012735	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0030416	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0032141	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0040288	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1018	X-linked Alport syndrome-diffuse leiomyomatosis		HP:0100650	ORPHA:1018	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0000969	ORPHA:98974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0007663	ORPHA:98974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0007957	ORPHA:98974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0011488	ORPHA:98974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0011490	ORPHA:98974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0011491	ORPHA:98974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0000572	ORPHA:98974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0000662	ORPHA:98974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98974	Fuchs endothelial corneal dystrophy		HP:0030857	ORPHA:98974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000147	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000311	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000819	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000855	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000869	ORPHA:2348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000956	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000963	ORPHA:2348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0000991	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0001397	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0001597	ORPHA:2348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0001635	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0001639	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0001677	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0001733	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0001744	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0002155	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0002230	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0002240	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0002621	ORPHA:2348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0003198	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0003326	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0003635	ORPHA:2348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0003712	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0005339	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0006288	ORPHA:2348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0006824	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0008065	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0009125	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0012084	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0100578	ORPHA:2348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0100601	ORPHA:2348	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0100607	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0100658	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2348	Familial partial lipodystrophy, Dunnigan type		HP:0100820	ORPHA:2348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0001256	ORPHA:86909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0001326	ORPHA:86909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002069	ORPHA:86909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002123	ORPHA:86909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0007018	ORPHA:86909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0000718	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0000737	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0001263	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0001268	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0001336	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002311	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002376	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0007057	ORPHA:86909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0001112	ORPHA:86909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0001260	ORPHA:86909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002121	ORPHA:86909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002373	ORPHA:86909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002463	ORPHA:86909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0007207	ORPHA:86909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0010862	ORPHA:86909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86909	Myoclonic epilepsy of infancy		HP:0002301	ORPHA:86909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0003005	ORPHA:251937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0002315	ORPHA:251937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0010302	ORPHA:251937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0012377	ORPHA:251937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0100006	ORPHA:251937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0000141	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0000802	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0000845	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0000975	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0002363	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0002460	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0002650	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0003401	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0005616	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0007359	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0011749	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0011761	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0012503	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0030018	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0040086	ORPHA:251937	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0000726	ORPHA:251937	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0001262	ORPHA:251937	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0001317	ORPHA:251937	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0002591	ORPHA:251937	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0003396	ORPHA:251937	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251937	Gangliocytoma		HP:0006767	ORPHA:251937	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0009942	ORPHA:363417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0011297	ORPHA:363417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000164	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000668	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001090	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001156	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001249	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001263	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001510	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001566	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001999	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0006152	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0008625	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0009608	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0009944	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0009966	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0009970	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0011087	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0100266	ORPHA:363417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000160	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000311	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000327	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000347	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000369	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000517	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000592	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000648	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000677	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000691	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0000692	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001328	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0001773	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0002465	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0003196	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0004209	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0004279	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0004322	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0005037	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0008368	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0009466	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0010109	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0010554	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0011078	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0012795	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0040022	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0040159	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0100345	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363417	Temtamy preaxial brachydactyly syndrome		HP:0100347	ORPHA:363417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000252	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000262	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000316	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000358	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000400	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000448	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000545	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000582	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000682	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000924	ORPHA:1005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000962	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0000966	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0001156	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0001249	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0001387	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0001511	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0001596	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0002650	ORPHA:1005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0002808	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0002827	ORPHA:1005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0003422	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0003510	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0004209	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0004422	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0005048	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0005819	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0006101	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0001249	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0008064	ORPHA:1005	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0008070	ORPHA:1005	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0008388	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0008855	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0009738	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0009811	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1005	Alopecia-contractures-dwarfism-intellectual disability syndrome		HP:0011039	ORPHA:1005	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1003	Scalp defects-postaxial polydactyly syndrome		HP:0001362	ORPHA:1003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1003	Scalp defects-postaxial polydactyly syndrome		HP:0002084	ORPHA:1003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1003	Scalp defects-postaxial polydactyly syndrome		HP:0002209	ORPHA:1003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1003	Scalp defects-postaxial polydactyly syndrome		HP:0005696	ORPHA:1003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0000491	ORPHA:2334	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0000539	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0001104	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0007663	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0007750	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0007759	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0007990	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0011496	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0025348	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0032107	ORPHA:2334	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0000482	ORPHA:2334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0000518	ORPHA:2334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0000526	ORPHA:2334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0000589	ORPHA:2334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0006934	ORPHA:2334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2334	Autosomal dominant keratitis		HP:0007633	ORPHA:2334	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0004322	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0005280	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001382	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0006101	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0006610	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0007598	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0010049	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0010761	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0030680	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0045075	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0200055	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000003	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000256	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000405	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000470	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000717	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000722	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000733	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000776	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001601	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001679	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002021	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002360	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002667	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002779	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0007018	ORPHA:1001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000311	ORPHA:1001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001249	ORPHA:1001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001252	ORPHA:1001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001263	ORPHA:1001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0011800	ORPHA:1001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000233	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000252	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000430	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000463	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000490	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000582	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000708	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0000964	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001156	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001250	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001513	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001537	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001770	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0001773	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002007	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002209	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002553	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002558	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0002714	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0004209	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1001	2q37 microdeletion syndrome		HP:0004279	ORPHA:1001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000343	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000400	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000426	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000430	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000463	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000465	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000470	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000486	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000506	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000574	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000637	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000664	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000677	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000891	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000954	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0001263	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0001566	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0001572	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0002650	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000028	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000175	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000219	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000252	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000316	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000325	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0002750	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0002942	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0002948	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0004322	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0008513	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0010720	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0011842	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0011968	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0012725	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0040019	ORPHA:2332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0000311	ORPHA:2332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0001250	ORPHA:2332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0002353	ORPHA:2332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0004474	ORPHA:2332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2332	KBG syndrome		HP:0045017	ORPHA:2332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1000	Ocular albinism with late-onset sensorineural deafness		HP:0000407	ORPHA:1000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1000	Ocular albinism with late-onset sensorineural deafness		HP:0000486	ORPHA:1000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1000	Ocular albinism with late-onset sensorineural deafness		HP:0000505	ORPHA:1000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1000	Ocular albinism with late-onset sensorineural deafness		HP:0000613	ORPHA:1000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1000	Ocular albinism with late-onset sensorineural deafness		HP:0000639	ORPHA:1000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1000	Ocular albinism with late-onset sensorineural deafness		HP:0001107	ORPHA:1000	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001369	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001654	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001701	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001894	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001945	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001974	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0002014	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0002027	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0003073	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0003565	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0011227	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0012378	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0025525	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0025537	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0025538	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0030953	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0031042	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0031250	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0100643	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000508	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000737	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000952	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001082	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001287	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0001635	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0002017	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000093	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000509	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000988	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0002633	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0025289	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0025493	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0100776	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0100825	ORPHA:2331	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000206	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0000969	ORPHA:2331	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0002076	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0002829	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0004970	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0006530	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0006824	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0011658	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0011675	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0012115	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0012819	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2331	Kawasaki disease		HP:0100586	ORPHA:2331	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000053	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000147	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000218	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000252	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000303	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000316	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000365	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000454	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000455	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000470	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000486	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000494	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000540	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000739	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000767	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0000776	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0001182	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0001250	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0001252	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0004322	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0001537	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0001620	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0001956	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0001999	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0002342	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0002650	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0002788	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0004691	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0007018	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0007164	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0008070	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0009890	ORPHA:284180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0011343	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284180	Xp22.13p22.2 duplication syndrome		HP:0200055	ORPHA:284180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000154	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000183	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000256	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000347	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000369	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000407	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001260	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001349	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001762	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002069	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002123	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002197	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002307	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002804	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0006818	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0007024	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0011787	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0011968	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0012469	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0012650	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0410011	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:3000047	ORPHA:268940	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001250	ORPHA:268940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000565	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0000750	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001256	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001263	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001268	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001270	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001272	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0001285	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002119	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002200	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002342	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0002463	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0004302	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0007256	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0007359	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0007362	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0009878	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0010522	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0011099	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0012429	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268940	Bilateral polymicrogyria		HP:0100543	ORPHA:268940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001249	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001250	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001269	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0002510	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0002539	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0007010	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0007024	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0010818	ORPHA:268943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0000421	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0000505	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0000565	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0000750	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0000961	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001256	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001270	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001297	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001312	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001336	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001999	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0002104	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0002133	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0002384	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0002421	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0002533	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0004305	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0006548	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0007359	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0008610	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0008936	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0011344	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0012389	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0012469	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0012650	ORPHA:268943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0000252	ORPHA:268943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001335	ORPHA:268943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0001627	ORPHA:268943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268943	Unilateral polymicrogyria		HP:0040288	ORPHA:268943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0001028	ORPHA:2330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0001873	ORPHA:2330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0011900	ORPHA:2330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0000967	ORPHA:2330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0000979	ORPHA:2330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0005306	ORPHA:2330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0012329	ORPHA:2330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0000975	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0001875	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0001882	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0001903	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0001937	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0005520	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0008151	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0031207	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0100766	ORPHA:2330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0000998	ORPHA:2330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0001923	ORPHA:2330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0002027	ORPHA:2330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0002098	ORPHA:2330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0003270	ORPHA:2330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0008069	ORPHA:2330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2330	Kasabach-Merritt phenomenon		HP:0040213	ORPHA:2330	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0000707	ORPHA:466650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002047	ORPHA:466650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002018	ORPHA:466650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002315	ORPHA:466650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002321	ORPHA:466650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002789	ORPHA:466650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0011703	ORPHA:466650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0012378	ORPHA:466650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0030850	ORPHA:466650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001250	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001251	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001254	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001289	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001324	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001410	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001657	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001892	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002013	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002153	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002615	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002901	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002905	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0003128	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0003236	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0003256	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0003710	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0005135	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0012250	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0012417	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0030830	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0031258	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0031284	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0100520	ORPHA:466650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0000958	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0000970	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001399	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001873	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0001919	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0002480	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0003201	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466650	Exercise-induced malignant hyperthermia		HP:0005521	ORPHA:466650	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0001249	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0001250	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0001263	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0001269	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0002539	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0011099	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0011153	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0100308	ORPHA:268947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0001256	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0001268	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0002342	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0007018	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0007334	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0007377	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0012015	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0012018	ORPHA:268947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0000020	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0000718	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0000758	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0001335	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0002354	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0002384	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0002463	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0007010	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0007229	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0011171	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0012014	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0012016	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268947	Unilateral focal polymicrogyria		HP:0012017	ORPHA:268947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0007968	ORPHA:91495	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000518	ORPHA:91495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000555	ORPHA:91495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000568	ORPHA:91495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0007663	ORPHA:91495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0007957	ORPHA:91495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000519	ORPHA:91495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0007917	ORPHA:91495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0009917	ORPHA:91495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0012109	ORPHA:91495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0030743	ORPHA:91495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0030744	ORPHA:91495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000482	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000486	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000557	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000594	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000618	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000646	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0000667	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0001104	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0008052	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0009926	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0011885	ORPHA:91495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:91495	Persistent hyperplastic primary vitreous		HP:0010766	ORPHA:91495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0000164	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0000230	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0000238	ORPHA:1008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0000365	ORPHA:1008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0000499	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0000704	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0000995	ORPHA:1008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0001250	ORPHA:1008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0001256	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0002209	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0002231	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0002289	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0002353	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1008	Alopecia-epilepsy-pyorrhea-intellectual disability syndrome		HP:0002354	ORPHA:1008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2339	Keratosis follicularis-dwarfism-cerebral atrophy syndrome		HP:0000252	ORPHA:2339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2339	Keratosis follicularis-dwarfism-cerebral atrophy syndrome		HP:0000561	ORPHA:2339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2339	Keratosis follicularis-dwarfism-cerebral atrophy syndrome		HP:0002059	ORPHA:2339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2339	Keratosis follicularis-dwarfism-cerebral atrophy syndrome		HP:0002223	ORPHA:2339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2339	Keratosis follicularis-dwarfism-cerebral atrophy syndrome		HP:0003510	ORPHA:2339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2339	Keratosis follicularis-dwarfism-cerebral atrophy syndrome		HP:0007439	ORPHA:2339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0000405	ORPHA:1006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0000499	ORPHA:1006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0002167	ORPHA:1006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0002205	ORPHA:1006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0002231	ORPHA:1006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0002721	ORPHA:1006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0004313	ORPHA:1006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0004322	ORPHA:1006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0008070	ORPHA:1006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0011073	ORPHA:1006	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1006	Alopecia antibody deficiency		HP:0100840	ORPHA:1006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0000975	ORPHA:2337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0007447	ORPHA:2337	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0000989	ORPHA:2337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0008066	ORPHA:2337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0010783	ORPHA:2337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0032259	ORPHA:2337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0032541	ORPHA:2337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0200034	ORPHA:2337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0200042	ORPHA:2337	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2337	Diffuse palmoplantar keratoderma, Bothnian type		HP:0001807	ORPHA:2337	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0000137	ORPHA:314473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0001541	ORPHA:314473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0002027	ORPHA:314473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0002202	ORPHA:314473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0002586	ORPHA:314473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0002671	ORPHA:314473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0003270	ORPHA:314473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0008703	ORPHA:314473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0010603	ORPHA:314473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0010618	ORPHA:314473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314473	Ovarian fibroma		HP:0030451	ORPHA:314473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002448	ORPHA:363400	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0000842	ORPHA:363400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0000855	ORPHA:363400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0003758	ORPHA:363400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0007272	ORPHA:363400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0009064	ORPHA:363400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0025128	ORPHA:363400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0100543	ORPHA:363400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0000280	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0000750	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001250	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001251	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001257	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001336	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001337	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001347	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001348	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001397	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002155	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002311	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002360	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0007256	ORPHA:363400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0000752	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0000822	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0000956	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0001394	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002059	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002066	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002230	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002240	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002273	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002340	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002451	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002529	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002878	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0003198	ORPHA:363400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363400	Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome		HP:0002133	ORPHA:363400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90160	Pressure-induced localized lipoatrophy		HP:0100578	ORPHA:90160	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90160	Pressure-induced localized lipoatrophy		HP:0003758	ORPHA:90160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90160	Pressure-induced localized lipoatrophy		HP:0011356	ORPHA:90160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90160	Pressure-induced localized lipoatrophy		HP:0007485	ORPHA:90160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90160	Pressure-induced localized lipoatrophy		HP:0010783	ORPHA:90160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90160	Pressure-induced localized lipoatrophy		HP:0011123	ORPHA:90160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90160	Pressure-induced localized lipoatrophy		HP:0200036	ORPHA:90160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0000013	ORPHA:325124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0000042	ORPHA:325124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0000054	ORPHA:325124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0000062	ORPHA:325124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0000837	ORPHA:325124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0008716	ORPHA:325124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0010469	ORPHA:325124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0012870	ORPHA:325124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0012872	ORPHA:325124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0040171	ORPHA:325124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325124	Testicular agenesis		HP:0100779	ORPHA:325124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0000271	ORPHA:2325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0000303	ORPHA:2325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0000322	ORPHA:2325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0000365	ORPHA:2325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0000545	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0000682	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0000684	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0001083	ORPHA:2325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0001231	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0001596	ORPHA:2325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0001800	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0001903	ORPHA:2325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0002209	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0003473	ORPHA:2325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0008066	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0009804	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0100543	ORPHA:2325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0100797	ORPHA:2325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2325	Epidermolysis bullosa simplex with anodontia/hypodontia		HP:0100798	ORPHA:2325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0100578	ORPHA:90158	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0003758	ORPHA:90158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0007485	ORPHA:90158	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0000953	ORPHA:90158	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0000989	ORPHA:90158	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0001010	ORPHA:90158	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0010783	ORPHA:90158	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0011123	ORPHA:90158	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0012344	ORPHA:90158	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0040189	ORPHA:90158	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90158	Idiopathic localized lipodystrophy		HP:0100324	ORPHA:90158	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0100578	ORPHA:90159	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0003758	ORPHA:90159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0007485	ORPHA:90159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0010701	ORPHA:90159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0010783	ORPHA:90159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0011123	ORPHA:90159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0200036	ORPHA:90159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0003493	ORPHA:90159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90159	Panniculitis-induced localized lipodystrophy		HP:0200029	ORPHA:90159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000316	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000750	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000938	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0001290	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0002007	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0002194	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0002209	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0002213	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0002757	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0004482	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0001382	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0008897	ORPHA:2324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000303	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000369	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000414	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000592	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0000954	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0001250	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0001757	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0002750	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0004691	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2324	Osteopenia-intellectual disability-sparse hair syndrome		HP:0011800	ORPHA:2324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000028	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000164	ORPHA:2323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000233	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000252	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000343	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000347	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000348	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000358	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000444	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000483	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000490	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000682	ORPHA:2323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000829	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0001249	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0001250	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0001773	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0002119	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0002205	ORPHA:2323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0002750	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0002901	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0002905	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0003198	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0003416	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0004322	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0005214	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0005280	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0005374	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0005686	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0007957	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0008056	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0008198	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0000377	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0008736	ORPHA:2323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0008846	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0008897	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2323	Sanjad-Sakati syndrome		HP:0200055	ORPHA:2323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000508	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000637	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000659	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000668	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000687	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000691	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001212	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001252	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001373	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001382	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001508	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001627	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001671	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001680	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002119	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002120	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002650	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002719	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0004322	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0006482	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0008947	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0010314	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0011968	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0025186	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0031087	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0410030	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000028	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000047	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000074	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000081	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000126	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000384	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000482	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000589	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000592	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000639	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000729	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000776	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000826	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000998	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001156	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001250	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001513	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001631	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002020	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000356	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000400	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000411	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000527	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0001249	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002000	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002553	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002937	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0003312	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0003316	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0005338	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0005819	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0007477	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0007655	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0008428	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0008897	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0009237	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0012758	ORPHA:2322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000079	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000164	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000175	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000202	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000218	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000238	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000252	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000389	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000405	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002353	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002720	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0002827	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0004209	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0004736	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0008678	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0008736	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0030001	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0034323	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0100267	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0100542	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0200055	ORPHA:2322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000568	ORPHA:2322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000609	ORPHA:2322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000825	ORPHA:2322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0012732	ORPHA:2322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0030434	ORPHA:2322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000407	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000437	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2322	Kabuki syndrome		HP:0000486	ORPHA:2322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000078	ORPHA:2321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000252	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000311	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000431	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000506	ORPHA:2321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000821	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000929	ORPHA:2321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0000958	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0001249	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0001252	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0001321	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0002162	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0002205	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0002777	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0003312	ORPHA:2321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0005280	ORPHA:2321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2321	Jung syndrome		HP:0007370	ORPHA:2321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0000952	ORPHA:70567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0000989	ORPHA:70567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0001945	ORPHA:70567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0002027	ORPHA:70567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0002039	ORPHA:70567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0011985	ORPHA:70567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0012378	ORPHA:70567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70567	Cholangiocarcinoma		HP:0100574	ORPHA:70567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0001608	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0001824	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0001945	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0002716	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0004396	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0012378	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0025267	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0030166	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0033050	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0033834	ORPHA:70568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0002014	ORPHA:70568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0002027	ORPHA:70568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0002239	ORPHA:70568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0003073	ORPHA:70568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0012115	ORPHA:70568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70568	Post-transplant lymphoproliferative disease		HP:0033608	ORPHA:70568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0000653	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0000952	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0001396	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0001744	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0002209	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0002231	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0002240	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0004552	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0008064	ORPHA:59303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0000668	ORPHA:59303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0000677	ORPHA:59303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0000682	ORPHA:59303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0000956	ORPHA:59303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59303	Neonatal ichthyosis-sclerosing cholangitis syndrome		HP:0001409	ORPHA:59303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000164	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000218	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000239	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000365	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000518	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000520	ORPHA:90153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000534	ORPHA:90153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000561	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000855	ORPHA:90153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000953	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0000963	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0001252	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0001371	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0001376	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0001596	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0001870	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0002645	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0002797	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0002829	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0003011	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0003077	ORPHA:90153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0004322	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0004334	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0005328	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0006710	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0007495	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0009839	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0009882	ORPHA:90153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0100679	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90153	Mandibuloacral dysplasia with type A lipodystrophy		HP:0100783	ORPHA:90153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0000825	ORPHA:276575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0000842	ORPHA:276575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001985	ORPHA:276575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0003162	ORPHA:276575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0030796	ORPHA:276575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0031084	ORPHA:276575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0040299	ORPHA:276575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0000713	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0000980	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001069	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001520	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001649	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001962	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0002173	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0002329	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0012759	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0031223	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0031224	ORPHA:276575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001254	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001279	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001325	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0001639	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0002133	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0002240	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0002591	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0007185	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0011968	ORPHA:276575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276575	Autosomal dominant hyperinsulinism due to SUR1 deficiency		HP:0100651	ORPHA:276575	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000160	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000164	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000239	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000347	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000444	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000520	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000823	ORPHA:90154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000855	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000924	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000953	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0000963	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001211	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001595	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001596	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0001870	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0002797	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003077	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003196	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0003761	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0004322	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0004334	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0005328	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0006710	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0007495	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0008404	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0009064	ORPHA:90154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0009839	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90154	Mandibuloacral dysplasia with type B lipodystrophy		HP:0009882	ORPHA:90154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0000252	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0000320	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0000340	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0000414	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0000444	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0001510	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0001873	ORPHA:169079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0001888	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0001903	ORPHA:169079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0002718	ORPHA:169079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0002721	ORPHA:169079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0002960	ORPHA:169079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0004313	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0004429	ORPHA:169079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0005403	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169079	Cernunnos-XLF deficiency		HP:0010976	ORPHA:169079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000202	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000358	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000369	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000414	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000480	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000568	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000612	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0001249	ORPHA:2328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000059	ORPHA:2328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000470	ORPHA:2328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0001508	ORPHA:2328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0002019	ORPHA:2328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0002566	ORPHA:2328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0008736	ORPHA:2328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000384	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0000413	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0001302	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0001629	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0001636	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0001643	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0002126	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2328	Kapur-Toriello syndrome		HP:0006989	ORPHA:2328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0100578	ORPHA:90156	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0003758	ORPHA:90156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0007485	ORPHA:90156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0000765	ORPHA:90156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0002840	ORPHA:90156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0010783	ORPHA:90156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0011123	ORPHA:90156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0040189	ORPHA:90156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0001596	ORPHA:90156	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90156	Centrifugal lipodystrophy		HP:0005320	ORPHA:90156	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90157	Drug-induced localized lipodystrophy		HP:0100578	ORPHA:90157	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90157	Drug-induced localized lipodystrophy		HP:0003758	ORPHA:90157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90157	Drug-induced localized lipodystrophy		HP:0007485	ORPHA:90157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90157	Drug-induced localized lipodystrophy		HP:0000953	ORPHA:90157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90157	Drug-induced localized lipodystrophy		HP:0001010	ORPHA:90157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90157	Drug-induced localized lipodystrophy		HP:0010783	ORPHA:90157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0000137	ORPHA:314478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0001007	ORPHA:314478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0001541	ORPHA:314478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0002027	ORPHA:314478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0002202	ORPHA:314478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0002586	ORPHA:314478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0003117	ORPHA:314478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0003270	ORPHA:314478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0006756	ORPHA:314478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0008703	ORPHA:314478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0010618	ORPHA:314478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0030088	ORPHA:314478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0030126	ORPHA:314478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0100244	ORPHA:314478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314478	Ovarian fibrothecoma		HP:0100608	ORPHA:314478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000044	ORPHA:2326	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0001249	ORPHA:2326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0010632	ORPHA:2326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000054	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000104	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000175	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000200	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000407	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000823	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000938	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000939	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0000961	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0001510	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0001644	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0001719	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0002750	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0004322	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0004971	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0008689	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0008734	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0010633	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0011638	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0012020	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0030148	ORPHA:2326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0001635	ORPHA:2326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0001653	ORPHA:2326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0001659	ORPHA:2326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0005211	ORPHA:2326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2326	Kallmann syndrome-heart disease syndrome		HP:0010444	ORPHA:2326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0000825	ORPHA:276580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0000842	ORPHA:276580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001985	ORPHA:276580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0003162	ORPHA:276580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0030796	ORPHA:276580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0031084	ORPHA:276580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0000713	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0000980	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001069	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001520	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001649	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001962	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0002173	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0002329	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0004924	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0012759	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0031224	ORPHA:276580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001254	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001279	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001324	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001325	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0001639	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0002133	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0002240	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0002591	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0007185	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0009800	ORPHA:276580	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0011968	ORPHA:276580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276580	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency		HP:0100651	ORPHA:276580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0002070	ORPHA:363432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0002078	ORPHA:363432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0000640	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0000666	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0001290	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0002167	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0001288	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0004302	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0006855	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0012444	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363432	Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency		HP:0100543	ORPHA:363432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0000238	ORPHA:251915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0000651	ORPHA:251915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0002017	ORPHA:251915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0002315	ORPHA:251915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0002354	ORPHA:251915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0002516	ORPHA:251915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0000492	ORPHA:251915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0000639	ORPHA:251915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0002131	ORPHA:251915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0002922	ORPHA:251915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0030531	ORPHA:251915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0100543	ORPHA:251915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0000364	ORPHA:251915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251915	Papillary tumor of the pineal region		HP:0001288	ORPHA:251915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000076	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000110	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000126	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000256	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000268	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000272	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000286	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000293	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000307	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000365	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000400	ORPHA:48652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000414	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000431	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000486	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000490	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000508	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000527	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000540	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000574	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000678	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000689	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000729	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000750	ORPHA:48652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000752	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000960	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0000966	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001004	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001176	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001249	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001250	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001263	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001274	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001319	ORPHA:48652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001513	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001537	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001581	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0001800	ORPHA:48652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0002017	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0002020	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0002360	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0002721	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0003763	ORPHA:48652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0004209	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0005616	ORPHA:48652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0007328	ORPHA:48652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0008278	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0011968	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0012167	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0012787	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0100540	ORPHA:48652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48652	Phelan-McDermid syndrome		HP:0100702	ORPHA:48652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002726	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002728	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002757	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0001382	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0006532	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0008391	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0011220	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0012735	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0025419	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0031292	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0031690	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0200034	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0001363	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0001945	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002617	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002665	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002754	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0007099	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0100658	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0200037	ORPHA:2314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000964	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000988	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000989	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002205	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002719	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0003212	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0011354	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0100750	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0200042	ORPHA:2314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000164	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000175	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000230	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000271	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000303	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000324	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000389	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000431	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000490	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000684	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000703	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000938	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0000939	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0001114	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0001595	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0001818	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0001880	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002020	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002110	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2314	Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency		HP:0002650	ORPHA:2314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000470	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000772	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000902	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0001511	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0002093	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0002650	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0003312	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0003422	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0004322	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0005108	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0006655	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0010306	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0010978	ORPHA:2311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0002808	ORPHA:2311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000008	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000023	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000028	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000047	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000069	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000175	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000252	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000256	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000269	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000337	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000343	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000358	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000463	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0000776	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0001249	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0001537	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0002435	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0003298	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0005280	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0006101	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0010772	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0030680	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0100490	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2311	Autosomal recessive spondylocostal dysostosis		HP:0100589	ORPHA:2311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0000505	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0000518	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0002023	ORPHA:2310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0002650	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0002814	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0002823	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0003307	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0005930	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2310	Absence deformity of leg-cataract syndrome		HP:0009816	ORPHA:2310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000506	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000639	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001053	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001100	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001249	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001250	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001251	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001252	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001257	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001263	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002019	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002027	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002251	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002595	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0007256	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0009830	ORPHA:163746	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000135	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000426	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000430	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000431	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000534	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000633	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000635	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000664	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002211	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002216	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0004388	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0005599	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0006978	ORPHA:163746	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0000966	ORPHA:163746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001337	ORPHA:163746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0001744	ORPHA:163746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002240	ORPHA:163746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0002804	ORPHA:163746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0011675	ORPHA:163746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163746	Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease		HP:0012332	ORPHA:163746	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000252	ORPHA:2319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000445	ORPHA:2319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0001511	ORPHA:2319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0003510	ORPHA:2319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000047	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000085	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000202	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000316	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000534	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000772	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0001167	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0001249	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0001765	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0001770	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0002553	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0002650	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0002974	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0002984	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0003019	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0003468	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0005916	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0009778	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0009811	ORPHA:2319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0000508	ORPHA:2319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0001305	ORPHA:2319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2319	Juberg-Hayward syndrome		HP:0001545	ORPHA:2319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000112	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000556	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001249	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001251	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001252	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001263	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001320	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002104	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002419	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002789	ORPHA:2318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000276	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000358	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000505	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000508	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000567	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000612	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000618	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000639	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000708	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000729	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0004422	ORPHA:2318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000083	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000238	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000426	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000463	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000486	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0000864	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001161	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001250	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0001829	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002084	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002251	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002269	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002553	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0002650	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0007370	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2318	Joubert syndrome with oculorenal defect		HP:0030680	ORPHA:2318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000135	ORPHA:2316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000405	ORPHA:2316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000413	ORPHA:2316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0001596	ORPHA:2316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0008070	ORPHA:2316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000324	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000411	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000561	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000670	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0001249	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0002223	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0003510	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0008551	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0010628	ORPHA:2316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000175	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000232	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000252	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000414	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000453	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000458	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000494	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0000966	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0001161	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0001177	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0001508	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0001636	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2316	Johnson neuroectodermal syndrome		HP:0007565	ORPHA:2316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000164	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000430	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001508	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001511	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001596	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001732	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001738	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0002024	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0003196	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0004322	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0010720	ORPHA:2315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000142	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000407	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000632	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000677	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000684	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000691	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001092	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001249	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001545	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001903	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0002023	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0002750	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0003075	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0010460	ORPHA:2315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000047	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000126	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000252	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000819	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0000969	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001252	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001522	ORPHA:2315	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001651	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0001671	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0005288	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0008736	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2315	Johanson-Blizzard syndrome		HP:0030680	ORPHA:2315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:211017	Spinocerebellar ataxia type 30		HP:0001260	ORPHA:211017	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:211017	Spinocerebellar ataxia type 30		HP:0002066	ORPHA:211017	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:211017	Spinocerebellar ataxia type 30		HP:0002070	ORPHA:211017	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:211017	Spinocerebellar ataxia type 30		HP:0000640	ORPHA:211017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:211017	Spinocerebellar ataxia type 30		HP:0002395	ORPHA:211017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:211017	Spinocerebellar ataxia type 30		HP:0006855	ORPHA:211017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50942	Striate palmoplantar keratoderma		HP:0000982	ORPHA:50942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50942	Striate palmoplantar keratoderma		HP:0001595	ORPHA:50942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50942	Striate palmoplantar keratoderma		HP:0001597	ORPHA:50942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50943	Keratolytic winter erythema		HP:0000975	ORPHA:50943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50943	Keratolytic winter erythema		HP:0010783	ORPHA:50943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50943	Keratolytic winter erythema		HP:0200039	ORPHA:50943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0010799	ORPHA:251909	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0002315	ORPHA:251909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0000708	ORPHA:251909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0002344	ORPHA:251909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0002354	ORPHA:251909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0002516	ORPHA:251909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0100543	ORPHA:251909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0000619	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0000763	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0001085	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0001250	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0003470	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0007045	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0007663	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0007987	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0009919	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0100576	ORPHA:251909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0001254	ORPHA:251909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251909	Pineoblastoma		HP:0004372	ORPHA:251909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0000968	ORPHA:50944	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0000982	ORPHA:50944	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0007380	ORPHA:50944	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0008070	ORPHA:50944	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0000668	ORPHA:50944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0001596	ORPHA:50944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0006323	ORPHA:50944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0100840	ORPHA:50944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0000320	ORPHA:50944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0002671	ORPHA:50944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0002860	ORPHA:50944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50944	Schöpf-Schulz-Passarge syndrome		HP:0100615	ORPHA:50944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000272	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000343	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000347	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000369	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000463	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000506	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000518	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000520	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000695	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000773	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000774	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000916	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0000926	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0001538	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0001561	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0001622	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0001680	ORPHA:50945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0001789	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0002089	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0003015	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0003021	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0003027	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0003196	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0005280	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0005616	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0005716	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0005930	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0006402	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0006487	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0006660	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0008905	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0008921	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0010049	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0010306	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0010808	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0011001	ORPHA:50945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50945	Blomstrand lethal chondrodysplasia		HP:0100240	ORPHA:50945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0000639	ORPHA:363429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0000657	ORPHA:363429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0002073	ORPHA:363429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0007256	ORPHA:363429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0000508	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0000543	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0000565	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0000571	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0000666	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001256	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001263	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001290	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001310	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001510	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001583	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001763	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0002075	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0002119	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0002136	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001288	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0002464	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0004322	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0007221	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0007240	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0100275	ORPHA:363429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0001347	ORPHA:363429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0002465	ORPHA:363429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0002828	ORPHA:363429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0003487	ORPHA:363429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0006951	ORPHA:363429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome		HP:0010864	ORPHA:363429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363429	Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome	NOT	HP:0001250	ORPHA:363429	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0000238	ORPHA:251912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0002017	ORPHA:251912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0002315	ORPHA:251912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0002354	ORPHA:251912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0002516	ORPHA:251912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0000492	ORPHA:251912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0000639	ORPHA:251912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0002131	ORPHA:251912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0002922	ORPHA:251912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0030531	ORPHA:251912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0100543	ORPHA:251912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0000364	ORPHA:251912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251912	Pineocytoma		HP:0001288	ORPHA:251912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002086	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002091	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002094	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002207	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002792	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002875	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0003546	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0006530	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0030874	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0031246	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0031631	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0031944	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0031998	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0032341	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0045051	ORPHA:2302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0000961	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0001648	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0001708	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002206	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0002878	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0012418	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0025179	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0030828	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0030849	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0030879	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0031352	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0032016	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0100749	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0100759	ORPHA:2302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0000969	ORPHA:2302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0001685	ORPHA:2302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0030078	ORPHA:2302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0100001	ORPHA:2302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0100721	ORPHA:2302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2302	Asbestos intoxication		HP:0100750	ORPHA:2302	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2301	Congenital short bowel syndrome		HP:0005245	ORPHA:2301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2301	Congenital short bowel syndrome		HP:0002566	ORPHA:2301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2301	Congenital short bowel syndrome		HP:0004322	ORPHA:2301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2301	Congenital short bowel syndrome		HP:0008070	ORPHA:2301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2301	Congenital short bowel syndrome		HP:0100543	ORPHA:2301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2301	Congenital short bowel syndrome		HP:0100578	ORPHA:2301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2301	Congenital short bowel syndrome		HP:0100627	ORPHA:2301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2300	Isolated multiple intestinal atresia		HP:0001561	ORPHA:2300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2300	Isolated multiple intestinal atresia		HP:0100867	ORPHA:2300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2300	Isolated multiple intestinal atresia		HP:0002589	ORPHA:2300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0000982	ORPHA:2309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0007446	ORPHA:2309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0008401	ORPHA:2309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0008404	ORPHA:2309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0012514	ORPHA:2309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0030268	ORPHA:2309	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0002745	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0007410	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0007490	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0007502	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0010765	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0012035	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0025245	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0040036	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0100798	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0200040	ORPHA:2309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0000695	ORPHA:2309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0001508	ORPHA:2309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0001818	ORPHA:2309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0006288	ORPHA:2309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0011968	ORPHA:2309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0025248	ORPHA:2309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0030766	ORPHA:2309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0001596	ORPHA:2309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0001609	ORPHA:2309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0002098	ORPHA:2309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2309	Pachyonychia congenita		HP:0030318	ORPHA:2309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000003	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000023	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000028	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000126	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000174	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000243	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000256	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000286	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000316	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000319	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000324	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000343	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000348	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000358	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000431	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000463	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000465	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000470	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000482	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000486	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000494	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000508	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000518	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000612	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000625	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000656	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000921	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0000964	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001161	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001249	ORPHA:2308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001250	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001263	ORPHA:2308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001274	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001302	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001510	ORPHA:2308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001511	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001522	ORPHA:2308	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001622	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001629	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001650	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001680	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001734	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001763	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001770	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001831	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001847	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001863	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001873	ORPHA:2308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0001883	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002007	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002019	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002021	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002059	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002119	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002205	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002247	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002414	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002566	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002650	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0002827	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0003196	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0003312	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0004322	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0004378	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0004383	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0004397	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0005528	ORPHA:2308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0006101	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0007018	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0007302	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0008872	ORPHA:2308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0009906	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0010059	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0010761	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0100753	ORPHA:2308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2308	Jacobsen syndrome		HP:0100840	ORPHA:2308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0000365	ORPHA:2307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0000486	ORPHA:2307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0001387	ORPHA:2307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0002984	ORPHA:2307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0003510	ORPHA:2307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0001199	ORPHA:2307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0002650	ORPHA:2307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0002974	ORPHA:2307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0005048	ORPHA:2307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0007477	ORPHA:2307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0009778	ORPHA:2307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0000143	ORPHA:2307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0001177	ORPHA:2307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0001873	ORPHA:2307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0001974	ORPHA:2307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0002023	ORPHA:2307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0006660	ORPHA:2307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2307	IVIC syndrome		HP:0011675	ORPHA:2307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0008551	ORPHA:2306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000023	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000175	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000238	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000252	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000347	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000384	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000413	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000463	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000582	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0000932	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0001511	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0001643	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0001647	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0001650	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0001710	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0001713	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0002020	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0005120	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0005301	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0008619	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0008774	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0008897	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0011342	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0011718	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0011968	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0012303	ORPHA:2306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome		HP:0009892	ORPHA:2306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome	NOT	HP:0001888	ORPHA:2306	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2306	Isotretinoin-like syndrome	NOT	HP:0002901	ORPHA:2306	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0000175	ORPHA:2305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0000347	ORPHA:2305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0000356	ORPHA:2305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0000960	ORPHA:2305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0001252	ORPHA:2305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0001315	ORPHA:2305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0001800	ORPHA:2305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0003298	ORPHA:2305	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0004422	ORPHA:2305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0005280	ORPHA:2305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0008551	ORPHA:2305	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2305	Isotretinoin syndrome		HP:0100543	ORPHA:2305	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000200	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000179	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000194	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000218	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000252	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000327	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000348	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000421	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000455	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000490	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000678	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000716	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000718	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000729	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000739	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000750	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0001263	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000817	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000821	ORPHA:293939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0000957	ORPHA:293939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0001249	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0004322	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0001643	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0001655	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0001840	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0002099	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0002829	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0002788	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0003265	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0003324	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0003550	ORPHA:293939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0007018	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0008551	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0010862	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0011234	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0011730	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0012169	ORPHA:293939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0012172	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0030051	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0030084	ORPHA:293939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0012724	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0100710	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293939	Distal Xq28 microduplication syndrome		HP:0100840	ORPHA:293939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70592	Transient predisposition to invasive pyogenic bacterial infection		HP:0001875	ORPHA:70592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70592	Transient predisposition to invasive pyogenic bacterial infection		HP:0002718	ORPHA:70592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70592	Transient predisposition to invasive pyogenic bacterial infection		HP:0002721	ORPHA:70592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70592	Transient predisposition to invasive pyogenic bacterial infection		HP:0005366	ORPHA:70592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70592	Transient predisposition to invasive pyogenic bacterial infection		HP:0007499	ORPHA:70592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70592	Transient predisposition to invasive pyogenic bacterial infection		HP:0005406	ORPHA:70592	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70592	Transient predisposition to invasive pyogenic bacterial infection		HP:0001945	ORPHA:70592	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0002848	ORPHA:70593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0410299	ORPHA:70593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0410300	ORPHA:70593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0410302	ORPHA:70593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0410303	ORPHA:70593	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0000246	ORPHA:70593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0000388	ORPHA:70593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0012384	ORPHA:70593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0030374	ORPHA:70593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0031949	ORPHA:70593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0200117	ORPHA:70593	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0001047	ORPHA:70593	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0002099	ORPHA:70593	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0007274	ORPHA:70593	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency		HP:0010976	ORPHA:70593	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency	NOT	HP:0410240	ORPHA:70593	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency	NOT	HP:0410242	ORPHA:70593	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency	NOT	HP:0410243	ORPHA:70593	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:70593	Immunodeficiency due to selective anti-polysaccharide antibody deficiency	NOT	HP:0410295	ORPHA:70593	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0000225	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0000421	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0000978	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0001107	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0001249	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0001276	ORPHA:352723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0001928	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0002071	ORPHA:352723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0002205	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0002311	ORPHA:352723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0002721	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0007513	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0009830	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0100022	ORPHA:352723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352723	Attenuated Chédiak-Higashi syndrome		HP:0200042	ORPHA:352723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0000338	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0000366	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0000508	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0000708	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0000750	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0000975	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001249	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001270	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001324	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001332	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001337	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001347	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0002063	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0002067	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0002329	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0002360	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0002509	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0005968	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0008936	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0010553	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0100543	ORPHA:70594	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0000252	ORPHA:70594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001250	ORPHA:70594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001510	ORPHA:70594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0001518	ORPHA:70594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70594	Dopa-responsive dystonia due to sepiapterin reductase deficiency		HP:0100021	ORPHA:70594	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0000508	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0000597	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0000639	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0001260	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0001265	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0001336	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0001751	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0002066	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0002151	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0002403	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0002495	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0003200	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0003434	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0003557	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0003701	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0006858	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0007344	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0008619	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0012696	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0025331	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0031422	ORPHA:70595	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0000518	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0000716	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0001250	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0001284	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0001644	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0002076	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0002354	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0002578	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0004389	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70595	Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome		HP:0100543	ORPHA:70595	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000639	ORPHA:280633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001250	ORPHA:280633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001263	ORPHA:280633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0006829	ORPHA:280633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0011344	ORPHA:280633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000218	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000280	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000486	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001156	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001182	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001265	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001337	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001615	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001655	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001773	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002020	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0004488	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0008872	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0010291	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0011247	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0012448	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0200055	ORPHA:280633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000034	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000072	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000126	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000154	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000160	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000212	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000219	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000269	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000286	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000293	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000308	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000316	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000319	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000350	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000396	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000463	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000470	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000498	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000565	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000582	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000646	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000664	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000774	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0000932	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001272	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001347	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001631	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001643	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001667	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001761	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0001804	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002015	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002023	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002025	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002079	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002092	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002100	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002119	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002265	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002286	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002305	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002616	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0002951	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0003196	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0003324	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0004681	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0004742	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0004969	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0005830	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0006165	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0006254	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0007441	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0008551	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0008635	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0008676	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0008718	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0008994	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0010282	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0010544	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0010804	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0010880	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0011271	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0011333	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280633	Multiple congenital anomalies-hypotonia-seizures syndrome		HP:0025025	ORPHA:280633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0000544	ORPHA:98919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0001284	ORPHA:98919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0034122	ORPHA:98919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0000651	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0000666	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0001251	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0002922	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0003457	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0007942	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0010845	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0011499	ORPHA:98919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0000613	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0000622	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0001283	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0001945	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0002273	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0002315	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0003401	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0004372	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0009916	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0010628	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0011347	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0012229	ORPHA:98919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0000508	ORPHA:98919	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0002013	ORPHA:98919	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98919	Miller Fisher syndrome		HP:0002015	ORPHA:98919	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000467	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000508	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002015	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002033	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002882	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003473	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003701	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0004661	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0004889	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0011968	ORPHA:98914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000602	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000961	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001249	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001251	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001283	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001558	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001611	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002205	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001288	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002804	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002872	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003324	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003388	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0004885	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0008443	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0010536	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0011469	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0030842	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0100285	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0100295	ORPHA:98914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000218	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000276	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001250	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001252	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001270	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001284	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001612	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001618	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001761	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002421	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002515	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002751	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003306	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003325	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003458	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0003693	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0009053	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0010307	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0012801	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0030051	ORPHA:98914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000308	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000369	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000407	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000565	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000639	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000651	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0000768	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001265	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001374	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001382	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0001561	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002020	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002392	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0002870	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0005943	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0007178	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes		HP:0025401	ORPHA:98914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98914	Presynaptic congenital myasthenic syndromes	NOT	HP:0030208	ORPHA:98914	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003324	ORPHA:98915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003403	ORPHA:98915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003701	ORPHA:98915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0000467	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0000508	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0000597	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001252	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001263	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001265	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001488	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001612	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002015	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002033	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002093	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002098	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002421	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002460	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002515	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003198	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003398	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003436	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003443	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003691	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0010628	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0012379	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0030203	ORPHA:98915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0000218	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001249	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001284	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001324	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002643	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002650	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002783	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002791	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002815	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003202	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003327	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003388	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003803	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0005216	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0007941	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0010535	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0030211	ORPHA:98915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0000207	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0000303	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001667	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001762	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0001999	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002092	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002359	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0002875	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0003554	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0006251	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98915	Synaptic congenital myasthenic syndromes		HP:0030237	ORPHA:98915	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0007131	ORPHA:98916	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0001265	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0001290	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0001954	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0002307	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0002317	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0003445	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0005335	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0009053	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0012534	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0031162	ORPHA:98916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy		HP:0003383	ORPHA:98916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98916	Acute inflammatory demyelinating polyradiculoneuropathy	NOT	HP:0002066	ORPHA:98916	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003547	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003701	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003749	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0009063	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0009830	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0030226	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0001260	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0001265	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0001288	ORPHA:98911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0001611	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002460	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002540	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002828	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003236	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003458	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003551	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003552	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003557	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003693	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003698	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0003736	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0005085	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0006376	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0006794	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0009027	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0012515	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0012548	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0100297	ORPHA:98911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0000297	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0001638	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002015	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002093	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002792	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002795	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0002878	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0009073	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98911	Distal myotilinopathy		HP:0012496	ORPHA:98911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0008954	ORPHA:98912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0009073	ORPHA:98912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0030198	ORPHA:98912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0001626	ORPHA:98912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0008969	ORPHA:98912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0009005	ORPHA:98912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0009077	ORPHA:98912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0031189	ORPHA:98912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0031374	ORPHA:98912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0001288	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0001638	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0003324	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0003325	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0005162	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0008997	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0009027	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0009072	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0009830	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0011808	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type		HP:0012722	ORPHA:98912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98912	Late-onset distal myopathy, Markesbery-Griggs type	NOT	HP:0002505	ORPHA:98912	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0001324	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0000218	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0000496	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0000508	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0000597	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0001315	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0001446	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003202	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003388	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003402	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003403	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003443	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003458	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003484	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003547	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003722	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0003803	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0009005	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0010628	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0030199	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0410011	ORPHA:98913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0000651	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0000961	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0002091	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0002194	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0002329	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0002650	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0002792	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0002875	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0002878	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0005659	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0009077	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0012515	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0012764	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0030196	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0031108	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98913	Postsynaptic congenital myasthenic syndromes		HP:0031374	ORPHA:98913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000179	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000252	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000294	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000341	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000358	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000463	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000486	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000527	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0000574	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0001007	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0001263	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0001274	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0001276	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0001320	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0001344	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0001510	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0002470	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0002509	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0002553	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0010864	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0011451	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0100540	ORPHA:466688	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		HP:0002465	ORPHA:466688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0012240	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0012472	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0040081	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001413	ORPHA:98907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0007009	ORPHA:98907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis	NOT	HP:0001513	ORPHA:98907	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis	NOT	HP:0001946	ORPHA:98907	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0007479	ORPHA:98907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0009073	ORPHA:98907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0000385	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0000407	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0000486	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0000508	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0000523	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0000639	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0000656	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001251	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001263	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001284	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001397	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001596	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001638	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001911	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0002155	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0002240	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0001288	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0002910	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0002922	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0003198	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0003458	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0003547	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98907	Neutral lipid storage disease with ichthyosis		HP:0004322	ORPHA:98907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0003547	ORPHA:98908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0009073	ORPHA:98908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0012240	ORPHA:98908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0012548	ORPHA:98908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001270	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001290	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001397	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001638	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0002155	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001288	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0002380	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0002910	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0003198	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0003326	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0003388	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0003391	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0003749	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0008167	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0009046	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0025435	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0040081	ORPHA:98908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0000407	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0000467	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0000819	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001256	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001284	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001635	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0002240	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0003805	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0004322	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0006280	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0009027	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0009055	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0009063	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0030237	ORPHA:98908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0001082	ORPHA:98908	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy		HP:0012683	ORPHA:98908	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy	NOT	HP:0001513	ORPHA:98908	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98908	Neutral lipid storage disease with myopathy	NOT	HP:0008064	ORPHA:98908	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0003323	ORPHA:98909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0003327	ORPHA:98909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0009053	ORPHA:98909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0001635	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0001678	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0001288	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0002505	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0002747	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0005115	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0005157	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0030196	ORPHA:98909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0001645	ORPHA:98909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0002522	ORPHA:98909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0003722	ORPHA:98909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0005659	ORPHA:98909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0030192	ORPHA:98909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0030319	ORPHA:98909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98909	Desminopathy		HP:0003306	ORPHA:98909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0012415	ORPHA:70578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0012418	ORPHA:70578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0011117	ORPHA:70578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0001942	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0002615	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0002878	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0011118	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0030783	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0031273	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0100598	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0100806	ORPHA:70578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0002090	ORPHA:70578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0001733	ORPHA:70578	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0001953	ORPHA:70578	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0002633	ORPHA:70578	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0002094	ORPHA:70578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70578	Adult acute respiratory distress syndrome		HP:0002113	ORPHA:70578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000544	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001270	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001290	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001324	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001558	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0002058	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0002795	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003327	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003557	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003560	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003701	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003803	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0009025	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0010628	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0011805	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0011807	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0011968	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0031237	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0100293	ORPHA:98905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000028	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000046	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000054	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000218	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000275	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000508	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0000969	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001349	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001371	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001382	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0001561	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0002090	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0002205	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0002650	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0002878	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003202	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003547	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0003798	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0008850	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0009046	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0010804	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0011399	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0012036	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0031139	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98905	Congenital multicore myopathy with external ophthalmoplegia		HP:0040191	ORPHA:98905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0001528	ORPHA:293964	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0000771	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0001325	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0001520	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0001956	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0001958	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0001985	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0001998	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0002173	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0006568	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0030812	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy		HP:0040214	ORPHA:293964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy	NOT	HP:0002960	ORPHA:293964	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:293964	Hypoinsulinemic hypoglycemia and body hemihypertrophy	NOT	HP:0030781	ORPHA:293964	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0011505	ORPHA:411527	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0030497	ORPHA:411527	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0031805	ORPHA:411527	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0000572	ORPHA:411527	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0001085	ORPHA:411527	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0012841	ORPHA:411527	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0040049	ORPHA:411527	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0000501	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0000580	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0000608	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0000622	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0001129	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0004328	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0007984	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0030666	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411527	Central retinal vein occlusion		HP:0100014	ORPHA:411527	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000130	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000160	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000238	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000256	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000271	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000308	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000316	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000358	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000463	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000478	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0000504	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0001249	ORPHA:59315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0001251	ORPHA:59315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0001626	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0002023	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0002032	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0002119	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0002251	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0002335	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0002575	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0003196	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0006101	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0006899	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0009803	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0009943	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0010442	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0010664	ORPHA:59315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0012210	ORPHA:59315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0100321	ORPHA:59315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:59315	Rhombencephalosynapsis		HP:0100842	ORPHA:59315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0000768	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0001270	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0001319	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0001337	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0003044	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0003273	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0003323	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0003458	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0003803	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0007126	ORPHA:98902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy		HP:0002747	ORPHA:98902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:98902	Amish nemaline myopathy	NOT	HP:0001249	ORPHA:98902	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0001004	ORPHA:90186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0000987	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0001581	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0002732	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0002849	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0003550	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0005406	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0010741	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0010781	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0031288	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0100658	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0200041	ORPHA:90186	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0000282	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0002202	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0002619	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0007514	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0012027	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0012398	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0100539	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0200042	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90186	Meige disease		HP:0200058	ORPHA:90186	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0002027	ORPHA:466677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0012547	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0031416	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0004360	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001919	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001735	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0011675	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001251	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0000622	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0011710	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0031546	ORPHA:466677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0030149	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0025143	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001635	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0002014	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001260	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0100660	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0000969	ORPHA:466677	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0031956	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0010783	ORPHA:466677	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0003781	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001945	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0003076	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0010828	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0003074	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0000975	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0002487	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001347	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0000822	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0002900	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0031185	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0032232	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0025435	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0410173	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0002919	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0000616	ORPHA:466677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0005967	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0011499	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0012819	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001336	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0012531	ORPHA:466677	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0003401	ORPHA:466677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0200023	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0025072	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0100598	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0000979	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001950	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0000711	ORPHA:466677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0003201	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0012250	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001250	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001297	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0010872	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001649	ORPHA:466677	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0002789	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0001337	ORPHA:466677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0006682	ORPHA:466677	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466677	Scorpion envenomation		HP:0002013	ORPHA:466677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86918	Diffuse palmoplantar keratoderma-acrocyanosis syndrome		HP:0001063	ORPHA:86918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86918	Diffuse palmoplantar keratoderma-acrocyanosis syndrome		HP:0007447	ORPHA:86918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86919	Keratosis palmaris et plantaris-clinodactyly syndrome		HP:0000975	ORPHA:86919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86919	Keratosis palmaris et plantaris-clinodactyly syndrome		HP:0004209	ORPHA:86919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:86919	Keratosis palmaris et plantaris-clinodactyly syndrome		HP:0007447	ORPHA:86919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0001635	ORPHA:70591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002092	ORPHA:70591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0005317	ORPHA:70591	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0001962	ORPHA:70591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002204	ORPHA:70591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002625	ORPHA:70591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002792	ORPHA:70591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002875	ORPHA:70591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0012378	ORPHA:70591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0030877	ORPHA:70591	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0000716	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0000969	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0001279	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0001513	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0001693	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0001708	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0001871	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002960	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0003613	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0004831	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0005133	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0005135	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0005162	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0010536	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0011227	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0011712	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0011901	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0012146	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0012184	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0012417	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0025343	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0030718	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0030977	ORPHA:70591	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002037	ORPHA:70591	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002664	ORPHA:70591	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0002754	ORPHA:70591	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70591	Chronic thromboembolic pulmonary hypertension		HP:0005547	ORPHA:70591	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000256	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000733	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000739	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000750	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0001249	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0001963	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0002007	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0031936	ORPHA:397612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000218	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000303	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000308	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000431	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000494	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0000729	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0001250	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0001252	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0001363	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0001433	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0004209	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0006532	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0010845	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0011220	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0030799	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0045025	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0100540	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397612	Macrocephaly-developmental delay syndrome		HP:0100716	ORPHA:397612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169095	Severe combined immunodeficiency due to FOXN1 deficiency		HP:0001803	ORPHA:169095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169095	Severe combined immunodeficiency due to FOXN1 deficiency		HP:0001807	ORPHA:169095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169095	Severe combined immunodeficiency due to FOXN1 deficiency		HP:0002721	ORPHA:169095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169095	Severe combined immunodeficiency due to FOXN1 deficiency		HP:0005403	ORPHA:169095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169095	Severe combined immunodeficiency due to FOXN1 deficiency		HP:0005597	ORPHA:169095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0000389	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0000705	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0001252	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0001287	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0001945	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002090	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002718	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002721	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002841	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002960	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0003198	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0004429	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0007676	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0011084	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0011274	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0100806	ORPHA:169090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0000970	ORPHA:169090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0001744	ORPHA:169090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002240	ORPHA:169090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002716	ORPHA:169090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0001873	ORPHA:169090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0001878	ORPHA:169090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169090	Combined immunodeficiency due to CRAC channel dysfunction		HP:0002664	ORPHA:169090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000154	ORPHA:293948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000256	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000293	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000347	ORPHA:293948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000455	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000483	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000490	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000504	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000545	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000582	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000708	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000718	ORPHA:293948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000729	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000742	ORPHA:293948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0000750	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0001249	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0001256	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0001263	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0001382	ORPHA:293948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0001513	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0003196	ORPHA:293948	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0100716	ORPHA:293948	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0100738	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0100962	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293948	1p21.3 microdeletion syndrome		HP:0400004	ORPHA:293948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0001698	ORPHA:48686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0002027	ORPHA:48686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0002094	ORPHA:48686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0002202	ORPHA:48686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0002585	ORPHA:48686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0002721	ORPHA:48686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0003270	ORPHA:48686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48686	Primary effusion lymphoma		HP:0012191	ORPHA:48686	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000670	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000679	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000682	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000691	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000958	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000962	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0001092	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0001171	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0001803	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0001839	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0002208	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0008404	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0009804	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0045075	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0100257	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000068	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000126	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000574	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000632	ORPHA:1896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000202	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000491	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000498	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000613	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000620	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000968	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0001096	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0002217	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0004275	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0007513	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0008065	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0008678	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0012165	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0100533	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0200020	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0410030	ORPHA:1896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000047	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000076	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000175	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000217	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000359	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000370	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000407	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000453	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000621	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000778	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000824	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000830	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000966	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0001249	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0001770	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0002213	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0002665	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0003764	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0004322	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0006101	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0006709	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0008070	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0000377	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0009601	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0009623	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1896	EEC syndrome		HP:0010311	ORPHA:1896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000160	ORPHA:1895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000233	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000238	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000347	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000369	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000453	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000463	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0000664	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001007	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001088	ORPHA:1895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001238	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001249	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001250	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001276	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001387	ORPHA:1895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001508	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0001608	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0002007	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0002093	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0002162	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0002230	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0002269	ORPHA:1895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0002714	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0003196	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0005616	ORPHA:1895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0008056	ORPHA:1895	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0009465	ORPHA:1895	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1895	Edinburgh malformation syndrome		HP:0100807	ORPHA:1895	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1892	Ectrodactyly-polydactyly syndrome		HP:0001162	ORPHA:1892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1892	Ectrodactyly-polydactyly syndrome		HP:0100257	ORPHA:1892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1892	Ectrodactyly-polydactyly syndrome		HP:0001156	ORPHA:1892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1892	Ectrodactyly-polydactyly syndrome		HP:0005916	ORPHA:1892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1892	Ectrodactyly-polydactyly syndrome		HP:0006101	ORPHA:1892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1892	Ectrodactyly-polydactyly syndrome		HP:0009773	ORPHA:1892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1892	Ectrodactyly-polydactyly syndrome		HP:0100490	ORPHA:1892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0001518	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0001622	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002088	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002094	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002097	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002098	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0004887	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0006528	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0012419	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0012735	ORPHA:70589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0001607	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0001667	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0001708	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002360	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002780	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002795	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002871	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0003546	ORPHA:70589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0004890	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0006536	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0006597	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0012252	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0030828	ORPHA:70589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0002786	ORPHA:70589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0030878	ORPHA:70589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0100632	ORPHA:70589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70589	Bronchopulmonary dysplasia		HP:0100750	ORPHA:70589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0001249	ORPHA:1891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0001257	ORPHA:1891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0001258	ORPHA:1891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0001347	ORPHA:1891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0002817	ORPHA:1891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0003272	ORPHA:1891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0004209	ORPHA:1891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0006101	ORPHA:1891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1891	Intellectual disability-spasticity-ectrodactyly syndrome		HP:0007598	ORPHA:1891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0000154	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0000687	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0001010	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0001250	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0001256	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0001513	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002353	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002395	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0004485	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0005484	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0005599	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0007730	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0008947	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0040082	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0040196	ORPHA:411511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0000303	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0000486	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0000748	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0001251	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0001263	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002015	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002033	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002046	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002136	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002141	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002167	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0002307	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0005469	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0010808	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0011968	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0100022	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0100023	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0100703	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411511	Angelman syndrome due to a point mutation		HP:0100738	ORPHA:411511	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0001905	ORPHA:182050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0000083	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0000093	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0000112	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0000123	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0000132	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0000407	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0000978	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0001902	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0002910	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0003010	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0004406	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0007819	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0008264	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0011877	ORPHA:182050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:182050	MYH9-related syndromic thrombocytopenia		HP:0001658	ORPHA:182050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0000748	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0001010	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0001250	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0001513	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0001999	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0002353	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0002591	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0005599	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0007730	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0008872	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0008947	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0031936	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0040082	ORPHA:411515	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0000154	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0000303	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0000708	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0000710	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0000736	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0000752	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0001251	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0001344	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0002136	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0002307	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0002465	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0004485	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0006979	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411515	Angelman syndrome due to imprinting defect in 15q11-q13		HP:0410263	ORPHA:411515	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0002098	ORPHA:70588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0005828	ORPHA:70588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0011410	ORPHA:70588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0025116	ORPHA:70588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0031169	ORPHA:70588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0031860	ORPHA:70588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0031983	ORPHA:70588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0001511	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0001788	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0002092	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0002107	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0008071	ORPHA:70588	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0009800	ORPHA:70588	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0011951	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0012418	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0012420	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0012768	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0025421	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0030828	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0100750	ORPHA:70588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0001298	ORPHA:70588	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:70588	Meconium aspiration syndrome		HP:0010444	ORPHA:70588	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0000963	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0000974	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0001001	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0001252	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0001373	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0001385	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0001387	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0002300	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0002381	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0002673	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0002812	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0002827	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0003510	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0001382	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0005743	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0010529	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0010547	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0100699	ORPHA:1899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0000278	ORPHA:1899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0000286	ORPHA:1899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0000316	ORPHA:1899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0000347	ORPHA:1899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0002650	ORPHA:1899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0005280	ORPHA:1899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0000023	ORPHA:1899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1899	Arthrochalasia Ehlers-Danlos syndrome		HP:0100541	ORPHA:1899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0000613	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0000635	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0000639	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0000649	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0000992	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0007513	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0007663	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0007680	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0007730	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0007750	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0011358	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0012805	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0025551	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0025568	ORPHA:352731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0000486	ORPHA:352731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0000646	ORPHA:352731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0002226	ORPHA:352731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0002227	ORPHA:352731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0001072	ORPHA:352731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0008069	ORPHA:352731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:352731	Oculocutaneous albinism type 1		HP:0025127	ORPHA:352731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0000486	ORPHA:1897	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0000488	ORPHA:1897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0000504	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0000670	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0000687	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0001592	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0002223	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0002231	ORPHA:1897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0006101	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0006482	ORPHA:1897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0007703	ORPHA:1897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0007754	ORPHA:1897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0100257	ORPHA:1897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0000478	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0000691	ORPHA:1897	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1897	EEM syndrome		HP:0002209	ORPHA:1897	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0007020	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0000252	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0008848	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0001256	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0008376	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0002194	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0002191	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0002395	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0011448	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0003487	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0000175	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0000193	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0030625	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0007814	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0007199	ORPHA:506353	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0004302	ORPHA:506353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0030182	ORPHA:506353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0007220	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0001250	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0007768	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0007663	ORPHA:506353	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506353	Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction		HP:0002493	ORPHA:506353	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000179	ORPHA:506358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000272	ORPHA:506358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000337	ORPHA:506358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000414	ORPHA:506358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001263	ORPHA:506358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001999	ORPHA:506358	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000307	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000324	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000358	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000486	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000494	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000629	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000708	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000750	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001252	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001256	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001511	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002342	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0008872	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0011339	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0011471	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0031936	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0200136	ORPHA:506358	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000028	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000074	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000126	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000164	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000218	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000268	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000297	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000347	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000369	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000483	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000506	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000508	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000540	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000717	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000729	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000739	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000821	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000824	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0000974	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001274	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001332	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001337	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001344	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001363	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001518	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001655	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001822	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0001852	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002032	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002079	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002119	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002171	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002236	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002500	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002515	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0002719	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0003006	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0003187	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0005684	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0006094	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0007018	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0007678	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0008944	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0010316	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0010499	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0010864	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0011311	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0011344	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0012448	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506358	Gabriele-de Vries syndrome		HP:0045075	ORPHA:506358	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0000403	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0001325	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0001988	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0002615	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0002788	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0002837	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0002902	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0002920	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0004313	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0004429	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0010976	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0006532	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0008163	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0011108	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0011735	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0012378	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0100776	ORPHA:293978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0001596	ORPHA:293978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0002110	ORPHA:293978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0004332	ORPHA:293978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0008404	ORPHA:293978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0012504	ORPHA:293978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0100803	ORPHA:293978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0000651	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0000824	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0001263	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0001508	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0001973	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0002121	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0003765	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0007418	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0030349	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0030353	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome		HP:0100806	ORPHA:293978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome	NOT	HP:0001045	ORPHA:293978	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome	NOT	HP:0002153	ORPHA:293978	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome	NOT	HP:0030057	ORPHA:293978	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:293978	Deficiency in anterior pituitary function-variable immunodeficiency syndrome	NOT	HP:0100646	ORPHA:293978	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0004313	ORPHA:436159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0001047	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0001744	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0001890	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0001973	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002014	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002090	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002240	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002716	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002720	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002783	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002788	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002850	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0004315	ORPHA:436159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0000964	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0001510	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0001904	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002037	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002110	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002582	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002665	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0003765	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0005401	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0032216	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0100280	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0100646	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0100651	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0100806	ORPHA:436159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0002069	ORPHA:436159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0012410	ORPHA:436159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436159	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency		HP:0100653	ORPHA:436159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000122	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000482	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000543	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002135	ORPHA:90324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002446	ORPHA:90324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002461	ORPHA:90324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0007346	ORPHA:90324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0012447	ORPHA:90324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000011	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000992	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001256	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001284	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001347	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002080	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002317	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001288	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0003134	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0003202	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0003477	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0004302	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0004934	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0005181	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0007108	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0008615	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0009830	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0012444	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0012762	ORPHA:90324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000016	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000072	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000083	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000126	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000253	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000331	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000400	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000405	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000460	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000486	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000490	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000518	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000540	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000613	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000639	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000670	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001250	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001530	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001999	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002020	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002216	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002240	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002344	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002650	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002808	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002910	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0006297	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0011359	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0011968	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0012758	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0032263	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0100543	ORPHA:90324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000089	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000546	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000556	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000568	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0000573	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001097	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001105	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001297	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001371	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001638	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0001744	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0002616	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0011527	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0012804	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90324	Cockayne syndrome type 3		HP:0100309	ORPHA:90324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000256	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000316	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000407	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000463	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000633	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000729	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0012760	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000824	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000864	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000961	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000966	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0001513	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002342	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002418	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002591	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002791	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002902	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002910	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0003074	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0003077	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0005280	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0007110	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0008213	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0011220	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0011787	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0011968	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0012332	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0012412	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0012704	ORPHA:293987	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000232	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000718	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000863	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000870	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0001263	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0001945	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0001959	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002045	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002099	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002376	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002579	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002650	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002783	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002788	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002870	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0003005	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0004322	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0005616	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0006747	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0007328	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0007695	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0011748	ORPHA:293987	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000709	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000712	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000716	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000722	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000805	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0000823	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0001156	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0001250	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0001290	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002383	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0002608	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0006543	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0030050	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome		HP:0100716	ORPHA:293987	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome	NOT	HP:0000739	ORPHA:293987	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:293987	Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome	NOT	HP:0002153	ORPHA:293987	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000276	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000303	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000505	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000518	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000633	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000648	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000822	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000966	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001251	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001288	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001337	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001347	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002014	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002172	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001288	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002650	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0003134	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0003138	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0004370	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0005328	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000083	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000331	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000400	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000486	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000509	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000528	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000554	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000613	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000639	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000674	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000680	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001034	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001250	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001252	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001903	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002061	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002240	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002360	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0006297	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0006313	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0006334	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0100699	ORPHA:90321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000026	ORPHA:90321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000028	ORPHA:90321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000365	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000490	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000580	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000992	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001249	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001508	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0001999	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002135	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0002910	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0004463	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0008366	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0008897	ORPHA:90321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000093	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90321	Cockayne syndrome type 1		HP:0000164	ORPHA:90321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001249	ORPHA:90322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001511	ORPHA:90322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001999	ORPHA:90322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0002545	ORPHA:90322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0007346	ORPHA:90322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0012758	ORPHA:90322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000276	ORPHA:90322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000303	ORPHA:90322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001251	ORPHA:90322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001288	ORPHA:90322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0002172	ORPHA:90322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001288	ORPHA:90322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0005328	ORPHA:90322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000331	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000365	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000400	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000486	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000505	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000509	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000519	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000528	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000554	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000613	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000639	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000674	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000680	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001034	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0001371	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0002061	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0002240	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0002509	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0002650	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0002808	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0006297	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0006313	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0006334	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0008872	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0008936	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0100699	ORPHA:90322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000026	ORPHA:90322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90322	Cockayne syndrome type 2		HP:0000028	ORPHA:90322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0001945	ORPHA:454836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0003326	ORPHA:454836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0012378	ORPHA:454836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0012735	ORPHA:454836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0025439	ORPHA:454836	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0001873	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0001882	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0001888	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002113	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002315	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0011227	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0012418	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0025179	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0031246	ORPHA:454836	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0000509	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002013	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002014	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002027	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002090	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002094	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002202	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002878	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0005268	ORPHA:454836	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0025435	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0031245	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0100749	ORPHA:454836	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0001287	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0001635	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0001919	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002098	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002107	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002383	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002789	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0002910	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0003073	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0003201	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0003236	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0005521	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0012115	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0012486	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454836	Avian influenza		HP:0100806	ORPHA:454836	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001954	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002019	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002046	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002079	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002263	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002558	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002572	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002578	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002579	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002705	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002877	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0003186	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0003388	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0003422	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0004389	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0004442	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0004443	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0004467	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0004942	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0005487	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0006481	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0007328	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0007655	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0008872	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0009794	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0009804	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0010297	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0010807	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0011147	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0011330	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0011470	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0011807	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0100259	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000637	ORPHA:453504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001252	ORPHA:453504	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000028	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000076	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000126	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000158	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000194	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000252	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000276	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000431	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000455	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000689	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001363	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001385	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001510	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001627	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001629	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002282	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002342	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002465	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002540	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002650	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002711	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0002714	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0003763	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0010864	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0010880	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0031936	ORPHA:453504	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000175	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000193	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000280	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000405	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000407	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000411	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000430	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000476	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000508	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000540	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000545	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000586	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000587	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000589	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000609	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000821	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000938	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0000975	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001250	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001274	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001284	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001315	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001324	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001382	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001548	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001631	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001647	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001762	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453504	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation		HP:0001763	ORPHA:453504	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0000980	ORPHA:56425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0001324	ORPHA:56425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0001744	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0001878	ORPHA:56425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0002014	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0002017	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0002240	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0002315	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0002716	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0002829	ORPHA:56425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0002960	ORPHA:56425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0003418	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0012086	ORPHA:56425	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:56425	Cold agglutinin disease		HP:0012378	ORPHA:56425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000657	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001290	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001321	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001508	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002007	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002119	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002419	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002789	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0004719	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0011933	ORPHA:397715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000047	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000083	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000110	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000286	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000316	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000347	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000358	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000369	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000396	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000545	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000556	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000572	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000773	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000803	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0000890	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001156	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001263	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001273	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001305	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001317	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001320	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001331	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001344	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0001591	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002020	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002085	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002100	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002104	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002134	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002195	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002205	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002280	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002435	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002516	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002558	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0002910	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0003170	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0003411	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0004322	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0004629	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0004991	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0005257	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0005280	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0005989	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0006528	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0006610	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0006668	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0006711	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0006956	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0007082	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0008445	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0008797	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0009921	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0010013	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0010579	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0011927	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0011968	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0012106	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0012795	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0030048	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0031528	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0100259	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy		HP:0100954	ORPHA:397715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0033978	ORPHA:309162	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0001251	ORPHA:309162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0001260	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0001272	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0001288	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0001508	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002311	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0003202	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0003701	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0007256	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0100543	ORPHA:309162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0000020	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0001250	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002014	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002015	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002019	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002059	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002071	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002380	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0002460	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0003121	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0031006	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0100785	ORPHA:309162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0000729	ORPHA:309162	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0001761	ORPHA:309162	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309162	Sandhoff disease, juvenile form		HP:0100786	ORPHA:309162	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000028	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000044	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000054	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000193	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000252	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000316	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000347	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000411	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000444	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000545	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001263	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000771	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000786	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000823	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000831	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0000912	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001007	ORPHA:293967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001123	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001250	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001270	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001276	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001328	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0004322	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001562	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001761	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001845	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0001935	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0002061	ORPHA:293967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0002553	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0002750	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0002857	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0010055	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0008527	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0009185	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0003799	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0006353	ORPHA:293967	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0007266	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0007642	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0008734	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0008850	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0011246	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0011304	ORPHA:293967	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0011343	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0011408	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0011968	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0012795	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293967	Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome		HP:0100689	ORPHA:293967	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0033978	ORPHA:309169	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0001257	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0001260	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0001268	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0001337	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0002015	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0002066	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0003390	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0003484	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0008994	ORPHA:309169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0000739	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0001315	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0001332	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0002380	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0003236	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0003394	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0004373	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0025268	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309169	Sandhoff disease, adult form		HP:0100295	ORPHA:309169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0000256	ORPHA:210548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0000729	ORPHA:210548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0000750	ORPHA:210548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001249	ORPHA:210548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001270	ORPHA:210548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0000957	ORPHA:210548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001012	ORPHA:210548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001054	ORPHA:210548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001252	ORPHA:210548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0005280	ORPHA:210548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0031447	ORPHA:210548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0200008	ORPHA:210548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0000316	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001177	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001250	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001397	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0001829	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0002007	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0002890	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0003196	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0006781	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0007018	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0011800	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:210548	Macrocephaly-intellectual disability-autism syndrome		HP:0032203	ORPHA:210548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69744	Circumscribed palmoplantar hypokeratosis		HP:0001227	ORPHA:69744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69744	Circumscribed palmoplantar hypokeratosis		HP:0010486	ORPHA:69744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69744	Circumscribed palmoplantar hypokeratosis		HP:0011121	ORPHA:69744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69744	Circumscribed palmoplantar hypokeratosis		HP:0100872	ORPHA:69744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69744	Circumscribed palmoplantar hypokeratosis		HP:0200035	ORPHA:69744	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0004334	ORPHA:454831	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0000953	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001009	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001010	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001324	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001873	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001888	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001892	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001945	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0002013	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0002014	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0002315	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0040189	ORPHA:454831	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0000518	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0000962	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001250	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0001913	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0002321	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0002615	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0006515	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0007185	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0011123	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0012378	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454831	Acute radiation syndrome		HP:0200042	ORPHA:454831	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1995	Cleft lip-retinopathy syndrome		HP:0000488	ORPHA:1995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1995	Cleft lip-retinopathy syndrome		HP:0000505	ORPHA:1995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1995	Cleft lip-retinopathy syndrome		HP:0007703	ORPHA:1995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1995	Cleft lip-retinopathy syndrome		HP:0100335	ORPHA:1995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0007990	ORPHA:69736	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0008034	ORPHA:69736	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0000593	ORPHA:69736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0000613	ORPHA:69736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0011488	ORPHA:69736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0012372	ORPHA:69736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0200026	ORPHA:69736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0002788	ORPHA:69736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0012631	ORPHA:69736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69736	Bilateral acute depigmentation of the iris		HP:0012634	ORPHA:69736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000161	ORPHA:1993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000175	ORPHA:1993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000190	ORPHA:1993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000193	ORPHA:1993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000316	ORPHA:1993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000494	ORPHA:1993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000506	ORPHA:1993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0000612	ORPHA:1993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0001482	ORPHA:1993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0002084	ORPHA:1993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0004122	ORPHA:1993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0005280	ORPHA:1993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0006866	ORPHA:1993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0007370	ORPHA:1993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0010609	ORPHA:1993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1993	Pai syndrome		HP:0100582	ORPHA:1993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436144	Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome		HP:0001511	ORPHA:436144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436144	Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome		HP:0004322	ORPHA:436144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436144	Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome		HP:0008734	ORPHA:436144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0000561	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0001596	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0002209	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0002223	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0002231	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0003550	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0100763	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0100869	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0100870	ORPHA:69735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0000034	ORPHA:69735	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0000965	ORPHA:69735	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0100540	ORPHA:69735	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0001541	ORPHA:69735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0001789	ORPHA:69735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0002202	ORPHA:69735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69735	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome		HP:0004334	ORPHA:69735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0000280	ORPHA:436141	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0000486	ORPHA:436141	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0001252	ORPHA:436141	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0002857	ORPHA:436141	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0003028	ORPHA:436141	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0006094	ORPHA:436141	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0010864	ORPHA:436141	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0001513	ORPHA:436141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0001250	ORPHA:436141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0001288	ORPHA:436141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436141	HIDEA syndrome		HP:0002360	ORPHA:436141	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0001072	ORPHA:31112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0001482	ORPHA:31112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0008069	ORPHA:31112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0010783	ORPHA:31112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0100244	ORPHA:31112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0200042	ORPHA:31112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0012531	ORPHA:31112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31112	Dermatofibrosarcoma protuberans		HP:0002716	ORPHA:31112	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000280	ORPHA:397709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000750	ORPHA:397709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002194	ORPHA:397709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0007360	ORPHA:397709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0010862	ORPHA:397709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0010864	ORPHA:397709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0011344	ORPHA:397709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000158	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000407	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000639	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000729	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001251	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001252	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001344	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002007	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002136	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002751	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0004482	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0011842	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0100540	ORPHA:397709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000218	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000289	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000293	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000307	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000343	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000350	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000431	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000506	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000678	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0000768	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001156	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001250	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001257	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001265	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001433	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001631	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001643	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0001762	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002002	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002186	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002219	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002500	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0002684	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0003487	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0005280	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0006951	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0008443	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0010471	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0012110	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0012385	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0012471	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0012745	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0012810	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397709	Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome		HP:0030084	ORPHA:397709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0000316	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0000405	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0000478	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0000492	ORPHA:1997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0000504	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0000670	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0000698	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0002023	ORPHA:1997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0100337	ORPHA:1997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0006101	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0007651	ORPHA:1997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0009743	ORPHA:1997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0011362	ORPHA:1997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0012905	ORPHA:1997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1997	Blepharo-cheilo-odontic syndrome		HP:0200040	ORPHA:1997	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0002451	ORPHA:210571	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0000473	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0001260	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0001300	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0001347	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0001618	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0002015	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0002067	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0002174	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0002310	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0002317	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0007256	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0012514	ORPHA:210571	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0001270	ORPHA:210571	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210571	Dystonia 16		HP:0001249	ORPHA:210571	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0033978	ORPHA:309155	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0001250	ORPHA:309155	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0001347	ORPHA:309155	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0002376	ORPHA:309155	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0008936	ORPHA:309155	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0012758	ORPHA:309155	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0001257	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0001336	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0002069	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0002120	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0002267	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0003429	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0004481	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0007083	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0010729	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0012696	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0032794	ORPHA:309155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0000280	ORPHA:309155	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0001433	ORPHA:309155	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0001653	ORPHA:309155	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0010780	ORPHA:309155	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0100814	ORPHA:309155	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309155	Sandhoff disease, infantile form		HP:0001634	ORPHA:309155	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0000105	ORPHA:90301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0000147	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0000831	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0000845	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0000855	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0000956	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0001007	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0003394	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90301	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome		HP:0008675	ORPHA:90301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0002270	ORPHA:43116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000711	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000737	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000739	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001268	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001289	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001336	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001337	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001649	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0002014	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0002018	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0100785	ORPHA:43116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000570	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000713	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000822	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000975	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001250	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001347	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0002169	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0002789	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0003128	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0011499	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0032044	ORPHA:43116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0000738	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001259	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001276	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001399	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001919	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0001945	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0002063	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0002615	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0003201	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0005521	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:43116	Serotonin syndrome		HP:0031258	ORPHA:43116	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0001433	ORPHA:457077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0001873	ORPHA:457077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0002716	ORPHA:457077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0011227	ORPHA:457077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0012050	ORPHA:457077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0000083	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0001541	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0001744	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0001903	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0001945	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0001974	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0002202	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0002240	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0003155	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0005513	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0011974	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0030783	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0031052	ORPHA:457077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome		HP:0025435	ORPHA:457077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome	NOT	HP:0002664	ORPHA:457077	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome	NOT	HP:0002960	ORPHA:457077	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome	NOT	HP:0012156	ORPHA:457077	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome	NOT	HP:0031691	ORPHA:457077	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome	NOT	HP:0032262	ORPHA:457077	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457077	TAFRO syndrome	NOT	HP:0032288	ORPHA:457077	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000298	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000709	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000726	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000739	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000751	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0001250	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0001266	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0001337	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002063	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002067	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002135	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002315	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002321	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002344	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0007146	ORPHA:1980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000012	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000802	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0000822	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0001332	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0001350	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002015	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002312	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002317	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0002354	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0003388	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0100660	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0003394	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0004305	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0007256	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0007352	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis		HP:0031987	ORPHA:1980	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis	NOT	HP:0011450	ORPHA:1980	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1980	Bilateral striopallidodentate calcinosis	NOT	HP:0032180	ORPHA:1980	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000160	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000399	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000407	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000408	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000518	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000574	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000519	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0000824	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0001270	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0002827	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0004322	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0002571	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0002650	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0002652	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0002655	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0002857	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0009830	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0003162	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0003416	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0005659	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0007470	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0008445	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0008619	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436174	Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome		HP:0011220	ORPHA:436174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002814	ORPHA:90307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0100026	ORPHA:90307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0001722	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002617	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002619	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0004947	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0004948	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0007394	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0008968	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0012721	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0025104	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0025474	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0032555	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0100553	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0100784	ORPHA:90307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0000016	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0000079	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0000100	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0001892	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002138	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002196	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002315	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002390	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002408	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002817	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0002936	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0003418	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0003474	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0005521	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0006489	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0007340	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0010484	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0012514	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0012531	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0030833	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0031138	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0031939	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0040189	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0100749	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0100766	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0100775	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0200042	ORPHA:90307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0007461	ORPHA:90307	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90307	Parkes Weber syndrome		HP:0010550	ORPHA:90307	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0000098	ORPHA:90308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0000140	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0000252	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0000256	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0000790	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0000929	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0000969	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001028	ORPHA:90308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001249	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001541	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001631	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001635	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001643	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001702	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001789	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0001935	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0002093	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0002204	ORPHA:90308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0002239	ORPHA:90308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0002240	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0003010	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0004414	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0004936	ORPHA:90308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0005293	ORPHA:90308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0011029	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0011842	ORPHA:90308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0100559	ORPHA:90308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0100560	ORPHA:90308	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0100658	ORPHA:90308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0100724	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90308	Capillary-lymphatic-venous malformation with segmental distribution		HP:0100784	ORPHA:90308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0011834	ORPHA:280679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000027	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000278	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000316	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000343	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000518	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000707	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000815	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000822	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000823	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0001342	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0001644	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0001999	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0002140	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0002216	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0004302	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0004322	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0007970	ORPHA:280679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000369	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000445	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000454	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000490	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0000824	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0001263	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0001324	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0001677	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280679	Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome		HP:0008734	ORPHA:280679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53372	Hereditary geniospasm		HP:0012462	ORPHA:53372	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:53372	Hereditary geniospasm		HP:3000007	ORPHA:53372	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53372	Hereditary geniospasm		HP:0000178	ORPHA:53372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53372	Hereditary geniospasm		HP:0012433	ORPHA:53372	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53372	Hereditary geniospasm	NOT	HP:0002080	ORPHA:53372	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:53372	Hereditary geniospasm	NOT	HP:0002353	ORPHA:53372	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:53372	Hereditary geniospasm	NOT	HP:0003457	ORPHA:53372	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000175	ORPHA:1988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000347	ORPHA:1988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0003097	ORPHA:1988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000202	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000219	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000343	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000369	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000582	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0001385	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0001762	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0001841	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0002644	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0002812	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0002991	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0003196	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0003422	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0004322	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0005107	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0005772	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0008551	ORPHA:1988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0009800	ORPHA:1988	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000023	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000028	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000040	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000113	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000486	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000772	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000902	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0000912	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0002119	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0002650	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0002974	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0007370	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0008678	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0030680	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1988	Femoral-facial syndrome		HP:0100542	ORPHA:1988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1986	Gollop-Wolfgang complex		HP:0004058	ORPHA:1986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1986	Gollop-Wolfgang complex		HP:0005772	ORPHA:1986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1986	Gollop-Wolfgang complex		HP:0006495	ORPHA:1986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1986	Gollop-Wolfgang complex		HP:0010443	ORPHA:1986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1986	Gollop-Wolfgang complex		HP:0100257	ORPHA:1986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000122	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000286	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000347	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000358	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000396	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000470	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000581	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000592	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000601	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000767	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0000921	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0001177	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0001508	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0001511	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0002092	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0002206	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0002643	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0002650	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0002937	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0004322	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0005950	ORPHA:52047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0005988	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0006610	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52047	Braddock syndrome		HP:0010720	ORPHA:52047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001256	ORPHA:251071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001263	ORPHA:251071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001511	ORPHA:251071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000028	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000047	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000218	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000252	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000286	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000347	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000348	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000369	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000431	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000470	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000708	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001182	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001250	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001510	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001671	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001824	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0002465	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0003196	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0004322	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0004415	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0004422	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0006610	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0006695	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0007018	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000377	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0030680	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0100625	ORPHA:251071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000233	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000293	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000426	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000486	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000490	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000494	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000582	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0000776	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001513	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001636	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001639	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001643	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001669	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001679	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0001763	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0004383	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0009623	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0010059	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251071	8p23.1 microdeletion syndrome		HP:0011304	ORPHA:251071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0001770	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0004209	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0004279	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0004691	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0005048	ORPHA:157801	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0006101	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0008362	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0009701	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0009773	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0009778	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0009843	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157801	Mesoaxial synostotic syndactyly with phalangeal reduction		HP:0010109	ORPHA:157801	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000085	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000160	ORPHA:1973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000175	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000316	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000319	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000411	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000430	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000431	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0000668	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0001249	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0001357	ORPHA:1973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0001508	ORPHA:1973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0001704	ORPHA:1973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1973	Faciocardiorenal syndrome		HP:0001706	ORPHA:1973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0000160	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0000171	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0000308	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0001511	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0001643	ORPHA:1972	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0001852	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0002984	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0003022	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0003038	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0006433	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0004383	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0005736	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0007598	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0009237	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1972	Lethal faciocardiomelic dysplasia		HP:0009778	ORPHA:1972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000028	ORPHA:1970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000046	ORPHA:1970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000164	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000174	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000256	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000280	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000286	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000337	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000348	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000358	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000431	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000545	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000574	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000639	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000648	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0000664	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001007	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001099	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001250	ORPHA:1970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001252	ORPHA:1970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001276	ORPHA:1970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001305	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001821	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0002650	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0004374	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0001249	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0009882	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0010864	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1970	Facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome		HP:0011039	ORPHA:1970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0000045	ORPHA:457083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0012741	ORPHA:457083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0032404	ORPHA:457083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0000023	ORPHA:457083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0000034	ORPHA:457083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0001748	ORPHA:457083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0008689	ORPHA:457083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0009714	ORPHA:457083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0010452	ORPHA:457083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion		HP:0000036	ORPHA:457083	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion	NOT	HP:0000837	ORPHA:457083	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion	NOT	HP:0006254	ORPHA:457083	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457083	Isolated splenogonadal fusion	NOT	HP:0045040	ORPHA:457083	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001298	ORPHA:442835	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000750	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001249	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001250	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001263	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001265	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001290	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001508	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002376	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0010844	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0011443	ORPHA:442835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000252	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000348	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000494	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000508	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000639	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000668	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000708	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000717	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001251	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001257	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001268	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001273	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001315	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001336	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001337	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001558	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002020	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002059	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002063	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002317	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0001288	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002421	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002521	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0004305	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0004322	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0007018	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0011968	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0012444	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0012447	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0100660	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0100710	ORPHA:442835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000504	ORPHA:442835	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000546	ORPHA:442835	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0000648	ORPHA:442835	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002133	ORPHA:442835	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0002509	ORPHA:442835	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:442835	Non-specific early-onset epileptic encephalopathy		HP:0012547	ORPHA:442835	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0000160	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0000271	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0000347	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0000444	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0000767	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0000982	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0001072	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0001371	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0001387	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0001763	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0001824	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0003758	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0004326	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0008065	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0009125	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0100578	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0100679	ORPHA:1979	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0000765	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0001000	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0001595	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0002216	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0002621	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0002814	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0002817	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0003119	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0004349	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0010980	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1979	Lipodystrophy due to peptidic growth factors deficiency		HP:0100651	ORPHA:1979	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0001249	ORPHA:251076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0001263	ORPHA:251076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0002463	ORPHA:251076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0002553	ORPHA:251076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0030680	ORPHA:251076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0000126	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0000316	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0000343	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0000365	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0000445	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0000490	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0000846	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0001629	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0001636	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0001642	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0001770	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0012471	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251076	8p23.1 duplication syndrome		HP:0100777	ORPHA:251076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0000272	ORPHA:52056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0001028	ORPHA:52056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0001156	ORPHA:52056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0001510	ORPHA:52056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0001631	ORPHA:52056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0001762	ORPHA:52056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0001773	ORPHA:52056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0004322	ORPHA:52056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0006210	ORPHA:52056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0006492	ORPHA:52056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0006495	ORPHA:52056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52056	Ulnar/fibula ray defect-brachydactyly syndrome		HP:0009237	ORPHA:52056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0002073	ORPHA:247815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0007002	ORPHA:247815	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0001256	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0001260	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0002070	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0002078	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0007240	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0007256	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0007772	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0008167	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0010965	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0100275	ORPHA:247815	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0001347	ORPHA:247815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0002457	ORPHA:247815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0005978	ORPHA:247815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0011499	ORPHA:247815	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency		HP:0001761	ORPHA:247815	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency	NOT	HP:0000657	ORPHA:247815	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:247815	Autosomal recessive ataxia due to PEX10 deficiency	NOT	HP:0001263	ORPHA:247815	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000049	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000154	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000218	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000232	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000248	ORPHA:1974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000276	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000316	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000325	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000343	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000347	ORPHA:1974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000349	ORPHA:1974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000358	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000396	ORPHA:1974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000426	ORPHA:1974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000463	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000472	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000506	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000582	ORPHA:1974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000637	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0000974	ORPHA:1974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0001156	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0001773	ORPHA:1974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0002002	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0002007	ORPHA:1974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0002208	ORPHA:1974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0003196	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0004209	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0004322	ORPHA:1974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0005599	ORPHA:1974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0001382	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0006101	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0010807	ORPHA:1974	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0011359	ORPHA:1974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1974	Autosomal recessive faciodigitogenital syndrome		HP:0200021	ORPHA:1974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000175	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000218	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000256	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000278	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000348	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000365	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000369	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000377	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000378	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000407	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000426	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000453	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000470	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000494	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000588	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000612	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000639	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0000767	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0001249	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0001274	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0001629	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0001643	ORPHA:52055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0002650	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52055	Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome		HP:0004322	ORPHA:52055	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0002076	ORPHA:157835	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0002331	ORPHA:157835	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0000508	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0000613	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0002183	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0009926	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0012384	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0030953	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0031284	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0031417	ORPHA:157835	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0000616	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0000819	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0000822	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0002017	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0011161	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0012452	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0025258	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0030833	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania		HP:0100540	ORPHA:157835	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania	NOT	HP:0012199	ORPHA:157835	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:157835	Paroxysmal hemicrania	NOT	HP:0100661	ORPHA:157835	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0003259	ORPHA:439232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0100957	ORPHA:439232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0000822	ORPHA:439232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0001917	ORPHA:439232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0012622	ORPHA:439232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0030872	ORPHA:439232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0032613	ORPHA:439232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0000093	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0000096	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0000819	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0001639	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0001677	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0001712	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0003077	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0003418	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0006510	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0011024	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0011713	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0012664	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0031047	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0031546	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0032092	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0034807	ORPHA:439232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0001688	ORPHA:439232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0002088	ORPHA:439232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0004381	ORPHA:439232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0004749	ORPHA:439232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0005110	ORPHA:439232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0012309	ORPHA:439232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:439232	AApoAIV amyloidosis		HP:0030843	ORPHA:439232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0000044	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001251	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001260	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001332	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001596	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001730	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001761	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001943	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0002342	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0005978	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0007108	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0007256	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0008734	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0008897	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0008994	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0030341	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0030344	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0040171	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0100287	ORPHA:453533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0001321	ORPHA:453533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0010627	ORPHA:453533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0011787	ORPHA:453533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453533	Polyendocrine-polyneuropathy syndrome		HP:0040216	ORPHA:453533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1962	Exostoses-anetodermia-brachydactyly type E syndrome		HP:0002762	ORPHA:1962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1962	Exostoses-anetodermia-brachydactyly type E syndrome		HP:0004334	ORPHA:1962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1962	Exostoses-anetodermia-brachydactyly type E syndrome		HP:0005863	ORPHA:1962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1962	Exostoses-anetodermia-brachydactyly type E syndrome		HP:0008065	ORPHA:1962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1962	Exostoses-anetodermia-brachydactyly type E syndrome		HP:0012733	ORPHA:1962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0002213	ORPHA:90368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0100038	ORPHA:90368	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0000962	ORPHA:90368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0001036	ORPHA:90368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0002209	ORPHA:90368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0002293	ORPHA:90368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0025092	ORPHA:90368	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0000989	ORPHA:90368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0001047	ORPHA:90368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0003193	ORPHA:90368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0003212	ORPHA:90368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp		HP:0040189	ORPHA:90368	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0000164	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0000499	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0000534	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0001597	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0002550	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0004528	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0007550	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0100133	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90368	Hypotrichosis simplex of the scalp	NOT	HP:0100134	ORPHA:90368	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0000463	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0000508	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0000767	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0000820	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0000995	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0001555	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0001608	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0001633	ORPHA:1969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0002039	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0002650	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0002808	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0002970	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0003202	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0004122	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0004322	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0004326	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0006101	ORPHA:1969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0007513	ORPHA:1969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0007565	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0007703	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1969	Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome		HP:0010290	ORPHA:1969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000160	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000272	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000276	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000337	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000343	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000347	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000348	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000400	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000430	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000431	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000506	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000581	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0001611	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0002553	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0002705	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0002714	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0003189	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0009738	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0009896	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0009906	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0009912	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0010669	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0010751	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0012368	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0045075	ORPHA:1968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000023	ORPHA:1968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000028	ORPHA:1968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000046	ORPHA:1968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0000358	ORPHA:1968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0002650	ORPHA:1968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0011830	ORPHA:1968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1968	Flat face-microstomia-ear anomaly syndrome		HP:0100490	ORPHA:1968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000027	ORPHA:251066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000028	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000044	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000135	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000218	ORPHA:251066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000252	ORPHA:251066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000286	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000316	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000347	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000458	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000482	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000556	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000581	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000582	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000612	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000639	ORPHA:251066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000864	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000960	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001249	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001250	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001263	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001510	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001631	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001634	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001643	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001744	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001762	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0001878	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0004322	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0004444	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0004467	ORPHA:251066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0005280	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0005815	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0000377	ORPHA:251066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0008736	ORPHA:251066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251066	8p11.2 deletion syndrome		HP:0011968	ORPHA:251066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0001075	ORPHA:79100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0004426	ORPHA:79100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0007515	ORPHA:79100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0011124	ORPHA:79100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0100276	ORPHA:79100	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0000306	ORPHA:79100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0007502	ORPHA:79100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0045059	ORPHA:79100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0100277	ORPHA:79100	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0000290	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0000464	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0000708	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0000989	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0001067	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0010783	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0012531	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79100	Atrophoderma vermiculata		HP:0012722	ORPHA:79100	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000708	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0001249	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0001250	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0001263	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002921	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0003080	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0003137	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0008358	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0012379	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0012402	ORPHA:79101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000750	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002154	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002197	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002317	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002360	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002922	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0003348	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0003394	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0003546	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0008326	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0011199	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0012432	ORPHA:79101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000083	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000496	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000511	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000597	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000716	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000718	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000729	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000736	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000738	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0000739	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0001284	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0001289	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0001298	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0001345	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002014	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002015	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002027	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002133	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002373	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002490	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0002936	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0003326	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0009088	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0009830	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0010819	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0011152	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0011342	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0011968	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79101	Hyperprolinemia type 2		HP:0012534	ORPHA:79101	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0000969	ORPHA:90362	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001903	ORPHA:90362	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002593	ORPHA:90362	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0005387	ORPHA:90362	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0012719	ORPHA:90362	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0100766	ORPHA:90362	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001510	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001824	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001888	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002028	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0003073	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0003075	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0004313	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0011472	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0100508	ORPHA:90362	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001281	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001541	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001698	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002027	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002202	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002720	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002850	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002901	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0002917	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0003394	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0004315	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0007430	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0025624	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0001541	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0031686	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0031690	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0045080	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0100512	ORPHA:90362	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0032160	ORPHA:90362	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90362	Primary intestinal lymphangiectasia		HP:0032215	ORPHA:90362	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0000836	ORPHA:79102	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0008153	ORPHA:79102	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0012726	ORPHA:79102	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0000975	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0001513	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0001962	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0002445	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0002917	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0003457	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0003470	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0003752	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0004303	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0007340	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0008180	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0008285	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0011784	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0011785	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0011786	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0012240	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0012364	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0100647	ORPHA:79102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0000016	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0001265	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0001337	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0001824	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0002019	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0003201	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0003394	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0003552	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0009020	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0011998	ORPHA:79102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0001657	ORPHA:79102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0001663	ORPHA:79102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0003694	ORPHA:79102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0005165	ORPHA:79102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0011706	ORPHA:79102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0000597	ORPHA:79102	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0002153	ORPHA:79102	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis		HP:0002203	ORPHA:79102	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis	NOT	HP:0002486	ORPHA:79102	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis	NOT	HP:0003134	ORPHA:79102	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79102	Thyrotoxic periodic paralysis	NOT	HP:0006670	ORPHA:79102	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0001004	ORPHA:90363	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0031686	ORPHA:90363	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0000969	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0001888	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002024	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002028	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0003146	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0004788	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0011741	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0012378	ORPHA:90363	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0001394	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0001945	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002013	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002202	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002563	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002608	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002665	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002720	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002850	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002960	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0003073	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0004313	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0011848	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0011900	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0012050	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0012281	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0012537	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0031085	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0032064	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0032136	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0032387	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0100324	ORPHA:90363	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0001708	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0001907	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002576	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002580	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002584	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0002719	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0005214	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90363	Secondary intestinal lymphangiectasia		HP:0012191	ORPHA:90363	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0000252	ORPHA:1964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0000316	ORPHA:1964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0000347	ORPHA:1964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0000486	ORPHA:1964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0002750	ORPHA:1964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0004322	ORPHA:1964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0006682	ORPHA:1964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0006689	ORPHA:1964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0007400	ORPHA:1964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0007477	ORPHA:1964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0007598	ORPHA:1964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0009804	ORPHA:1964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1964	Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome		HP:0012722	ORPHA:1964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000750	ORPHA:251061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0011098	ORPHA:251061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0410018	ORPHA:251061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000154	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000256	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000286	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000316	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000327	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000343	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000369	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000448	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000473	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000506	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000729	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000736	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0000752	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0001212	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0001249	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0001260	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0001357	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0001511	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0001611	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0001631	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0002015	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0002020	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0002099	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0002167	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0002205	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0002650	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0002750	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0003202	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0008586	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0008897	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0008936	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0010677	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0011344	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0011382	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0011388	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0011470	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0011474	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0011648	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0012023	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0012146	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0012745	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0012758	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0012811	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0020045	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0025160	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0040022	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251061	7q31 microdeletion syndrome		HP:0040326	ORPHA:251061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0000062	ORPHA:206484	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0000137	ORPHA:206484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0000149	ORPHA:206484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0001007	ORPHA:206484	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0002027	ORPHA:206484	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0003270	ORPHA:206484	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0008730	ORPHA:206484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0008723	ORPHA:206484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0008703	ORPHA:206484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0030088	ORPHA:206484	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206484	Gonadoblastoma		HP:0100621	ORPHA:206484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0002266	ORPHA:1949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0007359	ORPHA:1949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0011167	ORPHA:1949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0011188	ORPHA:1949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0032807	ORPHA:1949	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0002104	ORPHA:1949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0002169	ORPHA:1949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0010818	ORPHA:1949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0011154	ORPHA:1949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0032556	ORPHA:1949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0045084	ORPHA:1949	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0002020	ORPHA:1949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0008936	ORPHA:1949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0011171	ORPHA:1949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0011468	ORPHA:1949	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0002133	ORPHA:1949	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1949	Self-limited neonatal epilepsy		HP:0031535	ORPHA:1949	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0000164	ORPHA:1951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0000343	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0000463	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0000524	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0001249	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0001250	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0002720	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0004313	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0004322	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1951	Epilepsy-telangiectasia syndrome		HP:0009237	ORPHA:1951	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0008231	ORPHA:189427	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0002920	ORPHA:189427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0500011	ORPHA:189427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000712	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000716	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000787	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000822	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000858	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000939	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000978	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0001007	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0001050	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0001065	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0001952	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0003077	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0003118	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0003466	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0003701	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0007126	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0012030	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0012743	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0025383	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0031077	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0031845	ORPHA:189427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000725	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0001061	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0001397	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0001596	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0002354	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0002659	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0004324	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0100754	ORPHA:189427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0000859	ORPHA:189427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0002858	ORPHA:189427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0002893	ORPHA:189427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0005584	ORPHA:189427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0008200	ORPHA:189427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0100543	ORPHA:189427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:189427	Cushing syndrome due to bilateral macronodular adrenocortical disease		HP:0100634	ORPHA:189427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000707	ORPHA:48818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0003281	ORPHA:48818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0004840	ORPHA:48818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0005505	ORPHA:48818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0012379	ORPHA:48818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0025498	ORPHA:48818	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000546	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000608	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000819	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0001251	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0001260	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0001332	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0002066	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0002070	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0002072	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0004305	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0007703	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0010837	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0011967	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0012465	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0040303	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0100543	ORPHA:48818	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000273	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000473	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000639	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000643	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0000741	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0001300	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0001337	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0001635	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0002063	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0002304	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0002354	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0010994	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0012090	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0012179	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0012675	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0012696	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia		HP:0100321	ORPHA:48818	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia	NOT	HP:0001394	ORPHA:48818	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:48818	Aceruloplasminemia	NOT	HP:0001395	ORPHA:48818	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0000347	ORPHA:436182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0000831	ORPHA:436182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0001397	ORPHA:436182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0002155	ORPHA:436182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0008193	ORPHA:436182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0008890	ORPHA:436182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0010620	ORPHA:436182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0000541	ORPHA:436182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436182	Microcephalic primordial dwarfism-insulin resistance syndrome		HP:0007875	ORPHA:436182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0001890	ORPHA:1959	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0001973	ORPHA:1959	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0000967	ORPHA:1959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0001904	ORPHA:1959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0000421	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0000952	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0000978	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0000980	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0001254	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0001324	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0002094	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0012378	ORPHA:1959	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1959	Evans syndrome		HP:0001279	ORPHA:1959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0100570	ORPHA:100093	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0002574	ORPHA:100093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0004385	ORPHA:100093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0006722	ORPHA:100093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0006723	ORPHA:100093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0025474	ORPHA:100093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0030166	ORPHA:100093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0001708	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0001962	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0002017	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0002099	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0002730	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0002910	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0003144	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0005180	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0007380	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0009926	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:4000007	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0030148	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0030445	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0031138	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0031417	ORPHA:100093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0002605	ORPHA:100093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0002668	ORPHA:100093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0003198	ORPHA:100093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0030145	ORPHA:100093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100093	Carcinoid syndrome		HP:0030446	ORPHA:100093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000252	ORPHA:251056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000407	ORPHA:251056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001256	ORPHA:251056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001263	ORPHA:251056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000218	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000272	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000286	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000316	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000358	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000377	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000431	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000478	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000494	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000504	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001274	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001357	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001508	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0004322	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0012639	ORPHA:251056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000175	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000343	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000347	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0000582	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001250	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001252	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001319	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0001838	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0002119	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0003241	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0004209	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0030680	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251056	6q25.2q25.3 microdeletion syndrome		HP:0100490	ORPHA:251056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0000324	ORPHA:1955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0000486	ORPHA:1955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0000639	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0000958	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0000966	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0001025	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0001260	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0001265	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0001288	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0002073	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0002075	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0002167	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0003011	ORPHA:1955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0012733	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0100022	ORPHA:1955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1955	Spinocerebellar ataxia type 34		HP:0200034	ORPHA:1955	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001875	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001923	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0003348	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0003648	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0005528	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0005561	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0032169	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0032653	ORPHA:699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000083	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000707	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001518	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001627	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001638	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001738	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001744	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001873	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001903	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002151	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002240	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002490	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0008897	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0012040	ORPHA:699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000093	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000365	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000508	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000518	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000580	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000602	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000819	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000821	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000824	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001250	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001251	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001252	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001263	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001392	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001397	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001399	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001510	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001789	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001876	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0001944	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002015	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002028	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002033	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002148	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002376	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002570	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002900	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002901	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002910	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0002917	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0003076	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0003128	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0008936	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0031546	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0032066	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0100732	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0200118	ORPHA:699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000107	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000252	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000639	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000829	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000846	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000953	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000957	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0000992	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0006270	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0006577	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:699	Pearson syndrome		HP:0009099	ORPHA:699	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0000958	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0001025	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0001508	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0001522	ORPHA:1954	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0002024	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0002093	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0003073	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0007381	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1954	Congenital lethal erythroderma		HP:0008064	ORPHA:1954	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0002155	ORPHA:31150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0003146	ORPHA:31150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0000656	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0000958	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0001433	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0002027	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0002460	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0002730	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0003477	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0004943	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0005145	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0007133	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0008404	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0030814	ORPHA:31150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0001349	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0001712	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0001873	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0001903	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0003396	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0010829	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0007957	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31150	Tangier disease		HP:0100546	ORPHA:31150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000164	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000175	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000405	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000407	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000501	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000541	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000559	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000572	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000592	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000939	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000974	ORPHA:90354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000977	ORPHA:90354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0000978	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001119	ORPHA:90354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001131	ORPHA:90354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001166	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001288	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001319	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001385	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001634	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001642	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001763	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001822	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0002650	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0002659	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0003326	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0001382	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0005930	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0009887	ORPHA:90354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0011003	ORPHA:90354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0012385	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0100689	ORPHA:90354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0100790	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90354	Brittle cornea syndrome		HP:0200020	ORPHA:90354	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0000601	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0001643	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0002683	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0002970	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0003417	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0005716	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0006487	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0010655	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0011849	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1952	Epiphyseal stippling-osteoclastic hyperplasia syndrome		HP:0100670	ORPHA:1952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000164	ORPHA:576283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001249	ORPHA:576283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001263	ORPHA:576283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001999	ORPHA:576283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000175	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000219	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000319	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000324	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000343	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000347	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000490	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000504	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000708	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000729	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000924	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000938	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001344	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002307	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002342	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002360	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002500	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0007018	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0008872	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0008897	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0008947	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0010864	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0011304	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0012448	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0040082	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0410263	ORPHA:576283	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000193	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000218	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000486	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0000951	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001155	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001250	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001382	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001510	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001601	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0001773	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002015	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002020	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002465	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0002608	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0004209	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0011147	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0100559	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576283	SATB2-associated syndrome due to a pathogenic variant		HP:0100886	ORPHA:576283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0100574	ORPHA:100086	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0100634	ORPHA:100086	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0001046	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0001082	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0001541	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0001824	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0002018	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0002039	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0002574	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0002730	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0003270	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0005230	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0010638	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0012334	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0012432	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0030948	ORPHA:100086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0004375	ORPHA:100086	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100086	Gallbladder neuroendocrine tumor		HP:0012658	ORPHA:100086	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0001762	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0002061	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0002194	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0002395	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0002751	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0003394	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0003698	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0007020	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0007210	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0008997	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0009046	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0009129	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0012473	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0012531	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0030051	ORPHA:496689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0001249	ORPHA:496689	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0002015	ORPHA:496689	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0003487	ORPHA:496689	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome		HP:0006380	ORPHA:496689	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome	NOT	HP:0001272	ORPHA:496689	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome	NOT	HP:0002059	ORPHA:496689	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:496689	Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome	NOT	HP:0040081	ORPHA:496689	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000712	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000716	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000722	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000726	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001123	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001152	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001249	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001263	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001270	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001347	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001350	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002167	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0003084	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0007018	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0007132	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0009088	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0011504	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0011916	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0025402	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0030051	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0031814	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0031937	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0032014	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0100033	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0100710	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001250	ORPHA:157850	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001345	ORPHA:157850	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002080	ORPHA:157850	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000505	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000546	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001257	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001266	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001288	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001332	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002071	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002505	ORPHA:157850	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000496	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000510	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000580	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000662	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000708	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000938	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001260	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001268	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001300	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0001927	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002063	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002451	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002454	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0002483	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0007994	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0008181	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0009763	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0012045	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0012179	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0012678	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0031959	ORPHA:157850	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000618	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000619	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157850	Pantothenate kinase-associated neurodegeneration		HP:0000648	ORPHA:157850	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0005227	ORPHA:454840	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0002858	ORPHA:454840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0003002	ORPHA:454840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0003003	ORPHA:454840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0008069	ORPHA:454840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0009725	ORPHA:454840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0012114	ORPHA:454840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0100743	ORPHA:454840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0000138	ORPHA:454840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0002671	ORPHA:454840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0002860	ORPHA:454840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0006725	ORPHA:454840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0006771	ORPHA:454840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0012539	ORPHA:454840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454840	NTHL1-related polyposis		HP:0031287	ORPHA:454840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0000486	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0000491	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0000742	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0001328	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0002188	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0002754	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0002757	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0007021	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0008000	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0010830	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0011344	ORPHA:453510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0000324	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0000347	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0000448	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0001518	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0001562	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0001772	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0001838	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0001999	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0002069	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0002982	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0008780	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0008947	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0009826	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0010841	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0011470	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0012044	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0012745	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453510	Congenital insensitivity to pain with severe intellectual disability		HP:0200020	ORPHA:453510	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0030746	ORPHA:169805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0100310	ORPHA:169805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0001892	ORPHA:169805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0003125	ORPHA:169805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0003645	ORPHA:169805	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0000225	ORPHA:169805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0001933	ORPHA:169805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0002829	ORPHA:169805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0005261	ORPHA:169805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0011889	ORPHA:169805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0012233	ORPHA:169805	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0000790	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0001376	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0001386	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0002170	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0002239	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0002315	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0003040	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0004846	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0006298	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0100309	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0100769	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0100773	ORPHA:169805	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0001250	ORPHA:169805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0003273	ORPHA:169805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:169805	Moderate hemophilia A		HP:0007420	ORPHA:169805	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0011355	ORPHA:69745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0011368	ORPHA:69745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0031285	ORPHA:69745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0100792	ORPHA:69745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0000464	ORPHA:69745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0001965	ORPHA:69745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0025103	ORPHA:69745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0025512	ORPHA:69745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0030350	ORPHA:69745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0200016	ORPHA:69745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0031445	ORPHA:69745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0410340	ORPHA:69745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0001231	ORPHA:69745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0001892	ORPHA:69745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0006477	ORPHA:69745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0012881	ORPHA:69745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0030416	ORPHA:69745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0100648	ORPHA:69745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69745	Warty dyskeratoma		HP:0100737	ORPHA:69745	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000973	ORPHA:90348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000974	ORPHA:90348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001582	ORPHA:90348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0007522	ORPHA:90348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0025167	ORPHA:90348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0100678	ORPHA:90348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000023	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001382	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001653	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001659	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001999	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0004942	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0007495	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0010674	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0100790	ORPHA:90348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000015	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000252	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000270	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000325	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000337	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000369	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000411	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000486	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000508	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000519	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001181	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001252	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001263	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001270	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001348	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001511	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001635	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001680	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002097	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002110	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002256	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002650	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002827	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0004969	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0005989	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0006698	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0007957	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0008897	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0010648	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0011220	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0011950	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0011968	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0012330	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0100512	ORPHA:90348	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000122	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000729	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0000938	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001762	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001763	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0001884	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002013	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002645	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002677	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90348	Autosomal dominant cutis laxa		HP:0002816	ORPHA:90348	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0001249	ORPHA:439218	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0001263	ORPHA:439218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002500	ORPHA:439218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0010818	ORPHA:439218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0010851	ORPHA:439218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0200134	ORPHA:439218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0000980	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0001041	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0001250	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0001252	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0001332	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002104	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002181	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002453	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002540	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0007015	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0011097	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0011968	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0012736	ORPHA:439218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002059	ORPHA:439218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002079	ORPHA:439218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439218	KCNQ2-related developmental and epileptic encephalopathy		HP:0002521	ORPHA:439218	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000953	ORPHA:465508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0003281	ORPHA:465508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0011031	ORPHA:465508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0012463	ORPHA:465508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0002027	ORPHA:465508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0002240	ORPHA:465508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0003040	ORPHA:465508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0003074	ORPHA:465508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0003199	ORPHA:465508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0007574	ORPHA:465508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0012378	ORPHA:465508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000029	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000044	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000141	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000771	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000789	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000819	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000821	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000939	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001254	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001324	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001369	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001386	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001387	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001394	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001402	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001409	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001635	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001638	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001640	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001744	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0001824	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0002829	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0005198	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0009830	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0011911	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0030848	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0040171	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0046504	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0100626	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0100639	ORPHA:465508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0000741	ORPHA:465508	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0011675	ORPHA:465508	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:465508	Symptomatic form of HFE-related hemochromatosis		HP:0030153	ORPHA:465508	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0000973	ORPHA:90349	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0001582	ORPHA:90349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002097	ORPHA:90349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0010750	ORPHA:90349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0025167	ORPHA:90349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0100679	ORPHA:90349	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0000023	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0000271	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0001270	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0001382	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0001511	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0001635	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0001999	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002093	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002107	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002756	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0004426	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0004969	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0011004	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0030680	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0032153	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0045027	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0100790	ORPHA:90349	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0000010	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0000076	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0000929	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002021	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002256	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002617	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0002827	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0004381	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0006532	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0006698	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0008722	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0012330	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0012619	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90349	Autosomal recessive cutis laxa type 1		HP:0030872	ORPHA:90349	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0003125	ORPHA:169802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0003645	ORPHA:169802	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0000421	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0000978	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0001058	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0001386	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0001934	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0004846	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0005261	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0030140	ORPHA:169802	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0000132	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0001376	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0001903	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0002170	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0002239	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0002315	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0002829	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0003121	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0005187	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0008330	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0012233	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0012541	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0012587	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0030137	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0100309	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0100310	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:169802	Severe hemophilia A		HP:0100769	ORPHA:169802	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0000110	ORPHA:294415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0002240	ORPHA:294415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0000083	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0000105	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0000107	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001562	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0002643	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0002904	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0005232	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0006566	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0030146	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0030948	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0030992	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0031956	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0031964	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0100651	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0100732	ORPHA:294415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0000104	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0000952	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001394	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001395	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001407	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001642	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001643	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001650	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001737	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001744	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001746	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0001790	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0002089	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0003312	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0004890	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0033478	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:294415	Renal-hepatic-pancreatic dysplasia		HP:0410288	ORPHA:294415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1948	Epilepsy-microcephaly-skeletal dysplasia syndrome		HP:0000252	ORPHA:1948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1948	Epilepsy-microcephaly-skeletal dysplasia syndrome		HP:0001007	ORPHA:1948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1948	Epilepsy-microcephaly-skeletal dysplasia syndrome		HP:0001249	ORPHA:1948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1948	Epilepsy-microcephaly-skeletal dysplasia syndrome		HP:0001250	ORPHA:1948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1948	Epilepsy-microcephaly-skeletal dysplasia syndrome		HP:0000280	ORPHA:1948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1948	Epilepsy-microcephaly-skeletal dysplasia syndrome		HP:0002650	ORPHA:1948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1948	Epilepsy-microcephaly-skeletal dysplasia syndrome		HP:0002750	ORPHA:1948	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000078	ORPHA:251046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000126	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000174	ORPHA:251046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000238	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000286	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000365	ORPHA:251046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000369	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000396	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000470	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000486	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000490	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000601	ORPHA:251046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0000929	ORPHA:251046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0001252	ORPHA:251046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0001256	ORPHA:251046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0001582	ORPHA:251046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0001643	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0006101	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0012639	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0030084	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251046	6p22 microdeletion syndrome		HP:0100790	ORPHA:251046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0100570	ORPHA:100082	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0001824	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002019	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002027	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002039	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002240	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002573	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002730	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002910	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0012702	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0025085	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0030144	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0030446	ORPHA:100082	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0001708	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0001962	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002249	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0002615	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0003144	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0004385	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0005180	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0007380	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0012701	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:4000007	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0030145	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100082	Neuroendocrine tumor of anal canal		HP:0031566	ORPHA:100082	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0100605	ORPHA:100083	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0100634	ORPHA:100083	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0001618	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0001824	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0002039	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0002730	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0002875	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0003144	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0003528	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0012432	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0200136	ORPHA:100083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0011749	ORPHA:100083	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0031029	ORPHA:100083	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100083	Laryngeal neuroendocrine tumor		HP:0031218	ORPHA:100083	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0011471	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0012690	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0030890	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000505	ORPHA:1947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0001249	ORPHA:1947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0001250	ORPHA:1947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0001272	ORPHA:1947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002540	ORPHA:1947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0003204	ORPHA:1947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0003657	ORPHA:1947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000529	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000543	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000550	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000750	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0001251	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002059	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002066	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002123	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002167	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002312	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002317	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002333	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002371	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002510	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0003205	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0003208	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0003698	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0005268	ORPHA:1947	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0011198	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0011203	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0030455	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0033044	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0100543	ORPHA:1947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000708	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000726	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0000729	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0001263	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002015	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002359	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1947	Northern epilepsy		HP:0002384	ORPHA:1947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0000238	ORPHA:1946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0000966	ORPHA:1946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0001250	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0001257	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0001268	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0002353	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0002376	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0004322	ORPHA:1946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0006286	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0011073	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0000682	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0000705	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0000726	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1946	Amelocerebrohypohidrotic syndrome		HP:0010864	ORPHA:1946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0100570	ORPHA:100084	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0100634	ORPHA:100084	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0040119	ORPHA:100084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0040090	ORPHA:100084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0000360	ORPHA:100084	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0000372	ORPHA:100084	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0000407	ORPHA:100084	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0002730	ORPHA:100084	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0002028	ORPHA:100084	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0002315	ORPHA:100084	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100084	Middle ear neuroendocrine tumor		HP:0010628	ORPHA:100084	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000491	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000953	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000988	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001094	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001376	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001386	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0002829	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0005764	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0010783	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0012123	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0012647	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0100769	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0200034	ORPHA:90340	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000501	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000518	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000613	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000958	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001369	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001945	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0012219	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0100490	ORPHA:90340	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000112	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000217	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000488	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000572	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000587	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000610	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0000822	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001291	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001392	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001701	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001744	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0001903	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0002092	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0002094	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0002716	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0003774	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0004942	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0005310	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0006770	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0008046	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0008064	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0010286	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0010628	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0100654	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90340	Blau syndrome		HP:0200042	ORPHA:90340	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0000508	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0001046	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0004375	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0005230	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002896	ORPHA:100085	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0100634	ORPHA:100085	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0001541	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0001824	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002014	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002018	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002039	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002094	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002240	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002574	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002730	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002910	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0003270	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0012432	ORPHA:100085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0001407	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0001708	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0001962	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0002480	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0003144	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0007380	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:4000007	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0025474	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0030148	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0030166	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0100570	ORPHA:100085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0006575	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0007663	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0010638	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0012658	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0030948	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0100012	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma		HP:0100526	ORPHA:100085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma	NOT	HP:0006254	ORPHA:100085	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100085	Primary hepatic neuroendocrine carcinoma	NOT	HP:0031029	ORPHA:100085	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0012557	ORPHA:1945	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0002307	ORPHA:1945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0007332	ORPHA:1945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0007334	ORPHA:1945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0007359	ORPHA:1945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0009088	ORPHA:1945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0010535	ORPHA:1945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0025425	ORPHA:1945	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0000712	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0000716	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0000736	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0000739	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0001328	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0002076	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0002373	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0003401	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0006889	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0007018	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0012534	ORPHA:1945	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0001326	ORPHA:1945	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1945	Self-limited epilepsy with centrotemporal spikes		HP:0007270	ORPHA:1945	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0000491	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0000613	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0000953	ORPHA:90342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0000958	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0000992	ORPHA:90342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0001009	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0001010	ORPHA:90342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0001029	ORPHA:90342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0002671	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0002860	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0002861	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0004334	ORPHA:90342	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90342	Xeroderma pigmentosum variant		HP:0007603	ORPHA:90342	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0100570	ORPHA:100080	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0001824	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0002027	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0002039	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0002240	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0002730	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0025085	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0030144	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0030446	ORPHA:100080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0001708	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0001962	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0002249	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0002615	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0002910	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0003144	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0004385	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0005180	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0007380	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0012701	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:4000007	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0030145	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100080	Neuroendocrine tumor of the colon		HP:0031566	ORPHA:100080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0011170	ORPHA:1942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0011197	ORPHA:1942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000752	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001249	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0002121	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0002123	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0002332	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0002392	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0007018	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0010819	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0025190	ORPHA:1942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000729	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0012760	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001251	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001326	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001337	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0010845	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0011171	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0011182	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0100851	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0410263	ORPHA:1942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000154	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000179	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000219	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000252	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000289	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000343	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000431	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000463	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000568	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0000750	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001159	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001252	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001263	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0001999	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0002292	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0002317	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0007256	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0007359	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0009928	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0011220	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0100678	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures		HP:0200134	ORPHA:1942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1942	Epilepsy with myoclonic-atonic seizures	NOT	HP:0011097	ORPHA:1942	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0002133	ORPHA:1941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0002373	ORPHA:1941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0032794	ORPHA:1941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0100851	ORPHA:1941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0002069	ORPHA:1941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0002197	ORPHA:1941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0002392	ORPHA:1941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0000153	ORPHA:1941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0000496	ORPHA:1941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0001336	ORPHA:1941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0002121	ORPHA:1941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0000739	ORPHA:1941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1941	Juvenile absence epilepsy		HP:0001328	ORPHA:1941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0100570	ORPHA:100081	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0001824	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002019	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002027	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002039	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002573	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0012702	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0025085	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0030144	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0030446	ORPHA:100081	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002240	ORPHA:100081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002249	ORPHA:100081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002730	ORPHA:100081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002910	ORPHA:100081	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0001708	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0001962	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0002615	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0003144	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0004385	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0005180	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0007380	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0012701	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:4000007	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0030145	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100081	Neuroendocrine tumor of the rectum		HP:0031566	ORPHA:100081	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0006723	ORPHA:100079	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002017	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002574	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0004396	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0005249	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0010676	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0011848	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0012701	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0030142	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0030144	ORPHA:100079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002019	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002039	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002240	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002730	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002910	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0003148	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0004385	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0030412	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0040276	ORPHA:100079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0001579	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0001962	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002099	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0002615	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0003144	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0005211	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0010446	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0011749	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0030148	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0031499	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100079	Neuroendocrine neoplasm of appendix		HP:0100615	ORPHA:100079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0100570	ORPHA:100075	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0001824	ORPHA:100075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0001891	ORPHA:100075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002017	ORPHA:100075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002039	ORPHA:100075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002254	ORPHA:100075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002574	ORPHA:100075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0004396	ORPHA:100075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0001005	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002044	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002240	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002248	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002249	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002730	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002910	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0025085	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0030145	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0030446	ORPHA:100075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0001399	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0001708	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0001962	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002615	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0002668	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0003144	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0003154	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0004385	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0005180	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0007380	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0012701	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:4000007	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0030149	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100075	Neuroendocrine tumor of stomach		HP:0031566	ORPHA:100075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0004302	ORPHA:1929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0007359	ORPHA:1929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0001269	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002119	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002349	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002384	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002960	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0004305	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0011153	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0011193	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0011195	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0012157	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0012847	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0032665	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0100308	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0100543	ORPHA:1929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0000572	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0000708	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0000712	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0000737	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0000752	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0001260	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0001328	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002134	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002354	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002381	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002540	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002921	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002922	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0003493	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0007018	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0007334	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0010818	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0011163	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0011182	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0011185	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0012708	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0020151	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0025190	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0031491	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0031535	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0032005	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0032046	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0100660	ORPHA:1929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0002283	ORPHA:1929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0003460	ORPHA:1929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0011097	ORPHA:1929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1929	Rasmussen subacute encephalitis		HP:0032661	ORPHA:1929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0002097	ORPHA:1928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0002098	ORPHA:1928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0000961	ORPHA:1928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0001649	ORPHA:1928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0002094	ORPHA:1928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0010978	ORPHA:1928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0030828	ORPHA:1928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:6000012	ORPHA:1928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0001508	ORPHA:1928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0001555	ORPHA:1928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0011968	ORPHA:1928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0030680	ORPHA:1928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1928	Congenital lobar emphysema		HP:0100750	ORPHA:1928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0000218	ORPHA:1927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0000343	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0000348	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0001156	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0001172	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0001319	ORPHA:1927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0002162	ORPHA:1927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0005280	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0006070	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0009626	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0012368	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1927	Emery-Nelson syndrome		HP:0100490	ORPHA:1927	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0006722	ORPHA:100078	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0001005	ORPHA:100078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002254	ORPHA:100078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002574	ORPHA:100078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0003144	ORPHA:100078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0001824	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0001891	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002018	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002572	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002716	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002910	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0003148	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0004796	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0005249	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0012334	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0012432	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0025324	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0030142	ORPHA:100078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0100819	ORPHA:100078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0000126	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0000969	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0001399	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0001642	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0001708	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0001962	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002044	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0002615	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0010446	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0011675	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0025426	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100078	Ileal neuroendocrine tumor		HP:0030149	ORPHA:100078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001332	ORPHA:157846	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002134	ORPHA:157846	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0012343	ORPHA:157846	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0012675	ORPHA:157846	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0100543	ORPHA:157846	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0000338	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0000712	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001260	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001618	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002015	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002067	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002072	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002310	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002339	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001288	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002454	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0004305	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0004373	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0012678	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0012690	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0012696	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0031959	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0031982	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0100321	ORPHA:157846	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0000643	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001300	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001348	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001621	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0001686	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002340	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002356	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002395	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0007350	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0007772	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0010530	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0031960	ORPHA:157846	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0000709	ORPHA:157846	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0000727	ORPHA:157846	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002322	ORPHA:157846	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0002922	ORPHA:157846	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0003487	ORPHA:157846	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0007123	ORPHA:157846	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157846	Neuroferritinopathy		HP:0025331	ORPHA:157846	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0001284	ORPHA:231445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0002385	ORPHA:231445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0003477	ORPHA:231445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0006858	ORPHA:231445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0011868	ORPHA:231445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0012531	ORPHA:231445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0025459	ORPHA:231445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0011096	ORPHA:231445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome		HP:0011948	ORPHA:231445	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231445	Paraparetic variant of Guillain-Barré syndrome	NOT	HP:0002839	ORPHA:231445	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0001917	ORPHA:439224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0012280	ORPHA:439224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0000083	ORPHA:439224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0000093	ORPHA:439224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0000822	ORPHA:439224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0003259	ORPHA:439224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0033247	ORPHA:439224	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0000853	ORPHA:439224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0002910	ORPHA:439224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0012145	ORPHA:439224	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439224	ALECT2 amyloidosis		HP:0002907	ORPHA:439224	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0000657	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0000664	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0000666	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0000750	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0001260	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0001263	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0001310	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0001320	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0001332	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0001350	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002066	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002078	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002080	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002312	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002317	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002342	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002359	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0002470	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0003487	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0008947	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0009617	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0031435	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0040196	ORPHA:453521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		HP:0001274	ORPHA:453521	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000164	ORPHA:251038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000175	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000218	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000239	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000252	ORPHA:251038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000256	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000348	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000365	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000369	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000431	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000470	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000494	ORPHA:251038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000518	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000526	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000568	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000612	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0000647	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001249	ORPHA:251038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001250	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001252	ORPHA:251038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001263	ORPHA:251038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001363	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001513	ORPHA:251038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001629	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001770	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001836	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0001852	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0002002	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0004397	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251038	3q29 microduplication syndrome		HP:0004422	ORPHA:251038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0000767	ORPHA:1937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0001156	ORPHA:1937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0001369	ORPHA:1937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0001511	ORPHA:1937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0001629	ORPHA:1937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0001671	ORPHA:1937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0002650	ORPHA:1937	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0004322	ORPHA:1937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1937	Eng-Strom syndrome		HP:0100490	ORPHA:1937	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:57782	Mazabraud syndrome		HP:0000924	ORPHA:57782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57782	Mazabraud syndrome		HP:0002652	ORPHA:57782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57782	Mazabraud syndrome		HP:0002653	ORPHA:57782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57782	Mazabraud syndrome		HP:0002757	ORPHA:57782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:57782	Mazabraud syndrome		HP:0010734	ORPHA:57782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0000763	ORPHA:100073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0000772	ORPHA:100073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0001324	ORPHA:100073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0002829	ORPHA:100073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0003326	ORPHA:100073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0003401	ORPHA:100073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0003457	ORPHA:100073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100073	Neurogenic thoracic outlet syndrome		HP:0012534	ORPHA:100073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001250	ORPHA:1934	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001249	ORPHA:1934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001263	ORPHA:1934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002123	ORPHA:1934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0011153	ORPHA:1934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0200134	ORPHA:1934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001254	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001347	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002015	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002033	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002205	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002353	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002360	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002421	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002521	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0008947	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0010851	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0011167	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0011968	ORPHA:1934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000729	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000752	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001257	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001266	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001272	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001302	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001336	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001337	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002069	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002079	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002121	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002131	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002373	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002376	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0002506	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0007204	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0007359	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0010818	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0010819	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0010850	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0011169	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0011190	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0012448	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0012469	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0100660	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0100716	ORPHA:1934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000054	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000070	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000110	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000175	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000252	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000340	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000463	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000486	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0000826	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001332	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001500	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001508	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001537	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0001629	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0005280	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0009381	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0010174	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1934	Early infantile developmental and epileptic encephalopathy		HP:0012554	ORPHA:1934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000252	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000407	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000505	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000508	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000512	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000649	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000708	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0000762	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0001250	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0001251	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0001263	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0001265	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0002119	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0002194	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0002230	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0002514	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0003202	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0003236	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0003355	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0004322	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0004326	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0001249	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1933	Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria		HP:0012120	ORPHA:1933	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0000238	ORPHA:1931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0000256	ORPHA:1931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0000268	ORPHA:1931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0000316	ORPHA:1931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0001250	ORPHA:1931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0001362	ORPHA:1931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0002084	ORPHA:1931	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0002414	ORPHA:1931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0002415	ORPHA:1931	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0002514	ORPHA:1931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1931	Frontal encephalocele		HP:0007370	ORPHA:1931	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0000474	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0001268	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002145	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002354	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002381	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0006892	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0006977	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0007112	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0030391	ORPHA:100070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0000716	ORPHA:100070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0000739	ORPHA:100070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002186	ORPHA:100070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002500	ORPHA:100070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0010523	ORPHA:100070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0011204	ORPHA:100070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0012658	ORPHA:100070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0000708	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0000711	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0000751	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0001300	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002071	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002300	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002366	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002427	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0002446	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0010526	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0030223	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia		HP:0100256	ORPHA:100070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia	NOT	HP:0001297	ORPHA:100070	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia	NOT	HP:0002185	ORPHA:100070	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia	NOT	HP:0030692	ORPHA:100070	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100070	Progressive non-fluent aphasia	NOT	HP:0100315	ORPHA:100070	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002353	ORPHA:1930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0004372	ORPHA:1930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0012443	ORPHA:1930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0200149	ORPHA:1930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0001250	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0001945	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0001974	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002017	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002167	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002315	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002902	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002922	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0004887	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0007185	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0011897	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0012378	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0031179	ORPHA:1930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0001259	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0001262	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0001347	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002133	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002181	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002349	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002384	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0002721	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0004302	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0011227	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0011972	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0025143	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1930	Herpes simplex virus encephalitis		HP:0030955	ORPHA:1930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0001903	ORPHA:673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0001919	ORPHA:673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0001945	ORPHA:673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0002011	ORPHA:673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0002017	ORPHA:673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0002315	ORPHA:673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0011227	ORPHA:673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0001871	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0001873	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0002098	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0002141	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0002904	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0003326	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0004372	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0100543	ORPHA:673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:673	Malaria		HP:0000488	ORPHA:673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002444	ORPHA:672	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000110	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000191	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000193	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000256	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000316	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000358	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000413	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000457	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000463	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000494	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000508	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000568	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000695	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000902	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001156	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001162	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001511	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001770	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002023	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002164	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002652	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002827	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002937	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002986	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0003048	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0003196	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0004322	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0005917	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0006136	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008213	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008240	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008245	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008551	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008751	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0009958	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0009971	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0010044	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0011304	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0011734	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0011748	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0011939	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0012751	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0040075	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0040086	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0100260	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0200117	ORPHA:672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000023	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000028	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000047	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000054	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000086	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000122	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000171	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000175	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000273	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000308	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000453	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000749	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000826	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000835	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000871	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001263	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001273	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001321	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001360	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001520	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001537	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001629	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001631	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001643	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001680	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001837	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001845	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002101	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0005990	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0006695	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0007601	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008207	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008734	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0010564	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0010821	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0012165	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0030021	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0410030	ORPHA:672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000046	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000062	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0000243	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001249	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001562	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0001883	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002093	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0002139	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0005684	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0008684	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0010958	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0011026	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0030010	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0030431	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:672	Pallister-Hall syndrome		HP:0030799	ORPHA:672	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0002381	ORPHA:100069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0012444	ORPHA:100069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0030222	ORPHA:100069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0030784	ORPHA:100069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0000726	ORPHA:100069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0002167	ORPHA:100069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0010522	ORPHA:100069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0010523	ORPHA:100069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0010526	ORPHA:100069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100069	Semantic dementia		HP:0012671	ORPHA:100069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:675	Annular pancreas		HP:0001734	ORPHA:675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:675	Annular pancreas		HP:0005250	ORPHA:675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:675	Annular pancreas		HP:0100867	ORPHA:675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0000286	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0000303	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0000316	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0000369	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0001156	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0001249	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0001263	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0008386	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0012808	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0100333	ORPHA:1919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0000047	ORPHA:1919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0000252	ORPHA:1919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0000272	ORPHA:1919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0001633	ORPHA:1919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0001636	ORPHA:1919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1919	Phenobarbital embryopathy		HP:0006265	ORPHA:1919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0000028	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0000347	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0000358	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0001537	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0001629	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0002230	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0004209	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1918	Fetal minoxidil syndrome		HP:0005280	ORPHA:1918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1917	Fetal methylmercury syndrome		HP:0000252	ORPHA:1917	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1917	Fetal methylmercury syndrome		HP:0000365	ORPHA:1917	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1917	Fetal methylmercury syndrome		HP:0000505	ORPHA:1917	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1917	Fetal methylmercury syndrome		HP:0001252	ORPHA:1917	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1917	Fetal methylmercury syndrome		HP:0004322	ORPHA:1917	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0000013	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0000028	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0000035	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0000047	ORPHA:1916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0000054	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0000130	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0000868	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0001518	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0001622	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0002861	ORPHA:1916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0003002	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0002871	ORPHA:1916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0008209	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0008715	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0012243	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0030424	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0100602	ORPHA:1916	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:1916	Diethylstilbestrol syndrome		HP:0100650	ORPHA:1916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324723	ABeta amyloidosis, Arctic type		HP:0000708	ORPHA:324723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324723	ABeta amyloidosis, Arctic type		HP:0002373	ORPHA:324723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0001347	ORPHA:320365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0002061	ORPHA:320365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0002064	ORPHA:320365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0003487	ORPHA:320365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0007020	ORPHA:320365	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0000012	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0000020	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0002460	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0003701	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0006858	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0006886	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0006937	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0007220	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0010829	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0011402	ORPHA:320365	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0000486	ORPHA:320365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0001369	ORPHA:320365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36		HP:0001761	ORPHA:320365	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36	NOT	HP:0000726	ORPHA:320365	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:320365	Autosomal dominant spastic paraplegia type 36	NOT	HP:0012747	ORPHA:320365	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0001644	ORPHA:300751	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0031546	ORPHA:300751	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0001279	ORPHA:300751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0001637	ORPHA:300751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0001645	ORPHA:300751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0005110	ORPHA:300751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0005162	ORPHA:300751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0009125	ORPHA:300751	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0001635	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0001698	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0003560	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0004308	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0004749	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0004755	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0012722	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0012723	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300751	Familial dilated cardiomyopathy with conduction defect due to LMNA mutation		HP:0031409	ORPHA:300751	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0000163	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0000708	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0001824	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002076	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002383	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002716	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002829	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002840	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0004370	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0032323	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0100776	ORPHA:42642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0000737	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002307	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002315	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0003326	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0011107	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0012378	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0025289	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0025439	ORPHA:42642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0001369	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0001744	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002017	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002024	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002027	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0002240	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0011110	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42642	PFAPA syndrome		HP:0012514	ORPHA:42642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001263	ORPHA:251028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001344	ORPHA:251028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000164	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000175	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000218	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000252	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000347	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000348	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000426	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000540	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000708	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000718	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001252	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001776	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001999	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002307	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0008070	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0008734	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0008872	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0010864	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0011220	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0011344	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0011470	ORPHA:251028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000028	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000054	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000160	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000201	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000256	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000275	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000276	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000322	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000324	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000343	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000356	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000369	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000444	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000445	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000470	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000478	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000490	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000494	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000589	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000620	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000678	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000689	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000691	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000711	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000712	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000742	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0000938	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001238	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001250	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001276	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001629	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001762	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0001773	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002007	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002011	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002061	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002136	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002213	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002591	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002659	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002761	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002815	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002870	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002938	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0002982	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0003196	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0003241	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0003272	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0004209	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0004482	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0005469	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0006349	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0008897	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0010055	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0011304	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0011339	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0012428	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0020045	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251028	SATB2-associated syndrome due to a chromosomal rearrangement		HP:0200055	ORPHA:251028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0002166	ORPHA:320360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0007020	ORPHA:320360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0012514	ORPHA:320360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0001347	ORPHA:320360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0002061	ORPHA:320360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0001288	ORPHA:320360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0003477	ORPHA:320360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0009053	ORPHA:320360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0000819	ORPHA:320360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0001317	ORPHA:320360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0001638	ORPHA:320360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0003487	ORPHA:320360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0005115	ORPHA:320360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0007256	ORPHA:320360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia		HP:0008969	ORPHA:320360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia	NOT	HP:0000648	ORPHA:320360	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:320360	MT-ATP6-related mitochondrial spastic paraplegia	NOT	HP:0002151	ORPHA:320360	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000044	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000219	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000252	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000316	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000343	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000403	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000430	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000446	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000556	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000637	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0000964	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0001156	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0001290	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0001433	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0001511	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0001795	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0001831	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0001880	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0002079	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0002342	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0002655	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0002656	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0002714	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0002716	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0003273	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0004209	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0004313	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0004322	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0004625	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0005041	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0006532	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0007598	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0008804	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0008828	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0008897	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0011231	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0410170	ORPHA:353298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome		HP:0012817	ORPHA:353298	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353298	Roifman syndrome	NOT	HP:0005419	ORPHA:353298	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000008	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000028	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000054	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000073	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000126	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000175	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000252	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000358	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000464	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0001629	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0001636	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0001669	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0001679	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0003422	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0004414	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0005107	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0008056	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0008551	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0008678	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0010318	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0030680	ORPHA:1926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000098	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000238	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000347	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000365	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0000707	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0001195	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0002007	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0007360	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0007370	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0010301	ORPHA:1926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1926	Diabetic embryopathy		HP:0001732	ORPHA:1926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0000047	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0000453	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0000820	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0000821	ORPHA:1923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0001362	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0001511	ORPHA:1923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0001561	ORPHA:1923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0001629	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0001679	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0001680	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0002032	ORPHA:1923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0002575	ORPHA:1923	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1923	Methimazole embryofetopathy		HP:0100589	ORPHA:1923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000248	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000256	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000269	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000347	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000365	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000410	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000444	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000670	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000682	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000768	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000772	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000883	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000944	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001288	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001511	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002992	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004331	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0005019	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0011073	ORPHA:666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000164	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000239	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000501	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000505	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000592	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000689	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000703	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000739	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000774	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000938	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000939	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000973	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000975	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001382	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001730	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002150	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002505	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002653	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002659	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002757	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002823	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002857	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002953	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002980	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003084	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003100	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003103	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003272	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003312	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003546	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004322	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004349	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004586	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004621	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001382	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0006640	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0007957	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0011314	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0012378	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0030680	ORPHA:666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000023	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000325	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000684	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000767	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000787	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000978	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001371	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001510	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001518	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001537	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001873	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002011	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002015	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002019	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002119	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002645	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002650	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002758	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002808	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002829	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002983	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003083	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003179	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003401	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003474	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004306	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004482	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0005214	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0006487	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0030267	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0030268	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0100661	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0100761	ORPHA:666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000238	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0000639	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001251	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001342	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001634	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0001659	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002089	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002273	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002315	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002512	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002616	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002643	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002647	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0002947	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0003396	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0004942	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0005257	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0005294	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0006824	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0008905	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0010953	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:666	Osteogenesis imperfecta		HP:0012366	ORPHA:666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001723	ORPHA:75566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001880	ORPHA:75566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001977	ORPHA:75566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0031323	ORPHA:75566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001635	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001654	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001712	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001824	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001962	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0002094	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0012378	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0025168	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0031331	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0100749	ORPHA:75566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001653	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001685	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0006685	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0010872	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0011675	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0011712	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0012735	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0025523	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0031295	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0031442	ORPHA:75566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001650	ORPHA:75566	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001659	ORPHA:75566	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75566	Loeffler endocarditis		HP:0001701	ORPHA:75566	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002172	ORPHA:75567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0001288	ORPHA:75567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002359	ORPHA:75567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0000822	ORPHA:75567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0001347	ORPHA:75567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002063	ORPHA:75567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002067	ORPHA:75567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002167	ORPHA:75567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002169	ORPHA:75567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002174	ORPHA:75567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0000020	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0000726	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0000763	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002015	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002120	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002141	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0002362	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0003487	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0007772	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0012452	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75567	Primary progressive freezing gait		HP:0100315	ORPHA:75567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000028	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000126	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000233	ORPHA:1920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000252	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000286	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000319	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000347	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000369	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000411	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0000486	ORPHA:1920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0001182	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0001252	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0001263	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0001347	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0002167	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0003196	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0004322	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0004422	ORPHA:1920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0007477	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0010669	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0012745	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1920	Toluene embryopathy		HP:0100542	ORPHA:1920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0002797	ORPHA:668	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0006489	ORPHA:668	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0000944	ORPHA:668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0001386	ORPHA:668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0003155	ORPHA:668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0006491	ORPHA:668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0012531	ORPHA:668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0025435	ORPHA:668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0045040	ORPHA:668	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0001824	ORPHA:668	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0001945	ORPHA:668	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:668	Osteosarcoma		HP:0002756	ORPHA:668	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0004828	ORPHA:75564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0010972	ORPHA:75564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0000980	ORPHA:75564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001895	ORPHA:75564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001897	ORPHA:75564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0012132	ORPHA:75564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0200143	ORPHA:75564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001231	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001744	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001873	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001931	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0002240	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0002863	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0011447	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0012136	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0012137	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0012143	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0031035	ORPHA:75564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001635	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001875	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001876	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001892	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001894	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001913	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0001974	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0004808	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0005513	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75564	Acquired idiopathic sideroblastic anemia		HP:0005528	ORPHA:75564	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0000107	ORPHA:445038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0000121	ORPHA:445038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0000518	ORPHA:445038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001875	ORPHA:445038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0003535	ORPHA:445038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0011451	ORPHA:445038	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001249	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001252	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001257	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001266	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001272	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001298	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001336	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001347	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001510	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002059	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002071	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002134	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002151	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002179	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002194	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002376	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0005528	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0007153	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0007256	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0011968	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0410256	ORPHA:445038	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0000083	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0000639	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0000821	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001250	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001276	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001397	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001638	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0001998	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002878	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002910	ORPHA:445038	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445038	3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome		HP:0002107	ORPHA:445038	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000238	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000256	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000365	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000388	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000505	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000639	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000649	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000684	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000772	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000774	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000944	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000978	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0000980	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0001337	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0001363	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0001510	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0001641	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0001744	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0001903	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0001939	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002092	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002104	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002148	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002205	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002240	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002257	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002653	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002716	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002757	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0002901	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0004349	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0004370	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0004415	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0005930	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0006323	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0006487	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0006824	ORPHA:667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0007807	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0008066	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0010543	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0010719	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0011002	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:667	Autosomal recessive malignant osteopetrosis		HP:0100022	ORPHA:667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0006685	ORPHA:75565	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001723	ORPHA:75565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0002094	ORPHA:75565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0003115	ORPHA:75565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0012378	ORPHA:75565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001541	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001640	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001678	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001945	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0002240	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0003073	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0004326	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0004395	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0006677	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0011675	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0011712	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0011713	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0012249	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0012398	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0012764	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0025077	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0025168	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0030950	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0031295	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0031664	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0033114	ORPHA:75565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0000520	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001653	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001744	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001880	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0001907	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0004749	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0004755	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0005110	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0005135	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0005180	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0006690	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0010741	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0011663	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0012664	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0030057	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0030149	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0030783	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0030848	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0031595	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0031650	ORPHA:75565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0005145	ORPHA:75565	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:75565	Tropical endomyocardial fibrosis		HP:0031601	ORPHA:75565	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0000112	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0000246	ORPHA:662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0001004	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0001231	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0001806	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0002092	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0002094	ORPHA:662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0002102	ORPHA:662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0002110	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0002205	ORPHA:662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0002664	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0002721	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0003759	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0008388	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0009726	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0011354	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0011367	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0012384	ORPHA:662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0012735	ORPHA:662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0100242	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0100526	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0100574	ORPHA:662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0100797	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:662	Lymphedema with yellow nails		HP:0100798	ORPHA:662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0100665	ORPHA:100057	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0000282	ORPHA:100057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0025018	ORPHA:100057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0002098	ORPHA:100057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0031244	ORPHA:100057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0040315	ORPHA:100057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0100540	ORPHA:100057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0002781	ORPHA:100057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0010783	ORPHA:100057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0011855	ORPHA:100057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema		HP:0012027	ORPHA:100057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema	NOT	HP:0000989	ORPHA:100057	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100057	Renin-angiotensin-aldosterone system-blocker-induced angioedema	NOT	HP:0001025	ORPHA:100057	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0001250	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0001252	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0002093	ORPHA:661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0002251	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0002270	ORPHA:661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0003005	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0003006	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0006747	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0100006	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:661	Congenital central hypoventilation syndrome		HP:0100543	ORPHA:661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0010702	ORPHA:449400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0032300	ORPHA:449400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0001824	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0001945	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0002027	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0002099	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0002960	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0003212	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0003419	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0003493	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0003565	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0011227	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0012393	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0012649	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0012727	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0032061	ORPHA:449400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0000126	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0002647	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0004431	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0004970	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0005214	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0012303	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0031252	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0032230	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449400	IgG4-related aortitis		HP:0430021	ORPHA:449400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001399	ORPHA:664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001744	ORPHA:664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001943	ORPHA:664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001987	ORPHA:664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0003355	ORPHA:664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001250	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001252	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001254	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001259	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001298	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001950	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002033	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002038	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002039	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002045	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002329	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002910	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0003218	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0003572	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0005961	ORPHA:664	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0000716	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0000739	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001328	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0001508	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002572	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0002908	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0003645	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0007018	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:664	Ornithine transcarbamylase deficiency		HP:0031258	ORPHA:664	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0000003	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0000083	ORPHA:1909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0000091	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0000112	ORPHA:1909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0001562	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0001622	ORPHA:1909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0001629	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0001631	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0001638	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0001789	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0001928	ORPHA:1909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1909	Indomethacin embryofetopathy		HP:0002093	ORPHA:1909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281122	Self-improving collodion baby		HP:0001376	ORPHA:281122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281122	Self-improving collodion baby		HP:0008064	ORPHA:281122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0000590	ORPHA:663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0003800	ORPHA:663	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0000508	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0000821	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0001348	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0002091	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0002151	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0002747	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0003200	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0003327	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0003457	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0008180	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0008316	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0009073	ORPHA:663	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0000716	ORPHA:663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia		HP:0001256	ORPHA:663	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:663	Mitochondrial DNA-related progressive external ophthalmoplegia	NOT	HP:0000651	ORPHA:663	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000175	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000238	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000252	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000303	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000316	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000358	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000431	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000520	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001231	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001360	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001511	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000286	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0000347	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001629	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001636	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001696	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001792	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0001883	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0002084	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0002323	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0002435	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0002652	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0002983	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0003027	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0004322	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0004935	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0006101	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0007360	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0007370	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0009601	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0009891	ORPHA:1908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0010301	ORPHA:1908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1908	Aminopterin/methotrexate embryofetopathy		HP:0100335	ORPHA:1908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:281127	Acral self-healing collodion baby		HP:0007514	ORPHA:281127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281127	Acral self-healing collodion baby		HP:0007559	ORPHA:281127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281127	Acral self-healing collodion baby		HP:0010783	ORPHA:281127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281127	Acral self-healing collodion baby		HP:0012098	ORPHA:281127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281127	Acral self-healing collodion baby		HP:0025524	ORPHA:281127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281127	Acral self-healing collodion baby		HP:0100679	ORPHA:281127	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002922	ORPHA:206443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0034322	ORPHA:206443	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000365	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000565	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000572	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000649	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000708	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000762	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001264	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001268	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001270	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001288	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002061	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002312	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002313	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001288	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002359	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002371	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002376	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002493	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002505	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0004302	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0004466	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0007141	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0009830	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0010846	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0011400	ORPHA:206443	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000505	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000618	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000712	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001250	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001251	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001260	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001337	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001350	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0001761	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002068	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002301	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002373	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0002445	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0003484	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0007018	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0008936	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0010830	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0011968	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0031006	ORPHA:206443	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206443	Late-infantile/juvenile Krabbe disease		HP:0000737	ORPHA:206443	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:660	Omphalocele		HP:0001539	ORPHA:660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:660	Omphalocele		HP:0001622	ORPHA:660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:660	Omphalocele		HP:0011432	ORPHA:660	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:660	Omphalocele		HP:0011425	ORPHA:660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:660	Omphalocele		HP:0002091	ORPHA:660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0000160	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0000233	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0000286	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0000343	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0000457	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0001539	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0002714	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1906	Fetal valproate spectrum disorder		HP:0003196	ORPHA:1906	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000750	ORPHA:353281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001249	ORPHA:353281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001999	ORPHA:353281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000028	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000079	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000189	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000444	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000708	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000712	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000722	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000733	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0012760	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000756	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001508	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001513	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001627	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002019	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002020	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002205	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002353	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002750	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002870	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0004322	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0005484	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0007086	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0009765	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0009834	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0009836	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0010055	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0011087	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0011304	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0025269	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0100710	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0100852	ORPHA:353281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000010	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000047	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000076	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000126	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000388	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000405	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000407	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000488	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000501	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000539	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000668	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000670	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000678	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000689	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000718	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000752	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000787	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000932	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001250	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001252	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001344	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001382	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001510	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001629	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001631	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001643	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002090	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002308	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002664	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002999	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0003319	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0005743	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0010562	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0010674	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0011069	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0031546	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0100716	ORPHA:353281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000518	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000589	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0000695	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001642	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001647	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001650	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0001680	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002099	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002341	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002566	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0002858	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0003396	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0005363	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0005374	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0010302	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0010775	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353281	Rubinstein-Taybi syndrome due to 16p13.3 microdeletion		HP:0030434	ORPHA:353281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000160	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000256	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000272	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000286	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000293	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000316	ORPHA:261295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000327	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000343	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000391	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000431	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000494	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0000768	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0001250	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0001252	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0001263	ORPHA:261295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0001631	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0001716	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0002119	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0004322	ORPHA:261295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0005280	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0008551	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0010059	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261295	20p12.3 microdeletion syndrome		HP:0011304	ORPHA:261295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324713	ABeta amyloidosis, Italian type		HP:0000726	ORPHA:324713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324713	ABeta amyloidosis, Italian type		HP:0001250	ORPHA:324713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324713	ABeta amyloidosis, Italian type		HP:0001259	ORPHA:324713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324713	ABeta amyloidosis, Italian type		HP:0001268	ORPHA:324713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324713	ABeta amyloidosis, Italian type		HP:0001297	ORPHA:324713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324713	ABeta amyloidosis, Italian type		HP:0001342	ORPHA:324713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324713	ABeta amyloidosis, Italian type		HP:0002076	ORPHA:324713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000252	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000276	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000316	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000426	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000494	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001249	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001251	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001263	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0002421	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0007447	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0008064	ORPHA:66631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000496	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000648	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001273	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001284	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001302	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0002126	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0003134	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0009830	ORPHA:66631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000093	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000100	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000135	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000164	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000268	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000400	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000407	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000457	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000478	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0000504	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001250	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001297	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0001635	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66631	CEDNIK syndrome		HP:0004322	ORPHA:66631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66630	Congenital pseudoarthrosis of the clavicle		HP:0000891	ORPHA:66630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66630	Congenital pseudoarthrosis of the clavicle		HP:0000924	ORPHA:66630	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66630	Congenital pseudoarthrosis of the clavicle		HP:0001651	ORPHA:66630	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66630	Congenital pseudoarthrosis of the clavicle		HP:0001696	ORPHA:66630	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66630	Congenital pseudoarthrosis of the clavicle		HP:0002758	ORPHA:66630	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66630	Congenital pseudoarthrosis of the clavicle		HP:0006585	ORPHA:66630	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0001347	ORPHA:320355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0002061	ORPHA:320355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0002064	ORPHA:320355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0002314	ORPHA:320355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0007020	ORPHA:320355	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0000012	ORPHA:320355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0003701	ORPHA:320355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0007210	ORPHA:320355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0030237	ORPHA:320355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41		HP:0100561	ORPHA:320355	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41	NOT	HP:0001250	ORPHA:320355	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41	NOT	HP:0002921	ORPHA:320355	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41	NOT	HP:0003457	ORPHA:320355	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:320355	Autosomal dominant spastic paraplegia type 41	NOT	HP:0012898	ORPHA:320355	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000113	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000126	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000154	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000158	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000160	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000175	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000202	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000218	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000238	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000252	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000272	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000280	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000316	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000319	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000347	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000365	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000369	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000445	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000448	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000470	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000486	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000494	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000508	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0000518	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001182	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001249	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001252	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001263	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001276	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001371	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001510	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001511	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001643	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001650	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0001883	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0002162	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0002230	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0002650	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0003202	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0004209	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0004322	ORPHA:261290	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0004383	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0005487	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0008661	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0008736	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0009890	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0009928	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0010481	ORPHA:261290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0011229	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261290	Trisomy 17p syndrome		HP:0012471	ORPHA:261290	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000160	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000175	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000218	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000233	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000248	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000252	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000276	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000324	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000343	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000347	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000348	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000369	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000426	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000444	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000463	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000486	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000494	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000677	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000678	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000717	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000718	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000739	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0000750	ORPHA:251019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0001166	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0001252	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0001263	ORPHA:251019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0001510	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0001762	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0001863	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0002213	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0002360	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0002546	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0004209	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0004322	ORPHA:251019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0001382	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0007018	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0008070	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0008734	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0010059	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0010864	ORPHA:251019	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0011304	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0011968	ORPHA:251019	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251019	2q32q33 deletion syndrome		HP:0100024	ORPHA:251019	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0100033	ORPHA:66624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0000712	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0000716	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0000737	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0000751	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0002072	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0002360	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0002376	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0007018	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0008770	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0010865	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0100710	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0100852	ORPHA:66624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0000756	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0000805	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0002039	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0002183	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0002312	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0002829	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0005366	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0025253	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0031468	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS		HP:0040183	ORPHA:66624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66624	PANDAS	NOT	HP:0100754	ORPHA:66624	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000248	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000316	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000337	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000528	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000582	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000618	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0005288	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0009891	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0011220	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0100729	ORPHA:66625	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000218	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000286	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000343	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000358	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000400	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000653	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000687	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0000691	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0001162	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0001249	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0002006	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0006315	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0008736	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0009912	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0012639	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0045075	ORPHA:66625	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66625	Cerebrooculonasal syndrome		HP:0010806	ORPHA:66625	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000218	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000273	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000316	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000347	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000369	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000494	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000750	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001999	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002553	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0005322	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0005484	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0006200	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0008897	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0010055	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0011304	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0012758	ORPHA:353284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000028	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000077	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000119	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000189	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000444	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000478	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000508	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000708	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000712	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000722	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000733	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0012760	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000756	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001508	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001513	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001627	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002019	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002205	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002870	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0004322	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0007086	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0008752	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0008872	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0009765	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0009834	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0009836	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0011087	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0025269	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0030680	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0100710	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0100852	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0410263	ORPHA:353284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000010	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000034	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000047	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000076	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000079	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000126	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000388	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000405	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000486	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000501	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000540	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000559	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000579	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000639	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000668	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000670	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000678	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000689	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000718	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000752	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000787	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000932	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001128	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001159	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001249	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001252	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001273	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001344	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001385	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001382	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001511	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001561	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001629	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001631	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001643	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001655	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002020	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002090	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002308	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002835	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002858	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002999	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0003319	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0005743	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0007099	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0010051	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0010442	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0010674	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0011069	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0011470	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0012448	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0030047	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0031251	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0031546	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0100716	ORPHA:353284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000407	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000518	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000589	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0000695	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001181	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001250	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001642	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001647	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001650	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0001680	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002099	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002341	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002353	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0002566	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0003396	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0005363	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0005374	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0010562	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0010775	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353284	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency		HP:0030434	ORPHA:353284	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0001513	ORPHA:66628	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0003292	ORPHA:66628	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0000771	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0000786	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0000815	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0000842	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0002591	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0032218	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0005419	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0008187	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0008214	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0008724	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0008734	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0040171	ORPHA:66628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0000831	ORPHA:66628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0002155	ORPHA:66628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0002788	ORPHA:66628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0004926	ORPHA:66628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0005616	ORPHA:66628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66628	Obesity due to congenital leptin deficiency		HP:0008245	ORPHA:66628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000510	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000556	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000773	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000774	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000886	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000887	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0001510	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0002867	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0004322	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0005257	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0006431	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0007663	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0008786	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0009824	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0045027	ORPHA:168549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000926	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0002643	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0002812	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0003411	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0005916	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0006589	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0006603	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0006712	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0008515	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0008812	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0011947	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0012774	ORPHA:168549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000508	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000518	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000613	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000639	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000646	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000648	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0000938	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0001216	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0001530	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0002650	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0002866	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0002943	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0003086	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0003180	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0003375	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0003521	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0007641	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0007769	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0008444	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168549	Axial spondylometaphyseal dysplasia		HP:0100864	ORPHA:168549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001249	ORPHA:251014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001263	ORPHA:251014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000252	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000343	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000347	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000369	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000414	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000470	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000494	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001156	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001182	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001250	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001252	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001595	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001770	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001800	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001852	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002002	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002463	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002714	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002750	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0003422	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0004209	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0004322	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0005487	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0005916	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0010059	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0012745	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0100490	ORPHA:251014	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000023	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000028	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000175	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000232	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000233	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000243	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000275	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000280	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000286	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000294	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000316	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000324	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000486	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000508	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000520	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000568	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000588	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000589	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000612	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000664	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0000864	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001629	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001631	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0001773	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002119	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002120	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002650	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002808	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002991	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0002992	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0004279	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0006101	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0040071	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251014	2q31.1 microdeletion syndrome		HP:0100257	ORPHA:251014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0002829	ORPHA:66627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0001369	ORPHA:66627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0001376	ORPHA:66627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0001386	ORPHA:66627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0001387	ORPHA:66627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0002797	ORPHA:66627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0002815	ORPHA:66627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0005261	ORPHA:66627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0000372	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0000405	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0001003	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0001004	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0001384	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0003019	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0003028	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0003043	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0009811	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0009911	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0031520	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0040090	ORPHA:66627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0000934	ORPHA:66627	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0005186	ORPHA:66627	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0005195	ORPHA:66627	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66627	Tenosynovial giant cell tumor		HP:0040161	ORPHA:66627	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000175	ORPHA:1915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000219	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000252	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000275	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000286	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000319	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000347	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000358	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000463	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000486	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000506	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000508	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000568	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000691	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000708	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0000776	ORPHA:1915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0001249	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0001263	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0001328	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0001387	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0001511	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0001631	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0002230	ORPHA:1915	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0003196	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0003422	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0004322	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0004422	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0007477	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0010978	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0100335	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0100543	ORPHA:1915	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1915	Fetal alcohol syndrome		HP:0100761	ORPHA:1915	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0001596	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0002797	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0002861	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0008069	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0011830	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0100526	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000970	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000982	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0001072	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0001231	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0007410	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0008070	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0010783	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0031013	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0031057	ORPHA:659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000164	ORPHA:659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000407	ORPHA:659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000668	ORPHA:659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000670	ORPHA:659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0200042	ORPHA:659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000157	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0000168	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:659	Mutilating palmoplantar keratoderma with periorificial keratotic plaques		HP:0001250	ORPHA:659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002493	ORPHA:206448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0034322	ORPHA:206448	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0001251	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0001257	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0001273	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002418	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002922	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0003202	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0003487	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0006801	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0007199	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0007305	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0007361	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0012379	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0031993	ORPHA:206448	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0000572	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0000726	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0001268	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0001288	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002062	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002312	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002344	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002353	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002359	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002650	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0003474	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0003484	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0004302	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0004466	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0007141	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0007340	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0009830	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0010830	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0011096	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0011441	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0031006	ORPHA:206448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0000020	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0001761	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002136	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002273	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002301	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002371	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0002492	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206448	Adult Krabbe disease		HP:0100639	ORPHA:206448	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000463	ORPHA:1914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0003196	ORPHA:1914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0005280	ORPHA:1914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0008420	ORPHA:1914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0010655	ORPHA:1914	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000470	ORPHA:1914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0001156	ORPHA:1914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0001249	ORPHA:1914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0001511	ORPHA:1914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0002093	ORPHA:1914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0009882	ORPHA:1914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000158	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000238	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000316	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000365	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000453	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000505	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000518	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000520	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0000648	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0001250	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0001252	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0002475	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0008056	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0008551	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1914	Vitamin K antagonist embryofetopathy		HP:0030680	ORPHA:1914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000175	ORPHA:66629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000252	ORPHA:66629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0001249	ORPHA:66629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0001328	ORPHA:66629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0002251	ORPHA:66629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0004322	ORPHA:66629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000508	ORPHA:66629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000612	ORPHA:66629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0001252	ORPHA:66629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000047	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000048	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000307	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000316	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000340	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000400	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0000431	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0001250	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0001302	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0002079	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0002119	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0002209	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0006101	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66629	Goldberg-Shprintzen megacolon syndrome		HP:0045075	ORPHA:66629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0000282	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0001025	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0001939	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002027	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0003401	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0005225	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0007514	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0011971	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0012027	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0012252	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0025349	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0040315	ORPHA:100050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002013	ORPHA:100050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002014	ORPHA:100050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002015	ORPHA:100050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002018	ORPHA:100050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002094	ORPHA:100050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0100755	ORPHA:100050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0000172	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0001609	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002098	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0002615	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0005348	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0005483	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0011855	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100050	Hereditary angioedema type 1		HP:0100736	ORPHA:100050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000047	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000062	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000218	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000248	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000252	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000286	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000347	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000369	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000396	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000486	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000508	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0000664	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0001249	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0001263	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0001511	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0001629	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0001631	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0001636	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0001669	ORPHA:1913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0002650	ORPHA:1913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0003196	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0005280	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0007598	ORPHA:1913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0011039	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0011220	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1913	Fetal trimethadione syndrome		HP:0011800	ORPHA:1913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000028	ORPHA:1912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000048	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000154	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000175	ORPHA:1912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000232	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000235	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000252	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000286	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000316	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000364	ORPHA:1912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000358	ORPHA:1912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000377	ORPHA:1912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000457	ORPHA:1912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000474	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000486	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0000508	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0001199	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0001263	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0001511	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0001626	ORPHA:1912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0001804	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0002162	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0002208	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0002664	ORPHA:1912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0003196	ORPHA:1912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0004322	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0006610	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0007477	ORPHA:1912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0009882	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1912	Fetal hydantoin syndrome		HP:0100790	ORPHA:1912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0000079	ORPHA:1911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0001276	ORPHA:1911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0001347	ORPHA:1911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0001626	ORPHA:1911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0002084	ORPHA:1911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0009882	ORPHA:1911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0011100	ORPHA:1911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1911	Cocaine embryofetopathy		HP:0100657	ORPHA:1911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:655	Nephronophthisis		HP:0000083	ORPHA:655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:655	Nephronophthisis		HP:0001903	ORPHA:655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:655	Nephronophthisis		HP:0007703	ORPHA:655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0002664	ORPHA:654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0002667	ORPHA:654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0031500	ORPHA:654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0002027	ORPHA:654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0005580	ORPHA:654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0012587	ORPHA:654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0000028	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0000047	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0000085	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0000086	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0000526	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0000822	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0001528	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0001824	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0001901	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0001903	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0001945	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0002716	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0002896	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0002907	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0003072	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0008330	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0012871	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0031105	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0033834	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0100526	ORPHA:654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:654	Nephroblastoma		HP:0002094	ORPHA:654	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1910	Fetal iodine syndrome		HP:0000407	ORPHA:1910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1910	Fetal iodine syndrome		HP:0000486	ORPHA:1910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1910	Fetal iodine syndrome		HP:0000639	ORPHA:1910	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1910	Fetal iodine syndrome		HP:0000821	ORPHA:1910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1910	Fetal iodine syndrome		HP:0001249	ORPHA:1910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1910	Fetal iodine syndrome		HP:0001264	ORPHA:1910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1910	Fetal iodine syndrome		HP:0004374	ORPHA:1910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0000093	ORPHA:656	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0000969	ORPHA:656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0000097	ORPHA:656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0003774	ORPHA:656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0012622	ORPHA:656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0100539	ORPHA:656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0000737	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0001945	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0001967	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0002027	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0002315	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0003073	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0011947	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0012579	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0031504	ORPHA:656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0000707	ORPHA:656	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:656	Hereditary steroid-resistant nephrotic syndrome		HP:0002586	ORPHA:656	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001257	ORPHA:496641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001324	ORPHA:496641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001510	ORPHA:496641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002079	ORPHA:496641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002120	ORPHA:496641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0003202	ORPHA:496641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000648	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001263	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001272	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001344	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002069	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002187	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002191	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002445	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002465	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002878	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0005484	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0006808	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0007179	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0008947	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0010818	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0011968	ORPHA:496641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000020	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000316	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000347	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000582	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000687	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001251	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001284	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001357	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001561	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002015	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002342	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002376	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002380	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002650	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002804	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0003084	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0003236	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0004887	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0011451	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0012450	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0045075	ORPHA:496641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000011	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000400	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000733	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000767	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0000768	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001007	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001332	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0001374	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002373	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002524	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0002607	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0006532	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496641	Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome		HP:0007002	ORPHA:496641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0000708	ORPHA:324703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0000726	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0001249	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0001259	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0001263	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0001297	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0001342	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0002076	ORPHA:324703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0003401	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0003474	ORPHA:324703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324703	ABetaL34V amyloidosis		HP:0100659	ORPHA:324703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0000708	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0000726	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0001288	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0001297	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0001336	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0001342	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0002015	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0002354	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324708	ABeta amyloidosis, Iowa type		HP:0100659	ORPHA:324708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0000319	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0000365	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0000518	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0000639	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0000717	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0000954	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001250	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001251	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001319	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001476	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001508	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001510	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001876	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0001883	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0002020	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0002119	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0002191	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0002240	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0002714	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0002719	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0002813	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0003139	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0004322	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0007272	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0008066	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0009909	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0010655	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0011968	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251009	Maternal uniparental disomy of chromosome 1 syndrome		HP:0100651	ORPHA:251009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42665	Tietz syndrome		HP:0000365	ORPHA:42665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42665	Tietz syndrome		HP:0000593	ORPHA:42665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42665	Tietz syndrome		HP:0001000	ORPHA:42665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42665	Tietz syndrome		HP:0001010	ORPHA:42665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42665	Tietz syndrome		HP:0002226	ORPHA:42665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42665	Tietz syndrome		HP:0005599	ORPHA:42665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0000252	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0000331	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0001028	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0001269	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0002170	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0003764	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0007359	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0011124	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0025167	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0100494	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0100699	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0004426	ORPHA:398189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0008066	ORPHA:398189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:3000019	ORPHA:398189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0000175	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0000204	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398189	Focal facial dermal dysplasia type IV		HP:0000238	ORPHA:398189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000093	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000105	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000486	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000529	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000613	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000682	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000793	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000822	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000823	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0000970	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0001250	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0001319	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0001336	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0001363	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0001513	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0002591	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0002757	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0003072	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0003138	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0004322	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0004802	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0007021	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0007272	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0007641	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0007754	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0008066	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0012444	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0012587	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251004	Paternal uniparental disomy of chromosome 1 syndrome		HP:0030612	ORPHA:251004	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002036	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002300	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002381	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002673	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002748	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002749	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002812	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002827	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0003010	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0003510	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0001382	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0005743	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0007392	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0010529	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0100633	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0100699	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0100790	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000023	ORPHA:1901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000278	ORPHA:1901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000286	ORPHA:1901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000347	ORPHA:1901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002650	ORPHA:1901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0005280	ORPHA:1901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0100541	ORPHA:1901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000938	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000939	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000963	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0000974	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0001001	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0001252	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0001367	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0001373	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0001385	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0001387	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1901	Dermatosparaxis Ehlers-Danlos syndrome		HP:0002020	ORPHA:1901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000938	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000939	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000974	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000978	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000987	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001030	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001252	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001319	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0005659	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001382	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0012379	ORPHA:1900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000482	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001075	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001324	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001373	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001519	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001762	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002761	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002827	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002943	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0032153	ORPHA:1900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000023	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000501	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000540	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000541	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000545	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000592	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000767	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001058	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001315	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001537	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001634	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001892	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002194	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002495	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002617	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002647	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002999	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0003199	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0003324	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0003458	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0003690	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0003835	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0004942	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0005294	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0008780	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0020152	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0025019	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0025513	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0030043	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0031158	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0100295	ORPHA:1900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000243	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000377	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0000486	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001635	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0001763	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002091	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002624	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002705	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0002987	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0003477	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0006532	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0031189	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0031629	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1900	Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency		HP:0045052	ORPHA:1900	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0040318	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0010472	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0032999	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0012379	ORPHA:95159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0007537	ORPHA:95159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0008066	ORPHA:95159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001030	ORPHA:95159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0040320	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001878	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0012804	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0100699	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0030756	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001790	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001072	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0000953	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001010	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0002219	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0003401	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0000989	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0000969	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001744	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001892	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0000618	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0100532	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0500046	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001096	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0000656	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0000938	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0001560	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0040322	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0200041	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0005406	ORPHA:95159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0011457	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0004552	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0002797	ORPHA:95159	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0000939	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95159	Hepatoerythropoietic porphyria		HP:0012132	ORPHA:95159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000962	ORPHA:28378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000982	ORPHA:28378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0001249	ORPHA:28378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0007957	ORPHA:28378	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000613	ORPHA:28378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000639	ORPHA:28378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000708	ORPHA:28378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000975	ORPHA:28378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0004337	ORPHA:28378	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000252	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000272	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0000572	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0001250	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0001251	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0001337	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0001597	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:28378	Tyrosinemia type 2		HP:0002167	ORPHA:28378	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0001319	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0002015	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0002486	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0003326	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0003552	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0004875	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0010548	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0011809	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0011968	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0012892	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0012899	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0012900	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0012901	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0012903	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0012904	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0031372	ORPHA:684	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0003458	ORPHA:684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0008153	ORPHA:684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:684	Paramyotonia congenita of Von Eulenburg		HP:0011042	ORPHA:684	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0000980	ORPHA:75563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0001324	ORPHA:75563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0001903	ORPHA:75563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0011031	ORPHA:75563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0012378	ORPHA:75563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0000953	ORPHA:75563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0001744	ORPHA:75563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0001952	ORPHA:75563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0002094	ORPHA:75563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75563	X-linked sideroblastic anemia		HP:0002910	ORPHA:75563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000605	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000623	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002015	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002172	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002317	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002527	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002529	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0012535	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0100710	ORPHA:683	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000505	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000511	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000514	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000643	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000712	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000716	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000737	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000741	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000750	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0001260	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0001332	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002067	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002120	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002171	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002200	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002321	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002354	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002381	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0100543	ORPHA:683	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000496	ORPHA:683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0000726	ORPHA:683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0001337	ORPHA:683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:683	Progressive supranuclear palsy		HP:0002063	ORPHA:683	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003701	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003789	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003803	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0008936	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003473	ORPHA:424107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0000508	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0001270	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0001284	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0001288	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0001508	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0002047	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0002058	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0002205	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0002650	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0002828	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003198	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003388	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003458	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0003691	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0011968	ORPHA:424107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0000602	ORPHA:424107	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset		HP:0002747	ORPHA:424107	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset	NOT	HP:0003201	ORPHA:424107	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset	NOT	HP:0003236	ORPHA:424107	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:424107	Congenital myopathy with myasthenic-like onset	NOT	HP:0040191	ORPHA:424107	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0000597	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0001276	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0001288	ORPHA:682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0001315	ORPHA:682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0001371	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0001522	ORPHA:682	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0001635	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002047	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002093	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002153	ORPHA:682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002380	ORPHA:682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002486	ORPHA:682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002607	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002900	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0002902	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003198	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003202	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003236	ORPHA:682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003326	ORPHA:682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003401	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003457	ORPHA:682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003712	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0003752	ORPHA:682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0007215	ORPHA:682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0008872	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0011675	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0100021	ORPHA:682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0100613	ORPHA:682	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:682	Hyperkalemic periodic paralysis		HP:0100749	ORPHA:682	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000049	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000160	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000252	ORPHA:261279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000272	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000286	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000316	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000365	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000389	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000411	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000414	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000486	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000498	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000527	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000687	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000708	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000750	ORPHA:261279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0000960	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001252	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001347	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001376	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001508	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001511	ORPHA:261279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001631	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001643	ORPHA:261279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001763	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0001852	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0002007	ORPHA:261279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0002020	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0002092	ORPHA:261279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0002094	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0002553	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0002650	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0002803	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0003065	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0003182	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0003279	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0004209	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0004322	ORPHA:261279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0005280	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0005930	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0007598	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0010511	ORPHA:261279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0011342	ORPHA:261279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0011343	ORPHA:261279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0011803	ORPHA:261279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261279	17q23.1q23.2 microdeletion syndrome		HP:0100807	ORPHA:261279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0008153	ORPHA:681	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0012726	ORPHA:681	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0003457	ORPHA:681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0003470	ORPHA:681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0003752	ORPHA:681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0004303	ORPHA:681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0008180	ORPHA:681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0012240	ORPHA:681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0001315	ORPHA:681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0009020	ORPHA:681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0011998	ORPHA:681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0002747	ORPHA:681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0003394	ORPHA:681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0003694	ORPHA:681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0011675	ORPHA:681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0012531	ORPHA:681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0012548	ORPHA:681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0002203	ORPHA:681	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0008256	ORPHA:681	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis		HP:0030196	ORPHA:681	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis	NOT	HP:0002486	ORPHA:681	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:681	Hypokalemic periodic paralysis	NOT	HP:0006670	ORPHA:681	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0000978	ORPHA:231401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0001744	ORPHA:231401	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0001873	ORPHA:231401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0001875	ORPHA:231401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0001892	ORPHA:231401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0001935	ORPHA:231401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0002094	ORPHA:231401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0002488	ORPHA:231401	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0002721	ORPHA:231401	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0002863	ORPHA:231401	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0011903	ORPHA:231401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231401	Alpha-thalassemia-myelodysplastic syndrome		HP:0012378	ORPHA:231401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0000175	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0000490	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0000501	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0000568	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0000664	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0000750	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0001249	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0001250	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0001561	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0001631	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0001770	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0002463	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0002539	ORPHA:261272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0002575	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0003468	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0006101	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261272	17q12 microduplication syndrome		HP:0100716	ORPHA:261272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0000369	ORPHA:398173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0001128	ORPHA:398173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0002055	ORPHA:398173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0009743	ORPHA:398173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0011336	ORPHA:398173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0045075	ORPHA:398173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0000385	ORPHA:398173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0000666	ORPHA:398173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0004554	ORPHA:398173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0007651	ORPHA:398173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0000377	ORPHA:398173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0000387	ORPHA:398173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398173	Focal facial dermal dysplasia type II		HP:0000394	ORPHA:398173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0001824	ORPHA:677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0002013	ORPHA:677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0002014	ORPHA:677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0002027	ORPHA:677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0003270	ORPHA:677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0005213	ORPHA:677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0011432	ORPHA:677	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0000952	ORPHA:677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:677	Pancreatoblastoma		HP:0002733	ORPHA:677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0001974	ORPHA:676	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0002027	ORPHA:676	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0011227	ORPHA:676	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0100027	ORPHA:676	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0012379	ORPHA:676	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0000819	ORPHA:676	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0000952	ORPHA:676	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0005213	ORPHA:676	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:676	Autosomal dominant hereditary chronic pancreatitis		HP:0030247	ORPHA:676	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0004334	ORPHA:679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0100585	ORPHA:679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0200034	ORPHA:679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0001824	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002017	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002027	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002239	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0005244	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0010547	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0012378	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0031368	ORPHA:679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0000508	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0000518	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0000587	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0000651	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0001250	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0001637	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0001658	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0001697	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002076	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002140	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002202	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002321	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002586	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0002878	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0004420	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0006824	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0007021	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0009830	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0010936	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0012089	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0100576	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0100749	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:679	Malignant atrophic papulosis		HP:0100819	ORPHA:679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0000164	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0000166	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0000230	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0000704	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0000972	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0000982	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0000998	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0001053	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0001073	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0001166	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0001231	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0001581	ORPHA:678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0001597	ORPHA:678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0002205	ORPHA:678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0002230	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0002231	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0002514	ORPHA:678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0002797	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0002860	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0002861	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0006308	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0006323	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0008069	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0008404	ORPHA:678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0009804	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0011132	ORPHA:678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0100523	ORPHA:678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0100838	ORPHA:678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:678	Papillon-Lefèvre syndrome		HP:0200039	ORPHA:678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0000112	ORPHA:100024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0000939	ORPHA:100024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0001744	ORPHA:100024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0001824	ORPHA:100024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0001903	ORPHA:100024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0001945	ORPHA:100024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0002240	ORPHA:100024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0002716	ORPHA:100024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0002797	ORPHA:100024	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0005561	ORPHA:100024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0010702	ORPHA:100024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0010975	ORPHA:100024	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100024	Mu-heavy chain disease		HP:0030156	ORPHA:100024	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002024	ORPHA:100025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002244	ORPHA:100025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002961	ORPHA:100025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0001903	ORPHA:100025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002027	ORPHA:100025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002721	ORPHA:100025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002901	ORPHA:100025	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0001510	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0001541	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0001596	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0001744	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0001945	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002240	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002665	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100025	Alpha-heavy chain disease		HP:0002716	ORPHA:100025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0000830	ORPHA:631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0001510	ORPHA:631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0002750	ORPHA:631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0004322	ORPHA:631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0000295	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0000823	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0000824	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0001620	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0001998	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0003199	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0005280	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0006579	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0008070	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0011220	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0012743	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0030353	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0100678	ORPHA:631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0002857	ORPHA:631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:631	Non-acquired isolated growth hormone deficiency		HP:0030260	ORPHA:631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0000174	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0000988	ORPHA:100026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0001370	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0001744	ORPHA:100026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0001873	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0001890	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0001903	ORPHA:100026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0001945	ORPHA:100026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0001973	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0002015	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0002205	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0002240	ORPHA:100026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0002716	ORPHA:100026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0002797	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0002960	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0004332	ORPHA:100026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0005561	ORPHA:100026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0009830	ORPHA:100026	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0012378	ORPHA:100026	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100026	Gamma-heavy chain disease		HP:0100648	ORPHA:100026	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0012090	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0025439	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0100539	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0000024	ORPHA:449432	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0025426	ORPHA:449432	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0002960	ORPHA:449432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0003237	ORPHA:449432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0010287	ORPHA:449432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0032300	ORPHA:449432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0000217	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0001880	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0002716	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0003212	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0004431	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0007734	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0010286	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0010702	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0031281	ORPHA:449432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0000077	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0000083	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0000282	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0000820	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0005200	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0011801	ORPHA:449432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449432	IgG4-related submandibular gland disease		HP:0030151	ORPHA:449432	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000003	ORPHA:261265	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000028	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000049	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000070	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000083	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000239	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000365	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000717	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0000819	ORPHA:261265	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0001249	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0001250	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0001263	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0001562	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0002059	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0002463	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0002910	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0004322	ORPHA:261265	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0008678	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0011968	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0012157	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261265	17q12 microdeletion syndrome		HP:0100801	ORPHA:261265	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0001744	ORPHA:66661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0001824	ORPHA:66661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0002240	ORPHA:66661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0002716	ORPHA:66661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0012378	ORPHA:66661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0100242	ORPHA:66661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0100495	ORPHA:66661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0100720	ORPHA:66661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66661	Mast cell sarcoma		HP:0100721	ORPHA:66661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0002091	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0002151	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0003200	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0003546	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0003722	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0004322	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0008180	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0008994	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0009053	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0012240	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0030319	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0040014	ORPHA:457050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457050	Autosomal dominant mitochondrial myopathy with exercise intolerance		HP:0008997	ORPHA:457050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001627	ORPHA:216694	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001629	ORPHA:216694	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001702	ORPHA:216694	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0006705	ORPHA:216694	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011103	ORPHA:216694	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011553	ORPHA:216694	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001631	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001642	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001662	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0005150	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011539	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011552	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0030148	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0031546	ORPHA:216694	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0000961	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001508	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001635	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001643	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001651	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001659	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001696	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001709	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001716	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0001750	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0003388	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0004755	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0004935	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0005180	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0005185	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0006699	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0010316	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011538	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011581	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011590	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011621	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011663	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011667	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011675	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011682	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011688	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011704	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011705	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011707	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0012537	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0012722	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0031567	ORPHA:216694	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0004749	ORPHA:216694	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0004756	ORPHA:216694	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:216694	Congenitally corrected transposition of the great arteries		HP:0011599	ORPHA:216694	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0012534	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0031249	ORPHA:353253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0010829	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0010824	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0007377	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0032143	ORPHA:353253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0000223	ORPHA:353253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0000739	ORPHA:353253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0000716	ORPHA:353253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0030811	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0000168	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0000217	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0002315	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0002360	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0000712	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0031042	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353253	Burning mouth syndrome		HP:0010298	ORPHA:353253	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0001000	ORPHA:626	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0003764	ORPHA:626	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0005600	ORPHA:626	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0000958	ORPHA:626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0000970	ORPHA:626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0001058	ORPHA:626	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0000238	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0000708	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0000989	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0000998	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0001053	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0001250	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0001482	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0002176	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0002315	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0002516	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0012056	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0012758	ORPHA:626	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0000028	ORPHA:626	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0004912	ORPHA:626	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:626	Large/giant congenital melanocytic nevus		HP:0010314	ORPHA:626	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000518	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000952	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001249	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001250	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001263	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001433	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0003575	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0004446	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0005525	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0008897	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0011972	ORPHA:168577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000252	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000256	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000400	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000470	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000475	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0000639	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001156	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001251	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001258	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001276	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0001334	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0002719	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0002908	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0004322	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0007229	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0010306	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0010920	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0012430	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0012448	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0012695	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168577	Hereditary cryohydrocytosis with reduced stomatin		HP:0100022	ORPHA:168577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000256	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000772	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000889	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000944	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001511	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002650	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002983	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0003312	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0004322	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0005280	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0005916	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0005930	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0006487	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0008434	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0008921	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0009381	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0009623	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0009748	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0009773	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0011001	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0011800	ORPHA:628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000175	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000293	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000316	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000358	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000396	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000430	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000592	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001234	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001252	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001373	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001385	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001387	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001762	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001852	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002093	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002205	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002808	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002857	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002938	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002947	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0005619	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0005857	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0009465	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0034392	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0100490	ORPHA:628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000028	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000160	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000337	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000347	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000365	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000402	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000460	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000494	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0000974	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001156	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002176	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0002514	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0003042	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0004209	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0001382	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0006536	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0009890	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:628	Diastrophic dysplasia		HP:0100761	ORPHA:628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0000100	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0000821	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0000944	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0000958	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0000969	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0000989	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001019	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001072	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001508	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001596	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001744	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001831	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001880	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001903	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001945	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0001974	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0002028	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0002090	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0002240	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0002665	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0002716	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0002960	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0004332	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0004430	ORPHA:39041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0007549	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0100646	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0100806	ORPHA:39041	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39041	Omenn syndrome		HP:0100840	ORPHA:39041	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000164	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000276	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000303	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000411	ORPHA:627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000426	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000448	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000482	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000486	ORPHA:627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000501	ORPHA:627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000505	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000518	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000541	ORPHA:627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000568	ORPHA:627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000572	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000639	ORPHA:627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0000708	ORPHA:627	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0001249	ORPHA:627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0010049	ORPHA:627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:627	Nance-Horan syndrome		HP:0011069	ORPHA:627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0000505	ORPHA:622	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0000639	ORPHA:622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0000709	ORPHA:622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0000726	ORPHA:622	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0001250	ORPHA:622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0001251	ORPHA:622	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0001252	ORPHA:622	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0001254	ORPHA:622	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0001263	ORPHA:622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0001508	ORPHA:622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0001980	ORPHA:622	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0002013	ORPHA:622	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:622	Homocystinuria without methylmalonic aciduria		HP:0002120	ORPHA:622	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001324	ORPHA:168572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002058	ORPHA:168572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000028	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000175	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001252	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001270	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001488	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001762	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002020	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002047	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002093	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002803	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002804	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0003202	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0004322	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0008458	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0010674	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0011968	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0012084	ORPHA:168572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000193	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000218	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000347	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000405	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000494	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001260	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001315	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002714	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0011819	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0100295	ORPHA:168572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0000329	ORPHA:168572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001256	ORPHA:168572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0001382	ORPHA:168572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0002540	ORPHA:168572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168572	Native American myopathy		HP:0012385	ORPHA:168572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0000572	ORPHA:39044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0001098	ORPHA:39044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0012054	ORPHA:39044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0000541	ORPHA:39044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0011524	ORPHA:39044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0012055	ORPHA:39044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0000539	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0007902	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0007906	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0008494	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0010920	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0011499	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0012508	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0030786	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0030800	ORPHA:39044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0100533	ORPHA:39044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39044	Uveal melanoma		HP:0200026	ORPHA:39044	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0000643	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0001304	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0001336	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002067	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002072	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002172	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002322	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002362	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002378	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002548	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0004373	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0007158	ORPHA:53351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0001288	ORPHA:53351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002359	ORPHA:53351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0002451	ORPHA:53351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0006511	ORPHA:53351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0010808	ORPHA:53351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0011951	ORPHA:53351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53351	X-linked dystonia-parkinsonism		HP:0031162	ORPHA:53351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0000961	ORPHA:621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0012119	ORPHA:621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0000707	ORPHA:621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0001597	ORPHA:621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0002875	ORPHA:621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0025118	ORPHA:621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0000252	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0000565	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0000592	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0001257	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0001263	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0001272	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0002283	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0002305	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0002451	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0002510	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0006808	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0006913	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0007112	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0010864	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0011344	ORPHA:621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0001250	ORPHA:621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0001276	ORPHA:621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0001518	ORPHA:621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0012448	ORPHA:621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:621	Hereditary methemoglobinemia		HP:0012697	ORPHA:621	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0000501	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0000969	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0001034	ORPHA:624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0001052	ORPHA:624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0001249	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0001250	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0001269	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0001291	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0002170	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0002204	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0002301	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0002514	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0002650	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0002814	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0002817	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0004936	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0005293	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0007400	ORPHA:624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0011675	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0100026	ORPHA:624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0100559	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0200034	ORPHA:624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:624	Familial multiple nevi flammei		HP:0200042	ORPHA:624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000054	ORPHA:52022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000248	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000286	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000322	ORPHA:52022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000347	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000426	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000430	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000437	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000455	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000486	ORPHA:52022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000639	ORPHA:52022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000821	ORPHA:52022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000822	ORPHA:52022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0000823	ORPHA:52022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0001249	ORPHA:52022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0001250	ORPHA:52022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0001263	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0001903	ORPHA:52022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0002667	ORPHA:52022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0002697	ORPHA:52022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0002714	ORPHA:52022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0004331	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52022	Potocki-Shaffer syndrome		HP:0100777	ORPHA:52022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0001249	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0001258	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0002061	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0002064	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0003487	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0005830	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0006380	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0006466	ORPHA:320396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0001263	ORPHA:320396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0001270	ORPHA:320396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0001347	ORPHA:320396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0012043	ORPHA:320396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0000545	ORPHA:320396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320396	Autosomal recessive spastic paraplegia type 45		HP:0000648	ORPHA:320396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000348	ORPHA:261250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000411	ORPHA:261250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000717	ORPHA:261250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000154	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000218	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000307	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000319	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000343	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000347	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000609	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0001250	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002007	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002079	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002119	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002342	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0007165	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0030048	ORPHA:261250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000028	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000276	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000325	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000365	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000384	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000389	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000463	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000483	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000486	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000505	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000545	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000582	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000639	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0000750	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0001385	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0001629	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0001644	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0001653	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0001873	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002015	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002553	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002650	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0002808	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0004422	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0005518	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0006315	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0009623	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0010720	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0011968	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261250	16q24.3 microdeletion syndrome		HP:0012471	ORPHA:261250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000316	ORPHA:398156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000456	ORPHA:398156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000160	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000252	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000289	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000324	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000347	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000384	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000405	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000430	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000445	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000636	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0001140	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0001629	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0002084	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0002650	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0006931	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0008551	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0010609	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0410030	ORPHA:398156	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000175	ORPHA:398156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398156	Oculoauriculofrontonasal syndrome		HP:0000256	ORPHA:398156	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0000488	ORPHA:618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0000958	ORPHA:618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0001480	ORPHA:618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0001595	ORPHA:618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0002071	ORPHA:618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0002861	ORPHA:618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0002894	ORPHA:618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0003764	ORPHA:618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0006753	ORPHA:618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0100013	ORPHA:618	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:618	Familial melanoma		HP:0100763	ORPHA:618	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0000518	ORPHA:320391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0001251	ORPHA:320391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002061	ORPHA:320391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0001288	ORPHA:320391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0003487	ORPHA:320391	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0001272	ORPHA:320391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002059	ORPHA:320391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002120	ORPHA:320391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002500	ORPHA:320391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0007371	ORPHA:320391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0100543	ORPHA:320391	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0000020	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0000365	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0000639	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0000726	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0000789	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0001347	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0001761	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002078	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002136	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002346	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002464	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0002650	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0003477	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0006938	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0006986	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0007256	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0008003	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0008734	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0012207	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0012864	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0012865	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320391	Autosomal recessive spastic paraplegia type 46		HP:0100261	ORPHA:320391	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0011672	ORPHA:615	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0006691	ORPHA:615	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0030148	ORPHA:615	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0002875	ORPHA:615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0003388	ORPHA:615	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0000952	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0001396	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0001541	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0001635	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0001640	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0001907	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0001945	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0005180	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0006689	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0010741	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0100749	ORPHA:615	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0002617	ORPHA:615	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:615	Familial atrial myxoma		HP:0004944	ORPHA:615	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0002486	ORPHA:614	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0003457	ORPHA:614	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0003552	ORPHA:614	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0003740	ORPHA:614	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0100284	ORPHA:614	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0003326	ORPHA:614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0003712	ORPHA:614	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0002312	ORPHA:614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0003394	ORPHA:614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0003458	ORPHA:614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0008872	ORPHA:614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0009063	ORPHA:614	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0002015	ORPHA:614	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0011675	ORPHA:614	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:614	Thomsen and Becker disease		HP:0031546	ORPHA:614	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0000010	ORPHA:617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0000036	ORPHA:617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0000076	ORPHA:617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0000126	ORPHA:617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0000787	ORPHA:617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0001945	ORPHA:617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0002027	ORPHA:617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0002907	ORPHA:617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0008676	ORPHA:617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:617	Congenital primary megaureter		HP:0010935	ORPHA:617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002885	ORPHA:616	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0000270	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0001251	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0001254	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0001291	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0001310	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002017	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002073	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002080	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002315	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002516	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0004481	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0007129	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0009878	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0012658	ORPHA:616	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0000238	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0000529	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0000651	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0000737	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0001263	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002321	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002350	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0003418	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0005227	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0005561	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0007352	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0007824	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0008619	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0010302	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0011695	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0100543	ORPHA:616	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0002910	ORPHA:616	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0003006	ORPHA:616	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:616	Medulloblastoma		HP:0100526	ORPHA:616	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0002960	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003200	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003202	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003236	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003457	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003701	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003731	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003805	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0004303	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0009071	ORPHA:611	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0001315	ORPHA:611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0008872	ORPHA:611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0034153	ORPHA:611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:611	Inclusion body myositis		HP:0003326	ORPHA:611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001324	ORPHA:610	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001371	ORPHA:610	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003458	ORPHA:610	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003560	ORPHA:610	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0009073	ORPHA:610	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0030095	ORPHA:610	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0000467	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001220	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001239	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001288	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001288	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002460	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002828	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003236	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003325	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003731	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0006466	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0009058	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0100490	ORPHA:610	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0000962	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001073	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001382	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0001771	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002086	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002515	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002650	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002791	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002938	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0002987	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003306	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003327	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003391	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003691	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003700	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0003805	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0009027	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0010176	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0012497	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:610	Bethlem muscular dystrophy		HP:0032152	ORPHA:610	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0002155	ORPHA:650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0003233	ORPHA:650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0031799	ORPHA:650	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0000083	ORPHA:650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0000093	ORPHA:650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0001878	ORPHA:650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0002621	ORPHA:650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0007957	ORPHA:650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0012213	ORPHA:650	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0000505	ORPHA:650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0001919	ORPHA:650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0003774	ORPHA:650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:650	LCAT deficiency		HP:0005181	ORPHA:650	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002865	ORPHA:653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0000739	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0000975	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0000980	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0001962	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002014	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002315	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002640	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002666	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003345	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003528	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003639	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0008208	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0011781	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0011976	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0011978	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0025388	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0032241	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0100735	ORPHA:653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0000787	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0001324	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0001519	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002019	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002150	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002251	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002751	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002864	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002896	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0002897	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003072	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003165	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003270	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003307	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0008200	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0010622	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0010726	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0012471	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0025151	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0025289	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0030430	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0030809	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0030833	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0031023	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0032346	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0100526	ORPHA:653	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0001382	ORPHA:653	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0003758	ORPHA:653	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:653	Multiple endocrine neoplasia type 2		HP:0007126	ORPHA:653	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0003072	ORPHA:652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0008200	ORPHA:652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0008208	ORPHA:652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0010615	ORPHA:652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0031058	ORPHA:652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000802	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000849	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001012	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001824	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002014	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002020	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002027	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002044	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002150	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002893	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002894	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0004349	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0004398	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0005605	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0006767	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0040306	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0100829	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0500167	ORPHA:652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000141	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000169	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000716	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000736	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000787	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000822	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000845	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0000853	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001254	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001289	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001293	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001579	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001944	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002013	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002018	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002019	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002039	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002248	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002249	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002315	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002588	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002659	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002797	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002858	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002890	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0003118	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0006723	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0006744	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0007449	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0011407	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0011760	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0012197	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0012232	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0030405	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0032044	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0040085	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0100570	ORPHA:652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0001259	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002666	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0002888	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0003144	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0003528	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0006780	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0008291	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0011151	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0011759	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0011761	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0011762	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0030404	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0030445	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:652	Multiple endocrine neoplasia type 1		HP:0100522	ORPHA:652	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0012379	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0030272	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0003281	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0012465	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0031876	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0032500	ORPHA:101330	TAS		HP:0040281			M	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0030955	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0200123	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0002725	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0003774	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0000819	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0001397	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0004377	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0000992	ORPHA:101330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0008066	ORPHA:101330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0001030	ORPHA:101330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0040189	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0001058	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0012531	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0005406	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0031292	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0000998	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0001010	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0000953	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0001007	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0100699	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0000559	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0000656	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0002910	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0001405	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0033197	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0033196	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0001402	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0010473	ORPHA:101330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0010472	ORPHA:101330	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0032999	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0012217	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0003452	ORPHA:101330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101330	Porphyria cutanea tarda		HP:0006562	ORPHA:101330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0002205	ORPHA:320385	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000248	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000252	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000293	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000294	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000311	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000338	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000470	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000475	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0000678	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001249	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001260	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001263	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001284	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001290	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001310	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0002066	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0004322	ORPHA:320385	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001250	ORPHA:320385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0001272	ORPHA:320385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0002059	ORPHA:320385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0002079	ORPHA:320385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320385	Hereditary sensory and autonomic neuropathy due to TECPR2 mutation		HP:0002871	ORPHA:320385	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0000268	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0000717	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0000718	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0000767	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001161	ORPHA:261243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001166	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001249	ORPHA:261243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001263	ORPHA:261243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001363	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001629	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001631	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001636	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001669	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001680	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001763	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0002463	ORPHA:261243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0001382	ORPHA:261243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0007018	ORPHA:261243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261243	16p13.11 microduplication syndrome		HP:0100753	ORPHA:261243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0000708	ORPHA:100006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0000726	ORPHA:100006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0001250	ORPHA:100006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0001268	ORPHA:100006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0001297	ORPHA:100006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0001342	ORPHA:100006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0002315	ORPHA:100006	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0002514	ORPHA:100006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0011970	ORPHA:100006	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100006	ABeta amyloidosis, Dutch type		HP:0100613	ORPHA:100006	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:100008	ACys amyloidosis		HP:0001297	ORPHA:100008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100008	ACys amyloidosis		HP:0001342	ORPHA:100008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100008	ACys amyloidosis		HP:0011034	ORPHA:100008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100008	ACys amyloidosis		HP:0011970	ORPHA:100008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100008	ACys amyloidosis		HP:0100613	ORPHA:100008	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:66633	Sensorineural hearing loss-early graying-essential tremor syndrome		HP:0000407	ORPHA:66633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66633	Sensorineural hearing loss-early graying-essential tremor syndrome		HP:0000592	ORPHA:66633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66633	Sensorineural hearing loss-early graying-essential tremor syndrome		HP:0001100	ORPHA:66633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66633	Sensorineural hearing loss-early graying-essential tremor syndrome		HP:0001337	ORPHA:66633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66633	Sensorineural hearing loss-early graying-essential tremor syndrome		HP:0002216	ORPHA:66633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000218	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000273	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000316	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000347	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000369	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000494	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000750	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001249	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001999	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002553	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0005322	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0005484	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0006200	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0008897	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0010055	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0011304	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0012758	ORPHA:353277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000028	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000077	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000119	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000189	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000444	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000478	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000508	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000708	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000712	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000722	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000733	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0012760	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000756	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001508	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001513	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001627	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002019	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002205	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002870	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0004322	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0007086	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0008752	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0008872	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0009765	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0009834	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0009836	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0011087	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0025269	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0030680	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0100710	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0100852	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0410263	ORPHA:353277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000010	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000034	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000047	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000076	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000079	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000126	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000388	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000405	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000486	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000501	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000540	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000559	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000579	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000639	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000668	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000670	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000678	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000689	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000718	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000752	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000787	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000932	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001128	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001159	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001181	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001252	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001273	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001344	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001385	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001382	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001511	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001561	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001629	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001631	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001643	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001655	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002020	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002090	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002308	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002835	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002858	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002999	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0003319	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0005743	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0007099	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0010051	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0010442	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0010674	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0011069	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0011470	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0012448	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0030047	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0031251	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0031546	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0100716	ORPHA:353277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000407	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000518	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000589	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0000695	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001250	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001642	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001647	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001650	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0001680	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002099	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002341	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002353	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0002566	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0003396	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0005363	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0005374	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0010562	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0010775	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:353277	Rubinstein-Taybi syndrome due to CREBBP mutations		HP:0030434	ORPHA:353277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0000496	ORPHA:293168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0001257	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0001258	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0001260	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0001347	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0002193	ORPHA:293168	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0002425	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0002445	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0002510	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0005216	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293168	Infantile-onset ascending hereditary spastic paralysis		HP:0007256	ORPHA:293168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001251	ORPHA:66634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001510	ORPHA:66634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001644	ORPHA:66634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0003530	ORPHA:66634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0003535	ORPHA:66634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001511	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001657	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0002151	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0002194	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0002910	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0004840	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0004856	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0012758	ORPHA:66634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0000051	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0000648	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001250	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001414	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001998	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0008689	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0008736	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0011623	ORPHA:66634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0000821	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001319	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001324	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001332	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0001999	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0002061	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0002345	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0002376	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0003700	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0007146	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0007366	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0008619	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0008762	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0009110	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0100660	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66634	Dilated cardiomyopathy with ataxia		HP:0100702	ORPHA:66634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0000175	ORPHA:66637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0000470	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0000921	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0002098	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0002475	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0003275	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0004599	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0005562	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0005640	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0010306	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:66637	Diaphanospondylodysostosis		HP:0100625	ORPHA:66637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000028	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000033	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000037	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000127	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000144	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000151	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000771	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000823	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000848	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000939	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0001197	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0001274	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0001508	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0001941	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0001944	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0001998	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0002013	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0002153	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0002615	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0002750	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0002902	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0003107	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0003154	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0004319	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0004349	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0007440	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0007574	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008073	ORPHA:168558	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008163	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008187	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008207	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008730	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008734	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0010789	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0011106	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0011749	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0011968	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0012244	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0012245	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0012598	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0012605	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0030349	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0030369	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0100779	ORPHA:168558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000835	ORPHA:168558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0001622	ORPHA:168558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008232	ORPHA:168558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0011969	ORPHA:168558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0000142	ORPHA:168558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0008665	ORPHA:168558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168558	46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency		HP:0012854	ORPHA:168558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0000271	ORPHA:398147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0012532	ORPHA:398147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0025282	ORPHA:398147	TAS		HP:0040282			M	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0000716	ORPHA:398147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0000739	ORPHA:398147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0003401	ORPHA:398147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0003489	ORPHA:398147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0007328	ORPHA:398147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0032143	ORPHA:398147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain		HP:0003474	ORPHA:398147	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:398147	Persistent idiopathic facial pain	NOT	HP:0012639	ORPHA:398147	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0001249	ORPHA:320380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0001258	ORPHA:320380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0001263	ORPHA:320380	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0000486	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0001260	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0001288	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0002015	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0002064	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0002079	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0007766	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0008366	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0030891	ORPHA:320380	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0000218	ORPHA:320380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0004322	ORPHA:320380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0006970	ORPHA:320380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320380	Autosomal recessive spastic paraplegia type 54		HP:0030051	ORPHA:320380	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0003115	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0004322	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0004415	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001382	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0006610	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0010318	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0011800	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0030680	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0100625	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000028	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000078	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000486	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000635	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001252	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001641	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001743	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001892	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001928	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0002162	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0002208	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0002240	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0002650	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0002750	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0007477	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0008872	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0011362	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0011675	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0011869	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0012758	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0100763	ORPHA:648	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000407	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000639	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000938	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000978	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000995	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001004	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001156	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001249	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001328	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001631	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001639	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001680	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0002974	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0004209	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0008897	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0010946	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0011381	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0012209	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0012569	ORPHA:648	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001643	ORPHA:648	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000044	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000179	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000218	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000316	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000325	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000347	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000348	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000358	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000391	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000465	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000474	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000476	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000494	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000508	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000520	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000767	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0000768	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001260	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0001324	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:648	Noonan syndrome		HP:0002167	ORPHA:648	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000175	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000252	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000271	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000278	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000294	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000340	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000364	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000400	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000426	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000444	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000448	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000470	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000492	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000582	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0000992	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0001268	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0001324	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0001480	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0001595	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0001873	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0001878	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0001890	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002002	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002023	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002025	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002028	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002205	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002269	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002488	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002664	ORPHA:647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002665	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002859	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0002878	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0003011	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0003202	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0003220	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0004322	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0004326	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0005280	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0005425	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0006532	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0007018	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0009733	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0011362	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0012190	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0012191	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0012732	ORPHA:647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0100335	ORPHA:647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:647	Nijmegen breakage syndrome		HP:0100515	ORPHA:647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0000926	ORPHA:168555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0001376	ORPHA:168555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0002657	ORPHA:168555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0002812	ORPHA:168555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0002983	ORPHA:168555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0003510	ORPHA:168555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0004279	ORPHA:168555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168555	Spondylometaphyseal dysplasia, A4 type		HP:0006603	ORPHA:168555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0100963	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000467	ORPHA:206436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001053	ORPHA:206436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001264	ORPHA:206436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001601	ORPHA:206436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0010729	ORPHA:206436	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0031161	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000238	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000365	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000572	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000613	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000618	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000648	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001250	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001263	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001265	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001298	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001324	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001336	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001347	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001824	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002013	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002020	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002098	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002123	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002179	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002421	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002506	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000649	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000737	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001257	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001268	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001955	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002344	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002922	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0004302	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0007141	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0012379	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0030215	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0033031	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0034322	ORPHA:206436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0000762	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001188	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0001508	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002061	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002361	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002518	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0004466	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0008936	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0009830	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0011968	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0012706	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0012708	ORPHA:206436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002516	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002719	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0002878	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0003394	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0003547	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0003552	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0004326	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0005968	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0007103	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0011444	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0011448	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0011470	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0025013	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0030211	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0031860	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0040194	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:206436	Infantile Krabbe disease		HP:0040195	ORPHA:206436	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000028	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000233	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000252	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000272	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000375	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000400	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000407	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000411	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000446	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000490	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000501	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000518	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000532	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000541	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000568	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000601	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000615	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000618	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000639	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000647	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000648	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000708	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000709	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000717	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000733	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000737	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000738	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000739	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000819	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0000823	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001083	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001250	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001252	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001276	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001324	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001347	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001508	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0002076	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0002120	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0002169	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0002353	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0002360	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0002376	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0002650	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0004326	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0004327	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0005293	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0001249	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0007018	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0007360	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0007676	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0007833	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0007957	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0007968	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0008046	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0008063	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0010662	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0010978	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0011039	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0100012	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0100639	ORPHA:649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0100716	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0100718	ORPHA:649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:649	Norrie disease		HP:0100742	ORPHA:649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000365	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000510	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000543	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000618	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000639	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000726	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000737	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0000763	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0001133	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0001136	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0001250	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0001251	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0001263	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0002119	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0002120	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0002315	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0003394	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0003487	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0003701	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0003739	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0004322	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0007117	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0007240	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0007814	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0010864	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0012751	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome		HP:0030588	ORPHA:644	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:644	NARP syndrome	NOT	HP:0008316	ORPHA:644	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001284	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001290	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001382	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002235	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001288	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0003405	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0003429	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0003701	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0005109	ORPHA:643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001249	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001257	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001317	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001761	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0001762	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002224	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002317	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002460	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002650	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002936	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0005922	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0010628	ORPHA:643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002527	ORPHA:643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0002857	ORPHA:643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0003487	ORPHA:643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0003690	ORPHA:643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:643	Giant axonal neuropathy		HP:0012503	ORPHA:643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000511	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000708	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000952	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001268	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001288	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001392	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002015	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002240	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002344	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0003349	ORPHA:646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000365	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001250	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001251	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001260	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001332	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001618	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001744	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002167	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002451	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002530	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0003651	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0004333	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0007240	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0010318	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0011446	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0011968	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0100022	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0100543	ORPHA:646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000709	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000716	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000718	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000722	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000726	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000734	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000741	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000744	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0000750	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001249	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001252	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001263	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001328	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001336	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001337	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001433	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002059	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002061	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002072	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002079	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002080	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002197	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002312	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002359	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002360	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002367	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002376	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002415	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002493	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002524	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0006855	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0007256	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0007359	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0008765	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0011098	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0011400	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0011471	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0012433	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0030050	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0100753	ORPHA:646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001399	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001541	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001789	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0001791	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002088	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002093	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002113	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002133	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0002878	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0006913	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0007108	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0007302	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:646	Niemann-Pick disease type C		HP:0011951	ORPHA:646	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0003431	ORPHA:640	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0009830	ORPHA:640	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0001324	ORPHA:640	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0002650	ORPHA:640	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0003401	ORPHA:640	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0007141	ORPHA:640	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0200101	ORPHA:640	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0000407	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0001265	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0001605	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0001608	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0001761	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0002093	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0003394	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0003693	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0003704	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0003738	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:640	Hereditary neuropathy with liability to pressure palsies		HP:0006824	ORPHA:640	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0010617	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0010618	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0011330	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0011968	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000238	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000343	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000494	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000684	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0001250	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0002119	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0002308	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0002808	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0003196	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0005616	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0001382	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0009894	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0010442	ORPHA:77301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000098	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000160	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000202	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000243	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000256	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000286	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000369	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000470	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000486	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000488	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000518	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000568	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000752	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000767	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000772	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0000925	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0001249	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0001252	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0001263	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0001520	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0001537	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0002671	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0002885	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0005462	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0010603	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0010610	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0010612	ORPHA:77301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0002667	ORPHA:77301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77301	Monosomy 9q22.3 syndrome		HP:0002859	ORPHA:77301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0002002	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0002566	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0002808	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0007894	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0010880	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0100277	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000202	ORPHA:77300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0011340	ORPHA:77300	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000252	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000347	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000369	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000377	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000430	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000431	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000457	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000545	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000572	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000587	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000639	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000767	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0000891	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77300	Auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome		HP:0001357	ORPHA:77300	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000742	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000970	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001249	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002726	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002754	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0003134	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0007021	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0010829	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0011136	ORPHA:642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000958	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000987	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001328	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001954	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001288	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002661	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002821	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0003091	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0005368	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0006480	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0012170	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0025615	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0100491	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0100537	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0100725	ORPHA:642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000736	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000752	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000978	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001279	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001510	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001903	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0001955	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002015	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002100	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002270	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002936	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0003028	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0003095	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0003272	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0003474	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0004302	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0004926	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0008000	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0009085	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0010885	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0011968	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0030757	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0030811	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0100710	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0100712	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0100851	ORPHA:642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000559	ORPHA:642	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0000975	ORPHA:642	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0002045	ORPHA:642	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0012622	ORPHA:642	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0012804	ORPHA:642	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:642	Hereditary sensory and autonomic neuropathy type 4		HP:0100963	ORPHA:642	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000648	ORPHA:324737	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001249	ORPHA:324737	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001263	ORPHA:324737	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0003642	ORPHA:324737	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000518	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000572	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000589	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000639	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001251	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001317	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001935	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001999	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0007766	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0008064	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0008947	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0012443	ORPHA:324737	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000510	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000821	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000824	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0000982	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001250	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001272	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001928	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0001976	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0002334	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0002808	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0002910	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0005107	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0005585	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG		HP:0030680	ORPHA:324737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG	NOT	HP:0000365	ORPHA:324737	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG	NOT	HP:0000677	ORPHA:324737	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:324737	SRD5A3-CDG	NOT	HP:0001595	ORPHA:324737	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0009063	ORPHA:641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0001315	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0002380	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0002922	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0003323	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0003394	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0003690	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0004302	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0004345	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0006251	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0009077	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:641	Multifocal motor neuropathy		HP:0012078	ORPHA:641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000028	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000154	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000175	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000204	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000219	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000252	ORPHA:261236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000319	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000369	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000384	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000407	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000413	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000463	ORPHA:261236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000494	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000722	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000750	ORPHA:261236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0000767	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001263	ORPHA:261236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001274	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001276	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001328	ORPHA:261236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001360	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001629	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001631	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0001762	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0002020	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0002119	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0002197	ORPHA:261236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0002263	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0002269	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0002353	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0003196	ORPHA:261236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0004322	ORPHA:261236	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0005280	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0009914	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0010508	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0010864	ORPHA:261236	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0011968	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0100490	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0100716	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261236	16p13.11 microdeletion syndrome		HP:0100753	ORPHA:261236	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0000819	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0001272	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0002059	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0002066	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0002522	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0004322	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0004325	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0006827	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0007108	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0007141	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0007366	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0008619	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0010871	ORPHA:445062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0001256	ORPHA:445062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:445062	Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome		HP:0003487	ORPHA:445062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0000648	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0001138	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0001256	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0001257	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0001347	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0001762	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0002061	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0002079	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0002313	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0002936	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0003202	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0003383	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0003448	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0003484	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0003487	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0007010	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0007042	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0007340	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0007663	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0008963	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0009027	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0009830	ORPHA:320375	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0000486	ORPHA:320375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0000602	ORPHA:320375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0001999	ORPHA:320375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0002804	ORPHA:320375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320375	Autosomal recessive spastic paraplegia type 55		HP:0100543	ORPHA:320375	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0000164	ORPHA:1094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0000252	ORPHA:1094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0000340	ORPHA:1094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0000670	ORPHA:1094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0001798	ORPHA:1094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0004209	ORPHA:1094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0007598	ORPHA:1094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1094	Anonychia-microcephaly syndrome		HP:0010624	ORPHA:1094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309108	Pancreatic colipase deficiency		HP:0001081	ORPHA:309108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309108	Pancreatic colipase deficiency	NOT	HP:0001510	ORPHA:309108	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:309108	Pancreatic colipase deficiency		HP:0001738	ORPHA:309108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309108	Pancreatic colipase deficiency		HP:0001889	ORPHA:309108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309108	Pancreatic colipase deficiency		HP:0002028	ORPHA:309108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309108	Pancreatic colipase deficiency		HP:0002570	ORPHA:309108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309108	Pancreatic colipase deficiency		HP:0002630	ORPHA:309108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000027	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000054	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000077	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000105	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000135	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000204	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000212	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000141	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000238	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000293	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000365	ORPHA:168569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000520	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000534	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000771	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000819	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000823	ORPHA:168569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000953	ORPHA:168569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0008064	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0000998	ORPHA:168569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001084	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001256	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001433	ORPHA:168569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001596	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001763	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001822	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001935	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001954	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002024	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002110	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002155	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002257	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002619	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002716	ORPHA:168569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002750	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002757	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0002797	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0004322	ORPHA:168569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0003765	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0001347	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0007380	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0008734	ORPHA:168569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0009125	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0011025	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0012385	ORPHA:168569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0012724	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0030053	ORPHA:168569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0100324	ORPHA:168569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0100727	ORPHA:168569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0100776	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168569	H syndrome		HP:0100790	ORPHA:168569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0002064	ORPHA:320370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0002313	ORPHA:320370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0001288	ORPHA:320370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0002460	ORPHA:320370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0003487	ORPHA:320370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0003693	ORPHA:320370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0007010	ORPHA:320370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0001257	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0001290	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0001348	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0001761	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0002495	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0003438	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0006380	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0006466	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0007083	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320370	Autosomal recessive spastic paraplegia type 43		HP:0012785	ORPHA:320370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0030430	ORPHA:637	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000407	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000478	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002196	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002858	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0007663	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0007787	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0009589	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0009593	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0010302	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0100009	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0100963	ORPHA:637	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000238	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000360	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000572	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000587	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000618	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000646	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000651	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000763	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0000953	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0001250	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0001260	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0001269	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0001271	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0001317	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002015	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002172	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002317	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002354	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002512	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002888	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0003474	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0006824	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0008069	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0009027	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0009594	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0009831	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0010628	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0031189	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0100010	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0100014	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0100019	ORPHA:637	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0002381	ORPHA:637	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0007968	ORPHA:637	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0009592	ORPHA:637	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:637	Full NF2-related schwannomatosis		HP:0009733	ORPHA:637	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000707	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000823	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000995	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001012	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001256	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001328	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001482	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002858	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0007440	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0007565	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0008069	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0009592	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0009732	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0009737	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0012733	ORPHA:636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000028	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000098	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000364	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000365	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000478	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000504	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000520	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000997	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001100	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001251	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002167	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002315	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002354	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002652	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002757	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002857	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0003100	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0003401	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0007018	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0030052	ORPHA:636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000238	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000256	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000492	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000501	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000505	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000512	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000518	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000545	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000567	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000729	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000818	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000822	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000826	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000924	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0000938	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001053	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001250	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001387	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002086	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002650	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002664	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002666	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002808	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002970	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0003272	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0004322	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0005506	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0007378	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0007703	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0007957	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0009734	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0009735	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0010786	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0010935	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0011362	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0100013	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0100242	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0100545	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0100723	ORPHA:636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0001909	ORPHA:636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0002859	ORPHA:636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:636	Neurofibromatosis type 1		HP:0100570	ORPHA:636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000028	ORPHA:638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000271	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000316	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000358	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000465	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000494	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000508	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0000765	ORPHA:638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0001328	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0001639	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0001642	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0002015	ORPHA:638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0003010	ORPHA:638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0004322	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0007565	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0009023	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0011039	ORPHA:638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:638	Neurofibromatosis-Noonan syndrome		HP:0100763	ORPHA:638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000347	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000348	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000457	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000592	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000684	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000691	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000818	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000823	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000929	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0000966	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001156	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001249	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001270	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001620	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001831	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001943	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001956	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0001999	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0002750	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0002758	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0003124	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0003510	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0005281	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0007495	ORPHA:633	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0008736	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0009804	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0009811	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0009891	ORPHA:633	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:633	Laron syndrome		HP:0009924	ORPHA:633	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002921	ORPHA:449427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0010652	ORPHA:449427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002315	ORPHA:449427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002922	ORPHA:449427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0007340	ORPHA:449427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0011227	ORPHA:449427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0012531	ORPHA:449427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0032300	ORPHA:449427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0000123	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0000246	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0000572	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0000587	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0000651	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0000738	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0001250	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0001268	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0001289	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0001733	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002015	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002088	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002094	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002176	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002381	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002385	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0002840	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0003319	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0003419	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0003474	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0006824	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0009744	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0009911	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0010558	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0011850	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0030833	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0045052	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:3000035	ORPHA:449427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0000929	ORPHA:449427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0001880	ORPHA:449427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449427	IgG4-related pachymeningitis		HP:0004431	ORPHA:449427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0003006	ORPHA:635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0004375	ORPHA:635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0011976	ORPHA:635	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001824	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001873	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001903	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001945	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0002028	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0002716	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0003270	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0003334	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0012378	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0031500	ORPHA:635	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0000520	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0000737	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001017	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001482	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001892	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001928	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0002098	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0002176	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0002277	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0002653	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0002756	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0003281	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0011977	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0011978	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0025435	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0031955	ORPHA:635	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0000822	ORPHA:635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001251	ORPHA:635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0001336	ORPHA:635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0010543	ORPHA:635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:635	Neuroblastoma		HP:0025553	ORPHA:635	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000013	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000026	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000055	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000133	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000142	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000786	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000789	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000837	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0001271	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0001315	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0002460	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0003130	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0003134	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0003202	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0003409	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0003434	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0007141	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0008214	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0008715	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0008723	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0010464	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0040171	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0045010	ORPHA:168563	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0000150	ORPHA:168563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0001761	ORPHA:168563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:168563	46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome		HP:0003376	ORPHA:168563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0000956	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0000964	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0001025	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0001595	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0002024	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0002099	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0002209	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0002213	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0003212	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0007400	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0007479	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0008064	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0009886	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0100326	ORPHA:634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0001249	ORPHA:634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0001250	ORPHA:634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0001263	ORPHA:634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0002097	ORPHA:634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0002205	ORPHA:634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0004313	ORPHA:634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0000086	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0000126	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0000653	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0000958	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0000988	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0001019	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0001944	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0002719	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0003355	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0004322	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:634	Netherton syndrome		HP:0045075	ORPHA:634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000750	ORPHA:261229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0012758	ORPHA:261229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000252	ORPHA:261229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000718	ORPHA:261229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0001249	ORPHA:261229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0001290	ORPHA:261229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0001513	ORPHA:261229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0002591	ORPHA:261229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0007018	ORPHA:261229	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000286	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000316	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000347	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000431	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000666	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000717	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000821	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0000956	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0001250	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0001350	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0002263	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0002360	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0002553	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0005280	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261229	14q11.2 microduplication syndrome		HP:0008872	ORPHA:261229	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0000083	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0000124	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0000648	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001249	ORPHA:289916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001254	ORPHA:289916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001259	ORPHA:289916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001263	ORPHA:289916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001252	ORPHA:289916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001266	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001332	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001510	ORPHA:289916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001733	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001873	ORPHA:289916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001875	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001903	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0001987	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0002017	ORPHA:289916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0002072	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0002098	ORPHA:289916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0002240	ORPHA:289916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0004374	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289916	Vitamin B12-unresponsive methylmalonic acidemia type mut0		HP:0100806	ORPHA:289916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000076	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000077	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000093	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000104	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000160	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000294	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000300	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000426	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000510	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000556	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000729	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0000750	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0001263	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0001166	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0001249	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0001250	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0001319	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0001513	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0002076	ORPHA:261222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0002149	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0002251	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0002808	ORPHA:261222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0007018	ORPHA:261222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0011351	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0012450	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261222	Distal 16p11.2 microdeletion syndrome		HP:0012622	ORPHA:261222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0005328	ORPHA:435628	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0009059	ORPHA:435628	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000194	ORPHA:435628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000252	ORPHA:435628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000322	ORPHA:435628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000347	ORPHA:435628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001249	ORPHA:435628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001347	ORPHA:435628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0100678	ORPHA:435628	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000212	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000218	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000290	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000292	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000298	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000430	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000446	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000496	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000520	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0000586	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001090	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001276	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001285	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001371	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001508	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001561	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0002093	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0002094	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0002179	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0002187	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0002650	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0002781	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0005274	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0006532	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0008734	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0008897	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0009125	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0009933	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0010751	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0010804	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0011344	ORPHA:435628	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0001250	ORPHA:435628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435628	Keppen-Lubinsky syndrome		HP:0002659	ORPHA:435628	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0000648	ORPHA:320406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0002828	ORPHA:320406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0003693	ORPHA:320406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0000543	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0000975	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0001260	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0001761	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0002166	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0002194	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0002267	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0001288	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0002600	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0002650	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0003380	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0003477	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0007020	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0007054	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0008944	ORPHA:320406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0000639	ORPHA:320406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320406	Spastic paraplegia-optic atrophy-neuropathy syndrome		HP:0002071	ORPHA:320406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0000077	ORPHA:284227	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0001009	ORPHA:284227	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0001899	ORPHA:284227	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0003237	ORPHA:284227	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0012418	ORPHA:284227	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0001028	ORPHA:284227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0001541	ORPHA:284227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0004930	ORPHA:284227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0011920	ORPHA:284227	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0001901	ORPHA:284227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0002170	ORPHA:284227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0004936	ORPHA:284227	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0001041	ORPHA:284227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284227	TEMPI syndrome		HP:0002315	ORPHA:284227	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0000505	ORPHA:254930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0000648	ORPHA:254930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0003202	ORPHA:254930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0000602	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001123	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001263	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001508	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001761	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002313	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001288	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002395	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002936	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0003477	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0003693	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0007256	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0007340	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0031629	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0100543	ORPHA:254930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0000508	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0000639	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001251	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001260	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001283	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001284	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0001349	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002079	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002376	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002500	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002540	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002590	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0002943	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0003380	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0003484	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0005216	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0007641	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0008947	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0011471	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0012696	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0012707	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0012747	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0020049	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254930	Combined oxidative phosphorylation defect type 7		HP:0200136	ORPHA:254930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0000486	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0000649	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0001251	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0001260	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0001761	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0002061	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0003429	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0006958	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0007377	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0012896	ORPHA:320401	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0000407	ORPHA:320401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0001250	ORPHA:320401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0001288	ORPHA:320401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0002839	ORPHA:320401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0003474	ORPHA:320401	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320401	Autosomal recessive spastic paraplegia type 44		HP:0002194	ORPHA:320401	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001945	ORPHA:707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002840	ORPHA:707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0012378	ORPHA:707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0000739	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0000958	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001649	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001744	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002039	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002240	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002315	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0004372	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0008066	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0011355	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0020084	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0025143	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0030953	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0031258	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0031864	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0100749	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0200042	ORPHA:707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0000206	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0000365	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0000716	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0000969	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0000988	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001259	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001350	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001892	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002013	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002014	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002027	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002037	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002098	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002105	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002248	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002317	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002615	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0002829	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0004387	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0009811	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0011499	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0011675	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0011949	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0012219	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0025043	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0025085	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0032564	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0040181	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0100806	ORPHA:707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001287	ORPHA:707	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001324	ORPHA:707	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0001369	ORPHA:707	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0025439	ORPHA:707	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0100533	ORPHA:707	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:707	Plague		HP:0100584	ORPHA:707	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000219	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000248	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000276	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000311	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000343	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000347	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000470	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000501	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000659	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001156	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001249	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001263	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001511	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001773	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001831	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0002000	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0002263	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0002983	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0004209	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0007833	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0007957	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0008873	ORPHA:709	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000028	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000047	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000175	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000204	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000238	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000316	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000384	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000465	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000482	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000504	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000518	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000582	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000639	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000687	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001558	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001642	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001671	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001770	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0002007	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0004322	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0004414	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0004467	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0008569	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0008872	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0008897	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0011220	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0012745	ORPHA:709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000003	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000013	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000023	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000060	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000073	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000075	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000126	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000154	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000252	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000358	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000405	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000463	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000505	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000648	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000830	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000851	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000960	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001537	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001561	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0001643	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0002023	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0002119	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0002120	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0003196	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0003298	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0005280	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0006610	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0007370	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0000612	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0008678	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0008905	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0100819	ORPHA:709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0004383	ORPHA:709	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0005182	ORPHA:709	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:709	Peters plus syndrome		HP:0030968	ORPHA:709	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0000659	ORPHA:708	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0000523	ORPHA:708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0007759	ORPHA:708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0011483	ORPHA:708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0011493	ORPHA:708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0031159	ORPHA:708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0001087	ORPHA:708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0000486	ORPHA:708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:708	Peters anomaly		HP:0000639	ORPHA:708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0000819	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0000964	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0001025	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0001824	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0002719	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0002960	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0008066	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0010783	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0012733	ORPHA:703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0000989	ORPHA:703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0003765	ORPHA:703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0033106	ORPHA:703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:4000019	ORPHA:703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:4000020	ORPHA:703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:703	Bullous pemphigoid		HP:0200097	ORPHA:703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0001822	ORPHA:93397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0001852	ORPHA:93397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0004691	ORPHA:93397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009843	ORPHA:93397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0010109	ORPHA:93397	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0004209	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0008096	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009464	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009467	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009523	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009536	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009576	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009642	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0009700	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0010348	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0011304	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93397	Brachydactyly type A7		HP:0100394	ORPHA:93397	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0002376	ORPHA:293181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0002540	ORPHA:293181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0004302	ORPHA:293181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0010841	ORPHA:293181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0012758	ORPHA:293181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0100543	ORPHA:293181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0000252	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0001252	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0002059	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0002069	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0002384	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0006813	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0007334	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0010821	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0032794	ORPHA:293181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0000505	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0001273	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0001276	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0001508	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0002521	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0002650	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0011097	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0012448	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0031834	ORPHA:293181	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293181	Epilepsy of infancy with migrating focal seizures		HP:0000826	ORPHA:293181	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000079	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000252	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000365	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000505	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000639	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000648	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000649	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0000708	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001249	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001250	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001251	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001252	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001257	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001266	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001288	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001332	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001387	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001531	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0001622	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002093	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002120	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002167	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002205	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002376	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002607	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002650	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0002808	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0004322	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0004326	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0009830	ORPHA:702	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0100022	ORPHA:702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:702	Pelizaeus-Merzbacher disease		HP:0100026	ORPHA:702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0000359	ORPHA:705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0000407	ORPHA:705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0008586	ORPHA:705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0011387	ORPHA:705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0000821	ORPHA:705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0000853	ORPHA:705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0000112	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0000843	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0001249	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0001251	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0002093	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0002167	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0002321	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0002777	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:705	Pendred syndrome		HP:0002890	ORPHA:705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0000987	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0001025	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0001824	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0002719	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0002960	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0008872	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0031446	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0100792	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0100838	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0200097	ORPHA:704	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0000716	ORPHA:704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0000739	ORPHA:704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0008066	ORPHA:704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0011968	ORPHA:704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0034194	ORPHA:704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:4000013	ORPHA:704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:4000014	ORPHA:704	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0002293	ORPHA:704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0012531	ORPHA:704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:704	Pemphigus vulgaris		HP:0030351	ORPHA:704	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93396	Brachydactyly type A2		HP:0001773	ORPHA:93396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93396	Brachydactyly type A2		HP:0004209	ORPHA:93396	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93396	Brachydactyly type A2		HP:0004220	ORPHA:93396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93396	Brachydactyly type A2		HP:0005819	ORPHA:93396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93396	Brachydactyly type A2		HP:0009372	ORPHA:93396	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93396	Brachydactyly type A2		HP:0009568	ORPHA:93396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93396	Brachydactyly type A2		HP:0010038	ORPHA:93396	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0000561	ORPHA:701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0002223	ORPHA:701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0002232	ORPHA:701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0002289	ORPHA:701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0000820	ORPHA:701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0000822	ORPHA:701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0001047	ORPHA:701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0001597	ORPHA:701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0002960	ORPHA:701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0003119	ORPHA:701	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0001045	ORPHA:701	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0003765	ORPHA:701	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:701	Alopecia universalis		HP:0100651	ORPHA:701	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000280	ORPHA:93399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000943	ORPHA:93399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001263	ORPHA:93399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0003271	ORPHA:93399	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000365	ORPHA:93399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000518	ORPHA:93399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001250	ORPHA:93399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0008947	ORPHA:93399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0010729	ORPHA:93399	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000023	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000077	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000212	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000369	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000486	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000572	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000639	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0000648	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001251	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001257	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001270	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001310	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001336	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001433	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001537	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001618	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0001627	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0002015	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0002061	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0002086	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0002123	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0002240	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0002505	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0003312	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0004554	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0007957	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0009891	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0010808	ORPHA:93399	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93399	Juvenile sialidosis type 2		HP:0010864	ORPHA:93399	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0002293	ORPHA:700	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0007418	ORPHA:700	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0001045	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0001803	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0001806	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0001808	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0002037	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0002960	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0030804	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:700	Alopecia totalis		HP:0100651	ORPHA:700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93394	Brachydactyly type A4		HP:0001762	ORPHA:93394	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93394	Brachydactyly type A4		HP:0004220	ORPHA:93394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93394	Brachydactyly type A4		HP:0004322	ORPHA:93394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93394	Brachydactyly type A4		HP:0006239	ORPHA:93394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93394	Brachydactyly type A4		HP:0009577	ORPHA:93394	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93394	Brachydactyly type A4		HP:0009773	ORPHA:93394	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000194	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000202	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000276	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000286	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000308	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000348	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000365	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000369	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000377	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000389	ORPHA:261211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000414	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000463	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000486	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000490	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000494	ORPHA:261211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000581	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000601	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000750	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0000752	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0001252	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0001263	ORPHA:261211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0001511	ORPHA:261211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0001770	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0002007	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0002020	ORPHA:261211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0002342	ORPHA:261211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0002360	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0003189	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0003196	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0004279	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0004322	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0005180	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0005285	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0007328	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0007565	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0007598	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0009623	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0010535	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0011675	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0011968	ORPHA:261211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0012368	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0100033	ORPHA:261211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261211	16p11.2p12.2 microdeletion syndrome		HP:0100490	ORPHA:261211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1195	Congenital atransferrinemia		HP:0000821	ORPHA:1195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1195	Congenital atransferrinemia		HP:0001369	ORPHA:1195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1195	Congenital atransferrinemia		HP:0001626	ORPHA:1195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1195	Congenital atransferrinemia		HP:0001732	ORPHA:1195	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1195	Congenital atransferrinemia		HP:0001903	ORPHA:1195	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1195	Congenital atransferrinemia		HP:0002719	ORPHA:1195	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140905	Hyperlipidemia due to hepatic triacylglycerol lipase deficiency		HP:0002155	ORPHA:140905	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:140905	Hyperlipidemia due to hepatic triacylglycerol lipase deficiency		HP:0012184	ORPHA:140905	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:140905	Hyperlipidemia due to hepatic triacylglycerol lipase deficiency		HP:0001013	ORPHA:140905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140905	Hyperlipidemia due to hepatic triacylglycerol lipase deficiency		HP:0001681	ORPHA:140905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140905	Hyperlipidemia due to hepatic triacylglycerol lipase deficiency		HP:0005181	ORPHA:140905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000028	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000047	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000077	ORPHA:1194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000154	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000252	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000278	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000322	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0000369	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001250	ORPHA:1194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001252	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001371	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001510	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001511	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001522	ORPHA:1194	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001562	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001635	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001639	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001641	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001646	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0001987	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0002120	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0002240	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0002342	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0002383	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0002878	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0003535	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0007370	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0011343	ORPHA:1194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0011675	ORPHA:1194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1194	TMEM70-related mitochondrial encephalo-cardio-myopathy		HP:0100490	ORPHA:1194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000053	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000164	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000232	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000256	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000280	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000316	ORPHA:1193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000336	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000337	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000400	ORPHA:1193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000455	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0000463	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0001249	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0001513	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0001593	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0004322	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1193	Atkin-Flaitz syndrome		HP:0012471	ORPHA:1193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0000407	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001327	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001677	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001903	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0002344	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0003287	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0004322	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0007201	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0100651	ORPHA:1192	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0000028	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0000093	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0000100	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0000112	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0000822	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001276	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001288	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001337	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001376	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0001633	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0002120	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0003307	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0007360	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1192	Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome		HP:0100545	ORPHA:1192	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0001773	ORPHA:140908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0001817	ORPHA:140908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0001831	ORPHA:140908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0001857	ORPHA:140908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0005048	ORPHA:140908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0005831	ORPHA:140908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0006101	ORPHA:140908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0009773	ORPHA:140908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140908	Brachydactyly type B2		HP:0009882	ORPHA:140908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000774	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0001156	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0001762	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0002089	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0002991	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0003097	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0003417	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0004599	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0005257	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0008905	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0009107	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0009826	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0011800	ORPHA:1190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000175	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000316	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000347	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000369	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000506	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000520	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0000926	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0001373	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0001561	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0001602	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0002280	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0002650	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0003026	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0004785	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0004894	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0005562	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0007973	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0008857	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1190	Atelosteogenesis type I		HP:0030992	ORPHA:1190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0000713	ORPHA:276608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0000825	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0000842	ORPHA:276608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0000975	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0000980	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0001249	ORPHA:276608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0001250	ORPHA:276608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0001254	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0001259	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0002315	ORPHA:276608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0001337	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0001649	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0001985	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0002329	ORPHA:276608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0002344	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0003162	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0003324	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0004324	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0004510	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0012051	ORPHA:276608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276608	Non-insulinoma pancreatogenous hypoglycemia syndrome		HP:0012378	ORPHA:276608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0000707	ORPHA:79093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0002196	ORPHA:79093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0004947	ORPHA:79093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0012703	ORPHA:79093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0012721	ORPHA:79093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0040272	ORPHA:79093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0100561	ORPHA:79093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0001284	ORPHA:79093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0001324	ORPHA:79093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0001347	ORPHA:79093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0003418	ORPHA:79093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0007199	ORPHA:79093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0012486	ORPHA:79093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0000009	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0000011	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0000016	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0000020	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0002141	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0002317	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0001288	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0002359	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0002607	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0003401	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0003419	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0003474	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0007340	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0009053	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0012423	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0012534	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0030014	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0040307	ORPHA:79093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0002318	ORPHA:79093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79093	Foix-Alajouanine syndrome		HP:0008944	ORPHA:79093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0000822	ORPHA:79094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0001159	ORPHA:79094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0001328	ORPHA:79094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0001629	ORPHA:79094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0001643	ORPHA:79094	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0001659	ORPHA:79094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0002659	ORPHA:79094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0004279	ORPHA:79094	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0006889	ORPHA:79094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79094	Grange syndrome		HP:0100545	ORPHA:79094	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002575	ORPHA:1199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001531	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002013	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002015	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002091	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002205	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002579	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0003781	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0006510	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0008872	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0010963	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0012387	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0012523	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0100326	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0100633	ORPHA:1199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000079	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000119	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000961	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000980	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001510	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001518	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001561	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001604	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001607	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002020	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002021	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002098	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002835	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0003468	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0004885	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0008755	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0012252	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0012718	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0012732	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0030084	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0030680	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0040064	ORPHA:1199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000104	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000175	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000365	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000453	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000589	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000598	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0000811	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001252	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001276	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001539	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001629	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001636	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001680	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0001999	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002089	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002247	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002566	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002650	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0002672	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0008751	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0009800	ORPHA:1199	TAS		HP:0040284			H	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0100580	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1199	Esophageal atresia		HP:0410030	ORPHA:1199	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0001539	ORPHA:1198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0001543	ORPHA:1198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0003270	ORPHA:1198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0003363	ORPHA:1198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0004398	ORPHA:1198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0010448	ORPHA:1198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0100016	ORPHA:1198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1198	Colonic atresia		HP:0100867	ORPHA:1198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0003236	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0005978	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0011892	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0030516	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0100753	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0200084	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0012379	ORPHA:79095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0000580	ORPHA:79095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0001250	ORPHA:79095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0001298	ORPHA:79095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0001328	ORPHA:79095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0007141	ORPHA:79095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0000135	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0000518	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0000716	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0000763	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0001081	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0001251	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0001268	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0001337	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0002076	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0002354	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0002401	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0002573	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0002611	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0002910	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79095	Congenital bile acid synthesis defect type 4		HP:0003201	ORPHA:79095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0002133	ORPHA:79096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0200134	ORPHA:79096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0000496	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001250	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001263	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001276	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001336	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001508	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001560	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001622	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001942	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0001943	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0002151	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0002283	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0002317	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0003785	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0005961	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0008936	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0010851	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0011968	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0025430	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0030917	ORPHA:79096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0000252	ORPHA:79096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0005522	ORPHA:79096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0010895	ORPHA:79096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0010900	ORPHA:79096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0010904	ORPHA:79096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0010909	ORPHA:79096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79096	Pyridoxamine-5-phosphate deficiency-developmental and epileptic encephalopathy		HP:0010917	ORPHA:79096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001250	ORPHA:79097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001251	ORPHA:79097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001263	ORPHA:79097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0012446	ORPHA:79097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0000708	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0000729	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001272	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001298	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002098	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0003270	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0004302	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0006808	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0010841	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0010845	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0012448	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0040204	ORPHA:79097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0000407	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0000545	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0000648	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0000737	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001276	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001285	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001332	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001347	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002072	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002104	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002123	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002133	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002136	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0001288	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002360	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002376	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002465	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0002521	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0006892	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0010819	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0020221	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79097	Folinic acid-responsive seizures		HP:0100022	ORPHA:79097	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0007663	ORPHA:79098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0000501	ORPHA:79098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0000518	ORPHA:79098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0000541	ORPHA:79098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0011531	ORPHA:79098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0025341	ORPHA:79098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0025560	ORPHA:79098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0030823	ORPHA:79098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0000360	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0000365	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0000573	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0000613	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0001045	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0001085	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0001596	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0002290	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0002315	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0007680	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0007906	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0010783	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0011484	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0012123	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0040049	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0100832	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:0200026	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79098	Sympathetic ophthalmia		HP:6000710	ORPHA:79098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0000256	ORPHA:93387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0002007	ORPHA:93387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0004322	ORPHA:93387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0001382	ORPHA:93387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0005863	ORPHA:93387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0009882	ORPHA:93387	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0010049	ORPHA:93387	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0010076	ORPHA:93387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0010743	ORPHA:93387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93387	Brachydactyly type E		HP:0100560	ORPHA:93387	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0001370	ORPHA:79099	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0010783	ORPHA:79099	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0003565	ORPHA:79099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0011123	ORPHA:79099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0011227	ORPHA:79099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0200034	ORPHA:79099	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0002923	ORPHA:79099	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79099	Interstitial granulomatous dermatitis with arthritis		HP:0000989	ORPHA:79099	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0001231	ORPHA:93384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0004209	ORPHA:93384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0004322	ORPHA:93384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0005819	ORPHA:93384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0009373	ORPHA:93384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0009465	ORPHA:93384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0009495	ORPHA:93384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0009606	ORPHA:93384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0009684	ORPHA:93384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0009773	ORPHA:93384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0010026	ORPHA:93384	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0010508	ORPHA:93384	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0010579	ORPHA:93384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93384	Brachydactyly type C		HP:0010743	ORPHA:93384	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0001974	ORPHA:293173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0200039	ORPHA:293173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0000989	ORPHA:293173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0001880	ORPHA:293173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0001945	ORPHA:293173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0003565	ORPHA:293173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0011897	ORPHA:293173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0032022	ORPHA:293173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0040189	ORPHA:293173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0000083	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0000282	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0000979	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0001396	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0002094	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0002910	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0031236	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0100792	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0100825	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0200037	ORPHA:293173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0000509	ORPHA:293173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0000953	ORPHA:293173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0001875	ORPHA:293173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:293173	Acute generalized exanthematous pustulosis		HP:0002716	ORPHA:293173	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0001204	ORPHA:93388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0001230	ORPHA:93388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0001762	ORPHA:93388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0001773	ORPHA:93388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0002650	ORPHA:93388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0003022	ORPHA:93388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0004209	ORPHA:93388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0004322	ORPHA:93388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0005819	ORPHA:93388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0009778	ORPHA:93388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0010109	ORPHA:93388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93388	Brachydactyly type A1		HP:0010579	ORPHA:93388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0000218	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0001270	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0001284	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0001290	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0001763	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003198	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003325	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003403	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003473	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003701	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0030191	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0030202	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0030205	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0100301	ORPHA:353327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0000508	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0001371	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0001382	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0001288	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0002359	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0002421	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0002515	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0002650	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0002938	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003200	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003236	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003388	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003391	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003394	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003551	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003691	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0003803	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0006380	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0009028	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0009046	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0010628	ORPHA:353327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:353327	Congenital myasthenic syndromes with glycosylation defect		HP:0002460	ORPHA:353327	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0000047	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0000175	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0000252	ORPHA:261204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0000545	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0000709	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0000717	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0000767	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0001249	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0001250	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0001263	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0001332	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0002463	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0007018	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261204	16p11.2p12.2 microduplication syndrome		HP:0100753	ORPHA:261204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0000083	ORPHA:730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0000107	ORPHA:730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0001407	ORPHA:730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0003259	ORPHA:730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0012213	ORPHA:730	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0000790	ORPHA:730	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0000822	ORPHA:730	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0003774	ORPHA:730	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0012591	ORPHA:730	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0012592	ORPHA:730	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0012622	ORPHA:730	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0030157	ORPHA:730	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0000010	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0000105	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0000791	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0001634	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0001737	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0002616	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0004944	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0006557	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0008672	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0011004	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0012207	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0012330	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0100702	ORPHA:730	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:730	Autosomal dominant polycystic kidney disease		HP:0011760	ORPHA:730	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0001508	ORPHA:92050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0002024	ORPHA:92050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0002028	ORPHA:92050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0011473	ORPHA:92050	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0000737	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0001824	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0001944	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0002570	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0003270	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0005208	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0025129	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0032486	ORPHA:92050	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0000518	ORPHA:92050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0000613	ORPHA:92050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0000951	ORPHA:92050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0001369	ORPHA:92050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0025090	ORPHA:92050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0200020	ORPHA:92050	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0000202	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0000453	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0000588	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0002013	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0002023	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0002611	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0002652	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:92050	Congenital tufting enteropathy		HP:0011859	ORPHA:92050	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0001773	ORPHA:93383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0001817	ORPHA:93383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0005831	ORPHA:93383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0008083	ORPHA:93383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0009882	ORPHA:93383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0010049	ORPHA:93383	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0005048	ORPHA:93383	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0006101	ORPHA:93383	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0009773	ORPHA:93383	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93383	Brachydactyly type B		HP:0010059	ORPHA:93383	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0000218	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0000958	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0000992	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0001025	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0001251	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0001315	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0004209	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0004322	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0007598	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0100022	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0100543	ORPHA:1184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0000164	ORPHA:1184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0000486	ORPHA:1184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0001288	ORPHA:1184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0002967	ORPHA:1184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1184	Ataxia-photosensitivity-short stature syndrome		HP:0030680	ORPHA:1184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0000570	ORPHA:1183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0001251	ORPHA:1183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0001336	ORPHA:1183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0002360	ORPHA:1183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0010543	ORPHA:1183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0000708	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0000737	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0002321	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0002664	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0003006	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0045084	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0100543	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:5000002	ORPHA:1183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0001298	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0002063	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0002861	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0003002	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0012226	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0030057	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0030357	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0031035	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1183	Opsoclonus-myoclonus syndrome		HP:0100526	ORPHA:1183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0000639	ORPHA:1182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0001250	ORPHA:1182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0001251	ORPHA:1182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0001260	ORPHA:1182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0001347	ORPHA:1182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0002497	ORPHA:1182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0004374	ORPHA:1182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1182	Spastic ataxia with congenital miosis		HP:0007728	ORPHA:1182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1180	Ataxia-hypogonadism-choroidal dystrophy syndrome		HP:0000044	ORPHA:1180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1180	Ataxia-hypogonadism-choroidal dystrophy syndrome		HP:0001135	ORPHA:1180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1180	Ataxia-hypogonadism-choroidal dystrophy syndrome		HP:0001251	ORPHA:1180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001250	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001251	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001252	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001270	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001298	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001324	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001639	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001644	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001987	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0002098	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0003128	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0003348	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0003535	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0009830	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0011675	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0012758	ORPHA:254913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000089	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000135	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000252	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000407	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000486	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000508	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000510	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000518	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000618	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000639	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000648	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000821	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001254	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001258	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001260	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001272	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0001332	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0002120	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0002240	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0002445	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0003546	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0004322	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0032794	ORPHA:254913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254913	Isolated ATP synthase deficiency		HP:0000602	ORPHA:254913	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000956	ORPHA:140936	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000966	ORPHA:140936	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0008070	ORPHA:140936	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000153	ORPHA:140936	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000221	ORPHA:140936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000668	ORPHA:140936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000972	ORPHA:140936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0001249	ORPHA:140936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0008404	ORPHA:140936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0010802	ORPHA:140936	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000276	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000303	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000577	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000582	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0000670	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0001045	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0001620	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0005338	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0007646	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0008388	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0011367	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140936	Lelis syndrome		HP:0011800	ORPHA:140936	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140941	Short stature due to primary acid-labile subunit deficiency		HP:0000347	ORPHA:140941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140941	Short stature due to primary acid-labile subunit deficiency		HP:0000823	ORPHA:140941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140941	Short stature due to primary acid-labile subunit deficiency		HP:0002750	ORPHA:140941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140941	Short stature due to primary acid-labile subunit deficiency		HP:0000855	ORPHA:140941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140941	Short stature due to primary acid-labile subunit deficiency		HP:0001510	ORPHA:140941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140941	Short stature due to primary acid-labile subunit deficiency		HP:0001956	ORPHA:140941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140941	Short stature due to primary acid-labile subunit deficiency		HP:0030353	ORPHA:140941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0009126	ORPHA:140944	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0025104	ORPHA:140944	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0000324	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001169	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001528	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001782	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001852	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0002650	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0004099	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0009487	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0010816	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0012721	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0100555	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0100766	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0430028	ORPHA:140944	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0000107	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0000689	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0000767	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0000965	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001249	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001250	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001288	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001977	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0002126	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0002414	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0002435	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0002475	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0002999	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0007206	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0007340	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0007370	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0008678	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0010442	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0010609	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0012531	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0012725	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0025476	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0031287	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0033794	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0100026	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0100559	ORPHA:140944	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0001385	ORPHA:140944	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:140944	CLOVES syndrome		HP:0002667	ORPHA:140944	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0000174	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0000407	ORPHA:1188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0000486	ORPHA:1188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0000639	ORPHA:1188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0000762	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0001249	ORPHA:1188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0001251	ORPHA:1188	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0001252	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0001315	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0002119	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0002120	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0002167	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0002650	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0003202	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0003457	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0001382	ORPHA:1188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1188	Ataxia-deafness-intellectual disability syndrome		HP:0007360	ORPHA:1188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0000225	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0000360	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0000421	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0000822	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0000978	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001681	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001744	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001824	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001901	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002027	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002240	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002315	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002321	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002488	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002863	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0011974	ORPHA:729	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0000504	ORPHA:729	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002093	ORPHA:729	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002829	ORPHA:729	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0003401	ORPHA:729	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0012378	ORPHA:729	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0000989	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001297	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001409	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001894	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0001974	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002204	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002239	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0002639	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0004417	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0004420	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0004936	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0030242	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0032147	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:729	Polycythemia vera		HP:0033842	ORPHA:729	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000822	ORPHA:79083	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000855	ORPHA:79083	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0100578	ORPHA:79083	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000819	ORPHA:79083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000831	ORPHA:79083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000991	ORPHA:79083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0002155	ORPHA:79083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0002240	ORPHA:79083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0003635	ORPHA:79083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0008065	ORPHA:79083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000869	ORPHA:79083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000963	ORPHA:79083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0002621	ORPHA:79083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0003712	ORPHA:79083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000147	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000292	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000876	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000956	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0001397	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0001635	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0001639	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0001677	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0001733	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0001744	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0002149	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0002230	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0003198	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0003326	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0003707	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0009800	ORPHA:79083	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0012084	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0100601	ORPHA:79083	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0100607	ORPHA:79083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0000786	ORPHA:79083	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0001394	ORPHA:79083	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79083	PPARG-related familial partial lipodystrophy		HP:0007457	ORPHA:79083	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000518	ORPHA:728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001369	ORPHA:728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0005310	ORPHA:728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0100662	ORPHA:728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0200047	ORPHA:728	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000360	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001251	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001376	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001609	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001646	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001701	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002017	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002094	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002321	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002786	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0012735	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0030828	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0100750	ORPHA:728	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000083	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000093	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000407	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000491	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000509	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000520	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000554	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000790	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0000979	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001545	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001596	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001601	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0001686	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002617	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002793	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002829	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0002923	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0003493	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0004306	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0004418	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0004422	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0004936	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0006824	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0010783	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0011107	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0012115	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0012733	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0012819	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0031481	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0033380	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0100532	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0100533	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0100534	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0100758	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:728	Relapsing polychondritis		HP:0100820	ORPHA:728	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0000147	ORPHA:79084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0000819	ORPHA:79084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0000822	ORPHA:79084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0000842	ORPHA:79084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0000855	ORPHA:79084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0000956	ORPHA:79084	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0000991	ORPHA:79084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0001397	ORPHA:79084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0001677	ORPHA:79084	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0001733	ORPHA:79084	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0002240	ORPHA:79084	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79084	Familial partial lipodystrophy, Köbberling type		HP:0100578	ORPHA:79084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0000505	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0000618	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0000648	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0001324	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0002300	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0002719	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0002788	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0003431	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0003444	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0007258	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0007377	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0008527	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0030272	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0032169	ORPHA:1187	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0000467	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0000639	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0001251	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0001256	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0001270	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0001284	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0002342	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0002445	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0003537	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0004887	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0008311	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0008936	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0009830	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0011185	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0011476	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1187	Lethal ataxia with deafness and optic atrophy		HP:0012389	ORPHA:1187	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1186	Infantile-onset spinocerebellar ataxia		HP:0000365	ORPHA:1186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1186	Infantile-onset spinocerebellar ataxia		HP:0000602	ORPHA:1186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1186	Infantile-onset spinocerebellar ataxia		HP:0000648	ORPHA:1186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1186	Infantile-onset spinocerebellar ataxia		HP:0001251	ORPHA:1186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1186	Infantile-onset spinocerebellar ataxia		HP:0001315	ORPHA:1186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1186	Infantile-onset spinocerebellar ataxia		HP:0002270	ORPHA:1186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1186	Infantile-onset spinocerebellar ataxia		HP:0100022	ORPHA:1186	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0000855	ORPHA:79085	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0009125	ORPHA:79085	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0000956	ORPHA:79085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0001397	ORPHA:79085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0002155	ORPHA:79085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0002240	ORPHA:79085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0003292	ORPHA:79085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0008993	ORPHA:79085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0030685	ORPHA:79085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0000147	ORPHA:79085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0000831	ORPHA:79085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79085	AKT2-related familial partial lipodystrophy		HP:0000876	ORPHA:79085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000256	ORPHA:1185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000268	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000286	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000337	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000358	ORPHA:1185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000463	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000508	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000520	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000639	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000648	ORPHA:1185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0000974	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0001252	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0001263	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0002208	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0002714	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0002816	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0002967	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0003100	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0003196	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0003298	ORPHA:1185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0003457	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0004322	ORPHA:1185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0004349	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0001382	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0007360	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1185	Spinocerebellar ataxia-dysmorphism syndrome		HP:0012471	ORPHA:1185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0009064	ORPHA:79086	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0000842	ORPHA:79086	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0000855	ORPHA:79086	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0000831	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0001397	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0001638	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0002960	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0003119	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0003707	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0005328	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0011025	ORPHA:79086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0000093	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0000147	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0000822	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0000956	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0001394	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0001735	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0002155	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0002230	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0002240	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0003198	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0005339	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0005616	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0007440	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0012490	ORPHA:79086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0002665	ORPHA:79086	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0009592	ORPHA:79086	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79086	Acquired generalized lipodystrophy		HP:0012064	ORPHA:79086	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0100578	ORPHA:79087	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0000365	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0001249	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0001250	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0002960	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0003198	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0005328	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0005421	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0100827	ORPHA:79087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0000093	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0000855	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0001397	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0002230	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0002721	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0002829	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0002907	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79087	Acquired partial lipodystrophy		HP:0100820	ORPHA:79087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0001250	ORPHA:725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0011182	ORPHA:725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0031491	ORPHA:725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0001249	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002069	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002349	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002376	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002384	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0006813	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0007270	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0007359	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0011153	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0012010	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0012557	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0100543	ORPHA:725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0000718	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0000729	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0001332	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0001345	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002266	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002312	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002333	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002381	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0002487	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0009088	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0010819	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0011098	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0011147	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0011150	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:725	Developmental and epileptic encephalopathy with spike-wave activation in sleep		HP:0012001	ORPHA:725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0001945	ORPHA:724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0002091	ORPHA:724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0002093	ORPHA:724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0002113	ORPHA:724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0100749	ORPHA:724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0001879	ORPHA:724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0002027	ORPHA:724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0002103	ORPHA:724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0002793	ORPHA:724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0003326	ORPHA:724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:724	Idiopathic acute eosinophilic pneumonia		HP:0012735	ORPHA:724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0002668	ORPHA:276621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0006737	ORPHA:276621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0006748	ORPHA:276621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0000093	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0000096	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0000740	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001069	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001095	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001342	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001618	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001824	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001962	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0002018	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0002331	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0002574	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0002640	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0002864	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0003072	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0003345	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0003574	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0003639	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0008629	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0010532	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0011703	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0011979	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0012378	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0031284	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0100749	ORPHA:276621	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0000405	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0000790	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0000980	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001293	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001337	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001605	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0001635	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276621	Sporadic pheochromocytoma/secreting paraganglioma		HP:0025269	ORPHA:276621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000083	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000099	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000790	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000988	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001945	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002105	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002633	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002960	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0008653	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0010783	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0012649	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0100520	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0100820	ORPHA:727	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001903	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001933	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002014	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002017	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002027	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002239	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002586	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0002829	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0003326	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0003565	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0004396	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0004936	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0005244	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0012378	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0012614	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0032018	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0032230	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0033505	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0033557	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0033559	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0034104	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0200042	ORPHA:727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000246	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000421	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000554	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0000965	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001369	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001482	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001635	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001701	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001733	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0001824	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0003401	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0008046	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0009830	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0011675	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0025188	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0025420	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0031363	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0100534	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0100749	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:727	Microscopic polyangiitis		HP:0100758	ORPHA:727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0000252	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0000478	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0000504	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0000618	ORPHA:726	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001251	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001252	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001257	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001259	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001263	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001266	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001284	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0001336	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0002069	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0002191	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0002313	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0002376	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0002385	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0007359	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:726	Alpers-Huttenlocher syndrome		HP:0100022	ORPHA:726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0000978	ORPHA:721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0001872	ORPHA:721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0001873	ORPHA:721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0001892	ORPHA:721	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0000140	ORPHA:721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0000421	ORPHA:721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0001744	ORPHA:721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:721	Gray platelet syndrome		HP:0002863	ORPHA:721	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:720	Pili bifurcati		HP:0001595	ORPHA:720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:720	Pili bifurcati		HP:0010719	ORPHA:720	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0001945	ORPHA:723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0002094	ORPHA:723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0011949	ORPHA:723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0012418	ORPHA:723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0020102	ORPHA:723	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0001824	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0002093	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0002202	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0002721	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0002875	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0002878	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0004887	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0006515	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0010702	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0011991	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0025395	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0031246	ORPHA:723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0002664	ORPHA:723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0005948	ORPHA:723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0009098	ORPHA:723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0025435	ORPHA:723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0031863	ORPHA:723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:723	Pneumocystosis		HP:0032177	ORPHA:723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000478	ORPHA:722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000504	ORPHA:722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0040228	ORPHA:722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000212	ORPHA:722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000230	ORPHA:722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000137	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000238	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000370	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000704	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000787	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0000951	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0001305	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0002086	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0002588	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0011027	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:722	Hypoplasminogenemia		HP:0030160	ORPHA:722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002804	ORPHA:562528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0012385	ORPHA:562528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0012758	ORPHA:562528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000205	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000343	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000347	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000431	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000470	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000486	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000494	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000750	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001181	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001193	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001249	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001252	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001263	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001270	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001371	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001762	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002000	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002020	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002793	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0009931	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0011824	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0100790	ORPHA:562528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000160	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000218	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000248	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000252	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000286	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000319	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000337	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000369	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000565	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001250	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001251	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001276	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001848	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002019	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002093	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002307	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0002650	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0004322	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0011968	ORPHA:562528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000256	ORPHA:562528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000316	ORPHA:562528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000400	ORPHA:562528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000417	ORPHA:562528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0000545	ORPHA:562528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562528	Congenital limbs-face contractures-hypotonia-developmental delay syndrome		HP:0001166	ORPHA:562528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001270	ORPHA:435638	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000356	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000448	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000494	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000733	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000750	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001252	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001344	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002002	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0005280	ORPHA:435638	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000175	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000219	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000248	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000286	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000303	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000322	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000341	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000347	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000407	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000463	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000568	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000581	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000729	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0000960	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001182	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001233	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001251	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001629	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001631	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001642	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001643	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001677	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0001845	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002021	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002069	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002121	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002123	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002650	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002705	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0002714	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0003086	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0003202	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0006380	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0006585	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0007018	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0009623	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0010055	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0010663	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0011304	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0012762	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435638	3p25.3 microdeletion syndrome		HP:0100259	ORPHA:435638	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000044	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000135	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000144	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000248	ORPHA:1173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000512	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000639	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000648	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000708	ORPHA:1173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000726	ORPHA:1173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000751	ORPHA:1173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000771	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0000864	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0001251	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0001252	ORPHA:1173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0002167	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0002558	ORPHA:1173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0004209	ORPHA:1173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0004322	ORPHA:1173	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0004374	ORPHA:1173	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1173	Cerebellar ataxia-hypogonadism syndrome		HP:0007703	ORPHA:1173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002069	ORPHA:140927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002266	ORPHA:140927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0011193	ORPHA:140927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0032792	ORPHA:140927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0032807	ORPHA:140927	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0001350	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002018	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002104	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002131	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002172	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002315	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0002321	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0025401	ORPHA:140927	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0001268	ORPHA:140927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:140927	Self-limited neonatal-infantile epilepsy		HP:0031491	ORPHA:140927	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0000407	ORPHA:1171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0000648	ORPHA:1171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0001251	ORPHA:1171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0001284	ORPHA:1171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0001298	ORPHA:1171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0001324	ORPHA:1171	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0000496	ORPHA:1171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0000729	ORPHA:1171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0001250	ORPHA:1171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0001332	ORPHA:1171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0001761	ORPHA:1171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0002015	ORPHA:1171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1171	Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome		HP:0100543	ORPHA:1171	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0000640	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0000750	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001249	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001251	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001260	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001263	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001310	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0002066	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0031936	ORPHA:1170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0000657	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001252	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001272	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001324	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001348	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001763	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0002311	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0002506	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0006855	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0007272	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0100543	ORPHA:1170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0000602	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001257	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0001337	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0002198	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0002280	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0003128	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0004322	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0009830	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1170	Autosomal recessive cerebelloparenchymal disorder type 3		HP:0010794	ORPHA:1170	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488191	Female infertility due to oocyte meiotic arrest		HP:0008222	ORPHA:488191	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:488191	Female infertility due to oocyte meiotic arrest		HP:0031515	ORPHA:488191	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:488191	Female infertility due to oocyte meiotic arrest		HP:0031516	ORPHA:488191	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488191	Female infertility due to oocyte meiotic arrest		HP:0020155	ORPHA:488191	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488191	Female infertility due to oocyte meiotic arrest	NOT	HP:0000147	ORPHA:488191	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:488191	Female infertility due to oocyte meiotic arrest	NOT	HP:0008669	ORPHA:488191	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1179	Benign paroxysmal tonic upgaze of childhood with ataxia		HP:0000496	ORPHA:1179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1179	Benign paroxysmal tonic upgaze of childhood with ataxia		HP:0000639	ORPHA:1179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1179	Benign paroxysmal tonic upgaze of childhood with ataxia		HP:0002131	ORPHA:1179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001249	ORPHA:572798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001263	ORPHA:572798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0008947	ORPHA:572798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0100022	ORPHA:572798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000718	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001250	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001272	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001324	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001347	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001511	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002059	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002119	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002151	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002167	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002342	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001288	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002451	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002509	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002518	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0003128	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0003700	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0008936	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0012379	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0012430	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0012448	ORPHA:572798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000218	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000219	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000316	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000369	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000431	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000510	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000577	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000639	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0000646	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001251	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001310	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001320	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001337	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001344	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001638	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001873	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001998	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0001999	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002015	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002187	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002198	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002305	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002352	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002365	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002421	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0002510	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0003698	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0005656	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0006956	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0007772	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0012704	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		HP:0031165	ORPHA:572798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0000505	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0000510	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0000580	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0000639	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0001251	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0001252	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0001288	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0007360	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1178	Ataxia-tapetoretinal degeneration syndrome		HP:0100543	ORPHA:1178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140933	Linear atrophoderma of Moulin		HP:0007546	ORPHA:140933	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:140933	Linear atrophoderma of Moulin	NOT	HP:0000989	ORPHA:140933	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:140933	Linear atrophoderma of Moulin	NOT	HP:0011123	ORPHA:140933	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:140933	Linear atrophoderma of Moulin	NOT	HP:0030053	ORPHA:140933	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:140933	Linear atrophoderma of Moulin	NOT	HP:0100324	ORPHA:140933	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0000162	ORPHA:718	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0000175	ORPHA:718	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0000347	ORPHA:718	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0001508	ORPHA:718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0001561	ORPHA:718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0002643	ORPHA:718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0002781	ORPHA:718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0008872	ORPHA:718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0012418	ORPHA:718	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0000453	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0000961	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0001601	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0001607	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0001648	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0002015	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0002777	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0002779	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0002780	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0004890	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0010307	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:718	Isolated Pierre Robin sequence		HP:0010535	ORPHA:718	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0002073	ORPHA:1177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0000639	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0001260	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0002015	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0003474	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0006895	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0007083	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0007240	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0007256	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0007350	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0008003	ORPHA:1177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0001761	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0002061	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0002650	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0003115	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0003700	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0007340	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0010794	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0100543	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes		HP:0200101	ORPHA:1177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes	NOT	HP:0000648	ORPHA:1177	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes	NOT	HP:0000819	ORPHA:1177	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes	NOT	HP:0001638	ORPHA:1177	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1177	Early-onset cerebellar ataxia with retained tendon reflexes	NOT	HP:0005775	ORPHA:1177	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002073	ORPHA:1175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0000639	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0001152	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0001270	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0001310	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0001347	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0001761	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002070	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002075	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002080	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002312	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002317	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002359	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002464	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002503	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002650	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0003445	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0003447	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0006855	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0007141	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0007240	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0008944	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0200101	ORPHA:1175	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0002395	ORPHA:1175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0003487	ORPHA:1175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1175	X-linked progressive cerebellar ataxia		HP:0009027	ORPHA:1175	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0000023	ORPHA:1174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0000028	ORPHA:1174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0000325	ORPHA:1174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0000337	ORPHA:1174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0000668	ORPHA:1174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0000691	ORPHA:1174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0001251	ORPHA:1174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0001288	ORPHA:1174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0001761	ORPHA:1174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0002167	ORPHA:1174	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0002213	ORPHA:1174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1174	Cerebellar ataxia-ectodermal dysplasia syndrome		HP:0008070	ORPHA:1174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002239	ORPHA:79076	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002014	ORPHA:79076	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0004326	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002243	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0000256	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001031	ORPHA:79076	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0010797	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001999	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002003	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0000316	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0000494	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0005280	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0000369	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0000160	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0000331	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001256	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0004390	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002027	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002573	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001903	ORPHA:79076	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002249	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0005505	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0003073	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002584	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002576	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002035	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0100759	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001627	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001290	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001270	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001631	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001643	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0004322	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0006608	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001028	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001249	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0001892	ORPHA:79076	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0005227	ORPHA:79076	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0030257	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002007	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0002705	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0011304	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79076	Juvenile polyposis of infancy		HP:0010174	ORPHA:79076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0000750	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0001249	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0001251	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0001263	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0001324	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0001337	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0001878	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0001923	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0002076	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0002904	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0002913	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0003198	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0003201	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0003394	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0003738	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0009020	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0012638	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0020062	ORPHA:713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0000083	ORPHA:713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0000556	ORPHA:713	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:713	Glycogen storage disease due to phosphoglycerate kinase 1 deficiency		HP:0000618	ORPHA:713	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0032351	ORPHA:716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000252	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000708	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000938	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000964	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0001010	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0001250	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0001328	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0002353	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0002500	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0004923	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0010864	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0410021	ORPHA:716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000716	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000726	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000736	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0000739	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0001251	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0001298	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0001337	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0002061	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0030680	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:716	Phenylketonuria		HP:0100704	ORPHA:716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0007734	ORPHA:79078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0010286	ORPHA:79078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0010287	ORPHA:79078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0032300	ORPHA:79078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0011801	ORPHA:79078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0000217	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0000282	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0000315	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0000520	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0000587	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0000629	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0001097	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0001824	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0001945	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0002960	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0003261	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0003324	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0003493	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0003496	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0008049	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0012378	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0032230	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0100540	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0100614	ORPHA:79078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0000618	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0001873	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0001970	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0002716	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0005200	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0005994	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0007807	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0011481	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79078	IgG4-related dacryoadenitis and sialadenitis		HP:0100646	ORPHA:79078	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0001176	ORPHA:276630	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0001182	ORPHA:276630	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000232	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000316	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000445	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000494	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000674	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000677	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000709	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000716	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000767	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0000768	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0001250	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0001252	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0001513	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0002007	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0002650	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0002808	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0004322	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0007302	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:276630	Symptomatic form of Coffin-Lowry syndrome in female carriers		HP:0030680	ORPHA:276630	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0100595	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003323	ORPHA:715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003236	ORPHA:715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003326	ORPHA:715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003458	ORPHA:715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003546	ORPHA:715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0009051	ORPHA:715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0012378	ORPHA:715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:6000198	ORPHA:715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0001265	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0001288	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0002913	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003202	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003391	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003394	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:715	Glycogen storage disease due to muscle phosphorylase kinase deficiency		HP:0003551	ORPHA:715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000194	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000218	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000262	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000303	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000316	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000322	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000324	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000348	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000431	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000470	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0000508	ORPHA:710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0001156	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0001385	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0003307	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0004209	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0004322	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0005048	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0006101	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0009773	ORPHA:710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0010669	ORPHA:710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0011304	ORPHA:710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:710	Pfeiffer syndrome		HP:0012368	ORPHA:710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0000952	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0001744	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0001923	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0001930	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0002240	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0003568	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0008282	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0025435	ORPHA:712	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0001082	ORPHA:712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0001249	ORPHA:712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0001789	ORPHA:712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0004447	ORPHA:712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:712	Hemolytic anemia due to glucophosphate isomerase deficiency		HP:0011981	ORPHA:712	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0001171	ORPHA:2492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0001622	ORPHA:2492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0001626	ORPHA:2492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0002093	ORPHA:2492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0002991	ORPHA:2492	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0002992	ORPHA:2492	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0004050	ORPHA:2492	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0004322	ORPHA:2492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0006101	ORPHA:2492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2492	FATCO syndrome		HP:0008368	ORPHA:2492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1160	Chylous ascites		HP:0000501	ORPHA:1160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1160	Chylous ascites		HP:0001004	ORPHA:1160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1160	Chylous ascites		HP:0001482	ORPHA:1160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1160	Chylous ascites		HP:0001541	ORPHA:1160	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1160	Chylous ascites		HP:0001733	ORPHA:1160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1160	Chylous ascites		HP:0002242	ORPHA:1160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1160	Chylous ascites		HP:0002664	ORPHA:1160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0000252	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0000486	ORPHA:2491	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0000821	ORPHA:2491	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0001162	ORPHA:2491	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0001171	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0002983	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0003019	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0003762	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0004322	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0005792	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0006495	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0007477	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0008736	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2491	Müllerian duct anomalies-limb anomalies syndrome		HP:0009811	ORPHA:2491	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1168	Ataxia-oculomotor apraxia type 1		HP:0000707	ORPHA:1168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1168	Ataxia-oculomotor apraxia type 1		HP:0001251	ORPHA:1168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1168	Ataxia-oculomotor apraxia type 1		HP:0001288	ORPHA:1168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1168	Ataxia-oculomotor apraxia type 1		HP:0009830	ORPHA:1168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1168	Ataxia-oculomotor apraxia type 1		HP:0010747	ORPHA:1168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0000468	ORPHA:435660	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0000855	ORPHA:435660	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0003635	ORPHA:435660	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0009125	ORPHA:435660	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0000147	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0000831	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0000876	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0000956	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0001397	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0002155	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0002240	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0003236	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0003292	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0003712	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0008993	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0009017	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0012881	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0030685	ORPHA:435660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0008994	ORPHA:435660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435660	LIPE-related familial partial lipodystrophy		HP:0008997	ORPHA:435660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2499	Metachondromatosis		HP:0000944	ORPHA:2499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2499	Metachondromatosis		HP:0002653	ORPHA:2499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2499	Metachondromatosis		HP:0005701	ORPHA:2499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2499	Metachondromatosis		HP:0005930	ORPHA:2499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2499	Metachondromatosis		HP:0006824	ORPHA:2499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2499	Metachondromatosis		HP:0010885	ORPHA:2499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2499	Metachondromatosis		HP:0100777	ORPHA:2499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140966	Palmoplantar keratoderma, Nagashima type		HP:0000975	ORPHA:140966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140966	Palmoplantar keratoderma, Nagashima type		HP:0000982	ORPHA:140966	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000178	ORPHA:1166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0011333	ORPHA:1166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000028	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000076	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000175	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000252	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000347	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000411	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0000776	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0001276	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0001387	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0002093	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0002120	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0004322	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0005562	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0008678	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0009804	ORPHA:1166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0001263	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0001629	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0001636	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0001679	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0002086	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0003272	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0003422	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0004414	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1166	Congenital unilateral hypoplasia of depressor anguli oris		HP:0030680	ORPHA:1166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2497	Upper limb mesomelic dysplasia, type Fryns		HP:0002986	ORPHA:2497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2497	Upper limb mesomelic dysplasia, type Fryns		HP:0003022	ORPHA:2497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2497	Upper limb mesomelic dysplasia, type Fryns		HP:0009465	ORPHA:2497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000347	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000494	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000506	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000508	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0001155	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0001156	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0001387	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0001440	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0001760	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0001773	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0002652	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0002705	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0002983	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0002992	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0003019	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0003027	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0031095	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0004209	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0004322	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0005048	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0005916	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0009465	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0010293	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0100240	ORPHA:2496	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0002823	ORPHA:2496	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000126	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000160	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000190	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000272	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000325	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000343	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000365	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000414	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000444	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000534	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0000545	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0001537	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0002815	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0002857	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0003028	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2496	Mesomelia-synostoses syndrome		HP:0030680	ORPHA:2496	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0001879	ORPHA:1164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002099	ORPHA:1164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002715	ORPHA:1164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0012735	ORPHA:1164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0001824	ORPHA:1164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002110	ORPHA:1164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002120	ORPHA:1164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0011134	ORPHA:1164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0001231	ORPHA:1164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002092	ORPHA:1164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002093	ORPHA:1164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002097	ORPHA:1164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0002105	ORPHA:1164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1164	Allergic bronchopulmonary aspergillosis		HP:0025426	ORPHA:1164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0010997	ORPHA:2495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0011133	ORPHA:2495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0100009	ORPHA:2495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000044	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000141	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000802	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000870	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001250	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0002017	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0002315	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0002920	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0007359	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0008163	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0008214	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0008240	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0008245	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0012658	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0012691	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0030341	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0030344	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0030521	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0040171	ORPHA:2495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000238	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000602	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001067	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001085	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001251	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001269	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001317	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001513	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0002354	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001288	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0002516	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0003484	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0004302	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0004408	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0006824	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0007340	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0007715	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0007924	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0008202	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0008237	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0010628	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0011442	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0011730	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0011750	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0012246	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0012285	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0012505	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0030532	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0030591	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0100010	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0100543	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0100661	ORPHA:2495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000020	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000360	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000520	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000618	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0000712	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001262	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001279	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0001342	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0002167	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0002512	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0003418	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0006520	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0008069	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0010534	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0010828	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0011752	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0030766	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0030878	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0045026	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2495	Meningioma		HP:0100648	ORPHA:2495	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0004295	ORPHA:2494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0005246	ORPHA:2494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0001824	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0002013	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0002018	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0002027	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0003073	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0003075	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0004395	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0005202	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0012398	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0025406	ORPHA:2494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0002014	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0002020	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0002039	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0002239	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0004394	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0004396	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0004840	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0012126	ORPHA:2494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2494	Ménétrier disease		HP:0001907	ORPHA:2494	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0012735	ORPHA:1163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0020153	ORPHA:1163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001875	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001880	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001945	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002105	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002113	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002721	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0006528	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0025179	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0030878	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0032016	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0032177	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0100749	ORPHA:1163	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000077	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000246	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000491	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000505	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000620	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001626	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001742	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002031	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002090	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002094	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002099	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002102	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002206	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002207	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002315	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0003212	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0004377	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0006510	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0006516	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0011355	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0012115	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0020103	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0031417	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0100326	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0200026	ORPHA:1163	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000629	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000772	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0000925	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001250	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001287	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0001297	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002110	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002170	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002202	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002383	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002693	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0002754	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0004302	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0005607	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0011314	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0011450	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1163	Aspergillosis		HP:0011531	ORPHA:1163	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000160	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000174	ORPHA:1150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000201	ORPHA:1150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000233	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000293	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000346	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000347	ORPHA:1150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000364	ORPHA:1150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000366	ORPHA:1150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000358	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0000581	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0001181	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0001231	ORPHA:1150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0001250	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0001252	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0001387	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0001511	ORPHA:1150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0001561	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0002353	ORPHA:1150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0002714	ORPHA:1150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0003043	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0004322	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0010751	ORPHA:1150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1150	Arthrogryposis multiplex congenita-whistling face syndrome		HP:0011344	ORPHA:1150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002353	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002381	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002383	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002435	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002664	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002861	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0003396	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0004936	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0006824	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0006979	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0007360	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0007703	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0008678	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0011972	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0012470	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000989	ORPHA:2481	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000995	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001072	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001249	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001250	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002230	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002516	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002922	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0005603	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0007440	ORPHA:2481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000238	ORPHA:2481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001085	ORPHA:2481	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000009	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000505	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000567	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000603	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000648	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000708	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000709	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0000737	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001268	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001269	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001305	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0001522	ORPHA:2481	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002015	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002119	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002170	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002176	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002269	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002308	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2481	Neurocutaneous melanocytosis		HP:0002315	ORPHA:2481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0000982	ORPHA:87503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0001155	ORPHA:87503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0001760	ORPHA:87503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0007404	ORPHA:87503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0011123	ORPHA:87503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0031190	ORPHA:87503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0000975	ORPHA:87503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0001218	ORPHA:87503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0001371	ORPHA:87503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0007390	ORPHA:87503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0007447	ORPHA:87503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0010783	ORPHA:87503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0025092	ORPHA:87503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0008064	ORPHA:87503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:87503	Mal de Meleda		HP:0031452	ORPHA:87503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0000617	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0001249	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0001251	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0001260	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0001263	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0001272	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0001288	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0002070	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0002078	ORPHA:284271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0000639	ORPHA:284271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0002015	ORPHA:284271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0002317	ORPHA:284271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284271	Autosomal recessive cerebellar ataxia-psychomotor delay syndrome		HP:0007979	ORPHA:284271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000394	ORPHA:140952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0001770	ORPHA:140952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0002023	ORPHA:140952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0004209	ORPHA:140952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0004322	ORPHA:140952	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000066	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000076	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000083	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000085	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000086	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000104	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000219	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000414	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000431	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000506	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000813	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0001671	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0008665	ORPHA:140952	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000545	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000556	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0000625	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0001250	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0001659	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0002984	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0003396	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0004415	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0007754	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140952	Syndactyly-telecanthus-anogenital and renal malformations syndrome		HP:0011560	ORPHA:140952	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0003635	ORPHA:435651	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0009125	ORPHA:435651	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0000147	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0000831	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0000876	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0000956	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0001397	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0001733	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0002155	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0002240	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0003292	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0003712	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0008981	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0009017	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy		HP:0030685	ORPHA:435651	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:435651	CIDEC-related familial partial lipodystrophy	NOT	HP:0000292	ORPHA:435651	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0000926	ORPHA:1159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0001386	ORPHA:1159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002515	ORPHA:1159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002655	ORPHA:1159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0003301	ORPHA:1159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0004267	ORPHA:1159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0005195	ORPHA:1159	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0001225	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0001324	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0001376	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0001384	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002650	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002815	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002829	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0003388	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0003423	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0004322	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0004582	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0004603	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0006256	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0008422	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0009473	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0009811	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0011406	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0012385	ORPHA:1159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0000464	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002812	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002857	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002867	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0002970	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0003043	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0003307	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0003370	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0003371	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0004568	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0006247	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0006429	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0008833	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0010580	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0025477	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0040160	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia		HP:0100864	ORPHA:1159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia	NOT	HP:0002923	ORPHA:1159	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia	NOT	HP:0025021	ORPHA:1159	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1159	Progressive pseudorheumatoid dysplasia	NOT	HP:0032436	ORPHA:1159	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0000365	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0000567	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0001263	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0001511	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0002750	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0009738	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0009739	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0009778	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0010049	ORPHA:2489	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0000028	ORPHA:2489	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0000286	ORPHA:2489	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2489	Upper limb defect-eye and ear abnormalities syndrome		HP:0000518	ORPHA:2489	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0000047	ORPHA:2487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0030680	ORPHA:2487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0000069	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0000358	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0000400	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0000470	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0000960	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0001622	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0001743	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0002093	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0002992	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2487	Lower limb malformation-hypospadias syndrome		HP:0100559	ORPHA:2487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0002015	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0410151	ORPHA:411696	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0100633	ORPHA:411696	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0002020	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0002013	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0011968	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0002027	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0030914	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0500093	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0004789	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0410328	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0001025	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0500095	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0002099	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0003193	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0001047	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0410227	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0000737	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0008872	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0001508	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0002018	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0410019	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0100749	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0031984	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0031985	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0031858	ORPHA:411696	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0010450	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0410152	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411696	Proton-pump inhibitor-responsive esophageal eosinophilia		HP:0002032	ORPHA:411696	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000023	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000325	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000400	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000490	ORPHA:1154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000505	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000508	ORPHA:1154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000512	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000602	ORPHA:1154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000648	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0000767	ORPHA:1154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0001166	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0001387	ORPHA:1154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0001776	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0004097	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0005879	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0010489	ORPHA:1154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1154	Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome		HP:0010751	ORPHA:1154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0000924	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0001004	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0001387	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0001508	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0002652	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0002653	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0002829	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0003202	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0006824	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0011001	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0011987	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0100774	ORPHA:2485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0100559	ORPHA:2485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0100560	ORPHA:2485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0000987	ORPHA:2485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0001369	ORPHA:2485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2485	Melorheostosis		HP:0100784	ORPHA:2485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000270	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000316	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000336	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000347	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000520	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000774	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000944	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0003103	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0004322	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0006487	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0010306	ORPHA:2484	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000076	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000126	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000293	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000324	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000365	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000684	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000692	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000772	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0000894	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0001671	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0002007	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0002205	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0002650	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0002673	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0002827	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0002879	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0003172	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0004493	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0001382	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0009771	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0009882	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0010230	ORPHA:2484	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0001539	ORPHA:2484	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2484	Melnick-Needles syndrome		HP:0002093	ORPHA:2484	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0000298	ORPHA:2483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0000969	ORPHA:2483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0006824	ORPHA:2483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0010471	ORPHA:2483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0011123	ORPHA:2483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0100539	ORPHA:2483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0100825	ORPHA:2483	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0000158	ORPHA:2483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0000221	ORPHA:2483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0010628	ORPHA:2483	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0000639	ORPHA:2483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0001945	ORPHA:2483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0002716	ORPHA:2483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2483	Melkersson-Rosenthal syndrome		HP:0012332	ORPHA:2483	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002202	ORPHA:50251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0000765	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0001824	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002094	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002098	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002103	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0012735	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0025142	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0100749	ORPHA:50251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002015	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002088	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002240	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002716	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0002795	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0007011	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0011025	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:50251	Pleural mesothelioma		HP:0031041	ORPHA:50251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0002073	ORPHA:284289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0012379	ORPHA:284289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0000508	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0000608	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0000641	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001152	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001260	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001272	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001310	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001347	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001348	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001350	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001761	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0002070	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0002078	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0002197	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0002380	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0003457	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0007240	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0008969	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0010545	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0011448	ORPHA:284289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0000503	ORPHA:284289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0000518	ORPHA:284289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0000651	ORPHA:284289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0000666	ORPHA:284289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0001256	ORPHA:284289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284289	Adult-onset autosomal recessive cerebellar ataxia		HP:0002080	ORPHA:284289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000336	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000400	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000411	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000448	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000486	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000664	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0001249	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0002650	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0002808	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0004322	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0010318	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0010807	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0030680	ORPHA:2471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000028	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000174	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000303	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000316	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000322	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000347	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000358	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000430	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000508	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000689	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0000767	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0004326	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0007598	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2471	McDonough syndrome		HP:0012745	ORPHA:2471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000528	ORPHA:2470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000568	ORPHA:2470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0001249	ORPHA:2470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000776	ORPHA:2470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0002088	ORPHA:2470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0002089	ORPHA:2470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0030680	ORPHA:2470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000028	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000076	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000085	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000089	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000130	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0000369	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0001252	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0001508	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0001511	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0001734	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0025408	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0100800	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2470	Matthew-Wood syndrome		HP:0100867	ORPHA:2470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0000639	ORPHA:284282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0000750	ORPHA:284282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0001260	ORPHA:284282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0001265	ORPHA:284282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0001270	ORPHA:284282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0002066	ORPHA:284282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0002070	ORPHA:284282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284282	Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency		HP:0002839	ORPHA:284282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000194	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000218	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000232	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000252	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000256	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000286	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000316	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000322	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000347	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000407	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000411	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000431	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000483	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000485	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000494	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000545	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000593	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000639	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000733	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000821	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0000938	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0001182	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0001249	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0001250	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0001251	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0001252	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0001263	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0002007	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0002167	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0002353	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0002650	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0002808	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0002970	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0003124	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0004322	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0001382	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0007676	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0009891	ORPHA:2479	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0010508	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0010978	ORPHA:2479	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2479	Megalocornea-intellectual disability syndrome		HP:0100693	ORPHA:2479	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0000218	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0000275	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0000347	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0000411	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0000431	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0000465	ORPHA:1147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0000470	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0001181	ORPHA:1147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0001387	ORPHA:1147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0002650	ORPHA:1147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0003049	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0003272	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0003422	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0004322	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0006501	ORPHA:1147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0007598	ORPHA:1147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0008368	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0009465	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0010557	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1147	Sheldon-Hall syndrome		HP:0100830	ORPHA:1147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0000708	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0001250	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0001251	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0001257	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0001268	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0002317	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0002333	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0005490	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0007341	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:6000461	ORPHA:2478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0000717	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0001249	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0001332	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0002071	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0002133	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0002305	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0002312	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2478	Megalencephalic leukoencephalopathy with subcortical cysts		HP:0012762	ORPHA:2478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0000160	ORPHA:1146	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0001181	ORPHA:1146	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0001387	ORPHA:1146	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0001838	ORPHA:1146	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0001883	ORPHA:1146	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0003272	ORPHA:1146	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0009465	ORPHA:1146	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0010557	ORPHA:1146	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1146	Distal arthrogryposis type 1		HP:0100490	ORPHA:1146	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000040	ORPHA:2477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000053	ORPHA:2477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000235	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000256	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000268	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000269	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000307	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000431	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000470	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0000490	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0001249	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0001631	ORPHA:2477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0001956	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0002007	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0002750	ORPHA:2477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2477	Isolated megalencephaly		HP:0002857	ORPHA:2477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0000175	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0001543	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0001629	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0002323	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0002414	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0004383	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0004397	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0006501	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2476	Dysraphism-cleft lip/palate-limb reduction defects syndrome		HP:0100335	ORPHA:2476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0001284	ORPHA:1145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002033	ORPHA:1145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002398	ORPHA:1145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0003202	ORPHA:1145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0003445	ORPHA:1145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0004303	ORPHA:1145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0006802	ORPHA:1145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0000218	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0000773	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0000887	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0001220	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002058	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002093	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002098	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002425	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002804	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002987	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0003273	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0003701	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0006380	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0006466	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0007269	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0008947	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0009071	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0020110	ORPHA:1145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0000028	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0001290	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0001308	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002009	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002460	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002518	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0002751	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0003324	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0007178	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0008180	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0030319	ORPHA:1145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1145	Infantile-onset X-linked spinal muscular atrophy		HP:0100543	ORPHA:1145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1144	Arthrogryposis-like hand anomaly-sensorineural deafness syndrome		HP:0000407	ORPHA:1144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1144	Arthrogryposis-like hand anomaly-sensorineural deafness syndrome		HP:0001166	ORPHA:1144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1144	Arthrogryposis-like hand anomaly-sensorineural deafness syndrome		HP:0001387	ORPHA:1144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1144	Arthrogryposis-like hand anomaly-sensorineural deafness syndrome		HP:0004322	ORPHA:1144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1144	Arthrogryposis-like hand anomaly-sensorineural deafness syndrome		HP:0004326	ORPHA:1144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000174	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000268	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000286	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000316	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000358	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000486	ORPHA:2475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000545	ORPHA:2475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000592	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000772	ORPHA:2475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0000912	ORPHA:2475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0001631	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0002002	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0002086	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0002211	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0002750	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0003298	ORPHA:2475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0004209	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0001382	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2475	White forelock with malformations		HP:0006101	ORPHA:2475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0001015	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0001528	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0006496	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0012721	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0025104	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0040064	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0100555	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0100585	ORPHA:75508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0000969	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0002753	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0002984	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0003022	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0004936	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0005792	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0010484	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0011804	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0100671	ORPHA:75508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0001155	ORPHA:75508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0001760	ORPHA:75508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0003401	ORPHA:75508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:75508	Angioosteohypotrophic syndrome		HP:0009824	ORPHA:75508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001371	ORPHA:1143	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0003444	ORPHA:1143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001239	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001284	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0002987	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0003202	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0003484	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0006380	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0006466	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0007340	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0008180	ORPHA:1143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0000316	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0000347	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001357	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001558	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001562	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001623	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001627	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0001838	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0002058	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0002098	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0002380	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0002650	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0002747	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0002827	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0003273	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0007477	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0008110	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0008807	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0010781	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0011968	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0030799	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1143	Neurogenic arthrogryposis multiplex congenita		HP:0410263	ORPHA:1143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0030010	ORPHA:2473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0000028	ORPHA:2473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0000126	ORPHA:2473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0000807	ORPHA:2473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001162	ORPHA:2473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0100779	ORPHA:2473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0000003	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0000175	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0000218	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001156	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001249	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001263	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001508	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001629	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001631	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001636	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001643	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0001830	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0002023	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0002251	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0004322	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0004383	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0004397	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0005916	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0006101	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0008368	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0012227	ORPHA:2473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2473	McKusick-Kaufman syndrome		HP:0008678	ORPHA:2473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0000889	ORPHA:1149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0000995	ORPHA:1149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0001288	ORPHA:1149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0001315	ORPHA:1149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0001387	ORPHA:1149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0001883	ORPHA:1149	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0002650	ORPHA:1149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0003312	ORPHA:1149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0006498	ORPHA:1149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1149	Kuskokwim syndrome		HP:0006501	ORPHA:1149	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0001347	ORPHA:100993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0002061	ORPHA:100993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0002314	ORPHA:100993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0001288	ORPHA:100993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0007020	ORPHA:100993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0007340	ORPHA:100993	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0000012	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0000020	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0002064	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0002070	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0002166	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0002169	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0003394	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0003487	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0007210	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0001761	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0010831	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0030014	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0040307	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0100561	ORPHA:100993	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0002607	ORPHA:100993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12		HP:0007350	ORPHA:100993	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12	NOT	HP:0001250	ORPHA:100993	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12	NOT	HP:0002921	ORPHA:100993	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12	NOT	HP:0003457	ORPHA:100993	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100993	Autosomal dominant spastic paraplegia type 12	NOT	HP:0012898	ORPHA:100993	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0001258	ORPHA:100994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0002839	ORPHA:100994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0000020	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0001347	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0002061	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0002064	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0002166	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0003487	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0007256	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0007340	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0007350	ORPHA:100994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0000012	ORPHA:100994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0001761	ORPHA:100994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0002650	ORPHA:100994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0000365	ORPHA:100994	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100994	Autosomal dominant spastic paraplegia type 13		HP:0000510	ORPHA:100994	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100995	Autosomal recessive spastic paraplegia type 14		HP:0001256	ORPHA:100995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100995	Autosomal recessive spastic paraplegia type 14		HP:0001347	ORPHA:100995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100995	Autosomal recessive spastic paraplegia type 14		HP:0001761	ORPHA:100995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100995	Autosomal recessive spastic paraplegia type 14		HP:0002064	ORPHA:100995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100995	Autosomal recessive spastic paraplegia type 14		HP:0003487	ORPHA:100995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100995	Autosomal recessive spastic paraplegia type 14		HP:0006895	ORPHA:100995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100995	Autosomal recessive spastic paraplegia type 14		HP:0007002	ORPHA:100995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0002061	ORPHA:100991	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0002395	ORPHA:100991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0003487	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0007141	ORPHA:100991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0009129	ORPHA:100991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0002342	ORPHA:100991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0001300	ORPHA:100991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0000365	ORPHA:100991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0000510	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0002936	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0003477	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0008944	ORPHA:100991	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0100543	ORPHA:100991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0031958	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0011448	ORPHA:100991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0003401	ORPHA:100991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0001761	ORPHA:100991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0006986	ORPHA:100991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0002650	ORPHA:100991	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0002493	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0006886	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0007350	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0000012	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0002619	ORPHA:100991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0005679	ORPHA:100991	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0008969	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0007340	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100991	Autosomal dominant spastic paraplegia type 10		HP:0005340	ORPHA:100991	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0001833	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0003083	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0004691	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0005280	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0006236	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0006487	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0034391	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0034392	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000126	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000160	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000347	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000365	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000430	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000647	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000678	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000750	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0001363	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0001762	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0004411	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0006633	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0008744	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0009929	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0030084	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0034671	ORPHA:2460	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000232	ORPHA:2460	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000272	ORPHA:2460	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000581	ORPHA:2460	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0001166	ORPHA:2460	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0012385	ORPHA:2460	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000218	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000324	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000325	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000411	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000460	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000494	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000883	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0000895	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2460	Van den Ende-Gupta syndrome		HP:0001822	ORPHA:2460	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002079	ORPHA:100996	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0000009	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0000580	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0000639	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001249	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001257	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001258	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001260	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001288	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001317	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001324	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002061	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002071	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002395	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002500	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0003477	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0003484	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0003487	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0006986	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0007024	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0007108	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0008969	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0012045	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0030506	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0030892	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0100543	ORPHA:100996	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0000496	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0000708	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0000726	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0000819	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001152	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001250	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001328	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0001761	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002145	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002378	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0002495	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100996	Autosomal recessive spastic paraplegia type 15		HP:0003693	ORPHA:100996	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0002395	ORPHA:320411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0003487	ORPHA:320411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0001263	ORPHA:320411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0002064	ORPHA:320411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0002317	ORPHA:320411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0030051	ORPHA:320411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0001249	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0001258	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0001332	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0002079	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0002453	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0002500	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0003477	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:320411	Autosomal recessive spastic paraplegia type 56		HP:0100543	ORPHA:320411	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0000009	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0000572	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0000639	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0001256	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0001270	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0001844	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0002427	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0002445	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100997	X-linked spastic paraplegia type 16		HP:0012719	ORPHA:100997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0001347	ORPHA:100998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0001436	ORPHA:100998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0002064	ORPHA:100998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0003487	ORPHA:100998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0009027	ORPHA:100998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0009130	ORPHA:100998	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0001171	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0001763	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0002174	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0002936	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0003693	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0030237	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0030838	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0030839	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0031374	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100998	Autosomal dominant spastic paraplegia type 17		HP:0040131	ORPHA:100998	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0002169	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0003394	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0007210	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0010831	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0012898	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0030014	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0040307	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0100561	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0000012	ORPHA:100999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0001347	ORPHA:100999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0002061	ORPHA:100999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0002314	ORPHA:100999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0003487	ORPHA:100999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0007020	ORPHA:100999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0007340	ORPHA:100999	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0002070	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0002166	ORPHA:100999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0002064	ORPHA:100999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0001288	ORPHA:100999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0007350	ORPHA:100999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19		HP:0001761	ORPHA:100999	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19	NOT	HP:0001250	ORPHA:100999	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19	NOT	HP:0002921	ORPHA:100999	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100999	Autosomal dominant spastic paraplegia type 19	NOT	HP:0003457	ORPHA:100999	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0000750	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0001249	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0001188	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0001258	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0001274	ORPHA:2466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0001288	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0001347	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0002119	ORPHA:2466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0002381	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0004209	ORPHA:2466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0004322	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0004374	ORPHA:2466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2466	MASA syndrome		HP:0100490	ORPHA:2466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000090	ORPHA:140976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000508	ORPHA:140976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000510	ORPHA:140976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000924	ORPHA:140976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0001392	ORPHA:140976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0040075	ORPHA:140976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000002	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000003	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000365	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000490	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000938	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0000946	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0002652	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0002750	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0003170	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0006824	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0006897	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0010585	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140976	RHYNS syndrome		HP:0011314	ORPHA:140976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0000316	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0000430	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0000568	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0000625	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0002006	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0002098	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0004122	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0004646	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0005273	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0008551	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0009935	ORPHA:1134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1134	Isolated arrhinia		HP:0009927	ORPHA:1134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0000069	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0000160	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0000303	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0000319	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0000358	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0000582	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0000682	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0001156	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0001511	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0001744	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0002231	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0002240	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0002644	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0002650	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0004322	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0004326	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0004493	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0004828	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0005105	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0005978	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0006288	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0009912	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0010311	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0100578	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0100651	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1133	AREDYLD syndrome		HP:0100840	ORPHA:1133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000098	ORPHA:2463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001263	ORPHA:2463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001382	ORPHA:2463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001519	ORPHA:2463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0003100	ORPHA:2463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0003782	ORPHA:2463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0012771	ORPHA:2463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000160	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000218	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000268	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000272	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000280	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000316	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000400	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000445	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000767	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000883	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000938	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001166	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001252	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001833	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0003393	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0006086	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0008050	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0008078	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0009004	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0009929	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0010487	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0011822	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0011849	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0012157	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0012368	ORPHA:2463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000289	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000565	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000664	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0000777	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001007	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0001640	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0002162	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0002750	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0008439	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0009002	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2463	Marfanoid habitus-autosomal recessive intellectual disability syndrome		HP:0100579	ORPHA:2463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000028	ORPHA:1131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000218	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000252	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000286	ORPHA:1131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000324	ORPHA:1131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000325	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000347	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000358	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000405	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000407	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000411	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000426	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000465	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000494	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000508	ORPHA:1131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0000767	ORPHA:1131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0001633	ORPHA:1131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0001642	ORPHA:1131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0004322	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0004414	ORPHA:1131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0009794	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0010669	ORPHA:1131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0100555	ORPHA:1131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1131	X-linked mandibulofacial dysostosis		HP:0100840	ORPHA:1131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000268	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000278	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000316	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000347	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000358	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000369	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000494	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000506	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000520	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001166	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001249	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001252	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001763	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002705	ORPHA:2462	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000023	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000327	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000348	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000486	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000508	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000767	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000768	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001334	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001363	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001537	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001634	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001646	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001653	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002007	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002650	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001382	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0100490	ORPHA:2462	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000028	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000252	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000405	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000411	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000463	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000545	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000774	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000921	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000938	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000944	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0000974	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001387	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0001508	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002020	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002104	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002119	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002308	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0002857	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0003042	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0003312	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0006487	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2462	Shprintzen-Goldberg syndrome		HP:0010318	ORPHA:2462	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000160	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000175	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000176	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000193	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000252	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000278	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000298	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000347	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000358	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000369	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000508	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000581	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001166	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001249	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001252	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001263	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001328	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001387	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001460	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001508	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001510	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0002804	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0002974	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0003202	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0003510	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0003560	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0011968	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0012745	ORPHA:2461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000767	ORPHA:2461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000768	ORPHA:2461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001511	ORPHA:2461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0002650	ORPHA:2461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0002808	ORPHA:2461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0007018	ORPHA:2461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0100490	ORPHA:2461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000003	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000036	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000039	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000047	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000072	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000077	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000079	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000104	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000110	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000126	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0000238	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001274	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001321	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001331	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001629	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001651	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001696	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001840	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0001883	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0002021	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0002334	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0003312	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0004307	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0008678	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0010935	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2461	Marden-Walker syndrome		HP:0030680	ORPHA:2461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0002061	ORPHA:100984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0002395	ORPHA:100984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0003487	ORPHA:100984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0009053	ORPHA:100984	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0001288	ORPHA:100984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0002064	ORPHA:100984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0008944	ORPHA:100984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0011448	ORPHA:100984	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0000012	ORPHA:100984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0001270	ORPHA:100984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0002495	ORPHA:100984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0009830	ORPHA:100984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0030051	ORPHA:100984	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0001260	ORPHA:100984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0001510	ORPHA:100984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0002063	ORPHA:100984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0002067	ORPHA:100984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0002359	ORPHA:100984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0006895	ORPHA:100984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100984	Autosomal dominant spastic paraplegia type 3		HP:0100963	ORPHA:100984	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001249	ORPHA:530983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001263	ORPHA:530983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001328	ORPHA:530983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001999	ORPHA:530983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0031936	ORPHA:530983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000486	ORPHA:530983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000750	ORPHA:530983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001252	ORPHA:530983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001256	ORPHA:530983	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000252	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000276	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000286	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000331	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000347	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000455	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000648	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000729	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000733	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000752	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001250	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001251	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001530	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0002493	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0002650	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0002949	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0011968	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0012433	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0012471	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0025160	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0040195	ORPHA:530983	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0000646	ORPHA:530983	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0001385	ORPHA:530983	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0002942	ORPHA:530983	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:530983	Lamb-Shaffer syndrome		HP:0100704	ORPHA:530983	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001072	ORPHA:90291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002829	ORPHA:90291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0003326	ORPHA:90291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0003493	ORPHA:90291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0011024	ORPHA:90291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0030880	ORPHA:90291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0031359	ORPHA:90291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0000077	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0000160	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001009	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001232	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001324	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001386	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002031	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002206	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0003236	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0005590	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0006121	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0006261	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0006530	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0007400	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0011838	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0012531	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0025131	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0025520	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0030859	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0030873	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0031293	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0031917	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0033038	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0033394	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0033560	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034078	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034079	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034080	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034081	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034082	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034083	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034085	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034086	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034087	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034088	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034089	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034090	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034091	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034093	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034094	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034095	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0034117	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:4000170	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:4000171	ORPHA:90291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0000083	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0000093	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0000099	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0000966	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0000989	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001279	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001369	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001371	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001581	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001596	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001701	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001708	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0001919	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002015	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002020	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002092	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002094	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002244	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002250	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002577	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002578	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002584	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002604	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002607	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002617	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0002754	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0009771	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0011799	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0012185	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0012592	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0012622	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0012819	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0031329	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0100580	ORPHA:90291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90291	Systemic sclerosis		HP:0100758	ORPHA:90291	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0001347	ORPHA:100989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0002061	ORPHA:100989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0002314	ORPHA:100989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0001288	ORPHA:100989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0003487	ORPHA:100989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0007020	ORPHA:100989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0000012	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0000020	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0002064	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0002070	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0002166	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0002406	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0003394	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0007340	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0001761	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0009049	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0100561	ORPHA:100989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0002169	ORPHA:100989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8		HP:0006986	ORPHA:100989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8	NOT	HP:0002921	ORPHA:100989	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8	NOT	HP:0003457	ORPHA:100989	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100989	Autosomal dominant spastic paraplegia type 8	NOT	HP:0012898	ORPHA:100989	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000505	ORPHA:67036	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000648	ORPHA:67036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0007663	ORPHA:67036	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000518	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000603	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000639	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0001251	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0001272	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0001284	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0002174	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0002317	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0002522	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0003394	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0003401	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0003474	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0010924	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0012531	ORPHA:67036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000552	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000618	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0000642	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0001172	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0001315	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0001377	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0001761	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0002322	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0002403	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0003438	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0006248	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0007076	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0007787	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0007795	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0007976	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0009468	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0010522	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67036	Autosomal dominant optic atrophy and cataract		HP:0010923	ORPHA:67036	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0000012	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0001257	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0001348	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0002061	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0003487	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0004302	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0006938	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0007340	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0008969	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0011448	ORPHA:100985	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0001260	ORPHA:100985	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0001761	ORPHA:100985	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0002839	ORPHA:100985	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0003693	ORPHA:100985	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0007350	ORPHA:100985	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0100543	ORPHA:100985	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0001249	ORPHA:100985	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0001250	ORPHA:100985	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100985	Autosomal dominant spastic paraplegia type 4		HP:0001251	ORPHA:100985	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0001258	ORPHA:100986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0002061	ORPHA:100986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0002495	ORPHA:100986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0003487	ORPHA:100986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0007340	ORPHA:100986	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0000079	ORPHA:100986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0001317	ORPHA:100986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0001761	ORPHA:100986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0002500	ORPHA:100986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0007210	ORPHA:100986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0011448	ORPHA:100986	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0002070	ORPHA:100986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0002078	ORPHA:100986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0006827	ORPHA:100986	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0000407	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0000518	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0000639	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0001260	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0001271	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0002015	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0002650	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0003484	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0006986	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100986	Autosomal recessive spastic paraplegia type 5A		HP:0009129	ORPHA:100986	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0001258	ORPHA:100988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0001288	ORPHA:100988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0002061	ORPHA:100988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0002395	ORPHA:100988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0002495	ORPHA:100988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0003487	ORPHA:100988	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0001761	ORPHA:100988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0002069	ORPHA:100988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0003202	ORPHA:100988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0008800	ORPHA:100988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0010505	ORPHA:100988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0000020	ORPHA:100988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100988	Autosomal dominant spastic paraplegia type 6		HP:0002174	ORPHA:100988	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000262	ORPHA:93317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000772	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000774	ORPHA:93317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000782	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0000926	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001274	ORPHA:93317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001290	ORPHA:93317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001302	ORPHA:93317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001321	ORPHA:93317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0001678	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0002093	ORPHA:93317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0002657	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0002750	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003085	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0003498	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0004279	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0004991	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0005616	ORPHA:93317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0005871	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0006543	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0008786	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0010049	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0010579	ORPHA:93317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0011675	ORPHA:93317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type		HP:0012819	ORPHA:93317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000218	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000293	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000347	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000460	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000468	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000842	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000855	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000963	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0001000	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0003635	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0005781	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0100578	ORPHA:2457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000270	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000678	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000685	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000831	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000894	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0000956	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0001090	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0001596	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0001804	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0001870	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0001952	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0002155	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0003124	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0003809	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0008070	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0008897	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0008993	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0009003	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0009839	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0011334	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0030781	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2457	Mandibuloacral dysplasia		HP:0030809	ORPHA:2457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2456	Familial supernumerary nipples		HP:0000119	ORPHA:2456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2456	Familial supernumerary nipples		HP:0002558	ORPHA:2456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0000657	ORPHA:1125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0001251	ORPHA:1125	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0000750	ORPHA:1125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0001151	ORPHA:1125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0001270	ORPHA:1125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0001328	ORPHA:1125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0002419	ORPHA:1125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0006817	ORPHA:1125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0006961	ORPHA:1125	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0000486	ORPHA:1125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0000639	ORPHA:1125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0001249	ORPHA:1125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0001250	ORPHA:1125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0001252	ORPHA:1125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1125	Ocular motor apraxia, Cogan type		HP:0002312	ORPHA:1125	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002812	ORPHA:93315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0003025	ORPHA:93315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0003300	ORPHA:93315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0003468	ORPHA:93315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0003908	ORPHA:93315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0004322	ORPHA:93315	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000768	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0001376	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002650	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002857	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002970	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0003026	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0003521	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0006385	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0009763	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0009824	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0011849	ORPHA:93315	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000218	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000307	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000324	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000358	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000384	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000385	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000411	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000505	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000520	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000545	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000926	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002938	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002945	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002948	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002982	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0004586	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0004625	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0008417	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0008422	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0008577	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0009896	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0012368	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0100559	ORPHA:93315	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000164	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000470	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0000486	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0001891	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002659	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0002866	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0004349	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0005743	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0007906	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0008440	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0009882	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0030084	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0031427	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93315	Spondylometaphyseal dysplasia, 'corner fracture' type		HP:0032208	ORPHA:93315	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1123	Caudal appendage-deafness syndrome		HP:0000028	ORPHA:1123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1123	Caudal appendage-deafness syndrome		HP:0001249	ORPHA:1123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1123	Caudal appendage-deafness syndrome		HP:0001999	ORPHA:1123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1123	Caudal appendage-deafness syndrome		HP:0002825	ORPHA:1123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1123	Caudal appendage-deafness syndrome		HP:0004322	ORPHA:1123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1123	Caudal appendage-deafness syndrome		HP:0008610	ORPHA:1123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1123	Caudal appendage-deafness syndrome		HP:0011297	ORPHA:1123	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0000925	ORPHA:93316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0000944	ORPHA:93316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0100255	ORPHA:93316	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0000926	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0001385	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002650	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002812	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002815	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002857	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002867	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0003375	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0003510	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0003521	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0010574	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0100866	ORPHA:93316	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0000185	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0000347	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0000402	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0000545	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0001561	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002020	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002033	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0002751	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0003019	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0003026	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0003796	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0008833	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0011470	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0011471	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93316	Spondylometaphyseal dysplasia, Schmidt type		HP:0100864	ORPHA:93316	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1122	Ulnar hypoplasia-split foot syndrome		HP:0001171	ORPHA:1122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1122	Ulnar hypoplasia-split foot syndrome		HP:0001839	ORPHA:1122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1122	Ulnar hypoplasia-split foot syndrome		HP:0003022	ORPHA:1122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1122	Ulnar hypoplasia-split foot syndrome		HP:0006501	ORPHA:1122	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0000772	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0000776	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001172	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001177	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001199	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001250	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001522	ORPHA:1120	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001631	ORPHA:1120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001643	ORPHA:1120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001646	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001647	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001680	ORPHA:1120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0001772	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0002093	ORPHA:1120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0002101	ORPHA:1120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0002119	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0002414	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0003422	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0005180	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0006695	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0006703	ORPHA:1120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0007598	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0009623	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0009778	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0009882	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0010772	ORPHA:1120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1120	Lung agenesis-heart defect-thumb anomalies syndrome		HP:0011039	ORPHA:1120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0000992	ORPHA:90283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0025474	ORPHA:90283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0031191	ORPHA:90283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0003493	ORPHA:90283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0025528	ORPHA:90283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0030057	ORPHA:90283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0030351	ORPHA:90283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0032235	ORPHA:90283	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus		HP:0020151	ORPHA:90283	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus	NOT	HP:0007483	ORPHA:90283	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus	NOT	HP:0040189	ORPHA:90283	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:90283	Lupus erythematosus tumidus	NOT	HP:0100699	ORPHA:90283	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0000270	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0000347	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0000494	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0000586	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0001166	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0001249	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0001263	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0002007	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0003196	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0008947	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0010539	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0010565	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0011800	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0011968	ORPHA:1129	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1129	Arachnodactyly-abnormal ossification-intellectual disability syndrome		HP:0002104	ORPHA:1129	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000925	ORPHA:93314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000926	ORPHA:93314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001510	ORPHA:93314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002663	ORPHA:93314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003521	ORPHA:93314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001156	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001248	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001288	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001498	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001831	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002515	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002650	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002812	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002867	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002869	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002970	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003016	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003088	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003170	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003177	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003336	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003510	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0005819	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0009882	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0010743	ORPHA:93314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000768	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0000914	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0001288	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002808	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002938	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002942	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0002986	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003059	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003121	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003180	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003185	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003311	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003417	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0003907	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0004558	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0008422	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0010228	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0030289	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0030320	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93314	Spondylometaphyseal dysplasia, Kozlowski type		HP:0100864	ORPHA:93314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0001385	ORPHA:93311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0008828	ORPHA:93311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0001288	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0001384	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0002857	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0002970	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0003088	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0003502	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0003839	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0010631	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0030839	ORPHA:93311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0001387	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0001288	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0003170	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0003184	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0003365	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0004268	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0005743	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0005877	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0008419	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0008800	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0030840	ORPHA:93311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93311	Multiple epiphyseal dysplasia type 5		HP:0003418	ORPHA:93311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001072	ORPHA:90289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002829	ORPHA:90289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0011355	ORPHA:90289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0030053	ORPHA:90289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0031359	ORPHA:90289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000164	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000177	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000324	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000504	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000554	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000689	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000953	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001053	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001369	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001371	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002020	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002076	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002232	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002315	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002960	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0003198	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0004426	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0006336	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0009019	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0010783	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0011331	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0011821	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0025474	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0033127	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0100537	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0100560	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0100876	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0100899	ORPHA:90289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000077	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000366	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000490	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000520	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000707	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0000872	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001045	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001250	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001297	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0001626	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002086	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002384	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0002633	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0003202	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0003330	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0008066	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0011138	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0011675	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0030878	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0030880	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0100633	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:90289	Localized scleroderma		HP:0200041	ORPHA:90289	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000713	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000718	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000722	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000729	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000750	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000752	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0001249	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0001328	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0001511	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0001609	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0002312	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0004322	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0009904	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0012471	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0100023	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0100710	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000256	ORPHA:100973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0004209	ORPHA:100973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0012172	ORPHA:100973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000286	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100973	FRAXE intellectual disability		HP:0000426	ORPHA:100973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67041	Hyaluronidase deficiency		HP:0003170	ORPHA:67041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67041	Hyaluronidase deficiency		HP:0004322	ORPHA:67041	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0000962	ORPHA:90280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0000965	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0000988	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0002923	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0010702	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0011123	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0025131	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0025300	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0030350	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0030880	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0030899	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0200042	ORPHA:90280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0002099	ORPHA:90280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0002725	ORPHA:90280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0003493	ORPHA:90280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0003613	ORPHA:90280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0007417	ORPHA:90280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90280	Chilblain lupus		HP:0012325	ORPHA:90280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0001010	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0001075	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0004552	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0007502	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0025474	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0030350	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0100585	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:4000107	ORPHA:90281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0002829	ORPHA:90281	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:90281	Discoid lupus erythematosus		HP:0006739	ORPHA:90281	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0000481	ORPHA:67043	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0000613	ORPHA:67043	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0007856	ORPHA:67043	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0011495	ORPHA:67043	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0200026	ORPHA:67043	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0000518	ORPHA:67043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0001089	ORPHA:67043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0004329	ORPHA:67043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0012122	ORPHA:67043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0012155	ORPHA:67043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0100532	ORPHA:67043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0100583	ORPHA:67043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0000593	ORPHA:67043	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0012040	ORPHA:67043	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67043	Amoebic keratitis		HP:0012804	ORPHA:67043	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0030534	ORPHA:67042	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0000533	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0000572	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0000608	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0000662	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0001141	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0007791	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0011506	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0011510	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0031530	ORPHA:67042	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0000552	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0000613	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0000642	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0001089	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0001099	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0004328	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0007401	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0012628	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0012805	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0500087	ORPHA:67042	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0007906	ORPHA:67042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67042	Late-onset retinal degeneration		HP:0100014	ORPHA:67042	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000248	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000260	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000286	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000316	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000343	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000463	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000470	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000518	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000637	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000774	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000926	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0001238	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0001263	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0002673	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0002693	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0002714	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0002942	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0003071	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0003180	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0003196	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0003300	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0003366	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0005280	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0006454	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0008783	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0011001	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0011326	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0011849	ORPHA:163649	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000347	ORPHA:163649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0002007	ORPHA:163649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0007894	ORPHA:163649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0011329	ORPHA:163649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0100558	ORPHA:163649	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000175	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000218	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000541	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000545	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0000568	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0002879	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0009811	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163649	Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome		HP:0010471	ORPHA:163649	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0100767	ORPHA:439167	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0001511	ORPHA:439167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0001518	ORPHA:439167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0003508	ORPHA:439167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0006266	ORPHA:439167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0011403	ORPHA:439167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0012418	ORPHA:439167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0000717	ORPHA:439167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0000729	ORPHA:439167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0002725	ORPHA:439167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0003613	ORPHA:439167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0012759	ORPHA:439167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0000855	ORPHA:439167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0001627	ORPHA:439167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0002088	ORPHA:439167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0005268	ORPHA:439167	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0008071	ORPHA:439167	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0100021	ORPHA:439167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0100601	ORPHA:439167	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:439167	Placental insufficiency		HP:0100602	ORPHA:439167	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0000455	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0000670	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0000750	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0000966	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0000972	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0001249	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0001954	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0002205	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0005338	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0006297	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0012434	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0012471	ORPHA:363523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0005484	ORPHA:363523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0012115	ORPHA:363523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome		HP:0040196	ORPHA:363523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363523	Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome	NOT	HP:0003160	ORPHA:363523	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0000824	ORPHA:67045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0001249	ORPHA:67045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0004322	ORPHA:67045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0030353	ORPHA:67045	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0000570	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0000657	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0002079	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0002750	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0007979	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0010627	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0011342	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0011755	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0012447	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67045	X-linked intellectual disability with isolated growth hormone deficiency		HP:0040010	ORPHA:67045	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0000028	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0001931	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0004447	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0010972	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0011273	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0012143	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0012145	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0040185	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67044	Thrombocytopenia with congenital dyserythropoietic anemia		HP:0045040	ORPHA:67044	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0000505	ORPHA:67047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0000639	ORPHA:67047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0001249	ORPHA:67047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0001251	ORPHA:67047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0001260	ORPHA:67047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0001266	ORPHA:67047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0001288	ORPHA:67047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0002313	ORPHA:67047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67047	3-methylglutaconic aciduria type 3		HP:0003535	ORPHA:67047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0005318	ORPHA:140989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0001269	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0001297	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002017	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002315	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002326	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002381	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0003470	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0007052	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0007236	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0012229	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0025456	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0100543	ORPHA:140989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0000622	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0000651	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0001250	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0001251	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0001260	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0001945	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002170	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002273	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002385	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0007663	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0010534	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0030588	ORPHA:140989	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0000538	ORPHA:140989	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0001300	ORPHA:140989	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0002321	ORPHA:140989	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0025142	ORPHA:140989	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:140989	Primary angiitis of the central nervous system		HP:0100576	ORPHA:140989	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100974	FRAXF syndrome		HP:0003564	ORPHA:100974	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100974	FRAXF syndrome		HP:0012758	ORPHA:100974	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100974	FRAXF syndrome		HP:0000118	ORPHA:100974	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0000252	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0000750	ORPHA:67046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0001250	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0001259	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0001263	ORPHA:67046	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0001285	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0001332	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0001508	ORPHA:67046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0001943	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0002073	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0002134	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0002240	ORPHA:67046	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67046	3-methylglutaconic aciduria type 1		HP:0003535	ORPHA:67046	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000486	ORPHA:363528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001249	ORPHA:363528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001508	ORPHA:363528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000252	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000286	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000582	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000750	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001257	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001263	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0004322	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0005280	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0008947	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0011220	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0012443	ORPHA:363528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000028	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000047	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000054	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000154	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000218	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000276	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000316	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000324	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000340	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000347	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000348	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000365	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000369	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000400	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000403	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000418	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000448	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000470	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000506	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000664	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000718	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000752	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000824	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000966	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001250	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001357	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001376	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001511	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001561	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001631	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001643	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001762	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001771	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001838	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0002020	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0002553	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0003196	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0007162	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0012408	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0012444	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0012448	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0012471	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0030353	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0031123	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0100710	ORPHA:363528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000164	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000776	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0000821	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001274	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0001288	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0002079	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0002172	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0005879	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0009473	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0009830	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0011968	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0012450	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363528	Intellectual disability-strabismus syndrome		HP:0100702	ORPHA:363528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0001072	ORPHA:100976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0008064	ORPHA:100976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0025092	ORPHA:100976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0040189	ORPHA:100976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0000656	ORPHA:100976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0001019	ORPHA:100976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0001036	ORPHA:100976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0007460	ORPHA:100976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0007479	ORPHA:100976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0010829	ORPHA:100976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0012472	ORPHA:100976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0000966	ORPHA:100976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0000972	ORPHA:100976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0001596	ORPHA:100976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0002828	ORPHA:100976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0008070	ORPHA:100976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis		HP:0008404	ORPHA:100976	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100976	Bathing suit ichthyosis	NOT	HP:0025524	ORPHA:100976	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0000252	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0000365	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0000518	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001249	ORPHA:67048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001250	ORPHA:67048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001252	ORPHA:67048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001257	ORPHA:67048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001263	ORPHA:67048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001410	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001508	ORPHA:67048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001638	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001873	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0001943	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0002195	ORPHA:67048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0003128	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0003535	ORPHA:67048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:67048	3-methylglutaconic aciduria type 4		HP:0007730	ORPHA:67048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000028	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000154	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000174	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000179	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000215	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000306	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000343	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000431	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000463	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000470	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000475	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000574	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000581	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000582	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0000767	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0001156	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0001608	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0001832	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0002162	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0002164	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0002212	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0002750	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0002967	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0003026	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0004322	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0004634	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0005069	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0005280	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0005622	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0006394	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0007665	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0008496	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0008551	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0008839	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0009103	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0009937	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0010306	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0011829	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163654	Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome		HP:0100625	ORPHA:163654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247798	MUTYH-related polyposis		HP:0200063	ORPHA:247798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247798	MUTYH-related polyposis		HP:0005227	ORPHA:247798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247798	MUTYH-related polyposis		HP:0030255	ORPHA:247798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247798	MUTYH-related polyposis		HP:0040276	ORPHA:247798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247798	MUTYH-related polyposis		HP:0100896	ORPHA:247798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247798	MUTYH-related polyposis		HP:0007649	ORPHA:247798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247798	MUTYH-related polyposis	NOT	HP:0100245	ORPHA:247798	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0001057	ORPHA:1114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0001362	ORPHA:1114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0004471	ORPHA:1114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0007383	ORPHA:1114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0010301	ORPHA:1114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0200042	ORPHA:1114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0001770	ORPHA:1114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0003010	ORPHA:1114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0004348	ORPHA:1114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0006101	ORPHA:1114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0010628	ORPHA:1114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:0010783	ORPHA:1114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1114	Aplasia cutis congenita		HP:5200061	ORPHA:1114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0003016	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0003031	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0004002	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0004037	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0005922	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0006429	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0008434	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002827	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0008829	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0008905	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0009381	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0009471	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0009487	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0009778	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0010049	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0010743	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0025264	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0031006	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0031878	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0032649	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0040072	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0100864	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002652	ORPHA:93307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002654	ORPHA:93307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002829	ORPHA:93307	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0000347	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001156	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001371	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001376	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001387	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001762	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001776	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002515	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002812	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002857	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002987	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0003071	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0003088	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0003365	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0003498	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0005616	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0008807	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0008848	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0009824	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0030289	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0031174	ORPHA:93307	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0000175	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0000218	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0000363	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0000369	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0000377	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001385	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001440	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001769	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0001831	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002650	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002947	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93307	Multiple epiphyseal dysplasia type 4		HP:0002986	ORPHA:93307	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2444	Congenital pulmonary airway malformation		HP:0001561	ORPHA:2444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2444	Congenital pulmonary airway malformation		HP:0001622	ORPHA:2444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2444	Congenital pulmonary airway malformation		HP:0002086	ORPHA:2444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2444	Congenital pulmonary airway malformation		HP:0002093	ORPHA:2444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2444	Congenital pulmonary airway malformation		HP:0002103	ORPHA:2444	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0000252	ORPHA:1113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0001804	ORPHA:1113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0004322	ORPHA:1113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0009882	ORPHA:1113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0010185	ORPHA:1113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0001770	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0001798	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0001800	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0001802	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0001830	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0001839	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0005916	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0009773	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1113	Aphalangy-syndactyly-microcephaly syndrome		HP:0100490	ORPHA:1113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93304	Autosomal dominant brachyolmia		HP:0000926	ORPHA:93304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93304	Autosomal dominant brachyolmia		HP:0000944	ORPHA:93304	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93304	Autosomal dominant brachyolmia		HP:0002751	ORPHA:93304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93304	Autosomal dominant brachyolmia		HP:0004322	ORPHA:93304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93304	Autosomal dominant brachyolmia		HP:0004570	ORPHA:93304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93304	Autosomal dominant brachyolmia		HP:0010306	ORPHA:93304	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001315	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002460	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003390	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0007210	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0007327	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0008944	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0009053	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0100290	ORPHA:466768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001249	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001288	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001328	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001337	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001288	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002493	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002495	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003130	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003474	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003484	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003487	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003693	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0004302	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0007002	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0007230	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0008948	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0009046	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0009129	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0009473	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0010830	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0012378	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0012785	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0040131	ORPHA:466768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0000365	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0000467	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001047	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001263	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001276	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001620	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001761	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002167	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002380	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002411	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002500	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002540	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003324	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003325	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003394	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003701	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0003797	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0005879	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0006827	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0006970	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0007269	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0007641	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0007703	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0008959	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0008994	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0008997	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0009027	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0012444	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0012447	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0012473	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0030051	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0030237	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0031947	ORPHA:466768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0000020	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0000252	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0000518	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001250	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001272	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001290	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0001999	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0002747	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466768	Autosomal dominant Charcot-Marie-Tooth disease type 2Z		HP:0006597	ORPHA:466768	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0001839	ORPHA:1112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0002937	ORPHA:1112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0009767	ORPHA:1112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0010173	ORPHA:1112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0000055	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0001555	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0001562	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0001643	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0001770	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0001798	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0002089	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0002644	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0003042	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0004320	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0005916	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0006101	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0008678	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1112	Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome		HP:0012621	ORPHA:1112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000160	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000252	ORPHA:1110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000303	ORPHA:1110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000324	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000325	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000337	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000358	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000400	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000426	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000444	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000494	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000670	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0000708	ORPHA:1110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0001249	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0001252	ORPHA:1110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0001511	ORPHA:1110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0002623	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0002714	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0002970	ORPHA:1110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0003272	ORPHA:1110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0010669	ORPHA:1110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0012303	ORPHA:1110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1110	Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome		HP:0100026	ORPHA:1110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0012165	ORPHA:2440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0001839	ORPHA:2440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0004058	ORPHA:2440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0006101	ORPHA:2440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0000407	ORPHA:2440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0000526	ORPHA:2440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0001171	ORPHA:2440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2440	Isolated split hand-split foot malformation		HP:0004050	ORPHA:2440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0001288	ORPHA:93308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0001385	ORPHA:93308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0003026	ORPHA:93308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0003365	ORPHA:93308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0030839	ORPHA:93308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0030973	ORPHA:93308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0001376	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0001387	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0002515	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0002663	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0002758	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0003170	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0003498	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0006094	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0030840	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0045086	ORPHA:93308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0002812	ORPHA:93308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0002857	ORPHA:93308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0002970	ORPHA:93308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1		HP:0005743	ORPHA:93308	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93308	Multiple epiphyseal dysplasia type 1	NOT	HP:0001156	ORPHA:93308	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0000767	ORPHA:93302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0000926	ORPHA:93302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0002650	ORPHA:93302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0003312	ORPHA:93302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0004322	ORPHA:93302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0006610	ORPHA:93302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0010306	ORPHA:93302	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93302	Brachyolmia, Maroteaux type		HP:0010653	ORPHA:93302	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1118	Fibular aplasia-ectrodactyly syndrome		HP:0001622	ORPHA:1118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1118	Fibular aplasia-ectrodactyly syndrome		HP:0001171	ORPHA:1118	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1118	Fibular aplasia-ectrodactyly syndrome		HP:0006492	ORPHA:1118	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1118	Fibular aplasia-ectrodactyly syndrome		HP:0040071	ORPHA:1118	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0000924	ORPHA:1117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0001057	ORPHA:1117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0001287	ORPHA:1117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0001362	ORPHA:1117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0001892	ORPHA:1117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0001928	ORPHA:1117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0006934	ORPHA:1117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0007703	ORPHA:1117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0011003	ORPHA:1117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0012639	ORPHA:1117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1117	Aplasia cutis-myopia syndrome		HP:0200042	ORPHA:1117	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0000545	ORPHA:1116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0000567	ORPHA:1116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0001004	ORPHA:1116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0001362	ORPHA:1116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0001888	ORPHA:1116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0001892	ORPHA:1116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0001928	ORPHA:1116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0002024	ORPHA:1116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0003075	ORPHA:1116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0004209	ORPHA:1116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0004313	ORPHA:1116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0007598	ORPHA:1116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1116	Aplasia cutis congenita-intestinal lymphangiectasia syndrome		HP:0011362	ORPHA:1116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000085	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000126	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000218	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000278	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000280	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000308	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000316	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000347	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000356	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000358	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000358	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000369	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000494	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000506	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001166	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001270	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001319	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001363	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001382	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001511	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001519	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001548	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001999	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0002705	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0007642	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0008714	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0009471	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0009540	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0012210	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0012758	ORPHA:314585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000193	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000238	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000256	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000262	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000268	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000272	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000303	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000319	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000410	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000431	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000486	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000676	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000678	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0000766	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001176	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001250	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001274	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001305	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001347	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001623	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001653	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0001845	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0002092	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0002315	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0002650	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0002667	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0003396	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0004209	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0005180	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0006143	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0006610	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0008519	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0010653	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0012444	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314585	15q overgrowth syndrome		HP:0030680	ORPHA:314585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0000618	ORPHA:77299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0007633	ORPHA:77299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0000252	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0001257	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0002013	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0002376	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0002506	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0006956	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0007162	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0007366	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0007371	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0030215	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0031165	ORPHA:77299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0002123	ORPHA:77299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0002197	ORPHA:77299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0006855	ORPHA:77299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0007361	ORPHA:77299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0011174	ORPHA:77299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0031358	ORPHA:77299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77299	Microphthalmia-brain atrophy syndrome		HP:0100703	ORPHA:77299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000028	ORPHA:77298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000047	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000238	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000365	ORPHA:77298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000528	ORPHA:77298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000568	ORPHA:77298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000572	ORPHA:77298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000612	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000647	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0000878	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0001249	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0001263	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0001274	ORPHA:77298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0001360	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0001510	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0001629	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0001643	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0002032	ORPHA:77298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0002575	ORPHA:77298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0002937	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0003468	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77298	Anophthalmia/microphthalmia-esophageal atresia syndrome		HP:0008736	ORPHA:77298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0001824	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0001945	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002653	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002754	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002829	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0003025	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0004326	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0004810	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0004840	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0005561	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0012647	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0200034	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0200039	ORPHA:77297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0000969	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0001061	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0001508	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0001744	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0001974	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002240	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002315	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0003326	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0011001	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0100769	ORPHA:77297	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0000093	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0001371	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002024	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002113	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002659	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0002907	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0011123	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0012735	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77297	Majeed syndrome		HP:0100820	ORPHA:77297	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0004438	ORPHA:77296	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000707	ORPHA:77296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000708	ORPHA:77296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000818	ORPHA:77296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0001513	ORPHA:77296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002315	ORPHA:77296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0032245	ORPHA:77296	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000819	ORPHA:77296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0001007	ORPHA:77296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002076	ORPHA:77296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002120	ORPHA:77296	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000716	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000725	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000820	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000821	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000822	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0000939	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0001061	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0001250	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0001348	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002149	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002310	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002321	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002345	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002354	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0002758	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0003124	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0012444	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0031589	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77296	Morgagni-Stewart-Morel syndrome		HP:0100543	ORPHA:77296	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0000823	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0000938	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0000939	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001410	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001744	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001873	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001971	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002155	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002240	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002750	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0003077	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0003119	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0003141	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0003233	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0004322	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0006515	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0006520	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0006530	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0010729	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0012415	ORPHA:77293	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0000707	ORPHA:77293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002194	ORPHA:77293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0004887	ORPHA:77293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0009830	ORPHA:77293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0030353	ORPHA:77293	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0000639	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0000708	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0000716	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001081	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001249	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001251	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001317	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001328	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001394	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001399	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001654	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001677	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001892	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0001973	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002121	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002186	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002725	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002756	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0002896	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0004836	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0007018	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:77293	Chronic visceral acid sphingomyelinase deficiency		HP:0007302	ORPHA:77293	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002133	ORPHA:363558	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0025373	ORPHA:363558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0032867	ORPHA:363558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0032894	ORPHA:363558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0001945	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002384	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002457	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002922	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002960	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0004302	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0007183	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0007334	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0010845	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0011154	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0011468	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0012229	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0020217	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0011117	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0033716	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0033717	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0100543	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0410263	ORPHA:363558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0000708	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0001289	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002283	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002315	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0002383	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0010841	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0010850	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0011198	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0012378	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0012696	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0030915	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0031358	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0032794	ORPHA:363558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0012751	ORPHA:363558	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363558	New-onset refractory status epilepticus		HP:0031475	ORPHA:363558	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529970	Male infertility due to acephalic spermatozoa		HP:0003251	ORPHA:529970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529970	Male infertility due to acephalic spermatozoa		HP:0012869	ORPHA:529970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529970	Male infertility due to acephalic spermatozoa		HP:0000798	ORPHA:529970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529970	Male infertility due to acephalic spermatozoa		HP:0012207	ORPHA:529970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529970	Male infertility due to acephalic spermatozoa		HP:0012867	ORPHA:529970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529970	Male infertility due to acephalic spermatozoa	NOT	HP:0002916	ORPHA:529970	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:529970	Male infertility due to acephalic spermatozoa	NOT	HP:0008226	ORPHA:529970	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000175	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000316	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000358	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000453	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000528	ORPHA:1104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000581	ORPHA:1104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000612	ORPHA:1104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0000625	ORPHA:1104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0002006	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0002414	ORPHA:1104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0100337	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0003422	ORPHA:1104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0004097	ORPHA:1104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0005105	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0009906	ORPHA:1104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1104	Anophthalmia plus syndrome		HP:0100335	ORPHA:1104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0000252	ORPHA:2435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0000772	ORPHA:2435	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0000995	ORPHA:2435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0001053	ORPHA:2435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0001249	ORPHA:2435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0004322	ORPHA:2435	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0007400	ORPHA:2435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2435	Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome		HP:0012733	ORPHA:2435	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0000235	ORPHA:2432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0000337	ORPHA:2432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0000482	ORPHA:2432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0000568	ORPHA:2432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0001520	ORPHA:2432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0002205	ORPHA:2432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0002240	ORPHA:2432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0002093	ORPHA:2432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0002683	ORPHA:2432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0007957	ORPHA:2432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2432	Macrosomia-microphthalmia-cleft palate syndrome		HP:0009099	ORPHA:2432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000023	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000028	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000268	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000303	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000327	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000343	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000485	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000526	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000528	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000545	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000587	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000598	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0000767	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0001131	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0001357	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0001537	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0001653	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0001704	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0001762	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0002650	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0002705	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0004327	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0005180	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0009004	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0009465	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0030680	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0100490	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1101	Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome		HP:0200007	ORPHA:1101	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2430	Congenital macroglossia		HP:0000158	ORPHA:2430	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2430	Congenital macroglossia		HP:0000821	ORPHA:2430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2430	Congenital macroglossia		HP:0001067	ORPHA:2430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2430	Congenital macroglossia		HP:0500030	ORPHA:2430	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0001300	ORPHA:411602	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0000651	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002015	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002304	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002322	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002359	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002548	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0004409	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0005340	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0012450	ORPHA:411602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0000338	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0000713	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0000716	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0000741	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0000744	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0001268	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0001332	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0001824	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002063	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002067	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002120	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002171	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002172	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002360	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002362	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0002367	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0003394	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0004926	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0031435	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0100315	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0100660	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0100710	ORPHA:411602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0000726	ORPHA:411602	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411602	Hereditary late-onset Parkinson disease		HP:0100753	ORPHA:411602	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0100665	ORPHA:528647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0000282	ORPHA:528647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0005225	ORPHA:528647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0010742	ORPHA:528647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0012027	ORPHA:528647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0001892	ORPHA:528647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0002027	ORPHA:528647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0002099	ORPHA:528647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0031188	ORPHA:528647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0040315	ORPHA:528647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh		HP:0012378	ORPHA:528647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh	NOT	HP:0001025	ORPHA:528647	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:528647	Hereditary angioedema with normal C1Inh	NOT	HP:0045042	ORPHA:528647	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0100832	ORPHA:420556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0000360	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0000613	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0000662	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0000716	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0000737	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0000739	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0001337	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0002076	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0002321	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0002360	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0003401	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0007302	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0012378	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0030786	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0030833	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0031987	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:5200217	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:5200218	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:6001103	ORPHA:420556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0002172	ORPHA:420556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0012173	ORPHA:420556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome		HP:0033630	ORPHA:420556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420556	Visual snow syndrome	NOT	HP:0002077	ORPHA:420556	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000175	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000272	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000347	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000377	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000400	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0001770	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0001839	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0005321	ORPHA:2439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000218	ORPHA:2439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000407	ORPHA:2439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0000678	ORPHA:2439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2439	Patterson-Stevenson-Fontaine syndrome		HP:0004467	ORPHA:2439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000010	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000047	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000074	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000076	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000130	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000486	ORPHA:2438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000795	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000813	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0000960	ORPHA:2438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0001162	ORPHA:2438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0001629	ORPHA:2438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0004209	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0005048	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0005268	ORPHA:2438	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0006110	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0007477	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0008080	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0008551	ORPHA:2438	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0009623	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0009778	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0009882	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0010034	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0010105	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0010109	ORPHA:2438	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2438	Hand-foot-genital syndrome		HP:0011937	ORPHA:2438	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000327	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000534	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000568	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000581	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001770	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001852	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0002007	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0002814	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0002817	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0005048	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0005916	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0006101	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0011220	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0011478	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0100240	ORPHA:1106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000204	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000358	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000648	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001162	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001172	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0009380	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001215	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001508	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001849	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0002342	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0002982	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0003026	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0003038	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0003312	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0004209	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0004322	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0005280	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0005736	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0007598	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0008368	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0009748	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0010864	ORPHA:1106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000028	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000085	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000175	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000218	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000233	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000238	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000343	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0000347	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001522	ORPHA:1106	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001572	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001762	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001830	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0002139	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0002827	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0003042	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0005293	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0001382	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0006487	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0010650	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1106	Microphthalmia with limb anomalies		HP:0011304	ORPHA:1106	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000079	ORPHA:2437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000126	ORPHA:2437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0001839	ORPHA:2437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0002414	ORPHA:2437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0012300	ORPHA:2437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0025193	ORPHA:2437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0100257	ORPHA:2437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000218	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000238	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000340	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000347	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000358	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000474	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000582	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0000954	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0001233	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0001234	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0001651	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0002089	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0002475	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0002557	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0002575	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0002944	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0003298	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0006097	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0006610	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0008589	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0008593	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0008676	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0009112	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0010539	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0010704	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0045026	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2437	Czeizel-Losonci syndrome		HP:0100760	ORPHA:2437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000218	ORPHA:314588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001263	ORPHA:314588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001507	ORPHA:314588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001999	ORPHA:314588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000077	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000126	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000278	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000316	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000347	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000369	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000506	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000929	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001252	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001328	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001363	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001520	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0003517	ORPHA:314588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000034	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000085	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000113	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000238	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000378	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000407	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000486	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000766	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0000811	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001131	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001166	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001305	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001371	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001511	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001627	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001631	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0001643	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0002089	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0002650	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0002667	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0002808	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0003396	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0008551	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0010946	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0011039	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0012304	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0012385	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314588	Distal triplication 15q syndrome		HP:0100790	ORPHA:314588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0001263	ORPHA:529965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0001290	ORPHA:529965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0000307	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0000494	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0000574	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0001249	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0002007	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0007874	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0010648	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0011098	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0011800	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0012393	ORPHA:529965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0000256	ORPHA:529965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0000729	ORPHA:529965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0000733	ORPHA:529965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0001211	ORPHA:529965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0001250	ORPHA:529965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0002721	ORPHA:529965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529965	Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome		HP:0008897	ORPHA:529965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000750	ORPHA:529962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0001256	ORPHA:529962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0001956	ORPHA:529962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000219	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000316	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000322	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000325	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000347	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000403	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000431	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000470	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000475	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000490	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000494	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000508	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000545	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000574	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000664	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000692	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000708	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000739	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0001250	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0001531	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0002650	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0002967	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0003019	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0003028	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0008551	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0008607	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0008935	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0009824	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0010794	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0011800	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0011968	ORPHA:529962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000362	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000712	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000718	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000738	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000869	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0001657	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0011304	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0011648	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0200053	ORPHA:529962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0000076	ORPHA:529962	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0001642	ORPHA:529962	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome		HP:0012683	ORPHA:529962	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529962	17q24.2 microdeletion syndrome	NOT	HP:0000824	ORPHA:529962	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0002069	ORPHA:363549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0007103	ORPHA:363549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0007185	ORPHA:363549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0011172	ORPHA:363549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0012705	ORPHA:363549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0031691	ORPHA:363549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0032308	ORPHA:363549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0032894	ORPHA:363549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0033349	ORPHA:363549	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0007738	ORPHA:363549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0031475	ORPHA:363549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363549	Acute encephalopathy with biphasic seizures and late reduced diffusion		HP:0011665	ORPHA:363549	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0000853	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0001482	ORPHA:163634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0001510	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0002015	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0002650	ORPHA:163634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0002653	ORPHA:163634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0002757	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0002797	ORPHA:163634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0002893	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0002897	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0003002	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0004322	ORPHA:163634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0004936	ORPHA:163634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0005701	ORPHA:163634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0006765	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0006824	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0007461	ORPHA:163634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0009592	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0100021	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0100242	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0100615	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0100641	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0100733	ORPHA:163634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163634	Maffucci syndrome		HP:0100777	ORPHA:163634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0011123	ORPHA:39812	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0000155	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002014	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002719	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002910	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0010280	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0040186	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0200041	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0200123	ORPHA:39812	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0000737	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0000952	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0001369	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0001433	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0001649	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002013	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002018	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002027	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002090	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002113	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002904	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002996	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0003155	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0003202	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0004386	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0006467	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0012156	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0031123	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0031359	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0031452	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0040189	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0100533	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0100537	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0100614	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0200119	ORPHA:39812	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0000211	ORPHA:39812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0000633	ORPHA:39812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0001508	ORPHA:39812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0002716	ORPHA:39812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0005198	ORPHA:39812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0005679	ORPHA:39812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:39812	Graft versus host disease		HP:0009125	ORPHA:39812	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000154	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000219	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000232	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000256	ORPHA:2429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000280	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000303	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000322	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000336	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000337	ORPHA:2429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000348	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000490	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000574	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0000664	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0001249	ORPHA:2429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0001250	ORPHA:2429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0001257	ORPHA:2429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0001288	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0001347	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0001956	ORPHA:2429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0002162	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0002650	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0002808	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0003196	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2429	Macrocephaly-spastic paraplegia-dysmorphism syndrome		HP:0100874	ORPHA:2429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0000218	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0000219	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0000248	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0000369	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0000400	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0000494	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0000767	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0001363	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0002007	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0002021	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0004322	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0005280	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0008689	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314575	Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome		HP:0008947	ORPHA:314575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0001382	ORPHA:93360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002652	ORPHA:93360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002656	ORPHA:93360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0004322	ORPHA:93360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0011800	ORPHA:93360	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0000926	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0001238	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0001518	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0001602	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0001832	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002651	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002663	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002761	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002857	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002970	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0003025	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0003088	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0006014	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0006236	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0008755	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0008857	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0009815	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0010674	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0012095	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0012368	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0031367	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0040064	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0100168	ORPHA:93360	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0000486	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0001250	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002650	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002751	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002808	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002827	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0002987	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0003048	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0003370	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0004875	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0005619	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0006536	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93360	Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type		HP:0030043	ORPHA:93360	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0000762	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0001265	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0001609	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0003198	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0003458	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0003557	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0007340	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0008180	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0008619	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0009063	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0009830	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0010219	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0012548	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0030774	ORPHA:397744	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0001284	ORPHA:397744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0001337	ORPHA:397744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0003701	ORPHA:397744	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0001250	ORPHA:397744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome		HP:0001369	ORPHA:397744	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome	NOT	HP:0001605	ORPHA:397744	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:397744	Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome	NOT	HP:0002015	ORPHA:397744	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0000282	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0000988	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0001386	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0002014	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0002017	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0002027	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0011855	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0012027	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0012531	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0025527	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0031188	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0034204	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0045042	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0100665	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0100748	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:6000507	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:6001012	ORPHA:528623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0002315	ORPHA:528623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0003401	ORPHA:528623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0012378	ORPHA:528623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0025406	ORPHA:528623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency		HP:0012271	ORPHA:528623	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency	NOT	HP:0000989	ORPHA:528623	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:528623	Hereditary angioedema with C1Inh deficiency	NOT	HP:0001025	ORPHA:528623	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000119	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000126	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000276	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000280	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000431	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000637	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000750	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001249	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001252	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001270	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001627	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002465	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0011039	ORPHA:453499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000028	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000076	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000175	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000194	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000218	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000221	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000252	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000365	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000430	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000508	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000586	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001315	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001363	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001385	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001508	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001511	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001629	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001883	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002019	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002020	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002079	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002579	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002650	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002714	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0003186	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0003422	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0005487	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0010880	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0012332	ORPHA:453499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000158	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000193	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000476	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000589	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000666	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000677	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000821	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0000938	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001250	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001284	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001324	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001357	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001631	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001647	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0001954	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002046	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002202	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0002282	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0003396	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0003763	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0004467	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0004970	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0006695	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0007328	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0007550	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0009794	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0011470	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0025487	ORPHA:453499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:453499	Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome		HP:0011024	ORPHA:453499	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000023	ORPHA:2412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000079	ORPHA:2412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000160	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000174	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000272	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000286	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000316	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000364	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000431	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000457	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0000463	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0001374	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0001643	ORPHA:2412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0001671	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0001702	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0002815	ORPHA:2412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0004097	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0001382	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0010759	ORPHA:2412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2412	Dislocation of the hip-dysmorphism syndrome		HP:0011328	ORPHA:2412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000013	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000104	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000137	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000142	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000175	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000322	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000411	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000470	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000574	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000664	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000786	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0000914	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0001007	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0001061	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0001156	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0001513	ORPHA:247768	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0002292	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0002967	ORPHA:247768	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0004322	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0009890	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0009937	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247768	Müllerian aplasia and hyperandrogenism		HP:0030088	ORPHA:247768	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0000518	ORPHA:2410	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0000815	ORPHA:2410	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0000144	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0000786	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0000823	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0000837	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0000939	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0002750	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0008187	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0008240	ORPHA:2410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0002757	ORPHA:2410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0004322	ORPHA:2410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2410	Hypergonadotropic hypogonadism-cataract syndrome		HP:0004349	ORPHA:2410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000768	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000772	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000926	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000939	ORPHA:93351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0000944	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001169	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001191	ORPHA:93351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001288	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001367	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001376	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001763	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0001769	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002651	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002758	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002812	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002829	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002857	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0002983	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0004279	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0005048	ORPHA:93351	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0005930	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0008839	ORPHA:93351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0008873	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0009824	ORPHA:93351	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0010049	ORPHA:93351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93351	Spondyloepimetaphyseal dysplasia, Irapa type		HP:0010743	ORPHA:93351	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0000926	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002650	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002829	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003015	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003016	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003026	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003088	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003468	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003498	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003510	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0005257	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0005930	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0006462	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0008463	ORPHA:93352	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0000470	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001382	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001433	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001602	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0001609	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002663	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002777	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002781	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002953	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002970	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0002979	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003025	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003099	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003270	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0003307	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0008418	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0008450	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0009826	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93352	Spondyloepimetaphyseal dysplasia, Shohat type		HP:0025426	ORPHA:93352	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000010	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000122	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000306	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000316	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000348	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000411	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000431	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000455	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000463	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000490	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000609	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000924	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000938	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000953	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0000998	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001249	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001251	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001263	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001319	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001369	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001537	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001761	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0001999	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002020	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002058	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002080	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002100	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002119	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002123	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002162	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002403	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002643	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002718	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002841	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002850	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0003307	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0003460	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0003765	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0004313	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0004429	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0005280	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0005387	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0032218	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0006610	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0007678	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0009098	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0009650	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0009844	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0009891	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0010282	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0010579	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0010750	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0010976	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0025540	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0031632	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0031381	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0031382	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0032132	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0032140	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0040022	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0040024	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0040025	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0040218	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0040288	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0100540	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0410018	ORPHA:221139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002007	ORPHA:221139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0002014	ORPHA:221139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221139	Combined immunodeficiency with facio-oculo-skeletal anomalies		HP:0004425	ORPHA:221139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000925	ORPHA:93357	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000926	ORPHA:93357	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001999	ORPHA:93357	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0005280	ORPHA:93357	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0008873	ORPHA:93357	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0011800	ORPHA:93357	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001156	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001511	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001518	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002857	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003025	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0004586	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0008905	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0009826	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0031367	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0100864	ORPHA:93357	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000047	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000276	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000286	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000303	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000445	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000463	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000518	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000639	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000691	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000696	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000821	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0000826	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001169	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001263	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001377	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001382	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001607	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001621	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001763	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001769	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001773	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0001875	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002007	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002308	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002650	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002663	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002751	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002761	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002812	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002827	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0002938	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003015	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003016	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003026	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003027	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003182	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003196	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003370	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0003895	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0004279	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0004313	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0004482	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0004603	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0004646	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0004944	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0005446	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0005743	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0006336	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0006532	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0006889	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0007707	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0010234	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0010585	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0010740	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0010941	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0011220	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0025492	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0030043	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0030833	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0030834	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0030839	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0040221	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93357	SPONASTRIME dysplasia		HP:0100559	ORPHA:93357	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0000124	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0000531	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0000613	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0001508	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0001510	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0001941	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0001944	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0001959	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0001969	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0001994	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0002013	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0002019	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0002148	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0002748	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0002900	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0003076	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0003109	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0003111	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0003126	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0003355	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0004918	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0100511	ORPHA:411629	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0000481	ORPHA:411629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0000580	ORPHA:411629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0002926	ORPHA:411629	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0002500	ORPHA:411629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411629	Infantile nephropathic cystinosis		HP:0100543	ORPHA:411629	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000750	ORPHA:163681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001250	ORPHA:163681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0002269	ORPHA:163681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0007359	ORPHA:163681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0012757	ORPHA:163681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0031936	ORPHA:163681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001263	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001268	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001270	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0002465	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0007064	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0007334	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0010845	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0010864	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0011182	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0011198	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0012001	ORPHA:163681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000316	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000494	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000639	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000708	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000717	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000718	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000742	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000744	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000752	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000817	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0000826	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001251	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001252	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001265	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001284	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001344	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001513	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0001761	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0002061	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0002240	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0002342	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0004879	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0006855	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0006970	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0010863	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0011193	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0011968	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0012166	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0012171	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0025160	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0100021	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163681	CNTNAP2-related developmental and epileptic encephalopathy		HP:0100258	ORPHA:163681	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0000961	ORPHA:2414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0001510	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0001541	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0001635	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0001642	ORPHA:2414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0001744	ORPHA:2414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0001789	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0002020	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0002092	ORPHA:2414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0002098	ORPHA:2414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0002202	ORPHA:2414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0002240	ORPHA:2414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0005180	ORPHA:2414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0006510	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0011852	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2414	Congenital pulmonary lymphangiectasia		HP:0012735	ORPHA:2414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002970	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002980	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0002982	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003015	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003025	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003071	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0003498	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0004566	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0005086	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0006385	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0010585	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93356	Spondyloepimetaphyseal dysplasia, Missouri type		HP:0025369	ORPHA:93356	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001256	ORPHA:476126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001263	ORPHA:476126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0002465	ORPHA:476126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000164	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000324	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000347	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000348	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000664	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000678	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000708	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000729	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001182	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0002650	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0002719	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0004691	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0008872	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0011451	ORPHA:476126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000020	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000218	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000286	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000343	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000486	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000646	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000706	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000718	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000722	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000733	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000742	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0000767	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001155	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001250	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001328	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001337	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001344	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001508	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001674	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0001763	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0002033	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0002066	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0002360	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0002808	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0003072	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0003196	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0004209	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0004279	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0005484	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0006889	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0007018	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0007970	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0009659	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0010035	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0011471	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0011908	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0012450	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:476126	Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome		HP:0200006	ORPHA:476126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2400	Peripheral motor neuropathy-dysautonomia syndrome		HP:0000975	ORPHA:2400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2400	Peripheral motor neuropathy-dysautonomia syndrome		HP:0001063	ORPHA:2400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2400	Peripheral motor neuropathy-dysautonomia syndrome		HP:0001265	ORPHA:2400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2400	Peripheral motor neuropathy-dysautonomia syndrome		HP:0001387	ORPHA:2400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2400	Peripheral motor neuropathy-dysautonomia syndrome		HP:0002571	ORPHA:2400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2400	Peripheral motor neuropathy-dysautonomia syndrome		HP:0003202	ORPHA:2400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2400	Peripheral motor neuropathy-dysautonomia syndrome		HP:0003457	ORPHA:2400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0000268	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0000278	ORPHA:163690	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0000286	ORPHA:163690	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0000508	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0000787	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0001252	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0001508	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0001510	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0001558	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0001611	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0002007	ORPHA:163690	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0002591	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0003131	ORPHA:163690	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163690	Hypotonia-cystinuria syndrome		HP:0012378	ORPHA:163690	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000175	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000252	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000369	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000444	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000494	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000520	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000680	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000776	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0001087	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0001363	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0001510	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0001511	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0002012	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0007370	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0011344	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0030680	ORPHA:2409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000023	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000047	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000078	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000237	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000238	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000243	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000278	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000327	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000347	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000348	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000453	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000485	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000572	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000577	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000592	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000938	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000939	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0000954	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0001269	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0001680	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0002021	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0002705	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0002714	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0003194	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0003196	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0004439	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0004554	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0005211	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0005442	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0006695	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0007957	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0008689	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0011087	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0025247	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0100538	ORPHA:2409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2409	Lowry-MacLean syndrome		HP:0001250	ORPHA:2409	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0000794	ORPHA:34145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0001919	ORPHA:34145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0002907	ORPHA:34145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0012587	ORPHA:34145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0012595	ORPHA:34145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0000083	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0000099	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0000282	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0000822	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0001394	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0001541	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0002608	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0003261	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0030830	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0031504	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0033316	ORPHA:34145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34145	Immunoglobulin A nephropathy		HP:0012593	ORPHA:34145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2408	Lowe-Kohn-Cohen syndrome		HP:0000112	ORPHA:2408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2408	Lowe-Kohn-Cohen syndrome		HP:0000384	ORPHA:2408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2408	Lowe-Kohn-Cohen syndrome		HP:0000407	ORPHA:2408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2408	Lowe-Kohn-Cohen syndrome		HP:0002023	ORPHA:2408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2408	Lowe-Kohn-Cohen syndrome		HP:0012732	ORPHA:2408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0001607	ORPHA:2407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0200042	ORPHA:2407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0000670	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0000684	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0000691	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0001030	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0001609	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0005348	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0006297	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0008066	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0008404	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0012804	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0100803	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0200020	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0200041	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0200097	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0430007	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:6000956	ORPHA:2407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0000421	ORPHA:2407	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0000505	ORPHA:2407	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0004840	ORPHA:2407	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2407	Laryngo-onycho-cutaneous syndrome		HP:0008777	ORPHA:2407	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0000365	ORPHA:2406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0000478	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0000504	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0000651	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0000708	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0001257	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0001276	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0001608	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0002093	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0002205	ORPHA:2406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0002273	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0002425	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0002445	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0003781	ORPHA:2406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0011968	ORPHA:2406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2406	Locked-in syndrome		HP:0100021	ORPHA:2406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0003015	ORPHA:93346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0045060	ORPHA:93346	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000162	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000280	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000316	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000347	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000365	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000545	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0003026	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0003173	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0003468	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0008462	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0010585	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0012368	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0100569	ORPHA:93346	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000670	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0000926	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0001216	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0002176	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0002795	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0005193	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0008755	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0008800	ORPHA:93346	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93346	Spondyloepimetaphyseal dysplasia congenita, Strudwick type		HP:0009800	ORPHA:93346	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0000135	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0000358	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0000527	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0000787	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001250	ORPHA:163693	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001252	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001263	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001508	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001510	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001558	ORPHA:163693	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001611	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0001943	ORPHA:163693	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0002007	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0002342	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0002901	ORPHA:163693	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0003128	ORPHA:163693	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0003131	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0005280	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163693	2p21 microdeletion syndrome		HP:0200125	ORPHA:163693	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0010803	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0010804	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0012553	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0012555	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000154	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000252	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000280	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000286	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000316	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000343	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000400	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000431	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000445	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000527	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000574	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000684	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0001250	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0001290	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0001344	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0001488	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0001847	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0002019	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0002058	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0002353	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0004322	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0005280	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0010624	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0010864	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0011304	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0011344	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0012443	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0012471	ORPHA:420561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000194	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000212	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000218	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000232	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000272	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000293	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000294	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0000463	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0001802	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0001804	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0006016	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0009648	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0009660	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0009882	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0009890	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420561	Temple-Baraitser syndrome		HP:0009928	ORPHA:420561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231393	Beta-thalassemia-X-linked thrombocytopenia syndrome		HP:0001744	ORPHA:231393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231393	Beta-thalassemia-X-linked thrombocytopenia syndrome		HP:0001873	ORPHA:231393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231393	Beta-thalassemia-X-linked thrombocytopenia syndrome		HP:0001892	ORPHA:231393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231393	Beta-thalassemia-X-linked thrombocytopenia syndrome		HP:0001903	ORPHA:231393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231393	Beta-thalassemia-X-linked thrombocytopenia syndrome		HP:0011869	ORPHA:231393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231393	Beta-thalassemia-X-linked thrombocytopenia syndrome		HP:0011902	ORPHA:231393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0000722	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0001260	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0001300	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0002313	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0002339	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0001288	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0002453	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0002454	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0003477	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0010663	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0010994	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0012048	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397725	COASY protein-associated neurodegeneration		HP:0100543	ORPHA:397725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000252	ORPHA:280763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001252	ORPHA:280763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0007020	ORPHA:280763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0010864	ORPHA:280763	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000280	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000297	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000414	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001257	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001263	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001272	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001332	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001347	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002120	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002307	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001288	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002464	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002465	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002515	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0003487	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0004322	ORPHA:280763	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000154	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000218	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000322	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000341	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000733	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001250	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0001763	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002079	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002518	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0010803	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0025502	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0100962	ORPHA:280763	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000486	ORPHA:280763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0000646	ORPHA:280763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002761	ORPHA:280763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0002816	ORPHA:280763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280763	Severe intellectual disability and progressive spastic paraplegia		HP:0008807	ORPHA:280763	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000750	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001256	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001290	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001533	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001611	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001711	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001763	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001999	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000286	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000316	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000322	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000325	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000494	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000687	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000717	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000718	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000823	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001250	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001251	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001321	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001357	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001382	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001508	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001629	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001631	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001643	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001655	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001667	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001712	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0001822	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002007	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002020	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002079	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002080	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002465	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002558	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002684	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002870	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0004209	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0004684	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0005180	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0007024	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0007083	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0007099	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0007449	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0008689	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0010316	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0010627	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0011098	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0012471	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0030872	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0032009	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0040288	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0004482	ORPHA:466791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000194	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000272	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000276	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000426	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000446	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000448	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000486	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000545	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000582	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000678	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000739	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002033	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002194	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002421	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002705	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0002751	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0006989	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0009703	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0011968	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0100962	ORPHA:466791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000028	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000154	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome		HP:0000219	ORPHA:466791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0040322	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0010472	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0012379	ORPHA:100924	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000707	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0001289	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000713	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000739	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000711	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000738	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0031258	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0007159	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000741	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000716	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0100852	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0009830	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0007178	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000763	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0004302	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0001324	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002027	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002018	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002572	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002019	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0003270	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002014	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency	NOT	HP:0011121	ORPHA:100924	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0001271	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002902	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002086	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0005547	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0012217	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0012187	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0033010	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0030272	ORPHA:100924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0003690	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0001260	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0002093	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0005946	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0001256	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000717	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0000365	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0001288	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:100924	Porphyria due to ALA dehydratase deficiency		HP:0006466	ORPHA:100924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0000926	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0002815	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0002867	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0003028	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0003468	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0003521	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0004322	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0005193	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0010665	ORPHA:163665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0001256	ORPHA:163665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163665	Spondyloepiphyseal dysplasia tarda, Kohn type		HP:0002342	ORPHA:163665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411641	Ocular cystinosis		HP:0000505	ORPHA:411641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411641	Ocular cystinosis		HP:0000531	ORPHA:411641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411641	Ocular cystinosis		HP:0000613	ORPHA:411641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411641	Ocular cystinosis		HP:0032639	ORPHA:411641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0000641	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001152	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001256	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001263	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001265	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001395	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001433	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001945	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0002066	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0002073	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0002080	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0002359	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0003401	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0003474	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0006554	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0006855	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0009053	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0009055	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0009830	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0025268	ORPHA:466794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0000648	ORPHA:466794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001257	ORPHA:466794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001347	ORPHA:466794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome		HP:0001762	ORPHA:466794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466794	Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome	NOT	HP:0007663	ORPHA:466794	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000009	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000012	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000014	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000017	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000058	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000078	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000140	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000795	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0030016	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0034267	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0100515	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0100518	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0100577	ORPHA:37202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000716	ORPHA:37202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0002960	ORPHA:37202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0011118	ORPHA:37202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0011227	ORPHA:37202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0000142	ORPHA:37202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:37202	Interstitial cystitis		HP:0500005	ORPHA:37202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000256	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000470	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000882	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000946	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0001156	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0001374	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0002987	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0003041	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0003097	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0003943	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0004987	ORPHA:93333	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000369	ORPHA:93333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0002693	ORPHA:93333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0004322	ORPHA:93333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000316	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000365	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000377	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000402	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000486	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000490	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0000581	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0002007	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0002162	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93333	Pelviscapular dysplasia		HP:0005989	ORPHA:93333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0000982	ORPHA:498359	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0007407	ORPHA:498359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0007410	ORPHA:498359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0025080	ORPHA:498359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0031248	ORPHA:498359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0031289	ORPHA:498359	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0000969	ORPHA:498359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0001047	ORPHA:498359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0002725	ORPHA:498359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0005425	ORPHA:498359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0006261	ORPHA:498359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:498359	Aquagenic palmoplantar keratoderma		HP:0200035	ORPHA:498359	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0000028	ORPHA:93328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0000048	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0000062	ORPHA:93328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0000272	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0000316	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0000343	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0000347	ORPHA:93328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0002007	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0002999	ORPHA:93328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0003042	ORPHA:93328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0003196	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0004279	ORPHA:93328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0005280	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0005792	ORPHA:93328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0008736	ORPHA:93328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0008905	ORPHA:93328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93328	Autosomal dominant omodysplasia		HP:0010034	ORPHA:93328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0000343	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0000358	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0000369	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0000463	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0000944	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0002007	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0002818	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0003042	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0004322	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0005025	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0005280	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0008905	ORPHA:93329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0000028	ORPHA:93329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0000347	ORPHA:93329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0002823	ORPHA:93329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0002983	ORPHA:93329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0003027	ORPHA:93329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0001059	ORPHA:93329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0001249	ORPHA:93329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0001363	ORPHA:93329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0003196	ORPHA:93329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0010880	ORPHA:93329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0030680	ORPHA:93329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93329	Autosomal recessive omodysplasia		HP:0100790	ORPHA:93329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000028	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000218	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000316	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000347	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000358	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000426	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000520	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000581	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001249	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0002236	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0002553	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0002996	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0004322	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0009891	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0009911	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0010657	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0040064	ORPHA:221120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000023	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000085	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000202	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000238	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000256	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000268	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000286	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000322	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000324	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000337	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000387	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000602	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000691	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000767	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000884	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0000954	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001156	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001238	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001263	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001611	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001655	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001746	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001763	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001845	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0001864	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0002007	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0002033	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0002209	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0003186	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0003473	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0004442	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0004684	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0005048	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0006610	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0008598	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0008947	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0009739	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0009778	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0010044	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0010767	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0011470	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0025193	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0030043	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0040025	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0100259	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221120	Pseudoaminopterin syndrome		HP:0100759	ORPHA:221120	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000481	ORPHA:411634	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000083	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000093	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000114	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000531	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000613	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0001994	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0002013	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0003076	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0003126	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0003355	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0200026	ORPHA:411634	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000117	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0000821	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0001510	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0001959	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0002148	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0002900	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0002901	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0002902	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0002907	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0003259	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0003537	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0003774	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0004396	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0010639	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0012598	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0012622	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0032639	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0100512	ORPHA:411634	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0001250	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0001508	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0001942	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0001944	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0002750	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0003472	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0011106	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0011314	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411634	Juvenile nephropathic cystinosis		HP:0011968	ORPHA:411634	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0006495	ORPHA:93320	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009380	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0002758	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0002986	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0002996	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0003059	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0006433	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0005773	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0006055	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0040070	ORPHA:93320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0000882	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0001377	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0002650	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0002987	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0003041	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0003083	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0003316	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0003887	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0003967	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0005879	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0006376	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0006467	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0006633	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009164	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009238	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009281	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009471	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009701	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009702	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009760	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009813	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0009959	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0010011	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0010048	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0010176	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0010301	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0010331	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0030835	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0100558	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93320	Isolated ulnar hemimelia		HP:0100745	ORPHA:93320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93321	Isolated radial hemimelia		HP:0006501	ORPHA:93321	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:93321	Isolated radial hemimelia		HP:0001172	ORPHA:93321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93321	Isolated radial hemimelia		HP:0004243	ORPHA:93321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93321	Isolated radial hemimelia		HP:0004252	ORPHA:93321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93321	Isolated radial hemimelia		HP:0009484	ORPHA:93321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93321	Isolated radial hemimelia		HP:0010035	ORPHA:93321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0002199	ORPHA:93324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0002901	ORPHA:93324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0008198	ORPHA:93324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0000252	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0000270	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0000293	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0000316	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0000670	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0000883	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0001510	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0001511	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0001773	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0002750	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0003472	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0004331	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0005450	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0005791	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0006470	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0006645	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0008897	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0100254	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93324	Autosomal recessive Kenny-Caffey syndrome		HP:0200055	ORPHA:93324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0000270	ORPHA:93325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0004322	ORPHA:93325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0005791	ORPHA:93325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0100254	ORPHA:93325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0000316	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0000540	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0000670	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0001085	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0001510	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0001511	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0001903	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0002135	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0002199	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0002750	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0002905	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0003472	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0004331	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0005450	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0005490	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0006470	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0007633	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0007862	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0008198	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0008734	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0008897	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0011220	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0030346	ORPHA:93325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0000519	ORPHA:93325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0001620	ORPHA:93325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93325	Autosomal dominant Kenny-Caffey syndrome		HP:0006335	ORPHA:93325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0001762	ORPHA:93322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0009556	ORPHA:93322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0001171	ORPHA:93322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0004987	ORPHA:93322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0006380	ORPHA:93322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0001159	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0001385	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0001839	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0001840	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0001849	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0003974	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0006433	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0005736	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0005892	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0006426	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0006460	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0008368	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0010037	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0010043	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0010442	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0010554	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0012165	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0012386	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0030032	ORPHA:93322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0000028	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0000047	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0000062	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0000175	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0000365	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0002475	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0002673	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0002827	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93322	Isolated tibial hemimelia		HP:0002937	ORPHA:93322	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0001260	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0001272	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0002066	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0002080	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0002136	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0002194	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0001288	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0002359	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0002373	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0006855	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0007010	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0008936	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0012759	ORPHA:512260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0000639	ORPHA:512260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation		HP:0001410	ORPHA:512260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation	NOT	HP:0001273	ORPHA:512260	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:512260	Congenital cerebellar ataxia due to RNU12 mutation	NOT	HP:0002120	ORPHA:512260	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0030772	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0031058	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001288	ORPHA:93323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0002991	ORPHA:93323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001762	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0002857	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0002982	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0005736	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0006437	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0009826	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0040069	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0100559	ORPHA:93323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001376	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001387	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001382	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001770	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001772	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001831	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0002979	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0003038	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0003097	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0003184	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0003365	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0005085	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0006101	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0006460	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0010219	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0011849	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0012165	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0012531	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0030043	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0045086	ORPHA:93323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0000110	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0000478	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0000528	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0000593	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001249	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001363	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001627	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001849	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0001873	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0002414	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0002990	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0003274	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0040071	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0100257	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93323	Isolated fibular hemimelia		HP:0100656	ORPHA:93323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0000316	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0000348	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0000463	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0000637	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0002007	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0002566	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0002580	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508410	Familial intestinal malrotation		HP:0005280	ORPHA:508410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280785	Bullous diffuse cutaneous mastocytosis		HP:0000989	ORPHA:280785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280785	Bullous diffuse cutaneous mastocytosis		HP:0001019	ORPHA:280785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280785	Bullous diffuse cutaneous mastocytosis		HP:0001025	ORPHA:280785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280785	Bullous diffuse cutaneous mastocytosis		HP:0005587	ORPHA:280785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280785	Bullous diffuse cutaneous mastocytosis		HP:0006543	ORPHA:280785	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280785	Bullous diffuse cutaneous mastocytosis		HP:0008066	ORPHA:280785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280785	Bullous diffuse cutaneous mastocytosis		HP:0200151	ORPHA:280785	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0000044	ORPHA:1643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0000144	ORPHA:1643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0000147	ORPHA:1643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0000545	ORPHA:1643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0000869	ORPHA:1643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0000960	ORPHA:1643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0002916	ORPHA:1643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0004322	ORPHA:1643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0004397	ORPHA:1643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0007759	ORPHA:1643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0008056	ORPHA:1643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1643	Xp22.3 microdeletion syndrome		HP:0008065	ORPHA:1643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0000061	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0000063	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0000347	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0000786	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0003083	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0003871	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0007628	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0010650	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome		HP:0040253	ORPHA:2975	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome	NOT	HP:0000130	ORPHA:2975	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome	NOT	HP:0000137	ORPHA:2975	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2975	46,XX difference of sex development-skeletal anomalies syndrome	NOT	HP:0000142	ORPHA:2975	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000243	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000316	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000358	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000431	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000470	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000520	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000582	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0001249	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0001252	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0001263	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0002705	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0003196	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0008551	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0009738	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0011800	ORPHA:1642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000047	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000059	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000164	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000286	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0001156	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0006610	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0009906	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0011039	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0100625	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0100790	ORPHA:1642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0000175	ORPHA:1642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1642	Distal deletion 9p syndrome		HP:0030680	ORPHA:1642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0003310	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0004979	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0006505	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0007517	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0007574	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0008788	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0010864	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0012767	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0430005	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0430028	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:3000077	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0010819	ORPHA:2976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0012412	ORPHA:2976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0030348	ORPHA:2976	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type	NOT	HP:0001511	ORPHA:2976	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0000015	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0000400	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0000448	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0000819	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0001007	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0001176	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0001386	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0001833	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0002069	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0002684	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0002750	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0002751	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0002857	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2976	Pseudoleprechaunism syndrome, Patterson type		HP:0003180	ORPHA:2976	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2978	Chronic intestinal pseudoobstruction syndrome		HP:0001643	ORPHA:2978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2978	Chronic intestinal pseudoobstruction syndrome		HP:0002021	ORPHA:2978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2978	Chronic intestinal pseudoobstruction syndrome		HP:0002242	ORPHA:2978	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2978	Chronic intestinal pseudoobstruction syndrome		HP:0002566	ORPHA:2978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2978	Chronic intestinal pseudoobstruction syndrome		HP:0011875	ORPHA:2978	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2978	Chronic intestinal pseudoobstruction syndrome		HP:0012639	ORPHA:2978	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002518	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002828	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0007204	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0007301	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0012332	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001272	ORPHA:466934	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy	NOT	HP:0000280	ORPHA:466934	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy	NOT	HP:0001433	ORPHA:466934	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0000252	ORPHA:466934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001249	ORPHA:466934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001250	ORPHA:466934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001252	ORPHA:466934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001263	ORPHA:466934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0100704	ORPHA:466934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0000011	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0000407	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0000648	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001257	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001344	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0001510	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002019	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002079	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002119	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002188	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002373	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466934	VPS11-related autosomal recessive hypomyelinating leukodystrophy		HP:0002465	ORPHA:466934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0000510	ORPHA:436274	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0000662	ORPHA:436274	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0000973	ORPHA:436274	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0000486	ORPHA:436274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0000587	ORPHA:436274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0001582	ORPHA:436274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0007522	ORPHA:436274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0007843	ORPHA:436274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0007980	ORPHA:436274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0200034	ORPHA:436274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436274	Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa		HP:0001098	ORPHA:436274	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0000044	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0000047	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0000135	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0000238	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0000568	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0000589	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0000823	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0001249	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0001513	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0004322	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0005321	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141333	Biemond syndrome type 2		HP:0100258	ORPHA:141333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0001945	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0002014	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0002027	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0002573	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0002607	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0012701	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0012702	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0032155	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0032168	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217067	Pouchitis		HP:0500005	ORPHA:217067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0006980	ORPHA:436271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0007133	ORPHA:436271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0000093	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0000124	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0000508	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0000580	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0000648	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0000750	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001249	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001250	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001251	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001262	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001263	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001270	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001288	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001290	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001410	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001508	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001639	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001903	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001994	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0002240	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0002376	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0002490	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0002747	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0002875	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0003076	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0003109	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0003128	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0003324	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0003355	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0006555	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0007256	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0008619	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0030195	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0040291	ORPHA:436271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0001285	ORPHA:436271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436271	Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy		HP:0002013	ORPHA:436271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000003	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000010	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000014	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000028	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000069	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000072	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000076	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000083	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000130	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000144	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000767	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0000772	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001374	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001508	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001562	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001629	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001631	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001636	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001643	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0001762	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0002019	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0002023	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0002205	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0002566	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0002580	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0002650	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0003422	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0005199	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0006703	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0008734	ORPHA:2970	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0010957	ORPHA:2970	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0011100	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0100543	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2970	Prune belly syndrome		HP:0100779	ORPHA:2970	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0007489	ORPHA:280779	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0000967	ORPHA:280779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0000978	ORPHA:280779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0000988	ORPHA:280779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0007394	ORPHA:280779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0010783	ORPHA:280779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0011276	ORPHA:280779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0012733	ORPHA:280779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0001939	ORPHA:280779	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280779	Cutaneous collagenous vasculopathy		HP:0000989	ORPHA:280779	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001256	ORPHA:314647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001263	ORPHA:314647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000179	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000276	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000307	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000343	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000414	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000445	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000463	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000486	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000490	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000718	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000729	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000750	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001251	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001260	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001310	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001319	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001321	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002019	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002317	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002354	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002470	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002536	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0011166	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0012433	ORPHA:314647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000160	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0000256	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0001348	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002003	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002080	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0002120	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0007256	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0011067	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0025517	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0100540	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability		HP:0400005	ORPHA:314647	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability	NOT	HP:0000639	ORPHA:314647	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability	NOT	HP:0002403	ORPHA:314647	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000286	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000316	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000369	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000407	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000486	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000512	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000545	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000639	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000648	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000649	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0000668	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001161	ORPHA:2971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001250	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001252	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001263	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001276	ORPHA:2971	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001288	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001347	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001508	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001522	ORPHA:2971	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0001939	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0002093	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0002167	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0002240	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0002353	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0002376	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0005280	ORPHA:2971	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0010864	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2971	Peroxisomal acyl-CoA oxidase deficiency		HP:0012639	ORPHA:2971	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000028	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000154	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000202	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000238	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000316	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000365	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000384	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000508	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000612	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000625	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000639	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000772	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000776	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000921	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001053	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001161	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001231	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001249	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001250	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001260	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001305	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001321	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001362	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001374	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001596	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0001883	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0002006	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0002119	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0002126	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0002334	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0004374	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0006101	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0007370	ORPHA:1647	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0007957	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0008065	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0000377	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0009882	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0010185	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0010609	ORPHA:1647	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1647	Oculocerebrocutaneous syndrome		HP:0100777	ORPHA:1647	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0000272	ORPHA:2972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0000358	ORPHA:2972	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0000668	ORPHA:2972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0000684	ORPHA:2972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0002857	ORPHA:2972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0005439	ORPHA:2972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0006329	ORPHA:2972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2972	Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome		HP:0006482	ORPHA:2972	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1646	Chromosome Y microdeletion syndrome		HP:0003251	ORPHA:1646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1646	Chromosome Y microdeletion syndrome		HP:0008669	ORPHA:1646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1646	Chromosome Y microdeletion syndrome		HP:0008734	ORPHA:1646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1646	Chromosome Y microdeletion syndrome		HP:0011961	ORPHA:1646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1646	Chromosome Y microdeletion syndrome		HP:0000798	ORPHA:1646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1646	Chromosome Y microdeletion syndrome		HP:0000028	ORPHA:1646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0000003	ORPHA:2973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0000072	ORPHA:2973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0000126	ORPHA:2973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0000795	ORPHA:2973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0000812	ORPHA:2973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0001562	ORPHA:2973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0002023	ORPHA:2973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0002093	ORPHA:2973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0002566	ORPHA:2973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0002575	ORPHA:2973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0006501	ORPHA:2973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0008678	ORPHA:2973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0010458	ORPHA:2973	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0100627	ORPHA:2973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2973	46,XX difference of sex development-anorectal anomalies syndrome		HP:0100779	ORPHA:2973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0000775	ORPHA:505395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0005946	ORPHA:505395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0009113	ORPHA:505395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0025464	ORPHA:505395	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0003457	ORPHA:505395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0012496	ORPHA:505395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0032169	ORPHA:505395	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0000821	ORPHA:505395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0002747	ORPHA:505395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0011458	ORPHA:505395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0012416	ORPHA:505395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0032341	ORPHA:505395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0100806	ORPHA:505395	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505395	Ventilator-induced diaphragmatic dysfunction		HP:0006597	ORPHA:505395	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280794	Pseudoxanthomatous diffuse cutaneous mastocytosis		HP:0008066	ORPHA:280794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280794	Pseudoxanthomatous diffuse cutaneous mastocytosis		HP:0200151	ORPHA:280794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000388	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000750	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000943	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001249	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001328	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002719	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002721	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0010471	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0011842	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0012379	ORPHA:309282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000280	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000316	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000410	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000486	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000518	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000540	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000545	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000736	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001251	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001252	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001256	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001270	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001433	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002090	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0003198	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0011334	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0025406	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0031123	ORPHA:309282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000158	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000248	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000256	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000297	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000303	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000337	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000407	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000470	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000483	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000520	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000543	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000687	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000708	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000716	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000738	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000739	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000746	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000767	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000768	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000900	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000926	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000938	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000977	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001258	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001272	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001289	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001363	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001387	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001382	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001519	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001537	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001653	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001776	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001876	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002120	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002308	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002312	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002329	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002553	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002679	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002684	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002797	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002857	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0004437	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0004684	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0005280	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0005791	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0007957	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0008821	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0008936	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0010665	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0010885	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0011220	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0012157	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0012368	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0430022	ORPHA:309282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0000010	ORPHA:309282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001334	ORPHA:309282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0001659	ORPHA:309282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309282	Alpha-mannosidosis, infantile form		HP:0002371	ORPHA:309282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0011771	ORPHA:36913	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002901	ORPHA:36913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002905	ORPHA:36913	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0000518	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002150	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0003401	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0030057	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0031817	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0031990	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0033748	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:6000919	ORPHA:36913	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0000509	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0000716	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0000737	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0000738	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0000739	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0001265	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0001289	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0001596	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0001657	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002071	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002094	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002135	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002728	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002960	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0003394	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0003472	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0003739	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0004724	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0011001	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0011458	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0012049	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0025425	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0100749	ORPHA:36913	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0001677	ORPHA:36913	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0002199	ORPHA:36913	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0004308	ORPHA:36913	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:36913	Autoimmune hypoparathyroidism		HP:0005162	ORPHA:36913	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0001256	ORPHA:309288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0010471	ORPHA:309288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0001251	ORPHA:309288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0002719	ORPHA:309288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0025406	ORPHA:309288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000158	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000410	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000518	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000545	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000708	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000716	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000738	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000739	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000746	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000750	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000938	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0001272	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0001289	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0001433	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0002090	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0002120	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0002312	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0002329	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0002721	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0012157	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0031123	ORPHA:309288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0000543	ORPHA:309288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0001659	ORPHA:309288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0001876	ORPHA:309288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309288	Alpha-mannosidosis, adult form		HP:0007957	ORPHA:309288	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2964	Autosomal dominant prognathism		HP:0000232	ORPHA:2964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2964	Autosomal dominant prognathism		HP:0000303	ORPHA:2964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2964	Autosomal dominant prognathism		HP:0010807	ORPHA:2964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000026	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000044	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000134	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000135	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000140	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000141	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000802	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000858	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000868	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0012041	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0012503	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0030018	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0100639	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0100829	ORPHA:2965	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000529	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000771	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000938	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000939	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000980	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0002013	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0002017	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0002315	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0002615	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0002920	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0003388	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0008240	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0008245	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0011362	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0011734	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0011735	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0011748	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0012378	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0030016	ORPHA:2965	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000508	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000618	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000651	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000823	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000830	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0000845	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0001117	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0001250	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0002321	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0006824	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0006897	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0007011	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0007942	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0012246	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0012377	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0030517	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2965	Prolactinoma		HP:0030521	ORPHA:2965	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0005528	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0006527	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0007499	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0009098	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0011107	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0011947	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0032434	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0032435	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000099	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000164	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000166	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000246	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000280	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000509	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000717	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000825	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001249	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001250	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001287	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001510	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001892	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001894	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001901	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0002059	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0002110	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0002754	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0003540	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0004322	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0005575	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0008404	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0009789	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0011110	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0020087	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0025452	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0030683	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0100806	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0500035	ORPHA:2968	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000252	ORPHA:2968	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001511	ORPHA:2968	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0004440	ORPHA:2968	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0004808	ORPHA:2968	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0002718	ORPHA:2968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0011990	ORPHA:2968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0040238	ORPHA:2968	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000010	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000230	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0000388	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001581	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0001974	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0002090	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0002586	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2968	Leukocyte adhesion deficiency		HP:0002841	ORPHA:2968	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000147	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000238	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000256	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000268	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000303	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000463	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000494	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000518	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000541	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000545	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000615	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0000828	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0001028	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0001031	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0001100	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0001140	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0001249	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0001334	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0001744	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0002652	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0002816	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0005293	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0007400	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0009721	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0010516	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0010807	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0010816	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0100559	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0100730	ORPHA:2969	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0100774	ORPHA:2969	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2969	Proteus-like syndrome		HP:0100777	ORPHA:2969	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0003549	ORPHA:217059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0001500	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0001795	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0001805	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0001821	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0001837	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0002164	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0011300	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0011304	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0100759	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0100760	ORPHA:217059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0008391	ORPHA:217059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing		HP:0012203	ORPHA:217059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing	NOT	HP:0000951	ORPHA:217059	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing	NOT	HP:0000975	ORPHA:217059	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing	NOT	HP:0002653	ORPHA:217059	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:217059	Isolated nail clubbing	NOT	HP:0002829	ORPHA:217059	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000750	ORPHA:466926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0001250	ORPHA:466926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0001263	ORPHA:466926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0004349	ORPHA:466926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000028	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000077	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000256	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000316	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000343	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000356	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000414	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000717	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000951	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0001252	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0001256	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0001845	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0002018	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0002019	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0002020	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0002136	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0002342	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0002650	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0030680	ORPHA:466926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000252	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0000348	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0001561	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0001631	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0004425	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0010864	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0011220	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466926	Seizures-scoliosis-macrocephaly syndrome		HP:0100777	ORPHA:466926	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000252	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000293	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000347	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000414	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000470	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000582	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0001252	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0001276	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0002683	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0004322	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0006889	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0007598	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0008736	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0010978	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0012368	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0100729	ORPHA:1636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000028	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000154	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000175	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000400	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000486	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0001250	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0001360	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0100335	ORPHA:1636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000648	ORPHA:1636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0000767	ORPHA:1636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0004209	ORPHA:1636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0006610	ORPHA:1636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0009773	ORPHA:1636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1636	Distal monosomy 7q36 syndrome		HP:0100790	ORPHA:1636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001611	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001762	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001788	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001884	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0002305	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0002645	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0002750	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0002751	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0002761	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0002812	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0003199	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0004322	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0005272	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0005328	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0005425	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0007457	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0007957	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0008070	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0008897	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0008947	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0009125	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0009748	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0010648	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0011003	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0011220	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0025167	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0200141	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000518	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000592	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001273	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001320	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001629	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0002073	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0007392	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0030604	ORPHA:2962	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000028	ORPHA:2962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001643	ORPHA:2962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0005301	ORPHA:2962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0008619	ORPHA:2962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0012304	ORPHA:2962	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome	NOT	HP:0002097	ORPHA:2962	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000023	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000160	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000218	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000248	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000253	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000286	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000316	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000369	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000490	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000494	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000684	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000750	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000767	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000938	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000963	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0000973	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001181	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001263	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001347	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001374	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001476	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001508	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001511	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001537	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2962	De Barsy syndrome		HP:0001558	ORPHA:2962	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000232	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000260	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000286	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000303	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000337	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000358	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000486	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000574	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0000973	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0001508	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0001511	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0001537	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0001582	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0001595	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0001597	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0002230	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0002299	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0003758	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0004322	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0004331	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0007477	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0007495	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0007740	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0008070	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0009721	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0009804	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0009882	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2963	Progeroid syndrome, Petty type		HP:0100578	ORPHA:2963	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0002063	ORPHA:314632	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0001332	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0001336	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0001337	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0002067	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0002172	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0002506	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0002548	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0003487	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0025331	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0100543	ORPHA:314632	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0001260	ORPHA:314632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0001288	ORPHA:314632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0001324	ORPHA:314632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0002339	ORPHA:314632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0012378	ORPHA:314632	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0000716	ORPHA:314632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314632	CLN12 disease		HP:0002174	ORPHA:314632	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000648	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000712	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000726	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000736	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000738	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000746	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000762	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001260	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001265	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001290	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001324	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001332	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002312	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002354	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001288	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002359	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002376	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002415	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002922	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0004343	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0012433	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0030081	ORPHA:309271	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000020	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000649	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0000716	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001082	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001257	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001939	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002072	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002080	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002371	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002478	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002483	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0002607	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0003270	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0003444	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0003487	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0007133	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0007240	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0007272	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0007663	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0008619	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0100753	ORPHA:309271	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0001250	ORPHA:309271	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0004926	ORPHA:309271	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0025013	ORPHA:309271	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0031358	ORPHA:309271	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309271	Metachromatic leukodystrophy, adult form		HP:0100575	ORPHA:309271	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35612	Nanophthalmos		HP:0000486	ORPHA:35612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35612	Nanophthalmos		HP:0000501	ORPHA:35612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35612	Nanophthalmos		HP:0000568	ORPHA:35612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35612	Nanophthalmos		HP:0000610	ORPHA:35612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35612	Nanophthalmos		HP:0007703	ORPHA:35612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35612	Nanophthalmos		HP:0008499	ORPHA:35612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000028	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000079	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000235	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000256	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000286	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000316	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000343	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000431	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000463	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000470	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0000774	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0001155	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0001252	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0001274	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0001387	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0006610	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1621	3q13 microdeletion syndrome		HP:0008736	ORPHA:1621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000028	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000160	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000218	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000219	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000239	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000316	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000343	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000358	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000400	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000411	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000494	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000592	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000766	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000974	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000978	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001075	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001238	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001324	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001519	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001892	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001933	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002194	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002650	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002761	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002804	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0003196	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0003199	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0003319	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0005272	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0006184	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000377	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0012534	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0031869	ORPHA:2953	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000308	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000483	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000486	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000541	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000545	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001182	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001581	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001582	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002019	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002751	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002947	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0003198	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0007906	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0430043	ORPHA:2953	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000009	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000126	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000175	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000365	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000501	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000787	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001363	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001627	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0001654	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002107	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0002119	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0003414	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0100016	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0410030	ORPHA:2953	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000023	ORPHA:2953	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0000085	ORPHA:2953	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2953	Musculocontractural Ehlers-Danlos syndrome		HP:0004794	ORPHA:2953	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000023	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000028	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000175	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000218	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000233	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000248	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000252	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000286	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000316	ORPHA:1620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000325	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000343	ORPHA:1620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000347	ORPHA:1620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000365	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000358	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000463	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000470	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000506	ORPHA:1620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000508	ORPHA:1620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000581	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0000960	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0001162	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0001250	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0001252	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0001257	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0001511	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0001537	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0002119	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0002714	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0004209	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0004322	ORPHA:1620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0004467	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0006695	ORPHA:1620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0007670	ORPHA:1620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1620	Distal deletion 3p syndrome		HP:0100543	ORPHA:1620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2956	Acrodysplasia scoliosis		HP:0001156	ORPHA:2956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2956	Acrodysplasia scoliosis		HP:0002650	ORPHA:2956	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2956	Acrodysplasia scoliosis		HP:0003298	ORPHA:2956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2956	Acrodysplasia scoliosis		HP:0003422	ORPHA:2956	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000219	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000252	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000341	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000426	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000455	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001263	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001319	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001999	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0002465	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0010864	ORPHA:457193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000286	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000308	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000358	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000486	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000508	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001250	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001357	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001363	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001510	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001629	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001631	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001643	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0002020	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0002643	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0002714	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0003552	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0004322	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0011968	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0100704	ORPHA:457193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000028	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000126	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000175	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0000648	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001156	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001332	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0001601	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0002566	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0004467	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457193	KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome		HP:0007678	ORPHA:457193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000023	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000028	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000278	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000286	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000316	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000348	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000369	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000448	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000486	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000508	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000639	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0000939	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0001098	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0001249	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0001290	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0001776	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0002059	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0002673	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0005815	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0010499	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0010781	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0011064	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2958	X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome		HP:0040019	ORPHA:2958	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000047	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000054	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000193	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000252	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000320	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000347	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000408	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000518	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000529	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000585	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000668	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000689	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000815	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000823	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000831	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0000938	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001156	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001397	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001518	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001592	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001596	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001620	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002020	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002136	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002162	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002360	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002721	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002828	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002910	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0003401	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0003808	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0004322	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0004429	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0005115	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0005320	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0005328	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0005403	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0007481	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0007495	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0008209	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0008214	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0009882	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0010536	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0010663	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0025124	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0040171	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0100543	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0100785	ORPHA:2959	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001256	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001270	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0001935	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002572	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002664	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002894	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0002943	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2959	Progeria-short stature-pigmented nevi syndrome		HP:0040160	ORPHA:2959	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:243343	Dimethylglycine dehydrogenase deficiency		HP:0001939	ORPHA:243343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243343	Dimethylglycine dehydrogenase deficiency		HP:0003236	ORPHA:243343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243343	Dimethylglycine dehydrogenase deficiency		HP:0003750	ORPHA:243343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243343	Dimethylglycine dehydrogenase deficiency		HP:0012379	ORPHA:243343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:243343	Dimethylglycine dehydrogenase deficiency		HP:0410020	ORPHA:243343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0001627	ORPHA:1627	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0000239	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0000256	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0000286	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0000316	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0000470	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0000768	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0001252	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0001270	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0001531	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0002557	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0002751	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0008897	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1627	Deletion 5q35 syndrome		HP:0010880	ORPHA:1627	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000154	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000157	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000175	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000244	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000252	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000278	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000316	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000365	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000470	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0000742	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0001263	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0001274	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0001561	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0002061	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0002084	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0002418	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0002679	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0002943	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0003310	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0003319	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0004322	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0004325	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0007036	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0007642	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0009792	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0010864	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0011069	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0011729	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0011800	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0012286	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0012503	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0100872	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:3000005	ORPHA:314621	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314621	Duplication of the pituitary gland		HP:0002580	ORPHA:314621	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000020	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000648	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000736	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000762	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001260	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001265	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001290	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001324	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001332	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0002312	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0002359	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0002376	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0002415	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0002922	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0004343	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0012433	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0030081	ORPHA:309263	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000649	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000712	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000738	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0000746	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001082	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001250	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001257	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0001939	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0002080	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0002371	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0003270	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0003444	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0003487	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0007133	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0007240	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0007272	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0007663	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0008619	ORPHA:309263	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0025013	ORPHA:309263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309263	Metachromatic leukodystrophy, juvenile form		HP:0031358	ORPHA:309263	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0001324	ORPHA:2942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0012531	ORPHA:2942	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0002829	ORPHA:2942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0003326	ORPHA:2942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0003551	ORPHA:2942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0011446	ORPHA:2942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0012378	ORPHA:2942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0100786	ORPHA:2942	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0001260	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0001367	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0002015	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0002093	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0002360	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0002380	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0003202	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0003394	ORPHA:2942	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2942	Postpoliomyelitis syndrome		HP:0002791	ORPHA:2942	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:48918	Focal myositis		HP:0001324	ORPHA:48918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48918	Focal myositis		HP:0001376	ORPHA:48918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48918	Focal myositis		HP:0001824	ORPHA:48918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48918	Focal myositis		HP:0001945	ORPHA:48918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48918	Focal myositis		HP:0003236	ORPHA:48918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48918	Focal myositis		HP:0003326	ORPHA:48918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48918	Focal myositis		HP:0100614	ORPHA:48918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0000016	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0000112	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0000501	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0000802	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0000970	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0001097	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0001635	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0001712	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0001723	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0002014	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0002017	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0002019	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0002578	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0003202	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0004926	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0007141	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0011675	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0012185	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0012332	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0012722	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0031327	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0100832	ORPHA:271861	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0000083	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0000100	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0001324	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0001824	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0004610	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0009027	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0010829	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0011970	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0012531	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0025309	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0031006	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0031189	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0033748	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:271861	Hereditary ATTR amyloidosis		HP:0100550	ORPHA:271861	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000175	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000190	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000274	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000316	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000322	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000358	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000470	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000494	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000525	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000568	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000589	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000518	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000708	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0000729	ORPHA:1617	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001263	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001188	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001249	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001250	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001319	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001510	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001508	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001518	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0001770	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0002871	ORPHA:1617	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0010078	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0011344	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0100490	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1617	Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to 2q24 microdeletion		HP:0100807	ORPHA:1617	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0000238	ORPHA:163596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0000980	ORPHA:163596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0001561	ORPHA:163596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0001562	ORPHA:163596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0001635	ORPHA:163596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0001701	ORPHA:163596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0001744	ORPHA:163596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0001789	ORPHA:163596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0001903	ORPHA:163596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0002240	ORPHA:163596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0011902	ORPHA:163596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163596	Hb Bart's hydrops fetalis		HP:0100602	ORPHA:163596	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0001249	ORPHA:2940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0001250	ORPHA:2940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0001257	ORPHA:2940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0002119	ORPHA:2940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0002132	ORPHA:2940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0004374	ORPHA:2940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0100021	ORPHA:2940	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2940	Porencephaly		HP:0100022	ORPHA:2940	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0003755	ORPHA:596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0030917	ORPHA:596	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0000478	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0001319	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0001558	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0001561	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0001622	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0002033	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0002090	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0002098	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0002205	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0003687	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0004887	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0006829	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0008872	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0030192	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0030195	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0030319	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0031238	ORPHA:596	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0000218	ORPHA:596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0000268	ORPHA:596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0000276	ORPHA:596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0001999	ORPHA:596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:596	X-linked centronuclear myopathy		HP:0002540	ORPHA:596	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0003198	ORPHA:598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0003560	ORPHA:598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0003789	ORPHA:598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0000486	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0001290	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0001387	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0001508	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0002093	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0002650	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0002747	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0003306	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0003457	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0004303	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0004322	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0001382	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0008994	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0008997	ORPHA:598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0000544	ORPHA:598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0002047	ORPHA:598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0002460	ORPHA:598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:598	Multiminicore myopathy		HP:0002804	ORPHA:598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001252	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001270	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001374	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001382	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001634	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001762	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001763	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0002047	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0002751	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0002828	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0003198	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0003388	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0003552	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0003749	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0003803	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0030230	ORPHA:597	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0000602	ORPHA:597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0002483	ORPHA:597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0003798	ORPHA:597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0040081	ORPHA:597	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0001989	ORPHA:597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0002643	ORPHA:597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0002747	ORPHA:597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease		HP:0003236	ORPHA:597	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:597	Central core disease	NOT	HP:0040191	ORPHA:597	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:592	Macrophagic myofasciitis		HP:0001945	ORPHA:592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:592	Macrophagic myofasciitis		HP:0002829	ORPHA:592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:592	Macrophagic myofasciitis		HP:0003324	ORPHA:592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:592	Macrophagic myofasciitis		HP:0003326	ORPHA:592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:592	Macrophagic myofasciitis		HP:0003457	ORPHA:592	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592	Macrophagic myofasciitis		HP:0012378	ORPHA:592	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0000221	ORPHA:2928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0000762	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0001156	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0001249	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0001288	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0001315	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0001324	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0001956	ORPHA:2928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0002644	ORPHA:2928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0002983	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0003457	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0004322	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0009465	ORPHA:2928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0011675	ORPHA:2928	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0100490	ORPHA:2928	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2928	Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome		HP:0008209	ORPHA:2928	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0005266	ORPHA:2929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0012198	ORPHA:2929	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0100896	ORPHA:2929	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0004784	ORPHA:2929	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0004795	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002573	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0001903	ORPHA:2929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002027	ORPHA:2929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002576	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002014	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0100822	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0001510	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000969	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002239	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0012432	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002243	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000256	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0001012	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0010797	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0001999	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002003	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000316	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000494	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0005280	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000369	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000160	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000331	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0001256	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0004406	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0100579	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0100761	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002326	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0030049	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0004941	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002092	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0003003	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0012126	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002894	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0100833	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0004390	ORPHA:2929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0030256	ORPHA:2929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0001508	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0012050	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0003075	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0000421	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0100026	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0100759	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0006548	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0006574	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0002408	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0040231	ORPHA:2929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2929	Juvenile polyposis syndrome		HP:0007378	ORPHA:2929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000467	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000508	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002015	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002033	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002882	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003473	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003701	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0004661	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0004889	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0011968	ORPHA:590	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000602	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000961	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001249	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001251	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001283	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001558	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001611	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002205	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001288	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002804	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002872	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003324	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003388	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0004885	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0008443	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0010536	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0011469	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0030842	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0100285	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0100295	ORPHA:590	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000218	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000276	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001250	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001252	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001270	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001284	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001612	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001618	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001761	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002421	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002515	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002751	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003306	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003325	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003458	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0003693	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0009053	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0010307	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0012801	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0030051	ORPHA:590	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000308	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000369	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000407	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000565	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000639	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000651	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0000768	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001265	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001374	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001382	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0001561	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002020	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002392	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0002870	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0005943	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0007178	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome		HP:0025401	ORPHA:590	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:590	Congenital myasthenic syndrome	NOT	HP:0030208	ORPHA:590	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002748	ORPHA:289157	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002901	ORPHA:289157	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0012052	ORPHA:289157	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0000867	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0000886	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0000897	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0000920	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001270	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001281	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001324	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001508	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002148	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002653	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002659	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002663	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002749	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002752	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002753	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002909	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002970	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002980	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002982	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0003020	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0003029	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0003106	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0003165	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0005042	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0005469	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0008897	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0010537	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0010639	ORPHA:289157	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001290	ORPHA:289157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001638	ORPHA:289157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001931	ORPHA:289157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002007	ORPHA:289157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001288	ORPHA:289157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0003155	ORPHA:289157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0004322	ORPHA:289157	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0000684	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0000737	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001538	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001744	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0001974	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002199	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0002240	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289157	Hypocalcemic vitamin D-dependent rickets		HP:0006297	ORPHA:289157	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0000762	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0001284	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0002317	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0003401	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0003474	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0003481	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0009830	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0010871	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0011096	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0012078	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0030200	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0040129	ORPHA:2932	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0001288	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0002527	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0003551	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0030237	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0034135	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0034136	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0034137	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0034138	ORPHA:2932	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2932	Chronic inflammatory demyelinating polyneuropathy		HP:0010833	ORPHA:2932	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464318	Verrucous hemangioma		HP:0001028	ORPHA:464318	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:464318	Verrucous hemangioma		HP:0011123	ORPHA:464318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464318	Verrucous hemangioma		HP:0011356	ORPHA:464318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464318	Verrucous hemangioma		HP:0012740	ORPHA:464318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464318	Verrucous hemangioma		HP:0025092	ORPHA:464318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464318	Verrucous hemangioma		HP:0045059	ORPHA:464318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464318	Verrucous hemangioma		HP:0200035	ORPHA:464318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0001159	ORPHA:2934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0001627	ORPHA:2934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0010442	ORPHA:2934	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000316	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000347	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000369	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000414	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000463	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0001561	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0001629	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0001631	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0006563	ORPHA:2934	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000286	ORPHA:2934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000518	ORPHA:2934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000568	ORPHA:2934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0000803	ORPHA:2934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0001636	ORPHA:2934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2934	Polysyndactyly-cardiac malformation syndrome		HP:0007902	ORPHA:2934	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0000288	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0000356	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0000364	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0000486	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0000582	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0001162	ORPHA:2935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0005280	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0006101	ORPHA:2935	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0007477	ORPHA:2935	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0008736	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2935	Crossed polysyndactyly		HP:0009601	ORPHA:2935	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000307	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000343	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000431	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000490	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000750	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001156	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001249	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001252	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001263	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001274	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001288	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001344	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001508	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001773	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002119	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002120	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002167	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002353	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002465	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0011228	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0011800	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0100490	ORPHA:1606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000160	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000248	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000252	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000270	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000286	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000358	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000457	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000486	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000504	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000534	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000708	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000717	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000733	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001250	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002015	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002019	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002020	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0004209	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0005280	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0008499	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0008872	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0030680	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0100716	ORPHA:1606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000028	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000047	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000055	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000077	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000107	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000126	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000135	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000405	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000407	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000464	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000505	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000518	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000639	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000648	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000821	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000878	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000892	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0000902	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001009	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001107	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001385	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001387	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001392	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001397	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001513	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001636	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001643	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001644	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001654	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001671	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001734	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001743	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0001829	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002007	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002021	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002230	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002242	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002591	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002650	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002715	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0002808	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0003006	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0003198	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0003416	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0004322	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0004374	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0004378	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0005113	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0006824	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0008066	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0008551	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0008736	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0012733	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1606	1p36 deletion syndrome		HP:0100559	ORPHA:1606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001324	ORPHA:589	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000508	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000597	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000651	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000777	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001260	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001283	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001618	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0002015	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0002094	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0003202	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0003551	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0003690	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0010516	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0012378	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0030006	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0030197	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0030208	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0030210	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0030319	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0100614	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:5000038	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:5000047	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:5000048	ORPHA:589	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000365	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000836	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000872	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001370	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0002725	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0002878	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0003076	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0003401	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0008207	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0010780	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0012473	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0030880	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0100522	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:5000046	ORPHA:589	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0000709	ORPHA:589	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001063	ORPHA:589	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001250	ORPHA:589	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0001878	ORPHA:589	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0012115	ORPHA:589	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:589	Myasthenia gravis		HP:0012410	ORPHA:589	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0000238	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0000486	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0000501	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0000505	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0000518	ORPHA:588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0000545	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0000648	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0001250	ORPHA:588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0001252	ORPHA:588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0001276	ORPHA:588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0001288	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0001360	ORPHA:588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0001608	ORPHA:588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0002167	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0002353	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0002435	ORPHA:588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0003198	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0003236	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0003457	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0004374	ORPHA:588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0007360	ORPHA:588	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0100022	ORPHA:588	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:588	Muscle-eye-brain disease		HP:0100543	ORPHA:588	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000252	ORPHA:464311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000708	ORPHA:464311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000750	ORPHA:464311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001249	ORPHA:464311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001263	ORPHA:464311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001999	ORPHA:464311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0011968	ORPHA:464311	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000504	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000729	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000733	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000739	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001250	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001270	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001288	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001344	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001508	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001511	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001518	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002119	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002120	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0003561	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0009121	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0410263	ORPHA:464311	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000341	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000411	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000426	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000483	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000486	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000490	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000540	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000543	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000545	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000577	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000646	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000767	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001182	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001773	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001831	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002013	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002020	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002079	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002363	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002650	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002719	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002808	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0003319	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0006466	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0007018	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0007957	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0011171	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0011757	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0012785	ORPHA:464311	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000028	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000047	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000054	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000107	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000122	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000125	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000126	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0000541	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001561	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001562	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001629	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001643	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001650	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0001659	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002247	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464311	Intellectual disability syndrome due to a DYRK1A point mutation		HP:0002269	ORPHA:464311	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0000221	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0000224	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0000256	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0000518	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001000	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001004	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001182	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001231	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001250	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001596	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001744	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001800	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001810	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0001903	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002014	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002024	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002027	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002039	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002231	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002232	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002240	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002597	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002664	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0002672	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0003003	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0004326	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0004390	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0007440	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0008391	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0012126	ORPHA:2930	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0012378	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0100840	ORPHA:2930	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2930	Cronkhite-Canada syndrome		HP:0200008	ORPHA:2930	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000054	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000303	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000400	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000479	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000545	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001018	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001166	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001182	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001249	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001256	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001263	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001319	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001510	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001643	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001762	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001763	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001999	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0002311	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0002714	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0002750	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0002751	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0004322	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0005148	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0005280	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0007204	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0008240	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0008513	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0008689	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0012447	ORPHA:1600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000154	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000194	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000218	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000238	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000252	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000286	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000294	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000322	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000407	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000414	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000448	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000452	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000486	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000494	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000767	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0000821	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001250	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001266	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001321	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001382	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001508	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001533	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001635	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001650	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001653	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0001684	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0002720	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0004422	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0004942	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0005134	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0005164	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0011596	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0012382	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0012471	ORPHA:1600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0003413	ORPHA:1600	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1600	Monosomy 18q syndrome		HP:0009592	ORPHA:1600	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000238	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000252	ORPHA:585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000256	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000280	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000319	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000407	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000463	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000505	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000518	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000574	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0000648	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0001249	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0001250	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0001263	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0001319	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0001387	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0001744	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0002208	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0002240	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0002376	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0003134	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0004322	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0005280	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0007307	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0007703	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0007957	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0008064	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0008155	ORPHA:585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0010059	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:585	Multiple sulfatase deficiency		HP:0011304	ORPHA:585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0000023	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0000280	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0000470	ORPHA:584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001004	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001249	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001252	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001387	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001537	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001541	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001744	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001789	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0001840	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0002103	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0002205	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0002650	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0003272	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0004607	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0005019	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0007957	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0008155	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0008430	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0010655	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0012115	ORPHA:584	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0012368	ORPHA:584	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0100026	ORPHA:584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:584	Mucopolysaccharidosis type 7		HP:0100625	ORPHA:584	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:281201	Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome		HP:0000982	ORPHA:281201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:281201	Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome		HP:0008064	ORPHA:281201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0001738	ORPHA:586	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002024	ORPHA:586	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002110	ORPHA:586	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002205	ORPHA:586	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0006536	ORPHA:586	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0012236	ORPHA:586	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0012873	ORPHA:586	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0001508	ORPHA:586	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0003251	ORPHA:586	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0000246	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0000716	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0000739	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0000938	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0001392	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002020	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002035	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002099	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002570	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002724	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002726	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002783	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002910	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0004401	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0005376	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0032342	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0045082	ORPHA:586	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0000365	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0000787	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0000939	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0001394	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002105	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002107	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0002842	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0032261	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:586	Cystic fibrosis		HP:0100582	ORPHA:586	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000023	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000365	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000389	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000518	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000545	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000772	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000889	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001250	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001251	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001276	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001385	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001387	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001537	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001604	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001744	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002024	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002208	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002230	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002240	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002360	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002376	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002650	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002857	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0003312	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0004493	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001249	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0007957	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0008155	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0010864	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001646	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001999	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001633	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001637	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0007256	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0025160	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0011842	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000164	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0004452	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000718	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0011951	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001678	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0005743	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000618	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001640	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0007009	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000405	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002019	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0012185	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000750	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000726	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000734	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000268	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001260	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000943	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002015	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0030195	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001371	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001288	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002159	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001007	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000238	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0006801	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000752	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000710	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:5200321	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002659	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001249	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000256	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000158	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000410	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001270	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002870	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0007759	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000648	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000388	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000580	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002505	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002344	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001538	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0005425	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0004349	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0012664	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0011947	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000546	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000510	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000407	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001328	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000664	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0100874	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0009928	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0012471	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000391	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0031458	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000708	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0410263	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000280	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001133	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0030838	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002254	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0100512	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0000662	ORPHA:581	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0001257	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0011110	ORPHA:581	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002781	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0003541	ORPHA:581	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:581	Mucopolysaccharidosis type 3		HP:0002119	ORPHA:581	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0001249	ORPHA:496790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0001263	ORPHA:496790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0008936	ORPHA:496790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0001257	ORPHA:496790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0002064	ORPHA:496790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0002151	ORPHA:496790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0002465	ORPHA:496790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0003477	ORPHA:496790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0007210	ORPHA:496790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000028	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000276	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000303	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000347	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000348	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000490	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000518	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000545	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000565	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000582	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000609	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000639	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000648	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000768	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0000823	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0001272	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0001385	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0001639	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0002066	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0002360	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0002650	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0003196	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0003535	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0005656	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0011968	ORPHA:496790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0001250	ORPHA:496790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496790	Ocular anomalies-axonal neuropathy-developmental delay syndrome		HP:0007957	ORPHA:496790	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000256	ORPHA:580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000280	ORPHA:580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001376	ORPHA:580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001627	ORPHA:580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0004322	ORPHA:580	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000023	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000158	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000212	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000293	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000405	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000407	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000488	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000546	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000708	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000762	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000943	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001268	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001510	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001537	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001609	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001654	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001744	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002028	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002159	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002240	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002344	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002360	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002376	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002788	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0004582	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0005781	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0006979	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0007994	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0008301	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0010535	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0012471	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0030044	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0030812	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0100543	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0410018	ORPHA:580	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000336	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000362	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000431	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000445	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000648	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000752	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001085	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001263	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001334	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001385	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001633	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001638	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001641	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001679	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001702	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002176	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0002781	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0003552	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0007703	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0007957	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0008843	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0010656	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0012185	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0012478	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0030466	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0031416	ORPHA:580	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000718	ORPHA:580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0000822	ORPHA:580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001129	ORPHA:580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0001250	ORPHA:580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0011675	ORPHA:580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0025160	ORPHA:580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:580	Mucopolysaccharidosis type 2		HP:0100710	ORPHA:580	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000179	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000246	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000280	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000389	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000944	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0001387	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0001508	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0002656	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0002788	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0003521	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0007759	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0008155	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0009928	ORPHA:583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000365	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000470	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000885	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0001744	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0002808	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0002857	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0003300	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0100790	ORPHA:583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000158	ORPHA:583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0000505	ORPHA:583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0001654	ORPHA:583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0030680	ORPHA:583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0030680	ORPHA:583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:583	Mucopolysaccharidosis type 6		HP:0100543	ORPHA:583	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000154	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000164	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000256	ORPHA:582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000280	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000365	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000463	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000470	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000670	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000683	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000768	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000772	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000926	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000944	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0001288	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0001373	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0001654	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0002650	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0002673	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0002750	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0002808	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0002857	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0003416	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0004322	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0004349	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0001382	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0005930	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0006487	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0007957	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0000682	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0003307	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0008155	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0010306	ORPHA:582	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0100543	ORPHA:582	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:582	Mucopolysaccharidosis type 4		HP:0100790	ORPHA:582	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2917	Polydactyly-myopia syndrome		HP:0000545	ORPHA:2917	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2917	Polydactyly-myopia syndrome		HP:0001162	ORPHA:2917	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2917	Polydactyly-myopia syndrome		HP:0000023	ORPHA:2917	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2917	Polydactyly-myopia syndrome		HP:0000028	ORPHA:2917	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2917	Polydactyly-myopia syndrome		HP:0100541	ORPHA:2917	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0000010	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0000246	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0000389	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001367	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001369	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001376	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001482	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001701	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001744	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001824	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001873	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001875	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0001903	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002102	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002205	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002206	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002240	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002665	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002716	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002719	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002721	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002797	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002829	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0002960	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0004332	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0005528	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0006532	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0007400	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0007440	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0009830	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0012384	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0100534	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0100658	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0100769	ORPHA:47612	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0100776	ORPHA:47612	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:47612	Felty syndrome		HP:0100806	ORPHA:47612	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0002251	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0002650	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0002705	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0004736	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0005817	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0006297	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0010441	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0010800	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0011069	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0012738	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0100335	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000161	ORPHA:2919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0001162	ORPHA:2919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0001830	ORPHA:2919	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000191	ORPHA:2919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000288	ORPHA:2919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000316	ORPHA:2919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0001249	ORPHA:2919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0002007	ORPHA:2919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0010297	ORPHA:2919	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000185	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000190	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000193	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000252	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0000668	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0001274	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2919	Orofaciodigital syndrome type 5		HP:0001636	ORPHA:2919	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000175	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000233	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000303	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000322	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000363	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000402	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000405	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000431	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000445	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000677	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000932	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001263	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001320	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001792	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001833	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001852	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0002714	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0004470	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0009882	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0010743	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0011039	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0011220	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0011800	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0012745	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0045025	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0410030	ORPHA:217017	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0000369	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001249	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001627	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0001631	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0004451	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0008551	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0012704	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217017	Zechi-Ceide syndrome		HP:0100874	ORPHA:217017	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0001162	ORPHA:2920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0002187	ORPHA:2920	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000303	ORPHA:2920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0001344	ORPHA:2920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0001830	ORPHA:2920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0001831	ORPHA:2920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0002069	ORPHA:2920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0002465	ORPHA:2920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0010554	ORPHA:2920	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000218	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000252	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000322	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000385	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000387	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000574	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0000689	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0001212	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0001511	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0001812	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0002558	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0002650	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0002987	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0004209	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0006380	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2920	Oliver syndrome		HP:0100490	ORPHA:2920	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0000480	ORPHA:2921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0000567	ORPHA:2921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0001249	ORPHA:2921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0001263	ORPHA:2921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0100258	ORPHA:2921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0000486	ORPHA:2921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0001141	ORPHA:2921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0012109	ORPHA:2921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2921	Preaxial polydactyly-colobomata-intellectual disability syndrome		HP:0030515	ORPHA:2921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000252	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000750	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001249	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001263	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001288	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001999	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0003086	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0011968	ORPHA:464306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000505	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000708	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000729	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000733	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000739	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001250	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001508	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001511	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001518	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002119	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002373	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002465	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0011451	ORPHA:464306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000028	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000341	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000400	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000411	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000426	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000483	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000486	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000490	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000540	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000543	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000545	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000577	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000646	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000752	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001166	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001659	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001770	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002013	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002020	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002079	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002120	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002365	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002719	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002828	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0004209	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0007957	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0010442	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0010627	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0010864	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0011832	ORPHA:464306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000047	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000054	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000107	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000122	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000125	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000126	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000767	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0000964	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001562	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001629	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001643	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001650	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0001822	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002021	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002247	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002280	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002650	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0002808	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0003187	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0003319	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0004322	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464306	DYRK1A-related intellectual disability syndrome		HP:0010219	ORPHA:464306	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002240	ORPHA:2924	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0003270	ORPHA:2924	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0006557	ORPHA:2924	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0005562	ORPHA:2924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0033842	ORPHA:2924	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0000952	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0001654	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0001732	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002020	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002027	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002086	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002093	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002094	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002239	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0002617	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0003155	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0003418	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0003573	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0004944	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0008872	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0010741	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2924	Isolated polycystic liver disease		HP:0030948	ORPHA:2924	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0001460	ORPHA:2926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0003202	ORPHA:2926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0003560	ORPHA:2926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0007328	ORPHA:2926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0040129	ORPHA:2926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0100490	ORPHA:2926	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0000966	ORPHA:2926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0002046	ORPHA:2926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2926	Digital extensor muscle aplasia-polyneuropathy		HP:0004370	ORPHA:2926	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0001260	ORPHA:217012	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0001272	ORPHA:217012	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0002066	ORPHA:217012	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0000639	ORPHA:217012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0001265	ORPHA:217012	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0000365	ORPHA:217012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0001257	ORPHA:217012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0001337	ORPHA:217012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0001347	ORPHA:217012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0002495	ORPHA:217012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:217012	Spinocerebellar ataxia type 31		HP:0006801	ORPHA:217012	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0001647	ORPHA:402075	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0001650	ORPHA:402075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0001659	ORPHA:402075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0001680	ORPHA:402075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0004380	ORPHA:402075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0004962	ORPHA:402075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0030148	ORPHA:402075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0000822	ORPHA:402075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0005113	ORPHA:402075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0004383	ORPHA:402075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0004933	ORPHA:402075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:402075	Familial bicuspid aortic valve		HP:0011103	ORPHA:402075	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001263	ORPHA:314679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001999	ORPHA:314679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0008551	ORPHA:314679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0008872	ORPHA:314679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0008947	ORPHA:314679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0012385	ORPHA:314679	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000089	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000239	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000347	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000405	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000938	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001159	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002342	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002778	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0011471	ORPHA:314679	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000047	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000160	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000252	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000286	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000316	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000327	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000431	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0000581	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001004	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001251	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001274	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001320	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001545	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001627	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001642	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0001762	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002025	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002079	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002119	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002282	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002779	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0002825	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0004322	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0006989	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0008197	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0010864	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0040079	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0100716	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314679	Cerebrofacioarticular syndrome		HP:0200138	ORPHA:314679	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000232	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000252	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000280	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000486	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000488	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000512	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000613	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000639	ORPHA:578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000691	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000708	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0000982	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0001249	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0001251	ORPHA:578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0001252	ORPHA:578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0001288	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0001344	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0001347	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0002353	ORPHA:578	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0002816	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0004345	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0004422	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0005105	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0007281	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0007703	ORPHA:578	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0007957	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0010318	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:578	Mucolipidosis type IV		HP:0011020	ORPHA:578	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0002857	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0003307	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0007957	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0000269	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0000505	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0001387	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0003264	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0003272	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0003312	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0004322	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0004493	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0008818	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0008821	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0025261	ORPHA:577	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0000280	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0000938	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0000943	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0001385	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0001634	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0002650	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0002758	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0009837	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0012185	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0012532	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0030680	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0034337	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0100543	ORPHA:577	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0000885	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0001072	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0001653	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0001659	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0002091	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0002176	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0002515	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0004349	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:577	Mucolipidosis type III		HP:0012378	ORPHA:577	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000175	ORPHA:440354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000347	ORPHA:440354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000774	ORPHA:440354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0002781	ORPHA:440354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0002983	ORPHA:440354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0008905	ORPHA:440354	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000162	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000407	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000520	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000882	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0000947	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0001156	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0001622	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0002007	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0002980	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0003016	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0003097	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0011003	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440354	Autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome		HP:0011800	ORPHA:440354	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000023	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000179	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000212	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000232	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000238	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000246	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000256	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000268	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000271	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000280	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000293	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000294	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000365	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000389	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000407	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000488	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000501	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000505	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000648	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000687	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000691	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0000944	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001171	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001249	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001373	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001387	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001608	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001635	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001639	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001646	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001654	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0001744	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0002024	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0002104	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0002205	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0002230	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0002376	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0002650	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0002829	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0003272	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0003312	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0003401	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0003416	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0004322	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0004374	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0005105	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0005280	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0005930	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0007957	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0008155	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0009928	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0010885	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0012735	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0100261	ORPHA:579	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0100625	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0100765	ORPHA:579	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:579	Mucopolysaccharidosis type 1		HP:0100790	ORPHA:579	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0001548	ORPHA:314662	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0009126	ORPHA:314662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0011276	ORPHA:314662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0012032	ORPHA:314662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0025104	ORPHA:314662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0100578	ORPHA:314662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0100774	ORPHA:314662	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0000034	ORPHA:314662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0002019	ORPHA:314662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0010442	ORPHA:314662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0010816	ORPHA:314662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0012725	ORPHA:314662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0030424	ORPHA:314662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314662	Segmental progressive overgrowth syndrome with fibroadipose hyperplasia		HP:0100559	ORPHA:314662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000230	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000963	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000964	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0001025	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0001053	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0001810	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0006323	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0007400	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0008064	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0008066	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0008391	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0008404	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0010783	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0100585	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0200034	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0200039	ORPHA:2907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000160	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000164	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000217	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000225	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000262	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000929	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000972	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0002745	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0010296	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0100587	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0100669	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0200042	ORPHA:2907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000091	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000211	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000365	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000656	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000772	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000795	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0000924	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0001096	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0002860	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0003272	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0004322	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0001382	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0005916	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0006101	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0006740	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0007759	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0010807	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0011024	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2907	Hereditary acrokeratotic poikiloderma		HP:0100490	ORPHA:2907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000230	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000262	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000509	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000656	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000670	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000682	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000704	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000772	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000929	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000962	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000982	ORPHA:2908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000987	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0000992	ORPHA:2908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001000	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001029	ORPHA:2908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001056	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001371	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001581	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001602	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001741	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0001903	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0002015	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0002037	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0002043	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0002583	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0002860	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0004378	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0006101	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0006323	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0007957	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0008065	ORPHA:2908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0008066	ORPHA:2908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0008388	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0010044	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0010047	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0010783	ORPHA:2908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0012227	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0100490	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0100517	ORPHA:2908	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0100633	ORPHA:2908	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2908	Kindler epidermolysis bullosa		HP:0100825	ORPHA:2908	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000988	ORPHA:2909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001029	ORPHA:2909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0025300	ORPHA:2909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000164	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000653	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000789	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000924	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001518	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0004322	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0004349	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0007556	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0007588	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0008066	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0008070	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0010765	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0045075	ORPHA:2909	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000282	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000670	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000682	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000684	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000685	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000691	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0000938	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001010	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001118	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001592	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001597	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001792	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001871	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002013	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002014	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002164	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002659	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0003022	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0003993	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0006498	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0006501	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0008065	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0008069	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0009778	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0011069	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0031367	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0100585	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0100671	ORPHA:2909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001875	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001903	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001909	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0001915	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002671	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002860	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002861	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0002863	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0003761	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0007418	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0011470	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2909	Rothmund-Thomson syndrome		HP:0200044	ORPHA:2909	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0004912	ORPHA:289176	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0000117	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0000407	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0000684	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0001510	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002652	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002653	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002749	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002812	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002814	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002970	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0003020	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0003109	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0004322	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0004576	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0005096	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0005764	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0006463	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0008732	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0010639	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0011001	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0011036	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0012052	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0100511	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0100559	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0100671	ORPHA:289176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0001363	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002024	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0002982	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0003416	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0030757	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0100036	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0100686	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets		HP:0100781	ORPHA:289176	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets	NOT	HP:0001250	ORPHA:289176	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets	NOT	HP:0001324	ORPHA:289176	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:289176	Autosomal recessive hypophosphatemic rickets	NOT	HP:0003472	ORPHA:289176	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000766	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000767	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000768	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000772	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000773	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000776	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000819	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000912	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000921	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001156	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001161	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001171	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001392	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001631	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001651	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002084	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002162	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002488	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001555	ORPHA:2911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0006709	ORPHA:2911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0007485	ORPHA:2911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0009751	ORPHA:2911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0010311	ORPHA:2911	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000089	ORPHA:2911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0001155	ORPHA:2911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0005255	ORPHA:2911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0006008	ORPHA:2911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0009700	ORPHA:2911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0200055	ORPHA:2911	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000028	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000047	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000070	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000076	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000081	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000252	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000356	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000470	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0000545	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002650	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002808	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002814	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002937	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0002974	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0031095	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0003298	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0003422	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0004050	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0004349	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0006101	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0006501	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0006714	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0007477	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0008678	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0009594	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0009601	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0010579	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0040071	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2911	Poland syndrome		HP:0100013	ORPHA:2911	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001324	ORPHA:2912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0012531	ORPHA:2912	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001284	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001287	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001348	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001945	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002013	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002018	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002039	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002315	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002829	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0003202	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0003326	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0003470	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0003546	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0004302	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0007340	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0009004	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0010547	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0011805	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0012378	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0012486	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0025258	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0025439	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0031469	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0040131	ORPHA:2912	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001283	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001618	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002015	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002374	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002380	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002385	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002483	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002487	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002540	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002590	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002721	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002878	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0003401	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0003484	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0004887	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0006824	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0030196	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0030813	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0031058	ORPHA:2912	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0000713	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0000737	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0000822	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001259	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0001289	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002383	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0002615	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2912	Poliomyelitis		HP:0031274	ORPHA:2912	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0000474	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0001156	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0001162	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0001572	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0002937	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0002948	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0003312	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0008479	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0009738	ORPHA:2916	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0000286	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0000303	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0000668	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0000682	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0001347	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0002162	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0002650	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0002808	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0004209	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0004322	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0009906	ORPHA:2916	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0000175	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0000632	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0001357	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0002999	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0003042	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0005988	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0010935	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0030680	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2916	Postaxial polydactyly-dental and vertebral anomalies syndrome		HP:0100672	ORPHA:2916	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000086	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000202	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000238	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000316	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000347	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000365	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000413	ORPHA:268249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000567	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000568	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000572	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000612	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000625	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0000776	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0001256	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0001274	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0001629	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0001680	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0001789	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0001800	ORPHA:268249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0001829	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0002006	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0002575	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0002779	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0004279	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0008437	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0008551	ORPHA:268249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0009892	ORPHA:268249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268249	Mycophenolate mofetil embryopathy		HP:0011803	ORPHA:268249	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000509	ORPHA:33001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000613	ORPHA:33001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0003550	ORPHA:33001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0009743	ORPHA:33001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0200020	ORPHA:33001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000508	ORPHA:33001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000518	ORPHA:33001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000656	ORPHA:33001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0001324	ORPHA:33001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0002619	ORPHA:33001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000010	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000075	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000093	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000175	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000204	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000465	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0000819	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0001581	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0001643	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0001970	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0004930	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0009745	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0011675	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0030680	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0100244	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33001	Lymphedema-distichiasis syndrome		HP:0100820	ORPHA:33001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000708	ORPHA:466950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001249	ORPHA:466950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001256	ORPHA:466950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001263	ORPHA:466950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001270	ORPHA:466950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001999	ORPHA:466950	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000321	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000486	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000504	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000739	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000750	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001319	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002019	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002086	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002360	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0007018	ORPHA:466950	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000125	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000154	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000219	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000286	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000316	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000337	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000358	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000365	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000395	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000414	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000431	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000455	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000490	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000539	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000572	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000574	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000637	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000664	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000718	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000729	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0000954	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001007	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001156	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001212	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001260	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001344	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001513	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001763	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0001956	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002015	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002020	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002069	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002099	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002119	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002205	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0002793	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0003186	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0004279	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0005280	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0005288	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0008081	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0009794	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0011147	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0011171	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0011220	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0011822	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0012076	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0012704	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0040288	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0100581	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0100702	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466950	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation		HP:0100716	ORPHA:466950	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35664	ALDH18A1-related De Barsy syndrome		HP:0000518	ORPHA:35664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35664	ALDH18A1-related De Barsy syndrome		HP:0000974	ORPHA:35664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35664	ALDH18A1-related De Barsy syndrome		HP:0001249	ORPHA:35664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35664	ALDH18A1-related De Barsy syndrome		HP:0001263	ORPHA:35664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35664	ALDH18A1-related De Barsy syndrome		HP:0001382	ORPHA:35664	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000708	ORPHA:261197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000729	ORPHA:261197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001263	ORPHA:261197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000256	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000750	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001249	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001256	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001270	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001328	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0006863	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0007018	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0009088	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0011351	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0410263	ORPHA:261197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000316	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000337	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000347	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000405	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000407	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000717	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000733	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0012760	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001250	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001266	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001332	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001508	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001513	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001627	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001631	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001646	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001999	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0002020	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0002119	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0002280	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0002650	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0002691	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0003468	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0007099	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0007166	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0011098	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0011800	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0011968	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0100702	ORPHA:261197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000003	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000175	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000776	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0000902	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001161	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001363	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0001651	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0002021	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261197	Proximal 16p11.2 microdeletion syndrome		HP:0003396	ORPHA:261197	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0000582	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0000944	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0001072	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0001156	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0001167	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0001288	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0001387	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0002816	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0003312	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0003510	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0005916	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0005930	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0011304	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0100490	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0100679	ORPHA:2900	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0000581	ORPHA:2900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0001482	ORPHA:2900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0002650	ORPHA:2900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0002967	ORPHA:2900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0012745	ORPHA:2900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0100795	ORPHA:2900	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0000486	ORPHA:2900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2900	Leri pleonosteosis		HP:0003042	ORPHA:2900	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0001271	ORPHA:2901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0002829	ORPHA:2901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0003457	ORPHA:2901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0003484	ORPHA:2901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0009129	ORPHA:2901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0012513	ORPHA:2901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0000912	ORPHA:2901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0003401	ORPHA:2901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0003691	ORPHA:2901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0000160	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0000175	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0000193	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0000286	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0000311	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0001063	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0001159	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0002093	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0002167	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0002360	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0004322	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0005989	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0009830	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0012745	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2901	Neuralgic amyotrophy		HP:0033748	ORPHA:2901	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000023	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000164	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000175	ORPHA:261190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000252	ORPHA:261190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000276	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000307	ORPHA:261190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000319	ORPHA:261190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000322	ORPHA:261190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000341	ORPHA:261190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000343	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000369	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000426	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000444	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000490	ORPHA:261190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000717	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0001061	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0001249	ORPHA:261190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0001250	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0001263	ORPHA:261190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0001601	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0001631	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0002650	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0002721	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0002808	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0004322	ORPHA:261190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0004422	ORPHA:261190	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0000750	ORPHA:261190	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261190	Cleft palate-congenital heart defect-intellectual disability syndrome due to 15q14 microdeletion		HP:0001629	ORPHA:261190	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0031983	ORPHA:2902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0032177	ORPHA:2902	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0001047	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0001974	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0002091	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0002094	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0002099	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0002960	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0003212	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0003565	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0006516	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0011227	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0012418	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0030828	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0030830	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0031246	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0032017	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0032061	ORPHA:2902	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0001824	ORPHA:2902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0001945	ORPHA:2902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0002829	ORPHA:2902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0025406	ORPHA:2902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0030166	ORPHA:2902	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0002202	ORPHA:2902	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0011024	ORPHA:2902	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0011354	ORPHA:2902	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2902	Idiopathic chronic eosinophilic pneumonia		HP:0100750	ORPHA:2902	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2903	Familial spontaneous pneumothorax		HP:0002086	ORPHA:2903	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2903	Familial spontaneous pneumothorax		HP:0002103	ORPHA:2903	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2903	Familial spontaneous pneumothorax		HP:0002107	ORPHA:2903	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001271	ORPHA:2905	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000135	ORPHA:2905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000818	ORPHA:2905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0003271	ORPHA:2905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0005523	ORPHA:2905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0010702	ORPHA:2905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0011122	ORPHA:2905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000771	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000819	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000821	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000953	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000969	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000998	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001028	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001072	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001085	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001284	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001324	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001541	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001698	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001744	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001820	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001824	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001894	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0002092	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0002202	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0002240	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0002694	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0002716	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0003401	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0004054	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0004576	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0004979	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0008207	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0012378	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0012531	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0031052	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0100639	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0100759	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0100925	ORPHA:2905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0000870	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001050	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001063	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0001901	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0002091	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0002747	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0004420	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0004936	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0009125	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0031357	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2905	POEMS syndrome		HP:0100963	ORPHA:2905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002720	ORPHA:420741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002721	ORPHA:420741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0004315	ORPHA:420741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0004322	ORPHA:420741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0006254	ORPHA:420741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0010997	ORPHA:420741	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001328	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001954	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001999	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002090	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0006532	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0011108	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0011109	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0012387	ORPHA:420741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0000252	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0000388	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0000524	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0000712	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001009	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001251	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001263	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001288	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001369	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0001824	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002014	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002027	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002091	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002206	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002312	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002315	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002500	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002850	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0002878	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0004429	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0006530	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0007057	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0007108	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0008940	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0010677	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0010783	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0012768	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0030746	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420741	RIDDLE syndrome		HP:0040189	ORPHA:420741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000708	ORPHA:466943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001249	ORPHA:466943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001263	ORPHA:466943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001999	ORPHA:466943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0008947	ORPHA:466943	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000321	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000356	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000486	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000504	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000739	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000750	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001250	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001344	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002019	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002194	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002360	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002579	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0007018	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0010862	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0011968	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0030190	ORPHA:466943	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000154	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000219	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000286	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000316	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000358	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000395	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000414	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000431	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000455	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000483	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000490	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000545	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000637	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000664	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000718	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000729	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001156	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001260	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001513	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002015	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002020	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002099	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002119	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002342	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002311	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002714	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002719	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0003186	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0005280	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0006889	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0011220	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0011822	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0012704	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0030863	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0040288	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0100704	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0100716	ORPHA:466943	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000125	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000405	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000407	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0000954	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0001763	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002069	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002121	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0002373	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0004279	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0008081	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0100581	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:466943	WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome		HP:0100702	ORPHA:466943	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0001917	ORPHA:314652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0012185	ORPHA:314652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0012622	ORPHA:314652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0000157	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0002176	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0002756	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0003365	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0005244	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0007141	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0010286	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0011805	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0011915	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0012065	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0012280	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0012309	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0012332	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0012664	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0025015	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0030834	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0030836	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0030839	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0030843	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0031368	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314652	Variant ABeta2M amyloidosis		HP:0100292	ORPHA:314652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000218	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000341	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000347	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000506	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000508	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000750	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0001270	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0001319	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0002002	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0002098	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0002353	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0005280	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0005338	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0005487	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0008872	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0010804	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0010864	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0012444	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0012448	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0410263	ORPHA:314655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000369	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000463	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0000494	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0001250	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0001336	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0001627	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0002104	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0002791	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0003196	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0006532	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0006829	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0010442	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0011097	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0011098	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0011167	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0011951	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314655	Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion		HP:0025190	ORPHA:314655	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0001952	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0003074	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0003076	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0004924	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0030794	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0040214	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0040216	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0040217	ORPHA:552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0000112	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0000488	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0000825	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0000831	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0001511	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0001520	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0001998	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0008255	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0025502	ORPHA:552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0000077	ORPHA:552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0000107	ORPHA:552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0000119	ORPHA:552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0001513	ORPHA:552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0001738	ORPHA:552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0002594	ORPHA:552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY		HP:0012028	ORPHA:552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY	NOT	HP:0000956	ORPHA:552	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY	NOT	HP:0001953	ORPHA:552	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:552	MODY	NOT	HP:0030057	ORPHA:552	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0000407	ORPHA:551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0000648	ORPHA:551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0001012	ORPHA:551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0001251	ORPHA:551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0002123	ORPHA:551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0003198	ORPHA:551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0003200	ORPHA:551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0003457	ORPHA:551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0004322	ORPHA:551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0100022	ORPHA:551	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:551	MERRF		HP:0100543	ORPHA:551	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000508	ORPHA:254892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000544	ORPHA:254892	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000338	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000496	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000597	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000602	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002067	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002322	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003198	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003200	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003458	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003546	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003547	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003688	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003690	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003731	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003737	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0010628	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0012103	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0012378	ORPHA:254892	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000365	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000505	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000518	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000716	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000739	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001251	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001254	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001260	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001265	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001272	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001288	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001290	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001337	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001349	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001508	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001644	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001712	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001952	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002015	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002019	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002020	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002063	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002066	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002071	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002093	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002151	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002359	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002375	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002396	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002578	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002875	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003236	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003326	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003388	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003477	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003551	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0004308	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0005110	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0007042	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0009830	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0011675	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0012664	ORPHA:254892	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000017	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000819	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000821	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000836	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000853	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000939	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0000969	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001250	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001276	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001392	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001946	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0001962	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002076	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0002910	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003394	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0003438	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0007302	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0100543	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254892	Autosomal dominant progressive external ophthalmoplegia		HP:0100704	ORPHA:254892	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001249	ORPHA:508498	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000219	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000308	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000343	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000365	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000431	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000470	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000589	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000998	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001155	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002761	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0004322	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0011842	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0011968	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0030680	ORPHA:508498	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000047	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000085	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000089	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000104	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000125	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000252	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000303	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000347	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000480	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000486	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000540	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000545	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000565	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000568	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000609	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000612	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000646	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000729	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000733	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000767	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0000974	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001052	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001177	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001274	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001629	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001636	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001647	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001659	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001660	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001680	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001738	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001763	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0001845	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002079	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002119	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002360	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002414	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002827	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002942	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002943	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0002949	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0003835	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0004209	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0004279	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0004691	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0005620	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0006009	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0006695	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0006712	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0006970	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0007687	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0007874	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0008467	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0009237	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0009997	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0010055	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0010628	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0011304	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0011682	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0012487	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0012745	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0012795	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508498	Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome		HP:0025481	ORPHA:508498	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000726	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001250	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001324	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002076	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002151	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002353	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002381	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002401	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0003128	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0003200	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0008316	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0012429	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0012766	ORPHA:550	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000407	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000572	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000709	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000716	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000736	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000739	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000819	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001251	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001269	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001288	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001298	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001328	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001336	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002013	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002069	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002135	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002331	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002354	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002490	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002922	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0003198	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0004322	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0007159	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0007359	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0009830	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0010794	ORPHA:550	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000093	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000097	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000112	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000114	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000580	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000590	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000648	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000751	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000998	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001045	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001263	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001270	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001274	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001345	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001508	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001638	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001639	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001644	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001716	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001903	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0001945	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002014	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002019	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002079	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002092	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002120	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0002579	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0003477	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0003546	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0004372	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0004389	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0005157	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0005978	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0007067	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0007141	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0007302	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0007327	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0010783	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0011442	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0012444	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0012707	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0025268	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0031546	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0100027	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0100651	ORPHA:550	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000044	ORPHA:550	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000821	ORPHA:550	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:550	MELAS		HP:0000829	ORPHA:550	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001249	ORPHA:268261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001263	ORPHA:268261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001288	ORPHA:268261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001999	ORPHA:268261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0011968	ORPHA:268261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0410263	ORPHA:268261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000119	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000252	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000426	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000478	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001182	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001250	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001251	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001344	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001511	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001518	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001531	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001760	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001780	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002019	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002119	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002136	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002365	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002465	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0003429	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0004322	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0005768	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0011757	ORPHA:268261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000010	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000023	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000028	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000041	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000047	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000049	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000122	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000278	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000411	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000430	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000455	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000486	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000490	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000518	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000540	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000545	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000565	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000582	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000718	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000729	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000739	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000767	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000818	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001276	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001562	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001822	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002015	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002020	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002021	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002033	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002069	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002079	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002120	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002123	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002171	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002360	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002373	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002650	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0002808	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0003196	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0010819	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0010946	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0011147	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0011470	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0011822	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0011917	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0012171	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0025163	ORPHA:268261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000054	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000185	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000365	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000483	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000541	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000612	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000687	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000821	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000824	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0000960	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001256	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001627	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001629	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001641	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001650	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0001659	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0010314	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0010442	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0011069	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0040188	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:268261	DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion		HP:0100783	ORPHA:268261	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000174	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000377	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000708	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000750	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001249	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001263	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001270	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001999	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0002354	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0006891	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0007018	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0010522	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0410263	ORPHA:261183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000252	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000337	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000717	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000729	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0000736	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001250	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001251	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001627	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0002172	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0002311	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0100716	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0100753	ORPHA:261183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001629	ORPHA:261183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001631	ORPHA:261183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001636	ORPHA:261183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0001680	ORPHA:261183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0002198	ORPHA:261183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261183	15q11.2 microdeletion syndrome		HP:0005160	ORPHA:261183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000256	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001250	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001252	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001263	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001355	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001561	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001999	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0012469	ORPHA:500533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0002119	ORPHA:500533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0012430	ORPHA:500533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0030891	ORPHA:500533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000121	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000154	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000194	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000275	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000297	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000348	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0000873	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001344	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001382	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001508	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001631	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0001635	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0002133	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0002307	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0002384	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0002553	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0003199	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0006829	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0010804	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0011182	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0011344	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0011968	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500533	Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome		HP:0030680	ORPHA:500533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0000083	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0000093	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0000738	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0000790	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0000952	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0001251	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0001324	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0001701	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0001733	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0001744	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0001888	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0001945	ORPHA:549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002014	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002017	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002027	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002039	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002076	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002088	ORPHA:549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002091	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002093	ORPHA:549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002103	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002105	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002113	ORPHA:549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002383	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002615	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002716	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002829	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0002902	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0003326	ORPHA:549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0004372	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0005528	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0009830	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0011675	ORPHA:549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0012115	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0012378	ORPHA:549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0012735	ORPHA:549	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0012819	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0100584	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0100658	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0100749	ORPHA:549	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0100776	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:549	Legionnaires disease		HP:0100806	ORPHA:549	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0009830	ORPHA:548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000962	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000966	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0002231	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0003202	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0003401	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0003489	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0006121	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0010829	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0010835	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012181	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012332	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012645	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0020073	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0034102	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0200036	ORPHA:548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000421	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0001026	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0001324	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0001596	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0002087	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0002223	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0003376	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0007460	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0009027	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0010827	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0011334	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0011457	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0011821	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012155	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012185	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012500	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012534	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0012804	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0030003	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0030351	ORPHA:548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000501	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000554	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000618	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000771	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0000834	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0001101	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0001392	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0001743	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0005561	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0032404	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:548	Leprosy		HP:0100583	ORPHA:548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0001824	ORPHA:545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0001945	ORPHA:545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0002665	ORPHA:545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0002716	ORPHA:545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0100721	ORPHA:545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0001744	ORPHA:545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0012378	ORPHA:545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0030166	ORPHA:545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0001004	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0001287	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0002202	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0002585	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0003072	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0025435	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0001541	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0200036	ORPHA:545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:545	Follicular lymphoma		HP:0033823	ORPHA:545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:208999	Paraneoplastic sensory ganglionopathy		HP:5000016	ORPHA:208999	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0001304	ORPHA:99657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0000473	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0000643	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0001260	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0001337	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0001288	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0002451	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0004305	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0011968	ORPHA:99657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99657	Primary dystonia, DYT2 type		HP:0007325	ORPHA:99657	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001873	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001903	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001945	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002910	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002958	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0003073	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0003281	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0011112	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0011118	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0012145	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0012156	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0030356	ORPHA:540	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0000967	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0000979	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0000988	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001019	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001410	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001744	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001875	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002086	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002155	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002240	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002611	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002716	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0003256	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0011121	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0011900	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0012177	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0012211	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0012229	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0030783	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0031364	ORPHA:540	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0000707	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0000952	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0000978	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001250	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0001259	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002383	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002500	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0002583	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0004302	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0004313	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0009830	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0040186	ORPHA:540	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:540	Familial hemophagocytic lymphohistiocytosis		HP:0000407	ORPHA:540	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0002149	ORPHA:543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0005561	ORPHA:543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0025435	ORPHA:543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0100649	ORPHA:543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0000137	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0001392	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0001732	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0001743	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0002017	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0002027	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0002239	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0002733	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0005214	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:543	Burkitt lymphoma		HP:0032218	ORPHA:543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0000182	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0000508	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0000597	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0000640	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0000648	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0000716	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0000739	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0001260	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0001310	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0001332	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0001336	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0001337	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0002066	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0002073	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0002075	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0002076	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0002151	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0002344	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0002448	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0003198	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0003348	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0003390	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0006554	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0007334	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0012377	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0012692	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0025722	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254881	Spinocerebellar ataxia with epilepsy		HP:0033720	ORPHA:254881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007722	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000622	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000505	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0011488	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0011484	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007787	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0001116	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000541	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0012230	ORPHA:364055	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000546	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000662	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000550	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000639	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007695	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0012434	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0002172	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007994	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000613	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000577	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000543	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0012426	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007843	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007703	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0001103	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007814	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007737	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000551	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007663	ORPHA:364055	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000545	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0000533	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0002317	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0011342	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364055	Severe early-childhood-onset retinal dystrophy		HP:0007793	ORPHA:364055	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000298	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000544	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0001638	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002015	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003198	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003200	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003390	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003401	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003688	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003737	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0009830	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0010628	ORPHA:254886	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000365	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000479	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000505	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000508	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000648	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0000716	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0001251	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0001265	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0001272	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0001621	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002059	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002067	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002345	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002362	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002396	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002500	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002548	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002921	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0002936	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003546	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003552	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003701	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0007641	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0025403	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0030237	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0100295	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0100653	ORPHA:254886	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003236	ORPHA:254886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0003691	ORPHA:254886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254886	Autosomal recessive progressive external ophthalmoplegia		HP:0100543	ORPHA:254886	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000028	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000046	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000286	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000316	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000348	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000358	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000378	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0001773	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0002750	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0004209	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0004279	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0006101	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0007598	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0010044	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0010047	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000384	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000413	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000494	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000508	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000520	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000528	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000864	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0001252	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0001263	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0002714	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0004322	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0012521	ORPHA:264200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000248	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000272	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000347	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000430	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000873	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0001274	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0002119	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0010627	ORPHA:264200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000089	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000365	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0000835	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0001558	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:264200	14q22q23 microdeletion syndrome		HP:0001770	ORPHA:264200	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0002448	ORPHA:496756	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0002497	ORPHA:496756	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0003693	ORPHA:496756	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0007269	ORPHA:496756	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0001249	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0001260	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0001263	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0001272	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0001290	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0002079	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0002376	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0003444	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0003477	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0003698	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0009027	ORPHA:496756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0000648	ORPHA:496756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0001285	ORPHA:496756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0002425	ORPHA:496756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0002650	ORPHA:496756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0007199	ORPHA:496756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0012678	ORPHA:496756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome		HP:0001250	ORPHA:496756	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome	NOT	HP:0000829	ORPHA:496756	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:496756	Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome	NOT	HP:0001510	ORPHA:496756	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0000737	ORPHA:500545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0001250	ORPHA:500545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0001263	ORPHA:500545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0001508	ORPHA:500545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0008872	ORPHA:500545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0008947	ORPHA:500545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0012171	ORPHA:500545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0000252	ORPHA:500545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0002187	ORPHA:500545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0002360	ORPHA:500545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0002521	ORPHA:500545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0010864	ORPHA:500545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0000455	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0001118	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0001257	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0001371	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0002059	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0002376	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0002650	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0005949	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0012430	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0012448	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500545	Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract		HP:0040288	ORPHA:500545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0000008	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0000238	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0000648	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0000790	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0001000	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0001004	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0001250	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0001541	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0001945	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002027	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002091	ORPHA:538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002094	ORPHA:538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002097	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002105	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002107	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002113	ORPHA:538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002205	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002239	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0002716	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0005562	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0006772	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0009594	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0009721	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0009726	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0010310	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0011852	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0012086	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0012378	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0012733	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0012735	ORPHA:538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0012798	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0100543	ORPHA:538	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0100749	ORPHA:538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0100750	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0100763	ORPHA:538	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:538	Lymphangioleiomyomatosis		HP:0100804	ORPHA:538	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001824	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001873	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001875	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001959	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002015	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0008066	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0010783	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0012378	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0012733	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0100792	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0100806	ORPHA:537	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001903	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002024	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002027	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002205	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002910	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0003781	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0012735	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0100518	ORPHA:537	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0000083	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0000142	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0000509	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0000572	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0000613	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0000621	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0000795	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001637	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001645	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0001733	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002017	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002091	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002098	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002103	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002239	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0002575	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0006554	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0031368	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0200020	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:537	Toxic epidermal necrolysis		HP:0200042	ORPHA:537	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0000853	ORPHA:319487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0002176	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0002653	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0002730	ORPHA:319487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0002733	ORPHA:319487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0002757	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0002895	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0003003	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0005994	ORPHA:319487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0006528	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0006731	ORPHA:319487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0006766	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0012288	ORPHA:319487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:0012531	ORPHA:319487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319487	Familial papillary or follicular thyroid carcinoma		HP:3000037	ORPHA:319487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000093	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000518	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000615	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000639	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000646	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000716	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000733	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000739	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001249	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001284	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001319	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001608	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001944	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002049	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002150	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002381	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002902	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0003355	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0004322	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100820	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000028	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000276	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000293	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000358	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000411	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000490	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000501	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000557	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000722	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000843	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001250	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001369	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001386	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001508	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001873	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002007	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002019	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000083	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000091	ORPHA:534	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002119	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002169	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002209	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002213	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002353	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002650	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002749	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002757	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002900	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001382	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0007018	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0007513	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0008069	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0008872	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100512	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100530	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100716	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100835	ORPHA:534	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000023	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000027	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000121	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000164	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000189	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000194	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000219	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000230	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000232	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000303	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000343	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000347	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000389	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000486	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000568	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000582	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000632	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000670	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000678	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000679	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000682	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000684	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000704	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000772	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000787	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000790	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000823	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000859	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000873	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000926	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000944	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0000987	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001387	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001522	ORPHA:534	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001537	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0001903	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002002	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002020	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002024	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002093	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002148	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002151	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002205	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002808	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002827	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002857	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0002999	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0003124	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0005469	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0005562	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0005930	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0007731	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0007957	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0009804	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0010471	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0010807	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0011527	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100493	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100589	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100612	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100750	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0100825	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:534	Oculocerebrorenal syndrome of Lowe		HP:0200042	ORPHA:534	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002315	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002922	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0003326	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0010987	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0011450	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0011972	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0012378	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0025143	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0025258	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0031864	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0000236	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0000737	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001250	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001251	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001269	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001336	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001337	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001622	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002014	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002027	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002721	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002829	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002878	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002955	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0003418	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0003474	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0005268	ORPHA:533	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0006824	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0007185	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0012330	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0025615	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0030049	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0031179	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0100022	ORPHA:533	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0000365	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0000509	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0000572	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0000952	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001082	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001249	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001297	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001635	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001701	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001919	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002090	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002098	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002383	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002586	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002754	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0003095	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001945	ORPHA:533	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0001287	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002013	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0002018	ORPHA:533	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0003201	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0004302	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0005521	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0007432	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0011955	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0012089	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0012747	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0012819	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0025059	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0032162	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0100523	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0100584	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0100806	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:533	Listeriosis		HP:0200039	ORPHA:533	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0033726	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0034076	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0034077	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0045042	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:5000038	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0000155	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0000093	ORPHA:536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001824	ORPHA:536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001945	ORPHA:536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0002039	ORPHA:536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0003493	ORPHA:536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0012378	ORPHA:536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0033834	ORPHA:536	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0000790	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0000822	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001369	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001596	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001882	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0003453	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0005421	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0005764	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0012085	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0025300	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0030880	ORPHA:536	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0000716	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0000992	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001250	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001873	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0001878	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0002716	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0007417	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0020151	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0032235	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0033028	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0033040	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0033556	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0034093	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0034096	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0045073	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0100669	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0100755	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0100825	ORPHA:536	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0000488	ORPHA:536	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536	Systemic lupus erythematosus		HP:0002072	ORPHA:536	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0012321	ORPHA:99646	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0003016	ORPHA:99646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0003025	ORPHA:99646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0005701	ORPHA:99646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0005868	ORPHA:99646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0011849	ORPHA:99646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000926	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001367	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001508	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001510	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001511	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0003021	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0003301	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0004322	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0009803	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0030294	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0030295	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0030296	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0030297	ORPHA:99646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000122	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000233	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000256	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000278	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000337	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000343	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000400	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000470	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000494	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000506	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000519	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000666	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000914	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0000958	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001048	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001263	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001270	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001290	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001601	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0001684	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0002033	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0002098	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0002119	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0002453	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0002515	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0002828	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0002970	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0003029	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0003796	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0004242	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0004626	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0004820	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0004948	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0006532	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0006610	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0007033	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0007361	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0007375	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0007486	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0010576	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0011470	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0011681	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0011968	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0012448	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0012762	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0012766	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0025473	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0030866	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0100255	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0100764	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0100806	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99646	Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria		HP:0200035	ORPHA:99646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0003077	ORPHA:391665	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0003124	ORPHA:391665	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0003141	ORPHA:391665	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0004416	ORPHA:391665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0005177	ORPHA:391665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0000822	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001397	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001645	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001658	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001681	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001920	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0002094	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001677	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0004950	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0005162	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0005181	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0006693	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0007201	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0012397	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0030148	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0100261	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:3000062	ORPHA:391665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0000799	ORPHA:391665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0000991	ORPHA:391665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001653	ORPHA:391665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0002829	ORPHA:391665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0004381	ORPHA:391665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0004963	ORPHA:391665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0010874	ORPHA:391665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0001138	ORPHA:391665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0012373	ORPHA:391665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0012638	ORPHA:391665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391665	Homozygous familial hypercholesterolemia		HP:0030882	ORPHA:391665	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001531	ORPHA:574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000218	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000286	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000294	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000308	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000341	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000369	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000494	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001249	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001263	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001511	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001631	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001873	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001903	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0002719	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0005484	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0008897	ORPHA:574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000316	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0000343	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001250	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001273	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0001629	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0002120	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0002623	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0002714	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:574	21q deletion syndrome		HP:0004209	ORPHA:574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0000499	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0000534	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0001597	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0002213	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0002217	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0002232	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0002299	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0007502	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0008070	ORPHA:573	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0000164	ORPHA:573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0000518	ORPHA:573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0001249	ORPHA:573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0100543	ORPHA:573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:573	Monilethrix		HP:0100753	ORPHA:573	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000212	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000280	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001072	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001270	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001537	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001538	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001609	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002474	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0004322	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0006596	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0008897	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0030680	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0031650	ORPHA:576	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000388	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000405	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000774	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001363	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001376	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001633	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001653	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002091	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002465	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002540	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002870	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0005280	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0010444	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0012368	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0045027	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0100543	ORPHA:576	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000023	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000286	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000586	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001433	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001540	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001562	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001638	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001646	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001655	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001659	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001712	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001762	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001824	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002205	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002213	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002808	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0002827	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0003273	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0005487	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0006203	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0006248	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0006380	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0006467	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0007421	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0008936	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0010307	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0011314	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0011359	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0011364	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0012389	ORPHA:576	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0000407	ORPHA:576	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0001744	ORPHA:576	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0004887	ORPHA:576	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:576	Mucolipidosis type II		HP:0011471	ORPHA:576	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000078	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000100	ORPHA:575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000112	ORPHA:575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000174	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000256	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000366	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000408	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000501	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000509	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000554	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000648	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000823	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0000988	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001025	ORPHA:575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001369	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001608	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001744	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001761	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001769	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001903	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001917	ORPHA:575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001939	ORPHA:575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0001945	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0002027	ORPHA:575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0002091	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0002240	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0002633	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0002829	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0003326	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0003565	ORPHA:575	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0004299	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0004322	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0006824	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0008064	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0011107	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0100490	ORPHA:575	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:575	Muckle-Wells syndrome		HP:0100534	ORPHA:575	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0003365	ORPHA:99642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0008800	ORPHA:99642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0008843	ORPHA:99642	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0000924	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0000925	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0000926	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0001288	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0002938	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0003179	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0003273	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0003521	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0004322	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0004594	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0009046	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0010575	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0030043	ORPHA:99642	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0001155	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0001385	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0002515	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0002812	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0002815	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0003510	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0004026	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0005108	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0006387	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0006429	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0008812	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0030839	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99642	Spondyloepimetaphyseal dysplasia, Handigodu type		HP:0100864	ORPHA:99642	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000194	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000298	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000486	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000508	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000602	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0001608	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0006824	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0008872	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0010628	ORPHA:570	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000232	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0001156	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0001252	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0001270	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0001762	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0002015	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0007957	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0009751	ORPHA:570	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000044	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000175	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000218	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000286	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000347	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000365	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000498	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000505	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000691	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0000717	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0001522	ORPHA:570	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0002804	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0003202	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0004050	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0004209	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0004408	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0005914	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0006101	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0006501	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0007565	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0009601	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0009804	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0010295	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0040071	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570	Moebius syndrome		HP:0100783	ORPHA:570	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0031390	ORPHA:572	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002205	ORPHA:572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0004798	ORPHA:572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0005354	ORPHA:572	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0000246	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001508	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002014	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002718	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002726	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002728	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002841	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0004313	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0004385	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0004429	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0005353	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0005368	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0005386	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0005401	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0032218	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0012384	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0025347	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0030991	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0200124	ORPHA:572	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0000371	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0000988	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001875	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001876	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001890	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001904	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001973	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002960	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0003139	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0005403	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0031381	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0031394	ORPHA:572	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001260	ORPHA:572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0001999	ORPHA:572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:572	Immunodeficiency by defective expression of MHC class II		HP:0002066	ORPHA:572	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0003198	ORPHA:254875	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001290	ORPHA:254875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001324	ORPHA:254875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002093	ORPHA:254875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002333	ORPHA:254875	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001252	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001265	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001270	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001531	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002098	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002197	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001288	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002376	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002460	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002747	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002878	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0003202	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0003324	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0003546	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0003698	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0006532	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0007105	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0008872	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0009073	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0012432	ORPHA:254875	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0000590	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0000597	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001260	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001283	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0001488	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002015	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0003326	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0005946	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0008610	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0008625	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0030319	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0100543	ORPHA:254875	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0002650	ORPHA:254875	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254875	Mitochondrial DNA depletion syndrome, myopathic form		HP:0007269	ORPHA:254875	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000627	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000670	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000739	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000829	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000929	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001051	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001061	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001166	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001256	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001263	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001281	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001328	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002019	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002435	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002650	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002901	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0003326	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0004322	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0011840	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0007018	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0011496	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0012732	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0100765	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000023	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000028	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000047	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000076	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000113	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000130	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000160	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000238	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000252	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000262	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000316	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000322	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000347	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000453	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000486	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000494	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000501	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000518	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000568	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000648	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000682	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000708	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000716	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000717	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000765	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000821	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000836	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000979	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001053	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001081	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001136	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001161	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001249	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001250	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001300	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001369	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001508	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001511	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001513	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001537	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001561	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001601	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001643	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001646	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001744	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001762	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001829	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001872	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001873	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002020	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002023	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002099	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002101	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002139	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002239	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002251	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002414	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002566	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002607	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002619	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002960	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002999	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0005562	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001382	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0006510	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0007302	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0008872	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0011324	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0011662	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0100735	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0100750	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0100753	ORPHA:567	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000175	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000286	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000369	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000405	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000414	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000426	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000431	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000506	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000582	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000600	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000778	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001252	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001611	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001629	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001631	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001636	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001641	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001660	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0001999	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002381	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002691	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0002721	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0012303	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0030680	ORPHA:567	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000089	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000164	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000272	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000276	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000343	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000365	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000385	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000389	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000396	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000470	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000492	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567	22q11.2 deletion syndrome		HP:0000508	ORPHA:567	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0007695	ORPHA:566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0007730	ORPHA:566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0007990	ORPHA:566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0012805	ORPHA:566	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000483	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000505	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000613	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0007906	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0012047	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0012108	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0031730	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0100018	ORPHA:566	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000485	ORPHA:566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000519	ORPHA:566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000618	ORPHA:566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000622	ORPHA:566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0000662	ORPHA:566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566	Congenital microcoria		HP:0012040	ORPHA:566	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0032900	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0032901	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0200149	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0000360	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001259	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001272	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002301	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002381	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002463	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0007209	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0007979	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0008959	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0010544	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0010829	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0010833	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0011199	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0012044	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0031179	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0032044	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0032506	ORPHA:569	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001249	ORPHA:569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002133	ORPHA:569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0003392	ORPHA:569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0011196	ORPHA:569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0100576	ORPHA:569	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001324	ORPHA:569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002077	ORPHA:569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002167	ORPHA:569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002353	ORPHA:569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0011153	ORPHA:569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0011157	ORPHA:569	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0000365	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0000575	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0000651	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001260	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001269	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001289	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0001308	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002172	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002181	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002321	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0002922	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0003401	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0004305	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0007240	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0010835	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0011172	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0011468	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0012229	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0012508	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:569	Familial or sporadic hemiplegic migraine		HP:0030786	ORPHA:569	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000568	ORPHA:568	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000028	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000047	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000072	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000126	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000164	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000202	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000252	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000358	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000482	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000501	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000567	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000588	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000612	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0001249	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0004209	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0004322	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0006101	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0006482	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000377	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0008678	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0009943	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0100490	ORPHA:568	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000365	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000384	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000465	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000505	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000518	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000639	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000684	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0000889	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0001250	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0002167	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0002650	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0002808	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0003043	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0003307	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0007370	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0009755	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0030680	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0100716	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568	Microphthalmia, Lenz type		HP:0100818	ORPHA:568	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0000822	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001635	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001644	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001649	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001712	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001962	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002094	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002875	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0005135	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0010741	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0011703	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0012378	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0012664	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0012764	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0025169	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0030848	ORPHA:563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001653	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001708	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001907	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002092	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0004756	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0005120	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0005133	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0006705	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0012398	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0012763	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0012819	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0030148	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0030356	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0030830	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0031295	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0100602	ORPHA:563	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0100603	ORPHA:563	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0100749	ORPHA:563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0000819	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001513	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0001903	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002027	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002099	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002401	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002878	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002926	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0002960	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0011713	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:563	Peripartum cardiomyopathy		HP:0030149	ORPHA:563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0010511	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0010529	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0010609	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0010733	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0011067	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0011220	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0011332	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0011406	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0011755	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0012304	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0012584	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0100033	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0100807	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:3000038	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001263	ORPHA:508488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002342	ORPHA:508488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0004322	ORPHA:508488	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000219	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000286	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000293	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000319	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000321	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000343	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000358	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000431	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000455	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000463	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000470	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000729	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001155	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001382	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001511	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001627	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002474	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0004209	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0004220	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0007663	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0008081	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0008872	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0010722	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0011470	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0040019	ORPHA:508488	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000023	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000076	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000077	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000122	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000125	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000300	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000308	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000341	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000480	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000486	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000490	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000527	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000574	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000577	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000582	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000609	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000744	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000752	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000767	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000774	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000817	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000891	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0000954	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001250	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001290	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001374	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001385	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001518	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001562	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001629	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001643	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001660	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001674	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001680	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001738	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001763	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001838	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0001883	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002015	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002020	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002079	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002098	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002101	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002239	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002283	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002553	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002943	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0002983	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0003097	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0003298	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0005176	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0005306	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0005484	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0006695	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0007633	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0009237	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0009796	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0010109	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508488	8q24.3 microdeletion syndrome		HP:0010289	ORPHA:508488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000138	ORPHA:562	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000826	ORPHA:562	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0005605	ORPHA:562	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0031072	ORPHA:562	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000035	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000053	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000124	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000820	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000836	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0001507	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002650	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002693	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002823	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0005616	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0010734	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0010736	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0011821	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0030088	ORPHA:562	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000117	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000144	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000271	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000324	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000365	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000689	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000845	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000853	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000858	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000870	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0001733	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0001742	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002020	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002653	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002749	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002757	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0003401	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0006719	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0008768	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0010735	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0010791	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0012028	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0020110	ORPHA:562	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0000572	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0001396	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0001579	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0001876	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0002148	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0003002	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0003109	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0003118	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0005528	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0012063	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0012115	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:562	McCune-Albright syndrome		HP:0030428	ORPHA:562	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000015	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000023	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000174	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000252	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000269	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000293	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000298	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000347	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000708	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000767	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000774	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000934	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000939	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000944	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000958	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000974	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0000987	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001072	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001249	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001250	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001252	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001257	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001276	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001324	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001511	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001537	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001943	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002017	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002024	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002045	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002072	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002170	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002224	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002239	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002376	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002617	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002645	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002754	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0002757	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0005293	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0005344	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0005599	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0001382	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0006487	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0006579	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0007420	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0008070	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0008368	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0008872	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0010318	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0012378	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0100545	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0100777	ORPHA:565	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0100790	ORPHA:565	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565	Menkes disease		HP:0100806	ORPHA:565	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000003	ORPHA:564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000252	ORPHA:564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001162	ORPHA:564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001830	ORPHA:564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0002084	ORPHA:564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0002612	ORPHA:564	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000028	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000062	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000175	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000293	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000316	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000340	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000347	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000358	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000457	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000482	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000518	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000532	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000568	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000647	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000648	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001562	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001883	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0006870	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0008053	ORPHA:564	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000037	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000068	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000073	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000221	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000238	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0000528	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001177	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001305	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001696	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001737	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001746	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0001747	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0002323	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0006487	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0006706	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0007370	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0010295	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0010459	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0030680	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:564	Meckel syndrome		HP:0100732	ORPHA:564	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000278	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000463	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000520	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000963	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0001249	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0001508	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0003100	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0005616	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0001382	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0006487	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0011220	ORPHA:561	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000194	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000316	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000405	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000592	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000978	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0002230	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0002650	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0002659	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0003196	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0004349	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0010808	ORPHA:561	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000212	ORPHA:561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000453	ORPHA:561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0000648	ORPHA:561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0001321	ORPHA:561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0001363	ORPHA:561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0002119	ORPHA:561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:561	Marshall-Smith syndrome		HP:0030680	ORPHA:561	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000164	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000179	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000215	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000248	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000272	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000316	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000343	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000347	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000407	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000431	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000463	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000518	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000545	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0002829	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0003196	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0004322	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0005280	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0010669	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0012368	ORPHA:560	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000175	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000327	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000501	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000505	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000520	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000541	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000646	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000966	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0001083	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0002514	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0002684	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0002738	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0002758	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0002857	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0004327	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0007773	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0008070	ORPHA:560	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000218	ORPHA:560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000486	ORPHA:560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000639	ORPHA:560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0000653	ORPHA:560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0002007	ORPHA:560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:560	Marshall syndrome		HP:0045075	ORPHA:560	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001622	ORPHA:391673	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0000961	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001518	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001875	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001974	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0002014	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0002902	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0003270	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0004396	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0012378	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0012537	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0025085	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0030144	ORPHA:391673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0000969	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001254	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001541	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001543	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001627	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001662	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001873	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001941	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0001942	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0002013	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0002104	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0002151	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0002586	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0002615	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0003074	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0005521	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0005968	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0011014	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0031273	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0032545	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391673	Necrotizing enterocolitis		HP:0040187	ORPHA:391673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000256	ORPHA:589821	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000297	ORPHA:589821	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0010804	ORPHA:589821	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0031843	ORPHA:589821	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000736	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001319	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001622	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001883	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002119	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002486	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002643	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002650	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0007010	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0011098	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0011705	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0011710	ORPHA:589821	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000518	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000729	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000750	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000752	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0000805	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001558	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001561	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001643	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001671	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002014	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002015	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002019	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002020	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002027	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0002360	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0004325	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0040183	ORPHA:589821	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589821	Congenital-onset Steinert myotonic dystrophy		HP:0001513	ORPHA:589821	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0001290	ORPHA:254864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0001324	ORPHA:254864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0003198	ORPHA:254864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0003200	ORPHA:254864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0003688	ORPHA:254864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0009051	ORPHA:254864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0009058	ORPHA:254864	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0001265	ORPHA:254864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0002098	ORPHA:254864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0004900	ORPHA:254864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0008180	ORPHA:254864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0011923	ORPHA:254864	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0000158	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0000218	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0000707	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0001392	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0001626	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0002033	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0002240	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0003234	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0004887	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0005946	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0011470	ORPHA:254864	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254864	Mitochondrial myopathy with reversible cytochrome C oxidase deficiency		HP:0002194	ORPHA:254864	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000077	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000248	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000252	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000303	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000321	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000322	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000400	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000431	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000541	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000545	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000557	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000558	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000696	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000787	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0000851	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0001182	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0001848	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0002076	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0005487	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0005990	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0008007	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0008619	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0010490	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0010804	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0012448	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0020038	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521445	Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome		HP:0100807	ORPHA:521445	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0009145	ORPHA:42775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000501	ORPHA:42775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000568	ORPHA:42775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000609	ORPHA:42775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001305	ORPHA:42775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001627	ORPHA:42775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001671	ORPHA:42775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0002408	ORPHA:42775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000252	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000315	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000486	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000508	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000518	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000612	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000646	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000647	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000766	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0000821	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001100	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001250	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001252	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001263	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001274	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001321	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001636	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0001680	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0002616	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0004374	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0005306	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0005344	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0007797	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0100028	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0100719	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42775	PHACE syndrome		HP:0100761	ORPHA:42775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0000135	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0000486	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0000518	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001249	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001251	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001252	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001260	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001263	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001321	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001328	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001460	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001618	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0002167	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0002334	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0003198	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0003241	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0003510	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0012400	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0040081	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0045040	ORPHA:559	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0000639	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0000768	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001156	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001167	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001257	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001276	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001385	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0002063	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0002650	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0002673	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0002827	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0003202	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0003552	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0003560	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0004279	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0005743	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0005916	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0010508	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0010547	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0100660	ORPHA:559	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0000252	ORPHA:559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0000648	ORPHA:559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001265	ORPHA:559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0001284	ORPHA:559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:559	Marinesco-Sjögren syndrome		HP:0009830	ORPHA:559	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000012	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000019	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000093	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000140	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000157	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000464	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000790	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000988	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0000989	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0001482	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0001892	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0001945	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0002014	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0002027	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0002721	ORPHA:556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0002729	ORPHA:556	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0011123	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0012735	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0100273	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0100518	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0100577	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0100743	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0100749	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0100787	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0100796	ORPHA:556	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0200034	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556	Malakoplakia		HP:0200042	ORPHA:556	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000232	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000470	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000687	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001249	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001252	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001763	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0006191	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0007552	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0012811	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0045025	ORPHA:487825	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000233	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000248	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000289	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000316	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000319	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000348	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000358	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000365	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000486	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000490	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000506	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001212	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001518	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001831	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0002650	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0006610	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0007367	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0007605	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0009381	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0009909	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0011341	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0011451	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0100872	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0410263	ORPHA:487825	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000028	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000219	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000272	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000400	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000482	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0000568	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001344	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0001382	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0002119	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0002308	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0002536	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0009890	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0011344	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487825	Pierpont syndrome		HP:0012043	ORPHA:487825	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001519	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001533	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001763	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002108	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002616	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0004942	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0012432	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000275	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000505	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000545	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000678	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000767	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001083	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001132	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001382	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001634	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001653	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001659	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001704	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002360	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002647	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002650	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002705	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0003179	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0004970	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0005059	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0007800	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0010535	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0010668	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0012019	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0100775	ORPHA:558	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000023	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000175	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000268	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000278	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000347	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000494	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000501	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000541	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000938	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000939	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001252	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001635	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002097	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002105	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002435	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002636	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002808	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0002996	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0003202	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0003302	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0003326	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0004326	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0004349	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0004382	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0004756	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0004927	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0005162	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0005294	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0006687	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0007018	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0007676	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0007720	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0010807	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0100785	ORPHA:558	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0000768	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001065	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:558	Marfan syndrome		HP:0001166	ORPHA:558	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0000083	ORPHA:510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0000708	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0000790	ORPHA:510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0001256	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0001257	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0001903	ORPHA:510	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0001997	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0002149	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0002342	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0004374	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:510	Lesch-Nyhan syndrome		HP:0100022	ORPHA:510	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000252	ORPHA:391641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0001770	ORPHA:391641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0002589	ORPHA:391641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0005819	ORPHA:391641	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000347	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0001328	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0001999	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0002032	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0004209	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0004220	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0004691	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0004692	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0009577	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0009778	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0012745	ORPHA:391641	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000076	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000077	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000083	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000085	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000110	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000123	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000126	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000405	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0000407	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0001627	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0001643	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0002247	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0010446	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0011611	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0011625	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0011662	ORPHA:391641	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0001249	ORPHA:391641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0002023	ORPHA:391641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0004322	ORPHA:391641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:391641	Feingold syndrome type 1		HP:0005235	ORPHA:391641	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001433	ORPHA:309252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001250	ORPHA:309252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001873	ORPHA:309252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:6000611	ORPHA:309252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:6001185	ORPHA:309252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0000252	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0000365	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0000545	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0000602	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0000938	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001251	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001252	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001336	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001337	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001751	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0001903	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0002353	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency		HP:0002808	ORPHA:309252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309252	Atypical Gaucher disease due to saposin C deficiency	NOT	HP:0003656	ORPHA:309252	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000174	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000239	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000248	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000324	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000347	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000592	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000772	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000774	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0000912	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0001024	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0001252	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0001373	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0002007	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0002644	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0002645	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0003103	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0004322	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0004331	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0005280	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0001382	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0006487	ORPHA:2097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0010807	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0011912	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0012368	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2097	Grant syndrome		HP:0100729	ORPHA:2097	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003546	ORPHA:254854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003551	ORPHA:254854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003701	ORPHA:254854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0009046	ORPHA:254854	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0002359	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0002460	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0002515	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0002600	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003391	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003547	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003722	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003749	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0007126	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0009020	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0030199	ORPHA:254854	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0000590	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0001260	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0001488	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0002505	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0002938	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003326	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003327	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003394	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003731	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0030192	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0030195	ORPHA:254854	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0000651	ORPHA:254854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0001252	ORPHA:254854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0001270	ORPHA:254854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0002650	ORPHA:254854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003201	ORPHA:254854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003652	ORPHA:254854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254854	Pure mitochondrial myopathy		HP:0003691	ORPHA:254854	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000164	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000248	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000294	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000316	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000405	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000478	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000492	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000504	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000639	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000677	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0001760	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0002208	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0002230	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0004322	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0004440	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0005916	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0008497	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0009882	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0009891	ORPHA:2095	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000327	ORPHA:2095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000483	ORPHA:2095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000647	ORPHA:2095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000929	ORPHA:2095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0001537	ORPHA:2095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0001643	ORPHA:2095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0010940	ORPHA:2095	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0000636	ORPHA:2095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2095	Gorlin-Chaudhry-Moss syndrome		HP:0001256	ORPHA:2095	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000158	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000232	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000252	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000286	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000303	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000319	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000411	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000414	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000494	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000581	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0000733	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0001250	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0001252	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0001274	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0001344	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0001510	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0002020	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0002376	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0002650	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0002808	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0003196	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0003781	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0005280	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0005487	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0009738	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0010804	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0010864	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0011968	ORPHA:261144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261144	FOXG1 syndrome due to 14q12 microdeletion		HP:0100540	ORPHA:261144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0000020	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0000648	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0000762	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001250	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001260	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001265	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001290	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001324	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001332	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0002066	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0002312	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0002359	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0002376	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0002415	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0002922	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0003444	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0007133	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0007240	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0030051	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0030081	ORPHA:309256	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0000649	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0000712	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0000738	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0000746	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001082	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001257	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0001939	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0002371	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0003270	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0003487	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0007663	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0008619	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0008872	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0012433	ORPHA:309256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0025013	ORPHA:309256	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:309256	Metachromatic leukodystrophy, late infantile form		HP:0031358	ORPHA:309256	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0200063	ORPHA:157798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0005227	ORPHA:157798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0100808	ORPHA:157798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0100834	ORPHA:157798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0002861	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0002862	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0003002	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0006725	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0012125	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0012189	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0100008	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0100574	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0100615	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157798	Serrated polyposis syndrome		HP:0100728	ORPHA:157798	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000750	ORPHA:364028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001263	ORPHA:364028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000708	ORPHA:364028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001250	ORPHA:364028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001328	ORPHA:364028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001533	ORPHA:364028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002342	ORPHA:364028	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000028	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000054	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000126	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000188	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000189	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000194	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000248	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000256	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000272	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000297	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000303	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000322	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000336	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000400	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000490	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000508	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000675	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000718	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000729	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000742	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0000817	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001256	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001257	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001265	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001270	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001320	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001336	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001382	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0001763	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002069	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002079	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002133	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002360	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002460	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002650	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002719	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002808	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0002816	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0003487	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0004322	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0006863	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0006951	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0006979	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0007021	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0007655	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0008936	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0009909	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0010864	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0012471	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		HP:0030236	ORPHA:364028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000003	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000023	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000085	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000126	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000164	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000307	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000324	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000365	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000369	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000370	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000446	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000486	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000567	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000568	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000612	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000682	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000773	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000776	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000894	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0000963	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001000	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001018	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001083	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001161	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001171	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001482	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001537	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001539	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001540	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001596	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001597	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001629	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001643	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001671	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001770	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0001839	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0002020	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0002027	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0002247	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0002414	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0002650	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0004334	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0004930	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0005930	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0006101	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0006482	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0006554	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0006703	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0007676	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0007957	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0008065	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0008678	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0008839	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0009124	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0009804	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0010783	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0010807	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0011847	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0012733	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0012740	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0045026	ORPHA:2092	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0100490	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0100543	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0100559	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0100560	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0100585	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0100670	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0100790	ORPHA:2092	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2092	Focal dermal hypoplasia		HP:0200036	ORPHA:2092	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0000083	ORPHA:254857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0000590	ORPHA:254857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0001638	ORPHA:254857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0004900	ORPHA:254857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0011344	ORPHA:254857	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0001250	ORPHA:254857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0001254	ORPHA:254857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0001284	ORPHA:254857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0002643	ORPHA:254857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0006583	ORPHA:254857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254857	Lethal infantile mitochondrial myopathy		HP:0008935	ORPHA:254857	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2091	Multinodular goiter-cystic kidney-polydactyly syndrome		HP:0000003	ORPHA:2091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2091	Multinodular goiter-cystic kidney-polydactyly syndrome		HP:0001162	ORPHA:2091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2091	Multinodular goiter-cystic kidney-polydactyly syndrome		HP:0001199	ORPHA:2091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2091	Multinodular goiter-cystic kidney-polydactyly syndrome		HP:0001841	ORPHA:2091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2091	Multinodular goiter-cystic kidney-polydactyly syndrome		HP:0005987	ORPHA:2091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0000252	ORPHA:2090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0000286	ORPHA:2090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0000369	ORPHA:2090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0000494	ORPHA:2090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0000558	ORPHA:2090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0001249	ORPHA:2090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0001622	ORPHA:2090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0002093	ORPHA:2090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0004322	ORPHA:2090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0004467	ORPHA:2090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0005180	ORPHA:2090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0005280	ORPHA:2090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2090	GMS syndrome		HP:0008872	ORPHA:2090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0001892	ORPHA:157794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0002573	ORPHA:157794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0012183	ORPHA:157794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0003003	ORPHA:157794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0005227	ORPHA:157794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0005505	ORPHA:157794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0007378	ORPHA:157794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0012198	ORPHA:157794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0100896	ORPHA:157794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0200063	ORPHA:157794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0002576	ORPHA:157794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0040276	ORPHA:157794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0100743	ORPHA:157794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0002890	ORPHA:157794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0006771	ORPHA:157794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0012114	ORPHA:157794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0012125	ORPHA:157794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:157794	Hereditary mixed polyposis syndrome		HP:0100245	ORPHA:157794	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0001873	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0001945	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002017	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002027	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002039	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002152	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002315	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002615	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002829	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0003326	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0008150	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0030953	ORPHA:509	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0000952	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0000988	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0001287	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0001919	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002011	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002014	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002098	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002105	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002202	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002240	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0002716	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0011705	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0012115	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0012735	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0025143	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0025439	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0031197	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0040223	ORPHA:509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0000554	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0000573	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0001085	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0001701	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0003201	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0011675	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0011896	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0012424	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0030497	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:509	Leptospirosis		HP:0100653	ORPHA:509	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000855	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000962	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000998	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0003162	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0003758	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0008846	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0008897	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0011998	ORPHA:508	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000040	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000065	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000105	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000842	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000956	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0001249	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0001508	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0001639	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0002219	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0002240	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0003202	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0003247	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0003270	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0004325	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0004405	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0004914	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0008665	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0011344	ORPHA:508	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000121	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000252	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000307	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000316	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000369	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000411	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000445	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000848	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000859	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0000974	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0001072	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0001176	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0001833	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0002035	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0002150	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0002900	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0008936	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0011787	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0012471	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0025024	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:508	Donohue syndrome		HP:0100879	ORPHA:508	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0001156	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0001162	ORPHA:2098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0001387	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0001522	ORPHA:2098	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0001773	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0001831	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0002652	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0002983	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0003038	ORPHA:2098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0005048	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0005736	ORPHA:2098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0005914	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0006487	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0008368	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0008873	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0009601	ORPHA:2098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0100242	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2098	Acromesomelic dysplasia, Grebe type		HP:0100387	ORPHA:2098	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505	Graham Little-Piccardi-Lassueur syndrome		HP:0000989	ORPHA:505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505	Graham Little-Piccardi-Lassueur syndrome		HP:0001596	ORPHA:505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505	Graham Little-Piccardi-Lassueur syndrome		HP:0002209	ORPHA:505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505	Graham Little-Piccardi-Lassueur syndrome		HP:0002215	ORPHA:505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505	Graham Little-Piccardi-Lassueur syndrome		HP:0002225	ORPHA:505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505	Graham Little-Piccardi-Lassueur syndrome		HP:0007468	ORPHA:505	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505	Graham Little-Piccardi-Lassueur syndrome		HP:0100725	ORPHA:505	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0000163	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001744	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001876	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001892	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001954	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0002240	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0002716	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0004311	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0011830	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0012384	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0030166	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0200034	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0200035	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0200042	ORPHA:507	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0000980	ORPHA:507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001824	ORPHA:507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001903	ORPHA:507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0002829	ORPHA:507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0002910	ORPHA:507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0003073	ORPHA:507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0010702	ORPHA:507	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001873	ORPHA:507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0001882	ORPHA:507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0002039	ORPHA:507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:507	Leishmaniasis		HP:0012378	ORPHA:507	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0001321	ORPHA:314603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0001347	ORPHA:314603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0002497	ORPHA:314603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0000012	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0000666	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0001256	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0001257	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0001310	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0001332	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0002066	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0002073	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0002120	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0002352	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0002464	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0002650	ORPHA:314603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy		HP:0008619	ORPHA:314603	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002151	ORPHA:506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002490	ORPHA:506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003128	ORPHA:506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003648	ORPHA:506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0008947	ORPHA:506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012379	ORPHA:506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0100022	ORPHA:506	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000407	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000587	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000602	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000648	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000998	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001263	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001508	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001510	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001639	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002171	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002344	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002376	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002415	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002493	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002928	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0004305	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0006943	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0007183	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0008336	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0008972	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0011923	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0011968	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012696	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012707	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012747	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012748	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012751	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0031691	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0100321	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0410263	ORPHA:506	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000508	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000639	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000924	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001250	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001251	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001257	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001264	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001266	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001274	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001324	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001332	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001399	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001635	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001903	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001943	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001993	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002015	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002071	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002072	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002079	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002305	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002460	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002487	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002521	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002542	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002793	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002828	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002878	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002909	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003198	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003202	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003219	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003348	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003390	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0003535	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0008347	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0009830	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0011924	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012120	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0200147	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0410145	ORPHA:506	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000100	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000124	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000348	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000400	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000518	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0000964	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001272	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001511	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001596	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001629	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001875	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001947	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0001999	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002133	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0002579	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0008314	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0011335	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0012469	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0040197	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:506	Leigh syndrome		HP:0100660	ORPHA:506	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0100318	ORPHA:501	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001250	ORPHA:501	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0000712	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0000716	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0000726	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001251	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001257	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001260	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001268	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001288	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001289	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001312	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002100	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002123	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002133	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002315	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002367	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002521	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002540	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0025357	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0040288	ORPHA:501	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001336	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0001399	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002069	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002121	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002360	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0002384	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0007270	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0007334	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0007359	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0007537	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0010819	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0011165	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0012444	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:501	Lafora disease		HP:0031358	ORPHA:501	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000078	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000316	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000407	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000974	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000995	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001003	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001480	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001510	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001511	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001639	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001641	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001642	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0004414	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0008625	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0011675	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0011710	ORPHA:500	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000028	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000144	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000271	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000358	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000431	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000465	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000508	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000767	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000768	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000912	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001633	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001634	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0003691	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0004322	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0006695	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0030680	ORPHA:500	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000047	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000248	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0000325	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001256	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001263	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001482	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001608	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0001658	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0002617	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0002650	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0002861	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0002863	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0003006	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0003298	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0004306	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0007392	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0010318	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:500	Noonan syndrome with multiple lentigines		HP:0100542	ORPHA:500	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0000028	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0000175	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0000272	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0000316	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0000405	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0001156	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0001249	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0001363	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0001626	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0001799	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0002093	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0002650	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0003319	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0003422	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0004232	ORPHA:503	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0004322	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0005008	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0005280	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0001382	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0005930	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0006101	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0008755	ORPHA:503	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0009836	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0009882	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0011220	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0011304	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:503	Larsen syndrome		HP:0012368	ORPHA:503	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000219	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000343	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000358	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000411	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000414	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0002002	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0002209	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0002653	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0002750	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0004322	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0005039	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0010230	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0100777	ORPHA:502	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000574	ORPHA:502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001249	ORPHA:502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001373	ORPHA:502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001582	ORPHA:502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001382	ORPHA:502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0009118	ORPHA:502	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000010	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000076	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000164	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000174	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000252	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000405	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0000431	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001156	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001252	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001385	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001510	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0001883	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0002119	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0002857	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0005743	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0007598	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0009928	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0011069	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:502	Trichorhinophalangeal syndrome type 2		HP:0030680	ORPHA:502	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000315	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000620	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0001733	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0001880	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0002716	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0003212	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0003493	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0007734	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0010824	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0011227	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0011482	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0012393	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0031281	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0032300	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0100539	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:3000061	ORPHA:449563	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000077	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000246	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000492	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000496	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000587	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0002088	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0005200	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0008049	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0009831	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0030669	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0100540	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:3000030	ORPHA:449563	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000024	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000491	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0000579	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0002665	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0003003	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0011747	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0012539	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0030151	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0031912	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0100526	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0100646	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0100661	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0100796	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:449563	IgG4-related ophthalmic disease		HP:0430022	ORPHA:449563	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000572	ORPHA:2086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000639	ORPHA:2086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000648	ORPHA:2086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0001067	ORPHA:2086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0007663	ORPHA:2086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000238	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000486	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000520	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000602	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000618	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000707	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0000826	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0001085	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0001123	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0001250	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0001263	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0001510	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0002013	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0002018	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0002315	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0002321	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0002376	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2086	Optic pathway glioma		HP:0003473	ORPHA:2086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2085	Glaucoma-sleep apnea syndrome		HP:0000501	ORPHA:2085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2085	Glaucoma-sleep apnea syndrome		HP:0002093	ORPHA:2085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2085	Glaucoma-sleep apnea syndrome		HP:0010535	ORPHA:2085	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0001249	ORPHA:565899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0001270	ORPHA:565899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0002465	ORPHA:565899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0003236	ORPHA:565899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0008981	ORPHA:565899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0008994	ORPHA:565899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0100614	ORPHA:565899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0003202	ORPHA:565899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0003698	ORPHA:565899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0005912	ORPHA:565899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0007018	ORPHA:565899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0009046	ORPHA:565899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565899	POMGNT2-related limb-girdle muscular dystrophy R24		HP:0011892	ORPHA:565899	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2084	Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome		HP:0000501	ORPHA:2084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2084	Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome		HP:0001083	ORPHA:2084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2084	Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome		HP:0004322	ORPHA:2084	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0001332	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0001347	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002059	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002180	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002267	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002376	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002478	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0004322	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0007256	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0008936	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0010780	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0100543	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0100852	ORPHA:309246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0000719	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0000739	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0001250	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002072	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002371	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002476	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0008897	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0010729	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0012547	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0030904	ORPHA:309246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0002200	ORPHA:309246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:309246	GM2 gangliosidosis, AB variant		HP:0030081	ORPHA:309246	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000028	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000046	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000126	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000252	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000268	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000347	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000358	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000396	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000400	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000426	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000430	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000470	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0000474	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0001156	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0001250	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0001263	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0001276	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0001510	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0001511	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0001608	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0002057	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0002119	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0002553	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0003196	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0006610	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0007598	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0008736	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0010720	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0012745	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0100490	ORPHA:2083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2083	Prominent glabella-microcephaly-hypogenitalism syndrome		HP:0100543	ORPHA:2083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002119	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002267	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002352	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002478	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002509	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002521	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002536	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002808	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0003196	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0005781	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0007514	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0008278	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0010804	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0011968	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0012098	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0012448	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0012762	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0031162	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0100807	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000407	ORPHA:521426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000639	ORPHA:521426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000975	ORPHA:521426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001250	ORPHA:521426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002483	ORPHA:521426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000218	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000252	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000319	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000343	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000347	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000358	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000648	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000750	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000768	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0000954	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001007	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001162	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001187	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001249	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001252	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001263	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001283	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001332	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001508	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001830	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001838	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0001999	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002063	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002071	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002079	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002093	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521426	PLAA-associated neurodevelopmental disorder		HP:0002104	ORPHA:521426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0000737	ORPHA:2089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0001946	ORPHA:2089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0002919	ORPHA:2089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0003076	ORPHA:2089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0011998	ORPHA:2089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0012734	ORPHA:2089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0001250	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0001254	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0001263	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0001508	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0002910	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0003077	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0004322	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency		HP:0011024	ORPHA:2089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0001508	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0001947	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0002148	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0003109	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0004919	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0006568	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0040270	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0500030	ORPHA:2088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0001510	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0001942	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0002150	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0002240	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0002748	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0003076	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0003162	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0003270	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0011998	ORPHA:2088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0000112	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0000121	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0000819	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0000938	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0001399	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0002155	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0002909	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0003155	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0006487	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0020110	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0031956	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0031964	ORPHA:2088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0000295	ORPHA:2088	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2088	Fanconi-Bickel syndrome		HP:0001402	ORPHA:2088	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0001263	ORPHA:542306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0001626	ORPHA:542306	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0000512	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0000639	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0000750	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0001250	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0001252	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0001344	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0001662	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0002020	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0005155	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0010864	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0011675	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0011704	ORPHA:542306	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0000546	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0000563	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0000817	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0001655	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0002421	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0002521	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0007010	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542306	GNB5-related intellectual disability-cardiac arrhythmia syndrome		HP:0012248	ORPHA:542306	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0003468	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0003508	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0005280	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0008064	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0008404	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0030055	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0001903	ORPHA:99688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0003355	ORPHA:99688	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0003196	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0000400	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0000581	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0000966	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0001249	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0001250	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0002007	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0002251	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99688	Dermotrichic syndrome		HP:0002353	ORPHA:99688	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0000252	ORPHA:391646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0000924	ORPHA:391646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0001249	ORPHA:391646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0005819	ORPHA:391646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0012758	ORPHA:391646	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0001156	ORPHA:391646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0001770	ORPHA:391646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0001999	ORPHA:391646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0004322	ORPHA:391646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0005235	ORPHA:391646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0009778	ORPHA:391646	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0000708	ORPHA:391646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0000712	ORPHA:391646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0000739	ORPHA:391646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0000712	ORPHA:391646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:391646	Feingold syndrome type 2		HP:0001629	ORPHA:391646	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0000988	ORPHA:448237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0040186	ORPHA:448237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0000509	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0000989	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001369	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001945	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0002315	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0002829	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0002921	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0003326	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0003496	ORPHA:448237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0000969	ORPHA:448237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001225	ORPHA:448237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001785	ORPHA:448237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0002013	ORPHA:448237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0012779	ORPHA:448237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0000252	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0000533	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0000612	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001132	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001287	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001511	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001873	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0001933	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0002383	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0005268	ORPHA:448237	TAS		HP:0040284			C	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0006906	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0007131	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0007401	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0007766	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0007814	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0012486	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0012795	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:448237	Zika virus disease		HP:0030825	ORPHA:448237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0000168	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0000179	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0000199	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0001061	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0001072	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0001482	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0001609	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0008066	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0011830	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0100699	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0200034	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0200039	ORPHA:530	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0000171	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0000218	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0000962	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0001332	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0002015	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0002205	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0002293	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0200043	ORPHA:530	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0001250	ORPHA:530	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0002514	ORPHA:530	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:530	Lipoid proteinosis		HP:0100582	ORPHA:530	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0002073	ORPHA:284324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0000641	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0000651	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0000657	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0000666	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0001152	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0001260	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0001272	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0001310	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0001347	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0002070	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0002136	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0002168	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0002312	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0001288	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0002495	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0003487	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0007240	ORPHA:284324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0002174	ORPHA:284324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia		HP:0003445	ORPHA:284324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284324	Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia	NOT	HP:0001250	ORPHA:284324	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0000112	ORPHA:531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0000177	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0000286	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0000348	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0000463	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0000960	ORPHA:531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0001250	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0001251	ORPHA:531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0001339	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0001510	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0001539	ORPHA:531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0001561	ORPHA:531	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0001626	ORPHA:531	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0002079	ORPHA:531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0002120	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0002353	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0003196	ORPHA:531	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:531	Miller-Dieker syndrome		HP:0004209	ORPHA:531	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0000857	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0001274	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0001360	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0001511	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0001518	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0011467	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0012443	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0030795	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0031209	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0100801	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0410289	ORPHA:556955	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0000218	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0000269	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0000340	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0000369	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0000377	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0000601	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0002507	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0006315	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0009658	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0010669	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0010938	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556955	Pancreatic agenesis-holoprosencephaly syndrome		HP:0012418	ORPHA:556955	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000037	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000175	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000347	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000369	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0001511	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0001671	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0030680	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0100335	ORPHA:2075	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000028	ORPHA:2075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000047	ORPHA:2075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000494	ORPHA:2075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0008668	ORPHA:2075	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000003	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000238	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000252	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000316	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000431	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0000776	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0001156	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0001162	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0002650	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0002714	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0002808	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0005264	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2075	Genitopalatocardiac syndrome		HP:0100016	ORPHA:2075	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000160	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000218	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000232	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000286	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000316	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000337	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000340	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000343	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000347	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000358	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000490	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000581	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0000995	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0001256	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0001629	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0001643	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0001770	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0001863	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0002002	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0002263	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0002553	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0003196	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0005280	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0005338	ORPHA:261120	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261120	14q11.2 microdeletion syndrome		HP:0011344	ORPHA:261120	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0000035	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0000407	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0000823	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0001053	ORPHA:2074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0001249	ORPHA:2074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0001251	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0001347	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0003202	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0003457	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0004322	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0004374	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0007328	ORPHA:2074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2074	Gemignani syndrome		HP:0008736	ORPHA:2074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0007018	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0007686	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0012452	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0025235	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0030014	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0040307	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000711	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000716	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000826	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0001279	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0001350	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000738	ORPHA:2073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0001262	ORPHA:2073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0002360	ORPHA:2073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0002524	ORPHA:2073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0010534	ORPHA:2073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000017	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000739	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000822	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000975	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0002019	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0002307	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0002494	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0002519	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0006896	ORPHA:2073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0001513	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0002076	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0010535	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0025233	ORPHA:2073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2073	Narcolepsy type 1		HP:0000709	ORPHA:2073	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001510	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001650	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001653	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001714	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001718	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001744	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001761	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001822	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001876	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001903	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002079	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002119	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002206	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002315	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0004406	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0007018	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000027	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000248	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000508	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000570	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000605	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000767	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000974	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001081	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001270	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001276	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002040	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002070	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002092	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0002650	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0005619	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0006530	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0006689	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0010543	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0011968	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0025160	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0031364	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0200042	ORPHA:2072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001433	ORPHA:2072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001873	ORPHA:2072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0003656	ORPHA:2072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0004380	ORPHA:2072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0004382	ORPHA:2072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0004963	ORPHA:2072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0007957	ORPHA:2072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000238	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000407	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000486	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000602	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0000657	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001249	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001250	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001258	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001265	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001288	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2072	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome		HP:0001347	ORPHA:2072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0001880	ORPHA:2070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0001903	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0001974	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002013	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002014	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002015	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002024	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002027	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002570	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0003073	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0003193	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0011024	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0011227	ORPHA:2070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0000969	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0001047	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0001541	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0001824	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002099	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002243	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0002573	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2070	Eosinophilic gastroenteritis		HP:0003565	ORPHA:2070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0002352	ORPHA:542310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0002514	ORPHA:542310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0010576	ORPHA:542310	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0000712	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001250	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001251	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001268	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001332	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0002135	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0002461	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0007229	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0007256	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0007346	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0100320	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0100543	ORPHA:542310	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001257	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001260	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001263	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001288	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001297	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001337	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0001342	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0002516	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0007291	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0011153	ORPHA:542310	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts		HP:0000725	ORPHA:542310	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542310	Leukoencephalopathy with calcifications and cysts	NOT	HP:0002059	ORPHA:542310	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0002589	ORPHA:436252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0004430	ORPHA:436252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0010766	ORPHA:436252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0011100	ORPHA:436252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0001511	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0001561	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0002223	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0002721	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0003270	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0005229	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0008070	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0025085	ORPHA:436252	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0000778	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0001072	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0002293	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0002566	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0002722	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0005224	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0100592	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0100889	ORPHA:436252	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0000872	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0001539	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0001629	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0001890	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0002960	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0003765	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0008404	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0010959	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0012115	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:436252	Combined immunodeficiency-multiple intestinal atresia		HP:0100651	ORPHA:436252	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000272	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000303	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000478	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000482	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000504	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000768	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000926	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000939	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000963	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0000974	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001252	ORPHA:2078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001256	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001263	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001510	ORPHA:2078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001582	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001763	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001883	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0002650	ORPHA:2078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0002757	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0002827	ORPHA:2078	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0002953	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0003312	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0003510	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0004568	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0004586	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0001382	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0005930	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0007495	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0011849	ORPHA:2078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2078	Geroderma osteodysplastica		HP:0100790	ORPHA:2078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000028	ORPHA:2077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000062	ORPHA:2077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000194	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000202	ORPHA:2077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000218	ORPHA:2077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000232	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000248	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000268	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000347	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000348	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000364	ORPHA:2077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000431	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000470	ORPHA:2077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000486	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000494	ORPHA:2077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000534	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0000664	ORPHA:2077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0001004	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0001249	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0001252	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0001263	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0001376	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0001636	ORPHA:2077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0001671	ORPHA:2077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0002015	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0002167	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0002375	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0002804	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0004322	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0005280	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0011800	ORPHA:2077	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2077	German syndrome		HP:0100490	ORPHA:2077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0000508	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0000577	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0001260	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0001270	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0001284	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0001349	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0001763	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0002151	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0002166	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0002312	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0002359	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0002380	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0003376	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0003444	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0007178	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0007340	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0009027	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0009055	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect		HP:0010836	ORPHA:521411	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect	NOT	HP:0001638	ORPHA:521411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:521411	Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect	NOT	HP:0040081	ORPHA:521411	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0000083	ORPHA:526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0000112	ORPHA:526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0000822	ORPHA:526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0001324	ORPHA:526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0002019	ORPHA:526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0002637	ORPHA:526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0002900	ORPHA:526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0011675	ORPHA:526	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:526	Liddle syndrome		HP:0012378	ORPHA:526	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529	Roch-Leri mesosomatous lipomatosis		HP:0001482	ORPHA:529	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:529	Roch-Leri mesosomatous lipomatosis		HP:0001012	ORPHA:529	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:529	Roch-Leri mesosomatous lipomatosis		HP:0000979	ORPHA:529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:529	Roch-Leri mesosomatous lipomatosis		HP:0001873	ORPHA:529	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000855	ORPHA:528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0002240	ORPHA:528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0003712	ORPHA:528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0008887	ORPHA:528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0009125	ORPHA:528	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000819	ORPHA:528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000998	ORPHA:528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001249	ORPHA:528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0002155	ORPHA:528	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000158	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000294	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000303	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000336	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000842	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000956	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001015	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001176	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001263	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001394	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001397	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001508	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001635	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001639	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001833	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0001999	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0002162	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0003124	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0003247	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0005616	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0008665	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0011407	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0012062	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0030796	ORPHA:528	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000141	ORPHA:528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000147	ORPHA:528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0000876	ORPHA:528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:528	Congenital generalized lipodystrophy		HP:0010465	ORPHA:528	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0000131	ORPHA:523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0000518	ORPHA:523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0000989	ORPHA:523	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0002891	ORPHA:523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0003011	ORPHA:523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0006732	ORPHA:523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0007437	ORPHA:523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0007620	ORPHA:523	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0100580	ORPHA:523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0100650	ORPHA:523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:523	Hereditary leiomyomatosis and renal cell cancer		HP:0100751	ORPHA:523	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0000962	ORPHA:525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0000989	ORPHA:525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0001053	ORPHA:525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0001059	ORPHA:525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0001231	ORPHA:525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0001596	ORPHA:525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0001806	ORPHA:525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0002242	ORPHA:525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0004334	ORPHA:525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0008066	ORPHA:525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0012115	ORPHA:525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0100649	ORPHA:525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0100725	ORPHA:525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0200034	ORPHA:525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525	Lichen planopilaris		HP:0200042	ORPHA:525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002664	ORPHA:524	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0003002	ORPHA:524	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0001909	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002665	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002669	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002859	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002888	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0006744	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0007378	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0009592	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0012126	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0012174	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0030070	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0030392	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0100006	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0200063	ORPHA:524	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002861	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002863	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002885	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002890	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0002894	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0003003	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0004808	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0006721	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0009726	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0010788	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0012125	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0012189	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0012288	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0012539	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0100526	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0100605	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0100615	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0100743	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:524	Li-Fraumeni syndrome		HP:0100768	ORPHA:524	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000023	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000047	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000126	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000175	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000202	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000235	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000238	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000256	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000269	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000316	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000329	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000347	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000369	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000384	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000431	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000470	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000494	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000501	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000567	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000612	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000648	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000835	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0000921	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001156	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001161	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001195	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001249	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001252	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001263	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001305	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001522	ORPHA:7	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001629	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001631	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001633	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001636	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001642	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001650	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001702	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0001804	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002007	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002020	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002023	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002119	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002167	ORPHA:7	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002205	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002269	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002566	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002650	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002705	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002808	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0002937	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0003196	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0003272	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0004322	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0004383	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0004397	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0005280	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0006101	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0006695	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0006709	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0007360	ORPHA:7	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0008736	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0008872	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:7	3C syndrome		HP:0008897	ORPHA:7	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0001945	ORPHA:31205	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0000988	ORPHA:31205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0001369	ORPHA:31205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0002013	ORPHA:31205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0002829	ORPHA:31205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0012282	ORPHA:31205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0001824	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0002014	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0002315	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0002374	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0002840	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0003095	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0003326	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0003418	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0012219	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0025143	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0025145	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0025439	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0040186	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0040189	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0040313	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0100806	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0200039	ORPHA:31205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0001287	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0001701	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0001733	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0001903	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0011850	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0012819	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0025181	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0025230	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31205	Rat-bite fever		HP:0100584	ORPHA:31205	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000098	ORPHA:8	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000272	ORPHA:8	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000369	ORPHA:8	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000750	ORPHA:8	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001270	ORPHA:8	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000256	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000316	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000708	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0012760	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000752	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000805	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001249	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001319	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001328	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001337	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001763	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0002099	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0007018	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0007642	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0040019	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0100710	ORPHA:8	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000027	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000028	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000047	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000053	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000054	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000238	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000303	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000729	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000739	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000798	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0000837	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001250	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0001572	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0002195	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0002363	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0003251	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0007033	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0010865	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0012871	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0030088	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0040183	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0100033	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0100851	ORPHA:8	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:8	47,XYY syndrome		HP:0008770	ORPHA:8	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0005547	ORPHA:521	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001744	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001871	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001873	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001894	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001911	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001912	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001945	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0001974	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0004396	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521	Chronic myeloid leukemia		HP:0012378	ORPHA:521	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000613	ORPHA:5	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001943	ORPHA:5	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001985	ORPHA:5	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000512	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000572	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000577	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001252	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001263	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001639	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001939	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0002240	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0009830	ORPHA:5	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000488	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000532	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000533	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000545	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0000662	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001249	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001250	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001290	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0001508	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0002611	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0007703	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0011968	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:5	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency		HP:0030856	ORPHA:5	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0001252	ORPHA:6	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0001257	ORPHA:6	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0001531	ORPHA:6	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0001943	ORPHA:6	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0001987	ORPHA:6	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0001992	ORPHA:6	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0002093	ORPHA:6	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0004357	ORPHA:6	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0100022	ORPHA:6	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:6	3-methylcrotonyl-CoA carboxylase deficiency		HP:0100659	ORPHA:6	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0000225	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0000421	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0000967	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0000978	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0000979	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001324	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001824	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001873	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001876	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001882	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001892	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001903	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001945	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0002039	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0002321	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0002875	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0005521	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0012378	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0031020	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0031035	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0031364	ORPHA:520	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0000212	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001875	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0001974	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0002027	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0002653	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0002716	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0010280	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0011900	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0025420	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0030140	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0030955	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0031245	ORPHA:520	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0000790	ORPHA:520	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0100608	ORPHA:520	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:520	Acute promyelocytic leukemia		HP:0100758	ORPHA:520	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0001649	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0001945	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0001974	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0002090	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0002315	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0002829	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0003326	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0010702	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0025143	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0025406	ORPHA:3392	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0000155	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0000988	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0001873	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0001903	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0002098	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0002113	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0002202	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0002716	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0011355	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0012735	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0025289	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0025439	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0030833	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0031983	ORPHA:3392	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0000388	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0000509	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0000707	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0000708	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0001287	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0001289	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0012219	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0030049	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0030953	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0031292	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0100533	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0100721	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:0200026	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3392	Tularemia		HP:3000033	ORPHA:3392	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000218	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000243	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000248	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000272	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000316	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000343	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000347	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000369	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000463	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000465	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000470	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000581	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001249	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001263	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001816	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0002162	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0005280	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0006610	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0007477	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0008551	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0009623	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0009738	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0009892	ORPHA:261112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000028	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000047	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000062	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000160	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000164	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000252	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000286	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000486	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000574	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000582	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000639	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000664	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001250	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001252	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001276	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001376	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001850	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0002553	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0002650	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0003196	ORPHA:261112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000074	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000175	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000413	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000453	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000494	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000568	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000772	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000776	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0000925	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001162	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001274	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0001362	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0007598	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0030680	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261112	Monosomy 9p syndrome		HP:0100790	ORPHA:261112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000028	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000062	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000215	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000218	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000252	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000286	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000347	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000400	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000431	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001249	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001252	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001263	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001276	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0002060	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0002079	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0002365	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0002380	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0002500	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0003202	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0006955	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0030197	ORPHA:284339	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000054	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000133	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000151	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000582	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000639	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0000648	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001250	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001257	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001336	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0001347	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0004305	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0005280	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0008665	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0012856	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0030260	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284339	Pontocerebellar hypoplasia type 7		HP:0030261	ORPHA:284339	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0001945	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0002090	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0011947	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0011949	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0025044	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0031273	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0031864	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0100806	ORPHA:31202	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0001743	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0002758	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0003095	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0012115	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0025059	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0030049	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0031292	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0032162	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0100523	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0100658	ORPHA:31202	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0000024	ORPHA:31202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0000119	ORPHA:31202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0000197	ORPHA:31202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0001886	ORPHA:31202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31202	Melioidosis		HP:0011850	ORPHA:31202	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0000164	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0000286	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0000316	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0000486	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0000582	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0001252	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0001263	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0001328	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0002974	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0001382	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0100543	ORPHA:9	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0001156	ORPHA:9	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0001385	ORPHA:9	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0004209	ORPHA:9	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0010978	ORPHA:9	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0030680	ORPHA:9	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:9	Tetrasomy X syndrome		HP:0008209	ORPHA:9	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0001945	ORPHA:31204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002090	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002094	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002721	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0012378	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0031245	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0031864	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0032016	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0100749	ORPHA:31204	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0000509	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0000620	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0001482	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0001701	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0001824	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002013	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002039	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002097	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002098	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002102	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002105	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002107	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002202	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002315	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002754	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002840	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002878	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0004372	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0011450	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0025143	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0030049	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0030166	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0031246	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0031292	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0032169	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0100523	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0100806	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0200026	ORPHA:31204	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0000491	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0000575	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0000834	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0001250	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0001287	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0001654	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002383	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0002586	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0004302	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0012424	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0045026	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0100532	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0100584	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0100646	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:31204	Nocardiosis		HP:0100658	ORPHA:31204	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2064	Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome		HP:0000508	ORPHA:2064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2064	Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome		HP:0000960	ORPHA:2064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2064	Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome		HP:0001387	ORPHA:2064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2064	Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome		HP:0003312	ORPHA:2064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2064	Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome		HP:0005626	ORPHA:2064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2064	Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome		HP:0008368	ORPHA:2064	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000023	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000951	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0001385	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0001622	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0002815	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0002817	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0002823	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0002991	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0003019	ORPHA:2063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000028	ORPHA:2063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000347	ORPHA:2063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0100559	ORPHA:2063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0100560	ORPHA:2063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000174	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000189	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000358	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0000776	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0001250	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0001357	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0002023	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0002101	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0002269	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0006283	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0006333	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0006703	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0009804	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0030680	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2063	Splenogonadal fusion-limb defects-micrognathia syndrome		HP:0100543	ORPHA:2063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000154	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000233	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000248	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000311	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000316	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000322	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000347	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000431	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000494	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000925	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0001072	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0001176	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0002650	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0002808	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0002937	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0005108	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0005280	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0012368	ORPHA:2062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0000098	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0001387	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0001999	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0002011	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0002653	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0003306	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0003363	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0005037	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2062	Progressive non-infectious anterior vertebral fusion		HP:0100777	ORPHA:2062	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0002073	ORPHA:284332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0000750	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001257	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001260	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001263	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001272	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001290	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001310	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001347	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001763	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0002136	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0002312	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0001288	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0003487	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0004322	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0006855	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0007240	ORPHA:284332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284332	Infantile-onset autosomal recessive nonprogressive cerebellar ataxia		HP:0002080	ORPHA:284332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000430	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000510	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000529	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0001118	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0001263	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0001999	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0002342	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0004322	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0007675	ORPHA:436245	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000272	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000347	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000369	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000470	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000582	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000689	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000699	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0001133	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0001156	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0001328	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0002311	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0007010	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0007791	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0007965	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0009907	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0010761	ORPHA:436245	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000400	ORPHA:436245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436245	Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome		HP:0000494	ORPHA:436245	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0000316	ORPHA:2069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0000486	ORPHA:2069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0000545	ORPHA:2069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0000582	ORPHA:2069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0000664	ORPHA:2069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0000995	ORPHA:2069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0001003	ORPHA:2069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0001677	ORPHA:2069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0002036	ORPHA:2069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0004398	ORPHA:2069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0005280	ORPHA:2069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0005978	ORPHA:2069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2069	Gastrocutaneous syndrome		HP:0007565	ORPHA:2069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0001945	ORPHA:542323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0011112	ORPHA:542323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0011117	ORPHA:542323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0012378	ORPHA:542323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0012649	ORPHA:542323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0001649	ORPHA:542323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002615	ORPHA:542323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0003326	ORPHA:542323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0004396	ORPHA:542323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0030356	ORPHA:542323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0030783	ORPHA:542323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0001289	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002013	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002014	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002018	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002202	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002789	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002904	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002910	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0003259	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0011037	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0011675	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0012418	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0012664	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0012722	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0030005	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0100598	ORPHA:542323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0000988	ORPHA:542323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0001919	ORPHA:542323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0002878	ORPHA:542323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:542323	CAR T cell therapy-associated cytokine release syndrome		HP:0005521	ORPHA:542323	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000232	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000316	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000337	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000343	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000347	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000348	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000369	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000463	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000653	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000684	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000974	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0001596	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0002007	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0002234	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0002750	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0004322	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0005280	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0001382	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0007495	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0009891	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0009928	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0011800	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0045075	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0100540	ORPHA:2067	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000174	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000303	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000501	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000505	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000563	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000765	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000889	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000944	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0001537	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0002644	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0003312	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0010609	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0100659	ORPHA:2067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000135	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000141	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000365	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000453	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000545	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000639	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000648	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000787	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0000798	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0001028	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0001053	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0001510	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0001555	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0002516	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0002621	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0004331	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2067	GAPO syndrome		HP:0100607	ORPHA:2067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0200134	ORPHA:2066	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001252	ORPHA:2066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0002353	ORPHA:2066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0007266	ORPHA:2066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0011344	ORPHA:2066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0032531	ORPHA:2066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0410053	ORPHA:2066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0500253	ORPHA:2066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0000098	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0000845	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001250	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001266	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001347	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001508	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0002059	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0007272	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0008872	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0025430	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0100786	ORPHA:2066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001254	ORPHA:2066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001272	ORPHA:2066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2066	Gamma-aminobutyric acid transaminase deficiency		HP:0001273	ORPHA:2066	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000093	ORPHA:2065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000100	ORPHA:2065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000112	ORPHA:2065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000164	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000252	ORPHA:2065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000316	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000347	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000400	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0000601	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001181	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001250	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001252	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001263	ORPHA:2065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001276	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001302	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001511	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0001622	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0002036	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0002269	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0002353	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0002410	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0004322	ORPHA:2065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0004374	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0005108	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0010978	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0100490	ORPHA:2065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0100543	ORPHA:2065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2065	Galloway-Mowat syndrome		HP:0100720	ORPHA:2065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0001873	ORPHA:517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0001903	ORPHA:517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0001974	ORPHA:517	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0000980	ORPHA:517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0001824	ORPHA:517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0001892	ORPHA:517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0002094	ORPHA:517	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0000168	ORPHA:517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:517	Acute myelomonocytic leukemia		HP:0001880	ORPHA:517	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0006970	ORPHA:512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0012379	ORPHA:512	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000365	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000505	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000649	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000762	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001250	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001251	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001265	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001288	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001324	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002191	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002359	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002376	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002922	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0003394	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0008947	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0009830	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0030890	ORPHA:512	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000020	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000708	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000709	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000712	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000726	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0000751	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001260	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001332	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0001337	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002311	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002607	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0009763	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0011471	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0011968	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0012531	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0030051	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0030858	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0031064	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0100753	ORPHA:512	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002246	ORPHA:512	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002576	ORPHA:512	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0002577	ORPHA:512	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0012437	ORPHA:512	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0025013	ORPHA:512	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0100575	ORPHA:512	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:512	Metachromatic leukodystrophy		HP:0100762	ORPHA:512	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0000600	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0001249	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0001250	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0001251	ORPHA:511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0001252	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0001263	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0001315	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0001608	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0002093	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0004374	ORPHA:511	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:511	Maple syrup urine disease		HP:0008344	ORPHA:511	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0000253	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0000338	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001249	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001257	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001263	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001272	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001300	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001332	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001337	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0001347	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002059	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002067	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002376	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002465	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002483	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002505	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002650	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0002828	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0003487	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0008936	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0011448	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0012048	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0012407	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0030890	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0032097	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521406	Dystonia-parkinsonism-hypermanganesemia syndrome		HP:0100660	ORPHA:521406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0004845	ORPHA:514	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001903	ORPHA:514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001974	ORPHA:514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0002875	ORPHA:514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0012378	ORPHA:514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0031020	ORPHA:514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0100827	ORPHA:514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001482	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001730	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001785	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001824	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001931	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0001945	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0002039	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0011787	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0012145	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0025289	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0025435	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0100520	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:514	Acute monoblastic/monocytic leukemia		HP:0100539	ORPHA:514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0000750	ORPHA:261102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0001256	ORPHA:261102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0004942	ORPHA:261102	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0000028	ORPHA:261102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0000729	ORPHA:261102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0000739	ORPHA:261102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0000776	ORPHA:261102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0001252	ORPHA:261102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0007018	ORPHA:261102	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0000238	ORPHA:261102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0001643	ORPHA:261102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0002308	ORPHA:261102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0007330	ORPHA:261102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:261102	Distal 7q11.23 microduplication syndrome		HP:0100835	ORPHA:261102	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0001394	ORPHA:402823	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0012115	ORPHA:402823	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0031964	ORPHA:402823	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0000952	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0000978	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0001289	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0001399	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0001892	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0001945	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0002017	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0002027	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0002039	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0004396	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0004787	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0012378	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0031956	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0033834	ORPHA:402823	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:402823	Hepatitis delta		HP:0001402	ORPHA:402823	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0000099	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0000218	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0000303	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0001166	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0001382	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0001519	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0002119	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0002342	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0002942	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0011451	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2172	Microcephaly-glomerulonephritis-marfanoid habitus syndrome		HP:0012622	ORPHA:2172	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0000763	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0000835	ORPHA:230839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0000963	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0000974	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0000978	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0001252	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0001297	ORPHA:230839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0001324	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0001382	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0001634	ORPHA:230839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0002239	ORPHA:230839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0002829	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0003202	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0003298	ORPHA:230839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0003326	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0003701	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0004416	ORPHA:230839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0001382	ORPHA:230839	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0009830	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0011675	ORPHA:230839	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230839	Classical-like Ehlers-Danlos syndrome type 1		HP:0012378	ORPHA:230839	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0000618	ORPHA:2177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0001263	ORPHA:2177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0001511	ORPHA:2177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0002120	ORPHA:2177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0008610	ORPHA:2177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0008897	ORPHA:2177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0010994	ORPHA:2177	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0000601	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0001250	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0001254	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0001264	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0001287	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0002179	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0006698	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0007023	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0009145	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0010652	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0011328	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0025040	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0025099	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0025258	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0025517	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0410279	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:3000062	ORPHA:2177	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0000533	ORPHA:2177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0000609	ORPHA:2177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0002119	ORPHA:2177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2177	Hydranencephaly		HP:0011451	ORPHA:2177	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000147	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000212	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000256	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000280	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000470	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000834	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000938	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000939	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0000953	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001004	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001025	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001072	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001156	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001252	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001387	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001482	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001508	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0001510	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002024	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002028	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002570	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002659	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002718	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002721	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002749	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002757	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0002983	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0003011	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0003510	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0004279	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0006482	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0010515	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0011024	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0011968	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0100490	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0100585	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2176	Infantile systemic hyalinosis		HP:0200042	ORPHA:2176	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001249	ORPHA:468678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001263	ORPHA:468678	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000252	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000316	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000505	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000540	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000729	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000750	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000752	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001256	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001513	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001999	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002360	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0004322	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0006863	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0008872	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0008947	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0011024	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0011968	ORPHA:468678	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000160	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000194	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000219	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000248	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000307	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000356	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000407	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000483	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000486	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000510	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000545	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000718	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000733	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001250	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001344	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002020	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002353	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0010864	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0011800	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0012450	ORPHA:468678	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000023	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000081	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000218	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000272	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000297	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000322	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000358	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000455	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000470	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000612	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000618	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000648	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000722	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0000776	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001045	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001272	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001382	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0001627	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002079	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002120	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002188	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002280	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002311	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002373	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002384	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002714	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002870	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0002933	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0005280	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0012110	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0012157	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0012448	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468678	White-Sutton syndrome		HP:0100716	ORPHA:468678	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0002803	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0002817	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0007370	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0008872	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0010483	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0010741	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0010742	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0410030	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:5201015	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0000238	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0000316	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0002814	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0009775	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0010491	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0010495	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0010721	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0011220	ORPHA:295000	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0000175	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0000589	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0001263	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0001539	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0001543	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0001558	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0001622	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0001683	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0001762	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0002084	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295000	Amniotic band syndrome		HP:0002650	ORPHA:295000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0003477	ORPHA:468661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0007020	ORPHA:468661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0000505	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0001123	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0001761	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0001288	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0003445	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0003693	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0007067	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0007083	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0008314	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0009053	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0009072	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0011923	ORPHA:468661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0000648	ORPHA:468661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0003487	ORPHA:468661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0001272	ORPHA:468661	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0002079	ORPHA:468661	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:468661	Autosomal recessive spastic paraplegia type 74		HP:0012762	ORPHA:468661	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0000248	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0000252	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0000286	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0000324	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0000486	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0000582	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0000601	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0001156	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0001252	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0001357	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0001360	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0001363	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0002673	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0002750	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0004209	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0004322	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0007703	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0008479	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0009882	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0012745	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2163	Holoprosencephaly-craniosynostosis syndrome		HP:0100543	ORPHA:2163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000028	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000079	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000093	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000161	ORPHA:2162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000238	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000252	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000256	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000286	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000289	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000316	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000400	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000437	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000453	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000457	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000458	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000463	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000470	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000488	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000490	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000508	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000528	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000567	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000568	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000574	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000581	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000582	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000601	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000612	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000648	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000664	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000776	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000819	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000830	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000871	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000873	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000929	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001156	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001161	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001250	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001252	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001257	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001263	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001305	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001324	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001332	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001360	ORPHA:2162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001531	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001539	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001629	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001636	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001641	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001679	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001743	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001883	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001943	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001999	ORPHA:2162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002002	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002007	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002019	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002020	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002072	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002084	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002093	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002269	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002553	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002650	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0002902	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0003312	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0004409	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0005469	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0001382	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0006315	ORPHA:2162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0006703	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0007360	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0007370	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0009099	ORPHA:2162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0000377	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0008736	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0008872	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0009738	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0009794	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0009804	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0009914	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0009924	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0010301	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0010302	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0010669	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0011100	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0011675	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0012639	ORPHA:2162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0100336	ORPHA:2162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0100543	ORPHA:2162	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2162	Holoprosencephaly		HP:0100596	ORPHA:2162	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000974	ORPHA:230851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001382	ORPHA:230851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001653	ORPHA:230851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001654	ORPHA:230851	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000023	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000486	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000508	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000545	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000678	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000767	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000963	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000978	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001027	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001058	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001075	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001373	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001659	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001763	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001822	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0002616	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0002816	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0002857	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0005180	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0006109	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0006201	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0100807	ORPHA:230851	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000218	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000414	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0000574	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001250	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001263	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001519	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001631	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001634	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001712	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001848	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0001852	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0002094	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0002342	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0002751	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0002944	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0004322	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0010444	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0012378	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0012717	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0031610	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0032523	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0100550	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:230851	Cardiac-valvular Ehlers-Danlos syndrome		HP:0500041	ORPHA:230851	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001263	ORPHA:2169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001980	ORPHA:2169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002160	ORPHA:2169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000252	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000478	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001249	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001250	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001252	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001508	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001511	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001972	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002013	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002167	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002329	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002500	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0003658	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0005518	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0007185	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0008897	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0011344	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0011968	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0012444	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0100022	ORPHA:2169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000238	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000365	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000505	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000639	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000708	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000822	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000924	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0000939	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001159	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001254	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001262	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001392	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001626	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001875	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001876	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0001907	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002119	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002365	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002625	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0002650	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0005575	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0006895	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0009830	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0012448	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0012704	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0030084	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2169	Methylcobalamin deficiency type cblE		HP:0100820	ORPHA:2169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0000175	ORPHA:2167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0001161	ORPHA:2167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0001511	ORPHA:2167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0001562	ORPHA:2167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0006703	ORPHA:2167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0008678	ORPHA:2167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0030680	ORPHA:2167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0000262	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0000358	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0000400	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0000465	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0000772	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0001195	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0001387	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0005916	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0007370	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0010295	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0010297	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0040071	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0100016	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2167	Holzgreve syndrome		HP:0100569	ORPHA:2167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000568	ORPHA:2166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000601	ORPHA:2166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001162	ORPHA:2166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0008736	ORPHA:2166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0010650	ORPHA:2166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000028	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000047	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000062	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000175	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000202	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000238	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000252	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000358	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000835	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000864	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001252	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001360	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001671	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0002023	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0002101	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0005990	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0007370	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0030680	ORPHA:2166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000160	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0000347	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001321	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001537	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001539	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001561	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0001883	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0002084	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0002566	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0008678	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0009914	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0100542	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2166	Holoprosencephaly-postaxial polydactyly syndrome		HP:0100596	ORPHA:2166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000078	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000083	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000161	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000175	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000252	ORPHA:2165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000316	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000369	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000520	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0000924	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0001360	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0001622	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0002818	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0006433	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0009914	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0010662	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2165	Holoprosencephaly-caudal dysgenesis syndrome		HP:0100659	ORPHA:2165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0000656	ORPHA:411777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0000989	ORPHA:411777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0200034	ORPHA:411777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0000481	ORPHA:411777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0000509	ORPHA:411777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0001097	ORPHA:411777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0001609	ORPHA:411777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411777	Generalized eruptive keratoacanthoma		HP:0002015	ORPHA:411777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0001511	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0002134	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0002310	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0003273	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0003548	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0003554	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0003803	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0006466	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0006895	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0011471	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0011968	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0040204	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0002151	ORPHA:319514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0200125	ORPHA:319514	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0000407	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0000639	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0001266	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0001290	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0001324	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0002421	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0002451	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0002490	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0007069	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0008936	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0010994	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0012448	ORPHA:319514	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0000496	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0000519	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0000762	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0000763	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0001273	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0001344	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319514	Combined oxidative phosphorylation defect type 13		HP:0001508	ORPHA:319514	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001252	ORPHA:536545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001382	ORPHA:536545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0002751	ORPHA:536545	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000286	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000369	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000494	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000664	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000974	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000978	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000987	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001027	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001030	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001319	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0002194	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0008453	ORPHA:536545	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000023	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000218	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000365	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000407	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000482	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000545	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000592	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000767	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000938	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000963	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001058	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001155	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001166	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001324	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001328	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001342	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001374	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001519	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001537	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001558	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001760	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001762	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001763	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001288	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0002827	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0003202	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0003834	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0007023	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0007502	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0010727	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0011968	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0025019	ORPHA:536545	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000015	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000276	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000347	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000405	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000422	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000601	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000768	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0000939	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001647	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0001651	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0002650	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0003198	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0003467	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0003994	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0004322	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0004942	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0004976	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536545	Kyphoscoliotic Ehlers-Danlos syndrome		HP:0100309	ORPHA:536545	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000020	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000028	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000047	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000179	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000194	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000232	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000252	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000276	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000303	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000307	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000316	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000358	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000403	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000431	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000437	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000486	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000490	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000506	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000733	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000767	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000768	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001159	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001250	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001274	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001371	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001510	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001627	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001643	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001671	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001763	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001822	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002011	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002079	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002136	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002251	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002342	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002360	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002427	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002607	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002650	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002750	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002857	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0004322	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0004325	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0005274	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0007328	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0009487	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0009765	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0009909	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0010055	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0010511	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0010761	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0010845	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0010862	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0010864	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0011228	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0011229	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0012385	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0012758	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0031936	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0040082	ORPHA:2152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000003	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000075	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000076	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000077	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000125	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000126	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000212	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000405	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000478	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000480	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000483	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000518	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000545	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000568	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000612	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000639	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000678	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000684	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000687	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000692	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0012760	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000739	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001181	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001182	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001251	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001252	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001257	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001320	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001492	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001636	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001642	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001647	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001650	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001680	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001746	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001848	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002013	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002019	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002021	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002119	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002126	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002133	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002335	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002376	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002500	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002540	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002579	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002719	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0003763	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0004313	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0004387	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0006482	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0007042	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0007048	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0007165	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0007270	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0007359	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0010850	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0012081	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0025100	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0025156	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0032046	ORPHA:2152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000034	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000041	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000048	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000054	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000175	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000193	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000407	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0000876	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0001153	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002015	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002757	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0002777	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0004961	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0011326	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0030264	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0410005	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2152	Mowat-Wilson syndrome		HP:0410031	ORPHA:2152	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0000615	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0000975	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0001250	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0001657	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0002251	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0004375	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0006747	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2151	Hirschsprung disease-ganglioneuroblastoma syndrome		HP:0011675	ORPHA:2151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2150	Hirschsprung disease-type D brachydactyly syndrome		HP:0002251	ORPHA:2150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2150	Hirschsprung disease-type D brachydactyly syndrome		HP:0010624	ORPHA:2150	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2150	Hirschsprung disease-type D brachydactyly syndrome		HP:0001156	ORPHA:2150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2150	Hirschsprung disease-type D brachydactyly syndrome		HP:0001804	ORPHA:2150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2150	Hirschsprung disease-type D brachydactyly syndrome		HP:0009650	ORPHA:2150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2150	Hirschsprung disease-type D brachydactyly syndrome		HP:0010111	ORPHA:2150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0000708	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0000716	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0000726	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0000737	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0000752	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0001250	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0001251	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0001332	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0001347	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0001824	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002063	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002066	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002067	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002072	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002136	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002500	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0012547	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0030190	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0200147	ORPHA:248111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0001272	ORPHA:248111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0001336	ORPHA:248111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002073	ORPHA:248111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0002119	ORPHA:248111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:248111	Juvenile Huntington disease		HP:0006855	ORPHA:248111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0000343	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0000400	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0000407	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0000431	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0001249	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0001800	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0001943	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0002119	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0002120	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0002750	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0002927	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0005819	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0005844	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2158	Histidinuria-renal tubular defect syndrome		HP:0008666	ORPHA:2158	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002720	ORPHA:331206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002850	ORPHA:331206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0004313	ORPHA:331206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0004315	ORPHA:331206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0004429	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0010975	ORPHA:331206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0011839	ORPHA:331206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0001508	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0001888	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0001945	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002718	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002743	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002841	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0004385	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0031381	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0031402	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0045080	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0200117	ORPHA:331206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0000980	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0000988	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0001433	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0001873	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0001880	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0001890	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002240	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002840	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002910	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0002960	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331206	Severe combined immunodeficiency due to complete RAG1/2 deficiency		HP:0040089	ORPHA:331206	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2157	Histidinemia		HP:0002927	ORPHA:2157	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2157	Histidinemia		HP:0010906	ORPHA:2157	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2157	Histidinemia		HP:0000708	ORPHA:2157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2157	Histidinemia		HP:0000752	ORPHA:2157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2157	Histidinemia		HP:0001328	ORPHA:2157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2157	Histidinemia		HP:0002167	ORPHA:2157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2157	Histidinemia		HP:0011343	ORPHA:2157	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2155	Hirschsprung disease-deafness-polydactyly syndrome		HP:0001829	ORPHA:2155	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2155	Hirschsprung disease-deafness-polydactyly syndrome		HP:0002251	ORPHA:2155	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2155	Hirschsprung disease-deafness-polydactyly syndrome		HP:0000104	ORPHA:2155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2155	Hirschsprung disease-deafness-polydactyly syndrome		HP:0000316	ORPHA:2155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2155	Hirschsprung disease-deafness-polydactyly syndrome		HP:0000407	ORPHA:2155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2155	Hirschsprung disease-deafness-polydactyly syndrome		HP:0001162	ORPHA:2155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2155	Hirschsprung disease-deafness-polydactyly syndrome		HP:0001249	ORPHA:2155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0001288	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0003198	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0003376	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0003458	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0003557	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0003687	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0003805	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0008180	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0009027	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0009049	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0009058	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0031374	ORPHA:609	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0002312	ORPHA:609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0003731	ORPHA:609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0008994	ORPHA:609	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy		HP:0008959	ORPHA:609	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy	NOT	HP:0001638	ORPHA:609	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy	NOT	HP:0002878	ORPHA:609	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:609	Tibial muscular dystrophy	NOT	HP:0009077	ORPHA:609	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0003198	ORPHA:603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0003458	ORPHA:603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0008954	ORPHA:603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0008959	ORPHA:603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0009027	ORPHA:603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0009077	ORPHA:603	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0002312	ORPHA:603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0001288	ORPHA:603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0003376	ORPHA:603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0003805	ORPHA:603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0007149	ORPHA:603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type		HP:0008180	ORPHA:603	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:603	Distal myopathy, Welander type	NOT	HP:0001638	ORPHA:603	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0000518	ORPHA:606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0002486	ORPHA:606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0003202	ORPHA:606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0003326	ORPHA:606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0003327	ORPHA:606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0003701	ORPHA:606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0000407	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0002015	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0002019	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0002027	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0003552	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0004313	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0005978	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0007787	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0008189	ORPHA:606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0000026	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0000975	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0001262	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0001348	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0001638	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0002360	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0002870	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0002926	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0003077	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0008981	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0012378	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0012452	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0030319	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0031546	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:606	Proximal myotonic myopathy		HP:0100543	ORPHA:606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001260	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001283	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001347	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001430	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001604	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001609	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001611	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001621	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0002015	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0002317	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0001288	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0002460	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0002747	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0002835	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0003457	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0003738	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0003805	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0005934	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0007354	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0008180	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0008756	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0031374	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0430015	ORPHA:600	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0003547	ORPHA:600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0007149	ORPHA:600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0008049	ORPHA:600	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0000726	ORPHA:600	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0000762	ORPHA:600	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy		HP:0002936	ORPHA:600	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:600	Vocal cord and pharyngeal distal myopathy	NOT	HP:0009071	ORPHA:600	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003805	ORPHA:602	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0007340	ORPHA:602	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0008180	ORPHA:602	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0008963	ORPHA:602	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0009027	ORPHA:602	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0012548	ORPHA:602	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0100299	ORPHA:602	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0000821	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003376	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003438	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003458	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003547	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003557	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0006251	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0006467	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0012515	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0030007	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0100284	ORPHA:602	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0001324	ORPHA:602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0001436	ORPHA:602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003691	ORPHA:602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0003724	ORPHA:602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0007210	ORPHA:602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0010628	ORPHA:602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0040047	ORPHA:602	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0001638	ORPHA:602	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy		HP:0009077	ORPHA:602	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:602	GNE myopathy	NOT	HP:0003731	ORPHA:602	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001250	ORPHA:464282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001263	ORPHA:464282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0007020	ORPHA:464282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000316	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000407	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000490	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000545	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000556	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000750	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001249	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001251	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001257	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001260	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001332	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002061	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002123	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002317	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001288	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002515	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002650	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002714	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002808	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002827	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0008936	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0025313	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0031087	ORPHA:464282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000020	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0000252	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0001513	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002059	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002069	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0002079	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0004322	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0008373	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0010219	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0011166	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0011401	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome		HP:0012762	ORPHA:464282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome	NOT	HP:0001437	ORPHA:464282	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:464282	Spastic paraplegia-severe developmental delay-epilepsy syndrome	NOT	HP:0002380	ORPHA:464282	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3471	Young syndrome		HP:0000144	ORPHA:3471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3471	Young syndrome		HP:0002837	ORPHA:3471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3471	Young syndrome		HP:0005425	ORPHA:3471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3471	Young syndrome		HP:0011962	ORPHA:3471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3471	Young syndrome		HP:0001732	ORPHA:3471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0009881	ORPHA:3472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0010102	ORPHA:3472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0010107	ORPHA:3472	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000047	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000054	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000188	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000216	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000233	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000268	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000316	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000322	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000331	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000347	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000348	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000369	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000377	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000463	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000518	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000520	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000582	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000647	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000653	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000954	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001159	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001167	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001182	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001263	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001274	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001302	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001525	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001629	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001638	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001640	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001831	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001838	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001840	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002092	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002139	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002209	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002529	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002696	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002705	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0004322	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0004331	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0005793	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0005819	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0005989	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0006323	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0006628	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0006709	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0006710	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0007333	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0007633	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0008386	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0008897	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0008935	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0009381	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0009777	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0010035	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0010067	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0010537	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0011061	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0011451	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0012294	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0040163	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0045075	ORPHA:3472	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000028	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000059	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000162	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000238	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000365	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000568	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000773	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0000822	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001321	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001561	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001631	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001789	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001920	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002021	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0002827	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0003015	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0004993	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0006713	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0008665	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0010880	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0012809	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0030816	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0100817	ORPHA:3472	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3472	Yunis-Varon syndrome		HP:0001636	ORPHA:3472	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0000008	ORPHA:2141	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0000776	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0000782	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0001539	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0002089	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0002814	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0002817	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0002823	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0004209	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0004331	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0006101	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0006492	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0006495	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0006501	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0006507	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2141	Diaphragmatic defect-limb deficiency-skull defect syndrome		HP:0100560	ORPHA:2141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0001875	ORPHA:51636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0001888	ORPHA:51636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0011992	ORPHA:51636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0031020	ORPHA:51636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0031160	ORPHA:51636	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002090	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002718	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002788	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0004313	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0006532	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0011947	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0012740	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0200043	ORPHA:51636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0000246	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0000388	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0001636	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002070	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002110	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002167	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002172	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002244	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0007010	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0025439	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0030079	ORPHA:51636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0000166	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0001045	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0001250	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0001287	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0002840	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0011850	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0012056	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0100658	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0100750	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51636	WHIM syndrome		HP:0100806	ORPHA:51636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0000776	ORPHA:2140	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0000884	ORPHA:2140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0002089	ORPHA:2140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0002098	ORPHA:2140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0002566	ORPHA:2140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0010315	ORPHA:2140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0012418	ORPHA:2140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2140	Congenital diaphragmatic hernia		HP:0030680	ORPHA:2140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2149	Nodular neuronal heterotopia		HP:0001250	ORPHA:2149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2149	Nodular neuronal heterotopia		HP:0002269	ORPHA:2149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2149	Nodular neuronal heterotopia		HP:0002353	ORPHA:2149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0000708	ORPHA:2148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0001250	ORPHA:2148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002463	ORPHA:2148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0100543	ORPHA:2148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0001302	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0001371	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002197	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0003808	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0007015	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0007359	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0012469	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0012672	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0031882	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0100021	ORPHA:2148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0000713	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0000729	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0000737	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002015	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002079	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002339	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002521	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002650	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0002835	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0005484	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0006956	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0008872	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0012448	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0012520	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0012762	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2148	Lissencephaly type 1 due to doublecortin gene mutation		HP:0200134	ORPHA:2148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000175	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000248	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000262	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000272	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000316	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000347	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000444	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000465	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000772	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0000795	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0001156	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0001171	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0001363	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0001511	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0001562	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0002983	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0003196	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0004322	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0006101	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0006703	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0008551	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0009738	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0010935	ORPHA:2145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2145	Craniosynostosis, Herrmann-Opitz type		HP:0100543	ORPHA:2145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000093	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000130	ORPHA:2143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000256	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000260	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000316	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000337	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000349	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000358	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000407	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000494	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000520	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000529	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000541	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000545	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000556	ORPHA:2143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000612	ORPHA:2143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000776	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0000813	ORPHA:2143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0001249	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0001250	ORPHA:2143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0001263	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0001537	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0001539	ORPHA:2143	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0001629	ORPHA:2143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0002566	ORPHA:2143	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0003196	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0005280	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2143	Donnai-Barrow syndrome		HP:0007370	ORPHA:2143	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000169	ORPHA:3473	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000154	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000414	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000445	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001249	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001382	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001804	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001817	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0002265	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0004554	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0009102	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0009894	ORPHA:3473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000158	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000175	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000193	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000218	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000316	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000347	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000470	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000494	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000506	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000518	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000527	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000574	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000668	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000811	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000977	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001250	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001510	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001744	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001761	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001763	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001822	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0002219	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0002240	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0008947	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0011069	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0030680	ORPHA:3473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0000407	ORPHA:3473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0001869	ORPHA:3473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0006191	ORPHA:3473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0006391	ORPHA:3473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3473	Zimmermann-Laband syndrome		HP:0007440	ORPHA:3473	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000098	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000164	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000248	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000286	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000316	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000322	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000356	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000365	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000457	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000480	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000486	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000508	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000668	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000691	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0001249	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0006482	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0006709	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0007477	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0008064	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0010783	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0012471	ORPHA:3474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000175	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000582	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0001250	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0001636	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0001669	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0001773	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0004279	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0005930	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0006660	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0007957	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0009767	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0010173	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0010882	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0011069	ORPHA:3474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000077	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000126	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000717	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0000962	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0001629	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0002120	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0002213	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0002488	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0002797	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0002827	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0008070	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0100760	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3474	CHIME syndrome		HP:0200042	ORPHA:3474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000233	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000343	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000490	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000924	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001156	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001249	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001263	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001999	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0004689	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0008947	ORPHA:464288	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000028	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000212	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000316	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000457	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000463	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000470	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000486	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000964	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001250	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001256	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001328	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001513	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0010864	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0011220	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0012368	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0012443	ORPHA:464288	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000076	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000089	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000252	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000278	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000384	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000407	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000589	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000592	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000620	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000818	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0000852	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0001601	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0002079	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0002342	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0003065	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0007074	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0010535	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0011968	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464288	Short stature-brachydactyly-obesity-global developmental delay syndrome		HP:0031938	ORPHA:464288	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000938	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000974	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000978	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001373	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001382	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001582	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001760	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001763	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001765	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001822	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0031158	ORPHA:536532	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001537	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001634	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001999	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002827	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002933	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0004976	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0007457	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0025509	ORPHA:536532	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000023	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000028	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000189	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000218	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000347	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000400	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000465	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000483	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000486	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000545	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000692	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000704	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000767	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000819	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0000960	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001097	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001166	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001252	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001263	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001270	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001488	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001596	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001698	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001780	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0001852	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002155	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002616	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002619	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002751	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002808	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0002943	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0003042	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0003834	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0003994	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0006243	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0006439	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0006480	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0008138	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0009938	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0010810	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0010829	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0025232	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0100546	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536532	Classical-like Ehlers-Danlos syndrome type 2		HP:0100658	ORPHA:536532	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000076	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000085	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000218	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000233	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000238	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000252	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000286	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000316	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000319	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000347	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000348	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000384	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000486	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000506	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000582	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000664	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0000750	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0001252	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0001263	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0001274	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0001510	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0001671	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0002007	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0002069	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0002119	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0002263	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0002566	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0002650	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0004322	ORPHA:238769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0004422	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0005487	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0007766	ORPHA:238769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238769	1q44 microdeletion syndrome		HP:0010864	ORPHA:238769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0025637	ORPHA:284388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0030907	ORPHA:284388	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002076	ORPHA:284388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002331	ORPHA:284388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0410263	ORPHA:284388	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0000613	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0000622	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0001289	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0001342	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0001892	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002013	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002138	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002140	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002183	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002326	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002352	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0004302	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0004944	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0009145	ORPHA:284388	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0001250	ORPHA:284388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0002181	ORPHA:284388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0012158	ORPHA:284388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0030746	ORPHA:284388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284388	Reversible cerebral vasoconstriction syndrome		HP:0100309	ORPHA:284388	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000519	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001250	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001508	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002342	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002521	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002910	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0008947	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0010864	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0012758	ORPHA:86309	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000252	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000483	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000486	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000510	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000577	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000639	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000648	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000662	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000717	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000718	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000750	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000939	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000998	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001072	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001166	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001265	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001276	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001317	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001321	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001371	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001657	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001903	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001976	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002079	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002089	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002120	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002123	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002170	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002240	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002283	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002650	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0003186	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0003429	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0004855	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0008936	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0009125	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0010781	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0010845	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0011097	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0011153	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0011968	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0012050	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0012385	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0012512	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0025534	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0030084	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0030213	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0200134	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0410263	ORPHA:86309	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0000365	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001251	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001337	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001344	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001558	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0001989	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002304	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002401	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0002540	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0012168	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:86309	DPAGT1-CDG		HP:0012172	ORPHA:86309	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0000508	ORPHA:230800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0000651	ORPHA:230800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0001324	ORPHA:230800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0002015	ORPHA:230800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0002019	ORPHA:230800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0002094	ORPHA:230800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0002747	ORPHA:230800	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0003470	ORPHA:230800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0006597	ORPHA:230800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0006824	ORPHA:230800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0011499	ORPHA:230800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:230800	Toxin-mediated infectious botulism		HP:0100021	ORPHA:230800	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0100661	ORPHA:221091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0000716	ORPHA:221091	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0012199	ORPHA:221091	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0012533	ORPHA:221091	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0000183	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0000740	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0002465	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0003401	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0003474	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0004948	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0011968	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0200025	ORPHA:221091	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0001293	ORPHA:221091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0002664	ORPHA:221091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0007305	ORPHA:221091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0011096	ORPHA:221091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221091	Trigeminal neuralgia		HP:0200026	ORPHA:221091	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000008	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000022	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000028	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000046	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000047	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000048	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000062	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000130	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000144	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0000147	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0008736	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0010459	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0012856	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2138	46,XX ovotesticular difference of sex development		HP:0100779	ORPHA:2138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0003237	ORPHA:2137	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0010702	ORPHA:2137	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0002910	ORPHA:2137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0003262	ORPHA:2137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0003453	ORPHA:2137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0003493	ORPHA:2137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0030908	ORPHA:2137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0030909	ORPHA:2137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0031925	ORPHA:2137	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0000716	ORPHA:2137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0002027	ORPHA:2137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0002829	ORPHA:2137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0012432	ORPHA:2137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0012522	ORPHA:2137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0032469	ORPHA:2137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0000099	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0000739	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0000952	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0001045	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0001369	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0001394	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0001541	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0001744	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0002037	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0002239	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0003573	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0006555	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0030991	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0100279	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0100646	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0200119	ORPHA:2137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0001402	ORPHA:2137	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0004787	ORPHA:2137	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2137	Autoimmune hepatitis		HP:0006562	ORPHA:2137	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000316	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000369	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000431	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000684	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001004	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001249	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001530	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001888	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001999	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0002024	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0004313	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0005280	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0006482	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000377	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0009804	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0011069	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0012368	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0100764	ORPHA:2136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000212	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000286	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000337	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000501	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000774	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001055	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001250	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001541	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001744	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0002205	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0002716	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0011830	ORPHA:2136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000085	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000086	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000160	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000278	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000322	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0000405	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001302	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001363	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001698	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001760	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0001789	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0002021	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0002093	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0002215	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0002901	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0006101	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0006521	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0010310	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0100026	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0100490	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2136	Hennekam syndrome		HP:0100835	ORPHA:2136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0100747	ORPHA:295047	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0010165	ORPHA:295047	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0001783	ORPHA:295047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0008082	ORPHA:295047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0008108	ORPHA:295047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0008371	ORPHA:295047	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0001770	ORPHA:295047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0005830	ORPHA:295047	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0000023	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0000047	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0001397	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0001629	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0001631	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0001829	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0002650	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0008551	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295047	Macrodactyly of toes		HP:0012032	ORPHA:295047	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000179	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000218	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000325	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000648	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000989	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001000	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001249	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001252	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001284	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001508	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0002090	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0002093	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0002119	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0002615	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0002650	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0004322	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0008551	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0011344	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0012378	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0100559	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0200034	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000252	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000270	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000336	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000347	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000365	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000405	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000431	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000445	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000520	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000582	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000737	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0000924	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001025	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001072	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001250	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0001482	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0002013	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0002027	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0003189	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0004209	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0007400	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0007440	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0010783	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0011675	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0012733	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0100326	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0100490	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0100495	ORPHA:2135	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0100585	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0100725	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2135	Cutaneous mastocytosis-deafness-microtia syndrome		HP:0200037	ORPHA:2135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0000093	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0000790	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0001871	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0001873	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0001919	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0001937	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0001939	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0045040	ORPHA:2134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0004431	ORPHA:2134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0005339	ORPHA:2134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0005356	ORPHA:2134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0005416	ORPHA:2134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2134	Atypical hemolytic uremic syndrome		HP:0040229	ORPHA:2134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0000716	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0000739	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0001293	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0030164	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0030766	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0030811	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0032148	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0200025	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:3000047	ORPHA:221098	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0000174	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0001250	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0001279	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0001605	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0001609	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0001662	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0001824	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0002315	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0002617	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0002664	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0002960	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0003319	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0004395	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0007099	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0011968	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0012534	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0032043	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0100008	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221098	Glossopharyngeal neuralgia		HP:0200136	ORPHA:221098	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0004840	ORPHA:2133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0010972	ORPHA:2133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0011902	ORPHA:2133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0020059	ORPHA:2133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0025066	ORPHA:2133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0032231	ORPHA:2133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0011905	ORPHA:2133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0001511	ORPHA:2133	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0001622	ORPHA:2133	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0001744	ORPHA:2133	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0004817	ORPHA:2133	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0005546	ORPHA:2133	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2133	Hemoglobin E disease		HP:0005268	ORPHA:2133	TAS		HP:0040284			C	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002579	ORPHA:2131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0011024	ORPHA:2131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0012194	ORPHA:2131	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000565	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000577	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000639	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000708	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000750	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000980	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001249	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001250	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001251	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001332	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001508	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002013	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002014	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002015	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002019	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002039	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002273	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0003270	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0011499	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0012332	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0012547	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0012758	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0031284	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0200136	ORPHA:2131	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000297	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000348	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000657	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000712	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000718	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0000975	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001252	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001260	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001266	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001284	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001337	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001347	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001944	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002063	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002069	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002072	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002098	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002104	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002133	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002263	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002315	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002344	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002483	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002714	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0002835	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0005135	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0007166	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0007256	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0011153	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0031546	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0031931	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0032649	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0045074	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0100710	ORPHA:2131	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0001638	ORPHA:2131	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood		HP:0011675	ORPHA:2131	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood	NOT	HP:0002353	ORPHA:2131	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2131	Alternating hemiplegia of childhood	NOT	HP:0410263	ORPHA:2131	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:71289	Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome		HP:0000407	ORPHA:71289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71289	Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome		HP:0001385	ORPHA:71289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71289	Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome		HP:0002974	ORPHA:71289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71289	Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome		HP:0004209	ORPHA:71289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71289	Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome		HP:0004859	ORPHA:71289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71289	Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome		HP:0006101	ORPHA:71289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000407	ORPHA:3463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000648	ORPHA:3463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000819	ORPHA:3463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000873	ORPHA:3463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001959	ORPHA:3463	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000010	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000079	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000112	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000639	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001250	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001251	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001260	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0008872	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0100016	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0100518	ORPHA:3463	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000026	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000135	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000501	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000602	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000708	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000726	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000738	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0000823	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001249	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001387	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001638	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0001903	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002019	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002024	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002093	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002120	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002239	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002360	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002376	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002592	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0002871	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0003198	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0009830	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3463	Wolfram syndrome		HP:0012332	ORPHA:3463	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000013	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000054	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000135	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000411	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000821	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000823	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000824	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000831	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000842	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000938	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0001256	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0001260	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0001266	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0001268	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0001332	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0001510	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0001596	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0002750	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0003077	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0005135	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0008209	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0008214	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0008619	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0008669	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0008697	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0008734	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0010464	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0040171	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0100840	ORPHA:3464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000325	ORPHA:3464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000448	ORPHA:3464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000674	ORPHA:3464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000709	ORPHA:3464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0000738	ORPHA:3464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3464	Woodhouse-Sakati syndrome		HP:0040189	ORPHA:3464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0001291	ORPHA:3465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0002167	ORPHA:3465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0000183	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0001328	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0001347	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0001618	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0002015	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0002020	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0002205	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0002307	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0002445	ORPHA:3465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0033683	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0040262	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0100543	ORPHA:3465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0000252	ORPHA:3465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0000407	ORPHA:3465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0001250	ORPHA:3465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3465	Worster-Drought syndrome		HP:0007018	ORPHA:3465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0003537	ORPHA:3467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0011935	ORPHA:3467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0000791	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0000804	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0002932	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0003534	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0003643	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0010933	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0010934	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0011814	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0020074	ORPHA:3467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0000010	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0000126	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0000790	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0001370	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0001919	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0003040	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0003198	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0004396	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0012432	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0030157	ORPHA:3467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3467	Hereditary xanthinuria		HP:0001997	ORPHA:3467	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0000154	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0000311	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0000358	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0000414	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0000823	ORPHA:2139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0001250	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0001263	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0001513	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0002002	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2139	Hernández-Aguirre Negrete syndrome		HP:0002353	ORPHA:2139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0000160	ORPHA:3469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0000252	ORPHA:3469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0000568	ORPHA:3469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0000600	ORPHA:3469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0000811	ORPHA:3469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0002023	ORPHA:3469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0002818	ORPHA:3469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0005288	ORPHA:3469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0000601	ORPHA:3469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0001561	ORPHA:3469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0001629	ORPHA:3469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3469	XK aprosencephaly syndrome		HP:0001631	ORPHA:3469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0100746	ORPHA:295044	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0004276	ORPHA:295044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0005922	ORPHA:295044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0100774	ORPHA:295044	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0006101	ORPHA:295044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0010493	ORPHA:295044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0012185	ORPHA:295044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:295044	Macrodactyly of fingers		HP:0012186	ORPHA:295044	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001371	ORPHA:536516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001382	ORPHA:536516	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001270	ORPHA:536516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0003324	ORPHA:536516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0003557	ORPHA:536516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0025335	ORPHA:536516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0031936	ORPHA:536516	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0000347	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0000545	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0000592	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0000767	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0000974	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0000977	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0000980	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001058	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001181	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001182	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001252	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001284	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001319	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001508	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001601	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001762	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0001763	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0002650	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0002705	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0002751	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0002803	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0002808	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0002828	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0002987	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0003044	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0003199	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0003307	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0003546	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0003701	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0005879	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0005988	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0006380	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0006466	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0008180	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0008366	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0008780	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0009473	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0010499	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0010862	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0030051	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0030319	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536516	Myopathic Ehlers-Danlos syndrome		HP:0032152	ORPHA:536516	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000154	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000219	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000273	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000322	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000337	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000455	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000484	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000486	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000752	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0001263	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002121	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002213	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002465	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002500	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0008947	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0010864	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0012448	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0100807	ORPHA:363686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000047	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000218	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000286	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000316	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000347	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000483	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000490	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000582	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000609	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000629	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000637	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000729	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000742	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000744	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0000748	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0001382	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0001511	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0001566	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002007	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002061	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002360	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0002546	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0005280	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0008770	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0009836	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0010511	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0011968	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0012450	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0045025	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363686	Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome		HP:0100033	ORPHA:363686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0000488	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0001138	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002069	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002151	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002180	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002283	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002311	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002416	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002490	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002579	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0002922	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0003739	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0003808	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0011344	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0011451	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0011923	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0011924	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0012332	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0012448	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0030884	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0040078	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478029	Combined oxidative phosphorylation defect type 29		HP:0100275	ORPHA:478029	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000028	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000219	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000336	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000347	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000455	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000490	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000574	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000712	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000771	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001182	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001249	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001263	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001761	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001763	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001773	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001956	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001999	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0002465	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0004322	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0008551	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0010620	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0200055	ORPHA:3459	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0000044	ORPHA:3459	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001250	ORPHA:3459	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome		HP:0001328	ORPHA:3459	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome	NOT	HP:0000518	ORPHA:3459	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome	NOT	HP:0000540	ORPHA:3459	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3459	Wilson-Turner syndrome	NOT	HP:0009909	ORPHA:3459	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0001824	ORPHA:2126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0002664	ORPHA:2126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0010787	ORPHA:2126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0012378	ORPHA:2126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0031459	ORPHA:2126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0100527	ORPHA:2126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0000016	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0000290	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0000651	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0001943	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0001945	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0001988	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0002019	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0002585	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0002896	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0003419	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0004375	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0004912	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0007185	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0008775	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0010784	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0012125	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0030166	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0030795	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0031501	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0040216	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0045026	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0100526	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2126	Solitary fibrous tumor		HP:0100650	ORPHA:2126	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0002999	ORPHA:295036	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0001288	ORPHA:295036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0002829	ORPHA:295036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0002857	ORPHA:295036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0003066	ORPHA:295036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0003326	ORPHA:295036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0006380	ORPHA:295036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:295036	Congenital patella dislocation		HP:0009787	ORPHA:295036	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0000083	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0000142	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0000929	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001541	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001561	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001608	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001622	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001643	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001789	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001873	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001903	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001928	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0001939	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0002240	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0003072	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0007461	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0008678	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0030680	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2123	Multifocal infantile hemangioma with extracutenous involvement		HP:0100761	ORPHA:2123	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0005520	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0011900	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0012531	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0025474	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0030350	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0033106	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0000975	ORPHA:2122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0000967	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0000969	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0000979	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0001004	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0001873	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0001937	ORPHA:2122	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2122	Kaposiform hemangioendothelioma		HP:0000998	ORPHA:2122	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0000238	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0000520	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0000554	ORPHA:3452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0000716	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0000821	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0000855	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001250	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001251	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001324	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001336	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001369	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001658	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001701	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001744	ORPHA:3452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001903	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001945	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0001959	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002014	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002024	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002027	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002039	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002093	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002102	ORPHA:3452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002239	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002240	ORPHA:3452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002360	ORPHA:3452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002376	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002383	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002516	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002615	ORPHA:3452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002829	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0002902	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0003326	ORPHA:3452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0004326	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0006824	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0007256	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0007440	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0009830	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0010741	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0012378	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0012735	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0012819	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0100614	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0100639	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0100721	ORPHA:3452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0100749	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3452	Whipple disease		HP:0100829	ORPHA:3452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000829	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0002728	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0002960	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0003118	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0004319	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0008207	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0008221	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0100530	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0100659	ORPHA:3453	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000518	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000613	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000953	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000968	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0001096	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0006297	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0007759	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0008209	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0034055	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0034071	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0100502	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0100651	ORPHA:3453	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000123	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000135	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000554	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000648	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0000872	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0001045	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0001053	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0001596	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0001746	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0002024	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0002582	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0006515	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0007663	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0008404	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0008720	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0012115	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3453	Autoimmune polyendocrinopathy type 1		HP:0012804	ORPHA:3453	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0000486	ORPHA:3454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0000496	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0000508	ORPHA:3454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0000657	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0001256	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0001263	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0001376	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0002167	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0002650	ORPHA:3454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0002808	ORPHA:3454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0003693	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0004209	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0005745	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3454	Wieacker-Wolff syndrome		HP:0100022	ORPHA:3454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000160	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000219	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000272	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000278	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000292	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000307	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000316	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000322	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000325	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000337	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000358	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000444	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000490	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000582	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000621	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000695	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001043	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001511	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001533	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002007	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002209	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002714	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000444	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0003758	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0004322	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0004482	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0004492	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0005328	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0008846	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0009059	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0100578	ORPHA:3455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000028	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000044	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000126	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000164	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000238	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000267	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000364	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000369	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000403	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000518	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000540	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000545	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000598	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000664	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000668	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000824	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000870	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000938	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000956	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000963	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001007	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001257	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001263	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001276	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001289	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001382	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001385	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001397	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001508	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001510	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001581	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001945	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002078	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002155	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002342	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002415	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002509	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002684	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002751	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0003097	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0003326	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0003429	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0003712	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0005792	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0006470	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0006480	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0007957	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0008070	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0008386	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0008476	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0009003	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0010511	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0010648	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0011410	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0011819	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0011968	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0012811	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0100490	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0100678	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0100769	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0100807	ORPHA:3455	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000010	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000076	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000387	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000463	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000580	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000639	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000648	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000771	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000946	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001250	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001251	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001274	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001321	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001337	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001601	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0001642	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002126	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0002345	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0003413	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0004691	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0007099	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0008469	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0008479	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0010994	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0030265	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0100581	ORPHA:3455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000047	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000592	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0000836	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0005164	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0005978	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0007766	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0025134	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0030001	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0030088	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3455	Wiedemann-Rautenstrauch syndrome		HP:0045017	ORPHA:3455	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0000470	ORPHA:3456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0002949	ORPHA:3456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0006897	ORPHA:3456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0008527	ORPHA:3456	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0000324	ORPHA:3456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0000465	ORPHA:3456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0000538	ORPHA:3456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0001132	ORPHA:3456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0002162	ORPHA:3456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0002435	ORPHA:3456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3456	Wildervanck syndrome		HP:0010628	ORPHA:3456	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0002500	ORPHA:447788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0002060	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000238	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0011450	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0001250	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0025315	ORPHA:447788	TAS		HP:0040283			M	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0002180	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0100021	ORPHA:447788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0010794	ORPHA:447788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0001249	ORPHA:447788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000252	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0007009	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000486	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000539	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000639	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0012796	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000543	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0001141	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0025405	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0007772	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0001123	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000736	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0007018	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000729	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0002312	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000496	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0001622	ORPHA:447788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0002140	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0001998	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0002170	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0032046	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0001287	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0002383	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0012443	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0410263	ORPHA:447788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0030800	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0500049	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000609	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000648	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000641	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447788	Cerebral visual impairment		HP:0000657	ORPHA:447788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0001528	ORPHA:2128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0001555	ORPHA:2128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0002650	ORPHA:2128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0000164	ORPHA:2128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0000324	ORPHA:2128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0001256	ORPHA:2128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0000023	ORPHA:2128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0000028	ORPHA:2128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0002475	ORPHA:2128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0002667	ORPHA:2128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0007328	ORPHA:2128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2128	Isolated hemihyperplasia		HP:0030680	ORPHA:2128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0001824	ORPHA:103910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0002014	ORPHA:103910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0002243	ORPHA:103910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0003073	ORPHA:103910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0011012	ORPHA:103910	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0000969	ORPHA:103910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0001944	ORPHA:103910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0002573	ORPHA:103910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0003270	ORPHA:103910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103910	Congenital enterocyte heparan sulfate deficiency		HP:0010876	ORPHA:103910	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0000473	ORPHA:71272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0002020	ORPHA:71272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0002457	ORPHA:71272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0002533	ORPHA:71272	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0001903	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0002036	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0002248	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0004637	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0011968	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0012547	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0100633	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0410019	ORPHA:71272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71272	Sandifer syndrome		HP:0002572	ORPHA:71272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0000093	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0000716	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0000790	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0001920	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0002619	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0003419	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0011934	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0012871	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0030157	ORPHA:71273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0001903	ORPHA:71273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0002907	ORPHA:71273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0012378	ORPHA:71273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0034267	ORPHA:71273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0100518	ORPHA:71273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0100677	ORPHA:71273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0000789	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0001278	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0001279	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0001649	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0001824	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0002018	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0002027	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0012332	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0030016	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71273	Renal nutcracker syndrome		HP:0100607	ORPHA:71273	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0000539	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0000551	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0000613	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0007803	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0012043	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0030465	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0030584	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0030620	ORPHA:49382	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0000540	ORPHA:49382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0000545	ORPHA:49382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0000603	ORPHA:49382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0007663	ORPHA:49382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0007750	ORPHA:49382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0030825	ORPHA:49382	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0001103	ORPHA:49382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0007695	ORPHA:49382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0007814	ORPHA:49382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0007843	ORPHA:49382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0025549	ORPHA:49382	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:49382	Achromatopsia		HP:0007722	ORPHA:49382	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001273	ORPHA:221074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0004395	ORPHA:221074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0030955	ORPHA:221074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0100503	ORPHA:221074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001259	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001260	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001288	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002066	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002315	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002354	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002509	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0007185	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0007305	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0100543	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0100851	ORPHA:221074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000020	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000504	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000602	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000639	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000651	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000708	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000709	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000716	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000718	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000726	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000741	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0000746	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001250	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001251	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001262	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001269	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001289	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002013	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002063	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002134	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002186	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002273	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002300	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002321	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002367	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002381	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002476	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0002922	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0007256	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0010522	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0010526	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0010628	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0030784	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0031258	ORPHA:221074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221074	Marchiafava-Bignami disease		HP:0001945	ORPHA:221074	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0005213	ORPHA:103918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0005236	ORPHA:103918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0410019	ORPHA:103918	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0002018	ORPHA:103918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0008205	ORPHA:103918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0030992	ORPHA:103918	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0000952	ORPHA:103918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0001824	ORPHA:103918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0002013	ORPHA:103918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0004395	ORPHA:103918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0006725	ORPHA:103918	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103918	Tropical pancreatitis		HP:0009800	ORPHA:103918	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000712	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000738	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000739	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000992	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001251	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001252	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001347	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0002076	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0002353	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0008353	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0012086	ORPHA:2116	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000486	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000504	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000613	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000639	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000988	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001337	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0002024	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:6000130	ORPHA:2116	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000206	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000230	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0000709	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001053	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001249	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001250	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0001263	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0002383	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0004322	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0007400	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2116	Hartnup disease		HP:0008066	ORPHA:2116	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3448	Weaver-Williams syndrome		HP:0000160	ORPHA:3448	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3448	Weaver-Williams syndrome		HP:0000175	ORPHA:3448	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3448	Weaver-Williams syndrome		HP:0000252	ORPHA:3448	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3448	Weaver-Williams syndrome		HP:0000411	ORPHA:3448	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3448	Weaver-Williams syndrome		HP:0002342	ORPHA:3448	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3448	Weaver-Williams syndrome		HP:0004325	ORPHA:3448	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3448	Weaver-Williams syndrome		HP:0010864	ORPHA:3448	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000003	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000028	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000047	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000160	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000218	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000252	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000275	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000276	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000307	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000411	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000518	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000601	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0000689	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0001053	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0001166	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0001249	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0001250	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0001508	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0001511	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0002120	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0002644	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0002650	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0002808	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0003043	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0003189	ORPHA:2115	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2115	Harrod syndrome		HP:0001382	ORPHA:2115	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0000501	ORPHA:3449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001156	ORPHA:3449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0004322	ORPHA:3449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0009778	ORPHA:3449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0011003	ORPHA:3449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0030961	ORPHA:3449	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001072	ORPHA:3449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001083	ORPHA:3449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001376	ORPHA:3449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0030680	ORPHA:3449	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0000518	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0000572	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001256	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001387	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001629	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001642	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001643	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001650	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0001653	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0002750	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3449	Weill-Marchesani syndrome		HP:0005184	ORPHA:3449	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0001385	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0002650	ORPHA:2114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0002758	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0002808	ORPHA:2114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0002812	ORPHA:2114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0004348	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0005930	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0006429	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0009107	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0010574	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2114	Hip dysplasia, Beukes type		HP:0011849	ORPHA:2114	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103909	Trehalase deficiency		HP:0012379	ORPHA:103909	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103909	Trehalase deficiency		HP:0002013	ORPHA:103909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103909	Trehalase deficiency		HP:0002014	ORPHA:103909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103909	Trehalase deficiency		HP:0002024	ORPHA:103909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103909	Trehalase deficiency		HP:0002027	ORPHA:103909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103909	Trehalase deficiency		HP:0003270	ORPHA:103909	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2111	Cystic hamartoma of lung and kidney		HP:0000003	ORPHA:2111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2111	Cystic hamartoma of lung and kidney		HP:0000822	ORPHA:2111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2111	Cystic hamartoma of lung and kidney		HP:0002093	ORPHA:2111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2111	Cystic hamartoma of lung and kidney		HP:0002205	ORPHA:2111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2111	Cystic hamartoma of lung and kidney		HP:0002206	ORPHA:2111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2110	Hallux varus-preaxial polysyndactyly syndrome		HP:0001852	ORPHA:2110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2110	Hallux varus-preaxial polysyndactyly syndrome		HP:0004209	ORPHA:2110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0000183	ORPHA:412217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0001260	ORPHA:412217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0001288	ORPHA:412217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0001618	ORPHA:412217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0002015	ORPHA:412217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0005216	ORPHA:412217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0007325	ORPHA:412217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0000158	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0001250	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0001272	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0002059	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0002317	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0002425	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0007327	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0007885	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0008777	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0012048	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0012087	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0012088	ORPHA:412217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0000212	ORPHA:412217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0000739	ORPHA:412217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0001263	ORPHA:412217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0001336	ORPHA:412217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412217	Dystonia-aphonia syndrome		HP:0100543	ORPHA:412217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000365	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000426	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000664	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0001000	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0001053	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0001100	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0001999	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0002216	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0005599	ORPHA:3440	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000407	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000430	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000431	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000478	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000506	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000534	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0002211	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0008527	ORPHA:3440	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000202	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000508	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0000635	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0002227	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0002251	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0002321	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0002414	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0002475	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0005214	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0008568	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0009830	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0011024	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0012385	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0034391	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3440	Waardenburg syndrome		HP:0100811	ORPHA:3440	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0000322	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0000407	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0000426	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0000684	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0000703	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0000926	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0000939	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0001256	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0001999	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0004322	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71267	Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome		HP:0010579	ORPHA:71267	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002187	ORPHA:468699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0006829	ORPHA:468699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0008277	ORPHA:468699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0012301	ORPHA:468699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0012736	ORPHA:468699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0032098	ORPHA:468699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0000486	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0001250	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0001272	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0001531	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002120	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002421	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002540	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0004322	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0025405	ORPHA:468699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0000365	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0000369	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0000483	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0000540	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0000639	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0000938	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0001332	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0001347	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0001363	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0001392	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002119	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002465	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002490	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002521	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002719	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002882	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002928	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0002987	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0006380	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0006558	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0008314	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0008347	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0008873	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0009826	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0010621	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468699	SLC39A8-CDG		HP:0012368	ORPHA:468699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0011274	ORPHA:319552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0032283	ORPHA:319552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0011117	ORPHA:319552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0005661	ORPHA:319552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0005401	ORPHA:319552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0007408	ORPHA:319552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0002840	ORPHA:319552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0002090	ORPHA:319552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0002721	ORPHA:319552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0020087	ORPHA:319552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0200029	ORPHA:319552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0002742	ORPHA:319552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0032256	ORPHA:319552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0032249	ORPHA:319552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319552	Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency		HP:0020105	ORPHA:319552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0001250	ORPHA:95232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0006891	ORPHA:95232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0012469	ORPHA:95232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0000253	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0001273	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0001302	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002079	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002119	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002389	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002421	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002445	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002463	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0007772	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0008936	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0010850	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0010864	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0011968	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0012520	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0012758	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0020191	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0025336	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0031882	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0032398	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0200134	ORPHA:95232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0001256	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0001319	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0001561	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002123	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002179	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002187	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002376	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002384	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002521	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0003265	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0007270	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0010818	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0010819	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0011153	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0011201	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0011951	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0020189	ORPHA:95232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0001320	ORPHA:95232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002478	ORPHA:95232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:95232	Lissencephaly due to LIS1 mutation		HP:0002650	ORPHA:95232	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002064	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002174	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002344	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002464	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002493	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002505	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0003487	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0007083	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0007178	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0007240	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0007350	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0001761	ORPHA:447757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0000519	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0000726	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0001252	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002020	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0002987	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0003438	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0003477	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0004373	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447757	Autosomal dominant spastic paraplegia type 9B		HP:0006827	ORPHA:447757	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0000519	ORPHA:2119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0000600	ORPHA:2119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0000615	ORPHA:2119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0001334	ORPHA:2119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0001561	ORPHA:2119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0001622	ORPHA:2119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0001638	ORPHA:2119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0001706	ORPHA:2119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0002093	ORPHA:2119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0008046	ORPHA:2119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0011675	ORPHA:2119	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2119	HEC syndrome		HP:0100673	ORPHA:2119	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0000821	ORPHA:2118	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0001252	ORPHA:2118	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0001508	ORPHA:2118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0001942	ORPHA:2118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0002213	ORPHA:2118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0003161	ORPHA:2118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0003607	ORPHA:2118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0008070	ORPHA:2118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2118	Hawkinsinuria		HP:0010917	ORPHA:2118	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000098	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000256	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000278	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000316	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000337	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000343	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000347	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000358	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000400	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000944	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001231	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001249	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001257	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001263	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001276	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001582	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001609	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001800	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001814	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001816	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0005616	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0010300	ORPHA:3447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000023	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000311	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001176	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001387	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001769	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0002002	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0002213	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0008872	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0011304	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0100490	ORPHA:3447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000028	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0000494	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001761	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001762	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001852	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0002650	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0001382	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0006101	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0008736	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3447	Weaver syndrome		HP:0030680	ORPHA:3447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0000175	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0000316	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0000358	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0000494	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0000506	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0000508	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0000568	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0001171	ORPHA:2117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0001363	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0001511	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0002084	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0002093	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0005280	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0006501	ORPHA:2117	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0006870	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0007370	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2117	Hartsfield syndrome		HP:0100335	ORPHA:2117	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0100515	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002064	ORPHA:447753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002395	ORPHA:447753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0007350	ORPHA:447753	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0001761	ORPHA:447753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0003487	ORPHA:447753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0006895	ORPHA:447753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0007256	ORPHA:447753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0010832	ORPHA:447753	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0000012	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0000020	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0000407	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0000519	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0000666	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0000709	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0000726	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0001250	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0001317	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0001324	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0001337	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0001653	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002166	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002172	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002280	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002354	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002425	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002464	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002500	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0002527	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0003394	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0003419	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0007371	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0011397	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447753	Autosomal dominant spastic paraplegia type 9A		HP:0012514	ORPHA:447753	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0001257	ORPHA:447760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002395	ORPHA:447760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0003487	ORPHA:447760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0007350	ORPHA:447760	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0001260	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0001270	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0001324	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0001510	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002064	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002174	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002445	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0031064	ORPHA:447760	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0000016	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0000252	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0000750	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0001263	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0001999	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002120	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002371	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002476	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002518	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0002751	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0003202	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0003438	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0004322	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0006938	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0007371	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0030051	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447760	Autosomal recessive spastic paraplegia type 9B		HP:0100515	ORPHA:447760	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000400	ORPHA:589905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0001249	ORPHA:589905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0012758	ORPHA:589905	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000233	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000316	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000343	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000348	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000455	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000463	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000539	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000540	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000664	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000957	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0001182	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0001252	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0004209	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0004324	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0007018	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0008872	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0012378	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0100710	ORPHA:589905	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000028	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000286	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000403	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000486	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000508	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0000582	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0001250	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0001288	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0001319	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0002019	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0002020	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0002360	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0002378	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0002761	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0002788	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0004691	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:589905	PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome		HP:0007874	ORPHA:589905	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002500	ORPHA:247691	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0008046	ORPHA:247691	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0030880	ORPHA:247691	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000093	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000096	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000112	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000708	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000822	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0001895	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0001897	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002076	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0003155	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0003259	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0006707	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0008223	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0011954	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0030948	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0100543	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0410263	ORPHA:247691	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000501	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000709	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000716	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000737	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000739	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000741	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0001009	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0001123	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0001269	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0001638	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002077	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002083	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002090	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002197	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002239	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002344	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002354	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002381	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0002514	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0011163	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0012377	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0030319	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0030666	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0031606	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0040049	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0040328	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0040331	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0100806	ORPHA:247691	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0000988	ORPHA:247691	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0005743	ORPHA:247691	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247691	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations		HP:0200030	ORPHA:247691	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0002028	ORPHA:103907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0003270	ORPHA:103907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0012379	ORPHA:103907	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0002024	ORPHA:103907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0002027	ORPHA:103907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0025129	ORPHA:103907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0025130	ORPHA:103907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0410281	ORPHA:103907	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0002013	ORPHA:103907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:103907	Chronic diarrhea due to glucoamylase deficiency		HP:0002018	ORPHA:103907	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000499	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000534	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0001045	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0001053	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0002209	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0002216	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0002290	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0002315	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0012229	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0100543	ORPHA:3437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000360	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000407	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000505	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000518	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000541	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000554	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000622	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0001094	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0004322	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0007787	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0007906	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0020120	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0030953	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0031179	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0040030	ORPHA:3437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000501	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0000613	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0001596	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0001945	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0002018	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0002321	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0002381	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0009926	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0011484	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0025341	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:0100809	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3437	Vogt-Koyanagi-Harada disease		HP:6000710	ORPHA:3437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0000272	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0000293	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0000444	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0000457	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0000506	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0000768	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0002002	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0002007	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0002857	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0001382	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2104	Dysmorphism-pectus carinatum-joint laxity syndrome		HP:0010804	ORPHA:2104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0001873	ORPHA:3439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0002085	ORPHA:3439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0006496	ORPHA:3439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0009813	ORPHA:3439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000750	ORPHA:3439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0001263	ORPHA:3439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0001328	ORPHA:3439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0006501	ORPHA:3439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0007370	ORPHA:3439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000028	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000034	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000044	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000047	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000054	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000062	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000079	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000453	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0000692	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0001250	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0001627	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0002650	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0002808	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3439	Von Voss-Cherstvoy syndrome		HP:0100702	ORPHA:3439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000164	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000311	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000470	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000496	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000592	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000750	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000958	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0000964	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0001250	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0001252	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0001263	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0001315	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0001338	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0004097	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2101	Grubben-de Cock-Borghgraef syndrome		HP:0200055	ORPHA:2101	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000164	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000233	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000239	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000293	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000316	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000322	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000337	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000348	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000365	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000369	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000470	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000486	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000508	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000527	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000664	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000717	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000733	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0000750	ORPHA:238750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001250	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001252	ORPHA:238750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001263	ORPHA:238750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001274	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001321	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001337	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001510	ORPHA:238750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001511	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001770	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0001773	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002007	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002119	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002230	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002360	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002650	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002714	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002808	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0002983	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0004279	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0005280	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0010864	ORPHA:238750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0011344	ORPHA:238750	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0100716	ORPHA:238750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238750	4q21 microdeletion syndrome		HP:0200055	ORPHA:238750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0000252	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0000268	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0000272	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0000369	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0000400	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0002187	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0002362	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0002705	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0002751	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0003199	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0004322	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0005469	ORPHA:3433	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0000494	ORPHA:3433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0000518	ORPHA:3433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0003413	ORPHA:3433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0005620	ORPHA:3433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0010055	ORPHA:3433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0011304	ORPHA:3433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3433	Microcephaly-brachydactyly-kyphoscoliosis syndrome		HP:0012811	ORPHA:3433	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000164	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000248	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000444	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000519	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000568	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000773	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000896	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0001596	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0002007	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0002231	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0003508	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0004334	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0004349	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0008070	ORPHA:2108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000157	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000160	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000162	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000235	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000272	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000347	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000430	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000505	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000506	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000653	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000695	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0002705	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0002757	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0010719	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0011069	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0045075	ORPHA:2108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000028	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000252	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000453	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000486	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000501	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000545	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000554	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000639	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000821	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0000929	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0001249	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0001321	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0001635	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0001773	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0002093	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0002779	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0003363	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0004209	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0030680	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2108	Hallermann-Streiff syndrome		HP:0200055	ORPHA:2108	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0000028	ORPHA:3434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0000161	ORPHA:3434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0000202	ORPHA:3434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0000252	ORPHA:3434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0000303	ORPHA:3434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0000505	ORPHA:3434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0000568	ORPHA:3434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0001199	ORPHA:3434	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0001249	ORPHA:3434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0001629	ORPHA:3434	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3434	MMEP syndrome		HP:0001839	ORPHA:3434	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0001878	ORPHA:71275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0001923	ORPHA:71275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0005502	ORPHA:71275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0020181	ORPHA:71275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0032366	ORPHA:71275	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0002904	ORPHA:71275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0004444	ORPHA:71275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0004446	ORPHA:71275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0025435	ORPHA:71275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0032231	ORPHA:71275	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0000952	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0001433	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0001511	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0001562	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0001649	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0002789	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0005268	ORPHA:71275	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0011273	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0012418	ORPHA:71275	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71275	Rh deficiency syndrome		HP:0001972	ORPHA:71275	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000154	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000252	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000286	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000316	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000431	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000448	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000463	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000682	ORPHA:2107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000684	ORPHA:2107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000926	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0000944	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0001156	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0001250	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0001344	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0001387	ORPHA:2107	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0001508	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0002017	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0002208	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0002217	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0002650	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0002714	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0002750	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0004322	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0005930	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0009826	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0010864	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0011344	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0012471	ORPHA:2107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2107	Hall-Riggs syndrome		HP:0100874	ORPHA:2107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71276	Silent sinus syndrome		HP:0000478	ORPHA:71276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71276	Silent sinus syndrome		HP:0000490	ORPHA:71276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71276	Silent sinus syndrome		HP:0000504	ORPHA:71276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0000253	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001250	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001251	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001257	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001263	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001298	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001332	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001877	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0002133	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0002353	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0011972	ORPHA:71277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0000750	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0000961	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001249	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001254	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001260	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001266	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001269	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001276	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001289	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0002072	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0002315	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0003470	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0003552	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0007034	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0007308	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0007704	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0100660	ORPHA:71277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0000486	ORPHA:71277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0001336	ORPHA:71277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0002186	ORPHA:71277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0002360	ORPHA:71277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71277	Classic glucose transporter type 1 deficiency syndrome		HP:0002871	ORPHA:71277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001945	ORPHA:79139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002353	ORPHA:79139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002383	ORPHA:79139	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0000273	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0000298	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002013	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002039	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002069	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002315	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002396	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002516	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002922	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0003202	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0003326	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0003431	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0003444	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0003470	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0003496	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0004302	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0004372	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0007277	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0009053	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010549	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010702	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0011897	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0012229	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0012378	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0012692	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0025143	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0040272	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0200149	ORPHA:79139	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0000639	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0000708	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001259	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001266	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001276	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001287	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001332	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001336	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001337	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0001762	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002014	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002027	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002060	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002071	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002098	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002133	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002179	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002181	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002203	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002339	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002418	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002463	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002793	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002816	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002902	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0002987	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0003781	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0007361	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0007695	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0007941	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0008959	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010543	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010546	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010547	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010628	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010663	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010851	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0010864	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0011153	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0011182	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0011468	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0012195	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0012502	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0025145	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0025258	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0025387	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0030826	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0031218	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0045007	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0100543	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79139	Japanese encephalitis		HP:0100598	ORPHA:79139	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0001335	ORPHA:238722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0002312	ORPHA:238722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0002492	ORPHA:238722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0003388	ORPHA:238722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0007010	ORPHA:238722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0100022	ORPHA:238722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0001274	ORPHA:238722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0001328	ORPHA:238722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0003326	ORPHA:238722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0025101	ORPHA:238722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0000044	ORPHA:238722	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0001256	ORPHA:238722	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0002949	ORPHA:238722	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238722	Familial congenital mirror movements		HP:0100021	ORPHA:238722	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0002322	ORPHA:363654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0002396	ORPHA:363654	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0001257	ORPHA:363654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0002067	ORPHA:363654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0003487	ORPHA:363654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0006801	ORPHA:363654	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0000298	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0001250	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0002313	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0002506	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0006956	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0007082	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0011448	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363654	X-linked parkinsonism-spasticity syndrome		HP:0012407	ORPHA:363654	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000028	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000048	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000212	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000252	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000278	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000280	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000286	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000293	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000358	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000431	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000520	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000750	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0001263	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0001510	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0001773	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0002342	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0003196	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0004279	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0005280	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0005487	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0008551	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0009891	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0010804	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0011003	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0011825	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0012368	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0100539	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0100540	ORPHA:363659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000023	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000054	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000190	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000243	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000248	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000325	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000341	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000422	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000463	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000494	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000508	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000639	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000736	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000767	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000768	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0000960	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0001250	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0001377	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0004209	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0006191	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0008846	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0009894	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0010864	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0031008	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363659	20q11.2 microduplication syndrome		HP:0200005	ORPHA:363659	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001719	ORPHA:3426	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0000961	ORPHA:3426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0000160	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0000175	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0000176	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0000316	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001256	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001508	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001629	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001642	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001649	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0002789	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0004322	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0004383	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0005280	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0011968	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0030148	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0045025	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:3000022	ORPHA:3426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0000829	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001636	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001660	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0001680	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0002566	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0002901	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0004935	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0010515	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3426	Double outlet right ventricle		HP:0030853	ORPHA:3426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0011581	ORPHA:3427	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0001629	ORPHA:3427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0001643	ORPHA:3427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0033118	ORPHA:3427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0000961	ORPHA:3427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0001640	ORPHA:3427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0011662	ORPHA:3427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0011686	ORPHA:3427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0000028	ORPHA:3427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0000202	ORPHA:3427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0000316	ORPHA:3427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0001508	ORPHA:3427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0002789	ORPHA:3427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0031664	ORPHA:3427	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0004415	ORPHA:3427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0005182	ORPHA:3427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3427	Double outlet left ventricle		HP:0010882	ORPHA:3427	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0000028	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0000175	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0000347	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0000369	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0000413	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0000828	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0002644	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0002823	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0003312	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0005916	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0006703	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0008368	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0008551	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0009826	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0030680	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0100335	ORPHA:3429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0006101	ORPHA:3429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3429	Verloove Vanhorick-Brubakk syndrome		HP:0100542	ORPHA:3429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000153	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000234	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000263	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000286	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000316	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000457	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000470	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0000476	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0001156	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0001433	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0001538	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0002816	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0003026	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0003196	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0005257	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0005458	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0008551	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0009826	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221054	Acrocephalopolydactyly		HP:0012210	ORPHA:221054	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0030447	ORPHA:79140	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0000992	ORPHA:79140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0002730	ORPHA:79140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0005374	ORPHA:79140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0011356	ORPHA:79140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0025474	ORPHA:79140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0025475	ORPHA:79140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0200036	ORPHA:79140	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0002671	ORPHA:79140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0005526	ORPHA:79140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0006739	ORPHA:79140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0006775	ORPHA:79140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0100570	ORPHA:79140	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0012658	ORPHA:79140	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0030692	ORPHA:79140	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma		HP:0040095	ORPHA:79140	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79140	Cutaneous neuroendocrine carcinoma	NOT	HP:0012531	ORPHA:79140	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79141	Hereditary painful callosities		HP:0005588	ORPHA:79141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79141	Hereditary painful callosities		HP:0012531	ORPHA:79141	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0033555	ORPHA:163525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0000992	ORPHA:163525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0002923	ORPHA:163525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0003493	ORPHA:163525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0025526	ORPHA:163525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0025528	ORPHA:163525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0000962	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0003613	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0004334	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0007417	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0008066	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0020151	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0031540	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0031541	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0032235	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0033558	ORPHA:163525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0025300	ORPHA:163525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0100825	ORPHA:163525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:163525	Subacute cutaneous lupus erythematosus		HP:0200029	ORPHA:163525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0003565	ORPHA:411703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002110	ORPHA:411703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0012735	ORPHA:411703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0025406	ORPHA:411703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0031457	ORPHA:411703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0032016	ORPHA:411703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0001698	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0001824	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0001945	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002014	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002094	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002098	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002105	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002202	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002716	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0006510	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0030830	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0032130	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0032283	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0100749	ORPHA:411703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411703	Pulmonary non-tuberculous mycobacterial infection		HP:0002107	ORPHA:411703	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0001816	ORPHA:79144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0010793	ORPHA:79144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0030805	ORPHA:79144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0100797	ORPHA:79144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0100798	ORPHA:79144	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0001598	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0001792	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0005918	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0008401	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0009951	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0011313	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0030803	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0031282	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0040036	ORPHA:79144	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0001798	ORPHA:79144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0012203	ORPHA:79144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0012710	ORPHA:79144	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0000202	ORPHA:79144	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0001385	ORPHA:79144	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0002650	ORPHA:79144	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0004691	ORPHA:79144	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79144	Isolated congenital onychodysplasia		HP:0012296	ORPHA:79144	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0007456	ORPHA:79145	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0000464	ORPHA:79145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0000962	ORPHA:79145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0030052	ORPHA:79145	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0000989	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0001034	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0001155	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0001231	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0002046	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0012855	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0025473	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0030350	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0031293	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0031447	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0040154	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0045059	ORPHA:79145	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0001369	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0009123	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0010610	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0011354	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0020073	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0030442	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0031525	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0200037	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79145	Dowling-Degos disease		HP:0200040	ORPHA:79145	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis	NOT	HP:0001231	ORPHA:79147	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis	NOT	HP:0012622	ORPHA:79147	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0030350	ORPHA:79147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0040186	ORPHA:79147	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0005585	ORPHA:79147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0011123	ORPHA:79147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0011124	ORPHA:79147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0025164	ORPHA:79147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0031512	ORPHA:79147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0045059	ORPHA:79147	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0000377	ORPHA:79147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0000606	ORPHA:79147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0000989	ORPHA:79147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0001965	ORPHA:79147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0007473	ORPHA:79147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0012322	ORPHA:79147	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis		HP:0011830	ORPHA:79147	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis	NOT	HP:0000164	ORPHA:79147	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis	NOT	HP:0000819	ORPHA:79147	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79147	Familial reactive perforating collagenosis	NOT	HP:0001005	ORPHA:79147	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000164	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000275	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000276	ORPHA:3424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000286	ORPHA:3424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000316	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000324	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000431	ORPHA:3424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000474	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0000506	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0001172	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0001176	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0001212	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0001622	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0002705	ORPHA:3424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0002750	ORPHA:3424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0004209	ORPHA:3424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0004279	ORPHA:3424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3424	Velo-facial-skeletal syndrome		HP:0004322	ORPHA:3424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0000104	ORPHA:411709	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0000122	ORPHA:411709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0012300	ORPHA:411709	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0000083	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0000093	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0000822	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0001562	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0001629	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0001762	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0002009	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0002023	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0002089	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0008684	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0010476	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0010958	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:411709	Renal agenesis		HP:0012873	ORPHA:411709	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0000464	ORPHA:79148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0045059	ORPHA:79148	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0000271	ORPHA:79148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0025512	ORPHA:79148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0025527	ORPHA:79148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0025528	ORPHA:79148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0030350	ORPHA:79148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0200035	ORPHA:79148	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0000973	ORPHA:79148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0007473	ORPHA:79148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79148	Elastosis perforans serpiginosa		HP:0025092	ORPHA:79148	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79149	Dermochondrocorneal dystrophy		HP:0000924	ORPHA:79149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79149	Dermochondrocorneal dystrophy		HP:0000991	ORPHA:79149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79149	Dermochondrocorneal dystrophy		HP:0001131	ORPHA:79149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79149	Dermochondrocorneal dystrophy		HP:0001155	ORPHA:79149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79149	Dermochondrocorneal dystrophy		HP:0001176	ORPHA:79149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79149	Dermochondrocorneal dystrophy		HP:0001760	ORPHA:79149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79149	Dermochondrocorneal dystrophy		HP:0007663	ORPHA:79149	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0012735	ORPHA:79128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0000964	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0001217	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0001508	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0002091	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0002094	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0002960	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0005948	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0012378	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0012418	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0025179	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0030057	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0030828	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0030830	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0031691	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0032177	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0045051	ORPHA:79128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0000105	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0000988	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0001097	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0001370	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0001824	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0001945	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0002110	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0002240	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0002721	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0003549	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0011947	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0025178	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0025180	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0030880	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0030950	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0100721	ORPHA:79128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79128	Lymphoid interstitial pneumonia		HP:0002206	ORPHA:79128	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79129	Trichodysplasia-amelogenesis imperfecta syndrome		HP:0000705	ORPHA:79129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79129	Trichodysplasia-amelogenesis imperfecta syndrome		HP:0002293	ORPHA:79129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79129	Trichodysplasia-amelogenesis imperfecta syndrome		HP:0002552	ORPHA:79129	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0000982	ORPHA:34217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0001638	ORPHA:34217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0002224	ORPHA:34217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0002321	ORPHA:34217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0004751	ORPHA:34217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0010719	ORPHA:34217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0011675	ORPHA:34217	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0000204	ORPHA:34217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0000975	ORPHA:34217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0001635	ORPHA:34217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0002209	ORPHA:34217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0002212	ORPHA:34217	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0000956	ORPHA:34217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:34217	Naxos disease		HP:0001645	ORPHA:34217	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0100561	ORPHA:221061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0002858	ORPHA:221061	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0009588	ORPHA:221061	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0009592	ORPHA:221061	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0010512	ORPHA:221061	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0033522	ORPHA:221061	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0001250	ORPHA:221061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0001342	ORPHA:221061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0002315	ORPHA:221061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0001028	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0001048	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0001324	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0002516	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0002650	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0003401	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0012748	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0012749	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0030430	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0033748	ORPHA:221061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0002572	ORPHA:221061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0007872	ORPHA:221061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0011276	ORPHA:221061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0011513	ORPHA:221061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0012721	ORPHA:221061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221061	Familial cerebral cavernous malformation		HP:0100543	ORPHA:221061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000026	ORPHA:52901	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000134	ORPHA:52901	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0008213	ORPHA:52901	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000044	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000786	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000823	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0002215	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0002225	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0002750	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0008214	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0008734	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0012569	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0040171	ORPHA:52901	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000027	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000029	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000798	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0000876	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0010791	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0012814	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0012864	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency		HP:0030018	ORPHA:52901	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:52901	Isolated follicle stimulating hormone deficiency	NOT	HP:0000458	ORPHA:52901	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0000303	ORPHA:3416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0000407	ORPHA:3416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0000889	ORPHA:3416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0003103	ORPHA:3416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0004437	ORPHA:3416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0005019	ORPHA:3416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0005789	ORPHA:3416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3416	Hyperostosis corticalis generalisata		HP:0010628	ORPHA:3416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0000512	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0000666	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0001139	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0001249	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0001581	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0002046	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0002205	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0003691	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0007476	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0011003	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0030203	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3417	Van den Bosch syndrome		HP:0200016	ORPHA:3417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0000215	ORPHA:79133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0000294	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0000307	ORPHA:79133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0000414	ORPHA:79133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0000437	ORPHA:79133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0000561	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0001057	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0001075	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0001999	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0002714	ORPHA:79133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0005338	ORPHA:79133	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0005585	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0005590	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0008070	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0009743	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0010781	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79133	Focal facial dermal dysplasia type I		HP:0011221	ORPHA:79133	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0003074	ORPHA:79134	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0040217	ORPHA:79134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0001250	ORPHA:79134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0001324	ORPHA:79134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0008936	ORPHA:79134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0011342	ORPHA:79134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0000343	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0000463	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0001488	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0001944	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0002013	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0002521	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0002714	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0003196	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0005487	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0009830	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0009894	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome		HP:0040025	ORPHA:79134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79134	DEND syndrome	NOT	HP:0030057	ORPHA:79134	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0000104	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0001622	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0001623	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0001945	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0003762	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0008670	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0012532	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0012888	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0030016	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0030711	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0100607	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3411	Double uterus-hemivagina-renal agenesis syndrome		HP:0100608	ORPHA:3411	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79135	Episodic ataxia type 3		HP:0002131	ORPHA:79135	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79135	Episodic ataxia type 3		HP:0002321	ORPHA:79135	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79135	Episodic ataxia type 3		HP:0000360	ORPHA:79135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79135	Episodic ataxia type 3		HP:0002411	ORPHA:79135	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79135	Episodic ataxia type 3		HP:0000639	ORPHA:79135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79135	Episodic ataxia type 3		HP:0001250	ORPHA:79135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79135	Episodic ataxia type 3		HP:0002301	ORPHA:79135	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000104	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000238	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000482	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000587	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0001249	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0001511	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0001561	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002023	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002032	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002410	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002575	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0008678	ORPHA:3412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002937	ORPHA:3412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002984	ORPHA:3412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0003312	ORPHA:3412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0030680	ORPHA:3412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000023	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000028	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000278	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000347	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000356	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000528	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0000568	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0001195	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002089	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002139	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002414	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0002827	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0009892	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0010305	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0011027	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0011267	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3412	VACTERL with hydrocephalus		HP:0100541	ORPHA:3412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0001251	ORPHA:79136	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0000617	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0000640	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0000651	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0002172	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0002311	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0002321	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0002359	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0002457	ORPHA:79136	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79136	Episodic ataxia type 4		HP:0002018	ORPHA:79136	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0002197	ORPHA:79137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0007166	ORPHA:79137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0010849	ORPHA:79137	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0000565	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0000639	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0001263	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0001290	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0002069	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0002072	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0002121	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79137	Generalized epilepsy-paroxysmal dyskinesia syndrome		HP:0006889	ORPHA:79137	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0000602	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001251	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001289	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002329	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0003403	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0003431	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0007305	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0032169	ORPHA:79138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0000651	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001284	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002090	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002094	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002270	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002353	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002922	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0003690	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0007131	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0007209	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0007256	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0011947	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0012534	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0012696	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0030057	ORPHA:79138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0000496	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0000508	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0000639	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001259	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001283	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001291	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001315	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0001348	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002273	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002445	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0002878	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0003487	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0004887	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0009916	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0010628	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0010831	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0010871	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0011499	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0012229	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0012416	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0012531	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0030319	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0031123	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79138	Bickerstaff brainstem encephalitis		HP:0100786	ORPHA:79138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0003134	ORPHA:431329	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0003551	ORPHA:431329	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0003698	ORPHA:431329	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0000648	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0001257	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0001258	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0002540	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0003487	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0005109	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0007141	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0007178	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0008944	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0009830	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431329	Autosomal recessive spastic paraplegia type 57		HP:0012447	ORPHA:431329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0000365	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0000518	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0000726	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0001285	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0002073	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0002185	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0002352	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439254	ITM2B amyloidosis		HP:0011970	ORPHA:439254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0001300	ORPHA:454887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0001336	ORPHA:454887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0007158	ORPHA:454887	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0000726	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0000743	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0001288	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0001337	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0002067	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0002172	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0002304	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0002451	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0003474	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0004305	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0007301	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0030217	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0045084	ORPHA:454887	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0001332	ORPHA:454887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0002354	ORPHA:454887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0002381	ORPHA:454887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0011098	ORPHA:454887	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0000708	ORPHA:454887	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:454887	Corticobasal syndrome		HP:0100022	ORPHA:454887	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000028	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000036	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000089	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000113	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000160	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000218	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000233	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000269	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000347	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000369	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000377	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000470	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000772	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000773	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000811	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000879	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000883	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0001195	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0001562	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0001762	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0002009	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0002089	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0002098	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0002107	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0002878	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0002984	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0002990	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0003027	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0003041	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0003309	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0003561	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0000444	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0005280	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0005792	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0006495	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0008665	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0008683	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0008846	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0008897	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0009800	ORPHA:3404	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0009829	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0010049	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0011341	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3404	Ulbright-Hodes syndrome		HP:0040072	ORPHA:3404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0001561	ORPHA:3405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0001903	ORPHA:3405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0002247	ORPHA:3405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0001195	ORPHA:3405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0001629	ORPHA:3405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0001679	ORPHA:3405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0001702	ORPHA:3405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0011100	ORPHA:3405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3405	Umbilical cord ulceration-intestinal atresia syndrome		HP:0001789	ORPHA:3405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0001041	ORPHA:3406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0005338	ORPHA:3406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0007502	ORPHA:3406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0030350	ORPHA:3406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0032152	ORPHA:3406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0045059	ORPHA:3406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0000290	ORPHA:3406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0000306	ORPHA:3406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0000958	ORPHA:3406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0004334	ORPHA:3406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0004426	ORPHA:3406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0001061	ORPHA:3406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0005268	ORPHA:3406	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:3406	Ulerythema ophryogenesis		HP:0032282	ORPHA:3406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0004915	ORPHA:570422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0012024	ORPHA:570422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0012379	ORPHA:570422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0000518	ORPHA:570422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0001396	ORPHA:570422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0001410	ORPHA:570422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0000707	ORPHA:570422	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0001508	ORPHA:570422	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0002240	ORPHA:570422	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:570422	Galactose mutarotase deficiency		HP:0100806	ORPHA:570422	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3408	Upington disease		HP:0002829	ORPHA:3408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3408	Upington disease		HP:0003365	ORPHA:3408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3408	Upington disease		HP:0003370	ORPHA:3408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3408	Upington disease		HP:0006429	ORPHA:3408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3408	Upington disease		HP:0010588	ORPHA:3408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3408	Upington disease		HP:0030038	ORPHA:3408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000028	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000135	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000286	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000288	ORPHA:3409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000347	ORPHA:3409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000426	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000470	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000486	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000939	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000940	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0001156	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0001249	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0001773	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0002757	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0003212	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0004209	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0004322	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0005830	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000069	ORPHA:3409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000396	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0000582	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0001513	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0001770	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0002808	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0005930	ORPHA:3409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0008736	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0009906	ORPHA:3409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3409	Urban-Rogers-Meyer syndrome		HP:0100490	ORPHA:3409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0002315	ORPHA:40923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0007902	ORPHA:40923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0025188	ORPHA:40923	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0000421	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0000501	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0000543	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0000618	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0000707	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0002019	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0002313	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0007052	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0007663	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0007917	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0011497	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0011505	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0011531	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0012122	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0012230	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0030329	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0030652	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0030667	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0030773	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0030786	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0040049	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0100832	ORPHA:40923	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0002140	ORPHA:40923	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0002196	ORPHA:40923	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0002326	ORPHA:40923	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0025239	ORPHA:40923	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:40923	Eales disease		HP:0100014	ORPHA:40923	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0011627	ORPHA:3400	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0001714	ORPHA:3400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0001635	ORPHA:3400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0001654	ORPHA:3400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0001679	ORPHA:3400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0002616	ORPHA:3400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0006704	ORPHA:3400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3400	Aorto-ventricular tunnel		HP:0030148	ORPHA:3400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0003139	ORPHA:79124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0030355	ORPHA:79124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0011117	ORPHA:79124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0040088	ORPHA:79124	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001433	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001531	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002205	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002240	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002743	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002849	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0004429	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0005403	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0012735	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0030374	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0031123	ORPHA:79124	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0000016	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0000952	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001269	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001409	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001541	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001873	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001876	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0001903	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002014	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002069	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002100	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002206	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002385	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002415	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002722	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002728	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0002910	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0010550	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0031218	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0040223	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0100626	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0410018	ORPHA:79124	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0000252	ORPHA:79124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79124	Hepatic veno-occlusive disease-immunodeficiency syndrome		HP:0040089	ORPHA:79124	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002094	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002110	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002113	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002878	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0012418	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0025177	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0025179	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0025392	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0025393	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0030879	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0032177	ORPHA:79126	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0000822	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0000961	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0001945	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002202	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002789	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0012378	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0030830	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0031246	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0045051	ORPHA:79126	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0001698	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002206	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002716	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0002829	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0003259	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0003326	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0003565	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0011227	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0012398	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0031631	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0031851	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0100749	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79126	Acute interstitial pneumonia		HP:0100750	ORPHA:79126	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0031316	ORPHA:3403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0001635	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0001640	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0001698	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0001708	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0005180	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0033138	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0034330	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:6000667	ORPHA:3403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0001279	ORPHA:3403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0001649	ORPHA:3403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0001789	ORPHA:3403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0002202	ORPHA:3403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0010882	ORPHA:3403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly		HP:0011675	ORPHA:3403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:3403	Uhl anomaly	NOT	HP:0034364	ORPHA:3403	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0002091	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0002094	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0002097	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0002207	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0006510	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0025179	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0030828	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0030877	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0031996	ORPHA:79127	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0004469	ORPHA:79127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0006516	ORPHA:79127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0011947	ORPHA:79127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0012418	ORPHA:79127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0031246	ORPHA:79127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0045051	ORPHA:79127	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0001217	ORPHA:79127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0001824	ORPHA:79127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0001945	ORPHA:79127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0002105	ORPHA:79127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0002110	ORPHA:79127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0025175	ORPHA:79127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79127	Respiratory bronchiolitis-interstitial lung disease syndrome		HP:0100749	ORPHA:79127	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0002656	ORPHA:79106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0002829	ORPHA:79106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0006376	ORPHA:79106	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0001169	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0001211	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0001769	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0001773	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0001831	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0002663	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0002753	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0002967	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0003025	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0003038	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0003170	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0003275	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0004279	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0004322	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0008800	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0008808	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0009803	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0010305	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0011849	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79106	Eiken syndrome		HP:0100671	ORPHA:79106	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000158	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000202	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000316	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000348	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000407	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000518	ORPHA:79107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000618	ORPHA:79107	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0000882	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0001249	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0001263	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0001268	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0002015	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0002571	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0002650	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0002721	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0002808	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0002983	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0004322	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0007325	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0008796	ORPHA:79107	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79107	Developmental malformations-deafness-dystonia syndrome		HP:0100613	ORPHA:79107	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0001332	ORPHA:36899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0001336	ORPHA:36899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0010531	ORPHA:36899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0045084	ORPHA:36899	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0000473	ORPHA:36899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0000716	ORPHA:36899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0000722	ORPHA:36899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0000739	ORPHA:36899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0002356	ORPHA:36899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0012075	ORPHA:36899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:36899	Myoclonus-dystonia syndrome		HP:0025269	ORPHA:36899	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000023	ORPHA:325345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000039	ORPHA:325345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000041	ORPHA:325345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000048	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000051	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000054	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000056	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000058	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000062	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000063	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0000150	ORPHA:325345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0001197	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0010459	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0010460	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0010461	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0012244	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0030258	ORPHA:325345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0012861	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:325345	46,XY ovotesticular difference of sex development		HP:0100779	ORPHA:325345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0001161	ORPHA:93405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0001199	ORPHA:93405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0001376	ORPHA:93405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0001501	ORPHA:93405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0001770	ORPHA:93405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0001829	ORPHA:93405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0005736	ORPHA:93405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0010708	ORPHA:93405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93405	Syndactyly type 4		HP:0100490	ORPHA:93405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000286	ORPHA:1698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000358	ORPHA:1698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000369	ORPHA:1698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000431	ORPHA:1698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0001252	ORPHA:1698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0001263	ORPHA:1698	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000316	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000337	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000365	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000470	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000508	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0000639	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0001561	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0001627	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0002650	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0004322	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0007483	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:0100790	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1698	Mosaic trisomy 12 syndrome		HP:6000010	ORPHA:1698	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0001440	ORPHA:93406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0004209	ORPHA:93406	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0004691	ORPHA:93406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0006097	ORPHA:93406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0009465	ORPHA:93406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0009701	ORPHA:93406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0009882	ORPHA:93406	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93406	Syndactyly type 5		HP:0100490	ORPHA:93406	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0004691	ORPHA:93403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0006097	ORPHA:93403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0001773	ORPHA:93403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0001830	ORPHA:93403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0004209	ORPHA:93403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0004279	ORPHA:93403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0005916	ORPHA:93403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0009773	ORPHA:93403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0100490	ORPHA:93403	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0001841	ORPHA:93403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0001852	ORPHA:93403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93403	Syndactyly type 2		HP:0100260	ORPHA:93403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000232	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000252	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000316	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000347	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000348	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000358	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000494	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000581	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0002007	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0002916	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0003196	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0004322	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0005280	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0001382	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0100543	ORPHA:1695	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000028	ORPHA:1695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000218	ORPHA:1695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000248	ORPHA:1695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000444	ORPHA:1695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000767	ORPHA:1695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0002650	ORPHA:1695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0008056	ORPHA:1695	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0000079	ORPHA:1695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1695	Non-distal duplication 10q syndrome		HP:0030680	ORPHA:1695	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93404	Syndactyly type 3		HP:0001831	ORPHA:93404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93404	Syndactyly type 3		HP:0006101	ORPHA:93404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93404	Syndactyly type 3		HP:0100490	ORPHA:93404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93409	Brachydactyly-syndactyly, Zhao type		HP:0001770	ORPHA:93409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93409	Brachydactyly-syndactyly, Zhao type		HP:0001822	ORPHA:93409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93409	Brachydactyly-syndactyly, Zhao type		HP:0004220	ORPHA:93409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93409	Brachydactyly-syndactyly, Zhao type		HP:0004704	ORPHA:93409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93409	Brachydactyly-syndactyly, Zhao type		HP:0009577	ORPHA:93409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93409	Brachydactyly-syndactyly, Zhao type		HP:0009773	ORPHA:93409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93409	Brachydactyly-syndactyly, Zhao type		HP:0010047	ORPHA:93409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0010880	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000776	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001539	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000107	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000568	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0006956	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001274	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001320	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0100490	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001233	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0012553	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0002089	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000280	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0005280	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000431	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000369	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000154	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000308	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001561	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0007759	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000202	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000803	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0007291	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0002280	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000175	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001188	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001838	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000377	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000256	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0002007	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000054	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001166	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001792	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0009943	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001770	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0100040	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0010344	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001837	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0002126	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001321	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0002987	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0003244	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000954	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0010511	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000324	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0007911	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000179	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000188	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001032	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0002943	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0045086	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0004935	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001629	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0002342	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001195	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000237	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0000494	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0001680	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0040019	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1692	Mosaic trisomy 1 syndrome		HP:0100839	ORPHA:1692	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0012735	ORPHA:140896	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0001945	ORPHA:140896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0002094	ORPHA:140896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0002098	ORPHA:140896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0002315	ORPHA:140896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0002721	ORPHA:140896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0003326	ORPHA:140896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0000819	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0001626	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0002664	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0004887	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0006528	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0011949	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0012418	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0025439	ORPHA:140896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:140896	Severe acute respiratory syndrome		HP:0001919	ORPHA:140896	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0100483	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0001839	ORPHA:488232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0008619	ORPHA:488232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0001597	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0004692	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0005767	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0010076	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0010112	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0010359	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0010371	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0010383	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0010413	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488232	Split-foot malformation-mesoaxial polydactyly syndrome		HP:0010711	ORPHA:488232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000175	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000191	ORPHA:79113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000243	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000272	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000286	ORPHA:79113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000327	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000347	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000356	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000369	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000384	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000396	ORPHA:79113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000405	ORPHA:79113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000413	ORPHA:79113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000506	ORPHA:79113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000582	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0000750	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0001177	ORPHA:79113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0001249	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0001250	ORPHA:79113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0001631	ORPHA:79113	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0003196	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0004322	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0005484	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0008551	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0008609	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0009738	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0009748	ORPHA:79113	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0011268	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0011272	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79113	Mandibulofacial dysostosis-microcephaly syndrome		HP:0011968	ORPHA:79113	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93402	Syndactyly type 1		HP:0001770	ORPHA:93402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93402	Syndactyly type 1		HP:0004691	ORPHA:93402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93402	Syndactyly type 1		HP:0006097	ORPHA:93402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93402	Syndactyly type 1		HP:0009773	ORPHA:93402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000232	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000262	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000272	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000286	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000293	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000316	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000347	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000431	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000470	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000474	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000574	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0001176	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0001249	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0001263	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0002714	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0002916	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0003196	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0004209	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0009738	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0012368	ORPHA:1699	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000369	ORPHA:1699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000520	ORPHA:1699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0002750	ORPHA:1699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0004322	ORPHA:1699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0030680	ORPHA:1699	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000079	ORPHA:1699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0000175	ORPHA:1699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0002023	ORPHA:1699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0002558	ORPHA:1699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0008053	ORPHA:1699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1699	Trisomy 12p syndrome		HP:0008056	ORPHA:1699	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000280	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000365	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000369	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000518	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000943	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000969	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001252	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001263	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001433	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001541	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0010729	ORPHA:93400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000023	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000077	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000238	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000486	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000519	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000572	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000639	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000648	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000967	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001009	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001250	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001251	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001257	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001310	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001336	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001537	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0001627	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0002376	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0007750	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0007957	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0009891	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0011947	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0030506	ORPHA:93400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000212	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000256	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0000348	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0002240	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0003115	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0004554	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0010442	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93400	Congenital sialidosis type 2		HP:0010808	ORPHA:93400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000028	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000164	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000219	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000233	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000252	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000486	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000527	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000540	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000574	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000675	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000708	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000729	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000750	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000954	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001249	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001252	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001508	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001518	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001631	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001643	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001852	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001999	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002119	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002719	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0004209	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0010059	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0011968	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0012758	ORPHA:363611	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000023	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000059	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000160	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000175	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000286	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000316	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000322	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000341	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000343	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000348	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000358	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000378	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000455	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000463	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000482	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000490	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000664	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000691	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000938	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000960	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0000998	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001212	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001363	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001653	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001680	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0001741	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002000	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002020	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002092	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002360	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002553	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0002783	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0003196	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0004691	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0006528	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0006579	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0009183	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0011470	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0011800	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0025116	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0025160	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0040223	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363611	CTCF-related neurodevelopmental disorder		HP:0100806	ORPHA:363611	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0010479	ORPHA:431341	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0010881	ORPHA:431341	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0000010	ORPHA:431341	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0002027	ORPHA:431341	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0012618	ORPHA:431341	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0034267	ORPHA:431341	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0100645	ORPHA:431341	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0005420	ORPHA:431341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0010957	ORPHA:431341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:431341	Patent urachus		HP:0032435	ORPHA:431341	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0003207	ORPHA:51608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0004963	ORPHA:51608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0006559	ORPHA:51608	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000121	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000365	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000822	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000961	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001561	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001717	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002098	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002749	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0004912	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0004966	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0010512	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0010766	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0011968	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0012408	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0012457	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0025116	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0025169	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0025477	ORPHA:51608	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000381	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000405	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000407	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000410	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000630	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000737	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000951	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000969	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001384	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001531	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001541	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001640	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001698	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001714	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001789	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001945	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002013	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002815	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002829	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002949	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0003836	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0003941	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0005213	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0009164	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0010639	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0012409	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0032553	ORPHA:51608	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0200067	ORPHA:51608	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0000573	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001102	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001250	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0001297	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002092	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002326	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002514	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0002647	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0003109	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0005103	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0006690	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0011344	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0011506	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0040197	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:51608	Generalized arterial calcification of infancy		HP:0100758	ORPHA:51608	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001647	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001650	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001655	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001663	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001718	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001907	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0004756	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0005182	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0010446	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0011636	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0011662	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0100584	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0003115	ORPHA:1686	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0000775	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001279	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001537	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001539	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001540	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001627	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001629	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001631	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001635	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001651	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001669	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001679	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001680	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001681	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001712	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001962	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0004415	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0004971	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0005301	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0006682	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0006714	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0010773	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0010866	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0011628	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0011675	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0100749	ORPHA:1686	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001634	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001636	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1686	Cardiac diverticulum		HP:0001643	ORPHA:1686	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001999	ORPHA:487796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0410263	ORPHA:487796	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000119	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000766	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000818	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001249	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001627	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001873	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002079	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002119	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002518	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002650	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002719	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0008897	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0011877	ORPHA:487796	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000023	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000047	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000122	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000126	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000154	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000219	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000252	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000316	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000319	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000322	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000341	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000343	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000365	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000358	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000414	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000431	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000454	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000465	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000486	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000494	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000508	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000577	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000582	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000648	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000664	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000687	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000689	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0000924	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001004	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001182	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001250	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001263	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001272	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001305	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001344	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001371	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001643	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0001845	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002465	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002553	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002714	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0002721	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0003764	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0005160	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0007033	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0007655	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0007663	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0008947	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0009623	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0010804	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0011220	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0011800	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0012385	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0030084	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0045075	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487796	Takenouchi-Kosaki syndrome		HP:0100763	ORPHA:487796	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000953	ORPHA:221016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001010	ORPHA:221016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001029	ORPHA:221016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0010783	ORPHA:221016	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000164	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001041	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001510	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001518	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002164	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0004322	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0004334	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0005775	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0008070	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0100840	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0200102	ORPHA:221016	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000028	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000175	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000218	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000282	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000417	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000519	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000670	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000682	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000684	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000691	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0000938	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001373	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001875	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001903	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002013	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002014	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002665	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002669	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002671	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002750	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002756	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002860	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002863	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002970	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0003065	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0003189	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0003995	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0004039	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0004979	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0006443	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0006496	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0007418	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0007556	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0008066	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0008069	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0009803	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0009804	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0010049	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0010978	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0012719	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0031367	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0040288	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0100238	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0100671	ORPHA:221016	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001118	ORPHA:221016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001909	ORPHA:221016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0001915	ORPHA:221016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0002861	ORPHA:221016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0003761	ORPHA:221016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0009700	ORPHA:221016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2		HP:0200044	ORPHA:221016	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221016	Rothmund-Thomson syndrome type 2	NOT	HP:0001249	ORPHA:221016	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1682	Arterial dissection-lentiginosis syndrome		HP:0000995	ORPHA:1682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1682	Arterial dissection-lentiginosis syndrome		HP:0001269	ORPHA:1682	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1682	Arterial dissection-lentiginosis syndrome		HP:0005294	ORPHA:1682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1682	Arterial dissection-lentiginosis syndrome		HP:0100026	ORPHA:1682	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0000175	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0000271	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0000366	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0000478	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0000504	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0001671	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0002323	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0007703	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0000377	ORPHA:1681	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1681	Diprosopus		HP:0100335	ORPHA:1681	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0000154	ORPHA:93474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0000232	ORPHA:93474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0000280	ORPHA:93474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0000407	ORPHA:93474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0000501	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0000924	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0001376	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0001387	ORPHA:93474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0001659	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0001744	ORPHA:93474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0002240	ORPHA:93474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0002313	ORPHA:93474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0007957	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0008155	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0012384	ORPHA:93474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0012471	ORPHA:93474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0040129	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93474	Scheie syndrome		HP:0100021	ORPHA:93474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000158	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000232	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000238	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000268	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000280	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000293	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000365	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000431	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000463	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000470	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000488	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000501	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000574	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000716	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000772	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000822	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000889	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000924	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0000940	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001000	ORPHA:93473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001249	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001252	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001263	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001376	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001510	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001522	ORPHA:93473	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001638	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001654	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001681	ORPHA:93473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001706	ORPHA:93473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0001744	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002007	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002028	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002205	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002230	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002240	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002313	ORPHA:93473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002360	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002650	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0002652	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0003275	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0003416	ORPHA:93473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0003468	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0004322	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0005280	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0005930	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0007256	ORPHA:93473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0007957	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0008155	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0009811	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0011968	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0012384	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0012471	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0040129	ORPHA:93473	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0100021	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0100490	ORPHA:93473	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0100729	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0100765	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93473	Hurler syndrome		HP:0100790	ORPHA:93473	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000252	ORPHA:468631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001999	ORPHA:468631	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000340	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001511	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001525	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002119	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002126	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002465	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002828	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0003510	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0010864	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0011344	ORPHA:468631	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000028	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000047	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000122	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000125	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000160	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000278	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000308	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000315	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000319	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000358	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000426	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000431	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000520	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000543	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000582	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000601	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000609	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000733	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0000964	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001250	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001257	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001260	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001272	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001274	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001276	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001302	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001321	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001339	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0001363	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002059	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002079	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002247	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002360	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002487	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002518	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0002539	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0004742	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0005487	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0006380	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0006466	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0006870	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0006872	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0006955	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0007165	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0007256	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0007333	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0007633	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0007843	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0008619	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0008936	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0009879	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0009905	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0005650	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0010705	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0010767	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0012110	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0012294	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0030260	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0100490	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0100702	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency		HP:0100716	ORPHA:468631	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0000280	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0000407	ORPHA:93476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0001376	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0001638	ORPHA:93476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0001654	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0001744	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0002230	ORPHA:93476	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0002240	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0002652	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0003416	ORPHA:93476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0003468	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0004322	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0007256	ORPHA:93476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0007957	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0012384	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0040129	ORPHA:93476	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0100765	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93476	Hurler-Scheie syndrome		HP:0100790	ORPHA:93476	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0003654	ORPHA:1675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0012127	ORPHA:1675	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001250	ORPHA:1675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001263	ORPHA:1675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001328	ORPHA:1675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002353	ORPHA:1675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0008947	ORPHA:1675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0010841	ORPHA:1675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000194	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000218	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000252	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000256	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000278	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000316	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000463	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000470	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000478	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000482	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000483	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000486	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000494	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000527	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000545	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000639	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000684	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000729	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000737	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001104	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001276	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001284	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001344	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001347	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0001799	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002002	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002033	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002059	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002187	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002373	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002540	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002656	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0002983	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0004887	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0005274	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0005280	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0006191	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0006863	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0000718	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0008872	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0009748	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0011153	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0011220	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0011344	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0012433	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0030890	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1675	Dihydropyrimidine dehydrogenase deficiency		HP:0030939	ORPHA:1675	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000040	ORPHA:1672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000232	ORPHA:1672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000238	ORPHA:1672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000400	ORPHA:1672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000639	ORPHA:1672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000648	ORPHA:1672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000708	ORPHA:1672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000864	ORPHA:1672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0000975	ORPHA:1672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0001176	ORPHA:1672	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0004325	ORPHA:1672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0004326	ORPHA:1672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0004375	ORPHA:1672	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1672	Diencephalic syndrome		HP:0100022	ORPHA:1672	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1671	Split cord malformation type I		HP:0002230	ORPHA:1671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1671	Split cord malformation type I		HP:0002650	ORPHA:1671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1671	Split cord malformation type I		HP:0100563	ORPHA:1671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0100950	ORPHA:71212	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0000825	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001254	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001289	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001319	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001397	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001511	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001985	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001998	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0002013	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0002014	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0002173	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0002910	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0003215	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0003508	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0006929	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0008283	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0012071	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0030781	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0030796	ORPHA:71212	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0000580	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001270	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001508	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001987	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0003128	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0003234	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0008151	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0008180	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0008872	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0009830	ORPHA:71212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001639	ORPHA:71212	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001644	ORPHA:71212	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0001657	ORPHA:71212	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0002605	ORPHA:71212	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0002913	ORPHA:71212	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71212	Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency		HP:0006554	ORPHA:71212	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0007663	ORPHA:71213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0009711	ORPHA:71213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0000501	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0000529	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0000545	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0000618	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0000622	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0000646	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0001147	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0007902	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0008014	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0011532	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0011886	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0012531	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0012803	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0030528	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0030786	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0100014	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71213	Retinal capillary malformation		HP:0100832	ORPHA:71213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000817	ORPHA:468620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0001249	ORPHA:468620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002019	ORPHA:468620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002360	ORPHA:468620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0011344	ORPHA:468620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0410263	ORPHA:468620	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000252	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000712	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000717	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000718	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002066	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002136	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002376	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002719	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0008947	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0010832	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0011968	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0030051	ORPHA:468620	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000256	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000713	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0000729	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0001250	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0001344	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002133	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002141	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002307	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002312	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002317	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0002515	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468620	Intellectual disability-epilepsy-extrapyramidal syndrome		HP:0004305	ORPHA:468620	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279882	Spasmus nutans		HP:0000473	ORPHA:279882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:279882	Spasmus nutans		HP:0000639	ORPHA:279882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:279882	Spasmus nutans		HP:0100022	ORPHA:279882	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0000009	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0000572	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0002529	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0003474	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0010550	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0011096	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0012486	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0030057	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0100653	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0200026	ORPHA:71211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0012443	ORPHA:71211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0033342	ORPHA:71211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0002018	ORPHA:71211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0002878	ORPHA:71211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0012229	ORPHA:71211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0032492	ORPHA:71211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:71211	Neuromyelitis optica spectrum disorder		HP:0100247	ORPHA:71211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0011995	ORPHA:1677	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0030718	ORPHA:1677	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0001279	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0001640	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0001667	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0001678	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0001962	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0002094	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0005110	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0005178	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0005180	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0005345	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0006707	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0011675	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0012664	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0030872	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0031665	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0031667	ORPHA:1677	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0001250	ORPHA:1677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0002202	ORPHA:1677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0002240	ORPHA:1677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0004757	ORPHA:1677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:0012398	ORPHA:1677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1677	Familial idiopathic dilatation of the right atrium		HP:3000042	ORPHA:1677	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0000252	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0000269	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0000834	ORPHA:1665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0001257	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0001357	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0002120	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0001249	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0010515	ORPHA:1665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0010864	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1665	Sporadic fetal brain disruption sequence		HP:0011344	ORPHA:1665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2997	Ptosis-vocal cord paralysis syndrome		HP:0000508	ORPHA:2997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2997	Ptosis-vocal cord paralysis syndrome		HP:0001601	ORPHA:2997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2997	Ptosis-vocal cord paralysis syndrome		HP:0001611	ORPHA:2997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2997	Ptosis-vocal cord paralysis syndrome		HP:0002301	ORPHA:2997	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2997	Ptosis-vocal cord paralysis syndrome		HP:0001622	ORPHA:2997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2997	Ptosis-vocal cord paralysis syndrome		HP:0003510	ORPHA:2997	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0000252	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0000639	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001250	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001263	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001266	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001272	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001319	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001332	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001508	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001733	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001947	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0001992	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0002079	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0002119	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0002161	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0002415	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0002448	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0002470	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0002478	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0003206	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0003234	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0004897	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0010536	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0010967	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0011951	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0012547	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0012751	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:431361	Progressive encephalopathy with leukodystrophy due to DECR deficiency		HP:0100704	ORPHA:431361	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0030053	ORPHA:1662	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000160	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000176	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000316	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000347	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000369	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000494	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000506	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000621	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000883	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000938	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001196	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001511	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001558	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001622	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001643	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0002089	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0002597	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0002804	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0002828	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0004331	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0004334	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0004492	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0005253	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0005267	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0005595	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0006266	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0006645	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0006710	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000962	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0007592	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0008070	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0009924	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0010219	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0010648	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0012478	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0012745	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0025354	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0040189	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0045075	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0200041	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0200102	ORPHA:1662	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000047	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000073	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000453	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000465	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0000695	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001561	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001631	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001651	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001669	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0001799	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0004388	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0004970	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0005659	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0006267	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0008244	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1662	Restrictive dermopathy		HP:0100490	ORPHA:1662	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1661	X-linked corneal dermoid		HP:0000505	ORPHA:1661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1661	X-linked corneal dermoid		HP:0000572	ORPHA:1661	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1661	X-linked corneal dermoid		HP:0000615	ORPHA:1661	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1661	X-linked corneal dermoid		HP:0007957	ORPHA:1661	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000303	ORPHA:1660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000492	ORPHA:1660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000508	ORPHA:1660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000691	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000958	ORPHA:1660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000963	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000966	ORPHA:1660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000968	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0000995	ORPHA:1660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0002209	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0002231	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0002552	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0007477	ORPHA:1660	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0009804	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0100797	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1660	Dermoodontodysplasia		HP:0100798	ORPHA:1660	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000465	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000766	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000767	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001040	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001060	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001376	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0002650	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0006101	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0009756	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0009760	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0009773	ORPHA:2990	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000135	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000202	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000218	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000252	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000276	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000286	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000307	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000316	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000324	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000347	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000365	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000369	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000492	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000494	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000506	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000508	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001511	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001537	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001760	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0002643	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0002804	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0003422	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0004322	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0008065	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0010318	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0011842	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0100022	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0100490	ORPHA:2990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000023	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000028	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000046	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000157	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000175	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000268	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000343	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000364	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000405	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000486	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0000902	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001059	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001288	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001508	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0001646	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0002089	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0002162	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0030680	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0003202	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0003298	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0003764	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0004942	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0008729	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0008736	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0012718	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2990	Autosomal recessive multiple pterygium syndrome		HP:0100543	ORPHA:2990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000243	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000286	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000308	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000358	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000823	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0001249	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0002007	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0004322	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0008046	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0008499	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0008551	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0009775	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0012368	ORPHA:2994	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000164	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000175	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000252	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000316	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000470	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000821	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0001166	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0001376	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0006101	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0030680	ORPHA:2994	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0000494	ORPHA:2994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0001199	ORPHA:2994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0004397	ORPHA:2994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0009882	ORPHA:2994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2994	Short stature-craniofacial anomalies-genital hypoplasia syndrome		HP:0100490	ORPHA:2994	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0000857	ORPHA:1667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001392	ORPHA:1667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001510	ORPHA:1667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002652	ORPHA:1667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0004322	ORPHA:1667	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001875	ORPHA:1667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002654	ORPHA:1667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002910	ORPHA:1667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0003073	ORPHA:1667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0004325	ORPHA:1667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0006554	ORPHA:1667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0100255	ORPHA:1667	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0000083	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0000252	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0000486	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0000821	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0000952	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001249	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001250	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001263	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001324	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001738	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001891	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001944	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001945	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001987	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001993	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002240	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001288	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002719	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002904	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0011787	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0012622	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0100827	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0410263	ORPHA:1667	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001541	ORPHA:1667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001631	ORPHA:1667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0001719	ORPHA:1667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002480	ORPHA:1667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1667	Wolcott-Rallison syndrome		HP:0002902	ORPHA:1667	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000154	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000233	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000278	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000280	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000286	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000293	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000307	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000316	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000343	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000347	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000431	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000437	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000445	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000494	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000506	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000508	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000612	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000637	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001249	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001250	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001263	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001302	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001328	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001339	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001508	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001510	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002000	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002126	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002300	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002381	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002553	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002652	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0005487	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001302	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0010529	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0011968	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0012905	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0040188	ORPHA:2995	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000072	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000126	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000239	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000243	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000252	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000270	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000448	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000470	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001100	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0001387	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002120	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002162	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0003189	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0010935	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0012157	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0030502	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0100308	ORPHA:2995	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000465	ORPHA:2995	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000482	ORPHA:2995	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0000588	ORPHA:2995	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002326	ORPHA:2995	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0002650	ORPHA:2995	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0009942	ORPHA:2995	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2995	Baraitser-Winter cerebrofrontofacial syndrome		HP:0100540	ORPHA:2995	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0001651	ORPHA:1666	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0001627	ORPHA:1666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0003115	ORPHA:1666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0010872	ORPHA:1666	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0001696	ORPHA:1666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0011603	ORPHA:1666	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0000069	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0001743	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0002101	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0002566	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0004414	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0011615	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0011620	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0012210	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0012243	ORPHA:1666	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0000238	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0000384	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0000465	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0000772	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0001263	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0001374	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0001760	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0002245	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0002594	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0003006	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1666	Dextrocardia		HP:0008771	ORPHA:1666	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0001252	ORPHA:363623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0001263	ORPHA:363623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0003236	ORPHA:363623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0003551	ORPHA:363623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0000252	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0000467	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0000518	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0000639	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0001324	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0001638	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0002093	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0003327	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0003388	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0003394	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0003403	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0003546	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0006698	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0007340	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0008959	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0008997	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0009053	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0030192	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0100543	ORPHA:363623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0001249	ORPHA:363623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363623	GMPPB-related limb-girdle muscular dystrophy R19		HP:0001250	ORPHA:363623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0001298	ORPHA:209370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0002093	ORPHA:209370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0002104	ORPHA:209370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0011344	ORPHA:209370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0000252	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0001250	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0001257	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0001510	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0002020	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0002033	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0002069	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0004305	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0008935	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0010843	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0011471	ORPHA:209370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0000218	ORPHA:209370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0002059	ORPHA:209370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0002126	ORPHA:209370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209370	MECP2-related severe neonatal encephalopathy		HP:0010841	ORPHA:209370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1653	Dentin dysplasia		HP:0000682	ORPHA:1653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1653	Dentin dysplasia		HP:0006482	ORPHA:1653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1653	Dentin dysplasia		HP:0011001	ORPHA:1653	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1653	Dentin dysplasia		HP:0100777	ORPHA:1653	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000083	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000092	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000093	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000097	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000114	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000117	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000121	ORPHA:1652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000518	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000787	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0000790	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0001252	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0001256	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002027	ORPHA:1652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002150	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002653	ORPHA:1652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002663	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002748	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002757	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002814	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002749	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002752	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002753	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003355	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003236	ORPHA:1652	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0002979	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003013	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0010580	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003020	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003025	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003029	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003076	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003109	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003126	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0003149	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0031415	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0005576	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0005574	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0012622	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0008732	ORPHA:1652	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1652	Dent disease		HP:0011342	ORPHA:1652	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0000465	ORPHA:2988	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0000248	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0000316	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0000358	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0000508	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0000537	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0000582	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0001249	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0001290	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0002553	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0006247	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0009623	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0009662	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0009836	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0025537	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2988	Pterygium colli-intellectual disability-digital anomalies syndrome		HP:0025538	ORPHA:2988	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2989	Familial pterygium of the conjunctiva		HP:0000478	ORPHA:2989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2989	Familial pterygium of the conjunctiva		HP:0000504	ORPHA:2989	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2989	Familial pterygium of the conjunctiva		HP:0007759	ORPHA:2989	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0000561	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0000822	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0001635	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0001650	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0001653	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0001677	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0001714	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002097	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002155	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002170	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002216	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002223	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002289	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002616	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0002671	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0003124	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0004382	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0004414	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0006739	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0006766	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0008070	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0011040	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0012397	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0030445	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0100324	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0100578	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363618	LMNA-related cardiocutaneous progeria syndrome		HP:0100678	ORPHA:363618	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0000962	ORPHA:79151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0008404	ORPHA:79151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0025092	ORPHA:79151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0025114	ORPHA:79151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0025512	ORPHA:79151	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0001820	ORPHA:79151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0007530	ORPHA:79151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0200035	ORPHA:79151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0200043	ORPHA:79151	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf		HP:0001798	ORPHA:79151	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf	NOT	HP:0001036	ORPHA:79151	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79151	Acrokeratosis verruciformis of Hopf	NOT	HP:0100792	ORPHA:79151	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79152	Disseminated superficial actinic porokeratosis		HP:0200044	ORPHA:79152	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79152	Disseminated superficial actinic porokeratosis		HP:0000992	ORPHA:79152	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79152	Disseminated superficial actinic porokeratosis		HP:0000989	ORPHA:79152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79152	Disseminated superficial actinic porokeratosis		HP:0002860	ORPHA:79152	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0008404	ORPHA:79153	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001598	ORPHA:79153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001803	ORPHA:79153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001807	ORPHA:79153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001808	ORPHA:79153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001816	ORPHA:79153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0100798	ORPHA:79153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0100803	ORPHA:79153	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0002232	ORPHA:79153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0008399	ORPHA:79153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0100797	ORPHA:79153	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001045	ORPHA:79153	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001047	ORPHA:79153	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0001973	ORPHA:79153	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0008064	ORPHA:79153	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia		HP:0011034	ORPHA:79153	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79153	Idiopathic trachyonychia	NOT	HP:0012531	ORPHA:79153	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000252	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000286	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000301	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000347	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000363	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000369	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000405	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000407	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000413	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000494	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000538	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000581	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000601	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000674	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000683	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000684	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000689	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000767	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0000824	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0001245	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0001508	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0001518	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0001773	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0001831	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0001852	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0002705	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0002750	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0002751	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0004322	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0006143	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0006184	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0007481	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0009381	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0010049	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0010487	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0010765	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0011069	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0012428	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0012725	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0012810	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome		HP:0030842	ORPHA:2980	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2980	Acrootoocular syndrome	NOT	HP:0001249	ORPHA:2980	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001298	ORPHA:79155	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0004365	ORPHA:79155	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0000733	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0000958	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001249	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001263	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001276	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001649	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001942	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001947	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0002315	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0002615	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0005957	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0008527	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0010280	ORPHA:79155	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria		HP:0001259	ORPHA:79155	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79155	Hydroxykynureninuria	NOT	HP:0002448	ORPHA:79155	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1659	Dermatoleukodystrophy		HP:0000962	ORPHA:1659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1659	Dermatoleukodystrophy		HP:0001072	ORPHA:1659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1659	Dermatoleukodystrophy		HP:0001249	ORPHA:1659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1659	Dermatoleukodystrophy		HP:0001315	ORPHA:1659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1659	Dermatoleukodystrophy		HP:0001347	ORPHA:1659	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1659	Dermatoleukodystrophy		HP:0012639	ORPHA:1659	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79156	Seizures-intellectual disability due to hydroxylysinuria syndrome		HP:0001249	ORPHA:79156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79156	Seizures-intellectual disability due to hydroxylysinuria syndrome		HP:0002123	ORPHA:79156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79156	Seizures-intellectual disability due to hydroxylysinuria syndrome		HP:0003355	ORPHA:79156	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0000963	ORPHA:1658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0000966	ORPHA:1658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0000988	ORPHA:1658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0001056	ORPHA:1658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0001072	ORPHA:1658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0007477	ORPHA:1658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0008066	ORPHA:1658	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0009775	ORPHA:1658	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1658	Absence of fingerprints-congenital milia syndrome		HP:0100490	ORPHA:1658	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000046	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000135	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000233	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000271	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000322	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000358	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000470	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000490	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0000664	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0001249	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0002162	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0002714	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0002808	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0002857	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0003196	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0003298	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0004349	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0006610	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0008551	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0008625	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0008736	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0010306	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2983	Difference of sex development-intellectual disability syndrome		HP:0010720	ORPHA:2983	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0000164	ORPHA:1657	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0000491	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0000662	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0000677	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0000940	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0000944	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0001155	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0001156	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0001597	ORPHA:1657	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0001760	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0001810	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0001945	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0002650	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0002758	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0002797	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0002829	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0003019	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0008065	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0008368	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0008391	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1657	Dermatoosteolysis, Kirghizian type		HP:0200042	ORPHA:1657	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0000989	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0001025	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0001935	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0002024	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0002757	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0002960	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0008066	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0010783	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0012538	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0012733	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0200037	ORPHA:1656	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0000964	ORPHA:1656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0033565	ORPHA:1656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0033637	ORPHA:1656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:4000026	ORPHA:1656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:4000029	ORPHA:1656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:4000030	ORPHA:1656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:4000031	ORPHA:1656	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0000684	ORPHA:1656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0000820	ORPHA:1656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0000969	ORPHA:1656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0002653	ORPHA:1656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0009722	ORPHA:1656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0100725	ORPHA:1656	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0000707	ORPHA:1656	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1656	Dermatitis herpetiformis		HP:0031446	ORPHA:1656	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0003215	ORPHA:79159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0003234	ORPHA:79159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0045045	ORPHA:79159	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0000750	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0001252	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0001642	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0001644	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0001944	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0002013	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0011342	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79159	Isobutyryl-CoA dehydrogenase deficiency		HP:0012734	ORPHA:79159	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0000561	ORPHA:2985	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0001249	ORPHA:2985	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0002223	ORPHA:2985	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0000252	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0000320	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0000444	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0000501	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0000963	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0001387	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0001508	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0001510	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0001596	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0002478	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0004322	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0004325	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0004423	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0008070	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0009745	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0011832	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2985	Pseudoprogeria syndrome		HP:0045075	ORPHA:2985	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000023	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000028	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000126	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000130	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000148	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000218	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000219	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000316	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000319	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000347	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000369	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000455	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000470	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000494	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000774	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000998	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001090	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001162	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001290	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001399	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001433	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001541	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001561	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001629	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0001744	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0002119	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0002240	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0002901	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0003075	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0003270	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0005469	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0005989	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0006273	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0006521	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0008897	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0009085	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0011027	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0011800	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0012210	ORPHA:1655	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0000054	ORPHA:1655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1655	Müllerian derivatives-lymphangiectasia-polydactyly syndrome		HP:0002243	ORPHA:1655	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001029	ORPHA:221008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001118	ORPHA:221008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000028	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000164	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000519	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000953	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001009	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001010	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001041	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001510	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001518	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002164	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0004322	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0004334	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0005775	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0008070	ORPHA:221008	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000135	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000282	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000670	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000682	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000684	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000691	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000821	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001249	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001263	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001875	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001903	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002013	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002014	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002863	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0007018	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0007418	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0007556	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0008066	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0008069	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0008209	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0009804	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0010978	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0012719	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0020110	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0031367	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0040288	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0100671	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0100840	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0200102	ORPHA:221008	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0000938	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001909	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0001915	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002669	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002671	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002750	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002860	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002861	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0002970	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0003065	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0003761	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0003995	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0004039	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0004979	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0006443	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0009700	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0009803	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0010049	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:221008	Rothmund-Thomson syndrome type 1		HP:0200044	ORPHA:221008	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0000668	ORPHA:397946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001260	ORPHA:397946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001347	ORPHA:397946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002066	ORPHA:397946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002380	ORPHA:397946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002395	ORPHA:397946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002497	ORPHA:397946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002500	ORPHA:397946	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0000252	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0000666	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001257	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001310	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001337	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002072	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002169	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002359	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0003487	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0003693	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0004322	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0011096	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0025357	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0030187	ORPHA:397946	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001256	ORPHA:397946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001263	ORPHA:397946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002080	ORPHA:397946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002317	ORPHA:397946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0007256	ORPHA:397946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0030051	ORPHA:397946	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0000473	ORPHA:397946	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0001272	ORPHA:397946	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0002059	ORPHA:397946	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0007663	ORPHA:397946	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397946	Autosomal spastic paraplegia type 58		HP:0009830	ORPHA:397946	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0010848	ORPHA:64280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0011147	ORPHA:64280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0000980	ORPHA:64280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0007018	ORPHA:64280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0000716	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0000739	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0001249	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0001328	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0002069	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0002373	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0002883	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0007738	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0010522	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0010794	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0011150	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0012433	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0030218	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0031469	ORPHA:64280	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0000020	ORPHA:64280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0006961	ORPHA:64280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:64280	Childhood absence epilepsy		HP:0045084	ORPHA:64280	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001249	ORPHA:397941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001263	ORPHA:397941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001999	ORPHA:397941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0008947	ORPHA:397941	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000316	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000369	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000400	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000494	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001256	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001956	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0002465	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0012301	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0012443	ORPHA:397941	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000219	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000268	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000272	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000307	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000319	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000322	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000331	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000431	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000445	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000448	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000470	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000540	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000708	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000717	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000768	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000973	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001250	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001321	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0001382	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0002007	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0002136	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0002342	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0002591	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0003186	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0004523	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0010801	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0010814	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0010864	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0045075	ORPHA:397941	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000276	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000286	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0000527	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0002322	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0004209	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0004691	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0005469	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0007165	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0007565	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0012471	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:397941	MAN1B1-CDG		HP:0012472	ORPHA:397941	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000077	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000083	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000522	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000545	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000615	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000648	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000708	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000822	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000966	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0000975	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001063	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001100	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001250	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001251	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001252	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001265	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001278	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001288	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001510	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0001649	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002020	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002047	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002103	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002205	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002585	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002650	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002757	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002797	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0002902	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0003457	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0007328	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0007957	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0008872	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0009830	ORPHA:1764	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0010885	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0100820	ORPHA:1764	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1764	Familial dysautonomia		HP:0200020	ORPHA:1764	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0000028	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0000047	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0000508	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0000767	ORPHA:1762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0001288	ORPHA:1762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0001387	ORPHA:1762	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0002167	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0002750	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0002916	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0004299	ORPHA:1762	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0004322	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0010864	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0000232	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0000286	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0000581	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0001263	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0010804	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1762	Proximal Xq28 duplication syndrome		HP:0011344	ORPHA:1762	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0003474	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0003560	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0001761	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0009053	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0100543	ORPHA:459033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0002442	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0010522	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0000736	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0001513	ORPHA:459033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4	NOT	HP:0001009	ORPHA:459033	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0007141	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0002751	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0000570	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0001260	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0001251	ORPHA:459033	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0000657	ORPHA:459033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0009830	ORPHA:459033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0001332	ORPHA:459033	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0002172	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0001780	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459033	Ataxia-oculomotor apraxia type 4		HP:0008955	ORPHA:459033	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000098	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000158	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000179	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000276	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000280	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000293	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000303	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000337	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000400	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000445	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000830	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000845	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000870	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000975	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001072	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001176	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001182	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001386	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001769	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001869	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0002758	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0002829	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0003859	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0004099	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0006191	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0012378	ORPHA:314769	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000044	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000141	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000164	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000664	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000687	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000716	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000739	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000819	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000822	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001231	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001609	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0002007	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0002076	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0002230	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0002808	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0002893	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0003401	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0003416	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0006767	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0008388	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0010535	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0011760	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0012802	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0100021	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0100540	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0100607	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0100829	ORPHA:314769	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000802	ORPHA:314769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0000956	ORPHA:314769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001639	ORPHA:314769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0001653	ORPHA:314769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0007440	ORPHA:314769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0100518	ORPHA:314769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314769	Somatomammotropinoma		HP:0100786	ORPHA:314769	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0000014	ORPHA:247604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0000763	ORPHA:247604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0001257	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0001285	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0001324	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0001347	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0002015	ORPHA:247604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0002064	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0002127	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0002141	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0002193	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0002371	ORPHA:247604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0002464	ORPHA:247604	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0003202	ORPHA:247604	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247604	Juvenile primary lateral sclerosis		HP:0007256	ORPHA:247604	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0000662	ORPHA:79301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0000939	ORPHA:79301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0000952	ORPHA:79301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0000989	ORPHA:79301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0001080	ORPHA:79301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0001394	ORPHA:79301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0001508	ORPHA:79301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0001744	ORPHA:79301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0001892	ORPHA:79301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0001928	ORPHA:79301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0002024	ORPHA:79301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0002239	ORPHA:79301	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0002240	ORPHA:79301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0002910	ORPHA:79301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0006566	ORPHA:79301	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79301	Congenital bile acid synthesis defect type 1		HP:0009830	ORPHA:79301	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0000478	ORPHA:1766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0000486	ORPHA:1766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0000504	ORPHA:1766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0000518	ORPHA:1766	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0001249	ORPHA:1766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0001250	ORPHA:1766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0001251	ORPHA:1766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0001252	ORPHA:1766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0001288	ORPHA:1766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0001347	ORPHA:1766	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0003202	ORPHA:1766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0004322	ORPHA:1766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0100021	ORPHA:1766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1766	Dysequilibrium syndrome		HP:0100022	ORPHA:1766	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0000952	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0001394	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0001396	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0001399	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0001408	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0001433	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0002630	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0002904	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0003155	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0031956	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0031964	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79302	Congenital bile acid synthesis defect type 3		HP:0100508	ORPHA:79302	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0002904	ORPHA:79303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0012379	ORPHA:79303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0200084	ORPHA:79303	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0000952	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0001396	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0001397	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0001399	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0001508	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0001978	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0002240	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0002570	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0002630	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0002908	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0002910	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0003155	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0003256	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0003645	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0006579	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0008151	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0008897	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0025435	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0030984	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0040319	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0100513	ORPHA:79303	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0000107	ORPHA:79303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0002748	ORPHA:79303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79303	Congenital bile acid synthesis defect type 2		HP:0011040	ORPHA:79303	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0001067	ORPHA:252183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0007470	ORPHA:252183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0009732	ORPHA:252183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0012645	ORPHA:252183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0100698	ORPHA:252183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0001291	ORPHA:252183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0003406	ORPHA:252183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0003416	ORPHA:252183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0006751	ORPHA:252183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0006851	ORPHA:252183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0009735	ORPHA:252183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0000256	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0000403	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0002584	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0002751	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0005220	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0007524	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0007576	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0009593	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0011801	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0012289	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0012440	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0100010	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0100013	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0100527	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma		HP:0100551	ORPHA:252183	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma	NOT	HP:0000995	ORPHA:252183	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:252183	Neurofibroma	NOT	HP:0010609	ORPHA:252183	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0003150	ORPHA:35706	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0011021	ORPHA:35706	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0000960	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0001254	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0001263	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0001328	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0001508	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0001993	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0002500	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0002518	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0002919	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0003530	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35706	Glutaric acidemia type 3		HP:0100710	ORPHA:35706	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002104	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002240	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002376	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002483	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002883	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0003348	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0003481	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0003737	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0004885	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0007108	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0012469	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0031434	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0031546	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0100611	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0003200	ORPHA:255210	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0003572	ORPHA:255210	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000816	ORPHA:255210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002490	ORPHA:255210	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000580	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000597	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001250	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001251	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001257	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001276	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001324	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001332	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001508	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002066	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002069	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002072	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002123	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002151	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002572	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0003648	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0007141	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0007183	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0008947	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0011344	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0100660	ORPHA:255210	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000091	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000407	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000510	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000639	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0000648	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001265	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001347	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001399	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001639	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001644	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0001945	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002015	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002045	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255210	Mitochondrial DNA-associated Leigh syndrome		HP:0002094	ORPHA:255210	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0000716	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0000726	ORPHA:178509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0000741	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0000751	ORPHA:178509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0001300	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0001337	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0001824	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0002071	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0002360	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0002615	ORPHA:178509	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:178509	Perry syndrome		HP:0007110	ORPHA:178509	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35701	3-hydroxy-3-methylglutaryl-CoA synthase deficiency		HP:0001250	ORPHA:35701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35701	3-hydroxy-3-methylglutaryl-CoA synthase deficiency		HP:0001939	ORPHA:35701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35701	3-hydroxy-3-methylglutaryl-CoA synthase deficiency		HP:0001943	ORPHA:35701	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0001249	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0001257	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0001263	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0001344	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0001347	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0002079	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0002465	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0003487	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0005484	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0007256	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0012448	ORPHA:397951	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0000238	ORPHA:397951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0000577	ORPHA:397951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0000666	ORPHA:397951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0001647	ORPHA:397951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0001760	ORPHA:397951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0002059	ORPHA:397951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397951	Microcephaly-thin corpus callosum-intellectual disability syndrome		HP:0007703	ORPHA:397951	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000256	ORPHA:357001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0001999	ORPHA:357001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0011220	ORPHA:357001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000276	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000463	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000486	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000494	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000767	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0001249	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0001263	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0007018	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0012719	ORPHA:357001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000158	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000160	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000218	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000219	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000248	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000268	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000272	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000286	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000316	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000319	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000369	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000400	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000490	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000527	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000609	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000639	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000648	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0000957	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0001250	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0001763	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0001852	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0001869	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0002013	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0002014	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0002027	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0003196	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0003396	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0005280	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0007099	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0007333	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0007371	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0010880	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0011968	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0030084	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357001	19p13.13 microdeletion syndrome		HP:0100807	ORPHA:357001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0000639	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0000817	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001251	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001256	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001260	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001263	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001310	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001332	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001347	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0002061	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0002079	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0002080	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0001288	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0002421	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0006808	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0006895	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0007153	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0007281	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0008936	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0030890	ORPHA:438114	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0000252	ORPHA:438114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0002013	ORPHA:438114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0002151	ORPHA:438114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0002506	ORPHA:438114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0007024	ORPHA:438114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0007179	ORPHA:438114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438114	RARS-related autosomal recessive hypomyelinating leukodystrophy		HP:0007359	ORPHA:438114	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001263	ORPHA:35708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0003785	ORPHA:35708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0025455	ORPHA:35708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0000708	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0000737	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0000975	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001249	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001250	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001252	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001270	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001332	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001508	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002020	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002360	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002421	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0010553	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0011968	ORPHA:35708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0000508	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0000616	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0000729	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0000870	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001260	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001315	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001742	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001943	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002015	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002019	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002307	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002353	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002375	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002509	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002615	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0003487	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0004322	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0100660	ORPHA:35708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0001337	ORPHA:35708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0002014	ORPHA:35708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35708	Aromatic L-amino acid decarboxylase deficiency		HP:0034392	ORPHA:35708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001824	ORPHA:440437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002019	ORPHA:440437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002024	ORPHA:440437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002027	ORPHA:440437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0012174	ORPHA:440437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0012378	ORPHA:440437	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0000708	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0000716	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0000737	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0000739	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001250	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001252	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001276	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002017	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002076	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002239	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002516	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0007018	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0100743	ORPHA:440437	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0000505	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0000738	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001123	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001260	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001288	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001371	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0001402	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002167	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002354	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002376	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002671	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002893	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0002894	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0003006	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0003401	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0004374	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0006725	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0007256	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0010524	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0010526	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0010622	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0010786	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0012113	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0100031	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0100273	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0100571	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0100576	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0100660	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0100835	ORPHA:440437	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0010784	ORPHA:440437	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X		HP:0012126	ORPHA:440437	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X	NOT	HP:0009726	ORPHA:440437	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X	NOT	HP:0100013	ORPHA:440437	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:440437	Familial colorectal cancer Type X	NOT	HP:0100615	ORPHA:440437	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000232	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000316	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000347	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000348	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000431	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000470	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000582	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0001263	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0001328	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0002916	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0010751	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0100818	ORPHA:1752	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000028	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000175	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000190	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000218	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000358	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000411	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0001387	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0008736	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0010297	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0030680	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0100335	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0100627	ORPHA:1752	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0000202	ORPHA:1752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0001156	ORPHA:1752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0002475	ORPHA:1752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0006191	ORPHA:1752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0012062	ORPHA:1752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1752	Trisomy 8q syndrome		HP:0100490	ORPHA:1752	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0001508	ORPHA:35710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0001824	ORPHA:35710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0001944	ORPHA:35710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0002014	ORPHA:35710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0033310	ORPHA:35710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0003228	ORPHA:35710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0003270	ORPHA:35710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0004395	ORPHA:35710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0000083	ORPHA:35710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0000787	ORPHA:35710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0002013	ORPHA:35710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0003072	ORPHA:35710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0030143	ORPHA:35710	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0000790	ORPHA:35710	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:35710	Glucose-galactose malabsorption		HP:0001945	ORPHA:35710	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0000921	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0001651	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0001702	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0002093	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0002240	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0002435	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0002566	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0007477	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0100490	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0100555	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0100563	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1759	Thoraco-abdominal enteric duplication		HP:0100867	ORPHA:1759	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1757	Fibular dimelia-diplopodia syndrome		HP:0009556	ORPHA:1757	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1757	Fibular dimelia-diplopodia syndrome		HP:0000271	ORPHA:1757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1757	Fibular dimelia-diplopodia syndrome		HP:0030736	ORPHA:1757	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0000028	ORPHA:1756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0000036	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0000073	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0000078	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0001539	ORPHA:1756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0002414	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0002475	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0003422	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0003762	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0005107	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0008678	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0009791	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0100561	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0100589	ORPHA:1756	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1756	Caudal duplication		HP:0100668	ORPHA:1756	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35737	Morning glory disc anomaly		HP:0000486	ORPHA:35737	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35737	Morning glory disc anomaly		HP:0000518	ORPHA:35737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35737	Morning glory disc anomaly		HP:0000541	ORPHA:35737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35737	Morning glory disc anomaly		HP:0000588	ORPHA:35737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35737	Morning glory disc anomaly		HP:0000639	ORPHA:35737	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35737	Morning glory disc anomaly		HP:0000646	ORPHA:35737	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35737	Morning glory disc anomaly		HP:0007703	ORPHA:35737	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000093	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000280	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000943	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001263	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001371	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001433	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001873	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001903	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002086	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002205	ORPHA:505248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000100	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000158	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000648	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001072	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001265	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001344	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001387	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001627	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001631	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001635	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001639	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001643	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001649	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001882	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002092	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002098	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002159	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002540	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0003073	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0003541	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0006536	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0031123	ORPHA:505248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000105	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000238	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000286	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000293	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000470	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000506	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000509	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000527	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000629	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000639	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000768	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0000998	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001252	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001552	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001653	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001655	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0001928	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002514	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002652	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002938	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0002942	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0003196	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0003496	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0004315	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0005180	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0005528	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0006191	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0007703	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0008454	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0010307	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0011220	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0012444	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0012448	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0012471	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0012597	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0100790	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0100806	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0100874	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505248	Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders		HP:0410263	ORPHA:505248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:155878	Submucosal cleft palate		HP:0000193	ORPHA:155878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:155878	Submucosal cleft palate		HP:0001611	ORPHA:155878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:155878	Submucosal cleft palate		HP:0011469	ORPHA:155878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:155878	Submucosal cleft palate		HP:5201016	ORPHA:155878	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:155878	Submucosal cleft palate		HP:0000365	ORPHA:155878	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:155878	Submucosal cleft palate		HP:0000403	ORPHA:155878	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231237	Delta-beta-thalassemia		HP:0001903	ORPHA:231237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231237	Delta-beta-thalassemia		HP:0001935	ORPHA:231237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231237	Delta-beta-thalassemia		HP:0011902	ORPHA:231237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0000549	ORPHA:363710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0002396	ORPHA:363710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0002527	ORPHA:363710	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0000407	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0000666	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0001288	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0001336	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0001337	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0002075	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0002078	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0002167	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0002168	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0002406	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0003474	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0006855	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363710	Spinocerebellar ataxia type 37		HP:0100275	ORPHA:363710	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0000256	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0000268	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0000311	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0000316	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0000411	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0000508	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0001513	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0002007	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0002119	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0002376	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0002650	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0002916	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0004322	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0005916	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0008678	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0008736	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1742	Trisomy 5p syndrome		HP:0010864	ORPHA:1742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0001263	ORPHA:485350	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000708	ORPHA:485350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0001250	ORPHA:485350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002120	ORPHA:485350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002342	ORPHA:485350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002500	ORPHA:485350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0010864	ORPHA:485350	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000252	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000256	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000486	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000716	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000718	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000722	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000729	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000739	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000752	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0001336	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002020	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002061	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002069	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002073	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002079	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002119	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002121	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002384	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002650	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0006970	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0007302	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0008947	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0011167	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0011193	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0011968	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0012448	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0012469	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0100704	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0100716	ORPHA:485350	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000023	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000028	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000276	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0000307	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0001763	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002072	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0002317	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0006986	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485350	CLCN4-related X-linked intellectual disability syndrome		HP:0011800	ORPHA:485350	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0001511	ORPHA:1747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0007483	ORPHA:1747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0007988	ORPHA:1747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0008897	ORPHA:1747	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000023	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000110	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000175	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000256	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000324	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000347	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000822	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0000998	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0001518	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0001622	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0001627	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0006297	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0010878	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1747	Mosaic trisomy 7 syndrome		HP:0011342	ORPHA:1747	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000160	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000233	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000307	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000347	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000426	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000470	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000499	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000508	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000581	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000958	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000960	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0001263	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0001511	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0002213	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0002916	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0004322	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0011362	ORPHA:1745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000369	ORPHA:1745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000486	ORPHA:1745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000639	ORPHA:1745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0002007	ORPHA:1745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0009896	ORPHA:1745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0009906	ORPHA:1745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0100818	ORPHA:1745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000079	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000089	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000126	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0000518	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0002101	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0006610	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0008056	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0030680	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1745	Distal duplication 6p syndrome		HP:0100790	ORPHA:1745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231242	Hemoglobin C-beta-thalassemia syndrome		HP:0001744	ORPHA:231242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231242	Hemoglobin C-beta-thalassemia syndrome		HP:0001903	ORPHA:231242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231242	Hemoglobin C-beta-thalassemia syndrome		HP:0001935	ORPHA:231242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231242	Hemoglobin C-beta-thalassemia syndrome		HP:0011902	ORPHA:231242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0001284	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0002380	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0002505	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0003391	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0003394	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0003445	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0003551	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0007126	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0012378	ORPHA:209335	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0001337	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0001387	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0001883	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0002362	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0002486	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0002515	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0003236	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0003484	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0007340	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy		HP:0008981	ORPHA:209335	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:209335	Autosomal dominant adult-onset proximal spinal muscular atrophy	NOT	HP:0002483	ORPHA:209335	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0000197	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0000364	ORPHA:252164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0000769	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0000834	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0001291	ORPHA:252164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0001392	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0001600	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0002011	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0002031	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0002321	ORPHA:252164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0002991	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0003489	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0009588	ORPHA:252164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0009593	ORPHA:252164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0009911	ORPHA:252164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0010628	ORPHA:252164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0010826	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0012531	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0030177	ORPHA:252164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0012533	ORPHA:252164	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0100008	ORPHA:252164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0100011	ORPHA:252164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0100582	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma	NOT	HP:0100697	ORPHA:252164	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:252164	Benign schwannoma		HP:0200008	ORPHA:252164	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0000253	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0000708	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0012760	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0001250	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0001252	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0001263	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0002376	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0010864	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0012171	ORPHA:397933	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0000347	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0000400	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0000486	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0000666	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0001344	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0002487	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0030215	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397933	Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome		HP:0100716	ORPHA:397933	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231249	Hemoglobin E-beta-thalassemia syndrome		HP:0001903	ORPHA:231249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231249	Hemoglobin E-beta-thalassemia syndrome		HP:0002721	ORPHA:231249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231249	Hemoglobin E-beta-thalassemia syndrome		HP:0003281	ORPHA:231249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231249	Hemoglobin E-beta-thalassemia syndrome		HP:0011902	ORPHA:231249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000316	ORPHA:363700	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000957	ORPHA:363700	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000256	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000280	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000475	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000924	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000997	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001176	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001252	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001328	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001382	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001627	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001833	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001999	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0002650	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0007018	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0009088	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0009737	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0011407	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0012062	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0012758	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0030052	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0100698	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0410263	ORPHA:363700	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000218	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000276	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000286	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000324	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000341	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000343	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000347	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000411	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000601	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000767	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001249	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001250	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001263	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001761	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0002057	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0002079	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0002857	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0004322	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0006479	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0009734	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0009735	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0010794	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0012210	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0012471	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0100697	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0430022	ORPHA:363700	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000126	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000238	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0000246	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001028	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001629	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001631	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001634	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001639	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001642	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001653	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0001655	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0002315	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0002751	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0002992	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0003307	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0008678	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0012733	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0020035	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0030426	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0032252	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363700	Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion		HP:0100008	ORPHA:363700	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000280	ORPHA:363705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000998	ORPHA:363705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0004540	ORPHA:363705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0100874	ORPHA:363705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000343	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000969	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000973	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001015	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001250	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001252	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001263	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001382	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001561	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001622	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001640	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001643	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001698	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002020	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002076	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002094	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002098	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002315	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0003546	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0005280	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0007517	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0030890	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0100678	ORPHA:363705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000158	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000286	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000294	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000316	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000520	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000768	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001269	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001297	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001328	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001520	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001635	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001650	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001653	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001654	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002092	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002239	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002579	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002650	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002652	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002708	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0004322	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0004532	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0004944	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0005314	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0006094	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0011220	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0011675	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0011726	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0012471	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0012568	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0100659	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0100790	ORPHA:363705	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000212	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000938	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0000939	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001176	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001256	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001629	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001631	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001647	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0001680	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363705	Craniofaciofrontodigital syndrome		HP:0002021	ORPHA:363705	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0000708	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0001328	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0002069	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0002421	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0008947	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0010844	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0010864	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0012736	ORPHA:289266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0001265	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0001276	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0001336	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0001518	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0001761	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0001999	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0002079	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0002342	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0002373	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0002506	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0003196	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0004322	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0005484	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0007359	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0008936	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0010818	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0011097	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0011451	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0012171	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0012447	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:289266	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation		HP:0012547	ORPHA:289266	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85197	Genochondromatosis type 1		HP:0000889	ORPHA:85197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85197	Genochondromatosis type 1		HP:0002815	ORPHA:85197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85197	Genochondromatosis type 1		HP:0005701	ORPHA:85197	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0000926	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0001249	ORPHA:85198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0001373	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002514	ORPHA:85198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002650	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002657	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002750	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002751	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002758	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002761	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002857	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002879	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0002991	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0003037	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0003422	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0004039	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0004322	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0005701	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0005868	ORPHA:85198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0012221	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0100559	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0100777	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85198	Dysspondyloenchondromatosis		HP:0200041	ORPHA:85198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000047	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000174	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000248	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000260	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000270	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000561	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000682	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000889	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000964	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0002007	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0002023	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0002223	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0002697	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0002750	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0004397	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0004440	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0004491	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0006482	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0006660	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0008368	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0010306	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0012742	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0100589	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0200044	ORPHA:85199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000154	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000272	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000347	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000365	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000520	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0001249	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0001263	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0012471	ORPHA:85199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0000175	ORPHA:85199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0001357	ORPHA:85199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85199	Craniosynostosis-anal anomalies-porokeratosis syndrome		HP:0002808	ORPHA:85199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85193	Idiopathic juvenile osteoporosis		HP:0000939	ORPHA:85193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85193	Idiopathic juvenile osteoporosis		HP:0001288	ORPHA:85193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85193	Idiopathic juvenile osteoporosis		HP:0002653	ORPHA:85193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85193	Idiopathic juvenile osteoporosis		HP:0002757	ORPHA:85193	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85193	Idiopathic juvenile osteoporosis		HP:0002808	ORPHA:85193	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85193	Idiopathic juvenile osteoporosis		HP:0002953	ORPHA:85193	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000233	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000297	ORPHA:85194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000316	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000343	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000369	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000391	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000465	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000470	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000518	ORPHA:85194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000534	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000541	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000545	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000568	ORPHA:85194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000572	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000639	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000926	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000939	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0000974	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0001249	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0001629	ORPHA:85194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0001763	ORPHA:85194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0002162	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0002942	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0003521	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0004322	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0004467	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0005108	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0001382	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0007730	ORPHA:85194	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0008063	ORPHA:85194	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85194	Spondylo-ocular syndrome		HP:0009738	ORPHA:85194	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000164	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000174	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000252	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000294	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000311	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000316	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000319	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000358	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000400	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000470	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000574	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000670	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0001252	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0002916	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0004322	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0005280	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0006610	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0009738	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0010720	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0100543	ORPHA:1738	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000028	ORPHA:1738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000486	ORPHA:1738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0002650	ORPHA:1738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0002750	ORPHA:1738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0100490	ORPHA:1738	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000047	ORPHA:1738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0000581	ORPHA:1738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0001177	ORPHA:1738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0006433	ORPHA:1738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1738	Trisomy 4p syndrome		HP:0030680	ORPHA:1738	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000657	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001249	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001251	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001252	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001263	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001320	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002104	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002793	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002876	ORPHA:475	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000276	ORPHA:475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000639	ORPHA:475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001288	ORPHA:475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0004422	ORPHA:475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0008872	ORPHA:475	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000202	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000238	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000369	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000426	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000463	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000486	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000508	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000612	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0000864	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001161	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001250	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001337	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001696	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0001829	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002084	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002126	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002251	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002269	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002553	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0002650	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0003312	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0007370	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:475	Isolated Joubert syndrome		HP:0030680	ORPHA:475	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000083	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000090	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000112	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000766	ORPHA:474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000772	ORPHA:474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000774	ORPHA:474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000889	ORPHA:474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0000944	ORPHA:474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0001156	ORPHA:474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0001162	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0001392	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0001770	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0001773	ORPHA:474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0001830	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0002093	ORPHA:474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0002644	ORPHA:474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0002652	ORPHA:474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0002983	ORPHA:474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0004322	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0006703	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0007703	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0008872	ORPHA:474	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0010306	ORPHA:474	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:474	Jeune syndrome		HP:0010579	ORPHA:474	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0011496	ORPHA:477	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000164	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000399	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000491	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000509	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000572	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000613	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000653	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000982	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001097	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001581	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0004552	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0005328	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0007431	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0007502	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008070	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008404	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008625	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0011859	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0025092	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0032107	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0040189	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0045075	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0200020	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0200035	ORPHA:477	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000966	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001369	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001508	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001805	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0003765	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0005401	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0005406	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008038	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008897	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0011370	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0012758	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0025084	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0025610	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0030318	ORPHA:477	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0000230	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001305	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001320	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0001999	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0002673	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0002860	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0003065	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0006380	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008069	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008138	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0008788	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0009830	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0011220	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0012844	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0030839	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0031250	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0040154	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0100648	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0100806	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0100838	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:477	KID syndrome		HP:0200036	ORPHA:477	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001508	ORPHA:470	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000091	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000093	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000099	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000121	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000124	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000790	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000938	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000939	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001249	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001394	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001399	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001433	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001510	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001873	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001882	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001892	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001903	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001987	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002013	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002014	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002093	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002154	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002155	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002240	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002570	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002750	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002910	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003124	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003141	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003217	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003233	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003268	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003297	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003348	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0006517	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0006530	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0008358	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0008947	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0011966	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0011968	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0012156	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0012213	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0012278	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0012523	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0012622	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0025435	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0031020	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0100543	ORPHA:470	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000822	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001254	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001259	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001627	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001733	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001917	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001947	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0001970	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002206	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003218	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003281	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003532	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0005368	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0005548	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0010701	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0011424	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0011900	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0012280	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0012578	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0020151	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0030760	ORPHA:470	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0000824	ORPHA:470	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002718	ORPHA:470	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0002756	ORPHA:470	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0003493	ORPHA:470	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0004313	ORPHA:470	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0004431	ORPHA:470	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:470	Lysinuric protein intolerance		HP:0010702	ORPHA:470	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0000093	ORPHA:567548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0003073	ORPHA:567548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0003119	ORPHA:567548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0031265	ORPHA:567548	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0000097	ORPHA:567548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0000969	ORPHA:567548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0002155	ORPHA:567548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0003124	ORPHA:567548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0012579	ORPHA:567548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0100724	ORPHA:567548	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0001919	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0001945	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0002027	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0002315	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0003774	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0011947	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0012590	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0031504	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0100539	ORPHA:567548	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0001510	ORPHA:567548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0001967	ORPHA:567548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0002204	ORPHA:567548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0002586	ORPHA:567548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567548	Idiopathic steroid-resistant nephrotic syndrome		HP:0004936	ORPHA:567548	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0000938	ORPHA:29073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002756	ORPHA:29073	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0000100	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0000112	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0000980	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0001903	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0001919	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002152	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002653	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002797	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0003237	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0003259	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0003324	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0004313	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0012378	ORPHA:29073	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0000014	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0000098	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0001824	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002176	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002808	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002953	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0003072	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0003261	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0003401	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0004341	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0009830	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0012185	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0012719	ORPHA:29073	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0001744	ORPHA:29073	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002202	ORPHA:29073	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:29073	Multiple myeloma		HP:0002716	ORPHA:29073	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000980	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0004823	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0004840	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0010972	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0011904	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0011905	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0025066	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0025547	ORPHA:231214	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000164	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000939	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000953	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001510	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001531	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001744	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001971	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001978	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0002094	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0002240	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0002857	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0006487	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0009004	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0011031	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0011842	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0011968	ORPHA:231214	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000582	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000737	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000819	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000821	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000823	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000829	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000952	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001394	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001395	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001433	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001644	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001722	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001954	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0002007	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0002014	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0002829	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0004936	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0005280	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0010620	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0031035	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0040075	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0200042	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0430028	ORPHA:231214	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0000846	ORPHA:231214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0001402	ORPHA:231214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231214	Beta-thalassemia major		HP:0011675	ORPHA:231214	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0000969	ORPHA:567546	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0012592	ORPHA:567546	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0000097	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0000282	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0003073	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0003077	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0010741	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0012378	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0012622	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0100540	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0100724	ORPHA:567546	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0000034	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0000822	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0002027	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0002094	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0002907	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0003774	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0011947	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0012393	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0012579	ORPHA:567546	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0001541	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0002202	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0002204	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0004420	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0004431	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0004936	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0012050	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567546	Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance		HP:0012587	ORPHA:567546	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0000571	ORPHA:527497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0000639	ORPHA:527497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001251	ORPHA:527497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0007256	ORPHA:527497	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001260	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001263	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001290	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001332	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001347	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0002191	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001288	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0002415	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0002599	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0003429	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0007704	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0030890	ORPHA:527497	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0000486	ORPHA:527497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001007	ORPHA:527497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001250	ORPHA:527497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001272	ORPHA:527497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0002059	ORPHA:527497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0002650	ORPHA:527497	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0001249	ORPHA:527497	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy		HP:0002079	ORPHA:527497	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:527497	NKX6-2-related autosomal recessive hypomyelinating leukodystrophy	NOT	HP:0012534	ORPHA:527497	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000093	ORPHA:567544	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000083	ORPHA:567544	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000100	ORPHA:567544	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000822	ORPHA:567544	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0004431	ORPHA:567544	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0005421	ORPHA:567544	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0045042	ORPHA:567544	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000099	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000155	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000988	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0001369	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0001919	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0001966	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0002907	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0003259	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0012576	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0045073	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0100769	ORPHA:567544	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0000707	ORPHA:567544	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy		HP:0002715	ORPHA:567544	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy	NOT	HP:0002960	ORPHA:567544	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:567544	Idiopathic non-lupus full-house nephropathy	NOT	HP:0020151	ORPHA:567544	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0002668	ORPHA:29072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0006737	ORPHA:29072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0006748	ORPHA:29072	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0000093	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0000096	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0000740	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001069	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001095	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001342	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001618	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001824	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001962	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0002018	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0002331	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0002574	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0002640	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0002864	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0003072	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0003345	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0003574	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0003639	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0008629	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0010532	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0011703	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0011979	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0012378	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0031284	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0100749	ORPHA:29072	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0000405	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0000790	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0000980	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001293	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001337	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001605	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0001635	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0003528	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0005584	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0009711	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0012222	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0025269	ORPHA:29072	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29072	Hereditary pheochromocytoma-paraganglioma		HP:0000526	ORPHA:29072	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0000256	ORPHA:459074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0000337	ORPHA:459074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0001274	ORPHA:459074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0000316	ORPHA:459074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0001256	ORPHA:459074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0001357	ORPHA:459074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0007099	ORPHA:459074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0000324	ORPHA:459074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0002197	ORPHA:459074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459074	Corpus callosum agenesis-macrocephaly-hypertelorism syndrome		HP:0006889	ORPHA:459074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000126	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000175	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000252	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000275	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000286	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000316	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000319	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000347	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000348	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000365	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000445	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000457	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000494	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000508	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000600	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000717	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000722	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000733	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000739	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0000750	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001249	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001250	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001252	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001263	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001510	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001611	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001629	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001636	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0001669	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0002167	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0002650	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0004383	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0007018	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0008661	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0009908	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0010515	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0010978	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0011611	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0011800	ORPHA:1727	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1727	22q11.2 duplication syndrome		HP:0100627	ORPHA:1727	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001250	ORPHA:459070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001999	ORPHA:459070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0010864	ORPHA:459070	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000028	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000252	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000303	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000400	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000717	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000750	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001251	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001321	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001344	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001510	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0002020	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0002650	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0002655	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0008947	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0040080	ORPHA:459070	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000023	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000047	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000160	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000219	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000232	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000268	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000276	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000286	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000308	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000319	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000337	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000343	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000369	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000407	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000411	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000510	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000545	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000577	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000823	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000939	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000954	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0000960	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001007	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001182	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001561	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001601	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001629	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001631	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0001770	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0002069	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0002373	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0002540	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0002719	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0004209	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0004415	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0005750	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0006698	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0007359	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0008734	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0009381	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0010818	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0012032	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0012811	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0031535	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome		HP:0045025	ORPHA:459070	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0030084	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0030732	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0410030	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome	NOT	HP:0001249	ORPHA:1724	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0008947	ORPHA:1724	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000278	ORPHA:1724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0002143	ORPHA:1724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0007483	ORPHA:1724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0007535	ORPHA:1724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0011342	ORPHA:1724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0012450	ORPHA:1724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0200021	ORPHA:1724	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000028	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000077	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000085	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000175	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000347	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000365	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000472	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000486	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000582	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000750	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0000774	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0001252	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0001260	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0001270	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0001328	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0001511	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0001629	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0001633	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0002650	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0002808	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0002948	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0002949	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0003416	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0003422	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0004484	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0006394	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1724	Mosaic trisomy 20 syndrome		HP:0006610	ORPHA:1724	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0003316	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0003320	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0003416	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0003417	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0003467	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0004695	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0004887	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0008417	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0008434	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0008445	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0008469	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0008754	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0009107	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0009928	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0010171	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0010255	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0010646	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0025426	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:3000052	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000518	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000609	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0001629	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0001631	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0001643	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002020	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0004415	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0007766	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0011968	ORPHA:79345	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata	NOT	HP:0010880	ORPHA:79345	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002871	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002947	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000327	ORPHA:79345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0003196	ORPHA:79345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0009882	ORPHA:79345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0012379	ORPHA:79345	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000410	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000455	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000457	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000925	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0001857	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002000	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0003508	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0008420	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0008897	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0010655	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0010666	ORPHA:79345	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0000919	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0001263	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0001742	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002099	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002205	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002341	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002643	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002777	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002787	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79345	Brachytelephalangic chondrodysplasia punctata		HP:0002789	ORPHA:79345	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0000252	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0000316	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0001511	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0001562	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0002194	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0008897	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0011800	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0100790	ORPHA:1723	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0000175	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0000268	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0000568	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0001177	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0001627	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0002119	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0002251	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0002414	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0002566	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0002650	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0002984	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0003022	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0012758	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0033725	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0045005	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1723	Mosaic trisomy 2 syndrome		HP:0410030	ORPHA:1723	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002027	ORPHA:469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0012545	ORPHA:469	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0001510	ORPHA:469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002014	ORPHA:469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002018	ORPHA:469	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0000083	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0000952	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0001069	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0001942	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002013	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002019	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002148	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002149	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002240	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0002918	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0003256	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0003270	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0012051	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0012622	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0100626	ORPHA:469	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0000518	ORPHA:469	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0001250	ORPHA:469	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0001254	ORPHA:469	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:469	Hereditary fructose intolerance		HP:0001259	ORPHA:469	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000202	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000364	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000486	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000491	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000505	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000518	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000532	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000541	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000554	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000568	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000573	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000592	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000668	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000682	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000684	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000962	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000975	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0000988	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001000	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001053	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001231	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001249	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001250	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001252	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001257	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001263	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001288	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001537	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001595	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001596	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001597	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001635	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001804	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001810	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001821	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0001880	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0002092	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0002120	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0002383	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0002558	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0002637	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0002650	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0002797	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0003298	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0004050	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0004097	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0004322	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0004374	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0005815	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0005922	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0006101	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0006482	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0007018	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0007400	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0007850	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0007957	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0008066	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0008388	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0008402	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0010783	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0010978	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0100490	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0100543	ORPHA:464	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0100555	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0100585	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0200042	ORPHA:464	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464	Incontinentia pigmenti		HP:0200043	ORPHA:464	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0003642	ORPHA:79326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0012379	ORPHA:79326	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000252	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000286	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000431	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000494	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000518	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000565	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000612	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0000707	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0001249	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0001250	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0001263	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0001928	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0001999	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0002521	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0011344	ORPHA:79326	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0002079	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0002240	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0006808	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0006956	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0012469	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0012704	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0012751	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79326	ALG2-CDG		HP:0030890	ORPHA:79326	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001249	ORPHA:79327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001250	ORPHA:79327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001252	ORPHA:79327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001263	ORPHA:79327	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000253	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000478	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000486	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000924	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001256	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001871	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001999	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002028	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002650	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0003073	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0011024	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0011344	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0410263	ORPHA:79327	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000077	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000083	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000100	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0000639	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001272	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001376	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001410	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001627	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0001638	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002059	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002243	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002719	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002721	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002808	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0002878	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79327	ALG1-CDG		HP:0100806	ORPHA:79327	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000726	ORPHA:466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0001336	ORPHA:466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0012332	ORPHA:466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0100785	ORPHA:466	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000712	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000716	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000738	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000739	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000822	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000975	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0001251	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0001260	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0001649	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0002015	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0002071	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0006511	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0006979	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0009926	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0010535	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0012660	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0031843	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0033687	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0100543	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:5200044	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:5200360	ORPHA:466	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0000651	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0001824	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0001945	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0002019	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0002371	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0003118	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0007256	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia		HP:0012689	ORPHA:466	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:466	Fatal familial insomnia	NOT	HP:0010850	ORPHA:466	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001249	ORPHA:79328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001250	ORPHA:79328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001263	ORPHA:79328	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000253	ORPHA:79328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001252	ORPHA:79328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001627	ORPHA:79328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001698	ORPHA:79328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002240	ORPHA:79328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002652	ORPHA:79328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0003186	ORPHA:79328	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000105	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000126	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000154	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000193	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000219	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000248	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000260	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000270	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000308	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000316	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000319	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000343	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000347	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000358	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000369	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000430	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000444	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000470	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000473	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000474	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000506	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000520	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000565	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000586	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000737	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000813	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0000998	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001234	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001272	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001347	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001405	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001407	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001539	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001558	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001562	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001629	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001631	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001762	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0001789	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002007	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002013	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002014	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002020	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002059	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002061	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002089	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002099	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002101	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002162	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002265	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0002557	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0003015	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0003026	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0003196	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0003375	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0005133	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0005180	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0005280	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0005343	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0005487	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0007385	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0008724	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0008776	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0008905	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0009004	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0009125	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0009487	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0010763	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0011103	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0011473	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0011849	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0012448	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0012704	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0030215	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0032464	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79328	ALG9-CDG		HP:0100865	ORPHA:79328	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0011854	ORPHA:465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0012233	ORPHA:465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0100310	ORPHA:465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency	NOT	HP:0007420	ORPHA:465	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0001934	ORPHA:465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0004846	ORPHA:465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0040228	ORPHA:465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0040230	ORPHA:465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0040245	ORPHA:465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0040248	ORPHA:465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0040249	ORPHA:465	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0000132	ORPHA:465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0001622	ORPHA:465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0001933	ORPHA:465	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0005268	ORPHA:465	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0000421	ORPHA:465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0002170	ORPHA:465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0002239	ORPHA:465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0006298	ORPHA:465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0011891	ORPHA:465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0030657	ORPHA:465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0040184	ORPHA:465	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0001058	ORPHA:465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0001685	ORPHA:465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:465	Congenital plasminogen activator inhibitor type 1 deficiency		HP:0005261	ORPHA:465	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001263	ORPHA:79329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001999	ORPHA:79329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0003655	ORPHA:79329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000253	ORPHA:79329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001250	ORPHA:79329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001252	ORPHA:79329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001508	ORPHA:79329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000194	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000268	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000316	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000358	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000363	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000358	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000395	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000444	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000494	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000527	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000678	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000767	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000818	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0000938	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001007	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001156	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001290	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001627	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001629	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001643	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001789	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001892	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001929	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0001965	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0002020	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0002098	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0002521	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0002557	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0002578	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0002650	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0002808	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0003186	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0003347	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0003540	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0004313	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0004315	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0005387	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0009765	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0010990	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0011471	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0011675	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0011968	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0012171	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0012444	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0012469	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0031381	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0200117	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG		HP:0500173	ORPHA:79329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG	NOT	HP:0001321	ORPHA:79329	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79329	MGAT2-CDG	NOT	HP:0009830	ORPHA:79329	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001250	ORPHA:505237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0010864	ORPHA:505237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000218	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000219	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000248	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000252	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000276	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000278	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000343	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000365	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000369	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000400	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000426	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000445	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000470	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000494	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000527	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000637	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000960	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001182	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001187	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001263	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001290	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001344	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001508	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001511	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001762	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001845	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0002119	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0002540	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0002553	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0002650	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0003121	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0004322	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0004325	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0005469	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0007370	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0011304	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0011968	ORPHA:505237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000028	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0000729	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001166	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001251	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001257	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001276	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001629	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001631	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0001770	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0002120	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0002510	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0008772	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0012450	ORPHA:505237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505237	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome		HP:0100021	ORPHA:505237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000939	ORPHA:231222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0010972	ORPHA:231222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0011904	ORPHA:231222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0025066	ORPHA:231222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000924	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000952	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000980	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001978	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0002659	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0004349	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0011031	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0012132	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0045048	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0100724	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0200042	ORPHA:231222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000114	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000938	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001081	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001392	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001410	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001433	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001626	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001722	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001744	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001974	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0002092	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0002240	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0012465	ORPHA:231222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000135	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000819	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000821	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000829	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0000846	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001394	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0001402	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231222	Beta-thalassemia intermedia		HP:0002176	ORPHA:231222	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001511	ORPHA:1708	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001518	ORPHA:1708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001622	ORPHA:1708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001627	ORPHA:1708	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0100602	ORPHA:1708	TAS		HP:0040282			H	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000047	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000085	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000119	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000750	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000765	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001159	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001195	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001263	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001629	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001631	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001643	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0002011	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0002089	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0004484	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0006267	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0009800	ORPHA:1708	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0011024	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0011471	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0030084	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0100555	ORPHA:1708	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000154	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000365	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000366	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0000954	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001250	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001545	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0001680	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0002088	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0002245	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0003319	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0005587	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0005773	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0009778	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0011470	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0011640	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0012372	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0031703	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1708	Mosaic trisomy 16 syndrome		HP:0100864	ORPHA:1708	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0000958	ORPHA:461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0000962	ORPHA:461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0000966	ORPHA:461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0008064	ORPHA:461	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0007018	ORPHA:461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0007759	ORPHA:461	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0000028	ORPHA:461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0000717	ORPHA:461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0001270	ORPHA:461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0002167	ORPHA:461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0007549	ORPHA:461	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:461	Recessive X-linked ichthyosis		HP:0001249	ORPHA:461	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000028	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000218	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000340	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000343	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000347	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000426	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000494	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000767	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001166	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001249	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001387	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0002714	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0100490	ORPHA:1707	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000055	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000252	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000324	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000470	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000508	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000581	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001250	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001252	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001276	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0005988	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0030680	ORPHA:1707	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000098	ORPHA:1707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0000383	ORPHA:1707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001511	ORPHA:1707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0001539	ORPHA:1707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1707	Distal duplication 15q syndrome		HP:0002023	ORPHA:1707	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0011904	ORPHA:231226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0011905	ORPHA:231226	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000980	ORPHA:231226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001971	ORPHA:231226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001978	ORPHA:231226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0004840	ORPHA:231226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0011273	ORPHA:231226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0025066	ORPHA:231226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0025547	ORPHA:231226	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000164	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000737	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000819	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000821	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000823	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000829	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000939	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000952	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000953	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001394	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001395	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001433	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001510	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001531	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001744	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001954	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0002014	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0002094	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0002829	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0002857	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0004936	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0006487	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0009004	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0011031	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0011842	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0011968	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0031035	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0040075	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0200042	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0200123	ORPHA:231226	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000582	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0000846	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001402	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001644	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0001722	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0002007	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0005280	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0010620	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0011675	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231226	Dominant beta-thalassemia		HP:0430028	ORPHA:231226	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000028	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000268	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000311	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000325	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000347	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000358	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000426	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000463	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000470	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000474	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000670	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0001263	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0003196	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0004622	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0006482	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0010720	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0100543	ORPHA:1716	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000218	ORPHA:1716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0001166	ORPHA:1716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0007477	ORPHA:1716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0007598	ORPHA:1716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0008736	ORPHA:1716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0030680	ORPHA:1716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0100490	ORPHA:1716	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000055	ORPHA:1716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000453	ORPHA:1716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000612	ORPHA:1716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0000767	ORPHA:1716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0001176	ORPHA:1716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0004097	ORPHA:1716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1716	Distal duplication 18q syndrome		HP:0004209	ORPHA:1716	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000278	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000445	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000527	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001007	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001250	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001999	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002720	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002850	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0003241	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0004313	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0008947	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0012745	ORPHA:79330	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000034	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000218	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000269	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000407	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000648	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000649	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000821	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0000969	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001332	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001433	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001561	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001596	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001631	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001640	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001712	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0001873	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002079	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002098	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002104	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002240	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002286	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002791	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0002943	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0004315	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0004463	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0007430	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0010557	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0012450	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0020110	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0031218	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0040288	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79330	MOGS-CDG		HP:0100598	ORPHA:79330	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000233	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000340	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000377	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000384	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000430	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000431	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000506	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000581	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000582	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000601	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0001256	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0002021	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0002553	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0002591	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0007018	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0008689	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0011800	ORPHA:1715	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000160	ORPHA:1715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0001167	ORPHA:1715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0001760	ORPHA:1715	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000252	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0000347	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0001319	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0001511	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0002705	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0004322	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0010628	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1715	Trisomy 18p syndrome		HP:0030680	ORPHA:1715	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0003236	ORPHA:79332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0008947	ORPHA:79332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0012301	ORPHA:79332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0012379	ORPHA:79332	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000369	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000431	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000545	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001976	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001999	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0002910	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0003256	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0003563	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0003645	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0004855	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0005543	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0008936	ORPHA:79332	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000219	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000238	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000316	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000343	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000821	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0000969	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001305	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001321	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001518	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001622	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001744	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0001892	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0002014	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0002240	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0003186	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0005989	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0011003	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79332	B4GALT1-CDG		HP:0011123	ORPHA:79332	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000600	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000717	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0001252	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0001256	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0001260	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0001263	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0001508	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0002381	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0002474	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0002916	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0007018	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0010529	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0010535	ORPHA:1713	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000325	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000337	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000347	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000494	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000739	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0002020	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0002353	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0002650	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0007010	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0008499	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0011098	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0030680	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0200136	ORPHA:1713	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000154	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000252	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000316	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000365	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0000358	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0002079	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0004322	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0006482	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1713	17p11.2 microduplication syndrome		HP:0010807	ORPHA:1713	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0000364	ORPHA:457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0000457	ORPHA:457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0000518	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0000656	ORPHA:457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0000962	ORPHA:457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0001019	ORPHA:457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0001161	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0001376	ORPHA:457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0001645	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0001829	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0001944	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0002047	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0002093	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0002205	ORPHA:457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0007431	ORPHA:457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0008064	ORPHA:457	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0012472	ORPHA:457	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457	Harlequin ichthyosis		HP:0100716	ORPHA:457	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001873	ORPHA:54057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001923	ORPHA:54057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001937	ORPHA:54057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0002094	ORPHA:54057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0003324	ORPHA:54057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001250	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001259	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001289	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001297	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0002014	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0002027	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0002315	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0045040	ORPHA:54057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0000083	ORPHA:54057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0000093	ORPHA:54057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0000707	ORPHA:54057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0000790	ORPHA:54057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001658	ORPHA:54057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001945	ORPHA:54057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0011675	ORPHA:54057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0001919	ORPHA:54057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:54057	Thrombotic thrombocytopenic purpura		HP:0012101	ORPHA:54057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001252	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001508	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001954	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0002719	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0002910	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0008897	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0011968	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0012301	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0012444	ORPHA:79333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0000077	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0000253	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0000952	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001167	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001250	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001265	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001284	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001518	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001627	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001999	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0002014	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0002240	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0003236	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0007392	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0011451	ORPHA:79333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0000160	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0000278	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0000347	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0000470	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001181	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001272	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0001433	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0012157	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79333	COG7-CDG		HP:0100807	ORPHA:79333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0000218	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0000347	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0000470	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0004322	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0001513	ORPHA:314795	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0001773	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0002650	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0002857	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0002967	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0002982	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0009821	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0003067	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0009816	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0003712	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0005856	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:314795	SHOX-related short stature		HP:0005974	ORPHA:314795	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0000252	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0000308	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0000316	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0000365	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0000750	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001195	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001249	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001250	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001252	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001263	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001321	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001511	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0001629	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0007018	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0008897	ORPHA:1711	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0000023	ORPHA:1711	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0000476	ORPHA:1711	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0002119	ORPHA:1711	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0002650	ORPHA:1711	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1711	Mosaic trisomy 17 syndrome		HP:0100559	ORPHA:1711	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0001581	ORPHA:499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0001596	ORPHA:499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0001945	ORPHA:499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0002076	ORPHA:499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0002716	ORPHA:499	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0003326	ORPHA:499	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0011123	ORPHA:499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499	Kerion celsi		HP:0100838	ORPHA:499	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000218	ORPHA:79318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000486	ORPHA:79318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000582	ORPHA:79318	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000154	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000219	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000276	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000278	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000286	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000303	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000316	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000343	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000448	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000463	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000565	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000750	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000938	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000939	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001250	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001263	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001265	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001321	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001382	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001763	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001999	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002013	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002751	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0003186	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0007552	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0008936	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0009125	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0011220	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0011968	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0012448	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0100807	ORPHA:79318	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000044	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000091	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000093	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000100	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000377	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000400	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000426	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000510	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000518	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000545	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000842	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000845	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000855	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000870	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001249	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001251	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001320	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001395	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001508	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001698	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001929	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001945	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001976	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002098	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002280	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002828	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002910	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002925	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0003073	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0005562	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0008734	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0009830	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0010463	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0011443	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0011842	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0011858	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0011951	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0012509	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0012882	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0030146	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0030609	ORPHA:79318	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0000926	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001004	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001305	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001639	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001681	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0001701	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002170	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0002625	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0012050	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0031404	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79318	PMM2-CDG		HP:0040238	ORPHA:79318	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:493	Familial keratoacanthoma		HP:0000962	ORPHA:493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:493	Familial keratoacanthoma		HP:0001482	ORPHA:493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:493	Familial keratoacanthoma		HP:0002664	ORPHA:493	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:493	Familial keratoacanthoma		HP:0009720	ORPHA:493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:493	Familial keratoacanthoma		HP:0012740	ORPHA:493	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:493	Familial keratoacanthoma		HP:0200034	ORPHA:493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:493	Familial keratoacanthoma		HP:0200042	ORPHA:493	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0012379	ORPHA:79319	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0001395	ORPHA:79319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0002014	ORPHA:79319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0002240	ORPHA:79319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0003073	ORPHA:79319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0003256	ORPHA:79319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0040246	ORPHA:79319	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0000825	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0000969	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0001409	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0001410	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0001508	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0001929	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0001977	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0002013	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0002239	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0002243	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0004855	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0005543	ORPHA:79319	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG		HP:0000821	ORPHA:79319	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG	NOT	HP:0000707	ORPHA:79319	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79319	MPI-CDG	NOT	HP:0001249	ORPHA:79319	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:492	Proliferating trichilemmal cyst		HP:0002209	ORPHA:492	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:492	Proliferating trichilemmal cyst		HP:0200040	ORPHA:492	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:492	Proliferating trichilemmal cyst		HP:0200042	ORPHA:492	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0007447	ORPHA:495	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0000218	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0001041	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0001072	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0001795	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0001810	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0005406	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0007404	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0007556	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0008391	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0010765	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0011370	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0012785	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0030318	ORPHA:495	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0001805	ORPHA:495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0009775	ORPHA:495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0025474	ORPHA:495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:495	Transgrediens et progrediens palmoplantar keratoderma		HP:0031452	ORPHA:495	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0000044	ORPHA:494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0000175	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0000365	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0000407	ORPHA:494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0000962	ORPHA:494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0001596	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0001597	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0002143	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0002797	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0007460	ORPHA:494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0007465	ORPHA:494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0008064	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0008388	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0009775	ORPHA:494	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0100543	ORPHA:494	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0100716	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:494	Keratoderma hereditarium mutilans		HP:0200034	ORPHA:494	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0001249	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0001257	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0001258	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0001263	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0001310	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0002495	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0003487	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0007256	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0008944	ORPHA:459056	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0000483	ORPHA:459056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0000540	ORPHA:459056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0000639	ORPHA:459056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0001265	ORPHA:459056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0001290	ORPHA:459056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0012511	ORPHA:459056	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459056	Autosomal recessive spastic paraplegia type 75		HP:0030187	ORPHA:459056	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1706	Mosaic trisomy 15 syndrome		HP:0000707	ORPHA:1706	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1706	Mosaic trisomy 15 syndrome		HP:0001155	ORPHA:1706	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1706	Mosaic trisomy 15 syndrome		HP:0001252	ORPHA:1706	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1706	Mosaic trisomy 15 syndrome		HP:0002916	ORPHA:1706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1706	Mosaic trisomy 15 syndrome		HP:0004097	ORPHA:1706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1706	Mosaic trisomy 15 syndrome		HP:0100490	ORPHA:1706	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0000365	ORPHA:1705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0000501	ORPHA:1705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0001643	ORPHA:1705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0001679	ORPHA:1705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0002101	ORPHA:1705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0002916	ORPHA:1705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0004322	ORPHA:1705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0007370	ORPHA:1705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0010935	ORPHA:1705	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1705	Distal duplication 14q syndrome		HP:0100543	ORPHA:1705	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0012379	ORPHA:79320	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000707	ORPHA:79320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001250	ORPHA:79320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001251	ORPHA:79320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001252	ORPHA:79320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001508	ORPHA:79320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0011968	ORPHA:79320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0012758	ORPHA:79320	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000158	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000316	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000369	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000486	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000924	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000952	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001392	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001929	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001999	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0002243	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0002650	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0002652	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0003073	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0003256	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0003642	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0004855	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0005543	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0006118	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0040246	ORPHA:79320	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000510	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0000546	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001156	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0001321	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0002625	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0003563	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0008373	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79320	ALG6-CDG		HP:0030348	ORPHA:79320	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000154	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000218	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000347	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000426	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000431	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000470	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0001249	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0001263	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0001508	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0002007	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0002916	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0030680	ORPHA:1703	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000028	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000047	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000175	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000316	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000358	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000463	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000581	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000774	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0001250	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0004397	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0007598	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0008551	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0008736	ORPHA:1703	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000508	ORPHA:1703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0000772	ORPHA:1703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0008056	ORPHA:1703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0100490	ORPHA:1703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1703	Mosaic trisomy 14 syndrome		HP:0100559	ORPHA:1703	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0012379	ORPHA:79321	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001252	ORPHA:79321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001263	ORPHA:79321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0002060	ORPHA:79321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0002719	ORPHA:79321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0011024	ORPHA:79321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0011968	ORPHA:79321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000119	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000252	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000365	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000366	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000377	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000478	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000818	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000938	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001250	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001410	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0002086	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0002813	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0030680	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0040064	ORPHA:79321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001276	ORPHA:79321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001285	ORPHA:79321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001332	ORPHA:79321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001871	ORPHA:79321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0003186	ORPHA:79321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0012444	ORPHA:79321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0045005	ORPHA:79321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000158	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000172	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000218	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000518	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0000639	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001010	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001305	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0001638	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0002079	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0002089	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0002804	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0005871	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0009125	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0012110	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0012157	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0012305	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79321	ALG3-CDG		HP:0012762	ORPHA:79321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000028	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000164	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000218	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000232	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000233	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000243	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000252	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000343	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000347	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000499	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000574	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000601	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000664	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0000774	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0001028	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0001162	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0001166	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0001231	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0001800	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0002916	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0003196	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0006610	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0008056	ORPHA:1702	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0009738	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0009906	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0100543	ORPHA:1702	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1702	Non-distal duplication 13q syndrome		HP:0100790	ORPHA:1702	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001250	ORPHA:79322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0003236	ORPHA:79322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0005484	ORPHA:79322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0008947	ORPHA:79322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0012758	ORPHA:79322	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000316	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001508	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001976	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002705	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002910	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0004855	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0005543	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0012448	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0100321	ORPHA:79322	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000243	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000293	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000319	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000347	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000486	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000488	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000494	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000565	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000639	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0000648	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001251	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001257	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001272	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001298	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001395	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001397	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001433	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001847	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0001852	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002014	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002057	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002059	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002119	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002123	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002164	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0002240	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0003186	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0003241	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0003560	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0005280	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0005469	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0006380	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0006879	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0007333	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0009826	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0009830	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0010804	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0010806	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0010818	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0010819	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0011152	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0011471	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0012385	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0025404	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79322	DPM1-CDG		HP:0100704	ORPHA:79322	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0003642	ORPHA:79323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0010864	ORPHA:79323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0012379	ORPHA:79323	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0008947	ORPHA:79323	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0000233	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0000242	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0000260	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0000648	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0000803	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0000824	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0000964	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0001250	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0001276	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0002119	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0002521	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0003236	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0005478	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0007965	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0008064	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0008529	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0011968	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0012704	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0025474	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0030353	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0040189	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79323	MPDU1-CDG		HP:0040288	ORPHA:79323	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001622	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001762	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001792	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001852	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001873	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001988	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001999	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002020	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002079	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002119	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002162	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002389	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002650	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002910	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0003026	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0003049	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0003073	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0003146	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0004209	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0009623	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0010557	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0011327	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0011344	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0011471	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0011800	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0011849	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0012385	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0012448	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0012766	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0030353	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0100807	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0410240	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0410243	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0410263	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0410295	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0410305	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000969	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001561	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001643	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001655	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002566	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002902	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0003186	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0009124	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0011623	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0100806	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0200128	ORPHA:79324	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0012379	ORPHA:79324	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000119	ORPHA:79324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0003256	ORPHA:79324	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000253	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000750	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000759	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001249	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001252	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001508	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001929	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002011	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002194	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002205	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0002257	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0003645	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0004855	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0005543	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0006532	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0008151	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0010976	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0011968	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0040246	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0100776	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0410018	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0410242	ORPHA:79324	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000028	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000047	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000054	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000219	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000276	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000286	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000322	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000347	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000377	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000407	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000426	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000445	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000478	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000486	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0000541	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001250	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001290	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001302	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001321	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001511	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79324	ALG12-CDG		HP:0001582	ORPHA:79324	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000707	ORPHA:79325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001252	ORPHA:79325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001999	ORPHA:79325	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000478	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000518	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000969	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001250	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001263	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001541	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001622	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001789	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001873	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002902	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002910	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0003256	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0003642	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0011024	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0011121	ORPHA:79325	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000158	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000316	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000369	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000488	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000639	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000648	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0000973	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001001	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001156	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001251	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001508	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001511	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001518	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001562	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001762	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001903	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001929	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0001976	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002013	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002014	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002079	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002119	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002120	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002352	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0002415	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0003186	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0005543	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0011968	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0012385	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79325	ALG8-CDG		HP:0100678	ORPHA:79325	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0001891	ORPHA:54028	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0002015	ORPHA:54028	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0004840	ORPHA:54028	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0012343	ORPHA:54028	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0100594	ORPHA:54028	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0000206	ORPHA:54028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0000980	ORPHA:54028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0003388	ORPHA:54028	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0000160	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0001598	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0002027	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0004396	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0010284	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0012473	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0025062	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:54028	Plummer-Vinson syndrome		HP:0100825	ORPHA:54028	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001875	ORPHA:486	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0002718	ORPHA:486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0004429	ORPHA:486	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0000155	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0000230	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0000704	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001581	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001888	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001945	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0002014	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0002027	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0002090	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0004798	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0005425	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0011107	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0012311	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0012384	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0025439	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0410018	ORPHA:486	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0000938	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001028	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001880	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001909	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0001915	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0002863	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0003453	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0004808	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0006480	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0006721	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0025452	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:486	Autosomal dominant severe congenital neutropenia		HP:0100658	ORPHA:486	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0008271	ORPHA:485	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000311	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000520	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0001367	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0001387	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0001591	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0002663	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003037	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003330	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003498	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0005280	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0007773	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0007964	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0011003	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0012069	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0012785	ORPHA:485	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000175	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000365	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000541	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000926	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000947	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003016	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003026	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003040	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003051	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003311	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003521	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0007992	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0008063	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0009815	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0010306	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0010574	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0010580	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0010646	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0012230	ORPHA:485	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000201	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000470	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000518	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0001488	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0002949	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0003417	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0004557	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0006375	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0006454	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0008422	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0012019	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0025474	ORPHA:485	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0000256	ORPHA:485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0002086	ORPHA:485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0002176	ORPHA:485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:485	Kniest dysplasia		HP:0008755	ORPHA:485	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0000790	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0001945	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0001974	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0002027	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0011227	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0012085	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0025143	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0025615	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0032169	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0100518	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0100525	ORPHA:488	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0002586	ORPHA:488	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0002664	ORPHA:488	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0010766	ORPHA:488	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0010783	ORPHA:488	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:488	Urachal cyst		HP:0031500	ORPHA:488	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000365	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000407	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000505	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000708	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000763	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001172	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001251	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001257	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001263	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001939	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002676	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0003457	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0009830	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0010318	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0011968	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0034322	ORPHA:487	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000737	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001250	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001288	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001508	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001945	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002013	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002123	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002205	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002313	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002376	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0003134	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0004374	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0033031	ORPHA:487	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000020	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000618	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0000648	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001188	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001265	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001324	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001336	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001761	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001824	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002179	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002312	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0001288	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002359	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002421	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002445	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002878	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0002922	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0025013	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0030211	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0100639	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:487	Krabbe disease		HP:0100963	ORPHA:487	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:482	Kimura disease		HP:0001880	ORPHA:482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:482	Kimura disease		HP:0002729	ORPHA:482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:482	Kimura disease		HP:0003212	ORPHA:482	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:482	Kimura disease		HP:0002716	ORPHA:482	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:482	Kimura disease		HP:0010286	ORPHA:482	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0000029	ORPHA:481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0000144	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0000771	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0001252	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0001260	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0001265	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0001288	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0001618	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0003119	ORPHA:481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0003202	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0005978	ORPHA:481	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0100022	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:481	Kennedy disease		HP:0100639	ORPHA:481	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000580	ORPHA:480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000590	ORPHA:480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001709	ORPHA:480	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000365	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000508	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000830	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001251	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001252	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001315	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0002922	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0003200	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0003202	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0003457	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0004622	ORPHA:480	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000467	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000726	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000819	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000823	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0000829	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001324	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001337	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001638	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0001947	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0002015	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0002750	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0003546	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0004322	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0004374	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0012622	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:480	Kearns-Sayre syndrome		HP:0100543	ORPHA:480	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0000217	ORPHA:43393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0001315	ORPHA:43393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0003403	ORPHA:43393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0009073	ORPHA:43393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0012332	ORPHA:43393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0030000	ORPHA:43393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0030209	ORPHA:43393	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0000315	ORPHA:43393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0000802	ORPHA:43393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0002019	ORPHA:43393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0002483	ORPHA:43393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0030357	ORPHA:43393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:5000027	ORPHA:43393	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0000966	ORPHA:43393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0001097	ORPHA:43393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:43393	Lambert-Eaton myasthenic syndrome		HP:0004926	ORPHA:43393	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:42062	Iminoglycinuria		HP:0003080	ORPHA:42062	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:42062	Iminoglycinuria		HP:0003108	ORPHA:42062	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:42062	Iminoglycinuria		HP:0003137	ORPHA:42062	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:42062	Iminoglycinuria	NOT	HP:0002154	ORPHA:42062	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:42062	Iminoglycinuria	NOT	HP:0003260	ORPHA:42062	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:42062	Iminoglycinuria	NOT	HP:0008358	ORPHA:42062	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0000365	ORPHA:438134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0000613	ORPHA:438134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0000992	ORPHA:438134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0001263	ORPHA:438134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0002066	ORPHA:438134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0002180	ORPHA:438134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0100585	ORPHA:438134	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0001256	ORPHA:438134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0004322	ORPHA:438134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0007763	ORPHA:438134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0031087	ORPHA:438134	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0000252	ORPHA:438134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0000776	ORPHA:438134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0001272	ORPHA:438134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0002664	ORPHA:438134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:438134	PCNA-related progressive neurodegenerative photosensitivity syndrome		HP:0010864	ORPHA:438134	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0000853	ORPHA:566243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0001649	ORPHA:566243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0033075	ORPHA:566243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0033077	ORPHA:566243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0000403	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0000739	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0000752	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0001328	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0002750	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0007018	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0011788	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0025379	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0032069	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0034288	ORPHA:566243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0000407	ORPHA:566243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0001530	ORPHA:566243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0001962	ORPHA:566243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0012758	ORPHA:566243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta		HP:0025484	ORPHA:566243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:566243	Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta	NOT	HP:0031098	ORPHA:566243	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0000973	ORPHA:33111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0001582	ORPHA:33111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0002665	ORPHA:33111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0010783	ORPHA:33111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0012189	ORPHA:33111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0030053	ORPHA:33111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0000121	ORPHA:33111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0001919	ORPHA:33111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0002733	ORPHA:33111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33111	Granulomatous slack skin		HP:0003072	ORPHA:33111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0000718	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001252	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001298	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001324	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001508	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001533	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002059	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002133	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002151	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002167	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002169	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002194	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002353	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0003535	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0007204	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0010864	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0011925	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0031936	ORPHA:505216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0000020	ORPHA:505216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0000648	ORPHA:505216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001250	ORPHA:505216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001257	ORPHA:505216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001344	ORPHA:505216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0001347	ORPHA:505216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:505216	3-methylglutaconic aciduria type 9		HP:0002521	ORPHA:505216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001263	ORPHA:459061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001999	ORPHA:459061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0002209	ORPHA:459061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0004322	ORPHA:459061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0011220	ORPHA:459061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0045075	ORPHA:459061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000077	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000238	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000243	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001305	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001320	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001763	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001800	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0005280	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0007291	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0012385	ORPHA:459061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000023	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000175	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000248	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000286	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000316	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000347	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000369	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000494	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000687	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000739	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0000805	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001250	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001274	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001631	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001650	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0001970	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0004442	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0004482	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0007018	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0007598	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0010535	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0012712	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0030799	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		HP:0200055	ORPHA:459061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000044	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000054	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000144	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000458	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000823	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000830	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0003164	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0004409	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0008734	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0008736	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0100639	ORPHA:478	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000028	ORPHA:478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001608	ORPHA:478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0003187	ORPHA:478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0004349	ORPHA:478	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000008	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000104	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000175	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000407	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000505	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000508	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000551	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000639	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000771	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0000786	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001250	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001251	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001252	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001260	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001288	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001324	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001335	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001337	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001513	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001761	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0001763	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0002652	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0002750	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0002757	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0008064	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0009804	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0010550	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0030016	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:478	Kallmann syndrome		HP:0030680	ORPHA:478	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0000083	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0000648	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001249	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001250	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001252	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001254	ORPHA:79312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001259	ORPHA:79312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001260	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001263	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001266	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001297	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001332	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001508	ORPHA:79312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001638	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001733	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001744	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001873	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001875	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001903	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001944	ORPHA:79312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0001987	ORPHA:79312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0002017	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0002027	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0002039	ORPHA:79312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0002098	ORPHA:79312	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0002240	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0002721	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0011968	ORPHA:79312	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79312	Vitamin B12-unresponsive methylmalonic acidemia type mut-		HP:0100022	ORPHA:79312	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0000121	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0000790	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0003110	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0003159	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0008672	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0012211	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0012531	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0100515	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93600	Primary hyperoxaluria type 3		HP:0100518	ORPHA:93600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000218	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000246	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000286	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000316	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000389	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000509	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000988	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0001287	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0001369	ORPHA:33110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0001508	ORPHA:33110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0001581	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0001875	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0001944	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0001945	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0002014	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0002024	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0002110	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0002205	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0002719	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0002721	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0002754	ORPHA:33110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0004432	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0000377	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0012115	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0012378	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0012735	ORPHA:33110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0100658	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0100806	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33110	Autosomal non-syndromic agammaglobulinemia		HP:0200043	ORPHA:33110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0001250	ORPHA:79314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0002383	ORPHA:79314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0001249	ORPHA:79314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0010864	ORPHA:79314	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0000256	ORPHA:79314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0000708	ORPHA:79314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0001252	ORPHA:79314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0001285	ORPHA:79314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0002071	ORPHA:79314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0004375	ORPHA:79314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0007360	ORPHA:79314	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79314	L-2-hydroxyglutaric aciduria		HP:0002381	ORPHA:79314	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0000975	ORPHA:94093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001945	ORPHA:94093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002300	ORPHA:94093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0004372	ORPHA:94093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0007076	ORPHA:94093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0012332	ORPHA:94093	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0000822	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001337	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001649	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001942	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001974	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002015	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002307	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0003236	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0003394	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0003781	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0012378	ORPHA:94093	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0000020	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0000093	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0000713	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0000739	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001259	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001298	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001894	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001919	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001944	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002013	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002018	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002072	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002149	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002153	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002204	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002615	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002901	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002902	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002905	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002910	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002913	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002917	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0003155	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0003201	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0003228	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0010553	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0011675	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0011951	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0025145	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0025435	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0031258	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0040288	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0100735	ORPHA:94093	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001662	ORPHA:94093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0001873	ORPHA:94093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0002045	ORPHA:94093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94093	Neuroleptic malignant syndrome		HP:0100806	ORPHA:94093	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000028	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000044	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000054	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000118	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000134	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000786	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000802	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0001608	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0002231	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0002750	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0003187	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0003782	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0006610	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0008187	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0008197	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0008734	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0011961	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0030019	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0040171	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000002	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000013	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000716	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000739	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000771	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000823	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000869	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000938	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000939	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0008724	ORPHA:432	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000164	ORPHA:432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000175	ORPHA:432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000316	ORPHA:432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0002761	ORPHA:432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0005280	ORPHA:432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0008527	ORPHA:432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0012385	ORPHA:432	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000026	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:432	Normosmic congenital hypogonadotropic hypogonadism		HP:0000027	ORPHA:432	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0100267	ORPHA:141291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0000271	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0001611	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0002793	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0005105	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0005216	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0005324	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0009088	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0410011	ORPHA:141291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0000419	ORPHA:141291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0000668	ORPHA:141291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:141291	Cleft lip and alveolus		HP:0002015	ORPHA:141291	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0000842	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0001263	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0001513	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0002591	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0002615	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0005307	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0012332	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0100503	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0100543	ORPHA:369873	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0002354	ORPHA:369873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0007018	ORPHA:369873	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0000729	ORPHA:369873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency		HP:0001952	ORPHA:369873	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency	NOT	HP:0001252	ORPHA:369873	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency	NOT	HP:0004322	ORPHA:369873	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency	NOT	HP:0011968	ORPHA:369873	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:369873	Obesity due to SIM1 deficiency	NOT	HP:0012339	ORPHA:369873	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0030083	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0100651	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0004860	ORPHA:85138	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0008720	ORPHA:85138	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0100522	ORPHA:85138	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002014	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002017	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002019	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002027	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002039	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002615	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002960	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0003154	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0012378	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000127	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000848	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001649	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001897	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001944	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002149	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002153	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002902	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0004319	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0005976	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0008226	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0012364	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0008163	ORPHA:85138	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0008207	ORPHA:85138	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000953	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001324	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001508	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001824	ORPHA:85138	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0025406	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0033834	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0034055	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0034061	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0034071	ORPHA:85138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000823	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000829	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000835	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000872	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0000958	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001045	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001250	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001278	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001596	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0001943	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002215	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002321	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002608	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0002829	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0003072	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0006462	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0008209	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0010512	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85138	Addison disease		HP:0030018	ORPHA:85138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0000852	ORPHA:94090	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0002901	ORPHA:94090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0002905	ORPHA:94090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0003165	ORPHA:94090	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0002199	ORPHA:94090	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0001657	ORPHA:94090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0003394	ORPHA:94090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0003401	ORPHA:94090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0003472	ORPHA:94090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0003739	ORPHA:94090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0011458	ORPHA:94090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2		HP:0012049	ORPHA:94090	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2	NOT	HP:0003456	ORPHA:94090	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2	NOT	HP:0003761	ORPHA:94090	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2	NOT	HP:0010766	ORPHA:94090	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:94090	Pseudohypoparathyroidism type 2	NOT	HP:0030057	ORPHA:94090	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0000944	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0000969	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0000988	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0000989	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0001061	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0001369	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0001824	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0001903	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0001945	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0002037	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0002633	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0002650	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0002653	ORPHA:324964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0002754	ORPHA:324964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0002797	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0003468	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0003565	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0003765	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0004396	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0005464	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0005930	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0006824	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0011227	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0012378	ORPHA:324964	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0100774	ORPHA:324964	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0100781	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:324964	Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis		HP:0100847	ORPHA:324964	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000121	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000648	ORPHA:428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000708	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000712	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000716	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000739	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000958	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0000964	ORPHA:428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0001231	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0001596	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0001597	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0001635	ORPHA:428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002027	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002150	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002356	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002516	ORPHA:428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002615	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002793	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002901	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002905	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0002917	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0003401	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0003457	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0003473	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0004349	ORPHA:428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0004372	ORPHA:428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0007400	ORPHA:428	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0011675	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0012608	ORPHA:428	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:428	Autosomal dominant hypocalcemia		HP:0040148	ORPHA:428	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0000127	ORPHA:427	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0000848	ORPHA:427	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0000846	ORPHA:427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0001508	ORPHA:427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0002153	ORPHA:427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0002615	ORPHA:427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0002902	ORPHA:427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0004319	ORPHA:427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0011106	ORPHA:427	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0001254	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0001278	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0001510	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0001942	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0001954	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0002014	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0002017	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0002049	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0011968	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:427	Familial hypoaldosteronism		HP:0012364	ORPHA:427	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0000508	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0000737	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0000750	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001251	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001252	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001254	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001270	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001300	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001336	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001348	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001761	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001762	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002019	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002063	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002066	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002067	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002071	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002174	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002375	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002395	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002451	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0003487	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0003781	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0003785	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0004373	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0010553	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0011968	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0030166	ORPHA:101150	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001256	ORPHA:101150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001945	ORPHA:101150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0007325	ORPHA:101150	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0001290	ORPHA:101150	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101150	Autosomal recessive dopa-responsive dystonia		HP:0002448	ORPHA:101150	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0003149	ORPHA:94088	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0003537	ORPHA:94088	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0030973	ORPHA:94088	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0000091	ORPHA:94088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0001919	ORPHA:94088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0008651	ORPHA:94088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0012211	ORPHA:94088	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0000790	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0002013	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0002018	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0002150	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0003138	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0003418	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0012213	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0012595	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94088	Hereditary renal hypouricemia		HP:0012622	ORPHA:94088	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0000256	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0000944	ORPHA:429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0001156	ORPHA:429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0001249	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0001831	ORPHA:429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0002644	ORPHA:429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0002650	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0002652	ORPHA:429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0002758	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0002823	ORPHA:429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0002970	ORPHA:429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0002983	ORPHA:429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0003307	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0003312	ORPHA:429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0003416	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0001382	ORPHA:429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0006487	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0009811	ORPHA:429	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0010535	ORPHA:429	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:429	Hypochondroplasia		HP:0011405	ORPHA:429	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000852	ORPHA:94089	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0002901	ORPHA:94089	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0002905	ORPHA:94089	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003165	ORPHA:94089	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003456	ORPHA:94089	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000293	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000311	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000470	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000518	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000639	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000684	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0004322	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0005280	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0006297	ORPHA:94089	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000509	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000716	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000737	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000739	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0001265	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0001657	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0002094	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003034	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003394	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003401	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003472	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003739	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0003909	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0005700	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0011001	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0011458	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0012049	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0100660	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0100749	ORPHA:94089	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0000824	ORPHA:94089	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0002199	ORPHA:94089	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B		HP:0008227	ORPHA:94089	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B	NOT	HP:0003761	ORPHA:94089	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B	NOT	HP:0010766	ORPHA:94089	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:94089	Pseudohypoparathyroidism type 1B	NOT	HP:0030057	ORPHA:94089	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0000836	ORPHA:424	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0011790	ORPHA:424	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0000853	ORPHA:424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0001518	ORPHA:424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0001824	ORPHA:424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0002014	ORPHA:424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0002378	ORPHA:424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0008249	ORPHA:424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0011784	ORPHA:424	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0000713	ORPHA:424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0000752	ORPHA:424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0001263	ORPHA:424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0001270	ORPHA:424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0002360	ORPHA:424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor		HP:0005616	ORPHA:424	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor	NOT	HP:0012372	ORPHA:424	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:424	Familial hyperthyroidism due to mutations in TSH receptor	NOT	HP:0030057	ORPHA:424	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000028	ORPHA:99776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000085	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000110	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000126	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000130	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000175	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000218	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000239	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000252	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000269	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000316	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000347	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000369	ORPHA:99776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000414	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000465	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000470	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000476	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000568	ORPHA:99776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000582	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0000601	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001195	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001249	ORPHA:99776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001263	ORPHA:99776	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001305	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001376	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001511	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001561	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001562	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001629	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001631	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001643	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001651	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001654	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001706	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001746	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001762	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001789	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001792	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001838	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0001869	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002006	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002101	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002119	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002414	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002566	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002650	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002652	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002827	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002937	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0002983	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0003042	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0004422	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0005562	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0005815	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0006191	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0007957	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0008736	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0011027	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0012815	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0040019	ORPHA:99776	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0100490	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99776	Mosaic trisomy 9 syndrome		HP:0100752	ORPHA:99776	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0001942	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0001945	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0002047	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0002789	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0002905	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0003552	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0004755	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0004756	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0011964	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0012416	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0031320	ORPHA:423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0001722	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0001919	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0002153	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0002913	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0003256	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0006554	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0006682	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0008331	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0008942	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0008978	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:0009045	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:423	Malignant hyperthermia of anesthesia		HP:3000005	ORPHA:423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0002621	ORPHA:425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0003119	ORPHA:425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0003233	ORPHA:425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0007759	ORPHA:425	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0000622	ORPHA:425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0000991	ORPHA:425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0001114	ORPHA:425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0001681	ORPHA:425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:425	Apolipoprotein A-I deficiency		HP:0005181	ORPHA:425	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99771	Bifid uvula		HP:0000193	ORPHA:99771	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99771	Bifid uvula		HP:0008376	ORPHA:99771	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99771	Bifid uvula		HP:0011819	ORPHA:99771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99771	Bifid uvula		HP:0410030	ORPHA:99771	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0000325	ORPHA:94083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0001249	ORPHA:94083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0002451	ORPHA:94083	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0000053	ORPHA:94083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0001256	ORPHA:94083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0001260	ORPHA:94083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0001288	ORPHA:94083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0002061	ORPHA:94083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0002342	ORPHA:94083	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0000750	ORPHA:94083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0001250	ORPHA:94083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0002353	ORPHA:94083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94083	Partington syndrome		HP:0007380	ORPHA:94083	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0000185	ORPHA:99772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0000220	ORPHA:99772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0002033	ORPHA:99772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0010863	ORPHA:99772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0011469	ORPHA:99772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0200136	ORPHA:99772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0000327	ORPHA:99772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0000403	ORPHA:99772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0000405	ORPHA:99772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0001611	ORPHA:99772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0009088	ORPHA:99772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0011219	ORPHA:99772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99772	Cleft velum		HP:0011951	ORPHA:99772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0002092	ORPHA:422	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0002094	ORPHA:422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0011025	ORPHA:422	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0001279	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0001962	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0002240	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0005133	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0005180	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0012378	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0030148	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0030848	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0100749	ORPHA:422	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:422	Idiopathic/heritable pulmonary arterial hypertension		HP:0010741	ORPHA:422	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0002668	ORPHA:94080	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001069	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001095	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001342	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001618	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001824	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001962	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0002018	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0002331	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0002574	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0002640	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0002864	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0003072	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0003345	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0003574	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0003639	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0008629	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0010532	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0011703	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0011979	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0012378	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0031284	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0100749	ORPHA:94080	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0000405	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0000790	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0000980	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001293	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001337	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001605	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0001635	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94080	Non-functioning paraganglioma		HP:0025269	ORPHA:94080	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0040317	ORPHA:94086	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0000121	ORPHA:94086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0002014	ORPHA:94086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0003072	ORPHA:94086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0004324	ORPHA:94086	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0001942	ORPHA:94086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0001988	ORPHA:94086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0002905	ORPHA:94086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0002910	ORPHA:94086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0002925	ORPHA:94086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0031507	ORPHA:94086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94086	Blue diaper syndrome		HP:0031883	ORPHA:94086	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000529	ORPHA:85128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000551	ORPHA:85128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0001123	ORPHA:85128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0030469	ORPHA:85128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0030474	ORPHA:85128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0030618	ORPHA:85128	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000493	ORPHA:85128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000539	ORPHA:85128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000546	ORPHA:85128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000580	ORPHA:85128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000608	ORPHA:85128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0007814	ORPHA:85128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0032118	ORPHA:85128	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000510	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000603	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000610	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0000662	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0001129	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0007722	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0007984	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0030528	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy		HP:0030529	ORPHA:85128	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85128	Bothnia retinal dystrophy	NOT	HP:0007737	ORPHA:85128	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001249	ORPHA:457260	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000252	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000504	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000718	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000729	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000752	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001257	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001290	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0002136	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0100660	ORPHA:457260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000202	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000365	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000505	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0000826	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001000	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001250	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001263	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001382	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0001999	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0002079	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0002119	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0002539	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457260	X-linked intellectual disability-hypotonia-movement disorder syndrome		HP:0002650	ORPHA:457260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0000774	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0000944	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0002240	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0002757	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0100530	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0000820	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0001252	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0001744	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0003355	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:417	Neonatal severe primary hyperparathyroidism		HP:0004322	ORPHA:417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0003159	ORPHA:416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0008672	ORPHA:416	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0000121	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0000164	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0000488	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0000543	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0000648	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0000790	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0001508	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0001942	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0002653	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0002757	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0002910	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0004417	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0005789	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0006479	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0007663	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0009830	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0011072	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0011506	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0012072	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0012622	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0012722	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0025324	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0030880	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0031981	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0100758	ORPHA:416	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0001063	ORPHA:416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0002150	ORPHA:416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0003774	ORPHA:416	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0000965	ORPHA:416	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0001638	ORPHA:416	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:416	Primary hyperoxaluria		HP:0025520	ORPHA:416	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:419	Hyperprolinemia type 1		HP:0000093	ORPHA:419	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:419	Hyperprolinemia type 1		HP:0000112	ORPHA:419	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:419	Hyperprolinemia type 1		HP:0001250	ORPHA:419	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:419	Hyperprolinemia type 1		HP:0003137	ORPHA:419	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:419	Hyperprolinemia type 1		HP:0008358	ORPHA:419	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:419	Hyperprolinemia type 1		HP:0100753	ORPHA:419	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0000951	ORPHA:412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0002155	ORPHA:412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0003124	ORPHA:412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0003141	ORPHA:412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0003233	ORPHA:412	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0000660	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0000819	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001013	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001084	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001114	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001397	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001513	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0002240	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0002635	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0010874	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0025530	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0031290	ORPHA:412	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0000799	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0000821	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001681	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001735	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0001997	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0004943	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0004950	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0005181	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:412	Dysbetalipoproteinemia		HP:0012397	ORPHA:412	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001347	ORPHA:415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001987	ORPHA:415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0011965	ORPHA:415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0012026	ORPHA:415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0012758	ORPHA:415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0100543	ORPHA:415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001249	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001254	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001258	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001289	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001290	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001328	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001410	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001508	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002038	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002073	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002120	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002169	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002240	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002311	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002495	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002572	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002789	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002910	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0003218	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0006846	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0007256	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0011098	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0011968	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0012115	ORPHA:415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001250	ORPHA:415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001259	ORPHA:415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001950	ORPHA:415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002064	ORPHA:415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0002123	ORPHA:415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0003256	ORPHA:415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0007052	ORPHA:415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0000533	ORPHA:415	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0001399	ORPHA:415	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:415	Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome		HP:0040030	ORPHA:415	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0001302	ORPHA:572013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0007360	ORPHA:572013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0008936	ORPHA:572013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0010864	ORPHA:572013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0012758	ORPHA:572013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0025100	ORPHA:572013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0030301	ORPHA:572013	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0000486	ORPHA:572013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0002015	ORPHA:572013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0004305	ORPHA:572013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0033725	ORPHA:572013	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0000011	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0000324	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0000609	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0000733	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0001257	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0002827	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0012469	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0032794	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:572013	Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome		HP:0100704	ORPHA:572013	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0000529	ORPHA:414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0000533	ORPHA:414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0000545	ORPHA:414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0012026	ORPHA:414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0200065	ORPHA:414	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0000518	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0000523	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0000618	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0001103	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0001133	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0003355	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0007675	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0040031	ORPHA:414	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0000365	ORPHA:414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0001250	ORPHA:414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:414	Gyrate atrophy of choroid and retina		HP:0001595	ORPHA:414	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0000028	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0000062	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0000252	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0000347	ORPHA:452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0000966	ORPHA:452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001249	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001250	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001252	ORPHA:452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001257	ORPHA:452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001263	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001274	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001302	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001522	ORPHA:452	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001629	ORPHA:452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001643	ORPHA:452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0001738	ORPHA:452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0002024	ORPHA:452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0002119	ORPHA:452	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0002251	ORPHA:452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0008736	ORPHA:452	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:452	X-linked lissencephaly with abnormal genitalia		HP:0011220	ORPHA:452	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284400	Small cell carcinoma of the bladder		HP:0000790	ORPHA:284400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284400	Small cell carcinoma of the bladder		HP:0002027	ORPHA:284400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284400	Small cell carcinoma of the bladder		HP:0003072	ORPHA:284400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284400	Small cell carcinoma of the bladder		HP:0009725	ORPHA:284400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284400	Small cell carcinoma of the bladder		HP:0100518	ORPHA:284400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284400	Small cell carcinoma of the bladder		HP:0000010	ORPHA:284400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:455	Superficial epidermolytic ichthyosis		HP:0000963	ORPHA:455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:455	Superficial epidermolytic ichthyosis		HP:0000969	ORPHA:455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:455	Superficial epidermolytic ichthyosis		HP:0000982	ORPHA:455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:455	Superficial epidermolytic ichthyosis		HP:0008064	ORPHA:455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:455	Superficial epidermolytic ichthyosis		HP:0008066	ORPHA:455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:455	Superficial epidermolytic ichthyosis		HP:0100792	ORPHA:455	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:455	Superficial epidermolytic ichthyosis		HP:0010783	ORPHA:455	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0000083	ORPHA:454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0000958	ORPHA:454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0000962	ORPHA:454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0000982	ORPHA:454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0000989	ORPHA:454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0001581	ORPHA:454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0002664	ORPHA:454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0002665	ORPHA:454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0002960	ORPHA:454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0006775	ORPHA:454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0008064	ORPHA:454	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0010783	ORPHA:454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0100242	ORPHA:454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0100326	ORPHA:454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:454	Acquired ichthyosis		HP:0200034	ORPHA:454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85112	Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome		HP:0000982	ORPHA:85112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85112	Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome		HP:0006739	ORPHA:85112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85112	Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome		HP:0012245	ORPHA:85112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0011098	ORPHA:240112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0006977	ORPHA:240112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0030391	ORPHA:240112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0001268	ORPHA:240112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002465	ORPHA:240112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002549	ORPHA:240112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0009088	ORPHA:240112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0031434	ORPHA:240112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0007158	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0000511	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002527	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0000741	ORPHA:240112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0030784	ORPHA:240112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0025268	ORPHA:240112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0001300	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002312	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002015	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002172	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002381	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0030217	ORPHA:240112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240112	Progressive supranuclear palsy-progressive non-fluent aphasia syndrome		HP:0002167	ORPHA:240112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0001510	ORPHA:94068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002650	ORPHA:94068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002938	ORPHA:94068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0003521	ORPHA:94068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0010575	ORPHA:94068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0045060	ORPHA:94068	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000280	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000470	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000926	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000939	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002808	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002857	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0003180	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0009824	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0012368	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0030838	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0040194	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0100569	ORPHA:94068	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000162	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000175	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000316	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000347	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000365	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000541	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0000545	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0001270	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0001552	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0001760	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002176	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002515	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002795	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0002996	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0003026	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0003097	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0003306	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0003418	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0004349	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0008462	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0008755	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0010585	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0030839	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94068	Spondyloepiphyseal dysplasia congenita		HP:0100864	ORPHA:94068	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0000175	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0000272	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0000303	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0000322	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0001250	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0001252	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0001357	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0001629	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0001800	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0002714	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0009835	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0000316	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0002553	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0004397	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0010185	ORPHA:94066	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94066	Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia		HP:0010864	ORPHA:94066	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000750	ORPHA:369891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001263	ORPHA:369891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001270	ORPHA:369891	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000154	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000158	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000194	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000369	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000414	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000431	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000582	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000708	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000729	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001252	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001328	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0002342	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0002465	ORPHA:369891	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000028	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000218	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000248	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000286	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000294	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000303	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000311	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000316	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000325	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000337	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000341	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000365	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000384	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000400	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000470	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000508	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000540	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000545	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000687	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000711	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000713	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000717	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000718	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0000752	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001155	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001159	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001251	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001357	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001537	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001627	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001629	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001655	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0001760	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0002236	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0002311	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0002313	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0002353	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0002714	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0003196	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0004322	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0005280	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0005612	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0007633	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0007700	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0010841	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0011228	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0011800	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0012385	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0030084	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369891	Developmental delay-facial dysmorphism syndrome due to MED13L deficiency		HP:0100025	ORPHA:369891	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0000347	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0000448	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0000463	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0000581	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0001943	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0002612	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0003281	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0003452	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0006579	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0006709	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:446	Neonatal hemochromatosis		HP:0100542	ORPHA:446	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0030272	ORPHA:447	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001878	ORPHA:447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001903	ORPHA:447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0003641	ORPHA:447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0025406	ORPHA:447	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001907	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001923	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0002094	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0002315	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0002574	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0002625	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0003138	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0004936	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0008282	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0012543	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0012622	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0020181	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0025435	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0032106	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0032147	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0040303	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0100749	ORPHA:447	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0000083	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0000093	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0000802	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0000822	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0000952	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001254	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001297	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001658	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001873	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001876	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001882	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001919	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0002204	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0002639	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0004420	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0012132	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0030248	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0032043	ORPHA:447	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0001994	ORPHA:447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0002015	ORPHA:447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0003076	ORPHA:447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:447	Paroxysmal nocturnal hemoglobinuria		HP:0025271	ORPHA:447	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0000970	ORPHA:441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0001278	ORPHA:441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0012099	ORPHA:441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0012332	ORPHA:441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0025142	ORPHA:441	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0000020	ORPHA:441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0001279	ORPHA:441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0002019	ORPHA:441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0100518	ORPHA:441	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:441	Pure autonomic failure		HP:0000802	ORPHA:441	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0001300	ORPHA:99750	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0000496	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0000597	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0000643	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0000657	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0000726	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0001268	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0002063	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0002067	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0002317	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0002527	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0002751	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0005329	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0007076	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0009088	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0010526	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0011098	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0025330	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0031825	ORPHA:99750	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0000719	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0001260	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0001337	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0004302	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0004373	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0006801	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0006977	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0007256	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99750	Atypical progressive supranuclear palsy syndrome		HP:0010522	ORPHA:99750	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:444	Marie Unna hereditary hypotrichosis		HP:0001596	ORPHA:444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444	Marie Unna hereditary hypotrichosis		HP:0002208	ORPHA:444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444	Marie Unna hereditary hypotrichosis		HP:0002209	ORPHA:444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444	Marie Unna hereditary hypotrichosis		HP:0100840	ORPHA:444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:444	Marie Unna hereditary hypotrichosis		HP:0200102	ORPHA:444	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94064	Deafness-infertility syndrome		HP:0000027	ORPHA:94064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94064	Deafness-infertility syndrome		HP:0000407	ORPHA:94064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94064	Deafness-infertility syndrome		HP:0003251	ORPHA:94064	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001531	ORPHA:284417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0002154	ORPHA:284417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0008872	ORPHA:284417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0011451	ORPHA:284417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0012279	ORPHA:284417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0012736	ORPHA:284417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0030215	ORPHA:284417	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0000474	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001250	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001276	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001347	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001511	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0002079	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0008936	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0012430	ORPHA:284417	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0000316	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0000340	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0000347	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0000470	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001285	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001320	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001336	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001339	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001363	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0001776	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0002392	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0003121	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0005280	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0006380	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0006466	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0006956	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0007704	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0008064	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0009879	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0011097	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0011196	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0011471	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0012448	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0040288	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		HP:0200048	ORPHA:284417	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000179	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000252	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000276	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000316	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000324	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000365	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000426	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000486	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000589	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000639	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000776	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000824	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001172	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001508	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001513	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001627	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001780	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0002023	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0002650	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0002808	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0005280	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0009623	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0011100	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0011968	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0012810	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0030084	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0030260	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0100790	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0200055	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0002475	ORPHA:94065	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001263	ORPHA:94065	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000286	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000319	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000343	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000356	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000494	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000708	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001156	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001249	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001252	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001382	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0001518	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0002719	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0004322	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0008897	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0009890	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0011229	ORPHA:94065	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000028	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000047	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000160	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000164	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94065	15q24 microdeletion syndrome		HP:0000174	ORPHA:94065	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000085	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000086	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000089	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000233	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000252	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000316	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000325	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000347	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000426	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000445	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000490	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000574	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000664	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000668	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000750	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000819	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0000953	ORPHA:94063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001252	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001256	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001263	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001328	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001337	ORPHA:94063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001482	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001508	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001511	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0001743	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0002007	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0002308	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0002566	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0002650	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0002714	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0003202	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0003396	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0004209	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0004322	ORPHA:94063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0005288	ORPHA:94063	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94063	12q14 microdeletion syndrome		HP:0010739	ORPHA:94063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000218	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000708	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000750	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0001252	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0001256	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0001337	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0002342	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0004322	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0025502	ORPHA:457240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000054	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000252	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000316	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000337	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000348	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000400	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000486	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000639	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000716	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000729	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000733	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000739	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000742	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000824	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0000954	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0001250	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0001288	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0001385	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0001658	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0002069	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0002171	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0002206	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0002487	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0004437	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0006986	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0007033	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0008734	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457240	X-linked intellectual disability-short stature-overweight syndrome		HP:0010864	ORPHA:457240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002186	ORPHA:240103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0003474	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0007158	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002067	ORPHA:240103	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0000514	ORPHA:240103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002172	ORPHA:240103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002063	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002359	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002098	ORPHA:240103	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002015	ORPHA:240103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002374	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0001260	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002354	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0000511	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002381	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0009088	ORPHA:240103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0004373	ORPHA:240103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0001337	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome	NOT	HP:0000743	ORPHA:240103	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0007256	ORPHA:240103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0030217	ORPHA:240103	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0045084	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0004305	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0007885	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0006961	ORPHA:240103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0001188	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0000570	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0001268	ORPHA:240103	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0000751	ORPHA:240103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:240103	Progressive supranuclear palsy-corticobasal syndrome		HP:0002548	ORPHA:240103	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0005180	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0012378	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0030718	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0031664	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0001635	ORPHA:439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0001640	ORPHA:439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0005150	ORPHA:439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0010741	ORPHA:439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0000961	ORPHA:439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0001694	ORPHA:439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0002094	ORPHA:439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0012418	ORPHA:439	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0001217	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0001631	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0001655	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0001708	ORPHA:439	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0011623	ORPHA:439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0011712	ORPHA:439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:439	Isolated right ventricular hypoplasia		HP:0012383	ORPHA:439	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000501	ORPHA:94058	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000572	ORPHA:94058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0011497	ORPHA:94058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0012636	ORPHA:94058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000488	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000553	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000587	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000613	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0007906	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0020166	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0030532	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0200026	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:3000032	ORPHA:94058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000593	ORPHA:94058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0004329	ORPHA:94058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0007850	ORPHA:94058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0012040	ORPHA:94058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0025358	ORPHA:94058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0030953	ORPHA:94058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94058	Neovascular glaucoma		HP:0000541	ORPHA:94058	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99748	Pontiac fever		HP:0001945	ORPHA:99748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99748	Pontiac fever		HP:0002315	ORPHA:99748	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99748	Pontiac fever		HP:0003326	ORPHA:99748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99748	Pontiac fever		HP:0012378	ORPHA:99748	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99748	Pontiac fever		HP:0012735	ORPHA:99748	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0000185	ORPHA:99742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0000252	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0000340	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0000347	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0000648	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0000737	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0000939	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001252	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001274	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001320	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001339	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001376	ORPHA:99742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001522	ORPHA:99742	TAS		HP:0040281			C	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001558	ORPHA:99742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001942	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0001992	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0002069	ORPHA:99742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0002119	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0002240	ORPHA:99742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0002414	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0002509	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0004331	ORPHA:99742	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0005968	ORPHA:99742	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0011344	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99742	Amish lethal microcephaly		HP:0011968	ORPHA:99742	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0000958	ORPHA:94059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0000989	ORPHA:94059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0003138	ORPHA:94059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0012622	ORPHA:94059	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0002360	ORPHA:94059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0003774	ORPHA:94059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0011112	ORPHA:94059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0011354	ORPHA:94059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0031355	ORPHA:94059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0031901	ORPHA:94059	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0000716	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0001581	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0002918	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0003072	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0008732	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0011123	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0100725	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:94059	Uremic pruritus		HP:0200034	ORPHA:94059	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0000164	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0000239	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0000737	ORPHA:436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0000772	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0000774	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0000944	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0001024	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0001250	ORPHA:436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0001252	ORPHA:436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0001363	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0001531	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0001903	ORPHA:436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0002093	ORPHA:436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0002097	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0002757	ORPHA:436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0003072	ORPHA:436	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0004322	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0006487	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0008872	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:436	Hypophosphatasia		HP:0010781	ORPHA:436	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0000421	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0000988	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001251	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001254	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001259	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001276	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001337	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001347	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001695	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001744	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0001945	ORPHA:99745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002014	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002019	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002027	ORPHA:99745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002239	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002240	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002315	ORPHA:99745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002383	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0002829	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0003326	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0004936	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0006530	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0011675	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0012378	ORPHA:99745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0012733	ORPHA:99745	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0012735	ORPHA:99745	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99745	Typhoid		HP:0100785	ORPHA:99745	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001249	ORPHA:171929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001510	ORPHA:171929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001511	ORPHA:171929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001518	ORPHA:171929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000119	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000159	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000268	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000316	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000348	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000366	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000478	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000598	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000924	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001155	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001250	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001760	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001999	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0011220	ORPHA:171929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000077	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000143	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000202	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000218	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000233	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000278	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000286	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000347	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000358	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000369	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000400	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000463	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000494	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0000582	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001290	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001305	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001384	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001627	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001762	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0001831	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0002007	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0002015	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0002020	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0002033	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0002266	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0002311	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0002937	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0003196	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0003199	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0005280	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0005562	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0006055	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0006958	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0009600	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0009879	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0010537	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0010851	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0011181	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0011193	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0011344	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0011451	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0011467	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0012385	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0012745	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171929	Trisomy 10p syndrome		HP:0012794	ORPHA:171929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0001260	ORPHA:101110	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0001272	ORPHA:101110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0001618	ORPHA:101110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0002067	ORPHA:101110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0002514	ORPHA:101110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0007338	ORPHA:101110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0012049	ORPHA:101110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0030188	ORPHA:101110	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0000640	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0001251	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0001347	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0002066	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0002321	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0007256	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0007351	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0010545	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0030185	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0030186	ORPHA:101110	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101110	Spinocerebellar ataxia type 20		HP:0002080	ORPHA:101110	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0007328	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0007663	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0011468	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0031422	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0100275	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0000317	ORPHA:101111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002013	ORPHA:101111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002574	ORPHA:101111	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002073	ORPHA:101111	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0000012	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0000486	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0000639	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0000763	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0001761	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002066	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002464	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002522	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002650	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0002936	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0003387	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0003445	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0003487	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101111	Spinocerebellar ataxia type 25		HP:0006937	ORPHA:101111	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0001787	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0003388	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0003738	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0008305	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0008331	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0009045	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0011356	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0025474	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0025526	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0025528	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0040189	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0200039	ORPHA:284426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0001036	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0001919	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0002046	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0002910	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0003072	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0007432	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0012622	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0031190	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0031236	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0045040	ORPHA:284426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284426	Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency		HP:0000989	ORPHA:284426	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0001151	ORPHA:101112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0001260	ORPHA:101112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0002070	ORPHA:101112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0002073	ORPHA:101112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0007240	ORPHA:101112	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0000639	ORPHA:101112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0000641	ORPHA:101112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0001272	ORPHA:101112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0002078	ORPHA:101112	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0003487	ORPHA:101112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26		HP:0007034	ORPHA:101112	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26	NOT	HP:0001250	ORPHA:101112	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26	NOT	HP:0002380	ORPHA:101112	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26	NOT	HP:0003470	ORPHA:101112	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:101112	Spinocerebellar ataxia type 26	NOT	HP:0003474	ORPHA:101112	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0000867	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0000965	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0001939	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0002905	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0003207	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0003774	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0011122	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0011986	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0100658	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0100758	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0100806	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0200042	ORPHA:280062	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280062	Calciphylaxis		HP:0033260	ORPHA:280062	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0001250	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0001263	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0001274	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0001338	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0002059	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0002119	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0004330	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0006824	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0009830	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0012444	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0012447	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0025517	ORPHA:85179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0000405	ORPHA:85179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0002090	ORPHA:85179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85179	Infantile osteopetrosis with neuroaxonal dysplasia		HP:0025116	ORPHA:85179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000248	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000341	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000343	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000348	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000486	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000639	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000938	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001252	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0003100	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0005280	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0010864	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0011842	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0100704	ORPHA:369837	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000079	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000121	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000365	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000431	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000540	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000767	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001627	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002069	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002123	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002150	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002650	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002705	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002714	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002750	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0003072	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0003282	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0008676	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0009824	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0010818	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0012373	ORPHA:369837	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000107	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000110	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000272	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000347	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000369	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000483	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000545	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000582	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000826	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0000829	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001272	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001363	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001382	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001513	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001631	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001643	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0001723	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002020	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002101	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002121	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002155	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002263	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002283	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002720	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002850	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0002870	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0003186	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0006480	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0006961	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0010536	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0010804	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0010841	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0010850	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0011199	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0011470	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0012718	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0025330	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369837	Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome		HP:0030856	ORPHA:369837	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0002652	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0002753	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0002834	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0002982	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0002986	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0003022	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0003031	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0003856	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0003871	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0003874	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0003985	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0003986	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0004026	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0005622	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0006387	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0006413	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0006429	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0008783	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0008804	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0010498	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0010502	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0010540	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0010639	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0011001	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0032208	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0100670	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0100916	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0100917	ORPHA:85188	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0000938	ORPHA:85188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0002650	ORPHA:85188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85188	Metaphyseal dysplasia, Braun-Tinschert type		HP:0006323	ORPHA:85188	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000218	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000242	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000256	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000260	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000272	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000347	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000494	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000520	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000885	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000938	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0000940	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0001248	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0001760	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0002212	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0002645	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0002673	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0002703	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0002753	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0005446	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0006391	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0006429	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0008438	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0009911	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0010539	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0011001	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85184	Craniometadiaphyseal dysplasia, wormian bone type		HP:0011220	ORPHA:85184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0001123	ORPHA:499096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0007641	ORPHA:499096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0030857	ORPHA:499096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0032036	ORPHA:499096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0200026	ORPHA:499096	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0000572	ORPHA:499096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0000603	ORPHA:499096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0001085	ORPHA:499096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0002315	ORPHA:499096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0200057	ORPHA:499096	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis		HP:0030786	ORPHA:499096	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499096	Isolated optic neuritis	NOT	HP:0033342	ORPHA:499096	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0200026	ORPHA:293381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0009926	ORPHA:293381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0000613	ORPHA:293381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0001131	ORPHA:293381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0000622	ORPHA:293381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0008039	ORPHA:293381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0000495	ORPHA:293381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0000559	ORPHA:293381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0000529	ORPHA:293381	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0031792	ORPHA:293381	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:293381	Epithelial recurrent erosion dystrophy		HP:0001097	ORPHA:293381	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0012760	ORPHA:280071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001249	ORPHA:280071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001250	ORPHA:280071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001263	ORPHA:280071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0003160	ORPHA:280071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0003642	ORPHA:280071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0008947	ORPHA:280071	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000252	ORPHA:280071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000365	ORPHA:280071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000504	ORPHA:280071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001276	ORPHA:280071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001347	ORPHA:280071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001999	ORPHA:280071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0011968	ORPHA:280071	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000278	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000343	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000348	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000486	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0000958	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001251	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0001508	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002059	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002179	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002282	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002375	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002500	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002509	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002572	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002650	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0002910	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0003186	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0005968	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0008000	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0008936	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0009124	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0010851	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0011842	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0012448	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0012704	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280071	ALG11-CDG		HP:0012762	ORPHA:280071	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000505	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000548	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000926	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0001156	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0002812	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0002979	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0003015	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0003025	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0003026	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0003300	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0003510	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0005054	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0005930	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0006487	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0007703	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0008905	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0009803	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0010049	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0010583	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0030329	ORPHA:85167	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000539	ORPHA:85167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000887	ORPHA:85167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000946	ORPHA:85167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0003375	ORPHA:85167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0031171	ORPHA:85167	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000486	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000568	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000589	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000602	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0000639	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0001105	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0001132	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0002650	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0007401	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0007688	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0007957	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0009918	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome		HP:0012153	ORPHA:85167	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85167	Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome	NOT	HP:0001249	ORPHA:85167	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:85168	Craniofacial conodysplasia		HP:0000238	ORPHA:85168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85168	Craniofacial conodysplasia		HP:0000271	ORPHA:85168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85168	Craniofacial conodysplasia		HP:0002176	ORPHA:85168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85168	Craniofacial conodysplasia		HP:0004439	ORPHA:85168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85168	Craniofacial conodysplasia		HP:0010230	ORPHA:85168	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85169	Familial digital arthropathy-brachydactyly		HP:0001156	ORPHA:85169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85169	Familial digital arthropathy-brachydactyly		HP:0004268	ORPHA:85169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85169	Familial digital arthropathy-brachydactyly		HP:0005793	ORPHA:85169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85169	Familial digital arthropathy-brachydactyly		HP:0005819	ORPHA:85169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85169	Familial digital arthropathy-brachydactyly		HP:0006239	ORPHA:85169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85169	Familial digital arthropathy-brachydactyly		HP:0009882	ORPHA:85169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0001347	ORPHA:101108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0002066	ORPHA:101108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0002070	ORPHA:101108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0002073	ORPHA:101108	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0000514	ORPHA:101108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0001260	ORPHA:101108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0001310	ORPHA:101108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0003487	ORPHA:101108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0006886	ORPHA:101108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101108	Spinocerebellar ataxia type 23		HP:0010831	ORPHA:101108	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0001260	ORPHA:101109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0002066	ORPHA:101109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0002070	ORPHA:101109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0002395	ORPHA:101109	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0000508	ORPHA:101109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0000514	ORPHA:101109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0000597	ORPHA:101109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0000639	ORPHA:101109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0003487	ORPHA:101109	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0001300	ORPHA:101109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0030186	ORPHA:101109	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0000708	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0000716	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0001257	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0001332	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0002063	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0002346	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0002354	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0002451	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:101109	Spinocerebellar ataxia type 28		HP:0100543	ORPHA:101109	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0000272	ORPHA:85174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0000926	ORPHA:85174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0001762	ORPHA:85174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0002650	ORPHA:85174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0003042	ORPHA:85174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0006243	ORPHA:85174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0008905	ORPHA:85174	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0001539	ORPHA:85174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85174	Pseudodiastrophic dysplasia		HP:0030680	ORPHA:85174	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85175	Astley-Kendall dysplasia		HP:0002703	ORPHA:85175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85175	Astley-Kendall dysplasia		HP:0002983	ORPHA:85175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85175	Astley-Kendall dysplasia		HP:0008873	ORPHA:85175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85175	Astley-Kendall dysplasia		HP:0010655	ORPHA:85175	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0002652	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0002827	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0002868	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0002990	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0003027	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0004018	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0004322	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0006413	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0006434	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0006487	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0006633	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0008808	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0010508	ORPHA:85170	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0001249	ORPHA:85170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85170	Mesomelic dysplasia, Savarirayan type		HP:0003042	ORPHA:85170	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0000252	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0000272	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0000444	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0000446	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0000518	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0000520	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0000926	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0001762	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0002007	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0003311	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0004279	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0004322	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0004582	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0010230	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0011833	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85172	Microcephalic osteodysplastic dysplasia, Saul-Wilson type		HP:0200055	ORPHA:85172	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0000028	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0000047	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0000078	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0000126	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0000135	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0000369	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0000835	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0001252	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0001511	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0002007	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0002983	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0005280	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85173	IMAGe syndrome		HP:0100255	ORPHA:85173	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000219	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000316	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000324	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000430	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000431	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000445	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000456	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0001155	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0001511	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0002714	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0002817	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0004209	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0007874	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0010939	ORPHA:521308	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0000453	ORPHA:521308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0001274	ORPHA:521308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0001631	ORPHA:521308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0001763	ORPHA:521308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0007330	ORPHA:521308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0008115	ORPHA:521308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome		HP:0012165	ORPHA:521308	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521308	Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome	NOT	HP:0001249	ORPHA:521308	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002719	ORPHA:331235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0032169	ORPHA:331235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0001047	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0001510	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0200043	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0030880	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002850	ORPHA:331235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002205	ORPHA:331235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0012432	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0000491	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency	NOT	HP:0002720	ORPHA:331235	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency	NOT	HP:0004315	ORPHA:331235	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0011109	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0000010	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002110	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0032261	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0032262	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002960	ORPHA:331235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0000872	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002725	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0001370	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0001973	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0001904	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0003493	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0012204	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0100658	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002840	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0005353	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0000388	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0025439	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0031691	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0030757	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0033430	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0011370	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0007499	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0100537	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002837	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0031292	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0032275	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0012203	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0009098	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002028	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0032170	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0012393	ORPHA:331235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0003193	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002099	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0031047	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0006775	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0012539	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002890	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0012126	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0045080	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0032218	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0005415	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0030380	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0032140	ORPHA:331235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0100280	ORPHA:331235	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002788	ORPHA:331235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0006532	ORPHA:331235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0011108	ORPHA:331235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0002716	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0004798	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0001287	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:331235	Selective IgM deficiency		HP:0100806	ORPHA:331235	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0000969	ORPHA:263665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0005523	ORPHA:263665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0100828	ORPHA:263665	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002027	ORPHA:263665	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002014	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002019	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002020	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002253	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002573	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002588	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0002592	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0004295	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0005266	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:263665	NK-cell enteropathy		HP:0012425	ORPHA:263665	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0000023	ORPHA:2196	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0000112	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0000545	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0000567	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0000639	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0000787	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0000790	ORPHA:2196	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0001116	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0001537	ORPHA:2196	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0007703	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2196	Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement		HP:0100530	ORPHA:2196	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000256	ORPHA:457279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000750	ORPHA:457279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001263	ORPHA:457279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001290	ORPHA:457279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001319	ORPHA:457279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0031936	ORPHA:457279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000478	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000718	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000729	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000733	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000744	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001344	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001999	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002317	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002342	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002465	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002650	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0010864	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0025160	ORPHA:457279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000276	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000325	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000369	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000486	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000494	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001251	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001273	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001627	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001629	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002389	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002500	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0003196	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0006956	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0011220	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0011800	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0100702	ORPHA:457279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000176	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000218	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000219	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000260	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000268	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000324	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000343	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0000483	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001137	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001250	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001284	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001357	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001374	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001583	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001631	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001647	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001655	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0001943	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002007	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002021	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002028	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0002558	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0005216	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0005988	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0011937	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457279	Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome		HP:0100350	ORPHA:457279	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001410	ORPHA:565782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002013	ORPHA:565782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002027	ORPHA:565782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002910	ORPHA:565782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0000083	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0000155	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001250	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001289	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001394	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001596	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001733	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001882	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001889	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0001945	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002018	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002239	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002315	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002321	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0002329	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0006515	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0012378	ORPHA:565782	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:565782	Methotrexate toxicity		HP:0000509	ORPHA:565782	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:85163	Hypomyelination-congenital cataract syndrome		HP:0000519	ORPHA:85163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85163	Hypomyelination-congenital cataract syndrome		HP:0001263	ORPHA:85163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85163	Hypomyelination-congenital cataract syndrome		HP:0001317	ORPHA:85163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85163	Hypomyelination-congenital cataract syndrome		HP:0002342	ORPHA:85163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85163	Hypomyelination-congenital cataract syndrome		HP:0006808	ORPHA:85163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85163	Hypomyelination-congenital cataract syndrome		HP:0007256	ORPHA:85163	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85164	Camptodactyly-tall stature-scoliosis-hearing loss syndrome		HP:0000365	ORPHA:85164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85164	Camptodactyly-tall stature-scoliosis-hearing loss syndrome		HP:0002650	ORPHA:85164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85164	Camptodactyly-tall stature-scoliosis-hearing loss syndrome		HP:0100490	ORPHA:85164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85164	Camptodactyly-tall stature-scoliosis-hearing loss syndrome		HP:0100491	ORPHA:85164	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0000252	ORPHA:85165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0000889	ORPHA:85165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0000956	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0002079	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0002197	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0002980	ORPHA:85165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0002982	ORPHA:85165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0005871	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0009118	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0010502	ORPHA:85165	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0010864	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0011344	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0012081	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85165	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome		HP:0012444	ORPHA:85165	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0000774	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0000926	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0001191	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0001773	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0002652	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0002983	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0003021	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0003090	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0003270	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0004279	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0006487	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0008839	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0008873	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0009882	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0010306	ORPHA:85166	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0000272	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0000369	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0000882	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0001561	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0001789	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0002089	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0002970	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0005280	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0011220	ORPHA:85166	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:85166	Platyspondylic dysplasia, Torrance type		HP:0000175	ORPHA:85166	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:409	Hyperkeratosis lenticularis perstans		HP:0000989	ORPHA:409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:409	Hyperkeratosis lenticularis perstans		HP:0002671	ORPHA:409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:409	Hyperkeratosis lenticularis perstans		HP:0002860	ORPHA:409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:409	Hyperkeratosis lenticularis perstans		HP:0007570	ORPHA:409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:409	Hyperkeratosis lenticularis perstans		HP:0008065	ORPHA:409	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:409	Hyperkeratosis lenticularis perstans		HP:0200034	ORPHA:409	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:409	Hyperkeratosis lenticularis perstans		HP:0200042	ORPHA:409	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0000972	ORPHA:2199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0000962	ORPHA:2199	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0001217	ORPHA:2199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0001220	ORPHA:2199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0001231	ORPHA:2199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0007447	ORPHA:2199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0010765	ORPHA:2199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0025092	ORPHA:2199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0032541	ORPHA:2199	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0000975	ORPHA:2199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0008066	ORPHA:2199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0010829	ORPHA:2199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0010830	ORPHA:2199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0012385	ORPHA:2199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2199	Epidermolytic palmoplantar keratoderma		HP:0025114	ORPHA:2199	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0000982	ORPHA:2198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0002017	ORPHA:2198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0002239	ORPHA:2198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0002250	ORPHA:2198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0100751	ORPHA:2198	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0001541	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0001824	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0002015	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0002020	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0002033	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0002240	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0004396	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0025270	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0045026	ORPHA:2198	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2198	Palmoplantar keratoderma-esophageal carcinoma syndrome		HP:0100760	ORPHA:2198	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:85162	Facial onset sensory and motor neuronopathy		HP:0001260	ORPHA:85162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85162	Facial onset sensory and motor neuronopathy		HP:0001324	ORPHA:85162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85162	Facial onset sensory and motor neuronopathy		HP:0002015	ORPHA:85162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85162	Facial onset sensory and motor neuronopathy		HP:0002380	ORPHA:85162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85162	Facial onset sensory and motor neuronopathy		HP:0003202	ORPHA:85162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85162	Facial onset sensory and motor neuronopathy		HP:0003394	ORPHA:85162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:85162	Facial onset sensory and motor neuronopathy		HP:0003401	ORPHA:85162	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2197	Idiopathic hypercalciuria		HP:0002150	ORPHA:2197	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2197	Idiopathic hypercalciuria		HP:0012637	ORPHA:2197	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2197	Idiopathic hypercalciuria		HP:0000938	ORPHA:2197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2197	Idiopathic hypercalciuria		HP:0008672	ORPHA:2197	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2197	Idiopathic hypercalciuria		HP:0000939	ORPHA:2197	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2197	Idiopathic hypercalciuria	NOT	HP:0003529	ORPHA:2197	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2197	Idiopathic hypercalciuria	NOT	HP:0004363	ORPHA:2197	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0000407	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0001004	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0001873	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002167	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002488	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002878	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0003010	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0005528	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0011991	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0012378	ORPHA:228423	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0000389	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0000572	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0000587	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0000978	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0000980	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0001744	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0001824	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0001945	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002017	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002076	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002170	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002205	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002240	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002321	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0100724	ORPHA:228423	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0001974	ORPHA:228423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0002716	ORPHA:228423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228423	GATA2 deficiency spectrum		HP:0005547	ORPHA:228423	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0003072	ORPHA:405	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0003127	ORPHA:405	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0003513	ORPHA:405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0003529	ORPHA:405	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0002749	ORPHA:405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0003072	ORPHA:405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0008732	ORPHA:405	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0000934	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0002017	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0002315	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0002574	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0002918	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0004398	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0012378	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0012609	ORPHA:405	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0000787	ORPHA:405	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0001733	ORPHA:405	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0002199	ORPHA:405	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0002960	ORPHA:405	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia		HP:0012032	ORPHA:405	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:405	Familial hypocalciuric hypercalcemia	NOT	HP:0000121	ORPHA:405	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0000028	ORPHA:408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0000939	ORPHA:408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0001249	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0001250	ORPHA:408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0001252	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0001263	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0001315	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0001942	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0002167	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0002353	ORPHA:408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0002650	ORPHA:408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0003198	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0003236	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0003307	ORPHA:408	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0003457	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0004322	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:408	Isolated glycerol kinase deficiency		HP:0008182	ORPHA:408	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0001250	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0001252	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0002079	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0002154	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0002353	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0010851	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0012705	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0100247	ORPHA:407	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0001254	ORPHA:407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0002033	ORPHA:407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0002123	ORPHA:407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0005957	ORPHA:407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:407	Glycine encephalopathy		HP:0005972	ORPHA:407	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001263	ORPHA:228426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001433	ORPHA:228426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001531	ORPHA:228426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001999	ORPHA:228426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0004482	ORPHA:228426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0006528	ORPHA:228426	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000520	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000821	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001971	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0002719	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0002960	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0008947	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0011471	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0012115	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0025379	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0100646	ORPHA:228426	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000268	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000269	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000331	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000358	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000453	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0000508	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001394	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001409	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001876	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0001904	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0002007	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0002242	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0003262	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0003453	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0006554	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0011800	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0012385	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0025329	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0030084	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0030151	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0031104	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228426	Syndromic multisystem autoimmune disease due to Itch deficiency		HP:0100651	ORPHA:228426	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000677	ORPHA:99798	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0005216	ORPHA:99798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000684	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000687	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000689	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000690	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000691	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000696	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0006289	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0006336	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0011051	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0011056	ORPHA:99798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000202	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000679	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0000685	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0006297	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0006342	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0006344	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0006482	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0011053	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0011078	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0011219	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99798	Oligodontia		HP:0012472	ORPHA:99798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0000822	ORPHA:404	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0011740	ORPHA:404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0040084	ORPHA:404	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0011746	ORPHA:404	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0000360	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0000421	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0001324	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0002018	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0002170	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0002315	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0002900	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0008221	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II		HP:0200114	ORPHA:404	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:404	Familial hyperaldosteronism type II	NOT	HP:0011739	ORPHA:404	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0000822	ORPHA:403	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0011739	ORPHA:403	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0008221	ORPHA:403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0040084	ORPHA:403	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0000360	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0000421	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0001324	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0001959	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0002018	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0002170	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0002315	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0002900	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0011410	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0011746	ORPHA:403	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:403	Familial hyperaldosteronism type I		HP:0100602	ORPHA:403	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0001407	ORPHA:400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0001880	ORPHA:400	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0001824	ORPHA:400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0002611	ORPHA:400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0010702	ORPHA:400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0012378	ORPHA:400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0410019	ORPHA:400	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0000775	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0002240	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0002904	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0002910	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0003155	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0005230	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0005948	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0011458	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0025615	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0030948	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0031983	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0032101	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0032445	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0100845	ORPHA:400	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0000107	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0000138	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0000478	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0000925	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0000952	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0001025	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0001627	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0001732	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0002099	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0002585	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0003011	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0010576	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0011355	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0012062	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0012578	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0030423	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0031630	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0031700	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0045058	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:400	Cystic echinococcosis		HP:0100592	ORPHA:400	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000539	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000545	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000575	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000622	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0001123	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0001133	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0030604	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0030644	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0030786	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0200057	ORPHA:284454	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000510	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000512	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000580	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000603	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0007663	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0007722	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0007814	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0011531	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0012377	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0030662	ORPHA:284454	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000572	ORPHA:284454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0000610	ORPHA:284454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0008046	ORPHA:284454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:284454	Acute zonal occult outer retinopathy		HP:0030499	ORPHA:284454	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0000518	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0001265	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0001344	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0002240	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0001288	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0002515	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0002910	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0003198	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0003307	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0003326	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0003394	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0003560	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0003701	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0006785	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0006889	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0012762	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0040081	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0100295	ORPHA:369840	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0000252	ORPHA:369840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0001397	ORPHA:369840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0002069	ORPHA:369840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0002072	ORPHA:369840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0002078	ORPHA:369840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0008947	ORPHA:369840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18		HP:0025313	ORPHA:369840	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18	NOT	HP:0002091	ORPHA:369840	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:369840	TRAPPC11-related limb-girdle muscular dystrophy R18	NOT	HP:0005133	ORPHA:369840	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000238	ORPHA:2185	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000256	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000324	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000358	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000414	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000486	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000494	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000612	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0001249	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0001250	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0001270	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0002007	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0002119	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0002472	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0002536	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0030048	ORPHA:2185	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000407	ORPHA:2185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0000648	ORPHA:2185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0001104	ORPHA:2185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0001339	ORPHA:2185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2185	Congenital hydrocephalus		HP:0001627	ORPHA:2185	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0000079	ORPHA:2184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0000286	ORPHA:2184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0000445	ORPHA:2184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0000765	ORPHA:2184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0001334	ORPHA:2184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0001636	ORPHA:2184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0001643	ORPHA:2184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0003189	ORPHA:2184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0004299	ORPHA:2184	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2184	Hydrocephaly-low insertion umbilicus syndrome		HP:0010772	ORPHA:2184	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0000238	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0000470	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0000771	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0000815	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0001256	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0001513	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0001634	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0002162	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0002705	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0002967	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0004322	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0010044	ORPHA:2183	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0000027	ORPHA:2183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0000864	ORPHA:2183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0002550	ORPHA:2183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2183	Hydrocephalus-obesity-hypogonadism syndrome		HP:0007464	ORPHA:2183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0000238	ORPHA:2182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0000280	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0000486	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0000639	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0001181	ORPHA:2182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0001250	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0001257	ORPHA:2182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0001274	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0001331	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0001360	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0001387	ORPHA:2182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0002410	ORPHA:2182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0002516	ORPHA:2182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0004374	ORPHA:2182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2182	Hydrocephalus with stenosis of the aqueduct of Sylvius		HP:0010864	ORPHA:2182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload		HP:0003281	ORPHA:254704	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload		HP:0001808	ORPHA:254704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload		HP:0002829	ORPHA:254704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload		HP:0012378	ORPHA:254704	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload		HP:0000518	ORPHA:254704	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload	NOT	HP:0012465	ORPHA:254704	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload	NOT	HP:0040130	ORPHA:254704	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:254704	Genetic hyperferritinemia without iron overload	NOT	HP:0040135	ORPHA:254704	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0000098	ORPHA:2181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0000238	ORPHA:2181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0001166	ORPHA:2181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0001181	ORPHA:2181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0001519	ORPHA:2181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0002808	ORPHA:2181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0001382	ORPHA:2181	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0001288	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0001537	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0001659	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0002007	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0002301	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0002650	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0002705	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2181	Hydrocephaly-tall stature-joint laxity syndrome		HP:0003834	ORPHA:2181	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000238	ORPHA:2180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000303	ORPHA:2180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000912	ORPHA:2180	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000218	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000256	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000272	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000316	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000348	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000369	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000414	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000431	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000448	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000463	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000682	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000708	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000772	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000992	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0001000	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0001156	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0001249	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0001513	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0001852	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0002650	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0002937	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0003312	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0005280	ORPHA:2180	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000486	ORPHA:2180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0000545	ORPHA:2180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2180	Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome		HP:0006610	ORPHA:2180	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0000518	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0001249	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0001263	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0002072	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0002078	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0001288	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0002487	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0002650	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0003198	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0003326	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0006785	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0009020	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0009073	ORPHA:369847	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0000486	ORPHA:369847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0000545	ORPHA:369847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0001250	ORPHA:369847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0002059	ORPHA:369847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0002091	ORPHA:369847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0005133	ORPHA:369847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369847	Intellectual disability-hyperkinetic movement-truncal ataxia syndrome		HP:0008947	ORPHA:369847	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000238	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000278	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000347	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0001162	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0001274	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0001331	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0001561	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0001622	ORPHA:2189	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000175	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000176	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000193	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000358	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000369	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000490	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0001601	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0002086	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0004408	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0030680	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0030690	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0100333	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0100682	ORPHA:2189	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000028	ORPHA:2189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000528	ORPHA:2189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0000568	ORPHA:2189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0002139	ORPHA:2189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0002323	ORPHA:2189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0002983	ORPHA:2189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2189	Hydrolethalus		HP:0011027	ORPHA:2189	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001249	ORPHA:457284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001250	ORPHA:457284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000194	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000297	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000316	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001252	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001263	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001274	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001344	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001357	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0002079	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0002119	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0002465	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0002650	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0012448	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0100704	ORPHA:457284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000023	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000122	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000151	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000238	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000324	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000463	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000478	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000609	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000752	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0000767	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001382	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0001385	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0003250	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0004209	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0005487	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0006955	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0010055	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0010721	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0011471	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0012304	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0025607	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		HP:0100259	ORPHA:457284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0007166	ORPHA:53583	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0000651	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0001249	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0001258	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0001260	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0001266	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0001332	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0001347	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0002131	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0002315	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0003401	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0007256	ORPHA:53583	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:53583	Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity		HP:0002069	ORPHA:53583	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0000023	ORPHA:2295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0001374	ORPHA:2295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0002815	ORPHA:2295	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0002823	ORPHA:2295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0002999	ORPHA:2295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0003834	ORPHA:2295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0001382	ORPHA:2295	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2295	Familial articular hypermobility syndrome		HP:0009811	ORPHA:2295	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2291	Congenital velopharyngeal incompetence		HP:0000174	ORPHA:2291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2291	Congenital velopharyngeal incompetence		HP:0000220	ORPHA:2291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2291	Congenital velopharyngeal incompetence		HP:0000365	ORPHA:2291	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2291	Congenital velopharyngeal incompetence		HP:0000600	ORPHA:2291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2291	Congenital velopharyngeal incompetence		HP:0001608	ORPHA:2291	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0000121	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0000989	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0001263	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0001942	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0001944	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0002014	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0003270	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0011106	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0011472	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0011473	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2290	Microvillus inclusion disease		HP:0012211	ORPHA:2290	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0030148	ORPHA:2299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0032092	ORPHA:2299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0032554	ORPHA:2299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0000822	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0000961	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001627	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001629	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001635	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001712	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0002098	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0002789	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0008872	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0010741	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0020142	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0030973	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0031273	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0031664	ORPHA:2299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001643	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001647	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001659	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001660	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001669	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0002315	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0002875	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0004417	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0005180	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0011604	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0011712	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0031784	ORPHA:2299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001719	ORPHA:2299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0001750	ORPHA:2299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2299	Aortic arch interruption		HP:0010883	ORPHA:2299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000842	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000855	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000956	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001824	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001952	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0002725	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0002960	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003074	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003565	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0004359	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0004924	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0008283	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0011998	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0012153	ORPHA:2298	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000093	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000123	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000147	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000831	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001007	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001882	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003073	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003076	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003119	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003493	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0004323	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0004325	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0004361	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0005416	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0005978	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0008675	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0012378	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0030088	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0100879	ORPHA:2298	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000825	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0000988	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001596	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001873	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001946	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0001953	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0002090	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0002613	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0002665	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0002758	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003162	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003237	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0003261	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0004324	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0006775	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0010286	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2298	Insulin-resistance syndrome type B		HP:0012189	ORPHA:2298	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2297	Insulin-resistance syndrome type A		HP:0000823	ORPHA:2297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2297	Insulin-resistance syndrome type A		HP:0000962	ORPHA:2297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2297	Insulin-resistance syndrome type A		HP:0001482	ORPHA:2297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2297	Insulin-resistance syndrome type A		HP:0002230	ORPHA:2297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2297	Insulin-resistance syndrome type A		HP:0005616	ORPHA:2297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2297	Insulin-resistance syndrome type A		HP:0005978	ORPHA:2297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2297	Insulin-resistance syndrome type A		HP:0007440	ORPHA:2297	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000028	ORPHA:228402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000194	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000232	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000248	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000252	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000272	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000280	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000337	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000664	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000733	ORPHA:228402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000749	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000750	ORPHA:228402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0000752	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0001250	ORPHA:228402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0001251	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0001252	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0001385	ORPHA:228402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0001510	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0001572	ORPHA:228402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0001852	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0002019	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0002230	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0002360	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0002553	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0002591	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0004209	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0004279	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0004322	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0008736	ORPHA:228402	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0010804	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0010864	ORPHA:228402	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228402	2q23.1 microdeletion syndrome		HP:0100716	ORPHA:228402	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69061	Idiopathic steroid-sensitive nephrotic syndrome		HP:0000100	ORPHA:69061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69061	Idiopathic steroid-sensitive nephrotic syndrome		HP:0001004	ORPHA:69061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000218	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000268	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000276	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000322	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000337	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000347	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000369	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000377	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000448	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000508	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000678	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0000951	ORPHA:228410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0001249	ORPHA:228410	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0001634	ORPHA:228410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0001642	ORPHA:228410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0001650	ORPHA:228410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0001654	ORPHA:228410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0001699	ORPHA:228410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0002750	ORPHA:228410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0004322	ORPHA:228410	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0005180	ORPHA:228410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0001382	ORPHA:228410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228410	Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome		HP:0011675	ORPHA:228410	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69063	Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization		HP:0000099	ORPHA:69063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69063	Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization		HP:0000100	ORPHA:69063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69063	Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization		HP:0030949	ORPHA:69063	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69063	Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization		HP:0031437	ORPHA:69063	TAS		HP:0040281			H	ORPHA:orphadata[2025-10-22]
ORPHA:69063	Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization		HP:0000083	ORPHA:69063	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0001075	ORPHA:48104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0001370	ORPHA:48104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0001945	ORPHA:48104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0002037	ORPHA:48104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0002829	ORPHA:48104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0002863	ORPHA:48104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0003326	ORPHA:48104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0008066	ORPHA:48104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0010702	ORPHA:48104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0012324	ORPHA:48104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0100614	ORPHA:48104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0200034	ORPHA:48104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0200037	ORPHA:48104	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0200039	ORPHA:48104	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:48104	Pyoderma gangrenosum		HP:0200042	ORPHA:48104	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000252	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000316	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000324	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000347	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000365	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000431	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000463	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0001290	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0001511	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0001643	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0002092	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0002205	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0002553	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0003196	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0004322	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0006801	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0008551	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0010864	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0011968	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0012418	ORPHA:2282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000028	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000037	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000047	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000049	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000054	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000185	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000470	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000508	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0000924	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2282	Dysmorphism-short stature-deafness-difference of sex development syndrome		HP:0011819	ORPHA:2282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0000600	ORPHA:2289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0000602	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0000639	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0000648	ORPHA:2289	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0000708	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0000726	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0001250	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0001251	ORPHA:2289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0001260	ORPHA:2289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0001276	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0001347	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0002167	ORPHA:2289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0002353	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0002650	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0003298	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0003312	ORPHA:2289	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0003457	ORPHA:2289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2289	Neuronal intranuclear inclusion disease		HP:0100022	ORPHA:2289	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2287	Fused mandibular incisors		HP:0000164	ORPHA:2287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2287	Fused mandibular incisors		HP:0006288	ORPHA:2287	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0000470	ORPHA:2285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0000496	ORPHA:2285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0000600	ORPHA:2285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0001608	ORPHA:2285	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0002691	ORPHA:2285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0003319	ORPHA:2285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0003468	ORPHA:2285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2285	Primary basilar invagination		HP:0005758	ORPHA:2285	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0000252	ORPHA:228415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0000545	ORPHA:228415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0000708	ORPHA:228415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0001249	ORPHA:228415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0001250	ORPHA:228415	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0001328	ORPHA:228415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0001510	ORPHA:228415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0002750	ORPHA:228415	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:228415	5q35 microduplication syndrome		HP:0004322	ORPHA:228415	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0000252	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0001249	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0001250	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0001263	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0001272	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0001290	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0001508	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0011968	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0012345	ORPHA:370921	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0000028	ORPHA:370921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0000046	ORPHA:370921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0000054	ORPHA:370921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370921	STT3A-CDG		HP:0007772	ORPHA:370921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000613	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001249	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001250	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001328	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001595	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001596	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0008064	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0008070	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0200034	ORPHA:2273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000499	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000614	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000726	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000962	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000964	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000966	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001268	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001508	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001510	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001597	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001804	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001812	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002046	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002205	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002223	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002376	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002718	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002719	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002721	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0004370	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0010783	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0011968	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0012742	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0045074	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0200020	ORPHA:2273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000023	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000028	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000072	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000077	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000126	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000252	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000400	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000453	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000483	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000491	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000492	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000498	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000509	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000545	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000554	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000639	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000682	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000925	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0000926	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001025	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001155	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001252	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001274	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001321	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001331	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0001539	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002007	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002120	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002251	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002750	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0002808	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0003468	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0003510	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0007957	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0010935	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0012157	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0012165	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0040163	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0100257	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0100308	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0100490	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0100532	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0100534	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome		HP:0100825	ORPHA:2273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0000252	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0000271	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0000958	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0001347	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0002445	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0003011	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0007021	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2271	Congenital ichthyosis-microcephalus-tetraplegia syndrome		HP:0008064	ORPHA:2271	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0000365	ORPHA:369939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0001508	ORPHA:369939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0001999	ORPHA:369939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0007256	ORPHA:369939	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0000252	ORPHA:369939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0000486	ORPHA:369939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0001511	ORPHA:369939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0001954	ORPHA:369939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0002445	ORPHA:369939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0006808	ORPHA:369939	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0000496	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0000648	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0000718	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0000752	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0001272	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0002120	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0003429	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0007371	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0012444	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369939	Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome		HP:0012762	ORPHA:369939	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0000218	ORPHA:171881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0000276	ORPHA:171881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0001270	ORPHA:171881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0001315	ORPHA:171881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0004303	ORPHA:171881	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0000767	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0001290	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0001611	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0001634	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0001763	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0002359	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0002421	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0002616	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0002938	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0002943	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0003388	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0003391	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0003551	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0003557	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0003700	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0006673	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0007110	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0007210	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0007340	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0008081	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0009046	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0010628	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0011703	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0030051	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:171881	Cap myopathy		HP:0030200	ORPHA:171881	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0002888	ORPHA:251639	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0002076	ORPHA:251639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0012531	ORPHA:251639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0025461	ORPHA:251639	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0001250	ORPHA:251639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0001288	ORPHA:251639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0002013	ORPHA:251639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0002460	ORPHA:251639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0010302	ORPHA:251639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0012534	ORPHA:251639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0030693	ORPHA:251639	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0002896	ORPHA:251639	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0100013	ORPHA:251639	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0100526	ORPHA:251639	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251639	Subependymoma		HP:0100615	ORPHA:251639	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0001249	ORPHA:2278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0001508	ORPHA:2278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0003510	ORPHA:2278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0007479	ORPHA:2278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0000164	ORPHA:2278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0000518	ORPHA:2278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0001231	ORPHA:2278	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0003355	ORPHA:2278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2278	Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome		HP:0008209	ORPHA:2278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0100006	ORPHA:251643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0005107	ORPHA:251643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0008069	ORPHA:251643	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0000372	ORPHA:251643	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0002888	ORPHA:251643	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0031938	ORPHA:251643	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0002013	ORPHA:251643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0002315	ORPHA:251643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0002317	ORPHA:251643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0005341	ORPHA:251643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0012700	ORPHA:251643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251643	Myxopapillary ependymoma		HP:0030833	ORPHA:251643	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0000726	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0001251	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0001265	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0001288	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0001744	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0002167	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0002240	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2274	Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome		HP:0008064	ORPHA:2274	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0001785	ORPHA:568051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0003550	ORPHA:568051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0003759	ORPHA:568051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0010741	ORPHA:568051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0100766	ORPHA:568051	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0000282	ORPHA:568051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0001581	ORPHA:568051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0002619	ORPHA:568051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0005293	ORPHA:568051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0007514	ORPHA:568051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0100658	ORPHA:568051	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0000508	ORPHA:568051	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:568051	GJC2-related late-onset primary lymphedema		HP:0031188	ORPHA:568051	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0000246	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0000388	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0000988	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001287	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001369	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001508	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001864	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001873	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001874	ORPHA:229717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001903	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001945	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0001999	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0002014	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0002024	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0002090	ORPHA:229717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0002205	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0002721	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0002960	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0004322	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0004332	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0012378	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0100533	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0100658	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0100763	ORPHA:229717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0100765	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0100806	ORPHA:229717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0100838	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:229717	Non-syndromic agammaglobulinemia		HP:0200042	ORPHA:229717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000047	ORPHA:2261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000174	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000243	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000252	ORPHA:2261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000358	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000396	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000444	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0000664	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0001231	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0001249	ORPHA:2261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0001252	ORPHA:2261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0001387	ORPHA:2261	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0004209	ORPHA:2261	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0008388	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2261	Hypospadias-intellectual disability, Goldblatt type syndrome		HP:0011800	ORPHA:2261	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000083	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000093	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0003259	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0005563	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0012213	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0012575	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0012584	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0030162	ORPHA:2260	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000092	ORPHA:2260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0001518	ORPHA:2260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0001622	ORPHA:2260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0003774	ORPHA:2260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0011035	ORPHA:2260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0025361	ORPHA:2260	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0001944	ORPHA:2260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0001959	ORPHA:2260	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000122	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000271	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000347	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000365	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000588	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000776	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0000822	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0001250	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0001684	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0002089	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0006518	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0009796	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0012758	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2260	Oligomeganephronia		HP:0040064	ORPHA:2260	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0000822	ORPHA:369929	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0000859	ORPHA:369929	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0040084	ORPHA:369929	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0001250	ORPHA:369929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0001263	ORPHA:369929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0001714	ORPHA:369929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002900	ORPHA:369929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0100021	ORPHA:369929	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0001258	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0001959	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002069	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002092	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002305	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002384	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0010864	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0011166	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0011410	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0011706	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0100285	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0100704	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0200114	ORPHA:369929	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0000360	ORPHA:369929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0000421	ORPHA:369929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0000787	ORPHA:369929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0001629	ORPHA:369929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002018	ORPHA:369929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002170	ORPHA:369929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0002315	ORPHA:369929	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome		HP:0008221	ORPHA:369929	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:369929	Primary hyperaldosteronism-seizures-neurological abnormalities syndrome	NOT	HP:0011739	ORPHA:369929	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0001249	ORPHA:2269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0002221	ORPHA:2269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0002293	ORPHA:2269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0002555	ORPHA:2269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0005597	ORPHA:2269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0007503	ORPHA:2269	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0000656	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0000958	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0000973	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0001263	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0002194	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0002317	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0005595	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0012472	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0025092	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0031936	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0040189	ORPHA:2269	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0001344	ORPHA:2269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome		HP:0045075	ORPHA:2269	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	NOT	HP:0000135	ORPHA:2269	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	NOT	HP:0001103	ORPHA:2269	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	NOT	HP:0001250	ORPHA:2269	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	NOT	HP:0001257	ORPHA:2269	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	NOT	HP:0002063	ORPHA:2269	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	NOT	HP:0010550	ORPHA:2269	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2269	Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome	NOT	HP:0030182	ORPHA:2269	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0002888	ORPHA:251636	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0002076	ORPHA:251636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0012531	ORPHA:251636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0025461	ORPHA:251636	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0001250	ORPHA:251636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0001288	ORPHA:251636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0002013	ORPHA:251636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0002460	ORPHA:251636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0010302	ORPHA:251636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0012534	ORPHA:251636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0030693	ORPHA:251636	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0002896	ORPHA:251636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0100013	ORPHA:251636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0100526	ORPHA:251636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251636	Ependymoma		HP:0100615	ORPHA:251636	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0000158	ORPHA:2268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0000256	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0000286	ORPHA:2268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0000316	ORPHA:2268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0000347	ORPHA:2268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0000369	ORPHA:2268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0001249	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0001263	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0001334	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0001537	ORPHA:2268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0001874	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0001888	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0001903	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0002024	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0002205	ORPHA:2268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0002721	ORPHA:2268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0003220	ORPHA:2268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0004313	ORPHA:2268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0004322	ORPHA:2268	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0005280	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0005374	ORPHA:2268	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0010808	ORPHA:2268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2268	ICF syndrome		HP:0012368	ORPHA:2268	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2266	Hypotrichosis-intellectual disability, Lopes type		HP:0001249	ORPHA:2266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2266	Hypotrichosis-intellectual disability, Lopes type		HP:0006088	ORPHA:2266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2266	Hypotrichosis-intellectual disability, Lopes type		HP:0006288	ORPHA:2266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2266	Hypotrichosis-intellectual disability, Lopes type		HP:0008070	ORPHA:2266	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0000238	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0000716	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0001181	ORPHA:275543	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0001249	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0001250	ORPHA:275543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0001257	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0001263	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0001288	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0001347	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0002017	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0002251	ORPHA:275543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0002315	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0002410	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0002463	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0003202	ORPHA:275543	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275543	L1 syndrome		HP:0004374	ORPHA:275543	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0001635	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0001639	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0001658	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0002202	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0003115	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0006530	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0010741	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0031327	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0100598	ORPHA:330001	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0000763	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0002028	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0002240	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0002254	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0002495	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0002579	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0002607	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0003155	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0004926	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0005110	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0005341	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0011675	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0012185	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0012332	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0200101	ORPHA:330001	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0000083	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0000093	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0000100	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0000112	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0001650	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0001662	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0001824	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:330001	Wild type ATTR amyloidosis		HP:0003416	ORPHA:330001	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0002960	ORPHA:227990	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001972	ORPHA:227990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0002582	ORPHA:227990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0002608	ORPHA:227990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0030057	ORPHA:227990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0100651	ORPHA:227990	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001045	ORPHA:227990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001596	ORPHA:227990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001882	ORPHA:227990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0002613	ORPHA:227990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0004313	ORPHA:227990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0010625	ORPHA:227990	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0000217	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0000815	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0000863	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0000938	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001094	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001097	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001370	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001970	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0001973	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0003613	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0006530	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0008066	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0010451	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0012115	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0012220	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4		HP:0100522	ORPHA:227990	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4	NOT	HP:0000872	ORPHA:227990	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4	NOT	HP:0002728	ORPHA:227990	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4	NOT	HP:0008207	ORPHA:227990	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:227990	Autoimmune polyendocrinopathy type 4	NOT	HP:0100647	ORPHA:227990	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0000953	ORPHA:2251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0001596	ORPHA:2251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0003510	ORPHA:2251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0008070	ORPHA:2251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0009778	ORPHA:2251	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0000232	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0000411	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0000982	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0001025	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0001053	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0001199	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0001249	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0001263	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0001328	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0002300	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0002381	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0002381	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0006482	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0008402	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0010529	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0040036	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0100490	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0100798	ORPHA:2251	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2251	Thumb deformity-alopecia-pigmentation anomaly syndrome		HP:0006101	ORPHA:2251	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158008	Papular xanthoma		HP:0001013	ORPHA:158008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158008	Papular xanthoma		HP:0100727	ORPHA:158008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158008	Papular xanthoma		HP:0200035	ORPHA:158008	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158008	Papular xanthoma	NOT	HP:0003077	ORPHA:158008	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000518	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000692	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0003241	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0004409	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0006352	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0008736	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0009927	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0009932	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0040326	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0100596	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000028	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000044	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000327	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000453	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000528	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000568	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000572	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000612	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000618	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000646	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000771	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0009023	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0009924	ORPHA:2250	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000175	ORPHA:2250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000176	ORPHA:2250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000193	ORPHA:2250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000648	ORPHA:2250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0030752	ORPHA:2250	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000023	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000135	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000309	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2250	Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome		HP:0000458	ORPHA:2250	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158003	Xanthoma disseminatum		HP:0002797	ORPHA:158003	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158003	Xanthoma disseminatum		HP:0000873	ORPHA:158003	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158003	Xanthoma disseminatum		HP:0000159	ORPHA:158003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158003	Xanthoma disseminatum		HP:0000600	ORPHA:158003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158003	Xanthoma disseminatum		HP:0001600	ORPHA:158003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158003	Xanthoma disseminatum		HP:0025426	ORPHA:158003	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000303	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000343	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000400	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000712	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000718	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000742	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0001263	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0002378	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0002465	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0002515	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0002705	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0010864	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0045025	ORPHA:457212	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000073	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000574	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000748	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0000821	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0002540	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0002861	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0003002	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0005580	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:457212	Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome		HP:0012114	ORPHA:457212	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0000490	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0000540	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0000639	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0001249	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0001357	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0001513	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0002079	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0002119	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0002194	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0007020	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0011220	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0011400	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0025312	ORPHA:521390	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:521390	Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome		HP:0001561	ORPHA:521390	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0000498	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0000501	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0000520	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0000554	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0000572	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0001101	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0002086	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0005547	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0007565	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0011830	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0011886	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158000	Juvenile xanthogranuloma		HP:0200064	ORPHA:158000	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002089	ORPHA:2257	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0000961	ORPHA:2257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002091	ORPHA:2257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002104	ORPHA:2257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002643	ORPHA:2257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002789	ORPHA:2257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0012418	ORPHA:2257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0030829	ORPHA:2257	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0000175	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0000252	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0000286	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0000347	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0000369	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0001508	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0001511	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0001651	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0001684	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002205	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002778	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0003065	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0040045	ORPHA:2257	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0000071	ORPHA:2257	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002099	ORPHA:2257	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0002107	ORPHA:2257	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia		HP:0030966	ORPHA:2257	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2257	Primary pulmonary hypoplasia	NOT	HP:0032094	ORPHA:2257	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000316	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000347	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000411	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000431	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000494	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0001561	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0001622	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0002007	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0003022	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0003026	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0005280	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0006101	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0006492	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0010242	ORPHA:2256	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000028	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000049	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0000089	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0001195	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0001629	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0008736	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0030680	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2256	Fibulo-ulnar hypoplasia-renal anomalies syndrome		HP:0100016	ORPHA:2256	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0011752	ORPHA:251623	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0011754	ORPHA:251623	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0012503	ORPHA:251623	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0001123	ORPHA:251623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0002315	ORPHA:251623	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0000044	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0000141	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0000802	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0000824	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0000870	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0002354	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0008214	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0008245	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0011043	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0012378	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0030018	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0040075	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0040171	ORPHA:251623	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0000863	ORPHA:251623	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:251623	Pituicytoma		HP:0100829	ORPHA:251623	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0000857	ORPHA:2255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001629	ORPHA:2255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001631	ORPHA:2255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001655	ORPHA:2255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001738	ORPHA:2255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001249	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001508	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001511	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001518	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0002254	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0002594	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0011968	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0100790	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0100801	ORPHA:2255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0000851	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001250	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001319	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001562	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001636	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001642	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001643	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001669	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0002098	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0003645	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0004415	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0004762	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0011573	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0011581	ORPHA:2255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0000073	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0000776	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0000891	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001195	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0001537	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0002566	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0005912	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0010626	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0011466	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0011611	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0011628	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2255	Pancreatic hypoplasia-diabetes-congenital heart disease syndrome		HP:0040196	ORPHA:2255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0003765	ORPHA:279914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0031035	ORPHA:279914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0200056	ORPHA:279914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0040049	ORPHA:279914	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0000501	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0000518	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0000585	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0002633	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0007663	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0011484	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0011505	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0012122	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0030652	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0030661	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0100014	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0100653	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0100832	ORPHA:279914	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279914	Intermediate uveitis		HP:0001970	ORPHA:279914	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0001919	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0002360	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0002960	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0003259	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0005202	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0012622	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0100651	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0000093	ORPHA:275555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0000822	ORPHA:275555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0004421	ORPHA:275555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0005117	ORPHA:275555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0100767	ORPHA:275555	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0000083	ORPHA:275555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0100598	ORPHA:275555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0410019	ORPHA:275555	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0000077	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0000504	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0000707	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0001511	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0001518	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0002027	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0002315	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0002910	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0006707	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0031418	ORPHA:275555	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0000147	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:275555	Preeclampsia		HP:0001873	ORPHA:275555	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001252	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001263	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001265	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001270	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001324	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0002398	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0002878	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0003202	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0007360	ORPHA:2254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0000253	ORPHA:2254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0000529	ORPHA:2254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0000639	ORPHA:2254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0000648	ORPHA:2254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001508	ORPHA:2254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0011968	ORPHA:2254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0012110	ORPHA:2254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0000486	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001250	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001257	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001308	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001347	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0002120	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0002350	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0003477	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0004886	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0033725	ORPHA:2254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0000565	ORPHA:2254	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0001251	ORPHA:2254	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2254	Pontocerebellar hypoplasia type 1		HP:0002804	ORPHA:2254	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2253	Foveal hypoplasia-presenile cataract syndrome		HP:0000478	ORPHA:2253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2253	Foveal hypoplasia-presenile cataract syndrome		HP:0000486	ORPHA:2253	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2253	Foveal hypoplasia-presenile cataract syndrome		HP:0000518	ORPHA:2253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2253	Foveal hypoplasia-presenile cataract syndrome		HP:0000639	ORPHA:2253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2253	Foveal hypoplasia-presenile cataract syndrome		HP:0000648	ORPHA:2253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2253	Foveal hypoplasia-presenile cataract syndrome		HP:0000504	ORPHA:2253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2253	Foveal hypoplasia-presenile cataract syndrome		HP:0007440	ORPHA:2253	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2252	Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome		HP:0000047	ORPHA:2252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2252	Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome		HP:0000303	ORPHA:2252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2252	Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome		HP:0002983	ORPHA:2252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2252	Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome		HP:0002984	ORPHA:2252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2252	Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome		HP:0005725	ORPHA:2252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2252	Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome		HP:0007477	ORPHA:2252	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0000286	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0000597	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0000602	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0001249	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0001276	ORPHA:99735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0001288	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0001324	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0001376	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0001608	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0002015	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0002094	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0002099	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0002486	ORPHA:99735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0003307	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0003326	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0003394	ORPHA:99735	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0003457	ORPHA:99735	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0003712	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0003720	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0004322	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99735	Myotonia permanens		HP:0100749	ORPHA:99735	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0000597	ORPHA:99736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0000602	ORPHA:99736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0000821	ORPHA:99736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0001276	ORPHA:99736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0001288	ORPHA:99736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0002015	ORPHA:99736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0002486	ORPHA:99736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0003326	ORPHA:99736	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0003394	ORPHA:99736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0003457	ORPHA:99736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0003712	ORPHA:99736	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99736	Acetazolamide-responsive myotonia		HP:0100749	ORPHA:99736	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000044	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000511	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000545	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000617	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000639	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000668	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000677	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000684	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000823	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001251	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001256	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001257	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001263	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001310	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001321	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001332	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0001347	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002015	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002079	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002080	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002134	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002174	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002312	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002376	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002403	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002415	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002464	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002493	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0003429	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0003487	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0004322	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0005341	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0025460	ORPHA:447896	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000648	ORPHA:447896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002120	ORPHA:447896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002166	ORPHA:447896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0002307	ORPHA:447896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0006858	ORPHA:447896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0009830	ORPHA:447896	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0000490	ORPHA:447896	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome		HP:0007359	ORPHA:447896	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0003552	ORPHA:99734	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0100284	ORPHA:99734	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0002491	ORPHA:99734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0008967	ORPHA:99734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0012902	ORPHA:99734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0012903	ORPHA:99734	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0000622	ORPHA:99734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0000651	ORPHA:99734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0003326	ORPHA:99734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0012378	ORPHA:99734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0012899	ORPHA:99734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0012900	ORPHA:99734	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0000486	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0001288	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0001319	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0002104	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0003701	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0003740	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0010307	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0025425	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans		HP:0030842	ORPHA:99734	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:99734	Myotonia fluctuans	NOT	HP:0012904	ORPHA:99734	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0001643	ORPHA:2248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0001718	ORPHA:2248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0009800	ORPHA:2248	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0012304	ORPHA:2248	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0001631	ORPHA:2248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0002916	ORPHA:2248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0004383	ORPHA:2248	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2248	Hypoplastic left heart syndrome		HP:0011560	ORPHA:2248	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0000505	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0000512	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0000639	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0000648	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0001251	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0001252	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0001321	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0007703	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2246	Cerebellar hypoplasia-tapetoretinal degeneration syndrome		HP:0100543	ORPHA:2246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0000952	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001396	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002155	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002904	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003073	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003119	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003128	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003155	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0004313	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0006254	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0008151	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0011966	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0012024	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0025435	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0030948	ORPHA:247598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001397	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001433	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001531	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001987	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002014	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002161	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002240	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002910	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003231	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0010903	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0010909	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0010916	ORPHA:247598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001511	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001903	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002239	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0002919	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003124	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003141	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003233	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003235	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0003354	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0004396	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0012278	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0040301	ORPHA:247598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0000518	ORPHA:247598	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247598	Neonatal intrahepatic cholestasis due to citrin deficiency		HP:0001892	ORPHA:247598	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0000021	ORPHA:2241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0002017	ORPHA:2241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0003270	ORPHA:2241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0004388	ORPHA:2241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0100771	ORPHA:2241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0000003	ORPHA:2241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0000072	ORPHA:2241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0001561	ORPHA:2241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0002566	ORPHA:2241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0011024	ORPHA:2241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0000028	ORPHA:2241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0001522	ORPHA:2241	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0001537	ORPHA:2241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0001539	ORPHA:2241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0030680	ORPHA:2241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0100544	ORPHA:2241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2241	Megacystis-microcolon-intestinal hypoperistalsis syndrome		HP:0100806	ORPHA:2241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0000098	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0000141	ORPHA:99725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0000280	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0000303	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0000870	ORPHA:99725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0000845	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0000975	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0001176	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0001639	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0001712	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0001833	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0002007	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0005616	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0005978	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0006767	ORPHA:99725	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0011407	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0011760	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0012411	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0030269	ORPHA:99725	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:99725	Pituitary gigantism		HP:0100829	ORPHA:99725	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0000239	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0000270	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001249	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001252	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001263	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001328	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001387	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001802	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001817	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001840	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0001883	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0002983	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0002984	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0003022	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0003027	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0003042	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0003510	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0009465	ORPHA:2249	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0010059	ORPHA:2249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2249	Ulna hypoplasia-intellectual disability syndrome		HP:0011304	ORPHA:2249	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0002315	ORPHA:238624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0002516	ORPHA:238624	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0001085	ORPHA:238624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0001513	ORPHA:238624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0012393	ORPHA:238624	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0000572	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0000613	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0000622	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0000651	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0002013	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0002018	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0002360	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0010822	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0100851	ORPHA:238624	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0000716	ORPHA:238624	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0001254	ORPHA:238624	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0002076	ORPHA:238624	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0002321	ORPHA:238624	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0003418	ORPHA:238624	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0008629	ORPHA:238624	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238624	Idiopathic intracranial hypertension		HP:0011161	ORPHA:238624	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria		HP:0000112	ORPHA:69076	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria		HP:0000124	ORPHA:69076	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria		HP:0003076	ORPHA:69076	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria		HP:0000010	ORPHA:69076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria		HP:0001944	ORPHA:69076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria		HP:0001946	ORPHA:69076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria		HP:0008855	ORPHA:69076	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria	NOT	HP:0000805	ORPHA:69076	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria	NOT	HP:0000855	ORPHA:69076	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria	NOT	HP:0003074	ORPHA:69076	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria	NOT	HP:0004924	ORPHA:69076	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria	NOT	HP:0040214	ORPHA:69076	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69076	Familial renal glucosuria	NOT	HP:0040217	ORPHA:69076	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0000737	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0000790	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0000822	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0001482	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0001824	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0001873	ORPHA:69077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0001903	ORPHA:69077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0001945	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0002017	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0002027	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0002093	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0002301	ORPHA:69077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0002315	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0002716	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0002896	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0003072	ORPHA:69077	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0004396	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0006824	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0009726	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0011029	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0012246	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0100006	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0100021	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69077	Rhabdoid tumor		HP:0100242	ORPHA:69077	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0000077	ORPHA:69078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0001482	ORPHA:69078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0001824	ORPHA:69078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0002017	ORPHA:69078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0002027	ORPHA:69078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0002619	ORPHA:69078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0003401	ORPHA:69078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0012378	ORPHA:69078	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69078	Liposarcoma		HP:0100242	ORPHA:69078	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158025	Hereditary progressive mucinous histiocytosis		HP:0025475	ORPHA:158025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158025	Hereditary progressive mucinous histiocytosis		HP:0030350	ORPHA:158025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158025	Hereditary progressive mucinous histiocytosis		HP:0040138	ORPHA:158025	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158025	Hereditary progressive mucinous histiocytosis		HP:0000989	ORPHA:158025	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158025	Hereditary progressive mucinous histiocytosis	NOT	HP:0002716	ORPHA:158025	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:158025	Hereditary progressive mucinous histiocytosis	NOT	HP:0031871	ORPHA:158025	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:370091	Oculocutaneous albinism type 5		HP:0000218	ORPHA:370091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370091	Oculocutaneous albinism type 5		HP:0000613	ORPHA:370091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370091	Oculocutaneous albinism type 5		HP:0000639	ORPHA:370091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370091	Oculocutaneous albinism type 5		HP:0001098	ORPHA:370091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370091	Oculocutaneous albinism type 5		HP:0001107	ORPHA:370091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370091	Oculocutaneous albinism type 5		HP:0007663	ORPHA:370091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:370091	Oculocutaneous albinism type 5		HP:0007750	ORPHA:370091	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000110	ORPHA:2237	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000408	ORPHA:2237	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000829	ORPHA:2237	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000076	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000083	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000113	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000122	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000126	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000860	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0002199	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0002901	ORPHA:2237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000819	ORPHA:2237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0001153	ORPHA:2237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0003762	ORPHA:2237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000148	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000151	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000175	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0000510	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0001627	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0003765	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0008850	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2237	Hypoparathyroidism-sensorineural deafness-renal disease syndrome		HP:0011840	ORPHA:2237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158022	Progressive nodular histiocytosis		HP:0001482	ORPHA:158022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158022	Progressive nodular histiocytosis		HP:0001945	ORPHA:158022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158022	Progressive nodular histiocytosis		HP:0004326	ORPHA:158022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158022	Progressive nodular histiocytosis		HP:0200034	ORPHA:158022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000044	ORPHA:2235	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000510	ORPHA:2235	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000580	ORPHA:2235	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000144	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000786	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000823	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000830	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000939	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0002750	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0003164	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0003187	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0008187	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0008202	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0008240	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0008724	ORPHA:2235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0000164	ORPHA:2235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0001513	ORPHA:2235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0002757	ORPHA:2235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0004322	ORPHA:2235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2235	Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome		HP:0004349	ORPHA:2235	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000046	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000135	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000144	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000708	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000771	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0001249	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0002937	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0003312	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0003782	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0005978	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0008734	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0008736	ORPHA:2234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000470	ORPHA:2234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000772	ORPHA:2234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0000820	ORPHA:2234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0001513	ORPHA:2234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0002231	ORPHA:2234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0004322	ORPHA:2234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2234	Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome		HP:0100745	ORPHA:2234	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0000035	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0000135	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0000144	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0000218	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0000470	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0000771	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0001256	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0001513	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0002162	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0004322	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0005916	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0011362	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0040071	ORPHA:2233	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0000494	ORPHA:2233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2233	Hypogonadism-mitral valve prolapse-intellectual disability syndrome		HP:0001634	ORPHA:2233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001397	ORPHA:247585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0008281	ORPHA:247585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0011966	ORPHA:247585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0045082	ORPHA:247585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000711	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000718	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000737	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000738	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000746	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001250	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001254	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001289	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001337	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002155	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002240	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002329	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002354	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002360	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002910	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0003073	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0003075	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0003077	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0007159	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0012164	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0030166	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0030765	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0031258	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0100738	ORPHA:247585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000709	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000752	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0000805	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001259	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001263	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001395	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001402	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0001733	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002013	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002014	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002181	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0002480	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0003124	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0003233	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0010529	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0012569	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0100754	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247585	Citrullinemia type II		HP:0100785	ORPHA:247585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000815	ORPHA:2232	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0002293	ORPHA:2232	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0008193	ORPHA:2232	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000028	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000219	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000534	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000786	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000789	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000802	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000823	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000837	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000938	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000939	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0001510	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0001596	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0003187	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0003799	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0005469	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0007464	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0008187	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0008214	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0008633	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0008684	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0010463	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0010464	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0011961	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0040171	ORPHA:2232	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000252	ORPHA:2232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0001256	ORPHA:2232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0002225	ORPHA:2232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0002652	ORPHA:2232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0002808	ORPHA:2232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0002938	ORPHA:2232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0045075	ORPHA:2232	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0000365	ORPHA:2232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0001199	ORPHA:2232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0003393	ORPHA:2232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0006184	ORPHA:2232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0009185	ORPHA:2232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0010487	ORPHA:2232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2232	Primary hypergonadotropic hypogonadism-partial alopecia syndrome		HP:0012506	ORPHA:2232	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370097	Oculocutaneous albinism type 6		HP:0000613	ORPHA:370097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370097	Oculocutaneous albinism type 6		HP:0000639	ORPHA:370097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370097	Oculocutaneous albinism type 6		HP:0001098	ORPHA:370097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370097	Oculocutaneous albinism type 6		HP:0007663	ORPHA:370097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370097	Oculocutaneous albinism type 6		HP:0008034	ORPHA:370097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370097	Oculocutaneous albinism type 6		HP:0008059	ORPHA:370097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370097	Oculocutaneous albinism type 6		HP:0030613	ORPHA:370097	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0002960	ORPHA:525731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0011703	ORPHA:525731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0011784	ORPHA:525731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0031506	ORPHA:525731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0100647	ORPHA:525731	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000237	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000492	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000520	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000712	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000737	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000752	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000853	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000975	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001337	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001508	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001744	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001959	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001962	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0002014	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0002240	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0002487	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0002591	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0002910	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0005616	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0008373	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0011788	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0025379	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0031284	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0100785	ORPHA:525731	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000708	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000822	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000952	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001363	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001511	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001562	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001622	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001873	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0002017	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0005110	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0010519	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0100534	ORPHA:525731	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000252	ORPHA:525731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0000491	ORPHA:525731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001263	ORPHA:525731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001635	ORPHA:525731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0001904	ORPHA:525731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0012768	ORPHA:525731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:525731	Pediatric-onset Graves disease		HP:0200028	ORPHA:525731	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000154	ORPHA:319671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000445	ORPHA:319671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000490	ORPHA:319671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000687	ORPHA:319671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0008897	ORPHA:319671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0010864	ORPHA:319671	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000272	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000322	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000325	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000369	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000733	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000739	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000965	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0001072	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0012471	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0012745	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0040196	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0045025	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0045075	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0100738	ORPHA:319671	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000315	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000486	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0000742	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0001250	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0001631	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0002360	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0002650	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0003100	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0010535	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0011220	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319671	Alazami syndrome		HP:0012171	ORPHA:319671	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447877	Polymerase proofreading-related polyposis		HP:0005227	ORPHA:447877	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447877	Polymerase proofreading-related polyposis		HP:0012114	ORPHA:447877	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447877	Polymerase proofreading-related polyposis		HP:0200063	ORPHA:447877	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:447877	Polymerase proofreading-related polyposis		HP:0003002	ORPHA:447877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447877	Polymerase proofreading-related polyposis		HP:0030692	ORPHA:447877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447877	Polymerase proofreading-related polyposis		HP:0040276	ORPHA:447877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:447877	Polymerase proofreading-related polyposis		HP:0100743	ORPHA:447877	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0000252	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0000448	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0000601	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0000786	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0001191	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0001250	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0001263	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0001385	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0001513	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0001607	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0002750	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0003067	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0004209	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0004220	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0004322	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0004626	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0008551	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0008846	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0008850	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0009826	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0010864	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:319675	Microcephalic primordial dwarfism, Dauber type		HP:0012814	ORPHA:319675	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0002901	ORPHA:2239	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0008198	ORPHA:2239	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0008211	ORPHA:2239	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0002150	ORPHA:2239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0002199	ORPHA:2239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0002905	ORPHA:2239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0003251	ORPHA:2239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2239	Familial isolated hypoparathyroidism due to agenesis of parathyroid gland		HP:0002917	ORPHA:2239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0007352	ORPHA:2238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0000829	ORPHA:2238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0001250	ORPHA:2238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0002901	ORPHA:2238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0003198	ORPHA:2238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0100530	ORPHA:2238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0000518	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0000682	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0000684	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0001324	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0002514	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0002905	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0003394	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0003472	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0011675	ORPHA:2238	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0000112	ORPHA:2238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0004322	ORPHA:2238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0025425	ORPHA:2238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2238	Familial isolated hypoparathyroidism		HP:0031627	ORPHA:2238	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0007427	ORPHA:69087	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0007455	ORPHA:69087	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000164	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000958	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000966	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0001808	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0002046	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0006482	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0007500	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0008392	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0008404	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0031282	ORPHA:69087	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000670	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000970	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0000972	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0001010	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0001056	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0001220	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0001806	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0001810	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0005586	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0006253	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0006286	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0006297	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0006480	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0007530	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0007599	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0011069	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0012785	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69087	Naegeli-Franceschetti-Jadassohn syndrome		HP:0031045	ORPHA:69087	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0002960	ORPHA:227982	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0000872	ORPHA:227982	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001972	ORPHA:227982	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0002582	ORPHA:227982	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0002608	ORPHA:227982	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0030057	ORPHA:227982	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0100647	ORPHA:227982	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0100651	ORPHA:227982	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001045	ORPHA:227982	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001596	ORPHA:227982	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001882	ORPHA:227982	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0002613	ORPHA:227982	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0004313	ORPHA:227982	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0010625	ORPHA:227982	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0000217	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0000815	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0000863	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0000938	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001094	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001097	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001370	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001970	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0001973	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0003613	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0006530	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0008066	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0010451	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0011771	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0012115	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0012220	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3		HP:0100522	ORPHA:227982	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3	NOT	HP:0002728	ORPHA:227982	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:227982	Autoimmune polyendocrinopathy type 3	NOT	HP:0008207	ORPHA:227982	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000564	ORPHA:69085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0001092	ORPHA:69085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0002557	ORPHA:69085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0002561	ORPHA:69085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0012814	ORPHA:69085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0100783	ORPHA:69085	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000175	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000193	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000498	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000668	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000958	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000966	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0001159	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0001770	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0002164	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0004209	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0007717	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0011819	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0011939	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0012165	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0410005	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0410030	ORPHA:69085	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000151	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000272	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000411	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0000786	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0001480	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0001596	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0003765	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0007565	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0010463	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:69085	Limb-mammary syndrome		HP:0045075	ORPHA:69085	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0000028	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0000501	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0000648	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0000737	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0000762	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0001263	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0001332	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0001344	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0002020	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0002059	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0002069	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0002353	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0002540	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0003202	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0003390	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0004302	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0007002	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0007817	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0008366	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0008872	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0008947	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0011344	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0011471	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0030179	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0100660	ORPHA:457205	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:457205	Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome		HP:0012411	ORPHA:457205	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0001250	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0001482	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0001903	ORPHA:158014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0001945	ORPHA:158014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0002315	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0002716	ORPHA:158014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0002797	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0002961	ORPHA:158014	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0003401	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0010550	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0010783	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158014	Rosaï-Dorfman disease		HP:0200034	ORPHA:158014	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2224	Hypertryptophanemia		HP:0003144	ORPHA:2224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2224	Hypertryptophanemia		HP:0003361	ORPHA:2224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2224	Hypertryptophanemia		HP:0500134	ORPHA:2224	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2222	Hypertrichosis lanuginosa congenita		HP:0000164	ORPHA:2222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2222	Hypertrichosis lanuginosa congenita		HP:0000212	ORPHA:2222	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2222	Hypertrichosis lanuginosa congenita		HP:0000365	ORPHA:2222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2222	Hypertrichosis lanuginosa congenita		HP:0000574	ORPHA:2222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2222	Hypertrichosis lanuginosa congenita		HP:0000684	ORPHA:2222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2222	Hypertrichosis lanuginosa congenita		HP:0001000	ORPHA:2222	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2222	Hypertrichosis lanuginosa congenita		HP:0002230	ORPHA:2222	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0011446	ORPHA:279947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0012378	ORPHA:279947	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000366	ORPHA:279947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000737	ORPHA:279947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000822	ORPHA:279947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000975	ORPHA:279947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0001945	ORPHA:279947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0002315	ORPHA:279947	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000217	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000613	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000622	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000716	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0000750	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0001260	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0001324	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0001609	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0001962	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:279947	Postorgasmic illness syndrome		HP:0003552	ORPHA:279947	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0000492	ORPHA:2221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0000534	ORPHA:2221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0002213	ORPHA:2221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0002230	ORPHA:2221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0002664	ORPHA:2221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0005599	ORPHA:2221	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0000158	ORPHA:2221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0000206	ORPHA:2221	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0000956	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0001072	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0001824	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0002028	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0002716	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0004396	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0008064	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0100013	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0100606	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2221	Acquired hypertrichosis lanuginosa		HP:0100615	ORPHA:2221	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0002230	ORPHA:2220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0002983	ORPHA:2220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0003510	ORPHA:2220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0008905	ORPHA:2220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0009811	ORPHA:2220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0011121	ORPHA:2220	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000311	ORPHA:2220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000324	ORPHA:2220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0002300	ORPHA:2220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0002381	ORPHA:2220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0010529	ORPHA:2220	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000252	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000271	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000348	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000426	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000464	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000492	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000494	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000499	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000508	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000574	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0000614	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0001249	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0001263	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0001328	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0002750	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2220	Hypertrichosis cubiti		HP:0001382	ORPHA:2220	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0000504	ORPHA:280921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0000622	ORPHA:280921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0007663	ORPHA:280921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0025337	ORPHA:280921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0030652	ORPHA:280921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0200026	ORPHA:280921	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0000518	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0000613	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0000616	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0002315	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0011484	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0011505	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0030661	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0030953	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0100832	ORPHA:280921	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0000618	ORPHA:280921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0007906	ORPHA:280921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0011506	ORPHA:280921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:280921	Idiopathic panuveitis		HP:0100014	ORPHA:280921	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2229	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome		HP:0000147	ORPHA:2229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2229	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome		HP:0000431	ORPHA:2229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2229	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome		HP:0000508	ORPHA:2229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2229	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome		HP:0000815	ORPHA:2229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2229	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome		HP:0000826	ORPHA:2229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2229	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome		HP:0001644	ORPHA:2229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2229	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome		HP:0100362	ORPHA:2229	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0000147	ORPHA:2228	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0000164	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0000232	ORPHA:2228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0000668	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0000684	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0000698	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0001231	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0001597	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0001800	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0001804	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0001808	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0002213	ORPHA:2228	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0006349	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0006482	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0008402	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2228	Hypodontia-dysplasia of nails syndrome		HP:0012746	ORPHA:2228	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0012156	ORPHA:158048	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001744	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001876	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001945	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0012647	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0025540	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0031406	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0031691	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0032169	ORPHA:158048	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0000707	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001873	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001875	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001903	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0002155	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0002240	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0002910	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0003281	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0005521	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0011900	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0032204	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0040089	ORPHA:158048	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001250	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001251	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001260	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0002152	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0006824	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0012229	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0020101	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0030891	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0031179	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0031692	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0032260	ORPHA:158048	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0001298	ORPHA:158048	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0031700	ORPHA:158048	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158048	Hemophagocytic syndrome associated with an infection		HP:0032256	ORPHA:158048	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:238606	Primary orthostatic tremor		HP:0001337	ORPHA:238606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238606	Primary orthostatic tremor		HP:0002071	ORPHA:238606	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:238606	Primary orthostatic tremor		HP:0003011	ORPHA:238606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238606	Primary orthostatic tremor		HP:0003326	ORPHA:238606	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:238606	Primary orthostatic tremor		HP:0003394	ORPHA:238606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238606	Primary orthostatic tremor		HP:0003457	ORPHA:238606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:238606	Primary orthostatic tremor		HP:0100022	ORPHA:238606	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000277	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000298	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000324	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000343	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000358	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000465	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001182	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001357	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001762	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001840	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0002650	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0002804	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0003202	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0005487	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0005988	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0009465	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0100490	ORPHA:2215	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000028	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000046	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000160	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000175	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000405	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000426	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000494	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000508	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000601	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000767	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001166	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001611	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0002047	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0002714	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0003510	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0006610	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0009775	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0011302	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0012370	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0012400	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0040081	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0045040	ORPHA:2215	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000023	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000187	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000268	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000293	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000340	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000520	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0000772	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001252	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001557	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001561	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001804	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0001812	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0002094	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0002263	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0002808	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0005306	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0006101	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0006288	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0008402	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0010733	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0011800	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0040036	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0100556	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2215	Multiple pterygium-malignant hyperthermia syndrome		HP:0100798	ORPHA:2215	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0000252	ORPHA:2213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0000316	ORPHA:2213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0000413	ORPHA:2213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0009099	ORPHA:2213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0008551	ORPHA:2213	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0000085	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0000405	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0001249	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0001263	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0001328	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0003393	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0003510	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0004736	ORPHA:2213	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0000456	ORPHA:2213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2213	Hypertelorism-microtia-facial clefting syndrome		HP:0011803	ORPHA:2213	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000036	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000039	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000047	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000049	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000239	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000248	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000270	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000316	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000358	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000369	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000431	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000457	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0001177	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0005469	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0006101	ORPHA:2211	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000048	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000337	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000343	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000494	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000501	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000508	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000520	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000625	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0010059	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0011304	ORPHA:2211	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0000960	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0001302	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0001339	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0002084	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0002126	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0002269	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0002536	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0001302	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0008388	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2211	Hypertelorism-hypospadias-polysyndactyly syndrome		HP:0030769	ORPHA:2211	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000044	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000520	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000873	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000944	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000975	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001114	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001824	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001945	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001959	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002653	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002754	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002797	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0005930	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0011001	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0012378	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0100518	ORPHA:35687	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000126	ORPHA:35687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001386	ORPHA:35687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001646	ORPHA:35687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002027	ORPHA:35687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0005200	ORPHA:35687	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000083	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000505	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000508	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000639	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0000988	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001251	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001260	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001317	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001347	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001635	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001697	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0001903	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002017	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002094	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002202	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0002206	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0006530	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0010885	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0010978	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35687	Erdheim-Chester disease		HP:0012735	ORPHA:35687	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002141	ORPHA:210272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002172	ORPHA:210272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002317	ORPHA:210272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002321	ORPHA:210272	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0000496	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0000622	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0000651	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0000739	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0001289	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002013	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002018	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002076	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0002315	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0012378	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement		HP:0030826	ORPHA:210272	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement	NOT	HP:0007670	ORPHA:210272	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:210272	Mal de débarquement	NOT	HP:0410263	ORPHA:210272	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0003565	ORPHA:93552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0005421	ORPHA:93552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0045042	ORPHA:93552	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000079	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000083	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000093	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000100	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000123	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000790	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000951	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000969	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000988	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001698	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001873	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001882	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001888	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001937	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001945	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002202	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002716	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0003493	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0003613	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0011024	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0025435	ORPHA:93552	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000155	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000707	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0000709	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001250	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001324	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001369	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001541	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002013	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002027	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002086	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002094	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002301	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002315	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002725	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002829	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0003270	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0004372	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0007417	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0025300	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0025343	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0040319	ORPHA:93552	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0001596	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002014	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0002463	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0003453	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0030880	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0100543	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0100614	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93552	Pediatric systemic lupus erythematosus		HP:0100749	ORPHA:93552	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000219	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000252	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000316	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000319	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000490	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000653	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000750	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001166	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001249	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001252	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001265	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001270	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001337	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001508	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0004322	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0008551	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0009088	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0012368	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0012751	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0045075	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0045082	ORPHA:370079	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000722	ORPHA:370079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000729	ORPHA:370079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000739	ORPHA:370079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001263	ORPHA:370079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0007018	ORPHA:370079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0030800	ORPHA:370079	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000717	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000776	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0001250	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0002007	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0002650	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0007302	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0009553	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0009891	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0100753	ORPHA:370079	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0000054	ORPHA:370079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:370079	Proximal 16p11.2 microduplication syndrome		HP:0002937	ORPHA:370079	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2218	Cervical hypertrichosis-peripheral neuropathy syndrome		HP:0001305	ORPHA:2218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2218	Cervical hypertrichosis-peripheral neuropathy syndrome		HP:0002230	ORPHA:2218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2218	Cervical hypertrichosis-peripheral neuropathy syndrome		HP:0003457	ORPHA:2218	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2218	Cervical hypertrichosis-peripheral neuropathy syndrome		HP:0002754	ORPHA:2218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2218	Cervical hypertrichosis-peripheral neuropathy syndrome		HP:0040165	ORPHA:2218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2218	Cervical hypertrichosis-peripheral neuropathy syndrome		HP:0200042	ORPHA:2218	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002151	ORPHA:255182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002490	ORPHA:255182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0500231	ORPHA:255182	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0001250	ORPHA:255182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0001264	ORPHA:255182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0001273	ORPHA:255182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002273	ORPHA:255182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002928	ORPHA:255182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0003128	ORPHA:255182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0010915	ORPHA:255182	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0000252	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0001263	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0001274	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0001508	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002079	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002119	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002134	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0007109	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0008936	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0010864	ORPHA:255182	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0001317	ORPHA:255182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002059	ORPHA:255182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:255182	Pyruvate dehydrogenase E3-binding protein deficiency		HP:0002363	ORPHA:255182	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0000175	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0000252	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0001250	ORPHA:2216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0001252	ORPHA:2216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0001276	ORPHA:2216	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0001387	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0001511	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0002269	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0002353	ORPHA:2216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0004209	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0004322	ORPHA:2216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0007598	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0008056	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0008736	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0011800	ORPHA:2216	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2216	Maternal hyperthermia-induced birth defects		HP:0100543	ORPHA:2216	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0000079	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0000252	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0001561	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0001744	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0001789	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0002240	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0002269	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0002652	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0002813	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0003103	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0004322	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0006703	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0009826	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2204	Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type		HP:0011001	ORPHA:2204	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0025331	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0030051	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0031867	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0040288	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0045074	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0100022	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000252	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000708	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000736	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000750	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001249	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001250	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001263	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001987	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002161	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0003131	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0003268	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0003297	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0004322	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0008947	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0010850	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0012379	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0012403	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0012758	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0500163	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0500204	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0500208	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0500243	ORPHA:2203	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000218	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000319	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000457	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000486	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000601	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0000752	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001264	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001285	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001310	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001337	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001348	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001363	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001508	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0001999	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002013	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002015	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002020	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002033	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002179	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002311	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0002312	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0004971	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0006532	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0006889	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0008589	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0009739	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0011171	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0011342	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2203	Hyperlysinemia		HP:0011968	ORPHA:2203	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2202	Palmoplantar keratoderma-deafness syndrome		HP:0000407	ORPHA:2202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2202	Palmoplantar keratoderma-deafness syndrome		HP:0000962	ORPHA:2202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2202	Palmoplantar keratoderma-deafness syndrome		HP:0000982	ORPHA:2202	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0000982	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0001072	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0001231	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0001288	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0001761	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0003457	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0007021	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0008388	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0009830	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0010547	ORPHA:2201	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0001257	ORPHA:2201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2201	Palmoplantar keratoderma-spastic paralysis syndrome		HP:0002301	ORPHA:2201	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0000212	ORPHA:2200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0000222	ORPHA:2200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0000975	ORPHA:2200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0000982	ORPHA:2200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0001231	ORPHA:2200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0001597	ORPHA:2200	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0007497	ORPHA:2200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0008392	ORPHA:2200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2200	Focal palmoplantar and gingival keratoderma		HP:0008399	ORPHA:2200	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0002166	ORPHA:488333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0003474	ORPHA:488333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0007108	ORPHA:488333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0008959	ORPHA:488333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0009053	ORPHA:488333	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0001288	ORPHA:488333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0001348	ORPHA:488333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0001760	ORPHA:488333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0001761	ORPHA:488333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0003376	ORPHA:488333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0007002	ORPHA:488333	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0001765	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0003100	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0003438	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0006937	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0007328	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0008954	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0012531	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0030051	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:488333	Autosomal dominant Charcot-Marie-Tooth disease type 2W		HP:0030237	ORPHA:488333	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0000252	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0000518	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0000708	ORPHA:79254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0000716	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0000717	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0000964	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001010	ORPHA:79254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001250	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001263	ORPHA:79254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001268	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001276	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001337	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001347	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0001510	ORPHA:79254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0002017	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0002301	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0002333	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0002354	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0002514	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0004923	ORPHA:79254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0005599	ORPHA:79254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0007018	ORPHA:79254	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0010550	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0010864	ORPHA:79254	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0100679	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79254	Classic phenylketonuria		HP:0100716	ORPHA:79254	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001681	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002072	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002092	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0005244	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0006846	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0010885	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0012819	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0025326	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0100601	ORPHA:464343	TAS		HP:0040284			H	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0100758	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:3000042	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0003613	ORPHA:464343	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001977	ORPHA:464343	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001937	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002625	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002641	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002829	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0004420	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0004844	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0004936	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0005268	ORPHA:464343	TAS		HP:0040282			C	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0011112	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0020136	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0032376	ORPHA:464343	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0000707	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0000965	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001250	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001297	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001369	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001654	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001658	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0001873	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002076	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002204	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002326	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002638	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0002725	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0020137	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0025324	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0025343	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0031653	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0034084	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0034097	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0034098	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0034099	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0034100	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0034101	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0100576	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0100602	ORPHA:464343	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0200042	ORPHA:464343	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0000077	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464343	Catastrophic antiphospholipid syndrome		HP:0000726	ORPHA:464343	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001627	ORPHA:2209	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000252	ORPHA:2209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001249	ORPHA:2209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001263	ORPHA:2209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001511	ORPHA:2209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001680	ORPHA:2209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001999	ORPHA:2209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0004383	ORPHA:2209	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000218	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000343	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000347	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000431	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000463	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000752	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001250	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001629	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001636	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001719	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0002079	ORPHA:2209	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000286	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000340	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000486	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0000601	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001156	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0001488	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0002032	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0002836	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0004411	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0008589	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0009611	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0012210	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2209	Maternal phenylketonuria syndrome		HP:0030084	ORPHA:2209	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000455	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000768	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000926	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001007	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001072	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001230	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001250	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001789	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0008166	ORPHA:79255	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000365	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000618	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000707	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000924	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001249	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001263	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001433	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001999	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002376	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0003541	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0008947	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0410346	ORPHA:79255	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000943	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001257	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001638	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002267	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002506	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002652	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0007204	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0010729	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0011951	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0012753	ORPHA:79255	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000158	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000212	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000343	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000369	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0000400	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002007	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002684	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002690	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0002869	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0003026	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0004562	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0005280	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0006371	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0008479	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0008807	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0008812	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0011968	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0012307	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0025013	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0100767	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:3000050	ORPHA:79255	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79255	GM1 gangliosidosis type 1		HP:0001511	ORPHA:79255	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:2206	Ankylosing vertebral hyperostosis with tylosis		HP:0000925	ORPHA:2206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2206	Ankylosing vertebral hyperostosis with tylosis		HP:0002758	ORPHA:2206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2206	Ankylosing vertebral hyperostosis with tylosis		HP:0040163	ORPHA:2206	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:2206	Ankylosing vertebral hyperostosis with tylosis		HP:0000982	ORPHA:2206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:2206	Ankylosing vertebral hyperostosis with tylosis		HP:0001513	ORPHA:2206	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001510	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001538	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001943	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002149	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002155	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002240	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0003077	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0003124	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0003128	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0004322	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0006568	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0012379	ORPHA:79259	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000105	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000147	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000293	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000311	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000858	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000939	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001263	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001270	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001397	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001508	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001733	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002718	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0010974	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0100279	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0100512	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0100646	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0410252	ORPHA:79259	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000093	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000121	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000132	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000155	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000230	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000421	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000670	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000696	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000704	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000787	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000821	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000822	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000823	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000938	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0000978	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001114	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001892	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001903	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002014	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002037	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002173	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0002659	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0004387	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0005576	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0011890	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0012028	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0012146	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0030950	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0100543	ORPHA:79259	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001402	ORPHA:79259	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0001997	ORPHA:79259	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79259	Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib		HP:0003774	ORPHA:79259	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0000518	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0000952	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0001249	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0001252	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0001263	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0001510	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0001744	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0001824	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0002017	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0002240	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0003355	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0004915	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79238	Galactose epimerase deficiency		HP:0011968	ORPHA:79238	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000707	ORPHA:79239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0003251	ORPHA:79239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0012379	ORPHA:79239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0030272	ORPHA:79239	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000518	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000750	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000786	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000823	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000868	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000869	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000876	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000952	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001256	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001263	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001268	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001328	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001399	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001928	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002013	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002174	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002240	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002345	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002910	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0006977	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0008209	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0009088	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0012537	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0030353	ORPHA:79239	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000028	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000716	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000729	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000739	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0000939	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001250	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001251	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001254	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001260	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001288	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001298	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001332	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001943	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002014	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002141	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002311	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0002312	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0004349	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0007018	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0011098	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0011446	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0011968	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0020110	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0100512	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0100806	ORPHA:79239	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79239	Classic galactosemia		HP:0001541	ORPHA:79239	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:435804	Short stature-advanced bone age-early-onset osteoarthritis syndrome		HP:0001156	ORPHA:435804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435804	Short stature-advanced bone age-early-onset osteoarthritis syndrome		HP:0007281	ORPHA:435804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435804	Short stature-advanced bone age-early-onset osteoarthritis syndrome		HP:0009778	ORPHA:435804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435804	Short stature-advanced bone age-early-onset osteoarthritis syndrome		HP:0011800	ORPHA:435804	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:435804	Short stature-advanced bone age-early-onset osteoarthritis syndrome		HP:0002758	ORPHA:435804	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0000407	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0000974	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0001270	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0001382	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0001763	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0002421	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0002751	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0003198	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0003202	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0006829	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0007502	ORPHA:300179	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0000545	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0000938	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0000978	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0001075	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0001324	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0003236	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0003388	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0100790	ORPHA:300179	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0012372	ORPHA:300179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0025019	ORPHA:300179	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0000482	ORPHA:300179	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:300179	Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency		HP:0001519	ORPHA:300179	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:46348	Paroxysmal extreme pain disorder		HP:0001250	ORPHA:46348	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:46348	Paroxysmal extreme pain disorder		HP:0002019	ORPHA:46348	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0001410	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0001873	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0001903	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0001945	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0002960	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0003073	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0003281	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0003565	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0011118	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0012156	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0012649	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0025435	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0030356	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0011117	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0030783	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0031964	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0040089	ORPHA:158061	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0001744	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0001875	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0002155	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0002716	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0005681	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0011227	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0011900	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0031956	ORPHA:158061	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0001298	ORPHA:158061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0002240	ORPHA:158061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0002725	ORPHA:158061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158061	Macrophage activation syndrome		HP:0012115	ORPHA:158061	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002155	ORPHA:79240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002240	ORPHA:79240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0008897	ORPHA:79240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0012379	ORPHA:79240	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001395	ORPHA:79240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002910	ORPHA:79240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003124	ORPHA:79240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003162	ORPHA:79240	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0000147	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0000750	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0000858	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0000876	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001252	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001394	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001744	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001947	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001988	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002194	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002719	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003202	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003236	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003323	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003325	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003326	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003394	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003546	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003749	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0004322	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0011342	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0012378	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0012734	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0100607	ORPHA:79240	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0000939	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001402	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0001903	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002013	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002014	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002018	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0002913	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003128	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0003201	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0004324	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79240	Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency		HP:0012028	ORPHA:79240	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001992	ORPHA:79241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0005979	ORPHA:79241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0410145	ORPHA:79241	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000407	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000707	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000988	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001250	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001252	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001987	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002715	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0410263	ORPHA:79241	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000365	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000478	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000509	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000575	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000648	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0000964	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001138	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001249	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001251	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001254	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001263	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0001596	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002069	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002098	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002104	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002123	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002196	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002313	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002841	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0002883	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0003690	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0004429	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0005401	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0006511	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0011153	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0012469	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79241	Biotinidase deficiency		HP:0200068	ORPHA:79241	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0000737	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001096	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001250	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001252	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001510	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001824	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0002017	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0002039	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0011127	ORPHA:79242	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001987	ORPHA:79242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001992	ORPHA:79242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0002098	ORPHA:79242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0002789	ORPHA:79242	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0000964	ORPHA:79242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001251	ORPHA:79242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001254	ORPHA:79242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001259	ORPHA:79242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001596	ORPHA:79242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0001873	ORPHA:79242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79242	Holocarboxylase synthetase deficiency		HP:0007549	ORPHA:79242	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001518	ORPHA:79243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002151	ORPHA:79243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002490	ORPHA:79243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0500231	ORPHA:79243	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0000707	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001250	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001511	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001999	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002059	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002069	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002119	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002171	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002187	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0003128	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0003542	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0004902	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0006956	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0011193	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0011196	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0011199	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0012443	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0025361	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0030917	ORPHA:79243	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0000252	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0000618	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0000954	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001251	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001252	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001274	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001332	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001338	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001371	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001629	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001761	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0001883	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002020	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002079	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002100	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002126	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002329	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002350	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002521	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002540	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002643	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0002719	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0006799	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0006970	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0006999	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0009826	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0010576	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0011471	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0011968	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0012128	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0012469	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79243	Pyruvate dehydrogenase E1-alpha deficiency		HP:0012698	ORPHA:79243	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0001288	ORPHA:79244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0012379	ORPHA:79244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0100503	ORPHA:79244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0500231	ORPHA:79244	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000496	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000546	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000707	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000708	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0001260	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0001263	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0001276	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0001288	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0002136	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0002180	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0002268	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0002395	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0002454	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0003487	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0005656	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0010864	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0025331	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0025335	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0031139	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0031936	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0031960	ORPHA:79244	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000252	ORPHA:79244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000486	ORPHA:79244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000726	ORPHA:79244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0000739	ORPHA:79244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0004302	ORPHA:79244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0007994	ORPHA:79244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79244	Pyruvate dehydrogenase E2 deficiency		HP:0011098	ORPHA:79244	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0000316	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0000369	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0000463	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0000470	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0000924	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001156	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001250	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001508	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001799	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001999	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0002311	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0002650	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0002656	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0002808	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0008093	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0011344	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0011800	ORPHA:420794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001338	ORPHA:420794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001561	ORPHA:420794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0005792	ORPHA:420794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0006385	ORPHA:420794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0012537	ORPHA:420794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0000943	ORPHA:420794	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0001252	ORPHA:420794	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0010230	ORPHA:420794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:420794	Cono-spondylar dysplasia		HP:0010864	ORPHA:420794	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0002928	ORPHA:79246	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0001319	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0002151	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0003128	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0003348	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0003648	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0008358	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0008936	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0011342	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0040328	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79246	Pyruvate dehydrogenase phosphatase deficiency		HP:0410263	ORPHA:79246	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0001257	ORPHA:35689	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0002127	ORPHA:35689	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0002493	ORPHA:35689	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0003487	ORPHA:35689	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0007034	ORPHA:35689	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0002015	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0002064	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0002200	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0002371	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0002464	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0003444	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0007199	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0010549	ORPHA:35689	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0006827	ORPHA:35689	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0007002	ORPHA:35689	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis		HP:0010873	ORPHA:35689	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis	NOT	HP:0002366	ORPHA:35689	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:35689	Primary lateral sclerosis	NOT	HP:0003474	ORPHA:35689	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000967	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000979	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001433	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001622	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001789	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001873	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001978	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0006267	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0040165	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0040186	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0040188	ORPHA:499009	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000100	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000218	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000365	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000491	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000501	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000518	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000554	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001511	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001733	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001903	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0002007	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0002014	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0002024	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0002090	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0002716	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0006579	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0011092	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0012229	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0012384	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0012413	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0012424	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0012758	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0012819	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0025524	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0033782	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0100769	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0430028	ORPHA:499009	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000238	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0000648	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001250	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001287	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0001943	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0002982	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0006824	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:499009	Congenital syphilis		HP:0011120	ORPHA:499009	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002910	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0004377	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0011900	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0025435	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001399	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001433	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002863	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002922	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0004808	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0005521	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0006721	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0006775	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0012189	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0012190	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0012191	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0012229	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0020072	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0030080	ORPHA:158057	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001402	ORPHA:158057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002667	ORPHA:158057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002860	ORPHA:158057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0003003	ORPHA:158057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0012125	ORPHA:158057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0100526	ORPHA:158057	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0012156	ORPHA:158057	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001744	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001876	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001945	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002958	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0003281	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0011227	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0012211	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0011117	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0040218	ORPHA:158057	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001873	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001875	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0001903	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002155	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:158057	Acquired hemophagocytic lymphohistiocytosis associated with malignant disease		HP:0002904	ORPHA:158057	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002086	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002094	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002797	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0011842	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0011900	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0012735	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0025408	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0000421	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0000464	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0000782	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0000978	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001433	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001737	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001744	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001873	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001945	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002823	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0003084	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0003174	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0003312	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0003319	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0003546	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0005107	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0005562	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0011896	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0031095	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0031364	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0040163	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0100310	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0100608	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0100711	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0100749	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0100764	ORPHA:464329	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0000105	ORPHA:464329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001903	ORPHA:464329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002105	ORPHA:464329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002693	ORPHA:464329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0012740	ORPHA:464329	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002088	ORPHA:464329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0002202	ORPHA:464329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0045026	ORPHA:464329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0100763	ORPHA:464329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0100766	ORPHA:464329	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0000765	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001698	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464329	Kaposiform lymphangiomatosis		HP:0001892	ORPHA:464329	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0000135	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0000802	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0000819	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0000939	ORPHA:79230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0001254	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0001324	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0001644	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0002612	ORPHA:79230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0002910	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0003040	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0003281	ORPHA:79230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0007440	ORPHA:79230	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0011031	ORPHA:79230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0012093	ORPHA:79230	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79230	HJV or HAMP-related hemochromatosis		HP:0012463	ORPHA:79230	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001873	ORPHA:464321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002239	ORPHA:464321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0011121	ORPHA:464321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0012718	ORPHA:464321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0025015	ORPHA:464321	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002088	ORPHA:464321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002170	ORPHA:464321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0011354	ORPHA:464321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0025474	ORPHA:464321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0030350	ORPHA:464321	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0000077	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0000478	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0000759	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001250	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001342	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001392	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001627	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002011	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002105	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002248	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002249	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002573	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002797	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002904	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0003304	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0009139	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0011035	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0012735	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0012758	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0031368	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0045039	ORPHA:464321	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0000573	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001541	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001639	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0001945	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002134	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0002514	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0003273	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0007902	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0009830	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0010536	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0025064	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0025085	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0025420	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0031938	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:464321	Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome		HP:0040242	ORPHA:464321	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0000112	ORPHA:79233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0001249	ORPHA:79233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0001332	ORPHA:79233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0002149	ORPHA:79233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0003149	ORPHA:79233	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0000083	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0000707	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0000791	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0001250	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0001263	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0001347	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0001919	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0001997	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0002071	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0003259	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0012587	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency		HP:0100518	ORPHA:79233	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79233	Hypoxanthine guanine phosphoribosyltransferase partial deficiency	NOT	HP:0000742	ORPHA:79233	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0000365	ORPHA:79234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0000750	ORPHA:79234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0001080	ORPHA:79234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0001249	ORPHA:79234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0001250	ORPHA:79234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0001337	ORPHA:79234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0001343	ORPHA:79234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0001392	ORPHA:79234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0002354	ORPHA:79234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0003265	ORPHA:79234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0006579	ORPHA:79234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0008282	ORPHA:79234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0008947	ORPHA:79234	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79234	Crigler-Najjar syndrome type 1		HP:0012246	ORPHA:79234	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79235	Crigler-Najjar syndrome type 2		HP:0003265	ORPHA:79235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79235	Crigler-Najjar syndrome type 2		HP:0006579	ORPHA:79235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79235	Crigler-Najjar syndrome type 2		HP:0008282	ORPHA:79235	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0012024	ORPHA:79237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0012379	ORPHA:79237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0410061	ORPHA:79237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0410062	ORPHA:79237	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0000518	ORPHA:79237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0100018	ORPHA:79237	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0000815	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0000842	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001249	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001270	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001433	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001518	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0002240	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0008209	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0011098	ORPHA:79237	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0000252	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0000407	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001250	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001508	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001622	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0001943	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0002361	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0003124	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0004431	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0011968	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79237	Galactokinase deficiency		HP:0012768	ORPHA:79237	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0000083	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0000613	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0000708	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0000975	ORPHA:83317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0000988	ORPHA:83317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0001250	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0001254	ORPHA:83317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0001287	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0001337	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0001744	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0001892	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0001945	ORPHA:83317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002017	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002027	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002091	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002094	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002315	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002383	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002615	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0002716	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0003326	ORPHA:83317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0004372	ORPHA:83317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0012122	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0012733	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0012735	ORPHA:83317	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0012819	ORPHA:83317	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83317	Scrub typhus		HP:0100758	ORPHA:83317	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000359	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000407	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000512	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000518	ORPHA:231178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000545	ORPHA:231178	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000572	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000575	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000639	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000662	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000670	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000682	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000691	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000716	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000738	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0000739	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0001251	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0002120	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0007360	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0007730	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0011073	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0012157	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0012377	ORPHA:231178	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231178	Usher syndrome type 2		HP:0100753	ORPHA:231178	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0000988	ORPHA:83313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0001945	ORPHA:83313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0040211	ORPHA:83313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0100872	ORPHA:83313	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0000083	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0001873	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002315	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002716	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002829	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002910	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0003326	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0003496	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0012733	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0025289	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0032156	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0040186	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0200036	ORPHA:83313	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0000967	ORPHA:83313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0001882	ORPHA:83313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002014	ORPHA:83313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002018	ORPHA:83313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002027	ORPHA:83313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0003237	ORPHA:83313	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0000613	ORPHA:83313	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002633	ORPHA:83313	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:83313	Boutonneuse fever		HP:0002878	ORPHA:83313	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001987	ORPHA:247525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0011966	ORPHA:247525	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001399	ORPHA:247525	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0000707	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001250	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001254	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001257	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001508	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001950	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002013	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002342	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002480	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0006889	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0011968	ORPHA:247525	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0000473	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0000575	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001251	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001252	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001256	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001259	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0001350	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002020	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002076	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002315	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002516	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0002789	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0007185	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:247525	Citrullinemia type I		HP:0011448	ORPHA:247525	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001249	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001263	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001382	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0003160	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0004474	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0005328	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0007392	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0011003	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0025082	ORPHA:357058	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000023	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000260	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000270	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000426	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000486	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000494	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001252	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001302	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001511	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001763	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002197	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002198	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002376	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002384	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002438	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0005272	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0005445	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0005484	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0006891	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0008897	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0011344	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0011451	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0100874	ORPHA:357058	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000343	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000592	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001250	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001251	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001257	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001305	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001320	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001332	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001350	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001374	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0001892	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002007	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002305	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002334	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002540	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0006989	ORPHA:357058	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000365	ORPHA:357058	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0000481	ORPHA:357058	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A		HP:0002659	ORPHA:357058	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A	NOT	HP:0000974	ORPHA:357058	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:357058	Autosomal recessive cutis laxa type 2A	NOT	HP:0007957	ORPHA:357058	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0004326	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0009931	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0010804	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0011968	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0100660	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0100963	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0200055	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000470	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000639	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001511	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002079	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002360	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002510	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002870	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002987	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0003273	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0003458	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0006380	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0008936	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0011470	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0100024	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0100716	ORPHA:371364	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000486	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000565	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000750	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001263	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001270	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001344	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0008947	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0009884	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0010864	ORPHA:371364	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000219	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000252	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000319	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000322	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000325	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000347	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000358	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000426	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000431	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000463	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0000494	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001166	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001250	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001252	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001319	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001357	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001525	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001762	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0001999	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002007	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002019	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002353	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0002650	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:371364	Hypotonia-speech impairment-severe cognitive delay syndrome		HP:0004322	ORPHA:371364	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000218	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000316	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000347	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000938	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0002148	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0002150	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0002515	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0002694	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0002753	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0003072	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0003080	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0003155	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0006487	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0008873	ORPHA:33067	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000121	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000293	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000494	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000520	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0000883	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0002643	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0008872	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0010537	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0034392	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type		HP:0200138	ORPHA:33067	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33067	Metaphyseal chondrodysplasia, Jansen type	NOT	HP:0003165	ORPHA:33067	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002376	ORPHA:33069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0007240	ORPHA:33069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0007359	ORPHA:33069	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0000466	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0000729	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0000739	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0001300	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0001327	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0001336	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002063	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002067	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002123	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002349	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002373	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002384	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002396	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0006813	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0007207	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0007270	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0008770	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0010841	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0011169	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0011172	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0011182	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0011468	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0012847	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0100543	ORPHA:33069	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0000736	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0000980	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0001763	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002283	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002307	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002311	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0002345	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0003066	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0007010	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0008081	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0008947	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0011185	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0011198	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0025101	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0031475	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0100694	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0100710	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0200048	ORPHA:33069	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:33069	Dravet syndrome		HP:0010818	ORPHA:33069	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93599	Primary hyperoxaluria type 2		HP:0000121	ORPHA:93599	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93599	Primary hyperoxaluria type 2		HP:0000787	ORPHA:93599	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93599	Primary hyperoxaluria type 2		HP:0003159	ORPHA:93599	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93599	Primary hyperoxaluria type 2		HP:0000010	ORPHA:93599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93599	Primary hyperoxaluria type 2		HP:0006000	ORPHA:93599	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93599	Primary hyperoxaluria type 2		HP:0000083	ORPHA:93599	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0100518	ORPHA:93598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0000010	ORPHA:93598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0000805	ORPHA:93598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0000121	ORPHA:93598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0000787	ORPHA:93598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0001903	ORPHA:93598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0001942	ORPHA:93598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0003159	ORPHA:93598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0003761	ORPHA:93598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0011021	ORPHA:93598	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0000790	ORPHA:93598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0001508	ORPHA:93598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0012213	ORPHA:93598	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0000924	ORPHA:93598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0003774	ORPHA:93598	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0000164	ORPHA:93598	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0001297	ORPHA:93598	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0001939	ORPHA:93598	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:93598	Primary hyperoxaluria type 1		HP:0002621	ORPHA:93598	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001252	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001274	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001999	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0002683	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0002928	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0003128	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0004325	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0012758	ORPHA:255138	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001250	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001251	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001302	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001315	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001321	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0001511	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0002079	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0002119	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0002365	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0006970	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0007016	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0007109	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0007165	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0007772	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency		HP:0200012	ORPHA:255138	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0010873	ORPHA:363722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0011441	ORPHA:363722	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0000639	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0001251	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0001257	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0001260	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0001347	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0001618	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0002015	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0002313	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0002518	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0002839	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0003487	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0003690	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0007109	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0010530	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0012332	ORPHA:363722	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0002063	ORPHA:363722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0002360	ORPHA:363722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363722	Alexander disease type II		HP:0002650	ORPHA:363722	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0002460	ORPHA:357043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0003202	ORPHA:357043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0003487	ORPHA:357043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0007256	ORPHA:357043	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0001258	ORPHA:357043	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0001288	ORPHA:357043	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0001761	ORPHA:357043	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357043	Amyotrophic lateral sclerosis type 4		HP:0003474	ORPHA:357043	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0001511	ORPHA:1797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0002650	ORPHA:1797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0003422	ORPHA:1797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0003510	ORPHA:1797	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000269	ORPHA:1797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000431	ORPHA:1797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000463	ORPHA:1797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000470	ORPHA:1797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000582	ORPHA:1797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0003307	ORPHA:1797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0010306	ORPHA:1797	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000008	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000175	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000252	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000256	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000772	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000913	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0000921	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0002205	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0003298	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0005107	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1797	Autosomal dominant spondylocostal dysostosis		HP:0030680	ORPHA:1797	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000161	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000164	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000175	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000347	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000366	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000430	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000431	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000492	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000499	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0000582	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0001156	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0001181	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0002006	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0031095	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0004322	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0007957	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0008056	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0100490	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0100543	ORPHA:1794	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0100840	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1794	Oculomaxillofacial dysostosis		HP:0200102	ORPHA:1794	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0002500	ORPHA:363717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0007183	ORPHA:363717	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001250	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001272	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001508	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0002650	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0004481	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0007256	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0012696	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0100320	ORPHA:363717	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0000238	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001251	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001257	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001260	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001263	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001347	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0002015	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0004326	ORPHA:363717	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001252	ORPHA:363717	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0001290	ORPHA:363717	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0002013	ORPHA:363717	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:363717	Alexander disease type I		HP:0010530	ORPHA:363717	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0000505	ORPHA:79292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0001681	ORPHA:79292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0001744	ORPHA:79292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0002240	ORPHA:79292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0002621	ORPHA:79292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0002716	ORPHA:79292	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0003233	ORPHA:79292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79292	Fish-eye disease		HP:0007957	ORPHA:79292	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000175	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000248	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000316	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000337	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000384	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000453	ORPHA:1791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000456	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000457	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000482	ORPHA:1791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000506	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000508	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000518	ORPHA:1791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000568	ORPHA:1791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000581	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000612	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0000636	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0001088	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0001140	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0001482	ORPHA:1791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0002006	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0002079	ORPHA:1791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0002084	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0003196	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0004132	ORPHA:1791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0004322	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0005280	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0007036	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0007708	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0011800	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0100335	ORPHA:1791	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1791	Frontofacionasal dysplasia		HP:0100840	ORPHA:1791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000008	ORPHA:1790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000160	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000175	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000193	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000243	ORPHA:1790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000248	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000369	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000452	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000463	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000494	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000520	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000582	ORPHA:1790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0000588	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0001363	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0001522	ORPHA:1790	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0001561	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0001631	ORPHA:1790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0001643	ORPHA:1790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0002205	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0002777	ORPHA:1790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0003196	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0005439	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0005607	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0008749	ORPHA:1790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0010295	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0011800	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1790	Hypomandibular faciocranial dysostosis		HP:0100543	ORPHA:1790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0000979	ORPHA:93585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001873	ORPHA:93585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001937	ORPHA:93585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:6000462	ORPHA:93585	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0000093	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0000790	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001250	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001259	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001289	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001297	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001324	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001923	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001945	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001981	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002014	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002018	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002027	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002094	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002315	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002829	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002904	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0003326	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0003419	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0008282	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0012378	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0020181	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0025435	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0033404	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0410173	ORPHA:93585	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0000651	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001635	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001645	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001658	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0001919	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0002381	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0003115	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0003138	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0003259	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0011675	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0030149	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:93585	Immune-mediated thrombotic thrombocytopenic purpura		HP:0100749	ORPHA:93585	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0000825	ORPHA:79299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0001985	ORPHA:79299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0001988	ORPHA:79299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0008283	ORPHA:79299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0030794	ORPHA:79299	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0001250	ORPHA:79299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0001324	ORPHA:79299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0002378	ORPHA:79299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0012378	ORPHA:79299	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0001259	ORPHA:79299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0005978	ORPHA:79299	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0002270	ORPHA:79299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79299	Congenital glucokinase-related hyperinsulinism		HP:0012638	ORPHA:79299	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000375	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000407	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000483	ORPHA:231183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000512	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000518	ORPHA:231183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000572	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000575	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000662	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000716	ORPHA:231183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000738	ORPHA:231183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0000739	ORPHA:231183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0001251	ORPHA:231183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0001756	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0007730	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0008499	ORPHA:231183	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0012377	ORPHA:231183	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231183	Usher syndrome type 3		HP:0100753	ORPHA:231183	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002751	ORPHA:536471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002761	ORPHA:536471	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000164	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000316	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000325	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000358	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000369	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000520	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000592	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000926	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000938	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000946	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000963	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000974	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000977	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001027	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001167	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001252	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001263	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001371	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001373	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001382	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001385	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001762	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001763	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001999	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002007	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002650	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002659	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002828	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003468	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0004322	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0004993	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0008453	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0012368	ORPHA:536471	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000160	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000175	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000337	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000343	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000347	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000365	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000463	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000494	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000894	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000954	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000973	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001075	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001270	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001654	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001772	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002093	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002209	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002974	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002987	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003015	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003016	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003048	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003196	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003368	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003370	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0004568	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0005280	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0006487	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0008499	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0009811	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0010575	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0011332	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0011341	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0040160	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0100255	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0100864	ORPHA:536471	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000023	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000028	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000135	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000485	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000486	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000501	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000508	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000545	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000588	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000609	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000612	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0000768	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001004	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001043	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001054	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001631	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001642	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001650	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0001822	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002089	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002091	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0002999	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0003417	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0004269	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0004442	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0004970	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0007787	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0007957	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0008807	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0009944	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0010754	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0012687	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0040047	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:536471	Spondylodysplastic Ehlers-Danlos syndrome		HP:0100777	ORPHA:536471	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1799	Familial developmental dysphasia		HP:0002381	ORPHA:1799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1799	Familial developmental dysphasia		HP:0002474	ORPHA:1799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1799	Familial developmental dysphasia		HP:0002546	ORPHA:1799	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319600	Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency		HP:0001945	ORPHA:319600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319600	Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency		HP:0002716	ORPHA:319600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:319600	Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency		HP:0010978	ORPHA:319600	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000158	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000164	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000174	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000248	ORPHA:1798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000252	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000316	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000327	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000444	ORPHA:1798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000446	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000470	ORPHA:1798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000520	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000670	ORPHA:1798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000682	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000767	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000929	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0000944	ORPHA:1798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0001156	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0002514	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0002645	ORPHA:1798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0002650	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0002652	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0002808	ORPHA:1798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0002983	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0003307	ORPHA:1798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0004322	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0004474	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0005105	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0005665	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0005930	ORPHA:1798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0006487	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0009804	ORPHA:1798	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0010669	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0011001	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0011800	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0012368	ORPHA:1798	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1798	Craniofacial dysostosis-diaphyseal hyperplasia syndrome		HP:0100777	ORPHA:1798	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0001744	ORPHA:231154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0001890	ORPHA:231154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0001904	ORPHA:231154	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0002721	ORPHA:231154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0002960	ORPHA:231154	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0004430	ORPHA:231154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0005403	ORPHA:231154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0006515	ORPHA:231154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0010976	ORPHA:231154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231154	Combined immunodeficiency due to partial RAG1 deficiency		HP:0100806	ORPHA:231154	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0000848	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0001278	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0001945	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0002013	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0002153	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0002615	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0002902	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0004319	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0012112	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0012606	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0025436	ORPHA:556037	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0001508	ORPHA:556037	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism		HP:0008897	ORPHA:556037	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:556037	Late-onset familial hypoaldosteronism	NOT	HP:0000811	ORPHA:556037	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0001904	ORPHA:464370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0003453	ORPHA:464370	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0002090	ORPHA:464370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0032169	ORPHA:464370	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0000952	ORPHA:464370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0001287	ORPHA:464370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0001945	ORPHA:464370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0005268	ORPHA:464370	TAS		HP:0040283			C	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0005968	ORPHA:464370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0009800	ORPHA:464370	TAS		HP:0040283			H	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0032435	ORPHA:464370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:464370	Neonatal alloimmune neutropenia		HP:0100806	ORPHA:464370	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000358	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000369	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000938	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001027	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001382	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002007	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002651	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002751	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002757	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002828	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003016	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0004993	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0005008	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0006487	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0008807	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0008897	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0010575	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0011800	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0012095	ORPHA:536467	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000218	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000238	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000343	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000347	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000463	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000520	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000592	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000691	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000939	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000963	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000974	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000978	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001075	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001166	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001181	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001252	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001270	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001319	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001385	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001762	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001822	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003196	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003300	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0004568	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0005280	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0006243	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0010646	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0010648	ORPHA:536467	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000410	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000473	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000482	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000501	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000545	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000670	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000703	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000750	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000767	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000768	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000926	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0000946	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001250	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001297	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001357	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001363	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001562	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0001634	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002089	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002091	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002093	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002098	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002616	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002650	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002779	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0002974	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0003414	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0004970	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0005678	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0006522	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0008453	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0009726	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0012366	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0012727	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0100750	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:536467	B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome		HP:0500087	ORPHA:536467	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001476	ORPHA:357074	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000218	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000253	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000272	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000316	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000319	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000343	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000369	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000455	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000463	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000494	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000670	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000726	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000750	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000973	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001263	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001270	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001508	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001511	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001582	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0002187	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0002208	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0002361	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0002465	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0002761	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0003160	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0003196	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0003199	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0004322	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0005272	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0005989	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0006891	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0007392	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0007457	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0007552	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0008070	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0008897	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0008947	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0009125	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0011003	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0011968	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0025167	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0100874	ORPHA:357074	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000023	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0000486	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001250	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001257	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001302	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001305	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001321	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001339	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0001374	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0002126	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0025201	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0025244	ORPHA:357074	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		HP:0010989	ORPHA:357074	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type	NOT	HP:0002097	ORPHA:357074	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000023	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000028	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000047	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000164	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000174	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000252	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000308	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000319	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000348	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000358	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000465	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000494	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000670	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0000767	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0001156	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0001256	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0001511	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0001622	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0002006	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0002208	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0002750	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0003196	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0003298	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0004209	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0004279	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0004322	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0004467	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0006101	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0007477	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0007598	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0008872	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0009804	ORPHA:1786	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0010669	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0010720	ORPHA:1786	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1786	Acrofacial dysostosis, Catania type		HP:0200055	ORPHA:1786	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001249	ORPHA:592574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0008872	ORPHA:592574	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000028	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000164	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000252	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000286	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000288	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000316	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000365	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000369	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000463	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000486	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000506	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000508	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000527	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000540	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000729	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001270	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001511	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001852	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0002000	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0002553	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0002788	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0003196	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0005280	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0011220	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0200006	ORPHA:592574	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000023	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000175	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0000545	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001250	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001385	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001518	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001537	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0001627	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0002650	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0004209	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0004322	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0010935	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0012725	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0025502	ORPHA:592574	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0002926	ORPHA:592574	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0012762	ORPHA:592574	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:592574	Menke-Hennekam syndrome		HP:0034323	ORPHA:592574	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000047	ORPHA:1784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000048	ORPHA:1784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000119	ORPHA:1784	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000175	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000218	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000232	ORPHA:1784	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000248	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000316	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000337	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000455	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000494	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000508	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0000625	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0001053	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0001088	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0001156	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0001798	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0002120	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0002983	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0004132	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0004322	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0005930	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0009882	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0010864	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0011304	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0011800	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0100335	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0100490	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1784	Acrofrontofacionasal dysostosis		HP:0100840	ORPHA:1784	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0000214	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0000280	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0000360	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0000365	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0000962	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0001004	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0001071	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0001256	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0001482	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0001640	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0002321	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0005280	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0007428	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0007759	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0009830	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0012471	ORPHA:79280	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0100585	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79280	Alpha-N-acetylgalactosaminidase deficiency type 2		HP:0200034	ORPHA:79280	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000256	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000316	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000365	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000639	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000648	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000682	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000684	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000926	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0000944	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0001249	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0001291	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0001629	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0002376	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0002514	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0002757	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0003301	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0004322	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0004493	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0008065	ORPHA:1782	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0008479	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0011001	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1782	Dysosteosclerosis		HP:0100670	ORPHA:1782	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0000486	ORPHA:79281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0000518	ORPHA:79281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0000717	ORPHA:79281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0001249	ORPHA:79281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0001250	ORPHA:79281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0001263	ORPHA:79281	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0001639	ORPHA:79281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79281	Alpha-N-acetylgalactosaminidase deficiency type 3		HP:0002240	ORPHA:79281	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001249	ORPHA:79282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001889	ORPHA:79282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002160	ORPHA:79282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002912	ORPHA:79282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0012120	ORPHA:79282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0031544	ORPHA:79282	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000206	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000252	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000505	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000546	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000580	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000639	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000648	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001116	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001508	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001510	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001873	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0008002	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0010280	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0011968	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0100820	ORPHA:79282	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000083	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000707	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000708	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000751	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000952	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001250	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001251	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001252	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001254	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001268	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001298	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001511	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001627	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001644	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001789	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001875	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001907	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001943	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001944	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001987	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002045	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002059	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002092	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002098	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002167	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002352	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002354	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002625	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002919	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0003658	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0006827	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0007010	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0008765	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0011096	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0012469	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0012758	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0030891	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0033051	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0100309	ORPHA:79282	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000238	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000276	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000319	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000348	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000369	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000709	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0000726	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001297	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001942	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0001999	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002204	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0002376	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0005575	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0007258	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0012443	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79282	Methylmalonic acidemia with homocystinuria, type cblC		HP:0031258	ORPHA:79282	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000126	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000143	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000160	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000316	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000358	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000400	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000414	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000463	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000465	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000470	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000582	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000637	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0000776	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0001252	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0001274	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0001334	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0001511	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0001629	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0001636	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0001669	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0002023	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0002575	ORPHA:1780	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0002714	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0002937	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1780	Thakker-Donnai syndrome		HP:0004602	ORPHA:1780	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0000708	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0000980	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0001249	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0001250	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0001254	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0001263	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0001288	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0001508	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0001980	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0002039	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0012378	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79283	Methylmalonic acidemia with homocystinuria, type cblD		HP:0100022	ORPHA:79283	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0000219	ORPHA:370010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0000455	ORPHA:370010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0000750	ORPHA:370010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0001328	ORPHA:370010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0002342	ORPHA:370010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0011822	ORPHA:370010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0012745	ORPHA:370010	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0000252	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0000273	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0000403	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0000954	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0001156	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0001800	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0001831	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0001965	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0001288	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0002465	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0003484	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0004322	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0004602	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0009611	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0009644	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0009648	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0009650	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0009778	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0009882	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0010041	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0010047	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0010492	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0011304	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0011939	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0012553	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0012713	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370010	Intellectual disability-facial dysmorphism-hand anomalies syndrome		HP:0025502	ORPHA:370010	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001889	ORPHA:79284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0002160	ORPHA:79284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0003145	ORPHA:79284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0003223	ORPHA:79284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0012120	ORPHA:79284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0031544	ORPHA:79284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0100502	ORPHA:79284	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001249	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001250	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001252	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001254	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001508	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001510	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001511	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001627	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001999	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0002719	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0011968	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0012758	ORPHA:79284	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0000122	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0000175	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0000206	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0000988	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0001875	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0006571	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0010280	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF		HP:0030746	ORPHA:79284	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79284	Methylmalonic acidemia with homocystinuria type cblF	NOT	HP:0003658	ORPHA:79284	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0001508	ORPHA:556030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0002153	ORPHA:556030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0002615	ORPHA:556030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0002902	ORPHA:556030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0008897	ORPHA:556030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0012606	ORPHA:556030	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0000848	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0001278	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0001290	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0001944	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0002013	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0004319	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0011968	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0012112	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism		HP:0025436	ORPHA:556030	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:556030	Early-onset familial hypoaldosteronism	NOT	HP:0000811	ORPHA:556030	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0000272	ORPHA:1788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0000308	ORPHA:1788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0000426	ORPHA:1788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0009380	ORPHA:1788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0008551	ORPHA:1788	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0000912	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0002139	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0002410	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0002644	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0002974	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0003038	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0006495	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0006501	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0030680	ORPHA:1788	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0000130	ORPHA:1788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0001511	ORPHA:1788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0001762	ORPHA:1788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0003312	ORPHA:1788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0006101	ORPHA:1788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1788	Acrofacial dysostosis, Rodríguez type		HP:0008678	ORPHA:1788	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0002650	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0002705	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0003298	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0003777	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0004334	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0008065	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0100333	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000294	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000347	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000358	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000369	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000653	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000677	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0002750	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0004322	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0005338	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0006101	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0010044	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0011800	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0200055	ORPHA:1787	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000272	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000337	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000414	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000470	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0003312	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0008070	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0011069	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0045074	ORPHA:1787	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1787	Acrofacial dysostosis, Palagonia type		HP:0000492	ORPHA:1787	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0030781	ORPHA:26793	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0000952	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001518	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001629	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001631	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001655	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001985	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002045	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002098	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002240	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002876	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002910	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0003236	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0009045	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0011968	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0025502	ORPHA:26793	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0000256	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001254	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001513	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001545	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001644	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001649	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001657	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001663	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001678	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001698	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001942	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0001987	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002013	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002090	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002280	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002789	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0002901	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0003075	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0003394	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0004756	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0008947	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0011123	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0011675	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26793	Very long chain acyl-CoA dehydrogenase deficiency		HP:0012531	ORPHA:26793	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000375	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000407	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000512	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000518	ORPHA:231169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000572	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000575	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000662	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000682	ORPHA:231169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000716	ORPHA:231169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000738	ORPHA:231169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0000739	ORPHA:231169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0001249	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0001251	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0001263	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0001756	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0002120	ORPHA:231169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0007360	ORPHA:231169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0007730	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0008499	ORPHA:231169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0012157	ORPHA:231169	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0012377	ORPHA:231169	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231169	Usher syndrome type 1		HP:0100753	ORPHA:231169	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000135	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000480	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000518	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000568	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000639	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0001249	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0001513	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0003241	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0012758	ORPHA:363741	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000028	ORPHA:363741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000510	ORPHA:363741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0000771	ORPHA:363741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0006889	ORPHA:363741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:363741	Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome		HP:0100702	ORPHA:363741	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0000975	ORPHA:29822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0000980	ORPHA:29822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0000988	ORPHA:29822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0001250	ORPHA:29822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0001251	ORPHA:29822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0001288	ORPHA:29822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0001337	ORPHA:29822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0002014	ORPHA:29822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0002017	ORPHA:29822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0002045	ORPHA:29822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0002360	ORPHA:29822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0002793	ORPHA:29822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0004372	ORPHA:29822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0007370	ORPHA:29822	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0011675	ORPHA:29822	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:29822	Spontaneous periodic hypothermia		HP:0012378	ORPHA:29822	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000303	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000327	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000484	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000508	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000565	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000581	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0001047	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0001256	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0001513	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0001822	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0006333	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0006897	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0010164	ORPHA:397973	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000256	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000486	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000506	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000729	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0000752	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0001609	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0002187	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0002690	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0007663	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0011344	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0100046	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0100057	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0100068	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:397973	Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome		HP:0100271	ORPHA:397973	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0000252	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0000369	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0000601	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0000750	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001249	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001258	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001260	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001263	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001347	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001508	ORPHA:477673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0002136	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0002307	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001288	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0003487	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0006829	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0011470	ORPHA:477673	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0000341	ORPHA:477673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001250	ORPHA:477673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0001337	ORPHA:477673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0002079	ORPHA:477673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0002373	ORPHA:477673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:477673	Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome		HP:0011400	ORPHA:477673	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0001541	ORPHA:26790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0001824	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0002017	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0002019	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0002027	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0002037	ORPHA:26790	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0002093	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0002585	ORPHA:26790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0002716	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0004298	ORPHA:26790	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0005214	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26790	Pseudomyxoma peritonei		HP:0100790	ORPHA:26790	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001252	ORPHA:26791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001943	ORPHA:26791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003236	ORPHA:26791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003326	ORPHA:26791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003701	ORPHA:26791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0009020	ORPHA:26791	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000118	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000260	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000348	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000377	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000506	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000924	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001250	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001284	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001410	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001627	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001635	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001942	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001987	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002013	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002015	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002094	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002240	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002614	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002878	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002910	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003128	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003150	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003202	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003219	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003234	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003307	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003344	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003546	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003551	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003648	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0005280	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0011968	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0012240	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0025435	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0030199	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0045045	ORPHA:26791	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000078	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000113	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0000256	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001298	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001638	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0001735	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002091	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002171	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002282	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002421	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0002540	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003201	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0003691	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0006543	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0006582	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26791	Multiple acyl-CoA dehydrogenase deficiency		HP:0011675	ORPHA:26791	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001508	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001942	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0003219	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0008947	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0011968	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0012758	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0045045	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0410153	ORPHA:26792	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0000708	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0000750	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001250	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001254	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001332	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001397	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001638	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001999	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0002098	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0003198	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0006929	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0012734	ORPHA:26792	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0000252	ORPHA:26792	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0000648	ORPHA:26792	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001276	ORPHA:26792	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:26792	Short chain acyl-CoA dehydrogenase deficiency		HP:0001511	ORPHA:26792	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000008	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000035	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000164	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000327	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000365	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000498	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000499	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000518	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000534	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000600	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000668	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000670	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000679	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000704	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000819	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000939	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000975	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0000982	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001034	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001053	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001231	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001263	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001394	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001399	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001511	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001596	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001744	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001873	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001874	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001903	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0001928	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002024	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002205	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002216	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002240	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002514	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002575	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002650	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002664	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002665	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002745	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002757	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0002894	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0004322	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0005374	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0005528	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0008065	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0008066	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0008070	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0008404	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0008661	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0010450	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0010624	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0010885	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0011364	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0012732	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0012733	ORPHA:1775	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0100585	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0100627	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0100670	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0200037	ORPHA:1775	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1775	Dyskeratosis congenita		HP:0200042	ORPHA:1775	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0410020	ORPHA:468726	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0003614	ORPHA:468726	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0000712	ORPHA:468726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0031467	ORPHA:468726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0031469	ORPHA:468726	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0000716	ORPHA:468726	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0000718	ORPHA:468726	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0000739	ORPHA:468726	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0008770	ORPHA:468726	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:468726	Severe primary trimethylaminuria		HP:0011999	ORPHA:468726	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000028	ORPHA:1772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0004322	ORPHA:1772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0008968	ORPHA:1772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0012741	ORPHA:1772	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000027	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000033	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000047	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000054	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000061	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000062	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000808	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000812	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000837	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0003251	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0008689	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0100779	ORPHA:1772	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000039	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000041	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000045	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000048	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000077	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000085	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000150	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000218	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000286	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000347	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000365	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000358	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000403	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000465	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000505	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000639	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000729	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000767	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000771	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000821	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0000823	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001087	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001256	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001513	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001647	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001649	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001657	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001680	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0001822	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0002162	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0002164	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0002442	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0002650	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0002750	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0002967	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0006610	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0010044	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0010464	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0010743	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0012861	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0012887	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0030079	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0030680	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1772	45,X/46,XY mixed gonadal dysgenesis		HP:0040171	ORPHA:1772	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000069	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000133	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000147	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000175	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000286	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000288	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000358	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000413	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0000494	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0001156	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0001176	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0001256	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0001537	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0001629	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0002000	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0002750	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0004322	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0004422	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0004467	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0007598	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0008551	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0008678	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0010720	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0011304	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0011342	ORPHA:1770	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1770	XY type gonadal dysgenesis-associated anomalies syndrome		HP:0100335	ORPHA:1770	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0001251	ORPHA:370022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0002198	ORPHA:370022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0002342	ORPHA:370022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0002350	ORPHA:370022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0007033	ORPHA:370022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0100543	ORPHA:370022	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000486	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000545	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000646	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000657	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0001105	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0001263	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0002363	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0007068	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0011933	ORPHA:370022	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000540	ORPHA:370022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000556	ORPHA:370022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000639	ORPHA:370022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0001252	ORPHA:370022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0002599	ORPHA:370022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0003236	ORPHA:370022	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		HP:0000750	ORPHA:370022	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0002027	ORPHA:79273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0003163	ORPHA:79273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0010472	ORPHA:79273	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0000987	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0002018	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0002460	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0002572	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0008994	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0008997	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0009763	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0010473	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0011121	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0012217	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0040319	ORPHA:79273	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0000112	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0000709	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0000992	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0001030	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0001250	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0001402	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0001649	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0002093	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0002902	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0003418	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0005325	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0007178	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0008066	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0008528	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0009937	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0012850	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria		HP:0032936	ORPHA:79273	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria	NOT	HP:0001903	ORPHA:79273	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79273	Hereditary coproporphyria	NOT	HP:0001945	ORPHA:79273	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002027	ORPHA:79276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0003163	ORPHA:79276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0010473	ORPHA:79276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0012217	ORPHA:79276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0012379	ORPHA:79276	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000083	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000822	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001268	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001649	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002017	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002019	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0003418	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0006824	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0009763	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0009830	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0030833	ORPHA:79276	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000711	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000716	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000738	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000739	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001250	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001262	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001289	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001402	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001945	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002014	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002093	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002203	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002354	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002460	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002595	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0002902	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0003270	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0003474	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0004347	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0007002	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0007024	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0007178	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0008994	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0008997	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0011999	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0040319	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0100785	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0410263	ORPHA:79276	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000016	ORPHA:79276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000020	ORPHA:79276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0000975	ORPHA:79276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001259	ORPHA:79276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0001337	ORPHA:79276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria		HP:0100518	ORPHA:79276	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79276	Acute intermittent porphyria	NOT	HP:0011121	ORPHA:79276	TAS					P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0007537	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0008066	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001030	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0040320	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001878	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0012804	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0100699	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0030756	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001790	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001072	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0000953	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001010	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0002219	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0033009	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0003401	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0000989	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0000969	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0011273	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0004447	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001923	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0020181	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0008282	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0500115	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001744	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001882	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001873	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001892	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0000618	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0100532	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0500046	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001096	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0000656	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0000938	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0100512	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0001560	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0040322	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0200041	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0005406	ORPHA:79277	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0011457	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0004552	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0002797	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0000939	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0012132	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0008069	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0002860	ORPHA:79277	TAS		HP:0040284			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0012187	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0010472	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0012217	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0010473	ORPHA:79277	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79277	Congenital erythropoietic porphyria		HP:0009025	ORPHA:79277	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000098	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000175	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000243	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000275	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000276	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000286	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000347	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0000474	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0001249	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0001252	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0001347	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1779	Dysmorphism-cleft palate-loose skin syndrome		HP:0001582	ORPHA:1779	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0000964	ORPHA:79278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0000969	ORPHA:79278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0000989	ORPHA:79278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0000992	ORPHA:79278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0001081	ORPHA:79278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0001394	ORPHA:79278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0001410	ORPHA:79278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0001935	ORPHA:79278	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0010472	ORPHA:79278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79278	Autosomal erythropoietic protoporphyria		HP:0010783	ORPHA:79278	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000028	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000049	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000239	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000286	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000303	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000316	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000319	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000369	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000411	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000431	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000494	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000506	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0000508	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0001256	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0001537	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0001608	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0001928	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0002162	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0002167	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0002857	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0002967	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0003764	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0001382	ORPHA:1778	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1778	Facial dysmorphism-shawl scrotum-joint laxity syndrome		HP:0010669	ORPHA:1778	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0000365	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0000486	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0000639	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0000648	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0000717	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0000763	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0000962	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001004	ORPHA:79279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001009	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001250	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001252	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001257	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001263	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001324	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001336	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0001639	ORPHA:79279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0002071	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0002240	ORPHA:79279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0002321	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0002363	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0002376	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0003401	ORPHA:79279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0003700	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0004374	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0007256	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0007360	ORPHA:79279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0009830	ORPHA:79279	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0010864	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0100585	ORPHA:79279	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:79279	Alpha-N-acetylgalactosaminidase deficiency type 1		HP:0100704	ORPHA:79279	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0007029	ORPHA:231160	TAS		HP:0040280			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0000822	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0001123	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0001250	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0001269	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0002326	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0002363	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0002621	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0012518	ORPHA:231160	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0002138	ORPHA:231160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0002170	ORPHA:231160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0002616	ORPHA:231160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0002647	ORPHA:231160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0012246	ORPHA:231160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:231160	Familial cerebral saccular aneurysm		HP:0040197	ORPHA:231160	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000316	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000567	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000612	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0001156	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0001249	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0001263	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0001831	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0007370	ORPHA:1777	TAS		HP:0040281			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000256	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000268	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000276	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000280	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000347	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000369	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000444	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0001763	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0002970	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0004942	ORPHA:1777	TAS		HP:0040282			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000174	ORPHA:1777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000179	ORPHA:1777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000324	ORPHA:1777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000506	ORPHA:1777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0000568	ORPHA:1777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0004209	ORPHA:1777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]
ORPHA:1777	Temtamy syndrome		HP:0001382	ORPHA:1777	TAS		HP:0040283			P	ORPHA:orphadata[2025-10-22]